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Nankeen Night Heron Nycticorax caledonicus Scientific name definitions

Albert Martínez-Vilalta, Anna Motis, and Guy M. Kirwan
Version: 1.1 — Published August 18, 2021

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Field Identification

55–65 cm; 550–1014 g (1); wingspan 95–116 cm (2). Medium-sized, stocky, short- and thick-necked heron, with short, heavy, black bill . Distinctive combination of black cap and rufous to dull brown back and wings . Very variable, even within same area; sexes alike, though female averages smaller in most measurements. Overall coloration pale cinnamon to deep brown (offering ready distinction from adult N. nycticorax), paler on neck and throat, with white belly (in most subspecies) and in breeding plumage has two or three long white plumes (initially tipped black) emanating from crown; underwing white with cinnamon-rufous flight feathers ; legs range from bright yellow to dusky ochre-yellow, eyes  yellow, and lores and facial skin greenish yellow. Legs can be bright pink, lores blue and iris brilliant red during courtship. Non-breeding adult lacks nuchal plumes. Juvenile heavily spotted and streaked rufous, brown, buff and white, underwing white streaked grey-brown and rufous-brown flight feathers; eyes yellow to orange-yellow, facial skin yellow-olive, legs and feet lime-green to olive-grey, and bill mainly grey-black with yellowish cutting edges and base to mandible; with age crown becomes blacker and upperparts more rufous and less spotted. Young of this species difficult to separate from same-age N. nycticorax, but note more rufous-brown tone to plumage, dark brown-buff (not brown) and spotted uppertail-coverts, white (not grey-brown) rump, rufous-brown barred dark brown (not grey) tail and, on average, slightly smaller size. Compared to juvenile Butorides striata, present species is larger, has obvious pale spotting on back and wings, and pale underparts; from Botaurus poiciloptilus by shorter neck, hunched posture, rufous (not brown) upperparts, spotted (not barred) wings and habitat. Races separated on colours of upperparts and of nuchal plumes, with intergrades between australasiae and manillensis reported from Java and Borneo, and between australasiae and mandibularis in New Britain and New Hanover (1, 3); nominate has duller and greyer upperparts compared to adjacent subspecies; <em>manillensis</em> is relatively large and dark, with dark maroon-coloured upperparts and chestnut-washed underparts, poorly developed eyering and nuchal plumes are smoky black or white with dusky bases and tips; australasiae is smaller and paler than the previous race, and has a superciliary and pale rufous-chestnut upperparts, lacking the dull tones of the nominate (4); mandibularis is relatively small race, lacks rufous-white eyebrow and eyering, but has rich chestnut upperparts, neck and upper breast, and black-tipped nuchal plumes; <em>pelewensis</em> is dull maroon above.

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 N. nycticorax, with which known to have hybridized in Java, Sulawesi and Philippines. Race australasiae previously listed as hilli, but former has priority. Proposed race major (C & S Philippines) is included in manillensis. Five extant subspecies recognized.

Subspecies

Also New Zealand, where introduced (australasiae), but possibly also native (5).


SUBSPECIES

Nycticorax caledonicus crassirostris Scientific name definitions

Distribution

Bonin Is.

SUBSPECIES

Nycticorax caledonicus manillensis Scientific name definitions

Distribution

Philippines, Borneo, Java and Bali.

SUBSPECIES

Nycticorax caledonicus australasiae Scientific name definitions

Distribution

Sulawesi, Moluccas, Lesser Sundas and Aru Is through W Papuan Is and lowland New Guinea (including Biak I) to NW Bismarck Archipelago (Ninigo Is to Admiralty Is) and Australia (except arid interior).

SUBSPECIES

Nycticorax caledonicus mandibularis Scientific name definitions

Distribution

Bismarck Archipelago (except NW islands) to Solomon Is.

SUBSPECIES

Nycticorax caledonicus pelewensis Scientific name definitions

Distribution

Palau and Caroline Is (Chuuk).

SUBSPECIES

Nycticorax caledonicus caledonicus Scientific name definitions

Distribution

New Caledonia.

Hybridization

Hybrid Records and Media Contributed to eBird

  • Black-crowned x Nankeen Night Heron (hybrid) Nycticorax nycticorax x caledonicus

Distribution

Editor's Note: Additional distribution information for this taxon can be found in the 'Subspecies' article above. In the future we will develop a range-wide distribution article.

Habitat

Inland or coastal areas of fresh or brackish water, in areas permanently or semi-permanently flooded; normally in shallow water with forested margins, at swamps, lakes, pools, along slow-moving rivers , estuaries fringed with mangroves, inlets of sea. Also places with less or lower vegetation cover, including wet meadows, flooded grassland, reedbeds, saltmarshes, dunes, rock or coral reefs and atolls. Up to 1600 m in New Guinea (once 2200 m) (4); to 700 m in Melanesia (3). Also in built-up areas, e.g. urban wetlands, ornamental ponds in gardens; at such sites may roost and even breed (see Family Text).

Movement

Apparently essentially sedentary; post-breeding dispersal sometimes far-reaching, has presumably contributed to colonization of Sundas and Philippines. Also some movements connected with local water supply, e.g. in Darling–Murray basin in SE Australia (1). At least part of population at S of range seems to move N fairly regularly in winter and records from some Indonesian islands (e.g. Kai Is) perhaps only visitors from Australia during non-breeding season (6). Australian breeders may also be frequent visitors to New Guinea, with one ringed in Victoria recovered there; also vagrant to Tasmania, Lord Howe I (1), S Sumatra and Enggano I (7), Cocos Is (where has bred) (1) and Christmas I (Indian Ocean), as well as Vanuatu (3) and Taiwan (2003, 2008 and 2009) (8).

Diet and Foraging

Diet varied and adaptable. Great variety of fish (e.g. Gambusia, Carassius) (1), amphibians, crustaceans (shrimps and crayfish Cherax, Euastacus) (1), molluscs, crabs (Holthuisiana) (1), aquatic insects and their larvae (water beetles, crickets, water bugs, caterpillars, wasps, ants, dragonfly larvae and termites) (1); also eggs and chicks of other birds (especially colony-nesting species such as cormorants, ibis and spoonbills, but also starlings, ducks and House Sparrows Passer domesticus) (1), newly hatched sea turtles, mice (Mus) during plagues and human rubbish. Generally feeds alone, apparently maintaining territory, but will congregate when food is unusually abundant (1); uses passive techniques, especially Standing and Walking Slowly , but sometimes uses more active techniques, including Feet First Diving (1) and Swimming . Mainly crepuscular and nocturnal, but can be partially diurnal when feeding chicks.

Sounds and Vocal Behavior

Vocalizations generally considered to be similar to those of N. nycticorax, including a loud “wock” or “quok” in flight, a “rok” in threat (e.g. while foraging) and series of “wak-wak-wak-wak” notes on roost perch (2, 1).

Breeding

In Australia, timing depends largely on food availability related to rainfall and water conditions; can occur year-round, but mainly Oct–Mar (Dec–Jul on Great Barrier Reef to coincide with hatching of sea turtles) (1); recorded May and Aug–Dec on Borneo (9), Feb–Jun in Java, Feb–Jun, Aug and Nov in Philippines (2, 10), Sept–Nov in New Caledonia (11) and Nov in New Zealand (12). Highly gregarious, forming colonies of up to 250 pairs, or even 3000, but occasionally solitary; colonies are not synchronized (1); often with other herons, spoonbills (Platalea), cormorants (Phalacrocorax) and ibises (Threskiornis), but in such situations tends to remain apart from other species, sometimes with several nests on same tree (1). Nests in trees (including introduced pines and cypresses) (1) or large bushes, 20+ m above water; also under rock overhangs, on piles of coral rock and even on ground or in caves, on islands without trees where predation negligible; nest of sticks lined with leaves, typically 200–300 mm by 30–40 mm, but occasionally up to 350–500 mm by 80–150 mm, though some ground nests consist of just a few sticks, which may be stolen from other nests and are usually brought by male (1). Normally 2–3 pale green-blue eggs  (2–5), mean size 50 mm × 37 mm (1); incubation c. 3 weeks, by both sexes, commencing with first egg (1); chicks have dark brown down, white on belly, with cream-coloured bill edged black, orange-yellow to yellow eyes, white to orange-pink lores and olive-coloured legs and feet; fledging c. 6–7 weeks, but are fed away from the nest after 21 days (1). Normally single-brooded, but record of pair breeding in winter and then in summer. Sexual maturity usually in third year, but can successfully breed earlier (1).

Not globally threatened (Least Concern). In Australia, widespread and common in suitable habitat, some of which has suffered alteration due to drainage, clearing, burning, increasing salinity, groundwater extraction and flood control (1). Generally more numerous in N, E & SW Australia, and rare or absent in inland and NW Western Australia (1). Locally common in New Guinea and fairly common in Melanesia (3), but uncommon in Philippines (2), on Borneo (9) and most of Lesser Sundas (3). One colony in Sulawesi contained minimum of 70 birds, alongside ten N. nycticorax and some hybrids. Reportedly very rare on Java. Failed introduction to New Zealand in mid-19th century (1), but apparently colonized naturally, with nesting reported in late 1950s and again in 1995 (13, 12). Nominate of New Caledonia said to be quite common. Race crassirostris of Bonin Is, to S of Japan, became extinct around 1889 (see Family Text ).

Distribution of the Nankeen Night Heron - Range Map
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  • Migration
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Distribution of the Nankeen Night Heron

Recommended Citation

Martínez-Vilalta, A., A. Motis, and G. M. Kirwan (2021). Nankeen Night Heron (Nycticorax caledonicus), version 1.1. 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.runher1.01.1
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