Cormorant

Phalacrocoracidae is a family of approximately 40 species of aquatic birds commonly known as cormorants and shags. Several different classifications of the family have been proposed, but in 2021 the International Ornithologists' Union (IOU) adopted a consensus taxonomy of seven genera.[1] The great cormorant (Phalacrocorax carbo) and the common shag (Gulosus aristotelis) are the only two species of the family commonly encountered in Britain and Ireland[2] and "cormorant" and "shag" appellations have been later assigned to different species in the family somewhat haphazardly.

For other uses, see Cormorant (disambiguation).

Cormorants and shags
Temporal range: Late Oligocene - present
Little pied cormorant
Microcarbo melanoleucos
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Clade: Dinosauria
Class: Aves
Order: Suliformes
Family: Phalacrocoracidae
Reichenbach, 1850
Type genus
Phalacrocorax
Genera

Microcarbo
Poikilocarbo
Urile
Phalacrocorax
Gulosus
Nannopterum
Leucocarbo

Synonyms

Australocorax Lambrecht, 1931
Compsohalieus B. Brewer & Ridgway, 1884
Cormoranus Baillon, 1834
Dilophalieus Coues, 1903
Ecmeles Gistel, 1848
Euleucocarbo Voisin, 1973
Halietor Heine, 1860
Hydrocorax Vieillot, 1819 (non Brisson, 1760: preoccupied)
Hypoleucus Reichenbach, 1852
Miocorax Lambrecht, 1933
Nesocarbo Voisin, 1973
Notocarbo Siegel-Causey, 1988
Pallasicarbo Coues, 1903
Paracorax Lambrecht, 1933
Pliocarbo Tugarinov, 1940
Stictocarbo Bonaparte, 1855
Viguacarbo Coues, 1903
Anatocarbo
Nanocorax
(see text)

Cormorants and shags are medium-to-large birds, with body weight in the range of 0.35–5 kilograms (0.77–11.02 lb) and wing span of 60–100 centimetres (24–39 in). The majority of species have dark feathers. The bill is long, thin and hooked. Their feet have webbing between all four toes. All species are fish-eaters, catching the prey by diving from the surface. They are excellent divers, and under water they propel themselves with their feet with help from their wings; some cormorant species have been found to dive as deep as 45 metres (150 ft). They have relatively short wings due to their need for economical movement underwater, and consequently have among the highest flight costs of any flying bird.[3]

Cormorants nest in colonies around the shore, on trees, islets or cliffs. They are coastal rather than oceanic birds, and some have colonised inland waters. The original ancestor of cormorants seems to have been a fresh-water bird. They range around the world, except for the central Pacific islands.

Names

"Cormorant" is a contraction derived either directly from Latin corvus marinus, "sea raven", or through Brythonic Celtic. Cormoran is the Cornish name of the sea giant in the tale of Jack the Giant Killer. Indeed, "sea raven" or analogous terms were the usual terms for cormorants in Germanic languages until after the Middle Ages. The French explorer André Thévet commented in 1558: "the beak [is] similar to that of a cormorant or other corvid", which demonstrates that the erroneous belief that the birds were related to ravens lasted at least to the 16th century.

No consistent distinction exists 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 Gulosus aristotelis (the European shag). "Shag" refers to the bird's crest, which the British forms of the great cormorant lack. As other species were encountered by English-speaking sailors and explorers elsewhere in the world, some were called cormorants and some shags, sometimes 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; for example, all species in the family which occur in New Zealand are known locally as shags, including four non-endemic species known as cormorant elsewhere in their range. 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 nomenclature has not been widely adopted.

Description
Great cormorant with hooked bill
Little cormorant with wings spread

Cormorants and shags are medium-to-large seabirds. They range in size from the pygmy cormorant (Microcarbo pygmaeus), at as little as 45 cm (18 in) and 340 g (12 oz), to the flightless cormorant (Nannopterum harrisi), at a maximum size 100 cm (39 in) and 5 kg (11 lb). The recently extinct spectacled cormorant (Urile perspicillatus) was rather larger, at an average size of 6.3 kg (14 lb). 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.

Habitat
Imperial shags in Beagle Channel

Habitat varies from species to species: some are restricted to seacoasts, while others occur in both coastal and inland waters to varying degrees. They range around the world, except for the central Pacific islands.

Behaviour

All cormorants and shags 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, though some also propel themselves with their wings (see the picture,[4] commentary,[5] and existing reference video[6]). Imperial shags fitted with miniaturized video recorders have been filmed diving to depths of as much as 80 metres (260 ft) to forage on the sea floor.[7]

Wing-drying behaviour in a little cormorant

After fishing, cormorants go ashore, and are frequently seen holding their wings out in the sun. All cormorants have preen gland secretions that are used ostensibly to keep the feathers waterproof. Some sources[8] state that cormorants have waterproof feathers while others say that they have water-permeable feathers.[9][10] Still others suggest that the outer plumage absorbs water but does not permit it to penetrate the layer of air next to the skin.[11] The wing drying action is seen even in the flightless cormorant but not in the Antarctic shags[12] or red-legged cormorants. Alternate functions suggested for the spread-wing posture include that it aids thermoregulation[13] or digestion, balances the bird, or indicates presence of fish. A detailed study of the great cormorant concludes that it is without doubt[14] to dry the plumage.[15][16]

Cormorants are colonial nesters, using trees, rocky islets, or cliffs. The eggs are a chalky-blue colour. There is usually one brood a year. Parents regurgitate food to feed their young.

Taxonomy

The genus Phalacrocorax, from which the family name Phalacrocoracidae is derived, is Latinised from Ancient Greek φαλακρός phalakros "bald" and κόραξ korax "raven".[17] 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.

The cormorant family are a group traditionally placed within the Pelecaniformes or, in the Sibley–Ahlquist taxonomy of the 1990s, the expanded Ciconiiformes. Pelecaniformes in the traditional sense—all waterbird groups with totipalmate foot webbing—are not a monophyletic group, even after the removal of the distantly-related tropicbirds. 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 or even penguins, than to all other living birds.[18]

In recent years, three preferred treatments of the cormorant family have emerged: either to leave all living cormorants in a single genus, Phalacrocorax, or to split off a few species such as 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 Japanese cormorants.[19] In 2014, a landmark study proposed a 7 genera treatment, which was adopted by the IUCN Red List and BirdLife International, and later by the IOC in 2021, standardizing it.[1][20]

Occipital crest or os nuchale in Phalacrocorax carbo

The cormorants and the darters have a unique bone on the back of the top of the skull known as the os nuchale or occipital style which was called a xiphoid process in early literature. This bony projection provides anchorage for the muscles that increase the force with which the lower mandible is closed.[21][22] This bone and the highly developed muscles over it, the M. adductor mandibulae caput nuchale, are unique to the families Phalacrocoracidae and Anhingidae.[23][24]

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[25] does have some degree of merit.[26] The resolution provided by the mtDNA 12S rRNA and ATPase subunits six and eight sequence data[26] 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 hybridisation – known in some Pacific species especially – on the DNA sequence data are unstudied.

A multigene molecular phylogenetic study published in 2014 provided a genus-level phylogeny of the family.[20]

Phalacrocoracidae

Microcarbo – 5 species

Poikilocarbo – red-legged cormorant

Urile – 4 species

Phalacrocorax – 12 species

Gulosus – European shag

Nannopterum – 3 species

Leucocarbo – 16 species

List of genera
Cormorant (species unknown) begins its dive
Immature imperial shag (Leucocarbo atriceps)
Little cormorant (Microcarbo niger) in Hyderabad, India
Guanay cormorant (Leucocarbo bougainvillii) at Weltvogelpark Walsrode

As per the IOU, the IUCN Red List and BirdLife International, the family contains 7 genera:[1]

ImageGenusSpecies
Microcarbo Bonaparte, 1856

Around Indian Ocean, one species extending from Central Asia into Europe. Mostly in freshwater habitat. Small (about 50-60 cm long), nondescript black to dark brown (except for one species with white underparts).

Poikilocarbo Boetticher, 1935

Subtropical to subantarctic Pacific South America, ranging a bit into the southwestern Atlantic. Maritime. Mid-sized (around 75 cm), grey with scalloped wings and contrasting white/yellow/red neck mark and bare parts. Its high-pitched chirping calls are quite unlike those of other cormorants.

Urile Bonaparte, 1855

Northern Pacific, one species extending into subtropical waters on the American West Coast. Maritime. Smallish to large (65-100 cm), generally black with metallic sheen (usually blue/green), in breeding plumage with bright bare facial skin in the eye region and two crests (crown and nape).

Phalacrocorax Brisson, 1760

Mostly around Indian Ocean, one species group extending throughout Eurasia and to Atlantic North America. Maritime to freshwater. Size very variable (60-100 cm), blackish with metallic sheen (usually bronze to purple) and/or white cheek and thigh patches or underside at least in breeding plumage; usually a patch of bare yellow skin at the base of the bill.

Gulosus Montagu, 1813

Breeds in European Arctic, winters in Europe and North Africa. Maritime. Mid-sized (70-80 cm), glossy black, in breeding plumage with a forehead crest curled to the front.

Nannopterum Sharpe, 1899

Throughout the Americas. Mostly freshwater. Smallish to large (65-100 cm), nondescript brownish-black. One species with white tufts on sides of head in breeding plumage.

Leucocarbo Bonaparte, 1856

Generally Subantarctic, but extending farther north in South America; many oceanic-island endemics. Maritime. Smallish to largish (65-80 cm), typically black above, white below, and with bare yellow or red skin in the facial region. A circumpolar group of several species (the blue-eyed shag complex) is characterised by bright blue orbital skin.

Prior to 2021, the IOU (or formerly the IOC) classified all these species in just three genera: Microcarbo, Leucocarbo, and a broad Phalacrocorax containing all remaining species; however, this treatment rendered Phalacrocorax deeply paraphyletic with respect to Leucocarbo. Other authorities, such as the Clements Checklist, formerly recognised only Microcarbo as a separate genus from Phalacrocorax.

For details, see the article "List of cormorant species".

Evolution and fossil record

The details of the evolution of the cormorants are mostly unknown. 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. However, the closest living relatives of the cormorants and shags are the other families of the suborder Sulae—darters and gannets and boobies—which have a primarily Gondwanan distribution. Hence, at least the modern diversity of Sulae probably originated in the southern hemisphere.

While the Leucocarbonines are almost certainly of southern Pacific origin—possibly even the 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 with the Phalacrocoracidae:
A scapula from the Campanian-Maastrichtian boundary, about 70 mya (million years ago), was found in the Nemegt Formation in Mongolia; it is now in the PIN collection.[27] It is from a bird roughly the size of a spectacled cormorant, and quite similar to the corresponding bone in Phalacrocorax. A Maastrichtian (Late Cretaceous, c. 66 mya) right femur, AMNH FR 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.[28] However, cormorants likely originated much later, and these are likely misidentifications.[29]

As the Early Oligocene "Sula" ronzoni cannot be assigned to any of the sulid 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 sulids, "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 near certainty is that AMNH FR 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 indisputable neornithine features, it is not entirely certain that the bone is correctly referred to this group.[30]

Phylogenetic evidence indicates that the cormorants diverged from their closest relatives, the darters, during the Late Oligocene, indicating that most of the claims of Cretaceous or early Paleogene cormorant occurrences are likely misidentifications.[29]

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 eastern, south-eastern or southern 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.

Double-crested cormorant

Even when Phalacrocorax was used to unite all living species, two distinct genera of prehistoric cormorants became widely accepted today:

  • Limicorallus (Indricotherium middle Oligocene of Chelkar-Teniz, Kazakhstan)
  • Nectornis (Late Oligocene/Early Miocene of Central Europe – Middle Miocene of Bes-Konak, Turkey) – includes Oligocorax miocaenus

The proposed genus Oligocorax appears to be paraphyletic – the European species have been separated in Nectornis, and the North American ones placed in the expanded Phalacrocorax; the latter might just as well be included in Nannopterum. A Late Oligocene fossil cormorant foot from Enspel, Germany, sometimes placed in Oligocorax, would then be referable to Nectornis if it proves not to be too distinct. Limicorallus, meanwhile, was initially believed to be a rail or a dabbling duck by some. There are also undescribed remains of apparent cormorants from the Quercy Phosphorites of Quercy (France), dating to some time between the Late Eocene and the mid-Oligocene. All these early European species might belong to the basal group of "microcormorants", as they conform with them in size and seem to have inhabited the same habitat: subtropical coastal or inland waters. While this need not be more than convergence, the phylogeny of the modern (sub)genus Microcarbo – namely, whether the Western Eurasian M. pygmaeus is a basal or highly derived member of its clade – is still not well understood at all as of 2022.

Some other Paleogene remains are sometimes assigned to the Phalacrocoracidae, but these birds seem rather intermediate between cormorants and darters (and lack clear autapomorphies of either). Thus, they may be quite basal members of the Palacrocoracoidea. The taxa in question are:

  • Piscator (Late Eocene of England)
  • "Pelecaniformes" gen. et sp. indet. (Jebel Qatrani Early Oligocene of Fayum, Egypt) – similar to Piscator?
  • Borvocarbo (Late Oligocene of C Europe)

The supposed Late Pliocene/Early Pleistocene "Valenticarbo" is a nomen dubium and given its recent age probably not a separate genus.

The remaining fossil species are not usually placed in a modern phylogenetic framework. While the numerous western US species are most likely prehistoric representatives of the coastal Urile or inland Nannopterum, the European fossils pose much more of a problem due to the singular common shag being intermediate in size between the other two European cormorant lineages, and as of 2022 still of mysterious ancestry; notably, a presumably lost collection of Late Miocene fossils from the Odesa region may have contained remains of all three (sub)genera inhabiting Europe today. Similarly, the Plio-Pleistocene fossils from Florida have been allied with Nannopterum and even Urile, but may conceivably be Phalacrocorax; they are in serious need of revision since it is not even clear how many species are involved. Provisionally, the fossil species are thus all placed in Phalacrocorax here:

  • Phalacrocorax marinavis (Oligocene – Early Miocene of Oregon, US) – formerly Oligocorax; Urile or Nannopterum?
  • Phalacrocorax littoralis (Late Oligocene/Early Miocene of St-Gérand-le-Puy, France) – formerly Oligocorax; Nectornis?
  • Phalacrocorax intermedius (Early – Middle Miocene of C Europe) – includes P. praecarbo, Ardea/P. brunhuberi and Botaurites avitus; Microcarbo, Phalacrocorax or Gulosus?
  • Phalacrocorax macropus (Early Miocene – Pliocene of north-west US) – Urile or Nannopterum?
  • Phalacrocorax ibericus (Late Miocene of Valles de Fuentiduena, Spain) – Microcarbo, Phalacrocorax or Gulosus?
  • Phalacrocorax lautus (Late Miocene of Golboçica, Moldavia) – Microcarbo, Phalacrocorax or Gulosus?
  • Phalacrocorax serdicensis (Late Miocene of Hrabarsko, Bulgaria); Microcarbo, Phalacrocorax or Gulosus?
  • Phalacrocorax sp(p). (Late Miocene of Odesa region, Ukraine) – up to 4 species, one of which is probably P. longipes; Microcarbo, Phalacrocorax and/or Gulosus?[31]
  • Phalacrocorax femoralis (Modelo Late Miocene/Early Pliocene of WC North America) – formerly Miocorax; Nannopterum?
  • Phalacrocorax sp. (Late Miocene/Early Pliocene of Lee Creek Mine, US) – Nannopterum or Phalacrocorax?
  • Phalacrocorax sp. 1 (Late Miocene/Early Pliocene of WC South America) – probably Leucocarbo
  • Phalacrocorax sp. 2 (Pisco Late Miocene/Early Pliocene of SW Peru) – Poikilocarbo or Leucocarbo?
  • Phalacrocorax longipes (Late Miocene – Early Pliocene of Ukraine) – formerly Pliocarbo; Microcarbo, Phalacrocorax or Gulosus?
  • Phalacrocorax goletensis (Early Pliocene – Early Pleistocene of Mexico) – Urile or Nannopterum, perhaps Poikilocarbo or Leuocarbo
  • Phalacrocorax wetmorei (Bone Valley Early Pliocene of Florida) – Nannopterum or Phalacrocorax?
  • Phalacrocorax sp. (Bone Valley Early Pliocene of Polk County, Florida, US) – Nannopterum or Phalacrocorax?[32]
  • Phalacrocorax leptopus (Juntura Early/Middle Pliocene of Juntura, Malheur County, Oregon, US) – Nannopterum?
  • Phalacrocorax reliquus (Middle Pliocene of Mongolia) – Microcarbo, Phalacrocorax or Gulosus?
  • Phalacrocorax idahensis (Middle Pliocene – Pleistocene of Idaho, US, and possibly Florida) – Nannopterum?
  • Phalacrocorax destefanii (Late Pliocene of Italy) – formerly Paracorax; Microcarbo, Phalacrocorax or Gulosus?
  • Phalacrocorax filyawi (Pinecrest Late Pliocene of Florida, US) – may be P. idahensis; Nannopterum or Phalacrocorax, perhaps Urile?
  • Phalacrocorax kennelli (San Diego Late Pliocene of California, US) – Urile or Nannopterum?
  • Phalacrocorax kumeyaay (San Diego Late Pliocene of California, US) – Urile or Nannopterum?
  • Phalacrocorax macer (Late Pliocene of Idaho, US) – Nannopterum?
  • Phalacrocorax mongoliensis (Late Pliocene of W Mongolia) – Microcarbo, Phalacrocorax or Gulosus?
  • Phalacrocorax sp. (La Portada Late Pliocene of N Chile) – may be same as Late Miocene/Early Pliocene "Phalacrocorax sp. 2"; Poikilocarbo or Leucocarbo?
  • Phalacrocorax rogersi (Late Pliocene – Early Pleistocene of California, US) – Urile or Nannopterum?
  • Phalacrocorax chapalensis (Late Pliocene/Early Pleistocene of Jalisco, Mexico) – Urile or Nannopterum, perhaps Poikilocarbo or Leucocarbo?
  • Phalacrocorax gregorii (Late Pleistocene of Australia) – possibly not a valid species; Microcarbo, Phalacrocorax or Leucocarbo?
  • Phalacrocorax vetustus (Late Pleistocene of Australia) – formerly Australocorax, possibly not a valid species; Microcarbo, Phalacrocorax or Leucocarbo?
  • Phalacrocorax sp. (Sarasota County, Florida, US) – may be P. filawyi/idahensis; Nannopterum or Phalacrocorax?

The former "Phalacrocorax" (or "Oligocorax") mediterraneus is now considered to belong to the bathornithid Paracrax antiqua.[33] "P." subvolans was actually a darter (Anhinga).

In human culture

Cormorant fishing
Main article: Cormorant fishing
A Chinese fisherman with his two cormorants

Humans have used cormorants' fishing skills in various places in the world. Archaeological evidence suggests that cormorant fishing was practised in Ancient Egypt, Peru, Korea and India, but the strongest tradition has remained in China and Japan, where it reached commercial-scale level in some areas.[34] In Japan, cormorant fishing is called ukai (鵜飼). Traditional forms of ukai 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, Guangxi, cormorants are famous for fishing on the shallow Li River. In Gifu, the Japanese cormorant (P. capillatus) is used; Chinese fishermen often employ great cormorants (P. carbo).[35] In Europe, a similar practice was also used on Doiran Lake in the region of Macedonia.[36] James VI and I appointed a keeper of cormorants, John Wood, and built ponds at Westminster to train the birds to fish.[37]

In a common technique, 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, but is still practised as a cultural tradition.[35][34]

In folklore, literature, and art
Further information: Birds in culture
Cormorants catching Fish. Hanging silk scroll by Yūhi, Middle Edo period, Japan, 1755
Cormorant sculpture by Brian Fell on the Stone Jetty, Morecambe

Cormorants feature in heraldry and medieval ornamentation, usually in their "wing-drying" pose, which was seen as representing the Christian cross, and symbolizing nobility and sacrifice. For John Milton in Paradise Lost, the cormorant symbolizes greed: perched atop the Tree of Life, Satan took the form of a cormorant as he spied on Adam and Eve during his first intrusion into Eden.[38]

In some Scandinavian areas, they are considered good omen; in particular, in Norwegian tradition spirits of those lost at sea come to visit their loved ones disguised as cormorants.[38] For example, the Norwegian municipalities of Røst, Loppa and Skjervøy have cormorants in their coat of arms. The symbolic liver bird of Liverpool is commonly thought to be a cross between an eagle and a cormorant.

In Homer's epic poem The Odyssey, Odysseus (Ulysses) is saved by a compassionate sea nymph who takes the form of a cormorant.

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 baptised "Juana Maria" (her original name is lost). The woman had lived alone on the island for 18 years before being rescued. When removed from San Nicolas, she brought with her a green cormorant dress she made; this dress is reported to have been removed to the Vatican.

The bird has inspired numerous writers, including Amy Clampitt, who wrote a poem called "The Cormorant in its Element". The species she described may have been the pelagic cormorant, which is the only species in the temperate U.S. with the "slim head ... vermilion-strapped" and "big black feet" that she mentions.

A cormorant representing Blanche Ingram appears in the first of the fictional paintings by Jane in Charlotte Brontë's novel Jane Eyre.

In the Sherlock Holmes story "The Adventure of the Veiled Lodger", Dr. Watson warns that if there are further attempts to get at and destroy his private notes regarding his time with Holmes, "the whole story concerning the politician, the lighthouse, and the trained cormorant will be given to the public. There is at least one reader who will understand."

A cormorant is humorously mentioned as having had linseed oil rubbed into it by a wayward pupil during the "Growth and Learning" segment of the 1983 Monty Python movie Monty Python's The Meaning of Life.

The cormorant served as the hood ornament for the Packard automobile brand.[39]

Cormorants (and books about them written by a fictional ornithologist) are a recurring fascination of the protagonist in Jesse Ball's 2018 novel Census.

The Pokémon Cramorant, featured in the 8th generation of the video game series, closely resembles a cormorant in both design and name.

The cormorant was chosen as the emblem for the Ministry of Defence Joint Services Command and Staff College at Shrivenham. A bird famed for flight, sea fishing and land nesting was felt to be particularly appropriate for a college that unified leadership training and development for the Army, Navy and Royal Air Force.

After a member produced a mock magazine cover from a photograph of roosting cormorants, the bird became the unofficial mascot of the Pentax Discuss Mailing List with many posts dedicated to discussion of the photography of the species.[40]

See also

References
  1. Gill, Frank; Donsker, David; Rasmussen, Pamela, eds. (August 2022). "Storks, frigatebirds, boobies, darters, cormorants". IOU World Bird List Version 12.2. International Ornithologists' Union. Retrieved 21 November 2022.
  2. "Cormorants and shags". RSPB. Retrieved 27 July 2018.
  3. Elliott, KH; Ricklefs, RE; Gaston, AJ; Hatch, SA; Speakman, JR; Davoren, GK (2013). "High flight costs and low dive costs in auks support the biomechanical hypothesis for flightlessness in penguins". Proceedings of the National Academy of Sciences. 110 (23): 9380–9384. Bibcode:2013PNAS..110.9380E. doi:10.1073/pnas.1304838110. PMC 3677478. PMID 23690614.
  4. "Picture". nwdiveclub.com.
  5. "Birds diving beyond 50ft down and going horizontally there?!". NWDiveClub.com. Northwest Dive Club.
  6. Cormorants Deep Sea Dive Caught on Camera. Wildlife Conservation Society. 2011-12-14. Archived from the original on 2021-11-03.
  7. Gómez-Laich, Agustina; Yoda, Ken; Zavalaga, Carlos; Quintana, Flavio (14 September 2015). "Selfies of Imperial Cormorants (Phalacrocorax atriceps): What Is Happening Underwater?". PLOS ONE. 10 (9): e0136980. Bibcode:2015PLoSO..1036980G. doi:10.1371/journal.pone.0136980. ISSN 1932-6203. PMC 4569182. PMID 26367384.
  8. Cramp S, Simmons KEL (1977) Handbook of the Birds of the Western Palearctic Volume 1, Oxford University Press ISBN 0-19-857358-8
  9. Rijke AM (1968). "The water repellency and feather structure of cormorants, Phalacrocoracidae". J. Exp. Biol. 48: 185–189. doi:10.1242/jeb.48.1.185.
  10. Marchant S. M.; Higgins, P. J. (1990). Handbook of Australian, New Zealand and Antarctic Birds. Vol 1A. Oxford University Press.
  11. Hennemann, W. W., III (1984). "Spread-winged behaviour of double-crested and flightless cormorants Phalacrocorax auritus and P. harrisi: wing drying or thermoregulation?". Ibis. 126 (2): 230–239. doi:10.1111/j.1474-919X.1984.tb08002.x.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  12. Cook, Timothee R; Guillaume Leblanc (2007). "Why is wing-spreading behaviour absent in blue-eyed shags?" (PDF). Animal Behaviour. 74 (3): 649–652. doi:10.1016/j.anbehav.2006.11.024. S2CID 53201673.
  13. Curry-Lindahl, K (1970). "Spread-wing postures in Pelecaniformes and Ciconiiformes" (PDF). Auk. 87 (2): 371–372. doi:10.2307/4083936. JSTOR 4083936.
  14. Sellers, R. M. (1995). "Wing-spreading behavior of the cormorant Phalacrocorax carbo" (PDF). Ardea. 83: 27–36.
  15. Nelson, J. Bryan (2005). Pelicans, Cormorants and Their Relatives: Pelecanidae, Sulidae, Phalacrocoracidae, Anhingidae, Fregatidae, Phaethontidae. Oxford University Press. pp. 162–163. ISBN 0-19-857727-3.
  16. Bernstein, N. P; S J Maxson (1982). "Absence of Wing-spreading Behavior in the Antarctic Blue-eyed Shag (Phalacrocorax Atriceps Bransfieldensis)" (PDF). The Auk. 99 (3): 588–589.
  17. Jobling, James A. (2010). The Helm Dictionary of Scientific Bird Names. London: Christopher Helm. p. 301. ISBN 978-1-4081-2501-4.
  18. Kennedy et al. (2000), Mayr (2005)
  19. See Siegel-Causey (1988), Orta (1992) and Kennedy et al. (2000) for a review of classification schemes.
  20. Kennedy, M.; Spencer, H.G. (2014). "Classification of the cormorants of the world". Molecular Phylogenetics and Evolution. 79: 249–257. doi:10.1016/j.ympev.2014.06.020. PMID 24994028.
  21. Yarrell, William (1828). "On the xiphoid bone and its muscles in the Corvorant (Pelecanus carbo)". The Zoological Journal. 4: 234–237.
  22. Garrod, A. H. (2009). "1. Notes on the Anatomy of Plotus anhinga". Proceedings of the Zoological Society of London. 44: 335–345. doi:10.1111/j.1096-3642.1876.tb02572.x.
  23. Burger, A E (2015). "Functional Anatomy of the Feeding Apparatus of Four South African Cormorants". Zoologica Africana. 13: 81–102. doi:10.1080/00445096.1978.11447608.
  24. Shufeldt, R.W. (1915). "Comparative osteology of Harris's Flightless Cormorant (Nannopterum harrisi)". Emu. 15 (2): 86–114. doi:10.1071/MU915086.
  25. van Tets (1976), Siegel-Causey (1988)
  26. Kennedy et al. (2000)
  27. Kurochkin (1995)
  28. Hope (2002)
  29. Kuhl, Heiner; Frankl-Vilches, Carolina; Bakker, Antje; Mayr, Gerald; Nikolaus, Gerhard; Boerno, Stefan T; Klages, Sven; Timmermann, Bernd; Gahr, Manfred (2021-01-04). "An Unbiased Molecular Approach Using 3′-UTRs Resolves the Avian Family-Level Tree of Life". Molecular Biology and Evolution. 38 (1): 108–127. doi:10.1093/molbev/msaa191. ISSN 0737-4038. PMC 7783168. PMID 32781465.
  30. Hope (2002) and see Hesperornithes
  31. These are the fossils described in the same paper as Pelecanus odessanus and sometimes cited as "Phalacrocorax sp. Wildhalm", which is a widespread lapsus calami or printing error for the initial describer, Ignatiy Vidgal'm (Игнатий Видгальм in Russian, a German emigrant originally named Ignaz Wi(e)dhalm and often transcribed as "J. Widhalm"). He discussed three presumed species of cormorant under the provisional non-Linnean names "Haliaeus fossilis, var. Odessana major, medius, [a]nd minor" ("fossil cormorant, large/mid-sized/small Odessan variety"). While various different bones were assigned to the large species (and eventually referred to P. longipes), one small and one mid-sized tarsometatarsus fragment remained unassigned; a few proximal ends of the same bone were provisionally included in the large species, but exceed its more complete tarsometatarsi in size and may represent a distinct and even larger fourth species. The fossils are probably lost nowadays and even the original publication is held by very few libraries; this has so far prevented a thorough review of the remains, but one partial coracoid does not appear to belong to Phalacrocorax sensu stricto and may have been closer in habitus to North Pacific shags (Urile), but is unlikely to have been closely related to these: Howard (1932).
  32. A proximal ulna, Specimen PB 311, Pierce Brodkorb collection. Initially assigned to P. idahensis. However, it is far too large, being from a very big species possibly larger than a great cormorant: Murray (1970).
  33. Cracraft (1971)
  34. Richard J. King (1 October 2013). The Devil's Cormorant: A Natural History. University of New Hampshire Press. pp. 9–. ISBN 978-1-61168-225-0.
  35. "Cormorant Fishing "UKAI"". May 2001. Retrieved 23 June 2016.
  36. "About Dojran lake". Retrieved 23 June 2016.
  37. James Edmund Harting, The Ornithology of Shakespeare (London, 1871), p. 262: Frederick Devon, Issues of the Exchequer (London, 1836), pp. 333-5.
  38. Arin Murphy-Hiscock (18 January 2012). Birds - A Spiritual Field Guide: Explore the Symbology and Significance of These Divine Winged Messengers. Adams Media. pp. 48–49. ISBN 978-1-4405-2688-6.
  39. John Gunnell (January 2004). Standard Guide to 1950s American Cars. Krause Publications. p. 192. ISBN 0-87349-868-2.
  40. "cormorant". The Mail Archive. 22 December 2004. Retrieved 6 June 2023.

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