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White-throated Needletail Hirundapus caudacutus Scientific name definitions

Philip Chantler and Guy M. Kirwan
Version: 1.0 — Published March 4, 2020

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Introduction

The White-throated Needletail is a large swift with a short square tail and weak, short rectrix spines, a long body and long broad wings, the latter with blue gloss fading to green on remiges and coverts, an off-white mantle, contrastingly white throat, forehead and ‘horseshoe’ mark on the flanks and undertail-coverts on an otherwise brown body. It is a long-distance migrant, the nominate race nesting in the temperate and boreal forest zone between central Siberia and Japan, with a second population (race nudipes) in the Himalayas, and wintering mainly in southern New Guinea and eastern Australia, although those breeding in the Indian subcontinent perhaps spend the non-breeding season further north and west. Unsurprisingly, given such migrations and its powerful flight, vagrants have wandered as far afield as western Europe, the Aleutian Islands (Alaska), subantarctic Macquarie Island (Australia) and the Seychelles. Like most swifts, White-throated Needletail spends most of its life airborne, but the birds nest (and roost) in holes trees, including those previously excavated by woodpeckers (Picidae), and in Japan at least perhaps also breeds on cliffs.

Field Identification

Graceful and powerful flight, with slow purposeful turns, much gliding and soaring, and capable of sustained high-speed flight on surprisingly shallow wingbeats, but also broad circling flight at great heights (1). Large swift with short square tail and weak, short rectrix spines  protruding up to 6 mm beyond web; long full body and long broad wings  ; dark wings with blue gloss fading to green on remiges and coverts; off-white mantle , contrastingly white throat , white forehead  , and white horseshoe mark on flanks and undertail-coverts  on otherwise brown body.

Similar Species

Distinguished from other needletails by highly constrasting white throat patch. Silver-backed Needletail (Hirundapus cochinchinensis) has much less clear-cut and duller patch, and lacks pale forehead, while pale saddle on mantle is usually paler than in Brown-backed Needletail (H. giganteus) and Purple Needletail (H. celebensis), from which two species it also differs in having squarer-cut tail (2).

Plumages

Juvenile

Rather variably plumaged, and some are very close in morphology to adult. Overall less glossy, especially on upperwing and tail, with darker and less contrasting throat, usually a less obvious mantle patch, less green gloss on upperparts and wings, black tips to undertail-coverts (the most consistent difference), black streaking and spotting on lower flanks, and usually has dusky or gray-brown forehead and lores. Prior to post-juvenile molt (on winter quarters), some paler gray feather bases (white on nape and rump) to the body can be visible, giving a mottled effect (2).

First-year

More similar to adult following post-juvenile molt, but typically retains gray-brown forehead, has black-fringed tip to shortest tertial, still has some black fringes to undertail-coverts, and very worn (retained) remiges and larger wing-coverts (2).

Adult

Has broad white and highly contrasting throat patch, from gape, along lower ear-coverts, and onto lower throat, and white band on lores (where broadest) and forehead (where sometimes browner). Rest of head and nape dark olive-brown, glossed greenish blue in fresh plumage, but with pale brown feather bases visible when worn, although white feather bases are rarely seen, even when heavily worn. Darkest parts of head are those tracts adjacent to the white throat patch. Saddle pale brown, palest on centre of lower mantle and back (especially when worn), but progressively darker towards nape. Scapulars olive-brown and central rump, clearly darker at sides and on uppertail-coverts. Tail black, glossed green, with rectrix spines projecting up to 6 mm on central feathers, or 2.5 mm on outermost feathers. Remiges black, paler brown on inner webs of primaries, but not to their tips; wing-coverts black. Primary-coverts and remiges glossed blue, and other coverts glossed on outer webs and tips to inner webs, while the rest of the inner webs are glossed green, but gloss usually hard to see in the field, and is lost with wear. Inner webs to tertials white. On underwing, remiges paler, and fairly uniform with greater primary-coverts and greater coverts. Median and lesser coverts, however, are darker, black-brown, uniform with the axillaries. Breast and upper flanks to vent dark olive-brown, with brown gloss when fresh. Lower flanks and undertail-coverts white, forming highly contrasting and distinctive horseshoe mark. Sexes alike.

Molts

Few published data.

Measurements

Linear Measurements

Overall length 19–21 cm.

Linear measurements (in mm, with sample sizes and means in parentheses where available, from 2):

Wing length Tail length (including spines)
Adult male 200–213 (n = 7, 208) 47–53 (n = 11, 49.7)
Adult female 198–211 (n = 10, 206) 47–51 (n = 7, 48.8)
Juvenile male 203–215 (n = 9, 209) 47–55 (n = 9, 50.3)
Juvenile female 195–215 (n​​​​​​​ = 10, 206) 48–53 (n = 10, 50.6)

Mass

Male 47.4–169 g, female 64.5–125.0 g (3, 4, 5).

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 Hirundapus cochinchinensis, with which was in the past sometimes considered conspecific (6). Taxon formosanus formerly placed in present species (6), but has been shown to be virtually identical to nominate race of H. cochinchinensis, to which it clearly belongs (see that species).

Geographic Variation

Variation is expressed in color of the lores, and upperparts, and perhaps also in behavior, with some populations potentially more, or wholly, sedentary, versus long-distance migrants.

Subspecies

Two subspecies recognized.

H. c. caudacutus (Latham, 1801)—breeds from central Siberia east to Sakhalin and the Kuril Islands, and south to northern and eastern Mongolia, northeast China, Korea, and Japan; winters in southern New Guinea and eastern Australia. Proposed race bourreti (from Laos, where a presumed passage migrant) is indistinguishable from nominate (7).

H. c. nudipes (Hodgson, 1837)—breeds in the Himalayan foothills, irregularly from northern Pakistan east to Assam, Arunachal Pradesh through northern Myanmar to southern China (Sichuan south to Yunnan); wintering area not well documented, possibly includes Malay Peninsula and Java. Differs from nominate caudacutus apparently in migratory habits, and has black forehead and lores, less distinct (browner and less silvery-gray) (2) mantle patch, generally darker underparts (with green gloss) and underwing-coverts (2), while upperparts are glossed darker blue (2), suggesting considerable distinctiveness. Also averages marginally shorter-winged (194–214 mm, versus 198–213 mm in nominate (8), and rectrix spines protrude up to 5 mm, versus 6 mm in nominate (2). Specimens in NHMUK from China, however, appear intermediate, having white lores and blue-glossed upperparts (9).


EBIRD GROUP (MONOTYPIC)

White-throated Needletail (White-lored) Hirundapus caudacutus caudacutus Scientific name definitions

Systematics History

Hirundo caudacuta Latham, 1801, Index Ornithologicus, Supplement II, p. lvii.—New Holland [= New South Wales, apud Mathews 1918].

Type not known to be in existence.

Synonyms:
Hirundapus caudacutus caudacutus var. uchidai Ishizawa, 1928, Annotationes Ornithologiae Orientalis 1:146, pl. 4, fig. 1.—Nikko, Province of Simotsuke, Hondo [= Namma-mura district, Kamitsuga-gun, Tochigi Prefecture, Honshu], Japan (10, 11). Based on an adult (female?) collected on 24 October 1925 by T. Ishizawa (12), held at the Forest and Forest Products Research Institute, Tsukuba, Japan (FFPRI 1498) (10, 11). Described as a color variant at infrasubspecific level, which as a result means that the name has no standing (having not been adopted as valid by any subsequent author) and cannot have a type (11).
Chaetura caudacuta bourreti David-Beaulieu, 1944, Les Oiseaux du Tranninh, p. 89.—Xieng Khouang [19°20’N, 103°30’E], northern Laos. The holotype is a female collected by M. David-Beaulieu on 24 April 1940, and now held at the Chulalongkorn University, Bangkok (7); the latter author discussed reasons for considering this name a synonym of the nominate.

Distribution

Breeds from central Siberia east to Sakhalin and Kuril Islands, and to northern and eastern Mongolia, northeast China, Korea, and Japan; winters in southern New Guinea and eastern Australia.

Identification Summary

Described under Plumages.


EBIRD GROUP (MONOTYPIC)

White-throated Needletail (Himalayan) Hirundapus caudacutus nudipes Scientific name definitions

Systematics History

Cypselus (Chaetura) nudipes Hodgson, 1837, Journal of the Asiatic Society of Bengal 5:779.—Nepal.

Four syntypes, all presented by Brian Houghton Hodgson, are held at the Natural History Museum, Tring, of which one, a relaxed mount, is NHMUK 1843.1.13.173 (13, 14).

Distribution

Himalayan foothills, irregularly from northern Pakistan east to Assam, Arunachal Pradesh through northern Myanmar to southern China (Sichuan south to Yunnan); wintering area not well documented, possibly includes the Thai-Malay Peninsula and Java, but there are recent sightings of quite large numbers of individuals positively identified as this subspecies in the Mekongga Mountains, southeast Sulawesi (15).

Identification Summary

Differs from nominate caudacutus apparently in migratory habits, and has black forehead and lores, less distinct (browner and less silvery-gray) mantle patch (2), generally darker underparts (with green gloss) and underwing-coverts (2), whilst the upperparts are glossed darker blue (2), suggesting considerable distinctiveness. Also averages marginally shorter winged (194–214 mm, versus 198–213 mm in the nominate (8), and rectrix spines protrude up to 5 mm, versus 6 mm in nominate (2). Specimens in NHMUK from China, however, appear intermediate, having white lores and blue-glossed upperparts (9).

Distribution

In north, breeds from the Vasyuagan River, in central Siberia, across the Russian Far East, including Sakhalin Island, to northern Japan (Hokkaido south to central Honshu) and south to Mongolia, northeast China and the Korean Peninsula; this population winters in southern New Guinea and Australia, principally across the eastern half. A southern population (recognized at subspecies level) is either resident or partially so in the Himalayas, from northern Pakistan east through Nepal, Sikkim and Bhutan to Arunachal Pradesh (India), western Yunnan and southern Sichuan (China); at least some migrate southeast in winter, to Thailand and Indochina, but also as far afield as West Java, but at present (due to the lack of specimens and difficulty in making subspecific identifications in the field) it is unclear whether the majority of records in South-East Asia pertain to Himalayan or Siberian migrants, and consequently whether the latter population may winter over a much larger area than currently believed.

Habitat

In north of range, wooded lowlands and sparsely vegetated hills. In Himalayas at 1,250–4,000 m, feeding over river valleys and upland meadows and pastures, as well as subtropical, broadleaved and temperate forest between 6,00 and 3,200 m in Bhutan, with occasional records to 400 m and 3,500 m (16). Winters in both coastal and mountainous areas, apparently using tree hollows for roosting (17). In Snowy Mts, Australia, abundant winterer above 1,800 m, and common at 1,530–1,800 m. In Wallacea recorded from sea level to 800 m on Sangihe, 900 m on Peleng (Banggai Islands) (18), 500 m on Buru and 3,000 m on Lombok, these mountains being free of snow. Recorded in small numbers over woodland in Brisbane Forest Park, Australia. In lowland rainforest zone of Papua New Guinea recorded over forest edge and non-forest.

Movement

Nominate race is a long-distance migrant. Himalayan race nudipes may be resident or perhaps just summer visitor, e.g. in Bhutan, where extreme dates are February–October (mainly late March–September) (19,20,16) and also said to vacate breeding areas in Nepal (21); reported to appear and disappear at localities rather suddenly, making clear assessment of migratory status complicated; local and uncommon passage migrant between September and December in Thailand, where perhaps also winters (22), records in South Annam, Vietnam, in March–April (23), and two specimens from Bokor, Cambodia, December 1927 (24). Two specimens of nudipes also available from West Java, November 1922 (5,25) and at least some Peninsular Malaysian (26) and Bornean records may also pertain to this taxon (27). Nominate race is present on Siberian breeding grounds mid May to late September, around Lake Baikal from second half of May to late August, but in Russian Far East sometimes even present until late October (3); summer visitor, Japan, mainly April–September, with records until November (28,29); migrates through China, Indochina, and to lesser extent southern and eastern Thailand (September–November and February–April) (22), Wallacea and New Guinea, but is little more than a vagrant (November, March–May) in Peninsular Malaysia (26); recorded on passage and possibly as winter visitor through Wallacea (30): mid October, Sangihe (31); October to early April, Sulawesi (32); October, Taliabu (Sula Islands) (33,18); March–April, Peleng (Banggai Islands) (34); November and February, Buru (35); late April, Halmahera (36); January and early April, Lombok (32); late September, October and January, Flores; December, Lembata (37); October, Timor (32); December, Timor-Leste (38); recorded from Aru Islands in early April (39); however, just three records in Philippines (in April, September and October) (40). Migrates through South-East Asia September–November (occasionally from late Aug) (41) and winters in Australia (including Tasmania) December–March (42), with smaller numbers in southern New Guinea, mainly in southern lowlands and Southeast Peninsula (43,2,44) (also January–February records from Lihir in New Ireland) (45); many records of overshooting birds in New Zealand, mainly November–April, with some reaching as far as the Snares Islands and Chatham Islands (46,47,48,49). Among observations in all months between May and August in Australia, as far south as Victoria and New South Wales (5), the species has been recorded from the Cape York Peninsula, Queensland, with Pacific Swift Apus pacificus in July (50), and the Snowy Mts, New South Wales, in austral summer (51), presumably non-breeding birds. In spring, recently recorded for first time on Hainan, April (52); migrates through Hong Kong mid March to early May (2), South-East Asia as late as May, and northeast China in May. Vagrant to Aleutian Islands (four records, all in May, 1974, 1978, 1984 and 1985, with the only specimen unsurprisingly being of the nominate race) (53,54), Seychelles (twice) and Rodrigues (55,56), Christmas Island (57), Cocos-Keeling Islands (58), Fiji (2), New Caledonia (59) and even subantarctic Macquarie Island (Australia) (5) and the Campbell Islands (New Zealand (60), as well as western and northern Europe (Denmark (61), Finland, Netherlands (62), Norway, Sweden), with British and Irish records April–July and November; also single November records from Malta and Spain (63).

Diet and Foraging

Coleoptera, Hemiptera and Hymenoptera recorded for race nudipes (64). In Siberia, nominate race, perhaps mainly Coleoptera, among a range of insects reported as debris in nests (3). Wintering birds  in New South Wales, Australia  , recorded feeding on Pheidole flying ants (65); elsewhere in Australia, diet includes Coleoptera, Hemiptera, Diptera, Hymenoptera, Isoptera, Lepidoptera and Orthoptera (5). Gregarious, forming both large single-species flocks  (sometimes numbering thousands on winter quarters (5) and regularly consorting with other Hirundapus or Pacific Swift Apus pacificus on migration (2), but rarely associates with other species while foraging during breeding season; occasionally observed feeding with Fairy Martin Petrochelidon ariel during non-breeding season in Australia (5). Forages at all heights, from just 1 m above ground to at least 1,800 m above it, occasionally observed skimming ground taking insects on mud; in Australia, observed occasionally taking insects on tree trunks or even briefly clinging to flowers searching for prey (5).

Sounds and Vocal Behavior

Typically, a rapid, insect-like chattering or twittering (softer than Apus screams), e.g., trp-trp-trp-trp-trp-trp..., of varying duration and speed, but can be loud and audible over reasonable distances; but also reported to give a loud, sharp cry; a chirp; a piping sound, likened to a sandpiper (Scolopacidae); a churring twitter; and, when handled, a querulous note, and a repeated cheep from an injured individual (5,2). On wintering grounds, said to be less vocal than Pacific Swift Apus pacificus (5).

Breeding

Gravid female nudipes collected in mid April in northern Cachar, north India (64); nominate race lays late May to early June in Siberia and Japan (66,28), but young in nest recorded as late as August in Russia (67). Breeds Ussuriland late May to early June; eggs laid from mid June and fledglings leave nest late July to early August (67). Nest consists of scrape, 35–50 cm in diameter, in debris at bottom of tree hollow, e.g. larches (Larix) and oaks (Quercus) (3), but also reported nesting in cliffs in Japan (17); two pairs apparently recorded prospecting old woodpecker hole in an Acer tree in Pakistan (68). Clutch 2–7 white eggs, mean size 32·2 mm × 22·3 mm, mass 7.9–8.9 g (67); incubation commences with first egg, both sexes incubating, period 40 days; chicks blind and naked on hatching; fledging period 40–42 days.

Not globally threatened (Least Concern). Race nudipes local and uncommon throughout most of range, though fairly common in Bhutan. Nominate race becomes commoner farther east within Siberian range. Local declines reported in Japan in response to tree removal (69). A significant decline during 1951–2010 has been detected in the population wintering at Victoria, Australia, which has been attributed to the accelerated destruction of the Siberian forests, where the birds need old trees with hollows in which to breed (70). Abundant in some areas of Australian winter quarters where flocks involving tens of thousands, once 50,000–100,000, have been reported (5), with smaller numbers in southern New Guinea (2). Possible that species occasionally winters as far north and west as Thailand (2). On the other hand, recent (April 1995) first record from Myanmar (71) has been speculated to perhaps indicate that Himalayan breeding population reaches farther southeast than thought (2), but see also Movement Ecology.

Distribution of the White-throated Needletail - Range Map
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Distribution of the White-throated Needletail

Recommended Citation

Chantler, P. and G. M. Kirwan (2020). White-throated Needletail (Hirundapus caudacutus), 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.whtnee.01
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