Arias, P. A. et al. Technical summary. in Climate Change 2021: The Physical Science Basis. Contribution of Working Group I to the Sixth Assessment Report of the Intergovernmental Panel on Climate Change (2021).
Pinsky, M. L., Eikeset, A. M., McCauley, D. J., Payne, J. L. & Sunday, J. M. Greater vulnerability to warming of marine versus terrestrial ectotherms. Nature 569, 108–111 (2019).
Google Scholar
Sunday, J. M., Bates, A. E. & Dulvy, N. K. Thermal tolerance and the global redistribution of animals. Nat. Clim. Chang. 2, 686–690 (2012).
Google Scholar
Fry, F. Effects of the environment on animal activity. Publ. Ontario Fish. Res. Lab. 55, 1–62 (1947).
Lutterschmidt, W. I. & Hutchison, V. H. The critical thermal maximum: history and critique. Can. J. Zool. 75, 1561–1574, https://doi.org/10.1139/z97-783 (2011).
Google Scholar
Rezende, E. L., Castañeda, L. E. & Santos, M. Tolerance landscapes in thermal ecology. Funct. Ecol. 28, 799–809 (2014).
Google Scholar
Bozinovic, F., Calosi, P. & Spicer, J. I. Physiological correlates of geographic range in animals. Annu. Rev. Ecol. Evol. S. 42, 155–179 (2011).
Google Scholar
Sunday, J. M. et al. Thermal-safety margins and the necessity of thermoregulatory behavior across latitude and elevation. Proc. Natl. Acad. Sci. USA 111, 5610–5615 (2014).
Google Scholar
Deutsch, C. A. et al. Impacts of climate warming on terrestrial ectotherms across latitude. Proc. Natl. Acad. Sci. USA 105, 6668–6672 (2008).
Google Scholar
Comte, L. & Olden, J. D. Climatic vulnerability of the world’s freshwater and marine fishes. Nat. Clim. Chang. 7, 718–722 (2017).
Google Scholar
Dahlke, F. T., Wohlrab, S., Butzin, M. & Pörtner, H.-O. Thermal bottlenecks in the life cycle define climate vulnerability of fish. Science 369, 65–70 (2020).
Google Scholar
Pottier, P., Burke, S., Drobniak, S. M. & Nakagawa, S. Methodological inconsistencies define thermal bottlenecks in fish life cycle: a comment on Dahlke et al. 2020. Evol. Ecol. 36, 287–292 (2022).
Google Scholar
Dahlke, F., Butzin, M., Wohlrab, S. & Pörtner, H.-O. Reply to: methodological inconsistencies define thermal bottlenecks in fish life cycle. Evol. Ecol. 36, 293–298 (2022).
Google Scholar
Pottier, P. et al. Developmental plasticity in thermal tolerance: Ontogenetic variation, persistence, and future directions. Ecol. Lett. (2022).
Morley, S. A., Peck, L. S., Sunday, J. M., Heiser, S. & Bates, A. E. Physiological acclimation and persistence of ectothermic species under extreme heat events. Glob. Ecol. Biogeogr. 28, 1018–1037 (2019).
Google Scholar
Rohr, J. R. et al. The complex drivers of thermal acclimation and breadth in ectotherms. Ecol. Lett. 21, 1425–1439 (2018).
Google Scholar
Gunderson, A. R. & Stillman, J. H. Plasticity in thermal tolerance has limited potential to buffer ectotherms from global warming. Proc. R. Soc. B-Biol. Sci. 282, 20150401 (2015).
Google Scholar
Weaving, H., Terblanche, J. S., Pottier, P. & English, S. Meta-analysis reveals weak but pervasive plasticity in insect thermal limits. Nat. Commun. 13, 1–11 (2022).
Google Scholar
Araújo, M. B. et al. Heat freezes niche evolution. Ecol. Lett. 16, 1206–1219 (2013).
Google Scholar
Bennett, J. M. et al. The evolution of critical thermal limits of life on Earth. Nat. Commun. 12, 1198 (2021).
Google Scholar
Hoffmann, A. A., Chown, S. L. & Clusella-Trullas, S. Upper thermal limits in terrestrial ectotherms: how constrained are they? Funct. Ecol. 27, 934–949 (2013).
Google Scholar
Kellermann, V. et al. Upper thermal limits of Drosophila are linked to species distributions and strongly constrained phylogenetically. Proc. Natl. Acad. Sci. USA 109, 16228–16233 (2012).
Google Scholar
Morgan, R., Finnøen, M. H., Jensen, H., Pélabon, C. & Jutfelt, F. Low potential for evolutionary rescue from climate change in a tropical fish. Proc. Natl. Acad. Sci. USA 117, 33365–33372 (2020).
Google Scholar
Bennett, J. M. et al. GlobTherm, a global database on thermal tolerances for aquatic and terrestrial organisms. Sci. Data 5, 180022 (2018).
Google Scholar
Leiva, F. P., Calosi, P. & Verberk, W. C. E. P. Scaling of thermal tolerance with body mass and genome size in ectotherms: a comparison between water- and air-breathers. Philos. Trans. R. Soc. B-Biol. Sci. 374, 20190035 (2019).
Google Scholar
Clusella-Trullas, S., Blackburn, T. M. & Chown, S. L. Climatic predictors of temperature performance curve parameters in ectotherms imply complex responses to climate change. Am. Nat. 177, 738–751 (2011).
Google Scholar
Nakagawa, S. & Freckleton, R. P. Missing inaction: the dangers of ignoring missing data. Trends Ecol. Evol. 23, 592–596 (2008).
Google Scholar
Johnson, T. F., Isaac, N. J. B., Paviolo, A. & González-Suárez, M. Handling missing values in trait data. Glob. Ecol. Biogeogr. 30, 51–62 (2021).
Google Scholar
Foo, Y. Z., O’Dea, R. E., Koricheva, J., Nakagawa, S. & Lagisz, M. A practical guide to question formation, systematic searching and study screening for literature reviews in ecology and evolution. Methods Ecol. Evol. 12, 1705–1720 (2021).
Google Scholar
Reboredo Segovia, A. L., Romano, D. & Armsworth, P. R. Who studies where? Boosting tropical conservation research where it is most needed. Front. Ecol. Environ. 18, 159–166 (2020).
Google Scholar
White, C. R. et al. Geographical bias in physiological data limits predictions of global change impacts. Funct. Ecol. 35, 1572–1578 (2021).
Google Scholar
Amano, T., González-Varo, J. P. & Sutherland, W. J. Languages are still a major barrier to global Science. PLoS Biol. 14, e2000933 (2016).
Google Scholar
Bennett, S., Duarte, C. M., Marbà, N. & Wernberg, T. Integrating within-species variation in thermal physiology into climate change ecology. Philos. Trans. R. Soc. B-Biol. Sci. 374, 20180550 (2019).
Google Scholar
Noble, D. W. A. et al. Meta-analytic approaches and effect sizes to account for ‘nuisance heterogeneity’ in comparative physiology. J. Exp. Biol. 225, jeb243225 (2022).
Google Scholar
Peralta-Maraver, I. & Rezende, E. L. Heat tolerance in ectotherms scales predictably with body size. Nat. Clim. Chang. 11, 58–63 (2021).
Google Scholar
McKenzie, D. J. et al. Intraspecific variation in tolerance of warming in fishes. J. Fish Biol. 98, 1536–1555 (2021).
Google Scholar
Morrissey, M. B. Meta-analysis of magnitudes, differences and variation in evolutionary parameters. J. Evol. Biol. 29, 1882–1904 (2016).
Google Scholar
Duffy, G. A., Kuyucu, A. C., Hoskins, J. L., Hay, E. M. & Chown, S. L. Adequate sample sizes for improved accuracy of thermal trait estimates. Funct. Ecol. 35, 2647–2662 (2021).
Google Scholar
IUCN. The IUCN Red List of Threatened Species. https://www.iucnredlist.org (2021).
Harfoot, M. B. J. et al. Using the IUCN Red List to map threats to terrestrial vertebrates at global scale. Nat. Ecol. Evol. 5, 1510–1519 (2021).
Google Scholar
Sodhi, N. K. et al. Measuring the meltdown: Drivers of global amphibian extinction and decline. PLoS One 3 (2008).
Nowakowski, A. J. et al. Tropical amphibians in shifting thermal landscapes under land-use and climate change. Conserv. Physiol. 31, 96–105 (2017).
Jenkins, C. N., Pimm, S. L. & Joppa, L. N. Global patterns of terrestrial vertebrate diversity and conservation. Proc. Natl. Acad. Sci. USA 110, E2602–E2610 (2013).
Google Scholar
Ouzzani, M., Hammady, H., Fedorowicz, Z. & Elmagarmid, A. Rayyan—a web and mobile app for systematic reviews. Syst. Rev. 5, 210 (2016).
Google Scholar
Vera-Baceta, M.-A., Thelwall, M. & Kousha, K. Web of Science and Scopus language coverage. Scientometrics 121, 1803–1813 (2019).
Google Scholar
Giustini, D. & Boulos, M. N. K. Google Scholar is not enough to be used alone for systematic reviews. Online J. Public Health Inform. 5, 214 (2013).
Google Scholar
Haddaway, N. R., Collins, A. M., Coughlin, D. & Kirk, S. The role of Google Scholar in evidence reviews and its applicability to grey literature searching. PLoS One 10, e0138237 (2015).
Google Scholar
Gusenbauer, M. & Haddaway, N. R. Which academic search systems are suitable for systematic reviews or meta-analyses? Evaluating retrieval qualities of Google Scholar, PubMed, and 26 other resources. Res. Synth. Methods 11, 181–217 (2020).
Google Scholar
Harzing, A. Publish or perish. Res. Int. Manag. Softw. Release 27 (2007).
Cheng, C.-B. A study of warming tolerance and thermal acclimation capacity of tadpoles in Taiwan. (Tunghai University, 2017).
Wu, Q.-H. & Hsieh, C.-H. Thermal tolerance and population genetics of Hynobius fuca. (Chinese Culture University, 2016).
Jørgensen, L. B., Malte, H., Ørsted, M., Klahn, N. A. & Overgaard, J. A unifying model to estimate thermal tolerance limits in ectotherms across static, dynamic and fluctuating exposures to thermal stress. Sci. Rep. 11, 1–14 (2021).
Google Scholar
Agudelo-Cantero, G. A. & Navas, C. A. Interactive effects of experimental heating rates, ontogeny and body mass on the upper thermal limits of anuran larvae. J. Therm. Biol. 82, 43–51 (2019).
Google Scholar
Alveal Riquelme, N. Relaciones entre la fisiología térmica y las características bioclimáticas de Rhinella spinulosa (Anura: Bufonidae) en Chile a través del enlace mecanicista de nicho térmico. (Universidad de Concepción, 2015).
Alves, M. Tolerância térmica em espécies de anuros neotropicais do gênero Dendropsophus Fitzinger, 1843 e efeito da temperatura na resposta à predação. (Universidade Estadual de Santa Cruz, 2016).
Anderson, R. C. O. & Andrade, D. V. Trading heat and hops for water: Dehydration effects on locomotor performance, thermal limits, and thermoregulatory behavior of a terrestrial toad. Ecol. Evol. 7, 9066–9075 (2017).
Google Scholar
Aponte Gutiérrez, A. Endurecimiento térmico en Pristimantis medemi (Anura: Craugastoridae), en coberturas boscosas del Municipio de Villavicencio (Meta). (Universidad Nacional de Colombia, 2020).
Arrigada García, K. Conductas térmica en dos poblaciones de Batrachyla taeniata provenientes de la localidad de Ucúquer en la región de O’Higgins y de la localidad de Hualpén en la región del Bío-Bío (Universidad de Concepción, 2019).
Azambuja, G., Martins, I. K., Franco, J. L. & Santos, T. Gdos Effects of mancozeb on heat shock protein 70 (HSP70) and its relationship with the thermal physiology of Physalaemus henselii (Peters, 1872) tadpoles (Anura: Leptodactylidae). J. Therm. Biol. 98, 102911 (2021).
Google Scholar
Bacigalupe, L. D. et al. Natural selection on plasticity of thermal traits in a highly seasonal environment. Evol. Appl. 11, 2004–2013 (2018).
Google Scholar
Barria, A. M. & Bacigalupe, L. D. Intraspecific geographic variation in thermal limits and acclimatory capacity in a wide distributed endemic frog. J. Therm. Biol. 69, 254–260 (2017).
Google Scholar
Beltrán, I., Ramírez-Castañeda, V., Rodríguez-López, C., Lasso, E. & Amézquita, A. Dealing with hot rocky environments: critical thermal maxima and locomotor performance in Leptodactylus lithonaetes (anura: Leptodactylidae). Herpetol. J. 29, 155–161 (2019).
Google Scholar
Berkhouse, C. & Fries, J. Critical thermal maxima of juvenile and adult San Marcos salamanders (Eurycea nana). Southwest. Nat. 40, 430–434 (1995).
Blem, C. R., Ragan, C. A. & Scott, L. S. The thermal physiology of two sympatric treefrogs Hyla cinerea and Hyla chrysoscelis (Anura; Hylidae). Comp. Biochem. Physiol. 85, 563–570 (1986).
Google Scholar
Bonino, M. F., Cruz, F. B. & Perotti, M. G. Does temperature at local scale explain thermal biology patterns of temperate tadpoles? J. Therm. Biol. 94 (2020).
Bovo, R. P. Fisiologia térmica e balanço hídrico em anfíbios anuros. (Universidad Estadual Paulista, 2015).
Brattstrom, B. H. Thermal acclimation in Australian amphibians. Comp. Biochem. Physiol. 35, 69–103 (1970).
Google Scholar
Brattstrom, B. H. & Regal, P. Rate of thermal acclimation in the Mexican salamander. Chiropterotriton. Copeia 1965, 514–515 (1965).
Google Scholar
Brattstrom, B. H. A preliminary review of the thermal requirements of amphibians. Ecology 44, 238–255 (1963).
Google Scholar
Brattstrom, B. H. Thermal acclimation in anuran amphibians as a function of latitude and altitude. Comp. Biochem. Physiol. 24, 93–111 (1968).
Google Scholar
Brattstrom, B. H. & Lawrence, P. The rate of thermal acclimation in anuran amphibians. Physiol. Zool. 35, 148–156 (1962).
Google Scholar
Brown, H. A. The heat resistance of some anuran tadpoles (Hylidae and Pelobatidae). Copeia 1969, 138 (1969).
Google Scholar
Burke, E. M. & Pough, F. H. The role of fatigue in temperature resistance of salamanders. J. Therm. Biol. 1, 163–167 (1976).
Google Scholar
Burrowes, P. A., Navas, C. A., Jiménez-Robles, O., Delgado, P. & De La Riva, I. Climatic heterogeneity in the Bolivian andes: Are frogs trapped? S. Am. J. Herpetol. 18, 1–12 (2020).
Google Scholar
Bury, R. B. Low thermal tolerances of stream amphibians in the Pacific Northwest: Implications for riparian and forest management. Appl. Herpetol. 5, 63–74 (2008).
Google Scholar
Castellanos García, L. A. Days of futures past: Integrating physiology, microenvironments, and biogeographic history to predict response of frogs in neotropical dry-forest to global warming. (Universidad de los Andes, 2017).
Castro, B. Influence of environment on thermal ecology of direct-developing frogs (Anura: Craugastoridae: Pristimantis) in the eastern Andes of Colombia. (Universidad de los Andes, 2019).
Catenazzi, A., Lehr, E. & Vredenburg, V. T. Thermal physiology, disease, and amphibian declines on the eastern slopes of the Andes. Conserv. Biol. 28, 509–517 (2014).
Google Scholar
Chang, L.-W. Heat tolerance and its plasticity in larval Bufo bankorensis from different altitudes. (National Cheng Kung University, 2002).
Chavez Landi, P. A. Fisiología térmica de un depredador Dasythemis sp. (Odonata: Libellulidae) y su presa Hypsiboas pellucens (Anura: Hylidae) y sus posibles implicaciones frente al cambio climático. (Pontificia Universidad Católica Del Ecuador, 2017).
Chen, T.-C., Kam, Y.-C. & Lin, Y.-S. Thermal physiology and reproductive phenology of Buergeria japonica (Rhacophoridae) breeding in a stream and a geothermal hotspring in Taiwan. Zool. Sci. 18, 591–596 (2001).
Google Scholar
Cheng, Y.-J. Effect of salinity on the critical thermal maximum of tadpoles living in brackish water. (Tunghai University, 2017).
Christian, K. A., Nunez, F., Clos, L. & Diaz, L. Thermal relations of some tropical frogs along an altitudinal gradient. Biotropica 20, 236–239 (1988).
Google Scholar
Claussen, D. L. The thermal relations of the tailed frog, Ascaphus truei, and the pacific treefrog, Hyla regilla. Comp. Biochem. Physiol. 44, 137–153 (1973).
Google Scholar
Claussen, D. L. Thermal acclimation in ambystomatid salamanders. Comp. Biochem. Physiol. 58, 333–340 (1977).
Google Scholar
Contreras Cisneros, J. Temperatura crítica máxima, tolerancia al frío y termopreferendum del tritón del Montseny (Calotriton arnoldii). (Universitat de Barcelona, 2019).
Contreras Oñate, S. Posible efecto de las temperaturas de aclimatación sobre las respuestas térmicas en temperaturas críticas máximas (TCmás) y mínimas (TCmín) de una población de Batrachyla taeniata (Universidad de Concepción, 2016).
Cooper, R. D. & Shaffer, H. B. Allele-specific expression and gene regulation help explain transgressive thermal tolerance in non-native hybrids of the endangered California tiger salamander (Ambystoma californiense). Mol. Ecol. 30, 987–1004 (2021).
Google Scholar
Crow, J. C., Forstner, M. R. J., Ostr, K. G. & Tomasso, J. R. The role of temperature on survival and growth of the barton springs salamander (Eurycea sosorum). Herpetol. Conserv. Biol. 11, 328–334 (2016).
Cupp, P. V. Thermal tolerance of five salientian amphibians during development and metamorphosis. Herpetologica 36, 234–244 (1980).
Dabruzzi, T. F., Wygoda, M. L. & Bennett, W. A. Some like it hot: Heat tolerance of the crab-eating frog, Fejervarya cancrivora. Micronesica 43, 101–106 (2012).
Dainton, B. H. Heat tolerance and thyroid activity in developing tadpoles and juvenile adults of Xenopus laevis (Daudin). J. Therm. Biol. 16, 273–276 (1991).
Google Scholar
Daniel, N. J. J. Impact of climate change on Singapore amphibians. (National University of Singapore, 2013).
Davies, S. J., McGeoch, M. A. & Clusella-Trullas, S. Plasticity of thermal tolerance and metabolism but not water loss in an invasive reed frog. Comp. Biochem. Physiol. 189, 11–20 (2015).
Google Scholar
de Oliviera Anderson, R. C., Bovo, R. P. & Andrade, D. V. Seasonal variation in the thermal biology of a terrestrial toad, Rhinella icterica (Bufonidae), from the Brazilian Atlantic Forest. J. Therm. Biol. 74, 77–83 (2018).
Google Scholar
de Vlaming, V. L. & Bury, R. B. Thermal selection in tadpoles of the tailed-frog. Ascaphus truei. J. Herpetol. 4, 179–189 (1970).
Google Scholar
Delson, J. & Whitford, W. G. Critical thermal maxima in several life history stages in desert and montane populations of Ambystoma tigrinum. Herpetologica 29, 352–355 (1973).
Duarte, H. et al. Can amphibians take the heat? Vulnerability to climate warming in subtropical and temperate larval amphibian communities. Glob. Chang. Biol. 18, 412–421 (2012).
Google Scholar
Duarte, H. S. A comparative study of the thermal tolerance of tadpoles of Iberian anurans. (Universidade de Lisboa, 2011).
Dunlap, D. Evidence for a daily rhythm of heat resistance in cricket frogs, Acris crepitans. Copeia. 4, 852–854 (1969).
Google Scholar
Dunlap, D. G. Critical thermal maximum as a function of temperature of acclimation in two species of hylid frogs. Physiol. Zool. 41, 432–439 (1968).
Google Scholar
Elwood, J. R. L. Variation in hsp70 levels and thermotolerance among terrestrial salamanders of the Plethodon glutinosus complex. (Drexel University, 2003).
Enriquez-Urzelai, U. et al. Ontogenetic reduction in thermal tolerance is not alleviated by earlier developmental acclimation in Rana temporaria. Oecologia 189, 385–394 (2019).
Google Scholar
Enriquez-Urzelai, U. et al. The roles of acclimation and behaviour in buffering climate change impacts along elevational gradients. J. Anim. Ecol. 89, 1722–1734 (2020).
Google Scholar
Erskine, D. J. & Hutchison, V. H. Reduced thermal tolerance in an amphibian treated with melatonin. J. Therm. Biol. 7, 121–123 (1982).
Google Scholar
Escobar Serrano, D. Acclimation scope of the critical thermal limits in Agalychnis spurrelli (Hylidae) and Gastrotheca pseustes (Hemiphractidae) and their implications under climate change scenarios. (Pontificia Universidad Católica Del Ecuador, 2016).
Fan, X., Lei, H. & Lin, Z. Ontogenetic shifts in selected body temperature and thermal tolerance of the tiger frog. Hoplobatrachus chinensis. Acta Ecol. Sin. 32, 5574–5580 (2012).
Fan, X. L., Lin, Z. H. & Scheffers, B. R. Physiological, developmental, and behavioral plasticity in response to thermal acclimation. J. Therm. Biol. 97 (2021).
Fernández-Loras, A. et al. Infection with Batrachochytrium dendrobatidis lowers heat tolerance of tadpole hosts and cannot be cleared by brief exposure to CTmax. PLoS ONE 14 (2019).
Floyd, R. B. Ontogenetic change in the temperature tolerance of larval Bufo marinus (Anura: bufonidae). Comp. Biochem. Physiol. 75, 267–271 (1983).
Google Scholar
Floyd, R. B. Effects of photoperiod and starvation on the temperature tolerance of larvae of the giant toad, Bufo marinus. Copeia 1985, 625–631 (1985).
Google Scholar
Fong, S.-T. Thermal tolerance of adult Asiatic painted frog Kaloula pulchra from different populations. (National University of Tainan, 2014).
Frishkoff, L. O., Hadly, E. A. & Daily, G. C. Thermal niche predicts tolerance to habitat conversion in tropical amphibians and reptiles. Glob. Chang. Biol. 21, 3901–3916 (2015).
Google Scholar
Frost, J. S. & Martin, E. W. A comparison of distribution and high temperature tolerance in Bufo americanus and Bufo woodhousii fowleri. Copeia 1971, 750 (1971).
Google Scholar
Gatz, A. J. Critical thermal maxima of Ambystoma maculatum (Shaw) and Ambystoma jeffersonianum (Green) in relation to time of breeding. Herpetologica 27, 157–160 (1971).
Gatz, A. J. Intraspecific variations in critical thermal maxima of Ambystoma maculatum. Herpetologica 29, 264–268 (1973).
Geise, W. & Linsenmair, K. E. Adaptations of the reed frog Hyperolius viridiflavus (Amphibia, Anura, Hyperoliidae) to its arid environment – IV. Ecological significance of water economy with comments on thermoregulation and energy allocation. Oecologia 77, 327–338 (1988).
Google Scholar
González-del-Pliego, P. et al. Thermal tolerance and the importance of microhabitats for Andean frogs in the context of land use and climate change. J. Anim. Ecol. 89, 2451–2460 (2020).
Google Scholar
Gouveia, S. F. et al. Climatic niche at physiological and macroecological scales: The thermal tolerance-geographical range interface and niche dimensionality. Glob. Ecol. Biogeogr. 23, 446–456 (2014).
Google Scholar
Gray, R. Lack of physiological differentiation in three color morphs of the cricket frog (Acris crepitans) in Illinois. Trans. Ill. State Acad. Sci. 70, 73–79 (1977).
Google Scholar
Greenspan, S. E. et al. Infection increases vulnerability to climate change via effects on host thermal tolerance. Sci. Rep. 7 (2017).
Guevara-Molina, E. C., Gomes, F. R. & Camacho, A. Effects of dehydration on thermoregulatory behavior and thermal tolerance limits of Rana catesbeiana (Shaw, 1802). J. Therm. Biol. 93 (2020).
Gutiérrez Pesquera, L. Una valoración macrofisiológica de la vulnerabilidad al calentamiento global. Análisis de los límites de tolerancia térmica en comunidades de anfibios en gradients latitudinales y altitudinales. (Pontificia Universidad Católica Del Ecuador, 2015).
Gutiérrez Pesquera, M. Thermal tolerance across latitudinal and altitudinal gradients in tadpoles. (Universidad de Sevilla, 2016).
Gutiérrez-Pesquera, L. M. et al. Testing the climate variability hypothesis in thermal tolerance limits of tropical and temperate tadpoles. J. Biogeogr. 43, 1166–1178 (2016).
Google Scholar
Gvoždík, L., Puky, M. & Šugerková, M. Acclimation is beneficial at extreme test temperatures in the Danube crested newt, Triturus dobrogicus (Caudata, Salamandridae). Bio. J. Linn. Soc. 90, 627–636 (2007).
Google Scholar
Heatwole, H., De Austin, S. B. & Herrero, R. Heat tolerances of tadpoles of two species of tropical anurans. Comp. Biochem. Physiol. 27, 807–815 (1968).
Google Scholar
Heatwole, H., Mercado, N. & Ortiz, E. Comparison of critical thermal maxima of two species of Puerto Rican frogs of the genus. Eleutherodactylus. Physiol. Zool. 38, 1–8 (1965).
Google Scholar
Holzman, N. & McManus, J. J. Effects of acclimation on metabolic rate and thermal tolerance in the carpenter frog. Rana vergatipes. Comp. Biochem. Physiol. 45, 833–842 (1973).
Google Scholar
Hoppe, D. M. Thermal tolerance in tadpoles of the chorus frog Pseudacris triseriata. Herpetologica 34, 318–321 (1978).
Hou, P.-C. Thermal tolerance and preference in the adult amphibians from different altitudinal LTER sites. (National Cheng Kung University, 2003).
Howard, J. H., Wallace, R. L. & Stauffer, J. R. Jr Critical thermal maxima in populations of Ambystoma macrodactylum from different elevations. J. Herpetol. 17, 400–402 (1983).
Google Scholar
Hutchison, V. H. & Ritchart, J. P. Annual cycle of thermal tolerance in the salamander. Necturus maculosus. J. Herpetol. 23, 73–76 (1989).
Google Scholar
Hutchison, V. H. The distribution and ecology of the cave salamander, Eurycea lucifuga. Ecol. Monogr. 28, 2–20 (1958).
Google Scholar
Hutchison, V. H. Critical thermal maxima in salamanders. Physiol. Zool. 34, 92–125 (1961).
Google Scholar
Hutchison, V. H., Engbretson, G. & Turney, D. Thermal acclimation and tolerance in the hellbender, Cryptobranchus alleganiensis. Copeia 1973, 805–807 (1973).
Google Scholar
Hutchison, V. H. & Rowlan, S. D. Thermal acclimation and tolerance in the mudpuppy. Necturus maculosus. J. Herpetol. 9, 367–368 (1975).
Google Scholar
Jiang, S., Yu, P. & Hu, Q. A study on the critical thermal maxima of five species of salamanders of China. Acta Herpetol. Sin. 6, 56–62 (1987).
John-Alder, H. B., Morin, P. J. & Lawler, S. Thermal physiology, phenology, and distribution of tree frogs. Am. Nat. 132, 506–520 (1988).
Google Scholar
Johnson, C. R. Daily variation in the thermal tolerance of Litoria caerulea (Anura: Hylidae). Comp. Biochem. Physiol. 40, 1109–1111 (1971).
Google Scholar
Johnson, C. R. Thermal relations and water balance in the day frog, Taudactylus diurnus, from an Australian rain forest. Aust. J. Zool. 19, 35–39 (1971).
Google Scholar
Johnson, C. R. Diel variation in the thermal tolerance of Litoria gracilenta (Anura: Hylidae). Comp. Biochem. Physiol. 41, 727–730 (1972).
Google Scholar
Johnson, C. R. & Prine, J. E. The effects of sublethal concentrations of organophosphorus insecticides and an insect growth regulator on temperature tolerance in hydrated and dehydrated juvenile western toads. Bufo boreas. Comp. Biochem. Physiol. 53, 147–149 (1976).
Google Scholar
Johnson, C. R. Observations on body temperatures, critical thermal maxima and tolerance to water loss in the Australian hylid, Hyla caerulea (White). Proc. R. Soc. Qld. 82, 47–50 (1970).
Johnson, C. R. Thermal relations and daily variation in the thermal tolerance in. Bufo marinus. J. Herpetol. 6, 35 (1972).
Google Scholar
Johnson, C. Thermal relations in some southern and eastern Australian anurans. Proc. R. Soc. Qld. 82, 87–94 (1971).
Johnson, C. The effects of five organophosphorus insecticides on thermal stress in tadpoles of the Pacific tree frog. Hyla regilla. Zool. J. Linn. Soc. 69, 143–147 (1980).
Google Scholar
Katzenberger, M., Duarte, H., Relyea, R., Beltrán, J. F. & Tejedo, M. Variation in upper thermal tolerance among 19 species from temperate wetlands. J. Therm. Biol. 96 (2021).
Katzenberger, M. et al. Swimming with predators and pesticides: How environmental stressors affect the thermal physiology of tadpoles. PLoS ONE 9 (2014).
Katzenberger, M., Hammond, J., Tejedo, M. & Relyea, R. Source of environmental data and warming tolerance estimation in six species of North American larval anurans. J. Therm. Biol. 76, 171–178 (2018).
Google Scholar
Katzenberger, M. Thermal tolerance and sensitivity of amphibian larvae from Palearctic and Neotropical communities. (Universidade de Lisboa, 2013).
Katzenberger, M. Impact of global warming in holarctic and neotropical communities of amphibians. (Universidad de Sevilla, 2014).
Kern, P., Cramp, R. L. & Franklin, C. E. Temperature and UV-B-insensitive performance in tadpoles of the ornate burrowing frog: An ephemeral pond specialist. J. Exp. Biol. 217, 1246–1252 (2014).
Google Scholar
Kern, P., Cramp, R. L., Seebacher, F., Ghanizadeh Kazerouni, E. & Franklin, C. E. Plasticity of protective mechanisms only partially explains interactive effects of temperature and UVR on upper thermal limits. Comp. Biochem. Physiol. 190, 75–82 (2015).
Google Scholar
Kern, P., Cramp, R. L. & Franklin, C. E. Physiological responses of ectotherms to daily temperature variation. J. Exp. Biol. 218, 3068–3076 (2015).
Google Scholar
Komaki, S., Igawa, T., Lin, S.-M. & Sumida, M. Salinity and thermal tolerance of Japanese stream tree frog (Buergeria japonica) tadpoles from island populations. Herpetol. J. 26, 207–211 (2016).
Komaki, S., Lau, Q. & Igawa, T. Living in a Japanese onsen: Field observations and physiological measurements of hot spring amphibian tadpoles. Buergeria japonica. Amphib. Reptil. 37, 311–314 (2016).
Google Scholar
Krakauer, T. Tolerance limits of the toad, Bufo marinus, in South Florida. Comp. Biochem. Physiol. 33, 15–26 (1970).
Google Scholar
Kurabayashi, A. et al. Improved transport of the model amphibian, Xenopus tropicalis, and its viable temperature for transport. Curr. Herpetol. 33, 75–87 (2014).
Google Scholar
Lau, E. T. C., Leung, K. M. Y. & Karraker, N. E. Native amphibian larvae exhibit higher upper thermal limits but lower performance than their introduced predator. Gambusia affinis. J. Therm. Biol. 81, 154–161 (2019).
Google Scholar
Layne, J. R. & Claussen, D. L. Seasonal variation in the thermal acclimation of critical thermal maxima (CTMax) and minima (CTMin) in the salamander. Eurycea bislineata. J. Therm. Biol. 7, 29–33 (1982).
Google Scholar
Layne, J. R. & Claussen, D. L. The time courses of CTMax and CTMin acclimation in the salamander. Desmognathus fuscus. J. Therm. Biol. 7, 139–141 (1982).
Google Scholar
Lee, P.-T. Acidic effect on tadpoles living in container habitats. (Tunghai University, 2019).
Longhini, L. S., De Almeida Prado, C. P., Bícego, K. C., Zena, L. A. & Gargaglioni, L. H. Measuring cardiorespiratory variables on small tadpoles using a non-invasive methodology. Rev. Cuba. Investig. Biomed. 38 (2019).
López Rosero, A. C. Ontogenetic variation of thermal tolerance in two anuran species of Ecuador: Gastrotheca pseustes (Hemiphractidae) and Smilisca phaeota (Hylidae) and their relative vulnerability to environmental temperature change. (Pontificia Universidad Católica Del Ecuador, 2015).
Lotshaw, D. P. Temperature adaptation and effects of thermal acclimation in Rana sylvatica and Rana catesbeiana. Comp. Biochem. Physiol. 56, 287–294 (1977).
Google Scholar
Lu, H.-L., Wu, Q., Geng, J. & Dang, W. Swimming performance and thermal resistance of juvenile and adult newts acclimated to different temperatures. Acta Herpetol. 11, 189–195 (2016).
Lu, H. L., Geng, J., Xu, W., Ping, J. & Zhang, Y. P. Physiological response and changes in swimming performance after thermal acclimation in juvenile chinese fire-belly newts, Cynops orientalis. Acta Ecol. Sin. 37, 1603–1610 (2017).
Lutterschmidt, W. I. & Hutchison, V. H. The critical thermal maximum: Data to support the onset of spasms as the definitive end point. Can. J. Zool. 75, 1553–1560 (1997).
Google Scholar
Madalozzo, B. Variação latitudinal nos limites de tolerância e plasticidade térmica em anfíbios em um cenário de mudanças climáticas: efeito dos micro-habitats, sazonalidade e filogenia. (Universidade Federal de Santa Maria, 2018).
Mahoney, J. J. & Hutchison, V. H. Photoperiod acclimation and 24-hour variations in the critical thermal maxima of a tropical and a temperate frog. Oecologia 2, 143–161 (1969).
Google Scholar
Maness, J. D. & Hutchison, V. H. Acute adjustment of thermal tolerance in vertebrate ectotherms following exposure to critical thermal maxima. J. Therm. Biol. 5, 225–233 (1980).
Google Scholar
Manis, M. L. & Claussen, D. L. Environmental and genetic influences on the thermal physiology of Rana sylvatica. J. Therm. Biol. 11, 31–36 (1986).
Google Scholar
Markle, T. M. & Kozak, K. H. Low acclimation capacity of narrow-ranging thermal specialists exposes susceptibility to global climate change. Ecol. Evol. 8, 4644–4656 (2018).
Google Scholar
Marshall, E. & Grigg, G. C. Acclimation of CTM, LD50, and rapid loss of acclimation of thermal preferendum in tadpoles of Limnodynastes peronii (Anura, Myobatrachidae). Aust. Zool. 20, 447–456 (1980).
Mathias, J. H. The Comparative ecologies of two species of Amphibia (B. bufo and B. calamita) on the Ainsdale Sand Dunes National Nature Reserve. (The University of Manchester, 1971).
McManus, J. J. & Nellis, D. W. The critical thermal maximum of the marine toad, Bufo marinus. Caribb. J. Sci. 15, 67–70 (1975).
Menke, M. E. & Claussen, D. L. Thermal acclimation and hardening in tadpoles of the bullfrog, Rana catesbeiana. J. Therm. Biol. 7, 215–219 (1982).
Google Scholar
Merino-Viteri, A. R. The vulnerability of microhylid frogs, Cophixalus spp., to climate change in the Australian Wet Tropics. (James Cook University, 2018).
Messerman, A. F. Tales of an ‘invisible’ life stage: Survival and physiology among terrestrial juvenile ambystomatid salamanders. (University of Missouri, 2019).
Meza-Parral, Y., García-Robledo, C., Pineda, E., Escobar, F. & Donnelly, M. A. Standardized ethograms and a device for assessing amphibian thermal responses in a warming world. J. Therm. Biol. 89 (2020).
Miller, K. & Packard, G. C. Critical thermal maximum: Ecotypic variation between montane and piedmont chorus frogs (Pseudacris triseriata, Hylidae). Experientia 30, 355–356 (1974).
Google Scholar
Miller, K. & Packard, G. C. An altitudinal cline in critical thermal maxima of chorus frogs (Pseudacris triseriata). Am. Nat. 111, 267–277 (1977).
Google Scholar
Mueller, C. A., Bucsky, J., Korito, L. & Manzanares, S. Immediate and persistent effects of temperature on oxygen consumption and thermal tolerance in embryos and larvae of the baja California chorus frog, Pseudacris hypochondriaca. Front. Physiol. 10 (2019).
Navas, C. A., Antoniazzi, M. M., Carvalho, J. E., Suzuki, H. & Jared, C. Physiological basis for diurnal activity in dispersing juvenile Bufo granulosus in the Caatinga, a Brazilian semi-arid environment. Comp. Biochem. Physiol. 147, 647–657 (2007).
Google Scholar
Navas, C. A., Úbeda, C. A., Logares, R. & Jara, F. G. Thermal tolerances in tadpoles of three species of Patagonian anurans. S. Am. J. Herpetol. 5, 89–96 (2010).
Google Scholar
Nietfeldt, J. W., Jones, S. M., Droge, D. L. & Ballinger, R. E. Rate of thermal acclimation of larval Ambystoma tigrinum. J. Herpetol. 14, 209–211 (1980).
Google Scholar
Nol, R. & Ultsch, G. R. The roles of temperature and dissolved oxygen in microhabitat selection by the tadpoles of a frog (Rana pipiens) and a toad (Bufo terrestris). Copeia 1981, 645–652 (1981).
Google Scholar
Novarro, A. J. Thermal physiology in a widespread lungless salamander. (University of Maryland, 2018).
Nowakowski, A. J. et al. Thermal biology mediates responses of amphibians and reptiles to habitat modification. Ecol. Lett. 21, 345–355 (2018).
Google Scholar
Orille, A. C., McWhinnie, R. B., Brady, S. P. & Raffel, T. R. Positive effects of acclimation temperature on the critical thermal maxima of Ambystoma mexicanum and Xenopus laevis. J. Herpetol. 54, 289–292 (2020).
Google Scholar
Oyamaguchi, H. M. et al. Thermal sensitivity of a neotropical amphibian (Engystomops pustulosus) and its vulnerability to climate change. Biotropica 50, 326–337 (2018).
Google Scholar
Paez Vacas, M. I. Mechanisms of population divergence along elevational gradients in the tropics. (Colorado State University, 2016).
Paulson, B. K. & Hutchison, V. H. Blood changes in Bufo cognatus following acute heat stress. Comp. Biochem. Physiol. 87, 461–466 (1987).
Google Scholar
Paulson, B. & Hutchison, V. Origin of the stimulus for muscular spasms at the critical thermal maximum in anurans. Copeia 810–813 (1987).
Percino-Daniel, R. et al. Environmental heterogeneity shapes physiological traits in tropical direct-developing frogs. Ecol. Evol. (2021).
Perotti, M. G., Bonino, M. F., Ferraro, D. & Cruz, F. B. How sensitive are temperate tadpoles to climate change? The use of thermal physiology and niche model tools to assess vulnerability. Zoology 127, 95–105 (2018).
Google Scholar
Pintanel, P., Tejedo, M., Almeida-Reinoso, F., Merino-Viteri, A. & Gutiérrez-Pesquera, L. M. Critical thermal limits do not vary between wild-caught and captive-bred tadpoles of Agalychnis spurrelli (Anura: Hylidae). Diversity 12, 43 (2020).
Google Scholar
Pintanel, P., Tejedo, M., Ron, S. R., Llorente, G. A. & Merino-Viteri, A. Elevational and microclimatic drivers of thermal tolerance in Andean Pristimantis frogs. J. Biogeogr. 46, 1664–1675 (2019).
Google Scholar
Pintanel, P. Thermal adaptation of amphibians in tropical mountains. Consequences of global warming. (Universitat de Barcelona, 2018).
Pintanel, P., Tejedo, M., Salinas-Ivanenko, S., Jervis, P. & Merino-Viteri, A. Predators like it hot: Thermal mismatch in a predator-prey system across an elevational tropical gradient. J. Anim. Ecol. 90, 1985–1995 (2021).
Google Scholar
Pough, F. H. Natural daily temperature acclimation of eastern red efts, Notophthalmus v. viridescens (Rafinesque) (Amphibia: Caudata). Comp. Biochem. Physiol. 47, 71–78 (1974).
Google Scholar
Pough, F. H., Stewart, M. M. & Thomas, R. G. Physiological basis of habitat partitioning in Jamaican. Eleutherodactylus. Oecologia 27, 285–293 (1977).
Google Scholar
Quiroga, L. B., Sanabria, E. A., Fornés, M. W., Bustos, D. A. & Tejedo, M. Sublethal concentrations of chlorpyrifos induce changes in the thermal sensitivity and tolerance of anuran tadpoles in the toad Rhinella arenarum? Chemosphere 219, 671–677 (2019).
Google Scholar
Rausch, C. The thermal ecology of the red-spotted toad, Bufo punctatus, across life history. (University of Nevada, 2007).
Reichenbach, N. & Brophy, T. R. Natural history of the peaks of otter salamander (Plethodon hubrichti) along an elevational gradient. Herpetol. Bull. 141, 7–15 (2017).
Reider, K. E., Larson, D. J., Barnes, B. M. & Donnelly, M. A. Thermal adaptations to extreme freeze–thaw cycles in the high tropical Andes. Biotropica 53, 296–306 (2021).
Google Scholar
Richter-Boix, A. et al. Local divergence of thermal reaction norms among amphibian populations is affected by pond temperature variation. Evolution 69, 2210–2226 (2015).
Google Scholar
Riquelme, N. A., Díaz-Páez, H. & Ortiz, J. C. Thermal tolerance in the Andean toad Rhinella spinulosa (Anura: Bufonidae) at three sites located along a latitudinal gradient in Chile. J. Therm. Biol. 60, 237–245 (2016).
Google Scholar
Ritchart, J. P. & Hutchison, V. H. The effects of ATP and cAMP on the thermal tolerance of the mudpuppy. Necturus maculosus. J. Therm. Biol. 11, 47–51 (1986).
Google Scholar
Rivera-Burgos, A. C. Habitat suitability for Eleutherodactylus frogs in Puerto Rico: Indexing occupancy, abundance and reproduction to climatic and habitat characteristics. (North Carolina State University, 2019).
Rivera-Ordonez, J. M., Nowakowski, A. J., Manansala, A., Thompson, M. E. & Todd, B. D. Thermal niche variation among individuals of the poison frog, Oophaga pumilio, in forest and converted habitats. Biotropica 51, 747–756 (2019).
Google Scholar
Romero Barreto, P. Requerimientos fisiológicos y microambientales de dos especies de anfibios (Scinax ruber e Hyloxalus yasuni) del bosque tropical de Yasuní y sus implicaciones ante el cambio climático. (Pontificia Universidad Católica Del Ecuador, 2013).
Ruiz-Aravena, M. et al. Impact of global warming at the range margins: Phenotypic plasticity and behavioral thermoregulation will buffer an endemic amphibian. Ecol. Evol. 4, 4467–4475 (2014).
Google Scholar
Ruthsatz, K. et al. Thyroid hormone levels and temperature during development alter thermal tolerance and energetics of Xenopus laevis larvae. Conserv. Physiol. 6 (2018).
Ruthsatz, K. et al. Post-metamorphic carry-over effects of altered thyroid hormone level and developmental temperature: physiological plasticity and body condition at two life stages in Rana temporaria. J. Comp. Physiol. B: Biochem. Syst. Environ. Physiol. 190, 297–315 (2020).
Google Scholar
Rutledge, P. S., Spotila, J. R. & Easton, D. P. Heat hardening in response to two types of heat shock in the lungless salamanders Eurycea bislineata and Desmognathus ochrophaeus. J. Therm. Biol. 12, 235–241 (1987).
Google Scholar
Sanabria, E. et al. Effect of salinity on locomotor performance and thermal extremes of metamorphic Andean Toads (Rhinella spinulosa) from Monte Desert, Argentina. J. Therm. Biol. 74, 195–200 (2018).
Google Scholar
Sanabria, E. A., González, E., Quiroga, L. B. & Tejedo, M. Vulnerability to warming in a desert amphibian tadpole community: the role of interpopulational variation. J. Zool. 313, 283–296 (2021).
Google Scholar
Sanabria, E. A. & Quiroga, L. B. Change in the thermal biology of tadpoles of Odontophrynus occidentalis from the Monte desert, Argentina: Responses to photoperiod. J. Therm. Biol. 36, 288–291 (2011).
Google Scholar
Sanabria, E. A., Quiroga, L. B., González, E., Moreno, D. & Cataldo, A. Thermal parameters and locomotor performance in juvenile of Pleurodema nebulosum (Anura: Leptodactylidae) from the Monte Desert. J. Therm. Biol. 38, 390–395 (2013).
Google Scholar
Sanabria, E. A., Quiroga, L. B. & Martino, A. L. Seasonal changes in the thermal tolerances of the toad Rhinella arenarum (Bufonidae) in the Monte Desert of Argentina. J. Therm. Biol. 37, 409–412 (2012).
Google Scholar
Sanabria, E. A., Quiroga, L. B. & Martino, A. L. Seasonal Changes in the thermal tolerances of Odontophrynus occidentalis (Berg, 1896) (Anura: Cycloramphidae). Belg. J. Zool. 143, 23–29 (2013).
Sanabria, E. A. et al. Thermal ecology of the post-metamorphic Andean toad (Rhinella spinulosa) at elevation in the monte desert, Argentina. J. Therm. Biol. 52, 52–57 (2015).
Google Scholar
Sanabria, E. A., Vaira, M., Quiroga, L. B., Akmentins, M. S. & Pereyra, L. C. Variation of thermal parameters in two different color morphs of a diurnal poison toad, Melanophryniscus rubriventris (Anura: Bufonidae). J. Therm. Biol. 41, 1–5 (2014).
Google Scholar
Sanabria, E. A. & Quiroga, L. B. Thermal parameters changes in males of Rhinella arenarum (Anura: Bufonidae) related to reproductive periods. Rev. Biol. Trop. 59, 347–353 (2011).
Google Scholar
Scheffers, B. R. et al. Thermal buffering of microhabitats is a critical factor mediating warming vulnerability of frogs in the Philippine biodiversity hotspot. Biotropica 45, 628–635 (2013).
Google Scholar
Scheffers, B. R., Edwards, D. P., Diesmos, A., Williams, S. E. & Evans, T. A. Microhabitats reduce animal’s exposure to climate extremes. Glob. Chang. Biol. 20, 495–503 (2014).
Google Scholar
Schmid, W. D. High temperature tolerances of Bufo Hemiophrys and Bufo Cognatus. Ecology 46, 559–560 (1965).
Google Scholar
Sealander, J. A. & West, B. W. Critical thermal maxima of some Arkansas salamanders in relation to thermal acclimation. Herpetologica 25, 122–124 (1969).
Seibel, R. V. Variables affecting the critical thermal maximum of the leopard frog, Rana pipiens Schreber. Herpetologica 26, 208–213 (1970).
Sherman, E. Ontogenetic change in thermal tolerance of the toad Bufo woodhousii fowleri. Comp. Biochem. Physiol. 65, 227–230 (1980).
Google Scholar
Sherman, E. Thermal biology of newts (Notophthalmus viridescens) chronically infected with a naturally occurring pathogen. J. Therm. Biol. 33, 27–31 (2008).
Google Scholar
Sherman, E., Baldwin, L., Fernandez, G. & Deurell, E. Fever and thermal tolerance in the toad Bufo marinus. J. Therm. Biol. 16, 297–301 (1991).
Google Scholar
Sherman, E. & Levitis, D. Heat hardening as a function of developmental stage in larval and juvenile Bufo americanus and Xenopus laevis. J. Therm. Biol. 28, 373–380 (2003).
Google Scholar
Shi, L., Zhao, L., Ma, X. & Ma, X. Selected body temperature and thermal tolerance of tadpoles of two frog species (Fejervarya limnocharis and Microhyla ornata) acclimated under different thermal conditions. Acta Ecol. Sin. 32, 0465–0471 (2012).
Google Scholar
Simon, M. N., Ribeiro, P. L. & Navas, C. A. Upper thermal tolerance plasticity in tropical amphibian species from contrasting habitats: Implications for warming impact prediction. J. Therm. Biol. 48, 36–44 (2015).
Google Scholar
Simon, M. Plasticidade fenotípica em relação à temperatura de larvas de Rhinella (Anura: Bufonidae) da caatinga e da floresta Atlântica. (Universidade de Sao Paulo, 2010).
Skelly, D. K. & Freidenburg, L. K. Effects of beaver on the thermal biology of an amphibian. Ecol. Lett. 3, 483–486 (2000).
Google Scholar
Sos, T. Thermoconformity even in hot small temporary water bodies: a case study in yellow-bellied toad (Bombina v. variegata). Herpetol. Rom. 1, 1–11 (2007).
Spotila, J. R. Role of temperature and water in the ecology of lungless salamanders. Ecol. Monogr. 42, 95–125 (1972).
Google Scholar
Tracy, C. R., Christian, K. A., Betts, G. & Tracy, C. R. Body temperature and resistance to evaporative water loss in tropical Australian frogs. Comp. Biochem. Physiol. 150, 102–108 (2008).
Google Scholar
Turriago, J. L., Parra, C. A. & Bernal, M. H. Upper thermal tolerance in anuran embryos and tadpoles at constant and variable peak temperatures. Can. J. Zool. 93, 267–272 (2015).
Google Scholar
Vidal, M. A., Novoa-Muñoz, F., Werner, E., Torres, C. & Nova, R. Modeling warming predicts a physiological threshold for the extinction of the living fossil frog Calyptocephalella gayi. J. Therm. Biol. 69, 110–117 (2017).
Google Scholar
von May, R. et al. Divergence of thermal physiological traits in terrestrial breeding frogs along a tropical elevational gradient. Ecol. Evol. 7, 3257–3267 (2017).
Google Scholar
von May, R. et al. Thermal physiological traits in tropical lowland amphibians: Vulnerability to climate warming and cooling. PLoS ONE 14 (2019).
Wagener, C., Kruger, N. & Measey, J. Progeny of Xenopus laevis from altitudinal extremes display adaptive physiological performance. J. Exp. Biol. 224 (2021).
Wang, H. & Wang, L. Thermal adaptation of the common giant toad (Bufo gargarizans) at different earlier developmental stages. J. Agric. Univ. Hebei 31, 79–83 (2008).
Wang, L. The effects of constant and variable thermal acclimation on thermal tolerance of the common giant toad tadpoles (Bufo gargarizans). Acta Ecol. Sin. 34, 1030–1034 (2014).
Wang, L.-Z. & Li, X.-C. Effect of temperature on incubation and thermal tolerance of the Chinese forest frog. Chin. J. Zool. (2007).
Wang, L. & Li, X.-C. Effects of constant thermal acclimation on thermal tolerance of the Chinese forest frog (Rana chensineniss). Acta Hydrobiol. Sin. 31, 748–750 (2007).
Google Scholar
Wang, L.-Z., Li, X.-C. & Sun, T. Preferred temperature, avoidance temperature and lethal temperature of tadpoles of the common giant toad (Bufo gargarizans) and the Chinese forest frog (Rana chensinensis). Chin. J. Zool. 40, 23–27 (2005).
Warburg, M. R. On the water economy of Israel amphibians: The anurans. Comp. Biochem. Physiol. 40, 911–924 (1971).
Google Scholar
Warburg, M. R. The water economy of Israel amphibians: The urodeles Triturus vittatus (Jenyns) and Salamandra salamandra (L.). Comp. Biochem. Physiol. 40, 1055–1056, IN11,1057–1063 (1971).
Willhite, C. & Cupp, P. V. Daily rhythms of thermal tolerance in Rana clamitans (Anura: Ranidae) tadpoles. Comp. Biochem. Physiol. 72, 255–257 (1982).
Google Scholar
Wu, C.-S. & Kam, Y.-C. Thermal tolerance and thermoregulation by Taiwanese rhacophorid tadpoles (Buergeria japonica) living in geothermal hot springs and streams. Herpetologica 61, 35–46 (2005).
Google Scholar
Xu, X. The effect of temperature on body temperature and thermoregulation in different geographic populations of Rana dybowskii. (Harbin Normal University, 2017).
Yandún Vela, M. C. Capacidad de aclimatación en renacuajos de dos especies de anuros: Rhinella marina (Bufonidae) y Gastrotheca riobambae (Hemiphractidae) y su vulnerabilidad al cambio climático. (Pontificia Universidad Católica Del Ecuador, 2017).
Young, V. K. H. & Gifford, M. E. Limited capacity for acclimation of thermal physiology in a salamander. Desmognathus brimleyorum. J. Comp. Physiol. B: Biochem. Syst. Environ. Physiol. 183, 409–418 (2013).
Google Scholar
Yu, Z., Dickstein, R., Magee, W. E. & Spotila, J. R. Heat shock response in the salamanders Plethodon jordani and Plethodon cinereus. J. Therm. Biol. 23, 259–265 (1998).
Google Scholar
Zheng, R.-Q. & Liu, C.-T. Giant spiny-frog (Paa spinosa) from different populations differ in thermal preference but not in thermal tolerance. Aquat. Ecol. 44, 723–729 (2010).
Google Scholar
Zweifel, R. G. Studies on the critical thermal maxima of salamanders. Ecology 38, 64–69 (1957).
Google Scholar
Pick, J. L., Nakagawa, S. & Noble, D. W. A. Reproducible, flexible and high-throughput data extraction from primary literature: The metaDigitise r package. Methods Ecol. Evol. 10, 426–431 (2019).
Google Scholar
R Core Team. R: A language and environment for statistical computing.
Jetz, W. & Pyron, R. A. The interplay of past diversification and evolutionary isolation with present imperilment across the amphibian tree of life. Nat. Ecol. Evol. 2, 850–858 (2018).
Google Scholar
AmphibiaWeb. https://amphibiaweb.org. University of California, Berkeley, California, USA (2022).
Schwanz, L. E. et al. Best practices for building and curating databases for comparative analyses. J. Exp. Biol. 225, jeb243295 (2022).
Google Scholar
Pottier, P. et al. A comprehensive database of amphibian heat tolerance, Zenodo, https://doi.org/10.5281/zenodo.6565454 (2022).
Lajeunesse, M. J. Recovering Missing or Partial Data from Studies: A Survey of Conversions and Imputations for Meta-analysis. in Hanbook of Meta-analysis in Ecology and Evolution 195–206 (Princeton University Press, 2013).
Nakagawa, S., et al. A robust and readily implementable method for the meta-analysis of response ratios with and without missing standard deviations. EcoEvoRxiv, https://doi.org/10.32942/osf.io/7thx9 (2022)
Pottier, P., Burke, S., Drobniak, S. M., Lagisz, M. & Nakagawa, S. Sexual (in)equality? A meta-analysis of sex differences in thermal acclimation capacity across ectotherms. Funct. Ecol. 35, 2663–2678 (2021).
Google Scholar
Sunday, J. et al. Thermal tolerance patterns across latitude and elevation. Philos. Trans. R. Soc. B-Biol. Sci. 374, 20190036 (2019).
Google Scholar
Truebano, M., Fenner, P., Tills, O., Rundle, S. D. & Rezende, E. L. Thermal strategies vary with life history stage. J. Exp. Biol. 221, jeb171629 (2018).
Google Scholar
Rezende, E. L., Tejedo, M. & Santos, M. Estimating the adaptive potential of critical thermal limits: methodological problems and evolutionary implications. Funct. Ecol. 25, 111–121 (2011).
Google Scholar
Terblanche, J. S., Deere, J. A., Clusella-Trullas, S., Janion, C. & Chown, S. L. Critical thermal limits depend on methodological context. Proc. R. Soc. B-Biol. Sci. 274, 2935–2943 (2007).
Google Scholar
Hangartner, S., Sgrò, C. M., Connallon, T. & Booksmythe, I. Sexual dimorphism in phenotypic plasticity and persistence under environmental change: An extension of theory and meta-analysis of current data. Ecol. Lett. (2022).
Wickham, H. et al. Welcome to the tidyverse. J. Open Source Softw. 4, 1686 (2019).
Google Scholar
Dunnington, D. & Thorne, B. ggspatial: Spatial Data Framework for ggplot2. R package (2020).
Brownrigg, M. R. Package ‘maps’. R package (2013).
Yu, G., Smith, D. K., Zhu, H., Guan, Y. & Lam, T. T.-Y. ggtree: an R package for visualization and annotation of phylogenetic trees with their covariates and other associated data. Methods Ecol. Evol. 8, 28–36 (2017).
Google Scholar
Xu, S. et al. ggtreeExtra: Compact visualization of richly annotated phylogenetic data. Mol. Biol. Evol. 38, 4039–4042 (2021).
Google Scholar
Campitelli, E. ggnewscale: Multiple fill and colour scales in “ggplot2”. R package (2020).
Pedersen, T. L. patchwork: The Composer of Plots. R package (2020).
Paradis, E. & Schliep, K. ape 5.0: an environment for modern phylogenetics and evolutionary analyses in R. Bioinformatics 35, 526–528 (2019).
Google Scholar
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