| Cormorants and shags |

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| Scientific classification |
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| Species |
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1-8, see text
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| Synonyms |
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Australocorax
Compsohalieus
Euleucocarbo
Halietor
Hypoleucos
Leucocarbo
Microcarbo
Miocorax
Nannopterum
Nesocarbo
Notocarbo
Paracorax
Pliocarbo
Stictocarbo
(but see text)
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The bird family Phalacrocoracidae is today
represented by some 40 species of cormorants and shags. Several different classifications
of the family have been proposed recently, and the number of genera is disputed.
Names
There is no consistent distinction between cormorants and shags. The names "cormorant" and "shag" were originally the common
names of the two species of the family found in Great Britain, Phalacrocorax carbo
(now referred to by ornithologists as the Great Cormorant) and P. aristotelis
(the Common Shag). "Shag" refers to the bird's crest, which the British forms of the Great
Cormorant lack. As other species were discovered by English-speaking sailors and
explorers elsewhere in the world, some were called cormorants and some shags, depending on whether they had crests or not.
Sometimes the same species is called a cormorant in one part of the world and a shag in another, e.g., the Great Cormorant is
called the Black Shag in New Zealand (the birds found in Australasia have a crest that is absent in European members of the species).
Van Tets (1976) proposed to divide the family into two genera and attach the name "Cormorant" to
one and "Shag" to the other, but this flies in the face of common usage and has not been widely adopted.
The scientific genus name is latinized Ancient Greek, from φαλακρός (phalakros, "bald") and κόραξ (korax, "raven").
This is often thought to refer to the creamy white patch on the cheeks of adult Great
Cormorants, or the ornamental white head plumes prominent in Mediterranean birds of this species, but is certainly not a
unifying characteristic of cormorants. "Cormorant" is a contraction derived from
Latin corvus marinus, "sea raven". Indeed, "sea raven" or analogous terms were the usual terms for cormorants in
Germanic languages until after the Middle Ages,
and the erroneous belief that these birds were related to ravens lasted at least to the 16th
century:
"...le bec semblable à celuy d'un cormaran, ou autre corbeau." (..."the beak similar to that of a cormorant or other
corvids."; Thevet, 1558).
Characteristics
Cormorants and shags are medium-to-large seabirds. They range in size from the
Pygmy Cormorant (Phalacrocorax pygmaeus), at as little as 45 cm (18 in) and 340 g
(12 oz), to the Flightless Cormorant (Phalacrocorax harrisi), at a maximum
size 100 cm (40 in) and 5 kg (11 lbs). The recently-extinct Spectacled Cormorant
(Phalacrocorax perspicillatus) was rather larger, at an average size of 6.3 kg (14 lbs). The majority, including nearly
all Northern Hemisphere species, have mainly dark plumage, but some Southern Hemisphere species
are black and white, and a few (e.g. the Spotted Shag of New
Zealand) are quite colourful. Many species have areas of coloured skin on the face (the lores and the gular skin) which can be bright blue, orange, red or yellow,
typically becoming more brightly coloured in the breeding season. The bill is long, thin, and sharply hooked. Their feet have
webbing between all four toes, as in their relatives.
They are coastal rather than oceanic birds, and some have colonised inland waters - indeed, the original ancestor of
cormorants seems to have been a fresh-water bird, judging from the habitat of the most ancient lineage. They range around the
world, except for the central Pacific islands.
All are fish-eaters, dining on small eels, fish, and even water
snakes. They dive from the surface, though many species make a characteristic half-jump as they
dive, presumably to give themselves a more streamlined entry into the water. Under water they propel themselves with their feet.
Some cormorant species have been found, using depth gauges, to dive to depths of as much as
45 metres.
After fishing, cormorants go ashore, and are frequently seen holding their wings out in the sun; it is assumed that this is to
dry them. Unusually for a water bird, their feathers are not waterproofed. This may help them
dive quickly, since their feathers do not retain air bubbles.
Cormorants are colonial nesters, using trees, rocky islets, or cliffs. The eggs are a
chalky-blue colour. There is usually one brood a year. The young are fed through regurgitation. They typically have deep, ungainly bills, showing a greater resemblance to
those of the pelicans', to which they are related, than is obvious in the adults.
Systematics
The cormorants are a group traditionally placed within the Pelecaniformes or, in the
Sibley-Ahlquist taxonomy, the expanded Ciconiiformes. This latter group is certainly not a natural one, and even after the tropicbirds have been recognized as quite distinct, the remaining Pelecaniformes seem not to be entirely
monophyletic. Their relationships and delimitation - apart from being part of a "higher
waterfowl" clade which is similar but not identical to Sibley and Ahlquist's "pan-Ciconiiformes" -
remain mostly unresolved.
Notwithstanding, all evidence agrees that the cormorants and shags are closer to the darters
and Sulidae (gannets and boobies), and perhaps the pelicans
and/or even penguins, than to all other living birds (Kennedy et al. 2000, Mayr 2005). In
recent years, three preferred treatments have emerged: either to leave all living cormorants in a single genus,
Phalacrocorax, or to split off a few species like the Imperial Shag complex
(in Leucocarbo) and perhaps the Flightless Cormorant. Alternatively, the
genus may be disassembled altogether and in the most extreme case be reduced to the Great, White-breasted and Temminck's Cormorants. See Siegel-Causey (1988), Orta (1992) and Kennedy et al. (2000) for a
review of classification schemes.
Pending a thorough review of the Recent and prehistoric cormorants, the single-genus approach of Orta (1992) is followed here
for three reasons: First, it is preferrable to tentatively assigning genera without a robust hypothesis. Second, it makes it
easier to deal with the fossil forms, the systematic treatment of which has been no less controversial than that of living
cormorants and shags. Third, this scheme is also used by the IUCN (2006),
making it easier to incorporate status data. In accordance with the treatment there, the Imperial Shag complex is here left
unsplit too, but the King Shag complex is split up.
Several evolutionary groups are still recognizable. However, combining the available
evidence suggests that there has also been a great deal of convergent evolution;
for example the "cliff shags" are a convergent paraphyletic group. The proposed division into
Phalacrocorax sensu stricto (or subfamily Phalacrocoracinae) "cormorants"
and Leucocarbo sensu lato (or Leucocarboninae) "shags" (van Tets 1976, Siegel-Causey 1988) does indeed have some
degree of merit - though not as originally intended - but fails to account for basal lineages and the fact that the entire family cannot be clearly divided at present beyond the
superspecies or species-complex level (Kennedy et al. 2000). The
resolution provided by the mtDNA 12S rRNA and
ATPase subunits 6 and 8 sequence data of Kennedy et al. (2000) is not sufficient to properly resolve several groups to
satisfaction; in addition, many species remain unsampled, the fossil record has not been integrated in the data, and the effects
of hybridization - known in some Pacific species especially - on the DNA sequence data are
unstudied.
Species in HBW sequence
This sequence follows Orta (1992).
- Double-crested Cormorant or White-crested Cormorant, Phalacrocorax
auritus
- Neotropic Cormorant, Phalacrocorax brasilianus
- Olivaceous Cormorant or Mexican Cormorant, Phalacrocorax olivaceus
- Little Black Cormorant, Phalacrocorax sulcirostris
- Great Cormorant, Phalacrocorax carbo
- White-breasted Cormorant, Phalacrocorax lucidus
- Indian Cormorant, Phalacrocorax fuscicollis
- Cape Cormorant, Phalacrocorax capensis
- Socotra Cormorant, Phalacrocorax nigrogularis
- Wahlberg's Cormorant or Bank Cormorant, Phalacrocorax neglectus
- Temminck's Cormorant or Japanese Cormorant, Phalacrocorax capillatus
- Brandt's Cormorant, Phalacrocorax penicillatus
- Spectacled Cormorant, Phalacrocorax perspicillatus - extinct (c.1850)
- Common Shag, Phalacrocorax aristotelis
- Pelagic Cormorant or Baird's Cormorant, Phalacrocorax pelagicus
- Red-faced Cormorant, Phalacrocorax urile
- Rock Shag, Phalacrocorax magellanicus
- Guanay Cormorant, Phalacrocorax bougainvillii
- Pied Cormorant or Yellow-faced Cormorant, Phalacrocorax varius
- Black-faced Cormorant, Phalacrocorax fuscescens
- King Shag or Rough-faced Shag, Phalacrocorax carunculatus
- Stewart Island Shag, Phalacrocorax chalconotus
- Chatham Shag, Phalacrocorax onslowi
- Auckland Shag, Phalacrocorax colensoi
- Campbell Shag, Phalacrocorax campbelli
- Bounty Shag, Phalacrocorax ranfurlyi
- Imperial Shag or Blue-eyed Shag, Phalacrocorax atriceps
- White-bellied Shag, Phalacrocorax atriceps albiventer
- Antarctic Shag, Phalacrocorax bransfieldensis
- South Georgia Shag, Phalacrocorax georgianus
- Heard Shag, Phalacrocorax nivalis
- Crozet Shag, Phalacrocorax melanogenis
- Kerguelen Shag, Phalacrocorax verrucosus
- Macquarie Shag, Phalacrocorax purpurascens
- Red-footed Shag, Phalacrocorax gaimardi
- Spotted Shag Phalacrocorax punctatus
- Pitt Cormorant or Featherstone's Shag Phalacrocorax featherstoni
- Little Pied Cormorant, Phalacrocorax melanoleucos
- Long-tailed Cormorant, Phalacrocorax africanus
- Crowned Cormorant, Phalacrocorax coronatus
- Little Cormorant, Phalacrocorax niger
- Pygmy Cormorant, Phalacrocorax pygmaeus
- Flightless Cormorant, Phalacrocorax harrisi
Species in phylogenetic sequence
This list attempts to follow a phylogenetic order based on Orta (1992) and Kennedy
et al. (2000). If the distinction into subfamilies would be upheld, the "blue-eyed" and related species would probably be
the Leucocarboninae, and the groups that follow them the Phalacrocoracinae. The first two lineages (and possibly the Flightless
Cormorant) are basal and cannot be assigned to either subfamily.
Basal lineage 1: "Microcormorants", proposed genus Microcarbo or Halietor
("Phalacrocoracinae"); the former genus name would be valid.
- Small, short-billed subtropical to tropical marine and freshwater species from the Old
World and Australia. They have black feet and almost all lack significant white
feathers. They often have a diminutive frontal tuft.
Basal lineage 2: Red-footed Shag. Included in Leucocarbo or Stictocarbo ("Leucocarboninae")
- Pacific coast of South America. This species apparently has no close living relatives.
It has a highly apomorphic color pattern: naked red base of bill, red feet, and a white neck
spot, and it is crestless [1]. It seems to be convergent in some aspects with the punctatus superspecies.[1]
Blue-eyed shags and relatives: variously placed in Euleucocarbo, Hypoleucos Leucocarbo,
Notocarbo and Stictocarbo ("Leucocarboninae")
- This reasonably well-supported marine clade contains 3 lineages:
- One containing American species which are black-footed, black-plumaged, and have vellow skin at the base of the bill as well
as rather inconspicuous crests. They occur in marine and freshwater habitats
- The Rock Shag from southern South America with red skin at the bill base, pink feet, a
frontal crest, and an apomorphic white ear-spot
- A group of numerous close-knit forms from southern Pacific and subantarctic waters
which are white below with pink feet but otherwise quite varying in appearance. It contains the King and Imperial complexes and
the Guanay Cormorant. Almost all have some amount of white on the upperwing coverts, frontal crests, and blue eye-rings. The
crested shags with yellow warts in front of the eyes belong to this group. The genus name Leucocarbo would apply to
either this group, or the entire clade.
- Imperial Shag or Blue-eyed Shag, Phalacrocorax atriceps
- White-bellied Shag, Phalacrocorax (atriceps) albiventer
- Antarctic Shag, Phalacrocorax (atriceps) bransfieldensis
- South Georgian Shag, Phalacrocorax (atriceps) georgianus
- Heard Shag, Phalacrocorax (atriceps) nivalis
- Crozet Shag, Phalacrocorax (atriceps) melanogenis
- Kerguelen Shag, Phalacrocorax (atriceps) verrucosus
- Macquarie Shag, Phalacrocorax (atriceps) purpurascens
- Guanay Cormorant, Phalacrocorax bougainvillii
- King Shag or Rough-faced Shag, Phalacrocorax carunculatus
- Stewart Island Shag, Phalacrocorax chalconotus
- Chatham Shag, Phalacrocorax onslowi
- Auckland Shag, Phalacrocorax colensoi
- Campbell Shag, Phalacrocorax campbelli
- Bounty Shag, Phalacrocorax ranfurlyi
North Pacific shags: spread between Compsohalieus ("Phalacrocoracinae") and Stictocarbo
("Leucocarboninae"). If a distinct genus, the former name would apply
- A well-supported marine group ranging from the Bering Strait to California. They are black-footed and have white ornamental plumes strewn about the head and neck in breeding
plumage. They tend to have prominent double crests.
Common Shag lineage: formerly in Compsohalieus ("Phalacrocoracinae") and Stictocarbo
("Leucocarboninae")
- Black-footed smallish marine shags of Europe and southern Africa. Wahlberg's Cormorant is very tentatively placed here; it
seems anatomically more similar to the P. fuscscens, but the more informative characters - the combination of frontal
crest and lack of extensive naked skin at bill base in mid-sized Old World species - seem to place it here. If this is correct,
they are probably very distantly related due to biogeography.
Indian Ocean group: spread between Hypoleucos and Leucocarbo ("Leucocarboninae") and Compsohalieus
("Phalacrocoracinae"). Hypoleucos would be the correct genus name if they were split off.
- A group of black-footed species occurring in tropical coastal or inland habitat between the
Persian Gulf and Australia. Most species are tentatively assigned here, based on the
combination of range, crestlessness, size, general lack of naked skin ornaments and the presence of some amount of white
feathering in the ear region at least in breeding plumage. This clade is not too well supported, but this may be because the two
presumed members studied by Kennedy et al. (2000) are quite dissimilar; the three unstudied ones are very similar to one
or the other.
Spotted group: placed in Stictocarbo ("Leucocarboninae"); indeed, they would be the only members of this
possibly distinct genus
- A superspecies of the New Zealand region. Peculiarly apomorphic, with yellowish legs,
prominent double crests, white ornamental plumes on the neck, a grey belly and spotted wings.
Cape Cormorant: sometimes placed in Leucocarbo ("Leucocarboninae")
- Highly plesiomorphic among its relatives; a species from the southern coasts of Africa.
It is apparently close to the common ancestor of the next group and, perhaps apart from the all-black plumage, looks almost
identical to that long-extinct bird.
True cormorants: these would be retained in Phalacrocorax no matter how the cormorants and shags are
split up
- They occur from the western Atlantic through the Old World into Australia, usually but not always in marine and temperate to
subtropical habitat. They are characteristic, being large, with white cheek and thigh patches, ornamental plumes in the neck, a
yellow naked bill base, black feet, and a shaggy nape crest.
Incertae sedis: Occasionally placed in the monotypic genus
Nannopterum, alternatively Compsohalieus ("Phalacrocoracinae") or Leucocarbo ("Leucocarboninae")
- The relationships of this species remain unresolved. Confined to the Galapagos
Islands, its wings have evolved to the size of a penguin's flippers. It is extremely apomorphic due to its flightlessness, and its plumage is entirely
nondescript. It might be a derivative of the North Pacific lineage, or even the only cormorant somewhat closer to the Red-footed
Shag.
Evolution and fossil record
Cormorants seem to be a very ancient group, with similar ancestors reaching all the way back to the time of the dinosaurs. In
fact, the very earliest known modern bird, Gansus yumenensis, had essentially the same
structure, although it was not a cormorant per se. The details of the evolution of the cormorant are mostly unknown, today. Even
the technique of using the distribution and relationships of a species to figure out where it came from, biogeography, usually very informative, does not give very specific data for this probably rather ancient
and widespread group.
While the leucocarbonines are almost certainly of southern Pacific origin - possibly even Antarctic, which at the time when cormorants evolved was not yet ice-covered - all that can be said about the
phalacrocoracines is that they are most diverse in the regions bordering the Indian Ocean, but generally occur over a large
area.
Similarly, the origin of the family is shrouded in uncertainties. Some Late
Cretaceous fossils have been proposed to belong into the Phalacrocoracidae:
A scapula from the Campanian-Maastrichtian boundary, about 70 mya, was found in the
Nemegt Formation in Mongolia; it is now in the
PIN collection (Kurochkin 1995). It is from a
bird roughly the size of a Spectacled Cormorant, and quite similar to the
correesponding bone in Phalacrocorax. A Maastrichtian (Late Cretaceous, c.66 mya) right femur, AMNH 25272 from the Lance Formation near Lance Creek, Wyoming, is sometimes
suggested to be the second-oldest record of the Phalacrocoracidae; this was from a rather smaller bird, about the size of a
Long-tailed Cormorant (Hope 2002).
As the Early Oligocene "Sula" ronzoni cannot be assigned to any of the suloid
families - cormorants and shags, darters, and gannets and boobies - with certainty, the best interpretation is that the
Phalacrocoracidae diverged from their closest ancestors in the Early Oligocene, perhaps some 30 million years ago, and that the
Cretaceous fossils represent ancestral suloids, "pelecaniforms" or "higher waterbirds"; at least the last lineage is generally
believed to have been already distinct and undergoing evolutionary radiation at
the end of the Cretaceous. What can be said with certainty
is that AMNH 25272 is from a diving bird that used its feet for underwater locomotion; as this is liable to result in some degree
of convergent evolution and the bone is missing undisputable neornithine features,
it is not entirely certain that the bone is correctly referred to this group (Hope 2002 and see Hesperornithes).
During the late Paleogene, when the family presumably originated, much of Eurasia was
covered by shallow seas, as the Indian Plate finally attached to the mainland. Lacking a
detailed study, it may well be that the first "modern" cormorants were small species from East, Southeast or South Asia, possibly
living in freshwater habitat, that dispersed due to tectonic events. Such a scenario would
account for the present-day distribution of cormorants and shags and is not contradicted by the fossil record; as remarked above,
a thorough review of the problem is not yet available.
One distinct genus of prehistoric cormorants is generally accepted today, if Phalacrocorax is used for all living
species:
- †Nectornis (Late Oligocene?/Early Miocene of C Europe - Middle Miocene of Bes-Konak,
Turkey) - includes Oligocorax miocaenus
The supposed Late Pliocene/Early Pleistocene
"Valenticarbo" is a nomen dubium and
given its recent age probably not a separate genus.
Oligocorax appears to be paraphyletic - the European species have been separated in
Nectornis, and the North Americna ones are placed in the expanded Phalacrocorax. A Late
Oligocene fossil cormoran foot from Enspel (Germany), sometimes placed herein, would then
be referrable to Nectornis if it proves not to be too distinct. All these early European species might belong to the basal
group of "microcormorants", as they agree with them in size and seem to have inhabited the same habitat: subtropical coastal or
inland waters.
The remaining species are, in accordance with the scheme used in this article, all placed in the modern genus
Phalacrocorax:
- Phalacrocorax marinavis (Oligocene ?-? Early Miocene of Oregon, USA) - formerly Oligocorax
- Phalacrocorax littoralis (Early Miocene of St-Gérand-le-Puy, France) - formerly Oligocorax, might belong into
Nectornis
- Phalacrocorax intermedius (Early - Middle Miocene of C Europe) - includes P. praecarbo, Ardea/P. brunhuberi and
Botaurites avitus
- Phalacrocorax macropus (Early Miocene ?-? Pliocene of NW USA)
- Phalacrocorax ibericus (Late Miocene of Valles de Fuentiduena, Spain)
- Phalacrocorax lautus (Late Miocene of Golboçica, Moldavia)
- Phalacrocorax serdicensis (Late Miocene of Hrabarsko, Bulgaria)
- Phalacrocorax femoralis (Modelo Late Miocene/Early Pliocene of WC North America) - formerly Miocorax
- Phalacrocorax sp. (Late Miocene/Early Pliocene of Lee Creek Mine, USA)
- Phalacrocorax longipes (Late Miocene - Early Pliocene of the Ukraine) - formerly Pliocarbo
- Phalacrocorax goletensis (Early Pliocene ?-? Early Pleistocene of Mexico)
- Phalacrocorax wetmorei (Bone Valley Early Pliocene of Florida)
- Phalacrocorax sp. (Bone Valley Early Pliocene of Polk County, USA) - may be P. idahensis
- Phalacrocorax leptopus (Juntura Early/Middle Pliocene of Juntura, USA)
- Phalacrocorax idahensis (Middle Pliocene ?-? Pleistocene of Idaho, USA)
- Phalacrocorax destefanii (Late Pliocene of Italy) - formerly Paracorax
- Phalacrocorax filyawi (Pinecrest Late Pliocene of Florida, USA) - may be P. idahensis
- Phalacrocorax kumeyaay (San Diego Late Pliocene of California)
- Phalacrocorax macer (Late Pliocene of Idaho, USA)
- Phalacrocorax mongoliensis (Late Pliocene of W Mongolia)
- Phalacrocorax rogersi (Late Pliocene -? Early Pleistocene of California, USA)
- Phalacrocorax kennelli (San Diego Pliocene of California)
- Phalacrocorax sp. "Wildhalm" (Pliocene)
- Phalacrocorax chapalensis (Late Pliocene/Early Pleistocene of Jalisco, Mexico
- Phalacrocorax gregorii (Late Pleistocene of Australia) - possibly not a valid species
- Phalacrocorax vetustus (Late Pleistocene of Australia) - formerly Australocorax, possibly not a valid
species
- Phalacrocorax reliquus
- Phalacrocorax sp. (Sarasota County, Florida) - may be P. filawyi/idahensis
The former "Phalacrocorax" (or "Oligocorax") mediterraneus is now considered to belong to the
bathornithid Paracrax antiqua (Cracraft 1971).
Cormorant fishing
Humans have historically exploited cormorants' fishing skills, in China, Japan, and Macedonia, where they have been trained by fishermen. In
Japan, traditional forms of it can be seen on the Nagara River in the city of
Gifu, Gifu Prefecture, where cormorant fishing has continued uninterrupted for 1300 years, or in the city of
Inuyama, Aichi. In Guilin, China, cormorant birds are famous for fishing on the shallow Lijiang
River.
A snare is tied near the base of the bird's throat, which allows the bird only to swallow small fish. When the bird captures
and tries to swallow a large fish, the fish is caught in the bird's throat. When the bird returns to the fisherman's raft, the
fisherman helps the bird to remove the fish from its throat. The method is not as common today, since more efficient methods of
catching fish have been developed.
Cultural references
- Cormorants feature quite commonly in heraldry and medieval ornamentation, usually in their "wing-drying" pose, which was seen as representing the
Christian cross. For example, the Norwegian municipalities of Røst, Loppa and Skjervøy have cormorants in their
coat-of-arms. The species depicted in heraldry is most likely to be the Great Cormorant,
the most familiar species in Europe.
- On the other hand, in Milton's Paradise Lost,
Book IV, Satan takes on the form of a cormorant, sitting on the Tree of Life in form of a
cormorant.
- "Thence up he flew, and on the Tree of Life,
- The middle Tree and highest there that grew,
- Sat like a Cormorant; yet not true Life
- Thereby regaind, but sat devising death
- To them who liv'd; [...]"
-John Milton, Paradise Lost, Book IV, lines 194-98
- Christopher Isherwood was evidently unclear on the differences between
cormorants and shags, and his information about the birds' nesting habits should not be relied on either, as shown in this comic verse.
- In addition to the verse mentioned above, the bird has inspired numerous poets, including Amy
Clampitt, who wrote a poem called "The Cormorant in its Element". (Which species she was
referring to is not obvious, since all members of the family share the characteristic behavioural and morphological features that
the poem celebrates. The combination of "slim head [...] vermilion-strapped" and "big black feet" perhaps points at the
Pelagic Cormorant, which is the only species occurring in the temperate U.S. with
these features.)
- In 1853, a woman wearing a dress made of cormorant feathers was found on San Nicolas
Island, off the southern coast of California. She had sewn the feather dress together
using whale sinews. She is known as the Lone Woman of San Nicolas and was later baptized Juana
María. The woman had lived alone on the island for 18 years before being rescued. The story is the basis for the
Newbery Medal winning novel Island of the
Blue Dolphins, by Scott O'Dell.
- Colin Meloy mentions the cormorant in the song "The Island: Come and See, The Landlord's
Daughter, You'll Not Feel The Drowning" on The Crane Wife, a 2006 album by
the Decemberists.
- In the video game Ace Combat Zero: The Belkan War, the Gelb Squadron
is also known as "The Coupled Cormorants." The callsign of Gelb 2 (2nd Lieutenant Rainer Altman) is "Cormorant." Their squadron
insignia includes a cormorant with goggles.
- In the subbed version of the anime .hack//ROOTS, the character Saburo is quoted as
saying "Now I know how a cormorant feels during cormorant fishing" after she is given a mission without being given a
reason.
- In the film Monty Python's The Meaning of Life, an
assembly of school children are reprimanded as apparently someone had been "rubbing linseed oil into the school cormorant".
- One of the ships named in the first act of Dylan Thomas's Under Milk Wood is named Cormorant.
- In 2005 music group Shriekback released an album titled Cormorant.
- The Moche people of ancient Peru worshipped nature.[2] They placed emphasis on animals and even depicted cormorants in
their art.[3]
References
- Cracraft, Joel (1971): Systematics and evolution of the Gruiformes (Class
Aves). 2. Additional comments on the Bathornithidae, with descriptions of new species. American Museum Novitates
2449: 1-14 PDF fulltext
- Hope, Sylvia (2002): The Mesozoic radiation of Neornithes. In:
Chiappe, Luis M. & Witmer, Lawrence M. (eds.): Mesozoic Birds: Above the Heads
of Dinosaurs: 339-388. ISBN 0520200942
- IUCN & Species Survival Commission (2006): 2006 IUCN Red List of Threatened Species. IUCN,
Gland.
- Kennedy, M.; Gray, R.D. & Spencer H.G. (2000): The Phylogenetic
Relationships of the Shags and Cormorants: Can Sequence Data Resolve a Disagreement between Behavior and Morphology? Molecular
Phylogenetics and Evolution 17(3): 345-359. doi:10.1006/mpev.2000.0840 PDF fulltext
- Kurochkin, Evgeny N. (1995): Synopsis of Mesozoic birds and early evolution of
Class Aves. Archaeopteryx 13: 47–66. PDF fulltext
- Mayr, Gerald (2005): Tertiary plotopterids (Aves, Plotopteridae) and a novel
hypothesis on the phylogenetic relationships of penguins (Spheniscidae). Journal of Zoological Systematics 43(1):
67-71. PDF fulltext
- Orta, Jaume (1992): Family Phalacrocoracidae. In: del Hoyo, Josep; Elliott, Andrew & Sargatal, Jordi (eds.): Handbook of Birds of the World, Volume 1 (Ostrich to Ducks): 326-353, plates
22-23. Lynx Edicions, Barcelona. ISBN 84-87334-10-5
- Siegel-Causey, Douglas (1988): Phylogeny of the Phalacrocoracidae.
Condor 90(4): 885–905. PDF
fulltext
- Thevet, F. André (1558): [About birds of Ascension Island]. In: Les
singularitez de la France Antarctique, autrement nommee Amerique, & de plusieurs terres & isles decouvertes de nostre
temps: 39-40. Maurice de la Porte heirs, Paris. Fulltext at Gallica
- van Tets, G. F. (1976): Australasia and the origin of shags and cormorants,
Phalacrocoracidae. Proceedings of the XVI International Ornithological Congress: 121–124.
Footnotes
- ^ Much of Phalacrocoracidae systematics hinges upon this most enigmatic
species. The white neck spots and general coloration are very much unlike that of any other living cormorant, though
anatomically it is quite similar to the species composing the punctatus superspecies,
which are also the only other members of this family with a grey background color. No satisfying theory has been proposed to
explain this oddity. What seems sure by now is that this species must be placed in a distinct monotypic genus in almost any case, if species are split from Phalacrocorax.
- ^ Benson, Elizabeth, The Mochica: A Culture of Peru. New York, NY: Praeger
Press. 1972
- ^ Berrin, Katherine & Larco Museum. The Spirit of Ancient
Peru:Treasures from the Museo Arqueológico Rafael Larco Herrera. New York:
Thames and Hudson, 1997.
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