Bird of prey

Birds of prey
Birds of prey (or "raptors") are not a taxon, they are an informal grouping of predatory members of Telluraves

Golden eagle (Aquila chrysaetos)
Information
Orders and families of birds of prey

Bird of prey or predatory bird, also known as raptors, refers to several species of birds that hunt and feed on rodents and other small animals. The term raptor is derived from the Latin word rapere, meaning to seize or take by force.[1] These birds are characterized by keen vision that allows them to detect their prey during flight and powerful talons and beaks.

Taken literally, the term bird of prey has a wide meaning that includes many birds that hunt and feed on animals and also birds that eat very small insects.[2] In ornithology, the definition for "bird of prey" has a narrower meaning: birds that have very good eyesight for finding food, strong feet for holding food, and a strong curved beak for tearing flesh.[3] Most birds of prey also have strong curved talons for catching or killing prey.[3][4] An example of this difference in definition, the narrower definition excludes storks and gulls, which can eat quite large fish, partly because these birds catch and kill prey entirely with their beaks,[2] and similarly bird-eating skuas, fish-eating penguins, and vertebrate-eating kookaburras are excluded. Birds of prey generally prey on vertebrates, which are usually quite large relative to the size of the bird.[2] Most also eat carrion, at least occasionally, and vultures and condors eat carrion as their main food source.[3]

Common names

The common names for various birds of prey are based on structure, but many of the traditional names do not reflect the evolutionary relationships between the groups.

Variations in shape and size

Many of these English language group names originally referred to particular species encountered in Britain. As English-speaking people travelled further, the familiar names were applied to new birds with similar characteristics. Names that have generalised this way include: kite (Milvus milvus), sparrow-hawk or sparhawk (Accipiter nisus), goshawk (Accipiter gentilis), kestrel (Falco tinninculus), hobby (Falco subbuteo), harrier (simplified from "hen-harrier", Circus cyaneus), buzzard (Buteo buteo).

Some names have not generalised, and refer to single species (or groups of closely related (sub)species): merlin (Falco columbarius), osprey (Pandion haliaetus).

Systematics

Historical classifications

The taxonomy of Carl Linnaeus grouped birds (class Aves) into orders, genera, and species, with no formal ranks between genus and order. He placed all birds of prey into a single order, Accipitres, subdividing this into four genera: Vultur (vultures), Falco (eagles, hawks, falcons, etc.), Strix (owls), and Lanius (shrikes). This approach was followed by subsequent authors such as Gmelin, Latham, and Turnton.

Louis Pierre Veillot used additional ranks: order, tribe, family, genus, species. Birds of prey (order Accipitres) were divided into diurnal and nocturnal tribes; the owls remained monogeneric (family Ægolii, genus Strix), whilst the diurnal raptors were divided into three families: Vulturini, Gypaëti, and Accipitrini.[5]

Thus Veillot's families were similar to the Linnaean genera, with the difference that shrikes were no longer included amongst the birds of prey. In addition to the original Vultur and Falco (now reduced in scope), Veillot adopted four genera from Savigny: Phene, Haliæetus, Pandion, and Elanus. He also introduced five new genera of vultures (Gypagus, Catharista, Daptrius, Ibycter, Polyborus)[note 1] and eleven new genera of accipitrines (Aquila, Circaëtus, Circus, Buteo, Milvus, Ictinia, Physeta, Harpia, Spizaëtus, Asturina, Sparvius).

Modern systematics

The order Accipitriformes is believed to have originated 44 million years ago when it split from the common ancestor of the secretarybird (Sagittarius serpentarius) and the accipitrid species.[6] The phylogeny of Accipitriformes is complex and difficult to unravel. Widespread paraphylies were observed in many phylogenetic studies.[7][8][9][10][11] More recent and detailed studies show similar results.[12] However, according to the findings of a 2014 study, the sister relationship between larger clades of Accipitriformes was well supported (e.g. relationship of Harpagus kites to buzzards and sea eagles and these latter two with Accipiter hawks are sister taxa of the clade containing Aquilinae and Harpiinae).[6]

The diurnal birds of prey are formally classified into five families of two orders.

These families were traditionally grouped together in a single order Falconiformes but are now split into two orders, the Falconiformes and Accipitriformes. The Cathartidae are sometimes placed separately in an enlarged stork family, Ciconiiformes, and may be raised to an order of their own, Cathartiiformes.

The secretary bird and/or osprey are sometimes listed as subfamilies of Acciptridae: Sagittariinae and Pandioninae, respectively.

Australia's letter-winged kite is a member of the family Accipitridae, although it is a nocturnal bird.

The nocturnal birds of prey – the owls – are classified separately as members of two extant families of the order Strigiformes:

Phylogeny

Below is a simplified phylogeny of Telluraves which is the clade where the birds of prey belong to along with passerines and several near-passerine lineages.[13][14][15] The orders that bolden in text are birds of prey orders; this is to show the polyphly of the group as well as showing their relationships to other birds.

Telluraves

Afroaves

Accipitrimorphae


Accipitriformes (hawks and relatives)



Cathartiformes (New World vultures)





Strigiformes (owls)



Coraciimorphae (woodpeckers, rollers, hornbills, etc.)




Australaves


Cariamiformes (seriemas)


Eufalconimorphae


Falconiformes (falcons)



Psittacopasserae (parrots and songbirds)





Migration

Migratory behaviour evolved multiple times within accipitrid raptors.

An obliged point of transit of the migration of the birds of prey is the bottleneck-shaped Strait of Messina, Sicily, here seen from Dinnammare mount, Peloritani.

The earliest event occurred nearly 14 to 12 million years ago. This result seems to be one of the oldest dates published so far in the case of birds of prey.[6] For example, a previous reconstruction of migratory behaviour in one Buteo clade[11] with a result of the origin of migration around 5 million years ago was also supported by that study.

Migratory species of raptors had a southern origin because it seems that all of the major lineages within Accipitridae had an origin to one of the biogeographic realms of the Southern Hemisphere. The appearance of migratory behaviour occurred in the tropics parallel with the range expansion of migratory species to temperate habitats.[6] Similar results of southern origin in other taxonomic groups can be found in the literature.[16][17][18]

Distribution and biogeographic history highly determine the origin of migration in birds of prey. Based on some comparative analyses, diet breadth also has an effect on the evolution of migratory behaviour in this group,[6] but its relevance needs further investigation. The evolution of migration in animals seems to be a complex and difficult topic with many unanswered questions.

A recent study discovered new connections between migration and the ecology, life history of raptors. A brief overview from abstract of the publish paper shows that "clutch size and hunting strategies have been proved to be the most important variables in shaping distribution areas, and also the geographic dissimilarities may mask important relationships between life history traits and migratory behaviours. The West Palearctic-Afrotropical and the North-South American migratory systems are fundamentally different from the East Palearctic-Indomalayan system, owing to the presence versus absence of ecological barriers."[19] Maximum entropy modelling can help in answering the question: why species winters at one location while the others are elswhere. It is interesting that how temperature and precipitation related factors differs in the limitation of species distributions. "This suggests that the migratory behaviours differ among the three main migratory routes for these species"[19] which may have important consevational consequences in the protection of migratory raptors.

Sexual dimorphism

Shikra female has yellow eye

Raptors are known to display patterns of sexual dimorphism. It is commonly believed that the dimorphisms found in raptors occur due to sexual selection or environmental factors. In general, hypotheses in favor of ecological factors being the cause for sexual dimorphism in raptors are rejected. This is because the ecological model is less parsimonious, meaning that its explanation is more complex than that of the sexual selection model. Additionally, ecological models are much harder to test because a great deal of data is required.[20]

Dimorphisms can also be the product of intrasexual selection between males and females. It appears that both sexes of the species play a role in the sexual dimorphism within raptors; females tend to compete with other females to find good places to nest and attract males, and males competing with other males for adequate hunting ground so they appear as the most healthy mate.[21] It has also been proposed that sexual dimorphism is merely the product of disruptive selection, and is merely a stepping stone in the process of speciation, especially if the traits that define gender are independent across a species. Sexual dimorphism can be viewed as something that can accelerate the rate of speciation.[22]

In non-predatory birds, males are typically larger than females. However, in birds of prey, the opposite is the case. For instance, the kestrel is a type of falcon in which males are the primary providers, and the females are responsible for nurturing the young. In this species, the smaller the kestrels are, the less food is needed and thus, they can survive in environments that are harsher. This is particularly true in the male kestrels. It has become more energetically favorable for male kestrels to remain smaller than their female counterparts because smaller males have an agility advantage when it comes to defending the nest and hunting. Larger females are favored because they can incubate larger numbers of offspring, while also being able to breed a larger clutch size.[23]

See also

Notes

  1. Veillot included the caracaras (Daptrius, Ibycter, and Polyborus) in Vulturini, though it is now known that they are related to falcons.

References

  1. Brown, Leslie (1997). Birds of Prey. Chancellor Press. ISBN 1-85152-732-X.
  2. 1 2 3 Burton, Philip (1989). Birds of Prey. illustrated by Boyer, Trevor; Ellis, Malcolm; Thelwell, David. Gallery Books. p. 8. ISBN 0-8317-6381-7.
  3. 1 2 3 Perrins, Christopher, M; Middleton, Alex, L. A., eds. (1984). The Encyclopaedia of Birds. Guild Publishing. p. 102.
  4. Fowler, D.W.; Freedman, E.A.; & Scannella, J.B. (2009). "Predatory Functional Morphology in raptors: Interdigital Variation in Talon Size Is Related to Prey Restraint and Immobilisation Technique". PLoS ONE. 4 (11): e7999. PMC 2776979Freely accessible. PMID 19946365. doi:10.1371/journal.pone.0007999.
  5. Veillot, Louis Pierre (1816). Saunders, Howard, ed. Analyse d'une nouvelle ornithologie élémentaire. (in French) (London 1883 ed.). Willughby Society.
  6. 1 2 3 4 5 Nagy, J.; Tökölyi, J. (2014). "Phylogeny, historical biogeography and the evolution of migration in accipitrid birds of prey (Aves: Accipitriformes)" (PDF). Ornis Hungarica. 22 (1): 15–35. doi:10.2478/orhu-2014-0008.
  7. Motta-Junior, et. al. (eds.) (2004). Raptors worldwide (PDF). Berlin: WWGBP. pp. 483–498.
  8. Helbig, A. J.; Kocum, A.; Seibold, I.; Braun, M. J. (2005). "A multi-gene phylogeny of aquiline eagles (Aves: Accipitriformes) reveals extensive paraphyly at the genus level". Molecular Phylogenetics and Evolution. 35 (1): 147–164. PMID 15737588. doi:10.1016/j.ympev.2004.10.003.
  9. Lerner, H. R. L.; Mindell, D. P. (2005). "Phylogeny of eagles, Old World vultures, and other Accipitridae based on nuclear and mitochondrial DNA" (PDF). Molecular Phylogenetics and Evolution. 37 (2): 327–346. PMID 15925523. doi:10.1016/j.ympev.2005.04.010.
  10. Griffiths, C. S.; Barrowclough, G. F.; Groth, J. G.; Mertz, L. A. (2007). "Phylogeny, diversity, and classification of the Accipitridae based on DNA sequences of the RAG-1 exon". Journal of Avian Biology. 38 (5): 587–602. doi:10.1111/j.2007.0908-8857.03971.x.
  11. 1 2 do Amaral, F. R., et. al. (2009). "Patterns and processes of diversification in a widespread and ecologically diverse avian group, the buteonine hawks (Aves, Accipitridae)" (PDF). Molecular Phylogenetics and Evolution. 53 (3): 703–715. PMID 19635577. doi:10.1016/j.ympev.2009.07.020.
  12. Breman, F. C., et. al. (2013). "DNA barcoding and evolutionary relationships in Accipiter Brisson, 1760 (Aves, Falconiformes: Accipitridae) with a focus on African and Eurasian representatives.". Journal of Ornithology. 154 (1): 265–287. doi:10.1007/s10336-012-0892-5.
  13. Yuri, T.; et al. (2013). "Parsimony and Model-Based Analyses of Indels in Avian Nuclear Genes Reveal Congruent and Incongruent Phylogenetic Signals". Biology. 2 (1): 419–444. PMC 4009869Freely accessible. PMID 24832669. doi:10.3390/biology2010419.
  14. Ericson, P. G. (2012). "Evolution of terrestrial birds in three continents: biogeography and parallel radiations" (PDF). Journal of Biogeography. 39 (5): 813–824. doi:10.1111/j.1365-2699.2011.02650.x.
  15. Jarvis, E. D.; Mirarab, S.; Aberer, A. J.; Li, B.; Houde, P.; Li, C.; Ho, S. Y. W.; Faircloth, B. C.; Nabholz, B.; Howard, J. T.; Suh, A.; Weber, C. C.; Da Fonseca, R. R.; Li, J.; Zhang, F.; Li, H.; Zhou, L.; Narula, N.; Liu, L.; Ganapathy, G.; Boussau, B.; Bayzid, M. S.; Zavidovych, V.; Subramanian, S.; Gabaldon, T.; Capella-Gutierrez, S.; Huerta-Cepas, J.; Rekepalli, B.; Munch, K.; et al. (2014). "Whole-genome analyses resolve early branches in the tree of life of modern birds" (PDF). Science. 346 (6215): 1320–1331. PMC 4405904Freely accessible. PMID 25504713. doi:10.1126/science.1253451.
  16. Joseph, L.; Lessa, E. P.; Christidis, L. (1999). "Phylogeny and biogeography in the evolution of migration: shorebirds of the Charadrius complex". Journal of Biogeography. 26 (2): 329–342. doi:10.1046/j.1365-2699.1999.00269.x.
  17. Outlaw, D. C., et. al. (2003). "Evolution of long-distance migration in and historical biogeography of Catharus thrushes: a molecular phylogenetic approache". The Auk. 120: 299–310. doi:10.1642/00048038(2003)120[0299:EOLMIA]2.0.CO;2.
  18. Milá, B.; Smith, T. B.; Wayne, R. K. (2006). "Postglacial population expansion drives the evolution of long–distance migration in a songbird". Evolution. 60 (11): 2403–2409. PMID 17236431. doi:10.1111/j.0014-3820.2006.tb01875.x.
  19. 1 2 Nagy,, Jenő; Végvári,, Zsolt; Varga,, Zoltán (2016). "Life history traits, bioclimate, and migratory systems of accipitrid birds of prey (Aves: Accipitriformes)". Biological Journal of the Linnean Society. 121: 63–71. doi:10.1093/biolinnean/blw021.
  20. Mueller, H.C. "The Evolution of Reversed Sexual Dimorphism in Owls: An Empirical Analysis of Possible Selective Factors". The Wilson Bulletin. 98 (3): 387–406.
  21. Wiehn, J.; Korpimakki, E.; Massemin, S. (2000). "Reversed sexual size dimorphism in raptors: evaluation of the hypotheses in kestrels breeding in a temporally changing environment". Oecologia. 124: 26–32.
  22. BOLNICK, David; DOEBEL, Michael (November 2003). "SEXUAL DIMORPHISM AND ADAPTIVE SPECIATION: TWO SIDES OF THE SAME ECOLOGICAL COIN". The society of evolution. 57 (11).
  23. Sonerud, G; Steen, R; Low, L; Roed, L.; Skar, K.; Selas, V; Slagsvold, T (2013). "Size-biased allocation of prey from male to offspring via female: family conflicts, prey selection, and evolution of sexual size dimorphism in raptors". Oceologa. 172 (1): 93–107. doi:10.1007/s00442-012-2491-9.

Further reading

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