Auk

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Auks
Parakeet Auklets (Aethia psittacula)
Parakeet Auklets (Aethia psittacula)
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Class: Aves
Order: Charadriiformes
Family: Alcidae
Leach, 1820
Genera

Uria
Alle
Alca
Pinguinus
Synthliboramphus
Cepphus
Brachyramphus
Ptychoramphus
Aethia
Cerorhinca
Fratercula
Extinct genera, see Systematics

Auks are birds of the family Alcidae in the order Charadriiformes. They are superficially similar to penguins due to their black-and-white colors, their upright posture and some of their habits. Nevertheless they are not related to the penguins at all, but considered by some to be a product of moderate convergent evolution.

In contrast to penguins, the modern auks are able to fly (with the exception of the recently extinct Great Auk). They are good swimmers and divers, but their walking appears clumsy. Due to their short wings auks have to flap their wings very quickly in order to fly. Extant auks range in size from the Least Auklet, at 85 g (3 oz) and 15 cm (6 inches), to the Thick-billed Murre, at 1 kg (2.2 lbs) and 45 cm (18 inches).

Auks live on the open sea and only go ashore for breeding, although some species, like the Common Guillemot, spend a great part of the year defending their nesting spot from others.

Several species have different names in Europe and North America. The guillemots of Europe are murres in North America, if they occur in both continents, and the Little Auk becomes the Dovekie.

Some species, such as the Uria guillemots, nest in large colonies on cliff edges; others, like the Cepphus guillemots, breed in small groups on rocky coasts; and the puffins, auklets and some murrelets nest in burrows. All species except the Brachyramphus murrelets are colonial.

Feeding and ecology

The feeding behaviour of auks is often compared to that of penguins; they are both wing-propelled pursuit divers. In the region where auks live their only seabird competition is with cormorants (which dive powered by their strong feet); in areas where the two groups feed on the same prey the auks tend to feed further offshore.

Although not to the extent of penguins, auks have to a large extent sacrificed flight, and also mobility on land, in exchange for swimming; their wings are a compromise between the best possible design for diving and the bare minimum needed for flying. This varies by subfamily, the Uria guillemots (including the Razorbill) and murrelets being the most efficient under the water, whereas the puffins and auklets are better adapted for flying and walking. This reflects the type of prey taken; murres hunt faster schooling fish, whereas auklets take slower moving krill. Time depth recorders on auks have shown that they can dive as deep as 100 m in the case of Uria guillemots, 40 m for the Cepphus guillemots and between 30 m for the auklets.


Evolution and distribution

Traditionally, the auks were believed to be one of the earliest distinct charadriiform lineages due to their characteristic morphology. However, molecular analyses have demonstrated that these peculiarities are the product of strong natural selection instead: as opposed to, for example, plovers (a much older charadriiform lineage), auks radically changed from a wading shorebird to a diving seabird lifestyle. Thus, today, the auks are no longer separated in their own suborder ("Alcae"), but are considered part of the Lari suborder which otherwise contains gulls and similar birds. Judging from molecular data, their closest living relatives appear to be the skuas, with these two lineages separating about 30 MYA (Paton et al., 2003). This may or may not be correct due to uncertainties of the fossil record (Thomas et al., 2004, and see below). Alternatively, auks may have split off far earlier from the rest of the Lari and undergone strong morphological, but slow molecular evolution, which would require a very high evolutionary pressure, coupled with a long lifespan and slow reproduction.

The earliest unequivocal fossils of auks are from the Miocene (e.g. the genus Miocepphus, 15 MYA). Two very fragmentary fossils are often assigned to the Alcidae, although this may not be correct: Hydrotherikornis (Late Eocene, some 35 MYA) and Petralca (Late Oligocene). Most extant genera are known to exist since the Late Miocene or Early Pliocene (c. 5 MYA). Miocene fossils have been found in both California and Maryland, but the greater diversity of fossils and tribes in the Pacific leads most scientists to conclude that it was there they first evolved, and it is in the Miocene Pacific that the first fossils of extant genera are found. Early movement between the Pacific and the Atlantic probably happened to the south (since there was no northern opening to the Atlantic), later movements across the Arctic Sea (Konyukhov, 2002). The flightless subfamily Mancallinae which was apparently restricted to the Pacific coast of southern North America became extinct in the Early Pleistocene.

Razorbills are true auks only found in the Atlantic Ocean

The extant auks (subfamily Alcinae) are broken up into 2 main groups: the usually high-billed puffins (tribe Fraterculini) and auklets (tribe Aethiini), as opposed to the more slender-billed murres and true auks (tribe Alcini), and the murrelets and guillemots (tribes Brachyramphini and Cepphini). The tribal arrangement was originally based on analyses of morphology and ecology (Strauch 1985). mtDNA cytochrome b sequence and allozyme studies (Friesen et al., 1996; Moum et al., 2002) confirm these findings except that the Synthliboramphus murrelets should be split into a distinct tribe, as they appear more closely related to the Alcini - in any case, assumption of a closer relationship between the former and the true guillemots was only weakly supported by Strauch's 1985 study.

Compared to other families of seabirds, there are no genera with many species (such as the 47 Larus gulls). This is probably a product of the rather small geographic range of the family (the most limited of any seabird family), and the periods of glacial advance and retreat that have kept the populations on the move in a narrow band of subarctic ocean.

Today, as in the past, the auks are restricted to cooler northern waters. Their ability to spread further south is restricted as their prey hunting method, pursuit diving, becomes less efficient in warmer waters. The speed at which small fish (which along with krill are the auk's principal food items) can swim doubles as the temperature increases from 5°C to 15°C, with no corresponding increase in speed for the bird. The southernmost auks, in California and Mexico, can survive there because of cold upwellings. The current paucity of auks in the Atlantic (6 species), compared to the Pacific (19-20 species) is considered to be because of extinctions to the Atlantic auks; the fossil record shows there were many more species in the Atlantic during the Pliocene. Auks also tend to be restricted to continental shelf waters and breed on few oceanic islands.

Systematics

ORDER CHARADRIIFORMES
Suborder Lari

Family Alcidae

  • Hydrotherikornis (fossil, disputed)
Xantus's Murrelet is a synthliboramphine auk and quite distinct from the brachyramphine murrelets
  • Subfamily Petralcinae (fossil, disputed)
    • Petralca
  • Subfamily Mancallinae (fossil)
    • Alcodes
    • Praemancalla
    • Mancalla
  • Subfamily Alcinae
    • Miocepphus (fossil)
    • Tribe Alcini - Auks and murres
      • Uria
        • Common Guillemot or Common Murre, Uria aalge
        • Brunnich's Guillemot or Thick-billed Murre, Uria lomvia
      • Little Auk or Dovekie, Alle alle
      • Great Auk, Pinguinus impennis (extinct, c.1844)
      • Razorbill, Alca torda
    • Tribe Synthliboramphini - Synthliboramphine murrelets
      Black Guillemot in summer and winter plumages - a true guillemot
      • Synthliboramphus
        • Xantus's Murrelet, Synthliboramphus hypoleucus - sometimes separated in Endomychura
        • Craveri's Murrelet, Synthliboramphus craveri - sometimes separated in Endomychura
        • Ancient Murrelet, Synthliboramphus antiquus
        • Japanese Murrelet, Synthliboramphus wumizusume
    • Tribe Cepphini - True guillemots
      • Cepphus
        • Black Guillemot or Tystie, Cepphus grylle
        • Pigeon Guillemot, Cepphus columba
          • Kurile Guillemot, Cepphus (columba) snowi
        • Spectacled Guillemot, Cepphus carbo
    • Tribe Brachyramphini - Brachyramphine murrelets
      • Brachyramphus
        • Marbled Murrelet, Brachyramphus marmoratus
        • Long-billed Murrelet Brachyramphus perdix
        • Kittlitz's Murrelet, Brachyramphus brevirostris
    • Tribe Aethiini - Auklets
      Tufted Puffin a fraterculine auk
      • Cassin's Auklet, Ptychoramphus aleuticus
      • Aethia
        • Parakeet Auklet, Aethia psittacula
        • Crested Auklet, Aethia cristatella
        • Whiskered Auklet, Aethia pygmaea
        • Least Auklet, Aethia pusilla
    • Tribe Fraterculini - Puffins
      • Rhinoceros Auklet, Cerorhinca monocerata
      • Fratercula
        • Atlantic Puffin, Fratercula arctica
        • Horned Puffin, Fratercula corniculata
        • Tufted Puffin, Fratercula cirrhata

Biodiversity of auks seems to have been markedly higher during the Pliocene (Konyukhov, 2002). See the genus accounts for prehistoric species.

References
ISBN links support NWE through referral fees

  • Collinson, Martin (2006): Splitting headaches? Recent taxonomic changes affecting the British and Western Palaearctic lists. Brit. Birds 99(6): 306-323. HTML abstract
  • Friesen, V. L.; Baker, A. J. & Piatt, J. F. (1996): Phylogenetic Relationships Within the Alcidae (Charadriiformes: Aves) Inferred from Total Molecular Evidence. Molecular Biology and Evolution 13(2): 359-367. PDF fulltext
  • Gaston, Anthony & Jones, Ian (1998): The Auks, Alcidae. Oxford University Press, Oxford. ISBN 0-19-854032-9
  • Konyukhov, N. B. (2002): Possible Ways of Spreading and Evolution of Alcids. Izvestiya Akademii Nauk, Seriya Biologicheskaya 5: 552–560 [Russian version]; Biology Bulletin 29(5): 447–454 [English version]. DOI:10.1023/A:1020457508769 (Biology Bulletin HTML abstract)
  • Moum, Truls; Arnason, Ulfur & Árnason, Einar (2002): Mitochondrial DNA Sequence Evolution and Phylogeny of the Atlantic Alcidae, Including the Extinct Great Auk (Pinguinus impennis). Molecular Biology and Evolution 19(9): 1434–1439. PDF fulltext
  • Paton, T. A.; Baker, A. J.; Groth, J. G. & Barrowclough, G. F. (2003): RAG-1 sequences resolve phylogenetic relationships within charadriiform birds. Molecular Phylogenetics and Evolution 29: 268-278. Digital object identifier (DOI): 10.1016/S1055-7903(03)00098-8 (HTML abstract)
  • Strauch, J. G. Jr. (1985): The phylogeny of the Alcidae. Auk 102(3): 520-539. PDF fulltext

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