Seabird

This article is about marine birds. For other uses, see Seabird (disambiguation).

Seabirds (also known as marine birds) are birds that are adapted to life within the marine environment. While seabirds vary greatly in lifestyle, behaviour and physiology, they often exhibit striking convergent evolution, as the same environmental problems and feeding niches have resulted in similar adaptations. The first seabirds evolved in the Cretaceous period, and modern seabird families emerged in the Paleogene.

The sooty tern is highly aerial and marine and will spend months flying at sea, returning to land only for breeding.^[1]

In general, seabirds live longer, breed later and have fewer young than other birds do, but they invest a great deal of time in their young. Most species nest in colonies, which can vary in size from a few dozen birds to millions. Many species are famous for undertaking long annual migrations, crossing the equator or circumnavigating the Earth in some cases. They feed both at the ocean's surface and below it, and even feed on each other. Seabirds can be highly pelagic, coastal, or in some cases spend a part of the year away from the sea entirely.

Seabirds and humans have a long history together: they have provided food to hunters, guided fishermen to fishing stocks and led sailors to land. Many species are currently threatened by human activities, such as from oil spills, getting trapped in nets, and by climate change and severe weather. Conservation efforts include the establishment of wildlife refugees and adjustments to fishing techniques.

Classification

There exists no single definition of which groups, families and species are seabirds, and most definitions are in some way arbitrary. Elizabeth Shreiber and Joanne Burger, two seabird scientists, said, "The one common characteristic that all seabirds share is that they feed in saltwater; but, as seems to be true with any statement in biology, some do not."^[2] However, by convention all of the Sphenisciformes (penguins) and Procellariiformes (albatrosses and petrels), all of the Suliformes (gannets and cormorants) except the darters, and some of the Charadriiformes (the skuas, gulls, terns, auks and skimmers) are classified as seabirds. The phalaropes are usually included as well, since although they are waders ("shorebirds" in North America), two of the three species (Red and Red-necked) are oceanic for nine months of the year, crossing the equator to feed pelagically.^[3][4]

Loons and grebes, which nest on lakes but winter at sea, are usually categorized as water birds, not seabirds. Although there are a number of sea ducks in the family Anatidae that are truly marine in the winter, by convention they are usually excluded from the seabird grouping. Many waders (or shorebirds) and herons are also highly marine, living on the sea's edge (coast), but are also not treated as seabirds. Sea eagles and other fish-eating birds of prey are also typically excluded, however tied to marine environments they may be.^[5]

German paleontologist Gerald Mayr defined the "core waterbird" clade Aequornithes in 2010. This lineage gives rise to the Gaviiformes, Sphenisciformes, Procellariiformes, Ciconiiformes, Suliformes and Pelecaniformes.^[6] The tropicbirds are part of a lineage—Eurypygimorphae—that is a sister group to the Aequornithes.^[7]

Evolution and fossil record

Seabirds, by virtue of living in a geologically depositional environment (that is, in the sea where sediments are readily laid down), are well represented in the fossil record.^[2] They are first known to occur in the Cretaceous period, the earliest being the Hesperornithiformes, like Hesperornis regalis, a flightless loon-like seabird that could dive in a fashion similar to grebes and loons (using its feet to move underwater)^{[8][needs update]} but had a beak filled with sharp teeth.^[9] Flying Cretaceous seabirds do not exceed wingspans of two meters; any sizes were taken^{[clarification needed]} by piscivorous pterosaurs.^[10]

 

The Cretaceous seabird Hesperornis

While Hesperornis is not thought to have left descendants, the earliest modern seabirds also occurred in the Cretaceous, with a species called Tytthostonyx glauconiticus, which has features suggestive of Procellariiformes and Fregatidae.^[11] As a clade, the Aequornithes either became seabirds in a single transition in the Cretaceous or some lineages such as pelicans and frigatebirds adapted to sea living independently from freshwater-dwelling ancestors.^[12] In the Paleogene both pterosaurs and marine reptiles became extinct, allowing seabirds to expand ecologically. These post-extinction seas were dominated by early Procellariidae, giant penguins and two extinct families, the Pelagornithidae and the Plotopteridae (a group of large seabirds that looked like the penguins).^[13] Modern genera began their wide radiation in the Miocene, although the genus Puffinus (which includes today's Manx shearwater and sooty shearwater) might date back to the Oligocene.^[2] Within the Charadriiformes, the gulls and allies (Lari) became seabirds in the late Eocene, and then waders in the middle Miocene (Langhian).^[12] The highest diversity of seabirds apparently existed during the Late Miocene and the Pliocene. At the end of the latter, the oceanic food web had undergone a period of upheaval due to extinction of considerable numbers of marine species; subsequently, the spread of marine mammals seems to have prevented seabirds from reaching their erstwhile diversity.^{[14][needs update]}

Characteristics

Adaptations to life at sea

Seabirds have made numerous adaptations to living on and feeding in the sea. Wing morphology has been shaped by the niche an individual species or family has evolved, so that looking at a wing's shape and loading can tell a scientist about its life feeding behaviour. Longer wings and low wing loading are typical of more pelagic species, while diving species have shorter wings.^[15] Species such as the wandering albatross, which forage over huge areas of sea, have a reduced capacity for powered flight and are dependent on a type of gliding called dynamic soaring (where the wind deflected by waves provides lift) as well as slope soaring.^[16] Seabirds also almost always have webbed feet, to aid movement on the surface as well as assisting diving in some species. The Procellariiformes are unusual among birds in having a strong sense of smell, which is used to find widely distributed food in a vast ocean,^[17] and help distinguish familiar nest odours from unfamiliar ones.^[18]

 

Cormorants, like this double-crested cormorant, have plumage that is partly wettable. This functional adaptation balances the competing requirement for thermoregulation against that of the need to reduce buoyancy.^[19]

Salt glands are used by seabirds to deal with the salt they ingest by drinking and feeding (particularly on crustaceans), and to help them osmoregulate.^[20] The excretions from these glands (which are positioned in the head of the birds, emerging from the nasal cavity) are almost pure sodium chloride.^[21]

With the exception of the cormorants and some terns, and in common with most other birds, all seabirds have waterproof plumage. However, compared to land birds, they have far more feathers protecting their bodies. This dense plumage is better able to protect the bird from getting wet, and cold is kept out by a dense layer of down feathers. The cormorants possess a layer of unique feathers that retain a smaller layer of air (compared to other diving birds) but otherwise soak up water.^[19] This allows them to swim without fighting the buoyancy that retaining air in the feathers causes, yet retain enough air to prevent the bird losing excessive heat through contact with water.^[22]

The plumage of most seabirds is less colourful than that of land birds, restricted in the main to variations of black, white or grey.^[15] A few species sport colourful plumes (such as the tropicbirds and some penguins), but most of the colour in seabirds appears in the bills and legs. The plumage of seabirds is thought in many cases to be for camouflage, both defensive (the colour of US Navy battleships is the same as that of Antarctic prions,^[15] and in both cases it reduces visibility at sea) and aggressive (the white underside possessed by many seabirds helps hide them from prey below). The usually black wing tips help prevent wear, as they contain melanins to make them black that helps the feathers resist abrasion.^[23]

Diet and feeding

Seabirds evolved to exploit different food resources in the world's seas and oceans, and to a great extent, their physiology and behaviour have been shaped by their diet. These evolutionary forces have often caused species in different families and even orders to evolve similar strategies and adaptations to the same problems, leading to remarkable convergent evolution, such as that between auks and penguins. There are four basic feeding strategies, or ecological guilds, for feeding at sea: surface feeding, pursuit diving, plunge-diving, and predation of higher vertebrates; within these guilds, there are multiple variations on the theme.^[24]

Surface feeding

Many seabirds feed on the ocean's surface, as the action of marine currents often concentrates food such as krill, forage fish, squid, or other prey items within reach of a dipped head.

 

Wilson's storm petrels pattering on the water's surface

Surface feeding itself can be broken up into two different approaches, surface feeding while flying (for example as practiced by gadfly petrels, frigatebirds, and storm petrels), and surface feeding while swimming (examples of which are practiced by fulmars, gulls, many of the shearwaters and gadfly petrels). Surface feeders in flight include some of the most acrobatic of seabirds, which either snatch morsels from the water (as do frigate-birds and some terns), or "walk", pattering and hovering on the water's surface, as some of the storm-petrels do.^[25] Many of these do not ever land in the water, and some, such as the frigatebirds, have difficulty getting airborne again should they do so.^[26] Another seabird family that does not land while feeding is the skimmer, which has a unique fishing method: flying along the surface with the lower mandible in the water—this shuts automatically when the bill touches something in the water. The skimmer's bill reflects its unusual lifestyle, with the lower mandible uniquely being longer than the upper one.^[27]

Surface feeders that swim often have unique bills as well, adapted for their specific prey. Prions have special bills with filters called lamellae to filter out plankton from mouthfuls of water,^[28] and many albatrosses and petrels have hooked bills to snatch fast-moving prey. On the other hand, most gulls are versatile and opportunistic feeders who will eat a wide variety of prey, both at sea and on land.^[29]

Pursuit diving

 

An African penguin skeleton, showing the sternal keel that makes the species a strong diver and swimmer

Pursuit diving exerts greater pressures (both evolutionary and physiological) on seabirds, but the reward is a greater area in which to feed than is available to surface feeders. Underwater propulsion is provided by wings (as used by penguins, auks, diving petrels and some other species of petrel) or feet (as used by cormorants, grebes, loons and several types of fish-eating ducks). Wing-propelled divers are generally faster than foot-propelled divers.^[2] The use of wings or feet for diving has limited their utility in other situations: loons and grebes walk with extreme difficulty (if at all), penguins cannot fly, and auks have sacrificed flight efficiency in favour of diving. For example, the razorbill (an Atlantic auk) requires 64% more energy to fly than a petrel of equivalent size.^[30] Many shearwaters are intermediate between the two, having longer wings than typical wing-propelled divers but heavier wing loadings than the other surface-feeding procellariids, leaving them capable of diving to considerable depths while still being efficient long-distance travellers. The short-tailed shearwater is the deepest diver of the shearwaters, having been recorded diving below 70 metres (230 ft).^[31]

Some albatross species are also capable of limited diving, with light-mantled sooty albatrosses holding the record at 12 metres (40 ft).^[32] Of all the wing-propelled pursuit divers, the most efficient in the air are the albatrosses, and they are also the poorest divers. This is the dominant guild in polar and subpolar environments, but it is energetically inefficient in warmer waters. With their poor flying ability, many wing-propelled pursuit divers are more limited in their foraging range than other guilds.^[33]

Plunge diving

Gannets, boobies, tropicbirds, some terns, and brown pelicans all engage in plunge diving, taking fast-moving prey by diving into the water from the flight. Plunge diving allows birds to use the energy from the momentum of the dive to combat natural buoyancy (caused by air trapped in plumage),^[34] and thus uses less energy than the dedicated pursuit divers, allowing them to utilise more widely distributed food resources, for example, in impoverished tropical seas. In general, this is the most specialised method of hunting employed by seabirds; other non-specialists (such as gulls and skuas) may employ it but do so with less skill and from lower heights. In brown pelicans the skills of plunge-diving take several years to fully develop—once mature, they can dive from 20 m (70 ft) above the water's surface, shifting the body before impact to avoid injury.^[35]

It may be that plunge divers are restricted in their hunting grounds to clear waters that afford a view of their prey from the air.^[36] While they are the dominant guild in the tropics, the link between plunge diving and water clarity is inconclusive.^[37] Some plunge divers (as well as some surface feeders) are dependent on dolphins and tuna to push shoaling fish up towards the surface.^[38]

Kleptoparasitism, scavenging and predation

This catch-all category refers to other seabird strategies that involve the next trophic level up. Kleptoparasites are seabirds that make a part of their living stealing food of other seabirds. Most famously, frigatebirds and skuas engage in this behaviour, although gulls, terns and other species will steal food opportunistically.^[39] The nocturnal nesting behaviour of some seabirds has been interpreted as arising due to pressure from this aerial piracy.^[40] Kleptoparasitism is not thought to play a significant part of the diet of any species, and is instead a supplement to food obtained by hunting.^[2] A study of great frigatebirds stealing from masked boobies estimated that the frigatebirds could at most obtain 40% of the food they needed, and on average obtained only 5%.^[41] Many species of gull will feed on seabird and sea mammal carrion when the opportunity arises, as will giant petrels. Some species of albatross also engage in scavenging: an analysis of regurgitated squid beaks has shown that many of the squid eaten are too large to have been caught alive, and include mid-water species likely to be beyond the reach of albatrosses.^[42] Some species will also feed on other seabirds; for example, gulls, skuas and pelicans will often take eggs, chicks and even small adult seabirds from nesting colonies, while the giant petrels can kill prey up to the size of small penguins and seal pups.^[43]

Life history

Seabirds' life histories are dramatically different from those of land birds. In general, they are K-selected, live much longer (anywhere between twenty and sixty years), delay breeding for longer (for up to ten years), and invest more effort into fewer young.^[2][44] Most species will only have one clutch a year, unless they lose the first (with a few exceptions, like the Cassin's auklet),^[45] and many species (like the tubenoses and sulids) will only lay one egg a year.^[28]

 

Northern gannet pair "billing" during courtship; like all seabirds except the phalaropes they maintain a pair bond throughout the breeding season.

Care of young is protracted, extending for as long as six months, among the longest for birds. For example, once common guillemot chicks fledge, they remain with the male parent for several months at sea.^[30] The frigatebirds have the longest period of parental care of any bird except a few raptors and the southern ground hornbill,^[46] with each chick fledging after four to six months and continued assistance after that for up to fourteen months.^[47] Due to the extended period of care, breeding occurs every two years rather than annually for some species. This life-history strategy has probably evolved both in response to the challenges of living at sea (collecting widely scattered prey items), the frequency of breeding failures due to unfavourable marine conditions, and the relative lack of predation compared to that of land-living birds.^[2]

Because of the greater investment in raising the young and because foraging for food may occur far from the nest site, in all seabird species except the phalaropes, both parents participate in caring for the young, and pairs are typically at least seasonally monogamous. Many species, such as gulls, auks and penguins, retain the same mate for several seasons, and many petrel species mate for life.^[28] Albatrosses and procellariids, which mate for life, take many years to form a pair bond before they breed, and the albatrosses have an elaborate breeding dance that is part of pair-bond formation.^[48]

Breeding and colonies

See also: Bird colony and Seabird breeding behavior

 

Common murres breed on densely packed colonies on offshore rocks, islands and cliffs.

Ninety-five percent of seabirds are colonial,^[2] and seabird colonies are among the largest bird colonies in the world, providing one of Earth's great wildlife spectacles. Colonies of over a million birds have been recorded, both in the tropics (such as Kiritimati in the Pacific) and in the polar latitudes (as in Antarctica). Seabird colonies occur exclusively for the purpose of breeding; non-breeding birds will only collect together outside the breeding season in areas where prey species are densely aggregated.^{[citation needed]}

Seabird colonies are highly variable. Individual nesting sites can be widely spaced, as in an albatross colony, or densely packed as with a murre colony. In most seabird colonies, several different species will nest on the same colony, often exhibiting some niche separation. Seabirds can nest in trees (if any are available), on the ground (with or without nests), on cliffs, in burrows under the ground and in rocky crevices. Competition can be strong both within species and between species, with aggressive species such as sooty terns pushing less dominant species out of the most desirable nesting spaces.^[49] The tropical Bonin petrel nests during the winter to avoid competition with the more aggressive wedge-tailed shearwater. When the seasons overlap, the wedge-tailed shearwaters will kill young Bonin petrels in order to use their burrows.^[50]

Many seabirds show remarkable site fidelity, returning to the same burrow, nest or site for many years, and they will defend that site from rivals with great vigour.^[2] This increases breeding success, provides a place for returning mates to reunite, and reduces the costs of prospecting for a new site.^[51] Young adults breeding for the first time usually return to their natal colony, and often nest close to where they hatched. This tendency, known as philopatry, is so strong that a study of Laysan albatrosses found that the average distance between hatching site and the site where a bird established its own territory was 22 metres (72 ft);^[52] another study, this time on Cory's shearwaters nesting near Corsica, found that of nine out of 61 male chicks that returned to breed at their natal colony bred in the burrow they were raised in, and two actually bred with their own mother.^[53]

Colonies are usually situated on islands, cliffs or headlands, which land mammals have difficulty accessing.^[54] This is thought to provide protection to seabirds, which are often very clumsy on land. Coloniality often arises in types of bird that do not defend feeding territories (such as swifts, which have a very variable prey source); this may be a reason why it arises more frequently in seabirds.^[2] There are other possible advantages: colonies may act as information centres, where seabirds returning to the sea to forage can find out where prey is by studying returning individuals of the same species. There are disadvantages to colonial life, particularly the spread of disease. Colonies also attract the attention of predators, principally other birds, and many species attend their colonies nocturnally to avoid predation.^[55] Birds from different colonies often forage in different areas to avoid competition.^[56]

Migration

 

Pelican flock flying over Havana Bay area. These birds come to Cuba every year from North America in the northern hemisphere winter season.

 

Arctic terns breed in the arctic and subarctic and winter in Antarctica.

Like many birds, seabirds often migrate after the breeding season. Of these, the trip taken by the Arctic tern is the farthest of any bird, crossing the equator in order to spend the Austral summer in Antarctica. Other species also undertake trans-equatorial trips, both from the north to the south, and from south to north. The population of elegant terns, which nest off Baja California, splits after the breeding season with some birds travelling north to the Central Coast of California and some travelling as far south as Peru and Chile to feed in the Humboldt Current.^[57] The sooty shearwater undertakes an annual migration cycle that rivals that of the Arctic tern; birds that nest in New Zealand and Chile and spend the northern summer feeding in the North Pacific off Japan, Alaska and California, an annual round trip of 64,000 kilometres (40,000 mi).^[58]

Other species also migrate shorter distances away from the breeding sites, their distribution at sea determined by the availability of food. If oceanic conditions are unsuitable, seabirds will emigrate to more productive areas, sometimes permanently if the bird is young.^[59] After fledging, juvenile birds often disperse further than adults, and to different areas, so are commonly sighted far from a species' normal range. Some species, such as the auks, do not have a concerted migration effort, but drift southwards as the winter approaches.^[30] Other species, such as some of the storm petrels, diving petrels and cormorants, never disperse at all, staying near their breeding colonies year round.^[60][61][62]

Away from the sea

While the definition of seabirds suggests that the birds in question spend their lives on the ocean, many seabird families have many species that spend some or even most of their lives inland away from the sea. Most strikingly, many species breed tens, hundreds or even thousands of miles inland. Some of these species still return to the ocean to feed; for example, the snow petrel, the nests of which have been found 480 kilometres (300 mi) inland on the Antarctic mainland, are unlikely to find anything to eat around their breeding sites.^[63] The marbled murrelet nests inland in old growth forest, seeking huge conifers with large branches to nest on.^[64] Other species, such as the California gull, nest and feed inland on lakes, and then move to the coasts in the winter.^[65] Some cormorant, pelican, gull and tern species have individuals that never visit the sea at all, spending their lives on lakes, rivers, swamps and, in the case of some of the gulls, cities and agricultural land. In these cases it is thought that these terrestrial or freshwater birds evolved from marine ancestors.^[15] Some seabirds, principally those that nest in tundra, as skuas and phalaropes do, will migrate over land as well.^[3][66]

The more marine species, such as petrels, auks and gannets, are more restricted in their habits, but are occasionally seen inland as vagrants. This most commonly happens to young inexperienced birds, but can happen in great numbers to exhausted adults after large storms, an event known as a wreck.^[67]

Relationship with humans

Seabirds and fisheries

Seabirds have had a long association with both fisheries and sailors, and both have drawn benefits and disadvantages from the relationship.

Fishermen have traditionally used seabirds as indicators of both fish shoals,^[38] underwater banks that might indicate fish stocks, and of potential landfall. In fact, the known association of seabirds with land was instrumental in allowing the Polynesians to locate tiny landmasses in the Pacific.^[2] Seabirds have provided food for fishermen away from home, as well as bait. Famously, tethered cormorants have been used to catch fish directly. Indirectly, fisheries have also benefited from guano from colonies of seabirds acting as fertilizer for the surrounding seas.^[68]

Negative effects on fisheries are mostly restricted to raiding by birds on aquaculture,^[69] although long-lining fisheries also have to deal with bait stealing. There have been claims of prey depletion by seabirds of fishery stocks, and while there is some evidence of this, the effects of seabirds are considered smaller than that of marine mammals and predatory fish (like tuna).^[2]

 

Seabirds (mostly northern fulmars) flocking at a long-lining vessel

Some seabird species have benefited from fisheries, particularly from discarded fish and offal. These discards compose 30% of the food of seabirds in the North Sea, for example, and compose up to 70% of the total food of some seabird populations.^[70] This can have other impacts; for example, the spread of the northern fulmar through the United Kingdom is attributed in part to the availability of discards.^[71] Discards generally benefit surface feeders, such as gannets and petrels, to the detriment of pursuit divers like penguins and guillemots, which can get entangled in the nets.^[72]

Fisheries also have negative effects on seabirds, and these effects, particularly on the long-lived and slow-breeding albatrosses, are a source of increasing concern to conservationists. The bycatch of seabirds entangled in nets or hooked on fishing lines has had a big impact on seabird numbers; for example, an estimated 100,000 albatrosses are hooked and drown each year on tuna lines set out by long-line fisheries.^{[73][74][needs update]} Overall, many hundreds of thousands of birds are trapped and killed each year, a source of concern for some of the rarest species (for example, only about 2,000 short-tailed albatrosses are known to still exist). Seabirds are also thought to suffer when overfishing occurs.^[75] Changes to the marine ecosystems caused by dredging, which alters the biodiversity of the seafloor, can also have a negative impact.^[76]

Exploitation

The hunting of seabirds and the collecting of seabird eggs have contributed to the declines of many species, and the extinction of several, including the great auk and the spectacled cormorant. Seabirds have been hunted for food by coastal peoples throughout history—one of the earliest instances known is in southern Chile, where archaeological excavations in middens has shown hunting of albatrosses, cormorants and shearwaters from 5000 BP.^[77] This pressure has led to some species becoming extinct in many places; in particular, at least 20 species of an original 29 no longer breed on Easter Island. In the 19th century, the hunting of seabirds for fat deposits and feathers for the millinery trade reached industrial levels. Muttonbirding (harvesting shearwater chicks) developed as important industries in both New Zealand and Tasmania, and the name of one species, the providence petrel, is derived from its seemingly miraculous arrival on Norfolk Island where it provided a windfall for starving European settlers.^[78] In the Falkland Islands, hundreds of thousands of penguins were harvested for their oil each year. Seabird eggs have also long been an important source of food for sailors undertaking long sea voyages, as well as being taken when settlements grow in areas near a colony. Eggers from San Francisco took almost half a million eggs a year from the Farallon Islands in the mid-19th century, a period in the islands' history from which the seabird species are still recovering.^[79]

Both hunting and egging continue today, although not at the levels that occurred in the past, and generally in a more controlled manner. For example, the Māori of Stewart Island/Rakiura continue to harvest the chicks of the sooty shearwater as they have done for centuries, using traditional stewardship, kaitiakitanga, to manage the harvest, but now also work with the University of Otago in studying the populations.^[80] In Greenland, however, uncontrolled hunting is pushing many species into steep decline.^[81]

Other threats

See also: Introduced mammals on seabird breeding islands

 

This crested auklet was oiled in Alaska during the spill of MV Selendang Ayu in 2004.

Other human factors have led to declines and even extinctions in seabird populations and species. Of these, perhaps the most serious are introduced species. Seabirds, breeding predominantly on small isolated islands, are vulnerable to predators because they have lost many behaviours associated with defence from predators.^[54] Feral cats can take seabirds as large as albatrosses, and many introduced rodents, such as the Pacific rat, take eggs hidden in burrows. Introduced goats, cattle, rabbits and other herbivores can create problems, particularly when species need vegetation to protect or shade their young.^[82] The disturbance of breeding colonies by humans is often a problem as well—visitors, even well-meaning tourists, can flush brooding adults off a colony, leaving chicks and eggs vulnerable to predators.^[83][84]

The build-up of toxins and pollutants in seabirds is also a concern. Seabirds, being apex predators, suffered from the ravages of the insecticide DDT until it was banned; DDT was implicated, for example, in embryo development problems and the skewed sex ratio of western gulls in southern California.^[85] Oil spills are also a threat to seabirds: the oil is toxic, and bird feathers become saturated by the oil, causing them to lose their waterproofing.^[86] Oil pollution in particular threatens species with restricted ranges or already depressed populations.^[87][88]

Climate change mainly affect seabirds via changes to their habitat: various processes in the ocean lead to decreased availability of food and colonies are more often flooded as a consequence of sea level rise and extreme rainfall events. Heat stress from extreme temperatures is an additional threat.^[89] Some seabirds have used changing wind patterns to forage further and more efficiently.^[90]

Conservation

The threats faced by seabirds have not gone unnoticed by scientists or the conservation movement. As early as 1903, U.S. President Theodore Roosevelt was convinced of the need to declare Pelican Island in Florida a National Wildlife Refuge to protect the bird colonies (including the nesting brown pelicans),^[91] and in 1909 he protected the Farallon Islands. Today many important seabird colonies are given some measure of protection, from Heron Island in Australia to Triangle Island in British Columbia.^[92][93]

Island restoration techniques, pioneered by New Zealand, enable the removal of exotic invaders from increasingly large islands. Feral cats have been removed from Ascension Island, Arctic foxes from many islands in the Aleutian Islands,^[94] and rats from Campbell Island. The removal of these introduced species has led to increases in numbers of species under pressure and even the return of extirpated ones. After the removal of cats from Ascension Island, seabirds began to nest there again for the first time in over a hundred years.^[95]

Seabird mortality caused by long-line fisheries can be greatly reduced by techniques such as setting long-line bait at night, dying the bait blue, setting the bait underwater, increasing the amount of weight on lines and by using bird scarers,^[96] and their deployment is increasingly required by many national fishing fleets.

One of the Millennium Projects in the UK was the Scottish Seabird Centre, near the important bird sanctuaries on Bass Rock, Fidra and the surrounding islands. The area is home to huge colonies of gannets, puffins, skuas and other seabirds. The centre allows visitors to watch live video from the islands as well as learn about the threats the birds face and how we can protect them, and has helped to significantly raise the profile of seabird conservation in the UK. Seabird tourism can provide income for coastal communities as well as raise the profile of seabird conservation, although it needs to be managed to ensure it does not harm the colonies and nesting birds.^[97] For example, the northern royal albatross colony at Taiaroa Head in New Zealand attracts 40,000 visitors a year.^[28]

The plight of albatross and large seabirds, as well as other marine creatures, being taken as bycatch by long-line fisheries, has been addressed by a large number of non-governmental organizations (including BirdLife International, the American Bird Conservancy and the Royal Society for the Protection of Birds).^{[98][99][100]} This led to the Agreement on the Conservation of Albatrosses and Petrels, a legally binding treaty designed to protect these threatened species, which has been ratified by thirteen countries as of 2021 (Argentina, Australia, Brazil, Chile, Ecuador, France, New Zealand, Norway, Peru, South Africa, Spain, Uruguay, United Kingdom).^[101]

Role in culture

 

Depiction of a pelican with chicks on a stained glass window, Saint Mark's Church, Gillingham, Kent

Many seabirds are little studied and poorly known because they live far out at sea and breed in isolated colonies. Some seabirds, particularly the albatrosses and gulls, are more well known to humans. The albatross has been described as "the most legendary of birds",^[102] and have a variety of myths and legends associated with them. While it is widely considered unlucky to harm them, the notion that sailors believed that is a myth^[103] that derives from Samuel Taylor Coleridge's famous poem, "The Rime of the Ancient Mariner", in which a sailor is punished for killing an albatross by having to wear its corpse around his neck. Sailors did, however, consider it unlucky to touch a storm petrel, especially one that landed on the ship.^[104]

Gulls are one of the most commonly seen seabirds because they frequent human-made habitats (such as cities and dumps) and often show a fearless nature. Gulls have been used as metaphors, as in Jonathan Livingston Seagull by Richard Bach, or to denote a closeness to the sea; in The Lord of the Rings, they appear in the insignia of Gondor and therefore Númenor (used in the design of the films), and they call Legolas to (and across) the sea. Pelicans have long been associated with mercy and altruism because of an early Christian myth that they split open their breast to feed their starving chicks.^[35]

Seabird families

The following are the groups of birds normally classed as seabirds.^{[citation needed]}

Sphenisciformes (Antarctic and southern waters; 16 species)

• Spheniscidae penguins

Procellariiformes (Tubenoses: pan-oceanic and pelagic; 93 species)

• Diomedeidae albatrosses
• Procellariidae fulmars, prions, shearwaters, gadfly and other petrels
• Pelacanoididae diving petrels
• Hydrobatidae storm petrels

Pelecaniformes (Worldwide; 8 species)

• Pelecanidae pelicans

Suliformes (Worldwide; about 56 species)

• Sulidae gannets and boobies
• Phalacrocoracidae cormorants
• Fregatidae frigatebirds

Phaethontiformes (Worldwide tropical seas; 3 species)

• Phaethontidae tropicbirds

Charadriiformes (Worldwide; 305 species, but only the families listed are classed as seabirds.)

• Stercorariidae skuas
• Laridae gulls
• Sternidae terns
• Rhynchopidae skimmers
• Alcidae auks

For an alternative taxonomy of these groups, see also Sibley-Ahlquist taxonomy.

References

1. BirdLife International (2020). "Onychoprion fuscatus". IUCN Red List of Threatened Species. 2020: e.T22694740A168895142. doi:10.2305/IUCN.UK.2020-3.RLTS.T22694740A168895142.en. Retrieved November 12, 2021.
2. Schreiber, Elizabeth A. and Burger, Joanne (2001) Biology of Marine Birds. Boca Raton: CRC Press, ISBN 0-8493-9882-7
3. Rubega, Margaret A.; Schamel, Douglas; Tracy, Diane M. (March 4, 2020). "Red-necked Phalarope (Phalaropus lobatus), version 1.0". Birds of the World. Cornell Lab of Ornithology. doi:10.2173/bow.renpha.01. S2CID 216464615. Retrieved March 26, 2021.
4. Tracy, Diane M.; Schamel, Douglas; Dale, James (March 4, 2020). "Red Phalarope (Phalaropus fulicarius), version 1.0". Birds of the World. Cornell Lab of Ornithology. doi:10.2173/bow.redpha1.01. S2CID 216176285. Retrieved March 26, 2021.
5. Brooke, Michael (2018). Far From Land: The Mysterious Lives of Seabirds. Princeton: Princeton University Press. pp. 5–11. ISBN 978-0-691-17418-1.
6. Burleigh, J.G.; et al. (March 2015). "Building the avian tree of life using a large-scale, sparse supermatrix". Molecular Phylogenetics and Evolution. 84: 53–63. doi:10.1016/j.ympev.2014.12.003. PMID 25550149.
7. Jarvis, E.D.; et al. (2014). "Whole-genome analyses resolve early branches in the tree of life of modern birds". Science. 346 (6215): 1320–1331. Bibcode:2014Sci...346.1320J. doi:10.1126/science.1253451. PMC 4405904. PMID 25504713.
8. Johansson, L. C.; Lindhe Norberg, U. M. (2001). "Lift-based paddling in diving grebe". Journal of Experimental Biology. 204 (10): 1687–1696. doi:10.1242/jeb.204.10.1687. PMID 11316488.
9. Gregory, Joseph T. (1952). "The jaws of the Cretaceous toothed birds, Ichthyornis and Hesperornis" (PDF). Condor. 54 (2): 73–88. doi:10.2307/1364594. JSTOR 1364594.
10. Longrich, N. R.; Martill, D. M.; Andres, B. (2018). "Late Maastrichtian pterosaurs from North Africa and mass extinction of Pterosauria at the Cretaceous-Paleogene boundary". PLOS Biology. 16 (3): e2001663. doi:10.1371/journal.pbio.2001663. PMC 5849296. PMID 29534059.
11. Olson, S.; Parris, D.C. (1987). "The Cretaceous Birds of New Jersey." Smithsonian Contributions to Paleontology, 63: 22pp.
12. Vermeij, Geerat; Motani, Ryosuke (2018). "Land to sea transitions in vertebrates: The dynamics of colonization". Paleobiology. 44 (2): 237–250. doi:10.1017/pab.2017.37. S2CID 91116726.
13. Goedert, James L. (1989). "Giant late Eocene marine birds (Pelecaniformes: Pelagornithidae) from northwestern Oregon". Journal of Paleontology. 63 (6): 939–944. doi:10.1017/S0022336000036647. JSTOR 1305659. S2CID 132978790.
14. Olson, S.; Hasegawa, Y. (1979). "Fossil counterparts of giant penguins from the north Pacific". Science. 206 (4419): 688–689. Bibcode:1979Sci...206..688O. doi:10.1126/science.206.4419.688. PMID 17796934. S2CID 12404154.
15. Gaston, Anthony J. (2004). Seabirds: A Natural History New Haven:Yale University Press, ISBN 0-300-10406-5
16. Pennycuick, C. J. (1982). "The flight of petrels and albatrosses (Procellariiformes), observed in South Georgia and its vicinity". Philosophical Transactions of the Royal Society B. 300 (1098): 75–106. Bibcode:1982RSPTB.300...75P. doi:10.1098/rstb.1982.0158.
17. Lequette, B.; Verheyden, C.; Jowentin, P. (1989). "Olfaction in Subantarctic seabirds: Its phylogenetic and ecological significance" (PDF). The Condor. 91 (3): 732–735. doi:10.2307/1368131. JSTOR 1368131.
18. Mitkus, Mindaugas; Nevitt, Gabrielle A.; Kelber, Almut (2018). "Development of the Visual System in a Burrow-Nesting Seabird: Leach's Storm Petrel". Brain, Behavior and Evolution. 91 (1): 4–16. doi:10.1159/000484080. ISSN 0006-8977. PMID 29212065. S2CID 4964467. Retrieved March 15, 2021 – via Karger.
19. Grémillet, D.; Chauvin, C.; Wilson, R. P.; Le Maho, Y.; Wanless, S. (2005). "Unusual feather structure allows partial plumage wettability in diving great cormorants Phalacrocorax carbo". Journal of Avian Biology. 36 (1): 57–63. doi:10.1111/j.0908-8857.2005.03331.x.
20. Harrison, C. S. (1990) Seabirds of Hawaii, Natural History and Conservation Ithaca:Cornell University Press, ISBN 0-8014-2449-6
21. Schmidt-Nielson, Knut (May 1960). "The Salt-Secreting Gland of Marine Birds". Circulation. 21 (5): 955–967. doi:10.1161/01.CIR.21.5.955. PMID 14443123.
22. King, Richard J. (2013). The Devil's Cormorant: A Natural History. Durham, NH: University of New Hampshire Press. p. 233. ISBN 978-1-61168-699-9.
23. Elphick, Jonathan (2016). Birds: A Complete Guide to their Biology and Behavior. Buffalo, New York: Firefly Books. p. 80. ISBN 978-1-77085-762-9.
24. Castro, Peter; Huber, Michael E. (2003). Marine Biology. University of Michigan: McGraw-Hill. p. 186. ISBN 0070294216.
25. Withers, P. C. (1979). "Aerodynamics and hydrodynamics of the 'hovering' flight of Wilson's storm petrel". Journal of Experimental Biology. 80: 83–91. doi:10.1242/jeb.80.1.83.
26. Metz, V. G. and Schreiber, E. A. (2002). Great Frigatebird (Fregata minor). In The Birds of North America, No. 681 (A. Poole and F. Gill, eds.). The Birds of North America, Inc., Philadelphia, PA
27. Zusi, R. L. (1996), "Family Rynchopidae (Skimmers)", in del Hoyo, Josep; Elliott, Andrew; Sargatal, Jordi (eds.), Handbook of the Birds of the World. Volume 3, Hoatzin to Auks, Barcelona: Lynx Edicions, pp. 668–675, ISBN 84-87334-20-2
28. Brooke, M. (2004). Albatrosses and Petrels Across the World. Oxford University Press, Oxford, UK ISBN 0-19-850125-0
29. Davenport, John; D. Black, Kenn; Burnell, Gavin; Cross, Tom; Culloty, Sarah; Ekaratne, Suki; Furness, Bob; Mulcahy, Maire; Thetmeyer, Helmut (2009). Aquaculture: The Ecological Issues. John Wiley & Sons. p. 68. ISBN 978-1444311259.
30. Gaston, Anthony J.; Jones, Ian L. (1998). The Auks, Oxford University Press, Oxford, ISBN 0-19-854032-9
31. Weimerskirch, H.; Cherel, Y. (1998). "Feeding ecology of short-tailed shearwaters: breeding in Tasmania and foraging in the Antarctic?". Marine Ecology Progress Series. 167: 261–274. Bibcode:1998MEPS..167..261W. doi:10.3354/meps167261.
32. Prince, P. A.; Huin, N.; Weimerskirch, H. (1994). "Diving depths of albatrosses". Antarctic Science. 6 (3): 353–354. Bibcode:1994AntSc...6..353P. doi:10.1017/S0954102094000532. S2CID 129728675.
33. Ulanski, Stan (2016). The California Current: A Pacific Ecosystem and Its Fliers, Divers, and Swimmers. UNC Press Books. p. 99. ISBN 978-0070294219.
34. Ropert-Coudert, Y.; Grémillet, D.; Ryan, P.; Kato, A.; Naito, Y.; Le Maho, Y. (2004). "Between air and water: the plunge dive of the Cape Gannet Morus capensis". Ibis. 146 (2): 281–290. doi:10.1111/j.1474-919x.2003.00250.x.
35. Elliot, A. (1992). "Family Pelecanidae (Pelicans)". In del Hoyo, J.; Elliott, A.; Sargatal, J. (eds.). Handbook of the Birds of the World. Vol. 1: Ostrich to Ducks. Barcelona, Spain: Lynx Edicions. pp. 290–311. ISBN 84-87334-10-5.
36. Ainley, D. G. (1977) "Feeding methods in seabirds: a comparison of polar and tropical nesting communities in the eastern Pacific Ocean". In: Llano, G. A. (Ed.). Adaptations within Antarctic ecosystems. Smithsonian Inst. Washington D.C., pp. 669–685
37. Haney, J. C. & Stone, A. E. (1988). "Seabird foraging tactics and water clarity: Are plunge divers really in the clear?". Marine Ecology Progress Series. 49: 1–9. Bibcode:1988MEPS...49....1H. doi:10.3354/meps049001.
38. Au, D. W. K. & Pitman, R. L. (1986). "Seabird interactions with Dolphins and Tuna in the Eastern Tropical Pacific" (PDF). Condor. 88 (3): 304–317. doi:10.2307/1368877. JSTOR 1368877.
39. Schnell, G.; Woods, B.; Ploger B. (1983). "Brown Pelican foraging success and kleptoparasitism by Laughing Gulls". Auk. 100 (3): 636–644. doi:10.1093/auk/100.3.636.
40. Gaston, A. J.; Dechesne, S. B. C. (1996). Rhinoceros Auklet (Cerorhinca monocerata). In The Birds of North America, No. 212 (A. Poole and F. Gill, eds.). The Academy of Natural Sciences, Philadelphia, PA, and The American Ornithologists' Union, Washington, D.C
41. Vickery, J.; Brooke, M. (1994). "The kleptoparasitic interactions between Great Frigatebirds and Masked Boobies on Henderson Island, South Pacific". Condor. 96 (2): 331–340. doi:10.2307/1369318. JSTOR 1369318. S2CID 8846837.
42. Croxall, J. P. & Prince, P. A. (1994). "Dead or alive, night or day: how do albatrosses catch squid?". Antarctic Science. 6 (2): 155–162. Bibcode:1994AntSc...6..155C. doi:10.1017/S0954102094000246. S2CID 86598155.
43. Punta, G.; Herrera, G. (1995). "Predation by Southern Giant Petrels Macronectes giganteus on adult Imperial Cormorants Phalacrocorax atriceps" (PDF). Marine Ornithology. 23: 166–167.
44. Robertson, C. J. R. (1993). "Survival and longevity of the Northern Royal Albatross Diomedea epomophora sanfordi at Taiaroa Head 1937–93". Emu. 93 (4): 269–276. doi:10.1071/MU9930269.
45. Manuwal, D. A. and Thoresen, A. C. (1993). Cassin's Auklet (Ptychoramphus aleuticus). In The Birds of North America, No. 50 (A. Poole and F. Gill, eds.). Philadelphia: The Academy of Natural Sciences; Washington, D.C.: The American Ornithologists' Union
46. See Skutch; Alexander Frank (author) and Gardner, Dana (illustrator) Helpers at birds' nests : a worldwide survey of cooperative breeding and related behavior; pp. 69–71. Published 1987 by University of Iowa Press. ISBN 0-87745-150-8
47. Metz, V. G. and Schreiber, E. A. (2002) "Great Frigatebird (Fregata minor)" In The Birds of North America, No 681, (Poole, A. and Gill, F., eds) The Birds of North America Inc.: Philadelphia
48. Pickering, S. P. C. & Berrow, S. D. (2001). "Courtship behaviour of the Wandering Albatross Diomedea exulans at Bird Island, South Georgia" (PDF). Marine Ornithology. 29: 29–37.
49. Schreiber, E. A., Feare, C. J., Harrington, B. A., Murray, B. G., Jr., Robertson, W. B., Jr., Robertson, M. J. and Woolfenden, G. E. (2002). Sooty Tern (Sterna fuscata). In The Birds of North America, No. 665 (A. Poole and F. Gill, eds.). The Birds of North America, Inc., Philadelphia, PA
50. Seto, N. W. H. and O'Daniel, D. (1999) Bonin Petrel (Pterodroma hypoleuca). In The Birds of North America, No. 385 (A. Poole and F. Gill, eds.). The Birds of North America, Inc., Philadelphia, PA
51. Bried, J. L.; Pontier, D.; Jouventin, P. (2003). "Mate fidelity in monogamous birds: a re-examination of the Procellariiformes". Animal Behaviour. 65: 235–246. doi:10.1006/anbe.2002.2045. S2CID 53169037.
52. Fisher, H. I. (1976). "Some dynamics of a breeding colony of Laysan Albatrosses". Wilson Bulletin. 88 (1): 121–142. JSTOR 4160718.
53. Rabouam, C.; Thibault, J.-C.; Bretagnole, V. (1998). "Natal Philopatry and close inbreeding in Cory's shearwater (Calonectris diomedea)" (PDF). Auk. 115 (2): 483–486. doi:10.2307/4089209. JSTOR 4089209.
54. Moors, P. J.; Atkinson, I. A. E. (1984). Predation on seabirds by introduced animals, and factors affecting its severity. In Status and Conservation of the World's Seabirds. Cambridge: ICBP. ISBN 0-946888-03-5
55. Keitt, B. S.; Tershy, B. R.; Croll, D. A. (2004). "Nocturnal behavior reduces predation pressure on Black-vented Shearwaters Puffinus opisthomelas" (PDF). Marine Ornithology. 32 (3): 173–178.
56. Bolton, Mark; Conolly, Georgia; Carroll, Matthew; Wakefield, Ewan D.; Caldow, Richard (2019). "A review of the occurrence of inter-colony segregation of seabird foraging areas and the implications for marine environmental impact assessment". Ibis. 161 (2): 241–259. doi:10.1111/ibi.12677. ISSN 1474-919X.
57. Burness, G. P., Lefevre, K. and Collins, C. T. (1999). Elegant Tern (Sterna elegans). In The Birds of North America, No. 404 (A. Poole and F. Gill, eds.). The Birds of North America, Inc., Philadelphia, PA
58. Shaffer, S. A.; Tremblay, Y.; Weimerskirch, H.; Scott, D.; Thompson, D. R.; Sagar, P. M.; Moller, H.; Taylor, G. A.; Foley, D. G.; Block, B. A.; Costa, D. P. (2006). "Migratory shearwaters integrate oceanic resources across the Pacific Ocean in an endless summer". Proceedings of the National Academy of Sciences. 103 (34): 12799–12802. Bibcode:2006PNAS..10312799S. doi:10.1073/pnas.0603715103. PMC 1568927. PMID 16908846.
59. Oro, D.; Cam, E.; Pradel, R.; Martinetz-Abrain, A. (2004). "Influence of food availability on demography and local population dynamics in a long-lived seabird". Proceedings of the Royal Society B. 271 (1537): 387–396. doi:10.1098/rspb.2003.2609. PMC 1691609. PMID 15101698.
60. Winkler, David W.; Billerman, Shawn M.; Lovette, Irby J. (March 4, 2020), Billerman, Shawn M.; Keeney, Brooke K.; Rodewald, Paul G.; Schulenberg, Thomas S. (eds.), "Northern Storm-Petrels (Hydrobatidae)", Birds of the World, Cornell Lab of Ornithology, doi:10.2173/bow.hydrob1.01, S2CID 216364538, retrieved April 23, 2022
61. Carboneras, Carles; Jutglar, Francesc; Kirwan, Guy M. (2020). "Common Diving-Petrel (Pelecanoides urinatrix), version 1.0". Birds of the World. doi:10.2173/bow.codpet1.01. S2CID 226017737.
62. Orta, Jaume; Christie, David; Jutglar, Francesc; Kirwan, Guy M. (March 4, 2020), Billerman, Shawn M.; Keeney, Brooke K.; Rodewald, Paul G.; Schulenberg, Thomas S. (eds.), "Little Black Cormorant (Phalacrocorax sulcirostris)", Birds of the World, Cornell Lab of Ornithology, doi:10.2173/bow.libcor1.01, S2CID 226397614, retrieved April 22, 2022
63. Croxall, J; Steele, W.; McInnes, S.; Prince, P. (1995). "Breeding Distribution of Snow Petrel Pagodroma nivea" (PDF). Marine Ornithology. 23: 69–99.
64. Nelson, S. K. (1997). Marbled Murrelet (Brachyramphus marmoratus). In The Birds of North America, No. 276 (A. Poole and F. Gill, eds.). The Academy of Natural Sciences, Philadelphia, PA, and The American Ornithologists' Union, Washington, D.C
65. Winkler, D. W. (1996). California Gull (Larus californicus). In The Birds of North America, No. 259 (A. Poole and F. Gill, eds.). The Academy of Natural Sciences, Philadelphia, PA, and The American Ornithologists' Union, Washington, D.C.
66. Wiley, R. Haven; Lee, David S. (March 4, 2020). "Parasitic Jaeger (Stercorarius parasiticus), version 1.0". Birds of the World. Cornell Lab of Ornithology. doi:10.2173/bow.parjae.01. S2CID 216364499. Retrieved March 26, 2021.
67. Harris, M. & Wanless, S. (1996). "Differential responses of Guillemot Uria aalge and Shag Phalacrocorax aristotelis to a late winter wreck". Bird Study. 43 (2): 220–230. doi:10.1080/00063659609461014.
68. Perkins, Sid (January 23, 2018). "Bird poop brings 3.8 million metric tons of nitrogen out of the sea each year". Science Magazine. American Association for the Advancement of Science. Retrieved March 26, 2021.
69. Collis, K.; Adamany, S. – Columbia River Inter-Tribal Fish Commission, Roby, D. D.; Craig, D. P.; Lyons, D. E.; Oregon Cooperative Fish and Wildlife Research Unit, (2000), "Avian Predation on Juvenile Salmonids in the Lower Columbia River", 1998 Annual Report to Bonneville Power Administration, Portland, OR
70. Oro, D.; Ruiz, X.; Pedrocchi, V.; Gonzalez-Solis, J. (1997). "Diet and adult time budgets of Audouin's Gull Larus audouinii in response to changes in commercial fisheries". Ibis. 139 (4): 631–637. doi:10.1111/j.1474-919X.1997.tb04685.x.
71. Thompson, P. M. (2004). Identifying drivers of change; did fisheries play a role in the spread of North Atlantic fulmars? December 17, 2008, at the Wayback Machine in Management of marine ecosystems: monitoring change in upper trophic levels. Cambridge: Cambridge University Press
72. Brooke, Michael (2018). Far From Land: The Mysterious Lives of Seabirds. Princeton: Princeton University Press. p. 197. ISBN 978-0-691-17418-1.
73. "Save the Albatross: The Problem". BirdLife International/RSPB. 2005.
74. Brothers, Nigel (1991). "Albatross mortality and associated bait loss in the Japanese longline fishery in the southern ocean". Biological Conservation. 55 (3): 255–268. doi:10.1016/0006-3207(91)90031-4.
75. Cury, P. M.; Boyd, I. L.; Bonhommeau, S.; Anker-Nilssen, T.; Crawford, R. J. M.; Furness, R. W.; Mills, J. A.; Murphy, E. J.; Osterblom, H.; Paleczny, M.; Piatt, J. F.; Roux, J.-P.; Shannon, L.; Sydeman, W. J. (December 23, 2011). "Global seabird response to forage fish depletion—one-third for the birds" (PDF). Science. 334 (6063): 1703–1706. Bibcode:2011Sci...334.1703C. doi:10.1126/science.1212928. JSTOR 41352310. PMID 22194577. S2CID 1855657.
76. King, Sd; Harper, Ga; Wright, Jb; McInnes, Jc; van der Lubbe, Je; Dobbins, Ml; Murray, Sj (October 25, 2012). "Site-specific reproductive failure and decline of a population of the Endangered yellow-eyed penguin: a case for foraging habitat quality". Marine Ecology Progress Series. 467: 233–244. Bibcode:2012MEPS..467..233K. doi:10.3354/meps09969.
77. Simeone, A. & Navarro, X. (2002). "Human exploitation of seabirds in coastal southern Chile during the mid-Holocene". Rev. Chil. Hist. Nat. 75 (2): 423–431. doi:10.4067/S0716-078X2002000200012.
78. Anderson, A. (1996). "Origins of Procellariidae hunting in the Southwest Pacific". International Journal of Osteoarcheology. 6 (4): 403–410. doi:10.1002/(SICI)1099-1212(199609)6:4<403::AID-OA296>3.0.CO;2-0.
79. White, Peter (1995), The Farallon Islands, Sentinels of the Golden Gate, Scottwall Associates: San Francisco, ISBN 0-942087-10-0
80. "Tītī traditions". University of Otago. Retrieved October 13, 2020.
81. Burnham, W.; Burnham, K. K.; Cade, T. J. (2005). "Past and present assessments of bird life in Uummannaq District, West Greenland" (PDF). Dansk Orn. Foren. Tidsskr. 99: 196–208.
82. Carlile, N.; Proiddel, D.; Zino, F.; Natividad, C.; Wingate, D. B. (2003). "A review of four successful recovery programmes for threatened sub-tropical petrels" (PDF). Marine Ornithology. 31: 185–192.
83. Beale, Colin M.; Monaghan, Pat (April 2004). "Human disturbance: people as predation-free predators?". Journal of Applied Ecology. 41 (2): 335–343. doi:10.1111/j.0021-8901.2004.00900.x.
84. Watson, Hannah; Bolton, Mark; Monaghan, Pat (June 2014). "Out of sight but not out of harm's way: Human disturbance reduces reproductive success of a cavity-nesting seabird". Biological Conservation. 174 (100): 127–133. doi:10.1016/j.biocon.2014.03.020. PMC 4039997. PMID 24899731.
85. Fry, D. & Toone, C. (1981). "DDT-induced feminization of gull embryos". Science. 213 (4510): 922–924. Bibcode:1981Sci...213..922F. doi:10.1126/science.7256288. PMID 7256288.
86. Dunnet, G.; Crisp, D.; Conan, G.; Bourne, W. (1982). "Oil Pollution and Seabird Populations [and Discussion]". Philosophical Transactions of the Royal Society B. 297 (1087): 413–427. Bibcode:1982RSPTB.297..413D. doi:10.1098/rstb.1982.0051.
87. "Species factsheet: Brachyramphus marmoratus". BirdLife International Data Zone. BirdLife International. 2021. Retrieved March 31, 2021.
88. Hagen, Christina (December 12, 2017). "The ultimate irony: Cape Gannets, famed for their greed, are now starving". BirdLife International. Retrieved March 31, 2021.
89. Dias, Maria P.; Martin, Rob; Pearmain, Elizabeth J.; Burfield, Ian J.; Small, Cleo; Phillips, Richard A.; Yates, Oliver; Lascelles, Ben; Borboroglu, Pablo Garcia; Croxall, John P. (2019). "Threats to seabirds: A global assessment". Biological Conservation. 237: 525–537. doi:10.1016/j.biocon.2019.06.033. ISSN 0006-3207. S2CID 201204878.
90. Bindoff, N. L.; Cheung, W. W. L.; Kairo, J. G.; Arístegui, J.; et al. (2019). "Chapter 5: Changing Ocean, Marine Ecosystems, and Dependent Communities" (PDF). Special Report: The Ocean and Cryosphere in a Changing Climate. p. 479.
91. "History of Pelican Island". USFWS Pelican Island National Wildlife Refuge.
92. "About Capricornia Cays". Department of National Parks, Recreation, Sport and Racing. June 7, 2011. Retrieved March 30, 2021.
93. Corday, Chris (2017). "Forbidden Island". CBC. Toronto. Retrieved March 30, 2021.
94. Williams, J. C.; Byrd G. V.; Konyukhov, N. B. (2003). "Whiskered Auklets Aethia pygmaea, foxes, humans and how to right a wrong" (PDF). Marine Ornithology. 31: 175–180.
95. "Stamps celebrate seabird return". BirdLife International. 2005.
96. Food and Agriculture Organisation (1999). The incidental catch of seabirds by longline fisheries: worldwide review and technical guidelines for mitigation June 29, 2006, at the Wayback Machine. FAO Fisheries Circular No.937. Food and Agriculture Organization of the United Nations, Rome
97. Yorio, Pablo; Frere, Esteban; Gandini, Patricia; Schiavini, Adrián (December 2001). "Tourism and recreation at seabird breeding sites in Patagonia, Argentina: current concerns and future prospects". Bird Conservation International. 11 (4): 231–245. doi:10.1017/S0959270901000314.
98. "Ending Seabird Bycatch". BirdLife International. BirdLife International. 2021. Retrieved April 1, 2021.
99. Wiedenfeld, D.A. (2016). "Seabird Bycatch Solutions for Fishery Sustainability" (PDF). American Bird Conservancy. American Bird Conservancy. Retrieved April 1, 2021.
100. Cutlip, Kimbra (August 2, 2017). "Mitigating Seabird Bycatch with Global Fishing Watch". Global Fishing Watch. Retrieved April 1, 2021.
101. "Agreement on the Conservation of Albatrosses and Petrels Site". Australian Antarctic Division. Retrieved March 20, 2021.
102. Carboneras, C. (1992). "Family Diomedeidae (Albatrosses)". In del Hoyo, J.; Elliott, A.; Sargatal, J. (eds.). Handbook of the Birds of the World. Vol. 1: Ostrich to Ducks. Barcelona, Spain: Lynx Edicions. pp. 198–215. ISBN 84-87334-10-5.
103. Cocker, Mark; Mabey, Richard (2005). Birds Britannica. London: Chatto and Windus. p. 10. ISBN 978-0-7011-6907-7.
104. Carboneras, C. (1992). "Family Hydrobatidae (Storm-petrels)". In del Hoyo, J.; Elliott, A.; Sargatal, J. (eds.). Handbook of the Birds of the World. Vol. 1: Ostrich to Ducks. Barcelona, Spain: Lynx Edicions. pp. 258–271. ISBN 84-87334-10-5.

Further reading

• Furness, R. W. (2012). Seabird Ecology. Springer Science & Business Media. ISBN 978-1-4613-2093-7.

External links

•   Media related to Seabirds at Wikimedia Commons

 

Look up seabird in Wiktionary, the free dictionary.

• Seabirds.net: A data portal for global seabird databases and information outlet for the World Seabird Union
• BirdLife International; Save the Albatross Campaign
• Marine Ornithology, the Journal of Seabird Science and Conservation