thumb|Immature male, Honduras

thumb|Pheucticus ludovicianus - Rose-breasted Grosbeak

The rose-breasted grosbeak (Pheucticus ludovicianus), colloquially called "cut-throat" due to its coloration, is a large, seed-eating grosbeak in the cardinal family (Cardinalidae). It is primarily a foliage gleaner. Males have black heads, wings, backs, and tails, and a bright rose colored patch on their white breast. Males and females exhibit marked sexual dimorphism.

Breeding habitat consists of cool-temperate open deciduous woods throughout much of eastern North America, with migration to tropical America in winter. Rose-breasted grosbeaks have an average maximum lifespan of 7.3 years in the wild, and up to 24 years in captivity. Death in the wild is generally due to collision with objects (buildings, cars, etc.) and predation, to eggs, nestlings and adults.

Taxonomy

In 1760 the French zoologist Mathurin Jacques Brisson included a description of the rose-breasted grosbeak in his Ornithologie based on a specimen collected in Louisiana. He used the French name Le gros-bec de la Louisiane and the Latin Coccothraustes Ludoviciana. Although Brisson coined Latin names, these do not conform to the binomial system and are not recognised by the International Commission on Zoological Nomenclature. When in 1766 the Swedish naturalist Carl Linnaeus updated his Systema Naturae for the twelfth edition, he added 240 species that had been previously described by Brisson. This species is now placed in the genus Pheucticus that was introduced by the German naturalist Ludwig Reichenbach in 1850. The species is monotypic.

Description

thumb|right|Immature male

thumb|right|Two males at feeder

Adult birds are long, span across the wings and weigh . Grosbeaks measured during migration in the West Indies averaged , while those banded in Pennsylvania average about . Very little sexual dimorphism in size is seen; females were found to be marginally smaller in standard measurements, but in some seasons were marginally heavier than males when banded in Pennsylvania. At all ages and in both sexes, the beak is dusky horn-colored, and the feet and eyes are dark.

The adult male in breeding plumage has a black head, wings, back, and tail, and a bright rose-red patch on its breast; the wings have two white patches and rose-red linings. Its underside and rump are white. Males in nonbreeding plumage have largely white underparts, supercilium, and cheeks. The upperside feathers have brown fringes, and most wing feathers white ones, giving a scaly appearance. The bases of the primary remiges are also white. The coloration renders the adult male rose-breasted grosbeak (even while wintering) unmistakable if seen well.

The adult female has dark grey-brown upperparts – darker on wings and tail – a white supercilium, a buff stripe along the top of the head, and black-streaked white underparts, which except in the center of the belly have a buff tinge. The wing linings are yellowish, and on the upperwing are two white patches like in the summer male. Immatures are similar, but with pink wing-linings and less prominent streaks and usually a pinkish-buff hue on the throat and breast. At one year of age—in their first breeding season—males are scaly above like fully adult males in winter plumage, and still retain the immature's browner wings. Unlike males, females can easily be confused with the black-headed grosbeak (Pheucticus melanocephalus) where their ranges overlap in the central United States and south-central Canada. The rose-breasted grosbeak female has slightly darker brown markings on the underside, paler rather yellowish streaking on both the head and wings and paler, pinkish (rather than bi-colored) bill when compared to the female black-headed grosbeak. A potential confusion species also is the female purple finch (Haemorhous purpureus), but that species is noticeably smaller with a less robust bill and a notched tail.

The song is a subdued mellow warbling, resembling a more refined, sweeter version of the American robin's (Turdus migratorius). Males start singing early, occasionally even when still in winter quarters. The call is a sharp pink or pick, somewhat reminiscent of a woodpecker call.

Distribution and habitat

The rose-breasted grosbeak's breeding habitat is open deciduous woods across most of Canada and the northeastern United States. In particular, the northern birds migrate south through the United States east of the Rocky Mountains, to winter from central-southern Mexico through Central America and the Caribbean to Peru and Venezuela. The southern limit of its wintering range is not well known; it was, for example, only recorded in the Serranía de las Quinchas (Colombia) in the 1990s. In winter, they prefer more open woodland, or similar habitat with a loose growth of trees, such as forest edges, parks, gardens, and plantations, ranging from sea level into the hills, e.g. up to above mean sea level in Costa Rica. Since 1966 the rose-breasted grosbeak has experienced a greater than 1.5% yearly decline in population throughout the eastern part of its summer range, but a coincident >1.5% yearly increase in western parts of its summer range.

Migration

The first birds leave the breeding grounds as early as August, while the last ones do not return until mid-late May. In general, however, they migrate south in late September or in October, and return in late April or early May. It appears as if they remain on their breeding grounds longer today than they did in the early 20th century, when migrants were more commonly seen in May and August than in April or September. The rose-breasted grosbeak occurs as a very rare vagrant in western Europe. During breeding it is fairly territorial; in winter, it typically travels in small groups, and sometimes in larger flocks of a dozen or more.

Behaviour and ecology

Breeding

Rose-breasted grosbeaks were the only one of 70 migratory songbird species in the eastern United States shown in males to have produced sperm while still far south of their breeding location. Male grosbeaks tend to arrive a few days to a week before the females and pair formation apparently occurs on the breeding grounds. Nest building begins from as early as early May in Tennessee to as late as early June further north in Saskatchewan. Egg laying may occur anytime from mid-May to mid-July, as has been recorded in Quebec. Usually only a single brood is laid by these grosbeaks each summer but second broods are suspected in Canada and confirmed in semi-captivity. Both the male and the female apparently participate in selecting and building the nest, which is on a tree branch, over vines or any elevated woody vegetation. Nests have been recorded at off the ground, averaging high, almost always in the vicinity of openings in woodlands. Nests are typical of many passerines in both construct, material and size, made from leaves, twigs, rootlets or hair. Clutches are from 1 to 5 eggs, normally being 3–4, being pale blue to green with purplish to brownish red spotting. Males do a third of the incubation roughly, the female doing the remaining amount, and incubation can last from 11 to 14 days. Captive grosbeaks have been recorded living up to 24 years of age, making them quite a long-living passerine excluding the pressures of surviving in the wild. Although frequently targeted by the brood parasite, the brown-headed cowbird (Molothrus ater), the rose-breasted grosbeak is apparently able to recognize cowbird eggs and has been seen to aggressively displace cowbirds near the nest. Typically, fewer than 7% of grosbeak nests have cowbird eggs per one study. Per the U.S. Bird Banding Laboratory, as of 1997, rose-breasted grosbeaks recovered when dead have largely collided with objects, including buildings and cars (17.2%) or had been shot (10%; mostly before 1960), 3.6% of the fatalities were caught by cats, 0.8% caught by dogs. Mortality due to natural causes, including disease, natural predators and inclement weather go largely unreported. It is known the main cause of nesting failure is predation. Natural predators of eggs and nestlings include blue jays (Cyanocitta cristata), common grackles (Quiscalus quiscula), raccoons (Procyon lotor), gray (Sciurus carolinensis) and red (Tamiasciurus hudsonicus) squirrels. Confirmed predators of adults include both Cooper's (Accipiter cooperii) and sharp-shinned hawks (Accipiter striatus) as well as northern harriers (Circus cyaenus), eastern screech-owls (Megascops asio) and short-eared owls (Asio flammeus).

Diet

The rose-breasted grosbeak forages in shrubs or trees for insects, seeds and berries, also catching insects in flight and occasionally eating nectar. It usually keeps to the treetops, and only rarely can be seen on the ground. In the winter quarters, they can be attracted into parks, gardens, and possibly even to bird feeders by fruit like Trophis racemosa. They also survive on blackberries, mulberries, seeds of smartweed, pigweed, raspberries, and milkweed, in addition to sunflower seeds, garden peas, oats, wheat, tree blossoms, tree buds, and developed natural product. Other notable winter food includes jacaranda seeds and the fruits of the introduced busy Lizzy (Impatiens walleriana). In grosbeaks from the north-central United States and southern Canada, 52% of the stomach contents were comprised by invertebrates, predominantly beetles; 19.3% was made up of wild fruits; 15.7% by weed seeds; 6.5% by cultivated fruits and plants, including peas, corn (Zea mays), oats (Avena sativa) and wheat (Triticum vulgare); and the remaining 6.5% by other plant material, including tree buds and flowers.

Status

Fires are necessary to maintain many kinds of grassland (see Fire ecology). Fire suppression in the late-20th century allowed forests to spread on the Great Plains into areas where recurring fires would otherwise have maintained grassland. This allowed hybridization with the black-headed grosbeak subspecies P. melanocephalus papago. Range expansions also seem to have occurred elsewhere, for example in northern Ohio, where it bred rarely if at all in the first decade of the 1900s, but it is by no means an uncommon breeder today. In general, though it requires mature woodland to breed and is occasionally caught as a cage bird, the rose-breasted grosbeak is not at all rare, and not considered a threatened species by the IUCN. <!-- Stiles & Skutch (1989), OOS (2004), BLI (2008)</ref> --> Its average maximum lifespan in the wild is 7.3 years.

References

  • Rose-breasted Grosbeak Species Account - Cornell Lab of Ornithology
  • Rose-breasted Grosbeak - Pheucticus ludovicianus - USGS Patuxent Bird Identification InfoCenter
  • Rose-breasted Grosbeak eNature.com
  • (for Barbuda, Cuba, El Salvador, Grenada, Grenadines of Grenada, United States) with RangeMap at bird-stamps.org

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Further reading

Books

  • Wyatt, V. E., and C. M. Francis. 2002. Rose-breasted Grosbeak (Pheucticus ludovicianus). In The Birds of North America, No. 692 (A. Poole and F. Gill, eds.). The Birds of North America, Inc., Philadelphia, PA.

Theses

  • Cook WE. Ph.D. (1989). A morphological comparison between geographically separated populations of selected species of North American migratory and nonmigratory birds (Aves:Cardinalinae, Troglodytidae). The Union Institute, United States – Ohio.
  • Dunham DW. Ph.D. (1964). BEHAVIOR OF THE ROSE-BREASTED GROSBEAK, PHEUCTICUS LUDOVICIANUS (LINNAEUS). Cornell University, United States – New York.
  • Langley PJW. M.Sc. (1976). The breeding behavior and reproductive strategy of the rose-breasted grosbeak Pheucticus ludovicianus L. The University of Western Ontario (Canada), Canada.
  • Smith LA. M.Sc. (2005). The impacts of silvicultural practices on the rose-breasted grosbeak (Pheucticus ludovicianus) in woodlots of southwestern Ontario, Canada. Trent University (Canada), Canada.

Articles

  • Anderson JF, Johnson RC, Magnarelli LA & Hyde FW. (1986). "Involvement of Birds in the Epidemiology of the Lyme Disease Agent Borrelia-Burgdorferi". Infection & Immunity. vol 51, no 2. p. 394–396.
  • Bosque C & Lentino M. (1987). "The Passage of North American Migratory Land Birds through Xerophytic Habitats on the Western Coast of Venezuela". Biotropica. vol 19, no 3. p. 267–273.
  • Burke DM & Nol E. (2000). "Landscape and fragment size effects on reproductive success of forest-breeding birds in Ontario". Ecological Applications. vol 10, no 6. p. 1749–1761.
  • Campbell E. (1975). "Rose-Breasted Grosbeak in Winter". Loon. vol 47, no 2.
  • Cannell PF, Cherry JD & Parkes KC. (1983). "Variation and Migration Overlap in Flight Feather Molt of the Rose-Breasted Grosbeak Pheucticus-Ludovicianus". Wilson Bulletin. vol 95, no 4. p. 621–627.
  • Caryl PG. (1979). "Communication by Agonistic Displays What Can Games Theory Contribute to Ethology". Behaviour. vol 68, no 1–2. p. 136–169.
  • Crawford P. (1971). "Winter Rose-Breasted Grosbeak at Gallatin". Migrant. vol 42, no 3. p. 61–62.
  • Cumming EE & Diamond AW. (2002). "Songbird community composition versus forest rotation age in Saskatchewan boreal mixedwood forest". Canadian Field Naturalist. vol 116, no 1. p. 69–75.
  • Doyle TJ. (2002). "A verifiable winter record of Rose-breasted Grosbeak in Florida". Florida Field Naturalist. vol 30, no 4. p. 135–137.
  • Doyon F, Gagnon D & Giroux JF. (2005). "Effects of strip and single-tree selection cutting on birds and their habitat in a Southwestern Quebec northern hardwood forest". Forest Ecology and Management. vol 209, no 1–2. p. 101–115.
  • Duguay JP, Wood PB & Nichols JV. (2001). "Songbird abundance and avian nest survival rates in forests fragmented by different silvicultural treatments". Conservation Biology. vol 15, no 5. p. 1405–1415.
  • Eastman J. (1970). "Grazing of a Rose-Breasted Grosbeak on a Green Burn". Jack Pine Warbler. vol 48, no 4. p. 111–112.
  • Farfan-Ale JA, Blitvich BJ, Lorono-Pino MA, Marlenee NL, Rosado-Paredes EP, Garcia-Rejon JE, Flores-Flores LF, Chulim-Perera L, Lopez-Uribe M, Perez-Mendoza G, Sanchez-Herrera I, Santamaria W, Moo-Huchim J, Gubler DJ, Cropp BC, Calisher CH & Beaty BJ. (2004). "Longitudinal studies of West Nile virus infection in avians, Yucatan State, Mexico". Vector-Borne and Zoonotic Diseases. vol 4, no 1. p. 3–14.
  • Fink LC. (1968). "Rose-Breasted Grosbeaks in Small Flock in Atlanta Georgia USA Pheucticus-Ludovicianus Behavior". Oriole. vol 33, no 3.
  • Fink LC. (1972). "Late Fall Record of Rose-Breasted Grosbeak in Atlanta". Oriole. vol 37, no 1.
  • Francis CM & Cooke F. (1990). "Differential Timing of Spring Migration in Rose-Breasted Grosbeaks". Journal of Field Ornithology. vol 61, no 4. p. 404–412.
  • Friesen L, Cadman MD & Mackay RJ. (1999). "Nesting success of Neotropical migrant songbirds in a highly fragmented landscape". Conservation Biology. vol 13, no 2. p. 338–346.
  • Friesen LE, Wyatt VE & Cadman MD. (1999). "Nest reuse by Wood Thrushes and Rose-breasted Grosbeaks". Wilson Bulletin. vol 111, no 1. p. 132–133.
  • Hobson KA & Schieck J. (1999). "Changes in bird communities in boreal mixedwood forest: Harvest and wildfire effects over 30 years". Ecological Applications. vol 9, no 3. p. 849–863.
  • Holmes RT. (1976). "Body Composition Lipid Reserves and Caloric Densities of Summer Birds in a Northern Deciduous Forest". American Midland Naturalist. vol 96, no 2. p. 281–290.
  • Holmes RT. (1986). "Foraging Patterns of Forest Birds Male-Female Differences". Wilson Bulletin. vol 98, no 2. p. 196–213.
  • Holmes RT & Robinson SK. (1981). Tree Species Preferences of Foraging Insectivorous Birds in a Northern Hardwoods Forest. Oecologia. vol 48, no 1. p. 31–35.
  • Holmes RT & Sherry TW. (1988). "Assessing Population Trends of New Hampshire USA Forest Birds Local Vs. Regional Patterns". Auk. vol 105, no 4. p. 756–768.
  • Hoving EJ & Sealy SG. (1987). "Species and Age Composition of a Sample of Birds Killed in Fall 1979 at a Manitoba Canada Tv Tower". Prairie Naturalist. vol 19, no 2. p. 129–134.
  • Janssen RB. (1973). "Late Rose-Breasted Grosbeak". Loon. vol 45, no 1.
  • Kirk DA, Diamond AW, Smith AR, Holland GE & Chytyk P. (1997). "Population changes in boreal forest birds in Saskatchewan and Manitoba". Wilson Bulletin. vol 109, no 1. p. 1–27.
  • Krager JM. (1969). Rose-Breasted Grosbeak in Madison. Passenger Pigeon. vol 31, no 4. p. 182–183.
  • Kroodsma RL. (1974). Species Recognition Behavior of Territorial Male Rose-Breasted Grosbeak and Black-Headed Grosbeak Pheucticus. Auk. vol 91, no 1. p. 54–64.
  • Lacki MJ. (2000). Surveys of bird communities on Little Black and Black mountains: Implications for long-term conservation of Montane birds in Kentucky. Journal of the Kentucky Academy of Sciences. vol 61, no 1. p. 50–59.
  • Latham R. (1971). The Rose-Breasted Grosbeak at Orient Long Island. Engelhardtia. vol 4, no 4.
  • Leberman RC. (1984). Rose Underwings in Female Rose-Breasted Grosbeaks Pheucticus-Ludovicianus. Journal of Field Ornithology. vol 55, no 4. p. 486–487.
  • Link WA & Hahn DC. (1996). Empirical Bayes estimation of proportions with application to cowbird parasitism rates. Ecology. vol 77, no 8. p. 2528–2537.
  • Merrill SB, Cuthbert FJ & Oehlert G. (1998). Residual patches and their contribution to forest-bird diversity on northern Minnesota aspen clearcuts. Conservation Biology. vol 12, no 1. p. 190–199.
  • Nol E, Francis CM & Burke DM. (2005). Using distance from putative source woodlots to predict occurrence of forest birds in putative sinks. Conservation Biology. vol 19, no 3. p. 836–844.
  • Parrish JD. (1997). Patterns of frugivory and energetic condition in Nearctic landbirds during autumn migration. Condor. vol 99, no 3. p. 681–697.
  • Pittaway R & Iron J. (2006). Erythristic Rose-breasted Grosbeak. Ontario Birds. vol 24, no 1. p. 2–5.
  • Ports MA. (1981). Miscellaneous Summer Records of Birds from Southwestern Kansas USA. Transactions of the Kansas Academy of Science. vol 84, no 2. p. 109–114.
  • Quay WB. (1985). Cloacal Sperm in Spring Migrants Occurrence and Interpretation. Condor. vol 87, no 2. p. 273–280.
  • Quay WB. (1989). Timing of Sperm Releases and Inseminations in Resident Emberizids a Comparative Study. Condor. vol 91, no 4. p. 941–961.
  • Ritchie TL. (1980). 2 Mid Pleistocene Avi Faunas from Coleman Florida USA. Bulletin of the Florida State Museum Biological Sciences. vol 26, no 1. p. 1–36.
  • Robinson SK & Holmes RT. (1982). Foraging Behavior of Forest Birds the Relationships among Search Tactics Diet and Habitat Structure. Ecology. vol 63, no 6. p. 1918–1931.
  • Rothstein SI. (1973). Extreme Overlap between 1st and 2nd Nestings in the Rose-Breasted Grosbeak. Wilson Bulletin. vol 85, no 2. p. 242–243.
  • Siljenberg AM. (1973). Songs and Sounds of Rose-Breasted Grosbeak. South Dakota Bird Notes. vol 26, no 2.
  • Skowron C & Kern M. (1980). The Insulation in Nests of Selected North American Song Birds. Auk. vol 97, no 4. p. 816–824.
  • Smith LA, Burke DM, Nol E & Elliott KA. (2006). The effects of partial cutting on the Rose-breasted Grosbeak: abundance, food availability, and nest survival. Canadian Journal of Forest Research. vol 36, no 5. p. 1087–1096.
  • Steffee ND. (1969). Rose-Breasted Grosbeak Pheucticus-Ludovicianus Record Kissimmee Florida USA. Florida Naturalist. vol 42, no 1.
  • Stutchbury BJM, Capuano B & Fraser GS. (2005). Avian frugivory on a gap-specialist, the red elderberry (Sambucus racemosa). Wilson Bulletin. vol 117, no 4. p. 336–340.
  • Voelker T. (1973). Recovery of a Banded Rose-Breasted Grosbeak. Loon. vol 45, no 1. p. 24–25.
  • Welsh CJE & Healy WM. (1993). Effect of even-aged timber management on bird species diversity and composition in northern hardwoods of New Hampshire. Wildlife Society Bulletin. vol 21, no 2. p. 143–154.
  • Wyatt VE. (1997). Use of Anemone canadensis in Rose-breasted Grosbeak nests. Ontario Birds. vol 15, no 2. p. 74–75.

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