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Australian Journal of Zoology Australian Journal of Zoology Society
Evolutionary, molecular and comparative zoology
RESEARCH ARTICLE

Thermal biology of the spotted snow skink, Niveoscincus ocellatus, along an altitudinal gradient

Luh P. E. K. Yuni A B , Susan M. Jones A and Erik Wapstra https://orcid.org/0000-0002-2050-8026 A C
+ Author Affiliations
- Author Affiliations

A School of Natural Sciences, University of Tasmania, Private Bag 55, Hobart, Tas. 7001, Australia.

B Program Study of Biology, Faculty of Mathematic and Natural Sciences, Udayana University, Bali 80361, Indonesia.

C Corresponding author. Email: erik.wapstra@utas.edu.au

Australian Journal of Zoology 66(4) 235-246 https://doi.org/10.1071/ZO18014
Submitted: 7 March 2018  Accepted: 29 January 2019   Published: 21 February 2019

Abstract

Body temperatures in ectotherms are strongly affected by their thermal environment. Ectotherms respond to variation in the thermal environment either by modification of behavioural thermoregulation to maintain their optimal body temperature or by shifting their optimal body temperature. In this study, the body temperatures of males of three populations of spotted snow skinks, Niveoscincus ocellatus, living along an altitudinal gradient (low, mid, and high altitude) were studied in the field and laboratory in spring, summer, and autumn, representing the full activity period of this species. The environmental variation across both sites and seasons affected their field active body temperatures. At the low and mid altitude, N. ocellatus had a higher mean body temperature than at the high altitude. Animals achieved their thermal preference at the low and mid altitude sites in all seasons. At the high altitude, however, N. ocellatus struggled to reach its preferred body temperatures, especially in autumn. The lower body temperature at the high-altitude site is likely due to limited thermal opportunity and/or an effect of avoiding the costs associated with increased intensity of basking.

Additional keywords: body temperature, climate change, lizards, thermal preference, thermoregulation.


References

Addo-Bediako, A., Chown, S. L., and Gaston, K. J. (2000). Thermal tolerance, climatic variability and latitude. Proceedings of the Royal Society of London, Series B: Biological Sciences 267, 739–745.
Thermal tolerance, climatic variability and latitude.Crossref | GoogleScholarGoogle Scholar |

Adolph, S. C., and Porter, W. L. (1993). Temperature, activity, and lizard life histories. American Naturalist 142, 273–295.
Temperature, activity, and lizard life histories.Crossref | GoogleScholarGoogle Scholar | 19425979PubMed |

Angilletta, M. J. (2009). ‘Thermal Adaptation: a Theoretical and Empirical Synthesis.’ (Oxford University Press: Oxford.)

Angilletta, M. J., Montgomery, L. G., and Werner, Y. L. (1999). Temperature preference in geckos: diel variation in juveniles and adults. Herpetologica 55, 212–222.

Angilletta, M. J., Niewiarowski, P. H., and Navas, C. A. (2002a). The evolution of thermal physiology in ectotherms. Journal of Thermal Biology 27, 249–268.
The evolution of thermal physiology in ectotherms.Crossref | GoogleScholarGoogle Scholar |

Angilletta, M. J., Hill, T., and Robson, M. A. (2002b). Is physiological performance optimized by thermoregulatory behaviour? A case study of the eastern fence lizard, Sceloporus undulatus. Journal of Thermal Biology 27, 199–204.
Is physiological performance optimized by thermoregulatory behaviour? A case study of the eastern fence lizard, Sceloporus undulatus.Crossref | GoogleScholarGoogle Scholar |

Araujo, M. B., Thuiller, W., and Pearson, R. G. (2006). Climate warming and the decline of amphibians and reptiles in Europe. Journal of Biogeography 33, 1712–1728.
Climate warming and the decline of amphibians and reptiles in Europe.Crossref | GoogleScholarGoogle Scholar |

Atkins, N., Swain, R., Wapstra, E., and Jones, S. M. (2007). Late stage deferral of parturition in the viviparous lizard Niveoscincus ocellatus (Gray 1845): implications for offspring quality and survival. Biological Journal of the Linnean Society 90, 735–746.
Late stage deferral of parturition in the viviparous lizard Niveoscincus ocellatus (Gray 1845): implications for offspring quality and survival.Crossref | GoogleScholarGoogle Scholar |

Beck, D. D., and Lowe, C. H. (1994). Resting metabolism of helodermatid lizards: allometric and ecological relationship. Journal of Comparative Physiology B: Biochemical, Systemic, and Environmental Physiology 164, 124–129.
Resting metabolism of helodermatid lizards: allometric and ecological relationship.Crossref | GoogleScholarGoogle Scholar |

Beldade, P., Mateus, A. A., and Keller, R. A. (2011). Evolution and molecular mechanisms of adaptive developmental plasticity. Molecular Ecology 20, 1347–1363.
Evolution and molecular mechanisms of adaptive developmental plasticity.Crossref | GoogleScholarGoogle Scholar | 21342300PubMed |

Besson, A. A., and Cree, A. (2010). A cold-adapted reptile becomes a more effective thermoregulator in a thermally challenging environment. Oecologia 163, 571–581.
A cold-adapted reptile becomes a more effective thermoregulator in a thermally challenging environment.Crossref | GoogleScholarGoogle Scholar | 20140685PubMed |

Bonebrake, T. C., Brown, C. J., Bell, J. D., Blanchard, J. L., Chauvenet, A., Champion, C., Chen, I., Clark, T. D., Colwell, R. K., Danielsen, F., Dell, A. I., Donelson, J. M., Evengard, B., Ferrier, S., Frusher, S., Garcia, R. A., Griffis, R. B., Hobday, A. J., Jarzyna, M. A., Lee, E., Lenoir, J., Linnetved, H., Martin, V. Y., McCormack, P. C., McDonald, J., McDonald-Madden, E., Mitchell, N., Mustonen, T., Pandolfi, J. M., Pettorelli, N., Possingham, H., Pulsifer, P., Reynolds, M., Scheffers, B. R., Sorte, C. J. B., Strugnell, J. M., Tuanmu, M., Twiname, S., Vergés, A., Villanueva, A., Wapstra, E., Wernberg, T., and Pecl, G. T. (2018). Managing consequences of climate-driven species redistribution requires integration of ecology, conservation and social science. Biological Reviews of the Cambridge Philosophical Society 93, 284–305.
Managing consequences of climate-driven species redistribution requires integration of ecology, conservation and social science.Crossref | GoogleScholarGoogle Scholar | 28568902PubMed |

Bonino, M. F., Azocar, D. L. M., Tulli, M. J., Abdala, C. S., Perotti, M. G., and Cruz, F. B. (2011). Running in cold weather: morphology, thermal biology, and performance in the southernmost lizard clade in the world (Liolaemus lineomaculatus section: Liolaemini: Iguina). The Journal of Experimental Zoology 315A, 495–503.
Running in cold weather: morphology, thermal biology, and performance in the southernmost lizard clade in the world (Liolaemus lineomaculatus section: Liolaemini: Iguina).Crossref | GoogleScholarGoogle Scholar |

Bureau of Meteorology Australia (2019). Monthly mean maximum and minimum air temperature (2001–2010). Available at: http://www.bom.gov.au/ [accessed 17 May 2014].

Cadby, C. D., While, G. M., Hobday, A. J., Uller, T., and Wapstra, E. (2010). Multi-scale approach to understanding climate effects on offspring size at birth and date of birth in a reptile. Integrative Zoology 5, 164–175.
Multi-scale approach to understanding climate effects on offspring size at birth and date of birth in a reptile.Crossref | GoogleScholarGoogle Scholar | 21392334PubMed |

Cadby, C. D., Jones, S. M., and Wapstra, E. (2014). Geographical differences in maternal basking behaviour and offspring growth rate in a climatically widespread viviparous reptile. The Journal of Experimental Biology 217, 1175–1179.
Geographical differences in maternal basking behaviour and offspring growth rate in a climatically widespread viviparous reptile.Crossref | GoogleScholarGoogle Scholar | 24311810PubMed |

Caldwell, A. J., While, G. M., Beeton, N., and Wapstra, E. (2015). Potential for thermal tolerance to mediate climate change effects on three members of a cool temperate lizard genus, Niveoscincus. Journal of Thermal Biology 52, 14–23.
Potential for thermal tolerance to mediate climate change effects on three members of a cool temperate lizard genus, Niveoscincus.Crossref | GoogleScholarGoogle Scholar | 26267494PubMed |

Caldwell, A. J., While, G. M., and Wapstra, E. (2017). Plasticity of thermoregulatory behaviour in response to the thermal environment: a comparative test across specialist and generalist reptile species. Animal Behaviour 132, 217–227.
Plasticity of thermoregulatory behaviour in response to the thermal environment: a comparative test across specialist and generalist reptile species.Crossref | GoogleScholarGoogle Scholar |

Castaneda, L. E., Lardies, M. A., and Bozinovic, F. (2004). Adaptive latitudinal shifts in the thermal physiology of a terrestrial isopod. Evolutionary Ecology Research 6, 579–593.

Ceia-Hasse, A., Sinervo, B., Vicente, L., and Pereira, H. H. (2014). Integrating ecophysiological models into species distribution projections of European reptile range shifts in response to climate change. Ecography 37, 679–688.
Integrating ecophysiological models into species distribution projections of European reptile range shifts in response to climate change.Crossref | GoogleScholarGoogle Scholar |

Chamaille-Jammes, S., Massot, M., Aragon, P., and Clobert, J. (2006). Global warming and positive fitness response in mountain populations of common lizards Lacerta vivipara. Global Change Biology 12, 392–402.
Global warming and positive fitness response in mountain populations of common lizards Lacerta vivipara.Crossref | GoogleScholarGoogle Scholar |

Christian, K. A., and Bedford, G. (1995). Seasonal changes in thermoregulation by the frillneck lizard, Chlamydosaurus kingii in tropical Australia. Ecology 76, 124–132.
Seasonal changes in thermoregulation by the frillneck lizard, Chlamydosaurus kingii in tropical Australia.Crossref | GoogleScholarGoogle Scholar |

Christian, K., and Bedford, G. S. (1996). Thermoregulation by the spotted tree monitor, Varanus scalaris, in the seasonal tropics of Australia. Journal of Thermal Biology 21, 67–73.
Thermoregulation by the spotted tree monitor, Varanus scalaris, in the seasonal tropics of Australia.Crossref | GoogleScholarGoogle Scholar |

Christian, K. A., and Weavers, B. (1996). Thermoregulation of monitor lizards in Australia: an evaluation of methods in thermal biology. Ecological Monographs 66, 139–157.
Thermoregulation of monitor lizards in Australia: an evaluation of methods in thermal biology.Crossref | GoogleScholarGoogle Scholar |

Christian, K. A., Bedford, G., Green, B., Schultz, T., and Newgrain, K. (1998). Energetics and water flux of the marbled velvet gecko in tropical and temperate habitats. Oecologia 116, 336–342.
Energetics and water flux of the marbled velvet gecko in tropical and temperate habitats.Crossref | GoogleScholarGoogle Scholar | 28308064PubMed |

Christian, K. A., Webb, J. K., Schultz, T. J., and Green, B. (2007). Effects of seasonal variation in prey abundance on field metabolism, water flux, and activity of a tropical ambush foraging snake. Physiological and Biochemical Zoology 80, 522–533.
Effects of seasonal variation in prey abundance on field metabolism, water flux, and activity of a tropical ambush foraging snake.Crossref | GoogleScholarGoogle Scholar |

Christian, K. A., Tracy, C. R., and Tracy, C. R. (2016). Body temperatures and the thermal environment. In ‘Reptile Ecology and Conservation: A Handbook of Techniques’. (Ed. C. K. Dodd, Jr.) pp. 337–351. (Oxford University Press.)

Clarke, A. (1993). Seasonal acclimatization and latitudinal compensation in metabolism: do they exist? Functional Ecology 7, 139–149.
Seasonal acclimatization and latitudinal compensation in metabolism: do they exist?Crossref | GoogleScholarGoogle Scholar |

Cliff, H. B., Wapstra, E., and Burridge, C. P. (2015). Persistence and dispersal in a Southern Hemisphere glaciated landscape: the phylogeography of the spotted snow skink (Niveoscincus ocellatus) in Tasmania. BMC Evolutionary Biology 15, 121.
Persistence and dispersal in a Southern Hemisphere glaciated landscape: the phylogeography of the spotted snow skink (Niveoscincus ocellatus) in Tasmania.Crossref | GoogleScholarGoogle Scholar | 26111715PubMed |

Climate Futures for Tasmania (2010). General climate impacts technical report. The Antarctic Climate and Ecosystem Research Centre, Tasmania.

Clusella-Trullas, S., and Chown, S. L. (2014). Lizard thermal trait variation at multiple scales: a review. Journal of Comparative Physiology B: Biochemical, Systemic, and Environmental Physiology 184, 5–21.
Lizard thermal trait variation at multiple scales: a review.Crossref | GoogleScholarGoogle Scholar | 23989339PubMed |

Clusella-Trullas, S., Terblanche, J. S., van Wyx, J. H., and Spotila, J. R. (2007). Low repeatability of preferred body temperature in four species of cordylid lizards: temporal variation and implications for adaptive significance. Evolutionary Ecology 21, 63–79.
Low repeatability of preferred body temperature in four species of cordylid lizards: temporal variation and implications for adaptive significance.Crossref | GoogleScholarGoogle Scholar |

Clusella-Trullas, S., Blackburn, T. M., and Chown, S. L. (2011). Climatic predictors of temperature performance curve in ectotherms imply complex response to climate change. American Naturalist 177, 738–751.
Climatic predictors of temperature performance curve in ectotherms imply complex response to climate change.Crossref | GoogleScholarGoogle Scholar | 21597251PubMed |

Cunningham, G., While, G., and Wapstra, E. (2017). Climate and sex ratio variation in a viviparous lizard. Biology Letters 13, 20170218.
Climate and sex ratio variation in a viviparous lizard.Crossref | GoogleScholarGoogle Scholar | 28566543PubMed |

Cunningham, G. D., Fitzpatrick, L. J., While, G. M., and Wapstra, E. (2018). Plastic rates of development and the effect of thermal extremes on offspring fitness in a cold-climate viviparous lizard. Journal of Experimental Zoology A 329, 262–270.
Plastic rates of development and the effect of thermal extremes on offspring fitness in a cold-climate viviparous lizard.Crossref | GoogleScholarGoogle Scholar |

Diaz, J. A., and Cabezas-Diaz, S. (2004). Seasonal variation in the contribution of different behavioural mechanisms to lizard thermoregulation. Functional Ecology 18, 867–875.
Seasonal variation in the contribution of different behavioural mechanisms to lizard thermoregulation.Crossref | GoogleScholarGoogle Scholar |

Diaz, J. A., Iraeta, P., and Monasterio, C. (2006). Seasonality provokes a shift of thermal preferences in a temperate lizard, but altitude does not. Journal of Thermal Biology 31, 237–242.
Seasonality provokes a shift of thermal preferences in a temperate lizard, but altitude does not.Crossref | GoogleScholarGoogle Scholar |

Grant, B. W., and Dunham, A. E. (1990). Elevational covariation in environmental constraints and life histories of the desert lizard Sceloporus merriami. Ecology 71, 1765–1776.
Elevational covariation in environmental constraints and life histories of the desert lizard Sceloporus merriami.Crossref | GoogleScholarGoogle Scholar |

Gutierrez, J. A., Krenz, J. D., and Ibarguengoytia, N. R. (2010). Effect of altitude on thermal responses of Liolaemus pictus argentinus in Argentina. Journal of Thermal Biology 35, 332–337.
Effect of altitude on thermal responses of Liolaemus pictus argentinus in Argentina.Crossref | GoogleScholarGoogle Scholar |

Gvozdik, L., and Castilla, A. M. (2001). A comparative study of preferred body temperatures and critical thermal tolerance limits among populations of Zootoca vivipara (Squamata: Lacertidae) along an altitudinal gradient. Journal of Herpetology 35, 486–492.
A comparative study of preferred body temperatures and critical thermal tolerance limits among populations of Zootoca vivipara (Squamata: Lacertidae) along an altitudinal gradient.Crossref | GoogleScholarGoogle Scholar |

Hadamova, M., and Gvozdik, L. (2011). Seasonal acclimation of preferred body temperatures improves the opportunity for thermoregulation in newts. Physiological and Biochemical Zoology 84, 166–174.
Seasonal acclimation of preferred body temperatures improves the opportunity for thermoregulation in newts.Crossref | GoogleScholarGoogle Scholar | 21460527PubMed |

Hertz, P. E., and Huey, R. B. (1981). Compensation for altitudinal changes in the thermal environment by some Anolis lizards on Hispaniola. Ecology 62, 515–521.
Compensation for altitudinal changes in the thermal environment by some Anolis lizards on Hispaniola.Crossref | GoogleScholarGoogle Scholar |

Hertz, P. E., Huey, R. B., and Nevo, E. (1983). Homage to Santa Anita: thermal sensitivity of sprint speed in agamid lizards. Evolution 37, 1075–1084.
Homage to Santa Anita: thermal sensitivity of sprint speed in agamid lizards.Crossref | GoogleScholarGoogle Scholar | 28563551PubMed |

Hertz, P. E., Huey, R. B., and Stevenson, R. D. (1993). Evaluating temperature regulation by field-active ectotherms: the fallacy of the inappropriate question. American Naturalist 142, 796–818.
Evaluating temperature regulation by field-active ectotherms: the fallacy of the inappropriate question.Crossref | GoogleScholarGoogle Scholar | 19425957PubMed |

Huang, S., and Tu, M. (2009). Locomotor and elevational distribution of a mountainous lizard, Takydromus hsuehshanensis, in Taiwan. Zoological Studies (Taipei, Taiwan) 48, 477–484.

Huey, R. B., and Bennett, A. F. (1990). Physiological adjustments to fluctuating thermal environments: an ecological and evolutionary perspective. In ‘The Role of Heat Shock and Stress Response in Biology and Human Disease’. (Eds R. Morimoto, A. Tissieres, and C. Georgopoulous.) pp. 37–59. (Cold Spring Harbor Laboratory Press.)

Huey, R. B., and Slatkin, M. (1976). Cost and benefits of lizard thermoregulation. The Quarterly Review of Biology 51, 363–384.
Cost and benefits of lizard thermoregulation.Crossref | GoogleScholarGoogle Scholar | 981504PubMed |

Huey, R. B., Kearney, M. R., Krockenberger, A., Holtum, J. A. M., Jess, M., and Williams, S. E. (2012). Predicting organismal vulnerability to climate warming: roles of behavior, physiology and adaptation. Philosophical Transactions of the Royal Society of London Series B: Biological Sciences 367, 1665–1679.
Predicting organismal vulnerability to climate warming: roles of behavior, physiology and adaptation.Crossref | GoogleScholarGoogle Scholar | 22566674PubMed |

Ibarguengoytia, N. R., Medina, S. M., Fernandez, J. B., Gutierrez, J. A., Tappari, F., and Scolaro, A. (2010). Thermal biology of the southernmost lizards in the world: Liolaemus sarmientoi and Liolaemus magellanicus from Patagonia, Argentina. Journal of Thermal Biology 35, 21–27.
Thermal biology of the southernmost lizards in the world: Liolaemus sarmientoi and Liolaemus magellanicus from Patagonia, Argentina.Crossref | GoogleScholarGoogle Scholar |

Janzen, D. H. (1967). Why mountain passes are higher in the tropics. American Naturalist 101, 233–249.
Why mountain passes are higher in the tropics.Crossref | GoogleScholarGoogle Scholar |

Kearney, M., Shine, R., and Porter, W. P. (2009). The potential for behavioral thermoregulation to buffer “cold-blooded” animals against climate warming. Proceedings of the National Academy of Sciences of the United States of America 106, 3835–3840.
The potential for behavioral thermoregulation to buffer “cold-blooded” animals against climate warming.Crossref | GoogleScholarGoogle Scholar | 19234117PubMed |

Kearney, M. R., Simpson, S. J., Raubenheimer, D., and Kooijman, S. A. L. M. (2013). Balancing heat, water and nutrients, under environmental change: a thermodynamic niche framework. Functional Ecology 27, 950–966.
Balancing heat, water and nutrients, under environmental change: a thermodynamic niche framework.Crossref | GoogleScholarGoogle Scholar |

Kohlsdorf, T., and Navas, C. A. (2006). Ecological constraints on the evolutionary association between field and preferred temperatures in Tropidurinae lizards. Evolutionary Ecology 20, 549–564.
Ecological constraints on the evolutionary association between field and preferred temperatures in Tropidurinae lizards.Crossref | GoogleScholarGoogle Scholar |

Kubisch, E. L., Fernandez, J. H., and Ibarguengoytia, N. R. (2011). Is locomotor performance optimised at preferred body temperature? A study of Liolaemus pictus argentinus from northern Patagonia, Argentina. Journal of Thermal Biology 36, 328–333.
Is locomotor performance optimised at preferred body temperature? A study of Liolaemus pictus argentinus from northern Patagonia, Argentina.Crossref | GoogleScholarGoogle Scholar |

Lin, C., Zhang, L., and Ji, X. (2008). Influence of pregnancy on locomotor and feeding performances of the skink, Mabuya multifasciata: why do females shift thermal preferences when pregnant? Zoology 111, 188–195.
Influence of pregnancy on locomotor and feeding performances of the skink, Mabuya multifasciata: why do females shift thermal preferences when pregnant?Crossref | GoogleScholarGoogle Scholar | 18262397PubMed |

Lourdais, O., Guillon, M., DeNardo, D., and Blouin-Demers, G. (2013). Cold climate specialization: adaptive covariation between metabolic rate and thermoregulation in pregnant vipers. Physiology & Behavior 119, 149–155.
Cold climate specialization: adaptive covariation between metabolic rate and thermoregulation in pregnant vipers.Crossref | GoogleScholarGoogle Scholar |

Martins, L. S., Verrastro, L., and Tozetti, A. M. (2014). The influences of habitat on body temperature control in a southern population of Liolaemus occipitalis (Boulenger, 1885) in Brazil. South American Journal of Herpetology 9, 9–13.
The influences of habitat on body temperature control in a southern population of Liolaemus occipitalis (Boulenger, 1885) in Brazil.Crossref | GoogleScholarGoogle Scholar |

Mathies, T., and Andrews, R. M. (1997). Influence of pregnancy on the thermal biology of the lizard, Sceloporus jarrovi: why do pregnant females exhibit low body temperatures? Functional Ecology 11, 498–507.
Influence of pregnancy on the thermal biology of the lizard, Sceloporus jarrovi: why do pregnant females exhibit low body temperatures?Crossref | GoogleScholarGoogle Scholar |

McConnachie, S., Alexander, G. J., and Whiting, M. J. (2009). Selected body temperature and thermoregulatory behavior in the sit-and-wait foraging lizard Pseudocordylus melanotus melanotus. Herpetological Monograph 23, 108–122.
Selected body temperature and thermoregulatory behavior in the sit-and-wait foraging lizard Pseudocordylus melanotus melanotus.Crossref | GoogleScholarGoogle Scholar |

Melville, J. (2007). Evolutionary correlations between microhabitat specialization and locomotor capabilities in the lizard genus Niveoscincus. Australian Journal of Zoology 55, 351–355.
Evolutionary correlations between microhabitat specialization and locomotor capabilities in the lizard genus Niveoscincus.Crossref | GoogleScholarGoogle Scholar |

Melville, J., and Swain, R. (2003). Evolutionary correlations between escape behaviour and performance ability in eight species of snow skinks (Niveoscincus: Lygosominae) from Tasmania. Journal of Zoology 261, 79–89.
Evolutionary correlations between escape behaviour and performance ability in eight species of snow skinks (Niveoscincus: Lygosominae) from Tasmania.Crossref | GoogleScholarGoogle Scholar |

Miles, D. B. (1994). Population differentiation in locomotor performance and the potential response of a terrestrial organism to global environmental change. American Zoologist 34, 422–436.
Population differentiation in locomotor performance and the potential response of a terrestrial organism to global environmental change.Crossref | GoogleScholarGoogle Scholar |

Muschett, G., Umbers, K. D. L., and Herberstein, M. E. (2017). Within-season variability of fighting behavior in an Australian alpine grasshopper. PLoS ONE 12, e0171697.
Within-season variability of fighting behavior in an Australian alpine grasshopper.Crossref | GoogleScholarGoogle Scholar | 28403243PubMed |

Nelson, L. S., and Cooper, P. D. (2017). Seasonal effects on body temperature of the endangered grassland earless dragon, Tympanocryptus pinguicolla, from populations at two elevations. Australian Journal of Zoology 65, 165–178.
Seasonal effects on body temperature of the endangered grassland earless dragon, Tympanocryptus pinguicolla, from populations at two elevations.Crossref | GoogleScholarGoogle Scholar |

Ortega, Z., Perez-Mellado, V., Garrido, M., Guerra, C., Villa-Garcia, A., and Alonso-Fernandez, T. (2014). Seasonal changes in thermal biology of Podarcis lilfordi (Squamata, Lacertidae) consistently depend on habitat traits. Journal of Thermal Biology 39, 32–39.
Seasonal changes in thermal biology of Podarcis lilfordi (Squamata, Lacertidae) consistently depend on habitat traits.Crossref | GoogleScholarGoogle Scholar |

Peck, L. S., Clark, M. S., Morley, S. A., Massey, A., and Rossetti, H. (2009). Animal temperature limits and ecological relevance: effects of size, activity and rates of change. Functional Ecology 23, 248–256.
Animal temperature limits and ecological relevance: effects of size, activity and rates of change.Crossref | GoogleScholarGoogle Scholar |

Pen, I., Uller, T., Feldmeyer, B., Harts, A., While, G. M., and Wapstra, E. (2010). Climate-driven population in sex-determining systems. Nature 468, 436–438.
Climate-driven population in sex-determining systems.Crossref | GoogleScholarGoogle Scholar | 20981009PubMed |

Phillips, B. L., Munoz, M. M., Hatcher, A., Macdonald, S. L., Llewelyn, J., Lucy, V., and Moritz, C. (2016). Heat hardening in a tropical lizard: geographic variation explained by the predictability and variance in environmental temperatures. Functional Ecology 30, 1161–1168.
Heat hardening in a tropical lizard: geographic variation explained by the predictability and variance in environmental temperatures.Crossref | GoogleScholarGoogle Scholar |

Pörtner, H. O., and Farrell, A. P. (2008). Physiology and climate change. Science 322, 690–692.
Physiology and climate change.Crossref | GoogleScholarGoogle Scholar | 18974339PubMed |

Reside, A. E., Welbergen, J. A., Phillips, B. L., Wardell-Johnson, G. W., Keppel, G., Ferrier, S., Williams, S. E., and Vanderwal, J. (2014). Characteristics of climate change refugia for Australian biodiversity. Austral Ecology 39, 887–897.
Characteristics of climate change refugia for Australian biodiversity.Crossref | GoogleScholarGoogle Scholar |

Schaefer, J., and Walters, A. (2010). Metabolic cold adaptation and developmental plasticity in metabolic rates among species in the Fundulus notatus species complex. Functional Ecology 24, 1087–1094.
Metabolic cold adaptation and developmental plasticity in metabolic rates among species in the Fundulus notatus species complex.Crossref | GoogleScholarGoogle Scholar |

Scheers, H., and Van Damme, R. (2002). Micro-scale differences in thermal quality and a possible case of evolutionary flexibility in the thermal physiology of lacertid lizards. Oecologia 132, 323–331.
Micro-scale differences in thermal quality and a possible case of evolutionary flexibility in the thermal physiology of lacertid lizards.Crossref | GoogleScholarGoogle Scholar | 28547409PubMed |

Scheffer, M., Vergnon, R., Cornelissen, J. H. C., Hantson, S., Holmgren, M., van Nes, E. H., and Xu, C. (2014). Why trees and shrubs but rarely trubs? Trends in Ecology & Evolution 29, 433–434.
Why trees and shrubs but rarely trubs?Crossref | GoogleScholarGoogle Scholar |

Sears, M. W., and Angilletta, M. J. (2003). Life-history variation in the sagebrush lizard: phenotypic plasticity or local adaptation. Ecology 84, 1624–1634.
Life-history variation in the sagebrush lizard: phenotypic plasticity or local adaptation.Crossref | GoogleScholarGoogle Scholar |

Seebacher, F. (2005). A review of thermoregulation and physiological performance in reptiles: what is the role of phenotypic flexibility? Journal of Comparative Physiology B: Biochemical, Systemic, and Environmental Physiology 175, 453–461.
A review of thermoregulation and physiological performance in reptiles: what is the role of phenotypic flexibility?Crossref | GoogleScholarGoogle Scholar | 16034580PubMed |

Seebacher, F. (2009). Responses to temperature variation: integration of thermoregulation and metabolism in vertebrates. The Journal of Experimental Biology 212, 2885–2891.
Responses to temperature variation: integration of thermoregulation and metabolism in vertebrates.Crossref | GoogleScholarGoogle Scholar | 19717669PubMed |

Seebacher, F., Holmes, S., Roosen, N. J., Nouvian, M., Wilson, R. S., and Ward, A. J. W. (2012). Capacity for thermal acclimation differs between populations and phylogenetic lineages within a species. Functional Ecology 26, 1418–1428.
Capacity for thermal acclimation differs between populations and phylogenetic lineages within a species.Crossref | GoogleScholarGoogle Scholar |

Sepulveda, M., Vidal, M. A., Farina, J. M., and Sabat, P. (2008). Seasonal and geographic variation in thermal biology of the lizard Microlophus atacamensis (Squamata: Tropiduradae). Journal of Thermal Biology 33, 141–148.
Seasonal and geographic variation in thermal biology of the lizard Microlophus atacamensis (Squamata: Tropiduradae).Crossref | GoogleScholarGoogle Scholar |

Sinervo, B., Mendez-de-la-Cruz, F, Miles, D. B., Heulin, B, Bastiaans, E, Villagran-Santa Cruz, M, Lara-Resendiz, R, Martinez-Mendez, N, Calderon-Espinosa, M. L., Meza-Lazaro, R. N., Gadsden, H, Avila, L. J., Morando, M, De la Riva, I. J., Sepulveda, P. V., Rocha, C. F. D., Ibarguengoytia, N, Puntriano, C. A., Massot, M, Lepetz, V, Oksanen, T. A., Chapple, D. G., Bauer, A. M., Branch, W. R., Clobert, J, and Sites, J. W. (2010). Erosion of lizard diversity by climate change and altered thermal niches. Science 328, 894–899.
Erosion of lizard diversity by climate change and altered thermal niches.Crossref | GoogleScholarGoogle Scholar | 20466932PubMed |

Stevenson, R. D. (1985). The relative importance of behavioral and physiological adjustments controlling body temperature in terrestrial ectotherms. American Naturalist 126, 362–386.
The relative importance of behavioral and physiological adjustments controlling body temperature in terrestrial ectotherms.Crossref | GoogleScholarGoogle Scholar |

Sunday, J. M., Bates, A. E., Kearney, M. R., Colwell, R. K., Dulvy, N. K., Longino, J. T., and Huey, R. N. (2014). Thermal-safety margins and necessity of thermoregulatory behaviour across latitude and elevation. Proceedings of the National Academy of Sciences of the United States of America 111, 5610–5615.
Thermal-safety margins and necessity of thermoregulatory behaviour across latitude and elevation.Crossref | GoogleScholarGoogle Scholar | 24616528PubMed |

Thuiller, W. (2007). Climate change and the ecologist. Nature 448, 550–552.
Climate change and the ecologist.Crossref | GoogleScholarGoogle Scholar | 17671497PubMed |

Uller, T., Pen, I., Wapstra, E., Beukeboom, L. W., and Komdeur, J. (2007). The evolution of sex ratios and sex-determining systems. Trends in Ecology & Evolution 22, 292–297.
The evolution of sex ratios and sex-determining systems.Crossref | GoogleScholarGoogle Scholar |

Uller, T, While, G. M., Cadby, C. D., Harts, A, O’Connor, K, Pen, I, and Wapstra, E (2011). Thermal opportunity, maternal effects, and offspring survival at different climatic extremes in a viviparous lizard. Evolution 65, 2313–2324.
| 21790577PubMed |

Valdecantos, S., Martinez, V., Lobo, F., and Cruz, F. B. (2013). Thermal biology of Liolaemus lizards from the high Andes: being efficient despite adversity. Journal of Thermal Biology 38, 126–134.
Thermal biology of Liolaemus lizards from the high Andes: being efficient despite adversity.Crossref | GoogleScholarGoogle Scholar |

van Berkum, F. H. (1986). Evolutionary patterns of the thermal sensitivity of sprint speed in Anolis lizards. Evolution 40, 594–604.
Evolutionary patterns of the thermal sensitivity of sprint speed in Anolis lizards.Crossref | GoogleScholarGoogle Scholar | 28556314PubMed |

Van Damme, R., Bauwens, D., Castilla, A. M., and Verheyen, R. F. (1989). Altitudinal variation of the thermal biology and running performance in the lizard Podarcis tiliguerta. Oecologia 80, 516–524.
Altitudinal variation of the thermal biology and running performance in the lizard Podarcis tiliguerta.Crossref | GoogleScholarGoogle Scholar | 28312838PubMed |

Vidal, M. A., Habit, A., Victoriano, P., Gonzalez-Gajardo, A., and Ortiz, J. C. (2010). Thermoregulation and activity pattern of the high-mountain lizard Phymaturus palluma (Tropiduridae) in Chile. Zoologia 27, 13–18.
Thermoregulation and activity pattern of the high-mountain lizard Phymaturus palluma (Tropiduridae) in Chile.Crossref | GoogleScholarGoogle Scholar |

Wapstra, E. (2000). Maternal basking opportunities affects juvenile phenotype in a viviparous lizard. Functional Ecology 14, 345–352.
Maternal basking opportunities affects juvenile phenotype in a viviparous lizard.Crossref | GoogleScholarGoogle Scholar |

Wapstra, E., and Swain, R. (1996). Feeding ecology of the Tasmanian spotted skink, Niveoscincus ocellatus (Squamata: Scincidae). Australian Journal of Zoology 44, 205–213.
Feeding ecology of the Tasmanian spotted skink, Niveoscincus ocellatus (Squamata: Scincidae).Crossref | GoogleScholarGoogle Scholar |

Wapstra, E., and Swain, R. (2001). Geographic and annual variation in life history traits in a small Australian skink. Journal of Herpetology 35, 194–203.
Geographic and annual variation in life history traits in a small Australian skink.Crossref | GoogleScholarGoogle Scholar |

Wapstra, E., Swain, R., Jones, S. M., and O’Reilly, J. (1999). Geographic and annual variation in reproductive cycles in the Tasmanian spotted snow skink, Niveoscincus ocellatus (Squamata: Scincidae). Australian Journal of Zoology 47, 539–550.
Geographic and annual variation in reproductive cycles in the Tasmanian spotted snow skink, Niveoscincus ocellatus (Squamata: Scincidae).Crossref | GoogleScholarGoogle Scholar |

Wapstra, E., Swain, R., and O’Reilly, J. M. (2001). Geographic variation in age and size at maturity in a small Australian viviparous skink. Copeia 2001, 646–655.
Geographic variation in age and size at maturity in a small Australian viviparous skink.Crossref | GoogleScholarGoogle Scholar |

Wapstra, E., Uller, T., Sinn, D. L., Olsson, M., Mazurek, K., Joss, J., and Shine, R. (2009). Climate effects on offspring sex ratio in a viviparous lizard. Journal of Animal Ecology 78, 84–90.
Climate effects on offspring sex ratio in a viviparous lizard.Crossref | GoogleScholarGoogle Scholar | 18811661PubMed |

Wapstra, E., Uller, T., While, G., Olsson, M., and Shine, R. (2010). Giving offspring a head start in life: field and experimental evidence for selection on maternal basking behaviour in lizards. Journal of Evolutionary Biology 23, 651–657.
Giving offspring a head start in life: field and experimental evidence for selection on maternal basking behaviour in lizards.Crossref | GoogleScholarGoogle Scholar | 20074306PubMed |

Williams, S. E., Bolitho, E. E., and Fox, S. (2003). Climate change in Australian tropical rainforest: an impending environmental catastrophe. Proceedings of the Royal Society of London Series B: Biological Sciences 270, 1887–1892.
Climate change in Australian tropical rainforest: an impending environmental catastrophe.Crossref | GoogleScholarGoogle Scholar | 14561301PubMed |

Wilson, R. S. (2001). Geographic variation in the thermal sensitivity of jumping performance in the frog Limnodynastes peronei. The Journal of Experimental Biology 204, 4227–4236.
| 11815647PubMed |

Yuni, L. P. E. K. (2016). Thermal biology of the spotted snow skink, Niveoscincus ocellatus, in a warming world. Ph.D. Thesis, University of Tasmania, Hobart.

Yuni, L. P. E. K., Jones, S. M., and Wapstra, E. (2015). Energy expenditure of the spotted snow skink, Niveoscincus ocellatus, at two climatic extremes of its distribution ranges. Journal of Thermal Biology 52, 208–216.
Energy expenditure of the spotted snow skink, Niveoscincus ocellatus, at two climatic extremes of its distribution ranges.Crossref | GoogleScholarGoogle Scholar |

Zamora-Camacho, F. J., Reguera, S., Moreno-Rueda, G., and Pleguezuelos, J. M. (2013). Patterns of seasonal activity in a Mediterranean lizard along a 2200 m altitudinal gradient. Journal of Thermal Biology 38, 64–69.
Patterns of seasonal activity in a Mediterranean lizard along a 2200 m altitudinal gradient.Crossref | GoogleScholarGoogle Scholar |