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

Thermal regimes and diel activity patterns of four species of small elapid snakes from south-eastern Australia

John Llewelyn A , Richard Shine A B and Jonathan K. Webb A
+ Author Affiliations
- Author Affiliations

A Biological Sciences A08, University of Sydney, NSW 2006, Australia.

B Corresponding author. Email: rics@bio.usyd.edu.au

Australian Journal of Zoology 53(1) 1-8 https://doi.org/10.1071/ZO04037
Submitted: 14 May 2004  Accepted: 14 January 2004   Published: 24 February 2005

Abstract

Two of the most basic biological attributes for any ectothermic animal are the times of day that it is active and the body temperatures that it exhibits. Published studies on reptile biology display a heavy bias towards diurnal lizards from Northern Hemisphere habitats. To help redress this imbalance, we quantified thermal regimes and activity times in four species of small Australian elapid snakes. Mean selected body temperature in a thermal gradient was affected by the time of testing (i.e. night v. day), with snakes choosing higher body temperatures at night than by day. In outdoor enclosures, whip snakes (Demansia psammophis) were shuttling heliotherms active only during daylight hours at relatively high body temperatures; in a laboratory thermal gradient these animals selected high body temperatures (mean 31.3°C during the day and 33.2°C at night). The other three taxa – golden-crowned snakes (Cacophis squamulosus), small-eyed snakes (Cryptophis nigrescens) and marsh snakes (Hemiaspis signata) – were active mostly at night at relatively low body temperatures, and selected low body temperatures in a thermal gradient (18.1–23.4°C). Thus, mean selected body temperatures differ substantially among sympatric elapid species in south-eastern Australia and are correlated with times of activity.


Acknowledgments

We thank M. Elphick and F. Seebacher for their encouragement and assistance, and F. Lemckert for generously providing snakes for this study. We thank two anonymous reviewers for providing critical comments and suggestions that helped to improve an earlier version of the manuscript. This work was carried out in accordance with the University of Sydney Animal Care and Ethics Committee and under a scientific licence from the NSW National Parks and Wildlife Service. The research was supported by a grant from the Australian Research Council to R. Shine and J. Webb.


References

Andren, C. (1982). Effect of prey density on reproduction, foraging and other activities in the adder, Vipera berus. Amphibia-Reptilia 3, 81–96.
Cogger H. G. (2000). ‘Reptiles and Amphibians of Australia.’ 6th edn. (Reed New Holland: Sydney.)

Cogger H., and Heatwole H. (1981). The Australian reptiles: origins, biogeography, distribution patterns and island biogeography. In ‘Ecological Biogeography of Australia’. (Ed. A. Keast.) pp. 1332–1373. (Junk: The Hague.)

Cogger H. G., Cameron E. E., and Cogger H. M. (1983). ‘Zoological Catalogue of Australia. Volume 1. Amphibia and Reptilia.’ (Australian Government Publishing Service: Canberra.)

Du, W. , Yan, S. , and Ji, X. (2000). Selected body temperature, thermal tolerance and thermal dependence of food assimilation and locomotor performance in adult blue-tailed skinks, Eumeces elegans. Journal of Thermal Biology 25, 197–202.
Crossref | GoogleScholarGoogle Scholar | Greer A. E. (1997). ‘The Biology and Evolution of Australian Snakes.’ (Surrey Beatty: Sydney.)

Hammerson, G. A. (1979). Thermal ecology of the striped racer, Masticophis lateralis. Herpetologica 35, 267–273.
Peterson C. R., Gibson A. R., and Dorcas M. E. (1993). Snake thermal ecology: the causes and consequences of body-temperature variation. In ‘Snakes: Ecology and Behavior’. (Eds R. A. Seigel and J. T. Collins.) pp. 241–314. (McGraw-Hill: New York.)

Pringle, R. M. , Webb, J. K. , and Shine, R. (2003). Canopy structure, microclimate, and habitat selection by a nocturnal snake, Hoplocephalus bungaroides. Ecology 84, 2668–2679.
Shine R. (1991). ‘Australian Snakes. A Natural History.’ (Reed Books: Sydney.)

Shine, R. , and Lambeck, R. (1990). Seasonal shifts in the thermoregulatory behaviour of Australian blacksnakes, Pseudechis porphyriacus. Journal of Thermal Biology 15, 301–305.
Crossref | GoogleScholarGoogle Scholar |

Shine, R. , Elphick, M. J. , and Barrott, E. G. (2003). Sunny side up: lethally high, not low, temperatures may prevent oviparous reptiles from reproducing at high elevations. Biological Journal of the Linnean Society 78, 325–334.
Crossref | GoogleScholarGoogle Scholar |

Webb, J. K. , and Shine, R. (1998). Thermoregulation by a nocturnal elapid snake (Hoplocephalus bungaroides) in south-eastern Australia. Physiological Zoology 71, 680–692.
PubMed |

Webb, J. K. , Pringle, R. M. , and Shine, R. (2004). How do nocturnal snakes select diurnal retreat sites? Copeia 2004, 919–925.


Whitaker, P. B. , and Shine, R. (2002). Thermal biology and activity patterns of the eastern brownsnake (Pseudonaja textilis): a radiotelemetric study. Herpetologica 58, 436–452.