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Imperial Eagle Aquila heliaca Scientific name definitions

Bernd-Ulrich Meyburg and Guy M. Kirwan
Version: 1.0 — Published March 4, 2020
Text last updated July 31, 2013

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Field Identification

72–84 cm; male 2450–2720 g, female 3160–4530 g (1); wingspan c. 180–215 cm. Generally dark brown ; crown, nape , sides of head and neck have pale tawny-buff lanceolate feathers producing a pale patch. White shoulder patch, or epaulette, much smaller than in A. adalberti. Female larger up to 10% larger (e.g. wing 565–661 mm, versus 540–622 mm in male) and 40% heavier (1). Immature starts pale brown with variable dark streaking, and blackish flight feathers, with distinct white trailing edge to wing, regularly streaked breast, and head and rear body very pale and plain (2); passes through darker, very patchy plumages over several years, before attaining adult plumage after six years and via six distinct different plumages (2). Principal confusion risks are with A. rapax, Clanga clanga (especially so-called ‘fulvescens’) (3), older immature A. nipalensis and A. chrysaetos (1). Juvenile might also be confused with A. verreauxii, principally in the Afrotropics (4).

Systematics History

Formerly considered conspecific with A. adalberti. E populations have occasionally been separated as race ricketti, but generally considered undiagnosable. Monotypic.

Subspecies

Monotypic.

Distribution

C & SE Europe (from Austria, E Czech Republic, Slovakia and N Hungary) and Turkey, Georgia, Armenia and Azerbaijan E to NW China (W Xinjiang), C Transbaikalia, probably N Mongolia and perhaps NE China (Inner Mongolia), in breeding season reaching N to c. 55° N in European Russia. Winters S to NE & E Africa (S to Kenya, exceptionally N Tanzania; once to Cameroon), Arabia, Iran, E Afghanistan and N Indian Subcontinent (from E Pakistan to Bangladesh, S to Gujarat, more exceptionally Maharashtra and even Tamil Nadu), E & SE China, N Myanmar (once), Thailand, N Indochina and recently S to Singapore; occasional in winter N to Primorye (SE Russia), Korea and Japan (mainly Honshu, but also Shikoku, Kyushu and Ishigaki-jima), as well as Taiwan.

Habitat

Originally bred on old isolated trees in plains of C & SE Europe, but has subsequently retreated to large forests in mountains, as result of persecution and habitat alteration. In Slovakia and Hungary, where now well protected, starting to reoccupy former habitats. Hunts in open, often cultivated, areas. Recorded to 2000 m in Turkey (5).

Movement

Mostly migratory. Birds migrate to S Turkey, Iran, Israel , Iraq, Egypt and Arabia, and to Pakistan, India, Laos and Vietnam, more recently (since mid 1980s) (6) moving as far S as Singapore and elsewhere in Peninsular Malaysia (1). However, main wintering grounds are probably in Middle East. Leaves breeding areas mid Sept to mid Oct/Nov, returning in Feb–Apr/May (1), with passage through Israel in autumn recorded between 9 Sept and late Nov (most between 5 Oct and 10 Nov), and in spring between mid Feb and 25 May, with most during late Feb to mid Apr (7). Numbers passing migration watchpoints are usually small; in Middle East, largest numbers in autumn, exceptionally 556 at Suez, Egypt, in 1981, and 178 in 1984 (8), and 309 at Ghadir Burqu, Jordan, between 24 Sept and 20 Oct 1998 (9), whereas in spring maximum of just 95 at Eilat, Israel, in 1977, and only small numbers through Turkey at either season (7) (recorded 30 Mar–24 May at Bosphorus) (10); in China, ten at Beidahe in 1986, between 15 Sept and 28 Oct, was highest total in period 1986–1990 (11); on SW shore of L Baikal, moves S between 4th and 15th Oct, but much further S, in Nepal, passage of all age classes observed between late Oct and early Nov (12). In spring, reaches Russian and Chinese breeding grounds in late Mar or early Apr (12). On passage through Israel generally accompanies larger numbers of A. nipalensis (through Eilat) or Clanga pomarina (through northern valleys) (13). Arrives on wintering grounds in SE Asia in early Nov and remains until at least mid Mar (6); in Kenya also Nov–Mar (14), but extreme dates in Ethiopia 2 Oct–24 Mar (15). Satellite-tracking has revealed at least some winter site faithfulness across years; of eight birds trapped in Saudi Arabia in winter, four migrated to Russia in spring, one to Kazakhstan and one to NW China, with distances between summer and wintering areas ranging between 3900 km and 5000 km (16). Others breeding in Kazakhstan have also been sighted in Arabia, from Kuwait in N, S to Oman and Yemen (17). However, further E, young from L Baikal region were satellite-tracked through E Mongolia and C Inner Mongolia (China) to their wintering grounds from S China to Thailand; siblings independently used same migration flyway, but flyways differed between families (18); one juvenile wandered widely during winter period, between Yunnan (SW China), E Myanmar and N Thailand (12). In Slovakia and Hungary, adults often seem to remain at or near breeding areas, and same may be true in parts of Turkey (1) and on Cyprus (19), while in Arabia young birds predominate in Oman, whereas in further N in Jordan (20) and Saudi Arabia (21), adults appear equally numerous, and in Central Asia, species is recorded as far N as Kazakhstan at this season (22). Vagrants recorded in various Western Palearctic countries including Poland, Finland (three records, first in 1981) (23), Sweden (at least eight records) (23), Norway (first seen Feb 2007) (24), Denmark (at least 18 records) (23), Germany (most recently in 1991) (23), Netherlands (Apr 2005) (25), France (three records, all in 19th century) (23), Italy (c. 10 records prior to 1990s) (23), Malta and Libya (1). In sub-Saharan Africa reported W to Cameroon (Nov 1993) (26), Nigeria (Nov 2001) (27) and SW Niger (Nov 2012), the latter a juvenile satellite-tracked from its breeding area in Hungary (28).

Diet and Foraging

Small to medium-sized mammals; in most areas main prey species are susliks (Citellus, Spermophilus) (29) and hamster (Cricetus cricetus). Birds (including domestic chickens) (29) generally taken in small proportions: 22% in Hungary, compared to 65% C. cricetus; nowadays main prey in Ukraine. In N Aral region, feeds mainly on rodents, especially (70–74%) great gerbils (Rhombomybs opimus), but also susliks (7–25%), reptiles (19–23%) and birds (7–15%), with insects, tortoises (Testudo), amphibians and crustacea (12) also taken, at least in some areas (29); for example, reptiles such as spiny-tailed lizards (Uromastix hardwickii), monitor lizards (Varanus spp.) and at least once a Russell’s viper (Vipera russelli) are probably more preferred in arid habitats (12). In S Urals, 27 species of vertebrates recorded, ranging in size from mice and voles to hares and foxes (1), with more birds than mammals. In NC Kazakhstan > 150 prey species have been recorded, of which the most important are mammals, primarily marmots (Marmota bobac), susliks (Spermophilus fulvus, S. major, S. pygmeus), steppe pika (Ochotona pusilla) (30), hares (Lepus spp.), foxes (Vulpes vulpes and V. corsac) (30) and small mammals (Muridae), and birds including corvids (Corvus corone, C. frugilegus), Little Bustard (Tetrax tetrax), owls (Asio flammeus and A. otus) (30), waterfowl and raptors (31); this multi-year study found that overall diet did not change from year to year, but significant among-year differences were found in use of six types of prey: harriers (Circus), mice and voles, owls, Black-billed Magpie (Pica pica), yellow suslik (Spermophilus fulvus), and foxes (30). Around L Baikal, prey recorded at nests included long-tailed susliks (Spermophilus undulatus), Carrion Crows (Corvus corone), a vole (Microtus sp.), a duck (Anas sp.), steppe polecat (Mustela eversmanii) and domestic ducks and chickens (32), with the suslik comprising c. 47–72% of prey and mouse-like rodents (e.g. Microtus gregalis, M. oeconomus, Arvicola terrestris) another c. 3–7% (12). Takes raptors up to size of Western Marsh-harrier (Circus aeruginosus) (1) and Hen Harrier (C. cyaneus) (12), with birds probably increasingly important in better-forested habitats (12). Other avian prey recorded includes a grebe (Podiceps sp.), Bar-headed Goose (Anser indicus), Ruddy Shelduck (Tadorna ferruginea), Spot-billed Duck (Anas poecilorhyncha), young Greater Flamingo (Phoenicopterus roseus), Common Kestrel (Falco tinnunculus), Daurian Partridge (Perdix dauurica), a francolin (Francolinus sp.), Northern Lapwing (Vanellus vanellus), Common Sandpiper (Actitis hypoleucos), Rock Dove (Columba livia) and crows (Corvus spp.), some of which may have been pirated, as well as eggs and chicks of colonial waterbirds (12). Reports of predation on crabs, fish and other intertidal items remain unconfirmed (12). Carrion also eaten, especially in winter and during migration, when visits refuse tips, landfills (33) and slaughterhouses (34), for example in the Middle East (35); also pirates food from other raptors as large as A. rapax (12), and this may an important feeding method in Indian Subcontinent in winter (1). In winter quarters, in Jordan, diet includes 14 identified species of mammals, birds and reptiles, with large domestic animals (sheep and goats, probably consumed as carrion) predominating (53·7% of analyzed items), followed by presumably live-caught birds (26%, nine different species) and small and medium-sized mammals (19·7%, e.g. Felis sp., Paraechinus aethiopicus, Lepus capensis, Meriones crassus, Jaculus jaculus) and reptiles (0·6%) respectively (20). Prey caught mainly on ground by perch hunting or by soaring, usually with a short stoop or dive to ground, and pair members often hunt co-operatively (1). Non-territorial birds often associate with other large eagles such as Haliaeetus albicilla and Clanga clanga at wintering sites.

Sounds and Vocal Behavior

Mostly vocalizes during breeding season, the main call, principally given during aerial displays, being a deep, harsh, barking “owk owk...” or “kraw-kraw...”, which is repeated rapidly 8–10 times, or 13+ times in display, and is deeper and harsher than similar call of A. chrysaetos, or sometimes more croaking; also given from perch and by female when male arrives at nest with prey (1). Gives soft “ko-wok, wk wk wk” in alarm at distant intruder, as well as a harsher “gek” (1). Captive bird produced rising and falling trill, perhaps in alarm, although precise function unclear (1).

Breeding

In Hungary, adults appear in breeding areas in late Feb or early Mar, depending on weather conditions; laying completed by late Mar or early Apr, but in NW China season only starts in Apr (12); season in Pakistan, where no longer breeds, said to have been Nov–Apr (1); in SE Siberia adults laying late Apr to early May (12), incubating in mid May, with young probably fledging in mid Aug (32). Solitary. Large stick nest , constructed by both pair members (36), usually 100–150 cm in diameter and 60–70 cm deep (exceptionally 240 cm × 180 cm) (1); nest cup lined with green sticks, but also other materials, e.g. grass, fur, wool; almost always nests on trees , typically 4·5–25 m above ground (12), e.g. on Aleppo pine (Pinus halepensis) on Cyprus (19), Calabrian pines (P. brutia) and Quercus oaks in Greece (29) and in Pinus, Betula and Populus in Kazakhstan (37), very rarely on ground or cliffs in Turkey (5) and Kazakhstan, and occasionally on low shrubs, just 2 m above ground (1). In areas of Kazakhstan shared with other eagles, e.g. A. chrysaetos, A. nipalensis and Haliaeetus albicilla, the present species generally nested further from the other species and at mean distances of c. 1·5 km from conspecifics, even in areas with well-preserved habitat and relatively high densities (37), although population density was correlated with the degree of diet specialization (pairs with specialized diets nested closer to their neighbours) (31), but around L Baikal mean distance from centre of nest cluster in one territory to that in nearest territory was 17 ± 6·6 km (range 4–26 km) and pairs appeared to use areas of c. 12–15 km2 for hunting around nest sites (32). Pairs usually have 2–3 nests within a given territory, being used in different years (5); nests subject to frequent reuse over many years can become extremely large and other bird species may ‘co-habit’, e.g. pair of Common Kestrels (Falco tinnunculus) and multiple pairs of House (Passer domesticus) and Spanish Sparrows (P. hispaniolensis) at nest in Turkey (5). Clutch 2–3 eggs (1–4), dull white or pale buffish, with small brown, purple or grey markings, mean size 73 mm × 57 mm, laid at two - or -three-day intervals (36); incubation 43–45 days, mainly by female, provisioned by male, starting with first egg (36); chicks have white down , with cere and bill edges yellow, rest of bill black and has blackish-grey eye-patch (36); fledging 65–77 days, but young may remain with adults throughout winter (36). However, fledglings usually disperse more rapidly than those of A. adalberti, leaving the natal area after c. 4 weeks (38). Although 2–3 eggs may hatch, at least in Europe usually only chick survives (5). In Kazakhstan, pre-adults and non-breeders may gather into large and dynamic roosts, sometimes numbering almost 300 birds (39). Sexual maturity before adult plumage acquired at 5–6 years; pairs with both partners in subadult plumage have successfully reared young. Longevity 21 years in captivity; record of 56 years in captivity not confirmed; another case of a bird, first held in captivity for several years, later free living for 55 years, but equally unconfirmed. Breeding success: in Slovakia, 1·6 young per successful brood, or 0·76 young per pair per year (similiarly 0·7 in Kazakhstan) (40); in Hungary 1·5 young per successful brood, but 36% of breeding attempts unsuccessful. Adult survivorship in NC Kazakhstan is 84%, an unusually low figure among raptors and perhaps indicative of legacy of habitat degradation, human over-exploitation, or low nesting site fidelity (40).

VULNERABLE. CITES I. Legally protected in Armenia, Azerbaijan, Bulgaria, Croatia, Georgia, Greece, Hungary, Romania, Slovakia, Turkey and Ukraine. Overall, population most recently estimated by BirdLife International at 2500–9999 mature individuals within huge range of 8,250,000 km2. Rapid decline in Europe (and probably Asia) since World War II; formerly very common in many areas, e.g. 19 occupied eyries in 1000 km2 near Sofia (Bulgaria). Until recently, only in Slovakia and Hungary was species well protected and increasing, aided in part by provision of artificial nest-sites (23), although species started to recolonize Austria in 1989 (where lost as a breeder after 1810) (23) and even more recently the Czech Republic (41) (the latter the result of targeted conservation efforts) (42). As recently as early 1990s, European population thought to be just c. 350 pairs as follows: 30–35 in Slovakia; 35–40 in Hungary ; ten in Serbia; four in Macedonia; 0–2 in Greece (where finally lost as a breeder in 1993) (29); 15–20 in Bulgaria; probably few in Romania; 10–12 in Moldavia; 130–150 in European Russia; 35–40 in Ukraine; 50–150 pairs in Turkey, where formerly much more widespread (5); 9–11 in Georgia; 40–50 in Azerbaijan; c. 10 in Armenia. Just 1–2 pairs perhaps persist on Cyprus (19). However, in 2011, European population thought to number 1800–2200 pairs, considerably higher than estimates of 1051–1619 pairs, in 2000, and 1110–1624 pairs, in 2008, partly due to increased survey effort. For example, in late 1990s there were > 200 pairs between E Ukraine and middle Volga R, up to 250 pairs between the lower Don and lower Volga, with much smaller numbers in the Crimea (5–7 pairs) and N Caucasus (20–30 pairs) (43). Nevertheless, traditional survey methods may underestimate numbers, even of such a large and theoretically more easily detected species; at a study area in Kazakhstan, in 2004, comprehensive genetic and observational analyses determined that 414 eagles (308 non-breeders, 68 territory holders and 38 chicks) were present, which estimate was 326% larger than the 127 birds visually observed (21 non-breeders, 68 territory holders and 38 chicks) and 265% larger than the population predicted by demographic models with the same number of breeders (44). Populations in Volga region currently stable, but suspected to decline in future due to threats at breeding sites. Balkan population of 76132 pairs is now concentrated in Bulgaria and Macedonia, and is apparently stable, while recent surveys in Azerbaijan found relatively high densities on NW plains, estimating 5060 pairs within a 6000 km2 study area, and a total population size of 50–150 pairs. Perhaps formerly bred in Lebanon (45). Larger numbers in Asia, although lost as breeder in Afghanistan, Pakistan (1) and India (one old record from Haryana) (12), with population in Kazakhstan estimated at 750–800 pairs in late 1990s (of which 25–34 nesting pairs in Naurzum Zapovednik) (37), but more recently perhaps 35004000 pairs; estimated total for Asian part of former USSR as low as 800–1200 pairs. Of these, the Baikal population showed a steep and perhaps accelerating decline in numbers, between 1950 to 2005 in the Irkutsk region (W of Baikal) from 300 to 25–30 pairs (46), while in 1999 Baikal population was c. 70–90 pairs (compared to 250–300 pairs in 1950s and 150–200 pairs in early 1980s) (32), with 270–390 pairs in Siberia as a whole (18). Still breeds relatively widely in L Baikal region, dramatic decline in numbers is thought to be largely due to ploughing of steppes thereby reducing availability of Daurian suslik (Citellus dauricus), the species’ main prey in this region, and due to removal of large trees required for nesting (47). Other problems throughout range include: shooting, especially of young birds, in many areas, most intensively in Syria and Kuwait (48); trapping for trade (Jordan (20), Kuwait) (49); poisoning, intended for wolves and foxes; removal of young from nest, for zoos and other raptor keepers; habitat alteration, especially agricultural intensification (a significant factor in countries such as Kazakhstan (50), but also on wintering grounds) (51); mortality through electrocution or injury caused by collisions with power lines (mitigation efforts are underway in some areas, e.g. Slovakia) (52). International working group for species has been formed, and three meetings held in Hungary. Conservation Action Plan for European population published in 1996 and implementation reviewed in 2010, while Regional Action Plans have been published for Balkans and for Southern Caucasus; management guidelines for Hungary published in 2005 and are under preparation for Slovakia.

Distribution of the Imperial Eagle - Range Map
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  • Year-round
  • Migration
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Distribution of the Imperial Eagle

Recommended Citation

Meyburg, B.-U. and G. M. Kirwan (2020). Imperial Eagle (Aquila heliaca), version 1.0. In Birds of the World (J. del Hoyo, A. Elliott, J. Sargatal, D. A. Christie, and E. de Juana, Editors). Cornell Lab of Ornithology, Ithaca, NY, USA. https://doi.org/10.2173/bow.impeag1.01
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