In Thai: นกอินทรีทุ่งหญ้าสเต็ป, nok in-sree thung yaa sa-tep
Binomial name: Aquila nipalensis, Brian Houghton Hodgson, 1833
The steppe eagle (Aquila nipalensis) is a large bird of prey. Like all eagles, it belongs to the family Accipitridae. The steppe eagle’s well-feathered legs illustrate it to be a member of the subfamily Aquilinae, also known as the “booted eagles”. This species was once considered to be closely related to the non-migratory tawny eagle (Aquila rapax) and the two forms have previously been treated as conspecific. They were split based on pronounced differences in morphology and anatomy; two molecular studies, each based on a very small number of genes, indicate that the species are distinct but disagree over how closely related they are.
The steppe eagle is in many ways a peculiar species of eagle. It is a specialized predator of ground squirrels on the breeding ground, also taking other rather small mammals and other prey, doing so more often when ground squirrels are less consistently found. In rather treeless areas of the steppe habitats, these eagles tend to nest on a slightly rise, often on or near an outcrop, but may even the flat, wide-open ground, in a rather flat nest. They are the only eagle to nest primarily on the ground. Usually one to three eggs are laid and, in successful nests, one to two young eagles fledge. The steppe eagle undertakes a massive migration from essentially its entire breeding range, moving enmass past major migration flyways, especially those of the Middle East, Red Sea and the Himalayas. In winter, though less closely studied than during breeding, the steppe eagle is remarkable for its sluggish and almost passive feeding ecology, focusing on insect swarms, landfills, carrion and the semi-altricial young of assorted animals, lacking the bold and predatory demeanor of their cousin species. Although still seen by the thousands at migration sites in larger numbers than other migrating eagles of these areas, the steppe eagle’s entire population has declined precipitously. The threats to this species consist of increasing steppe fires and pests around the nests (both probably increased by the warming climate) which can cause a large volume of nest failures. Rivaling these factors, disturbance and persecution by humans and trampling by livestock are also destroying many nests. Free-flying steppe eagles are also being killed in alarmingly large numbers, especially in the stronghold nation for breeding of Kazakhstan, by electrocutions on dangerous electricial wires and pylons. Due to these and other reasons, the decline of the species is thought to be considerably in excess of 50%. Therefore, the species is considered to be endangered by the IUCN. The Steppe Eagle appears on the flag of Kazakhstan. It is also the national bird (animal) of Egypt and appears on its flag.
British naturalist Brian Houghton Hodgson described the steppe eagle in 1833. Aquila is Latin for “eagle” while nipalensis means “from Nepal” based on the location where the type specimen was collected presumably while migrating. The steppe eagle is a member of the booted eagle subfamily within the Accipitridae family. The booted eagle clan are monophyletic and study of karyotypes has indicated that they likely have few to no close external relations within the overall extant accipitrid family. The booted eagle subfamily all have feathers covering their legs and may be found to some extent on every continent that contains accipitrids. The genus Aquila is has been thought to traditionally composed of by large and fairly dark eagles that generally habituate to various open habitats. However, a significant division was determined to exist between superficially similar eagles such as the golden eagle (Aquila chrysaetos) and its three extant and similar-looking close cousins, as well as three very different smaller and pale-bellied eagles, and the species complex which contains the steppe eagle. There is a similar genetic disparity with the golden eagle for the steppe eagle as with the spotted eagles which have been deemed distinct enough to form a separate genus, Clanga. The steppe eagle genetically clusters closely to the tawny eagle as well as, albeit more distantly, with the eastern (Aquila heliaca) and Spanish imperial eagles (Aquila adalberti). However, the loci evidenced in the Aquila genera have been found to be relatively homogenous, with general studies of isoenzymes showing their genes as about ten times less distanced than certain owl genera.
The steppe eagle has historically been considered conspecific with the tawny eagle, even until as recently as 1991. The latter species resides year-around in the African and Asian areas often used seasonally as wintering grounds by steppe eagle. The species were ultimately separated on the grounds of the differences in morphology, disparate coloring, distinct life histories and behaviours. Testing of genetic materials has reinforced the species distinction of the steppe and tawny eagles. Genetically, the steppe eagle is thought to be basal to related species such as the tawny and imperial eagles. A fossil species, Aquila nipaloides, has been found in Italy, Corsica, Sardinia and France and was hypothesized to most closely related to the steppe eagle based on osteology of the ramus (although did evidence some differences in leg morphology). Despite being even more strongly distinctive from the steppe eagle than the tawny eagle, the eastern imperial eagle has been seen to hybridize with the steppe eagles in the wild, once in Turkey and at least three times in Kazakhstan. Each hybrid with imperial eagles has been known to involve pairs of subadult or juvenile eagles and all known hybrid pairings were between male steppe eagles (or apparent steppe-imperial hybrids themselves) mated to female imperial eagles. Some of these hybrid pairs also produced seemingly healthy young with roughly intermediate characteristics.
The steppe eagle has been generally considered to contain two subspecies. One was the nominate subspecies, A. n. nipalensis, which breeds in the eastern portions of the range (perhaps from the East Kazakhstan Region to all points east) while the western breeding population, found in most of Kazakhstan and European Russia, was considered as the subspecies, A. n. orientalis. The separation of two subspecies was largely based on size, with the eastern population being larger and much heavier than the western eagles. The more eastern birds tend to be a shade darker and a have a more extensive nape patch, as well as having a more conspicuously deep gape-line. However, both western and Russian researchers have since made a convincing advocacy that the steppe eagle is actually a monotypical species. It was found that both previously claimed subspecies appear to broadly overlap in the breeding range and become indistinguishable at the Kazakh-Russian meeting point. The primary differences, i.e. in size and mildly in colour, can be explained as clinal variations due to the environment. The breeding populations of the eastern and western eagles are insufficiently allopatric and too extensively engage in introgression to be properly regarded as full subspecies. Erroneously, a checklist once included the former subspecies of A. n. orientalis as being part of the subspecies of tawny eagle from Asia, A. r. vindhiana, an error that was later corrected.
The steppe eagle is a large, bulky and robust-looking eagle. It is mainly dark brown in colour with a longish but very thick neck and a relatively small head that nonetheless features a strong bill and long gape-line. It appears long-winged and has a longish and rather rounded tail and markedly well-feathered (almost with disheveled looking feathers) legs. Steppe eagles tend to perch somewhat upright and usually do so in the open, often utilizing isolated trees, posts, rocks or other suitable low lookouts such as mounds or straw-piles. The species often is seen on the ground where may stand for long periods of the day and walk with horizontal posture and with wingtips just exceed the tail-tip. Steppe eagles, like tawny eagles, can fairly tame and approachable, unlike many of the other Aquila eagles. The adult is a somewhat variable brown with darker centers to the greater coverts. More pronouncedly in the eastern part of the range, adults have normally prominent pale rufous to dull orange-yellow to yellow-brown patches on the nape and hindcrown. Any other paler areas (such as the feather tips of the back and uppertail coverts) are obscured on perched adults. The massive gape-line runs to level with the rear of eye (further emphasized by dark border against paler chin) and is longer than in any other Aquila eagles including tawny eagles. Combined with their deep-set eyes, it lends steppe eagles an altogether rather fierce facial expression. Steppe eagle juveniles are almost invariably paler than adults, with some ranging overall from umber-brown to tawny-buff but then some are darker and more deeply brown. Juveniles tend to be brown to grey-brown on the upperparts but for generally rufous-buff nape patch (more so on eastern population). The juveniles bear conspicuously and broadly white-tipped black about the greater coverts, wings and tail and a bold but narrow cream band on the brown medians. The juvenile steppe eagle’s white uppertail coverts is generally concealed when perched; the underparts are usually the same as the upperparts but may be somewhat paler tawny-buff hue. Upon their 2nd year, the plumage is still much as the 1st year appearance but show the pale tips to secondaries, median coverts and tail as often well-worn and narrower; by the start of 2nd winter the, tips of retained juvenile flight-feathers and coverts are heavily abraded and very thin. By the end of 2nd winter, often the immatures look very worn and have nearly lost pale tips altogether and from 3rd year onward manifest a variable mix of old and new feathers. Generally, immatures are often rather scruffy in appearance until adult-like plumage attained at year five, after which the feathers generally appear more compact. Adults have brown to hazel eyes, while juveniles have distinctly dark brown eyes; the cere and feet are yellow at all ages.
In flight, the steppe eagle appears as a large, impressive and visibly heavy raptor with a well-projecting large head and bill and rather broad neck and long, broad wings. They evidence proportionately long arms, especially in the larger eastern birds. The wings tend to be held almost parallel-edged and square-ended with 7 very elongated emarginations. Often juveniles can tend to appear somewhat narrower winged. The broad body of the species often looks suspended underneath and the tail appears rounded or even wedge-shaped, measuring about 3/4 of the length of wing-base. The wingspan is about 2.6 times greater than the total body length. On the upperwings, steppe eagles show a pale greyish primary patch that is often quite large and obvious (especially on non-adults), often being pale at the base on the greater primary coverts but on adults (especially dark birds) much less marked. On the underwing, a very small carpal crescent may be present but can vary from invisible to slightly more marked. The flight feathers are greyish and all have 7-8 well-spaced blackish bars (albeit less conspicuously than on spotted eagles), while the fingers are plain blackish. Adults are basically all fairly uniform dark brown (wings can be negligibly greyer or rarely yellowish brown). Adults may evidence in flight some whitish patches on back and tail coverts that are varying from insignificant to fairly prominent. Adult eagles that do show a dark-barred greyish primary patch usually have that confined to a wedge-shape on inner primaries though can sometimes be rather more prominent. Below adults show dark-barred grey flight feathers and tail with the broad blackish trail edges and wing ends being rather distinctive; the wing linings are often slightly paler to darker than remiges and often with an obscure remnant of broken paler central band. Juveniles are quite distinctive in flight if seen in reasonable view. Above, juveniles are pale greyish-brown to yellow-brown about the body and forewing-coverts, have a broad whitish U above the tail. They possess broad white tips to the blackish greater coverts, flights feathers and tail creating obvious whitish bars on the wings and trailing edges as well as a large and prominent whitish patch covering much of the inner primaries (causing barring to stand out more so and offsetting plain black wing end). On its underside, the juvenile is mid-brown to brownish-yellow with a paler throat and creamy crissum. Below, the creamy central wing band is even broader than above, while the greater coverts all white with some dark centres on primaries (rare extreme pale individuals appear to have almost uniform paler colour on the entire wing lining and lesser and medians buffish-white to pale sandy, often whitish pale primary-wedges). Despite reports that some juvenile 1st years have subtle or no central wing bands, these are believed to be cases where these feathers exist but are obscured by long median coverts. At the end of the first year, the young steppe eagle tends to have pale tips to wings, tail and upperwing coverts become rather abraded; thereafter the development young evidence much variation due to individual differences. Usually, by the end of 2nd winter, the wing looks even more worn and uneven in pattern, with any newly acquired narrowly white-tipped quills clearly longer than old worn juvenile ones that have lost their pale tips. From the 3rd winter on, the pale parts clearly reduced, flight feathers and tail often appear quite ragged and by the 4th year start to more resemble adults. From the end of the 3rd year to when they obtain adult plumage, the eagles tend to have adult-like broad blackish trailing edges and tail often coupled with dark barred grey base to black fingers and traces of the pale band along greater underwing-coverts. Maturity is obtained between the 4th and 5th years, not at 6-7 years as previously reported despite some presumed five year old eagles still have flecks of pale on the wing coverts and the throat and more subtle nape patches than they will ultimately manifest.
The steppe eagle is large and impressive raptor and quite a large eagle. However, as a member of the genus Aquila, it is fairly medium-sized. Females can range to 15% larger with greater dimorphism by weight, which is more pronouncedly dimorphic than by linear dimensions. Total length can range from 60 to 89 cm in fully-grown steppe eagles. Wingspan in full grown eagles of this species is very variable, with the smallest steppe eagles spanning as little as 165 to 174 cm ftin while the largest ones can reportedly span up to 250 to 262 cm ftin. Although some sources list the maximum wingspan as only 214 or 216 cm ftin, the maximum wing dimensions were apparently confirmed for the most massive steppe eagles (i.e. from Altai). Body mass, like wingspan, as reported is also fairly variable. Steppe eagles weighed for a Russia handbook were found to scale from 2.5 to 3.5 kg in males while in females weights reported to range from 2.3 to 4.9 kg. Elsewhere, the minimum full-grown weights for smaller western eagles (formerly subspecies A. n. orientalis) were 2 kg for the smallest males while the heaviest females were found to have attained a weight around 3.9 kg, while weights in the eastern part of the breeding range are around 20% heavier. In one sample of steppe eagles of possibly varied origins, males weighed a mean of 2.48 kg and females a mean of 3.56 kg. Wintering eagles of the species in southern Africa weighed a mean of 3.02 kg in a sample of four. In Saudi Arabia, 21 steppe eagles at one study site weighed a mean of 3.28 kg while 27 eagles at another study site there weighed a mean of 3.45 kg. Unpublished weights from Israel were much lower at a reported mean of 2.11 kg, as in other raptors during passage migration in Israel, weight loss may be significant relative to the other seasons. Steppe eagles diagnosed as from the smaller-bodied, western part of the breeding range weighed a mean of 2.46 kg in 13 males and a mean of just under 3 kg in a sample of 18 females while the mean weight of larger, eastern breeding bird was listed as 3.01 kg in 2 males and 3.57 kg in 2 females. The maximum cited weight for steppe eagle males in the wild is 4.6 kg while that for females is 5.5 kg. Among standard measurements, the wing chord can measure from 510 to 610 mm in males and from 536 to 640 mm in females. The tail may measure from 238 to 295 mm in both sexes and the tarsus may be from 85 to 96 mm in males and from 92 to 98 mm in females. Wing chord length averaged 536 mm and 566 mm in males and females in a study, respectively. The huge gape of a steppe eagle is from 49 to 60.8 mm wide, with an average of 53.1 and 55.3 mm in males and females, respectively, while the gape length is 40 to 49.7 mm, averaging 44.3 and 45.8 mm in the two sexes. The hallux claw, the enlarged killing talon on the rear foot of essentially all accipitrids measures from 28.3 to 36.8 mm, averaging 33.8 mm, in males from 31.8 to 40.5 mm, averaging 36 mm, in females.
In many circumstances, the steppe eagle can be very difficult to distinguish from other similar eagles, often especially during passage and winter. Adults are often confused with spotted eagles but are best separated by their much more broad build, far greater wing areas with longer, more rectangular or squarish wing tips and longer, more conspicuous fingers, larger head (rather than small and bull-headed) and larger overall size. Compared to the spotted eagles, the flight of the steppe eagle is more aquiline, i.e. more powerful, labored and deep while spotted eagles tend to fly more like buzzards. The lesser spotted eagle (Clanga pomarina), the most similarly marked of spotted eagles, is particularly less powerful looking with a shorter neck, much smaller wing areas, shorter fingers and tail and less extensive, baggy leg-feathering. The greater spotted eagle (Clanga clanga) is also smaller and slighter but to a reduced extent. When plumage is clear to see, steppe eagles have more clearly and more extensively barred quills and lack the clear carpal arcs of the two widespread spotted eagles but these differences are obscured at greater distances. Some subadult steppe eagles, with their paler brown wing-coverts above and below and only traces of white underwing bands and clearly pale primary patch above in particular quite resemble the plumage of older lesser spotted eagles. The white wing bars of steppe eagles are usually more conspicuous than those of the lesser spotted eagle. At close range, the steppe eagle has a deeper gape than lesser and greater spotted eagles and has rounded rather than oval nostrils. When seen perched, either on an perch or on the ground, spotted eagles of all three species tend to stand quite tall and upright, emphasizing their more slender and lightly feathered legs, while the steppe eagle sits more horizontally and is always far bulkier than even the biggest greater spotted eagles. Some particularly dark adult and subadult steppe eagles with obscured paler wing feathers can greatly resemble adult greater spotted eagles (the latter species can appear almost blackish in certain lights) and would need to be identified by the differences in size and form. The Indian spotted eagle (Clanga hastata) has a deep gape reminiscent of the steppe eagle but is much slighter in overall size, being scarcely larger than a lesser spotted eagle, and has even less conspicuous whitish wing markings than the lesser spotted. As a result of their rough similarities, many young steppe eagles are misidentified, particularly from a distance, with spotted eagles although generally identification is possible via a combination of structure and plumage features. Juvenile steppe eagles are normally readily identified by distinctive plumage features but can recall juvenile eastern imperial eagles, the latter has longer and less rounded tail, a more prominent (rather than deeply set) bill, has a much paler and more buff overall colour while the chest is overlap with brown streaking and the quills are unbarred. Imperial and steppe eagles are often similar in size, with more western breeding birds usually being somewhat smaller when seen side-by-side with an imperial eagle and the eastern steppe eagles being of similar average size (but even larger maximum size) compared to full-grown imperial eagles. Steppe eagles are told from tawny eagles by that species being smaller and less bulky with shorter wings, a smaller gape, a more slender neck and a relatively longer tail. Both the tawny and steppe eagle tend to have a distinct S-shape curvature to the trailing edge of the wings. When perched on the ground, the tawny eagle tends to stand more upright, while the steppe eagle often appears to assume a more elongated, horizontal posture. Plumage variations of tawny eagles can render them a surprisingly close colour to the usually darker, duller and browner steppe eagle (especially so in south Asia), but they never obtain the distinct whitish wing band of the young steppe eagle nor the nape patch of most adult steppes. Despite slight individual and clinal variations, the steppe eagle, unlike the tawny eagle, is not polymorphic. These aforementioned eagles present the main possibilities for confusion, less likely mistakes can potentially range from relatively dainty and much smaller Wahlberg's eagles (Hieraeetus wahlbergi) (generally quite different in features but somewhat similarly hued) in Africa to the somewhat bigger but differently structured golden eagles (much longer tail, relatively smaller bill and much smaller gape, different wing shape, more aquiline build and bigger feet and talons) in much of the range.
Breeding and wintering ranges
The steppe eagle once bred southeasternmost Ukraine and still rarely occurs as a breeder in southwest Russia from Stavropol to Astrakhan. The steppe eagle is still mapped to breed down to Makhachkala and Maykop to as far west as Leningradskaya, up north as far as the lower Volga and down to the Caspian Sea nearly as far as Makhachkala and south of Fort-Shevchenko. The breeding range can extend through appropriate habitat in northeastern Kyrgyzstan and in much of Kazakhstan, from north of Nur-Sultan south to (albeit spottily) to Kyzylorda as well as around the Aral Sea, sweeping far to the east in Transbaikal and western Tian Shan, Xinjiang, Altai, Mongolia, the Gobi area, Gansu, Ningxia, northern Tibet (by far their southernmost breeding area), Inner Mongolia and reaching their eastern breeding limits in Manchuria and elsewhere in northeastern China. The steppe eagle is entirely migratory, wintering in east and, to a lesser extent, southern Africa. Their African range can extend western to southern Sudan, almost throughout east Africa, to the easternmost part of Democratic Republic of the Congo. The southern African wintering range extends to central Angola, northern and eastern Namibia south to Botswana, Zambia, Zimbabwe, Swaziland and northern South Africa, including former Transvaal and northern Natal as well as rarely south of the Orange River In South Africa, steppe eagles are reportedly often frequent only in the lowveld of Kruger National Park area. The steppe eagle’s wintering range also extends into the Middle East. They occur broadly in the season in several central and southern parts of the Arabian Peninsula as well as regularly in eastern Iraq and western Iran with odd ones north to Turkey and Georgia. Although sometimes recorded as occurring “somewhat” in Arabia, more extensive surveying has revealed that many, if not more, steppe eagles wind up winter in the peninsula rather than Africa, and that the largest ever winter numbers were recorded in Saudi Arabia, where around 7200 individuals (or perhaps up to 9% of the current world population) were recorded near Riyadh. As many as 3000 have also been similarly recorded in the nation of Oman. Other nations to host wintering steppe eagles include Yemen, Azerbaijan and Syria as well as, albeit rarely doing so, in the United Arab Emirates, Lebanon and Kuwait.
Unusually, a few overwintering steppe eagles have been now recorded in Kazakhstan, apparently near Shymkent, in the Aksu-Zhabagly Nature Reserve, the valley of the Syr Darya, the Chardara Dam and towns of the East Kazakhstan Region. In south Asia, the species in winter may occur from Afghanistan (rarely wintering still in the Nuristan Province) and in much of the Indian subcontinent. Pakistan’s Poonch and Jhelum valleys of Azad Kashmir are known to host a mean of 154 steppe eagles per study area. In India, they may occur mainly south to Madhya Pradesh, the Indo-Gangetic Plain, the Deccan Peninsula and Himalayan zone, Mizoram, Assam and southern Orissa. Vagrants have been recorded in India to Periyar National Park, Mahendragiri, Kanyakumari Wildlife Sanctuary and Mudumalai National Park. The wintering range extends east to Tibet (although the species is said to be gone from Lhasa in recent years), Nepal, Burma and broadly in east China from southeastern Guizhou to Hainan and southwestern Guangdong. Recent wintering records reflect the species as lingering seasonally at different points of the non-breeding season, albeit very seldomly, in central and southern Myanmar, western Thailand, peninsular Malaysia and northern Vietnam. The species may have been aided in expanding their eastward wintering range by deforestation practice.
The steppe eagle appears broadly in many nations between their central Eurasian breeding areas and their generally tropical Indo and African wintering grounds. As a matter of fact, the largest concentrations of the species tend to occur at times of passage. The steppe eagle can also vagrate not infrequently far away from traditional migration sites, and has turn up in many areas from western Europe to as far east as Japan. Vagrant steppe eagles have been recorded in at least the following nations or regions: at least 6 nations in west Africa Morocco, Tunisia, the Netherlands, Finland (at least 50 times) as well as Spain and France, the Czech Republic, Bulgaria and Romania (in both of which they once bred but were extirpated), Greece Mordovia, Yakutia, the Korean Peninsula and probably down to Borneo in Asia. Migration sites include the both mountainous ridges and the larger seas along their routes. Steppe eagles predominantly use two main migration routes: one radiates across the Middle East and Arabia, with many birds stopping to winter, but many too migrate around the Red Sea to winter in Africa while the other main migration path frequently involves farther eastern breeding eagles moving along many ridges and prominent flyways before radiated across a broad path through the Himalayas, in order to reach the south Asian and other Asian wintering sites. Less known or less frequently migration paths before these well-known routes of passage may lead steppe eagles around the Black Sea in the west and, much more frequently, around the Caspian Sea farther east. Nations known to be visited by steppe eagles almost exclusively in migratory passage include Egypt, most but not all of Syria, Turkmenistan and Afghanistan and much of east China from Tuquan County to about Xiamen. Points of migration bottleneck, where large numbers of steppe eagles are frequently recorded, are known in areas including Israel, especially around Eilat, Suez (in Egypt), Bab-el-Mandeb (in Yemen), some parts of the nation of Georgia and, in the Himalayan region, especially within Nepal but also sometimes en mass in Pakistan and northern India. Migration sites of minor significance are less known but include Alborz.
The steppe eagle tends to breeds in open dry country, within the characteristic habitat it is named after: the steppe. In Kazakhstan, it is known to occur in drier parts of the steppe than some other raptors like harriers, in both upland and lowland steppe, and general avoid utilizing agricultural land such as arables and most other human-fragmented areas (but are somewhat tolerant of nesting near roads). Associated habitats are frequented when breeding such as flat plains, arid grassland, semi-desert and even desert edge. Most members of the species breed at lower levels but largely in eastern part of the range also will nest in poorly vegetated dry rocky hillsides such as granite massifs and upland valleys, though generally avoid truly mountainous areas. Wintering steppe eagles often occur much more frequently in human-modified areas in order to access easy foods. These include landfills and livestock carcass dumps, these being used frequently everywhere from Arabia to India. More natural habitats used most often by wintering steppe eagles tend to various wetlands or other waterways where they are available. In winter, mostly savanna and grasslands are the predominant habitat used in Africa, also sometimes dry woodland. Study in Botswana indicated that wintering steppe eagles there appeared to be indifferent to land use changes by humans. In Zambia and Malawi, it was found that the steppe eagle was only frequent in high-elevation plateau areas from 370 to 2400 m metres above sea level. Use of plateaus was also frequent in Zimbabwe, often where open savanna woods of Acacia stand as well as the use of cultivated areas such as wheat stubble fields by eagles. Iraqi wintering steppe eagles often used dump sites as well as deserts and semi-arid areas, with more steppe, other grassland and mountain slopes used in northern Iraq in winter. In Armenia steppe eagles are apparently frequent in old fields and orchards. In south Asia they usually use open country and often frequents large lakes and other wetlands near arid areas but may accept, or even prefer, more heavily wooded areas (however the first records from peninsular Malaysia seem to be from open areas created by deforestation). Although usually a breeder of lowlands, it has been known to live at elevations of up to 2300 m and locally to 3000 m in mountains, on passage can occur to over 4500 m sometimes even to 7925 m, as was recorded on Mount Everest. Compared to other Palearctic migrating eagles, the steppe eagle seems to perhaps be slightly more tolerant of a wider range of climatic conditions, including rather humid conditions in India provided subsistence is available as well as up to 50 cm of snow cover in Kazakhstan (living off of urban pests).
The steppe eagle is sometimes regarded as solitary but is frequently seen in the company of conspecifics throughout the year. Besides the obvious breeding pair, they often flock during migration and aggregate in occasionally ample numbers during non-breeding times, usually at fruitful feeding sites, sometimes briefly cooperating with one another especially to klepoparasitize other birds of prey. Steppe eagles fly with slow, deep and stiff-looking wing beats, holding wings fully extend on upstrokes, rendering a heavier flight pattern than spotted eagles. The flight of the steppe eagle is well-analyzed such as experiments with a captive male and observations of migrants in Israel. It appears that the underwing coverts operate as a high-lift device and probably provide stability through unsteady maneuvers, otherwise positive loading on the wings can be maintained. Whilst soaring, generally the wings are held flattish or slightly flexed but sometimes with the hands lowered. About 90% of flight by these eagles in Israel was gliding or soaring. They often fly with the head dropped with hands arched in a glide or often arms straight out and hands drooped. The drooping wing flight method, peculiar to the steppe eagle as well as to the greater spotted eagle, is sometimes also called the “tuck”, and is thought to be a gust response precipitated by a transient drop in aerodynamic loading. Steppes adapt their flight to wind and thermal conditions as was studied in Israel, increasing their gliding airspeed under strong thermal convections or opposing winds. This study determined that a combination of circling in thermals and inter-thermal gliding was interspersed with soaring in straight-line glide. Israeli migrants flew up to 1600 m above the ground but 90% were under 1000 m and half were below 400 m. The Israeli steppe eagles were able to maintain a mean climbing rate of 1.9 m per second, a mean cross-country air speed of 12.4 m per second and a mean of 15.6 m per second in glides; the flight was similar as in other common raptors here but the steppe eagle attained the highest mean cross-country speeds. Steppe eagles tend not to be very vocal especially when not breeding. Their main call is a raspy bark which is similar to that a tawny eagle, despite being mildly deeper. In aerial displays, a loud whistle has been recorded, quite unlike any vocalization of a tawny eagle. Other call recorded have included mainly low and croaking notes aside from a high shriek when startled.
Steppe eagles appeared to have evolved the strategy of migrating from their breeding grounds, due in large part to the temporary seasonal availability of their main prey, ground squirrels. They probably migrate in greater numbers than any other eagle in the world and can appear to be frequent enough at migration sites that they may mask less numerous migrating eagles that are mistakenly missed in their ranks. The migratory behaviour of this species is arguably amongst the best studied aspect of its entire biology. Autumn migration often begins around October on fairly broad fronts, and may peak around late October. It usually ends in late November to December but steppe eagles frequently travel somewhat nomadically while not breeding and so individuals may not reach their winter terminus point until about January. Spring migration usually commences in February, peaking early from late February to March, with likely all gone from Africa by the end of the latter month, then continuing in a diminishing trickle into April and May. In passage at Suez, the steppe eagle is one of the earlier migrating raptors on average alongside the long-legged buzzard (Buteo rufinus), averaging about a month sooner in passage than the common buzzard (Buteo buteo) (the most common migrant there) and slightly sooner than the lesser spotted eagle, as well as much sooner than some other raptors there. On average, the wintering period in Africa is relatively brief, at a mean of about up to about 4 months (down to about 2), while adult steppe eagles spend up to 7 months (max of around 5 months for a young eagle) on their breeding grounds. In autumn records from Africa, younger eagles migrate the earliest and adults the latest. Radio-tagging studies confirmed, much as in the lesser spotted eagle, that in spring juveniles migrated later, wandering about more so and came back to the summering grounds much later. One young steppe eagle that was banded in passage in the United Arab Emirates wintered initially in Yemen before returning for the summer to Kazakhstan, then migrating to eastern Africa the following winter, showing that they can change their migratory habits over time. Many studies corroborate that steppe eagles generally migrate lesser distances as they age.
Peak movements around the Red Sea show as many as 76, 000 steppe eagles moving over Bab-el-Mandeb in the fall of 1987, with up to 65, 000 (in 1981) in Suez and up to 75, 000 in Eilat, Israel in the year 1985. Once migrating steppe eagles enter Africa in autumn, no mass migrations have been recorded anywhere for the species in the continent. Although not large, some semi-significant spring movements were detected in Egypt, despite none being recorded in the fall. In autumn, steppe eagles usually pass over Bab-el-Mandeb in the north of Red Sea while in spring they predominantly cross to the south of the Red Sea around Suez. The mean number of steppe eagles that annually pass over Eilat in spring are estimated at 28, 032 with a mean peak day of March 10th, making them roughly the fourth most common migrating raptor in spring there (and they often pass in intermingled flocks with other soaring raptors, but not those with powered flight). In Eilat, steppe eagles constitute 6.4% of all raptors seen, nearly all of the Aquila eagles seen and, among those that could be aged, an estimated 60-70% of the steppes seen were thought to be adults. More unusually, the steppe eagle may be the only raptor to also use Israel as a common migratory flight path in autumn as well as spring, with even commoner migrating raptors such as common buzzards and European honey buzzards (Pernis apivorus) being rare there in the fall. In Nepal over 2.5 weeks starting in October 20th, nearly 7852 steppe eagles were tallied, making up more than 80% of the recorded migrating raptors, with peak times of movement being between 10:00 AM and 4:00 PM, especially between noon and 2:00 PM. Over 3 years of study in Nepal, 21, 447 steppe eagles were recorded (as many as 1102 within a day and a mean of about 15.2 an hour) at the counting sites. Strong evidence of east-to-west migratory movements, rather than south or northbound, has been made in the Kathmandu Valley. It was indicated based on the directional studies that especially juveniles from the eastern part of the breeding may be more frequently migrate westbound to reach wintering areas such as the Middle East and Africa. On the contrary, juveniles and subadults during the wintering season seem to considerably outnumber adults in the Indian subcontinent so many do head due south. Of 3381 ageable steppe eagles in passage in Nepal, 56% were juveniles or immature, 44% were adults; of 7852 eagles, 58% migrated in groups of 1-5, 30% in 5-20 groups and 12% in larger flocks.In Himachal Pradesh of India, about 11, 000 steppe eagles were recorded in autumn migration in 2001 and about 40% less were counted the next spring. This study indicated different migratory paths being used in the seasons, presumably following the winds predominant direction around the terrain, with the westerly autumn migration mostly in the western Himalayas and the easterly spring migration more so in the east of Nepal. Staging areas are not well-delineated in India but appear to concentrate around feeding sites such as landfills. A single female that was radio-tagged in Mongolia was recorded to travel southwest and stop in southeastern Tibet, which is also the southernmost part of the species breeding range. The data from this female indicated that not all steppe eagles move to warmer climates and, based on that she remained stationary until her return to Mongolia, that she was not nomadic as many eagles of the species are. During return spring migration, the steppe eagles in passage in Nepal will reported amass into groups of approximately 5 to 20 eagles at only about 20 to 70 m above the terrain before rising up to cross between the snow-covered peaks.
16 radio-tagged eagles that returned in their first spring migration to their Kazakh summering grounds were recorded to winter as first-year juveniles either, in roughly equal measure, in the Arabian Peninsula or southern Africa, and covered straight-line distances, ranging from 3489 to 9738 km, although individually could meander up to 20644 km for one eagle migrating from wintering grounds Botswana. Of the 16 returning Kazakhstan eagles, spring migration lasted an average of 40 days, ranging individually from 38 to 54 days and covered a mean of 355 km each day. The migration path generally led the eagles around almost every direction of the Red Sea, many also passing over Israel and some wrapping around the Caspian Sea. A different radio-tagging study of 19 juveniles (about 57% of which survived) from Russian or Kazakh sites found that autumn movements in the 1st year migration averaged 4222 km and confirmed not only that they freely changed wintering sites anywhere from India to southern Africa but they never returned, surviving or not, to their natal site in the 1st year, instead return to wandering widely across the northern steppe. The 1st migration averaged 52 days and were much briefer for females than for males, with the discrepancies more pronounced for eagles originating from the Altai Mountains. 15 birds tracked in this study were found to have migrated most frequently to winter in south Pakistan (right along the borderlands to India) or in eastern Turkmenistan. Spring migration began on a mean date of March 25th for the 15 young eagles and lasted about 26 days on average, covering a mean of 3925 km, with females initiating migration on average 18 days later than males and migrating more briefly, more quickly and more often with fewer stops than males. 9 eagles which were tracked successfully in their first spring passage in this study wandering widely mostly in natural steppe hunting for squirrels and 8 of these tracked to their 2nd autumn migration took about 1.5 times shorter on their 2nd autumn passage and migrated about 17% less far on average.
The steppe eagle is an opportunistic predator like other Aquila eagles but has a number of dietary and foraging peculiarities. They prey mainly on small-sized mammals, with some birds and reptiles and (mostly in winter) frequently insects and carrion. Despite their opportunistic nature, the steppe eagle is a somewhat specialized predator on particular mammals such as ground squirrels while breeding and, during non-breeding times, feeds on various foods but is often peculiarly narrow in dietary selection, preferring massed food sources that require little effort for them to obtain. Various other small or medium-sized mammals can be become the most significant prey locally on the breeding grounds, such as voles, pikas and zokors and, generally more secondarily, marmots, hares, gerbils, hedgehogs and others. During the breeding season, one resource claimed that prey mostly weighs 50 to 250 g. Another account estimated that about 95% of prey weighed less than 250 g, although predominantly over 63 g. However, yet another resource claimed that staple prey for steppe eagles could weigh anywhere from 50 g up to 1500 g. Even the latter estimate may be conservative in size range, with prey species varying widely in size from very small insects from colonies to unexpectedly large mammals (and seldom birds) apparently killed near nests. On the other hand, a preference has indeed been detected for smaller burrowing mammals (i.e. probably under 250 g or so). Studies have determined where only larger species of burrowing mammals are predominant (even the larger species of ground squirrel), the steppe eagles appear to attain comparatively sparse nest densities, only occurring in high densities where the smaller burrowers are profuse. Ecological partitioning to limit interspecific competition may be a factor that dictates the steppe eagle’s preference for relatively small prey. The breeding steppe eagle mainly hunts in a low soaring or gliding flight, at a maximum of 200 m, diving or making short, accelerated stoops onto their prey. Usually, they tend to capture their prey on the ground. Steppe eagles have been recorded in both Kazakhstan and Mongolia to tactfully avoid casting a shadow before descending onto prey and may drop stones to provide a distraction, a probable form of tool use. In the Kazakh observation, the steppe eagles quickly became used to agricultural activity adjacent to prey accesses while they hunted. They also may hunt in any season on the ground, moving with a shambling gait as necessary, and may give chase on foot to both vertebrate and insect prey. Steppe eagles can often ambush prey by standing in wait next to burrows, suddenly pouncing quickly onto the quarry upon its emergence. Steppe eagles have been seen in China to buzz through locust swarms on the wing as well as to taking avian prey from over 200 m above the ground in a dive. Tandem hunting by pairs has been recorded during the breeding season while, in winter and migration, these may be the most social of all eagles, often sharing by up to the dozens abundant food sources. The non-breeding steppe eagle flocks may even seem to assist one another in procuring prey from which they themselves are not likely to be able to directly profit and may repeatedly assist each other until all flock members are satiated. If confirmed, this mutually beneficial foraging strategy between presumably unrelated eagles is truly unique. Much like the tawny eagle, the steppe eagle will readily rob other raptors of their catches, approaching from any angle and pursuing closely until the victim is forced to land or drop its food.
The single prey species most strongly associated with the steppe eagle is the little ground squirrel (Spermophilus pygmaeus). In some areas, as much as 98% of the diet reportedly can be little ground squirrels. This is a smallish ground squirrel though is actually not greatly smaller than many other Eurasian ground squirrels, at a mean adult weight of about 235.2 g. The little ground squirrel once reached densities of around 30-40 per hectare and provided a reliable food source for these eagles. However, this species has plummeted in population density, in Kalmykia for instance going down from abundant in diverse habitats to perhaps locally extinct before gradually trickling back up in numbers (which continue to be a mere shadow of what they once were). The local steppe eagles of Kalmykia continue to show a strong preference for little ground squirrels. A continued primary reliance on little ground squirrels by steppe eagles was also found recent in studies from Saratov and Lake Baskunchak as well. Out of Russian, in the Karaganda Region of Kazakhstan, little ground squirrels again were an important identified food source, at 19.25% of 400 prey items. In the general area between the Aral Sea and the Caspian Sea, 112 prey items were led by little ground squirrels, at just over 33%. However, in this data, the little ground squirrels were closely followed in number (29.7%) by the yellow ground squirrel (Spermophilus fulvus), which, with seasonal weights ranging from 500 to 2000 g, is the largest of Eurasian ground squirrels. The little ground squirrel is only found in a substantial portion of the western part of the range, so elsewhere steppe eagles tend to prey on different prey species while breeding, though generally continue to take small burrowing mammals, of course.
Around Lake Balkhash in Kazakhstan, the main prey was reportedly the red-cheeked ground squirrel (Spermophilus erythrogenys), a slightly larger ground squirrel than the little species at a mean adult weight of 355 g. Other prey noted here included Pallas's pika (Ochotona pallasi), Libyan jird (Meriones libycus) and tolai hare (Lepus tolai). In Xinjiang, reportedly the main prey species is the long-tailed ground squirrel (Urocitellus undulatus). In the Altai region, the leading prey may be the Siberian zokor (Myospalax myospalax), which is the size of a large ground squirrel at an adult weight of about 453 g. However, some report in the Altai region that the main prey is the long-tailed ground squirrel and the migration arrival times do seem to correspond closely with this species hibernation emergence period. Another potential primary prey resource is reportedly the gray marmot (Marmota baibacina). All the primary prey in the previously little reported Altai population are as adults well over what is considered the typical prey size range for this eagle, such as long-tailed ground squirrels, zokors and marmots as well as ptarmigan, and in turn this may favor the large size of the steppe eagles from this region. On the contrary, other predominant prey in steppe eagle nests can be even smaller than ground squirrels. In Mongolia, the main prey by a large margin was reportedly the Brandt's vole (Lasiopodomys brandtii), which weigh about 40 g. In the Transbaikal region, the main prey may be the Daurian pika (Ochotona dauurica), which weighs about 155 g. This pika can account for around 39%, as was the case in 62 prey items, (and perhaps up to 62% locally) of the diet in the region. Another study reported a very different primary food source for the Transbaikal, which was the young of the much larger Tarbagan marmot (Marmota sibirica), which were estimated in the study to be from 55 to 77% of the annual diet. Even more conflicting data found that some Transbaikal steppe eagles derived as much as 70% of their foods from long-tailed and Daurian ground squirrels (Spermophilus dauricus). It is possible that in both Altai and Transbaikal that the shifts to differing reported primary prey species are responses of the eagles to shifting prey availabilities as many burrowing mammals are subject to population cycles as well as human-sourced depletions. While rodents and some lagomorphs are usually favored in the diet, in some areas steppe eagles can live at least in part off of quite different prey such as long-eared hedgehogs (Hemiechinus auritus). Other notable prey taken regularly whilst breeding by steppe eagles includes steppe pika (Ochotona pusilla) (especially in the Volga region), alpine pika (Ochotona alpina), yellow steppe lemming (Eolagurus luteus) (especially in eastern Kazakhstan), or the slightly larger types of gerbil such as great gerbils (Rhombomys opimus) and Mongolian gerbils (Meriones unguiculatus). The study of the Karaganda region of Kazakhstan with 400 prey items found illustrated that the steppe eagle is capable of deriving a living from a wide range of prey, with the foods led by rosy starling (Pastor roseus) (mostly fledglings), at 24%, unidentified Microtus voles, at 19.75%, followed by little ground squirrels, unspecified pikas (8.25%), European hares (Lepus europaeus) (5%) and grey partridges (Perdix perdix) (4.5%). An aptitude for avian prey was detected in Transbaikal particularly, including Daurian partridge (Perdix dauurica) and Japanese quail (Coturnix japonica) (the latter at up to 15.6% of the diet). In Altai, assorted corvids (at up to 24.2% of the diet), probably mostly rooks (Corvus frugilegus) and Eurasian magpie (Pica pica), were important to diet as were willow ptarmigan (Lagopus lagopus). Within the Saratov area, medium-sized birds were frequently reported in the diet, such as grey partridges, little bustards (Tetrax tetrax), northern lapwings (Vanellus vanellus) and rooks. A diversity of small passerines has been found in the diet, especially fledgling-age larks of various species, most frequently perhaps in Kazakhstan and Mongolia. A few reptiles found in the diet around nest have included at least sand lizard (Lacerta agilis), Caspian whipsnake (Dolichophis caspius) and steppe viper (Vipera ursinii).
On occasion, during summer, a steppe eagle may be able to take exceptionally large prey. The most regular large prey to appear in their diets are usually Tolai hare, at about 2 kg, and assorted marmots. The upper size of marmots that the steppe eagle may attack is not well-established although some of the species regularly hunted by these eagles have extremely large average adult weights, i.e. around 8 kg, but the typical size taken by this eagle is more likely around 1.5 kg (i.e. for small emergent juvenile marmots). The steppe eagle takes a diversity of mammalian carnivores including mountain weasel (Mustela atlaica), marbled polecat (Vormela peregusna), steppe polecat (Mustela eversmanii), kits of Eurasian badger (Meles meles) and possibly live adults (i.e. “fresh remains”) of 2.7 kg corsac fox (Vulpes corsac) and 6 kg red fox (Vulpes vulpes). A surprisingly range of young ungulates have also been found in small numbers and it is likely that some are taken both as carrion and as kills, including goitered gazelle (Gazella subgutturosa), Mongolian gazelle (Procapra gutturosa), saiga antelope (Saiga tatarica) and domestic goat (Capra aegagrus hircus). In newborns of these species, weights can vary from around 2 kg (in goats) to about 3.5 kg (in saiga antelope). The taking of large birds is less well-documented than predation on large mammals and in some cases both in summer and during non-breeding times certainly pertain to nestling predations, such as on storks and cranes, or to pilfering easy large fowl like chickens (Gallus gallus domesticus) or domestic turkeys (Meleagris gallopavo).
The steppe eagle, despite being one of the most numerous and widely distributed of all eagles, is exceptionally poorly studied in its non-breeding dietary habits. This is due in large part to the nomadic behaviour displayed by most (but not all) steppe eagles during these times. Steppe eagles are fairly different from related species, being rather gregarious and non-predatory while away from their breeding grounds. Exceptionally, some steppe eagles have been known to overwinter in Altai Town, Kazakhstan, living reportedly off of brown rats (Rattus norvegicus) and rock doves (Columba livia). They are often seen congregating at feeding sites with easily obtained foods that are available in large quantities. In southern Africa, these eagles are often associated with rain fronts and the humidity that accompanies them. They do this largely to exploit a certain food source, termite alates. Termites are known to emerge more extensively in these conditions and so the steppe eagle, not unlike other long-distance migrant raptors, can become locally rather insectivorous to the exception of virtually any other foods. Most often, these eagles will fly down when it is noticed that termites are emerging or wait on foot and then grab them. According to one account these large eagles feed on termites "lumbering after their minuscule quarry in ludicrous fashion". They have also sometimes been seen to take termites in the air and feed on them in flight, not any easy task for such a large eagle. Roosts near termite colonies can contain several steppe eagles which may remain over days but generally depart whether well-fed or not if the rains disperse. In Namibia, the roosts used were the tops of quite small trees of only 2 to 3 m height. Although tiny with an average estimated weight of only 0.15 g, the harvester termite (Hodotermes mossambicus) (the main termite prey) have been deemed highly nutritious with a relatively high caloric value. It has been estimated that a steppe eagle would have to eat approximately 1600-2200 termites a day, which can be attainable in about 3 hours of feeding. The stomachs of 2 dissected steppe eagles contained 630 and 930 termite heads, respectively. In Zimbabwe, steppe eagles have also been seen in feeding masses in stubble fields picking out insects. However, it would reductive to consider the steppe eagle largely insectivorous in winter, since disproportionately the eagles seen feeding on termites in southern Africa were juveniles and immatures and many of the species winter outside of southern Africa; often wintering steppe eagles from other areas do not seem to live predominantly on insects. In east Africa, the diet of steppe eagles is poorly documented but is reported to consist largely of silvery mole-rats (Heliophobius argenteocinereus) and blesmols of the genus Cryptomys. Routine predation, probably on young or weak individuals, by steppe eagles has been recorded amongst flamingo colonies in east Africa. In several parts of Africa, steppe eagles may routinely visit and feed off of the colonies of the super-abundant bird, the red-billed quelea (Quelea quelea), with a noted focus on picking off the seemingly innumerous nestlings and fledglings of this small passerine. The steppe eagles will reportedly do so by ungracefully scrambling amongst the branches of the nesting colonies.
In the Indian subcontinent, the steppe eagle appears to fulfill the role of a weakly predatory opportunist. Individual Indian wintering steppe eagles are reported to feed at times of vulnerability of prey, including injured birds, eggs and young water birds from heronries, while groups of the eagles often occur around carrion, masses of stranded fish, poultry farms, garbage dumps and livestock carcass dumps. In Chari-Dhand wetlands, as many as 1000 steppe eagles have been seen to gather, presumably living largely off of vulnerable water birds. At the city dumps of Pune as many as 200 steppe eagles have been known to gather and feed. A carcass dump in Jorbeer near Bikaner was recorded to host an average of 43 steppe eagles per day during winter, with a peak number generally occurring in January and February (common dates from November to March and more rarely from September to May), with as many as 136 steppe eagles plus at least 9 other large raptors (mostly vultures), many of which are considered threatened species. It was found the Jorbeer carcass dumps enticed the steppe eagles to venture away from the normal wetland or wetland-adjacent areas used by steppe eagles in the area to the desert-like region, but feral dogs could, in some years, appear to chase off and cause the eagles to avoid this dump. A concentration of around 50 steppe eagle was seen to feed on swarms of locusts in Nepal. Perhaps to avoid competition (i.e. from vultures, jackals and so on) and to monopolize a food item, steppe eagles in India appear to come largely to smaller carcasses such as those of jungle cats (Felis chaus) and pythons. In the Banni Grasslands Reserve, steppe eagles are reported to largely hunt for food unlike in many other Indian reports, mainly on lesser bandicoot rats (Bandicota bengalensis), although also sometimes stole prey from other raptors. Similarly, active predation was unusually reported in Saurashtra and on larger prey including mongoose and Indian hare (Lepus nigricollis) as well as an unsuccessful attack on a mountain gazelle (Gazella gazella) fawn.
In the region of Bharatpur, Rajasthan, largely around Keoladeo National Park, the foraging activities of steppe eagles have been observed extensively. The steppe eagles seldom actively hunted, instead alternating between capturing nestlings from the heronries, especially nearly fledgling-age young of late nesting painted storks (Mycteria leucocephala), and engaging in kleptoparasitism towards other birds of prey, often doing so in groups of about three to nine eagles. More infrequently, steppe eagles in Bharatpur have been seen hunting flocking birds, fish (usually stranded), lizards and snakes. The steppes have been observed feeding on freshly killed young water birds at Bharatpur at daybreak and during early mornings and so may hunt while taking advantage of bright moonlight. Piracy against other raptors often resulted in food wastage, since the steppe eagles often forced the other raptors to drop their catch but the steppes were unable to intercept them and the kills were frequently lost into the water. In Bharatpur, the steppe eagles tended to perch relatively low compared to other eagles, at about 9 to 10 m in the trees, and to perch often for longer periods than other raptors, apparently while watching closely the activity of the other birds of prey. Of a total of 49 observed hours of activity for steppe eagles in Bharatpur, 45% of it was spent foraging, with a maximum foraging time of 69% during January, then reduced in March to only 17%. The daily food intake of individual steppe eagles was extremely low relative to their size, at only 141 g. Instead of piracy, the steppe eagles often engaged each other in what can be considered a play display, almost exclusively between juvenile steppe eagles. In it, two birds circled 100 m or more, the higher bird circling closer and dropping toward the lower bird with extended feet, forcing it to roll over and present talons, they either immediately disengage with or without locking talons or descend looked for a few metres before separating; often steppes will fly purposely at a conspecific that is circling and fly up to a higher position so it can drop onto the other; in another incident, a steppe grabbed a plastic bag and let it go buffeting by the wind, then repeatedly caught it and let it go again, ultimately being joined by 5-6 other steppes in the "game'.
Less study has been conducted on feeding habits of the wintering and migrating steppe eagles in the Asia Minor, Middle East and Arabian Peninsula. What is known suggests that they, even more strongly than wintering steppe eagles in Indian subcontinent, today frequent various waste food sources inadvertently provided to them by humans. In Muscat, Oman, migrants largely from Kazakhstan were recorded to live off a mixture of refuse from the region’s main landfill and large-scale carcass dump sites. As in the carcass dump areas of the Indian subcontinent, these carcass dumps often host a wide array of large birds of prey, both migrating species and non-migratory ones. In keeping with its size, steppe eagles dominated slightly smaller eagles and vultures and were in turn dominated by slightly larger eagles and much larger vultures. High use of slaughterhouses and cattle dump sites was recorded in winter in Iran. Interestingly, the Iranian slaughterhouses and dump sites hosted no first-year juveniles and few adults, but many steppe eagles either aged to 2 to 3 years of age (62.5%) or 4 to 5 years of age (33.3%). Foraging in both dump sites and available wetlands has been recorded in Iraq as well. Incidental feeding observations from Armenia suggests that steppe eagles in passage and in winter there are able to capture large quantities of voles or pirate them or similar small prey from smaller species of birds of prey.
Interspecific predatory relationships
The steppe eagle shares its distribution with several other birds of prey that can compete for resources. Most similar in feeding niche are largely other eagles, many of which are also similarly migratory. One eagle of similar central distribution is the eastern imperial eagles. The imperial eagle has a similar morphology and can broadly overlap in food selection. It also takes many ground squirrels but is generally less specialized on them during breeding, and often takes similar or larger numbers of prey such as hares, hedgehogs, hamsters and assorted birds both large and medium. In general, the dietary biology is better understood, prey is taken of more diverse sizes and the prey spectrum is far more diverse (perhaps nearly three times as many recorded prey species) in the imperial species. The average weight taken of prey like young marmots is similar in both eagles, averaging 1.5 kg in the eastern imperial while the steppe also takes marmots of around this size. Although not common, the imperial eagle can sometimes take prey weighing over 2 kg, probably rather more frequently than the steppe eagle. It is possible that the steppe eagle gained the preference for relatively more numerous and social but quite small mammals as prey to avoid heavier competition over slightly larger but often more dispersed terrestrial mammals (i.e. hares, hedgehogs, etc.), especially those taken by imperial eagles. Also, the imperial eagle is rather more predatory in food obtainment while wintering, not infrequently eschewing the more vulnerable nestling water birds in the Indian subcontinent to take many adult birds such as waterfowl and coots. The eastern imperial eagle differs most significantly from steppe eagles in nesting habits, favoring tall trees, sometimes in fairly well-wooded areas, which quite contrary to the steppe eagles ground nesting preferences. The migratory course used by imperial eagles is largely the same as the steppe eagle but the imperial is the far less numerous migrant (also more frequently overwintering near their breeding ground) and radiates less far in winter (especially in Africa). Despite the steppe eagle averaging scarcely smaller, data from both breeding and wintering areas indicates that the imperial eagle tends to be behaviorally dominant over steppe eagles. This has manifested in full or partial displacement of steppe eagles locally using pylons as nesting sites by imperial eagles. Furthermore, at shared feeding sites, the steppe eagle tends to back down to the imperial eagle, often allowing it to feed first despite occasional displacement of imperials with full crops. On occasion, in India, steppe eagles succeed in pirating prey from imperial eagles, normally in cooperating parties of steppe eagles. In at least one case in India, the steppe eagle was the aggressor in an interaction with an eastern imperial eagle, causing the two eagles to lock talons and cartwheel down with uncertain results. While the eagles are expected to correspond their sizes in hierarchy when nests are located in the same general area, wit
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- Aquila nipalensis
- Thai: นกอินทรีทุ่งหญ้าสเต็ป, nok in-sree thung yaa sa-tep
- Aquila rapax nipalensis
Least Concern (IUCN3.1)