The common tern ( Sterna hirundo) is a seabird in the family Laridae. This bird has a circumpolar distribution, its four subspecies breeding in Temperateness and subarctic regions of Europe, Asia and North America. It is strongly bird migration, wintering in coastal Tropics and Subtropics regions. Breeding adults have light grey upperparts, white to very light grey underparts, a black cap, orange-red legs, and a narrow pointed bill. Depending on the subspecies, the bill may be mostly red with a black tip or all black. There are several similar species, including the partly Sympatry Arctic tern, which can be separated on plumage details, leg and bill colour, or vocalisations.
Breeding in a wider range of habitats than any of its relatives, the common tern nests on any flat, poorly vegetated surface close to water, including beaches and islands, and it readily adapts to artificial substrates such as floating rafts. The nest may be a bare scrape in sand or gravel, but it is often lined or edged with whatever debris is available. Up to three eggs may be laid, their dull colours and blotchy patterns providing camouflage on the open beach. Incubation is by both sexes, and the eggs hatch in around 21–22 days, longer if the colony is disturbed by predators. The downy chicks fledge in 22–28 days. Like most terns, this species feeds by plunge-diving for fish, either in the sea or in freshwater, but Mollusca, and other invertebrate prey may form a significant part of the diet in some areas.
Eggs and young are vulnerable to predation by mammals such as and American mink, and large birds including , and . Common terns may be infected by lice, , and , although Haematozoa appear to be rare. Its large population and huge breeding range mean that this species is classed as being of least concern, although numbers in North America have declined sharply in recent decades. Despite international legislation protecting the common tern, in some areas, populations are threatened by habitat loss, pollution, or the disturbance of Bird colony.
The common tern's closest relatives appear to be the Antarctic tern, followed by the Arctic and . evidence suggests that the common tern may have diverged from an ancestral stock earlier than its relatives. No are known from North America, and those claimed in Europe are of uncertain age and species.
The common tern was first described by Carl Linnaeus in his landmark 1758 10th edition of Systema Naturae under its current scientific name, Sterna hirundo. "Stearn" was used in Old English, and a similar word was used by the Frisians for the birds. Library subscription required. "Stearn" appears in the poem The Seafarer, written around 1000 A.D. Linnaeus adopted this word for the genus name Sterna. The Latin for swallow is hirundo, and refers here to the tern's superficial likeness to that unrelated bird, which has a similar light build and long forked tail.Hume (1993) pp. 12–13. This resemblance also leads to the informal name "sea swallow", recorded from at least the seventeenth century. The Scots language names picktarnie, SND: Pictarnie tarrock SND: tarrock and their many variants are also believed to be Onomatopoeia, derived from the distinctive call. Because of the difficulty in distinguishing the two species, all the informal common names are shared with the Arctic tern.Cocker & Mabey (2005) pp. 246–247. There was some uncertainty whether Sterna hirundo should apply to the common tern or the arctic tern as the species are very similar and both occur in Sweden. In 1913, the Swedish zoologist Einar Lönnberg concluded that the binomial name Sterna hirundo applied to the common tern.
Four subspecies of the common tern are generally recognized, although S.h.minussensis is sometimes considered an Intergradation between S.h.hirundo and S.h.longipennis.Hume (1993) pp. 88–89.
Juvenile common terns have pale grey upper wings with a dark carpal bar. The crown and nape are brown, and the forehead is ginger, wearing to white by autumn. The upper parts are ginger with brown and white scaling, and the tail lacks the adult's long outer feathers. Birds in their first post-juvenile plumage, which normally remain in their wintering areas, resemble the non-breeding adult, but have a duskier crown, dark carpal bar, and often very worn plumage. By their second year, most young terns are either indistinguishable from adults, or show only minor differences such as a darker bill or white forehead.
The common tern is an agile flyer, capable of rapid turns and swoops, hovering, and vertical take-off. When commuting with fish, it flies close to the surface in a strong head wind, but above the water in a following wind. Unless migrating, normally it stays below , and averages in the absence of a tail wind. Its average flight speed during the nocturnal migration flight is at a height of .
Terns are unusual in the frequency in which they moult their primaries, which are replaced at least twice, occasionally three times in a year. The visible difference in feather age is accentuated in the greater ultraviolet reflectance of new primaries, and the freshness of the wing feathers is used by females in mate selection. Experienced females favour mates which best show their fitness through the quality of their wing feathers. Rarely, a very early moult at the nesting colony is linked to breeding failure, both the onset of moult and reproductive behaviour being linked to falling levels of the hormone prolactin.
In the breeding areas, the roseate tern can be distinguished by its pale plumage, long, mainly black bill and very long tail feathers.van Duivendijk (2011) pp. 200–202. The non-breeding plumage of roseate is pale above and white, sometimes pink-tinged, below. It retains the long tail streamers, and has a black bill.Olsen & Larsson (1995) pp. 69–76. In flight, the roseate's heavier head and neck, long bill and faster, stiffer wingbeats are also characteristic.Blomdahl et al. (2007) p. 340. It feeds further out to sea than the common tern. In North America, the Forster's tern in breeding plumage is obviously larger than the common, with relatively short wings, a heavy head and thick bill, and long, strong legs; in all non-breeding plumages, its white head and dark eye patch make the American species unmistakable.Olsen & Larrson (1995) pp. 103–110.
In the wintering regions, there are also confusion species, including the Antarctic tern of the southern oceans, the South American tern, the white-fronted tern and the white-cheeked tern of the Indian Ocean. The plumage differences due to "opposite" breeding seasons may aid in identification. The Antarctic tern is more sturdy than the common, with a heavier bill. In breeding condition, its dusky underparts and full black cap outline a white cheek stripe. In non-breeding plumages, it lacks, or has only an indistinct, carpal bar, and young birds show dark bars on the tertials, obvious on the closed wing and in flight.Enticott & Tipling (2002) p. 196.Sinclair et al. (2002) p. 212. The South American tern is larger than the common, with a larger, more curved red bill, and has a smoother, more extensive black cap in non-breeding plumage.Schulenberg et al. (2010) p. 154. Like Antarctic, it lacks a strong carpal bar in non-breeding plumages, and it also shares the distinctive barring of the tertials in young birds.Enticott & Tipling (2002) p. 192. The white-fronted tern has a white forehead in breeding plumage, a heavier bill, and in non-breeding plumage is paler below than the common, with white underwings. The white-cheeked tern is smaller, has uniform grey upperparts, and in breeding plumage is darker above with whiter cheeks.Grimmett et al. (1999) pp. 140–141.
Juvenile common terns are easily separated from similar-aged birds of related species. They show extensive ginger colouration to the back, and have a pale base to the bill. Young Arctic terns have a grey back and black bill, and juvenile roseate terns have a distinctive scalloped "saddle".Vinicombe et al. (1990) pp. 133–138. Hybrids between common and roseate terns have been recorded, particularly from the US, and the intermediate plumage and calls shown by these birds is a potential identification pitfall. Such birds may have more extensive black on the bill, but confirmation of mixed breeding may depend on the exact details of individual flight feathers.
Parents and chicks can locate one another by call, and also recognise each other's vocalisations from about the twelfth day from hatching, which helps to keep the brood together.
New World birds winter along both coasts of Central and South America, to Argentina on the east coast and to northern Chile on the west coast.Harrison (1998) pp. 370–374.Cuthbert (2003) p. 4. Records from South America and the Azores show that some birds may cross the Atlantic in both directions on their migration.Lima (2006) p. 132.
The common tern breeds across most of Europe, with the highest numbers in the north and east of the continent. There are small populations on the north African coast, and in the Azores, Canary Islands and Madeira. Most winter off western or southern Africa, birds from the south and west of Europe tending to stay north of the equator and other European birds moving further south.Snow & Perrin (1998) pp. 779–782. The breeding range continues across the temperate and taiga zones of Asia, with scattered outposts on the Persian Gulf and the coast of Iran.Hume (1993) pp. 39–41. Small populations breed on islands off Sri Lanka, and in the Ladakh region of the Tibetan plateau.Rasmussen & Anderton (2005) pp. 194–195. Western Asian birds winter in the northern Indian Ocean, and S.h.tibetana appears to be common off East Africa during the Northern Hemisphere winter.Zimmerman et al. (2010) p. 354. Birds from further north and east in Asia, such as S.h.longipennis, move through Japan, Thailand and the western Pacific Ocean as far as southern Australia. There are small and erratic colonies in West Africa, in Nigeria and Guinea-Bissau, unusual in that they are within what is mainly a wintering area. Only a few common terns have been recorded in New Zealand,Robertson & Heather (2005) p. 126. and this species' status in Polynesia is unclear.Watling (2003) pp. 204–205. A bird Bird ringing at the nest in Sweden was found dead on Stewart Island, New Zealand, five months later, having flown an estimated 25,000km (15,000mi).Newton (2010) pp. 150–151.
As long-distance migrants, common terns sometimes occur well outside their normal range. Stray birds have been found inland in Africa (Zambia and Malawi), and on the Maldives and Comoros islands; the nominate subspecies has reached Australia,Simpson & Day (2010) p. 110. the Andes, and the interior of South America. Asian S.h.longipennis has recent records from western Europe.
The common tern breeds over a wider range of habitats than any of its relatives, nesting from the taiga of Asia to tropical shores,Hume (1993) pp. 30–37. and at altitudes up to in Armenia, and in Asia. It avoids areas which are frequently exposed to excessive rain or wind, and also icy waters, so it does not breed as far north as the Arctic tern. The common tern breeds close to freshwater or the sea on almost any open flat habitat, including sand or , firm dune areas, salt marsh, or, most commonly, islands. Flat grassland or heath, or even large flat rocks may be suitable in an island environment. In mixed colonies, common terns will tolerate somewhat longer ground vegetation than Arctic terns, but avoid the even taller growth acceptable to roseate terns; the relevant factor here is the different leg lengths of the three species. Common terns adapt readily to artificial floating rafts, and may even nest on flat factory roofs. Unusual nest sites include hay bales, a stump above the water, and floating logs or vegetation. There is a record of a common tern taking over a spotted sandpiper nest and laying its eggs with those of the wader. Outside the breeding season, all that is needed in terms of habitat is access to fishing areas, and somewhere to land. In addition to natural beaches and rocks, boats, buoys and piers are often used both as perches and as night-time roosts.
On their return to the breeding sites, the terns may loiter for a few days before settling into a territory, and the actual start of nesting may be linked to a high availability of fish. Terns defend only a small area, with distances between nests sometimes being as little as , although is more typical. As with many birds, the same site is re-used year after year, with a record of one pair returning for 17 successive breeding seasons. Around ninety per cent of experienced birds reuse their former territory, so young birds must nest on the periphery, find a bereaved mate, or move to another colony.Hume (1993) pp. 86–90. A male selects a nesting territory a few days after his arrival in the spring, and is joined by his previous partner unless she is more than five days late, in which case the pair may separate.
Inbreeding among close S. hirundo relatives appears to be avoided passively by immigration and dispersal rather than by kin recognition and
The defence of the territory is mainly by the male, who repels intruders of either sex. He gives an alarm call, opens his wings, raises his tail and bows his head to show the black cap. If the intruder persists, the male stops calling and fights by bill grappling until the intruder submits by raising its head to expose the throat. Aerial trespassers are simply attacked, sometimes following a joint upward spiralling flight. Despite the aggression shown to adults, wandering chicks are usually tolerated, whereas in a gull colony they would be attacked and killed. The nest is defended until the chicks have fledged, and all the adults in the colony will collectively repel potential predators.
Terns are expert at locating their nests in a large colony. Studies show that terns can find and excavate their eggs when they are buried, even if the nest material is removed and the sand smoothed over. They will find a nest placed from its original site, or even further if it is moved in several stages. Eggs are accepted if reshaped with plasticine or coloured yellow (but not red or blue). This ability to locate the eggs is an adaptation to life in an unstable, wind-blown and tidal environment.
The peak time for egg production is early May, with some birds, particularly first-time breeders, laying later in the month or in June. The clutch size is normally three eggs; larger clutches probably result from two females laying in the same nest. Egg size averages , although each successive egg in a clutch is slightly smaller than the first laid. The average egg weight is , of which five per cent is shell. The egg weight depends on how well-fed the female is, as well as on its position in the clutch. The eggs are cream, buff, or pale brown, marked with streaks, spots or blotches of black, brown or grey which help to camouflage them. Incubation is by both sexes, although more often by the female, and lasts 21–22 days, extending to 25days if there are frequent disturbances at the colony which cause the adults to leave the eggs unattended; nocturnal predation may lead to incubation taking up to 34days. On hot days the incubating parent may fly to water to wet its belly feathers before returning to the eggs, thus affording the eggs some cooling. Except when the colony suffers disaster, ninety per cent of the eggs hatch. The precocial down feather chick is yellowish with black or brown markings, and like the eggs, is similar to the equivalent stage of the Arctic tern.Hume & Pearson (1993) pp. 121–124. The chicks fledge in 22–28 days, usually 25–26. Fledged juveniles are fed at the nest for about five days, and then accompany the adults on fishing expeditions. The young birds may receive supplementary feeds from the parents until the end of the breeding season, and beyond. Common terns have been recorded feeding their offspring on migration and in the wintering grounds, at least until the adults move further south in about December.Hume (1993) pp. 120–123.
Like many terns, this species is very defensive of its nest and young, and will harass humans, dogs, and most Diurnality birds, but unlike the more aggressive Arctic tern, it rarely hits the intruder, usually swerving off at the last moment. Adults can discriminate between individual humans, attacking familiar people more intensely than strangers. Nocturnal predators do not elicit similar attacks; colonies can be wiped out by rats, and adults desert the colony for up to eight hours when great horned owls are present.
Common terns usually breed once a year. Second clutches are possible if the first is lost. Rarely, a second clutch may be laid and incubated while some chicks from the first clutch are still being fed. The first breeding attempt is usually at four years of age, sometimes at three years. The average number of young per pair surviving to fledging can vary from zero in the event of the colony being flooded to over 2.5 in a good year. In North America, productivity was between 1.0 and 2.0 on islands, but less than 1.0 at coastal and inland sites. Birds become more successful at raising chicks with age. This continues throughout their breeding lives, but the biggest increase is in the first five years. The maximum documented lifespan in the wild is 23years in North America and 33years in Europe, but twelve years is a more typical lifespan.
Terns have red oil droplets in the of the of their eyes. This improves contrast and sharpens distance Bird vision, especially in hazy conditions.Sinclair (1985) pp. 93–95. Birds that have to see through an air/water interface, such as terns and gulls, have more strongly coloured carotenoid in the cone oil drops than other avian species.Varela, F J; Palacios, A G; Goldsmith T M (1993) "Vision, Brain, and Behavior in Birds" in Zeigler & Bischof (1993) pp. 77–94. The improved eyesight helps terns to locate shoals of fish, although it is uncertain whether they are sighting the phytoplankton on which the fish feed, or observing other terns diving for food.Lythgoe (1979) pp. 180–183. Tern's eyes are not particularly ultraviolet sensitive, an adaptation more suited to terrestrial feeders like the gulls.
The common tern preferentially hunts fish long.Sandilands (2005) pp. 157–160. The species caught depend on what is available, but if there is a choice, terns feeding several chicks will take larger prey than those with smaller broods.Stephens et al. (2007) p. 295. The proportion of fish fed to chicks may be as high as ninety-five per cent in some areas, but invertebrate prey may form a significant part of the diet elsewhere. This may include Annelid, , Mollusca such as small squid, and (, shrimp and Hippoidea). In freshwater areas, large may be caught, such as , and . Adult insects may be caught in the air, and picked from the ground or from the water surface. Prey is caught in the bill and either swallowed head-first, or carried back to the chicks. Occasionally, two or more small fish may be carried simultaneously. When adults take food back to the nest, they recognise their young by call, rather than visual identification.
The common tern may attempt to steal fish from Arctic terns, but might itself be harassed by kleptoparasitism skuas, , roseate terns, or by other common terns while bringing fish back to its nest. In one study, two males whose mates had died spent much time stealing food from neighbouring broods.
Terns normally drink in flight, usually taking seawater in preference to freshwater, if both are available. Chicks do not drink before fledging, reabsorbing water, and, like adults, excreting excess salt in a concentrated solution from a specialised nasal gland.Karleskint (2009) p. 317. Fish bones and the hard of crustaceans or insects are regurgitated as pellets. Adults fly off the nest to Defecation, and even small chicks walk a short distance from the scrape to deposit their Feces. Adults attacking animals (including humans) will often defecate as they dive, often successfully fouling the intruder.
The common tern hosts Bird louse, which are quite different from those found in Arctic terns, despite the close relationship of the two birds.Rothschild & Clay (1953 ) p. 135. It may also be infected by parasitic worms, such as the widespread Diphyllobothrium species, the duck parasite Ligula intestinalis, and Schistocephalus species carried initially by fish. Cestoda of the family Cyclophyllidea may also infect this species. The mite Reighardia sternae has been found in common terns from Italy, North America and China.Rothschild & Clay (1953) pp. 194–197. A study of 75 breeding common terns found that none carried blood parasites. Colonies have been affected by Fowl cholera and Psittacosis, and it is possible that the common tern may be threatened in the future by outbreaks of avian influenza to which it is susceptible. In 1961 the common tern was the first wild bird species identified as infected with avian influenza, the H5N3 variant being found in an outbreak of South African birds.
In the nineteenth century, the use of tern feathers and wings in the Hatmaking trade was the main cause of large reductions in common tern populations in both Europe and North America, especially on the Atlantic coasts and inland. Sometimes entire stuffed birds were used to make hats. Numbers largely recovered early in the twentieth century mainly due to legislation and the work of conservation organizations. Although some Eurasian populations are stable, numbers in North America have fallen by more than seventy per cent in the last forty years, and there is an overall negative trend in the global estimates for this species.
Threats come from habitat loss through building, pollution or vegetation growth, or disturbance of breeding birds by humans, vehicles, boats or dogs. Local natural flooding may lead to nest losses, and some colonies are vulnerable to predation by rats and large gulls. Gulls also compete with terns for nest sites. Some birds are hunted in the Caribbean for commercial sale as food. Breeding success may be enhanced by the use of floating nest rafts, manmade islands or other artificial nest sites, and by preventing human disturbance. Overgrown vegetation may be burned to clear the ground, and gulls can be killed or discouraged by deliberate disturbance. Contamination with polychlorinated biphenyls (PCBs) resulted in enhanced levels of feminisation in male embryos, which seemed to disappear prior to fledging, with no effect on colony productivity, but dichlorodiphenyldichloroethylene (DDE), which results from the breakdown of DDT, led to very low levels of successful breeding in some US locations.
The common tern is one of the species to which the Agreement on the Conservation of African-Eurasian Migratory Waterbirds (AEWA) and the US–Canada Migratory Bird Treaty Act of 1918 apply. Parties to the AEWA agreement are required to engage in a wide range of conservation strategies described in a detailed action plan. The plan is intended to address key issues such as species and habitat conservation, management of human activities, research, education, and implementation. The North American legislation is similar, although there is a greater emphasis on protection.
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