Sonoran Desertscrub
1. Habitat Description, Status and Importance
Arizona contains more Sonoran Desertscrub habitat than any other state in North America, putting Arizona in a position of great responsibility for protecting and maintaining this habitat. This unique ecosystem is home to many Sonoran Desertscrub obligate species. Although few species are in immediate danger of extirpation and only one bird species made "priority status," the continued population growth and urban expansion in Arizona pose real and immediate threats to many of the obligate species. This section is organized differently than other sections of the plan to better identify the importance of Sonoran Desertscrub to Arizona’s bird species. We will address some of the currently known threats and identify those bird species that may be directly affected by them in the near future. The term desert and desertscrub are used interchangeably here and have the same meaning.
The Sonoran Desertscrub habitat is located in the region immediately surrounding the Gulf of California in the extreme southwestern portion of the United States. It occurs in southwestern Arizona, southeastern California, most of Baja, California and the western half of the State of Sonora, Mexico. In Arizona, the Sonoran Desertscrub encompasses 40,540 square miles (10,499,850 ha; 25,945,600 ac) (Shreve and Wiggins 1964); which accounts for approximately 34% of the total habitat range. Only Sonora, Mexico has a larger percentage (41%) of Sonoran Desertscrub habitat.
Sonoran Desertscrub habitat is characterized by low and unevenly distributed rainfall that ranges from 0-13 inches per year. In Arizona, summer and winter are the primary precipitation periods, with the majority of precipitation falling in the summer (Brown 1982). Other common characteristics include low humidity, high air temperatures with great daily and seasonal ranges, soil with low organic content and high mineral salt content, and sporadic stream flow (Shreve and Wiggins 1964).
The Sonoran Desertscrub habitat lies below 915 m (3000 ft) except for the narrow band along the eastern edge of Arizona which reaches 1050 m (3450 ft). Vegetation within this biome differs from the other deserts by the greater presence of tree species, truly large cacti and succulent constituents. The Sonoran Desertscrub exceeds the Mohave, Chihuahuan, Great Basin deserts in number and variety of life forms and diversity of plant communities.
Brown (1982) divided the Sonoran Desertscrub habitat into five subdivisions but only two, the Lower Colorado River Valley and the Arizona Upland occur in Arizona. The following are descriptions of the plant communities found within these two Arizona subdivisions.
a. Lower Colorado River Valley Subdivision is the largest and most arid subdivision of the Sonoran Desert, and is dominated by two communities; creosotebush-white bursage and saltbush. The creosotebush-white bursage series occurs over broad valleys and decreases in importance as the slope increases (such as on bajadas or sloping plains). The dominant plants (as expected) are creosotebush and white bursage. Other plant species include big galleta, indigo bush, longleaf ephedra and desert buckwheat.
Before cultivation, the saltbush series was the most widespread community in the Gila Valley, Arizona (Brown 1982). The soil is finer and water retention capacity greater than the creosote-white bursage series (Brown 1982). The saltbush series is found on gently sloping lands. Common plants found within this community include all-scale, narrow leaved wingscale, lycium, globe mallow species, burrowweed, and creosotebush.
In addition to the preceding communities, the Lower Colorado River Valley subdivision also includes the following communities: creosotebush-big galleta and mixed scrub series. As the name implies, the creosotebush-big galleta series is dominated by creosotebush and the big galleta, a shrub-like grass. This series occurs primarily on sandy plains or dune situations. The mixed scrub series occurs along washes and provides for a more diverse array of vegetation due to the increased moisture regime. This series intergrades within other series especially the creosote-white bursage series. The primary vegetation has greater structural diversity, characterized by blue paloverde, ironwood, smoketree as well as shrubs like desert lavender, jojoba and indigo bush.
Bird species typical of Lower Colorado River Valley Subdivision are: Le Conte’s Thrasher, Black-throated Sparrow, Verdin, Loggerhead Shrike, Lesser Nighthawk and Black-tailed Gnatcatcher.
b. Arizona Upland Subdivision represents some of the most commonly recognized habitat in the Sonoran Desert. More than 90% of this Subdivision occurs on slopes, broken ground and multi-dissected sloping plains (Brown 1982). It is dominated by tree species that were confined to drainages in the Lower Colorado River Valley Subdivisions as well as an abundance of cacti species. This community is noted for its rich diversity of bird species (Brown 1982). There are three communities within the Arizona Upland Subdivision; paloverde-cacti-mixed scrub, creosotebush-crucifixion thorn, and jojoba-mixed scrub. The paloverde-cacti-mixed scrub series is the most extensive of the three series (Brown 1982). Dominant plant species within this series include; little-leaf paloverde, blue paloverde, saguaro, mesquite, ironwood, desert hackberry, whitethorn acacia, ocotillo, triangle-leaf bursage, little-leaved rattany, and prickly pear, pincushion, hedgehog, and barrel cacti.
The jojoba-mixed scrub series is best developed in the transition zone between Sonoran Desertscrub and interior chaparral (Brown 1978). Because its distribution is almost completely within the Sonoran Desert (Hastings and others 1972) it is included as a Sonoran Desertscrub series regardless of its "chaparral-like" physiognomy. This series is dominated by the jojoba plant.
The creosotebush-crucifixion thorn series is particularly common on limestone substrates at the northern and eastern edges of the Sonoran Desert (Brown 1982). This series can intergrade into semi-desert grassland habitat. The dominant plant species are crucifixion thorn, creosotebush and acacia species.
Bird species typical of the Arizona Upland Subdivision are: Harris Hawk, White-winged Dove, Roadrunner, Mourning Dove, Verdin, Cactus Wren, Black-tailed Gnatcatcher, Phainopepla, Gambel's Quail, Costa's Hummingbird, Gilded Flicker and Gila Woodpecker.
2. Current Threats to Sonoran Desertscrub Habitat and Sonoran Desert Dependant Birds
Impacts of Growing Urbanization on Sonoran Desertscrub Nesting Birds
Conversion to urbanized landscapes is an increasing threat to the Arizona Upland subdivision of Sonoran Desert Scrub. Population growth in Arizona, especially Maricopa and Pima counties, has been dramatic. Between 1980 and 1996, Arizona grew by 64.3 percent. During this period, the population in Pima County increased by 46.9 percent. This growth is expected to continue with the population in Pima County projected to increase to 854,330 by the year 2000, to exceed 1 million by the year 2009, and to double by the year 2050 (Pima Association of Governments 1997).
The resulting conversion of native vegetation to housing and business developments may affect some bird species more than others. Those bird species that are sensitive to urbanization should be tracked for several reasons: 1) the current rates of urbanization are great, 2) these species may become rare in the future if conversion of desert scrub to urban development continues at the present rate, and 3) responses of these species to development may provide an indication of how well attempts to minimize the impacts of urban development are working.
Overall, bird species sensitive to urbanization include cavity nesters, insectivores, ground nesting species, and many species that feed on the ground or in low shrubs (Beissinger and Osborne 1982). In Arizona, Black-throated Sparrows and Black-tailed Gnatcatchers, in particular, are associated with undisturbed native vegetation (Germaine 1995). These two species do not occur in even low density housing developments, and have been found sensitive to urbanization by every study in Tucson (Emlen 1974, Frederick 1996, Germaine 1995, Mills and others 1989, Stenberg 1988, Tweit and Tweit 1986). We should monitor these two species in urbanizing areas. Several other species have been found sensitive to urbanization in one or more of the following studies: Emlen (1974), Tweit and Tweit (1986), Mills and others (1989), Stenberg (1988), Germaine (1995), and Frederick (1996). These include Northern Flicker, Pyrrholoxia, Verdin, Gambel’s Quail, Ash-throated Flycatcher, Greater Roadrunner, Rufous-winged Sparrow, and Ladder-backed Woodpecker. They also occur more frequently in natural open spaces than other land use types along the river corridors of Tucson (except Gambel’s Quail, and including Brown-crested Flycatcher, Abert’s Towhee, Brown Towhee, Black-chinned Hummingbird, and Phainopepla) (Frederick 1996). Four other Sonoran Desert species that should be considered for monitoring include Purple Martin, Le Conte’s Thrasher, Elf Owl, and Lesser Nighthawk. Casual observations suggest these species are less abundant in urban areas. In addition, their natural history characteristics are typical of those birds that are generally sensitive to urbanization.
Impacts of Fire in the Arizona Upland subdivision of the Sonoran Desert
In recent years, impacts of fires in the Sonoran Desert have increased over historic levels (McLaughlin and Bowers 1982, Schmid and Rogers 1988). Prior to widespread anthropogenic impacts, the sparsity of ground cover and the open spacing between shrubs and trees limited the spread of fires that did ignite in the desert via lightning strikes. This historic lack of fires resulted in a plant community in the Sonoran Desert which is not adapted to fire in the same way as some of the other plant communities found in the state, e.g. ponderosa pine forests, chaparral, and grasslands (Narog and others 1995, Thomas 1991). The widespread establishment of red brome and other exotic annuals has increased ground cover in the desert and thus promotes fire spread (Narog and others 1995, Schmid and Rogers 1988). The number of fires has also increased due to increased human caused fires (Schmid and Rogers 1988).
Although specific impacts of fires vary depending on many factors, desert fires do directly kill many plants (Bunting and others 1980, Cave and Patten 1984, McLauglin and Bowers 1982, Rogers 1985, Thomas 1991). There is also evidence to suggest that the increased frequency of fires in the Sonoran Desert may be changing the structure and species composition of some areas. Saguaro, other cacti and some perennial trees and shrubs, such as paloverde and bursage, are frequently killed and slow to recover after a fire, while other species such as catclaw, creosote, and jojoba recover more quickly (Brown and Minnich 1986, McAuliffe 1997, Narog and others 1995, Rogers 1985). This type of disruption can be predicted to impact bird and other wildlife communities (as by loss of nest cavities in saguaros), as well as negatively impacting the aesthetics of this habitat and perhaps causing irreparable damage to this plant community which in many ways typifies Arizona.
Impacts of Grazing on Sonoran Desertscrub Habitat
Grazing in the Sonoran Desert has progressed over the last several hundred years from smaller, somewhat confined areas of intensive grazing to large expanses of intensive grazing (Nabhan and Holdsworth 1998). Years of overstocking on public and private lands have impacted the composition and condition of Sonoran Desertscrub habitat. The effects of grazing on Sonoran Desertscrub habitat will vary from site to site depending on several factors. These include soil type, plant community, rainfall and the intensity and duration of grazing. Removal of herbaceous cover increases runoff and decreases the water-holding capacity of some soils. In general, clayey and sandy soils with few rocks are more susceptible to erosion from both wind and water. Clay/loam upland soils become ineffective users of summer rainfall when the herbaceous cover is removed.
Plant communities are largely determined by soil types. In plant communities where there are low diversity and few forage species, such as the creosote/bursage community, there is little change in vegetation from continuous heavy grazing. However, where a more diverse plant community exists, continuous heavy grazing will result in the removal of palatable species (grasses, forbs and some shrub species) and the subsequent spread of exotic species, usually non-palatable forbs and woody plants. Grazing, regrazing and trampling will damage vegetation and soil. Periods of rest are vital for plants to regenerate; however, desertscrub habitat recovers slowly so habitat may never fully recover from intensive and extensive grazing.
Three types of grazing regimes are authorized on public lands in the Sonoran Desert. Perennial allotments that permit year-long grazing of perennial vegetation at an established stocking rate, stocking of ephemeral allotments which enables the land manager to take advantage of abundant growth of annual plants averaging 3 out of 10 years and perennial-ephemeral allotments which combine these two types.
Impacts of Burro Browsing on Sonoran Desertscrub Habitat
Desert vegetation in some areas, particularly in western Arizona, is subject to heavy browsing by feral burros. Like birds, burros tend to concentrate in desert washes, at least during times of drought or extreme heat. Seegmiller and Ohmart (1981) found that mesquites and paloverdes were among the most important food items of burros along the Bill Williams River and noted the particularly destructive and wasteful methods by which burros feed on paloverdes. In areas along the Colorado River overused by burros, no small paloverde branches remain within their reach. For small trees, this means that only a trunk remains. Such heavy browsing is particularly detrimental for paloverdes because of their poor regenerative abilities.
This long-term damage to desert vegetation may be expected to have direct impacts on birds. The insect abundance associated with trees and shrubs along desert washes is an important source of food for wildlife. Paloverdes, ironwoods, and mesquites in particular appear to harbor large numbers of insects when leaves are present, and even more when flowering. Birds depend upon these resources during the critical times of spring migration and nesting (Mills and others 1991). In addition, birds particularly favor paloverdes for nesting. Of 579 nests analyzed by the Arizona Breeding Bird Atlas project in Sonoran Desert habitat during 1994-1996, 269 (46%) were in washes and 203 (35%) were in paloverdes (ABBA unpubl. data). Of the 269 nests within washes, 139 (52%) were in paloverdes.
Arizona Breeding Bird Atlas data also revealed that birds that nest in paloverde trees commonly do so at heights within the reach of browsing burros. Though the average height of paloverdes that contained a nest was 5.0 m (16.5 ft), the average height of nests was only 2.0 m (6.5 ft), with a median of 1.8 m (6 ft). Burros can reach to at least this height and can pull down branches that extend even higher. Many birds prefer to nest near the outer edges of paloverdes among smaller branches. Mean distance from the trunk for nests in paloverdes was 1.35 m (4.5 ft). We have observed that in areas heavily used by burros, no small branches remain below 2 m (6.5 ft)on any paloverdes. Bird nesting sites are disappearing in these areas and recruitment of young trees for future nesting sites is nonexistent.
3. Species Descriptions, Objectives and Recommendations
The bird species identified in this section do not meet the APIF requirements for "priority" status (except for Cactus Ferruginous Pygmy-Owl), but are described here as indicators of Sonoran Desertscrub habitat health. At the end of the Sonoran Desertscrub habitat section, a table outlines bird species habitat needs in a quick reference format (Table 14).
Cactus Ferruginous Pygmy-Owl (Glaucidium brasilianum cactorum)
Associated Species in Sonoran Desert: Other species that may use similar habitat components or respond positively to management for the Cactus Ferruginous Pygmy-owl are: Harris’s Hawk, Gila Woodpecker, Gilded Flicker, Gambel’s Quail, Curve-billed Thrasher, Black-tailed Gnatcatcher, Phainopepla, Cactus Wren, Verdin, Elf Owl, Pyrrhuloxia, Ash-throated Flycatcher, Abert’s Towhee, Hooded Oriole, and Scott’s Oriole.
Associated Species in Lowland Riparian: Other species that may use similar habitat components or respond positively to management for the Cactus Ferruginous Pygmy-owl are: Lucy’s Warbler, Bell’s Vireo, Brown-crested Flycatcher, Bewick’s Wren, Hooded Oriole, Gila Woodpecker, Yellow Warbler, Yellow-breasted Chat, Yellow-billed Cuckoo, Ladder-backed Woodpecker.
Distribution: The Cactus Ferruginous Pygmy-Owl occurs from lowland central Arizona south through western Mexico to the States of Colima and Michoacan, and from southern Texas south through the Mexican States of Tamaulipas and Nuevo Leon. South of these regions and through Central America, G.b. ridgwayi replaces G.b. cactorum (Fisher 1893a, Friedmann and others 1950, Johnsgard 1988, Karalus and Eckert 1974, Oberholser 1974, Phillips and others 1964, van Rossem 1937, Schaldach 1963, de Schauensee 1966). In Arizona, its range is limited to Sonoran desertscrub and riparian habitats below 1220 m (4000 ft) in elevation in central and southern Arizona.
Ecology: Pygmy-owls are considered non-migratory throughout their range, having been reported during the winter months at Organ Pipe (Johnson unpubl. data 1976, 1980, T. Tibbitts pers. comm. 1997), Rillito Creek near Camp Lowell at present-day Tucson (Bendire 1888), and Sabino Canyon (USFS unpubl. data). Currently, the earliest nesting record in Arizona is from the collection of five eggs on April 12th , recorded in the United States National Museum (USNM 1996). Due to the small population size and secretive nature of Cactus Ferruginous Pygmy-Owls in Arizona, information is limited. However, recent studies in Arizona have documented copulation on March 31, with egg laying estimated to have taken place between April 6 and April 11, 1996. Working backwards from a confirmed fledging event, the latest record of egg laying is estimated to have been between May 31-June 5 in Tucson, Arizona (Abbate and others 1996). Cactus Ferruginous Pygmy-Owls nest in a large cavity in a tree or large columnar cactus. These cavities may be naturally formed (e.g. knotholes) or excavated by woodpeckers. Nest lining material may or may not be used. Cavities are variously lined with nesting materials or left unlined (Abbate and others 1996, Breninger 1898, Proudfoot 1996). Juveniles remain in close proximity to adults until dispersal. While data is limited, studies indicate that juvenile Cactus Ferruginous Pygmy-Owls have dispersed at least four miles in Texas and two miles in Arizona from their natal sites before establishing their own territories (Proudfoot 1996, S. Richardson pers. comm., AGFD 1997).
Habitat Requirements: In Arizona, the Cactus Ferruginous Pygmy-Owl is primarily associated with the Arizona Upland Subdivision of the Sonoran Desert, below (1220 m) 4000 ft in elevation. Generally, vegetation at these sites includes both species and structural diversity, with well-developed ground cover, mid-story, and canopy layers. The density of the vegetation is likely required to provide an adequate prey base for the Cactus Ferruginous Pygmy-Owl, as well as cover from aerial predators. In riparian areas, plant species may include Fremont cottonwood, willow species, hackberry, and mesquite species. Within Sonoran desertscrub, plant species generally include saguaro, mesquite, paloverde, and ironwood. While the Cactus Ferruginous Pygmy-Owl was historically considered to be a riparian species, little is known about its use of standing water. For Cactus Ferruginous Pygmy-Owls occurring in Sonoran desertscrub, only three observations of direct water use by pygmy-owls for drinking or bathing have been documented (Abbate and others 1996). Cactus Ferruginous Pygmy-Owls within the Tucson, Arizona area, as well as some of those at Organ Pipe Cactus National Monument, occur in close proximity to residential developments in low density housing areas not exceeding one house per 3.3-40 acres where those developments occur adjacent to larger, undeveloped tracks of desertscrub habitat (M. Richardson pers. comm., USFWS 1997).
Habitat and/or Population Objectives:
Population Objective
1. Maintain and increase current population in suitable habitat.
Habitat Strategy
1. Protect known breeding locations from disturbance (i.e. recreation, development etc.).
IMPLEMENTATION RECOMMENDATIONS AND OPPORTUNITIES
Management Issues with Conservation Recommendations
The lack of natural history information for this species has made species management difficult. Riparian and Sonoran desertscrub habitat losses are considered a primary factor in the decline of this species, as well as an on-going threat (Abbate and others 1996, Bahre 1991, Brown and others 1977, Rea 1983, Stromberg 1993, Stromberg and others 1992, Szaro 1989, Willard 1912). Current development pressure around major metropolitan areas, such as the city of Tucson, is resulting in on-going habitat losses (Abbate and others 1996, M. Richardson pers. comm., USFWS 1997). Additionally, increased recreational use and an invasion of nonnative grasses in Organ Pipe Cactus National Monument, increases the risk of habitat loss through wildfire (H. Smith in litt. 1996).
Cactus Ferruginous Pygmy-Owl management issues are listed in italics. Below each issue are Arizona Partners in Flight Conservation Recommendations.
Habitat Loss
1. Restore, maintain riparian and high quality saguaro, paloverde, ironwood, mesquite habitats.
Urbanization
1. Incorporate owl habitat needs into regional planning.
2. Encourage native landscaping, especially in areas adjacent to natural open space.
3. Maintain larger tracks of existing native habitat.
Human Disturbance
1. Educate bird enthusiasts and recreationists on possible sensitivity and encourage them to avoid known breeding areas.
Fire
1. Implement full fire suppression in suitable habitat.
2. Reduce fuel loads along roadways to lower risk of fire.
Implementation Opportunities
1. Increase coordination with local government planning.
2. Identify funding sources for research (especially in Mexico).
EVALUATION OF ASSUMPTIONS: RESEARCH AND MONITORING
Recommended Research
1. Increase research in Sonora, Mexico to determine distribution and genetic relationship between the Arizona and the Mexican species.
2. Conduct comprehensive surveys throughout AZ uplands and riparian habitat.
3. Determine the limiting factor in existing riparian habitat.
4. Investigate juvenile dispersal, home breeding range, wintering range, and habitat use by banding and telemetry.
5. Investigate methods to prevent high intensity fires in Sonoran Desert (specifically red brome).
6. Continue to collect natural history information (specifics on prey base).
NOTE
: The remainder of species identified in this Sonoran desertscrub habitat section have NOT been identified as priority species and are currently stable. However, each of them is dependent on Sonoran desertscrub habitat for its survival and may be at risk in the near future as urbanization and to some extent fire, continue to consume this habitat. Since Arizona contains more Sonoran desertscrub habitat than any other state in the nation, we have a high responsibility to the birds dependent on it. The following species are included here as "red flags" for this unique desert habitat.Costa’s Hummingbird (Calypte costae)
Associated Species: Other species that may use similar habitat components or respond positively to management for Costa’s Hummingbird are: Ladder-backed Woodpecker, Curve-billed Thrasher, Ash-throated Flycatcher, Verdin, Black-tailed Gnatcatcher, Cactus Wren, White-winged Dove, Phainopepla, and Scott’s Oriole.
Distribution: The Costa's Hummingbird occurs in most of the lower Sonoran and limited portions of the upper Sonoran life zones of western North America. It is much less common but widespread in the Mohave desertscrub habitat (Baltosser and Scott 1996). Geographically, this translates primarily to western Arizona, southern California and limited portions of Nevada and Utah. In California, Costa’s Hummingbird habitat extends as far north as Santa Barbara County along the coast; inland the northern extension coincides with the Mohave desert range extending east into southern Nevada to the Utah border. The range extends south through the western half of Arizona and into the western half of the States of Sonora and Sinaloa in Mexico. The breeding range extends further south in Baja covering the entire peninsula as well as all the islands in the Gulf of California larger than 30 km2 (Baltosser and Scott 1996). The non-breeding range remains unchanged south of the Mexican border, with the exception of a southward extension along mainland Mexico to the State of Jalisco. North of the border, the wintering range for Costa’s Hummingbird shrinks south and west withdrawing from Nevada and concentrating along the western Arizona border except for pockets around Phoenix and Tucson. Within California, the range shrinks southward along the coast.
Within Arizona, breeding habitat for the Costa’s Hummingbird stays strictly within the Sonoran desertscrub habitat, rarely exceeding 1000 m in elevation. This coincides primarily with southwestern and southcentral Arizona. Breeding occurs in the Mohave desertscrub along the Nevada border and lower Grand Canyon region and a few scattered sites in southeastern part of the State (Baltosser and Scott 1996). Postbreeding range recently reconfirmed to include lower slopes of Huachuca Mountains (S. Williamson and T. Woods in litt.) and the upper San Pedro River (D. Krueper pers. comm.). Wintering range also in Sonoran desertscrub habitat.
Ecology: Most birds arrive in desert in October/November wintering locally in desertscrub habitat; increasing in numbers and range until they reach the peak of breeding activity in March/April (Baltosser and Scott 1996). Most birds leave desert areas by May-June or earlier (Baltosser and Scott 1996, Monson and Phillips 1981). From June through August, limited numbers of Costa’s Hummingbirds can be found in the lower elevations in the mountain foothills. The earliest known nesting date was January 29 (nest with eggs) while the latest evidence was nest building on June 3 (ABBA unpubl. data).
Costa’s Hummingbirds have been recorded nesting predominately in southwestern and southcentral Arizona below 3300 ft. Fewer records have been recorded from the SE quadrant of the State. Nesting has been confirmed north of Phoenix southeast to Tucson. In addition, breeding has been confirmed in isolated locations such as the Grand Canyon and the extreme southeastern corner of the State (near the New Mexico border) (ABBA unpubl. data). No breeding has been recorded in the NE quadrant of the State (ABBA unpubl. data).
Costa’s Hummingbirds typically build nests in a shrub or tree approximately 1-2 m above ground; the support structure can be living or dead and considerable variation occurs among habitat types. In Arizona, the most common nest plant is foothill paloverde, followed by jojoba, blue paloverde, ironwood, canyon ragweed, hopbush and goldenweed (ABBA unpubl. data, Baltosser and Scott 1996). The nest is composed primarily of small pieces of plant material and feathers fastened with spider web (Baltosser and Scott 1996). Plant material can include bark, small leaves, flower bud scales, ball-like flower heads, bits of lichen, dandelion or thistle heads, and other downy material.
Primarily nectar feeders, the two most important plant species for the Costa’s Hummingbird are chuparosa and ocotillo. Chuparosa has a lengthy flowering period and is the most reliable and productive of midwinter nectar sources (Scott 1994). Some populations can flower for 6 months from fall through spring breeding period (Baltosser and Scott 1996, Rea 1983, Weathers 1983). Ocotillo has a much shorter (3-4 week) but predictable flowering season in March/April (Baltosser and Scott 1996, Waser 1979). Other nectar sources include: desert lavender, thornbush (Lycium), creosotebush, fairy duster, foothill paloverde, saguaro, desert willow, ironwood, desert honeysuckle, barestem larkspur and Mojave beardtongue (Baltosser and Scott 1996). Although there is little information, all hummingbirds (including Costa's) supplement their diet with insects presumably to satisfy protein requirements. Female hummingbirds require additional protein during egg-laying and when feeding young (Brice and Grau 1991).
Habitat Requirements: Costa’s Hummingbirds breed primarily in Sonoran desertscrub habitat and within the United States, Arizona has the greatest concentration of desertscrub (Shreve and Wiggins 1964). Only the State of Sonora, Mexico, has a higher percentage of desertscrub habitat. In Arizona, Costa’s Hummingbirds occur along desert washes, bajadas or mesa's. They are extremely xerophilous (adapted to hot, dry environments). Baltosser and Scott (1996) described the following three plant associations where Costa's can be found: 1) dry washes lined with foothill paloverde, blue paloverde, catclaw acacia, ironwood, and smoketree or filled with shrubs such as creosotebush, jojoba, desert lavender and chuparosa; 2) steep rocky slopes with ocotillo and foothill paloverde; 3) gently sloping bajadas covered with saguaro, creosotebush, and cholla cacti. Costa’s Hummingbirds select drier desertscrub even when adjacent to riparian habitat (Brown 1992, Szaro and Jakle 1985). Winter flowering of a few key species such as chuparosa my be crucial, allowing Costa’s Hummingbird to persist with little interference from other hummingbird species (Baltosser and Scott 1996).
IMPLEMENTATION RECOMMENDATIONS AND OPPORTUNITIES
Management Issues with Conservation Recommendations
Population levels for Costa’s Hummingbirds are relatively stable and the bird is still common throughout much of its' range (Baltosser and Scott 1996). However, the Sonoran desertscrub which constitutes the primary habitat for the Costa’s Hummingbird is facing increasing threats from habitat modification (Baltosser and Scott 1996). Urbanization is increasing at an alarming rate and the Costa's appears to have limited adaptive capability to non-native vegetation and hummingbird feeders (Baltosser and Scott 1996). Whether this is due to direct competition with the more aggressive Anna's Hummingbird or other reasons is unknown. Grazing is a second impact to desertscrub habitat. Grazing impacts on the Costa’s Hummingbird are unknown; although some nectar plants are thorny and resistant to grazing, shrub seedlings and herbs can be affected (Baltosser and Scott 1996). Similarly, browsing by feral burros, especially of foothill paloverdes, may greatly reduce Costa’s preferred nesting substrate. Fire is a third element to impact the Costa's habitat. The introduction of non-native grasses into desertscrub habitat has increased fire potential. The desertscrub habitat is not fire-adapted and many tree species used for nesting are impacted. On the other hand some forage species such as chuparosa appear to respond well to fire (Baltosser and Scott 1996). Although current population trends for the Costa’s Hummingbird are stable; the exponential rate of desertscrub habitat conversion raises concerns for the future stability of species dependent upon Sonoran desertscrub habitat.
Costa’s Hummingbird management issues are listed in italics. Below each issue are the Arizona Partners in Flight Conservation Recommendations.
Habitat Loss
1. Encourage maintenance of native vegetation.
2. Encourage landscaping with native vegetation.
3. Discourage unsustainable livestock management practices.
4. Manage burros before habitat is damaged.
5. Encourage fencing to keep feral animals and cattle out of prime costa’s habitat.
Fire
1. Implement full suppression.
2. Reduce fuel loads along roadways.
Implementation Opportunities
1. Plant and maintain more native vegetation, especially tubular flowers.
EVALUATION OF ASSUMPTIONS: RESEARCH AND MONITORING
Recommended Research
1. Determine if Costa’s Hummingbirds will come to urban areas to use native vegetation.
2. Determine what the limiting factors are for Costa’s in urban areas.
3. Study where Costa’s Hummingbirds winter.
4. Determine if there are any factors outside of AZ that could affect species on wintering grounds and on migration routes.
Gilded Flicker (Colaptes chrysoides)
Associated Species: Other species that may use similar habitat components or respond positively to management for the Gilded Flicker are: Purple Martin, Brown-crested Flycatcher, American Kestrel, Ash-throated Flycatcher, Verdin, Western Screech-Owl, Elf Owl, White-winged Dove, Gila Woodpecker, and Scott’s Oriole.
Distribution: The Gilded Flicker is resident from extreme southeastern and Baja California, southeastern Nevada, through central Arizona to northwest Mexico (Sonora and Sinaloa) from sea level to about 900 m (2955 ft). Throughout most of their range, Gilded Flickers are confined to desert scrub with large cacti (saguaro, organ pipe, cardon and hecho). In the northeastern portion of their range (southeastern and central Arizona) Gilded Flickers use riparian woodlands (cottonwood/willow) where large cacti are absent.
Ecology: The nesting period spans from February to June with nests frequently found in the upper 3 m (10 ft) of a giant cactus (Winkler and others 1995). Nest heights range from 2.5-12 m (8-40 ft), generally around 4.5 m (15 ft) (Bent, 1939). Cottonwoods, willows and snags are used where giant cacti are absent. From 3 to 5 eggs are laid indicating a lower reproductive rate than Northern Flicker (Colaptes auratus). Old nests are used by other species such as flycatchers and owls. Food includes ants and their larvae, other insects and fruit (e.g. cactus fruits). Flickers may cause some damage to pecan and walnut plantations (Winkler and others 1995). Gilded Flickers "suffer greatly from nest competition from" European Starlings (Sturnus vulgaris) (Winkler and others 1995).
Habitat Requirements: In Arizona the Gilded Flicker is primarily associated with saguaro and to a lesser extent with cottonwood at the edges of its range. Saguaros provide nesting substrate and food. Populations are densest where saguaros are abundant.
IMPLEMENTATION RECOMMENDATIONS AND OPPORTUNITIES
Management Issues with Conservation Recommendations
The spread of European Starlings into the desert Southwest has apparently caused declines in Gilded Flicker populations due to their intense competition for nest cavities. Large scale removal of desert scrub vegetation for subdivisions and agriculture, and the lack of recruitment of saguaros, has eliminated habitat for this species. Increased urbanization has, in some instances, increased the negative publicity towards woodpeckers in general due to their noisy vocalizations and destruction of expensive, planted saguaros. Conversion of cottonwood/willow riparian habitat to agriculture and invasion of the exotic salt cedar has likewise reduced the amount of habitat available, especially along the Colorado River. The spread of non-native grasses into desert scrub habitats has introduced fire where plants are not fire-adapted causing conversion from shrublands to grasslands. This is particularly true in Sonora where over 10% of the total land surface has been converted to non-native buffel grass spp. The rapid spread of red brome into Arizona desertscrub presents a similar threat.
Gilded Flicker management issues (potential) are listed in italics. Below each issue are the Arizona Partners in Flight Conservation Recommendations.
Habitat Loss
1. Encourage landowner/manager to maintain large saguaros and to protect all age classes for mature stands in the future.
2. Developers should be encouraged to leave larger tracts of saguaros (green-belts and open space).
3. Increase recruitment of saguaros.
Fire
1. Implement full suppression to maintain older saguaros.
2. Reduce fuel loads along roadways to reduce fire risk.
Implementation Opportunities
1. Educate general public about beneficial aspects of woodpeckers and how they can humanely discourage them from damaging property.
2. Control the number of starlings (gilded flicker competitors).
3. Educate stables and feedlots to control amount of available grain (encouraging starlings).
EVALUATION OF ASSUMPTIONS: RESEARCH AND MONITORING
Recommended Research
1. Determine the age/size-class needs of saguaros that are used for nesting.
2. Determine the minimum habitat requirement for species.
3. Determine if Gilded Flickers are adaptable to artificial nest sites.
4. Determine if competition for nest cavities is a limiting factor for Gilded Flickers.
5. Study the extent Gilded Flickers kill saguaros, and other impacts to saguaros.
Rufous-winged Sparrow (Aimophila carpalis)
Associated Species: Other species that may use similar habitat components or respond positively to management for the Rufous-winged Sparrow are: Cactus Wren, Curve-billed Thrasher, Black-throated Sparrow, Verdin, Black-tailed Gnatcatcher, Phainopepla, Pyrrhuloxia, and Northern Cardinal.
Distribution: In the United States, the Rufous-winged Sparrow is resident only in southcentral Arizona. It then occurs south through Sonora to central Sinaloa in Mexico. In Arizona it ranges from near Winkelman and southwest of Florence, southeast to Mammoth, and south to Nogales and west through the Tohono O’odham Nation and the Sauceda Mountains in Maricopa County (Monson and Phillips 1981; Arizona Breeding Bird Atlas, unpublished data). During eruptions, the Rufous-winged Sparrow has been found east to Sierra Vista, Tombstone and Saint David, Elgin and Gardner Canyon wash east of the Santa Rita Mountains, and west to Quitobaquito (Monson and Phillips 1981).
Ecology: The Rufous-winged Sparrows is non-migratory. It may be heard singing any time of the year, but in normal (dry) years, singing occurs from June or July to mid-September (Bent 1968). Territory size varies depending on resource availability and range from less than 0.5 ha (1 ac) to more than 1 ha (2 ac) per pair (Phillips in Bent 1968). Rufous-winged Sparrows have been found nesting from mid-April to mid-September with the bulk of nesting after initiation of summer rains in July. April and May nesting likely occurs only during those years with higher precipitation during the winter and early spring (ABBA unpubl. data, Bent 1968). Nests are often placed in desert hackberry, graythorn, cholla, mesquite, and clumps of mistletoe in paloverde between 0.15-2.5 m (0.5-8.2 ft) (Phillips in Bent 1968). In riparian and mesquite dominated habitats, cowbird brood parasitism has been as high as 50 percent (Bent 1968). During the nesting season a large proportion of the food includes small caterpillars and grasshoppers. They also catch low-flying insects in short sallies and glean others from the stems of small plants such as burroweed (Bent 1968). Food at other seasons presumably consists largely of grass and weed seeds (Bent 1968).
Habitat Requirements: Phillips (in Bent 1968), characterizes the habitat of Rufous-winged Sparrow as grass and thorny brush. This includes lush Sonoran Desert and washes with palo verde, ironwood, mesquite, desert hackberry, cholla, saguaro, burroweed and scattered grasses, as well as, semidesert grassland mixed with shrubby mesquite and acacia (Bent 1968). Rufous-winged Sparrows formerly preferred the Sonoran Savanna Grassland (Brown 1982), a habitat that has undergone a drastic reduction in Arizona and Sonora. It will also use shrub-dominated, former cropland and riparian bottomland, as long as grass is a major component (Phillips in Bent 1968). This species seems to prefer the flatter portions of the habitat and apparently does not use the steeper hillsides. Formerly more common in the Tucson Basin, Rufous-winged Sparrows disappeared for nearly 50 years from that area as a result of overgrazing (Phillips and others 1964). They were rediscovered in the Tucson Basin in 1936.
IMPLEMENTATION RECOMMENDATIONS AND OPPORTUNITIES
Management Issues with Conservation Recommendations
Conservation of the Rufous-winged Sparrow requires protection of grassland habitats particularly in core areas. While formerly common throughout the Tucson Valley, much of the core area for Rufous-winged Sparrow has been converted into urbanized habitats. Substantial portions of Rufous-winged habitat are subject to future development. Tubac Rita Ranch and other developments north of Nogales will also displace birds, therefore core areas will become of increasing importance in the future. Improper grazing that reduces or eliminates prime grass habitat will negatively effect Rufous-winged Sparrow population numbers and is strongly discouraged. Restrictions on floodplain development and retention of natural plant communities in floodplains will contribute positively to the conservation of this species.
Rufous-winged Sparrow management issues are listed in italics. Below each issue are the Arizona Partners in Flight Conservation Recommendations.
Habitat Loss/Alteration
1. Grazing management on state and federal administered lands that use alternate grazing regimes or light to moderate utilization in prime habitat.
Implementation Opportunities:
1. Coordinate with land managers to maintain appropriate levels of grazing.
EVALUATION OF ASSUMPTIONS: RESEARCH AND MONITORING
Recommended Research
1. Determine how urbanization affects this sparrow.
2. Study what causes sparrow irruptions.
3. Determine if predation is a problem.
4. Study to what extent Brown-headed Cowbird parasitism affects this species.
5. Determine if Rufous-winged Sparrows breed twice in different habitats (do populations in Sonoran Desert breed later in desert grassland?).
6. Determine if fragmentation affects this species.
Le Conte’s Thrasher (Toxostoma lecontei)
Associated Species: Other species that may use similar habitat components or respond positively to management for the Le Conte’s Thrasher are: Lesser Nighthawk, Black-throated Sparrow, Black-tailed Gnatcatcher, Verdin, Loggerhead Shrike, and Greater Roadrunner.
Distribution: The Le Conte’s Thrasher’s breeding range currently extends from Southern Nevada and Southwestern Utah to Southeastern California and Western/Southwestern Arizona, northeastern Baja and northwestern Sonora (AOU 1983, Sheppard 1996). This thrasher in uncommon and local throughout its range and is not known to be migratory (Phillips and others 1964, Rosenberg and others 1991, Sheppard 1996). Earlier accounts have documented the Le Conte’s Thrasher in Central and parts of Southeastern Arizona as well (Mearns 1886, Merriam 1895).
Ecology: Nesting generally occurs from February to June (Gilman 1904, Sheppard 1996) and several clutches are raised (Ehrlich and others 1988). Nests built of twigs and lined with two layers of flowers and fibers are commonly found in dense cholla cactus, creosote and palo verde (Ehrlich and others 1988, Gilman 1909, Merriam 1895).
Habitat Requirements: Nearly all Toxostoma species occur within the Colorado River basin (Mearns 1886). Le Conte’s Thrasher inhabits sandy desert washes, flats and dunes (Phillips and others 1964, Rea 1983). Surrounding vegetation is typically Ambrosia/Atriplex with some Prosopis and Cholla species (Rea 1983). Along the Gila River, areas inhabited by Le Conte’s are mostly dominated by creosotebush (Monson and Phillips 1964). The Le Conte’s Thrasher is the only avian species diagnostic of this sparsely vegetated Lower Colorado River Valley Subdivision of Sonoran Desertscrub (Brown 1994). This species forages entirely under desert shrubs (Sheppard 1996). Comparatively, the Crissal Thrasher (T. crissale) is common to dense Prosopis stands and forages within the branches of these bushes as well (Gilman 1909, Rea 1983).
IMPLEMENTATION RECOMMENDATIONS AND OPPORTUNITIES
Management Issues with Conservation Recommendations
Very little is known about the biology/ecology of the Le Conte’s Thrasher. The decline of this thrasher’s breeding range is largely attributed to habitat degradation involving the destruction of substrate, litter and shrubs. Shooting (near urban areas), DDT spraying (primarily in Mexico) and the improper use of some types of mist nets by ornithologists (60 mm mesh) may also be important factors in the decline of this species (Sheppard 1996). The Le Conte’s Thrasher has been designated as a Species of Special Concern by the California Department of Fish and Game and as a Category 2 candidate for possible listing by the USFWS (Sheppard 1996). Management recommendations would involve setting aside large areas of appropriate desert habitat. Although no steps have been taken to set aside habitat for this species, many conservation areas currently in existence and in planning may also meet the needs of Le Conte’s Thrasher (Sheppard 1996).
Le Conte’s Thrasher management issues are listed in italics. Below each issue are the Arizona Partners in Flight Conservation Recommendations.
Human Disturbance
1. Protect known at-risk breeding territories.
2. Avoid RV use on BLM land during Le Conte’s Thrasher breeding season.
Loss of Habitat
1. Protect large tracts of optimal Le Conte’s Thrasher desert habitat.
Implementation Opportunities
1. Restore abandoned agricultural fields.
EVALUATION OF ASSUMPTIONS: RESEARCH AND MONITORING
Recommended Research
1. Determine if Le Conte’s Thrasher’s will respond positively to rehabilitated farmland.
2. Conduct surveys in high-use areas with good thrasher habitat.
3. Evaluate use of artificial nest trees in areas where suitable sites may be limiting.
4. Determine the limiting factors for species, and why they are so locally distributed.
5. Study population and range trends.
Purple Martin (Progne subis)
Associated Species: Other species that may use similar habitat components or respond positively to management for the Purple Martin are: Brown Crested Flycatcher, Gila Woodpecker, Gilded Flicker, American Kestrel, Northern Cardinal, House Finch, Elf Owl.
Distribution: The Purple Martin breeds from southwestern British Columbia south to Baja California; and from northeastern British Columbia to New Brunswick south to Mexico, the Gulf Coast, and southern Florida. Local in the Rocky Mountains but avoids most other mountainous areas (DeGraff and others 1991). Winters in South America east of the Andes from Venezuela south to northern Bolivia and southeastern Brazil (Ehrlich and others 1988). In Arizona, breeds in the Transition Zone of open habitats of the entire Mogollon Plateau region, extending to Williams, Mount Trumbull, the Natanes Plateau, the Sierra Ancha, and the Prescott region. Also found in the Chiricahua Mountains but absent from other mountains of southern Arizona, the Grand Canyon, and the northeast. Also in saguaro associations of south-central Arizona west to the Ajo Mountains and north to near Picacho, Florence, Roosevelt Lake, and the lower San Pedro Valley. Rare outside the breeding ranges (Phillips and others 1964).
Ecology: Purple Martins arrive in Arizona in early April and remain until early October (Phillips and others 1964). In the Arizona Upland subdivision of the Sonoran Desert, Purple Martin’s nest primarily in old woodpecker holes in larger and older saguaros (Phillips and others 1964). Most nests are placed in the main stem of the saguaro within 3 m of the top (Brown 1997) and no more than one pair per saguaro has been found in Arizona (Brown 1997). Purple Martins also nest in tree cavities excavated by woodpeckers, and occasionally in cliff niches. They use colonial birdhouses in the eastern United States but have not adapted to these in the west, where they tend to nest singly (Brown 1997, Phillips and others 1964). The nest is made up of grass, leaves, mud, feathers, and occasionally has a dirt rim to keep eggs from rolling out. Fresh green leaves added during incubation are thought to be used for their pesticidal properties. Cowbird parasitism is very rare.
Purple Martins feed on flying insects taken on the wing often at altitudes over 50 m (164 ft), and may occasionally feed on the ground. Food items include ants, wasps, beetles, grasshoppers, stink bugs, treehoppers, dragonflies, moths, butterflies, mosquitoes, horseflies, robber flies, etc. Typically, they don’t forage when temperatures are less than 9° C (48° F) or in the rain. If cold or adverse weather lasts more than 3-4 days, mortality can be substantial (Brown 1997). They drink and bathe on the wing (Ehrlich and others 1988). They gather in enormous premigratory communal roosts at the end of summer, which may include up to 100,000 birds (Ehrlich and others 1988).
Considered as two subspecies in Arizona, exhibiting ecological races. Martins inhabiting the saguaro deserts (P.s. hesperia, used tentatively by Phillips, 1964) are of decidedly smaller size than those found in north and central Arizona (P.s. arboricola). The two habitats (and distributions) are in close proximity in the Roosevelt and Coolidge Lake areas.
Habitat Requirements: Purple Martins in the Upper Sonoran Desert are closely associated with saguaro forests. They will forage and roost in areas adjacent to cactus forests, including towns, parks, lakes and ponds. In central and southeastern Arizona, Martins inhabit open and cut over woodlands, open grassy river valleys, meadows around pools, shores of lakes, marsh edges, agricultural lands, parks and towns. Where trees are the nesting substrate, they prefer stands with both living and dead trees (Brown 1997). Purple Martins need a high old-growth snag density adjacent to or in open areas preferably near open water.
IMPLEMENTATION RECOMMENDATIONS AND OPPORTUNITIES
Management Issues with Conservation Recommendations
Audubon Society Blue List 1975-1981, Special Concern 1982-1986. Increased development and fire in Upland Sonoran Desert habitat could pose threats to P.s. hesperia, by reducing nest site availability in large saguaro forests. Forestry practices that removed standing dead trees greatly reduced the availability of natural nest sites for P.s. arboricola. Since they do not use colonial nest boxes in western states, they suffer from a lack of nest sites in many areas. House sparrows and starlings compete for nest cavities and can cause local extirpation. Brawn and Balda (1988) state that the Purple Martin has nearly been extirpated from the ponderosa pine forest since fire suppression has resulted in much denser conditions and logging has reduced the number of snags and large old trees. Currently nests only in clusters of old, dead pines containing numerous woodpecker holes. Pesticide use in South America is a potential threat to wintering birds.
Purple Martin management issues, in Upland Sonoran Desert habitat, are listed in italics. Below each issue are the Arizona Partners in Flight Conservation Recommendations.
Habitat Loss
1. Encourage landowner/manager to maintain large saguaros and to protect all age classes for mature stands in the future.
2. Urge developers to leave larger tracts of saguaros (green-belts and natural open space).
3. Increase recruitment of saguaros.
4. Promote county land planning to minimize impacts on adjacent natural habitats and encourage natural components.
Fire
1. Reduce fuel build-up in Upland Sonoran Desert habitats to protect against catastrophic fire.
EVALUATION OF ASSUMPTIONS: RESEARCH AND MONITORING
Recommended Research
1. Research the population distribution of Purple Martins to learn more about habitat range.
2. Determine if pesticides are a threat in Upland Sonoran Desert habitat.
3. Study what specific prey items are used.
4. Study colonial nesting and competitive interactions with other species.
5. Study premigratory communal roost habitat requirements and localities.
Outreach Needs:
1. Discourage starlings around possible or know martin nesting areas to reduce competition.
2. Educate stables and feedlots to control amount of available grain (encouraging starlings).
3. Request local birders to report breeding and roost locations.
4. Provide information to Land Managers about habitat needs.
4. Coordination of Recommendations and Opportunities in Sonoran Desertscrub
Unlike many of Arizona’s major habitats, we are in a rather unique situation with Sonoran Desertscrub habitat in that much of it is still in good condition and most of the birds using it are stable. We are in a position of being proactive and have the opportunity to prevent or slow down impending habitat loss by recognizing the threats now before it is too late. It is also our responsibility to protect Sonoran Desert in Arizona, since we have more than one third of its entire range and by far, the most Sonoran Desert in all of the continental United States.
The battle between urban growth and conservation of natural resources has escalated nationwide and Arizona is no exception. Urban growth combined with nonnative grasses that provide fuel to this non-fire-adapted habitat, could destroy this unique ecosystem over time if we don’t have some measures in place to prevent this from happening. The clues are already reaching us as we learn more about Sonoran Desertscrub birds that disappear from habitat that appears adequate but lies on the edge of urban areas (Emlen 1974, Tweit and Tweit 1986, Mills and others 1989, Stenberg 1988, Germaine 1995, Frederick 1996). The conflict is only too real for the residents of Tucson as many fight for the right to develop in what has been identified as key habitat for the endangered Cactus Ferruginous Pygmy-Owl. The pygmy-owl was the only bird recognized as a real "priority" in Sonoran Desertscrub habitat at this time. Recommendations were also made for the five other species that are currently stable but highly dependent on this habitat for their survival.
For the Cactus Ferruginous Pygmy-Owl, habitat loss is the primary threat. Restoring and maintaining existing habitat is recommended for not only the Pygmy-Owl, but for all Sonoran Desertscrub dependent species. Maintaining existing habitat includes reducing the risk of wildfire. Roadsides are perhaps the most common place for desert wildfires to start due to increased amounts of brush that accumulate in these disturbed areas, and from burning cigarettes thrown out of car windows. Recommendations for full fire suppression where possible, and reduction of fuel loads along roadways, are made for all species.
The issue of urbanization will likely increase for more and more species as we continue to develop into natural areas. To maintain a healthy diversity of birds, as well as other wildlife, regional planning should incorporate the habitat needs of key species. Where development is inevitable, maintaining large tracts of natural, native open space adjacent to urban areas and using native vegetation when replanting is recommended. Education of bird enthusiasts and other recreationists about the possible sensitivity of human disturbance to the Cactus Ferruginous Pygmy-Owl, is also recommended.
Table 14. Sonoran Desertscrub Priority Species and Habitat Needs
Bird Species |
Vegetation Composition |
Vegetation Structure |
Abiotic Factors |
Landscape Factors |
Cactus Ferruginous Pygmy-Owl (priority) |
-(in Arizona Upland) Saguaro, ironwood, paloverde, mesquite, cholla, creosote, bursage |
(in Arizona Upland) -prefer dense foliage from ground to canopy -moderate to high ground cover appears to be needed for prey base -high plant species diversity -diverse structure including a large shrub or tree component. (See AGFD Cactus Ferruginous Pygmy-Owl Tucson habitat study.) |
-below 1220 m (4000 ft) -may be associated with water due to increase prey base (increase water sources near residential areas. -flats to upper alluvial fans (bajadas) |
-fragmentation effects unknown -patch size - rough estimates : 4-8 ha (10-20 ac) territory in breeding season up to 80+ ha (200+ac) in non-breeding season (Tucson, Organ Pipe) -late successional stage |
Costa’s Hummingbird (not priority) |
paloverde, saguaro, mesquite, ocotillo, wolfberry, catclaw acacia, chuparosa, ironwood, creosote, desert-willow, jojoba |
-prefer small, dense trees or shrubs, (ave. 4.3 m (14 ft)) tall, ABBA unpubl. data) -nest on lower half of trees (especially paloverde) ave. 2.2 m (7.2 ft) (ABBA unpubl. data) |
-population more productive in wet winters from availability of more flowering vegetation and subsequent higher availability of insects. -may construct nests later in season away from sun exposure. |
-fragmentation. - not necessarily a factor -found most commonly in ecotone between riparian and desert flats (in LCRV) -mid- to late successional stages -appears to forage and nest in (close) proximity to tubular flowers |
Gilded Flicker (not priority) |
saguaro, paloverde, mesquite, ironwood |
-use saguaro (roughly) over 80 years old |
-larger saguaros mainly occurring on southerly and westerly facing slopes |
-drop out in urban areas, unlike Gila Woodpecker -fire eliminating older, and larger saguaros could become a threat |
Purple Martin (not priority) |
saguaro, ironwood, mesquite, paloverde, graythorn, desert hackberry, triangle-leaf bursage, cholla |
-use saguaro (roughly) over 80 years old, with many cavities |
-larger saguaros mainly occurring on southerly and westerly facing slopes |
-prefer areas with denser and older stands of saguaros -can use urban/rural edge if stands of saguaros are present -historically roosted in large cottonwoods, now commonly found (post breeding) on electrical wire |
Le Conte’s Thrasher (not priority) |
creosotebush, white bursage, paloverde, mesquite (velvet and honey), smoketree, ironwood, saltbush |
-dense low to mid-story shrubby trees that are isolated in open areas |
-slope- flat or little topography -in AZ, the majority of them occur below 305 m (1000 ft) |
-fairly local in occurrence -need isolated, scattered trees for nesting and perches -need open ground for running |
Rufous-winged Sparrow (not priority) |
paloverde, mesquite, bursage, graythorn, prickly pear, desert hackberry, cholla, barrel cactus |
-nest in lower third of trees -usually occur where ground cover and understory are present in above average percentages |
-annual precipitation may influence range (affecting grass and understory component) -Sonoran Desert habitat may be a secondary habitat (primary habitat being in area with more consistent grasses) -gentle to flat slopes |
-populations are not continuous, local depending on grass and understory component -successional stages: mid would be primary, early would be secondary |
Table 15. Special Factors for Sonoran Desertscrub Priority Species
Bird Species |
Special Factors |
Cactus Ferruginous Pygmy-Owl (priority) |
-needs cavities (secondary cavity nester); may need higher density of cavities. -competition with other secondary cavity nesters |
Costa’s Hummingbird (not priority) |
-this species does not benefit as much from urban feeders as other hummingbird species (i.e. Anna’s, Black-chinned) -closely tied to native vegetation -majority of males leave the nesting areas by late spring |
Gilded Flicker (not priority) |
-nest cavity competition with starlings and screech owls may be a factor -since Gilded Flicker construct larger cavities, they sometimes cause saguaro to die -tend not to excavate cavities in the same saguaros as Gila Woodpeckers, which may represent competition for nesting saguaros |
Purple Martin (not priority) |
-colonial nesters -secondary cavity nesters -long distance migrants -need old, large saguaros with many cavities -may be associated with Gila Woodpeckers -nest later than all other saguaro cavity breeders which may aid in avoiding competition |
Le Conte’s Thrasher (not priority) |
-very sensitive to human disturbance -primarily ground-feeding (cursorial) predator -can use more open and dryer habitat more effectively than similar species -will commonly use same nest tree but build new nest each year |
Rufous-winged Sparrow (not priority) |
-associated with grass, forbes, and denser understory (in good years of winter rains) -feeds on insects, seeds -is eruptive in some years |