Western tanager

Last updated

Western tanager
Western Tanager (male).jpg
Adult male in breeding plumage
Piranga ludoviciana female.jpg
Adult female
Song
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Aves
Order: Passeriformes
Family: Cardinalidae
Genus: Piranga
Species:
P. ludoviciana
Binomial name
Piranga ludoviciana
(Wilson, 1811)
Piranga ludoviciana map.svg
Range
  Summer breeding range
  Migration
  Winter non-breeding range

The western tanager (Piranga ludoviciana), is a medium-sized American songbird. Formerly placed in the tanager family (Thraupidae), other members of its genus and it are classified in the cardinal family (Cardinalidae). The species's plumage and vocalizations are similar to other members of the cardinal family.

Contents

Taxonomy

The western tanager was illustrated and formally described by American ornithologist Alexander Wilson in 1811 under the binomial name Tanagra ludoviciana from a specimen collected on the Lewis and Clark Expedition (1803-1806). [2] The type locality is Kamiah, Idaho. [3] [4] The specific epithet is from the Late Latin ludovicianus for "Louis". The name is from Louisiana, the 18th-century French administrative district of New France, rather than the modern state. [5] The western tanager is now placed in the genus Piranga that was introduced by French ornithologist Louis Pierre Vieillot in 1808. [6] [7] The species is monotypic; no subspecies are recognized. [7]

Description

Measurements:

Adults have pale, stout pointed bills, yellow underparts, and light wing bars. Adult males have a bright red face and a yellow nape, shoulder, and rump, with black upper back, wings, and tail; in non-breeding plumage, the head has no more than a reddish cast and the body has an olive tinge. Females have a yellow head and are olive on the back, with dark wings and tail.

The song of disconnected short phrases suggests an American robin's, but is hoarser and rather monotonous. The call is described as pit-er-ick.

Their breeding habitat is coniferous or mixed woods across western North America from the Mexico-U.S. border as far north as southern Alaska; thus, they are the northernmost-breeding tanager. They build a flimsy cup nest on a horizontal tree branch, usually in a conifer. They lay four bluish-green eggs with brown spots.

These birds migrate, wintering from central Mexico to Costa Rica. Some also winter in Southern California.

Distribution and habitat

The breeding range of the western tanager includes forests along the western coast of North America from southeastern Alaska south to northern Baja California, Mexico. Western tanagers extend east to western Texas and north through central New Mexico, central Colorado, extreme northwest Nebraska, and areas of western South Dakota to southern Northwest Territories, Canada. [10] [11] [12] The western tanager's wintering range stretches from central Costa Rica north through Nicaragua, Honduras, El Salvador, and Guatemala to southern Baja California Sur and extreme southeastern Sonora in western Mexico and to southern Tamaulipas in northeastern Mexico. Western tanagers do not typically occur in the Caribbean lowlands. They have been reported wintering further north and have been observed as far south as Panama. [10] [11] [12] Vagrants are rare to casual in the eastern United States. [13]

In addition to the plant communities listed above, western tanagers are reported from disturbed habitats. For instance, western tanagers were seen in an area of northwestern California that had been logged less than five years previously. Cutleaf burnweed (Erechtites glomerata) was characteristic of the youngest age class, while slightly older sites were composed predominantly of tanoak (Lithocarpus densiflorus) with smaller amounts of snowbrush ceanothus (Ceanothus velutinus), whitebark raspberry (Rubus leucodermis), and Sierra gooseberry (Ribes roezlii). [14] In addition, western tanagers were captured along the Rio Grande in New Mexico during spring and fall migration in an agricultural area composed primarily of alfalfa (Medicago sativa) and corn (Zea mays). [15]

Western tanagers have also been observed in saltcedar (Tamarix species) communities [15] and in Russian olive (Elaeagnus angustifolia) vegetation. [15] In New Mexico, western tanagers were observed in nearly pure stands of saltcedar 10 to 23 ft (3–7 m) tall. Western tanagers were also observed in saltcedar communities during fall migration in along the Rio Grande. [15] Ten western tanagers were observed among three sites composed of Russian olive in Colorado, Utah, and Idaho. All sites were dominated by Russian olive with cheatgrass (Bromus tectorum) comprising a substantial portion of the understory. Along the Rio Grande, western tanagers were most often captured during fall migration in vegetation with a Rio Grande cottonwood ( Populus deltoides species wislizenii) overstory and a moderate to dense Russian olive understory. [15]

Behavior and ecology

Western tanagers migrate alone or in groups of up to 30 birds. [11] [12] On average, hatching-year western tanagers were captured later (early September) at Rio Grande Nature Center than adult western tanagers (mid-August) during fall migration. Migration timing, condition of birds, and site differences in spring and fall migration were also addressed in this investigation. [15]

Breeding

Western tanagers arrive on their breeding grounds in spring. Breeding usually occurs among birds two years or older, beginning in May and continuing into July, although some first-year western tanagers also breed. [11] [12] In the Sandia Mountains of north-central New Mexico, western tanagers were heard singing beginning in late May, and the first nest was found in early June. [16] In public open-space areas in Boulder County, Colorado, the start of the western tanager breeding season was estimated as 28 May, and the peak of the breeding season, defined as at least 50% of western tanager nests active, was from 6 June to 1 July. [11] [17] In the Southwest, brooding generally begins in early May, while in the Northwest, brooding starts typically in mid-June. Brooding can begin earlier in British Columbia and Alberta than in the northwestern United States. An egg-laying date as early as 16 May in British Columbia was estimated by back calculation, and a complete egg set was observed as early as 26 May in Alberta. [11]

Cup nests are built by the female, take about four or more days to construct, and are made from twigs, rootlets, grasses, and pine needles. [11] [12] No evidence has been found for second broods in western tanagers, but a review notes a nesting attempt after a failed nest in west-central Idaho, and suggests that renesting is a substantial source of late nesting attempts. In addition, renesting was suggested as the explanation for a few late nests observed in Boulder County, Colorado. [11] [17]

Clutch size is typically three to five eggs. [11] [12] [17] Average clutch size in 10 nonparasitized nests in Boulder County was 3.8 eggs. [17] Average clutch in the Southwest may be smaller than that of western tanagers nesting in the north. [11] Egglaying generally takes about one day per egg. [11] The female incubates the eggs for about 13 days, although shorter incubation periods have been reported. The young are fed by both parents, and typically fledge 11 to 15 days after hatching. [11] [12] [17] Immature western tanagers have been observed with the parents at least two weeks after fledging. [11]

Immature western tanagers initiate migration later than adult birds. Generally, western tanagers leave more northerly locations in late summer or early fall, while those in more southerly areas may stay as late as early November. [11]

Reproductive success of western tanagers varies widely between studies and across years. An average annual nest success probability estimate is 0.186 over 3 years, with a low of 0.035 and a high of 0.349. [11] In a northern Arizona study area, an average of 43% (n=7) of nests succeeded to the nestling stage. In Boulder County, nesting success varied from 11.3% to 75.3%, with an average of 51.8% over a 3-year period. [17] Daily nest survival rate on ungrazed sites in northeastern New Mexico was 0.955, which was not significantly (p<0.05) different from the 0.973 daily nest survival rate found on grazed sites. Nest predation is the leading cause of nest failure. Predation rates ranged from 30% (n=48) in a study in New Mexico pinyon-juniper woodland to 86% (n=14) in a mixed-conifer forest in Idaho. [11]

Western tanagers can live several years. The annual average survival rate is 0.753 and a return rate is 30.1% for western tanagers in west-central Idaho. [11] A wild western tanager 7 years and 11 months old has been documented from banding data. [18]

A male enjoying the fruits of a cherry tree. Western Tanager-male-Oregon-cherry.jpg
A male enjoying the fruits of a cherry tree.

Habitat

During the breeding season, western tanagers are found primarily in relatively open coniferous forests and mixed woodlands. [10] [11] During migration, western tanagers occur in more areas, including lowland woodlands of Southern California, desert oases, riparian areas, parks, and orchards. [11] In the western tanager's wintering range, it occupies pine (Pinus spp.) and pine-oak (Quercus spp.) woodlands, as well as low-canopied scrub forests, forest edges, and coffee plantations. [12]

Western tanagers breed at a wide range of elevations from about 183 ft (56 m) in the Northwest up to 10,000 ft (3,050 m). [10] [11] In the northern portion of their breeding range, western tanagers have been observed on sites over 8,300 ft (2,530 m) in Oregon down to sites as low as 183 ft (56 m) in Oregon's Central Willamette Valley. [19] In the southern portion of their breeding range, western tanagers are more typical on high-elevation sites. [12] They were observed on an Arizona site 8,270 ft (2,520 m) in elevation and on a site at 9,500 ft (2,900 m) in Nevada. [20]

Nesting

Western tanagers nest in second-growth and mature conifer and mixed forests. They only breed in stands of pole- to large-sized trees and stands of pole- to medium-sized trees with >70% canopy cover. [21] Nesting was confined to older second-growth (>40 years) and mature (120+ years) Douglas fir (Pseudotsuga menziesii) communities in the western Cascade Range in Oregon. [22]

Western tanager nests are typically found in coniferous trees toward the end of horizontal branches and at heights greater than 10 ft (3 m); 79% of 43 western tanager nests in British Columbia were found in conifers, primarily Douglas fir. [11] The deciduous trees most often used were quaking aspen (Populus tremuloides) and willows (Salix spp.). The position of their nests along the branches of deciduous trees was more variable than in conifers. On this site, 56% of nests were at heights from 21 to 36 ft (6.4–11 m). Of 9 western tanager nests in an Alberta study site, eight occurred in white spruce (Picea glauca) and one was found in quaking aspen. Nest height ranged from 20 to 42 ft (6.3–12.8 m), with a mean of about 30 ft (9.3 m). On average, nests were located 80% of the distance from the trunk to the tip of the branch. Of 49 western tanager nests found in a pinyon-juniper (Pinus-Juniperus spp.) woodland in northeastern New Mexico, 98% were in Colorado pinyon (P. edulis) and the remainder occurred in Douglas fir. On this site, nest trees averaged 24 ft (7.4 m) in height and over 8 in (21.9 cm) in diameter at breast height (dbh). The average height of nests was 18 ft (5.4 m). In a nearby mixed-conifer forest, nests were found in Douglas fir and ponderosa pine (P. ponderosa). Nest trees on this site averaged nearly 50 ft (15.1 m) in height and 13 in (32.7 cm) in dbh. The average nest height was 16 ft (4.93 m) and on average nests were located about 5 ft (1.49 m) from the tree stem and 3 ft (0.97 m) from the edge of the tree's foliage. [11] Western tanager nests on a north-central New Mexico site occurred at heights from 8 to 15 ft (2–5 m), typically in white fir (Abies concolor) located in open areas. [16] In Idaho, nests were found in conifers at an average height of 40 ft (12.3 m) and ranged from 8 to 55 ft (2.4–16.8 m). Of 58 nests at a Colorado study site, 54 occurred in ponderosa pine and four were found in Douglas fir. [17] Nest height was significantly associated with tree height, with the mean nest height around 54% of tree height. On average, western tanager nests were located 63% of the distance between the trunk and the branch tip. This is closer to the bole than found in most studies, and the authors suggest that the conical shape of the ponderosa pine requires nests be placed closer in toward the trunk to provide cover. Canopy cover at nest sites averaged 71%, with a minimum of 31% cover. [17]

Foraging habitat

Female in a callery pear tree Western tanager in Chelsea (75305)2-2.jpg
Female in a callery pear tree

Western tanagers forage in many habitats, in all successional stages from grass-forb communities to stands of large trees with greater than 70% cover. [21] In western Oregon, they were not observed using the grass and forb successional stages, but were observed foraging in areas not used for nesting, such as shrub/sapling and young second-growth (16–40 years old) stands typically made up of Douglas fir. [22]

Although western tanagers forage in many habitats, they are typically observed foraging in forest canopies. For instance, in an area of California primarily dominated by giant sequoia ( Sequoiadendron giganteum ), western tanagers spent 60% to 75% of their foraging time above 35 ft (10 m) and less than 2% of foraging time below 12 ft (4 m). [23] In coniferous forests of western Montana, they were typically observed foraging in canopy foliage above 26 ft (8 m). In mixed conifer-oak forests in California, they foraged from 16 to 92 ft (5–28 m). [24]

In primarily Douglas fir-dominated vegetation in British Columbia, the occurrence of western tanager foraging in various portions of trees and the size of those trees were investigated. [25] This species perched on stems less than 1 in (<2.5 cm) in diameter in 96.9% of observations. Nearly 85% of observations were either near the branch tip or in the middle of the branch. Western tanagers foraged on larger trees, with nearly 80% of observations on trees with a trunk diameter of more than about 8 in (20.0 cm), and over 80% of observations occurring on trees 33 ft (10 m) or taller. They used taller trees and trees with larger diameters significantly more than their availability in all silvicultural treatments analyzed. [25]

Western tanagers may preferentially forage on certain species. In a California study of foraging and habitat relationships of insect-gleaning birds in mixed conifer-oak forest, they used white fir more and incense-cedar (Calocedrus decurrens) less than would be expected from their availability. Sugar pine (Pinus lambertiana), Douglas fir, and California black oak (Quercus kelloggii) were used slightly more than their availability, but this was not considered significant, since 95% confidence intervals overlapped with use in accordance with availability. Ponderosa pine was used in proportion to its availability. [24] In mostly Douglas fir-dominated communities in British Columbia, western tanagers were observed foraging in Douglas fir in 88.9% of observations, ponderosa pine in 7.4% of observations, and in living trees of other species in 3.7% of observations. Over all sites, the preference for Douglas-fir was significantly (p<0.001) greater than availability. When sites were separated by the various silvicultural treatments, only the 3-year-old light cut (Douglas fir and ponderosa pine larger than 14 in (35 cm) in dbh and other species larger than 6 in (15 cm) dbh were harvested) and the selectively logged (20% of 6- to 8-in dbh (15.2–20.3 cm) trees, 25% of 8- to 12-in dbh (20.3–30.5 cm) trees, 45% of 12- to 24-inch dbh (30.5–61.0 cm) trees, and 75% of >24-inch dbh (>61.0 cm) trees were removed) sites showed significantly greater use of Douglas fir by western tanagers than would be expected from availability. They were reported foraging on quaking aspen, as well as balsam poplar (P. balsamifera ssp. balsamifera), speckled alder (Alnus rugosa), and white spruce in central Alberta. [11]

Although western tanagers occur in stands of varying ages and have been observed in higher densities on young sites, [14] they are typically detected more often in relatively mature stands. For example, they appear to occur more often in mature (50–60 years old) and old-growth (100+ years) quaking aspen than young (<23 years old) trembling aspen stands in the Prince Rupert Forest Region of British Columbia. [26] In Alberta, western tanager was detected significantly (p<0.001) more often in old (120+ years old) quaking aspen mixed-wood stands than in mature (50–65 years old) or young (20–30 years old) mixed-wood stands. [27] The same trend has been found in other communities. In Washington, western tanager was observed on sites dominated by older (35-year- and 60-year-old) red alder (A. rubra), but not on sites containing young (4-year- and 10-year-old sites) red alder. [19] Although western tanagers were fairly common on recently harvested sites, they were detected at the most points in "mature" and "old-growth" ponderosa pine in northern Idaho and western Montana. Western tanagers had higher densities in mature (33 ft, >10 m tall) conifer plots and young conifer/mature conifer transition plots than in young (3–33 ft, 1–10 m tall) conifer plots in British Columbia. Western tanagers occurred at an average density of 53.2 birds/100 ha in sawtimber Douglas fir stands (>80–150 years old), 37.0/100 ha in mature Douglas fir stands (>100 years old), and 3.1/100 ha in sapling Douglas fir stands (<20 years old) in northern California. Although they occurred at higher densities in young Douglas fir forest in Oregon, the stands were 40 to 72 years old. Mature forest was from 80 to 120 years old, and old-growth forest was 200 to 525 years old.

Stand structure and composition

Western tanager in the Seedskadee National Wildlife Refuge Western tanager at Seedskadee National Wildlife Refuge.jpg
Western tanager in the Seedskadee National Wildlife Refuge

Western tanagers appear to prefer large trees, which are considered an important component of stands for them. [28] In addition, western tanagers were significantly positively associated with large saw timber (>20% cover, >21 in [>53.2 cm] mean dbh) and significantly negatively associated with pole timber (>20% cover; conifers >10 ft [>3 m] tall and 4–12 inh (10.2–30.4 cm) mean dbh; hardwoods 10–50 ft (3–15 m) tall and 4–12 in mean dbh) stands dominated by Douglas fir, western hemlock (Tsuga heterophylla), and red alder in the central Oregon Coast Ranges. In primarily Douglas fir-dominated communities in British Columbia, western tanagers foraged in trees >33 ft (>10 m) tall in more than 80% of observations, and nearly 80% of foraging observations were in trees with trunk diameters greater than 8 in (>20.0 cm). In addition, western tanagers foraged in trees smaller than 33 ft (10 m) tall less than their availability. [25]

Most evidence suggests that western tanagers prefer areas with moderate canopy cover. They avoid continuous canopy. [21] Stands with large trees and 40 to 69% canopy cover are an optimal western tanager habitat. Large trees and canopy cover ≥70% is considered suitable habitat, while areas with large trees and <40% cover are categorized as marginal habitat. In sapling/pole and mature ponderosa pine habitats of the Black Hills in South Dakota, western tanagers occurred at the highest densities in stands with intermediate (40%-70%) canopy cover. [29] In 35- to 45-year-old Douglas fir and red alder-dominated stands, an average of 322% more western tanagers were detected on sites logged to a density of 240 to 320 trees/ha, and an average of 363% more of them were detected on sites logged to a density of 180 to 220 trees/ha, compared to controls with 410 to 710 trees/ha. The difference in western tanager detections between the logging treatments and the control grew larger over time. In Arizona, western tanagers occurred at significantly higher densities (15.8/40 ha) in forest dominated by Douglas fir and ponderosa pine the year after logging to an average of 167.7 trees/ha compared to control stands (7.7/40 ha) with average tree density of 626.2 trees/ha. Western tanager densities on the treatment and control sites were more similar the following year. In British Columbia, western tanagers occurred at significantly higher densities after "light" logging on a site containing Douglas fir and ponderosa pine. The species apparently was positively influenced by thinning a ponderosa pine stand by 20% in Arizona. In the Sierra Nevada of California, western tanagers occurred at a higher density in an open-canopied (602 trees >10 cm dbh/ha) mixed-conifer stand consisting of Jeffrey pine (Pinus jeffreyi), lodgepole pine (P. contorta), white fir, and incense-cedar compared to a closed-canopied (994 trees >10 cm dbh/ha) mixed conifer stand of incense-cedar and white fir. This same pattern was found in open- (420 trees > 10 cm dbh/ha) and closed-canopied (658 trees > 10 cm dbh) California red fir (Abies magnifica var. magnifica) stands.

Western tanagers have been reported to prefer areas with a diverse forest structure, but importance of lower forest layers is unclear. In the Black Hills of South Dakota, they were significantly more abundant in multistoried habitats with bur oak (Q. macrocarpa) and quaking aspen/paper birch (Betula papyrifera) under a ponderosa pine canopy than in sapling/pole or mature ponderosa pine stands with varying canopy cover. [29] Reviews assert the importance of a diverse forest structure [28] and a dense deciduous understory [21] for western tanagers. In some areas, though, the influence of lower forest layers may be relatively insignificant. For example, removal of incense-cedar and white fir from 1 to 10 ft (0.3–3 m) tall in giant sequoia forests had little impact on western tanager density. [23]

Western tanagers may associate with or avoid some plant species. For example, in mixed-wood forests in Alberta, western they were significantly positively associated with conifer density. [27] The western tanager was also considered a conifer-associated species in quaking aspen-dominated and mixed quaking aspen-conifer communities in British Columbia. [26] Western tanagers' preference for multistoried habitats in the Black Hills may be related to the bur oak and quaking aspen/paper birch midstory. [29] Western tanagers were not significantly related with abundance of pineland dwarf mistletoe (Arceuthobium vaginatum ssp. cryptopodum) in ponderosa pine stands in central Colorado. The western tanager species was negatively associated with subalpine fir (A. lasiocarpa) cover in northern Rocky Mountain conifer forests. [30]

Food and feeding

Western tanagers obtain their food by foliage gleaning and hawking. [10] [11] [12] The degree to which each of these methods is used apparently varies across locations. For instance, in a California mixed conifer-oak forest consisting mainly of white fir, Douglas fir, incense-cedar, and California black oak, about 47% of western tanager foraging observations were gleaning, about 40% were hawking, and lunging and hovering occurred in about 6% and 7% of observations, respectively. [24] In contrast, in the mainly Douglas fir-dominated communities of interior British Columbia, gleaning constituted 93.2% of western tanager foraging observations. Hawking only occurred in 3.7% of observations and hovering in 3.1%. [25]

Western tanagers primarily glean from foliage. In the mixed conifer-oak woodland of California, 45% of their foraging observations were foliage gleaning. Western tanagers gleaned from twigs in 10% of observations and from branches in 5% of observations. Hawking constituted the remainder of western tanager foraging observations. [24] In British Columbia, 88.3% of gleaning observations occurred on foliage, 10.5% on branches and twigs, and 1.2% on trunks. [25]

Western tanagers eat fruits (~18%) and a wide range of insects (~82%). [10] Fruits include hawthorn apples (Crataegus spp.), raspberries (Rubus spp.), mulberries (Morus spp.), elderberries (Sambucus spp.), serviceberries (Amelanchier spp.), and wild and cultivated cherries (Prunus spp.). [11] [12] They have been observed foraging on Perry's agave (Agave parryi) nectar. Reports of western tanager eating eucalyptus (Eucalyptus spp.) nectar, Russian olive fruits, and human-provided food, including bird seed and dried fruit, were summarized. [11] Western tanagers are major consumers of western spruce budworms (Choristoneura occidentalis), [21] and they have been observed eating Douglas fir tussock moth larvae (Orgyia pseudotsugata). Hymenopterans, mostly wasps and ants, constituted 75% of insects in western tanager stomachs in August. The other insects were beetles (Coleoptera, 12%), mainly click beetles (Elateridae) and woodborers (Bupestridae), true bugs (Hemiptera, 8%), grasshoppers (Orthoptera, 4%), and caterpillars (Lepidoptera, 2%). [11] [12]

Predators

Several birds prey on western tanagers. Remains of a western tanager were found in a red-tailed hawk's (Buteo jamaicensis) nest in Colorado. [31] In southwestern Idaho, western tanager remains were reported in one of over 170 prairie falcon (Falco mexicanus) nests observed. Northern goshawks (Accipiter gentilis), Mexican spotted owls (Strix occidentalis spp. lucida), sharp-shinned hawks (A. striatus) and Cooper's hawks (A. cooperii) are also western tanager predators. [11] Accipiter hawks (Accipitrinae) and jays (Corvidae) are major predators of western tanagers. Domestic cats also preyed on western tanagers in British Columbia. [11]

Clark's nutcrackers (Nucifraga columbiana), northern pygmy owls (Glaucidium gnoma), great horned owls (Bubo virginianus), and jays such as scrub jays (Aphelocoma species), pinyon jays (Gymnorhinus cyanocephalus), and Steller's jays (Cyanocitta stelleri) are typical avian predators of western tanager nests. Other reported nest predators include black bears (Ursus americanus), prairie rattlesnakes (Crotalus viridis), and bullsnakes (Pituophis catenifer). [11]

Western tanager nests are parasitized by brown-headed cowbirds (Molothrus aster). [17] [32] Parasitism rates can be high, and can dramatically reduce the number of western tanagers fledged per nest. [11] [17]

Related Research Articles

<span class="mw-page-title-main">Douglas fir</span> Species of tree

The Douglas fir is an evergreen conifer species in the pine family, Pinaceae. It is native to western North America and is also known as Douglas-fir, Douglas spruce, Oregon pine, and Columbian pine. There are three varieties: coast Douglas-fir, Rocky Mountain Douglas-fir and Mexican Douglas-fir.

<i>Pseudotsuga menziesii <span style="font-style:normal;">var.</span> glauca</i> Variety of plants

Pseudotsuga menziesii var. glauca, or Rocky Mountain Douglas-fir, is an evergreen conifer native to the interior mountainous regions of western North America, from central British Columbia and southwest Alberta in Canada southward through the United States to the far north of Mexico. The range is continuous in the northern Rocky Mountains south to eastern Washington, eastern Oregon, Idaho, western and south-central Montana and western Wyoming, but becomes discontinuous further south, confined to "sky islands" on the higher mountains in Utah, Colorado, Arizona and New Mexico, with only very isolated small populations in eastern Nevada, westernmost Texas, and northern Mexico. It occurs from 600 m altitude in the north of the range, up to 3,000 m, rarely 3,200 m, in the south. Further west towards the Pacific coast, it is replaced by the related coast Douglas-fir, and to the south, it is replaced by Mexican Douglas-fir in high mountains as far south as Oaxaca. Some botanists have grouped Mexican Douglas-fir with P. menziesii var. glauca, but genetic and morphological evidence suggest that Mexican populations should be considered a different variety.

<i>Quercus kelloggii</i> Species of oak tree

Quercus kelloggii, the California black oak or Kellogg oak, is an oak in the red oak section native to western North America. Although genetically separated from them for more than 20 million years, its leaves are remarkably similar in appearance to several other members of the red oak section including the red oak and the black oak found in eastern and central North America.

<span class="mw-page-title-main">Olive warbler</span> Species of bird

The olive warbler is a small passerine bird. It is the only member of the genus Peucedramus and the family Peucedramidae.

<span class="mw-page-title-main">Eastern towhee</span> Species of bird

The eastern towhee is a large New World sparrow. The taxonomy of the towhees has been under debate in recent decades, and formerly this bird and the spotted towhee were considered a single species, the rufous-sided towhee.

<i>Pinus strobiformis</i> Species of conifer

Pinus strobiformis, commonly known as southwestern white pine, Mexican white pine or Chihuahua white pine, is a medium-sized white pine tree whose native habitat is in southwestern United States and Mexico. It is typically a high-elevation pine growing mixed with other conifers.

<i>Pinus ponderosa</i> Species of large pine tree in North America

Pinus ponderosa, commonly known as the ponderosa pine, bull pine, blackjack pine, western yellow-pine, or filipinus pine is a very large pine tree species of variable habitat native to mountainous regions of western North America. It is the most widely distributed pine species in North America.

<i>Abies concolor</i> Species of conifer tree

Abies concolor, the white fir, concolor fir, or Colorado fir, is a coniferous tree in the pine family Pinaceae. This tree is native to the mountains of western North America, including the Cascade Range and southern Rocky Mountains, and into the isolated mountain ranges of southern Arizona, New Mexico, and Northern Mexico. It naturally occurs at elevations between 900 and 3,400 metres.

<span class="mw-page-title-main">Marbled murrelet</span> Species of bird

The marbled murrelet is a small seabird from the North Pacific. It is a member of the family Alcidae, which includes auklets, guillemots, murres and puffins. It nests in old-growth forests or on the ground at higher latitudes where trees cannot grow. The marbled murrelet has declined in number since humans began logging its nest trees in the latter half of the 19th century. The decline of the marbled murrelet and its association with old-growth forests, at least in the southern part of its range, have made it a flagship species in the forest preservation movement.

<span class="mw-page-title-main">Abert's squirrel</span> Species of rodent

Abert's squirrel or the tassel-eared squirrel is a tree squirrel in the genus Sciurus native to the southern Rocky Mountains from the United States to the northern Sierra Madre Occidental of Mexico, with concentrations found in Arizona, New Mexico, and southwestern Colorado. It is closely associated with, and largely confined to, mature ponderosa pine forests. It is named in honor of the American naturalist John James Abert; nine subspecies are recognised. It is recognizable by its tufted ears, gray color, pale underparts and rufous patch on the lower back. The squirrel feeds on the seeds and cones of the Mexican pinyon and the ponderosa pine when they are available, but will also take fungi, buds, bark, and carrion. Breeding normally occurs in summer, with a spherical nest being built high in the canopy.

<span class="mw-page-title-main">Flame-colored tanager</span> Species of bird

The flame-colored tanager, formerly known as the stripe-backed tanager, is a medium-sized American songbird in the family Cardinalidae, the cardinals or cardinal grosbeaks. It is found from Mexico throughout Central America to northern Panama and occasionally in the United States; four subspecies are recognized. The flame-colored tanager is 18 to 19 cm long, the male having predominantly red-orange while the female is more yellowish orange.

<span class="mw-page-title-main">Red-headed tanager</span> Species of bird

The red-headed tanager is a medium-sized American songbird in the family Cardinalidae, the cardinals or cardinal grosbeaks. It is endemic to Mexico. The red-headed tanager is around 15 cm (5.9 in) long, the male has predominantly yellow-olive plumage with a red head and throat, while the female has a yellowish forecrown.

<span class="mw-page-title-main">White-winged tanager</span> Species of bird


The white-winged tanager is a medium-sized American songbird in the family Cardinalidae, the cardinals or cardinal grosbeaks. It is found from Mexico, through Central America, across northern South America and as far south as Bolivia.

<span class="mw-page-title-main">Rose-throated tanager</span> Species of bird

The rose-throated tanager is a medium-sized songbird in the family Cardinalidae, the cardinals or cardinal grosbeaks. Endemic to the Yucatán Peninsula in Central America, it is found in Belize, Guatemala, and Mexico. The male has greyish plumage with a deep rose throat and crown, while the female is similar but for a yellow crown and throat.

<span class="mw-page-title-main">Rocky Mountain ponderosa pine forest</span>

The Rocky Mountain ponderosa pine forest is a forest plant community at an elevation of 2,000–2,700 metres (6,600–8,900 ft) in the U.S. state of Colorado, depending on soil moisture. It is an important temperate coniferous forest ecoregion, including some endemic wildlife and grass species that are only found in this ponderosa pine habitat.

<span class="mw-page-title-main">Klamath Mountains (ecoregion)</span> Temperate coniferous forests ecoregion in northern California and southwestern Oregon

The Klamath Mountains ecoregion of Oregon and California lies inland and north of the Coast Range ecoregion, extending from the Umpqua River in the north to the Sacramento Valley in the south. It encompasses the highly dissected ridges, foothills, and valleys of the Klamath and Siskiyou Mountains. It corresponds to the Level III ecoregion designated by the Environmental Protection Agency and to the Klamath-Siskiyou forests ecoregion designated by the World Wide Fund for Nature.

The biogeoclimatic zones of British Columbia are units of a classification system used by the British Columbia Ministry of Forests for the Canadian province's fourteen different broad, climatic ecosystems. The classification system, termed Biogeoclimatic Ecosystem Classification, exists independently of other ecoregion systems, one created by the World Wildlife Fund and the other in use by Environment Canada, which is based on one created by the Commission for Environmental Cooperation (CEC) and also in use by the US Environmental Protection Agency (EPA). The system of biogeoclimatic ecosystem classification was partly created for the purpose of managing forestry resources, but is also in use by the British Columbia Ministry of Environment and Climate Change Strategy and other provincial agencies. A biogeoclimatic zone is defined as "a geographic area having similar patterns of energy flow, vegetation and soils as a result of a broadly homogenous macroclimate."

<span class="mw-page-title-main">Pinyon jay</span> Species of bird in North America

The pinyon jay is a species of jay, and is the only member of the genus Gymnorhinus. Native to Western North America, the species ranges from central Oregon to northern Baja California, and eastward as far as western Oklahoma, though wanderers are often sighted beyond this range. It is typically found within foothills, especially where pinyon pines occur.

<i>Pseudotsuga menziesii <span style="font-style:normal;">var.</span> menziesii</i> Variety of conifer

Pseudotsuga menziesii var. menziesii, commonly known as Coast Douglas-fir, Pacific Douglas-fir, Oregon pine, or Douglas spruce, is an evergreen conifer native to western North America from west-central British Columbia, Canada southward to central California, United States. In Oregon and Washington its range is continuous from the Cascades crest west to the Pacific Coast Ranges and Pacific Ocean. In California, it is found in the Klamath and California Coast Ranges as far south as the Santa Lucia Mountains with a small stand as far south as the Purisima Hills, Santa Barbara County. In the Sierra Nevada it ranges as far south as the Yosemite region. It occurs from near sea level along the coast to 1,800 metres (5,900 ft) in the California Mountains. Further inland, coast Douglas-fir is replaced by Rocky Mountain or interior Douglas-fir. Interior Douglas-fir intergrades with coast Douglas-fir in the Cascades of northern Washington and southern British Columbia.

<span class="mw-page-title-main">Ponderosa pine forest</span>

Ponderosa pine forest is a plant association and plant community dominated by ponderosa pine and found in western North America. It is found from the British Columbia to Durango, Mexico. In the south and east, ponderosa pine forest is the climax forest, while in the more northern part of its range, it can transition to Douglas-fir or grand fir, or white fir forests. Understory species depends on location. Fire suppression has led to insect outbreaks in ponderosa pine forests.

References

PD-icon.svg This article incorporates public domain material from Piranga ludoviciana. United States Department of Agriculture.

  1. BirdLife International (2016). "Piranga ludoviciana". IUCN Red List of Threatened Species . 2016: e.T22722471A94768218. doi: 10.2305/IUCN.UK.2016-3.RLTS.T22722471A94768218.en . Retrieved 12 November 2021.
  2. Wilson, Alexander (1811). American Ornithology; or, the Natural History of the Birds of the United States: Illustrated with Plates Engraved and Colored from Original drawings taken from Nature. Vol. 3. Philadelphia: Bradford and Inskeep. pp. 27–28, Plate 20 fig. 1.
  3. Davis, William B.; Stevenson, James (1934). "The type localities of three birds collected by Lewis and Clark in 1806". Condor. 36 (4): 161–163 [163]. doi: 10.2307/1363415 . JSTOR   1363415.
  4. Paynter, Raymond A. Jr, ed. (1970). Check-List of Birds of the World. Vol. 13. Cambridge, Massachusetts: Museum of Comparative Zoology. p. 307.
  5. Jobling, James A. (2010). The Helm Dictionary of Scientific Bird Names. London: Christopher Helm. p. 232. ISBN   978-1-4081-2501-4.
  6. Vieillot, Louis Pierre (1807). Histoire naturelle des oiseaux de l'Amérique Septentrionale : contenant un grand nombre d'espèces décrites ou figurées pour la première fois (in French). Vol. 1. Paris: Chez Desray. p. iv. Dickinson, E.C.; Overstreet, L.K.; Dowsett, R.J.; Bruce, M.D. (2011). Priority! The Dating of Scientific Names in Ornithology: a Directory to the literature and its reviewers. Northampton, UK: Aves Press. p. 157. ISBN   978-0-9568611-1-5.
  7. 1 2 Gill, Frank; Donsker, David; Rasmussen, Pamela, eds. (2020). "Cardinals, grosbeaks and (tanager) allies". IOC World Bird List Version 10.2. International Ornithologists' Union. Retrieved 1 October 2020.
  8. 1 2 "Western Tanager Identification, All About Birds, Cornell Lab of Ornithology". www.allaboutbirds.org. Retrieved 2020-09-30.
  9. "nps.gov - Western Tanager" (PDF).
  10. 1 2 3 4 5 6 DeGraaf, Richard M.; Scott, Virgil E.; Hamre, R. H. et al. (1991) Forest and rangeland birds of the United States: Natural history and habitat use. Agric. Handb. 688. Washington, DC: U.S. Department of Agriculture, Forest Service
  11. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 Hudon, Jocelyn. 1999. Western tanager—Piranga ludoviciana. In: Poole, A.; Gill, F., eds. The birds of North America. No. 432. Ithaca, NY: Cornell Laboratory of Ornithology; Philadelphia, PA: The Academy of Natural Sciences
  12. 1 2 3 4 5 6 7 8 9 10 11 12 Isler, Morton L.; Isler, Phyllis R. 1987. The tanagers: Natural history, distribution, and identification. Washington, DC: Smithsonian Institution Press
  13. Veit, Richard R. (2000). "Vagrants as the Expanding Fringe of a Growing Population". The Auk. 117 (1): 242–246. doi: 10.1642/0004-8038(2000)117[0242:VATEFO]2.0.CO;2 . JSTOR   4089566. S2CID   85877746.
  14. 1 2 Hagar, Donald C. (1960). "The interrelationships of logging, birds, and timber regeneration in the Douglas-fir region of northwestern California". Ecology. 41 (1): 116–125. doi:10.2307/1931945. JSTOR   1931945.
  15. 1 2 3 4 5 6 Yong, Wang; Finch, Deborah M. 2002. Stopover ecology of landbirds migrating along the Middle Rio Grande in spring and fall. Gen. Tech. Rep. RMRS-GTR-99. Ogden, UT: U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station
  16. 1 2 Tatschl, John L. (1967). "Breeding birds of the Sandia Mountains and their ecological distributions". The Condor. 69 (5): 479–490. doi:10.2307/1366148. JSTOR   1366148.
  17. 1 2 3 4 5 6 7 8 9 10 Fischer, Karen N.; Prather, John W.; Cruz, Alexander (2002). "Nest site characteristics and reproductive success of the western tanager (Piranga ludoviciana) on the Colorado Front Range". Western North American Naturalist. 62 (4): 479–483.
  18. Klimkiewicz, M. Kathleen; Futcher, Anthony G. (1987). "Longevity records of North American birds: Coerebinae through Estrildidae" (PDF). Journal of Field Ornithology. 58 (3): 318–333.
  19. 1 2 Stiles, Edmund W. (1980). "Bird community structure in alder forests in Washington". The Condor. 82 (1): 20–30. doi:10.2307/1366781. JSTOR   1366781.
  20. Medin, Dean E.; Welch, Bruce L.; Clary, Warren P. 2000. Bird habitat relationships along a Great Basin elevational gradient. Res. Pap. RMRS-RP-23. Fort Collins, CO: U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station
  21. 1 2 3 4 5 Langelier, Lisa A.; Garton, Edward O. 1986. Spruce budworms handbook: Management guidelines for increasing populations of birds that feed on western spruce budworm. Agriculture Handbook No. 653. Washington, DC: U.S. Department of Agriculture, Forest Service, Cooperative State Research Service
  22. 1 2 Meslow, E. Charles; Wight, Howard M. 1975. Avifauna and succession in Douglas-fir forests of the Pacific Northwest. In: Smith, Dixie R, technical coordinator. Proceedings of the symposium on management of forest and range habitats for nongame birds; 1975 May 6–9; Tucson, AZ. Gen. Tech. Rep. WO-1. Washington, DC: U.S. Department of Agriculture, Forest Service: 266–271
  23. 1 2 Kilgore, Bruce M. (1971). "Response of breeding bird populations to habitat changes in a giant sequoia forest". The American Midland Naturalist. 85 (1): 135–152. doi:10.2307/2423918. JSTOR   2423918.
  24. 1 2 3 4 Airola, Daniel A.; Barrett, Reginald H. (1985). "Foraging and habitat relationships of insect-gleaning birds in a Sierra Nevada mixed-conifer forest". The Condor. 87 (2): 205–216. doi:10.2307/1366884. JSTOR   1366884.
  25. 1 2 3 4 5 Morgan, K. H.; Savard, J-P. L.; Wetmore, S. P. (1991) Foraging behaviour of forest birds of the dry interior Douglas-fir, ponderosa pine forests of British Columbia. Technical Report Series No. 149. Delta, BC: Canadian Wildlife Service, Pacific and Yukon Region
  26. 1 2 Pojar, Rosamund A. 1995. Breeding bird communities in aspen forests of the sub-boreal spruce (dk subzone) in the Prince Rupert Forest Region. Land Management Handbook No. 33. Victoria, BC: Province of British Columbia, Ministry of Forests Research Program
  27. 1 2 Schieck, Jim; Nietfeld, Marie. 1995. Bird species richness and abundance in relation to stand age and structure in aspen mixedwood forests in Alberta. In: Stelfox, J. B., ed. Relationships between stand age, stand structure, and biodiversity in aspen mixedwood forests in Alberta. Vegreville, AB: Alberta Environmental Centre: 115–157
  28. 1 2 Zwartjes, Patrick W.; Cartron, Jean-Luc E.; Stoleson, Pamela L. L.; Haussamen, Walter C.; Crane, Tiffany E. 2005. Assessment of native species and ungulate grazing in the Southwest: terrestrial wildlife. Gen. Tech. Rep. RMRS-GTR-142. Fort Collins, CO: U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station
  29. 1 2 3 Mills, Todd R.; Rumble, Mark A.; Flake, Lester D. (2000). "Habitat of birds in ponderosa pine and aspen/birch forest in the Black Hills, South Dakota". Journal of Field Ornithology. 71 (2): 187–206. doi:10.1648/0273-8570-71.2.187. S2CID   86086800.
  30. Hutto, Richard L. (1995). "Composition of bird communities following stand-replacement fires in northern Rocky Mountain (U.S.A.) conifer forests". Conservation Biology. 9 (5): 1041–1058. doi:10.1046/j.1523-1739.1995.9051033.x-i1. JSTOR   2387043. PMID   34261259.
  31. Blumstein, Daniel T. (1989). "Food habits of red-tailed hawks in Boulder County, Colorado". Journal of Raptor Research. 23 (2): 53–55.
  32. Goguen, Christopher B.; Mathews, Nancy E. (1998). "Songbird community composition and nesting success in grazed and ungrazed pinyon-juniper woodlands" (PDF). Journal of Wildlife Management. 62 (2): 474–484. doi:10.2307/3802321. JSTOR   380232.