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The Birds Portal

Birds are a group of warm-blooded vertebrates constituting the class Aves (/ˈeɪviːz/), 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, more than half of which 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 recent estimates, modern birds (Neornithes) evolved in the Late Cretaceous and diversified dramatically around the time of the Cretaceous–Paleogene extinction event 66 million years ago, which killed off the pterosaurs and all non-avian dinosaurs.

Many social species preserve knowledge across generations (culture). Birds are social, communicating with visual signals, calls, and songs, and participating in such behaviours 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 perched in a honey mesquite tree The cactus wren (Campylorhynchus brunneicapillus) is a species of wren that is endemic to the deserts of the southwestern United States and northern and central Mexico. It is the state bird of Arizona, and the largest wren in the United States. Its plumage is brown, with black and white spots as markings. It has a distinctive white eyebrow that sweeps to the nape of the neck. The chest is white, whereas the underparts are cinnamon-buff colored. Both sexes appear similar. The tail, as well as flight feathers, are barred in black and white. Their song is a loud raspy chirrup; akin in the description of some ornithologists to the sound of a car engine that will not start. It is well-adapted to its native desert environment, and the birds can meet their water needs from their diet which consists chiefly of insects, but also of some plant matter. The cactus wren is a poor flier and generally forages for food on the ground. Ornithologists generally recognize seven subspecies, with the exact taxonomy under dispute. Its common name derives from their frequenting desert cactus plants such as the saguaro and cholla, building nests, roosting, and seeking protection from predators among them. Its bulky and globular nests are constructed of plant material and lined with feathers. They do not migrate; instead, they establish and defend the territories around their nests where they live all year-round. It lives in pairs, or as family groups from late spring through winter. Pairing among cactus wrens is monogamous; in each breeding season, the males chiefly build nests, the females incubate eggs, and both parents feed the young. Populations have declined as the species faces threats related to human activities and habitat loss, although the species remains abundant. Habitat fragmentation and fire have been of particular concern, as the cactus wren is slow to disperse into new habitats. Introduced species have also hurt populations. Feral cats hunt many birds in urban settings, and invasive grasses take up valuable foraging space, reducing habitat size. Despite these threats, the cactus wren has proved adaptable. Cactus wrens have learned to coexist with humans effectively, using human materials and structures for nesting, and even learning to take insects from vehicle radiator grilles. The population still numbers in the millions, leading the International Union for Conservation of Nature to consider the cactus wren a species of least concern. (Full article...)

    Adult perched in a honey mesquite tree

    The cactus wren (Campylorhynchus brunneicapillus) is a species of wren that is endemic to the deserts of the southwestern United States and northern and central Mexico. It is the state bird of Arizona, and the largest wren in the United States. Its plumage is brown, with black and white spots as markings. It has a distinctive white eyebrow that sweeps to the nape of the neck. The chest is white, whereas the underparts are cinnamon-buff colored. Both sexes appear similar. The tail, as well as flight feathers, are barred in black and white. Their song is a loud raspy chirrup; akin in the description of some ornithologists to the sound of a car engine that will not start. It is well-adapted to its native desert environment, and the birds can meet their water needs from their diet which consists chiefly of insects, but also of some plant matter. The cactus wren is a poor flier and generally forages for food on the ground. Ornithologists generally recognize seven subspecies, with the exact taxonomy under dispute.

    Its common name derives from their frequenting desert cactus plants such as the saguaro and cholla, building nests, roosting, and seeking protection from predators among them. Its bulky and globular nests are constructed of plant material and lined with feathers. They do not migrate; instead, they establish and defend the territories around their nests where they live all year-round. It lives in pairs, or as family groups from late spring through winter. Pairing among cactus wrens is monogamous; in each breeding season, the males chiefly build nests, the females incubate eggs, and both parents feed the young.

    Populations have declined as the species faces threats related to human activities and habitat loss, although the species remains abundant. Habitat fragmentation and fire have been of particular concern, as the cactus wren is slow to disperse into new habitats. Introduced species have also hurt populations. Feral cats hunt many birds in urban settings, and invasive grasses take up valuable foraging space, reducing habitat size. Despite these threats, the cactus wren has proved adaptable. Cactus wrens have learned to coexist with humans effectively, using human materials and structures for nesting, and even learning to take insects from vehicle radiator grilles. The population still numbers in the millions, leading the International Union for Conservation of Nature to consider the cactus wren a species of least concern. (Full article...)
  • Image 2 in the Maasai Mara The secretarybird or secretary bird (Sagittarius serpentarius) is a large bird of prey that is endemic to Africa. It is mostly terrestrial, spending most of its time on the ground, and is usually found in the open grasslands and savanna of the sub-Saharan region. John Frederick Miller described the species in 1779. A member of the order Accipitriformes, which also includes many other diurnal birds of prey such as eagles, hawks, kites, vultures, and harriers, it is placed in its own family, Sagittariidae. The secretarybird is instantly recognizable as a very large bird with an eagle-like body on crane-like legs that give the bird a height of as much as 1.3 m (4 ft 3 in). The sexes are similar in appearance. Adults have a featherless red-orange face and predominantly grey plumage, with a flattened dark crest and black flight feathers and thighs. Breeding can take place at any time of year but tends to be late in the dry season. The nest is built at the top of a thorny tree, and a clutch of one to three eggs is laid. In years with plentiful food all three young can survive to fledging. The secretarybird hunts and catches prey on the ground, often stomping on victims to kill them. Insects and small vertebrates make up its diet. (Full article...)

    in the Maasai Mara

    The secretarybird or secretary bird (Sagittarius serpentarius) is a large bird of prey that is endemic to Africa. It is mostly terrestrial, spending most of its time on the ground, and is usually found in the open grasslands and savanna of the sub-Saharan region. John Frederick Miller described the species in 1779. A member of the order Accipitriformes, which also includes many other diurnal birds of prey such as eagles, hawks, kites, vultures, and harriers, it is placed in its own family, Sagittariidae.

    The secretarybird is instantly recognizable as a very large bird with an eagle-like body on crane-like legs that give the bird a height of as much as 1.3 m (4 ft 3 in). The sexes are similar in appearance. Adults have a featherless red-orange face and predominantly grey plumage, with a flattened dark crest and black flight feathers and thighs.

    Breeding can take place at any time of year but tends to be late in the dry season. The nest is built at the top of a thorny tree, and a clutch of one to three eggs is laid. In years with plentiful food all three young can survive to fledging. The secretarybird hunts and catches prey on the ground, often stomping on victims to kill them. Insects and small vertebrates make up its diet. (Full article...)
  • Image 3 Illustration from 1861 Ibis article. The African river martin (Pseudochelidon eurystomina) is a passerine bird, one of two members of the river martin subfamily of the swallow family, Hirundinidae. When discovered, it was not initially recognised as a swallow, and its structural differences from most of its relatives, including its stout bill and robust legs and feet, have led to its current placement in a separate subfamily shared only with the Asian white-eyed river martin. The African river martin is a large swallow, mainly black with a blue-green gloss to the head and a greener tint to the back and wings. The under-wings are brownish, the underparts are purple-black, and the flight feathers are black. This martin has red eyes, a broad orange-red bill and a black, square tail. Young birds are similar in appearance to the adults, but have browner plumage. This species has a variety of unmusical calls, and displays both in flight and on the ground, although the purpose of the terrestrial display is unknown. The main breeding areas are in the Democratic Republic of the Congo (DRC) along the Congo River and its tributary, the Ubangi, in habitats characterised by a mixture of tropical forest types including swampy or seasonally flooded woodland. The African river martin is migratory, wintering in coastal savanna in southern Gabon and the Republic of the Congo. Breeding also occurs in these coastal areas, but it is unknown whether the migrants are raising a second brood or if there is a separate resident population. This martin feeds in flocks throughout the year, catching a variety of insects in the air, especially flying ants. It does not use perches during the breeding season, although it will often land on the ground. The African river martin nests in burrows in river sand banks, often alongside rosy bee-eaters, but its incubation and fledging times are not known. It also digs tunnels for night-time shelter when in its wintering areas. It appears to be common within its restricted range, despite being caught in large numbers by the local population for food, and large flocks are sometimes seen. However, due to a lack of detailed information about its breeding range and population numbers, this species is classed as Data Deficient by the International Union for Conservation of Nature (IUCN). (Full article...)

    Illustration from 1861 Ibis article.

    The African river martin (Pseudochelidon eurystomina) is a passerine bird, one of two members of the river martin subfamily of the swallow family, Hirundinidae. When discovered, it was not initially recognised as a swallow, and its structural differences from most of its relatives, including its stout bill and robust legs and feet, have led to its current placement in a separate subfamily shared only with the Asian white-eyed river martin. The African river martin is a large swallow, mainly black with a blue-green gloss to the head and a greener tint to the back and wings. The under-wings are brownish, the underparts are purple-black, and the flight feathers are black. This martin has red eyes, a broad orange-red bill and a black, square tail. Young birds are similar in appearance to the adults, but have browner plumage. This species has a variety of unmusical calls, and displays both in flight and on the ground, although the purpose of the terrestrial display is unknown.

    The main breeding areas are in the Democratic Republic of the Congo (DRC) along the Congo River and its tributary, the Ubangi, in habitats characterised by a mixture of tropical forest types including swampy or seasonally flooded woodland. The African river martin is migratory, wintering in coastal savanna in southern Gabon and the Republic of the Congo. Breeding also occurs in these coastal areas, but it is unknown whether the migrants are raising a second brood or if there is a separate resident population. This martin feeds in flocks throughout the year, catching a variety of insects in the air, especially flying ants. It does not use perches during the breeding season, although it will often land on the ground.

    The African river martin nests in burrows in river sand banks, often alongside rosy bee-eaters, but its incubation and fledging times are not known. It also digs tunnels for night-time shelter when in its wintering areas. It appears to be common within its restricted range, despite being caught in large numbers by the local population for food, and large flocks are sometimes seen. However, due to a lack of detailed information about its breeding range and population numbers, this species is classed as Data Deficient by the International Union for Conservation of Nature (IUCN). (Full article...)
  • Image 4 Pigeon with German miniature camera, probably during the First World War Pigeon photography is an aerial photography technique invented in 1907 by the German apothecary Julius Neubronner, who also used pigeons to deliver medications. A homing pigeon was fitted with an aluminium breast harness to which a lightweight time-delayed miniature camera could be attached. Neubronner's German patent application was initially rejected, but was granted in December 1908 after he produced authenticated photographs taken by his pigeons. He publicized the technique at the 1909 Dresden International Photographic Exhibition, and sold some images as postcards at the Frankfurt International Aviation Exhibition and at the 1910 and 1911 Paris Air Shows. Initially, the military potential of pigeon photography for aerial reconnaissance appeared interesting. Battlefield tests in World War I provided encouraging results, but the ancillary technology of mobile dovecotes for messenger pigeons had the greatest impact. Owing to the rapid development of aviation during the war, military interest in pigeon photography faded and Neubronner abandoned his experiments. The idea was briefly resurrected in the 1930s by a Swiss clockmaker, and reportedly also by the German and French militaries. Although war pigeons were deployed extensively during World War II, it is unclear to what extent, if any, birds were involved in aerial reconnaissance. The United States Central Intelligence Agency (CIA) later developed a battery-powered camera designed for espionage pigeon photography; details of its use remain classified. The construction of sufficiently small and light cameras with a timer mechanism, and the training and handling of the birds to carry the necessary loads, presented major challenges, as did the limited control over the pigeons' position, orientation and speed when the photographs were being taken. In 2004, the British Broadcasting Corporation (BBC) used miniature television cameras attached to falcons and goshawks to obtain live footage, and today some researchers, enthusiasts and artists similarly deploy crittercams with various species of animals. (Full article...)
    Pigeon with German miniature camera, probably during the First World War


    Pigeon photography is an aerial photography technique invented in 1907 by the German apothecary Julius Neubronner, who also used pigeons to deliver medications. A homing pigeon was fitted with an aluminium breast harness to which a lightweight time-delayed miniature camera could be attached. Neubronner's German patent application was initially rejected, but was granted in December 1908 after he produced authenticated photographs taken by his pigeons. He publicized the technique at the 1909 Dresden International Photographic Exhibition, and sold some images as postcards at the Frankfurt International Aviation Exhibition and at the 1910 and 1911 Paris Air Shows.

    Initially, the military potential of pigeon photography for aerial reconnaissance appeared interesting. Battlefield tests in World War I provided encouraging results, but the ancillary technology of mobile dovecotes for messenger pigeons had the greatest impact. Owing to the rapid development of aviation during the war, military interest in pigeon photography faded and Neubronner abandoned his experiments. The idea was briefly resurrected in the 1930s by a Swiss clockmaker, and reportedly also by the German and French militaries. Although war pigeons were deployed extensively during World War II, it is unclear to what extent, if any, birds were involved in aerial reconnaissance. The United States Central Intelligence Agency (CIA) later developed a battery-powered camera designed for espionage pigeon photography; details of its use remain classified.

    The construction of sufficiently small and light cameras with a timer mechanism, and the training and handling of the birds to carry the necessary loads, presented major challenges, as did the limited control over the pigeons' position, orientation and speed when the photographs were being taken. In 2004, the British Broadcasting Corporation (BBC) used miniature television cameras attached to falcons and goshawks to obtain live footage, and today some researchers, enthusiasts and artists similarly deploy crittercams with various species of animals. (Full article...)
  • Image 5 Subfossil bones described in 1879, including two skulls, a pelvis, and limb bones The Rodrigues rail (Erythromachus leguati), also known as Leguat's gelinote or Leguat's rail, is an extinct species of the rail family that was endemic to the Mascarene island of Rodrigues. The bird was first documented from life by two accounts from 1691–93 and 1725–26. Subfossil remains were later discovered and correlated with the old accounts in 1874, and the species was named E. leguati in Leguat's honour. It is generally kept in its own genus, Erythromachus, but has sometimes been assigned to the genus Aphanapteryx along with its close relative the red rail (A. bonasia) of Mauritius; their relationship with other rails is unclear. The Rodrigues rail was about 35 cm (14 in) long and weighed at least 500 g (18 oz). It was described as having grey plumage, a red beak, red legs, and a naked red patch around the eye. The beak was long and curved downwards. It was flightless and fed on tortoise eggs. It was described as being attracted to red objects, which humans exploited while hunting it. The Rodrigues rail is believed to have become extinct in the mid-18th century mainly because of predation by introduced cats and hunting. (Full article...)

    Subfossil bones described in 1879, including two skulls, a pelvis, and limb bones

    The Rodrigues rail (Erythromachus leguati), also known as Leguat's gelinote or Leguat's rail, is an extinct species of the rail family that was endemic to the Mascarene island of Rodrigues. The bird was first documented from life by two accounts from 1691–93 and 1725–26. Subfossil remains were later discovered and correlated with the old accounts in 1874, and the species was named E. leguati in Leguat's honour. It is generally kept in its own genus, Erythromachus, but has sometimes been assigned to the genus Aphanapteryx along with its close relative the red rail (A. bonasia) of Mauritius; their relationship with other rails is unclear.

    The Rodrigues rail was about 35 cm (14 in) long and weighed at least 500 g (18 oz). It was described as having grey plumage, a red beak, red legs, and a naked red patch around the eye. The beak was long and curved downwards. It was flightless and fed on tortoise eggs. It was described as being attracted to red objects, which humans exploited while hunting it. The Rodrigues rail is believed to have become extinct in the mid-18th century mainly because of predation by introduced cats and hunting. (Full article...)
  • Image 6 Killdeer in breeding plumage. The killdeer (Charadrius vociferus) is a large plover found in the Americas. It gets its name from its shrill, two-syllable call, which is often heard. It was described and given its current scientific name in 1758 by Carl Linnaeus in the 10th edition of his Systema Naturae. Three subspecies are described. Its upperparts are mostly brown with rufous fringes, the head has patches of white and black, and two black bands cross the breast. The belly and the rest of the breast are white. The nominate (or originally described) subspecies breeds from southeastern Alaska and southern Canada to Mexico. It is seen year-round in the southern half of its breeding range; the subspecies C. v. ternominatus is resident in the West Indies, and C. v. peruvianus inhabits Peru and surrounding South American countries throughout the year. North American breeders winter from their resident range south to Central America, the West Indies, and the northernmost portions of South America. Despite their name, they are not known for killing deer. The nonbreeding habitat of the killdeer includes coastal wetlands, beach habitats, and coastal fields. Its breeding grounds are generally open fields with short vegetation (but locations such as rooftops are sometimes used); although it is a shorebird, it does not necessarily nest close to water. The nest itself is a scrape lined with vegetation and white material, such as pebbles or seashell fragments. This bird lays a clutch of four to six buff to beige eggs with dark markings. The breeding season (starting with egg-laying) occurs from mid-March to August, with later timing of egg-laying in the northern portion of the range. Both parents incubate the eggs for 22 to 28 days typically. The young stay in the nest until the day after being hatched, when they are led by their parents to a feeding territory (generally with dense vegetation where hiding spots are abundant), where the chicks feed themselves. The young then fledge about 31 days after hatching, and breeding first occurs after one year of age. The killdeer primarily feeds on insects, although other invertebrates and seeds are eaten. It forages almost exclusively in fields, especially those with short vegetation and with cattle and standing water. It primarily forages during the day, but in the nonbreeding season, when the moon is full or close to full, it forages at night, likely because of increased insect abundance and reduced predation during the night. Predators of the killdeer include various birds and mammals. Its multiple responses to predation range from calling to the "ungulate display", which can be fatal for the performing individual. This bird is classified as least concern by the International Union for Conservation of Nature, because of its large range and population. Its population is declining, but this trend is not severe enough for the killdeer to be considered a vulnerable species. It is protected by the American Migratory Bird Treaty Act of 1918 and the Canadian Migratory Birds Convention Act. (Full article...)

    Killdeer in breeding plumage.

    The killdeer (Charadrius vociferus) is a large plover found in the Americas. It gets its name from its shrill, two-syllable call, which is often heard. It was described and given its current scientific name in 1758 by Carl Linnaeus in the 10th edition of his Systema Naturae. Three subspecies are described. Its upperparts are mostly brown with rufous fringes, the head has patches of white and black, and two black bands cross the breast. The belly and the rest of the breast are white. The nominate (or originally described) subspecies breeds from southeastern Alaska and southern Canada to Mexico. It is seen year-round in the southern half of its breeding range; the subspecies C. v. ternominatus is resident in the West Indies, and C. v. peruvianus inhabits Peru and surrounding South American countries throughout the year. North American breeders winter from their resident range south to Central America, the West Indies, and the northernmost portions of South America. Despite their name, they are not known for killing deer.

    The nonbreeding habitat of the killdeer includes coastal wetlands, beach habitats, and coastal fields. Its breeding grounds are generally open fields with short vegetation (but locations such as rooftops are sometimes used); although it is a shorebird, it does not necessarily nest close to water. The nest itself is a scrape lined with vegetation and white material, such as pebbles or seashell fragments. This bird lays a clutch of four to six buff to beige eggs with dark markings. The breeding season (starting with egg-laying) occurs from mid-March to August, with later timing of egg-laying in the northern portion of the range. Both parents incubate the eggs for 22 to 28 days typically. The young stay in the nest until the day after being hatched, when they are led by their parents to a feeding territory (generally with dense vegetation where hiding spots are abundant), where the chicks feed themselves. The young then fledge about 31 days after hatching, and breeding first occurs after one year of age.

    The killdeer primarily feeds on insects, although other invertebrates and seeds are eaten. It forages almost exclusively in fields, especially those with short vegetation and with cattle and standing water. It primarily forages during the day, but in the nonbreeding season, when the moon is full or close to full, it forages at night, likely because of increased insect abundance and reduced predation during the night. Predators of the killdeer include various birds and mammals. Its multiple responses to predation range from calling to the "ungulate display", which can be fatal for the performing individual. This bird is classified as least concern by the International Union for Conservation of Nature, because of its large range and population. Its population is declining, but this trend is not severe enough for the killdeer to be considered a vulnerable species. It is protected by the American Migratory Bird Treaty Act of 1918 and the Canadian Migratory Birds Convention Act. (Full article...)
  • Image 7 In Prospect Park, New York, USA The mourning dove (Zenaida macroura) is a member of the dove family, Columbidae. The bird is also known as the American mourning dove, the rain dove, the chueybird, colloquially as the turtle dove, and it was once known as the Carolina pigeon and Carolina turtledove. It is one of the most abundant and widespread North American birds and a popular gamebird, with more than 20 million birds (up to 70 million in some years) shot annually in the U.S., both for sport and meat. Its ability to sustain its population under such pressure is due to its prolific breeding; in warm areas, one pair may raise up to six broods of two young each in a single year. The wings make an unusual whistling sound upon take-off and landing, a form of sonation. The bird is a strong flier, capable of speeds up to 88 km/h (55 mph). Mourning doves are light gray and brown and generally muted in color. Males and females are similar in appearance. The species is generally monogamous, with two squabs (young) per brood. Both parents incubate and care for the young. Mourning doves eat almost exclusively seeds, but the young are fed crop milk by their parents. (Full article...)

    In Prospect Park, New York, USA

    The mourning dove (Zenaida macroura) is a member of the dove family, Columbidae. The bird is also known as the American mourning dove, the rain dove, the chueybird, colloquially as the turtle dove, and it was once known as the Carolina pigeon and Carolina turtledove. It is one of the most abundant and widespread North American birds and a popular gamebird, with more than 20 million birds (up to 70 million in some years) shot annually in the U.S., both for sport and meat. Its ability to sustain its population under such pressure is due to its prolific breeding; in warm areas, one pair may raise up to six broods of two young each in a single year. The wings make an unusual whistling sound upon take-off and landing, a form of sonation. The bird is a strong flier, capable of speeds up to 88 km/h (55 mph).

    Mourning doves are light gray and brown and generally muted in color. Males and females are similar in appearance. The species is generally monogamous, with two squabs (young) per brood. Both parents incubate and care for the young. Mourning doves eat almost exclusively seeds, but the young are fed crop milk by their parents. (Full article...)
  • Image 8 male The flame robin (Petroica phoenicea) is a small passerine bird native to Australia. It is a moderately common resident of the coolest parts of south-eastern Australia, including Tasmania. Like the other two red-breasted Petroica robins—the scarlet robin and the red-capped robin—it is often simply called the robin redbreast. Like many brightly coloured robins of the Petroicidae, it is sexually dimorphic. Measuring 12–14 cm (4.7–5.5 in) long, the flame robin has dark brown eyes and a small thin black bill. The male has a brilliant orange-red chest and throat, and a white patch on the forehead above the bill. Its upper parts are iron-grey with white bars, and its tail black with white tips. Female coloration is a muted grey-brown. Its song has been described as the most musical of its genus. The position of the flame robin and its Australian relatives on the passerine family tree is unclear; the Petroicidae are not closely related to either the European or American robins, but appear to be an early offshoot of the Passerida group of songbirds. The flame robin is predominantly insectivorous, pouncing on prey from a perch in a tree, or foraging on the ground. A territorial bird, the flame robin employs song and plumage displays to mark out and defend its territory. It is classified by BirdLife International as least concern. (Full article...)

    male

    The flame robin (Petroica phoenicea) is a small passerine bird native to Australia. It is a moderately common resident of the coolest parts of south-eastern Australia, including Tasmania. Like the other two red-breasted Petroica robins—the scarlet robin and the red-capped robin—it is often simply called the robin redbreast. Like many brightly coloured robins of the Petroicidae, it is sexually dimorphic. Measuring 12–14 cm (4.7–5.5 in) long, the flame robin has dark brown eyes and a small thin black bill. The male has a brilliant orange-red chest and throat, and a white patch on the forehead above the bill. Its upper parts are iron-grey with white bars, and its tail black with white tips. Female coloration is a muted grey-brown. Its song has been described as the most musical of its genus.

    The position of the flame robin and its Australian relatives on the passerine family tree is unclear; the Petroicidae are not closely related to either the European or American robins, but appear to be an early offshoot of the Passerida group of songbirds. The flame robin is predominantly insectivorous, pouncing on prey from a perch in a tree, or foraging on the ground. A territorial bird, the flame robin employs song and plumage displays to mark out and defend its territory. It is classified by BirdLife International as least concern. (Full article...)
  • Image 9 In Tasmania The white-bellied sea eagle (Icthyophaga leucogaster), also known as the white-breasted sea eagle, is a large diurnal bird of prey in the family Accipitridae. Originally described by Johann Friedrich Gmelin in 1788, it is closely related to Sanford's sea eagle of the Solomon Islands, and the two are considered a superspecies. A distinctive bird, the adult white-bellied sea eagle has a white head, breast, under-wing coverts and tail. The upper parts are grey and the black under-wing flight feathers contrast with the white coverts. The tail is short and wedge-shaped as in all Haliaeetinae species. Like many raptors, the female is larger than the male, and can measure up to 90 cm (35 in) long with a wingspan of up to 2.2 m (7.2 ft), and weigh 4.5 kg (9.9 lb). Immature birds have brown plumage, which is gradually replaced by white until the age of five or six years. The call is a loud goose-like honking. Resident from India and Sri Lanka through Southeast Asia to Australia on coasts and major waterways, the white-bellied sea eagle breeds and hunts near water, and fish form around half of its diet. Opportunistic, it consumes carrion and a wide variety of animals. Although rated as Least Concern globally, it has declined in parts of southeast Asia such as Thailand, and southeastern Australia. It is ranked as Threatened in Victoria and Vulnerable in South Australia and Tasmania. Human disturbance to its habitat is the main threat, both from direct human activity near nests which impacts on breeding success, and from removal of suitable trees for nesting. The white-bellied sea eagle is revered by indigenous people in many parts of Australia, and is the subject of various folk tales throughout its range. (Full article...)

    In Tasmania

    The white-bellied sea eagle (Icthyophaga leucogaster), also known as the white-breasted sea eagle, is a large diurnal bird of prey in the family Accipitridae. Originally described by Johann Friedrich Gmelin in 1788, it is closely related to Sanford's sea eagle of the Solomon Islands, and the two are considered a superspecies. A distinctive bird, the adult white-bellied sea eagle has a white head, breast, under-wing coverts and tail. The upper parts are grey and the black under-wing flight feathers contrast with the white coverts. The tail is short and wedge-shaped as in all Haliaeetinae species. Like many raptors, the female is larger than the male, and can measure up to 90 cm (35 in) long with a wingspan of up to 2.2 m (7.2 ft), and weigh 4.5 kg (9.9 lb). Immature birds have brown plumage, which is gradually replaced by white until the age of five or six years. The call is a loud goose-like honking.

    Resident from India and Sri Lanka through Southeast Asia to Australia on coasts and major waterways, the white-bellied sea eagle breeds and hunts near water, and fish form around half of its diet. Opportunistic, it consumes carrion and a wide variety of animals. Although rated as Least Concern globally, it has declined in parts of southeast Asia such as Thailand, and southeastern Australia. It is ranked as Threatened in Victoria and Vulnerable in South Australia and Tasmania. Human disturbance to its habitat is the main threat, both from direct human activity near nests which impacts on breeding success, and from removal of suitable trees for nesting. The white-bellied sea eagle is revered by indigenous people in many parts of Australia, and is the subject of various folk tales throughout its range. (Full article...)
  • Image 10 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 11 Coloeus monedula Western jackdaw calls (Estonia) The western jackdaw (Coloeus monedula), also known as the Eurasian jackdaw, the European jackdaw, or simply the jackdaw, is a passerine bird in the crow family. Found across Europe, western Asia and North Africa; it is mostly resident, although northern and eastern populations migrate south in the winter. Four subspecies are recognised, which differ mainly in the colouration of the plumage on the head and nape. Linnaeus first described it formally, giving it the name Corvus monedula. The common name derives from the word jack, denoting "small", and daw, a less common synonym for "jackdaw", and the native English name for the bird. Measuring 34–39 centimetres (13–15 in) in length, the western jackdaw is a black-plumaged bird with a grey nape and distinctive pale-grey irises. It is gregarious and vocal, living in small groups with a complex social structure in farmland, open woodland, on coastal cliffs, and in urban settings. Like its relatives, jackdaws are intelligent birds, and have been observed using tools. An omnivorous and opportunistic feeder, it eats a wide variety of plant material and invertebrates, as well as food waste from urban areas. Western jackdaws are monogamous and build simple nests of sticks in cavities in trees, cliffs, or buildings. About five pale blue or blue-green eggs with brown speckles are laid and incubated by the female. The young fledge in four to five weeks. (Full article...)

    Coloeus monedula
    Western jackdaw calls (Estonia)

    The western jackdaw (Coloeus monedula), also known as the Eurasian jackdaw, the European jackdaw, or simply the jackdaw, is a passerine bird in the crow family. Found across Europe, western Asia and North Africa; it is mostly resident, although northern and eastern populations migrate south in the winter. Four subspecies are recognised, which differ mainly in the colouration of the plumage on the head and nape. Linnaeus first described it formally, giving it the name Corvus monedula. The common name derives from the word jack, denoting "small", and daw, a less common synonym for "jackdaw", and the native English name for the bird.

    Measuring 34–39 centimetres (13–15 in) in length, the western jackdaw is a black-plumaged bird with a grey nape and distinctive pale-grey irises. It is gregarious and vocal, living in small groups with a complex social structure in farmland, open woodland, on coastal cliffs, and in urban settings. Like its relatives, jackdaws are intelligent birds, and have been observed using tools. An omnivorous and opportunistic feeder, it eats a wide variety of plant material and invertebrates, as well as food waste from urban areas. Western jackdaws are monogamous and build simple nests of sticks in cavities in trees, cliffs, or buildings. About five pale blue or blue-green eggs with brown speckles are laid and incubated by the female. The young fledge in four to five weeks. (Full article...)
  • Image 12 The black-throated loon (Gavia arctica), also known as the Arctic loon and the black-throated diver, is a migratory aquatic bird found in the northern hemisphere, primarily breeding in freshwater lakes in northern Europe and Asia. It winters along sheltered, ice-free coasts of the north-east Atlantic Ocean and the eastern and western Pacific Ocean. This loon was first described by Carl Linnaeus in 1758 and has two subspecies. It was previously considered to be the same species as the Pacific loon, of which it is traditionally considered to be a sister species, although this is debated. In a study that used mitochondrial and nuclear intron DNA, the black-throated loon was found to be sister to a clade consisting of the Pacific loon and two sister species, the common loon and the yellow-billed loon. The black-throated loon measures about 70 cm (28 in) in length and can weigh anywhere from 1.3 to 3.4 kilograms (2.9 to 7.5 lb). In breeding plumage, the adult of the nominate subspecies has mostly black upperparts, with the exception of some of the mantle and scapulars, which have white squares. The head and hindneck are grey, and the sides white and striped black. Most of the throat is also black, giving this bird the name "black-throated loon". The colour of the throat patch can be used to distinguish the two subspecies; the throat patch of the other subspecies, G. a. viridigularis, is green. The underparts are mostly white, including the bottom of the throat. The flanks are also white, a feature which can be used to separate this bird from the Pacific loon. When the bird is not breeding, the black patch on the throat is absent, replaced with white; most of the black lines on the throat are also missing, except those on the bottom sides, and the upperparts are unpatterned with the exception of a few white spots on the upperwing. The juvenile is similar to the non-breeding adult, except more brown overall. The timing of the breeding season is variable; in the southern part of its range, this loon starts breeding in April, whereas in the northern portion, it waits until after the spring thaw. It builds an oval nest about 23 centimetres (9.1 in) across, either near the breeding lake or on vegetation emerging from it. The black-throated loon usually lays a clutch of two, rarely one or three, brown-green eggs with dark splotches. After an incubation period of 27 to 29 days, the chick hatches, and is fed a diet of small fish and invertebrates. The adult mostly eats fish. To catch this food, it forages by itself or in pairs, very rarely foraging in groups. It dives from the water, going no deeper than 5 metres (16 ft). Most dives are successful. Whether or not at least one chick will hatch from a nest is variable, ranging from 30% to 90%. Most failures come from predators and flooding. Overall, the population of this loon is declining, although the International Union for Conservation of Nature (IUCN) still rates it as least concern, because the population decline is not rapid enough. The black-throated loon is protected under both the Migratory Bird Treaty Act of 1918 and the Agreement on the Conservation of African-Eurasian Migratory Waterbirds. (Full article...)

    The black-throated loon (Gavia arctica), also known as the Arctic loon and the black-throated diver, is a migratory aquatic bird found in the northern hemisphere, primarily breeding in freshwater lakes in northern Europe and Asia. It winters along sheltered, ice-free coasts of the north-east Atlantic Ocean and the eastern and western Pacific Ocean. This loon was first described by Carl Linnaeus in 1758 and has two subspecies. It was previously considered to be the same species as the Pacific loon, of which it is traditionally considered to be a sister species, although this is debated. In a study that used mitochondrial and nuclear intron DNA, the black-throated loon was found to be sister to a clade consisting of the Pacific loon and two sister species, the common loon and the yellow-billed loon.

    The black-throated loon measures about 70 cm (28 in) in length and can weigh anywhere from 1.3 to 3.4 kilograms (2.9 to 7.5 lb). In breeding plumage, the adult of the nominate subspecies has mostly black upperparts, with the exception of some of the mantle and scapulars, which have white squares. The head and hindneck are grey, and the sides white and striped black. Most of the throat is also black, giving this bird the name "black-throated loon". The colour of the throat patch can be used to distinguish the two subspecies; the throat patch of the other subspecies, G. a. viridigularis, is green. The underparts are mostly white, including the bottom of the throat. The flanks are also white, a feature which can be used to separate this bird from the Pacific loon. When the bird is not breeding, the black patch on the throat is absent, replaced with white; most of the black lines on the throat are also missing, except those on the bottom sides, and the upperparts are unpatterned with the exception of a few white spots on the upperwing. The juvenile is similar to the non-breeding adult, except more brown overall.

    The timing of the breeding season is variable; in the southern part of its range, this loon starts breeding in April, whereas in the northern portion, it waits until after the spring thaw. It builds an oval nest about 23 centimetres (9.1 in) across, either near the breeding lake or on vegetation emerging from it. The black-throated loon usually lays a clutch of two, rarely one or three, brown-green eggs with dark splotches. After an incubation period of 27 to 29 days, the chick hatches, and is fed a diet of small fish and invertebrates. The adult mostly eats fish. To catch this food, it forages by itself or in pairs, very rarely foraging in groups. It dives from the water, going no deeper than 5 metres (16 ft). Most dives are successful. Whether or not at least one chick will hatch from a nest is variable, ranging from 30% to 90%. Most failures come from predators and flooding. Overall, the population of this loon is declining, although the International Union for Conservation of Nature (IUCN) still rates it as least concern, because the population decline is not rapid enough. The black-throated loon is protected under both the Migratory Bird Treaty Act of 1918 and the Agreement on the Conservation of African-Eurasian Migratory Waterbirds. (Full article...)
  • Image 13 At William Bay, Western Australia The rock parrot (Neophema petrophila) is a species of grass parrot native to Australia. Described by John Gould in 1841, it is a small parrot 22–24 cm (8+3⁄4–9+1⁄2 in) long and weighing 50–60 g (1+3⁄4–2 oz) with predominantly olive-brown upperparts and more yellowish underparts. Its head is olive with light blue forecheeks and lores, and a dark blue frontal band line across the crown with lighter blue above and below. The sexes are similar in appearance, although the female tends to have a duller frontal band and less blue on the face. The female's call also tends to be far louder and more shrill than the male's. Two subspecies are currently recognised. Rocky islands and coastal dune areas are the preferred habitats for this species, which is found from Lake Alexandrina in southeastern South Australia westwards across coastal South and Western Australia to Shark Bay. Unlike other grass parrots, it nests in burrows or rocky crevices mostly on offshore islands such as Rottnest Island. Seeds of grasses and succulent plants form the bulk of its diet. The species has suffered in the face of feral mammals; although its population is declining, it is considered to be a least-concern species by the International Union for Conservation of Nature (IUCN). (Full article...)

    At William Bay, Western Australia

    The rock parrot (Neophema petrophila) is a species of grass parrot native to Australia. Described by John Gould in 1841, it is a small parrot 22–24 cm (8+3⁄4–9+1⁄2 in) long and weighing 50–60 g (1+3⁄4–2 oz) with predominantly olive-brown upperparts and more yellowish underparts. Its head is olive with light blue forecheeks and lores, and a dark blue frontal band line across the crown with lighter blue above and below. The sexes are similar in appearance, although the female tends to have a duller frontal band and less blue on the face. The female's call also tends to be far louder and more shrill than the male's. Two subspecies are currently recognised.

    Rocky islands and coastal dune areas are the preferred habitats for this species, which is found from Lake Alexandrina in southeastern South Australia westwards across coastal South and Western Australia to Shark Bay. Unlike other grass parrots, it nests in burrows or rocky crevices mostly on offshore islands such as Rottnest Island. Seeds of grasses and succulent plants form the bulk of its diet. The species has suffered in the face of feral mammals; although its population is declining, it is considered to be a least-concern species by the International Union for Conservation of Nature (IUCN). (Full article...)
  • Image 14 Adult in Mangily, Madagascar The long-tailed ground roller (Uratelornis chimaera) is a species of bird in the ground roller family Brachypteraciidae, placed in the monotypic genus Uratelornis. Endemic to arid spiny forests near the coast in southwestern Madagascar, this ground roller occurs at extremely low population densities throughout its habitat. This species requires shade and a deep layer of leaves on the ground, and it is absent from parts of the spiny forest lacking these features. It has no recognized subspecies, and its closest relative is the scaly ground roller. The long-tailed ground roller is the only ground roller to definitively display sexual dimorphism (differences in plumage or size between sexes). It is a medium-sized bird with a plump silhouette and a long tail. The upperparts are dark brown with black streaks while the underparts are light gray. The white throat is framed by black malar stripes and a black breastband, and a white stripe is present at the base of the bill. Sky-blue feathers are visible at the edge of the wings and the tail. Calls are rarely made outside the breeding season, though multiple courtship calls are made. These ground rollers feed primarily on invertebrates, including ants, beetles, butterflies, and worms, which they find by searching through deep leaf litter or by remaining still and watching attentively. The ground roller primarily runs through its habitat on its strong legs, as its wings are relatively weak. It is a monogamous species, and it defends a territory during the breeding season of October to February. It digs a tunnel in the sand, at the end of which is a wider chamber where it makes its nest out of leaves and earthy pellets. Two to four eggs are laid. After the chicks fledge, the birds continue living in family groups until at least February before dispersing more widely across the scrubland. This bird is classified as vulnerable by the IUCN and is threatened by habitat destruction. Since the arid, spiny forests in which it lives are not protected by the Malagasy government, it is losing habitat to slash-and-burn agriculture, charcoal collection, and logging. It is also hunted by the native peoples of Madagascar. (Full article...)

    Adult in Mangily, Madagascar

    The long-tailed ground roller (Uratelornis chimaera) is a species of bird in the ground roller family Brachypteraciidae, placed in the monotypic genus Uratelornis. Endemic to arid spiny forests near the coast in southwestern Madagascar, this ground roller occurs at extremely low population densities throughout its habitat. This species requires shade and a deep layer of leaves on the ground, and it is absent from parts of the spiny forest lacking these features. It has no recognized subspecies, and its closest relative is the scaly ground roller. The long-tailed ground roller is the only ground roller to definitively display sexual dimorphism (differences in plumage or size between sexes). It is a medium-sized bird with a plump silhouette and a long tail. The upperparts are dark brown with black streaks while the underparts are light gray. The white throat is framed by black malar stripes and a black breastband, and a white stripe is present at the base of the bill. Sky-blue feathers are visible at the edge of the wings and the tail. Calls are rarely made outside the breeding season, though multiple courtship calls are made.

    These ground rollers feed primarily on invertebrates, including ants, beetles, butterflies, and worms, which they find by searching through deep leaf litter or by remaining still and watching attentively. The ground roller primarily runs through its habitat on its strong legs, as its wings are relatively weak. It is a monogamous species, and it defends a territory during the breeding season of October to February. It digs a tunnel in the sand, at the end of which is a wider chamber where it makes its nest out of leaves and earthy pellets. Two to four eggs are laid. After the chicks fledge, the birds continue living in family groups until at least February before dispersing more widely across the scrubland.

    This bird is classified as vulnerable by the IUCN and is threatened by habitat destruction. Since the arid, spiny forests in which it lives are not protected by the Malagasy government, it is losing habitat to slash-and-burn agriculture, charcoal collection, and logging. It is also hunted by the native peoples of Madagascar. (Full article...)
  • Image 15 When preening, a bird (such as this red lory) draws individual feathers through its beak, realigning and re-interlocking the barbules. Preening is a maintenance behaviour found in birds that involves the use of the beak to position feathers, interlock feather barbules that have become separated, clean plumage, and keep ectoparasites in check. Feathers contribute significantly to a bird's insulation, waterproofing and aerodynamic flight, and so are vital to its survival. Because of this, birds spend considerable time each day maintaining their feathers, primarily through preening. Several actions make up preening behaviour. Birds fluff up and shake their feathers, which helps to "rezip" feather barbules that have become unhooked. Using their beaks, they gather preen oil from a gland at the base of their tail and distribute this oil through their feathers. They draw each contour feather through their bill, nibbling it from base to tip. Over time, some elements of preening have evolved to have secondary functions. Ritualised preening has become a part of some courtship displays, for example. It is also a displacement activity that can occur when birds are subjected to two conflicting drives. Though primarily an individual function, preening can be a social activity involving two or more birds – a behaviour known as allopreening. In general, allopreening occurs either between two members of a mated pair or between flock members in a social species. Such behaviour may assist in effective grooming, in the recognition of individuals (mates or potential sexual partners), or in reducing or redirecting potential aggressive tendencies in social species. Most allopreening is confined to the head and neck, smaller efforts being directed towards other parts of the body. Ingestion of pollutants or disease-causing organisms during preening can lead to problems ranging from liver and kidney damage to pneumonia and disease transmission. Injury and infection can cause overpreening in caged birds, as can confining a bird with a dominant or aggressive cage mate. (Full article...)
    The head and back of a short-billed red parrot, which is chewing on the tip of a black and red feather
    When preening, a bird (such as this red lory) draws individual feathers through its beak, realigning and re-interlocking the barbules.


    Preening is a maintenance behaviour found in birds that involves the use of the beak to position feathers, interlock feather barbules that have become separated, clean plumage, and keep ectoparasites in check. Feathers contribute significantly to a bird's insulation, waterproofing and aerodynamic flight, and so are vital to its survival. Because of this, birds spend considerable time each day maintaining their feathers, primarily through preening. Several actions make up preening behaviour. Birds fluff up and shake their feathers, which helps to "rezip" feather barbules that have become unhooked. Using their beaks, they gather preen oil from a gland at the base of their tail and distribute this oil through their feathers. They draw each contour feather through their bill, nibbling it from base to tip.

    Over time, some elements of preening have evolved to have secondary functions. Ritualised preening has become a part of some courtship displays, for example. It is also a displacement activity that can occur when birds are subjected to two conflicting drives. Though primarily an individual function, preening can be a social activity involving two or more birds – a behaviour known as allopreening. In general, allopreening occurs either between two members of a mated pair or between flock members in a social species. Such behaviour may assist in effective grooming, in the recognition of individuals (mates or potential sexual partners), or in reducing or redirecting potential aggressive tendencies in social species. Most allopreening is confined to the head and neck, smaller efforts being directed towards other parts of the body.

    Ingestion of pollutants or disease-causing organisms during preening can lead to problems ranging from liver and kidney damage to pneumonia and disease transmission. Injury and infection can cause overpreening in caged birds, as can confining a bird with a dominant or aggressive cage mate. (Full article...)
  • Image 16 Messiaen in 1986 Olivier Eugène Prosper Charles Messiaen (UK: /ˈmɛsiæ̃/, US: /mɛˈsjæ̃, meɪˈsjæ̃, mɛˈsjɒ̃/; French: [ɔlivje øʒɛn pʁɔspɛʁ ʃaʁl mɛsjɑ̃]; 10 December 1908 – 27 April 1992) was a French composer, organist, and ornithologist. One of the major composers of the 20th century, he was also an outstanding teacher of composition and musical analysis. Messiaen entered the Paris Conservatoire at age 11 and studied with Paul Dukas, Maurice Emmanuel, Charles-Marie Widor and Marcel Dupré, among others. He was appointed organist at the Église de la Sainte-Trinité, Paris, in 1931, a post he held for 61 years, until his death. He taught at the Schola Cantorum de Paris during the 1930s. After the fall of France in 1940, Messiaen was interned for nine months in the German prisoner of war camp Stalag VIII-A, where he composed his Quatuor pour la fin du temps (Quartet for the End of Time) for the four instruments available in the prison—piano, violin, cello and clarinet. The piece was first performed by Messiaen and fellow prisoners for an audience of inmates and prison guards. Soon after his release in 1941, Messiaen was appointed professor of harmony at the Paris Conservatoire. In 1966, he was appointed professor of composition there, and he held both positions until retiring in 1978. His many distinguished pupils included Iannis Xenakis, George Benjamin, Alexander Goehr, Pierre Boulez, Jacques Hétu, Tristan Murail, Karlheinz Stockhausen, György Kurtág, and Yvonne Loriod, who became his second wife. Messiaen perceived colours when he heard certain musical chords (a phenomenon known as chromesthesia); according to him, combinations of these colours were important in his compositional process. He travelled widely and wrote works inspired by diverse influences, including Japanese music, the landscape of Bryce Canyon in Utah, and the life of St. Francis of Assisi. His style absorbed many global musical influences, such as Indonesian gamelan (tuned percussion often features prominently in his orchestral works). He found birdsong fascinating, notating bird songs worldwide and incorporating birdsong transcriptions into his music. (Full article...)

    Messiaen in 1986

    Olivier Eugène Prosper Charles Messiaen (UK: /ˈmɛsiæ̃/, US: /mɛˈsjæ̃, meɪˈsjæ̃, mɛˈsjɒ̃/; French: [ɔlivje øʒɛn pʁɔspɛʁ ʃaʁl mɛsjɑ̃]; 10 December 1908 – 27 April 1992) was a French composer, organist, and ornithologist. One of the major composers of the 20th century, he was also an outstanding teacher of composition and musical analysis.


    Messiaen entered the Paris Conservatoire at age 11 and studied with Paul Dukas, Maurice Emmanuel, Charles-Marie Widor and Marcel Dupré, among others. He was appointed organist at the Église de la Sainte-Trinité, Paris, in 1931, a post he held for 61 years, until his death. He taught at the Schola Cantorum de Paris during the 1930s. After the fall of France in 1940, Messiaen was interned for nine months in the German prisoner of war camp Stalag VIII-A, where he composed his Quatuor pour la fin du temps (Quartet for the End of Time) for the four instruments available in the prison—piano, violin, cello and clarinet. The piece was first performed by Messiaen and fellow prisoners for an audience of inmates and prison guards. Soon after his release in 1941, Messiaen was appointed professor of harmony at the Paris Conservatoire. In 1966, he was appointed professor of composition there, and he held both positions until retiring in 1978. His many distinguished pupils included Iannis Xenakis, George Benjamin, Alexander Goehr, Pierre Boulez, Jacques Hétu, Tristan Murail, Karlheinz Stockhausen, György Kurtág, and Yvonne Loriod, who became his second wife.


    Messiaen perceived colours when he heard certain musical chords (a phenomenon known as chromesthesia); according to him, combinations of these colours were important in his compositional process. He travelled widely and wrote works inspired by diverse influences, including Japanese music, the landscape of Bryce Canyon in Utah, and the life of St. Francis of Assisi. His style absorbed many global musical influences, such as Indonesian gamelan (tuned percussion often features prominently in his orchestral works). He found birdsong fascinating, notating bird songs worldwide and incorporating birdsong transcriptions into his music. (Full article...)
  • Image 17 The Perijá tapaculo (Scytalopus perijanus) is a species of passerine bird in the family Rhinocryptidae (tapaculos). Endemic to the Serranía del Perijá mountain range on the Colombia–Venezuela border, the Perijá tapaculo is found at altitudes of 1,600–3,225 metres (5,200–10,600 feet). Its body is 10 to 12 centimetres (3.9 to 4.7 inches) long and its tail is about 4 cm (1.6 in) long. Specimens have long been stored in museums, but the species was described only in 2015 based on sixteen specimens found between July 2008 and February 2009. It is considered vulnerable to extinction. Adults have neutral grey heads, brown necks, brown-sepia striped backs, and grey-white bellies, breasts, and throats. Males have some buff markings on their breasts, and less sharp brown spots on their napes than females. The Perijá tapaculo is a secretive bird and therefore difficult to observe; as a result its ecology is poorly known. It feeds on insects and reproduces between April and July. Its range is partially within Chamicero de Perijá Bird Reserve in Colombia and the Sierra de Perijá National Park in Venezuela. (Full article...)

    The Perijá tapaculo (Scytalopus perijanus) is a species of passerine bird in the family Rhinocryptidae (tapaculos). Endemic to the Serranía del Perijá mountain range on the Colombia–Venezuela border, the Perijá tapaculo is found at altitudes of 1,600–3,225 metres (5,200–10,600 feet). Its body is 10 to 12 centimetres (3.9 to 4.7 inches) long and its tail is about 4 cm (1.6 in) long. Specimens have long been stored in museums, but the species was described only in 2015 based on sixteen specimens found between July 2008 and February 2009. It is considered vulnerable to extinction.

    Adults have neutral grey heads, brown necks, brown-sepia striped backs, and grey-white bellies, breasts, and throats. Males have some buff markings on their breasts, and less sharp brown spots on their napes than females. The Perijá tapaculo is a secretive bird and therefore difficult to observe; as a result its ecology is poorly known. It feeds on insects and reproduces between April and July. Its range is partially within Chamicero de Perijá Bird Reserve in Colombia and the Sierra de Perijá National Park in Venezuela. (Full article...)
  • Image 18 The pied butcherbird (Cracticus nigrogularis) is a songbird native to Australia. Described by John Gould in 1837, it is a black and white bird 28 to 32 cm (11 to 12.5 in) long with a long hooked bill. Its head and throat are black, making a distinctive hood; the mantle and much of the tail and wings are also black. The neck, underparts and outer wing feathers are white. The juvenile and immature birds are predominantly brown and white. As they mature their brown feathers are replaced by black feathers. There are two recognised subspecies of pied butcherbird. Within its range, the pied butcherbird is generally sedentary. Common in woodlands and in urban environments, it is carnivorous, eating insects and small vertebrates including birds. A tame and inquisitive bird, the pied butcherbird has been known to accept food from humans. It nests in trees, constructing a cup-shaped structure out of sticks and laying two to five eggs. The pied butcherbird engages in cooperative breeding, with a mated pair sometimes assisted by several helper birds. The troop is territorial, defending the nesting site from intruders. The International Union for Conservation of Nature (IUCN) has assessed the pied butcherbird as being of least concern on account of its large range and apparently stable population. (Full article...)

    The pied butcherbird (Cracticus nigrogularis) is a songbird native to Australia. Described by John Gould in 1837, it is a black and white bird 28 to 32 cm (11 to 12.5 in) long with a long hooked bill. Its head and throat are black, making a distinctive hood; the mantle and much of the tail and wings are also black. The neck, underparts and outer wing feathers are white. The juvenile and immature birds are predominantly brown and white. As they mature their brown feathers are replaced by black feathers. There are two recognised subspecies of pied butcherbird.

    Within its range, the pied butcherbird is generally sedentary. Common in woodlands and in urban environments, it is carnivorous, eating insects and small vertebrates including birds. A tame and inquisitive bird, the pied butcherbird has been known to accept food from humans. It nests in trees, constructing a cup-shaped structure out of sticks and laying two to five eggs. The pied butcherbird engages in cooperative breeding, with a mated pair sometimes assisted by several helper birds. The troop is territorial, defending the nesting site from intruders. The International Union for Conservation of Nature (IUCN) has assessed the pied butcherbird as being of least concern on account of its large range and apparently stable population. (Full article...)
  • Image 19 Subspecies cyanotis, Queensland The blue-faced honeyeater (Entomyzon cyanotis), also colloquially known as the Bananabird, is a passerine bird of the honeyeater family, Meliphagidae. It is the only member of its genus, and it is most closely related to honeyeaters of the genus Melithreptus. Three subspecies are recognised. At around 29.5 cm (11.6 in) in length, the blue-faced species is large for a honeyeater. Its plumage is distinctive, with olive upperparts, white underparts, and a black head and throat with white nape and cheeks. Males and females are similar in external appearance. Adults have a blue area of bare skin on each side of the face readily distinguishing them from juveniles, which have yellow or green patches of bare skin.Found in open woodland, parks and gardens, the blue-faced honeyeater is common in northern and eastern Australia, and southern New Guinea. It appears to be sedentary in parts of its range, and locally nomadic in other parts; however, the species has been little studied. Its diet is mostly composed of invertebrates, supplemented with nectar and fruit. They often take over and renovate old babbler nests, in which the female lays and incubates two or rarely three eggs. (Full article...)

    Subspecies cyanotis, Queensland

    The blue-faced honeyeater (Entomyzon cyanotis), also colloquially known as the Bananabird, is a passerine bird of the honeyeater family, Meliphagidae. It is the only member of its genus, and it is most closely related to honeyeaters of the genus Melithreptus. Three subspecies are recognised. At around 29.5 cm (11.6 in) in length, the blue-faced species is large for a honeyeater. Its plumage is distinctive, with olive upperparts, white underparts, and a black head and throat with white nape and cheeks. Males and females are similar in external appearance. Adults have a blue area of bare skin on each side of the face readily distinguishing them from juveniles, which have yellow or green patches of bare skin.Found in open woodland, parks and gardens, the blue-faced honeyeater is common in northern and eastern Australia, and southern New Guinea. It appears to be sedentary in parts of its range, and locally nomadic in other parts; however, the species has been little studied. Its diet is mostly composed of invertebrates, supplemented with nectar and fruit. They often take over and renovate old babbler nests, in which the female lays and incubates two or rarely three eggs. (Full article...)
  • Image 20 Male perched on a mangrove branch The red-headed myzomela or red-headed honeyeater (Myzomela erythrocephala) is a passerine bird of the honeyeater family Meliphagidae found in Australia, Indonesia, and Papua New Guinea. It was described by John Gould in 1840. Two subspecies are recognised, with the nominate race M. e. erythrocephala distributed around the tropical coastline of Australia, and M. e. infuscata in New Guinea. Though widely distributed, the species is not abundant within this range. While the IUCN lists the Australian population of M. e. infuscata as being near threatened, as a whole the widespread range means that its conservation is of least concern. At 12 cm (4.7 in), it is a small honeyeater with a short tail and relatively long down-curved bill. It is sexually dimorphic; the male has a glossy red head and brown upperparts and paler grey-brown underparts while the female has predominantly grey-brown plumage. Its natural habitat is subtropical or tropical mangrove forests. It is very active when feeding in the tree canopy, darting from flower to flower and gleaning insects off foliage. It calls constantly as it feeds. While little has been documented on the red-headed myzomela's breeding behaviour, it is recorded as building a small cup-shaped nest in the mangroves and laying two or three oval, white eggs with small red blotches. (Full article...)

    Male perched on a mangrove branch

    The red-headed myzomela or red-headed honeyeater (Myzomela erythrocephala) is a passerine bird of the honeyeater family Meliphagidae found in Australia, Indonesia, and Papua New Guinea. It was described by John Gould in 1840. Two subspecies are recognised, with the nominate race M. e. erythrocephala distributed around the tropical coastline of Australia, and M. e. infuscata in New Guinea. Though widely distributed, the species is not abundant within this range. While the IUCN lists the Australian population of M. e. infuscata as being near threatened, as a whole the widespread range means that its conservation is of least concern.

    At 12 cm (4.7 in), it is a small honeyeater with a short tail and relatively long down-curved bill. It is sexually dimorphic; the male has a glossy red head and brown upperparts and paler grey-brown underparts while the female has predominantly grey-brown plumage. Its natural habitat is subtropical or tropical mangrove forests. It is very active when feeding in the tree canopy, darting from flower to flower and gleaning insects off foliage. It calls constantly as it feeds. While little has been documented on the red-headed myzomela's breeding behaviour, it is recorded as building a small cup-shaped nest in the mangroves and laying two or three oval, white eggs with small red blotches. (Full article...)
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Bird kill is a localized event resulting in the death of large numbers of birds at the same time. (Full article...)

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Adult male Bullock's oriole

Icterids (/ˈɪktərɪd/) or New World blackbirds make up a family, the Icteridae (/ɪkˈtɛrɪdi/), of small to medium-sized, often colorful, New World passerine birds. The family contains 108 species and is divided into 30 genera. Most species have black as a predominant plumage color, often enlivened by yellow, orange, or red. The species in the family vary widely in size, shape, behavior, and coloration. The name, meaning "jaundiced ones" (from the prominent yellow feathers of many species) comes from the Ancient Greek ikteros via the Latin ictericus. This group includes the New World blackbirds, New World orioles, the bobolink, meadowlarks, grackles, cowbirds, oropendolas, and caciques.

Despite the similar names, the first groups are only distantly related to the Old World common blackbird (a thrush) or the Old World orioles.

The Icteridae are not to be confused with the Icteriidae, a family created in 2017 and consisting of one species — the yellow-breasted chat (Icteria virens). (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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For more sources, including printed sources, see WikiProject Birds.

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Patagia on a flying squirrel

The patagium (pl.: patagia) is a membranous body part that assists an animal in obtaining lift when gliding or flying. The structure is found in extant and extinct groups of flying and gliding animals including bats, theropod dinosaurs (including birds and some dromaeosaurs), pterosaurs, gliding mammals, some flying lizards, and flying frogs. The patagium that stretches between an animal's hind limbs is called the uropatagium (especially in bats) or the interfemoral membrane. (Full article...)

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A male splendid fairy-wren (subsp. splendens)
The splendid fairy-wren (Malurus splendens), also known simply as the splendid wren or more colloquially in Western Australia as the blue wren, is a passerine bird of the family Maluridae. It is found across much of the Australian continent from central-western New South Wales and southwestern Queensland over to coastal Western Australia. The male in breeding plumage is a small, long-tailed bird of predominantly bright blue and black colouration. Non-breeding males, females and juveniles are predominantly grey-brown in colour. It comprises several similar all-blue and black subspecies that were originally considered separate species. Like other fairy-wrens, the splendid fairy-wren is notable for several peculiar behavioural characteristics; birds are socially monogamous and sexually promiscuous. Male wrens pluck pink or purple petals and display them to females as part of a courtship display. The habitat of the splendid fairy-wren ranges from forest to dry scrub, generally with ample vegetation for shelter. It has not adapted well to human occupation of the landscape and has disappeared from some urbanized areas. The splendid fairy-wren mainly eats insects and supplements its diet with seeds.


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Did you know

  • ...that sexual size dimorphism in the brown songlark is among the most pronounced in any bird, with males as much as 2.3 times heavier than females?
  • ...that rufous whistler birds, unlike all other whistler birds, never forage on the ground but high up in trees or other high places?
  • ...that the bill of the magpie duck (pictured) becomes green as the bird gets older, and its black crown may go completely white?
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Taxonomy of Aves

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Sources

  1. ^ Mead, D., ed. (1848). The American Literary Emporium. New York, NY, US: C. H. Camp. p. 209.
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