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Red crossbill

Loxia curvirostra

SUBFAMILY

Carduelinae

TAXONOMY

Loxia curvirostra Linnaeus, 1758. Six subspecies are recognized.

OTHER COMMON NAMES

English: Common crossbill; French: Bec-croisé des sapins; German: Fichtenkreuzschnabel; Spanish: Piquituerto Común.

PHYSICAL CHARACTERISTICS

The red crossbill has a body length of about 5.5 in (14 cm) and weighs about 1.4 oz (40 g). It has a rather heavy body, a short forked tail, and a stout beak in which the tips of the upper and lower mandibles cross over as an adaptation to extracting seeds from conifer cones. Males are colored overall brick-red, with blackish wings and tail. Females are a dull yellow-brown with darker wings. Juveniles have weakly crossed mandibles, grayolive upperparts and whitish underparts both streaked with dark brown, and a buff-yellow rump.

DISTRIBUTION

The red crossbill is an extremely widespread species that inhabits the boreal and montane forest regions of both North America and Eurasia. It occurs from coast to coast in suitable habitats on both continents. It periodically irrupts from its usual wintering regions and may then be abundant in areas where it is not usually seen.

HABITAT

Red crossbills breed and winter in pine-containing conifer forests of various kinds.

BEHAVIOR

Red crossbills are highly social birds, especially during the non-breeding season when they may occur in large flocks. The territorial song is a repeated series of simple chirps, often given in flight. The male displays to the female by flying above her, vibrating his wings, and delivering an in-flight song.

FEEDING ECOLOGY AND DIET

Red crossbills feed on the seeds of conifers, particularly species of pines. They use their peculiar, crossed bill to force the scales of conifer cones apart and then scoop the seed into their mouths with their tongues. Their diet also includes insects and caterpillars.

REPRODUCTIVE BIOLOGY

Breeding pairs are monogamous and solitary. The female builds a cup-shaped nest of twigs, bark, grass, and rootlets, lined with finer grasses, feathers, fur, hair, and moss. The nest is located on a tree branch far out from the trunk about 6.6–40 ft (2–12 m) above the ground. A clutch of three to four light green or blue eggs spotted with brown and lilac is incubated by the female for 12–18 days. The altricial young are brooded by the female and fed by both parents. They fledge in 15–20 days. Nestlings have straight mandibles that cross gradually after they have been out of the nest for about three weeks. One to two broods per year.

CONSERVATION STATUS

Not threatened. The red crossbill is a widespread and abundant species. Some populations, however, have declined greatly and are considered to be at risk. The subspecies native to the island of Newfoundland, for example, has become extremely rare. Logging operations have destroyed and continue to damage red crossbill habitat.

SIGNIFICANCE TO HUMANS

None known.

 
 
Western Bird Guide: red crossbill


Loxia curvirostra 5½-6½″ (14-16 cm). Near the size of a House Sparrow, with a heavy head and short tail. Note the crossed mandibles. The sound when it cracks the cones of evergreens often betrays its presence. It acts like a small parrot as it dangles while feeding. Male: Dull red, brighter on the rump; wings and tail blackish. Young males are more orange. Female: Dull olive-gray; yellowish on the rump and underparts. Juvenile: Striped above and below, suggesting a large Pine Siskin; note the bill.

Voice: Note, a hard jip-jip or jip-jip-jip. Song, finch-like warbled passages, jip-jip-jip-jeeaa-jeeaa; trills, chips.

Range: Conifer forests of N. Hemisphere. In N. America, south in mountains to Nicaragua; in East, locally to s. Appalachians. Erratic wanderings in winter.

Habitat: Conifers.


 
Wikipedia: Common Crossbill
Common Crossbill
Male Common Crossbill
Male Common Crossbill
Female Common Crossbill
Female Common Crossbill
Conservation status
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Class: Aves
Order: Passeriformes
Family: Fringillidae
Genus: Loxia
Species: L. curvirostra
Binomial name
Loxia curvirostra
Linnaeus, 1758

The Common Crossbill (Loxia curvirostra) is a small passerine bird in the finch family Fringillidae. It breeds in the spruce forests of North America, where it is known as Red Crossbill, as well as Europe and Asia; some populations (different species?) breed in pine forests in certain areas of all three continents, and in North America, also in Douglas-fir. It nests in conifers, laying 3–5 eggs.

This crossbill is mainly resident, but will regularly erupt south if its food source fails. This species will form flocks outside the breeding season, often mixed with other crossbills.

The crossbills are characterised by the mandibles crossing at their tips, which gives the group its English name. They are specialist feeders on conifer cones, particularly the various spruce species but also some populations (different species?) in Douglas-fir and various pine species, and the unusual bill shape is an adaptation to assist the extraction of the seeds from the cone.

Adult males tend to be red or orange in colour, and females green or yellow, but there is much variation.

This species is difficult to separate from Parrot Crossbill and Scottish Crossbill, both of which breed within its Eurasian range. The identification problem is less severe in North America, where only Red Crossbill and White-winged Crossbill occur.

Plumage distinctions from Parrot and Scottish Crossbills are negligible. The head and bill are smaller than in either of the other species. Care is needed to identify this species. The glip or chup call is probably the best indicator.

Work on vocalisation in North America suggest that, in that continent alone, there are eight or nine populations of Red Crossbill with different calls, which rarely if ever interbreed. These forms also vary in terms of bill size and structure, and specialise on the seed cones of different species of conifer. Few ornithologists seem inclined to give these forms species status at present.

Some large-billed, pine-feeding populations currently assigned to this species in the Mediterranean area may possibly be better referred to either Parrot Crossbill or alternatively to new species in their own right, but as yet, research into them is still at a very early stage. These include Balearic Crossbill L. curvirostra balearica and North African Crossbill L. curvirostra poliogyna, feeding primarily on Aleppo Pine (Pinus halepensis); Cyprus Crossbill L. curvirostra guillemardi, feeding primarily on European black pine (Pinus nigra); and an as-yet unidentified crossbill with a Parrot Crossbill-size bill feeding primarily on Bosnian Pine (Pinus heldreichii) in the Balkans. These populations also differ on plumage, with the Balearic, North African and Cyprus races having yellower males, and the Balkan type having deep purple-pink males; this however merely reflects the differing anthocyanin content of the cones they feed on, as these pigments are transferred to the feathers.

Crossbill Diversity

Distinct Eurasian Common Crossbill populations:

  • Balearic Crossbill, Loxia curvirostra balearica
  • North African Crossbill, Loxia c. poliogyna
  • Corsican Crossbill, Loxia c. corsicana
  • Cyprus Crossbill, Loxia c. guillemardi
  • Crimean Crossbill, Loxia c. mariae
  • Luzon Crossbill, Loxia c. luzoniensis
  • Annam Crossbill, Loxia c. meridionalis

As with Parrot and Scottish Crossbills all of the above are fairly sedentary forms associated with hard-coned Pinus species. The following are more associated with the softer cones of spruce and larch:

  • Altai Crossbill, Loxia c. altaiensis
  • Tien Shan Crossbill, Loxia c. tianschanica
  • Himalayan Crossbill, Loxia c. himalayensis
  • Japanese Crossbill, Loxia c. japonica


North American Red Crossbill subspecies list based on biometrics:

  • Newfoundland Crossbill, Loxia c. percna Possibly extinct
  • Lesser Crossbill, Loxia c. minor
  • Sitka Crossbill, Loxia c. sitkensis
  • Loxia c. neogaea
  • Rocky Mountain Crossbill, Loxia c. benti
  • Sierra Crossbill, Loxia c. grinnelli
  • Bendire Crossbill, Loxia c. bendirei
  • Mexican Crossbill, Loxia c. stricklandi
  • Central American Crossbill, Loxia c. mesamericana
  • South Hills Crossbill, Loxia c. ?


Jeff Groth's classification of North American Red Crossbill forms based on call-types:

  • Type 1, corresponds with Loxia c. neogaea
    • Recorded on Tsuga species, Picea glauca, Pinus strobus
  • Type 2, corresponds with Loxia c. benti/grinnelli/bendirei
    • Recorded on Pinus ponderosa scopulorum in the west and in various Pinus species in the east
  • Type 3, corresponds with Loxia c. sitkensis and Loxia c. minor
  • Type 4, corresponds with Loxia c. neogaea
  • Type 5, corresponds with Loxia c. benti/grinnelli/bendirei
  • Type 6, corresponds with Loxia c. stricklandi
    • Uses Pine species in Section Trifoliae
  • Type 7, corresponds with Loxia c. benti/grinnelli/bendirei
    • In terms of diet this type is possibly a generalist
  • Type 8, corresponds with Loxia c. percna
  • Type 9, corresponds with South Hills Crossbill


Summers' list of European Common Crossbill forms (with Parrot & Scottish) based on Flight/Excitement calls:

  • 1A, corresponds with "British" Crossbill
  • 2B, corresponds with "Wandering" Crossbill
  • 2D, corresponds with Parrot Crossbill Loxia pytyopsittacus
  • 3C, corresponds with Scottish Crossbill Loxia scotica
  • 3D, corresponds with Balearic Crossbill
  • 3E, corresponds with North African Crossbill
  • 4E, corresponds with "Glip" Crossbill
  • 5D, corresponds with Cyprus Crossbill


"The Sound Approach's" classification of European Common Crossbill types based on call-types:

  • "Wandering" Crossbill (Type A - flight call "Keep")
  • "Bohemian" Crossbill (Type B - flight call "Weet")
  • "Glip" Crossbill (Type C - flight call "Glip")
  • "Phantom" Crossbill (Type D - flight call "Jip")
  • "British" Crossbill (Type E - flight call "Chip")
  • "Scarce" Crossbill (Type F - flight call "Trip")
  • "Parakeet" Crossbill (Type X - flight call "Cheep")

References

External links

Wikimedia Commons has media related to:

Further reading

Book

Adkisson, C. S. 1996. Red Crossbill (Loxia curvirostra). In The Birds of North America, No. 256 (A. Poole and F. Gill, eds.). The Academy of Natural Sciences, Philadelphia, PA, and The American Ornithologists’ Union, Washington, D.C.

Thesis

  • Benkman CW. Ph.D. (1985). THE FORAGING ECOLOGY OF CROSSBILLS IN EASTERN NORTH AMERICA (AVES, BREEDING BEHAVIOR, MORPHOLOGY, CONIFERS). State University of New York at Albany, United States -- New York.
  • Coombs-Hahn TP. Ph.D. (1993). Integration of environmental cues to time reproduction in an opportunistic breeder, the red crossbill (Loxia curvirostra). University of Washington, United States -- Washington.
  • Groth JG. Ph.D. (1990). Cryptic species of nomadic birds in the red crossbill (Loxia curvirostra) complex of North America. University of California, Berkeley, United States -- California.
  • Simard JH. M.Sc. (2001). Habitat selection, ecological energetics, and the effects of changes in white pine forests on breeding red crossbills (Loxia curvirostra ) in Algonquin Provincial Park, Ontario. McGill University (Canada), Canada.
  • Smith JW. Ph.D. (2005). The role of coevolution in promoting ecological speciation in red crossbills (Loxia curvirostra complex). New Mexico State University, United States -- New Mexico.
  • Wren LS. M.Sc. (2001). Continental and regional distribution and abundance patterns of boreal cardueline finches: Influences of conifer seed availability. Memorial University of Newfoundland (Canada), Canada.

Articles

  • Alonso D, Arizaga J, Miranda R & Campos F. (2003). Comparative biometrics of common crossbills (Loxia curvirostra) on the Iberian Peninsula and the Bealearic Islands. Vogelwarte. vol 42, no 1-2. p. 116-117.
  • Alonso D, Arizaga J, Miranda R & Hernandez MA. (2006). Morphological diversification of common crossbill Loxia curvirostra populations within Iberia and the Balearics. Ardea. vol 94, no 1. p. 99-107.
  • Arnaiz-Villena A, Guillen J, Ruiz-de-Valle V, Lowy E, Zamora J, Varela P, Stefani D & Allende LM. (2001). Phylogeography of crossbills, bullfinches, grosbeaks, and rosefinches. Cellular and Molecular Life Sciences. vol 58, no 8. p. 1159-1166.
  • Barboza PS & Jorde DG. (2002). Intermittent fasting during winter and spring affects body composition and reproduction of a migratory duck. Journal of Comparative Physiology B-Biochemical Systemic and Environmental Physiology. vol 172, no 5. p. 419-434.
  • Benkman CW. (1987). Food Profitability and the Foraging Ecology of Crossbills. Ecological Monographs. vol 57, no 3. p. 251-267.
  • Benkman CW. (1988). Flock Size Food Dispersion and the Feeding Behavior of Crossbills. Behavioral Ecology & Sociobiology. vol 23, no 3. p. 167-176.
  • Benkman CW. (1988). On the Advantages of Crossed Mandibles an Experimental Approach. Ibis. vol 130, no 2. p. 288-293.
  • Benkman CW. (1993). ADAPTATION TO SINGLE RESOURCES AND THE EVOLUTION OF CROSSBILL (LOXIA) DIVERSITY. Ecological Monographs. vol 63, no 3. p. 305-325.
  • Benkman CW. (1993). The evolution, ecology, and decline of the red crossbill of Newfoundland. American Birds. vol 47, no 2. p. 225-229.
  • Benkman CW. (1999). The selection mosaic and diversifying coevolution between crossbills and lodgepole pine. American Naturalist. vol 153, p. S75-S91.
  • Benkman CW. (2003). Divergent selection drives the adaptive radiation of crossbills. Evolution. vol 57, no 5. p. 1176-1181.
  • Benkman CW, Colquitt JS, Gould WR, Fetz T, Keenan PC & Santisteban L. (2005). Can selection by an ectoparasite drive a population of red crossbills from its adaptive peak?. Evolution. vol 59, no 9. p. 2025-2032.
  • Benkman CW, Holimon WC & Smith JW. (2001). The influence of a competitor on the geographic mosaic of coevolution between crossbills and lodgepole pine. Evolution. vol 55, no 2. p. 282-294.
  • Benkman CW & Lindholm AK. (1991). THE ADVANTAGES AND EVOLUTION OF A MORPHOLOGICAL NOVELTY. Nature. vol 349, no 6309. p. 519-520.
  • Benkman CW & Miller RE. (1996). Morphological evolution in response to fluctuating selection. Evolution. vol 50, no 6. p. 2499-2504.
  • Benkman CW, Parchman TL, Favis A & Siepielski AM. (2003). Reciprocal selection causes a coevolutionary arms race between crossbills and lodgepole pine. American Naturalist. vol 162, no 2. p. 182-194.
  • Brauning DW, Brittingham MC, Gross DA, Leberman RC, Master TL & Mulvihill RS. (1994). Pennsylvania breeding birds of special concern: A listing rational and status update. Journal of the Pennsylvania Academy of Science. vol 68, no 1. p. 3-28.
  • Brazier FH. (1996). A second breeding record of Red Crossbill in Regina. Blue Jay. vol 54, no 1.
  • Clark WH. (1981). Highway Mortality of the Red Crossbill Loxia-Curvirostra. Journal of the Idaho Academy of Science. vol 17, no 1. p. 1-2.
  • Clouet M. (2000). The breeding biology of the Common Crossbill Loxia Curvirostra in the Central Pyrenees. Bird Study. vol 47, p. 186-194.
  • Clouet M. (2003). Bill size and breeding periode of pine forest crossbills. Revue D Ecologie-La Terre Et La Vie. vol 58, no 4. p. 419-433.
  • Clouet M & Goar J-L. (2001). Note on the Philippine cross-bill Loxia curvirostra luzoniensis. Alauda. vol 69, no 2. p. 331-334.
  • Coffey K, Benkman CW & Milligan BG. (1999). The adaptive significance of spines on pine cones. Ecology. vol 80, no 4. p. 1221-1229.
  • Constantine M, & "The Sound Approach". (2006). The Sound Approach to Birding. A guide to understanding bird sound. ISBN-10: 9081093312
  • Cornelius JM, Breuner CW & Hahn TP. (2004). Effects of food reduction on stress reactivity in an irruptive nomad, the red crossbill. Integrative and Comparative Biology. vol 44, no 6. p. 684-684.
  • Dinsmore JJ. (1998). Iowa's avifauna: Recent changes and prospects for the future. Journal of the Iowa Academy of Science. vol 105, no 3. p. 115-122.
  • Edelaar P. (2003). Are there morphological differences between the vocal types of the common crossbill?. Vogelwarte. vol 42, no 1-2. p. 115-116.
  • Edelaar P. (2003). Is there assortative mating between the vocal types of the common crossbill?. Vogelwarte. vol 42, no 1-2.
  • Edelaar P & Benkman CW. (2006). Replicated population divergence caused by localized coevolution? A test of three hypotheses in the red crossbill-lodgepole pine system. Journal of Evolutionary Biology. vol 19, no 5. p. 1651-1659.
  • Edelaar P, Phillips RE & Knops P. (2005). Sexually dimorphic body plumage in juvenile Crossbills. Wilson Bulletin. vol 117, no 4. p. 390-393.
  • Edelaar P & Terpstra K. (2004). The nominate subspecies of the Common Crossbill Loxia c. curvirostra polytypic? I. Morphological differences among years at a single site. Ardea. vol 92, no 1. p. 93-102.
  • Förschler MI, Förschler L & Dorka U. (2006). Population fluctuations of siskins Carduelis spinus, common crossbills Loxia curvirostra, and citril finches Carduelis citrinella in relationship to flowering intensity of spruce Picea abies. Ornis Fennica. vol 83, no 2. p. 91-96. http://www.birdlife.fi/julkaisut/of/pdf/vol83-2/6F%F6rschler2524.pdf
  • Frost MP. (1985). Citril Finches Serinus-Citrinella and Crossbills Loxia-Curvirostra Eating Minerals. British Birds. vol 78, no 1.
  • Genard M & Lescourret F. (1987). The Common Crossbill Loxia-Curvirostra in the Pyrenees France Some Observations on Its Habitats and on Its Relations with Conifer Seeds. Bird Study. vol 34, no 1. p. 52-63.
  • Gilbert FF & Allwine R. (1991). Spring Bird Communities in the Oregon Cascade Range USA. U S Forest Service General Technical Report PNW. vol 285, p. 145-159.
  • Groth JG. (1988). Resolution of Cryptic Species in Appalachian Red Crossbills. Condor. vol 90, no 4. p. 745-760.
  • Groth JG. (1993). Call matching and positive assortative mating in Red Crossbills. The Auk. vol 110, no 2. p. 398.
  • Hahn T. (1990). PHYSIOLOGICAL CORRELATES OF OPPORTUNISTIC BREEDING IN THE RED CROSSBILL. American Zoologist. vol 30, no 4. p. A53-A53.
  • Hahn T. (1992). Seasonal components of reproductive function in a reproductive opportunist, the red crossbill, Loxia curvirostra. American Zoologist. vol 32, no 5.
  • Hahn TP. (1994). Crossbill diversity -- Evolutionary Differentiation in Morphology, Vocalizations, and Allozymes Among Nomadic Sibling Species in the North American Red Crossbill (Loxia curvirostra) Complex by J. G. Groth. The Condor. vol 96, no 3. p. 835.
  • Hahn TP. (1995). Integration of Photoperiodic and Food Cues to Time Changes in Reproductive Physiology by an Opportunistic Breeder, the Red Crossbill, Loxia curvirostra (Aves: Carduelinae). Journal of Experimental Zoology. vol 272, no 3. p. 213-226.
  • Hahn TP. (1996). Habitat preferences and biogeography of cryptic species in the North American red crossbill complex (Loxia curvirostra; Aves: Carduelinae). American Zoologist. vol 36, no 5.
  • Hahn TP. (1998). Reproductive seasonality in an opportunistic breeder, the red crossbill, Loxia curvirostra. Ecology. vol 79, no 7. p. 2365-2375.
  • Hau M. (2001). Timing of breeding in variable environments: Tropical birds as model systems. Hormones and Behavior. vol 40, no 2. p. 281-290.
  • Hau M, Wikelski M & Wingfield JC. (2000). Visual and nutritional food cues fine-tune timing of reproduction in a neotropical rainforest bird. Journal of Experimental Zoology. vol 286, no 5. p. 494-504.
  • Herbers JR, Serrouya R & Maxcy KA. (2004). Effects of elevation and forest cover on winter birds in mature forest ecosystems of southern British Columbia. Canadian Journal of Zoology-Revue Canadienne De Zoologie. vol 82, no 11. p. 1720-1730.
  • Hernandez M, Alonso D, Arizaga J, Amezcoa A, Alda F, Murua A, Schroder P-C & Campos F. (2003). Comparative molecular study of populations of common crossbill (Loxia curvirostra) on the Iberian Peninsula and the Balearic Islands. Vogelwarte. vol 42, no 1-2.
  • Hill GE & Benkman CW. (1995). Exceptional response by female red crossbills to dietary carotenoid supplementation. The Wilson Bulletin. vol 107, no 3. p. 555.
  • Hogstad O. (1990). Winter Territoriality and the Advantages of Social Foraging in the Treecreeper Certhia-Familiaris. Fauna Norvegica Series C Cinclus. vol 13, no 2. p. 57-64.
  • Holimon WC, Benkman CW & Willson MF. (1998). The importance of mature conifers to red crossbills in southeast Alaska. Forest Ecology and Management. vol 102, no 2-3. p. 167-172.
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  • Jacobs JD & Wingfield JC. (2000). Endocrine control of life-cycle stages: A constraint on response to the environment?. Condor. vol 102, no 1. p. 35-51.
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  • Johnson NK, Marten JA & Ralph CJ. (1989). Genetic Evidence for the Origin and Relationships of Hawaiian Honeycreepers Aves Fringillidae. Condor. vol 91, no 2. p. 379-396.
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  • Knox AG. (1990). THE SYMPATRIC BREEDING OF COMMON AND SCOTTISH CROSSBILLS LOXIA-CURVIROSTRA AND LOXIA-SCOTICA AND THE EVOLUTION OF CROSSBILLS. Ibis. vol 132, no 3. p. 454-466.
  • Koenig WD. (2001). Synchrony and periodicity of eruptions by boreal birds. Condor. vol 103, no 4. p. 725-735.
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  • Parchman TL & Benkman CW. (2002). Diversifying coevolution between crossbills and black spruce on Newfoundland. Evolution. vol 56, no 8. p. 1663-1672.
  • Parchman TL, Benkman CW & Britch SC. (2006). Patterns of genetic variation in the adaptive radiation of New World crossbills (Aves : Loxia). Molecular Ecology. vol 15, no 7. p. 1873-1887.
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Animal Encyclopedia. Grzimek's Animal Life Encyclopedia. Copyright © 2005 by The Gale Group, Inc. All rights reserved.  Read more
Western Bird Guide. Peterson Field Guide to Western Birds, by Roger Tory Peterson. Copyright © 1990 by Houghton Mifflin Company. Published by Houghton Mifflin Company. All rights reserved.  Read more
Wikipedia. This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Common Crossbill" Read more

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