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Gray-rumped Treeswift Hemiprocne longipennis Scientific name definitions

David Wells and Guy M. Kirwan
Version: 1.0 — Published March 4, 2020
Text last updated February 17, 2014

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Field Identification

21–25 cm; 42·8 g (one harterti). Dark forehead-crest. Male has ear-coverts rufous, rest of face black, with no white striping; greenish grey from lower mantle towards rump, rump pale grey, rest of upperparts glossy blue- to green-shot black; underwing-coverts black with glossy green fringing; underparts uniformly pale greenish-grey, with belly and undertail-coverts contrastingly whitish. Averages larger than H. coronata but shorter-tailed, streamers not projecting past folded wingtips, and has less rufous on face, while also note more contrast in both upperparts (with rump) and underparts (1). Widely sympatric H. comata obviously darker and smaller than present species, and also has white facial stripes and bronzy upperparts (1). Female as male, but with ear-coverts deep bottle-green. Juvenile has head and body more or less as in H. coronata, but dorsal patterning often more complex, particularly on cap, which lacks contrasting lateral band, and has no obvious pale loral spot; first-winter has adult-type body feathers, but retained juvenile wing and tail feathers (1). Races harterti and perlonga shade darker than nominate on anterior underparts (some overlap between harterti and nominate in this feature) (1), and rump less pale in relatively large perlonga (wing of male 175–178 mm, vs. 154–169 mm in harterti) (1); <em>wallacii</em> largest (wing of male 179–183 mm, vs. male of nominate 167–168 mm) (1), with plumage much as nominate.

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 H. coronata, with which formerly sometimes treated as conspecific. Several races have been described, but most nowadays considered invalid; ocyptera (Nias I) and thoa (Batu Is, Pagai Is, Enggano I) synonymized with perlonga, anochra (Natuna Is) with harterti, and dehaani and mendeni (from archipelagos E of Sulawesi) with wallacii. Four subspecies recognized.

Subspecies


SUBSPECIES

Hemiprocne longipennis harterti Scientific name definitions

Distribution

S Myanmar (S Tenasserim) and SW Thailand S and E to Sumatra, Borneo and intervening islands, and Sulu Archipelago (E to Tawitawi).

SUBSPECIES

Hemiprocne longipennis perlonga Scientific name definitions

Distribution

W Sumatran islands from Simeulue S to Enggano.

SUBSPECIES

Hemiprocne longipennis longipennis Scientific name definitions

Distribution

Sunda Strait (Panaitan I) through Java to Lombok, and Kangean Is (E Java Sea).

SUBSPECIES

Hemiprocne longipennis wallacii Scientific name definitions

Distribution

Sulawesi, including S and E satellites, and Sula Is.

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

Groves of large trees and edge and canopy breaks of more continuous semi-evergreen and evergreen forest inland, locally tall mangroves and coastal casuarinas, also making use of tall plantation (e.g. mature rubber) (2) and mature parkland trees. Everywhere selects well-exposed, bare perches at outer edge of the high canopy. From plains level to 1200 m in Malay Peninsula, to 1400 m on Sulawesi (1), 1500 m on Borneo (3) and 1550 m in Java.

Movement

Breeds over its whole altitudinal range, with probably no more than post-breeding local dispersive movements; vagrants or rare residents recorded in Philippines on Sibutu (Nov 1971) and Tawitawi (Aug 1994) (4).

Diet and Foraging

Flying arthropods; prey selection hardly known, but regularly attends swarms of alate termites and, in Borneo, recorded taking bees from the edge of a flying swarm. Prey caught during long (300–400 m) (2) sorties out from a favoured tree crown , typically well clear of vegetation surfaces. Regularly uses same perches year after year (2). In Selangor, Malaysia, mean foraging height above open ground was 35 m, and above forest canopy was 47 m. Like other Apodiformes, drinks by scooping water in a fast, skimming swoop down to an open surface. Especially active at dusk and immediately following rain (2), when sometimes consorts with other aerial feeders, and forms flocks of its own species of up to 70 (5).

Sounds and Vocal Behavior

Gives shrill wader- or tern-like calls both on perch and in flight (sometimes most excitedly, even hysterical-sounding, when coming into land), with considerable variation reported, the commonest being a harsh, piercing “ki”, sometimes given in series, “ki-ki-ki-kew”; gives disyllabic “too-eit” or “whit-kep”, the second note sounding slightly higher and metallic, somewhat like H. coronata (1).

Breeding

In N Hemisphere, laying season overall Feb–Aug/Sept (chick records in Oct in Peninsular Malaysia) (1), peaking in Mar–Jun, but also eggs in mid-Dec on Borneo (1); in S (Java and Sulawesi) (1) active nests Dec–Aug. Double-brooded in Kalimantan Barat (Borneo), Apr–May and Aug–Sept (3). Nesting dispersed but, as with H. coronata, often with several other pairs in the neighbourhood. Copulates on perch (6). Nest as that of H. coronata, built by both sexes, typically a half-saucer of hardened saliva incorporating small scraps of moss, bark flakes and body feathers, c. 36 × 24 mm, maximum outside depth 12 mm, built out as a bracket 5–30 m up on a thin, exposed branch. Lays one white egg, size 25·6 mm × 17·4 mm (2); both pair-members incubate and both tend the chick; incubation and fledging periods not precisely recorded, but is at least 50 days (2); chick down is grey.

Not globally threatened (Least Concern). More or less common through most of its range, and under no serious threat overall. As with H. coronata, preference for patchy tree cover and edge habitat over continuous natural forest suggests that it may in fact have benefited from some forest disturbance; the species is absent, however, from still rapidly expanding oil palm agriculture, and populations in the plantation landscape would benefit from a commitment to the maintaining of natural or semi-natural shelterbelts. The opposite trend is set in Malaysia, where over-use of organophosphate pesticide sprays in suburban parkland habitat is another rising issue. Pesticides are suspected to be behind a recent population decline in Singapore. Elsewhere, the general impression is that bird-hunting, exacerbated by expanding availability of airguns, will have damaged non-forest populations through much of W Indonesia; hunting has caused quite severe reduction of nominate race, along with nearly all bird species, in lowland Java.

Distribution of the Gray-rumped Treeswift - Range Map
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Distribution of the Gray-rumped Treeswift

Recommended Citation

Wells, D. and G. M. Kirwan (2020). Gray-rumped Treeswift (Hemiprocne longipennis), 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.gyrtre1.01
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