In males, the snout-vent length ranges from 14.8-18.3 mm, while in females the range is 15.8-19.8 mm. The heads are slightly wider in males than females, while females are larger overall in size. The snout is blunt and broadly rounded in dorsal view, but acutely rounded when viewed laterally, and extends past the lower jaw. The tympanum is round, and partly concealed posterodorsally. Fingers decrease in length from III>I>II>IV; the third finger is not swollen in males. The forearm is slightly longer than the upper arm, and lacks an ulnar fold. The palmar tubercle is nearly round and the thenar tubercle is elliptical, and approximately one-third the diameter of the palmar tubercle. All fingers have expanded discs and no fringes. Hands lack webbing, although basal webbing is present on the feet between toes II-IV. The dorsum is granular, with granulation increasing toward the posterior (Lima et al. 2009).
Color of the dorsum varies from light grayish brown to orange brown, often with one to several dark brown hourglass, triangular, or diamond-shaped markings. Dorsal surfaces of the arm are light orange-brown, while dorsal surfaces of the legs are light gray. Thighs, shanks, and feet have dark brown crossbars. Males have green-yellow throats with a yellow chest and belly and melanophores on the gular sac, while females have white throats with a yellow outer edge, and white chests and bellies.
No dorsolateral stripes are present. A diffuse pale tan to orangish-brown oblique lateral stripe is present, running from the midbody (sometimes starting as far forward as the arm insertion) to the groin. A ventrolateral stripe of irregular white spots runs from the anterior corner of the eye to the groin. The pupillary ring and upper iris are metallic gold with a fine black network, and the rest of the iris is brown.
Tadpole bodies are ellipsoid when viewed dorsally and flattened when viewed laterally. Larval snouts have small dorsolateral nostrils, and are bluntly rounded in both dorsal and lateral view. The spiracle is sinistral, directed dorsolaterally, located at midbody below the lateral midline, and is free. The vent is attached to the ventral fin. The upper tailfin starts at the junction of the body and tail, and the tail has robust caudal musculature. Emarginate, anteroventral oral disc, with papillae on lateral margin of anterior labium and surrounding posterior labium. Lower jaw sheath is V-shaped and both upper and lower jaw sheaths are serrated. LTRF 2(2)/3(1) (Lima et al. 2009).
Tadpoles are grayish-brown with irregular brown and silver blotches. Tadpoles of Allobates brunneus are easily distinguishable from those of the related species (A. marchesianus and A. caeruleodactylus) by the regular arrangement of papillae on the oral disc margin and irregular spots on the tail for A. brunneus (vs. unusual papillae distribution and distinct irregular stripes for the others). The oral disc of the A. brunneus tadpole has fewer surrounding papillae than that of A. subfolionidificans. The tadpole of A. nidicola has a reduced oral disc, lacks both spiracle and vent, and has yolk-filled intestines, so is easy to distinguish from that of A. brunneus. Not all Allobates tadpoles have been described (Lima et al. 2009).
Distribution and Habitat
Country distribution from AmphibiaWeb's database: Bolivia, Brazil, Colombia, French Guiana, Guyana, Peru, Suriname
Allobates brunneus is found in a number of South American countries. Populations inhabit Brazil, Bolivia (the northern tip), French Guiana (though this may refer to another species), Guyana, Suriname, and Venezuela (south of the Orinoco River only). Within the Brazilian state of Mato Grosso, this species is found in lowland swamp forests areas along the banks of the slow-running Rio Casca and its tributaries, at 300-380 meters asl (Lima et al. 2009).
Life History, Abundance, Activity, and Special Behaviors
Allobates brunneus is active during the day (diurnal). It generally lives on, or very close to the ground (Lima et al. 2009).
Males call all day, especially during periods of heavy rainfall (O600 h-1830 h), but generally mating calls are most common in the early morning (0600 h-0900 h) and late afternoon (1600 h-dusk). Calls recorded at temperatures above 28 C were sequences with groups of 6-11 notes separated by longer silent intervals. Below that temperature, notes were ungrouped and inconsistent. Males occasionally engage in wrestling bouts (Lima et al. 2009).
This species primarily lays eggs on the upper leaf surfaces of understory vegetation (10-60 cm above ground), unlike other species of Allobates, as well as occasionally inside rolled up leaves within terrestrial leaf litter. Each oviposition site has a single clutch of about 17 eggs. Tadpoles develop within the egg jelly on the upper surface of the leaf, to about stage 25 before the parent transports the larvae to small pools in the vicinity of streams.
Trends and Threats
The primary threat to Allobates brunneus is habitat loss due to increased agriculture. Other distinct threats include the construction of hydroelectric dams (primarily in Brazil), and logging and deforestation (Lima et al. 2009).
Populations are present in protected areas in Venezuela (Duida Marahuaca National Park), and Bolivia (Noel Kempff Mercado National Park).
Until 2002, a protected population could also be found in the National Park of Chapada dos Guimarães, in Brazil. However, swamp forest flooding along the Rio Casca seems to have extirpated this population. Other populations along the Rio Manso have also been extirpated due to flooding from a newly constructed hydroelectric dam and reservoir (Lima et al. 2009). In Brazil Allobates brunneus is also found within the refuges of Rondonia and Tapajós (Morales 1994).
Possible reasons for amphibian decline
General habitat alteration and loss
Habitat modification from deforestation, or logging related activities
Intensified agriculture or grazing
Dams changing river flow and/or covering habitat
Lima, A.P., Caldwell, J.P., and Strussmann, C. (2009). ''Redescription of Allobates brunneus (Cope) 1887 (Anura: Aromobatidae: Allobatinae), with a description of the tadpole, call, and reproductive behavior.'' Zootaxa, 1988, 1-16.
Morales, V. R. (1994). ''Taxonomia sobre algunos Colostethus (Anura: Dendrobatidae) de Sudamérica, con descripción de dos especies nuevas.'' Revista Española de Herpetología, 8, 95-103.
Written by Taha Jabbar (tjabbar AT berkeley.edu), UC Berkeley
First submitted 2009-02-12
Edited by Kellie Whittaker (2009-03-17)
Species Account Citation: AmphibiaWeb 2009 Allobates brunneus <http://amphibiaweb.org/species/1546> University of California, Berkeley, CA, USA. Accessed Jun 21, 2018.
Feedback or comments about this page.
Citation: AmphibiaWeb. 2018. <http://amphibiaweb.org> University of California, Berkeley, CA, USA. Accessed 21 Jun 2018.
AmphibiaWeb's policy on data use.