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Little Spiderhunter Arachnothera longirostra Scientific name definitions

Robert Cheke, Clive Mann, and Guy M. Kirwan
Version: 1.0 — Published March 4, 2020
Text last updated December 30, 2018

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Field Identification

13·3–16 cm; male 10·3–16·1 g, female 8·8–13·7 g (race buettikoferi), male 12·5–15·8 g, female 9·3–14 g (cinereicollis). Male nominate race has very long, stout, gently decurved bill; plumage olive above, crown feathers dark-centred, sides of head grey, lores white, short blackish submoustachial streak; upperwing-coverts olive, remiges dusky brown with olive edges, tail dark brown, fringed olive and narrowly tipped whitish; throat and breast greyish white, breast tinged yellow, rest of underparts bright yellow, usually whiter on undertail-coverts, pectoral tufts orange; iris brown to dark brown; bill horn-brown, greyer on gonys and at base of mandible, or black above and pale grey below; legs black, blackish grey or bluish grey. Female is similar to male but smaller, has whiter throat, paler base to mandible, and lacks pectoral tufts. Juvenile is similar to female but browner, with bright olive-fringed wing feathers, and paler bill and feet. Race sordida is similar to nominate, but has dull whitish-grey lores, much shorter bill; pallida has much shorter bill than nominate, olive-green of upperparts paler and greyer, very white throat, underparts very pale yellow; <em>cinereicollis</em> is very long-billed, has bluish tinge to grey on sides of head, neck and throat, black at corner of mouth, with upperwing and tail greenish brown, breast to vent yellow, white undertail-coverts; zarhina has much longer bill than previous, but shorter wing, and much duller dorsal surface; niasensis also has longer bill and wings, and very pale yellow underparts; rothschildi is yellow below (like cinereicollis), but bill and often also wings shorter; atita differs from last in having longer bill, and yellow of underparts deeper, brighter and more golden; buettikoferi is browner and less olive than nominate, has paler pectoral tufts; and prillwitzi has brighter yellow underparts than nominate, and more orange pectoral tufts.

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.

Until recently considered conspecific with A. dilutior and A. flammifera, which see. Additional proposed races, all considered insufficiently distinct, are vantynei (from Jagalbed, Bombay, in W India), subsumed into nominate, and antelia (Trang, in S Thailand), heliocrita (Selitar, near Singapore), melanchima (upper R Siak, in E Sumatra), hypochra (North Pagai I), and exochra (South Pagai I), all synonymized with cinereicollis. Race cinereicollis originally spelt “cinireicollis” but this is a misspelt Latin word, and must be corrected. Ten subspecies recognized.

Subspecies


SUBSPECIES

Arachnothera longirostra longirostra Scientific name definitions

Distribution

SW, CE and NE India (Western Ghats from Goa region S to W Tamil Nadu and Kerala; E Odisha and N Eastern Ghats; Darjeeling; Arunachal Pradesh S to Meghalaya and Manipur), E Nepal, Bhutan, Bangladesh, Myanmar E to S China (W Yunnan) and W Thailand (S to Isthmus of Kra).

SUBSPECIES

Arachnothera longirostra sordida Scientific name definitions

Distribution

extreme S China (S and SE Yunnan, extreme NW Guangxi), NE Thailand and N Indochina.

SUBSPECIES

Arachnothera longirostra pallida Scientific name definitions

Distribution

SE Thailand and C and S Indochina.

SUBSPECIES

Arachnothera longirostra cinireicollis Scientific name definitions

Distribution

Malay Peninsula (S of Isthmus of Kra) S to Sumatra and satellite islands (except Banyak Is and Nias I).

SUBSPECIES

Arachnothera longirostra niasensis Scientific name definitions

Distribution

Nias I, off W Sumatra.

SUBSPECIES

Arachnothera longirostra prillwitzi Scientific name definitions

Distribution

Java (including Madura I) and Bali.

SUBSPECIES

Arachnothera longirostra buettikoferi Scientific name definitions

Distribution

Borneo.

SUBSPECIES

Arachnothera longirostra atita Scientific name definitions

Distribution

S Natuna Is.

SUBSPECIES

Arachnothera longirostra rothschildi Scientific name definitions

Distribution

N Natuna 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

Understorey of various types of forest, including mangroves, regenerating secondary forest, disturbed and heavily logged forests, forest edge, kerangas (Borneo), also coastal vegetation, secondary growth, plantations, gardens and cultivation, particularly around plantains (Musa) and gingers (Zingiberaceae), also rubber, cardamom, sholas (Aeschynomene sp.) and Albizia plantations. Generally below 600 m; up to 1500 m in S India, 75–305 m in Nepal, 2100 m in China, 1680 m in Peninsular Malaysia, and 2000 or 2200 m on Sumatra, Java and Bali; sea-level to 1500 m on Borneo.

Movement

Altitudinal movements recorded on Mt Mulu, in NW Borneo (Sarawak); movements of up to 6 km recorded in Peninsular Malaysia. Thought to undertake local movements in Nilgiri Hills, in SW India. Nomadic in some areas.

Diet and Foraging

Nectar , insects, and spiders (Araneae). Known foodplants include Canna sp., Erythrina, mistletoes (Loranthaceae), Melastoma spp., Musa sp., Spathodea sp. and unidentified Zingiberaceae. Forages singly and in pairs, mostly in lower levels of vegetation. Takes insects from spider webs, and from pools of water in vegetation. Nectar-robbery recorded. Pollinates and takes nectar from durian trees (Durio); pollinates Strelitzia nicolai, also Musa species with either erect or pendulous inflorescences.

Sounds and Vocal Behavior

Much geographical variation. Songs include “which-which”, twice per second for c. 2 minutes, continuous “tee-chu”, first note rising, second falling, and squeaky “chew-chew-chew-chew” whistle; in S India described as continuous, syncopated, strident, metallic “clínk-clínk-clínk”, each note an upstroke, and in NE India as simple, metronomic, metallic upstroke “clínk-clínk…”, recalling Common Tailorbird (Orthotomus sutorius), or more varied “wink-link-wink-wink-link-link-wink”, irregular and with more noticeable pitch differences; in Malay Peninsula “tee tay” and “ti tee-tee-tah”, stressed on first syllable. Antiphonal singing occurs, presumably by pair-members. In flight, sharp “weechoo” or “cheek-cheek-cheek”; high-pitched “tik-ti-ti-ti”, first note higher, repeated continuously; harsh metallic “cheet” or “chee-chee”; repeated “chee-chee-chee” or “chip-chee-chee” or “chip-chip”; loud, harsh “sheep” repeated up to 25 times; loud “jit-jit”, increasing in rate and intensity.

Breeding

Laying in India in Dec–Aug (chiefly Jan–May) in SW and Jan–Nov (chiefly May–Aug) in Assam; probably Mar–Sept in Nepal, Jan in Thailand, egg-laying calculated as Dec–May (once early Oct), nestbuilding observed mid Aug, nestlings found in Apr and Oct, and juveniles in all months (most in May–Jun, fewest Sept–Dec) in Malay Peninsula, May–Jun and probably Aug on Sumatra, in all months except Nov on Java; on Borneo, oviduct eggs/active gonads in Jan, Mar–Apr, Jul and Sept–Dec, food-carrying adults (Sabah) in May and Nov and juveniles in Jul–Aug. Nest a compact cup 10 cm deep, with semi-circular entrance hole on one side (some nests have two entrances), constructed from leaf skeletons, soft grass and vegetable down neatly felted together, lined with fine grass, and attached by rim to underside of banana leaf by cobwebs or vegetable cotton passed through leaf and knotted on upper surface, or made from rootlets, dead leaves, plant fibres and cobwebs in tunnel created by the sewing-up of ginger and plantain leaves; sometimes placed under Khydia leaf, or in elephant grass, or under giant creeper or large dock (Rumex) leaf or on castor-oil plant (Ricinus communis); can be as little as 0·5–2·5 m above ground; nest described also as trough-like, closed at one end to form cup, with entrance tunnel pointing downwards. Clutch two or three eggs, dull white or creamy with zone of heavy red-brown or purple-brown spotting, or with very few spots, or unglossed pinkish white to salmon-pink with sparse reddish speckles all over and sharply defined ring of red-brown spots around broad end, size 16·3–19·1 mm × 12·3–13·9 mm (India), 17·1–17·5 mm × 12·8–13·4 mm (Peninsular Malaysia), 16·2–20·2 mm × 12·4–14·7 mm (Java); no information on incubation and nestling periods. Nests parasitized by Violet Cuckoo (Chrysococcyx xanthorhynchus), Asian Emerald Cuckoo (Chrysococcyx maculatus), Common Cuckoo (Cuculus canorus), Large Hawk-cuckoo (Hierococcyx sparverioides) and Malay Hawk-cuckoo (H. fugax), based mainly on data from India and Thailand. Oldest recorded bird five years old.

Not globally threatened (Least Concern). Locally common in India in Western Ghats and NE; very scarce and local in SE Nepal, where recorded also in C; uncommon in Bhutan; locally common in Bangladesh; common in Tenasserim, but rare elsewhere in Myanmar, generally common in Thailand except E, locally common in S Laos, and common in Peninsular Malaysia; not uncommon on Sumatra, where density of up to c. 165 birds/km² in Harapan Rainforest Ecosystem Restoration Concession; common on Borneo. Occurs in numerous protected areas, examples of which are Nonggang National Nature Reserve, in SE China, Kaeng Krachan National Park and Khao Pra Bang Wildlife Sanctuary, in Thailand , Cat Tien National Park, in Vietnam, Way Kambas National Park, on Sumatra, Gunung Gede-Pangrango National Park, on Java and Bali, and Danum Valley Conservation Area and Tanjung Puting National Park, on Borneo.

Distribution of the Little Spiderhunter - Range Map
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  • Year-round
  • Migration
  • Breeding
  • Non-Breeding
Distribution of the Little Spiderhunter

Recommended Citation

Cheke, R., C. Mann, and G. M. Kirwan (2020). Little Spiderhunter (Arachnothera longirostra), 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.litspi1.01
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