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Whitfield Et Al 2012
BIOTROPICA 0(0): 1–6 2012

10.1111/j.1744-7429.2012.00872.x

Temporal Variation in Infection Prevalence by the Amphibian Chytrid Fungus in Three
Species of Frogs at La Selva, Costa Rica
Steven M. Whitfield2,4, Jacob Kerby2, Lydia R. Gentry3, and Maureen A. Donnelly1
1

Department of Biological Sciences, Florida International University, UP Campus, OE 167, Miami, Florida, U.S.A.

2

Biology Department, University of South Dakota, Vermillion, South Dakota, U.S.A.

3

College of Veterinary Medicine, Washington State University, Pullman, Washington, U.S.A.

ABSTRACT
The emerging infectious disease chytridiomycosis, caused by the amphibian chytrid fungus, Batrachochytrium dendrobatidis (Bd), is implicated in widespread population declines, extirpations, and extinctions of amphibians throughout the world. In the Neotropics, most amphibian declines have occurred in cool mid- to high-elevation sites (> 400 m asl), and it is hypothesized that high temperatures limit the growth of Bd in lowland tropical sites, despite few data available on the distribution of Bd in lowland forests. Here, we report the results of a
12-mo pathogen surveillance program for three common species of frogs at a warm lowland site in northeastern Costa Rica. We combine standard non-invasive skin swabbing techniques with a quantitative polymerase chain reaction assay to analyze the infection prevalence and Bd load across a 1-yr period. Our data indicate an overall Bd infection rate of 6.1 percent, but prevalence varies from < 5 percent in warmer months to a peak of 34.7 percent in the coolest months of the year. Despite very little seasonal variation in temperature (< 4°C), our data indicate strong seasonal variation in the prevalence of Bd, with highest prevalence of infection in months with coolest air temperatures. While it has been suggested that Bd is primarily a riparian fungus, we find no difference in prevalence of infection among our species despite considerable differences in affiliation of



Cited: MAHONY, N. SHEPPARD, C. WILLIAMS, AND M. J. TYLER. 2004. Effect of season and temperature on mortality in amphibians due to chytridiomycosis BREM, F. M. R., AND K. R. LIPS. 2008. Batrachochytrium dendrobatidis infection patterns among Panamanian amphibian species, habitats and elevations BUTTERFIELD, R. P. 1994. The regional context: Land colonization and conservation in Sarapiqui. In L. A. McDade, K. S. Bawa, H. A. Hespenheide, and G. S. Hartshorn (Eds.). La Selva: Ecology and natural history of a neotropical rain forest, pp CLARK, D. B. 1990. La Selva Biological Station: A blueprint for stimulating tropical research CLARK, D. A., S. C. PIPER, C. D. KEELING, AND D. B. CLARK. 2003. Tropical rain forest tree growth and atmospheric carbon dynamics linked to COLWELL, R. K., G. BREHM, C. L. CARDELUS, A. C. GILMAN, AND J. T. LONGINO. 2008. Global warming, elevational range shifts, and lowland biotic attrition in the wet tropics DONNELLY, M. A. 1989. Reproductive phenology and age structure of Dendrobates pumilio in northeastern Costa Rica. J. Herpetology, 23: 362–367. DONNELLY, M. A. 1999. Reproductive phenology of Eleutherodactylus bransfordii in northeastern Costa Rica J. A. PEREZ, AND T. GARLAND. 2009. Why tropical forest lizards are vulnerable to climate warming MARANTELLI, F. FLEASON, AND A. COLLING. 2007. Diagnostic assays and sampling protocols for the detection of Batrachochytrium dendrobatidis JOHNSON, M. L., L. BERGER, L. PHILIPS, AND R. SPEARE. 2003. Fungicidal effects of chemical disinfectants, UV light, desiccation and heat on the KRIGER, K. M., AND J. M. HERO. 2006. Survivorship in wild frogs infected with chytridiomycosis KRIGER, K. M., AND J.-M. HERO. 2007a. Large-scale seasonal variation in the prevalence and severity of chytridiomycosis KRIGER, K. M., AND J. M. HERO. 2007b. The chytrid fungus Batrachochytrium dendrobatidis is non-randomly distributed across amphibian breeding KRIGER, K. M., AND J. M. HERO. 2008. Altitudinal distribution of chytrid (Batrachochytrium dendrobatidis) infection in subtropical Australian frogs. LIEBERMAN, S. S. 1986. Ecology of the leaf litter herpetofauna of a neotropical rain forest: La Selva, Costa Rica LIPS, K. R., F. BREM, R. BRENES, J. D. REEVE, R. A. ALFORD, J. VOYLES, C. CAREY, L. LIVO, A. P. PESSIER, AND J. P. COLLINS. 2006. Emerging infectious disease and the loss of biodiversity in a Neotropical amphibian community LIPS, K. R., J. DIFFENDORFER, J. R. MENDELSON, AND M. W. SEARS. 2008. Riding the wave: Reconciling the roles of disease and climate change in amphibian declines LIPS, K. R., J. D. REEVE, AND L. R. WITTERS. 2003. Ecological traits predicting amphibian population declines in Central America LONGO, A. V., P. A. BURROWES, AND R. L. JOGLAR. 2010. Seasonality of Batrachochytrium dendrobatidis infection in direct-developing frogs suggests a mechanism for persistence MURRAY, K. A., L. F. SKERRATT, R. SPEARE, AND H. MCCALLUM. 2009. Impact and dynamics of disease in species threatened by the amphibian chytrid fungus, Batrachochytrium dendrobatidis HOSSACK, B. A. LAMBERT, R. MCCAFFERY, AND C. GAUGHAN. 2010. PIOTROWSKI, J. S., S. L. ANNIS, AND J. E. LONGCORE. 2004. Physiology of Batrachochytrium dendrobatidis, a chytrid pathogen of amphibians. Mycologia 96: 9–15. PUSCHENDORF, R., F. BOLANOS, AND G. CHAVES. 2006. The amphibian chytrid fungus along an altitudinal transect before the first reported declines RICHARDS-ZAWACKI, C. L. 2010. Thermoregulatory behaviour affects prevalence of chytrid fungal infection in a wild population of Panamanian golden frogs

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