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

Ecology of Stimson’s python (Antaresia stimsoni) in the MacDonnell Ranges of central Australia

Peter J. McDonald A B D , Gary W. Luck C , Skye Wassens A and Chris R. Pavey B
+ Author Affiliations
- Author Affiliations

A School of Environmental Sciences, Charles Sturt University, PO Box 789, Albury, NSW 2640, Australia.

B Biodiversity Conservation Division, Department of Natural Resources, Environment, the Arts and Sport, PO Box 1120, Alice Springs, NT 0871, Australia.

C Institute for Land, Water and Society, Charles Sturt University, PO Box 789, Albury, NSW 2640, Australia.

D Corresponding author. Email: peterj.mcdonald@nt.gov.au

Australian Journal of Zoology 59(2) 95-102 https://doi.org/10.1071/ZO11047
Submitted: 4 July 2011  Accepted: 23 August 2011   Published: 7 October 2011

Abstract

Stimson’s python (Antaresia stimsoni) is a small nocturnal python (Pythonidae) that occurs throughout Australia’s arid zone. Despite its wide distribution and localised abundance, no field-based studies have been undertaken on this species. We investigated activity patterns, habitat use, diet, and body sizes of A. stimsoni in the MacDonnell Ranges bioregion of the Northern Territory. Data were collected at night by road-cruising along a sealed road transect over 12 consecutive months. We found that the species copes with the extreme weather variability of arid Australia by remaining active over a broad range of air temperatures and maximising activity following rainfall when relative humidity is high and ground-dwelling frogs, a significant prey source, are likely to be abundant. A. stimsoni ceased activity only during the coldest months of the year. The species occurs in a range of vegetation types, with an apparent preference for riparian woodland, and its ability to thrive in the MacDonnell Ranges may be related to the abundance of rock-outcrops for refuge. Our results for diet and body size support previous research based on museum specimens, confirming that A. stimsoni feeds on a range of terrestrial vertebrates and is not sexually dimorphic.


References

Alldredge, J. R., and Ratti, J. T. (1992). Further comparison of some statistical techniques for analysis of resource selection. Journal of Wildlife Management 56, 1–9.
Further comparison of some statistical techniques for analysis of resource selection.Crossref | GoogleScholarGoogle Scholar |

Barker, D. G., and Barker, T. M. (1994). ‘Pythons of the World: Volume 1, Australia.’ (Advanced Vivariums Systems Inc.: California.)

Bedford, G. S., and Christian, K. A. (1998). Standard metabolic rate and preferred body temperatures in some Australian pythons. Australian Journal of Zoology 46, 317–328.
Standard metabolic rate and preferred body temperatures in some Australian pythons.Crossref | GoogleScholarGoogle Scholar |

Bedford, G. S., and Christian, K. A. (2000). Digestive efficiency in some Australian pythons. Copeia 2000, 829–834.
Digestive efficiency in some Australian pythons.Crossref | GoogleScholarGoogle Scholar |

Brown, G. P., Shine, R., and Madsen, T. (2002). Responses of three sympatric snake species to tropical seasonality in northern Australia. Journal of Tropical Ecology 18, 549–568.
Responses of three sympatric snake species to tropical seasonality in northern Australia.Crossref | GoogleScholarGoogle Scholar |

Brown, W. S., and Parker, W. S. (1976). A ventral scale clipping system for permanently marking snakes (Reptilia, Serpentes). Journal of Herpetology 10, 247–249.
A ventral scale clipping system for permanently marking snakes (Reptilia, Serpentes).Crossref | GoogleScholarGoogle Scholar |

Byers, C. R., Steinhorst, R. K., and Krausman, P. R. (1984). Clarification of a technique for analysis of utilization–availability data. Journal of Wildlife Management 48, 1050–1053.
Clarification of a technique for analysis of utilization–availability data.Crossref | GoogleScholarGoogle Scholar |

Daltry, J. C., Ross, T., Thorpe, R. S., and Wuster, W. (1998). Evidence that humidity influences snake activity patterns: a field study of the Malayan pit viper Calloselasma rhodostoma. Ecography 21, 25–34.
Evidence that humidity influences snake activity patterns: a field study of the Malayan pit viper Calloselasma rhodostoma.Crossref | GoogleScholarGoogle Scholar |

Freeman, A., and Bruce, C. (2007). The things you find on the road: roadkill and incidental as an indicator of habitat use in two species of tropical pythons. In ‘Biology of the Boas and Pythons’. (Eds R. Henderson and R. Powell.) pp. 152–165. (Eagle Mountain Publishing: Eagle Mountain, UT.)

Gans, C. T., Krakaueran, D. C., and Paganelli, V. (1968). Water loss in snakes: interspecific and intraspecific variability. Comparative Biochemistry and Physiology 27, 747–761.
Water loss in snakes: interspecific and intraspecific variability.Crossref | GoogleScholarGoogle Scholar |

Geiser, F., and Pavey, C. R. (2007). Basking and torpor in a rock-dwelling desert marsupial: survival strategies in a resource-poor environment. Journal of Comparative Physiology. B, Biochemical, Systemic, and Environmental Physiology 177, 885–892.
Basking and torpor in a rock-dwelling desert marsupial: survival strategies in a resource-poor environment.Crossref | GoogleScholarGoogle Scholar |

Goodyear, S. E., and Pianka, E. R. (2008). Sympatric ecology of five species of fossorial snakes (Elapidae) in Western Australia. Journal of Herpetology 42, 279–285.
Sympatric ecology of five species of fossorial snakes (Elapidae) in Western Australia.Crossref | GoogleScholarGoogle Scholar |

Heatwole, H. (1984). Adaptation of amphibians to aridity. In ‘Arid Australia’. (Eds H. J. Cogger and E. E. Cameron.) pp. 177–222. (Australian Museum Publishing: Sydney.)

Henderson, R. W., and Hoevers, L. G. (1977). The seasonal incidence of snakes at a locality in northern Belize. Copeia 1977, 349–355.
The seasonal incidence of snakes at a locality in northern Belize.Crossref | GoogleScholarGoogle Scholar |

James, C. D., and Shine, R. (2000). Why are there so many coexisting species of lizards in Australian deserts? Oecologia 125, 127–141.
Why are there so many coexisting species of lizards in Australian deserts?Crossref | GoogleScholarGoogle Scholar |

Milne, D. J., Fisher, A., Rainey, I., and Pavey, C. R. (2005). Temporal patterns of bats in the Top End of the Northern Territory, Australia. Journal of Mammalogy 86, 909–920.
Temporal patterns of bats in the Top End of the Northern Territory, Australia.Crossref | GoogleScholarGoogle Scholar |

Nano, C. E. M., and Clarke, P. L. (2008). Variegated desert vegetation: covariation of edaphic and fire variables provides a framework for understanding mulga–spinifex coexistence. Austral Ecology 33, 848–862.
Variegated desert vegetation: covariation of edaphic and fire variables provides a framework for understanding mulga–spinifex coexistence.Crossref | GoogleScholarGoogle Scholar |

Pearson, D., Shine, R., and Williams, A. (2002). Geographic variation in sexual size dimorphism within a single snake species (Morelia spilota, Pythonidae). Oecologia 131, 418–426.
Geographic variation in sexual size dimorphism within a single snake species (Morelia spilota, Pythonidae).Crossref | GoogleScholarGoogle Scholar |

Predavec, M., and Dickman, C. R. (1993). Ecology of desert frogs: a study from southwestern Queensland. In ‘Herpetology in Australia: a diverse discipline’. (Eds D. Lunney and D. Ayers.) pp. 159–169. (Surrey Beatty: Sydney.)

Rosen, P. C., and Lowe, C. H. (1994). Highway mortality of snakes in the Sonoran Desert of southern Arizona. Biological Conservation 68, 143–148.
Highway mortality of snakes in the Sonoran Desert of southern Arizona.Crossref | GoogleScholarGoogle Scholar |

Shine, R. (1988). Food habits and reproductive biology of small Australian snakes of the genera Unechis and Suta (Elapidae). Journal of Herpetology 22, 307–315.
Food habits and reproductive biology of small Australian snakes of the genera Unechis and Suta (Elapidae).Crossref | GoogleScholarGoogle Scholar |

Shine, R. (1994). Sexual size dimorphism in snakes revisited. Copeia 1994, 326–346.
Sexual size dimorphism in snakes revisited.Crossref | GoogleScholarGoogle Scholar |

Shine, R. (1999). ‘Australian Snakes: A Natural History.’ (Reed New Holland: Sydney.)

Shine, R., and Bonnet, X. (2009). Reproductive biology, population viability, and options for field management. In ‘Snakes: Ecology and Conservation’. (Eds S. J. Mullin and R. A. Seigel.) pp. 172–200. (Cornell University Press: New York.)

Shine, R., and Slip, D. J. (1990). Biological aspects of the adaptive radiation of Australasian pythons (Serpentes: Boidae). Herpetologica 46, 283–290.

Sullivan, B. K. (2000). Long-term shifts in a snake population: a California site revisited. Biological Conservation 94, 321–325.
Long-term shifts in a snake population: a California site revisited.Crossref | GoogleScholarGoogle Scholar |

Trembath, D. F., Fearn, S., and Undheim, E. A. (2009). Natural history of the slaty grey snake (Stegonotus cucullatus) (Serpentes: Colubridae) from tropical north Queensland, Australia. Australian Journal of Zoology 57, 119–124.
Natural history of the slaty grey snake (Stegonotus cucullatus) (Serpentes: Colubridae) from tropical north Queensland, Australia.Crossref | GoogleScholarGoogle Scholar |

Webb, J. K., Christian, K. A., and Fisher, P. (2002). Fast growth and early maturation in a viviparous sit-and-wait predator, the northern death adder (Acanthophis praelongus), from tropical Australia. Journal of Herpetology 36, 505–509.

Wilson, S., and Swan, G. (2010). ‘A Complete Guide to Reptiles of Australia.’ 3rd edn. (Reed New Holland: Sydney.)