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Pallas's Fish-Eagle Haliaeetus leucoryphus Scientific name definitions

Jaume Orta, David Christie, Guy M. Kirwan, and Christopher J. Sharpe
Version: 1.0 — Published March 4, 2020
Text last updated January 9, 2018

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Field Identification

72–84 cm; male 2000–3300 g, female 2100–3700 g (1); wingspan 180–215 cm (1). Mainly brown plumage , with head and neck golden sandy buff ; rounded tail dark brown with conspicuous broad white band . Female somewhat larger than male (e.g. wing 558–624 mm, versus 545–585 mm in male) by up to 19% and averages 9% heavier (1). Bare parts: irides dark brown to dark grey, cere pale blue-grey occasionally yellowish, bill dark greyish blue with darker tip; legs whitish to dirty yellow (1). Main likelihood of confusion is with H. ichthyaetus, which is rather smaller, has shorter and broader wings, white belly and grey foreparts (1). Juvenile more uniformly brown, including all of tail, but has pale band on underwing-coverts and pale panel on inner primaries, often with rufescent nape and large dark ear-coverts patch; bleach very pale by first summer with contrastingly darker head (2); cere and bill grey, legs off-white (1). Adult plumage acquired over 4–5 years, although ragged white tailband may appear as early as at one year old (2); second- to third-year still similar to juvenile, but has more uniformly pale underparts and almost all-dark flight feathers (3). Compared to young H. albicilla is less heavily built, slimmer-headed, longer-tailed and smaller-billed, with diagnostic dark mask, less clearly marked underwing, paler grey-brown upperparts, all-dark tail and rufous-tinged grey-brown underparts that are at most only slightly streaked (1).

Systematics History

Monotypic.

Subspecies

Monotypic.

Distribution

C & S Asia, from S Russia, Kazakhstan (possibly extinct as a breeder (4) ) to Mongolia and NE China, S to Pakistan, N India, Myanmar and SC China (Sichuan).

Habitat

Rivers and lakes, freshwater wetlands and pools; often in arid areas or steppe. In winter, may visit inland seas and in Arabia has been recorded at reservoirs and in littoral habitats (5). Present in high plateaux and valleys, reaching 5200 m in Tibet, and mainly breeds at c. 3200–4700 m in China (6), but is not generally found above 1800 m in Bhutan (7).

Movement

Sedentary and dispersive, although mainly migratory in N, particularly where inland waters frozen over for long periods, e.g. Mongolia is generally vacated by late Sept (6); in Bhutan (7) and N India, some (at least) disperse to highlands post-breeding, e.g. to plateau lakes in W Tibet (1) and in Uttar Pradesh is considered a breeding visitor to Corbett National Park between mid Sept and May (8). In China moves as far SE as Zheijang (6) and Jiangsu in winter (9), with vagrants reaching NW Thailand (most recently in Nov 1999) (6), Cambodia (Jun 2000) (6) and S Vietnam (3) (latter considered doubtful) (6). Possibly recorded in South Korea (6) and some probably also reach Indian Subcontinent (where passage observed through Nepal in Sept/early Oct) (6) and Myanmar, where local populations basically sedentary, for example in Kashmir and most of Pakistan (6). Elsewhere, migrants reach Afghanistan, Arabia, Iran and formerly Iraq, where unrecorded since 1940s (10); only three records in Iran since 1980 (11), whereas in stark contrast all records (some of them involving multiple individuals, both adults and juveniles) in Arabia have been since 1972 (between mid Oct and fourth week of Mar), including one in United Arab Emirates, two in S Oman and ten in SW, E & N Saudi Arabia (5). Pre-1950s, birds even more rarely wandered W to Ukraine, the Crimea, Caucasus and Europe, with single immatures recorded in Poland (in 1943), Norway (1949) and Finland (1926), but an adult seen in Germany, Denmark and Holland in Sept–Oct 1976 is generally considered to have been an escape from captivity (1).

Diet and Foraging

Mainly fish (e.g., in Bangladesh, Cirrhina mrigala, Labio ruhita, Catla catla, Notoptera chitala, Nystus aor, Hilsa ilisha, Ompok pubda, Wallago atu, Amphiomus cuchia) (6); also waterbirds, rodents, lagomorphs, frogs, reptiles (snakes, turtles), insects (wasp larvae) (6), offal and carrion; even human bodies on occasions. Exceptionally recorded killing fish up to 6·5 kg by weight (the latter which it could hardly lift) (6). Observed to kill waterbirds as large as Demoiselle Crane (Anthropoides virgo) and Bar-headed Goose (Anser indicus) (6), as well Pheasant-tailed Jacana (Hydrophasianus chirurgus), Common Poachard (Aythya ferina), Ferruginous Duck (A. nyroca), Lesser Whistling-duck (Dendrocygna javanica) and Little Grebe (Tachybaptus ruficollis) (6), and regularly raids breeding colonies of species such as Black-headed Ibis (Threskiornis melanocephalus), Asian Openbill (Anastomus oscitans) and Darter (Anhinga melanogaster) to take nestlings, as well as those of terns, cormorants, geese and othe, usually ground-nesting, waterbirds, while in winter in India reported to regularly predate Common Coots (Fulica atra) (1) and Ruddy Shelducks (Tadorna ferruginea) (12). Fish caught near surface, without plunge, often in shallows or when stranded in drying pools (6); alternatively taken as carrion; also steals from Ospreys (Pandion haliaetus), Haliastur indus, Circus aeruginosus (1), Icthyophaga humilis, Great Cormorants (Phalacrocorax carbo) (8) and other birds, even terns (6), and in NE India seen to also pirate fish from an otter (Lutra lutra) (13). At least in past, regularly ‘pirated’ wounded ducks shot by hunters (6).

Sounds and Vocal Behavior

Noisy when breeding, but usually silent at other times (9). Loud, guttural and far-carrying “kha-kha-kha-kha” or “gao-gao-gao-gao”, also continuous hoarse “kook-kook-kook” (somewhat like large Larus gull); sometimes utters high-pitched, excited yelping (1). Multiple birds calling simultaneously produce musical babble (2). Each note lasts c. 0·15 seconds, given at rate of 2–3 notes/second (2).

Breeding

Laying Sept–Feb in N India and Myanmar (6), whereas in Bangladesh returns to nest-sites in late Aug (14); later farther N, formerly late Mar in Kazakhstan and May in Tibet, where season lasts until Sept (1). Both adults build (sometimes over period as long as c. 1 month) (6) enormous nest of sticks and branches (up to 200 cm across by > 100 cm deep (1), but perhaps more usually 90–150 cm across by 40–45 cm deep) (6), lined with fresh leaves including those of water hyacinth, rushes and other soft materials (14); normally in large tree (e.g. Bombax ceiba, Ficus infectoria, F. religiosa, Pongamia pinnata, Samanea saman, Tamarindus indica, Terminalia arjuna, Trewia nudiflora) (14) near water (and 4·6 (14)–35 m above ground) (1), but, if necessary, can be built in reedbeds or on ground and, especially in N of range, on cliffs (1); in Bangladesh, where regularly nests in villages, recently observed breeding on large communications towers (14); same nest reused repeatedly, reportedly even for 100 years or more (14). May relay if first clutch is lost early in season (6). Clutch normally 2–3 white eggs, sometimes four or one (6), mean size 69·7 mm × 55·1 mm (3); incubation c. 40 days, mainly by female (provisioned by male), hatching 2–3 days apart (6); chicks have first down brownish grey, second down greyish brown, long and woolly; chicks fed by both adults, but apparently mainly by male (6); normally maximum of two chicks raised to fledging, which takes 70–105 days, with young only becoming independent c. 30 days later (1).

Nest

ENDANGERED. CITES II. Small population, declining as result of habitat loss and degradation and disturbance of wetlands and breeding sites. Global population estimated in 2017 at 1000–2500 mature individuals, a downward revision of the 2000 estimate of 2500–10,000 individuals BirdLife International (2018) Species factsheet: Haliaeetus leucoryphus. Downloaded from http://www.birdlife.org on 09/01/2018. . Possibly no longer breeds in Kazakhstan (where most post-1950s occurrences have been in N & W) (6), although some authorities have noted recent increase in records (15), whereas others consider the species to be still in decline there (16). Main breeding populations thought to be in China and Indian Subcontinent, although numbers apparently always relatively small in Bhutan (7); while in early 2000s Assam population was estimated at < 150 pairs (17). In 2009 surveys in Mongolia produced a minimum total of 20 individuals at eight sites (18), but it is no longer considered a breeding stronghold (and perhaps never was) (19). Recorded from a number of protected areas, especially in Indian Subcontinent, including Corbett National Park (Uttar Pradesh) (8), Kaziranga (20) and Nameri (17) National Parks (Assam), and Manas National Park (Bhutan) (7). Has declined significantly during 20th century in China, Pakistan, India, Nepal and Bangladesh; in Bangladesh, now rarely seen away from NE haors (wetland system), the decline due mainly to loss of large trees and to degradation and overexploitation of wetlands, as well as other human factors, although local conservation initiatives appear to be having some success (14). Main threats are habitat loss, degradation and disturbance. In Indian Subcontinent, and probably through most of range, wetlands drained or converted for agriculture and human settlements, while felling of large trees close to wetlands has reduced availability of nest-sites and roosting sites; spread of water hyacinth (Eichhornia crassipes) a big problem in India, as is siltation of lakes (caused by deforestation). Moreover, breeding success reduced by pesticide pollution of wetlands and contamination of wetlands by industrial effluents, and this compounded by disturbance of wetlands. Reductions in prey, due chiefly to hunting and overfishing, are further human-related problems. Development of oil and gas fields a threat in Myanmar, and hunting a problem locally in China. In Mongolia, in summer 2009, two recently completed hydroelectric dams were found to be severely disrupting water levels in drainage basins and could have adverse impact on all sites where this species occurs in Great Lake Basin, while overfishing noted at several sites and falling water levels (caused by low rainfall) observed in some areas (18).

Distribution of the Pallas's Fish-Eagle - Range Map
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  • Year-round
  • Migration
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  • Non-Breeding
Distribution of the Pallas's Fish-Eagle

Recommended Citation

Orta, J., D. A. Christie, G. M. Kirwan, and C. J. Sharpe (2020). Pallas's Fish-Eagle (Haliaeetus leucoryphus), 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.pafeag1.01
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