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Adult western tanagers are unlikely to suffer directly from fire. It is generally accepted that large, fast-moving fires can result in mortality, but adult birds typically have the mobility to avoid fire [26,30,73].
It is likely that nests are more vulnerable to fire [30,92]. Although there were no data directly investigating western tanager nest mortality due to fire as of 2006, literature reviews have used fire characteristics and life history of species to speculate on possible effects of fire on nesting success and bird populations [73,102]. Due to the height of most western tanager nests (see Nesting habitat), only relatively severe fires would directly impact their young. Since conditions necessary for fire severe enough to affect nests higher in the canopy typically occur after nesting season [73], it is likely that direct effects of growing-season fire on western tanager nests would be uncommon compared to species nesting lower to the ground. In addition, the possibility of western tanager renesting may reduce the direct effects of a fire on western tanager recruitment [73,102]. Nests impacted early enough in the breeding season could be compensated for by later nesting attempts. However, since western tanagers only rear 1 brood per season (see Timing of Major Life History Events) fires of enough severity in the mid- to late-breeding season are likely to have a larger effect on western tanagers than fires before or after the breeding season [72] and may have substantial impacts on the survival of western tanager nestlings and fledglings. In addition to fire severity and timing, other fire characteristics such as the uniformity of the burn and fire frequency are likely to influence the degree to which fire directly impacts western tanager reproduction [52,73].
The breeding range of the western tanager, as described by literature reviews and field guides, includes forests along the western coast of North America from southeastern Alaska south to northern Baja California. 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 [28,54,58,117]. Reviews report the western tanager's wintering range as stretching 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 [28,54,58,117]. Accidentals are rare to casual in the eastern United States [117,129]. A general map of the western tanager's distribution can be found at Cornell's All About Birds website.
The following lists are speculative and are based on western tanager distribution information and the habitat characteristics and species composition of communities western tanagers are known to occupy during migration and breeding. There is not conclusive evidence that western tanagers occur in all the habitat types listed and some community types, especially nonconiferous habitats, may have been omitted. Abundance of western tanagers in the community types listed is variable. Western tanagers are rarely observed in some of the following communities and are quite common in others. See Preferred Habitat for more detail.
According to several reviews, western tanager obtain their food by foliage gleaning and hawking [28,54,58]. 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, while lunging and hovering occurred in about 6% and 7% of observations, respectively [2]. In contrast, in the mainly Douglas-fir dominated communities of interior British Columbia, gleaning comprised 93.2% of western tanager foraging observations. Hawking only occurred in 3.7% of observations and hovering in 3.1% [88].
Western tanagers primarily glean from foliage. In the mixed conifer-oak woodland of California, 45% of western tanager foraging observations were foliage gleaning. Western tanagers gleaned from twigs in 10% of observations and from branches in 5% of observations. Hawking comprised the remainder of western tanager foraging observations [2]. In British Columbia, 88.3% of gleaning observations occurred on foliage, 10.5% on branches and twigs, and 1.2% on trunks [88].
Western tanagers eat fruits and a wide range of insects. A field guide states that western tanager's diet is about 18% plant matter and 82% insects [28]. According to a literature review, fruits eaten by western tanagers include hawthorn apples (Crataegus spp.), raspberries (Rubus spp.), mulberries (Morus spp.), elderberries (Sambucus spp.), serviceberries (Amelanchier spp.), and wild and cultivated cherries (Prunus spp.) [54,58,75]. Western tanagers have been observed foraging on Perry's agave (Agave parryi) nectar [65]. Reports of western tanager eating Eucalyptus (Eucalyptus spp.) nectar, Russian-olive fruits, and human-provided food, including bird seed and dried fruit, were summarized in a review [54]. A literature review asserts that western tanagers are major consumers of western spruce budworms (Choristoneura occidentalis) [66], and they have been observed eating Douglas-fir tussock moth larvae (Orgyia pseudotsugata) [127]. A study summarized in literature reviews [54,58] found 75% of insects in western tanager stomachs in August were Hymenopterans, mostly wasps and ants. The other insects observed were beetles (Coleoptera,12%), mainly click beetles (Elateridae) and woodborers (Bupestridae), true bugs (Hemipterans, 8%), grasshoppers (Orthoptera, 4%) and caterpillars (Lepidoptera, 2%).
Despite several articles that discuss the effect of fire on western tanagers, results should be interpreted with caution. As noted by a literature review summarizing songbird responses to fire in southwestern ponderosa pine forests [34], there are several limitations to many studies addressing bird response to fire. Most studies are restricted in spatial or temporal scale. Many are opportunistic, include confounding factors, and/or lack sufficient replication. There is also a lack of studies that compare demographic parameters of western tanager between burned and unburned vegetation, which is necessary to determine if a site is meeting the needs of western tanagers [34].
Reviews that address the effect of fire on western tanager demonstrate that several different responses have been observed [47,63,108]. However, it is possible that fire severity explains a considerable portion of the observed variation. It appears that western tanagers generally respond positively to low-severity fire and negatively to high- severity fire.
Western tanager abundance has been observed to increase after low- to moderate-severity fire [19,21,116]. Western tanager was significantly (p<0.05) more abundant in the year after prescribed underburns in a ponderosa pine forest and pine-grassland ecotone of Wind Cave National Park, South Dakota compared to unburned sites [21]. Abundance of western tanager was much greater (103 detections) on a site moderately affected by wildfire in ponderosa pine forests in Arizona than on an unburned site (20 detections) [19]. In low- to mid-elevation conifer communities of western Montana, western tanagers were significantly (p=0.005) more abundant after wildfire resulted in <20% tree mortality than before the wildfire occurred. Western tanager abundance did not increase significantly (p>0.05) on sites subject to moderate (20%-80% tree mortality) wildfire. The differences ((after fire mean minus before fire mean) x 100) in western tanagers detected before and after fire at unburned points and points that burned at low (<20% tree mortality), moderate (20%-80% tree mortality) or high severity (>80% tree mortality) are shown in the table below (sx is in parentheses) [116].
Unburned (n=120) Low (n=52) Moderate (n=32) Severe (n=38) after fire mean - before fire mean 2.4 (5.2) 23.9 (7.3) 12.1 (8.9) -15.4 (8.6)Much of the evidence for decreases in western tanager abundance comes from investigations of high- severity fires. In coniferous forests of Yellowstone and Grand Teton National Parks, western tanagers occurred at higher densities on unburned sites (up to 15 western tanagers/100 acres) and moderately burned sites ≤3 years old (up to 10 western tanagers/100 acres) than in areas that had burned in severe fires 2 and 3 years previously, where western tanagers were only observed outside of transects [125]. In the Sierra Nevada of California, western tanager occurred at higher densities in unburned (0.75-1.5 pairs/plot) mixed-coniferous vegetation dominated by Jeffrey pine and white fir than on sites that burned in the stand-replacing Donner Ridge Fire 6 to 8 years earlier (0-0.25 pair/plot). The burned sites were comprised of small pockets of Jeffrey pine and white fir along with post-fire vegetation such as woolly mule-ears (Wyethia >mollis), golden current (Ribes aureum), and greenleaf manzanita (Arctostaphylos patula) [20]. The trend on this site continued through 1985, with western tanager occurring at a density of 0.2 territory/plot in the burned area 15 years after the fire and 1.7 territories/plot in unburned vegetation dominated by Jeffrey pine, ponderosa pine, Washoe pine (P. washoensis), their intermediates, and white fir [98]. Although the response was not significant (p>0.05), western tanager abundance declined after severe (>80% tree mortality) wildfire in coniferous forests on low- to mid-elevation sites in western Montana [116]. A literature review that summarized the findings of 11 published and unpublished studies reported that western tanagers were more abundant on unburned sites than on 23 severely-burned conifer forest sites [63].
Studies incorporating a range of fire severities have found fire resulted in no change in western tanager abundance. For instance, in ponderosa pine-dominated forests in northern Arizona and New Mexico, western tanager did not respond to low to moderate severity prescribed burns and wildfire. The average western tanager detections over the 4 years before a prescribed burn (2.75) in Arizona were similar to the year after the fire (3.00). Average western tanager detections before a wildfire (16) on a New Mexico site were not substantially different from detections in the 2 years after the burn (13.5) [16]. Western tanagers response to high-severity surface fires in white fir and red fir communities of Yosemite National Park were inconclusive [42]. In ponderosa pine forests in Arizona, 24 western tanagers were detected on sites 3 years after they were severely burned, while 20 were detected on an adjacent unburned site [19].
Habitat type is likely to influence western tanager's response to fire. Since western tanagers appear to occur at relatively low abundance in dense forests [12,38,51] and are generally rare on very open sites such as clearcuts [25,49,128], sagebrush communities, and grasslands [57], fires that reduce tree density without dropping below some threshold may favor western tanagers. In pinyon-juniper communities of east-central Nevada, western tanagers were more abundant on a prescribed burn site than an unburned site before the burn, but were absent on the prescribed burn site after burning. In this habitat, burned areas were mainly low and herbaceous, while unburned areas were multi-layered and woody [76,77]. In addition, different western tanager responses to wildfire in different communities were reported in Grand Teton National Park. Western tanager was more abundant during the breeding season on a riparian-coniferous forest ecotone where the forest had burned in a wildfire 2 years previously than on a similar ecotone site that had not burned. However, in a sagebrush-coniferous forest ecotone western tanager breeding season abundance was greater on the unburned site than the site where the forest had burned 2 years previously [115]. According to a literature review, western tanagers occur more often in unburned than severely burned ponderosa pine forest, but are more common after stand-replacing fires in lodgepole pine communities than dense lodgepole pine forest [63].
Several factors including time since burn, occurrence of salvage logging, and fire characteristics such as size, frequency, uniformity, and season of burn are likely to influence western tanager response. However, little data are available on these factors and the type, size, and duration of their impacts on western tanager are largely unknown.
The effect of time since burn is uncertain. Nesting requirements (see Nesting habitat) suggest that extensive severe fire could result in long-term declines in western tanagers, due to the time required for large trees to regenerate on a site. However, a literature review found a higher percentage of studies reporting western tanager in early-successional burned forest (83%) than in mid-successional burned forest (20%) [56].
Salvage logging may also affect western tanagers response. In western Montana coniferous forests, western tanager density was the same in a burned forest salvaged logged to a density of 855 trees/ha, as in the unlogged burned forest with a tree density of 970/ha. However, western tanager did not occur on a salvage-logged site where a 70-ha clearcut and a 70-ha thinning to 125 trees/ha were performed after fire, while an average of 4.0 western tanagers/40 ha were observed on the burn site that was not logged (1,043 trees/ha) [50].
Given the possible importance of spatial arrangement of habitat (see Effects of spatial arrangement/area), the size and patchiness of a burn may also influence western tanager's response to fire. A literature review notes that many species that had mixed responses to fire, which included western tanager, occurred at their highest abundances within 165 feet (50 m) of the edge of burns [63]. In western Montana and northern Wyoming western tanager was negatively associated with size of stand-replacing fire, although the relationship was not significant (p>0.05) [56]. The relationship of fire to several aspects of habitat configuration is discussed in a review of the effects of fire at landscape scales [71].
Season of the burn may also affect western tanager's response. Although western tanager abundance was uniformly low in a mountain big sagebrush ecosystem (Artemisia tridentata var. vaseyana) of Wyoming, the greatest number of detections occurred in the second year following a spring prescribed burn, compared to fall prescribed burn and unburned sites [79]. Since western tanagers appear to prefer moderate to open forest stands (see Stand structure/composition), the fire frequency may affect western tanagers by influencing fire severity and forest structure [55] .
Very little information is available on the effect fire has on western tanager food resources. Although food available from gleaning foliage is likely to decline due to fire, it has been suggested that western tanager may be able to mitigate at least some of this loss by hawking aerial insects. However, little is known of these insects' response to fire [42]. General information on plant food response to fire can be found in [13,70]
Fire ecology: Western tanagers occur in a variety of habitats with a wide range of FIRE REGIMES. Breeding is most common in coniferous forests, which have FIRE REGIMES that range from frequent low-severity surface fires [18] to infrequent stand-replacement fires. A literature review provides a general overview of FIRE REGIMES in western coniferous forests [63].
FIRE REGIMES: The following table provides fire return intervals for plant communities and ecosystems where western tanager is important. Find fire regime information for the plant communities in which this species may occur by entering the species name in the FEIS home page under "Find FIRE REGIMES".
Community or ecosystem Dominant species Fire return interval range (years) silver fir-Douglas-fir Abies amabilis-Pseudotsuga menziesii var. menziesii >200 grand fir Abies grandis 35-200 [6] sagebrush steppe Artemisia tridentata/Pseudoroegneria spicata 20-70 [93] mountain big sagebrush Artemisia tridentata var. vaseyana 15-40 [7,23,85] coastal sagebrush Artemisia californica <35 to <100 [93] saltbush-greasewood Atriplex confertifolia-Sarcobatus vermiculatus <35 to >100 [93,137] California montane chaparral Ceanothus and/or Arctostaphylos spp. 50-100 [93] mountain-mahogany-Gambel oak scrub Cercocarpus ledifolius-Quercus gambelii <35 to <100 blackbrush Coleogyne ramosissima <35 to <100 western juniper Juniperus occidentalis 20-70 Rocky Mountain juniper Juniperus scopulorum <35 creosotebush Larrea tridentata <35 to <100 [93] Engelmann spruce-subalpine fir Picea engelmannii-Abies lasiocarpa 35 to >200 [6] black spruce Picea mariana 35-200 [31] blue spruce* Picea pungens 35-200 [6] pinyon-juniper Pinus-Juniperus spp. <35 [93] whitebark pine* Pinus albicaulis 50-200 [1,4] Mexican pinyon Pinus cembroides 20-70 [87,121] Rocky Mountain lodgepole pine* Pinus contorta var. latifolia 25-340 [10,11,123] Sierra lodgepole pine* Pinus contorta var. murrayana 35-200 [6] Colorado pinyon Pinus edulis 10-400+ [37,41,59,93] Jeffrey pine Pinus jeffreyi 5-30 [6] western white pine* Pinus monticola 50-200 [6] Pacific ponderosa pine* Pinus ponderosa var. ponderosa 1-47 [6] interior ponderosa pine* Pinus ponderosa var. scopulorum 2-30 [6,9,68] Arizona pine Pinus ponderosa var. arizonica 2-15 [9,27,113] galleta-threeawn shrubsteppe Pleuraphis jamesii-Aristida purpurea <35 to <100 [93] quaking aspen-paper birch Populus tremuloides-Betula papyrifera 35-200 [31,131] quaking aspen (west of the Great Plains) Populus tremuloides 7-120 [6,44,83] mesquite Prosopis glandulosa <35 to <100 [80,93] mountain grasslands Pseudoroegneria spicata 3-40 ( x=10) [5,6] Rocky Mountain Douglas-fir* Pseudotsuga menziesii var. glauca 25-100 [6,7,8] coastal Douglas-fir* Pseudotsuga menziesii var. menziesii 40-240 [6,90,101] California mixed evergreen Pseudotsuga menziesii var. menziesii-Lithocarpus densiflorus-Arbutus menziesii <35 [6] California oakwoods Quercus spp. <35 [6] oak-juniper woodland (Southwest) Quercus-Juniperus spp. <35 to <200 [93] coast live oak Quercus agrifolia 2-75 [43] canyon live oak Quercus chrysolepis <35 to 200 [6] blue oak-foothills pine Quercus douglasii-P. sabiniana <35 [6] Oregon white oak Quercus garryana <35 [6] California black oak Quercus kelloggii 5-30 [93] interior live oak Quercus wislizenii <35 [6] redwood Sequoia sempervirens 5-200 [6,35,120] western redcedar-western hemlock Thuja plicata-Tsuga heterophylla >200 [6] western hemlock-Sitka spruce Tsuga heterophylla-Picea sitchensis >200 [6] mountain hemlock* Tsuga mertensiana 35 to >200 [6] *fire return interval varies widely; trends in variation are noted in the species reviewSeveral birds prey on western tanagers. Remains of a western tanager were found in a red-tailed hawk's (Buteo jamaicensis) nest in Colorado [17]. In southwestern Idaho, western tanager remains were reported in 1 of over 170 prairie falcon (Falco mexicanus) nests observed [91]. According to literature reviews, 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 [54,100,132]. One review asserts that accipiter hawks (Accipitrinae) and jays (Corvidae) are the major predators of western tanagers. This review also includes a report of a domestic cat (Felis catus) preying on a female western tanager in British Columbia [54].
According to literature reviews, Clark's nutcrackers (Nucifraga columbiana), northern pygmy-owls (Glaucidium gnoma), great horned owls (Bubo virginianus), and jays such as scrub jays (Aphelocoma spp.), 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) [54]
Western tanager nests are parasitized by brown-headed cowbirds (Molothrus aster) [36,40]. Parasitism rates can be high [40], and parasitism has been shown to dramatically reduce the number of western tanagers fledged per nest [36]. A literature review summarizes information related to western tanager nest parasitism [54].
BEHAVIOR:A literature review provides a detailed summary of migration and other behaviors such as vocalizations, territoriality, and self-maintenance [54].
Western tanagers arrive on their breeding grounds (see General Distribution) in spring. Literature reviews report breeding primarily by western tanagers that are ≥2 years old beginning in May and continuing into July, although some 1st-year western tanagers also breed [54,58]. In the Sandia Mountains of north-central New Mexico, western tanagers were heard singing beginning in late May, and the 1st nest was found in early June [124]. 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 [36]. A review [54] summarizes records of brooding dates in several areas of the West. 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 [54].
According to reviews, cup nests are built by the female, take about 4 or more days to construct, and are made from twigs, rootlets, grasses, and pine needles [54,58]. There is no evidence for 2nd broods in western tanagers [36,54]. However, a literature 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 [54]. In addition, renesting was suggested as the explanation for a few late nests observed in Boulder County, Colorado [36].
Clutch size is typically 3 to 5 eggs [36,54,58]. Average clutch size in 10 nonparasitized nests in Boulder County was 3.8 eggs [36]. A literature review suggests that average clutch in the Southwest may be smaller than that of western tanagers nesting in the North [54]. According to a personal communication cited in a literature review, egg laying generally takes about 1 day per egg [54]. The female incubates the eggs for approximately 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 [36,54,58]. According to a literature review, immature western tanagers have been observed with the parents at least 2 weeks after fledging [54].
A literature review notes that 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 [54].
Reproductive success of western tanagers varies widely between studies and across years. A summary of nest success in a literature review included an average annual nest success probability estimate of 0.186 over 3 years, with a low of 0.035 and a high of 0.349 [54]. In a northern Arizona study area, an average of 43% (n=7) of nests succeeded to the nestling stage [16]. In Boulder County, nesting success varied from 11.3% to 75.3%, with an average of 51.8% over a 3-year period [36]. 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 [40]. According to a review, 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 [54].
Western tanagers can live several years. A literature review includes an estimate of annual average survival rate of 0.753 and a return rate of 30.1% for western tanagers in west-central Idaho [54]. A wild western tanager 7 years and 11 months old has been documented from banding data [61].
Given the available data (see HABITAT RELATED FIRE EFFECTS) and the nesting (Nesting habitat) and foraging (Foraging habitat) requirements of western tanagers, it is likely that western tanagers will tend to increase after low- to moderate-severity fires and tend to decline after high-severity fires. Much more research is necessary, including investigations addressing the effect of fire characteristics, habitat type, and time since fire on western tanager demographics and the effects of fire on western tanager prey.
Fire's effect on abundance of predators and parasites [13] should also be considered when considering the impact of fire in potential or occupied western tanager habitat.
Distribucion General: Se reproduce en el oeste de América del Norte hacia el sur, hasta el norte de Baja California. Invierna desde la parte central de México hasta Costa Rica. Llega en forma casual a Panamá.
Les especies d'aves con nome común en llingua asturiana márquense como NOA. En casu contrariu, conséñase'l nome científicu o de la SEO.
'''Piranga ludoviciana ees una especie d'ave paseriforme de la familia Cardinalidae (anque delles fontes asitien el so xéneru, Piranga en Thraupidae). Añera nel oeste de Norteamérica y invierna nel sur de Méxicu y América Central.
Cuando lleguen a la edá adulta, miden ente 15 y 19 cm de llargor. El machu ye de cabeza colorada, tornándose amarellentáu na parte posterior de la mesma. La nuca, el pechu, el banduyu y la rabadilla son mariellos. El llombu, la cola y les nales son negres, pero estes postreres presenten dos rayes blanques con mariellu. El picu ye amarellentáu bien claro y les pates negres.
La fema, al igual qu'otres especies cercanes (en particular P. rubra y P. olivacea) tien les partes dorsales verde oliva y les ventrales marielles, amás de tener el picu claru y les pates negres, pero estrémase porque, al igual que'l machu, tien dos rayes marielles con blancu nes nales, qu'amás presenten daqué de negru. Adicionalmente hai un esbozu de raya supraocular amarellentada.
Ye'l tráupido qu'añera más al norte, dende'l sur d'Alaska hasta l'estremu noroeste de Méxicu, principalmente en montes de coníferes y montes mistos. Constrúin un nial pocu compactu sobre una caña horizontal d'un árbol, xeneralmente una conífera. La fema pon cuatro güevos verdes azulosos con llurdios marrones.
Pel hibiernu migren escontra'l sur, y nesta estación distribúise dende'l sur de la península de Baxa California y el centru-occidente de Méxicu hasta Costa Rica, en tierres baxes, algamando númberos poblacionales altos.
Aliméntase d'inseutos y frutos. Suelen alimentase a lo cimero de los árboles, o bien prinden inseutos nel vuelu.
Esta páxina forma parte del wikiproyeutu Aves, un esfuerciu collaborativu col fin d'ameyorar y organizar tolos conteníos rellacionaos con esti tema. Visita la páxina d'alderique del proyeutu pa collaborar y facer entrugues o suxerencies. Les especies d'aves con nome común en llingua asturiana márquense como NOA. En casu contrariu, conséñase'l nome científicu o de la SEO. '''Piranga ludoviciana ees una especie d'ave paseriforme de la familia Cardinalidae (anque delles fontes asitien el so xéneru, Piranga en Thraupidae). Añera nel oeste de Norteamérica y invierna nel sur de Méxicu y América Central.
Cuando lleguen a la edá adulta, miden ente 15 y 19 cm de llargor. El machu ye de cabeza colorada, tornándose amarellentáu na parte posterior de la mesma. La nuca, el pechu, el banduyu y la rabadilla son mariellos. El llombu, la cola y les nales son negres, pero estes postreres presenten dos rayes blanques con mariellu. El picu ye amarellentáu bien claro y les pates negres.
La fema, al igual qu'otres especies cercanes (en particular P. rubra y P. olivacea) tien les partes dorsales verde oliva y les ventrales marielles, amás de tener el picu claru y les pates negres, pero estrémase porque, al igual que'l machu, tien dos rayes marielles con blancu nes nales, qu'amás presenten daqué de negru. Adicionalmente hai un esbozu de raya supraocular amarellentada.
Ye'l tráupido qu'añera más al norte, dende'l sur d'Alaska hasta l'estremu noroeste de Méxicu, principalmente en montes de coníferes y montes mistos. Constrúin un nial pocu compactu sobre una caña horizontal d'un árbol, xeneralmente una conífera. La fema pon cuatro güevos verdes azulosos con llurdios marrones.
Pel hibiernu migren escontra'l sur, y nesta estación distribúise dende'l sur de la península de Baxa California y el centru-occidente de Méxicu hasta Costa Rica, en tierres baxes, algamando númberos poblacionales altos.
Aliméntase d'inseutos y frutos. Suelen alimentase a lo cimero de los árboles, o bien prinden inseutos nel vuelu.
Piranga ludoviciana és una espècie d'ocell de la família Thraupidae que nia a l'oest d'Amèrica del Nord i hiverna al sud de Mèxic i Amèrica Central. Quan arriben a l'edat adulta, mesuren entre 15 i 19 cm de longitud. El mascle té el cap vermell per davant i més groguenc pel darrere. L'esquena, la cua i les ales són negres, però aquestes últimes presenten dues ratlles blanques amb groc. El bec és groguenc molt clar i les potes negres.
Aderyn a rhywogaeth o adar yw Tanagr y Gorllewin (sy'n enw gwrywaidd; enw lluosog: tanagrod y Gorllewin) a adnabyddir hefyd gyda'i enw gwyddonol Piranga ludoviciana; yr enw Saesneg arno yw Western tanager. Mae'n perthyn i deulu'r Breision (Lladin: Emberizidae) sydd yn urdd y Passeriformes.[1]
Talfyrir yr enw Lladin yn aml yn P. ludoviciana, sef enw'r rhywogaeth.[2] Mae'r rhywogaeth hon i'w chanfod yng Ngogledd America.
Mae'r tanagr y Gorllewin yn perthyn i deulu'r Breision (Lladin: Emberizidae). Dyma rai o aelodau eraill y teulu:
Rhestr Wicidata:
rhywogaeth enw tacson delwedd Bras Brewer Spizella breweri Bras coed Spizella arborea
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Aderyn a rhywogaeth o adar yw Tanagr y Gorllewin (sy'n enw gwrywaidd; enw lluosog: tanagrod y Gorllewin) a adnabyddir hefyd gyda'i enw gwyddonol Piranga ludoviciana; yr enw Saesneg arno yw Western tanager. Mae'n perthyn i deulu'r Breision (Lladin: Emberizidae) sydd yn urdd y Passeriformes.
Talfyrir yr enw Lladin yn aml yn P. ludoviciana, sef enw'r rhywogaeth. Mae'r rhywogaeth hon i'w chanfod yng Ngogledd America.
Die Kieferntangare (Piranga ludoviciana) ist ein kleiner Vogel aus der Familie der Kardinäle (Cardinalidae). Entdeckt wurde der Vogel von Meriwether Lewis und William Clark während der Lewis-und-Clark-Expedition im Westen von Louisiana. Deshalb bekam er am Anfang von Alexander Wilson auch den Namen „Louisianatangare“.
Das Kopfgefieder ist bei dem Männchen im Brutkleid leuchtend rot. Im Nacken, an der Brust und auf der Unterseite ist das Federkleid gelb. Auf den grauschwarzen bis schwarzen Flügeldecken befinden sich gelbe und weiße Flügelstäbe. Die Rückenseite, außer dem gelben Hinterbereich, und die Schwanzfedern sind ebenfalls schwarzgrau bis schwarz. Bei dem Weibchen ist das Kopfgefieder olivgrün bis gräulich und die Flügeldecken und Schwanzfedern haben eine mattere schwarzgraue Farbe. Der vordere Rückenbereich ist wie das Kopfgefieder olivgrün bis gräulich. Im Winter nimmt der Kopfbereich des Männchens eine gelbliche Farbe an.
Der rote Farbstoff im Gesicht der Kieferntangare ist Rhodoxanthin, ein bei Vögeln seltenes Pigment. Es wird nicht vom Vogel gebildet, wie bei anderen Tangaren, sondern aus der Nahrung, vermutlich durch Insekten, aufgenommen.[1]
Das Nest wird in den unteren Regionen von Tannen, Kiefern oder Fichten erbaut. Das Gelege besteht aus drei bis fünf hellblauen bis bläulichgrünen Eiern.
Sie ernähren sich überwiegend von Insekten. Gelegentlich werden auch Früchte verzehrt.[1] Ihre Beutetiere spüren sie meist in den oberen Regionen der Bäume auf
Gebrütet wird in der Regel in Mischwäldern in den Bergen. Das Verbreitungsgebiet erstreckt sich vom Nordwesten in Kanada über Nordwestamerika. Im Winter ziehen sie unter anderem nach Kalifornien und bewohnen bevorzugt Eukalyptuswälder.
Die Kieferntangare (Piranga ludoviciana) ist ein kleiner Vogel aus der Familie der Kardinäle (Cardinalidae). Entdeckt wurde der Vogel von Meriwether Lewis und William Clark während der Lewis-und-Clark-Expedition im Westen von Louisiana. Deshalb bekam er am Anfang von Alexander Wilson auch den Namen „Louisianatangare“.
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.
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 Jean Pierre Vieillot in 1808.[6][7] The species is monotypic; no subspecies are recognized.[7]
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.
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]
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]
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]
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]
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]
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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.
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]
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]
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]
This article incorporates public domain material from Piranga ludoviciana. United States Department of Agriculture.
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.
La tangara aliblanca migratoria (Piranga ludoviciana) es una especie de ave paseriforme de la familia Cardinalidae (aunque algunas fuentes sitúan su género, Piranga en Thraupidae). Anida en el oeste de Norteamérica e invierna en el sur de México y América Central.
Cuando llegan a la edad adulta, miden entre 15 y 19 cm de longitud. El macho es de cabeza roja, tornándose amarillento en la parte posterior de la misma. La nuca, el pecho, el vientre y la rabadilla son amarillos. La espalda, la cola y las alas son negras, pero estas últimas presentan dos rayas blancas con amarillo. El pico es amarillento muy claro y las patas negras.
La hembra, al igual que otras especies cercanas (en particular P. rubra y P. olivacea) tiene las partes dorsales verde oliva y las ventrales amarillas, además de tener el pico claro y las patas negras, pero se distingue porque, al igual que el macho, tiene dos rayas amarillas con blanco en las alas, que además presentan algo de negro. Adicionalmente hay un esbozo de raya supraocular amarillenta.
Es el tráupido que anida más al norte, desde el sur de Alaska hasta el extremo noroeste de México, principalmente en bosques de coníferas y bosques mixtos. Construyen un nido poco compacto sobre una rama horizontal de un árbol, generalmente una conífera. La hembra pone cuatro huevos verdes azulosos con manchas marrones.
En invierno migran hacia el sur, y en esta estación se distribuyen desde el sur de la península de Baja California y el centro-occidente de México hasta Costa Rica, en tierras bajas, alcanzando números poblacionales altos.
Se alimentan de insectos y frutos. Suelen alimentarse en lo alto de los árboles, o bien capturan insectos en el vuelo.
La tangara aliblanca migratoria (Piranga ludoviciana) es una especie de ave paseriforme de la familia Cardinalidae (aunque algunas fuentes sitúan su género, Piranga en Thraupidae). Anida en el oeste de Norteamérica e invierna en el sur de México y América Central.
Cuando llegan a la edad adulta, miden entre 15 y 19 cm de longitud. El macho es de cabeza roja, tornándose amarillento en la parte posterior de la misma. La nuca, el pecho, el vientre y la rabadilla son amarillos. La espalda, la cola y las alas son negras, pero estas últimas presentan dos rayas blancas con amarillo. El pico es amarillento muy claro y las patas negras.
La hembra, al igual que otras especies cercanas (en particular P. rubra y P. olivacea) tiene las partes dorsales verde oliva y las ventrales amarillas, además de tener el pico claro y las patas negras, pero se distingue porque, al igual que el macho, tiene dos rayas amarillas con blanco en las alas, que además presentan algo de negro. Adicionalmente hay un esbozo de raya supraocular amarillenta.
Es el tráupido que anida más al norte, desde el sur de Alaska hasta el extremo noroeste de México, principalmente en bosques de coníferas y bosques mixtos. Construyen un nido poco compacto sobre una rama horizontal de un árbol, generalmente una conífera. La hembra pone cuatro huevos verdes azulosos con manchas marrones.
En invierno migran hacia el sur, y en esta estación se distribuyen desde el sur de la península de Baja California y el centro-occidente de México hasta Costa Rica, en tierras bajas, alcanzando números poblacionales altos.
Se alimentan de insectos y frutos. Suelen alimentarse en lo alto de los árboles, o bien capturan insectos en el vuelo.
Piranga ludoviciana Piranga generoko animalia da. Hegaztien barruko Cardinalidae familian sailkatua dago.
Piranga ludoviciana Piranga generoko animalia da. Hegaztien barruko Cardinalidae familian sailkatua dago.
Piranga ludoviciana
Le Piranga à tête rouge (Piranga ludoviciana), aussi appelé Tangara joueur, est une espèce de passereaux de la famille des Cardinalidae, auparavant classée dans la famille des Thraupidae.
Cet oiseau mesure de 15 à 19 cm.
Le mâle a la tête rouge orangé, le corps d'un jaune franc avec le dos, les ailes et la queue noirs. Il présente deux barres alaires : la plus haute, plus courte et plus épaisse, est du même jaune que le reste du corps ; la plus basse, plus longue et plus fine, est blanc jaunâtre.
La femelle a le dessus gris tirant par endroits sur le vert et/ou le jaune, et le dessous d'un jaune léger. Elle possède elle aussi deux barres alaires ; mais la plus haute est d'un jaune moins vif que chez le mâle.
À la fin du printemps et au début de l'été, son régime alimentaire comprend surtout des insectes, capturés en vol au niveau de la haute canopée. Plus tard dans la saison, ils consomment beaucoup de baies et autres petits fruits[1].
Le chant du piranga à tête rouge ressemble un peu à celui du Merle d'Amérique : de courtes stances flutées, assez fortes, entrecoupées de courtes pauses, mais le chant du merle est plus harmonieux que celui du piranga[1]. Les cris d'appel du piranga à tête rouge en vol ressemble à de brefs "tchouwi"[2].
Il vit dans des forêts peu denses de conifères. Son aire de répartition couvre une partie de l'ouest du continent nord-américain. La limite nord de son aire de répartition va du sud de l'Alaska (Alaska Panhandle, aux États-Unis), à l'ouest, jusqu'au sud des Territoires du Nord-Ouest (au Canada), à l'est. La limite sud, en saison de nidification, se situe au nord du Mexique, mais cette espèce migratrice hiverne dans le Sud des États-Unis et au Mexique, jusqu'en Amérique centrale[1].
On compte deux sous-espèces :
Femelle
Mâle
Piranga à tête rouge aperçu à New York, c'est-à-dire en dehors de aire de répartition habituelle. Décembre 2020
Piranga ludoviciana
Le Piranga à tête rouge (Piranga ludoviciana), aussi appelé Tangara joueur, est une espèce de passereaux de la famille des Cardinalidae, auparavant classée dans la famille des Thraupidae.
De louisianatangare (Piranga ludoviciana) is een zangvogel uit de familie Cardinalidae (kardinaalachtigen).
Deze soort komt voor in westelijk Noord-Amerika en overwintert in westelijk Panama.
De louisianatangare (Piranga ludoviciana) is een zangvogel uit de familie Cardinalidae (kardinaalachtigen).
Västlig tangara[2] (Piranga ludoviciana) är en fågel i familjen kardinaler inom ordningen tättingar.[3] Den häckar västra Nordamerika och övervintrar söderut till västra Panama.[3] IUCN kategoriserar arten som livskraftig.[1]
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Wikimedia Commons har media som rör västlig tangara.
Wikispecies har information om Piranga ludoviciana.
Västlig tangara (Piranga ludoviciana) är en fågel i familjen kardinaler inom ordningen tättingar. Den häckar västra Nordamerika och övervintrar söderut till västra Panama. IUCN kategoriserar arten som livskraftig.
Piranga ludoviciana là một loài chim trong họ Cardinalidae.[1]
Piranga ludoviciana là một loài chim trong họ Cardinalidae.
Красноголовая пиранга[1], или западная танагра[2] (лат. Piranga ludoviciana) — вид певчих птиц из отряда воробьинообразных, распространённый в западной части Северной Америки.
Проявляют половой диморфизм. Самцы в период размножения выделяются ярко-красной окраской головы. Затылок, плечи и гузка жёлтые, спинка, крылья и хвост — чёрные, за исключением жёлтой полоски на крыльях. В остальное время они носят более скромное оливковое оперение с лёгким рыжим окрасом головы.
Красноголовая пиранга, или западная танагра (лат. Piranga ludoviciana) — вид певчих птиц из отряда воробьинообразных, распространённый в западной части Северной Америки.
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保全状況評価 LEAST CONCERN
分類 界 : 動物界 Animalia 門 : 脊索動物門 Chordata 亜門 : 脊椎動物亜門 Vertebrata 綱 : 鳥綱 Aves 目 : スズメ目 Passeriformes 科 : フウキンチョウ科 Thraupidae 属 : Piranga 種 : ニシフウキンチョウニシフウキンチョウ（学名：Piranga ludoviciana） は、鳥類の一種。
スズメ目> スズメ亜目> スズメ小目> スズメ上科> アトリ科> ホオジロ亜科> フウキンチョウ族
この項目は、鳥類に関連した書きかけの項目です。この項目を加筆・訂正などしてくださる協力者を求めています（ポータル鳥類 - PJ鳥類）。 
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