Habitat
Breeding habitats include warm/hot, semi-arid, shrubby habitats, especially mesquite and brushy pinyon-juniper woodlands; also chaparral and desert scrub. Thorn scrub, oak-juniper woodland, pinyon-juniper, juniper-cholla, mesquite, dry chaparral (Bent 1950, AOU 1983). Builds cup nest suspended from forked twig in a shrub or tree 0.5 to 2 meters tall (Ehrlich et al. 1988); nest usually 0.5-3.5 meters above ground.
In New Mexico, breeding occurs in rocky hills covered with sparse bushes and scrub, in juniper, hackberry (Celtis spp.) and Grave's oak (Q. gravesi; Bailey 1935, Barlow 1977). In northwestern New Mexico, found at elevations from 5800 - 7200 feet in broad-bottomed canyons (flat or gently sloped valleys) below or near ridge-top/rock outcrop/cliff head walls of canyons or gently sloped bowls in pinyon-juniper woodland (Reeves 1998). The pinyon-juniper is sometimes dense canopied woods and at other times widely-spaced trees creating parkland. Trees are generally mature ranging from 12 to 25 feett in height. Other shrubs species include Utah Serviceberry (Amelanchier utahensis) and Antelope brittlebrush (Purshia tridentata). There is often considerable bare soil between herbaceous plants forming ground cover. At the upper elevation, ponderosa pine (Pinus ponderosa) is sparsely situated among pinyons and junipers (Reeves 1998).
In Arizona, gray vireos frequent juniper (Juniperus spp.) habitats of Upper Sonoran Zone, also mesquite (Prosopis spp.); usually they prefer large juniper or chaparral with scattered trees (Phillips 1964). In southern Nevada, these birds occur in pinyon, juniper and sagebrush (Artemisia spp.) with additions of mountain mahogany (Cercocarpus ledifolius), Gambel oak (Quercus gambelii), Mexican manzanita (Arctostaphylos pungens), squaw apple (PERAPHYLLUM RAMOSISSIMUM), and cliffrose (COWANIA STANSBURYANA; Johnson 1972, cited in USDA Forest Service 1994). In Big Bend National Park, Texas, gray vireos occur in lower chaparral between 1219 and 1676 meters (4000 to 5500 feet elevation); they nest in Gregg's ash (FRAXINUS GREGGII) and evergreen sumac (RHUS VIRENS; Barlow 1977, Wauer 1977). In Joshua Tree National Monument and eastern Mojave Desert, California, they occurred in pinyon-juniper or pinyon-juniper mixed with sagebrush. In southern California (San Jacinto area), habitat includes chaparral dominated by chamise (ADENOSTOMA FASCICULATUM) or redshanks (A. SPARSIFOLIUM); also scrub oak, manzanita (ARCTOSTAPHYLOS spp.), CEONOTHUS, pinyon, and sagebrush. In Laguna Mountains, California, gray viroes were recorded in chamise and CEONOTHUS GREGGII (USDA Forest Service 1994).
In migration and winter, gray vireos occur in habitats to those used during the breeding season; also desert and arid scrub, chaparral, brushy scrub in pinyon-juniper woodland, semi-open areas with scattered scrub and semi-open arid brushland (AOU 1983, Terborgh 1989, Howell and Webb 1995). Winter range closely overlaps the range of one species of elephant tree, BURSERA MICROPHYLLA, throughout the coastal deserts surrounding the Gulf of California. A study in Sonora, Mexico, found heavy dependence on B. MICROPHYLLA fruits, which are available in quantity from September through April. Only one disjunct wintering population occurs outside the range of B. MICROPHYLLA (Bates 1992a), in the Chisos Mountains, Big Bend National Park, Texas, in habitat dominated by Texas persimmon (DIOSPYROS TEXANA) mixed with honey mesquite (PROSOPIS JULIFLORA), whitethorn acacia (ACACIA CONSTRICTA) and other shrubs (Barlow and Wauer 1971).
Ecology
Territories observed by Barlow (1977) ranged from 2.4 to 8 hectares in the northern Chihuahuan Desert and in Yavapai County, central Arizona. Barlow (1997) noted a singing male every 300 meters over a distance of 15 kilometers.
May be a principle seed disperser for B. MICROPHYLLA, and the close overlap between their ranges suggests a possible mutualism (Bates 1992a). Feeds on its fruit which are available in quantity from September through April. Both males and females defend territories in winter, and individuals will return to the same winter territory in successive years; nine territories were 0.3-1.4 hectares (mean 0.9 hectares; Bates 1992b).