Vitreorana uranoscopa
Humboldt�s Glass Frog, r�-de-vidro, perereca-de-vidro, pererequinha-verde de ventre transparente com focinho espatulado
family: Centrolenidae
subfamily: Centroleninae

© 2015 Sandra Goutte (1 of 15)

  hear call (4533.3K WAV file)

[call details here]

Conservation Status (definitions)
IUCN (Red List) Status Least Concern (LC)
Other International Status Least Concern (LC).
National Status Not listed (
Regional Status Rio Grande do Sul: Vulnerable, Paran�: Data Deficient, S�o Paulo: Probably endangered, Rio de Janeiro: Endangered


View distribution map using BerkeleyMapper.


Vitreorana uranoscopa is a small glass-frog (SVL 19,5 - 25,8 mm). The snout in dorsal view is rounded and spatulate, truncated in lateral view; upper lip with a dermal ridge; vomerine teeth are absent. Eyes directed forward, latero-dorsally located. Nostrils almost terminal. The small tympanum is covered above, distinct below, diameter about � eye diameter. Males with a single vocal sac, and vocal slits. The finger and toe discs are truncate and larger than tympanum; glandular pad on inner side of thumb. Subarticular tubercles distinct and single. A small inner metatarsal tubercle. Distinct forearm fold, shallowly scalloped or not. Dorsal texture smooth or very weakly granular; belly smooth with transparent ventral skin through which the internal organs are visible. Intricate ornamentation involving enameled tubercles, folds, and crenulated flaps. The bones are green in life (Taylor and Cochran 1955; Cei 1980; Heyer 1985; Heyer et al. 1990; Cisneros-Heredia and McDiarmid 2007). Cisneros-Heredia and McDiarmid (2007) provided a brief overview of the internal morphology.

The tadpoles are typical of those from brooks, where they are found burrowing in the leaf litter, mud, sticks and sand at the stream bottom, usually near turbulent waters. The oral apparatus is anteroventral, oral disc emarginate, LTRF 2(2)/2, 2(2)/2(1) or 2(2)/3, denticles very small, rows often incomplete. Single row of papillae. The body is ovoid in dorsal view with a narrow and muscled tail. Fins low, dorsal fin originates at the body-tail juncture. The eyes and nostrils are dorsal and very small. Spiracle sinistral, mid-way on side, posterior about 4/5 distance on side. Length at Gosner stage 41: 46.7 mm. The color in life varies from light red to yellowish (Heyer 1985; Altig and McDiarmid 1999).

Distribution and Habitat

Country distribution from AmphibiaWeb's database: Brazil


View distribution map using BerkeleyMapper.
V. uranoscopa lives associated with low flowing forest streams (or near waterfalls) on primary forests, and is less commonly found on secondary growth and forest edges. The species is distributed along the Atlantic Rain Forest (Semi-deciduous Atlantic Forest, Floresta Ombr�fila Mista and in the Floresta Ombr�fila Densa) in the Serra do Mar and Serra da Mantiqueira in the States of Esp�rito Santo, Rio de Janeiro, Minas Gerais, S�o Paulo, Paran�, Santa Catarina, and Rio Grande do Sul in eastern Brazil, and in the provincia de Missiones in Argentina up to 1,200 m (Heyer 1985; Carvalho-e-Silva et al. 2008).

Known from eastern Brazil, along eastern S�o Paulo, Esp�rito Santo, Rio de Janeiro, eastern Minas Gerais, Paran�, Santa Catarina and Rio Grande do Sul reaching northern Provincia de Missiones, in Argentina.

Life History, Abundance, Activity, and Special Behaviors
Vitreorana uranoscopa is found in forests near small to moderate streams with rocky bottoms. The adults frequently occur at low densities, usually one per 500m of stream, with a peak abundance of four calling males (Canelas and Bertoluci 2007). Lucas et al. (2008) recorded five individuals in the reproductive season along 100 m of a forest stream in central Rio Grande do Sul. Hartmann et al. (2005) reported visual signaling in this frog. Males performed limb lifting, apparently used to defend territory, then avoiding physical combat, as seen in other taxa of glass-frogs. Males call at night on low vegetation (from 150 cm up to 2.5 m above ground) and shrubs in the rainy season from August to January (Heyer et al. 1990); or November to March, according to Canelas and Bertoluci (2007), who noticed a pronounced peak in breeding in December (Cerezoli 2008) and inferred that this species is an explosive breeder. The advertisement call was described by Heyer (1985) and can be heard in Haddad et al. (2003). The call is given sporadically; call duration 0.04-0.1 s. Dominant frequency between 4500-5000 Hz, 3-6 pulses per note.

This species lays a single layer of a few eggs (often 29-32) directly on the upper surface of leaves hanging above streams. Upon hatching, the tadpoles fall into streams where they continue development (Mode 25 of Haddad and Prado 2005; Izecksohn and Carvalho-e-Silva 2001).

V. uranoscopa and H. eurygnathum co-occur in two localities of southeastern Brazil, but according to Heyer (1985) there is a divergence in habitat use between these frogs: H. eurygnathum is found in narrow streams and rivulets, while V. uranoscopa is found in wider ones. This suggestion remains to be confirmed.

Trends and Threats
Its range is within protected areas, like Parque Nacional da Serra da Bocaina, S�o Jos� do Barreiro-SP, Parque Estadual da Serra do Mar, Ubatuba-SP, Parque Estadual de Caetetus, at G�lia-SP, Parque Nacional da Tijuca, at Rio de Janeiro-RJ, Reserva do Patrim�nio Natural Serra do Cara�a, at Catas Altas-MG, Reserva Rio das Pedra, at Mangaratiba-RJ, RPPN Salto Morato, at Guaraque�aba-PR, Parque Estadual Mata dos Godoy, and at Londrina-PR, Floresta Nacional de Chapec�, at Chapec�-SC. Recent analysis did not detect infection by the fungus Batrachochytrium dendrobatidis (Carnaval et al. 2006). There are reports of population declines in the surroundings of Rio de Janeiro (Izecksohn and Carvalho-e-Silva 2001), but there were not continuous surveys in the area, and this information may not reflect the real situation (Eterovick et al. 2005).

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
Subtle changes to necessary specialized habitat
Habitat fragmentation


Altig, R., and McDiarmid, R. W. (1999). ''Diversity: familial and generic characterization.'' Tadpoles: The Biology of Anuran Larvae. R. W. McDiarmid and R. Altig, eds., The University of Chicago Press, Chicago.

Canelas, M. A. S., and Bertoluci, J. (2007). ''Anurans of the Serra do Caraça, southeastern Brazil: species composition and phenological patterns of calling activity.'' Iheringia, 97, 21-26.

Carnaval, A. C. O. de Q., Puschendorf, R., Peixoto, O. L., Verdade, V. K., and Rodrigues, M. T. (2006). ''Amphibian chytrid fungus broadly distributed in the Brazilian Atlantic rain forest.'' EcoHealth, 3(1), 41-48.

Carvalho-e-Silva, A. M. T., Silva, G. R., and Carvalho-e-Silva, S. P. (2008). ''Anuros da Reserva Rio das Pedras, Mangaratiba, RJ, Brasil.'' Biota Neotropica, 8(1), 199-209.

Cei, J. M. (1980). ''Amphibians of Argentina.'' Monitore Zoologica Italiano, New Series Monografia, Firenze, 2, 1-609.

Cerezoli, J. P. M. (2008). Anurofauna em Riachos de Fragmentos Florestais da Chapada das Perdizes, Serra de Carrancas, sul de Minas Gerais. Universidade Federal de Lavras, Lavras-MG.

Cisneros-Heredia, D. F., and McDiarmid, R. W. (2007). ''Revision of the characters of Centrolenidae (Amphibia: Anura: Athesphatanura), with comments on its taxonomy and the description of new taxa of glassfrogs.'' Zootaxa, 1572, 1-82.

Eterovick, P. C., Carnaval, A. C. O. Q., Borges-Nojosa, D. M., Silvano, D. L., Segalla, M. V., and Sazima, I. (2005). ''Amphibian declines in Brazil: an overview.'' Biotropica, 37(2), 166-179.

Haddad, C. F. B., Giovanelli, J. G. R., Giasson, L. O. M., and Toledo, L. F. (2005). Guia sonoro dos anfíbios anuros da Mata Atlântica (Sound guide of the Atlantic rain forest anurans). Audio CD. NovoDisc Mídia Digital da Amazônia, Manaus.

Haddad, C. F. B., and Prado, C. P. A. (2005). ''Reproductive modes in frogs and their unexpected diversity in the Atlantic Forest of Brazil.'' BioScience, 55, 207-217.

Hartmann, M.T., Giasson, L.O.M., Hartmann, P. A. and Haddad, C.F.B. (2005). ''Visual communication in Brazilian species of anurans.'' Journal of Natural History, 39(19), 1675–1685.

Heyer, W. R. (1985). ''Taxonomic and natural history notes on frogs of the genus Centrolenella (Amphibia: Centrolenidae) from southeastern Brasil and adjacent Argentina.'' Papeis Avulsos de Zoologia, 36, 1-21.

Heyer, W. R., Rand, A. S., Cruz, C. A. G., Peixoto, O. L., and Nelson, C. E. (1990). ''Frogs of Boracéia.'' Arquivos de Zoologia Sao Paulo, 31, 231-410.

Izecksohn, E., and Carvalho-e-Silva, S. P. (2001). Anfí­bios do Municí­pio do Rio de Janeiro. Editora UFRJ, Rio de Janeiro.

Lucas, E.M. and Fortes, V.B. (2008). ''Frog diversity in the Floresta Nacional de Chapecó, Atlantic Forest of southern Brazil.'' Biota Neotropica, 8(3), 51-61.

Ruiz-Carranza, P.M. and Lynch, J.D. (1991). ''Ranas Centrolenidae de Colombia I: Propuesta de una nueva clasificación genérica.'' Lozanía, (57), 1-30.

Taylor, E.H., and Cochran, D.M. (1953). ''Frogs of the family Centrolenidae from Brasil.'' The University of Kansas Science Bulletin, 35, 1625-1656.

Written by Diogo Borges Provete (dbprovete AT, Department of Zoology and Botany, Universidade Estadual Paulista, campus S�o Jos� do Rio Preto-SP, Brasil
First submitted 2009-01-10
Edited by Keith Lui (2010-05-16)

Species Account Citation: AmphibiaWeb 2010 Vitreorana uranoscopa: Humboldt�s Glass Frog <> University of California, Berkeley, CA, USA. Accessed Apr 24, 2017.

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Citation: AmphibiaWeb. 2017. <> University of California, Berkeley, CA, USA. Accessed 24 Apr 2017.

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