|Scavenging on a beach in Dorset, England|
|Carrion crow range Year-Round Range Summer Range Winter Range|
Taxonomy and systematics
The carrion crow was one of the many species originally described by Linnaeus in his 18th-century work Systema Naturae, and it still bears its original name of Corvus corone. The binomial name is derived from the Latin Corvus, "Raven", and Greek korone/κορωνη, "crow".
The hooded crow, formerly regarded as a subspecies, has been split off as a separate species, and there is some discussion whether the eastern carrion crow (C. c. orientalis) is distinct enough to warrant specific status; the two taxa are well separated, and it has been proposed they could have evolved independently in the wetter, maritime regions at the opposite ends of the Eurasian landmass.
Along with the hooded crow, the carrion crow occupies a similar ecological niche in Eurasia to the American crow (C. brachyrhyncos) in North America.
The plumage of the carrion crow is black with a green or purple sheen, much greener than the gloss of the rook. The bill, legs and feet are also black. It can be distinguished from the common raven by its size (48–52 cm or 19 to 20 inches in length as compared to an average of 63 centimetres (25 inches) for ravens) and from the hooded crow by its black plumage. The carrion crow has a wingspan of 84–100 cm or 33 to 39 inches and weighs 400–600 grams.
There is frequent confusion between the carrion crow and the rook, another black corvid found within its range. The beak of the crow is stouter and in consequence looks shorter, and whereas in the adult rook the nostrils are bare, those of the crow are covered at all ages with bristle-like feathers. As well as this, the wings of a carrion crow are proportionally shorter and broader than those of the rook when seen in flight.
Distribution and genetic relationship to hooded crows
The carrion crow (Corvus corone) and hooded crow (Corvus cornix, including its slightly larger allied form or race C. c. orientalis) are two very closely related species whose geographic distributions across Europe are illustrated in the accompanying diagram. It is believed that this distribution might have resulted from the glaciation cycles during the Pleistocene, which caused the parent population to split into isolates which subsequently re-expanded their ranges when the climate warmed causing secondary contact.
Poelstra and coworkers sequenced almost the entire genomes of both species in populations at varying distances from the contact zone to find that the two species were genetically identical, both in their DNA and in its expression (in the form of mRNA), except for the lack of expression of a small portion (<0.28%) of the genome (situated on avian chromosome 18) in the hooded crow, which imparts the lighter plumage colouration on its torso. Thus the two species can viably hybridize, and occasionally do so at the contact zone, but the all-black carrion crows on the one side of the contact zone mate almost exclusively with other all-black carrion crows, while the same occurs among the hooded crows on the other side of the contact zone.
It is therefore clear that it is only the outward appearance of the two species that inhibits hybridization. The authors attribute this to assortative mating (rather than to ecological selection), the advantage of which is not clear, and it would lead to the rapid appearance of streams of new lineages, and possibly even species, through mutual attraction between mutants. Unnikrishnan and Akhila propose, instead, that koinophilia is a more parsimonious explanation for the resistance to hybridization across the contact zone, despite the absence of physiological, anatomical or genetic barriers to such hybridization. The carrion crow is also found in the mountains and forests of Japan and also in the cities of Japan.
Behaviour and ecology
The rook is generally gregarious and the crow solitary, but rooks occasionally nest in isolated trees, and crows may feed with rooks; moreover, crows are often sociable in winter roosts. The most distinctive feature is the voice. The rook has a high-pitched kaaa, but the crow's guttural, slightly vibrant, deeper croaked kraa is distinct from any note of the rook.
The carrion crow is noisy, perching on a vantage point such as a building or the top of a tree and calling three or four times in quick succession, with a slight pause between each series of croaks. During each series of calls, a crow may perform an accompanying gesture, bowing its head and neck downwards with each caw. The wing-beats are slower, more deliberate than those of the rook.
Carrion crows can become tame near humans, and can often be found near areas of human activity or habitation including cities, moors, woodland, sea cliffs and farmland where they compete with other social birds such as gulls and ducks for food in parks and gardens.
Like other species of corvid, carrion crows will actively harass predators and competitors that enter their territory or threaten them or their offspring, and will engage in group mobbing behaviour as a method to defend themselves.
Like all corvids, carrion crows show intelligent behaviour. For example, they can discriminate between numerosities up to 30, flexibily switch between rules, and recognise human and crow faces. Given the difference in brain architecture in crows compared to primates, these abilities suggest that their intelligence is realised as a product of convergent evolution.
Though an eater of carrion of all kinds, the carrion crow will eat insects, earthworms, grain, fruits, seeds, small mammals, amphibians, scraps and will also steal eggs. Crows are scavengers by nature, which is why they tend to frequent sites inhabited by humans in order to feed on their household waste. Crows will also harass birds of prey or even foxes for their kills. Crows actively hunt and occasionally co-operate with other crows to make kills, and are sometimes seen catching ducklings for food. Due to their gregarious lifestyle and defensive abilities, carrion crows have few natural predators. However powerful raptors such as the northern goshawk, the peregrine falcon, the eurasian eagle-owl and the golden eagle will readily hunt them and crows can become an important prey item locally.
The bulky stick nest is usually placed in a tall tree, but cliff ledges, old buildings and pylons may be used as well. Nests are also occasionally placed on or near the ground. The nest resembles that of the common raven, but is less bulky. The 3 to 4 brown-speckled blue or greenish eggs are incubated for 18–20 days by the female alone, who is fed by the male. The young fledge after 29–30 days.
It is not uncommon for an offspring from the previous years to stay around and help rear the new hatchlings. Instead of seeking out a mate, it looks for food and assists the parents in feeding the young.
- BirdLife International (2012). "Corvus corone". IUCN Red List of Threatened Species. IUCN. 2012. Retrieved 26 November 2013.old-form url
- Linnaeus, C (1758). Systema naturae per regna tria naturae, secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis. Tomus I. Editio decima, reformata (in Latin). Holmiae. (Laurentii Salvii). p. 105. Archived from the original on 19 March 2015.
C. atro-caerulescens, cauda rotundata: rectricibus acutis.
- "Corvus". Merriam-Webster online. Retrieved 4 February 2008.
- Liddell & Scott (1980). Greek-English Lexicon, Abridged Edition. Oxford: Oxford University Press. ISBN 978-0-19-910207-5.
- Madge, Steve & Burn, Hilary (1994): Crows and jays: a guide to the crows, jays and magpies of the world. A&C Black, London. ISBN 0-7136-3999-7
- Holden, Peter (2012). RSPB Handbook Of British Birds. p. 274. ISBN 978-1-4081-2735-3.
- Parkin, David T. (2003). "Birding and DNA: species for the new millennium". Bird Study. 50 (3): 223–242. doi:10.1080/00063650309461316.
- Poelstra, Jelmer W.; Vijay, Nagarjun; Bossu, Christen M.; et al. (2014). "The genomic landscape underlying phenotypic integrity in the face of gene flow in crows" (PDF). Science. 344 (6190): 1410–1414. Bibcode:2014Sci...344.1410P. doi:10.1126/science.1253226. ISSN 0036-8075. PMID 24948738.
- de Knijf, Peter (2014). "How carrion and hooded crows defeat Linnaeus's curse". Science. 344 (6190): 1345–1346. Bibcode:2014Sci...344.1345D. doi:10.1126/science.1255744. ISSN 0036-8075. PMID 24948724. Further reading: 
- Attenborough. D. 1998. The Life of Birds. pp.295 BBC ISBN 0563-38792-0
- Pettifor, R. A (1990). "The effects of avian mobbing on a potential predator, the European kestrel, Falco tinnunculus". Animal Behaviour. 39 (5): 821–827. doi:10.1016/S0003-3472(05)80945-5.
- Nieder A.; et al. (2017). "Inside the corvid brain—probing the physiology of cognition in crows". Current Opinion in Behavioral Sciences. 16 (8): 8–14. doi:10.1016/j.cobeha.2017.02.005.
- Ditz, Helen; Nieder, Andreas (2016). "Numerosity representations in crows obey the Weber–Fechner law". Proceedings of the Royal Society B: Biological Sciences. 283 (1827): 20160083. doi:10.1098/rspb.2016.0083. PMC 4822466. PMID 27009227.
- Andreas Nieder; Veit, Lena (28 November 2013). "Abstract rule neurons in the endbrain support intelligent behaviour in corvid songbirds". Nature Communications. 4: 2878. Bibcode:2013NatCo...4.2878V. doi:10.1038/ncomms3878. ISSN 2041-1723. PMID 24285080.
- Wascher, Claudia A. F.; Valdez, Jose W.; Cebrián, Cristina Núñez; Baglione, Vittorio; Canestrari, Daniela (1 January 2014). "Social factors modulating attention patterns in carrion crows". Behaviour. 151 (5): 555–572. doi:10.1163/1568539X-00003148. ISSN 0005-7959.
- Brecht, Katharina F.; Wagener, Lysann; Ostojić, Ljerka; Clayton, Nicola S.; Nieder, Andreas (1 December 2017). "Comparing the face inversion effect in crows and humans". Journal of Comparative Physiology A. 203 (12): 1017–1027. doi:10.1007/s00359-017-1211-7. ISSN 1432-1351. PMC 5696503. PMID 28905251.
- British Trust for Ornithology (2005) Nest Record Scheme data.
- Baglione, V.; Marcos, J. M.; Canestrari, D.; Ekman, J. (2002). "Direct fitness benefits of group living in a complex cooperative society of carrion crows, Corvus corone corone". Animal Behaviour. 64 (6): 887–893. doi:10.1006/anbe.2002.2007.
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