- White-throated Antbird
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White-throated Antbird Oneillornis salvini Scientific name definitions

Kevin Zimmer and Morton L. Isler
Version: 1.0 — Published March 4, 2020
Text last updated September 5, 2018

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Introduction

Sometimes treated as conspecific with the Lunulated Antbird (Gymnopithys lunulatus), which replaces the present species in the north and west of upper Amazonia. The White-throated Antbird occurs fairly commonly across southwest Amazonian Brazil to eastern Peru and north-central Bolivia, within which range it inhabits the understory of lowland terra firme and floodplain forests. This species regularly, perhaps habitually, follows army ant swarms, foraging in pairs, small family groups, or alone, albeit with other obligate ant-following birds; it is dominant over most of the smaller species attending such events, but clearly subordinate to the larger ‘professional’ antbirds. Broadly speaking, male White-throated Antbirds are medium gray with a gleaming white throat and slightly less noticeable supercilium, separated by dark lores, and white-barred tail, while females are predominantly tawny-cinnamon, with some spotting and dark scalloping over the wings and back, and exhibit a narrowly dark-barred tail. However, there is quite considerable intra-populational plumage variation in this species, especially in females.

Field Identification

13–13·5 cm; 22–28 g, mean 25·9 g. Male is mostly grey  , wings somewhat darker, except for white supercilium, anterior ear-coverts, chin and throat ; tail barred blackish-grey and white; underwing-coverts grey. Distinguished from O. lunulatus by barred tail, slightly paler plumage. Female  has crown centre dark olive-brown with faint rufous scaling, nape, head side, throat and upper breast rufous; mantle olive-brown, becoming lightly barred black and rufous on back, rump reddish yellow-brown; remiges broadly edged rufous, wing-coverts and tertials brown, edged rufous; tail rufous, thinly barred black; posterior underparts reddish yellow-brown, becoming olive-brown on flanks; generally darker, with more heavily barred upperparts, in N (“<em>maculatus</em>” ). Subadult male  is dark grey with brown wings, throat patchily white.

Systematics History

Has been treated as conspecific with O. lunulatus. Birds in NW of range (E Peru E to R Purus, in Brazil) sometimes separated as race maculatus, but they intergrade with other populations; plumage shows high degree of individual variation in all populations. Monotypic.

Subspecies

Monotypic.

Distribution

E Peru (S of R Amazon and E of R Ucayali, S to drainage of R Madre de Dios), SW Amazonian Brazil (E to R Madeira, S to Acre) and NW & C Bolivia (Pando, La Paz, Beni, Cochabamba).

Habitat

Understorey of humid evergreen forest, to 450 m. Occurs in terra firme, transitional forest and floodplain-forest.

Movement

Presumed resident.

Diet and Foraging

Feeds on variety of arthropods. Recorded prey include orthopterans, termites (Isoptera), ant larvae (Formicidae), spiders; several records of individuals eating larvae of non-army ants as these were carried by workers fleeing approaching army-ant swarm. Largest recorded prey items recorded c. 22 mm. Forages as pairs, individually, or in family groups, mostly below 1 m; does not follow mixed-species flocks, but often in presence of other species at ant swarms, and may then be displaced to heights of 3 m by dominant ant-following species. Considered an obligate army-ant follower, recorded as following swarms of Eciton burchelli and Labidus praedator; although up to 7 individuals reported at one swarm, seldom forms big concentrations, and a single pair or family is much more common. Early in morning, cruising individuals, pairs or family parties work through the forest 0·5–3 m above ground in search of ants, flying up to 15 m at a time, alighting for a few seconds to peer about, then moving on; frequently, first checks raiding paths and bivouac sites of ants from the previous day and, if not successful, wanders more widely, immediately investigating vocalizations of conspecifics as well as those of other obligate ant-followers; once located, swarms are generally followed for most of the day. Progresses by hops and short, fluttery flights; tail regularly lowered slowly to as much as 80 degrees below plane of body, then rapidly flicked upwards to 10 degrees or more above body level. Perches mostly 0·1–0·7 m above ground, often clinging laterally (upper leg flexed, lower leg extended) to slender vertical stems mostly less than 3 cm thick, and pitching, yawing and pivoting, or sidling adeptly up and down; routinely uses horizontal perches on fallen branches, root buttresses, and stilts of stilt-rooted trees. Most attack manoeuvres are short sallies or sally-pounces to the ground, followed by quick hop back up to a perch before ants can counter-attack; less frequently makes short aerial sallies, or sallies to vines, lianas, logs, aerial roots, branches or foliage. Often perch-gleans prey from ground, stem, branch, root or vine surfaces, by reaching out, up or down with quick stab of the bill or by short horizontal lunge; this behaviour more common than among G. leucaspis and G. rufigula or other obligate ant-followers. Large prey taken less often than by other obligate ant-following antbirds; when large item taken, it is shaken and mandibulated, but not held with the feet or bashed against substrate; dissects prey less commonly than do most congeners or Phlegopsis and Rhegmatorhina; bill-wiping following prey consumption also less common than among species that regularly take larger prey. In general, less active and conspicuous at ant swarms than are other obligate followers, this possibly an adaptation to avoid aggression from more dominant species. Dominates smaller, non-obligate ant-followers such as Hylophylax naevius, Willisornis poecilinotus and Myrmoborus myotherinus at ant swarms, and recorded as occasionally displacing even the larger Plain-brown Woodcreeper (Dendrocincla fuliginosa), but clearly subordinate to larger obligate ant-following thamnophilids such as Phlegopsis erythroptera, Rhegmatorhina melanosticta and Hafferia fortis; often displaced by larger species to peripheral or higher zones around swarms. Intraspecific aggression common when two or more pairs or family groups attend a swarm, and subordinate birds are similarly displaced to higher or more peripheral stations; females always supplant their mates, never the reverse, and mates seldom forage less than 1–2 m apart unless male is courtship-feeding female. Twice observed at colonies of termites that were swarming or moving the nest above ground, and carrying soft-bodied (up to 1 cm) larvae; from low perches on stems or on a log, the birds rapidly picked larvae off the ground and devoured them, taking up to 34 in rapid succession, then moved away for a while before returning to attack the swarm, sometimes pushing over leaves to uncover larvae.

Sounds and Vocal Behavior

Loudsong a series (e.g. 6 notes, 4 seconds) of long whistles with little space between, typically individual notes ascend slightly in pitch with sharper upslur at end, while overall each note drops in pitch, and final note(s) of lower intensity, but number of notes highly variable (2–10); variant of loudsong (perhaps a distinct vocalization) with all notes except, typically, the initial one harsh and unmusical. Calls include abrupt “chup” and much longer “chirr”.

Breeding

Little known. Two nests found in Nov in Peru (Madre de Dios); young following parents in Mar–Apr at two sites in W Brazil. Nest constructed entirely of narrow strips of dry palm-frond leaflets, or pieces of palm fronds 3–5 cm long, one nest shaped into a cup but the other not; located in hollow palm stump rising 41 cm and 44 cm from forest floor, floor of nest-cavity c. 15 cm below top of stump; stump 9·7 cm and 6·8 cm in diameter, one in a small patch of Heliconia/Marantaceae plants c. 1·5 m tall. Clutch 2 eggs, light pink, maroon speckling concentrated at blunt end.

Not globally threatened (Least Concern). Fairly common throughout its relatively small range. This includes some large protected areas, e.g. Manu National Park and Biosphere Reserve and Tambopata-Candamo Reserved Zone, in Peru, Serra do Divisor National Park, in Brazil, and Madidi National Park, in Bolivia; also extensive areas of intact habitat, particularly in Brazilian part of range, which are unprotected but appear to be at little near-term risk of development. Considered to be of high sensitivity to human disturbance.

Distribution of the White-throated Antbird - Range Map
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  • Year-round
  • Migration
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  • Non-Breeding
Distribution of the White-throated Antbird

Recommended Citation

Zimmer, K. and M.L. Isler (2020). White-throated Antbird (Oneillornis salvini), 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.whtant1.01
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