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Cape Robin-Chat Cossypha caffra Scientific name definitions

Nigel Collar
Version: 1.0 — Published March 4, 2020
Text last updated October 1, 2018

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Field Identification

16–17 cm; 25–34 g. Nominate race is olive-grey from crown to lower back, darker wings (with white post-carpal edge), chestnut rump and tail, latter with grey-brown central feathers; broad white superci­lium, blackish mask; white narrow moustachial line bordering orange-white chin with dark whisker mark, shading to orange-buff breast, grey breast side and flanks , whitish belly and orange-buff vent and undertail-coverts; bill and legs brownish to blackish. Sexes similar. Juvenile is spotted buff above, scaled dusky below. Race nama­quensis is like nominate but larger, with stronger supercilium; <em>iolaemus</em> is darker above and below than nominate; kivuensis similar to previous but more richly coloured below.

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.

Proposed races vespera (E Zimbabwe), ardens (Transvaal) and drakensbergi (NE South Africa) synonymized with nominate. Four subspecies recognized.

Subspecies


SUBSPECIES

Cossypha caffra iolaema Scientific name definitions

Distribution

S South Sudan and N Uganda S to Malawi and N Mozambique.

SUBSPECIES

Cossypha caffra kivuensis Scientific name definitions

Distribution

SW Uganda, E DRCongo, W Rwanda and NW Tanzania (Ngara).

SUBSPECIES

Cossypha caffra namaquensis Scientific name definitions

Distribution

S Namibia and W and C South Africa (Northern Cape E to Free State).

SUBSPECIES

Cossypha caffra caffra Scientific name definitions

Distribution

E Zimbabwe and N, E & S South Africa (S to Western Cape), including Swaziland and Lesotho.

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

Edges of montane forest, typically bracken-briar and similar ecotonal vegetation adjacent to forest patches, with little penetration of forest interior; also highland tea and coffee plantations, woodland, gardens, giant heath, edges of bamboo and forested ravines. S of R Limpopo more generalized, found in any habitat with dense stands over 2 m in height, and including low-lying woodland, bushveld, fynbos, exotic plantations, willow belts, large gardens and parks; in dry SW areas, largely confined to riparian vegetation and vicinity of human settlements. Occurs at 1500–3400 m in E Africa (occasionally down to 500 m in Tanzania), above 1600 m in Sudan, 1700–4000 m in DRCongo, above 1800 m in Zambia, above 1530 m in Malawi; mainly 1400–2200 m in E Zimbabwe, above 1220 m C Mozambique, but in South Africa from sea-level (in winter) to Leucosidea scrub in alpine grassland at 3000 m.

Movement

Altitudinal migrant in dry winter season in many parts of range, especially S from Malawi, but thought normally not to move very far; e.g. mainly resident even at high altitudes in Drakensberg Mts and in Bvumba Highlands of E Zimbabwe, and no evidence of substantial movement despite considerable ringing data; only rare winter visitor to extreme S Mozambique.

Diet and Foraging

Wide variety of animal and vegetable food recorded, with opportunist use of local resource, e.g. caterpillars often taken when abundant in canopy, and termites often dominant in diet in acacia woodland; lizards and small frogs also recorded. In South Africa, of 17 stomachs and 87 faecal samples (mainly from KwaZulu-Natal), 88% held ants, 67% beetles (Coccinellidae, Curculionidae, Melolonthidae, Scarabaeidae, Staphylinidae, Tenebrionidae), 65% fruit, 46% moths and caterpillars, 35% termites, 17% parasitic wasps, 15% bugs (Naucoridae, Tingidae), 12% spiders, 10% orthopterans, 9% flies (Asilidae, Tabanidae), and 4% centipedes and pseudoscorpions; stomachs of 23 birds from throughout year (from Free State) held, by number, 37% seeds, 30% berries, 18% ants, 10% beetles, 2% plant parts, 1% unidentified larvae, 1% flies and 1% lepidopterans and bugs. Fruits consumed in Western Cape include Asparagus, Celtis, Cestrum, Ficus, Halleria, Hedychium, Ilex, Kiggelaria, Maytenus, Morus, Olea, Physalis, Psidium, Rhus, Rubus and Solanum, with seeds (including attached oil-rich funicles) of exotic Acacia cyclops. Forages mainly on ground under shrubs or in open, often in sight of mate, usually disturbing leaf litter by hopping through, rather than by using bill; perches low on branch or rock and sallies to ground and in air after prey; also gleans from foliage, twigs and trunks, and ascends to canopy for caterpillars. Follows army-ant swarms. On SW Cape coast, forages for crustacea and kelp-fly larvae in intertidal zone. Visits birdtables, taking foods such as cheese and bonemeal; raids domestic pets’ food-bowls, and recorded as entering house to peck butter.

Sounds and Vocal Behavior

Song , by both sexes (female normally shorter muted versions), a series of melodious whistled phrases, repetitive, halting and fairly high, most starting with soft, downslurred whistle, “tiiu-chiio chiio-tu-tiio tiio-tiio-tu-wiiuu”; delivery faster in N races than in S ones; mimicry variable in extent individually, non-existent to extensive, with up to 20 bird species copied. Main call a highly distinctive “wurdedur” or “garg-ga-garg” or “turr-da-da”, sometimes simply “garg”, and somewhat faster with a few more syllables N of R Zambezi, used in alarm, contact and at roost; in anxiety a soft descending “piiiiuuu”, and in distress a quiet ticking.

Breeding

Jan and Mar in Sudan; breeding-condition birds May and Jul in DRCongo; all year in E Africa, with peak in long rains and smaller peak in short rains; Oct–Jan in Zambia and Malawi; Sept–Dec (peak Oct–Nov) in Zimbabwe; breeding activity recorded in every month in South Africa, with laying peaks Aug–Sept in winter-rainfall areas and Oct–Nov in summer-rainfall areas; two broods, sometimes three, in South Africa. Territory in South Africa (maintained throughout year if not migratory) 0·05–0·75 ha, size varying with habitat. Nest construction 4–14 days, sometimes longer, an open bulky cup (with ramp at entry point in one third of cases) made of twigs, bark, dead leaves, grass stems, fronds, rootlets, seed pods and moss, lined with fine rootlets, bark, fine grass heads and/or animal hair; placed mostly in recess in earth bank, top of hollow stump, niche in tree trunk, amid shrubbery branches or in suspended flood debris along watercourse, in gardens sometimes in artificial site (e.g. old pot, box, hanging basket, roll of wire); from sample of more than 1000 nests, about one third placed on ground (but these less detectable than those above ground), mean height of off-ground nests 1·15 m, highest 3·7 m; occasional reuse of sites recorded. Eggs 2–3 (mean 2·7 for 69 clutches), white, cream, buff, pale green or pale blue, with pinkish, russet and chocolate freckles and spots; incubation period 13–19 days, mainly 16 days; chicks brooded by female for 5–11 days (period dependent on weather), nestling period 16·5–18 days (sometimes only 15 days), young barely able to fly when leave nest; post-fledging dependency at least 32–38 days, in rare cases 50 days. Brood parasitism by Red-chested Cuckoo (Cuculus solitarius) 2·46% of 1503 nests throughout S Africa, locally much higher rate, 16–22% of nests in NE South Africa. In acacia savanna in KwaZulu-Natal, ten birds fledged from 19 nests over two years, representing 21% success for eggs laid; main cause of failure predation.
Not globally threatened. Common and widespread in appropriate habitat throughout range; particularly common in e.g. Nairobi suburbs, in Kenya. In South Africa, range has expanded over the last century.
Distribution of the Cape Robin-Chat - Range Map
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  • Migration
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Distribution of the Cape Robin-Chat

Recommended Citation

Collar, N. (2020). Cape Robin-Chat (Cossypha caffra), 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.carcha1.01
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