Everything about Birds totally explained
Late
Jurassic – Recent
| image = Phalacrocorax-auritus-007.jpg
| image_width = 240px
| image_caption =
Double-crested Cormorant,
Phalacrocorax auritus
| regnum =
Animalia
| phylum =
Chordata
| subphylum =
Vertebrata
| unranked_classis =
Archosauria
| classis =
Aves
| classis_authority =
Linnaeus, 1758
| subdivision_ranks =
Orders
| subdivision =
About two dozen - see
section below
}}
Birds (
class Aves) are
bipedal, endothermic (
warm-blooded),
vertebrate animals that lay
eggs. There are around 10,000 living species, making them the most numerous
tetrapod vertebrates. They inhabit ecosystems across the globe, from the Arctic to the Antarctic. Birds range in size from the
Bee Hummingbird to the
Ostrich. The fossil record indicates that birds
evolved from
theropod dinosaurs during the
Jurassic period, around 150–200 Ma (million years ago), and the earliest known bird is the Late Jurassic
Archaeopteryx,
c 155–150 Ma. Most
paleontologists regard birds as the only
clade of dinosaurs that survived the
Cretaceous–Tertiary extinction event approximately 65.5 Ma.
Modern birds are
characterised by feathers, a beak with no teeth, the laying of hard-shelled eggs, a high
metabolic rate, a four-chambered heart, and a lightweight but strong
skeleton. All birds have forelimbs modified as wings and most can
fly, with some exceptions including
ratites,
penguins, and a number of diverse
endemic island species. Birds also have unique
digestive and
respiratory systems that are highly adapted for flight. Some birds, especially
corvids and
parrots, are among the most intelligent animal species; a number of bird species have been observed manufacturing and using
tools, and many social species exhibit
cultural transmission of knowledge across generations.
Many species undertake long distance annual
migrations, and many more perform shorter irregular movements. Birds are social; they communicate using visual signals and through calls and
songs, and participate in social behaviours including
cooperative breeding and hunting,
flocking, and
mobbing of predators. The vast majority of bird species are
socially monogamous, usually for one breeding season at a time, sometimes for years, but rarely for life. Other species have breeding systems that are
polygynous ("many females") or, rarely,
polyandrous ("many males"). Eggs are usually laid in a nest and
incubated by the parents. Most birds have an extended period of parental care after hatching.
Many species are of economic importance, mostly as sources of food acquired through hunting or farming. Some species, particularly
songbirds and
parrots, are popular as pets. Other uses include the harvesting of
guano (droppings) for use as a
fertiliser. Birds
figure prominently in all aspects of human culture from religion to poetry to popular music. About 120–130 species have become
extinct as a result of human activity since the 17th century, and hundreds more before then. Currently about 1,200 species of birds are threatened with extinction by human activities, though efforts are underway to
protect them.
Evolution and taxonomy
The first
classification of birds was developed by
Francis Willughby and
John Ray in their 1676 volume
Ornithologiae.
Carolus Linnaeus modified that work in 1758 to devise the taxonomic classification system currently in use.
Birds are categorised as the
biological class Aves in
Linnaean taxonomy.
Phylogenetic taxonomy places Aves in the dinosaur
clade Theropoda.
Aves and a sister group, the clade
Crocodilia, together are the sole living members of the
reptile clade
Archosauria.
Phylogenetically, Aves is commonly defined as all descendants of the most recent common ancestor of modern birds and
Archaeopteryx lithographica.
Archaeopteryx, from the
Kimmeridgian stage of the
Late Jurassic (some 155–150 million years ago), is the earliest known bird under this definition. Others, including
Jacques Gauthier and adherents of the
Phylocode system, have defined Aves to include only the modern bird groups, excluding most groups known only from fossils, and assigning them, instead, to the
Avialae in part to avoid the uncertainties about the placement of
Archaeopteryx in relation to animals traditionally thought of as theropod dinosaurs.
All modern birds lie within the
subclass Neornithes, which has two subdivisions: the
Paleognathae, containing mostly flightless birds like
ostriches, and the wildly diverse
Neognathae, containing all other birds. although Livezey & Zusi assigned them "cohort" rank. to 10,050.
Dinosaurs and the origin of birds
Fossil evidence and intensive biological analyses have demonstrated beyond any reasonable doubt that birds are
theropod
dinosaurs. More specifically, they're members of
Maniraptora, a group of theropods which includes
dromaeosaurs and
oviraptorids, among others. As scientists discover more non-avian theropods that are closely related to birds, the previously clear distinction between non-birds and birds has become blurred. Recent discoveries in the
Liaoning Province of northeast
China, which demonstrate that many small
theropod dinosaurs had feathers, contribute to this ambiguity.
The consensus view in contemporary
paleontology is that the birds,
Aves, are the closest relatives of the
deinonychosaurs, which include
dromaeosaurids and
troodontids. Together, these three form a group called
Paraves. The
basal dromaeosaur Microraptor has features which may have enabled it to glide or fly. The most basal deinonychosaurs are very small. This evidence raises the possibility that the ancestor of all paravians may have been
arboreal, and/or may have been able to glide.
The
Late Jurassic Archaeopteryx is well-known as one of the first
transitional fossils to be found and it provided support for the theory of
evolution in the late 19th century.
Archaeopteryx has clearly reptilian characters: teeth, clawed fingers, and a long, lizard-like tail, but it has finely preserved wings with flight feathers identical to those of modern birds. It isn't considered a direct ancestor of modern birds, but is the oldest and most primitive member of
Aves or
Avialae, and it's probably closely related to the real ancestor. It has even been suggested that
Archaeopteryx was a dinosaur that was no more closely related to birds than were other dinosaur groups, and that
Avimimus was more likely to be the ancestor of all birds than
Archaeopteryx.
Alternative theories and controversies
There have been many controversies in the study of the origin of birds. Early disagreements included whether birds evolved from
dinosaurs or more primitive
archosaurs. Within the dinosaur camp there were disagreements as to whether
ornithischian or
theropod dinosaurs were the more likely ancestors. Although
ornithischian (bird-hipped) dinosaurs share the hip structure of modern birds, birds are thought to have originated from the
saurischian (lizard-hipped) dinosaurs, and therefore evolved their hip structure
independently. In fact, a bird-like hip structure evolved a third time among a peculiar group of theropods known as the
Therizinosauridae.
Scientists
Larry Martin and
Alan Feduccia believe that birds are not dinosaurs, but that birds evolved from early
archosaurs like
Longisquama. The majority of their publications argued that the similarities between birds and
maniraptoran dinosaurs were convergent, and that the two were unrelated. In the late 1990s the evidence that birds were
maniraptorans became almost indisputable, so Martin and Feduccia adopted a modified version of a hypothesis by dinosaur artist
Gregory S. Paul; where maniraptorans are secondarily flightless birds but, in their version, birds evolved directly from
Longisquama. Thus birds are still not dinosaurs, but neither are most of the known species that are currently classified as
theropod dinosaurs.
Maniraptorans are, instead, flightless,
archosaurian, birds. This theory is contested by most
paleontologists. The features cited as evidence of flightlessness are interpreted by mainstream paleontologists as
exaptations, or "pre-adaptations", that
maniraptorans inherited from their common ancestor with birds.
Protoavis texensis, was described in 1991 as a bird older than
Archaeopteryx. Critics have indicated that the fossil is poorly preserved, extensively reconstructed, and may be a
chimera (made up of fossilized bones from several different kinds of animals). The braincase is most likely that of a very early
coelurosaur
Early evolution of birds
Basal bird phylogeny simplified after Chiappe, 2007
Basal divergences of modern birds
based on Sibley-Ahlquist taxonomy
This is a list of the taxonomic orders in the subclass Neornithes, or modern birds. This list uses the traditional classification (the so-called
Clements order), revised by the Sibley-Monroe classification. The
list of birds gives a more detailed summary of the orders, including families.
Subclass Neornithes
Paleognathae:
The radically different Sibley-Monroe classification (
Sibley-Ahlquist taxonomy), based on molecular data, found widespread adoption in a few aspects, as recent molecular, fossil, and anatomical evidence supported the
Galloanserae for example. ]]
Birds live and breed in most terrestrial habitats and on all seven continents, reaching their southern extreme in the
Snow Petrel's breeding colonies up to inland in
Antarctica. The highest bird
diversity occurs in tropical regions. It was earlier thought that this high diversity was the result of higher
speciation rates in the tropics, however recent studies found higher speciation rates in the high latitudes that were offset by greater
extinction rates than in the tropics. Several families of birds have adapted to life both on the world's oceans and in them, with some
seabird species coming ashore only to breed and some
penguins have been recorded diving up to .
Many bird species have established breeding populations in areas to which they've been
introduced by humans. Some of these introductions have been deliberate; the
Ring-necked Pheasant, for example, has been introduced around the world as a
game bird. Others have been accidental, such as the establishment of wild
Monk Parakeets in several North American cities after their escape from captivity. Some species, including
Cattle Egret,
Yellow-headed Caracara and
Galah, have
spread naturally far beyond their original ranges as agricultural practices created suitable new habitat.
Anatomy
Compared with other vertebrates, birds have a
body plan that shows many unusual adaptations, mostly to facilitate
flight.
The skeleton consists of very lightweight bones. They have large air-filled cavities (called pneumatic cavities) which connect with the
respiratory system. The skull bones are fused and don't show
cranial sutures. The
orbits are large and separated by a bony
septum. The
spine has cervical, thoracic, lumbar and caudal regions with the number of cervical (neck) vertebrae highly variable and especially flexible, but movement is reduced in the anterior thoracic vertebrae and absent in the later vertebrae. The last few are fused with the
pelvis to form the
synsacrum.
Like the
reptiles, birds are primarily uricotelic, that is, their
kidneys extract nitrogenous wastes from their bloodstream and excrete it as
uric acid instead of
urea or
ammonia. Uric acid is excreted along with feces as a semisolid waste since birds don't have a separate bladder or uretral opening. However, birds such as hummingbirds can be facultatively ammonotelic, excreting most of the nitrogenous wastes as ammonia. They also excrete
creatine, rather than
creatinine like mammals. The cloaca is a multi-purpose opening: waste is expelled through it, birds mate by
joining cloaca, and females lay eggs from it. In addition, many species of birds regurgitate
pellets. The
digestive system of birds is unique, with a
crop for storage and a
gizzard that contains swallowed stones for grinding food to compensate for the lack of teeth. Most birds are highly adapted for rapid digestion to aid with flight. Some migratory birds have the additional ability to reduce parts of the intestines prior to migration.
Birds have one of the most complex
respiratory systems of all animal groups. Sound production is achieved using the
syrinx, a muscular chamber with several tympanic membranes which is situated at the lower end of the trachea, from where it separates. The bird's heart has four chambers and the right aortic arch gives rise to
systemic circulation (unlike in the mammals where the left arch is involved).
The
nervous system is large relative to the bird's size.
New World vultures and
tubenoses. The avian
visual system is usually highly developed. Water birds have special flexible lenses, allowing accommodation for vision in air and water. This allows them to perceive ultraviolet light, which is involved in courtship. Many birds show plumage patterns in ultraviolet that are invisible to the human eye; some birds whose sexes appear similar to the naked eye are distinguished by the presence of
ultraviolet reflective patches on their feathers. Male
Blue Tits have an ultraviolet reflective crown patch which is displayed in courtship by posturing and raising of their nape feathers. Ultraviolet light is also used in foraging—
kestrels have been shown to search for prey by detecting the UV reflective urine trail marks left on the ground by rodents. The eyelids of a bird are not used in blinking. Instead the eye is lubricated by the
nictitating membrane, a third eyelid that moves horizontally. The nictitating membrane also covers the eye and acts as a
contact lens in many aquatic birds. Birds with eyes on the sides of their heads have a wide
visual field, while birds with eyes on the front of their heads, such as owls, have
binocular vision and can estimate the depth of field. The avian
ear lacks external
pinnae but is covered by feathers, although in some birds, such as the
Asio,
Bubo and
Otus owls, these feathers form tufts which resemble ears. The inner ear has a
cochlea, but it isn't spiral as in mammals.
A few species are able to use chemical defenses against predators; some
Procellariiformes can eject an unpleasant
oil against an aggressor, and some species of
pitohuis from
New Guinea secrete a powerful
neurotoxin in their skin and feathers.
Birds have two sexes: male and female. Birds' sex is determined by
Z and W sex chromosomes, rather than the X and Y chromosomes seen in mammals. Males carry two Z chromosomes (ZZ), and females carry a W chromosome and a Z chromosome (WZ).
Feathers and plumage
Feathers are a feature unique to birds. They facilitate
flight, provide insulation that aids in
thermoregulation, and are used in display, camouflage, and signaling. and
sex.
Plumage is regularly
moulted; the standard plumage of a bird that has moulted after breeding is known as the "non-breeding" plumage, or – in the
Humphrey-Parkes terminology – "basic" plumage; breeding plumages or variations of the basic plumage are known under the Humphrey-Parkes system as "alternate" plumages. Moulting is annual in most species, although some may have two moults a year, and large birds of prey may moult only once every few years. Moulting patterns vary across species. Some drop and regrow wing
flight feathers, starting sequentially from the outermost feathers and progressing inwards (centripetal), while others replace feathers starting from the innermost ones (centrifugal). A small number of species, such as ducks and geese, lose all of their flight feathers at once, temporarily becoming flightless. Centripetal moults of tail feathers are seen for example in the
Phasianidae. Centrifugal moult is seen, for instance, in the tail feathers of
woodpeckers and
treecreepers, although it begins with the second innermost pair of tail-feathers and finishes with the central pair of feathers so that the bird maintains a functional climbing tail. The general pattern seen in
passerines is that the primaries are replaced outward, secondaries inward, and the tail from center outward. Before nesting, the females of most bird species gain a bare
brood patch by losing feathers close to the belly. The skin there's well supplied with blood vessels and helps the bird in incubation.
Feathers require maintenance and birds preen or groom them daily, spending an average of around 9% of their daily time on this. The bill is used to brush away foreign particles and to apply
waxy secretions from the
uropygial gland; these secretions protect the feathers' flexibility and act as an antimicrobial agent, inhibiting the growth of feather-degrading
bacteria. This may be supplemented with the secretions of
formic acid from ants, which birds receive through a behaviour known as
anting, to remove feather parasites.
Scales
The scales of birds are composed of the same keratin as beaks, claws, and spurs. They are found mainly on the toes and
metatarsus, but may be found further up on the ankle in some birds. Most bird scales don't overlap significantly, except in the cases of
kingfishers and
woodpeckers.
Bird embryos begin development with smooth skin. On the feet, the
corneum, or outermost layer, of this skin may keratinize, thicken and form scales. These
scales can be organized into;
Cancella - minute scales which are really just a thickening and hardening of the skin, crisscrossed with shallow grooves.
Reticula - small but distinct, separate, scales. Found on the lateral and medial surfaces (sides) of the chicken metatarsus.
Scutella - scales that are not quite as large as scutes, such as those found on the caudal, or hind part, of the chicken metatarsus.
Scutes - the largest scales, usually on the anterior surface of the metatarsus and dorsal surface of the toes.
The rows of scutes on the anterior of the metatarsus can be called an acrometatarsium or acrotarsium.
Feathers can be intermixed with scales on some birds' feet. Feather follicles can lie between scales or even directly beneath them, in the deeper dermis layer of the skin. In this last case, feathers may emerge directly through scales, and be encircled at the plane of emergence entirely by the keratin of the scale.
The scales of birds are thought to be homologous to those of reptiles and mammals.
Flight
Most birds can fly, which distinguishes them from almost all other vertebrates. Flight is the primary means of locomotion for most bird species and is used for breeding, feeding, and predator avoidance and escape. Birds have various adaptations for flight, including a lightweight skeleton, two large flight muscles (the pectoralis—accounting for 15% of the total mass of the bird—and the supracoracoideus), and a modified forelimb (wing) that serves as an aerofoil. Flightlessness often arises in birds on isolated islands, probably due to limited resources and the absence of land predators. Though flightless, penguins use similar musculature and movements to "fly" through the water, as do auks, shearwaters and dippers.
Behaviour
Most birds are diurnal, but some birds, such as many species of owls and nightjars, are nocturnal or crepuscular (active during twilight hours), and many coastal waders feed when the tides are appropriate, by day or night.
Diet and feeding
Birds' diets are varied and often include nectar, fruit, plants, seeds, carrion, and various small animals, including other birds. Kiwis and shorebirds with long bills probe for invertebrates; shorebirds' varied bill lengths and feeding methods result in the separation of ecological niches. Loons, diving ducks, penguins and auks pursue their prey underwater, using their wings or feet for propulsion, Geese and dabbling ducks are primarily grazers. Some species, including frigatebirds, gulls, and skuas, engage in kleptoparasitism, stealing food items from other birds. Kleptoparasitism is thought to be a supplement to food obtained by hunting, rather than a significant part of any species' diet; a study of Great Frigatebirds stealing from Masked Boobies estimated that the frigatebirds stole at most 40% of their food and on average stole only 5%. Other birds are scavengers; some of these, like vultures, are specialised carrion eaters, while others, like gulls, corvids, or other birds of prey, are opportunists.
Migration
Many bird species migrate to take advantage of global differences of seasonal temperatures, therefore optimising availability of food sources and breeding habitat. These migrations vary among the different groups. Many landbirds, shorebirds, and waterbirds undertake annual long distance migrations, usually triggered by the length of daylight as well as weather conditions. These birds are characterised by a breeding season spent in the temperate or arctic/antarctic regions and a non-breeding season in the tropical regions or opposite hemisphere. Before migration, birds substantially increase body fats and reserves and reduce the size of some of their organs. although the Bar-tailed Godwit is capable of non-stop flights of up to . Seabirds also undertake long migrations, the longest annual migration being those of Sooty Shearwaters, which nest in New Zealand and Chile and spend the northern summer feeding in the North Pacific off Japan, Alaska and California, an annual round trip of . Other seabirds disperse after breeding, travelling widely but having no set migration route. Albatrosses nesting in the Southern Ocean often undertake circumpolar trips between breeding seasons.
Some bird species undertake shorter migrations, travelling only as far as is required to avoid bad weather or obtain food. species such as the boreal finches are one such group and can commonly be found at a location in one year and absent the next. This type of migration is normally associated with food availability. Species may also travel shorter distances over part of their range, with individuals from higher latitudes travelling into the existing range of conspecifics; others undertake partial migrations, where only a fraction of the population, usually females and subdominant males, migrates. Partial migration can form a large percentage of the migration behaviour of birds in some regions; in Australia, surveys found that 44% of non-passerine birds and 32% of passerines were partially migratory. Altitudinal migration is a form of short distance migration in which birds spend the breeding season at higher altitudes elevations and move to lower ones during suboptimal conditions. It is most often triggered by temperature changes and usually occurs when the normal territories also become inhospitable due to lack of food. Some species may also be nomadic, holding no fixed territory and moving according to weather and food availability. Parrots as a family are overwhelmingly neither migratory nor sedentary but considered to either be dispersive, irruptive, nomadic or undertake small and irregular migrations.
The ability of birds to return to precise locations across vast distances has been known for some time; in an experiment conducted in the 1950s a Manx Shearwater released in Boston returned to its colony in Skomer, Wales within 13 days, a distance of . Birds navigate during migration using a variety of methods. For diurnal migrants, the sun is used to navigate by day, and a stellar compass is used at night. Birds that use the sun compensate for the changing position of the sun during the day by the use of an internal clock. These are backed up in some species by their ability to sense the Earth's geomagnetism through specialised photoreceptors.
Communication
Birds communicate using primarily visual and auditory signals. Signals can be interspecific (between species) and intraspecific (within species).
Birds sometimes use plumage to assess and assert social dominance, to display breeding condition in sexually selected species, or to make threatening displays, as in the Sunbittern's mimicry of a large predator to ward off hawks and protect young chicks. Variation in plumage also allows for the identification of birds, particularly between species. Visual communication among birds may also involve ritualised displays, which have developed from non-signalling actions such as preening, the adjustments of feather position, pecking, or other behaviour. These displays may signal aggression or submission or may contribute to the formation of pair-bonds. males' breeding success may depend on the quality of such displays.
Bird calls and songs, which are produced in the syrinx, are the major means by which birds communicate with sound. This communication can be very complex; some species can operate the two sides of the syrinx independently, allowing the simultaneous production of two different songs. bond formation, the claiming and maintenance of territories,), and the warning of other birds of potential predators, sometimes with specific information about the nature of the threat. Some birds also use mechanical sounds for auditory communication. The Coenocorypha snipes of New Zealand drive air through their feathers, woodpeckers drum territorially,
Flocking and other associations
While some birds are essentially territorial or live in small family groups, other birds may form large flocks. The principal benefits of flocking are safety in numbers and increased foraging efficiency. Costs of flocking include bullying of socially subordinate birds by more dominant birds and the reduction of feeding efficiency in certain cases.
Birds sometimes also form associations with non-avian species. Plunge-diving seabirds associate with dolphins and tuna, which push shoaling fish towards the surface. Hornbills have a mutualistic relationship with Dwarf Mongooses, in which they forage together and warn each other of nearby birds of prey and other predators.
Resting and roosting
The high metabolic rates of birds during the active part of the day is supplemented by rest at other times. Sleeping birds often use a type of sleep known as vigilant sleep, where periods of rest are interspersed with quick eye-opening 'peeks', allowing them to be sensitive to disturbances and enable rapid escape from threats. Swifts have been widely believed to be able to sleep while flying; however, this hasn't been confirmed by experimental evidence. However, there may be certain kinds of sleep which are possible even when in flight. Some birds have also demonstrated the capacity to fall into slow-wave sleep one hemisphere of the brain at a time. The birds tend to exercise this ability depending upon its position relative to the outside of the flock. This may allow the eye opposite the sleeping hemisphere to remain vigilant for predators by viewing the outer margins of the flock. This adaptation is also known from marine mammals. Communal roosting is common because it lowers the loss of body heat and decreases the risks associated with predators. Roosting sites are often chosen with regard to thermoregulation and safety.
Many sleeping birds bend their heads over their backs and tuck their bills in their back feathers, although others place their beaks among their breast feathers. Many birds rest on one leg, while some may pull up their legs into their feathers, especially in cold weather. Perching birds have a tendon locking mechanism that helps them hold on to the perch when they're asleep. Many ground birds, such as quails and pheasants, roost in trees. A few parrots of the genus Loriculus roost hanging upside down. Some hummingbirds go into a nightly state of torpor accompanied with a reduction of their metabolic rates. This physiological adaptation shows nearly a hundred other species, including owlet-nightjars, nightjars, and woodswallows. One species, the Common Poorwill, even enters a state of hibernation. Birds don't have sweat glands, but they may cool themselves by moving to shade, standing in water, panting, increasing their surface area, fluttering their throat or by using special behaviours like urohydrosis to cool themselves.
Breeding
Social systems
Ninety-five percent of bird species are socially monogamous. These species pair for at least the length of the breeding season or—in some cases—for several years or until the death of one mate. Monogamy allows for biparental care, which is especially important for species in which females require males' assistance for successful brood-rearing. Among many socially monogamous species, extra-pair copulation (infidelity) is common. Such behaviour typically occurs between dominant males and females paired with subordinate males, but may also be the result of forced copulation in ducks and other anatids. For females, possible benefits of extra-pair copulation include getting better genes for her offspring and insuring against the possibility of infertility in her mate. Males of species that engage in extra-pair copulations will closely guard their mates to ensure the parentage of the offspring that they raise.
Other mating systems, including polygyny, polyandry, polygamy, polygynandry, and promiscuity, also occur. Most displays are rather simple and involve some type of song. Some displays, however, are quite elaborate. Depending on the species, these may include wing or tail drumming, dancing, aerial flights, or communal lekking. Females are generally the ones that drive partner selection, although in the polyandrous phalaropes, this is reversed: plainer males choose brightly coloured females. Courtship feeding, billing and allopreening are commonly performed between partners, generally after the birds have paired and mated.
All birds lay amniotic eggs with hard shells made mostly of calcium carbonate.
Bird eggs are usually laid in a nest. Most species create somewhat elaborate nests, which can be cups, domes, plates, beds scrapes, mounds, or burrows. Some bird nests, however, are extremely primitive; albatross nests are no more than a scrape on the ground. Most birds build nests in sheltered, hidden areas to avoid predation, but large or colonial birds—which are more capable of defence—may build more open nests. During nest construction, some species seek out plant matter from plants with parasite-reducing toxins to improve chick survival, and feathers are often used for nest insulation. The warmth for the incubation of the eggs of megapodes comes from the sun, decaying vegetation or volcanic sources. Incubation periods range from 10 days (in woodpeckers, cuckoos and passerine birds) to over 80 days (in albatrosses and kiwis). At the other extreme, many seabirds have extended periods of parental care, the longest being that of the Great Frigatebird, whose chicks take up to six months to fledge and are fed by the parents for up to an additional 14 months.
In some species, both parents care for nestlings and fledglings; in others, such care is the responsibility of only one sex. In some species, other members of the same species—usually close relatives of the breeding pair, such as offspring from previous broods—will help with the raising of the young. Such alloparenting is particularly common among the Corvida, which includes such birds as the true crows, Australian Magpie and Fairy-wrens, but has been observed in species as different as the Rifleman and Red Kite. Among most groups of animals, male parental care is rare. In birds, however, it's quite common—more so than in any other vertebrate class.
The point at which chicks fledge varies dramatically. The chicks of the Synthliboramphus murrelets, like the Ancient Murrelet, leave the nest the night after they hatch, following their parents out to sea, where they're raised away from terrestrial predators. Some other species, such as ducks, move their chicks away from the nest at an early age. In most species, chicks leave the nest just before, or soon after, they're able to fly. The amount of parental care after fledging varies; albatross chicks leave the nest on their own and receive no further help, while other species continue some supplementary feeding after fledging. Chicks may also follow their parents during their first migration.
Brood parasites
Brood parasitism, in which an egg-layer leaves her eggs with another individual's brood, is more common among birds than any other type of organism. After a parasitic bird lays her eggs in another bird's nest, they're often accepted and raised by the host at the expense of the host's own brood. Brood parasites may be either obligate brood parasites, which must lay their eggs in the nests of other species because they're incapable of raising their own young, or non-obligate brood parasites, which sometimes lay eggs in the nests of conspecifics to increase their reproductive output even though they could have raised their own young. One hundred bird species, including honeyguides, icterids, estrildid finches and ducks, are obligate parasites, though the most famous are the cuckoos.
Ecology
Birds occupy a wide range of ecological positions. Plants and pollinating birds often coevolve, and in some cases a flower's primary pollinator is the only species capable of reaching its nectar.
Birds are often important to island ecology. Birds have frequently reached islands that mammals have not; on those islands, birds may fulfill ecological roles typically played by larger animals. For example, in New Zealand the moas were important browsers, as are the Kereru and Kokako today. Nesting seabirds may also affect the ecology of islands and surrounding seas, principally through the concentration of large quantities of guano, which may enrich the local soil and the surrounding seas.
Relationship with humans
Since birds are highly visible and common animals, humans have had a relationship with them since the dawn of man. Sometimes, these relationships are mutualistic, like the cooperative honey-gathering among honeyguides and African peoples such as the Borana. Other times, they may be commensal, as when species such as the House Sparrow have benefited from human activities. Several bird species have become commercially significant agricultural pests, and some pose an aviation hazard. Human activities can also be detrimental, and have threatened numerous bird species with extinction.
Birds can act as vectors for spreading diseases such as psittacosis, salmonellosis, campylobacteriosis, mycobacteriosis (avian tuberculosis), avian influenza (bird flu), giardiasis, and cryptosporidiosis over long distances. Some of these are zoonotic diseases that can also be transmitted to humans.
Economic importance
Domesticated birds raised for meat and eggs, called poultry, are the largest source of animal protein eaten by humans; in 2003, 76 million tons of poultry and 61 million tons of eggs were produced worldwide. Chickens account for much of human poultry consumption, though turkeys, ducks, and geese are also relatively common. Many species of birds are also hunted for meat. Bird hunting is primarily a recreational activity except in extremely undeveloped areas. The most important birds hunted in North and South America are waterfowl; other widely hunted birds include pheasants, wild turkeys, quail, doves, partridge, grouse, snipe, and woodcock. Muttonbirding is also popular in Australia and New Zealand. Though some hunting, such as that of muttonbirds, may be sustainable, hunting has led to the extinction or endangerment of dozens of species.
Other commercially valuable products from birds include feathers (especially the down of geese and ducks), which are used as insulation in clothing and bedding, and seabird feces (guano), which is a valuable source of phosphorus and nitrogen. The War of the Pacific, sometimes called the Guano War, was fought in part over the control of guano deposits.
Birds have been domesticated by humans both as pets and for practical purposes. Colourful birds, such as parrots and mynas, are bred in captivity or kept as pets, a practice that has led to the illegal trafficking of some endangered species. Falcons and cormorants have long been used for hunting and fishing, respectively. Messenger pigeons, used since at least 1 AD, remained important as recently as World War II. Today, such activities are more common either as hobbies, for entertainment and tourism, or for sports such as pigeon racing.
Amateur bird enthusiasts (called birdwatchers, twitchers or, more commonly, birders) number in the millions. Many homeowners erect bird feeders near their homes to attract various species. Bird feeding has grown into a multimillion dollar industry; for example, an estimated 75% of households in Britain provide food for birds at some point during the winter.
Religion, folklore and culture
Birds play prominent and diverse roles in folklore, religion, and popular culture. In religion, birds may serve as either messengers or priests and leaders for a deity, such as in the Make-make religion in which the Tangata manu of Easter Island served as chiefs, or as attendants, as in the case of Hugin and Munin, two Common Ravens who whispered news into the ears of the Norse god Odin. They may also serve as religious symbols, as when Jonah (Hebrew: יוֹנָה, dove) embodied the fright, passivity, mourning, and beauty traditionally associated with doves. Birds have themselves been deified, as in the case of the Common Peacock, which is perceived as Mother Earth by the Dravidians of India. Some birds have also been perceived as monsters, including the mythological Roc and the Māori's legendary Pouākai, a giant bird capable of snatching humans.
Birds have been featured in culture and art since prehistoric times, when they were represented in early cave paintings. Birds were later used in religious or symbolic art and design, such as the magnificent Peacock Throne of the Mughal and Persian emperors. With the advent of scientific interest in birds, many paintings of birds were commissioned for books. Among the most famous of these bird artists was John James Audubon, whose paintings of North American birds were a great commercial success in Europe and who later lent his name to the National Audubon Society. Birds are also important figures in poetry; for example, Homer incorporated Nightingales into his Odyssey, and Catullus used a sparrow as an erotic symbol in his Catullus 2. The relationship between an albatross and a sailor is the central theme of Samuel Taylor Coleridge's The Rime of the Ancient Mariner, which led to the use of the term as a metaphor for a 'burden'. Other English metaphors derive from birds; vulture funds and vulture investors, for instance, take their name from the scavenging vulture.
Perceptions of various bird species often vary across cultures. Owls are associated with bad luck, witchcraft, and death in parts of Africa, but are regarded as wise across much of Europe. Hoopoes were considered sacred in Ancient Egypt and symbols of virtue in Persia, but were thought of as thieves across much of Europe and harbingers of war in Scandinavia.
Conservation
Though human activities have allowed the expansion of a few species, such as the Barn Swallow and European Starling, they've caused population decreases or extinction in many other species. Over a hundred bird species have gone extinct in historical times, although the most dramatic human-caused avian extinctions, eradicating an estimated 750–1800 species, occurred during the human colonisation of Melanesian, Polynesian, and Micronesian islands. Many bird populations are declining worldwide, with 1,221 species listed as threatened by Birdlife International and the IUCN in 2007. The most commonly cited human threat to birds is habitat loss. Other threats include overhunting, accidental mortality due to structural collisions or long-line fishing bycatch, pollution (including oil spills and pesticide use), competition and predation from nonnative invasive species, and climate change. Governments and conservation groups work to protect birds, either by passing laws that preserve and restore bird habitat or by establishing captive populations for reintroductions. Such projects have produced some successes; one study estimated that conservation efforts saved 16 species of bird that would otherwise have gone extinct between 1994 and 2004, including the California Condor and Norfolk Island Green Parrot.
Further Information
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