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Yellow Bittern Ixobrychus sinensis Scientific name definitions

Albert Martínez-Vilalta, Anna Motis, and Guy M. Kirwan
Version: 1.0 — Published March 4, 2020
Text last updated November 27, 2015

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Field Identification

30–40 cm; 81–104 g (1, 2, 3); wingspan 45–53 cm (4, 5). Male has dull black to blue-grey crown  and crest, brown forehead, sandy-brown throat streaked brown, buff neck-sides, rufous to sandy-brown back, often with pinkish to maroon wash, pale wing-coverts contrasting with blackish flight feathers  , grey underwing with pale coverts, sandy-brown underparts and black tail; long, thin, ivory-coloured bill , with darker maxilla and red base in courtship, yellow eyes, yellow-green lores and legs. Female  has indistinctly streaked crown  , rufous hindneck and upper back, dark red-brown and buff-streaked underparts, with black on breast-sides, chestnut-buff streaking on throat and darker wing patches than male. Separated from slightly larger and shorter-billed I. minutus by brown (not black) back and yellow-buff (not grey-buff to white) wing patches (they breed synptopically in SW Oman), while present species is separated from marginally larger I. eurhythmus by paler upperparts and more contrasting upperwing, while from juvenile of latter species it is distinguished by lack of pale spotting on upperwing; from I. cinnamomeus by slightly smaller size and tawny-brown (not cinnamon) general coloration. Juvenile  browner, lacks dark crown but is obviously streaked over head, back and underparts (being the most obviously streaked Ixobrychus at this age) and shows less contrast between pale wing patches and dark flight feathers than I. minutus at any age (6); bill has dark maxilla and yellow mandible, legs olive-yellow and eyes yellow. Probably achieves adult plumage in second year.

Systematics History

Closely related to I. exilis, I. minutus and I. dubius. Monotypic.

Subspecies

Monotypic.

Distribution

Oman; Seychelles; Indian Subcontinent, SE Russia and Japan through C & E China and Taiwan to SE Asia, Greater and Lesser Sundas, Philippines, New Guinea (possibly), N Solomons (Bougainville) and W Micronesia. N populations migrate to S of range, to S India, Philippines and Indonesia, some reaching Wallacea and New Guinea.

Habitat

Mostly in freshwater marshes ; also reedbeds and other dense aquatic vegetation fringing lakes, in riverside shrubs, inland swamps, rice paddies and flooded fields; in parts of China occurs in mangroves. From lowlands into hills, occurring up to 900 m in India, 1200 m in Sri Lanka and 1500 m in Sumatra.

Movement

N populations (S to C China and those in NW India) migrate to S of range, to Philippines and Indonesia, some birds reaching Wallacea (e.g. Alor (7) and Kai Is) (8) and New Guinea; leave in Oct and return in mid Apr to late May (2). Passes through Thai-Malay Peninsula Oct–Dec (mainly Nov) and Mar–Apr, with apparent faithfulness to winter and staging sites proven by retraps in subsequent seasons (9). Migration takes place by night. S populations (including some of S Japan, S China, N Burma and N Indochina) sedentary. Resident in NE India (Assam, Cachar, NW Maharashtra), E Bangladesh and Sri Lanka, with some local movements related to water conditions; however, those breeding in NW Indian Subcontinent (from Indus Valley of Pakistan E to Gangetic Plain) move S in winter as far as Sri Lanka (6). Perhaps mainly summer visitor to SW Oman (late Apr to late Nov), although records are available from all months (10). Long-distance migration has permitted colonization of remote Pacific islands and Seychelles (where perhaps only vagrant on Aride and Curieuse) (11). Accidental to Maldives (12), Chagos Is (annual), Lakshadweep Is, mainland Australia (Queensland and Western Australia) (2), Cocos  (Keeling) Is and Christmas I  (Indian Ocean) (13), with single record in North America, in Alaska (Attu I, W Aleutians) in May 1989 (14). A record from S England, in Nov 1962, is considered to have been correctly identified, but has not been accepted (15).

Diet and Foraging

Mainly aquatic insects and their larvae (e.g. Diptera, Libellulidae, Coenagrionidae, Diplonychus japonicus) (16); also small fish (e.g. loaches, Carassius auratus, Trichogaster, Misgurnus anguillicaudatus, Pseudorasbora parva) (9, 2, 16), crustaceans  (crayfish and freshwater prawns) (2), frogs (e.g. Hyla arborea) (16), molluscs, crickets, lizards (17). In Malaysia, compared to I. cinnamomeus, appears to take more terrestrial invertebrates (52% of diet versus 41%), with other main constituents of diet fish (16%) and amphibians (4%), and 28% unidentified (18). Sometimes catches flies in flight (Standing Flycatching). Solitary and secretive, typically forages by Standing and Walking Slowly, but also Gleaning, Running and Hopping (2); mainly crepuscular and nocturnal, but sometimes active on overcast days.

Sounds and Vocal Behavior

Following vocalizations have been described: soft, repetitive, up- and downslurred “oo-oo-oo” or “crrw, crrw”, given at rate of c. 1 note per c. 2 seconds, in display, territory defence, advertisment, and with large young, by day or night (likened to Geopalia dove, but more continuous and monotonous), a staccato, dry “kakak, kakak” or “kik-kik-kik” in flight  , a loud, repeated guttural grunting “ohr” and a similar call, albeit much softer, when arriving at nest with food (2, 6).

Breeding

Starts spring in N, May–Aug in Egypt (19), Japan and China (2); Jun–Sept in India, related to monsoons; young recorded May–Nov in SW Oman (20); laying mainly Jul–Oct in Malay Peninsula (but nests with eggs or young found all months except Jan–Mar) (9); Feb–May in Philippines (4); May on Sumbawa (Indonesia); Sept and Jan in Seychelles (11); Sept–Apr in Solomon Is; Feb on Saipan (Mariana Is) (17). Normally solitary, but can form small groups at favourable sites (21), with up to six nests reported in same tree but little or no synchronicity within colony (2). Mean nesting density of 11·4 pairs/ha reported in China, but up to 31·18 pairs/ha in irrigated rice fields (2). Nests usually less than 3 m (9) above water or mud, in bushes or herbaceous plants within reeds, grass, cattails, bulrushes, wild sugarcane or bamboo, or in mangroves, occasionally taller trees (e.g. Ficus and mangos), often near rice paddies and usually close to open water (2); nest slight platform of grass and leaves, 145–250 mm in diameter, 60–110 mm thick and 60–110 mm tall (21), usually with canopy of foliage and constructed by female (2). Reported to be sometimes double- or even triple-brooded (2). Normally 4–6 greenish-white or greenish-blue eggs (3–7), laid at one-day intervals, mean size 30–33 mm × 23–24·5 mm (2); incubation c. 17–20 days (21), by both sexes, commencing with first egg (9, 2); chicks hatch asynchronously and have pinkish down, yellow eyes and other bare parts pale yellow-green (9); start to clamber about nest at c. 15 days and abandon it completely at 20 days (2). Inter-specific parasitism reported in Japan, where Common Moorhens (Gallinula chloropus) laid eggs in 3% of nests of present species (2). No further information.

Not globally threatened (Least Concern). Common to frequent in many areas, e.g. Pakistan, Japan, Thailand, Borneo (winter) and Philippines , where generally considered commonest of small bitterns (2), but apparently rare in parts of Indochina (e.g. Cambodia) (22); 176 counted in China, c. 1400 at L Tempe, S Sulawesi, Jan 1990. Breeding range in Malay Peninsula spread S to Singapore in 1980s (9). However, precise breeding range further E very unclear, e.g. probably breeds in Sarawak, Brunei and Kalimantan (Borneo, where mainly a winter visitor) (23, 24), recently confirmed to be resident (and probably breeding) on Timor (and probably so on Bali and Sumba) (25, 7), with one record of nesting on Sumbawa, and is even known to breed on Bougainville (Solomon Is), but not elsewhere in Melanesia (26). Population on Saipan (Mariana Is) most recently estimated at c. 1400 birds and has increased substantially since 1982 (27). Extralimital to main range: species first recorded in SW Oman in 1984, but presence not confirmed until 1997 (28) though now known to breed at several sites and recorded at several localities in N Oman (20, 10); first definitely recorded on Socotra (Yemen) in Nov 1999 (29), where perhaps breeds but unproven to date, with records in Jan, May and Oct–Dec (20); even more recently (Apr 2012) discovered breeding at three mangrove sites in SE Egypt (30, 19, 31), with an addition claim from the Nile Valley (32), and a record of two individuals at a mangrove in Djibouti in Jan 2014 (33). In China and upland Borneo protected and considered beneficial by rice growers, as it eats stem-boring crickets in paddyfields. Considered rare and local in Melanesia (26). Population of Seychelles estimated at under 100 pairs at end of 1970s and 228 birds in 1990–2000, declining due to habitat destruction for agriculture and infrastructural developments (11).

Distribution of the Yellow Bittern - Range Map
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  • Year-round
  • Migration
  • Breeding
  • Non-Breeding
Distribution of the Yellow Bittern

Recommended Citation

Martínez-Vilalta, A., A. Motis, and G. M. Kirwan (2020). Yellow Bittern (Ixobrychus sinensis), 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.yelbit.01
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