Species Accounts - BIRDS
American bittern (Botaurus lentiginosus)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
American bittern (Botaurus lentiginosus)
Status:
State: None
Federal: Species of Management Concern; Partners in Flight Priority Bird Species
GROUP DESIGNATION AND RATIONALE
Group 2
The American bittern is sparsely-distributed throughout the MSHCP Plan Area within its suitable habitat, however, it is not predictably distributed within all suitable areas. It is found in margins surrounding open water bodies, and freshwater marshes where emergent vegetation is present. There are several likely Core Areas for this species based on past use by the American bittern or presence of suitable habitat, including Mystic Lake/San Jacinto Wildlife Area, Santa Ana River/Prado Basin, and Collier Marsh. The breeding locations (possibly at Mystic Lake/San Jacinto Wildlife Area [Garrett and Dunn 1980] and Santa Ana River/Prado Basin [L. Hays, pers. obs.]) which have been documented as active or possible are located at specific sites that require conservation. Because it is well known for using emergent habitat but has specific breeding location requirements, it is anticipated that this species will respond to a landscape level of management with site specific requirements.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 410 acres of suitable nesting and foraging habitat for the American bittern consisting of freshwater marsh.
Objective 2
Include within the MSHCP Conservation Area at least 3 Core Areas including Mystic Lake/San Jacinto Wildlife Area (Subunit 4 of RecheCanyon/Badlands Area Plan; 2,690 acres), a possible nesting area, Santa Ana River/Prado Basin (9,670 acres), a known nesting area, and Collier Marsh (Proposed Linkage 2; 160 acres), a potential nesting area, as well as other suitable habitat locations at Lake Skinner/Diamond Valley Lake (Existing Core J; 24,370 acres), Lake Mathews (Existing Core C; 15,610 acres), Vail Lake (Subunit 3 of Southwest Area Plan; 12,320 acres), Temescal Wash (Subunit 3 of Temescal Canyon Area Plan; 4,010 acres), and Temecula Creek (Subunit 2 of Southwest Area Plan; 850 acres).
Objective 3
A 100-meter buffer will be established around emergent vegetation areas identified in Objective 2 as they are incorporated into the MSHCP Conservation Area.
Objective 4
Within the MSHCP Conservation Area, maintain (once every 8 years) the continued use of 50 percent of the Core Areas.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
The American bittern is virtually restricted to dense beds of cattails and rushes within freshwater and brackish water systems (Garrett and Dunn 1988). For the purpose of the conservation analysis, potential habitat for the American bittern includes freshwater marsh habitat. In addition, although not quantified, potential habitat includes the margins surrounding open water bodies that may contain desirable emergent plant communities suitable for foraging and nesting opportunities. Based on these habitats, the Plan Area supports approximately 470 acres of potential habitat for the American bittern. Table 1 shows the conservation and loss of potential habitat for the American bittern. Overall, approximately 410 acres ( 87 percent) of potential habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public Lands.
TABLE 1
SUMMARY OF HABITAT CONSERVATION FOR
AMERICAN BITTERN
| Vegetation Type | MSHCP Plan Area (Acres) | Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) | Public/ Quasi-Public (Acres) | Total Within MSHCP Conservation Area (Acres) | Rural/ Mountainous (Acres) | Outside MSHCP Conservation Area (Acres) | Total Outside MSHCP Conservation Area (Acres) | ||
| TOTAL | 470 | 170 (36%) | 240 (51%) | 410 (87%) | 0 (0%) | 60 (13%) | 60 (13%) |
| All Bioregions | |||||||
| Freshwater Marsh | 470 | 170 | 240 | 410 | 0 | 60 | 60 |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
The Riparian/Riverine Areas and Vernal Pools policy described in Section 6.1.2 of the MSHCP, Volume 1, provides for conservation of wetlands and riparian values which will protect some habitat as well as important hydrologic functions for this species through avoidance and minimization. Mitigation for impacts to wetlands shall be incorporated in accordance with the "No Net Loss" policy of federal and state wetland regulations. The proposed mitigation shall be directly related to the functions and values of the wetland as related to this species and result in equivalent replacement.
As described below under Data Characterization, six of the eight recent point localities have a high location precision. Of these six point localities, all will be inside the Criteria Area or Public/Quasi-Public Lands. In addition, the one known nesting and one possible nesting location are within the Criteria Area or Public/Quasi-Public Lands. Also, the Core Area at Collier Marsh is within the Criteria Area or Public/Quasi-Public Lands. The other potential areas that contain suitable habitat, Lake Skinner (Existing Core J; 24370 acres), Lake Mathews (Existing Core C; 15610 acres), Vail Lake (Subunit 3 of Southwest Area Plan; 12,320 acres), Temescal Wash (Subunit 3 of Temescal Canyon Area Plan; 4,010 acres), and Temecula Creek (Subunit 2 of Southwest Area Plan; 850 acres), also are within the Criteria Area or Public/Quasi-Public Lands. Conservation of this species will be from a landscape perspective because the species is relatively difficult to detect yet has specific habitat requirements. Additionally, there are definable locations for focusing conservation efforts, and there are two important locations for breeding that are essential for conservation for the species.
MSHCP Conservation Area Configuration Issues
Several areas of emergent habitat that contain the current known nesting locations, possible nesting locations, and potential foraging and nesting locations of the American bittern will be conserved in the Criteria Area and Public/Quasi-Public designations including the Prado Basin/Santa Ana River, Mystic Lake/San Jacinto Wildlife Area, Collier Marsh, Lake Skinner, Lake Mathews, Vail Lake, Temescal Wash, and Temecula Creek. Additionally, as these areas are incorporated into the MSHCP Conservation Area the margins surrounding these open water areas will be included in the MSHCP Conservation Area as well. As identified above, the species occurs within the MSHCP Plan Area predominantly as a transient or migrant and, as such, the MSHCP Conservation Area will provide adequate habitat for foraging during nomadic visits to the area and migratory stopovers as well as habitat containing potential nest sites with adequate protection around each nest site and foraging areas during the breeding season. Foraging areas are provided in suitable locations at Vail Lake, Lake Skinner, Mystic Lake/San Jacinto Wildlife Area, Collier Marsh, Lake Mathews, and Prado Basin/Santa Ana River. Potential and likely nest sites are provided in the Mystic Lake/San Jacinto Wildlife Area and known nesting areas are provided in the Prado Basin/Santa Ana River. These MSHCP Conservation Area areas are linked as well, however the American bittern, due to its ability to move long distances and nomadically, may rely less on the linkage than other species.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 410 acres of suitable Conserved Habitat including freshwater marsh and the three Core Areas (including the two known or possible nest sites within the Prado Basin/Santa Ana River, Mystic Lake/San Jacinto Wildlife Area, and Collier Marsh) as well as the suitable locations at Lake Skinner, Lake Mathews, Vail Lake, Temescal Wash, and Temecula Creek. The current population size of the American bittern is unknown due to its very secretive nature.
INCIDENTAL TAKE
About 60 acres (approximately 13 percent) of potential habitat for the American bittern will be outside the Criteria Area and Public/Quasi-Public areas and individuals within these areas will be subject to Incidental Take consistent with the Plan. Not-conserved habitat includes the margins surrounding Hemet Lake and Lake Riverside. Covered activities in these areas will be subject to the Protection of Species Associated with Riparian/Riverine Areas and Vernal Pools policy included in Section 6.1.2, Volume I of the MSHCP which calls for avoidance and minimization of impacts to wetlands.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The UCR location database contains a total of 18 records dated from 1900 to 1999. A total of eight of these records are recent, (within the past 10 years) and six of these recent records are precise records and could be accurately located within the Plan Area. The habitat types for these records include alkali playa, riparian, marsh, chaparral, and sage scrub, as well as one residential habitat record. This residential record may either no longer be extant or could have been located within a localized marsh within a residential development. Overall, the database records indicate that the American bittern is present within the Plan Area but in relatively low numbers.
The amount of literature available for the American bittern is relatively low. The species is secretive and located within a habitat within which it is difficult to conduct surveys and studies. The literature contains general biology information and some population studies and very little is available for the Plan Area other than general distribution studies.
Habitat and Habitat Associations
American bitterns in California are found almost exclusively in emergent habitat of freshwater marshes and vegetated borders of ponds and lakes (Grinnell and Miller 1944). It may occur in sparsely vegetated wetlands occasionally and in tidal marshes rarely (Gibbs et al. 1992). It usually hides, rests, and roosts solitarily amidst tall, dense, emergent vegetation, on the ground, or near the ground on a log, stump, or on emergent plants. It does not normally perch in trees. It feeds in marshes, meadows, and along the edges of shallow ponds (Terres 1980). It also nests within emergent marshes within cattails, cordgrass, sedges, grasses, sedges of a wet meadow or marsh (Terres 1980). It will inhabit wetlands of all sizes but is more abundant on larger wetlands and may prefer impoundments and beaver-created wetlands to wetlands of glacial origin.
Biogeography
American bitterns breed locally from southeastern Alaska eastward to Newfoundland southward to southern California and Virginia; they have also bred (at least formerly) on the Mexican plateau. The species winters from British Columbia eastward to northern Florida south through (at least) Mexico and Cuba (AOU 1998).
The dependence on inland, freshwater marshlands suggests that this species may be a relict over much of the U.S. Historically, the range may have shifted northward, tracking the distribution of wetlands created by retreating glaciers. Breeding Bird Survey sighting frequencies indicate this species is more abundant in Canada than in the U.S., declining sharply below the northern border states. Thus it may be adapted primarily to northern climates and wetlands and now occurs sparsely in the U.S. over what represents the southern edge of its breeding range. Population declines in the U.S. may represent a hastening of an ongoing northern retreat by the species, in part because of habitat destruction in the southern portion of its range (Gibbs et al. 1992).
Zeiner. et al. (1990) describe the distribution, abundance, and seasonality as follows: the American bittern is distributed widely in winter in fresh emergent wetlands, primarily west of the Sierra Nevada. In the Central Valley, it is fairly common October to April, and uncommon to rare the rest of the year; although it breeds there. It is less common on the coastal slope, and no longer breeds regularly south of Monterey County (Garrett and Dunn 1981). In Imperial Valley and along Colorado River, it is fairly common October to April, rare through the summer, and may breed at the northern end of the Salton Sea. In the northeast plateau and east of the Sierra Nevada crest south to Lake Tahoe, it is rare from May to August; it breeds locally. It is rare August to May in saline emergent wetlands along the coast. Elsewhere in the lowlands, it is a rare transient and local winter resident (Cogswell 1977, McCaskie, et al. 1979, Garrett and Dunn 1981). Within coastal southern California, the species is primarily a winter visitor, with nesting occurring only rarely in the coastal plain (Garrett and Dunn 1981).
The small breeding population in the lowlands may be nonmigratory; it may be augmented during October to April by migrants, probably from north of California and from the northeastern plateau, which is deserted in winter by this species (Zeiner, et al. 1990).
Known Populations Within Western Riverside County
Although American bitterns have been repeatedly recorded in the San Jacinto Wildlife Area/Mystic Lake area and it possibly breeds there (Garrett and Dunn 1981) the only known breeding location is at the Prado Basin (L. Hays, pers. comm.).
Geographic locations recorded within the U.C. Riverside database include: Temecula Creek, Temescal Wash, Lake Mathews, Santa Ana River/Prado Basin, Lake Elsinore, Lake Perris, and Mystic Lake/San Jacinto Wildlife Area. These records do not confirm breeding locations but the habitat is present and breeding could occur in these regions or the area may be used for foraging. American bitterns are secretive birds and may escape detection in the absence of relatively intensive, focused surveys.
Biology
Genetics: The American bittern is the smallest of the four species of Botaurus bitterns. Within the genus, the American bittern and south American bittern differ sufficiently in skeletal characteristics from one another and from the old world bitterns to be considered separate species (Gibbs et al. 1992). The species is monotypic and available data do not support the subspecific differentiation of birds from the eastern versus western North America (Gibbs et al. 1992).
Diet and Foraging: The American bittern forages within the emergent vegetation and shallow water of fresh or saline wetlands (Zeiner, et al. 1990). It feeds less often in adjacent shallow water of lakes, backwaters of rivers, or estuaries; and occasionally along adjacent shores. It feeds most actively at dusk or at night (Terres 1980), but also apparently at any time of day. It stands motionless and waits for prey, or stalks very slowly; it grasps the prey in the bill with a quick strike (Kushlan 1976b). It eats mainly insects, amphibians, fish, crayfish, and small mammals; also snakes, miscellaneous invertebrates, and birds.
Daily Activity: The American bittern is a year-long, circadian feeder, but most activity is crepuscular and nocturnal (Zeiner, et al. 1990).
Reproduction: The nest of the American bittern is a platform of matted, emergent aquatics, other herbaceous stems, sticks and/or leaves, usually in shallow water, but sometimes floating, or on the ground. It nests within the emergent vegetation and shallow water of fresh or saline wetlands (Zeiner, et al. 1990). Within the Prado Basin, the birds possibly breed in ponds with substantial tule/bulrush cover (L. Hays, USFWS, pers. obs.). The timing of courtship and nest-building is unknown; eggs or young have been reported April to July (Cogswell 1977). It is possibly polygamous, based on minimal evidence. It is basically a solitary nester, but is often in the vicinity of other pairs. The clutch size is usually 3-5 eggs, with a range of 2-6 eggs. It is apparently single-brooded. Incubation is about 24 days. The semi-altricial, downy hatchlings are apparently tended solely by the female, and remain in the nest about two weeks.
Survival: Little information is available. One banded individual of the American bittern lived at least 8 years (Gibbs et al. 1992).
Dispersal: Ages at first flight, independence, and first breeding of the American bittern are unknown (Palmer 1962). The American bittern is thought to undergo extensive, postbreeding dispersal which may account for the number of sightings, mostly in September through December in locations as distant as Iceland, Norway and Great Britain (Gibbs et al. 1992).
Socio-Spatial Behavior: In a slough in Saskatchewan, less than 16 hectares (40 acres) in extent, there were five nests of the American bittern (Bent 1926). Distances between nests have been as little as 18 meters (57 feet) in Michigan (Middleton 1949), 37 meters (120 feet) in lowa (Provost 1947), and 46 meters (150 feet) in Minnesota (Vesall 1940). The territory is probably used mainly for courtship, copulation, and nesting; size is unknown (Palmer 1962).
Community Relationships: No information is available within the literature.
Threats to Species
American bitterns apparently historically were more common and widespread in coastal southern California (Garrett and Dunn 1981). As early as the 1940's, Grinnell and Miller (1944) noted that the "extent of distribution and numbers have been diminishing concurrently with the effacement of appropriate habitat." The population has declined due to the draining of marshes, human disturbance, and pesticides. Overgrazing of emergent vegetation also is detrimental to the species. (Arbib 1979).
Special Biological Considerations
American bitterns have been known to nest within restored bulrush marsh areas, a floodwater storage pool and even various kinds of upland vegetation, although this is rare (Svedarsky 1992). The species may also make use of wetlands created by surface mining (Perkins and Lawrence 1985).
Habitat degradation is also a factor in causing changes in the population size of the American bittern. Eutrophication, siltation, chemical contamination, and human disturbance may seriously reduce habitat quality, primarily by damaging the prey supplies. Changes in wetland isolation and stabilized water regimes may seriously erode habitat quality for bitterns (Gibbs et al. 1992).
Preservation of freshwater wetland habitats, particularly large (greater than 10 hectares) shallow wetlands with dense growths of robust emergents is the most urgent management need. Wetlands used for breeding by American bitterns also need to be protected from chemical contamination, siltation, eutrophication, and other forms of pollution that harm the birds or their food supplies (Gibbs et al. 1992).
LITERATURE CITED
Arbib, R. 1979. The blue list for 1980. American Birds 33: 830-835.
AOU (American Ornithologists' Union). 1998. Check-List of North American Birds. Seventh Edition. American Ornithologists' Union, Washington, D.C. 829 pp.
Bent, A. C. 1926. Life histories of North American marsh birds. U.S. Natl. Mus. Bull. 135. 490pp.
Cogswell, H. L. 1977. Water birds of California. Univ. California Press. Berkeley 399 pp.
Garrett, K. and J. Dunn. 1981. Birds of Southern California: Status and Distribution. Los Angeles Audubon Society. 407 pp.
Gibbs, J.P., S. Melvin, and F. A. Reid. 1992. American Bittern. The Birds of North America 18: 1-12.
Grinnell, J. and A.H. Miller. 1944. The Distribution of the Birds of California. Pacific Coast Avifauna Number 27. Copper Ornithological Club, Berkeley, California. Reprinted by Artemisia Press, Lee Vining, California; April, 1986. 617 pp.
Kushlan, J. A. 1976b. Wading bird predation in a seasonally fluctuating pond. Auk 93:464- 476.
McCaskie, G., P. De Benedictis, R. Erickson, and J. Morlan. 1979. Birds of northern California, an annotated field list. 2nd ed. Golden Gate Audubon Soc., Berkeley. 84pp.
Middleton, D. S. 1949. Close proximity of two nests of American bitterns. Wilson Bull. 61:113.
Palmer, R. S., ed. 1962. Handbook of North American birds. Vol. 1. Yale University Press, New Haven, CT. 567pp.
Perkins, G. A. And J. S. Lawrence. 1985. Bird use of wetlands created by surface mining. Trans. Ill. State Acad. Sci. 78: 87-96.
Provost, M. W. 1947. Nesting of birds in the marshes of northwest Iowa. Am. Midl. Nat. 38:485-503.
Sverdarsky, W. D. 1992. Observations on nesting of the American bittern in northwest Minnesota. Prairie Naturalist 24: 241-250.
Terres, J. K. 1980. The Audubon Society encyclopedia of North American birds. A. Knopf, New York. 1100pp.
Vesall, D. B. 1940. Notes on nesting habits of the American bittern. Wilson Bull. 52:207- 208.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
bald eagle (Haliaeetus leucocephalus)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
bald eagle (Haliaeetus leucocephalus)
Status:
State: Endangered; Fully-Protected Species; California Department of Forestry and Fire Prevention Sensitive
Federal: Threatened (Federal Register 60:36010, July 12, 1995); Partners in Flight Priority Bird Species; Bald Eagle Protection Act of 1940
The bald eagle was initially listed on February 14, 1978 as an endangered species throughout the lower 48 states, except in Minnesota, Michigan, Wisconsin, Washington, and Oregon, where it was listed as a threatened species. On July 12, 1995, the USFWS announced that the bald eagle would be reclassified from endangered to threatened in the lower 48 states, effective August 11, 1995. In those states where the species was already listed as threatened, it remains classified that way but was proposed for delisting in July 1999.
GROUP DESIGNATION AND RATIONALE
Group 1
The bald eagle has a wide distribution throughout the MSHCP Plan Area within its suitable habitat. It occurs or has occurred at every open water body within the Plan Area. It uses suitable habitat predictably and responds well to available suitable habitat. It occurs within the Plan Area predominantly as a winter visitor with casual occurrences in the summer of individuals that have lingered at the wintering sites. It has attempted to breed at Lake Elsinore and at Lake Skinner but has not done so successfully.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 10,340 acres of open water habitat at the following seven open water bodies and one drainage: Lake Mathews, Diamond Valley Lake, Lake Skinner, Lake Elsinore, Vail lake, Lake Perris, Mystic Lake and Santa Ana River. Include within the MSHCP Conservation Area 5,520 acres of suitable riparian habitat within the Prado Basin and Santa Ana River.
Objective 2
A 100-meter buffer will be established around open water bodies identified in Objective 1 as they are incorporated into the MSHCP Conservation Area.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
For the purpose of the conservation analysis, potential habitat for the bald eagle includes open water lakes and reservoirs, a shoreline buffer of 100 meters around each of the open water lakes and reservoirs, and the riparian habitat within the Prado Basin and Santa Ana River. Although the bald eagle has not recently bred successfully within the MSHCP Plan Area, potential breeding habitat does occur around several of the water bodies. Based on these habitats, the Plan Area supports approximately 18,000 acres of potential habitat for the bald eagle. Table 1 shows the conservation and loss of potential habitat for the bald eagle. Overall, approximately 15,860 acres (88 percent) of potential habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public lands.
As described below under Data Characterization, 8 of the 17 recent point localities have a high location precision. Of these eight point localities, three will be inside the Criteria Area or Public/Quasi-Public Lands. However, of the five points located outside these habitat areas, all are mapped in existing residential/urban/exotic areas or in existing agriculture or other upland habitats. These habitats do not constitute suitable habitat but these locations may have been of a bird flying overhead or within habitat adjacent to one of the reservoirs. Conservation of this species is being considered from a landscape perspective because the species is found throughout the Plan Area and is well documented for the type of habitat within which they forage. While there are definable locations for focusing conservation efforts, these do not constitute Core Areas. Any nesting locations identified will be important to preserve.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
BALD EAGLE
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| All Bioregions | |||||||
| Open Water | 12,210 | 1,190 | 9,150 | 10,340 | 40 | 1,830 | 1,870 |
| Riparian Habitat within Prado Basin/Santa Ana River | 5,790 | 510 | 5,010 | 5,520 | 0 | 270 | 270 |
| TOTAL | 18,000 | 1,700 (9%) |
14,160 (79%) |
15,860 (88%) |
40 (<1%) |
2,100 (12%) |
2,140 (12%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
MSHCP Conservation Area Configuration Issues
Several large blocks of habitat supporting the current known locations and potential foraging and nesting locations of the bald eagle will be conserved as Criteria Area and Public/Quasi-Public designations, including the Prado Basin, Santa Ana River, Lake Skinner, Diamond Valley Lake, Lake Mathews, Lake Perris, Mystic Lake, Lake Elsinore, and Vail Lake. The MSHCP Conservation Area will provide adequate habitat for foraging during winter, nomadic visits to the area, and migratory stopovers. The MSHCP Conservation Area will also provide potential nest sites and foraging areas during the breeding season. Foraging areas are provided at Vail Lake, Lake Skinner, Diamond Valley Lake, Lake Perris, Mystic Lake, Lake Elsinore, Lake Mathews, Prado Basin and Santa Ana River. Potential perching and nest sites are provided at these open water/reservoir areas in the form of large trees or snags within the 100 meter wide buffer around each water body. The bald eagle, due to its ability to move long distances, will rely less on the linkages between potential breeding areas than other species.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 15,860 acres of suitable Conserved Habitat including open water bodies and riparian habitat within the Santa Ana River and Prado Basin. The current population size of the bald eagle is unknown because it is primarily a winter and transient visitor. However, a single pair has made repeated, but unsuccessful, attempts to breed at Lake Skinner in recent years.
INCIDENTAL TAKE
The estimated Take of the bald eagle is based on the acreage of potentially suitable and/or occupied habitat. About 2,140 acres (12 percent) of potential habitat for the bald eagle will be outside the Criteria Area and Public/Quasi-Public designations and individuals within these areas will be subject to Incidental Take consistent with the Plan. Potential habitat not included within the MSHCP Conservation Area includes the open water habitat at Hemet Lake and Lake Riverside.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The UCR location database for the bald eagle includes a total of 31 records dated from 1973 to 1999. All but one of these records is from local biologists reports; a survey conducted in 1996 by the USFWS reported one location record. A total of 17 of these records are relatively recent (within the past 10 years) and of these recent records, a total of 8 are of high precision. The habitats with which these records are associated includes grassland, chaparral, riparian, croplands, residential, and open water. The upland and residential habitat location records probably reflect observations of a bald eagle in flight over an area.
The literature available on the bald eagle is fairly extensive for a number of reasons, not the least of which is the fact that the bald eagle is our Nation's symbol. It has been studied for many years by ornithologists interested in raptors. Due to its listed status, the pesticide problems to which were attributed its population decline a number of years ago, as well as the interest in its recovery from its population decline, a large number of natural history articles as well as summary information within the general ornithological literature is available. Little information is available that pertains directly to the Plan Area other than general distribution information.
Habitat and Habitat Associations
Range-wide, bald eagles occur primarily at or near seacoasts, rivers, swamps, and large lakes (AOU 1998). It is considered a bird of aquatic ecosystems but within such areas, it must have an adequate food base, perching areas, and nesting sites to support them (Gerrard and Bortolotti 1988). Perching sites need to be composed of large trees or snags with heavy limbs or broken tops (USFS pers. comm. 1999). The bald eagle nests in trees, rarely on cliff faces and ground nests in treeless areas and always relatively close to water with suitable foraging opportunities. The actual distance to water varies within and among populations of the bald eagle. In some cases, the distance to water is not as critical as the quality of the foraging area. The quality of the foraging areas is defined by the diversity, abundance, and vulnerability of the prey base, the structure of aquatic habitat such as the presence of shallow water and absence of human development and disturbance (Buehler 2000). The diurnal perch habitat is characterized by presence of tall, easily accessible, often super-canopy trees adjacent to the shoreline foraging habitat. The perch tree species used by the bald eagle are highly variable, including both coniferous and deciduous species if present. Most perch trees are live trees although dead trees may be preferred if available. The bald eagle selects a wider range of tree species and sizes for perching than for nesting or roosting (Buehler 2000).
Within southern California, although birds are found in these same habitats, they are most often recorded at large deep inland bodies of water and are considered a winter resident that in the past may have bred in the area (Garrett and Dunn 1981). In winter, bald eagles often congregate at specific wintering sites that are generally close to open water and that offer good perch trees and night roosts. The bald eagle may roost communally in winter in dense, sheltered, remote conifer stands (Zeiner, et al. 1990). In Klamath National Forest, winter roosts were 16-19 kilometers (10-12 miles) from feeding areas (Spencer 1976). The bald eagle often concentrates in large numbers on the wintering grounds. The winter habitat suitability is defined by the food availability, the presence of roost sites that provide protection from inclement weather and absence of human disturbance although bald eagles will tolerate some human activity in areas of high prey availability. The perching habitat during the wintering season is characterized by the presence of tall trees located adjacent to foraging areas similar to other times of the year (Buehler 2000).
Biogeography
The bald eagle is the only sea eagle regularly occurring on the North American continent. Bald eagles breed locally from Alaska eastward to Newfoundland southward locally to Baja California, Sonora, Texas, and Florida. The species winters in the large majority of the breeding range but generally withdraws from central Alaska and the central and the northern portions of Canada (AOU 1998). Individuals that breed in California may make only local winter movements in search of food.
Within mainland southern California, the species primarily winters at larger bodies of water in the lowlands and mountains (Garrett and Dunn 1981). It is fairly common as a local winter migrant at a few favored inland waters in southern California. Largest numbers occur at Big Bear Lake, Cachuma Lake, Lake Mathews, Nacimiento Reservoir, San Antonio Reservoir, and along the Colorado River (Zeiner et al. 1990). Recent breeding attempts on the mainland south of Santa Barbara County (e.g., Silverwood Lake, Lake Skinner, Lake Perris) have been unsuccessful (K. Cleary-Rose, pers. comm., 2002).
The historic breeding range of the bald eagle is probably similar to the present breeding distribution with major changes, both losses and gains of breeding areas in the twentieth century. The distribution reported by Oberholser (1906) is very similar to the present distribution (Buehler 2000).
Known Populations Within Western Riverside County
Notwithstanding failed nesting attempts (see "Current Range" above) by summering or resident birds, the bald eagle is primarily a migrant and wintering species within western Riverside County. Although the species remains nowhere common and is generally rare and local in southern California (Garrett and Dunn 1981), the species could turn up virtually anywhere within western Riverside County in suitable habitats and may, in fact, attempt to nest. Thus, as a species occurring within the area in the summer, it is considered a casual occurrence. Generally, however, it is considered a very localized winter visitor that is fairly common at a few favored wintering sites around inland bodies of water yet is generally very rare otherwise (Garrett and Dunn 1981).
Birds have been detected in recent years at the Prado Basin, Lake Skinner, Lake Mathews, and Lake Perris. There are also records from Lake Elsinore, where the species may have bred in the past (Garrett and Dunn 1981), and the species has been observed infrequently at Lake Hemet and Vail Lake. Recently, the bald eagle has attempted to breed at Lake Skinner. Up to 20 eagles were reported to be present at Lake Mathews (Garrett and Dunn 1981).
Biology
Genetics: There are eight species in the genus Haliaeetus which are distributed worldwide except in South America. The genus is most closely related to the other fish eagles and is perhaps also related to the scavenging kites and to the Old World vultures. The bald eagle is likely most closely related to and may constitute a superspecies with the white-tailed eagle (H. Albicilla) (Buehler 2000).
Diet and Foraging: Fish predominate the typical diet of bald eagles, however, many other types of prey are also taken, including waterfowl and small mammals, and carrion especially in the wintering areas (USFWS 1995). It swoops from hunting perches, or soaring flight to pluck fish from water. It is also known to wade into shallow water to pursue fish. It may pounce on, or chase, injured or ice-bound water birds. In flooded fields, the species occasionally pounces on displaced voles, or other small mammals. Open, easily approached hunting perches and feeding areas are used most frequently (Zeiner, et al. 1990). Bald eagles tend to hunt cooperatively (Brown 1999). Studies of prey items in northern California, showed bald eagles do not differentiate between native and non-native freshwater fish species (Jackman, et al. 1999). One study of birds in Texas found them to eat a relatively equal proportion of birds, reptiles and fish (Mabie, et al. 1995). One wintering population in the lower Great Lakes basin was observed feeding on carcasses of white-tailed deer during 47 percent of observed feedings (Ewins and Andress 1995). The same group observed immature individuals feeding on garbage and offal 39 percent of feedings.
Daily Activity: Wintering bald eagles in New Mexico spent 95.3 percent of their time perched and 4.7 percent in flight (Zwank, et al. 1996). Of the time spent in flight, 13.0 percent was spent foraging (Zwank, et al. 1996). Winter feeding usually occurs immediately after dawn and in late afternoon (Zeiner, et al. 1990).
Reproduction: Breeding of the bald eagle occurs in open areas, near water, with nests often in large snags or old-growth trees (Brown 1999). The bald eagle also nests in a dominant live tree with open branch work, especially ponderosa pine. It nests most frequently in stands with less than 40 percent canopy, but there is usually some foliage shading the nest (Call 1978). It often chooses the largest tree in a stand on which to build its stick platform nest. The nest may be a massive structure, twelve feet high, eight and a half feet across and with a wet mass of decaying vegetation in the center, weighing many hundred pounds (Brown and Amadon 1968). The nest is typically located 16-61 meters (50-200 ft) above ground, usually below the tree crown. The species of tree that is used for locating the nest site is apparently not so important as the height and size. The nest is usually located near a permanent water source. In California, 87 percent of the nest sites of the bald eagle were within 1.6 kilometers (1 mile) of water. Individuals have been known to use the same nest for up to 35 years (Brown 1999).
The clutch size of the bald eagle is usually two, but can vary from one to three, and eggs are laid once annually (Brown 1999). The bald eagle breeds from February through July, with a peak in activity from March to June. Incubation of the eggs usually lasts 34-36 days. The semi-altricial young hatch asynchronously (Ehrlich, et al. 1988). The species is monogamous, and breeds first at 4-5 years (Zeiner, et al. 1990).
Survival: In one study of bald eagle nests in British Colombia, Canada, food supply was identified as the "key factor" in limiting breeding success (Elliot, et al. 1998). Because of the asynchronous hatching the older nestling may kill the younger, smaller sibling if the food supply is inadequate (Brown and Amadon 1968). The recorded longevity in the wild is 28 years and 36 years in captivity. Bald eagles may follow the survival pattern similar to other raptors with lower first-year survival followed by increasing survival to adulthood. Adult survival is high in most studies on survivorship (Buehler 2000).
Dispersal: The young of the bald eagle leave the nest 70 to 98 days after hatching but do not reach breeding age until four or five (Brown 1999). A mark-recapture study of a breeding population in Texas concluded that birds fledged there may disperse to breeding communities throughout the southern United States (Mabie, et al. 1994).
Socio-Spatial Behavior: The bald eagle home range of resident pairs on the Columbia River averaged 22 km2 for both breeding and non-breeding periods (Garrett, et al. 1993). The breeding territory in Alaska (n= 14), varied from 11-45 hectares (28-112 acres), and averaged 23 hectares (57 acres) (Hensel and Troyer 1964). The breeding territory is defended from the mating through the fledging period of the pair. Minimum distances between bald eagle nests were 1 kilometer (0.6 miles) in Alaska, and 17 kilometers (10 miles) in Washington (Zeiner, et al. 1990).
Community Relationships: The bald eagle competes with, and steals prey from osprey (Zeiner, et al. 1990). It has been observed causing a turkey vulture to disgorge its food (Brown and Amadon 1968).
Threats to Species
Habitat loss, the expressed effects of select pesticides on reproductive success, and persecution of the species necessitated the listing of the bald eagle. The use of DDT after World War II led to eggshell thinning which drastically reduced reproductive success and the species' populations (USFWS 1995). The species does not occupy its former breeding range in southern California or occur in numbers comparable to historical totals (Grinnell and Miller 1944 and Garrett and Dunn 1981). However, successful captive breeding efforts, the banning of certain organochlorine pesticides, and other recovery efforts have resulted in apparent, significant increases in eagle numbers on the continent. Special pressures on individuals in the southwestern United States include: heat stress, nest parasites and entanglement in fishing line debris from intense fishing pressure (USFWS 1995).
A study of nests in Oregon identified the following causes of nest failures: pesticides (32 percent), proximity to nearest-neighbor breeding pairs (11 percent), infertile eggs (7 percent), nestling mortality (3 percent), human disturbance (2 percent), changes in members of a pair (1 percent), and unknown causes (21 percent) (Anthony, et al. 1994).
Human recreational use of reservoirs and rivers occupied by bald eagles has been greatly studied (Stalmaster and Kaiser 1998). Territories have been abandoned after there has been disturbance from logging, recreational development, and other human activities near nests of the bald eagle (Thelander 1973). In northwest Washington, feeding activity was found to decline exponentially with increased recreational activity (Stalmaster and Kaiser 1998). Foot traffic caused the greatest flushing distance but boat activities accounted for a greater proportion of the disturbances (Stalmaster and Kaiser 1998).
Special Biological Considerations
Bald eagles are sensitive to human encroachment and disturbance. Currently, over one million dollars in public and private money is spent each year toward recovery and protection of bald eagle populations (USFWS 1995). These efforts have increased populations from 417 active nests in the lower 48 states in 1963, according to the National Audubon Society, to 4,450 in 1994 (USFWS 1995).
Researchers recommended that recreational activity during the breeding season be restricted during the first five hours of sunlight where bald eagles are present (Stalmaster and Kaiser 1998). Another study in Arizona found 22-times more eagles nesting in areas with low human use compared to areas with moderate or high human use (Brown and Stevens 1997).
The variable effects of human activity on the reproductive performance of bald eagles implies a threshold for detrimental impact between pristine isolation and outright destruction. Management concepts to protect nesting bald eagles have evolved from concentric-circles buffer zones at nest sites through single territory zonation to a multiple territory regional approach (Grubb and King 1991). Additional research has concluded that management of potentially disturbing human activity near breeding bald eagles should be based on multivariate considerations of action and reaction (Grubb and King 1991). Distance to disturbance is the most important aspect of human disturbance. Human activities that are distant, of short duration, out of sight, few in number, below, and quiet have the least impact. Despite the multi-dimensional nature of human disturbance, any category of disturbance can, in excess or under the proper circumstances, disrupt normal behavior or cause nesting failure. Importance of disturbance groups varies with their associated characteristics. This study suggests a minimum, generic, primary zone of approximately 600 meters around breeding bald eagles (Grubb and King 1991). A 1,200-meter secondary buffer zone would accommodate most of the distant responses from vehicle, noise, and aircraft disturbance. Typically, no human activity is permitted at any time within a primary protection zone. Within a secondary buffer zone, limited, nonpermanent activity may be allowed during the non-breeding season. Other buffer distances of similar magnitudes have been suggested by other researchers for breeding bald eagles (summarized in Grubb and King 1991). This study has provided additional specific distances based on the general category of the disturbance. These values will be useful for management purposes in the event that the bald eagles located within the western Riverside County area attempt to breed. The management recommendations from Grubb and King (1991) for buffer distances for specific activities in association with breeding bald eagles are as follows: Pedestrian disturbance - complete restriction at 543 meters; aquatic disturbance - restriction at 200 meters; vehicle disturbance - complete restriction at 450 meters and limited vehicular control at 850 meters; noise disturbance (includes gunshot and sonic booms) - restrictions within 1,000 meters but may need extending up to 2,000 meters; aircraft disturbance - exclusion within 625 meters and limited flights within 1,100 meters.
The bald eagle was one of four wintering raptor species shown to be sensitive to urbanization, having a threshold of approximately five to seven percent urbanization (Berry, et al. 1998). A group of researchers have used perch tree abundance and shoreline development measures to accurately predict numbers of bald eagles (Chandler, et al.1995).
Human disturbance activities may elicit various responses from wildlife and differences in persecution histories result in diverse wildlife responses to different activity types. The bald eagle is more likely to flush when approached by a human on foot than when approached by an automobile (Holmes et al. 1993). That a person approaching in plain view of a raptor elicits a stronger response than a person within an approaching vehicle suggests that humans approaching slowly are viewed as a greater disturbance than vehicles, which are moving rapidly and screen humans. Some bald eagles have demonstrated habituation to human presence. Wintering bald eagles show lower flushing responses along rivers and estuaries with high levels of recreational boating activity than along adjacent areas with little boating activity (Holmes et al. 1993). However these studies did not monitor the effects of the human disturbances on the reproductive success. Spatial buffer zones are commonly used to protect nesting sites from disturbance, however, buffer zones for wintering raptors also could be effective if placed around sensitive foraging areas. From this study, a buffer zone that would prevent flushing by approximately 90 percent of the wintering individuals of the golden eagle would be set at 300 meters (Holmes et al. 1993). Although this study did not specify the bald eagle and studies were not conducted for bald eagles, presumably the buffer distance for wintering bald eagles might be set for at least as great as the golden eagle until further research determines a different distance is more beneficial.
Because of the selectivity of roost sites by bald eagles (roost trees have greater diameter at breast height, more branching structure and are generally taller than randomly sampled trees) forest harvests should be conducted through selective thinning, prescribed fire and seeding with roost-like trees (Dellasala, et al. 1998).
LITERATURE CITED
AOU (American Ornithologists' Union). 1998. Check-List of North American Birds. Seventh Edition. American Ornithologists' Union, Washington, D.C. 829 pp.
Anthony, R. G., R. W. Frenzel, F. B. Isaacs and M. G. Garrett. 1994. Probable causes of nesting failures in Oregon's bald eagle population. Wildlife Society Bulletin 2:576-582.
Berry, M. E., C. E. Bock and S. L. Haire. 1998. Abundance of diurnal raptors on open space grasslands in an urbanized landscape. Condor 100: 601-608.
Brown, B. T. and L. E. Stevens. 1997. Winter bald eagle distribution is inversely correlated with human activity along the Colorado River, Arizona. Journal of Raptor Research 31:7-10.
Brown, N. L. 1999. World Wide Web-site: http://arnica.csustan.edu/esrpp/baldeg.htm.
Brown, L., and D. Amadon. 1968. Eagles, hawks and falcons of the world. 2 Vols. Country Life Books, London. 945pp.
Buehler, D. A. 2000. Bald Eagle (Haliaeetus leucocephalus). Number 506. In The Birds of North America, A. Poole and F. Gill, Eds. Cornell Laboratory of Ornithology and The Academy of Natural Sciences, Washington D.C.
Call, M. W. 1978. Nesting habits and survey techniques for common western raptors. U. S. Dep. Inter., Bur. Land Manage., Portland, OR. Tech. Note No. 316. 115pp.
Chandler, S. K., J.D. Fraser, D. A. Buehler and J. K. D. Seegar. 1995. Perch trees and shoreline development as predictors of bald eagle distribution on Chesapeake Bay. Journal of Wildlife Management 59:325-332.
Cleary-Rose, K. 2002. Pers. comm. U.S. Fish and Wildlife Service.
Dellasala, D. A., R. G. Anthony, T. A. Spies and K. A. Engel. 1998. Management of bald eagle communal roosts in fire-adapted mixed-conifer forests. Journal of Wildlife Management 62:322-333.
Elliot, J. E., I. E. Moul, K. M. Cheng. 1998. Variable reproductive success of bald eagles on the British Columbia coast. Journal of Wildlife Management 62:518-529.
Ewins, P.J. and R. A. Andress. 1995. The diet of bald eagles, Haliaeetus leucocephalus, wintering in the lower Great Lakes Basin, 1987-1995. Canadian Field-Naturalist 109:418-425.
Ehrlich, P. R., D. S. Dobkin, and D. Wheye. 1988. The birder's handbook. Simon and Schuster, New York. 785pp.
Garrett, K. and J. Dunn. 1981. Birds of Southern California: Status and Distribution. Los Angeles Audubon Society. 407 pp.
Garrett, M G., J. W. Watson and R. G. Anthony. 1993. Bald Eagle Home Range and Habitat use in the Columbia River Estuary. Journal of Wildlife Management 57:19-27.
Gerrard and Bortolotti. 1988. The bald eagle: haunts and habits of a wilderness monarch. Smithsonian Inst. Press, Washington, 177pp.
Grinnell, J. and A.H. Miller. 1944. The Distribution of the Birds of California. Pacific Coast Avifauna Number 27. Copper Ornithological Club, Berkeley, California. Reprinted by Artemisia Press, Lee Vining, California; April, 1986. 617 pp.
Grubb, T. G. and R. M. King. 1991. Assessing human disturbance of breeding bald eagles with classification tree models. J. Wildl. Management 55: 500-511.
Hensel, R. J., and W. A. Troyer. 1964. Nesting studies of the bald eagle in Alaska. Condor 66:282-286.
Holmes, T., R. L. Knight, and G. R. Craig. 1993. Responses of wintering grassland raptors to human disturbance. Wildlife Society Bulletin 21: 461-468.
Jackman, R. E., W. G. Hunt, J. M. Jenkins and P. J. Detrich. 1999. Prey of nesting Bald Eagles in northern California. Journal of Raptor Research 33:87-96.
Mabie, D. W., M. T. Merendino and D. H. Reid. 1995. Prey of nesting bald eagles in Texas. Journal of Raptor Research 29:10-14.
Mabie, D. W., M. T. Merendino and D. H. Reid. 1994. Dispersal of Bald Eagles Fledged in Texas. Journal of Raptor Research 28: 213-219.
Oberholser, H. C. 1906. The North American eagles and their economic relations. U.S. Dept. Agriculture Biol. Surv. Bull. 27, Washington, D. C.
Spencer, D. A., ed. 1976. Wintering of the migrant bald eagle in the lower 48 states. Natl. Agric. Chem. Assoc. Publ., Wash. DC. 170pp.
Stahlmaster, M.V. and J. L. Kaiser. 1998. Effects of recreational activity on wintering bald eagles. Wildlife Monographs 137: 1-46.
Thelander, C. G. 1973. Bald eagle reproduction in California, 1972-1973. Calif. Dept. Fish and Game, Sacramento. Wildl. Manage. Branch Admin. Rep. 73-5. 17pp.
United States Fish and Wildlife Service. 1995. Endangered and Threatened Wildlife and Plants; Final Rule to Reclassify the Bald Eagle from Endangered to Threatened in all of the Lower 48. Federal Register 50 CFR Part 17, v.60, n.133 July 12, 1995:35999-36010.
United States Forest Service (USFS). 1999. Pers. comm. Species accounts for threatened, endangered and sensitive wildlife species occurring in the San Bernardino National Forest.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
Zwank, P.J., B. L. Tarrant, R. Valdez and D. L. Clason. 1996. Wintering bald eagle populations and behavior in the middle Rio Grande Basin, New Mexico. Southwestern Naturalist 41:149-154.
Bell's sage sparrow (Amphispiza belli belli)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
Bell's sage sparrow (Amphispiza belli belli)
Status:
State: Species of Special Concern
Federal: Partners in Flight Priority Bird Species; Species of Management Concern; Federal Special Concern species
Other: Audubon Society California Watch List
GROUP DESIGNATION AND RATIONALE
Group 2
The Bell's sage sparrow is widely but sparsely distributed throughout the MSHCP Plan Area within suitable habitat in the Riverside lowlands, Santa Ana Mountains, Desert Transition and San Jacinto Foothills Bioregions. It is absent from higher elevation Bioregions. The Bell's sage sparrow occurs within several areas that appear to be Core Areas including Jurupa Mountains, Lake Mathews-Estelle Mountain, Wasson Canyon, Santa Rosa Plateau, Sedco Hills, Hogbacks, Lake Skinner/Diamond Valley Lake, Vail Lake/Wilson Valley/Aguanga, Tule Valley, Santa Rosa Hills, Lakeview Mountains, Lake Perris, Badlands, and Box Springs Mountains. However, none of these Core Areas contains large or dense populations of the Bell's sage sparrow. The Bell's sage sparrow is a year-round resident within the Plan Area. Because it is well known for using coastal sage scrub and chaparral habitats, occurs widely but sparsely and well scattered within these habitats in the Riverside lowlands, San Jacinto Foothills, Desert Transition, and Santa Ana Mountains Bioregions, but has specific locations that are Core Areas, it is anticipated that this species will respond well to a landscape level of management with site specific requirements.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 245,750 acres of suitable habitat for Bell's sage sparrow including coastal sage scrub, chaparral, and desert scrubs in Riverside lowland, Santa Ana Mountains, Desert Transition, and San Jacinto foothills Bioregions.
Objective 2
Include within the MSHCP Conservation Area at least 12 of 14 Core Areas and interconnecting linkages for Bell's sage sparrow. Core areas will include the Jurupa Mountains (Proposed Noncontiguous Habitat Block 2; 1,230 acres), Lake Mathews-Estelle Mountain (Existing Core C plus Proposed Extension of Existing Core 2; 23,710 acres), Wasson Canyon (Subunit 5 of Elsinore Area Plan; 2,320 acres), Sedco Hills (Proposed Linkage 8; 5,470 acres), Hogbacks (Proposed Core 2; 5,050 acres), Lake Skinner/Diamond Valley Lake (Existing Core C plus Proposed Extension of Existing Cores 5, 6, 7; 29,060 acres), Vail Lake/Wilson Valley/Aguanga (Proposed Core 7; 50,000 acres), Tule Valley, (Proposed Core 6; 4,290 acres), Lakeview Mountains (Proposed Noncontiguous Habitat Block 5; 7,150 acres), Lake Perris (Existing Core H; 17,470 acres), Badlands (Proposed Core 3; 24,920 acres), and Box Springs Mountains (Existing Noncontiguous Habitat Block A plus Proposed Constrained Linkage 8; 2,920 acres).
Objective 3
Include within the MSHCP Conservation Area habitat linkages between Core Areas and areas important for dispersal including the Jurupa Mountains, Reche Canyon, and San Timoteo Creek areas.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
Although the distribution and habitat use of the Bell's sage sparrow is very similar to that of the coastal California gnatcatcher and Southern California rufous-crowned sparrow, the Bell's sage sparrow differs from each of these species in several factors: it occurs at higher elevations similar to the Southern California rufous-crowned sparrow but different from the coastal California gnatcatcher, it occurs in the Desert Transition bioregion, it rarely or never uses grassland habitat except possibly for dispersal, and it is more sparsely scattered at lower populations levels throughout the MSHCP Plan Area. For the purpose of the conservation analysis, potential habitat includes coastal sage scrub, chaparral, and desert scrubs within the Riverside Lowlands, San Jacinto Foothills, Santa Ana Mountains, and Desert Transition Bioregions. Bell's sage sparrow is documented to use the sparse form of chaparral which is included within the broader category of chaparral for the Plan Area (Martin and Carlson 1998). The mapping for the Plan Area does not distinguish between sparse and dense forms of chaparral. Based on these habitats, the Plan Area supports approximately 423,190 acres of potential habitat for the Bell's sage sparrow. Table 1 shows the conservation and loss of potential habitat for the Bell's sage sparrow. Overall, approximately 245,750 acres (58 percent) of potential habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public lands for all the habitats combined.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
BELL'S SAGE SPARROW
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| Habitats within Riverside Lowlands, San Jacinto Foothills, Santa Ana Mountains, and Desert Transition Bioregions | |||||||
| Desert Scrubs | 7,940 | 3,440 | 1,170 | 4,610 | 40 | 3,290 | 3,330 |
| Coastal Sage Scrub | 148,220 | 45,550 | 32,750 | 78,300 | 25,790 | 44,130 | 69,920 |
| Chaparral | 267,030 | 55,750 | 107,090 | 162,840 | 47,350 | 56,840 | 104,190 |
| TOTAL | 423,190 | 104,740 (25%) |
141,010 (33%) |
245,750 (58%) |
73,180 (17%) |
104,260 (25%) |
177,440 (42%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
This species may occur within Forest Service lands for nesting and foraging within coastal sage scrub, and chaparral in the Santa Ana Mountains bioregion. Currently there are no database records within the Forest Service lands, however, based on the elevation and habitats available within the Cleveland National Forest, it is likely to occur within the area. The locations within the Forest Service lands are expected to be in coastal sage scrub and chaparral habitat within the Cleveland National Forest. Under the existing Forest Land Allocation plan, these potential locations or habitats generally are located within the Wildhorse and Coldwater roadless areas, San Mateo Canyon Wilderness Area and possibly the Tenaja and Verdugo Range Allotments.
As described below under Data Characterization, 98 of the 264 point localities have a high location precision. Of these 98 point localities, 34 (35 percent) will be inside the Criteria Area or Public/Quasi-Public lands. A total of 18 (18 percent) will be in the Rural/Mountainous zone. Of the 46 (47 percent) points located outside the MSHCP Conservation Area, 26 are mapped in existing residential/urban/ exotic areas.
Twelve of fourteen Core Areas will be conserved within the Jurupa Mountains (Proposed Noncontiguous Habitat Block 2; 1,230 acres), Lake Mathews-Estelle Mountain (Existing Core C plus Proposed Extension of Existing Core 2; 23,710 acres), Wasson Canyon (Subunit 5 of Elsinore Area Plan; 2,320 acres), Sedco Hills (Proposed Linkage 8; 5,470 acres), Hogbacks (Proposed Core 2; 5,050 acres), Lake Skinner/Diamond Valley Lake (Existing Core C plus Proposed Extension of Core 5, 6, 7; 29,060 acres, Vail Lake/Wilson Valley/Aguanga (Proposed Core 7; 50,000 acres), Tule Valley, (Proposed Core 6; 4,290 acres), Lakeview Mountains (Proposed Noncontiguous Habitat Block 5; 7,150 acres), Lake Perris (Existing Core H; 17,470 acres), Badlands (Proposed Core 3; 24,920 acres), and Box Springs Mountains (Existing Noncontiguous Habitat Block A plus Proposed Constrained Linkage 8; 2,920 acres). The total acreage of Core Areas within Criteria Area and Public/Quasi-Public Lands is 173,590 acres. Some additional locations of Bell's sage sparrows will be conserved within the Sycamore Canyon Regional Park, Steele Peak, North Peak Conservation Bank, Motte-Rimrock Reserve, Santa Rosa Plateau Nature Reserve, and Kabian Park. Although only one location is recorded, the MSHCP Conservation Area within the Gavilan Hills provides potential habitat for Bell's sage sparrow.
Conservation also will be provided for the habitat linkages between Core Areas and areas important for dispersal including the Jurupa Mountains, which is also conserved as a Core Area, Reche Canyon, and San Timoteo Creek areas. Other linkages that may be important for this species and that are within Criteria Area and Public/Quasi-Public Lands include the Gavilan Hills as discussed above, Temecula Creek, a Proposed Linkage to Cactus Valley, Tucalota Valley linkage between Lake Skinner/Diamond Valley Lake area and Vail Lake/Wilson Valley/Aguanga area, Tule Creek, Tenaja Corridor, and a linkage between the Santa Rosa Plateau Nature Reserve and the Santa Margarita Ecological Reserve.
MSHCP Conservation Area Configuration Issues
Several large blocks of habitat supporting the Bell's sage sparrow will be conserved as Criteria Area and Public/Quasi-Public designations including the Core Areas for the species in the Jurupa Mountains (Proposed Noncontiguous Habitat Block 2; 1,230 acres), Lake Mathews-Estelle Mountain (Existing Core C plus Proposed Extension of Existing Core 2; 23,710 acres), Wasson Canyon (2,320 acres), Sedco Hills (Proposed Linkage 8; 5,470 acres), Hogbacks (Proposed Core 2; 5,050 acres), Lake Skinner/Diamond Valley Lake (Existing Core C plus Proposed Extended Core 5, 6, 7; 29,060 acres), Vail Lake/Wilson Valley/Aguanga (Proposed Core 7; 50,000 acres), Tule Valley, (Proposed Core 6; 4,290 acres), Lakeview Mountains (Proposed Noncontiguous Habitat Block 5; 7,150 acres), Lake Perris (Existing Core H; 17,470 acres), Badlands (Proposed Core 3; 24,920 acres), and Box Springs Mountains (Existing Noncontiguous Habitat Block A plus Proposed Constrained Linkage 8; 2,920 acres). By conserving these large blocks of habitats, the edge effects of MSHCP Conservation Areas are reduced which may reduce the effects of edge responsive species such as the brown-headed cowbird, invasion of introduced grasses, and human and urban mesopredator intrusion. Some additional locations of the Bell's sage sparrows will be conserved within the MSHCP Conservation Area outside of the Core Areas including the Sycamore Canyon Regional Park, Gavilan Hills, Steele Peak, North Peak Conservation Bank, Motte-Rimrock Reserve, Kabian Park, and Cleveland National Forest (a likely but not confirmed location).
Areas that are important for preservation for dispersal purposes between the Plan Area and other areas, but that may or may not contain large numbers of Bell's sage sparrows, include the Jurupa Mountains for connectivity to San Bernardino County which is also a Core Area for this species, Chino Hills and Cleveland National Forest for connectivity to Orange County, and the Santa Margarita Ecological Reserve and eastern Temecula Creek for connectivity to San Diego County.
Similar to the California gnatcatcher, the Bell's sage sparrow, as a year-round resident, may not be as adept at dispersing as some of the long distance migrant bird species. Unfortunately, no data is available specific to the Bell's sage sparrow, although the sage sparrow has been documented to be sensitive to fragmentation and edge effects (see below). It is assumed, based on the natural history of this species that the MSHCP Conservation Area will provide habitat linkages between the preserved Core Areas. The large block of habitat within the core population area at Lake Mathews-Estelle Mountain Reserve is connected to the Wasson Canyon population along Temescal Wash and the hillsides east of the wash with a wide linkage at a 2,000 foot minimum width. These Core Areas also are connected by the Proposed Linkage at the Gavilan Hills. Connections to the eastern foothills of the Santa Ana Mountains are located at Indian Canyon, and Horsethief Canyon. The Wasson Canyon population is connected to the Hogbacks population along the Sedco Hills Core Area, and then to the Lake Skinner population via the AD161 mitigation area and conservation of other small drainages including Warm Springs, Ken & Barkley Canyon and Tucalota Creek. The Lake Skinner population is linked to the Vail Lake/Wilson Valley/Aguanga area by preservation within the entire area in Wilson Valley as well as the eastern reach of Tucalota Creek. The Cactus Valley area is a large block of habitat connecting the Lake Skinner/Diamond Valley Lake area east to the San Bernardino National Forest, along Bautista Creek and within the large block of habitat within the Badlands. The block of habitat within the Lake Perris Core Area is connected to the Badlands along the San Jacinto River and Lamb Canyon. The Core Area in the Lakeview Mountains is somewhat isolated from other MSHCP Conservation Area areas due to existing development, however a narrow connection is provided between the north edge of the Lakeview Mountains and the San Jacinto River. The Box Springs Mountains area is connected by Reche Canyon to the Badlands.
MSHCP Conservation Area design for the Bell's sage sparrow will take into account that large scale fires damages habitat for a relatively long length of time and large areas are necessary to provide refugia for birds and to supply dispersing individuals to a recovered area. In contradiction to this, and a complicating factor, is that fire may also assist with providing additional suitable habitat for the Bell's sage sparrow. Long term fire suppression in California has allowed some of the shrub communities to reach tall, thick shrublands reducing the availability of suitable habitat. Fire management will be an important factor in addressing the conservation of this species.
Duplicate linkages also provide for the temporary loss of function of the coastal sage scrub or chaparral habitat in the event of a fire. A duplicity of habitat linkages composed of sage scrub and other undeveloped habitats which may be composed of native as well as non-native habitats may provide for dispersal. Several duplicate linkages are preserved in the MSHCP Plan Area including linkages along the Santa Ana Mountains foothills with the Interstate 15 corridor and between AD161 and the Hogbacks and between the Lake Skinner/Diamond Valley Lake area and other areas to the east.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 245,750 acres of suitable Conserved Habitat and 12 of 14 Core Areas within large blocks of habitat in the MSHCP Conservation Area. In addition, 34 recent and high precision locations will be inside the Criteria Area or Public/Quasi-Public Lands, all of which are recorded for the suitable habitat of Bell's sage sparrow. Conservation also will be provided for the habitat linkages between Core Areas and areas important for dispersal including the Jurupa Mountains, which is also conserved as a Core Area, Reche Canyon, and San Timoteo Creek areas as well as other linkages as described above. The current population size of the Bell's sage sparrow is unknown. However the habitat requirements of the species and locations that constitute key populations are well documented.
INCIDENTAL TAKE
The Incidental Take of the Bell's sage sparrow is difficult to quantify due to our limited knowledge of its distribution and abundance within the Plan Area. The maximum level of Incidental Take of Bell's sage sparrow can be anticipated by the loss of the number of acres of habitat that will become unsuitable for this species. About 177,440 acres of potential habitat for the Bell's sage sparrow will be outside the Criteria Area and Public/Quasi-Public designations, or about 42 percent of the total potential habitat and individuals within these areas are subject to Incidental Take consistent with the Plan. Of this, approximately 73,180 acres (17 percent) of potential habitat are located within Rural/Mountainous designation areas, which may provide some habitat value, but will not be managed for the benefit of covered species and cannot be relied upon as conserved habitat for the Bell's sage sparrow. These areas include the Santa Rosa Plateau, Santa Rosa Hills, and a portion of the Badlands.
Core areas not conserved within Criteria Area and Public/Quasi-Public designations include the Santa Rosa Plateau and Santa Rosa Hills. A total of 64 recent and high precision point locations of the Bell's sage sparrow will be outside the Criteria Area and Public/Quasi-Public designations. Of these 64 point locations, 18 (18 percent) will be in the Rural/Mountainous zone. Of the 46 (47 percent) points located outside the MSHCP Conservation Area, 26 are mapped in existing residential/urban/exotic areas.
SPECIES ACCOUNT
Data Characterization
The UCR location database contains approximately 352 location records for the Bell's sage sparrow dated from 1887 to 1999. Due to its overlap in habitat with the gnatcatcher, the Bell's sage sparrow has probably been well surveyed within sage scrub habitat. In areas where there is no requirement for surveys for the gnatcatcher, the sage sparrow is likely under represented and the documentation of presence in outlying areas probably has not been accomplished. Approximately 264 of the records are relatively recent (within the past 10 years) and approximately 98 of these records are precise. Approximately 26 of these recent and precise records are located within residential or developed habitats and may no longer be extant, the rest are located within sage scrub, chaparral or other undeveloped habitats and may represent existing locations.
The sage sparrow has a moderate amount of literature available for it. It has been well studied with the suite of species located within the shrub-steppe region and has general natural history information well summarized within the ornithological literature. Although, the subspecies and information for the Plan Area have a relatively little amount of literature available, the species as a whole has been well documented for its distribution and biology.
Habitat and Habitat Associations
The sage sparrow prefers semi-open habitats with evenly spaced shrubs 1 to 2 meters high (Martin and Carlson 1998). Vertical structure, habitat patchiness, and vegetation density may be more important in habitat selection by the sage sparrow than the specific shrub species, but this sparrow is closely associated with sagebrush throughout most of its range (Wiens and Rotenberry 1981). The species is often missing from what appears to be suitable habitat, so other unknown habitat characteristics may be important (Martin and Carlson 1998).
Bell's sage sparrow is an uncommon to fairly common but localized resident breeder in dry chaparral and coastal sage scrub along the coastal lowlands, inland valleys, and in the lower foothills of local mountains. In transmontane California, it occupies sagebrush, alkali desert scrub, desert scrub, and similar habitats. In cismontane California, it frequents chaparral dominated by chamise, and coastal scrub dominated by sage. Other coastal scrub plant species associated with Bell's sage sparrow include Artemisia, Purshia, and Atriplex as well as mixed brush and cactus patches in arid washes (Grinnell and Miller, 1944). The preference for chamise chaparral appears to occur only in the more northern parts of its range. High overgrown chaparral stands generally have fewer sage sparrows than shorter shrubs recovering from recent fires (Martin and Carlson 1998). Bell's sage sparrow is also found in big sagebrush at higher elevations in southern mountains (Martin and Carlson 1998).
Bell's sage sparrow seeks cover in fairly dense stands in chaparral and scrub habitats in the breeding season, and they forage on the ground beneath and between shrubs. The species uses similar habitat structure in the winter, however the habitat may be in more arid, open shrub habitats (Zeiner, et al. 1990).
Biogeography
The sage sparrow occurs in western North America from the interior west-central Washington, within the eastern portion of Idaho to western Wyoming, through Nevada, Utah, Colorado south to New Mexico, Arizona and into California. The subspecies Bell's sage sparrow, A. belli belli, occurs as a nonmigratory resident on the coastal ranges of California, on the western slope of the central Sierra Nevada mountains, and into northwestern Baja California (Bent, 1968). Generally it is found throughout the year in southern California and Baja areas where the winter range overlaps with the breeding range (Martin and Carlson, 1998).
Zeiner, et al. (1990) characterized the distribution, abundance and seasonality of the Bell's sage sparrow as follows. It is a common to uncommon resident and summer visitor. In summer, it is uncommon to common east of the Cascade Range and Sierra Nevada, in foothills bounding the Central Valley, and in the Transverse, Peninsular, and coastal ranges from Trinity Co. south to the Mexican border. It is not migratory in many areas, but mostly withdraws from higher elevations and the northern Great Basin in winter and moves to southern deserts. It is most common from the western edge of Owens Valley, Inyo County, south through southern Sierra Nevada and the western edge of Mojave Desert to desert slopes of the Transverse Ranges. On coastal slopes, it is mostly absent north of Sonoma County, and uncommon and local to the south. It occurs only locally at montane elevations, mostly in southern California. The resident race, A. b. clementeae, on San Clemente Island, is classified as a Federally listed threatened species (Grinnell and Miller 1944, McCaskie, et al. 1979, Garrett and Dunn 1981).
Known Populations Within Western Riverside County
The Bell's sage sparrow has a wide but sparse and patchy distribution in western Riverside County. Bell's sage sparrow may occur in extant stands of dry chaparral and coastal sage scrub habitat nearly throughout the Plan Area within the Riverside lowlands, San Jacinto Foothills, Santa Ana Mountains and Desert Transition Bioregions. Although difficult to assign Core Areas to the broad but sparse scatter of database locations some trends of clusters of locations appear to include the areas in the vicinity of Jurupa Mountains, Lake Mathews-Estelle Mountain, Wasson Canyon, Santa Rosa Plateau, Sedco Hills, Hogbacks, Lake Skinner/Diamond Valley Lake, Vail Lake/Wilson Valley/Aguanga, Tule Valley, Santa Rosa Hills, Lakeview Mountains, Lake Perris, Badlands, and Box Springs Mountains (B. Carlson 1998 pers. comm.). Although these areas are considered Core Areas, none of the areas consists of very high or very dense populations except for the Wasson Canyon and Lake Skinner/Diamond Valley Lake areas.
Biology
Genetics: The sage sparrow varies in morphometrics, plumage coloration, and habitat selection in correlation with features that roughly agree with observed genetic and biochemical variation. Within the three subspecies, belli, canescens, and nevadensis, the average percentage of nucleotide difference is 0.1 percent within populations and 0.4 percent between populations within the same subspecies, and 0.6 percent between subspecies (Johnson and Cicero 1991).
Diet and Foraging: Bell's sage sparrows predominantly forage on the ground, mostly by gleaning from the ground and low foliage of shrubs; it rarely catches insects on the wing (Zeiner, et al. 1990). The sage sparrow is categorized as a ground foraging omnivore during the breeding season and a ground gleaning granivore during the nonbreeding period (Martin and Carlson 1998). It feeds mostly on insects, spiders, and seeds while breeding, switching to grasshoppers in the late breeding season (Rotenberry 1980), and mostly on seeds in winter; it also takes green foliage. Apparently, the species drinks regularly (Bent 1968, Smyth and Coulombe 1971). Captives could not survive exclusively on seeds unless supplemented with succulent foods. When water was available, captives drank an average of 49 percent (range 12-99 percent) of body weight daily. It may meet a portion of its water needs from invertebrate foods (Moldenhauer and Wiens 1970).
Daily Activity: A study in Oregon revealed the following breakdown of a sage sparrow's day: 51 percent singing, 35 percent foraging, 12 percent inactivity, 4 percent locomotion and 3 percent aggression (Martin and Carlson 1998). The Bell's sage sparrow exhibits year-long, diurnal activity (Zeiner et al. 1990).
Reproduction: Bell's sage sparrow usually nests in sagebrush or chaparral, and may have two broods per nesting season (Ehrlich, et al. 1988). They prefer to nest in an intermediate sized shrub, 50 to 70 centimeters tall, which may represent a compromise between shrubs that provide favorable foraging sites, avenues of movement, and sufficient cover Martin and Carlson 1998). The subspecies uses a very diverse selection of shrubs including brittlebush (Encelia farinosa), black sage (Salvia mellifera), California buckwheat (Eriogonum fasciculatum), California sagebrush (Artemisia californica), bush mallow (Malocothamnus fasciculatum), chamise (Adenostema fasciculata), white sage (Salvia apiana), valley cholla (Opuntia parryi), ceanothus (Ceanothus sp.), willow (Salix sp.) and bunchgrass species (Martin and Carlson 1998). Individuals remain monogamously pair bonded throughout the year, although partners may change after the breeding season (Martin and Carlson 1998). The nest is a cup of dry twigs and herb stems; it is lined with shreds of bark and grass and contains an inner lining of finer bark fiber, grass, fur, hairs, wool tufts, feathers (Harrison 1978). The nest is located on the ground beneath a shrub; or in a shrub usually 0.15 to 0.45 meters (6-18 inches) above ground, but up to 1 meter (39 inches) in height. It breeds from late March to mid-August with a peak in May and June. The clutch size is 3-5 eggs, usually 3 or 4 eggs. Incubation is typically 13-16 days, and the altricial young fledge in 9-11 days (Harrison 1978, Ehrlich, et al. 1988, Reynolds 1981).
Survival: Sage sparrow populations exhibit substantial yearly fluctuations in population size from unknown causes (30-90 individuals/0.4m2) (Rotenberry 1980, Wiens, et al. 1986, Rotenberry and Wiens 1991). Variations in clutch size have been most strongly correlated with predation; in some cases, predation was by snakes, in other instances by Townsend's ground squirrels (Rotenberry and Wiens 1989).
Dispersal: Young Bell's sage sparrow have been recorded 800 to 900 meters from the nest site by the following spring. Ten hatch-year individuals banded during the breeding season moved 75 to 600 meters by the following spring (Martin and Carlson 1998).
Socio-Spatial Behavior: Male sage sparrows show a strong site tenacity to the breeding territory, even if the habitat is greatly modified (Ehrlich, et al. 1988). In Oregon, Gashwiler (1977) recorded 24-33 pairs per 40 hectares (100 acres). In Nevada, Gustafson (1975) recorded 30 males per 40 hectares (100 acres). Weston and Johnston (1980) reported a density varying from 27-85 individuals per 40 hectares (100 acres) in sagebrush habitat in Mono County. Territory size of the species is highly variable (0.9 to 8.1 acres) depending on local environmental conditions (Reynolds 1981; Rich 1980; Wiens, et al. 1986). For A. belli, the territories in San Diego and Riverside counties varied from 0.75 to 5.7 hectares (Lovio 1993).
Community Relationships: In Nevada, Bond (1940) observed predation by great horned owls. The Bell's sage sparrow is a rare host to cowbird parasitism (Terres 1980).
Threats to Species
Long-term fire suppression alters the pattern of natural plant succession and allows communities to reach tall, thick shrublands, probably reducing the availability of sage sparrow habitat for breeding (Martin and Carlson 1998).
Increasing fire frequency in some areas results in the invasion of exotic weeds. With increased fire frequency, native plants are killed and seed reservoirs of grasses and shrubs are depleted and replaced with exotic annuals (Martin and Carlson 1998).
Loss of coastal sage scrub habitat, which includes foraging, roosting and nesting areas, to development activities, fire, and agriculture appear to the primary threats to the Bell's sage sparrow in western Riverside County. Local populations in some areas of southern California have been extirpated as a result of urbanization and agricultural conversion (Barbara Carlson 1998 pers. comm.).
Threats from brood parasitism and predation have not been quantified (Martin and Carlson 1998).
Special Biological Considerations
Generally associated with dense stands of chaparral or coastal sage scrub, Bell's sage sparrow is one of the first bird species to return after fires in these preferred habitat areas (B. Carlson 1998 pers. comm.). Sage sparrow populations exhibit substantial yearly fluctuations in population sizes, the cause of which is unknown (30-90 individuals/0.4m2) (Rotenberry 1980, Wiens, et al. 1986, Rotenberry and Wiens 1991). The species also shows differences in their behavior from year to year and from habitat area to habitat area (Wiens et al. 1990).
The territory size of sage sparrows appears to be positively related to coverage of spinescent shrub species and to an index of vegetational horizontal heterogeneity or patchiness, while varying inversely with total vegetation coverage and its horizontal variation and with coverage of grass and sagebrush. Thus, over this range of sites, the sage sparrow territories generally were smaller in areas with more grass and sagebrush and larger in the more heterogeneous areas dominated by spinescent shrubs (Wiens et al. 1985). Territories rapidly expand in size at low densities, with no apparent upper limit. At intermediate to high densities, however, territory size hardly changes with increasing density, suggesting that a minimal acceptable size of territory has been reached and that all usable areas, including suboptimal habitat areas have been occupied (Wiens et al. 1985).
Protective fencing in the Mojave Desert increased abundance and nesting activity of sage sparrows (Brooks 1999). Bolger, et al. (1997) studied the 20-most common bird species within a 260 km2 area of coastal San Diego County in relation to edge/fragmentation sensitivity. Bell's sage sparrow was found to be one of four species whose abundance is most reduced by presence of edges/ fragmentation.
Because of the dense habitat and general tendency of this subspecies to stay below the plant canopy and run behind and beneath bushes, it is more difficult to detect than other subspecies (Bent 1968). Population size estimates may be inaccurate owing to the secretive habits of the species. It moves under cover rapidly when approached and incubating birds rarely leave the nest. However, spring counts to assess population numbers are enhanced by the frequent seasonal vocalizations.
The sage sparrow shows an approximate one year time lag in response to habitat changes. This may be due to the site tenacity of the breeding individuals. Such time lags complicate the attempts to formulate management policies on the basis of short-term before and after surveys. It may be necessary to conduct longer periods of post-treatment studies in order to assess true changes in population sizes (Wiens and Rotenberry 1985). Additionally, territory size did not increase significantly over the short term in areas where vegetation was removed and in fact, territory fidelity or tenacity may be a factor for the first 12 years after vegetation removal (Wiens, et al. 1985). In addition, if insular patches of vegetation are left within territories, sage sparrows may adjust to removal without significant density changes. Where individuals are less abundant, they appear to increase territory size with no apparent upper limit, but do not completely saturate the available habitat (Wiens and Rotenberry 1985).
Fragmentation of shrubland habitats has the potential to affect significantly, the conservation of shrub-obligate species because of the potential permanence of the disturbance (Knick and Rotenberry 1995). Disturbance of shrub habitats in the shrubsteppe regions has the potential to allow invasion of exotic species, including grasses, and increase the fire frequency which then changes the dominance of the shrub areas (Knick and Rotenberry 1995). For the Bell's sage sparrow, the total shrub cover and abundance of shrub species (predominantly sagebrush) are important habitat characteristics. Additionally, the importance of landscape characteristics for the Bell's sage sparrow, especially those relating to fragmentation, have been implicated. The Bell's sage sparrow is more likely to remain in an area that has high shrub cover, low disturbance, combined with large patch size and high within-site spatial similarity. The scale at which species presence is influenced has not been quantified but has been determined to be much larger than the size of an individual's home range (Knick and Rotenberry 1995).
LITERATURE CITED
Bent, A.C. 1968. Life histories of North American cardinals, grosbeaks, buntings, towhees, finches, sparrows, and allies. 3 Parts. Edited by O.L. Austin Fr. U.S. Natl.Mus.bull. 237. 1,889 pp.
Bolger, D. T., T. A. Scott and J. T. Rotenberry. 1997. Breeding bird abundance in an urbanizing landscape in coastal Southern California. Conservation Biology 11:406-421.
Bond, R. M. 1940. Food habits of horned owls in the Pahranagat Valley, Nevada. Condor 42:164-165.
Brooks, Matthew. 1999. Effects of protective fencing on birds, lizards, and black-tailed hares in the Western Mojave Desert. Environmental Management 23: 387-400.
Carlson, B. 1998. Pers. Comm.
Ehrlich, R. R., D. S. Dobkin, and D. Wheye. 1988. The Birder's Handbook: A field guide to the natural History of North American Birds. Simon and Schuster, New York.
Garrett, K., and J. Dunn. 1981. Birds of southern California. Los Angeles Audubon Soc. 408pp.
Grinnell, J. and A.H. Miller. 1944. The distribution of the birds of California. Pacific Coast Avifauna 27.
Gashwiler, J. S. 1977. Bird populations in four vegetational types in central Oregon. U.S. Dep. Inter. Fish and Wildl. Serv., Portland OR. Special Tech. Rep. No. 205. 20pp.
Gustafson, J. R. 1975. A sage sparrow egg in a black-throated sparrow nest. Auk 92:805- 806.
Knick, S. T. And J. T. Rotenberry.1995. Landscape characteristics of fragmented shrubsteppe habitats and breeding passerine birds. Conservation Biology 9:1059- 1071.
Harrison, C. 1978. A field guide to the nests, eggs and nestlings of North American birds. W. Collins Sons and Co., Cleveland, OH. 416pp.
Johnson, N. K., and C. Cicero. 1991. Mitochondrian DNA sequence variability in two species of sparrows of the genus Amphispiza. Proc. Inter. Congr. Ornithol. 20: 600-610.
Lovio, J. C. 1993. Diegan coastal sage scrub. I. Breeding bird census. J. Field Ornithol. 64: 95-96.
Martin, John W. and Barbara A. Carlson. 1998. Sage sparrow (Amphispiza belli) In The Birds of North America, No. 326 (A. Poole and F. Gill, eds.) The Birds of North America, Inc., Philadelphia, PA.
McCaskie, G., P. De Benedictis, R. Erickson, and J. Morlan. 1979. Birds of northern California, an annotated field list. 2nd ed. Golden Gate Audubon Soc., Berkeley. 84pp.
Moldenhauer, R. R., and J. A. Wiens. 1970. The water economy of the sage sparrow, Amphispiza belli nevadensis. Condor 72:265-275.
Reynolds, T.D. 1981. Nesting of the sage thrasher, sage sparrow, and Brewer's sparrow in southeastern Idaho. Condor 83: 61-64.
Rich, T. 1980. Territorial behavior of the sage sparrow: spatial and random aspects. Wilson Bulletin 92: 425-438.
Rotenberry, J. T. 1980. Dietary relationships among shrub-steppe passerine birds: competition or opportunism in a variable environment? Ecol. Monogr. 50: 93-110.
Rotenberry, J. T. and J. A. Wiens. 1989. Reproductive biology of shrubsteppe passerine birds: Geographical and temporal variation in clutch size, brood size and fledging success. Condor 91:1-14.
Rotenberry, J.T., and J.A. Wiens. 1991. Weather and reproductive variation in shrub-steppe sparrows: a hierarchical analysis. Ecology 72: 1325-1335.
Smyth, M., and H. M. Coulombe. 1971. Notes on the use of desert springs by birds in California. Condor 73:240-243.
Terres, J. K. 1980. The Audubon Society Encyclopedia of North American Birds. Alfred A. Knopf, New York, New York. 1109pp.
Weston, H. G., Jr., and D. Johnston. 1980. Summer and fall censusing of bird populations in the Bodie/Coleville region. Harvey and Stanley Assoc., Alviso, CA. Rep. To U. S. Dep. Inter. Bur. Land Manage., Bakersfield CA Contract No. CA-01.
Wiens, J.A. and J.T. Rotenberry. 1981. Habitat associations and community structure of birds in shrubsteppe environments. Ecological Monographs 51: 21-41.
Wiens, J.A. and J.T. Rotenberry. 1985. Response of breeding passerine birds to rangeland alteration in a North American shrubsteppe locality. J. Applied Ecology 22: 655-668.
Wiens, J.A. and J.T. Rotenberry, and B. Van Horne. 1985. Territory size variation in shrubsteppe birds. Auk 102: 500-505.
Wiens, J.A., J.T. Rotenberry, and B. Van Horne. 1986. A lesson in the limitations of field experiments: shrub-steppe birds and habitat alteration. Ecology 67: 365-376.
Wiens, J. A., B. Van Horne, and J. T. Rotenberry. 1990. Comparisons of the behavior of sage and Brewer's sparrows in shrubsteppe habitats. Condor 92: 264-266.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
black-crowned night heron (Nycticorax nycticorax) (Breeding Rookeries)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
black-crowned night heron (Nycticorax nycticorax) (Breeding Rookeries)
Status:
State: None
Federal: None
GROUP DESIGNATION AND RATIONALE
Group 2
The black-crowned night heron is relatively well-distributed throughout the MSHCP Plan Area within its suitable habitat; however, it is not predictably distributed within all suitable areas. It occurs at almost all of the open water bodies where emergent or riparian vegetation is present and many of the playas and riparian drainages that may provide foraging opportunities. There are several Core Areas for this species, including Mystic Lake/San Jacinto Wildlife Area, Prado Basin/Santa Ana River, and Collier Marsh. The breeding locations, which have been documented as active or historic, are located at specific sites that require conservation. Because it is well known for using emergent habitat, riparian areas for breeding, and ponds and other aquatic habitat for foraging, but has specific locations that are used for breeding, it is assumed that this species will respond to a landscape level of management with site-specific requirements (e.g., breeding rookeries).
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 16,560 acres of suitable nesting and foraging habitat for the black-crowned night heron including freshwater marsh, playas and vernal pools, riparian scrub, woodland, and forest, and cismontane alkali marsh.
Objective 2
Include within the MSHCP Conservation Area at least the 3 known and historic breeding locations in the Prado Basin/Santa Ana River (9,670 acres), Mystic Lake/San Jacinto Wildlife Area (Subunit 4 of Reche Canyon/Badlands Area Plan; 2,690 acres), and Collier Marsh areas (Proposed Linkage 2; 160 acres).
Objective 3
A 100-meter buffer will be established around the Core Areas identified in Objective 2 as they are incorporated into the MSHCP Conservation Area.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
The black-crowned night-heron is virtually restricted to more aquatic wetlands for foraging but may use more forested riparian areas for nesting (Garrett and Dunn 1988). Because they will use a relatively wide variety of wetlands for various parts of their life history, a wide range of habitats has been included for this analysis. For the purpose of the conservation analysis, potential habitat for the black-crowned night-heron has been separated into the primary breeding habitat which includes freshwater marsh and riparian scrub, forest, and woodland. The secondary habitat, which is composed only of foraging habitat includes playas and vernal pools and cismontane alkali marsh. Based on these habitats, the Plan Area supports approximately 20,560 acres of potential habitat for the black-crowned night-heron composed of 12,680 acres of primary breeding and foraging habitat and 7,880 acres of secondary foraging habitat. Table 1 shows the conservation of potential habitat for the black-crowned night-heron. Overall, approximately 9,840 acres (78 percent) of potential primary breeding and foraging habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public Lands. Approximately 6,720 acres (86 percent) of secondary foraging habitat will be conserved in Criteria Area or existing Public/Quasi-Public lands.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
BLACK-CROWNED NIGHT-HERON
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| Riverside Lowlands and San Jacinto Foothills Bioregions | |||||||
| Primary Habitat for Breeding and Foraging | |||||||
| Freshwater Marsh | 470 | 170 | 240 | 410 | 0 | 60 | 60 |
| Riparian Scrub, Woodland, Forest | 12,210 | 3,570 | 5,860 | 9,430 | 180 | 2,600 | 2,780 |
| Subtotal Primary Habitat | 12,680 | 3740 (30%) |
6100 (48%) |
9840 (78%) |
180 (1%) |
2660 (21%) |
2840 (22%) |
| Secondary Habitat for Foraging | |||||||
| Playas and Vernal Pools | 7,870 | 3,830 | 2,880 | 6,710 | 0 | 1,160 | 1,160 |
| Cismontane Alkali Marsh | 10 | 10 | 0 | 10 | 0 | 0 | 0 |
| Subtotal Secondary Habitat | 7,880 | 3,840 (49%) |
2,880 (37%) |
6,720 (86%) |
0 (0%) |
1,160 (14%) |
1,160 (14%) |
| TOTAL | 20,560 | 7,580 (37%) |
8,980 (44%) |
16,560 (81%) |
180 (1%) |
3,820 (18%) |
4,000 (19%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
In addition, the Riparian/Riverine Areas and Vernal Pools policy described in Section 6.1.2 of the MSHCP, Volume I, provides for conservation of wetlands, which provide habitat for this species, through avoidance and minimization. Mitigation for impacts to wetlands shall be incorporated in accordance with the "No Net Loss" policy of federal and state wetland regulations. The proposed mitigation shall be directly related to the functions and values of the wetland as related to this species and result in equivalent replacement.
As described below under Data Characterization, 29 of the 69 recent point localities have a high location precision. Of these 29 point localities, 5 will be inside the Criteria Area and 5 will be inside the Public/Quasi-Public Lands. In addition, the one known nesting colony location and the potential or historical nesting locations are within the Criteria Area or Public/Quasi-Public Lands. A total of 17 point localities will be outside of the MSHCP Conservation Area. However, these locations, if within a wetland area, will continue to receive protection by the wetland policy. Conservation of this species can be considered from a landscape perspective because the species has well identified habitat requirements.
In addition, there are definable locations composed of Core Areas for focusing conservation efforts which are included within the MSHCP Conservation Area. These conserved Core Areas include the 3 known and historic breeding locations in the Prado Basin/Santa Ana River (9,670 acres), Mystic Lake/San Jacinto Wildlife Area (Subunit 4 of Reche Canyon/Badlands Area Plan; 2,690 acres), and Collier Marsh areas (Proposed Linkage 2; 160 acres). The Core Area at Prado Basin/Santa Ana River includes the only known nesting colony for the black-crowned night-heron and the Core Area at Mystic Lake/San Jacinto Wildlife Area is an historic or potential breeding location. A total of 12,520 acres of Core Areas are conserved within the MSHCP Conservation Area. Additionally, as part of the reserve assembly, a 100-meter buffer will be established around the Core Areas identified above as they are incorporated into the MSHCP Conservation Area.
MSHCP Conservation Area Configuration Issues
Several large blocks of habitat including potential or historic foraging and nesting areas for the black-crowned night-heron will be conserved as Criteria Area and Public/Quasi-Public Lands including the Prado Basin/Santa Ana River, Lake Skinner, Diamond Valley Lake, Lake Mathews, Mystic Lake, San Jacinto Wildlife Area/Mystic Lake, Lake Perris, Wasson Canyon, Temecula and Murrieta creeks, San Timoteo Creek, Temescal Wash, Lake Elsinore, and Vail Lake. The MSHCP Conservation Area will provide adequate habitat for foraging during nomadic visits to the area and migratory stopovers as well as habitat containing potential nest sites with adequate protection around each nest site and foraging areas during the breeding season. Foraging areas are provided at Vail Lake, Lake Skinner, Diamond Valley Lake, San Jacinto Wildlife Area/Mystic Lake, Lake Perris, Lake Elsinore, Lake Mathews, Prado Basin and Santa Ana River, and a variety of other smaller riparian and wetland areas. Potential and known nest sites are provided in the San Jacinto Wildlife Area/Mystic Lake, Collier Marsh, and Prado Basin and foraging for a potential breeding season is provided in the riparian and marsh areas within and around Collier Marsh, within the Santa Ana River system and along the San Jacinto River near the San Jacinto Wildlife Area and Mystic Lake. These MSHCP Conservation Area locations are interconnected as well, though the ability of this species to move long distances may reduce the importance of these linkages for this species.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 16,560 acres of suitable Conserved Habitat including 9840 acres of primary breeding and foraging habitat and 6,720 acres of secondary foraging habitat. Additionally, the three core known or potential breeding locations, Prado Basin/Santa Ana River, Collier Marsh, and Mystic Lake/San Jacinto Wildlife Area within large blocks of habitat are included in the MSHCP Conservation Area. As these Core Areas are incorporated into the MSHCP Conservation Area, a 100-meter buffer will be established around each Core Areas. The current population size of the black-crowned night-heron is unknown.
INCIDENTAL TAKE
The Incidental Take of the black-crowned night-heron is difficult to quantify at this time owing to our limited knowledge of the precise location and extent of nesting sites and the fact that losses may be masked by fluctuations in abundance and distribution during the life of the permit. However, the level of Take of black-crowned night-heron can be anticipated by the loss of the number of acres of habitat that will be impacted or become unsuitable for this species. About 2,840 acres (22 percent) of potential primary breeding and foraging habitat for the black-crowned night-heron will be outside the Criteria Area and Public/Quasi-Public Lands. Approximately 1,160 acres (14 percent) of potential secondary foraging habitat for the black-crowned night-heron will be outside the Criteria Area and Public/Quasi-Public Lands.
This comprises approximately 19 percent of the total potential habitat. No Take of nesting colonies will occur. The estimate of Incidental Take is consistent with the anticipated land uses and the application of the riparian/riverine area and vernal pool avoidance and land use adjacency policies/guidelines.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The UCR location database includes approximately 79 records for the black-crowned night-heron within the Plan Area dated from 1900 to 2000. A total of approximately 69 records are relatively recent (dated since 1990) and of these recent records, 29 are high precision records that can be accurately placed within the area. The habitat types associated with these recent and high precision data records include riparian, agriculture, alluvial, grassland, alkali playa, open water, sage scrub, and residential. The residential habitat records may reflect records that are either no longer extant or where the location is a small pocket of suitable habitat within or adjacent to a developed area. The upland records or records in habitat that is not suitable may also be records of the species observed in a small pocket of suitable habitat that is adjacent to the upland habitat. Breeding locations have not been recorded specifically within the database but have been documented from other sources as identified below.
Habitat and Habitat Associations
Black-crowned night-herons require marshes, ponds, reservoirs, and estuaries for foraging and also occur along the margins of lacustrine, large riverine, and fresh and saline emergent habitats and, rarely, in kelp beds in marine subtidal habitats (Garrett and Dunn 1981; Gallagher 1997). Its habitat requirements are varied, including all types of wetland areas including swamps, streams, rivers, margins of pools, ponds, lakes, lagoons, tidal mudflats, fresh, brackish, and salt water ecosytems and even using man-made ditches, canals, reservoirs, and wet agricultural fields (Davis 1993). In inland areas, most colones are associated with large wetlands. These wetland areas, if they rely on rainfall, may have varying water levels. Therefore, black-crowned night-herons may fluctuate in their usage of such inland areas (Davis 1993). It nests and roosts in dense-foliaged trees, not always near water, and in dense, fresh or brackish emergent wetlands (Grinnell and Miller 1944). As might be expected of a widely distributed, opportunistic forager, these birds use a broad spectrum of habitat types for nesting, and choose nest sites from ground to 160 feet in height (Palmer 1962). Most colony sites are on islands, in swamps, or over water, suggesting that site selection may be related to predator avoidance. The variety of substrates used for nesting is enormous including oak trees, willow trees, poison ivy, box elder trees, cattails, and areas level with the water surface supported by floating dead vegetation (Davis 1993). It often rests on piers and pilings (Zeiner, et al. 1990).
Biogeography
Black-crowned night-herons breed in the western hemisphere from British Columbia eastward to Nova Scotia southward locally through the Americas to southern South America. The species winters locally from Washington to New England southward throughout the remainder of the breeding range (AOU 1998). The distribution of the species is generally determined by the suitable wetland habitat for feeding. The colonies are locally distributed within this range and they often occur on islands (Davis 1993).
Hunting, disturbance at breeding colonies, drainage of wetlands, and land development for homes and recreation have caused declines in heron numbers (Gross 1923; Davis 1993). DDT and other pesticides are thought to have caused local reproductive failure and population declines but convincing documentation is lacking and sparse census data from the early 20th century makes trend analysis difficult (Davis 1993).
Zeiner, et al. (1990) summarize the distribution, abundance, and seasonality of the black-crowned night-heron within California as follows. The black-crowned night-heron is a fairly common, year-long resident in lowlands and foothills throughout most of California, including the Salton Sea and Colorado River areas, and very common locally in large nesting colonies. It is a common nesting species on the northeastern plateau of California from April to August. It is uncommon in the northwestern part of the state, and rare in northeastern California in midwinter. It is an uncommon transient and rare species in winter in the southern deserts, and rare on the Channel Islands. It is seldom seen in the mountains, but formerly nested at Big Bear Lake in San Bernardino Mts. (Cogswell 1977, McCaskie, et al. 1979, Garrett and Dunn 1981). In southern California, the species generally occurs locally throughout as a year round resident except for mountainous and desert areas (Garrett and Dunn 1981). Rookeries are scarce within southern California. It is a local migrator, dispersing widely from breeding colonies after nesting (Gill and Mewaldt 1979). Much of the breeding population from northwestern and northeastern California probably moves southward and is absent from those areas in midwinter.
Known Populations Within Western Riverside County
The black-crowned night-heron may be found throughout the Plan Area in appropriate habitat within Riverside lowland and San Jacinto Foothills Bioregions. The only known recently active rookery in western Riverside County is in the Prado Basin (Patten 1998, pers. comm.) . However, there was no direct evidence of nesting in the Prado Basin in recent years (Pike, 2001, pers. comm.). Additional potential locations include Collier Marsh, Mystic Lake/San Jacinto Wildlife Area (the species formerly bred at this locale [Garrett and Dunn 1981]), Lake Mathews, Vail Lake, Lake Perris, and Lake Skinner.
Other geographic locations recorded within the U.C. Riverside database include: Santa Ana River, Temescal Wash, Cajalco Creek, Woodcrest, Moreno Valley, Lake Perris, San Timoteo Creek, San Jacinto River, Winchester, Canyon Lake, Temecula Creek, and Lake Skinner.
Biology
Genetics: Sheldon's (1987) DNA-DNA hybridization work on the phylogeny of herons generally supports a linear arrangement of herons beginning with day and night herons and ending with tiger herons and bitterns, but suggests that no great genetic distinction exists between the day and night herons. It is concluded that the yellow-crowned and black-crowned night-herons are as divergent genetically from each other as either is from most day herons.
Diet and Foraging: The black-crowned night-heron feeds along the margins of lacustrine, large riverine, and fresh and saline emergent habitats and rarely on kelp beds in marine subtidal habitats. It prefers shallow, weedy pond margins, creeks, and marshes (Davis 1993). One study listed the following food items found in regurgitated samples: annelids, insects, crustaceans, amphibians and fishes, with fishes being dominant (Sodhi 1992). Other investigators have described the diet as: a highly variable diet consisting of fishes, crustaceans, aquatic insects and other invertebrates, amphibians, reptiles, small mammals, and rarely young birds (Palmer 1962, Wolford and Boag 1971b). Collins (1970) and Hunter and Morris (1976) reported observing the species feeding on young terns. It usually hunts in shallow water, waiting motionlessly or, less commonly, stalking its prey slowly (Kushlan 1976a). Sometimes it vibrates its bill to lure or flush prey, and it may alight briefly on deep water to make a strike.
Daily Activity: The black-crowned night-heron feeds mostly nocturnally and crepuscularly and sometimes also feeds diurnally (Zeiner, et al. 1990; Terres 1980). It generally feeds throughout the night, avoiding competition with day herons which use the same habitat (Kushlan 1973).
Reproduction: Nests of the black-crowned night-heron are located in dense-foliaged trees, dense, fresh or brackish emergent wetlands, or dense shrubbery or vine tangles, usually near aquatic or emergent feeding areas. The nests are built of twigs and/or marsh plants (Zeiner, et al. 1990). The nest is usually a platform of sticks of whatever trees or vegetation is available. As an example, they may use box elder, cedar, oak, pine, bayberry, plum, and cattails (Davis 1993). Some nests are sturdy, others are flimsy and the eggs are visible from below. Nest-sites are usually near aquatic or emergent feeding areas, but the non-breeding-season roosts may be farther away. Nests can be near tree trunks or distal forks of branches, in the open or deep in the foliage (Davis 1993). Beaver et al. (1980) gives the average nest heights and standard deviations for colonies as 2.6 meters + 0.93.
The species breeds mainly February to July, but also April to August in northeastern California (Cogswell 1977). It is a monogamous, colonial nester. The clutch size is 3-4 eggs, sometimes 5 eggs. The mean clutch size for 684 nests in a South San Francisco Bay colony (Bair Island) in May 1971, was 2.9 eggs (Gill 1977). Incubation is reportedly 24-26 days. The semi-altricial, downy young are tended by both parents. They fly first at six weeks, but are not independent until some time later. A few breed at 1 year, but most do not breed until 2-3 years of age (Palmer 1962, Harrison 1978).
Survival: The nesting success of the black-crowned night-heronis mainly affected by avian predation for a current population in Oregon and Washington (Blus, et al. 1997). Survival rates measured for chicks in coastal Virginia were between 0.90 and 1.00 during the first two weeks of life and between 0.25 and 0.60 during the next 40 to 55 days when birds have left their birth colony (Erwin, et al. 1996). There are banding recoveries for birds aged 15 years to 21 years (Davis 1993).
Dispersal: Many year-old black-crowned night-herons return to the vicinity of their natal colony, but many are widely dispersed and may end up thousands of miles from the natal area. The juvenile birds disperse widely in all directions after nesting but make relatively restricted movements thereafter (Davis 1993, Erwin et al. 1996).
Socio-Spatial Behavior: The black-crowned night-heron occurs in large nesting colonies. Individuals can be relatively social during their foraging activity. In North Carolina they may forage up to 8 kilometers (5 miles) from the nesting area (Custer and Osborn 1978). The breeding territory, used for courtship, copulation, and nesting, is large initially, but shrinks after pair-formation to a few feet around the nest (Palmer 1962). Sometimes the species defends roosting and feeding territories (Palmer 1962).
Community Relationships: Corvidae and other predators eat the eggs of black-crowned night-herons (Zeiner, et al. 1990). The black-crowned night-heron is gregarious at all seasons. It may nest in the same tree with most North American day herons and several species of ibises. It occurs in communal roosts in winter. It is usually a solitary forager and often is supplanted or driven off by day herons during the breeding season (Davis 1993).
Threats to Species
Grinnell and Miller (1944) reported that whereas the black-crowned night-heron was formerly abundant within the State of California, it was by then greatly depleted locally. Although habitat destruction and persecution (Gallagher 1997) are implicated in the species' decline, environmental contaminants and disease may also be problematical, as is evidenced by recent, massive die-offs of water-associated species at the Salton Sea (USFWS, 1999, unpublished data).
Human disturbance of nesting colonies in Quebec (simulating a typical scientific nesting study) resulted in nest abandonment, predation of eggs, and reduced late-season nesting (Tremblay and Ellison 1979). Numbers have been reduced from the drainage of marshes and swamps, and cutting of trees, but this species is more adaptable and persistent than most other herons, bitterns, and egrets (Davis 1993).
Special Biological Considerations
The black-crowned night-heron rookery in the Prado Basin apparently is one of few undisturbed colonies in coastal southern California, although nesting was not confirmed for the 2001 breeding season. For instance, several potential breeding records in Orange County came to light during the breeding bird atlas effort there because citizens reported the felling of trees supporting heron nests which then destroyed the colony (Gallagher 1997).
LITERATURE CITED
AOU (American Ornithologists' Union). 1998. Check-List of North American Birds. Seventh Edition. American Ornithologists' Union, Washington, D.C. 829 pp.
Beaver, D. L., R. G. Osborn, and T. W. Custer. 1980. Nest-site and colony characteristics of wading birds in selected Atlantic coast colonies. Wilson Bull. 92: 200-220.
Blus, L. J., B. A. Rattner, M. J. Melancon, and C. J. Henny. 1997. Reproduction of black-crowned night-herons related to predation and contaminants in Oregon and Washington, USA. Colonial Waterbirds 20:185-197.
Cogswell, H. L. 1977. Water birds of California. Univ. California Press, Berkeley. 399pp
Collins, C. T. 1970. The black-crowned night heron as a predator of tern chicks. Auk 87:584-586.
Custer, T. W., and R. G. Osborn. 1978. Feeding habitat use by colonially-breeding herons, egrets, and ibises in North Carolina. Auk 95:733-743.
Davis, W. E. Jr. 1993. Black-crowned night-heron (Nycticorax nycticorax). In The Birds of North America, No. 205 (A. Poole and F. Gill, eds.). The Academy of Natural Sciences, Philadelphia, and The American Ornithologists' Union, Washington, D.C.
Erwin, R. M., J. G. Haig, D. B. Stotts and J. S. Hatfield. 1996. Reproductive success, growth and survival of black-crowned night-heron (Nycticorax nycticorax) and snowy egret (Egretta thula) chicks in coastal Virginia. Auk 113:119-130.
Erwin, R.M., J.G. Haig, D.B. Stotts, and J.S. Hatfield. 1996. Dispersal and habitat use by post-fledging juvenile snowy egrets and black-crowned night herons. Wilson Bulletin 108:342-356.
Erwin, R. M., J. S. Hatfield, and W. A. Link. 1991. Social foraging and feeding environment of the black-crowned night-heron in an industrialized estuary. Bird Behaviour 9:94:102.
Gallagher, S. 1997. Breeding Bird Atlas (Orange County). Sea and Sage Audubon Press, Santa Ana, California. 264 pp.
Garrett, K. and J. Dunn. 1981. Birds of Southern California: Status and Distribution. Los Angeles Audubon Society. 407 pp.
Gill, R. E., Jr. 1977. Breeding avifauna of the South San Francisco Bay estuary. West. Birds 8:1-12.
Gill, R. E., Jr., and L. R. Mewaldt. 1979. Dispersal and migratory patterns of San Francisco Bay produced herons, egrets, and terns. North Am. Bird Bander 4:4-13.
Grinnell, J. and A.H. Miller. 1944. The Distribution of the Birds of California. Pacific Coast Avifauna Number 27. Copper Ornithological Club, Berkeley, California. Reprinted by Artemisia Press, Lee Vining, California; April 1986. 617 pp.
Gross, A. O. 1923. The black-crowned night heron of Sandy Neck. Auk 40: 1-30.
Harrison, C. 1978. A field guide to the nests, eggs and nestlings of North American birds. W. Collins Sons and Co., Cleveland, OH. 416pp.
Hunter, R. A., and R. D. Morris. 1976. Nocturnal predation by a black-crowned night heron at a common tern colony. Auk 93:629-632.
Kushlan, J. A. 1973. Black-crowned night-heron diving for prey. Fla. Field Nat. 1: 27-28.
Kushlan, J. A. 1976. Feeding behavior of North American herons. Auk 93:86-94.
Landin, M. C. and R. F. Soots. 1977. Colonial bird use of dredged material islands: a national perspective. Proc. Colon. Waterbird Group 1977: 62-72.
McCaskie, G., P. De Benedictis, R. Erickson, and J. Morlan. 1979. Birds of northern California, an annotated field list. 2nd ed. Golden Gate Audubon Soc., Berkeley. 84pp.
Palmer, R. S., ed. 1962. Handbook of North American birds. Vol. 1. Yale University Press, New Haven, CT. 567pp.
Patten, M. 1998. Riverside County Editor for American Field Notes and Past Secretary, California Bird Records Committee, pers. comm.
Pike, J. 2001. USFWS Volunteer Field Biologist, pers. comm.
Sheldon, F. H. 1987. Phylogeny of herons estimated from DNA-DNA hybridization data. Auk 104: 970108.
Sodhi, N. S. 1992. Food of black-crowned night-heron nestlings. Pavo 23:47-52.
Terres, J. K. 1980. The Audubon Society Encyclopedia of North American birds. A. Knopf, New York. 1100pp.
Tremblay, J., and L. N. Ellison. 1979. Effects of human disturbance on breeding of black- crowned night herons. Auk 96:364-369.
USFWS, 1999, unpublished data.
Wolford, J. W., and D. A. Boag. 1971a. Distribution and biology of black-crowned night herons in Alberta. Can. Field-Nat. 85:13-19.
Wolford, J. W., and D. A. Boag. 1971b. Food habits of black-crowned night herons in southern Alberta. Auk 88:435-437.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
black swift (Cypseloides niger) - breeding
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
black swift (Cypseloides niger) - breeding
Status:
State: Species of Special Concern
Federal: Partners in Flight Watch List; Fish and Wildlife Service Migratory Nongame Birds of Management; San Bernardino National Forest Sensitive
GROUP DESIGNATION AND RATIONALE
Group 1
The black swift has been recorded in very low numbers spread widely over the Plan Area. Almost all of the observations are of migrating individuals except for the vicinity of the known nesting location in the San Jacinto Mountains. It will forage on the wing in every habitat available within the Plan Area. It has very specialized nest site requirements that only occur in one or possibly two locations within the Plan Area both of which are located within the San Bernardino National Forest. For foraging purposes, it can be managed on a landscape level.
The black swift is designated as a Forest Service Sensitive Species. Forest Service Sensitive Species are protected through the implementation of Forest plans and the biological evaluation (BE) process, which considers the potential effects of Forest Service activities on these species.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation area at least 34,020 acres of deciduous woodland and forest and montane coniferous forest within the San Bernardino Mountains and San Jacinto Mountains Bioregions to provide breeding and foraging habitat, including the known nesting location of the black swift at Tahquitz Creek within the San Jacinto Wilderness Area and the potential nesting location at the north fork of the San Jacinto River in the San Jacinto Mountains.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
For the purpose of the conservation analysis, habitats for the black swift include montane coniferous woodland and deciduous woodland and forest habitats of the San Jacinto Mountains and San Bernardino Bioregions that contain mountainous waterfalls and cliffs required for nesting and roosting. One black swift nest site and another potential nest site have been documented within the habitat and the area is likely to contain additional cliffs suitable for nesting and roosting. Based on these habitats, the Plan Area supports approximately 46,290 acres of potential habitat for the black swift. Table 1 shows the conservation and loss of potential habitat for the black swift. Overall, approximately 34,020 acres (73 percent) of potential habitat will be conserved in the Criteria Area or existing Public/Quasi-Public lands.
The one known nest location at the falls on Tahquitz Creek, and a potential nest site on the north fork of the San Jacinto River, will be conserved within Public/Quasi-Public Lands. Other likely nest locations within cliff areas are generally located within The San Jacinto Wilderness Area, which will be conserved.
The MSHCP indicates that the black swift will be conserved at the landscape level. Conserving large blocks of suitable habitat within the area of known occurrences and nest site locations will capture additional localities of the black swift. The U.S. Forest Service will need to manage known and potential nest sites as well as maintain the condition of the waterfalls within the drainages where nesting may occur. Additionally, since waterfalls are also popular recreation sites, the U.S. Forest Service management attention is needed to ensure that black swift nest sites are not disturbed (Stephenson and Calcarone 1999).
TABLE 1
SUMMARY OF HABITAT CONSERVATION
BLACK SWIFT
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| San Jacinto Mountains and San Bernardino Mountains Bioregions | |||||||
| Deciduous Woodlands and Forests | 16,490 | 300 | 13,320 | 13,620 | 850 | 2,020 | 2,870 |
| Montane Coniferous Forest | 29,800 | 20 | 20,380 | 20,400 | 40 | 9,360 | 9,400 |
| TOTAL | 46,290 | 320 (<1%) |
33,700 (73%) |
34,020 (73%) |
890 (2%) |
11,380 (25%) |
12,270 (27%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
MSHCP Conservation Area Configuration Issues
Several large blocks of habitat supporting the known and potential foraging and nesting locations of the black swift will be conserved within the Criteria Area and Public/Quasi-Public lands, including deciduous and coniferous woodland habitat within the San Jacinto Mountains and San Bernardino Mountains Bioregions. Good dispersal and foraging capabilities allow the black swift to use foraging and migration habitat throughout the MSHCP Plan Area. As such, the MSHCP Conservation area will provide adequate foraging and migration areas for this species.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 34,020 acres of suitable Conserved Habitat, including montane coniferous woodland and deciduous woodland and forest habitats of the San Jacinto Mountains and San Bernardino Bioregions. In addition, the one known and one potential nest site will be conserved in the MSHCP Conservation Area. The current population size of the black swift within the Plan Area is unknown.
INCIDENTAL TAKE
The Incidental Take of the black swift is difficult to quantify due to our limited knowledge of its distribution and abundance within the Plan Area. The maximum level of Incidental Take of black swift can be anticipated by the loss of the number of acres of habitat. Approximately 12,270 acres (27 percent) of potential habitat for the black swift will be outside the Criteria Area and Public/Quasi-Public Land designations and individuals within this area will be subject to Incidental Take consistent with the Plan. No known nesting locations will be subject to Take.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The location database for the black swift includes nine records dated from 1897 to 1999. The older records (1959 and earlier) are likely from museum records or skins and all but two of the records are lacking precision to be able to locate the record accurately. Two records, from 1995 and 1999, are of high precision and documented to occur within riparian and oak woodland habitat and likely accurately reflect the low population numbers within the Plan Area. These two records are of foraging individuals and probably were recorded during migration.
Little literature is available for the black swift probably due to its low population size. Most of the available information is relatively old or is very general in nature and descriptive of the natural history of the species. There are no controlled scientific studies that have been conducted and little management information is available. Very little information is available for the Plan Area other than what is available regarding basic distribution information.
Habitat and Habitat Associations
The black swift is observed flying high over western mountains and canyons and thus is not documented as being present very often. If there are suitable nest sites for breeding, the black swift will forage over almost any terrain and habitat (Lack 1956). It nests in moist crevices or caves on sea cliffs above the surf, or on cliffs behind, or adjacent to, waterfalls in deep canyons (Lack 1956). It forages widely over many habitats. It lives where there are rocky cliffs available for its somewhat specialized nest site but has great powers of flight and often ranges far away from the nesting area. It generally requires coastal or mountain cliffs (Terres 1980). Habitats that are used by the black swift in the Sierra Nevada include montane hardwood conifer forest, mixed conifer, Jeffrey pine forest, red fir, lodgepole pine forest, montane riparian habitat, barren habitat, and douglas fir forest (DeSante 1999).
Biogeography
It breeds from southeastern Alaska, British Columbia, western Washington, Montana, south to the Rocky Mountain States, New Mexico, Nevada and to southern California, south to Costa Rica and the West Indies. Its winter range is not precisely known but it includes tropical America. The areas where it occurs in highest abundance are the Pacific Northwest regions and coastal British Columbia (Terres 1980). Black swifts tend to be more common along the west coast states from Mexico north into Canada. Their range extends into Arizona and Colorado.
The black swift breeds very locally in the Sierra Nevada and Cascade Range, the San Gabriel, San Bernardino, and San Jacinto Mountains, and in coastal bluffs and mountains from San Mateo County south probably to San Luis Obispo County. It seems to avoid arid regions, however, such as the Great Basin, southern deserts, and Central Valley. In migration, it is rare and irregular outside the breeding range and does not winter in the state (Grinnell and Miller 1944, Remsen 1978, McCaskie, et al. 1979, McCaskie et al. 1988, Garrett and Dunn 1981). The black swift migrates south for the winter and is mostly absent from October through April. It is noted rarely and irregularly outside the breeding range, mostly west of the Great Basin and southern deserts (Knorr 1961).
Known Populations Within Western Riverside County
The black swift is present within western Riverside County as a breeding bird in the San Bernardino and San Jacinto Mountains (Zeiner, et al. 1990). It is documented as breeding at Tahquitz Creek and probably the north fork of the San Jacinto River in the San Jacinto Mountains (Garrett and Dunn 1981). Although recorded in other parts of the Plan Area, these location records are probably of migrant individuals which occur within the area on an irregular basis. It has been documented in the literature to occur in other parts of the Plan Area as an irregular transient (Garrett and Dunn 1981).
Biology
Genetics: The groupings of the species within each genera of the swift family are based on the stiffening of the rectrices and the presence or absence of spiny tips on the tail feathers (Lack 1956). The black swift is different from other congeners due to its normal tail feathers without spiny tips. All the rest of the congeners have rectrices somewhat stiffened with slightly projecting bare tips. However, with the dark plumage of C. niger and its nesting habits, it is in close relationship with the rest of the Cypseloides (Lack 1956).
Diet and Foraging: The black swift feeds exclusively on flying insects, captured in sustained, long-distance foraging flights, usually high in the air. It often pursues insects in updrafts associated with cliffs or storm fronts (Udvardy 1954). Winged ants comprise 91 percent of the prey items provided to the nestlings (Marin 1999). Other food items include caddis flies, mayflies, crane flies, flesh flies, midges, beetles, termites, aphids, bees, wasps, and spiders (Terres 1980).
Daily Activity: The black swift exhibits diurnal activity, including during migration (Zeiner et al. 1990). Other swifts undergo periods of torpor in cold weather, when flying insects are scarce (Terres 1980), and the black swift may do the same. Apparently the only regular resting or roosting places are on steep, rocky, often moist, cliffs, such as those used for nesting (Bent 1940).
Reproduction: The black swift builds its nest in moist locations, usually associated with water, on a sea cliff above the surf, or on the cliff behind, or adjacent to a waterfall in a deep canyon (Lack 1956; Marin 1997). The nest location must provide complete protection from rain, wind and sunshine and tends to be located on inaccessible cliffs at isolated locations (Michael 1927). The nest is constructed of mud mixed with moss, ferns, seaweed, or other plant materials; it is located in a deep, dark crevice, in a cave, or under an overhang (Bent 1940). It nests in a colony of a few pairs; six nests were observed at a location in Yosemite (Lack 1956; Michael 1927). The nest is usually kept moist by mist from the surf or waterfall (Lack 1956). The breeding season lasts from early June to late August with the peak egg-laying period in mid-June (Lack 1956; Marin 1999). It lays only 1 large egg per year (Harrison 1978; Marin 1997; Knorr 1961). Incubation lasts 24-27 days. The altricial young leave the nest at about 45 days (Hunter and Baldwin 1962), but the nestling period is probably highly variable as in other swifts (Lack 1956). The young can go without food for long periods (Terres 1980).
Survival: No information is available in the literature.
Dispersal: Summer movements of the black swift may be of great distances extending to areas several hundred or even more than a thousand miles from the breeding localities and that distance is easily flown in two or three days. These movements appear to be related to weather conditions and seasonal cyclones (Udvardy 1954).
Socio-Spatial Behavior: The home range of the black swift is very large, but has not been measured (Bent 1940, Grinnell and Miller 1944). Territoriality has not been reported for this species. The territory is presumably limited to the nest site (Zeiner, et al. 1990).
Community Relationships: Nests of the black swift are inaccessible to terrestrial predators and human disturbance, with the exception of rock climbers, who rarely use these wet cliffs (Zeiner, et al. 1990).
Threats to Species
No information is available in the literature. Potential threats to the species may be related to the relatively narrow requirements for the nesting location (see below) and the relatively few situations available within the range of the species that satisfy these requirements.
Conflicts related to nesting black swifts could include rock climbing, spelunking, mining, road construction, hiking, bicycling, horseback trails, water diversions, and housing developments. Probably the greatest disturbance to the black swift nesting habitat is hiking trails to the base or top of waterfalls and any rock or ice climbing. The effect that ice climbing may have on nesting habitat needs research. Rock climbing can remove lichens, mosses and other hydrophilic plants needed in the building of nests, and climbing at waterfalls could disturb incubation, brooding, and foraging of swifts (Colorado Partners in Flight 2000).
Special Biological Considerations
Five ecological features seem to be of importance for the presence of black swifts within an area within their range: the presence of water, high relief as regards the configuration of the terrain, inaccessibility, darkness, and the lack of flyway obstructions (Knorr 1961). The discussion of these ecological requirements is as follows (Knorr 1961). Without exception, water is present at every nesting site, varying in degree from a rushing torrent to a mere trickle, although the former seems to be preferred. There appears to be a requirement that the nesting site have a commanding position above the surrounding terrain so that birds flying out from the nest on a horizontal course find themselves automatically at feeding altitude above the adjacent valley. The requirement that a black swift nest be inaccessible to terrestrial predators appears to be inflexible. No nest has been found which was accessible to anything without wings. It appears that the gloom of the innermost recesses in the rock is preferred to lighter situations and it has been observed that the sun rarely shines on the nest. In conjunction with the requirement of high relief, the air immediately in front of a nesting site must be free of obstructions such as trees or tree branches.
LITERATURE CITED
Bent, A. C. 1940. Life histories of North American cuckoos, goatsuckers, hummingbirds, and their allies. U.S. Natl. Mus. Bull. 176. 506pp.
Colorada Partners in Flight. 2000. Physiographic Region 62:Southern Rocky Mountains.
DeSante, D. 1999. Species Accounts of the Sierra Nevada Bird Conservation Plan. www.prbo.org CPIF/Sierra.
Garrett, K., and J. Dunn. 1981. Birds of southern California. Los Angeles Audubon Soc. 408pp.
Grinnell, J., and A. H. Miller. 1944. The distribution of the birds of California. Pac. Coast Avifauna No. 27. 608pp.
Harrison, C. 1978. A field guide to the nests, eggs and nestlings of North American birds. W. Collins Sons and Co., Cleveland, OH. 416pp.
Hunter, W. F., and P. H. Baldwin. 1962. Nesting of the black swift in Montana. Wilson Bull. 74:409-416.
Knorr, O. A. 1961. The geographical and ecological distribution of the black swift in Colorado. Wilson Bull. 73:155-170.
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burrowing owl (Athene cunicularia hypugaea)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
burrowing owl (Athene cunicularia hypugaea)
Status:
State: Species of Special Concern
Federal: Federal Special Concern species; Partners in Flight Priority Bird Species; Fish and Wildlife Service Species of Management Concern
GROUP DESIGNATION AND RATIONALE
Group 3
The burrowing owl is narrowly distributed at relatively few locations within the Plan Area in suitable habitat. Although the preferred habitat, grassland and some forms of agriculture land, is well distributed, the recent locations of the burrowing owl are clumped in only a few locations. Because this species requires specific soil and micro-habitat conditions, occurs in few locations within a broad habitat category, requires a relatively large home range to support its life history requirements, occurs in relatively low numbers, and is semi-colonial, the burrowing owl will require site-specific considerations and management conditions.
This is a species on the Additional Survey Needs and Procedures (Section 6.3.2) list and surveys for burrowing owl will be conducted as part of the project review process for public and private projects within the burrowing owl survey area where suitable habitat is present (see Burrowing Owl Survey Area Map, Figure 6-4 of the MSHCP, Volume I). Burrowing owls located as a result of survey efforts shall be conserved in accordance with procedures described within Section 6.3.2, MSHCP, Volume 1.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 27,470 acres of suitable primary habitat for the burrowing owl including grasslands.
Objective 2
Include within the MSHCP Conservation Area at least 5 Core Areas and interconnecting linkages. Core areas may include the following: (1) Lake Skinner/Diamond Valley Lake area (Existing Core C plus Proposed Extension of Existing Cores 5, 6, 7; 29,060 acres); (2) playa west of Hemet (Proposed Noncontiguous Habitat Block 7; 1,250 acres); (3) San Jacinto Wildlife Area/Mystic Lake area including Lake Perris area (Existing Core H; 17,470 acres); (4) Lake Mathews (Existing Core C plus Proposed Extension of Existing Cores 2; 23,710 acres); and (5) along the Santa Ana River (9,670 acres). The Core Areas should support a combined total breeding population of approximately 120 burrowing owls with no fewer than five pairs in any one Core area.
Objective 3
Include within the MSHCP Conservation Area at least 22,120 acres of suitable secondary habitat for the burrowing owl including playas and vernal pools, and agriculture outside of the Core Areas identified above. Areas where additional suitable habitat could be conserved include west of the Jurupa Mountains, near Temescal Wash (i.e., vicinity of Alberhill), near Temecula Creek, within the Lakeview Mountains, Banning, the Badlands, Gavilan Hills, and Quail Valley.
Objective 4
Include within the MSHCP Conservation Area the known nesting locations of the burrowing owl at Lake Perris, Mystic Lake/San Jacinto Wildlife area, Lake Skinner area, the area around Diamond Valley Lake, playa west of Hemet, Lakeview Mountains, Lake Mathews/Estelle Mountain Reserve and Sycamore Canyon Regional Park.
Objective 5
Surveys for burrowing owl will be conducted as part of the project review process for public and private projects within the burrowing owl survey area where suitable habitat is present (see Burrowing Owl Survey Area Map, Figure 6-4 of the MSHCP, Volume I). The locations of this species determined as a result of survey efforts shall be conserved in accordance with procedures described within Section 6.3.2, MSHCP, Volume I and the guidance provided below:
Burrowing owl surveys shall be conducted utilizing accepted protocols as follows. If burrowing owls are detected on the project site then the action(s) taken will be as follows:
If the site is within the Criteria Area, then at least 90 percent of the area with long-term conservation value will be included in the MSHCP Conservation Area. Otherwise:
- If the site contains, or is part of an area supporting less than 35 acres of suitable habitat or the survey reveals that the site and the surrounding area supports fewer than 3 pairs of burrowing owls, then the on-site burrowing owls will be passively or actively relocated following accepted protocols.
- If the site (including adjacent areas) supports three or more pairs of burrowing owls, supports greater than 35 acres of suitable habitat and is non-contiguous with MSHCP Conservation Area lands, at least 90 percent of the area with long-term conservation value and burrowing owl pairs will be conserved onsite.
The survey and conservation requirements stated in this objective will be eliminated when it is demonstrated that Objectives 1 – 4 have been met.
Objective 6
Pre-construction presence/absence surveys for burrowing owl within the survey area where suitable habitat is present will be conducted for all Covered Activities through the life of the permit. Surveys will be conducted within 30 days prior to disturbance. Take of active nests will be avoided. Passive relocation (use of one way doors and collapse of burrows) will occur when owls are present outside the nesting season.
Objective 7
Translocation sites for the burrowing owl will be created in the MSHCP Conservation Area for the establishment of new colonies. Translocation sites will be identified, taking into consideration unoccupied habitat areas, presence of burrowing mammals to provide suitable burrow sites, existing colonies and effects to other Covered Species. Reserve Managers will consult with the Wildlife Agencies regarding site selection prior to translocation site development.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
The burrowing owl uses predominantly open land, including grassland, agriculture (e.g., dry-land farming and grazing areas), playa, and sparse coastal sage scrub and desert scrub habitats (Garrett and Dunn 1988). Some breeding burrowing owls are year-round residents and additional individuals from the north may winter throughout the MSHCP Area Plan. For the purpose of the conservation analysis, the primary habitat of the species is considered to include only grassland. The burrowing owl is also known to use some forms of agricultural lands, playa and vernal pool (especially in its grassy condition) and sparsely vegetated scrub habitats. However, these habitat types are considered to be secondary in importance. Due to the overall low occurrence of sparse scrub habitat within the larger habitat category of coastal sage scrub, this habitat type is not included in the analysis. Based on these habitats, the Area Plan supports a total of approximately 109,960 acres of potential primary habitat and approximately 123,520 acres of secondary habitat for the burrowing owl. Table 1 shows the conservation and loss of potential habitat for the burrowing owl. Overall, approximately 27,470 acres (25 percent) of potential primary habitat and 22,120 acres (18 percent) of secondary habitat in the Area Plan will be conserved.
As described below under Data Characterization, 38 of the 82 recent point localities have a high location precision. Of these 38 point localities, 16 will be inside the MSHCP Conservation Area or Public/Quasi-Public Lands. A total of 22 point localities will be outside of the MSHCP Conservation Area.
Five of the six Core Areas will be conserved within Criteria Area and Public/Quasi-Public designations including Lake Skinner/Diamond Valley Lake area (Existing Core C plus Proposed Extension of Existing Cores 5, 6, 7; 29,060 acres); playa west of Hemet (Proposed Noncontiguous Habitat Block 7; 1,250 acres); San Jacinto Wildlife Area/Mystic Lake area including Lake Perris area (Existing Core H; 17,470 acres); Lake Mathews (Existing Core C plus Proposed Extension of Existing Core 2; 23,710 acres); and along the Santa Ana River (9,670 acres). The total acreage of Core Areas within Criteria Area and Public/Quasi-Public Lands is 81,160 acres. The Core Areas must support a breeding population of approximately 120 burrowing owls combined total (but no fewer than 5 pairs in any one Core Area). Other burrowing owl locations within areas that do not consist of a Core Area also will be conserved within the MSHCP Conservation Area including: the vicinity of Alberhill, between San Jacinto River and Lakeview Mountains, along Santa Gertrudis Creek and Tucalota Creek, and Steele Peak, Sycamore Canyon Regional Park, and the Badlands.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
BURROWING OWL
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| Riverside Lowland Bioregion | |||||||
| Primary Habitat | |||||||
| Grassland | 109,960 | 12,820 | 14,650 | 27,470 | 5,650 | 76,840 | 82,490 |
| Subtotal Primary Habitat | 109,960 | 12,820 (12%) |
14,650 (13%) |
27,470 (25%) |
5,650 (5%) |
76,840 (70%) |
82,490 (75%) |
| Secondary Habitat | |||||||
| Agriculture (field crops) | 115,650 | 5,590 | 9,820 | 15,410 | 490 | 99,750 | 100,240 |
| Playas and Vernal Pools | 7,870 | 3,820 | 2,890 | 6,710 | 0 | 1,160 | 1,160 |
| Subtotal Secondary Habitat | 123,520 | 9,410 (8%) |
12,710 (10%) |
22,120 (18%) |
490 (<1%) |
100,910 (82%) |
101,400 (82%) |
| TOTAL | 233,480 | 22,230 (9%) |
27,360 (12%) |
49,590 (21%) |
6,140 (3%) |
177,750 (76%) |
183,890 (79%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
Available data is not adequate to fully determine the distribution of burrowing owls in the MSHCP Conservation Area or how much conservation the MSHCP Conservation Area will provide. In addition, individual burrowing owl pairs in the Plan Area may be important to the conservation of the species in the Plan Area and Take of individuals will be minimized. Therefore, objectives have been incorporated into the conservation strategy for this species, and are summarized below, to provide assurance of protection and management of a suitable number of known and future localities to conserve this species. Minimization efforts are focused at actively and/or passively relocating burrowing owls from development areas to appropriate MSHCP Conservation Area lands.
Surveys for western burrowing owl will be conducted as part of the project review process for public and private projects within the Criteria Area where suitable habitat is present (see Burrowing Owl Survey Area Map, Figure 6-4 of the MSHCP, Volume I). The locations of this species determined as a result of survey efforts shall be conserved in accordance with procedures described within Section 6.3.2, MSHCP, Volume 1 and the guidance proved below:
Burrowing owl surveys shall be conducted utilizing the protocols identified in the CDFG Staff Report on Burrowing Owl Mitigation. If burrowing owls are detected on the project site then the action(s) taken will be as follows: If the site is within the Criteria Area, then at least 90 percent of the area with long-term conservation value will be included in the MSHCP Conservation Area. Otherwise:
- If the site contains, or is part of an area supporting less than 35 acres of suitable habitat or the survey reveals that the site and the surrounding area supports fewer than three pairs of burrowing owls, then the on-site burrowing owls will be passively or actively relocated following accepted protocols.
- If the site (including adjacent areas) supports three or more pairs of burrowing owls and supports greater than 35 acres of suitable habitat and is non-contiguous with MSHCP Conservation Area lands, at least 90 percent of the area with long-term conservation value and burrowing owl pairs will be conserved onsite.
The survey and conservation requirements stated in this objective will be eliminated when it is demonstrated that Objectives 1 – 4 have been met.
Pre-construction presence/absence surveys for burrowing owl will be conducted for all Covered Activities through the life of the permit. Surveys will be conducted within 30 days prior to disturbance. Take of active nests will be avoided. Passive relocation (use of one way doors and collapse of burrows) will occur when owls are present outside the nesting season.
Translocation sites for the burrowing owl will be created in the MSHCP Conservation Area for the establishment of new colonies. Translocation sites will be identified, taking into consideration unoccupied habitat areas, presence of burrowing mammals to provide suitable burrow sites, existing colonies and effects to other Covered Species. The Wildlife Agencies will concur with the site selection prior to translocation site development.
MSHCP Conservation Area Configuration Issues
Several large blocks of habitat supporting the current known and potential foraging and nesting locations of the burrowing owl will be conserved as MSHCP Conservation including the Lake Skinner/ Diamond Valley Lake area, playa west of Hemet, Lake Perris/Mystic Lake area, Lake Mathews, and Santa Ana River area, and more isolated locations are preserved in the large blocks of habitat at Alberhill, Sycamore Canyon Regional Park, Badlands, Motte-Rimrock Reserve, Steele Peak, Vail Lake, and Wilson Creek with smaller areas preserved in Antelope Valley. Additional areas that provide potential habitat include Lake Elsinore grasslands, Sedco Hills, Box Springs Mountain, Lakeview Mountains, Sage, and foothills of the national forest lands. As identified below, the species occurs within the MSHCP Area Plan as a breeding and wintering resident and as such, the MSHCP Conservation Area will provide adequate habitat for foraging and breeding. These MSHCP Conservation Area areas are linked as well, however the burrowing owl, due to its ability to move long distances and semi-migratory status within the Area Plan, may rely less on the linkages than other species.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 27,470 acres of suitable primary Conserved Habitat and 22,120 acres of suitable secondary Conserved Habitat and 5 of 6 Core Areas within large blocks of habitat in the MSHCP Conservation Area. In addition, 16 recent and high precision locations will be inside the Criteria Area or Public/Quasi-Public Lands. Conservation also will be provided for the habitat linkages between Core Areas and areas important for dispersal as described above. The current population size of the burrowing owl is unknown, however the foraging and nesting habitat requirements are well defined. Surveys will be conducted and locations of owls will be conserved in accordance with procedures described in Section 6.3.2, MSHCP, Volume 1. The Conservation Strategy of this species includes pre-construction surveys of potential habitat areas and conservation as appropriate until sufficient conservation is attained because it occurs in grassland habitats that are not relatively abundant within the MSHCP Conservation Area and the distribution of the species within the Plan Area is not well known. These surveys will provide the information to determine whether the area is currently being used by the species and will supplement the known locations. Translocation of burrowing owls may be used if necessary to establish colonies in currently unoccupied areas.
INCIDENTAL TAKE
The Incidental Take of the burrowing owl is difficult to quantify due to our limited knowledge of its distribution within the Plan Area and the fact that losses may be masked by fluctuations in abundance and distribution during the life of the permit. However, the maximum level of Take of burrowing owl can be anticipated by the loss of the number of acres of habitat that will become unsuitable for this species. About 82,490 acres (75 percent) of the primary potential habitat for the burrowing owl will be outside of the Criteria Area or Public/Quasi-Public lands and individuals within these areas are subject to Incidental Take consistent with the Plan. About 101,400 acres (82 percent) of the secondary potential habitat for the burrowing owl will be outside of the Criteria Area or Public/Quasi-Public Lands and individuals within these areas are subject to Incidental Take consistent with the Plan. A total of 22 point localities recorded within the UCR database will be outside of the MSHCP Conservation Area. Core Areas not conserved include Valle Vista. Smaller numbers of clustered locations of burrowing owls that will be outside the Criteria Area and Public/Quasi-Public Lands, include those locations at the area west of the Jurupa Mountains, San Jacinto, Rancho California area (Long Canyon and De Portola Road), and March ARB. Historically, there were a number of locations concentrated within the Moreno Valley area, however due to the age of the location and the development within the area, the number currently within this area is unknown and receives no conservation within the MSHCP Conservation Area. Individual locations that are outside the MSHCP Conservation Area include locations at Beaumont, Banning, and Murrieta.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The UCR location database includes approximately 109 records for the western burrowing owl within the Area Plan dated from 1887 to 1999. Approximately 82 records are relatively recent (within the past 10 years) and of these recent records, 38 are high precision records that can be accurately placed within the area. The habitat types associated with these recent and high precision data records include residential, riparian (probably represents grassland at the edge of a drainage), grassland, coastal sage scrub, alkali playa, and crop lands. The residential habitat records may reflect records that are either no longer extant or where the location is a small pocket of suitable habitat within or adjacent to a developed area. The locations are predominantly recorded for crop land habitats within the Area Plan. Breeding locations have not been identified within the UCR database, however, due to the sedentary nature of the species, locations are likely near a breeding location.
The literature available on the burrowing owl is relatively large. It is focused on the natural history of the species, and also includes physiological studies and management studies including a trapping and relocation protocol. Several general ornithological reference treatments have been prepared for the species and it has been treated within the general raptor literature. A summary of available information as well as proceedings from a symposium (Lincer and Steenhof 1997) provides substantial information for the species, only a small part of which is presented within this species account. Little information is available with respect to the Area Plan other than general distribution and occurrence information.
Habitat and Habitat Associations
The burrowing owl occurs in shortgrass prairies, grasslands, lowland scrub, agricultural lands (particularly rangelands), prairies, coastal dunes, desert floors, and some artificial, open areas as a year-long resident (Haug, et al. 1993). They may also use golf courses, cemeteries, road allowances within cities, airports, vacant lots in residential areas and university campuses, fairgrounds, abandoned buildings, and irrigation ditches (Haug, et al. 1993; Hayworth 1990 pers. obs.). They may also occur in forb and open shrub stages of pinyon-juniper and ponderosa pine habitats (Zeiner, et al. 1990). They require large open expanses of sparsely vegetated areas on gently rolling or level terrain with an abundance of active small mammal burrows. As a critical habitat feature need, they require the use of rodent or other burrows for roosting and nesting cover. They may also dig their own burrow in soft, friable soil (as found in Florida) and may also use pipes, culverts, and nest boxes where burrows are scarce (Robertson 1929). The mammal burrows are modified and enlarged. One burrow is typically selected for use as the nest, however, satellite burrows are usually found within the immediate vicinity of the nest burrow within the defended territory of the owl.
Biogeography
The burrowing owl breeds from southern interior British Columbia (nearly extirpated), southern Alberta, southern Saskatchewan (extirpated from a portion of the province), and southern Manitoba (extirpated from a portion of the province), south through eastern Washington, central Oregon, and California to Baja California, east to western Minnesota, northwestern Iowa, eastern Nebraska, central Kansas, Oklahoma, eastern Texas, and Louisiana, and south to central Mexico. The winter range is much the same as the breeding range, except that most burrowing owls apparently vacate the northern areas of the Great Plains and Great Basin (Haug, et al. 1993). The burrowing owl winters south regularly to El Salvador (e.g., AOU 1998).
Historical changes in the distribution of the burrowing owl include the recent extirpation from British Columbia for which the last confirmed sighting was in 1979. Elsewhere is Canada and the north-central U.S., the range has contracted slightly southward, westward, and eastward (Haug et al. 1993). In Florida, the range has expanded northward, nearly to Georgia since the 1950s (Courser 1979).
Zeiner et al. (1990) describe the distribution, abundance, and seasonality of the burrowing owl within California as follows. It is a year-long resident formerly common in appropriate habitats throughout the state, excluding the humid northwest coastal forests and high mountains. It is present on the larger offshore islands and is found as high as 1,600 m (5,300 ft) in Lassen County. In California, burrowing owls are restricted to the central valley extending from Redding south to the Grapevine, east through the Mojave Desert and west to San Jose, the San Francisco Bay area, the outer coastal foothills area which extend from Monterey south to San Diego and the Sonoran desert (Grinnell and Miller 1944). It is a resident in the open areas of the lowlands over much of the southern California region (Garrett and Dunn 1981). It is greatly reduced in number within the lowlands of Riverside County and appears to be resident within the region although there is some movement of more northerly birds into the southern and coastal parts of the region (Garrett and Dunn 1981).
Known Population Within Western Riverside County
Within Western Riverside County, the burrowing owl occurs within the central portion within the open lowlands (Garrett and Dunn 1981). It has a sparsely scattered distribution throughout the Area Plan outside of the montane areas. Breeding and burrow locations have not been identified within the UCR database, although most observations that have been recorded are probably located near a burrow due to the relatively sedentary habits of the species.
The species has been detected east of the Jurupa Mountains, along the Santa Ana River, at Lake Mathews, at Good Hope, Alberhill, Murrieta, March Air Reserve Base, the Lake Perris/Mystic Lake area, the Badlands, within the vicinity of Beaumont and Banning, San Jacinto, Valle Vista, between San Jacinto River and Lakeview Mountains, west of Hemet, the area around Diamond Valley Lake, east and south of Lake Skinner area, along Santa Gertrudis Creek and Tucalota Creek, in Long Canyon, and along De Portola Road as documented in the UCR database and from other sources (USFWS 1996 unpublished data; California Science and Engineering Associates 1996).
Based on the information above, clusters of locations, and information from the USFWS (1996 unpublished data), the Core Areas may include Santa Ana River, Lake Mathews area, Lake Perris/Mystic Lake, playa west of Hemet, Lake Skinner/Diamond Valley Lake area, and Valle Vista. Smaller numbers of clustered locations include the area west of the Jurupa Mountains, San Jacinto, Rancho California area (Long Canyon and De Portola Road), and March ARB. Historically, there were a number of locations concentrated within the Moreno Valley area, however due to the age of the location and the development within the area, the number currently within this area is unknown.
Biology
Genetics: The burrowing owl has been variously placed in the monotypic genus Speotyto or in Athene, where it has three congeners (Haug, et al. 1993). Comparison with other karyotypes in the literature suggests that the burrowing owl should be in a separate genus, Speotyto, as has been done for a number of years although it is frequently still referred to as Athene (Schmutz and Moker 1991).
Diet and Foraging: The burrowing owl is a crepuscular hunter with a prey base including invertebrates and small vertebrates (Thomsen 1971). They may hunt by using short flights, running along the ground, hovering or by using an elevated perch from where prey is spotted. They typically forage in short-grass, mowed, or overgrazed pasture, golf courses and airports (Thomsen 1971).
They are a relatively opportunistic forager (Haug, et al. 1993). Their diet is composed of a variety of foods included Peromyscus, Microtus and beetles. Beetles occur within their diet with more frequency, however, based on biomass, Peromyscus is dominant with Microtus appearing second in overall biomass (Marti 1974). Although they eat mostly insects and small mammals, they also may take reptiles, birds, and carrion. During the breeding season, there are significant declines in the percentage of vertebrate prey in the diet and increases in the invertebrate prey (Haug, et al. 1993).
Daily Activity: The burrowing owl is primarily a diurnal species with crepuscular hunting habits (Thomsen 1971). They may move the location of their perch in order to thermoregulate by perching in open sunlight in early morning and then moving to shade or to the burrow, when temperatures are hot (Coulombe 1971).
Reproduction: The burrowing owl usually nests in an old burrow of a ground squirrel, or other small mammal, and may also use the burrow of badgers and marmots. It may dig its own burrow in soft soil. The nest chamber is lined with excrement, pellets, debris, grass, feathers; sometimes it is unlined. Pipes, culverts, and nest boxes are used where burrows are scarce (Robertson 1929). The male gives a courtship display and notes in front of the burrow. Breeding occurs from March through August, with a peak in April and May. The clutch size is 6-11 eggs, with an average of 7-9 eggs; this clutch size may increase to the north (Bent 1938). The young emerge from the burrow at about two weeks, and they fly by about four weeks (Zarn 1974). Martin (1973) reported 95 percent of the young fledged, and a mean reproductive success of 4.9 young per pair. The species is semi-colonial; it is probably the most gregarious owl in North America.
Nest success was 50 to 57 percent at a site in Oregon with desertion being the major cause of nest failures and typically was related to the proximity to other nesting pairs. Burrow sites with good horizontal visibility and little grass coverage were preferred. Elevated perches were used in habitat with average vegetation height greater than 5 centimeters and not in habitats with vegetation less than 5 centimeters. The elevated perches presumably improved the burrowing owl's ability to detect both predators and prey by increasing their horizontal visibility (Green and Anthony 1989). MacCracken et al. (1985) found that nest burrows were in soils with a greater sand content than non-nest burrows, suggesting that selection for soil type may occur. All nest burrows found to be reused in a study in Oregon were in silty loam (Green 1983).
Survival: The minimum annual survival rates in Florida average 68 percent for adult males, 59 percent for adult females and 19 percent for one year old owls (Millsap and Bear 1992). In southern California, the apparent survival rates are 30 percent for juveniles and 81 percent for adults (Thomsen 1971). One banded bird survived to 8 years 8 months (Kennard 1975). Collisions with autos may be a significant cause of mortality (Remsen 1978).
Dispersal: A total of 92 percent of 555 owls that were banded at a nesting area were never re-encountered after the year in which they were banded. The 8 percent that returned to the natal area after being banded, returned one or more years after banding and stayed in the natal area for 2 to 4 breeding seasons (Lutz and Plumpton 1999). Returns of one year old owls were located 2.4 to 26.4 kilometers from the natal nest (Haug et al. 1993).
Socio-Spatial Behavior: The home range may vary from 0.1 to 4 acres (mean is 2 acres) with an average distance between burrows of 436 feet (Thomsen 1971, Martin 1973). Territory size is directly proportional to the available habitat and burrow availability (Haug et al. 1993).
Community Relationships: Predators include prairie falcons, red-tailed hawks, Swainson's hawks, ferruginous hawks, northern harriers, golden eagles, foxes, coyotes, and domestic dogs and cats (Martin 1973). Fleas, lice, and feather mites are common ectoparasites (Zeiner et al. 1990).
They require an abundance of active small mammal burrows. The availability of numerous small mammal burrows is a major factor in determining whether an area with apparently suitable habitat will support burrowing owls (Coulombe 1971). Burrowing owls rarely use areas unoccupied by colonies of burrowing mammals (Zarn 1974).
Potential competition with other owl species is avoided by the burrowing owls habit of hunting at a crepuscular time period and using other prey species including insects in their diets (Marti 1974).
Threats to Species
The threats to the burrowing owl include conversion of grassland to agriculture, other habitat destruction, predators, collisions with vehicles, and pesticides/poisoning of ground squirrels (Grinnell and Miller 1944, Zarn 1974, Remsen 1978). A ranking by the resource agencies of the most important threats to the species included loss of habitat, reduced burrow availability due to rodent control, and pesticides (James and Espie 1997).
The burrowing owl was formerly common in appropriate habitats throughout the state, excluding the humid northwest coastal forests and high mountains. Population numbers have markedly reduced in recent decades (James and Ethier 1989; Zeiner et al. 1990). The primary threats to the species include the loss of natural habitat due to urban development and agriculture and the expressed effects of insecticides and rodenticides within occupied habitat. The use of insecticides may reduce the availability of their primary prey. Pesticides may have secondary adverse effects through contamination. The pesticide Carbofuran has been demonstrated to have negative impacts; Sevin is likely a safer pesticide (Hjertaas et al. 1995; Blus 1996). The loss of burrowing mammal colonies (due to rodenticides or other means) and the crushing of burrows by heavy equipment and ground maintenance machinery remain problematic. This species is usually associated with flat or shallow slopes on loamy soils; these areas are also attractive to agriculture, as well as residential and industrial development. Shooting losses may be significant (Remsen 1978).
The burrowing owl received official status as Endangered in Canada as of 1986. Burrowing owls have gone from locally common to virtually extirpated in Minnesota in 50 years (Johnsgard 1988). The number of burrowing owl breeding pairs in central, western, and southern California have drastically declined in the last 50 years; during the 1980's the decline was probably greater than 70 percent (DeSante and Ruhlen 1995). The species appears to be seriously threatened with extirpation from central, western, and southern California because of the extent and intensity of development (DeSante and Ruhlen 1995).
Special Biological Considerations
Physiological ecology studies have shown that the burrowing owl is able to dissipate 135 percent of their heat production by use of pulmocutaneous evaporation facilitated by gular flutter. This allows the species to use areas that may have air temperatures greater than their body temperature. They also were found to have different emissivities of their feathers depending on the season of year. During the winter, the emissivity of the plumage is greater thus allowing them to augment their metabolic heat production with solar radiative heat gain (Coulombe 1970).
The importance of retaining colonies must be stressed, as this species appears to have evolved as a colonial species in association with burrowing mammal communities (Dyer 1987). Minimum viable colony size is unknown. While these owls appear to adapt fairly well to human presence in some cases, i.e., airport runways and other human modified open spaces, the continued presence of active mammal-created burrows is essential. In Oklahoma, the removal of prairie dogs allowed deterioration of burrows, making them unsuitable for nest burrows after one year (Butts 1973). Rodent eradication programs may reduce the consistent availability of high and moderate function habitat. The remaining habitat is often roadside drainage ditches, increasing potential for significant losses to vehicle collisions (Remsen 1978). The available soil type appears to be a factor in nest burrow selection (see Reproduction section above).
The burrowing owl was shown to choose moderately to heavily grazed grasslands for nesting and roosting and avoided cultivated fields. Where grassland patches were isolated in cultivation areas, the owls dispersed late, for shorter distances and less often. Mortality rate has been shown to be high in these systems. These changes from pasture to cultivation appear to be resulting in a decline of the species (Clayton and Schmutz 1999). It is also important to determine what type and where within the region owls are selecting burrows before the area is disturbed and before it is decided to provision them with artificial burrows. Burrowing owls produced fewer young when occupying a new burrow, and when using burrows in disturbed areas. They produced more young when using artificial burrows but produced fewer fledglings than natural burrows, thus the actual productivity decreased for the artificial burrows (Botelho and Arrowood 1998).
The role of food in limiting the number of offspring fledged from nests has been experimentally investigated in the burrowing owl (Wellicome 1997). Food-supplemented owls laid slightly larger clutches and produced eggs of higher volume but did not show higher hatching success or produce more hatchlings than did the unsupplemented birds. Therefore, although food intake may restrict the number of eggs that burrowing owls lay, the total number of young produced at a nest is constrained by food only during the nestling period. Food intake is thus more limiting during brood rearing than during egg laying (Wellicome 1997).
Urban sites can act as unintentional preserves and support owl populations if habitat features necessary for owls are provided. This is supported by the documented population at Moffett Field in Santa Clara County California. The population has established itself and is using nest burrows under cement or other hard surfaces. The adult density, number of young fledged or pairs with emergent young is not different at Moffett Field compared to other intentional preserve areas (Trulio 1997).
Human activities have had a beneficial effect in Florida where mowing, grazing of cattle and wetland drainage have increased the species' range. Residential and industrial areas currently support the largest concentrations of the species in Florida (Haug et al. 1993).
Because of the intense pressure for urban development within suitable burrowing owl nesting and foraging habitat in California, conflicts between owls and development projects often occur. Owl survival can be adversely affected by disturbance and foraging habitat loss even when impacts to individual birds and nest/burrows are avoided (CDFG 1995). The Staff Report on Burrowing Owl Mitigation (CDFG 1995) outlined the protocol for determining impact assessment. The project site and a 150-meter buffer should be surveyed according to the survey protocol and impacts to the owl should be considered to occur if there is disturbance within 50 meters of a burrow, or there is destruction of natural or artificial burrows, or there is destruction of foraging habitat within 100 meters of a burrow. Mitigation measures should include the provision of 6.5 acres of foraging habitat per pair, provision of two burrows for each burrow impacted, relocation of owls (Trulio 1995), and avoidance of the nesting season.
Given the extraordinary, precipitous decline of this species in cismontane southern California (Grinnell and Miller 1944; Sexton and Hunt 1979; Garrett and Dunn 1981; Hamilton and Willick 1996), it cannot be assumed that preferred habitat patches (e.g., dry, level grasslands and open areas with suitable nesting substrates) within the Area Plan continue to accommodate the species in numbers, similar to those in past years (Grinnell and Miller 1944). For instance, this species, fairly common in the Prado Basin and environs as recently as 1986, is now rare at that locale (Hays 1999 pers. obs.).
The following have been suggested as management strategies (Green 1983): protection of burrowing mammal populations; wood or plastic nest boxes and tunnels; artificial perches which provide hunting and predator observation sites; vegetation management through fire or grazing; and relocation of owls. Other management strategies include: reduce mortality on the breeding grounds, increase productivity, protect and manage the nesting habitat, monitor the populations, manage migration and wintering areas, conduct release programs, and develop public support (Hjertaas 1997).
LITERATURE CITED
AOU (American Ornithologists' Union). 1998. Check-List of North American Birds. Seventh Edition. American Ornithologists' Union, Washington, D.C. 829 pp.
Bent, A. C. 1938. Life histories of North American birds of prey. Part 2. U.S. Natl. Mus. Bull. 170. 482pp.
Botelho, E. S. And P. C. Arrowood. 1998. The effect of burrow site use on the reproductive success of a partially migratory population of western burrowing owls (Speotyto cunicularia hypugaea). J. Raptor Research 32: 233-240.
Blus, L. J. 1996. Effects of pesticides on owls in North America. J. Raptor Research 30: 198-206.
Butts, K. O. 1973. Life history and habitat requirements of burrowing owls in western Oklahoma. Unpublished MS thesis, Oklahoma State University, Stillwater. 188 pp.
California Science and Engineering Associates. 1996. Final threatened and endangered species survey, March Air Reserve Base, Riverside County, California.
California Department of Fish and Game (CDFG). 1995. Staff Report on Burrowing owl mitigation. State of California.
Clayton, K. M and J. K. Schmutz. 1999. Is the decline of burrowing owls, Speotyto cunicularia in prairie Canada linked to changes in the Great Plains ecosystems? Bird Conservation International 9: 163-185.
Coulombe, H. N. 1970. Physiological and physical aspects of temperature regulation in the burrowing owl Speotyto cunicularia. Comp. Biochem. Physiol. 35: 307-337.
Coulombe, H.N. 1971. Behavior and population ecology of the burrowing owl, Speotyto cunicularia, in the Imperial Valley of California. Condor 73: 162-176.
Courser, W. D. 1979. Continued breeding range expansion of the burrowing owl in Florida. Amer. Birds 33: 143-144.
DeSante, D.F. and E.D. Ruhlen. 1995. (draft) A census of burrowing owls in California, 1991-1993.
Dyer, O. 1987. Burrowing owl workshop - Western Raptor Management Symposium: a summary of discussions.
Garrett, K. and J. Dunn. 1981. Birds of Southern California: Status and Distribution. Los Angeles Audubon Society. 407 pp.
Green, G. A. 1983. Ecology of breeding burrowing owls in the Columbia basin, Oregon. M.Sc. Thesis. Oregon State University, Corvallis. 51 pp.
Green, G. A., and R. G. Anthony. 1989. Nesting success and habitat relationships of burrowing owls in the Columbia Basin, Oregon. Condor 91: 347.
Grinnell, J. and A.H. Miller. 1944. The Distribution of the Birds of California. Pacific Coast Avifauna Number 27. Copper Ornithological Club, Berkeley, California. Reprinted by Artemisia Press, Lee Vining, California; April 1986. 617 pp.
Hamilton, R. and D. R. Willick. 1996. The Birds of Orange County, California: Status and Distribution. Sea and Sage Press, Irvine, California. 150 pp. with appendices.
Haug, E. A., B. A. Millsap, and M. S. Martell. 1993. Burrowing Owl (Speotyto cunicularia). In The Birds of North America, No. 130 (A. Poole and F. Gill, Eds.) . Philadelphia: The Academy of Natural Sciences; Washington, D.C.: The American Ornithologists' Union.
Hays, L. R. 1999. USFWS, pers. obs.
Hayworth, A. H. 1990 pers. obs.
Hjertaas, D., S. Brechtel, K. De Smet, O. Dyer, E. Haug, G. Holroyd, P. James, and J. Schmutz. 1995. National Recovery Plan for the Burrowing Owl. Report No. 13. Ottawa: Recovery of the Nationally Endangered Wildlife Committee. 33 pp.
Hjertaas, D. G. 1997. Recovery plan for the burrowing owl in Canada. Journal of Raptor Research Report 9:107-111.
James, P.C., and T. J. Ethier. 1989. Trends in the winter distribution and abundance of burrowing owls in North America. American Birds 43:1224-1225.
James, P.C. and R.H.M. Espie. 1997. Current status of the burrowing owl in North America: an agency survey. Journal of Captor Research Report 9:3-5.
Johnsgard, P. A. 1988. North American owls, biolgoy and natural history. Smithsonian Inst. Press, Washington, D. C.
Kennard, J. H. 1975. Longevity records of North American birds. Bird-banding 46: 55-73.
Lincer, J. L., and K. Steenhof . [eds]. 1997. The burrowing owl, its biology and management: including the Proceedings of the First International Symposium. Raptor Research Report Number 9.
Lutz, R. S., and D. L. Plumpton. 1999. Philopatry and nest site reuse by burrowing owls: implications for productivity. J. Raptor Research 33: 149-153.
MacCracken, J.G., D.W. Uresk, and R.M. Hansen. 1985. Vegetation and soils of burrowing owl nest sites in Conata Basin, South Dakota. Condor 87:152-154.
Marti, C. D. 1974. Feeding ecology of four sympatric owls. Condor 76: 45-61.
Martin, D. C. 1973. Selected aspects of burrowing owl ecology and behavior. Condor 75: 446-456.
Millsap, B. A. and C. Bear. 1992. Double-brooding by Florida Burrowing Owls. Wilson Bull. 102: 313-317.
Pacific Southwest Biological Services. 1991. Western Riverside County Multi-species Habitat Conservation Plan.
Remsen, J. V., Jr. 1978. Bird species of special concern in California. Calif. Dep. Fish and Game, Sacramento. Wildl. Manage. Admin. Rep. No. 78-1. 54pp.
Robertson, J. M. 1929. Some observations on the feeding habits of the burrowing owl. Condor 31: 38-39.
Sexton, C.W. and G.L. Hunt. 1979. An annotated checklist of the birds of Orange County, California. University of California Irvine Museum of Systematic Biology Research Series No. 5.
Schmutz, S. M., and J. S. Moker. 1991. A cytogenetic comparison of some North American owl species. Genome 34: 714-717.
Thomsen, L. 1971. Behavior and ecology of burrowing owls on the Oakland Municipal airport. Condor 73: 177-192.
Trulio, L. A. 1995. Passive relocation: a method to preserve burrowing owls on disturbed sites. J. Field Ornithology 66: 99-106.
Trulio, L. 1997. Burrowing owl demography and habitat use at two urban sites in Santa Clara County, California. Journal of Raptor Research Report 9:84-89.
USFWS. 1996. unpublished data.
Wellicome, T. I. 1997. Reproductive performance of burrowing owls (Speotyto cunicularia): effects of supplemental food. Journal of Raptor Research Report 9: 68-73.
Zarn, M. 1974. Burrowing Owl, Report No. 11. Habitat management series for unique or endangered species. Bureau of Land Management, Denver. 25 pp.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
cactus wren (Campylorhynchus brunneicapillus)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
cactus wren (Campylorhynchus brunneicapillus)
Status:
State: Species of Special Concern
Federal: Cleveland National Forest Sensitive
GROUP DESIGNATION AND RATIONALE
Group 3
The cactus wren is narrowly distributed at relatively few locations in suitable habitat within the Plan Area. Although the preferred habitat, coastal sage scrub, desert scrubs, and Riversidean alluvial fan sage scrub is well distributed, the locations of the cactus wren are clumped in few locations due to its specific habitat requirements. It requires patches of cactus-dominated sage scrub habitat in the Riverside Lowland and San Jacinto Foothill Bioregions of the Plan Area. Because this species has specific habitat requirements (cactus patches), occurs in few locations within a broader habitat category, and occurs in relatively low numbers within the Plan Area, the cactus wren will require site-specific considerations, a landscape level of management, and species-specific conservation measures as a Group 3 species.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 77,070 acres of suitable habitat for the cactus wren including desert scrub, Riversidean alluvial fan sage scrub, and coastal sage scrub within Riverside Lowland and San Jacinto Foothill Bioregions.
Objective 2
Include within the MSHCP Conservation Area at least 11 Core Areas and interconnecting linkages including Chino Hills (Proposed Extension of Existing Core 1; 270 acres), Badlands (Proposed Core 3; 24,920 acres), Box Springs Mountains (Existing Noncontiguous Habitat Block A plus Proposed Constrained Linkages 7 and 8; 4,000 acres), Lake Mathews-Estelle Mountain area (Existing Core C plus Proposed Extension of Existing Core 2; 23,710 acres), Alberhill (Subunit 2 of Elsinore Area Plan; 3,460 acres), Motte-Rimrock area MSHCP Conservation Area (Proposed Noncontiguous Habitat Block 4; 1,150 acres), Lake Perris/Bernasconi Hills (Existing Core H; 17,470 acres), Lake Skinner (Existing Core C plus Proposed Extension of Existing Cores 5, 6, 7; 29,060 acres), Vail Lake (Subunit 3 of Southwest Area Plan; 12,320 acres), Wilson Valley (Subunit 2 of REMAP Area Plan; 33,540 acres), and Aguanga (Subunit 4 of REMAP Area Plan; 2,660 acres).
Objective 3
Include within the MSHCP Conservation Area micro-habitat (i.e., cactus patches) in potential nesting habitat.
SPECIES CONSERVATION ANALYSIS
Conservation and Take Levels
The cactus wren is restricted to cactus-dominated stands of coastal sage scrub below 457 meters in elevation on mesas and lower slopes of the coast ranges (Proudfoot et al. 2000). For the purpose of the conservation analysis and based on the matching of the distribution of the species with the appropriate Bioregions, potential habitat for the cactus wren includes desert scrubs, Riversidean alluvial fan sage scrub, and coastal sage scrub within the Riverside Lowland and San Jacinto Foothills Bioregions. Based on these habitats, the Area Plan supports approximately 140,770 acres of potential habitat for the cactus wren. Table 1 shows the conservation and loss of potential habitat for the cactus wren. Overall, approximately 77,070 acres (55 percent) of potential habitat in the Area Plan will be conserved in Criteria Area or existing Public/Quasi-Public Lands. Although the habitats used in this analysis includes more acreage than is considered suitable habitat, the cactus-dominated sage scrub is imbedded within the broader categories of habitat. Mapping of cactus-dominated sage scrub is not available for the Area Plan.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
CACTUS WREN
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| Riverside Lowlands and San Jacinto Foothills Bioregions | |||||||
| Desert Scrubs | 2,230 | 2,160 | 0 | 2,160 | 40 | 30 | 70 |
| Riversidean Alluvial Fan Sage Scrub | 5,430 | 2,710 | 1,310 | 4,020 | 160 | 1,250 | 1,410 |
| Coastal Sage Scrub | 133,110 | 43,690 | 27,200 | 70,890 | 19,740 | 42,480 | 62,220 |
| TOTAL | 140,770 | 48,560 (34%) |
28,510 (20%) |
77,070 (55%) |
19,940 (14%) |
43,760 (31%) |
63,700 (45%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
As described below under Data Characterization, 34 of the 70 recent point localities have a high location precision. Of these 34 point localities, 14 will be inside the Criteria Area or Public/Quasi-Public Lands. A total of 20 point localities will be outside of the MSHCP Conservation Area or within Rural/Mountainous designations. Conservation of this species will be considered from a landscape perspective, as discussed above because the species has well defined habitat requirements. Additionally, there are definable locations of Core Areas for focusing conservation efforts where the species is observed in larger numbers.
The conserved Core Areas include the suitable and occupied habitat within the Criteria Area and Public/Quasi-Public designations in the Chino Hills (Proposed Extended Existing Core 1; 270 acres), Badlands (Proposed Core 3; 24,920 acres), Box Springs Mountains (Existing Noncontiguous Habitat Block A plus proposed Constrained Linkages 7 and 8; 4,000 acres), Lake Mathews-Estelle Mountain Reserve (Existing Core C plus Proposed Extension of Existing Core 2; 23,710 acres), Alberhill (Subunit 2 of Elsinore Area Plan; 3,460 acres), Motte-Rimrock Reserve (Proposed Noncontiguous Habitat Block 4; 1,150 acres), Lake Perris/Bernasconi Hills (Existing Core H; 17,470 acres), Lake Skinner (Existing Core C plus Proposed Extension of Existing Cores 5, 6, 7; 29,060 acres), Vail Lake (Subunit 3 of Southwest Area Plan; 12,320 acres), Wilson Valley (Subunit 2 of REMAP Area Plan; 33,540 acres), and Aguanga (Subunit 4 of REMAP Area Plan 2,660 acres). The total acreage of Core Areas within Criteria Area and Public/Quasi-Public Lands is 152,560 acres. Some additional locations of cactus wrens will be conserved within the Sycamore Canyon Regional Park, Cactus Valley, and Bautista Creek.
The Chino Hills Core Area continues into Orange County where the population also occurs. The Badlands Core Area is located in the vicinity of Lamb Canyon Road and continues north along Gilman Hot Springs Road. The Lake Perris Core Area is within the low hills between the San Jacinto Wildlife Area and Mystic Lake and within the Bernasconi Hills. The Lake Mathews-Estelle Mountain Reserve Core Area is predominantly south of Cajalco Road. The Vail Lake/Wilson Valley Core Area occurs within a broad expanse from east of Vail Lake into the Wilson Creek area, along Sage Road, and north within Wilson Valley. The Aguanga Core Area is within the Temecula Creek drainage south of State Route 79.
Conservation of the cactus wren also requires species-specific conservation measures due to the low abundance of the species within the Plan Area and the specific habitat requirements which include large patches of cactus used for breeding and foraging. Recently, there have been examples within southern California of cactus wren population declines from the destruction of large patches of cactus by fire (Bontrager et al. 1995). These populations of the cactus wren have not recovered well. The species-specific conservation measure for the cactus wren consists of conserving the microhabitat for this species which is composed of cactus patches within the Core Areas within the MSHCP Conservation Area via a number of methods that may include fire suppression (Proudfoot et al. 2000), enhancement, or revegetation with cacti.
MSHCP Conservation Area Configuration Issues
Several large blocks of habitat supporting the current known nesting and foraging locations, and potential foraging and nesting locations of the cactus wren will be conserved as Criteria Area and Public/Quasi-Public categories, including the Chino Hills, Badlands, Box Springs Mountains, Alberhill, Lake Mathews-Estelle Mountain Reserve, Motte-Rimrock Reserve, Lake Perris/ Bernasconi Hills, Lake Skinner, Vail Lake, Wilson Valley, and Aguanga. Additional areas that may have isolated cactus wren locations that may or may not be extant, but that may provide potential habitat, include the Santa Rosa Plateau Nature Reserve where a low precision point is located, Prado Basin, Santa Ana River, Fresno Canyon Creek, Bautista Creek, and Cactus Valley. As identified above, the species occurs within the MSHCP Plan Area as a nesting, foraging, and wintering species, and, as such, the MSHCP Conservation Area will provide adequate habitat for all phases of the life history. Habitat containing potential nest sites with adequate protection around each nest site will also be conserved. These MSHCP Conservation Area locations are linked as well, providing dispersal connections between the southern locations at Aguanga and eastern Temecula Creek into San Diego County, along Temecula Creek into the Cleveland National Forest and Santa Rosa Plateau, north from Wilson Valley to the Lake Skinner/Diamond Valley Lake area, north along Bautista Creek into the Badlands and then into San Bernardino County or to Lake Perris area or the Box Springs area. Linkages are provided from Lake Skinner to the Sedco Hills through the Tucalota and Warm Springs drainages and the AD161 Mitigation Area. Habitat patches are then connected to the Santa Ana River via the Sedco Hills and Temescal Wash. Most of these linkages are connected by patches of coastal sage scrub except for those along the drainages which are currently constrained but provide riparian habitat for use as dispersal habitat. The cactus wren is a relatively sedentary species, thus conservation of its preferred habitat with a focus on the microhabitat is very important (Garrett and Dunn 1981). However, vagrants have been observed away from known breeding areas in other regions, consequently, the MSCHP Conservation Area design will provide for connections between Core Areas to provide for the potential for movement of this species (Garrett and Dunn 1981).
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 77,070 acres of suitable Conserved Habitat and 11 of 12 Core Areas within large blocks of habitat in the MSHCP Conservation Area. In addition, 14 recent and high precision locations will be inside the Criteria Area or Public/Quasi-Public Lands, all of which are recorded for the suitable habitat of the cactus wren. Conservation also will be provided for the habitat linkages between Core Areas as identified above. Additionally, the species-specific conservation measure for the cactus wren consists of conserving the microhabitat for this species which is composed of cactus patches within the Core Areas within the MSHCP Conservation Area. The current population size of the cactus wren is unknown but has been estimated at 100 to 110 pairs (McKernan 1998 pers. comm.).
INCIDENTAL TAKE
The Incidental Take of the cactus wren is difficult to quantify due to our limited knowledge of its distribution and abundance within the Plan Area. The maximum level of Incidental Take of cactus wrens can be anticipated by the loss of the number of acres of potential habitat that will become unsuitable for this species. About 63,700 acres (45 percent) of potential habitat for the cactus wren will be outside the Criteria Area and Public/Quasi-Public designations, and individuals within this habitat will be subject to Incidental Take consistent with the plan. Of this, approximately 19,940 acres of potential habitat (14 percent) are located within Rural/Mountainous designation areas. While the Rural/Mountainous areas are not included within the MSHCP Conservation Area, will not be managed for the benefit of wildlife, and the existing zoning/ordinances for these areas do not preclude development and could allow substantial fragmentation and/or degradation of habitat for proposed covered species, the anticipated levels of development of these areas may be consistent with maintaining some habitat for the cactus wren. A total of 20 locations within the UCR database of the cactus wren will be outside the Criteria Area and Public/Quasi-Public designations, 9 of which are located within residential or developed areas and may no longer be extant. The Core Area within the Temecula Creek area west of Vail Lake is not considered conserved. Although a Proposed Constrained Linkage is located within this drainage, the upland areas within which the cactus wren might be present are not conserved.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature. The location database for the cactus wren includes approximately 75 data records from 1888 to 1999. Of these records, approximately 70 are relatively recent (within the past 10 years) and of these, 34 are of high precision and may be accurately located within the Plan Area. Approximately 10 of these high precision records are located within developed areas and although they may no longer exist, they may also represent an observation of a cactus wren within a localized patch of cactus that is within near proximity of a residential development. The rest occur within non-native grassland, sage scrub, chaparral, and other vegetation communities that are likely located within cactus-dominated patches of coastal sage scrub that may be mapped within other vegetation types. The database does not identify those records that are breeding locations or indicate the overall population size.
A low to moderate amount of literature is available for the cactus wren because of its interesting habitat use and natural history. Most of the literature pertains to general natural history, niche determination, and detailed information regarding the nest structure. Few controlled scientific studies have been conducted; however, some management studies are available. Very little information is available for the Plan Area other than what is generally available regarding basic distribution information.
Habitat and Habitat Associations
The cactus wren is an obligate, nonmigratory resident of the coastal sage scrub plant community (as defined by Westman 1983 and O'Leary 1990). It frequents deserts and other arid terrain with thickets, patches, or tracts of larger, branching cacti, stiff-twigged, thorny shrubs, and small trees (Grinnell and Miller 1944). In other areas, it is considered an inhabitant of the Chihuahuan, Mojave, and Sonoran deserts and Tamaulpais thorn-shrub communities. It may also be considered a resident of scrubby flats, cactus and mesquite lowland areas, brushy mesas, gulches, hills, and canyons in Texas, desert riparian, creosote bush and large arroyos in Nevada (Proudfoot et al. 2000). It is closely associated with three species of cacti and occurs almost exclusively in thickets of cholla (Opuntia prolifera) and prickly pear (Opuntia littoralis and Opuntia oricola) dominated stands of coastal sage scrub below 457 meters in elevation on mesas and lower slopes of the coast ranges (Proudfoot et al. 2000). Although it lives over a wide range from Texas to the Pacific ocean, it is limited to regions with thorny shrubs and trees that offer nesting sites (Terres 1980).
Characteristic shrubs associated with habitat occupied by the cactus wren and within the coastal sage scrub community include California buckwheat (Eriogonum fasiculatum), coastal sagebrush (Artemisia californica), several sages (Salvia spp.) and scattered shrubs approaching tree-size, such as laurel sumac (Malosma laurina), and lemonadeberry (Rhus integrifolia) (Garrett and Dunn 1981, Unitt 1984, Rea and Weaver 1990). Thickets of xeric vegetation may provide cover and thermal relief. The nest is also used as a roost site (Anderson and Anderson 1957).
Biogeography
The cactus wren is a resident species from southern California south to southern Baja California, southern Nevada, southwestern Utah, western and south central Arizona, southern New Mexico, and central Texas south to Mexico (Terres 1980).
Zeiner, et al. (1990) summarize the distribution, abundance, and seasonality of the cactus wren in California as follows. It is a locally common resident in the Mojave and Colorado deserts, north from the Mexican boundary to Inyo and Kern counties. The coastal race is found in arid parts of westward-draining slopes from San Diego County northwest to Ventura County. It frequents desert succulent shrub, Joshua tree, and desert wash habitats. Historically, cactus wrens within coastal areas were found on the coastal slopes and lowlands of southern California in arid and semiarid regions with abundant cacti (Grinnell 1898, Grinnell and Miller 1944 Unitt 1984). As early as 1944, authorities noted that loss of habitat had greatly reduced the historic range of this species (Grinnell and Miller 1944).
Known Populations Within Western Riverside County
The cactus wren is found at few locations within the Plan Area. It has been recorded along the eastern flank of the Santa Ana Mountains from the vicinity of Corona to Lake Mathews and Alberhill. It also occurs from the city of Riverside east to the Box Springs Mountains and into the Badlands. Small populations also occur in the central portion of the area and Bernasconi Hills near Lake Perris and then disjunctly within the southern portion from Temecula to Aguanga. About 100 to 110 pairs of the cactus wren are estimated to occur in Riverside County (McKernan 1998 pers. comm.).
The Core Areas within the Plan Area consist of a few, small, disjunct populations. Based on the information from Cooper (2001) and the UCR database, as well as the information identified above, the Core Areas are located at the Badlands, Box Springs Mountains, Lake Mathews-Estelle Mountain Reserve, Motte-Rimrock Reserve, Lake Perris area including Bernasconi Hills, Lake Skinner, Vail Lake, Wilson Valley, Aguanga, and Temecula area. These areas appear to be remaining strongholds for low to moderate numbers of the cactus wrens in western Riverside county. The locations of the cactus wren become even more patchy within the central and eastern areas of the county. A Core Area is located within the northwestern section of the county near the Chino Hills adjacent to Orange County where cactus wrens are known to occur within oil fields that have suitable habitat (McKernan 1998 pers. comm.).
Biology
Genetics: The variation in plumage patterns and characters are used to distinguish the subspecies of the cactus wren. Eight subspecies are recognized with the subspecies falling into roughly two groups the affinis group (peninsular forms) and brunneicapillus group (continental forms) (Proudfoot et al. 2000). The range of C. b. cousei is now geographically disjunct from interior desert populations as a result of urbanization of the corridor along the San Gorgonio Pass in Riverside County (Rea and Weaver 1990).
Diet and Foraging: The cactus wren forages on the ground and in low vegetation for insects and other small invertebrates, cactus fruits and other fruits, seeds and nectar (Bent 1968; Anderson and Anderson 1973). Fruits make up 15-20 percent of the annual diet, which is more than most North American wrens (Ehrlich, et al. 1988). Foraging behavior is often regulated by heat stress (Ricklefs and Hainsworth 1968), necessitating retreat from exposed sites into shade of shrubs and trees. The cactus wren generally forages on the ground, turning over fallen leaves and other debris in search of insects. It also searches bushes and probes tree bark housing insects. Foliage-gleaning may increase with insect abundance and habitat complexity (Proudfoot et al. 2000).
Daily Activity: The cactus wren exhibits year-long, diurnal activity. The species is not migratory (Zeiner, et al. 1990).
Reproduction: For the cactus wren, thickets of vegetation provide cover and shelter, and the nest, which is usually located in cactus, is used as a roost site as well as for breeding. The nest is usually built in cholla or other large, branching cactus, in yucca, or in a stiff-twigged, thorny shrub or small tree. The nest is an intricate, woven cylinder, usually placed horizontally 1.2 to 1.5 meters (4-5 feet) above the ground (Anderson and Anderson 1957). The large, globular chamber of the nest is about 18 centimeters in diameter with a tunnel-shaped passageway about 9 centimeters in diameter with as much as 30 centimeters between the back wall of the nest chamber and the entrance opening. The mouth of the entrance is usually about 7 centimeters above the base of the chamber. Because the passageway is too small to admit a flying bird, a doorstep or perch is required near the entranceway (Proudfoot et al. 2000). It breeds from March into June. The clutch size is 4-5 eggs, with a range of 3-7 eggs (Harrison 1978). Two broods per season is common. Incubation is 15-18 days, by the female only (Anderson and Anderson 1960). The altricial nestlings fledge at 17-23 days, with an average of 21 (Hensley 1959, Anderson and Anderson 1960). The young may return to roost in the nest after fledging. The young become independent at about 1 mo after leaving the nest; sometimes the young help feed the young of later broods (Harrison 1978).
Survival: Anderson and Anderson (1973) report an overall adult survival rate of 50.6 percent during a six year study. One banded adult was retrapped when it was 4 years old (Terres 1980).
Dispersal: The species is generally considered to have low dispersal capabilities but there is little information available (Ogden Environmental and Energy Services 1993). In Arizona, of 55 nestlings banded, 41 dispersed from the natal site by 45 days postfledging. Males remain near the natal site, usually dispersing only as far as parental territorial behavior dictated (Proudfoot et al. 2000).
Socio-Spatial Behavior: The home range may be the same as the territory (Anderson and Anderson 1963). The average territory was 1.9 hectares (4.8 acres), varying from 1.2-2.8 hectares (2.9-6.9 acres), in Arizona (Anderson and Anderson 1973). The cactus wren may maintain its territory year-round (Anderson and Anderson 1963).
Community Relationships: Domestic cats, roadrunners, snakes, and loggerhead shrikes prey on adults and nestlings (Anderson and Anderson 1973). Austin, et al. (1972) observed nestling predation by gopher snakes and whipsnakes. Frequent interactions with curve-billed thrashers have been reported by Anderson and Anderson (1963), including destruction of cactus wren roosting nests by thrashers.
Threats to Species
Continued threats to the cactus wren include habitat loss and fragmentation from urbanization and agricultural development. Domestic cats, roadrunners, snakes, and loggerhead shrikes prey on adults and nestlings (Anderson and Anderson 1973). Cactus wrens that are confined to isolated patches of habitat in urbanizing areas are subject to increased levels of predation pressures as larger predators are replaced by greater population levels of smaller predators and domestic animals. This species is especially vulnerable to stochastic events, especially wildland fires. Because of its narrow habitat requirements, sedentary behavior, and low dispersal characteristics, cactus wrens are subject to loss by fires and, if they disperse, may not find suitable habitat to survive. Intense fires may actually kill cactus plants and eliminate habitat for the cactus wren. As a result of competition from invasive plant competition, grazing, weather patterns and other natural and human-influenced disturbances, the reestablishment of cactus patches essential to this species may take many years. An increasing pattern of habitat fragmentation and isolated populations also diminishes the dispersal ability and inter-population connections of the cactus wren and reduces the overall genetic viability of the species (Ogden Environmental and Energy Services 1993).
Special Biological Considerations
The cactus wren is highly associated with cactus thickets in coastal sage scrub and is reliant on cacti for nesting, breeding and foraging. This species has an affinity for cholla cactus as a nesting and roosting site and this plant species is very important to its survival. (Bailey 1922; Grinnell and Miller 1944; Bent 1968; Anderson and Anderson 1973; Root 1988). The recommendations for protecting the cactus wren includes protection and maintenance of large blocks of coastal sage scrub through fire suppression (Rea and Weaver 1990).
Cactus wrens build four to six nests within their territories and thus enumerating the number of nests within an area is not a representative method for sampling population size (Anderson and Anderson 1973).
The cactus wren has been documented to have significant differences in clutch size, breeding success, and the timing of clutch initiation between years (Marr and Ratt 1983). These differences appear to be related to the annual differences in the abundance and emergence of the major food of the nestlings. Long-term temperature patterns may provide a predictor for high prey populations (Marr and Raitt 1983).
A flowchart was developed for the habitat suitability model for the cactus wren (Short 1985). Suitable habitat is evaluated as including: arid savanna, open thorn forest, or semidesert cactus and deciduous tree cover types in southwestern United States; a block of appropriate habitat that is at least 0.4 hectare in area; habitat structure that provides potential nest sites 0.9 to 4.3 meters above ground; types of vegetation that vary in utility as nest sites for the cactus wren; with the density of mid-story vegetation that may modify the utility of habitats for cactus wrens.
LITERATURE CITED
Anderson, A. H., and A. Anderson. 1957. Life history of the cactus wren. Part I: Winter and pre-nesting behavior. Condor 59:274-296.
Anderson, A. H., and A. Anderson. 1960. Life history of the cactus wren. Part III: The nesting cycle. Condor 62:351-369.
Anderson, A. H., and A. Anderson. 1963. Life history of the cactus wren. Part IV: Competition and survival. Condor 65:29-43.
Anderson, A.H. and A. Anderson, 1973. The Cactus Wren. The University of Arizona Press, Tucson, Arizona.
Austin, G. T., E. Yensen, and C. S. Tomoff. 1972. Snake predation on cactus wren nestlings. Condor 74:492.
Bailey, F.M. 1922. Cactus wrens' nests in southern Arizona. Condor 24:163-168.
Bent, A.C. 1968. Life histories of North American Nuthatches, Wrens, Thrashers, and their allies. U.S. National Museum Bulletin 195. U.S. Government Printing Office. Washington, D.C.
Bontrager, D. R., R. A. Erickson, and R. A. Hamilton. 1995. Impacts of the October 1993 Laguna Canyon fire on California Gnatcatchers and Cactus Wrens. Pp. 69-76 In Brushfires in California wildlands: ecology and resource management (J. E. Keeley and T. Scott, eds.). Int. Assoc. Wildland fire, Fairfield, WA.
Cooper, D. 2001. California Important Birding Areas. Audubon California, Los Angeles.
Ehrlich, P. R., D. S. Dobkin, and D. Wheye. 1988. The birder's handbook. Simon and Schuster, New York. 785pp.
Garrett, K. and J. Dunn. 1981. Birds of southern California: status and distribution. Artesan Press, Los Angeles, CA.
Grinnell, J. 1898. Birds of the Pacific slope of Los Angeles County.
Grinnell, J. and A.H. Miller. 1944. The distribution of the birds of California. Pacific Coast Avifauna 27.
Harrison, C. 1978. A field guide to the nests, eggs and nestlings of north American birds. W. Collins Sons and Co., Cleveland, OH. 416pp.
Hensley, M. M. 1959. Notes on the nesting of selected species of birds of the Sonoran Desert. Wilson Bull. 71:86-92.
Marr, T.G. and R.J. Raitt. 1983. Annual variations in patterns of reproduction of the cactus wren (Campylorhynchus brunneicapillus). Southwestern naturalist 28:149-156.
McKernan, Robert. 1998. San Bernardino Natural History Museum. Personal communication.
O'Leary, J. F. 1990. California coastal sage scrub: general characteristics and considerations for biological conservation. Pp. 24-41 in Endangered Plant Communities of southern California. Southern California Botanists Special Publication No.3 (A.A. Schroeder, ed.)
Ogden Environmental and Energy Services. 1993. Population viability analysis for the coastal cactus wren within the MSCP Plan Area. Prepared for the Clean Water Program City of San Diego. 16 pp.
Proudfoot, G. A. , D. A. Sherry, and S. Johnson. 2000. Cactus wren (Campylorhynchus brunneicapillus) No. 558. In The Birds of North America, A. Poole and F. Gill, Eds. Cornell laboratory of Ornithology, New York, and The Academy of Natural Sciences, Washington D.C.
Rea, A.M. and K. L. Weaver, 1990. The taxonomy, distribution, and status of coastal California cactus wrens. Western Birds 21: 81-126.
Ricklefs, R. E., and F. R. Hainsworth. 1968. Temperature dependent behavior of the cactus wren. Ecology 49:227-233.
Root, T. 1988. Atlas of wintering North American birds. An analysis of Christmas bird count data. University of Chicago Press, Chicago IL.
Short, H. L. 1985. Habitat suitability index models: cactus wren. U.S. Fish and Wildlife Service Biological Report 82(10.96).
Termes, J. K. 1980. The Audubon Society Encyclopedia of North American Birds. Alfred A. Knopf, New York, New York. 1109pp.
Unitt, P. 1984. The Birds of San Diego County. San Diego Society of Natural History, San Diego, CA.
Westman, W. E. 1983. Factors influencing the distribution of species of California coastal sage scrub. Ecology 62: 439-455.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
California horned lark (Eremophila alpestris actia)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
California horned lark (Eremophila alpestris actia)
Status:
State: Species of Special Concern
Federal: none
GROUP DESIGNATION AND RATIONALE
Group 2
The California horned lark is relatively widely-distributed throughout the MSHCP Plan Area within its suitable habitat, however, it is not predictably distributed within all suitable areas. It occurs in some of the sparsely vegetated habitats but has not been documented to be uniformly distributed within all open habitat areas. There appear to be several Core Areas including Mystic Lake/San Jacinto Wildlife Area, the grasslands within Prado Basin, Wasson Canyon area, Moreno Valley/March ARB, and Murrieta/Murrieta Hot Springs area. Because it is well known for using open, sparsely vegetated habitats but has specific locations that appear to be Core Areas, it responds well to a landscape level of management with site specific requirements.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 153,750 acres of suitable foraging and nesting habitat for the California horned lark including playa and vernal pool habitats, agriculture (field croplands), grassland, cismontane alkali marsh, coastal sage scrub, and Riversidean alluvial fan sage scrub. The scrub habitats provide foraging habitat and nesting opportunities in areas where the scrub is relatively sparse.
Objective 2
Include within the MSHCP Conservation Area at least 3 Core Areas and a portion of a fourth Core Area for the California horned lark including grasslands around Prado Basin (including the adjacent Santa Ana River area; 9,670 acres), Wasson Canyon (Subunit 5 of Elsinore Area Plan; 2,320 acres), Mystic Lake/San Jacinto Wildlife Area (Subunit 4 of Reche Canyon/Badlands Area Plan; 2,690 acres), and a portion of the Core Area in the Murrieta/Murrieta Hot Springs area (Proposed Core 2; 5,050 acres). Other locations are conserved as well, although they may not include Core Areas. These other locations include Lake Elsinore grasslands, Santa Rosa Plateau, and Wilson Valley.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
The California horned lark uses predominantly open land including agriculture, grassland and playas for foraging as well as sparse shrub and scrub habitats (Garrett and Dunn 1988). The California horned lark breeds, winters ,and migrates throughout the MSHCP Plan Area. For the purpose of the conservation analysis, potential habitat for the California horned lark includes agriculture(field croplands), grassland, cismontane alkali marsh, playa and vernal pool habitat, Riversidean alluvial fan sage scrub, and coastal sage scrub. The scrub habitats are included because they have been recorded foraging and nesting within sparse forms of such habitats and constitute of a Core Area within the scrub habitat in the Wasson Canyon area. The horned lark has been recorded using chaparral and riparian habitat, however these are not typical habitats used by the species. The observation may have been of the species foraging nearby and thus these habitats are not included in the analysis. The habitats included in the analysis comprise open habitat within which they typically forage and nest. Based on these habitats, the Plan Area supports approximately 438,550 acres of potential habitat for the California horned lark. Table 1 shows the conservation and loss of potential habitat for the California horned lark. Overall, approximately 153,750 acres (35 percent) of potential habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public Lands.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
CALIFORNIA HORNED LARK
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| All Bioregions | |||||||
| Agriculture Land (field crops) | 230,370 | 7,250 | 9,940 | 106,590 | 820 | 105,770 | 106,590 |
| Grassland | 146,870 | 20,010 | 22,810 | 42,820 | 12,220 | 91,830 | 104,050 |
| Cismontane Alkali Marsh | 150 | 40 | 0 | 40 | 0 | 110 | 110 |
| Playas and Vernal Pools | 7,910 | 3,830 | 2,920 | 6,750 | 0 | 1,160 | 1,160 |
| Riversidean Alluvial Fan Sage Scrub | 7,150 | 3,170 | 2,060 | 5,230 | 220 | 1,700 | 1,920 |
| Coastal Sage Scrub | 152,690 | 47,160 | 34,560 | 81,720 | 26,240 | 44,730 | 70,970 |
| TOTAL | 438,550 | 81,460 (19%) |
72,290 (16%) |
153,750 (35%) |
39,500 (9%) |
245,300 (56%) |
284,800 (65%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
As described above under Data Characterization, 77 of the 187 recent point localities have a high location precision of "1." Of these 77 point localities, 34 will be inside the Criteria Area or Public/Quasi-Public Lands. A total of 43 point localities will be outside of the MSHCP Conservation Area, 25 percent of which are within residential/developed areas. Three of the five core population areas where the species is observed, (including the adjacent Santa Ana River area; 9,670 acres), Wasson Canyon (Subunit 5 of Elsinore Area Plan; 2,320 acres), Mystic Lake/San Jacinto Wildlife Area (Subunit 4 of Reche Canyon/Badlands Area Plan; 2,690 acres) will be conserved. A fourth Core Area, the Murrieta/Murrieta Hot Springs area, will be conserved in part within the Proposed Core in the Antelope Valley area in the form of the scrub areas north of Clinton Keith Road east to French Valley, the Hogbacks, and east into the AD161 mitigation area (Proposed Core 2; 5,050 acres). Conservation of this species will be considered from a landscape perspective because the species is very flexible and opportunistic for its foraging requirements. Additionally, there are definable locations for focusing conservation efforts where the species is observed in larger numbers within Core Areas. A total of 19,730 acres of Core Areas will be conserved within large habitat blocks of a minimum size of 2,320 acres.
MSHCP Conservation Area Configuration Issues
Several large blocks of habitat supporting the current known and potential foraging and nesting locations of the California horned lark will be conserved as Criteria Area and Public/Quasi- Public lands, including the Prado Basin, Mystic Lake/San Jacinto Wildlife Area, Proposed Core in the Antelope Valley area, and Wasson Canyon. Additional large blocks that contain observations and that provide potential nesting and foraging habitat include Wilson Valley, Santa Rosa Plateau Nature Reserve, and Lake Elsinore grasslands. As identified below, the species occurs within the MSHCP Plan Area as a breeding and wintering resident and as such, the MSHCP Conservation Area will provide adequate habitat for foraging and nest sites. These MSHCP Conservation Area areas are linked as well, however the California horned lark, due to its ability to move long distances, may rely less on the linkages than other species.
Conservation Summary
In summary, conservation for this species will be achieved by the inclusion of at least 153,750 acres of suitable Conserved Habitat and the Core Areas within the Prado Basin, Wasson Canyon, and Mystic Lake/San Jacinto Wildlife Area, as well as a portion of the Core Area within the Murrieta/Murrieta Hot Springs area (Proposed Core 2). The current population size of the California horned lark is unknown however the foraging and nesting habitat requirements are well defined. The species is moderately predictable in its occurrence and may vary in number within the area from a few to many individuals. It occurs repeatedly in a number of conserved locations.
INCIDENTAL TAKE
About 284,800 acres (65 percent) of potential habitat for the California horned lark will be outside the Criteria Area and Public/Quasi-Public designations and individuals within these areas will be subject to Incidental Take consistent with the Plan. One of the 5 Core Areas, the Moreno Valley/March ARB area, will be outside the MSHCP Conservation Area. A portion of a Core Area within the Murrieta/Murrieta Hot Springs area will be outside the MSHCP Conservation Area.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The UCR location database includes approximately 252 records for the California horned lark dated from 1887 to 1999. Approximately 187 of these data records are recent (within the past 10 years) and of these recent records, approximately 77 are of high precision and suitable for analysis. The habitat types associated with these data records are varied: from sage scrub, grassland, chaparral, riparian scrub and willow riparian, alkali playa to more developed habitats including crop lands and residential. Occurrence within residential does not necessarily indicate the species record is no longer extant because this species may occur opportunistically within its wintering habitat.
The literature available for this species is low to moderate with several general to detailed natural history summaries within the ornithological reference literature. A few controlled scientific studies have been conducted within the physiological ecology literature.
Habitat and Habitat Associations
The California horned lark is a common to abundant resident in a variety of open habitats, usually where trees and large shrubs are absent (Zeiner, et al. 1990). In the Midwest, the species has been characterized as the most abundant species in row-crop fields (Best, et al. 1998). Range-wide, California horned larks breed in level or gently sloping shortgrass prairie, montane meadows, "bald" hills, open coastal plains, fallow grain fields, and alkali flats (Grinnell and Miller 1944). In nonagricultural lands, it typically inhabits areas of short vegetation or bare ground, including shortgrass prairie, deserts, brushy flats, and alpine habitat. In shrubsteppe habitats, it occupies areas characterized by low vegetation. Within southern California, California horned larks breed primarily in open fields, (short) grasslands, and rangelands (Garrett and Dunn 1981; Hamilton and Willick 1996). Grasses, shrubs, forbs, rocks, litter, clods of soil, and other surface irregularities provide cover.
Biogeography
The horned lark has a holarctic distribution, ranging from the Arctic south to central Asia and Mexico with outlying populations in Morocco and Colombia. In general, the northernmost populations are migratory, moving south during the winter into remaining areas of the breeding range. There are also southward movements into areas south of the breeding range, particularly in the southeastern United States (Beason 1995).
The horned lark has increased dramatically in the Midwest and eastern North America from the late 1800s to early 1900s. This expansion has coincided with the deforestation and the creation of agricultural fields and grassland which are good nesting habitat for the horned lark. The species has also shown a southward range expansion between 1900 and 1910 into Kentucky and the Ozark Mountains and then into Oklahoma by the 1920s (Beason 1995).
The California horned lark breeds and resides in the coastal region of California from Sonoma County southeast to the United States/Mexican border, including most of the San Joaquin Valley, and eastward to the foothills of the Sierra Nevada (Grinnell and Miller 1944; AOU 1998). Zeiner, et al. (1990) summarize the distribution, abundance, and seasonality as follows. It is a common to abundant resident in a variety of open habitats, usually where trees and large shrubs are absent. It is found from grasslands along the coast and deserts near sea level to alpine dwarf-shrub habitat above tree line. It is less common in mountain regions, on the north coast (McCaskie, et al. 1979), and in coniferous or chaparral habitats. It mostly leaves the mountains in the winter, but small flocks may remain to winter on windswept, snow-free areas at high elevations in the Sierra Nevada (Gaines 1977). In winter, flocks in desert lowlands and other areas are augmented by winter visitants, many migrating from outside the state (Garrett and Dunn 1981). It is a resident on the Channel Islands (Garrett and Dunn 1981). It is a year-long resident within the state. After breeding, it becomes very gregarious; it often forms large flocks that forage and roost together. Migrants from outside of California join these wintering flocks, especially in the southeastern desert region of the state. Migrant status on the Farallon Islands indicates a latitudinal movement along the coast as well (DeSante and Ainley 1980).
Known Populations Within Western Riverside County
The California horned lark apparently occurs throughout much of western Riverside County in suitable habitat. It is broadly scattered throughout the central portion of the Plan Area. The numbers of horned larks in southern California are greatly augmented in winter by birds from outside the region (Garrett and Dunn 1981). Generally, the species occurs scattered throughout the lower elevations of the MSHCP Plan Area from Prado Basin, south along the Interstate 15 corridor to Temecula, up into the Santa Rosa Plateau, all along the Interstate 215 corridor, the hills and scrub area between the two freeways, then east to the Badlands, south to Vail Lake/Wilson Valley, sparsely in the Badlands and in the Beaumont/ Banning area. It also occurs sparsely within the mountain Bioregions of the Plan Area.
California horned larks are apparently most heavily concentrated in the Prado Basin, Wasson Canyon area, Moreno Valley and March ARB area, Murrieta/ Murrieta Hot Springs area, and Mystic Lake/San Jacinto Wildlife Area (Hays, 1999, pers. obs.; Patten, 1998, pers. comm.). Additional scattered geographic locations recorded within the U.C. Riverside database include: Hemet, Homeland/Lakeview Mountains, Lake Elsinore, Menifee, Rawson Canyon, Reche Canyon, Riverside East, Sage, Temecula/Rancho California, Wildomar, Bautista Creek, San Timoteo Creek, Wilson Creek and Wilson Valley, Diamond Valley Lake, Lake Mathews Reserve, Lake Perris SRA, Lake Skinner, and the Santa Rosa Plateau Nature Reserve.
Biology
Genetics: The horned lark species is divided into 21 subspecies in North America by the fifth American Ornithologists' Union check-list with 15 subspecies in western North America. The subspecies are based primarily on differences in plumage coloration and size, with western populations paler and smaller than eastern and northern populations (Beason 1995).
Diet and Foraging: Horned larks feed primarily on grains and other seeds and shift to mostly insects in the summer months (Bent 1942). It mostly eats insects, snails, and spiders during breeding season; it adds grass and forb seeds and other plant matter to the diet at other seasons (Bent 1942). Individuals forage on the ground in either bare areas or in agricultural fields with short vegetation (Beason 1995). In winter, flocks frequent roadsides, feedlots, and fields where manure from feedlots is spread especially when snow cover is heavy. Sometimes it perches on a plant to take seeds from seed heads. It walks along ground, searching for food. Usually, it is moving while it is feeding but it may also remain in one spot for up to five minutes (Beason 1995). It drinks freely from water holes, but individuals have survived in captivity for 16-31 days without water (Airola 1980).
Daily Activity: In the desert, horned larks may spend much of the day standing in the shade of posts and rocks (Beason 1995).
Reproduction: The horned lark builds a grass-lined nest in a depression on the ground in the open. Individuals are monogamous within a breeding season with no long-term pair bonds formed (Beason 1995). The clutch size varies from two to five eggs (Beason 1995). It breeds from March through July, with a peak in activity in May. The pair nests solitarily. It frequently raises 2 broods in a season (Bent 1942). Incubation is 10-14 days; the altricial young are tended by both parents. The young leave the nest at 9-12 days, and can fly 3-5 days later (Harrison 1978).
Survival: The breeding success rate (fledglings per nest) of the horned lark varies from 23 to 72 percent (Beason 1995).
Dispersal: The young horned larks leave the nest, on average, after ten days (Beason 1995). The dispersal distance is not reported.
Socio-Spatial Behavior: Flock size of horned larks range from 5 to 405 birds per square mile with the variability in flock size dependent on season and local environment (Zeiner et al. 1990). Winter flock size is greatly augmented by winter visitors (Zeiner, et al. 1990). Territory size varies from 0.3 to 5.1 hectares depending on population densities and habitat (Beason 1995). Territories are only maintained during the breeding season and give way to formation of flocks during the winter. Verbeek (1967) estimated a typical territory size as 1.6 hectares (4 acres) in Wyoming alpine tundra. In midwestern farmland, the territory is reported as 0.6 to 3.2 hectares (1.5 to 8 acres) (Beason and Franks 1974), 0.4 to 5.3 hectares (1-13 acres) (Pickwell 1931), and 4.9 hectares (12 acres) (Fitch 1958).
Community Relationships: Eggs and nestlings of the horned lark are subject to predation from mammals and snakes. The adults are prey for falcons. It can be parasitized by brown-headed cowbirds during the second breeding (Beason 1995).
Threats to Species
Continuing threats to the California horned lark include habitat destruction and fragmentation. In nearby Orange County, habitat destruction has significantly reduced the county's nesting and wintering numbers (Hamilton and Willick 1996). The habitat of the California horned lark is easily converted to other landscapes and human uses. Pesticides, specifically Carbofuran and Fenthion, have been shown to poison and kill horned larks (Beason 1995). A total of 44 percent of nest failures have been attributed to mowing in airport grasslands occupied by horned larks (Kershner and Bollinger 1996).
Special Biological Considerations
The Prado Basin population of the California horned lark apparently has remained stable over the course of 14 years of monitoring efforts at that locale (Hays, 1999, pers. obs.).
In the winter, horned larks form large, gregarious, somewhat nomadic groups and may undertake movements to exploit non-uniformly distributed food resources (Beason 1995). Because of the species' use of agricultural fields, the effects of pesticides have been identified as a necessary component of the management of this species (Boutin, et al. 1999). Rangeland alteration activities (removal of shrubs and planting of wheatgrass) in southern Oregon resulted in increased numbers of horned larks after an initial one-year time lag response (Wiens and Rotenberry 1991).
LITERATURE CITED
AOU (American Ornithologists' Union). 1998. Check-List of North American Birds. Seventh Edition. American Ornithologists' Union, Washington, D.C. 829 pp.
Airola, D. A., ed. 1980. California wildlife habitat relationships program: Northeast Interior Zone. Vol III. Birds. U.S. Dep. Agric., For. Serv., Lassen Natl. For., Susanville. 590pp.
Beason, R. C., and E. C. Franks. 1974. Breeding behavior of the horned lark. Auk 91:65-74.
Beason, Robert C. 1995. Horned Lark (Eremophila alpestris) In The Birds of North America, No. 195 (A. Poole and F. Gill, eds.) The Academy of Natural Sciences, Philadelphia, PA and The American Ornithologists' Union, Washington, D.C.
Bent, A. C. 1942. Life histories of North American flycatchers, larks, swallows, and their allies. U.S. Natl. Mus. Bull. 179. 555pp.
Best, L.B., H. Campa, K. E. Kemp, R. J. Robel, M. R. Ryan, J. A. Savidge, S. R. Winterstein, and H. P. Weeks. 1998. Avian abundance in CRP and crop fields during winter in the Midwest. American Midland Naturalist 139:311-314.
Boutin, C., K. E. Freemark, and D. A. Kirk. 1999. Farmland birds in southern Ontario: Field use, activity patterns and vulnerability to pesticide use. Agriculture Ecosystems & Environment 72: 239-254.
DeSante, D. F., and D. G. Ainley. 1980. The avifauna of the South Farallon Islands, California. Studies in Avian Biol. No. 4. Cooper Ornithol. Soc., Lawrence, KA. 104pp.
Fitch, H. S. 1958. Home ranges, territories, and seasonal movements of vertebrates of the Natural History Reservation. Univ. Kans., Lawrence. Publ. Mus. Nat. Hist. 11:63- 326.
Gaines, D. 1977. Birds of the Yosemite Sierra. California Syllabus, Oakland. 153pp.
Garrett, K. and J. Dunn. 1981. Birds of Southern California: Status and Distribution. Los Angeles Audubon Society. 407 pp.
Grinnell, J. and A.H. Miller. 1944. The Distribution of the Birds of California. Pacific Coast Avifauna Number 27. Copper Ornithological Club, Berkeley, California. Reprinted by Artemisia Press, Lee Vining, California; April, 1986. 617 pp.
Hamilton, R. and D.R. Willick. 1996. The Birds of Orange County, California: Status and Distribution. Sea and Sage Press, Irvine, California. 150 pp. with appendices.
Harrison, C. 1978. A field guide to the nests, eggs and nestlings of North American birds. W. Collins Sons and Co., Cleveland, OH. 416pp.
Hays, Loren R. 1999. USFWS, pers. obs.
Kirshner, E.L. and E.K. Bollinger. 1996. Reproductive success of grassland birds at East-central Illinois airports. American Midland Naturalist 136:358-366.
McCaskie, G., P. De Benedictis, R. Erickson, and J. Morlan. 1979. Birds of northern California, an annotated field list. 2nd ed. Golden Gate Audubon Soc., Berkeley. 84pp.
Patten, Michael. 1998. Riverside County Editor for American Field Notes and Past Secretary, California Bird Records Committee, pers. comm.
Pickwell, G. 1931. The prairie horned lark. St. Louis Acad. Sci. Trans. 27:1-153.
Verbeek, N. A. M. 1967. Breeding biology and ecology of the horned lark in alpine tundra. Wilson Bull. 79:208-218.
Wiens, J.A. and J. T. Rotenberry. 1991. Response of breeding passerine birds to rangeland alteration in a North American shrubsteppe locality. Journal of Applied Ecology, v.22, n.3: 655-668.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
California spotted owl (Strix occidentalis occidentalis)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
California spotted owl (Strix occidentalis occidentalis)
Status:
State: Species of Special Concern
Federal: Federal Special Concern species; San Bernardino National Forest Sensitive; Cleveland National Forest Sensitive; Species of Management Concern
GROUP DESIGNATION AND RATIONALE
Group 2
The California spotted owl has a sparse distribution within the Santa Ana Mountains, San Bernardino Mountains and San Jacinto Mountains Bioregions of the MSHCP Plan Area within montane coniferous and oak-deciduous woodlands and forest habitats. It is a Group 2 species because its conservation requires integration of habitat protection with site specific monitoring and management.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 41,370 acres of suitable montane coniferous forest and oak deciduous woodland and forest habitats within the Santa Ana Mountains (7,350 acres), San Bernardino Mountains (1,620 acres), and San Jacinto Mountains (32,400 acres) Bioregions for breeding, foraging, wintering use, and dispersal movement for the California spotted owl.
Objective 2
Include within the MSHCP Conservation Area the nesting locations within the Santa Ana, San Jacinto and San Bernardino mountains.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
Habitat for the California spotted owl includes oak woodland and forest and montane coniferous forest and within canyons in chaparral covered hillsides where oak woodland is present within the Santa Ana Mountains, San Bernardino Mountains, and San Jacinto Mountains bioregions. This provides not only foraging and nesting habitat in the montane areas where the species has been documented to occur, but also provides winter foraging areas for the species if they move to somewhat lower elevations such as to the Santa Rosa Plateau for some period of time. Based on these habitats, the Plan Area supports approximately 57,370 acres of potential habitat for the California spotted owl. Table 1 shows the conservation and loss of potential habitat for the California spotted owl. Overall, approximately 41,370 acres (72 percent) of potential habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public lands.
The California spotted owl occurs within Forest Service lands for nesting within montane coniferous forest and oak woodland and forest habitats. Under the existing Forest Land allocation plan, these locations or habitats are predominantly in the Mt. San Jacinto and Thomas Mountain areas but may also be located within the San Jacinto Wilderness Area as well as the Horse Creek Ridge, Rouse Hill, and Hixon Flat roadless areas in the San Bernardino National Forest, in the Mt. San Jacinto State Park Wilderness (few), and the San Mateo Canyon Wilderness Area (few), Wildhorse and Trabuco roadless areas in the Cleveland National Forest. Within Cleveland National Forest, 90 acres of oak woodland are located within the Tenaja range allotment and 190 acres of oak woodland are located within the Verdugo range allotment. Within the San Bernardino National Forest, 4,090 acres of coniferous and oak woodland are located within the Garner range allotment, 1,140 acres of coniferous and oak woodland are located within the Rouse range allotment and 270 acres of coniferous and oak woodland are located within the Wellman range allotment.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
CALIFORNIA SPOTTED OWL
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| San Bernardino Mountains, San Jacinto Mountains, and Santa Ana Mountains Bioregions | |||||||
| Oak Woodlands and Forests | 27,570 | 1,280 | 19,690 | 20,970 | 4,060 | 2,540 | 6,600 |
| Montane Coniferous Forest | 29,800 | 20 | 20,380 | 20,400 | 40 | 9,360 | 9,400 |
| TOTAL | 57,370 | 1,300 (2%) |
40,070 ( 70% ) |
41,370 (72%) |
4,100 (7%) |
11,900 (21%) |
16,000 (28%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
As described below under Data Characterization, 5 relatively recent (1987 through 1995) point localities have been documented for the MSHCP Plan Area within the UCR database. The 5 point localities are of too low of precision to determine if they are inside the Criteria Area or on Public/Quasi-Public Lands.
Intensive spring surveys for spotted owls were conducted on the San Jacinto Ranger District of the San Bernardino National Forest between 1988 and 1994, for which the results have not been incorporated into the UCR database. Casual surveys have continued since 1994 as opportunity allows. An average of 10 pairs (range 8-14), 6 singles (range 3-9), and 6 juveniles (ranges 1-10) were reported between 1988 and 1994. Areas where owls have been consistently located include: Hall Canyon, North Fork San Jacinto River, Stone Creek, Logan Creek, Pinewood, Fuller Ridge, Dark Canyon, Strawberry Creek, Marion Creek, Hurkey Creek, South Fork San Jacinto River, and Lion Canyon. These areas support predominantly mixed conifer, riparian hardwood and live oak/big-cone Douglas-fir. Other sporadic sightings or vocal detections have occurred on Thomas Mountain and the northeast side of Baldy Mountain. The San Jacinto Wilderness has been largely unsurveyed but few pair may be present. A few, sporadic surveys of Santa Rosa Mountain and Cahuilla Mountain have not yielded any results, although suitable owl habitat does exist (USFS 1999 pers. comm.). The California spotted owl locations are inside the MSHCP Conservation Area within Public/Quasi-Public lands of the San Bernardino National Forest and nest locations will be conserved. Approximately three locations have been recorded in the Cleveland National Forest, however these locations are outside the Plan Area but may use suitable habitat within the Plan Area (Stephenson and Calcarone 1999).
Additional locations of California spotted owls were obtained from the California Department of Fish and Game (Gould 2002 pers. comm.). These locations were generally documented through 1996 but have been updated to include some additional locations through 1998. The CDFG database indicates there are a total of 22 locations within the San Bernardino National Forest, predominantly within the Mt. San Jacinto and Thomas Mountain areas, with one location north of Banning possibly on private land within the San Bernardino National Forest, and two locations within the Santa Ana Mountains within the Cleveland National Forest.
The Forest Service will need to provide protection for specific nesting site locations and potential nesting sites (i.e., large trees) due to their overall sensitivity to disturbance. There are definable locations for focusing conservation efforts within the Forest Service lands within the San Bernardino National Forest and Cleveland National Forest that are composed of conifer forest, oak woodland forest, and may be interspersed with meadows and grasslands. The Forest Service will also need to address fire management within areas occupied by spotted owls as these areas have not burned during recent times. Timber activities will be addressed with respect to the California owl nesting and foraging habitat.
MSHCP Conservation Area Configuration Issues
Known nesting locations, as identified in the previous section, will be conserved as well as habitat potentially supporting the California spotted owl within Criteria Area and Public/Quasi-Public designations, including the montane coniferous and oak woodland habitat within the San Bernardino National Forest, Mt. San Jacinto Wilderness State Park, and Cleveland National Forest. Other areas that are outside of the roadless and wilderness areas may not be so managed. The following large blocks of habitat have not been mapped within the UCR database or by the USFS as containing the California spotted owl: near Santiago Peak in the Cleveland National Forest, Indian Mountain to Poppet Flat, northeastern corner of the Plan Area, area east of Lake Hemet (Spitler Peak and Cone Peak), and Cahuilla Mountain/Red Mountain area. However, these habitat blocks may contain potentially suitable habitat and could be occupied by California spotted owls in the future. As a species with a large foraging area, California spotted owls are likely able to discover and use patches of oak woodland or coniferous habitat that have not been documented to be used in the past. As such, the MSHCP Conservation Area will provide adequate large blocks of habitat as core areas around the currently known nest sites of the species as well as other large blocks of suitable habitat that may be occupied in the future, used for foraging or for wintering.
Rural/Mountainous
As depicted on the MSHCP map (Figure 3-1, MSHCP Volume 1), certain areas adjacent to or in proximity to the MSHCP Conservation Area are designated as Rural/Mountainous in the County's General Plan. A total of 4,100 acres (7 percent) of potential breeding habitat will be designated Rural/Mountainous, which will permit 1 DU/10, 20, or 40 acres depending on slope. These areas are generally constrained for development due to steep topography and the level of development in these areas is anticipated to be of a low density, rural residential character. While these areas will not be included within the MSHCP Conservation Area or managed for the benefit of species conserved under the MSHCP, the low levels of development anticipated in these areas will provide an edge to the MSHCP Conservation Area that may be of value to the California spotted owl.
For the California spotted owl, conservation on the Santa Rosa Plateau may be important for maintaining connection between the Santa Rosa Plateau Nature Reserve and the Santa Ana Mountains. MSHCP Conservation Area locations in these areas are generally surrounded by Rural/ Mountainous designations. Potential development in these areas is anticipated to retain vacant areas that will provide for seasonal movement for this species. No nest sites are located within the Rural/ Mountainous designation.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 41,370 acres of suitable Conserved Habitat and the known nesting localities within large blocks of habitat in the MSHCP Conservation Area.
INCIDENTAL TAKE
Approximately 16,000 acres (about 28 percent) of potential habitat for the California spotted owl will be outside the Criteria Area or Public/Quasi-Public designations, and individuals within these areas will be subject to Incidental Take consistent with the Plan. Approximately five locations from the CDFG database appear to be located outside of the Criteria Area or Public/Quasi-Public designations. Only one of these five locations outside of the MSHCP Conservation Area has been recorded as nesting (1988). No other known nesting areas are outside the Criteria Area or Public/Quasi-Public designations. No take of nesting locations is included within this permit.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS database, the California Natural Diversity Data Base (CNDDB), surveys conducted by the San Bernardino National Forest and a database maintained by the California Department of Fish and Game as well as available literature.
The UCR location database includes five records for the California spotted owl within the Plan Area dated from 1987 to 1995. None of the records is of high precision; one is of moderate precision and recorded for chaparral. The history and status of the records is unknown although the locations are likely extant. One record is within Cleveland National Forest near Highway 74, three records are within the San Bernardino National Forest and one is located in Temecula and is of such low precision that it could be located within the Santa Rosa Plateau. The 1999 USFS census information indicates approximately 10 pairs, 6 singles, and 6 juveniles within the San Bernardino National Forest. The locations for these observations are discussed below. Additional information was obtained from the California Department of Fish and Game from a database that records locations and nesting information of the California spotted owl. This database has been kept up through 1996 with a few additional records added through 1998. A total of 22 locations were provided by CDFG.
The literature available on the California spotted owl, as well as the spotted owl as a whole, is relatively large. It is one of the most-studied and best-known owls in the world. This degree of scientific attention is the result of the owl's association with late seral stage conifer forest of high commercial value. The literature is focused on the natural history of the species, and also includes physiological studies, conservation strategies, and management studies for the species. Several general ornithological reference treatments have been prepared for the species and it has been treated within the general raptor literature. A summary of available information as well as a report of the policy implementation team provides substantial information for the species, only a small part of which is presented within this species account (Standiford et al. 1994). Little information is available with respect to the Plan Area other than general distribution and occurrence information.
Other references that provide information include the Report of the Advisory Panel on the Spotted Owl (Dawson et al. 1986), The Report of the Policy Implementation Planning Team (Standiford et al. 1994), and The California spotted owl: a technical assessment of its current status (Verner et al. 1992).
Habitat and Habitat Associations
In northern California, the northern spotted owl subspecies resides in dense, old-growth, multi-layered mixed conifer, redwood, and Douglas-fir habitats, from sea level up to approximately 2,300 meters (0-7,600 feet). It requires blocks of 40-240 hectares (100-600 acres) of mature forest with permanent water and suitable nesting trees and snags (Forsman 1976). The northern spotted owl was declared Federally Threatened in June 1990.
In southern California, the California spotted owl occurs at lower elevations (sea level to 1,000 meters), and occupies habitats dominated by hardwoods, primarily oak and oak-conifer woodlands (Garrett and Dunn 1981). At higher elevations, up to 2,700 meters (8,500 feet) they inhabit areas dominated by conifers (Gutiérrez et al. 1995; Stephenson 1991). The nesting and roosting habitats are similar to that of the northern spotted owl. The habitats are generally complex in structure with high canopy closure (Gutiérrez et al. 1995). A critical element of this complex forest structure is the presence of large trees greater than 90 centimeters diameter at breast height. In areas where logging has occurred, many large trees are of advanced age, indicating that a residual old growth or late seral stage element is usually present in the breeding and roosting habitat (Gutiérrez et al. 1995). California spotted owls appear to behave as habitat specialists at the scale of nest habitat selection choosing more complex vegetative structure with greater variation in tree sizes, larger trees, and higher canopy closure (LaHaye et al. 1997). In the Sierra Nevada, the owls did not nest where this residual old-growth component was absent. The foraging habitat appears to be more variable and includes both intermediate-aged and older forested habitats within a home range (Gutiérrez et al. 1995). The forests occupied by the California subspecies are less fragmented than random forest areas (Moen 1994). The species uses dense, multi-layered canopy cover for roost seclusion. The habitats selectively chosen by the California spotted owl are live oak/big-cone Douglas-fir forests (41 percent), riparian/hardwood forests (32 percent), and mixed conifer forests (26 percent) (Verner et al. 1992).
Roost selection appears to be related closely to thermoregulatory needs; the species is intolerant of high temperatures (Weathers et al. 2001). It roosts in dense overhead canopy on north-facing slopes in the summer. In winter, it roosts in oak habitats. In northern regions of the state, daytime roosts averaged 165 meters (549 feet) from water; in southern regions, daytime roosts averaged only 51 meters (173 feet) from water (Barrows and Barrows 1978; Barrows 1981).
Biogeography
The spotted owl species as a whole is distributed in western North America and Mexico. It is fairly evenly distributed throughout the northern part of its range but has a more patchy distribution in southern California, southwestern United States, and Mexico. Its breeding distribution is restricted to forest communities. It is found from sea level to as high as 1,200 meters elevation in the northern part of its range and to about 2,700 meters in the southwestern United States (Gutierrez et al. 1995).
California spotted owls are an uncommon, permanent resident that range from the south Cascade Range and northern Sierra Nevada from Pit River, Shasta County, California south through the remainder of the western Sierra Nevada and Tehachapi Mountains to Lebec, Kern County (Zeiner et al. 1990). The California spotted owl is found sparsely east of the Sierra Nevada crest. It occurs in the California coastal ranges from Monterey County south to Santa Barbara County, then in the Transverse Ranges and Peninsular Ranges south to Sierra San Pedro Martir in northern Baja California (Gutierrez et al. 1995). Its distribution is extremely local and fragmentary in southern California and Mexico.
Zeiner et al. (1990) summarize the distribution, abundance, and seasonality of the spotted owl within California as follows: It is an uncommon, permanent resident in suitable habitat within its range as described above. It may move downslope in winter along the eastern and western slopes of the Sierra Nevada, and in other areas within its distribution. The California spotted owl occurs in all of the major mountain ranges in the southern California national forest lands although some ranges support very few pairs (Stephenson and Calcarone 1999). The California spotted owl within southern California is clustered in disjunct mountain and foothill areas where suitable habitat exists and these clusters are generally surrounded by large areas of unsuitable habitat (Stephenson and Calcarone 1999).
A minimum of 3,050 individuals have been detected between 1970 and 1992 within the range of the California spotted owl. A total of 1,008 pairs and 436 single birds are known to occur in the Sierra Nevada and 598 individuals are known from 15 other populations (Gutierrez et al. 1995). The potential population size of the California spotted owl in southern California has been estimated to be potentially 578 pairs (estimated from CDFG database; Standiford et al. 1994). The largest subpopulation of the California spotted owl within the southern California area is the 200-plus territories in the San Bernardino and San Gabriel mountains. Although Cajon Pass separates these two mountain ranges, there is not a major habitat discontinuity and only six miles separate the easternmost San Gabriel territory from the westernmost San Bernardino territory (Stephenson and Calcarone 1999).
Historical distribution is presumed to be the same as the current distribution, although the numbers of individuals may have declined within certain areas and habitats (Gutierrez et al. 1995).
Known Populations Within Western Riverside County
California spotted owls in western Riverside County are found within high-elevation coniferous and hardwood forest areas primarily within Forest Service lands in the San Jacinto Mountains and Palomar Range. It also occurs in the San Bernardino Mountains and the Santa Ana Mountains (Stephenson and Calcarone 1999; Garrett and Dunn 1981).
Low precision geographic locations recorded within the U.C. Riverside database include: Santa Rosa Plateau East, Cleveland National Forest near Highway 74 and San Bernardino Forest near or within the San Jacinto Wilderness area and near Lake Fulmor.
Intensive spring surveys for spotted owls were conducted on the San Jacinto Ranger District between 1988 and 1994. Casual surveys have continued since 1994 as opportunity allows. An average of 10 pairs (range 8-14), 6 singles (range 3-9), and 6 juveniles (ranges 1-10) were reported between 1988 and 1994. Areas where owls have been consistently located include: Hall Canyon, North Fork San Jacinto River, Stone Creek, Logan Creek, Pinewood, Fuller Ridge, Dark Canyon, Strawberry Creek, Marion Creek, Herkey Creek, South Fork San Jacinto River, and Lion Canyon. These areas support predominantly mixed conifer, riparian hardwood and live oak/big-cone Douglas-fir. Other sporadic sightings or vocal detections have occurred on Thomas Mountain and the northeast side of Baldy Mountain. The San Jacinto Wilderness has been largely unsurveyed. A few, sporadic surveys of Santa Rosa Mountain and Cahuilla Mountain have not yielded any results, although suitable owl habitat does exist (USFS pers. comm. 1999).
Biology
Genetics: There are three recognized subspecies: northern spotted owl, California spotted owl, and Mexican spotted owl. The Mexican subspecies is a distinguishable taxon based on allozyme electrophoresis. The analysis of mtDNA sequences shows strong differentiation among currently recognized subspecies, suggesting that the current taxonomy is valid (Gutierrez, et al. 1995).
Diet and Foraging: The spotted owl feeds in forest habitats upon a variety of small mammals, including flying squirrels, woodrats, mice and voles, and a few rabbits. It also eats small birds, bats, and large arthropods. Within the San Bernardino Mountains, the diet of the California spotted owl was summarized as (by frequency of item): Neotoma 39.7 percent, other - primarily invertebrates 38 percent, other mammals 7.3 percent, Peromyscus 7.7 percent, birds 3.5 percent, and Microtus/Clethrionomys 1.7 percent (Gutiérrez, et al. 1995). It usually searches from a perch and swoops or pounces on prey in vegetation or on the ground. It may cache excess food. It forages in late seral stage forests significantly more often than in younger aged stands. Stand attributes include large diameter trees, multiple vegetation strata, and high live-conifer basal area (Gutiérrez, et al. 1995).
Habitat use patterns have been studied for the California spotted owl for the Mt. San Jacinto population (Gutierrez and pritchard 1990). The owls were found primarily in conifer and hardwood stands within conifer forests. A few were observed in live oak forests in deep canyons. The owls were found to not use grasslands, chaparral or open-canopied habitats.
For California spotted owls in the norther Sierra, foraging owls used microhabitats that were characterized by multiple vegetative strata, large tree size classes, high tree basal areas and woody debris. The mean home range for foraging birds within this area has been determined to be 1,439 hectares (Call et al. 1992).
Daily Activity: The California spotted owl exhibits year-long, nocturnal activity (Forsman 1976).
Reproduction: The spotted owl usually nests in a tree or snag cavity or in a broken top of a large tree. It may also nest in a large mistletoe clump, abandoned raptor or raven nest, cave or crevice, on a cliff or on the ground (Zeiner, et al. 1990, Call 1978). Mature, multi-layered forest stands are required for breeding of the spotted owl (Remsen 1978). The nest is usually placed 9-55 meters (30-180 feet) above the ground. The spotted owl breeds from early March through June, with a peak in April and May. It has one brood per year. The clutch size is 1-4 eggs, usually 2. The female incubates and broods the young; the male feeds the female and the young. It may not be sexually mature until 3 years old. The pair may use the same breeding site for 5-10 years, but may not breed every year (Forsman 1976).
The quality of nesting habitat and nest-site selection of a population of the California spotted owl in the San Bernardino Mountains was studied by LaHaye et al. (1997). This study concluded that fledging success was unrelated to nest type, nest tree, nest stand characteristics, or habitat type. Nest productivity was greatest in lower elevation oak/big-cone Douglas-fir habitat and was quantified as 1.7 fledglings per successful nest. Nest stands were characterized by greater variation in tree size, higher canopy closure, and greater basal area of large trees compared with random points. This confirms that the California spotted owls will use a variety of habitats but these habitats are consistently characterized by greater structural complexity compared with available habitat.
Survival: The juvenile survival rate is low and adult survival rate is relatively high for the California spotted owl (LaHaye, et al. 1992). There is empirical evidence from the San Bernardino Mountains that spotted owl reproductive success is significantly higher in lower montane canyon live oak/big-cone Douglas-fir forests than it is in high-elevation montane conifer forests (La Haye et al. 1997). These lower elevation habitats are believed to be productive because of high woodrat densities (the owl's primary prey) in the surrounding chaparral (Stephenson and Calcarone 1999).
Dispersal: California spotted owls are known to migrate altitudinally due to heavy snow pack (Zeiner, et al. 1990). Juveniles disperse from the natal areas in September and October; the species has a strong fidelity to the nest site (Gutiérrez, et al. 1995). Dispersal studies of the California spotted owl population in the San Bernardino Mountains concluded theat juvenile owls dispersed 0.4 to 36.4 kilometers (LaHaye et al. 2001)
Socio-Spatial Behavior: Forsman et al. (1977) found home ranges of the spotted owl in mature Douglas-fir/hemlock forests in Oregon of 120-240 hectares (300-600 acres), with a mean of 180 hectares (450 acres). Gould reported a similar home range size in the Sierra Nevada (Gould 1974). Individual sites are spaced 1.6 to 3.2 kilometers (1-2 miles) apart in suitable habitat (Marshall 1942, Gould 1974). Gould (1977) found that the territory in conifer forests in the Sierra Nevada varied from 40-138 hectares (100-340 acres), with a mean of 93 hectares (230 acres). In the San Bernardino Mountains, home ranges for three California spotted owls were 804 acres, 2,232 acres and 4,611 acres (Gutierrez and LaHaye 1988).
Community Relationships: Great horned owls and goshawks are potential predators of the young spotted owls (Forsman 1976). The spotted owl will actively defend the nest site from common ravens, northern goshawks, and Cooper's hawks. It will attack great horned owls. Researchers may be attacked when attempting to get near the nest (Gutierrez et al. 1995).
Threats to Species
The loss of habitat owing to clear felling of forests, and degradation of habitat owing to even-aged tree management are the primary threats to the California spotted owl. Extensive loss of habitat in all three subspecies' ranges has occurred. Secondary losses of habitat include urban and suburban expansion, water development in riparian corridors, agricultural development, fuel wood/oak harvest, reservoir development and mining (Gutiérrez, et al. 1995). The USFS (pers. comm. 1999) identified a major threat to the species as the loss of habitat by wildfire. Much of the forest area has not burned since the advent of fire suppression at the turn of the century.
Cases of shooting or trapping owls have been documented and sometimes the spotted owl is killed by automobiles. The extent of mortality from these causes is unknown but is expected to be low (Gutierrez et al. 1995).
Special Biological Considerations
Two populations in southern California have shown declining trends within the last decade. Little is known about the mechanisms limiting and regulating the population size; however nest sites and prey availability may serve as limiting factors (Gutierrez et al. 1995). California spotted owls are believed to function as a metapopulation with separate subpopulations connected by infrequent but persistent interchange of individual owls (Stephenson and Calcarone 1999; Verner et al. 1992; LaHaye et al. 1994).
About one-quarter to one-third of California spotted owls are known to migrate altitudinally due to heavy snow pack in the Sierra Nevada. That is, in the winter, when territories at higher elevations become covered with snow, the owls will move to lower elevations, comprised primarily of hardwoods, in order to hunt (Forsman 1976). The California spotted owl in the San Gabriel Mountains have often been located at the lower elevations at the base of the mountains during annual Christmas bird counts (Verner et al. 1992).
The species requires blocks of 100 to 600 acres of mature forest with permanent water and suitable nesting trees and snags (Forsman 1976). The California spotted owl requires mature forest stands with large trees and snags (Gutiérrez, et al. 1995).
Evidence exists that forests selectively logged in the past can be re-occupied by owls relatively soon (40 to 100 years) if residual forest elements (e.g., snags, coarse woody debris, large trees with cavities) are present (Gutiérrez, et al. 1995).
The California spotted owl on Mt. San Jacinto appears to be well distributed above 1,000 meters in forested habitats (Gutierrez and Pritchard 1990). Densities in the area have been estimated at 0.16 owls per square kilometer. The proportion of subadults in this isolated population is over twice that reported for large contiguous populations of spotted owls which suggests a higher adult mortality. The fecundity on the insular population is either lower than or similar to the northern spotted owl.
For the California spotted owl, a team of scientists and wildlife managers was assembled to conduct a technical assessment of the California subspecies (Standiford et al. 1994; Verner et al. 1992). This team devised an interim conservation plan that specifically recommended protecting all known owl nesting areas, key habitat elements (e.g., large trees), and logging strategies that retained large trees in the Sierra Nevada. The current owl protection plan in southern California includes the protection of all known owl sites on federal forest land.
LITERATURE CITED
Barrows, C. W. 1981. Roost selection by spotted owls: an adaptation to heat stress. Condor 83:302-309.
Barrows, C. W., and K. Barrows. 1978. Roost characteristics and behavioral thermoregulation in the spotted owl. Western Birds 9:1-8.
Call, M.W. 1978. Nesting habits and survey techniques for common western raptors. U.S. Dept. Interior Bureau of Land Management. Portland Oregon. Technical Note No 316. 115 pp.
Call, D. R., R. J. Gutierrez, and J. Verner. 1992. Foraging habitat and home-range characteristics of California spotted owls in the Sierra Nevada. Condor 94:880-888.
Dawson, W. R, D. E. S. Brown, J. D. Ligon, J. R. Murphy, J. P. Myers, D. Simberloff, and J. Verner. 1986. Report of the Advisory Panel on the spotted owl. Audubon Conservation Report No. 7. National Audubon Society, New York.
Forsman, E. D. 1976. A preliminary investigation of the spotted owl in Oregon. M.S. Thesis, Oregon State Univ., Corvallis. 127 pp.
Forsman, E. D., E. C. Meslow, and M. J. Strub. 1977. Spotted owl abundance in young versus old-growth forests. Oregon. Wildl. Soc. Bull. 5:43-47.
Garrett, K. and J. Dunn. 1981. Birds of Southern California: Status and Distribution. Los Angeles Audubon Society. 407 pp.
Gould, G. I., Jr. 1974. The status of the spotted owl in California. Calif. Dep. Fish and Game, Sacramento, Admin. Rep. No. 74-6. 36 pp.
Gould, G. I., Jr. 1977. Distribution of the spotted owl in California. West. Birds 8:131-146.
Gould G. I., Jr. 2002. California Department of Fish and Game. pers. comm.
Gutierrez, R. J., and J. Pritchard. 1990. Distribution, density, and age structure of spotted owls on two southern California habitat islands. Condor 92:491-495.
Gutiérrez, RJ, A.B. Franklin, and W. S. LaHaye. 1995. Spotted owl (Strix occidentalis). In: A. Poole and F. Gill, Eds. The birds of North America. Number 179.
Gutierrez, Rocky J., and W. S. LaHaye. 1988. Ecology of the California spotted owl in the San Bernardino Mountains of California. Progress Report No. 3. Submitted to the San Bernardino National Forest and Snow Summit Ski Corporation. Humboldt State University Foundation.
LaHaye, W. S., R. J. Gutierrez, and D. R. Call. 1992. Demography of an insular population of spotted owls (Strix occidentalis occidentalis). In Wildlife 2001: populations (D. R. McCullough and R. H. Barrett, eds.). Elsevier Applied Science.
LaHaye, W. S., R. J. Gutierrez, and H. R. Akcakaya. 1994. Spotted owl metapopulation dynamics in southern California. Journal of Animal Ecology 63: 775-785.
LaHaye, W. S., R. J. Gutierrez, and D. R. Call. 1997. Nest-site selection and reproductive success of California spotted owls. Wilson Bulletin 109:42-51.
LaHaye, W. S., R. J. Gutierrez, and J. R. Dunk. 2001. Natal dispersal of the spotted owl in southern California: dispersal profile of an insular population. Condor 103: 691-700.
Marshall, J. T., Jr. 1942. Food and habitat of the spotted owl. Condor 44:66-67.
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coastal California gnatcatcher (Polioptila californica californica)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
coastal California gnatcatcher (Polioptila californica californica)
Status:
State: Species of Special Concern (full species)
Federal: Threatened
GROUP DESIGNATION AND RATIONALE
Group 2
The coastal California gnatcatcher is distributed widely within suitable habitat in the Riverside lowlands and San Jacinto Foothills Bioregions especially along the Interstate 15/215 corridor from the Santa Ana River to Temecula and into the Vail Lake area. It is absent from the higher elevations and desert areas. The Coastal California gnatcatcher occurs in 16 Core Areas within the Plan Area including Alessandro Hills, El Cerrito, Lake Mathews-Estelle Mountain Reserve, Alberhill area, the proposed North Peak Conservation Bank/Meadowbrook area, Wasson Canyon, Railroad Canyon, Quail Valley, Sedco Hills, Hogbacks, Murrieta Hot Springs, Lake Skinner, Buck Road to Pourroy Road east of Murrieta Hot Springs, Vail Lake/Wilson Valley including the eastern Temecula Creek area, Rancho California east of Interstate 15 to De Portola Road, and Norco Hills. The coastal California gnatcatcher, as a year-round resident, has lower dispersal capabilities than small passerine birds that are long-distance migrants and thus relies on habitat linkages for localized and regional movements. Because the coastal California gnatcatcher is well known for using coastal sage scrub within the lowland and foothill Bioregions, occurs widely within its suitable habitat, but has specific locations that are Core Areas, it is included as a group 2 species to be managed at a habitat level with site specific requirements in Core Areas and linkages.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information existing at the time of MSHCP preparation. Pursuant to the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives may be adjusted as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 77,070 acres of suitable habitat including coastal sage scrub, Riversidean alluvial fan scrub and desert scrub in the Riverside Lowland and San Jacinto Foothills Bioregions.
Objective 2
Include within the MSHCP Conservation Area at least 13 of the Core Areas and interconnecting linkages within 9 Core and Linkage areas including El Cerrito/Lake Mathews-Estelle Mountain Reserve (Existing Core C plus Proposed Extension of Existing Core 2; 23,710 acres), Alberhill area (Subunit 2 of the Elsinore Area Plan; 3,460 acres), the proposed North Peak Conservation Bank/Meadowbrook area (Subunit 6 of the Elsinore Area Plan; 1,080 acres), Wasson Canyon (Subunit 5 of the Elsinore Area Plan; 2,320 acres), Railroad Canyon/Sedco Hills (Proposed Linkage 8; 5,470 acres), a portion of the Quail Valley area (Proposed Linkage 7; 3,400 acres), Hogbacks/Murrieta Hot Springs (Proposed Core 2 plus Existing Constrained Linkage A; 5,350 acres), Lake Skinner/Buck Road to Pourroy Road east of Murrieta Hot Springs (Existing Core J plus Proposed Extension of Existing Core 5, 6, and 7; 29,060 acres), Vail Lake/Wilson Valley including the eastern Temecula Creek area (Proposed Core 7; 50,000 acres). Due to mapping configuration, some of the coastal California gnatcatcher Core Areas have been combined in order to provide the acreage of MSHCP Conservation Area within the Core Area.
Objective 3
Within the MSHCP Conservation Area, maintain (once every three years) continued use of and successful reproduction at 75 percent of the Core Areas. Successful reproduction is defined as a nest which fledged at least one known young.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
The primary habitat for the coastal California gnatcatcher includes coastal sage scrub, desert scrubs, and Riversidean alluvial fan scrub within the Riverside lowlands and San Jacinto foothills Bioregions. Frequently, pockets of coastal sage are located within a matrix of chaparral or grassland areas and these pockets may be occupied. In addition, gnatcatchers occupy other secondary habitats (i.e., chaparral, grasslands, riparian). These secondary habitats may be important as nesting, foraging, and/or dispersal areas, however, only a small proportion of these habitats are occupied and, therefore, only primary habitat is used for the purpose of the conservation analysis (although some unquantified additional conservation value will be provided by the conservation of secondary habitats within the Core Areas and linkages within the MSHCP Conservation Area). The Plan Area supports approximately 140,770 acres of primary habitat for the coastal California gnatcatcher. Table 1 shows the conservation and loss of primary habitat for the coastal California gnatcatcher. A total of 77,070 acres (55 percent) of the primary habitats, coastal sage scrub, desert scrubs, and Riversidean alluvial fan scrub habitats, are conserved within Criteria Area and Public/Quasi-Public Lands.
As part of 1995 PSBS/KTU+A work referenced in the discussion of MSHCP vegetation (MSHCP Chapter 2), PSBS and KTU+A modeled and evaluated variables potentially relevant to the suitability of coastal sage scrub habitat within the Plan Area for the coastal California gnatcatcher. A detailed description of the methodology used to develop the model is presented in their report (PSBS and KTU+A, 1995). The 1995 PSBS/KTU+A work was designed to gather and organize existing information on current and future land uses, identify gaps of information, and evelope tools to evaluate potential alternative reserve designs focused on doastal sage scrub and coastal California gnatcatchers. Variables considered included elevation, slope, patch size, patch shape, proximity to other coastal sage scrub patches, isolation of patches and adjacent land use. The modeling results labeled areas as very high, high, moderate, low and very low with respect to the quality of coastal sage scrub. A total of 104,820 acres of moderate, high, and very high quality coastal sage scrub habitat (PSBS and KTU+A 1995) is present within the Plan Area. These three categories of the habitat quality mapping overlap with the all of the Core Areas of the coastal California gnatcatcher. The high and very high quality coastal sage scrub categories overlap with all of the core population areas except for that in the Hogbacks and Rancho California areas and portions of the Murrieta Hot Springs and Buck Road to Pourroy Road east of Murrieta Hot Springs areas. A total of 64,010 acres (61 percent) of moderate, high and very high quality of coastal sage scrub habitat (based on mapping in PSBS and KTU+A 1995) is conserved within Criteria Area or Public/Quasi-Public Lands. This includes 14,460 acres (80 percent) of the very high quality habitat, 30,700 acres (58 percent) of the high quality habitat, and 16,350 acres (48 percent) of the moderate quality habitat.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
COASTAL CALIFORNIA GNATCATCHER
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| Riverside Lowlands and San Jacinto Foothills Bioregions | |||||||
| Desert Scrubs | 2,230 | 2,160 | 0 | 2,160 | 40 | 30 | 70 |
| Riversidean Alluvial Fan Sage Scrub | 5,430 | 2,710 | 1,310 | 4,020 | 160 | 1,250 | 1,410 |
| Coastal Sage Scrub | 133,110 | 43,690 | 27,200 | 70,890 | 19,740 | 42,480 | 62,220 |
| TOTAL | 140,770 | 48,560 (34%) |
28,510 (20%) |
77,070 (55%) |
19,940 (14%) |
43,760 (31%) |
63,700 (45%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
As described below under Data Characterization, 391 of the 521 point localities within the UCR database have a high location precision. Of these 391 point localities, 234 (60 percent) will be inside the Criteria Area or Public/Quasi-Public Lands. A total of 27 (7 percent) will be in the Rural/Mountainous zone. However, of the 130 (33 percent) points located outside these habitat areas, 37 are mapped in existing residential/urban/exotic areas.
As indicated above, there are definable locations for focusing conservation efforts (i.e., Core Areas for the coastal California gnatcatcher and the linkage areas between the cores). These areas include El Cerrito, Lake Mathews-Estelle Mountain Reserve, Alberhill area, the proposed North Peak Conservation Bank/Meadowbrook area, Wasson Canyon, Railroad Canyon area, a portion of the Quail Valley area, Sedco Hills, Hogbacks, Murrieta Hot Springs, Buck Road to Pourroy Road east of Murrieta Hot Springs, Lake Skinner, and Vail Lake/Wilson Valley including the eastern Temecula Creek area. These Core Areas have been combined in some cases and are reflected by the acreage calculated for each core as follows: El Cerrito/Lake Mathews-Estelle Mountain Reserve (Existing Core C plus Proposed Extension of Existing Core 2; 23,710 acres), Alberhill area (Subunit 2 of the Elsinore Area Plan; 3,460 acres), the proposed North Peak Conservation Bank/Meadowbrook area (Subunit 6 of the Elsinore Area Plan; 1,080 acres), Wasson Canyon (Subunit 5 of the Elsinore Area Plan; 2,320 acres), Railroad Canyon/Sedco Hills (Proposed Linkage 8; 5,470 acres), a portion of the Quail Valley area (Proposed Linkage 7; 3,400 acres), Hogbacks/Murrieta Hot Springs (Proposed Core 2 plus Existing Constrained Linkage A; 5,350 acres), Lake Skinner/Buck Road to Pourroy Road east of Murrieta Hot Springs (Existing Core J plus Proposed Extension of Existing Core 5, 6, and 7; 29,060 acres), Vail Lake/Wilson Valley including the eastern Temecula Creek area (Proposed Core 7; 50,000 acres). The total Core Area acreage conserved within the MSHCP Conservation Area is 123,850 acres. The three core population areas not proposed for conservation (Alessandro Hills, Norco Hills, and Rancho California east of Interstate 15 to De Portola Road) within the MSHCP Conservation Area are generally located within very constrained areas that have already been highly developed. These areas consist of fragmented, small patches of coastal sage scrub habitat. The patches have very high edge effects and some of the point locations have been lost to development.
MSHCP Conservation Area Configuration Issues
Several large blocks of habitat supporting the coastal California gnatcatcher will be conserved as Criteria Area and Public/Quasi-Public Lands including the Core Areas at El Cerrito, Lake Mathews-Estelle Mountain Reserve, Alberhill area, the proposed North Peak Conservation Bank/ Meadowbrook area, Wasson Canyon, Railroad Canyon, a portion of the Quail Valley area, Sedco Hills (relatively low number of gnatcatchers but important for the reserve configuration), Hogbacks, Murrieta Hot Springs, Lake Skinner, Buck Road to Pourroy Road east of Murrieta Hot Springs, and Vail Lake/Wilson Valley including the eastern Temecula Creek area. Other locations occupied by the coastal California gnatcatcher but not constituting a Core Area that will be conserved include Sycamore Canyon Regional Park, portions of Temecula west of Interstate 15, and the Badlands.
Areas that are important for preservation for dispersal purposes but that may not contain large numbers of gnatcatchers include several areas that provide essential connections outside of the Plan Area to other populations of the coastal California gnatcatcher. Conservation of areas within the Jurupa Mountains, Pigeon Pass Road area, San Timoteo Creek and the Badlands provide connectivity into San Bernardino County. Conservation of areas in the Cleveland National Forest near the 91 Freeway and Chino Hills area provide connectivity into Orange County. Conservation within the Santa Rosa Plateau Nature Reserve, Santa Margarita Ecological Reserve, and Aguanga area provide connection into San Diego County.
Within the Plan Area there are also large areas conserved that may provide dispersal corridors but that do not contain large number of gnatcatchers. Conservation of the foothills of the Santa Ana Mountains within Cleveland National Forest is provided west of Interstate 15 which provides a broad area for dispersal on the west side of Interstate 15. Conservation of riparian habitat from the Prado Basin along the Santa Ana River provides a linkage that may not be used consistently but that is composed of habitat that the coastal California gnatcatcher has been documented to use occasionally and could use for dispersal.
Conservation of both Core Areas in the form of large blocks of habitat, as described above, as well as narrower linkages for movements between the core population areas is essential for the MSHCP Conservation Area configuration and conservation strategy. Although the gnatcatcher is not as adept at dispersing as some of the long distance migrant bird species, it has been documented to disperse at least 1.1 kilometers (Galvin 1998). Based on observations of coastal California gnatcatchers in a variety of natural and non-natural habitats, it is expected that they may disperse across marginal habitats such as agriculture, disturbed habitats (e.g., fallow fields, abandoned vineyards) and non-native grasslands and are capable of moving across roadways. As much as possible, it is recommended that linkages be as wide as a gnatcatcher territory within the Western Riverside County area, which has been estimated at approximately 400 meters (approximately 1,200 feet), feet based on the diameter of an average territory. Generally, in order to protect against adverse edge effects, it is better for the linkage to be wider than 400 meters (approximately 1,200 feet), however, some areas are currently constrained and for short distances, narrow linkages or stepping stone reserves will be required.
As such, the MSHCP Conservation Area will provide adequate habitat linkages between Core Areas for this species. Linkage widths in the Home Gardens area south to the El Cerrito Core Area are approximately 0.8 to 1.2 kilometers wide. The El Cerrito, Lake Mathews-Estelle Mountain Reserve, and Alberhill Core Areas are contained within a large block of contiguous habitat that at its narrowest is approximately 1.7 kilometers in width. The connection between the Alberhill Core Area and the North Peak Conservation Bank/Meadowbrook area is a narrow (approximately 0.4 kilometers) but relatively short constrained connection of approximately 2 kilometers in length. At that, the linkage is still the minimum width of a territory diameter. The connection between the North Peak conservation Bank Core Area and the Wasson Canyon Core Area also is narrow but also is very short (0.4 kilometer for 0.8 kilometer). The portion of the Quail Valley Core Area that is conserved is well connected to the Wasson Canyon area with the conservation in BLM parcels and Kabian Park. Similar to the North Peak connection to Wasson Canyon, the Wasson Canyon Core Area has a narrow but short linkage to the Railroad Canyon Core Area. This linkage is approximately 0.3 kilometer wide for approximately 0.5 kilometer in length. The Sedco Hills Core Area is a long habitat patch that varies in width from 0.8 kilometer to 1.7 kilometers in width with one pinch point of approximately 0.4 kilometer.
The Sedco Hills Core Area is separated from the Hogbacks area by Interstate 215, however a narrow linkage is provided via a drainage approximately half-way between Scott Road and Clinton Keith Road. This linkage is approximately 0.4 kilometer wide for approximately 0.8 kilometer. The Hogbacks Core Area is a large habitat block that is connected to the Lake Skinner large habitat block and the Buck Road to Pourroy Road large habitat block by narrow linkages that are currently constrained by existing development. These linkages are located within drainages and are provided as more than one linkage to provide for duplicity of connections. These linkages are within the Warm Springs drainage, Tucalota Creek, and Santa Gertrudis Creek. The Lake Skinner Core Area is linked to the Vail Lake/Wilson Valley including the eastern Temecula Creek Core Area by preservation east of Lake Skinner along Tucalota Creek in a 0.8 to 1.25 kilometer linkage. A very large block of habitat is conserved in the Vail Lake/Wilson Valley including the eastern Temecula Creek area which adjoins the San Bernardino National Forest to the east and to the Cleveland National Forest to the south.
Stepping stone reserves conserve some locations of gnatcatchers and connect some of the smaller numbers of Coastal California gnatcatchers which do not comprise core populations including: Sycamore Canyon Regional Park which is connected by Box Springs Mountains to Highgrove by either very narrow drainages or stepping stone reserve and also is connected by stepping stone reserves through the Alessandro Hills and Mockingbird Canyon through wetlands preservation to El Cerrito.
The conservation strategy and MSHCP Conservation Area design for the gnatcatcher takes into account that large scale fires damage gnatcatcher habitat for a relatively long length of time and large areas are necessary to provide refugia for birds and to supply dispersing individuals to a recovered area for re-population. Within the Plan Area, the Alberhill Core Area is separated from other Core Areas by an existing firebreak in the form of the I-15 freeway corridor. Thus, if a wildfire occurs east or west of I-15, the population on the opposite side of the freeway will likely be protected. Duplicate linkages also provide for the temporary loss of function of the coastal sage scrub habitat in the event of a fire (Campbell et al. 1998). A duplicity of habitat linkages composed of sage scrub and other undeveloped habitats which may be composed of native as well as non-native habitats may provide for dispersal ability of the species (Campbell et al. 1998). Several duplicate linkages are preserved within the MSHCP Conservation Area. Between the Hogbacks and Core Areas at Lake Skinner and AD161 area, a network of linkages is designed. Several linkages occur between the Core Areas on the east side of Interstate 15 and the west side to the Cleveland National Forest at Indian Canyon and Horsethief Canyon.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 77,070 acres of suitable Conserved Habitat and 13 Core Areas within large blocks of habitat in the MSHCP Conservation Area. In addition, implementation of Objective 3 for this species will document that the MSHCP Conservation Area will maintain (once every three years) the continued use of and successful reproduction at 75 percent of the Core Areas. Successful reproduction is defined as a nest which fledged at least one known young.
The current number of locations of the gnatcatcher in Riverside County is estimated at 250 to 300 pairs. The gnatcatcher is restricted to more lowland areas and is not distributed evenly through the preferred habitat. It occurs in a patchy distribution and thus the suitable habitat as well as the Core Areas and connections of these Core Areas need to be addressed as described in detail above. Numerous small patches and small numbers of gnatcatchers are conserved as well and are likely to be important as providing a source of dispersing birds. These small populations, many of which are documented above to be preserved may be important to prevent further isolation of remaining breeding groups.
INCIDENTAL TAKE
About 63,700 acres of potential primary habitat for the coastal California gnatcatcher will be outside the Criteria Area and Public/Quasi-Public designations, or about 45 percent of the total potential primary habitat. Of this, approximately 19,940 acres (14 percent) of potential primary habitat is located within Rural/Mountainous designation areas. Based on the evaluation of habitat quality provided by PSBS and KTU+A (1995), approximately 40,810 acres (39 percent) of moderate, high and very high quality habitat will be outside the MSHCP Conservation Area. This includes 3,470 acres (19 percent) of the very high quality habitat, 20,680 acres (39 percent) of the high quality habitat, and 16,660 acres (49 percent) of the moderate quality habitat.
Core areas not conserved within Criteria Area and Public/Quasi-Public designations include the Norco Hills population (approximately 5 locations), Alessandro Hills (approximately eight locations), a portion of the Quail Valley area (approximately six locations), and Rancho California east of Interstate 15 to De Portola Road (approximately 10 locations some of which may no longer be extant due to recent development in the area). Based on the UCR database, a total of 27 locations (7 percent) will be in the Rural/Mountainous zone and 130 locations (33 percent) are located outside the MSCHP Conservation Area. However, of the 130 points, 37 are mapped in existing residential/ urban/exotic areas.
SPECIES ACCOUNT
Data Characterization
The location database for the coastal California gnatcatcher contains approximately 521 data points which range in the date of the location point from 1888 to 1999. Approximately 391 data records are of a high degree of precision and will be useful for analysis although many of these point locations could represent duplicate counts for areas that were surveyed in the early 1990s and then surveyed again. The database indicates that there is an adequate amount of information regarding the overall population size and that patterns of occurrences represent areas of use. The habitats represented in these recent and high precision records include coastal sage scrub, chaparral, grassland, alluvial fan scrub, residential or developed, reservoir, agriculture land, and two within riparian or oak woodland habitat. Approximately324 of the recent data records are of a high precision, currently located within Riversidean sage scrub/grassland/chaparral habitats from the vegetation overlay for the Plan Area. Thus, these points are likely to be extant. Approximately 50 of the more recent (1990 or later) and high precision location code data points are overlain with residential/urban/exotic vegetation types and likely no longer exist.
Due to the recent listing and various federal actions regarding the coastal California gnatcatcher and the location within a rapidly developing area of the United States, as well as the controversy that has surrounded the listing of the species, the coastal California gnatcatcher has been well studied by the scientific community and the available literature on the species is very large ( USFWS 1991; USFWS 1993; USFWS 1995; USFWS 1996; USFWS 1999; USFWS 2000) . The literature includes studies on the natural history, habitat requirements, management implications and recommendations. The gnatcatcher has been well studied in western Riverside county mainly due to the establishment of the Southwestern Riverside County Multiple Species Reserve and the accompanying management fund. In addition there is an excellent baseline for the distribution of the gnatcatcher populations within the Plan Area boundary.
Habitat and Habitat Associations
The coastal California gnatcatcher (gnatcatcher), a subspecies of the California gnatcatcher, is a small member of the thrush family (Muscicapidae). The gnatcatcher typically occurs in or near sage scrub habitat, which is a broad category of vegetation that includes the following plant communities as classified by Holland (1986): Venturan coastal sage scrub, Diegan coastal sage scrub, maritime succulent scrub, Riversidean sage scrub, Riversidean alluvial fan sage scrub, southern coastal bluff scrub, and coastal sage-chaparral scrub. Coastal sage scrub is composed of relatively low-growing, dry-season deciduous, and succulent plants. Characteristic plants of this community include California sagebrush (Artemisia californica), various species of sage (Salvia sp.), California buckwheat (Eriogonum fasciculatum), lemonadeberry (Rhus integrifolia), California encelia (Encelia californica), and Opuntia spp. Ninety-nine percent of all gnatcatcher locality records occur at or below an elevation of 984 feet (Atwood 1990).
Coastal sage scrub is patchily distributed throughout the range of the gnatcatcher, and the gnatcatcher is not uniformly distributed within the structurally and floristically variable coastal sage scrub community. Rather, the subspecies tends to occur most frequently within the California sagebrush-dominated stands on mesas, gently sloping areas, and along the lower slopes of the coast ranges (Atwood 1990). An analysis of the percent gap in shrub canopy supports the general impression that gnatcatchers prefer relatively open stands of coastal sage scrub (Bontrager 1991). The gnatcatcher occurs in high frequencies and densities in scrub with an open or broken canopy while it is absent from scrub dominated by tall shrubs and occurs in low frequencies and densities in low scrub with a closed canopy (Weaver 1998). The territory size increases as vegetation density decreases and with distance from the coast, probably due to food resource availability. Thus, gnatcatchers will use even sparsely vegetated coastal sage scrub for shelter and to forage for insects as long as perennial shrubs are available (ERCE 1990).
Gnatcatchers also use chaparral, grassland, and riparian or alluvial habitats where they occur adjacent to sage scrub (Bontrager 1991). The use of these habitats appears to be most frequent during late summer, autumn, and winter, with smaller numbers of birds using such areas during the breeding season. These non-sage scrub habitats are used for dispersal, but data on dispersal use are largely anecdotal (Bowler 1995; Campbell et al. 1995). Although existing quantitative data may reveal relatively little about gnatcatcher use of these other habitats, these areas may be critical during certain times of the year for dispersal or as foraging areas during drought conditions (Campbell et al. 1998). Breeding territories have also been documented in non-sage scrub habitat. Campbell et al. (1998) discuss likely hypotheses explaining why non-CSS habitat is used by gnatcatchers including food source availability, dispersal areas for juveniles, temperature extremes, fire avoidance, and lowered predation rate for fledglings.
Environmental, vegetational, and food-abundance characteristics are important aspects of territory quality, however, they are related to the time of year when the evaluation is made (Redak et al. 1997). Based on the studies of Redak et al. (1997) during the breeding season, habitat use was negatively associated with distance to the coast and the elevation of the territory. The habitat use was positively associated with the abundance of adult stages of beetles, flies, spiders and larval stages of all arthropods. Plots with high densities of California sagebrush, flat-topped buckwheat, and white sage were also used by birds. In contrast, during the nonbreeding season, the correlation of habitat use with vegetation and location variables remained but the correlation was no longer present with the arthropod communities.
Biogeography
Historically, gnatcatchers occurred from southern Ventura County southward through Los Angeles, Orange, Riverside, San Bernardino, and San Diego counties, and into Baja California, Mexico, to approximately 30 degrees north latitude near El Rosario (Atwood 1990). A detailed analysis of elevational limits associated with gnatcatcher locality records reveals that a significant portion, 65 to 70 percent of the historic range, may have been located in southern California rather than Baja California (USFWS 2000). The gnatcatcher was considered locally common in the mid-1940's, but by the 1960's this subspecies had declined substantially in the United States owing to widespread destruction of its habitat (Atwood 1990). Currently, the subspecies occurs on coastal slopes of southern California, ranging from southern Ventura southward through Palos Verdes Peninsula in Los Angeles County through Orange, Riverside, San Bernardino and San Diego Counties into Baja California to El Rosario, Mexico, at about 30 degrees north latitude (Atwood 1991). In 1993, the USFWS estimated that approximately 2,562 pairs of gnatcatchers remained in the United States. Of these, 30 pairs occurred in Los Angeles County, 757 pairs occurred in Orange County, 261 pairs occurred in Riverside County, and 1,514 pairs occurred in San Diego County.
Known Populations Within Western Riverside County
The gnatcatcher is found throughout lowland and foothill Bioregions of western Riverside county in coastal sage scrub habitat. The high density areas are found in the western portion of the county along the I-15 corridor continuing east within the southern portion of the Plan Area to Lake Skinner and Vail Lake. The distribution of gnatcatchers in the County does not appear to be uniform along this strip, instead high density patches of several Core Areas exist in generally two locations within the Plan Area, one in the northwestern portion of the Plan Area east of Interstate 15 between Lake Mathews and the City of Lake Elsinore. The other area is in the Murrieta Hot Springs/Lake Skinner area and west to Interstate 215. In 1993, the USFWS estimated the number of pairs of gnatcatchers at 261 (USFWS 1993). Current estimates for gnatcatchers in western Riverside County number around 300 pairs, however the confidence intervals were not reported (USFWS 1996).
From north to south, Core Areas occur at Norco Hills, Alessandro Hills, El Cerrito, Lake Mathews-Estelle Mountain Reserve, Alberhill area, the proposed North Peak Conservation Bank/ Meadowbrook area, Wasson Canyon, Railroad Canyon, Quail Valley, Sedco Hills, Hogbacks, Murrieta Hot Springs, Lake Skinner, Buck Road to Pourroy Road east of Murrieta Hot Springs, Vail Lake/Wilson Valley and eastern Temecula Creek area, and Rancho California east of Interstate 15 to De Portola Road. Other locations with a few gnatcatcher locations but not a key population include Sycamore Canyon Regional Park, Mockingbird Canyon, Temecula west of Interstate 15, and the Badlands.
Biology
Genetics: The coastal California gnatcatcher was originally described as a distinct species by Brewster (1881) based on specimens, however, Grinnell (1926) concluded that it is a subspecies of the black-tailed gnatcatcher (Polioptila melanura) which is widely distributed throughout the Sonoran and Chihuahuan deserts of the southwestern United States and Mexico. Atwood (1980, 1988) concluded that the species was specifically distinct from P. melanura, based on differences in ecology and behavior, which was adopted by the American Ornithologists' Union Committee on Classification and Nomenclature (American Ornithologists Union 1957, 1989). Recent mitochondrial DNA sequencing confirmed the species-level recognition of the Coastal California gnatcatcher, which was calculated to differ from the black-tailed gnatcatcher (P. melanura) by 4.0 percent, similar to differences calculated in the black-capped gnatcatcher (P. nigriceps) and white-lored gnatcatcher (P. albiloris) (Zink and Blackwell 1998).
Diet and Foraging: The coastal California gnatcatcher is primarily insectivorous, nonmigratory, and exhibits strong site tenacity (Atwood 1990). The diet deduced from fecal samples resulted in leaf- and plant hoppers and spiders predominating the samples. True bugs, wasps, bees, and ants were only minor components of the diet (Burger et al. 1999). Gnatcatcher adults selected prey to feed their young that was larger than expected given the distribution of arthropod size available in their environment, and chicks were provisioned with larger prey items and significantly more grasshoppers and crickets and spiders. Both adults and young consumed more sessile than active prey items (Burger et al. 1999).
The richness of the insect community within a habitat area may be a useful tool for describing the quality of the habitat (Burger et al. 1996). This is especially important for strictly insectivorous species such as the coastal California gnatcatcher. Gnatcatcher habitat use has been positively associated with total insect species richness and total individual insect abundance (Redak et al. 1996). Thus overall food abundance and diversity plays an important role in territory selection and use for this species (Redak et al. 1996). Habitat use during the non-breeding season showed no clear relationship to any component of the arthropod community (Redak et al. 1997).
Daily Activity: Activity budget data indicate that gnatcatchers are most active and vocal during the morning. A lull in activity usually occurs during mid-day and activity increases again late in the day (Mock et al., 1990).
Reproduction: The breeding season of the gnatcatcher extends from mid February through mid-August, with the peak of nesting activity occurring from mid-March through mid-May. The gnatcatcher nest is a small, cup-shaped basket usually found one to three feet above the ground in a small shrub or cactus. Clutch sizes range between three and five eggs, with the average being four. Juvenile birds associate with their parents for several weeks (sometimes months) after fledging (Atwood 1990). The coastal California gnatcatcher is a year-round resident. Nest building begins during the mid part of March with the earliest recorded egg date approximately March 20 (Mock et al., 1990). Post-breeding dispersal of fledglings occurs between late May and late November. Predation may be a major source of nest failure (Bontrager 1991; Grishaver et al. 1998). In western Riverside County, 78.9 percent of the nesting attempts failed with 52.9 percent suffering from nest predation (Braden 1999).
Nest site attendance by male gnatcatchers was determined to be equal to that of females for the first nest attempt and then decline to almost 1/3 of that of the female for later nesting attempts (Sockman 1998).
The frequency with which various plant species have been recorded as nesting substrata indicates the overall preference of the sage scrub community as the habitat type (Atwood 1980). California sagebrush was chosen 25 percent of the time with other species including white sage, black sage, chamise, cholla, buckthorn, orange, lemonadeberry, and others making up the balance of nest shrub selections (Atwood 1980).
Survival: Gnatcatchers are persistent nest builders and often attempt multiple broods typically upon nesting failure, which is suggestive of a high reproductive potential. This is, however, typically offset by high rates of nest predation and brood parasitism (Atwood 1990). High rates of nest failure may account for the high number of nesting attempts of the coastal California gnatcatcher (Grishaver et al 1998). Gnatcatchers typically live for two to three years, although ages of up to five years have been recorded for some banded birds (Braden et al. 1995). Most of the juvenile birds usually die during the cold winter months, although the percentage was not quantified. Observations indicate that gnatcatchers are highly vulnerable to extreme cold, wet weather (Mock et al., 1990).
Dispersal: Dispersal is a means by which genetic and demographic exchange between subpopulations maintains the viability of the regional metapopulation (Bailey and Mock 1998). Details regarding the dispersal effect on genetic and demographic connectivity of subpopulations and the actual requirements for dispersal are largely unknown (Rotenberry and Scott 1998) but some information can be documented from anecdotal observations. The mean dispersal distance of gnatcatchers banded as nestlings for males was 2.85 km and for females was 3.33 km (Atwood et al. 1996). Mean dispersal of juveniles in Orange County was found to be 1.05 km with one individual dispersing a total of 7.55 km (Galvin 1998). Although the mean dispersal distances that have been documented above are relatively low, dispersal of juveniles is difficult to observe and to document without extensive banding studies. It is likely that the few current studies underestimate the gnatcatcher's typical dispersal capacity because of the difficulty of detecting (Bailey and Mock 1998). Juvenile coastal California gnatcatchers are apparently able to traverse highly man-modified landscapes, including non-native landscaping vegetation, for at least short distances and this underestimation of the species' dispersal capability can lead to an overestimation of the metapopulation's vulnerability to extinction (Bailey and Mock 1998). A few observations of gnatcatcher dispersal behavior indicate that a stepping stone linkage, that is, a serious of small patches of suitable habitat interspersed with developed habitat, is deemed acceptable for situations where the habitat is otherwise fragmented and no contiguous linkage is available (Bailey and Mock, 1998). Additionally, natural and restored coastal sage scrub habitat along highway corridors has been documented to be used for foraging and nesting by gnatcatchers and may serve important dispersal functions (Famolaro and Newman 1998). Typically, however, the dispersal of juveniles requires a corridor of native vegetation which provides foraging and cover opportunities to link larger patches of appropriate sage scrub vegetation (Soule 1991). These dispersal corridors may facilitate the exchange of genetic material and provide a path for recolonization of areas from which the species has been extirpated and increased mating opportunities for unpaired birds (Soule 1991; Galvin 1998).
The natal dispersal, for a non-migratory bird, such as the coastal California gnatcatcher, is an important aspect of the biology of the species (Galvin 1998).
Socio-Spatial Behavior: The coastal California gnatcatcher seems to become highly territorial by late February or early March each year. Males seem to be very vocal during this time period (Mock et al., 1990). In San Diego County the territory size for inland sites was calculated to range between 13 and 39 acres per pair, averaging 24 acres per pair (ERCE 1990). In Riverside County, it was estimated that about 24 acres of sage scrub habitat (3 times the average territory size of 8 acres as measured within the HCP area) was required per pair of coastal California gnatcatchers (Braden 1998, pers. comm.). The distribution of the gnatcatcher is thought to be related to elevation with most of the birds located below 250 m elevation within 35 km of the coast and 500m elevation for inland regions (Atwood and Bolsinger 1992). During the nonbreeding season, gnatcatchers have been observed to wander in adjacent territories and unoccupied habitat increasing their home range size to approximately 78 percent larger than their breeding territory (Preston et al. 1998). Estimates of the territory size should be examined with caution as the calculation may be influenced by differences in data collection and analysis (Atwood et al. 1998).
Coastal California gnatcatchers are most often observed in pairs even in the non-breeding season. They appear to maintain their territories and are relatively sedentary throughout the year (Dunn and Garrett 1987). In fact vocalization rates, which may provide communication within the pair, were highest from August through March (Preston et al. 1998).
Community Relationships: Predation occurs in greater proportion in the upper and lower one third of the nest shrub. Predation was lower in nests with full clutch sizes which may indicate the parents are more attentive to the nest after the clutch is complete (Sockman 1997). Potential predators include scrub jays, greater roadrunners, and cactus wrens which have been observed to be actively mobbed by the gnatcatcher (Bontrager 1991). The coastal California gnatcatcher also is known to be affected by nest parasitism of the brown-headed cowbird. However, the gains in nest success from decreased nest parasitism appear to be negated by increased nest abandonment due to predation before cowbirds have migrated into an area (Braden et al. 1997). Thus, although a cowbird trapping program may reduce parasitism significantly and lower abandonment due to parasitism, nest predation then increases and negates the benefit of the trapping program (Braden et al. 1997). Nest parasitism apparently has resulted in earlier nesting dates of the gnatcatcher which may help compensate for the negative affect of parasitism (Patten and Campbell 1998).
Although the coastal California gnatcatcher may serve as an adequate "umbrella species" for other species that occur in similar habitats and that require a similar territory size or smaller (Fleury et al. 1998), it is not a particularly good indicator of bird-species richness in coastal sage scrub habitat (Chase et al. 1998).
Threats to Species
In 1997, the total number of gnatcatchers in the United States was estimated at 2,899 pairs, after subtracting out all gnatcatcher pairs authorized for Take under Habitat Loss Permits, approved natural Community Conservation Plans, Habitat Conservation Plans, and section 7 consultations ("Reinitiation of formal consultation on implementation of the special rule for the coastal Coastal California gnatcatcher [1-6-93-FW-37R1]"). This apparent increase in abundance since 1993 is likely the result of additional surveys occurring within previously unsurveyed areas, as well as increased productivity in response to favorable climatic conditions (USFWS 2000).
Although observed declines in numbers and distribution of the gnatcatcher resulted from numerous factors, habitat destruction, fragmentation and adverse modification are the principal reasons for the gnatcatcher's current threatened status (USFWS 1993). The amount of coastal sage scrub available to gnatcatchers has continued to decrease during the period after the listing of the species. It is estimated that up to 90 percent of coastal sage scrub vegetation has been lost as a result of development and land conversion (Westman 1981a, 1981b; Barbour and Major 1977), and coastal sage scrub is considered to be one of the most depleted habitat types in the United States (Kirkpatrick and Hutchinson 1977; Axelrod 1978; Klopatek et al. 1979, Westman 1987; O'Leary 1990). The fragmentation of habitat may artificially increase populations in adjacent preserved habitat; however, these population surpluses may be lost in subsequent years due to crowding and lack of resources (Scott 1993). In addition, agricultural use, such as grazing and field crops, urbanization, air pollution, increases in fire frequency and the introduction of exotics have all had an adverse impact on extant sage scrub habitat. A consequence of urbanization that is contributing to the loss, degradation, and fragmentation of coastal sage scrub is an increase in wildfires due to anthropogenic ignitions (human caused fires). High fire frequencies and the lag period associated with recovery of the vegetation may significantly reduce the viability of affected subpopulations of the gnatcatcher (USFWS 1991).
Special Biological Considerations
Knowledge of the demography of a population is fundamental to determining long-term trends. For birds, the demographic parameters of primary importance are annual breeding success, defined as number of chicks fledged per pair, and recruitment, defined as percentage of fledglings that enter the breeding population. A preliminary demographic model for a population of coastal California gnatcatchers based on observed data was prepared by Woehler et al (1995). Based on the results, for the population to be stable, each breeding pair must replace themselves over their lifetime. The data from a population at U.C. Irvine had a 90 percent mortality (that is, a 10 percent recruitment) and produced 0.64 fledglings per egg. In western Riverside County, 78.9 percent of the nesting attempts failed which translates to an approximately 80 percent mortality (Braden 1999). Thus, for the U.C Irvine example, a pair must produce 30 eggs during their lifetime and must live for five years for the population to remain stable (Woehler et al. 1995).
Gnatcatcher populations appear to be inversely correlated to seasonal total rainfall (Erickson and Miner 1998). Thus increased rainfall during the winter is a mixed blessing in that it is likely that it increases winter mortality but may increase the productivity of the invertebrate prey population base (Erickson and Miner 1998). Other weather-related factors that may influence the distribution of the gnatcatcher include the January mean minimum temperature which, for the coastal California gnatcatcher, has been estimated to be approximately 2.5 degrees C (Mock 1998). This metabolic constraint may preclude gnatcatchers, as a sedentary bird, from occupying otherwise suitable habitat within their range (Mock 1998). This link between a species distribution and physiological adaptations to the climate has been shown previously for other bird species (Hayworth and Weathers 1984).
Gnatcatchers nested earlier, had more successful nests, produced more fledglings, had a longer nesting period, and had lower fledgling costs when their territories were associated with increased grass and forb cover, increased perennial structure, increased horizontal perennial homogeneity, decreased vertical perennial homogeneity, and decreased perennial diversity (Braden et al. 1997). Thus, assessment of habitat quality should take into account these variables for preserve planning.
A habitat-based metapopulation model developed for the coastal California gnatcatcher revealed that the model predicted a fast decline and high risk of population extinction with most combinations of population parameters. The results were most sensitive to density-dependent effects, the probability of weather-related catastrophes, adult survival, and adult fecundity (Akcakaya and Atwood 1997). However, this metapopulation model resulted in the greatest difference on a time horizon of only a few decades. This may be appropriate if the model is used to compare alternative management options but not to make assessments with longer time horizons (Akcakaya and Atwood 1997). Studies providing information on long-scale demography and metapopulation variables are still largely unknown (Rotenberry and Scott 1998).
Structure of the perennial vegetation within coastal sage scrub seems to be an important component leading to successful gnatcatcher reproduction (Braden, 1997). Any disturbance that affects perennial structure and homogeneity within gnatcatcher territories, such as fire or grazing, also may affect gnatcatcher fitness (Braden, 1997). In fact, areas of the Southwestern Multiple Species Reserve that were occupied by gnatcatchers previous to a 1993 fire have not recovered enough to warrant occupation by gnatcatchers to date (Shaughnessy 1999 pers. comm.). In general, recently burned areas are not used by gnatcatchers except on an occasional basis, and five to seven years of recovery may be necessary before gnatcatchers will nest in burned areas (Atwood et al. 1998, Beyers et al. 1994). This slow recovery of CSS in western Riverside county may be due to invasion of exotic annuals after any disturbance. CSS in the County has been reduced by frequent fire, grazing, and invasion of exotic annuals, as well as air pollution (O'Leary and Westman 1988; O'Leary (1990). The frequency of fires in wildland areas tends to increase as fragmentation increases due to urbanization and agricultural activity. Because of the CSS to grass conversion, protection of coastal sage scrub on gabbro basalts may be required to protect this habitat and the gnatcatcher in Riverside County (Minnich and Dezzani 1998).
Fire may be an important factor to consider in MSHCP Conservation Area design for this species and management plans may be necessary to provide a strategic framework for merging the needs for the species with the challenges of fire control (Mackey et al. 1994). Consideration of habitat refugia, burn frequency, and recolonization of recovering burn areas will be necessary for designing reserves for this species (Atwood, et al. 1998). Observations after a major fire of coastal sage scrub reveal that a large proportion of the gnatcatchers within the burned area were displaced to adjacent habitat rather than killed outright and were packed more densely into remaining areas of intact coastal sage scrub (Atwood, et al. 1998). On unburned areas within San Diego and Riverside counties, two pairs per hectare were found, but only 0.02 pair per hectare were found on burned areas (Mayer and Wirtz 1995). However, the gnatcatchers that are able to establish territories on burned areas appear to breed at rates very similar to those on unburned sites (Wirtz and Mayer 1995). The extent and timing of vegetation recovery may determine the habitat suitability for breeding pairs (Wirtz and Mayer 1995).
The presence of gnatcatchers within burned areas may indicate post-fire dispersal or the availability of refugia from the fire (Mayer and Wirtz 1995). Frequent burning of coastal sage scrub may lead to domination of the site by introduced grasses, in addition, burned sage scrub often remains unsuitable for breeding gnatcatchers for more than eight years after burning (ERCE 1991, Zedler et al. 1983, O'Leary 1990). At an inland site, burned 12 years earlier, there was less than 10 percent shrub cover and no gnatcatchers, while annual grasses and mustard species dominated the site (Beyers et al. 1994). Management consideration will need to take into account that large scale fires may damage gnatcatcher populations in both the burned area and the refugia area (Atwood et al. 1998). Due to the issue of periodic fires in occupied habitat and the length of time needed for recovery of CSS, large areas will be necessary to provide refugia for birds and to supply dispersing individuals to a recovered area. As an example within the western Riverside County Plan Area, the Alberhill population is separated from other core populations by an existing firebreak in the form of the I-15 freeway corridor. Thus, if a wildfire occurs east or west of I-15, the population on the opposite side of the freeway will likely be protected. Duplicate linkages also provide for the temporary loss of function of the coastal sage scrub habitat in the event of a fire (Campbell et al. 1998). A duplicity of habitat linkages composed of sage scrub and other undeveloped habitats which may be composed of native as well as non-native habitats may provide for dispersal ability of the species (Campbell et al. 1998).
Other factors that will be relevant for designing a reserve system for the gnatcatcher will be the dispersal distance and average territory size. In western Riverside County, the average dispersal distance for juvenile gnatcatchers has been documented as 1.14 km (Braden et al., 1994a). The distances may be influenced by many factors such as sex, reproductive opportunities, available habitat and other factors. The average territory size for gnatcatchers is 8.42 acres during the breeding season and can expand to 60 acres during the non-breeding season (Braden and Powell, 1994b). Other studies have concluded the territory ranges in size depending on the location and a study in Riverside County concluded the average territory size is 8 acres (ERCE 1990, Braden 1998, pers. comm.). A reserve design for this species will need to maintain connections of breeding habitat such that dispersal between areas can be accomplished and that are large enough to accommodate the largest territory sizes.
Linkages of habitat along linear features such as highways and power-line corridors may be of significant value in linking populations of the gnatcatcher (Famolaro and Newman 1998). Stepping stone linkages which are designed to function as habitat linkages are acceptable but should be line of sight as much as possible (Bailey and Mock 1998). The width of a linkage is recommended to be approximately 1,200 feet. This will provide a linkage wide enough to support a gnatcatcher territory. For linkages less than this width, the gnatcatchers currently mapped for occurring within the linkage may not be able to remain within the area. In the case of narrow habitat widths, the linkage will serve the function of connection of habitat areas only. An important linkage of habitat to maintain or encourage is that from the western Riverside County area north into San Bernardino County (Davis et al. 1998). This linkage is within the Jurupa Hills and connects to the Santa Ana River in Riverside County (Davis et al. 1998). Recently, gnatcatchers have been observed within Jurupa Hills although the area is not surveyed regularly (Davis et al. 1998).
The coastal California gnatcatcher may be suitably analyzed on a landscape or habitat basis rather than on a data point basis due to the fact that it responds well to habitat management and will readily occupy revegetated coastal sage scrub (O'Connell and Erickson 1998, Miner et al. 1998). The fact that gnatcatchers will occupy revegetated coastal sage scrub makes this an important component of long-term management for the species (O'Connell and Erickson 1998). In one study, restored habitat was included in 19 of 22 gnatcatcher territories and nests in restored areas were as likely to produce at least one young as nests in naturally generated scrub (Miner et al. 1998). Additionally, in this study, thirteen percent of the nests were placed within 3 meters of actively used roads or trails and their success rate was similar to that of nests placed further from these high-use areas, thus breeding success of gnatcatchers appears not to be negatively affected by current management practices and levels of public use within park areas. (Miner et al. 1998). Given that this study was conducted within specific State Park areas, additional studies would be helpful for other situations.
The continued fragmentation of habitat over time has increased exposure of gnatcatcher to threats associated with habitat edge (Atwood 1993). Numerous nest predators thrive on habitat edges, and brood parasitism by the brown-headed cowbird (Molothrus ater) appears to be exacerbated by increased edge effects (Bolger et al. 1997, Atwood 1993). Management of edge effects of future development may also be needed although there is little evidence that coastal California gnatcatchers are negatively affected by having their territory located at the edge of urban development (Atwood, 1998). This may be more associated with the use of the gnatcatcher of sage scrub/grassland ecotone. In support of this observation, studies of ‟edge/fragmentation reduced" species versus ‟edge/ fragmentation enhanced" species places the coastal California gnatcatcher in an ‟edge/fragmentation insensitive" category (Bolger et al. 1997). This is a category occupied by the characteristic species of shrub habitats in the region. They tend to be abundant and widely distributed across the landscape and habitat gradients although their abundance is much lower than the other species in the group (Bolger et al. 1997). Other forms of edge management may still be required. Management may include fencing areas occupied by gnatcatchers to protect birds from human and other intruders. Management may include exotic plant removal along edges of development or planting with native shrubs. Analysis of the current shrub cover to shrub cover and composition in 1934 indicates a drastic reduction in native species and increase in non-native grasses and forbs (Minnich and Dezzani 1998). A major portion of the degradation in the Perris plain of Riverside County is within public land with private lands nearby containing higher quality habitat. Attempts to conserve the coastal California gnatcatcher by extending public lands in regions experiencing this habitat degradation may be insufficient (Minnich and Dezzani 1998).
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Cooper's hawk (Accipiter cooperii)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
Cooper's hawk (Accipiter cooperii)
Status:
State: Species of Special Concern
Federal: Partners in Flight Priority Bird Species; San Bernardino National Forest Sensitive
Other: Audubon Society Blue List
GROUP DESIGNATION AND RATIONALE
Group 2
The Cooper's hawk is widely distributed throughout the MSHCP Plan Area within suitable habitat. It occurs within all Bioregions of the Plan Area. There are several areas that appear to be Core Areas including the Prado Basin/Santa Ana River, San Timoteo Canyon, Temescal Wash, Wasson Canyon, Slater Canyon, Santa Rosa Plateau West, Temecula Creek, Murrieta Creek, Tucalota Creek, Vail Lake, Wilson Valley, San Bernardino National Forest, and Cleveland National Forest. Because it is well known for using riparian scrub, forest and woodland, oak woodland and forest, and montane coniferous forest, occurs in all Bioregions of the Plan Area, but has specific locations that are Core Areas, it is a Group 2 species.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 54,580 acres of suitable habitat including riparian scrub, forest, and woodland, oak woodland and forest, and montane coniferous forest.
Objective 2
Include within the MSHCP Conservation Area at least 10 Core Areas at (1) the Prado Basin/Santa Ana River (9,670 acres), (2) San Timoteo Canyon (Subunit 3 of The Pass Area Plan; 2,290 acres), (3) Temescal Wash (Subunit 3 of Temescal Canyon Area Plan; 4,010 acres), (4) Wasson Canyon (Subunit 5 of Elsinore Area Plan; 2,320 acres), (5) Temecula Creek (Subunit 2 of Southwest Area Plan; 850 acres), (6) Murrieta Creek (Subunit 1 of Southwest Area Plan; 2,060 acres), (7) Vail Lake (Subunit 3 of Southwest Area Plan; 12,320 acres), (8) Wilson Valley (Subunit 2 of REMAP Area Plan; 33,540), (9) San Bernardino National Forest (Existing Core K;149,750 acres), (10) Cleveland National Forest (Existing Core B; 71,490 acres).
SPECIES CONSERVATION ANALYSIS
Conservation Levels
For the purpose of the conservation analysis, potential habitat for the Cooper's hawk includes riparian scrub, woodland, and forest habitat, oak woodland and forest, and montane coniferous forest within all Bioregions of the Plan Area. Based on these habitats, the Plan Area supports approximately 76,680 acres of potential habitat for the Cooper's hawk. Table 1 shows the conservation and loss of potential habitat for the Cooper's hawk. Overall, approximately 54,580 acres (71 percent) of potential habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public Lands.
This species occurs within the Forest Service lands as well as the lowland Bioregions as a breeding and foraging species. It occurs predominantly within riparian scrub, woodland and forest, oak woodland and forest, and montane coniferous forest. Under the existing Forest Land allocation plan, these locations and habitats are generally located within the San Jacinto Wilderness and San Mateo Canyon Wilderness areas and in most of the grazing allotments as well. The Cooper's hawk has been documented to occur in the area of Fulmor Lake and Pine Cove and along the foothills areas and within the western portion of the Cleveland National Forest. Conservation of riparian and woodland habitats and Core Areas within the San Bernardino National Forest and Cleveland National Forest are important conservation methods for this species.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
COOPER'S HAWK
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| All Bioregions | |||||||
| Riparian Scrub, Woodland, Forest | 14,610 | 3,920 | 7,270 | 11,190 | 370 | 3,050 | 3,420 |
| Woodlands and Forests (oak) | 32,180 | 2,390 | 20,500 | 22,890 | 5,020 | 4,270 | 9,290 |
| Montane Coniferous Forest | 29,890 | 20 | 20,480 | 20,500 | 40 | 9,350 | 9,390 |
| TOTAL | 76,680 | 6,330 (8%) |
48,250 (63%) |
54,580 (71%) |
5,430 (7%) |
16,670 (22%) |
22,100 (29%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
As described below under Data Characterization, 85 of the 178 relatively recent point localities have a precision of "1." Of these 85 point localities, 16 (19 percent) will be inside the Criteria Area and 14 (17 percent) are located within Public/Quasi-Public Lands. A total of 12 (14 percent) will be in the Rural/Mountainous lands. Of the 43 high precision recent points located outside the MSHCP Conservation Area, 21 points are located in residential/urban/exotic or agriculture areas and may have been observed in flight. One of these 43 locations outside the MSHCP Conservation Area was observed within suitable habitat composed of riparian habitat and the balance are located outside suitable habitat areas within non-native grassland, chaparral, or Riversidean sage scrub. Conservation of this species will be considered from a landscape perspective due to the fact that the suitable habitat has been well defined. Providing additional suitable habitat that is not currently occupied may assist with the recovery of the species.
In addition, there are definable locations composed of Core Areas for focusing conservation efforts which are included within the MSHCP Conservation Area. These conserved Core Areas include the Prado Basin/Santa Ana River (9,670 acres), San Timoteo Canyon (Subunit 3 of The Pass Area Plan; 2,290 acres), Temescal Wash (Subunit 3 of Temescal Canyon Area Plan; 4,010 acres), Wasson Canyon (Subunit 5 of Elsinore Area Plan; 2,320 acres), Temecula Creek (Subunit 2 of Southwest Area Plan; 850 acres), Murrieta Creek (Subunit 1 of Southwest Area Plan; 2,060 acres), Vail Lake (Subunit 3 of Southwest Area Plan; 12,320 acres), Wilson Valley (Subunit 2 of REMAP Area Plan; 33,540). The Core Areas within the San Bernardino National Forest (Existing Core K;149,750 acres) and Cleveland National Forest (Existing Core B; 71,490 acres) are conserved as described above. A total of 288,300 acres of Core Areas as estimated by the subunit acreages (core acreage for the forest service lands) are conserved within the MSHCP Conservation Area. Constrained areas of Tucalota Creek and a portion of Santa Rosa Plateau West are conserved.
Rural/Mountainous Designation Areas
As depicted on the MSHCP Plan Map (Figure 3-1, MSHCP Volume I), certain areas adjacent to or in proximity to the MSHCP Conservation Area are designated as Rural/Mountainous in the County's General Plan. These areas are generally constrained for development due to steep topography and the level of development in these areas is anticipated to be of a low density, rural residential character. While these areas will not be included within the MSHCP Conservation Area or managed for the benefit of species conserved under the MSHCP, the low levels of development anticipated in these areas will provide an edge to the MSHCP Conservation Area that may be of value to certain species. For the Cooper's hawk, conservation of the Santa Rosa Plateau along the Tenaja Corridor and Slater Canyon just west of Lake Elsinore are important as a core population areas. MSHCP Conservation Area locations in these areas are generally surrounded by Rural/Mountainous designations. Potential development in these areas is anticipated to retain vacant areas, and wetlands in particular due to the Riparian/Riverine Areas and Vernal Pools policy, which will provide nesting and foraging habitat for the Cooper's hawk. A total of 5,430 acres (7 percent) of potential habitat will be designated Rural/Mountainous.
MSHCP Conservation Area Configuration Issues
Several large blocks of habitat supporting or potentially supporting the Cooper's hawk will be conserved as Criteria Area and Public/Quasi-Public designations, including the Prado Basin/Santa Ana River, Sycamore Canyon Regional Park, Lake Mathews-Estelle Mountain, Wasson Canyon, Sedco Hills, foothills of the Santa Ana Mountains, Cleveland National Forest, a portion of the Santa Rosa Plateau, Lake Skinner-Diamond Valley Lake, San Jacinto Wildlife Area-Lake Perris, the Badlands, Vail Lake, Wilson Valley, San Jacinto River, Lake Elsinore, Badlands and Potrero Valley. Some of these areas include Core Areas. Other drainages that are provided protection by the designation as MSHCP Conservation Area, including areas occupied by Cooper's hawk or containing Core Areas of the Cooper's hawk, include Temescal Wash, San Timoteo Creek, Temecula Creek, Tucalota Creek, Bautista Creek, and Murrieta Creek. Protection is also provided within Cleveland National Forest and San Bernardino National Forest areas as discussed above. Some of the large blocks of habitat have not been mapped as containing Cooper's hawks or drainages with riparian or woodland habitat. However, these habitat blocks may have smaller riparian systems that contain potentially suitable habitat and could be occupied by Cooper's hawks in the future. As a long-distance migrant and a species with a large foraging area, Cooper's hawks are likely able to discover and use patches of riparian or woodland habitat that have not been documented to be used in the past. As documented below, the Cooper's hawk is willing to nest within relatively close contact to humans and may even occur within suburban areas as a nesting bird.
Additionally, the MSHCP Conservation Area will provide adequate habitat linkages or stepping stones between Core Areas for this species and will include smaller drainages that may support small numbers of the species. The Prado Basin Core Area is linked along the Santa Ana River to San Bernardino and Orange counties. This riparian area is linked to the south by the Temescal Wash to Lake Mathews and Lake Elsinore. Riparian habitat within the Vail Lake area is linked to the Lake Skinner-Diamond Valley Lake area via Rawson Canyon. Tucalota Creek provides a linkage from Lake Skinner to Murrieta Creek. The Vail Lake area is also linked to the Santa Rosa Plateau and then to the Santa Margarita River by the riparian habitat in Temecula Creek and Murrieta Creek. The Badlands area provides a major habitat block that provides a linkage to Potrero Creek, Lake Perris and Mystic Lake/San Jacinto Wildlife Area, and to San Timoteo Creek.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 54,580 acres of suitable Conserved Habitat and 10 Core Areas including the Prado Basin/Santa Ana River, San Timoteo Canyon, Temescal Wash, Wasson Canyon, Temecula Creek, Murrieta Creek, Vail Lake, Wilson Valley, San Bernardino National Forest, and Cleveland National Forest.
INCIDENTAL TAKE
About 22,100 acres (29 percent) of potential habitat for the Cooper's hawk will be outside the Criteria Area and Public/Quasi-Public designations and individuals within these areas will be subject to Incidental Take consistent with the Plan. Of this, approximately 5,430 acres (7 percent) of potential habitat are located within Rural/Mountainous designation areas. While the Rural/ Mountainous areas are not included within the MSHCP Conservation Area and will not be managed for the benefit of wildlife, the anticipated levels of development in these areas will likely be consistent with maintaining some habitat for the Cooper's hawk. A portion of the core population within the Santa Rosa Plateau is within the Rural/Mountainous designation and is not considered to be conserved. The population at Slater Canyon is also within the Rural/Mountainous designation and is not considered to be conserved. The core population area at Tucalota Creek is constrained by existing development and although habitat is provided within the drainage by conserved riparian scrub, woodland and forest, the individuals within this drainage are not considered to be conserved.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The location database for the Cooper's hawk includes approximately 230 data records from 1888 to 2000. Of these records, approximately 178 are relatively recent (within the past 10 years) and of these, 85 are of high precision and may be accurately located within the Plan Area. Approximately 21 of these high precision records are located within developed areas and although they may no longer exist, they may represent a wintering or transient bird hunting within a residential neighborhood. The rest occur within non-native grassland, sage scrub, chaparral, riparian and oak woodlands, montane coniferous, open water/reservoirs, crop lands and other vegetation communities that are likely occupied by the species for foraging or nesting. The database does not identify those records that are breeding locations.
A moderate amount of literature is available for the Cooper's hawk because it is a bird of prey and is of interest from a community perspective in relation to potential competition with congeners. Most of the literature pertains to general natural history, niche determination, and the accipiters in general. Few controlled scientific studies have been conducted. However, some management studies are available. Very little information is available for the Plan Area other than what is available regarding basic distribution information.
Habitat and Habitat Associations
Throughout its range, the Cooper's hawk breeds in deciduous, mixed, and evergreen forests and deciduous stands of riparian habitat (Rosenfield and Bielefeldt 1993). The Cooper's hawk breeds primarily in riparian areas and oak woodlands and apparently is most common in montane canyons (Garrett and Dunn 1981; Hamilton and Willick 1996). It frequents landscapes where wooded areas occur in patches and groves and it often uses patchy woodlands and edges with snags for perching (Beebe 1974). This species is seldom found in areas without dense tree stands or patchy woodland habitat (Zeiner, et al. 1990). Within the range in California, it most frequently uses dense stands of live oak, riparian deciduous, or other forest habitats near water (Zeiner, et al. 1990). Dense stands with moderate crown-depths are usually used for nesting (Zeiner, et al. 1990). The Cooper's hawk tends to nest in stands with lower densities of taller and larger trees and a greater proportion of hardwood cover than conifer species when compared to other accipiters (Trexel, et al. 1999). Migrant and wintering birds are generally more catholic in their choice of habitats and may be found with regularity in developed (e.g., suburban) areas. They hunt in broken woodland and habitat edges, catching predominantly avian prey in the air, on the ground, and in vegetation.
The Cooper's hawk apparently reduces the niche overlap with the northern goshawk by using areas with greater shrub cover, flatter terrain, and locations that are closer to roads, forest openings, and human habitation (Bosakowski, et al. 1992).
The Cooper's hawk is tolerant of human disturbance and habitat fragmentation and breeds in suburban and urban settings (Murphy, et al. 1988). The urban sites have included isolated trees in residential neighborhoods with commercial and recreational activities less than 150 meters distant and houses 20 to 30 meters distant. Typically, there is some forest edge habitat included within their home range even if nesting within an urban setting and this forest edge may serve as the primary hunting site (Rosenfield and Bielefeldt 1993).
Biogeography
Cooper's hawks breed from British Columbia eastward to Nova Scotia and southward to northern Mexico and Florida (AOU 1998). Specifically, it nests from southern British Columbia, northwestern Montana, Wyoming, eastern North Dakota, southern Manitoba, western Ontario, northern Michigan, southern Ontario, Southern Quebec, Maine, and Nova Scotia, south to Baja California, south-central Texas, Louisiana, central Mississippi, central Alabama, and central Florida (Terres 1980; Reynolds 1975).
The species winters from British Columbia eastward to New England and southward primarily to Honduras (AOU 1998). The wintering range includes the area from Washington, Colorado, Nebraska, Iowa, southern Wisconsin, southern Minnesota, southern Michigan, southern Ontario, New York, southern Maine and Massachusetts south through the rest of the United States to Costa Rica (Terres 1980). The Cooper's hawk makes up a large part of the great fall flights of hawks that pass over the United States in September, they fly high and seem to prefer to fly when the wind is from the northwest (Bent 1937).
In California, the Cooper's hawk is a breeding resident throughout most of the wooded portion of the state. It breeds in the southern Sierra Nevada foothills, New York Mountains, Owens Valley, and other local areas in southern California. Its breeding range is from sea level to above 2,700 m (0-9000 ft). This species was once considered a common nester throughout California (Grinnell and Miller 1944). In southern California, the species is present year-round nearly throughout the state, except for the Colorado River and desert areas, where the species no longer breeds (Garrett and Dunn 1981). Although the Cooper's hawk breeds in southern California and has a year-round resident population, it also occurs in the region as a spring and fall migrant and as a winter resident (Garrett and Dunn 1981).
There is little available data on changes in the distribution of the Cooper's hawk. The species appears to be increasing in North Dakota and Minnesota (Rosenfield and Bielefeldt 1993).
Known Populations Within Western Riverside County
Cooper's hawks apparently may be found nearly throughout the Plan Area in appropriate woodland habitats (Patten, 1998, pers. comm.). Data records are located throughout much of the Plan Area except in the easternmost desert areas and some of the montane areas. The lack of data points within these areas may be due to low survey effort. Cooper's hawks have been documented that they may be found in all of the mountainous areas but they occur at low densities (Stephenson and Calcarone 1999). Many of these records may be for spring and fall migrating transients or a wintering population.
Locations of the Cooper's hawk appear to be concentrated along the Prado Basin/Santa Ana River, San Timoteo Canyon, Temescal Wash, Wasson Canyon, Slater Canyon, Santa Rosa Plateau West, Temecula Creek, Murrieta Creek, Tucalota Creek, Vail Lake, Wilson Valley, San Bernardino National Forest, and Cleveland National Forest. Important breeding populations include a large concentration in the Prado Basin and contiguous reaches of the Santa Ana River. Cooper's hawks also occur in woodland habitats (at least in winter) throughout the Plan Area. They have been recorded within shrubby habitats as well, probably as a foraging observation due to the lack of trees for nesting. Although surveys in the Prado Basin and contiguous reaches of the Santa Ana River have been adequate in recent years, surveys of similar intensity have not been conducted in other woodland areas throughout the large majority of the Plan Area.
Other geographic locations recorded within the U.C. Riverside database include: Box Springs Mountains, Mockingbird Canyon, El Cerrito, Lake Mathews-Estelle Mountain, Gavilan Hills, Motte-Rimrock Reserve, March ARB, Lake Perris, Mystic Lake/San Jacinto Wildlife Area, Quail Valley, Wildomar, Santa Rosa Plateau East, Sage, Lake Skinner, Badlands, Beaumont, Bautista Creek, Potrero Creek, and foothills of the Santa Ana Mountains.
Biology
Genetics: A presumed natural hybrid of the Cooper's hawk and northern goshawk was reported by Gray in 1958 (Terres 1980). A. cooperii, A. gundlachi, and A. bicolor comprise a super species apparently evolved from a common stock of tropical American accipiters (Brown and Amadon 1968).
Diet and Foraging: For the Cooper's hawk, avian prey items, especially passerines, comprise 70 percent of the number of food items and 58 percent of the dietary biomass delivered to Cooper's hawk broods at two nests surrounded by a mixed grass prairie with mammalian prey making up the remainder (Peterson and Murphy 1992). In general, during breeding and non-breeding, the Cooper's hawk uses avian prey predominantly, sometimes taking fish and mammals (Terres 1980). In comparison to the northern goshawk, the Cooper's hawk takes more avian prey (Bosakowski, et al. 1992b; Whaley and White, 1994). The Cooper's hawk catches small birds, especially young birds during the nesting season, and small mammals; it also takes reptiles and amphibians.
The Cooper's hawk hunts in broken woodland and habitat edges; it catches prey in the air, on the ground, and in vegetation. Sometimes it runs prey down in dense thickets. It uses cover to hide, attack, and approach prey; it also soars and makes low, gliding search flights (Zeiner, et al. 1990). It forages by dashing through the woods in a low, swift flight, around trees, through the brush and reaches out in the air or on the ground to catch avian prey with the talons (Terres 1980). After catching its prey, the Cooper's hawk may fly with the prey to a water source in order to drown it (Terres 1980).
Daily Activity: The Cooper's hawk is a year-long, diurnally active bird (Zeiner, et al. 1990).
Reproduction: The Cooper's hawk breeds primarily in riparian areas and oak woodlands and apparently is most common in montane canyons (Garrett and Dunn 1981; Hamilton and Willick 1996). It usually nests in second-growth conifer stands, or in deciduous riparian areas, usually near streams or open water (Zeiner, et al. 1990). Throughout much of the west, the Cooper's hawk nests in stands of cottonwoods along stream courses especially where the tree stands are fairly large (Call 1978). Denser stands of trees with moderate crown-depth are used for nesting. It appears that the vertical structure of the nest site tree is more important to the nest-site selection than the horizontal structure (Wiggers and Kritz 1991).
A study comparing nesting habits of Cooper's hawk and sharp-shinned hawk, found that Cooper's hawks tend to nest in stands with lower densities of taller and larger trees with a greater proportion of hardwood cover (Trexel, et al. 1999). It apparently does not tolerate nesting sharp-shinned hawks in the vicinity of its nest (Terres 1980).
In urban settings in Tucson, Arizona, Cooper's hawks have been found nesting mainly in eucalyptus (70.8 percent), aleppo pine (25.0 percent) and cottonwood trees (4.2 percent) (Boal, et al. 1998). Nest trees were found to be taller and of greater diameter than randomly sampled trees and thus had more canopy cover and the nest trees were often the largest tree in the nest site. Although nest sites were always in heavily forested areas, they were significantly closer to forest openings and wetland, were usually on level ground and were never located on a ridgeline or steep upper slope (Bosakowski, et al. 1992a).
The Cooper's hawk locates its nest on a horizontal limb of a pine or hardwood, near the trunk or in the crotch of a hardwood tree species, usually 10 to 60 feet above the ground and sometimes uses an old nest of a crow (Harrison 1978). It also often nests just below the lowest live limbs (Zeiner, et al. 1990). The nest is typically a platform of sticks and twigs lined with bark (Call 1978).
Cooper's hawk eggs are laid in February through June and the clutch size is 3 to 6 eggs; usually 4 to 5 eggs (Brown and Amadon 1968). Eggs are incubated mostly by the female for approximately 24 days (Terres 1980). Incubation is usually started after laying the third egg, thus hatching is asynchronous for the fourth and later eggs. The young birds usually depart the nest at 30 to 34 days but continue to be brought food for up to 7 weeks after leaving the nest.. The young may remain together near the nest for another 5 to 6 weeks (Rosenfield and Bielefeldt 1993). In rural Wisconsin, Rosenfield, et al. (1995) found a minimum intergeneration turnover time of six years for breeding Cooper's hawks.
Survival: One banded individual of the Cooper's hawk was recorded as being shot at 7 years 5 months old (Terres 1980). The maximum reported age is 12 years (Rosenfield and Bielefeldt 1993). The yearly fledging success is about 2 young/ pair with nesting success of 57 percent to 93 percent (Craighead and Craighead 1956; Rosenfield and Bielefeldt 1993). Mortality rates have been estimated as 72 percent to 78 percent in the first year, 34 percent to 37 percent thereafter (Rosenfield and Bielefeldt 1993).
Dispersal: Although it is mostly a year-long resident, some Cooper's hawks from more northern areas, migrate into California. The Cooper's hawk may also move downslope and south from areas of heavy snow and return to the general nesting area in the spring (Zeiner, et al. 1990). The mean distance from the natal site to the breeding site is 12 kilometers for males and 14.4 kilometers for females. Adult birds frequently reoccupy nesting areas and breeding site fidelity is assumed (Rosenfield and Bielefeldt 1993). The Cooper's hawk may reuse the same nest site for multiple years (Call 1978).
Socio-Spatial Behavior: Nest sites of the Cooper's hawk within stands of oaks are located approximately 2.7 kilometers (1.6 miles) apart and thus are distributed widely but sparsely within woodland habitat (Zeiner, et al. 1990). The seasonal home range size has been estimated at 784 hectares with the daily home range averaging 231 hectares (Murphy, et al. 1988). Cooper's hawks may require a minimum of 6 hectares (15 acres) of suitable, undisturbed timber for nesting (Call 1978). Rosenfield, et al. (1995) found a nesting density of 331 hectares/pair in a long-term study in rural Wisconsin. Studies of urban areas have reported a maximum density of 272 hectares/pair, according to this same study.
In Michigan, Craighead and Craighead (1956) measured four home ranges of Cooper's hawks that averaged 311 hectares (768 acres) and varied from 96-401 hectares (237-992 acres); they estimated that 17 other home ranges averaged 207 hectares (512 acres), and varied from 18-531 hectares (45-1312 acres). They reported one home range in Wyoming of 205 hectares (506 acres). Males defend an area about 100 meters (330 feet) around potential nest sites prior to pair formation (Brown and Amadon 1968). Nests in Oregon were 3.2 to 4.2 kilometers (2 to 2.6 miiles) apart (Jackman and Scott 1975). Elsewhere, nests have been reported 1.6 to 2.4 kilometers (1 to 1.5 miles) apart (Meng 1951, Brown and Amadon 1968). Of 77 territories in California, in oak stands, mean distance between nests was 2.6 kilometers (1.6 miles) (Zeiner, et al. 1990).
Community Relationships: The Cooper's hawk is an important predator of small birds. Nestlings and immatures not yet skilled at catching prey may be killed by ravens, northern goshawks, and great horned owls (Beebe 1974). The species may compete, to a limited extent, with sharp-shinned hawks and northern goshawks (Beebe 1974).
Although the northern goshawk is a potential competitor, niche overlap is reduced by using different habitats and by using different species of prey, different sizes of prey and by foraging in different zones (Bosakowski, et al. 1992b). The Cooper's hawk is determined to be more of a generalist from this study by having the greatest niche width. The study suggests that past and current competition may have been responsible for segregating the niches of the Cooper's hawk and northern goshawk. When compared to the sharp-shinned hawk, another potential competitor, the Cooper's hawk used mostly deformed nest trees and tended to place nests below the tree canopy (Wiggers and Kritz 1991).
Threats to Species
Recently there have been declines in the population of the Cooper's hawk in California (Remsen 1978). Previously judged to be relatively common to even abundant, for a raptor, in autumn in suitable habitat, southern California's breeding population of the Cooper's hawk reportedly has been reduced in recent decades, especially in lowland areas where much riparian woodland has been destroyed (Grinnell and Miller 1994; Garrett and Dunn 1981). Only approximately 40 pairs were detected in nearby Orange County during recent breeding bird atlas survey efforts there (Gallagher 1996). Habitat destruction, mainly in lowland riparian areas, due to urbanization and development is probably the main threat, although direct or indirect human disturbance at nest sites can be equally detrimental (Remsen 1978; Boal and Mannan, 1998).
Timber harvests may alter the suitability of nesting or foraging habitats as well as the prey populations on a local or regional scale but the magnitude and seasonality of such impacts are uncertain. Breeding and nest site habitats are diverse and apparently not limiting in some areas (Rosenfield and Bielefeldt 1993).
Other threats to the species include illegal Take of nestlings and to a less extent, the effects of pesticides (U.S.F.S. pers. comm. 1999). A serious decline occurred in the 1970s during the nesting season probably due to eggshell thinning resulting from pesticides (Terres 1980; Henny and Wight 1972).
Special Biological Considerations
Cooper's hawks occur in landscapes where wooded areas occur in patches and in groves, often using patchy woodlands and edges with snags (Beebe 1974). Many of the commonly used forest stand structural measurements, such as basal area and tree density, may not be adequate for predicting suitable accipiter nesting habitat (Siders and Kennedy 1996). Nesting and foraging usually occur near open water or within or near riparian vegetation (Zeiner, et al. 1990). It has been hypothesized that four factors affect the use of a stand of trees by nesting Cooper's hawks: stand type, stand density, stand age, and degree of fragmentation (Ehrlich and Drickamer 1993).
The Cooper's hawk population within the Prado Basin and surrounding Santa Ana River drainage apparently has increased within the Prado Basin during the course of 14 years of habitat and species conservation efforts and monitoring at that locale (L. R. Hays, USFWS, pers. obs.). Although fairly large when monitoring began in 1983, the Prado Basin/Santa Ana River Cooper's hawk population is even larger today.
Boal, et al. (1999) compared breeding ecology in urban and "exurban (i.e., undeveloped, natural)" areas in southeastern Arizona. His group found urban pairs to nest earlier, have a much higher nestling mortality (50.3 percent in urban settings compared with 4.9 percent in exurban areas), and a higher overall nest failure rate. The studied found urban nestlings to primarily die from trichomoniasis and that free-ranging Cooper's hawks in urban areas primarily die from collisions, most often with windows. In a separate study, Boal's team (1998) found urban nest trees in Tucson, Arizona to be in high-density residential area (65.9 percent) and high-use recreational areas (22.7 percent).
The type of response and intensity of the Cooper's hawk aggressive response to human intrusion near a nest site varies among individuals and probably also varies with the stage of nesting. Many breeding birds respond by remaining inconspicuous, neither vocalizing nor behaving aggressively in the presence of humans. Some individuals may leave the immediate vicinity of the nest, however, the human distance at which this behavior occurs has not been reported (Rosenfield et al. 1985). The implication of human intrusion into the nesting area of the Cooper's hawk is that the nesting attempt may fail, however these implications have not been reported to seriously impact the nesting success of the Cooper's hawk (Rosenfield et al. 1985).
In northern New Jersey, where, in 1993, only 18 nesting Cooper's hawks were known in the area, researchers recommended that any nest site occurring in a wilderness area be protected from habitat alterations within a 0.6 kilometer radius around the nest site (Bosakowski, et al. 1993).
Livestock exclosures, reforestation, and other measures have been suggested for riparian nesting habitat in some regions however there is no documentation of the relative effect of such measures. Timing timber harvests for the nonbreeding season or for stands that are unused by the Cooper's hawk may avoid impacts to known nests. Stands that have been thinned but not clear cut, if done during the nonbreeding season are then reoccupied the next season for breeding (Rosenfield and Bielefeldt 1993).
LITERATURE CITED
AOU (American Ornithologists' Union). 1998. Check-List of North American Birds. Seventh Edition. American Ornithologists' Union, Washington, D.C. 829 pp.
Beebe, F.L. 1974. Field studies of the Falconiformes of British Columbia. Brit. Col. Prov. Mus. Occas. Paper No. 17. 163 pp.
Bent, A. C. 1937. Life histories of North American birds of prey. Part 1, U. S. National Museum Bulletin. 170. 482pp.
Boal, C. W. and R. W. Mannan. 1998. Nest-site selection by Cooper's hawks in an urban environment. J. Wildl. Management 62: 864-871.
Boal, C. W. and R. W. Mannan. 1999. Comparative breeding ecology of Cooper's hawks in urban and exurban areas of southeastern Arizona. Journal of Wildlife Management : 63:77-84.
Bosakowski, T., R. Seiser, D. G. Smith and L.J. Niles. 1993. Loss of Cooper's Hawk nesting habitat to suburban development: Inadequate protection for a state-endangered species. Journal of Raptor Research.27: 26-30.
Bosakowski, T., D. G. Smith, and R. Speiser. 1992a. Nest sites and habitat selected by Cooper's hawks, Accipiter cooperii,à`Eánorthern New Jersey and southeastern New York. Canadian Field-Naturalist 106: 474-479.
Bosakowski, T., D. G. Smith, and R. Speiser. 1992b. Niche overlap of two sympatric-nesting hawks, Accipiter spp., in the New Jersey-New York highlands. Ecography 15: 358-372.
Brown, L., and D. Amadon. 1968. Eagles, hawks and falcons of the world. 2 Vols. Country Life Books, London. 945pp.
Call, M. W. 1978. Nesting Habitats and surveying techniques for common western raptors. Technical Note TN-316. U.S. Department of the Interior - Bureau of Land Management, Denver Service Center.
Craighead, J. J., and F. C. Craighead, Jr. 1956. Hawks, owls and wildlife. Stackpole Books, Harrisburg, PA. 443pp.
Ehrlich, R. M., and L. C. Drickamer. 1993. Habitats used for nesting by Cooper's hawks Accipiter cooperii in Southern Illinois. Transactions of the Illinois State Academy of Science 86: 51-62.
Gallagher, S. 1996. Orange County Breeding Bird Atlas. Sea and Sage Audubon Press, Santa Ana, California.
Garrett, K. and J. Dunn. 1981. Birds of Southern California: Status and Distribution. Los Angeles Audubon Society. 407 pp.
Grinnell, J. and A.H. Miller. 1944. The Distribution of the Birds of California. Pacific Coast Avifauna Number 27. Cooper Ornithological Club, Berkeley, California. Reprinted by Artemisia Press, Lee Vining, California; April, 1986. 617 pp.
Hamilton, R. and D.R. Willick. 1996. The Birds of Orange County, California: Status and Distribution. Sea and Sage Press, Irvine, California. 150 pp. with appendices.
Harrison, C. 1978. A field guide to the nests, eggs and nestlings of North American birds. W. Collins Sons and Co., Cleveland, OH. 416pp.
Hays, L. R. 1999. USFWS, pers. obs.
Henny, C. J., and H.M. Wight. 1972. Population ecology and environmental pollution; red-tailed and Cooper's hawks. Pages 229-249 in U.S. Fish and Wildlife Service. Population ecology in migrating birds. U.S. Dep. Inter., Fish and Wildl. Serv. Res. Rep. No. 2. Tech. Paper No. 2831.
Jackman, S. M., and J. M. Scott. 1975. Literature review of twenty-three selected forest birds of the Pacific Northwest. U.S. Dep. Agric., For. Serv., Reg. 6, Portland OR. 382pp.
Meng, H. K. 1951. The Cooper's hawk, Accipiter cooperii (Bonaparte). Ph.D. Thesis, Cornell Univ., Ithaca, NY. 202pp.
Murphy, R. K., M. W. Gratson, and R. N. Rosenfield. 1988. Activity and habitat use by a breeding male Cooper's hawk in a suburban area. J. Raptor Research 22: 97-100.
Patten, Michael. 1998. Riverside County Editor for American Field Notes and Past Secretary, California Birds Records Committee, pers. comm.
Peterson, D. J., and R. K. Murphy. 1992. Prey delivered to two Cooper's hawk Accipiter cooperii nests in northern mixed grass prairie. Canadian Field-Naturalist 106: 385-386.
Remsen, J. V. Jr. 1978. Bird Species of Special Concern in California. State of California. Department of Fish and Game. Supported by Federal Aid in Wildlife Restoration, Project Pr W-54-R-9, Nongame Wildlife Investigation, Wildlife Management Branch Administrative Report No. 78-1. 54 pp.
Reynolds, R. T. 1975. Distribution, density, and productivity of three species of Accipiter hawks in Oregon. M.S. Thesis, Oregon State Univ., Corvallis. 39pp.
Rosenfield, R. N., and J. Bielefeldt. 1993. Cooper's hawk (Accipiter cooperii). In The Birds of North America, No. 75 (A. Poole and F. Gill, eds.) The Academy of Natural Sciences, Philadelphia, PA and The American Ornithologists' Union, Washington D.C.
Rosenfield, R. N., J. Bielefeldt, J. L. Affeldt and D. J. Beckman. 1995. Nesting density, nest area reoccupancy and monitoring implications for Cooper's Hawks in Wisconsin. Journal of Raptor Research, v.9. n.1, 1995:1-4.
Rosenfield, R. N., J. Bielefeldt, R. K. Anderson, and W. A. Smith. 1985. Taped calls as an aid in locating Cooper's Hawk nests. Wildl. Soc. Bull. 13: 62-63.
Siders, M. S., and P. L. Kennedy. 1996. Forest structural characteristics of accipiter nesting habitat: Is there an allometric relationship? Condor 98: 123-132.
Stephenson, John r., and Gena M. Calcarone. 1999. Southern California mountains and foothills assessment: habitat and species conservation issues. General Technical Report GTR-PSW-172. Albany, CA: Pacific Southwest Research Station, Forest Service, U.S. Department of Agriculture. 402 pp.
Terres, J. K. 1980. The Audubon Society Encyclopedia of North American Birds. Alfred A. Knopf, New York, New York. 1109pp.
Trexel, D. R., R. N. Rosenfield, J. Bielefeldt, and E. A. Jacobs. 1999. Comparative nest site habitats in sharp-shinned and Cooper's hawks in Wisconsin. Wilson Bulletin 111: 7-14.
Whaley, W.H., and C.M. White. 1994. Trends in geographic variation of Cooper's hawk and northern goshawk in North America: A multi variate analysis. Proc. West. Found. Vert. Zool. 5:161-209.
Wiggers, E. P., and K. J. Kritz. 1991. Comparison of nesting habitat of coexisting sharp-shinned and Cooper's hawks in Missouri. Wilson Bulletin. 103: 568-577.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
double-crested cormorant (Phalacrocorax auritus)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
double-crested cormorant (Phalacrocorax auritus)
Status:
State: Species of Special Concern
Federal: None
GROUP DESIGNATION AND RATIONALE
Group 2
The double-crested cormorant has a wide distribution throughout the MSHCP Plan Area within suitable habitat. It occurs at every open water body within the Plan Area and thus uses habitat predictably and responds well to available suitable habitat. It will use habitat near open water bodies containing trees for creating rookeries. The only known nesting location in the Plan Area and any nesting locations found in the future will require site specific management.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area 16,100 acres of open water habitat within seven open water bodies and one drainage including Lake Mathews, Diamond Valley Lake, Lake Skinner, Lake Elsinore, Vail Lake, Lake Perris, Mystic Lake and Prado Basin/Santa Ana River and the wetland habitats within Prado Basin/Santa Ana River.
Objective 2
Include within the MSHCP Conservation Area the known double-crested cormorant rookery in the Prado Basin/Santa Ana River.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
For the purpose of the conservation analysis, potential habitat for the double-crested cormorant includes open water lakes and reservoirs, drainages supporting open water, and the wetland vegetation communities within the Prado Basin and Santa Ana River where nesting occurs. The double-crested cormorant has been documented to nest within the MSHCP Plan Area at the Prado Basin, and known foraging habitat and potential nesting habitat occur at the large lakes, reservoirs, and drainages supporting open water habitat within the Plan Area. Based on these habitats, the Plan Area supports approximately 18,280 acres of potential habitat for the double-crested cormorant. Table 1 shows the conservation and loss of potential habitat for the double-crested cormorant. Overall, approximately 16,100 acres (88 percent) of potential habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public Lands.
As described below under Data Characterization, 22 of the 56 recent point localities have a high location precision. These 22 point locations are distributed throughout the Plan Area within every open water body or drainage containing open water. Of these 22 point localities, 12 will be inside the Criteria Area or Public/Quasi-Public Lands. However, of the ten points located outside these preserved areas, the habitats for which they are mapped include existing residential/ urban/exotic areas, existing agriculture, or other upland habitats. These habitats do not constitute suitable habitat but these locations may have been of a bird flying overhead or within habitat adjacent to one of the reservoirs where they might hunt. Conservation of this species will generally be considered from a landscape perspective because the species is found throughout the Plan Area and is well documented for the type of habitat within which they forage.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
DOUBLE-CRESTED CORMORANT
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| All Bioregions | |||||||
| Open Water | 12,210 | 1,190 | 9,150 | 10,340 | 40 | 1,830 | 1,870 |
| Prado Basin/Santa Ana River | 6,070 | 550 | 5,210 | 5,760 | 0 | 310 | 310 |
| TOTAL | 18,280 | 1,740 (9%) |
14,360 (79%) |
16,100 (88%) |
40 (<1%) |
2,140 (12%) |
2,180 (12%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
In addition to the landscape focus on open water for foraging and nesting there are definable locations for focusing conservation efforts including the Prado Basin and Santa Ana River where nesting is documented to occur. These areas will be essential for conservation of the species and a total of 5,760 acres of wetland habitats located within the Prado Basin/Santa Ana River will be conserved as Criteria Area and Public/Quasi-Public Lands. Any nesting locations, if they were to be identified in the future, will be important to consider for conservation.
In addition, the Riparian/Riverine Areas and Vernal Pools policy described in Section 6.1.2 provides for conservation of wetlands which provide habitat for this species through avoidance and minimization. Mitigation for impacts to wetlands shall be incorporated in accordance with the "No Net Loss" policy of federal and state wetland regulations. The proposed mitigation shall be directly related to the functions and values of the wetland as related to this species and result in equivalent replacement.
MSHCP Conservation Area Configuration Issues
Several large blocks of habitat supporting the current known nesting and foraging locations and potential foraging and nesting locations of the double-crested cormorant will be conserved as Criteria Area and Public/Quasi-Public Lands, including the Prado Basin/Santa Ana River, Lake Skinner, Diamond Valley Lake, Lake Mathews, Mystic Lake/San Jacinto Wildlife Area, Lake Perris, Lake Elsinore, Vail Lake, Bautista Creek, San Timoteo Creek, Temecula Creek, Murrieta Creek, and San Jacinto River. As identified below, the dispersal distance for the species, 5 to 10 miles, will allow them to cover the MSHCP Plan Area and they will be capable of dispersing from a nest site to forage in any part of the Plan Area. As such, the MSHCP Conservation Area will provide adequate habitat for foraging during nomadic visits to the area and migratory stopovers as well as habitat containing known and potential nest sites with adequate protection around each nest site and foraging areas during the breeding season. Foraging areas are provided at the open water bodies including Vail Lake, Lake Skinner, Diamond Valley Lake, Mystic Lake, Lake Perris, Lake Elsinore, Lake Mathews, Prado Basin/Santa Ana River. Foraging habitat is also provided in drainages containing open water including Bautista Creek, San Timoteo Creek, Temecula Creek, Murrieta Creek, and San Jacinto River. Potential and known nest sites are provided at these open water/reservoirs and within the MSHCP Conservation Area, especially in the Prado Basin area, in the form of large trees or snags. These MSHCP Conservation Area areas are linked as well, however the double-crested cormorant, due to its ability to move long distances, may rely less on the linkage than other species.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 16,100 acres of suitable Conserved Habitat (open water and wetland habitat within the Prado Basin/Santa Ana River) and the known rookery location in the Prado Basin/Santa Ana River. The current population size of the double-crested cormorant is unknown, however it appears to have regular use of specified areas and a known breeding location that has been regularly monitored in the past.
INCIDENTAL TAKE
The estimated Take of the double-crested cormorant is based on the acreage of potentially suitable and/or occupied habitat. About 2,180 acres of potential habitat for the double-crested cormorant will be outside the Criteria Area and Public/Quasi-Public Lands and individuals located within these areas will be subject to Incidental Take consistent with the Plan. This comprises approximately 12 percent of the total potential habitat. This includes the open water bodies composed of Hemet Lake, and Lake Riverside.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The UCR location database includes approximately 67 records for the double-crested cormorant within the Plan Area dated from 1900 to 1999. Approximately 56 records are relatively recent (dated from 1990) and of these recent records, 22 are high precision records that can be accurately placed within the area. The habitat types associated with these recent and high precision data records include alluvial, agriculture, riparian, sage scrub, open water, and residential. The residential habitat records may reflect records that are either no longer extant or where the location is a small pocket of suitable habitat within or adjacent to a developed area or a residential area adjacent to an open water body.
The literature available on the double-crested cormorant is relatively low. It is focused on the natural history of the species, however, some of the details of its natural history have not been determined. A few general ornithological reference treatments have been prepared for the species. Little information is available with respect to the Plan Area other than general distribution and occurrence information.
Habitat and Habitat Associations
The double-crested cormorant is a common inhabitat of seacoasts and inland waters, rarely observed out of sight of land. They may be seen swimming low in the water, often with little more than their heads and necks showing (Hatch and Weseloh 1999). As summarized by Zeiner et al. (1990), double-crested cormorants require lakes, rivers, reservoirs, estuaries, or use the ocean for foraging. It occupies diverse aquatic habitats in all seasons and requires, in addition to feeding habitats, suitable places for daytime resting or loafing and nighttime roosts (Hatch and Weseloh 1999). Double-crested cormorants nest on the mainland in tall trees, wide rock ledges on cliffs, or rugged slopes near (or in) the aquatic environments. The species rests in the daytime and roosts overnight beside the water on offshore rocks, islands, steep cliffs, dead branches of trees, wharfs, jetties, or even transmission lines. Its perching sites must be barren of vegetation (Bartholomew 1943). It must have nearby access to perches which it visits periodically in the day to dry its plumage. Sometimes it rests, or even sleeps, on the water in the daytime (Palmer 1962). It requires a considerable length of water, or an elevated perch, for a labored and lengthy take-off. For its habitat, the species also requires undisturbed nest-sites beside the water, on islands or the mainland. The suitable nest-site must be within 8-16 kilometers (5-10 miles) of a dependable food supply (Palmer 1962).
Biogeography
Double-crested cormorants breed from Alaska eastward to Newfoundland southward, in isolated colonies, to California, Florida, Mexico and Belize. It is located along the entire Pacific coast from the Aleutians to southern Baja and along the Atlantic coast from Newfoundland south to Florida (Terres 1980). The species winters from Alaska eastward to New England southward to California, Florida, Mexico, and Belize but is absent from the northernmost portion of the breeding range (AOU 1998).
Zeiner, et al. (1990) summarize the distribution, abundance, and seasonality of the double-crested cormorant within California as follows. It is a year-long resident along the entire coast of California and on inland lakes, and seasonally increases in population size as migrant populations winter in the area. During August to May, it is fairly common to locally very common along the coast and in estuaries and salt ponds; it is uncommon in marine subtidal habitats from San Luis Obispo County south, and very rare to the north. In the same season, it is fairly common at the Salton Sea and Colorado River reservoirs, and rare to fairly common in lacustrine and riverine habitats of the Central Valley and coastal slope lowlands. It is less common in the summer, except it is locally common near nesting colonies. In southern California, the species is considered a year-round resident (Garrett and Dunn 1981). Although double-crested cormorants are present in suitable habitats throughout southern California, rookeries are extremely scarce away from the Salton Sea, the Colorado River, and the Channel Islands (Garrett and Dunn 1981).
Known Populations Within Western Riverside County
Although double-crested cormorants may be found year-round nearly throughout the Plan Area in appropriate habitats, there is only one known rookery located in the Prado Basin (L.R. Hays, USFWS, pers. obs.; Michael Patten, Riverside County Editor for American Field Notes and Past Secretary, California Bird Records Committee, pers. comm., 1998). Approximately 40 pairs bred in the Prado Basin during the 1998 breeding season (James Pike, USFWS, pers. comm., 1998). Other localities where the species is regularly observed include Lake Mathews, Lake Perris, Lake Skinner, and Lake Elsinore. These occurrences are likely to be foraging or wintering individuals and they probably use these locations, as well as other lakes/reservoirs, on a regular basis.
Geographic locations recorded within the U.C. Riverside database include: Prado Basin, Santa Ana River, Lake Mathews, Lake Elsinore, Santa Rosa Plateau, Temecula Creek, Lake Skinner, Wilson Valley, Lake Hemet, Lake Perris, San Jacinto Wildlife Area, and San Timoteo Creek.
Biology
Genetics: The double-crested cormorant is thought to be closely related to the neotropic cormorant (Hatch and Weseloh 1999). A phylogenetic analysis of osteological characters by Siegel-Causey (1988) placed the double-crested cormorant with the neotropic cormorant and three species from Australia and India in the genus Hypoleucos.
Diet and Foraging: Double-crested cormorants are strictly piscivorous (Robertson 1974, Cogswell 1977, Neuman et al. 1997) and thus require lakes, rivers, reservoirs, estuaries, or the ocean for foraging. Foraging occurs mainly in daylight hours (Blackwell and Krohn 1997). In areas where fish populations are augmented (e.g., trout stocking) feeding is affected. For example, cormorants were found eating mainly suckers (Catastomus spp.) before trout stocking, but trout-consumption increased from 17 percent to 60 percent after stocking (Derby and Lovvorn 1997). Foraging in this species is opportunistic and flexible: more than 250 species of fish from over 60 families have been reported as prey (Hatch and Weseloh 1999). Supply of prey can dictate habitat selection and occurrence of cormorants (Blackwell and Krohn 1997).
While foraging, the double-crested cormorant dives from the water surface and pursues prey underwater, usually remaining submerged for about 30 seconds. It prefers water less than 9 meters (30 feet) deep with a rocky or gravel bottom, but may catch fish as deep as 22 meters (72 feet). Sometimes the species feeds cooperatively in flocks of up to 600 individuals, often with pelicans (Zeiner et al. 1990). It generally feeds in shallow, open water and close to shore. It may feed over sandy bottoms or among rocks and in beds of sea grass or kelp (Hatch and Weseloh 1999).
Daily Activity: Foraging activity of the double-crested cormorant during the winter can occupy, on average, 17.7 percent of a cormorant's daily activity (King, et al. 1995). It frequently rests in the daytime and migrates both day and night (Zeiner, et al. 1990).
Reproduction: Double-crested cormorants nest on the mainland in tall trees near (or in) aquatic environments. Males typically arrive at the nesting area first unpaired. Advertising displays by the males and courtship are evident at the nest site shortly after arrival. Both members of the pair build a new nest, or repair an old one. The nest is often sufficiently complete within two to four days for egg-laying (Hatch and Weseloh 1999). The double-crested cormorant may nest on the ground or cliffs, in trees or shrubs, or on artificial nest structures and transmission line towers, and also on abandoned wharves or on bridges (Hatch and Weseloh 1999). Arboreal nests are placed 0.5 to 30 meters above ground in forks of branches or adjacent to the trunks. Zeiner et al. (1990) summarize breeding information as follows. It breeds mostly from April to July or August, but begins in January at the Salton Sea and Colorado River. Most of the egg-laying is from April to June. The species is monogamous; it nests in colonies of a few to hundreds of pairs, or even thousands; there is little current information on the sizes of California colonies. The clutch size is usually 3-4 eggs, the range is 2-7 eggs, possibly as high as 9 eggs. They are single-brooded. Incubation is 24.5-29 days. The altricial young are tended by both parents, and first fly at 5-6 weeks, and are fully independent at 10 weeks. The number of chicks fledged per nest in several San Francisco populations varied from 0.61 to 1.70 (Stenzel, et al. 1995). The cormorant usually breeds first at 3 years, sometimes at 2 years. About 25 percent of adults at breeding colonies are prebreeders (Lewis 1929, Mendall 1936).
Survival: The oldest banded double-crested cormorant has been recorded as 17 years and nine months (Klimkiewicz and Futcher 1989). Van der Veen (1973) estimated first-year survival of 0.48, second year of 0.74, and subsequent annual suvival of 0.85 with a mean adult life expectancy of 6.1 years. For studies on annual reproductive success, the hatching success is typically 50 to 75 percent; fledging success is 1.2 to 2.4 young per nest or 74 to 95 percent. Chick loss from the hatching to fledging periods is often low, measured at 5 percent in coastal British Columbia (Drent et al. 1964).
Dispersal: During the winter, cormorants move, on average, 15.7 kilometers from their night roost to a foraging location (King, et al. 1995). Individuals do not show fidelity to a roost site however, in stable populations, natal philopatry is probably high (King 1996). New colonies are thought to be formed by young birds, often at sites they have used as roosts or loafing areas, which may be the closest suitable habitat to the natal colony (Hatch and Weseloh 1999). Individuals forage far from the colony or roosts. Birds followed by airplane in Wisconsin flew an average of less than 3 kilometers from the breeding colony to the first foraging site and some individuals flew as far as 30 kilometers (Hatch and Weseloh 1999).
Socio-Spatial Behavior: The double-crested cormorant usually forages within 8-16 kilometers (5-10 miles) of the roost or nest colony (Palmer 1962). In Manitoba, the spacing of ground nests on islands averaged 1 per 0.8 square meters (9 feet) (McLeod and Bondar 1953). The defended territory is reported only at the nest, where a small area is actively defended within beak range (Siegel-Causey and Hunt 1986). The territory is used for some courtship displays, copulation, and nesting; it consists of the nest, and a perch for the non-incubating parent (Palmer 1962). In Saskatchewan, ground nests on islands were 22-38 centimeters (8.5-15 inches) in diameter, and ranged from 0-91 centimeters (0-36 inches) apart, measured from rim to rim (Vermeer 1970).
Community Relationships: The double-crested cormorant may hunt cooperatively with pelicans (Zeiner et al. 1990). The species is generally very gregarious throughout the year. They typically form dense nocturnal roosts, diurnal loafing areas, and breeding colonies (Hatch and Weseloh 1999).
Threats to Species
Judging from historical reports of huge migratory flocks blocking out the sun in the Mississippi River Valley (Robbins 1991), the double-crested cormorant has undoubtedly undergone a spectacular population decline in this century. One flight in La Crosse, Wisconsin on 24 April 1926 "continued for two and one-half hours, more or less intermittently, although there were always from a dozen to hundreds of large flocks in the air. The number of birds is variously estimated at from 100,000 to 1,000,000 birds"(Mark Byers, La Crosse Tribune, as quoted in Robbins 1991). By the 1960s, breeding colonies were limited to two counties in Wisconsin and only three to five birds were seen outside the few breeding colonies. By 1973, the species became a candidate for the [Wisconsin] endangered species list. Marked reductions in species numbers and inland breeding colonies in California also were noted as early as the early 1940's (Grinnell and Miller 1944). Although habitat destruction and persecution are implicated in the species' decline, environmental contaminants (such as persistent pesticides) and disease are also problematical, as is evidenced by a recent, massive die-off of the species at the Salton Sea (USFWS, unpublished data). Numbers of the double-crested cormorant have steadily been increasing since about 1975. Explanations arise from lowered mortality from pesticides and from the direct killing that was characteristic of earlier decades, increased food in the breeding season, and enhanced overwintering survival of adults and young (Hatch and Weseloh 1999).
Current declines in Washington, British Columbia and Baja California, may be explained by apparent movements of nesting birds during El Niño oceanographic conditions, habitat loss at interior colonies, and use of artificial nesting habitats (Carter, et al. 1995).
Many nesting colonies in California have been abandoned after human disturbance and habitat destruction (Remsen 1978). In Quebec, human disturbance of breeding colonies caused nest abandonment and increased predation by gulls on eggs and young (Ellison and Cleary 1978). Predation on eggs and young by gulls and crows may be an important factor reducing nesting success (Ellison and Cleary 1978, Siegel-Causey and Hunt 1981).
Special Biological Considerations
Currently, the double-crested cormorant may still be perceived as a pest of aquaculture in the southern United States and thus may receive some persecution. Management activities aimed at balancing cormorant and fish populations have been evaluated by researchers as poor and lacking scientific basis (Nisbet 1995). Future management responsibilities will be directed at balancing human interests and wildlife needs (Acord 1995). Owing to their economic impacts in some regions, further investigations are needed under controlled conditions to determine the effects of fish harvest rates by cormorants on overall production in ponds (Erwin 1995). The efficacy of providing alternative wetland feeding sites for cormorants is an area that requires more investigation. Birds may be lured away from catfish farms by nearby created wetlands (Erwin 1995).
The double-crested cormorant rookery in the Prado Basin is one of very few on the coastal slope of southern California away from the sea. The Prado Basin colony and a rookery consisting of approximately 40 pairs at Anaheim Lakes in Orange County apparently are the only breeding areas in or near the Los Angeles Basin (Gallagher 1997).
Increased populations sizes of the double-crested cormorant in the Great Lakes ecosystem have been attributed to a reduction in levels of organochlorine contaminants, reduction in human persecution and an increase in the availability of "forage-base fish" (Weseloh and Ewins 1994). Construction of irrigation reservoirs in Wyoming accounted for large, recent breeding population increases (Findholt 1988). However, these populations may not be sustainable if nest trees or nesting islands either decay or are eliminated by excessively high or low water levels (Findholt 1988).
LITERATURE CITED
Acord, B. R. 1995. Cormorant management and responsibilities: United States Department of Agriculture. Colonial Waterbirds 18 (Special Publication): 231-233.
AOU (American Ornithologists' Union). 1998. Check-List of North American Birds. Seventh Edition. American Ornithologists' Union, Washington, D.C. 829 pp.
Bartholomew, G. A., Jr. 1943. The daily movements of cormorants on San Francisco Bay. Condor 45:3-18.
Blackwell, B. F. and W. B. Krohn. 1997. Spring foraging distribution and habitat selection by double-crested cormorants on the Penobscot River, Maine, USA. Colonial Water birds 20:66-76.
Carter, H. R., A. L. Sowls, M. S. Rodway, U. W. Wilson, R. L. Lowe, G. J. McChesney, F. Gress, and D. W. Anderson. 1995. Population size, trends and conservation problems of the double-crested cormorant on the Pacific coast of North America. Colonial Waterbirds 18:189-215.
Cogswell, H. L. 1977. Water birds of California. Univ. California Press, Berkeley. 399pp.
Derby, C. E. and J. R. Lovvorn. 1994. Predation on fish by cormorants and pelicans in a cold-water river: A field and modeling study. Canadian Journal of Fisheries and Aquatic Sciences 54:1480-1493.
Drent, R., G. F. van Tets, F. Tompa, and K. Vermeer. 1964. The breeding birds of Mandarte Island, British Columbia. Can. Field-Nat. 78: 208-261.
Ellison, L. N., and L. Cleary. 1978. Effects of human disturbance on breeding of double-crested cormorants. Auk 95:510-517.
Erwin, R. M. 1995. The ecology of cormorants: some research needs and recommendations. Colonial Waterbirds 18 (Special Publication): 240-246.
Findholt, S. L. 1988. Status, distribution and habitat affinities of double-crested cormorant nesting colonies in Wyoming, USA. Colonial Waterbirds 11: 245-251.
Gallagher, S. 1997. Breeding Bird Atlas (Orange County). Sea and Sage Audubon Press, Santa Ana, California. 264 pp.
Garrett, K. and J. Dunn. 1981. Birds of Southern California: Status and Distribution. Los Angeles Audubon Society. 407 pp.
Grinnell, J. and A.H. Miller. 1944. The Distribution of the Birds of California. Pacific Coast Avifauna Number 27. Copper Ornithological Club, Berkeley, California. Reprinted by Artemisia Press, Lee Vining, California; April 1986. 617 pp.
Hatch, J. J. and D. V. Weseloh. 1999. Double-crested Cormorant. Birds of North America 441:1-36.
Hays, L. 1999. Pers. Comm. U.S. Fish and Wildlife Service.
King, D. T. 1996. Movements of double-crested cormorants among winter roosts in the Delta Region of Mississippi. Journal of Field Ornithology 67:205-211.
King, D. T., J. F. Glahn and K. J. Andrews. 1995. Daily activity budgets and movement of winter roosting double-crested cormorants determined by biotelemetry in the Delta region of Mississippi. Colonial Waterbirds 18:152-157.
Klimkiewicz, M. K., and A. G. Futcher. 1989. Longevity records of North American birds. Suppl. 1. J. Field Ornithol. 60: 469-494.
Lewis, H. F. 1929. The natural history of the double-crested cormorant (Phalacrocorax auritus auritus). Ru-Mi-Lou Books, Ottawa. 94pp.
McLeod, J. A., and G. F. Bondar. 1953. A brief study of the double-crested cormorant on Lake Winnipegosis. Can. Field-Nat. 67:1-11.
Mendall, H. L. 1936. Home life and economic status of the double-crested cormorant. Univ. Maine Studies, Second Ser., No. 38. 159pp.
Neuman, J., D. L. Pearl, P. J. Ewins, R. Black, D. V. Weseloh, M. Pike and K. Karwowski. 1997. Spatial and temporal variation in the diet of double-crested cormorants breeding on the lower Great Lakes in the early 1990s. Canadian Journal of Fisheries and Aquatic Sciences 54:1569-1584.
Nisbet, I C T. 1995. Biology, conservation and management of the double-crested cormorant: Symposium summary and overview (The double-crested cormorant: Biology, conservation and management, Colonial Waterbird Society Annual Meeting, University of Mississippi, Oxford, Mississippi, USA, October 14-18, 199). Colonial Waterbirds 18:247-252.
Palmer, R. S., ed. 1962. Handbook of North American birds. Vol. 1. Yale University Press, New Haven, CT. 567pp.
Patten, Michael. 1998. Pers. Comm. Riverside County Editor for American Field Notes and Past Secretary, California Bird Records Committee
Pike, J. 1998. Pers. Comm. USFWS.
Remsen, J. V., Jr. 1978. Bird species of special concern in California. Calif. Dept. of Fish and Game, Sacramento. Wildl. Manage. Admin. Rep. No. 78-1. 54pp.
Robbins, S. 1991. Wisconsin Bird life. The University of Wisconsin Press, Madison. 702 pp.
Robertson, I. 1974. The food of nesting double-crested and pelagic cormorants at Mandarte Island, British Colombia, with notes on feeding ecology. Condor 76:346-348.
Siegel-Causey, D. 1988. Phylogeny of the Phalacrocoracidae. Condor 90: 885-905.
Siegel-Causey, D., and G. L. Hunt. 1981. Colonial defense behavior in double-crested and pelagic cormorants. Auk 98:522-531.
Siegel-Causey, D., and G. L. Hunt. 1986. Breeding-site selection and colony formation in double-crested and pelagic cormorants. Auk 103: 230-234.
Stenzel, L. E., H. R. Carter, R. P. Henderson, S. D. Emslie, M. J. Rauzon, G. W. Page, and P. Y. O'Brien. 1995. Breeding success of double-crested cormorants in the San Francisco Bay area, California. Colonial Water birds 18:216-224.
Terres, J. K. 1980. The Audubon Society Encyclopedia of North American Birds. Alfred A. Knopf, New York, New York. 1109pp.
Van der Veen, H. E. 1973. Some aspects of the breeding biology and demography of the double-crested Cormorants (Phalacrocorax auritus) of Mandarte Island. Ph.D. thesis, Zoologisch Laboratorium der Rijksuniversiteit te Groningen, Groningen.
Vermeer, K. 1970. Some aspects of nesting of double-crested cormorants at Cypress Lake, Saskatchewan in 1969, a plea for protection. Blue Jay 28:11-13.
Wesloh, D. V. C. and P. J. Evans. 1994. Characteristics of a rapidly increasing colony of double-crested cormorants in Lake Ontario: Population size, reproductive parameters and band recoveries. Journal of Great Lakes Research 20:443-456.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
downy woodpecker (Picoides pubescens)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
downy woodpecker (Picoides pubescens)
Status:
State: None
Federal: None
GROUP DESIGNATION AND RATIONALE
Group 2
The downy woodpecker is sparsely distributed throughout the MSHCP Plan Area within suitable habitat. There are several areas that appear to be Core Areas including Prado Basin/Santa Ana River, Temescal Canyon, Alberhill Creek, Temecula Creek, and the Vail Lake area. It also occurs in other areas of the Plan Area including but not limited to San Timoteo Creek, the Badlands, Potrero, the mountain Bioregions, and Wilson Valley. Because it is well known for using riparian scrub, forest and woodland, and oak woodland and forest, occurs in all Bioregions of the Plan Area with known Core Areas, a landscape level of management with site specific requirements is proposed.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 34,080 acres of suitable nesting and foraging habitat for the downy woodpecker including riparian scrub, forest and woodland, and oak woodland and forest.
Objective 2
Include within the MSHCP Conservation Area the 5 Core Areas and linkages within the Prado Basin/Santa Ana River (9,670 acres), Vail Lake (Subunit 3 of the Southwest Area Plan; 12,320 acres), Temescal Wash (Subunit 3 of the Temescal Canyon Area Plan; 4,010 acres), Alberhill Creek (Subunit 2 of the Elsinore Area Plan; 3,460 acres), and Temecula Creek (Subunit 2 of the Southwest Area Plan; 850 acres).
Objective 3
Include within the MSHCP Conservation Area the micro-habitat (i.e., groups of large snags) in potential nesting habitat.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
For the purpose of the conservation analysis, potential habitat for the downy woodpecker includes riparian scrub, woodland, and forest, and oak woodland and forest habitat in all Bioregions within the Plan Area. The preferred habitat for the downy woodpecker, ecotones rather than forested areas and ecotones with a mixture of forest shrub and grasslands rather than either forest or forest/shrub ecotones (Brenner, et al. 1992) is embedded within the potential habitat analyzed for this species. The vegetation mapping for the Plan Area is not of a suitable fine scale to quantify the specific sub-habitat preferred by the downy woodpecker, however this sub-habitat of ecotones is included with the habitats analyzed for this species. Based on these habitats, the Plan Area supports approximately 46,790 acres of potential habitat for the downy woodpecker. Table 1 shows the conservation and loss of potential habitat for the downy woodpecker. Overall, approximately 34,080 acres (73 percent) of potential habitat in the Plan Area will be conserved in Criteria Area (6,310 acres or 13 percent) or existing Public/Quasi-Public Lands (27,770 acres or 59 percent). Within this potential habitat, areas containing groups of snags which provide the micro-habitat that is preferred by this species will be conserved.
This species occurs within the Forest Service lands as well as the lowland Bioregions as a breeding and wintering species. It occurs predominantly within riparian scrub, woodland and forest, and oak woodland and forest. Under the existing Forest Land allocation plan, these locations and habitats generally are located within the San Jacinto Wilderness area, the San Mateo Canyon Wilderness Area, and in most of the grazing allotments in both National Forests. Although it has been documented to occur in relatively low numbers at the higher elevations (below 2,000 meters) within the San Bernardino and Cleveland National Forest, the downy woodpecker is not documented to have Core Areas within these lands (Garrett and Dunn 1981). However, conservation of riparian and woodland habitats within the Cleveland National Forest and San Bernardino National Forest are important conservation areas for the downy because suitable habitat is present within these areas and it has been recorded within the mountain Bioregions up to 2,000 meters (Garrett and Dunn 1981).
TABLE 1
SUMMARY OF HABITAT CONSERVATION
DOWNY WOODPECKER
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| All Bioregions | |||||||
| Riparian Scrub, Woodland, Forest | 14,610 | 3,920 | 7,270 | 11,190 | 370 | 3,050 | 3,420 |
| Oak Woodlands and Forest | 32,180 | 2,390 | 20,500 | 22,890 | 5,020 | 4,270 | 9,290 |
| TOTAL | 46,790 | 6,310 (14%) |
27,770 (59%) |
34,080 (73%) |
5,390 (12%) |
7,320 (16%) |
12,710 (27%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
In addition, the Riparian/Riverine Areas and Vernal Pools policy described in Section 6.1.2, MSHCP Volume 1, provides for conservation of wetlands which provide habitat for this species through avoidance and minimization. Mitigation for impacts to wetlands shall be incorporated in accordance with the "No Net Loss' policy of federal and state wetland regulations. The proposed mitigation shall be directly related to the functions and values of the wetland as related to this species and result in equivalent replacement.
As described below under Data Characterization, 34 of the 65 relatively recent point localities have a high location precision. Of these 34 point localities, 10 (29 percent) will be inside the Criteria Area and 12 (35 percent) are located within Public/Quasi-Public Lands. One point location (3 percent) will be in the Rural/Mountainous zone. Of the 11 high precision recent points located outside the MSHCP Conservation Area, one point is located within suitable habitat composed of riparian habitat and the balance are located outside suitable habitat areas within existing residential/urban/exotic areas, non-native grassland, croplands, or Riversidean sage scrub. It is likely that many of the point locations are within riparian habitat and some of these may be inside the MSHCP Conservation Area but do not appear to be due to mapping scale. Conservation of this species will be considered from a landscape perspective, especially in the more western lowlands along the Interstate 15/215 corridor. This is largely due to the fact that the suitable habitat has been well defined and providing additional suitable habitat that is not currently occupied may assist with the recovery of the species.
In addition, there are definable locations for focusing conservation efforts that contain the downy woodpecker including Prado Basin/Santa Ana River (9,670 acres), Vail Lake (Subunit 3 of the Southwest Area Plan; 12,320 acres), Temescal Wash (Subunit 3 of the Temescal Canyon Area Plan; 4,010 acres), Alberhill Creek (Subunit 2 of the Elsinore Area Plan; 3,460 acres), and Temecula Creek (Subunit 2 of the Southwest Area Plan; 850 acres). A total of 30,310 acres of Core Areas will be included within the MSHCP Conservation Area. Conservation is also provided in areas that are occupied by the downy woodpecker but that are not Core Areas including San Timoteo Creek, the Badlands, Potrero, Wilson Valley, and drainages and woodland areas within the Cleveland National Forest and San Bernardino National Forest.
MSHCP Conservation Area Configuration Issues
Several large blocks of habitat supporting or potentially supporting the downy woodpecker will be conserved as Criteria Area or Public/Quasi-Public designations, including the Core Areas at Prado Basin/Santa Ana River, Temescal Wash, Alberhill Creek, Temecula Creek, and Vail Lake area. Other large blocks of habitat that support locations and/or contain potential habitat for this species will also be conserved including San Timoteo Creek, the Badlands, Potrero, Wilson Valley, and riparian habitat and drainages within the Cleveland National Forest and San Bernardino National Forest. Other areas containing few or old records for the downy woodpecker and contain potential habitat include Lake Mathews-Estelle Mountain, San Jacinto Wildlife Area/Lake Perris, Sycamore Canyon Regional Park, and Lake Skinner. The following large blocks of habitat have not been mapped as containing downy woodpeckers: Bautista Creek, Reche Canyon, Wasson Canyon, upper San Jacinto River, Murrieta Creek, and Santa Rosa Plateau Nature Preserve. However, these habitat blocks may have smaller riparian systems that contain potentially suitable habitat and could be occupied by downy woodpeckers currently or in the future.
As such, the MSHCP Conservation Area will provide adequate habitat linkages between core habitat areas for this species and will include smaller drainages that may support small numbers of the species. The Prado Basin Core Area is linked along the Santa Ana River to San Bernardino and Orange counties. This riparian area is linked to the south by the Temescal Wash to Lake Mathews and Lake Elsinore. Riparian habitat within the Vail Lake area is linked to the Lake Skinner-Diamond Valley Lake area via Tucalota Creek and to the San Bernardino National Forest. The Vail Lake area is also linked to the Santa Rosa Plateau and then to the Cleveland National Forest by the riparian habitat in Temecula Creek. The Badlands area provides a major habitat block that provides a linkage to Potrero Creek, Lake Perris, and the San Jacinto Wildlife Area.
Conservation Summary
In summary, conservation for this species will be achieved by the inclusion of at least 34,080 acres of suitable Conserved Habitat in the MSHCP Conservation Area. In addition, implementation of Objective 3 for this species will conserve the micro-habitat (i.e., groups of large snags) in potential nesting habitat. Five of the Core Areas of the downy woodpecker are conserved within large blocks of habitat in the MSHCP Conservation Area and additional areas with few or no recorded locations but that contain potential habitat are also conserved.
INCIDENTAL TAKE
About 12,710 acres (about 27 percent) of potential habitat for the downy woodpecker will be outside the Criteria Area or Public/Quasi-Public designations, and individuals within these areas will be subject to Incidental Take consistent with the Plan. None of the Core Areas will be outside the MSHCP Conservation Area. Of this, approximately 5,390 acres (12 percent) of potential habitat are located within Rural/Mountainous designation areas. While the Rural/Mountainous areas are not included within the MSHCP Conservation Area and will not be managed for the benefit of wildlife, the anticipated levels of development in these areas will likely be consistent with maintaining some habitat for the downy woodpecker.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The UCR location database includes approximately 84 records for the downy woodpecker within the Plan Area dated from 1888 to 2000. A total of approximately 65 records are relatively recent (within the past 10 years) and of these recent records, approximately 34 are high precision records that can be accurately placed within the area. The habitat types associated with these recent and high precision data records include riparian habitat, residential, cropland, grassland, sage scrub, and chaparral. The residential and more upland habitat records may reflect records that are either no longer extant or that are located in a small pocket of suitable habitat within or adjacent to a developed area or upland habitat.
The literature available on the downy woodpecker is relatively low. It is focused on the natural history of the species, however, due to its secretive nature, some of the details of its natural history have not been determined. A few general ornithological reference treatments have been prepared for the species. Little information is available with respect to the Plan Area other than general distribution and occurrence information.
Habitat and Habitat Associations
Downy woodpeckers as a whole may nest in deciduous and mixed deciduous coniferous woodland, riparian woodland, second growth, parks, and orchards (AOU 1998). Within southern California, the species generally nests in deciduous (often willow) woodlands, deciduous growth/oak woodlands, orchards, suburban plantings, and occasionally in conifers (Garrett and Dunn 1981). Grinnell and Miller (1944) previously reported that lowland stream-bottoms constitute the main theaters of activity for this woodpecker. Available water may be a factor for presence of the downy woodpecker (Zeiner et al. 1990). This species is a year-long resident of riparian deciduous and associated hardwood and conifer habitats and orchards. It requires abundant snags, and tree/shrub, tree/herbaceous, and shrub/herbaceous ecotones (Zeiner, et al. 1990). Abundance of downy woodpeckers has been correlated with occurrence of large snags and logs (Stark, et al. 1998). This study showed the species to prefer bottomland hardwood forests during both summer and winter seasons. Another study showed that the species prefers ecotones over forested areas and ecotones with a mixture of forest shrub and grasslands more than either forest or forest/shrub ecotones (Brenner, et al. 1992). The downy woodpecker uses tree and shrub foliage for cover; it also digs cavities for nesting and roosting in deciduous trees (Zeiner et al. 1990).
Biogeography
Downy woodpeckers are resident in appropriate habitats from western and central Alaska eastward to Newfoundland southward to southern California and southern Florida (AOU 1998). Some populations migrate or withdraw to southward areas from the northern part of the range in the fall and winter. Otherwise, the species tends to descend from the higher mountains to winter within lower elevation habitat (Terres 1980).
Zeiner, et al. (1990) summarize the distribution, abundance, and seasonality of the downy woodpecker within California as follows. It is a common, year-long resident of riparian deciduous and associated hardwood and conifer habitats. The downy woodpecker occurs throughout the state, usually below 1,800 meters (5,900 ft). It is absent from southern California desert regions. In southern California, the downy woodpecker is present from Los Angeles County southward and eastward locally through San Bernardino County and Riverside County, south to the vicinity of Temecula, and into northern San Diego County (Garrett and Dunn 1981). The species primarily occurs in the lowlands and foothills and is generally absent in mountainous areas but is known to occur within the montane regions in low numbers (Garrett and Dunn 1981).
Formerly termed locally common (Grinnell and Miller 1944), the downy woodpecker has been more recently noted in southern California as fairly common from Los Angeles or Ventura Counties northwards but extending uncommonly and very locally south to extreme northern San Diego County (Garrett and Dunn 1981).
Known Populations Within Western Riverside County
Downy woodpeckers are primarily confined to the northwestern and southwestern portions of the Plan Area according to Garrett and Dunn (1981). Core areas include the large concentration in the Prado Basin and contiguous reaches of the Santa Ana River. Other Core Areas include Temescal Wash, Alberhill Creek, Temecula Creek and Vail Lake.
Other geographic locations recorded within the U.C. Riverside database include: Lake Mathews, the UCR campus area west of Box Springs, Motte-Rimrock Reserve, San Jacinto River, the Badlands, Murrieta Hot Springs, Lake Skinner, Wilson Creek, Lake Perris, Potrero Creek, and San Timoteo Creek. The downy woodpecker has been recorded to be present at Murrieta Creek, and at Railroad Canyon (Michael Patten, Riverside County Editor for American Field Notes and Past Secretary, California Bird Records Committee, pers. comm., 1998). The downy woodpecker has been recorded in low numbers in the Cleveland National Forest and the San Bernardino National Forest and is documented to occur at these higher elevations in relatively low numbers (Garrett and Dunn 1981).
Biology
Genetics: Studies of mitchondrial DNA show little polymorphism between the downy woodpecker and mourning dove (Ball and Avise 1992). The study raises questions concerning currently-held evolutionary structures.
Diet and Foraging: Beetles, ants, caterpillars, and other larvae comprise 75-80 percent of the annual diet of the downy woodpecker. The species also eats cambium, berries and other fruits, nuts and seeds, including dogwood, serviceberry, and poison-oak. The downy woodpecker forages on trunks and branches of small trees, usually 2.7 to 20 meters (9-65 feet) above ground (Jackson 1970). It also forages in shrubs and occasionally tall herbs. The species probes, pecks, gleans for insects and occasionally hawks insects (Bent 1939).
Unlike some other woodpecker species, downy woodpeckers forage on a variety of foods over a large winter home range and do not re-visit cache locations (Volman, et al. 1997). Downy woodpeckers, among woodpeckers, appears to be a generalist in terms of excavation foraging where this species uses more tree species than other woodpeckers (Conner, et al. 1994). Downy woodpeckers also showed a preference of smaller diameter substrates (Conner, et al. 1994).
Daily Activity: As a cold-tolerant species, downy woodpeckers were found to have significantly higher basal and peak metabolic rates during winter than in summer (Linknes and Swanson 1996). Thus they are able to maintain activity in colder areas.
Reproduction: Within southern California, the downy woodpecker generally nests in deciduous (often willow) woodlands, deciduous oak woodlands, orchards, suburban plantings, and occasionally in conifers (Garrett and Dunn 1981). The species seems to prefer aspen for the nest cavity (possibly a softer wood) in areas where that tree species is present (Bent 1939). The downy woodpecker excavates a nest cavity in a snag or dead branch 1.3 to 15 meters (4-50 feet) above the ground. The downy woodpecker uses a nest tree that is at least 23 centimeters (9 inches) diameter breast high (Bent 1939, Lawrence 1967). It usually excavates a new nest cavity each year. This species is characterized as a relatively weak excavator therefore preferring to nest in dead trees or dead tops of live trees or to use extremely soft woods (Harestad and Keisker 1989).
As with most woodpeckers, courtship includes the male drumming on dry, resonant limbs to attract a female (Bendire 1895). Breeding occurs from late March to early September; with a peak nesting activity during May through June. The average clutch is 4-5 eggs; the range is 3-7 eggs. The duration of the incubation period is 12-13 days. Both parents incubate and care for the altricial young. Usually 1 brood is raised per year (Dawson 1923).
Survival: No information is available or was reviewed.
Dispersal: No information is available or was reviewed.
Socio-Spatial Behavior: During wintering, downy woodpeckers form a loose social structure where male-female associations may occur, and individuals are generally seen with two or three conspecifics but no evidence of territorial behavior or permanent pair bonds are observed (Matthysen, et al. 1993). Territory and home range apparently are the same for this species (Zeiner et al. 1990). In Ontario, Lawrence (1967) observed 2 downy woodpecker breeding territories of 2.0 and 3.2 hectares (5 and 9 acres). The downy woodpecker did not occur in small wood lots until the size of the woodlot reached 1.2 hectares (Forman et al. 1976).
Community Relationships: There is potential intraspecific competition for food between male and female downy woodpeckers which is apparently reduced by sexual differences in feeding behavior (Jackson 1970, Kilham 1970). Interspecific competition for food between hairy and downy woodpeckers may be reduced by feeding on different species of trees (Kisiel 1972). In Idaho, Ligon (1970) reported competition for food between white-headed and downy woodpeckers.
Threats to Species
The species has almost certainly declined overall due to ongoing destruction of woodland habitats within southern California (Zeiner et al. 1990). Loss of riparian woodlands and snags has caused a decline in numbers in recent decades (Grinnell and Miller 1944). No other threats have been identified within the literature.
Special Biological Considerations
The species requires abundant snags, and tree/shrub, tree/herbaceous, and shrub/herbaceous ecotones (Zeiner, et al. 1990). Abandoned snag and tree cavities are used by many other species, thus there is potential for a shortage of snags and tree cavities and resulting competition between species.
Artificial snags (polystyrene) have been placed in forests in an attempt to mimic natural snags. Downy woodpeckers are one of a few species which use the artificial snags for excavation and night roosting; however they do not use them for nesting (Conner and Saenz 1996).
Mechanical strip thinning of aspen is a method of harvesting found to be relatively compatible with both forest-dwelling mammals and birds, including downy woodpeckers (Christian and Hanowski 1996).
Supplementary feeding has been identified as a positive management technique for wintering populations of the downy woodpecker (Grubb and Cimprich 1990).
LITERATURE CITED
AOU (American Ornithologists' Union). 1998. Check-List of North American Birds. Seventh Edition. American Ornithologists' Union, Washington, D.C. 829 pp.
Austin, G. T. 1976. Sexual and seasonal differences in foraging of ladder-backed woodpeckers. Condor 78:317-323.
Ball, R. M. Jr. and J. C. Avise. 1992. Mitochondrial DNA phylogeographic differentiation among avian populations and the evolutionary significance of subspecies. Auk 109:626-636.
Bendire, C. 1895. Life histories of North American birds. Vol. 2. Smithsonian Contrib. to Knowledge No. 985. Smithsonian Inst., Washington DC. 518 pp.
Bent, A.C. 1939. Life histories of North American woodpeckers. U.S. Natl. Mus. Bull. 174. 334 pp.
Brenner, F. J., B.E. Fisher, and D. Laferrierre. 1992. Habitat use and differential foraging behavior in the downy woodpecker. Journal of the Pennsylvania Academy of Science 66: 15-17.
Christian, D. P., J. M. Hanowski, M. Reuvers-House, G. J. Niemi, J. G. Blake, W. E. Berguson. 1996. Effects of mechanical strip thinning of aspen on small mammals and breeding birds in northern Minnesota, U.S.A. Canadian Journal of Forest Research 26:1284-1294.
Conner, R. N. and D. Saenz. 1996. Woodpecker excavation and use of cavities in polystyrene snags. Wilson Bulletin 108: 449-456.
Conner, R. N., S. D. Jones and G. D. Jones. 1994. Snag condition and woodpecker foraging ecology in a bottomland hardwood forest. Wilson Bulletin 106:242-257.
Dawson, W.L. 1923. The birds of California. 4 Vols. South Moulton Co., San Diego, 2121 pp.
Forman, R. T. T., A. E. Galli, and C. F. Leck. 1976. Forest size and avian diversity in New Jersey woodlots with some land use implications. Oecologia (Berl.) 26: 1-8.
Garrett, K. and J. Dunn. 1981. Birds of Southern California: Status and Distribution. Los Angeles Audubon Society. 407 pp.
Grinnell, J. and A.H. Miller. 1944. The Distribution of the Birds of California. Pacific Coast Avifauna Number 27. Copper Ornithological Club, Berkeley, California. Reprinted by Artemisia Press, Lee Vining, California; April, 1986. 617 pp.
Grubb, T.C. and D. A. Cimprich. 1990. Supplementary food improves the nutritional condition of wintering woodland birds: Evidence from ptilochronology. Ornis Scandinavica 21:277-281.
Harestad, A. S. and D. G. Keisker. 1989. Nest tree use by primary cavity-nesting birds in south central British Columbia [Canada]. Canadian Journal of Zoology 67:1067-1073.
Jacson, J.A. 1970. A quantitative study of the foraging ecology of downy woodpeckers. Ecology 51:318-323.
Kilham, L. 1970. Feeding behavior of downy woodpeckers I. Preference for paper birches and sexual differences. Auk 87:544-556.
Kisiel, D.S. 1972. Foraging Behavior of Dendrocopos villosum and D. pubescens in eastern New York state. Confor 74:393-398.
Lawrence, L. de K. 1967. A comparative life-history study of four species of woodpeckers. Ornithol. Monogr. No. 5. 156 pp.
Ligon, J.D. 1970. Behavior and breeding biology of the red cockaded woodpecker. Aug 87:255-278.
Linknes, E. T. and D. L Swanson. 1996. Seasonal variation in cold tolerance, basal metabolic rate and maximal capacity for thermogenesis in white-breasted nuthatches and downy woodpeckers, two unrelated arboreal residents. Journal of Avian Biology 27: 279-288.
Matthysen, E., D. Cimprich, and T. C. Grubb Jr. 1993. Home ranges and social behaviour of the downy woodpecker in winter. Belgian Journal of Zoology 123:193-201.
Patten, Michael. 1998. Riverside County Editor for American Field Notes and Past Secretary, California Birds Records Committee, pers. comm.
Shackelford, C. E. and R. N. Conner. 1997. Woodpecker abundance and habitat use in three forest types in eastern Texas. Wilson Bulletin 109:614-629.
Stark et al. 1998. A quantitative analysis of woodpecker drumming. Condor 100: 350-356.
Terres, J. K. 1980. The Audubon Society Encyclopedia of North American Birds. Alfred A. Knopf, New York, New York. 1109pp.
Volman, S. F., T. C. Grubb Jr. and K. C. Schuett. 1997. Relative hippocampal volume in relation to food-storing behavior in four species of woodpeckers. Brain Behavior and Evolution 49:110-120.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
ferruginous hawk (Buteo regalis)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
ferruginous hawk (Buteo regalis)
Status:
State: Species of Special Concern
Federal: Federal Special Concern species; Partners in Flight Priority Bird Species; Species of Management Concern
Other: Audubon Society California Watch List
GROUP DESIGNATION AND RATIONALE
Group 1
The ferruginous hawk has a widespread distribution throughout the MSHCP Plan Area within suitable foraging habitat. It occurs within the Plan Area as a transient in the spring and fall and may winter within the area. It does not require specific conditions or locations for nesting because it does not nest in the region. It is an opportunistic predator that may forage anywhere within open habitats in the area.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include with the MSHCP Conservation Area at least 144,120 acres of agriculture (field crops), grassland, cismontane alkali marsh, playa and vernal pool, Riversidean alluvial fan sage scrub, coastal sage scrub, desert scrub, peninsular juniper woodland and scrub, and riparian scrub, woodland, and forest, including 2,690 acres at Mystic Lake/San Jacinto Wildlife Area and 5,520 acres of riparian habitat at Prado Basin/Santa Ana River.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
The ferruginous hawk uses predominantly open land including grassland for foraging as well as a wide variety of other habitats, including shrub and scrub habitats (Garrett and Dunn 1981). The ferruginous hawk winters and migrates throughout the MSHCP Plan Area. For the purpose of the conservation analysis, potential habitat for the ferruginous hawk includes agriculture (field crops), grassland, cismontane alkali marsh, playa and vernal pool, Riversidean alluvial fan sage scrub, coastal sage scrub, desert scrub, peninsular juniper woodland and scrub, and riparian scrub, woodland, and forest. The riparian and juniper woodland habitat is included because the species will use the trees in these habitats for roosting and as hunting perches. The scrub habitats are included because they have been recorded hunting within sparse forms of such habitats. The other habitats included above comprise open habitat within which they typically forage. Based on these habitats, the Plan Area supports approximately 401,410 acres of potential habitat for the ferruginous hawk. Table 1 shows the conservation and loss of potential habitat for the ferruginous hawk. Overall, approximately 144,120 acres (36 percent) of potential habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public Lands.
As described below under Data Characterization, 25 of the 60 recent point localities have a high location precision. Of these 25 point localities, 8 will be inside the criteria area or public/quasi-public lands. A total of 17 point localities will be outside of the MSHCP Conservation Area. Conservation of this species should be considered from a landscape perspective because the species is found throughout the Plan Area and may occur in a variety of habitats. The main areas within which the species has been observed, Prado Basin/Santa Ana River (including 5,520 acres of riparian habitat within the MSHCP Conservation Area) and Mystic Lake/San Jacinto Wildlife Area (including 2,690 acres of suitable habitat), will be conserved. While there are definable locations for focusing conservation efforts, there do not appear to be Core Areas that will be essential for conservation of the species.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
FERRUGINOUS HAWK
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| Riverside Lowlands and San Jacinto Foothills Bioregions | |||||||
| Agriculture (field crops) | 117,870 | 6,930 | 9,850 | 16,780 | 710 | 100,380 | 101,090 |
| Grassland | 121,750 | 17,470 | 16,130 | 33,600 | 7,000 | 81,150 | 88,150 |
| Cismontane Alkali Marsh | 10 | 10 | 0 | 10 | 0 | 0 | 0 |
| Playas and Vernal Pools | 7,870 | 3,830 | 2,880 | 6,710 | 0 | 1,160 | 1,160 |
| Riversidean Alluvial Fan Sage Scrub | 5,430 | 2,710 | 1,310 | 4,020 | 160 | 1,250 | 1,410 |
| Coastal Sage Scrub | 133,110 | 43,690 | 27,200 | 70,890 | 19,740 | 42,480 | 62,220 |
| Desert Scrubs | 2,230 | 2,160 | 0 | 2,160 | 40 | 30 | 70 |
| Peninsular Juniper Woodland and Scrub | 930 | 340 | 180 | 520 | 0 | 410 | 410 |
| Riparian Scrub, Woodland, Forest | 12,210 | 3,570 | 5,860 | 9,430 | 180 | 2,600 | 2,780 |
| TOTAL | 401,410 | 80,710 (20%) |
63,410 (16%) |
144,120 (36%) |
27,830 (7%) |
229,460 (57%) |
257,290 (64%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
MSHCP Conservation Area Configuration Issues
Several large blocks of habitat supporting the current known and potential foraging locations of the ferruginous hawk will be conserved as Criteria Area and Public/Quasi-Public including the Prado Basin, Santa Ana River, Lake Mathews-Estelle Mountain, Vail Lake/Wilson Valley, Lake Skinner/ Diamond Valley Lake, Mystic Lake/San Jacinto Wildlife Area and surrounding playa habitat, and the Badlands. Additional areas that provide potential foraging habitat include Sycamore Canyon Regional Park, Lake Elsinore grassland area, Sedco Hills, Box Springs Mountain, Lakeview Mountains, Sage, and foothills of the National Forest lands. As identified above, the species occurs within the MSHCP Plan Area as a transient migrant and wintering resident and as such, the MSHCP Conservation Area will provide adequate habitat for foraging and perch sites. These MSHCP Conservation Area areas are linked as well, however the ferruginous hawk, due to its ability to move long distances, may rely less on the linkage than other species.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 144,120 acres of suitable Conserved Habitat including agriculture (field crops), grassland, cismontane alkali marsh, playa and vernal pool, Riversidean alluvial fan sage scrub, coastal sage scrub, desert scrub, peninsular juniper woodland and scrub, and riparian scrub, woodland, and forest. The main areas within which the species has been observed, Prado Basin/Santa Ana River and Mystic Lake/San Jacinto Wildlife Area, will be conserved in the MSHCP Conservation Area. The current population size of the ferruginous hawk is unknown, however the foraging habitat requirements are well defined. The species is moderately predictable in its occurrence and may vary in number within the area from a few to many individuals. It has occurred repeatedly in a number of conserved locations.
INCIDENTAL TAKE
About 257,290 acres (64 percent) of potential habitat for the ferruginous hawk will be outside the Criteria Area and Public/Quasi-Public designations and individuals occurring within these areas will be subject to Incidental Take consistent with the Plan.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The location database for the ferruginous hawk includes approximately 90 data records from 1900 to 1999. Of these records, approximately 60 are relatively recent (within the past 10 years) and of these 25 are of high precision and may be accurately located within the Plan Area. Approximately five of these high precision records are located within developed areas and although they may no longer exist, they may also represent a wintering or transient bird hunting within a residential area. The rest occur within non-native grassland, alkali playa, riparian, sage scrub, chaparral, field crop lands and other vegetation communities that are likely occupied by the species for foraging during its transient and wintering movements throughout the Plan Area.
A moderate amount of literature is available for the ferruginous hawk because it is a bird of prey and is of generally high interest to the ornithological audience. Most of the literature pertains to general natural history, niche determination, and the buteos in general. Few controlled scientific studies have been conducted; however, some management studies are available. Very little information is available for the Plan Area other than what is available regarding basic distribution information.
Habitat and Habitat Associations
The ferruginous hawk is an occupant of open dry country and will perch on badger mounds or hillocks when trees or posts are not available. It requires large, open tracts of grasslands, sparse shrub, or desert habitats with elevated structures for nesting. Its wintering habitat is similar in being open and it may also occur in areas of mixed grassy glades and pineries (Brown and Amadon 1968).
Range-wide, within California, ferruginous hawks winter in open terrain and grasslands of plains and foothills (Grinnell and Miller 1944). Within southern California, including the Plan Area, ferruginous hawks typically winter in open fields, grasslands, and agricultural areas (Garrett and Dunn 1981). It frequents open grasslands, sagebrush flats, desert scrub, low foothills surrounding valleys, and fringes of pinyon-juniper habitats (Zeiner, et al. 1990). It searches for prey from low flights over open, treeless areas, and glides to intercept prey on the ground. It also hovers, and hunts from high mound perches. The ferruginous hawk roosts in open areas, usually in a lone tree or utility pole. It is tolerant of heat; the nest is often unshaded. There are no breeding records from California. The ferruginous hawk nests in foothills or prairies; on low cliffs, buttes, cut banks, shrubs, trees, or in other elevated structures (Zeiner, et al. 1990).
Biogeography
The ferruginous hawk breeds from British Columbia locally eastward to southwestern Manitoba generally southward to Nevada and Texas. The species winters from central and southern parts of the breeding range southward to Baja California and northern mainland Mexico (AOU 1998).
The ferruginous hawk broadly occupies areas where it was reported in historically. Its range has retracted at the edge in Alberta, Saskatchewan, and Manitoba during the early 1900s owing to agriculture and invasion of aspen into remaining prairie habitats. Historically, the ferruginous hawk wintered in the Los Angeles area. Christmas Bird Count data show increases in birds wintering in the eastern portion of the range and in California during the 1980s owing to loss of wintering habitat in the Great Plains (Bechard and Schmutz 1995).
It does not breed in southern California but winters there in interior and coastal areas (Garrett and Dunn 1981). Zeiner, et al. (1990) describe the distribution, abundance, and seasonality of the ferruginous hawk as follows. It is an uncommon winter resident and migrant at lower elevations and open grasslands in the Modoc Plateau, Central Valley, and Coast Ranges. The ferruginous hawk is a fairly common winter resident of grasslands and agricultural areas in southwestern California (Garrett and Dunn 1981). It is casual in the northeast in summer. It is migratory; it generally arrives in California in September and departs by mid-April.
Known Populations Within Western Riverside County
Ferruginous hawks may be found locally in appropriate habitats nearly throughout western Riverside County, which is an important wintering area for this species, especially within the central portion of the Plan Area.
Important wintering areas in southern California as a whole include the Lakeview-Perris area (Garrett and Dunn 1981). Elsewhere, ferruginous hawk habitats occur in the Prado Basin, the Badlands, the Temecula/Murrieta area, Diamond Valley Lake, and Rawson Canyon and environs (Michael Patten, Riverside County Editor for American Field Notes and Past Secretary, California Bird Records Committee, pers. comm., 1998).
Biology
Genetics: No subspecies have been recognized for the ferruginous hawk. The historic nomenclature includes numerous abandoned synonyms. Chromosomes in the ferruginous hawk were found to be similar in shape and number to those in the gray hawk, red-tailed hawk, rough-legged hawk, white-tailed hawk, roadside hawk, and Harris' hawk. The chromosomes of the ferruginous hawk were found to be different in shape from the Swainson's hawk and broad-winged hawk (Bechard and Schmutz 1995).
Diet and Foraging: Cooperative hunting and ground pursuit of prey have been observed in the ferruginous hawk. The species searches for prey from low flights over open, treeless areas, and glides to intercept prey on the ground. The species also hovers and hunts from high mound perches. It mostly eats lagomorphs, ground squirrels, and mice; it also takes birds, reptiles, and amphibians. Population trends may follow lagomorph population cycles. Ground squirrels, jackrabbits or cottontail rabbits may be an important component of this species' diet (Grinnell and Miller 1944; Bechard and Schmutz 1995).
Daily Activity: The ferruginous hawk roosts in open areas usually in a lone tree or utility pole (Zeiner, et al., 1990). When prey is abundant, hunting occurs from daybreak to mid-morning, then again from late afternoon and evening (Bechard and Schmutz 1995). In winter, these hawks spend most of the day perched (Bechard and Schmutz 1995; Plumpton and Andersen 1997). In hot weather, it often hunts only in early morning and late afternoon (Zeiner, et al. 1990).
Reproduction: The ferruginous hawk nests in foothills or prairies; on low cliffs, buttes, cut banks, shrubs, trees, or in other elevated structures, natural or human-made (Bent 1937, Olendorff 1973, Call 1978). The nest tree is often isolated, or in a transition zone to an adjacent community (Smith and Murphy 1973). Sticks up to 2.5 centimeters (1 inch) are used to construct the nest; dried manure may also be used (Olendorff 1973, Call 1978). Ferruginous hawks are monogamous (Bechard and Schmutz 1995). Nesting occurs primarily in trees and shrubs (49 percent), followed by cliffs (21 percent), utility structures (12 percent) and ground outcrops (10 percent) (Bechard and Schmutz 1995). A study in northwestern New Mexico found these hawks to most commonly nest on clay or rock pinnacles (53.9 percent) (Ramakka and Woyewodzic 1993). Average clutch size ranges from 2 to 4 eggs but it can range from 1 to 8 depending on prey abundance, with a mean number of fledglings per breeding pair per year at 2.9 (Bechard and Schmutz 1995). Other estimates show that only 42 percent of occupied nests produce fledglings and that the average successful nest produced 2.3 fledglings (Zelenak and Rotella 1997). Egg laying begins in April (Weston 1969, Olendorff 1973). It incubates about 28 days. The young fledge at 38-50 days (Olendorff 1973, Smith and Murphy 1973).
Survival: Banding information on the ferruginous hawk from the 1970s to 1980s suggests a first year mortality rate of about 65 percent, although this has been now thought to be an overestimate. Other estimates of adult mortality are approximately 25 percent. Maximum potential longevity is 20 years (Bechard and Schmutz 1995).
Dispersal: Dispersal of the ferruginous hawk after fledging may vary from 25 kilometers to as far as 1,700 kilometers. Little is known about fidelity to the winter home range by migratory individuals (Bechard and Schmutz 1995).
Socio-Spatial Behavior: For the ferruginous hawk, the average nearest-neighbor distances for several U.S. sites was 13.4 kilometers (Bechard and Schmutz 1995). In winter, several birds may perch within 50 meters of each other (Bechard and Schmutz 1995). Home ranges for the species were estimated at 5.9 km2 and 7.6 km2, with the latter area for breeding males (Bechard and Schmutz 1995). In South Dakota, home ranges were estimated to be 17-117 km2 (Zeiner et al. 1990).
Community Relationships: The ferruginous hawk tends to displace red-tailed and Swainson's hawks. The young may be preyed upon by golden eagles and great horned owls. It competes with the numerous avian and mammal species that prey upon small mammals.
Threats to Species
Continuing threats to the ferruginous hawk apparently include habitat destruction and fragmentation. In nearby Orange County, habitat destruction has occurred to the point that there is only habitat for about 10 birds per year (Hamilton and Willick 1996). Given its aforementioned attributes, the habitat of the ferruginous hawk is easily converted to other landscapes and human uses. Artificial disturbances, created to mimic land development, caused 33 percent of disturbed nests to be deserted and fledging success to be significantly lower compared to undisturbed nests. A minimum buffer zone of 0.25 kilometers around nests should be sufficient to prevent nest desertion if intermittent or brief human disturbance is necessary (White and Thurow 1985). Cultivation of habitat is thought to be the major threat to the species with lesser threats being grazing, poisoning and controlling small mammals, mining and fire (Bechard and Schmutz 1995).
Special Biological Considerations
Grinnell and Miller (1944) suggested that habitats selected by the ferruginous generally include a source of adequate prey, which may be especially ground squirrels. The ferruginous hawk requires large expanses of open ground. Artificial nest platforms may help increase populations where trees have died and fallen and in areas which have been converted to grass/shrub habitats (Bechard and Schmutz 1995). This species, along with other raptors, has been shown to exist compatibly in urban open space grasslands, as long as prey populations persist (Berry, et al. 1998).
Although area-wide surveys of the species have not been done, the species might be expected in appropriate habitats nearly throughout. In winter, the species is behaviorally flexible and tolerant of human disturbance and alteration of landscapes providing that an adequate prey base is available (Plumpton and Anderson 1997).
LITERATURE CITED
AOU (American Ornithologists' Union). 1998. Check-List of North American Birds. Seventh Edition. American Ornithologists' Union, Washington, D.C. 829 pp.
Bechard, M. J. and J. K. Schmutz. 1995. Ferruginous hawk (Buteo regalis). In The Birds of North America, No. 172 (A. Poole and F. Gill, eds.). The Academy of Natural Sciences, Philadelphia, PA and The American Ornithologists' Union, Washington, D.C.
Bent, A. C. 1937. Life histories of North American birds of prey. Part 1. U.S. Natl. Mus. Bull. 167. 409pp.
Berry, Mark E., Carl E. Bock and Sandra L. Haire. 1998. Abundance of diurnal raptors on open space grasslands in an urbanized landscape. Condor 100: 601-608.
Brown, L., and D. Amadon. 1968. Eagles, hawks and falcons of the world. 2 Vols. Country Life Books, London. 945pp.
Call, M. W. 1978. Nesting habits and survey techniques for common western raptors. U. S. Dep. Inter., Bur. Land Manage, Portland, OR. Tech. Note No. 316. 115pp.
Garrett, K. and J. Dunn. 1981. Birds of Southern California: Status and Distribution. Los Angeles Audubon Society. 407 pp.
Grinnell, J. and A.H. Miller. 1944. The Distribution of the Birds of California. Pacific Coast Avifauna Number 27. Copper Ornithological Club, Berkeley, California. Reprinted by Artemisia Press, Lee Vining, California; April, 1986. 617 pp.
Hamilton, R. and D.R. Willick. 1996. The Birds of Orange County, California: Status and Distribution. Sea and Sage Press, Irvine, California. 150 pp. with appendices.
Olendorff, R. R. 1973. The ecology of the nesting birds of prey of northeastern Colorado. U.S. Dep. Inter. Natl. Res. Ecol. La., Colorado State Univ., Fort Collins. Biol. Prog. Tech. Rep. No. 211. 233pp.
Patten, Michael. 1998. Riverside County Editor for American Field Notes and Past Secretary, California Bird Records Committee, pers. comm.
Plumpton, D.L. and D.E. Andersen. 1997. Habitat use and time budgeting by wintering ferruginous hawks. Condor 99:888-893.
Ramakka, J. M. and R. T. Woyewodzic. 1993. Nesting Ecology of Ferruginous Hawk in Northwestern New Mexico. Journal of Raptor Research 27:97-101.
Smith, D. G., and J. R. Murphy. 1973. Breeding ecology of raptors in the eastern Great Basin of Utah. Brigham Young Univ., Provo. Sci. Bull. Biol. Ser. 18, No. 3. 76pp.
Weston, J. B. 1969. Nesting ecology of the ferruginous hawk, Buteo regalis. Brigham Young Univ., Provo, UT. Sci. Bull. Biol. Ser. 10:25-36.
White, C. M. and T. L. Thurow. 1985. Reproduction of ferruginous hawks (Buteo regalis) exposed to controlled disturbances. Condor 87:14-22.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
Zelenak, J. R. and J. J. Rotella. 1997. Nest success and productivity of Ferruginous Hawks in northern Montana. Canadian Journal of Zoology 75:1035-1041.
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
golden eagle (Aquila chrysaetos)
Status:
State: Species of Special Concern, and Fully Protected Species
Federal: Partners in Flight Priority Bird Species; San Bernardino National Forest Sensitive
GROUP DESIGNATION AND RATIONALE
Group 2
The golden eagle is widely distributed as a foraging species throughout the MSHCP Plan Area within all bioregions and in virtually all habitats except dense conifer woodlands at high elevations. There are several golden eagle nest sites within the Plan Area as well. Nest sites occur within a variety of habitats, predominantly chaparral, but are more closely associated with specific topography and micro-habitat features than habitat type. Nest site locations include Temecula Gorge, in the hills east of Sun City, in the hills north of Aguanga west of State Route 371, Elsinore Peak, Rawson Canyon, Double Butte, Mesa de Burro on the Santa Rosa Plateau, on a transmission line in San Timoteo Canyon (likely nest) and possibly in the Box Springs Mountains and on Arlington Mountain, although these last two locations may have now been abandoned. These nest site locations will be considered core areas that require conservation.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 164,390 acres of suitable foraging habitat for the golden eagle including grasslands, playas and vernal pools, desert scrubs, Riversidean alluvial fan sage scrub, oak woodlands and forests, and coastal sage scrub. Conserved habitats will be distributed throughout all bioregions of the Plan Area.
Objective 2
Include within the MSHCP Conservation Area and buffer from disturbance the known nesting locations at Temecula Gorge, in the hills north of Aguanga west of State Route 371, at Elsinore Peak, at Rawson Canyon, at Mesa de Burro on Santa Rosa Plateau, and in San Timoteo Canyon (likely nest). Buffering of the nest sites will include conservation of undeveloped habitat in the MSHCP Conservation Area within a one mile radius around each of the nest site locations and may include a variety of habitats.
Objective 3
Maintain (once every 8 years) the continued use of, and successful reproduction at 75 percent of the known nesting localities (including any nesting locations identified in the MSHCP Conservation Area in the future). Successful reproduction is defined as a nest which fledged at least one known young.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
The golden eagle uses predominantly sparse woodland or forest, rocky cliff or slope, brushy, scrubby, or grassy habitats for nesting and foraging (Garrett and Dunn 1981). Other observations, within agriculture and developed areas may constitute winter foraging areas by the resident population or migrants that move into the Plan Area for the winter and observations within chaparral habitat generally constitute use of a sparse form of that vegetation community (Garrett and Dunn 1981). The golden eagle, as a resident and winter migrant, has been recorded virtually throughout the MSHCP Plan Area except in the high elevation densely forested areas. The golden eagle also breeds at several locations in the Plan Area. For the purpose of the conservation analysis, potential habitat for the golden eagle includes the habitat where the required cliff sites for breeding occur and suitable foraging habitat including woodlands and forests, coastal sage scrub, desert scrubs, Riversidean alluvial fan sage scrub, grassland, and playa and vernal pool. Agriculture land has not been included at the request of the USFWS and also because, although the species may use these areas periodically, the literature indicates that usage is predominantly within the non-breeding season (Cleary-Rose 2002 pers. comm.; Garrett and Dunn 1981). Chaparral habitat has not been included within the analysis, although most of the nest sites are located within areas that are mapped as chaparral, because much of the chaparral habitat may be too dense to provide suitable foraging habitat and the characteristics of the nest site are more important than the habitat within which the nest site is located (LaPré 2002). Based on these habitats, the Plan Area supports approximately 356,160 acres of potential habitat for the golden eagle. Table 1 shows the conservation and loss of potential habitat for the golden eagle. Overall, approximately 164,390 acres (46 percent) of potential habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public lands. In addition, although not included in Table 1, a total of 272,270 acres (66%) of chaparral and 20,020 acres (12%) of agriculture lands will be conserved in Criteria Area or existing Public/Quasi-Public lands. Golden eagles forage within chaparral vegetation predominantly when it is relatively sparse in shrub cover. The Plan Area has not been mapped to distinguish between sparse and dense chaparral, thus this plant community is not included within the table. The acreage numbers listed above include both types of chaparral and indicate that some chaparral is preserved within Criteria Area and Public/Quasi-Public Lands. Management actions will be incorporated into the conservation strategy so that activities near nesting sites will be compatible with golden eagle nesting activities.
This species occurs within the Forest Service lands as well as the lowland bioregions as a breeding and foraging species. It occurs predominantly within grasslands, sparse deciduous woodland, sparse chaparral, and coastal sage scrub. Under the existing Forest Land allocation plan, these locations and habitats generally are located within the San Jacinto and San Mateo Canyon wilderness areas, the roadless areas, and in most of the grazing allotments as well. The golden eagle has been documented to have a nest site at Elsinore Peak which is in the San Mateo Canyon Wilderness Area. It also occurs within the San Bernardino National Forest although nesting locations have not been documented either due to low survey effort or lack of reporting. Conservation of a one mile radius around the nest site at Elsinore Peak is an important conservation method for this species for the Forest Service.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
GOLDEN EAGLE
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| Grassland | 146,870 | 20,010 | 22,810 | 42,820 | 12,220 | 91,830 | 104,050 |
| Playas and Vernal Pools | 7,910 | 3,830 | 2,920 | 6,750 | 0 | 1,160 | 1,160 |
| Desert Scrubs | 9,360 | 3,670 | 1,310 | 4,980 | 40 | 4,340 | 4,380 |
| Riversidean Alluvial Fan Sage Scrub | 7,150 | 3,170 | 2,060 | 5,230 | 220 | 1,700 | 1,920 |
| Oak Woodlands and Forests | 32,180 | 2,390 | 20,500 | 22,890 | 5,020 | 4,270 | 9,290 |
| Coastal Sage Scrub | 152,690 | 47,160 | 34,560 | 81,720 | 26,240 | 44,730 | 70,970 |
| Chaparral | 413,470 | 64,900 | 207,370 | 272,270 | 59,580 | 81,620 | 141,200 |
| TOTAL | 769,630 | 145,130 (19%) |
291,530 (38%) |
436,660 (57%) |
103,320 (13%) |
229,650 (30%) |
332,970 (43%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
Conservation of this species will be considered from a combination of site specific location and landscape perspective because the species requires a very specific nest location as well as a more general area for foraging habitat. As described below under Data Characterization, 46 of the 124 recent point localities have a high location precision. Of these 46 point localities, 14 will be inside the Criteria Area or Public/Quasi-Public Lands. Four point locations are located within the Rural/Mountainous category. A total of 28 point localities will be outside of the MSHCP Conservation Area. These point localities represent general records and do not identify the type or activity of the observation (e.g., nest, pair, foraging, flight, etc.). Of greater interest for site specific conservation analysis than the general locality records described above are the locations of nest sites. Nest site locations include Temecula Gorge, in the hills north of Aguanga west of State Route 371, Elsinore peak, Rawson Canyon, Mesa de Burro on Santa Rosa Plateau, in San Timoteo Canyon near El Casco (likely nest), Double Butte, in the hills east of Sun City, possibly in the Box Springs Mountains, and on Arlington Mountain, although these last three sites may now be abandoned. The currently active nest site locations will be considered core areas that require analysis for conservation. Although all known nest sites are important because of the historic, traditional, and repeated use by this species (Palmer 1988; LaPré 2002), conditions have changed within the Plan Area that appear to have made some nest site locations unsuitable and thus these locations will not be analyzed. Additionally conservation of nest sites will include preservation of habitat around the nest. A correlation between extant and abandoned nest sites indicates that a 1.6 kilometer (1 mile) radius with no human disturbance is significant as discussed below. Thus, each of the conserved nest sites, to be considered conserved will have a 1.6 kilometer (1 mile) buffer of no new human residences. The nest sites at Temecula Gorge, in the hills north of Aguanga west of State Route 371, Elsinore peak, Rawson Canyon, Mesa de Burro, and the likely nest site at San Timoteo Canyon are conserved and currently have a buffer around them of Public/Quasi-Public and/or Criteria Area designations. One site, Elsinore Peak is within the Cleveland National Forest in the San Mateo Canyon Wilderness area and will rely on conservation by the Forest Service.
Finally, as identified in Objective 3, the MSHCP Conservation Area will maintain (once every 8 years) the continued use of, and successful reproduction at 75 percent of the known golden eagle known nesting localities (including nesting locations identified in the MSHCP Conservation Area in the future). Successful reproduction is defined as a nest which fledged at least one known young.
Rural/Mountainous Designation Areas
As depicted on the MSHCP map (Figure 3-1, MSHCP Volume 1), certain areas adjacent to or in proximity to the MSHCP Conservation Area are designated as Rural/Mountainous in the County's General Plan. These areas are generally constrained for development due to steep topography and the level of development in these areas is anticipated to be of a low density, rural residential character. While these areas will not be included within the MSHCP Conservation Area or managed for the benefit of species conserved under the MSHCP, the low levels of development anticipated in these areas could provide a buffer to the edge of the MSHCP Conservation Area. For the golden eagle, the Rural/Mountainous designations may provide foraging opportunities and may allow the movement of prey species to and from the larger blocks of MSHCP Conservation Area within areas including, but not limited to, the Santa Rosa Plateau, Badlands, and Sage area.
MSHCP Conservation Area Configuration Issues
Several large blocks of habitat supporting the current known and potential foraging and nesting locations of the golden eagle will be conserved within the MSHCP Conservation Area including the nest sites at Elsinore Peak, Temecula Gorge, Aguanga, Mesa de Burro, San Timoteo Canyon (likely nest) and Rawson Canyon. The nest sites at Elsinore Peak, Temecula Gorge, Mesa de Burro, and Rawson Canyon are within Public/Quasi-Public designations with the buffer distance as specified in Objective 2. The nest sites at San Timoteo Canyon and Aguanga are within Criteria Area and also have the buffer distance as specified in Objective 2 composed of both Criteria Area and Public/Quasi-Public designations. Additional locations which may contain potential nesting areas and contain potential and known foraging habitat include the Badlands, Lake Perris and environs, Lake Mathews-Estelle Mountain, Alberhill/Meadowbrook, Cactus Valley, the Prado Basin, Beauty Mountain area, and sparsely forested areas within the Cleveland and San Bernardino national forests. These areas also contain the potential to provide the buffer distance identified in Objective 2. Adequate foraging areas also are provided with the MSHCP Conservation Area configuration. As identified below, the golden eagle requires a large area to support the nest site and has been estimated for southern California to be approximately 36 square miles (Dixon 1937). The nest site at Elsinore Peak is within a large block of the Cleveland National Forest. The Temecula Gorge nest site is located within the large block of habitat in Existing Core G and also is contiguous with conserved areas south within San Diego County. The Aguanga nest site is within the large block of Proposed Core 7 but is also near the Existing Cores M and L. The Mesa de Burro nest site is within the large block of habitat in Existing Core F and is linked to the Cleveland National Forest by the Proposed Linkage 9. The likely San Timoteo Canyon nest site is located within the Proposed Core 3 and may also use the Proposed Linkage 12. The Rawson Canyon nest site is within the Existing Core J and may use the habitat within the Proposed Extensions of Existing Core 5, 6, and 7 as well as habitat within Proposed Cores 4 and 7 which are linked by Proposed Linkages 13 and 14. As identified above, the species occurs within the MSHCP Plan Area as a breeding and wintering resident and as such, the MSHCP Conservation Area will provide adequate habitat for nesting and foraging.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 164,390 acres of suitable Conserved Habitat, the known nest sites at Temecula Gorge, in the hills north of Aguanga west of State Route 371, at Elsinore Peak, on Mesa de Burro on the Santa Rosa Plateau, in San Timoteo Canyon near El Casco (likely nest), and in Rawson Canyon, and the 1 mile buffer protection around the nest sites, as described above. The current population size of the golden eagle is unknown however there are recorded nesting locations. As identified in Objective 3, the MSHCP Conservation Area will maintain (once every 8 years) the continued use of, and successful reproduction at 75 percent of the known golden eagle known nesting localities (including any nesting locations identified in the MSHCP Conservation Area in the future). Although the Sun City, Arlington Mountain, Box Springs Mountains (potential), and Double Butte nesting locations are not included within the MSHCP Conservation Area, they have not been recently documented as being active and no take of active nest sites will be permitted.
INCIDENTAL TAKE
About 191,770 acres (54 percent) of potential habitat for the golden eagle will be outside the Criteria Area or Public/Quasi-Public designations, and will be subject to Incidental Take consistent with the Plan. Of this, approximately 43,740 acres (12 percent) of potential habitat are located within Rural/Mountainous designation areas. While the Rural/Mountainous areas are not included within the MSHCP Conservation Area and will not be managed for the benefit of wildlife, the anticipated levels of development in these areas will likely be consistent with maintaining some habitat for foraging for the golden eagle. Four point locations are located within the Rural/Mountainous category. A total of 28 point localities will be outside of the MSHCP Conservation Area. The nest site location at Double Butte is not considered conserved and has not been documented as being active. The nest site location in the hills east of Sun City is within the Rural/Mountainous designation. The current status of the Sun City site is not known. The CNDDB recorded it as active in 1993. It was not mentioned as being active during recent discussions of nest sites (P. Bloom 2001 pers. comm.). The two known or potential nest site locations in the Box Springs Mountains and on Arlington Mountain are no longer active (LaPré 2002). No take of active nest sites will be permitted.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The UCR location database includes approximately 176 location records dated from 1905 to 1999 with approximately 25 records containing no date. Most of the UCR database records are likely observation of the birds in flight. Approximately 124 of the records are dated within the relatively recent period (within the past 10 years) and approximately 46 of these are precisely located. Because most of the records are likely to be observations of birds in flight, even the habitats recorded as residential for the record may be extant and may coincide with an overflight. The UCR database confirms that the species is present within the Plan Area, uses essentially the entire Plan Area and uses a wide variety of habitats. There are a few breeding location records within the UCR database however, most are either very old, are not dated, and are not mapped with a suitable degree of accuracy. Nest location information was gathered from other sources. Three recent records are within the CNDDB database for 1993: Temecula Gorge, in the hills east of Sun City, and the hills north of Aguanga west of State Route 371. These are may be still active or still suitable, however breeding activity has not been confirmed or mentioned in recent communications. Additional records are also reported for Elsinore Peak, Rawson Canyon, and possibly Double Butte (P. Bloom 2001 pers. comm.) and Mesa de Burro on the Santa Rosa Plateau, on a transmission line in San Timoteo Canyon near El Casco (likely nest) and possibly in the Box Springs Mountains and on Arlington Mountain although these last two locations appear to now be abandoned (Tierra Madre Consultants, Inc. 1999; LaPré 2002).
There is a relatively large amount of literature available on the golden eagle within the scientific literature. The golden eagle, as a bird of prey, is a species of interest to ornithologists, is easily observed and has been well documented as to its habitat needs and reproductive strategy. A number of university theses and agency technical reports have been devoted to this species due to its overall high profile. Nonetheless, there is little information directly related to the species within the Plan Area.
Habitat and Habitat Associations
Range-wide, golden eagles occur locally in open country (e.g., tundra, open coniferous forest, desert, barren areas), especially in hills and mountainous regions (AOU 1998). Within southern California, the species prefers grasslands, brushlands (coastal sage scrub and sparse chaparral), deserts, oak savannas, open coniferous forests, and montane valleys (Garrett and Dunn 1981). It uses rolling foothills and mountain terrain, wide arid plateaus deeply cut by streams and canyons, open mountain slopes, and cliffs and rock outcrops. Habitat for the golden eagle is typically rolling foothills, mountain areas, sage-juniper flats, and desert within its range in California (Zeiner, et al. 1990). The species requires a large expanse for foraging and suitable nest sites in the form of cliffs or large trees. Nesting is primarily restricted to rugged, mountainous country (Garrett and Dunn 1981). Secluded cliffs with overhanging ledges and large trees are used for cover (Zeiner, et al. 1990). Thus, the golden eagle uses a variety of habitats, nesting in cliffs or trees and rugged terrain and foraging over plains, grasslands, or low and open shrublands including chaparral and coastal sage scrub (Scott 1985).
Golden eagles typically are not found in heavily forested areas or on the immediate coast and are almost never detected in urbanized environments (e.g., Grinnell and Miller 1944; Garrett and Dunn 1981).
Biogeography
The golden eagle has a holarctic distribution, extending as far south as north Africa, Arabia, and the Himalayas in the Old World, and Mexico in North America. It is a partial migrant within this distribution, with the northern breeding birds migrating south in winter, while those of more temperate climates remain all the year round (Brown and Amadon 1968). Golden eagles in North America breed locally from northern Alaska eastward to Labrador southward to northern Baja California, northern Mexico, and Maine. The species winters from southern Alaska and southern Canada southward through the breeding range.
Within California the golden eagle is described as an uncommon permanent resident and migrant throughout California, except the center of the Central Valley. It may be more common in southern California than in northern regions. It ranges from sea level up to 3833 meters (0-11,500 feet) (Grinnell and Miller 1944). Golden eagles are sparsely distributed throughout most of California, occupying primarily mountain and desert habitats. Approximately 500 breeding pairs are estimated to nest in California. They are mostly resident, but may move downslope for the winter, or upslope after the breeding season. Some individuals migrate into California for the winter (Zeiner, et al. 1990).
Known Populations Within Western Riverside County
The species apparently occurs (or has occurred) locally throughout much of western Riverside County in suitable habitats. The U.C. Riverside database indicates the species has been reported generally throughout the Plan Area except within the high elevation heavily forested portions of the eastern and western sections. Although area-wide surveys of the species have not been done in much of the Plan Area, the species could be present (in small numbers) in suitable habitats nearly throughout. The golden eagle is generally recorded throughout the central portion and foothill areas of the Plan Area. They have been recorded in the mountainous areas in very low numbers and probably are present but not recorded.
Nesting locations are sparse and most of them are old or undated. The species nested in 1998 in the Chino Hills just outside of the Plan Area. Current nesting locations include three recent records within the CNDDB database for 1993: Temecula Gorge, in the hills east of Sun City, and the hills north of Aguanga west of State Route 371. These may be still active or still suitable, however breeding activity has not been confirmed or mentioned in recent communications. Additional records are also reported for Elsinore peak, Rawson Canyon, and possibly Double Butte (P. Bloom 2001 pers. comm.) and Mesa de Burro on the Santa Rosa Plateau, on a transmission line in San Timoteo Canyon and possibly in the Box Springs Mountains and on Arlington Mountain (LaPré 2002; Tierra Madre Consultants Inc. 1999). The nest on the transmission line in San Timoteo Canyon appears to likely be a golden eagle based on size of the chicks and nest, however the identification was not confirmed (Tierra Madre Consultants Inc. 1999). The nest sites in the Box Springs Mountains and on Arlington Mountain appear to be abandoned (LaPré 2002).
Golden eagles have been recorded in larger numbers or repeated numbers indicating higher usage in the Badlands, at Lake Perris and environs, at Lake Mathews-Estelle Mountain, Alberhill/ Meadowbrook, Wildomar, Temecula, French Valley, Lake Skinner, Double Butte (Patten 1998 pers. comm.) and in the Prado Basin (Hays 1999 pers. obs.). Additional localities include Beaumont area and Santa Rosa Plateau in very low numbers.
Biology
Genetics: No information is available in the literature or was reviewed.
Diet and Foraging: The golden eagle eats mostly lagomorphs and rodents; it also takes other medium to large mammals, birds, reptiles, and some carrion (Johnsgard 1990; Olendorff 1976). The golden eagle is considered to be an opportunistic forager (Olendorff 1976). In southern California, the prey of golden eagles is made up predominantly of the California ground squirrel (Spermophilus beecheyi) and the Audubon cottontail (Sylvilagus audubonii) (Hoechlin 1976).
The golden eagle needs a broad expanse of open country for hunting including grasslands, deserts, savannahs, and early successional stages of forest and shrub habitats (Johnsgard 1990). It soars 30-90 meters (98-297 feet) above the ground in search of prey, or makes low, quartering flights, often 7-8 meters (23-26 feet) above ground. Occasionally it searches from a perch and flies directly to the prey (Carnie 1954). Sometimes it pirates food from other predators. Hunting in pairs is apparently common with one member of the pair chasing the prey to exhaustion and the other swooping down to kill the prey (Terres 1980). Foraging takes place over large areas of grassland and open chaparral or coastal sage scrub as well. In parts of Idaho, golden eagles have been shown to select areas with abundant and large shrub patches which provide preferential jackrabbit habitat (Marzluff 1997).
Daily Activity: The golden eagle exhibits year-long, diurnal activity (Zeiner et al. 1990). The golden eagle spends most of the day perched (78 to 85 percent of the day) and the rest of the day in flight (Collopy and Edwards 1989).
Reproduction: Nesting of the golden eagle is primarily restricted to rugged, mountainous country, with canyon and escarpments (Garrett and Dunn 1981; Johnsgard 1990; Call 1978). Most of the nests are located on cliffs with some nests occurring in Douglas-fir, pine trees, or other large trees (McGahan 1968). Nest locations tend to be more closely associated with topographic heterogeneity than with a particular vegetation type (Call 1978). There is a high frequency of nest locations on granite cliffs. Approximately 85 percent of all nest areas overlook or are on the opposite side of the ridge from large valleys or areas of relatively low topographic heterogeneity and open vegetation (Scott 1985). Pairs may build more than one nest and attend them prior to laying eggs (McGahan 1968). Each pair can have up to 10 nests, but only 2-3 are used in rotation. Some pairs use the same nest each year, while others use alternate nests year after year, and still others apparently may nest only every other year. The same nest may even be used by succeeding generations of eagles (Terres 1980).
The golden eagle builds a large platform nest, often 3 meters (10 feet) across and 1 meter (3 feet) high, of sticks, twigs, and greenery. It breeds from late January through August, with a peak in March through July. The clutch size is 1-3 eggs, usually 2 eggs (McGahan 1968). Eggs are laid in early February to mid-May. The young birds hatch several days apart, thus the older, stronger eaglets often kill their smaller siblings, and the parents do not interfere (Terres, 1980). Incubation lasts 43-45 days (Beebe 1974), and the nestling period usually is 65-70 days. Parental care continues into August and family groups remain together into November (Scott 1985).
Survival: The breeding success of undisturbed golden eagle pairs, as estimated by Brown and Amadon (1968), may vary from 1.4 to 0.5 young per pair per year with an average of 1.4 in Montana. Where persecuted by man, the breeding success is lower, down to 0.4 or less. The young bird does not breed for about four years and the average expectation of life of adults in the wild, assuming a 75 percent loss of young before maturity, is approximately ten years (Brown and Amadon 1968). In the wild, they likely live to at least 20 years (Brown and Amadon 1968).
Dispersal: After the young golden eagles have flown, they remain in the vicinity of the nest for about two weeks and thereafter follow the parents away from the site (Brown and Amadon 1968). In some populations, they are thought to be dependent on parental assistance for about three months after learning to fly, and normally separate from the parents about October. The young often appear near the nest site in the early part of the following breeding season and immature golden eagles sometimes frequent a nest site for several years before they finally breed there. The site then used by the offspring of the established pair may be old or new or one that has been unoccupied for many years (Brown and Amadon 1968).
Socio-Spatial Behavior: The home range of the golden eagle is probably the same as the territory (Zeiner et al. 1990). The size of the home range is related to prey density and availability, and the openness of terrain. Territory is estimated to average 57 sq. km (22 sq. mi) in Idaho (Beecham and Kochert 1975), 171-192 sq. km (66-74 sq. mi) in Montana (McGahan 1968), 23 sq. km (9 sq. mi) in Utah (Smith and Murphy 1973), 93 sq. km (36 sq. mi) in southern California (Dixon 1937), and 124 sq. km (48 sq. mi) in northern California (Smith and Murphy 1973). Although total home range can be very large, individuals tend to focus on a smaller core area within the total home range (Marzluff et al. 1997).
Community Relationships: The golden eagle occasionally preys on domestic calves and lambs. It may compete with ferruginous hawks for small mammals, and with California condors for carrion (Zeiner, et al. 1990). Golden eagles defend nest areas from conspecifics and appear to defend part of their home range, however there can be substantial overlap between the home ranges of adjacent pairs (Scott 1985).
Threats to Species
The golden eagle was formerly considered common within suitable habitats in California (Grinnell and Miller 1944), the species was more recently judged to be uncommon throughout much of California (Garrett and Dunn 1981). As is intimated above, the golden eagle avoids settled areas and therefore has almost certainly declined in the Plan Area and California as a whole within the past century due to loss of large unfragmented habitat areas (Grinnell and Miller 1944). Only four pairs of golden eagles have recently nested in adjacent Orange County and the Chino Hills in any given recent year, and these pairs are usually unsuccessful in raising young (Hamilton and Willick 1996). Additional threats to this species are human disturbance of nest areas leading to desertion of the nest in early incubation, urbanization, poaching, and electrocution from high tension wires (Remsen 1978; Thelander 1974). The issue of raptor electrocutions on power lines started receiving serious attention in the early 1970s. Several studies identified how raptors were being electrocuted, including golden eagles, and recommendations have been established to reduce the risk (Olendorff et al. 1981; Avian Power Line Interaction Committee 1996). Most bird electrocutions occur on distribution systems at the relatively lower voltages due to the closer spacing of the electrical conductors on the distribution systems. Single phase poles, three phase poles, and pole mounted transformers all pose an electrocution threat to raptors but can be retrofitted with various devices to reduce the risk (dcaccess.com 8/19/2002).
Special Biological Considerations
The golden eagle is sensitive to human disturbance and to land use changes that disrupt natural food supplies and nesting sites. Human activities are known to impact raptors by means such as : physically harming or killing eggs, young or adults; by altering habitat; and by disrupting normal behavior (Richardson and Miller 1997). Due to the broad range of direct and indirect human-associated impacts, establishment of buffer zones created around a nest location provide protection and work best if they include both a spatial and temporal restriction (Richardson and Miller 1997). A specific determination of the buffer distance required to prevent disturbance of nest sites has not been determined empirically for the golden eagle (Dave Bittner 1998 pers. comm.; Newton 1979). In one study, home ranges adjoining developed sections of a Plan Area were shown to be abandoned more often than interior areas, however, there is no distinct relationship between the proximity of nests to development and their probability or year of abandonment (Scott 1985). The loss of a nesting area could not be attributed to the loss of a specified amount of any vegetation type within 2.5 kilometers of nests (Scott 1985). In addition, the loss of suitable foraging habitat around active nests was equal to, or in some cases greater than, the loss around abandoned areas. In a study of golden eagles in San Diego County, the count of residences was the only variable measured that showed a significant correlation to the number of abandoned areas. The distance that this seems to come into play was 1.6 kilometers (Scott 1985). A significantly larger number of active areas had no dwelling units within a radius of 1.6 kilometers while a significantly larger number of abandoned areas contained 50 or more dwelling units within the same radius (Scott 1985). In agreement with this species specific study, the analysis of various biologist concluded that for the golden eagle, a spatial buffer of 200 meters to 1.6 kilometers was recommended (Richardson and Miller 1997). Temporal buffers provide additional support to the spatial buffer and have been recommended to encompass all nesting activities and extend at least from the arrival of the adult birds in the nesting areas through the first few weeks of nestling development (Richardson and Miller 1997).
Less specific studies on establishment of buffers for species including the golden eagle have provided additional recommendations to the species specific study discussed above. A survey of biologists resulted in recommendations that activities such as geological, biological or soil surveys be kept to at least 500 meters from active nest sites (Suter and Joness 1981). Suter and Joness (1981) recommend that extended activities be kept at least 1 kilometer from nest sites to avoid nest abandonment and temporal buffers be used to supplement or may be used in place of spatial buffers.
Kochert, et al. (1999) studied the effects of fire on golden eagle reproductive success in Idaho and found that in burned territories, golden eagles were significantly less successful in raising young.
A principal components analysis reveals that the golden eagle selects the most inaccessible cliffs (higher and further away from tracks, roads, and villages). The search for inaccessibility for the eagle depends on the amount of human disturbance in the area. Site orientation only contributes to the nest site selection when there is adverse weather (Fernandez 1993).
The number of golden eagle pairs occupying nesting territories each year showed a significant decline through time in the Snake River Birds of Prey Area. An analysis of the factors contributing to this concluded that both jackrabbit abundance and winter severity were important in predicting the percentage of eagle pairs that laid eggs. This study demonstrated that prey and weather can interact to limit a large raptor's population productivity (Steenhof et al. 1997).
As identified above under Threats, electrocution still poses potential problems for raptors, including the golden eagle, even though significant advances have been made in the design of power poles to avoid electrocution (Avian Power Line Interaction Committee 1996). The most important aspect in the design of power poles is the spacing of the conductors, which should be greater than 6 feet (Olendorff et al. 1981). Although it may not be economically feasible to protect all power poles, a study in Idaho estimated that 95% of electrocutions would be prevented by upgrading 2% of the poles (Nelson and Nelson 1976). Determining which poles pose a threat and retrofitting those poles with a suitable protection device has been recommended in other regions. Generally, the electrocution problem occurs on lower voltage poles because the large transmission towers with the higher voltage have a greater spacing of conductors. The recommendations for the potential problem power poles include: insulate the conductor for single phase poles; install perch guard, raised perch, or insulate the conductor on three phase poles; insulate jumper wires, cover bushings and lightning arresters with insulating caps and coat transformers with non-conductive paint for pole mounted transformers; and increase the distance between phase conductors and insulate conductors on compact armless poles (dcaccess.com 8/19/2002).
LITERATURE CITED
AOU (American Ornithologists' Union). 1998. Check-List of North American Birds. Seventh Edition. American Ornithologists' Union, Washington, D.C. 829 pp.
Avian Power Line Interaction Committee. 1996. Suggested Practices for Raptor Protection on Power Lines: The State of the Art in 1996. Edison Electric Institute, Raptor Research Foundation, Washington, D. C.
Beebe, F. L. 1974. Field studies of the Falconiformes of British Columbia. Brit. Col. Prov. Mus. Occas. Pap. No. 17. 163pp.
Beecham, J. J., and M.. N. Kochert. 1975. Breeding biology of the golden eagle in southwestern Idaho. Wilson Bull. 87:506-513.
Bittner, Dave . 1998. Wildlife Research Institute. pers. comm. on November 13.
Bloom, P. 2001. pers. comm.
Brown, L., and D. Amadon. 1968. Eagles, hawks and falcons of the world. 2 Vols. Country Life Books, London. 945pp.
Call, M. W. 1978. Nesting habitats and surveying techniques for common western raptors. Technical Note TN-316. U.S. Department of the Interior - Bureau of Land Management, Denver Service Center.
Carnie, S. K. 1954. Food habits of nesting golden eagles in the coast ranges of California. Condor 56:3-12.
Cleary-Rose, K. 2002. USFWS. Pers. comm.
Collopy, M. W., and T. C. Edwards, Jr. 1989. Territory size, activity budget, and role of undulating flight in nesting golden eagles. J. Field Ornithology 60: 43-51.
Dcaccess.com. 8/19/2002. Electrocution of Raptors on Power Lines. Http://www.dcaccess.com/ ~gnealon/electric.htm.
Dixon, J. B. 1937. The golden eagle in San Diego County, California. Condor 39: 49-56.
Garrett, K. and J. Dunn. 1981. Birds of Southern California: Status and Distribution. Los Angeles Audubon Society. 407 pp.
Grinnell, J. and A.H. Miller. 1944. The Distribution of the Birds of California. Pacific Coast Avifauna Number 27. Copper Ornithological Club, Berkeley, California. Reprinted by Artemisia Press, Lee Vining, California; April, 1986. 617 pp.
Fernandez, C. 1993. Selection de falaises pour la nidification chez l'aigle royal Aquila chrysaetos. Alauda 61: 105-110.
Hamilton, R. and D.R. Willick. 1996. The Birds of Orange County, California: Status and Distribution. Sea and Sage Press, Irvine, California. 150 pp. with appendices.
Hays, L.. R.. 1999. USFWS, pers. obs.
Hoechlin, D. R. 1976. Development of golden eaglets in southern California. Western Birds 7: 137-152.
Johnsgard, P.A. 1990. Hawks, eagles, and falcons of North America. Smithsonian Institution Press, Washington, D.C.
Kochert, M. N., K. Steenhof, L.B. Carpenter and J. M. Marzluff.. 1999. Effects of fire on golden eagle territory occupancy and reproductive success. Journal of Wildlife Management 63: 773-780.
LaPré, L. 2002. Audubon Society Comments on the Western Riverside County MSHCP. Memo from the San Bernardino Valley Audubon Society. 4 pp.
Marzluff, J. M., S. T. Knick, M. S. Vekasy, L. S. Shcueck, and T. J. Zarriello. 1997. Spatial use and habitat selection of golden eagles in southwestern Idaho. Auk 114: 673-687.
McGahan, Jerry. 1968. Ecology of the Golden Eagle. The Auk 85: 1-12.
Nelson, M. W. and P. Nelson. 1976. Powerlines and birds of prey. Idaho Wildlife Review 28: 3-7.
Newton, I. 1979. Population ecology of raptors. Buteo Books, Vermillion, South Dakota. 399 pp.
Olendorff, R. R. 1976. The food habits of North American golden eagles. Amer. Midl. Nat. 95:231-3-236.
Oldendorff, R. R., A. D. Miller, and R. N. Lehman. 1981. Suggested Practices for Raptor Protection on Power Lines: The State of the Art in 1981. Raptor Research Foundation., St. Paul, Min. 111 pp.
Palmer, R. S. 1988. Handbook of North American Birds, Volume 5, Yale University Press, New Haven, Connecticut.
Patten, Michael. 1998. Riverside County Editor for American Field Notes and Past Secretary, California Bird Records Committee, pers. comm.
Remsen, J. V., Jr. 1978. Bird species of special concern in California. Calif. Dep. Fish and Game, Sacramento. Wildl. Manage. Admin. Rep. No. 78-1. 54 pp.
Richardson, C. T. and C. K. Miller. 1981. Recommendations for protecting raptors from human disturbance: A review. Wildlife Society Bulletin 25: 634-638.
Scott, T. A. 1985. Human impacts on the golden eagle population of San Diego County from 1928 to 1981. Ph.D. Thesis, San Diego State University 98 pp.
Smith, D. G., and J. R. Murphy. 1973. Breeding ecology of raptors in the eastern Great Basin of Utah. Brigham Young Univ., Provo. Sci. Bull. Biol. Ser. 18, No. 3. 76pp.
Steenhof, K., M. N. Kochert, and T. L. McDonald. 1997. Interactive effects of prey and weather on golden eagle reproduction. J. Animal Ecology 66: 350-362.
Terres, J. K. 1980. The Audubon Society Encyclopedia of North American Birds. Alfred A. Knopf, New York, New York. 1109pp.
Thelander, C. G. 1974. Nesting territory utilization by golden eagles (Aquila chrysaetos) in California during 1974. Calif. Dept. Fish and Game, Sacramento. Wildl. Manage. Branch Admin. Rep. 74-7. 19pp.
Tierra Madre Consultants, Inc. 1999. Winter Raptor Surveys in the Badlands of Western Riverside County. Prepared for Riverside County Parks Department. 9 pp.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
grasshopper sparrow (Ammodramus savannarum)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
grasshopper sparrow (Ammodramus savannarum)
Status:
State: None
Federal: Partners in Flight Priority Bird Species; Species of Management Concern
GROUP DESIGNATION AND RATIONALE
Group 2
The grasshopper sparrow is widely, but sparsely, distributed throughout the MSHCP Plan Area within suitable habitat in the Riverside Lowlands, Santa Ana Mountains, and San Jacinto Foothills Bioregions. It is absent from the higher elevation Bioregions and the desert transition Bioregions. The grasshopper sparrow has well known and restricted habitat requirements. It is sensitive to edge effects and requires relatively large blocks of contiguous habitat.
Grasshopper sparrow habitat requirements are well known. Once conservation has been achieved, and specific locations that support Core Areas are known, it is anticipated that this species will respond well to a landscape level of management with site-specific requirements. It has therefore been included in Group 2.
The MSHCP Conservation Area configuration is expected to provide long-term conservation of the species. However, the grasshopper sparrow is a grassland species and as much as 70% of the mapped grassland within the Plan Area would be outside the MSHCP Conservation Area. Because the grasshopper sparrow does not tolerate fragmentation and most of the grassland in the Plan Area will be lost, Incidental Take of this species is not included in this permit until conservation of the species in the Plan Area has been demonstrated by reaching Objective 2 below.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 38,690 acres of suitable habitat for the grasshopper sparrow including grassland habitat within the Riverside Lowland, San Jacinto Foothills, and Santa Ana Mountains Bioregions.
Objective 2
Within the MSHCP Conservation Area, maintain occupancy within 3 large Core Areas (100 percent) and at least 3 of the 4 smaller Core Areas (75 percent) in at least 1 year out of any 5 consecutive year period. In order for this species to become a Covered Species Adequately Conserved, the following conservation must be demonstrated: Include within the MSHCP Conservation Area at least 8,000 acres in 7 Core Areas. Core areas may include the following: 1) Prado Basin, 2) Lake Skinner/Diamond Valley Lake/Johnson Ranch area, 3) Lake Mathews-Estelle Mountain, 4) Badlands, 5) Box Springs, 6) Santa Rosa Plateau/Tenaja, 7) Kabian Park, 8) Steele Peak, 9) Sycamore Canyon, 10) Potrero, and 11) Mystic Lake/San Jacinto Wildlife Area. Three of the 7 Core Areas will be large, consisting of a minimum of 2,000 acres of grassland habitat or grassland-dominated habitat (<20 percent shrub cover). The other 4 Core Areas may be smaller but will consist of at least 500 acres of contiguous grassland habitat or grassland-dominated habitat (<20 percent shrub cover). Five of the 7 Core Areas will be demonstrated to support at least 20 grasshopper sparrow pairs with evidence of successful reproduction within the first 5 years after permit issuance. Successful reproduction is defined as a nest which fledged at least one known young.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
The grasshopper sparrow uses predominantly open grassland with use of some other habitats including alluvial, playa, and sparse coastal sage scrub when sufficient amounts of intermittent grass or grassland habitat are available (Garrett and Dunn 1981). The grasshopper sparrow breeds and may winter, in the MSHCP Plan Area. Grasslands are the most important habitat for the species and are the focus of this conservation analysis. The Plan Area supports, in total, approximately 132,040 acres of grassland. Table 1 shows the conservation and loss of habitat for the grasshopper sparrow. Approximately 38,690 acres (29 percent) of the grassland will be conserved in the Criteria Area or existing Public/Quasi-Public lands. This includes conservation of 2,630 acres of valley and foothill (native) grasslands which are the preferred habitat of the grasshopper sparrow although non-native grasslands are used by the species as well.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
GRASSHOPPER SPARROW
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| Riverside Lowland, San Jacinto Foothills, and Santa Ana Mountains Bioregions | |||||||
| Non-native Grassland | 129,300 | 17,910 | 18,150 | 36,060 | 11,240 | 82,000 | 93,240 |
| Valley and Foothill Grassland | 2,740 | 310 (11%) |
2,320 (85%) |
2,630 (96%) |
90 (3%) |
20 (1%) |
110 (4%) |
| TOTAL | 132,040 | 18,220 (14%) |
20,470 (16%) |
38,690 (29%) |
11,330 (9%) |
82,020 (62%) |
93,350 (71%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
As described below under Data Characterization, 18 of the 48 recent point localities have a high location precision. Of these 18 point localities, 8 will be inside the Criteria Area or Public/Quasi-Public lands. Three locations are within the rural/ mountainous category. Seven point localities will be outside of the MSHCP Conservation Area, two of which are recorded for residential land use and may no longer be extant.
Conservation of large areas of grassland is important to the grasshopper sparrow because it is sensitive to edge effects and has large area requirements. At least 7 potential core population areas, 3 large (>2000 acres) and 4 smaller (>500 acres), consisting of contiguous grassland or grassland-dominated habitat, will be conserved. Core areas may include the following: (1) Prado Basin, (2) Lake Skinner/Diamond Valley Lake/Johnson Ranch area, (3) Lake Mathews-Estelle Mountain, (4) Badlands, (5) Box Springs, (6) Santa Rosa Plateau/Tenaja, (7) Kabian Park, (8) Steele Peak, (9) Sycamore Canyon, (10) Potrero, and (11) Mystic Lake/San Jacinto Wildlife Area. Three of the 7 Core Areas will be large, consisting of a minimum of 2,000 acres of grassland habitat or grassland-dominated habitat (<20 percent shrub cover). The other 4 Core Areas may be smaller but will consist of at least 500 acres of contiguous grassland habitat or grassland-dominated habitat (<20 percent shrub cover). Five of the 7 Core Areas will be demonstrated to support at least 20 grasshopper sparrow pairs with evidence of successful reproduction within the first 5 years after permit issuance. Successful reproduction is defined as a nest which fledged at least one known young. Additionally, the MSHCP Conservation Area will maintain occupancy within 3 large Core Areas (100 percent) and at least 3 of the 4 smaller Core Areas (75 percent) in at least 1 year out of any 5 consecutive year period.
An analysis of edge effects within the Plan Area, indicates that the blocks of habitat identified as conserved are composed largely of areas without urban or agricultural edges; that is, they are in the range of 601 to 120,000 feet from urban or agriculture lands with the proposed MSHCP Conservation Area design. Those core population areas of the grasshopper sparrow that receive some conservation but show strong or moderate edge effects are not considered conserved. Once under management, conservation of this species will be considered from a landscape perspective because the species' nesting and foraging requirements are well known. Additionally, there will be definable core population areas for focused conservation efforts.
MSHCP Conservation Area Configuration Issues
Several large blocks of habitat supporting the current known and potential locations of the grasshopper sparrow will be conserved as Criteria Area, and Public/Quasi-Public designations, including the Prado Basin, Lake Mathews-Estelle Mountain, Lake Skinner/Diamond Valley Lake, and Wasson Canyon. As identified above, the species occurs within the MSHCP Plan Area as a breeding and potentially as a wintering resident and as such, the proposed MSHCP Conservation Area is expected to provide adequate habitat for nesting and foraging. Core Areas are linked to provide dispersal habitat for grasshopper sparrows, although linkage areas are not necessarily composed of grassland habitats. The Prado Basin area is linked along the Santa Ana River to areas outside the Plan Area. The Lake Mathews-Estelle Mountain is linked to the Wasson Canyon area within the Alberhill and Temescal Wash areas. The Lake Skinner/Diamond Valley Lake area is linked to the Wasson Canyon area by the Sedco Hills and Hogbacks through the AD 161 Mitigation area and two Proposed Constrained Linkages.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 38,690 acres of suitable Conserved Habitat. In addition, implementation of Objective 2 for this species will provide conservation of at least 7 Core Areas, 3 large (>2,000 acres) and 4 smaller (>500 acres), consisting of contiguous grassland or grassland-dominated habitat and maintenance of occupancy and successful breeding within these Core Areas. However, the Plan does not require surveys or habitat assessments for this species to inform assemblage of the MSHCP Conservation Area. It is possible that the overall acreage goal of 153,000 new acres of conservation could be achieved without conserving the 7 Core Areas of grassland habitat, leaving the species vulnerable to extirpation in the Plan Area and failing to meet the objectives of the Plan. Under those circumstances the Incidental Take of the species will not be covered if the species were to be listed during the life of the Plan.
INCIDENTAL TAKE
The Incidental Take of the grasshopper sparrow is difficult to quantify due to our limited knowledge of its distribution and abundance within the Plan Area. The maximum level of Incidental Take of grasshopper sparrow can be anticipated by the loss of the number of acres of habitat that will become unsuitable for this species. About 93,350 acres (71 percent) of habitat for the grasshopper sparrow will be outside the MSHCP Conservation Area and individuals within this habitat will be subject to Incidental Take consistent with the Plan. A total of 110 acres, 4 percent, of the native grasslands will be outside of the MSHCP Conservation Area. Three locations within the location database are within the Rural/Mountainous category. Seven point localities will be outside of the MSHCP Conservation Area, two of which are recorded for residential land use and may no longer be extant.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The UCR location database contains approximately 56 location records for the grasshopper sparrow dated from 1889 to 1999. Approximately 48 of these records are relatively recent (within the past 10 years) and 18 of these are precise locations. Most of these locations coincide with non-native grassland or sage scrub and would likely be extant. Approximately two of these records are located within residential habitat and may no longer exist. It is likely that the grasshopper sparrow is more numerous within the Plan Area within suitable habitat, but has not been reported due to the lack of focused surveys, the difficulty of detection and possibly lack of recording the locations of the species.
There is a moderate amount of literature available for this species. There are some thorough natural history accounts and some general distributional studies available.
Habitat and Habitat Associations
The grasshopper sparrow generally prefers moderately open grasslands and prairies with patchy bare ground. However, they select different components of vegetation depending on the grassland ecosystem. They occupy lusher areas with shrub cover in the arid grassland of the southwest and west but select sparser vegetation in the east and mid-west such as tall grass and short grass prairie, native palmetto, wire grass prairie, dry or well-drained native and cultivated grassland in the east and fire-induced grassland in the northern mid-west (Vickery 1996). The grasshopper sparrow typically avoids grassland with extensive shrub cover, although some level of shrub cover is important for birds in the western regions. In Georgia, it is absent in fields with greater than 35 percent shrub cover; it tolerates moderately brushy habitat in Massachusetts, and in southeastern Arizona, it prefers grasslands with shrubs (Vickery 1996).
During the winter, grasshopper sparrows may migrate from the breeding grounds and occupy weedy fields with scattered trees (Dunning 1989). They appear to use abandoned croplands that are dominated by grassy plant species. The habitat area used for wintering may be an early successional stage. Grasshopper sparrows may winter in these areas in mixed flocks with other sparrow species, however, it does not occur in conspecific flocks for wintering (Dunning 1989).
Grasshopper sparrows in California breed (and primarily apparently winter) on slopes and mesas containing grasslands of varying compositions (Grinnell and Miller 1944; Garrett and Dunn 1981). The species frequents dense, dry or well-drained grassland, especially native grassland with a mix of grasses and forbs for foraging and nesting. Apparently, thick cover of grasses and forbs is essential for concealment. They require fairly continuous native grassland areas with occasional taller stems for breeding areas (Garrett and Dunn 1981). They especially occur in grasslands composed of a variety of grasses and tall forbs with scattered shrubs for singing perches (Zeiner et al. 1990). Grasshopper sparrows use a variety of forb species for perches and choose them predominantly on the basis of their height rather than the specific plant species (Payne, et al. 1998). Although shrub and forb species are used for perching, they tend to avoid grassland areas with extensive shrub cover and the presence of native grasses is less important than the absence of trees (Smith 1963; Vickery 1996).
Biogeography
The grasshopper sparrow breeds from eastern Washington eastward to southern Maine southward to southern California, northernmost Mexico and Virginia. The species has a disjunct distribution through the more western portion of the United States and is not present within the mountainous and desert regions. It occurs in the areas east of the Rocky Mountains from Canada to the southern states as a breeding resident, wintering south into Florida and Mexico. It is a year round resident in the western states and in the southern portions of the southeastern states (Vickery 1996).
Grasshopper sparrows winter from California to North Carolina south through Middle America to Costa Rica (AOU 1998). In southern California, the species occurs locally in appropriate habitats west of the deserts and has nested to 1,500 meters in the San Jacinto Mountains (Garrett and Dunn 1981). It appears to be very rare to absent from the region in the winter but may be overlooked (Garrett and Dunn 1981).
Zeiner summarized the distribution, abundance, and seasonality of the grasshopper sparrow for California as follows. It is an uncommon and local, summer resident and breeder in foothills and lowlands west of the Cascade-Sierra Nevada crest from Mendocino and Trinity counties south to San Diego County. The species also has been found in Pete's Valley, Lassen County, and Shasta Valley, Siskiyou County. It is secretive in the winter and may occur more regularly than indicated by infrequent records, chiefly in coastal southern California (Grinnell and Miller 1944, McCaskie, et al. 1979, Garrett and Dunn 1981).
Populations of the grasshopper sparrow, especially the eastern most and western most subspecies, have declined by 69 percent across the United States since the late 1960s. In Illinois, the loss of prairie habitat is responsible for earlier population declines (Vickery 1996). It was formerly more widespread through the Riverside area to Beaumont (Garrett and Dunn 1981).
Known Populations Within Western Riverside County
The species apparently occurs locally throughout much of western Riverside County in suitable habitat in the Riverside Lowlands, San Jacinto Foothills and Santa Ana Mountains Bioregions (Garrett and Dunn 1981). The database records are relatively sparse but indicate the species occurs within the central portion of the Plan Area and is predominantly located in the south-central area although it was recently recorded for the Lake Perris area, Prado Basin, and south to the Temecula Valley east to Lake Skinner (Cooper 2001). They are absent at higher elevations. Populations appear to fluctuate widely in spite of available suitable habitat possibly due to low reproductive success rate and low return rates of breeding birds to their nesting areas (Smith 1963).
Grasshopper sparrows apparently are most heavily concentrated in the Prado Basin (although not recorded in the U.C. Riverside database), Santa Rosa Plateau, and Lake Skinner, within observations at Kabian Park areas and, possibly, in the Lake Mathews area (Hays 1999 pers. obs.; Patten 1998 pers. comm.). Studies by the Audubon Society indicate the grasshopper has been observed within the Lake Perris/Mystic Lake/San Jacinto Wildlife Area, (Cooper 2001). Based on the information provided by the USFWS and the database for the species the Core Areas appear to include the Prado Basin, Santa Rosa Plateau, Lake Skinner/Diamond Valley Lake area, Lake Mathews-Estelle Mountain, Wasson Canyon, and Murrieta Hot Springs area.
Biology
Genetics: Protein and mtDNA comparisons of the grasshopper sparrow reveal greater genetic differentiation in the genus Ammodramus than among most avian congeners, suggesting a possible polyphenetic structure (Vickery 1996).
Diet and Foraging: The grasshopper sparrow feeds primarily on insects, especially Orthoptera; it also eats other invertebrates and grass and forb seeds. There is a large proportion of grasshoppers in the diet, with most capture attempts aimed at the grasshopper thorax (Vickery 1996). Seeds make up a larger portion of the diet during the winter (Vickery 1996). The grasshopper sparrow searches for insect prey on the ground and in low foliage within relatively dense grasslands, sometimes scraping in the litter. The grasshopper sparrow is a visual predator, foraging exclusively on the ground and exposed bare ground is critical for effective foraging.
Daily Activity: The grasshopper sparrow exhibits year-long, diurnal activity (Zeiner, et al. 1990). The grasshopper sparrow migrates at night (Vickery 1996).
Reproduction: The grasshopper sparrow builds its nest of grasses and forbs in a slight depression in the ground or hidden at the base of an overhanging clump of grasses or forbs (Bent 1968, Zeiner, et al. 1990). The grasshopper sparrow builds a distinctive ground nest that is very difficult to locate, usually domed with overhanging grasses with a side entrance, somewhat similar to an ovenbird nest (Vickery 1996).
The grasshopper sparrow breeds from early April to mid-July, with a peak in May and June. The clutch size usually is 4 or 5 eggs, sometimes 3 or 6, with the second clutch generally being smaller (Vickery 1996). It may raise 2 or 3 broods per year. Incubation is approximately 11-12 days, by the female alone. The altricial young are tended by the female predominantly; the male reacts to predators near the nest but also provides food for the young. Adult and juvenile nonparental attendants also are known to feed the young. The nonparental attendants may make 9 to 50 percent of the provisioning visits to the nests (Vickery 1996). The young leave the nest at about nine days, although they are still unable to fly (Harrison 1978).
Survival: A study of a grasshopper sparrow population in Florida showed an annual survival rate of 0.60, with a mean longevity of 2.9 years and a maximum record of 6.6 years (Vickery 1996; Dean, et al. 1998).
Dispersal: Data on dispersal of the grasshopper sparrow is scarce because they are very secretive in winter. The grasshopper sparrow apparently winters rarely but regularly in California, chiefly along the southern coast. Summer residents arrive in March to May, and most migrate south in August or September. Fall migrants have been recorded in late September and early October on the Farallon Islands (DeSante and Ainley 1980). The young of the first brood have usually dispersed from the natal territories when the adults are feeding the nestlings of the second brood (Vickery 1996).
Socio-Spatial Behavior: The territory size has not been studied in California but appears variable in size elsewhere, ranging from 0.3 to 1.7 hectares (0.8 to 4.3 acres) per pair (Wiens 1969, Kendeigh 1941, Smith 1963). In Wisconsin, Wiens (1969) reported 73 territories averaging 0.8 hectares (2.1 acres) and varying from 0.3 to 1.7 hectares (0.8 to 4.3 acres). Kendeigh (1941) reported six territories averaging 1.4 hectares (3.4 acres) in lowa. In Pennsylvania, Smith (1963) reported 22 territories averaging 0.8 hectares (2.03 acres) and varying from 0.5-1.3 hectares (1.2 to 3.3 acres).
Community Relationships: The grasshopper sparrow may form semicolonial breeding groups of 3-12 pairs, but apparently does not form conspecific flocks in winter. The abundance fluctuates markedly locally and from year to year possibly due to low reproductive success rate and low return rates of breeding birds to their nesting areas (Ehrlich, et al. 1988).
Threats to Species
Continuing threats to the species apparently include habitat loss, degradation, and fragmentation. Extensive and intensive grazing in western North America has had a negative impact on this species (Vickery 1996). Garrett and Dunn (1981) concluded that the grasshopper sparrow has declined as breeder in recent decades because of development of open hilly areas which include its preferred habitat. Brown-headed cowbird parasitism does occur but is generally considered low (Vickery 1996).
Predation appears to be the major cause of nest failure in one population of the grasshopper sparrow (Perkins et al. 1998). Predation rates appear to be highest for nests placed in smaller grassland areas (less than 15 ha.) and for areas adjacent to edges composed of wooded areas (Burger et al. 1994).
Special Biological Considerations
The species is most easily detected in the Plan Area (and California as a whole) in the breeding season; migrants and wintering birds are secretive and are rarely observed (Garrett and Dunn 1981).
Three primary management techniques have been used and are recommended for this species: prescribed burning, grazing, and mowing. Each type of management has different impacts depending on the type of grassland ecosystem. Management of grasslands, including deferred mowing until after the breeding season, has successfully enhanced grasshopper sparrow populations (Vickery 1996). Areas that have scheduled mowing of grasslands, such as airports, are considered population sinks if the mowing is not scheduled to avoid the breeding season. The overall breeding success in areas where the timing of mowing is not scheduled to avoid the breeding season show a low nesting success of 14 percent which is too low to serve as a source population area (Kershner and Bollinger 1996).
In southern California, individuals have been shown to prefer high perennial grass cover and generally prefer sites more than one year after a burn (Vickery 1996). Relative abundance of wintering birds was greater in burned treatments. One study showed that a severe wildfire, which eliminated sagebrush cover, depressed the grasshopper sparrow densities for more than 3 years on a Montana shrubsteppe (Vickery 1996). It is recommended that unburned areas adjacent to burns be maintained to provide habitat for bird species that declined for a period after winter prescribed burning, which included the grasshopper sparrow (Reynolds and Krausman 1998).
In lush grassland habitat such as tallgrass prairie and eastern hayfields, light to moderate grazing is generally beneficial to the grasshopper sparrow, whereas grazing on arid grasslands on shortgrass prairie and in southeastern Arizona and California is detrimental (Vickery 1996).
A program entitled the "Conservation Reserve Program" (CRP) located in Missouri and six other mid-western states, has been attributed with substantially contributing to the conservation of grassland bird species (Johnson and Schwartz 1993). Reproductive rates and estimated fecundity for grasshopper sparrows were determined and documented that the CRP areas were source habitats, that is, fecundity exceeded levels necessary for grasshopper sparrows to maintain stable populations (McCoy, et al. 1999). The CRP areas were documented to contain the same species richness as non-CRP areas, however, the abundance of the grassland species within the CRP areas was 1.4 to 10.5 times greater in the CRP areas. Nest success in the CRP fields was 40 percent overall with predation documented to be the greatest cause of nest failure. Long-term farm set-aside programs such as the CRP, which establish perennial grass cover, seem to provide many benefits for grassland birds (Best, et al. 1997). However, it has been documented that although the CRP areas benefit grassland bird species, the conversion of these grassland areas to moderately grazed pasture lands will not affect the grassland birds species significantly (Klute, et al. 1997).
Minimum tract area of grassland required for grasshopper sparrows was determined to be 12 hectares (Vickery 1996). In another study in Illinois, grasshopper sparrows were only found within grassland area at least 16 hectares in size (Kobal, et al. 1999). It was determined that the area of grassland tract influences the perception of habitat suitability by this area-sensitive species more than the size or configuration of the management unit which may contain a variety of habitat types (Walk and Warner 1999). Predation rates are influenced by the degree of fragmentation and edge effects. In another study, predation was higher for areas less than 15 hectares and for nests located less than 60 meters from the edge of the habitat (Heckert 1994). In a different study, breeding success was not found to differ with closeness to the edge in limited habitat blocks, although nesting was avoided within 50 meters of edge habitats (Delisle and Savidge 1996).
Statistical analyses of grassland communities indicate that grasshopper sparrow presence or absence is influenced by the area or size of the grassland habitat fragment (Heckert 1994). In this study, which took place in Illinois, the estimated individual area requirement (area at which a species probability of occurrence equals 50 percent) for grasshopper sparrow is 30 hectares. The territory size for this species for some locations has been estimated at approximately 1 hectare, yet it will rarely occur in habitat blocks that are less than 10 times this size. The overall loss of breeding grassland habitat may be contributing to population declines. Studies have shown that rates of nest predation and nest parasitism are higher in the types of edges that dominate small grassland fragments and this increase in nest predation and parasitism may be sufficient to produce local and possibly regional declines in some grassland bird species (Heckert 1994).
LITERATURE CITED
AOU (American Ornithologists' Union). 1998. Check-List of North American Birds. Seventh Edition. American Ornithologists' Union, Washington, D.C. 829 pp.
Bent, A.C. 1968. Life histories of North American cardinals, grosbeaks, buntings, towhees, finches, sparrows, and allies. 3 Parts. Edited by O.L. Austin Fr. U.S. Natl.Mus.bull. 237. 1,889 pp.
Best, L. B., H. Campa, K. E. Kemp, R. J. Robel, M. R. Ryan, J. A. Savidge, H P. Weeks, and S. R. Winterstein. 1997. Bird abundance and nesting in CRP fields and crop land in the Midwest: a regional approach. Wildl. Soc. Bull. 25: 864-877.
Burger, L. D., L. W. Burger, and J. Faaborg. 1994. Effects of prairie fragmentation on predation on artificial nests. J. Wildl. Manage. 58: 249-254.
Cooper, D. S. 2001. California Important Breeding Areas. Audubon California. Los Angeles.
Dean, T. F., Delany, E. W. Chapman, and P. D. Vickery. 1998. Longevity and site fidelity of Florida grasshopper sparrows. J. Field Ornithology 69: 51-54.
Delisle, J. M. and J. A. Savidge. 1996. Reproductive success of grasshopper sparrows in relation to edge. Prairie Naturalist 28: 107-114.
Desante, D. F., and D. G. Ainley. 1980. The avifauna of the South Farallon Islands, California. Studies in Avian Biol. No. 4. Cooper Ornithol. Soc., Lawrence, KA. 104pp.
Dunning, J. B. 1989. Winter habitats and behavior of grasshopper sparrows near Athens, Georgia. Oriole 54: 51-53.
Ehrlich, P.R., D.S. Dobkin, and D. Wheye. 1988. The Birder's handbook. Simon and Schuster, New York. 787 pp.
Garrett, K. and J. Dunn. 1981. Birds of Southern California: Status and Distribution. Los Angeles Audubon Society. 407 pp.
Grinnell, J. and A.H. Miller. 1944. The Distribution of the Birds of California. Pacific Coast Avifauna Number 27. Copper Ornithological Club, Berkeley, California. Reprinted by Artemisia Press, Lee Vining, California; April, 1986. 617 pp.
Harrison, C. 1978. A field guide to the nests, eggs and nestlings of North American birds. W. Collins Sons and Co., Cleveland, OH. 416pp.
Hays, Lorren R. 1999, USFWS, pers. obs.
Herkert, J. R. 1994. The effects of habitat fragmentation on Midwestern grassland bird communities. Ecological Applications 4: 461-471.
Johnson, D. H. And M. D. Schwartz. 1993. The Conservation Reserve Program and grassland birds. Conservation Biology 7: 934-937.
Kendeigh, S.C. 1941. Birds of a prairie community. Condor 43: 165-174.
Kershner, E. L. , and E. K. Bollinger. 1996. Reproductive success of grassland birds at east-central Illinois airports. Amer. Midl. Nat. 136: 358-366.
Klute, D. S., R. J. Robel, and K. E. Kemp. 1997. Will conversion of Conservation Reserve Program (CRP) lands to pasture be detrimental for grassland birds in Kansas: Amer. Midl. Nat. 137: 206-212.
Kobal, S. N., N. F. Payne, D. R. Ludwig. 1999. Habitat/area relationships, abundance, and composition of bird communities in three grassland types. Trans. Ill. State Acad. Sci. 92: 109-131.
McCaskie, G., P. De Benedictis, R. Erickson, and J. Morlan. 1979. Birds of northern California, an annotated field list. 2nd ed. Golden Gate Audubon Soc., Berkeley. 84pp.
McCoy, T. D., M. R. Ryan, E. W. Kurzejeski, L. Burger. 1999. Conservation Reserve Program: Source or sink habitat for grassland birds in Missouri? J. Wildl. Management 63: 530-538.
Patten, Michael. 1998. Riverside County Editor for American Field Notes and Past Secretary, California Bird Records Committee, pers. comm.
Payne, N. F. , S. N. Kobal, and D. R. Ludwig. 1998. Perch use by seven grassland bird species in northern Illinois. Trans. Ill. State Acad. Sci. 91: 77-83.
Perkins, D. W., P. D. Vickery, T. F. Dean, and M. D. Scheuerell. 1998. Florida grasshopper sparrow reproductive success based on nesting records. Flor. Field Nat. 26; 7-17.
Reynolds, M. C. And P. R. Krausman. 1998. Effects of winter burning on birds in mesquite grassland. Wildlife Society Bulletin 26: 867-876.
Smith, R.L. 1963. Some ecological notes on the grasshopper sparrow. Wilson Bull. 75: 159-165.
Vickery, Peter D. 1996. Grasshopper sparrow (Ammodramus savannarum). In The Birds of North America, No. 239 (A. Poole and F. Gill, eds.) The Academy of Natural Sciences, Philadelphia, PA and The American Ornithologists' Union, Washington D.C.
Walk, J. W. And R. E. Warner. 1999. Effects of habitat area on the occurrence of grassland birds in Illinois. Amer. Midl. Nat. 141: 339-344.
Wiens, J. A. 1969. An approach to the study of ecological relationships among grassland birds. Ornithol. Monogr. No. 8. 93pp.
Wiens, J. A. 1973. Interterritorial habitat variation in grasshopper and savannah sparrows. Ecology 54: 877-884.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
great blue heron (Ardea herodias)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
great blue heron (Ardea herodias)
Status:
State: None
Federal: None
GROUP DESIGNATION AND RATIONALE
Group 2
The great blue heron is expected to be relatively well-distributed throughout the MSHCP Plan Area within its suitable habitat. It likely occurs at almost all of the open water bodies where emergent or riparian vegetation is present and many of the playas and riparian drainages that may provide foraging opportunities as well as many irrigation ditches, ponds and areas where suitable foraging opportunities are present. There are no locations that have been recorded within the UCR database, thus the distribution of this species is based on anecdotal observation and expert opinion. Several areas are likely Core Areas for this species, including Mystic Lake/San Jacinto Wildlife Area, Santa Ana River/Prado Basin, Lake Skinner, and Collier Marsh. The breeding locations, which have been documented as active or historic, are located at specific sites that require conservation. Because it is well known for using emergent habitat, riparian areas for nesting, ponds and other aquatic habitat, but has specific locations that are used for breeding, it is assumed that this species will respond to a landscape level of management with site-specific requirements (e.g., breeding rookeries).
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 16,560 acres of suitable nesting and foraging habitat for the great blue heron including freshwater marsh, playas and vernal pools, riparian scrub, woodland, and forest, and cismontane alkali marsh.
Objective 2
Include within the MSHCP Conservation Area at least the 3 known breeding locations, in the Santa Ana River/Prado Basin (9,670 acres), Lake Skinner area (Existing Core J; 24,370 acres), and Collier Marsh areas (Proposed Linkage 2; 160 acres).
Objective 3
A 100-meter buffer will be established around the Core Areas identified in Objective 2 as they are incorporated into the MSHCP Conservation Area.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
The great blue heron is one of the most common and most widespread of the herons, is found in a variety of aquatic habitats, and may use more forested riparian areas for nesting (Garrett and Dunn 1981). Because they will use a relatively wide variety of wetlands for various parts of their life history, a wide range of habitats has been included for this analysis. For the purpose of the conservation analysis, potential habitat for the great blue heron has been separated into the primary breeding habitat which includes freshwater marsh and riparian scrub, forest, and woodland. The secondary habitat, which is composed only of foraging habitat includes playas and vernal pools and cismontane alkali marsh. Based on these habitats, the Plan Area supports approximately 20,560 acres of potential habitat for the great blue heron composed of 12,680 acres of primary breeding and foraging habitat and 7,880 acres of secondary foraging habitat. Table 1 shows the conservation of potential habitat for the great blue heron. Overall, approximately 9,840 acres (78 percent) of potential primary breeding and foraging habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public Lands. Approximately 6,720 acres (86 percent) of secondary foraging habitat will be conserved in Criteria Area or existing Public/Quasi-Public Lands.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
GREAT BLUE HERON
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| Riverside Lowlands and San Jacinto Foothills Bioregions | |||||||
| Primary Habitat for Breeding and Foraging | |||||||
| Freshwater Marsh | 470 | 170 | 240 | 410 | 0 | 60 | 60 |
| Riparian Scrub, Woodland, Forest | 12,210 | 3,570 | 5,860 | 9,430 | 180 | 2,600 | 2,780 |
| Subtotal Primary Habitat | 12,680 | 3,740 (30%) |
6,100 (48%) |
9,840 (78%) |
180 (1%) |
2,660 (21%) |
2,840 (22%) |
| Secondary Habitat for Foraging | |||||||
| Playas and Vernal Pools | 7,870 | 3,830 | 2,880 | 6,710 | 0 | 1,160 | 1,160 |
| Cismontane Alkali Marsh | 10 | 10 | 0 | 10 | 0 | 0 | 0 |
| Subtotal Secondary Habitat | 7,880 | 3,840 (49%) |
2,880 (37%) |
6,720 (86%) |
0 (0%) |
1,160 (14%) |
1,160 (14%) |
| TOTAL | 20,560 | 7,580 (37%) |
8,980 (44%) |
16,560 (81%) |
180 (1%) |
3,820 (18%) |
4,000 (19%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
In addition, the Riparian/Riverine Areas and Vernal Pools policy described in Section 6.1.2 of the MSHCP, Volume I, provides for conservation of wetlands, which provide habitat for this species, through avoidance and minimization. Mitigation for impacts to wetlands shall be incorporated in accordance with the "No Net Loss" policy of federal and state wetland regulations. The proposed mitigation shall be directly related to the functions and values of the wetland as related to this species and result in equivalent replacement.
As described below under Data Characterization, there are no records within the UCR database or CNDDB. No rookeries have been recorded for the Plan Area within the database or CNDDB. Information on anecdotal observations of rookeries was provided by the resource agencies (Hays 2002 pers. comm.; Moore 2002 pers. comm.). All three of these rookery locations are within the Criteria Area or Public/Quasi-Public Lands. Additionally, the rookery locations, if within a wetland area, will continue to receive protection by the wetland policy. Conservation of this species can be considered from a landscape perspective because the species has well identified habitat requirements.
In addition to the habitat conservation, there are definable locations composed of Core Areas for focusing conservation efforts which are included within the MSHCP Conservation Area. These conserved Core Areas include the 3 known breeding locations in the Prado Basin/Santa Ana River (9,670 acres), Lake Skinner (Existing Core J; 24,370 acres), and the rookery at Rome Hill adjacent to Collier Marsh areas (Proposed Linkage 2; 160 acres). A total of 34,200 acres of Core Areas as estimated by the subunit acreages and core and linkage acreages are conserved within the MSHCP Conservation Area. Additionally, as part of the reserve assembly, a 100-meter buffer will be established around the Core Areas identified above as they are incorporated into the MSHCP Conservation Area.
MSHCP Conservation Area Configuration Issues
Several large blocks of habitat including potential or historic foraging and nesting areas for the great blue heron will be conserved as Criteria Area and Public/Quasi-Public Lands including the Prado Basin, Santa Ana River, Lake Skinner, Diamond Valley Lake, Lake Mathews, Mystic Lake, San Jacinto Wildlife Area/Mystic Lake, Lake Perris, Wasson Canyon, Temecula and Murrieta creeks, San Timoteo Creek, Temescal Wash, Lake Elsinore area, and Vail Lake. The MSHCP Conservation Area will provide adequate habitat for foraging during nomadic visits to the area and migratory stopovers as well as habitat containing potential nest sites with adequate protection around each nest site and foraging areas during the breeding season. Foraging areas are provided at Vail Lake, Lake Skinner, Diamond Valley Lake, San Jacinto Wildlife Area/Mystic Lake, Lake Perris, Lake Elsinore, Lake Mathews, Prado Basin and Santa Ana River, and a variety of other smaller riparian and wetland areas. Potential and known nest sites are provided in the Collier Marsh area (Rome Hill), Lake Skinner, and Prado Basin and foraging for a potential breeding season is provided in the riparian and marsh areas within and around Collier Marsh, within the Santa Ana River system and within the large MSHCP Conservation Area around Lake Skinner. These MSHCP Conservation Area locations are interconnected as well, though the ability of this species to move long distances may reduce the importance of these linkages for this species.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 16,560 acres of suitable Conserved Habitat including 9,840 acres of primary breeding and foraging habitat and 6,720 acres of secondary foraging habitat. Additionally, the three core known or potential breeding locations, Prado Basin/Santa Ana River, Collier Marsh, and Lake Skinner area within large blocks of habitat are included in the MSHCP Conservation Area. As these Core Areas are incorporated into the MSHCP Conservation Area, a 100-meter buffer will be established around each Core Areas. The current population size of the great blue heron is unknown. Implementation of the MSHCP, including the conservation of existing or potentially occupied habitat, core populations, and current and historic nesting locations as described above, is anticipated to maintain the status of the species and its habitat within the MSHCP Conservation Area.
INCIDENTAL TAKE
The Incidental Take of the great blue heron is difficult to quantify at this time owing to our limited knowledge of the precise location and extent of nesting sites and the fact that losses may be masked by fluctuations in abundance and distribution during the life of the permit. However, the level of Take of great blue heron can be anticipated by the loss of the number of acres of habitat that will be impacted or become unsuitable for this species. About 2,840 acres (22 percent) of potential primary breeding and foraging habitat for the great blue heron will be outside the Criteria Area and Public/Quasi-Public Lands and individuals within these areas are subject to Incidental Take consistent with the Plan. Approximately 1,160 acres (14 percent) of potential secondary foraging habitat for the great blue heron will be outside the Criteria Area and Public/Quasi-Public Lands and individuals within these areas are subject to Incidental Take consistent with the Plan. No rookeries are anticipated to be subject to Incidental Take.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California Riverside GIS database, the California Natural Diversity Database (CNDDB), and available literature.
There are no data points in the UCR database and no records within the CNDDB for either foraging locations or rookeries for this species. Rookery records are being accumulated.
The available literature is low to moderate and provides baseline natural history information and habitat relationship analyses. Few controlled scientific studies have been conducted. Most of the information is provided within the general ornithological literature.
Habitat and Habitat Associations
The great blue heron breeds most commonly in isolated areas, such as wooded swamps or predator-free islands. Upland hardwood forest, forest-bordered lakes and ponds, and riparian woodlands are also used. Breeding sites are always near water (Butler 1992).
Great blue herons forage in a variety of habitat types, including marshes, shores, swamps, tidal flats, lakes, rivers, lagoons, riparian forests, and coastal wetlands. Any slow-moving, shallow water will suffice for foraging (Kaufman 1996). In a study of herons in British Columbia (Butler 1991), juveniles foraged in grasslands, adult females in estuarine marshes or the intertidal zone, and adult males along riverbanks. Foraging habitat for yearlings was not well documented in this study, but included estuaries and beaches. Insular herons prefer to forage in areas located away from the main channel and containing submergent or emergent vegetation (Thompson 1979, Hoffman 1978), while herons in coastal areas will forage in more exposed areas, such as mud flats and sandbars (Longley 1960, Edison Electric Institute 1980, Bayer 1978).
Biogeography
The great blue heron breeds from along the coast of southeast Alaska and British Columbia and the southern regions of the Canadian prairie provinces in the north, southward through the United States, Mexico, and Central America as far as Belize and Guatemala. The species also breeds on the Galapagos Islands and islands near Venezuela. Jamaica was historically a breeding site of the great blue heron (Butler 1992).
The winter range of this heron extends along the Pacific coast south of 610 N, throughout the United Sates, Mexico, Central America, the Caribbean, and the north and west coasts of South America as far south as Colombia. The bird is occasionally reported wintering in Hawaii (Butler 1992).
Known Populations Within Western Riverside County
No locations have been recorded in the CNDDB or the UCR database, although the great blue heron occurs in virtually all wetland habitats. Information on rookery locations, which would be considered the Core Areas for the species, was provided by the USFWS and CDFG (Hays 2002 pers. comm., Moore 2002 pers. comm.).
There are approximately 35 nesting pairs of great blue herons at Prado split amongst two locations: the southwesternmost portion of the Basin and Prado Regional Park. Focused surveys might turn up a few more pairs (Hays 2002 pers. comm.). Rookeries are also located at Lake Elsinore, on private property near Rome Hill within some trees and at Lake Skinner observed by K. Cleary-Rose, USFWS (Moore 2002 pers. comm.).
Biology
Genetics: The great blue heron is very similar morphologically (Bock 1956), behaviorally (Curry-Lindahl 1971), and genetically (Sheldon 1987) to two other herons: the South American Cocoi Heron (Ardea cocoi), and the Old World Grey Heron. However, since the ranges of the three taxa do not overlap, they are considered semi-species of one super-species (e.g., Hancock and Elliot 1978, Payne 1979).
The number of species within Ardea herodias has been debated in the past; however most of the North American A. herodias are agreed to belong to a single subspecies (herodias). The northwest subspecies is classified as A.h. fannini, and the Florida subspecies (great white heron) is classified as A.h. occidentalis (Butler 1992).
Morphology varies clinally, with southern birds trending towards larger body sizes than northern birds (Butler 1992).
Diet and Foraging: The great blue heron forages within almost any wetland habitat type. In addition, juveniles forage in upland fields and grasslands, especially in winter. Birds forage singly or with conspecifics (Butler 1992). The great blue heron may stand very still or walk very slowly in shallow water, waiting for prey to come near, then strike with a rapid thrust of the bill (Kaufman 1996). Birds may wade up to belly deep in water (Butler 1992) and have been observed to dive for food (Bent 1926, Dickinson 1947, Gordin 1977). Birds may also forage from floating objects (Kaufman 1996, Gordin 1977) and while floating (Jensen 1932).
The great blue heron's diet consists mainly of fish, but it will also consume salamanders, frogs, turtles, insects, snakes, birds, and rodents (Kaufman 1996). The heron has been seen stalking voles and gophers in fields. Voles comprise 24-40 percent of the diet of nestlings and are thought to be critical to juvenile winter survival in British Columbia (Butler 1991). Most prey are swallowed whole, and some are wetted before swallowing (Peifer 1979). The variable diet of the heron has been implicated as a causal factor for the species's ability to survive further north than other species of heron (Kaufman 1996).
Daily Activity: The great blue heron forages both at night and during the day (Kaufman 1996, Butler 1992). Peak feeding activity occurs near low tide for coastal herons. Behaviors such as pair formation, nest building, and courtship, occur just before or after feeding (Brandman 1976).
Reproduction: Most great blue herons reproduce in their second season (greater than 22 months of age) (Butler 1992).
In Chesapeake Bay, great blue heron nesting sites are living trees, but birds may also nest in dead trees or shrubs (USFWS 2001). Nest sites are variable, but are located high in trees, often from 20 to 60 feet high, but sometimes as high as 100 feet (Kaufman 1996). A variety of tree species may be used. Suitable nesting sites are "open" or have exposed limbs, allowing birds to enter and leave easily (Short and Cooper 1985). Occasionally nests are made in low shrubs (Behle 1958, Vermeer 1969) or on the ground on predator-free islands (Kaufman 1996, Taverner 1926, Gill and Mewaldt 1979). When trees are not available, great blue herons may also build nests in bulrushes, cacti (Rosenberg et al. 1991), sagebrush (Blus et al. 1980), duck blinds (Palmer 1962), channel markers (Henny and Kurtz 1978, Blus et al. 1980), or artificial nest platforms (Sandilands 1980).
The nest is a large platform of sticks, up to 1.25 meters wide and 0.5 meters deep (Gibbs et al. 1987), and it ranges from flimsy to sturdy (Butler 1992). Nests are often reused from year to year, and may even be "borrowed" by species other than great blue herons, such as Canada geese, house sparrows, and great horned owls (Vermeer 1969). Nests are usually made of dead sticks, but fresh material may be plucked from nearby sources and added to the nest during brooding of chicks. Time invested in building the nest ranges from 3 days to two weeks (Butler 1992). The nest is constructed by the female with materials presented by the male (Cotrille and Cotrille 1958, Palmer 1962, Mock 1976).
Males arrive first at the nest site and court females from the nest (Kaufman 1996, Brandman 1976, Mock 1976). The male may choose a mate from as many as five females. Courtship behavior involves elaborate displays by males, including stretching the neck up with bill pointing skyward, flying in circles above colony with neck extended, stretching the neck forward with head and neck feathers erect and then snapping the bill shut (Kaufman 1996).
The bird breeds in pairs in colonies, often composed entirely of its own species. Often a colony will contain several hundred pairs of birds (Butler 1992). Occasionally great blue herons will breed alongside other species, including other herons, waterfowl, and even hawks, owls, and vultures (Custer et al. 1980, Mengel 1965, Ryser 1985). The heron rarely breeds in isolated pairs (Kaufman 1996).
The great blue heron is monogamous within a particular breeding season but may choose a different mate between years (Butler 1992). In California, the courtship-to-egg-laying period is early January to mid-March (Brandman 1976). Copulation occurs on the nest or very near to it, and is achieved in the morning or evening because females are away from the nests during mid-day (Butler 1992).
One to seven (usually from three to five) pale blue eggs are laid (Kaufman 1996). The mean clutch size reported in a 13-year study of a heronry on the central California coast was 3.16 eggs (+/- 0.04) (Pratt and Winkler 1985). Clutch size varies geographically, with populations at higher latitudes generally producing larger clutches (Palmer 1962, Henny and Bethers 1971, McAloney 1973). Mean clutch size decreases as the season progresses (Pratt et al. 1985). Both males and females share in egg incubation duties (Pratt 1970, Brandman 1976, Mock 1979). Males spend approximately 10.4 hours incubating per day, and females average 3.5 hours per day (Brandman 1976). Females incubate eggs at night (Butler 1992). In California, incubation lasts 25-29 days (Pratt 1970). In southern California, the first brood per season hatches in early March (Brandman 1976).
Both parents feed the young (Kaufman 1996). At first, young eat food regurgitated by parents, but eventually the young eat whole fish dropped onto the floor of the nest. Young are able to fly at approximately 60 days. For an additional approximately three weeks, fledglings return to the nest to be fed by their parents (Kaufman 1996).
Pratt and Winkler (1985) report that of all nests in their 13-year study, a mean of 1.45 (+/-0.06) young were fledged per nest (46.8 percent of all eggs laid). In northern populations, one brood is usually produced per year, while in southern populations, two broods may be produced (Kaufman 1996). Birds may also attempt more than one nest if eggs or chicks are lost early in the season (Pratt 1972).
Survival: Although estimates vary regionally, mortality of great blue herons within the first year of life is estimated at 69.0 percent. Of those surviving the first year, 36.3 percent will perish in the second year. The mortality rate for subsequent years is 21.9 percent (Henny 1972).
Great blue herons may live for 15 years (USFWS 2001). The oldest banded heron survived to an age of 23 years (USFWS 2001).
Dispersal: Most young great blue herons disperse far from the natal colony, and few yearlings return to the natal colony (Henny 1972). Adults disperse from the colony after the breeding season (Gill and Mewaldt 1979, Pratt 1970, Butler 1991). Nest site fidelity is weak (Simpson 1984).
Most populations of great blue herons move southward in the autumn (Butler 1992).
Socio-Spatial Behavior: Parris (1979) and Butler (1991) suggest that home ranges of great blue herons extend within a 30 kilometer radius of the breeding colony. There is no information on territory size. Male herons usually defend feeding territories, while females and juveniles tend to forage in groups and do not defend territories (Butler 1991, Gibbs 1991). At the nesting site, however, both males and females engage in aggressive displays to defend the nest. Most such displays are directed at other great blue herons and egrets.
Community Relationships: Unattended great blue heron eggs are preyed on by crows and ravens (Butler 1989). Nestlings are preyed upon by eagles, raccoons, bears, turkey vultures, and red-tailed hawks (Butler 1992). Chicks are more likely to be lost to starvation than predation, however (Pratt and Winkler 1985). Colony sites are abandoned subsequent to predation on adults (Butler 1991) and nestlings (Kelsall and Simpson 1980, Simpson et al. 1987).
Great blue heron nests are also used by Canada geese, house sparrows, and great horned owls (Vermeer 1969).
Recovery of beaver populations in the U.S. and Canada may benefit great blue heron populations, because beaver activity produces additional wetland habitat valuable to the heron for nesting and foraging (Butler 1992).
Threats to Species
The single largest threat to the heron is the elimination of wetland foraging and nesting habitat through urbanization and agricultural development. Agricultural development also often involves the application of pesticides, such as dioxin, dieldrin, endrin, and, in the past, DDT. Colonies highly contaminated with dioxins show decreased growth and development of young (Hart et al. 1991), and possible reproductive failure (Elliott et al. 1988, 1989). Dieldrin (Ohlendorf et al. 1981), endrin (Ohlendorf et al. 1979), and heavy metals (Short and Cooper 1985) are suspected to be lethal to the great blue heron. When in use, DDT thinned the eggshells of herons but did not appear to lead to a decrease in reproductive success (Pratt 1974). Although great blue herons currently appear to tolerate low levels of pollutants, these chemicals can move through the food chain, accumulate in the tissues of prey and may eventually cause reproductive failure in great blue herons (USFWS 2001). As water quality worsens, numbers of large fish and insects that the heron feeds on also decrease (USFWS 2001).
Urbanization, in addition to the resulting loss of wetland habitat, also poses a threat to the great blue heron. Breeding colonies are very vulnerable to human-related disturbance, especially early in the nesting season (Butler 1992, Kaufman 1996). Heronries have been abandoned due to human disturbance in the form of housing and industrial development (Simpson and Kelsall 1979), water recreation, and highway construction (Ryder et al. 1980). Heronries in Minnesota were found to be located a minimum of 3.3 kilometers from human dwellings and an average of 1.3 kilometers from the nearest road (Mathisen and Richards 1978). Werschkul et al. (1976) found evidence that herons avoid logging areas; in this study of Oregon heronries the mean distance from an inactive nest to a logging operation was 148 meters, and the mean distance from an active nest to a logging operation was 219 meters. Colonies will generally remain active until the site is disrupted by changes in land use (Short and Cooper 1985).
Other adverse management practices include channelization of water courses, "navigational improvements" such as locks and dams and dredging, strip mining, and removal of old trees (Illinois Natural History Survey 2001).
Historically, shooting was a threat to the heron, perhaps because it made a conspicuous and easy target. This rarely occurs today, however (Kaufman, 1996).
Special Biological Considerations
Initially great blue herons occupy the central portion of a stand of trees. However, heron excretia can have an adverse effect on nest trees (Kerns and Howe 1967, Weise 1978), and as these central trees die the colony radiates outward to occupy living trees (Illinois Natural History Survey 2001).
Graber et al. (1978) suggest that the great blue heron may have an association with natural floodplain dynamics. As waters dry up towards the end of summer, food resources are concentrated at the same time that food demands of nestlings reach their peak.
Great blue heron population sizes appear to be regulated largely by weather conditions. Severe winters regulate northern populations (Blus and Henny 1981), and hurricanes regulate Florida populations (Powell et al. 1989). Proximity of wetlands for foraging appears to strongly influence the number of nesting pairs in the heronry, suggesting that food supply also limits population size in this species (Bayer and McMahon 1981, Gibbs et al. 1987). Females may decrease clutch size when food is difficult to find (Pratt 1974). Kaufman (1996) suggests that overall numbers of great blue herons are likely stable, while Illinois Natural History Survey (2001) contests that numbers of this species are decreasing in Illinois.
The USFWS Chesapeake Bay Field Office (2001) recommends protection of wetland foraging sites within 15-20 kilometers of heron colonies to ensure prey availability. In addition, habitat suitability models (Short and Cooper 1985) suggest that the recommended disturbance-free zone around a potential nest site is 250 meters on land or 150 meters on water. Houses, roads, and similar disturbances should not occur within this zone; activities, like dredging, timbering, and mechanized agriculture, should not occur in the exclusion zone from February through August.
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least Bell's vireo (Vireo bellii pusillus)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
least Bell's vireo (Vireo bellii pusillus)
Status:
State: Endangered
Federal: Endangered (Federal Register 51:16482, May 2, 1986); Partners in Flight Priority Bird Species; Species of Management Concern
GROUP DESIGNATION AND RATIONALE
Group 2
The least Bell's vireo is relatively well distributed throughout the MSHCP Plan Area within suitable habitat in the Riverside Lowland and San Jacinto Foothills Bioregions. It has relatively narrow and well documented habitat requirements. It occurs in several areas that appear to be Core Areas including the Prado Basin/Santa Ana River, Temescal Wash (including Alberhill Creek), Mockingbird Canyon, Murrieta Creek, Temecula Creek, Lake Skinner (including Rawson Canyon), Vail Lake, Wilson Creek, and San Timoteo Canyon. Because it is well known for using riparian scrub, forest and woodland, has been well documented for its habitat requirements, occurs within specified and known Bioregions, but has specific locations that are Core Areas, it will require conservation on a landscape level with site specific considerations for Core Areas.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 9,430 acres of suitable habitat including riparian forest, woodland and scrub habitat within the Riverside Lowlands and San Jacinto Foothills Bioregions.
Objective 2
Include within the MSHCP Conservation Area at least 8 Core Areas and interconnecting linkages. Core areas could include the following areas: 1) the Prado Basin/Santa Ana River (9,670 acres); 2) Temescal Wash including Alberhill Creek (includes Subunit 3 of the Temescal Canyon Area Plan plus Proposed Linkage 2 and Proposed Constrained Linage 6; 4,290 acres); 3) Murrieta Creek (Subunit 1 of the Southwest Area Plan; 2,060 acres); 4) Temecula Creek (Subunit 2 of the Southwest Area Plan; 850 acres); 5) Lake Skinner/Diamond Valley Lake area (including Rawson Canyon) (Existing Core C, Proposed Extension of Existing Cores 5, 6, 7; 29,060 acres); 6) Vail Lake (Subunit 3 of the Southwest Area Plan; 12,320 acres; 7) Wilson Valley (Subunit 2 of the REMAP Area Plan; 33,540 acres) and 8) San Timoteo Canyon (Subunit 3 of The Pass Area Plan; 2,290 acres). Each Core Area will include at least 100 meters of undeveloped landscape adjacent to the riparian woodland and scrub habitat where it occurs within the Criteria Area.
Objective 3
Include within the MSHCP Conservation Area additional areas within the Criteria Area identified as important to the least Bell's vireo. This Objective shall be met through implementation of the Riparian/Riverine Areas and Vernal Pools Policy presented in Section 6.1.2 of the MSHCP, Volume I. Wetland mapping assembled as part of that policy shall be reviewed as part of the project review process and if riparian scrub and/or woodland is identified on the wetland maps and the habitat will not be avoided as part of the project, a focused survey for least Bell's vireo shall be conducted by a qualified biologist in accordance with accepted protocol. If survey results are positive, 90 percent of the occupied portions of the property that provide for long-term conservation value for the vireo shall be conserved in a manner consistent with conservation of the vireo. This will involve including 100 meters of undeveloped landscape adjacent to the habitat conserved.
Objective 4
Within the MSHCP Conservation Area, maintain (once every 3 years) the continued use of, and successful reproduction at 75 percent of the known vireo occupied habitat (including any nesting locations identified in the MSHCP Conservation Area in the future). Successful reproduction is defined as a nest which fledged at least one known young.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
For the purpose of the conservation analysis, potential habitat for the least Bell's vireo includes riparian scrub, woodland, and forest habitat. Based on these habitats, the Plan Area supports approximately 12,210 acres of potential habitat for the least Bell's vireo. Table 1 shows the conservation and loss of potential habitat for the least Bell's vireo. Overall, approximately 9,430 acres (77 percent) of potential habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public Lands.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
LEAST BELL'S VIREO
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| Riverside Lowland and San Jacinto Foothills Bioregions | |||||||
| Riparian Scrub, Woodland, and Forest | 12,210 | 3570 | 5860 | 9430 | 180 | 2600 | 2780 |
| TOTAL | 12,210 | 3,570 (29%) |
5,860 (48%) |
9,430 (77%) |
180 (2%) |
2,600 (21%) |
2,780 (23%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
In addition, the Riparian/Riverine Areas and Vernal Pools policy described in Section 6.1.2 of the MSHCP Volume I provides for conservation of wetlands which provide habitat for this species through avoidance and minimization. Mitigation for impacts to wetlands shall be incorporated in accordance with the "No Net Loss" policy of federal and state wetland regulations. The proposed mitigation shall be directly related to the functions and values of the wetland as related to this species and result in equivalent replacement.
As described below under Data Characterization, 28 of the 56 relatively recent point localities within the UCR database have a high precision. Of these 28 point localities, 12 (43 percent) will be inside the Criteria Area and 7 (25 percent) are located within public/quasi-public lands. In addition to the locations recorded in the UCR database, a total of 336 pairs were recorded within the Prado Basin of the MSHCP Plan Area by the USFWS (Pike et al. 2001) and all of these locations will be within Public/Quasi-Public Lands. None (0 percent) of the point locations are in the rural/ mountainous zone. Of the 9 high precision recent points located outside the MSHCP Conservation Area, five are located within suitable habitat including riparian scrub, southern willow scrub, or open water/ reservoir/pond and the balance are located outside suitable habitat areas within existing residential urban/exotic areas, non-native grassland, or Riversidean sage scrub. Conservation of this species will be considered from a landscape perspective, especially in the more western lowlands along the Interstate 15/215 corridor. This is largely due to the fact that the suitable habitat has been well defined and providing additional suitable habitat that is not currently occupied may assist with the recovery of the species.
In addition, there are definable locations for focusing conservation efforts that comprise the Core Areas of the least Bell's vireo including the Prado Basin/Santa Ana River (9,670 acres), Temescal Wash including Alberhill Creek (includes Subunit 3 of the Temescal Canyon Area Plan plus Proposed Linkage 2 and Proposed Constrained Linage 6; 4,290 acres), Murrieta Creek (Subunit 1 of the Southwest Area Plan; 2,060 acres); Temecula Creek (Subunit 2 of the Southwest Area Plan; 850 acres); Lake Skinner/Diamond Valley Lake area (including Rawson Canyon) (Existing Core C, Proposed Extension of Existing Cores 5, 6, 7; 29,060 acres); Vail Lake (Subunit 3 of the Southwest Area Plan; 12,320 acres; Wilson Valley (Subunit 2 of the REMAP Area Plan; 33,540 acres) and San Timoteo Canyon (Subunit 3 of The Pass Area Plan; 2,290 acres). Each Core Area will include at least 100 meters of undeveloped landscape adjacent to the riparian woodland and scrub habitat where it occurs within the Criteria Area. The total acreage conserved within the MSHCP Conservation Area within the Core Areas for the least Bell's vireo is 94,080 acres.
Additional areas within the Criteria Area identified as important to the least Bell's vireo will also be conserved. This additional conservation will be met through implementation of the Riparian/ Riverine Areas and Vernal Pools Policy presented in Section 6.1.2 of the MSHCP, Volume I, and discussed above. Wetland mapping assembled as part of that policy will be reviewed as part of the project review process and if riparian scrub and/or woodland is identified on the wetland maps, a focused survey for least Bell's vireo will be conducted by a qualified biologist in accordance with Wildlife Agencies accepted protocol. If survey results are positive, 90 percent of the occupied portions of the property that provide for long-term conservation value for the vireo will be conserved in a manner consistent with conservation of the vireo. This will involve including 100 meters of undeveloped landscape adjacent to the habitat conserved.
Finally, as identified in Objective 4, the MSHCP Conservation Area will maintain (once every 3 years) the continued use of, and successful reproduction at 75 percent of the known vireo occupied habitat (including nesting locations identified in the MSHCP Conservation Area in the future). Successful reproduction is defined as a nest which fledged at least one known young.
MSHCP Conservation Area Configuration Issues
Several large blocks of habitat supporting or potentially supporting the least Bell's vireo are within the Criteria Area and Public/Quasi-Public designations, including the Prado Basin/ Santa Ana River, Temescal Wash including the Alberhill Creek tributary, Wasson Canyon, Lake Skinner-Diamond Valley Lake, Lake Elsinore, Lake Mathews-Estelle Mountain, the Badlands, San Timoteo Creek, Vail Lake, Wilson Valley, North Peak Conservation lands, Bautista Creek, and Potrero Valley. Other more constrained areas are provided protection by the designation as MSHCP Conservation Area including areas occupied by least Bell's vireo such as Temecula Creek, and Murrieta Creek. Some of the large blocks of habitat have not been mapped as containing least Bell's vireo or drainages with riparian habitat. However, these habitat blocks likely have smaller riparian systems that contain potentially suitable habitat and could be occupied by vireos in the future. As a long-distance migrant, vireos are able to discover and use patches of riparian habitat that have not been documented to be used in the past although they have been thought to prefer to occupy their natal territories. As such, the MSHCP Conservation Area will provide adequate habitat linkages between Core Areas for this species and will include smaller drainages that may support small numbers of the species. The Prado Basin Core Area is linked along the Santa Ana River to San Bernardino and Orange counties. This riparian area is linked to the south by the Temescal Wash to Lake Mathews and Lake Elsinore. Riparian habitat within the Vail Lake area is linked to the Lake Skinner-Diamond Valley Lake area via Rawson Canyon. The Vail Lake area is also linked to the Santa Rosa Plateau and then to the Santa Margarita River by the riparian habitat in Temecula Creek and Murrieta Creek. The Badlands area provides a major habitat block that provides a linkage to Potrero Creek, Lake Perris, San Jacinto Wildlife Area and continuing north into San Bernardino County.
Conservation Summary
In summary, conservation for this species will be achieved by the inclusion of at least 9,430 acres of suitable Conserved Habitat in the MSHCP Conservation Area. Eight of the Core Areas of the least Bell's vireo will be conserved within large blocks of habitat in the MSHCP Conservation Area and additional areas with few or no recorded locations but that contain potential habitat are also conserved in accordance with the wetland policy. The MSHCP has been designed to preserve the very large breeding population within the Prado Basin/Santa Ana River area. Additionally, the small patches of riparian habitat and the sites containing small numbers of vireos are likely to be just as important as the large population sites. These small populations, documented above to be largely preserved are important to prevent further isolation of remaining breeding groups. Wetland mapping assembled as part of the wetland policy shall be reviewed as part of the project review process and if riparian scrub and/or woodland is identified on the wetland maps and cannot be avoided, a focused survey for least Bell's vireo shall be conducted by a qualified biologist in accordance with accepted protocols. If survey results are positive, 90 percent of the occupied portions of the property that provide for long-term conservation value for the vireo shall be conserved in a manner consistent with conservation of the vireo. For the Core Areas and the new areas to be conserved in accordance with Objective 3, conservation of suitable habitat will include 100 meters of undeveloped landscape adjacent to the habitat conserved. Conservation of the least Bell's vireo will provide for the continued use of, and successful reproduction at 75 percent of the known vireo occupied habitat (including any nesting locations identified in the MSHCP Conservation Area in the future).
The population viability analysis conducted by the USFWS as part of the listing package (USFWS 1998) indicated the least Bell's vireo populations exceeded the minimum viable population size with a less than five percent probability of extinction over a 100-year period. The results of zero probability are due to the sizes and growth rates of each population as well as their interconnectedness through dispersal.
INCIDENTAL TAKE
Approximately 2,780 acres of potential habitat for the least Bell's vireo will be outside the Criteria Area and Public/Quasi-Public designations, or about 23 percent of the total potential habitat. It should be noted that wetland habitats located outside the MSHCP Conservation Area, including those present in the Mockingbird Canyon area, will be subject to the Riparian/Riverine Areas and Vernal Pools policy presented in Section 6.1.2 of the MSHCP, Volume I. However, the population of the least Bell's vireo at Mockingbird Canyon is not included in the MSHCP Conservation Area. Of the 9 high precision recent location points located outside the MSHCP Conservation Area, five are located within suitable habitat including riparian scrub, southern willow scrub, or open water/reservoir/pond and the balance are located outside suitable habitat areas within existing residential/urban/exotic areas, non-native grassland, or Riversidean sage scrub.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The UCR location database contains approximately 80 records for the least Bell's vireo within the western Riverside County area dated from 1888 to 1999. Of these records, approximately 56 are recent (dated within the past 10 years) and approximately 28 of these are high precision and can be accurately placed within the MSHCP Plan Area. In addition, a total of 350 territories were recorded within the Prado Basin of the MSHCP Plan Area by the USFWS in 1998 (Pike, 1998, pers. comm.). The habitat types associated with these recent and high precision records, as well as the records from the Prado Basin, include riparian scrub, riparian forest, sage scrub, chaparral, grassland, tamarisk, reservoir and residential. The residential and upland locations may be records that are located within habitat that is small and adjacent to the recorded habitat type or the record may no longer be extant.
Due to the listing of the least Bell's vireo, a moderately large body of literature exists for the species consisting of several refereed journal articles and an extensive amount of non-refereed technical papers. Thorough reviews of the literature for this species and subspecies have been produced (Franzreb 1989; Brown 1993; USFWS 1998). Much of the following discussion is drawn from these reviews and key publications.
Habitat and Habitat Associations
The least Bell's vireo occupies a more restricted nesting habitat than the other subspecies of Bell's vireo as summarized in USFWS (1986). Least Bell's vireos primarily occupy riverine riparian habitats that typically feature dense cover within 1-2 meters of the ground and a dense, stratified canopy. It inhabits low, dense riparian growth along water or along dry parts of intermittent streams. Typically it is associated with southern willow scrub, cottonwood forest, mule fat scrub, sycamore alluvial woodland, coast live oak riparian forest, arroyo willow riparian forest, wild blackberry, or mesquite in desert localities. It uses habitat which is limited to the immediate vicinity of water courses below 1,500 feet elevation in the interior (USFWS 1986; Small 1994). In the coastal portions of southern California, the least Bell's vireo occurs in willows and other low, dense valley foothill riparian habitat and lower portions of canyons and along the western edge of the deserts in desert riparian habitat.
The least Bell's vireo primarily nests in small, remnant segments of vegetation typically dominated by willows and mule fat but may also use a variety of shrubs, trees, and vines. The birds forage in riparian and adjoining chaparral or scrub habitat (Salata 1983). Nests are typically built within one meter of the ground in the fork of willows, wild rosa (Rosa californica), mule fat (Baccharis salicifolia), or other understory vegetation (Franzreb 1989). Cover surrounding nests is moderately open midstory with an overstory of willow, cottonwood, sycamore, or oak. Crown cover is usually more than 50 percent and contains occasional small openings. The most critical structural component to least Bell's vireo breeding habitat is a dense shrub layer at 2 to 10 feet above the ground (Goldwasser 1981; Franzreb 1989). Quantitative measures for least Bell's vireo habitat have been used to developed standards for occupied habitat in coastal San Diego County. These standards are currently used in evaluating habitat restoration projects (e.g., RECON 1989; DUDEK 1999).
During the spring and fall migration, the Bell's vireo occupies a wider range of habitats including coastal sage scrub, riparian and woodland habitats. The winter range of habitats of the Bell's vireo include thornscrub vegetation adjacent to watercourses or in riparian gallery forests along the west coast of north and central Mexico. In southern Mexico and Honduras, tropical deciduous forest and arid tropical scrub along the coast is used (Brown 1993).
Biogeography
The Bell's vireo, consisting of four subspecies, has a widespread occurrence in central and southwestern U.S. and northern Mexico as a breeding bird. It breeds from southern California to southern Nevada, southwestern Utah, northwestern and southern Arizona, southern New Mexico, central and southwestern Texas, eastern Colorado, central Nebraska, central South Dakota, south central North Dakota, southeastern Minnesota, southern Wisconsin, northeastern Illinois, and northwestern Indiana south to northern Baja, southern Sonora, southern Durango, Zacatecas, southern Nuevo Leon, southern Tamalpais, southern and eastern Texas, northwestern Louisiana, Arkansas, southwestern Tennessee, southwestern Kentucky, southern Indiana, and western Ohio (Brown 1993). The winter range is not well known. Generally it appears to winter from southern Baja and southern Sonora south along the west coast of Mexico and Central America to the Honduras and casually to northern Nicaragua. It is also reported from the eastern coast of Central America from Veracruz south to Honduras (Brown 1993).
Zeiner, et al. (1990) summarize the distribution, abundance, and seasonality of the least Bell's vireo within California as follows. Least Bell's vireo was formerly a common and widespread summer resident below about 600 meters (2,000 feet) in western Sierra Nevada, throughout the Sacramento and San Joaquin valleys, and in the coastal valleys and foothills from Santa Clara County south. Also it was common in coastal southern California from Santa Barbara County south, below about 1,200 meters (4,000 feet) east of the Sierra Nevada, in Owens and Benton valleys, along the Mojave River and other streams at the western edge of southeastern deserts, and along the entire length of the Colorado River (Grinnell and Miller 1944). Two subspecies occur in California: V. b. pusillus (range is described below) and V. b. arizonae which is now a rare summer resident along the Colorado River from Needles, San Bernardino County, south to Blythe, Riverside County. Bell's vireo (subspecies uncertain) also breeds in at least two sites along Amargosa River near Tecopa, Inyo County (Garrett and Dunn 1981).
Usually least Bell's vireo arrives from the Mexican wintering areas by end of March to early April, and departs by end of September (Zeiner, et al. 1990). The males precede the females in arrival by a few days and stragglers have been noted post breeding as late as November (USFWS 1998).
The least Bell's vireo, the subject of this species account, was once common, and was the major breeding subspecies in California. It is endemic to California and northern Baja California and is now a rare, local, summer resident. In 1977-78, 67 males or paired individuals were counted at 23 of 65 sites surveyed on the coastal slope of southern California, and 23 at 9 of 18 sites on the desert slope (Goldwasser, et al. 1980, Garrett and Dunn 1981). The least Bell's vireo formerly was found in valley bottom riparian habitats from Tehama County, California southward locally to northwestern Baja, California, Mexico in the south, and as far east as the Owens Valley, Death Valley, and along the Mojave River (Grinnell and Miller 1944). Except for a few outlying pairs, the subspecies is currently restricted to southern California south of the Tehachapi Mountains and northwestern Baja California (Garrett and Dunn 1981). Breeding pairs have been observed in the counties of Monterey, San Benito, Inyo, Santa Barbara, San Bernardino, Ventura, Los Angeles, Orange, Riverside, and San Diego, with the highest concentration in San Diego County along the Santa Margarita River (Small 1994).
Most of the current populations of least Bell's vireo have undergone tremendous growth. Currently available census data indicate that the population in southern California has increased from an estimated 300 pairs in 1986 to an estimate 1,346 pairs in 1996 (USFWS 1998).
Known Populations Within Western Riverside County
Given the ongoing recovery of the species and the large concentration of birds in the western portion of the Plan Area, the least Bell's vireo may be found in suitable habitats nearly throughout the Plan Area. The least Bell's vireo population in the Prado Basin and contiguous (upstream and downstream) reaches of the Santa Ana River is the second largest population of this endangered species within its range. The population within the Prado Basin area has risen from the low of 19 territorial males in 1986 to 249 territorial males in 1996 (Pike, et al. 1996). Approximately 345 least Bell's vireo territories were detected in this area in 1998 (Pike, 1998, pers. comm.). The most recent survey results indicate that a total of 444 territorial males including 336 pairs are present within the area (Pike et al. 2001). Other key population areas of the least Bell's vireo, in addition to the Prado Basin and Santa Ana River, include: Temescal Wash (including Alberhill Creek), Mockingbird Canyon, Murrieta Creek, Temecula Creek, Lake Skinner (including Rawson Canyon), Vail Lake, Wilson Creek, and San Timoteo Canyon.
Other geographic locations that are recorded within the U.C. Riverside database and by the USFWS including: Lake Elsinore, March ARB, Meadowbrook, Canyon Lake, De Luz Creek, Potrero Creek, Bautista Creek, and Reche Canyon (USFWS 1998; USFWS 1999 unpublished data).
Biology
Genetics: The least Bell's vireo is a member of the avian family Vireonidae and is taxonomically similar to crows and Jays (Corvidae), and woodwarblers, tanagers, buntings, and blackbirds (Emberizidae) (Brown 1993). Genetic research has shown that there are large interspecific differences within the genus vireo and suggests that the taxon is polyphyletic (Johnson et al. 1988). A more recent study has shown that despite the presence of several distinct groupings in the vireo, the evolutionary histories provided by gene sequencing were unable to determine whether the group was monophyletic or polyphyletic (Murray et al. 1994). Four different subspecies of Bell's vireo have been recognized based on taxonomy (American Ornithologists' Union 1957) and geographic separation (Hamilton 1962).
Diet and Foraging: Bell's vireo are known to feed primarily on insects and spiders, and rarely on fruit (Chapin 1925). Insects consumed include flying and crawling species including bugs, beetles, bees, wasps, ants, snails, grasshoppers, moths and butterflies (Chapin 1925; Bent 1950; Terres 1980). Feeding behavior largely consists of collecting prey from leaves or in bark crevices while perched or hovering, and less frequently by capturing prey by aerial pursuit (Salata 1983).
For the least Bell's vireo, foraging occurs primarily within willow (Salix spp.) stands or associated riparian vegetation with forays into non-riparian vegetation including chaparral, and oak woodlands later in the breeding season (Gray and Greaves 1984, Salata 1983; Kus and Minor 1989). Least Bell's vireo are known to forage upon a variety of tree and shrub species preferring black willow (Salix gooddingii), arroyo willow (Salix lasiolepis), and mulefat (Baccharis salicifolia). Individuals are known to travel between 3 and 61 meters (mean = 15.5 meters) while foraging, with the majority of these destinations occurring within 30 meters of the edge of riparian vegetation (Kus and Minor 1989). Least Bell's vireo are known to forage in all vertical vegetation layers from 0 to 20 meters but most feeding is concentrated above the ground surface in the lower vegetation layers between 0 to 6 meters (Kus and Minor 1989; Salata 1983).
Daily Activity: The least Bell's vireo exhibits year-round diurnal activity; and is known to be a nocturnal migrant (Brown 1993).
Reproduction: The breeding season for least Bell's vireo is typically mid-March to September (USFWS 1986). During this period least Bell's vireo are known to breed almost exclusively within riparian habitats (USFWS 1998). Nesting sites are typically selected within structurally heterogeneous woodlands, forests and scrubs that support dense vegetation near the ground, and dense horizontally separated vegetation higher up in the canopy (Goldwasser 1981; Gray and Greaves 1984; Salata 1983; RECON 1989). Quantitative and qualitative measures have thus far failed to identify distinguishing features between nest sites and other suitable habitat within a territory (RECON 1988; Hendricks and Reiger 1989; Olsen and Gray 1989). Nests are typically suspended in forked branches of many different riparian species with no clear preference for any particular species (Nolan 1960; Barlow 1962; Goldwasser 1981). Because Salix spp. and mulefat are the typically the most abundant species in vireo habitat these species appear to be most commonly selected for nesting (Goldwasser 1981; Franzreb 1989).
Least Bell's vireo nests are usually placed between 0.9 and 1.5 meters from the ground with a range between 0.2 to 3.6 meters (Goldwasser 1981; Salata 1984; RECON 1988). Females probably select the nesting sites but both genders participate in nest construction (Barlow 1962). Nests appear to only be used once with new ones constructed for failed or successive broods (Greaves 1987).
The clutch size of the least Bell's vireo is between 2 to 5 (typically 3 or 4) eggs which are laid shortly after nest construction (Salata 1984; Kus 1994; USFWS 1998). A typical clutch is incubated by both parents for about 14 days with the young remaining in the nest for another 10-12 days (Pitelka and Koestner 1942; Nolan 1960; Barlow 1962). Fledglings range from established breeding territories, remaining under parental care for several more weeks (USFWS 1998). Least Bell's vireo produce typically only one brood, but additional broods up to four or five have also been reported (Franzreb 1989; USFWS 1998).
Survival: Survival rates measured as average nesting success has been recorded for several large drainages in southern California (USFWS 1998). The average percentage of nests to successfully produce fledglings ranges over several Plan Areas from 46 percent (on the Santa Ana River) to a high of 74 percent (on the west San Luis Rey River) (USFWS 1998). Another measure of reproductive success is the number of fledglings produced per each pair. This measure for sites in southern California over multiple years of study resulted in an average of between 1.8 and 2.5 fledglings per pair (USFWS 1998). Although least Bell's vireo produce a relatively high number of fledglings it is estimated that less than 29 percent of these individuals survive to return to breeding habitat (USFWS 1998).
Beyond one year, survivorship increases averaging approximately 47 percent (Salata 1983; Kus, unpublished data as described in USFWS 1998). Preliminary data has shown 76 percent mortality for least Bell's vireo in the first year after hatching , and approximately 53 percent mortality per year thereafter (Salata 1983, as cited in Brown 1993).
Banding records have documented Bell's vireo that have lived approximately seven years (Klimkiewicz et al. 1983). Maximum life-span is probably longer (Brown 1993). Over two different time periods of the same population, Greaves and Gray (1991) found that only a small percentage of a least Bell's vireo are older than 3-4 years (8 percent and 15 percent).
Dispersal: Additional research is needed over long periods of time to determine dispersal characteristics of least Bell's vireo (USFWS 1998). Fledgling Bell's vireo expand their dispersal distances from about 10 meters the first day to approximately 60 meters several weeks after fledging (Hensley 1950; Nolan 1960, as cited in Brown 1993). This distance has been shown to increase to approximately 1.6 kilometers during the same breeding season (Gray and Greaves 1984). Studies by B. Kus and J. Greaves have provided estimates of extra-watershed dispersal rates and distances for least Bell's vireo, with approximately 20 percent dispersing outside their natal drainages over distances of 130 miles (from unpublished data cited in USFWS 1998). Data collected by Kus also suggests that males are more likely to disperse from their natal sites than females (from unpublished data cited in USFWS 1998).
The literature on the dispersal and status remains unclear. Early data suggested that least Bell's vireo are strongly site tenacious returning to the same site in close proximity to previously occupied territories (Salata 1983; Greaves 1987; 1989). More recent data suggests that least Bell's vireo may change breeding sites and that additional study is needed (Data from B. Kus as summarized in USFWS 1998).
Socio-Spatial Behavior: In Indiana, Nolan (1960) reported a home range for Bell's vireo of 0.8-1.2 hectares (2.0-3.0 acres). In the breeding season, the home range is probably equal to the territory. In Illinois, Pitelka and Koestner (1942) reported 1 pair per 1.2 hectares (3 acres), and Hensley (1950) reported 1 pair per 1.3 hectares (3.1 acres). In Arizona mesquite thickets, Barlow et al. (1970) found 1 pair per 0.8 hectares (2 acres). In Kansas, Barlow (1962) reported the average territory size of 0.5 hectares (1.25 acres), ranging from 0.1-1.3 hectares (0.26 to 3.1 acres).
Male Bell's vireo contest and establish breeding territories (Barlow 1962). Least Bell's vireo territory sizes range from 0.2 to 3.0 hectares (Gray and Greaves 1984; Collins et al. 1989; Newman 1992) with most averaging between 0.3 to 1 hectare (1 to 3 acres) (USFWS 1998). The home range or territory sizes of the least Bell's vireo range from 0.2 to 1.3 hectares (0.5 to 4.0 acres) according to RECON (1989). Territories in Bell's vireo are maintained by threat and physical confrontation early in the breeding season, tapering to vocal warnings later in the season (Barlow 1964).
Community Relationships: Predation is common in least Bell's vireo owing in part to the close proximity between nest and ground (Franzreb 1989; Kus 1994). Nest predation among least Bell's vireo has been reported as high as 45 percent in the San Luis Rey river to as low as 8 percent on the San Diego river (Salata 1983). Additionally, nest parasitism by the brown-headed cowbird is one of the primary threats to successful reproduction in least Bell's vireo (USFWS 1998).
Threats to Species
Intensive surveys for the least Bell's vireo between 1977 and 1985 of virtually all potential breeding habitat were conducted, resulting in occurrences at only 46 of over 150 former localities (Goldwasser 1978; Goldwasser, et al. 1980). Once common, the vireo populations had decreased substantially by the late 1980's (Goldwasser, et al. 1980).
The narrow and limited nature of the habitat of the least Bell's vireo makes the subspecies more susceptible to major population reductions than the other subspecies. No other passerine (perching songbird) species in California is known to have declined as dramatically as the least Bell's vireo (Brown 1993).
The major threats to the species are similar or identical to those for the southwestern willow flycatcher. The following summary has been taken from the final rule for that species due to the succinctness and the elaboration provided for the discussion (USFWS 1995); however, Brown (1993), as identified below, mirrored the discussion of the loss and degradation of habitat for the least Bell's vireo. The threats can be summarized as follows as: the present or threatened destruction, modification, or curtailment of riparian habitat and the nest parasitism by the brown-headed cowbird that affects its productivity (USFWS 1995).
The decline of the least Bell's vireo coincides with the reduction of riparian habitat throughout its range. In the Central Valley, more than 90 percent of the riparian woodland habitat that existed in the period before settlement has been developed and much of the remaining habitat is in a disturbed or degraded condition. Habitat removal or alteration has occurred as the result of a variety of causes, coinciding with the historical and economic development of California. Early exploitation of woodlands occurred as the result of clearing for agricultural land and for fencing, lumber, and fuel. As the human population grew and the intensity of agricultural activity increased, urbanization occurred in central locations, usually within floodplains near permanent watercourses. This resulted in increased land clearing, demand for wood products, and the need for flood-control and irrigation projects.
The least Bell's vireo has been impacted by the loss and degradation of riparian habitats, loss and modification of hydrological and fluvial processes, sand mining, flood control activities (mowing, channelization), ground water withdrawal, mosquito control, infestation of non-native plant species (i.e., giant reed), widespread cowbird parasitism, loss of native habitat buffers, and edge effects from upland development (Brown 1993).
In addition to outright destruction of habitat, riparian woodlands have been degraded from fragmentation. Fragmentation results in the loss of area-sensitive species, the loss of the larger species, the predominance of alien or very common species, and in breeding depression (USFWS 1998).
Brood parasitism by the brown-headed cowbird also threatens the least Bell's vireo. Cowbirds lay their eggs in the nests of other songbirds. The cowbird often removes a number of the host's eggs and replaces them with an equal number of cowbird eggs. Cowbird eggs require a relatively short incubation period thus the young cowbird hatches earlier than the host's eggs. The effects of brood parasitism include reducing nest success rate and egg-to-fledgling rate and delaying successful fledging. A common response to parasitism is abandonment of the nest. The success rate of re-nesting is often reduced and there may be inadequate time to prepare for migration. In California, parasitism rates range from 50 percent to 80 percent, which is considered to be a high parasitism rate (Brown 1993).
Coincident with the conversion of much of the riparian woodlands to agricultural and other uses, has been the extension of the range of the brown-headed cowbird to include the Pacific Coast of north America. The first observations of the cowbird occurred in the early part of the twentieth century and increase in numbers of this species has been as dramatic as the decline in numbers of the least Bell's vireo. Cowbird parasitism rates have been documented for the period from 1986 to 1996 (Pike, et al. 1996). The rates have varied from a high of 57 percent in 1993 to a low of 16 percent in 1987. During this same time period, cowbird trapping was taking place and a total number removed varied from 1068 in 1994 to 513 in 1993. A complicating factor with the parasitism by the cowbird is the predation rates on the nests. The study in Prado Basin showed a low of 19 percent predation in 1988 to a high of 57 percent in 1993. The additive effect of predation plus cowbird parasitism, which results in loss of reproductive output, provides an overall mortality factor of 46 to 98 percent of the nests. Fortunately, in this Plan Area, the overall population increase somewhat compensates for the loss of the nest effort and the overall projected total recruitment of vireo young has steadily increased from the low of 34 in 1986 to the high in 1996 of 410 young.
Special Biological Considerations
Least Bell's vireos are nearly obligate riparian breeders. They appear to be especially dependent on the presence of willows within occupied habitat, although the structure is extremely important, and they are characterized as preferring early successional habitat (USFWS 1998). The vireo tends to establish territories in sites with a particular habitat configuration, including small amounts of aquatic and herbaceous cover, large amounts of shrub and tree cover, and a large proportion of tree cover with shrub understory. In addition, the width of the vegetation belt appears to be important for establishing vireo territories. Two features appear to be essential for a vireo territory: the presence of dense cover within 1 to 2 meters of the ground and a dense, stratified canopy for foraging. Native upland buffers are particularly important in narrow drainages. Those pairs that select areas bordered by coastal sage scrub and grasslands tended to be more successful than those bordered by agricultural and urban areas. Those territories adjoining golf courses, campgrounds, and sand mines had significantly fewer successful pairs than those next to chaparral, coastal scrub oak or grasslands (Franzreb 1989). Least Bell's vireo is known to forage in upland vegetation up to 300 yards from the nest (USFWS 1986).
Vireo nest sites are most frequently located in stands between 5 and 10 years of age (RECON 1988). Even though mature trees are present at many of the sites, the average age of willow vegetation in the immediate vicinity of most nests is between 4 and 7 years. When mature riparian woodland is selected, vireos nest in areas with a substantial robust understory of willows as well as other species. With the available information it is not possible to say conclusively whether the vireo actually prefers vegetation between 5 and 10 years of age or whether its selection merely reflects the availability of vegetation of this age range in the area. The ecosystem dynamics of scouring of vegetation by flooding and river meandering rejuvenates the gallery of otherwise old-age stands which would normally persist. These tall canopy forests would continue to shade and reduce the understory. Consequently, the riparian plant succession appears to be an important influence in maintaining vireo habitat (Franzreb 1989, Goldwasser 1981).
Virtually all least Bell's vireos winter in Mexico. However, details as to habitat use and locations of winter visitors are unknown (Brown 1993).
Adequate corridors and widespread brown-headed cowbird control is necessary for management. Rangewide management of riparian systems (largely to control cowbird parasitism) has resulted in a much reduced parasitism rate, and an increase in the population numbers (Brown 1993).
Selective shooting of cowbirds, relocation of feedlots, dairies, and stables away from riparian areas, and reduction of grazing in riparian areas are also recommended, as well as revegetation of riparian areas to increase the extent of nesting habitat and deter cowbirds (Laymon 1987). The reintroduction of least Bell's vireo, by a capture and release method, to areas within their historical range has been considered but not done (Franzreb 1990).
A primary objective of riparian restoration in California is the creation of habitat for endangered species (Kus 1998). Creating nesting habitat for the least Bell's vireo is feasible and has been documented to occur. Least Bell's vireo visited restoration sites within the first year for foraging purposes. They used the restoration sites as components of their overall territory by incorporating native patches of habitat within the restoration area. Vireos nesting in the restored habitat achieved success comparable to that of vireos nesting in the surrounding natural habitat and there was no evidence that productivity was reduced in the created areas.
Recovery and management efforts should focus on addressing the two major causes of decline of the least Bell's vireo: habitat loss and degradation and brown-headed cowbird nest parasitism. The brown-headed cowbird removal programs have been the most effective short-term management effort. Land uses that perpetuate cowbird foraging in the range of the least Bell's vireo are recommended to be modified for long-term benefits that reduce the need for human intervention. Nest monitoring programs will also be essential to determine the levels of brown-headed cowbird parasitism. To address the habitat aspect of the cause of population decline, the development of management plans will be necessary. The Santa Ana River population of the least Bell's vireo is one of the metapopulations for which a management plan will be required and is located within the Plan Area. Critical habitat for the vireo extends from Rubidoux near Riverside downstream through the Prado Basin. Much of the current habitat in the watershed for the least Bell's vireo is found in Prado Basin. A significant percentage of the woodland habitats are lacking or devoid of well-developed understories and several non-native plant species have invaded substantial portions of the area. Potentially conflicting land uses within the watershed include parks, developments, airport, livestock, oil field, industry, and agriculture. Riparian communities on the Santa Ana River are threatened by water supply projects, exotic species, flood-sediment control and channelization projects, road projects, and sand and gravel mining (USFWS 1998).
LITERATURE CITED
American Ornithologists' Union. 1957. Checklist of North American birds. 5th edition. Lord Baltimore Press, Baltimore, MD. 691 pp.
Barlow, J. C. 1962. Natural History of Bell's Vireo, Vireo bellii Audubon. University of Kansas Publication 12:241-296.
Barlow, J. C. 1964. Swaying display of a female Bell's virwo. Auk 81: 89-90
Bent, A.C. 1950. Life Histories of North American Wagtails, Shrikes, Vireos, and their Allies. U.S. National History Museum Bulletin 197.
Brown, B.T. 1993. Bell's Vireo. In The Birds of North America, No. 34 (A. Poole, P. Stettenheim, and F. Gill, Eds) Philadelphia: The Academy of Natural Sciences; Washington D.C.: The American Ornithologists' Union.
Chapin, E.A. 1925. Food Habits of the Vireos. Bulletin 1355, U.S. Department of Agriculture, Washington D.C.
Collins, C.T., L.R. Hays, M. Wheeler, and D. Willick. 1989. The Status and Management of the Least Bell's Vireo within the Prado Basin, California, 1986-1990. Final Report to Orange County Water District, Fountain Valley, CA.
Dudek and Associates. 1999. 1999 Monitoring Report for the Tijuana River Emergency Channel Project. Prepared for the City of San Diego, CA. 37 pp.
Franzreb, K.E. 1989. Ecology and Conservation of the Endangered Least Bell's Vireo. Biological Report 89(1), U.S. Dept. Of the Interior, USFWS, Sacramento, Calif.
Franzreb, K. E. 1990. An analysis of options for reintroducing a migratory, native passerine, the endangered least Bell's vireo, Vireo bellii pusillus, in the Central Valley, California. Biological conservation 53: 105-124.
Garrett, K., and J. Dunn. 1981. The Birds of Southern California: Status and Distribution. Los Angeles Audubon Society. 408 pp.
Goldwasser, S. 1978. Distribution, reproductive success and impact of nest parasitism by brown-headed cowbirds on least Bell's vireos. Final Report, California Department of Fish and Game, Project W-54-R-10, Job IV 1.5.1.
Goldwasser, S. 1981. Habitat Requirements of the Least Bell's Vireo. Final Report, California Department of Fish and Game, Job IV-38.1. 16pp.
Goldwasser, S., D. Gaines, and S. R. Wilbur. 1980. The least Bell's vireo in California: a de facto endangered race. American birds 34: 742-745.
Gray, M.V., and J. Greaves. 1984. The Riparian Forest as Habitat for the Least Bell's Vireo. Pp. In R. Warner and K. Hendrix, eds. California Riparian Systems: Ecology, Conservation, and Productive Management. University of California Press, Davis CA.
Greaves, J.M. 1987. Nest-site Tenacity of Least Bell's Vireos. Western Birds 18:50-54.
Greaves, J.M. 1989. Maintaining Site Integrity for Breeding Least Bells Vireos. Pp. 293-298 in D. L. Abell, ed. California Riparian Systems Conference: Protection, Management, and restoration for the 1990's; 1988 September 22-24, Davis, CA. Pacific Northwest Forest and Range Experiment Station, Berkeley, CA; USDA Forest Service General Technical Report. PSW-110. 544 pp.
Grinnell, J., and A. H. Miller. 1944. The Distribution of the Birds of California. Pacific Coast Avifauna Number 27. Reprinted by Artemisia Press, Lee Vining, California, 1986. 615pp.
Hamilton, T. 1962. Species Relationships and Adaptations for Sympatry in the Avian Genus Vireo. Condor 64:40-48.
Hendricks, B.J. and J.P. Rieger. 1989. Description of Nesting Habitat for the Least Bell's Vireo in San Diego County. Pp. 285-292 in D. L. Abell, ed. California Riparian Systems Conference: Protection, Management, and restoration for the 1990's; 1988 September 22-24, Davis, CA. Pacific Northwest Forest and Range Experiment Station, Berkeley, CA; USDA Forest Service General Technical Report. PSW-110. 544 pp.
Hensley, M. 1950. Notes on the Breeding Behavior of the Bell's Vireo. Auk 67:243-244.
Johnson, N.K., R.M. Zink, and J.A. Martin. 1988. Genetic Evidence for Relationships in the Avian Family Vireonidae. Condor 90:428-445.
Jones, B. A. 1985. A Report on the Status of the Least Bell's vireo on the San Diego, Sweetwater, and San Luis Rey River, San Diego, CA. 52 pp,
Kus, B.E., and K.L. Miner. 1989. The use of non-riparian habitats by least Bell's vireos (Vireo bellii pusillus) In: D.L. Abell, ed. California Riparian Systems Conference: Protection, Management, and restoration for the 1990's; 1988 September 22-24, Davis, CA. Pacific Northwest Forest and Range Experiment Station, Berkeley, CA; USDA Forest Service General Technical Report. PSW-110. 544 pp.
Kus, B.E. 1994. Breeding Status of the Least Bell's Vireo in the Tijuana River Valley, California, 1994. Unpublished report prepared for the International Boundary and Water Commission. 22 pp.
Kus, B. E. 1998. Use of restored riparian habitat by the endangered least Bell's vireo, Vireo bellii pusillus. Restoration Ecology 6: 75-82.
Laymon, S. A. 1987. Brown-headed cowbirds in California: historical perspectives and management opportunities in riparian habitats. Western Birds 18: 63-70.
Murray, B. W., W. McGillivray, J. C. Barlow, R. N. Beech, and C. Strobeck. 1994. The use of cytochrome B sequence variation in estimation of phylogeny in the Vireonidae. Condor 96: 1037-1054.
Newman, J. 1992. Relationships between territory size, habitat structure and reproductive success in the least Bell's vireo, Vireo bellii pusillus. Unpublished Master's thesis, San Diego State University.
Nolan, V. 1960. Breeding Behavior of the Bell Vireo in southern Indiana. Condor 62:225-244.
Olsen, T.E. and M.V. Grey. 1989. Characteristics of Least Bell's Vireo Nest Sites along the Santa Ynez River. Pp. 278-284 in D. L. Abell, ed. California Riparian Systems Conference: Protection, Management, and restoration for the 1990's; 1988 September 22-24, Davis, CA. Pacific Northwest Forest and Range Experiment Station, Berkeley, CA; USDA Forest Service General Technical Report. PSW-110. 544 pp.
Pike, James. 1998. USFWS. pers. comm.
Pike, J., M. Wheeler, V. Smith, and L. R. Hays. 1996. The status and management of the least Bell's vireo and southwestern willow flycatcher within the Prado Basin, California, 1986-1996. Prepared for the Nature Conservancy and the Orange County Water District, U.S. Army Corps of Engineers, U.S. Fish and Wildlife Service, and California Department of fish and Game.
Pike, J., D. Pellegrini, L. Hays, and R. Zembal. 2001. Least Bell's vireos and southwestern willow flycatchers in Prado Basin of the Santa Ana River watershed, CA. Prepared for the Orange County Water District and U.S. Fish and Wildlife Service. 21 pp.
Pitelka, F., and Koestner. 1942, Breeding Behavior of Bell's Vireo in Illinois. Wilson Bulletin 54:97-106.
RECON (Regional Environmental Consultants). 1988. Draft Least Bell's Vireo Study Program: interim report for Eastside Reservoir Siting Project. Prepared for the Metropolitan Water District.1989.
RECON (Regional Environmental Consultants). 1989. Comprehensive Species Management Plan for the Least Bell's Vireo. Prepared for the San Diego Association of Governments.
Salata, L. 1983. Status of the least Bell's Vireo on Camp Pendleton, California: report on research done in 1983. Unpubl. Rept., U.S. USFWS, Laguna Niguel, California. 63 pp.
Salata, L. 1984. Status of the least Bell's vireo on Camp Pendleton, California: report on research done in 1984. Unpubl. Rept., U.S. USFWS, Laguna Niguel, California. 54 pp.
Small, A. 1994. California Birds: Their Status and Distribution. Ibis Publishing Company: Vista, CA. 342 pp.
Terres, J. K. 1980. The Audubon Society Encyclopedia of North American Birds. Alfred A. Knopf, New York, New York. 1109pp.
U.S. Fish and Wildlife Service. 1986. Endangered and threatened wildlife and plants; determination of endangered status for the least Bell's vireo. Final Rule. Federal Register 51: 16474-16482.
U.S. Fish and Wildlife Service. 1995. Endangered and Threatened Wildlife and Plants; Final Rule Determining Endangered Status for the Southwestern Willow Flycatcher. Federal Register 60:10694-10715.
U.S. Fish and Wildlife Service. 1998. Draft Recovery Plan for the Least Bell's Vireo (Vireo bellii pusillus). United States Fish and Wildlife Service, Region 1, Portland, Oregon.
U.S. Fish and Wildlife Service. 1999. Unpublished data.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
Lincoln's sparrow (Melospiza lincolnii)- breeding
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
Lincoln's sparrow (Melospiza lincolnii)- breeding
Status:
State: None
Federal: None
GROUP DESIGNATION AND RATIONALE
Group 1
The Lincoln's sparrow has a sparse and widespread distribution throughout the MSHCP Plan Area within a wide variety of habitats. It occurs within the lowland and foothills Bioregions of the Plan Area as a transient in the spring and fall and may winter within the area. Although there are few documented records of the species it has been reported as common within the lowland and foothills areas as a winter transient and migrant in a variety of Habitats.
Because it is widespread as a wintering bird within the Plan Area and population levels rangewide appear to be stable, it is anticipated that this species will respond well to a landscape level of management for its wintering occurrence within the Plan Area.
Lincoln's sparrow is a rare breeder in the Plan Area within the mountain Bioregions. There are approximately 1,050 acres of montane riparian and wet meadow in the Plan Area. Approximately, 470 of these would be included in the MSHCP Conservation Area. Because Lincoln's sparrow nesting habitat is very restricted in the Plan Area, 55 percent of it would be lost, and there is no information about the relative use or importance of the conserved habitat versus the unconserved Habitat, Incidental Take of nesting Lincoln's sparrow is not included in this permit until conservation of the species in the Plan Area has been demonstrated by reaching Objective 3 below.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 470 acres of suitable breeding habitat including montane riparian, riparian scrub and wet meadow within the San Bernardino Mountains and San Jacinto Mountains Bioregions.
Objective 2
Include within the MSHCP Conservation Area 190,390 acres of suitable wintering habitat including chaparral, coastal sage scrub, grassland, freshwater marsh, Peninsular juniper woodland, riparian scrub, woodland, and forest, oak woodland and forest, and Riversidean alluvial fan sage scrub in Riverside Lowland and San Jacinto Foothills Bioregions.
Objective 3
Within the MSHCP Conservation Area, maintain occupancy within 3 large Core Areas (100 percent) in at least 1 year out of any 5 consecutive-year period. In order for this species to become a Covered Species Adequately Conserved, the following conservation must be demonstrated: Include within the MSHCP Conservation Area at least 100 acres in 3 Core Areas. Core Areas may include the following: (1) Tahquitz Valley; (2) Round Valley; (3) Garner Valley. The three Core Areas will be large, consisting of a minimum of 50 acres of montane meadow, wet montane meadow, and edges of montane riparian or riparian scrub. The Core Areas will be demonstrated to support at least 20 Lincoln's sparrow pairs with evidence of successful reproduction within the first 5 years after permit issuance. Successful reproduction is defined as a nest which fledged at least one known young.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
For the purpose of the conservation analysis, potential breeding habitat for the Lincoln's sparrow includes montane meadow and wet montane meadow and the edges of montane riparian or riparian scrub to provide perching opportunities. These habitat types provide foraging habitat during the breeding season as well as the necessary nesting sites. Wintering and migratory areas include lowland shrub and scrub habitats (chaparral, coastal sage scrub, grassland, freshwater marsh, Peninsular juniper woodland, riparian scrub, woodland, and forest, oak woodland and forest, and Riversidean alluvial fan sage scrub) and locations have been described below. Based on these known breeding and wintering habitats, the Plan Area supports approximately 1,050 acres of potential breeding habitat and 410,060 acres of potential wintering habitat for the Lincoln's sparrow. Table 1 shows the conservation and loss of potential habitat for the Lincoln's sparrow. Overall, approximately 470 acres (45 percent) of potential breeding habitat and 190,390 acres (46 percent) of potential wintering habitat will be conserved in Criteria Area or existing Public/Quasi-Public lands.
The Lincoln's sparrow nests within montane meadows, and montane riparian habitats within Forest Service lands. Under the existing Forest Land allocation plan, these locations or habitats generally are within the San Jacinto wilderness areas as well as in most of the grazing allotments.
The Riparian/Riverine Areas and Vernal Pools policy described in Section 6.1.2 (MSHCP Volume 1) provides for conservation of wetlands, including riparian habitat and wet meadows which may be potential nesting areas and which provide habitat for this species. This conservation of wetlands is through avoidance and minimization. Mitigation for impacts to wetlands shall be incorporated in accordance with the "No Net Loss" policy of federal and state wetland regulations. The proposed mitigation shall be directly related to the functions and values of the wetland as related to this species and result in equivalent replacement. Thus, although little meadow habitat is proposed for conservation within Criteria Area or Public/Quasi-Public categories, wetland regulations will provide for avoidance, minimization and at least equivalent replacement of the wetland functions and value related to the Lincoln's sparrow.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
LINCOLN'S SPARROW
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| Breeding Habitat within San Bernardino Mountains and San Jacinto Mountains Bioregions | |||||||
| Meadow | 490 | 0 | 80 | 80 | 20 | 390 | 410 |
| Montane Riparian, Riparian Scrub | 560 | 70 | 320 | 390 | 10 | 160 | 170 |
| Subtotal Breeding Habitat | 1,050 | 70 (7%) |
400 (38%) |
470 (45%) |
30 (3%) |
550 (52%) |
580 (55%) |
| Wintering habitat in Riverside Lowlands and San Jacinto Foothills Bioregions | |||||||
| Chaparral | 132,080 | 45,820 | 24,170 | 69,990 | 30,760 | 31,330 | 62,090 |
| Coastal Sage Scrub | 133,110 | 43,690 | 27,200 | 70,890 | 19,740 | 42,480 | 62,220 |
| Grassland | 121,750 | 17,470 | 16,130 | 33,600 | 7,000 | 81,150 | 88,150 |
| Freshwater Marsh | 470 | 170 | 240 | 410 | 0 | 60 | 60 |
| Pennisular Juniper Woodland | 930 | 340 | 180 | 520 | 0 | 410 | 410 |
| Riparian scrub, woodland and forest | 12,210 | 3,570 | 5,860 | 9,430 | 180 | 2,600 | 2,780 |
| Oak Woodland and Forest | 4,080 | 1,020 | 510 | 1,630 | 920 | 1,630 | 2,550 |
| Riversidean alluvial Fan Sage Scrub | 5,430 | 2,710 | 1,310 | 4,020 | 160 | 1,250 | 1,410 |
| Subtotal Wintering Habitat | 410,060 | 114,790 | 75,600 | 190,390 | 58,760 | 160,910 | 219,670 |
| TOTAL | 411,110 | 114,860 (28%) |
76,000 (18%) |
190,860 (46%) |
58,790 (14%) |
161,460 (39%) |
220,250 (54%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
As described below under Data Characterization, 48 of the 71 relatively recent point localities have high precision. Of these 48 point localities, 13 will be inside the Criteria Area or Public/Quasi-Public lands. However, these data locations, as described above, are for wintering or migratory individuals and do not represent breeding birds. Breeding locations have not been documented other than qualitatively for the Tahquitz and Round valleys which are located within the Mt. San Jacinto State Park and the Mt. San Jacinto Wilderness Area. These locations will be conserved. Thus, the documented breeding locations are located within Criteria Area or Public/Quasi-Public areas. Conservation of this species should be considered from a landscape perspective for nesting due to the fact that the suitable habitat has been well defined. Conserving additional suitable habitat that is not currently occupied may assist with the recovery of the species. There are definable montane meadow locations for focusing conservation efforts within the San Bernardino National Forest lands.
MSHCP Conservation Area Configuration Issues
Several large blocks of habitat supporting or potentially supporting Lincoln's sparrow nesting will be conserved as Criteria Area and public/quasi public designations, including the wilderness areas within the San Bernardino National Forest and the Mt. San Jacinto State Park. Other areas that provide winter and migratory stopover habitat also are provided within the MSHCP Plan Area. Wintering areas may be as important for the species as the breeding areas and these include: Prado Basin, Lake Mathews-Estelle Mountain Reserve, Wasson Canyon, Santa Ana River, Santa Rosa Plateau Temecula and Murrieta creeks, Lake Skinner, Vail Lake, Lakeview Mountains, Wilson Valley, Lake Perris, and Mystic Lake/San Jacinto Wildlife Area. Some of the large blocks of habitat, such as the Badlands and Agua Tibia Wilderness Area have not been mapped as containing Lincoln's sparrows. However, these habitat blocks may have suitable foraging habitat for winter and migration. As such, the MSHCP Conservation Area will provide well-protected nesting areas, which are of limited extent within montane regions. In addition, the Criteria Area and Public/Quasi-Public lands will provide adequate foraging and migratory stopover habitat for the non-breeding season.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 470 acres of suitable Conserved Habitat for breeding and 190,390 acres of suitable Conserved Habitat for wintering. Incidental Take of nesting Lincoln's sparrow is not included in this permit until conservation of the species in the Plan Area has been demonstrated by reaching Objective 2.
INCIDENTAL TAKE
The Incidental Take of the Lincoln's sparrow is difficult to quantify due to our limited knowledge of its distribution and abundance within the Plan Area. The maximum level of Incidental Take of Lincoln's sparrow can be anticipated by the loss of the number of acres of habitat that will become unsuitable for this species. About 580 acres (55 percent) of potential breeding habitat for the Lincoln's sparrow will be outside the Criteria Area and Public/Quasi-Public lands, and individuals within this habitat will be subject to Incidental Take consistent with the Plan upon satisfaction of Objective 2 above. Of this area, approximately 30 acres (3 percent) will be within Rural/ Mountainous designation areas. Although these areas will not be part of the managed MSHCP Conservation Area and the existing zoning/ordinances for these areas do not preclude development and could allow substantial fragmentation and/or degradation of habitat for proposed covered species, the anticipated levels of development in these areas may be consistent with the continued presence of the Lincoln's sparrow, although Lincoln's sparrow tends to be of insular distribution for nesting and thus may be sensitive to fragmentation of its suitable breeding habitat. Take of nests of Lincoln's sparrow is not covered by the MSHCP Plan. About 219,670 acres (54 percent) of potential wintering habitat for the Lincoln's sparrow will be outside the Criteria Area and Public/Quasi-Public Lands and individuals within this habitat will be subject to Incidental Take consistent with the Plan.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The location database for the Lincoln's sparrow includes approximately 80 records dated from 1887 to 1999. Of the more recent records, of which 71 are dated from 1990 to present, there are approximately 48 records that have high precision and may be accurately located within the Plan Area. Most of these high precision and recent records are located within sage scrub, open water, agriculture, woodland, residential, riparian, or non-native grassland habitats and are located in the low elevation areas. These data locations reflect migratory or wintering individuals. Only one record is located in the higher elevation areas within conifer forest and represents a potential breeding location. If the location was a breeding location, it was likely located at the edge of the coniferous forest habitat within or near a meadow or seep.
A low-to-moderate amount of literature is available for the Lincoln's sparrow, mostly relating to general natural history and the Melospiza sparrows in general. Few controlled scientific studies have been conducted and little management information is available. Very little information is available for the Plan Area other than what is available regarding basic distribution information.
Habitat and Habitat Associations
Lincoln's sparrow is known to prefer dense, low underbrush often in disturbed edges with grasses and weeds mixed with shrubs (Bent 1968). The species occurs in a variety of habitats including willow-sedge swamp, scrub-meadow and flat land aspen (Salt 1957). Breeding in southern California occurs in wet montane meadows of corn lily, sedges and low willows (Garrett and Dunn 1981). Lincoln's sparrows are most common in wet meadows with little damage by grazing; singing males are concentrated in flooded or boggy areas near meadow edges where pines provide elevated perches for singing and patches of willows are often present nearby (Cicero 1997). At lower elevations, it prefers mesic willow shrubs and can be found in mixed deciduous groves such as aspen and cottonwoods, mixed shrub-willows, bogs as well as a variety of other riparian habitats (Ammon 1995). It is sometimes reported using forest clear cuts, but usually only near bogs. It generally avoids openings without shrub cover. Its primary microhabitat use includes low willows for nesting, the ground and base of willows for foraging, and tall trees and exposed willow branches for singing (Ammon 1995).
During the winter and spring and fall migration, the species requires thickets of shrubs or tall forbs interspersed with grassy areas, usually on damp ground or near water (Zeiner, et al. 1990). It uses lowlands that are avoided during the breeding season. It may be found in the urban and suburban environment. It is also found in brushy forest edges, weedy fields, hedgerows, marshes, and blackberry thickets. For wintering, its primary habitats in Mexico include tropical evergreen forest, arid and humid pine-oak forests, tropical deciduous forest, Pacific swamp forest, and arid subtropical scrub. It also inhabits savannah, freshwater marsh, and coniferous forests (Ammon 1995).
Biogeography
The Lincoln's sparrow is found during the summer in Alaska, all of Canada, northern U.S. and mountains of the West (Terres 1980). More specifically, it has a boreal distribution from west-central Alaska, central Yukon, central northwest territories, northern Saskatchewan and northern Manitoba to north central Quebec, Labrador, and Newfoundland, south through the Cascade Mountains of Washington, Oregon, and California to southern Tulare County; also south through Wyoming, central and western Colorado to south central New Mexico and west to northeast Utah and north central Idaho (Ammon 1995). In Oregon, it also breeds in the Blue Mountains and Wallowa Mountains; in California, it also breeds in the Warner Mountains, the northern inner coastal range south to Tehama County, in the San Bernardino Mountains, and irregularly in other mountain ranges of the southwest (Ammon 1995).
Wintering for the species occurs along the Pacific coast of British Columbia, Washington, Oregon and California, in the central part of the United States, in Baja California, Mexico, along the Gulf Coast and it is a causal wintering bird in Central America (Ammon 1995; Terres 1980). The species is a common migrant and winter visitor throughout the state with some breeding populations in the northern mountains (Zeiner, et al. 1990). Individuals arrive in southern California in late September and depart in late April (Unitt 1984).
No historical changes in distribution boundaries are known (Ammon 1995). Between 1966 and 1991, there have been significant increases in the breeding populations in Alberta, New Brunswick, northern spruce-hardwood forests, aspen parklands, and the central Rocky Mountains. When measured overall ( the entire North American continent), the population increases were also significant for the period 1966 to 1991. Between 1982 and 1991, the breeding populations in Quebec and the northern spruce-hardwood forests decreased but increased in British Columbia. Several new populations have been documented to be established in the Tulare County area of California probably as a result of wetland establishment (Ammon 1995).
Known Populations Within Western Riverside County
Lincoln's sparrow occurs within the western Riverside County area as a migrant and winter visitor throughout the lowland areas and is fairly common to locally common in overgrown fields and brush thickets and channels (Garrett and Dunn 1981). Locations within the UCR database that are either migrant or wintering individuals include the following areas within the central portion of the Plan Area: Prado Basin, Lake Mathews area, Wasson Canyon, Santa Ana River, Santa Rosa Plateau, Temecula/Murrieta area, Lake Skinner, Vail Lake, Lakeview Mountains, Wilson Valley, Lake Perris, and Mystic Lake/San Jacinto Wildlife Area. It is a summer breeding bird within the San Bernardino Mountains and San Jacinto Mountains in Tahquitz and Round valleys although there are no location records within the UCR database specified as breeding locations (Zeiner, et al. 1990; Garrett and Dunn 1981).
Biology
Genetics: Studies of allozyme, mitochondrial DNA and morphometric variation in sparrows revealed the consensus phylogenetic tree pattern to be (Song sparrow [swamp sparrow, Lincoln's sparrow]) (Zink and Blackwell 1996). Due to the similarities in juvenal plumages, the Lincoln's sparrow is sometimes placed in the genera Passerella or Zonotrichia (Graber 1955).
Diet and Foraging: The Lincoln's sparrow forages on seeds and insects (Zeiner, et al. 1990). Animal foods predominate in breeding season; seeds are the main foods at other times (Martin, et al. 1961). The members of the Coleoptera ranked highest for preference and of the non-Coleoptera, selections tended to be for cryptic and uniformly distributed insects (Raley and Anderson 1990). It often scratches for food in the soil and leaf litter and occasionally hawks insects in the air (Zeiner, et al. 1990). During winter and migration, it forages in cultivated fields, park like structures, riparian vegetation, roadsides and usually forages on the ground. During the breeding season, it forages on the ground in willow bogs, lower parts of willows, coniferous trees, but mostly in dense underbrush or ground vegetation (Ammon 1995).
Daily Activity: Lincoln's sparrow is a year-long diurnally active species (Zeiner, et al. 1990). It generally migrates at night (Ammon 1995).
Reproduction: Nesting of the Lincoln's sparrow occurs on the ground usually in a shallow depression often at the base of a willow and is located within wet meadows with willow thickets (Zeiner, et al. 1990). The species is a solitary, monogamous nester and the nest is typically extremely difficult to find (Bent 1968). The nest has a distinct nest entrance tunnel through the ground vegetation, oriented toward the east-northeast. The clutch size is 3-6 eggs usually 4 or 5 eggs and it may be double-brooded (Zeiner, et al. 1990). It probably breeds first at one year (Harrison 1978).
Survival: The number of young Lincoln's sparrow fledged per egg laid varies between years from 34 percent to 62 percent depending on predation rates, nestling starvation, and exposure (Ammon 1995). The average adult survivorship is unknown but it can reach at least seven years (Klimkiewicz and Futcher 1987).
Dispersal: High dispersal rates for juveniles of the Lincoln's sparrow is noted by one source (Ammon 1995). Only 2 percent of the young are known to return to the natal site. Return rates to the established breeding grounds from year to year is 37 percent for males and 36 percent for females (Ammon 1995).
Socio-Spatial Behavior: Territory size of Lincoln's sparrow during the breeding season is thought to be about one acre (Zeiner, et al. 1990; Terres 1980). The Lincoln's sparrow is characterized by a low population density, a low, constant territorial defense rate, and a large number of concurrently overlapping territories (Wortman-Wunder 1997). Territory boundaries are easily defined because territorial males generally use conspicuous trees and shrubs as singing perches. Territory sizes vary substantially among locations, from an estimated diameter of 35 meters in high-density populations to more than 100 meters in lower density populations. The Lincoln's sparrow uses the territory primarily for nesting and it often forages outside the territory. Territorial boundaries break down about 5 to 8 days after the young fledge as the family group begins to forage throughout the site (Ammon 1995).
In the nonbreeding season, the Lincoln's sparrow is usually solitary or in loose, small foraging flocks of a few individuals. It occasionally mixes with other sparrows, such as white-crowned, song, and swamp sparrows (Ammon 1995).
Community Relationships: Lincoln's sparrow is dominated by and may compete with song sparrows if the breeding territory overlaps (Zeiner, et al. 1990; Cicero 1997).
Threats to Species
Breeding activity of the Lincoln's sparrow was shown to be significantly reduced when a glyphosate-based herbicide was applied to an area in Maine (Ammon 1995; Mackinnon and Freedman 1993). Other threats cited include degradation of breeding habitat via livestock grazing and human disturbance of nest sites (Ammon 1995). Lincoln's sparrows breeding in montane meadows are potentially vulnerable to local extirpation because of their insular distribution, low population density, and fluctuating habitat conditions (Cicero 1997). Heavy damage from livestock grazing drastically increases the probability of local extirpation (Cicero 1997). Based on geographic range, population size, reproductive potential, migratory status, and diet specialization, the Lincoln's sparrow was listed as moderately vulnerable to extirpation as a montane breeding bird in the Great Basin (Reed 1995). Lincoln's sparrow is a rare host to brown-headed cowbirds which is probably due to the lack of overlap of habitat (Ammon 1995).
Special Biological Considerations
All populations are thought to be migratory although summer and winter ranges overlap in central New Mexico and northern California (Ammon 1995). Lincoln's sparrow showed higher densities in post-harvest stands than in post wild-fire stands possibly due to the greater abundance, after harvest, of larger live residual trees and a taller and more dense shrub layer (Hobson and Schieck 1999). In contrast, the studies of Schulte and Niemi (1998) showed the Lincoln's sparrow abundance to be greater in burned areas than in logged forests which was thought to be related to burned areas containing higher densities of dead trees, wider size ranges of dead trees, and greater heterogeneity in the shrub layer than in logged areas. Studies of post-fire events and recovery show that Lincoln's sparrow appears after the falling of dead trees, approximately 15 years after fire and then disappear progressively as the forest matures from shrubs to trees (Crete et al. 1995).
Management should primarily target habitat preservation on both breeding and wintering grounds. Detrimental impacts of habitat alteration on the breeding populations from activities such as livestock grazing probably are related to the species' habitat specialization (Ammon 1995; Knopf et al. 1988; Schulz and Leininger 1991). Maintenance of riparian vegetation in and around montane meadows is important for this species. Surface water diversion, groundwater extraction, heavy recreation use, facilities development, and overgrazing by livestock can degrade the montane riparian habitat (Stephenson and Calcarone 1999).
LITERATURE CITED
Ammon, E. M. 1995. Lincoln's sparrow (Melospiza lincolnii). In The Birds of North America, No. 191 (A. Poole and F. Gill, eds.). The Academy of Natural Sciences, Philadelphia, and The American Ornithologists' Union, Washington, D.C.
Bent, A. C. 1968. Life histories of North American cardinals, grosbeaks, buntings, towhees, finches, sparrows and allies. 3 Parts. U.S. Natl. Mus. Bull. 237. 1889 pp.
Cicero, C. 1997. Boggy meadows, livestock grazing, and interspecific interactions: influences on the insular distribution of montane Lincoln's sparrows (Melospiza lincolnii alticola). Great Basin Naturalist 57: 104-115.
Crete, M., B. Drolet, J. Huot, M. Fortin, and G. J. Doucet. 1995. Post-fire stages of mammal and bird diversity in the north of Quebecois boreal forest. Canadian Journal of Forest Research 25: 150.
Garrett, K. and J. Dunn. 1981. Birds of southern California. Los Angeles Audubon Society. 408pp.
Graber, R. R. 1955. Taxonomic and adaptive features of the juvenal plumage in North American sparrows. Ph.D. diss. Univ. Of Oklahoma, Norman.
Harrison, C. 1978. A field guide to the nests, eggs and nestlings of North American birds. W. Collins Sons and Co., Cleveland Ohio. 416 pp.
Hobson, K. A., and J. Schieck. 1999. Changes in bird communities in boreal mixed wood forest: harvest and wildlife effects over 30 years. Ecological applications 9: 849-863.
Klimkiewicz, M. K., and A. G. Futcher. 1987. Longevity records of North American birds: Coerebinae through Estrilididae. J. Field Ornithology 58: 318-333.
Knopf, F. L., J. A. Sedgwick, and R. W. Cannon. 1988. Guild structure of a riparian avifauna relative to seasonal cattle grazing. J. Wildlife Management 52: 280-290.
MacKinnon, D. S., and B. Freedman. 1993. Effects of silvicultural use of the herbicide glyphosate on breeding birds of regenerating clear cuts in Nova Scotia, Canada. J. Applied Ecology 30: 395-406.
Martin, A. C., H. S. Zim, and A. L. Nelson. 1961. American wildlife and plants, a guide to wildlife food habits. Dover Publ., Inc. New York. 500 pp.
Miller, A. H. and R. C. Stebbins. 1964. The lives of desert animals in Joshua Tree National Monument. University of California Press, Berkeley. 452pp.
Raley, C. M., and S. H. Anderson. 1990. Availability and use of arthropod food resources by Wilson's warblers and Lincoln's sparrows in southeastern Wyoming. Condor 92: 141-150.
Reed, J. M. 1995. Relative vulnerability of extirpation of montane breeding birds in the Great Basin. Great Basin Naturalist 55: 342-350.
Salt, G. W. 1957. An analysis of avifaunas in the Teton Mountains and Jackson Hole, Wyoming. Condor 59:373-393.
Schulte, L. A., and G. J. Niemi. 1998. Bird communities of early-successional burned and logged forest. J. Wildlife Management 62: 1418-1429.
Schulz, T. T., and W. C. Leininger. 1991. Nongame wildlife communities in grazed and ungrazed montane riparian sites. Great Basin Naturalist 51: 286-292.
Terres, J. K. 1980. The Audubon Society Encyclopedia of North American Birds. Alfred A. Knopf, New York, New York. 1109pp.
Stephenson, J. R. and G. M. Calcarone. 1999. Southern California mountains and foothills assessment: habitat and species conservation issues. General Technical Report GTR-PSW-172. Albany, CA: Pacific Southwest Research Station, Forest Service, U.S. Department of Agriculture. 402 pp.
Unitt, P. 1984. The birds of San Diego County. San Diego Society of Natural History: Memoir 13, San Diego, California. 276pp.
Wortman-Wunder, E. 1997. Territory size in Lincoln's sparrows (Melospiza lincolnii). Southwestern Naturalist 42: 446-453.
Zeiner, D.C., W. F. Laudenslayer, K. E. Mayer and M. White eds. 1990. California's Wildlife: Volume II - Birds. California Department of Fish and Game. Sacramento, California. 732pp.
Zink, R. M, and R. C. Blackwell. 1996. Patterns of allozyme, mitochondrial DNA, and morphometric variation in four sparrow genera. Auk 113: 59-67.
loggerhead shrike (Lanius ludovicianus)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
loggerhead shrike (Lanius ludovicianus)
Status:
State: Species of Special Concern
Federal: Federal Special Concern species; Fish and Wildlife Service Migratory Nongame Birds of Management (subspecies mearnsi Endangered)
Other: Audubon Society California Watch List
GROUP DESIGNATION AND RATIONALE
Group 2
The loggerhead shrike is widely but patchily distributed throughout lower elevations of the Plan Area within suitable habitat. Habitat requirements of the loggerhead shrike are known to include open sparse vegetation for foraging and trees and shrubs for nesting. Core areas include the Prado Basin/Santa Ana River, Lake Mathews-Estelle Mountain, Wasson Canyon, Wildomar, Temecula Creek, Wilson Valley, Quail Valley, San Jacinto, Lake Perris/Mystic Lake/San Jacinto Wildlife Area, Moreno Valley, Badlands, and scattered within the larger area of Homeland/Winchester/ Menifee area. Given these well known habitat requirements and specific locations that are considered Core Areas, it is anticipated that this species will respond to a landscape level of management with site specific requirements.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 167,590 acres of suitable foraging and nesting habitat for the loggerhead shrike including agriculture, grassland, cismontane alkali marsh, playa and vernal pool, desert scrubs, Riversidean alluvial fan sage scrub, coastal sage scrub, peninsular juniper woodland and scrub, riparian scrub, woodland and forest, and oak woodlands and forest.
Objective 2
Include within the MSHCP Conservation Area at least 8 of 12 breeding and foraging locations constituting Core Areas including Prado Basin/Santa Ana River (9,670 acres), Lake Mathews-Estelle Mountain area (Existing Core C plus Proposed Extended Existing Core 2; 23,710 acres), Wasson Canyon (Subunit 5 of the Elsinore Area Plan; 2,320 acres), Temecula Creek (Subunit 2 of the Southwest Area Plan; 850 acres), Wilson Valley (Subunit 2 of the REMAP Area Plan; 33,540 acres), Quail Valley (Proposed Linkage 7; 3,400 acres), Lake Perris/Mystic Lake/San Jacinto Wildlife Area (Existing Core H; 17,470 acres), and Badlands (Proposed Core 3; 24,920 acres).
Objective 3
Within the MSHCP Conservation Area, maintain (once every 8 years) the continued use of, and successful reproduction within, 75 percent of the Core Areas. Successful reproduction is defined as a nest which fledged at least one known young.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
The loggerhead shrike uses sparse trees, open woodland, and riparian habitat for nesting and may use a wide variety of habitats, including agriculture lands and grasslands and shrub and scrub habitats for foraging (Garrett and Dunn 1981). Because they will opportunistically use a relatively wide variety of habitats for various parts of their life history, a wide range of habitats has been included for this analysis. For the purpose of the conservation analysis, potential habitat for the loggerhead shrike includes the following habitats within the Riverside lowlands, San Jacinto Foothills, and Santa Ana Mountains Bioregions: agriculture, grassland, cismontane alkali marsh, playa and vernal pool, desert scrubs, Riversidean alluvial fan sage scrub, coastal sage scrub, peninsular juniper woodland and scrub, riparian scrub, woodland and forest, and oak woodland and forest. Although riparian habitat and oak woodland and forest may not typify the sparse habitat that they prefer, many current locations for the species are within such habitats especially within the Santa Rosa Plateau and along the Santa Ana River as well as within other drainages. These locations may be used for nesting. They have been recorded within chaparral, however the number of recorded observations within such a habitat is very low compared to the number of acres of this habitat present within the Plan Area. Thus chaparral has not been included within the conservation analysis although this habitat may contain a limited number of loggerhead shrike nest locations and foraging opportunities within the lower elevation and sparser forms of the habitat. Their nesting habitat, which may be different from the foraging habitat, is composed of habitat with trees such as riparian, oak woodland and forest, and the Peninsular juniper woodland and scrub. Based on these habitats, the Plan Area supports approximately 486,130 acres of habitat for the loggerhead shrike. Table 1 shows the conservation and loss of potential habitat for the loggerhead shrike. Overall, approximately 167,590 (34 percent) of potential habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public Lands. Additionally, 67 percent of riparian or oak woodland and forest habitat with trees for nesting sites, will be conserved.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
LOGGERHEAD SHRIKE
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area (Acres)1 | Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| Agriculture Land | 162,940 | 8,230 | 11,390 | 19,620 | 7,270 | 136,050 | 143,320 |
| Grassland | 132,040 | 18,220 | 20,470 | 38,690 | 11,330 | 82,020 | 93,350 |
| Cismontane Alkali Marsh | 10 | 10 | 0 | 10 | 0 | 0 | 0 |
| Playas and Vernal Pools | 7,910 | 3,830 | 2,920 | 6,750 | 0 | 1,160 | 1,160 |
| Desert Scrubs | 2,230 | 2,160 | 0 | 2,160 | 40 | 30 | 70 |
| Riversidean Alluvial Fan Sage Scrub | 5,770 | 2,850 | 1,380 | 4,230 | 190 | 1,350 | 1,540 |
| Coastal Sage Scrub | 145,620 | 44,040 | 32,210 | 76,250 | 25,970 | 43,400 | 69,370 |
| Peninsular Juniper Woodland and Scrub | 940 | 340 | 180 | 520 | 20 | 400 | 420 |
| Riparian Scrub, Woodland, Forest | 13,490 | 3,690 | 6,790 | 10,480 | 350 | 2,660 | 3,010 |
| Oak Woodlands and Forests | 15,180 | 2,000 | 6,880 | 8,880 | 4,140 | 2,160 | 6,300 |
| TOTAL | 486,130 | 85,370 (18%) |
82,220 (17%) |
167,590 (34%) |
49,310 (10%) |
269,230 (55%) |
318,540 (66%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
As described below under Data Characterization, 108 of the 240 recent point localities have a high location precision. Of these 108 point localities, 40 will be inside the Criteria Area or Public/Quasi-Public Lands. A total of 11 locations will be inside the Rural/Mountainous category. A total of 57 point localities will be outside of the MSHCP Conservation Area. Conservation of this species will be considered from a landscape perspective because the species has well defined habitat requirements and yet may use a wide variety of habitats for foraging and nesting. Additionally, there are Core Areas for focusing conservation efforts where the species is observed in large numbers in a clustered distribution.
In addition, there are definable locations composed of Core Areas for focusing conservation efforts which are included within the MSHCP Conservation Area. These conserved Core Areas include at least 8 of 12 breeding and foraging locations as follows: Prado Basin/Santa Ana River (9,670 acres), Lake Mathews-Estelle Mountain area (Existing Core C plus Proposed Extended Existing Core 2; 23,710 acres), Wasson Canyon (Subunit 5 of the Elsinore Area Plan; 2,320 acres), Temecula Creek (Subunit 2 of the Southwest Area Plan; 850 acres), Wilson Valley (Subunit 2 of the REMAP Area Plan; 33,540 acres), Quail Valley (Proposed Linkage 7; 3,400 acres), Lake Perris/Mystic Lake/San Jacinto Wildlife Area (Existing Core H; 17,470 acres), and Badlands (Proposed Core 3; 24,920 acres). A total of 113,150 acres of Core Areas (estimated by the subunit acreages or core and linkage acreage estimated where identified) are conserved within the MSHCP Conservation Area. In addition, the MSHCP Plan will maintain (once every 8 years) the continued use of, and successful reproduction within, 75 percent of the Core Areas. Successful reproduction is defined as a nest which fledged at least one known young.
Rural/Mountainous Designation
As depicted on the MSHCP Plan Map (Figure 3-1, MSHCP Volume I), certain areas adjacent to or in proximity to the MSHCP Conservation Area are designated as Rural/Mountainous in the County's General Plan. These areas are generally constrained for development due to steep topography and the level of development in these areas is anticipated to be of a low density, rural residential character. While these areas will not be included within the MSHCP Conservation Area or managed for the benefit of species conserved under the MSHCP, and the existing zoning/ordinances for these areas do not preclude development and could allow substantial fragmentation and/or degradation of habitat for proposed covered species, the low levels of development anticipated in these areas may provide a buffer to the MSHCP Conservation Area that may be of value to certain species. For the loggerhead shrike, conservation of the Santa Rosa Plateau and the Badlands is important for maintaining connectivity between the lowlands and San Diego County and between the lowlands and Cherry Valley/Banning, respectively. MSHCP Conservation Area locations in these areas are generally surrounded by Rural/Mountainous designations. Potential development in these areas is anticipated to retain vacant areas that will provide for movement for this species. Movement patterns of the shrike indicate that they disperse preferentially along connecting corridors of vegetation rather than between equally sized isolated patches of habitat (Haas 1995). The areas listed above include linkages which provide these connecting corridors of vegetation within the Rural/Mountainous designations. These linkages include Proposed Linkage 9, and Proposed Constrained Linkages 9 through 12 and 22 and 23. A total of 49,310 acres (10 percent) of habitat will be designated Rural/Mountainous.
MSHCP Conservation Area Configuration Issues
Several large blocks of habitat supporting the current known core populations with nesting and foraging locations, and potential foraging and nesting locations of the loggerhead shrike will be conserved as Criteria Area and Public/Quasi-Public lands including the Prado Basin/Santa Ana River (9,670 acres), the Interstate 15 corridor from El Cerrito to the San Diego County line including Lake Mathews-Estelle Mountain (Existing Core C plus Proposed Extension of Existing Core 2; 23,710 acres), Wasson Canyon (2,320 acres), Temecula Creek (850 acres), Quail Valley (Proposed Linkage 7; 3,400 acres), Wilson Valley (33,540 acres), Lake Perris/Mystic Lake/San Jacinto Wildlife Area (Existing Core H; 17,470 acres), and the Badlands (Proposed Core 3; 24,920 acres). Other locations of the species that will be conserved include those along the Interstate 15 corridor at Temescal Wash (4,010 acres), Alberhill (3,460 acres), Lake Elsinore grasslands and Collier Marsh (1,810 acres), Murrieta Creek (2,060 acres), and Sedco Hills (Proposed Linkage 8; 5,470 acres), also the Santa Rosa Plateau (Existing Core F plus Proposed Linkage 9; 11,460 acres), French Valley (Proposed Core 2; 5,050 acres), Lake Skinner/ Diamond Valley Lake area (Existing Core J plus Proposed Extended Existing Cores 5, 6, and 7, and Existing Constrained Linkage A; 29,370 acres), Upper San Jacinto River (Proposed Core 5; 3,220 acres), Lakeview Mountains (7,150 acres), Sycamore Canyon Regional Park (Existing Core D; 2,510 acres), Motte-Rimrock Reserve (Proposed Noncontiguous Habitat Block; 1150 acres), and San Timoteo Creek (2,290 acres). The acreage of each block listed above is based on the Subunit calculations unless identified as a specific core or linkage. As identified above, the species occurs within the MSHCP Plan Area as a nesting, foraging and wintering species, and as such, the MSHCP Conservation Area will provide adequate habitat for all phases of the life history including potential nest sites with adequate protection around each nest site, potential foraging areas, and contiguous habitat linkages between conserved areas, which have been reported as important for movements and dispersal of the loggerhead shrike.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 167,590 acres of suitable Conserved Habitat and 8 Core Areas which are composed of large blocks of habitat within the MSHCP Conservation Area. The Core Areas are provided with connections of Proposed or Existing Linkages or Constrained Linkages which connect the Proposed and Existing Cores. In addition, the MSHCP Plan will maintain (once every 8 years) the continued use of, and successful reproduction within, 75 percent of the Core Areas. Successful reproduction is defined as producing fledglings from a nesting attempt. The current population size of the loggerhead shrike is unknown, however a sizable data base is present within the UCR database and the species appears well represented throughout the MSHCP Plan Area except in the desert and high elevation areas. The literature documents the usage of desert areas, thus desert habitat has been included within the conservation analysis, however data point locations are likely lacking due to low survey effort in desert areas. Some concerns have been expressed regarding the impact the fire ant may have on the loggerhead shrike. Currently there is one known location of the fire ant. The area is currently under quarantine and efforts are being made to control and eradicate the ant. The location is outside the MSHCP Conservation Area and will have no effect on the conservation analysis of the loggerhead shrike.
INCIDENTAL TAKE
The Incidental Take of the loggerhead shrike is difficult to quantify due to our limited knowledge of its distribution and abundance within the Plan Area. The maximum level of Incidental Take of loggerhead shrike can be anticipated by the loss of the number of acres of habitat that will become unsuitable for this species. About 318,540 acres (66 percent) of habitat for the loggerhead shrike will be outside the Criteria Area and Public/Quasi -Public designations and individuals within these areas will be subject to Incidental Take consistent with the Plan. Four core population areas not included within the MSHCP Conservation Area include the Wildomar area, the area around San Jacinto except for a few small vernal pool preserve areas, Moreno Valley, and the scattered locations within the Homeland/Winchester/Menifee area.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The location database for the loggerhead shrike includes approximately 319 records dated from 1888 to 1999. Of the recent approximately 240 records, dated from 1990 to 1999, approximately 108 are high precision records and can be evaluated accurately for location. These high precision location records are located within various habitat types including sage scrub, cropland, non-native grassland, chaparral, riparian, woodlands, alluvial, dairy operations, alkali playa, orchard, and adjacent to reservoir, all of which are habitats in which the shrike could likely occur. Approximately 25 of the recent high precision records are located within residential land use and although this may indicate the record is no longer extant, it is also likely that the shrike was observed adjacent to residential development.
Although the loggerhead shrike is a passerine bird, it has a very raptorial natural history and life history strategy and is thus studied by ornithologists who are interested in small passerine birds as well as those scientists interested in the birds of prey. There is a moderate-to-large amount of literature available on this species including natural history studies, nesting and physiological ecology studies, and information on the management of the species. Little information is available specifically for the Plan Area other than the many recorded observations of this species.
Habitat and Habitat Associations
The loggerhead shrike is known to forage over open ground within areas of short vegetation, pastures with fence rows, old orchards, mowed roadsides, cemeteries, golf courses, riparian areas, open woodland, agricultural fields, desert washes, desert scrub, grassland, broken chaparral and beach with scattered shrubs (Unitt 1984; Yosef 1996). Individuals like to perch on posts, utility lines and often use the edges of denser habitats (Zeiner, et al. 1990). In some parts of its range, pasture lands have been shown to be a major habitat type for this species, especially during the winter season (Yosef 1996) and breeding pairs appear to settle near isolated trees or large shrubs (Yosef 1994). The highest density occurs in open-canopied valley foothill hardwood, valley foothill hardwood-conifer, valley foothill riparian, pinyon-juniper, juniper, desert riparian, and Joshua tree habitats; it occurs only rarely in heavily urbanized areas, but is often found in open cropland (Zeiner et al. 1990). In many regions, indices of the loggerhead shrike abundance correlate with the percentage of pastureland available (Gawlik and Bildstein 1993). In the Mojave Desert, the loggerhead shrike was observed more often in urban settings than other raptor species occurring there (Knight et al. 1999). In the midwest the habitat use of the shrike is defined as savannah habitat at the landscape scale but at the fine-scale, sites used by shrikes were characterized by tall, sparse, structurally heterogeneous herbaceous vegetation with high standing dead plant cover and low litter cover (Michaels and Cully 1998). The tree and shrub density did not differ between sites used and not used by shrikes (Michaels and Cully 1998).
Geographic Range
Throughout most of the southern portion of its range, the loggerhead shrike is a resident except as described by Terres (1980;Yosef 1996). The northern populations are migratory (Yosef 1996). The species nests from southern Canada through the Great Basin and California, to Baja California, Mexico and the Gulf coast (Terres 1980). Specifically, in western North America, the species breeds from southeastern Alberta, western Montana, northwest Wyoming, southern Idaho, south-central Washington, eastern Oregon, and California south to southern Baja California. In Central North America, it breeds from southern Saskatchewan and southwest Manitoba, North Dakota, and portions of southern Minnesota, eastern Iowa, northwest and southeast Missouri and northern Arkansas, south through Louisiana, Texas, New Mexico, and Arizona and through Mexico to north Sinaloa and Oaxaca. In eastern North America, it breeds in southern Wisconsin, and from southeast Illinois and southwest Ohio south to the Gulf Coast and from eastern West Virginia and all but the eastern portions of both Virginia and North Carolina south to the Gulf Coast and all but the extreme southern part of Florida (Yosef 1996).
Wintering grounds are found in the southern portion of the breeding range and further south into Mexico (Terres 1980). The northern populations are migratory and most winter from northern California, northern Nevada, northern Utah, central Colorado, southern and eastern Kansas, western Missouri, northern Kentucky, and northern Virginia south through the southern United States and in Mexico south throughout the breeding range (Yosef 1996).
It is difficult to document and compare historic and current distributions of the loggerhead shrike because the number of observers and level of survey effort has increased dramatically. Clearing of virgin forests and replacement by open farmlands may have allowed the species to become widely distributed before the beginning of the twentieth century. Many of the habitats in which this species breeds are seral stages of vegetation, although deserts, shrub steppes, and southern savannas may represent the historic Core Areas of its distribution (Yosef 1996).
In California, the species is found throughout the foothills and lowlands of California as a resident (Zeiner et al. 1990). Winter migrants are found coastally, north of Mendocino county (Zeiner et al. 1990). The loggerhead shrike seems to have always been most abundant in the southern and western portions of its range (Cade and Woods 1997).
Known Populations with Western Riverside County
The loggerhead shrike occurs throughout areas of suitable habitat as a yearlong resident, breeding and wintering in western Riverside County (Zeiner et al. 1990). The loggerhead shrike occurs relatively frequently within the central portion of the Plan Area with few records in the montane areas. It has a broad scattered distribution and some clustering of locations as described below.
Core areas occur along the Interstate 15 corridor and between Interstate 15 and 215 from the Prado Basin to Temecula, along the south central area to Aguanga, within the Badlands and in the Moreno Valley. Core areas include the Prado Basin/Santa Ana River, Lake Mathews-Estelle Mountain, Wasson Canyon, Wildomar, Temecula Creek, Wilson Valley, Quail Valley, San Jacinto, Lake Perris/Mystic Lake/San Jacinto Wildlife Area, Moreno Valley, Badlands, and scattered within the larger area of Homeland/Winchester/Menifee area. Other locations are scattered within the lowlands, foothills, and Santa Ana Mountains Bioregions including but not limited to Santa Rosa Plateau Nature Reserve, Cleveland National Forest, Aguanga, Beaumont, Alberhill, and Box Springs Mountains, however these locations do not contain clusters of recent and high precision data locations but may have one or more recent documented locations.
Biology
Genetics: The endangered San Clemente shrike, L. L. mearnsi, shows only 60 percent of the genetic variation of the mainland shrike population even though individuals of the subspecies gambeli visit the island annually; it has been concluded that the island population has evolved sufficient genetic independence to justify ongoing conservation efforts (Mundy et al. 1997a). Strong structure is apparent in the cytochrome b mtDNA sequence variations defining four haplotypes corresponding to the four subspecies (Mundy et al. 1997b). The similarity in haplotypes between populations from Saskatchewan and southern California suggests a post-glacial northern range expansion of the species (Mundy et al. 1997b).
Diet and Foraging: The loggerhead shrike foraging habitat includes open landscapes characterized by well-spaced, often spiny, shrubs and low trees, usually interspersed with short grasses, forbs, and bare ground, scrub lands, steppes, deserts, savannas, prairies, agricultural lands and some suburban areas (Yosef 1996). For foraging habitat, they appear to favor areas with fence lines and utility lines and poles for perching (Yosef 1996). In suboptimal foraging habitat areas, where grass is tall and dense, their foraging success is not affected, however their foraging methods are altered and include more hovering, more flights, and frequent changes in perches, generally more energetically expensive behaviors and thus larger prey items are taken (Yosef and Grubb 1993).
Individuals of the loggerhead shrike perch to search for prey which include large insects, small mammals, amphibians, reptiles, fish and invertebrates and they use impaling as a means of handling prey (Zeiner et al. 1990). Shrikes primarily subsist on large ground-dwelling insects and do not seem to require water (Miller and Stebbins 1964). Shrikes have been shown to be able to consume toxic insects by impaling and allowing them to "age" which apparently rids the then dead prey of the toxic chemical (Yosef and Whitman 1992).
Nestling shrikes have been successfully reared in captivity to create a model of feeding for the endangered San Clemente shrike. The artificially incubated, hatched and reared chicks were most successfully fed a varied diet consisting of mouse pups, egg and insects, which more closely resembles a diet provided in the wild than other artificial diets (Kuehler et al. 1993).
Daily Activity: The loggerhead shrike is a yearlong, diurnally active species (Zeiner et al. 1990). It spends approximately 80 percent of its day perched but will spend more time in flight in suboptimal foraging habitat areas (Yosef and Grubb 1993).
Reproduction: In an Idaho sagebrush (Artemisia tridentata) rangeland community, most loggerhead shrike nests (65 percent) were constructed in sage brush although bitterbrush and greasewood were also used frequently (Woods and Cade 1996). Nesting occurs in branches up to 4.5 meters above the ground frequently in a shrub with thorns or with tangled branching habits (Zeiner et al. 1990; Yosef 1996). Nests or nest materials are often reused in subsequent years (Yosef 1996). Height of nest shrubs average 162 centimeters and the mean height of nests was 79 centimeters although success of the nesting attempt did not appear to be related to the location of the nest but was more related to stochastic events such as predation and weather (Woods and Cade 1996). Porter et al. (1975) obtained reproduction data for a pair in shortgrass prairie habitat of Colorado. Mean nesting height was 2.03 meters, mean clutch size was 6.4 eggs, no double broods were observed although re-nesting was common if the nest failed (Porter et al. 1975). Throughout its range, the mean clutch size for the species is 5.4 eggs per nest with a range of 1 to 9 eggs (Yosef 1996). Loggerhead shrikes exhibit a latitudinal and longitudinal cline in clutch size with larger clutches at higher latitudes and farther west (Yosef 1996).
The parent shrikes may induce the young to fledge from the nest earlier than normal in order to avoid predation (Woods 1993). This may be due to the high predation rate on loggerhead shrike nestlings.
Loggerhead shrikes have been successfully hand-reared in captivity, will breed in captivity and can then be successfully released into the wild (Cade 1992).
Survival: The average nesting success of the loggerhead shrike, measured as the percent of nests in which at least one young fledges, is 56 percent (Yosef 1996). The large clutch size and relatively high rate of hatching success, potentially enables the loggerhead shrike to produce large numbers of offspring, although many young are lost through brood reduction and predation (Yosef 1996). Predation has been calculated to account for 52 percent of all nest failures and adverse weather accounts for 33 percent (Porter et al. 1975).
Dispersal: Juvenile dispersal of the loggerhead shrike has been measured at around 12 to 14.7 kilometers from the natal site with adults dispersing a mean distance of 2.7 kilometers (Yosef 1996; Collister and De Smet 1997). Movement patterns of the shrike indicate that they disperse preferentially along connecting corridors of vegetation rather than between equally sized isolated patches of habitat (Haas 1995).
Socio-Spatial Behavior: In those geographic locations where the species is a year-round resident, the loggerhead shrike usually lives in pairs on permanent territories (Yosef 1996). For populations that are migratory a territory is defended through the non-breeding season (Miller 1931; Smith 1973). Some pairs spend the entire year on a single territory and outside the breeding season, the mates may defend neighboring territories, which are coalesced at the beginning of the nesting season (Yosef 1996). Miller and Stebbins (1964) observed large territories of 12-16 hectares while Yosef (1996) sites a mean territory size of 8.5 hectares. Territories in California are jointly defended by pairs during the breeding season, but during the fall these pairs disband and defend separate, although often adjacent, winter territories (Yosef 1996).
Community Relationships: Loggerhead shrikes interact with many other avian species with which they share habitat; shrikes often dominate these interactions (Yosef 1996). Shrikes may also compete with the fire ant for food sources which may cause declines in the population of shrikes (Grisham 1994).
Threats to Species
Despite its wide distribution, the loggerhead shrike is one of the few North American passerines whose populations have declined continent-wide in the recent decades (Yosef 1996). Terres (1980) cites that shrike are often killed by automobiles early in the morning. In one study, the pesticide DDE may have reduced an Illinois population through eggshell thinning (Anderson and Duzan 1978; Morrison 1979). Pesticide use (organochlorines, DDE, etc.) may have potentially reduced eggshell thickness and altered development (Yosef 1996). Displacement of habitat through urban development, the spraying of biocides, and competition with species that are more tolerant of human-induced changes may be resulting in population declines (Yosef 1996). The loggerhead shrike is thought to be generally tolerant to human harassment, although it will abandon nesting attempts if disturbed (Yosef 1996). A study of the effect of spraying the common fertilizer, sodium ammonium nitrate, on cattle pastures concluded that the foraging territories of shrikes increased on average to 138 percent of a control group and the survivorship of eggs, nestlings and fledglings as well as adults was reduced, and one territory was abandoned (Yosef and Deyrup 1998).
The loggerhead shrike was once widely distributed and common over most of North America, occupying an exclusive breeding range with no other shrikes (Cade and Woods 1997). Although it occurs in a wide variety of plant associations, this shrike is generally found in landscapes characterized by widely spaced shrubs and low trees interspersed with short grasses, forbs, and bare ground, habitat conditions which are currently being developed (Cade and Woods 1997). Recently, Christmas bird count data and Breeding Bird Survey data have revealed an overall downward trend across the continent that appears to be related to alterations in habitat structure and loss of habitat as well as the loss of pasture lands and increase in intensive row-crop agriculture (Cade and Woods 1997; Prescott and Collister 1993; Telfer 1992; Gawlik and Bildstein 1993; Smith and Kruse 1992). Most populations along the coastal plains of southern California have been displaced by urban development, although the subspecies occupying the region (L. l. gambeli) is not yet in danger of extirpation (Morrison 1981).
The loggerhead shrike may suffer populations declines due to the presence of the fire ant. Studies have looked at changes in the shrike's winter habitat and found that, in addition to changes in land use, the shrike's decline in particular counties in the southern U.S. are directly correlated with an increase in fire ants in the area. The shrike and fire ant are direct competitors for food sources. Both feed on invertebrates, reptiles, and small mammals. It is possible that fire ant control could benefit the loggerhead shrike in those areas where they co-occur (Grisham 1994). Within western Riverside County, there is currently one location of the fire ant: Morena Valley, north of Interstate 60 and east of Pigeon Pass Road.
The San Clemente loggerhead shrike appears to be threatened by the introduction of exotic species which have altered the ecosystem of San Clemente Island including loss of suitable habitat and increased predation of nests and adults (Scott and Morrison 1990).
Special Biological Considerations
Smyth and Coulombe (1971) report that the loggerhead shrike does not drink water up to ambient air temperatures of 40°C. The loggerhead shrike has a basal metabolic rate that is lower than predicted for a passerine its size but that is more similar to other raptor species (Cunningham 1979). Additionally, it has an extended thermoneutral zone from approximately 24 to over 36 degrees C (Weathers, et al. 1984). Cunningham (1979) concluded that as an animal that is a sit and wait predator, it benefits from having a reduced basal metabolic rate. The most metabolically expensive behavior of the bird is flight (Weathers, et al. 1984) which it uses rarely: it spends approximately 80 percent of its day perched but will spend more time in flight in suboptimal foraging habitat areas (Yosef and Grubb 1993). Management implications are that short grass areas are important to include for use by shrikes for hunting (Yosef and Grubb 1993).
In addition to using barbed wire for impaling food items, the loggerhead shrike has been observed using barbed wire to anchor and tear nest-lining materials (Burton 1999). Effects of protective fencing were found to result in higher abundance and species richness of birds, including the loggerhead shrike for which nesting was also found to be more frequent inside the fenced area. This increase in abundance may be related to an increase in abundance of seed and invertebrate food sources, and particularly for the shrike, an increase in reptile prey species (Brooks 1999).
Sites used by loggerhead shrikes did not differ with respect to military training disturbance, hay harvest, or the number of years since a site was last burned (Michaels and Cully 1998). Movement patterns of the shrike concluded that they disperse preferentially along connecting corridors of vegetation than between equally sized isolated patches of habitat (Haas 1995). Management for resident shrikes should include a patchwork of grassy habitats and sparsely vegetated bare areas at the scale of individual shrike territories (Gawlik and Bildstein 1993). Similarly, in southern Alberta, comparisons of occupied and unoccupied sites indicate that the availability of suitable habitat for breeding could be increased by management practices that increase the prevalence of grasslands (Prescott and Collister 1993; Telfer 1992). Woods and Cade (1996) found shrublands to be a very important habitat used by the shrike for nesting and that a contraction in both range and numbers of shrikes has occurred as the appropriate habitat has been lost.
Brooks and Temple (1990) used a model to demonstrate that a minimum of 5.5 fledglings per breeding pair per season was required for a stable population in Minnesota if the territory reoccupancy of 47 percent equals the adult survival and assuming that first year survival of 19 percent is correct. This appears to be an unrealistic model and the investigators found a rate of only 2.07 fledgings per breeding pair per season.
Since reproductive rates are potentially high in this species, it could expand its current numbers and range if the factors responsible for its recent decline can be identified and eliminated. In some studies, the reproductive success of loggerhead shrikes is relatively high and does not explain the recent decline in shrike populations (Gawlik and Bildstein 1990). Although much good habitat has been lost, enough remains unoccupied to accommodate a larger population (Yosef 1996). Management initiatives aimed at benefitting the loggerhead shrike should be directed toward increasing prevalence of medium and perhaps tall grass in favorable areas for populations. This can be achieved by controlling grazing and mowing of grasslands. It is also desirable to maintain brush along fence lines, scattered trees in pastures and fields and hedges as potential nest sites (Yosef 1996). The density of hunting perches affects the nutritional condition of shrikes (Yosef and Grubb 1992). Areas devoid of shrike territories have been noted to contain few fences and sparse trees, thus these areas may have been subthreshold economically because of insufficient foraging features for shrikes. The continuing declines of the loggerhead shrike may be at least partially due to withdrawal from parts of the species range in which man's activities have reduced the density of hunting perches (Yosef and Grubb 1992).
Key management priorities for the loggerhead shrike include: determine the migration routes, stopover and wintering areas and the susceptibility to human disturbance at these locations; evaluate the dietary needs and how weather, season, land use, and biocides influence food availability; determine the mortality rates of fledged juveniles and adults throughout the annual cycle in different habitats; determine the degree of niche overlap between the loggerhead shrike and potential competitors to see whether shrike productivity is correlated with the presence or absence of these species (Yosef 1996).
LITERATURE CITED
Anderson, W. L. and R. E. Duzan. 1978. DDE residues and eggshell thinning in loggerhead shrikes. Wilson Bulletin 90:215-220.
Bartholomew, G. A. and T. J. Cade. 1963. The water economy of land birds. Auk 80:504-539.
Brooks, M. 1999. Effects of protective fencing on birds, lizards, and black-tailed hares in the western Mojave Desert. Environmental management 23: 387-400.
Brooks, M. and S. A. Temple. 1990. Habitat availability and suitability for loggerhead shrikes in the upper midwest. Am. Midl. Nat. 123: 75-83.
Burton, K. M. 1999. Use of barbed wire by loggerhead shrikes (Lanius ludovicianus) to manipulate nest materials. American Midland Naturalist 142: 198-199.
Cade, T. J. 1992. Hand-reared loggerhead shrikes breed in captivity. Condor 94: 1027-1029.
Cade, T. J. and C. P. Woods. 1997. Changes in distribution and abundance of the loggerhead shrike. Conservation Biology 11: 21-31.
Collister, D. M and K. De Smet. 1997. Breeding and natal dispersal in the loggerhead shrike. J. Field Ornithology 68: 273-282.
Cunningham, K. G. 1979. Bioenergetics of the loggerhead shrike relation between lifestyle and metabolism. Master's thesis. University of California, Irvine.
Garrett, K. and J. Dunn. 1981. Birds of southern California. Los Angeles Audubon Society 408pp.
Gawlik, D. E. And K.L. Bildstein.. 1990. Reproductive success and nesting habitat of loggerhead shrikes in north-central South Carolina. Wilson Bull. 102: 37-48.
Gawlik, D. E. And K.L. Bildstein. 1993. Seasonal habitat use and abundance of loggerhead shrikes in South Carolina, USA. J. Wildlife Management 57: 352-357.
Grisham, J. 1994. Attack of the fire ant. BioScience 44: 587-590.
Haas, C. M. 1995. Dispersal and use of corridors by birds in wooded patches on an agricultural landscape. Conservation Biology 9: 845-885.
Knight, R. L., R. J. Camp, W. I. Boarman, H. A. L. Knight. 1999. Predatory bird populations in the east Mojave Desert, California. Great Basin naturalist 59: 331-338.
Keuhler, C. M., A. Lieberman, B. McIlraith, W. Everett, T. A. Scott, M.L. Morrison, and C. Winchell. 1993. Artificial incubation and hand-rearing of loggerhead shrikes. Wildlife Society Bulletin 21: 165-171.
Michaels, H. L. and J. F. Cully. 1998. Landscape and fine scale habitat associations of the loggerhead shrike. Wilson Bulletin 110: 474-482.
Miller, A. H. 1931. Systematic revision and natural history of the American shrikes (Lanius). University of California Publications in Zoology 38:11-242.
Miller, A. H. and R. C. Stebbins. 1964. The lives of desert animals in Joshua Tree National Monument. University of California Press, Berkeley. 452pp.
Morrison, M. L. 1979. Loggerhead shrike eggshell thickness in California and Florida. Wilson Bulletin 91:468-469.
Morrison, M. L. 1981. Population trends of the loggerhead shrike in the United States. American birds 35: 754-757.
Mundy, N. I., C. S. Winchell, T. Burr, and D. S. Woodruff. 1997a. Microsatellite variation and microevolution in the critically endangered San Clemente Island loggerhead shrike (Lanius ludovicianus mearnsi). Proc. Royal Society of London, Series B, Biological Sciences 264: 869-875.
Mundy, N. I., C. S. Winchell, and D. S. Woodruff. 1997b. Genetic differences between the endangered San Clemente Island loggerhead shrike Lanius ludovicianus mearnsi and two neighboring subspecies demonstrated by mtDNA control region and cytochrome b sequence variation. Molecular Ecology 6: 29-37.
Porter, D. K., M. A. Strong, J. B. Giezentanner, and R. A. Ryder. 1975. Nest ecology, productivity, and growth of the loggerhead shrike on the shrotgrass prairie. Southwestern Naturalist 19:429-436.
Prescott, D. R. And D. M. Collister. 1993. Characteristics of occupied and unoccupied loggerhead shrike territories in southern Alberta. J. Wildlife Management 57: 346-352.
Reynolds, T. D. 1979. The impact of loggerhead shrikes on nesting birds in a sagebrush environment. Auk 96:798-800.
Scott, T. A. And M. L. Morrison. 1990. Natural history and management of the San Clemente loggerhead shrike. Proc. Western Foundation of Vertebrate Zoology 4: 23-57.
Smith, S. M. 1973. Aggressive display and related behavior in the loggerhead shrike. Auk 90:287-298.
Smith, E. L. And K. C. Kruse. 1992. The relationship between land-use and the distribution and abundance of loggerhead shrikes in south-central Illinois. J. Field Ornithology 63: 420-427.
Smyth, M. and H. N. Coulombe. 1971. Notes on the use of desert springs by birds in California. Condor 73:240-243.
Telfer, E. S. 1992. Habitat change as a factor in the decline of the western Canadian loggerhead shrike Lanius ludovicianus population. Canadian field-Naturalist 106: 321-326.
Terres, J. K. 1980. The Audubon Society Encyclopedia of North American Birds. Alfred A. Knopf, New York, New York. 1109pp.
Unitt, P. 1984. The birds of San Diego County. San Diego Society of Natural History: Memoir 13, San Diego, California. 276pp.
Weathers, W. W., W. A. Buttemer, A. M. Hayworth, and K. A. Nagy. 1984. An evaluation of time-budget estimates of daily energy expenditure in birds. Auk 101: 459-472.
Woods, C. P. 1993. Parent loggerhead shrikes induce nestling to fledge. Wilson Bulletin 105: 532-433.
Woods, C. P. And T. J. Cade. 1996. Nesting habits of the loggerhead shrike in sagebrush. Condor 98: 75-81.
Yosef, R. 1994. The effects of fence lines on the reproductive success of loggerhead shrikes. Conservation Biology 8: 281-285.
Yosef, R.. 1996. Loggerhead shrike (Lanius ludovicianus). In The Birds of North America, No. 231 (A. Poole and F. Gill, eds.). The Academy of Natural Sciences, Philadelphia, and The American Ornithologists' Union, Washington, D.C.
Yosef, R., and T. C. Grubb. 1993. Territory size influences nutritional condition in non-breeding loggerhead shrikes (Lanius ludovicianus): a ptilochronology approach.
Yosef, R., and T. C. Grubb. 1993. Effect of vegetation height on hunting behavior and diet of loggerhead shrikes. Condor 95: 127-131.
Yosef, R., and M. A. Deyrup. 1998. Effects of fertilizer-induced reduction of invertebrates on reproductive success of loggerhead shrikes (Lanius ludovicianus). J. Fuer Ornithologie 139: 307-312.
Yosef, R. And D. W. Whitman. 1992. Predator adaptations and defensive adaptations in evolutionary balance : no defense is perfect. Evolutionary Ecology 6: 527-536.
Zeiner, D.C., W. F. Laudenslayer, K. E. Mayer and M. White eds. 1990. California's Wildlife: Volume II - Birds. California Department of Fish and Game. Sacramento, California. 732 pp.
MacGillivray's warbler (Oporornis tolmiei)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
MacGillivray's warbler (Oporornis tolmiei)
Status:
State: None
Federal: None
GROUP DESIGNATION AND RATIONALE
Group 1
The MacGillivray's warbler has a sparse and widespread distribution throughout the MSHCP Plan Area within a variety of shrubby and riparian habitats. It occurs within the lowland and foothill Bioregions of the Plan Area as a transient in the spring and fall but does not winter within these Bioregions. It has been documented within the literature as occurring commonly within the lowland and foothills area as a transient that may use densely vegetated shrub and scrub habitats. However, there are few documented records of the species, probably because it is relatively common and observations may not be recorded. It breeds within the Plan Area within the mountain Bioregions in scrub and forested habitats. Although it has few documented records, the literature documents its occurrence within the mountain regions of the Plan Area and that the populations have increased significantly within the mountain regions of the Plan Area.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 418,780 acres of riparian scrub, forest, and woodland, oak woodland and forest, montane coniferous forest, coastal sage scrub, chaparral, Riversidean alluvial fan sage scrub, and desert scrub habitats for breeding, dispersal, and transient movements. The breeding and transient movement areas have been combined in this analysis because this species uses the same habitats for both parts of the life cycle and there may be some overlap between breeding areas and migration areas.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
For the purpose of the conservation analysis, potential breeding and transient movement habitat for the MacGillivray's warbler includes montane coniferous forest and woodland, riparian scrub, woodland, and forest habitat, oak woodland and forest, chaparral, coastal sage scrub, desert scrub, and Riversidean alluvial fan sage scrub. Based on these habitats, the Plan Area supports approximately 659,350 acres of potential habitat for the MacGillivray's warbler. Table 1 shows the conservation and loss of potential habitat for the MacGillivray's warbler. Overall, approximately 418,780 acres (64 percent) of potential habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public Lands.
This species occurs within Forest Service lands for nesting within montane coniferous woodland, riparian scrub, forest, and woodland, oak woodland and forest, chaparral, coastal sage scrub, and Riversidean alluvial fan sage scrub. Under the existing Forest Land allocation plan, these locations or habitats generally are located within the San Jacinto wilderness areas as well as in most of the grazing allotments. Timber harvest has a potential to directly affect the breeding habitat and breeding activity of the MacGillivray's warbler. The Forest Service may reduce the potential for this by identifying important breeding areas and maintaining them in suitable breeding habitat condition.
As described below under Data Characterization, 9 of the 13 relatively recent point localities have high precision. Of these 9 point localities, 1 will be inside the Criteria Area and 1 is located within Public/Quasi-Public Lands. Of the 7 high precision recent points located outside the MSHCP Conservation Area, all are located in lowland bioregion residential/urban/exotic or agriculture areas and were observed during migration. The data point locations are highly under-represented due to lack of reporting or surveys. MacGillivray's warbler is observed frequently especially during migration but has also been documented in the national forest areas (Hayworth, 1990, pers. obs.). Providing additional suitable habitat that is not currently occupied may assist with the conservation of the species.
TABLE 1
SUMMARY OF HABITAT CONSERVATION FOR
MACGILLIVRAY'S WARBLER
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| Chaparral | 413,470 | 64,900 | 207,370 | 272,270 | 59,580 | 81,620 | 141,200 |
| Coastal Sage Scrub | 152,690 | 47,160 | 34,560 | 81,720 | 26,240 | 44,730 | 70,970 |
| Desert Scrubs | 9,360 | 3,670 | 1,310 | 4,980 | 40 | 4,340 | 4,380 |
| Montane Coniferous Forest | 29,890 | 20 | 20,480 | 20,500 | 40 | 9,350 | 9,390 |
| Riparian Scrub, Woodland, Forest | 14,610 | 3,920 | 7,270 | 11,190 | 370 | 3,050 | 3,420 |
| Riversidean Alluvial Fan Sage Scrub | 7,150 | 3,170 | 2,060 | 5,230 | 220 | 1,700 | 1,920 |
| Woodlands and Forests (oak) | 32,180 | 2,390 | 20,500 | 22,890 | 5,020 | 4,270 | 9,290 |
| TOTAL | 659,350 | 125,230 (19%) | 293,550 (45%) |
418,780 (64%) |
91,510 (14%) |
149,060 (23%) |
240,570 (36%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
In addition to the above protection, the Riparian/Riverine Areas and Vernal Pools policy described in Section 6.1.2 provides for conservation of wetlands which provide foraging and breeding habitat for this species through avoidance and minimization. Mitigation for impacts to wetlands shall be incorporated in accordance with the "No Net Loss" policy of federal and state wetland regulations. This policy may provide some protection for foraging habitat of the MacGillivray's warbler in the riparian scrub and woodland areas.
MSHCP Conservation Area Configuration Issues
Several large blocks of habitat supporting or potentially supporting the MacGillivray's warbler will be conserved as Criteria Area and Public/Quasi-Public designations, including the breeding habitat within the San Bernardino Mountains and the San Jacinto Mountains and potential or known transient movement or migratory stopover areas at the Prado Basin, Santa Ana River, Temescal Wash, Lake Mathews-Estelle Mountain, Wasson Canyon, Sedco Hills, Santa Rosa Plateau, Vail Lake/Wilson Valley, Temecula, Murrieta, and Tucalota creeks, Lake Skinner-Diamond Valley Lake, Mystic Lake/San Jacinto Wildlife Area, Lake Perris, Sycamore Canyon Regional Park, Box Springs, and Badlands. Protection is also provided within the San Bernardino National Forest roadless areas and wilderness areas. Some of the large blocks of potential habitat have not been mapped as containing MacGillivray's warblers either due to lack of surveys or lack of reporting observations. However, these habitat blocks have potential foraging habitat and within the higher elevations contain potential breeding habitat and could be occupied by MacGillivray's warblers in the future. As a long-distance migrant, MacGillivray's warblers are likely able to discover and use patches of habitat that have not been documented to be used in the past. As such, the MSHCP Conservation Area will provide adequate blocks of a variety of densely vegetated upland and riparian habitat as Core Areas for this species and will provide large patches of higher elevation habitat composed of conifer woodlands.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 418,780 acres of suitable Conserved Habitat including riparian scrub, forest, and woodland, oak woodland and forest, montane coniferous forest, coastal sage scrub, chaparral, Riversidean alluvial fan sage scrub, and desert scrub habitats for breeding, dispersal, and transient movements. The MSHCP Conservation Area has been designed to preserve the large blocks of areas that contain a variety of potentially suitable habitat for foraging use during migration as well as very large blocks that contain potentially suitable nesting habitat for the species.
INCIDENTAL TAKE
About 240,570 acres (36 percent) of potential habitat for the MacGillivray's warbler will be outside the Criteria Area or Public/Quasi-Public designations, and individuals within these areas will be subject to Incidental Take consistent with the Plan.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The location database for the MacGillivray's warbler includes 19 records from 1900 to 1999. Of the 13 recent records, dated from 1990 to present, nine records have a high precision level. These high precision records are located within sage scrub, riparian, chaparral, grassland, cropland, and developed habitats and likely reflect migratory birds due to the location within lowland areas that are not used for breeding. There are no recent records within mountain Bioregions which could represent a breeding location. This is either due to lack of survey effort or lack of reporting observations of the species.
A low-to-moderate amount of literature is available for the MacGillivray's warbler, mostly relating to general natural history and warblers in general. Few controlled scientific studies have been conducted and little management information is available. Very little information is available for the Plan Area other than what is available regarding basic distribution information.
Habitat and Habitat Associations
Breeding pairs of MacGillivray's warbler typically are found in moist brushy areas within coniferous forests between 2,000-2,800 meters but may also be found in clear-cuts or mixed deciduous forests up to 3,000 meters (Pitocchelli 1995; Garrett and Dunn 1981). The species prefers secondary-growth woodlands, brushy areas near water and dense willow canyon drainages (Terres 1980). It requires dense undergrowth and moderate cover with the amount of cover being important for assessing breeding habitat in coniferous and deciduous forest. It breeds in deciduous forests with 60 percent total cover, composed of 44 percent shrubs 8 percent coniferous species, 7 percent deciduous species (Morrison 1981).
Throughout California MacGillivray's warbler inhabits Valley foothill riparian, coastal Douglas-fir, redwood, montane riparian and desert riparian habitats (Zeiner et al. 1990). It has been characterized as breeding commonly in riparian habitat and clearcuts of northern coniferous forests, second growth, and disturbed habitat. It occurs in moist habitats, willow thickets, brushy areas, usually near water, from sea level along the Pacific Northwest coast to 3,000 meters in the Sierra Nevada range. In California, it prefers the upper Sonoran and Canadian life zones, and is possibly also present in the eastern Mohave Desert region.
In migration MacGillivray's warblers are elusive, mostly seen passing through thick shrubbery, but avoiding trees (Pitocchelli 1995, Miller and Stebbins 1964). It is common in dense shrubs or well-shaded habitats along mountains and desert of interior California. It may be observed in several different habitats in Utah during migration. Within San Diego county the species is known from weedy brush, streamside thickets and desert wash scrub (Unitt 1984).
Biogeography
The birds nest from southern Alaska, south to central California to central New Mexico (Terres 1980). Specifically, within suitable habitat, the species occurs along the Rocky Mountains, west to the Pacific Ocean, from southeast Alaska, to British Columbia, the Yukon, south to northern New Mexico, central Arizona, and southern California within the San Bernardino Mountains (Pitocchelli 1995). Within California, breeding populations occur in coastal areas, north of Monterey county and in the Sierras (Zeiner, et al. 1990). The populations tend to be more disjunct at the periphery of the breeding range, especially within the prairies and in the southwestern United States (Pitocchelli 1995).
The species winters in southern Baja California, Mexico to Panama but this is poorly defined (Terres 1980). It is a highly migratory species however little is known about the nature of migration because of the species preference for dense undergrowth and its elusive and shy behavior. The earliest spring migrants appear in March in California and pass through the lowland areas into late May (Pitocchelli 1995).
The current breeding range may be much smaller than the ancestral range. It has been speculated that the breeding range of the ancestor of the mourning and MacGillivray's warblers may have stretched across North America prior to the Pleistocene. Subsequent glaciation during the Pleistocene divided the range into the eastern and western populations. Overall, the MacGillivray's warbler populations have expanded since the late 1880s in the western United States. The MacGillivray's warbler shows an expanding range in parts of southern California especially in the San Gabriel and San Bernardino mountains (Pitocchelli 1995).
Known Populations with Western Riverside County
In southern California, MacGillivray's warbler is more common in the interior than coastal regions with known populations in the San Bernardino and San Gabriel mountains (Zeiner, et al. 1990). During migration, the species may occur throughout the western Riverside County region as a spring and fall transient through the central portion of the Plan Area (Garrett and Dunn 1981).
The species has been recorded sparsely in several locations: in the San Bernardino National Forest, probably as a breeding bird, and at other lowland locations as a migrant during either spring or fall, including Wasson Canyon, Sycamore Canyon Wilderness Park, Lake Mathews, Santa Ana River, Box Springs Mountains, Mystic Lake/San Jacinto Wildlife Area, Motte-Rimrock Reserve, Murrieta, Murrieta Hot Springs, and Santa Rosa Plateau east and west.
Biology
Genetics: The mourning and MacGillivray's warblers have been studied to determine their closeness of taxonomy and have been found to be distinct species. The mourning warbler is larger based on skeletal characters and has a lower song frequency. There is no hybrid contact zone (Pitocchelli 1990).
Diet and Foraging: MacGillivray's warbler eats mostly insects, including true bugs, leaf hoppers, beetles, bees, wasps and ants, foraging from shrubs or the ground in dense thickets (Zeiner, et al. 1990). It forages by gleaning along the inner parts of the vegetation at a height ranging from ground level to 3 meters (Pitocchelli 1995).
Daily Activity: The MacGillivray's warbler is a year-long diurnally active species (Zeiner, et al. 1990). It is not known if it migrates at night or during the day.
Reproduction: MacGillivray's warbler typically nests in riparian habitat along stream and river banks within the undergrowth of deciduous and mixed forests, logging clear cuts and areas recovering from avalanches. It may nest on clumps of grass on or above ground among cedar, alder, hawthorn, willows, flowering shrubs of wild raspberry, stinging nettle, buckthorn, saskatoon, wild rosebush, gooseberry, currant, blackberry vines, huckleberry, wild lettuce, heliobore, salal bush, hazel bush, wild columbine, dry ferns and wildflowers. The nest is always by shrubs and dense undergrowth (Pitocchelli 1995). Nesting occurs in shrubs in moist thickets from May through July with peak activity in June, laying 3-6 eggs, usually 4 eggs (Zeiner, et al. 1990; Pitocchelli 1995). Incubation is 11-13 days by the female only and the altricial nestlings are tended by both parents until fledging occurs (Zeiner, et al. 1990).
Survival: The estimated maximum age of an adult male MacGillivray's warbler in Oregon was 4 years 1 month (Klimkiewicz and Futcher 1989).
Dispersal: Family groups of MacGillivray's warbler appear to forage together during the post-fledging period but it is not known how long they stay together (Pitocchelli 1995). Based on the survival study cited above, the MacGillivray's warbler appears to have some site fidelity although the degree to which it operates is unknown.
Socio-Spatial Behavior: Species density of the MacGillivray's warbler has been recorded at 10 and 2.5 pairs per 100 acres for two study groups in Idaho (Johnston 1949). A separate study found a density of 10 per 100 acres in willow-sedge swamp, 30 per 100 acres in a flat land aspen stand and 85 per 100 acres in a scrub-meadow in Wyoming (Salt 1957).
Community Relationships: MacGillivray's warbler is preyed upon by accipiters, small mammals and snakes (Zeiner, et al. 1990).
Threats to Species
Parasitism of MacGillivray's warbler by cowbirds occurs rarely and is thought to not be a significant problem for the species (Bent 1953; Zeiner, et al. 1990).
MacGillivray's warbler is susceptible to pesticide contamination (acephate) resulting in depressed cholinesterase (ChE) activity (Pitocchelli 1995). Exposure to two other insecticides, however (carbaryl and trichlorfon), resulted in minor effects on the ChE activity, thus the influence of pesticides on the populations is undetermined (Pitocchelli 1995).
Ranching activities destroy the habitat of MacGillivray's warbler at migratory stopovers and on the wintering and breeding grounds, however, some human activities, such as logging, may benefit the species as described below (Pitocchelli 1995).
The MacGillivray's warbler responds differently to different types of human development. Extensive logging in the Pacific Northwest apparently is a benefit to this species (Pitocchelli 1995). However, a different study that included comparative studies of logged versus unlogged conifer forests concluded that the MacGillivray's warbler responds negatively to the logging activity (Medin 1985). This conclusion, in contradiction to the conclusion by Pitocchelli (1995), may be due to the different methods of logging. The logged forests that showed declines in the MacGillivray's warbler populations were cut commercially to a 10-inch minimum diameter in three separate and well-spaced cutting units. When studies were conducted on selection-cut logging forests, which harvest certain species but leave a variety of sizes, the MacGillivray's warbler showed an upward pattern of numerical response in population size (Medin and Booth 1989).
Special Biological Considerations
The MacGillivray's warbler is a relatively secretive bird outside of the breeding season, and is frequently detected only by the call note that it emits while foraging or perching within dense shrubs. During the breeding season within the montane areas, the male may perch at a high location to sing but otherwise remains relatively secretive (Beedy and Granholm 1985).
Breeding Bird Surveys show highest densities of this species in British Columbia and Washington but population trends within different regions of the United States are contradictory with some investigators reporting increases and others reporting long-term declines. Overall, within the Plan Area, it has been concluded that MacGillivray's warbler is increasing in population size (Pitochelli 1995).
Maintenance of riparian vegetation in and around montane meadows may be important for this species. Surface water diversion, groundwater extraction, heavy recreation use, facilities development, and overgrazing by livestock can degrade the montane riparian habitat (Stephenson and Calcarone 1999).
LITERATURE CITED
Bent, A. C. 1953. Life histories of North American wood warblers. U.S. National Museum Bulletin 203. 734pp.
Beedy, C. E. And S. L. Granholm. 1985. Discovering Sierra Birds. Yosemite national history Association and Sequoia Natural History Association. 229 pp.
Garrett, K. and J. Dunn. 1981. Birds of southern California. Los Angeles Audubon Society. 408pp.
Hayworth,A. 1990. Pers. obs., Advanced Sciences, Inc.
Klimkiewicz, M. K., and A. G. Futcher. 1989. Longevity records of North American birds supplement. J. Field Ornithol. 60: 469-494.
Johnston, D. W. 1949. Populations and distribution of summer birds of Latah County, Idaho. Condor 51:140-149.
Medin, D. E. 1985. Breeding bird responses to diameter-cut logging in west-central Idaho. United States Department of Agriculture, Forest Service, Intermountain Research Station. Research Paper INT-355.
Medin, D. E., and G. D. Booth. 1989. Responses of birds and small mammals to single-tree selection logging in Idaho. U.S.D.A. Forest Service, Intermountain Research Station. Research Paper INT-408.
Miller, A. H. and R. C. Stebbins. 1964. The lives of desert animals in Joshua Tree National Monument. University of California Press, Berkeley. 452pp.
Morrison, M. L. 1981. The structure of western warbler assemblages: analysis of foraging behavior and habitat selection in Oregon. Auk 98: 578-588.
Pitocchelli, J. 1995. MacGillivray's warbler (Oporonis tolmiei). In The Birds of North America, No. 158 (A. Poole and F. Gill, eds.). The Academy of Natural Sciences, Philadelphia, and The American Ornithologists' Union, Washington, D.C.
Pitocchelli, J. 1990. Plumage, morphometric, and song variation in mourning (Oporornis philadelphia) and MacGillivray's (Oporornis tolmiei) warblers. Auk 107: 161-171.
Salt, G. W. 1957. An analysis of avifaunas in the Teton Mountains and Jackson Hole, Wyoming. Condor 59:373-393.
Stephenson, J. R. and G. M. Calcarone. 1999. Southern California mountains and foothills assessment: habitat and species conservation issues. General Technical Report GTR-PSW-172. Albany, CA: Pacific Southwest Research Station, Forest Service, U.S. Department of Agriculture. 402 pp.
Terres, J. K. 1980. The Audubon Society Encyclopedia of North American Birds. Alfred A. Knopf, New York, New York. 1109pp.
Unitt, P. 1984. The birds of San Diego County. San Diego Society of Natural History: Memoir 13, San Diego, California. 276pp.
Zeiner, D.C., W. F. Laudenslayer, K. E. Mayer and M. White eds. 1990. California's Wildlife: Volume II - Birds. California Department of Fish and Game. Sacramento, California. 732pp.
merlin (Falco columbarius)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
merlin (Falco columbarius)
Status:
State: Species of Special Concern
Federal: None
GROUP DESIGNATION AND RATIONALE
Group 1
The merlin has a sparse and widespread distribution throughout the MSHCP Plan Area within almost every habitat that occurs within the Plan Area. It occurs within the Plan Area as a transient in the spring and fall and may occasionally winter within the area. It does not require specific conditions or locations for nesting because it does not nest in the region. It is an opportunistic predator that may forage anywhere in the area.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 193,840 acres of agriculture (field crops), grassland, freshwater marsh, cismontane alkali marsh, playa and vernal pool, desert scrubs, Riversidean alluvial fan sage scrub, coastal sage scrub, peninsular juniper woodland and scrub, riparian scrub, woodland and forest, and oak woodlands and forest habitats.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
The merlin uses sparse trees, open woodland, and riparian habitat for roosting and possibly foraging and a wide variety of more open habitats, including grasslands, shrub and scrub habitats for foraging (Garrett and Dunn 1981). Because they will opportunistically use a relatively wide variety of habitats for foraging, a wide range of habitats has been included for this analysis. For the purpose of the conservation analysis, potential habitat for the merlin includes agriculture (field crops), grassland, freshwater marsh, cismontane alkali marsh, playa and vernal pool, desert scrubs, Riversidean alluvial fan sage scrub, coastal sage scrub, peninsular juniper woodland and scrub, riparian scrub, woodland and forest, and oak woodlands and forest. Their roosting and perhaps foraging habitat is composed of habitat with sparse trees such as riparian, and deciduous woodland or forest and the Peninsular juniper woodland and scrub. The merlin will essentially use any available habitat except for dense coniferous woodland and open water. Based on these habitats, the Plan Area supports approximately 496,270 acres of potential habitat for the merlin. Table 1 shows the conservation and loss of potential habitat for the merlin. Overall, approximately 193,840 (39 percent) of potential habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public Lands. Management actions will be incorporated into the conservation strategy so that suitable habitat conditions will be maintained.
As described below under Data Characterization, 15 of the 24 recent point localities have a high location precision of "1." Of these 15 point localities, 6 will be inside the Criteria Area or Public/Quasi-Public lands and 2 will be inside the Rural/Mountainous category. A total of 7 point localities will be outside of the MSHCP Conservation Area. None of the major areas, Prado Basin, Santa Ana River, Mystic Lake/San Jacinto Wildlife Area, Lake Skinner/Diamond Valley Lake area, Wilson Valley, and Lake Mathews-Estelle Mountain, where the merlin has been observed in the past are outside the MSHCP Conservation Area. Conservation of this species should be considered from a landscape perspective because the species is found throughout the Plan Area and may occur in a variety of habitats. While there are definable locations for focusing conservation efforts, there do not appear to be Core Areas that will be essential for conservation of the species.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
MERLIN
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| All Bioregions | |||||||
| Agriculture (field crops) | 123,780 | 7,250 | 9,940 | 17,190 | 820 | 105,770 | 106,590 |
| Grassland | 146,870 | 20,010 | 22,810 | 42,820 | 12,220 | 91,830 | 104,050 |
| Cismontane Alkali Marsh | 150 | 40 | 0 | 40 | 0 | 110 | 110 |
| Freshwater Marsh | 470 | 170 | 240 | 410 | 0 | 60 | 60 |
| Playas and Vernal Pools | 7,910 | 3,830 | 2,920 | 6,750 | 0 | 1,160 | 1,160 |
| Desert Scrubs | 9,380 | 3,680 | 1,310 | 4,990 | 40 | 4,350 | 4,390 |
| Riversidean Alluvial Fan Sage Scrub | 7,150 | 3,170 | 2,060 | 5,230 | 220 | 1,700 | 1,920 |
| Coastal Sage Scrub | 152,690 | 47,160 | 34,560 | 81,720 | 26,240 | 44,730 | 70,970 |
| Peninsular Juniper Woodland and Scrub | 1,080 | 340 | 270 | 610 | 20 | 450 | 470 |
| Riparian Scrub, Woodland, Forest | 14,610 | 3,920 | 7,270 | 11,190 | 370 | 3,050 | 3,420 |
| Oak Woodlands and Forests (oak) | 32,180 | 2,390 | 20,500 | 22,890 | 5,020 | 4,270 | 9,290 |
| TOTAL | 496,270 | 91,960 (18%) |
101,880 (21%) |
193,840 (39%) |
44,950 (9%) |
257,480 (52%) |
302,430 (61%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
MSHCP Conservation Area Configuration Issues
Several large blocks of habitat supporting the few known foraging locations, and potential foraging locations of the merlin will be conserved as Criteria Area and Public/Quasi-Public, including the Prado Basin, Santa Ana River, Lake Mathews-Estelle Mountain, Wilson Creek, Mystic Lake/ San Jacinto Wildlife Area, and Lake Skinner/Diamond Valley Lake. Although there is little documented use by merlins of the Lakeview Mountains, Santa Rosa Plateau, Interstate 15 corridor from El Cerrito to the San Diego County line, and French Valley area, these areas are included in the MSHCP Conservation Area and could be used for migration. As identified above, the species occurs within the MSHCP Plan Area as a transient foraging and wintering species, and, as such, the MSHCP Conservation Area should provide adequate habitat for potential and recurring foraging areas. These MSHCP Conservation Area areas are linked as well, however the merlin, due to its ability to move long distances, may rely less on the linkages than other species.
Conservation Summary
In summary, conservation of this species will be achieved by the inclusion of at least 193,840 acres of suitable Conserved Habitat including agriculture (field crops), grassland, freshwater marsh, cismontane alkali marsh, playa and vernal pool, desert scrubs, Riversidean alluvial fan sage scrub, coastal sage scrub, peninsular juniper woodland and scrub, riparian scrub, woodland and forest, and oak woodlands and forest habitats. Additionally, although there are no Core Areas for this species, several large blocks of habitat supporting the few known foraging locations, and potential foraging locations of the merlin will be conserved in the MSHCP Conservation Area, including the Prado Basin, Santa Ana River, Lake Mathews-Estelle Mountain, Wilson Creek, Mystic Lake/ San Jacinto Wildlife Area, and Lake Skinner/Diamond Valley Lake. These habitats and areas provide potential foraging for the merlin during transient and winter visits. The current population size of the merlin is unknown and may vary from year to year.
INCIDENTAL TAKE
About 302,430 (61 percent) of potential habitat for the merlin will be outside the Criteria Area and Public/Quasi-Public Lands and individuals within these areas will be subject to Incidental Take consistent with the Plan. None of the major areas, Prado Basin, Santa Ana River, Mystic Lake/San Jacinto Wildlife Area, Lake Skinner/Diamond Valley Lake area, Wilson Valley, and Lake Mathews-Estelle Mountain, where the merlin has been observed in the past are outside the MSHCP Conservation Area.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The UCR location database includes approximately 34 records for the merlin within the Plan Area dated from 1987 to 1999. Approximately 24 records are relatively recent (within the past 10 years) and of these recent records, 15 are high precision records that can be accurately placed within the area. The habitat types associated with these recent and high precision data records include sage scrub, riparian, alkali playa, crop lands, woodland and forest, grassland, chaparral, and residential. The residential habitat records may reflect records that are either no longer extant or where the location is a small pocket of suitable habitat within or adjacent to a developed area or may represent a transient individual using the available habitat opportunistically or during a flight over the area in migration or for foraging.
The literature available on the merlin is moderate because it is a bird of prey and receives interest from the raptor specialists within the ornithological field. Most of the literature is focused on the natural history of the species, distribution, and relationships of the species with other falcons and birds of prey. A number of general ornithological reference treatments have been prepared for the species. Little information is available with respect to the Plan Area other than general distribution and occurrence information.
Habitat and Habitat Associations
The merlin uses a wide variety of habitats. Range-wide, merlin breed in open country (e.g., open coniferous woodland, prairie) and winter in open woodland, grasslands, cultivated fields, marshes, estuaries and sea coasts (AOU 1998). Within southern California, birds are often found in these same habitats and are rarely found in heavily wooded areas or over open deserts (Garrett and Dunn 1981). The merlin frequents coastlines, open grasslands, savannahs, woodlands, lakes, wetlands, edges, and early successional stages where it forages while flying at low levels for primarily avian species (Zeiner, et al. 1990). It ranges from annual grasslands to ponderosa pine and montane hardwood-conifer habitats. Dense tree stands may be used for cover and frequently are close to bodies of water. They may nest in small groves of deciduous trees adjacent to open areas for foraging. They frequently occur in areas with undulating topography (Sodhi, et al. 1993).
Biogeography
Merlin breed locally in North America from Alaska through most of Canada, eastward to Newfoundland southward to Washington and Maine. The species winters from the large majority of the breeding range southward to northern South America (AOU 1998; Sodhi, et al. 1993).
Zeiner, et al. (1990) summarize the distribution, abundance, and seasonality of the merlin within California as follows. It is an uncommon winter migrant from September to May. The merlin occurs in most of the western half of the state below 1,500 m (3,900 ft). It is a rare winter migrant in the Mojave Desert; a few records are from the Channel Islands. Numbers of the species have declined markedly in California in recent decades.
Known Populations Within Western Riverside County
The merlin apparently may occur locally as a very rare winter visitor throughout much of western Riverside County within suitable habitat. It is more frequently observed within the Plan Area as a spring and fall migrant/transient but even then, it is infrequently observed and has few records within the area. Areas that have been documented to be used by the merlin include the area in and around the Mystic Lake/San Jacinto Wildlife Area. A total of four birds have been recently observed wintering in this area (Michael Patten, Riverside County Editor for American Field Notes and Past Secretary, California Bird Records Committee, pers. comm., 1998). Additional observations have been made in the Jurupa Hills. The species appears to be sparsely and erratically located within the central portion of the Plan Area. Other locations where the merlin has been recorded include: Prado Park, Santa Ana River, Lakeview Mountains, Diamond Valley Reservoir, and Wilson Valley. Recently, a merlin was observed in December in the vicinity of Skunk Hollow (Hayworth, 1999, pers. obs.).
Biology
Genetics: The merlin is polytypic with 10 subspecies total and 3 located within North America. The phylogenetic relationship of the merlin to other falcon species is unclear. It has 40 chromosomes compared to a range of 48 to 52 for several larger Falco species and the American Kestrel (Sodhi, et al. 1993).
Diet and Foraging: The merlin feeds primarily on small birds usually weighing less than 50 grams; it also feeds on small mammals, reptiles, and insects (Sodhi, et al. 1993). Most studies report a specialization on one or two locally abundant species of small birds. The principal prey species is characterized as one of the most abundant species in the area; often is foraging away from cover making it more vulnerable to predation; and is in the 20 to 40 gram weight range (Sodhi and Oliphant 1993). It frequents shorelines in winter and catches shorebirds. It searches while flying at low levels; attacks with a short dive, or dash from above. It may capture prey on the ground or in the air, after direct pursuit. The young may rely upon insects while developing predatory skills (Zeiner, et al. 1990).
Daily Activity: The merlin exhibits year-long, diurnal activity (Zeiner et al. 1990).
Reproduction: The merlin does not breed in California; it breeds in Alaska and Canada. It uses an abandoned stick nest from a crow or magpie usually in a conifer but also in a deciduous tree. Occasionally it nests in cavities, cliffs, in a deserted building, on the ground, or in an old nest of another bird (Craighead and Craighead 1956, Brown and Amadon 1968). The clutch of 4-5 eggs is laid from late May into June. It incubates 28-32 days, and chicks fledge at about 24 days (Trimble 1972).
Survival: Most individuals have a short life span, with a maximum life span seldom exceeding eight years (Sodhi, et al. 1993). First year mortality is approximately 70 percent (Fox 1964).
Dispersal: Fledglings disperse from nest sites between 10 July and 9 August in Montana (Becker and Sieg 1985). More males than females return to breed in the natal areas. The mean natal dispersal distance is 4.1 kilometers for females and 3.0 kilometers for males (Sodhi, et al. 1993). The distances moved between successive breeding seasons varies greatly (Wiklund 1996). Fidelity to the breeding site was higher in males than females and females dispersed nearly three times as far as for males. For both genders, low reproductive success was associated with long dispersal distances (Wiklund 1996).
Socio-Spatial Behavior: The merlin defends nest sites during the breeding season and intraspecific nest intruders are aggressively chased off (Sodhi 1991). The nearest neighbor distances range from 161 to 4,669 meters in some areas (Sodhi, et al. 1992). The merlin is not rigidly territorial in the nonbreeding season, but is intraspecifically aggressive (Zeiner, et al. 1990).
Community Relationships: Potential avian predators are driven away as soon as they enter the territory; the merlin is particularly intolerant of accipiters (Fox 1964, Bent 1938, Oliphant 1974).
Threats to Species
Whereas F. c. columbarius, the subspecies most likely to be observed within the Plan Area, was formerly considered fairly common locally and in certain years (Grinnell and Miller 1944), the species as a whole is considered an uncommon migrant and rare winter visitor by Garrett and Dunn (1981). Although a population decline may have been partially the result of the alteration of suitable open habitats, the expressed effects of environmental contaminants on a raptor species cannot be dismissed as a causative factor. Because it feeds mostly on birds, the population numbers may have been reduced by pesticides (Remsen 1978). Most merlin populations are no longer affected by pesticide contamination and appear to be reproducing well. Currently, the loss of suitable habitat within important nesting site areas may be the major factor affecting merlin numbers (Cade 1982).
Special Biological Considerations
Three distinct subspecies of merlin, all readily identifiable in the field, have been recorded in southern California. Although all three subspecies could be found in the Plan Area, the nominate F. c. columbarius is the expected race. Although the species is uncommon in its winter occurrence, it can occur almost anywhere and thus it is difficult to predict suitable location and habitat preference.
The continued presence of environmental contaminants in the merlin is a cause of concern but at present does not appear to be a major factor controlling population size. The expansion of populations into urban habitats helps to maintain numbers and is an optimistic reflection of the health of these urban environments and the adaptability of the species. Merlins can be successfully bred in captivity and are currently being produced by a number of private breeders for falconry (Sodhi, et al. 1993).
Human disturbance activities may elicit various responses from wildlife and differences in persecution histories result in diverse wildlife responses to different activity types. The merlin is more likely to flush when approached by a human on foot than when approached by an automobile (Holmes et al. 1993). For merlins, walking disturbances on paved roads resulted in shorter flight distances than a similar disturbance on gravel roads. Presumably, raptors perched along paved roads have habituated to the greater traffic volume associated with paved roads. Alternatively, individuals with greater tolerance limits to disturbance may be using areas with greater disturbance levels. Spatial buffer zones are commonly used to protect nesting sites from disturbance, however, buffer zones for wintering raptors also could be effective if placed around sensitive foraging areas. From this study, a buffer zone that would prevent flushing by approximately 90 percent of the wintering individuals of the merlin would be set at 125 meters (Holmes et al. 1993).
LITERATURE CITED
AOU (American Ornithologists' Union). 1998. Check-List of North American Birds. Seventh Edition. American Ornithologists' Union, Washington, D.C. 829 pp.
Becker, D. M., and C. H. Sieg. 1985. Breeding chronology and reproductive success of Richardson's merlins in southeastern Montana. Raptor Research 19: 52-55.
Bent, A. C. 1938. Life histories of North American birds of prey. Part 2. U.S. Natl. Mus. Bull 170. 482pp.
Brown, L., and D. Amadon. 1968. Eagles, hawks and falcons of the world. 2 Vols. Country Life Books, London. 945pp.
Cade, T. 1982. The falcons of the world. Cornell University Press. Ithaca. N. Y.
Craighead, J. J., and F. C. Craighead, Jr. 1956. Hawks, owls and wildlife. Stackpole Books, Harrisburg, PA. 443pp.
Fox, G. A. 1964. Notes on the western race of the pigeon hawk. Blue Jay 22:140-147.
Garrett, K. and J. Dunn. 1981. Birds of Southern California: Status and Distribution. Los Angeles Audubon Society. 407 pp.
Grinnell, J. and A.H. Miller. 1944. The Distribution of the Birds of California. Pacific Coast Avifauna Number 27. Copper Ornithological Club, Berkeley, California. Reprinted by Artemisia Press, Lee Vining, California; April 1986. 617 pp.
Hayworth, A. 1999. Pers. obs. Dudek & Associates. Inc.
Holmes, T., R. L. Knight, and G. R. Craig. 1993. Responses of wintering grassland raptors to human disturbance. Wildlife Society Bulletin 21: 461-468.
Oliphant, L. W. 1974. Merlins - the Saskatoon falcons. Blue Jay 32:1-8.
Patten, Michael . 1998. Pers. comm. Riverside County Editor for American Field Notes and Past Secretary, California Bird Records Committee.
Remsen, J. V., Jr. 1978. Bird species of special concern in California. Calif. Dep. Fish and Game, Sacramento. Wildl. Manage. Admin. Rep. No. 78-1. 54pp.
Sodhi, N. S. 1991. Pair copulations, extra-pair copulations, and intraspecific nest intrusions in merlin. Condor 93: 434-437.
Sodhi, N. S., P. C. James, I. G. Warkentin, and L. W. Oliphant. 1992. Breeding ecology of urban merlins (Falco columbarius). Can. J. Zool. 70: 1477-1483.
Sodhi, N. S., and L. W. Oliphant. 1993. Prey use and selection by urban-breeding merlins. Auk 110: 727-735.
Sodhi, N. S., L. W. Oliphant, P. C. James and I. G. Warkentin. 1993. Merlin (Falco columbarius). In The Birds of North America, No. 130 (A. Poole and F. Gill, Eds.) . Philadelphia: The Academy of Natural Sciences; Washington, D.C.: The American Ornithologists' Union.
Trimble, S. A. 1972. Merlin, Falco columbarius. U.S. Dep. Inter., Bur. Land Manage., Wash., DC. Tech. Note No. 271. 41pp.
Wiklund, C. G. 1996. Determinants of dispersal in breeding merlins (Falco columbarius). Ecology 77: 1920-1927.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
mountain plover (Charadrius montanus)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
mountain plover (Charadrius montanus)
Status:
State: Species of Special Concern
Federal: Proposed for Listing as Threatened (Federal Register 64:7587), February 16, 1999). Also recognized as a Fish and Wildlife Service Region 1 Species of Management Concern and Partners in Flight Priority Bird Species. Listed as Vulnerable by the International Union of Nature and Natural Resources (IUCN)
GROUP DESIGNATION AND RATIONALE
Group 3
The mountain plover is narrowly distributed at relatively few locations within the Plan Area in suitable habitat. The mountain plover uses playas and vernal pool, grassland, and some agriculture habitats during the winter in the Plan Area. Although playa and vernal pool habitat is well identified for the Plan Area, it encompasses a relatively small portion. The remaining habitats, grassland and agriculture land, are well distributed within the Plan Area but the mountain plover uses only a small portion of what is available. This species occurs within Core Areas that it uses for its winter visits. It also requires specific habitat conditions within these Core Areas. Because the mountain plover requires specific conditions, occurs in few locations within a broad habitat category, and uses a well defined habitat that is narrowly distributed, this species will require site specific considerations, protection of preferred habitat, and species specific management conditions as a Group 3 species.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 6,710 acres of suitable habitat for the mountain plover including playa and vernal pool habitat.
Objective 2
Include within the MSHCP Conservation Area at least 4 Core Areas and interconnecting linkages. The Core Areas will consist of two "large" areas (at least 2,500 acres of suitable habitat: playa, grassland, fallow agriculture) and two smaller areas (at least 1,000 acres of suitable habitat). Core Areas shall include the following areas: San Jacinto River floodplain (Proposed Core 5, Existing Constrained Linkage C, Proposed Extension of Existing Core 4, and Proposed Constrained Linkage 19; 7,320 acres), Mystic Lake/San Jacinto Wildlife Area (Existing Core H; 17,470 acres), and the playa west of Hemet (Proposed Noncontiguous Habitat Block 7; 1,250 acres), and may include areas adjacent to Lake Elsinore (Subunit 7 of Elsinore Area Plan; 1,810 acres), Lake Skinner/Diamond Valley Lake (Existing Core C plus Proposed Extension of Existing Cores 5, 6, 7; 29,060 acres), and Lake Matthews (Existing Core C plus Proposed Extension of Existing Core 2; 23,710 acres).
SPECIES CONSERVATION ANALYSIS
Conservation Levels
The mountain plover forages predominantly in the playa and vernal pool habitat and in certain other open areas including open, steppe-like agriculture lands and grasslands (e.g., Garrett and Dunn 1981). Potential habitat for the mountain plover includes playas and vernal pools and select agriculture lands (e.g., fallow, recently burned) and grasslands. These areas are located within the Riverside lowlands Bioregions. Within the vegetation mapping for the Plan Area, the suitable open grassland and fallow agriculture field acreage and locations are not available, thus, for the purpose of the conservation analysis, potential habitat for the mountain plover includes playas and vernal pools within the Riverside Lowlands bioregion. Based on these habitats, the Plan Area supports approximately 7,870 acres of habitat for the mountain plover. Table 1 shows the conservation and loss of potential habitat for the mountain plover. Overall, approximately 6,710 acres (85 percent) of mountain plover habitat in the Plan Area would be conserved in Criteria Area or existing Public/Quasi-Public designations. In addition, a total of 27,470 acres (25 percent) of grassland and 15,410 acres (13 percent) of agriculture field crops within the Riverside Lowlands Bioregions would be conserved in Criteria Area or existing Public/Quasi-Public designations. These acreages have not been included in Table 1 below because only a portion is suitable habitat. More important for the conservation of the mountain plover is the location of the grassland and agriculture field crops and these areas will be included in the analysis of the Core Areas for this species below.
TABLE 1
SUMMARY OF HABITAT CONSERVATION FOR
MOUNTAIN PLOVER
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| Riverside Lowlands Bioregion | |||||||
| Playas and Vernal Pools | 7,870 | 3,820 | 2,890 | 6,710 | 0 | 1,160 | 1,160 |
| TOTAL | 7,870 | 3,820 (49%) |
2,890 (37%) |
6,710 (85%) |
0 (0%) |
1,160 (15%) |
1,160 (15%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
As described below under Data Characterization, 1 of the 10 recent point localities have a high location precision . The UCR location database is insufficient for conservation analysis, however distribution information is available within the literature and anecdotally and will be used for the analysis of the locations of the mountain plover. Based on the anecdotal and literature information described below, mountain plovers have occurred recently in western Riverside County in appropriate habitat bounded by Perris, the Mystic Lake area, and Nuevo; in the Domenigoni Valley; and in the vicinity of Winchester between Highway 79 and Interstate 215 (Patten 1998 pers. comm.). The Domenigoni Valley location is no longer in existence.
The available data are not adequate to fully determine the present (and future) distribution of this nomadic species within the MSHCP reserve system or to determine the future performance of the reserve system. In addition, small numbers of mountain plovers may be important to the conservation of the species. However, there are definable locations for focusing conservation efforts where the species is observed in larger numbers that would be essential for conservation of the species. One important core population area, as documented for 2001 (Cooper 2001) is located within the San Jacinto Wildlife Area, Mystic Lake, and San Jacinto Floodplain. This core population area is conserved by the MSHCP as Criteria Area or Public/Quasi-Public designations as identified below. The MSHCP Conservation Area will include a total of at least 4 Core Areas and interconnecting linkages. The Core Areas will consist of two "large" areas (at least 2,500 acres of suitable habitat: playa, grassland, fallow agriculture) and two smaller areas (at least 1,000 acres of suitable habitat). Core areas will include: San Jacinto River floodplain (Proposed Core 5, Existing Constrained Linkage C, Proposed Extension of Existing Core 4, and Proposed Constrained Linkage 19; 7,320 acres total with 5,350 acres of suitable habitat), Mystic Lake/San Jacinto Wildlife Area (Existing Core H; 17,470 acres with 1,690 acres of suitable habitat), and the playa west of Hemet (Proposed Noncontiguous Habitat Block 7; 1,250 acres entirely suitable habitat), and may include areas adjacent to Lake Elsinore (Subunit 7 of Elsinore Area Plan; 1,810 acres with 1,460 acres of suitable habitat), Lake Skinner/Diamond Valley Lake (Existing Core C plus Proposed Extension of Existing Cores 5, 6, 7; 29,060 acres - acreage of suitable habitat is not available but is greater than 2,300 acres), and Lake Mathews (Existing Core C plus Proposed Extension of Existing Core 2; 23,710 acres - acreage of suitable habitat is not available but is greater than 1,000 acres). Thus, the San Jacinto River floodplain area and Lake Skinner/Diamond Valley Lake constitute the two large Core Areas and Mystic Lake/San Jacinto Wildlife Area, playa west of Hemet constitute the small Core Areas. Additional small Core Areas are located at the grasslands at Lake Elsinore and Lake Mathews. The total acreage within the six Core Areas is 80,620 acres with at least 13,050 acres of suitable grassland, agriculture, and playa habitat (suitable habitat within the Lake Skinner/Diamond Valley Lake and Lake Mathews area could not be quantified).
Conservation of this species, due to its relatively high risk of extirpation from the Plan Area, requires species specific conservation measures. Mountain plovers have been identified as responding well to burned grassland in the fall and winter roost sites areas, as discussed below (Knopf 1996). Management measures that have been proposed and taken in other areas include burning the grasslands to attract the species on the wintering grounds. For the MSHCP Plan Area, grassland and agriculture areas within the reserve within the Core Areas will have a schedule established for burning in order to keep grass and agriculture crop remnants at a low height as preferred by the mountain plover. The playa areas tend to maintain a low height profile and are not recommended for burning. This species specific measure will maintain the habitat conditions in a preferable state for the mountain plover and may encourage their continued or possibly increased use of the reserve areas.
Reserve Configuration Issues
A block of well connected habitat supporting the current known locations, and several smaller blocks of habitat supporting potential foraging habitat of the mountain plover would be conserved as Criteria Area and public/quasi public, including the Mystic Lake/ San Jacinto Wildlife Area with adjacent playa habitat, and San Jacinto River floodplain, and playas west of Hemet as the primary focus areas and the grassland adjacent to Lake Elsinore, Lake Skinner/Diamond Valley Lake, and Lake Mathews as other potential habitat areas.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 6,710 acres of suitable Conserved Habitat and 4 Core Areas within large blocks of habitat in the MSHCP Conservation Area. The Core Areas will consist of two large and two small areas of at least 2,500 and 1,000 acres of suitable grassland, agriculture, and playa habitats, respectively. An additional two potential Core Areas also are included in the MSHCP Conservation Area. The current population size of the mountain plover is unknown, due to its nomadic wintering and transient movement habits and a paucity of focused surveys for the species. The conservation strategy for the species depends on the preservation to the extent possible of existing occupied habitat and the identification and management of additional suitable habitat throughout the Plan Area using fire as a management tool to create suitable habitat out of the agriculture lands within the MSHCP Conservation Area.
INCIDENTAL TAKE
The Incidental Take of the mountain plover is difficult to quantify due to our limited knowledge of its distribution and abundance within the Plan Area. The maximum level of Incidental Take of mountain plover can be anticipated by the loss of the number of acres of habitat that will become unsuitable for this species. About 1,160 acres (15 percent) of potential wintering habitat, composed of playa and vernal pool habitat, for the mountain plover will be outside the Criteria Area and Public/Quasi-Public designations and individuals within these areas are subject to Incidental Take consistent with the Plan. The Winchester area, historically a potential Core Area, is outside of the MSHCP Conservation Area, however this area may no longer function as a Core Area.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The UCR location database includes 17 records dated from 1887 to 1999. A total of ten of these records are relatively recent (within the past 10 years) and only one of these recent records are of high precision and could be accurately located within the Plan Area. The habitat type recorded for this and less precise data records includes residential or grassland which may be accurate given the status and behavior of the species.
There is a low to moderate amount of literature for this species owing to its rarity although a summary of the species has been recently prepared that documents much of the natural history and biological information recorded for this species. No controlled scientific studies have been conducted and little management information is available. Very little information on this species is available for the Plan Area other than general distribution and occurrence information.
Habitat and Habitat Associations
Range-wide, mountain plovers breed in dry, open, shortgrass prairies or grasslands and winter in shortgrass plains, plowed fields, open sagebrush areas, and sandy deserts (AOU 1998). In the breeding areas, the species appears to require relatively open areas with little vegetative cover where it forages for insects. In areas of fragmented prairies, it also nests on fallow and recently plowed ground. At locations where courting or breeding birds have the opportunity to use plowed versus prairie surfaces, they use both equally (Knopf 1996). Overall, it avoids high and dense cover. It nests in high-elevation grassland, often in blue grama and buffalo grass patches (Graul 1975). Within the winter range, the birds spend about 75 percent of their time on plowed fields but prefer heavily grazed annual grasslands or burned fields as well as other open little vegetated areas (Knopf 1996).
Within California, the mountain plover frequents open plains with low, herbaceous or scattered shrub vegetation; it may occur in areas with sparse shrub cover but avoids high and dense cover (Zeiner, et al. 1990). Within southern California, the largest numbers of birds occur in grasslands and agricultural areas in the interior (Garrett and Dunn 1981). Alkali playa habitat, both in composition and structure and location, is identified as an important habitat type of the mountain plover (Patten 1998 pers. comm.). It does not nest in California; it occurs within the state only during the wintering season.
Biogeography
Mountain plovers breed locally from extreme southern Alberta generally eastward to North Dakota southward to Wyoming and western Texas. Birds disperse widely across the western and southern Great Plains in the late summer and early fall (Knopf 1996). The species winters generally from California south to Baja California and southeasterly to Texas and northern mainland Mexico (Cogswell 1977; AOU 1998).
Zeiner, et al. (1990) summarize the distribution, abundance, and seasonality of the mountain plover in California as follows. The population is declining and very local; occasionally it is fairly common. It is a winter resident from September through March with peak arrival in November and is found on short grasslands and plowed fields of the Central Valley from Sutter and Yuba counties southward. It is also found in foothill valleys west of San Joaquin Valley, and in Imperial Valley. It winters below 1,000 meters (3,200 feet). In winter, flocks are regularly found on the Carrizo Plain, the western San Joaquin Valley, and Imperial Valley, and the Antelope Valley. Flocks may also occur, at least irregularly, in the Lucerne Valley and along the Colorado River (Garrett and Dunn1981).
Known Populations Within Western Riverside County
The mountain plover apparently occurs (or has occurred) locally throughout much of western Riverside County in suitable habitat which is generally defined as the central portion of the area typified by such habitat types as grassland, agricultural areas, and alkali playa. This species is a rare transient and very local winter visitant. The largest numbers winter in the vicinity of Lakeview and closer to the coast, it is most numerous in the Tijuana River Valley in San Diego County (Garrett and Dunn1981). Other isolated records for the species within the UCR database include Santa Ana River, March ARB, Lake Perris/San Jacinto Wildlife Area, Mystic Lake, San Jacinto River, and three low precision data locations in Hemet, San Jacinto, and Sun City. All but one of these location records is low precision.
Mountain plovers have occurred recently in western Riverside County in appropriate habitat bounded by Perris, the Mystic Lake area, and Nuevo; in the Domenigoni Valley; and in the vicinity of Winchester between Highways 79 and Interstate 215 (Patten 1998 pers. comm.). The Perris/Nuevo/Mystic Lake area, identified as the Lakeview area, is one of few locales in California where mountain plovers have been regularly recorded in recent years (Garrett and Dunn 1981). The most recent documentation identifies the San Jacinto Valley, considered the floodplain of the San Jacinto River, Mystic Lake and the San Jacinto Wildlife Area, as one of the few remaining areas left in southern California outside of the Imperial Valley that support winter flocks of mountain plover (Cooper 2001). This area, as defined by Cooper (2001) appears to coincide with the Core Area identified above by Patten (1998 pers. comm.) for the Perris area and by Garrett and Dunn (1981) for the Lakeview area. The Domenigoni Valley no longer exists as a valley and thus cannot be a Core Area. The area in the vicinity of Winchester may serve as a Core Area, however it has not been identified as such recently.
Biology
Genetics: There are no subspecies of the mountain plover that are recognized. The closest affinities probably are to the Old World Caspian plover, oriental plover and Eurasian dotterel which appear to constitute a super species (Knopf 1996).
Diet and Foraging: The mountain plover searches on the ground for large insects, especially grasshoppers (Graul 1976a). Individuals take mostly ground-dwelling invertebrates and winged invertebrates while on the ground. The mountain plover appears to be a general opportunist of invertebrate taxa (Knopf 1996, 1998). The species appears to require relatively open areas with little vegetative cover where it forages for insects. Generally, the mountain plover forages in extensive areas of disturbed ground surface or areas of short vegetation (less than 2 centimeters) with interstitial spaces of bare ground. Disturbed surface sites include prairie dog towns, kangaroo rat precincts, sites of heavy sheep or cattle grazing or concentrations, dirt or gravel roadbeds, recently plowed ground, and fallow fields (Knopf 1996).
Daily Activity: The mountain plover exhibits year-long, diurnal activity (Zeiner, et al. 1990). Birds may have a daytime roost site, often in a depression (Knopf 1996).
Reproduction: The species has been recorded for breeding in dry open shortgrass prairies or grasslands (AOU 1998; Graul and Webster 1976). Nesting occurs mainly in flat areas with at least 30 percent bare ground (Knopf 1996). The species is generally monogamous; pair bonds form at least 18 days prior to copulations (Knopf 1996). The pair bonds are only maintained during the breeding season where 83 percent of the males return to the previous year's territories, in contrast only 40 percent of females (Knopf 1996). However, both males and females return to the same breeding area (within 100-800 meters of the previous year's nest) during subsequent breeding seasons (Knopf 1996). Only one brood is raised per adult per season, although some pairs have two clutches if the first clutch fails (Knopf 1996). The species breeds from late April through June; peaking in late May (Bent 1929). The female lays an average clutch of three eggs (range = 1-4). In years of abundant food, males may incubate and brood the young while females lay another clutch, often tended by another male (Ehrlich, et al. 1988.)
Survival: Predation on the mountain plover limits chick survival the most with the number of chicks per nesting attempt surviving to migrate from breeding grounds ranging from 0.17 to 0.74 (Knopf 1996). Predation pressures are higher during drought years (Knopf 1996). A main predator, the swift fox, may limit mountain plover productivity in areas where it is abundant (Knopf 1996). One study states that the success of plovers in raising chicks appears related either to overall fox activity in the area or to how effectively the adult detected and distracted foxes, rather than being related to any recent landscape fragmentation (Knopf and Rupert 1996).
Recently calculated survival rates are similar to those reported 20 years ago, implying that the recent declines in population are not attributable to either long-term declines in nesting productivity or phenomena occurring at non-breeding locales (Miller and Knopf 1993). Survival on the wintering grounds has been calculated at 0.9996 (Knopf and Rupert 1995).
Dispersal: Mountain plover chicks leave the nest within three hours of hatching and can catch their own food by the evening after they are born (Knopf 1996). Fledged mountain plovers join loosely organized fall flocks that include both adults and young of the year. These flocks begin forming in mid-June in some areas. Both males and females return to the same breeding area in subsequent years with documented nesting 100 to 800 meters from a previous nest site (Knopf 1996). Migration behavior consists of short- to long-distance migrations, more east-west than north-south (Knopf 1996). Birds move in flocks of greater than 30 individuals (Knopf 1996).
Socio-Spatial Behavior: During the breeding season, mountain plover territories may overlap; in one study, three males occupied 16 hectares in Colorado (Knopf 1996). The home range of adults with broods averages at 56.6 hectares until the fledging of young (Knopf 1996). Nests are widely spaced within a nesting area. Graul (1975) found 21 nests/ 65 hectares (162 acres), with an average distance between nests of 140 meters (425 feet). It ranges widely in winter flocks, sometimes of 100, or more. Mean territory size in prairie grasslands in Colorado was 16 hectares (40 acres). It may occupy the same territory year after year (Graul 1975, 1976b). It defends its territory against conspecifics, larkspurs, and horned larks in breeding season. Usually it is not territorial in non-breeding seasons, but it may defend a small, mobile feeding space.
Community Relationships: Most mountain plover egg and chick losses are to predators (Knopf 1996).
Threats to Species
In the proposed rule to list the mountain plover as threatened, the U.S. Fish and Wildlife Service (1999) concluded that the conversion of grassland habitat, agricultural practices, management of domestic livestock, and decline of native herbivores likely primarily led to the recent, documented decline of mountain plovers. Formerly considered abundant in California (Grinnell and Miller 1944), the species has declined precipitously in recent years. For instance, there were 1,156 birds recorded on an Orange County Christmas Count in 1957 (Hamilton and Willick 1996); no plovers were detected anywhere in the County during the winter of 1997-1998 (California Department of Fish and Game 1998 unpublished data) despite formal and informal censuses of historically-occupied locales.
Although the population decline in the coastal plains of the region is attributable to the destruction of suitable open habitats (Garrett and Dunn 1981), impacts to breeding habitats and birds are occurring on the breeding grounds and likely have contributed to the observed local declines. The habitat of the mountain plover is, in particular, easily converted to other landscapes and human uses. Nests are often made in cultivated fields and there they are often destroyed by farm machinery if planting occurs in May (Knopf 1996). Of 46 nests found in cultivated fields, 31 failed, 70.9 percent due to farm machinery, whereas predation only accounted for 3.3 percent of failures (Shackford, et al. 1999). Most of the threats to the species appear to occur at the breeding grounds within the Great Plains region. A major shift in regional planting activity has created a reproductive sink for mountain plovers and may explain the annual rate of decline since 1966 (Knopf 1996).
Special Biological Considerations
The presence or absence of water apparently does not influence the distribution of this species (Grinnell and Miller 1944).
Mountain plovers respond well to burned grassland both in the spring for nesting and in the fall and winter for night roost sites (Knopf 1996). Management measures that have been proposed and taken include burning the grasslands to attract the species both on the wintering and breeding grounds. New construction and farming activities including plowing, have been limited seasonally to avoid the breeding season.
In winter habitats, birds prefer alkali flats which are presently rare, and although cultivated fields are used, birds may be dependent on Core Areas of native habitat in October and November especially (Knopf and Rupert 1995). Mountain plovers forage and roost in loose flocks of 2 to 1,100 birds with the average flock size increasing late in the year (Knopf and Rupert 1995). The average distance the flock moves each day is 1.17 kilometers/day with the movements of the flock and individuals being highly variable. Site fidelity of the wintering flocks appears to be poorly developed. Mountain plovers appear to be using the cultivated fields for wintering out of force rather than choice (Knopf and Rupert 1995). A study of survival rates recorded 20 years ago and those rates present today, showed them to be similar indicating that recent declines in plover populations are not attributable to longer-term declines in nesting productivity or phenomena occurring at non-breeding locales (Miller and Knopf 1993).
LITERATURE CITED
AOU (American Ornithologists' Union). 1998. Check-List of North American Birds. Seventh Edition. American Ornithologists' Union, Washington, D.C. 829 pp.
Bent, A. C. 1929. Life histories of North American shorebirds. U. S. Natl. Mus. Bull. 146.
California Department of Fish and Game. 1998. unpublished data
Cogswell, H. L. 1977. Water birds of California. Univ. California Press, Berkeley. 399pp.
Cooper, D. S. 2001. California Important Breeding Areas. Audubon California. Los Angeles.
Ehrlich, P. R., D. S. Dobkin, and D. Wheye. 1988. The birder's handbook. Simon and Schuster, New York. 785pp.
Garrett, K. and J. Dunn. 1981. Birds of Southern California: Status and Distribution. Los Angeles Audubon Society. 407 pp.
Graul, W. D. 1975. Breeding biology of the mountain plover. Wilson Bull. 87:6-31.
Graul, W. D. 1976a. The mountain plover's mating system. Colorado Field Ornith. J. 20:17-18.
Graul, W. D. 1976b. Food fluctuations and multiple clutches of the mountain plover. Auk 93:166-167.
Graul, W. D., and D. E. Webster. 1976. Breeding status of the mountain plover. Condor 78:265-267.
Grinnell, J. and A.H. Miller. 1944. The Distribution of the Birds of California. Pacific Coast Avifauna Number 27. Copper Ornithological Club, Berkeley, California. Reprinted by Artemisia Press, Lee Vining, California; April, 1986. 617 pp.
Hamilton, R. and D.R. Willick. 1996. The Birds of Orange County, California: Status and Distribution. Sea and Sage Press, Irvine, California. 150 pp. with appendices.
Knopf, Fritz L. 1996. Mountain Plover (Charadrius montanus) In The Birds of North America, No. 211 (A. Poole and F. Gill, eds.) The Academy of Natural Sciences, Philadelphia, PA and The American Ornithologists' Union, Washington, D.C.
Knopf, Fritz L. 1998. Foods of mountain plovers wintering in California. Condor, v.100, n. 2, 1998: 382-384.
Knopf, F. L. and J. R. Rupert. 1996. Reproduction and movements of Mountain Plovers breeding in Colorado. Wilson Bulletin, v. 108, n.1, 1996: 28-35.
Knopf, F. L. and J. R. Rupert. 1995. Habits and habitats of mountain plovers in California. Condor, v. 97, n.3, 1995: 743-751.
Miller, B. J. and F. L. Knopf. 1993. Growth and survival of mountain plovers. Journal of Field Ornithology, v.64, n.4, 1993:500-506.
Patten, M. 1998. Riverside County Editor for American Field Notes and Past Secretary, California Bird Records Committee, pers. comm.
Shackford, J. S., D. M. Leslie, W. D. Harden. 1999. Range-wide use of cultivated fields by Mountain Plovers during the breeding season. Journal of Field Ornithology, v.70, n.1, 1999. Winter,: 114-120.
U.S. Fish and Wildlife Service. 1999. Endangered and Threatened Wildlife and Plants: Proposed Threatened Status for the Mountain Plover. Federal Register, Volume 64, Number 30 (February 16, 1999); pages 7587-7601.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
mountain quail (Oreortyx pictus)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
mountain quail (Oreortyx pictus)
Status:
State: None
Federal: None
GROUP DESIGNATION AND RATIONALE
Group 1
The mountain quail has a reported wide distribution within all of the mountain ranges west of the deserts and of the northern interior of California. It predictably inhabits suitable montane chaparral and brushy vegetation within coniferous forests. This species has been recorded within the U.S. Forest Service lands. It may occur throughout a greater portion of suitable habitat within the MSHCP Plan Area, but no records exist in the MSHCP database. Other sources conclude it is widely distributed within suitable habitat. Because it predictably uses suitable brushy montane chaparral and occurs widely throughout the Plan Area, it should respond well to a landscape level of management.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 234,940 acres of suitable habitat including chaparral, oak woodland, and montane coniferous woodland within large blocks in the Desert Transition (27,000 acres), San Bernardino Mountains (8,490 acres), San Jacinto Mountains (126,160 acres) and Santa Ana Mountains (73,290 acres) Bioregions.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
For the purpose of the conservation analysis, potential habitat for the mountain quail includes chaparral, oak deciduous woodland and forest, and coniferous forest within the Bioregions of the Desert Transition, San Bernardino Mountains, San Jacinto Mountains, and Santa Ana Mountains. Because the brushy habitats within these Bioregions extend to the lower elevations, this provides not only foraging and nesting habitat in the montane areas where the species has been documented to occur, but also provides winter foraging areas for the species if they move downslope for some period of time. Although they are typically associated with chaparral habitat, as identified below they occur within deciduous woodland and conifer woodland within brushy areas and these habitats should be included in the analysis. For deciduous woodland and coniferous woodland that may not contain a brushy understory, the habitat may still be used by the mountain quail for transient or migrational movements. Based on these habitats, the Plan Area supports approximately 328,740 acres of potential habitat for the mountain quail. Table 1 shows the conservation and loss of potential habitat for the mountain quail. Overall, approximately 234,940 acres (71 percent) of potentially suitable habitat are present within the Desert Transition, San Bernardino Mountains, San Jacinto Mountains and Santa Ana Mountains Bioregions. These lands will be conserved in Criteria Area or existing Public/Quasi-Public Lands.
TABLE 1
SUMMARY OF HABITAT CONSERVATION - MOUNTAIN QUAIL
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| San Bernardino Mountains, San Jacinto Mountains, Santa Ana Mountains and Desert Transition Bioregions | |||||||
| Chaparral | 271,230 | 18,500 | 174,980 | 193,480 | 28,620 | 49,130 | 77,750 |
| Woodlands and Forests | 27,710 | 1,280 | 19,780 | 21,060 | 4,070 | 2,580 | 6,650 |
| Montane Coniferous Forest | 29,800 | 20 | 20,380 | 20,400 | 40 | 9,360 | 9,400 |
| TOTAL | 328,740 | 19,800 (6%) |
215,140 (65%) |
234,940 (71%) |
32,730 (10%) |
61,070 (19%) |
93,800 (29%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
For the mountain quail, conservation on the Santa Rosa Plateau may be important for maintaining a connection between the Santa Rosa Plateau Nature Reserve and the Santa Ana Mountains. MSHCP Conservation Area locations in these areas are generally surrounded by Rural/Mountainous designations. Potential development in these areas is anticipated to retain vacant areas that will provide for seasonal movement for this species. A total of 32,730 acres (10 percent) of potential habitat will be designated Rural/Mountainous, which will permit 1 DU/10, 20, or 40 acres depending on slope. Most of this land use designation is not within the Bioregions within which the mountain quail occurs.
This species primarily occurs within Forest Service lands in chaparral, oak woodland and forest, and coniferous forest habitats. Under the existing Forest Land allocation plan, these locations or habitats generally are located within the San Jacinto and San Mateo Canyon wilderness areas as well as in most of the grazing allotments.
As described above under Data Characterization, 10 point localities of 22 relatively recent records with a high mapping precision have been documented for the MSHCP Plan Area. Of these 10 locations 3 locations appear to be inside the Criteria Area and 2 are located within Public/Quasi-Public lands of the San Bernardino National Forest. A total of 5 of the locations are outside the Criteria Area and Public/Quasi-Public Lands. Conservation of this species should be considered from a landscape perspective due to the relatively large and wide-spread population. In addition, there are definable locations for focusing conservation efforts including the forest service lands within the San Bernardino National Forest and Cleveland National Forest that are composed of montane chaparral, conifer forest, deciduous forest, as well as lower elevation habitat.
MSHCP Conservation Area Configuration Issues
Several large blocks of habitat supporting or potentially supporting the mountain quail will be conserved as Criteria Area and Public/Quasi-Public land designations, including the montane chaparral, deciduous, and coniferous forests within the San Bernardino National Forest and Cleveland National Forest as well as areas in the lower elevations within the San Bernardino Mountains, Santa Ana Mountains, San Jacinto Mountains, and Desert Transition Bioregions. Some of the large blocks of habitat have not been mapped as containing mountain quail. However, these habitat blocks may contain potentially suitable habitat and could be occupied by mountain quail in the future. As such, the MSHCP Conservation Area will provide adequate large blocks of habitat containing montane chaparral, deciduous and coniferous woodland habitat with habitat linkages provided to connect these large blocks of breeding habitat to lower elevation areas for wintering use. Habitat linkages have been identified for this species at the Horsethief Canyon, Indian Canyon and the San Jacinto River linkages under Interstate 15. Habitat connections also are well established between the Cleveland National Forest and the Santa Rosa Plateau and the San Bernardino National Forest and the upper parts of the Wilson Creek drainage which then are linked to the Aguanga area.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 234,940 acres of suitable Conserved Habitat including chaparral, oak deciduous woodland and forest, and coniferous forest within the Bioregions of the Desert Transition, San Bernardino Mountains, San Jacinto Mountains, and Santa Ana Mountains. In addition, large blocks of habitat containing montane chaparral, deciduous and coniferous woodland habitat with habitat linkages provided to connect these large blocks of breeding habitat to lower elevation areas for wintering use are in the MSHCP Conservation Area.
INCIDENTAL TAKE
About 93,800 acres (29 percent) of potential habitat for the mountain quail will be outside the Criteria Area and Public/Quasi-Public designations and individuals within these areas will be subject to Incidental Take consistent with the Plan. Additionally, approximately 32,730 acres of potential habitat (10 percent) are designated Rural/Mountainous and individuals within these areas will be subject to Incidental Take consistent with the Plan.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The UCR location database includes approximately 31 records for the mountain quail within the Plan Area dated from 1916 to 1999. A total of approximately 22 records are relatively recent (within the past 10 years) and of these recent records, ten are high precision records that can be accurately placed within the area. The paucity of records within the database is likely due to the lack of reporting rather than the scarcity of the species (Gutierrez and Delehanty 1999). The habitat types associated with these recent and high precision data records include chaparral, montane coniferous forest, and Jeffery pine. The chaparral habitats may reflect wintering locations.
The literature available on the mountain quail is relatively low. It is focused on the natural history of the species. However, it is very limited and is generally within ornithological reference treatments that have been prepared for multiple avian species. Little information is available with respect to the Plan Area other than general distribution and occurrence information.
Habitat and Habitat Associations
The habitat for the mountain quail is generalized as shrub-dominated communities (Gutierrez and Delehanty 1999). The mountain quail is found in dense montane chaparral and brushy areas within coniferous forests, locally on lower slopes, in pinon-juniper-yucca associations, also sometimes locally in dense arborescent coastal chaparral dominated by Ceanothus spp., manzanita, and scrub oak (Garrett and Dunn 1981). The mountain quail may use early-successional stage shrub vegetation following fire, logging, or other disturbance (Gutierrez and Delehanty 1999). A total of 97 percent of mountain quail observations are in mixed evergreen forest and chaparral cover types (Brennan et al. 1987). It may occur in open forests and logged or burned over forests (Terres 1980). It is found seasonally in open brush stands within conifer and deciduous forest and woodland, and in chaparral (Zeiner, et al. 1990). For cover it uses shrubs, brush stands, and trees, particularly on steep slopes. The micro habitat use of the species includes a configuration of tall, dense shrubs which are in close proximity to water and escape cover (Brennan et al. 1987). Escape cover may constitute rock formations, boulders, or dead limbs from trees (Gutierrez and Delehanty 1999).
The microhabitat associations include stronger associations with dense vegetative cover than other quail species. The microhabitat structure is complex and varies across the habitat types. In four northern California habitats, the average distance to cover was 0.83 meters and to water was 131 meters, maximum shrub height was 2.4 meters and percent shrub cover was 45.8 percent (Brennan et al. 1987).
Biogeography
The species' range is from southern Washington and southwestern Idaho, south to northern Baja California (Weathers, 1983). It occurs in the mountain ranges of California, eastern Nevada, western Idaho, and was apparently unsuccessfully introduced into western Colorado (Terres 1980). The mountain quail occurs in all of the California mountain ranges west of the deserts and the mountains of the northern interior. It is a common to uncommon resident, found typically in most major montane habitats of the state occupying slopes at elevations ranging from 700 to greater than 3,000 meters. Their primary range is the Sierra Nevada, Cascade and Coast Ranges, but substantial disjunct populations occur in the inter-mountain West and Baja Peninsula The northernmost population is on Vancouver Island, British Columbia, where it was introduced. The southern portion of the species' range consists of the Transverse, Peninsular, and Southern Coastal Ranges of southern California, occurring as low as 700 meters (Guitierrez and Delehanty 1999).
The lack of data on the historical distribution and inadequate records of introductions make the interpretation of the original distribution difficult. The Columbia River may have been the historic northern range limit in the Coast and Cascade Ranges of Oregon. Regardless, there has been a significant decline in the inter-mountain West during the twentieth century (Gutierrez and Delehanty 1999).
Known Populations Within Western Riverside County
The mountain quail is known to occur in the San Jacinto Mountains, San Bernardino Mountains, and the Santa Ana Mountains. The species may move downslope during the winter months.
Biology
Genetics: No quantitative estimates of morphological or genetic geographic variation of the mountain quail have been published. Only a qualitative assessment of the variation within the entire range is available. The mountain quail of the northern climates and humid coastal forests is the darkest and more brown; to the more southern areas, it is lighter and more gray dorsally. Five subspecies are currently recognized by the American Ornithologists Union, however, the subspecies delineation is based on poorly defined comparative and ill-marked plumage characters, therefore, both subspecies designations and subspecies ranges are considered dubious (Gutierrez and Delehanty 1999).
Diet and Foraging: The main foods taken by the mountain quail are predominately plant material for individuals of all ages throughout the year (Gutierrez and Delehanty 1999). The mountain quail eats green foliage, buds, acorns, flowers, fruits, and seeds of forbs, shrubs, and trees; and also some arthropods (Zeiner, et al. 1990). Typically, invertebrates make up approximately 0 to 5 percent of the diet and rarely does this exceed 20 percent. The mountain quail depends on the seeds, fruits, and flowers of perennial plants in its primary California range (Gutierrez and Delehanty 1999). It gleans, scratches, plucks, grazes, and browses on and around the foliage. It forages in the shrub and forest communities under the canopy and at the edge of these habitats, rarely venturing far from cover but at greater distances than when not foraging. The average distance from protective cover while foraging was 1.5 meters. It can meet its water needs from food and dew in cool weather, but requires drinking water in dry weather. The species may gather at water sources in the summer, and the brood of young may be found no more than 0.8 kilometers (0.5 mile) from water for several days (Zeiner, et al. 1990).
Daily Activity: The mountain quail exhibits year-long, diurnal activity (Zeiner et al. 1990).
Reproduction: The mountain quail nests on the ground in herbage at the base of a tree, in rocks, or near shrubs, logs, or stumps. It breeds in late March to late August; most nests are active in May through July. One clutch is produced per year with an average of 10 eggs and a range of 6-15 eggs. The female incubates about 25 days, while the male remains nearby. Both genders tend the precocial young. The brood may remain together through the winter (Zeiner, et al. 1990).
Survival: No information is available or was reviewed.
Dispersal: The mountain quail may migrate upslope and downslope up to 32 kilometers (20 miles). It usually breeds at higher elevations, and moves downslope for winter, following the snow line (Zeiner, et al. 1990).
Socio-Spatial Behavior: Mountain quail population densities have been documented in northern California to range from 9 to 30 birds per 100 hectares (Brennan, et al. 1987). In Idaho, the home range averaged about 2.6 km2 in a sedentary population (Ormiston 1966). Few movements of the species exceeded 0.8 kilometers in summer. An area is not defended for the territory, but male aggression increases as the pair forms in the spring. In California, a breeding pair occupied 2-20 hectares (5-50 acres) (Johnsgard 1973).
Community Relationships: Miller and Stebbins (1964) suggested coyotes, rattlesnakes, Cooper's hawks, and bobcats are potential predators of the mountain quail, especially at water sources (Zeiner et al. 1990). Coveys are composed of family groups, nonbreeding adults, or aggregations of families formed during the nonbreeding season. Adults may form coveys during the nonbreeding years. Mountain and California quail occasionally form mixed flocks, particularly during the nonbreeding season. Single individuals of each species are reported within coveys of the other species for relatively long periods (up to several weeks). During the breeding season, adults of each species may exhibit agonistic behavior toward adults and young of other species (Gutierrez and Delehanty 1999).
Threats to Species
Loss of habitat due to human developments may be a threat and heavy grazing can destroy habitat (Zeiner, et al. 1990). Analyses of both long-term and short-term Breeding Bird Survey data found stable populations in California, Oregon, and Washington (Gutierrez and Delehanty 1999). The highest abundance of birds is recorded in California, particularly in the Sierra Nevada. The mountain quail was once widespread and common in Idaho, but, according to published and unpublished survey data, hunter returns, and anecdotes, near extirpation occurred in the second half of the twentieth century. Declines are associated with degradation of riparian and brush habitat due to livestock grazing, fire exclusion, and water development (Gutierrez and Delehanty 1999).
Special Biological Considerations
The mountain quail migrates from high elevation areas where breeding occurs to lower protected valleys and, therefore, must have unrestricted access to migratory corridors. A 1987 study attempted to use mountain quail as an indicator species for an ecological guild of birds (Block, et al. 1987). This attempt resulted in varied results within and among vegetation types suggesting that indicator species should only be used where guild members share the same habitat and habitat variation is minimal.
Development of water sources in arid areas can increase habitat use by the species (Zeiner, et al. 1990). Wildlife "guzzlers" in the Mojave Desert receive significant use by adult mountain quail with broods during the dry summer and fall months. Livestock watering tanks in arid regions may also benefit quail, especially if an exit ramp is provided to minimize drowning.
Logging may be a possible benefit by forest conversion to shrub cover and other early seral stage vegetation. Limited brush removal may stimulate growth of food plants (Gutierrez and Delehanty 1999).
LITERATURE CITED
Block, W. M., L.A. Brennan and R. J. Gutierrez. 1987. Evaluation of guild-indicator species for use in resource management. Environmental Management 11: 265-270.
Brennan, L.A., W. M. Block and R. J. Gutierrez. 1987. Habitat use by mountain quail in northern California [USA]. Condor 89: 66-74.
Garrett, K., and J. Dunn. 1981. Birds of Southern California, status and distribution. Los Angeles Audubon Society. Los Angeles, California. 408pp.
Grinnell, J. and A. H. Miller. 1944. The Distribution of the birds of California. Pacific Coast Avifauna No. 27. Artemesia Press. Lee Vining, California. 615pp.
Gutierrez, R. J. and D. J. Delehanty. 1999. Mountain Quail. The Birds of North America 457: 1-27.
Johnsgard, P. A. 1973. Grouse and quails of North America. Univ. Nebraska Press, Lincoln. 553pp.
Miller, A. H., and R. C. Stebbins. 1964. The lives of desert animals in Joshua Tree National Monument. Univ. California Press, Berkeley. 452pp.
Ormiston, J. H. 1966. The food habits, and movements of mountain quail in Idaho. M.S. Thesis, Univ. Idaho, Moscow. 39pp.
Terres, J. K. 1980. The Audubon Society encyclopedia of North American birds.
Weathers, W. 1983. Birds of Southern California's Deep Canyon. University of California Press, Los Angeles. 266 pp.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
Nashville warbler (Vermivora ruficapilla)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
Nashville warbler (Vermivora ruficapilla)
Status:
State: None
Federal: None
Forest Service: None
GROUP DESIGNATION AND RATIONALE
Group 2
The Nashville warbler has been recorded in the literature and within the UCR database in the San Bernardino National Forest within the Plan Area as a likely breeding bird. It is widely distributed but uncommon during migration periods. Core breeding season areas are few and important to conservation of the species. In the Plan Area, two core breeding season areas have been identified, Lake Fulmor and Pine Cove. Additional observations within the Plan Area primarily occur in lowland Bioregions and probably represent spring or fall transients. Because the Nashville warbler uses a variety of habitats within montane Bioregions for breeding (including chaparral, riparian, deciduous woodland, and coniferous woodland), occurs in a variety of habitats for migrant movements in all Bioregions (including brush and scrub habitats, desert scrub, and wooded habitats), and has specific locations that are identified as core breeding season areas, it is included in Group 2.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 209,490 acres of suitable breeding habitat including chaparral, montane coniferous forest, riparian scrub, woodland, and forest, and oak woodlands in montane Bioregions.
Objective 2
Include within the MSHCP Conservation Area at least three Core Areas. Core Areas will include the known breeding locations at Lake Fulmor and Pine Cove (represented by MSHCP Conservation Areas within the San Bernardino National Forest; 149,750 acres) and one additional breeding area identified within the MSHCP Conservation Area.
Objective 3
Include within the MSHCP Conservation Area at least 209,290 acres of suitable dispersal or migration habitat and interconnecting linkages, including chaparral, coastal sage scrub, desert scrubs, Riversidean alluvial fan sage scrub, and oak woodland and forest for dispersal during migration. These habitats will be conserved in all Bioregions of the Plan Area but do not include the acreage included in Objective 1.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
For the purpose of the conservation analysis, breeding habitat for the Nashville warbler includes montane breeding habitats within the mountain Bioregions, including chaparral and woodland (riparian scrub, woodland, and forest, oak woodland and forest, and montane coniferous forest) components. Suitable dispersal or migration habitat for the Nashville warbler includes chaparral, coastal sage scrub, desert scrubs, Riversidean alluvial fan sage scrub, and oak woodland and forest in all Bioregions of the Plan Area. Based on these habitats, the Plan Area supports approximately 659,350 acres of potential habitat for the Nashville warbler. Table 1 shows the conservation and loss of potential habitat for the Nashville warbler. Overall, approximately 418,780 acres (64 percent) of potential habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public lands. A total of 209,490 acres of suitable breeding habitat within the San Bernardino Mountains, San Jacinto Mountains, and Santa Ana Mountains Bioregions habitats will be conserved . Suitable dispersal and migration habitat will include at least 209,290 acres including chaparral, coastal sage scrub, desert scrubs, Riversidean alluvial fan sage scrub, and oak woodland and forest in all Bioregions of the Plan Area but does not include the acreage counted as breeding habitat in order to avoid double-counting.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
NASHVILLE WARBLER
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| All Bioregions | |||||||
| Chaparral | 413,470 | 64,900 | 207,370 | 272,270 | 59,580 | 81,620 | 141,200 |
| Coastal Sage Scrub | 152,690 | 47,160 | 34,560 | 81,720 | 26,240 | 44,730 | 70,970 |
| Desert Scrub | 9,360 | 3,670 | 1,310 | 4,980 | 40 | 4,340 | 4,380 |
| Montane Coniferous Forest | 29,890 | 20 | 20,480 | 20,500 | 40 | 9,350 | 9,390 |
| Riparian Scrub, Woodland, Forest | 14,610 | 3,920 | 7,270 | 11,190 | 370 | 3,050 | 3,420 |
| Riversidean Alluvial Fan Sage Scrub | 7,150 | 3,170 | 2,060 | 5,230 | 220 | 1,700 | 1,920 |
| Oak Woodlands and Forests | 32,180 | 2,390 | 20,500 | 22,890 | 5,020 | 4,270 | 9,290 |
| TOTAL | 659,350 | 125,230 (19 %) |
293,550 (45 %) |
418,780 ( 64%) |
91,510 ( 14%) |
149,060 (23 %) |
240,570 (36 %) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
This species occurs within the Forest Service lands in the San Bernardino National Forest as a breeding bird and may occur within the Cleveland National Forest. It also may migrate through the Forest Service lands in the spring and fall. It occurs predominantly within chaparral, coastal sage scrub, alluvial fan sage scrub, riparian scrub, woodland and forest, oak woodland and forest, and montane coniferous forest within these lands as a breeding or migrating species. Under the existing Forest Land allocation plan, these locations and habitats generally are located within the San Jacinto Wilderness Area, San Mateo Canyon Wilderness Area, the roadless areas, and in most of the grazing allotments as well. The Nashville warbler has been documented to have a potential core breeding population area within the Lake Fulmor and Pine Cove areas of the San Bernardino National Forest. It may also occur in other core breeding areas within the San Bernardino National Forest due to presence of suitable habitat, although locations have not been documented due to low survey effort or lack of reporting. Conservation of the two known core breeding locations as well as other core breeding areas that are identified by the Forest Service as a result of additional focused surveys for the species on Forest Service lands is an important conservation strategy for this species.
In addition to the above protection, the Riparian/Riverine Areas and Vernal Pools policy described in Section 6.1.2 of the MSHCP Volume I, provides for conservation of wetlands which provide foraging and perhaps breeding habitat at higher elevations for this species through avoidance and minimization. Mitigation for impacts to wetlands shall be incorporated in accordance with the "No Net Loss" policy of federal and state wetland regulations. The proposed mitigation shall be directly related to the functions and values of the wetland as related to this species and result in equivalent replacement. This policy will provide protection for foraging and breeding habitat of the Nashville warbler in the riparian areas.
As described below under Data Characterization, 8 of the 22 relatively recent point localities have a high precision. Of these 8 point localities, 2 will be inside the Criteria Area and 2 are located within Public/Quasi-Public Lands. Two point locations will be in the Rural/Mountainous zone. The 2 high precision recent points located outside the MSHCP Conservation Area, are located in non-native grassland observed during migration due to the lowland location. The data point locations are highly under-represented due to lack of reporting. Nashville warbler is observed frequently especially during migration but has also been documented in the National Forest areas (Hayworth, 1999, pers. obs.). Conservation of this species will be considered from a landscape perspective due to the fact that the suitable habitat has been well defined and the species is very flexible in utilizing foraging habitats during the migration movements. Providing additional suitable habitat that is not currently occupied may assist with the recovery of the species. In addition, there are definable locations for focusing conservation efforts including potential breeding habitat in the San Jacinto Mountains, Santa Ana Mountains, and San Bernardino Mountains. As identified above, there are two known and likely breeding areas within the San Bernardino National Forest including the Lake Fulmor area and Pine Cove area.
Rural/Mountainous Designation Areas
As depicted on the MSHCP Plan Map (Figure 3-1, MSHCP Volume I), certain areas adjacent to or in proximity to the MSHCP Conservation Area are designated as Rural/Mountainous in the County's General Plan. These areas are generally constrained for development due to steep topography and the level of development in these areas is anticipated to be of a low density, rural residential character. While these areas will not be included within the MSHCP Conservation Area or managed for the benefit of species conserved under the MSHCP unless it is necessary to conserve the species as prescribed above, low levels of development anticipated in these areas outside of essential core breeding areas may provide an edge to the MSHCP Conservation Area that may be of value to certain species. For the Nashville warbler, conservation of the Santa Rosa Plateau, Sage area, and the Badlands may be important as a spring and fall migratory movement area. MSHCP Conservation Area locations in these areas are generally surrounded by Rural/Mountainous designations. Potential development in these areas is anticipated to retain vacant areas, and wetlands in particular due to the Riparian/Riverine Areas and Vernal Pools policy, which will provide foraging and migratory movement habitats for the Nashville warbler. A total of 91,510 acres (14 percent) of potential habitat will be designated Rural/Mountainous.
MSHCP Conservation Area Configuration Issues
Several large blocks of habitat supporting or potentially supporting the Nashville warbler will be conserved as Criteria Area and Public/Quasi-Public designations, including the breeding habitat within the San Bernardino Mountains and the San Jacinto Mountains, potential breeding habitat within the Santa Ana Mountains, and migratory stopover or movement areas at the Prado Basin/ Santa Ana River, Temescal Wash, Lake Mathews-Estelle Mountain, Sedco Hills, Santa Rosa Plateau Nature Reserve, Vail Lake/Wilson Valley, Temecula, Murrieta, and Tucalota creeks, Sycamore Canyon Regional Park, and Box Springs. Some of the large blocks of habitat have not been mapped as containing Nashville warblers possibly due to lack of survey effort or lack of reporting. However, these habitat blocks have suitable foraging habitat and movement habitat and within the higher elevations contain suitable breeding habitat and could be occupied by Nashville warblers in the future. As a long-distance migrant, Nashville warblers are likely able to discover and use patches of habitat that have not been documented to be used in the past. As such, the MSHCP Conservation Area will provide adequate blocks of a variety of upland and riparian habitat within the San Jacinto, San Bernardino, and Santa Ana mountains Bioregions as core breeding areas for this species and blocks of a variety of upland and riparian habitat for spring and fall transient movements within the lower elevation Bioregions.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 418,780 acres of suitable Conserved Habitat for breeding and dispersal/migratory movements. In addition, three Core Areas, including Pine Cove and Lake Fulmor plus one additional location within the Forest Service or MSHCP Conservation Area, will be conserved within the MSHCP Conservation Area. The MSHCP has been designed to preserve the large blocks of areas that contain a variety of potentially suitable habitats for foraging use during migration as well as blocks of currently unknown sizes that contain potentially suitable nesting habitat for the species.
INCIDENTAL TAKE
About 240,570 acres (about 36 percent) of potential breeding and dispersal/migration habitat for the Nashville warbler will be outside the Criteria Area or Public/Quasi-Public designations, and individuals within these areas will be subject to Incidental Take consistent with the Plan. The area outside the MSHCP Conservation Area includes 71,100 acres of breeding habitat within the mountain Bioregions and 169,470 acres of dispersal/migration habitat. Of this, approximately 91,510 acres (14 percent) of potential habitat are located within Rural/Mountainous designation areas. While the Rural/Mountainous areas are not included within the MSHCP Conservation Area and will not be managed for the benefit of wildlife, the anticipated levels of development in these areas will likely be consistent with maintaining some habitat for the Nashville warbler. Two point locations will be in the Rural/Mountainous zone. Two high precision recent points are located outside the MSHCP Conservation Area and are located in non-native grassland observed during migration due to the lowland location. The known nest location areas are not outside the MSHCP Conservation Area.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The location database for the Nashville warbler includes 29 data records dated from 1900 to 1999. Of the 22 more recent records (since 1990), a total of eight are of high precision. Two of these records are recorded for residential areas and may no longer exist, the balance are recorded in non-native grassland, sage scrub, and riparian. One record is located in the montane coniferous forest and one is within deciduous woodland at high elevation which reflect potential breeding locations. All other records are for migrating individuals.
A low-to-moderate amount of literature is available for the Nashville warbler, mostly relating to general natural history and warblers in general. Few controlled scientific studies have been conducted and little management information is available. Very little information is available for the Plan Area other than what is available regarding basic distribution information.
Habitat and Habitat Associations
The Nashville warbler, as a whole, prefers second growth, open deciduous, or mixed species forests, with a high level of light penetration preferably with shrubby undergrowth. It is never found in unbroken forest habitats (Williams 1996).
The Nashville warbler appears to require heterogenous second-growth forests and shrubs and most frequently uses branches for nesting but also makes considerable use of leaves and twigs (Sodhi and Paszkowski 1995). This species most commonly breeds in pine, hardwood and conifer forests in the Sierras and in montane chaparral habitats in southern California, and in general, this includes second growth, open deciduous, or mixed species forests, with high levels of light penetration and shrubby undergrowth (Williams 1996; Ziener et al. 1990). In summer habitat in the San Gabriel and San Bernardino Mountains, where breeding is presumed but not observed to occur, individuals are found on shaded slopes within mixed coniferous forests with California black oaks and yellow pines and brush communities with manzanita (Bent 1953; Garrett and Dunn 1981).
During migration, the western population of the Nashville warbler frequents drier habitats, sometime in mountains areas in both deciduous and coniferous trees, along forest edges, and in bands of conifers. It may occur in sage dominated habitats (Williams 1996). The Nashville warbler also is generally seen migrating through lowland woodland and riparian habitats (Zeiner et al. 1990). During migration, it also is observed moving through desert habitats and although individuals do not appear to prefer a particular vegetation type, they have been frequently observed moving through tall trees (Miller and Stebbins 1964).
The wintering habitat is primarily low deciduous open forests and suburban gardens but may also include a wide variety of habitats such as cloud forest, tropical deciduous forest, disturbed deciduous forest, thorn forest and pine-oak-fir forest (Williams 1996).
Biogeography
Two disjunct populations of the Nashville warbler breed in North America: one east of the Mississippi River and a second in the northwestern United States (Williams 1996). The breeding range extends from southern Canada to central California and northern midwest states of the United States (Terres 1980). The western population breeds from southern interior British Columbia and north and northwest Washington south through the Cascade Range into northwest and southwest Idaho and northwest Montana, also in central and southern Oregon along the Cascade Range, east to Hart Mountain into northern California south along the Coast Range and western slope of the Sierra Nevada and in the extreme west-central Nevada (Williams 1996). The Nashville warbler has been recorded regularly in the summer in small numbers in the San Gabriel and San Bernardino Mountains and in the Mount Pinos area although nesting activity has not been confirmed (Garrett and Dunn 1981).
The Nashville warbler winters in Mexico, southern Texas, southern Florida down through Guatamala; some may winter in coastal lowlands of southern California (Williams 1996; Terres 1980). It is a highly migratory species, breeding in North America and wintering typically in Mexico and generally it leaves the breeding territories in August and departs from winter territories to arrive on breeding grounds in April (Williams 1996).
Zeiner, et al. (1990) has summarized their seasonal movements as follows. It usually arrives in California in April and quickly becomes common on breeding areas; it gradually leaves the mountains in September; a few linger occasionally in coastal locations into early winter; there are a few records of overwintering along the coast. The Nashville warbler occurs in coastal and desert lowlands of southern California during migratory movements (Zeiner et al. 1990).
There is no information on historical changes in the distribution of the Nashville warbler (Williams 1996). Current status of the Nashville warbler is not threatened in either breeding or winter range. Both long-term and short-term continent-wide Breeding Bird Survey trends of population size show no clear pattern of population increase or decrease. For the western population only, a long-term trend shown a 1.6 percent increase in British Columbia (Williams 1996).
Known Populations Within Western Riverside County
In southern California, breeding populations have been reported to not occur south of San Bernardino and Los Angeles counties (Zeiner et al. 1990). A breeding population may be present in northern Riverside county within the San Bernardino Mountains or within the San Jacinto Mountains (Zeiner, et al. 1990). The species occurs within all Bioregions of the Plan Area commonly as a spring migrant or transient and less commonly as a fall migrant or transient (Garrett and Dunn 1981).
Geographic locations recorded within the U.C. Riverside database include: Santa Ana River, Moreno Valley, Lake Mathews-Estelle Mountain, Lake Elsinore, Wildomar, Sedco Hills, Temecula Creek, Wilson Creek, Motte-Rimrock Reserve, and Banning for nonbreeding locations, and San Bernardino National Forest for presumed breeding locations. Locations within the San Bernardino National Forest that potentially represent breeding locations include an area near Pine Cove and Lake Fulmor.
Biology
Genetics: The Nashville warbler occurs as two geographically separated subspecies located in the eastern and central North America and one located in western North America (Williams 1996).
Diet and Foraging: The Nashville warbler feeds almost entirely on insects, such as tent caterpillars, brown-tail moths, gypsy moths, leafhoppers, aphids, flies, and grasshoppers, gleaned from all canopy levels and also hawked from the air (Zeiner et al. 1990). The Nashville warbler is a major predator of the Douglas-fir tussock moth in Oregon, Idaho, and California (Torgersen and Mason 1987).
In the Sierra Nevada, it prefers feeding in black oak and later in the season forages in softer shrubs especially deerbrush (Airola and Barrett 1985). In the west, the Nashville warbler is found foraging predominately in forest trees, at low to mid-tree height, mostly foraging among the foliage, sometimes among the twigs. It is also found in low shrub foliage (Williams 1996). It forages at the end of branches, at the tips of vegetation among twigs, in tassels of flowering trees, and on undersides of leaves, particularly in hardwoods (Williams 1996).
Daily Activity: The Nashville warbler exhibits year-long diurnal activity; it is a nocturnal migrant (Zeiner, et al. 1990). Males and females contribute equally to feeding young during the day, however time of day shows differences in feeding rates probably reflecting a difference in diurnal behavior patterns between males and females (Knapton 1985)
Reproduction: Airola and Barrett (1985) have shown that the Nashville warbler prefers to nest in oaks (Quercus spp.), but also uses deerbrush (Ceanothus integrimus) in a portion of the Sierras. Within the forests these birds tend to place their nest on open ground at the base of a shrub in a generally dry and sandy plateaus with nearby oaks, spruce, fir, aspens, white birch, white pines or redwood (Lawrence 1948). The nest may be sunk in moss on or very near the ground, and is built of mosses, stems of ferns, pine needles, rabbit fur, and lined with rootlets, fine grasses, pine needles, and hairs of deer or moose (Terres 1980).
Eggs of the Nashville warbler are laid from May through August and number four to five, incubation lasts for 11 to 12 days and the young first fly about 11 days after hatching (Terres 1980). To adapt to a short summer and breeding season, Nashville warblers mate on the wintering grounds or during migration as evidenced by presence of sperm in the females cloaca (Quay 1986). The pairs breed solitarily; both parents tend to the young and the young breed the following year (Zeiner, et al. 1990).
Survival: Total nest success of the Nashville warbler over a two year period was calculated at 2.87 fledglings per total nests monitored (Williams 1996). One female was recovered at age 7 years 3 months (Klimkiewicz et al. 1983). No other information was available in the literature.
Dispersal: Fledglings of the Nashville warbler have been observed foraging on their own and joining mixed-species flocks from July to the end of the summer resident period (Williams 1996). No other information was available in the literature.
Socio-Spatial Behavior: In one population, in Ontario, Lawrence (1948) reported an average territory size of 0.5 acre. No other information was available on territories in the western populations or on territoriality during the migrating period or at the wintering grounds.
Community Relationships: As a relatively common bird, a short line transect was able to detect population differences in the Nashville warbler population sizes at different sites (Hanowski et al. 1990). The Nashville warbler occurs in mixed flocks within a tropical deciduous forest in western Mexico during the nonbreeding season. The Nashville warbler and blue-gray gnatcatcher were characterized as nuclear species in these nonbreeding foraging flocks (Hutto 1994).
Threats to Species
The Nashville warbler is uncommonly subject to cowbird parasitism and predation from small mammals, accipiters and snakes (Zeiner, et al. 1990; Lawrence 1948).
Both the long-term and short-term continent-wide Breeding Bird Survey trends show no clear pattern of population increase or decrease, however in the western population and especially in British Columbia there may be a slight increase in the population which may be resulting from newly available habitat in regenerating clear cuts (Williams 1996). As a species favoring second-growth and cut-over areas, the Nashville warbler may actually benefit from cutting and lumbering in its breeding range and may be less vulnerable to habitat change than many other neotropical migrants (Williams 1996).
Because riparian habitats in western United States are among the habitat most modified by humans, there is a potential for decline of Nashville warblers using these habitats (Williams 1996). The effect of riparian habitat declines may affect the migrating population if it uses such habitats during its movements from breeding to wintering grounds (Williams 1996).
Special Biological Considerations
In one area of western Oregon, a population has been observed increasing despite clear-cutting activities (Williams 1996).
Nashville warblers were observed in greater numbers in the logged areas of early-successional forests when compared to burned areas. The logged areas contained higher densities of live trees, more live tree species and wider size ranges of live trees (Schulte and Niemi 1998). The Nashville warbler was ranked as 1 (lowest potential) of 10 most vulnerable to extirpation based on geographic range, population size, reproductive potential, susceptibility to cowbird parasitism, migratory status, and diet specialization (Reed 1995).
LITERATURE CITED
Airola, D. A. and R. H. Barrett. 1985. Foraging and habitat relationships of insect-gleaning birds in a Sierra Nevada mixed-conifer forest. Condor 87:205-216.
Bent, A. C. 1953. Life histories of North American wood warblers. U.S. National Museum Bulletin 203. 734pp.
Garrett, K. and J. Dunn. 1981. Birds of southern California. Los Angeles Audubon Society. 408pp.
Hanowski, J. M. G. J. Niemi, and J. G. Blake. 1990. Statistical perspectives and experimental design when counting birds on line transects. Condor 92: 326-335.
Hayworth, Anita.. 1999. Pers. obs.
Hutto, R. L. 1994. The composition and social organization of mixed species flocks in a tropical deciduous forest in western Mexico. Condor 96: 105-118.
Klimkiewicz, M. K., R. B. Clapp, and A. G. Futcher. 1983. Longevity records of North American Birds: Remizidae through Parulinae. J. Field Ornithol. 54: 287-294.
Knapton, R. W. 1985. Parental feeding of nestling Nashville warblers: the effects of food type, brood size, nestling age and time of day. Wilson Bulletin 96: 594-602.
Lawrence, L de K. 1948. Comparative study of the nesting behavior of chestnut-sided and Nashville warblers. Auk 65:204-210.
Miller, A. H. and R. C. Stebbins. 1964. The lives of desert animals in Joshua Tree National Monument. University of California Press, Berkeley. 452pp.
Quay, W. B. 1986. Sperm release in migrating wood-warblers nesting at higher latitudes. Wilson Bulletin 97: 283-295.
Reed, J. M. 1995. Relative vulnerability of extirpation of montane breeding birds in the Great Basin. Great Basin Naturalist 55: 342-351.
Schulte, L. A. and G. J. Niemi. 1998. Bird communities of early-successional burned and logged forest. J. Wildlife Management 62: 1418-1429.
Sodhi, N. S. and C. A. Paszkowski. 1995. Habitat use and foraging behavior of four parulid warblers in a second-growth forest. J. Field Ornithology 66: 277-288.
Terres, J. K. 1980. The Audubon Society Encyclopedia of North American Birds. Alfred A. Knopf, New York, New York. 1109pp.
Torgersen, T. R. and R. E. Mason. 1987. Predation on egg masses of the Douglas-fir tussock moth. Environmental Entomology 16: 90-93.
Unitt, P. 1984. The birds of San Diego County. San Diego Society of Natural History: Memoir 13, San Diego, California. 276pp.
Williams, J. M. 1996. Nashville Warbler (Vermivora ruficapilla). In The Birds of North America, No. 205 (A. Poole and F. Gill, eds.). The Academy of Natural Sciences, Philadelphia, and The American Ornithologists' Union, Washington, D.C.
Zeiner, D.C., W. F. Laudenslayer, K. E. Mayer and M. White eds. 1990. California's Wildlife: Volume II - Birds. California Department of Fish and Game. Sacramento, California. 732pp.
northern goshawk (Accipiter gentilis)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
northern goshawk (Accipiter gentilis)
Status:
State: Species of Special Concern
Federal: Federal Special Concern species; Partners in Flight Priority Bird Species; Species of Management Concern; USDA Forest Service Region 5 Sensitive; San Bernardino National Forest Sensitive
GROUP DESIGNATION AND RATIONALE
Group 2
The northern goshawk has been observed in two nest locations within the MSHCP Plan Area. There is an additional potential nest site within Tahquitz Valley and it has generally been documented as occurring as a breeding bird between an elevation of 2,000 to 2,700 meters (Garrett and Dunn 1981). It may occur as a transient migrant almost anywhere else within the Plan Area, has been found in semi-wooded areas in the lowlands, and has been recorded as a migrant within the vicinity of Hemet. The northern goshawk is widely distributed outside of the Plan Area within North America, but not in southern California. Due to its requirements for a large territory as a large predatory bird, it would not be expected to have a large population as a nesting species within the Plan Area and within its preferred habitat. It is well studied and documented for using mature forest lands. This species is considered to be a Group 2 species because its conservation requires integration of habitat and site specific requirements.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 34,020 acres of suitable nesting and wintering habitat including oak woodland and forest and montane coniferous habitat within the San Bernardino Mountains and San Jacinto Mountains Bioregions. These Bioregions provide the suitable nesting elevation of 2,000 to 2,700 meters as well as lower elevation habitat for wintering.
Objective 2
Within the MSHCP Conservation Area, protect and buffer from disturbance the 2 known nest sites (Lake Fulmor and San Jacinto Wilderness area), the possible nest site within Tahquitz Valley and any additional nesting locations. Protection is the conservation of at least 1.6 square kilometers of suitable nesting habitat within the MSHCP Conservation Area around each known nest. Buffering of the nest sites will include limiting human activities within a 250 meter radius around each of the nest site locations during the breeding season.
Objective 3
Within the MSHCP Conservation Area, maintain (once every three years), the continued use of, and successful reproduction at a minimum of 75 percent of the known nesting localities. Successful reproduction is defined as a nest which fledged at least one known young.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
For the purpose of the conservation analysis, potential habitat for the northern goshawk includes deciduous woodland and forest, and coniferous montane forest within the San Bernardino Mountains and San Jacinto Mountains Bioregions. Breeding has been documented to occur at elevations from 2,000 to 2,700 meters (Garrett and Dunn 1981). The area within which the species has been generally documented in the past includes Tahquitz Valley, Willow Creek, Skunk Cabbage, Humber Park, and Fulmor Lake (Garrett and Dunn 1981). 1998 records show two breeding pairs: one pair in the Fulmor Lake /Lawlor Lodge area and one pair in the vicinity of the San Jacinto Wilderness area in the San Jacinto Mountains (Michael Patten, Riverside County Editor for American Field Notes and Past Secretary, California Bird Records Committee, pers. comm., 1998). These two sites have been documented to have been in use for approximately the past 20 years (USFS pers. comm. 1999). It may occur as a transient migrant almost anywhere within the Plan Area, has been found in semi-wooded areas in the lowlands, and has been recorded within the vicinity of Hemet in November (Garrett and Dunn 1981).
The deciduous woodland and forest and montane coniferous forest habitats within the San Bernardino Mountains and San Jacinto Mountains Bioregions provide not only foraging and nesting habitat in the montane areas and elevations (2,000 to 2,700 meters) where the species has been documented to occur, but also provides winter foraging areas for the species if they move downslope for some period of time. Based on these habitats, the Plan Area supports approximately 46,290 acres of potential habitat for the northern goshawk. Table 1 shows the conservation and loss of potential habitat for the northern goshawk. Overall, approximately 34,020 acres (73 percent) of potential habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public Lands.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
NORTHERN GOSHAWK
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| San Bernardino Mountains and San Jacinto Mountains Bioregions | |||||||
| Woodlands and Forests (oak) | 16,490 | 300 | 13,320 | 13,620 | 850 | 2,020 | 2,870 |
| Montane Coniferous Forest | 29,800 | 20 | 20,380 | 20,400 | 40 | 9,360 | 9,400 |
| TOTAL | 46,290 | 320 (<1%) |
33,700 (73%) |
34,020 (73%) |
890 (2%) |
11,380 (25%) |
12,270 (27%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
As described above under Data Characterization, 2 point localities, both relatively recent (1987 and 1995) and with high precision have been documented for the MSHCP Plan Area. It appears that one location is within the U. S. National Forest land adjacent to Fulmor Lake/Lawlor Lodge and the other is within the San Jacinto Wilderness area adjacent to a private land holding. There are additional records in the literature for the Tahquitz Valley area, Willow Creek, Skunk Cabbage, Humber Park (Garrett and Dunn 1981). These locations have not been confirmed by the UCR database or by the USFWS. Conservation of this species should be considered from a landscape perspective as well as a site-specific location perspective due to the overall sensitivity of the nest site locations. Providing additional suitable habitat that is not currently occupied may assist with the recovery of the species. In addition, there are definable locations for focusing conservation efforts including the Forest Service lands within the San Bernardino National Forest that are composed of montane coniferous forest, deciduous forest and the known nest site locations at Fulmor Lake/Lawlor Lodge, in the vicinity of the San Jacinto Wilderness area in the San Jacinto Mountains, and the potential nest site location at Tahquitz Valley.
MSHCP Conservation Area Configuration Issues
Several large blocks of habitat supporting or potentially supporting the northern goshawk will be conserved as Criteria Area and Public/Quasi-Public Land designations, including the montane coniferous forests and deciduous woodland within the San Bernardino National Forest and Mt. San Jacinto State Park and including lower elevation areas to provide wintering habitat. Habitat blocks that currently are not documented to be occupied by the northern goshawk may contain suitable habitat and could be occupied by northern goshawks in the future. As a species with a large foraging area, northern goshawks are likely able to discover and use patches of woodland or coniferous habitat that have not been documented to be used in the past. As such, the MSHCP Conservation Area provides adequate large blocks of habitat as Core Areas around the currently known nest sites of the species as well as other large blocks of potentially suitable habitat that may be occupied in the future for nesting, foraging, or for wintering.
This species primarily occurs within Forest Service lands in deciduous woodland and montane coniferous habitat within the San Jacinto Mountains Bioregion. The area within which the species has been generally documented in the past includes Tahquitz Valley, Willow Creek, Skunk Cabbage, Humber Park, and Fulmor Lake (Garrett and Dunn 1981). Under the existing Forest Land allocation plan, these locations and habitats generally are located within the San Jacinto Wilderness area.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 34,020 acres of suitable Conserved Habitat including oak woodland and forest and montane coniferous forest within the San Jacinto Mountains and San Bernardino Mountains Bioregions. In addition the known nest site locations at Fulmor Lake/Lawlor Lodge, in the vicinity of the San Jacinto Wilderness area in the San Jacinto Mountains, and the potential nest site location at Tahquitz Valley are within the MSHCP Conservation Area.
INCIDENTAL TAKE
About 12,270 acres (27 percent) of potential habitat for the northern goshawk will be outside the Criteria Area and Public/Quasi-Public and individuals within this habitat will be subject to Incidental Take consistent with the Plan. No nest sites are known outside the MSHCP Conservation Area; however no systematic surveys have been conducted to locate nest sites for this species outside the MSHCP Conservation Area. No take of active nest sites will be permitted.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The UCR location database for the northern goshawk and information from the USFWS indicates that there are two known nesting locations within the San Bernardino National Forest. It is not likely there are substantially more locations although the species may occur within the Plan Area as a transient in very low numbers and at unpredictable locations. The two locations were recorded in 1987 within oak woodland and in 1995 within Jeffrey pine forest.
A moderate amount of literature is available for the northern goshawk because it is a bird of prey and is of interest from a community perspective in relation to potential competition with congeners. Most of the literature pertains to general natural history, niche determination, and the accipiters in general. Few controlled scientific studies have been conducted. However, some management studies are available and timber harvest recommendations have been reported. Very little information is available for the Plan Area other than the 3 point localities.
Habitat and Habitat Associations
Northern goshawks typically nest in moderately dense montane forests that are broken by lakes, streams, meadows, or openings. Nests are usually concealed in dense stands of trees, however the stands may consist of small groves of large pines, firs, or aspens (Gaines 1988). The goshawk prefers middle and higher elevations and mature, dense conifer forests but nests in most forest types are found throughout the geographic range from sea level to the alpine elevations (Squires and Reynolds 1997).
Goshawks selected foraging sites that had higher canopy closure, greater tree density, and greater density of trees than on neighboring control plots (Squires and Ruggiero 1996). These correlations are consistent with the hypothesis that goshawk morphology and behavior are adapted for hunting in moderately dense, mature forests, and that prey availability (as determined by the occurrence of favorable vegetation structure where prey are present above a low threshold) is more important than prey density in habitat selection (Beier and Drennan, 1997).
Nesting habitat of the northern goshawk includes mature, mixed hardwood-hemlock stands of birch, beech, maple, and eastern hemlock within the eastern portion of its range. In the central portion, it nests primarily in ponderosa pine. In the western portion of its range, the goshawk nests in Douglas-fir, various pines, and aspen. The forest stands containing nests are often small, approximately 10 to 100 acres and territories may contain one to five alternative nest site areas (Squires and Reynolds 1997). In northern California, the maximum distance between alternative nest stands was 1.8 kilometers and approximately 85 percent of alternate nest stands were less than 0.7 kilometer apart (Squires and Reynolds 1997).
Goshawks select productive old-growth forests, with greater than 60 percent of all adult goshawk relocations occurring in this cover type. Non-forest, clear cut, and alpine cover types were least used by the northern goshawk and were avoided relative to their availability. The median breeding season minimum convex polygon use areas of adult goshawks was about 10,000 acres (Iverson, et al. 1996).
In saturated populations, the species composition and structure of vegetation in the nest areas depends on the availability within a given territory. Thus, although the goshawk may prefer certain nest habitat structures, habitat characteristics in the nest areas vary from territory to territory, depending on the availability. Although the species is considered a habitat generalist at a large spatial scale, they tend to nest in a relatively narrow range of vegetation structural condition. Nests are typically in mature to old growth forests composed primarily of large trees with high, 60 to 90 percent, canopy closure, near the bottom of moderate hill slopes, with sparse ground cover. These closed stands may reduce predation and along with the north slopes, provide relatively cool environments (Squires and Reynolds 1997).
In California, the species may casually occur in winter along the coast, throughout the foothills, and in the northern deserts where it may be found in pinyon-juniper and low-elevation riparian habitats (Zeiner, et al. 1990). In general, for cover purposes, it uses mature and old-growth stands of conifer and deciduous habitats. Dense, mature conifer and deciduous forest, interspersed with meadows, other openings, and riparian areas also are required. Nesting habitat of the species includes north-facing slopes near water (Zeiner, et al. 1990).
Biogeography
Northern goshawks breed in North America locally from Alaska eastward to Newfoundland southward to southern California, New Mexico, mainland Mexico, Baja California, central Mexico, and the Gulf Coast (AOU 1998). Specifically, they breed from western and northern portions of central Alaska, north-central Yukon, northern Ontario, and Newfoundland south along the Pacific Coast and Atlantic coast to southern Canada, excluding southeastern Alberta, southern Saskatchewan and southern Manitoba. Within the western United States, the goshawk breeds from the mountains of northern and western Washington south through the mountains of western Oregon and California. It also breeds from western and southern Montana and Idaho south through Wyoming, Utah, and the western half of Colorado to north central and southwestern New Mexico and into northwestern Arizona. In the eastern United States, it breeds from the Canadian border south to east-central Minnesota, northern Wisconsin the northern portion of Michigan, central Pennsylvania, northwestern New Jersey, southeastern New York to Massachusetts (Squires and Reynolds 1997).
The species winters primarily within the breeding range (AOU 1998). Studies suggest that northern goshawk migrations and wintering area selections are primarily dictated by prey availability (Squires and Reynolds 1997; Craighead and Craighead 1956). During irruption years, larger numbers may winter outside of the breeding range and travel greater distances and reach southern California, the Lower Colorado River, northern Texas, central Oklahoma, Arkansas, Tennessee, and central Virginia (Squires and Reynolds 1997).
Within California, the northern goshawk breeds in the north coast ranges through the Sierra Nevada, Klamath, Cascade, and Warner Mts., and possibly in Mt. Pinos and San Jacinto, San Bernardino, and White Mts. The species remains year-long in breeding areas as a scarce to uncommon resident. It prefers middle and higher elevations, and mature, dense conifer forests (Mallette and Gould 1978; Zeiner, et al. 1990). The northern goshawk is an uncommon permanent resident in the mountains of California in the Sierra Nevada south at least as far as Tulare County and in the Coast Range south as far as Mendocino County (Grinnell and Miller 1944). Within southern California, the species breeds only in Ventura County (e.g., Mount Pinos, Mount Abel), the San Bernardino Mountains, and the San Jacinto Mountains (Garrett and Dunn 1981). It is casual in occurrence in winter along the coast, throughout the foothills, and in the northern deserts, where it may be found in pinyon-juniper and low-elevation riparian habitats (Zeiner, et al. 1990).
Some movement downslope may occur after the breeding season, as far as valley foothill hardwood habitat in the Sierra Nevada. Migration into lowlands occurs irregularly and is probably related to availability of food rather than weather (Mallette and Gould 1978).
Known Populations Within Western Riverside County
Currently the northern goshawk is a very rare resident in southern California including the Plan Area (Garrett and Dunn 1981). The area within which the species is generally documented is between 2000 and 2,700 meters and localities include Tahquitz Valley, Willow Creek, Skunk Cabbage, Humber Park, and Fulmor Lake (Garrett and Dunn 1981). 1998 records show two breeding pairs: one pair in the Fulmor Lake /Lawlor Lodge area and one pair in the vicinity of the San Jacinto Wilderness area in the San Jacinto Mountains (Michael Patten, Riverside County Editor for American Field Notes and Past Secretary, California Bird Records Committee, pers. comm., 1998). These 2 pairs have been documented for approximately the past 20 years (USFS pers. comm. 1999). Within the entire southern California area, the northern goshawk occurs in very low numbers. It may occur as a transient migrant almost anywhere within the Plan Area and has been found in semi-wooded areas in the coastal lowlands and has been recorded within the vicinity of Hemet in November (Garrett and Dunn 1981).
Biology
Genetics: A presumed natural hybrid of the Cooper's hawk and northern goshawk was reported by Gray in 1958 (Terres 1980).
Diet and Foraging: The northern goshawk hunts in wooded areas. Its uses snags and dead-topped trees for observation and prey-plucking perches. Typical prey items of the northern goshawk are of a wide diversity and the species is considered an opportunist. It feeds mostly on birds, from robin to grouse in size. Small mammals, of squirrel and rabbit size, are often taken. The goshawk rarely eats carrion and insects ( Schnell 1958). Prey items of the goshawk include: tree squirrels, hares, grouse, corvids, woodpeckers and large passerines, with reptiles and insects making up a more occasional portion of the accipiter's diet (Squires and Reynolds 1997). In general, they have been documented to take a variety of small to small/medium mammals and birds from small passerines to ducks and pheasants (Bent 1937). Based on biomass, the snowshoe hare and grouse account for a very large proportion of the diet in the Cascade region of Washington; this population has a narrower niche than some populations but demonstrates the opportunistic behavior of the species relative to prey selection (Watson et al. 1998). Prey are caught in the air, on the ground, or in vegetation, using a fast, searching flight, or rapid dash from a perch. The goshawk is fierce, aggressive and very persistent in pursuing prey and is capable of tremendous short bursts of speed when chasing a prey animal (Brown and Amadon 1968).
Similar to the other accipiter species, the goshawk is a bird of the woodland, either deciduous or coniferous and sometimes mixed with cultivation. It is not averse to crossing clearings or entering them to hunt and will forage relatively large distances. Frequently, they migrate away from nesting or resident areas in response to food availability (Brown and Amadon 1968). Beier and Drennan (1997) found that several habitat structure components were more influential in foraging site selection than prey density. They found that goshawks select sites with higher canopy closure and greater tree density. These results are consistent with the hypothesis that goshawk behavior and morphology are adapted for hunting in moderately dense mature forests where prey are most vulnerable (Squires and Reynolds 1997).
In California, mature and old-growth habitat are used for foraging, whereas open habitats such as meadows and seedling and sapling stands are avoided (Austin 1993). It was also found that nest sites and surrounding home range areas had greater basal area, canopy cover, and trees in large diameter classes than did random plots, however, some populations readily forage in open habitats (Hargis, et al. 1994).
Daily Activity: The goshawk is a diurnally active species (Zeiner, et al. 1990). Young have been reported bathing (Bond 1942, Brown and Amadon 1968).
Reproduction: The nesting sites of the goshawk vary in different parts of the country. In the northwest, it commonly nests in mature douglas fir, ponderosa or lodgepole pine of varying densities. They also nest in cottonwoods and other deciduous trees in stream bottoms (Call 1978). The nest habitat is single to multistoried, depending on the forest type. In eastern deciduous forests, goshawks prefer to nest in large forested areas containing more mature timber than generally present in the landscape. In northern California, smaller nest stands (less than 10 hectares) containing one to two nests were occasionally occupied, whereas the occupancy of large stands (greater than 20 hectares) was more consistent and thus the occupancy rate of nest stands was positively correlated with stand size (Squires and Reynolds 1997).
The goshawk usually nests on north slopes, near water, in the densest parts of stands, but close to openings (Jackman and Scott 1975). In eastern Oregon, the nest usually is located in the fork of a large, horizontal limb close to the trunk, at the bottom of the live canopy 6-24 m (19-82 ft) above ground. The species uses large, live trees with a mean diameter at breast height of 27.4 cm (11 in) (Reynolds, et al. 1982). It uses old nests, and maintains alternate sites. Within the southern California forests, they usually nest in large live trees, frequently on north slopes near water, in the densest part of the stand, but also near openings (USFS pers. comm. 1999). Multistoried forest canopy predominates at nest sites; however, there is typically no shrub layer. The nest site and nest tree tend to be comprised of the locally dominant tree species (Hall 1993). Nest tree height and diameter support the body size predictions about nesting habitat for accipiter hawks. As a result of this, it is difficult to differentiate between Cooper's hawk and northern goshawk nest sites for most site variables. Many of the commonly used forest stand characteristics such as basal areas and total tree density may not be adequate for predicting suitable accipiter nesting habitat (Siders and Kennedy 1996).
The nest is a large, flat, untidy structure placed usually in a crotch, but sometimes out on a limb (Harrison 1978). It is usually at a height of 30 to 60 feet in a variety of trees, and the species may actually prefer hardwood in some areas (Shuster 1980). At least in some areas the nests are lined with hard pieces of bark and also with green sprigs of conifers. One to five, usually three eggs are laid. The clutch size is affected by the abundance of favorable prey. The latest dates for egg-laying are the early part of June. Incubation is done by both male and female for approximately 41 days. The young become independent at approximately 70 days (Brown and Amadon 1968; Bond 1942.).
These accipiters are thought to be monogamous with a 1:1 sex ratio prior to fledging. Mate retention is high for both males and females and it is thought that the pair remain together as long as both are alive, at least in areas where the species is non-migratory (Brown and Amadon 1968; Squires and Reynolds 1997). In most cases, one clutch is produced per year (Squires and Reynolds 1997).
Survival: Estimated mortality rates based on banding recoveries are 66 percent for year one; 33 percent for year two; 19 percent for year three; 19 percent for year four and 11 percent for the following years (Squires and Reynolds 1997).
Dispersal: Dispersal typically occurs 65 to 95 days after hatching (Squires and Reynolds 1997). Fledglings remain within their respective nest stands for most of the post-fledging period and movements away from the nest tree are initially restricted by the size of the nest stand itself (Shipman and Bechard 1995). Nestlings from banding studies relocated as breeders nesting 16.1 to 24.2 kilometers from their natal site (Squires and Reynolds 1997).
Some breeding populations appear to be either migratory or exhibit transient movements. A group of northern goshawks moved approximately 65 to 185 kilometers during the winter season and then returned to the previous year's nesting area in the spring (Squires and Ruggiero 1995).
Socio-Spatial Behavior: Home range appears to be the same as territory. The northern goshawk is extremely defensive of the nest area. It is vociferous; it will strike intruders, including humans. The territory is estimated to be 1.6 to 39 sq. km (0.6 to 15 sq mi) (Brown and Amadon 1968), and average 2.1 sq. km. (0.8 sq. mi.) in Wyoming (Craighead and Craighead 1956). Distances of 2.9 to 5.6 km (1.8 to 3.5 mi) have been reported between nesting pairs. They have an indefinite nesting area, varying in size from six to 15 miles often containing several nests among which they may choose (Brown and Amadon 1968). In California, the maximum distance between alternative nest stands is 1.8 kilometers and approximately 85 percent of the alternate nest stands are less than 0.7 kilometers apart. Depending on the continuity of forest cover, nests of adjacent pairs occur at regular intervals (Squires and Reynolds 1997). Distances between pairs have been reported to be 3.0 to 5.8 kilometers (Zeiner, et al. 1990).
Community Relationships: A study of the spotted owl (Strix occidentalis) in Washington state found that "nests originally made by northern goshawks were the most common nest type used by spotted owls (55.3 percent)" (Buchanan, et al. 1993). They are known to prey on other hawk and owl species and will defend their territory from other species of raptors (Squires and Reynolds 1997). Great horned owls, ravens, and crows may prey on young goshawks. The species may be limited by competition for food with other accipiters (Jones 1979).
Threats to Species
Shooting and trapping, as well as pesticide effects on eggshell thickness have not been thought to affect this species. Since most of the habitat of this species is within public lands such as National forests and national parks, there is comparatively little threat in the way of habitat destruction, but both falconry and logging are potential threats (Remsen 1978). Each year, nests are destroyed by logging operations but the impacts to the nesting populations are unknown. It is not known to what extent logging in California has affected this species, which requires moderate to dense stands of pine or fir for breeding. Harvest methods that create large areas of reduced forest canopy cover may be especially detrimental; however, forest harvest may be compatible with goshawk management provided that habitat needs are available at multiple spatial scales. In one study in California, nesting densities remained fairly high despite fragmentation of mature forests through timber harvest; however, territories associated with large contiguous forest patches were more consistently occupied compared to highly fragmented stands. Although nesting frequently occurs in areas impacted by timber harvest, the long term viability of these populations is unknown (Squire and Reynolds 1997).
Northern goshawks may be relatively intolerant of human presence near their nests which has led to breeding failures in the Yosemite Park area (Gaines 1988).
Special Biological Considerations
Although petitions have been filed to list the northern goshawk as threatened or endangered, there appears to be no evidence to support the claim that the population has declined (Kennedy 1997). The majority of the data on abundance of breeding pairs indicate that goshawk densities are highly variable spatially and temporally. There is some evidence to suggest that abundance is correlated with food availability. Thus, fecundity is apparently influenced by a combination of food availability and predation rates (Kennedy 1997).
This secretive species is reported infrequently and the total population breeding within California is probably quite small (Remsen 1978). Birds may move downslope during winter months and fall migrants or winter visitors of uncertain origin have been observed in fall and winter months in coastal and desert areas outside of montane breeding areas (Garrett and Dunn 1981). While present in such areas, goshawks typically have occupied open woodlands (Grinnell and Miller 1944).
Timbering activities near nest sites has been shown to cause failure when activities are conducted near a nest site (Squires and Reynolds 1997). The probability of persistence of goshawks has declined in some areas over the past 50 years owing to habitat loss and likely will continue to decline under current management plan regimes; however, the goshawk population likely is not in immediate peril. A study of conservation attempts in southeast Alaska concluded that long rotation forestry (e.g., 300 years) and uneven-aged silvicultural management will best maintain sustainable populations of goshawks (Iverson, et al. 1996). Although habitat reserves are not considered an essential component of a forest-wide goshawk conservation strategy, reserves, in combination with extended rotations, may be important where the intensity of past management actions has precluded the opportunity to attain a desired combination of forest age classes achievable under long rotations. Reserves are most likely critical if extensive clear cut logging continues (Iverson, et al. 1996).
Silvicultural guidelines have been developed for the management of Douglas-fir forests stands for both saw timber production and goshawk nesting habitat (Lilieholm, et al. 1993). On average timber-growing stands reach goshawk habitat suitability when the stand height is 25 meters at age 75 and provide 65 years of goshawk nesting habitat until the final harvest at age 140. Approximately 1,320 cubic meters per hectare may be harvested over this rotation scenario.
The northern goshawk has been used as an indicator species for canopied, old-growth forests by the U.S. Forest Service since 1982 (Shipman and Bechard 1995). As a top level carnivore, the density of breeding pairs is low and density varies among populations. Productivity of the species varies between years on the same Plan Areas and among landscapes within a limited geographic area. The prey availability strongly affects the occupancy and productivity of the species. There is limited understanding of how predation, competition, landscape alteration, or food availability regulate northern goshawk populations (Squires and Reynolds 1997).
Management agencies usually attempt to reduce disturbance during the nesting period by delineating protected areas around the nest trees. However, buffer areas of small and large size (up to 200 hectares) still appear to be inadequate to provide nesting protection. Occupancy of nest areas dropped by 80 percent in logged areas with large buffers (Crocker-Bedford 1990). Of special management concern are providing forest conditions for supporting diverse prey populations (Squires and Reynolds 1997). Consequently, attention needs to be given to the general habitat over the entire foraging range of a pair of goshawks, because nest buffers by themselves are ineffective. Where management goals include both timber harvests and goshawks, the suggested method of Crocker-Bedford (1990) is to practice silviculture that maintains prime goshawk habitat (dense large trees with open undertsory) within the foraging range of nests (> 2,000 hectares). It is also critical to maintain dense habitat in large enough blocks to inhibit open-forest and edge-benefitted raptors. The watershed surrounding the nest location should be divided into thirds, with the nest concentration at the junction of the thirds. The first third, 1,000 to 2,000 hectares, should be regenerated over the first one-third of the extended rotation period. The second 1,000 to 2,000 hectares should be regenerated over the second third of the rotation period, and so on. As a result, at any one time, a 1,000 hectare to 2,000 hectare block near a territory's nest should be in prime foraging habitat while a second block would be in marginal foraging habitat. This method may potentially provide goshawks with a competitive advantage over edge-benefitted raptors (Crocker-Bedford 1990).
LITERATURE CITED
AOU (American Ornithologists' Union). 1998. Check-List of North American Birds. Seventh Edition. American Ornithologists' Union, Washington, D.C. 829 pp.
Austin, K. K. 1993. Habitat use and home range size of breeding northern goshawks in the southern Cascades. M.S. thesis, Oregon State University, Corvallis.
Beier, P, and J.E. Drennan. 1997. Forest structure and prey abundance in foraging areas of northern goshawks. Ecological Applications 7(2):564-571.
Bent, A. C. 1937. Life histories of North American birds of prey. Part 1, U. S. National Museum Bulletin. 170. 482pp.
Bond, R. M. 1942. Development of young goshawks. Wilson Bull. 54:81-88.
Brown, L., and D. Amadon. 1968. Eagles, hawks and falcons of the world. 2 Vols. Country Life Books, London. 945pp.
Buchanan, J. B., L.L. Irwing, and E. L. McCutchen. Characteristics of spotted owl nest trees in the Wenatchee National Forest. Journal of Raptor Research, v.27, n.1, 1993:1-7.
Call, M. W. 1978. Nesting Habitats and surveying techniques for common western raptors. Technical Note TN-316. U.S. Department of the Interior - Bureau of Land Management, Denver Service Center.
Craighead, J. J., and F. C. Craighead, Jr. 1956. Hawks, owls and wildlife. Stackpole Books, Harrisburg, PA. 443pp.
Crocker-Bedford, D. C. 1990. Goshawk reproduction and forest management. Wildlife Society Bulletin 18: 262-269.
Gaines, D. 1988. Birds of Yosemite and the East Slope. Artemisia Press, Lee Vining California. 352 pp.
Garrett, K. and J. Dunn. 1981. Birds of Southern California: Status and Distribution. Los Angeles Audubon Society. 407 pp.
Grinnell, J. and A.H. Miller. 1944. The Distribution of the Birds of California. Pacific Coast Avifauna Number 27. Copper Ornithological Club, Berkeley, California. Reprinted by Artemisia Press, Lee Vining, California; April, 1986. 617 pp.
Hall, P.A. 1993. A comparison of nest sites of the northern goshawk in Arizona and California. J. Captor Research 27:72.
Hargis, C. D., C. McCarthy, and R. D. Perloff. 1994. Home ranges and habitats of northern goshawks in eastern California. Studies in Avian Biology 16: 66-74.
Harrison, C. 1978. A field guide to the nests, eggs and nestlings of North American birds. W. Collins Sons and Co., Cleveland, OH. 416pp.
Iverson, G.C., G. D. Hayward, K. Titus, E. De Gayner, R. E. Lowell, D. C. Crocker-Bedford, P.F. Schempf and J. Lindell. Conservation assessments for the northern goshawk in southeast Alaksa. U S Forest Service General Technical Report PNW, n. 387, 1996:I-IV, 1-101.
Jackman, S. M., and J. M. Scott. 1975. Literature review of twenty-three selected forest birds of the Pacific Northwest. U.S. Dep. Agric., For. Serv., Reg. 6, Portland OR. 382pp.
Jones, S. 1979. The accipiters - goshawk, Cooper's hawk, sharp-shinned hawk. U.S. Dept. Inter., Bur. Land Manage., Washington DC. Tech. Note TN-335. 51pp.
Kennedy, P. L. 1997. The northern goshawk (Accipiter gentilis atricapillus): Is there evidence of a population decline? J. Raptor Research 31: 95-106.
Lilieholm, R. J., W. B. Kessler, and K. Merrill. 1993. Stand density index applied to timber and goshawk habitat objectives in Douglas-fir. Environmental Management 17: 773-779.
Mallette, R. D., and G. I Gould, Jr. 1978. Raptors of California. Calif. Dept. Fish and Game, Sacramento. 58pp.
Patten, Michael . 1998. Pers. Comm. Riverside County Editor for American Field Notes and Past Secretary, California Bird Records Committee
Remsen, J. V. Jr. 1978. Bird Species of Special Concern in California. State of California. Department of Fish and Game. Supported by Federal Aid in Wildlife Restoration, Project Pr W-54-R-9, Nongame Wildlife Investigation, Wildlife Management Branch Administrative Report No. 78-1. 54 pp.
Reynolds, R. T., E. C. Meslow, and H. M. Wight. 1982. Nesting habitat of coexisting Accipiters in Oregon. J. Wildl. Manage. 46:124-138.
Schnell, J. H. 1958. Nesting behavior and food habits of goshawks in the Sierra Nevada of California. Condor 60:377-403.
Shipman, M. S. And M. J. Bechard. 1995. Post-fledgling movements and habitat use of northern goshawks (Accipiter gentilis) in the shrubsteppe habitat of northeastern Nevada. Abstract of Raptor Research Foundation annual meeting, Flagstaff, AZ.
Shuster, W. C. 1980. Northern goshawk nest site requirements in the Colorado Rockies. West. Birds 11:89-96.
Siders, M. S., and P. L. Kennedy. 1996. Forest structural characteristics of accipiter nesting habitat: Is there an allometric relationship? Condor 98: 123-132.
Squires, John R. and Richard T. Reynolds. 1997. Northern Goshawk (Accipter gentilis). In The Birds of North America, No. 298 (A. Poole and F. Gill, eds.) . The Academy of Natural Sciences, Philadelphia, PA and The American Ornithologists' Union, Washington D.C.
Squires, J. R., and L. F. Ruggiero. 1995. Winter movements of adult northern goshawks that nested in south-central Wyoming. Journal of Raptor Research 29: 5-9.
Squires, J. R., and L. F. Ruggiero. 1996. Nest site preference of northern goshawks in south-central Wyoming. J. Wildlife Management 60: 170-177.
Terres, J. K. 1980. The Audubon Society Encyclopedia of North American Birds. Alfred A. Knopf, New York, New York. 1109pp.
United States Forest Service (USFS). 1999. Pers. comm. Species accounts for threatened, endangered and sensitive wildlife species occurring in the San Bernardino National Forest.
Watson, J. W., D. W. Hays, S. P. Finn, and P. Meehan-Martin. 1998. Prey of breeding northern goshawks in Washington. J. Raptor Research 32: 297-305.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
Northern harrier (Circus cyaneus) - breeding
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
Northern harrier (Circus cyaneus) - breeding
Status:
State: Species of Special Concern
Federal: Partners in Flight Priority Bird Species
GROUP DESIGNATION AND RATIONALE
Group 3
The northern harrier occurs in a widely scattered distribution predominantly throughout the lowland and foothills Bioregions but may occur sparsely within suitable habitat in the mountain Bioregions and rarely as a wintering bird within the Desert Transition Bioregion within the Plan Area. Although there are a few known breeding locations (Mystic Lake/San Jacinto Wildlife Area, Lake Skinner area, Chino Hills, Lake Mathews-Estelle Mountain, Lake Elsinore grasslands/Collier Marsh, Vail Lake/Wilson Valley/east Temecula Creek, and Garner Valley), most of the recorded northern harrier occurrences are of wintering birds. This species has specific habitat requirements for breeding (primary habitats: cismontane alkali marsh, freshwater marsh, playas and vernal pools, and grassland) but uses a wider array of Habitat for foraging and wintering (secondary Habitats: agriculture land, Riversidean alluvial fan sage scrub, and coastal sage scrub). Although not documented within the CNDDB and UCR databases, the Prado Basin/Santa Ana River contains substantial amounts of suitable Habitat and seems a likely future or undocumented breeding location.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 50,020 acres of suitable primary breeding and foraging Habitat for the northern harrier including grasslands, freshwater marsh, playa and vernal pool, and cismontane alkali marsh.
Objective 2
Include within the MSHCP Conservation Area the known and historic breeding locations at 1) Mystic Lake/San Jacinto Wildlife Area (Existing Core H; 17,470 acres), 2) the Lake Skinner/ Diamond Valley Lake area (Existing Core C plus Proposed Extension of Existing Cores 5, 6, 7; 29,060 acres), 3) Chino Hills (Proposed Extension of Existing Core 1; 270 acres), 4) Lake Mathews-Estelle Mountain (Existing Core C plus Proposed Extension of Existing Core 2; 23,710 acres), 5) Lake Elsinore grasslands/Collier Marsh (Subunit 7 of Elsinore Area Plan; 1,810 acres), 6) Vail Lake/Wilson Valley/east Temecula Creek (Proposed Core 7; 50,000 acres), and 7) Garner Valley (represented by suitable Conserved Habitat within the San Jacinto Mountains Bioregion; 1,850 acres excluding 490 acres of range allotment). Include within the MSHCP Conservation Area an additional 17,560 acres of suitable breeding Habitat at Potrero (represented by Subunit 1 of The Pass Area Plan) and the Prado Basin/Santa Ana River.
Objective 3
Include within the MSHCP Conservation Area at least 104,140 acres of suitable secondary foraging and wintering Habitat including agriculture land, Riversidean alluvial fan sage scrub, and coastal sage scrub.
Objective 4
Include within the MSHCP Conservation Area and buffer from disturbance the known nesting locations at the localities listed in Objective 2. Buffering of the nest sites will include conservation of Habitat within a 250 meter radius around each of the nest site locations and may include a variety of Habitats.
Objective 5
Within the MSHCP Conservation Area, maintain (once every 5 years) the continued use of, and successful reproduction at 75 percent of the known nesting areas (including any nesting locations identified in the MSHCP Conservation Area in the future). Successful reproduction is defined as a nest which fledged at least one known young.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
The northern harrier uses a relatively wide variety of Habitats, including agriculture lands and grasslands, playa, alkali marsh, marshlands, coastal sage scrub, chaparral, and other scrub Habitat (Garrett and Dunn 1981). Because they will use a relatively wide variety of wetlands and uplands for various parts of their life history, a wide range of Habitats has been included for this analysis. For the purpose of the conservation analysis, the primary breeding Habitat for the northern harrier includes grasslands, freshwater marsh, playa and vernal pools, and cismontane alkali marsh Habitats within all Bioregions. Potential secondary foraging and wintering Habitat for the northern harrier includes agriculture land, Riversidean alluvial fan sage scrub, and coastal sage scrub in all Bioregions. Based on these Habitats, the Plan Area supports a total of approximately 685,010 acres of potential nesting and foraging Habitat for the northern harrier. The Plan Area includes a total of 130,280 acres of primary Habitat and 554,730 acres of secondary Habitat. Table 1 shows the conservation and loss of potential Habitat for the northern harrier. Overall, approximately 304,400 acres (45 percent) of potential Habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public Lands. Approximately 41,350 acres of primary Habitat (32 percent) will be conserved within the MSHCP Conservation Area and 263,050 acres (47 percent) of secondary Habitat will be conserved within the MSHCP Conservation Area.
The Riparian/Riverine Areas and Vernal Pools policy described in Section 6.1.2 of the MSHCP, Volume I, provides for conservation of wetlands which provide Habitat for this species through avoidance and minimization. Mitigation for impacts to wetlands shall be incorporated in accordance with the "No Net Loss" policy of federal and state wetland regulations. The proposed mitigation shall be directly related to the functions and values of the wetland as related to this species and result in equivalent replacement. This policy is extremely important to providing protection especially for the nesting Habitat and also for the Habitats that are used very frequently for foraging.
There are definable locations for focusing conservation efforts where the species is currently known to breed or has been documented to breed in the past. The core breeding areas include Mystic Lake/San Jacinto Wildlife Area (Existing Core H; 17,470 acres), the Lake Skinner/Diamond Valley Lake area (Existing Core C plus Proposed Extension of Existing Cores 5, 6, 7; 29,060 acres), Chino Hills (Proposed Extension of Existing Core 1; 270 acres), Lake Mathews-Estelle Mountain (Existing Core C plus Proposed Extension of Existing Core 2; 23,710 acres), Lake Elsinore
TABLE 1
SUMMARY OF HABITAT CONSERVATION
NORTHERN HARRIER
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| Primary Breeding Habitat in all Bioregions | |||||||
| Cismontane Alkali Marsh | 150 | 40 | 0 | 40 | 0 | 110 | 110 |
| Freshwater Marsh | 470 | 170 | 240 | 410 | 0 | 60 | 60 |
| Playas and Vernal Pools | 7,910 | 3,830 | 2,920 | 6,750 | 0 | 1,160 | 1,160 |
| Grassland | 146,870 | 20,010 | 22,810 | 42,820 | 12,220 | 91,830 | 104,050 |
| Subtotal Primary Breeding Habitat | 155,400 | 24,050 (15%) |
25,970 (17%) |
50,020 (32%) |
12,220 (8%) |
93,160 (60%) |
105,380 (68%) |
| Secondary Foraging or Wintering Habitat in all Bioregions | |||||||
| Agriculture Land (field crops) | 123,780 | 7,250 | 9,940 | 17,190 | 820 | 105,770 | 106,590 |
| Riversidean Alluvial Fan Sage Scrub | 7,150 | 3,170 | 2,060 | 5,230 | 220 | 1,700 | 1,920 |
| Coastal Sage Scrub | 152,690 | 47,160 | 34,560 | 81,720 | 26,240 | 44,730 | 70,970 |
| Subtotal Secondary Habitat | 283,620 | 57,580 (20%) |
46,560 (16%) |
104,140 (36%) |
27,280 (10%) |
152,200 (54%) |
179,480 (64%) |
| TOTAL | 439,020 | 81,630 (19%) |
72,530 (17%) |
154,160 (35%) |
39,500 (9%) |
245,360 (56%) |
284,860 (65%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
grasslands/Collier Marsh (Subunit 7 of Elsinore Area Plan; 1,810 acres), Vail Lake/Wilson Valley/ east Temecula Creek (Proposed Core 7; 50,000 acres), and Garner Valley (represented by suitable Conserved Habitat within the San Jacinto Mountains Bioregion; 1,850 acres of which 490 acres is within a range allotment). Although not documented as being present, the Prado Basin area and Potrero Valley area (17,560 acres) contain substantial amounts of suitable Habitat and seems a likely future or undocumented breeding locations. A total of 141,240 acres (not including that Habitat within the range allotment) of core breeding areas and likely or potential breeding areas are conserved within Criteria Area or Public/Quasi-Public designations. The core breeding areas are predominantly composed of freshwater marsh and playa and vernal pool Habitats with some grassland areas included. Areas adjacent to or within these core breeding areas, composed of the secondary Habitats, will be conserved. Thus, a large contiguous area within the known and recent Core Area at Mystic Lake/San Jacinto Wildlife Area will be conserved. Additionally, the core breeding areas at Lake Skinner, Chino Hills, Lake Mathews-Estelle Mountain, Lake Elsinore grasslands/Collier Marsh, and Vail Lake/Wilson Valley/east Temecula Creek, and Garner Valley will be conserved. This species has other potential Core Areas that are conserved within Criteria Area or Public/Quasi-Public designations including the Prado Basin and Potrero Valley which contain substantial amounts of suitable Habitat. As described below under Data Characterization, 62 of the 148 recent point localities have a high location precision. Of these 62 point localities, 26 will be inside the Criteria Area or Public/Quasi-Public Lands. A total of 36 point localities will be outside of the MSHCP Conservation Area, 10 of which are recorded for developed areas.
As a Group 3 species the conservation of the northern harrier requires species specific conservation measures. Northern harriers have been identified to incur breeding losses by agriculture operations and other activities that disturb nesting areas during the nesting season. Conservation measures include the implementation of Objective 4 which will include within the MSHCP Conservation Area and buffer from disturbance the known nesting locations within the core breeding areas listed above. Buffering of the nest sites will include conservation of Habitat within a 250 meter radius around each of the nest site locations and may include a variety of Habitats. The MSHCP Conservation Area also will maintain (once every 5 years) the continued use of, and successful reproduction at 75 percent of the known nesting areas (including any nesting locations identified in the MSHCP Conservation Area in the future). Successful reproduction is defined as a nest which fledged at least one known young.
MSHCP Conservation Area Configuration Issues
Several large blocks of Habitat including foraging and nesting locations of the northern harrier will be conserved as Criteria Area and Public/Quasi-Public designations, including the Chino Hills area, Prado Basin/Santa Ana River, Lake Mathews-Estelle Mountain, Lake Elsinore grassland and Collier Marsh, Wasson Canyon, Santa Rosa Plateau Nature Reserve, Hogbacks, Lake Skinner/Diamond Valley Lake, Mystic Lake/San Jacinto Wildlife Area, Badlands, Vail Lake/Wilson Valley, Potrero, and grasslands within the San Bernardino and Cleveland National Forest especially the Garner Valley area. Smaller areas of conservation are provided in the Temecula/Murrieta Hot springs area within the AD161 mitigation area. They have also been observed in smaller numbers at a variety of other areas that will be conserved including Motte-Rimrock Reserve, Sedco Hills, Sycamore Canyon Regional Park, and vernal pools west of Hemet. These locations are likely wintering birds and not nesting locations although if suitable nesting conditions are present the northern harrier could nest in these areas as well.
As identified above, the species occurs within the MSHCP Plan Area predominantly as a transient, migrant, or wintering species. As such, the MSHCP Conservation Area will provide adequate Habitat for foraging during these visits to the area as well as Habitat containing potential nest conditions with adequate protection around each nest site and foraging areas during the breeding season. The nesting locations are the focus of this MSHCP Plan. These MSHCP Conservation Area locations are interconnected as well, though the ability of this species to move long distances may reduce the importance of these linkages for this species.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 50,020 acres of suitable primary Conserved Habitat and 104,140 acres of suitable secondary Conserved Habitat and 7 Core Areas and 2 potential Core Areas within large blocks of Habitat in the MSHCP Conservation Area. The MSHCP Conservation Area will maintain (once every 5 years) the continued use of, and successful reproduction at 75 percent of the known nesting areas (including any nesting locations identified in the MSHCP Conservation Area in the future) and will conserve within the MSHCP Conservation Area and buffer from disturbance the known nesting locations within the core breeding areas listed above. Buffering of the nest sites will include conservation of Habitat within a 250 meter radius around each of the nest site locations and may include a variety of Habitats. The current population size of the northern harrier is unknown and most locations are observations of wintering/migrating birds. However, historic breeding locations occur within the Mystic Lake/San Jacinto Wildlife Area, Lake Skinner, Lake Elsinore grassland/Collier Marsh, Lake Mathews-Estelle Mountain, Chino Hills, and Vail Lake/Wilson Valley/eastern Temecula Creek, and Garner Valley areas which are within conserved areas.
INCIDENTAL TAKE
The Incidental Take of the northern harrier is difficult to quantify at this time owing to our limited knowledge of the precise location and extent of nesting sites and the fact that losses may be masked by fluctuations in abundance and distribution during the life of the permit. However, the level of Take of the northern harrier can be anticipated by the loss of the number of acres of Habitat that will become unsuitable for this species.
About 284,860 acres (65 percent) of potential Habitat for the northern harrier will be outside the Criteria Area and Public/Quasi-Public designations, and individuals within this Habitat will be subject to Incidental Take consistent with the Plan. Of the primary Habitats, 105,380 acres will be outside the MSHCP Conservation Area, or about 68 percent of the potential primary Habitat, most of which is grassland Habitat. Of the secondary Habitats, about 179,480 acres will be outside the MSHCP Conservation Area, or about 63 percent of the potential secondary Habitats, most of which is agriculture Habitat. It should also be noted that wetland Habitats located outside the MSHCP Conservation Area will be subject to the Protection of Species Associated with Riparian/Riverine Areas and Vernal Pools policy presented in Section 6.1.2 of the MSHCP, Volume I. Based on recent breeding location information, a breeding location is recorded for Garner Valley. A total of 490 acres of this Core breeding Area is located within the Garner Range Allotment and is considered to not be conserved although it is within the San Bernardino National Forest. No Take of active nest sites will be permitted. A total of 36 point localities will be outside of the MSHCP Conservation Area, 10 of which are recorded for developed areas.
Other areas not conserved where the northern harrier has been documented to occur but that have not been documented for breeding locations include parts of the Temecula/Murrieta Hot Springs area, San Jacinto, Moreno Valley, Hemet, Santa Rosa Plateau outside of the Santa Rosa Plateau Nature Reserve, and Beaumont.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The location database for the northern harrier includes approximately 202 data records from 1887 to 1999. Of these records, approximately 148 are dated within the past 10 years and 62 are of high precision and may be accurately located within the Plan Area. Approximately 10 of these high precision records are located within developed areas and likely no longer exist. The rest occur within non-native grassland, sage scrub, chaparral, croplands, alkali playa and marshland, as well as other vegetation communities that are likely occupied by the species for foraging or nesting. Most of the records are likely to be for wintering birds due to the migratory habits of the species (Garrett and Dunn1981). The UCR database does not identify those records that are breeding locations. Other sources provided documentation of nesting of the northern harrier within the Plan Area (Cooper 2001).
A moderate amount of literature is available for the northern harrier because it is a bird of prey and due to its ease of detection and observation. Most of the literature pertains to general natural history and the harriers in general. Few controlled scientific studies have been conducted, however some management studies are available. Very little information is available for the Plan Area other than what is available regarding basic distribution information.
Habitat and Habitat Associations
The northern harrier frequents open wetlands, wet and lightly grazed pastures, old fields, dry uplands, upland prairies, mesic grasslands, drained marshlands, croplands, shrub-steppe, meadows, grasslands, open rangelands, desert sinks, fresh and saltwater emergent wetlands and is seldom found in wooded areas (Bent 1937; MacWhirter and Bildstein 1996). It uses tall grasses and forbs in wetlands, or at wetland/field borders for cover; it roosts on the ground (Bent 1937). No data was found on water requirements, but it frequents aquatic Habitats. The home range usually includes fresh water. It is mostly found in flat, or hummocky, open areas of tall, dense grasses, moist or dry shrubs, and edges for nesting, cover, and feeding (Bent 1937). While it seems to prefer to nest in the vicinity of marshes, rivers, or ponds, it may be found nesting in grassy valleys or on grass and sagebrush flats many miles from the nearest water (Call 1978). In a shrub-steppe Habitat, the northern harrier was determined to use riparian and cultivated Habitats disproportionately (Martin 1987). In general, it prefers saltwater marshes, wet meadows, sloughs, and bogs for its nesting and foraging Habitat and if these are absent, it hunts open fields and is frequently observed hunting over agricultural areas (Call 1978). The California population has decreased in recent decades (Grinnell and Miller 1944, Remsen 1978), but can be locally abundant where suitable Habitat remains free of disturbance, especially from intensive agriculture. In both wetland and upland areas, the densest populations typically are associated with large tracts of undisturbed Habitats dominated by thick vegetative growth (MacWhirter and Bildstein 1996).
Biogeography
The northern harrier occurs as a breeding bird across the northern United States and Canada, throughout most of California and the central portion of the United States south to Texas. It is absent from desert regions as a breeding bird and the southeastern parts of the United States (Bildstein 1988). Specifically, it occurs as a breeding bird from northern Alaska and Canada south to the northern Baja Peninsula east to southern Nevada, southern Utah, northern New Mexico, northern Texas, southern Kansas, central Iowa, central Wisconsin, southern Michigan, northern Ohio, southern Pennsylvania, southeastern Virginia and probably in northeastern North Carolina (MacWhirter and Bildstein 1996). It appears to be most numerous in the northern great plains from the Dakotas and Montana into southern Canada (Bildstein 1988). During the winter, the northern harrier occurs throughout southern Canada and all of the United States (Bildstein 1988). The usual southern limit for wintering is Panama (MacWhirter and Bildstein 1996).
In California, the northern harrier occurs from annual grassland up to lodgepole pine and alpine meadow Habitats, as high as 3,000 meters (10,000 feet) (Garrett and Dunn 1981). It breeds from sea level to 1,700 meters (0-5,700 feet) in the Central Valley and Sierra Nevada, and up to 800 meters (3,600 feet) in northeastern California. It is a permanent resident of the northeastern plateau and coastal areas; it is a less common resident of the Central Valley. It is a widespread winter resident and migrant in suitable Habitat. Some individuals migrate into California; others migrate through to Central America or northern South America (Garrett and Dunn 1981).
Known Populations Within Western Riverside County
The northern harrier is widespread throughout the Plan Area but is absent from the forested areas of Cleveland National Forest and the San Bernardino National Forest. Although not documented within the database, it may occur within the grassland areas of the national forests (Garrett and Dunn 1981). It occurs predominantly within the Riverside Lowlands and San Jacinto Foothills but also occurs in the chaparral dominated areas of the Santa Ana Mountains Bioregions and sparsely within the San Jacinto Mountains. It is well distributed within the Riverside Lowlands Bioregions in a variety of Habitats. It is considered a common winter resident throughout the Plan Area. Breeding locations are not documented within the UCR database but it has been documented as a scarce and local breeding bird in the literature (Garrett and Dunn 1981). A recent review of avian use of the Plan Area indicates breeding locations of the northern harrier at Mystic Lake/San Jacinto Wildlife Area (Garrett and Dunn 1981), 1 to 3 nesting territories in the Lake Skinner area (P. Bloom 2002 pers. comm.), Chino Hills, Lake Mathews-Estelle Mountain, Lake Elsinore grassland/Collier Marsh, Vail Lake/Wilson Valley/east Temecula Creek, and Garner Valley (Cooper 2001). These breeding locations will be considered the Core Areas for the species.
Biology
Genetics: No information is available in the literature.
Diet and Foraging: The northern harrier feeds mostly on small and medium sized mammals, primarily rodents, birds, frogs, small reptiles, crustaceans, insects, and, rarely on fish (Terres 1980). In the winter in the northern part of its range, it takes almost exclusively Microtus whereas in the southern part, mammals and birds are taken (MacWhirter and Bildstein 1996). It makes low, quartering flights 1-9 meters (3-30 feet) above open ground. It dives from a flight or a hover; it rarely perches and pounces on prey (Zeiner et al. 1990). Areas of short vegetation such as heavily grazed pasture and harvested fields, are under used, whereas idle and abandoned fields with vegetative cover are used more than expected (Bildstein 1988).
Daily Activity: The northern harrier exhibits year-long, diurnal activity (Zeiner et al. 1990).
Reproduction: The northern harrier nests on the ground in shrubby vegetation or patches of dense vegetation, usually at the marsh edge (Brown and Amadon 1968; Toland 1987). The northern harrier mostly nests in emergent wetland or along rivers or lakes, but may nest in grasslands, grain fields, or on sagebrush flats several miles from water (Call 1978). The northern harrier is very eclectic in its choice of vegetative cover, even within a single area. In a continent wide sample, 17 percent of nests were in wet marsh meadows dominated by willow, grasses, sedges, and herbaceous shrubs; 18 percent were in freshwater marshes dominated by tall grasses, reeds, bulrushes, and cattails; 26 percent were in dry grasslands including bromegrass and wheatgrass; 8 percent were in cultivated fields such as alfalfa and rangeland prairies (MacWhirter and Bildstein 1996). The nest is a relatively flimsy structure built of a large mound of sticks, straws, or grasses on wet areas, and a smaller cup of grasses on dry sites (Call 1978). Nests were placed an average of 3.5 meters from the outer edge of each patch of dense vegetation (Toland 1987).
It breeds in April to September, with a peak of activity in June through July. It is single-brooded; the clutch averages 5 eggs, with a range from 3-12 eggs (Harrison 1978). The female incubates while the male provides food. The nesting period lasts about 53 days (Craighead and Craighead 1956). Breeding pairs and juveniles may roost communally in late autumn and winter (Smith and Murphy 1973).
Survival: In Idaho, hatching success of the northern harrier was 69.6 percent, fledging success was 60 percent of the eggs that hatched and an average of 3.3 young fledged per successful nest (Toland 1987). The annual reproductive success of all nests averaged 1.8 offspring fledged per pair (MacWhirter and Bildstein 1996). Among 114 banded birds, the mean age at death was 16.6 months with the longest life span reported as 16 years 5 months (MacWhirter and Bildstein 1996; Bildstein 1988). The pre-1950s mortality rates have been estimated as 59 percent in the first year and 30 percent among adults (Bildstein 1988).
Dispersal: There appears to be virtually no fidelity by the offspring of the northern harrier to their natal area (MacWhirter and Bildstein 1996).
Socio-Spatial Behavior: The following home range and travel distance for the northern harrier is summarized by Craighead and Craighead (1956). In Utah, 5 breeding home ranges averaged 429 hectares (1,060 acres), and varied from 363-518 hectares (896-1,280 acres). In Michigan, individuals flew 1.6 to 8.8 km (1 to 5.5 miles) daily from a communal roost to foraging areas. Daily foraging areas varied from 12-16 hectares (30-40 acres) to 259 hectares (640 acres). Also in Michigan, 15 breeding home ranges averaged 405 hectares (1,000 acres), and varied from 98-770 hectares (243-1,920 acres).
In Wisconsin, the breeding home range of 1 radio-tagged pair of northern harriers included an area 2 x 4.4 kilometers (1.25 x 2.75 miles), or 890 hectares (2,200 acres) (Hamerstrom and Wilde 1973). In Manitoba, the territory extended 28 hectares (96 acres) around nests (Hecht 1951). In Idaho, mean home ranges of males were estimated at 15.7 square kilometers while those of females were estimated at 1.13 square kilometers and males ranged up to distances of 9.5 kilometers from the nest (Martin 1987). Apparently the northern harrier is not territorial during the winter and may forage and roost communally (Bosakowski and Smith 1996).
Community Relationships: The northern harrier is very defensive of its territory; it will attack other, more formidable birds of prey, and humans during the breeding season (Zeiner et al. 1990). The northern harrier competes with buteos, especially red-tailed and red-shouldered hawks, for food. It is often considered a diurnal counterpart of the short-eared owl (Terres 1980).
Threats to Species
The breeding population of the northern harrier is much reduced, especially in the southern coastal district (Zeiner et al. 1990). The destruction of wetland Habitat, native grassland, and moist meadows, and burning and plowing of nesting areas during early stages of the breeding cycle, are major reasons for the decline (Remsen 1978). MacWhirter and Bildstein (1996) summarize the threats as follows. The continued widespread destruction of freshwater and estuarine wetlands in the United States poses a threat to the breeding and wintering populations. Conversion of native grassland prairies for monotypic farming has contributed to local population declines. In upland areas, mechanized agriculture and early mowing have increased the threat of nest destruction. Overgrazing of pastures, and the advent of larger crop fields and fewer fence rows, together with the widespread use of insecticides and rodenticides, have reduced prey availability and thus the amount of appropriate Habitat for the species.
During the late 1960s and early 1970s, levels of DDT in some eggs were high enough to cause eggshell thinning but after that time show no elevated levels and population declines may be attributed to a number of other factors, including loss of suitable Habitat (Noble and Elliott 1990).
Special Biological Considerations
Population estimates and estimates of reproductive success may be difficult to make for the northern harrier. This is due to its ground-nesting behavior which makes it difficult to census. Additionally, the harrier tends to not flush from the nest until the observer is within 2 meters of the nest (Lehman et al. 1998).
The population size may increase with some agricultural practices (e.g., grain crops), provided that cover and nesting Habitat is preserved or enhanced. The population may also increase in response to the prey population size due to nomadic movements from one area to another (MacWhirter and Bildstein 1996). Nesting success was higher in pairs nesting in idled sections of a park in Idaho than in managed sections (Toland 1987). Nest site selection may be a compromise between the availability of a wet nest site, the close proximity to optimum foraging Habitat, and access to a mate with a high food provisioning rate (Simmons and Smith 1985). Locally, the nesting numbers and reproductive success are affected by prey availability, predation, nest-site quality, and weather (MacWhirter and Bildstein 1996).
In comparative studies of nesting use of managed versus non-managed grasslands, northern harriers were found to locate their nests in fields not disturbed by recent management activities (within the previous 12 months) (Herkert, et al. 1999). Overall, northern harrier nest placement was not influenced by whether fields were dominated by native or nonnative grasses (Herkert, et al. 1999). Relative abundance of nesting pairs of harriers was not significantly different inside versus outside a military training area and nesting success of the species showed no difference based on location relative to the military training area (Lehman, et al. 1999).
Northern harriers have been observed to establish communal roosts and contain from 21 to 43 individuals and are only observed in undisturbed cool-season grasses (Walk 1998).
Wetland preservation for waterfowl and Habitat management practices for upland game birds are beneficial. Management recommendations include the protection of undisturbed Habitat in which annual vegetation and successional plants can grow and dead vegetation is not removed. Timing of harvest and activities within nesting areas may avoid destroying active nests of the northern harrier. In other areas, there is recommended active maintenance of old fields and shrubby Habitats through prescribed burning and grazing to prevent reforestation. Also, in other areas, it has been recommended to eliminate winter livestock grazing from wetland and grassland ecosystems to improve the winter Habitat (MacWhirter and Bildstein 1996).
LITERATURE CITED
Bent, A. C. 1937. Life histories of North American birds of prey. Part 1. U.S. Natl. Mus. Bull. 167. 409pp.
Bildstein, K. L. 1988. Northern Harrier. Pp. 251-303 in R. S. Parmer, ed. Handbook of North American birds. Vol. 4: diurnal raptors, part 1. Yale Univ. Press, New Haven, CT.
Bloom, P. 2002. Pers.comm.
Bosakowski, T., and D. G. Smith. 1996. Group hunting forays of wintering northern harriers, Circus cyaneus: An adaptation of juveniles? Canadian Field-Naturalist 110: 310-313.
Brown, L., and D. Amadon. 1968. Eagles, hawks and falcons of the world. 2 Vols. Country Life Books, London. 945pp.
Call, M. W. 1978. Nesting habits and survey techniques for common western raptors. U. S. Dep. Inter., Bur. Land Manage., Portland, OR. Tech. Note No. 316. 115pp.
Cooper, D. S. 2001. California Important Breeding Areas. Audubon California. Los Angeles.
Craighead, J. J., and F. C. Craighead, Jr. 1956. Hawks, owls and wildlife. Stackpole Books, Harrisburg, PA. 443pp.
Garrett, K., and J. Dunn. 1981. Birds of southern California. Los Angeles Audubon Soc. 408pp.
Grinnell, J., and A. H. Miller. 1944. The distribution of the birds of California. Pac. Coast Avifauna No. 27. 608pp.
Hamerstrom, F., and D. R. Wilde. 1973. Cruising range and roosts of an adult harrier. Island Bird Banding News 45:123-127.
Hecht, W. R. 1951. Nesting of the marsh hawk at Delta, Manitoba. Wilson Bull. 63:167-176.
Harrison, C. 1978. A field guide to the nests, eggs and nestlings of north American birds. W. Collins Sons and Co., Cleveland, OH. 416pp.
Herkert, J. R., S. A. Simpson, R. L. Westemeier, T. L. Esker, and J. W. Walk. 1999. Response of northern harriers and short-eared owls to grassland management in Illinois. Journal of Wildlife Management 63: 517-523.
Lehman, R.N., L.B. Carpenter, K. Steenhof, and M.N. Kochert. 1998. Assessing relative abundance and reproductive success of shrubsteppe raptors. J. Field Ornithology 69:244-256.
Lehman, R. N., K. Steenhof, M. N. Kochert, and L. B. Carpenter. 1999. Effects of military training activities on shrub-steppe raptors in southwestern Idaho. Environmental Management 23: 409-417.
MacWhirter, R. B., and K. L. Bildstein. 1996. Northern Harrier (Circus cyaneus). In The Birds of North America, No. 210 (A. Poole and F. Gill, eds.). The Academy of Natural Sciences, Philadelphia, and The American Ornithologists' Union, Washington, D.C.
Martin, J. W. 1987. Behavior and Habitat use of breeding northern harriers in southwestern Idaho. Journal of Raptor Research 21: 57-66.
Noble, D. G., and J. E. Elliott. 1990. Levels of contaminants in Canadian raptors, 1966 to 1988: Effects and temporal trends. Canadian Field-Naturalist 104: 222-243.
Remsen, J. V., Jr. 1978. Bird species of special concern in California. Calif. Dep. Fish and Game, Sacramento. Wildl. Manage. Admin. Rep. No. 78-1. 54pp.
Simmons, R., and P. C. Smith. 1985. Do northern harriers (Circus cyaneus) choose nest sites adaptively? Canadian Journal of Zoology 63: 494-498.
Smith, D. G., and J. R. Murphy. 1973. Breeding ecology of raptors in the eastern Great Basin of Utah. Brigham Young Univ., Provo. Sci. Bull. Biol. Ser. 18, No. 3. 76pp.
Terres, J. K. 1980. The Audubon Society encyclopedia of North American birds. A. Knopf, New York. 1100pp.
Toland, B. R. 1987. Nesting ecology of northern harriers in southwest Missouri. Transactions of the Missouri Academy of Science 20: 49-58.
Walk, J. W. 1998. Winter roost sites of northern harriers and short-eared owls on Illinois grasslands. Journal of Raptor Research 32: 116-119.
Zeiner, D.C., W. F. Laudenslayer, K. E. Mayer and M. White eds. 1990. California's Wildlife: Volume II - Birds. California Department of Fish and Game. Sacramento, California. 732 pp.
osprey (Pandion haliaetus)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
osprey (Pandion haliaetus)
Status:
State: Species of Special Concern; California Department of Forestry and Fire Prevention Sensitive
Federal: Partners in Flight Priority Bird Species; San Bernardino National Forest Sensitive
Other: Audubon Society Local Concern
GROUP DESIGNATION AND RATIONALE
Group 2
The osprey is relatively widely distributed throughout the MSHCP Plan Area within suitable Habitat. It occurs at almost every open water body within the Plan Area. There are several areas that appear to be Core Areas including the Santa Ana River, Lake Mathews, Lake Elsinore, Canyon Lake, Vail Lake, Lake Skinner, Lake Perris, Mystic Lake, and Lake Hemet. Although it has not been documented to nest within the Plan Area, there is suitable Habitat for nesting and nesting locations will be important to conserve.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 10,340 acres of open water Habitat at the following seven locations: Lake Mathews, Diamond Valley Lake, Lake Skinner, Lake Elsinore, Vail Lake, Lake Perris, and Mystic Lake/San Jacinto Wildlife Area.
Objective 2
Include within the MSHCP Conservation Area at least 5,520 acres of suitable riparian and open water Habitat within the Prado Basin and Santa Ana River.
Objective 3
A 100-meter buffer will be established around open water bodies identified in Objective 1 as they are incorporated into the MSHCP Conservation Area.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
For the purpose of the conservation analysis, potential Habitat for the osprey includes open water lakes and reservoirs, a shoreline buffer of 100 meters around each of the open water lakes and reservoirs (to be established as these areas are incorporated into the MSHCP Conservation Area), and the riparian Habitat and open water within the Prado Basin/Santa Ana River. Although the osprey has not been documented to nest within the MSHCP Plan Area, potential Habitat and previous nesting attempts occur at Lake Elsinore. Vail Lake and Lake Skinner appear to be likely areas where the osprey may attempt to breed. Based on these Habitats, the Plan Area supports approximately 18,000 acres of potential Habitat for the osprey. Table 1 shows the conservation and loss of potential Habitat for the osprey. Overall, approximately 15,860 acres (88 percent) of potential Habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public Lands.
As described below under Data Characterization, 11 of the 17 recent point localities have a high location precision. Of these 11 point localities, 6 will be inside the Criteria Area or Public/Quasi-Public lands. However, of the five points located outside these Habitat areas, all are mapped in existing residential/urban/exotic areas or in existing agriculture or other upland Habitats. These Habitats do not constitute suitable Habitat but these locations may have been of a bird flying overhead or within Habitat adjacent to one of the reservoirs where they might hunt. Conservation of this species will be considered from a landscape perspective because the species is found throughout the Plan Area and is well documented for the type of Habitat within which they forage. Additionally there are definable locations for focusing conservation efforts that may constitute Core Areas and contain potential nesting areas. Any nesting locations, if they were to be identified, will be important to preserve.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
OSPREY
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP ConservationArea | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| All Bioregions | |||||||
| Open Water | 12,210 | 1,190 | 9,150 | 10,340 | 40 | 1,830 | 1,870 |
| Riparian Habitat within Prado Basin/Santa Ana River | 5,790 | 510 | 5,010 | 5,520 | 0 | 270 | 270 |
| TOTAL | 18,000 | 1,700 (9%) |
14,160 (79%) |
15,860 (88%) |
40 (<1%) |
2,100 (12%) |
2,140 (12%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
Currently there are no documented core breeding areas. Core areas for foraging or potentially for breeding that are conserved within the MSHCP Conservation Area include Lake Mathews, Diamond Valley Lake, Lake Skinner, Lake Elsinore, Vail lake, Lake Perris, Mystic Lake/San Jacinto Wildlife Area, and Prado Basin/ Santa Ana River. All of these locations may also contain potential Habitat for breeding. The 100-meter buffer to be established around each area as it is incorporated into the MSHCP Conservation Area will protect potential nesting areas.
MSHCP Conservation Area Configuration Issues
Several large blocks of Habitat supporting the current known locations and potential foraging and nesting locations of the osprey will be conserved as Criteria Area and Public/Quasi-Public lands, including the Prado Basin/Santa Ana River, Lake Skinner, Diamond Valley Lake, Lake Mathews, Mystic Lake/San Jacinto Wildlife Area, Lake Elsinore, and Vail Lake. As identified below, the dispersal distance for the species will allow them to cover the MSHCP Plan Area and they will be capable of dispersing from a nest site within the MSHCP Plan Area to any other part of the area. As such, the MSHCP Conservation Area will provide adequate Habitat for foraging during nomadic visits to the area and migratory stopovers as well as Habitat containing potential nest sites with adequate protection around each nest site and foraging areas during the breeding season. Foraging areas are provided at Vail Lake, Lake Skinner, Diamond Valley Lake area, Mystic Lake/San Jacinto Wildlife Area, Lake Elsinore, Lake Mathews, and Prado Basin/ Santa Ana River. Potential nest sites are provided at these areas in the form of a large trees or snags that may be used. These locations within the MSHCP Conservation Area are linked as well, however the osprey, due to its ability to move long distances, may rely less on the linkage than other species.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 15,860 acres of suitable Conserved Habitat, including open water and riparian Habitat in the Prado Basin/Santa Ana River, and the establishment of a 100-meter buffer around the open water bodies as they are incorporated into the MSHCP Conservation Area. The current population size of the osprey is unknown, and it has not been confirmed as to whether or not it is a breeding bird in the MSHCP Plan Area.
INCIDENTAL TAKE
About 2,140 acres (12 percent) of potential Habitat for the osprey will be outside the Criteria Area and Public/Quasi-Public designations and individuals in this Habitat will be subject to Incidental Take consistent with the Plan. Potential Core population Areas not included within the MSHCP Conservation Area include Canyon Lake and Lake Hemet. No Take of active nest sites will be permitted.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The location database for the osprey includes approximately 38 records dating from 1900 to 1999. The more recent records, a total of 25, dated from 1990 to present, include 11 records that have a high precision and can be accurately located within the western Riverside County Plan Area. Of these recent and high precision records, the locations are associated with non-native grassland, alkali playa, open water, Jeffrey pine, and sage scrub. The record locations for Habitats other than open water may reflect an observation of the osprey flying overhead or perched within a tree or forested area adjacent to water. The database does not include nesting information and nesting locations have not been confirmed. Most or all of the records may reflect nomadic movements of the species within the Plan Area.
The birds of prey, in general, have been studied more than most other avian groups and more ornithological literature is available for the group. The osprey, as a bird of prey, has a moderate amount of literature available but little information is available for the Plan Area.
Habitat and Habitat Associations
The osprey is restricted to large water bodies supporting fish with surrounding or nearby forest Habitats, often ponderosa pine or mixed conifer (Zeiner et al. 1990). Osprey often use rivers, lakes, and reservoirs for foraging and rocky pinnacles, and large trees and snags in open forest for cover and nesting (Zeiner et al. 1990; Call 1978). Ospreys historically bred throughout much of the continent in tall trees near productive shallow-water freshwater bodies. Ospreys need exposed locations to build their large nests, often in dead tops of older trees or snags in beaver swamps (Ewins 1997). If nesting sites are in short supply, they may nest a mile or more from water if the food supply proves adequate (Call 1978). Wintering Habitat is found along the California coast south of San Francisco (Zeiner et al. 1990).
Biogeography
The osprey is found on every continent except Antarctica (Terres 1980). Within North America it extends from northwestern Alaska to Baja California, Mexico and Florida (Terres 1980). Wintering Habitat begins in southern United States south to Peru and Brazil (Terres 1980). Within California, breeding populations reside in the Cascade and Sierra mountain ranges (Zeiner et al. 1990). Although widely seen on the coast, these birds are rare transients in the interior portions of southern California (Garrett and Dunn (1981). Ospreys are found in San Diego County between mid September and November (Unitt 1984).
The current literature documents that the closest breeding location of the osprey is in the southern portion of the Sierra Mountains and in Baja California. Although the numbers of pairs of the osprey have increased at the southern end of their range, the breeding range has not extended any farther south (Henny and Anthony 1989). Observations within San Diego County confirmed that an Osprey pair successfully nested in the Scripps Ranch area in 2001 (Brock Ortega 2001, pers. comm.).
Migration rates and locations were studied and the results indicate that western populations winter farther north and west of other populations in Mexico and Central America. They were observed to migrate 2 to 3 times faster in spring than in fall (Poole and Agler 1987).
Known Populations with Western Riverside County
Within Riverside county, the osprey occurs west of the San Jacinto Mountains and in other parts of Riverside County, it occurs at the Salton Sea but is also known to migrate through the San Gorgonio Pass and Coachella Valley (Zeiner et al. 1990; Miller and Stebbins 1964). It is an uncommon winter visitor along the coast of California including the western Riverside County area. It is most often encountered in fall and winter, although a few birds regularly remain through the summer, but is not documented as a breeding bird within the literature, thus it is considered a rare transient visitor of water bodies within the lowland and montane regions (Garrett and Dunn 1981).
The water bodies that have been recorded as being visited by the osprey include Santa Ana River, Prado Basin, Lake Mathews, Lake Elsinore, Canyon Lake, Lake Skinner, Lake Perris, San Jacinto Reservoir, Hemet Lake, and Mystic Lake/San Jacinto Wildlife Area. Other observations not associated with a water body may reflect an observation of the osprey flying overhead. Breeding attempts are apparently have been made at Lake Elsinore (K. Cleary-Rose 2002, pers. comm.).
Biology
Genetics: Based on DNA-DNA hybridization, studies support retaining the osprey as a subfamily separate from accipitrid raptors. The divergence between Pandionidae and Accipitridae is estimated to have occurred 24-30 million years ago (Seibold and Helbig 1995).
Diet and Foraging: Osprey often use rivers, lakes, and reservoirs for foraging for fish (Zeiner, et al. 1990). Ospreys prey mostly on fish but also take a few mammals, birds, reptiles and amphibians as well as invertebrates (Zeiner, et al. 1990). Mammals and birds may constitute important food sources at times and have been documented to make up 7.5 and 5.0 percent of the diet respectively (Chubbs and Trimper 1998).
Osprey spend much of their time near the water perched on a dead snag of a tree or on rocks, they fly out occasionally over the water surface to hunt; they fly about 30-100 feet above the surface; when they sight a fish, they hover with wings beating, legs trailing and sometimes plunge into the water from a straight flight. Upon capturing prey, they rise from the water with the fish gripped in both feet and fly to a habitual perch to eat the prey item (Terres 1980).
Daily Activity: The osprey is a year-long diurnally active species (Zeiner, et al. 1990).
Reproduction: Osprey often use rivers, lakes, reservoirs with large trees and snags in open forest for cover and nesting (Zeiner, et al. 1990). Osprey nest in trees or artificial platforms, on rocky or dirt pinnacles, in the tops of dead snags, or in the tops of live trees (Tishechkin and Ivanovsky 1992; Houston and Scott 1992; Call 1978). The osprey prefers to build the nest near accessory perches - they will utilize almost any elevated structure as a perch for sunning and protection from wind provided it remains within sight of the nest (Call 1978). They may nest in colonies or singly (Terres 1980). The same nest site is normally used year after year or as long as the tree remains standing (Call 1978). Nesting materials consist of large sticks, driftwood, and grasses or bark (Call 1978). Nests are most often constructed in the tops of conifers, but deciduous trees may also be used (Call 1978).
Osprey pairs average 59 successful copulations per clutch starting 14 days before and peaking in the few days before the start of egg laying. This supports the idea that in species with substantial paternal investment, males should also invest heavily in paternity assurance (Birkhead and Lessells 1988). The osprey breeds from March to September with a clutch size of 1 to 4 eggs, usually 3 eggs (Zeiner, et al. 1990). The mean clutch size has been estimated at 2.82 eggs and the mean size of successful broods is 2.06 (Tishechkin and Ivanovsky 1992). Incubation may last for 38 to 43 days although the incubation period has been reported to range from 28 to 43 days depending on the location and investigator (Terres 1980). Addled eggs and fallen nests were the main reason for reduced productivity (Tishechkin and Ivanovsky 1992). Early clutches produced more young in the successful nests (Tishechkin and Ivanovsky 1992 ).
Survival: Productivity surveys of osprey estimated an average productivity of 1.21 fledglings per occupied territory, 1.33 fledglings per breeding attempt and 2.04 fledglings per successful breeding attempt (Witt 1996). Ospreys are relatively long-lived with banding records for survival ranging from 18 to 32 years of age (Terres 1980).
Dispersal: A general increase in the nesting distribution and abundance of ospreys has occurred within the United States, however there has been limited dispersal into states with low or extirpated populations (Houghton and Rymon 1997). Young ospreys have been documented to return to the natal area when two years old or in the 3rd year but do not breed until three years old (Terres 1980).
Socio-Spatial Behavior: The home range for osprey extends up to 5-6 miles from the nest (Zeiner et al. 1990). The adults are fiercely defensive of the nest site (Terres 1980).
Community Relationships: The osprey competes with other raptors including bald eagles and gulls. Flath (1972) observed competition for nest sites with Canadian geese, even though nesting for the two species occurs at different times of year.
Threats to Species
Studies and review by Ewins (1997) provides a summary of past and current threats to the osprey as follows. Ospreys historically bred throughout much of the continent in tall trees near productive shallow-water freshwater bodies. Historical nest sites are poorly documented, but timber extraction and shoreline development have undoubtedly removed many preferred nest trees, likely causing population declines. Widespread use of persistent organochlorine pesticides after 1945 caused dramatic declines of breeding ospreys.
Osprey numbers appear to have declined starting in the early 1900s, probably due in large part to indiscriminate shooting (Kenyon 1947).
The species is susceptible to pollution within occupied waters which is believed may result in unsuccessful reproduction (Terres 1980). Due to their predatory Habitat and largely piscivorous diet, osprey are exposed to biomagnification hazards of environmental contaminants which may include the toxin mercury (Desgranes, et al. 1998). Human encroachment on estuaries and seacoast Habitats as well as shooting are also cited as threats (Terres 1980).
Special Biological Considerations
The species is restricted to fish-bearing waters (Zeiner, et al. 1990). In many areas, up to 80 percent of tree nests occur within 500 meters of open water (Ewins 1997).
The population of ospreys in Finland has been documented to be increasing due to the decrease in persecution pressure during migration (Saurola 1995). Re-introducing ospreys to a metropolitan area is an effective contribution to restoring an ecosystem as well as educating the general public about raptors, wildlife, general ecological principles and the human role in natural resources conservation (Martell 1995).
Certain pesticides were shown to cause reproductive failure (Zeiner, et al. 1990). Since bans on these toxins were passed in the 1970s, there has been a reduction of the DDT-level in osprey eggs and most populations have increased at average rates up to 15 percent per year (Ewins 1997; Saurola 1995).
Ospreys have adapted well to nesting on a wide range of artificial substrates (Ewins 1997). The osprey population has shown an increase resulting from the active construction of artificial nests to compensate for losses of potential nesting trees caused by forestry (Saurola 1995).
The influence of human disturbance of ospreys at their nest seems to vary according to whether the birds are already used to human presence or not, whether the disturbance is regular from the onset of the nesting season or if it commences during a sensitive stage such as the incubation or small chick stage (Ewins 1997). In many areas, ospreys nest very successfully in proximity to humans and it is likely that birds recruiting to such sites have been raised in similar situations. In contrast, reduced breeding success is often experienced by birds disturbed after nesting has begun (Ewins 1997). Management guidelines have been developed to provide buffers for nesting ospreys: absolute buffer zone within a 40 to 200 meter radius of an occupied nest tree where access is restricted year-round and limited activities within the buffer include nest site protection; seasonal buffer zone within a 100-800 meter radius of an occupied nest or up to 600 meter beyond the periphery of the absolute buffer zone and for the duration of the breeding season within which activities such as logging, road or pipeline construction, mining, and some recreation are banned; riparian/lacustrine buffer zone for distances of 70-350 meters back from the water's edge where there may be no cutting and the retention of up to 5 snags and 5 clumps of tall trees (Ewins 1997).
The most important nest site selection criteria currently seems to be a clear aerial access to the nest, at least one strong side branch to support the heavy nest, proximity to water, inaccessibility to mammalian predators, avoidance of bald eagle territories and a nearby elevated perch (Ewins 1997). Ospreys usually build their nests above the surrounding canopy, whether it is 15 meters or 50 meters above ground level. As a result, they tend to select older trees and often dead trees or those with dead, flat or blown-out tops.
It is difficult to know what the population size was historically since more recent forest management often retains trees in shoreline buffer zones primarily for recreational and landscape reasons. Systematic studies of breeding ospreys in relation to different forestry practices and associated activities are needed to provide more consistent, realistic and integrated conservation advice (Ewins 1997).
LITERATURE CITED
Birkhead, T. R. And C. M. Lessells. 1988. Copulation behavior of the osprey Pandion haliaetus. Animal Behaviour 36: 1672-1682.
Call, M. W. 1978. Nesting Habitats and surveying techniques for common western raptors. Technical Note TN-316. U.S. Department of the Interior - Bureau of Land Management, Denver Service Center.
Chubbs, T. E. and P. G. Trimper 1998. The diet of nesting ospreys, Pandion haliaetus, in Labrador. Canadian Field-Naturalist 112: 502-505.
Cleary-Rose, K. 2002. Pers. Comm. U.S. Fish and Wildlife Service.
Desgranges, J. L., J. Rodrigue, B. Tardif, and M. Laperle. 1998. Mercury accumulation and biomagnification in ospreys (Pandion haliaetus) in the James Bay and Hudson Bay Regions of Quebec. Archives of Environmental Contamination and Toxicology 35: 330-341.
Ewins, P. J. 1997. Osprey (Pandion haliaetus) populations in forested areas of North America: changes, their causes and management recommendations. Journal of Raptor Research 31: 138-150.
Flath, D. L. 1972. Canada goose-osprey interactions. Auk 89:446-447.
Garrett, K. and J. Dunn. 1981. Birds of southern California. Los Angeles Audubon Society. 408pp.
Henny, C. J., and R. G. Anthony. 1989. Bald eagle and osprey. Pages 66-82 in B. G. Pendleton (ed.). Proceedings of the Western Raptor Management Symposium and Workshop. National Wildlife Federation, Washington, D.C.
Houston, C. S. and F. Scott. 1992. The effect of man-made platforms on osprey reproduction at Loon Lake, Saskatchewan. J. Raptor Research 26: 152-158.
Houghton, L. M., and L. M. Rymon. 1997. Nesting distribution and population status of U.S. ospreys in 1994. Journal of Raptor Research 31: 44-53.
Kenyon, K. W. 1947. Breeding populations of the osprey in lower California. Condor 49:152-158.
Martell, M. 1995. Osprey Pandion haliaetus reintroduction in Minnesota, USA. Vogelwelt 116: 205-207.
Miller, A. H. and R. C. Stebbins. 1964. The lives of desert animals in Joshua Tree National Monument. University of California Press, Berkeley. 452pp.
Ortega, B. 2001. Pers. Comm. Dudek & Associates.
Poole, A. F., and B. Agler 1987. Recoveries of ospreys banded in the USA. J. Wildlife Management 51: 148-155.
Saurola, P. 1995. Finnish ospreys Pandion haliaetus in 1971-1994. Vogelwelt 116: 199-204.
Seibold, I., A.J. Helbig. 1995. Systematic position of the osprey Pandion haliaetus according to mitochondrial DNA sequences. Vogelwelt 116: 209-217.
Terres, J. K. 1980. The Audubon Society Encyclopedia of North American Birds. Alfred A. Knopf, New York, New York. 1109pp.
Tishechkin, A. K. And V. V. Ivanovsky. 1992. Status and Breeding performance of the osprey Pandion haliaetus in Northern Belarus. Ornis Fennica 69: 14.
Unitt, P. 1984. The birds of San Diego County. San Diego Society of Natural History: Memoir 13, San Diego, California. 276pp.
Witt, J. W. 1996. Long-term population monitoring of osprey along the Umpqua River in western Oregon. Journal of Raptor Research 30: 62-69.
Zeiner, D.C., W. F. Laudenslayer, K. E. Mayer and M. White eds. 1990. California's Wildlife: Volume II - Birds. California Department of Fish and Game. Sacramento, California. 732pp.
peregrine falcon (Falco peregrinus)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
peregrine falcon (Falco peregrinus)
Status:
State: Endangered; Fully-Protected Species; California Department of Forestry and Fire Prevention Sensitive (nesting)
Federal: Delisted from Endangered; Partners in Flight Priority Bird Species. This species was considered endangered throughout its range, Federal Register, June 2, 1970; October 13, 1970; March 20, 1984.
GROUP DESIGNATION AND RATIONALE
Group 1
The peregrine falcon has a wide but sparse distribution throughout the MSHCP Plan Area within its suitable Habitat. Although is nest site is located on the County Building in downtown Riverside, it is predominantly a fall transient with occasional wintering and rare spring transient movements. It occurs or has occurred at almost every open water body within the Plan Area and occurs within the Prado Basin on a regular basis.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 10,340 acres of open water Habitat at the following seven open water bodies and one drainage: Lake Mathews, Diamond Valley Lake, Lake Skinner, Lake Elsinore, Vail Lake, Lake Perris, Mystic Lake/San Jacinto Wildlife Area, and Prado Basin/Santa Ana River and the 5,520 acres of suitable riparian Habitat within the Prado Basin/Santa Ana River.
Objective 2
A 100-meter buffer will be established around open water bodies identified in Objective 1 as they are incorporated into the MSHCP Conservation Area.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
For the purpose of the conservation analysis, potential Habitat for the peregrine falcon includes the foraging Habitat composed of open water and the riparian area within the Prado Basin and Santa Ana River. Based on these Habitats, the Plan Area supports approximately 18,000 acres of potential Habitat for the peregrine falcon. Table 1 shows the conservation and loss of potential Habitat for the peregrine falcon. Overall, approximately 15,860 acres (88 percent) of potential Habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public Lands.
As described below under Data Characterization, 9 of the 17 recent point localities have a high location precision. One nest location is recorded for the County Building in downtown Riverside. Peregrine falcons have been known to nest on buildings within major cities (e.g., Panama; pers. obs. A. Hayworth). Although this nest site is outside of the MSHCP Conservation Area, the provision of suitable Habitat within the MSHCP Conservation Area for foraging will support the nest site. No Take of raptor nest sites, including that of the peregrine falcon, is authorized by the Plan. Of the 9 point localities, 4 (44 percent) will be inside the Criteria Area or Public/Quasi-Public lands. However, of the five points located outside these Habitat areas, all are mapped in existing residential/urban/exotic areas or in existing agriculture. These locations may have been of a bird flying overhead or within Habitat adjacent to one of the reservoirs where they might hunt. Providing suitable foraging Habitat which includes the open water and reservoirs and the riparian area in the Prado Basin and Santa Ana River are important conservation measures.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
PEREGRINE FALCON
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| All Bioregions | |||||||
| Open Water | 12,210 | 1,190 | 9,150 | 10,340 | 40 | 1,830 | 1,870 |
| Riparian Habitat within Prado Basin/Santa Ana River | 5,790 | 510 | 5,010 | 5,520 | 0 | 270 | 270 |
| TOTAL | 18,000 | 1,700 (9%) |
14,160 (79%) |
15,860 (88%) |
40 (<1%) |
2,100 (12%) |
2,140 (12%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
In addition, the Riparian/Riverine Areas and Vernal Pools policy described in Section 6.1.2 provides for conservation of wetlands which provide Habitat for this species through avoidance and minimization. Mitigation for impacts to wetlands shall be incorporated in accordance with the "No Net Loss" policy of federal and state wetland regulations. The proposed mitigation shall be directly related to the functions and values of the wetland as related to this species and result in equivalent replacement.
Conservation of this species will be considered from a landscape perspective because the species is found throughout the Plan Area and predictably uses areas with suitable foraging opportunities and regularly occurs at a number of known locations.
MSHCP Conservation Area Configuration Issues
Several large blocks of Habitat supporting the current known locations and potential foraging locations of the peregrine falcon will be conserved as Criteria Area and Public/Quasi-Public designations, including the Prado Basin, Santa Ana River, Lake Skinner, Diamond Valley Lake, Lake Mathews, Lake Perris, Mystic Lake/ San Jacinto Wildlife Area, Lake Elsinore, and Vail Lake. As identified below, the species occurs within the Plan Area predominantly as a fall transient, occasionally as a winter visitor, and rarely as a spring transient, although one nest site is known for the Plan Area. Additionally, the dispersal distance for the species will allow them to cover the MSHCP Plan Area and they will be capable of dispersing to suitable foraging areas throughout the Plan Area. As such, the MSHCP Conservation Area will provide adequate Habitat for foraging during nomadic visits to the area and migratory stopovers as well as during the breeding season. Foraging areas are provided at Vail Lake, Lake Skinner, Diamond Valley Lake area, Lake Perris, Mystic Lake/San Jacinto Wildlife Area, Lake Elsinore, Lake Mathews, Prado Basin and Santa Ana River. These MSHCP Conservation Area areas are linked as well, however the peregrine falcon, due to its ability to move long distances, may rely less on the linkage than other species.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 10,340 acres of suitable Conserved Habitat including open water at Lake Mathews, Diamond Valley Lake, Lake Skinner, Lake Elsinore, Vail lake, Lake Perris, Mystic Lake/San Jacinto Wildlife Area, and Prado Basin/Santa Ana River and 5,520 acres of suitable Conserved Habitat including riparian Habitat within the Prado Basin/Santa Ana River. The current population size of the peregrine falcon is unknown because it is a casual visitor to the area. There is one nest site currently known for the County Building in downtown Riverside and although this nest site is outside the MSHCP Conservation Area, no Take of raptor nests is authorized. The species appears to respond to elevated waterfowl populations within reservoirs during migration and winter periods. Therefore, local densities will be expected to fluctuate.
INCIDENTAL TAKE
Approximately 2,140 acres (12 percent) of potential Habitat for the peregrine falcon will be outside the Criteria Area and Public/Quasi-Public land designations and individuals within these areas will be subject to Incidental Take consistent with the Plan. Although the one known nest site is located outside of the MSHCP Conservation Area, no Take of raptor nest sites is authorized by the Plan.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The UCR location database includes a total of 22 records of the peregrine falcon dated from 1908 to 1999. The record from 1908 is a museum skin record and the balance of the records are predominantly from local biologists and also from the U.S. Fish and Wildlife Service. A total of 17 of the records are relatively recent (dated within the past 10 years) and of these, 9 are of high precision and could be accurately placed within the Plan Area. These recent and high precision records are all recorded for Habitats within which the species could occur including grassland, riparian, alkali playa, and open water and are all likely to be extant.
The literature available on the peregrine falcon is fairly extensive. It has been studied for many years by ornithologists interested in raptors. Due to its listed status, the pesticide problems to which is attributed its population decline a number of years ago, as well as the interest in captive propagation of the species, a large number of natural history articles as well as summary information is available. The species has always been a high interest species due to its hunting ability and use as a falconry bird. Little information is available that pertains directly to the Plan Area.
Habitat and Habitat Associations
Throughout the species' range, peregrine falcons are found in a large variety of open Habitats, including tundra, marshes, seacoasts, savannahs and high mountains (AOU 1998, Brown 1999). The species breeds mostly in woodland, forest, and coastal Habitats (Brown 1999). Riparian areas and coastal and inland wetlands are important Habitats year-round, especially in non-breeding seasons. During migration, the peregrine falcon may be found near marshes, lakes, and ponds with high concentrations of waterfowl, shorebirds, and other birds. And, like many other migratory birds of prey, during migration, peregrine falcons often travel along mountain ridges on both eastern and western coastlines (Brown 1999).
Within southern California, peregrine falcons are primarily found at coastal estuaries and inland oases where ever a food source is located (Garrett and Dunn 1981).
The Habitat requirements of the American peregrine falcon have been summarized within the Recovery Plan for the species (USFWS 1984). This summary provides a succinct description of the variables and conditions that lead to occupation of an area by the peregrine. Their high mobility, extensive hunting areas, remote, rugged nest sites, and preferences of the individual pairs combine to make it extremely difficult to stereotype and classify the typical peregrine falcon Habitat. The peregrine falcon Habitat requirements are summarized as follows from USFWS (1984):
Nesting Habitat: a cliff, or series of cliffs, generally 200 to 300 feet in height that tends to dominate the surrounding landscape. Mountain valleys and river gorges with precipitous cliffs also are preferred nest sites. Nest sites are usually located below 9,500 feet elevation. An adequate food source is normally found within 10 miles of the nest site.
Hunting Habitat: those areas within 10 miles of the nesting cliff which supply the major portion of the food source (birds) to the peregrine falcon. Other Habitats within 10 to 20 miles of the nesting cliff also may be important hunting areas, but they are often so interspersed or widespread that it is difficult to specifically delineate them. This does not imply that all lands within 10 miles of an eyrie site are to be considered essential Habitat. Examples of important hunting areas are wetlands and riparian Habitats; meadows and parklands; crop lands such as hayfields, grainfields and orchards; and areas such as gorges, mountain valleys and lakes over which prey are vulnerable.
Sites Suitable for Occupancy and/or range Expansion by the Peregrine: Sites (other than those occupied or historical sites) which exhibit the requirements or needs of the peregrine as described above.
Migration and/or Wintering Habitat: wildlife (waterfowl) refuges or other Habitats which concentrate food sources.
Biogeography
The peregrine falcon has a worldwide distribution that is more extensive than any other bird. The species breeds in North America from Alaska east to Labrador southward to southern California and Baja California, central Arizona and Mexico through Alabama. The species winters from southern Alaska to Tierra del Fuego in southernmost South America (AOU 1998). The former breeding range also included Ontario, southern Quebec, the Canadian Maritime Provinces, and the eastern United States, south to northern Georgia. Currently, there may be 500 to 600 peregrine falcon pairs in the western United States but, based on a 1975 survey, the original eastern population has been extirpated and is being re-established through captive propagation (USFWS 1991).
In California, the peregrine falcon breeds and winters throughout the state, with the exception of desert areas (Zeiner, et al., 1990). The peregrine is a very uncommon breeding resident and uncommon as a migrant or as winter resident. Active nesting sites of this species within California are known from along the coast north of Santa Barbara, in the Sierra Nevada, and other mountains of northern California. Three nest sites are known anecdotally for southern Californa: under the Coronado Bridge, at the Salt Works in Chula Vista (Hayworth 1992, pers. obs.), and on the County Building in downtown Riverside (Cleary-Rose 2002, pers. comm.). Some of the individuals that breed farther north migrate into California for the winter months. During this time, peregrines can be seen inland throughout the Central Valley and occasionally on the Channel Islands.
Spring and fall migrants of the peregrine falcon occur along the coast and in the western Sierra Nevada Mountains (Brown 1999). It occurs within the Plan Area primarily as a fall transient, occasionally as a winter visitor and rarely as a spring transient. As a transient species, it may occur almost anywhere within appropriate Habitat (Garrett and Dunn 1981).
Known Population Within Western Riverside County
The peregrine falcon could be expected virtually anywhere within the Plan Area during all seasons. Although peregrines were observed on at least two occasions in the Prado Basin and environs in 1998 (James Pike, USFWS, pers. comm., 1998), the species remains quite scarce elsewhere within the Plan Area (Michael Patten, Riverside County Editor for American Field Notes and Past Secretary, California Bird Records Committee, pers. comm., 1998). There is one known nesting pair located within the Plan Area on the County Building in downtown Riverside (Cleary-Rose 2002, pers. comm).
Other geographic locations recorded for the species within the U.C. Riverside database include: Mystic Lake/San Jacinto Wildlife Area, Lake Perris, Lake Skinner, and Lake Elsinore, all of which may concentrate waterfowl or shorebirds and constitute foraging areas. All of these locations are likely to be visited by the species with some regularity during transient movements through the Plan Area and possibly for wintering.
The peregrine falcon is primarily a rare spring and more common fall transient and a casual visitor during other seasons of the year within the Plan Area. It was formerly much more common in the region and probably concentrated wherever populations of waterfowl occur. Transients through the area have been noted mostly at well-watered areas which concentrate other migrant species. The subspecies that probably occurs within the Plan Area is F. p. anatum, which is the subspecies that would generally be expected to move through the area as a transient species (Garrett and Dunn 1981).
Biology
Genetics: No information is available or was reviewed.
Diet and Foraging: The peregrine falcon typically hunts its prey in the air and prey is either struck to the ground or killed outright by a blow from the talons. They will also pursue prey in a low, fast flight, or attack passing birds from a perch. Some pairs hunt cooperatively with the larger female diving for the prey first and then if successful, eating first from the prey item (Brown 1999). The species may fly 10 to 12 miles from their nest in search of prey which are usually hunted over open Habitat types such as waterways, fields and wetland areas such as swamps and marshes (USFWS 1991). In general, the peregrine falcon frequents bodies of water in open areas with cliffs and canyons nearby for cover and nesting and is located in areas with abundant avian prey (Zeiner, et al. 1990).
The peregrine falcon will primarily eat pigeon-size birds but may feed on large numbers of lemmings and voles when present (Brown 1999). The diet of this species includes jays, flickers, meadowlarks, pigeons, starlings, shorebirds, waterfowl and other readily available species. Due to their larger size, the females may take larger prey items (Zeiner et al. 1990).
Daily Activity: No information is available or was reviewed. The peregrine falcon typically is a diurnally active predator that also migrates during the daytime.
Reproduction: Breeding of the peregrine falcon requires cliffs or suitable surrogates (e.g., buildings) that are close to preferred foraging areas. They have been known to nest in trees and on small outcrops in other portions of their range. Some peregrines have used tall buildings within major cities (e.g., Panama; Hayworth 1988, pers. obs.), bridges or other tall man-made structures for nesting (CDFG 1999). The nest site usually provides a panoramic view of open country, often overlooking water and is always associated with an abundance of columbiform, passerine, waterfowl, or shorebird prey, even in an urban setting. Heller (1992) found a growing population of falcons nesting entirely on power plant towers and quarries. A cliff nest site may be used for many years (Brown 1999). The nest site itself, which is often referred to as an eyrie, usually consists of a rounded depression, or scrape, with accumulated debris that is occasionally lined with grass (Call 1978). Higher quality nest sites tend to confer greater protection from adverse weather and show greater breeding success (Olsen and Olsen 1989).
Breeding of the peregrine falcon occurs from early March to late August. The clutch size varies from three to seven eggs with incubation at 28 to 35 days performed by both parents (Brown 1999). The young typically fledge from the nest between 25 and 42 days (Brown 1999). The young are not independent of the parents for several months. If the first eggs are removed or destroyed early in the season, a second clutch is possible (Brown 1999).
Survival: The hatching success of the peregrine falcon in the wild is about 75 percent. An average of one young reaches fledging per laying pair. The juvenile birds continue to be particularly vulnerable during their first year of life as they learn to hunt and develop flying skills (USFWS 1991). Enderson (1969) estimated annual juvenile mortality at approximately 70 percent and adult mortality at approximately 25 percent. The mean life expectancy for those young that fledge is approximately four years. The maximum life span of the peregrine is in excess of 13 years. It is possible that a few individuals may reach 20 years of age. Due to the long average life expectancy and the population dynamics, a sudden, drastic change in the number of breeding adults should not be expected, even when reproduction is as low as it currently is. Similarly, successful management operations will not likely provide quick population recovery (USFWS 1984).
Dispersal: Little is known of post-breeding movements of peregrine falcon adults or immatures (USFWS 1984). Within the midwest, dispersal from hack or natal sites has a large variation, however the mean dispersal distance of females, at 320 kilometers, is about twice that of males, at 176 kilometers. Fidelity to the territory is strong, but territorial shifts do occur (Tordoff and Redig 1997).
Socio-Spatial Behavior: In the Rocky Mountains, the home range of the peregrine falcon includes the area encompassed by a radius up to 23 kilometers (14 miles) from cliff nests (Zeiner, et al. 1990). Cade (1960) found a minimum territory of about 96 meters (300 feet) radius around peregrine nests in Alaska. White and Cade (1971) reported that the mean spacing between nests was 9.7 kilometers (6 miles) along Alaska rivers. In some parts of California, the home range averages 125 square miles and territories are spaced approximately 3 - 7 miles apart (Zeiner, et al. 1990). The species is most likely to be found where prey (primarily birds) concentrate. In resident birds, pair-bonds remain established year-round (Brown 1999).
Community Relationships: The peregrine falcon competes with ravens and prairie falcons (Falco mexicanus) for nesting sites (Porter and White 1973). Some predation from great horned owls may occur (USFWS 2/91).
Threats to Species
Although formerly critically endangered due to eggshell thinning caused by the organochlorine pesticide DDT, the persecution of the peregrine falcon for falconry and "vermin" control, and Habitat destruction, the North American populations of this species apparently are recovering well.
The principal cause of the peregrine falcon population decline has been due to the presence of chlorinated pesticides, especially DDT and its metabolite DDE. These compounds accumulated in the birds as a result of feeding on contaminated prey. The effect was damage to the reproductive potential through interference with calcium metabolism. The eggs were laid with thin shells, rendering them easily broken and consequently, greatly affecting the species' reproductive success (USFWS 2/91).
Within California, the peregrine falcon population has declined drastically in recent years (Thelander 1975,1976): 39 breeding pairs were known in California in 1981 (Monk 1981). This decline, similar to the decline found in eastern portions of the country, appears to be associated mostly with DDE contamination. The coastal population apparently has been reproducing poorly, perhaps because of heavier DDE load received from the migrant bird prey. A captive rearing program has been established to augment the wild population, and numbers are increasing (Monk 1981).
Special Biological Considerations
A comprehensive recovery plan for the species in the eastern part of the country was completed in 1979, and revised in 1987. The primary objective of the plan is to restore a self-sustaining population of the peregrine falcon in the eastern United States (USFWS 1991). The goal of the recovery plan is to attain a successful, sustained, nesting population in the wild at a level of 50 percent of the numbers estimated to have occurred in the 1940s or to a level that the present environment and Habitat will support. In addition, a minimum of 20 to 25 nesting pairs are to be attained in each of the five regions where this bird is released from a captive breeding program. The recovery plan recommends that these goals for recovery be accomplished by: preserving and providing nesting Habitat; restoring the peregrine population through the introduction of captive-produced birds; preserving migration and wintering Habitat; and providing protection for the birds. In the early 1940s, the eastern United States population was roughly estimated at 350 pairs. As a result of a captive breeding program, a total of 1,178 peregrines have been reintroduced into the northeastern portions of the country. As of 1990, there were a total of 84 territorial pairs, 58 laying pairs, and 45 successful pairs producing a total of 111 young (USFWS 1991). Continuing population increases and the magnitude of continuing recovery efforts by a variety of agencies, organizations, and the interested public prompted the Service to propose the delisting of the species in 1998 (Brown 1999).
In California, from 1977 to 1992, 702 peregrine falcons were released in the wild through the breeding program (CDFG 1999). Wooton and Bell (1992) developed a model for predicting viability of the falcon population given different management strategies. The model fit known yearly data from California between 1980-1989. The model indicated that the California population, given current management techniques, would not be sustainable without further intervention. Furthermore, they predicted that enhancing adult survivorship is more effective than enhancing fledging success and that efforts should be concentrated in northern California where populations are more dense in order to achieve a viable population. Wooton and Bell (1992) predicted that as a viable population, the northern California population would exhibit a source-sink dynamic between subpopulations.
Protective measures have been outlined within the Peregrine Falcon Recovery Plan (USFWS 1984). These include the following measures. Prohibit land-use practices and/or development that will adversely alter or eliminate existing Habitat within one mile of the nesting cliff or site. Prohibit all human activities within one-half mile distance of the nesting cliff between February 1 and September 1 of each year. Retain suitable nesting Habitats in public ownership. Prohibit land-use practices and/or developments which could alter or eliminate the character of the hunting Habitat or food source. Prohibit the use of harmful pesticides and other detrimental environmental pollutants which would accumulate in the peregrine or its food source. Sites suitable for occupancy and/or expansion should be protected and managed accordingly to ensure that the quality of the Habitat is not altered or eliminated. Due to human encroachment and extensive Habitat manipulation, many of the historic peregrine nesting areas have either been eliminated or altered significantly so as to make them unsuitable for nesting. As a result, new sites suitable for occupancy by peregrines must be identified and maintained as early as feasible in order to affect the recovery of the species.
LITERATURE CITED
AOU (American Ornithologists' Union). 1998. Check-List of North American Birds. Seventh Edition. American Ornithologists' Union, Washington, D.C. 829 pp.
Brown, N. L. 1999. World Wide Web-site: http://arnica.csustan.edu/esrpp/pfweb1.htm.
Cade, T. J. 1960. Ecology of the peregrine and gyrfalcon populations in Alaska. Univ. Calif. Publ. Zool. 63:151-290.
California Department of Fish and Game. 1999. World Wide Web-site http://www.dfg.ca.gov/ te_species/index/classification/birdslist/peregrine.html.
Call, M. W. 1978. Nesting Habitats and surveying techniques for common western raptors. Technical Note TN-316. Bureau of Land Management, Denver, Colorado.
Cleary-Rose, K. 2002. Pers. comm. U.S. Fish and Wildlife Service.
Enderson, J. H. 1969. Peregrine and prairie falcon life tables based on band-recovery data. Pages 505-509 In J. J. Hickey, ed. Peregrine falcon populations. Univ. Wisconsin Press, Madison, WI.
Garrett, K. and J. Dunn. 1981. Birds of Southern California: Status and Distribution. Los Angeles Audubon Society. 407 pp.
Grinnell, J. and A.H. Miller. 1944. The Distribution of the Birds of California. Pacific Coast Avifauna Number 27. Cooper Ornithological Club, Berkeley, California. Reprinted by Artemisia Press, Lee Vining, California; April, 1986. 617 pp.
Hamilton, R. and D.R. Willick. 1996. The Birds of Orange County, California: Status and Distribution. Sea and Sage Press, Irvine, California. 150 pp. with appendices.
Hayworth, A. 1988. Pers. obs., University of California, Davis.
Hayworth, A. 1992, Pers. obs. Hayworth Biological Consultants.
Heller, M. 1992. The development of a peregrine falcon populations Falco peregrinus peregrinus breeding on building and quarries in lowlands of Wuerttemberg. Orinthologischer Anzeiger 31: 51-55.
Monk, G. 1981. California peregrine falcon reproductive outcome and management efforts in 1981. U.S. Dep. Inter., Fish and Wildl. Serv., Sacramento. Endang. Spec. Rep. 27pp.
Olsen, P.D. and J. Olsen. 1989. Breeding of the Peregrine falcon (Falco peregrinus): III. Weather, nest quality and breeding success. EMU 89:6-14.
Patten, M. 1998. Pers. comm. Riverside County Editor for American Field Notes and Past Secretary, California Bird Records Committee
Pike, J. 1998. Pers. comm., U.S. Fish and Wildlife Service.
Porter, R. D., and C. M. White. 1973. The peregrine falcon in Utah, emphasizing ecology and competition with the prairie falcon. Brigham Young Univ., Provo. Sci. Bull. Biol. Ser. 18. 74pp.
Sexton, C.W. and G.L. Hunt. 1979. An annotated checklist of the birds of Orange County, California. University of California Irvine Museum of Systematic Biology Research Series No. 5.
Thelander, C. G. 1975. Distribution and reproductive success of peregrine falcons (Falco peregrinus anatum) in California, 1975. Calif. Dept. Fish and Game, Sacramento. Wildl. Manage. Branch Admin. Rep. 75-6. 12pp.
Thelander, C. G. 1976. Distribution and reproductive success of peregrine falcons (Falco peregrinus anatum) in California during 1975-1976. Calif. Dept. Fish and Game, Sacramento. Wildl. Manage. Branch Admin. Rep. 76-3. 13pp.
Tordoff, H. B., and P. T. Redig. 1997. Midwest peregrine falcon demography, 1982-1995. J. Raptor Research 31: 339-346.
USFWS. 1984. American Peregrine Falcon Recovery Plan (Rocky Mountain/southwest Population). Prepared in cooperation with the American peregrine falcon recovery team. USFWS, Denver, Colorado.
USFWS. February 1991. Endangered and threatened Species of the Southeastern United States (The Red Book) FWS Region 4.
White, C. M., and T. J. Cade. 1971. Cliff-nesting raptors and ravens along the Colville River in arctic Alaska. Living Bird 10:107-150.
Willett, G. 1933. Revised list of the birds of southwestern California. Pacific Coast Avifauna No. 21.
Wooton, J.T. and D.A. Bell. 1992. A metapopulation model of the peregrine falcon in California: Viability and management strategies. Ecological Applications 2: 307-321.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
prairie falcon (Falco mexicanus) - breeding
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
prairie falcon (Falco mexicanus) - breeding
Status:
State: Species of Special Concern
Federal: Partners in Flight Priority Bird Species; San Bernardino National Forest Sensitive
Other: Audubon Society California Watch List
GROUP DESIGNATION AND RATIONALE
Group 1
The prairie falcon has a wide but sparse distribution over many Habitat types within the Plan Area. There is one clumped distribution within the Mystic Lake/San Jacinto Wildlife area. No nest sites are known for the area although one could be present within the Vail Lake area and one may have been historically present possibly within the Lakeview Mountains area.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 141,510 acres of suitable open and scrub Habitats including grassland, playa and vernal pool, Riversidean alluvial fan sage scrub, coastal sage scrub, and desert scrubs. Conservation will occur in large blocks throughout the Plan Area, including at a minimum: Mystic Lake/San Jacinto Wildlife Area (2,690 acres), Lakeview Mountains (7,150 acres), and Vail Lake (12,320 acres).
SPECIES CONSERVATION ANALYSIS
Conservation Levels
The prairie falcon uses predominantly open land including grassland with use of some other Habitats including alluvial, playa, and sparse coastal sage scrub and chaparral, and desert scrub (Garrett and Dunn 1981). The prairie falcon potentially breeds in very few locations, has not been recently documented to breed within the Plan Area, and may winter sporadically in the Plan Area. For the purpose of the conservation analysis, potential Habitat for the prairie falcon includes foraging Habitats including grassland, playa and vernal pool, Riversidean alluvial fan sage scrub, coastal sage scrub, and desert scrubs and cliff conditions for nesting. Based on these Habitats, the Plan Area supports approximately 324,000 acres of potential Habitat for the prairie falcon. Table 1 shows the conservation and loss of potential Habitat for the prairie falcon. Overall, approximately 141,510 acres (44 percent) of potential Habitat in the planning area will be conserved in Criteria Area or existing Public/Quasi-Public Lands. Management actions will be incorporated into the conservation strategy so that suitable Habitat conditions will be maintained.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
PRAIRIE FALCON
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| Grassland | 146,870 | 20,010 | 22,810 | 42,820 | 12,220 | 91,830 | 104,050 |
| Playas and Vernal Pools | 7,910 | 3,830 | 2,920 | 6,750 | 0 | 1,160 | 1,160 |
| Desert Scrubs | 9,380 | 3,680 | 1,310 | 4,990 | 40 | 4,350 | 4,390 |
| Riversidean Alluvial Fan Sage Scrub | 7,150 | 3,170 | 2,060 | 5,230 | 220 | 1,700 | 1,920 |
| Coastal Sage Scrub | 152,690 | 47,160 | 34,560 | 81,720 | 26,240 | 44,730 | 70,970 |
| TOTAL | 324,000 | 77,850 (24%) |
63,660 (20%) |
141,510 (44%) |
38,720 (12%) |
143,770 (44%) |
182,490 (56%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
As described below under Data Characterization, 13 of the 35 recent point localities have a high location precision of "1." Of these 13 point localities, 5 will be inside the Criteria Area or Public/Quasi-Public lands. A total of 8 point localities will be outside of the MSHCP Conservation Area. The two potential or historic nest locations, Vail Lake and Lakeview Mountains, will be conserved. The population concentration at Mystic Lake/San Jacinto Wildlife Area will be conserved. Some of the scattered and infrequent records present in the Badlands area, Lake Perris, Lake Skinner, French Valley, and Alberhill areas, and along the northwestern portion are likely wintering records and will be conserved. There are definable locations for focusing conservation efforts where the species has potential or historic nest locations within the Lakeview Mountains and Vail Lake areas.
MSHCP Conservation Area Configuration Issues
Several large blocks of Habitat supporting the current known and potential foraging and potential or historic nesting locations of the prairie falcon will be conserved as Criteria Area and Public/Quasi-Public, including the Vail Lake, Lakeview Mountains, and Mystic Lake/San Jacinto Wildlife Area. As identified above, the species occurs within the MSHCP Plan Area as a year round resident, with opportunities for breeding. As such, the MSHCP Conservation Area will provide adequate Habitat for nesting and foraging.
Conservation Summary
In summary, conservation of this species will be achieved by inclusion of at least 141,510 acres of suitable Conserved Habitat including grassland, playa and vernal pool, Riversidean alluvial fan sage scrub, coastal sage scrub, and desert scrubs. In addition, several large blocks of Habitat supporting the current known and potential foraging and potential or historic nesting locations of the prairie falcon will be conserved in the MSHCP Conservation Area, including the Vail Lake, Lakeview Mountains, and Mystic Lake/San Jacinto Wildlife Area. Although it occurs repeatedly in a number of conserved locations, the current population size of the prairie falcon in the Plan Area is unknown.
INCIDENTAL TAKE
Approximately 182,490 acres (56 percent) of potential Habitat for the prairie falcon will be outside the MSHCP Conservation Area and individuals within these areas will be subject to Incidental Take consistent with the Plan.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The location database for the prairie falcon includes approximately 65 data records ranging in date from 1900 through 1999. Thirty-five of these are dated recently, since 1990, and a total of 13 of these are high precision to specify the location with accuracy. These data points show a correlation with chaparral, sage scrub, open water, alkali playa, and non-native grassland. Two of the high precision and recent data points are associated with residential land use and may no longer be suitable Habitat.
A moderate amount of literature is available for the prairie falcon because it is a bird of prey and due to its use as a falconry bird. Most of the literature pertains to general natural history and the falcons in general. Few controlled scientific studies have been conducted, however some management studies are available. Very little information is available for the Plan Area other than what is available regarding basic distribution information.
Habitat and Habitat Associations
Habitat use of the prairie falcon includes annual grasslands to alpine meadows. The prairie falcon is associated primarily with perennial grasslands, savannahs, rangeland, some agricultural fields during the winter season, and desert scrub areas, all typically dry environments of western North American where there are cliffs or bluffs for nest sites (Brown and Amadon 1968). Steenhof (1998) summarized the Habitat use as shrub-steppe desert, grasslands, mixed shrub and grasslands, alpine tundra, desert grassland, chaparral, creosote bush, and bursage Habitat. The species requires sheltered cliff ledges for cover and nesting which may range in height from low rock outcrops of thirty feet to vertical, 400 feet high (or more) cliffs and typically overlook some treeless country for hunting (Call 1978). Denton (1975) reported 76 percent of eyries had water within 0.4 km (0.25 mi). It uses open terrain for foraging; it nests in open terrain with canyons, cliffs, escarpments, and rock outcrops. They capture prey most often in areas of low (less than 30 centimeters), sparse vegetation (Steenhof 1998). The elevation of their Habitat use includes open Habitat up to 3,350 meters (Steenhof 1998). They winter mostly in the great plains and great basin and most winter recovery locations of individuals banded in Canada were in grassland Habitats, mainly in the Great Plains, but also in areas west of the Rockies; only 2 of 48 recoveries were in forested Habitat (Schmutz et al. 1991).
Biogeography
The breeding range of the prairie falcon includes southern central British Columbia, southern Alberta, and southernmost Saskatchewan, east to the badlands and plains of western North Dakota and extreme western Nebraska south to Chihuahua, Coahuila, central Durango, and San Luis Potosi, Mexico (Steenhof 1998). The species winters east to Minnesota, northwestern Iowa, east-central Missouri, central Oklahoma, and most of Texas, to Vancouver, British Columbia, the coasts of Washington, Oregon, and California, all of Baja California and as far south as central Mexico (Steenhof 1998).
Data on population sizes are not available before 1950, however, the current data show significant increasing trends for the species continent wide. Representatives from wildlife agencies in six western states characterized populations of the prairie falcon as "stable" in 1987 and the species is classified as "not at risk" in Canada because of stable or increasing numbers. Early reports of declines in California have been countered by more recent assessments of population stability (Steenhof 1998).
In California, the prairie falcon is an uncommon permanent resident and migrant that ranges from southeastern deserts northwest along the inner Coast Ranges and Sierra Nevada (Garrett and Dunn 1981). It is distributed from annual grasslands to alpine meadows within this region. It is not found in the northern coastal fog belt, or along the coastline. Migrants from northern areas winter in California. Some residents wander up slope in summer and down slope for winter (Zeiner et al. 1990).
Known Populations Within Western Riverside County
The prairie falcon has been documented as occurring within the Santa Ana Mountains during the wintering season and as a year-round resident throughout the rest of the western Riverside County area from the central portion to the eastern boundary (Zeiner, et al. 1990). Location records from UCR show the general distribution as dominating the central part of the Plan Area with few records in the western or eastern mountainous areas and no records in the southeastern portion. The lack of record locations in the southeastern area may reflect low survey effort rather than lack of use of the area. There is a predominance of location records in the Mystic Lake/ San Jacinto Wildlife Area. Scattered and infrequent records are present in the Moreno Valley, Badlands, Beaumont/Banning area, Lake Perris, Lake Skinner, French Valley, Vail Lake, and Alberhill areas. Other location records are scattered along the northwestern portion. All of these locations are likely wintering observations although this has not been confirmed. A breeding record is documented historically for the Hemet area (possibly Lakeview Mountains) and potentially in the Vail Lake area. No other breeding activity is known within the Plan Area (P. Bloom, pers.com.).
Biology
Genetics: Chromosomal studies suggest that the prairie falcon has a closer relationship to the peregrine falcon than to the gyrfalcon. Prairie falcons have been hybridized in captivity with both peregrine falcons and gyrfalcons using artificial insemination and they hybridize naturally in the wild with the peregrine falcon (Schmutz and Oliphant 1987).
Diet and Foraging: The prairie falcon eats mostly small mammals, some small birds, and reptiles (Zeiner, et al. 1990). Ground squirrels are a key prey item during the breeding season in most areas and horned larks and western meadow larks are secondary prey species in most breeding areas (Steenhof 1998). Birds, however, are a principal prey of nesting prairie falcons in California (Fowler 1931). It catches prey in the air and on the ground in open areas. It dives from a perch with rapid pursuit, or dives from a searching flight 15-90 m (50-300 ft) above ground. During pre-incubation, incubation, and brood-rearing, the male delivers 97.5, 95.3, and 70.2 percent respectively of the prey with the dominant prey item being ground squirrels (Holthuijzen 1990). The prey is frequently cached and then retrieved at a later time which presumably maximizes food intake and dampens fluctuations in prey availability (Holthuijzen 1990). Prairie falcons have been found to be the most specialized in their diet when compared to other Wyoming raptors (Maclaren, et al. 1988).
Daily Activity: The prairie falcon forages mostly in the early morning and late afternoon except when feeding nestlings or prey is scarce (Zeiner et al. 1990). Much of its time is spent perching near the eyrie (Zeiner et al. 1990).
Reproduction: The prairie falcon usually nests in a scrape on a sheltered ledge of a cliff overlooking a large, open area, and may nest in a crevice or hole in a cliff, a pothole or larger cave (Call 1978). It sometimes nests on an old raven or eagle stick nest on a cliff, bluff, or rock outcrop but never builds a stick nest themselves (Craighead and Craighead 1956). Although, usually the nest is located in the scrape and abandoned stick nests as described, they have been documented to nest in stick nests on electrical power transmission towers (Bunnell et al. 1997). Usually the nests are on south-facing cliffs which may be advantageous when temperatures are low during incubation and brood-rearing in the northern parts of the breeding range (Enderson 1964). In the lower deserts, at the southern end of the range, the falcons may select nest sites to avoid high temperature, thus most nest sites have a microclimate that buffers the nestlings from temperature extremes. The cliff walls act as a heat sink during the day and a heat source at night and overhangs probably offer protection from storms and from hot sun in later parts of the season (Steenhof 1998). Prairie falcons usually have alternate nesting sites located on the same cliff or adjacent cliffs and they exhibit a tendency to use alternate ledges in succeeding years (Call 1978). Aerial courtship display occurs near the nest site. A southeast-facing nest site apparently is preferred, but the height and orientation are secondary to the nature and character of the ledge.
The prairie falcon breeds from mid-February through mid-September, with a peak in April to early August. It establishes the nesting territory in late February through March in most of the breeding range and egg laying begins as early as March in some areas (Steenhof 1998). The clutch size is 3-6 eggs, with an average of 5. The mean laying date for 280 records from 1900-1977 was April 4-11 (Walton 1977). Fledging success over 5 years for 135 nests averaged 3.2 young, ranging from 0-5; 19 percent of the nests had 5 young (Walton 1977). The young begin to disperse in June and July. Successful pairs range over smaller areas than non-nesters and unsuccessful pairs (Marzluff, et al. 1997).
Survival: The survival of prairie falcon nestlings has been observed to be relatively consistent even when the prey abundance varies: mortality in two different years was determined to be 28 and 34 percent (McFadzen and Marzluff 1996a). They may live as long as 13-20 years (Enderson 1969, Denton 1975). The lifetime reproductive output was estimated as 12.3 young for males and 9.8 young for females (Steenhof 1998). Estimates of adult survival rates range from 65 to 81 percent (Denton 1975).
Dispersal: The dispersal period of the prairie falcon from the natal territory and emigration from the breeding area may be significantly lengthened if there is low ground squirrel abundance and the prairie falcon adults are forced to switch to alternate prey sources to feed the young (McFadzen and Marzluff 1996b). Prairie falcons appear to leave their natal territories immediately after the nesting season and apparently use widely separated nesting, post-nesting and wintering areas and then show a tendency to return to breed in the general area where they were hatched (Steenhof et al. 1984).
The prairie falcon has a widely separated nesting, post-nesting and wintering area. It is more a wanderer than a true migrant. Seasonal movements reflect responses to changing food availability throughout the year and band recoveries suggest eastward as well as southward movements (Steenhof et al. 1984; Schmutz et al. 1991).
Socio-Spatial Behavior: The territory and home range of the prairie falcon are probably the same, and males and females differ little in their use of space (Marzluff et al. 1997). The prairie falcon intensively defends its territory. The breeding territory was 5.7 to 6.5 square kilometers (2.2 to 2.5 square miles) in Utah (Smith and Murphy 1973). Active nests have been recorded within 200 meters (636 feet) of one another in sites where individuals did not confront or see each other regularly (Enderson 1964, Garrett and Mitchell 1973). Thus, relative orientation of potential nest site is probably more important than the actual distance from another potential site.
Community Relationships: Egg and nestling predation of the prairie falcon occurs at sites accessible to mammalian predators, great horned owls, and golden eagles (McFadzen and Marzluff 1996a). They may compete with red-tailed hawks for food and nest sites, and with great horned owls and ravens for nest sites. Although competition with other species for nest sites may occur, they are frequently found in close proximity to other raptor species and may actually benefit from nesting near ravens. They may benefit by being able to use abandoned raven stick nests and the ravens may benefit from use of food cached by the prairie falcon, thus the relationship may be considered to be mutually beneficial (Steenhof 1998). Diet overlap ranges from 59 to 99 percent between the other species occurring within a Plan Area in Wyoming including red-tailed hawks, golden eagles, and ferruginous hawks (Maclaren et al. 1988). Those pairs nesting near Habitat most suitable for ground squirrels range over smaller areas than those nesting farther from such Habitat (Marzluff et al. 1997).
Threats to Species
The prairie falcon is harvested legally in 19 states for falconry and although the harvests probably do not affect the population size, it may affect some local population parameters adversely such as territory fidelity (Steenhof 1998). They are vulnerable to DDE poisoning and are more sensitive to DDE than the peregrine falcon and merlin (Remsen 1978). Because the prairie falcon eats more mammals and fewer birds than the peregrine falcon and merlin, it is less exposed or organochlorine pesticides and did not experience severe population declines as did the other two species (Steenhof 1998).
Populations levels of the prairie falcon, especially because the numbers are relatively small, are vulnerable to Habitat change that could reduce their prey populations (Kirk and Hyslop 1998). They are susceptible to Habitat loss on breeding areas because the nesting distribution is closely tied to cliffs. Because the number of nest sites is finite and nonrenewable, pairs cannot move to other undisturbed areas when nest sites or foraging Habitats adjacent to cliffs are destroyed (Steenhof 1998).
Special Biological Considerations
Overall prairie falcon reproductive rates are tied closely to annual indices of ground squirrel abundance but precipitation before and during the breeding season was related inversely to some measures of reproduction (Steenhof, et al. 1999). Military training activities in the Plan Areas appear to have likely interacted with fire and livestock grazing to create less than favorable foraging opportunities for prairie falcons in a large part of the area. Based on this study, to maintain prairie falcon populations, managers should suppress wildfires, restore native plant communities and regulate potentially incompatible land uses (Steenhof, et al. 1999).
The prairie falcon was observed to range over a large area (approximately 300 square kilometers) and increased their foraging ranges in response to declining ground squirrels. They were observed to switch their prey to reptiles and birds when squirrels were rare (Marzluff, et al. 1997).
The prairie falcon was determined to be scarce on plots within Colorado that included significant amounts of urban Habitat with a critical landscape threshold at about 5 to 7 percent urbanization (Berry, et al. 1998).
Overall, the salient features of prairie falcon home ranges result largely from the patchy distribution of landscape features associated with different densities and availabilities of their ground squirrel prey (Marzluff, et al. 1997).
Human disturbance activities may elicit various responses from wildlife and differences in persecution histories result in diverse wildlife responses to different activity types. The prairie falcon is more likely to flush when approached by a human on foot than when approached by an automobile (Holmes et al. 1993). For prairie falcons, walking disturbances on paved roads resulted in shorter flight distances than a similar disturbance on gravel roads. Presumably, raptors perched along paved roads have habituated to the greater traffic volume associated with paved roads. Alternatively, individuals with greater tolerance limits to disturbance may be using areas with greater disturbance levels. Spatial buffer zones are commonly used to protect nesting sites from disturbance, however, buffer zones for wintering raptors also could be effective if placed around sensitive foraging areas. From this study, a buffer zone that would prevent flushing by approximately 90 percent of the wintering individuals of prairie falcons would be set at 160 meters (Holmes et al. 1993). This information may have important implications when addressing the potential impacts from hiking trails within breeding territories of the prairie falcon. Prairie falcons have also been documented as using similar sized foraging territories near oil wells compared to more pristine locations and also included oil well activity areas within their foraging range (Squires, et al. 1993). Other potential human intrusion impacts, including low level aircraft flights and sonic booms also showed no changes or reduction in reproductive success for prairie falcons (Ellis, et al. 1991). However, Call (1978) indicated that they generally tolerate very little human disturbance at the nest site and abandon eyries where excessive human disturbance occurs.
Management of the species has involved four general strategies including maintaining and enhancing availability of nest sites; managing foraging areas to provide Habitat for prey; providing protection from human disturbance; and restoring populations in areas where the species has been reduced or extirpated. Construction of artificial nest sites has been effective in cliff areas where nest sites are limited. Limiting the types and levels of human activity near nests has been a common management strategy throughout the prairie falcon's range, including restricting activities within one kilometer of the nest site although some activities, such as blasting are apparently acceptable within 125 meters of a nest (Steenhof 1998).
In California, captive-bred prairie falcon nestlings were fostered into an occupied nest site in an area where nesting populations had declined (Granger 1977).
LITERATURE CITED
Berry, M. E., C. E. Bock, and S. L. Haire. 1998. Abundance of diurnal raptors on open space grasslands in an urbanized landscape. Condor 100: 601-608.
Bloom, P. 2001. Pers. Comm.
Brown, L., and D. Amadon. 1968. Eagles, hawks and falcons of the world. 2 Vols. Country Life Books, London. 945pp.
Bunnell, S. T., C. M. White, D. Paul, S. D. Bunnell. 1997. Stick nests on a building and transmission towers used for nesting by large falcons in Utah. Great Basin Naturalist 57: 263-267.
Call, M. W. 1978. Nesting Habitats and surveying techniques for common western raptors. Technical Note TN-316. Bureau of Land Management, Denver, Colorado.
Craighead, J. J., and F. C. Craighead, Jr. 1956. Hawks, owls and wildlife. Stackpole Books, Harrisburg, PA. 443pp.
Denton, S. J. 1975. Status of prairie falcons breeding in Oregon. M.S. Thesis, Oregon State Univ., Corvallis. 58pp.
Ellis, D. H, C. H. Ellis, and D. P. Mindell. 1991. Raptor responses to low-level jet aircraft and sonic boom. Environmental pollution 74: 53-84.
Enderson, J. H. 1964. A study of the prairie falcon in the central Rocky Mountain region. Auk 81:332-352.
Enderson, J. H. 1969. Peregrine and prairie falcon life tables based on band recovery data. Pages 505-509 in J. J. Hickey, ed. Peregrine falcon populations. Univ. Wisconsin Press. Madison. 596pp.
Fowler, F. H. 1931. Studies of food and growth of the prairie falcon. Condor 33: 193-201.
Garrett, R. L., and D. J. Mitchell. 1973. A study of prairie falcon populations in California. Calif. Dep. Fish and Game, Sacramento. Admin. Rep. 73-2. 15pp.
Granger, S. E. 1977. Re-introduction of captive-bred prairie falcons in California - 1976. Raptor Research 11: 73.
Holmes, T. L., R. L. Knight, L. Stegall, and G. R. Craig. 1993. Responses of wintering grassland raptors to human disturbance. Wildlife Society Bulletin 21: 461-468.
Holthuijzen, A. M. A. 1990. Prey delivery, caching, and retrieval rates in nesting prairie falcons. Condor 92: 475-484.
Kirk, D. A., and C. Hyslop. 1998. Population status and recent trends in Canadian raptors: A review. Biological Conservation 83: 91-118.
Maclaren, P. A., S. H. Anderson, and D. E. Runde. 1988. Food habits and nest characteristics of breeding raptors in southwestern Wyoming (USA). Great Basin Naturalist 48: 548-553.
Marzluff, J. M., B. A. Kimsey, L. S. Schueck, M. E. McFadzen, M. S. Vekasy, and J. C. Bednarz. 1997. The influence of Habitat, prey abundance, sex, and breeding success on the ranging behavior of prairie falcons. Condor 99: 567-584.
McFadzen, M. E. And J. M. Marzluff. 1996a. Mortality of prairie falcons during the fledgling-dependence period. Condor 98: 791-800.
McFadzen, M. E. And J. M. Marzluff. 1996b. Behavior of prairie falcons (Falco mexicanus) during the nesting and fledging-dependence periods under fluctuating prey conditions. Bird Behavior 11: 81-89.
Remsen, J. V., Jr. 1978. Bird species of special concern in California. Calif. Dep. Fish and Game, Sacramento. Wildl. Manage. Admin. Rep. No. 78-1. 54pp.
Schmutz, S. M., and L. W. Oliphant. 1987. Chromosome study of peregrine, prairie, and gyrfalcons with implications for hybrids. J. Hered. 78: 388-390.
Schmutz, S. M., R. W. Fyfe, U. Banasch, and H. Armbruster. 1991. Routes and timing of migration of falcons banded in Canada. Wilson Bulletin 103: 44-58.
Smith, D. G., and J. R. Murphy. 1973. Breeding ecology of raptors in the eastern Great Basin of Utah. Brigham Young Univ., Provo. Sci. Bull. Biol. Ser. 18, No. 3. 76pp.
Steenhof, K. 1998. Prairie Falcon (Falco mexicanus). In The Birds of North America, No. 205 (A. Poole and F. Gill, eds.). The Academy of Natural Sciences, Philadelphia, and The American Ornithologists' Union, Washington, D.C.
Steenhof, K., M. N. Kochert, M. Q. Moritsch. 1984. Dispersal and migration of southwestern Idaho (USA) raptors. Journal of Field Ornithology 55: 357-368.
Steenhof, K., M. N. Kochert, L. B. Carpenter, R. N. Lehman. 1999. Long-term prairie falcon population changes in relation to prey abundance, weather, land uses and Habitat conditions. Condor 101: 28-41.
Squires, J. R., S. H. Anderson, and R. Oakleaf. 1993. Home range size and Habitat-use patterns of nesting prairie falcons near oil developments in northeastern Wyoming. Journal of Field Ornithology 64: 1-10.
Walton, B. J. 1977. Development of techniques for raptor management with emphasis on the peregrine falcon. Calif. Dep. Fish and Game, Sacramento. Admin. Rep. 77-4. 26pp.
Zeiner, D.C., W. F. Laudenslayer, K. E. Mayer and M. White eds. 1990. California's Wildlife: Volume II - Birds. California Department of Fish and Game. Sacramento, California. 732pp.
purple martin (Progne subis)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
purple martin (Progne subis)
Status:
State: Species of Special Concern
Federal: Partners in Flight Priority Bird Species; San Bernardino National Forest Sensitive
Other: Audubon Society Special Concern
GROUP DESIGNATION AND RATIONALE
Group 3
The purple martin has been recorded in very low numbers spread widely over the Plan Area. Almost all of the observations are of migrating individuals except for the vicinity of the known nesting locations and potential nesting locations. It will forage on the wing in a variety of Habitats during migration, however, it has very specialized nest site requirements that are not clearly defined. It is typically found in association with water, either within a drainage or open water body. Potential nesting areas occur in riparian, oak woodland, and montane coniferous Habitats, however, only two nest sites are documented within Habitats that are widespread within the Plan Area. The two recorded nest sites within the Plan Area including Dripping Springs (near Vail Lake) and Thomas Mountain (south of Hemet Lake). There is one historic nest site at Hemet Lake for which the current status is unknown. A possible nest site may be present within the Cleveland National Forest near the western boundary of the Plan Area. Because the purple martin requires specific and undefined conditions for its nesting location which apparently occur rarely within a broadly distributed variety of Habitats, the purple martin will require conservation on a landscape level to provide general foraging and nesting Habitat, site specific considerations to conserve nest site locations, and species specific management conditions.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area 45,020 acres of suitable nesting and foraging Habitat for the purple martin including riparian scrub, forest, and woodland, deciduous woodland and forest, and montane coniferous forest.
Objective 2
Include within the MSHCP Conservation Area the 2 Core Areas including Dripping Springs (represented by Vail Lake Subunit 3 of Southwest Area Plan; 12,320 acres) and Thomas Mountain (represented by the San Bernardino National Forest; 149,750 acres).
Objective 3
Include within the MSHCP Conservation Area micro-Habitat (i.e., groups of large snags) in potential nesting Habitat.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
For the purpose of the conservation analysis, potential Habitat for the purple martin includes riparian scrub, woodland, and forest Habitat, oak woodland and forest, and montane coniferous forest. These Habitat types provide foraging Habitat during winter migratory movements as well as potential and known breeding location Habitat. Based on these Habitats, the Plan Area supports approximately 62,830 acres of potential Habitat for the purple. Table 1 shows the conservation and loss of potential Habitat for the purple martin. Overall, approximately 45,020 acres (72 percent) of potential Habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public Lands.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
PURPLE MARTIN
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| San Jacinto Foothills, Santa Ana Mountains, San Bernardino Mountains, and San Jacinto Mountains | |||||||
| Riparian Scrub, Woodland, Forest | 3,520 | 1,340 | 1,600 | 2,940 | 210 | 370 | 580 |
| Oak Woodlands and Forests | 29,520 | 1,720 | 19,960 | 21,680 | 4,590 | 3,250 | 7,840 |
| Montane Coniferous Forest | 29,790 | 20 | 20,380 | 20,400 | 40 | 9,350 | 9,390 |
| TOTAL | 62,830 | 3,080 (5%) |
41,940 (67%) |
45,020 (72%) |
4,840 (8%) |
12,970 (21%) |
17,810 (28%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
The two known locations that are currently used for breeding are within the Public/Quasi-Public Lands and will be conserved. One location is at Dripping Springs and one is at Thomas Mountain within the San Bernardino National Forest. Additionally, the potential nest site in the Cleveland National Forest near the western boundary of the Plan Area will be conserved as described below. The purple martin uses cavity nest sites that have been constructed by some other species and as such the nest sites are in limited supply. Species specific conservation measures for the purple martin include conservation of areas within this potential Habitat that contain groups of snags which provide the micro-Habitat that is preferred by this species. Two non-native species, the house sparrow (Passer domesticus) and European Starling (Sturnus vulgaris), are known as aggressive competitors with the purple martin for nest sites. The species specific conservation measures for the purple martin also include monitoring the two known nest sites to determine if house sparrows or European starlings are competing for the nest cavities. If competition is occurring, removal of house sparrows or European starlings may be required in order to allow breeding of the purple martin to proceed.
This species may occur within Forest Service lands for nesting within riparian scrub, woodland, and forest, oak woodland and forest, or montane coniferous forest. Currently, the location within the Cleveland National Forest Service is unknown, however, it may be located near the western boundary of the Plan Area within the Cleveland National Forest. The nesting location within the San Bernardino National Forest has been documented to be at Thomas Mountain. Suitable Habitat areas will be surveyed to determine the status and location of purple martin nest site(s). Protection of the site may be required to avoid human intervention with nesting of the species. Locations of timber harvest may need to be revised and eliminated near nesting sites in order to protect the nest sites within Forest Service lands. Additionally the Forest Service may need to provide control of house sparrows or European starlings if these species are competing with the purple martin for nesting cavities.
In addition, the Riparian/Riverine Areas and Vernal Pools policy described in Section 6.1.2 (MSHCP Volume 1) provides for conservation of wetlands, including riparian Habitat and trees which may be potential nesting trees and which provide Habitat for this species. This conservation of wetlands is through avoidance and minimization. Mitigation for impacts to wetlands shall be incorporated in accordance with the "No Net Loss" policy of federal and state wetland regulations. The proposed mitigation shall be directly related to the functions and values of the wetland as related to this species and result in equivalent replacement.
As described below under Data Characterization, 4 of the 8 relatively recent point localities have a high location precision. Of these 4 point localities, 1 will be inside the Criteria Area, 1 is located within Public/Quasi-Public Lands and 2 will be outside the MSHCP Conservation Area. The number of locations documented within the UCR database is not sufficient to analyze and it is possible that all locations are of migrating birds or of birds in flight. Of greater importance for analysis of specific locations of the purple martin is the location of nesting sites. All of the known breeding locations and the potential breeding site are located within Criteria Area and Public/Quasi-Public areas. The historic location near Hemet Lake may be outside the MSHCP Conservation Area, however, the status of this location is unknown (Garrett and Dunn 1981). Conservation of this species will be considered from a landscape perspective for conserving potential Habitat for foraging and nesting due to the fact that the suitable Habitat has been defined. Additionally, the specific nest site locations will also be addressed and conserved because they are uncommon. In addition, there are definable areas for focusing conservation efforts including open water areas for foraging (Vail Lake, Lake Elsinore, Lake Mathews/Estelle Mountain, Lake Perris/San Jacinto Wildlife Area, and Lake Skinner) and the known Core Areas composed of the nest sites at Dripping Springs (represented by Vail Lake Subunit 3 of Southwest Area Plan; 12,320 acres) and Thomas Mountain (represented by the San Bernardino National Forest; 149,750 acres) and a potential nesting location in Cleveland National Forest. The total acreage within the Core Areas is 162,070 acres.
MSHCP Conservation Area Configuration Issues
Several large blocks of Habitat supporting or potentially supporting the purple martin for breeding, foraging, or migratory movement will be conserved as Criteria Area and Public/Quasi-Public designations, including the Prado Basin, Santa Ana River, Lake Mathews-Estelle Mountain, Cleveland National Forest, Lake Skinner-Diamond Valley Lake, San Jacinto Wildlife Area/Lake Perris, Vail Lake/Wilson Valley, Lake Elsinore, and the San Bernardino National Forest. Protection is also provided within Cleveland National Forest and San Bernardino National Forest roadless areas and wilderness areas. Some of the large blocks of Habitat have not been mapped as containing purple martins either due to lack of surveys, lack of documentation of observations, or lack of use of the area. However, these Habitat blocks may have suitable breeding and foraging Habitat and could be occupied by purple martins in the future. As a long-distance migrant and a species with a large foraging area and great abilities of flight, purple martins are likely able to discover and use patches of riparian or woodland Habitat that have not been documented to be used in the past. As such, the MSHCP Conservation Area will provide adequate foraging and migratory stopover Habitat as well as snags within potential forested nesting Habitat.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 45,020 acres of suitable Conserved Habitat in the MSHCP Conservation Area. Additionally 162,070 acres of Core Areas including the two documented nest sites and the one potential nest site within large blocks of Habitat will be included in the MSCHP Conservation Area. Implementation of Objective 3 for this species will conserve the micro-Habitat (i.e., groups of large snags) in potential nesting Habitat of the purple martin.
INCIDENTAL TAKE
About 17,810 acres (about 28 percent)of potential Habitat for the purple martin will be outside the Criteria Area and Public/Quasi-Public designations, and individuals within these areas will be subject to Incidental Take consistent with the Plan. Of this, approximately 4,840 acres (8 percent) will be within Rural/Mountainous designation areas. Although these areas will not be part of the managed MSHCP Conservation Area the anticipated levels of development in these areas will likely be consistent with the continued presence of the purple martin. The historic breeding location of the purple martin at Hemet Lake is not included within the MSHCP Conservation Area, however this site may no longer be viable and may not be active.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The UCR location database includes approximately 15 records for the purple martin within the Plan Area dated from 1908 to 1992. Approximately eight records are relatively recent (within the past 10 years) and of these recent records, four are high precision records that can be accurately placed within the area. The Habitats types associated with these recent and high precision data records include riparian, open water, non-native grassland, and oak woodland which may represent flight observations based on their location. Breeding locations have not been identified within the database but have been identified within the literature and from local experts as discussed below.
The literature available on the purple martin is relatively low. It is focused on the natural history of the species, however, some of the details of its natural history have not been determined. A few general ornithological reference treatments have been prepared for the species and there are some physiological ecology studies that have been conducted.
Habitat and Habitat Associations
Purple martins may be found virtually anywhere in aerial Habitat during migration, including grassland, wet meadow, and fresh emergent wetland, and are usually near water (AOU 1998). The birds typically breed in tall sycamores, pines, and other large trees in or near oak woodlands or open coniferous forest (Garrett and Dunn 1981). The species frequents old-growth, multi-layered, open forest and woodland with snags in the breeding season. It forages over riparian areas, forest, and woodland. The species is an uncommon to rare, local summer resident in a variety of wooded Habitats throughout the state. The species uses valley foothill and montane hardwood, valley foothill and montane hardwood-conifer, and riparian Habitats. It also occurs in coniferous Habitats, including closed-cone pine-cypress, ponderosa pine, Douglas-fir, and redwood. It nests in cavities constructed by other bird species in tall, old trees near a body of water and it also nests occasionally in residential areas. The pre-migratory roost sites are generally situated in stands of trees or underneath concrete bridges (Brown 1997). It is found in a variety of open Habitats in migration (Zeiner et al. 1990).
In western North America, the more northerly populations occur in the Upper Sonoran through the Transition zones. It does not widely use birdhouses in the western portions of the United States but are restricted to areas with dead snags containing woodpecker holes which are generally patchy and local in occurrence. The birds' apparent absence from many potentially suitable areas in the northern Rockies, intermountain region, California, Pacific Northwest, and Mexican highlands may mean that the species has more specific Habitat requirements in these areas that are unknown (Brown 1997).
Biogeography
Purple martins breed locally from British Columbia disjunctly eastward to Nova Scotia southward to Baja California, central Mexico, and the Gulf Coast. Although the species' winter range is not well known, the species primarily winters (presumably) in Amazonia and south-central Brazil. In any case, there are no documented winter records of purple martins for anywhere in North or Central America (AOU 1998).
Zeiner, et al. (1990) summarize the distribution, abundance, and seasonality of the purple martin within California as follows. The purple martin is an uncommon to rare, local summer resident in a variety of wooded Habitats throughout the state. It is a rare migrant in spring and fall and is absent in the winter. In the south, it is now only a rare and local breeder on the coast and in interior mountain ranges, with few breeding localities (Garrett and Dunn 1981). The purple martin is absent from the higher desert regions except as a rare migrant. In the north, it is an uncommon to rare local breeder on the coast and inland (McCaskie, et al. 1979). It is absent from the higher slopes of the Sierra Nevada. The breeding range extends east to Modoc and Lassen counties (Airola 1980). It arrives from South America in late March. The numbers during migration and through the summer remain small. After the young of the year have fledged, flocking begins. Birds of all ages assemble in roosts before the fall departure. Birds in the late-summer roosts generally disperse from the roost site before dawn to forage (Brown 1997). The purple martin departs by late September (Zeiner et al. 1990).
Weather-related mortality periodically eliminates birds along the northern edge of the range, but these areas are usually reoccupied by at least a few individuals within several years. The overall northern limit of the breeding range in Canada has probably shifted southward in the recent century. Installation of birdhouses in the middle and western Great Plains may have permitted a range expansion in recent years. The population along the Pacific Coast is declining (Brown 1997).
Known Populations Within Western Riverside County
The purple martin is currently a rare migrant and breeder in southern California (including the Plan Area) predominantly within the woodlands of the foothill portions of the Plan Area and within the montane areas (Garrett and Dunn 1981). It does not winter within the Plan Area. Observations of the purple martin outside of suitable Habitat are of the species in aerial movement, either foraging or migrating through the area.
Breeding colonies of purple martins apparently persist in the Thomas Mountain and Dripping Springs areas (Patten 1998 pers. comm.). The current status of the breeding colony or colonies reported above Lake Hemet in the San Jacinto Mountains is unknown (Garrett and Dunn 1981). Purple martins have been observed visiting probable nest sites in the Orange County portion of the Santa Ana Mountains very close to the Riverside County line in the late 1980s suggesting the possibility of an additional breeding locale within the Plan Area in the western portion (Gallagher 1997).
Biology
Genetics: All members of genus Progne, of which the purple martin is a member, are closely related and similar in ecology and behavior. Higher-level systematics based on biochemical evidence indicate that Progne martins arose from the hole-excavating swallows in contrast to early speculation that secondary-cavity nesters like Progne were the most primitive hirundinid genera (Sheldon and Winkler 1993).
Diet and Foraging: The diet of the purple martin is composed almost entirely of flying insects (Brown 1997). Types of insects taken varies across the season and probably depends on availability (Brown 1997). Individuals feed most often between 50 and 150 meters above ground (Brown 1997). The purple martin hawks for insects on long, gliding flights 30-60 meters (100-200 feet) above the ground (Airola 1980). Occasionally the purple martin forages on the ground for ants and other insects (Bent 1942). Individuals will forage for insects above water surfaces in ponds and lakes if cold, rainy weather limits the availability of normal food sources (Brown 1997). Usually the purple martin feeds solitarily and does not attempt to feed when air temperature is below about 9oC (Brown 1997). The purple martin drinks while in flight only, by skimming the water surface (Ehrlich, et al. 1988; Brown 1997).
Daily Activity: A study of a purple martin roost site, showed individuals travel a distance of 50-100 meters from the roost site during the day (Russell and Gauthreaux 1998). In a limited nesting season study, eight females spent, on average, 9.23 hours per day flying and 5.78 hours per day sitting at a roosting colony during a total 15 hour period of daylight (Brown 1997).
Reproduction: In the western United States, the purple martin nests in old woodpecker cavities mostly in Habitats within patches of tall sycamores, pines, and other large trees in or near oak woodlands or within open coniferous forests (Garrett and Dunn 1981). The nests may be located in tall, old, isolated trees or snags in open forest or woodland (Zeiner, et al. 1990, Dawson 1923). The western populations of the purple martin nest solitarily in natural or woodpecker-made cavities in trees or cacti (Stutchbury 1991). Cavity-containing trees that have been used as nest sites include pines and aspens, cacti, palms, oaks, sycamores, spruce, firs and cypress. Because the purple martin uses cavities excavated by several different bird species, the cavities that are chosen for nesting differ widely in the size, depth, entrance hole diameter, height above ground, and position within the tree or cactus. For one location in Arizona, the mean cavity height was 7.4 meters above ground (Brown 1997). In eastern North America, nesting may also occur, although less often, in human-made structures, in nesting boxes, under bridges, and in culverts. The use of birdhouses is restricted to the more eastern populations. Purple martins are usually monogamous (Brown 1997).
The purple martin nests from April to August, with peak activity in June. The pair nests colonially or singly, depending on nest site availability. Nest building usually does not begin until several weeks after a pair bond has formed (Brown 1997). A second clutch may be laid, if the first nest fails (Brown 1997). Nest selection occurs by both sexes after a relatively long search (Brown 1997). Nests are built out of twigs and stems of herbaceous plants, leaves and mud (Brown 1997). Individuals may reuse the same nest cavity in successive years (Brown 1997). The mean clutch size has been measured between 4.0 and 4.9 eggs per nest (Brown 1997). The typical range for the clutch size is three to six (Brown 1997). It may raise two broods some years. The altricial young are tended by both parents, and leave the nest at 24-31 days (Harrison 1978). Yearlings can breed but have a reduced success rate and are often found defending cavities with no nests (Brown 1997).
Survival: The maximum life span recorded for the purple martin is 13 years and 9 months in Texas (Brown 1997). Survival rates have been measured at 60.9 percent for adults and 32.2 percent for yearlings (Brown 1997). Purple martins suffer from viral avian pox and various body parasites which may or may not affect reproduction or survivability (Brown 1997; Wagner, et al. 1997). Adverse weather kills more purple martins than all other sources of mortality combined (Brown 1997).
Dispersal: The purple martin is a north-south migrant, following the Central American isthmus between North and South America (Brown 1997). Immediately following fledging, individuals begin to flock before the fall departure (Brown 1997). The young of the year wander widely and relatively few return to the natal colony site. Among banded birds encountered in their first breeding season, 61 percent were found 0 to 1.6 kilometers from their natal nest. Some adults return to the previous year's nest site (Brown 1997).
Socio-Spatial Behavior: Both male and female purple martins will defend a nest site averaging a 20-30 meter radius around the nest (Brown 1997). In Montana, the nest hole entrance was defended by the pair, and the male defended the female while she was foraging away from the nest (Allen and Nice 1952). Nesting colony size is limited by the number of potential nests; the median nearest-neighbor distances in Arizona were between 235 and 325 meters. The purple martin is highly social during the non-breeding season, concentrating in enormous pre-migratory roosts. In some cases, the gregarious nature of communal roosts continues into the nesting season, however, the individuals within the communal roost appear to be non-breeding individuals. During winter roosting, individuals are spaced only five to six centimeters apart (Brown 1997).
Community Relationships: Owls and snakes are probably the most significant predators of both adults and nestlings of this species (Brown 1997). European starlings (Sturnus vulgaris) and house sparrows (Passer domesticus) compete with martins for nest cavities (Brown 1997). Occasionally, native species will nest in martin houses (Brown 1997).
Threats to Species
The purple martin was considered a fairly common summer resident in the early 1930s and had even spread by that time into cities (Willett 1933 in Garrett and Dunn 1981). Numbers of the purple martin have declined markedly in recent decades because of the loss of riparian Habitat, removal of snags, and competition for nest cavities (Remsen 1978). Garrett and Dunn (1981) concluded that the great decline of this species as a breeder in southern California can be linked convincingly to the explosive increase in the regional population of European starlings, which compete with purple martins for nest cavities.
Special Biological Considerations
Unlike tree swallows (Tachycineta bicolor), purple martins apparently have not adapted to artificial nest boxes within southern California (Garrett and Dunn 1981). Thus, attempts to proactively manage the species may be problematic. People provide almost all nesting Habitat, through the use of artificial houses, for the eastern North American purple martin populations (Brown 1997). Artificial houses have helped to augment managed populations in British Colombia, Canada (Brown 1997; Copley, et al. 1999). Local populations can also be aided by trapping and shooting of house sparrows and starlings (Brown 1997).
LITERATURE CITED
AOU (American Ornithologists' Union). 1998. Check-List of North American Birds. Seventh Edition. American Ornithologists' Union, Washington, D.C. 829 pp.
Airola, D. A., ed. 1980. California wildlife Habitat relationships program: Northeast Interior Zone. Vol III. Birds. U.S. Dep. Agric., For. Serv., Lassen Natl. For., Susanville. 590pp.
Allen, R. W., and M. M. Nice. 1952. A study of the breeding biology of the purple martin (Progne subis). Am. Midl. Nat. 47:606-665.
Bent, A. C. 1942. Life histories of North American flycatchers, larks, swallows, and their allies. U.S. Natl. Mus. Bull. 179. 555pp.
Brown, Charles R. 1997. Purple Martin (Progne subis) In The Birds of North America, No. 286 (A. Poole and F. Gills, Eds.) The Academy of Natural Sciences, Philadelphia, PA and The American Ornithologists' Union, Washington, D.C.
Copley, Darren, Dave Fraser and J. Cam. Finlay. 1999. Purple martins (Progne subis): A British Columbia success story. Canadian Field-Naturalist 113: 226-229.
Dawson, 1923. The birds of California. 4 Vols. South Moulton Co., San Diego. 2121 pp.
Ehrlich, P. R., D. S. Dobkin, and D. Wheye. 1988. The birder's handbook. Simon and Schuster, New York. 785pp.
Gallagher, S. 1997. Atlas of Breeding Birds (Orange County, California). Sea and Sage Audubon Press, Santa Ana, California. 264 pp.
Garrett, K. and J. Dunn. 1981. Birds of Southern California: Status and Distribution. Los Angeles Audubon Society. 407 pp.
Harrison, C. 1978. A field guide to the nests, eggs and nestlings of north American birds. W. Collins Sons and Co., Cleveland OH. 416pp.
McCaskie, G., P. De Benedictis, R. Erickson, and J. Morlan. 1979. Birds of northern California, an annotated field list. 2nd ed. Golden Gate Audubon Soc., Berkeley. 84pp.
Patten, Michael. 1998. Riverside County Editor for American Field Notes and Past Secretary, California Bird Records Committee, pers. comm.
Remsen, J. V. Jr. 1978. Bird Species of Special Concern in California. State of California. Department of Fish and Game. Supported by Federal Aid in Wildlife Restoration, Project Pr W-54-R-9, Nongame Wildlife Investigation, Wildlife Management Branch Administrative Report No. 78-1. 54 pp.
Russell, K. R. and S. A. Gauthreaux Jr. 1998. Use of weather radar to characterize movements of roosting purple martins. Wildlife Society Bulletin 26:5-16.
Sheldon, F. H., and D. W. Winkler. 1993. Intergeneric phylogenetic relationships of swallows estimated by DNA-DNA hybridization. Auk 110: 798-824.
Stutchbury, B. J. 1991. Coloniality and breeding biology of purple martins (Progne subis hesperia) in saguaro cacti. Condor 93: 666-675.
Wagner, R. H., P. Davidar, M. D. Schug and E. S. Morton. 1997. Do blood parasites affect paternity, provisioning and mate-guarding in Purple Martins. Condor 99:520-523.
Willett, G. 1933. Revised list of the birds of southwestern California. Pacific Coast Avifauna Number 21.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
sharp-shinned hawk (Accipiter striatus)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
sharp-shinned hawk (Accipiter striatus)
Status:
State: Species of Special Concern
Federal: Partners in Flight Priority Bird Species; San Bernardino National Forest Sensitive
Other: Audubon Society Blue List
GROUP DESIGNATION AND RATIONALE
Group 1
The sharp-shinned hawk has a widespread distribution throughout the MSHCP Plan Area within suitable foraging Habitat. It occurs within the Plan Area as a transient in the spring and fall and may winter within the area. It has not been recorded as breeding within the Plan Area although Habitat is available for that purpose and it has been recorded in the mountainous areas during the summer. It is an opportunistic predator that may forage anywhere within suitable Habitats in the area and has been recorded throughout the entire Plan Area.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 20,500 acres of montane coniferous forest for breeding areas (none have been documented) and 398,280 acres of riparian scrub, woodland, and forest, oak woodland and forest, chaparral, coastal sage scrub, desert scrub, and Riversidean alluvial fan sage scrub for foraging during wintering and transient movements.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
For the purpose of the conservation analysis, potential Habitat for the sharp-shinned hawk includes montane coniferous forest for potential breeding areas (none have been documented) and riparian scrub, woodland, and forest Habitat, oak woodland and forest, chaparral, coastal sage scrub, desert scrub, and Riversidean alluvial fan sage scrub for foraging. Based on these Habitats, the Plan Area supports approximately 659,350 acres of potential Habitat for the sharp-shinned hawk. Table 1 shows the conservation and loss of potential Habitat for the sharp-shinned hawk. Overall, approximately 418,780 acres (64 percent) of potential Habitat in the Plan Area will be conserved in the Criteria Area or existing Public/Quasi-Public Lands.
As described below under Data Characterization, 35 of the 50 relatively recent point localities have a high precision . Of these 35 point localities, 3 (9 percent) will be inside the Criteria Area, 6 (17 percent) are located within public/quasi-public lands and 2 (6 percent) will be in the Rural/ Mountainous areas. Of the 24 high precision recent points located outside the MSHCP Conservation Area, all but four points are located in residential/urban/exotic or agriculture areas and may have been observed in flight due to their observation outside of wooded areas. Providing additional suitable Habitat that is not currently occupied may assist with the conservation of the species. In addition, there are a number of locations that will be conserved that have been documented to be used for wintering and migratory foraging of the sharp-shinned hawk. These areas include: Prado Basin, Santa Ana River, Temescal Wash, Lake Mathews-Estelle Mountain, Wasson Canyon, Sedco Hills, Santa Rosa Plateau, Temecula Creek, Murrieta Creek, Santa Ana Mountains, Vail Lake/Wilson Valley, Tucalota Creek, Lake Skinner/Diamond Valley Lake, Mystic Lake/San Jacinto Wildlife Area, Sycamore Canyon Regional Park, Box Springs, Badlands, and the San Jacinto Mountains.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
SHARP-SHINNED HAWK
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| All Bioregions | |||||||
| Chaparral | 413,470 | 64,900 | 207,370 | 272,270 | 59,580 | 81,620 | 141,200 |
| Coastal Sage Scrub | 152,690 | 47,160 | 34,560 | 81,720 | 26,240 | 44,730 | 70,970 |
| Desert Scrubs | 9,360 | 3,670 | 1,310 | 4,980 | 40 | 4,340 | 4,380 |
| Montane Coniferous Forest | 29,890 | 20 | 20,480 | 20,500 | 40 | 9,350 | 9,390 |
| Riparian Scrub, Woodland, Forest | 14,610 | 3,920 | 7,270 | 11,190 | 370 | 3,050 | 3,420 |
| Riversidean Alluvial Fan Sage Scrub | 7,150 | 3,170 | 2,060 | 5,230 | 220 | 1,700 | 1,920 |
| Oak Woodlands and Forests | 32,180 | 2,390 | 20,500 | 22,890 | 5,020 | 4,270 | 9,290 |
| TOTAL | 659,350 | 125,230 (19%) |
293,550 (45%) |
418,780 (64%) |
91,510 (14%) |
149,060 (22%) |
240,570 (36%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
This species may occur within Forest Service lands for nesting and may also forage during winter movements within montane coniferous woodland, deciduous woodland, and chaparral Habitats. Under the existing Forest Land allocation plan, these locations or Habitats generally are located within the San Jacinto and San Mateo Canyon wilderness areas as well as in most of the grazing allotments. If the Forest Service determines that the sharp-shinned hawk is nesting within the Forest Service lands, core breeding areas should be conserved. Although specific buffer distances have not been determined for this species, due to the similarity to the Cooper's hawk, it is recommended that the Forest Service establish at least a 0.6 kilometer buffer area around any documented sharp-shinned hawk nests.
Conservation of this species should be considered from a landscape perspective because the species is found throughout the Plan Area and may occur in a variety of Habitats. While there are definable locations for focusing conservation efforts, there do not appear to be Core Areas that will be essential for conservation of the species.
MSHCP Conservation Area Configuration Issues
Several large blocks of Habitat supporting or potentially supporting the sharp-shinned hawk will be conserved within the Criteria Area and Public/Quasi-Public lands, including the Prado Basin, Santa Ana River, Lake Mathews-Estelle Mountain, Wasson Canyon, Sedco Hills, Santa Rosa Plateau, Santa Ana Mountains, Vail Lake/Wilson Valley, Lake Skinner/Diamond Valley Lake, Mystic Lake/ San Jacinto Wildlife Area, Sycamore Canyon Regional Park, Box Springs, Badlands, and the San Jacinto Mountains. Other more constrained areas are provided protection by the designation as MSHCP Conservation Area including areas potentially used by the sharp-shinned hawk for foraging such as Temescal Wash, San Timoteo Creek, Temecula Creek, Bautista Creek, and Murrieta Creek. Some of the large blocks of Habitat have not been mapped as containing sharp-shinned hawks possibly due to lack of survey effort or to lack of recording observations. However, these Habitat blocks have potential foraging Habitat and could be occupied by sharp-shinned hawks in the future. As a long-distance migrant and a species with a large foraging area, sharp-shinned hawks are likely able to discover and use patches of Habitat that have not been documented to be used in the past. As such, the MSHCP Conservation Area should provide adequate blocks of a variety of upland and riparian Habitat as Core Areas for this species and should provide large patches of higher elevation Habitat composed of conifer woodlands for potential nesting areas.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 418,780 acres of suitable Conserved Habitat including montane coniferous forest for potential breeding areas and riparian scrub, woodland, and forest Habitat, oak woodland and forest, chaparral, coastal sage scrub, desert scrub, and Riversidean alluvial fan sage scrub for foraging. The MSHCP Conservation Area includes preservation of large blocks of areas that contain a variety of potentially suitable Habitat for foraging use during winter and migration as well as very large blocks that contain potentially suitable nesting Habitat.
INCIDENTAL TAKE
About 240,570 acres (about 36 percent) of potential Habitat for the sharp-shinned hawk will be outside the Criteria Area and Public/Quasi-Public designations, and individuals within these areas will be subject to Incidental Take consistent with the Plan. Of this, approximately 91,510 acres of potential Habitat (14 percent) are located within Rural/Mountainous designation areas. While the Rural/Mountainous areas are not included within the MSHCP Conservation Area and will not be managed for the benefit of wildlife, the anticipated levels of development areas will likely be consistent with maintaining some Habitat for the sharp-shinned hawk.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature. The UCR location database for the sharp-shinned hawk includes a total of 100 records dated from 1900 to 2000. Approximately 50 of these records are recent (within the past 10 years) and of these, a total of 35 records are of high precision. These recent high precision records are located within residential, agriculture, chaparral, grassland, sage scrub, riparian, oak woodland and a variety of other Habitats. Most of the records reflect the transient locations due to the season or Habitat within which the observation took place. Even those recorded for residential Habitat could be extant and were likely observations of a bird flying or hunting overhead. Only four records are located in montane forest and are potential breeding locations. No documented breeding locations are present within the database.
There is a moderate amount of literature available for the sharp-shinned hawk due to its inclusion with the birds of prey and thus high interest within the ornithological field. Most studies are focused on general Habitat, breeding, and natural history studies and a number of them focus on the relation of the sharp-shinned hawk to its congeners due to the potential for competition. Few studies are available for the Plan Area other than general distribution information for the region.
Habitat and Habitat Associations
The species breeds in young coniferous forests with high canopy associations. Habitats that they are documented to use include ponderosa pine, black oak, riparian deciduous, mixed conifer, and Jeffrey pine. The species uses dense stands in close proximity to open areas. It roosts in intermediate to high-canopy forest and nests in dense, even-aged, single-layered forest canopy. Usually it is found in large remote woods throughout most of the continent (Terres 1980). Although they seem to prefer riparian Habitats they are not restricted to them and are found in mid-elevation Habitat such as pine forests, woodlands and mixed conifer forests and appear to nest in forested areas particularly with some conifers (Bildstein and Meyer 2000). For nesting they occur in dense tree stands which are cool, moist, well shaded and usually near water. For hunting Habitat, they often use openings at the edges of woodlands and also brushy pastures (USFS pers. comm. 1999).
Sharp-shinned hawks may occur in a large variety of woodland Habitats during winter and migration periods and are most common in southern California in the coastal lowlands and desert areas (Garrett and Dunn 1981). The species winters in woodlands and other Habitats except alpine, open prairie and bare desert (Zeiner, et al. 1990). The female sharp-shinned hawk uses continuous deciduous forest and small dense pine stands within deciduous areas for wintering. The males use mixed forest and transitional Habitat near open areas and ecotonal Habitats, where densities of potential prey species are higher for wintering periods (Bildstein and Meyer 2000).
Biogeography
The sharp-shinned hawk breeds from Alaska southward throughout much of Canada, the northern portions of the lower 48 states, the Rocky Mountains and mountains of the far west, parts of the Gulf States, and the highlands of Mexico. The range of the sharp-shinned hawk for nesting is from northwestern Alaska, Yukon, northern Saskachewan, central Manitoba, northern Ontario, central Quebec, Newfoundland, south to California, Mexico, Texas, Louisiana, Tennessee, South Carolina, and Alabama (Terres 1980).
A highly migratory species, the sharp-shinned hawk winters from the lower 48 states to Panama and various Caribbean islands (AOU 1998). Specifically, it winters from Vancouver Island, southern British Columbia, western Montana, Nebraska, southern Minnesota, Illinois, southern Michigan, southern Ontario, New York, and Nova Scotia south to Panama and the Bahamas (Terres 1980).
In California, the sharp-shinned hawk is a fairly common migrant and winter resident throughout except in areas with deep snow. Breeding distribution of the species is poorly documented. There are very few breeding records for the Cascades/Sierra Nevada. It probably breeds south in the Coast Ranges to about 35 degrees latitude, and at scattered locations in the Transverse and Peninsular Ranges. It may no longer breed in the southern Sierra Nevada. It is an uncommon winter migrant to the Channel Islands. It is an uncommon permanent resident and breeder in mid-elevation Habitats using ponderosa pine, black oak, riparian deciduous, mixed conifer, and Jeffrey pine Habitats for breeding within its range (Zeiner, et al. 1990). Small (1994) describes the range of the sharp-shinned hawk in California as poorly known. Breeding or summering birds have occurred throughout California, including the southern mountains, but Small (1994) indicates the it most probably breeds only in the northern half of the state.
There is little data for historical range of the sharp-shinned hawk. It is likely that the dependence of this species on relatively large tracts of contiguous forest for nesting, at least until recently, has affected the distribution particularly in eastern North America where local and regional distributions shifted in responses to the widespread loss of the eastern deciduous forest. Currently there appears to be an expansion in the sharp-shinned hawks breeding range southward continent-wide (Bildstein and Meyer 2000).
Known Populations Within Western Riverside County
Although sharp-shinned hawks have been repeatedly recorded in the San Jacinto Mountains during summer months, there are no confirmed records of breeding there or in the Plan Area as a whole (Grinnell and Miller 1944; Garrett and Dunn 1981). Based on Small (1994), it is likely the sharp-shinned hawk occurs within southern California mountainous areas as a summering bird and not a breeder. The species is, however, a fairly common migrant and wintering species within southern California and much of the Plan Area.
The sharp-shinned hawk has been recorded predominantly within the western and central portion of the Plan Area within a large variety of Habitats. Locations recorded within the U.C. Riverside database include only migrant and wintering observations for: Alberhill, Banning, El Cerrito, Homeland/Lakeview Mountains, Rubidoux, Santa Rosa Plateau West, Sun City, Motte-Rimrock Reserve, Woodcrest, Santa Ana River, Lake Mathews Reserve, Lake Perris SRA, San Jacinto Wildlife Area, Prado Basin, Temescal Wash, Railroad Canyon, Sedco Hills, Temecula Creek, Murrieta Creek, Santa Ana Mountains, Vail Lake/Wilson Valley, Tucalota Creek, Lake Skinner-Diamond Valley Lake, Box Springs, Badlands, and the San Jacinto Mountains.
Biology
Genetics: Ten subspecies of the sharp-shinned hawk are recognized. These are divided into three subspecies groups by the American Ornithological Union (1998): sharp-shinned hawk (striatus group), white-breasted hawk (chionogaster group), and rufous-thighed hawk (erythronemius group).
Diet and Foraging: The sharp-shinned hawk feeds almost entirely on small birds, usually no larger than jays; it also rarely takes small mammals, insects, reptiles, and amphibians (Brown and Amadon 1968). It perches, and darts out in sudden flight to surprise its prey; it also cruises rapidly in search flights. Often the sharp-shinned hawk hunts as a harrier, in low, gliding flights. It often forages in openings at edges of woodlands, hedgerows, brushy pastures, and shorelines, especially where migrating birds are found (Zeiner, et al. 1990). North-facing slopes with prey plucking perches are a critical Habitat requirement. These hawks choose avian prey opportunistically (Joy et al. 1994). Throughout the range, sexes of wintering sharp-shinned hawks differ in the use of Habitats for foraging with females in continuous deciduous forest and males in smaller patches of mixed forest and transitional Habitats (Meyer 1987).
Daily Activity: The sharp-shinned hawk exhibits year-long, diurnal activity (Zeiner et al. 1990). In a study in Utah, the breeding male spent little time at the nest and most of the day in hunting areas. Hunting begins in early morning, typically within 5 minutes of waking (Platt 1973). In some locations the species soars daily, especially in the morning or late afternoon.
Reproduction: The average distance between nests of the sharp-shinned hawk is 2.5 miles (Zeiner, et al. 1990). The species usually nests in dense, pole and small-tree stands of conifers which are cool, moist, well shaded, with little groundcover and near water (Call 1978). The sharp-shinned hawk tends to nest in forest stands with a greater percent cover of conifer trees than the Cooper's hawk and also tends to place the nest within the canopy of the tree (Trexel, et al. 1999; Wiggers and Kritz 1991). The sharp-shinned hawk uses many species of trees for the nest tree, typically within relatively dense stands. Conifers are the tree most frequently used for the nest site, although in some locations, deciduous trees are used predominantly (Bildstein and Meyer 2000). The nests may be reused in later years (Reynolds, et al. 1982). The nest of the sharp-shinned hawk is a platform or cup in dense foliage against the trunk, or in the main crotch of a tree, usually 2-24 meters (6-80 feet) above ground. This species has the most inconspicuous nest of the accipiters (Call 1978).
The nesting season for the sharp-shinned hawk in Missouri was recorded from May to August (Wiggers and Kritz 1994). It breeds from April through August in California, with the peak nesting period from late May to July (Zeiner et al. 1990). The clutch averages 4-5 eggs, with a range of 3-8. Incubation is 34-35 days and is done by both parents. The male brings food to the female and the semi-altricial young; fledging occurs at about 60 days. Among 11 pairs in Oregon, Reynolds (1975) reported 2.7 young/ pair, and a hatching success of 70 percent. Egg loss in the species was greater than nestling loss. Females generally breed at one year and all breed by the second year (Bildstein and Meyer 2000).
Survival: The longest lifespan of the sharp-shinned hawk is 13 years (Keran 1981). No rigorous analysis of survival is available. Based on 92 band recoveries, 19 percent were from one year, 24 percent were from two years, 25 percent were from three years, 15 percent were from four years, 10 percent were from five years, 5 percent were from six years, 2 percent were from seven years, and 2 percent were from eight years of age (Bildstein and Meyer 2000).
Dispersal: The young of the sharp-shinned hawk first fly about 23 days after hatching (Brown and Amadon 1968). One fledgling that was radio-tagged in Utah remained in the nest grove until the fourth week after fledging. It then left the area and was not relocated. There appears to be a sudden departure of the young of the year with no subsequent detections in the nest area (Bildstein and Meyer 2000).
Socio-Spatial Behavior: In Wyoming, Craighead and Craighead (1956) measured two breeding home ranges of 67 hectares and 132 hectares (166 and 326 acres). Reynolds (1979) reported crude home range sizes of 2,750 hectares (6,600 acres). The territory appears to be the same as the home range. Distances averaged 4.1 kilometers (2.5 miles) between nests. The sharp-shinned hawk demonstrates very active nest defense and resident males will fly straight at and chase approaching intruders. Breeding home ranges may be as large as approximately 800 hectares (Johnsgard 1990).
Community Relationships: Fledging is timed to coincide with the fledging of prey birds, providing a food supply for young, inexperienced hunters (Reynolds, et al. 1982). The sharp-shinned hawk is an important predator of small birds. It may compete with the Cooper's hawk (Reynolds 1975, 1979).
Threats to Species
Although no longer considered vermin, sharp-shinned hawks are still being shot in Latin American wintering grounds (Johnsgard 1990).
Sharp-shinned hawks probably declined at one point from pesticide effects as seen in egg shell thinning which were likely picked up in the breeding range. The populations had experienced a steady decline from the early 1950s through the early 1960s and had stabilized by the mid-1960s and increased to near early 1950s levels by the late 1960s (Remsen 1978). However, sharp-shinned hawks are still showing negative affected by exposure to pesticides and still appear to have relatively high levels of organochlorine pesticides which they may be picking up in neotropical areas (Henny 1987; Reynolds 1989).
The total population breeding within California is very small, and thus vulnerable to impact from falconry, although at present this species is not taken by falconers to a significant extent.
Logging and timber harvest is another potential hazard (Remsen 1978, Reynolds 1989). However, the lack of accurate estimates of the abundance at any level precludes assessment of the population-level effects of forest management practices and Habitat degradation due to agricultural and urban development in North America. The loss of Neotropical forests may be important to the prey species which may have caused declines in the sharp-shinned hawk at the migration watch sites (Bildstein and Meyer 2000).
Special Biological Considerations
Although sharp-shinned hawks apparently demonstrate significant site fidelity in the short-term, pairs do not occupy a particular site for more than two consecutive years (Jones 1979). North-facing slopes with prey plucking perches are a critical Habitat requirement for breeding locations (Zeiner, et al. 1990).
The sharp-shinned hawk formerly bred in small numbers throughout much of northern California and in very small numbers in all the mountain ranges of southern California as far south as the Cuyamaca Mountains (Grinnell and Miller 1944). The breeding population appears greatly reduced from former levels, but data are lacking. Only a few individuals are reported during the summer months, and almost all of these are from northern California (Small 1994).
LITERATURE CITED
AOU (American Ornithologists' Union). 1998. Check-List of North American Birds. Seventh Edition. American Ornithologists' Union, Washington, D.C. 829 pp.
Bildstein, Keith L. And Ken Meyer. 2000. Sharp-shinned Hawk (Accipiter striatus), No. 482. In The Birds of North America. A. Poole and F. Gill, Eds. Cornell Laboratory of Ornithology and the Academy of Natural Sciences, Washington D.C.
Brown, L., and D. Amadon. 1968. Eagles, hawks and falcons of the world. 2 Vols. Country Life Books, London. 945pp.
Call, M.W. 1978. Nesting habits and survey techniques for common western raptors. U.S. Dept. Interior Bureau of Land Management. Portland Oregon. Technical Note No 316. 115 pp.
Craighead, J. J., and F. C. Craighead, Jr. 1956. Hawks, owls and wildlife. Stackpole Books, Harrisburg, PA. 443pp.
Garrett, K. and J. Dunn. 1981. Birds of Southern California: Status and Distribution. Los Angeles Audubon Society. 407 pp.
Grinnell, J. and A.H. Miller. 1944. The Distribution of the Birds of California. Pacific Coast Avifauna Number 27. Copper Ornithological Club, Berkeley, California. Reprinted by Artemisia Press, Lee Vining, California; April, 1986. 617 pp.
Henny, C. J. 1987. Birds of prey, DDT, and tussock moth in the Northwest. Trans. Am. Wildl.Nat. Res. Conf. 42: 397-411.
Johnsgard, P. A. 1990. Hawks, Eagles, and Falcons of North American. Smithsonian Inst. Press, Washington, D. C. 403pp.
Jones, S. 1979. Habitat management series for unique or endangered species. Report No. 17: the Accipiters: goshawk, Cooper's hawk, sharp-shinned hawk. USDOI, Bureau of Land Management Technical Notes 335. 51pp.
Joy, S. M, R.T. Reynolds, R. L. Knight and R. W. Hoffman. 1994. Feeding ecology of sharp-shinned hawks nesting in deciduous and coniferous forests in Colorado. Condor 96: 455-467.
Keran, D. 1981. The incidence of man-caused and natural mortalities in raptors. J. Raptor Research 15: 108-112.
Meyer, K. D. 1987. Sexual size dimorphism and the behavioral ecology of breeding and wintering sharp-shinned hawks. Chat 46: 78-80.
Platt, J. B. 1973. Habitat and time utilization of a pair of nesting sharp-shinned hawks - a telemetry study. Master's thesis, Brigham Young University, Provo.
Remsen, J. V., Jr. 1978. Bird species of special concern in California. Calif. Dep. Fish and Game, Sacramento. Wildl. Manage. Admin. Rep. No. 78-1. 54pp.
Reynolds, R. T. 1975. Distribution, density, and productivity of three species of Accipiter hawks in Oregon. M.S. Thesis, Oregon State Univ., Corvallis. 39pp.
Reynolds, R. T. 1979. Food and Habitat partitioning in two groups of coexisting Accipiters. Ph.D. Diss., Oregon State Univ., Corvallis. 116pp.
Reynolds, R. T., E. C. Meslow, and H. M. Wight. 1982. Nesting Habitat of coexisting Accipiters in Oregon. J. Wildl. Manage. 46:124-138.
Reynolds, R. T. 1989. Accipiters. Pages 92-101 in National Wildlife Federation Proceedings of Western Raptor Management Symposium and Workshop. National Wildlife Federation Technical Series Number 12. 317pp.
Small, A. 1974. The Birds of California. Macmillan Publishing Co. New York. 310 pp.
Terres, J. K. 1980. The Audubon Society Encyclopedia of North American Birds. Alfred A. Knopf, New York, New York. 1109pp.
Trexel, D. R., R. N. Rosenfield, J. Bielefeldt, and E. A. Jacobs. 1999. Comparative nest site Habitats in sharp-shinned and Cooper's hawks in Wisconsin. Wilson Bulletin 111: 7-14.
United States Forest Service (USFS). 1999. Pers. comm. Species accounts for threatened, endangered and sensitive wildlife species occurring in the San Bernardino National Forest.
Wiggers, E. P. and K. J. Kritz. 1994. Productivity and nesting chronology of the Cooper's hawk and sharp-shinned hawk in Missouri. Journal of Raptor Research 28:1-3.
Wiggers, E. P., and K. J. Kritz. 1991. Comparison of nesting Habitat of coexisting sharp-shinned and Cooper's hawks in Missouri. Wilson Bulletin. 103: 568-577.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
Southern California rufous-crowned sparrow (Aimophila ruficeps canescens)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
Southern California rufous-crowned sparrow (Aimophila ruficeps canescens)
Status:
State: Species of Special Concern
Federal: Federal Special Concern species;
Other: Audubon Society California Watch List
GROUP DESIGNATION AND RATIONALE
Group 2
The Southern California rufous-crowned sparrow is widely distributed throughout the MSHCP Plan Area within suitable Habitat in the Riverside Lowlands, Santa Ana Mountains, and San Jacinto Foothills Bioregions. It is absent from higher elevation Bioregions and the Desert Transition Bioregion. The Southern California rufous-crowned sparrow occurs within several Core Areas including Lake Mathews-Estelle Mountain, Gavilan Plateau, Box Springs Mountains, Lake Perris, Badlands, west of Lake Elsinore, Wasson Canyon, Santa Rosa Plateau, Lake Skinner, De Portola Road east of Bachelor Mountain, Wilson Valley, and the Hogbacks. The Southern California rufous-crowned sparrow is a year-round resident but may make movements to lower elevations for the winter. Because rufous-crowned sparrow Habitat requirements are well known, the species occurs widely within these Habitats in the Riverside lowlands, San Jacinto Foothills, and Santa Ana Mountains Bioregions, and specific Core Areas exist for the species, it is anticipated that Southern California rufous-crowned sparrow will respond well to a landscape level of management with site specific requirements.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 82,640 acres of suitable primary Habitat for the Southern California rufous-crowned sparrow including coastal sage scrub, Riversidean alluvial fan sage scrub, and desert scrubs in Riverside Lowland, Santa Ana Mountains, and San Jacinto Foothills Bioregions.
Objective 2
Include within the MSHCP Conservation Area at least 9 Core Areas and interconnecting linkages. Core areas will include: Lake Mathews-Estelle Mountain (Existing Core C plus Proposed Extension of Existing Core 2; 23,710 acres), Box Springs Mountains (Existing Noncontiguous Habitat Block A plus Proposed Constrained Linkage 8; 2,920 acres), Lake Perris (Existing Core H; 17,470 acres), the Badlands (Proposed Core 3; 24,920 acres), west of Lake Elsinore (represented by Existing Core B; 71,490 acres), Wasson Canyon (Subunit 5 of Elsinore Area Plan; 2,320 acres), Lake Skinner (including Diamond Valley Lake; Existing Core C plus Proposed Extension of Existing Cores 5, 6, 7; 29,060 acres), Wilson Valley (Subunit 2 of REMAP Area Plan; 33,540 acres), and the Hogbacks (Proposed Core 2; 5,050 acres).
Objective 3
Include within the MSHCP Conservation Area at least 174,620 acres of suitable secondary Habitats for the Southern California rufous-crowned sparrow including chaparral and grasslands in Riverside Lowland, Santa Ana Mountains, and San Jacinto Foothills Bioregions.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
Although the distribution and Habitat of the Southern California rufous-crowned sparrow are very similar to that of the California gnatcatcher, the Southern California rufous-crowned sparrow appears to occur at higher elevations, in a more scattered distribution throughout the MSHCP Plan Area, and more often in non-coastal sage scrub Habitats such as grassland and chaparral, especially on hilly slopes with rock outcrops or on edges of denser scrub and chaparral associations. Thus, the conservation analysis for Southern California rufous-crowned sparrow includes more Habitat types and includes the higher elevations within the Santa Ana Mountains Bioregions within which they have been recorded. For the purpose of the conservation analysis, primary Habitat includes coastal sage scrub, Riversidean alluvial fan sage scrub, and desert scrubs within the Riverside lowlands, Santa Ana Mountains, and San Jacinto Foothills Bioregions. Secondary Habitat includes chaparral and grassland within the Riverside lowlands, Santa Ana Mountains, and San Jacinto Foothills Bioregions. Based on these Habitats, the Plan Area supports approximately 503,250 acres of Habitat for the Southern California rufous-crowned sparrow comprised of 153,620 acres of primary Habitat and 349,630 acres of secondary Habitat,. Table 1 shows the conservation and loss of Habitat for the Southern California rufous-crowned sparrow. Overall, approximately 82,640 acres (54 percent) of potential primary Habitat and 174,620 acres (50 percent) of potential secondary Habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public Lands.
This species may nest and forage within coastal sage scrub, grasslands, and chaparral along the eastern foothills of the Santa Ana Mountains within the Cleveland National Forest. Under the existing Forest Land Allocation plan, these locations or Habitats generally are located within the Wildhorse roadless area and areas east and at lower elevations. They may also be present within the San Mateo Canyon Wilderness Area and possibly the Tenaja, El Cariso, and Verdugo Range Allotments although no information on occurrence is available for these areas.
As described below under Data Characterization, 149 of 400 point localities have a high location precision. Of these 149 point localities, 50 (34 percent) will be inside the Criteria Area or Public/Quasi-Public lands. A total of 33 (22 percent) will be in the Rural/Mountainous zone. Of the 66 (44 percent) points located outside these designations, 32 are mapped in existing residential/ urban/exotic areas and may no longer be extant. Conservation of this species will be considered from a landscape perspective because the species is found throughout the Plan Area in defined Habitat associations. The landscape analysis will focus on conservation of Core Areas and connective Habitat between these areas.
As indicated above, conservation efforts will focus on 9 of 12 Core Areas of the Southern California rufous-crowned sparrow. These areas include Lake Mathews-Estelle Mountain (Existing Core C plus Proposed Extension of Existing Core 2; 23,710 acres), Box Springs Mountains (Existing Noncontiguous Habitat Block A plus Proposed Constrained Linkage 8; 2,920 acres), Lake Perris Existing Core H; 17,470 acres), the Badlands (proposed Core 3; 24,920 acres), west of Lake Elsinore (represented by Existing Core B; 71,490 acres), Wasson Canyon (Subunit 5 of Elsinore Area Plan; 2,320 acres), Lake Skinner (including Diamond Valley Lake; Existing Core C plus Proposed Extension of Existing Cores 5, 6, 7; 29,060 acres), Wilson Valley (Subunit 2 of REMAP Area Plan; 33,540 acres), and the Hogbacks (Proposed Core 2; 5,050 acres). The total acreage of Core Areas within Criteria Area and Public/Quasi-Public lands is 207,480 acres. These Core Areas will be connected as well. Some additional locations of the Southern California rufous-crowned sparrows will be conserved within the Jurupa Mountains, Chino Hills, Sycamore Canyon Regional Park, Lakeview Mountains, North Peak Conservation Bank, Kabian Park, Sedco Hills, and Vail Lake.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
SOUTHERN CALIFORNIA RUFOUS-CROWNED SPARROW
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| Primary Habitat in Riverside Lowlands, San Jacinto Foothills, and Santa Ana Mountains Bioregions | |||||||
| Desert Scrubs | 2,230 | 2,160 | 0 | 2,160 | 40 | 30 | 70 |
| Riversidean Alluvial Fan Sage Scrub | 5,770 | 2,850 | 1,380 | 4,230 | 190 | 1,350 | 1,540 |
| Coastal Sage Scrub | 145,620 | 44,040 | 32,210 | 76,250 | 25,970 | 43,400 | 69,370 |
| Subtotal Primary Habitats | 153,620 | 49,050 (32%) |
33,590 (22%) |
82640 (54%) |
26,200 (17%) |
44,780 (29%) |
70,980 (46%) |
| Secondary Habitat in Riverside Lowland, San Jacinto Foothills, and Santa Ana Mountains Bioregions | |||||||
| Grassland | 132,040 | 18,220 | 20,470 | 38,690 | 11,330 | 82,020 | 93,350 |
| Chaparral | 217,590 | 49,280 | 86,650 | 135,930 | 47,350 | 34,310 | 81,660 |
| Subtotal Secondary Habitats | 349,630 | 67,500 (19%) |
107,120 (31%) |
174,620 (50%) |
58,680 (17%) |
116,330 (33%) |
175,010 (50%) |
| TOTAL | 503,250 | 116,550 (23%) |
140,710 (28%) |
257,260 (51%) |
84,880 (17%) |
161,110 (32%) |
245,990 (49%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
MSHCP Conservation Area Configuration Issues
Several large blocks of Habitat supporting the Southern California rufous-crowned sparrow will be conserved within Criteria Area and Public/Quasi-Public designations, including the Core Areas at Lake Mathews-Estelle Mountain, Box Springs Mountains, Lake Perris, the Badlands, west of Lake Elsinore, Wasson Canyon, Lake Skinner, Wilson Valley, and the Hogbacks. Other locations with moderate numbers that will be conserved include Jurupa Mountains, Chino Hills, Sycamore Canyon Regional Park, Motte-Rimrock Reserve, Lakeview Mountains, North Peak Conservation Bank, Kabian Park, Sedco Hills, and Vail Lake.
Areas that are important for preservation for dispersal purposes between the Plan Area and other areas, but that may not contain large numbers of Southern California rufous-crowned sparrows, include the Jurupa Mountains for connectivity to San Bernardino County, Chino Hills for connectivity to Orange County, Santa Margarita Ecological Reserve and eastern Temecula Creek for connectivity to San Diego County.
The Southern California rufous-crowned sparrow is a year-round resident and may not be as adept at dispersing as some of the long distance migrant bird species. No data are available specific to the Southern California rufous-crowned sparrow, but the literature recommends protecting large interconnected blocks of coastal sage scrub Habitat. As such, the MSHCP Conservation Area will provide Habitat linkages between the preserved Core Areas for this species. The large block of Habitat within the Core Area at Lake Mathews-Estelle Mountain Reserve is connected to the Wasson Canyon Core Area along Temescal Wash and the hillsides east of the wash with a wide linkage at a 2,000 foot minimum width. Connections to the eastern foothills of the Santa Ana Mountains and the west of the Lake Elsinore Core Area are located at several drainages including Indian Canyon and Horsethief Canyon. The Core Area and locations within the Santa Ana Mountains and Santa Rosa Plateau Nature Reserve are connected within the Cleveland National Forest lands and by the Tenaja corridor.
The Wasson Canyon Core Area is connected to the Hogbacks area along the Sedco Hills through Wildomar to the Hogbacks, and to the Lake Skinner Core Area via the AD161 mitigation area and a number of Proposed Constrained Linkages. The Lake Skinner Core Area is linked to the Wilson Valley area by the Tucalota Valley linkage and the Proposed Linkage through Cactus Valley. The Cactus Valley area is a large block of Habitat connecting the Lake Skinner/Diamond Valley Lake area east to the San Bernardino National Forest and along Bautista Creek and the Upper San Jacinto River to the large block of Habitat within the Badlands. The block of Habitat within the Lake Perris Core Area is connected to the Badlands along the San Jacinto River and Lamb Canyon.
The MSHCP Conservation Area design for the Southern California rufous-crowned sparrow needs to take into account that large scale fires damage Habitat for a relatively long length of time. Complicating this is that fire may assist with providing additional suitable Habitat for the Southern California rufous-crowned sparrow. Fire management will be an important factor in addressing the conservation of this species. Large areas will be necessary to provide refugia for birds and to supply dispersing individuals to a recovering area. Duplicate linkages also provide for the temporary loss of function of the coastal sage scrub Habitat in the event of a fire. A duplicity of Habitat linkages composed of sage scrub and other undeveloped Habitats may provide for dispersal. Several duplicate linkages are preserved in the MSHCP Plan Area including linkages along the Santa Ana Mountains foothills within the Interstate 15 corridor and between the Lake Skinner/Diamond Valley Lake area and the Hogbacks.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 82,640 acres of suitable primary Conserved Habitat and 174,620 acres of suitable secondary Conserved Habitat and 9 of 12 Core Areas within large blocks of Habitat in the MSHCP Conservation Area. In addition, 50 recent and high precision locations will be inside the Criteria Area or Public/Quasi-Public lands, all of which are recorded for the suitable Habitat of the Southern California rufous-crowned sparrow. Conservation also will be provided for the Habitat linkages between Core Areas and areas important for dispersal as described above. The current population size of the Southern California rufous-crowned sparrow is unknown, however the species is well documented as to the Habitat that it uses and locations that constitute Core Areas.
INCIDENTAL TAKE
The Incidental Take of the Southern California rufous-crowned sparrow is difficult to quantify due to our limited knowledge of its distribution and abundance within the Plan Area. The maximum level of Incidental Take of Southern California rufous-crowned sparrows can be anticipated by the loss of the number of acres of potential Habitat that will become unsuitable for this species. About 70,980 acres of potential primary Habitat for the Southern California rufous-crowned sparrow will be outside the Criteria Area and Public/Quasi-Public designations, or about 46 percent of the total potential primary Habitat. Approximately 175,010 acres of secondary Habitat for the Southern California rufous-crowned sparrow will be outside the MSHCP Conservation Area, about 50 percent of the potential secondary Habitat. Individuals within these areas are subject to Incidental Take consistent with the Plan. Of this, approximately 26,200 acres (17 percent) of potential primary Habitat and 58,680 acres (17 percent) of potential secondary Habitat are located within Rural/ Mountainous designation areas. Core Areas not conserved within Criteria Area and Public/Quasi-Public designations include the Gavilan Plateau, Santa Rosa Plateau, and De Portola Road east of Bachelor Mountain. A total of 33 (22 percent) of the recent and high precision locations will be in the Rural/Mountainous zone and 66 (44 percent) are outside the MSHCP Conservation Area. Of the 66 points located outside the MSHCP Conservation Area, 32 are mapped in existing residential/ urban/exotic areas and may no longer be extant.
SPECIES ACCOUNT
Data Characterization
The UCR location database for the Southern California rufous-crowned sparrow includes approximately 487 records dated from 1900 to 1999. Approximately 400 of these are recent records (within the past 10 years) and approximately 149 of these are high precision records. The Habitat types for these recent high precision records include predominantly sage scrub, chaparral and grassland. A number of the recent high precision records, approximately 37, are recorded for residential areas or agriculture and are either located adjacent to the residential development or crop lands or no longer exist.
There is a low amount of literature available for the Southern California rufous-crowned sparrow. Most of this is general and relatively old descriptive literature documenting general and anecdotal natural history and distribution of the species. Very little information is available for the species within the Plan Area other than distribution information within the region as a whole.
Habitat and Habitat Associations
Southern California rufous-crowned sparrows are found on moderate to steep, dry, grass-covered hillsides, coastal sage scrub, and chaparral and often occur near the edges of the denser scrub and chaparral associations. Preference is shown for tracts of California sagebrush (Artemisia californica) (Collins 1999). It also colonizes grass that grows as a successional stage following brush fires and sparse chaparral recovering from a burn as well as the edges of tall chaparral (Unitt 1984, Collins 1999). Optimal Habitat consists of sparse, low brush or grass, hilly slopes preferably interspersed with boulders and outcrops (Willet, 1912, 1933; Grinnell 1915, 1926, Grinnell and Miller 1944; Bent 1968; Pulliam and Mills 1977; Phillips, et al. 1983; Unitt 1984; Ehrlich, et al. 1988; Root 1988). The species may occur on steep grassy slopes without shrubs if rock outcrops are present (Zeiner et al. 1990). Some observers have noted a preference for south-facing or west-facing slopes and an affinity for California sagebrush over other vegetative types (Barlow 1902, Grinnell 1915, Grinnell and Miller 1944, Bent 1968; Root 1988). It is uncommon on the lower slopes of the western Sierra Nevada, and on Santa Cruz Island (Grinnell and Miller 1944). It is most numerous in the western portion of its range in California (Zeiner et al. 1990).
The Southern California rufous-crowned sparrow is a very secretive species. It seeks cover in shrubs, rocks, and grass and forb patches. It is frequently found in open shrubland in valley foothill hardwood-conifer savannah and open chaparral (Verner and Boss 1980). It is generally absent from dense, unbroken stands of coastal sage scrub and chaparral. The elevation range in California has been recorded as 60 to 1,400 meters (Collins 1999).
The physical and vegetative characteristics of the Southern California rufous-crowned sparrow have been quantified by Collins (1999). The results have confirmed that this species prefers moderate west, south-, and east-facing slopes vegetated with low, fairly open cover of shrubs and grass. Most of the inhabited sites (89 percent) were on slopes of 15 to 60 degrees. Almost half of the sites were on moderate slopes (30 to 45 degrees). Rock outcrops were present at 61 percent of the occupied sites. Shrub and grass were the dominant cover types with shrubs averaging 50 percent cover and grass averaging 29 percent. Shrub height was generally low in this study, averaging 0.83 meters. The dominant overstory shrubs associated with the Habitats used by this species include California sagebrush, purple sage (Salvia leucophylla), black sage (S. mellifera), California encelia (Encelia californica), coyote brush (Baccharis pilularis), mock heather (Ericameria ericoides), deer weed (Lotus scoparius), giant rye (Leymus condensatus), and buckwheat (Eriogonum sp.).
Biogeography
The rufous-crowned sparrow, including all subspecies, is largely a resident species and occurs in central California, north-central Arizona, southwestern New Mexico, southeastern Colorado, northwestern and central Oklahoma, south discontinuously to southern Baja California and Mexico. The species occurs throughout much of the southwestern United States and Mexico but the range is often discontinuous with numerous small, isolated populations (Collins 1999). East of the Rocky Mountains, it winters from central and southern Oklahoma to northern Texas and south into Mexico (Terres 1980).
The current range and distribution of the Southern California rufous-crowned sparrow subspecies is extremely restricted to a narrow belt of semiarid coastal sage scrub and sparse chaparral from Santa Barbara south to the northwestern corner of Baja California. (Todd, 1922, Grinnell, 1926, Grinnell and Miller 1944, Bent 1968, Zeiner, et al. 1990; Unitt 1984). It is generally resident throughout its range, and no true migratory movements have been recorded. Limited movements to lower elevations have been reported during especially severe winters (Collins 1999).
The conversion of large areas of coastal sage scrub for urban and agricultural developments have made this species more locally restricted in various southern California counties (Los Angeles, Orange, Riverside, San Diego, and San Bernardino counties) (Collins 1999).
Known Populations Within Western Riverside County
The UCR database locations indicate the majority of reported occurrences of Southern California rufous-crowned sparrows are in the southwestern corner and central portion of the Plan Area, forming a broad band between Interstate 15 and 215 from the northern end of the Plan Area to the southern end between Temecula and Lake Skinner area. The database locations are more sparsely scattered east of this broad band to and including the Badlands and south into the Sage and Aguanga areas.
Although difficult to assign Core Areas to the broad scatter of database locations some trends or clusters of locations appear to include the areas in the vicinity of Lake Mathews-Estelle Mountain, Gavilan Plateau, Box Springs Mountains, Lake Perris, Badlands, west of Lake Elsinore, Wasson Canyon, Santa Rosa Plateau, Lake Skinner, De Portola Road east of Bachelor Mountain, Wilson Valley, and the Hogbacks.
Biology
Genetics: The rufous-crowned sparrow has been placed in several different genera depending on the past nomenclatural and taxonomic conventions and decisions: e.g., Ammodramus, Zonotrichia, Peucaea, and Aimophila, where it is currently assigned ( Collins 1999). The Southern California rufous-crowned sparrow is similar to the nominate ruficeps, except the wing and tail are longer, the bill is smaller, the underparts brown with a grayish wash, and the upper parts are rufous-brown with a grayish-buff streaking (Collins 1999).
Diet and Foraging: The rufous-crowned sparrow forages on the ground in herbage and in litter beneath shrubs, gleaning from ground and foliage; the species also gleans foliage of live oak, foraging predominantly on insects during the breeding season and including seeds, grasses, and forb shoots at other times of the year (Verner and Boss 1980; Bent 1968). Generally the diet is poorly known - it appears to vary with season, locality, and availability. It may eat more insects during the spring and summer and more seeds during the winter (Collins 1999).
Daily Activity: All Southern California rufous-crowned sparrow activities are focused on and around the ground, usually in the area of dense vegetative cover (Grinnell and Miller 1944; Bent 1968, Pulliam and Mills 1977; Root 1988). The species exhibits year-long, diurnal activity (Zeiner, et al. 1990). Males typically sing at all hours of the day with a peak activity in the early morning and late afternoon (Collins 1999).
Reproduction: The rufous-crowned sparrow breeds and feeds on steep, dry, herbage-covered hillsides with scattered shrubs and rock outcrops. Southern California rufous-crowned sparrows are relatively secretive, seeking cover in shrubs, rocks, grass and forb patches, concealing their nest on the ground at the base of a grass tussock or shrub or about 1 to 3 feet above the ground (Terres 1980; Verner and Boss 1980). The nest is cuplike and made of twigs, bark strips, grasses, and is lined with hair of deer, horses, and grasses (Terres 1980).
The rufous-crowned sparrow breeds from mid-March to mid-June with a peak in May. The egg dates for California are 11 March to 15 June with most occurring in April and May. The species is known to be monogamous; breeding territories may occur in groups (Pemberton 1910). The pairs are maintained throughout the year (Collins 1999). The clutch size is 2-5 eggs, and is usually 3 or 4 eggs. Incubation is by the female only, but the altricial young are tended by both parents (Harrison 1978). Incubation lasts about 11 to 13 days (Collins 1999). The nesting period is estimated to last 8 -9 days and at nest departure, the young are not completely feathered and their wings and tails are only partially grown. Fledglings are incapable of flight upon nest departure and are usually found either moving through low vegetation or hopping or running on the ground under protective cover of the vegetation (Collins 1999). Seasonal fecundity estimates for a population in southern California were 3.98 and 4.86 young/pair/season in 1996 and 1997 respectively (Collins 1999).
Survival: The oldest individual of the rufous-crowned sparrow that has been reported is 3 years, 2 months (Klimkiewicz and Futcher 1987).
Dispersal: The Southern California rufous-crowned sparrow is not migratory. There may be some movement up slope postbreeding to 1220 meters (4000 feet) in the western Sierra Nevada (Gaines 1977). It generally remains on or near the preferred breeding Habitat throughout the fall and winter. In the San Gabriel Mountains, individuals or pairs were observed during the fall in or near most of the territories used for breeding during the breeding season that had just finished. There may be limited postbreeding wandering of the young and adults into nearby Habitats that are not used for breeding (Collins 1999).
Socio-Spatial Behavior: Home range of the Southern California rufous-crowned sparrow, estimated from nesting density, was about 1.5 hectares (3.7 acres) in southern California chaparral (Cody 1974). In Arizona oak woodland, Balda (1969, 1970) reported six pairs and 11 pairs per 40 hectares (100 acres). In southern California coastal sage scrub, the territory size averages 2.0 acres with a range from 1.2 to 3.2 acres (Bent 1968). The species is not gregarious and is generally found in groups composed of no greater than five or six (Bent 1968) and apparently exist in scattered metapopulations across patchy landscapes. In southern California, territorial males are closely spaced in coastal sage scrub and more widely spaced in regrown (3-5 years post-fire) hard chaparral (Collins 1999).
Community Relationships: Eggs and nestlings of the Southern California rufous-crowned sparrow are preyed upon by snakes and small mammals (Bent 1968). Friedmann (1971) reported the first record of cowbird parasitism in this species. The Southern California rufous-crowned sparrow may occur in family groups postbreeding (Ehrlich, et al. 1988).
Threats to Species
The loss of coastal sage scrub for agriculture and urban development has reduced the available Habitat for the Southern California rufous-crowned sparrow (Bent 1968; Unitt 1984). Other stressors include a range of avian, mammalian and reptilian predators, both native and domestic, that find the ground-nesting habit of this bird as an easy target (Bent 1968). Long term fire suppression since the turn of the twentieth century may also have contributed to the reduction in numbers in California by allowing the chaparral and coastal sage scrub Habitats to grow into dense, decadent stands. It is only a rare host to brood parasitism of the brown-headed cowbird (Molothus ater) (Friedmann 1971, Collins 1999).
Special Biological Considerations
Although knowledge of Southern California rufous-crowned sparrows in the Plan Area appears to be limited, the species appears to have relatively broad Habitat preferences and a scattered distribution (Garrett and Dunn 1981).
Given the available information, this species apparently would benefit from steep slope preservation and maintenance of open edge conditions of coastal sage scrub that perpetuate herbaceous (grass and forb) elements. The limited use of prescribed fires may provide the disturbance that enhances foraging areas for this species.
Bolger et al. (1997) studied the 20-most common bird species within a 260 km2 area of coastal San Diego County in relation to edge/fragmentation sensitivity. Southern California rufous-crowned sparrow was found to be one of four species whose abundance is most reduced by presence of edges/fragmentation.
Declines in the populations in southern California suggest that the larger, interconnected blocks of open scrub Habitat suitable for maintaining this species over the long term should be preserved, particularly in areas under intense pressure from urban and irrigated or mechanized agricultural developments. Because this species can apparently tolerate a moderate amount of disturbance from prescribed burning and moderate levels of grazing, and because it usually inhabits moderate to steep slopes, management of its populations elsewhere in California and in other southwestern states may not be needed (Collins 1999). Moderate grazing and trampling by cattle on canyon slopes may benefit the rufous-crowned sparrow by opening up dense shrub Habitats (Collins 1999).
LITERATURE CITED
Balda, R. P. 1969. Foliage use by birds of the oak-juniper woodland and ponderosa pine forest in southeastern Arizona. Condor 71:399-412.
Balda, R. P. 1970. Effects of spring leaf-fall on composition and density of breeding birds in two southern Arizona woodlands. Condor 72:325-331.
Barlow, C. 1902. Some observations of the rufous-crowned sparrow. Condor 4:107-111.
Bent, A.C. 1968. Life histories of North American cardinals, grosbeaks, buntings, towhees, finches, sparrows, and allies. U.S. National Museum Bulletin 237:1889 pp.
Bolger, D. T., T. A. Scott and J. T. Rotenberry. 1997. Breeding bird abundance in an urbanizing landscape in coastal Southern California. Conservation Biology 11:406-421.
Cody, M. L. 1974. Competition and the structure of bird communities. Princeton Univ. Press, Princeton, NJ. 318pp.
Collins, P. W. 1999. Rufous-crowned Sparrow Aimophila ruficeps. No. 472. In The Birds of North America, A. Poole and F. Gill, Eds. Cornell Laboratory of Ornithology and the Academy of Natural Sciences.
Ehrlich, P.R., D.S. Dobkin, and O. Wheye. 1988. The Birder's Handbook: A Field Guide to the Natural History of North American Birds. New York, Simon and Schuster.
Friedmann, H. 1971. Further information on the host relations of the parasitic cowbirds. Auk 88:239-255.
Gaines, D. 1977. Birds of the Yosemite Sierra. California Syllabus, Oakland. 153 pp.
Garrett, K. and J. Dunn. 1981. Birds of Southern California: Status and Distribution. Los Angeles Audubon Society. 407 pp.
Grinnell, J. 1915. A distributional list of the birds of California. Pacific Coast Avifauna.
Grinnell, J. 1926. A new race of rufous-crowned sparrow from north-central Lower California. Auk: 43:244-245.
Grinnell, J. and A.H. Miller. 1944. The distribution of the birds of California. Pacific Coast Avifauna 27.
Harrison, C. 1978. A field guide to the nests, eggs and nestlings of North American birds. W. Collins Sons and Co., Cleveland, OH. 416pp.
Klimkiewicz, M. K., and A. G. Futcher. 1987. Longevity records of North American birds: Coerebinae through Estrilididae. J. Field Ornithology 58: 318-333.
Pemberton, J. R. 1910. Notes on the rufous-crowned sparrow. Condor 12:123-125.
Phillips, A., J. Marshall, and G. Monson. 1983. The birds of Arizona. University of Arizona Press, Tucson, AZ.
Pallium, H.R. and G. S. Mills. 1977. The use of space by wintering sparrows. Ecology 58:1391-1399.
Root, T.L. 1988. Atlas of wintering North American Birds: an analysis of Christmas Bird Count data. University of Chicago Press, Chicago, IL.
Terres, J. K. 1980. The Audubon Society Encyclopedia of North American Birds. Alfred A. Knopf, New York, New York. 1109pp.
Todd, W.E.C. 1922. A new sparrow from southern California. Condor 24:126-127.
Unitt, P. 1984. The Birds of San Diego County. San Diego Society of Natural History, San Diego, CA.
Verner, J., and A. B. Boss. 1980. California wildlife and their Habitats: western Sierra Nevada. U.S. Dept. Agriculture, Forest Service. Berkeley. General Technical Report PSW-37. 439 pp.
Willett, G. 1912. Birds of the Pacific slope of southern California. Pacific Coast Avifauna No.7.
Willett, G. 1933. A revised list of the birds of southwestern California. Pacific Coast Avifauna 21:1-204.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
southwestern willow flycatcher (Empidonax traillii extimus)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
southwestern willow flycatcher (Empidonax traillii extimus)
Status:
State: Endangered (all subspecies)
Federal: Endangered (Federal Register 60:10715, February 27, 1995); Partners in Flight Priority Bird Species; Cleveland National Forest Sensitive
GROUP DESIGNATION AND RATIONALE
Group 3
The southwestern willow flycatcher is narrowly distributed at few locations within the Plan Area. Although the preferred Habitat, riparian woodland and select other forests, is well distributed within all Bioregions and spread over the entire Plan Area, few current locations for the willow flycatcher have been documented. The southwestern willow flycatcher has specific Habitat requirements and conditions within the larger Habitat category within which it occurs. Because it requires specific Habitat conditions, occurs in few locations within a larger Habitat category, and occurs in low densities, the southwestern willow flycatcher will require conservation on a landscape level, site specific considerations for the known locations, and species specific management conditions as a Group 3 species.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 10,580 acres of suitable Habitat for the southwestern willow flycatcher including montane riparian forest, riparian scrub, arundo/riparian forest, riparian forest, southern cottonwood/willow riparian, southern sycamore/alder riparian woodland, and southern willow scrub.
Objective 2
Include within the MSHCP Conservation Area at least 6 Core Areas and interconnecting linkages. Core areas shall include the following areas: 1) Prado Basin/Santa Ana River, including Chino Creek, the Santa Ana River both up- and downstream of the Prado Dam, and the seven 2001 territories (9,670 acres); 2) Temescal Wash including Alberhill Creek (estimated as Subunit 3 plus Proposed Constrained Linkage 6 and Proposed Linkage 2; 4,290 acres); 3) Murrieta Creek (Proposed Constrained Linkage 13; 1,400 acres); 4) Temecula Creek (Proposed Constrained Linkages 14 and 24; 830 acres); 5) San Timoteo Canyon (Proposed Linkages 5, 12 and Proposed Linkage 22; 2,140 acres); 6) Vail Lake (Subunit 3 of Southwest Area Plan; 12,320 acres). Each Core Area will include at least 100 meters of undeveloped landscape adjacent to the riparian woodland and scrub Habitat and contain unfragmented Habitat and landscape linkages to other Core Areas.
Objective 3
Include within the MSHCP Conservation Area additional areas within the Criteria Area identified as important to the southwestern willow flycatcher. This Objective shall be met through implementation of the Protection of Species Associated with Riparian/Riverine Areas and Vernal Pools Policy presented in Section 6.1.2 of the MSHCP, Volume I. Wetland mapping assembled as part of that policy shall be reviewed as part of the project review process and if suitable southwestern willow flycatcher Habitat, defined as cottonwood or willow riparian Habitat adjacent to flowing water or saturated soils, is identified on the wetland maps and cannot be avoided, a focused survey for southwestern willow flycatcher shall be conducted by a qualified biologist in accordance with accepted protocol. If survey results are positive, 100 percent of the occupied portions of the property that provide for long-term conservation value for the flycatcher shall be conserved in a manner consistent with conservation of the flycatcher. This will involve including 100 meters of undeveloped landscape adjacent to the Habitat conserved. The survey requirements within this objective will be waived upon demonstrating that at least two Core Areas contain at least 10 successful flycatcher breeding pairs and at least four additional Core Areas each support breeding populations of at least 5 pairs of flycatchers.
Objective 4
Within the MSHCP Conservation Area, maintain (once every 3 years) the continued use of, and successful reproduction at 75 percent of the known southwestern willow flycatcher occupied Core Areas (including any nesting locations identified in the MSHCP Conservation Area in the future). Successful reproduction is defined as a nest which fledged at least one known young.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
For the purpose of the conservation analysis, potential Habitat for the southwestern willow flycatcher includes cottonwood or willow riparian Habitat with or without a riparian scrub element within all Bioregions. The subcategories of riparian scrub, woodland, and forest that are included in the conservation analysis of the southwestern willow flycatcher include: montane riparian forest, riparian scrub, arundo/riparian forest, riparian forest, southern cottonwood/willow riparian, southern sycamore/alder riparian woodland, and southern willow scrub and exclude tamarisk scrub and mule fat scrub. The inclusion of areas not currently occupied within the MSHCP Conservation Area system provides the potential for the re-occupation of areas that were used historically. Arundo/ riparian forest subcategories of Habitat have been included because these areas provide Habitat improvement opportunities, are located within other areas of suitable Habitat, and include both the arundo and riparian forest categories which cannot be separated based on the mapping prepared for the Plan Area. Based on these Habitat considerations, the Plan Area supports approximately 13,800 acres of potential Habitat for the southwestern willow flycatcher. Table 1 shows the conservation and loss of potential Habitat for the southwestern willow flycatcher. Overall, approximately 10,580 acres (77 percent) of potential Habitat in the Plan Area will be conserved in Criteria Area and existing Public/Quasi-Public Lands.
This species occurs within the Forest Service lands as well as the lowland Bioregions as a breeding and foraging species. It occurs predominantly within riparian woodland and forest Habitats and includes approximately 1,330 acres of suitable riparian scrub and forest Habitats. Under the existing Forest Land allocation plan, these locations and Habitats generally are located within the San Mateo Canyon Wilderness Area, San Gorgonio Wilderness Area, and most of the roadless areas and include approximately 750 acres of suitable riparian scrub and forest Habitats within these designations. Some suitable Habitat also is present within the Verdugo, Garner and Rouse range allotments and include approximately 110 acres. No core population areas or current locations of the southwestern willow flycatcher have been identified within the Cleveland National Forest or San Bernardino National Forest within the Plan Area (Stephenson and Calcarone 1999). Conservation of riparian Habitats and removal of cattle grazing from areas potentially occupied by southwestern willow flycatcher within the forest service lands are important conservation methods for this species.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
SOUTHWESTERN WILLOW FLYCATCHER
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| All Bioregions | |||||||
| Riparian Scrub, Woodland, and Forest excluding tamarisk scrub and mule fat scrub | 13,800 | 3,390 | 7,190 | 10,580 | 360 | 2,860 | 3,220 |
| TOTAL | 13,800 | 3,390 (25%) |
7,190 (52%) |
10,580 (77%) |
360 (2%) |
2,860 (21%) |
3,220 (23%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
In addition, the Riparian/Riverine Areas and Vernal Pools policy described in Section 6.1.2, MSHCP Volume I, provides for conservation of wetlands which will protect some Habitat for this species through avoidance and minimization. Mitigation for impacts to wetlands shall be incorporated in accordance with the "No Net Loss" policy of federal and state wetland regulations. The proposed mitigation shall be directly related to the functions and values of the wetland as related to this species and result in equivalent replacement.
As described above, conservation of this species will be considered from a landscape perspective, especially in the more western lowlands along the Interstate 15/215 corridor. Providing additional suitable Habitat that is not currently occupied almost certainly will assist with the recovery of the species. In addition, 6 Core Areas that have been defined for the southwestern willow flycatcher as discussed below. There are also individual locations outside of these Core Areas that also will be addressed.
As described below in Data Characterization, 17 of the 34 relatively recent point localities have a high location precision. Of these 17 point localities, 4 (24 percent) will be inside the Criteria Area, 8 (47 percent) are located within Public/Quasi-Public Lands. Within the Criteria Area and Public/Quasi-Public designations, 10 of the 12 locations are within suitable Habitat as currently mapped. Of the 5 high precision points located outside the MSHCP Conservation Area, all are located outside suitable Habitat areas within existing residential/urban/ exotic areas, non-native grassland, or open water.
There are definable locations for focusing conservation efforts where the species is currently known to breed or has been documented to breed in the past. The Core Areas include the following areas: 1) Prado Basin/Santa Ana River, including Chino Creek, the Santa Ana River both up- and downstream of the Prado Dam, and the seven 2001 territories (9,670 acres); 2) Temescal Wash including Alberhill Creek (estimated as subunit 3 plus Proposed Constrained Linkage 6 and Proposed Linkage 2; 4,290 acres); 3) Murrieta Creek (Proposed Constrained Linkage 13; 1,400 acres); 4) Temecula Creek (Proposed Constrained Linkages 14 and 24; 830 acres); 5) San Timoteo Canyon (Proposed Linkages 5, 12 and Proposed Linkage 22; 2,140 acres); 6) Vail Lake (Subunit 3 of Southwest Area Plan; 12,320 acres). Each Core Area will include at least 100 meters of undeveloped landscape adjacent to the riparian woodland and scrub Habitat and contain unfragmented Habitat and landscape linkages to other Core Areas. A total of 30,650 acres of Core Areas are conserved by the MSHCP as Criteria Area or Public/Quasi-Public designations within large blocks of a variety of Habitats. Within the Core Area at the Prado Basin/Santa Ana River, there are 5,520 acres of suitable Habitat for the southwestern willow flycatcher with the MSHCP Conservation Area. In addition, there are several single locations that have been identified as recent occurrences of the southwestern willow flycatcher, although these locations have not been confirmed within the past year. These include Santa Rosa Plateau Nature Reserve, Box Springs Mountain, Lake Skinner, Potrero Creek, Bautista Creek, and at Canyon Lake. These locations are outside the Core Areas for the species but are preserved as Criteria Area or Public/Quasi-Public designations within large blocks of a variety of Habitats. Although the Canyon Lake area is not included within the Criteria Area or Public/Quasi-Public designation, the Proposed Linkage 7 provides protection for this location.
As a Group 3 species the conservation of the southwestern willow flycatcher requires species specific conservation measures. Objective 3 provides the conservation of additional areas within the Criteria Area that are identified as important to the southwestern willow flycatcher. Wetland mapping assembled as part of the Wetland Policy will be reviewed as part of the project review process and if suitable southwestern willow flycatcher Habitat, defined as cottonwood or willow riparian Habitat adjacent to flowing water or saturated soils, is identified on the wetland maps and cannot be avoided, a focused survey for southwestern willow flycatcher will be conducted by a qualified biologist in accordance with Wildlife Agencies accepted protocol. If survey results are positive, 100 percent of the occupied portions of the property that provide for long-term conservation value for the flycatcher will be conserved in a manner consistent with conservation of the flycatcher. This will involve including 100 meters of undeveloped landscape adjacent to the Habitat conserved. The survey requirements within this objective will be waived upon demonstrating that at least two Core Areas contain at least 10 successful flycatcher breeding pairs and at least four additional Core Areas each support breeding populations of at least 5 pairs of flycatchers. The MSHCP Plan also will maintain (once every 3 years) the continued use of, and successful reproduction at 75 percent of the known southwestern willow flycatcher occupied Core Areas (including any nesting locations identified in the MSHCP Conservation Area in the future). Successful reproduction is defined as a nest which fledged at least one known young.
MSHCP Conservation Area Configuration Issues
Several large blocks of Habitat supporting or potentially supporting the southwestern willow flycatcher will be conserved as Criteria Area and Public/Quasi-Public designations, including the Core Areas at the Prado Basin/Santa Ana River, including Chino Creek, the Santa Ana River both up- and downstream of the Prado Dam, and the seven 2001 territories, Temescal Wash including Alberhill Creek, Murrieta Creek, Temecula Creek, San Timoteo, and Vail Lake. Other large blocks of Habitat that may support the southwestern willow flycatcher or that may support drainages containing suitable riparian Habitat for the species include Santa Rosa Plateau Nature Reserve, Box Springs Mountain, Lake Skinner, Lake Mathews, Lake Perris area, Sycamore Canyon Regional Park, Potrero Creek, Wilson Creek, Bautista Creek, and lower San Jacinto River. Some of these large blocks of Habitat have not been mapped as recently containing southwestern willow flycatchers or large drainages with riparian Habitat. However, these Habitat blocks have smaller riparian systems that contain potentially suitable Habitat and could be occupied by southwestern willow flycatchers in the future. Accordingly, the small patches of riparian Habitat and the sites containing small numbers of flycatchers are likely to be just as important as the large population sites (Finch and Stoleson 2000). It has been hypothesized that this subspecies is comprised of a number of metapopulations and thus some of these smaller sites probably are a regional source of colonizers, at least in some years (Finch and Stoleson 2000). These small populations or single occurrences, documented above to be largely preserved are important to prevent further isolation of remaining breeding groups. Additionally, some of these smaller riparian Habitat patches may provide management and restoration opportunities that are no longer available within other occupied areas.
As such, the MSHCP Conservation Area will provide adequate Habitat linkages between Core Areas for this species and will include smaller drainages that may support small numbers of the species. The Prado Basin Core Area is linked along the Santa Ana River to San Bernardino and Orange counties. This riparian area is linked to the south by the Temescal Wash to Lake Mathews and Lake Elsinore. Riparian Habitat within the Vail Lake area is linked to the Lake Skinner-Diamond Valley Lake area via Tucalota Creek. The Vail Lake area is also linked to the Santa Rosa Plateau and then to the Santa Margarita River by the riparian Habitat in Temecula Creek and Murrieta Creek. The Badlands area provides a major Habitat block that provides a linkage to Potrero Creek and Lake Perris and San Jacinto Wildlife Area.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 10,580 acres of suitable Conserved Habitat and 6 Core Areas and the additional current known locations within large blocks of Habitat in the MSHCP Conservation Area. The MSHCP Conservation Area will maintain (once every 3 years) the continued use of, and successful reproduction at 75 percent of the known southwestern willow flycatcher occupied Core Areas (including any nesting locations identified in the MSHCP Conservation Area in the future). Implementation of Objective 3 will provide the conservation of additional areas within the Criteria Area that are identified as important to the southwestern willow flycatcher through wetland mapping assembled as part of the Protection of Species Associated with Riparian/Riverine Areas and Vernal Pools Policy (Section 6.1.2, Volume I). This objective provides for conservation of 100 percent of the occupied portions of the property that provide for long-term conservation value for the flycatcher. The survey requirements within this objective will be waived upon demonstrating that at least two Core Areas contain at least 10 successful flycatcher breeding pairs and at least four additional Core Areas each support breeding populations of at least 5 pairs of flycatchers. A complete summary of all MSHCP species survey requirements is provided in Appendix E, Volume I.
INCIDENTAL TAKE
About 3,220 acres (about 23 percent) of suitable southwestern willow flycatcher Habitat will be outside the Criteria Area and Public/Quasi-Public Lands and individuals within these areas may be subject to Incidental Take. However, implementation of the Protection of Species Associated with Riparian/Riverine Areas and Vernal Pools (Section 6.1.2, Volume I) and adjacency policies, avoidance of clearing of suitable Habitat in the breeding season and protection and management of 90 percent of the area with conservation value of any site where the species is found will minimize Take of the species. A total of 5 of 17 high precision points are located outside the MSHCP Conservation Area, all of which are located outside suitable Habitat areas within existing residential/ urban/exotic areas, non-native grassland, or open water. None of the Core Areas for the species and none of the current known locations are outside of the MSCHP Conservation Area.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The location database for the southwestern willow flycatcher contains a relatively large number of locations but only a few are current or accurate enough for describing the existing population within the Plan Area. Additionally, many older surveys reported observations of willow flycatchers but did not identify the subspecies. Because the other subspecies of the willow flycatcher migrate through the area, early season observations may be one of the other subspecies and the occurrence of the southwestern willow flycatcher may only be confirmed if it is documented to breed in the area or remains in the area for the duration of the breeding season. There are a total of 45 records within the University of California at Riverside (UCR) database for the southwestern willow flycatcher. Thirty-four of these records are relatively recent (dated from 1990 or later). A total of 17 of these recent records are of high mapping precision. The Habitat types of these recent and high precision records include riparian, residential, chaparral, alkali playa, grassland, or sage scrub. Survey results from the United States Fish and Wildlife Service (USFWS) surveys within Prado Basin (seven territories in 2001) may not be represented within the UCR database but are considered to be current and are considered to accurately reflect the population levels within the Prado Basin/Santa Ana River area (Pike et al. 2001). Location records associated with more upland Habitats or residential developments may reflect records that are no longer extant or, more likely, may be located within small pockets of riparian Habitat that are too small to map or are located adjacent to riparian Habitat.
A moderate to large amount of published literature is available on the southwestern willow flycatcher. Because it is a listed species and has been considered a sensitive species for a number of years, a number of studies have been conducted on its distribution and natural history. The literature available on this species includes natural history studies, nesting and physiological ecology studies, and information on the management of the species. There is minimal information available for the specific Plan Area.
Habitat and Habitat Associations
The southwestern willow flycatcher is restricted to riparian woodlands along streams and rivers with mature, dense stands of willows (Salix spp.), cottonwoods (Populus spp.) or smaller spring fed or boggy areas with willows or alders (Alnus spp.) (Sedgwick and Knopf 1992). It breeds in relatively dense riparian Habitats in all or parts of seven southwestern states from near sea level in California to over 2,600 meters (8,500 feet) in Arizona and Colorado (USFWS 2001). Riparian Habitat provides both breeding and foraging Habitat for the species. The southwestern willow flycatcher nests from zero to 13 feet above ground in thickets of trees and shrubs approximately 13 to 23 feet tall with a high percentage of canopy cover and dense foliage. The nest site plant community is typically even-aged, structurally homogeneous and dense (Brown 1988; Whitfield 1990; Sedgwick and Knopf 1992). Historically, the willow flycatcher nested primarily in willows and mule fat with a scattered overstory of cottonwood (Grinnell and Miller 1944). Following more recent changes in riparian plant communities in the region, the species still nests in willows where available but is also known to nest in thickets dominated by tamarisk and Russian olive (Hubbard 1987; Brown 1988). Typically, sites selected as song perches by male willow flycatchers show higher variability in shrub size than do nest sites and often include large central shrubs. Habitats not selected for either nesting or singing are riparian zones with greater distances between willow patches and individual willow plants (Sedgwick and Knopf 1992). Nesting willow flycatchers invariably prefer areas with surface water nearby (Phillips et al. 1966). Suitable southwestern willow flycatcher Habitat is less likely to occur in steep, confined streams as are found in narrow canyons (USFWS 2001). Suitable flycatcher Habitat is more likely to develop and develop in more extensive patches along lower gradient streams with wider floodplains, although there are exceptions to this (San Luis Rey River) (USFWS 2001).
The willow flycatcher exhibits vegetation preferences at three scales of vegetation measurement: microplot (central willow and four adjacent shrubs); mesoplot (0.07 hectare); and macroplot (flycatcher territory size) (Sedgwick and Knopf 1992). Nest sites were distinguished by high willow density and low variability in willow patch size and bush height. Song perch sites were characterized by large central shrubs, low central shrub vigor, and high variability in shrub size. Unused sites were characterized by greater distances between willows and willow patches, less willow coverage, and a smaller riparian zone width than either nest or song perch sites. Regardless of the plant species composition or height, occupied sites always have dense vegetation in the patch interior and in most cases this dense vegetation occurs within the first 3 to 4 meters above ground (USFWS 2001). In almost all cases, slow-moving or still surface water and or saturated soil will be present at or near the breeding sites during normal precipitation years (USFWS 2001).
Biogeography
The general breeding range of the southwestern willow flycatcher includes: southern California, Arizona, New Mexico, extreme southern portions of Nevada and Utah, far western Texas, southwestern Colorado, and extreme northwestern Mexico (USFWS 1993). The specific breeding range for this subspecies includes: Owens Valley, south fork of the Kern River, the Los Angeles Basin (Unitt 1987; Zeiner, et al. 1990), the Santa Ynez River near Buellton, the Prado Basin riparian forest in Riverside County, the Santa Margarita and San Luis Rey Rivers in San Diego County, Middle Peak in the Cuyamaca Mountains, and near Imperial Beach (Small 1974). Breeding populations also exist in southern Nevada, Arizona, and New Mexico (Garrett and Dunn 1981). Additionally, this taxon overwinters in Mexico (USFWS 1995). Important stopovers along the Rio Grande provide important refueling sites for flycatchers as they migrate between their breeding and wintering grounds (Yong and Finch 1997).
Males typically arrive in southern California at the end of April and females arrive approximately one week later and adults depart from the breeding territory in mid-August to early September (San Diego Natural History Museum 1995).
The migration routes and destination of the southwestern willow flycatcher are not well understood. The species has been reported to sing and defend winter territories in Mexico and Central America. The southwestern willow flycatcher most likely winters in Mexico, Central America, and perhaps northern South America, however, the Habitats it uses on the wintering grounds are unknown (USFWS 1993).
The four subspecies of the willow flycatcher are separated in the breeding ranges (five subspecies are described by one investigator ). The breeding ranges of E. t. traillii and E. t. campestris extend across the northern United States and southern Canada from New England and Nova Scotia west, through northern Wyoming and Montana and into British Columbia (USFWS 1995). These two subspecies have been treated as one by Unitt (1987). The subspecies adastus breeds from Colorado west of the plains, west through the Great Basin States and into the eastern portions of California, Oregon, and Washington. The breeding range of E. t. brewsteri extends from the central California coast north, through western Oregon and Washington to Vancouver Island (USFWS 1995). Finally, the subspecies E. t. extimus, of which this species account is the subject, is described in detail above. Observations of migrating flycatchers within the Plan Area may constitute the subspecies E. t. brewsteri. Breeding activity must be determined in order to confirm that the observation of a willow flycatcher is E. t. extimus (San Diego Natural History Museum 1995).
Based on survey data collected between 1993 and 1996, the total known population of southwestern willow flycatchers is estimated to be 549 territories. At least 386 of these territories have been documented as confirmed probably breeding pairs (Finch and Stoleson, 2000). Within California, it has been estimated there are 121 territories (Finch and Stoleson, 2000).
Known Populations Within Western Riverside County
The southwestern willow flycatcher is sparsely located from the Prado Basin and Santa Ana River southeast to the Vail Lake region. It has been recorded as a single location or very few locations currently or historically within Temescal Wash/Alberhill Creek, Canyon Lake, Temecula Creek, Box Springs Mountains, Bautista Creek, Vail Lake, Hemet Lake (old record), Santa Rosa Plateau Nature Reserve, Lake Mathews, Lake Skinner, Lake Perris, and Potrero Creek. The locations that have been recorded since 1990 within the Plan Area are: Prado Basin (3-5 territories; seven territories in 2001), Santa Ana River (3-5 territories), Box Springs Mountain, Alberhill Creek, Canyon Lake, Santa Rosa Plateau Nature Reserve, Temecula Creek (approximately 3 locations), Vail Lake (2-4 locations), Lake Skinner, Bautista Creek, and Potrero Creek (Hays 1998, pers. comm.). In 2001, a total of seven southwestern willow flycatcher home rages were detected in the Prado Basin two of which were documented to fledge young (Pike et al. 2001). The Core Areas for the southwestern willow flycatcher are considered to be the Prado Basin/Santa Ana River, Temescal Wash, Temecula Creek, Murrieta Creek, Vail Lake, and San Timoteo Creek. The willow flycatcher is documented to occur within the Santa Margarita River but outside the Plan Area (Zembal 1987). The population size in the Santa Margarita River from Camp Pendleton to Fallbrook, which is outside the western Riverside County area, is estimated at 16 to 25 territories (San Diego Natural History Museum 1995).
Biology
Genetics: The four willow flycatcher subspecies are distinguished primarily by subtle differences in color and morphology (Unitt 1987). The four subspecies of the willow flycatcher are segregated by their breeding ranges (five subspecies are described by one investigator) as described above. No other genetics studies have been reported.
Diet and Foraging: The southwestern willow flycatcher is an insectivore that forages within and above dense riparian vegetation, taking insects on the wing or gleaning them from foliage (USFWS 1993). This species also forages in areas adjacent to nest sites which may be more open (USFWS 1995). No information is available on specific prey species (USFWS 1993).
Daily Activity: The southwestern willow flycatcher is a diurnally active species that begins singing at a predawn hour while within the territory (San Diego Natural History Museum 1995).
Reproduction: Although nesting willow flycatchers of all subspecies prefer areas with surface water nearby (Harris, et al. 1986), the southwestern willow flycatchers in Prado Basin virtually always nest near surface water or saturated soil (The Nature Conservancy 1994). The female southwestern willow flycatcher performs nest construction lasting approximately three to eight days (San Diego Natural History Museum 1995). The southwestern willow flycatcher nests zero to 13 feet high in thickets of trees and shrubs approximately 13 to 23 feet tall with a high percentage of canopy cover and dense foliage. This species usually nests in the upright fork of a shrub but occasionally nests on horizontal limbs within trees and shrubs (Terres 1980). The nest site plant community is typically even-aged, structurally homogeneous and dense (Brown 1988, Whitfield 1990, Sedgwick and Knopf 1992). Historically, the southwestern willow flycatcher nested primarily in willows and mule fat with a scattered overstory of cottonwoods (Grinnell and Miller 1944). Following more recent changes in riparian plant communities in the region, the species still nests in willows where available, but is also known to nest in thickets dominated by tamarisk and Russian olive (Hubbard 1987; Brown 1988).
Southwestern willow flycatchers typically raise one brood per year (USFWS 1993). The clutch size ranges from two to five; the average clutch size is 3.4 eggs in coastal southern California. The species usually has a monogamous mating system within one nesting season although not all territorial males are mated (San Diego Natural History Museum 1995). The nest success of the southwestern willow flycatcher on the south Fork Kern River is calculated at 61 percent with 20 out of 29 active nests successful. Nest reuse is not common for most non-colonial, open-nesting passerines including the southwestern willow flycatcher. However, more recent studies have reported a low, but existing, percentage of nest reuse among this species (Yard and Brown 1999).
Survival: The nest success of the southwestern willow flycatcher on the south Fork Kern River is calculated at 61 percent with 20 out of 29 active nests successful. Predation rate at the same site is calculated to be 27.6 percent (Whitfield 1996).
Dispersal: The southwestern willow flycatcher fledgling leaves the nest at age 12-15 days in early July (USFWS 1993) and disperses from the natal territory at age 26-30 days minimum. About 25 percent of adults return to their territory from the previous year; at least 20 percent of juveniles return to the natal area which is usually two to four kilometers from the natal territory. Adults usually depart from their breeding territory between 12 August and 4 September (San Diego Natural History Museum 1995).
Socio-Spatial Behavior: The southwestern willow flycatcher has a home range that is larger than the defended territory. This species initiates territorial defense in late May. The territory size varies from 0.24 to 0.45 hectare. The species may pack a maximum number of territories in suitable Habitat. The documented maximum is six females and five males in 4.4 hectares (San Diego Natural History Museum 1995). Sogge, et al. (1997) as reported in USFWS (1995) found territorial flycatchers in Habitat patches ranging form 0.5 to 1.2 hectares (1.23 to 2.96 acres). Two Habitat patches of 0.5 and 0.9 hectare each supported two territories in this study (Sogge, et al. 1997). Southwestern willow flycatchers do not pack their territories into all available space within a Habitat (USFWS 2001). Instead, some territories are bordered by additional riparian Habitat that is not defended as a breeding territory, but may be important in attracting flycatchers to the site or in providing an environmental buffer and in providing post-nesting use and dispersal areas. Flycatchers often cluster their territories into small portions of riparian sites and major portions of the site may be occupied irregularly or not at all (USFWS 2001).
Community Relationships: Discriminant function analysis indicates that riparian birds exhibit significant differences in their use of nesting Habitat. Willow flycatchers and the yellow warbler consistently use the most similar Habitats (Brown and Trosset 1989).
Threats to Species
Once considered widespread and common breeders in southern California, including western Riverside County, the southwestern willow flycatcher has declined precipitously throughout its range during the last 50 years (Unitt 1987). Southwestern willow flycatcher occupied riparian Habitats tend to be widely separated by vast expanses of relatively arid and unsuitable lands (Unitt 1987).
The major threats to the species can be summarized as follows: the current or future destruction, modification, or curtailment of its Habitat and the nest parasitism by the brown-headed cowbird that affects its productivity (USFWS 1995):
Changes in riparian plant communities, as summarized in the following from USFWS (1995), have resulted in the reduction, degradation, and elimination of nesting Habitat for the southwestern willow flycatcher which has curtailed the range, distribution, and population size of this species. Loss and modification of southwestern riparian Habitats have occurred from urban and agricultural development, water diversion and impoundment, channelization, livestock grazing, off-road vehicle and other recreational uses, and hydrological changes resulting from these and other land uses. It is estimated that 91 percent of historic riparian Habitat has been lost in California due to widespread destruction. Overuse by livestock has been a major factor in the degradation and modification of riparian Habitats in the region. These effects include changes in the plant community structure and species composition and in the relative abundance of the species and plant density. Livestock grazing in riparian areas typically results in the reduction of plant species diversity and density (USFWS 1995).
Another likely factor in the loss and modification of the southwestern willow flycatcher Habitat is the invasion by the exotic tamarisk (Tamarix sp.) and giant reed (Arundo donax). This non-native species has spread rapidly along the watercourses in the southwestern region, typically at the expense of native riparian vegetation, especially cottonwood and willow plant communities (USFWS 1995).
Water developments and flood control projects also have likely reduced and modified the Habitat for the flycatcher. The series of dams along most major southwestern rivers have altered riparian Habitats downstream of the dams through hydrological changes, vegetational changes, and inundated Habitats upstream. New Habitat may be created along the shoreline of the reservoirs but this Habitat is often unstable because of fluctuating levels of regulated reservoirs. Diversion and channelization of natural watercourses results in diminished surface flows and increased salinity of residual flows. Consequent reductions and composition changes in riparian vegetation are likely. Channelization often alters streambanks and fluvial dynamics necessary to maintain the native riparian vegetation. Logging in the upper watersheds of some of the southwestern rivers may constitute another potential threat to the southwestern willow flycatcher. This activity increases the likelihood of damaging floods in the Habitat (USFWS 1995).
Brood parasitism by the brown-headed cowbird also threatens the southwestern willow flycatcher (USFWS 1995). Cowbirds lay their eggs in the nests of other songbirds. The cowbird often removes a number of the host's eggs and replaces them with an equal number of cowbird eggs. Cowbird eggs require a relatively short incubation period; thus, the young cowbird hatches earlier than the remaining host's eggs. The effects of parasitism include reducing nest success rate and egg-to-fledging rate and delaying successful fledging. A common response to parasitism is abandonment of the nest. The success rate of renesting is often reduced and there may be inadequate time to prepare for migration. In California, parasitism rates range from 50 percent to 80 percent, which is considered to be a high parasitism rate (USFWS 1995, Verner and Ritter 1983).
Special Biological Considerations
The southwestern willow flycatcher prefers healthy riparian forests with structural diversity which provide nest cover and diverse insect populations (USFWS 1995). This subspecies is often present and singing on territories from late-April until late-August in southern California (USFWS 1995). It nests in thickets of trees and shrubs with dense foliage and appears to require dense vegetation (USFWS 1995). Although nesting willow flycatchers of all subspecies prefer areas with surface water nearby (Harris et al. 1986), the southwestern willow flycatchers in Prado Basin virtually always nest near surface water or saturated soil (The Nature Conservancy 1994).
Flood control projects generally shorten, straighten, and narrow river channels with the aim of producing unobstructed pathways to convey floodwaters. These projects can severely reduce the extent of alluvial influenced floodplain by cutting off main channels from side channels and adjacent floodplains and by reducing the meander patterns which slows stream velocity and dampen the effects of flooding. Channelization alters streambanks, typically elevating them well above the groundwater levels and thus preventing the roots of most native riparian shrubs and trees from accessing the groundwater. Overbank flooding necessary to deposit sediments, disperse seeds, rehydrate floodplain soils, and flush accumulations of salts, is reduced or precluded. Channel cutting further reduces water tables adjacent to the river, precluding seedling establishment because of the increased depth to groundwater. Channelization can increase the intensity of extreme floods, because reductions in upstream storage capacity produce accelerated water flow downstream. Channelization also reduces the width of wooded riparian Habitats, increasing the proportion of edge (Finch and Stoleson 2000).
Overuse by livestock has been a major factor in the degradation and modification of riparian Habitats in the region (USFWS 1995). In a study in Oregon on the effects of cattle grazing on riparian Habitat, a negative correlation was found between shrub volume and the frequency of cattle use (Taylor and Littlefield 1986). A positive correlation was found between the time since a transect was last grazed by cattle and shrub volume. Photographic evidence substantiated the improvement in riparian vegetation when protected from cattle in this study. Willow flycatchers were found in high numbers only on transects with high shrub volume and which were either undisturbed or rarely used by cattle. They were in low numbers or absent on transects with heavy cattle use and low shrub volume. The willow flycatcher population increases coincide with a dramatic decrease in cattle on the refuge and the elimination of willow cutting and spraying. The transect data show that the high numbers of the species are correlated with the amounts of healthy willows which are used for nesting sites. Willow flycatchers nest within two meters of the ground. Their nesting site is affected by the grazing because grazing causes notched or highlined willows that are top-heavy with high branches but with few live branches underneath (Taylor and Littlefield 1986).
Approximately one-half of the flycatcher nests in the Grand Canyon area show nest parasitism by the brown-headed cowbird (Sogge et al. 1997). This high rate of parasitism suggests that the bird is not effective in nest defense against cowbirds despite aggressive interactions between the species. The high parasitism rate is especially notable for a population that is generally small in size. Such a population is susceptible to blinking out under such high rates of parasitism or from other catastrophic events (Sogge et al. 1997). Cowbird control (trapping, addling eggs, removing nestlings, and/or shooting) has been used as a management tool for several populations of the southwestern willow flycatcher, mostly in California (Harris 1991, Whitfield et al. 1999). In southern California, nesting success and young fledged/female increased from 23 percent and 1.04 young/female before cowbird trapping to 39 percent and 1.74 young/female after cowbird trapping. Unfortunately, there is little evidence of an increase in the number of flycatcher breeding pairs on the study site (Whitfield et al. 1999). Other factors (e.g., predation) are thought to limit the growth of this population. Cowbird management programs may be needed to increase flycatcher reproductive success over the short term, but ultimately, the survival of the southwestern willow flycatcher will depend on the maintenance and restoration of riparian Habitats (Sedgwick 2000).
Vocalizations are a major component of the southwestern willow flycatcher breeding behavior, including the establishment of territories, courtship, and communication with conspecific and interspecific individuals (Krebs 1977). Recent studies of vocalization patterns in southwest willow flycatchers by Braden and McKernan (1998) indicate that vocalizations change during different stages of the nesting cycle. This is a critical factor to consider when attempting to identify this subspecies by vocalizations.
The willow flycatcher is more abundant in the continuous mesic shrub association than in other streamside vegetation structures including herbaceous xeric shrub or discontinuous mesic shrub (Sanders and Edge 1998). This species almost exclusively depends on hydrophytic shrub thickets for nesting in the semiarid western United States and is especially threatened by the elimination or simplification of continuous associations of mesic shrub vegetation. The investigators recommend that continuous associations of mesic shrub vegetation be maintained or restored where possible because this vegetation structure is associated with avian abundance, species richness, riparian-associated bird species abundance, and landscape-level biological diversity (Sanders and Edge 1998).
The differences between nest and song perch sites at the finer scales of vegetation description reflect their different functions. Therefore, the exclusive use of nest or song perch sites in vegetation analyses can result in misleading or at least incomplete descriptions of a species Habitat. Habitat interpretations for willow flycatchers are a function of the gender specific behavior of the birds observed and the scale of vegetation measurement (Sedgwick and Knopf 1992).
Nest reuse is not common for most non-colonial, open-nesting passerines including the southwestern willow flycatcher. However, more recent studies have reported a low, but existing, percentage of nest reuse among this species. Therefore, in order to properly monitor the southwestern willow flycatcher, investigators should consider reexamining previously used nests if a new nest cannot be found for a female which continues to exhibit nesting behavior (Yard and Brown 1999).
A potential course of Habitat management utilizes the relocation of beavers to more arid areas lacking riparian vegetation to restore this Habitat. It has been shown that this action has resulted in an increase in the southwestern willow flycatcher population. It is proposed that the beaver activity may slow the flow of water inducing sedimentation on the streambed thus raising the streambed elevation. This activity spreads water over a wider area enhancing pooling of water and restoration of the southwestern willow flycatcher's riparian Habitat (Albert 1999).
The high productivity and extent of riparian Habitat along the Santa Margarita River, Prado Basin, and the environs is reflected in the abundance and diversity of breeding birds. Within the growing population in southern California, the conversion of the remaining open spaces to other purposes will lead to continued pressure for additional encroachment on the floodplains. The desire for multiple use of these lands could perpetuate the trend of loss and degradation of riparian Habitat in the area. The importance of such Habitats strictly for wildlife use is essential to prevent the continued plan for multiple use of such Habitats. Currently, it should be emphasized in land planning scenarios, that the only acceptable uses of floodplains and associated riparian Habitat are the minimally destructive ones because the primary functions of such Habitats are best performed in a natural condition as possible (Zembal 1987).
The recovery plan for the southwestern willow flycatcher identifies a number of actions (USFWS 2001). These actions include increasing and improving breeding Habitat by restoring, mimicking, and/or recreating natural physical and biotic processes that influence riparian ecosystems, and reducing other stresses on the flycatcher. Specific actions include changing the management of surface and groundwater, including fundamental changes in dam operations, and restoring flood cycles, reducing impacts of domestic livestock, native ungulates, and feral horses and burros, improving metapopulation stability, securing long-term protection of breeding Habitat, managing exotic plant species, reducing brood parasitism by brown-headed cowbirds, and conducting research to refine management practices and knowledge of the ecology of the species (USFWS 2001).
LITERATURE CITED
Albert, S. 1999. The Beaver and the Flycatcher. Endangered Species Bulletin 24: 16-17.
Braden, G. T., and R. L. McKernan. 1998. Nest cycles, vocalizations, and survey protocols of the endangered southwestern willow flycatcher (Empidonax traillii extimus). Biological Sciences Section, San Bernardino County Museum. Report to U.S. Bureau of Reclamation, Lower Colorado River Office, Boulder City, Nevada. 36 pp.
Brown, B. T. 1988. Breeding ecology of a Willow Flycatcher population in Grand Canyon, Arizona. Western Birds 19: 25-33.
Brown, B. T., M. W. Trosset. 1989. Nesting-Habitat relationships of riparian birds along the Colorado River in Grand Canyon, Arizona (USA). Southwestern Naturalist 34:260-270.
Finch, D. M. and S. H. Stoleson, eds. 2000. Status, ecology, and conservation of the southwestern willow flycatcher. Gen. Tech. Rep. RMRS-GTR-60. Ogden, UT: U.S. Department of Agriculture, forest Service, Rocky Mountain Research Station. 131 pp.
Garrett, K., and J. Dunn. 1981. Birds of Southern California, status and distribution. Los Angeles Audubon Society. Los Angeles, California. 408pp.
Grinnell, J. and A. H. Miller. 1944. The Distribution of the birds of California. Pacific Coast Avifauna No. 27. Artemesia Press. Lee Vining, California. 615pp.
Harris, J. H. 1991. Effects of brood parasitism by brown-headed cowbirds on willow flycatcher nesting success along the Kern River, California. Western Birds 22: 13-26.
Harris, J. H., S. D. Sanders, and M. A. Flett. 1986. The status and distribution of the willow flycatcher in California, 1986. California Department of Fish and Game, Wildlife Management Division Administrative Report.
Hays, Loren. USFWS. 11/10/98. pers. comm.
Hubbard, J. P. 1987. The status of the Willow flycatcher in New Mexico. Endangered Species Program, New Mexico Dept. Of Game and Fish, Santa Fe, NM. 29 pp.
Krebs, J. R. 1977. The significance of song repertoires: the Beau Geste hypothesis. Animal Behavior 25:475-478.
Phillips, A. R., M. A. Howe, and W. E. Lanyon. 1966. Identification of the flycatchers of eastern North America, with special emphasis on the genus Empidonax. Bird-banding 37: 153-171.
Pike, J., D. Pellegrini, L. Hays, and R. Zembal. 2001. Least Bell's vireos and southwestern willow flycatchers in Prado Basin of the Santa Ana River watershed, CA. Prepared for Orange County Water District and the U.S. Fish and Wildlife Service.
Sanders, T. A. and W. D. Edge. 1998. Breeding bird community composition in relation to riparian vegetation structure in the western United States. Journal of Wildlife Management 62:461-473.
San Diego Natural History Museum. November 17, 1995. Empidonax extimus traillii in California: The Willow Flycatcher Workshop.
Sedgwick, J. A. 2000. Willow flycatcher Empidonax traillii. No. 533. In The Birds of North America. A. Poole and F. Gill, Eds. Cornell Laboratory of Ornithology, N.Y. and The Academy of Natural Sciences, Washington D. C.
Sedgwick, J. A., and F. L. Knopf. 1992. Describing willow flycatcher Habitats: scale perspectives and gender differences. Condor 94: 720-733.
Small, A. 1974. The Birds of California, Winchester Press, New York, NY.
Sogge, m. K., T. J. Tibbitts, and J. R. Petterson. 1997. Status and breeding ecology of the southwestern willow flycatcher in the Grand Canyon. Western Birds 28: 142-157.
Stephenson, J. R and G. M. Calcarone. 1999. Southern California mountains and foothills assessment: Habitat and species conservation issues. General Technical Report GTR-PSW-172. Albany, CA: Pacific Southwest Research Station, Forest Service, U.S. Department of Agriculture; 402 pp.
Taylor, D. M., and C. D. Littlefield. 1986. Willow flycatcher and yellow warbler response to cattle grazing. American Birds 40: 1169-1173.
Terres, J. K. 1980. The Audubon Society Encyclopedia of North American Birds. Alfred A. Knopf, New York, New York. 1109pp.
The Nature Conservancy. 1994. Status and distribution of the least Bell's vireo in the Prado Basin, California, 1986-1994. Unpublished draft report prepared for the Orange County Water District, County of Orange, California Department of Fish and Game, Corps of Engineers, and the U. S. Fish and Wildlife Service.
Unitt, P. 1987. Empidonax traillii extimus; An endangered subspecies. Western Birds 18:137-162.
U.S. Fish and Wildlife Service. 1993. Endangered and Threatened Wildlife and Plants; Proposed Rule to List the Southwestern Willow Flycatcher as Endangered with Critical Habitat. Federal Register 58:39495-39519.
U.S. Fish and Wildlife Service. 1995. Endangered and Threatened Wildlife and Plants; Final Rule Determining Endangered Status for the Southwestern Willow Flycatcher. Federal Register 60:10694-10715.
U.S. Fish and Wildlife Service. 1995. Internal Biological Opinion on the proposed issuance of recovery permits to Take the endangered southwestern willow flycatcher. 17 pp.
U.S. Fish and Wildlife Service. 2001. Draft Southwestern Willow Flycatcher Recovery Plan.
Albuquerque, New Mexico.
Verner, J. and L. V. Ritter. 1983. Current status of the brown-headed cowbird in the Sierra National Forest. Auk 100: 355-368.
Whitfield, M. J. 1990. Willow flycatcher reproductive response to Brown-headed Cowbird parasitism. Masters theses, Calif. State Univ., Chico. 25 pp.
Whitfield, M. J. 1996 Summary of Southwestern Willow Flycatchers on the South Fork Kern River, CA. Kern River Research Center.
Whitfield, M. J., K. M. Enos, and S. P. Rowe. 1999. Is brown-headed cowbird trapping effective for managing populations of the endangered southwestern willow flycatcher? Stud. Avian Biol. 18: 260-266.
Yong, W., and D. M. Finch. 1997. Migration of the willow flycatcher along the Middle Rio Grande. Wilson Bulletin 109:252-268.
Yard, Helen K. and Bryan T. Brown. 1999. Willow Flycatcher nest reuse in Arizona. Journal of Field Ornithology 70:720-733.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
Zembal, R. 1987. Riparian Habitat and breeding birds along the Santa Margarita and Santa Ana Rivers of southern California. In Conservation and Management of Rare and Endangered Plants. Thomas S. Elias, Ed. The California Native Plant society, Sacramento, California.
Swainson's hawk (Buteo swainsoni)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
southwestern willow flycatcher (Empidonax traillii extimus)
Status:
State: Endangered (all subspecies)
Federal: Endangered (Federal Register 60:10715, February 27, 1995); Partners in Flight Priority Bird Species; Cleveland National Forest Sensitive
GROUP DESIGNATION AND RATIONALE
Group 3
The southwestern willow flycatcher is narrowly distributed at few locations within the Plan Area. Although the preferred Habitat, riparian woodland and select other forests, is well distributed within all Bioregions and spread over the entire Plan Area, few current locations for the willow flycatcher have been documented. The southwestern willow flycatcher has specific Habitat requirements and conditions within the larger Habitat category within which it occurs. Because it requires specific Habitat conditions, occurs in few locations within a larger Habitat category, and occurs in low densities, the southwestern willow flycatcher will require conservation on a landscape level, site specific considerations for the known locations, and species specific management conditions as a Group 3 species.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 10,580 acres of suitable Habitat for the southwestern willow flycatcher including montane riparian forest, riparian scrub, arundo/riparian forest, riparian forest, southern cottonwood/willow riparian, southern sycamore/alder riparian woodland, and southern willow scrub.
Objective 2
Include within the MSHCP Conservation Area at least 6 Core Areas and interconnecting linkages. Core areas shall include the following areas: 1) Prado Basin/Santa Ana River, including Chino Creek, the Santa Ana River both up- and downstream of the Prado Dam, and the seven 2001 territories (9,670 acres); 2) Temescal Wash including Alberhill Creek (estimated as Subunit 3 plus Proposed Constrained Linkage 6 and Proposed Linkage 2; 4,290 acres); 3) Murrieta Creek (Proposed Constrained Linkage 13; 1,400 acres); 4) Temecula Creek (Proposed Constrained Linkages 14 and 24; 830 acres); 5) San Timoteo Canyon (Proposed Linkages 5, 12 and Proposed Linkage 22; 2,140 acres); 6) Vail Lake (Subunit 3 of Southwest Area Plan; 12,320 acres). Each Core Area will include at least 100 meters of undeveloped landscape adjacent to the riparian woodland and scrub Habitat and contain unfragmented Habitat and landscape linkages to other Core Areas.
Objective 3
Include within the MSHCP Conservation Area additional areas within the Criteria Area identified as important to the southwestern willow flycatcher. This Objective shall be met through implementation of the Protection of Species Associated with Riparian/Riverine Areas and Vernal Pools Policy presented in Section 6.1.2 of the MSHCP, Volume I. Wetland mapping assembled as part of that policy shall be reviewed as part of the project review process and if suitable southwestern willow flycatcher Habitat, defined as cottonwood or willow riparian Habitat adjacent to flowing water or saturated soils, is identified on the wetland maps and cannot be avoided, a focused survey for southwestern willow flycatcher shall be conducted by a qualified biologist in accordance with accepted protocol. If survey results are positive, 100 percent of the occupied portions of the property that provide for long-term conservation value for the flycatcher shall be conserved in a manner consistent with conservation of the flycatcher. This will involve including 100 meters of undeveloped landscape adjacent to the Habitat conserved. The survey requirements within this objective will be waived upon demonstrating that at least two Core Areas contain at least 10 successful flycatcher breeding pairs and at least four additional Core Areas each support breeding populations of at least 5 pairs of flycatchers.
Objective 4
Within the MSHCP Conservation Area, maintain (once every 3 years) the continued use of, and successful reproduction at 75 percent of the known southwestern willow flycatcher occupied Core Areas (including any nesting locations identified in the MSHCP Conservation Area in the future). Successful reproduction is defined as a nest which fledged at least one known young.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
For the purpose of the conservation analysis, potential Habitat for the southwestern willow flycatcher includes cottonwood or willow riparian Habitat with or without a riparian scrub element within all Bioregions. The subcategories of riparian scrub, woodland, and forest that are included in the conservation analysis of the southwestern willow flycatcher include: montane riparian forest, riparian scrub, arundo/riparian forest, riparian forest, southern cottonwood/willow riparian, southern sycamore/alder riparian woodland, and southern willow scrub and exclude tamarisk scrub and mule fat scrub. The inclusion of areas not currently occupied within the MSHCP Conservation Area system provides the potential for the re-occupation of areas that were used historically. Arundo/ riparian forest subcategories of Habitat have been included because these areas provide Habitat improvement opportunities, are located within other areas of suitable Habitat, and include both the arundo and riparian forest categories which cannot be separated based on the mapping prepared for the Plan Area. Based on these Habitat considerations, the Plan Area supports approximately 13,800 acres of potential Habitat for the southwestern willow flycatcher. Table 1 shows the conservation and loss of potential Habitat for the southwestern willow flycatcher. Overall, approximately 10,580 acres (77 percent) of potential Habitat in the Plan Area will be conserved in Criteria Area and existing Public/Quasi-Public Lands.
This species occurs within the Forest Service lands as well as the lowland Bioregions as a breeding and foraging species. It occurs predominantly within riparian woodland and forest Habitats and includes approximately 1,330 acres of suitable riparian scrub and forest Habitats. Under the existing Forest Land allocation plan, these locations and Habitats generally are located within the San Mateo Canyon Wilderness Area, San Gorgonio Wilderness Area, and most of the roadless areas and include approximately 750 acres of suitable riparian scrub and forest Habitats within these designations. Some suitable Habitat also is present within the Verdugo, Garner and Rouse range allotments and include approximately 110 acres. No core population areas or current locations of the southwestern willow flycatcher have been identified within the Cleveland National Forest or San Bernardino National Forest within the Plan Area (Stephenson and Calcarone 1999). Conservation of riparian Habitats and removal of cattle grazing from areas potentially occupied by southwestern willow flycatcher within the forest service lands are important conservation methods for this species.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
SOUTHWESTERN WILLOW FLYCATCHER
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| All Bioregions | |||||||
| Riparian Scrub, Woodland, and Forest excluding tamarisk scrub and mule fat scrub | 13,800 | 3,390 | 7,190 | 10,580 | 360 | 2,860 | 3,220 |
| TOTAL | 13,800 | 3,390 (25%) |
7,190 (52%) |
10,580 (77%) |
360 (2%) |
2,860 (21%) |
3,220 (23%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
In addition, the Riparian/Riverine Areas and Vernal Pools policy described in Section 6.1.2, MSHCP Volume I, provides for conservation of wetlands which will protect some Habitat for this species through avoidance and minimization. Mitigation for impacts to wetlands shall be incorporated in accordance with the "No Net Loss" policy of federal and state wetland regulations. The proposed mitigation shall be directly related to the functions and values of the wetland as related to this species and result in equivalent replacement.
As described above, conservation of this species will be considered from a landscape perspective, especially in the more western lowlands along the Interstate 15/215 corridor. Providing additional suitable Habitat that is not currently occupied almost certainly will assist with the recovery of the species. In addition, 6 Core Areas that have been defined for the southwestern willow flycatcher as discussed below. There are also individual locations outside of these Core Areas that also will be addressed.
As described below in Data Characterization, 17 of the 34 relatively recent point localities have a high location precision. Of these 17 point localities, 4 (24 percent) will be inside the Criteria Area, 8 (47 percent) are located within Public/Quasi-Public Lands. Within the Criteria Area and Public/Quasi-Public designations, 10 of the 12 locations are within suitable Habitat as currently mapped. Of the 5 high precision points located outside the MSHCP Conservation Area, all are located outside suitable Habitat areas within existing residential/urban/ exotic areas, non-native grassland, or open water.
There are definable locations for focusing conservation efforts where the species is currently known to breed or has been documented to breed in the past. The Core Areas include the following areas: 1) Prado Basin/Santa Ana River, including Chino Creek, the Santa Ana River both up- and downstream of the Prado Dam, and the seven 2001 territories (9,670 acres); 2) Temescal Wash including Alberhill Creek (estimated as subunit 3 plus Proposed Constrained Linkage 6 and Proposed Linkage 2; 4,290 acres); 3) Murrieta Creek (Proposed Constrained Linkage 13; 1,400 acres); 4) Temecula Creek (Proposed Constrained Linkages 14 and 24; 830 acres); 5) San Timoteo Canyon (Proposed Linkages 5, 12 and Proposed Linkage 22; 2,140 acres); 6) Vail Lake (Subunit 3 of Southwest Area Plan; 12,320 acres). Each Core Area will include at least 100 meters of undeveloped landscape adjacent to the riparian woodland and scrub Habitat and contain unfragmented Habitat and landscape linkages to other Core Areas. A total of 30,650 acres of Core Areas are conserved by the MSHCP as Criteria Area or Public/Quasi-Public designations within large blocks of a variety of Habitats. Within the Core Area at the Prado Basin/Santa Ana River, there are 5,520 acres of suitable Habitat for the southwestern willow flycatcher with the MSHCP Conservation Area. In addition, there are several single locations that have been identified as recent occurrences of the southwestern willow flycatcher, although these locations have not been confirmed within the past year. These include Santa Rosa Plateau Nature Reserve, Box Springs Mountain, Lake Skinner, Potrero Creek, Bautista Creek, and at Canyon Lake. These locations are outside the Core Areas for the species but are preserved as Criteria Area or Public/Quasi-Public designations within large blocks of a variety of Habitats. Although the Canyon Lake area is not included within the Criteria Area or Public/Quasi-Public designation, the Proposed Linkage 7 provides protection for this location.
As a Group 3 species the conservation of the southwestern willow flycatcher requires species specific conservation measures. Objective 3 provides the conservation of additional areas within the Criteria Area that are identified as important to the southwestern willow flycatcher. Wetland mapping assembled as part of the Wetland Policy will be reviewed as part of the project review process and if suitable southwestern willow flycatcher Habitat, defined as cottonwood or willow riparian Habitat adjacent to flowing water or saturated soils, is identified on the wetland maps and cannot be avoided, a focused survey for southwestern willow flycatcher will be conducted by a qualified biologist in accordance with Wildlife Agencies accepted protocol. If survey results are positive, 100 percent of the occupied portions of the property that provide for long-term conservation value for the flycatcher will be conserved in a manner consistent with conservation of the flycatcher. This will involve including 100 meters of undeveloped landscape adjacent to the Habitat conserved. The survey requirements within this objective will be waived upon demonstrating that at least two Core Areas contain at least 10 successful flycatcher breeding pairs and at least four additional Core Areas each support breeding populations of at least 5 pairs of flycatchers. The MSHCP Plan also will maintain (once every 3 years) the continued use of, and successful reproduction at 75 percent of the known southwestern willow flycatcher occupied Core Areas (including any nesting locations identified in the MSHCP Conservation Area in the future). Successful reproduction is defined as a nest which fledged at least one known young.
MSHCP Conservation Area Configuration Issues
Several large blocks of Habitat supporting or potentially supporting the southwestern willow flycatcher will be conserved as Criteria Area and Public/Quasi-Public designations, including the Core Areas at the Prado Basin/Santa Ana River, including Chino Creek, the Santa Ana River both up- and downstream of the Prado Dam, and the seven 2001 territories, Temescal Wash including Alberhill Creek, Murrieta Creek, Temecula Creek, San Timoteo, and Vail Lake. Other large blocks of Habitat that may support the southwestern willow flycatcher or that may support drainages containing suitable riparian Habitat for the species include Santa Rosa Plateau Nature Reserve, Box Springs Mountain, Lake Skinner, Lake Mathews, Lake Perris area, Sycamore Canyon Regional Park, Potrero Creek, Wilson Creek, Bautista Creek, and lower San Jacinto River. Some of these large blocks of Habitat have not been mapped as recently containing southwestern willow flycatchers or large drainages with riparian Habitat. However, these Habitat blocks have smaller riparian systems that contain potentially suitable Habitat and could be occupied by southwestern willow flycatchers in the future. Accordingly, the small patches of riparian Habitat and the sites containing small numbers of flycatchers are likely to be just as important as the large population sites (Finch and Stoleson 2000). It has been hypothesized that this subspecies is comprised of a number of metapopulations and thus some of these smaller sites probably are a regional source of colonizers, at least in some years (Finch and Stoleson 2000). These small populations or single occurrences, documented above to be largely preserved are important to prevent further isolation of remaining breeding groups. Additionally, some of these smaller riparian Habitat patches may provide management and restoration opportunities that are no longer available within other occupied areas.
As such, the MSHCP Conservation Area will provide adequate Habitat linkages between Core Areas for this species and will include smaller drainages that may support small numbers of the species. The Prado Basin Core Area is linked along the Santa Ana River to San Bernardino and Orange counties. This riparian area is linked to the south by the Temescal Wash to Lake Mathews and Lake Elsinore. Riparian Habitat within the Vail Lake area is linked to the Lake Skinner-Diamond Valley Lake area via Tucalota Creek. The Vail Lake area is also linked to the Santa Rosa Plateau and then to the Santa Margarita River by the riparian Habitat in Temecula Creek and Murrieta Creek. The Badlands area provides a major Habitat block that provides a linkage to Potrero Creek and Lake Perris and San Jacinto Wildlife Area.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 10,580 acres of suitable Conserved Habitat and 6 Core Areas and the additional current known locations within large blocks of Habitat in the MSHCP Conservation Area. The MSHCP Conservation Area will maintain (once every 3 years) the continued use of, and successful reproduction at 75 percent of the known southwestern willow flycatcher occupied Core Areas (including any nesting locations identified in the MSHCP Conservation Area in the future). Implementation of Objective 3 will provide the conservation of additional areas within the Criteria Area that are identified as important to the southwestern willow flycatcher through wetland mapping assembled as part of the Protection of Species Associated with Riparian/Riverine Areas and Vernal Pools Policy (Section 6.1.2, Volume I). This objective provides for conservation of 100 percent of the occupied portions of the property that provide for long-term conservation value for the flycatcher. The survey requirements within this objective will be waived upon demonstrating that at least two Core Areas contain at least 10 successful flycatcher breeding pairs and at least four additional Core Areas each support breeding populations of at least 5 pairs of flycatchers. A complete summary of all MSHCP species survey requirements is provided in Appendix E, Volume I.
INCIDENTAL TAKE
About 3,220 acres (about 23 percent) of suitable southwestern willow flycatcher Habitat will be outside the Criteria Area and Public/Quasi-Public Lands and individuals within these areas may be subject to Incidental Take. However, implementation of the Protection of Species Associated with Riparian/Riverine Areas and Vernal Pools (Section 6.1.2, Volume I) and adjacency policies, avoidance of clearing of suitable Habitat in the breeding season and protection and management of 90 percent of the area with conservation value of any site where the species is found will minimize Take of the species. A total of 5 of 17 high precision points are located outside the MSHCP Conservation Area, all of which are located outside suitable Habitat areas within existing residential/ urban/exotic areas, non-native grassland, or open water. None of the Core Areas for the species and none of the current known locations are outside of the MSCHP Conservation Area.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The location database for the southwestern willow flycatcher contains a relatively large number of locations but only a few are current or accurate enough for describing the existing population within the Plan Area. Additionally, many older surveys reported observations of willow flycatchers but did not identify the subspecies. Because the other subspecies of the willow flycatcher migrate through the area, early season observations may be one of the other subspecies and the occurrence of the southwestern willow flycatcher may only be confirmed if it is documented to breed in the area or remains in the area for the duration of the breeding season. There are a total of 45 records within the University of California at Riverside (UCR) database for the southwestern willow flycatcher. Thirty-four of these records are relatively recent (dated from 1990 or later). A total of 17 of these recent records are of high mapping precision. The Habitat types of these recent and high precision records include riparian, residential, chaparral, alkali playa, grassland, or sage scrub. Survey results from the United States Fish and Wildlife Service (USFWS) surveys within Prado Basin (seven territories in 2001) may not be represented within the UCR database but are considered to be current and are considered to accurately reflect the population levels within the Prado Basin/Santa Ana River area (Pike et al. 2001). Location records associated with more upland Habitats or residential developments may reflect records that are no longer extant or, more likely, may be located within small pockets of riparian Habitat that are too small to map or are located adjacent to riparian Habitat.
A moderate to large amount of published literature is available on the southwestern willow flycatcher. Because it is a listed species and has been considered a sensitive species for a number of years, a number of studies have been conducted on its distribution and natural history. The literature available on this species includes natural history studies, nesting and physiological ecology studies, and information on the management of the species. There is minimal information available for the specific Plan Area.
Habitat and Habitat Associations
The southwestern willow flycatcher is restricted to riparian woodlands along streams and rivers with mature, dense stands of willows (Salix spp.), cottonwoods (Populus spp.) or smaller spring fed or boggy areas with willows or alders (Alnus spp.) (Sedgwick and Knopf 1992). It breeds in relatively dense riparian Habitats in all or parts of seven southwestern states from near sea level in California to over 2,600 meters (8,500 feet) in Arizona and Colorado (USFWS 2001). Riparian Habitat provides both breeding and foraging Habitat for the species. The southwestern willow flycatcher nests from zero to 13 feet above ground in thickets of trees and shrubs approximately 13 to 23 feet tall with a high percentage of canopy cover and dense foliage. The nest site plant community is typically even-aged, structurally homogeneous and dense (Brown 1988; Whitfield 1990; Sedgwick and Knopf 1992). Historically, the willow flycatcher nested primarily in willows and mule fat with a scattered overstory of cottonwood (Grinnell and Miller 1944). Following more recent changes in riparian plant communities in the region, the species still nests in willows where available but is also known to nest in thickets dominated by tamarisk and Russian olive (Hubbard 1987; Brown 1988). Typically, sites selected as song perches by male willow flycatchers show higher variability in shrub size than do nest sites and often include large central shrubs. Habitats not selected for either nesting or singing are riparian zones with greater distances between willow patches and individual willow plants (Sedgwick and Knopf 1992). Nesting willow flycatchers invariably prefer areas with surface water nearby (Phillips et al. 1966). Suitable southwestern willow flycatcher Habitat is less likely to occur in steep, confined streams as are found in narrow canyons (USFWS 2001). Suitable flycatcher Habitat is more likely to develop and develop in more extensive patches along lower gradient streams with wider floodplains, although there are exceptions to this (San Luis Rey River) (USFWS 2001).
The willow flycatcher exhibits vegetation preferences at three scales of vegetation measurement: microplot (central willow and four adjacent shrubs); mesoplot (0.07 hectare); and macroplot (flycatcher territory size) (Sedgwick and Knopf 1992). Nest sites were distinguished by high willow density and low variability in willow patch size and bush height. Song perch sites were characterized by large central shrubs, low central shrub vigor, and high variability in shrub size. Unused sites were characterized by greater distances between willows and willow patches, less willow coverage, and a smaller riparian zone width than either nest or song perch sites. Regardless of the plant species composition or height, occupied sites always have dense vegetation in the patch interior and in most cases this dense vegetation occurs within the first 3 to 4 meters above ground (USFWS 2001). In almost all cases, slow-moving or still surface water and or saturated soil will be present at or near the breeding sites during normal precipitation years (USFWS 2001).
Biogeography
The general breeding range of the southwestern willow flycatcher includes: southern California, Arizona, New Mexico, extreme southern portions of Nevada and Utah, far western Texas, southwestern Colorado, and extreme northwestern Mexico (USFWS 1993). The specific breeding range for this subspecies includes: Owens Valley, south fork of the Kern River, the Los Angeles Basin (Unitt 1987; Zeiner, et al. 1990), the Santa Ynez River near Buellton, the Prado Basin riparian forest in Riverside County, the Santa Margarita and San Luis Rey Rivers in San Diego County, Middle Peak in the Cuyamaca Mountains, and near Imperial Beach (Small 1974). Breeding populations also exist in southern Nevada, Arizona, and New Mexico (Garrett and Dunn 1981). Additionally, this taxon overwinters in Mexico (USFWS 1995). Important stopovers along the Rio Grande provide important refueling sites for flycatchers as they migrate between their breeding and wintering grounds (Yong and Finch 1997).
Males typically arrive in southern California at the end of April and females arrive approximately one week later and adults depart from the breeding territory in mid-August to early September (San Diego Natural History Museum 1995).
The migration routes and destination of the southwestern willow flycatcher are not well understood. The species has been reported to sing and defend winter territories in Mexico and Central America. The southwestern willow flycatcher most likely winters in Mexico, Central America, and perhaps northern South America, however, the Habitats it uses on the wintering grounds are unknown (USFWS 1993).
The four subspecies of the willow flycatcher are separated in the breeding ranges (five subspecies are described by one investigator ). The breeding ranges of E. t. traillii and E. t. campestris extend across the northern United States and southern Canada from New England and Nova Scotia west, through northern Wyoming and Montana and into British Columbia (USFWS 1995). These two subspecies have been treated as one by Unitt (1987). The subspecies adastus breeds from Colorado west of the plains, west through the Great Basin States and into the eastern portions of California, Oregon, and Washington. The breeding range of E. t. brewsteri extends from the central California coast north, through western Oregon and Washington to Vancouver Island (USFWS 1995). Finally, the subspecies E. t. extimus, of which this species account is the subject, is described in detail above. Observations of migrating flycatchers within the Plan Area may constitute the subspecies E. t. brewsteri. Breeding activity must be determined in order to confirm that the observation of a willow flycatcher is E. t. extimus (San Diego Natural History Museum 1995).
Based on survey data collected between 1993 and 1996, the total known population of southwestern willow flycatchers is estimated to be 549 territories. At least 386 of these territories have been documented as confirmed probably breeding pairs (Finch and Stoleson, 2000). Within California, it has been estimated there are 121 territories (Finch and Stoleson, 2000).
Known Populations Within Western Riverside County
The southwestern willow flycatcher is sparsely located from the Prado Basin and Santa Ana River southeast to the Vail Lake region. It has been recorded as a single location or very few locations currently or historically within Temescal Wash/Alberhill Creek, Canyon Lake, Temecula Creek, Box Springs Mountains, Bautista Creek, Vail Lake, Hemet Lake (old record), Santa Rosa Plateau Nature Reserve, Lake Mathews, Lake Skinner, Lake Perris, and Potrero Creek. The locations that have been recorded since 1990 within the Plan Area are: Prado Basin (3-5 territories; seven territories in 2001), Santa Ana River (3-5 territories), Box Springs Mountain, Alberhill Creek, Canyon Lake, Santa Rosa Plateau Nature Reserve, Temecula Creek (approximately 3 locations), Vail Lake (2-4 locations), Lake Skinner, Bautista Creek, and Potrero Creek (Hays 1998, pers. comm.). In 2001, a total of seven southwestern willow flycatcher home rages were detected in the Prado Basin two of which were documented to fledge young (Pike et al. 2001). The Core Areas for the southwestern willow flycatcher are considered to be the Prado Basin/Santa Ana River, Temescal Wash, Temecula Creek, Murrieta Creek, Vail Lake, and San Timoteo Creek. The willow flycatcher is documented to occur within the Santa Margarita River but outside the Plan Area (Zembal 1987). The population size in the Santa Margarita River from Camp Pendleton to Fallbrook, which is outside the western Riverside County area, is estimated at 16 to 25 territories (San Diego Natural History Museum 1995).
Biology
Genetics: The four willow flycatcher subspecies are distinguished primarily by subtle differences in color and morphology (Unitt 1987). The four subspecies of the willow flycatcher are segregated by their breeding ranges (five subspecies are described by one investigator) as described above. No other genetics studies have been reported.
Diet and Foraging: The southwestern willow flycatcher is an insectivore that forages within and above dense riparian vegetation, taking insects on the wing or gleaning them from foliage (USFWS 1993). This species also forages in areas adjacent to nest sites which may be more open (USFWS 1995). No information is available on specific prey species (USFWS 1993).
Daily Activity: The southwestern willow flycatcher is a diurnally active species that begins singing at a predawn hour while within the territory (San Diego Natural History Museum 1995).
Reproduction: Although nesting willow flycatchers of all subspecies prefer areas with surface water nearby (Harris, et al. 1986), the southwestern willow flycatchers in Prado Basin virtually always nest near surface water or saturated soil (The Nature Conservancy 1994). The female southwestern willow flycatcher performs nest construction lasting approximately three to eight days (San Diego Natural History Museum 1995). The southwestern willow flycatcher nests zero to 13 feet high in thickets of trees and shrubs approximately 13 to 23 feet tall with a high percentage of canopy cover and dense foliage. This species usually nests in the upright fork of a shrub but occasionally nests on horizontal limbs within trees and shrubs (Terres 1980). The nest site plant community is typically even-aged, structurally homogeneous and dense (Brown 1988, Whitfield 1990, Sedgwick and Knopf 1992). Historically, the southwestern willow flycatcher nested primarily in willows and mule fat with a scattered overstory of cottonwoods (Grinnell and Miller 1944). Following more recent changes in riparian plant communities in the region, the species still nests in willows where available, but is also known to nest in thickets dominated by tamarisk and Russian olive (Hubbard 1987; Brown 1988).
Southwestern willow flycatchers typically raise one brood per year (USFWS 1993). The clutch size ranges from two to five; the average clutch size is 3.4 eggs in coastal southern California. The species usually has a monogamous mating system within one nesting season although not all territorial males are mated (San Diego Natural History Museum 1995). The nest success of the southwestern willow flycatcher on the south Fork Kern River is calculated at 61 percent with 20 out of 29 active nests successful. Nest reuse is not common for most non-colonial, open-nesting passerines including the southwestern willow flycatcher. However, more recent studies have reported a low, but existing, percentage of nest reuse among this species (Yard and Brown 1999).
Survival: The nest success of the southwestern willow flycatcher on the south Fork Kern River is calculated at 61 percent with 20 out of 29 active nests successful. Predation rate at the same site is calculated to be 27.6 percent (Whitfield 1996).
Dispersal: The southwestern willow flycatcher fledgling leaves the nest at age 12-15 days in early July (USFWS 1993) and disperses from the natal territory at age 26-30 days minimum. About 25 percent of adults return to their territory from the previous year; at least 20 percent of juveniles return to the natal area which is usually two to four kilometers from the natal territory. Adults usually depart from their breeding territory between 12 August and 4 September (San Diego Natural History Museum 1995).
Socio-Spatial Behavior: The southwestern willow flycatcher has a home range that is larger than the defended territory. This species initiates territorial defense in late May. The territory size varies from 0.24 to 0.45 hectare. The species may pack a maximum number of territories in suitable Habitat. The documented maximum is six females and five males in 4.4 hectares (San Diego Natural History Museum 1995). Sogge, et al. (1997) as reported in USFWS (1995) found territorial flycatchers in Habitat patches ranging form 0.5 to 1.2 hectares (1.23 to 2.96 acres). Two Habitat patches of 0.5 and 0.9 hectare each supported two territories in this study (Sogge, et al. 1997). Southwestern willow flycatchers do not pack their territories into all available space within a Habitat (USFWS 2001). Instead, some territories are bordered by additional riparian Habitat that is not defended as a breeding territory, but may be important in attracting flycatchers to the site or in providing an environmental buffer and in providing post-nesting use and dispersal areas. Flycatchers often cluster their territories into small portions of riparian sites and major portions of the site may be occupied irregularly or not at all (USFWS 2001).
Community Relationships: Discriminant function analysis indicates that riparian birds exhibit significant differences in their use of nesting Habitat. Willow flycatchers and the yellow warbler consistently use the most similar Habitats (Brown and Trosset 1989).
Threats to Species
Once considered widespread and common breeders in southern California, including western Riverside County, the southwestern willow flycatcher has declined precipitously throughout its range during the last 50 years (Unitt 1987). Southwestern willow flycatcher occupied riparian Habitats tend to be widely separated by vast expanses of relatively arid and unsuitable lands (Unitt 1987).
The major threats to the species can be summarized as follows: the current or future destruction, modification, or curtailment of its Habitat and the nest parasitism by the brown-headed cowbird that affects its productivity (USFWS 1995):
Changes in riparian plant communities, as summarized in the following from USFWS (1995), have resulted in the reduction, degradation, and elimination of nesting Habitat for the southwestern willow flycatcher which has curtailed the range, distribution, and population size of this species. Loss and modification of southwestern riparian Habitats have occurred from urban and agricultural development, water diversion and impoundment, channelization, livestock grazing, off-road vehicle and other recreational uses, and hydrological changes resulting from these and other land uses. It is estimated that 91 percent of historic riparian Habitat has been lost in California due to widespread destruction. Overuse by livestock has been a major factor in the degradation and modification of riparian Habitats in the region. These effects include changes in the plant community structure and species composition and in the relative abundance of the species and plant density. Livestock grazing in riparian areas typically results in the reduction of plant species diversity and density (USFWS 1995).
Another likely factor in the loss and modification of the southwestern willow flycatcher Habitat is the invasion by the exotic tamarisk (Tamarix sp.) and giant reed (Arundo donax). This non-native species has spread rapidly along the watercourses in the southwestern region, typically at the expense of native riparian vegetation, especially cottonwood and willow plant communities (USFWS 1995).
Water developments and flood control projects also have likely reduced and modified the Habitat for the flycatcher. The series of dams along most major southwestern rivers have altered riparian Habitats downstream of the dams through hydrological changes, vegetational changes, and inundated Habitats upstream. New Habitat may be created along the shoreline of the reservoirs but this Habitat is often unstable because of fluctuating levels of regulated reservoirs. Diversion and channelization of natural watercourses results in diminished surface flows and increased salinity of residual flows. Consequent reductions and composition changes in riparian vegetation are likely. Channelization often alters streambanks and fluvial dynamics necessary to maintain the native riparian vegetation. Logging in the upper watersheds of some of the southwestern rivers may constitute another potential threat to the southwestern willow flycatcher. This activity increases the likelihood of damaging floods in the Habitat (USFWS 1995).
Brood parasitism by the brown-headed cowbird also threatens the southwestern willow flycatcher (USFWS 1995). Cowbirds lay their eggs in the nests of other songbirds. The cowbird often removes a number of the host's eggs and replaces them with an equal number of cowbird eggs. Cowbird eggs require a relatively short incubation period; thus, the young cowbird hatches earlier than the remaining host's eggs. The effects of parasitism include reducing nest success rate and egg-to-fledging rate and delaying successful fledging. A common response to parasitism is abandonment of the nest. The success rate of renesting is often reduced and there may be inadequate time to prepare for migration. In California, parasitism rates range from 50 percent to 80 percent, which is considered to be a high parasitism rate (USFWS 1995, Verner and Ritter 1983).
Special Biological Considerations
The southwestern willow flycatcher prefers healthy riparian forests with structural diversity which provide nest cover and diverse insect populations (USFWS 1995). This subspecies is often present and singing on territories from late-April until late-August in southern California (USFWS 1995). It nests in thickets of trees and shrubs with dense foliage and appears to require dense vegetation (USFWS 1995). Although nesting willow flycatchers of all subspecies prefer areas with surface water nearby (Harris et al. 1986), the southwestern willow flycatchers in Prado Basin virtually always nest near surface water or saturated soil (The Nature Conservancy 1994).
Flood control projects generally shorten, straighten, and narrow river channels with the aim of producing unobstructed pathways to convey floodwaters. These projects can severely reduce the extent of alluvial influenced floodplain by cutting off main channels from side channels and adjacent floodplains and by reducing the meander patterns which slows stream velocity and dampen the effects of flooding. Channelization alters streambanks, typically elevating them well above the groundwater levels and thus preventing the roots of most native riparian shrubs and trees from accessing the groundwater. Overbank flooding necessary to deposit sediments, disperse seeds, rehydrate floodplain soils, and flush accumulations of salts, is reduced or precluded. Channel cutting further reduces water tables adjacent to the river, precluding seedling establishment because of the increased depth to groundwater. Channelization can increase the intensity of extreme floods, because reductions in upstream storage capacity produce accelerated water flow downstream. Channelization also reduces the width of wooded riparian Habitats, increasing the proportion of edge (Finch and Stoleson 2000).
Overuse by livestock has been a major factor in the degradation and modification of riparian Habitats in the region (USFWS 1995). In a study in Oregon on the effects of cattle grazing on riparian Habitat, a negative correlation was found between shrub volume and the frequency of cattle use (Taylor and Littlefield 1986). A positive correlation was found between the time since a transect was last grazed by cattle and shrub volume. Photographic evidence substantiated the improvement in riparian vegetation when protected from cattle in this study. Willow flycatchers were found in high numbers only on transects with high shrub volume and which were either undisturbed or rarely used by cattle. They were in low numbers or absent on transects with heavy cattle use and low shrub volume. The willow flycatcher population increases coincide with a dramatic decrease in cattle on the refuge and the elimination of willow cutting and spraying. The transect data show that the high numbers of the species are correlated with the amounts of healthy willows which are used for nesting sites. Willow flycatchers nest within two meters of the ground. Their nesting site is affected by the grazing because grazing causes notched or highlined willows that are top-heavy with high branches but with few live branches underneath (Taylor and Littlefield 1986).
Approximately one-half of the flycatcher nests in the Grand Canyon area show nest parasitism by the brown-headed cowbird (Sogge et al. 1997). This high rate of parasitism suggests that the bird is not effective in nest defense against cowbirds despite aggressive interactions between the species. The high parasitism rate is especially notable for a population that is generally small in size. Such a population is susceptible to blinking out under such high rates of parasitism or from other catastrophic events (Sogge et al. 1997). Cowbird control (trapping, addling eggs, removing nestlings, and/or shooting) has been used as a management tool for several populations of the southwestern willow flycatcher, mostly in California (Harris 1991, Whitfield et al. 1999). In southern California, nesting success and young fledged/female increased from 23 percent and 1.04 young/female before cowbird trapping to 39 percent and 1.74 young/female after cowbird trapping. Unfortunately, there is little evidence of an increase in the number of flycatcher breeding pairs on the study site (Whitfield et al. 1999). Other factors (e.g., predation) are thought to limit the growth of this population. Cowbird management programs may be needed to increase flycatcher reproductive success over the short term, but ultimately, the survival of the southwestern willow flycatcher will depend on the maintenance and restoration of riparian Habitats (Sedgwick 2000).
Vocalizations are a major component of the southwestern willow flycatcher breeding behavior, including the establishment of territories, courtship, and communication with conspecific and interspecific individuals (Krebs 1977). Recent studies of vocalization patterns in southwest willow flycatchers by Braden and McKernan (1998) indicate that vocalizations change during different stages of the nesting cycle. This is a critical factor to consider when attempting to identify this subspecies by vocalizations.
The willow flycatcher is more abundant in the continuous mesic shrub association than in other streamside vegetation structures including herbaceous xeric shrub or discontinuous mesic shrub (Sanders and Edge 1998). This species almost exclusively depends on hydrophytic shrub thickets for nesting in the semiarid western United States and is especially threatened by the elimination or simplification of continuous associations of mesic shrub vegetation. The investigators recommend that continuous associations of mesic shrub vegetation be maintained or restored where possible because this vegetation structure is associated with avian abundance, species richness, riparian-associated bird species abundance, and landscape-level biological diversity (Sanders and Edge 1998).
The differences between nest and song perch sites at the finer scales of vegetation description reflect their different functions. Therefore, the exclusive use of nest or song perch sites in vegetation analyses can result in misleading or at least incomplete descriptions of a species Habitat. Habitat interpretations for willow flycatchers are a function of the gender specific behavior of the birds observed and the scale of vegetation measurement (Sedgwick and Knopf 1992).
Nest reuse is not common for most non-colonial, open-nesting passerines including the southwestern willow flycatcher. However, more recent studies have reported a low, but existing, percentage of nest reuse among this species. Therefore, in order to properly monitor the southwestern willow flycatcher, investigators should consider reexamining previously used nests if a new nest cannot be found for a female which continues to exhibit nesting behavior (Yard and Brown 1999).
A potential course of Habitat management utilizes the relocation of beavers to more arid areas lacking riparian vegetation to restore this Habitat. It has been shown that this action has resulted in an increase in the southwestern willow flycatcher population. It is proposed that the beaver activity may slow the flow of water inducing sedimentation on the streambed thus raising the streambed elevation. This activity spreads water over a wider area enhancing pooling of water and restoration of the southwestern willow flycatcher's riparian Habitat (Albert 1999).
The high productivity and extent of riparian Habitat along the Santa Margarita River, Prado Basin, and the environs is reflected in the abundance and diversity of breeding birds. Within the growing population in southern California, the conversion of the remaining open spaces to other purposes will lead to continued pressure for additional encroachment on the floodplains. The desire for multiple use of these lands could perpetuate the trend of loss and degradation of riparian Habitat in the area. The importance of such Habitats strictly for wildlife use is essential to prevent the continued plan for multiple use of such Habitats. Currently, it should be emphasized in land planning scenarios, that the only acceptable uses of floodplains and associated riparian Habitat are the minimally destructive ones because the primary functions of such Habitats are best performed in a natural condition as possible (Zembal 1987).
The recovery plan for the southwestern willow flycatcher identifies a number of actions (USFWS 2001). These actions include increasing and improving breeding Habitat by restoring, mimicking, and/or recreating natural physical and biotic processes that influence riparian ecosystems, and reducing other stresses on the flycatcher. Specific actions include changing the management of surface and groundwater, including fundamental changes in dam operations, and restoring flood cycles, reducing impacts of domestic livestock, native ungulates, and feral horses and burros, improving metapopulation stability, securing long-term protection of breeding Habitat, managing exotic plant species, reducing brood parasitism by brown-headed cowbirds, and conducting research to refine management practices and knowledge of the ecology of the species (USFWS 2001).
LITERATURE CITED
Albert, S. 1999. The Beaver and the Flycatcher. Endangered Species Bulletin 24: 16-17.
Braden, G. T., and R. L. McKernan. 1998. Nest cycles, vocalizations, and survey protocols of the endangered southwestern willow flycatcher (Empidonax traillii extimus). Biological Sciences Section, San Bernardino County Museum. Report to U.S. Bureau of Reclamation, Lower Colorado River Office, Boulder City, Nevada. 36 pp.
Brown, B. T. 1988. Breeding ecology of a Willow Flycatcher population in Grand Canyon, Arizona. Western Birds 19: 25-33.
Brown, B. T., M. W. Trosset. 1989. Nesting-Habitat relationships of riparian birds along the Colorado River in Grand Canyon, Arizona (USA). Southwestern Naturalist 34:260-270.
Finch, D. M. and S. H. Stoleson, eds. 2000. Status, ecology, and conservation of the southwestern willow flycatcher. Gen. Tech. Rep. RMRS-GTR-60. Ogden, UT: U.S. Department of Agriculture, forest Service, Rocky Mountain Research Station. 131 pp.
Garrett, K., and J. Dunn. 1981. Birds of Southern California, status and distribution. Los Angeles Audubon Society. Los Angeles, California. 408pp.
Grinnell, J. and A. H. Miller. 1944. The Distribution of the birds of California. Pacific Coast Avifauna No. 27. Artemesia Press. Lee Vining, California. 615pp.
Harris, J. H. 1991. Effects of brood parasitism by brown-headed cowbirds on willow flycatcher nesting success along the Kern River, California. Western Birds 22: 13-26.
Harris, J. H., S. D. Sanders, and M. A. Flett. 1986. The status and distribution of the willow flycatcher in California, 1986. California Department of Fish and Game, Wildlife Management Division Administrative Report.
Hays, Loren. USFWS. 11/10/98. pers. comm.
Hubbard, J. P. 1987. The status of the Willow flycatcher in New Mexico. Endangered Species Program, New Mexico Dept. Of Game and Fish, Santa Fe, NM. 29 pp.
Krebs, J. R. 1977. The significance of song repertoires: the Beau Geste hypothesis. Animal Behavior 25:475-478.
Phillips, A. R., M. A. Howe, and W. E. Lanyon. 1966. Identification of the flycatchers of eastern North America, with special emphasis on the genus Empidonax. Bird-banding 37: 153-171.
Pike, J., D. Pellegrini, L. Hays, and R. Zembal. 2001. Least Bell's vireos and southwestern willow flycatchers in Prado Basin of the Santa Ana River watershed, CA. Prepared for Orange County Water District and the U.S. Fish and Wildlife Service.
Sanders, T. A. and W. D. Edge. 1998. Breeding bird community composition in relation to riparian vegetation structure in the western United States. Journal of Wildlife Management 62:461-473.
San Diego Natural History Museum. November 17, 1995. Empidonax extimus traillii in California: The Willow Flycatcher Workshop.
Sedgwick, J. A. 2000. Willow flycatcher Empidonax traillii. No. 533. In The Birds of North America. A. Poole and F. Gill, Eds. Cornell Laboratory of Ornithology, N.Y. and The Academy of Natural Sciences, Washington D. C.
Sedgwick, J. A., and F. L. Knopf. 1992. Describing willow flycatcher Habitats: scale perspectives and gender differences. Condor 94: 720-733.
Small, A. 1974. The Birds of California, Winchester Press, New York, NY.
Sogge, m. K., T. J. Tibbitts, and J. R. Petterson. 1997. Status and breeding ecology of the southwestern willow flycatcher in the Grand Canyon. Western Birds 28: 142-157.
Stephenson, J. R and G. M. Calcarone. 1999. Southern California mountains and foothills assessment: Habitat and species conservation issues. General Technical Report GTR-PSW-172. Albany, CA: Pacific Southwest Research Station, Forest Service, U.S. Department of Agriculture; 402 pp.
Taylor, D. M., and C. D. Littlefield. 1986. Willow flycatcher and yellow warbler response to cattle grazing. American Birds 40: 1169-1173.
Terres, J. K. 1980. The Audubon Society Encyclopedia of North American Birds. Alfred A. Knopf, New York, New York. 1109pp.
The Nature Conservancy. 1994. Status and distribution of the least Bell's vireo in the Prado Basin, California, 1986-1994. Unpublished draft report prepared for the Orange County Water District, County of Orange, California Department of Fish and Game, Corps of Engineers, and the U. S. Fish and Wildlife Service.
Unitt, P. 1987. Empidonax traillii extimus; An endangered subspecies. Western Birds 18:137-162.
U.S. Fish and Wildlife Service. 1993. Endangered and Threatened Wildlife and Plants; Proposed Rule to List the Southwestern Willow Flycatcher as Endangered with Critical Habitat. Federal Register 58:39495-39519.
U.S. Fish and Wildlife Service. 1995. Endangered and Threatened Wildlife and Plants; Final Rule Determining Endangered Status for the Southwestern Willow Flycatcher. Federal Register 60:10694-10715.
U.S. Fish and Wildlife Service. 1995. Internal Biological Opinion on the proposed issuance of recovery permits to Take the endangered southwestern willow flycatcher. 17 pp.
U.S. Fish and Wildlife Service. 2001. Draft Southwestern Willow Flycatcher Recovery Plan.
Albuquerque, New Mexico.
Verner, J. and L. V. Ritter. 1983. Current status of the brown-headed cowbird in the Sierra National Forest. Auk 100: 355-368.
Whitfield, M. J. 1990. Willow flycatcher reproductive response to Brown-headed Cowbird parasitism. Masters theses, Calif. State Univ., Chico. 25 pp.
Whitfield, M. J. 1996 Summary of Southwestern Willow Flycatchers on the South Fork Kern River, CA. Kern River Research Center.
Whitfield, M. J., K. M. Enos, and S. P. Rowe. 1999. Is brown-headed cowbird trapping effective for managing populations of the endangered southwestern willow flycatcher? Stud. Avian Biol. 18: 260-266.
Yong, W., and D. M. Finch. 1997. Migration of the willow flycatcher along the Middle Rio Grande. Wilson Bulletin 109:252-268.
Yard, Helen K. and Bryan T. Brown. 1999. Willow Flycatcher nest reuse in Arizona. Journal of Field Ornithology 70:720-733.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
Zembal, R. 1987. Riparian Habitat and breeding birds along the Santa Margarita and Santa Ana Rivers of southern California. In Conservation and Management of Rare and Endangered Plants. Thomas S. Elias, Ed. The California Native Plant society, Sacramento, California.
tree swallow (Tachycineta bicolor)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
tree swallow (Tachycineta bicolor)
Status:
State: None
Federal: Partners in Flight Priority Bird Species; San Bernardino National Forest Sensitive
GROUP DESIGNATION AND RATIONALE
Group 2
The tree swallow is widely but sparsely distributed throughout the MSHCP Plan Area within suitable Habitat. Breeding locations have been documented at Prado Basin and along the Santa Ana River. Additionally, Core Areas may be present at Wasson Canyon, Temecula Creek, Lake Skinner, Vail Lake, and Wilson Valley, based on repeated observations of tree swallows in these areas. The species has also been reported at Lake Mathews, Alberhill Creek, Lake Elsinore, Murrieta Creek, Lake Perris, and Santa Rosa Plateau. Because Habitat characteristics for this species are well known including open water for foraging and riparian scrub and water-associated woodland and forest for nesting, and the species occurs in all Bioregions of the Plan Area, but has specific locations that are Core Areas, it is anticipated that tree swallows will respond well to a landscape level with site specific requirements.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area 44,420 acres of suitable nesting and foraging Habitat for the tree swallow including open water, riparian scrub, woodland and forest, and oak woodland and forest Habitats in all Bioregions of the Plan Area.
Objective 2
Include within the MSHCP Conservation Area the 6 known Core Areas including the breeding populations in the Prado Basin/Santa Ana River (9,670 acres) and other Core Areas at Wasson Canyon (Subunit 5 of Elsinore Area Plan; 2,320 acres), Temecula Creek (Subunit 2 of Southwest Area Plan; 850 acres), Lake Skinner (Existing Core J plus Proposed Extension of Existing Cores 5, 6, 7; 29,060 acres), Vail Lake (Subunit 3 of Southwest Area Plan; 12,320 acres), and Wilson Valley (Subunit 2 of REMAP Area Plan; 33,540 acres). Include additional areas that may contain breeding populations including Lake Mathews, Lake Perris, and Lake Elsinore, and drainages and woodland areas within the Cleveland National Forest and San Bernardino National Forest.
Objective 3
Include within the MSHCP Conservation Area micro-Habitat (i.e., groups of large snags) in potential nesting Habitat.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
For the purpose of the conservation analysis, potential Habitat for the tree swallow includes riparian scrub, woodland, and forest Habitat, and oak woodland and forest Habitat which provides potential nest sites, and open water for foraging Habitat. Although the tree swallow nests within woodland areas that are near or adjacent to open water areas, these locations or acres cannot be quantified separately. The preferred Habitat for the tree swallow is encompassed within the Habitats included in this analysis. Additional protection of the microHabitat, which includes groups of snags, is included in the conservation analysis as Objective 3. Based on these Habitats, the Plan Area supports approximately 59,000 acres of potential Habitat for the tree swallow. Table 1 shows the conservation and loss of potential Habitat for the tree swallow. Overall, approximately 44,420 acres (75%) of potential Habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public Lands.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
TREE SWALLOW
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| All Bioregions | |||||||
| Riparian Scrub, Woodland, Forest | 14,610 | 3,920 | 7,270 | 11,190 | 370 | 3,050 | 3,420 |
| Oak Woodlands and Forest | 32,180 | 2,390 | 20,500 | 22,890 | 5,020 | 4,270 | 9,290 |
| Open Water | 12,210 | 1,190 | 9,150 | 10,340 | 40 | 1,830 | 1,870 |
| TOTAL | 59,000 | 7,500 (13%) |
36,920 (63%) |
44,420 (75%) |
5,430 (9%) |
9,150 (16%) |
14,580 (25%) |
1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area.
This species occurs within Forest Service lands as well as the lowland Bioregions as a breeding and wintering species. It occurs predominantly within riparian scrub, woodland and forest, and oak woodland and forest within the vicinity of water. Under the existing Forest Land allocation plan, these locations and Habitats generally are within the San Jacinto Wilderness Area, the San Mateo Canyon Wilderness Area, the roadless areas, and in most of the grazing allotments. Conservation of riparian and water-associated woodland Habitats within the Cleveland National Forest and San Bernardino National Forest will be important for conservation of this species.
The Riparian/Riverine Areas and Vernal Pools policy described in Section 6.1.2 of the MSHCP Volume I provides for conservation of wetlands which provide Habitat for this species through avoidance and minimization. Mitigation for impacts to wetlands shall be incorporated in accordance with the "No Net Loss" policy of federal and state wetland regulations. The proposed mitigation will be directly related to the functions and values of the wetland as related to this species and result in equivalent replacement.
As described below under Data Characterization, 9 of the relatively recent point localities have a high location precision. Of these 9 point localities, 3 (33 percent) will be inside the Criteria Area and 2 (22 percent) are located within Public/Quasi-Public Lands. Of the 4 high precision recent points located outside the MSHCP Conservation Area, none of the points are located within suitable breeding Habitat, they are all located within residential, non-native grassland, or sage scrub Habitats. These points are likely to be observations of the species in flight or foraging.
Conservation of this species will be considered from a landscape perspective because the suitable nesting and foraging Habitat has been well defined and conservation of additional suitable Habitat that may not currently be occupied may assist with the recovery of the species. In addition, there are definable locations composed of Core Areas and documented nesting areas for focusing conservation efforts including the nesting areas in Prado Basin/Santa Ana River (9,670 acres) and other Core Areas at Wasson Canyon (Subunit 5 of Elsinore Area Plan; 2,320 acres), Temecula Creek (Subunit 2 of Southwest Area Plan; 850 acres), Lake Skinner (Existing Core J plus Proposed Extension of Existing Cores 5, 6, 7; 29,060 acres), Vail Lake (Subunit 3 of Southwest Area Plan; 12,320 acres), and Wilson Valley (Subunit 2 of REMAP Area Plan; 33,540 acres). The total conservation of Core Areas includes 87,760 acres within large blocks of Habitat. Additional areas that may contain breeding populations including Lake Mathews, Lake Perris, and Lake Elsinore, and drainages and woodland areas within the Cleveland National Forest and San Bernardino National Forest will be conserved within Criteria Area and Public/Quasi-Public Lands. Within the potential nesting Habitat, the micro-Habitat, defined as groups of large snags, will be conserved within the MSHCP Conservation Area.
MSHCP Conservation Area Configuration Issues
Several large blocks of Habitat supporting or potentially supporting the tree swallow will be conserved as Criteria Area or Public/Quasi-Public designations, including the Prado Basin and along the Santa Ana River and other Core Areas at Wasson Canyon, Temecula Creek, Lake Skinner, Vail Lake and Wilson Valley. Other areas in which the species has been observed will be conserved including Lake Mathews, Lake Perris, Lake Elsinore, and Temescal Wash. The MSHCP Conservation Area will provide adequate Habitat linkages between Core Areas for this species and will include smaller drainages that may support small numbers of the species. The Prado Basin Core Area is linked along the Santa Ana River to San Bernardino and Orange counties. This riparian area is linked to the south by the Temescal Wash to Lake Mathews and Lake Elsinore. Riparian Habitat within the Vail Lake area is linked to the Lake Skinner-Diamond Valley Lake area via Tucalota Creek. The Vail Lake area is also linked to the Santa Rosa Plateau and then to the Santa Margarita River by the riparian Habitat in Temecula Creek and Murrieta Creek. The Badlands area provides a major Habitat block that provides a linkage to Potrero Creek, Lake Perris, and the San Jacinto Wildlife Area.
Conservation Summary
In summary, conservation for this species will be achieved by the inclusion of at least 44,420 acres of suitable Conserved Habitat in the MSHCP Conservation Area. In addition, implementation of Objective 3 for this species will conserve the micro-Habitat (i.e., groups of large snags) in potential nesting Habitat. The six Core Areas of the tree swallow are conserved within large blocks of Habitat in the MSHCP Conservation Area and additional areas where the tree swallow has been observed and that contain potential Habitat are also conserved.
INCIDENTAL TAKE
The Incidental Take of the tree swallow is difficult to quantify due to our limited knowledge of its distribution and abundance within the Plan Area. The maximum level of Incidental Take of tree swallows can be anticipated by the loss of the number of acres of potential Habitat that will become unsuitable for this species. About 14,580 acres (25 percent) of potential Habitat for the tree swallow will be outside the Criteria Area and Public/Quasi-Public Lands, and individuals within these areas will be subject to Incidental Take consistent with the Plan. None of the Core Areas will be outside the MSHCP Conservation Area. Of this, approximately 5,430 acres (9 percent) of potential Habitat are located within Rural/Mountainous designation areas. While the Rural/Mountainous areas are not included within the MSHCP Conservation Area, will not be managed for the benefit of wildlife, and the existing zoning/ordinances for these areas do not preclude development and could allow substantial fragmentation and/or degradation of Habitat for proposed covered species, the anticipated levels of development in these areas may be consistent with maintaining some Habitat for the tree swallow. It should also be noted that wetland Habitat Areas and Vernal Pools located outside the MSHCP Conservation Area would be subject to the Protection of Species Associated with Riparian/ Riverine Areas and Vernal Pools policy presented in Section 6.1.2 of the MSHCP, Volume I.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The UCR location database includes approximately 49 records for the tree swallow within the Plan Area dated from 1888 to 1999. Approximately 29 records are relatively recent (within the past 10 years) and of these recent records, nine are high precision records that can be accurately placed within the area. The Habitats types associated with these recent and high precision data records include riparian, sage scrub, orchard, grassland, and residential. The residential Habitat records may reflect records that are either no longer extant or where the location is a foraging observation of the species over a development area. Breeding locations of the species have not been recorded within the UCR database, however, they have been documented by the USFWS within the Prado Basin.
The literature available on the tree swallow is relatively low. It is focused on the natural history of the species, however, some of the details of its natural history have not been determined. A few general ornithological reference treatments have been prepared for the species. Little information is available with respect to the Plan Area other than general distribution and occurrence information.
Habitat and Habitat Associations
Although tree swallows may be found virtually anywhere in aerial Habitat during migration and winter (e.g., AOU 1998), birds forage primarily over and around ponds, marshes, rivers, lakes, and estuaries (Garrett and Dunn 1981). Tree swallows nest almost exclusively in cavity-containing trees or snags with cavities that are near, or preferably in, water (Grinnell and Miller 1944). Suitable Habitat is provided for the tree swallow by riparian forest and woodland up through the lodgepole pine belt for breeding Habitats. It frequents valley foothill and montane riparian Habitats below 2,700 meters (9,000 feet) for breeding within its range. In winter, it inhabits lowlands near estuaries, rivers, lakes, and emergent wetlands. In winter and migration, the species uses more open Habitats, grasslands, meadows, brushlands, and is also found near water sources but is not restricted to Habitat that contains cavities as is the case during the breeding season (Zeiner, et al. 1990).
Biogeography
Tree swallows breed locally from western Alaska eastward to Newfoundland southward to California and Georgia. The northern limit coincides approximately with the tree line. The species winters from Baja California along the Pacific coastline into Mexico, across Central America, along the Gulf of Mexico coast, throughout Florida and north along the Atlantic Coast to the Carolinas; it also winters southward to northern South America (AOU 1998).
Zeiner, et al. (1990) summarize the distribution, abundance, and seasonality of the tree swallow within California as follows. It is a common summer resident in central and northern California; uncommon south of San Francisco Bay. The species is a common to occasional transient throughout the state in virtually all non-desert Habitats. In winter, it is common in southern California at the Salton Sea and Colorado River, it is uncommon to rare in coastal California north to Sonoma County and in the Central Valley (Grinnell and Miller 1944, McCaskie, et al. 1979, 1988).
The first spring transients arrive in California in late January from Mexico and Central America. Numbers increase through the spring, but diminish in summer in southern California. In late summer and early fall, the numbers increase again as transients pass through from the north. Most of the migration has been completed by the end of October. Small numbers regularly winter on the coast north to central California, and in the Central Valley (Garrett and Dunn 1981).
The tree swallow winters primarily in Florida and along the Gulf of Mexico. It winters occasionally north to eastern Massachusetts and Long island, NY. Flocks of the tree swallow are encountered with regularity along the Caribbean coast of South America, east to northwestern Venezuela (Robertson et al. 1992).
The tree swallow was formerly a common breeder in lowland and foothill riparian Habitats within the coastal areas of southern California including the Plan Area. It is now a very local summer resident (Garrett and Dunn 1981).
The tree swallow has shown local but regular nesting since 1980 in central and western North Carolina and in Georgia, Arkansas, Alabama, Oklahoma and most of Tennessee, Kentucky and Missouri. This suggests a genuine southward expansion of the breeding range in the past decade (Robertson et al., 1992).
Known Populations Within Western Riverside County
The tree swallow is an uncommon to common migrant/transient and rare winter visitor in most of the coastal plain of southern California (including the Plan Area); the tree swallow is a rare and very local breeder in the Plan Area and southern California as a whole (Garrett and Dunn (1981). Its occurrence within the Plan Area as a winter visitant is rare and limited to areas around marshes and rivers (Garrett and Dunn 1981).
The only known breeding population within the Plan Area persists in the Prado Basin and adjacent Santa Ana River (Hays, 1999, pers. obs.; Patten, 1998, pers. comm.). The Prado Basin and Santa Ana River population consisted of approximately 20 pairs during the 1998 breeding season (Pike, 1998, pers. comm.). The tree swallow may have Core Areas within other areas that contain several observation records including Wasson Canyon, Temecula Creek, Lake Skinner, Vail Lake and Wilson Valley. Each of these locations has the required association with water over which they are frequently observed foraging and the required riparian and wooded Habitat that would provide opportunities for nesting. Although these locations have not been documented as breeding areas they could be used in the future or may not have had nesting areas documented or found. Due to the repeated observations, these areas are considered Core Areas in addition to the known breeding locations at Prado Basin and Santa Ana River.
Other locations that are recorded within the U.C. Riverside database include: Lake Elsinore, Temescal Wash, Murrieta Creek, San Jacinto Wildlife Area, Lake Perris, Lake Mathews, Santa Rosa Plateau West, and Motte-Rimrock Reserve. Although not documented to occur within the mountainous Bioregions, they are reported in the literature to occur in low numbers in higher elevation areas.
Biology
Genetics: At a higher taxonomic level, the closest relative of Tachycineta, which includes the tree swallow, appears to be either the bank swallows or a large and complex group of hole nesting species that radiated in the Andes (Sheldon and Winkler 1993). Knowledge of the inter-relationships of Tachycineta species remains poor and in need of further study.
Diet and Foraging: The tree swallows eat mostly flying insects in open areas above land or water from 0 to 50 meters (Robertson, et al. 1992). It feeds mostly on insects hawked in long, cruising flights. Individuals can subsist on seeds and berries for extended periods of time during harsh winters and these items may make up about 20 percent of the diet (Bent 1942; Robertson, et al. 1992).
Daily Activity: During the breeding season, male and female tree swallows protect the nest 50 to 60 percent of the day (Robertson, et al. 1992). The tree swallow forages from dawn to dusk. During the early part of the breeding season, the species feeds most actively during the late morning and afternoon and frequently departs from the nesting site around midday (Robertson et al. 1992).
Reproduction: Nesting of the tree swallow occurs almost exclusively in cavity-containing trees that are near, or preferably in, water (Grinnell and Miller 1944). It chiefly nests in an old woodpecker hole, but also on cliff or bank, in nest box, or other human-made structure. Nesting trees are often in beaver ponds and wetland margins providing open areas near water (Robertson, et al. 1992). Natural cavities typically occur in standing dead trees from about one to ten meters above the substrate. Entrance holes are typically four to nine centimeters in diameter, with cavities 10 to 20 centimeters deep. The tree swallow may also nest in short, hollow stumps over water and sometimes nest in unusual locations such as eaves of buildings, wood duck nest boxes, steel drums and old cliff swallow nests. The nest is made mostly of twigs and other plant materials and lined with feathers.
Tree swallows are monogamous, but exhibit extra-pair copulations frequently (Robertson, et al. 1992). One study found 50 percent of nests contained offspring not descendent of the occupied male (Robertson, et al. 1992). It breeds in mid-April to mid-August with a peak in activity in May and June. It usually nests solitarily, but sometimes in small groups, depending on nest site availability (Bent 1942). The clutch size for this species ranges from two to eight eggs and is most commonly four to seven (Robertson, et al. 1992; Moller 1991). The species is often double-brooded. Incubation lasts for 13-16 days. The altricial young are tended by both adults, and fledge at 16-24 days (Harrison 1978). Yearlings of the tree swallow are able to breed (Robertson, et al. 1992).
Survival: Nesting success of the tree swallow has been measured at 78.8 percent; this measure has been observed to be drastically reduced under poor weather conditions (Robertson, et al. 1992). Maximum life span recorded was between eight and eleven years (Robertson, et al. 1992). Mortality during the first year takes 79 percent of one-year birds with a 40 to 60 percent annual survival rate thereafter (Robertson, et al. 1992).
Dispersal: The tree swallow is a north-south continent migrant (Robertson, et al. 1992). Nestlings typically are active within three days and leave the nest after 18 to 22 days (Robertson, et al. 1992). The proportion of the banded nestlings that return to an area the next year ranges from 0.8 to 12 percent (Butler 1988). The proportion of breeding adults that return to the same area to breed the next year ranges from 13 to 60 percent. Variation in winter mortality affects the return rates as does the average breeding success of the population from the previous year (Butler 1988).
Socio-Spatial Behavior: Tree swallows often form large flocks of several hundred thousand birds outside of the breeding season (Robertson, et al. 1992). At one perch site, individuals were observed to be spaced approximately 10 cm apart (Robertson, et al. 1992). Kuerzi (1941) stated the home range for the species is "large." Home range varies in different areas but probably extends 60 kilometers or more prior to incubation (Robertson, et al. 1992).
Both sexes of the tree swallow are both inter- and intra-specifically territorial in defending their nests. The actual defended territory is restricted to the nest site (Kuerzi 1941). Nests are typically spaced 10 to 15 meters apart and birds are solitary at this time (Robertson, et al. 1992). In the Sierra Nevada, densities of nesting pairs per 40 hectares (100 acres) included 4-18 in riparian Habitat and 2-10 in mixed conifer forest (Raphael and White 1978). Pairs often defend nests and extra nest-sites up to a 56 meter area (Rendell and Robertson 1994). Individuals will tend to space their nests as far as possible, as demonstrated in an artificial study (Muldal, et al. 1985).
Community Relationships: Competition for suitable tree swallow nesting Habitat occurs with both primary and secondary cavity nesters and includes house wrens, house sparrows, northern flickers and others (Robertson, et al. 1992). Predators of eggs and nestlings include snakes, raccoons, bears, large birds, deer mice and feral cats (Robertson, et al. 1992). In one study, clutch mortality was found to be higher in an area where nest interference by house wrens occurs (Finch 1990). As with other swallows, the adults are swift fliers and infrequently fall prey to hawks.
Threats to Species
Garrett and Dunn (1981) concluded that the decline of the tree swallow species as a breeder in southern California was likely a result of the destruction of riparian groves, removal of snags, and competition with the introduced European starling (Sturnus vulgaris) for nesting cavities. European starlings only rarely have been recorded within the Prado Basin, which is the only known tree swallow nesting area in the Plan Area. Tree swallows were formerly common breeders in lowland and foothill riparian areas in southern California from San Luis Obispo County to San Diego County (Garrett and Dunn 1981). Habitat destruction and water pollution in the breeding and wintering areas may affect tree swallows. The loss of marshes and other wetlands can result in greater concentrations of birds into smaller areas for roosting and breeding and consequently may result in local depletion of food supplies or vulnerability to adverse local conditions (Robertson et al. 1992).
PCBs and high levels of DDE have been found in adults, eggs and nestlings and may harm the species although eggshell thinning has not been documented (Robertson, et al. 1992). Acid rain has been shown to reduce reproductive success. In clear-cut regrowth forests, nest predation varied with patch age, being highest in the youngest patches (Blancher and McNicol 1991). Reproductive success was also lower in individuals breeding below electrical power lines (Doherty and Grubb 1998).
Special Biological Considerations
Tree swallows respond to the forest edge by avoiding nesting near the edge (Holt and Martin 1997; Rennell and Robertson 1990). Forest management in which dead snags are left standing is extremely important to tree swallows as well as to other birds that need existing cavities for nesting. In Washington, both density and species diversity of cavity nesters, including tree swallows, are greater on plots where snags have not been removed (Zarnowitz and Manuwal 1985).
Breeding populations of tree swallows are limited by the availability of nest sites which in turn likely limits the population size (Robertson, et al. 1992). Individuals will use nest boxes, have been shown to preferentially select them, and clutch size is higher in nest boxes (Robertson and Rendell 1990). Because tree swallows apparently are amenable locally to using nest boxes (Purvis, 1998, pers. comm., 1998), management of the species in some areas may be relatively successful in establishing breeding colonies and increasing breeding productivity.
LITERATURE CITED
AOU (American Ornithologists' Union). 1998. Check-List of North American Birds. Seventh Edition. American Ornithologists' Union, Washington, D.C. 829 pp.
Bent, A. C. 1942. Life histories of North American flycatchers, larks, swallows, and their allies. U.S. Natl. Mus. Bull. 179. 555 pp.
Blancher, P. J. and D. K. McNichol. 1991. Tree swallow diet in relation to wetland acidity. Canadian Journal of Zoology 69:2629-2637.
Butler, R. W. 1988. Population dynamics and migration routes of tree swallows, Tachycineta bicolor, in North America. J. Field. Ornithol. 59: 395-402.
Doherty, P. F. Jr. and T. C. Grubb Jr. 1998. Reproductive success of cavity-nesting birds breeding under high-voltage powerlines. American Midland Naturalist, 140:122-128.
Finch, D. M. 1990. Effects of predation and competitor interference on nesting success of house wrens and tree swallow. Condor, 92:674-687.
Garrett, K. and J. Dunn. 1981. Birds of Southern California: Status and Distribution. Los Angeles Audubon Society. 407 pp.
Grinnell, J. and A.H. Miller. 1944. The Distribution of the Birds of California. Pacific Coast Avifauna Number 27. Copper Ornithological Club, Berkeley, California. Reprinted by Artemisia Press, Lee Vining, California; April 1986. 617 pp.
Harrison, C. 1978. A field guide to the nests, eggs and nestlings of north American birds. W. Collins Sons and Co., Cleveland, OH. 416pp.
Hays, Loren R. 1999. USFWS, pers. obs.;
Holt, R. F. and K. Martin. 1997. Landscape modification and patch selection: The demography of two secondary cavity nesters colonizing clear-cut. Auk 114:443-455.
Kuerzi, R. G. 1941. Life history studies of the tree swallow. Proc. Linn. Soc. New York 52-53:1-52.
McCaskie, G., P. De Benedictis, R. Erickson, and J. Morlan. 1979. Birds of northern California, an annotated field list. 2nd ed. Golden Gate Audubon Soc., Berkeley. 84pp.
McCaskie, G., P. De Benedictis, R. Erickson, and J. Morlan. 1988. Birds of northern California, an annotated field list. 2nd ed. Golden Gate Audubon Soc., Berkeley. Reprinted with suppl. 108pp.
Moller, A. P. 1991. Clutch size, nest predation and distribution of avian unequal competitors in a patchy environment. Ecology 72:1336-1349.
Muldal, A., H. L. Gibbs and R. J. Robertson. 1985. Preferred nest spacing of an obligate cavity-nesting bird, the tree swallow. Condor 87:356-363.
Patten, Michael. 1998. Riverside County Area for American Field Notes and Past Secretary, California Bird Records Committee, pers. comm.
Pike, James. 1998. USFWS, pers. comm.
Purvis, Richard. 1998. USFWS, pers. comm.
Raphael, M. G., and M. White. 1978. Avian utilization of snags in a northern California coniferous forest. U.S. Dep. Agric., For. Serv., Reg. 5, San Francisco. Prog. Rep. 18pp.
Rennell, W. B. and R. J. Robertson. 1990. Influence of forest edge on nest-site selection by tree swallow. Wilson Bulletin 102:634-644.
Rendell, W. B. and R. J. Robertson. 1994. Defense of extra nest-sites by a cavity nesting bird, the tree swallow. Ardea 82:273-285.
Robertson, R. J., B. J. Stutchbury and R. R. Cohen. 1992. Tree swallow (Tachycineta bicolor) In The Birds of North America, No. 11. (A. Poole and F. Gill, eds.). The Academy of Natural Sciences, Philadelphia, PA and The American Ornithologists' Union, Washington, D.C.
Robertson, R. J. and W. B. Rendell. 1990. A comparison of the breeding ecology of a secondary cavity nesting bird, the tree swallow, in nest boxes and natural cavities. Canadian Journal of Zoology 68:1046-1052.
Sheldon, F. H., and D. W. Winkler. 1993. Intergeneric phylogenetic relationships of swallows estimated by DNA-DNA hybridization. Auk 110: 798-824.
Zarnowitz, J. E., and d. A. Manuwal. 1985. The effects of forest management on cavity-nesting birds in Northwestern Washington USA. J. Wildl. Manage. 49: 255-263.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
tricolored blackbird (Agelaius tricolor) - colony
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
tricolored blackbird (Agelaius tricolor) - colony
Status:
State: Species of Special Concern
Federal: Federal Special Concern species; Partners in Flight Priority Bird Species; Fish and Wildlife Service Migratory Nongame Birds of Management
Other: Audubon Society California Watch List
GROUP DESIGNATION AND RATIONALE
Group 3
The tricolored blackbird occurs in a widely scattered distribution throughout the lowland and foothills Bioregions of the Plan Area. A few current or historic breeding locations have been documented. It has specific Habitat requirements, including patches of dense emergent vegetation as primary Habitat for breeding. It also requires a variety of open Habitats as secondary Habitat and is occasionally known to nest in riparian woodland areas. This species occurs in several Core Areas, including the floodplain of the San Jacinto River, Mystic Lake/San Jacinto Wildlife Area, Collier Marsh, Alberhill, Vail Lake/Wilson Valley/eastern Temecula Creek, and Lake Hemet, which are either currently used or have been used in the past by tricolored blackbird breeding colonies. Although the tricolored blackbird is not documented to occur in the Santa Ana River and Prado Basin in the CNDDB and UCR databases, these areas contain substantial amounts of suitable Habitat and seem likely future or undocumented breeding locations. Because the tricolored blackbird requires specific Habitat conditions, occurs in few locations within a broad Habitat category, and uses a well defined Habitat that is narrowly distributed for its primary Habitat, this species will require site specific considerations, protection of preferred Habitat on a landscape basis, and species-specific conservation measures.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 420 acres of suitable primary Habitat for the tricolored blackbird including freshwater marsh and cismontane alkali marsh Habitats within the Riverside Lowlands and Foothills Bioregions.
Objective 2
Include within the MSHCP Conservation Area the 5 Core Areas, including San Jacinto River floodplain (Proposed Core 5, Existing Constrained Linkage C, Proposed Extension of Existing Core 4, and Proposed Constrained Linkage 19; 7,320 acres), Mystic Lake/San Jacinto Wildlife Area (Existing Core H; 17,470 acres), Collier Marsh and Lake Elsinore grasslands (Subunit 3 of Elsinore Area Plan; 1,810 acres), Alberhill (Subunit 2 of Elsinore Area Plan; 3,460 acres), and Vail Lake/Wilson Valley/eastern Temecula Creek (Proposed Core 7; 50,000 acres).
Objective 3
Include within the MSHCP Conservation Area at least 66,510 acres of secondary Habitat for the tricolored blackbird including playa and vernal pool, grasslands, agriculture land, and riparian scrub, woodland, and forest within the Riverside Lowlands and Foothills Bioregions.
Objective 4
Within the MSHCP Conservation Area, maintain (once every 5 years) the continued use of, and successful reproduction within at least one of the identified Core Areas. Successful reproduction is defined as a nest which fledged at least one known young.
Objective 5
Within the MSHCP Conservation Area, ensure Habitat support functions by maintaining, preserving, and/or if feasible, restoring hydrological processes and Habitat suitable for tricolored blackbird breeding within the San Jacinto River floodplain, Mystic Lake/San Jacinto Wildlife Area, Collier Marsh, Alberhill, and Vail Lake/Wilson Valley/eastern Temecula Creek Core Areas.
Objective 6
Include within the MSHCP Conservation Area and establish a 100-meter buffer around any known nesting locations.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
The tricolored blackbird is frequently an itinerant and opportunistic breeder but is generally associated with wetland Habitat and is identified as preferring emergent vegetation and protected Habitat areas near wetlands for nesting. It may use a wide variety of Habitats, including flooded agriculture lands, pastures, and grasslands in a very nomadic and unpredictable manner for foraging (Garrett and Dunn 1981). The tricolored blackbird also has been documented to use riparian forest Habitats occasionally for nesting. The preferred, or primary, Habitat of the tricolored blackbird includes freshwater marsh and cismontane alkali marsh. Because this species will opportunistically use a relatively wide variety of other Habitats for various parts of the life history, a wide range of Habitats within lowland and foothill Bioregions have been included for this analysis as secondary Habitat. For the purpose of the conservation analysis, potential secondary Habitat for the tricolored blackbird includes playa and vernal pool, riparian scrub, woodland and forest, agriculture lands (field crops) and grasslands. Their nesting Habitat, as identified above may consist of emergent vegetation or other dense well protected vegetation and must be relatively near open foraging Habitat. Suitable areas for nesting and foraging must be large enough to support a large colony of individuals, which have been reported to be as large as 30,000 birds. Based on these Habitats, the Plan Area supports approximately 260,175 acres of potential Habitat for the tricolored blackbird. The Plan Area supports 480 acres of primary Habitat and 259,695 acres of secondary Habitat. Table 1 shows the conservation and loss of potential Habitat for the tricolored blackbird. Overall, approximately 66,935 acres (26 percent) of potential Habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public lands. Approximately 420 acres (88 percent) and 66,515 acres (26 percent) of primary and secondary Habitat will be conserved within the MSHCP Conservation Area, respectively.
TABLE 1
SUMMARY OF HABITAT CONSERVATION FOR
TRICOLORED BLACKBIRD
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| Primary Breeding Habitat in Riverside Lowlands and San Jacinto Foothills Bioregions | |||||||
| Cismontane Alkali Marsh | 10 | 10 | 0 | 10 | 0 | 0 | 0 |
| Freshwater Marsh | 470 | 170 | 240 | 410 | 0 | 60 | 60 |
| Subtotal Primary Breeding Habitat | 480 | 180 (38%) |
240 (50%) |
420 (88%) |
0 | 60 (13%) |
60 (13%) |
| Secondary Foraging or Infrequent Breeding Habitat in Lowland and Foothills Bioregions | |||||||
| Playas and Vernal Pools | 7,870 | 3,830 | 2,880 | 6,710 | 0 | 1,160 | 1,160 |
| Agriculture Land (field crops) | 117,860 | 6,930 | 9,840 | 16,770 | 710 | 100,380 | 101,090 |
| Grassland | 121,750 | 17,470 | 16,130 | 33,600 | 7,000 | 81,150 | 88,150 |
| Riparian Scrub, Woodland, Forest | 12,210 | 3,570 | 5,860 | 9,430 | 180 | 2,600 | 2,780 |
| Subtotal Secondary Foraging or Breeding Habitat | 259,690 | 31,800 (12%) |
34,710 (14%) |
66,510 (26%) |
7,890 (3%) |
185,290 (71%) |
193,180 (74%) |
| TOTAL | 260,170 | 31,980 (12%) |
34,950 (14%) |
66,930 (26%) |
7,890 (3%) |
185,350 (71%) |
193,240 (74%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
The Riparian/Riverine Areas and Vernal Pools Policy described in Section 6.1.2 of the MSHCP, Volume I, provides for conservation through avoidance and minimization of wetlands, which provide Habitat for this species. Mitigation for impacts to wetlands will be incorporated in accordance with the "No Net Loss" policy of federal and state wetland regulations. The proposed mitigation will be directly related to the functions and values of the wetland as related to this species and result in equivalent replacement. This policy is extremely important to providing protection for the nesting Habitat and the Habitats that are used very frequently for foraging by tricolored blackbirds, which include the marshes, playas, mudflats and inundated areas.
Conservation of the tricolored blackbird will be considered from a landscape perspective, as identified above, because the species has specific Habitat requirements for its breeding and foraging areas. Additionally, there are definable locations for focusing conservation efforts where the species is currently known to have a breeding colony or has had breeding colonies in the past. One Core Area (Cooper 2001) is located within the Mystic Lake/San Jacinto Wildlife Area and San Jacinto Floodplain. This Core Area is conserved within Criteria Area and Public/Quasi-Public designations. Areas adjacent to or within these Core Areas, composed of the secondary Habitats of grassland and agriculture lands, are conserved as well. Thus a large contiguous area within the known and recent Core Area is conserved. This species has several other potential or historic Core Areas that are conserved within Criteria Area or Public/Quasi-Public designations including Collier Marsh, Alberhill, and Vail Lake/Wilson Valley/eastern Temecula Creek, which are either used currently or have been used in the past by breeding colonies. A total of 5 Core Areas, including San Jacinto River floodplain (Proposed Core 5, Existing Constrained Linkage C, Proposed Extension of Existing Core 4, and Proposed Constrained Linkage 19; 7,320 acres), Mystic Lake/San Jacinto Wildlife Area (Existing Core H; 17,470 acres), Collier Marsh and Lake Elsinore grasslands (Subunit 3 of Elsinore Area Plan; 1,810 acres), Alberhill (Subunit 2 of Elsinore Area Plan; 3,460 acres), and Vail Lake/Wilson Valley/eastern Temecula Creek (Proposed Core 7; 50,000 acres) will be conserved within the MSHCP Conservation Area. A total of 80,060 acres will be conserved as Core Areas within Criteria Area and Public/Quasi-Public designations. Although the tricolored blackbird has not been documented to be present within the Prado Basin, this area contains substantial amounts of suitable Habitat and seems a likely future or undocumented breeding location and will be conserved within the MSHCP Conservation Area. A total of 9,670 acres within the Prado Basin/Santa Ana River area will be conserved within Criteria Area and Public/Quasi-Public designations.
As described below under Data Characterization, 16 of the 41 recent point localities have a high location precision. Of these 16 point localities, 2 will be inside the Criteria Area or Public/Quasi-Public Lands. The balance of the 14 point localities are located outside the MSCHP conservation area and were recorded in foraging Habitats such as field crops, chaparral, sage scrub, and residential, Habitats not suitable for breeding. These locations, if within a wetland area, will continue to receive protection by the wetland policy of the MSHCP.
Conservation of this species, as a Group 3 species, requires species-specific conservation measures. Species specific objectives identified for the tricolored blackbird include providing protection for the nesting areas by conserving within the MSHCP Conservation Area a 100-meter buffer around any known nesting locations and maintaining (once every 5 years) the continued use of, and successful reproduction within at least one of the identified Core Areas listed above. Successful reproduction is defined as a nest which fledged at least one known young. Additionally, implementation of Objective 6 will ensure the conservation of Habitat support functions within the MSHCP Conservation Area by maintaining, preserving, and/or restoring hydrological processes and Habitat suitable for tricolored blackbird breeding within the San Jacinto River floodplain, Mystic Lake/San Jacinto Wildlife Area, Collier Marsh, Alberhill, and Vail Lake/Wilson Valley/eastern Temecula Creek Core Areas.
MSHCP Conservation Area Configuration Issues
Several large blocks of Habitat supporting the historic breeding locations with currently suitable Habitat, potential nesting colony areas, and potential foraging locations of the tricolored blackbird will be conserved as Criteria Area and Public/Quasi-Public Lands, including the Prado Basin/Santa Ana River, Mystic Lake/San Jacinto Wildlife Area, San Jacinto River floodplain, Vail Lake/eastern Temecula Creek/Wilson Valley, Collier Marsh, and Alberhill. Areas of potential foraging Habitat, including grassland and agriculture land, are including within or adjacent to these areas that are, or have been, identified as breeding colony locations. Other large blocks of Habitat that may provide foraging and nesting opportunities include the Lake Mathews-Estelle Mountain area, Lake Skinner/Diamond Valley Lake area, vernal pools west of Hemet, and the Badlands. Some of these areas contain old or low precision locations of tricolored blackbird and may have been used in the past. Protection of areas associated with wetlands will be provided in Protection of Species Associated with Riparian/Riverine Areas and Vernal Pools policy (Section 6.1.2 of the MSHCP, Volume 1.) This will provide additional protection for the species in protecting nesting and foraging areas associated with wetlands. These MSHCP Conservation Area areas are linked as well, however the tricolored blackbird, due to its ability to move long distances and its nomadic nature, may rely less on Habitat linkages than other species.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 420 acres of suitable primary Conserved Habitat and 66,510 acre of suitable secondary Conserved Habitat and 5 Core Areas within large blocks of Habitat in the MSHCP Conservation Area. The MSHCP Conservation Area will maintain (once every 5 years) the continued use of, and successful reproduction within at least one of the identified Core Areas and will conserve within the MSHCP Conservation Area and establish a 100-meter buffer around any known nesting locations. Implementation of Objective 6 will ensure Habitat support functions within the MSHCP Conservation Area by maintaining, preserving, and/or, if feasible, restoring hydrological processes and Habitat suitable for tricolored blackbird breeding within the San Jacinto River floodplain, Mystic Lake/San Jacinto Wildlife Area, Collier Marsh, Alberhill, and Vail Lake/Wilson Valley/eastern Temecula Creek Core Areas. The current population size of the tricolored blackbird is unknown, however the historic and recent breeding locations are conserved within the MSHCP Conservation Area.
INCIDENTAL TAKE
The Incidental Take of the tricolored blackbird is difficult to quantify due to our limited knowledge of its distribution and abundance within the Plan Area. The maximum level of Incidental Take of tricolored blackbirds can be anticipated by the loss of the number of acres of potential Habitat that will become unsuitable for this species. About 193,240 acres of potential Habitat for the tricolored blackbird will be outside the Criteria Area and Public/Quasi-Public designations, or about 74 percent of the total potential Habitat and individuals within these areas will be subject to Incidental Take consistent with the Plan. Of the primary Habitats, 60 acres will be outside the MSHCP Conservation Area, or about 13 percent of the potential primary Habitat. Of the secondary Habitats, about 193,180 acres will be outside the MSHCP Conservation Area, or about 74 percent of the potential secondary Habitats. It should also be noted that wetland Habitat Areas and Vernal Pools located outside the MSHCP Conservation Area will be subject to the Protection of Species Associated with Riparian/Riverine Areas and Vernal Pools policy presented in Section 6.1.2 of the MSHCP, Volume I. Based on the information from CNDDB, a breeding location is recorded for Lake Hemet. This potential breeding colony site is outside of the MSHCP Conservation Area but within the area subject to protection by the MSHCP Protection of Species Associated with Riparian/Riverine Areas and Vernal Pools policy. A total of 14 of 16 point localities will be located outside the MSCHP Conservation Area, however these point locations were recorded in foraging Habitats such as field crops, chaparral, sage scrub, and residential which are Habitats not suitable for breeding.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The location database for the tricolored blackbird includes 53 records from 1888 to 1999, 41 of which have been recorded since 1990. A total of 16 of these records have a high level of precision and would be accurately located within the Plan Area and are relatively recent. Most of the high precision data records are located within field croplands, non-native grassland, residential areas, within montane areas by Lake Hemet, or at a reservoir. The location of breeding colonies was not available within the UCR database. Additional sources were consulted to identify breeding colonies of the tricolored blackbird including recent Audubon Society records, and CNDDB (Cooper 2001). These sources provided locations and discussions of known breeding areas of the species.
The available literature for the species, documentation of its biology, and the analysis of its locations and population is relatively extensive due to the listing proposal package prepared by Jones & Stokes Associates (Beedy et al. 1991). The literature includes information on locations within the Plan Area as well and management discussions.
Habitat and Habitat Associations
The tricolored blackbird forms the largest colonies of any North American passerine bird. This behavior results in specific Habitat requirements. Breeding colonies may attract thousands of birds to a single site. These colonies require nearby water, a suitable nesting substrate, and open-range foraging Habitat composed of grassland, woodland, or agricultural cropland. In winter, they often form single-species, and sometimes single-sex, flocks, but they also flock with other blackbird species. They often change their nesting locations from year to year. These changes may be an adaptation to exploit rapidly changing environments in ephemeral Habitats, provide secure nesting sites, and provide plentiful insect food supplies (Beedy and Hamilton 1999).
The tricolored blackbird breeds near fresh water, preferably in emergent wetland with tall, dense cattails or tules, but also in thickets of willow, blackberry, wild rose, tall herbs and forages in grassland and cropland Habitats (Ziener et al. 1990). The species seeks cover for roosting in emergent wetland vegetation, especially cattails and tules, and also in trees and shrubs (Zeiner et al. 1990). Although true marsh Habitat with its growth of cattails and tules is favored, marshes are not necessary for the nesting of the species and the species may nest in other protective vegetation including shrubs (Neff 1937). Within the Central Valley of California, the tricolored colonies are generally found in the rice lands of the Sacramento Valley and pasture lands of the lower Sacramento Valley and San Joaquin Valley. The colonies outside the Central Valley are in several different Habitat types including being surrounded by chaparral covered hills which may extend for miles, surrounded by orchard, adjacent to salt marsh, or surrounded by sagebrush-grasslands (Dehaven et al. 1975).
Biogeography
The tricolored blackbird has a relatively restricted range, breeding from southern Oregon and the Modoc Plateau of northeastern California, south through the lowlands of California west of the Sierra Nevada to northwestern Baja California (Grinnell and Miller 1944). The species is not migratory but is nomadic and highly colonial, although the pattern of nomadism is poorly known (Orians 1961). Large flocks appear suddenly in areas from which they have been absent for months, they breed, and then quickly withdraw. This is known as itinerant breeding (Orians 1961; Collier 1968).
The tricolored blackbird is mostly a resident in California (Zeiner et al. 1990). It is common locally throughout the Central Valley and in coastal districts from Sonoma County south (Zeiner et al. 1990). Since 1980, active breeding colonies have been observed in 26 California counties and most of the largest colonies are in the Central Valley (Beedy and Hamilton 1999). It breeds locally west of the Cascade Range, Sierra Nevada, and southeastern deserts from Humboldt and Shasta counties south to extreme southwest San Bernardino County, western Riverside County and western and southern San Diego County. In Central California, its breeding extends east into the foothills of the Sierra Nevada (Beedy and Hamilton 1999). It is a summer resident in northeastern California, occurring regularly only at Tule Lake, but has bred some years as far south as Honey Lake and in the marshes of the Klamath Basin in Siskiyou and Modoc counties (Zeiner et al. 1990). In the southern deserts, it is found regularly only at Antelope Valley, Los Angeles County. In winter, it becomes more widespread along the central coast and San Francisco Bay area (Grinnell and Miller 1944, McCaskie et al. 1979, Garrett and Dunn 1981).
It is not migratory over most of its range, but it leaves Oregon, northeastern California, Santa Barbara County and eastern San Diego County in fall and winter, presumably migrating south (Zeiner et al. 1990; Beedy and Hamilton 1999). Flocks of the species become nomadic in fall, seeking food (Zeiner et al. 1990). In winter, flocks become more widespread from Marin to Santa Cruz counties and in the Sacramento River Delta (Zeiner et al. 1990).
Surveys of the tricolored blackbird indicate that the overall range of the species is little changed since the mid-1930s, however the numbers of the populations have shown a 37 percent decline during a 3-year period from 1994 to 1997. Populations declines are most apparent in the Central Valley of California. Although tricolored blackbirds were once abundant in southern California, they are now described as rare throughout this former range, except in some sections of San Diego County (Beedy and Hamilton 1999).
Known Populations Within Western Riverside County
The early studies (1931 through 1936) of zoologists concluded that no nesting colonies were located within Riverside County (Neff 1937). Later studies within the Plan Area documented one to three breeding colonies comprising 2,000 to 15,750 birds (Dehaven et al. 1975). The historic colonies appear to be located generally in the western portion of the Plan Area, along the Interstate 15 corridor, including Alberhill area and near Temecula (Dehaven et al. 1975). Based on review of the literature, the Temecula location may refer to the eastern portion of Temecula Creek near Vail Lake and east into Wilson Valley and possibly into the Aguanga area.
Tricolored blackbird colonies were first discovered in Riverside County in 1950 and intermittent breeding was reported through the 1980s (Beedy et al. 1991). The largest colony during this time period, at the San Jacinto Wildlife Area, contained 3,000 pairs (4,500 adults) and was extant in 1989. Establishment of this colony contributed an almost 300 percent increase in the regional tricolored breeding population since the 1970s. However, this regional area only comprised about 4 percent of the total tricolored breeding population reported during the 1980s (Beedy et al. 1991). The population within the Plan Area does not appear to be migratory (Garrett and Dunn 1981).
Core areas have been identified as the San Jacinto Valley, considered the floodplain of the San Jacinto River, Mystic Lake/San Jacinto Wildlife Area, based on recent surveys within the Plan Area (Cooper 2001). Other Core Areas that have been important in the past and may continue to provide important core nesting areas include Collier Marsh, Alberhill, and Vail Lake/Wilson Valley/eastern Temecula Creek (Cooper 2001, Dehaven et al. 1975). Based on the information from CNDDB, a breeding location is recorded for Lake Hemet. Other isolated locations of the tricolored blackbird within the UCR database include the Santa Ana River, Lake Mathews, Canyon Lake, Murrieta, Lake Riverside, Hemet, San Jacinto, Lakeview Mountains area, March ARB, Sycamore Canyon Regional park, Badlands, and San Timoteo Creek.
Biology
Genetics: Study of the mitochondrial DNA (cytochrome b) sequences suggested that the nine Agelaius species are a polyphyletic assemblage of ecologically similar species (Lanyon 1994). Red-winged and tricolored blackbirds were found to be sister taxa and in turn these species are sister to the tawny-shouldered blackbird and yellow-shouldered blackbird found in the Caribbean.
Diet and Foraging: The diet of the tricolored blackbird in California consists predominantly of animal matter, mostly insects and spiders, making up 86-91 percent of the nestling and fledgling diet, and 28-96 percent of the adult diet in spring and summer (Skorupa et al. 1980). Insect consumption in the Sacramento Valley reached a peak of 39 percent in summer (Crase and DeHaven 1978). Seeds and cultivated grains, such as rice and oats, are other major foods, and compose most of the fall and winter diet (Martin et al. 1961). The tricolored blackbird forages on the ground in crop lands, grassy fields, flooded land, irrigated pastures, lightly grazed rangelands, dry seasonal pools, mowed alfalfa fields, feedlots, dairies, and along edges of ponds (Zeiner et al. 1990; Beedy and Hamilton 1999).
Daily Activity: The tricolored blackbird exhibits year long, diurnal activity (Zeiner et al. 1990).
Reproduction: The tricolored blackbird usually nests in dense cattails or tules; it also nests in thickets of willow, blackberry, wild rose, and tall herbs (Neff 1937). In the Sacramento Valley, almost 93 percent of the nesting locations were located in freshwater marshes dominated by cattails or bulrushes (Neff 1937). During the more recent years, 53 percent of colonies reported in the Sacramento and San Joaquin Valleys were in cattails and bulrushes (DeHaven et al. 1975). In addition to the freshwater marsh Habitat, nests may be located in a variety of wetland and upland vegetation including blackberries, grainfields, giant cane, safflower, stinging nettles, willow scrub, riparian forest, barley, and orchards (Beedy et al. 1991). Some small breeding colonies may be present at private and public lakes, reservoirs, and parks that may be located near shopping centers, subdivisions and other urban development (Beedy and Hamilton 1999). In general, the characteristics of the nesting locations include: accessible water; protected nesting sites (either flooded or surrounded by thorny or spiny vegetation); and suitable foraging area providing adequate insect prey within a few kilometers of the nesting colony (Beedy and Hamilton 1999).
The nest is usually located a few feet over, or near, fresh water; it also may be hidden on the ground among low vegetation. The tricolored blackbird builds its nest of mud and plant materials (Zeiner et al. 1990). It is a highly colonial species; the nesting area must be large enough to support a minimum colony of about 50 pairs (Grinnell and Miller 1944). The usual breeding season is mid-April into late July (Payne 1969). Orians (1960) also reported active breeding in October and November in Sacramento Valley, although nesting success was low. Individual pairs in breeding colonies may initiate nesting synchronously. Even in colonies of up to 50,000 to 100,000 nests, all first eggs may be laid within one week (Orians 1961). The species is polygynous; each male may have several mates nesting in his small territory (Orians 1961). Tricolored blackbirds are likely itinerant breeders. The evidence for this breeding strategy is documented for a study where in April, all observed tricolored blackbirds were in the vicinity of the breeding colonies then in May and June, populations declined in one area and rose in another as breeding birds moved to the new breeding area (Hamilton 1998).
The clutch size is typically three to four eggs with clutches of two and five eggs observed occasionally (Emlen 1941). The first egg is usually laid the day after the nest is completed, occasionally before; and one egg is laid per day for one to five days (Emlen 1941). They may raise two broods per year (Terres 1980). Incubation lasts about 11 days; the altricial young are tended by the female or by both parents (Lack and Emlen 1939). The young leave the nest at about 13 days (Zeiner et al. 1990). The species probably breeds first at one year (Harrison 1978).
Survival: Although percent nesting success and survival of young has not been determined, the tricolored blackbird has been documented to suffer widespread nest failure, frequently of the entire colony with abandonment of nests with eggs or nestlings (Orians 1961). Abandonment may occur due to a change in the food supply in the area due to drought or timing of nesting or due to harvest activities within the nesting area (Orians 1961).
Dispersal: The tricolored blackbird has frequently been reported to have wholesale desertions of a nesting colony with no obvious destruction or predation of eggs (Lack and Emlen 1939). The abandonment leads to a departure of the entire colony, sometimes to an unknown area of unknown distance (Lack and Emlen 1939).
Socio-Spatial Behavior: Nests may be located up to 6.4 kilometers (4 miles) from foraging areas (Orians 1961). Breeders in Colusa and Yuba counties traveled as far as 6.4 kilometers (4 miles) from the nest to feed; in each of 2 colonies, members foraged over more than 78 kilometers (80 miles) (Orians 1961). The breeding territory, which includes only the vicinity of nest, is usually about 3.3 meters (85 feet), or less, in dense vegetation, but may be larger in less suitable cover (Orians 1961).
Community Relationships: The tricolored blackbird is highly gregarious in all seasons (Collier 1968). Dense breeding colonies are vulnerable to massive nest destruction by mammalian and avian predators, including Swainson's hawks (Bent 1958).
Threats to Species
The population size appears to be declining in California and has fallen more than 72 percent between the 1970s and 1980s largely due to the size of the colonies rather than due to the number of colonies within the range (DeHaven et al. 1975; Beedy et al. 1991). Results of tricolored blackbird observations at Kesterson Reservoir, Colusa National Wildlife Refuge, and the Butte Sink (California) suggest that this species is sensitive to a variety of environmental perturbations while breeding. Predation is a documented source of mortality and this problem may increase as the continued loss of wetlands and other nesting Habitat forces nesting colonies into confined areas. In fact, in 1937, it was concluded that the destruction of nesting Habitats by man is of more importance and that reclamation and drainage have destroyed many favorable Habitats and other Habitats have been destroyed by the dredging or cleaning of reservoirs, marshes, and canals (Neff 1937). Dehaven et al. (1975) found fewer colonies, smaller colonies and an overall smaller population size in California than that documented by Neff (1937). This decline has been attributed to the loss of suitable nesting Habitat for the tricolored blackbird (Dehaven et al. 1975).
A principal factor implicated in the population decline and the loss of individual colonies is elimination of wetland Habitat, which has drastically reduced available nesting and foraging Habitat (Beedy, et al. 1991). The smaller colonies that have resulted from this reduced nesting and foraging Habitat may be more vulnerable to disturbance by natural predators and also less able to compete with other species for the limited wetland nesting Habitat. Higher rates of nesting failures and lower reproductive success have been observed in small colonies compared to large colonies (Orians 1961; Payne 1969).
Poisoning, either deliberate or indirect, and increased disturbance by humans, from agriculture operations such as harvesting, have also been cited as contributing to the continued population decreases (Beedy, et al. 1991). Additionally, contamination by trace elements (selenium) and pesticides are a potential cause of nesting failures (Beedy and Hayworth 1987).
Special Biological Considerations
The tricolored blackbird is intensely gregarious and every major phase of its life is performed in close association with its colony members including the onset of nesting and in some cases, egg laying (Neff 1937). A colony varies in size from a minimum of about 50 nests (Grinnell and Miller 1944) to over 20,000 in an area of 4 hectares (10 acres), or less (DeHaven et al. 1975). Colonies were even larger in former decades. Apparently, the tricolored blackbird has the highest nesting density of any blackbird in North America (Ehrlich et al. 1988).
Population declines of the species have been most apparent in the Central Valley, although tricolored blackbirds were once abundant in southern California. They have been described as rare throughout the area within southern California except in some sections of San Diego County. Recently, observed populations in southern California consist of about 43,000 breeding adults (Beedy and Hamilton 1999). More than half of all the observed nesting efforts throughout the distribution of this species in the 1990s occurred in a few large colonies (Hamilton 1998). These declines can be attributed to the loss of nesting and foraging Habitat throughout the breeding distribution of the species in the Central Valley of California and in southern California (Beedy and Hamilton 1999).
Breeding in autumn occurs infrequently and appears to be entirely dependent upon agricultural and duck-hunting practices. It is likely that fall breeding is of recent origin, postdating irrigation in the area. Rainfall seems to be the most likely factor inducing fall nesting, but the population may have been physiologically prepared some time before the rains came (Orians 1960). Because of favorable conditions for adult blackbirds, fall breeding is likely to confer selective advantage upon those individuals responding to autumnal conditions in spite of the low breeding success typically observed (Orians 1960). Inclusion of late season breeding colonies in estimates of overall abundance would result in substantial overestimates of the global population (Hamilton 1998).
During the breeding season, the species exhibits itinerant breeding (Hamilton 1998). Some individuals move after the first nesting efforts in March to April and small colonies may form from April through June throughout the range. Local and regional declines in the number of breeding tricolored blackbirds of an order of magnitude or more resemble population collapses but probably are attributable to itinerant breeding (Hamilton 1998).
A critical feature of the tricolored blackbird is that it requires a nesting Habitat, frequently in association with a wetland Habitat, that may accommodate many pairs and adequate protection from predation for the nests as well as suitable foraging in the form of more upland Habitat. Breeding individuals may forage away from their nest sites, often well out of sight of the colony. Most of them forage within five kilometers of the colony site but may commute up to 13 kilometers one way (Orians 1961; Beedy and Hamilton 1999).
Management objectives include maintaining a viable, self-sustaining population throughout the current geographic range, avoiding the losses of the colonies and their associated Habitats, increasing the breeding population on suitable public and private lands managed for this species, and enhancing the public awareness and support for protection of Habitat and active colonies (Beedy and Hamilton 1999). Measures have been taken to protect the nesting activities of the tricolored blackbird including purchase of portions of crops to preserve large colonies. These actions and participation by landowners resulted in additions of an estimated 37,000 to 44,000 first-year adults to the 1994 and 1995 breeding seasons. Activities to protect the colony included delaying harvest to avoid the active breeding season. Other activities that results in losses including mowing, plowing, or burning of marsh areas within duck clubs and reservoirs or wetland maintenance of reservoirs containing occupied Habitat. These losses are temporal and could easily be avoided by delaying the activity until after the colony completes the breeding cycle (Beedy and Hamilton 1999).
LITERATURE CITED
Beedy, C. E. and A. M. Hayworth. 1987. Tricolored blackbird nesting failures in the Central Valley of California: General trends or isolated phenomena? In D. Williams (ed.), Proceedings of the conference on the biology, management, and conservation of endangered and sensitive species of the San Joaquin Valley, CA., Bakersfield, CA.
Beedy, C. E., and W. J. Hamilton III. 1999. Tricolored blackbird (Agelaius tricolor). In The Birds of North America, No. 423 (A. Poole and F. Gill, eds.). The Academy of Natural Sciences, Philadelphia, and The American Ornithologists' Union, Washington, D.C.
Beedy, C. E., S. D. Sanders, and P. Bloom. 1991. Breeding status, Distribution, and Habitat Associations of the Tricolored Blackbird (Agelaius tricolor) 1850-1989. Prepared for U.S. Fish and Wildlife Service; In Cooperation With: Jones & Stokes Associates, Inc.
Bent, A. C. 1958. Life histories of North American blackbirds, orioles, tanagers, and allies. U.S. Natl. Mus. Bull. 211. 549pp.
Collier, G. 1968. Annual cycle and behavioral relationships in the red-winged and tricolored blackbirds of southern California. Ph.D. Thesis, Univ. California, Los Angeles. 374pp.
Cooper, D. S. 2001. California Important Breeding Areas. Audubon California. Los Angeles.
Crase, F. T., and R. W. DeHaven. 1978. Food selection by five sympatric California blackbird species. Calif. Fish and Game 64:255-267.
DeHaven, R. W., F. T. Crase, and P. P. Woronecki. 1975. Breeding status of the tricolored blackbird, 1969-1972. Calif. Fish and Game 61:166-180.
Ehrlich, P. R., D. S. Dobkin, and D. Wheye. 1988. The birder's handbook. Simon and Schuster, New York. 785pp.
Emlen, J. T. 1941. An experimental analysis of the breeding cycle of the tricolored red-wing. Condor 43: 209-219.
Garrett, K., and J. Dunn. 1981. Birds of southern California. Los Angeles Audubon Soc. 408pp.
Grinnell, J., and A. H. Miller. 1944. The distribution of the birds of California. Pac. Coast Avifauna No. 27. 608pp.
Hamilton, W. J. 1998. Tricolored blackbird itinerant breeding in California. Condor 100: 218-226.
Harrison, C. 1978. A field guide to the nests, eggs and nestlings of North American birds. W. Collins Sons and Co., Cleveland, OH. 416pp.
Lack, D., and J. T. Emlen, Jr. 1939. Observations on breeding behavior in tricolored red- wings. Condor 41:225-230.
Lanyon, S. M . 1994. Polyphyly of the blackbird genus Agelaius and the importance of assumptions of monophyly in comparative studies. Evolution 48: 679-693.
Martin, A. C., H. S. Zim, and A. L. Nelson. 1961. American wildlife and plants, a guide to wildlife food habits. Dover Publ., Inc., New York. 500pp.
McCaskie, G., P. De Benedictis, R. Erickson, and J. Morlan. 1979. Birds of northern California, an annotated field list. 2nd ed. Golden Gate Audubon Soc., Berkeley. 84pp.
Neff, J. A. 1937. Nesting distribution of the tri-colored red-wing. Condor 39:61-81.
Orians, G. H. 1960. Autumnal breeding in the tricolored blackbird. Auk 77:379-398.
Orians, G. H. 1961. The ecology of blackbird (Agelaius) social systems. Ecol. Monogr. 31:285-312.
Payne, R. B. 1969. Breeding season and reproductive physiology of tricolored and red- winged blackbirds. Univ. Calif. Publ. Zool. 90:1-114.
Skorupa, J. P., R. L. Hothem, and R. W. DeHaven. 1980. Foods of breeding tricolored blackbirds in agricultural areas of Merced County, California. Condor 82:465-467.
Terres, J. K. 1980. The Audubon Society encyclopedia of North American birds. A. Knopf, New York. 1100pp.
Zeiner, D.C., W. F. Laudenslayer, K. E. Mayer and M. White eds. 1990. California's Wildlife: Volume II - Birds. California Department of Fish and Game. Sacramento, California. 732pp.
turkey vulture (Cathartes aura) - breeding
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
turkey vulture (Cathartes aura) - breeding
Status:
State: None
Federal: San Bernardino National Forest Sensitive
GROUP DESIGNATION AND RATIONALE
Group 3
The turkey vulture is generally widely distributed throughout the Plan Area. There are fewer observations within the mountainous Bioregions, however this could be due to lack of survey effort or reporting in these areas. There are concentrations of observation locations within the southwestern portion of the Plan Area from Lake Elsinore to the Santa Rosa Plateau, east to Wilson Valley and Lake Skinner. The focus of this planning effort is on the nesting of the turkey vulture. There are two recorded nest sites within the Plan Area: Bernasconi Hills near Lake Perris and Rawson Canyon near Lake Skinner. Turkey vultures have strict nest-site requirements and few potential sites are located within the Plan Area. Because the turkey vulture requires specific conditions for its nesting location which may occur within a broad variety of Habitats at few locations within the Plan Area, the turkey vulture will require site-specific and species specific considerations and management requirements.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 457,160 acres of suitable foraging Habitat for the turkey vulture including montane coniferous forest, oak woodlands and forests, coastal sage scrub, chaparral, desert scrubs, Riversidean alluvial fan sage scrub, grassland, and playa and vernal pool.
Objective 2
Include within the MSHCP Conservation Area areas where the turkey vulture has been observed and that may function as important foraging locations, including Lake Mathews-Estelle Mountain (Existing Core C plus Proposed Extension of Existing Core 2; 23,710 acres), Sedco Hills (Proposed Linkage 8; 5,470 acres), Lake Skinner/Diamond Valley Lake area (Existing Core C plus Proposed Extension of Existing Cores 5, 6, and 7 and Existing Constrained Linkage A; 29,370 acres), Wilson Valley/Sage (Subunit 2 of REMAP Area Plan; 33,540 acres), Badlands (Proposed Core 3; 24,920 acres), and Prado Basin/Santa Ana River (9,670 acres), and a portion of Santa Rosa Plateau (Existing Core F plus Proposed Linkages 9 and 10, and Proposed Constrained Linkages 9 through 12; 14,130 acres).
Objective 3
Include within the MSHCP Conservation Area, protect, and buffer from disturbance the 2 known nesting locations of the turkey vulture including the site within the Bernasconi Hills (historic) and the site within Rawson Canyon (currently active). Protection is the conservation of undeveloped Habitats in the MSHCP Conservation Area within a 1 mile radius of each nesting location. Buffering of the two known nest sites will include restricting human activities, within the MSHCP Conservation Area, within a 1/2 mile radius around each of the nesting locations during the breeding season (e.g., fencing hiking trails or fencing potential access points).
Objective 4
Within the MSHCP Conservation Area, maintain (once every 3 years) the continued use of, and successful reproduction at the two known nesting locations, and at nesting locations identified in the MSHCP Conservation Area in the future. Successful reproduction is defined as a nest which fledged at least one known young.
Objective 5
Include within the MSHCP Conservation Area cliff areas that are capable of supporting nesting turkey vultures.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
The turkey vulture uses predominantly open hilly Habitats with protected nest and roost sites provided by cliffs, caves, ledges, rock outcrops, large trees, snags, thickets, and shrubs (Coles 1944; Work and Wool 1942; Zeiner, et al. 1990). These Habitats include pastured rangeland, non-intensive agriculture, forest, rocky cliff or slope, deciduous forest, brushy Habitat or grassy Habitat. Observations of the turkey vulture within intensive row-crop agriculture and developed areas, may be of winter migrants or individuals traveling between foraging areas (Thompson, et al. 1990). The turkey vulture breeds in very few locations within the Area Plan, but forages and winters virtually throughout. Two known nest locations exist; One is currently active within Rawson Canyon north of Lake Skinner and the other is historical but probably still suitable within the Bernasconi Hills near Lake Perris. For the purpose of the conservation analysis, potential Habitat for nesting of the turkey vulture includes the Habitat where cliffs, rock outcrops, large trees, or snags required for breeding occur, such as montane coniferous forest (no recorded breeding but may contain cliff sites or large trees suitable for turkey vulture nests), oak woodlands and forests, coastal sage scrub, and chaparral. The species must also have sufficient suitable foraging Habitat to breed successfully which is considered to additionally include desert scrubs, Riversidean alluvial fan sage scrub, grassland, and playa and vernal pool. Agriculture land has not been included because most of the agriculture land is row crops and orchard and although the species may use these periodically, the literature indicates that use is predominantly within the nonbreeding season by migrant turkey vultures. Based on these Habitats, the Area Plan supports approximately 799,520 acres of potential Habitat for the turkey vulture. Table 1 shows the conservation and loss of potential Habitat for the turkey vulture. Overall, approximately 457,160 acres (57 percent) of Habitat in the Area Plan will be conserved in Criteria Area or existing Public/Quasi-Public Lands.
As described above under Data Characterization, 105 of the 219 recent point localities have a high location precision. Of these 105 point localities, 33 will be inside the Criteria Area or Public/Quasi-Public lands. A total of 53 point localities will be outside of the MSHCP Conservation Area and 19 point locations are within the Rural/Mountainous category. Many of these 72 point localities are likely of winter migrants, which are not the focus of the MSHCP Plan. Conservation of this species will be considered from a combination of a landscape perspective, based on the suitable Habitat for the species, specific locations including Core Areas for foraging and specific locations for nesting, and species specific considerations to provide protection for the known nesting areas and protection of select conditions for nesting.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
TURKEY VULTURE
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| All Bioregions | |||||||
| Grassland | 146,870 | 20,010 | 22,810 | 42,820 | 12,220 | 91,830 | 104,050 |
| Playas and Vernal Pools | 7,910 | 3,830 | 2,920 | 6,750 | 0 | 1,160 | 1,160 |
| Desert Scrubs | 9,360 | 3,670 | 1,310 | 4,980 | 40 | 4,340 | 4,380 |
| Riversidean Alluvial Fan Sage Scrub | 7,150 | 3,170 | 2,060 | 5,230 | 220 | 1,700 | 1,920 |
| Oak Woodlands and Forests | 32,180 | 2,390 | 20,500 | 22,890 | 5,020 | 4,270 | 9,290 |
| Montane Coniferous Forest | 29,890 | 20 | 20,480 | 20,500 | 40 | 9,350 | 9,390 |
| Coastal Sage Scrub | 152,690 | 47,160 | 34,560 | 81,720 | 26,240 | 44,730 | 70,970 |
| Chaparral | 413,470 | 64,900 | 207,370 | 272,270 | 59,580 | 81,620 | 141,200 |
| TOTAL | 799,520 | 145,150 (18%) |
312,010 (39%) |
457,160 (57%) |
103,360 (13%) |
239,000 (30%) |
342,360 (43%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
Core areas where the turkey vulture has been observed and that may function as important foraging locations will be conserved within the MSHCP Conservation Area. These Core Areas include Lake Mathews-Estelle Mountain (Existing Core C plus Proposed Extension of Existing Core 2; 23,710 acres), Sedco Hills (Proposed Linkage 8; 5,470 acres), Lake Skinner/Diamond Valley Lake area (Existing Core C plus Proposed Extension of Existing Cores 5, 6, and 7 and Existing Constrained Linkage A; 29,370 acres), Wilson Valley/Sage (Subunit 2 of REMAP Area Plan; 33,540 acres), Badlands (Proposed Core 3; 24,920 acres), and Prado Basin/Santa Ana River (9,670 acres), and a portion of Santa Rosa Plateau (Existing Core F plus Proposed Linkages 9 and 10, and Proposed Constrained Linkages 9 through 12; 14,130 acres). A total of 140,810 acres of Core Areas are conserved within the Criteria Area or Public/Quasi-Public Lands.
The two known or historic nest locations, Rawson Canyon and the south side of Lake Perris (Bernasconi Hills) are conserved within the Criteria Area or Public/Quasi-Public Lands. These nest locations also will be provided a buffer from disturbance. Protection of these nest locations includes the conservation of undeveloped Habitats within the MSHCP Conservation Area within a 1 mile radius of each nesting location. Buffering of the nest sites will include restricting human activities within a 1/2 mile radius around each of the nesting locations during the breeding season (e.g., fencing hiking trails or fencing potential access points). To provide additional potential nesting locations within the Area Plan for the turkey vulture, cliff areas that are capable of supporting nesting turkey vultures will be conserved within the MSHCP Conservation Area.
Finally, the conservation of the turkey vulture will include the objective to maintain (once every 3 years) the continued use of, and successful reproduction at the two known nesting locations, and at nesting locations identified in the MSHCP Conservation Area in the future. Successful reproduction is defined as a nest which fledged at least one known young.
Rural/Mountainous
As depicted on the MSHCP Plan Map (Figure 3-1, MSHCP Volume I), certain areas adjacent to or in proximity of the MSHCP Conservation Area are designated as Rural/Mountainous in the County's General Plan. These areas are generally constrained for development due to steep topography and the level of development in these areas is anticipated to be of a low density, rural residential character. These areas will not be included within the MSHCP Conservation Area or managed for the benefit of species conserved under the MSHCP, and the existing zoning/ordinances for these areas do not preclude development and could allow substantial fragmentation and/or degradation of Habitat for proposed covered species. However, the low levels of development anticipated in these areas may provide a buffer to the MSHCP Conservation Area that may be of value to certain species including the turkey vulture. Conservation of the Santa Rosa Plateau and the area north of Sage is important for providing foraging Habitat. MSHCP Conservation Area locations in these areas are generally surrounded by Rural/Mountainous designations. Potential development in these areas is anticipated to retain vacant areas that may provide for foraging opportunities for this species. A total of 103,360 acres (13 percent) of potential Habitat will be designated Rural/Mountainous.
MSHCP Conservation Area Configuration Issues
Several large blocks of Habitat supporting the current known and potential foraging and nesting locations of the turkey vulture will be conserved as criteria area and Public/Quasi-Public designations, including Rawson Canyon and the Bernasconi Hills area. Within the Bernasconi Hills, approximately 2,500 acres of coastal sage scrub and rocky hill are conserved with adjacent grassland for foraging. Within the Rawson Canyon area, the entire canyon, as well as the surrounding chaparral and coastal sage scrub, encompassing at least 2,000 acres is conserved. Additional locations which may contain nest sites and contain potential and known foraging Habitat include portions of the Santa Rosa Plateau, Vail Lake/Wilson Valley, Lakeview Mountains, Lake Mathews-Estelle Mountain, Lake Skinner/Diamond Valley Lake area, Sage, Aguanga, Badlands, Sedco Hills, Prado Basin/Santa Ana River, and forested areas within the Cleveland and San Bernardino national forests. As identified above, the species breeds and winters within the Area Plan and as such, the MSHCP Conservation Area will provide adequate Habitat for nesting and year-round foraging.
Special conservation measures specific to the turkey vulture include protection of nest sites from human disturbance during the nesting season. No known methods for protecting turkey vulture nests have been documented, however methods have been developed for the peregrine falcon which also is sensitive to human disturbance. Thus, the following are taken from the peregrine falcon recovery plan and provide the best known available protection for a similarly sensitive bird species: (1) Prohibit land-use practices and/or development that will adversely alter or eliminate existing Habitat within one mile of the nesting cliff or site; (2) Prohibit human activities within one-half mile distance of the nest site between February 1 and September 1 of each year; and (3) Prohibit land-use practices and/or developments which could alter or eliminate the character of the foraging Habitat or food source within the area of the nest site. Sites suitable for occupancy and/or expansion will be protected and managed accordingly to ensure that the quality of the Habitat is not altered or eliminated.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 457,160 acres of suitable Conserved Habitat and 140,810 acres of Core Areas within large blocks of Habitat in the MSHCP Conservation Area. The two known nesting locations will be conserved within large blocks of Habitat within the MSHCP Conservation Area and the nest locations will be buffered from disturbance. Additional cliff areas for potential nesting also will be included within the MSHCP Conservation area. In addition, Objective 4 will maintain (once every 3 years) the continued use of, and successful reproduction at the two known nesting locations, and at any nesting locations identified in the MSHCP Conservation Area in the future.
INCIDENTAL TAKE
The Incidental Take of the turkey vulture is difficult to quantify due to our limited knowledge of its distribution and abundance within the Plan Area. The maximum level of Incidental Take of turkey vultures can be anticipated by the loss of the number of acres of Habitat that will become unsuitable for this species. About 342,360 acres (43 percent) of potential Habitat for the turkey vulture will be outside the Criteria Area and Public/Quasi-Public designations and individuals within this Habitat will be subject to Incidental Take consistent with the Plan. A total of 53 point localities will be outside of the MSHCP Conservation Area and 19 point locations are within the Rural/Mountainous category. Many of these 72 point localities are likely of winter migrants, which are not the focus of the MSHCP Plan. Both of the nesting locations are within conserved areas. Some of the foraging area within which there are a concentration of point locations will not be conserved within the Santa Rosa Plateau.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The location database for the turkey vulture includes 273 records dated from 1900 to 1999. Nest record locations are from collections of eggs from approximately 1900 to 1908 within the Bernasconi Hills south of Lake Perris and one recent record for Rawson Canyon (Bloom 2002 pers. comm.). There is no additional recent nesting information and most of the records are likely from observation of foraging individuals or individuals flying overhead. Approximately 219 records are relatively recent, within the past 10 years. Of these records, approximately 105 are high precision locations and are associated with a wide variety of native and non-native Habitats including chaparral, sage scrub, grassland, riparian, coniferous forest, open water, upland forest, orchard, residential, crop lands, dairy feed yard, oak woodlands, and others.
A moderate amount of literature is available for the turkey vulture because it is a bird of prey. Most of the literature pertains to general natural history, however less is known about this species than many raptor species. Few controlled scientific studies have been conducted, however some management studies are available. Very little information is available for the Area Plan other than what is available regarding basic distribution information.
Habitat and Habitat Associations
The preferred Habitat of the turkey vulture in eastern North America includes mixed farmland and forest, which provides the best opportunity for foraging on both wild and domestic carrion. For nesting in this region, it prefers forested or partly forested areas with nest sites such as rock outcrops, fallen trees, and abandoned buildings that are isolated from human and perhaps other mammalian disturbance (Kirk and Mossman 1998). For communal roosting, the turkey vulture prefers stands of large trees free from human disturbance. Also preferred, are hilly areas that provide deflective updrafts for flight, especially in the north, where thermals may be weak and unpredictable. It avoids extensive areas of row-crop farmland. The preferred areas are best found in swampy areas or hilly, often unglaciated uplands with low-input agriculture (Coleman and Fraser 1989a).
In the west, it tends to occur most regularly in areas of pastured rangeland, non-intensive agriculture, or wild areas, with rock outcrops suitable for nesting but generally not in the high mountains. Suitable Habitat for the species consists of extensive open areas with protected nest and roost sites provided by large trees, snags, thickets, shrubs, and rock outcrops (Zeiner, et al. 1990). The species occurs in open stages of most Habitats that provide adequate cliffs or large trees for nesting, roosting, and resting (Garrett and Dunn 1981). The turkey vulture uses large trees, rock outcrops, and riparian thickets for roosting, perching, and sunning (Hatch 1970). Turkey vulture nesting Habitat may occur in forest, rocky cliff or slope, deciduous forest, brushy Habitat or grassy Habitat. Turkey vultures roost communally during the winter and roost sites contain large conifers that are near Habitat features that contribute to air currents (Thompson, et al. 1990).
Biogeography
The turkey vulture breeds in north to southern British Columbia, northern Idaho, northwestern Montana, east-central Alberta, west-central Saskatchewan, southern Manitoba, western Ontario, southern Quebec, western Vermont, southern New Hampshire, and the southern half of Maine, south through the continental United States, Middle America, and South America to Tierra del Fuego and the Falkland Islands. Within the Western United States and western Canada, the breeding range is discontinuous. Breeding is very local or absent in the portions of the Great Plains, including most of Nebraska, eastern Colorado, and much of western Kansas (Kirk and Mossman 1998).
It winters primarily from northern California and north Central Valley south to the Mexican border, lower Colorado River Valley north to Parker, Arizona, New Mexico, eastern half of Texas, southeastern Oklahoma, through the southern portions of the mid-western states, north West Virginia, southeastern Pennsylvania, southern New York and southern Connecticut (Kirk and Mossman 1998). The turkey vulture is a partial migrant and individuals that breed north of the wintering range are generally migratory. They may be nomadic along the northern border of the winter range (Kirk and Mossman 1998).
Beginning in the 1920s and continuing to the 1990s, in the upper Midwest, the breeding range has expanded northward. The populations has increased markedly in the northern parts of the range of the turkey vulture where it formerly bred only sparingly (Kirk and Mossman 1998).
The turkey vulture is common in the breeding season throughout most of California (Grinnell and Miller 1944). It is absent to uncommon in most of the state in winter, with the greatest concentrations in coastal regions and is not found at the highest elevations in Sierra Nevada. It migrates south or downslope for winter. Some individuals, occurring in coastal regions, winter in California. The remainder of the population migrates, mostly to Central America, for the winter (Grinnell and Miller 1944). Large flocks concentrate along well defined, traditional migration routes in the autumn (Garrett and Dunn 1981).
Known Populations Within Western Riverside County
The turkey vulture is considered a year round resident throughout western Riverside county (Zeiner et al. 1990). The turkey vulture is widely distributed throughout the Area Plan especially within the central portion but also has scattered observation locations within the montane areas. It is considered a relatively common spring and fall transient or migrant and an uncommon year round resident (Garrett and Dunn 1981). There are concentrations of observation locations within the southwestern portion of the Area Plan from Lake Elsinore to the Santa Rosa Plateau, east to Wilson Valley and Lake Skinner. There are also a number of locations within the Moreno Valley, into the Badlands and to Beaumont. There are no breeding records for the Area Plan from the literature, however they have been documented anecdotally as nesting in cliff areas at Rawson Canyon and Lake Perris (Bernasconi Hills). The Bernasconi Hills nesting record is from approximately 1900 and although this record is very old, the location may still be a likely nesting location. A second nest record is for Rawson Canyon near Lake Skinner is a recent and active location (Bloom 2002 pers. comm.).
Biology
Genetics: The results of the genetic studies of the storks, Ciconiidae, show the family includes outgroups from the New World vultures, Cathartidae and ibises and spoonbills, Threskiornithidae (Slikas 1997). Phylogenetic analysis based on syringeal morphology and re-analysis of DNA-DNA hybridization data support inclusion of cathartids with Falconiformes (Griffiths 1994). Subspecific taxonomy of the turkey vulture is based on poorly defined average differences in size (wing and tail length) and coloration, including plumage and bare skin of head and neck. As many as six subspecies are recognized, depending on the authority (Kirk and Mossman 1998).
Diet and Foraging: The turkey vulture primarily eats wild and domestic carrion; rarely eats rotting fruit, live birds, eggs, or live mammals (Zeiner, et al. 1990). Mammals are the most common food item, ranging from mice and shrews to large ungulates; birds include mostly chickens; and the species is very adaptable to the local and regional variety of available carrion. The relative use of wild versus domestic, mammal versus non-mammal, and large versus small food items varies considerably (Hiraldo, et al. 1991). The diversity and distribution of taxa constituting food items show turkey vultures to be opportunistic scavengers covering a variety of local Habitats (Tomaides, et al. 1989). It is a highly specialized static soarer, foraging aerially over roads, fields, open forests, and nearly all open Habitats (Zeiner, et al. 1990). This species searches for carrion from the air and from a perch, aided by its sense of smell, which is well developed in the species (Smith and Paselk 1986). It may rob food from young herons and possibly other species (Temple 1969). It generally feeds on the ground and may wade into shallow water to fish or to feed on carcasses. Sometimes it lands on floating carcasses. The turkey vulture eats its food almost entirely where it is found or drags it off a few meters. It may fly a short distance with the food in its bill, especially if it is live prey and small enough to carry (Kirk and Mossman 1998).
Daily Activity: The turkey vulture exhibits year-long, diurnal activity (Zeiner, et al. 1990). On windy mornings, it may leave the communal roost to forage as early as 0.5 hour before sunrise, but usually stays in the roost area exposed to the sun where it engages in maintenance activities. It typically leaves to forage as air currents develop 1 to 5 hours after sunrise, but may stay on the roost or post-roosting area all day in the rain. Usually it returns to the roost 1 to 3 hours before sunset (Kirk and Mossman 1998).
Reproduction: Cliffs, rock outcrops with rims, caves, ledges, and cavities in trees, snags, and logs are used for nesting by the turkey vulture (Coles 1944; Work and Wool 1942). The most important requirement of the nest site appears to be isolation from human disturbance. The size and shape of nest cavities is variable and difficult to categorize however the cavities are frequently too constricted or convoluted for entry by a human (Kirk and Mossman 1998). A ritualized display including several individuals may precede mating (Loftin and Tyson 1965, Brown and Amadon 1968). The turkey vulture lays 1 clutch per year of 2 eggs, rarely 1 or 3 (Work and Wool 1942). It incubates the eggs for 38-41 days (Brown and Amadon 1968). The semialtricial young hatch with eyes open; they are cared for by both parents for 80 days, or more (Work and Wool 1942). Breeding birds have a strong fidelity to the breeding site. Marked birds are known to return to the same or nearby alternate nest for six or more years and no birds tagged as nesting adults have ever been reported during the nesting season of subsequent years at a location greater than 10 kilometers from the original nest (Kirk and Mossman 1998).
Survival: Annual survival of the turkey vulture is at least 75 percent on the basis of nine radio tagged vultures (Coleman and Fraser 1989b). The longevity record is 17+ year (Clapp et al. 1982).
Dispersal: There are few data regarding dispersal of the turkey vulture. The immatures tend to wander during the second summer or return late in the season. Birds were equally or more likely to return to the natal area for the first time in the third year than in the second year; all birds that returned to the natal area in the second year did so after June (Kirk and Mossman 1998).
Socio-Spatial Behavior: No data were found, but observations indicate turkey vulture uses extensive areas (Zeiner et al. 1990). Individuals regularly forage out 24-32 kilometers (15-20 miles) from the roost or nest. There is little evidence of territoriality found however the nest locations are well spaced from each other (Zeiner et al. 1990; Coleman and Fraser 1989a). In California, as many as 500 juveniles have been observed using communal roosts August through October (Grinnell and Miller 1944). The species appears to have a large home range, which is typically overlapped with that of other individuals. In eastern North America, the home range size was 27,050 hectares in the summer, 12,773 hectares in the winter and 37,072 hectares year-round (Kirk and Mossman 1998). In a study using radio tagged turkey vultures, their home range was reported to be 37,072 hectares (Coleman and Fraser 1989a).
Community Relationships: The turkey vulture often feeds with ravens and condors, although apparently it is subordinate to each (Bent 1937). Golden eagles and coyotes may keep turkey vultures from carcasses. There is no evidence that communal roosting acts as an information-center; that is, those turkey vultures that return to bait sites do not act as leaders for groups of naive birds (Buckley 1997).
Threats to Species
Human disturbance and canid predation may be significant causes of nest failure (Coleman and Fraser 1989a). Other threats include shooting, trapping, and poisoning; pesticide and other contaminants or toxics including DDT, DDE, lead poisoning, and mercury contamination; collisions with stationary or moving structures or objects (Kirk and Mossman 1998).
A 50 percent decline in the roosting population of the turkey vulture in Oregon has been hypothesized to be partially or wholly attributed to the overall regional decline of the species, to the unlikely use of new roost site or to changing land use practices which have reduced the availability of carrion in the form of range cattle (Taylor 1985).
Special Biological Considerations
Important behavioral mechanisms of the thermoregulatory repertoire for dealing with air temperatures greater than 40 degrees C include neck extension, wing spreading, and urohydrosis, urination on the legs (Hatch 1970; Arad and Bernstein 1988).
The population size and nest densities are difficult to assess because of the wide daily range, the clumped distribution around the communal roosts, unknown geographic area covered by birds counted at the roosts, and unknown proportions of local populations breeding (Kirk and Mossman 1998).
Turkey vultures may roost in communal groups during the winter (Thompson et al. 1990). Studies on Habitat and nesting concluded that vulture numbers can be managed by manipulation of roost, nest, and feeding site quantity and quality (Coleman and Fraser 1989a). Specifically this study found that the home range contains a greater proportion of roads and open Habitat, that they use forested Habitats more than expected for all behaviors except feeding, that Habitat used for perching and nest sites contains no human structures, Habitat used for nest sites was roadless, forested, and undeveloped, nest sites were all in rock crevices and successful nests were farther from buildings than were unsuccessful nests.
Although the species may use roadless areas preferentially for nesting, they appear to establish their home range in areas with greater road densities for use for foraging, probably because of the increase in carrion availability (Trombulak and Frissell 2000).
During the 1960s and 1970s, the North American continental summer population was stable but shifted geographically, with local and regional declines in the southern and western United States (Brown 1976). During the period from 1980 to 1994, there was an expansion and growth of the northern populations and summer populations increased in many other areas. The mechanisms of population regulation are unknown, however the available evidence suggests the following five factors as potentially limiting: food availability - the species is known to disappear from areas when pastured livestock or small farms are replaced by cash crops, there may be an increased availability of road-killed animals concomitant with the increases in vehicular use of roads and this may contribute to range expansion; nest-site availability - apparently a high proportion of the summer population does not breed; predation - evidently fairly common on eggs and hatchlings when the nests are relatively accessible, which is related to the availability of safe and inaccessible nest sites; persecution - thousands have been trapped or shot; chemical contamination - known to occur and to have reached levels sufficient to affect reproduction in the past (Kirk and Mossman 1998).
To enhance turkey vulture populations, more traditional farming practices may be beneficial (Kirk, et al. 1996), including establishing smaller fields, mixed farming with pasture and retention of wood lots or forest tracts with large cavity and roost trees. The turkey vulture should be viewed as almost entirely beneficial, removing tons of animal carcasses from the countryside. Where problems occur with turkey vultures concentrating their activities close to birthing livestock, farmers could remove afterbirths and dead young away from the vicinity of the farm to forested areas (Coleman and Fraser 1987).
LITERATURE CITED
Arad, Z., and M. H. Bernstein. 1988. Temperature regulation in turkey vultures. Condor 90: 913-919.
Bent, A. C. 1937. Life histories of North American birds of prey. Part 1. U.S. Natl. Mus. Bull. 167. 409pp.
Bloom, P. 2002. Pers. Comm.
Brown, W. H. 1976. Winter population trends in black and turkey vultures. American Birds 30: 909-912.
Brown, L., and D. Amadon. 1968. Eagles, hawks and falcons of the world. 2 Vols. Country Life Books, London. 945pp.
Buckley, N. J. 1997. Experimental tests of the information-center hypothesis with black vultures (Coragyps atratus) and turkey vultures (Cathartes aura). Behavioral Ecology and Sociobiology 41: 267.
Clapp, R. B., M. K. Klimkiewicz, and J. H. Kennard. 1982. Longevity records of North American birds: Gavidae through Alcidae. J. Field Ornithol. 53: 81-124.
Coles, V. 1944. Nesting of the turkey vulture in Ohio caves. Auk 61:219-228.
Coleman, J. S., and J. D. Fraser. 1987. Food habits of black and turkey vultures in Pennsylvania and Maryland. J. Wildl. Management 51: 733-739.
Coleman, J. S., and J. D. Fraser. 1989a. Habitat use and home ranges of black and turkey vultures. J. Wildlife Management 53: 782-792.
Coleman, J. S. And J. D. Fraser. 1989b. Age estimation and growth of Black and turkey vultures. J. Field Ornithology 60: 197-207.
Garrett, K., and J. Dunn. 1981. Birds of southern California. Los Angeles Audubon Soc. 408pp.
Griffiths, C. S. 1994. Monophyly of the Falconiformes based on syringial morphology. Auk 111: 787-805.
Grinnell, J., and A. H. Miller. 1944. The distribution of the birds of California. Pac. Coast Avifauna No. 27. 608pp.
Hatch, D. E. 1970. Energy conserving and heat dissipating mechanisms of the turkey vulture. Auk 87:111-124.
Hiraldo, F., M. Delibes, and J. A. Donazar. 1991. Comparison of diets of Turkey Vultures in three regions of northern Mexico. J. Field Ornithol. 62: 319-324.
Kirk, D. A. And M. J. Mossman. 1998. Turkey Vulture (Cathartes aura). In The Birds of North America, No. 339 (A. Poole and F. Gill, eds.). The Academy of Natural Sciences, Philadelphia, and The American Ornithologists' Union, Washington, D.C.
Kirk, D. A., M. D. Evenden, and P. Minear. 1996. Past and current attempts to evaluate the role of birds as predators of insect pests in temperate agriculture. Curr. Ornithol 13: 175-264.
Loftin, H., and E. L. Tyson. 1965. Stylized behavior in turkey vulture courtship dance. Wilson Bull. 77:193.
Slikas, B. 1997. Phylogeny of the avian family Ciconiidae (Storks) based on cytochrome b sequences and DNA-DNA hybridization distances. Molecular Phylogenetics and Evolution 8: 275-300.
Smith, S. A., and R. A. Paselk. 1986. Olfactory sensitivity of the turkey vulture (Cathartes aura) to three carrion-associated odorants. Auk 103: 586-592.
Taylor, D.M. 1985. Turkey vultures decline at a traditional roosting site. Great Basin Naturalist 46:305-306.
Temple, S. A. 1969. A case of turkey vulture piracy on great blue herons. Wilson Bull. 81:94.
Thomaides, C., R. Valdez, W. H. Reid, and R. J. Raitt. 1989. Food habits of turkey vultures in West Texas (USA). J. of Raptor Research 23: 42-44.
Thompson, W. L., R. H. Yahner, and G. L. Storm. 1990. Winter use and Habitat characteristics of vulture communal roosts. J. Wildlife Management 54: 77-83.
Trombulak, S. C., and C. A. Frissell. 2000. Review of ecological effects of roads on terrestrial and aquatic communities. Conservation Biology 14: 18-30.
Work, T. H., and A. J. Wool. 1942. The nest life of the turkey vulture. Condor 44:149-159.
Zeiner, D.C., W. F. Laudenslayer, K. E. Mayer and M. White eds. 1990. California's Wildlife: Volume II - Birds. California Department of Fish and Game. Sacramento, California. 732pp.
western yellow-billed cuckoo (Coccyzus americanus occidentalis)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
western yellow-billed cuckoo (Coccyzus americanus occidentalis)
Status:
State: Endangered
Federal: Partners in Flight Priority Bird Species; Federal Candidate for Listing as Threatened or Endangered; Fish and Wildlife Service Region 1 Species of Management Concern; San Bernardino National Forest Sensitive; Cleveland National Forest Sensitive
Other: Audubon Society Blue List
GROUP DESIGNATION AND RATIONALE
Group 3
The western yellow-billed cuckoo occurs as a breeding bird in only one known location within the Plan Area. It has been recently documented in two other locations but breeding is not confirmed. Although the preferred Habitat, riparian scrub and forest, is well distributed at scattered locations within the Plan Area in the lowland Bioregions, the western yellow-billed cuckoo apparently no longer inhabits much of this Habitat. The western yellow-billed cuckoo has specific narrow Habitat requirements and conditions within the larger Habitat category within which it occurs. Because it requires specific conditions (including broad tracts of suitable riparian Habitat), occurs in few locations within a large Habitat category, and occurs in low densities, the western yellow-billed cuckoo will require conservation on a landscape level to preserve the suitable Habitat, site specific considerations for the known locations, and species specific management conditions.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 8,970 acres of suitable Habitat for the western yellow-billed cuckoo including southern cottonwood/willow riparian, riparian scrub, riparian forest, and southern willow scrub.
Objective 2
Include within the MSHCP Conservation Area at least five Core Areas and interconnecting linkages. Core areas shall include the following areas: 1) Prado Basin/Santa Ana River, including Chino Creek, Mill Creek, and the Santa Ana River both up- and downstream of the Prado Dam (9,670 acres); 2) Temescal Wash including Alberhill Creek (estimated as subunit 3 of Temescal Canyon Area Plan plus Proposed Constrained Linkage 6 and Proposed Linkage 2; 4,290 acres); 3) Murrieta Creek (Proposed Constrained Linkage 13; 1,400 acres); 4) Temecula Creek (Proposed Constrained Linkages 14 and 24; 830 acres); 5) San Timoteo Canyon (Proposed Linkages 5, 12 and Proposed Linkage 22; 2,140 acres). Each Core Area will include at least 100 meters of undeveloped landscape adjacent to the riparian woodland and scrub Habitat and contain unfragmented Habitat and landscape linkages to other Core Areas. The Core Areas must support a population of 20 pairs of cuckoos combined total.
Objective 3
Within the MSHCP Conservation Area, maintain or, if feasible, improve the riparian Habitats within the recent documented locations of the western yellow-billed cuckoo at the Prado Basin, Santa Ana River, North Peak Conservation Bank and Poorman Reservoir. Additionally, maintain or, if feasible, improve the potential yellow-billed cuckoo Habitat (including potential core and other areas) and potential Habitat linkages within the riparian areas along the Santa Ana River both upstream and downstream from Prado Dam, Temescal Wash including Alberhill Creek, Wasson Canyon, Murrieta Creek, Temecula Creek, Vail Lake, Wilson Valley, Bautista Creek, Tucalota Creek, Lake Skinner, Potrero Creek, and San Timoteo Canyon. The maintenance or improvement of Habitat at all locales will be accomplished by preserving the hydrological processes within the drainages that support the potential Habitat and, if feasible, by selectively restoring, rehabilitating or revegetating all such areas that are currently fragmented or otherwise degraded by, for instance, infestations of exotic plants and animals. Each Reserve manager responsible for a Core Area identified above will evaluate the condition of the riparian vegetation within the Core Area and implement a program to maintain or, if feasible, restore, and/or create riparian Habitat within the Core Area. The Riparian/Riverine Areas and Vernal Pools (Section 6.1.2) and Guidelines Pertaining to Urban/ Wildlands Interface (Section 6.1.4) will be implemented within the MSHCP Conservation Area.
Objective 4
Include within the MSHCP Conservation Area additional areas within the Criteria Area identified as important to the western yellow-billed cuckoo. This Objective shall be met through implementation of the Riparian/Riverine Areas and Vernal Pools Policy presented in Section 6.1.2 of the MSHCP, Volume I. Wetland mapping assembled as part of that policy shall be reviewed as part of the project review process and if suitable western yellow-billed cuckoo Habitat, defined as cottonwood or willow riparian Habitat adjacent to flowing water or saturated soils, is identified on the wetland maps and cannot be avoided, a focused survey for western yellow-billed cuckoo shall be conducted by a qualified biologist in accordance with accepted protocols. If survey results are positive, 100 percent of the occupied portions of the property that provide for long-term conservation value for the cuckoo shall be conserved in a manner consistent with conservation of the cuckoo. This will involve including 100 meters of undeveloped landscape adjacent to the Habitat conserved.
Objective 5
Within the MSHCP Conservation Area, maintain (once every 3 years) the continued use of, and successful reproduction at 75 percent of the known western yellow-billed cuckoo occupied Core Areas (including any nesting locations identified in the MSHCP Conservation Area in the future). Successful reproduction is defined as a nest which fledged at least one known young.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
For the purpose of the conservation analysis, potential Habitat for the western yellow-billed cuckoo includes southern cottonwood/willow riparian, riparian scrub, riparian forest, and southern willow scrub within lowland and foothill Bioregions and excludes tamarisk scrub, arundo/riparian forest, montane riparian forest, and mule fat scrub Habitat. Although the cuckoo is probably more restrictive than this in its Habitat use, based on its current distribution, the inclusion of areas not currently occupied within the MSHCP Conservation Area provides the potential for re-occupation of areas that were used historically. The preferred Habitat of the western yellow-billed cuckoo has been analyzed as closely as possible but includes more than the strict dense riparian that they prefer due to the limitations of the vegetation mapping. Given these requisites and caveats, the Plan Area supports approximately 11,550 acres of potential Habitat for the western yellow-billed cuckoo. Table 1 shows the conservation and loss of potential Habitat for the western yellow-billed cuckoo. Overall, approximately 8,970 acres (78 percent) of potential Habitat in the Plan Area will be conserved within the Criteria Area or existing Public/Quasi-Public Lands.
TABLE 1
SUMMARY OF HABITAT CONSERVATION FOR
WESTERN YELLOW-BILLED CUCKOO
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| Riverside lowland and San Jacinto Foothills Bioregions | |||||||
| southern cottonwood/willow riparian, riparian scrub, riparian forest, and southern willow scrub | 11,550 | 3,150 | 5,820 | 8,970 | 160 | 2,420 | 2,580 |
| TOTAL | 11,550 | 3,150 (27%) |
5,820 (51%) |
8,970 (78%) |
160 (1%) |
2,420 (21%) |
2,580 (22%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
In addition, the Riparian/Riverine Areas and Vernal Pools policy described in Section 6.1.2 of the MSHCP, Volume I, provides for conservation of wetlands which will protect some Habitat for this species through avoidance and minimization. Mitigation for impacts to wetlands shall be incorporated in accordance with the "No Net Loss" policy of federal and state wetland regulations. The proposed mitigation shall be directly related to the functions and values of the wetland as related to this species and result in equivalent replacement.
As described above, conservation of the western yellow-billed cuckoo is considered from a landscape perspective in order to provide potentially suitable Habitat within lowland areas. As described below under Data Characterization, there are two relatively recent point localities with high precision within the UCR Database. Of these two point localities, one is located within Public/Quasi-Public Lands, and one is located outside of the MSHCP Conservation Area. The one high precision point located outside the MSHCP Conservation Area is located in field croplands according to the UCR database, however the CNDDB description of this database location is that it is within the Santa Ana River within dense riparian Habitat. This location may be a registration error or it was observed near field crops but the mapping is not able to place it with great accuracy in the proper Habitat. Other older or less precise geographic locations recorded within the U.C. Riverside database include: Santa Ana River, Prado Park, North Peak Conservation Bankand Temecula Creek, all of which are conserved within Criteria Area and Public/Quasi-Public Lands. Recent distribution information includes three locations within the Prado Basin/Santa Ana River area and Poorman Reservoir (Pike et al. 2001, Baumgartner 2001 pers. comm.)
There are definable locations for focusing conservation efforts where the species has been observed or has been documented to breed in the past. The five Core Areas include the following: (1) Prado Basin/Santa Ana River, including Chino Creek, Mill Creek, and the Santa Ana River both up- and downstream of the Prado Dam (9,670 acres); (2) Temescal Wash including Alberhill Creek (estimated as subunit 3 of Temescal Canyon Area Plan plus Proposed Constrained Linkage 6 and Proposed Linkage 2; 4,290 acres); (3) Murrieta Creek (Proposed Constrained Linkage 13; 1,400 acres); (4) Temecula Creek (Proposed Constrained Linkages 14 and 24; 830 acres); (5) San Timoteo Canyon (Proposed Linkages 5, 12 and Proposed Linkage 22; 2,140 acres). Each Core Area will include at least 100 meters of undeveloped landscape adjacent to the riparian woodland and scrub Habitat and contain unfragmented Habitat and landscape linkages to other Core Areas. The Core Areas must support a population of 20 pairs of cuckoos combined total. A total of 18,330 acres of Core Areas are conserved by the MSHCP as Criteria Area or Public/Quasi-Public designations within large blocks of a variety of Habitats. Within the Core Area at the Prado Basin/Santa Ana River, there are 5,010 acres of suitable Habitat for the western yellow-billed cuckoo with the MSHCP Conservation Area. All of the observations of the western yellow-billed cuckoo within the Prado Basin area are included within the Criteria Area or Public/Quasi-Public Lands. In addition, there are several single locations that have been identified as recent occurrences of the western yellow-billed cuckoo. These include Poorman Reservoir and North Peak Conservation Bank, both of which are located within Criteria Area or Public/Quasi-Public designations.
Species specific conservation measures for the western yellow-billed cuckoo include maintenance of the hydrological processes of the riparian drainages where the cuckoo occurs and the restoration of Habitat wherever appropriate. These hydrological processes and the supplemental rehabilitation or restoration of native riparian vegetations provide the necessary conditions for the growth and development of broad, luxuriant riparian Habitats as well as the humid microclimate conditions that are essential for the western yellow-billed cuckoo. Nesting western yellow-billed cuckoo generally prefer areas of extensive riparian Habitat with high humidity and moving water courses. There are limited locations within the Plan Area where water is available and Habitat is extensive enough to meet these species specific requirements. Ultimately, a water table close enough to the surface to support riparian vegetation is necessary. Maintaining and increasing the riparian Habitats within the potential and currently documented locations of the western yellow-billed cuckoo by preserving the hydrological processes within the drainages that supports the potential Habitat is an important conservation measure. Areas to which this conservation measure applies (in addition to all areas recently documented as recently occupied) include the Temescal Wash including Alberhill Creek, Wasson Canyon, Murrieta Creek, Temecula Creek, Vail Lake, Wilson Valley, Bautista Creek, Tucalota Creek, Lake Skinner, Potrero Creek, and San Timoteo Canyon. Due to past land practices, some of these drainages (or parts thereof) may not be currently considered suitable for the western yellow-billed cuckoo for nesting, however, due to lack of information on the dispersal requirements, these riparian drainages may be used by the species for localized or migratory movements. Activities that will be avoided within western yellow-billed cuckoo occupied areas include new water developments and flood control projects which may reduce and modify the Habitat for the species. Within the MSHCP Conservation Area, hydrology may be maintained by preventing diversion and channelization of natural watercourses which results in diminished surface flows and increased salinity of residual flows. Channelization alters streambanks and fluvial dynamics necessary to maintain the native riparian vegetation.
Implementation of Objective 3 will maintain or, if feasible, improve the riparian Habitats within the recent documented locations of the western yellow-billed cuckoo at the Prado Basin, Santa Ana River, North Peak Conservation Bank and Poorman Reservoir. Additionally, implementation of Objective 3 will maintain or improve the potential yellow-billed cuckoo Habitat (including potential core and other areas) and potential Habitat linkages within the riparian areas along the Santa Ana River both upstream and downstream from Prado Dam, Temescal Wash including Alberhill Creek, Wasson Canyon, Murrieta Creek, Temecula Creek, Vail Lake, Wilson Valley, Bautista Creek, Tucalota Creek, Lake Skinner, Potrero Creek, and San Timoteo Canyon. The maintenance or improvement of Habitat at all locales will be accomplished by preserving the hydrological processes within the drainages that support the potential Habitat and by selectively restoring, rehabilitating or revegetating all such areas that are currently fragmented or otherwise degraded by, for instance, infestations of exotic plants and animals. Each MSHCP Conservation Area manager responsible for a Core Area identified above will evaluate the condition of the riparian vegetation within the Core Area and maintain a program to enhance, restore, and/or create riparian Habitat within the Core Area. The Protection of Species Associated with Riparian/Riverine Areas and Vernal Pools and Adjacency Policies will be implemented, including for waterways that flow into or out of the MSHCP Conservation Area.
Objective 4 provides the conservation of additional areas within the Criteria Area that are identified as important to the western yellow-billed cuckoo. This Objective will be met through implementation of the Protection of Species Associated with Riparian/Riverine Areas and Vernal Pools Policy presented in Section 6.1.2 of the MSHCP, Volume I. Wetland mapping assembled as part of that policy will be reviewed as part of the project review process and if suitable western yellow-billed cuckoo Habitat, defined as cottonwood or willow riparian Habitat adjacent to flowing water or saturated soils, is identified on the wetland maps, a focused survey for western yellow-billed cuckoo will be conducted by a qualified biologist in accordance with accepted protocol. If survey results are positive, 100 percent of the occupied portions of the property that provide for long-term conservation value for the cuckoo will be conserved in a manner consistent with conservation of the cuckoo. This will involve including 100 meters of undeveloped landscape adjacent to the Habitat conserved. The MSHCP Plan also will maintain (once every 3 years) the continued use of, and successful reproduction at 75 percent of the known western yellow-billed cuckoo occupied Core Areas (including any nesting locations identified in the MSHCP Conservation Area in the future). Successful reproduction is defined as a nest which fledged at least one known young.
MSHCP Conservation Area Configuration Issues
Several large blocks of Habitat supporting or potentially supporting the western yellow-billed cuckoo will be conserved as Criteria Area and Public/Quasi–Public Lands, including the Prado Basin and Santa Ana River, Temescal Wash, Murrieta Creek, Temecula Creek, and San Timoteo Creek. Additional large blocks of Habitat that will be be conserved include Lake Skinner, Vail Lake/Wilson Valley, Potrero Creek, and Bautista Creek. Most of these large blocks of Habitat have not been mapped as containing western yellow-billed cuckoos. However, these Habitat blocks may expand in riparian Habitat in the future and may contain the permanent water source that is required by the species. These patches may provide suitable Habitat for the species in the future. The only area currently occupied for breeding apparently is the Prado Basin/Santa Ana River area. Two other locations, both of which are conserved in the MSHCP Conservation Area include Poorman Reservoir and North Peak Conservation Bank. The configuration of the MSHCP Conservation Area also provides linkages of Habitat for the species. The Prado Basin Core Area is linked along the Santa Ana River to San Bernardino and Orange counties. This riparian area is tenuously linked to the south by the Temescal Wash to Lake Mathews and Lake Elsinore. Riparian Habitat within the Vail Lake area is linked to the Lake Skinner-Diamond Valley Lake area via Tucalota Creek. The Vail Lake area is also linked to the Santa Rosa Plateau and then to the Santa Margarita River by the riparian Habitat in Temecula Creek and Murrieta Creek. The Badlands area provides a major Habitat block that provides a linkage to Potrero Creek and Lake Perris and San Jacinto Wildlife Area.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 8,970 acres of suitable Conserved Habitat and at least 5 Core Areas and the additional current known locations within large blocks of Habitat in the MSHCP Conservation Area. The MSHCP Conservation Area will maintain (once every 3 years) the continued use of, and successful reproduction at 75 percent of the known western yellow-billed cuckoo occupied Core Areas (including any nesting locations identified in the MSHCP Conservation Area in the future). Implementation of Objective 4 will provide the conservation of additional areas within the Criteria Area that are identified as important to the western yellow-billed cuckoo through wetland mapping assembled as part of the Riparian/Riverine Areas and Vernal Pools Policy (Section 6.1.2, Volume 1). This objective provides for conservation of 100 percent of the occupied portions of the property that provide for long-term conservation value for the western yellow-billed cuckoo. In addition, implementation of Objective 3 for this species will maintain or, if feasible, improve the riparian Habitats within the recent documented locations and potential Habitat and potential Habitat linkages within riparian areas by preserving the hydrological processes within the drainages that support the potential Habitat and, if feasible, by selectively restoring, rehabilitating or revegetating all such areas that are currently fragmented or otherwise degraded.
The MSHCP has been designed to preserve the areas with the known Core Areas of the species, including the Prado Basin/Santa Ana River. The Prado Basin is an important Core Area for the western yellow-billed cuckoo. Additionally, some of the smaller recently occupied riparian Habitat patches, and the larger riparian Habitat blocks that apparently have not been recently occupied, may provide management and restoration opportunities that are no longer available within portions of the core population areas. The Conservation Strategy for this species includes: (1) pre-construction surveys of potential Habitat areas that cannot be avoided, (2) assessments of the current and future utility of Habitat areas, and (3) the means to secure or otherwise conserve additional Habitat areas to expand the MSHCP Conservation Area until the continuing preservation of the yellow-billed cuckoo and its Habitat results in the conservation of the species that is currently on the verge of extirpation within the Plan Area and a large majority of California as a whole.
INCIDENTAL TAKE
Approximately 2,580 acres (about 22 percent) of suitable yellow-billed cuckoo Habitat will be outside the Criteria Area and Public/Quasi Public Lands and individuals within these areas may be subject to Incidental Take. None of the Core Areas for this species are outside the Criteria Area and Public/Quasi Public Lands. Additionally, implementation of the Riparian/Riverine Areas and Vernal Pools and adjacency policies, maintenance and improvement of Habitat, and protection and management of 100 percent of the area with conservation value of any site where the species is found will minimize Take of the species.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The UCR location database contain 9 records for the western yellow-billed cuckoo dating from 1888 to 1990. Two of these records are dated after 1990 and are of high precision. One of these locations is within the Prado Basin/Santa Ana River area and one is in the North Peak Conservation Bank. The USFWS has documented the presence of the species in the past for the Prado Basin as discussed below. Additionally, there is one anecdotal observation within Poorman Reservoir that is not within the UCR database. Due to its Habitat requirements, there are not likely to be many additional records of the species. Breeding has not been confirmed although the birds have been noted to be paired and defending territories.
The literature is relatively limited for this species in spite of the fact that it is a state listed species. There are many aspects of the life history that are unknown including territorial spacing, site tenacity and fidelity, demographic information, and population regulation.
Habitat and Habitat Associations
Yellow-billed cuckoos as a whole may nest in a variety of Habitats including open woodland, parks, and riparian woodland (AOU 1998). By contrast, the western yellow-billed cuckoo in California requires dense, wide riparian woodlands with well-developed understories for breeding (Garrett and Dunn 1981). It occurs in densely foliaged, deciduous trees and shrubs, especially willows which are required for roost and nest sites. It is restricted when breeding to river bottoms and other mesic Habitats where humidity is high and where the dense understory abuts slow-moving watercourses, backwaters or seeps (Zeiner, et al. 1990). Willow is almost always a dominant component of the vegetation. Within the Sacramento Valley, it also utilizes adjacent orchards, especially walnut. Along the Colorado River, it may inhabit mesquite thickets where willow is absent (USFWS 2001).
Biogeography
The yellow-billed cuckoo species, as a whole, summer and nest from interior California east to New Brunswick sporadically southward to southern Mexico. The species presumably migrates throughout much of North America and winters primarily from northern to central South America (AOU 1998).
The northern limit of breeding of the western yellow-billed cuckoo in the coastal states is now in Sacramento Valley, California and the northern limit of breeding in the western interior states is southern Idaho (USFWS 2001). Zeiner, et al. (1990) summarize the distribution, abundance, and seasonality of the western yellow-billed cuckoo within California as follows. It is an uncommon to rare summer resident of valley foothill and desert riparian Habitats in scattered locations in California. Along the Colorado River, the breeding population on the California side is estimated at 180 pairs (Gaines 1977). Perhaps 100, or fewer, additional pairs reside in the Sacramento and Owens valleys; along the South Fork of the Kern River, Kern County; along the Santa Ana River, Riverside County; and along the Amargosa River, Inyo and San Bernardino counties. Also it may nest along the San Luis Rey River, San Diego County. It usually arrives from South American wintering areas in June, and departs by late August or early September.
It was formerly much more common and widespread throughout lowland California, but the numbers are drastically reduced by Habitat loss (Grinnell and Miller 1944, Gaines 1974, Garrett and Dunn 1981). The historic breeding range in California extended northwest from San Diego County along the coast through San Francisco Bay to Sonoma County, San Joaquin and Sacramento valleys, from Kern County to Shasta County. and many outlying sites in Siskiyou, Inyo, and San Bernardino Counties (Hanna 1937; Hughes 1999).
Known Populations Within Western Riverside County
Up to seven cuckoo territories, three pairs during the 2001 breeding season, have been documented in the western Riverside County area in recent years; all of these were located in the Prado Basin or adjacent, Riverside County reach of the Santa Ana River (USFWS 1999 unpublished data; Pike 2001 pers. comm.). The three locations detected in 2001 include a location near Mill Creek, a location north along Chino Creek, and a male observed with a female on the El Prado Golf Course (Pike et al. 2001). None of these locations was confirmed to be a breeding location (Pike et al. 2001). The Prado Basin birds may represent the only summering location in southern California away from the Colorado River. Breeding of yellow-billed cuckoos has been confirmed only once in the Prado Basin during 14 years of observations there (USFWS 1999 unpublished data).
Geographic locations recorded within the U.C. Riverside database include: Santa Ana River, Prado Park, North Peak Conservation Bank, Poorman Reservoir, and Temecula Creek. These last three records are either old, low precision records, or were not confirmed for breeding activity (Baumgartner 2001 pers. comm.).
Biology
Genetics: Two subspecies of the western yellow-billed cuckoo have been recognized although the validity of these has been debated. The western subspecies, C. a. occidentalis is considered to be grayer, larger, with a proportionately larger and stouter bill. Statistical studies of the species have led to contradictory conclusions and the results appear equivocal, however recent cytochrome b gene sequence studies indicate the haplotypes of the eastern and western subspecies differ by four fixed base changes suggesting they diverged 205,000 to 465,000 years ago. Based on these genetic studies and the fact that the timing of migration and breeding appears to be different in the two subspecies, it has been recommended that the 2 subspecies be retained (USFWS 2001; Pruett et al.. 2001; Hughes 1999).
Diet and Foraging: The western yellow-billed cuckoo feeds mainly on large insects including cicadas, katydids, and caterpillars (Hamilton and Hamilton 1965). The yellow-billed cuckoo is primarily a foliage gleaner, although they may sally from a perch and catch flying prey or drop to the ground to catch grasshoppers or tree frogs (Laymon 1998). In an area in the Central Valley it forages predominantly in riparian vegetation (55 percent), one third of the time in white alder, and 12 percent of the time in orchards. During the breeding season, the foraging areas of nesting pairs may overlap. The mean size of foraging areas is 19.6 hectares of which 10 hectares is usable Habitat for foraging (Hughes 1999).
Daily Activity: The western yellow-billed cuckoo exhibits year-long, diurnal activity (Zeiner et al. 1990).
Reproduction: Breeding of the western yellow-billed cuckoo occurs in dense, wide riparian woodlands with well-developed understories. It nests typically in sites with at least some willow, dense low-level or understory foliage, and wooded foraging spaces in excess of 93 meters (300 feet) in width and 10 hectares (25 acres) in area (Gaines 1974, 1977). It is restricted when breeding to river bottoms and other mesic Habitats where humidity is high and where the dense understory abuts slow-moving watercourses, backwaters or seeps (Zeiner, et al. 1990). In arid regions individuals are restricted to river bottoms, ponds, swampy areas and damp thickets with nesting occurring in willow, cottonwood and mesquite (Hughes 1999). The species appears to be restricted to breeding in large blocks of riparian Habitats, particularly woodlands with cottonwoods and willows. The dense understory foliage appears to be an important factor in the nest site selection, while the cottonwood trees are an important foraging Habitat (Laymon et al. 1997). Nesting of the yellow-billed cuckoo occurs almost exclusively close to water and biologists have hypothesized that the species may be restricted to nesting in moist river bottoms in the west because of humidity requirements for successful hatching and rearing of the young. Nesting peaks later than in most other riparian species (mid-June through August) and may be triggered by an abundance of the cicadas, katydids, caterpillars, or other large prey which form the bulk of the diet (USFWS 2001).
The nest is a flimsy, open cup of twigs built on a horizontal limb of a tree or shrub at the height of 0.6 to 7.8 meters (2-25 feet). The western yellow-billed cuckoo shows a preference for nesting on east facing branches and have a very strong preference for placing the nest in a willow tree within the riparian Habitat (Amundson et al. 2000). The clutch size is variable but usually it is two or three and development of the young is very rapid (USFWS 2001). Incubation is begun immediately so the eggs hatch asychronously thus allowing brood reduction if food resources are limiting (Laymon 1998). In California, most eggs are laid in mid-June to mid-July. The species is monogamous. Incubation lasts 11-12 days with a breeding cycle of 17 days from egg-laying to fledging of young (Preble 1957; USFWS 2001; Laymon 1998). Western populations are thought to be single-brooded (Hughes 1999). Both parents incubate eggs and occasionally non-parents tend nests as well (Hughes 1999). Both sexes care for the altricial young. The young may leave the nest at 6-9 days in a helpless condition (Bent 1940, Hamilton and Hamilton 1965, Preble 1957). The chick leaves the nest at a very undeveloped condition and runs along a supporting limb to meet the adult approaching with food. It then disappears into the foliage above the nest where the adult attends (Hughes 1999).
Survival: Populations of cuckoos may be limited by food availability given that the youngest chick is not fed or pushed from nest when food availability is limited (Hughes 1999). Annual reproductive success is highly variable. Four nests in California all fledged young, however, only 64 percent of the eggs hatched, 57 percent of the eggs fledged young, and 43 percent of the offspring survived more than one week. The mean number of surviving young per nest is 1.5 (Hughes 1999). The number of young hatched at the South Fork Kern River averages 2.53 young/nest with the number of young fledged averaging 2.14 young/nest (Laymon 1998). Western yellow-billed cuckoos are capable of double and even triple brooding under good conditions so the average number of young can be much higher, however double and triple brooding is very rare (Laymon 1998).
Dispersal: The young yellow-billed cuckoos leave the nest at about seven to nine days (Hughes 1999). The young are tended by their parents for at least two weeks after fledging (Laymon 1998). The species is a long distance migrant, migrating predominantly at night (Hughes 1999).
Socio-Spatial Behavior: The western yellow-billed cuckoo appears to require large blocks of riparian Habitat for nesting. They are loosely territorial in that they do not defend a territory but given uniform Habitat they are regularly spaced through the landscape (Laymon 1998). Along the Sacramento River, they occupied home ranges which vary from 3 to 40 hectares (20 to 100 acres) or more of riparian Habitat (Gaines 1974; Laymon et al. 1993; Laymon and Halterman 1989). Home ranges in the south fork of the Kern River averaged about 17 hectares. Nesting densities ranging from 1 to 15 pairs per 40 hectares in a New Mexico population (USFWS 2001).
Community Relationships: The western yellow-billed cuckoo uses a distraction display to draw potential predators away from the nest (Laymon 1998). Red-shouldered hawks and northern harriers have been observed preying on nestlings. On the Sacramento river there appears to be an inverse relationship between the presence of cuckoos and scrub jays, indicating a possible aversion by the cuckoos to nesting at sites with scrub jays (Laymon 1998).
Threats to Species
Western yellow-billed cuckoos formerly nested nearly throughout the lowlands of southern California and were, at one time, fairly common to common in some areas (Grinnell and Miller 1944). Numbers in California and other western areas have declined markedly in recent decades with destruction of riparian Habitats (Laymon and Halterman 1987). The principal causes of riparian Habitat losses are conversion to agriculture and other uses, dams and river flow management, stream channelization and stabilization, and livestock grazing. Available breeding Habitats for the western yellow-billed cuckoo have also been substantially reduced in area and quality by groundwater pumping and the replacement of native riparian Habitats by invasive non-native plants including tamarisk and giant cane. A detailed analysis of the effects of tamarisk was prepared for the 12-month Finding for a Petition to List by the USFWS (2001). Tamarisk is not as great of an exotic pest in the Plan Area as it is in other areas. Of greater concern is the exotic plant giant cane which does occur within the Plan Area in large quantities. This plant species may cause similar degradation to riparian Habitat as tamarisk resulting in low species diversity and low structure diversity.
Fragmentation of riparian Habitat also reduces the quality of the riparian Habitat for the western yellow-billed cuckoo. Fragmentation results in the loss of patches large enough to sustain local populations, leading to local extinctions and the potential loss of migratory corridors which may affect the ability of the species to recolonize the Habitat patches (USFWS 2001). Habitat fragmentation in California has been shown to exclude individuals where patch size is less than 100 x 300 meters (Hughes 1999).
Overuse of riparian Habitat by livestock has been a factor in the degradation and modification of riparian Habitats in the western United states. The effects include changes in plant community structure and species composition as well as the relative abundance of species and plant density. These changes are often linked to more widespread changes in watershed hydrology and in some drainages may cause water flows to become sub-surface for some length of the stream (Ortega 2001 pers. comm.).
Although the major continuing threat to western yellow-billed cuckoos in southern California is almost certainly Habitat destruction (Garrett and Dunn 1981), there may be other as yet unidentified threats or impacts that are operative on the breeding grounds, wintering grounds, or both. Pesticides may affect behavior or cause death (Hughes 1999). In areas where riparian Habitat borders agricultural lands, pesticide use may affect western yellow-billed cuckoos indirectly by reducing prey numbers or directly by poisoning nestlings if sprayed in areas where the birds are nesting (USFWS 2001).
Special Biological Considerations
Agriculture, urbanization, and low water tables have reduced the available Habitat for the western yellow-billed cuckoo. This Habitat loss was notable as early as 1911. Important Habitat features that appear to be required by the cuckoo include dense willows, proximity to water, extensive river bottom vegetation, and at least 10 hectares per pair (Gaines 1974). The species occurs where riparian vegetation exceeds 300 meters in length and 100 meters in width, water is present within 100 meters and there is a dense understory (Gaines 1974).
Two Habitat models for the western yellow-billed cuckoo have concluded that willow-cottonwood Habitat of any age with high humidity and a Habitat breadth of 100 meters (325 feet) was necessary for suitable western yellow-billed cuckoo Habitat (Laymon 1998). Additional research based on occupancy rates allowed for the refinement of these requirements and Laymon and Halterman (1989) concluded that sites greater than 80 hectares (200 acres) in extent and wider than 600 meters (1950 feet) were optimal, that sites 41 to 80 hectares (101-200 acres) in extent and wider than 200 meters (650 feet) were suitable, sites 20 to 40 hectares (50 to 100 acres) in extent and 100 to 200 (325 to 650 feet) in width were marginal and sites less than 15 hectares (38 acres) in extent and less than 100 meters (325 feet) in width were unsuitable. Laymon (1998) also cited studies that found that Habitat patch area, the extent of Habitat in a 8 kilometer (5 mile) section of river and presence of low woody vegetation were the most important variables in explaining the distribution of cuckoos. Laymon (1998) also reported a study that indicated that micro-Habitat requirements are also important and that nesting groves at the South Fork Kern River are characterized by higher canopy closure, higher foliage volume, intermediated basal area, and intermediate tree height when compared to random sites.
The species has not noticeably increased within the Prado Basin during the course of 14 years of cowbird management and Habitat conservation efforts there (USFWS, 1999 unpublished data). By contrast, the local population of the endangered least Bell's vireo (Vireo bellii pusillus) has increased during that same time frame from 19 pairs to 270. Hughes (1999) reports that there may be fewer than 30 breeding pairs of the western yellow-billed cuckoo in California.
Hughes (1999) identifies restoration of riparian Habitats and elimination of pesticide spraying in orchards adjacent to riparian areas as key management measures. One study proposes that reestablishment of 23 subpopulations of 25 pairs each in the Sacramento Valley would require restoration of 10,380 hectares of riparian Habitat (Hughes 1999). Restoration of riparian Habitats have been shown to succeed also in establishment of breeding pairs in southern California (Hughes 1999).
LITERATURE CITED
Amundson, R. G., J. L. Atwood, A. J. Belsky, C. T. Collins, D. Dobkin, A. Harper, S. Hejo, J. M. Hughes, W. D. Koenig, S. A. Laymon, G. Monson, R. Noss, R. Ohmart, K. O'Keefe, F. A. Pitelka, P. G. Raven, S. Rohwer, S. Smallwood, T. B. Smith, P. Stacey, J. Terborgh, and P. L. Williams. 2000. Status of the Yellow-Billed Cuckoo. Letter to the Field Supervisor, U.S. Fish and Wildlife Service.
AOU (American Ornithologists' Union). 1998. Check-List of North American Birds. Seventh Edition. American Ornithologists' Union, Washington, D.C. 829 pp.
Baumgartner, M. 2001. Pers. comm.
Bent, A. C. 1940. Life histories of North American cuckoos, goatsuckers, hummingbirds and their allies. U.S. Nat. Mus. Bull. 176.
Gaines, D. 1974. Review of the status of the yellow-billed cuckoo in California: Sacramento Valley populations. Condor 76: 204-209.
Gaines, D. 1977. Current status and Habitat requirements of the yellow-billed cuckoo in California. Calif. Dept. Fish and Game, Sacramento. 94pp.
Garrett, K. and J. Dunn. 1981. Birds of Southern California: Status and Distribution. Los Angeles Audubon Society. 407 pp.
Grinnell, J. and A.H. Miller. 1944. The Distribution of the Birds of California. Pacific Coast Avifauna Number 27. Copper Ornithological Club, Berkeley, California. Reprinted by Artemisia Press, Lee Vining, California; April, 1986. 617 pp.
Hamilton, W. J., III, and M. E. Hamilton. 1965. Breeding characteristics of yellow-billed cuckoos in Arizona. Proc. Calif. Acad. Sci. Fourth Ser. 32: 405-432.
Hanna, W. C. 1937. California cuckoo in the San Bernardino Valley, California. Condor 39:57-59.
Hughes, Janice M. 1999. Yellow-billed cuckoo (Coccyzus americanus). In The Birds of North America, No. 418 (A. Poole and F. Gill eds.) The Academy of Natural Sciences, Philadelphia, PA and The American Ornithologists' Union, Washington, D.C.
Laymon, S. A. 1998. Partners in Flight Bird conservation Plan. Species: Yellow-billed Cuckoo. Http://www.prbo.org/calpif/htmldocs/species/riparian/ybcuacct.html.
Laymon, S. A. And M. D. Halterman. 1987. Can the western subspecies of yellow-billed cuckoo be saved from extinction? West. Birds 18: 19-25.
Laymon, S. A. and M. D. Halterman. 1989. A proposed Habitat management plan for yellow-billed cuckoos in California. USDA Forest Service Gen. Tech. Rep. PSW-110 p 272-277.
Laymon, S.A., P.L. Williams, and M.D. Halterman. 1993. Breeding status of the Yellow-billed Cuckoo in the South Fork Kern River Valley, Kern County, California: Summary report 1985-1996. Admin. Rep. USDA Forest service, Sequoia National Forest, Cannell Meadow Ranger District, Challenge Cost-Share Grant #92-5-13.
Nolan, V., Jr., and C. F. Thompson. 1975. The occurrence and significance of anomalous reproductive activities in two North American nonparasitic cuckoos Coccyzus spp. Ibis 117: 496-503.
Ortega, B. 2001. Dudek & Associates. Pers. comm.
Pike, J. 2001. USFWS. Pers. comm.
Pike, J., D. Pellegrini, L. Hays, and R. Zembal. 2001. Least Bell's vireos and southwestern willow flycatchers in Prado Basin of the Santa Ana River watershed, CA. Prepared for the Orange County Water District and U.S. Fish and Wildlife Service. 21 pp.
Preble, N. A. 1957. Nesting habits of the yellow-billed cuckoo. Am. Midl. Nat. 57: 474-482.
Pruett, C. L., D. D. Gibson, and K. Winker. 2001. Molecular "cuckoo clock" suggests listing of the western yellow-billed cuckoos may be warranted. Wilson Bulletin 113: 228-231.
USFWS. 1999. Unpublished data.
United States Fish and Wildlife Service (USFWS). 2001. Endangered and Threatened Wildlife and Plants; 12-month finding for a petition to list the yellow-billed cuckoo (Coccyzus americanus) in the Western Continental United States. Federal Register 50 CRF Part 17; Vol 66, No. 143: 38611-38626.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
white-faced ibis (Plegadis chihi)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
white-faced ibis (Plegadis chihi)
Status:
State: Species of Special Concern
Federal: Federal Special Concern species; Fish and Wildlife Service Region 1 Species of Management Concern
GROUP DESIGNATION AND RATIONALE
Group 2
The white-faced ibis is sparsely distributed throughout the Riverside Lowlands Bioregions of the MSHCP Plan Area within its suitable Habitat. It occurs at some of the areas of freshwater marsh Habitat but is only documented for breeding at two locations: Prado Basin and Mystic Lake/San Jacinto Wildlife Area. There appear to be several Core Areas in addition to the two breeding areas including a section of the Santa Ana River, Collier Marsh, and San Jacinto Valley. The breeding locations are few and there are not likely to be more that have not been discovered. These breeding locations require conservation. The species uses a wide variety of Habitats for foraging during winter and transient visits including agricultural land, grassland, and areas at the edges of drainages. It is very opportunistic and flexible for foraging requirements.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information existing at the time of MSHCP preparation. Pursuant to the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives may be adjusted as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 340 acres of suitable primary breeding Habitat including freshwater marsh Habitat within the Riverside Lowlands bioregion.
Objective 2
Include within the MSHCP Conservation Area at least the two known breeding locations and foraging areas at the Prado Basin/Santa Ana River (9,670 acres) and Mystic Lake/San Jacinto Wildlife Area (Subunit 4 of Reche Canyon/Badlands Area Plan; 2,690 acres), and the core foraging areas at Collier Marsh (Proposed Linkage 2; 160 acres) and San Jacinto Valley (Subunit 1 of Lakeview/Nuevo Area Plan; 3,650 acres).
Objective 3
Include within the MSHCP Conservation Area at least 57,620 acres of suitable secondary foraging Habitat including playas and vernal pools, agriculture (field crops), grassland, cismontane alkali marsh, and riparian scrub, woodland and forest within the Riverside lowlands Bioregion.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
The white-faced ibis is virtually restricted to emergent vegetation and islands along the margins of open water areas for nesting. However, the species may use a wide variety of Habitats, including flooded agriculture lands and grasslands in a very nomadic and unpredictable manner for foraging (Garrett and Dunn 1988). Because they will opportunistically use a relatively wide variety of wetlands for various parts of their life history, a wide range of Habitats has been included for this analysis as secondary Habitats. For the purpose of the conservation analysis, potential Habitat for the white-faced ibis includes freshwater marsh for the primary nesting Habitat (which also includes opportunities for foraging) and playas and vernal pools, cismontane alkali marsh, riparian scrub, woodland and forest (provides edge Habitat for foraging and buffer to protect the emergent vegetation), agriculture lands (field crops) and grasslands as secondary foraging Habitat. Their nesting Habitat, which is important to address separately, consists of freshwater marsh. Based on these Habitats, the Plan Area supports approximately 400 acres of primary nesting Habitat for the white-faced ibis. The Plan Area supports approximately 244,120 acres of secondary foraging Habitat for the white-faced ibis . Table 1 shows the conservation and loss of potential Habitat for the white-faced ibis. Overall, approximately 340 acres (85 percent) of potential primary nesting Habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public Lands. Additionally, approximately 57,620 acres (24 percent) of potential secondary foraging Habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public Lands.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
WHITE-FACED IBIS
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| Primary Habitat for Nesting Areas in Riverside Lowland Bioregion | |||||||
| Freshwater Marsh | 400 | 100 | 240 | 340 | 0 | 60 | 60 |
| Subtotal for Nesting Habitat | 400 | 100 (25%) |
240 (60%) |
340 (85%) |
0 (0%) |
60 (15%) |
60 (15%) |
| Secondary Habitat for Foraging in Riverside Lowland Bioregion | |||||||
| Playas and Vernal Pools | 7,870 | 3,820 | 2,890 | 6,710 | 0 | 1,160 | 1,160 |
| Agriculture (field croplands) | 115,650 | 5,590 | 9,820 | 15,410 | 490 | 99,750 | 100,240 |
| Grassland | 109,960 | 12,820 | 14,650 | 27,470 | 5,650 | 76,840 | 82,490 |
| Cismontane Alkali Marsh | 10 | 10 | 0 | 10 | 0 | 0 | 0 |
| Riparian Scrub, Woodland, Forest | 10,630 | 2,420 | 5,600 | 8,020 | 150 | 2,460 | 2,610 |
| Subtotal for Foraging Habitat | 244,120 | 24,660 (10%) |
32,960 (14%) |
57,620 (24%) |
6,290 (3%) |
180,210 (74%) |
186,500 (76%) |
| TOTAL | 244,520 | 24,760 (10%) |
33,200 (14%) |
57,960 (24%) |
6,290 (3%) |
180,270 (74%) |
186,560 (76%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
In addition, the Riparian/Riverine Areas and Vernal Pools policy described in Section 6.1.2 provides for conservation of wetlands which provide Habitat for this species through avoidance and minimization. Mitigation for impacts to wetlands shall be incorporated in accordance with the "No Net Loss" policy of federal and state wetland regulations. The proposed mitigation shall be directly related to the functions and values of the wetland as related to this species and result in equivalent replacement. This policy is important in providing protection for the nesting Habitat and the Habitats that are used very frequently for foraging which include the emergent vegetation, mudflats and inundated areas.
As described above under Data Characterization, 17 of the 27 recent point localities have a high location precision of "1." Of these 17 point localities, 6 will be inside the Criteria Area or Public/Quasi-Public Lands. In addition, the one known nesting colony location and one historical or likely nesting location are within the Criteria Area or Public/Quasi-Public Lands. A total of 11 point localities will be outside of the MSHCP Conservation Area. However, these locations, if within a wetland area, will continue to receive protection by the wetland policy and otherwise the locations are likely a transient foraging observation that will be difficult to predict for occurrence in the future. Conservation of this species will be considered from a landscape perspective because the species is very flexible and opportunistic for its foraging requirements and occurs in relatively low number within the MSHCP Plan Area.
The key nesting location (Prado Basin) and historic or likely nesting location (Mystic Lake/San Jacinto Wildlife Area) that will be essential for conservation of the species will be conserved. Additionally, the Core Areas for foraging at the Santa Ana River, Collier Marsh, and San Jacinto Valley will also be conserved. Conserving large blocks of suitable Habitat within the area of known occurrences will likely capture additional localities of the white-faced ibis.
MSHCP Conservation Area Configuration Issues
Several large blocks of Habitat supporting the current known locations, nesting colony, and potential foraging and nesting locations of the white-faced ibis will be conserved as Criteria Area or Public/ Quasi-Public designations, including the Prado Basin, Santa Ana River, Mystic Lake/San Jacinto Wildlife Area with adjacent playa Habitat, Collier Marsh, and San Jacinto Valley. Other locations where they have been observed that will be conserved include Alberhill and Motte-Rimrock Reserve. Additional areas that provide foraging Habitat and potential nesting Habitat include Lake Skinner-Diamond Valley Lake, Lake Mathews, Wasson Canyon, Temecula and Murrieta creeks, San Timoteo Creek, Temescal Wash, and Vail Lake/Wilson Valley. As identified above, the species occurs within the MSHCP Plan Area predominantly as a transient or migrant and, as such, the MSHCP Conservation Area will provide adequate Habitat for foraging during nomadic visits to the area and migratory stopovers as well as the primary Habitat containing potential nest sites with adequate protection around each nest site and foraging areas during the breeding season. These MSHCP Conservation Area areas are linked as well, however the white-faced ibis, due to its ability to move long distances and its nomadic behavior, may rely less on the linkages than other species.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 340 acres of suitable Conserved Habitat composed of the nesting Habitat (freshwater marsh) and 57,620 acres of suitable Conserved Habitat composed of the foraging Habitat (playas and vernal pool, agriculture, grassland, cismontane alkali marsh, and riparian scrub, woodland, and forest). In addition, the two core breeding areas as well as the core foraging area at Collier Marsh, along the Santa Ana River, and within San Jacinto Valley are included in the MSHCP Conservation Area. The current population size of the white-faced ibis is unknown due to its nomadic and transient nature.
INCIDENTAL TAKE
About 60 acres (about 15 percent) of potential primary nesting Habitat for the white-faced ibis will be outside the Criteria Area and Public/Quasi-Public designations, and individuals within these areas will be subject to Incidental Take consistent with the Plan. About 186,500 acres of potential secondary foraging Habitat for the white-faced ibis will be outside the Criteria Area and Public/Quasi-Public designations, or about 76 percent of the total potential Habitat. Of this, there is no primary nesting Habitat within Rural/Mountainous designations and a limited amount of secondary foraging Habitat (6,290 acres or 3 percent). The Rural/Mountainous designation areas are not within areas used by the white-faced ibis. It should be noted that the Riparian/Riverine Areas and Vernal Pools policy presented in Section 6.1.2 of the MSHCP, Volume I, will apply to wetland Habitat areas outside the MSHCP Conservation Area.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The UCR location database includes approximately 29 records for the white-faced ibis within the Plan Area dated from 1897 to 1999. Two of these records are museum records and are dated from 1897. The balance of the records, a total of 27, are relatively recent (within the past 10 years) and of these recent records, 17 are high precision records that can be accurately placed within the area. The Habitat types associated with these recent and high precision data records include grassland, open water, alkali playa, crop lands, riparian, feed yards, and residential, all likely Habitats for occurrence of the white-faced ibis. The residential Habitat records may reflect records that are either no longer extant or where the location is a small pocket of suitable Habitat within or adjacent to a developed area.
The literature available on the white-faced ibis is relatively low. It is focused on the natural history of the species, however, some of the details of its natural history have not been determined. A few general ornithological reference treatments, along with a relatively complete and recent natural history account, have been prepared for the species. Little information is available with respect to the Plan Area other than general distribution and occurrence information.
Habitat and Habitat Associations
Within its breeding range in inland areas, the white-faced ibis occurs in mainly shallow marshes with islands of emergent vegetation. They occasionally occur on spoil banks created by dredging. They occur locally in flooded shoals and mangrove swamps. In the coastal areas of the southern portion of the range, the white-faced ibis nests mostly in wetlands of outer coastal plains, freshwater marshes of common reed, bulltongue, saltmeadow cordgrass and torpedo panic- grass. Many colonies in the southern coastal areas are found in saltwater marshes (Ryder and Manry 1994).
In southern California, extensive marshes are required for nesting (Garrett and Dunn 1981). The species prefers shallow, grassy marshes and nests in dense, fresh emergent wetland (Zeiner, et al. 1990).
Migrant and wintering white-faced ibis may be found foraging in shallow lacustrine waters, muddy ground of wet meadows, marshes, ponds, lakes, rivers, flooded fields, and estuaries (Zeiner et al. 1990). Habitat use by wintering ibis in California appears to vary by region: in the Sacramento Valley, ibis are concentrated in agricultural fields and managed wetlands; in the San Joaquin Valley, ibis appear to use grassland/wetlands; in the Coachella Valley/Salton Sea/Imperial Valley, the vast majority of ibis occur in irrigated agricultural lands particularly alfalfa and wheat; on the coastal slope of central and southern California, wintering ibis use a variety of Habitats including marshy pasture lands, managed or natural freshwater marsh, pond edges, lake shores, and margins of brackish lagoons and estuaries (Shuford et al. 1996).
In summary, most ibis wintering in California forage in managed wetlands or agricultural fields and private lands provide the majority of foraging Habitat in all of the state's main wintering areas (Shuford et al. 1996).
Biogeography
White-faced ibis breed locally in North America from Oregon eastward to North Dakota and southward to the Mexican plateau. The largest breeding colonies usually are in Utah, Nevada, Oregon, and coastal Texas and Louisiana (Ryder and Manry 1994). There are also breeding and wintering populations in South America and Mexico, as far south as central Chile and central Argentina, however, the details of the more southern distribution are less well known (AOU 1998). The species winters from California (locally) eastward to Texas and coastal Louisiana and southward to Guatemala (Ryder and Manry 1994).
Zeiner, et al. (1990) summarize the distribution, abundance, and seasonality of the white-faced ibis in California as follows. The white-faced ibis is an uncommon summer resident in sections of southern California, a rare visitor in the Central Valley, and is more widespread in migration. The white-faced ibis is a distant and local migrant; it is nonmigratory in some locations. It is absent from the northeastern plateau October to March. It winters mainly in the San Joaquin Valley and Imperial Valley, but is recorded widely as a transient. The population at the Salton Sea is reduced sharply from October to March, suggesting a southward migration. A few pairs bred in 1977 and 1978 at the Salton Sea, and in 1979 at Buena Vista Lagoon, San Diego County (Garrett and Dunn 1981). It has nested recently at Honey Lake, in the Klamath Basin, and at a few isolated areas in Central Valley (Airola 1980, McCaskie, et al. 1979, Ryder 1967). At the Salton Sea area, it is fairly common April to September, and uncommon through the winter. It is an uncommon transient elsewhere in southern California, and a very local winter visitor along the coast (Garrett and Dunn 1981). It is rare in the San Joaquin Valley, occurring mainly near Los Banos, August to April; and is rare on the northeastern plateau April to September (McCaskie, et al. 1979). Within southern California, the species is most often recorded during migration and winter, with nesting occurring only rarely in the coastal plain (Garrett and Dunn 1981).
In the 1960s and 1970s, nesting populations and numbers of colonies of the white-faced ibis decreased because of pesticide contamination and loss of Habitat to drought and drainage. In the 1980s and 1990s, the species increased as Habitat improved reclaiming the historic breeding range and expanding north to the northern portions of the United States (Ryder and Manry 1994). Formerly more common, especially in the San Joaquin Valley, the white-faced ibis no longer breeds regularly anywhere in California (Remsen 1978).
Known Population Within Western Riverside County
Although white-faced ibis have been repeatedly recorded in the Mystic Lake/San Jacinto Wildlife Area and previously bred there (Garrett and Dunn 1981), there currently is only one confirmed breeding colony in western Riverside County within the Prado Basin (L.R. Hays, USFWS, pers. obs.; Michael Patten, Riverside County Editor for American Field Notes and Past Secretary, California Bird Records Committee, pers. comm., 1998). Approximately 50 pairs have bred at that location in recent years. White-faced ibis have been recorded wintering in Prado Basin, Corona duck clubs, and San Jacinto Valley (Shuford et al. 1996). Migrants or wintering birds currently have be found in appropriate Habitat nearly throughout the Plan Area. Additional locations of the white-faced ibis have been documented for the Santa Ana River, Eastvale, Alberhill, Collier Marsh, Lake Riverside, San Jacinto Valley area, Moreno Valley, and Motte-Rimrock Reserve.
Biology
Genetics: The white-faced ibis is considered to be a subspecies of the glossy ibis by some ornithologists (Amadon and Woolfenden 1952).
Diet and Foraging: The diet of the white-faced ibis is mainly composed of aquatic and moist-soil insects, crustaceans and earthworms amphibians, small fishes, and miscellaneous invertebrates (Ryder and Manry 1994). It probes deep in the mud with its long bill, and also feeds in shallow water or on the water surface (Cogswell 1977). Ibises feed in large flocks of over 1,000 individuals (Ryder and Manry 1994). Individuals find prey either on the surface of the water or soil, or beneath the soil through probing (Ryder and Manry 1994).
The foraging Habitat of the white-face ibis includes shallowly flooded pond margins, reservoirs, and marshes (Ryder and Manry 1994). A 1988 study in the Great Basin Valley showed white-faced ibis to have a preference for alfalfa fields and less preference for corn, wheat-barley, pastures and oat fields (Bray, et al. 1988). Other preferences included fields which were located closer to the colony, larger fields, fields with clay and clay-loam soils and those which are irrigated. Irrigation fields were shown to be a valuable feeding Habitat for the species in this area.
Daily Activity: The white-faced ibis exhibits year-long, diurnal activity (Zeiner et al. 1990).
Reproduction: The white-faced ibis nests in dense, fresh emergent wetland (Zeiner, et al. 1990). The nest, which is made of dead tules or cattails, is built within tall marsh plants, sometimes on mounds of vegetation. According to Cogswell (1977), it rarely nests in trees, but it is not clear whether tree nesting has been recorded in California. Grinnell and Miller (1944), Palmer (1962), and Harrison (1978) did not mention tree nesting by this species. The nest components are generally made-up of the dominant vegetation in the nesting area and varies between populations (Ryder and Manry 1994).
The white-faced ibis is presumed to be monogamous (Ryder and Manry 1994). Pairs will re-nest, if initial nesting attempt fails (Ryder and Manry 1994). The earliest recorded breeding by a white-faced ibis was at two years of age (Ryder and Manry 1994).
The usual clutch size of the white-faced ibis is three to four eggs, but the clutch size may vary from two to five eggs (Ryder and Manry 1994). At Los Banos, eggs were present from May to July (Zeiner, et al. 1990). The eggs are incubated for 21 days, mostly by the female, and the young are fed in or near the nest for about five weeks (Cogswell 1977). Normally, pairs will have one brood per season (Ryder and Manry 1994). Nest success rates (percentage of nests producing one or more seven-day old chicks) were measured at 63 percent for populations in Utah (Ryder and Manry 1994). The number of seven- to ten-day old chicks per clutch average 1.42 to 2.99 (Ryder and Manry 1994). Individuals are apparently loyal to both breeding and roosting sites but will wander widely depending on water conditions and food availability (Ryder and Manry 1994).
Survival: Predation of eggs and nestling of the white-faced ibis occurs by gulls, magpies, night-herons, gallinules, owls, ravens as well as raccoons, skunks, coyotes and weasels (Ryder and Manry 1994). Botulism has been identified as a regular disease which kills white-faced ibises (Ryder and Manry 1994). Extremely high temperatures can be fatal to nestlings (Ryder and Manry 1994). Reproductive success is often effected by flooding which displaces nests. The oldest bird known in the wild is recorded at 14 year 6 months and for a bird in captivity at least 14 years (Ryder and Manry 1994).
Dispersal: Fledglings of the white-faced ibis first leave the nest at six to seven weeks of ages (Ryder and Manry 1994). The species undertakes regular north-south migrations (Ryder and Manry 1994).
Socio-Spatial Behavior: The average distance between nests of the white-faced ibis was 2 meters (7 feet) in nesting colonies studied by Burger and Miller (1977). Flocks foraging in wetlands tended toward shorter inter-individual distances when compared with flocks foraging in grasslands (Amat and Rilla 1994). The home range, during the nesting period, has been measured at 40-48 square kilometers in Idaho (Ryder and Manry 1994).
White-faced ibises are not generally aggressive and do not exhibit territorial behavior until the nesting season (Ryder and Manry 1994). Territories for nesting pairs comprise approximately one square meter around the nest (Ryder and Manry 1994).
Community Relationships: Food held by the white-faced ibis may be stolen by California gulls (Larus californicus) and grackles and ibises are sometimes attacked by American coots (Fulica americana) within coot territories (Ryder and Manry 1994).
Threats to Species
White-faced ibis historically were far more common at all seasons throughout California generally (Grinnell and Miller 1944) and southern California specifically (Garrett and Dunn 1981) The decline of the species has been attributed to the destruction of appropriate Habitat (Grinnell and Miller 1944). Destruction of marsh Habitat, especially along the southern coast and in the San Joaquin Valley, is perhaps the main factor responsible for the decline (Remsen 1978). Garrett and Dunn (1981) subsequently noted that measures should be taken to preserve the nesting Habitat of this species, which is declining throughout its range.
Humans entering active colonies of the white-faced ibis may cause partial or total desertion, particularly during the nest-site selection, nest-building, and incubation phases. Unattended eggs and small chicks are highly vulnerable to avian predators and to chilling or overheating (Ryder and Manry 1994).
Elsewhere in the range, pesticides have caused a decline in the numbers of the white-faced ibis (Terres 1980). The species is subject to eggshell thinning from DDT-DDE contaminants (Ryder and Manry 1994). Following severe drought, emergent wetland vegetation may take several years to recover to a condition suitable for white-faced ibis nesting (Ryder and Manry 1994).
Special Biological Considerations
The white-faced ibis breeding colony in the Prado Basin is one of very few that have recently existed in southern California as a whole. The area where the species breeds is carefully managed to minimize human disturbance and to maximize bulrush concentrations, which provide for the support and concealment of nests. Earnst, et al. (1988) suggest that the species will benefit from a landscape mosaic of well-distributed peripheral wetlands and persistent colony sites.
White-faced ibis has been identified by alfalfa growers as a pest because they trample the crops making it difficult to cut (Ryder and Manry 1994). Ibis have also allegedly caused harvest losses for crawfish farmers (Ryder and Manry 1994).
Earnst, et al. (1988) studied breeding colony dynamics of populations in the Great Basin and observed individuals to have the ability to move among colonies and rapidly colonize newly available wetlands when unfavorable conditions arise at current breeding locales.
In studying the species in southeastern Uruguay, Amat and Rilla (1994) found that flock size varied with Habitat and sex. Flocks foraging in wetlands tended toward larger flock sizes when compared with flocks foraging in grasslands (Amat and Rilla 1994). Females were proportionately more abundant in grasslands than in wetlands (Amat and Rilla 1994).
LITERATURE CITED
Airola, D. A., ed. 1980. California wildlife Habitat relationships program: Northeast Interior Zone. Vol III. Birds. U.S. Dep. Agric., For. Serv., Lassen Natl. For., Susanville. 590pp.
Amadon, D., and G. Woolfenden. 1952. Notes on the Matthews' collection of Australian birds. Am. Mus. Novit. No. 1564.
Amat, J.A. and F. D. Rilla. 1994. Foraging behavior of white-faced Ibises (Plegadis chihi) in relation to Habitat, group size, and sex. Colonial Water birds17: 42-49.
AOU (American Ornithologists' Union). 1998. Check-List of North American Birds. Seventh Edition. American Ornithologists' Union, Washington, D.C. 829 pp.
Bray, M. P. and D.A. Klebenow. 1988. Feeding ecology of white-faced ibis in a Great Basin Valley, USA. Colonial Water birds 11: 24-31.
Burger, J., and L. M. Miller. 1977. Colony and nest sites selection in white-faced and glossy ibises. Auk 94:664-676.
Cogswell, H.L. 1977. Water birds of California. Univ. California Press, Berkeley. 399 pp.
Earnst, Susan L., Larry Neel, Gary L. Ivey and Tara Zimmerman. 1988. Status of the White-faced Ibis: Breeding colony dynamics of the Great Basin population, 1985-1987, Colonial Waterbirds21: 301-313.
Garrett, K. and J. Dunn. 1981. Birds of Southern California: Status and Distribution. Los Angeles Audubon Society. 407 pp.
Grinnell, J. and A.H. Miller. 1944. The Distribution of the Birds of California. Pacific Coast Avifauna Number 27. Copper Ornithological Club, Berkeley, California. Reprinted by Artemisia Press, Lee Vining, California; April 1986. 617 pp.
Harrison, C. 1978. A field guide to the nests, eggs and nestlings of North American birds. W. Collins Sons and Co., Cleveland, OH. 416pp.
Hays, L. 1999. Pers.comm. U.S. Fish and Wildlife Service.
McCaskie, G., P. De Benedictis, R. Erickson, and J. Morlan. 1979. Birds of northern California, an annotated field list. 2nd ed. Golden Gate Audubon Soc., Berkeley. 84pp.
Palmer, R. S., ed. 1962. Handbook of North American birds. Vol. 1. Yale University Press, New Haven, CT. 567pp.
Patten, M. 1998. Pers.comm. Riverside County Editor for American Field Notes and Past Secretary, California Bird Records Committee.
Remsen, J. V. Jr. 1978. Bird Species of Special Concern in California. State of California. Department of Fish and Game. Supported by Federal Aid in Wildlife Restoration, Project Pr W-54-R-9, Nongame Wildlife Investigation, Wildlife Management Branch Administrative Report No. 78-1. 54 pp.
Ryder, R. A. 1967. Distribution, migration, and mortality of the white-faced ibis in North America. Bird-Banding 38:257-277.
Ryder, Ronald R. and David E. Manry. White-faced Ibis (Plegadis chihi). In The Birds of North America, No. 130 (A. Poole and F. Gill, Eds.) . Philadelphia: The Academy of Natural Sciences; Washington, D.C.: The American Ornithologists' Union.
Shuford, W. D., C. M. Hickey, R. J. Safran, and G. W. Page. 1996. A review of the status of the white-faced ibis in winter in California. Western Birds 27: 169-196.
Terres, J. K. 1980. The Audubon Society encyclopedia of North American birds. A. Knopf, New York. 1100pp.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
Williamson's sapsucker (Sphyrapicus thyroideus)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
Williamson's sapsucker (Sphyrapicus thyroideus)
Status:
State: None
Federal: None
GROUP DESIGNATION AND RATIONALE
Group 2
The species has declined rangewide, presumably from loss of large snags for nesting. Very little is known about its status, abundance, and distribution in the MSHCP Plan Area; there are only 5 known data points. Its conservation is largely dependent on activities within the San Bernardino National Forest and the Mt. San Jacinto State Park and private inholdings on these lands. Habitat for the Williamson's sapsucker includes montane coniferous forest dominated by lodgepole pines and firs, and oak woodlands and forests in the San Bernardino and San Jacinto mountains. Because the Habitat types that the Williamson's sapsucker uses for breeding and foraging are known but it requires specific micro-Habitat for nesting sites (snags), it has been placed as a Group 2 species.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 34,020 acres of suitable breeding, wintering, and dispersal Habitat for the Williamson's sapsucker including oak woodland and forest and montane coniferous forest within the San Bernardino Mountains and San Jacinto Mountains Bioregions.
Objective 2
Include within the MSHCP Conservation Area micro-Habitat (i.e., groups of large snags) in potential nesting Habitat.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
Breeding, wintering, and dispersal Habitat for the Williamson's sapsucker includes montane coniferous forest, and oak deciduous woodland and forest within the San Bernardino Mountains and San Jacinto Mountains Bioregions. Based on these Habitat types, the Plan Area supports approximately 46,290 acres of potential Habitat for the Williamson's sapsucker. Table 1 shows the conservation and loss of potential Habitat for the Williamson's sapsucker. Overall, approximately 34,020 acres (73 percent) of potential Habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public Lands.
This species occurs predominantly within the Forest Service lands within the San Bernardino and San Jacinto mountains Bioregions as a breeding and wintering species. It occurs predominantly within montane coniferous forest composed of lodgepole pines and firs as a breeding species and moves to lower elevation within these same Bioregions into the yellowpine forests and sometimes into oak woodland and forest. Within the breeding and wintering areas, conservation of this species is largely dependent on activities on Forest Service lands. Under the existing Forest Land allocation plan, these Habitats generally are located within the San Jacinto Wilderness area, San Jacinto Management area, and within some of the grazing allotments if appropriate Habitat is present, and also in the Mt. San Jacinto State Park. The Williamson's sapsucker has been documented to breed within the San Bernardino Mountains and the San Jacinto Mountains in the appropriate Habitat.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
WILLIAMSON'S SAPSUCKER
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| San Bernardino Mountains and San Jacinto Mountains Bioregions | |||||||
| Oak Woodlands and Forests | 16,490 | 300 | 13,320 | 13,620 | 850 | 2,020 | 2,870 |
| Montane Coniferous Forest | 29,800 | 20 | 20,380 | 20,400 | 40 | 9,360 | 9,400 |
| TOTAL | 46,290 | 320 (<1%) |
33,700 (73%) |
34,020 (73%) |
890 (2%) |
11,380 (25%) |
12,270 (27%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
As described below under Data Characterization, three relatively recent points have been documented for the MSHCP Plan Area. One point appears to be inside the MSHCP Conservation Area within Public/Quasi-Public lands of the San Bernardino National Forest. The two other recent point locations are within the Santa Ana River area and may reflect a nomadic movement. There are two additional older records (prior to 1990) inside the MSHCP Conservation Area within Public/Quasi-Public Lands of the San Bernardino National Forest. This species may also winter within higher elevation deciduous and coniferous (yellow pine) woodland and forest and may move nomadically during that time. Conservation of this species will be considered from a landscape perspective as well as a specific microHabitat perspective. Included within the Objectives for this species is the inclusion of the preferred microHabitat, snags for nesting, within the MSHCP Conservation Area.
MSHCP Conservation Area Configuration Issues
Several large blocks of Habitat that support or potentially support the Williamson's sapsucker will be conserved as Criteria Area and Public/Quasi-Public designations, including the deciduous and montane coniferous forests within the San Bernardino National Forest and Mt. San Jacinto State Park and in areas at lower elevations within San Bernardino National Forest that may be used for wintering. Some areas within the San Bernardino National Forest have not been mapped as being occupied by the Williamson's sapsucker. These Habitat blocks may contain potentially suitable Habitat and could be occupied by Williamson's sapsuckers in the future.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 34,020 acres of suitable Conserved Habitat and will include the preferred microHabitat composed of groups of snags. The current population size of this species is not known and data on point localities is very low.
INCIDENTAL TAKE
About 12,270 acres (27 percent) of potential Habitat for the Williamson's sapsucker will be outside the Criteria Area or Public/Quasi-Public designations, and individuals within this Habitat will be subject to Incidental Take consistent with the plan. Of this, approximately 890 acres (2 percent) of potential Habitat are located within Rural/Mountainous designation areas. This does not represent a significant contribution to the conservation of the Williamson's sapsucker and the areas are located outside of the important breeding Habitat for the species.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The location database for the Williamson's sapsucker includes five data points dated from 1916 through 1998. The more recent records vary in level of mapping precision. Those recorded for the forest service lands are low precision but represent occurrence within the forest areas. Two data records are of high precision within the Prado Basin/Santa Ana River area and represent possible nomadic movements. No additional information in the UCR database is available with which to judge the current status within Western Riverside County. The literature for the southern California area documents that it is a fairly common but local resident in the high elevation areas of the Plan Area (Garrett and Dunn 1981).
A low-to-moderate amount of literature is available for the Williamson's sapsucker, mostly relating to general natural history and the woodpecker family in general. Few controlled scientific studies have been conducted and little management information is available, although some information is available on managing cavity nesters due to the interest of ornithologists in the restrictions placed on the cavity nesting group of birds. Very little information is available for the Plan Area other than what is available regarding basic distribution information.
Habitat and Habitat Associations
Throughout its range, the Williamson's sapsucker breeds at middle to high elevations in montane spruce-fir, Douglas fir, lodgepole pine, and ponderosa pine forests and also may occur in mixed deciduous-coniferous forest with quaking aspen (Dobbs et al. 1997). This species is known from pine Habitats of several types (lodgepole, aspen, Jeffery and eastside) generally between 1,500-3,200 meters (Dobbs et al. 1997; Zeiner, et al. 1990). One study showed the sapsucker prefers Fomes-infected aspen, while another shows the Williamson's sapsucker prefers lodgepole pine, white fir, red fir and Jeffrey pine (in that order) within dry lodgepole, lodgepole-meadow and pine fir Habitats (Crockett and Hadow 1975; Raphael and White 1984). The bird typically inhabits forests with large trees and sparse to moderate canopy cover (Zeiner et al. 1990). Raphael and White (1984) observed 40 percent of nesting in snags and 58 percent using the dead portion of live trees. Williamson's sapsucker nests in tree cavities, possibly for several years (Zeiner et al. 1990). Within southern California, the Williamson's sapsucker is documented to breed in the higher elevations in coniferous forests dominated by lodgepole pines and firs down to the upper border of the yellow pin/Jeffrey pine belt (Garrett and Dunn 1981).
During the non-breeding season, individuals may occupy a wider variety of conifers (Garrett and Dunn 1981). In the southwestern United States, the winter Habitat consists of low-to mid-elevation forests of oak-juniper and pine-oak forests and, to a lesser extent, deciduous riparian and oak forests (Bock and Larson 1986).
Biogeography
The Williamson's sapsucker occurs as a summer resident from southern British Colombia, south through the Cascades, Sierras and Rockies of the western U.S. (Terres 1980). Its distribution appears somewhat disjunct and is described as occurring at middle to high elevation generally between 1,500 and 3,200 meters in several regions including the Pacific Northwest, northern U.S. Rocky Mountains, southern U.S. Rocky Mountains, the Great Basin, and in Mexico (Dobbs et al. 1997).
Within California, there are several disjunct breeding populations of Williamson's sapsucker in the mountains of southern California west of the Mojave Desert, including San Gabriel, San Bernardino, and San Jacinto Mountains and at Mount Pinos. Large concentrations of breeding birds are thought to occur on the north-facing slopes of the San Bernardino Mountains, behind Big Bear Lake near Mount San Gorgonio (Garrett and Dunn 1981). There is a major breeding range within the Sierra Nevada-Cascade ranges from the Greenhorn Mountains north to Oregon; and isolated breeding populations in the extreme north in Siskiyou, Trinity, and Warner Mountains, East Warner Mountains, Sweetwater Range, Carson Range, Ruby and Pequop Mountains, Spruce Mountain, and the Snake Range (Dobbs, et al. 1997).
Wintering Habitat occurs at lower elevations in the southern portions of the above mentioned locations and in northern Baja California, Mexico, northwestern Mexico, and western Texas (Terres 1980). In most of California, the breeding populations are generally resident but there is some regular movement to mid-elevations and irregularly or casually to lowlands surrounding the breeding areas from September to April (Dobbs et al. 1997).
Historic distribution studies have noted that the Williamson's sapsucker has expanded its range westward, resulting in increased abundance in parts of British Columbia (Dobbs et al. 1997).
Known Populations with Western Riverside County
In southern California Williamson's sapsucker is found in the San Bernardino and San Jacinto Mountains between 1,650 and 3,000 meters (Zeiner et al. 1990). It is not recorded within the Santa Ana Mountains. It may move to lower elevation areas for the winter. Some populations within southern California winter within the breeding range as noted above.
There are no documented core areas within the Plan Area within the UCR database. Within the Plan Area, three records are located within the San Bernardino National Forest in the San Jacinto Mountains bioregion. Based on the literature, it is likely that a population is present within the San Bernardino Mountains and the San Jacinto Mountains within the Plan Area.
Biology
Genetics: Relationships of the Sphyrapicus genus, including Williamson's sapsucker, were examined by mt DNA sequencing (Cicero and Johnson 1995). Williamson's sapsucker, the species thyroideus, is the most divergent member of the genus from the standpoint of plumage pattern and degree of sexual dimorphism, and is strongly differentiated genetically from all other members of the genus. In addition, thyroideus was determined to be more closely related to the ancestral species (Cicero and Johnson 1995). The genetic distance of S. thyroideus and other species of the genus Sphyrapicus indicates that thyroideus is as different from its congeners as are species of different genera in the Parulidae (Johnson and Zink 1983).
Diet and Foraging: Williamson's sapsuckers feed on sap, cambium and soft tissues of several coniferous trees exclusively during the prenesting period (Dobbs et al. 1997). The species also eats insects which reside on or in these trees primarily through gleaning and primarily during and after the breeding season (AOU 1997; Raphael and White 1984). Hymenopterans, mainly ants, are the most common food of the Williamson's sapsucker during the breeding season (Otvos and Stark 1985).
Foraging of Williamson's sapsucker mainly occurs in conifers and snags, rarely in aspen, favoring living pines during the breeding and nonbreeding seasons. Trees used for foraging had an average diameter at breast height of 41 centimeters and height of 21 meters in a site in Oregon. Foraging heights range from low-level bare trunk to tree crown with no season differences in height of tree for foraging. In California, lodgepole pine is preferred but the species will forage on hemlock, white fir, Jeffrey pine and aspen (Dobbs et al. 1997).
Daily Activity: The Williamson's sapsucker is a year-long diurnally active species (Zeiner, et al. 1990).
Reproduction: Heartwood decay was the most important factor in nest tree selection by primary cavity-nesting birds in Douglas-fir forests including the congener Sphyrapicus varius (Harestad and Keisker 1989). The Williamson's sapsucker requires snags or live trees with rotted heartwood in which to excavate nesting and roosting cavities (Zeiner et al. 1990). Nesting occurs within tree cavities which may be occupied by the same mating pair (Williamson's sapsucker is a monogamous bird) for several years (Zeiner et al. 1990). They prefer to nest in tall aspen snags, with particularly large live aspen and aspen snags in the surrounding area, near the bottom of snow-melt drainages with 0 to 20 percent of the canopies dominated by aspen (Conway and Martin 1993). The average nest height was 2.4 meters in Colorado, and 13.1 meters in Arizona which correlated with the nest tree height but not the nest tree diameter (Dobbs et al. 1997).
Egg laying of Williamson's sapsucker occurs in late May to mid July and sometimes includes a double brood (Zeiner et al. 1990). The clutch size is usually 4 to 6 eggs and averages 4.38 eggs per nest (Dobbs et al. 1997). Incubation begins before the clutch is complete lasting for 12 to 14 days. Departure from the nest occurs 31 to 32 days after hatching and usually requires 1 to 2 days for the entire brood to leave the nest. Adults quickly disperse after the young leave the nest and males often abandon the young 1 to 2 days before they fledge (Dobbs et al. 1997).
Survival: Nesting success of Williamson's sapsuckers was high in a mixed conifer forest in Arizona at 93.2 percent nest success (Conway and Martin 1993). Successful nests in Arizona fledged an average of 3.67 young; hatching failure and/or nestling mortality was calculated as 1.33 young per nest (Dobbs et al. 1997).
Dispersal: It is thought that the Williamson's sapsucker may migrate downslope or wander during the winter (Zeiner et al. 1990). The Williamson's sapsucker often returns to the same territory and even the same nest tree, year after year (Dobbs et al. 1997).
Socio-Spatial Behavior: Home range for Williamson's sapsucker has been found to be equal to the territory defended, averaging 16.9 acres (Crockett and Hadow 1975). Territories have been estimated from 4-7 hectares (Dobbs et al. 1997). Breeding density was found to be 2.2-8.2 per 100 acres (Zeiner et al. 1990).
Community Relationships: Competition may occur between Williamson's sapsucker and other sapsucker species over territory and nest sites (Raphael and White 1984). The species experience high predation during the immature stage from Accipiter hawks (Dobbs et al. 1997).
Threats to Species
Williamson's sapsucker populations have declined throughout their range from 1982 to 1991, with particularly strong declines in the Pacific Northwest (Dobbs et al. 1997) from Habitat loss.
Special Biological Considerations
Williamson's sapsuckers have narrow Habitat requirements because they require snags or soft wood for excavating nesting cavities and mixed coniferous-deciduous forests of western North America. They are sensitive indicators in intensively managed forest Habitats of western North America (Conway and Martin 1993, Dobbs et al. 1997).
The species may be tolerant of humans in close proximity and to a relatively high level of disturbance.
Heartwood decay was the most important factor in nest tree selection by primary cavity-nesting birds in Douglas-fir forests including the congener Sphyrapicus varius (Harestad and Keisker 1989). This selection preference was confirmed for the Williamson's sapsucker by Schepps et al. (1999). In their study, Williamson's sapsucker chose nest trees that were softer than neighboring or random trees and chose softer trees than the red-naped sapsucker and hairy woodpecker. They concluded that the species is sensitive to subtle characteristics of trees that reflect hardness some of which may not be apparent in the external appearance of the tree (Schepps et al. 1999).
In the Pacific Northwest, 371 snags of at least 30.5 centimeters dbh per 100 hectares are necessary to support a maximum population (Thomas et al. 1979). Forest management plans should emphasize conservation of groups of large snags, rather than random assortments of variable sized snags. Patches of snags and areas of high snag density should be preserved, especially those in drainage bottoms or other low-lying areas. The sites selected for nests had high snag densities in the surrounding area and these snag densities exceeded those commonly used in forest management plans (Conway and Martin 1993). Effective snag management should concentrate snags in groups within low-lying areas and conserve large-sized snags (Conway and Martin 1993). Fire in mixed coniferous forests that creates snags may increase the breeding densities. The availability of sap trees, often large conifers, also should be important (Dobbs et al. 1997).
A Habitat Suitability Index (HSI) correctly predicted that Williamson's sapsuckers should generally prefer drainages over ridgetops but the model could not distinguish between use and non-use sites within drainages. Thus future HSI models for this species should continue to stress snag density but should consider aspen snag density separately from density of other snags, incorporate height and diameter of aspen snags and use a more liberal definition of aspens contributing to overstory canopy cover (Conway and Martin 1993).
LITERATURE CITED
American Ornithologists' Union. 1957. Checklist of North American birds. 5th edition. Lord Baltimore Press, Baltimore, MD. 691 pp.
Bock, C. E., and D. L. Larson. 1986. Winter Habitats of sapsuckers in southeastern Arizona. Condor 88: 246-247.
Cicero, C. And N. K. Johnson. 1995. Speciation in sapsuckers (Sphyrapicus): III. Mitochondrial-DNA sequence divergence at the cytochrome-B locus. Auk 112: 547-563.
Conway, C. J. And T. E. Martin. 1993. Habitat suitability for Williamson's sapsuckers in mixed conifer forests. J. Wildlife Management 57: 322-328.
Crockett, A. B. and H. H. Hadow. 1975. Nest site selection by Williamson's and red-naped sapsuckers. Condor 77:365-368.
Dobbs, R.C., T. E. Martin, and C. J. Conway. 1997. Williamson's sapsucker (Sphyrapicus thyroideus). In The Birds of North America, No. 285 (A. Poole and F. Gill, eds.). The Academy of Natural Sciences, Philadelphia, and The American Ornithologists' Union, Washington, D.C.
Garrett, K. and J. Dunn. 1981. Birds of southern California. Los Angeles Audubon Society. 408pp.
Harestad, A. S. And D. G. Keisker. 1989. Nest tree use by primary cavity-nesting birds in south central British Columbia. Canadian Journal of Zoology 67: 1067-1073.
Johnson, N. K., and R. M. Zink. 1983. Speciation in sapsuckers (Sphyrapicus): I. Genetic differentiation. Auk 100: 871-884.
Miller, A. H. and R. C. Stebbins. 1964. The lives of desert animals in Joshua Tree National Monument. University of California Press, Berkeley. 452pp.
Otvos, I. S. And R. W. Stark. 1985. Arthropod food of some forest-inhabiting birds. Canadian Entomologist 117: 971-990.
Raphael, M. G. and M. White. 1984. Use of snags by cavity-nesting birds in the Sierra Nevada. Wildlife Monographs No. 86, 66pp.
Schepps, J., S. Lohr, and T. E. Martin. 1999. Does tree hardness influence nest tree selection by primary cavity nesters? Auk 116: 658-665.
Thomas, J. W., R. G. Anderson, C. Maser, and E. L. Bull. 1979. Wildlife Habitat in managed forests: the Blue Mountains of Oregon and Washington (J. W. Thomas, ed.). U. S. Dept. Agric. For. Service. Agric. Handbook 533.
Terres, J. K. 1980. The Audubon Society Encyclopedia of North American Birds. Alfred A. Knopf, New York, New York. 1109pp.
Zeiner, D.C., W. F. Laudenslayer, K. E. Mayer and M. White eds. 1990. California's Wildlife: Volume II - Birds. California Department of Fish and Game. Sacramento, California. 732pp.
Wilson's warbler (Wilsonia pusilla)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
Wilson's warbler (Wilsonia pusilla)
Status:
State: None
Federal: Partners in Flight Priority Bird Species; San Bernardino National Forest Sensitive
GROUP DESIGNATION AND RATIONALE
Group 1
The Wilson's warbler has a sparse and widespread distribution within almost every Habitat that occurs within the MSHCP Plan Area. Although few documented records exist for the Wilson's warbler within the Plan Area, the literature suggests that the species forages within the lowland and foothills Bioregions of the Plan Area in almost every Habitat as a transient in the spring and fall and breeds within the mountain Bioregions in shrub and scrub Habitat, wet and montane meadow, and edges of riparian and forested Habitats. The Wilson's warbler has not been reported to winter within the Plan Area. Because the Wilson's warbler is opportunistic and widespread during migration and its breeding Habitat requirements are well known, it is classified as a Group 1 species.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 198,850 acres of suitable montane meadow, riparian scrub, oak woodland and forest, coastal sage scrub, chaparral, and Riversidean alluvial fan sage scrub within the San Bernardino Mountains, San Jacinto Mountains, and Santa Ana Mountains Bioregions.
Objective 2
Include within the MSHCP Conservation Area at least 192,140 acres of suitable dispersal and migration Habitat and interconnecting Linkages within the MSHCP Conservation Area for transient migration movements including grassland, Riversidean alluvial fan sage scrub, coastal sage scrub, desert scrubs, chaparral, peninsular juniper woodland and scrub, riparian scrub, woodland, and forest, and oak woodland and forest.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
For the purpose of the conservation analysis, potential Habitat for breeding for the Wilson's warbler includes montane meadow, montane deciduous woodland, montane chaparral and scrub, and montane riparian scrub, woodland, and forest. The woodland Habitats represent Habitats that contain subsets of Habitats that are suitable for Wilson's warbler including the edges of forested areas and the scrubby and shrubby understory. For transient spring and fall migratory movements through the lower elevation areas, potential Habitat includes lowland and foothill grassland, Riversidean alluvial fan sage scrub, coastal sage scrub, desert scrubs, chaparral, Peninsular juniper woodland and scrub, riparian scrub, woodland, and forest, and oak woodland and forest. Based on these Habitats, the Plan Area supports approximately 269,880 acres of potential breeding Habitat and 411,820 acres of potential migration Habitat for the Wilson's warbler. Table 1 shows the conservation and loss of potential Habitat for the Wilson's warbler. Overall, approximately 198,850 acres (74 percent) of potential breeding Habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public Lands. Approximately 192,140 acres (47 percent) of potential transient migration Habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public Lands.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
WILSON'S WARBLER
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP ConservationArea | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| Breeding Habitat - San Bernardino Mountains, San Jacinto Mountains, and Santa Ana Mountains Bioregions | |||||||
| Montane Meadow | 490 | 0 | 80 | 80 | 20 | 390 | 410 |
| Chaparral | 221,800 | 12,030 | 154,550 | 166,580 | 28,620 | 26,600 | 55,220 |
| Coastal Sage Scrub | 16,650 | 1,870 | 6,790 | 8,660 | 6,500 | 1,490 | 7,990 |
| Riversidean Alluvial Fan Sage Scrub | 1,410 | 320 | 710 | 1,030 | 60 | 320 | 380 |
| Riparian Scrub, Woodland, Forest | 1,960 | 200 | 1,330 | 1,530 | 200 | 230 | 430 |
| Woodlands and Forest | 27,570 | 1,280 | 19,690 | 20,970 | 4,060 | 2,540 | 6,600 |
| Breeding Habitat SUBTOTAL | 269,880 | 15,700 (6%) |
183,150 (68%) |
198,850 (74%) |
39,460 (15%) |
31,570 (12%) |
71,030 (26%) |
| Transient Movement Habitat (Migration) - Riverside Lowlands and San Jacinto Foothills | |||||||
| Grassland | 121,750 | 17,470 | 16,130 | 33,600 | 7,000 | 81,150 | 88,150 |
| Chaparral | 132,080 | 45,820 | 24,170 | 69,990 | 30,760 | 31,330 | 62,090 |
| Coastal Sage Scrub | 133,110 | 43,690 | 27,200 | 70,890 | 19,740 | 42,480 | 62,220 |
| Desert Scrubs | 2,230 | 2,160 | 0 | 2,160 | 40 | 30 | 70 |
| Peninsular Juniper Woodland and Scrub | 930 | 340 | 180 | 520 | 0 | 410 | 410 |
| Riparian Scrub, Woodland, Forest | 12,210 | 3,570 | 5,860 | 9,430 | 180 | 2,600 | 2,780 |
| Riversidean Alluvial Fan Sage Scrub | 5,430 | 2,710 | 1,310 | 4,020 | 160 | 1,250 | 1,410 |
| Woodlands and Forests (oak) | 4,080 | 1,020 | 510 | 1,530 | 920 | 1,630 | 2,550 |
| Migration Habitat SUBTOTAL | 411,820 | 116,780 (28%) |
75,360 (18%) |
192,140 (47%) |
58,800 (14%) |
160,880 (39%) |
219,680 (53%) |
| TOTAL | 681,700 | 132,480 (19%) |
258,510 (38%) |
390,990 (57%) |
98,260 (14%) |
192,450 (28%) |
290,710 (43%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
This species breeds within Forest Service lands within montane meadows, scrub and shrub Habitats, and deciduous woodland Habitats. Within the woodland Habitats, the potential Habitat for Wilson's warbler is a subset and includes those openings and the understory layer that provides the nesting Habitat of the species. Under the existing Forest Land allocation plan, these Habitats generally are located within the San Jacinto and San Mateo Canyon wilderness areas as well as in most of the grazing allotments.
In addition to the above protection, the Riparian/Riverine Areas and Vernal Pools policy described in Section 6.1.2 (MSHCP Volume 1) provides for conservation of wetlands through avoidance and minimization. Higher-elevation wetlands provide foraging and breeding Habitat for this species. Mitigation for impacts to wetlands will be incorporated in accordance with the "No Net Loss" policy of federal and state wetland regulations. The proposed mitigation will be directly related to the functions and values of the wetland as related to this species and result in equivalent replacement. This policy may also provide some protection for foraging Habitat of the Wilson's warbler in the lowland riparian areas and in breeding Habitat composed of montane meadow and wet meadow Habitat.
Rural/Mountainous Designation Areas
As depicted on the MSHCP Plan Map (Figure 3-1, MSHCP Volume 1), certain areas adjacent to the MSHCP Conservation Area are designated as Rural/Mountainous in the County's General Plan. These areas are generally constrained for development due to steep topography and the level of development in these areas is anticipated to be of rural residential character with 1 DU/10, 20, or 40 acres, depending on slope. While these areas will not be included within the MSHCP Conservation Area, managed for the benefit of species conserved under the MSHCP, and the existing zoning/ordinances for these areas do not preclude development and could allow substantial fragmentation and/or degradation of Habitat for proposed covered species, the low levels of development anticipated in these areas may provide an edge to the MSHCP Conservation Area that may be of value to the Wilson's warbler.
For the Wilson's warbler, conservation of portions of the Santa Rosa Plateau may be important for maintaining connection between the Santa Rosa Plateau Nature MSHCP Conservation Area and the Santa Ana Mountains or lowland foraging areas. MSHCP Conservation Area locations in these areas are generally surrounded by lands designated as Rural/Mountainous. Potential development in these areas is anticipated to retain vacant areas that provide for seasonal movement for this species. A total of 58,800 acres (14 percent) of potential transient migratory movement Habitat for the Wilson's warbler will be designated Rural/Mountainous. In addition, 39,460 acres (15 percent) of potential breeding Habitat will be designated Rural/Mountainous.
As described above under Data Characterization, 29 of the 69 relatively recent point localities have high precision. Of these 29 point localities, 9 will be inside the Criteria Area and 9 will be located within Public/Quasi-Public Lands. Of the 11 high precision recent points located outside the MSHCP Conservation Area, all are located in non-native grassland or developed areas except two points which are located within sage scrub. These locations were all recorded during migration. The data point locations are probably under-represented due to lack of surveys and reporting. Wilson's warbler is observed frequently especially during migration but has also been documented in the national forest areas nesting in meadow and at edges of conifers adjacent to open pockets of meadow (Hayworth, 1992, pers. obs.). Conservation of this species will be considered from a landscape perspective due to the fact that the suitable nesting Habitat has been well defined and the species uses a large variety of foraging Habitats during migration movements. Providing additional suitable Habitat that is not currently known to be occupied may assist with the recovery of the species. In addition, there are definable locations for focusing conservation efforts including breeding Habitat in the San Jacinto Mountains, San Bernardino Mountains and possibly the Santa Ana Mountains, and migratory stopover areas at the Prado Basin and Santa Ana River and other potential suitable stopover locations at Temescal Wash, Lake Mathews-Estelle Mountain, Sedco Hills, Santa Rosa Plateau, Vail Lake/Wilson Valley, Temecula, Murrieta, and Tucalota creeks, Motte-Rimrock Reserve, the Badlands, Sycamore Canyon Regional Park, and Box Springs.
MSHCP Conservation Area Configuration Issues
Several large blocks of Habitat supporting or potentially supporting the Wilson's warbler will be conserved as Criteria Area and Public/Quasi-Public designations, including breeding Habitat within the San Bernardino Mountains, the San Jacinto Mountains, and the Santa Ana Mountains, migratory stopover areas at the Prado Basin and Santa Ana River, and other potential stopover locations at Temescal Wash, Lake Mathews-Estelle Mountain, Sedco Hills, Santa Rosa Plateau, Vail Lake/Wilson Valley, Temecula, Murrieta, and Tucalota creeks, Motte-Rimrock Reserve, the Badlands, Sycamore Canyon Regional Park, and Box Springs. Some of the large blocks of Habitat have not been mapped as containing Wilson's warblers. However, these Habitat blocks have suitable foraging Habitat and within the higher elevations contain suitable breeding Habitat. As a long-distance migrant, Wilson's warblers are likely able to discover and use patches of Habitat that have not been documented to be used in the past. As such, the MSHCP Conservation Area will provide adequate blocks of a variety of upland and riparian Habitat as stopover areas for this species and will provide large patches of higher elevation Habitat composed of meadow, deciduous and conifer woodlands for potential nesting areas.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 198,850 acres of suitable Conserved Habitat including the breeding Habitat composed of montane meadow, chaparral, coastal sage scrub, Riversidean alluvial fan sage scrub, riparian scrub, woodland, and forest, and oak woodlands and forest. In addition, at least 192,140 acres of suitable Conserved Habitat including the transient/migration Habitat are included in the MSHCP Conservation Area. The MSHCP Conservation Area has been designed to preserve the large blocks of areas that contain a variety of potentially suitable Habitats for foraging use during migration as well as very large blocks that contain potentially suitable nesting Habitat for the species.
INCIDENTAL TAKE
The Incidental Take of the Wilson's warbler is difficult to quantify due to our limited knowledge of its distribution and abundance within the Plan Area. The maximum level of Incidental Take of Wilson's warblers can be anticipated by the loss of the number of acres of potential Habitat that will become unsuitable for this species. About 71,030 acres (26 percent) of potential breeding Habitat for the Wilson's warbler will be outside the Criteria Area and Public/Quasi-Public Lands designations and individuals within these areas will be subject to Incidental Take consistent with the Plan. Of this, approximately 39,460 acres (15 percent) will be within Rural/Mountainous designation areas. About 219,680 acres (53 percent) potential transient migratory movement Habitat for the Wilson's warbler will be outside the Criteria Area and Public/Quasi-Public Lands designations. Of this, approximately 58,800 acres (14 percent) will be within Rural/Mountainous designation areas. Although these areas will not be part of the managed MSHCP Conservation Area, the anticipated levels of development in these areas may be consistent with the continued presence of the Wilson's warbler.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The location database for the Wilson's warbler includes approximately 88 location records for western Riverside County. These record locations are dated from 1887 to 1999 with approximately 69 dated recently from 1990 through 1999. A total of 29 of the more recent records are of high precision and may accurately indicate the location and Habitat of the record. Most of the high precision, recent records are located within riparian, sage scrub, chaparral, and non-native grassland Habitats. Twelve of these records are located within residential/urban lands and may no longer be extant. Only one recent record is located within a montane Habitat thus the balance of the records represent migratory birds and not breeding individuals.
A low-to-moderate amount of literature is available for the Wilson's warbler, mostly relating to natural history and warblers in general. Few controlled scientific studies have been conducted and little management information is available. Very little information is available for the Plan Area other than what is available regarding basic distribution information.
Habitat and Habitat Associations
Breeding Habitats for the Wilson's warbler include montane meadows and low, dense willow thickets as well as other shrubs and scrub, often on steep slopes (Garrett and Dunn 1981). It nests in the Arctic up to the limit of trees and typically nests in Habitats such as thickets, second-growth saplings or clearings, in spruce-tamarack, balsam fir, and sphagnum bogs, or in alders and birches near streams and ponds (Terres 1980). The western montane, northern, and northeastern populations are restricted to mesic shrub thickets of woodland Habitats, the edges of beaver ponds, lakes, bogs, and overgrown clear-cuts of the montane and boreal zone (Ammon and Gilbert 1999). The Pacific coast populations use a variety of mesic shrub Habitats in humid coastal forests, such as clear-cuts, shrub thickets, and stands of young conifers, alders, and maples. The pacific coast birds also breed in the dryer scrub Habitats consisting of coyote bush and blackberry mixed with Douglas fir, in shrub understory of the forests. The abundance is positively correlated with the amount of deciduous tree and shrub cover (Ammon and Gilbert 1999).
Outside of the breeding season, during migration, these birds can be seen passing through woodlands and forests with shrub understories as well as chaparral Habitats, and it also may occur in well-grown woodlands, city parks, and gardens (Terres 1980; Zeiner et al. 1990). It occurs in most deciduous shrub Habitats as well as riparian understory (Ammon and Gibert 1999). The congener, hooded warbler (Wilsonia citrina), shows a significant Habitat segregation by sex on their wintering grounds in Mexico with the males choosing forest Habitat and females choosing shrub or field Habitats (Morton 1990; Lopez-Ornat and Greenberg 1990). In migration over desert Habitats, birds can use almost any available vegetation but mostly forage near the ground (Miller and Stebbins 1964). Habitat use differed between spring and fall migration and was affected by the combination of age and sex. Wilson's warblers appear to prefer native willow Habitat during spring migration (Yong, et al. 1998). Agriculture field/edge Habitats may have represented sink Habitats because birds in these Habitats tended to be immature and had a lower rate of fat deposition and longer stopovers (Yong, et al. 1998).
Biogeography
The breeding range for the species is relatively large, extending from northern Alaska, east to Newfoundland, south to southern California into northern New Mexico and northern New England (Terres 1980). The wintering Habitat begins in southern Baja California, Mexico and southern Texas to Panama (Terres 1980).
In California, the majority of the range is occupied by summer migrants and extends along the coast and in the Sierras (Zeiner et al. 1990). The winter range extends into San Diego, Orange, Los Angeles, Ventura and Santa Barbara counties along the coast (Garrett and Dunn 1981). Wilson's warblers are migratory, arriving from Mexico in mid-April through early May. Fall migrants arrive in mid-August and remain into late fall and occasionally can be seen in early December (Unitt 1984).
Significant declines appear to have occurred in southern California where, within historic times, extensive populations were extirpated due to riparian Habitat loss, urbanization, and possiby cowbird parasitism. Before the extirpation, the Wilson's warbler was a common breeder along the coastal streams in Los Angeles area and south to San Diego (Ammon and Gilbert 1999).
Known Populations Within Western Riverside County
Inland occurrences in southern California are all summer migrants and occur in three areas in western Riverside, southwestern San Bernardino and eastern Los Angeles counties (Zeiner, et al. 1990). Within western Riverside County, the Wilson's warbler is a common transient throughout the spring and less common during the fall (Garrett and Dunn 1981). There are no records extending through the winter (Garrett and Dunn 1981). The species currently breeds around montane meadows within the San Bernardino Mountains and the San Jacinto Mountains within the eastern portion of western Riverside County (Garrett and Dunn 1981).
Geographic locations recorded within the U.C. Riverside database include: Cleveland National Forest and San Bernardino National Forest for breeding locations, Prado Basin, Santa Ana River, Temescal Wash, Murrieta Creek, Temecula Creek, Wilson Creek, Wildomar, Santa Rosa Plateau, Lake Matthews, Lake Perris, Mystic Lake/San Jacinto Wildlife Area, Motte-Rimrock Reserve, Box Springs Mountains, Sycamore Canyon Regional Park, Bautista Creek, Gavilan Hills, Quail Valley, March ARB, Badlands, and San Timoteo Creek for wintering or transient migrant locations.
Biology
Genetics: Three subspecies of the Wilson's warbler are recognized. These subspecies differ slightly in size and plumage coloration and pattern (Ammon and Gilbert 1999). Evidence from mtDNA sequence data suggests two major lineages of the Wilson's warbler with all western populations more closely related to each other than to eastern populations. The genetic subdivision within the western group may exist between coastal and interior populations thus not corresponding to the current taxonomic division based on phenotypic characters (Ammon and Gilbert 1999).
Diet and Foraging: Bent (1953) reports that 93 percent of the food intake of the Wilson's warbler consists of animal matter, based on a sample of 53 birds, as well as small amounts of seeds, berries, and other fruits (Zeiner, et al. 1990). Wilson's warblers are selective in the sizes of prey they consume with smaller prey being under-represented in their diets (Raley and Anderson 1990). In the same study, the food group chosen most often were Coleptera of which beetles with soft elytra are a major component (Raley and Anderson 1990). Arthropods that ranked high in preference for warblers are noncrytic and patchy in distribution (Raley and Anderson 1990). The species forages by gleaning for invertebrate prey, usually within 10 feet of the ground; it may forage by flycatching for insects in the lower canopy (Terres 1980; Zeiner et al. 1990).
Daily Activity: The Wilson's warbler shows a year-long diurnal activity with nocturnal migratory activity (Zeiner et al. 1990).
Reproduction: Wilson warbler's breed from late April to early August and they are monogamous (Harrison 1951). Pairs typically nests near water or meadows, within 1 meter of the ground or on the ground, under dense shrub cover (Zeiner et al. 1990). The nest is a bulky structure, sunken in moss or sedges, sometimes at the base of alders, and is built of mosses, dead leaves, fine weed stalks, grasses, and is lined with finer grasses (Terres 1980). The species may nest in loose colonies (Terres 1980). The female Wilson's warbler has been documented to sing after pair formation has taken place (Gilbert and Carroll 1999). This song seemed to serve as a simple contact vocalization between the mates, similar to call notes and may also aid in pair formation (Gilbert and Carroll 1999). Eggs are laid in April in California to June or July in Alaska and number four to six, commonly five; incubation is 10 to 11 days and the young leave the nest when 10 to 11 days old (Terres 1980; Bent 1953).
Survival: The numbers of adult and hatching-year Wilson's warblers captured each year shows no consistent trend through time (Chase et al. 1997). The total number of adults captured annually, an index of adult abundance, was positively related to productivity in the previous year (Chase et al. 1997). Estimated annual adult survival of summer residents was 50.3 percent and the annual recapture probability for summer residents was much greater than for presumed transients at 68.8 percent versus 7.2 percent, respectively (Chase et al. 1997). These patterns of survival and productivity parameters suggest that abundance in this population has been influenced primarily by circumstances on the breeding grounds (Chase et al. 1997).
Dispersal: The Wilson's warbler apparently wanders during the post-breeding season. This nomadic wandering probably occurs after breeding or attempted breeding during the time when territoriality is waning. This is correlated with an unrestricted search for food in preparation for molt and migration to increase the chance of survival during the post breeding period (Stewart 1973). Studies on the dispersal and re-nesting location sites of the congener, hooded warbler, indicate that the greater dispersal of successful females was due to their avoidance of fledglings that remained near the nest with the male, whereas females that suffered predation of the first nest located the second nest in close proximity (Howlett and Stutchbury 1997).
Socio-Spatial Behavior: The home rangeof the Wilson's warbler in Marin County was reported at 125-300 meters from the nest while territory size averaged 0.5 hectares (Stewart 1973).
Community Relationships: The Wilson's warbler is subject to predation from accipiters, small mammals and snakes (Zeiner et al. 1990).
Threats to Species
Brown-headed cowbirds regularly parasitize the Wilson's warbler and may be partially responsible for extirpation from lowland areas (Garrett and Dunn 1981). Studies on cowbird parasitism of the congener, hooded warbler, show that cowbird trapping reduced parasitism from 53 percent to 10 percent but did not increase the number of young fledged per nest due to increased predation in the cowbird controlled populations (Stutchbury 1997). This suggest that removal of cowbirds as a management tool may have minimal benefits for this congeneric species (Stutchbury 1997). Whether this relationship also applies to the Wilson's warbler is unknown.
On the breeding grounds, the Wilson's warbler is less abundant in 0-10 year old forest clear cuts than in uncut forests, however it is more abundant in 11-20 year old clear cuts than in uncut forests. A decreased abundance is also associated wiht heavy cattle grazing. The degradation of woodland Habitats is likely a major cause of reduced breeding abundances in the western region (Ammon and Gilbert 1999).
Special Biological Considerations
Miller and Stebbins (1964) report observing exhaustion of Wilson's warblers in high temperatures. Studies on migratory behavior of Wilson's warbler reveal that events during migratory stopovers may have significant consequences in determining the population status of migratory songbirds (Yong, et al. 1998). Variation in stopover patterns was predominantly sex related in spring and age related in fall (Yong, et al. 1998). In spring, males appeared at study sites earlier than females and they carried higher fat stores and higher rates of mass gain (Yong, et al. 1998). In fall, migratory passage overlapped temporally among age and sex classes but young birds had lower fat stores and longer stopovers than adults (Yong et al. 1998). The data of Yong, et al. (1998) suggest that immatures were particularly vulnerable to Habitat disturbances at stopover sites during fall migration, probably because of their lower social status and inexperience with long-distance migration. Yong, et al. (1998) concluded that knowledge of intraspecific variation in migration strategies is important for effective management of stopover Habitats for migratory songbirds.
Peak density of Wilson's warbler reached 48 birds per hectare within a patch of cottonwood-willow riparian Habitat along the San Pedro River in Arizona (Skagen et al. 1998). This peak density far exceeded breeding density suggesting that large components of the birds within the area were en route migrants. Skagen et al. (1998) concluded that the protection of both small, disjunct riparian patches and extensive riverine tracts in western landscapes is important.
As indicated in the discussion above, within western Riverside County, the Wilson's warbler occurs in the area during two phases of its life history: as a migrating species in the spring and less common during the fall; and as a breeding summer resident within the montane areas (Garrett and Dunn 1981).
LITERATURE CITED
Ammon, E. M., and W. M. Gilbert. 1999. Wilson's warbler. In The Birds of North America No. 478. A. Poole and F. Gill, Editors. Cornell Laboratory of Ornithology and The Academy of Natural Sciences.
Bent, A. C. 1953. Life histories of North American wood warblers. U.S. National Museum Bulletin 203. 734pp.
Chase, M. K., N. Nur, and G. R. Geupel. 1997. Survival, productivity, and abundance in a Wilson's warbler population. Auk 114: 354-366.
Garrett, K. and J. Dunn. 1981. Birds of southern California. Los Angeles Audubon Society. 408pp.
Gilbert, W. M. And A. F. Carroll. 1999. Singing in a mated female Wilson's Warbler. Wilson Bulletin 111: 134-137.
Harrison, H. H. 1951. Notes and observation on the Wilson's warbler. Wilson Bulletin. 63:143-148.
Hayworth, A. 1992. Pers. Obs. Hayworth Biological Consultant.
Howlett, J. S. And B. J. M. Stutchbury. 1997. Within-season dispersal, nest-site modification, and predation in renesting hooded warblers. Wilson Bulletin 109: 643-649.
Lopez-Ornat, A. And R. Greenberg. 1990. Sexual segregation by Habitat in migratory warblers in Quintana Roo, Mexico. Auk 107: 539-543.
Miller, A. H. and R. C. Stebbins. 1964. The lives of desert animals in Joshua Tree National Monument. University of California Press, Berkeley. 452pp.
Morton, E. S. 1990. Habitat segregation by sex in the hooded warbler: Experiments on proximate causation and discussion of its evolution. American Naturalist 135: 319-333.
Raley, C. M. And S. H. Anderson. 1990. Availability and use of arthropod food resources by Wilson's warblers and Lincoln's sparrow in southeastern Wyoming . Condor 92: 141-150.
Skagen, S. K., C. P. Melcher, W. H. Howe, and F. L. Knopf. 1998. Comparative use of riparian corridors and oases by migrating birds in southeast Arizona. Conservation Biology 12: 896-909.
Stewart, R. M. 1973 Breeding behavior and life history of the Wilson's warbler. Wilson Bulletin. 85:21-30.
Stutchbury, B. J. M. 1997. Effects of female cowbird removal on reproductive success of hooded warblers. Wilson Bulletin 109: 74-81.
Terres, J. K. 1980. The Audubon Society Encyclopedia of North American Birds. Alfred A. Knopf, New York, New York. 1109pp.
Unitt, P. 1984. The birds of San Diego County. San Diego Society of Natural History: Memoir 13, San Diego, California. 276pp.
Yong, W., D. M. Finch, F. R. Moore, and J. F. Kelly. 1998. Stopover ecology and Habitat use of migratory Wilson's warblers. Auk 115: 829-842.
Zeiner, D.C., W. F. Laudenslayer, K. E. Mayer and M. White eds. 1990. California's Wildlife: Volume II - Birds. California Department of Fish and Game. Sacramento, California. 732 pp.
yellow-breasted chat (Icteria virens)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
yellow-breasted chat (Icteria virens)
Status:
State: Species of Special Concern
Federal: Partners in Flight Priority Bird Species; San Bernardino National Forest Sensitive
GROUP DESIGNATION AND RATIONALE
Group 2
The yellow-breasted chat is sparsely and widely distributed throughout the MSHCP Plan Area within suitable Habitat. There appear to be several Core Areas including the Prado Basin/Santa Ana River, Temescal Wash including the Alberhill Creek tributary, Temecula Creek, Vail Lake area, San Timoteo Creek, and Canyon Lake. Because this species is associated with riparian woodland and riparian scrub Habitats, occurs in a wide but sparse distribution in the lowland and foothills areas of the Plan Area within suitable Habitat, but has specific locations that are Core Areas, this species will be managed at a landscape level with site specific requirements.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 9,430 acres of suitable Habitat for the yellow-breasted chat including riparian woodland and riparian scrub Habitat within the Riverside lowlands and San Jacinto Foothills Bioregions.
Objective 2
Include within the MSHCP Conservation Area at least 5 Core Areas including the Prado Basin/Santa Ana River (9,670 acres), Temescal Wash including Alberhill Creek (estimated as Subunit 3 of Temescal Canyon Area Plan plus Proposed Constrained Linkage 6 and Proposed Linkage 2 at 4,290 acres), Temecula Creek (Subunit 2 of Southwest Area Plan; 850 acres), Vail Lake (Subunit 3 of Southwest Area Plan; 12,320 acres), and San Timoteo Creek (Subunit 3 of The Pass Area Plan; 2,290 acres) and maintain adequate Habitat linkages between Core Areas and smaller drainages and tributaries.
Objective 3
Within the MSHCP Conservation Area, maintain (once every 5 years) the continued use of, and successful reproduction at 75 percent of the Core Areas (including any Core Areas identified in the MSHCP Conservation Area in the future). Successful reproduction is defined as a nest which fledged at least one known young.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
For the purpose of the conservation analysis, potential Habitat for the yellow-breasted chat includes riparian woodland and riparian scrub. Potential Habitat for this species occurs within the suitable riparian Habitat located in the Riverside lowlands and San Jacinto Foothills Bioregions. Based on these Habitats, the Plan Area supports approximately 12,210 acres of potential Habitat for the yellow-breasted chat. Table 1 shows the conservation and loss of potential Habitat for the yellow-breasted chat. Overall, approximately 9,430 acres (77 percent) of potential Habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public Lands. It is assumed that these lands will be managed for wildlife resources including the yellow-breasted chat.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
YELLOW-BREASTED CHAT
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| Riverside Lowlands and San Jacinto Foothills Bioregions | |||||||
| Riparian Scrub, Woodland, Forest | 12,210 | 3,570 | 5,860 | 9,430 | 180 | 2,600 | 2,780 |
| TOTAL | 12,210 | 3,570 (29%) |
5,860 (48%) |
9,430 (77%) |
180 (2%) |
2,600 (21%) |
2,780 (23%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
Six Core Areas of the yellow-breasted chat occur within the Plan Area. Conservation efforts will preserve five of those six key populations. The key populations that will be conserved in Criteria Area or Public/Quasi-Public lands include Prado Basin/Santa Ana River, Temescal Wash including the tributary Alberhill Creek, Temecula Creek, Vail Lake, and San Timoteo Creek.
As described below under Data Characterization, 23 of the 50 relatively recent point localities have a precision of "1." Of these 23 point localities, 5 (22 percent) will be inside the Criteria Area and 8 (35 percent) are located within Public/Quasi-Public Lands. A total of 1 point location (4 percent) will be in the Rural/Mountainous zone. Of the 9 high precision recent points located outside the MSHCP Conservation Area, two points are located within suitable Habitat composed of open water/reservoir/ pond or riparian Habitat and the balance are located outside suitable Habitat areas within existing residential/urban/exotic areas, non-native grassland, croplands, or Riversidean sage scrub. It is likely that many of the point locations are within riparian Habitat and some of these may be inside the MSHCP Conservation Area but do not appear to be due to mapping scale. Conservation of this species will be considered from a landscape perspective, especially in the more western lowlands along the Interstate 15 corridor. This is largely due to the fact that the suitable Habitat has been well defined and providing additional suitable Habitat that is not currently occupied may assist with the recovery of the species.
In addition, there are definable locations comprising Core Areas for focusing conservation efforts including Prado Basin/Santa Ana River (9,670 acres), San Timoteo Creek (2,290 acres), Temescal Wash including the Alberhill Creek tributary (estimated as subunit 3 of Temescal Canyon Area Plan plus proposed constrained linkage 6 and proposed linkage 2 at 4,290 acres), Temecula Creek (Subunit 2 of Southwest Area Plan; 850 acres), Vail Lake (Subunit 3 of Southwest Area Plan; 12,320 acres), and San Timoteo Creek (Subunit 3 of The Pass Area Plan; 2,290 acres). The total acreage of Core Areas that are within Criteria Area and Public/Quasi-Public designations is approximately 29,420 acres. In addition, the MSHCP Plan will maintain (once every 5 years) the continued use of, and successful reproduction at 75 percent of the Core Areas (including any Core Areas identified in the MSHCP Conservation Area in the future).
MSHCP Conservation Area Configuration Issues
Several large blocks of Habitat supporting or potentially supporting the yellow-breasted chat, which provide breeding, wintering, and migration Habitat, will be conserved within the Criteria Area or Public/Quasi-Public designations, including the Prado Basin/Santa Ana River, Temescal Wash including the Alberhill Creek Tributary, San Timoteo Creek, Temecula Creek and Vail Lake. Areas not documented as Core Areas but that contain scattered point locations and/or provide potential suitable Habitat within the lowlands and foothills Bioregions include Motte-Rimrock Preserve, Lake Mathews-Estelle Mountain, San Jacinto River, Lake Elsinore, the Badlands, Lake Skinner-Diamond Valley Lake, Mystic Lake/San Jacinto Wildlife Area, Lake Perris, Sycamore Canyon Regional Park, Wilson Valley, Kabian Park, and Potrero Valley. Other more constrained areas are provided protection by the designation as MSHCP Conservation Area including areas that provide potential Habitat for the yellow-breasted chat such as Tucalota Creek and Murrieta Creek. Some of the large blocks of Habitat have not been mapped as containing yellow-breasted chats. However, these Habitat blocks and smaller riparian systems that contain potentially suitable Habitat could be occupied by yellow-breasted chats in the future. The MSHCP Conservation Area will provide adequate Habitat linkages between Core Areas for this species and smaller drainages that may support small numbers of the species. The Prado Basin Core Area is linked along the Santa Ana River to San Bernardino and Orange counties. This riparian area is linked to the south by the Temescal Wash to Lake Mathews and Lake Elsinore. Riparian Habitat within the Vail Lake area is linked to the Lake Skinner/Diamond Valley Lake area via Tucalota Creek. The Vail Lake area is also linked to Temecula Creek, Murrieta Creek, and Wilson Valley and includes Wilson Creek. The Badlands area provides a major Habitat block or proposed core that provides a connection to Potrero Creek and the Lake Perris area and Mystic Lake/San Jacinto Wildlife Area.
Conservation Summary
In summary, conservation for this species will be achieved by the inclusion of at least 9,430 acres of suitable Conserved Habitat and five Core Areas which total 29,420 acres. The MSHCP has been designed to preserve the important Core Area representing the larger known populations at Prado Basin/Santa Ana River as well as four other Core Areas. In addition, the MSHCP Plan will maintain (once every 5 years) the continued use of, and successful reproduction at 75 percent of the Core Areas (including any Core Areas identified in the MSHCP Conservation Area in the future). Successful reproduction is defined as a nest which fledged at least one known young. Preservation of sites containing smaller numbers of yellow-breasted chats are likely to be just as important as the large population sites. These small populations, documented above to be largely preserved are important to prevent further isolation of remaining breeding groups. Additionally, some of these smaller riparian Habitat patches may provide restoration opportunities that are no longer available within some of the larger riparian systems.
INCIDENTAL TAKE
About 2,780 acres (23 percent) of potential Habitat for the yellow-breasted chat will be outside the Criteria Area and Public/Quasi-Public designations, and individuals within these areas may be subject to Incidental Take. A total of one of six Core Areas, the population located at Canyon Lake, will not be conserved within the MSHCP Conservation Area.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The UCR location database contains approximately 60 records for the yellow-breasted chat dated from 1888 to 2000. A total of 50 of these records are relatively recent (within the past 10 years) and of these more recent records, 23 records are of high precision and can be accurately placed within the Plan Area. The Habitat types associated with the high precision and recent records includes residential, riparian, grassland, sage scrub and open water. The residential Habitat records (a total of 9 of the recent and high precision records) may be within small patches of riparian or riparian scrub Habitat adjacent to a residential development or may no longer be extant.
The literature available for the yellow-breasted chat is relatively low and is generally limited to summaries and general natural history information within ornithological reference material.
Habitat and Habitat Associations
Yellow-breasted chats as a whole may nest in second-growth, riparian thickets and brush (AOU 1998). By contrast, yellow-breasted chats in southern California and within the Plan Area are primarily found in dense, relatively wide riparian woodlands and thickets of willows, vine tangles, and dense brush with well-developed understories. Nesting areas are associated with streams, swampy ground, and the borders of small ponds. Grinnell and Miller (1944) suggested that the plant cover in breeding Habitat must be dense to provide shade and concealment.
Biogeography
Yellow-breasted chats as a whole summer and nest from British Columbia eastward to New Hampshire, and southward to Baja California and northern, mainland Mexico. The species presumably migrates throughout much of North America and winters primarily from northern Mexico to Panama (AOU 1998).
Zeiner, et al. (1990) summarize the distribution, abundance, and seasonality of the yellow-breasted chat within California as follows. The yellow-breasted chat is an uncommon summer resident and migrant in coastal California and in the foothills of the Sierra Nevada. The chat is found up to about 1,450 meters (4,800 ft) in valley foothill riparian, and up to 2,050 meters (6,500 ft) east of the Sierra Nevada in desert riparian Habitats (Gaines 1977, DeSante and Ainley 1980, Garrett and Dunn 1981). The yellow-breasted chat is uncommon along the coast of northern California and occurs only locally south of Mendocino County (McCaskie, et al. 1979). In southern California, the species breeds locally on the coast and very locally inland and at lower elevations nearly throughout the region (Garrett and Dunn 1981).
In migration, the yellow-breasted chat may be found in lower elevations of mountains in riparian Habitat (McCaskie, et al. 1979). It usually arrives in April and departs by late September for the wintering grounds in Mexico and Guatemala. The species may also wander upslope during the postbreeding season (Gaines 1977). There are a few late fall and winter records of the yellow-breasted chat, mostly from southern California. Migrants sometimes pass through lower elevations in mountains. Migrants of the species are encountered only rarely to uncommonly away from breeding centers, and there are no confirmed mid-winter records in the region (Garrett and Dunn 1981).
Once considered fairly common to common in California (Grinnell and Miller 1944), the yellow-breasted chat has been more recently judged to be uncommon and local in southern California (Garrett and Dunn 1981).
Known Populations Within Western Riverside County
The yellow-breasted chat apparently is found nearly throughout the Plan Area in appropriate riparian Habitats in the lowlands and lower foothill regions (Garrett and Dunn 1981). The chat likely is found at many of the areas occupied by yellow warblers in the lowlands and foothills (please see yellow warbler species account) (Michael Patten 1998, pers. comm. Riverside County Editor for American Field Notes and Past Secretary, California Bird Records Committee).
The species is generally located within the western portion of the Plan Area from the northwest corner, south along the Interstate 15 corridor to Temecula. Core areas of the yellow-breasted chat include the large concentration in the Prado Basin and contiguous reaches of the Santa Ana River. Other known localities that may represent Core Areas include San Timoteo Creek, Temescal Canyon including the Alberhill Creek tributary, Canyon Lake, Temecula Creek, and Vail Lake. Additional localities include Motte-Rimrock Reserve, San Jacinto River and Potrero Creek.
Biology
Genetics: No information is available or was reviewed.
Diet and Foraging: The yellow-breasted chat eats insects and spiders; it also may take berries and other fruits. Mostly the yellow-breasted chat gleans from foliage of shrubs and low trees (Zeiner, et al. 1990). The feeding rates of adults appears to be unaffected by brood size (Schadd and Ritchison 1998).
Daily Activity: The yellow-breasted chat exhibits year-long, diurnal activity and is a nocturnal migrant (Zeiner, et al. 1990).
Reproduction: Nesting of the yellow-breasted chat occurs in dense plant cover within streams, swampy ground, and the borders of small ponds. In one study, chats were shown to prefer to nest in large Habitat patches and, although this increased their risk of brood-parasitism, it decreased the risk of nest predation and resulted in a higher nesting success (Burhans and Thompson 1999). Yellow-breasted chats have been characterized as a relative generalist in regards to nesting Habitat selection within a riparian area (Brown and Tossett 1989).
The yellow-breasted chat breeds from early May into early August with a peak of nesting activity in June. The nest of the species is usually 0.6 to 2.4 meters (2-8 feet) above the ground in dense shrubs along a stream or river. The yellow-breasted chat is monogamous, although pairs may nest near one another (Ehrlich, et al. 1988). The yellow-breasted chat lays 3-6 eggs, usually 3 or 4 eggs. Incubation is typically 11-15 days; the chicks apparently fledge in 8-11 days. The altricial young are tended by both parents until fledgling (Harrison 1978).
Survival: No information is available or was reviewed.
Dispersal: No information is available or was reviewed.
Socio-Spatial Behavior: Dennis (1958) reported that the home range of the yellow-breasted chat in summer was larger than its territory, but gave no sizes. Gaines (1974a) reported a home range of 10 pairs of the chat per 40 hectares (100 acres) in a Sacramento Valley riparian area. Thompson and Nolan (1973) reported 28 territories averaging 1.3 hectares (3.1 acres) in an abandoned Indiana field. Brewer (1955) reported the territory of the species as averaging 0.12 hectares (0.3 acres), and varying from 0.04 to 0.28 hectares (0.1 to 0.7 acres), in an Illinois swamp thicket. Dennis (1958) reported territory sizes of the yellow-breasted chat varying from 0.5 to 1.0 hectare (1.25 to 2.5 acres) in abandoned fields and along fence rows in Virginia.
Community Relationships: The yellow-breasted chat is susceptible to brood-parasitism by the brown-headed cowbird. The species is subject to occasional predation by accipiters, small mammals, and snakes (Zeiner, et al. 1990).
Threats to Species
The loss and fragmentation of riparian woodlands in the coastal lowland as a result of development, agriculture, and channeling rivers has led to the decline of the yellow-breasted chat. Garrett and Dunn (1981) concluded that the clearing of dense riparian thickets and brush tangles has caused a noticeable decline in the number of breeding pairs of the chat. Cowbird parasitism may have played an additional role in the decline of the yellow-breasted chat affecting its distribution in addition to its density (Gaines 1974, Remsen 1978).
Special Biological Considerations
The yellow-breasted chat has not noticeably increased within the Prado Basin during the course of 14 years of cowbird management and Habitat conservation efforts there (USFWS 1999, unpublished data). However, by contrast, there is no evidence that the species has decreased during that same time frame. The Prado Basin/Santa Ana River yellow-breasted chat population was relatively large and stable prior to the onset of management efforts within the area (USFWS 1999, unpublished data).
A study of riparian stopover sites in southeast Arizona illustrates the importance of these wetland features to migratory birds including the yellow-breasted chat (Skagen, et al. 1998).
A study of various type of forest regeneration practices (clear-cut, shelter wood, group-selection and single tree selection found that yellow-breasted chats were most abundant in clear-cut forests that were regenerating (Annand and Thompson 1997).
Low-level grazing of cottonwood bottomland in northeastern Colorado was found to be compatible with migratory use of the yellow-breasted chat, although the researchers warn that this species is most likely to respond negatively to increases in grazing activity (Sedgwick and Knopf 1987).
LITERATURE CITED
AOU (American Ornithologists' Union). 1998. Check-List of North American Birds. Seventh Edition. American Ornithologists' Union, Washington, D.C. 829 pp.
Annand, E. M. and F. R. Thompson. 1997. Forest bird response to regeneration practices in central hardwood forests. Journal of Wildlife Management 61:159-171.
Brewer, R. 1955. Size of home range in eight bird species in a southern Illinois swamp- thicket. Wilson Bull. 67:140-141.
Brown, B. T. and M. W. Trosset. 1989. Nesting-Habitat relationships of riparian birds along the Colorado River in Grand Canyon, Arizona [USA]. Southwestern Naturalist 34:260-270.
Burhans, Dirk E. and Frank R. Thompson. 1999. Habitat patch size and nesting success of yellow-breasted chats. Wilson Bulletin 111. June,:210-215.
Dennis, J. V. 1958. Some aspects of the breeding ecology of the yellow-breasted chat (Icteria virens). Bird-Banding 29:169-183.
DeSante, D. F., and D. G. Ainley. 1980. The avifauna of the South Farallon Islands, California. Studies in Avian Biol. No. 4. Cooper Ornithol. Soc., Lawrence, KA. 104pp.
Dickson, J. G., R. N. Conner and J. H. Williamson. 1993. Breeding bird community changes in a developing pine plantation. Bird Populations 1:28-35.
Ehrlich, P. R., D. S. Dobkin, and D. Wheye. 1988. The birder's handbook. Simon and Schuster, New York. 785pp.
Gaines, D. 1974. A new look at the nesting riparian avifauna of the Sacramento Valley, California. West. Birds 5:61-80.
Gaines, D. 1977. Birds of the Yosemite Sierra. California Syllabus, Oakland. 153pp.
Garrett, K. and J. Dunn. 1981. Birds of Southern California: Status and Distribution. Los Angeles Audubon Society. 407 pp.
Grinnell, J. and A.H. Miller. 1944. The Distribution of the Birds of California. Pacific Coast Avifauna Number 27. Copper Ornithological Club, Berkeley, California. Reprinted by Artemisia Press, Lee Vining, California; April 1986. 617 pp.
Harrison, C. 1978. A field guide to the nests, eggs and nestlings of North American birds. W. Collins Sons and Co., Cleveland, OH. 416pp.
McCaskie, G., P. De Benedictis, R. Erickson, and J. Morlan. 1979. Birds of northern California, an annotated field list. 2nd ed. Golden Gate Audubon Soc., Berkeley. 84pp.
Patten, Michael. 1998. Pers. Comm. Riverside County Editor for American Field Notes and Past Secretary, California Bird Records Committee.
Remsen, J. V., Jr. 1978. Bird species of special concern in California. Calif. Dept. of Fish and Game, Sacramento. Wildl. Manage. Admin. Rep. No. 78-1. 54pp.
Schadd, C.A. and G. Ritchison. 1998. Provisioning of nestlings by male and female yellow-breasted chats. Wilson Bulletin 110:398-402.
Sedgwick, J. A. and F. L. Knopf. 1987. Breeding bird response to cattle grazing of a cottonwood bottomland. Journal of Wildlife Management 51:230-237.
Skagen, S. K., C. P. Melcher, W. H. Howe and F. L. Knopf. 1998. Comparative use of riparian corridors and oases by migrating birds in southeast Arizona. Conservation Biology 12:896-909.
Thompson, C. F., and V. Nolan, Jr. 1973. Population biology of the yellow-breasted chat (Icteria virens L.) in southern Indiana. Ecol. Monogr. 43:145-171.
USFWS. 1999. Unpublished data.
Zeiner, D. C., W., F. Laudenslayer, Jr., K. E. Mayer, M. White. Editors. 1990. California's Wildlife. Volume 2. Birds. State of California, Department of Fish and Game. Sacramento, California. 731 pp.
yellow warbler (Dendroica petechia brewsteri)
SPECIES NAME AND GROUP DESIGNATION
Common Name and Scientific Name:
yellow warbler (Dendroica petechia brewsteri)
Status:
State: Species of Special Concern
Federal: Partners in Flight Priority Bird Species; San Bernardino National Forest Sensitive
Other: Audubon Society Special Concern
GROUP DESIGNATION AND RATIONALE
Group 2
The yellow warbler is relatively well distributed throughout the MSHCP Plan Area within suitable Habitat. There appear to be several Core Areas including the Prado Basin/Santa Ana River, Temescal Canyon and its tributaries, Wasson Canyon, Temecula Creek, Murrieta Creek, Vail Lake area, Wilson Creek, San Timoteo Creek, Santa Rosa Plateau, and drainages and woodland areas within the San Bernardino National Forest. Because Habitat characteristics of the yellow warbler are well known to include riparian scrub and forest and woodland and the yellow warbler occurs in all Bioregions of the Plan Area, but has specific locations that are core areas, the yellow warbler is classified as a Group 2 species and will be managed on a landscape level with site specific requirements.
SPECIES CONSERVATION OBJECTIVES
The species-specific conservation objectives developed for this species are based upon the best available scientific information at the time of MSHCP preparation. Pursuant to Section 5.0 which includes Management, Monitoring and the Adaptive Management Program, the MSHCP's mitigation requirements will be monitored and analyzed to determine if they are producing the desired result. Based upon this information, the following species-specific conservation objectives will be adjusted if appropriate, as new information is gathered during Plan implementation. The Adaptive Management Program will be used to identify alternative strategies for meeting the MSHCP's general biological goals and objectives and, if necessary, adjusting future conservation strategies according to the information received.
Objective 1
Include within the MSHCP Conservation Area at least 34,080 acres of suitable nesting and foraging Habitat for the yellow warbler including riparian scrub, woodland, and forest and oak woodland and forest.
Objective 2
Include within the MSHCP Conservation Area at least 9 Core Areas including Prado Basin/Santa Ana River (9,670 acres), Temescal Canyon including tributaries such as Alberhill Creek (estimated as Subunit 3 of Temescal Canyon Area Plan plus Proposed Constrained Linkage 6 and Proposed Linkage 2; 4,290 acres), Wasson Canyon (Subunit 5 of Elsinore Area Plan; 2,320 acres) Temecula Creek (Subunit 2 of Southwest Area Plan; 850 acres), Murrieta Creek (Subunit 1 of Southwest Area Plan; 2,060 acres), Vail Lake (Subunit 3 of Southwest Area Plan; 12,320 acres), Wilson Creek (Subunit 2 of REMAP Area Plan; 33,540 acres), San Timoteo Creek (Subunit 3 of The Pass Area Plan; 2,290 acres), and drainages and woodland areas within the San Bernardino National Forest (13,720 acres).
Objective 3
Within the MSHCP Conservation Area, maintain (once every 5 years) the continued use of, and successful reproduction at 75 percent of the Core Areas (including any Core Areas identified in the MSHCP Conservation Area in the future). Successful reproduction is defined as a nest which fledged at least one known young.
SPECIES CONSERVATION ANALYSIS
Conservation Levels
For the purpose of the conservation analysis, potential Habitat for the yellow warbler includes riparian scrub, woodland, and forest and oak woodland and forest Habitats for breeding, wintering, and migration stopovers. Based on these Habitats, the Plan Area supports approximately 46,790 acres of potential Habitat for the yellow warbler. Table 1 shows the conservation and loss of potential Habitat for the yellow warbler. Overall, approximately 34,080 acres (73 percent) of potential Habitat in the Plan Area will be conserved in Criteria Area or existing Public/Quasi-Public lands. It is assumed that these lands will be managed for wildlife resources including the yellow warbler.
TABLE 1
SUMMARY OF HABITAT CONSERVATION
YELLOW WARBLER
| Vegetation Type | MSHCP Plan Area (Acres) |
Within MSHCP conservation Area | Outside MSHCP conservation Area | ||||
|---|---|---|---|---|---|---|---|
| Criteria Area1 (Acres) |
Public/ Quasi-Public (Acres) |
Total Within MSHCP Conservation Area (Acres) |
Rural/ Mountainous (Acres) |
Outside MSHCP Conservation Area (Acres) |
Total Outside MSHCP Conservation Area (Acres) |
||
| All Bioregions | |||||||
| Riparian Scrub, Woodland, Forest | 14,610 | 3,920 | 7,270 | 11,190 | 370 | 3,050 | 3,420 |
| Oak Woodlands and Forest | 32,180 | 2,390 | 20,500 | 22,890 | 5,020 | 4,270 | 9,290 |
| TOTAL | 46,790 | 6,310 (13%) |
27,770 (59%) |
34,080 (73%) |
5,390 (12%) |
7,320 (16%) |
12,710 (27%) |
| 1 Acres refer to Additional Reserve Lands to be assembled from within the Criteria Area. | |||||||
This species occurs within the Forest Service lands as well as the lowland Bioregions as a breeding and foraging species. It occurs predominantly within riparian scrub, woodland, and forest. Under the existing Forest Land allocation plan, these locations and Habitats generally are located within the San Jacinto Wilderness area and in most of the grazing allotments. The yellow warbler has been documented to have a core population area within drainages of the San Bernardino National Forest within the western escarpment of the San Jacinto Mountains. It also likely occurs within the Cleveland National Forest, based on the presence of suitable Habitat, although locations have not been documented most likely due to low survey effort or lack of reporting. Conservation of riparian and woodland Habitats within the western escarpment of the San Jacinto Mountains will be important for this species.
In addition, the Riparian/Riverine Areas and Vernal Pools policy described in Section 6.1.2, MSHCP Volume 1, provides for conservation of wetlands which provide Habitat for this species through avoidance and minimization. Mitigation for impacts to wetlands shall be incorporated in accordance with the "No Net Loss" policy of federal and state wetland regulations. The proposed mitigation shall be directly related to the functions and values of the wetland as related to this species and result in equivalent replacement.
As described above under Data Characterization, 47 of the 85 relatively recent point localities have a high location precision. Of these 47 point localities, 8 (17 percent) will be inside the Criteria Area and 12 (26 percent) will be located within Public/Quasi-Public Lands. A total of 4 point locations (9 percent) will be in the Rural/Mountainous zone. Conservation of this species will be considered from a landscape perspective because suitable Habitat characteristics have has been well defined and provision of additional suitable Habitat that is not currently occupied may assist with the recovery of the species.
In addition, there are definable locations of Core Areas for focusing conservation efforts that are included within the MSHCP Conservation area. These include Prado Basin/Santa Ana River (9,670 acres), Temescal Canyon including tributaries such as Alberhill Creek (estimated as subunit 3 of Temescal Canyon Area Plan plus Proposed Constrained Linkage 6 and Proposed Linkage 2; 4,290 acres), Wasson Canyon (Subunit 5 of Elsinore Area Plan; 2,320 acres) Temecula Creek (Subunit 2 of Southwest Area Plan; 850 acres), Murrieta Creek (Subunit 1 of Southwest Area Plan; 2,060 acres), Vail Lake (Subunit 3 of Southwest Area Plan; 12,320 acres), Wilson Creek (Subunit 2 of REMAP Area Plan; 33,540 acres), San Timoteo Creek (Subunit 3 of The Pass Area Plan; 2,290 acres), and drainages and woodland areas within the San Bernardino National Forest (13,720 acres). A total of 81,060 acres of Core Areas are included within the MSHCP Conservation Area. Other known occupied areas within the MSHCP Conservation Area include Potrero Creek, Lake Perris/Mystic Lake, Lake Skinner, and Bautista Creek.
Rural/Mountainous Designation Areas
As depicted on the MSHCP Plan Map (Figure 3-1, MSHCP Volume 1), certain areas adjacent to the MSHCP Conservation Area are designated as Rural/Mountainous in the County's General Plan. These areas are generally constrained for development due to steep topography and the level of development in these areas is anticipated to be of a low density, rural residential character. While these areas will not be included within the MSHCP Conservation Area, managed for the benefit of species conserved under the MSHCP, and the existing zoning/ordinances for these areas do not preclude development and could allow substantial fragmentation and/or degradation of Habitat for proposed covered species, the low levels of development anticipated in these areas may provide an edge to the MSHCP Conservation Area with possible value to certain species. For the yellow warbler, conservation of the Santa Rosa Plateau is important as a Core Area. MSHCP Conservation Area locations in this area are generally surrounded by Rural/Mountainous designations. Potential development in this area is anticipated to retain vacant areas and wetlands, which may provide nesting and foraging Habitat for the yellow warbler. A total of 5,390 acres (12 percent) of potential Habitat will be designated Rural/Mountainous.
MSHCP Conservation Area Configuration Issues
Several large blocks of Habitat supporting or potentially supporting the yellow warbler for breeding, wintering and migration will be conserved as Criteria Area and Public/Quasi-Public designations. Core areas conserved within the MSHCP Conservation Area that are conserved as large blocks of Habitat include the Prado Basin/Santa Ana River, Temescal Canyon including tributaries such as Alberhill Creek, Wasson Canyon, Temecula Creek, Murrieta Creek, Vail Lake, Wilson Creek, San Timoteo Creek, and drainages and woodland areas within the San Bernardino National Forest. Other large blocks of Habitat that are included in the MSHCP Conservation Area include Santa Rosa Plateau Nature Reserve, Lake Skinner-Diamond Valley Lake, Lake Mathews-Estelle Mountain, Lake Perris/Mystic Lake, Sycamore Canyon Regional Park, the Badlands, Kabian Park, upper reach of San Jacinto River, Potrero Valley, and forest service lands within Cleveland National Forest and San Bernardino National Forest. Some of the large blocks of Habitat have not been mapped as containing yellow warblers or drainages with riparian Habitat either due to the small size of the patch of Habitat, lack of suitable Habitat, lack of survey effort, or lack of occupation by the yellow warbler. Typically, these Habitat blocks have smaller riparian systems that contain potential suitable Habitat, which could be occupied by yellow warblers presently or in the future. As a long-distance migrant, yellow warblers are likely able to discover and use patches of riparian Habitat that may not have been used in the past. As such, the MSHCP Conservation Area will include smaller drainages that may support small numbers of the species. The MSHCP Conservation Area will also provide adequate Habitat linkages between Core Areas for this species. The Prado Basin Core Area is linked along the Santa Ana River to San Bernardino and Orange counties. This riparian area is linked to the south by the Temescal Wash to Lake Mathews and Lake Elsinore. Riparian Habitat within the Vail Lake area is linked to the Lake Skinner-Diamond Valley Lake area via Tucalota Creek. The Vail Lake area is also linked to the Santa Rosa Plateau and then to the Santa Margarita River by the riparian Habitat in Temecula Creek and Murrieta Creek. The Badlands area provides a major Habitat block that provides a linkage to Potrero Creek, Lake Perris/Mystic Lake, and San Jacinto Wildlife Area.
Conservation Summary
In summary, conservation for this species will be achieved by inclusion of at least 34,080 acres of suitable Conserved Habitat. Nine of the ten core populations will be conserved in the MSHCP Conservation Area. Conservation of the small patches of riparian Habitat and the sites containing small numbers of yellow warblers may contribute to the populations within the Plan Area. These small populations, documented above to be largely preserved are important to prevent further isolation of remaining core breeding groups. In addition, Objective 3 for this species will maintain (once every 5 years) the continued use of, and successful reproduction at 75 percent of the Core Areas (including any Core Areas identified in the MSHCP Conservation Area in the future). Successful reproduction is defined as a nest which fledged at least one known young.
INCIDENTAL TAKE
The Incidental Take of the yellow warbler is difficult to quantify due to our limited knowledge of its distribution and abundance within the Plan Area. The maximum level of Incidental Take of yellow warblers can be anticipated by the loss of the number of acres of potential Habitat that will become unsuitable for this species. About 12,710 acres (27 percent) of potential Habitat for the yellow warbler will be outside the Criteria Area or Public/Quasi-Public designations, and individuals within these areas will be subject to Incidental Take consistent with the Plan. Of this, approximately 5,390 acres (12 percent) of potential Habitat will be located within areas designated as Rural/Mountainous. While the Rural/Mountainous areas are not included within the MSHCP Conservation Area, will not be managed for the benefit of wildlife, and the existing zoning/ordinances for these areas do not preclude development and could allow substantial fragmentation and/or degradation of Habitat for proposed covered species, the anticipated levels of development in these areas may be consistent with maintaining some Habitat for the yellow warbler. The Core Area within the Santa Rosa Plateau will be outside the MSHCP Conservation Area and individuals within this area will be subject to Incidental Take consistent with the Plan.
SPECIES ACCOUNT
Data Characterization
Data reviewed includes the University of California, Riverside, GIS data base, the California Natural Diversity Data Base (CNDDB), and available literature.
The UCR location database includes approximately 120 location records for the yellow warbler dating from 1900 to 1999. Approximately 85 of these records are relatively recent (dated from 1990 or later) and of these records, approximately 47 are of high precision and may be accurately placed within the Plan Area and are suitable for analysis. The Habitat types with which these data records are associated vary from riparian and woodlands to upland Habitats to residential development and crop lands, thus they likely are occupying small patches of riparian Habitat that have not been mapped within the Plan Area.
The available literature is low to moderate and provides baseline natural history information and Habitat relationship analyses. Few controlled scientific studies have been conducted. Most of the information is provided within the general ornithological literature.
Habitat and Habitat Associations
In general, the yellow warbler breeds most commonly in wet, deciduous thickets, especially those dominated by willows and in disturbed and early successional Habitats (Lowther et al. 1999). At the northern limits of its distribution in northern Manitoba, it occurs in willow scrub near rivers, streams, or lakes. Michigan breeding Habitats include shrub wetland, shrub uplands, old fields, blueberry bogs, semi-open wet deciduous forest, and gardens.
Yellow warblers in southern California breed in lowland and foothill riparian woodlands dominated by cottonwoods, alders, or willows and other small trees and shrubs typical of low, open-canopy riparian woodland (Garrett and Dunn 1981). The yellow warbler is found at elevations from 100 meters to 2,700 meters within riparian Habitat and at higher elevations along watercourses with riparian growth (Lowther et al. 1999).
During migration, they occur in lowland and foothill woodland Habitats such as desert oases, riparian woodlands, oak woodlands, mixed deciduous-coniferous woodlands, suburban and urban gardens and parks, groves of exotic trees, farmyard windbreaks, and orchards (Small 1994). The yellow warbler also breeds in montane chaparral, open ponderosa pine and mixed conifer Habitats with substantial amounts of brush (Zeiner, et al. 1990). Breeding in montane shrubs and conifers is perhaps a recent phenomenon (Gaines 1977). In migration, it visits woodland, forest, and shrub Habitats. It usually arrives in California in April, and generally has migrated out of the area by October. Apparently there is a post-breeding, upslope movement mostly to middle elevations (Beedy 1975); it is scarce at elevations above 2,500 meters (8000 feet) (Gaines 1977). Small numbers regularly overwinter in southern California lowlands (Garrett and Dunn 1981).
Biogeography
Yellow warblers as a whole nest from northern Alaska eastward to Newfoundland and southward to northern Baja California and Georgia. The species migrates throughout much of North America and winters from southern California, Arizona and the Gulf Coast southward to central South America (AOU 1998).
Zeiner, et al. (1990) summarizes the distribution, abundance, and seasonality in California as follows. The yellow warbler is an uncommon to common, summer resident in the north; and locally common in the south. It breeds in riparian woodlands southward from the northern border of the state generally west of the Sierra Nevada to the coastal slopes of southern California and from coastal and desert lowlands up to 2,500 meters (8,000 feet) in the Sierra Nevada and other montane chaparral and forest Habitats (Grinnell and Miller 1944).
The yellow warbler occurs as a migrant throughout the state and there is at least one apparent winter record (Grinnell and Miller 1944). It is a common migrant on the Channel and Farallon Islands in spring and fall (DeSante and Ainley 1980, Garrett and Dunn 1981).
The patterns of population density have probably been in flux since European settlement of North America altered the original vegetation. There are no large-scale range-wide changes that have been documented for the yellow warbler. Populations in the southwestern United States have declined dramatically in recent decades in many lowland areas (southern coast, Colorado River, San Joaquin and Sacramento valleys) (Lowther et al. 1999). It is now rare to uncommon in many lowland areas where formerly it was common (McCaskie, et al. 1979, Garrett and Dunn 1981).
Known Populations Within Western Riverside County
Although the species has certainly declined within the Plan Area in the recent past (Garrett and Dunn 1981), the yellow warbler apparently continues to breed in scattered areas throughout much of western Riverside County in appropriate woodland Habitats. Locations in the northern portion of the Plan Area are widely scattered along the Santa Ana River. The species is also widely scattered along the Interstate 15 corridor from the north to south and then along the southern portion from the Santa Rosa Plateau to Aguanga. Other locations are very widely scattered within the Plan Area in the mountain Bioregions, the northeastern portions of the Plan Area and in the lowlands areas. Significant breeding populations remain in the Prado Basin (Hays, 1999, pers. obs.). Other Core Areas include Temescal Canyon and its tributaries, Wasson Canyon, Temecula Creek, Murrieta Creek, Vail Lake area, Wilson Creek, San Timoteo Creek, Santa Rosa Plateau, and drainages and woodland areas within the San Bernardino National Forest.
Other geographic locations recorded in the UCR database include Pechanga Creek, along the western escarpment of the San Jacinto mountains (Michael Patten, Riverside County Editor for American Field Notes and Past Secretary, California Bird Records Committee, pers. comm., 1998), Potrero Creek, Lake Perris/Mystic Lake, Lake Skinner, Bautista Creek, and Motte Rimrock Reserve.
Biology
Genetics: Classification of the broad range of morphological variation in the yellow warbler has ranged from recognizing several species to one highly polytypic species often divided into three groups that reflect nomenclatural history (Lowther et al. 1999). The current taxonomy defines three groups of subspecies with each group at times having been regarded as a distinct species. The geographic variation in plumage is rather marked between the groups, but is subtle and clinal within the groups. Morphometric analysis over the range of the species shows a general trend toward larger size from north to south.
Studies of mtDNA revealed moderately high genetic differentiation within the species with estimated sequence divergence of 0.14 percent to 3.17 percent among all groups. The geographic pattern of haplotypes found in this study suggests multiple colonization responsible for the current distribution (Lowther et al. 1999).
Diet and Foraging: The yellow warbler forages for insects and spiders in the upper canopy of deciduous trees and shrubs. Occasionally it hawks insects from air, or eats berries. It gleans and hovers in the upper canopy of deciduous trees and shrubs. (Bent 1953, Ehrlich, et al. 1988). Summer observations of foraging showed that small limbs are preferred to large limbs, tips, and dead limbs for both deciduous and coniferous trees (Morse 1973). Foraging is typically observed between 1 to 55 feet (0.3 to 16.8 meters), at the top of the vegetation, never on the ground and mostly between 6 to 8 meters.
Daily Activity: The yellow warbler exhibits year-long, diurnal activity. It is a nocturnal migrant (Zeiner, et al. 1990).
Reproduction: The preferred nest trees are willows, alders, and cottonwoods. Yellow warblers have been identified using a tamarisk (Tamarix ramosissima) community at Glen Canyon Dam where creation of this Habitat mimics native Habitat and enhanced breeding Habitat for this and ten other species (Brown and Trosset 1989). The nest is an open cup placed 0.6 to 5 meters (2-16 feet) above ground in a deciduous sapling or shrub. It breeds from mid-April into early August with peak activity in June. The pair breeds solitarily. It lays 3-6 eggs (usually 4 or 5); eggs are incubated by the female for 11 days. The altricial young are tended by both parents until fledging at 9-12 days (Harrison 1978). The young breed the following year. The territory often includes tall trees for singing and foraging and a heavy brush understory for nesting (Ficken and Ficken 1966).
Survival: Nest predation was found to be the major cause of nest failure in a group of species in Alaskan wetlands including yellow warblers (Rodgers 1995). The annual adult survival rate, based on returns of banded birds to the same breeding location is 0.526. The maximum reported longevity is 8 years, 11 months by a male yellow warbler (Klimkiewicz, et al. 1983).
Dispersal: No available information.
Socio-Spatial Behavior: On the breeding grounds, the yellow warbler defends multipurpose territories. The territory interactions are dynamic and continue throughout the breeding season. Territories are established as soon as the males arrive (Lowther et al. 1999). The species tends to have relatively small territories and home ranges, varying from 0.08 to 0.5 acre (Ficken and Ficken 1966, Beer, et al. 1956). Peak densities measured in southeast Arizona reached 48 birds per hectare (Skagen, et al. 1998). The home range was recorded as less than 0.2 hectares (0.5 acres) in New York (Ficken and Ficken 1966), and 0.16 hectares (0.4 acres) in lowa (Kendeigh 1941a). Kendeigh observed individuals regularly moving up to 488 meters (1,600 feet) to a willow-marsh edge to feed. The territory varied from 0.03 hectares (0.08 acres) on small islands in Minnesota (Beer, et al. 1956), to 0.36 hectares (0.9 acres) in a swamp thicket in Illinois.
Community Relationships: The yellow warbler is subject to predation by small mammals, accipiters, corvids, and snakes. The species is susceptible to brood parasitism by brown-headed cowbirds. Brood parasitism by brown-headed cowbirds is heavy and apparently has been a major cause of the drastic decline in numbers in lowland localities in recent decades (Bent 1953, Garrett and Dunn 1981, Remsen 1978). Parasitism occurred in 9 of 25 nests or family groups in the Sierra Nevada where cowbirds were common (Rothstein, et al. 1980, Verner and Ritter 1983, Airola 1986). The yellow warbler frequently responds to cowbird parasitism by building over the parasitized clutch making multi-tiered nests. The yellow warbler is more likely to desert or bury the cowbird egg if the cowbird egg appears before any warbler egg or appear early in the laying sequence (Lowther et al. 1999).
Threats to Species
Major continuing threats to the species include Habitat destruction and fragmentation and brood-parasitism by brown-headed cowbirds (Molothrus ater) (Garrett and Dunn 1981). The populations in the western United States are affected by intense grazing especially where willow growth along riparian Habitats is reduced or removed. The subspecies of this species, D. p. sonorana, which formerly bred along the length of the Colorado River, may have been completely extirpated from California (Garrett and Dunn 1981).
Special Biological Considerations
This species has increased dramatically within the Prado Basin during the course of 14 years of cowbird management and Habitat conservation efforts there (Hays, 1999, pers. obs.). The number of breeding territories has increased from approximately 5 in 1986 to over 250 in 1998 (Hays, 1986, pers. obs.; James Pike, 1998, USFWS, pers. comm.).
In a study in Oregon on the effects of cattle grazing on riparian Habitat, a negative correlation was found between shrub volume and the frequency of cattle use (Taylor and Littlefield 1986). A positive correlation was found between the time since a transect was last grazed by cattle and shrub volume. Photographic evidence substantiated the improvement in riparian vegetation when protected from cattle in this study. Yellow warblers were more numerous on transects with abundant willow and little or no cattle than on transects with heavy cattle use and low shrub volume. The yellow warbler population increases coincide with a dramatic decrease in cattle on the refuge and the elimination of willow cutting and spraying. The transect data show that the high numbers of the species are correlated with the amounts of healthy willows which are used for nesting sites.
A study of stopover sites in southeastern Arizona led researchers to conclude that riparian patches are important as stopover sites for migrants regardless of size and degree of isolation or connectivity (Skagen, et al. 1998). Other researchers in Oregon specifically identified "mesic shrub vegetation" as a vegetation structure within riparian areas which provides high species richness and abundance including high numbers of yellow warblers (Sanders and Edge 1998).
The yellow warbler appears to select the nest site based on the patch within which the nest tree or shrub is located (Knopf and Sedgwick 1992). The best predictor of nest site selection is based on the patterning of horizontal structure. The yellow warbler seems to select nest sites based upon patch characteristics surrounding the nest site. This may help reduce predation or nest parasitism. The yellow warbler thus seems to prefer to select a nest site in a larger stand of vegetation with intermingling branches rather than isolated shrubs (Knopf and Sedgwick 1992).
Parental care investment by the yellow warbler varies among individuals. The female of the pair is apparently able to assess the potential contribution of the male prior to mating (Lozano and Lemon 1996). If the male does not contribute sufficiently to the parental care of the young, the female will make up for it but will do so at the cost of a reduced growth rate of the young. In an insect rich environment, the male may attempt to mate with a second female and reduce his parental investment but increase his overall fitness by producing a second clutch. The young of the first mated female may suffer from predation or be less able to survive due to the lack of the males parental care (Lozano and Lemon 1996). The lower amount of parental investment of the male may be related to the high quality of the territory that he occupies which is reflected in the large amount of shrubs surrounding the nest site. The success of the male's selection of the higher quality territories may be related to the larger amount of brown striping on the breast plumage of the male (Studd and Robertson, 1989; Studd and Robertson 1988).
LITERATURE CITED
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