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Japanese Night Heron Gorsachius goisagi Scientific name definitions

Albert Martínez-Vilalta, Anna Motis, and Guy M. Kirwan
Version: 1.0 — Published March 4, 2020
Text last updated March 17, 2018

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Field Identification

48–49 cm; 527 g (one male); wingspan 87–89 cm (1). Similar to G. melanolophus, but lacks black cap and long crest, has darker drabber brown head , neck and upper body (richer chestnut-brown in G. melanolophus) (2); flanks less mottled and remiges  lack white tips (3); bill shorter and stouter. Bill possibly all green-black during breeding season, otherwise dark brown on upper mandible with yellow lower mandible (3); facial skin changes from yellow to blue in breeding season (3); iris  pale yellow with yellowish-green orbital ring (1); tarsi dark yellowish green (1). Juvenile  has crown blackish or dark brown and is less rufous on rest of head ; neck more spotted and streaked chestnut, wing-coverts paler and tipped buff (forming obvious wingbar in flight), undertail-coverts white, and has off-white lores and yellow eyering (1, 4).

Systematics History

Probably most closely related to G. melanolophus. Monotypic.

Subspecies

Monotypic.

Distribution

Breeds in S Japan on Honshu, Shikoku and possibly Kyushu; recently found breeding in Jeju Is, S Korea (5); one breeding report from Taiwan, and has been recorded in spring and summer in Russia (Primorye and Sakhalin). Winters from Ryukyu Is to Philippines.

Habitat

Rivers and swamps in thickly forested areas, also farms and rice paddies (3) and bamboo forest on migration (3), and in lightly wooded areas close to cultivation in winter (6), generally occurring in low parts of mountains from 50 m to 240 m, although it has been reported to 1100 m in Indonesia (7), 1500 m in Japan and generally to 1350 m in the Philippines, with two records on Luzon from as high as 2400 m (3). Habitual skulker in dense undergrowth.

Movement

Some birds sedentary, but vast majority of population seems to migrate S in Sept/Oct, returning in early Apr, although Mar records exist for Honshu  . Main wintering area appears to be Philippines, but also recorded as non-breeding visitor to Indonesia, rare winter visitor and passage migrant on Taiwan (2), and vagrant to Brunei (Oct 1985 (8), with perhaps same bird again Nov 1988) (9), Sulawesi, Halmahera, Seram (Jul 2013) (7) and Sumatra (Feb 2004) (10), with single record on Palau, in W Caroline Is (Jan 1932) (11). Improved awareness of identification criteria for immatures has led to a marked increase in records from Philippines. Record of exceptionally early migrant on Palawan (Philippines) on 5 Aug, which in following year was recovered in S Honshu (Japan) on 28 Apr, while there is also another Philippine record, from Mindanao, dated 14 Aug (12). All other records in Philippines dated Oct–May (11), although it has been suggested that some occasionally summer there (3). Occasional records to N of breeding range on Hokkaido and Sado (N Japan), and also Primorye and Sakhalin (off SE Ussuriland), mainly in spring (especially May) (11). Sometimes diurnal during migration, when recorded also in Hong Kong and in coastal mainland China (mainly late Apr to mid May, and Nov) (11).

Diet and Foraging

Very little known. Apparently mainly crabs and other crustaceans; also insects, ground and scarabid beetles, earthworms (3), snails, cicadas and small fish; perhaps also small reptiles and a loach (Paramisgurnus dabryanus) has also been recorded (4). Diet at nest in South Korea included adult insects and larvae (Graptopsaltria nigrofuscata and Gryptotympana dubia, Cicadidae, Pterostichus sp. and Nicrophorus sp., Carabidae), earthworms (Lumbriculida sp.) and snails (mainly Nesiohelix samarangae) (13). Walks slowly along watercourses or around pools, but also forages on dry ground  , rarely in open (3). In a study in Japan, land snails, freshwater crabs, ground, and scarabid beetles were the major prey items found in the pellets, whereas no fish were detected, indicating that the birds mainly forage on soil animals on the forest floor (14). Solitary or in small, loose flocks. Generally nocturnal or crepuscular (3), but sometimes feeds during day when conditions are dull and cloudy.

Sounds and Vocal Behavior

Gives croaking “buo, buo” when feeding or at nest (3), slow, repetitive and somewhat owl-like, mainly given early evening and sometimes on migration; also rendered “bwoo bwoo bwoo” (1).

Breeding

Very little known. Eggs recorded in May–Jun and Jul (latter perhaps second or replacement clutch) (11). Solitary or in small groups. Nests in dense foliage 7–20 m above ground (mean 10·6 m in 16·5 m high trees in recent Japanese study) (15), with more than 40% in Prunus spp. in one study (15), but also conifers (cedars Cryptomeria, cypresses Chamaecyparis) (3), and other deciduous trees (oaks Quercus, zelkovi Zelkova and chestnut Castanea) (3); once mulberry (Morus bombycis) (13); nests sometimes in relatively close proximity (250–500 m) (3) and appears to prefer to nest at bottom, or on lower slopes, of valleys (15); nest is flimsy stick platform on more or less horizontal branch (3), typically 1–4 m from main trunk (11). One Korean nest was constucted mainly of sticks from following trees, Styrax japonica, Cryptomeria japonica and Morus bombycis (13). Clutch 3–4 dull white (3) eggs, size 47·5 mm × 37 mm (3); incubation 17–27 days, by both sexes (11); fledging 35–37 days (once 42 days) (13); feeding rates apparently vary, at Korean nest 5–6 times daily 30 days after hatching, and twice daily 35 days after hatching (13).

ENDANGERED. Overall population estimated at 600–1700 individuals within an overall range of 35,800 km², but this may be an underestimate. Only six confirmed and 15 possible breeding sites in Japan (3), where considered uncommon to rare and very local throughout, and suitable habitat now extremely scarce as a result of deforestation and conversion to plantations (3); it was apparently locally common in Japan until 1970s, but by the 1980s and 1990s had disappeared from many former breeding sites (3). Little information available on status and general biology, due mainly to dense, tangled habitat, together with nocturnal habits, but 26 nests were found in West Mikawa area of Aichi Prefecture in 2009–2010 (15). Marked decline in last 30 years, to which hunting and introduced predators (e.g. Siberian weasal Mustela sibirica) (11) may also have contributed (3); in 1957 still considered not uncommon on Miyake jima, to S of Tokyo; seems to have been relatively common in places at beginning of century, as eggs and skins were sold cheaply; one such site was near what is now Tokyo’s main airport. None recorded in Asian Waterfowl Census, Jan 1990. Recently discovered breeding once in Taiwan (3) (perhaps regularly) (16) and on Jeju I off South Korea (13). Uncommon winter visitor to Philippines, where deforestation must also be considered primary threat (3), but records increasing due to better knowledge of species’ non-adult plumages and the archipelago appears to its main wintering area; just four records on Sulawesi and two on Halmahera (11). Apparently just two records from mainland China since early 1960s, one of two birds at Wuyuan in Jiangxi Province in Apr 2006 and a taxidermy specimen in Haiyan county, Zhejiang province, in Feb 2010 and apparently purchased in Haining city in Apr 1998.

Distribution of the Japanese Night Heron - Range Map
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  • Year-round
  • Migration
  • Breeding
  • Non-Breeding
Distribution of the Japanese Night Heron

Recommended Citation

Martínez-Vilalta, A., A. Motis, and G. M. Kirwan (2020). Japanese Night Heron (Gorsachius goisagi), 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.janher1.01
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