Ecophysiology meets conservation: understanding the role of disease in amphibian population declines

Global trends in emerging infectious diseases

Jones, K. E., Patel, N. G., Levy, M. A., Storeygard, A., Balk, D., Gittleman, J. L., & Daszak, P. (2008) · Nature · doi:10.1038/nature06536 · Cited by 8,338 · see citing works

Emerging Infectious Diseases of Wildlife-- Threats to Biodiversity and Human Health

Daszak, P., Cunningham, A. A., & Hyatt, A. D. (2000) · Science · doi:10.1126/science.287.5452.443 · Cited by 4,913 · see citing works

Status and Trends of Amphibian Declines and Extinctions Worldwide

Stuart, S. N., Chanson, J. S., Cox, N. A., Young, B. E., Rodrigues, A. S. L., Fischman, D. L., & Waller, R. W. (2004) · Science · doi:10.1126/science.1103538 · Cited by 4,508 · see citing works

Climate Warming and Disease Risks for Terrestrial and Marine Biota

Harvell, C. D., Mitchell, C. E., Ward, J. R., Altizer, S., Dobson, A. P., Ostfeld, R. S., & Samuel, M. D. (2002) · Science · doi:10.1126/science.1063699 · Cited by 2,729 · see citing works

Climate change and water.

Bates, B. C., Kundzewicz, Z. W., & Wu, S. (2008) · TaCCIRe Repository (Sokoine University of Agriculture) · Cited by 2,641 · see citing works

Superspreading and the effect of individual variation on disease emergence

Lloyd-Smith, J. O., Schreiber, S. J., Kopp, P. E., & Getz, W. M. (2005) · Nature · doi:10.1038/nature04153 · Cited by 2,514 · see citing works

Impacts of biodiversity on the emergence and transmission of infectious diseases

Keesing, F., Belden, L. K., Daszak, P., Dobson, A., Harvell, C. D., Holt, R. D., Hudson, P., Jolles, A., Jones, K. E., Mitchell, C. E., et al. (2010) · Nature · doi:10.1038/nature09575 · Cited by 2,043 · see citing works

Chytridiomycosis causes amphibian mortality associated with population declines in the rain forests of Australia and Central America

Berger, L., Speare, R., Daszak, P., Green, D. E., Cunningham, A. A., Goggin, C. L., Slocombe, R. F., Ragan, M. A., Hyatt, A. D., McDonald, K., et al. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.15.9031 · Cited by 2,011 · see citing works

Widespread amphibian extinctions from epidemic disease driven by global warming

Alan Pounds, J., Bustamante, M. R., Coloma, L. A., Consuegra, J. A., Fogden, M. P. L., Foster, P. N., La Marca, E., Masters, K. L., Merino-Viteri, A., Puschendorf, R., et al. (2006) · Nature · doi:10.1038/nature04246 · Cited by 1,960 · see citing works

Emerging Marine Diseases--Climate Links and Anthropogenic Factors

Harvell, C. D., Kim, K., Burkholder, J. M., Colwell, R. R., Epstein, P. R., Grimes, D. J., Hofmann, E. E., Lipp, E. K., Osterhaus, A. D. M. E., Overstreet, R. M., et al. (1999) · Science · doi:10.1126/science.285.5433.1505 · Cited by 1,836 · see citing works

The anti-inflammatory and immunosuppressive effects of glucocorticoids, recent developments and mechanistic insights

Coutinho, A. E., & Chapman, K. E. (2011) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2010.04.005 · Cited by 1,815 · see citing works

Are we in the midst of the sixth mass extinction? A view from the world of amphibians

Wake, D. B., & Vredenburg, V. T. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0801921105 · Cited by 1,786 · see citing works

Emerging infectious diseases of plants: pathogen pollution, climate change and agrotechnology drivers

Anderson, P. K., Cunningham, A. A., Patel, N., Morales, F. J., Epstein, P. R., & Daszak, P. (2004) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2004.07.021 · Cited by 1,717 · see citing works

The physiology/life-history nexus

Ricklefs, R. E., & Wikelski, M. (2002) · Trends in Ecology & Evolution · doi:10.1016/s0169-5347(02)02578-8 · Cited by 1,597 · see citing works

Effects of species diversity on disease risk

Keesing, F., Holt, R. D., & Ostfeld, R. S. (2006) · Ecology Letters · doi:10.1111/j.1461-0248.2006.00885.x · Cited by 1,563 · see citing works

The use of leukocyte profiles to measure stress in vertebrates: a review for ecologists

Davis, A. K., Maney, D. L., & Maerz, J. C. (2008) · Functional Ecology · doi:10.1111/j.1365-2435.2008.01467.x · Cited by 1,558 · see citing works

Quantitative evidence for global amphibian population declines

Houlahan, J. E., Findlay, C. S., Schmidt, B. R., Meyer, A. H., & Kuzmin, S. L. (2000) · Nature · doi:10.1038/35008052 · Cited by 1,332 · see citing works

Spread of Chytridiomycosis Has Caused the Rapid Global Decline and Extinction of Frogs

Skerratt, L. F., Berger, L., Speare, R., Cashins, S. D., McDonald, K., Phillott, A. D., Hines, H. B., & Kenyon, N. (2007) · EcoHealth · doi:10.1007/s10393-007-0093-5 · Cited by 1,235 · see citing works

Experimental Infection of North American Birds with the New York 1999 Strain of West Nile Virus

Komar, N., Langevin, S., Hinten, S., Nemeth, N., Edwards, E., Hettler, D., Davis, B., Bowen, R., & Bunning, M. (2003) · Emerging Infectious Diseases · doi:10.3201/eid0903.020628 · Cited by 1,216 · see citing works

Batrachochytrium Dendrobatidis gen. et sp. nov., a Chytrid Pathogenic to Amphibians

Longcore, J. E., Pessier, A. P., & Nichols, D. K. (1999) · Mycologia · doi:10.2307/3761366 · Cited by 1,052 · see citing works

Is a healthy ecosystem one that is rich in parasites?

Hudson, P. J., Dobson, A. P., & Lafferty, K. D. (2006) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2006.04.007 · Cited by 989 · see citing works

Emerging Infectious Diseases and Amphibian Population Declines

Daszak, P., Berger, L., Cunningham, A. A., Hyatt, A. D., Green, D. E., & Speare, R. (1999) · Emerging infectious diseases · doi:10.3201/eid0506.990601 · Cited by 985 · see citing works

Climate change and water: technical paper of the intergovernmental panel on climate change

Bates, B. C., Kundzewicz, Z. W., Wu, S., Arnell, N. W., Burgett, V., & Räisänen, J. (2008) · Cited by 953 · see citing works

Identifying Reservoirs of Infection: A Conceptual and Practical Challenge

Haydon, D. T., Cleaveland, S., Taylor, L. H., & Laurenson, M. K. (2002) · Emerging infectious diseases · doi:10.3201/eid0812.010317 · Cited by 879 · see citing works

Decomposing health: tolerance and resistance to parasites in animals

Råberg, L., Graham, A. L., & Read, A. F. (2008) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2008.0184 · Cited by 853 · see citing works

The role of adrenocorticoids as modulators of immune function in health and disease: neural, endocrine and immune interactions

McEwen, B. S., Biron, C. A., Brunson, K. W., Bulloch, K., Chambers, W. H., Dhabhar, F. S., Goldfarb, R. H., Kitson, R. P., Miller, A. H., Spencer, R. L., et al. (1997) · Brain Research Reviews · doi:10.1016/s0165-0173(96)00012-4 · Cited by 837 · see citing works

Infectious disease and amphibian population declines

Daszak, P., Cunningham, A. A., & Hyatt, A. D. (2003) · Diversity and Distributions · doi:10.1046/j.1472-4642.2003.00016.x · Cited by 819 · see citing works

Disentangling Genetic Variation for Resistance and Tolerance to Infectious Diseases in Animals

Råberg, L., Sim, D. G., & Read, A. F. (2007) · Science · doi:10.1126/science.1148526 · Cited by 798 · see citing works

Amphibian Declines: The Conservation Status of United States Species

Lannoo, M. J. (2005) · Project Muse (Johns Hopkins University) · Cited by 795 · see citing works

Immune Defense and Host Life History

Zuk, M., & Stoehr, A. M. (2002) · The American Naturalist · doi:10.1086/342131 · Cited by 773 · see citing works

Physiology of Batrachochytrium dendrobatidis, a Chytrid Pathogen of Amphibians

Piotrowski, J. S., Annis, S. L., & Longcore, J. E. (2004) · Mycologia · doi:10.2307/3761981 · Cited by 753 · see citing works

Complex causes of amphibian population declines

Kiesecker, J. M., Blaustein, A. R., & Belden, L. K. (2001) · Nature · doi:10.1038/35070552 · Cited by 742 · see citing works

Complexity in conservation: lessons from the global decline of amphibian populations

Blaustein, A. R., & Kiesecker, J. M. (2002) · Ecology Letters · doi:10.1046/j.1461-0248.2002.00352.x · Cited by 666 · see citing works

Pathogenesis of Chytridiomycosis, a Cause of Catastrophic Amphibian Declines

Voyles, J., Young, S., Berger, L., Campbell, C. R., Voyles, W. F., Dinudom, A., Cook, D., Webb, R. J., Alford, R. A., Skerratt, L. F., et al. (2009) · Science · doi:10.1126/science.1176765 · Cited by 654 · see citing works

Global Emergence of Batrachochytrium dendrobatidis and Amphibian Chytridiomycosis in Space, Time, and Host

Fisher, M. C., Garner, T. W. J., & Walker, S. F. (2009) · Annual Review of Microbiology · doi:10.1146/annurev.micro.091208.073435 · Cited by 651 · see citing works

Dynamics of an emerging disease drive large-scale amphibian population extinctions

Vredenburg, V. T., Knapp, R. A., Tunstall, T. S., & Briggs, C. J. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0914111107 · Cited by 613 · see citing works

Behavioral endocrinology

(1992) · General and Comparative Endocrinology · doi:10.1016/0016-6480(92)90242-c · Cited by 605 · see citing works

The role of infectious diseases in biological conservation

Smith, K. F., Acevedo‐Whitehouse, K. A., & Pedersen, A. B. (2009) · Animal Conservation · doi:10.1111/j.1469-1795.2008.00228.x · Cited by 561 · see citing works

Pathogen Spillover in Disease Epidemics

Power, A. G., & Mitchell, C. E. (2004) · The American Naturalist · doi:10.1086/424610 · Cited by 555 · see citing works

Skin microbes on frogs prevent morbidity and mortality caused by a lethal skin fungus

Harris, R. N., Brucker, R. M., Walke, J. B., Becker, M. H., Schwantes, C. R., Flaherty, D. C., Lam, B. A., Woodhams, D. C., Briggs, C. J., Vredenburg, V. T., et al. (2009) · The ISME Journal · doi:10.1038/ismej.2009.27 · Cited by 536 · see citing works

Amphibian declines: an immunological perspective

Carey, C., Cohen, N., & Rollins‐Smith, L. A. (1999) · Developmental & Comparative Immunology · doi:10.1016/s0145-305x(99)00028-2 · Cited by 513 · see citing works

Riding the Wave: Reconciling the Roles of Disease and Climate Change in Amphibian Declines

Lips, K. R., Diffendorfer, J. E., MENDELSON, J. R. I., & Sears, M. W. (2008) · PLoS Biology · doi:10.1371/journal.pbio.0060072 · Cited by 510 · see citing works

Enzootic and epizootic dynamics of the chytrid fungal pathogen of amphibians

Briggs, C. J., Knapp, R. A., & Vredenburg, V. T. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0912886107 · Cited by 502 · see citing works

Measuring the Meltdown: Drivers of Global Amphibian Extinction and Decline

Sodhi, N. S., Bickford, D., Diesmos, A. C., Lee, T. M., Koh, L. P., Brook, B. W., Sekercioglu, C. H., & Bradshaw, C. J. A. (2008) · PLoS ONE · doi:10.1371/journal.pone.0001636 · Cited by 492 · see citing works

Neuroendocrinology of the stress-response

Sapolsky, R. (1992) · Medical Entomology and Zoology · Cited by 490 · see citing works

On the evolutionary ecology of specific immune defence

Schmid‐Hempel, P., & Ebert, D. (2003) · Trends in Ecology & Evolution · doi:10.1016/s0169-5347(02)00013-7 · Cited by 488 · see citing works

Agrochemicals increase trematode infections in a declining amphibian species

Rohr, J. R., Schotthoefer, A. M., Raffel, T. R., Carrick, H. J., Halstead, N. T., Hoverman, J. T., Johnson, C. M., Johnson, L. B., Lieske, C. L., Piwoni, M. D., et al. (2008) · Nature · doi:10.1038/nature07281 · Cited by 483 · see citing works

Synergism between trematode infection and pesticide exposure: A link to amphibian limb deformities in nature?

Kiesecker, J. M. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.152098899 · Cited by 461 · see citing works

Global warming and temperature-mediated increases in cercarial emergence in trematode parasites

Poulin, R. (2005) · Parasitology · doi:10.1017/s0031182005008693 · Cited by 452 · see citing works

The ecology and impact of chytridiomycosis: an emerging disease of amphibians

Kilpatrick, A. M., Briggs, C. J., & Daszak, P. (2009) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2009.07.011 · Cited by 434 · see citing works

Direct and Indirect Effects of Climate Change on Amphibian Populations

Blaustein, A. R., Walls, S. C., Bancroft, B. A., Lawler, J. J., Searle, C. L., & Gervasi, S. S. (2010) · Diversity · doi:10.3390/d2020281 · Cited by 428 · see citing works

Predicting climate‐induced range shifts: model differences and model reliability

Lawler, J., White, D., Neilson, R., & Blaustein, A. (2006) · Global Change Biology · doi:10.1111/j.1365-2486.2006.01191.x · Cited by 418 · see citing works

Ecological Traits Predicting Amphibian Population Declines in Central America

Lips, K. R., Reeve, J. D., & Witters, L. R. (2003) · Conservation Biology · doi:10.1046/j.1523-1739.2003.01623.x · Cited by 417 · see citing works

Glucocorticoids and immune function: unknown dimensions and new frontiers.

Wilckens, T., & de Rijk, R. (1997) · Immunology today (Amsterdam. Regular ed.) · doi:10.1016/s0167-5699(97)01111-0 · Cited by 400 · see citing works

Epizootiology of Sixty‐Four Amphibian Morbidity and Mortality Events in the USA, 1996‐2001

Green, D. E., Converse, K. A., & SCHRADER, A. K. (2002) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2002.tb04400.x · Cited by 386 · see citing works

Aquatic eutrophication promotes pathogenic infection in amphibians

Johnson, P. T. J., Chase, J. M., Richgels, K. L. D., Hartson, R. B., Gross, J. A., Larson, D. J., Sutherland, D. R., & Carpenter, S. R. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0707763104 · Cited by 385 · see citing works

The Effect of Trematode Infection on Amphibian Limb Development and Survivorship

Johnson, P. T. J., Lunde, K. B., Ritchie, E. G., & Launer, A. E. (1999) · Science · doi:10.1126/science.284.5415.802 · Cited by 377 · see citing works

Innate immunity and the normal microflora

Boman, H. G. (2000) · Immunological Reviews · doi:10.1034/j.1600-065x.2000.917301.x · Cited by 360 · see citing works

Disease Spread, Susceptibility and Infection Intensity: Vicious Circles?

Beldomenico, P. M., & Begon, M. (2010) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2009.06.015 · Cited by 359 · see citing works

Amphibian Chemical Defense: Antifungal Metabolites of the Microsymbiont Janthinobacterium lividum on the Salamander Plethodon cinereus

Brucker, R. M., Harris, R. N., Schwantes, C. R., Gallaher, T. N., Flaherty, D. C., Lam, B. A., & Minbiole, K. P. C. (2008) · Journal of Chemical Ecology · doi:10.1007/s10886-008-9555-7 · Cited by 357 · see citing works

A Decade of Advances in Iridovirus Research

Williams, T., Barbosa‐Solomieu, V., & Chinchar, V. G. (2005) · Advances in virus research · doi:10.1016/s0065-3527(05)65006-3 · Cited by 345 · see citing works

Putting Theory into Practice: Wildlife Health in Conservation

Deem, S. L., Karesh, W. B., & Weisman, W. (2001) · Conservation Biology · doi:10.1111/j.1523-1739.2001.00336.x · Cited by 339 · see citing works

Ecology and pathology of amphibian ranaviruses

Gray, M., Miller, D. L., & Hoverman, J. T. (2009) · Diseases of Aquatic Organisms · doi:10.3354/dao02138 · Cited by 334 · see citing works

The complexity of amphibian population declines: understanding the role of cofactors in driving amphibian losses

Blaustein, A. R., Han, B. A., Relyea, R. A., Johnson, P. T. J., Buck, J. C., Gervasi, S. S., & Kats, L. B. (2011) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2010.05909.x · Cited by 327 · see citing works

The emerging amphibian pathogen Batrachochytrium dendrobatidis globally infects introduced populations of the North American bullfrog, Rana catesbeiana

Garner, T. W. J., Perkins, M. W., Govindarajulu, P., Seglie, D., Walker, S., Cunningham, A. A., & Fisher, M. C. (2006) · Biology Letters · doi:10.1098/rsbl.2006.0494 · Cited by 327 · see citing works

Infectious Disease Ecology, Effects of Ecosystems in Disease and of Disease on Ecosystems

Schutkowski, H. (2009) · Journal of Archaeological Science · doi:10.1016/j.jas.2009.09.017 · Cited by 326 · see citing works

Amphibian Pathogen Batrachochytrium dendrobatidis Is Inhibited by the Cutaneous Bacteria of Amphibian Species

Harris, R. N., James, T. Y., Lauer, A., Simon, M. A., & Patel, A. C. (2006) · EcoHealth · doi:10.1007/s10393-005-0009-1 · Cited by 324 · see citing works

Experimental evidence that the bullfrog (Rana catesbeiana) is a potential carrier of chytridiomycosis, an emerging fungal disease of amphibians

Daszak, P., Strieby, A., Cunningham, A. A., Longcore, J. E., Brown, C. C., & Porter, D. D. (2004) · Herpetological Journal · Cited by 320 · see citing works

Competition mediated by parasites: biological and theoretical progress

Hudson, P. J. (1998) · Trends in Ecology & Evolution · doi:10.1016/s0169-5347(98)01475-x · Cited by 319 · see citing works

When parasites become prey: ecological and epidemiological significance of eating parasites

Johnson, P. T. J., Dobson, A. P., Lafferty, K. D., Marcogliese, D. J., Memmott, J., Orlofske, S. A., Poulin, R., & Thieltges, D. W. (2010) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2010.01.005 · Cited by 311 · see citing works

ADAPTIVE PLASTICITY IN AMPHIBIAN METAMORPHOSIS: RESPONSE OFSCAPHIOPUS HAMMONDIITADPOLES TO HABITAT DESICCATION

Denver, R. J., Mirhadi, N., & Phillips, M. (1998) · Ecology · doi:10.1890/0012-9658(1998)079[1859:apiamr]2.0.co;2 · Cited by 307 · see citing works

The neuroimmunology of stress from invertebrates to man

Ottaviani, E., & Franceschi, C. (1996) · Progress in Neurobiology · doi:10.1016/0301-0082(95)00049-6 · Cited by 304 · see citing works

Fungicidal effects of chemical disinfectants, UV light, desiccation and heat on the amphibian chytrid Batrachochytrium dendrobatidis

Johnson, M., Berger, L., Philips, L., & Speare, R. (2003) · Diseases of Aquatic Organisms · doi:10.3354/dao057255 · Cited by 304 · see citing works

Metamorphosis and the amphibian immune system

Rollins‐Smith, L. A. (1998) · Immunological Reviews · doi:10.1111/j.1600-065x.1998.tb01265.x · Cited by 303 · see citing works

Confronting Amphibian Declines and Extinctions

MENDELSON, J. R. I., Lips, K. R., Gagliardo, R. W., Rabb, G. B., Collins, J. P., Diffendorfer, J. E., Daszak, P., Roberto Ibáñez, D., Zippel, K. C., Lawson, D. P., et al. (2006) · Science · doi:10.1126/science.1128396 · Cited by 302 · see citing works

Climatic change and wetland desiccation cause amphibian decline in Yellowstone National Park

McMenamin, S. K., Hadly, E. A., & Wright, C. K. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0809090105 · Cited by 296 · see citing works

Co-habiting amphibian species harbor unique skin bacterial communities in wild populations

McKenzie, V. J., Bowers, R. M., Fierer, N., Knight, R. D., & Lauber, C. L. (2011) · The ISME Journal · doi:10.1038/ismej.2011.129 · Cited by 291 · see citing works

Amphibian Decline or Extinction? Current Declines Dwarf Background Extinction Rate

McCallum, M. L. (2007) · Journal of Herpetology · doi:10.1670/0022-1511(2007)41[483:adoecd]2.0.co;2 · Cited by 287 · see citing works

Evaluating the links between climate, disease spread, and amphibian declines

Rohr, J. R., Raffel, T. R., Romansic, J. M., McCallum, H. I., & Hudson, P. J. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0806368105 · Cited by 285 · see citing works

Stress Physiology in Animals.

Balm, P. H. M. (1999) · Cited by 280 · see citing works

WIDESPREAD EFFECTS OF CLIMATIC WARMING ON FRESHWATER ECOSYSTEMS IN NORTH AMERICA

Schindler, D. W. (1997) · Hydrological Processes · doi:10.1002/(sici)1099-1085(19970630)11:8 · Cited by 280 · see citing works

Diseases of Amphibians

Densmore, C. L., & Green, D. E. (2007) · ILAR Journal · doi:10.1093/ilar.48.3.235 · Cited by 278 · see citing works

Chronic stress in free-living European starlings reduces corticosterone concentrations and reproductive success

Cyr, N. E., & Romero, L. M. (2006) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2006.12.003 · Cited by 275 · see citing works

Living fast and dying of infection: host life history drives interspecific variation in infection and disease risk

Johnson, P. T. J., Rohr, J. R., Hoverman, J. T., Kellermanns, E., Bowerman, J., & Lunde, K. B. (2012) · Ecology Letters · doi:10.1111/j.1461-0248.2011.01730.x · Cited by 272 · see citing works

Climate change and outbreaks of amphibian chytridiomycosis in a montane area of Central Spain; is there a link?

Bosch, J., Carrascal, L. M., Durán, L., Walker, S., & Fisher, M. C. (2006) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2006.3713 · Cited by 271 · see citing works

LIFE-HISTORY TRADE-OFFS INFLUENCE DISEASE IN CHANGING CLIMATES: STRATEGIES OF AN AMPHIBIAN PATHOGEN

Woodhams, D. C., Alford, R. A., Briggs, C. J., Johnson, M. L., & Rollins‐Smith, L. A. (2008) · Ecology · doi:10.1890/06-1842.1 · Cited by 253 · see citing works

PARASITE (RIBEIROIA ONDATRAE) INFECTION LINKED TO AMPHIBIAN MALFORMATIONS IN THE WESTERN UNITED STATES

Johnson, P. T. J., Lunde, K. B., Thurman, E. M., Ritchie, E. G., Wray, S. N., Sutherland, D. R., Kapfer, J. M., Frest, T. J., Bowerman, J., & Blaustein, A. R. (2002) · Ecological Monographs · doi:10.1890/0012-9615(2002)072[0151:proilt]2.0.co;2 · Cited by 247 · see citing works

The role of biotic factors in the transmission of free-living endohelminth stages

Thieltges, D. W., Jensen, K. T., & Poulin, R. (2008) · Parasitology · doi:10.1017/s0031182007000248 · Cited by 241 · see citing works

Pathological and microbiological findings from incidents of unusual mortality of the common frog ( Rana temporaria )

Cunningham, A. A., Langton, T., Bennett, P. M., Lewin, J. F., Drury, S., Gough, R. E., & Macgregor, S. K. (1996) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.1996.0140 · Cited by 240 · see citing works

Interspecific Variation in Susceptibility of Frog Tadpoles to the Pathogenic Fungus Batrachochytrium dendrobatidis

Blaustein, A. R., Romansic, J. M., Scheessele, E. A., Han, B. A., Pessier, A. P., & Longcore, J. E. (2005) · Conservation Biology · doi:10.1111/j.1523-1739.2005.00195.x · Cited by 240 · see citing works

Upward range extension of Andean anurans and chytridiomycosis to extreme elevations in response to tropical deglaciation

Seimon, T. A., Seimon, A., Daszak, P., Halloy, S. R. P., Schloegel, L. M., Aguilar, C., Sowell, P., Hyatt, A. D., Konecky, B., & SIMMONS, J. E. (2006) · Global Change Biology · doi:10.1111/j.1365-2486.2006.01278.x · Cited by 239 · see citing works

Determining environmental causes of biological effects: the need for a mechanistic physiological dimension in conservation biology

Seebacher, F., & Franklin, C. E. (2012) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2012.0036 · Cited by 234 · see citing works

POTENTIAL CAUSES FOR AMPHIBIAN DECLINES IN PUERTO RICO

Burrowes, P. A., Joglar, R. L., & Green, D. E. (2004) · Herpetologica · doi:10.1655/03-50 · Cited by 231 · see citing works

Animal Defenses against Infectious Agents: Is Damage Control More Important Than Pathogen Control

Read, A. F., Graham, A. L., & Råberg, L. (2008) · PLoS Biology · doi:10.1371/journal.pbio.1000004 · Cited by 226 · see citing works

Predicting the Distribution of the Amphibian Pathogen Batrachochytrium dendrobatidis in the New World 1

Ron, S. R. (2005) · Biotropica · doi:10.1111/j.1744-7429.2005.00028.x · Cited by 225 · see citing works

Transmission of Batrachochytrium dendrobatidis within and between amphibian life stages

Rachowicz, L., & Vredenburg, V. T. (2004) · Diseases of Aquatic Organisms · doi:10.3354/dao061075 · Cited by 225 · see citing works

Wild immunology

Pedersen, A. B., & Babayan, S. A. (2011) · Molecular Ecology · doi:10.1111/j.1365-294x.2010.04938.x · Cited by 224 · see citing works

Putting Theory into Practice: Wildlife Health in Conservation

Deem, S. L., Karesh, W. B., & Weisman, W. (2001) · Conservation Biology · doi:10.1046/j.1523-1739.2001.00336.x · Cited by 224 · see citing works

Possible modes of dissemination of the amphibian chytrid Batrachochytrium dendrobatidis in the environment

Johnson, M., & Speare, R. (2005) · Diseases of Aquatic Organisms · doi:10.3354/dao065181 · Cited by 216 · see citing works

Changes in selected aspects of immune function in the leopard frog, Rana pipiens , associated with exposure to cold

Maniero, G. D., & Carey, C. (1997) · Journal of Comparative Physiology B · doi:10.1007/s003600050072 · Cited by 212 · see citing works

Electrolyte depletion and osmotic imbalance in amphibians with chytridiomycosis

Voyles, J., Berger, L., Young, S., Speare, R., Webb, R. J., Warner, J. M., Rudd, D., Campbell, R., & Skerratt, L. F. (2007) · Diseases of Aquatic Organisms · doi:10.3354/dao01838 · Cited by 202 · see citing works

Thermoregulatory behaviour affects prevalence of chytrid fungal infection in a wild population of Panamanian golden frogs

Richards‐Zawacki, C. L. (2009) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2009.1656 · Cited by 202 · see citing works

Experimental Exposures of Boreal Toads (Bufo boreas) to a Pathogenic Chytrid Fungus (Batrachochytrium dendrobatidis)

Carey, C., Bruzgul, J. E., Livo, L. J., Walling, M. L., Kuehl, K. A., Dixon, B. F., Pessier, A. P., Alford, R. A., & Rogers, K. B. (2006) · EcoHealth · doi:10.1007/pl00021734 · Cited by 195 · see citing works

Cutaneous Bacteria of the Redback Salamander Prevent Morbidity Associated with a Lethal Disease

Becker, M. H., & Harris, R. N. (2010) · PLoS ONE · doi:10.1371/journal.pone.0010957 · Cited by 192 · see citing works

Presence of an emerging pathogen of amphibians in introduced bullfrogs Rana catesbeiana in Venezuela

Hanselmann, R., Rodríguez‐Contreras, A., Lampo, M., Fajardo, L., Aguirre, A. A., Kilpatrick, A. M., Rodrı́guez, J. P., & Daszak, P. (2004) · Biological Conservation · doi:10.1016/j.biocon.2004.02.013 · Cited by 189 · see citing works

AMPHIBIAN POPULATION DECLINES AT SAVANNAH RIVER SITE ARE LINKED TO CLIMATE, NOT CHYTRIDIOMYCOSIS

Daszak, P., Scott, D. E., Kilpatrick, A. M., Faggioni, C., Gibbons, J. W., & Porter, D. D. (2005) · Ecology · doi:10.1890/05-0598 · Cited by 188 · see citing works

The complexity of deformed amphibians

Blaustein, A. R., & Johnson, P. T. J. (2003) · Frontiers in Ecology and the Environment · doi:10.1890/1540-9295(2003)001[0087:tcoda]2.0.co;2 · Cited by 188 · see citing works

Amphibian Declines

(2005) · University of California Press eBooks · doi:10.1525/california/9780520235922.001.0001 · Cited by 188 · see citing works

Predicting susceptibility to future declines in the world's frogs

Bielby, J., Cooper, N., Cunningham, A. A., Garner, T. W. J., & Purvis, A. (2008) · Conservation Letters · doi:10.1111/j.1755-263x.2008.00015.x · Cited by 184 · see citing works

Explanation for naturally occurring supernumerary limbs in amphibians

Sessions, S. K., & Ruth, S. B. (1990) · Journal of Experimental Zoology · doi:10.1002/jez.1402540107 · Cited by 184 · see citing works

PATHOLOGY, ISOLATION, AND PRELIMINARY MOLECULAR CHARACTERIZATION OF A NOVEL IRIDOVIRUS FROM TIGER SALAMANDERS IN SASKATCHEWAN

Bollinger, T. K., Mao, J., Schock, D. M., Brigham, R. M., & Chinchar, V. G. (1999) · Journal of Wildlife Diseases · doi:10.7589/0090-3558-35.3.413 · Cited by 183 · see citing works

Antimicrobial peptide defenses against chytridiomycosis, an emerging infectious disease of amphibian populations

Rollins‐Smith, L. A., & Conlon, J. M. (2004) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2004.11.004 · Cited by 181 · see citing works

Infectious Disease Ecology

Ostfeld, R. S., Keesing, F., & Eviner, V. T. (2010) · Princeton University Press eBooks · doi:10.1515/9781400837885 · Cited by 180 · see citing works

ATRAZINE INCREASES RANAVIRUS SUSCEPTIBILITY IN THE TIGER SALAMANDER, AMBYSTOMA TIGRINUM

Forson, D. D., & Storfer, A. T. (2006) · Ecological Applications · doi:10.1890/1051-0761(2006)016[2325:airsit]2.0.co;2 · Cited by 180 · see citing works

EXPERIMENTAL TRANSMISSION OF CUTANEOUS CHYTRIDIOMYCOSIS IN DENDROBATID FROGS

Nichols, D. K., Lamirande, E. W., Pessier, A. P., & Longcore, J. E. (2001) · Journal of Wildlife Diseases · doi:10.7589/0090-3558-37.1.1 · Cited by 178 · see citing works

Characterization of an alarm pheromone secreted by amphibian tadpoles that induces behavioral inhibition and suppression of the neuroendocrine stress axis

Fraker, M. E., Hu, F., Cuddapah, V., McCollum, S. A., Relyea, R. A., Hempel, J. D., & Denver, R. J. (2009) · Hormones and Behavior · doi:10.1016/j.yhbeh.2009.01.007 · Cited by 177 · see citing works

Activity of antimicrobial skin peptides from ranid frogs against Batrachochytrium dendrobatidis, the chytrid fungus associated with global amphibian declines

Rollins‐Smith, L. A., Carey, C., Longcore, J. E., Doersam, J. K., Boutté, A. M., Bruzgal, J. E., & Conlon, J. M. (2002) · Developmental & Comparative Immunology · doi:10.1016/s0145-305x(01)00088-x · Cited by 172 · see citing works

Global Amphibian Extinction Risk Assessment for the Panzootic Chytrid Fungus

Rödder, D., Kielgast, J., Bielby, J., Schmidtlein, S., Bosch, J., Garner, T. W. J., Veith, M., Walker, S., Fisher, M. C., & Lötters, S. (2009) · Diversity · doi:10.3390/d1010052 · Cited by 172 · see citing works

Hormonal Correlates of Environmentally Induced Metamorphosis in the Western Spadefoot Toad,Scaphiopus hammondii

Denver, R. J. (1998) · General and Comparative Endocrinology · doi:10.1006/gcen.1998.7082 · Cited by 170 · see citing works

Host physiological phenotype explains pathogen reservoir potential

Cronin, J. P., Welsh, M. E., Dekkers, M. G. H., Abercrombie, S. T., & Mitchell, C. E. (2010) · Ecology Letters · doi:10.1111/j.1461-0248.2010.01513.x · Cited by 170 · see citing works

Phylogeny, Life History, and Ecology Contribute to Differences in Amphibian Susceptibility to Ranaviruses

Hoverman, J. T., Gray, M. J., Haislip, N. A., & Miller, D. L. (2011) · EcoHealth · doi:10.1007/s10393-011-0717-7 · Cited by 169 · see citing works

Increased Circulating Levels of Testosterone and Corticosterone in Southern Toads,Bufo terrestris,Exposed to Coal Combustion Waste

Hopkins, W. A., Mendonça, M. T., & Congdon, J. D. (1997) · General and Comparative Endocrinology · doi:10.1006/gcen.1997.6969 · Cited by 167 · see citing works

The Transmission of Digenetic Trematodes: Style, Elegance, Complexity

Esch, G. W. (2002) · Integrative and Comparative Biology · doi:10.1093/icb/42.2.304 · Cited by 167 · see citing works

Common Cutaneous Bacteria from the Eastern Red-Backed Salamander Can Inhibit Pathogenic Fungi

Lauer, A., Simon, M. A., Banning, J. L., André, E. A., Duncan, K. L., & Harris, R. N. (2007) · Copeia · doi:10.1643/0045-8511(2007)2007[630:ccbfte]2.0.co;2 · Cited by 167 · see citing works

Comparative immunoecology in birds: hypotheses and tests

Hasselquist, D. (2007) · Journal für Ornithologie · doi:10.1007/s10336-007-0201-x · Cited by 166 · see citing works

Platyhelminth Parasites of the Amphibia

Prudhoe, S., & Bray, R. A. (1982) · Medical Entomology and Zoology · Cited by 165 · see citing works

FUNGAL PATHOGEN CAUSES COMPETITIVE AND DEVELOPMENTAL STRESS IN LARVAL AMPHIBIAN COMMUNITIES

Parris, M. J., & Cornelius, T. O. (2004) · Ecology · doi:10.1890/04-0383 · Cited by 165 · see citing works

Experimental Exposures of Boreal Toads (Bufo boreas) to a Pathogenic Chytrid Fungus (Batrachochytrium dendrobatidis)

Carey, C., Bruzgul, J. E., Livo, L. J., Walling, M. L., Kuehl, K. A., Dixon, B. F., Pessier, A. P., Alford, R. A., & Rogers, K. B. (2005) · EcoHealth · doi:10.1007/s10393-005-0006-4 · Cited by 164 · see citing works

Differential Host Susceptibility to Batrachochytrium dendrobatidis , an Emerging Amphibian Pathogen

Searle, C. L., Gervasi, S. S., Hua, J., Hammond, J. I., Relyea, R. A., Olson, D. H., & Blaustein, A. R. (2011) · Conservation Biology · doi:10.1111/j.1523-1739.2011.01708.x · Cited by 162 · see citing works

Strain differences in the amphibian chytrid Batrachochytrium dendrobatidis and non-permanent, sub-lethal effects of infection

Retallick, R., & Miera, V. (2007) · Diseases of Aquatic Organisms · doi:10.3354/dao075201 · Cited by 161 · see citing works

INTRASPECIFIC RESERVOIRS: COMPLEX LIFE HISTORY AND THE PERSISTENCE OF A LETHAL RANAVIRUS

Brunner, J. L., Schock, D. M., Davidson, E. W., & Collins, J. P. (2004) · Ecology · doi:10.1890/02-0374 · Cited by 161 · see citing works

The Identification of 2,4-diacetylphloroglucinol as an Antifungal Metabolite Produced by Cutaneous Bacteria of the Salamander Plethodon cinereus

Brucker, R. M., Baylor, C. M., Walters, R. L., Lauer, A., Harris, R. N., & Minbiole, K. P. C. (2007) · Journal of Chemical Ecology · doi:10.1007/s10886-007-9352-8 · Cited by 160 · see citing works

Expression Profiling the Temperature-Dependent Amphibian Response to Infection by Batrachochytrium dendrobatidis

Ribas, L., Li, M., Doddington, B. J., Robert, J., Seidel, J. A., Kroll, J. S., Zimmerman, L. B., Grassly, N. C., Garner, T. W. J., & Fisher, M. C. (2009) · PLoS ONE · doi:10.1371/journal.pone.0008408 · Cited by 160 · see citing works

Population trends associated with skin peptide defenses against chytridiomycosis in Australian frogs

Woodhams, D. C., Rollins‐Smith, L. A., Carey, C., Reinert, L. K., Tyler, M. J., & Alford, R. A. (2005) · Oecologia · doi:10.1007/s00442-005-0228-8 · Cited by 160 · see citing works

The contribution of skin antimicrobial peptides to the system of innate immunity in anurans

Conlon, J. M. (2010) · Cell and Tissue Research · doi:10.1007/s00441-010-1014-4 · Cited by 160 · see citing works

Behavioural defense against parasites: interaction with parasite invasiveness

Hart, B. L. (1994) · Parasitology · doi:10.1017/s0031182000085140 · Cited by 160 · see citing works

Experimental evidence for alternative stable equilibria in a benthic pond food web

Chase, J. M. (2003) · Ecology Letters · doi:10.1046/j.1461-0248.2003.00482.x · Cited by 159 · see citing works

Using Simple Models to Predict Virus Epizootics in Gypsy Moth Populations

Dwyer, G., & Elkinton, J. S. (1993) · Journal of Animal Ecology · doi:10.2307/5477 · Cited by 158 · see citing works

Diversity of cutaneous bacteria with antifungal activity isolated from female four-toed salamanders

Lauer, A., Simon, M. A., Banning, J. L., Lam, B. A., & Harris, R. N. (2007) · The ISME Journal · doi:10.1038/ismej.2007.110 · Cited by 157 · see citing works

Development and characterization of a model system to study amphibian immune responses to iridoviruses

Gantress, J., Maniero, G. D., Cohen, N., & Robert, J. (2003) · Virology · doi:10.1016/s0042-6822(03)00151-x · Cited by 155 · see citing works

Addition of antifungal skin bacteria to salamanders ameliorates the effects of chytridiomycosis

Harris, R., Lauer, A., Ma, S., Banning, J. L., & Alford, R. A. (2008) · Diseases of Aquatic Organisms · doi:10.3354/dao02004 · Cited by 154 · see citing works

IMMUNE DEFENSE AND REPRODUCTIVE PACE OF LIFE IN PEROMYSCUS MICE

Martin, L. B., Weil, Z. M., & Nelson, R. J. (2007) · Ecology · doi:10.1890/07-0060.1 · Cited by 151 · see citing works

Role for corticoids in mediating the response of Rana pipiens tadpoles to intraspecific competition

Glennemeier, K. A., & Denver, R. J. (2001) · Journal of Experimental Zoology · doi:10.1002/jez.1140 · Cited by 150 · see citing works

Distribution of Batrachochytrium dendrobatidis and pathology in the skin of green tree frogs Litoria caerulea with severe chytridiomycosis

Berger, L., Speare, R., & Skerratt, L. F. (2005) · Diseases of Aquatic Organisms · doi:10.3354/dao068065 · Cited by 147 · see citing works

Fever: How May Circulating Pyrogens Signal the Brain?

Cm, B., & SEHIC, E. (1997) · Physiology · doi:10.1152/physiologyonline.1997.12.1.1 · Cited by 147 · see citing works

Review of the Trematode Genus Ribeiroia (Psilostomidae): Ecology, Life History and Pathogenesis with Special Emphasis on the Amphibian Malformation Problem

Johnson, P. T. J., Sutherland, D. R., Kinsella, J. M., & Lunde, K. B. (2004) · Advances in Parasitology/Advances in parasitology · doi:10.1016/s0065-308x(04)57003-3 · Cited by 144 · see citing works

Beyond occurrence: Body condition and stress hormone as integrative indicators of habitat availability and fragmentation in the common toad

Janin, A., Léna, J., & Joly, P. B. (2011) · Biological Conservation · doi:10.1016/j.biocon.2010.12.009 · Cited by 143 · see citing works

Interactions between Batrachochytrium dendrobatidis and its amphibian hosts: a review of pathogenesis and immunity

Voyles, J., Rosenblum, E. B., & Berger, L. (2010) · Microbes and Infection · doi:10.1016/j.micinf.2010.09.015 · Cited by 143 · see citing works

Evidence for emergence of an amphibian iridoviral disease because of human‐enhanced spread

Jancovich, J. K., Davidson, E. W., Parameswaran, N., MAO, J., Chinchar, V. G., Collins, J. P., Jacobs, B. L., & Storfer, A. T. (2004) · Molecular Ecology · doi:10.1111/j.1365-294x.2004.02387.x · Cited by 138 · see citing works

Behaviour of Australian rainforest stream frogs may affect the transmission of chytridiomycosis

Rowley, J. J. L., & Alford, R. A. (2007) · Diseases of Aquatic Organisms · doi:10.3354/dao01830 · Cited by 136 · see citing works

A Meta‐Analysis of the Effects of Ultraviolet B Radiation and Its Synergistic Interactions with pH, Contaminants, and Disease on Amphibian Survival

Bancroft, B. A., BAKER, N. J., & Blaustein, A. R. (2008) · Conservation Biology · doi:10.1111/j.1523-1739.2008.00966.x · Cited by 136 · see citing works

High temperature enhances host pathology in a snail–trematode system: possible consequences of climate change for the emergence of disease

Paull, S. H., & Johnson, P. T. J. (2010) · Freshwater Biology · doi:10.1111/j.1365-2427.2010.02547.x · Cited by 134 · see citing works

Escape from the pond: stress and developmental responses to ranavirus infection in wood frog tadpoles

Warne, R. W., Crespi, E. J., & Brunner, J. L. (2010) · Functional Ecology · doi:10.1111/j.1365-2435.2010.01793.x · Cited by 134 · see citing works

Five amphibian mortality events associated with ranavirus infection in south central Ontario, Canada

Greer, A., Berrill, M., & Wilson, P. (2005) · Diseases of Aquatic Organisms · doi:10.3354/dao067009 · Cited by 131 · see citing works

Parasitic and Infectious Disease Responses to Changing Global Nutrient Cycles

McKenzie, V. J., & Townsend, A. R. (2007) · EcoHealth · doi:10.1007/s10393-007-0131-3 · Cited by 127 · see citing works

Diversity and disease: community structure drives parasite transmission and host fitness

Johnson, P. T. J., Hartson, R. B., Larson, D. J., & Sutherland, D. R. (2008) · Ecology Letters · doi:10.1111/j.1461-0248.2008.01212.x · Cited by 127 · see citing works

Influence of temperature on Ranavirus infection in larval salamanders Ambystoma tigrinum

Rojas, S., Richards, K., Jancovich, J. K., & Davidson, E. (2005) · Diseases of Aquatic Organisms · doi:10.3354/dao063095 · Cited by 125 · see citing works

Steroids as Potential Modulators of Thyroid Hormone Activity in Anuran Metamorphosis

Hayes, T. B. (1997) · American Zoologist · doi:10.1093/icb/37.2.185 · Cited by 125 · see citing works

Developmental variation in resistance and tolerance in a multi‐host–parasite system

Rohr, J. R., Raffel, T. R., & Hall, C. A. (2010) · Functional Ecology · doi:10.1111/j.1365-2435.2010.01709.x · Cited by 124 · see citing works

Impaired Adrenocortical Response to Stress by Brown Trout,Salmo trutta,Living in Metal-Contaminated Waters of the Eagle River, Colorado

Norris, D. O., Donahue, S. P., Dores, R. M., Lee, J. K., Maldonado, T. A., Ruth, T., & Woodling, J. D. (1999) · General and Comparative Endocrinology · doi:10.1006/gcen.1998.7177 · Cited by 123 · see citing works

Disease dynamics vary spatially and temporally in a North American amphibian

Savage, A. E., Sredl, M. J., & Zamudio, K. R. (2011) · Biological Conservation · doi:10.1016/j.biocon.2011.03.018 · Cited by 117 · see citing works

A dilution effect in the emerging amphibian pathogen Batrachochytrium dendrobatidis

Searle, C. L., Biga, L. M., Spatafora, J. W., & Blaustein, A. R. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1108490108 · Cited by 117 · see citing works

How Physiological Methods and Concepts Can Be Useful in Conservation Biology

Carey, C. (2005) · Integrative and Comparative Biology · doi:10.1093/icb/45.1.4 · Cited by 114 · see citing works

Effects of the Herbicide Atrazine onAmbystoma tigrinumMetamorphosis: Duration, Larval Growth, and Hormonal Response

Larson, D. L., McDonald, S. F., Fivizzani, A. J., Newton, W. E., & Hamilton, S. J. (1998) · Physiological Zoology · doi:10.1086/515999 · Cited by 113 · see citing works

RANAVIRUS IN WOOD FROGS (RANA SYLVATICA): POTENTIAL SOURCES OF TRANSMISSION WITHIN AND BETWEEN PONDS

Harp, E. M., & Petranka, J. W. (2006) · Journal of Wildlife Diseases · doi:10.7589/0090-3558-42.2.307 · Cited by 112 · see citing works

IN VIVO TESTING OF THE FUNCTIONAL INTEGRITY OF THE CORTICOSTERONE-PRODUCING AXIS IN MUDPUPPY (AMPHIBIA) EXPOSED TO CHLORINATED HYDROCARBONS IN THE WILD

Gendron, A. D., Bishop, C. A., Fortin, R., & Hontela, A. (1997) · Environmental Toxicology and Chemistry · doi:10.1002/etc.5620160818 · Cited by 110 · see citing works

The importance of physiological ecology in conservation biology

Tracy, C. R., Nussear, K. E., Esque, T. C., Dean‐Bradley, K., Tracy, C. R., DeFalco, L. A., Castle, K. T., Zimmerman, L. C., Espinoza, R. E., & Barber, A. M. (2006) · Integrative and Comparative Biology · doi:10.1093/icb/icl054 · Cited by 110 · see citing works

Adaptive Plasticity in Amphibian Metamorphosis: Response of Scaphiopus hammondii Tadpoles to Habitat Desiccation

Denver, R. J., Mirhadi, N., & Phillips, M. (1998) · Ecology · doi:10.2307/176694 · Cited by 110 · see citing works

Toward Immunogenetic Studies of Amphibian Chytridiomycosis: Linking Innate and Acquired Immunity

Richmond, J. Q., Savage, A. E., Zamudio, K. R., & Rosenblum, E. B. (2009) · BioScience · doi:10.1525/bio.2009.59.4.9 · Cited by 109 · see citing works

Global gene expression profiles for life stages of the deadly amphibian pathogen Batrachochytrium dendrobatidis

Rosenblum, E. B., Stajich, J., Maddox, N., & Eisen, M. B. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804173105 · Cited by 108 · see citing works

Parasites, ecosystems and sustainability: an ecological and complex systems perspective

Horwitz, P., & Wilcox, B. A. (2005) · International Journal for Parasitology · doi:10.1016/j.ijpara.2005.03.002 · Cited by 107 · see citing works

Transmission dynamics of the amphibian ranavirus Ambystoma tigrinum virus

Brunner, J. L., Schock, D. M., & Collins, J. (2007) · Diseases of Aquatic Organisms · doi:10.3354/dao01845 · Cited by 105 · see citing works

Glucocorticosteroid Hormone Treatment of Larval Treefrogs Increases Infection by Alaria Sp. Trematode Cercariae

Belden, L. K., & Kiesecker, J. M. (2005) · Journal of Parasitology · doi:10.1645/ge-397r · Cited by 103 · see citing works

Distribution and environmental limitations of an amphibian pathogen in the Rocky Mountains, USA

Muths, E., Pilliod, D. S., & Livo, L. J. (2008) · Biological Conservation · doi:10.1016/j.biocon.2008.03.011 · Cited by 100 · see citing works

Beyond immunity: quantifying the effects of host anti-parasite behavior on parasite transmission

Daly, E. W., & Johnson, P. T. J. (2010) · Oecologia · doi:10.1007/s00442-010-1778-y · Cited by 99 · see citing works

Impacts of Batrachochytrium dendrobatidis Infection on Tadpole Foraging Performance

Venesky, M. D., Parris, M. J., & Storfer, A. T. (2009) · EcoHealth · doi:10.1007/s10393-009-0272-7 · Cited by 99 · see citing works

Development and Disease: How Susceptibility to an Emerging Pathogen Changes through Anuran Development

Haislip, N. A., Gray, M. J., Hoverman, J. T., & Miller, D. L. (2011) · PLoS ONE · doi:10.1371/journal.pone.0022307 · Cited by 98 · see citing works

Disease and the Extended Phenotype: Parasites Control Host Performance and Survival through Induced Changes in Body Plan

Goodman, B. A., & Johnson, P. T. J. (2011) · PLoS ONE · doi:10.1371/journal.pone.0020193 · Cited by 98 · see citing works

Echinostome infection in green frogs (Rana clamitans) is stage and age dependent

Holland, M. P., Skelly, D. K., Kashgarian, M. J., Bolden, S. R., Harrison, L. M., & Cappello, M. (2006) · Journal of Zoology · doi:10.1111/j.1469-7998.2006.00229.x · Cited by 97 · see citing works

The proximate cause of frog declines?

Rosa, I. D., Simoncelli, F., Fagotti, A., & Pascolini, R. (2007) · Nature · doi:10.1038/nature05941 · Cited by 97 · see citing works

What Drives Chytrid Infections in Newt Populations? Associations with Substrate, Temperature, and Shade

Raffel, T. R., Michel, P. J., Sites, E. W., & Rohr, J. R. (2010) · EcoHealth · doi:10.1007/s10393-010-0358-2 · Cited by 93 · see citing works

Effects of environmental change on helminth infections in amphibians: exploring the emergence of Ribeiroia and Echinostoma infections in North America.

Johnson, P. T. J., & McKenzie, V. J. (2008) · Springer eBooks · doi:10.1007/978-0-387-09577-6_11 · Cited by 91 · see citing works

Changes in Stream Primary Producer Communities Resulting from Large-Scale Catastrophic Amphibian Declines: Can Small-Scale Experiments Predict Effects of Tadpole Loss?

Connelly, S., Pringle, C. M., Bixby, R. J., Brenes, R., Whiles, M. R., Lips, K. R., Kilham, S. S., & Huryn, A. D. (2008) · Ecosystems · doi:10.1007/s10021-008-9191-7 · Cited by 91 · see citing works

Morphological Clues from Multilegged Frogs: Are Retinoids to Blame?

Sessions, S. K., Franssen, R. A., & Horner, V. L. (1999) · Science · doi:10.1126/science.284.5415.800 · Cited by 90 · see citing works

MORPHOLOGICAL ABNORMALITY PATTERNS IN A CALIFORNIA AMPHIBIAN COMMUNITY

Johnson, P. T. J., Lunde, K. B., Ritchie, E. G., Reaser, J. K., & Launer, A. E. (2001) · Deakin Research Online (Deakin University) · Cited by 90 · see citing works

Critical windows of disease risk: amphibian pathology driven by developmental changes in host resistance and tolerance

Johnson, P. T. J., Kellermanns, E., & Bowerman, J. (2011) · Functional Ecology · doi:10.1111/j.1365-2435.2010.01830.x · Cited by 89 · see citing works

First case of ranavirus-associated morbidity and mortality in natural populations of the South American frog Atelognathus patagonicus

Fox, S. F., Greer, A., Torres-Cervantes, R., & Collins, J. (2006) · Diseases of Aquatic Organisms · doi:10.3354/dao072087 · Cited by 89 · see citing works

IDENTIFICATION OF THE NATURAL BACTERIAL MICROFLORA ON THE SKIN OF EASTERN NEWTS, BULLFROG TADPOLES AND REDBACK SALAMANDERS

Culp, C. E., Falkinham, J. O., & Belden, L. K. (2007) · Herpetologica · doi:10.1655/0018-0831(2007)63[66:iotnbm]2.0.co;2 · Cited by 88 · see citing works

Impacts of agriculture on the parasite communities of northern leopard frogs (Rana pipiens) in southern Quebec, Canada

King, K. C., McLaughlin, J., Gendron, A. D., Pauli, B. D., GIROUX, I., Rondeau, B., Boily, M. H., Juneau, P., & Marcogliese, D. J. (2007) · Parasitology · doi:10.1017/s0031182007003277 · Cited by 85 · see citing works

Frog virus 3 prevalence in tadpole populations inhabiting cattle-access and non-access wetlands in Tennessee, USA

Gray, M., Miller, D. L., Schmutzer, A. C., & Baldwin, C. (2007) · Diseases of Aquatic Organisms · doi:10.3354/dao01837 · Cited by 84 · see citing works

Influence of Ribeiroia ondatrae (Trematoda: Digenea) infection on limb development and survival of northern leopard frogs (Rana pipiens): effects of host stage and parasite-exposure level

Schotthoefer, A. M., Koehler, A. V. A., Meteyer, C. U., & Cole, R. A. (2003) · Canadian Journal of Zoology · doi:10.1139/z03-099 · Cited by 81 · see citing works

Global warming and biodiversity: Evidence of climate-linked amphibian declines in Italy

D‘Amen, M., & Bombi, P. (2009) · Biological Conservation · doi:10.1016/j.biocon.2009.08.004 · Cited by 77 · see citing works

Morphological and behavioural responses of frog tadpoles to perceived predation risk: A possible role for corticosterone mediation?

Hossie, T. J., Ferland‐Raymond, B., Burness, G., & Murray, D. L. (2010) · Ecoscience · doi:10.2980/17-1-3312 · Cited by 72 · see citing works

Chytridiomycosis impacts predator-prey interactions in larval amphibian communities

Parris, M. J., & Beaudoin, J. G. (2004) · Oecologia · doi:10.1007/s00442-004-1631-2 · Cited by 71 · see citing works

ENVIRONMENTAL FACTORS INFLUENCING TREMATODE PREVALENCE IN GREY TREE FROG (HYLA VERSICOLOR) TADPOLES IN SOUTHERN ONTARIO

Koprivnikar, J., Baker, R. L., & Forbes, M. R. (2006) · Journal of Parasitology · doi:10.1645/ge-771r.1 · Cited by 71 · see citing works

Comparison of Hematological Stress Indicators in Recently Captured and Captive Paedomorphic Mole Salamanders, Ambystoma talpoideum

Davis, A. K., & Maerz, J. C. (2008) · Copeia · doi:10.1643/cp-07-133 · Cited by 68 · see citing works

Chemotaxis of the amphibian pathogen Batrachochytrium dendrobatidis and its response to a variety of attractants

Moss, A. S., Reddy, N. S., Dortaj, I. M., & Francisco, M. J. S. (2008) · Mycologia · doi:10.3852/mycologia.100.1.1 · Cited by 68 · see citing works

Effects of agricultural landscape and pesticides on parasitism in native bullfrogs

King, K. C., McLaughlin, J., Boily, M. H., & Marcogliese, D. J. (2009) · Biological Conservation · doi:10.1016/j.biocon.2009.10.011 · Cited by 67 · see citing works

Immune defenses of Xenopus laevis against Batrachochytrium dendrobatidis

Rollins‐Smith, L. A. (2009) · Frontiers in Bioscience-Scholar · doi:10.2741/s8 · Cited by 65 · see citing works

Pathology, isolation and molecular characterisation of a ranavirus from the common midwife toad Alytes obstetricans on the Iberian Peninsula

Balseiro, A., Dalton, K. P., del Cerro, A., Márquez, I., Cunningham, A. A., Parra, F., Prieto, J., & Casais, R. (2009) · Diseases of Aquatic Organisms · doi:10.3354/dao02032 · Cited by 64 · see citing works

Predicting organismal vulnerability to climate warming: roles of behaviour, physiology and adaptation

Huey, R. B., Kearney, M., Krockenberger, A. K., Holtum, J. A. M., Jess, M., & Williams, S. E. (2012) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2012.0005 · Cited by 1,443 · see citing works

Climate-driven declines in arthropod abundance restructure a rainforest food web

Lister, B. C., & Garcia, A. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1722477115 · Cited by 730 · see citing works

What is conservation physiology? Perspectives on an increasingly integrated and essential science

Cooke, S. J., Sack, L., Franklin, C. E., Farrell, A. P., Beardall, J., Wikelski, M. C., & Chown, S. L. (2013) · Conservation Physiology · doi:10.1093/conphys/cot001 · Cited by 491 · see citing works

Determining environmental causes of biological effects: the need for a mechanistic physiological dimension in conservation biology

Seebacher, F., & Franklin, C. E. (2012) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2012.0036 · Cited by 234 · see citing works

The relationship between physiological stress and wildlife disease: consequences for health and conservation

Hing, S., Narayan, E. J., Thompson, R. C. A., & Godfrey, S. S. (2016) · Wildlife Research · doi:10.1071/wr15183 · Cited by 183 · see citing works

The use of glucocorticoid hormones or leucocyte profiles to measure stress in vertebrates: What’s the difference?

Davis, A. K., & Maney, D. L. (2018) · Methods in Ecology and Evolution · doi:10.1111/2041-210x.13020 · Cited by 164 · see citing works

Ecophysiology of avian migration in the face of current global hazards

Klaassen, M., Hoye, B. J., Nolet, B. A., & Buttemer, W. A. (2012) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2012.0008 · Cited by 146 · see citing works

Physiology, Behavior, and Conservation

Cooke, S. J., Blumstein, D. T., Buchholz, R., Caro, T., Fernández‐Juricic, E., Franklin, C. E., Metcalfe, J. D., O’Connor, C. M., Clair, C. C. S., Sutherland, W. J., et al. (2013) · Physiological and Biochemical Zoology · doi:10.1086/671165 · Cited by 144 · see citing works

Patterns and biases in climate change research on amphibians and reptiles: a systematic review

Winter, M., Fiedler, W., Hochachka, W. M., Koehncke, A., Meiri, S., & la Riva, I. D. (2016) · Royal Society Open Science · doi:10.1098/rsos.160158 · Cited by 143 · see citing works

Conservation physiology in practice: how physiological knowledge has improved our ability to sustainably manage Pacific salmon during up-river migration

Cooke, S. J., Hinch, S. G., Donaldson, M., Clark, T. D., Eliason, E. J., Crossin, G. T., Raby, G. D., Jeffries, K. M., Lapointe, M., Miller, K. M., et al. (2012) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2012.0022 · Cited by 131 · see citing works

Applications and implications of ecological energetics

Tomlinson, S., Arnall, S. G., Munn, A. J., Bradshaw, D., Maloney, S. K., Dixon, K. W., & Didham, R. K. (2014) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2014.03.003 · Cited by 126 · see citing works

Panamanian frog species host unique skin bacterial communities

Belden, L. K., Hughey, M. C., Rebollar, E. A., Umile, T. P., Loftus, S. C., Burzynski, E. A., Minbiole, K. P. C., House, L., Jensen, R. V., Becker, M. H., et al. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.01171 · Cited by 117 · see citing works

Hormonally mediated maternal effects, individual strategy and global change

Meylan, S., Miles, D. B., & Clobert, J. (2012) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2012.0020 · Cited by 114 · see citing works

Ranavirus Ecology and Evolution: From Epidemiology to Extinction

Brunner, J. L., Storfer, A. T., Gray, M. J., & Hoverman, J. T. (2015) · Springer eBooks · doi:10.1007/978-3-319-13755-1_4 · Cited by 113 · see citing works

Ranaviruses: lethal pathogens of ectothermic vertebrates

(2015) · Choice Reviews Online · doi:10.5860/choice.192841 · Cited by 112 · see citing works

Clade‐specific consequences of climate change to amphibians in Atlantic Forest protected areas

Loyola, R. A., Lemes, P., Brum, F. T., Provete, D. B., & Duarte, L. (2013) · Ecography · doi:10.1111/j.1600-0587.2013.00396.x · Cited by 104 · see citing works

20 Years of fish immunotoxicology – what we know and where we are

Rehberger, K., Werner, I., Hitzfeld, B., Segner, H. E., & Baumann, L. (2017) · Critical Reviews in Toxicology · doi:10.1080/10408444.2017.1288024 · Cited by 103 · see citing works

Heterogeneous Occupancy and Density Estimates of the Pathogenic Fungus Batrachochytrium dendrobatidis in Waters of North America

Chestnut, T., Anderson, C. W., Popa, R., Blaustein, A. R., Voytek, M. A., Olson, D. H., & Kirshtein, J. D. (2014) · PLoS ONE · doi:10.1371/journal.pone.0106790 · Cited by 98 · see citing works

Sickness behaviors across vertebrate taxa: proximate and ultimate mechanisms

Lopes, P. C., French, S. S., Woodhams, D. C., & Binning, S. A. (2021) · Journal of Experimental Biology · doi:10.1242/jeb.225847 · Cited by 96 · see citing works

Extreme drought, host density, sex, and bullfrogs influence fungal pathogen infection in a declining lotic amphibian

Adams, A. J., Kupferberg, S. J., Wilber, M. Q., Pessier, A. P., Grefsrud, M., Bobzien, S., Vredenburg, V. T., & Briggs, C. J. (2017) · Ecosphere · doi:10.1002/ecs2.1740 · Cited by 89 · see citing works

Host Identity Matters in the Amphibian-Batrachochytrium dendrobatidis System: Fine-Scale Patterns of Variation in Responses to a Multi-Host Pathogen

Gervasi, S. S., Gondhalekar, C., Olson, D. H., & Blaustein, A. R. (2013) · PLoS ONE · doi:10.1371/journal.pone.0054490 · Cited by 89 · see citing works

A Non-Invasive Stress Assay Shows That Tadpole Populations Infected with Batrachochytrium dendrobatidis Have Elevated Corticosterone Levels

Gabor, C. R., Fisher, M. C., & Bosch, J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0056054 · Cited by 87 · see citing works

The conservation physiology of seed dispersal

Ruxton, G. D., & Schaefer, H. M. (2012) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2012.0001 · Cited by 86 · see citing works

Physiology in conservation translocations

Tarszisz, E., Dickman, C. R., & Munn, A. J. (2014) · Conservation Physiology · doi:10.1093/conphys/cou054 · Cited by 83 · see citing works

Ranaviruses

Gray, M. J., & Chinchar, V. G. (2015) · Springer eBooks · doi:10.1007/978-3-319-13755-1 · Cited by 80 · see citing works

Application of genetics and genomics to wildlife epidemiology

Blanchong, J. A., Robinson, S. J., Samuel, M. D., & Foster, J. T. (2016) · Journal of Wildlife Management · doi:10.1002/jwmg.1064 · Cited by 80 · see citing works

Nutrition and health in amphibian husbandry

Ferrie, G. M., Alford, V., Atkinson, J. L., Baitchman, E. J., Barber, D. M., Blaner, W. S., Crawshaw, G. J., Daneault, A., Dierenfeld, E. S., Finke, M. D., et al. (2014) · Zoo Biology · doi:10.1002/zoo.21180 · Cited by 75 · see citing works

Using physiology to understand climate-driven changes in disease and their implications for conservation

Rohr, J. R., Raffel, T. R., Blaustein, A. R., Johnson, P. T. J., Paull, S. H., & Young, S. (2013) · Conservation Physiology · doi:10.1093/conphys/cot022 · Cited by 71 · see citing works

Host–multiparasite interactions in amphibians: a review

Herczeg, D., Ujszegi, J., Kásler, A., Holly, D., & Hettyey, A. (2021) · Parasites & Vectors · doi:10.1186/s13071-021-04796-1 · Cited by 71 · see citing works

Elevated Corticosterone Levels and Changes in Amphibian Behavior Are Associated with Batrachochytrium dendrobatidis (Bd) Infection and Bd Lineage

Gabor, C. R., Fisher, M. C., & Bosch, J. (2015) · PLoS ONE · doi:10.1371/journal.pone.0122685 · Cited by 61 · see citing works

Climate change from an ectotherm perspective: evolutionary consequences and demographic change in amphibian and reptilian populations

Bofill, S. I. H., & Blom, M. P. K. (2024) · Biodiversity and Conservation · doi:10.1007/s10531-023-02772-y · Cited by 50 · see citing works

Effects of road salt on larval amphibian susceptibility to parasitism through behavior and immunocompetence

Milotic, D., Milotic, M., & Koprivnikar, J. (2017) · Aquatic Toxicology · doi:10.1016/j.aquatox.2017.05.015 · Cited by 48 · see citing works

Temporal patterns in immunity, infection load and disease susceptibility: understanding the drivers of host responses in the amphibian‐chytrid fungus system

Gervasi, S. S., Hunt, E. G., Lowry, M. B., & Blaustein, A. R. (2013) · Functional Ecology · doi:10.1111/1365-2435.12194 · Cited by 48 · see citing works

Repeated thermal stressor causes chronic elevation of baseline corticosterone and suppresses the physiological endocrine sensitivity to acute stressor in the cane toad (Rhinella marina)

Narayan, E. J., & Hero, J. (2014) · Journal of Thermal Biology · doi:10.1016/j.jtherbio.2014.02.011 · Cited by 45 · see citing works

Reduced immune function predicts disease susceptibility in frogs infected with a deadly fungal pathogen

Savage, A. E., Terrell, K. A., Gratwicke, B., Mattheus, N. M., Augustine, L., & Fleischer, R. C. (2016) · Conservation Physiology · doi:10.1093/conphys/cow011 · Cited by 43 · see citing works

Skin sloughing rate increases with chytrid fungus infection load in a susceptible amphibian

Ohmer, M. E. B., Cramp, R. L., White, C. R., & Franklin, C. E. (2014) · Functional Ecology · doi:10.1111/1365-2435.12370 · Cited by 43 · see citing works

Exploring the link between ultraviolet B radiation and immune function in amphibians: implications for emerging infectious diseases

Cramp, R. L., & Franklin, C. E. (2018) · Conservation Physiology · doi:10.1093/conphys/coy035 · Cited by 42 · see citing works

Effects of Polyester Microplastic Fiber Contamination on Amphibian–Trematode Interactions

Buss, N., Sander, B., & Hua, J. (2021) · Environmental Toxicology and Chemistry · doi:10.1002/etc.5035 · Cited by 42 · see citing works

Characterization of the Skin Microbiota in Italian Stream Frogs (Rana italica) Infected and Uninfected by a Cutaneous Parasitic Disease

Federici, E., Rossi, R., Fidati, L., Paracucchi, R., Scargetta, S., Montalbani, E., Franzetti, A., Porta, G. L., Fagotti, A., Simoncelli, F., et al. (2015) · Microbes and Environments · doi:10.1264/jsme2.me15041 · Cited by 40 · see citing works

Sequestered Alkaloid Defenses in the Dendrobatid Poison Frog Oophaga pumilio Provide Variable Protection from Microbial Pathogens

Hovey, K. J., Seiter, E. M., Johnson, E. E., & Saporito, R. A. (2018) · Journal of Chemical Ecology · doi:10.1007/s10886-018-0930-8 · Cited by 39 · see citing works

Experimental infection dynamics: using immunosuppression andin vivoparasite tracking to understand host resistance in an amphibian-trematode system

LaFonte, B. E., & Johnson, P. T. J. (2013) · Journal of Experimental Biology · doi:10.1242/jeb.088104 · Cited by 38 · see citing works

Shifts in temperature influence how Batrachochytrium dendrobatidis infects amphibian larvae

Bradley, P. W., Brawner, M. D., Raffel, T. R., Rohr, J. R., Olson, D. H., & Blaustein, A. R. (2019) · PLoS ONE · doi:10.1371/journal.pone.0222237 · Cited by 37 · see citing works

Beyond the disease: Is Toxoplasma gondii infection causing population declines in the eastern quoll (Dasyurus viverrinus)?

Fancourt, B. A., Nicol, S. C., Hawkins, C. E., Jones, M. E., & Johnson, C. N. (2014) · International Journal for Parasitology Parasites and Wildlife · doi:10.1016/j.ijppaw.2014.05.001 · Cited by 37 · see citing works

Interaction between temperature and sublethal infection with the amphibian chytrid fungus impacts a susceptible frog species

Campbell, L., Bower, D. S., Clulow, S., Stockwell, M. P., Clulow, J., & Mahony, M. J. (2019) · Scientific Reports · doi:10.1038/s41598-018-35874-7 · Cited by 35 · see citing works

Towards a more healthy conservation paradigm: integrating disease and molecular ecology to aid biological conservation†

Gupta, P., Robin, V. V., & Dharmarajan, G. (2020) · Journal of Genetics · doi:10.1007/s12041-020-01225-7 · Cited by 35 · see citing works

Effects of corticosterone on infection and disease in salamanders exposed to the amphibian fungal pathogen Batrachochytrium dendrobatidis

Fonner, C., Patel, S., Boord, S., Venesky, M., & Woodley, S. K. (2016) · Diseases of Aquatic Organisms · doi:10.3354/dao03089 · Cited by 32 · see citing works

Identifying the presence of microplastics in frogs from the largest delta of the world

Shetu, M. H., Parvin, F., & Tareq, S. M. (2023) · Environmental Advances · doi:10.1016/j.envadv.2023.100355 · Cited by 31 · see citing works

Larval exposure to predator cues alters immune function and response to a fungal pathogen in post‐metamorphic wood frogs

Groner, M. L., Buck, J. C., Gervasi, S. S., Blaustein, A. R., Reinert, L. K., Rollins‐Smith, L. A., Bier, M. E., Hempel, J. D., & Relyea, R. A. (2013) · Ecological Applications · doi:10.1890/12-1572.1 · Cited by 30 · see citing works

Microclimate limits thermal behaviour favourable to disease control in a nocturnal amphibian

Beukema, W., Pasmans, F., Praet, S. V., Ferri‐Yáñez, F., Kelly, M., Laking, A. E., Erens, J., Speybroeck, J., Verheyen, K., Lens, L., et al. (2020) · Ecology Letters · doi:10.1111/ele.13616 · Cited by 30 · see citing works

Cryptic impacts of temperature variability on amphibian immune function

Terrell, K. A., Quintero, R. P., Murray, S. Z., Kleopfer, J. D., Murphy, J. B., Evans, M. J., Nissen, B. D., & Gratwicke, B. (2013) · Journal of Experimental Biology · doi:10.1242/jeb.089896 · Cited by 29 · see citing works

Critical disease windows shaped by stress exposure alter allocation trade‐offs between development and immunity

Kirschman, L. J., Crespi, E. J., & Warne, R. W. (2017) · Journal of Animal Ecology · doi:10.1111/1365-2656.12778 · Cited by 29 · see citing works

Predators and trematode parasites jointly affect larval anuran functional traits and corticosterone levels

Marino, J. A., Holland, M. P., & Maher, J. M. (2013) · Oikos · doi:10.1111/j.1600-0706.2013.00896.x · Cited by 29 · see citing works

Conservation implications of physiological carry‐over effects in bats recovering from white‐nose syndrome

Davy, C. M., Mastromonaco, G. F., Riley, J. L., Baxter‐Gilbert, J. H., Mayberry, H. W., & Willis, C. K. R. (2016) · Conservation Biology · doi:10.1111/cobi.12841 · Cited by 28 · see citing works

Dietary antioxidants enhance immunocompetence in larval amphibians

Szuroczki, D., Koprivnikar, J., & Baker, R. L. (2016) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2016.07.014 · Cited by 23 · see citing works

Framework for multi-stressor physiological response evaluation in amphibian risk assessment and conservation

Awkerman, J. A., Glinski, D. A., Henderson, W. M., Meter, R. J. V., & Purucker, S. T. (2024) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2024.1336747 · Cited by 24 · see citing works

Roundup™ With Corticosterone Functions as an Infodisruptor to Antipredator Response in Tadpoles

Gabor, C. R., Perkins, H. R., Heitmann, A. T., Forsburg, Z. R., & Aspbury, A. S. (2019) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2019.00114 · Cited by 22 · see citing works

Effects of Echinostoma trivolvis metacercariae infection during development and metamorphosis of the wood frog (Lithobates sylvaticus)

Orlofske, S. A., Belden, L. K., & Hopkins, W. A. (2016) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2016.08.002 · Cited by 21 · see citing works

Time-delayed influence of urban landscape change on the susceptibility of koalas to chlamydiosis

McAlpine, C., Brearley, G., Rhodes, J., Bradley, A., Baxter, G., Seabrook, L., Lunney, D., Liu, Y., Cottin, M., Smith, A. G., et al. (2017) · Landscape Ecology · doi:10.1007/s10980-016-0479-2 · Cited by 18 · see citing works

The anurofauna of a vanishing savanna: the case of the Brazilian Cerrado

Ribeiro, J., Colli, G. R., & Soares, A. M. V. M. (2017) · Biodiversity and Conservation · doi:10.1007/s10531-017-1468-8 · Cited by 21 · see citing works

Trends in Ranavirus Prevalence Among Plethodontid Salamanders in the Great Smoky Mountains National Park

Sutton, W. B., Gray, M. J., Hoverman, J. T., Secrist, R. G., Super, P. E., Hardman, R., Tucker, J. L., & Miller, D. L. (2014) · EcoHealth · doi:10.1007/s10393-014-0994-z · Cited by 20 · see citing works

High juvenile mortality in amphibians during overwintering related to fungal pathogen exposure

Rumschlag, S. L., & Boone, M. D. (2018) · Diseases of Aquatic Organisms · doi:10.3354/dao03277 · Cited by 20 · see citing works

Myxosporean parasites in Australian frogs: Importance, implications and future directions

Hartigan, A., Phalen, D. N., & Šlapeta, J. R. (2013) · International Journal for Parasitology Parasites and Wildlife · doi:10.1016/j.ijppaw.2012.12.002 · Cited by 19 · see citing works

UV exposure causes energy trade-offs leading to increased chytrid fungus susceptibility in green tree frog larvae

Cramp, R. L., Ohmer, M. E. B., & Franklin, C. E. (2022) · Conservation Physiology · doi:10.1093/conphys/coac038 · Cited by 17 · see citing works

Level of UV-B radiation influences the effects of glyphosate-based herbicide on the spotted salamander

Levis, N. A., & Johnson, J. R. (2015) · Ecotoxicology · doi:10.1007/s10646-015-1448-2 · Cited by 19 · see citing works

Phenological mismatches mitigate the ecological impact of a biological invader on amphibian communities

Everts, T., Driessche, C. V., Neyrinck, S., Haegeman, A., Ruttink, T., Jacquemyn, H., & Brys, R. (2024) · Ecological Applications · doi:10.1002/eap.3017 · Cited by 18 · see citing works

Is It Worth the Risk? Food Deprivation Effects on Tadpole Anti-Predatory Responses

Gazzola, A., Balestrieri, A., Martín, J. M., & Pellitteri‐Rosa, D. (2017) · Evolutionary Biology · doi:10.1007/s11692-017-9430-y · Cited by 18 · see citing works

Endocrine and immune responses of larval amphibians to trematode exposure

Koprivnikar, J., Hoye, B. J., Urichuk, T. M. Y., & Johnson, P. T. J. (2018) · Parasitology Research · doi:10.1007/s00436-018-6154-6 · Cited by 17 · see citing works

Experimental exposure indicates the amphibian chytrid pathogen poses low risk to N ew Z ealand's threatened endemic frogs

Ohmer, M. E. B., Herbert, S. M., Speare, R., & Bishop, P. J. (2012) · Animal Conservation · doi:10.1111/acv.12010 · Cited by 17 · see citing works

Precipitation Constrains Amphibian Chytrid Fungus Infection Rates in a Terrestrial Frog Assemblage in Jamaica, West Indies

Holmes, I. A., McLaren, K., & Wilson, B. S. (2014) · Biotropica · doi:10.1111/btp.12093 · Cited by 16 · see citing works

Intensive vehicle traffic impacts morphology and endocrine stress response in a threatened amphibian

Cayuela, H., Quay, L., Dumet, A., Léna, J., Miaud, C., & Rivière, V. (2015) · Oryx · doi:10.1017/s0030605315000812 · Cited by 16 · see citing works

First case of ranavirus and associated morbidity and mortality in an eastern mud turtle Kinosternon subrubrum in South Carolina

Winzeler, M. E., Hamilton, M., Tuberville, T. D., & Lance, S. L. (2015) · Diseases of Aquatic Organisms · doi:10.3354/dao02849 · Cited by 16 · see citing works

Quantifying larval trematode infections in hosts: A comparison of method validity and implications for infection success

LaFonte, B. E., Raffel, T. R., Monk, I. N., & Johnson, P. T. J. (2015) · Experimental Parasitology · doi:10.1016/j.exppara.2015.04.003 · Cited by 15 · see citing works

Host stress physiology and Trypanosoma haemoparasite infection influence innate immunity in the woylie ( Bettongia penicillata )

Hing, S., Currie, A. J., Broomfield, S., Keatley, S. K., Jones, K. L., Thompson, R. C. A., Narayan, E. J., & Godfrey, S. S. (2016) · Comparative Immunology Microbiology and Infectious Diseases · doi:10.1016/j.cimid.2016.04.005 · Cited by 15 · see citing works

Sub-chronic exposure to a neonicotinoid does not affect susceptibility of larval leopard frogs to infection by trematode parasites, via either depressed cercarial performance or host immunity

Robinson, S. A., Gavel, M. J., Richardson, S. D., Chlebak, R. J., Milotic, D., Koprivnikar, J., & Forbes, M. R. (2019) · Parasitology Research · doi:10.1007/s00436-019-06385-9 · Cited by 15 · see citing works

Researcher perspectives on challenges and opportunities in conservation physiology revealed from an online survey

Madliger, C. L., Love, O. P., Nguyen, V. M., Haddaway, N., & Cooke, S. J. (2021) · Conservation Physiology · doi:10.1093/conphys/coab030 · Cited by 14 · see citing works

Mechanisms Contributing to the Emergence of Ranavirus in Ectothermic Vertebrate Communities

Brenes, R. (2013) · Cited by 14 · see citing works

Development of reverse-transcriptase quantitative PCR assays for detection of the cytokines IL-1β, TNF-α, and IL-10 in chelonians

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Blaustein, A. R., Gervasi, S. S., Bradley, P., Xie, G., Bradley, P. W., Xie, G. Y., Blaustein, A. R., Gervasi, S. S., Johnson, P. T. J., Hoverman, J. T., et al. (2016)