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Chinese Pond-Heron Ardeola bacchus Scientific name definitions

Albert Martínez-Vilalta, Anna Motis, and Guy M. Kirwan
Version: 1.0 — Published March 4, 2020
Text last updated June 3, 2017

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Field Identification

c. 42–52 cm (1); 280–332 g (2); wingspan 79–90 cm (1). Much darker than breeding-plumaged Bubulcus ibis, but main confusion risk is with closely related A. speciosa, from which it is distinguished in breeding plumage by darker head and upper breast, and has rufous crest plumes (not whitish buff). Upper back has long blackish plumes  that extend beyond tail, while the wings, rest of upperparts, throat and belly  are white, while breast has long maroon plumes and there are long dark grey plumes on the pectoral region. Female reported to differ from male in paler foreneck, shorter plumes, lack of slaty patch on breast and browner scapulars and tertials. During courtship legs become intense pinkish red, at other times yellowish; bill  yellow with bluish base and black tip in breeding season (maxilla dusky in non-breeding season), eyes golden-yellow and facial skin greenish yellow (including pale eyering). Non-breeding adult similar to congeners, but has darker back and tips to primaries than smaller-bodied, smaller-billed and shorter-winged A. speciosa; compared to A. ralloides has darker (not tawny-brown) back and lack of any suggestion of black streaking on head and crest. Juvenile brown, heavily streaked buff and dark brown, underparts whitish with heavy brown streaking, while presumed first-winter plumage has streaked lesser wing-coverts (versus plain white in adults) and more extensively brown outer primaries and tail tip (3). First-summer plumage reported to be very similar to that of adult, albeit perhaps duller overall with some streaking on head and neck (4).

Systematics History

Closely related to A. ralloides, A. grayii and A. speciosa. Perhaps also close to A. idae. Monotypic.

Subspecies

Monotypic.

Distribution

Breeds from Russian Far East, NE & E China and Japan SW to NE India (Assam) and N Myanmar. Winters in Andaman Is, Malay Peninsula, Indochina, Borneo and Sumatra, and NE to Ryukyu Is.

Habitat

Frequents paddyfields, swamps, ponds, riverbanks; also in mangroves and at tidal pools, mainly in lowlands. In N Thailand recorded on streams up to 1450 m (5); in dry grassland in Hong Kong and Thailand. In SW China, recorded to at least 4000 m (on migration), with vagrant records elsewhere in the Himalayas as high as 3570 m (6, 7).

Movement

Indian and N Indochinese birds considered sedentary, with some local movements, but former might in fact be migrants (as breeding apparently never proven) (8). N populations migratory: Chinese birds leave breeding grounds in Aug/Oct (e.g. passage through Hebei, NE China, observed late Aug to mid or late Oct) (9), returning in Mar/Apr, when occasionally overshoots to South Korea, Japan (e.g. N Hokkaido) (10) and elsewhere in N China (Heilongjiang and Xinjiang) (1); occurs in Malay Peninsula Sept–May (3), S Nansei Shoto (Japan) Oct–Apr (1), and in Borneo Sept–Feb (extreme dates early Sept and late May) (11). Occasional in Taiwan and on Andamans (8), with 13 records in Philippines (Luzon, Mindoro, Negros and Palawan; Oct–Apr) (12, 13, 14, 15); vagrant to L Baikal, Siberia (Jun 1998) (16), Alaska (Pribilofs, Aug 1996; Attu I, May 2010; St Lawrence I, Jul 2011) (4), Guam (Feb–Apr 1987) (17), S & NW India (Gujarat, May 1980; Tamil Nadu, Mar–Apr 2013 (18); Rajasthan, Jun 2013) (19), Bhutan (May 2013), Sri Lanka (8), Pakistan (Jul 2011) (7) and Oman (Aug 2010, Sept 2012) (20). Records in E Indian Ocean and Australia, on Cocos Is (May 2006, 40575  ), Christmas (Mar 2008, 40695  ) and near Broome (Western Australia) in 39508  , plausibly all pertain to natural vagrants. However, single adults in Norway, autumn 1973, and Hungary, Aug 2000 (21), until recently usually considered to be genuine vagrants, are now regarded as being probable escapes, as were single adults in Finland in 39264  and 41122  , but singles in S & SE England in Oct–Nov 2004 (22) and Jan–Mar 2014 have recently been accepted as natural vagrants (23).

Diet and Foraging

Small frogs  , worms, aquatic invertebrates, fish, molluscs, worms (24), some terrestrial insects and even small birds (24). Little known about technique, but probably most commonly Standing and Walking Slowly , as well as Feet First Diving, Hovering (25) and Dipping (24); in Hong Kong recorded diving into ponds from overhanging perches up to 10 m high, they also feed on the wing and have been observed feeding commensally with otters (Lutra) (24). Also in Hong Kong noted feeding more around dawn and dusk than in rest of day, although other records indicate regular feeding during day. Solitary or in pairs, sometimes in small flocks of up to six birds, more occasionally up to 60 (24).

Sounds and Vocal Behavior

Vocalizations poorly documented, although usually considered to be rather silent in non-breeding season, other than a gruff “kwa” on being flushed, similar to other Ardeola (1).

Breeding

In India, May–Aug; in China, nest records from Apr–Jul (24); in Hunan (SC China), lays in early May. Colonial, normally forming small colonies, sometimes with other herons, especially Egretta garzetta and night-herons (Nycticorax) (24); in extreme W of range can breed alongside A. grayii. Usually nests high in trees (e.g. Populus, Sophora, Quercus, Ulmus, Ficus, Cunninghamia and Sassafras) (24), c. 17 m up on average at Ichang (E China) and in another study > 50% of nests were sited above 10 m (24); also nests in bamboos (e.g. Pleioblastus simonii) and mangroves (26); small stick nest sometimes lined with leaves and grass. Double-brooded, with second clutch typically laid after young from first clutch have become independent (24). Normally 4–6 greenish-blue eggs (2–8), mean size 37·7–39 mm × 28·4–29·7 mm (24); incubation 18–22 days by both adults (24); fledging c. 30 days and become independent six days later (24). Mynas (Acridotheres) may steal food from chicks (24). No additional information.

Not globally threatened (Least Concern). Global population estimated at 25,000–1,000,000 individuals. One of commonest herons in E China, with breeding densities of up to 1401 birds/km² and more than 6000 nests have been discovered at just two sites (24); colony of 100–150 pairs in Hong Kong, where loss of fishpond habitat has led to recent decline (24). In winter, common in Malay Peninsula, with 577 counted in Jan 1990; very common in Vietnam and also in Thailand, where 1320 recorded in Jan 1990; apparently declining visitor to Borneo in recent years. Records increasing in Japan, where has bred on several occasions since 1981 (27). Rare in NE Indian Subcontinent, with no definitive evidence of breeding (8, 28). Large quantities of eggs and birds taken in parts of China for food; nonetheless, seems to have been expanding range during 1980s.

Distribution of the Chinese Pond-Heron - Range Map
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  • Year-round
  • Migration
  • Breeding
  • Non-Breeding
Distribution of the Chinese Pond-Heron

Recommended Citation

Martínez-Vilalta, A., A. Motis, and G. M. Kirwan (2020). Chinese Pond-Heron (Ardeola bacchus), 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.chpher1.01
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