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Black-bellied Antwren Formicivora melanogaster Scientific name definitions

Kevin Zimmer and Morton L. Isler
Version: 1.0 — Published March 4, 2020
Text last updated January 1, 2003

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Introduction

Despite this species’ undoubtedly large range across eastern and central South America, it is almost endemic to Brazil, as the Black-bellied Antwren only narrowly extends into northern Paraguay and southeast Bolivia. Throughout its distribution, the species is fairly common, although it is perhaps more sensitive to habitat degradation than some of the Caatinga’s other avian inhabitants. In plumage, the Black-bellied Antwren recalls the partially sympatric White-fringed Antwren (Formicivora grisea), but males are rather darker above, with much less obvious white flanks, while females are even more easily separated by the broad white supercilium contrasting with the dark mask, and paler underparts. The Black-bellied Antwren is typically found in pairs in the under- or midstory of taller caatinga, tropical deciduous woodland, or even second growth at the ecotone between caatinga and cerrado.

Field Identification

12–13 cm. Male nominate race has broad white supercilium, dark greyish-brown crown and upperparts, crown feathers with blackish centres, outer scapulars edged white, concealed white interscapular patch; wings blackish, coverts tipped white; graduated tail black, sides white, white tips on central feathers, white tips becoming larger towards outer rectrices; white of supercilium extending in a line to breast side and broadening on flanks; head side, throat and remaining underparts black, underwing-coverts white. Distinguished from very similar F. grisea by broader supercilium, especially behind eye, less white on flanks. Female differs from male in browner crown and upperparts, interscapular patch reduced or absent, broad black eyeband contrasting with white throat, faintly buff-tinged white underparts. Race bahiae is paler above, tail with smaller white spots, wider white line connecting supercilium and flanks on male.

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.

Forms a clade with F. serrana. Two subspecies recognized.

Subspecies


SUBSPECIES

Formicivora melanogaster bahiae Scientific name definitions

Distribution

NE Brazil (extreme E Maranhão E to Rio Grande do Norte, S to N Bahia and W Pernambuco).

SUBSPECIES

Formicivora melanogaster melanogaster Scientific name definitions

Distribution

C Brazil (S Mato Grosso E to S Bahia, S to W Mato Grosso do Sul, W São Paulo and N Minas Gerais), SE Bolivia (Santa Cruz, Chuquisaca, Tarija) and extreme N Paraguay (Alto Paraguay).

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 and mid-storey of tropical deciduous forest (including mata-de-cipó vine forest) and taller caatinga scrub, from lowlands to 1050 m. Also ventures into degraded caatinga with taller second-growth scrub, as well as ecotones between caatinga and cerrado.

Movement

None recorded; presumed resident.

Diet and Foraging

Little published. Feeds on variety of insects, including orthopterans and lepidopteran larvae, and spiders. Closely associated partners, individuals, or family groups forage mostly 0–3 m above ground, regularly to 6 m in dry forest in N Minas Gerais (Brazil), alone or, sometimes, with mixed-species flocks. Forages actively, mostly in dense thickets of deciduous shrubs and vine tangles, progressing by short hops and fluttery flights, separated by frequent pauses of 1–2 seconds to scan for prey; posture horizontal, partially fanned tail habitually swung from side to side, both wings shallowly flicked. Moves erratically, in zigzag progression with frequent abrupt changes of direction and retracing of routes; works small areas thoroughly before moving on; hitches from side to side up vertical stems. Perch-gleans prey from leaf, stem, vine and branch surfaces, by reaching out, up or down with quick bill-stabbing motions or by short horizontal lunges; also makes short (less than 40 cm) sallies and hover-gleans to vegetation, vines and branches; in mata-de-cipó woodland regularly forages within large terrestrial bromeliads, probing beneath leaf litter trapped by the blades; also regularly drops to ground to forage in leaf litter, using bill to poke underneath leaves and occasionally to flip smaller ones. Sometimes investigates suspended arboreal dead leaves, but just as often ignores them. Prey capture typically followed by vigorous wiping of the bill on a branch. Smaller prey immediately swallowed; larger items repeatedly bashed against branches before being consumed. Not known to follow army ants.

Sounds and Vocal Behavior

Loudsong a monotonous series resembling that of F. grisea, but pace very slow (e.g. 14 notes, 6 seconds), sometimes becoming irregular. Calls include a short series of complaining squeals (e.g. 5–15 notes at 5 notes per second), variable in frequency and pace; also sharp high-pitched “seek” notes and lower-pitched, short downslurred notes; calls may vary regionally.

Breeding

In Brazil, nest with young in Pernambuco and another in earliest stages of construction in Bahia (both previously unpublished), both in Jan. Nest was an open cup 8 cm in height (from bottom to highest point of attachment), external diameter 6 cm, inside depth 3 cm, thinly woven, lined with fine grass fibres and stems, secured with spider webs around edges, suspended by rim from horizontal fork of dead branch (and further secured by fibres at one end of rim looping over a branch crossing over fork), distance from bottom of nest to ground16 cm; fork was among cluster of thin, dead branches of a woody shrub, surrounded by scattered forbs, and with shading canopy of bare woody vines and branches 1 m above nest. Contained 2 nestlings, one obviously larger than the other, mouth-lining rich golden-yellow; fed by both parents; after one feed, female removed a faecal sac, flew low for 5–6 m, took several short hops on ground, then dropped sac and proceeded to wipe bill on a branch, before resuming foraging.
Not globally threatened. Fairly common throughout most of its range. Reliance on deciduous forest and caatinga makes it more sensitive to disturbance than are some congeners which occupy a variety of disturbed, secondary habitats. Much of region in which it occurs lacks formal protection. The dry forests, caatinga scrub and mata-de-cipó woodlands favoured by this species are being rapidly cleared for cattle pastures and coffee plantations; even where such habitats not being cleared, they are heavily exploited by local people for firewood and fence-post production, with grazing by cattle and goats preventing regeneration of most of the woody plants. The mata-de-cipó woodlands of Bahia (Brazil) harbour a high proportion of endemic and threatened species, yet they remain unprotected; establishment of one or more reserves with this habitat (preferably in Jequié-Boa Nova region) should be given high priority. In addition to preserving some of Brazil’s most threatened endemics, creation of such reserves would have added benefit of protecting large populations of more common dry-habitat birds such as present species.
Distribution of the Black-bellied Antwren - Range Map
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  • Year-round
  • Migration
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  • Non-Breeding
Distribution of the Black-bellied Antwren

Recommended Citation

Zimmer, K. and M.L. Isler (2020). Black-bellied Antwren (Formicivora melanogaster), 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.blbant2.01
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