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Black-rumped Buttonquail Turnix nanus Scientific name definitions

Josep del Hoyo, Nigel Collar, and Guy M. Kirwan
Version: 1.0 — Published March 4, 2020
Text last updated June 28, 2015

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Field Identification

14–16 cm; male 40–46 g, female 57·5–62·4 g (1); female larger. Small, rather dark Turnix with slender bill and orange-rufous face and breast; prominent barring on sides of breast and spotting on flanks; pale yellow eyes. Female has very slightly brighter red underparts. Individually variable (1) but has pale blue to whitish eyes, darker upperparts, richer rufous breast with less extensive black markings on sides compared to formerly conspecific T. hottentotus (see also Taxonomy); male much duller and more heavily marked than female. Differs from widely sympatric T. sylvaticus in barred breast and flanks, darker upperparts with no contrast in upperwing, lack of central coronal stripe, and rufous face in female (1).

Systematics History

Often considered conspecific with T. hottentottus, but treated as separate species in a recent systematic list (2) and differs on account of female underparts unspotted vs black-spotted and/or black-barred on tan breast and white flanks (3); male underparts pure white below tan breast vs broadly barred from breast to mid-belly and thence onto flanks (3); rump and uppertail (both sexes) blackish vs as rest of upperparts or slightly darker (2); irides bluish-white vs pale yellow (ns[2]); legs whitish-flesh vs yellow (ns[2]); clear supercilium vs white-flecked (ns[1]); slightly smaller size (3) (assume 1); grassland vs “restionaceous fynbos” (3) (1); and apparent differences in migratory behaviour, but these not clearly understood (ns). Possible N races lucianus and insolatus now considered inseparable from nanus. Monotypic.

Subspecies

Monotypic.

Distribution

Irregular and local in sub-Saharan Africa, mainly from Nigeria E to Uganda and Kenya, S to Angola and E South Africa; status and limits of range particularly uncertain in W Africa (reported W as far as Sierra Leone and as a breeder to Ivory Coast) (4).

Habitat

Short (characteristically 25–50 cm tall) (1) and fairly open grassland and savanna including dry sandy plains (1), often in moist zones including floodplains (5) (though usually little standing water) (1); also found in fallow fields, native gardens, scrubland, areas of short herbage, and edges of thickets; occurs from sea-level up to 1800 m. Possibly tracks fire cycles in places, and evidently leaves some areas when vegetation becomes too tall and dense (1); typically occurs in shorter grassland than T. sylvaticus (6). Breeds in wet grassland and probably rice fields, away from trees, plains occasionally in somewhat marshy, harvested fields of sugarcane.

Movement

Poorly understood. Resident and local intra-African migrant; apparently itinerant over most of range, where tends to be breeding migrant during rains. Resident in Kenya, perhaps Uganda (recorded only Apr–Oct) (7) and South Africa; breeding visitor to Malawi (records Apr–Dec) (6), Zimbabwe (in wet season) (8) and perhaps Zambia (although situation in latter country complex, and may only move locally in response to burning or flooding, with dry-season influx from Kalahari Basin reported) (1); probably only vagrant to Nigeria, although breeding recorded; erratic appearances in Cameroon. Migrates at night. Sometimes flushes twice, but is generally very difficult to flush, flying only short distance before returning to cover, and usually preferring to run from perceived danger (1) (even dogs) (9).

Diet and Foraging

Few specific data available. Seeds of grasses and weeds; invertebrates including insects and their larvae. Food taken on ground. Usually recorded singly or in pairs, only occasionally in small groups (1).

Sounds and Vocal Behavior

Vocalizations offer best means of detection and provide extremely strong evidence of breeding, but singing season can be very brief, perhaps just a few weeks in some areas (e.g. in Congo-Brazzaville). Female advertising call is similar to, but considered shorter and faster than, T. sylvaticus, a low “hoom hoom hoom” uttered at rate of 1·6 notes/second, with virtually no pause between notes; sometimes a flufftail (Sarothrura)-like “oooooop-oooooop”; also reported to give a low- and even-pitched humming noise that last c. 1 minute or more (1).

Breeding

Laying occurs in most months, but locally during or at end of rainy seasons (e.g. Sept–Feb, mainly Dec–Jan, in Zimbabwe) (1); elsewhere, in Jul (9), and Oct–Feb in Zambia (5), Sept and Dec–Jan in KwaZulu-Natal (8), with chicks in Jan in Uganda (7). Solitary breeder; females possibly polyandrous. Nest is shallow scrape (50–75 mm wide and 20 mm deep) (9), lined with grass, under or between grass tussocks with standing stems bent to form loose canopy, or under sheaf of fallen grass without canopy. Usually three greenish-white (9) eggs with dark grey or olive-brown markings (9) (2–6), 20·5–24·5 mm × 17–20 mm (9); incubation 12–14 days by male alone; downy young undescribed. No further information.

Not globally threatened (Least Concern). Uncommon or locally common, but cryptic in plumage and behaviour and easily overlooked or misidentified (6); less numerous than partially sympatric T. sylvaticus. Locally common in Congo, Uganda (where precise status unclear) (7) and Kenya (though few records in latter country since 1950) (1); widespread but local in Zambia (where estimate of c. 40,000 individuals in Liuwa Plain National Park) (1) and Malawi (although very few recent records in latter) (6); uncommon and local in Mozambique and Zimbabwe, and apparently also in W Africa, where some records may be doubtful (10). Occurrence in Ghana, which long rested on a single specimen collected during dry season, recently reconfirmed by records since 2005 in N & SE of country, in Jul–Oct (wet season) and the species’ range there could be quite extensive (11). Occurrence in Botswana unconfirmed (1) and just two records in Tanzania (12). Very rare in South Africa, where range has undergone major contraction, probably due, at least in part, to overgrazing, human settlement (1), trampling and excessive burning of habitat, but remains regular around Morgan Bay. Association with dry and heavily grazed grasslands (including rice cultivation), and attraction to areas disturbed by cattle, suggest that species is likely to be secure; however, overgrazing could be a threat in some areas and the species is probably dependent on wet areas for breeding.

Distribution of the Hottentot Buttonquail (Black-rumped) - Range Map
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  • Year-round
  • Migration
  • Breeding
  • Non-Breeding
Distribution of the Hottentot Buttonquail (Black-rumped)

Recommended Citation

del Hoyo, J., N. Collar, and G. M. Kirwan (2020). Black-rumped Buttonquail (Turnix nanus), 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.hotbut3.01
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