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Long-legged buzzard

The long-legged buzzard is a bird of prey found widely in several parts of Eurasia and in North Africa. This species ranges from Southeastern Europe down to East Africa to the northern part of the Indian subcontinent. The long-legged buzzard is a member of the genus Buteo, being one of the larger species therein. This species is simultaneously considered relatively powerful and aggressive for its taxonomic group as well as a relatively sluggish raptor overall. Like most buzzards, it prefers small mammals such as rodents, including gerbils, ground squirrels, voles and rats, also taking reptiles, birds and insects as well as carrion. Adaptable to a variety of habitats, long-legged buzzards may nest on a variety of surfaces, including rocks, cliffs and trees. It is a typical buzzard in its reproductive biology. The long-legged buzzard is widely distributed and appears to be quite stable in population. Therefore, it is considered as Least Concern by the IUCN.

Description
in Rajasthan, India Form and colouring This is a large and fairly sturdy Buteo. The long-legged buzzard possesses a relatively large bill on a smallish head, long wings and a rather long tail and relatively long legs with powerful feet. The species tends to be considered sluggish, perching openly and prominently and in rather upright positions on a rock, crag or similar vantage point with a good commanding view; they will also perch regularly on artificial raised points such as pylons or utility poles. Meanwhile, the intermediate adult are similar to pale adult but with somewhat richer colour, darker and more rufous upperparts and having a slightly darker and more patterned breast. The rufous morph, arguably separate from the intermediate, is more ochracecous overall and a darker rufous on the dark parts of the plumage against the more contrasting pale head. Some rufous adult long-legged buzzards can show a greyish tail with some banding and at times a darker subterminal band. Dark morph adults are all blackish-brown to black with some whitish streaks on nape. The tail of dark morphs are grey to brown-grey with a broad subterminal band and 7 rather narrow and faint bars although many completely lack the latter bars. Juveniles of the pale, intermediate and rufous morphs are similar to the respective adults of their morphs but tend to possess neater, paler edging above, especially on the tips of the greater and median coverts. Also the juveniles are more streaky about the head and breast with tail going from pale whitish darkening outwards to grey-brown with irregular faint brown bars. Dark morph juveniles are less dark than the adult of that morph, sometimes evidencing a small paler patch on breast. The juvenile dark morph long-legged buzzard's tail pattern differs from the dark adult, generally browner than adult with 3 very broad bands and a slightly broader subterminal band but dark morph juvenile tails apparently very variable. Juvenile plumage lasts up to 2–3 years when first breeding occurs. In the flight, the whitish based orangey tail often looks all white at a distance and to stand out in its paleness against the dark rear body and the rear wings. The primary coverts and many greater coverts are blackish in adult long-legged buzzards with the greater coverts pale tipped. Adults are dark grey on the flight feathers with blackish bars radiating outwards on wingtips and on the trailing edges. The underwing coverts are usually lightly streaked with rufous in pale adults, while intermediate adult has a stronger contrast from pale head and breast to darker, browner upperbody and wing coverts, breast and wing linings. The flying rufous adult tends to look more uniform above with colours varying from ochre to tawny to darker rufous brown and to possess richer coloured darker parts, with the tail very variable in rufous morph. Dark adult in flight may appear with or without a pale nape patch. Dark morph long-legged buzzards above evidence pale bases to primaries, some less dark individuals showing slight contrast of brown-tinged wing coverts against blacker carpal areas with greyish cast to secondaries but tail more obviously pale and greyer and variable. Below dark morph adult striking contrasting from dark body and underwing coverts against pale flight feathers. Mean wingspan may be about , with wingspans surely rivaling the upland buzzard as the greatest of all Buteo. The long-legged buzzard displays the typical size sexual dimorphism in favour of females, as they may be to 15% larger and can average up to 30% heavier. The measurements of live Indian long-legged buzzards were with slighter lengths of and wingspans of . Among standard measurements, nominate subspecies males attain a wing chord of while the female attains a wing chord of . In males the tail may measure while the female may measure . In tarsal length, males may measure while females attain . In the nominate race, the culmen from the cere is in both sexes, with an average of in migrants at Eilat. Mature migrants in Eilat measured from , averaging , on the enlarged hallux-claw. Identification Paler individuals of the long-legged buzzard are typically reasonably distinctive but their highly variable plumage leads to mistaken identity. The main confusion is with the even more variable common buzzard (Buteo buteo), principally of the steppe subspecies, which breeds and migrates in often similar areas. Steppe buzzards are told apart by various features of plumage, i.e. darker head and chest with a contrasting paler breast band, fully barred and darker uppertails, less distinct carpal patch both above and below, more contrasting wing lining with median coverts paler, with the greater covert darkest. Due to much variation in plumage, steppe buzzards often not reliably distinguished and in distant sightings best told apart by their smaller size and differing proportions. The steppe buzzard is distinctly smaller, of more compact build and possess a distinctly shorter wings and tail than nominate long-legged buzzards. Furthermore, the steppe buzzard has a more pronounced head but less protruding bill and flies with faster but stiffer and less flexible beats. Furthermore, steppe buzzards tend to fly with flatter wings in a glide and less pronounced dihederal without tips pointed up. Dark morphs of the respective species are so similar that they must be told by size, proportions and flight actions. Especially hard to tell apart from the steppe buzzard is the smaller North African subspecies. In Asia the long-legged buzzard is similar to the upland buzzard, which averages slightly bigger in size but is somewhat narrower winged. Typically the upland species has a large white patch on the hand above, with a uniform looking greyish white tail (with at most 2-3 dark bars only visible at close range), darker, more earthen brown on the breast and thighs and lacks the long-legged's typical warm, rufous tones. In dark morph upland buzzards, though they may manifest some darker ground colour on under secondaries and sometimes show pale U on breast but otherwise almost identical in appearance to dark morph long-legged buzzards. The only other Buteo that can be potentially confused with the long-legged buzzard is the migrant rough-legged buzzard (Buteo lagopus) which is similar in size, proportions and flight behaviour, extending to hovering (however the rough-legged is marginally smaller in size with shorter legs and a shorter bill). The rough-legged buzzard should be told apart from the long-legged by having a distinctive white based tail with a broad dark subterminal band as well as fully feathered legs, Juvenile rough-legged buzzards lack the dark underwing diagonals of many juvenile long-legged buzzards. The long-legged buzzard is potentially confusable with other medium or large unrelated species of raptor from outside of the Buteo, including multiple species of small to mid-sized eagle and two species of honey buzzard. However, all of these usually tend to have a number of distinctive morphological, especially the proportion and shapes of their wings, head and tail and flight actions, as well as plumage features that tend to easily separate them from even the most similarly hued and sized of long-legged buzzards. Voice The long-legged buzzard's voice is not well studied nor is it believed to be particularly vocal. The species is known to sometimes calls on display but it is less vocal than common buzzard. The call is similar to the latter species but the notes are shorter and slightly higher. The long-legged buzzard's commonest call is a short mew. It is also sometimes transcribed as a kyaaah and drops in pitch at the end of the brief 0.5-0.8 second call. It is said that compared to the common buzzard, the calls of the long-legged buzzard are "less squealing" and more "gull-like". A long-legged buzzard leaving its nest in Morocco just after sunrise was said to have uttered a repeated ar note, shorter fuller and apparently lower than the comparable call of a common buzzard. ==Distribution and habitat==
Distribution and habitat
The long-legged buzzard inhabits arid areas of northern Africa, southeastern Europe, west and central Asia east to China, and down to as far as central India. The farthermost western part of their breeding range is in west Africa, in Western Sahara, extreme northern Mauritania, much of Morocco west to northern Algeria (spottily elsewhere in the nation), Tunisia and northern Libya (mainly northwestern parts). Long-legged buzzards occur accidentally in several other parts of Africa. In mainland Europe, they mainly nest in the southeastern region. Nesting long-legged buzzards have been known in eastern Hungary, central and eastern Ukraine, southern Moldova, southern and far eastern Romania, southern Serbia and more broadly in Bulgaria and somewhat so in northern Greece. Recent sightings indicate that there is a small population in the Apulian region of south-eastern Italy. Similarly, increasing records of long-legged buzzards are known in far southern Spain with the first nesting occurring in Gibraltar in 2009. The recent colonisation Europe due to the climate in southern Europe becoming more suitable for this species. Vagrant long-legged buzzards have been documented in many parts of Europe, including Finland, Denmark, the Netherlands, France, Poland, Czech Republic, Slovakia, and one record in Shetland in Great Britain on 1 September 2019. Out of Europe in the eastern Mediterranean or Asia Minor, the long-legged buzzard is one of the most continuously found and abundant breeding resident raptors, being distributed throughout all of Turkey, Cyprus, Armenia, Georgia and Azerbaijan. The range continues into southwestern Russia up to about Saratov and Orenburg. More uncommonly the breeding ranges extends into Oman, the United Arab Emirates, Yemen and Saudi Arabia. The range continues almost throughout Central Asia, residing in essentially all of Turkmenistan (including broadly along the Caspian Sea coast), Uzbekistan, all but the northern stretches of Kazakhstan, Tajikistan, Kyrgyzstan and northern and central Afghanistan. The breeding range discontinues in Northwestern China but isolated breeding was documented in the Kashmir region, perhaps straddling both Pakistan and India. During times of passage, long-legged buzzards have been seen more broadly in areas such as the Arabian Peninsula, southern Iraq, western China and northeast Africa, with those that breed in Europe, Russia and Central Asia often departing their breeding grounds for the winter. The wintering areas of migrating long-legged buzzards extend through much of lower Central Asia and the Indian subcontinent including southern Afghanistan, much of Pakistan and northern India through to Nepal, Bhutan and Bangladesh. Vagrants have been recorded to as south as Sri Lanka, northern Burma and the Andaman Islands. As a whole slightly hilly plains are ideal nesting areas. In a study in Iran, 41% of long-legged buzzards were on open plains with low vegetation, 29% on plains with somewhat taller vegetation, 12% were in mountain areas and 18% were in cultivated lands. While long-legged buzzards predominantly forage in wildlands, they are also adaptable to cultivations, pastures, village outskirts and sometimes even heavily farmed areas. Reforestation in the Judean Hills in Israel and the West Bank is increasing potential interspecific conflict for other raptors in the vicinity. ==Taxonomy and systematics==
Taxonomy and systematics
The long-legged buzzard is a member of the subfamily Buteoninae, which originated in the Americas. The genus Buteo, with nearly 30 species (one of the most diverse genera of diurnal raptors), radiated through Eurasia and Africa, relatively recently in the subfamily's evolutionary history. The most similar extant species and once thought both of as conspecific and to be part of a superspecies is the upland buzzard. The upland buzzard abuts the range of long-legged buzzards from Tarbagatay to northwestern Mongolia south to Dzungaria. Although the common buzzard is not considered closely related either, hybridisation has also been recently appearing between long-legged buzzards and common buzzards in Gibraltar, as well as in the Great Hungarian Plains. Additionally, little-known buzzards (once thought to be part of the common buzzard) living on the respective islands of Socotra and Cape Verde have been found to be more closely related to the long-legged buzzard if not necessarily conspecific. Subspecies Two subspecies are currently recognised: • Buteo rufinus rufinus: With the exceptional of Arabia and perhaps the southern Middle East, the nominate race comprises all Eurasian breeding long-legged buzzards, being distributed from The Balkans east to Mongolia and India; winters in several areas of South Asia and Africa. All prior descriptions primarily refer to the nominate subspecies This subspecies tends to be notably smaller than the nominate long-legged buzzard, however evidence indicates that B. r. cirtensis breeding in Arabia and perhaps southern Israel may be larger than the African birds of the races. Wing chord of this race measures in males and in females. Additionally, tail length measures in males and in females while tarsus length is in both sexes. This reclassification has been accepted by the Ornithological Society of the Middle East, and the Collins Bird Guide, but not by the IOC World Bird List or the Avilist. ==Migration==
Migration
While the North African race is largely sedentary some short-range dispersal, wandering occasionally to Iberia, while one moved to Senegal in October, rarely southward movements occur, such as to Burkina Faso and Lagos. The species normally reaches the Indian subcontinent by about September or October and leaves by about March. A majority of the species winter in the eastern Mediterranean, i.e. Greece, Asia Minor through Middle East and Arabia to southern Tibet and northern India, as well as elsewhere in Asia. Spring returns flights occur from late February on for about a month and a half, peaking in the 2nd half of March with even fewer typically seen at major migratory sites than in the fall. For example, only about 105 are recorded throughout an average spring in Eilat. ==Dietary biology==
Dietary biology
Although frequently described as sluggish, the long-legged buzzard appears by most accounts to be a fairly active and powerful predator. Long-legged buzzards are known to visit jungle or grass fires in order to capture displaced prey, often engaging in this along with other raptors. Scavenging for carrion is not uncommon in long-legged buzzards, having been reported extensively on dog (Canis lupus familaris) carcasses in Romania, however carrion seems to be only regularly ingested during the non-breeding season. In one of the westernmost dietary studies, in Ukraine, 450 mammalian prey remains found, with 565 total prey items (5.3% birds, 8.3% reptiles, 0.2% amphibians and 6.5% beetles). Main prey here were common vole (Microtus arvalis), averaging an estimated and constituting 48.4% of the diet by number and 12.59% of the biomass and the greater mole-rat (Spalax microphthalmus) and Podolsk mole-rat (Spalax zemni), both averaging an estimated and collectively comprising 22% of the diet by number and 49.2% of the biomass. Other important prey were speckled ground squirrels (Spermophilus suslicus) with the larger mammalian prey being very young European hare (Lepus europaeus) at and adult European hamsters (Cricetus cricetus) at , on average. Further study on the Great Hungarian Plains seems to reinforce the importance as elsewhere in eastern Europe of common voles and European hamsters in the diet of long-legged buzzards. Long-legged buzzards in northeastern Greece were found to be highly reliant on the European ground squirrel which comprised 21.2% of 268 prey items there. Most other prey were largely unidentified but included Orthoptera (10.8%) Scolopendra species (10.8%), snake sp. (8.2%), Lacerta sp. (7.83%) and common voles (7.46%). s are often the primary prey of long-legged buzzard. The long-legged buzzard population in Georgia was found to live off of very small mammals. For instance, in Kvernaki Ridge, of 223 prey items, the main prey identified to species was social vole (Microtus socialis) (at 27.35%) and house mouse (Mus musculus) (at 7.17%), followed by assorted unidentified rodents (nearly 15% of diet) and Lacerta sp. (7.17%) and Caucasian agama (Paralaudakia caucasia) (4.93%). In the uplands of Ninotsminda, 244 prey items were recorded to feed mostly on unidentified small rodents, especially voles, as well as larger European water vole (7.78%) and identified common voles (5.74%). In both study areas of Georgia, mammals comprised just over 59% of the total remains, unidentified insects comprised 18.4% and 22.5% of prey numbers, birds 6.3% and 13.5% of the diet and reptiles 16.2% and 4.52% of the diets, respectively. It appears in Armenia that their diet was very reptile based, mostly small to medium-sized lizards but even the remains of a Greek tortoise (Testudo graeca) were reported. Accompanying food studies of the long-legged buzzards were conducted in the Israeli Judean Hills. Among 1239 total prey items from 32 nests here, the primary prey appeared to be Schneider's skinks at 16.3% and starred agamas at 14.6%, with an old study finding rock doves or feral pigeons (Columbus livia) the most significant at 19.6% of 561 prey items (pigeons were 10.7% amongst the 1239 prey items). Overall the Judean Hills long-legged buzzards preferred reptiles, at 47.2% of the foods, and birds, at 32.2%, rather strongly over mammals, 18.3%, which is not unexpected in the region's semi-desert environment. The predominant prey in Jordan was reportedly the fat sand rat (Psammomys obsesus) followed by again the starred agama and generally appeared not dissimilar from the diet of the species on Cyprus. On the Arabian Peninsula, long-legged buzzards were reported to feed mostly on the largish Uromastyx lizards, but also took hares, birds, and carrion. In northern Iran's Khar Turan National Park, 34 remains seemed to be predominantly represented by unidentified hares, occasionally supplemented by birds, tortoises and smaller mammals like Meriones and Gerbillus species. In southwestern Iran, 100 estimated prey items found by combination of prey remains, pellets and video recordings. The main prey were Caucasian squirrels (Sciurus anomalus) at 29.85% by number, 39.4% by biomass (with an estimated mean weight of and mature adult agamas such as brilliant ground agamas (Trapelus agilis), large-scaled agama (Laudakia nupta) (both estimated at when taken and small-scaled agama (Paralaudakia microlepis), these three comprising 30.3% of the diet collectively and 36.5% of the prey biomass. Several snakes like spotted whipsnakes (Hemorrhois ravergieri) were also taken frequently here. A study in the Kalmykia region of Russia found that about 100 prey items of long-legged buzzards consisted of by diverse prey and less based in small mammals or lizards than other regions. The most frequent identified prey here were unidentified larks, at 18% of the diet by number and 4.7% by biomass, while very young juvenile European hare, at estimated mean of body weight, were second in number, at 9%, and primary in biomass at 21.8%. Other significant prey here were social voles, at 9% by number as well, and adult rooks (Corvus frugilegus), at a mean weight of comprising 15.7% of the biomass. In northeastern China, the diet was fairly well studied, albeit in a somewhat small study. Of 50 prey items, here great gerbils (Rhombomys opimus) led the diet at 48%, followed by Tartar sand boa (Eryx miliaris) (18%), cape hare (Lepus capensis) (6%), goitered gazelle (Gazella subgutturosa) (6%) (likely but not certainly taken to the nest as carrion) and Mongolian finch (Bucanetes mongolicus) (6%). Overall mammals made 60% of the diet, reptiles 22% and birds 18%. The diet in the Indian subcontinent is quite diverse, with prey often observed to be taken consisting of small mammals, being up to 85% of the diet, with primary prey often being Indian desert jird (Meriones hurrianae) in arid areas and voles and pikas in highland areas. Lizards are significant, especially Indian spiny-tailed lizard (Saara hardwickii) and agamas, as well as snakes and various other prey. It was documented in northeastern Greece that the two species often engaged in interspecific conflicts around the nests, with the common buzzard comprising the largest percent of aggressive interactions documented for long-legged buzzards, at 10 out of 47 such interactions. In their distribution, long-legged buzzards often share relatively open, sunny and partially arid habitats and prey extensively with a number of other raptors, from smaller, weaker harriers of about three species to larger more powerful eagles such as eastern imperial eagles (Aquila heliaca) and steppe eagle (Aquila nipalensis), as well as quite often saker falcons (Falco cherrug) It was documented that the long-legged buzzard was the most significant nest constructor for nesting saker falcons in Kazakhstan, with the falcons usually using old or alternate buzzard nests. Nesting habitat often coincides with and prey is somewhat similar to the Eurasian eagle-owl (Bubo bubo), as in Bulgaria where they can even nest in the same groves, but the much larger eagle-owl can seldom be said to compete directly given its nocturnality. Other larger raptors birds are known to occasionally hunt down long-legged buzzards as well. These have been documented to include eastern imperial eagles, steppe eagles and Bonelli's eagles (Aquila fasciata). A few raptorial birds have also turned up at different times in the diet of long-legged buzzards as well and, compared to the common buzzard, the lesser studied long-legged buzzards may be more prone to interspecific killings from the number reported despite their being relatively few prey studies. Mammalian carnivores are also known to be occasional prey for long-legged buzzards as well, including least weasels (Mustela nivalis ) and marbled polecat (Vormela peregusna) as well as, although these are more likely taken either while young or as carrion, red foxes (Vulpes vulpes) and European wildcats (Felis silvestris). ==Breeding==
Breeding
The long-legged buzzard is, as is typical for Buteo and accipitrids, usually rather solitary outside of the pair bond. However, occasionally forms very loose breeding groups, at times several as close as or in the same crag. It is also slightly gregarious sometimes in passage in small groups, rarely traveling in large flocks. Territories are fairly large for long-legged buzzards. All known nests in northwestern China as well as in southwestern Iran were located on cliffs. Additionally, the few known nests from Pakistan have appeared to be located in trees such as Abies firs or junipers. Some nests along the perimeter of old buildings have been documented as well. The average clutch size in Ukraine was 2.7, in a sample of 8. The average clutch size in North Africa was reported (in a sample of 57) as 2.54. The clutch size in northwestern Iran averaged 3. In northwestern China, the mean clutch size was 3.3. The eggs are slightly rough, oval and largely whitish with a yellowish tint and a few wart like projections, with indistinct grey-brown to reddish brown markings, which tend to fade at the pointer tip of the oval. The average egg sizes in Ukraine, Armenia and northwestern China were , and , respectively. Egg heights ranged from and diameter ranged from , while in Armenia eggs weighed on average and in China they weighed . Incubation appears to last for about 28 to 30 days. Upon hatching, the young are expectedly semi-altricial. The brood size averages about 2.3. The chicks initially have fine white down at first and then develop a second down coat with white to creamy white. The chicks are brooded considerably, especially by their mother for about 30 days, after which she may resume hunting. Fledgling of the chicks may occur at between 40 and 46 days of age for the young buzzards. The dependence period after they leave the nest can be relatively prolonged for a temperate-zone raptor, reaching perhaps a month in total. Breeding success rates are relatively quite poorly known in long-legged buzzards, with many sources failing to find extensive data on this topic. Data from Cyprus shows the nesting success varying greatly, perhaps based on food supplies, with an annual mean success rate varying from 46% to 93%. In northwestern China, the mean number of fledglings per nest was 0.7 while the mean fledged from successful nests was 1.4. The maximum estimated mean productivity per pair in Israel was about 0.96. ==Status==
Status
Some declines have been reported in western Russia and generally the long-legged buzzard may be somewhat less numerous than they once were in the more western parts of the range. The following estimates show from the smaller numbers of the 1990s to the generally higher estimated numbers by 2015. There are an estimated 800-1500 pairs nesting in western Russia, 200-750 pairs occurring in Bulgaria and about 60-300 pairs in Greece and 50 pairs in Ukraine, with fewer in Albania and a few other countries. Europe contains less than a quarter of the global population and the declines from historic numbers were still over 30%, so the long-legged buzzard is considered locally a Vulnerable species in Europe. Fewer figures still are available from Asia, where the species is considered uncommon to rare in Pakistan, slightly more common in Kashmir and variously rare to uncommon in northwestern China and Turkmenia. Good habitat and strong circumstantial evidence of strong continuous breeding pairs in Central Asia has led to a projected fairly ample but poorly documented population in this region. ==References==
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