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Lunulated Antbird Oneillornis lunulatus 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

The Lunulated Antbird occupies a rather small range in westernmost Amazonia, north and west of the river’s headwaters, in eastern Ecuador to east-central Peru, and is found in the understory of humid evergreen forest, principally in seasonally flooded areas, unlike its presumed sister-species, the White-throated Antbird (Gymnopithys salvini). The latter was occasionally treated as a subspecies of the Lunulated Antbird in the past, but in addition to their different habitat preferences and clear differences in loudsongs, males of the present species are overall darker and lack any white tail barring, while females virtually replicate the male pattern, except that brown replaces the gray body color, and there is some pale spotting and dark scalloping over the wings, back, and underparts. Like the White-throated Antbird, this species appears to be an obligate ant-follower, and many aspects of its feeding behavior are very similar to those of the latter. In contrast, its breeding biology is virtually completely unknown, and the nest has never been described.

Field Identification

13–13·5 cm; 22–26 g. Male is mostly grey, except for white supercilium, anterior ear-coverts, chin and throat; tail blackish-grey. Differs from similar O. salvini in slightly darker coloration, unbarred tail. Female has white supercilium, darker posteriorly, dark olive-brown lores and postocular patch, white subocular area and throat; crown and upperside yellowish olive-brown, back feathers, tertials and wing-coverts edged ­blackish and light buff at tips, tail dark greyish-brown, barred whitish on inner webs; underparts olive-brown, yellowest and palest on centre of breast; underwing-coverts olive-brown. Juvenile male is like female, but lacks supercilium, throat patchily white.

Systematics History

Has been treated as conspecific with O. salvini. Monotypic.

Subspecies

Monotypic.

Distribution

E Ecuador (Sucumbíos, Orellana, Pastaza, Morona-Santiago) and N & C Peru (W of R Napo and R Ucayali).

Habitat

Understorey of humid evergreen forest, primarily in seasonally flooded várzea and adjacent transitional forest; mostly below 400 m, locally to 950 m.

Movement

Presumed resident.

Diet and Foraging

Feeds on a variety of arthropods. Recorded prey include crickets (Gryllidae), cockroaches (Blattidae), ant larvae (Formicidae), spiders. Several records of individuals eating larvae of non-army ants as these carried by workers fleeing approaching army-ant swarm; one female noted to pick 21 ant larvae, and a male and young male seen to take 47. Largest recorded items c. 22 mm. Pairs, individuals, or family groups forage mostly below 1 m; does not follow mixed-species flocks, but often forages 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, attending swarms of Eciton burchelli, E. rapax and Labidus praedator; up to 10 individuals reported at a swarm, but single pair or family much more common. Early in morning, cruising individuals, pairs or family groups work through the forest 0·5–3 m above ground, flying up to 15 m at a time, alighting for a few seconds to peer about, then moving on; frequently checks ant raiding paths and bivouac sites from previous day and then, if not successful, wanders more widely, immediately investigating vocalizations of conspecifics and of other obligate ant-followers; once located, swarms are generally followed for most of 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 one extended) to thin (mostly 1–3 cm) vertical stems, where it pitches, yaws and pivots, or sidles skilfully up and down; also 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, short sallies to air, or 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 a quick stab of the bill or by a 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 thamnophilids; when large item taken, it is shaken and mandibulated, but not held with the feet or bashed against substrate; also, less often dissects prey than do G. leucaspis and G. rufigula or Phlegopsis and Rhegmatorhina; bill-wiping following prey consumption also less common than in species that regularly take larger prey. In general, less active and conspicuous than other obligate followers at ant swarms, probably reflecting its more subordinate status; more sedate and given to perching for longer periods at a single station, often within tangles of fallen branches. Dominates smaller, non-obligate ant-followers such as Hylophylax naevius, Willisornis poecilinotus and Myrmoborus myotherinus at swarms, and occasionally displaces larger White-chinned Woodcreeper (Dendrocincla merula), but clearly subordinate to larger species such as Phlegopsis erythroptera and P. nigromaculata, Hafferia fortis, Rhegmatorhina melanosticta, and its congener Gymnopithys leucaspis; often displaced by larger species to peripheral or higher zones around swarms of Eciton burchelli; two individuals of present species, thus displaced, were noted as “stealing” prey carried by army ants. More likely than larger obligate ant-followers to attend smaller swarms of less preferred ants such as Labidus praedator or Eciton rapax, where only likely competitors are smaller subordinates such as Willisornis poecilinotus or occasional Pithys albifrons. Intraspecific aggression common when two or more pairs or families attend a swarm, but aggression usually less vocal and sustained than among other obligate ant-followers; females always supplant their mates, never the reverse, and mates seldom forage less than 1–2 m apart unless male is courtship-feeding female. As young begin to feed themselves and start moulting into adult plumage, they are often dominant over their own parents and other adults at swarms, frequently supplanting adults without eliciting a display or challenge; subadults unescorted by parents apparently lose some of these privileges.

Sounds and Vocal Behavior

Loudsong a series (e.g. 12 notes, 3·3 seconds) in which unmusical “chip” notes gradually lengthen and flatten into long mellow whistles that finally fall in pitch. Calls include long and usually interrupted “chirr” and abrupt “chup”.

Breeding

Little known. In Peru (Yarinacocha), fledglings common in late Dec and early Jan, season speculated as approximately Oct–Apr on basis of presence of young and timing of rainy season. Male observed to courtship-feed female. Most pairs escorted and fed 2 young; recently fledged young remain in hiding within vine tangles and other cover, where each parent fed one fledgling and ignoring the other.

Not globally threatened (Least Concern). Rare to uncommon throughout most of its small range. Occurs in a number of privately protected areas centred on ecotourist lodges and camps in lowlands of E Ecuador, e.g. Sacha, La Selva, Cuyabeno, Yuturi and Kapawi Lodges, and Tiputini Biodiversity Station; also in the large Yasuní National Park. In Peru, presence confirmed in Cordillera Azul National Park and probably also occurs in Pacaya-Samiria National Reserve; at least formerly fairly common at Yarinacocha (Loreto), but this area is not protected. More accurate estimations of this species’ distributional limits and population centres are needed. Considered to be of high sensitivity to human disturbance. Although its habitat is at present relatively intact, much of E Ecuador has been opened up for oil exploration and drilling, and the road-building and subsequent human colonization and environmental degradation that inevitably follow could place this species at risk in the future. Its total population may be relatively small, and it is known from only a few formally protected areas.

Distribution of the Lunulated Antbird - Range Map
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Distribution of the Lunulated Antbird

Recommended Citation

Zimmer, K. and M.L. Isler (2020). Lunulated Antbird (Oneillornis lunulatus), 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.lunant2.01
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