Revista de Biología Tropical ISSN Impreso: 0034-7744 ISSN electrónico: 2215-2075

OAI: https://revistas.ucr.ac.cr/index.php/rbt/oai
Amphibians and reptiles in the swamps dominated by the palm Raphia taedigera (Arecaceae) in northeastern Costa Rica.
PDF (Español (España))

Keywords

Raphia taedigera
palm wetland
rainforest herpetofauna
Tortuguero
La Selva.
Raphia taedigera
Manicaria saccifera
pantanos dominados por plamas
herpetofauna de bosque húmedo tropical
Tortuguero
Estación Biológica La Selva.

How to Cite

Bonilla-Murillo, F., Beneyto, D., & Sasa, M. (2013). Amphibians and reptiles in the swamps dominated by the palm Raphia taedigera (Arecaceae) in northeastern Costa Rica. Revista De Biología Tropical, 61(S1), 143–161. https://doi.org/10.15517/rbt.v61i1.23185

Abstract

The herpetofauna that inhabits Caribbean Costa Rica has received considerable attention in the last two decades. This assemblage includes a total of 141 species of reptiles and 95 amphibians mostly distributed in tropical wet and moist lowland forests. While most information available came from primary and secondary forest sites, little is known about the amphibians and reptiles that inhabit more open habitats, such as wetlands and swamps. For instances, swaps dominated by the yolillo palm Raphia taedigera extend through much of the northeastern Caribbean coast of Costa Rica and eastern Nicaragua, but information about the herpetological community that uses such environments remains practically unknown. This situation reflects the little research conducted in such inhospitable environments. Here, we report the results of an intensive survey conducted to assess the herpetological community that inhabit R. taedigera palm-swamps. A total of 14 species of amphibians and 17 of reptiles have been recorded from these swamps. Amphibians and reptiles that inhabit yolillo swamps have wide distributions along much of Middle America and are considered common species throughout their range. In general, yolillo swamps are poor environments for herpetofauna: richness of reptiles and amphibians is almost two times higher in the adjacent forest than in the palm dominated swamps. Furthermore, most species observed in this swamps can be considered habitat generalists that are well adapted to the extreme conditions imposed by the changes in hydroperiods, reduce understory cover, low tree diversity and simple forest architecture of these environments. Despite similarities in the herpetofauna, it is clear that not all forest species use yolillo habitat, a characteristic that is discussed in terms of physical stress driven by the prolonged hydroperiod and reduced leaflitter in the ground, as these features drive habitat structure and herpetofaunal complexity. Our list of species using yolillo swamps is not definitive, and is likely to grow as more studies are conducted in this unexplored environment.

 
https://doi.org/10.15517/rbt.v61i1.23185
PDF (Español (España))

References

Beneyto, D., J.S. Monrós & R. Piculo. 2013. Los yolillales como fuentes o sumideros de ornitofauna: una primera aproximación al problema. Rev. Biol. Trop. 61 (Supl. 1): 131-142.

Burger, R.M. 2001. The herpetofauna of Caño Palma Biological Station, Tortuguero, Costa Rica. Bull. Chicago Herp. Soc. 36: 243-253.

Calvo-Gutiérrez, C.M., F. Bonilla-Murillo & M. Sasa. 2013. Uso y conservación de humedales de yolillo Raphia taedigera (Arecaceae) en el Área de Conservación Tortuguero, Costa Rica. Rev. Biol. Trop. 61 (Supl. 1): 163-178.

Carrillo, E., J. Saenz & K. Todd. 1992. Fuller movements and activities of white-lipped peccaries in Corcovado National Park, Costa Rica. Biol. Cons. 108: 317-324.

Castoe, T.A., J.M. Daza, E.N. Smith, M. Sasa, U. Kuch, J.A. Campbell, P.T. Chippindale & C.L. Pakinson. 2009. Comparative phylogeography of pitvipers suggest a consensus of ancient Middle American highland biogeography. J. Biogeogr.36: 88-103.

Crump, M.L. & N.J. Scott Jr. 1994. Visual encounter surveys, p. 84-92. In R.W. Heyer, M.A. Donnelly, R.W. McDiarmid, L.C. Hayek & M.S Foster (eds.). Measuring and monitoring biological diversity. Standard methods for amphibians. Smithsonian, Barro Colorado Island, Panama.

Duellman, W.E. 1966. The Central American herpetofauna: an ecological perspective. Copeia: 700-719.

Duellman, W. E. & L. Trueb. 1994. Biology of Amphibians. The John Hopkins University, Baltimore, EE.UU.

Gillespie, G.R. 2002. Impacts of sediment loads, tadpole density, and food type on the growth and development of tadpoles of the spotted tree frog Litoria spenceri: an in-stream experiment. Biol. Cons. 106: 141-150.

Gotelli, N.J. & G.L. Entsminger. 2001. EcoSim: Null models software for ecology. Version 7.0. Acquired Intelligence Inc. & Kesey-Bear. Consultado: 30 julio 2012, www.homepages.together.net/~gentsmin/ecosim.htm

Guyer, C. 1994. The reptile fauna: diversity and ecology, p. 210-216. In L.A. McDade, K.S. Bawa, H.A. Hespenheide & G.S. Harstshorn (eds.). La Selva: ecology and natural history of a neotropical rainforest. University of Chicago, Chicago, Illinois, EE.UU.

Guyer, C. & M.A. Donnelly. 2005. Amphibians and reptiles of La Selva, Costa Rica, and the Caribbean slope: a comprehensive guide. University of California, Berkeley, California, EE.UU.

Holdridge, L.R. 1967. Life zone ecology. Tropical Science Center, San José, Costa Rica.

McCormick, S. & G.A. Polis. 1982. Invertebrate that preys on vertebrates. Biol. Rev. 57: 29-58.

Menin, M., D.J. Rodrigues & C.S. de Azevedo. 2005. Predation on amphibians by spiders (Arachnida, Araneae) in the neotropical region. Phyllomedusa 4: 39-47.

Moreno, C.E. 2001. Métodos para medir la biodiversidad. M&T–Manuales y Tesis SEA, vol. 1. Zaragoza, España.

Myers, R.L. 1981. The ecology of low diversity palm swamps near Tortuguero, Costa Rica. Ph.D. thesis, University of Florida, Gainesville, Florida, EE.UU.

Myers, R.L. 2013a. Humedales dominados por palmas (Arecaceae), con énfasis en aquellos distribuidos en Costa Rica y Nicaragua. Rev. Biol. Trop. 61 (Supl. 1): 5-24.

Myers, R.L. 2013b. Fenología y crecimiento de Raphia taedigera (Aracaceae) en humedales del noreste de Costa Rica. Rev. Biol. Trop. 61 (Supl. 1): 35-45.

Myers, R.L. 2013c. Producción de hojarasca y descomposición en humedales dominados por palmas (Aracaceae) en el noreste de Costa Rica. Rev. Biol. Trop. 61 (Supl. 1): 87-99.

Pielou, E.C. 1975. Ecological diversity. Wiley, Nueva York, EE.UU.

Rueda, R., O. Jarquin, B. Munguia, A. Reyes & I. Coronado. 2012. Rev. Biol. Trop. 61 (Supl. 1): 101-120.

Savage, J.M. 2002. The amphibians and reptiles of Costa Rica: a herpetofauna between two continents, between two seas. University of Chicago, Chicago, Illinois, EE.UU.

Sanders, H. 1968. Marine benthic diversity: a comparative study. The Am. Nat. 102: 243-282.

Sasa, M., D. Wasko & W.W. Lamar. 2009. Natural history of the terciopelo Bothrops asper in Costa Rica. Toxicon 54: 904-922.

Sasa, M., G. Chaves & L.W. Porras. 2010. The Costa Rican herpetofauna: conservation status and future perspectives, p. 509-603. In L.D. Wilson, J.H. Townsend & J.D. Johnson (eds.). Conservation of Mesoamerican Amphibians and Reptiles. Eagle Mountain, Utah, EE.UU.

Serrano, J., F. Bonilla-Murillo & M. Sasa. 2013. Distribución, superficie y área protegida de humedales dominados por palmas (Arecaceae) en Costa Rica y Nicaragua. Rev. Biol. Trop. 61 (Supl. 1): 25-33.

Webb, S.D. 1991. Ecogeography and the Great American Interchange. Paleobiology 17: 266-280.

Wilson, L.D. & J.D. Johnson. 2010. Distributional patterns of the herpetofauna of Mesoamerica, a biodiversity hotspot, p. 31-235. In L.D. Wilson, J.H. Townsend & J.D. Johnson (eds.). Conservation of Mesoamerican Amphibians and Reptiles. Eagle Mountain, Utah, EE.UU.

Wood, S.L.R. & J.S. Richardson. 2009. Impact of sediment and nutrient inputs on growth and survival of tadpoles of the Western Toad. Freshwat. Biol. 54: 1120-1134.

Comments

Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 International License.

Copyright (c) 2013 Revista de Biología Tropical

Downloads

Download data is not yet available.