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Bird migration is the regular seasonal journey undertaken by many species of birds. Bird movements include those made in response to changes in food availability, habitat or weather. These however are
usually irregular or in only one direction and are termed variously as nomadism, invasions, dispersal or irruptions. Migration is marked by its annual seasonality.[1] In contrast, birds that are
non-migratory are said to be resident or sedentary.
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General patterns
Many bird populations migrate long distances along a flyway. The most common pattern involves flying north in the
spring to breed in the temperate or Arctic summer and returning in the fall to wintering grounds in warmer regions to the south.
The primary advantage of migration is conservation of energy. The
longer days of the northern summer provide greater opportunities for breeding birds to feed their young. The extended daylight hours allow diurnal birds to produce larger clutches than those of related
non-migratory species that remain in the tropics year round. As the days shorten in autumn, the birds return to warmer regions where the available food supply varies little with the season.
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These advantages offset the high stress, physical exertion costs, and other risks of the migration. Predation can be heightened during migration; the Eleonora's Falcon which breeds on Mediterranean islands has a very
late breeding season, coordinated with the autumn passage of southbound passerine migrants, which it feeds to its young. A similar strategy is adopted by the Greater Noctule bat, which preys on nocturnal passerine
migrants. The higher concentrations of migrating birds at stopover sites make them prone to parasites and pathogens, which require a heightened immune response.
Within a species not all populations may be
migratory; this is known as "partial migration". Partial migration is very common in the southern continents; in Australia, 44% of non-passerine birds and 32% of passerine species are partially migratory.
In some species, the population at higher latitudes tends to be migratory and will often winter at lower latitude. The migrating birds bypass the latitudes where other populations may be sedentary, where suitable
wintering habitats may already be occupied. This is known as leap-frog migration. Within a population, there can also be different patterns of timing and migration based on the age groups and sex. Only the female
Chaffinches in Scandinavia migrate, with the males staying resident. This has given rise to the latter's specific name of coelebs, a bachelor.
Most migrations begin with the birds starting off in a broad
front. In some cases the migration may involve narrow belts of migration that are established as traditional routes termed as flyways. These routes typically follow mountain ranges or coastlines, and may take
advantage of updrafts and other wind patterns or avoid geographical barriers such as large stretches of open water. The specific routes may be genetically programmed or learned to varying degrees. The routes taken
on forward and return migration are often different.
Many of the larger birds fly in flocks. Flying in flocks helps in reducing the energy needed. Many large birds fly in a V-formation, which helps
individuals save 12–20 % of the energy they would need to fly alone. Red Knots Calidris canutus and Dunlins Calidris alpina were found in radar studies to fly 5 km per hour faster in flocks than when they were
flying alone.
The altitude at which birds fly during migration varies. An expedition to Mt. Everest found skeletons of Pintail and Black-tailed Godwit at 5000 m (16,400 ft) on the Khumbu Glacier. Bar-headed
Geese have been seen flying over the highest peaks of the Himalayas above 8000 m (29000 ft) even when low passes of 3000 m (10000 ft) were nearby. Seabirds fly low over water but gain altitude when crossing land,
and the reverse pattern is seen in landbirds.[12][13] However most bird migration is in the range of 150 m (500 ft) to 600 m (2000 ft). Bird-hit aviation records from the United States show most collisions occur
below 600 m (2000 ft) and almost none above 1800 m (6000 ft).
In contrast, most species of penguin migrate by swimming. These routes can cover over 1000 km. Blue Grouse Dendragapus obscurus perform
altitudinal migration mostly by walking. Emus in Australia have been observed to undertake long-distance movements on foot during droughts.
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Historical views
The earliest recorded observations of bird migration were 3000 years ago, as noted by Hesiod, Homer, Herodotus, Aristotle and
others. The Bible also notes migrations, as in the Book of Job (39:26), where the inquiry is made: "Doth the hawk fly by Thy wisdom and stretch her wings toward the south?" The author of Jeremiah (8:7)
wrote: "The stork in the heavens knoweth her appointed time; and the turtledove, and the crane, and the swallow, observe the time of their coming."
Aristotle noted that cranes traveled from the
steppes of Scythia to marshes at the headwaters of the Nile. Pliny the Elder, in his Historia Naturalis, repeats Aristotle's observations. Aristotle however suggested that swallows and other birds hibernated. This
belief persisted as late as 1878, when Elliott Coues listed the titles of no less than 182 papers dealing with the hibernation of swallows. It was not until early in the nineteenth century that migration as an
explanation for the winter disappearance of birds from northern climes was accepted.[15]
The discovery in Germany of white storks embedded with African arrows provided early clues on migration. One of the
oldest of these Pfeilstorch specimens was found in 1822 near the German village of Klütz, in the state of Mecklenburg-Vorpommern.
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help of responses to environmental cues. The ability to successfully perform long-distance migrations can probably only be fully explained with an accounting for the cognitive ability of the birds to recognize
habitats and form mental maps. Satellite tracking of day migrating raptors such as Ospreys and Honey Buzzards has shown that older individuals are better at making corrections for wind drift.
As the
circannual patterns indicate, there is a strong genetic component to migration in terms of timing and route, but this may be modified by environmental influences. An interesting example where a change of migration
route has occurred because of such a geographical barrier is the trend for some Blackcaps in central Europe to migrate west and winter in Britain rather than cross the Alps.
Migratory birds may use two
electromagnetic tools to find their destinations: one that is entirely innate and another that relies on experience. A young bird on its first migration flies in the correct direction according to the Earth's
magnetic field, but does not know how far the journey will be. It does this through a radical pair mechanism whereby chemical reactions in special photo pigments sensitive to long wavelengths are affected by the
field. Note that although this only works during daylight hours, it does not use the position of the sun in any way. At this stage the bird is similar to a boy scout with a compass but no map, until it grows
accustomed to the journey and can put its other facilities to use. With experience they learn various landmarks and this "mapping" is done by magnetites in the trigeminal system, which tell the bird how
strong the field is. Because birds migrate between northern and southern regions, the magnetic field strengths at different latitudes let it interpret the radical pair mechanism more accurately and let it know when
it has reached its destination. More recent research has found a neural connection between the eye and "Cluster N", the part of the forebrain that is active during migrational orientation, suggesting that
birds may actually be able to see the magnetic field of the earth.
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