Sexual maturity and sexual dimorphism in a population of the rocket-frog Colostethus aff. fraterdanieli (Anura: Dendrobatidae) on the northeastern Cordillera Central of Colombia

Authors

  • Yeison Tolosa Universidad de Antioquia
  • Claudia Molina-Zuluaga Universidad de Antioquia
  • Adriana Restrepo Universidad de Antioquia https://orcid.org/0000-0003-3895-8014
  • Juan M. Daza Universidad de Antioquia

DOI:

https://doi.org/10.17533/udea.acbi.329007

Keywords:

Andes, anfibios, gónadas, histología, morfometría, reproducción

Abstract

The minimum size of sexual maturity and sexual dimorphism are important life history traits useful to study and understand the population dynamics of any species. In this study, we determined the minimum size at sexual maturity and the existence of sexual dimorphism in a population of the rocket-frog, Colostethus aff. fraterdanieli, by means of morphological and morphometric data and macro and microscopic observation of the gonads. Females attained sexual maturity at 17.90 ± 0.1 mm snout-vent length (SVL), while males attained sexual maturity at 16.13 ± 0.06 mm SVL. Females differed from males in size, shape and throat coloration. Males were smaller than females and had a marked and dark throat coloration that sometimes extended to the chest, while females lacked this characteristic, with a throat either immaculate or weakly pigmented. In this study, we describe some important aspects of the reproductive ecology of a population of C. aff. fraterdanieli useful as a baseline for other more specialized studies.

|Abstract
= 520 veces | PDF (ESPAÑOL (ESPAÑA))
= 140 veces| | HTML (ESPAÑOL (ESPAÑA))
= 34 veces|

Downloads

Download data is not yet available.

Author Biographies

Yeison Tolosa, Universidad de Antioquia

Grupo Herpetológico de Antioquia, Instituto de Biología, Universidad de Antioquia, AA 1226, Medellín, Colombia.

Claudia Molina-Zuluaga, Universidad de Antioquia

Grupo Herpetológico de Antioquia, Instituto de Biología, Universidad de Antioquia, AA 1226, Medellín, Colombia.

Adriana Restrepo, Universidad de Antioquia

Grupo Herpetológico de Antioquia, Instituto de Biología, Universidad de Antioquia, AA 1226, Medellín, Colombia.

Juan M. Daza, Universidad de Antioquia

Grupo Herpetológico de Antioquia, Instituto de Biología, Universidad de Antioquia, AA 1226, Medellín, Colombia.

References

Bailey LL, Simons TR, Pollock KH. 2004. Spatial and temporal variation in detection probability of Plethodon salamanders using the robust capture-recapture design. Journal of Wildlife Management, 68: 14-24.

Bourne GR, Collins AC, Holder AM, McCarthy CL. 2001. Vocal communication and reproductive behavior of the frog Colostethus beebei in Guyana. Journal of Herpetology, 35: 272-281.

Buchanan BW. 1994. Sexual dimorphism in Hyla squirella: Chromatic and pattern variation between the sexes. Copeia, 1994: 797-802.

Crump M, Scott NJ. 2001. Relevamientos por encuentros visuales. In: Heyer R, Donnelly MD, McDiarmid LA, Hayek A, Foster MS. editors. Medición y monitoreo de la diversidad biológica. Métodos estandarizados para anfibios. Comodoro Rivadavia (Argentina): Editorial Universitaria de la Patagonia. p. 80-87.

Cummins CP, Swan MJ. 1995. Variation in reproductive characteristics of the stream frog Colostethus trinitatis on the island of Trinidad. Journal of Tropical Ecology, 11: 603-618.

Dixon JR, Rivero-Blanco C. 1985. A new dendrobatid frog (Colostethus) from Venezuela with notes on its natural history and that of related species. Journal of Herpetology, 19: 177-184.

Duellman W, Trueb L.1994. Biology of amphibians. Baltimore and London: The Johns Hopkins University Press. p. 670.

Fandiño MC, Lüddecke H, Amézquita A. 1997. Vocalisation and larval transportation of male Colostethus subpunctatus (Anura: Dendrobatidae). Amphibia-Reptilia, 18: 39-48.

Felgueiras-Napoli M. 2005. A new species allied to Hyla circumdata (Anura: Hylidae) from Serra da Mantiqueira, Southeastern Brazil. Herpetologica, 61: 63-69.

Grant T. 2004. On the identities of Colostethus inguinalis (Cope, 1868) and C. panamensis (Dunn, 1933), with comments on C. latinasus (Cope, 1863) (Anura: Dendrobatidae). American Museum Novitates, 3444: 1-24.

Grant T, Castro F. 1998. The cloud forest Colostethus (Anura, Dendrobatidae) of region of the Cordillera Occidental of Colombia. Journal of Herpetology, 32: 378-392.

Grant T, Frost DR, Caldwell JP, Gagliardo R, Haddad CF, Kok PJ, Means DB, Noonan BP, Schargel WE, Wheeler WC. 2006. Phylogenetic systematics of dart-poison frogs and their relatives (Amphibia: Athesphatanura: Dendrobatidae). Bulletin of the American Museum of Natural History, 299: 1-262.

Greenberg B. 1942. Some effects of testosterone in the sexual pigmentation and other sex characters of the cricket frog (Acris gryllus). Journal of Experimental Zoology, 91: 435-446.

Hammer O, Harper DAT, Ryan PD. 2001. Past: paleontological statistics software package for education and data analysis. Palaentologia Electronica, 4: 9.

Holdridge LR. 2000. Ecología basada en zonas de vida. Quinta reimpresión. San José (Costa Rica): Instituto Interamericano de Cooperación para la Agricultura (IICA). p. 216.

Howard RD. 1978. The influence of male-defended oviposition sites on early embryo mortality in bullfrogs. Ecology, 59: 789-798.

Howard RD. 1981. Sexual dimorphism in bullfrogs. Ecology, 62: 303-310.

Juncá FA. 1998. Reproductive biology of Colostethus stepheni and Colostethus marchesianus (Dendrobatidae), with the description of a new anuran mating behavior. Herpetologica, 54: 377-387.

Katsikaros K, Shine R. 1997. Sexual dimorphism in the tusked frog, Adelotus brevis (Anura: Myobatrachidae): the role of natural and sexual selection. Biological Journal of the Linnean Society, 60: 39-51.

Krzanowski WJ. 1979. Between groups comparison of principal components. Journal of the American Statistical Association, 74: 703-707.

Lima AP, Keller C. 2003. Reproductive characteristics of Colostethus marchesianus from its type locality in Amazonas, Brazil. Journal of Herpetology, 37: 754-757.

Lima AP, Caldwell JP, Biavati GM. 2002. Territorial and reproductive behavior of an Amazonian dendrobatid frog, Colostethus caeruleodactylus. Copeia, 2002: 44-51.

Lovich JE, Gibbons JW. 1992. A review of techniques for quantifying sexual size dimorphism. Growth, Development, & Aging, 56: 269-281.

Lovich JE, Gibbons JW, Agha M. 2014. Does the timing of attainment of maturity influence sexual size dimorphism and adult sex ratio in turtles? Biological Journal of the Linnean Society, 112: 142-149.

Luna L. 1968. Manual of Histologic Staining Methods of the Armed Forces Institute of Pathology. Third edition. New York (U. S. A.): Blakiston division, McGraw-Hill. p. 258.

Lynch JD. 1996. Eleutherodactylus erythropleura. Catalogue of American Amphibians and Reptiles, 623: 1-3.

Mazerolle MJ, Bailey LL, Kendall WL, Andrew-Royle J, Converse SJ, Nichols JD. 2007. Making great leaps forward: accounting for detectability in herpetological field studies. Journal of Herpetology, 41: 672-689.

Méndez-de la Cruz FR, Villagrán-Santa Cruz M, López-Ortíz ML, Hernández-Gallegos O. 2013. Reproductive cycle of a high- elevation, oviparous lizard (Sceloporus spinosus: Reptilia: Phrynosomatidae). The Southwestern Naturalist, 58: 54-63.

Morrison C, Hero J-M. 2003. Geographic variation in life-history characteristics of amphibians: A review. Journal of Animal Ecology, 72: 270-279.

Morrison C, Hero J-M, Browning J. 2004. Altitudinal variation in the age at maturity, longevity and reproductive lifespan of anurans in subtropical Queensland. Herpetologica, 60: 34-44.

Prado A, Abdalla F, Silva P, Zina J. 2004. Late gametogenesis in Leptodactylus labyrinthicus (Amphibia, Anura, Leptodactylidae) and some ecological considerations. Brazilian Journal of Morphological Sciences, 21: 177-184.

Reyment RA, Blackith RE, Campell NA. 1984. Multivariate morphometrics. Second edition. Michigan (U. S. A.): Academic Press. p. 233.

Rojas B, Endler JA. 2013. Sexual dimorphism and intra-populational color pattern variation in the aposematic frog Dendrobates tinctorius. Evolutionary Ecology, 27: 739-753.

Roff DA. 1992. The evolution of life histories: Theory and analysis. New York, (U. S. A.): Chapman & Hall. p. 527.

Roff DA. 2000. Trade-offs between growth and reproduction: an analysis of the quantitative genetic evidence. Journal of Evolutionary Biology, 13: 434-445.

Rueda-Almonacid JV, Lynch JD. 1983. Una nueva especie de Eleutherodactylus para la cordillera oriental de Colombia. Lozania, 42: 1-6.

Shine R. 1979. Sexual selection and sexual dimorphism in the Amphibia. Copeia, 1979: 297-306.

Shine R. 1989. Ecological causes for the evolution of sexual dimorphism: A review of the evidence. The Quarterly Review of Biology, 64: 419-461.

de Solla SR, Shirose LJ, Fernie KJ, Barrett GC, Brousseau CS, Bishop, CA. 2005. Effect of sampling effort and species detectability on volunteer based anuran monitoring programs. Biological Conservation, 121: 585-594.

Stearns SC. 1992. The evolution of life histories. New York (U. S. A.): Oxford University Press. p. 246.

Wake MH, Dickie R. 1998. Oviduct structure, function, and reproductive modes in amphibians. The Journal of Experimental Zoology, 282: 477-506.

Watling J, Donnelly M. 2002. Seasonal patterns of reproduction and abundance of leaf litter frogs in a Central American rainforest. Journal of Zoology, 258: 269-276.

Wells KD. 1978. Territoriality in the green frog (Rana clamitans): vocalizations and agonistic behavior. Animal Behaviour, 26: 1051-1063.

Wells KD. 1980. Behavioral ecology and social organization of a dendrobatid frog (Colostethus inguinalis). Behavioral Ecology and Sociobiology, 6: 199-209.

Woolbright LL. 1983. Sexual selection and size dimorphism in anuran amphibian. The American Naturalist, 121: 110-119.

Yezerinac SM, Lougheed SC, Handford P. 1992. Measurement error and morphometric studies. Systematic Biology, 41: 471-482.

Published

2017-10-02

How to Cite

Tolosa, Y., Molina-Zuluaga, C., Restrepo, A., & Daza, J. M. (2017). Sexual maturity and sexual dimorphism in a population of the rocket-frog <i>Colostethus</i> aff. <i>fraterdanieli</i> (Anura: Dendrobatidae) on the northeastern Cordillera Central of Colombia. Actualidades Biológicas, 37(102), 47–54. https://doi.org/10.17533/udea.acbi.329007

Issue

Section

Full articles