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Red-chested Flufftail Sarothrura rufa Scientific name definitions

Barry Taylor, Guy M. Kirwan, and Peter F. D. Boesman
Version: 1.1 — Published October 22, 2021
Revision Notes

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Field Identification

15–17 cm; male 30–46·5 (38·8) g, female 29·5–42 (36·6) g (1); wingspan c. 25 cm. Tail noticeably long, especially compared to similar to S. boehmi of wetland habitats (1); often fluffed out. In male, chestnut extends to mantle and lower breast; upperparts black with short white streaks becoming spots on greater wing-coverts and tertials; tail black, spotted white. Female paler, more golden brown, than females of other wetland or grassland flufftails, e.g. S. lugens; spots and bars predominantly buff. Bare parts: irides dark brown, bill blackish with blue-grey mandible, and legs dark grey tinged brown to pink (1). Immature resembles adult but in male chestnut is duller and white markings fewer, mostly spots, female very dark brownish black with paler, less numerous spots on upperparts and more extensive markings on underparts. Juvenile has upperparts including wings dull black, underparts dull grey-black except for whitish chin, throat and centre of belly. Males of races elizabethae and <em>bonapartii</em> have longer white streaks on upperparts, but white spots on tail and rump of bonapartii run together, appearing more streaked; upperparts of female elizabethae mainly barred, of female bonapartii mainly crescent-shaped or streaked; bonapartii smaller than both elizabethae and nominate rufa (1).

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.

Race ansorgei proposed for birds of Angola, but differences from nominate considered trivial. Three subspecies recognized.

Subspecies


SUBSPECIES

Sarothrura rufa bonapartii Scientific name definitions

Distribution

scattered records (in Liberia and Togo) from Sierra Leone E to Nigeria; more continuously in S Cameroon, Equatorial Guinea, Gabon and Congo.

SUBSPECIES

Sarothrura rufa elizabethae Scientific name definitions

Distribution

WC Ethiopia; SW Central African Republic and N and E DRCongo E to Uganda and W Kenya.

SUBSPECIES

Sarothrura rufa rufa Scientific name definitions

Distribution

C Kenya through Tanzania (including Zanzibar and Pemba I (2) ), S DRCongo and Angola to South Africa.

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

Wide range of wetland vegetation types, from seasonally wet hygrophilous grassland and sedge meadow as short as 55 cm to permanently flooded reedbeds up to 3 m tall, including papyrus swamp; normally avoids deeply flooded vegetation. In forested areas of W Africa also occurs in dry grass, sometimes near human habitation. Requires dense cover and foraging areas of mud, firm ground or short vegetation. In South Africa widespread from sea-level to 2100 m, above which altitude suitable cover does not grow; occurs up to 2700 m in Kenya and 2600 m in Ethiopia (1).

Movement

No evidence for regular movements; pairs entirely sedentary and permanently territorial when conditions permit. Very local movements occur in non-breeding season when habitat is drastically reduced, e.g. by burning or drying out. Immatures disperse widely outside breeding season.

Diet and Foraging

Takes wide variety of invertebrate prey, including earthworms, small gastropods, spiders, and adults and larvae of many insects, including termites and small ants. Seeds, mainly of grasses, eaten frequently, but not fed to chicks, and may form large part of diet in non-breeding season. Daily energy intake of adults 140–150 kJ. Forages throughout day, with peaks in early morning and late afternoon. Searches low-growing plants for insect prey; forages on dry to wet substrates, digging with bill among roots, moss and in soft ground; takes active prey on and below surface of shallow water.

Sounds and Vocal Behavior

Red-chested Flufftail prefers the wetter well-vegetated areas of marshy habitat, where it stays well hidden and therefore is far more heard than seen. Knowledge of the Advertisement and Territorial call are essential to detect the presence of this species, but detailed study revealed that the vocabulary of this species is in fact far more extensive (3,1).

Vocalizations

Vocal Development

Chicks utter quiet cheeps and a plaintive, repeated wee-ick for food begging and contact. Immatures develop a small variety of the adults territorial, alarm and contact calls. While sharing the parents territory, they frequently utter the Territorial call, which resembles more the higher-pitched version of the female.

Vocal Array

Advertisement call. A short pure whistled dove-like hoot woooo repeated at steady pace. The hoot has a duration of ⁓0.4‒0.6s, a pace of ⁓0.7-1.0 notes/s, increases in amplitude towards the end and rises slightly in pitch from about 650Hz to 800Hz. Some variants exist, such as a hoot which has a distinct sudden pitch change at the end woooah. Series may continue for a minute or more. Call is audible up to ⁓500m,

Territorial call. A rapid series of identical loud nasal notes, each rising in pitch at end dueh-dueh-dueh… Note duration ⁓0.25s, pace ⁓2.4‒2.9 notes/s, base harmonic at ⁓850Hz and third harmonic at ⁓2550Hz loudest in amplitude. At close range, an audible low-pitched gulping sound accompanies the start of every note. Call becomes more strident with increased agitation or aggression. Both male and female utter this call type, the latter at slightly higher pitch, sharper and with accent on second syllable kevic-kevic… (1). This call carries less well than the advertisement call, and is audible up to ⁓200m.

Squoo-uh. This call type, somewhat intermediate between the previous two call types, is a series of mournful hoots, each of which may abruptly shift to a low-pitched gulping sound squoo-uh..squoo-uh..squoo-uh. Note duration ⁓0.5‒0.6s, pace ⁓1‒1.5notes/s. Such series may continue for several minutes, and gulping sound may be omitted further in the series.

Ki-ki-ki. A fast series of short nasal ki notes. Note duration 0.05s, pace ⁓5notes/s.

Other. A wide variety of other calls are also given, such as hooting, squeaking, rattling, moaning, hissing, humming, buzzing, bubbling and ticking notes (3).

Geographic Variation

None documented.

Phenology

Advertisement call is mainly given during the breeding season by the male. In South-Africa, Territorial call can be heard all year, but less so during the breeding period when Advertisement call is the principal vocalisation. Males are more vocal than females, and the latter are most vocal when not breeding (3). Similarly, in Zambia Advertisement call is mainly heard from January to early May, while Territorial call has been reported in all months (4).

Daily Pattern of Vocalizing

Birds are mainly vocal during the morning and again late afternoon. During the breeding season the Advertisement call can be heard at night for long periods, from a fixed position.

Places of Vocalizing

All vocalisations are uttered from the ground, typically well concealed in marshy habitat.

Sex Differences

The Advertisement call is given by the male, the territorial call is given by both sexes with slight differences in sound, the Squoo-uh call is also assigned to the male. For a detailed list of male and female vocalisations, see (3).

Repertoire and Delivery of Songs

Vocal repertoire is very extensive. In a detailed study 113 recognizable call types were identified (many of which are subtle variants of the basic call types); these may be grouped in 8 categories based on their functions (3). Most call types (in descending order) can be linked to territorial defence, aggressive behaviour, contact, alarm, advertising, courtship and mating.

Social Content and Presumed Functions of Vocalizations

The Advertisement call indicates breeding activity of a pair in an active territory. The Territorial call is made by both members of the pair throughout the year for territorial defence, but less so at the end and after the breeding period. In the period of several weeks when breeding ends, rather the Squoo-uh call is heard, possibly a less aggressive version of territorial call when the territory is also shared with (calling) immatures. In the non-breeding period, territorial defence is equally strong (contrary to other rail species which share their habitat), and playback experiments with models lead to aggressive attack (3).

Nonvocal Sounds

None documented.

Breeding

Season indeterminate in equatorial regions; Sierra Leone, May, Jul; Nigeria, Dec; Cameroon, Mar–Jul; Gabon, Nov–Dec, Mar; Zaire, Jan–Feb, May, Jul–Aug; Angola, breeding condition May; Uganda, Oct (possibly Apr–May) (5); Kenya, May; Pemba Jan–Apr; Tanzania, Feb, Mar, breeding condition Apr, Jul; normally breeds during rains (Nov–May) in S Africa but Aug–Dec nesting recorded in SW Cape, under winter rainfall regime (Apr–Sept). As in some other Sarothrura, birds at higher altitudes may breed 1–2 months later than those at lower elevations (1). Monogamous and permanently territorial, forming strong permanent pair-bond; pairs may be spaced at intervals of as little as c. 50–100 m (1). Territory size varies little between the breeding and non-breeding seasons, c. 0·1–0·45 ha in the former period, versus c. 0·05–0·5 ha in the latter (1). Nest is a cup of grass or dead plants, sometimes with slight dome; well hidden in or under clump of grass or herbs 8–30 cm above ground or water surface; often nests in damp to shallowly flooded grass at edge of marshy areas; external diameter 13 cm, internal diameter 8–9·5 cm, depth of cup 3–4 cm. Usually 2–3 white (1) eggs (2–5), 24–29·4 mm × 17·6–21·5 mm (1), laid at daily intervals; incubation usually 16–18 days (14–18), male by day, female at night; chicks precocial and nidifugous, leave nest after 2–3 days, fed by both parents; black downy chicks have pronounced fluffy tail and black bare parts, bill with white tip and pink base; body fully feathered at 23 days; normally independent after 3–4 weeks, but may solicit food until 8–9 weeks old; remiges and rectrices fully grown at six weeks, when young fly; post-juvenile partial moult then begins, complete at 10–11 weeks. Age of first breeding one year; adult mortality low. Clutch losses, from predation or flooding, sometimes high; juvenile mortality possibly low. Usually 1–3 (1–4) broods per season; interval between clutches 4·5–9 weeks; in captivity, in Zimbabwe up to six clutches laid Aug–May. Young may help feed chicks of subsequent broods; young of last brood often remain in parental territory during non-breeding season, being ejected by start of next breeding season.

Not globally threatened (Least Concern). Widespread, sometimes locally common to abundant, e.g. in Congo, Malawi, South Africa, Zambia and Zimbabwe (1), but much less common across apparently disjunct W African range (except perhaps locally in Sierra Leone) (1) and very few records prior to 1990s in Uganda, although recent observations there suggest it is commoner than supposed (5) and it has been found in several protected areas, e.g. Kibale and Bwindi Impenetrable National Parks (6) and Echuya Forest Reserve (7). Recently recorded for first time in Ghana (8), but claimed occurrence in Ivory Coast remains unconfirmed (1). Occurs at densities of 2–6 pairs/ha in Natal, South Africa; a successful colonist of artificially created, sometimes very small, habitat patches. However, overall numbers must be decreasing with the continual destruction of wetland habitats throughout its range.

Distribution of the Red-chested Flufftail - Range Map
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  • Year-round
  • Migration
  • Breeding
  • Non-Breeding
Distribution of the Red-chested Flufftail

Recommended Citation

Taylor, B., G. M. Kirwan, and P. F. D. Boesman (2021). Red-chested Flufftail (Sarothrura rufa), version 1.1. 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.recflu1.01.1
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