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Plumbeous Antbird Myrmelastes hyperythrus 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

Restricted to western Amazonia, the monotypic Plumbeous Antbird is found from southern Colombia south to northern Bolivia, and east to southwest Brazil. The species occurs in the understory and on the ground of lowland forests, and is known from both seasonally flooded forests, especially those with a more open understory and at the margin of oxbow lakes, and transitional areas. Males are relatively large-bodied and predominantly dark slate-gray, with three rows of clear but relatively small white wing-spots, and a patch of blue orbital skin around the eye. Within this group of Myrmeciza antbirds, females are rather more distinctive than their partners, and in the present instance the female Plumbeous Antbird is bright rufous below, while the rest of the bird’s plumage echoes that of the male. The species is generally fairly common, but most easily located by virtue of its distinctive voice, and has been recorded up to 800 m, but is generally more abundant at lower elevations.

Field Identification

17 cm; 38–44 g. Bare periorbital skin extensive, light blue. Male is dark slaty grey; wings and tail blackish-grey, wing-coverts spotted white at tips; underwing-coverts blackish-grey. Female has upperparts like male; bright rufous below, tinged brown on flanks and crissum.

Systematics History

Previously placed in Myrmeciza, but genetic data (1) situate it in present genus (of which it is the type species), where it forms the central of three clades. Monotypic.

Subspecies

Monotypic.

Distribution

S Colombia (W Caquetá), NE Ecuador (Sucumbíos, Orellana), E Peru (Loreto S to Madre de Dios), SW Amazonian Brazil (E to R Purus drainage) and NW Bolivia (Pando, N La Paz, Beni).

Habitat

Understorey and floor of lowland evergreen forest, both seasonally flooded (várzea) and transitional; to 450 m, rarely to 750 m. Prefers shaded, more open interior of várzea, especially where small saplings and treefalls abundant; also around margins of oxbow lakes.

Movement

Presumed resident.

Diet and Foraging

Little published. Feeds on various insects and other arthropods; also on snails. Recorded prey in Brazil included hemipterans, cicadas (Cicadidae), lepidopterans, beetles (Curculionidae), spiders, and snails (Gastropoda). Closely associated pair-members, individuals, or family groups forage mostly 0–3 m above ground, usually apart from mixed-species flocks; habitually pounds tail downwards while foraging. Seeks prey on leaves and branches in dense low vegetation such as vine tangles, bamboo, Heliconia thickets, saplings and palmettos; examines bark of rotting logs and fallen palm fronds; frequently forages on the ground, probing in leaf litter, and regularly hopping up to low perches (often clings laterally to slender vertical stems) to scan for prey before hopping back down. Has been observed to search dead leaves systematically for hidden arthropods, but frequency of this behaviour not known. Prey usually perch-gleaned by reaching up, out or down with quick stabs of the bill. Observed to pick large larvae 5–8 cm long from fallen tree trunks; in order to consume these, pecked off pieces a third the size of the bill, sometimes biting pieces off ends. Occasionally follows army-ant swarms in pursuit of prey flushed by the ants.

Sounds and Vocal Behavior

Loudsong a long (e.g. 3·5 seconds) rattling trill that accelerates throughout, and gains and then declines in intensity. Calls include deep, hollow, abrupt (e.g. 0·05 seconds) “whick”, singly or, more often, repeated rapidly in doublets in which first note more intense; also a triplet of similar-quality notes, and deep raspy rattles in which first note longer and more intense.

Breeding

Single nests found in Mar (details previously unpublished) and Oct in SE Peru (Madre de Dios); nest-building seen once in Aug in Brazil (E bank of R Javari); gonadal condition of females and sightings of juveniles or fledglings indicate breeding in Apr–Dec in Ecuador (at Limoncocha). In Peru, nest a basket 16 cm long, 8 cm wide, 7·5 cm deep, made of black fern roots, dry leaves attached to exterior by spider web, one placed on and woven to two leaves of epiphytic fern c. 1 m above ground, other fern leaves covering it from above, another 0·7 m up and attached to spines of a Bactris palm; in Brazil, male gathered material from ground, made three consecutive trips in 5 minutes to same spot, incomplete nest a basket, internally 8 cm deep and 8·5 cm wide, woven entirely of blackish-brown rootlets, suspended 102 cm above ground (from bottom of nest) between two spiny understorey palms and partially supported by third, smaller palm. At Peru nest in Mar: clutch 2 eggs, pinkish, heavily streaked purple in a band; only male seen incubating, but female observed around nest.
Not globally threatened. Fairly common to common throughout most of its range. Regions occupied by this species contain several formally protected large areas, e.g. Cuyabeno Reserve, in Ecuador, Manu National Park and Biosphere Reserve and Tambopata-Candamo Reserved Zone, in Peru, Madidi National Park, in Bolivia, and Mamirauá Reserve, in Brazil, as well as privately owned properties centred around ecotourism lodges (e.g. La Selva and Sacha, in Ecuador, and Explorama, ACEER and Explornapo Lodges, in Peru). Species’ range also encompasses extensive areas of intact habitat which, although not formally protected, are at little risk of being developed in the near future.
Distribution of the Plumbeous Antbird - Range Map
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  • Year-round
  • Migration
  • Breeding
  • Non-Breeding
Distribution of the Plumbeous Antbird

Recommended Citation

Zimmer, K. and M.L. Isler (2020). Plumbeous Antbird (Myrmelastes hyperythrus), 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.pluant1.01
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