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White-chinned Woodcreeper Dendrocincla merula Scientific name definitions

Curtis A. Marantz, Alexandre Aleixo, Louis R. Bevier, and Michael A. Patten
Version: 1.0 — Published March 4, 2020
Text last updated January 1, 2003

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Introduction

Seven subspecies of the exclusively Amazonian White-chinned Woodcreeper are generally recognized, but it seems plausible that the nominate subspecies and D. m. obidensis, which are both restricted to areas north of the Amazon and east of the Rio Negro, are better treated as a species apart, based on differences in their songs, size, and eye color. Over its wide range, from southern Venezuela south to northeastern Bolivia, this woodcreeper inhabits a variety of forest types, but it is principally found in terra firme and floodplain regions, and is only usually observed at the fringes of seasonally flooded forests. This obligate follower of army ant swarms, which takes most of its vertebrate and invertebrate prey on or close to the ground, appears to be uncommon over the vast majority of Amazonia, perhaps as a result of it being out-competed by many of the larger ‘professional’ antbirds at many localities over western and southern localities; where these species are absent, the White-chinned Woodcreeper seems more numerous.

Field Identification

16–21 cm; male 28–54 g, female 29–54 g (much of Amazonia), male average 57 g, female 49·5 g (Manaus). Geographic variation in size significant; birds from SE Peru slightly larger than others, and birds along N bank of Amazon R (E of R Negro) substantially so. Medium-sized woodcreeper with relatively short, straight bill, uniform-looking plumage. Nominate race is almost entirely dark reddish-brown, with wing-coverts, remiges and tail slightly more rufescent; tips of inner webs of outer primaries dark brown; narrow stripe of white to yellowish from chin to lower throat sharply defined (often difficult to see in field); underparts dark olive-brown, blending to dark rufous on undertail-coverts; underwing-coverts pale chestnut; iris reddish-brown to brown; bill brownish to black, lower mandible variably black to brown, grey, greenish, even pale yellowish to nearly white, sometimes with black tip; legs and feet bluish, olive, grey or brownish. Differs from D. fuliginosa mainly in lacking facial striping, instead appearing plain-faced apart from pale throat. Sexes similar, female may average slightly smaller. Juvenile has less contrasting throat dirty white or dingy buff, generally darker underparts, often entirely dark bill apart from obvious gape-flanges. Race obidensis similar to nominate in coloration, but significantly larger; remaining subspecies all generally paler, both above and below, with remota the palest and olivascens more olive overall; both castanoptera and badia again more rufescent, especially the latter, which also has a larger, whiter throat-stripe; bartletti differs by having dusky tips to primaries and outer secondaries; colour and extent of pale throat, and pattern of the primaries vary geographically; also eye colour, grey or blue-grey to bluish in most of range, but reddish-brown to brown in races merula and obidensis; probably more complex than this, because both brown and grey eyes noted in Roraima and Orinoco region, and one bird with brown eyes collected in northern Mato Grosso.

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.

Formerly included the taxon meruloides, now considered to be closer to D. fuliginosa. Races W of R Negro together with those S of R Amazon may constitute a separate species, on basis of differences in vocalizations, size and iris colour; more work needed. Seven subspecies recognized.

Subspecies


SUBSPECIES

Dendrocincla merula bartletti Scientific name definitions

Distribution

W Amazonia and upper R Orinoco drainage, both N and S of R Solimões, from C Venezuela and C Colombia S to E Ecuador, E Peru, N Bolivia and W Amazonian Brazil (E to R Negro and R Madeira).

SUBSPECIES

Dendrocincla merula merula Scientific name definitions

Distribution

the Guianas and adjacent N Brazil (E of R Branco in Roraima and N Pará).

SUBSPECIES

Dendrocincla merula obidensis Scientific name definitions

Distribution

Amazonian Brazil along N bank of Amazon, from R Negro E to Amapá.

SUBSPECIES

Dendrocincla merula remota Scientific name definitions

Distribution

E Amazonian Bolivia (N Santa Cruz), probably also adjacent Brazil (NW edge of Pantanal).

SUBSPECIES

Dendrocincla merula olivascens Scientific name definitions

Distribution

S Amazonian Brazil S of Amazon, from R Madeira E to R Tapajós.

SUBSPECIES

Dendrocincla merula castanoptera Scientific name definitions

Distribution

S Amazonian Brazil S of Amazon, from R Tapajós E to R Tocantins.

SUBSPECIES

Dendrocincla merula badia Scientific name definitions

Distribution

SE Amazonian Brazil from R Tocantins E to Maranhão.

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

Primarily humid forest, both terra firme and on floodplains; also forests on sandy soils in Colombia and at some sites in Brazil, and occasionally gallery, riverine or flooded forests. Prefers open understorey of interior of mature forest, less frequently subcanopy, older second growth and edges; occasionally in denser vegetation around streams, young second growth, bamboo thickets, or fringes of várzea forest. Largely restricted to forest undergrowth, using lower strata than D. fuliginosa occurring at same sites. Exclusively lowlands, generally below 300 m, occasionally to 500–600m.

Movement

Resident. Some movement within sites; even “settled” birds move over areas 2–3 km across; the sexes have overlapping territories.

Diet and Foraging

Diet consists largely of arthropods, but small vertebrates occasionally taken. Stomach contents from one site in N Bolivia mostly Hymenoptera and beetles (each comprising 33% of diet), with fewer spiders (19%) and Orthoptera (14%); other items rarely taken. Stomachs from other sites in N Bolivia and from E Peru contained primarily orthopterans, spiders and ants, with lesser numbers of beetles, cockroaches (Blattodea), bugs, vertebrates; those from Amazonian Brazil contained Hemiptera, Coleoptera, Blattaria, Isoptera, and even Odonata. Comparison of stomach contents with prey flushed by army ants revealed orthopterans are taken preferentially, with cockroaches and, especially, Hymenoptera avoided. May select prey of small to moderate size, possibly larger than taken by some other dendrocolaptids; 21% of items smaller than 7 mm, 65% were 8–16 mm, and 14% over 16 mm. Substantial overlap with other woodcreepers and several ant-following antbirds (Thamnophilidae) in both type and size of prey taken; however, this and other ant-following dendrocolaptids may take smaller items than antbirds, in relation to bill size, because they have more difficulty in removing appendages before eating prey. Prey observed taken over swarming army ants include, in decreasing order of abundance, cockroaches, spiders, ant larvae, centipedes (Chilopoda), scorpions, crickets (Gryllidae), grasshoppers (Acrididae); beetles, moths, skippers (Hesperiidae), whipscorpions (Amblypygi) and lizards all taken only on occasion. An obligate ant-follower, forages mostly over Eciton burchelli, also regularly over Labidus praedator; may visit multiple ant swarms on same day, and monitors inactive colonies; radio-tracked female with nestling routinely travelled over 300 m between ant swarms, suggesting that movements of over 500 m from nest to foraging sites perhaps not uncommon. Typically, 1–2 individuals present at swarms in Brazilian Amazon, but up to 7–8 seen at swarms in SE Peru; larger groups probably involve wandering immatures, aggregates of solitary birds, or females with young. Perches lower and often on slimmer trunks than do other woodcreepers, rarely more than 3 m above ground, often using trunks with diameter less than 15 cm. Foraging methods vary depending on presence of large antbirds such as Black-spotted Bare-eye (Phlegopsis nigromaculata). In Brazil, nearly 90% of all foraging is within 1 m of ground in absence of Phlegopsis near Manaus, where regularly remains relatively motionless on slimmer and more angled perches, but near Belém, where Phlegopsis present, only 58% of foraging below 1 m, birds move about more over ants, and they forage mostly from larger (6–15 cm diameter), near-vertical trunks. Suggested correlation between body size of these woodcreepers and presence of large antbirds not supported by small size of birds in Roraima, where large antbirds are absent. Rarely hitches far up trunks, instead flying between perches. Most prey taken by rapid sallies to ground, followed by return to perch; sallies occasionally to foliage, rarely to other substrates. Seldom picks or gleans prey from trunks or foliage. Has been observed to perform “anting”, but rarely flicks wings to flush prey. Highly aggressive towards both conspecifics and other species over ants, usually supplanting smaller species and being supplanted by larger ones; dominant over D. fuliginosa, often excluding it from foraging low over swarms, or forcing it to forage away from them. Rarely seen away from ants; at such times moves rapidly and silently through understorey, apparently in search of new swarms. Rarely follows mixed-species flocks away from ants. Radio-tracked birds observed to forage also in association with herds of peccaries (Tayassu pecari), which flush prey much as do swarming ants; one individual even seen perched atop hindquarters of a peccary.

Sounds and Vocal Behavior

Calls often heard near ant swarms, but songs poorly known; both vary geographically. Most frequent vocalization a multi-note chatter call, often given at ant swarms, usually 2–4 notes, described as “dit-it-it-it” or “tat-at-at” over most of range, but piercing “deet-eet-ee” in N Amazonia E of R Negro. Song in Manaus area (Brazil) a series of 6–9 loud, whistled notes described as “kew, kew, kew, kew, kew, kewp”, but over most of range apparently lower in frequency and described as “we, wi, di, dit”, or “wi-wid-wid-di” in SE Colombia, and in some places an ascending whistle of 2–3 notes. Other calls include sharp “spee” notes in Manaus area, growling “chauhhh”, long rattle at 4–5 notes per second (i.e. slower than D. fuliginosa), quiet “wi-i-i-i-ih” rattle, also “tsiriRIT” possibly as warning call.

Breeding

Little known. Birds in breeding condition in Feb–May in NW Brazil, E Colombia and S Venezuela, in late Jun in NE Amazonian Brazil (Amapá) and in mid-Aug in S Amazonian Brazil (Mato Grosso), and in non-breeding condition in early Oct in NE Amazonia; fledged juveniles of obidensis mid-Jul to mid-Oct, but juvenile specimens of other races mostly May–Jul; in W Amazonia, juveniles appear at ant swarms in Dec–Jan (SE Peru) and adults in moult in Oct–Apr; birds moulting in Apr in upper R Orinoco region and in worn plumage in Sept in French Guiana, suggest breeding during dry season; more work needed to confirm geographical component to variation in season. Pair-bond apparently brief; male and female associate irregularly, and for only c. 1 month, but may investigate nesting cavities together. Nest undescribed, apparently in cavity. No details on clutch size and eggs; DNA analysis revealed that female alone raises young and associates with them after fledging; male lacks brood patch, and not observed to attend young; fledglings remain with parent for 3 months (until late Jan or early Feb near Manaus), but often stay in area longer (two still present in following May); one, rarely two, dependent young encountered with single parent. Nest predation suggested as less than 80% over a breeding season of 3–6 months. Adult survival relatively high, with average annual survival 71% over 3-year period (10 of 26 birds resighted 3 years after initial capture); one bird recaptured at another site after 4 years.
Not globally threatened. Locally common, but apparently uncommon over much of range. Abundance may be depressed through competition over ants by larger thamnophilids; densities possibly lower in S & W Amazonia where Phlegopsis and Rhegmatorhina present, but fairly common to common in absence of those species near Manaus and at sites in both Rondônia and Roraima; uncommon in Amapá and Guyana in absence of large antbirds, but rare at Belém in their presence. Only one record from Surinam, in 19th century; uncommon in French Guiana and N Bolivia; scarce and possibly local in Venezuela; fairly common to common in W Amazonian Brazil and adjacent Peru; uncommon in NW Mato Grosso, but quite rare at well-worked Alta Floresta (NC Mato Grosso); rare in NE Ecuador. Density at site in floodplain-forest in SE Peru 16–22 birds/100 ha, with average home range over 64 ha; at Manaus 2·5 birds/100 ha considered an annual low, with 3·6 birds/100 ha representing peak (post-breeding) density. Like other obligate ant-followers, highly sensitive to fragmentation and disturbance of mature forest, all but disappearing from fragments up to 100 ha in size, and apparently requiring 200–400 ha to survive; birds experimentally introduced into 10-ha fragments lacking army ants left within 48 hours, many sooner, and capture rates dropped effectively to zero in fragments smaller than 10 ha. Gaps shown not to be an insurmountable barrier, despite significantly reducing bird movement; marked birds crossed 75–100 m of open space between fragments and continuous forest (not only to abandon fragments, but also occasionally to visit them when scouting for swarming ants). Trapped while moving through second growth dominated by both Vismia and Cecropia in approximately equal numbers, and apparently able to use regenerating forest to move between patches of better habitat. Often abandons ant-swarms that move into second-growth, and always those that enter clearings. Even relatively low levels of selective logging may have significant impact on this and other dendrocolaptids. An indicator species for tropical lowland evergreen forest in both N & S Amazonia.
Distribution of the White-chinned Woodcreeper - Range Map
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  • Year-round
  • Migration
  • Breeding
  • Non-Breeding
Distribution of the White-chinned Woodcreeper

Recommended Citation

Marantz, C. A., A. Aleixo, L. R. Bevier, and M. A. Patten (2020). White-chinned Woodcreeper (Dendrocincla merula), 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.whcwoo1.01
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