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

Biogeographical effects on body mass of native Australian and introduced mice, Pseudomys hermannsburgensis and Mus domesticus: an inquiry into Bergmann’s Rule

Sean Tomlinson A B and Philip C. Withers A
+ Author Affiliations
- Author Affiliations

A School of Animal Biology, The University of Western Australia, Perth, WA 6009, Australia.

B Corresponding author. Email: tomlis01@student.uwa.edu.au

Australian Journal of Zoology 56(6) 423-430 https://doi.org/10.1071/ZO08086
Submitted: 12 November 2008  Accepted: 19 February 2009   Published: 18 March 2009

Abstract

We investigated interactions of body mass with geographical location, and five climatic measures for two Australian rodents, the native Australian sandy inland mouse (Pseudomys hermannsburgensis) and the introduced house mouse (Mus domesticus). Correlation and regression analyses identified interactions of body mass with latitude, longitude, average highest maximum and lowest minimum temperatures, average annual rainfall, rainfall variability, and aridity. There was a significant correlation of body mass with latitude and longitude for Mus domesticus and P. hermannsburgensis. House mice were heavier in the south and east, and sandy inland mice were heavier in the north and east. M. domesticus conforms to Bergmann’s Rule, while P. hermannsburgensis does not. Maximum temperature, aridity and rainfall variability significantly influenced body mass of M. domesticus, which was heavier at cooler maxima, in less arid areas, and in areas of greater rainfall variability. Only aridity significantly influenced body mass of P. hermannsburgensis, which was heavier in more arid areas. Temperature did not interact significantly with body mass. After accounting for climatic variables, there was still a significant relationship between the residuals of body mass with locality for both species, with a negative influence of latitude and a positive influence of longitude in both; the latitudinal interaction for both species was converse to Bergmann’s Rule. We suggest that latitude, ambient temperature and other selection pressures (such as aridity or productivity) can act in opposing directions, and speculate that the influence of other factors, such as food availability or sociality, may be more important than latitude or ambient temperature.


Acknowledgements

We thank the Pest Animal Control CRC and the UWA School of Animal Biology for the funding support that made this project possible, and Jamie O’Shea, Brenton Knott and Shane Maloney for their invaluable advice. We further acknowledge the contributions of numerous people and institutions across Australia in donating morphometric measurements and capture locations. Specifically, these are Ric How (Western Australian Museum) for his help with data, and his additional help with contacts nation-wide, Steve van Dyck and Heather Janetzki (Queensland Museum), Chris Dickman and Mathew Crowther (Sydney University), Jeff Cole (DIPE Northern Territory), Jeff Foulkes (Department of Environment and Heritage, South Australia) and David Stemmer (South Australia Museum), Steve Morton and Julian Reid (CSIRO), Graham Thompson (Edith Cowan University), Mark Cowan (DEC Western Australia), Jason Fraser (UWA), and David Pearson (DEC Western Australia).


References

Adams, D. C. , and Church, J. O. (2008). Amphibians do not follow Bergmann’s Rule. Evolution 62, 413–420.
Crossref | GoogleScholarGoogle Scholar | PubMed | Breed W. G. (1983). The sandy inland mouse. In ‘The Australian Museum Complete Book of Australian Mammals’. (Ed. R. Strahan.) 407 pp. (Angus and Robertson: Sydney.)

Bureau of Meteorology(2007). http://www.bom.gov.au Bureau of Meteorology, Australia.

Burnham K. P. , and Anderson D. R. (1998). ‘Model Selection and Multimodel Inference: A Practical Information-Theoretic Approach.’ (Springer: New York.)

De Queiroz, A. , and Ashton, K. G. (2004). The phylogeny of a species-level tendency: species heritability and possible deep origins of Bergmann’s Rule in tetrapods. Evolution 58, 1674–1684.
Crossref | GoogleScholarGoogle Scholar | PubMed | Gentillli J. (1971). The main climatological elements. In ‘Climates of Australia and New Zealand’. (Ed. J. Gentilli.) pp. 119–188. (Elsevier: Amsterdam.)

Gosline, A. (2004). Finding out why big is warm but small is cool. New Scientist 11(Sept), 9.
Lee A. K. , Baverstock P. R. , and Watts C. H. S. (1981). Rodents – the late invaders. In ‘Ecological Biogeography of Australia’. (Ed. A. Keast.) pp. 1523–1552. (Junk: The Hague.)

Lindstedt, S. L. , and Boyce, M. S. (1985). Seasonality, fasting endurance, and body size in mammals. American Naturalist 125, 873–878.
Crossref | GoogleScholarGoogle Scholar | Mayr E. (1963). ‘Animal Species and Evolution.’ (Harvard University Press: Cambridge, MA.)

McNab, B. K. (1970). Body weight and the energetics of temperature regulation. Journal of Experimental Biology 53, 329–348.
CAS | PubMed | McNab B. K. (2002). ‘The Physiological Ecology of Vertebrates.’ A View from Energetics.’ (Cornell University Press: Ithaca.)

Meiri, S. , and Dayan, T. (2003). On the validity of Bergmann’s Rule. Journal of Biogeography 30, 331–351.
Newsome A. E. (1983). The house mouse. In ‘The Australian Museum Complete Book of Australian Mammals’. (Ed. R. Strahan.) p. 455. (Angus and Robertson Publishers: Sydney.)

Ochocińska, D. , and Taylor, J. R. E. (2003). Bergmann’s rule in shrews: geographical variation of body size in Palearctic Sorex species. Biological Journal of the Linnean Society 78, 365–381.
Crossref | GoogleScholarGoogle Scholar | Ricklefs R. E. (1973). ‘Ecology.’ (Chiron Press: Newton, MA.)

Scantlebury, M. , Bennett, N. C. , Speakman, J. R. , Pillay, N. , and Schradin, C. (2006). Huddling in groups leads to daily energy savings in free-living African four-striped grass mice, Rhabdomys pumilio. Functional Ecology 20, 166–173.
Crossref | GoogleScholarGoogle Scholar | Schmidly D. J. , Wilkins K. T., and Derr J. N. (1993). Biogeography. In ‘Biology of the Heteromyidae’. (Eds H. H. Genoways and J. H. Brown.) pp. 319–356. (American Society of Mammalogists.)

Singleton, G. R. , Brown, P. R. , Pech, R. P. , Jacob, J. , Mutze, G. J. , and Krebs, C. J. (2005). One hundred years of eruptions of house mice in Australia – a natural biological curio. Biological Journal of the Linnean Society 84, 617–627.
Crossref | GoogleScholarGoogle Scholar | Withers P. C. (1992). ‘Comparative Animal Physiology.’ (Saunders College Publishing: Fort Worth.)

Withers, P. C. , and Jarvis, J. U. M. (1980). The effect of huddling on thermoregulation and oxygen consumption for the naked mole-rat. Comparative Biochemistry and Physiology. A. Comparative Physiology 66, 215–219.
Crossref | GoogleScholarGoogle Scholar |

Withers, P. C. , Cooper, C. E. , and Larcombe, A. N. (2006). Environmental correlates of physiological variables in marsupials. Physiological and Biochemical Zoology 79, 437–453.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

Yahav, S. , and Buffenstein, R. (1991). Huddling behavior facilitates homeothermy in the naked mole-rat Heterocephalus glaber. Physiological Zoology 64, 871–884.


Yom-Tov, Y. , Benjamini, Y. , and Kark, S. (2002). Global warming, Bergmann’s rule and body mass: are they related? The chukar partridge (Alectoris chukar) case. Journal of Zoology 257, 449–455.
Crossref | GoogleScholarGoogle Scholar |