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The Birds Portal

Birds are a group of warm-blooded vertebrates constituting the class Aves (Latin: [ˈaveːs]), characterised by feathers, toothless beaked jaws, the laying of hard-shelled eggs, a high metabolic rate, a four-chambered heart, and a strong yet lightweight skeleton. Birds live worldwide and range in size from the 5.5 cm (2.2 in) bee hummingbird to the 2.8 m (9 ft 2 in) common ostrich. There are over 11,000 living species and they are split into 44 orders. More than half are passerine or "perching" birds. Birds have wings whose development varies according to species; the only known groups without wings are the extinct moa and elephant birds. Wings, which are modified forelimbs, gave birds the ability to fly, although further evolution has led to the loss of flight in some birds, including ratites, penguins, and diverse endemic island species. The digestive and respiratory systems of birds are also uniquely adapted for flight. Some bird species of aquatic environments, particularly seabirds and some waterbirds, have further evolved for swimming. The study of birds is called ornithology.

Birds are feathered theropod dinosaurs and constitute the only known living dinosaurs. Likewise, birds are considered reptiles in the modern cladistic sense of the term, and their closest living relatives are the crocodilians. Birds are descendants of the primitive avialans (whose members include Archaeopteryx) which first appeared during the Late Jurassic. According to some estimates, modern birds (Neornithes) evolved in the Late Cretaceous or between the Early and Late Cretaceous (100 Ma) and diversified dramatically around the time of the Cretaceous–Paleogene extinction event 66 million years ago, which killed off the pterosaurs and all non-ornithuran dinosaurs.

Many social species preserve knowledge across generations (culture). Birds are social, communicating with visual signals, calls, and songs, and participating in such behaviour as cooperative breeding and hunting, flocking, and mobbing of predators. The vast majority of bird species are socially (but not necessarily sexually) monogamous, usually for one breeding season at a time, sometimes for years, and rarely for life. Other species have breeding systems that are polygynous (one male with many females) or, rarely, polyandrous (one female with many males). Birds produce offspring by laying eggs which are fertilised through sexual reproduction. They are usually laid in a nest and incubated by the parents. Most birds have an extended period of parental care after hatching.

Many species of birds are economically important as food for human consumption and raw material in manufacturing, with domesticated and undomesticated birds being important sources of eggs, meat, and feathers. Songbirds, parrots, and other species are popular as pets. Guano (bird excrement) is harvested for use as a fertiliser. Birds figure throughout human culture. About 120 to 130 species have become extinct due to human activity since the 17th century, and hundreds more before then. Human activity threatens about 1,200 bird species with extinction, though efforts are underway to protect them. Recreational birdwatching is an important part of the ecotourism industry. (Full article...)

  • Image 1 Adult of nominate subspecies in Switzerland The Alpine chough (/ˈtʃʌf/) or yellow-billed chough (Pyrrhocorax graculus) is a bird in the crow family, one of only two species in the genus Pyrrhocorax. Its two subspecies breed in high mountains from Spain eastwards through southern Europe and North Africa to Central Asia and Nepal, and it may nest at a higher altitude than any other bird. The eggs have adaptations to the thin atmosphere that improve oxygen take-up and reduce water loss. This bird has glossy black plumage, a yellow beak, red legs, and distinctive calls. It has a buoyant acrobatic flight with widely spread flight feathers. The Alpine chough pairs for life and displays fidelity to its breeding site, which is usually a cave or crevice in a cliff face. It builds a lined stick nest and lays three to five brown-blotched whitish eggs. It feeds, usually in flocks, on short grazed grassland, taking mainly invertebrate prey in summer and fruit in winter; it will readily approach tourist sites to find supplementary food. Although it is subject to predation and parasitism, and changes in agricultural practices have caused local population declines, this widespread and abundant species is not threatened globally. Climate change may present a long-term threat, by shifting the necessary Alpine habitat to higher altitudes. (Full article...)

    Adult of nominate subspecies in Switzerland

    The Alpine chough (/ˈtʃʌf/) or yellow-billed chough (Pyrrhocorax graculus) is a bird in the crow family, one of only two species in the genus Pyrrhocorax. Its two subspecies breed in high mountains from Spain eastwards through southern Europe and North Africa to Central Asia and Nepal, and it may nest at a higher altitude than any other bird. The eggs have adaptations to the thin atmosphere that improve oxygen take-up and reduce water loss.

    This bird has glossy black plumage, a yellow beak, red legs, and distinctive calls. It has a buoyant acrobatic flight with widely spread flight feathers. The Alpine chough pairs for life and displays fidelity to its breeding site, which is usually a cave or crevice in a cliff face. It builds a lined stick nest and lays three to five brown-blotched whitish eggs. It feeds, usually in flocks, on short grazed grassland, taking mainly invertebrate prey in summer and fruit in winter; it will readily approach tourist sites to find supplementary food.

    Although it is subject to predation and parasitism, and changes in agricultural practices have caused local population declines, this widespread and abundant species is not threatened globally. Climate change may present a long-term threat, by shifting the necessary Alpine habitat to higher altitudes. (Full article...)
  • Image 2 An American white ibis wading in the Tampa Bay area of Florida The American white ibis (Eudocimus albus) is a species of bird in the ibis family, Threskiornithidae. It is found from the southern half of the US East Coast (from southern New Jersey, Virginia, the Carolinas and Georgia), along the Gulf Coast states (Florida, Alabama, Mississippi, Louisiana and Texas) and south through most of the Caribbean coastal regions of Central America. This particular ibis species is a medium-sized wading bird, possessing an overall white plumage with black wing-tips (usually only visible in flight), and having the typical downward-curving bill of the ibises, though of a bright red-orange color, the same hue as its long legs. Males are larger and have longer bills than females. The breeding range runs along the Gulf and Atlantic Coast, and the coasts of Mexico and Central America. Outside the breeding period, the range extends further inland in North America and also includes the Caribbean. It is also found along the northwestern South American coastline in Colombia and Venezuela. Populations in central Venezuela overlap and interbreed with the scarlet ibis. The two have been classified by some authorities as a single species. Their diet consists primarily of small aquatic prey, such as insects and small fishes. Crayfish are its preferred food in most regions, but it can adjust its diet according to the habitat and prey abundance. Its main foraging behavior is probing with its beak at the bottom of shallow water to feel for and capture its prey. It does not see the prey. During the breeding season, the American white ibis gathers in huge colonies near water. Pairs are predominantly monogamous and both parents care for the young, although males tend to engage in extra-pair copulation with other females to increase their reproductive success. Males have also been found to pirate food from unmated females and juveniles during the breeding season. (Full article...)

    An American white ibis wading in the Tampa Bay area of Florida

    The American white ibis (Eudocimus albus) is a species of bird in the ibis family, Threskiornithidae. It is found from the southern half of the US East Coast (from southern New Jersey, Virginia, the Carolinas and Georgia), along the Gulf Coast states (Florida, Alabama, Mississippi, Louisiana and Texas) and south through most of the Caribbean coastal regions of Central America. This particular ibis species is a medium-sized wading bird, possessing an overall white plumage with black wing-tips (usually only visible in flight), and having the typical downward-curving bill of the ibises, though of a bright red-orange color, the same hue as its long legs. Males are larger and have longer bills than females. The breeding range runs along the Gulf and Atlantic Coast, and the coasts of Mexico and Central America. Outside the breeding period, the range extends further inland in North America and also includes the Caribbean. It is also found along the northwestern South American coastline in Colombia and Venezuela. Populations in central Venezuela overlap and interbreed with the scarlet ibis. The two have been classified by some authorities as a single species.

    Their diet consists primarily of small aquatic prey, such as insects and small fishes. Crayfish are its preferred food in most regions, but it can adjust its diet according to the habitat and prey abundance. Its main foraging behavior is probing with its beak at the bottom of shallow water to feel for and capture its prey. It does not see the prey.

    During the breeding season, the American white ibis gathers in huge colonies near water. Pairs are predominantly monogamous and both parents care for the young, although males tend to engage in extra-pair copulation with other females to increase their reproductive success. Males have also been found to pirate food from unmated females and juveniles during the breeding season. (Full article...)
  • Image 3 The elfin woods warbler (Setophaga angelae) is a species of bird endemic to Puerto Rico, where it is local and uncommon. Discovered in 1968 and described in 1972, it is the most recently described New World warbler (family Parulidae). The species name, angelae, is a tribute to Angela Kepler, one of its discoverers. These birds are insectivores, as they feed by gleaning small insects off the habitat leaves. Due to its small populations and restricted habitats, conservation efforts were begun in 1982 to protect this species, but as of 2005, the warbler was still in need of protection. The species is not in immediate danger as the majority of its habitat is protected forest, but introduced species (such as rats and small Asian mongooses), habitat reduction, and natural disasters represent potential threats to the population. (Full article...)

    The elfin woods warbler (Setophaga angelae) is a species of bird endemic to Puerto Rico, where it is local and uncommon. Discovered in 1968 and described in 1972, it is the most recently described New World warbler (family Parulidae).

    The species name, angelae, is a tribute to Angela Kepler, one of its discoverers. These birds are insectivores, as they feed by gleaning small insects off the habitat leaves.

    Due to its small populations and restricted habitats, conservation efforts were begun in 1982 to protect this species, but as of 2005, the warbler was still in need of protection. The species is not in immediate danger as the majority of its habitat is protected forest, but introduced species (such as rats and small Asian mongooses), habitat reduction, and natural disasters represent potential threats to the population. (Full article...)
  • Image 4 Anthus spinoletta spinoletta The water pipit (Anthus spinoletta) is a small passerine bird which breeds in the mountains of Southern Europe and the Palearctic eastwards to China. It is a short-distance migrant; many birds move to lower altitudes or wet open lowlands in winter. The water pipit in breeding plumage has greyish-brown upperparts, weakly streaked with darker brown, and pale pink-buff underparts fading to whitish on the lower belly. The head is grey with a broad white supercilium ("eyebrow"), and the outer tail feathers are white. In winter, the head is grey-brown, the supercilium is duller, the upperparts are more streaked, and the underparts are white, streaked lightly with brown on the breast and flanks. There are only minor differences among the three subspecies, the sexes are almost identical, and young birds resemble adults. The water pipit's song is delivered from a perch or in flight, and consists of four or five blocks, each consisting of about six repetitions of a different short note. Water pipits construct a cup-like nest on the ground under vegetation or in cliff crevices and lay four to six speckled grey-ish white eggs, which hatch in about two weeks with a further 14–15 days to fledging. Although pipits occasionally catch insects in flight, they feed mainly on small invertebrates picked off the ground or vegetation, and also some plant material. (Full article...)

    Anthus spinoletta spinoletta

    The water pipit (Anthus spinoletta) is a small passerine bird which breeds in the mountains of Southern Europe and the Palearctic eastwards to China. It is a short-distance migrant; many birds move to lower altitudes or wet open lowlands in winter.

    The water pipit in breeding plumage has greyish-brown upperparts, weakly streaked with darker brown, and pale pink-buff underparts fading to whitish on the lower belly. The head is grey with a broad white supercilium ("eyebrow"), and the outer tail feathers are white. In winter, the head is grey-brown, the supercilium is duller, the upperparts are more streaked, and the underparts are white, streaked lightly with brown on the breast and flanks. There are only minor differences among the three subspecies, the sexes are almost identical, and young birds resemble adults. The water pipit's song is delivered from a perch or in flight, and consists of four or five blocks, each consisting of about six repetitions of a different short note.

    Water pipits construct a cup-like nest on the ground under vegetation or in cliff crevices and lay four to six speckled grey-ish white eggs, which hatch in about two weeks with a further 14–15 days to fledging. Although pipits occasionally catch insects in flight, they feed mainly on small invertebrates picked off the ground or vegetation, and also some plant material. (Full article...)
  • Image 5 Males in breeding plumage in Diergaarde Blijdorp, the Netherlands The ruff (Calidris pugnax) is a medium-sized wading bird that breeds in marshes and wet meadows across northern Eurasia. This highly gregarious sandpiper is migratory and sometimes forms huge flocks in its winter grounds, which include southern and western Europe, Africa, southern Asia and Australia. The ruff is a long-necked, pot-bellied bird. This species shows marked sexual dimorphism; the male is much larger than the female (the reeve), and has a breeding plumage that includes brightly coloured head tufts, bare orange facial skin, extensive black on the breast, and the large collar of ornamental feathers that inspired this bird's English name. The female and the non-breeding male have grey-brown upperparts and mainly white underparts. Three differently plumaged types of male, including a rare form that mimics the female, use a variety of strategies to obtain mating opportunities at a lek, and the colourful head and neck feathers are erected as part of the elaborate main courting display. The female has one brood per year and lays four eggs in a well-hidden ground nest, incubating the eggs and rearing the chicks, which are mobile soon after hatching, on her own. Predators of wader chicks and eggs include mammals such as foxes, feral cats and stoats, and birds such as large gulls, corvids and skuas. The ruff forages in wet grassland and soft mud, probing or searching by sight for edible items. It primarily feeds on insects, especially in the breeding season, but it will consume plant material, including rice and maize, on migration and in winter. Classified as "least concern" on the IUCN Red List criteria, the global conservation concerns are relatively low because of the large numbers that breed in Scandinavia and the Arctic. However, the range in much of Europe is contracting because of land drainage, increased fertiliser use, the loss of mown or grazed breeding sites, and over-hunting. This decline has seen it listed in the Agreement on the Conservation of African-Eurasian Migratory Waterbirds (AEWA). (Full article...)

    Males in breeding plumage in Diergaarde Blijdorp, the Netherlands

    The ruff (Calidris pugnax) is a medium-sized wading bird that breeds in marshes and wet meadows across northern Eurasia. This highly gregarious sandpiper is migratory and sometimes forms huge flocks in its winter grounds, which include southern and western Europe, Africa, southern Asia and Australia.

    The ruff is a long-necked, pot-bellied bird. This species shows marked sexual dimorphism; the male is much larger than the female (the reeve), and has a breeding plumage that includes brightly coloured head tufts, bare orange facial skin, extensive black on the breast, and the large collar of ornamental feathers that inspired this bird's English name. The female and the non-breeding male have grey-brown upperparts and mainly white underparts. Three differently plumaged types of male, including a rare form that mimics the female, use a variety of strategies to obtain mating opportunities at a lek, and the colourful head and neck feathers are erected as part of the elaborate main courting display. The female has one brood per year and lays four eggs in a well-hidden ground nest, incubating the eggs and rearing the chicks, which are mobile soon after hatching, on her own. Predators of wader chicks and eggs include mammals such as foxes, feral cats and stoats, and birds such as large gulls, corvids and skuas.

    The ruff forages in wet grassland and soft mud, probing or searching by sight for edible items. It primarily feeds on insects, especially in the breeding season, but it will consume plant material, including rice and maize, on migration and in winter. Classified as "least concern" on the IUCN Red List criteria, the global conservation concerns are relatively low because of the large numbers that breed in Scandinavia and the Arctic. However, the range in much of Europe is contracting because of land drainage, increased fertiliser use, the loss of mown or grazed breeding sites, and over-hunting. This decline has seen it listed in the Agreement on the Conservation of African-Eurasian Migratory Waterbirds (AEWA). (Full article...)
  • Image 6 A Sandwich tern, a common tern and a roseate tern together, Northumberland, UK Terns are seabirds in the family Laridae, subfamily Sterninae, that have a worldwide distribution and are normally found near the sea, rivers, or wetlands. Terns are treated in eleven genera in a subgroup of the family Laridae, which also includes several genera of gulls and the skimmers (Rynchops). They are slender, lightly built birds with long, forked tails, narrow wings, long bills, and relatively short legs. Most species are pale grey above and white below with a contrasting black cap to the head, but the marsh terns, the black-bellied tern, the Inca tern, and some noddies have dark body plumage for at least part of the year. The sexes are identical in appearance, but young birds are readily distinguishable from adults. Terns have a non-breeding plumage, which usually involves a white forehead and much-reduced black cap. Terns are long-lived birds and are relatively free from natural predators and parasites; most species are declining in numbers due directly or indirectly to human activities, including habitat loss, pollution, disturbance, and predation by introduced mammals. The Chinese crested tern is critically endangered and three other species are classed as endangered. International agreements provide a measure of protection, but adults and eggs of some species are still used for food in the tropics. (Full article...)

    A Sandwich tern, a common tern and a roseate tern together, Northumberland, UK

    Terns are seabirds in the family Laridae, subfamily Sterninae, that have a worldwide distribution and are normally found near the sea, rivers, or wetlands. Terns are treated in eleven genera in a subgroup of the family Laridae, which also includes several genera of gulls and the skimmers (Rynchops). They are slender, lightly built birds with long, forked tails, narrow wings, long bills, and relatively short legs. Most species are pale grey above and white below with a contrasting black cap to the head, but the marsh terns, the black-bellied tern, the Inca tern, and some noddies have dark body plumage for at least part of the year. The sexes are identical in appearance, but young birds are readily distinguishable from adults. Terns have a non-breeding plumage, which usually involves a white forehead and much-reduced black cap.

    Terns are long-lived birds and are relatively free from natural predators and parasites; most species are declining in numbers due directly or indirectly to human activities, including habitat loss, pollution, disturbance, and predation by introduced mammals. The Chinese crested tern is critically endangered and three other species are classed as endangered. International agreements provide a measure of protection, but adults and eggs of some species are still used for food in the tropics. (Full article...)
  • Image 7 C. a. brasiliensis Petén, Guatemala The black vulture (Coragyps atratus), also known as the American black vulture, Mexican vulture, zopilote, urubu, or gallinazo, is a bird in the New World vulture family whose range extends from the southeastern United States to Peru, Central Chile and Uruguay in South America. Although a common and widespread species, it has a somewhat more restricted distribution than its compatriot, the turkey vulture, which breeds well into Canada and all the way south to Tierra del Fuego. It is the only extant member of the genus Coragyps, which is in the family Cathartidae. Despite the similar name and appearance, this species is not closely related to the Eurasian black vulture, an Old World vulture, of the family Accipitridae (which includes raptors like the eagles, hawks, kites, and harriers). For ease of locating animal corpses (their primary source of sustenance), black vultures tend to inhabit relatively open areas with scattered trees, such as chaparral, in addition to subtropical forested areas and parts of the Brazilian pantanal. With a wingspan of 1.5 m (4.9 ft), the black vulture is an imposing bird, though relatively small for a vulture, let alone a raptor. It has black plumage, a featherless, grayish-black head and neck, and a short, hooked beak. These features are all evolutionary adaptations to life as a scavenger; their black plumage stays visibly cleaner than that of a lighter-colored bird, the bare head is designed for easily digging inside animal carcasses, and the hooked beak is built for stripping the bodies clean of meat. The absence of head feathers helps the birds stay clean and remain (more or less) free of animal blood and bodily fluids, which could become problematic for the vultures and attract parasites; most vultures are known to bathe after eating, provided there is a water source. This water source can be natural or man-made, such as a stream or a livestock water tank. The black vulture is a scavenger and feeds on carrion, but will also eat eggs, small reptiles, or small newborn animals (livestock such as cattle, or deer, rodents, rabbits, etc.), albeit very rarely. They will also opportunistically prey on extremely weakened, sick, elderly, or otherwise vulnerable animals. In areas populated by humans, it also scavenges at dumpster sites and garbage dumps. It finds its meals by using its keen eyesight or following other (New World) vultures, which all possess a keen sense of smell. Lacking a syrinx—the vocal organ of birds—its only vocalizations are grunts or low hisses. It lays its eggs in caves, in cliffside rock crevasses, dead and hollow trees, or, in the absence of predators, on the bare ground, generally raising two chicks each year. The parents feed their young by regurgitation from their crop, an additional digestive organ unique to birds, used for storing excess food; their “infant formula”, of sorts, is thus called “crop milk”. In the United States, the vulture receives legal protection under the Migratory Bird Treaty Act of 1918. This vulture also appeared in Mayan codices. (Full article...)

    C. a. brasiliensis
    Petén, Guatemala

    The black vulture (Coragyps atratus), also known as the American black vulture, Mexican vulture, zopilote, urubu, or gallinazo, is a bird in the New World vulture family whose range extends from the southeastern United States to Peru, Central Chile and Uruguay in South America. Although a common and widespread species, it has a somewhat more restricted distribution than its compatriot, the turkey vulture, which breeds well into Canada and all the way south to Tierra del Fuego. It is the only extant member of the genus Coragyps, which is in the family Cathartidae. Despite the similar name and appearance, this species is not closely related to the Eurasian black vulture, an Old World vulture, of the family Accipitridae (which includes raptors like the eagles, hawks, kites, and harriers). For ease of locating animal corpses (their primary source of sustenance), black vultures tend to inhabit relatively open areas with scattered trees, such as chaparral, in addition to subtropical forested areas and parts of the Brazilian pantanal.

    With a wingspan of 1.5 m (4.9 ft), the black vulture is an imposing bird, though relatively small for a vulture, let alone a raptor. It has black plumage, a featherless, grayish-black head and neck, and a short, hooked beak. These features are all evolutionary adaptations to life as a scavenger; their black plumage stays visibly cleaner than that of a lighter-colored bird, the bare head is designed for easily digging inside animal carcasses, and the hooked beak is built for stripping the bodies clean of meat. The absence of head feathers helps the birds stay clean and remain (more or less) free of animal blood and bodily fluids, which could become problematic for the vultures and attract parasites; most vultures are known to bathe after eating, provided there is a water source. This water source can be natural or man-made, such as a stream or a livestock water tank.

    The black vulture is a scavenger and feeds on carrion, but will also eat eggs, small reptiles, or small newborn animals (livestock such as cattle, or deer, rodents, rabbits, etc.), albeit very rarely. They will also opportunistically prey on extremely weakened, sick, elderly, or otherwise vulnerable animals. In areas populated by humans, it also scavenges at dumpster sites and garbage dumps. It finds its meals by using its keen eyesight or following other (New World) vultures, which all possess a keen sense of smell. Lacking a syrinx—the vocal organ of birds—its only vocalizations are grunts or low hisses. It lays its eggs in caves, in cliffside rock crevasses, dead and hollow trees, or, in the absence of predators, on the bare ground, generally raising two chicks each year. The parents feed their young by regurgitation from their crop, an additional digestive organ unique to birds, used for storing excess food; their “infant formula”, of sorts, is thus called “crop milk”. In the United States, the vulture receives legal protection under the Migratory Bird Treaty Act of 1918. This vulture also appeared in Mayan codices. (Full article...)
  • Image 8 1708 drawing by François Leguat, the only known illustration of this species by someone who observed it alive The Rodrigues solitaire (Pezophaps solitaria) is an extinct flightless bird that was endemic to the island of Rodrigues, east of Madagascar in the Indian Ocean. Genetically within the family of pigeons and doves, it was most closely related to the also extinct dodo of the nearby island Mauritius, the two forming the subfamily Raphinae. The Nicobar pigeon is their closest living genetic relative. Rodrigues solitaires grew to the size of swans, and demonstrated pronounced sexual dimorphism. Males were much larger than females and measured up to 75.7–90 centimetres (30–35 inches) in height and 28 kilograms (62 pounds) in weight, contrasting with 63.8–70 centimetres (25–28 in) and 17 kilograms (37 lb) for females. Its plumage was grey and brown; the female was paler than the male. It had a black band at the base of its slightly hooked beak, and its neck and legs were long. Both sexes were highly territorial, with large bony knobs on their wings that were used in combat. The Rodrigues solitaire laid a single egg that was incubated in turn by both sexes. Gizzard stones helped digest its food, which included fruit and seeds. First mentioned during the 17th century, the Rodrigues solitaire was described in detail by François Leguat, the leader of a group of French Huguenot refugees who were marooned on Rodrigues in 1691–1693. It was hunted by humans and introduced animals, and was extinct by the late 18th century. Apart from Leguat's account and drawing, and a few other contemporary descriptions, nothing was known about the bird until a few subfossil bones were found in a cave in 1786. Thousands of bones have subsequently been excavated. It is the only extinct bird with a former constellation named after it, Turdus Solitarius. (Full article...)

    1708 drawing by François Leguat, the only known illustration of this species by someone who observed it alive

    The Rodrigues solitaire (Pezophaps solitaria) is an extinct flightless bird that was endemic to the island of Rodrigues, east of Madagascar in the Indian Ocean. Genetically within the family of pigeons and doves, it was most closely related to the also extinct dodo of the nearby island Mauritius, the two forming the subfamily Raphinae. The Nicobar pigeon is their closest living genetic relative.

    Rodrigues solitaires grew to the size of swans, and demonstrated pronounced sexual dimorphism. Males were much larger than females and measured up to 75.7–90 centimetres (30–35 inches) in height and 28 kilograms (62 pounds) in weight, contrasting with 63.8–70 centimetres (25–28 in) and 17 kilograms (37 lb) for females. Its plumage was grey and brown; the female was paler than the male. It had a black band at the base of its slightly hooked beak, and its neck and legs were long. Both sexes were highly territorial, with large bony knobs on their wings that were used in combat. The Rodrigues solitaire laid a single egg that was incubated in turn by both sexes. Gizzard stones helped digest its food, which included fruit and seeds.

    First mentioned during the 17th century, the Rodrigues solitaire was described in detail by François Leguat, the leader of a group of French Huguenot refugees who were marooned on Rodrigues in 1691–1693. It was hunted by humans and introduced animals, and was extinct by the late 18th century. Apart from Leguat's account and drawing, and a few other contemporary descriptions, nothing was known about the bird until a few subfossil bones were found in a cave in 1786. Thousands of bones have subsequently been excavated. It is the only extinct bird with a former constellation named after it, Turdus Solitarius. (Full article...)
  • Image 9 A black-shouldered kite at the Royal Botanic Gardens Victoria, Melbourne, Victoria, Australia The black-shouldered kite (Elanus axillaris), also known as the Australian black-shouldered kite, is a small raptor found in open habitats throughout Australia. It resembles similar species found in Africa, Eurasia and North America, including the black-winged kite, a species that has in the past also been called "black-shouldered kite". Measuring around 35 cm (14 in) in length, with a wingspan of 80–100 cm (31–39 in), the adult black-shouldered kite has predominantly grey-white plumage and prominent black markings above its red eyes. It gains its name from the black patches on its wings. The primary call is a clear whistle, uttered in flight and while hovering. It can be confused with the related letter-winged kite in Australia, which is distinguished by the striking black markings under its wings. The species forms monogamous pairs, breeding between August and January. The birds engage in aerial courtship displays which involve high circling flight and ritualised feeding mid-air. Three or four eggs are laid and incubated for around thirty days. Chicks are fully fledged within five weeks of hatching and can hunt for mice within a week of leaving the nest. Juveniles disperse widely from their home territory. The black-shouldered kite hunts in open grasslands, searching for its prey by hovering and systematically scanning the ground. It mainly eats small rodents, particularly the introduced house mouse, and has benefitted from the modification of the Australian landscape by agriculture. It is rated as least concern on the International Union for Conservation of Nature (IUCN)'s Red List of Threatened Species. (Full article...)

    A black-shouldered kite at the Royal Botanic Gardens Victoria, Melbourne, Victoria, Australia

    The black-shouldered kite (Elanus axillaris), also known as the Australian black-shouldered kite, is a small raptor found in open habitats throughout Australia. It resembles similar species found in Africa, Eurasia and North America, including the black-winged kite, a species that has in the past also been called "black-shouldered kite". Measuring around 35 cm (14 in) in length, with a wingspan of 80–100 cm (31–39 in), the adult black-shouldered kite has predominantly grey-white plumage and prominent black markings above its red eyes. It gains its name from the black patches on its wings. The primary call is a clear whistle, uttered in flight and while hovering. It can be confused with the related letter-winged kite in Australia, which is distinguished by the striking black markings under its wings.

    The species forms monogamous pairs, breeding between August and January. The birds engage in aerial courtship displays which involve high circling flight and ritualised feeding mid-air. Three or four eggs are laid and incubated for around thirty days. Chicks are fully fledged within five weeks of hatching and can hunt for mice within a week of leaving the nest. Juveniles disperse widely from their home territory. The black-shouldered kite hunts in open grasslands, searching for its prey by hovering and systematically scanning the ground. It mainly eats small rodents, particularly the introduced house mouse, and has benefitted from the modification of the Australian landscape by agriculture. It is rated as least concern on the International Union for Conservation of Nature (IUCN)'s Red List of Threatened Species. (Full article...)
  • Image 10 Looking south across the reserve, with reed beds in the foreground Ham Wall is an English wetland National Nature Reserve (NNR) 4 kilometres (2.5 mi) west of Glastonbury on the Somerset Levels. It is managed by the Royal Society for the Protection of Birds (RSPB). Since the last Ice Age, decomposing plants in the marshes of the Brue valley in Somerset have accumulated as deep layers of peat that were commercially exploited on a large scale in the twentieth century. Consumer demand eventually declined, and in 1994 the landowners, Fisons, gave their old workings to what is now Natural England, who passed the management of the 260 hectares (640 acres) Ham Wall section to the RSPB. The Ham Wall reserve was constructed originally to provide reed bed habitat for the Eurasian bittern, which at the time was at a very low population level in the UK. The site is divided into several sections with independently controllable water levels, and machinery and cattle are used to maintain the quality of the reed beds. There are important breeding populations of wetland birds including the rare little bittern and great white egret, and the area hosts several other uncommon animals and plants. The RSPB works with other organisations as part of the Avalon Marshes Partnership to coordinate conservation issues across the Somerset Levels. The reserve is open year-round, and has nature trails, hides and viewing points. It lies within the Somerset Levels NNR and the Somerset Levels and Moors' Ramsar and Special Area of Conservation site. Potential future threats may result from increasing unpredictability in the UK climate, leading to heavy summer rains and extensive flooding. Sea level rise will make the drainage of the Levels more difficult, and current water pumping facilities may become inadequate. (Full article...)

    Looking south across the reserve, with reed beds in the foreground

    Ham Wall is an English wetland National Nature Reserve (NNR) 4 kilometres (2.5 mi) west of Glastonbury on the Somerset Levels. It is managed by the Royal Society for the Protection of Birds (RSPB). Since the last Ice Age, decomposing plants in the marshes of the Brue valley in Somerset have accumulated as deep layers of peat that were commercially exploited on a large scale in the twentieth century. Consumer demand eventually declined, and in 1994 the landowners, Fisons, gave their old workings to what is now Natural England, who passed the management of the 260 hectares (640 acres) Ham Wall section to the RSPB.

    The Ham Wall reserve was constructed originally to provide reed bed habitat for the Eurasian bittern, which at the time was at a very low population level in the UK. The site is divided into several sections with independently controllable water levels, and machinery and cattle are used to maintain the quality of the reed beds. There are important breeding populations of wetland birds including the rare little bittern and great white egret, and the area hosts several other uncommon animals and plants. The RSPB works with other organisations as part of the Avalon Marshes Partnership to coordinate conservation issues across the Somerset Levels.

    The reserve is open year-round, and has nature trails, hides and viewing points. It lies within the Somerset Levels NNR and the Somerset Levels and Moors' Ramsar and Special Area of Conservation site. Potential future threats may result from increasing unpredictability in the UK climate, leading to heavy summer rains and extensive flooding. Sea level rise will make the drainage of the Levels more difficult, and current water pumping facilities may become inadequate. (Full article...)
  • Image 11 Georg Forster at age 26, by J. H. W. Tischbein, 1781 Johann George Adam Forster, also known as Georg Forster (German pronunciation: [ˈɡeːɔʁk ˈfɔʁstɐ], 27 November 1754 – 10 January 1794), was a German geographer, naturalist, ethnologist, travel writer, journalist and revolutionary. At an early age, he accompanied his father, Johann Reinhold Forster, on several scientific expeditions, including James Cook's second voyage to the Pacific. His report of that journey, A Voyage Round the World, contributed significantly to the ethnology of the people of Polynesia and remains a respected work. As a result of the report, Forster, who was admitted to the Royal Society at the early age of twenty-two, came to be considered one of the founders of modern scientific travel literature. After returning to continental Europe, Forster turned toward academia. He taught natural history at the Collegium Carolinum in the Ottoneum, Kassel (1778–84), and later at the Academy of Vilna (Vilnius University) (1784–87). In 1788, he became head librarian at the University of Mainz. Most of his scientific work during this time consisted of essays on botany and ethnology, but he also prefaced and translated many books about travel and exploration, including a German translation of Cook's diaries. Forster was a central figure of the Enlightenment in Germany, and corresponded with most of its adherents, including his close friend Georg Christoph Lichtenberg. His ideas, travelogues and personality influenced Alexander von Humboldt, one of the great scientists of the 19th century who hailed Forster as the founder of both comparative ethnology (Völkerkunde) and regional geography (Länderkunde). When the French took control of Mainz in 1792, Forster played a leading role in the Mainz Republic, the earliest republican state in Germany. During July 1793 and while he was in Paris as a delegate of the young Mainz Republic, Prussian and Austrian coalition forces regained control of the city and Forster was declared an outlaw. Unable to return to Germany and separated from his friends and family, he died in Paris of illness in early 1794, not yet 40. (Full article...)

    Georg Forster at age 26, by J. H. W. Tischbein, 1781

    Johann George Adam Forster, also known as Georg Forster (German pronunciation: [ˈɡeːɔʁk ˈfɔʁstɐ], 27 November 1754 – 10 January 1794), was a German geographer, naturalist, ethnologist, travel writer, journalist and revolutionary. At an early age, he accompanied his father, Johann Reinhold Forster, on several scientific expeditions, including James Cook's second voyage to the Pacific. His report of that journey, A Voyage Round the World, contributed significantly to the ethnology of the people of Polynesia and remains a respected work. As a result of the report, Forster, who was admitted to the Royal Society at the early age of twenty-two, came to be considered one of the founders of modern scientific travel literature.

    After returning to continental Europe, Forster turned toward academia. He taught natural history at the Collegium Carolinum in the Ottoneum, Kassel (1778–84), and later at the Academy of Vilna (Vilnius University) (1784–87). In 1788, he became head librarian at the University of Mainz. Most of his scientific work during this time consisted of essays on botany and ethnology, but he also prefaced and translated many books about travel and exploration, including a German translation of Cook's diaries.

    Forster was a central figure of the Enlightenment in Germany, and corresponded with most of its adherents, including his close friend Georg Christoph Lichtenberg. His ideas, travelogues and personality influenced Alexander von Humboldt, one of the great scientists of the 19th century who hailed Forster as the founder of both comparative ethnology (Völkerkunde) and regional geography (Länderkunde).
    When the French took control of Mainz in 1792, Forster played a leading role in the Mainz Republic, the earliest republican state in Germany. During July 1793 and while he was in Paris as a delegate of the young Mainz Republic, Prussian and Austrian coalition forces regained control of the city and Forster was declared an outlaw. Unable to return to Germany and separated from his friends and family, he died in Paris of illness in early 1794, not yet 40. (Full article...)
  • Image 12 Adult and juvenile specimens, Muséum national d'Histoire naturelle, Paris; the juvenile could possibly also be a Kangaroo Island emu The King Island emu (Dromaius novaehollandiae minor) is an extinct subspecies of emu that was endemic to King Island, in the Bass Strait between mainland Australia and Tasmania. Its closest relative may be the also extinct Tasmanian emu (D. n. diemenensis), as they belonged to a single population until less than 14,000 years ago, when Tasmania and King Island were still connected. The small size of the King Island emu may be an example of insular dwarfism. The King Island emu was the smallest of all known emus and had darker plumage than the mainland emu. It was black and brown and had naked blue skin on the neck, and its chicks were striped like those on the mainland. The subspecies was distinct from the likewise small and extinct Kangaroo Island emu (D. n. baudinianus) in a number of osteological details, including size. The behaviour of the King Island emu probably did not differ much from that of the mainland emu. The birds gathered in flocks to forage and during breeding time. They fed on berries, grass and seaweed. They ran swiftly and could defend themselves by kicking. The nest was shallow and consisted of dead leaves and moss. Seven to nine eggs were laid, which were incubated by both parents. Europeans discovered the King Island emu in 1802 during early expeditions to the island, and most of what is known about the bird in life comes from an interview French naturalist François Péron conducted with a sealer there, as well as depictions by artist Charles Alexandre Lesueur. They had arrived on King Island in 1802 with Nicolas Baudin's expedition, and in 1804 several live and stuffed King and Kangaroo Island emus were sent to France. The two live King Island specimens were kept in the Jardin des Plantes, and the remains of these and the other birds are scattered throughout various museums in Europe today. The logbooks of the expedition did not specify from which island each captured bird originated, or even that they were taxonomically distinct, so their status remained unclear until more than a century later. Hunting pressure and fires started by early settlers on King Island likely drove the wild population to extinction by 1805. The captive specimens in Paris both died in 1822 and are believed to have been the last of their kind. (Full article...)

    Adult and juvenile specimens, Muséum national d'Histoire naturelle, Paris; the juvenile could possibly also be a Kangaroo Island emu

    The King Island emu (Dromaius novaehollandiae minor) is an extinct subspecies of emu that was endemic to King Island, in the Bass Strait between mainland Australia and Tasmania. Its closest relative may be the also extinct Tasmanian emu (D. n. diemenensis), as they belonged to a single population until less than 14,000 years ago, when Tasmania and King Island were still connected. The small size of the King Island emu may be an example of insular dwarfism. The King Island emu was the smallest of all known emus and had darker plumage than the mainland emu. It was black and brown and had naked blue skin on the neck, and its chicks were striped like those on the mainland. The subspecies was distinct from the likewise small and extinct Kangaroo Island emu (D. n. baudinianus) in a number of osteological details, including size. The behaviour of the King Island emu probably did not differ much from that of the mainland emu. The birds gathered in flocks to forage and during breeding time. They fed on berries, grass and seaweed. They ran swiftly and could defend themselves by kicking. The nest was shallow and consisted of dead leaves and moss. Seven to nine eggs were laid, which were incubated by both parents.

    Europeans discovered the King Island emu in 1802 during early expeditions to the island, and most of what is known about the bird in life comes from an interview French naturalist François Péron conducted with a sealer there, as well as depictions by artist Charles Alexandre Lesueur. They had arrived on King Island in 1802 with Nicolas Baudin's expedition, and in 1804 several live and stuffed King and Kangaroo Island emus were sent to France. The two live King Island specimens were kept in the Jardin des Plantes, and the remains of these and the other birds are scattered throughout various museums in Europe today. The logbooks of the expedition did not specify from which island each captured bird originated, or even that they were taxonomically distinct, so their status remained unclear until more than a century later. Hunting pressure and fires started by early settlers on King Island likely drove the wild population to extinction by 1805. The captive specimens in Paris both died in 1822 and are believed to have been the last of their kind. (Full article...)
  • Image 13 An 1893 illustration of the species by John Gerrard Keulemans The white-headed fruit dove (Ptilinopus eugeniae) is a species of bird in the pigeon family Columbidae. It was described by the English ornithologist John Gould in 1856, and the specific name eugeniae honours the French empress Eugénie de Montijo. Adults of the species have white heads, a purplish-red breast patch, a grey shoulder patch, olive-green upperparts, greenish underparts with a blue tinge, and a yellowish vent. Juveniles have green heads with the white restricted to the forehead and upper throat, a much smaller grey shoulder patch, and the red breast patch restricted to the centre of the breast. The species is endemic to Makira and the nearby islands of Ugi and Malaupaina in the Solomon Islands. It inhabits lowland, hill, and ridge forest, along with neighbouring agricultural areas, and is especially common in foothills. Its diet consists of small-seeded fruits and berries. The International Union for Conservation of Nature considers it near-threatened. Although it can adapt to disturbed habitat, it is threatened by deforestation and habitat loss. (Full article...)

    An 1893 illustration of the species by John Gerrard Keulemans

    The white-headed fruit dove (Ptilinopus eugeniae) is a species of bird in the pigeon family Columbidae. It was described by the English ornithologist John Gould in 1856, and the specific name eugeniae honours the French empress Eugénie de Montijo. Adults of the species have white heads, a purplish-red breast patch, a grey shoulder patch, olive-green upperparts, greenish underparts with a blue tinge, and a yellowish vent. Juveniles have green heads with the white restricted to the forehead and upper throat, a much smaller grey shoulder patch, and the red breast patch restricted to the centre of the breast.

    The species is endemic to Makira and the nearby islands of Ugi and Malaupaina in the Solomon Islands. It inhabits lowland, hill, and ridge forest, along with neighbouring agricultural areas, and is especially common in foothills. Its diet consists of small-seeded fruits and berries. The International Union for Conservation of Nature considers it near-threatened. Although it can adapt to disturbed habitat, it is threatened by deforestation and habitat loss. (Full article...)
  • Image 14 Title page of volume 1 A History of the Birds of Europe, Including all the Species Inhabiting the Western Palearctic Region is a nine-volume ornithological book published in parts between 1871 and 1896. It was mainly written by Henry Eeles Dresser, although Richard Bowdler Sharpe co-authored the earlier volumes. It describes all the bird species reliably recorded in the wild in Europe and adjacent geographical areas with similar fauna, giving their worldwide distribution, variations in appearance and migratory movements. The pioneering ornithological work of John Ray and Francis Willughby in the seventeenth century had introduced an effective classification system based on anatomical features, and a dichotomous key to help readers identify birds. This was followed by other English-language ornithologies, notably John Gould's five-volume Birds of Europe published between 1832 and 1837. Sharpe, then librarian of the Zoological Society of London, had worked closely with Gould and wanted to expand on his work by including all species reliably recorded in Europe, North Africa, parts of the Middle East and the Atlantic archipelagos of Madeira, the Canary Islands and the Azores. He lacked the resources to undertake this task on his own, so he proposed to Dresser that they work together on this encyclopaedia, using Dresser's extensive collection of birds and their eggs and network of contacts. The Birds of Europe was published as 84 quarto parts, each typically containing 56 pages of text and eight plates of illustrations, the latter mainly by the Dutch artist John Gerrard Keulemans, and bound into volumes when all the parts were published. 339 copies were made, at a cost to each subscriber of £52 10s. Sharpe did not contribute after part 13, and was not listed as an author after part 17. Birds of Europe was well received by its contemporary reviewers, although a commentator in 2018 considered that Dresser's outdated views and the cost of his books meant that in the long run his works had limited influence. The Birds of Europe continued a tradition dating from the seventeenth century whereby the study and classification of specimens operated largely independently of those field observers who studied behaviour and ecology, a rift that continued until the 1920s, when the German naturalist Erwin Stresemann integrated the two strands as part of modern zoology. (Full article...)

    Title page of volume 1

    A History of the Birds of Europe, Including all the Species Inhabiting the Western Palearctic Region is a nine-volume ornithological book published in parts between 1871 and 1896. It was mainly written by Henry Eeles Dresser, although Richard Bowdler Sharpe co-authored the earlier volumes. It describes all the bird species reliably recorded in the wild in Europe and adjacent geographical areas with similar fauna, giving their worldwide distribution, variations in appearance and migratory movements.

    The pioneering ornithological work of John Ray and Francis Willughby in the seventeenth century had introduced an effective classification system based on anatomical features, and a dichotomous key to help readers identify birds. This was followed by other English-language ornithologies, notably John Gould's five-volume Birds of Europe published between 1832 and 1837. Sharpe, then librarian of the Zoological Society of London, had worked closely with Gould and wanted to expand on his work by including all species reliably recorded in Europe, North Africa, parts of the Middle East and the Atlantic archipelagos of Madeira, the Canary Islands and the Azores. He lacked the resources to undertake this task on his own, so he proposed to Dresser that they work together on this encyclopaedia, using Dresser's extensive collection of birds and their eggs and network of contacts.

    The Birds of Europe was published as 84 quarto parts, each typically containing 56 pages of text and eight plates of illustrations, the latter mainly by the Dutch artist John Gerrard Keulemans, and bound into volumes when all the parts were published. 339 copies were made, at a cost to each subscriber of £52 10s. Sharpe did not contribute after part 13, and was not listed as an author after part 17. Birds of Europe was well received by its contemporary reviewers, although a commentator in 2018 considered that Dresser's outdated views and the cost of his books meant that in the long run his works had limited influence. The Birds of Europe continued a tradition dating from the seventeenth century whereby the study and classification of specimens operated largely independently of those field observers who studied behaviour and ecology, a rift that continued until the 1920s, when the German naturalist Erwin Stresemann integrated the two strands as part of modern zoology. (Full article...)
  • Image 15 In the Glen Davis, New South Wales, Australia. The willie wagtail (also spelt willy wagtail), scientific name Rhipidura leucophrys, is a passerine bird native to Australia, New Guinea, the Solomon Islands, the Bismarck Archipelago, and Eastern Indonesia. It is a common and familiar bird throughout much of its range, living in most habitats apart from thick forest. Measuring 19–21.5 cm (7+1⁄2–8+1⁄2 in) in length, the willie wagtail is contrastingly coloured with almost entirely black upperparts and white underparts; the male and female have similar plumage. Three subspecies are recognised; Rhipidura leucophrys leucophrys from central and southern Australia, the smaller R. l. picata from northern Australia, and the larger R. l. melaleuca from New Guinea and islands in its vicinity. It is unrelated to the true wagtails of the genus Motacilla; it is a member of the fantail genus Rhipidura and is a part of a "core corvine" group that includes true crows and ravens, drongos and birds of paradise. Within this group, fantails are placed either in the family Dicruridae, alongside drongos, or in their own small family, Rhipiduridae. The willie wagtail is insectivorous and spends much time chasing prey in open habitat. Its common name is derived from its habit of wagging its tail horizontally when foraging on the ground. Aggressive and territorial, the willie wagtail will often harass much larger birds such as the laughing kookaburra and wedge-tailed eagle. It has responded well to human alteration of the landscape and is a common sight in urban lawns, parks, and gardens. It is widely featured in Aboriginal folklore around Australia and New Guinea in a variety of roles, from stealer of secrets and liar to a good omen for successful crops. (Full article...)

    In the Glen Davis, New South Wales, Australia.

    The willie wagtail (also spelt willy wagtail), scientific name Rhipidura leucophrys, is a passerine bird native to Australia, New Guinea, the Solomon Islands, the Bismarck Archipelago, and Eastern Indonesia. It is a common and familiar bird throughout much of its range, living in most habitats apart from thick forest. Measuring 19–21.5 cm (7+1⁄2–8+1⁄2 in) in length, the willie wagtail is contrastingly coloured with almost entirely black upperparts and white underparts; the male and female have similar plumage.

    Three subspecies are recognised; Rhipidura leucophrys leucophrys from central and southern Australia, the smaller R. l. picata from northern Australia, and the larger R. l. melaleuca from New Guinea and islands in its vicinity. It is unrelated to the true wagtails of the genus Motacilla; it is a member of the fantail genus Rhipidura and is a part of a "core corvine" group that includes true crows and ravens, drongos and birds of paradise. Within this group, fantails are placed either in the family Dicruridae, alongside drongos, or in their own small family, Rhipiduridae.

    The willie wagtail is insectivorous and spends much time chasing prey in open habitat. Its common name is derived from its habit of wagging its tail horizontally when foraging on the ground. Aggressive and territorial, the willie wagtail will often harass much larger birds such as the laughing kookaburra and wedge-tailed eagle. It has responded well to human alteration of the landscape and is a common sight in urban lawns, parks, and gardens. It is widely featured in Aboriginal folklore around Australia and New Guinea in a variety of roles, from stealer of secrets and liar to a good omen for successful crops. (Full article...)
  • Image 16 Hooded pitta in southern Thailand Pittas are a family, Pittidae, of passerine birds found in Asia, Australasia and Africa. There are 44 species of pittas, all similar in general appearance and habits. The pittas are Old World suboscines, and their closest relatives among other birds are in the genera Smithornis and Calyptomena. Initially placed in a single genus, as of 2009 they have been split into three genera: Pitta, Erythropitta and Hydrornis. Pittas are medium-sized by passerine standards, at 15 to 25 cm (5.9–9.8 in) in length, and stocky, with strong, longish legs and long feet. They have very short tails and stout, slightly decurved bills. Many have brightly coloured plumage. Most pitta species are tropical; a few species can be found in temperate climates. They are mostly found in forests, but some live in scrub and mangroves. They are highly terrestrial and mostly solitary, and usually forage on wet forest floors in areas with good ground cover. They eat earthworms, snails, insects and similar invertebrate prey, as well as small vertebrates. Pittas are monogamous and females lay up to six eggs in a large domed nest in a tree or shrub, or sometimes on the ground. Both parents care for the young. Four species of pittas are fully migratory, and several more are partially so, though their migrations are poorly understood. Four species of pitta are listed as endangered by the International Union for Conservation of Nature; a further nine species are listed as vulnerable and several more are near-threatened. The main threat to pittas is habitat loss in the form of rapid deforestation, but they are also targeted by the cage-bird trade. They are popular with birdwatchers because of their bright plumage and the difficulty in seeing them. (Full article...)

    Hooded pitta in southern Thailand

    Pittas are a family, Pittidae, of passerine birds found in Asia, Australasia and Africa. There are 44 species of pittas, all similar in general appearance and habits. The pittas are Old World suboscines, and their closest relatives among other birds are in the genera Smithornis and Calyptomena. Initially placed in a single genus, as of 2009 they have been split into three genera: Pitta, Erythropitta and Hydrornis. Pittas are medium-sized by passerine standards, at 15 to 25 cm (5.9–9.8 in) in length, and stocky, with strong, longish legs and long feet. They have very short tails and stout, slightly decurved bills. Many have brightly coloured plumage.

    Most pitta species are tropical; a few species can be found in temperate climates. They are mostly found in forests, but some live in scrub and mangroves. They are highly terrestrial and mostly solitary, and usually forage on wet forest floors in areas with good ground cover. They eat earthworms, snails, insects and similar invertebrate prey, as well as small vertebrates. Pittas are monogamous and females lay up to six eggs in a large domed nest in a tree or shrub, or sometimes on the ground. Both parents care for the young. Four species of pittas are fully migratory, and several more are partially so, though their migrations are poorly understood.

    Four species of pitta are listed as endangered by the International Union for Conservation of Nature; a further nine species are listed as vulnerable and several more are near-threatened. The main threat to pittas is habitat loss in the form of rapid deforestation, but they are also targeted by the cage-bird trade. They are popular with birdwatchers because of their bright plumage and the difficulty in seeing them. (Full article...)
  • Image 17 View from south-west Abberton Reservoir is a pumped storage freshwater reservoir in eastern England near the Essex coast, with an area of 700 hectares (1,700 acres). Most of its water is pumped from the River Stour. It is the largest body of freshwater in Essex. Constructed between 1935 and 1939, Abberton Reservoir is owned and managed by Essex and Suffolk Water, part of Northumbrian Water Group, and lies 6 km (3.7 mi) south-west of Colchester near the village of Layer de la Haye. In World War II, the reservoir was mined to deter invading seaplanes, and it was used by the RAF's No. 617 Squadron ("The Dam Busters") for practice runs for the bombing of the German dams in the Ruhr. A project to increase the capacity of Abberton Reservoir to 41,000 megalitres (9.0×109 imp gal) by raising its bank height was completed in 2013, along with a new link to transfer water from Norfolk's River Ouse to the Stour. The reservoir is important for its breeding cormorants, wintering and moulting waterfowl, and migrating birds. It is an internationally important wetland, designated as a Ramsar site, Site of Special Scientific Interest and Special Protection Area, and is listed in A Nature Conservation Review. A small part of the site is managed by the Essex Wildlife Trust. (Full article...)

    View from south-west

    Abberton Reservoir is a pumped storage freshwater reservoir in eastern England near the Essex coast, with an area of 700 hectares (1,700 acres). Most of its water is pumped from the River Stour. It is the largest body of freshwater in Essex.

    Constructed between 1935 and 1939, Abberton Reservoir is owned and managed by Essex and Suffolk Water, part of Northumbrian Water Group, and lies 6 km (3.7 mi) south-west of Colchester near the village of Layer de la Haye. In World War II, the reservoir was mined to deter invading seaplanes, and it was used by the RAF's No. 617 Squadron ("The Dam Busters") for practice runs for the bombing of the German dams in the Ruhr. A project to increase the capacity of Abberton Reservoir to 41,000 megalitres (9.0×109 imp gal) by raising its bank height was completed in 2013, along with a new link to transfer water from Norfolk's River Ouse to the Stour.

    The reservoir is important for its breeding cormorants, wintering and moulting waterfowl, and migrating birds. It is an internationally important wetland, designated as a Ramsar site, Site of Special Scientific Interest and Special Protection Area, and is listed in A Nature Conservation Review. A small part of the site is managed by the Essex Wildlife Trust. (Full article...)
  • Image 18 Male Laysan honeycreeper photographed by Donald R. Dickey in 1923, a few days before the extinction of the species The Laysan honeycreeper (Himatione fraithii), also known as the Laysan ʻapapane or Laysan honeyeater, is an extinct species of finch that was endemic to the island of Laysan in the Northwestern Hawaiian Islands. The bird was first recorded in 1828 and in 1892 received its scientific name from Walter Rothschild, who placed it in the genus Himatione along with the ʻapapane. The specific name, fraithii, refers to George D. Freeth, the self-appointed governor of Laysan, but was misspelled. Rothschild attempted to emend it to freethi in a later publication. This was accepted by most subsequent authors throughout the 20th century, and the bird was also considered a subspecies of the ʻapapane, as H. sanguinea freethii, for most of this time. By the 21st century, after further research, the original name was reinstated and it was considered a full species again. As a Hawaiian honeycreeper, a grouping within the finch subfamily Carduelinae, its ancestors are thought to have come from Asia. The Laysan honeycreeper was 13–15 cm (5–6 in) long and its wing measured 64–69 mm (2.5–2.7 in). It was bright scarlet vermilion with a faint tint of golden orange on the head, breast and upper abdomen; the rest of its upper parts were orange scarlet. The lower abdomen was dusky gray that faded into brownish white, and the undertail covert feathers were grayish. The wings, tail, bill, and legs were dark brown, and the iris was black with a brown outline. Immature birds were brown with paler lower parts, and had green edges to their wing-covert feathers. The bill was slender and downturned. The sexes were alike, though the bill, wings, and tail were slightly shorter in the female. The ʻapapane differs from the Laysan honeycreeper in features such as being blood-red overall and having a longer bill. The song of the Laysan honeycreeper was described as low and sweet, consisting of several notes. Laysan is a remote coral island with an area of 3.6 km2 (1.4 sq mi). The honeycreeper lived throughout, but was most abundant in the interior among tall grass and low bushes near the open plain that bordered the island's lagoon. This bird was very active and, though less trusting than other birds, sometimes entered buildings to hunt moths and for roosting at night. It was nectarivorous and insectivorous and, unlike the ʻapapane, also foraged on the ground. It gathered nectar and insects from flowers, such as caterpillars and moths called millers, only eating the soft parts of the latter. The nest was made of fine grass and rootlets with some dry grass. The breeding season was probably between January and June, and the clutch size was four or five eggs. The eggs were glossless white, with blotches and spots at the larger end. A typical egg measured 18 by 13.7 mm (0.71 by 0.54 in). The bird did not seem to be abundant when discovered and was considered the rarest of the island's birds. In 1903, domestic rabbits were introduced to the island and proceeded to destroy its vegetation. By the visit of the Tanager Expedition in 1923, Laysan had become barren and desert-like, and only three Laysan honeycreepers were found, one of which was filmed. A few days later, on April 23, a sandstorm hit the island, and the last birds perished due to lack of cover. The destruction of Laysan's vegetation led to the extinction of three out of five of its endemic land birds. (Full article...)

    Male Laysan honeycreeper photographed by Donald R. Dickey in 1923, a few days before the extinction of the species

    The Laysan honeycreeper (Himatione fraithii), also known as the Laysan ʻapapane or Laysan honeyeater, is an extinct species of finch that was endemic to the island of Laysan in the Northwestern Hawaiian Islands. The bird was first recorded in 1828 and in 1892 received its scientific name from Walter Rothschild, who placed it in the genus Himatione along with the ʻapapane. The specific name, fraithii, refers to George D. Freeth, the self-appointed governor of Laysan, but was misspelled. Rothschild attempted to emend it to freethi in a later publication. This was accepted by most subsequent authors throughout the 20th century, and the bird was also considered a subspecies of the ʻapapane, as H. sanguinea freethii, for most of this time. By the 21st century, after further research, the original name was reinstated and it was considered a full species again. As a Hawaiian honeycreeper, a grouping within the finch subfamily Carduelinae, its ancestors are thought to have come from Asia.

    The Laysan honeycreeper was 13–15 cm (5–6 in) long and its wing measured 64–69 mm (2.5–2.7 in). It was bright scarlet vermilion with a faint tint of golden orange on the head, breast and upper abdomen; the rest of its upper parts were orange scarlet. The lower abdomen was dusky gray that faded into brownish white, and the undertail covert feathers were grayish. The wings, tail, bill, and legs were dark brown, and the iris was black with a brown outline. Immature birds were brown with paler lower parts, and had green edges to their wing-covert feathers. The bill was slender and downturned. The sexes were alike, though the bill, wings, and tail were slightly shorter in the female. The ʻapapane differs from the Laysan honeycreeper in features such as being blood-red overall and having a longer bill. The song of the Laysan honeycreeper was described as low and sweet, consisting of several notes. Laysan is a remote coral island with an area of 3.6 km2 (1.4 sq mi). The honeycreeper lived throughout, but was most abundant in the interior among tall grass and low bushes near the open plain that bordered the island's lagoon.

    This bird was very active and, though less trusting than other birds, sometimes entered buildings to hunt moths and for roosting at night. It was nectarivorous and insectivorous and, unlike the ʻapapane, also foraged on the ground. It gathered nectar and insects from flowers, such as caterpillars and moths called millers, only eating the soft parts of the latter. The nest was made of fine grass and rootlets with some dry grass. The breeding season was probably between January and June, and the clutch size was four or five eggs. The eggs were glossless white, with blotches and spots at the larger end. A typical egg measured 18 by 13.7 mm (0.71 by 0.54 in). The bird did not seem to be abundant when discovered and was considered the rarest of the island's birds. In 1903, domestic rabbits were introduced to the island and proceeded to destroy its vegetation. By the visit of the Tanager Expedition in 1923, Laysan had become barren and desert-like, and only three Laysan honeycreepers were found, one of which was filmed. A few days later, on April 23, a sandstorm hit the island, and the last birds perished due to lack of cover. The destruction of Laysan's vegetation led to the extinction of three out of five of its endemic land birds. (Full article...)
  • Image 19 At Little Tobago Island, Trinidad, and Tobago The red-billed tropicbird (Phaethon aethereus) is a tropicbird, one of three closely related species of seabird of tropical oceans. Superficially resembling a tern in appearance, it has mostly white plumage with some black markings on the wings and back, a black mask and, as its common name suggests, a red bill. Most adults have tail streamers that are about two times their body length, with those in males being generally longer than those in females. The red-billed tropicbird itself has three subspecies recognized, including the nominate. The subspecies mesonauta is distinguished from the nominate by the rosy tinge of its fresh plumage, and the subspecies indicus can be differentiated by its smaller size, more restricted mask, and more orange bill. This species ranges across the tropical Atlantic, eastern Pacific, and Indian Oceans. The nominate is found in the southern Atlantic Ocean, the subspecies indicus in the waters off of the Middle East and in the Indian Ocean, and the subspecies mesonauta in the eastern portions of both the Atlantic and the Pacific Oceans and in the Caribbean. It was one of the many species described by Carl Linnaeus in his 1758 10th edition of Systema Naturae. Nesting takes place in loose colonies, as they nest a scrape found on a cliff face that is easy to take off from. A single egg is laid and is incubated by both sexes for about six weeks. Whether the egg hatches or not can be influenced by pollution and weather, although the latter has a minimal effect on whether a chick fledges or not. After a chick fledges, the parents will usually stop visiting the nest and the chick will leave. Birds of all ages feed on fish and squid, catching them by diving from the air into the water. However, the red-billed tropicbird sometimes follows surface-feeding predators. The predators will drive the prey to the surface, which are then seized by the tropicbird. In some areas, introduced black and brown rats raid nests for eggs and young. Cats also threaten the red-billed tropicbird. This bird is considered to be a least-concern species according to the International Union for Conservation of Nature (IUCN), though populations are thought to be declining. In some places, such as Brazil and Mexico, this bird is considered to be threatened. (Full article...)

    At Little Tobago Island, Trinidad, and Tobago

    The red-billed tropicbird (Phaethon aethereus) is a tropicbird, one of three closely related species of seabird of tropical oceans. Superficially resembling a tern in appearance, it has mostly white plumage with some black markings on the wings and back, a black mask and, as its common name suggests, a red bill. Most adults have tail streamers that are about two times their body length, with those in males being generally longer than those in females. The red-billed tropicbird itself has three subspecies recognized, including the nominate. The subspecies mesonauta is distinguished from the nominate by the rosy tinge of its fresh plumage, and the subspecies indicus can be differentiated by its smaller size, more restricted mask, and more orange bill. This species ranges across the tropical Atlantic, eastern Pacific, and Indian Oceans. The nominate is found in the southern Atlantic Ocean, the subspecies indicus in the waters off of the Middle East and in the Indian Ocean, and the subspecies mesonauta in the eastern portions of both the Atlantic and the Pacific Oceans and in the Caribbean. It was one of the many species described by Carl Linnaeus in his 1758 10th edition of Systema Naturae.

    Nesting takes place in loose colonies, as they nest a scrape found on a cliff face that is easy to take off from. A single egg is laid and is incubated by both sexes for about six weeks. Whether the egg hatches or not can be influenced by pollution and weather, although the latter has a minimal effect on whether a chick fledges or not. After a chick fledges, the parents will usually stop visiting the nest and the chick will leave. Birds of all ages feed on fish and squid, catching them by diving from the air into the water. However, the red-billed tropicbird sometimes follows surface-feeding predators. The predators will drive the prey to the surface, which are then seized by the tropicbird.

    In some areas, introduced black and brown rats raid nests for eggs and young. Cats also threaten the red-billed tropicbird. This bird is considered to be a least-concern species according to the International Union for Conservation of Nature (IUCN), though populations are thought to be declining. In some places, such as Brazil and Mexico, this bird is considered to be threatened. (Full article...)
  • Image 20 Black currawong, Tasmania The black currawong (Strepera fuliginosa), also known locally as the black jay, is a large passerine bird endemic to Tasmania and the nearby islands within the Bass Strait. One of three currawong species in the genus Strepera, it is closely related to the butcherbirds and Australian magpie within the family Artamidae. It is a large crow-like bird, around 50 cm (20 in) long on average, with yellow irises, a heavy bill, and black plumage with white wing patches. The male and female are similar in appearance. Three subspecies are recognised, one of which, Strepera fuliginosa colei of King Island, is vulnerable to extinction. Within its range, the black currawong is generally sedentary, although populations at higher altitudes relocate to lower areas during the cooler months. The habitat includes densely forested areas as well as alpine heathland. It is rare below altitudes of 200 m (660 ft). Omnivorous, its diet includes a variety of berries, invertebrates, and small vertebrates. Less arboreal than the pied currawong, the black currawong spends more time foraging on the ground. It roosts and breeds in trees. (Full article...)

    Black currawong, Tasmania

    The black currawong (Strepera fuliginosa), also known locally as the black jay, is a large passerine bird endemic to Tasmania and the nearby islands within the Bass Strait. One of three currawong species in the genus Strepera, it is closely related to the butcherbirds and Australian magpie within the family Artamidae. It is a large crow-like bird, around 50 cm (20 in) long on average, with yellow irises, a heavy bill, and black plumage with white wing patches. The male and female are similar in appearance. Three subspecies are recognised, one of which, Strepera fuliginosa colei of King Island, is vulnerable to extinction.

    Within its range, the black currawong is generally sedentary, although populations at higher altitudes relocate to lower areas during the cooler months. The habitat includes densely forested areas as well as alpine heathland. It is rare below altitudes of 200 m (660 ft). Omnivorous, its diet includes a variety of berries, invertebrates, and small vertebrates. Less arboreal than the pied currawong, the black currawong spends more time foraging on the ground. It roosts and breeds in trees. (Full article...)

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Male common teal producing feeding traces on a River Tyne mudflat.

Bird ichnology is the study of avian life traces in ornithology and paleontology. Such life traces can include footprints, nests, feces and coproliths. Scientists gain insight about the behavior and diversity of birds by studying such evidence.

Ichnofossils (or ichnites) are especially important for clarifying the evolution and prehistoric diversity of taxa. These cannot usually be associated with a particular genus, let alone species of bird, as hardly ever they are associated with fossil bones. But it is possible to group them into ichnotaxa based on their morphology (form). In practice, the details of shape that reveal the birds' behavior or biologic affinity are generally given more weight in ichnologic classification. (Full article...)

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Crested treeswift (H. coronata)

Treeswifts or crested swifts are a family, the Hemiprocnidae, of aerial near passerine birds, closely related to the true swifts. The family contains a single genus, Hemiprocne, with four species. They are distributed from India and Southeast Asia through Indonesia to New Guinea and the Solomon Islands.

Treeswifts are small to medium-sized swifts, ranging in length from 15 to 30 cm. They have long wings, with most of the length coming from the length of the primaries; their arms are actually quite short. They visibly differ from the other swifts in matters of plumage, which is softer, and they have crests or other facial ornaments, and long, forked tails. Anatomically they are separated from the true swifts by skeletal details in the cranium and palate, the anatomy of the tarsus, and a nonreversible hind toe that is used for perching on branches (an activity in which true swifts are unable to engage). The males have iridescent mantle plumage. They also have diastataxic wings, that is they lack a fifth secondary feather unlike swifts in the Apodini, which are eutaxic. The treeswifts exhibit a wide range of habitat preferences. One species, the whiskered treeswift, is a species belonging to primary forest. Highly manoeuvrable, it feeds close to vegetation beneath the canopy, and only rarely ventures into secondary forests or plantations, but never over open ground. Other species are less restricted; the crested treeswift makes use of a range of habitats including humid forests and deciduous woodland, and the grey-rumped treeswift occupies almost every habitat type available from the mangrove forests to hill forests. All species feed on insects, although exact details of what prey are taken has not been studied in detail. (Full article...)

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Anatomy:   Anatomy • Skeleton • Flight • Eggs • Feathers • Plumage

Evolution and extinction:   Evolution • Archaeopteryx • Hybridisation • Late Quaternary prehistoric birds • Fossils • Taxonomy • Extinction

Behaviour:   Singing • Intelligence • Migration • Reproduction • Nesting • Incubation • Brood parasites

Bird orders:   Struthioniformes • Tinamiformes • Anseriformes • Accipitriformes • Galliformes • Gaviiformes • Podicipediformes • Procellariiformes • Sphenisciformes • Pelecaniformes • Ciconiiformes • Phoenicopteriformes • Falconiformes • Gruiformes • Charadriiformes • Pteroclidiformes • Columbiformes • Psittaciformes • Cuculiformes • Strigiformes • Caprimulgiformes • Apodiformes • Coraciiformes • Piciformes • Trogoniformes • Coliiformes • Passeriformes

Bird lists:   Families and orders • Lists by region

Birds and humans:   Ringing • Ornithology • Bird collections • Birdwatching • Birdfeeding • Conservation • Aviculture

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There is also Birds of North America, Cornell University's massive project collecting information on every breeding bird in the ABA area. It is available for US$40 a year.

For more sources, including printed sources, see WikiProject Birds.

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The nidopallium, meaning nested pallium, is the region of the avian brain that is used mostly for some types of executive functions but also for other higher cognitive tasks. The region was renamed nidopallium in 2002 during the Avian Brain Nomenclature Consortium because the prior name, neostriatum, suggested that the region was used for more primitive functions as the neostriatum in mammalian brains is sub-cortical. (Full article...)

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Male and female superb fairy-wrens
The superb fairy-wren (Malurus cyaneus), also known as superb blue-wren or colloquially as blue wren, is a passerine bird of the family Maluridae. Sedentary and territorial, it is found across southeastern Australia. The male in breeding plumage has a striking bright blue forehead, ear coverts, mantle and tail with a black mask and black or dark blue throat. Non-breeding males, females and juveniles are predominantly grey-brown in colour. Two subspecies are recognised. Like other fairy-wrens, the superb fairy-wren is notable for several peculiar behavioural characteristics; birds are socially monogamous and sexually promiscuous. Male wrens pluck yellow petals and display them to females as part of a courtship display. The superb fairy-wren can be found in almost any area that has at least a little dense undergrowth for shelter. It has adapted well to the urban environment. The superb fairy-wren mainly eats insects and supplements its diet with seeds.


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Sources

  1. ^ Woods, R.L. (1967). The Modern Handbook of Humor. McGraw-Hill. p. 30. Retrieved February 7, 2020.
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