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Crested Serpent-Eagle Spilornis cheela Scientific name definitions

William S. Clark, Jeffrey S. Marks, and Guy M. Kirwan
Version: 1.0 — Published March 4, 2020
Text last updated January 30, 2016

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Field Identification

50–74 cm (cheela), 50–56 cm (perplexus); 420–1800 g (palawanensis 688 g males, 853 g females 1; pallidus 675–925 g); wingspan 109–169 cm (cheela), 110–123 cm (perplexus). Small to fairly large dark brownish eagle ; size extremely variable; shoulders and undersides (especially belly, thighs and undertail-coverts) variously marked with white spots or barring. Females average 4–6% larger than males, but up to 17% larger in some subspecies 2. Short, rounded dark crest and broad wings characteristic; prominent pale band in tail and along trailing edge of underwing present distinctive pattern in flight. Juvenile paler with black face patches and two pale tailbands. Racial variation mainly in size and colour: nominate race largest, minimus smallest; island forms (e.g. <em>spilogaster</em> , <em>perplexus</em> ) tend to be smaller, some only half the size of nominate cheela; birds from wetter habitats (e.g. <em>abbotti</em> , bido) tend to be darker; ricketti averages larger than burmanicus, has paler underparts, narrow whitish bars on breast, and fewer bars/spots over rest of underparts. .

Systematics History

Editor's Note: This article requires further editing work to merge existing content into the appropriate Subspecies sections. Please bear with us while this update takes place.

Closely related to S. holospilus, S. klossi, S. kinabaluensis and S. rufipectus, and may be conspecific with any or all of these taxa. Races perplexus, minimus, abbotti, asturinus, sipora, natunensis and baweanus have recently been treated as valid individual species 3, but none of these appears to fulfil the required criteria for species status when compared with all other taxa in the complex, even though the nearest neighbour may be very different; for the moment, therefore, pending a more detailed and comprehensive analysis, these taxa are retained as subspecies of S. cheela. Situation in Nicobar Is somewhat complicated, although presence of two different species of Spilornis generally agreed upon: C Nicobars form minimus, when treated as a full species, often considered to include S. klossi as a race, but minimus is closer to other forms of S. cheela group 4; an undescribed form of present species (based on three specimens) in S Nicobars was previously thought to be of race malayensis, but clearly distinct from latter and from sympatric klossi 4. Several further races have been described, e.g. tonkinensis (from N Vietnam), but considered invalid. Twenty-one subspecies currently recognized.

Subspecies


EBIRD GROUP (POLYTYPIC)

Crested Serpent-Eagle (Crested) Spilornis cheela [cheela Group]


SUBSPECIES

Spilornis cheela cheela Scientific name definitions

Distribution
extreme NE Pakistan (rare) (5) and N India E to Nepal, Assam and NE and C Bangladesh; winter visitor in Gangetic Plain.

SUBSPECIES

Spilornis cheela melanotis Scientific name definitions

Distribution
peninsular India S from Gujarat and Gangetic Plain.

SUBSPECIES

Spilornis cheela spilogaster Scientific name definitions

Distribution
Sri Lanka.

SUBSPECIES

Spilornis cheela burmanicus Scientific name definitions

Distribution
Myanmar, S China, Thailand and Indochina.

SUBSPECIES

Spilornis cheela ricketti Scientific name definitions

Distribution
SC and SE China and N Vietnam.

SUBSPECIES

Spilornis cheela hoya Scientific name definitions

Distribution
Taiwan.

SUBSPECIES

Spilornis cheela rutherfordi Scientific name definitions

Distribution
Hainan.

SUBSPECIES

Spilornis cheela palawanensis Scientific name definitions

Distribution
W Philippines (Calamian Is and Palawan group).

SUBSPECIES

Spilornis cheela pallidus Scientific name definitions

Distribution
lowlands of N Borneo.

SUBSPECIES

Spilornis cheela richmondi Scientific name definitions

Distribution
S Borneo.

SUBSPECIES

Spilornis cheela malayensis Scientific name definitions

Distribution
Malay Peninsula (from S Tenasserim), Anambas Is (off E Peninsular Malaysia) and N Sumatra.

SUBSPECIES

Spilornis cheela batu Scientific name definitions

Distribution
Batu Is (off W Sumatra) and mainland S Sumatra.

SUBSPECIES

Spilornis cheela bido Scientific name definitions

Distribution
Java and Bali.

EBIRD GROUP (MONOTYPIC)

Crested Serpent-Eagle (Andaman) Spilornis cheela davisoni Scientific name definitions

Distribution

Andaman Is.

EBIRD GROUP (MONOTYPIC)

Crested Serpent-Eagle (Central Nicobar) Spilornis cheela minimus Scientific name definitions

Distribution

C Nicobar Is.

EBIRD GROUP (MONOTYPIC)

Crested Serpent-Eagle (Ryukyu) Spilornis cheela perplexus Scientific name definitions

Distribution

S Ryukyu Is (Miyako Is, Yaeyama Is).

EBIRD GROUP (MONOTYPIC)

Crested Serpent-Eagle (Natuna) Spilornis cheela natunensis Scientific name definitions

Distribution

N Natuna Is (off W Borneo) and Belitung I (off SE Sumatra).

EBIRD GROUP (MONOTYPIC)

Crested Serpent-Eagle (Simeulue) Spilornis cheela abbotti Scientific name definitions

Distribution

Simeulue I (off W Sumatra).

EBIRD GROUP (MONOTYPIC)

Crested Serpent-Eagle (Nias) Spilornis cheela asturinus Scientific name definitions

Distribution

Nias I (off W Sumatra).

EBIRD GROUP (MONOTYPIC)

Crested Serpent-Eagle (Mentawai) Spilornis cheela sipora Scientific name definitions

Distribution

Mentawai Is (off W Sumatra).

EBIRD GROUP (MONOTYPIC)

Crested Serpent-Eagle (Bawean) Spilornis cheela baweanus Scientific name definitions

Distribution

Bawean I (off N Java).

Distribution

Also occurs (race undescribed) in S Nicobar Is (Menchal, Kondul, Great Nicobar) 6.

Habitat

Present in a wide variety of tropical and subtropical forest habitats, including dry to wet primary forest, riparian gallery forest, savanna, mangroves, degraded semi-open mixed forest, tea and teak plantations, and edges of cultivated areas and villages. Typically avoids dense forest interior; prefers secondary or partly open forest, clearings, gaps and forest edge. Preference for edge and more-open forest reflected by increased abundance with logging in SE Sabah on Borneo (7). Home-range size of radio-tagged birds in Taiwan averaged 12·3 km² using minimum convex polygon method (8). Race perplexus of Ishigaki and Iriomote Is, Japan, unusual in favouring wet grassland habitat, in addition to forest edge (9). Occurs mostly from sea-level to 2000 m, occasionally as high as 3000 m or more in Bhutan and Nepal (10, 2).

Migration Overview

Usually considered sedentary aside from juvenile dispersal, but birds that clearly were northbound migrants observed in S Thailand in Mar 2007 and 2008 11.

Diet and Foraging

Feeds mainly on reptiles, especially tree snakes ; less commonly on mammals, crabs, eels, frogs and birds. Recent study in India documented 173 prey items: 74% reptiles, 18% birds, 7% amphibians and 0·5% each fishes and mammals 12. Another study in India recorded predation on termites 13, and in Peninsular Malaysia has been observed hunting large earthworms 14. Hunts almost exclusively from exposed perch near open glade or along stream or forest edge; when foraging remains still for long periods while scanning for suitable prey items. Prey taken on ground or from trees, after short stoop, and consumed on ground or on elevated perch .

Sounds and Vocal Behavior

Fairly noisy, especially during aerial displays in breeding season; also vocalizes while perched. Most common call a loud, shrill “pi-pi-wheeeah-wheeah”  , the introductory notes often inaudible from a distance 2. Much time spent soaring and calling throughout year.

Breeding

Nesting chronology varies with locality, depending on elevation, latitude and timing of rainy season (laying mostly in dry season in N of range): Dec–Mar in S India; Feb–May in N India and Sri Lanka; Feb–Apr in Burma and Sumatra, Feb–Nov in Java; record of second brood in Jun in Burma. Nests 55–105 cm across, 10–30 cm deep; lined with grass and green leaves; built by pair 6–25 m above ground in large tree; often near clearing or stream. Sometimes breeds in old nests of other raptors, e.g. Gyps bengalensis and Nisaetus cirrhatus 15. Spectacular display flights include mutual soaring, undulations and threat display, with wings bowed upwards and head and tail raised; all accompanied by loud vocalizations. Clutch one egg (reports of two eggs should be verified); incubation c. 40 days (range 37–42 days), by female only; nestling period c. 64 days (range 59–65 days) 12. Hatchling has white down; both adults feed chick; post-fledging dependency period unknown. Fledgling seen being fed in Sept in Malaysia, suggesting a late nesting or long dependency period.

Not globally threatened (Least Concern). CITES II. Throughout extensive range generally widespread and common, sometimes abundant, but locally uncommon. No threats known at present, and species appears to be quite adaptable to habitat disturbance, including logging that opens up dense forest. Surveys are needed to determine conservation status of well-marked island races, especially because many (all?) may prove to be distinct species that would have small global ranges and population sizes. For example, race natunensis went completely unrecorded between 1937 and 2014, when it was observed several times on Belitung I in somewhat degraded habitat, and this taxon is suspected to be threatened by tin mining, loss of habitat (to explanding oil-palm plantations) and infrastructural development 16. Study of radio-tagged birds in S Taiwan found density of 2·7 individuals/km² 8. Using average of only one pair/100 km² yields population estimate of 160,000–180,000 adults for all currently recognized subspecies 2.

Distribution of the Crested Serpent-Eagle - Range Map
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Distribution of the Crested Serpent-Eagle

Recommended Citation

Clark, W. S., J. S. Marks, and G. M. Kirwan (2020). Crested Serpent-Eagle (Spilornis cheela), 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.crseag1.01
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