Harlequin Frog, Clown Frog
© 2017 Gonçalo M. Rosa (1 of 21)
Distribution and Habitat
Country distribution from AmphibiaWeb's database: Colombia, Costa Rica, Panama
Life History, Abundance, Activity, and Special Behaviors
Males begin calling and defending territories at the onset of the wet season, and pairing begins 2 to 5 months later, from mid-August through early December (Pounds and Crump 1987; Crump 1988). The sex ratio is male-biased, and males often enter into amplexus early and remain with the female for as long as 32 days (Crump 1988). Females deposit eggs in the water from the end of the wet season to the early dry season, October to December (Pounds and Crump 1987).
Crump (1988) has documented the aggressive behavior of A. varius, which occurs within and between the sexes and is characterized by forelimb and foot wagging, chasing, pouncing, and squashing. Male-male antagonism is generally longer than female-female aggression and involves chirp-like advertisement calls and wrestling behavior. Male aggression is heightened both during the breeding season and in high density situations (Crump 1988). Female-female aggression lacks wrestling and calling, is generally less intense and less frequent, and seems to be related to the defense of foraging and/or shelter sites (Crump 1988). Intersexual aggression is almost always female to male; females will chase, pounce on, and squash males who have invaded their territory, and they will attack males whom they have dislodged from amplexus. The only hostile behavior of males towards females is holding the amplectant position despite a female's efforts to disengage. In a series of invasion experiments, Crump (1988) demonstrated that territorial residents have the advantage in combat and higher success despite size differences.
Trends and Threats
Several causal explanations for this disappearance have been proposed, most involving climatic factors in a direct or synergistic manner. Pounds and Crump (1994) examined weather data and noted the correlation between the adults' disappearance and the 1982-1983 and the 1986-1987 El Niño/Southern Oscillation events. This led them to hypothesize several climate-based causes of the decline: moisture stress, temperature stress, a climate-linked epidemic, and a climate-linked contaminant pulse. Recent studies have linked this and other declines to more subtle but cumulative weather changes caused by global warming. Pounds et al. (1999) conducted a careful analysis of precipitation, air temperature, sea surface temperature, and stream flow patterns as they related to tropical anuran, avian, and anoline lizard communities. They concluded that declines like that of the Harlequin Frog were not simply an effect of the El Niño/Southern Oscillation, but rather of a long-term warming trend which crossed a threshold in late 1980's and precipitated a broad tropical anuran decline. This decline was accompanied by a decline in anoline lizard communities and significant restructuring of tropical avian communities.
Of the proposed causes, the climate-linked epidemic hypothesis (Pounds and Crump 1994) appears particularly important in the decline of A. varius in light of the discovery of the parasitic fly N. bufonivora in 1982 (Crump and Pounds 1985; Pounds and Crump 1987). The fly seems to cause density-dependent mortality (Crump and Pounds 1985), as clumping of frogs during the dry season of 1982 (an El Niño year) was correlated with increased fly parasitism. Parasitism is particularly intense near waterfall spray zones, where Harlequin Frogs aggregate when extreme dry conditions threaten their water balance (Pounds and Crump 1987).
An additional epidemic and density-dependent threat to A. varius has appeared in the form of a novel pathogen. In 1997, Berger et al (1998) documented three deceased A. varius specimens from Fortuna, Panama which had been killed by a chytridiomycete fungus. This fungal pathogen invades keratinized body surfaces and kills postmetamorphic anurans within several weeks. Tests show that the chytrid fungus can be spread by skin scrapings from other individuals, and may impair cutaneous respiration and osmoregulation when it attacks the hypervascularized pelvic patch (Berger et al 1998). It has been documented as fatal in adults from 18 other species, both in South America and Australia, and has been implicated as a widespread cause of anuran decline (Berger et al 1998).
Possible reasons for amphibian decline
Subtle changes to necessary specialized habitat
A Spanish-language species account can be found at the website of Instituto Nacional de Biodiversidad (INBio).
Berger, L., Speare, R., Daszak, P., Green, D. E., Cunningham, A. A., Goggin, C. L., Slocombe, R., Ragan, M. A., Hyatt, A. D., McDonald, K. R., Hines, H. B., Lips, K. R., Marantelli, G., and Parkes, H. (1998). "Chytridiomycosis causes amphibian mortality associated with population declines in the rain forests of Australia and Central America." Proceedings of the National Academy of Sciences of the United States of America, 95(15), 9031-9036.
Crump, M. L., and Pounds, J. A. (1985). ''Lethal parasitism of an aposematic anuran (Atelopus varius) by Notochaeta bufonivora (Diptera: Sarcophagidae).'' Journal of Parasitology, 71(5), 588-591.
Crump, M.L. (1988). ''Aggression in Harlequin Frogs: male-male competition and a possible conflict of interest between the sexes.'' Animal Behaviour, 36(4), 1064-1077.
Daly, J.W., Padgett, W.L., Saunders, R.L., and Cover, J.F., Jr. (1997). ''Absence of tetrodotoxins in a captive-raised riparian frog, Atelopus varius.'' Toxicon, 35(5), 705-709.
Holdridge, L. R. (1967). Life Zone Ecology. Tropical Science Center, San Jose, Costa Rica.
Pounds, J. A., Fogden, M. P. L., and Campbell, J. H. (1999). ''Biological response to climate change on a tropical mountain.'' Nature, 398(6728), 611-615.
Pounds, J. A., and Crump, M. L. (1987). ''Harlequin Frogs along a tropical montane stream: Aggregation and the risk of predation by frog-eating flies.'' Biotropica, 19(4), 306-309.
Pounds, J. A., and Crump, M. L. (1989). ''Temporal variation in the dispersion of a tropical anuran.'' Copeia, 1989(1), 209-211.
Pounds, J. A., and Crump, M. L. (1994). ''Amphibian declines and climate disturbance: The case of the Golden Toad and the Harlequin Frog.'' Conservation Biology, 8(1), 72-85.
Savage, J.M. (1972). ''The harlequin frogs, genus Atelopus, of Costa Rica and western Panama.'' Herpetologica, 28(2), 77-94.
Written by Sean Schoville (sschov AT uclink4.berkeley.edu), MVZ University of California at Berkeley
First submitted 1999-10-22
Edited by Duncan Parks and Meredith J. Mahoney, Tate Tunstall 2004 update (2009-11-02)
Species Account Citation: AmphibiaWeb 2009 Atelopus varius: Harlequin Frog <http://amphibiaweb.org/species/88> University of California, Berkeley, CA, USA. Accessed Nov 25, 2020.
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Citation: AmphibiaWeb. 2020. <http://amphibiaweb.org> University of California, Berkeley, CA, USA. Accessed 25 Nov 2020.
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