Bird anatomy, or the physiological structure of birds' bodies, shows many unique adaptations, mostly aiding flight. Birds have a light skeletal system and light but powerful musculature which, along with circulatory and respiratory systems capable of very high metabolic rates and oxygen supply, permit the bird to fly. The development of a beak has led to evolution of a specially adapted digestive system. These anatomical specializations have earned birds their own class in the vertebrate phylum.
Birds have many bones that are hollow (pneumatized) with criss-crossing struts or trusses for structural strength. The number of hollow bones varies among species, though large gliding and soaring birds tend to have the most. Respiratory air sacs often form air pockets within the semi-hollow bones of the bird's skeleton. The bones of diving birds are often less hollow than those of non-diving species. Penguins, loons, and puffins are without pneumatized bones entirely. Flightless birds, such as ostriches and emus, have pneumatized femurs and, in the case of the emu, pneumatized cervical vertebrae.
The bird skeleton is highly adapted for flight. It is extremely lightweight but strong enough to withstand the stresses of taking off, flying, and landing. One key adaptation is the fusing of bones into single ossifications, such as the pygostyle. Because of this, birds usually have a smaller number of bones than other terrestrial vertebrates. Birds also lack teeth or even a true jaw, and instead have a beak, which is far more lightweight. The beaks of many baby birds have a projection called an egg tooth, which facilitates their exit from the amniotic egg, which falls off once it has done its job.
The vertebral column is divided into five sections of vertebrae:
The neck of a bird is composed of 13–25 cervical vertebrae enabling birds to have increased flexibility. A flexible neck allows many birds with immobile eyes to move their head more productively and center their sight on objects that are close or far in distance. Most birds have about three times as many neck vertebrae than humans, which allows for increased stability during fast movements such as flying, landing, and taking-off. The neck plays a role in head-bobbing which is present in at least 8 out of 27 orders of birds, including Columbiformes, Galliformes, and Gruiformes. Head-bobbing is an optokinetic response which stabilizes a birds surroundings as they alternate between a thrust phase and a hold phase. Head-bobbing is synchronous with the feet as the head moves in accordance with the rest of the body. Data from various studies suggest that the main reason for head-bobbing in some birds is for the stabilization of their surroundings, although it is uncertain why some but not all bird orders show head-bob.
Birds are the only vertebrates to have fused collarbones and a keeled breastbone. The keeled sternum serves as an attachment site for the muscles used in flying or swimming. Flightless birds, such as ostriches, lack a keeled sternum and have denser and heavier bones compared to birds that fly. Swimming birds have a wide sternum, walking birds have a long sternum, and flying birds have a sternum that is nearly equal in width and height.
The chest consists of the furcula (wishbone) and coracoid (collar bone), which, together with the scapula, form the pectoral girdle. The side of the chest is formed by the ribs, which meet at the sternum (mid-line of the chest).
Birds have uncinate processes on the ribs. These are hooked extensions of bone which help to strengthen the rib cage by overlapping with the rib behind them. This feature is also found in the tuatara (Sphenodon).
The skull consists of five major bones: the frontal (top of head), parietal (back of head), premaxillary and nasal (top beak), and the mandible (bottom beak). The skull of a normal bird usually weighs about 1% of the bird's total body weight. The eye occupies a considerable amount of the skull and is surrounded by a sclerotic eye-ring, a ring of tiny bones. This characteristic is also seen in reptiles.
Broadly speaking, avian skulls consist of many small, non-overlapping bones. Paedomorphosis, maintenance of the ancestral state in adults, is thought to have facilitated the evolution of the avian skull. In essence, adult bird skulls will resemble the juvenile form of their theropod dinosaur ancestors. As the avian lineage has progressed and has paedomorphosis has occurred, they have lost the postorbital bone behind the eye, the ectopterygoid at the back of the palate, and teeth. The palate structures have also become greatly altered with changes, mostly reductions, seen in the ptyergoid, palatine, and jugal bones. A reduction in the adductor chambers has also occurred  These are all conditions seen in the juvenile form of their ancestors. The premaxillary bone has also hypertrophied to form the beak while the maxilla has become diminished, as suggested by both developmental  and paleontological  studies. This expansion into the beak has occurred in tandem with the loss of a functional hand and the developmental of a point at the front of the beak that resembles a "finger". The premaxilla is also known to play a large role in feeding behaviours in fish.
The structure of the avian skull has important implications for their feeding behaviours. Birds show independent movement of the skull bones known as cranial kinesis. Cranial kinesis in birds occurs in several forms, but all of the different varieties are all made possible by the anatomy of the skull. Animals with large, overlapping bones (including the ancestors of modern birds) have akinetic (non-kinetic) skulls. For this reason it has been argued that the paedomorphic bird beak can be seen as an evolutionary innovation.
The shoulder consists of the scapula (shoulder blade), coracoid, and humerus (upper arm). The humerus joins the radius and ulna (forearm) to form the elbow. The carpus and metacarpus form the "wrist" and "hand" of the bird, and the digits are fused together. The bones in the wing are extremely light so that the bird can fly more easily.
The hips consist of the pelvis, which includes three major bones: the ilium (top of the hip), ischium (sides of hip), and pubis (front of the hip). These are fused into one (the innominate bone). Innominate bones are evolutionary significant in that they allow birds to lay eggs. They meet at the acetabulum (hip socket) and articulate with the femur, which is the first bone of the hind limb.
The upper leg consists of the femur. At the knee joint, the femur connects to the tibiotarsus (shin) and fibula (side of lower leg). The tarsometatarsus forms the upper part of the foot, digits make up the toes. The leg bones of birds are the heaviest, contributing to a low center of gravity, which aids in flight. A bird's skeleton accounts for only about 5% of its total body weight.
They have a greatly elongate tetradiate pelvis, similar to some reptiles. The hind limb has an intra-tarsal joint found also in some reptiles. There is extensive fusion of the trunk vertebrae as well as fusion with the pectoral girdle.
Birds' feet are classified as anisodactyl, zygodactyl, heterodactyl, syndactyl or pamprodactyl. Anisodactyl is the most common arrangement of digits in birds, with three toes forward and one back. This is common in songbirds and other perching birds, as well as hunting birds like eagles, hawks, and falcons.
Syndactyly, as it occurs in birds, is like anisodactyly, except that the third and fourth toes (the outer and middle forward-pointing toes), or three toes, are fused together, as in the belted kingfisher Ceryle alcyon. This is characteristic of Coraciiformes (kingfishers, bee-eaters, rollers, etc.).
Zygodactyl (from Greek ζυγον, a yoke) feet have two toes facing forward (digits two and three) and two back (digits one and four). This arrangement is most common in arboreal species, particularly those that climb tree trunks or clamber through foliage. Zygodactyly occurs in the parrots, woodpeckers (including flickers), cuckoos (including roadrunners), and some owls. Zygodactyl tracks have been found dating to 120–110 Ma (early Cretaceous), 50 million years before the first identified zygodactyl fossils.
Heterodactyly is like zygodactyly, except that digits three and four point forward and digits one and two point back. This is found only in trogons, while pamprodactyl is an arrangement in which all four toes may point forward, or birds may rotate the outer two toes backward. It is a characteristic of swifts (Apodidae).
Most birds have approximately 175 different muscles, mainly controlling the wings, skin, and legs. Overall, the muscle mass of birds is concentrated ventrally. The largest muscles in the bird are the pectorals, or the pectoralis major, which control the wings and make up about 15–25% of a flighted bird's body weight.They provide the powerful wing stroke essential for flight. The muscle deep to (underneath) the pectorals is the supracoracoideus, or the pectoralis minor. It raises the wing between wingbeats. Both muscle groups attach to the keel of the sternum. This is remarkable, because other vertebrates have the muscles to raise the upper limbs generally attached to areas on the back of the spine. The supracoracoideus and the pectorals together make up about 25–40% of the bird's full body weight. Caudal to the pectorals and supracoracoides are the internal and external obliques which compress the abdomen. Additionally, there are other abdominal muscles present that expand and contract the chest, and hold the ribcage. The muscles of the wing, as seen in the labelled images, function mainly in extending or flexing the elbow, moving the wing as a whole or in extending or flexing particular digits. These muscles work to adjust the wings for flight and all other actions. Muscle composition does vary between species and even within families.
Birds have unique necks which are elongated with complex musculature as it must allow for the head to perform functions other animals may utilize pectoral limbs for.
The skin muscles help a bird in its flight by adjusting the feathers, which are attached to the skin muscle and help the bird in its flight maneuvers as well as aiding in mating rituals.
There are only a few muscles in the trunk and the tail, but they are very strong and are essential for the bird. These include the lateralis caudae and the levator caudae which control movement of the tail and the spreading of rectrices, giving the tail a larger surface area which helps keep the bird in the air as well as aiding in turning.
Muscle composition and adaptation differ by theories of muscle adaptation in whether evolution of flight came from flapping or gliding first.
The scales of birds are composed of keratin, like beaks, claws, and spurs. They are found mainly on the toes and tarsi (lower leg of birds), usually up to the tibio-tarsal joint, but may be found further up the legs in some birds. In many of the eagles and owls the legs are feathered down to (but not including) their toes. Most bird scales do not overlap significantly, except in the cases of kingfishers and woodpeckers. The scales and scutes of birds were originally thought to be homologous to those of reptiles; however, more recent research suggests that scales in birds re-evolved after the evolution of feathers.
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;
The rows of scutes on the anterior of the metatarsus can be called an "acrometatarsium" or "acrotarsium".
Reticula are located on the lateral and medial surfaces (sides) of the foot and were originally thought to be separate scales. However, histological and evolutionary developmental work in this area revealed that these structures lack beta-keratin (a hallmark of reptilian scales) and are entirely composed of alpha-keratin. This, along with their unique structure, has led to the suggestion that these are actually feather buds that were arrested early in development.
The bills of many waders have Herbst corpuscles which help them find prey hidden under wet sand, by detecting minute pressure differences in the water. All extant birds can move the parts of the upper jaw relative to the brain case. However this is more prominent in some birds and can be readily detected in parrots.
The scaly covering present on the foot of the birds is called podotheca.
The beak, bill, or rostrum is an external anatomical structure of birds which is used for eating and for grooming, manipulating objects, killing prey, fighting, probing for food, courtship and feeding young. Although beaks vary significantly in size, shape and color, they share a similar underlying structure. Two bony projections—the upper and lower mandibles—covered with a thin keratinized layer of epidermis known as the rhamphotheca. In most species, two holes known as nares lead to the respiratory system.
Although birds have lungs, theirs are fairly rigid structures that do not expand and contract as they do in mammals, reptiles and many amphibians. Instead, the structures that act as the bellows that ventilate the lungs are the air sacs, which are distributed throughout much of the birds' bodies. The airsacs move air uniderectionally through the parabronchi of the rigid lungs. Although bird lungs are smaller than those of mammals of comparable size, the air sacs account for 15% of the total body volume, whereas in mammals, the alveoli, which act as the bellows, constitute only 7% of the total body volume. The walls of the air sacs do not have a good blood supply and so do not play a direct role in gas exchange.
Birds lack a diaphragm, and therefore use their intercostal and abdominal muscles to expand and contract their entire thoraco-abdominal cavities, thus rhythmically changing the volumes of all their air sacs in unison (illustration on the right). The active phase of respiration in birds is exhalation, requiring contraction of their muscles of respiration. Relaxation of these muscles causes inhalation.
Three distinct sets of organs perform respiration — the anterior air sacs (interclavicular, cervicals, and anterior thoracics), the lungs, and the posterior air sacs (posterior thoracics and abdominals). Typically there are nine air sacs within the system; however, that number can range between seven and twelve, depending on the species of bird. Passerines possess seven air sacs, as the clavicular air sacs may interconnect or be fused with the anterior thoracic sacs.
During inhalation, environmental air initially enters the bird through the nostrils from where it is heated, humidified, and filtered in the nasal passages and upper parts of the trachea. From there, the air enters the lower trachea and continues to just beyond the syrinx, at which point the trachea branches into two primary bronchi, going to the two lungs. The primary bronchi enter the lungs to become the intrapulmonary bronchi, which give off a set of parallel branches called ventrobronchi and, a little further on, an equivalent set of dorsobronchi. The ends of the intrapulmonary bronchi discharge air into the posterior air sacs at the caudal end of the bird. Each pair of dorso-ventrobronchi is connected by a large number of parallel microscopic air capillaries (or parabronchi) where gas exchange occurs. As the bird inhales, tracheal air flows through the intrapulmonary bronchi into the posterior air sacs, as well as into the dorsobronchi (but not into the ventrobronchi whose openings into the intrapulmonary bronchi were previously believed to be tightly closed during inhalation. However, more recent studies have shown that the aerodynamics of the bronchial architecture directs the inhaled air away from the openings of the ventrobronchi, into the continuation of the intrapulmonary bronchus towards the dorsobronchi and posterior air sacs). From the dorsobronchi the air flows through the parabronchi (and therefore the gas exchanger) to the ventrobronchi from where the air can only escape into the expanding anterior air sacs. So, during inhalation, both the posterior and anterior air sacs expand, the posterior air sacs filling with fresh inhaled air, while the anterior air sacs fill with "spent" (oxygen-poor) air that has just passed through the lungs.
During exhalation the intrapulmonary bronchi were believed to be tightly constricted between the region where the ventrobronchi branch off and the region where the dorsobronchi branch off. But it is now believed that more intricate aerodynamic features have the same effect. The contracting posterior air sacs can therefore only empty into the dorsobronchi. From there the fresh air from the posterior air sacs flows through the parabronchi (in the same direction as occurred during inhalation) into ventrobronchi. The air passages connecting the ventrobronchi and anterior air sacs to the intrapulmonary bronchi open up during exhalation, thus allowing oxygen-poor air from these two organs to escape via the trachea to the exterior. Oxygenated air therefore flows constantly (during the entire breathing cycle) in a single direction through the parabronchi.
The blood flow through the bird lung is at right angles to the flow of air through the parabronchi, forming a cross-current flow exchange system (see illustration on the left). The partial pressure of oxygen in the parabronchi declines along their lengths as O2 diffuses into the blood. The blood capillaries leaving the exchanger near the entrance of airflow take up more O2 than do the capillaries leaving near the exit end of the parabronchi. When the contents of all capillaries mix, the final partial pressure of oxygen of the mixed pulmonary venous blood is higher than that of the exhaled air, but is nevertheless less than half that of the inhaled air, thus achieving roughly the same systemic arterial blood partial pressure of oxygen as mammals do with their bellows-type lungs.
The trachea is an area of dead space: the oxygen-poor air it contains at the end of exhalation is the first air to re-enter the posterior air sacs and lungs. In comparison to the mammalian respiratory tract, the dead space volume in a bird is, on average, 4.5 times greater than it is in mammals of the same size. Birds with long necks will inevitably have long tracheae, and must therefore take deeper breaths than mammals do to make allowances for their greater dead space volumes. In some birds (e.g. the whooper swan, Cygnus cygnus, the white spoonbill, Platalea leucorodia, the whooping crane, Grus americana, and the helmeted curassow, Pauxi pauxi) the trachea, which some cranes can be 1.5 m long, is coiled back and forth within the body, drastically increasing the dead space ventilation. The purpose of this extraordinary feature is unknown.
Air passes unidirectionally through the lungs during both exhalation and inspiration, causing, except for the oxygen-poor dead space air left in the trachea after exhalation and breathed in at the beginning of inhalation, little to no mixing of new oxygen-rich air with spent oxygen-poor air (as occurs in mammalian lungs), changing only (from oxygen-rich to oxygen-poor) as it moves (unidirectionally) through the parabronchi.
Avian lungs do not have alveoli as mammalian lungs do. Instead they contain millions of narrow passages known as parabronchi, connecting the dorsobronchi to the ventrobronchi at either ends of the lungs. Air flows anteriorly (caudal to cranial) through the parallel parabronchi. These parabronchi have honeycombed walls. The cells of the honeycomb are dead-end air vesicles, called atria, which project radially from the parabronchi. The atria are the site of gas exchange by simple diffusion. The blood flow around the parabronchi (and their atria), forms a cross-current gas exchanger (see diagram on the left).
All species of birds with the exception of the penguin, have a small region of their lungs devoted to "neopulmonic parabronchi". This unorganized network of microscopic tubes branches off from the posterior air sacs, and open haphazardly into both the dorso- and ventrobronchi, as well as directly into the intrapulmonary bronchi. Unlike the parabronchi, in which the air moves unidirectionally, the air flow in the neopulmonic parabronchi is bidirectional. The neopulmonic parabronchi never make up more than 25% of the total gas exchange surface of birds.
The syrinx is the sound-producing vocal organ of birds, located at the base of a bird's trachea. As with the mammalian larynx, sound is produced by the vibration of air flowing across the organ. The syrinx enables some species of birds to produce extremely complex vocalizations, even mimicking human speech. In some songbirds, the syrinx can produce more than one sound at a time.
Birds have a four-chambered heart, in common with mammals, and some reptiles (mainly the crocodilia). This adaptation allows for an efficient nutrient and oxygen transport throughout the body, providing birds with energy to fly and maintain high levels of activity. A ruby-throated hummingbird's heart beats up to 1200 times per minute (about 20 beats per second).
Many birds possess a muscular pouch along the esophagus called a crop. The crop functions to both soften food and regulate its flow through the system by storing it temporarily. The size and shape of the crop is quite variable among the birds. Members of the family Columbidae, such as pigeons, produce a nutritious crop milk which is fed to their young by regurgitation.
The avian stomach is composed of two organs, the proventriculus and the gizzard that work together during digestion. The proventriculus is a rod shaped tube, which is found between the esophagus and the gizzard, that secretes hydrochloric acid and pepsinogen into the digestive tract. The acid converts the inactive pepsinogen into the active proteolytic enzyme, pepsin, which breaks down specific peptide bonds found in proteins, to produce a set of peptides, which are amino acid chains that are shorter than the original dietary protein. The gastric juices (hydrochloric acid and pepsinogen) are mixed with the stomach contents through the muscular contractions of the gizzard.
The gizzard is composed of four muscular bands that rotate and crush food by shifting the food from one area to the next within the gizzard. The gizzard of some species of herbivorous birds, like turkey and quails, contains small pieces of grit or stone called gastroliths that are swallowed by the bird to aid in the grinding process, serving the function of teeth. The use of gizzard stones is a similarity found between birds and dinosaurs, which left gastroliths as trace fossils.
The partially digested and pulverized gizzard contents, now called a bolus, are passed into the intestine, where pancreatic and intestinal enzymes complete the digestion of the digestible food. The digestion products are then absorbed through the intestinal mucosa into the blood. The intestine ends via the large intestine in the vent or cloaca which serves as the common exit for renal and intestinal excrements as well as for the laying of eggs. However, unlike mammals, many birds do not excrete the bulky portions (roughage) of their undigested food (e.g. feathers, fur, bone fragments, and seed husks) via the cloaca, but regurgitate them as food pellets.
There are three general ways in which birds drink: using gravity itself, sucking, and by using the tongue. Fluid is also obtained from food.
Most birds are unable to swallow by the "sucking" or "pumping" action of peristalsis in their esophagus (as humans do), and drink by repeatedly raising their heads after filling their mouths to allow the liquid to flow by gravity, a method usually described as "sipping" or "tipping up". The notable exception is the Columbidae; in fact, according to Konrad Lorenz in 1939:
one recognizes the order by the single behavioral characteristic, namely that in drinking the water is pumped up by peristalsis of the esophagus which occurs without exception within the order. The only other group, however, which shows the same behavior, the Pteroclidae, is placed near the doves just by this doubtlessly very old characteristic.
In addition, specialized nectar feeders like sunbirds (Nectariniidae) and hummingbirds (Trochilidae) drink by using protrusible grooved or trough-like tongues, and parrots (Psittacidae) lap up water.
Many seabirds have glands near the eyes that allow them to drink seawater. Excess salt is eliminated from the nostrils. Many desert birds get the water that they need entirely from their food. The elimination of nitrogenous wastes as uric acid reduces the physiological demand for water, as uric acid is not very toxic and thus does not need to be diluted in as much water.
Male birds have two testes which become hundreds of times larger during the breeding season to produce sperm. The testes in birds are generally asymmetric with most birds having a larger left testis. Female birds in most families have only one functional ovary (the left one), connected to an oviduct — although two ovaries are present in the embryonic stage of each female bird. Some species of birds have two functional ovaries, and the order Apterygiformes always retain both ovaries.
Most male birds have no phallus. In the males of species without a phallus, sperm is stored in the seminal glomera within the cloacal protuberance prior to copulation. During copulation, the female moves her tail to the side and the male either mounts the female from behind or in front (as in the stitchbird), or moves very close to her. The cloacae then touch, so that the sperm can enter the female's reproductive tract. This can happen very fast, sometimes in less than half a second.
The sperm is stored in the female's sperm storage tubules for a period varying from a week to more than 100 days, depending on the species. Then, eggs will be fertilized individually as they leave the ovaries, before the shell is calcified in the oviduct. After the egg is laid by the female, the embryo continues to develop in the egg outside the female body.
Many waterfowl and some other birds, such as the ostrich and turkey, possess a phallus. This appears to be the primitive condition among birds, most birds have lost the phallus. The length is thought to be related to sperm competition in species that usually mate many times in a breeding season; sperm deposited closer to the ovaries is more likely to achieve fertilization. The longer and more complicated phalli tend to occur in waterfowl whose females have unusual anatomical features of the vagina (such as dead end sacs and clockwise coils). These vaginal structures may be used to prevent penetration by the male phallus (which coils counter-clockwise). In these species, copulation is often violent and female co-operation is not required; the female ability to prevent fertilization may allow the female to choose the father for her offspring. When not copulating, the phallus is hidden within the proctodeum compartment within the cloaca, just inside the vent.
After the eggs hatch, parents provide varying degrees of care in terms of food and protection. Precocial birds can care for themselves independently within minutes of hatching; altricial hatchlings are helpless, blind, and naked, and require extended parental care. The chicks of many ground-nesting birds such as partridges and waders are often able to run virtually immediately after hatching; such birds are referred to as nidifugous. The young of hole-nesters though, are often totally incapable of unassisted survival. The process whereby a chick acquires feathers until it can fly is called "fledging".
Some birds, such as pigeons, geese, and red-crowned cranes, remain with their mates for life and may produce offspring on a regular basis.
Avian kidneys function in almost the same way as the more extensively studied mammalian kidney, but with a few important adaptations; while much of the anatomy remains unchanged in design, some important modifications have occurred during their evolution. A bird has paired kidneys which are connected to the lower gastrointestinal tract through the ureters. Depending on the bird species, the cortex makes up around 71-80% of the kidney's mass, while the medulla is much smaller at about 5-15% of the mass. Blood vessels and other tubes make up the remaining mass. Unique to birds is the presence of two different types of nephrons (the functional unit of the kidney) both reptilian-like nephrons located in the cortex and mammalian-like nephrons located in the medulla. Reptilian nephrons are more abundant but lack the distinctive loops of Henle seen in mammals. The urine collected by the kidney is emptied into the cloaca through the ureters and then to the colon by reverse peristalsis.
Birds have acute eyesight—raptors (birds of prey) have vision eight times sharper than humans—thanks to higher densities of photoreceptors in the retina (up to 1,000,000 per square mm in Buteos, compared to 200,000 for humans), a high number of neurons in the optic nerves, a second set of eye muscles not found in other animals, and, in some cases, an indented fovea which magnifies the central part of the visual field. Many species, including hummingbirds and albatrosses, have two foveas in each eye. Many birds can detect polarised light.
The avian ear is adapted to pick up on slight and rapid changes of pitch found in bird song. General avian tympanic membrane form is ovular and slightly conical. Morphological differences in the middle ear are observed between species. Ossicles within green finches, blackbirds, song thrushes, and house sparrows are proportionately shorter to those found in pheasants, Mallard ducks, and sea birds. In song birds, a syrinx allows the respective possessors to create intricate melodies and tones. The middle avian ear is made up of three semicircular canals, each ending in an ampulla and joining to connect with the macula sacculus and lagena, of which the cochlea, a straight short tube to the external ear, branches from.
Birds have a large brain to body mass ratio. This is reflected in the advanced and complex bird intelligence.
The bursa of fabricius, also known as the cloacal bursa, is a lymphoid organ which aids in the production of B lymphocytes during humoral immunity. The bursa of fabricius is present during juvenile stages but curls up, and in the sparrow is not visible after the sparrow reaches sexual maturity.
The bursa of fabricius is a circular pouch connected to the superior dorsal side of the cloaca . The bursa is composed of many folds, known as plica, which are lined by more than 10,000 follicles encompassed by connective tissue and surrounded by mesenchyme. Each follicle consists of a cortex that surrounds a medulla. The cortex houses the highly compacted B lymphocytes, whereas the medulla houses lymphocytes loosely. The medulla is separated from the lumen by the epithelium and this aids in the transport of epithelial cells into the lumen of the bursa. There are 150,000 B lymphocytes located around each follicle.
The alula , or bastard wing, (plural alulae) is a small projection on the anterior edge of the wing of modern birds and a few non-avian dinosaurs. The word is Latin and means "winglet"; it is the diminutive of ala, meaning "wing". The alula is the freely moving first digit, a bird's "thumb", and typically bears three to five small flight feathers, with the exact number depending on the species. There also are minor covert feathers overlying the flight feathers. Like the larger flight feathers found on the wing's trailing edge, these alula feathers are asymmetrical, with the shaft running closer to anterior edge.Cloaca
In animal anatomy, a cloaca kloh-AY-kə (plural cloacae kloh-AY-see or kloh-AY-kee) is the posterior orifice that serves as the only opening for the digestive, reproductive, and urinary tracts (if present) of many vertebrate animals, opening at the vent. All amphibians, birds, reptiles, and a few mammals (monotremes, tenrecs, golden moles, and marsupial moles) have this orifice, from which they excrete both urine and feces; this is in contrast to most placental mammals, which have two or three separate orifices for evacuation. Excretory openings with analogous purpose in some invertebrates are also sometimes referred to as cloacae. Mating by cloaca is known as cloacal copulation, mostly referred to as cloacal kiss.
The cloacal region is also often associated with a secretory organ, the cloacal gland, which has been implicated in the scent-marking behavior of some reptiles, marsupials, amphibians, and monotremes.Comb (anatomy)
A comb is a fleshy growth or crest on the top of the head of gallinaceous birds, such as turkeys, pheasants, and domestic chickens. Its alternative name cockscomb (with several spelling variations) reflects that combs are generally larger on males than on females (a male gallinaceous bird is called a cock). There can be several fleshy protuberances on the heads and throats of gallinaceous birds, i.e. the comb, wattle, and earlobe, which collectively are called caruncles, however, in turkeys caruncle refers specifically to the fleshy nodules on the head and throat.
Chicken combs are most commonly red (but may be black or dark purple in breeds such as Silkies or Sebrights), but in other species the color may vary from light grey to deep blue or red; turkey combs can vary in color from bright red to blue.
The comb may be a reliable indicator of health or vigor and is used for mate-assessment in some poultry species.Crop (anatomy)
A crop (sometimes also called a croup or a craw, or ingluvies) is a thin-walled expanded portion of the alimentary tract used for the storage of food prior to digestion. This anatomical structure is found in a wide variety of animals. It has been found in birds, and in invertebrate animals including gastropods (snails and slugs), earthworms, leeches, and insects.Dactyly
In biology, dactyly is the arrangement of digits (fingers and toes) on the hands, feet, or sometimes wings of a tetrapod animal. It comes from the Greek word δακτυλος (dáktulos) = "finger".
Sometimes the ending "-dactylia" is used. The derived adjectives end with "-dactyl" or "-dactylous".Furcula
The furcula ("little fork" in Latin) or wishbone is a forked bone found in birds and some dinosaurs, and is formed by the fusion of the two clavicles. In birds, its primary function is in the strengthening of the thoracic skeleton to withstand the rigors of flight.Gizzard
The gizzard, also referred to as the ventriculus, gastric mill, and gigerium, is an organ found in the digestive tract of some animals, including archosaurs (pterosaurs, crocodiles, alligators, dinosaurs, and birds), earthworms, some gastropods, some fish, and some crustaceans. This specialized stomach constructed of thick muscular walls is used for grinding up food, often aided by particles of stone or grit. In certain insects and molluscs, the gizzard features chitinous plates or teeth.Gular skin
Gular skin (throat skin), in ornithology, is an area of featherless skin on birds that joins the lower mandible of the beak (or bill) to the bird's neck. Other vertebrate taxa may have a comparable anatomical structure that is referred to as either a gular sac, throat sac, vocal sac or gular fold.Jugal bone
The jugal is a skull bone found in most reptiles, amphibians and birds. In mammals, the jugal is often called the malar or Zygomatic. It is connected to the quadratojugal and maxilla, as well as other bones, which may vary by species.Keel (bird anatomy)
A keel or carina (plural carinae) in bird anatomy is an extension of the sternum (breastbone) which runs axially along the midline of the sternum and extends outward, perpendicular to the plane of the ribs. The keel provides an anchor to which a bird's wing muscles attach, thereby providing adequate leverage for flight. Keels do not exist on all birds; in particular, some flightless birds lack a keel structure.
Historically, the presence or absence of a pronounced keel structure was used as a broad classification of birds into two orders: Carinatae (from carina, "keel"), having a pronounced keel; and ratites (from ratis, "raft" — referring to the flatness of the sternum), having a subtle keel structure or lacking one entirely. However, this classification has fallen into disuse as evolutionary studies have shown that many flightless birds have evolved from flighted birds.Lore (anatomy)
The lore (adj. loreal) is the region between the eyes and nostrils of birds, reptiles, and amphibians.Patagium
The patagium (plural: patagia) is a membranous structure that assists an animal in gliding or flight. The structure is found in living and extinct groups of animals including bats, birds, some dromaeosaurs, pterosaurs, gliding mammals, some flying lizards, and flying frogs.Rump (animal)
The rump or croup, in the external morphology of an animal, is the portion of the posterior dorsum – that is, posterior to the loins and anterior to the tail. Anatomically, the rump corresponds to the sacrum.
The tailhead or dock is the beginning of the tail, where the tail joins the rump. It is known also as the base or root of the tail, and corresponds to the human sacrococcygeal symphysis. In some mammals the tail may be said to consist of the tailbone (meaning the bony column, muscles, and skin) and the skirt (meaning the long hairs growing from the tailbone). In birds, similarly, the tail consists of tailbone and tailfan (tail fan).
Some animals are subjected to docking, the amputation of the tailbone at or near the dock. These include dogs, cats, sheep, pigs, and horses. Humans have a remnant tail, the coccyx, and the human equivalent of docking is coccygectomy.Syrinx (bird anatomy)
The syrinx (Greek σύριγξ for pan pipes) is the vocal organ of birds. Located at the base of a bird's trachea, it produces sounds without the vocal folds of mammals. The sound is produced by vibrations of some or all of the membrana tympaniformis (the walls of the syrinx) and the pessulus, caused by air flowing through the syrinx. This sets up a self-oscillating system that modulates the airflow creating the sound. The muscles modulate the sound shape by changing the tension of the membranes and the bronchial openings. The syrinx enables some species of birds (such as parrots, crows, and mynas) to mimic human speech. Unlike the larynx of mammals, the syrinx is located where the trachea forks into the lungs. Birds also have a larynx (or cranial larynx as the syrinx is sometimes referred to as the caudal larynx) at the upper end of the trachea. Thus, lateralization of bird song is possible, with muscles on the left and right branch modulating vibrations independently so that some songbirds can produce more than one sound at a time. Some species of birds, such as New World vultures, lack a syrinx and communicate through throaty hisses.
The position of the syrinx, structure and musculature varies widely across bird groups. In some groups the syrinx covers the lower end of the trachea and the upper parts of the bronchi in which case the syrinx is said to be tracheobronchial, the most frequent form and the one found in all songbirds. The syrinx may be restricted to the bronchi as in some non-passerines, notably the owls, cuckoos and nightjars. The syrinx may also be restricted to the trachea and this is found in a very small number of bird groups that are sometimes known as tracheophonae, a subset of the suboscine passeriformes that include Furnariidae (ovenbirds), Dendrocolaptidae (woodcreepers), Formicariidae (ground antbirds), Thamnophilidae (typical antbirds), Rhinocryptidae (tapaculos), and Conopophagidae (gnateaters). The trachea are covered in partly ossified rings known as tracheal rings. Tracheal rings tend to be complete, while the bronchial rings are C shaped and the unossified part has smooth muscles running along them. The trachea are usual circular or oval in cross section in most birds but are flattened in ibises. The trachea is simple and tubular in ducks. The last few tracheal rings and the first few bronchial rings may fuse to form what is called the tympanic box. At the base of the trachea and at the joint of the bronchi a median dorsoventral structure, the pessulus, may be developed to varying extents. The pessulus is bony in passerines and provides attachment to membranes, anteriorly to the semilunar membranes. The membrane that forms part of the first three bronchial rings is responsible for vibrating and producing the sound in most passerines. These membranes may also be attached to the pessulus. In some species like the hill-myna, Gracula religiosa, there is wide gap between the second and third bronchial semirings where large muscles are attached, allowing the inner diameter to be varied widely. Other muscles are also involved in syringeal control, these can be intrinsic or extrinsic depending on whether they are within the syrinx or attached externally. The extrinsic muscles include the sternotrachealis from the sternum.Tarsometatarsus
The tarsometatarsus is a bone that is only found in the lower leg of birds and some non-avian dinosaurs. It is formed from the fusion of several bones found in other types of animals, and homologous to the mammalian tarsus (ankle bones) and metatarsal bones (foot). Despite this, the tarsometatarsus of birds is often referred to as just the tarsus or metatarsus.
Tarsometatarsal fusion occurred in several ways and extents throughout bird evolution. Specifically, in Neornithes (modern birds), although the bones are joined along their entire length, the fusion is most thorough at the distal (metatarsal) end. In the Enantiornithes, a group of Mesozoic avialans, the fusion was complete at the proximal (tarsal) end, but the distal metatarsi were still partially distinct.
While these fused bones are best known from birds and their relatives, avians are neither the only group nor the first to possess tarsometatarsi. In a remarkable case of parallel evolution, they were also present in the Heterodontosauridae, a group of tiny ornithischian dinosaurs quite unrelated to birds. The oldest remains of this taxon date from the Late Triassic more than 200 million years ago, and predate the first birds with tarsometatarsi by nearly 100 million years.Tibiotarsus
The tibiotarsus is the large bone between the femur and the tarsometatarsus in the leg of a bird. It is the fusion of the proximal part of the tarsus with the tibia.
A similar structure also occurred in the Mesozoic Heterodontosauridae. These small ornithischian dinosaurs were unrelated to birds and the similarity of their foot bones is best explained by convergent evolution.Wattle (anatomy)
A wattle is a fleshy caruncle hanging from various parts of the head or neck in several groups of birds and mammals. A caruncle is defined as 'A small, fleshy excrescence that is a normal part of an animal's anatomy'. Within this definition, caruncles in birds include those found on the face, wattles, dewlaps, snoods and earlobes. Wattles are generally paired structures but may occur as a single structure when it is sometimes known as a dewlap. Wattles are frequently organs of sexual dimorphism. In some birds, caruncles are erectile tissue and may or may not have a feather covering.Wattles are often such a striking morphological characteristic of animals that it features in their common name. For example, the southern and northern cassowary are known as the double-wattled and single-wattled cassowary respectively and there is a breed of domestic pig known as the red wattle.Wing
A wing is a type of fin that produces lift, while moving through air or some other fluid. As such, wings have streamlined cross-sections that are subject to aerodynamic forces and act as airfoils. A wing's aerodynamic efficiency is expressed as its lift-to-drag ratio. The lift a wing generates at a given speed and angle of attack can be one to two orders of magnitude greater than the total drag on the wing. A high lift-to-drag ratio requires a significantly smaller thrust to propel the wings through the air at sufficient lift.
Lifting structures used in water, include various foils, including hydrofoils. Hydrodynamics is the governing science, rather than aerodynamics. Applications of underwater foils occur in hydroplanes, sailboats and submarines.Wing chord (biology)
Wing chord is an anatomical measurement of a bird's wing. The measurement is taken with the wing bent at a 90-degree angle, from the most prominent point of the wrist joint to the most prominent point of the longest primary feather. It is often taken as a standard measurement of the proportions of a bird and used to differentiate between species and subspecies.