Free Standard AU & NZ Shipping For All Book Orders Over $80!
Register      Login
Wildlife Research Wildlife Research Society
Ecology, management and conservation in natural and modified habitats
RESEARCH ARTICLE

Space use by female agile antechinus: are teat number and home-range size linked?

Juliey Beckman A and Alan Lill B C
+ Author Affiliations
- Author Affiliations

A College of Medicine, Biology and Environment, Australian National University, Canberra, ACT 2601, Australia.

B Department of Ecology, Environment and Evolution, School of Life Sciences, La Trobe University, Bundoora, Vic. 3086, Australia.

C Corresponding author. Email: A.Lill@latrobe.edu.au

Wildlife Research 43(4) 348-357 https://doi.org/10.1071/WR16001
Submitted: 4 January 2016  Accepted: 11 May 2016   Published: 6 July 2016

Abstract

Context: The number of teats that a female agile antechinus (Antechinus agilis) possesses effectively determines her initial litter size. In the Otway Ranges, south-eastern Australia, numerous separate populations in which all females have either six or 10 teats occur fairly close together in similar, contiguous forest at comparable altitudes and latitudes. Six-teat and 10-teat females have a similar mean mass, but the latter have a 1.7 × greater reproductive potential and so should have a greater nutritional requirement while raising young than do six-teat females. Theoretically, they could meet this requirement by occupying larger and/or more exclusive home ranges during breeding than do six-teat females do (provided that their food-resource abundance is comparable), albeit at a greater energetic cost.

Aims: The aim of the study was to determine whether 10-teat A. agilis females occupied larger and less overlapping home ranges than did six-teat females. To interpret the findings more meaningfully, it was necessary to compare food abundance and habitat characteristics in areas occupied by the two phenotypes.

Methods: The investigation was conducted in six-teat and 10-teat A. agilis areas in cool temperate forest over 22 months. Population density was determined by mark–recapture methods and arthropod prey biomass and abundance by pitfall trapping. Vegetation structure and plant-taxa abundance and diversity were determined by standard plant-survey methods. Female home-range estimates determined by radio-tracking were based on 95% minimal convex polygons (MCP) and kernel analysis. Home-range overlap was based on 80% MCP range determinations and core areas were calculated from utilisation plots.

Key results: Female population density was 2.5 × lower in exclusively 10-teat than in exclusively six-teat populations. Radio-tracked 10-teat females’ home ranges less commonly overlapped those of identified female neighbours and, on average, were 1.5 × larger than ranges of six-teat females. Food abundance and composition was similar in six-teat and 10-teat areas, but ground cover was denser and more complex in the latter areas.

Conclusions: Food-resource availability was similar in the six-teat and 10-teat phenotype areas, so the larger, and probably more exclusive, home ranges of 10-teat females could reflect greater nutritional requirements resulting from having larger litters, and account for their lower population density.

Implications: The A. agilis teat-number variation pattern in the Otways may be a rare, visible example of ongoing incipient speciation. This makes it of great scientific and conservation value and it is important to document how the phenomenon operates.

Additional keywords: food abundance, habitat composition, nest sites, radio-tracking.


References

Abdi, H. (2007). The Bonferroni and Sidák corrections for multiple comparisons. In ‘Encyclopedia of Measurement and Statistics.’ (Ed. N. J. Salkind.) pp. 1–9. (Sage Publications Inc.: Thousand Oaks, CA.)

Avise, J. C. (2004). ‘Phylogeography: the History and Formation of Species.’ (Harvard University Press: Cambridge, MA.)

Beckman, J. (2009). Genetic, morphological and ecological variation among populations of agile antechinus that differ in female teat-number. Ph.D. Thesis, Monash University, Melbourne.

Beckman, J., and Lill, A. (2008). Is morphometric variation associated with teat-number differences in Antechinus agilis and A. swainsonii? Observations from the Otway Ranges, Victoria. Australian Mammalogy 29, 177–190.

Beckman, J., Banks, S. C., Sunnucks, P., Lill, A., and Taylor, A. C. (2007). Phylogeography and environmental correlates of a cap on reproduction: teat number in a small marsupial, Antechinus agilis. Molecular Ecology 16, 1069–1083.
Phylogeography and environmental correlates of a cap on reproduction: teat number in a small marsupial, Antechinus agilis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXksVykt7o%3D&md5=f1b2f8b25a1c4d68bb6dcc0dd42d9573CAS | 17305861PubMed |

Both, C., and Visser, M. E. (2003). Density dependence, territoriality, and divisibility of resources: from optimality models to population processes. American Naturalist 161, 326–336.
Density dependence, territoriality, and divisibility of resources: from optimality models to population processes.Crossref | GoogleScholarGoogle Scholar | 12675376PubMed |

Braithwaite, R. W., and Lee, A. K. (1979). A mammalian example of semelparity. American Naturalist 113, 151–155.
A mammalian example of semelparity.Crossref | GoogleScholarGoogle Scholar |

Bramwell, T. (2006). Reproductive isolation between adjacent antechinus populations with different teat numbers. B.Sc.(Hons) Thesis, Monash University, Melbourne.

Burt, W. H. (1943). Territoriality and home range concepts as applied to mammals. Journal of Mammalogy 24, 346–352.
Territoriality and home range concepts as applied to mammals.Crossref | GoogleScholarGoogle Scholar |

Chojnacky, D. C., and Milton, M. (2008). Measuring carbon in shrubs. In ‘Field Measurements of Forest Carbon Monitoring: a Landscape-scale Approach’. (Ed. C. M. Hoover.) pp. 45–72. (Springer Science + Business Media BV., Netherlands)

Clarke, K. R., and Warwick, R. M. (2001). ‘Change in Marine Communities: an Approach to Statistical Analysis and Interpretation.’ 2nd edn. (PRIMER-E., Plymouth, UK.)

Cockburn, A. (1992). The duration of lactation in Antechinus stuartii Marsupialia Dasyuridae. Australian Journal of Zoology Supplementary Series 40, 195–204.
The duration of lactation in Antechinus stuartii Marsupialia Dasyuridae.Crossref | GoogleScholarGoogle Scholar |

Cockburn, A., and Lazenby-Cohen, K. A. (1992). Use of nest trees by Antechinus stuartii, a semelparous lekking marsupial. Journal of Zoology 226, 657–680.
Use of nest trees by Antechinus stuartii, a semelparous lekking marsupial.Crossref | GoogleScholarGoogle Scholar |

Cockburn, A., Lee, A. K., and Martin, R. W. (1983). Macrogeographic variation in litter size in antechinus (Marsupialia: Dasyuridae). Evolution 37, 86–95.
Macrogeographic variation in litter size in antechinus (Marsupialia: Dasyuridae).Crossref | GoogleScholarGoogle Scholar |

Dickman, C. R. (1986). An experimental manipulation of the intensity of interspecific competition: effects on a small marsupial. Oecologia 70, 536–543.
An experimental manipulation of the intensity of interspecific competition: effects on a small marsupial.Crossref | GoogleScholarGoogle Scholar |

Dickman, C. R. (1989). Demographic responses of Antechinus stuartii (Marsupialia) to supplementary food. Australian Journal of Ecology 14, 387–398.
Demographic responses of Antechinus stuartii (Marsupialia) to supplementary food.Crossref | GoogleScholarGoogle Scholar |

Dickman, C. R. (1991). Use of trees by ground-dwelling mammals: implications for management. In ‘Conservation of Australia’s Forest Fauna’. (Ed. D. Lunney.) pp. 125–136. (Royal Zoological Society of New South Wales: Sydney.)

Dickman, C. R., Parnaby, H. E., Crowther, M. S., and King, D. H. (1998). Antechinus agilis (Marsupialia: Dasyuridae), a new species from the A. stuartii complex in south-eastern Australia. Australian Journal of Zoology 46, 1–26.
Antechinus agilis (Marsupialia: Dasyuridae), a new species from the A. stuartii complex in south-eastern Australia.Crossref | GoogleScholarGoogle Scholar |

Efford, M. G., Warburton, B., Coleman, M. C., and Barker, R. J. (2005). A field test of two methods for density estimation. Wildlife Society Bulletin 33, 731–738.
A field test of two methods for density estimation.Crossref | GoogleScholarGoogle Scholar |

Goldingay, R. L. (2015). A review of home-range studies on Australian terrestrial vertebrates: adequacy of studies, testing of hypotheses, and relevance to conservation and international studies. Australian Journal of Zoology 63, 136–146.
A review of home-range studies on Australian terrestrial vertebrates: adequacy of studies, testing of hypotheses, and relevance to conservation and international studies.Crossref | GoogleScholarGoogle Scholar |

Green, K. (1989). Altitudinal and seasonal differences in the diets of Antechinus swainsonii and Antechinus stuartii (Marsupialia: Dasyuridae) in the Snowy Mountains, New South Wales, Australia. Australian Wildlife Research 16, 509–516.
Altitudinal and seasonal differences in the diets of Antechinus swainsonii and Antechinus stuartii (Marsupialia: Dasyuridae) in the Snowy Mountains, New South Wales, Australia.Crossref | GoogleScholarGoogle Scholar |

Harris, S., Creswell, W. J., Forde, P. G., Trewella, W. J., Woollard, T., and Wray, S. (1990). Home-range analysis using radio-tracking data: a review of problems and techniques particularly as applied to mammals. Mammal Review 20, 97–123.
Home-range analysis using radio-tracking data: a review of problems and techniques particularly as applied to mammals.Crossref | GoogleScholarGoogle Scholar |

James, P. L., and Heck, K. L. (1994). The effects of habitat complexity and light intensity on ambush predation within a simulated seagrass habitat. Journal of Experimental Marine Biology and Ecology 176, 187–200.
The effects of habitat complexity and light intensity on ambush predation within a simulated seagrass habitat.Crossref | GoogleScholarGoogle Scholar |

Jordan, M. A., Snell, H. L., Snell, H. M., and Jordan, W. C. (2005). Phenotypic divergence despite high levels of gene flow in Galapagos lava lizards (Microlophus albemarlensis). Molecular Ecology 14, 859–867.
Phenotypic divergence despite high levels of gene flow in Galapagos lava lizards (Microlophus albemarlensis).Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXjtVGit7k%3D&md5=b0cb2cd3388462dd5e4d1ad4931b2823CAS | 15723677PubMed |

Kenward, R. E. (2000). ‘A Manual for Wildlife Radio Tagging.’ (AP Professional: Boston, MA.)

Kenward, R. E., and Hodder, K. H. (1996). ‘Ranges V. An Analysis System for Biological Location Data.’ (Institute for Terrestrial Ecology: Dorset, UK.)

Lazenby-Cohen, K. A., and Cockburn, A. (1991). Social and foraging components of the home range in Antechinus stuartii (Dasyuridae: Marsupialia). Australian Journal of Ecology 16, 301–307.
Social and foraging components of the home range in Antechinus stuartii (Dasyuridae: Marsupialia).Crossref | GoogleScholarGoogle Scholar |

Lee, A. K., and Cockburn, A. (1985). ‘Evolutionary Ecology of Marsupials.’ (Cambridge University Press: Melbourne.)

Lunney, D., Matthews, A., and Grigg, G. (2001). The diet of Antechinus agilis and A. swainsonii in unlogged and regenerating sites in Mumbulla State Forest, south-eastern New South Wales. Wildlife Research 28, 459–464.
The diet of Antechinus agilis and A. swainsonii in unlogged and regenerating sites in Mumbulla State Forest, south-eastern New South Wales.Crossref | GoogleScholarGoogle Scholar |

Martin, J. K., and Martin, A. A. (2007). Resource distribution influences mating system in the bobuck (Trichosurus cunninghami: Marsupialia). Oecologia 154, 227–236.
Resource distribution influences mating system in the bobuck (Trichosurus cunninghami: Marsupialia).Crossref | GoogleScholarGoogle Scholar | 17713792PubMed |

Mitchell, M. S., and Powell, R. A. (2007). Optimal use of resources structures: home ranges and spatial distribution of black bears. Animal Behaviour 74, 219–230.
Optimal use of resources structures: home ranges and spatial distribution of black bears.Crossref | GoogleScholarGoogle Scholar |

Moorcroft, P. R., and Lewis, M. A. (2013). ‘Mechanistic Home Range Analysis.’ (Princeton University Press: Princeton, NJ.)

Moro, D. (1991). The distribution of small mammal species in relation to heath vegetation near Cape Otway, Victoria. Wildlife Research 18, 605–618.
The distribution of small mammal species in relation to heath vegetation near Cape Otway, Victoria.Crossref | GoogleScholarGoogle Scholar |

Nams, V. O. (2006). ‘Locate II User’s Guide.’ (Pacer, Nova Scotia, Canada.)

Otis, D. L., and White, G. C. (1999). Autocorrelation of location estimates and the analysis of radio-tracking data. The Journal of Wildlife Management 63, 1039–1044.
Autocorrelation of location estimates and the analysis of radio-tracking data.Crossref | GoogleScholarGoogle Scholar |

Powell, R. A. (2000). Animal home ranges and territories and home range estimators. In ‘Research Techniques in Animal Ecology. Controversies and Consequences’. (Eds L. Boitani and T. K. Fuller.) pp. 65–110. (Columbia University Press: New York.)

Powell, R. A., Zimmerman, J. W., and Seaman, D. E. (1997). ‘Ecology and Behavior of North American Black Bears; Home Ranges, Habitat and Social Organization.’ (Chapman and Hall: London.)

Rhind, S. G., Bradley, J. S., and Cooper, N. K. (2001). Morphometric variation and taxonomic status of brush-tailed phascogales, Phascogale tapoatafa (Meyer, 1793) (Marsupialia: Dasyuridae). Australian Journal of Zoology 49, 345–368.
Morphometric variation and taxonomic status of brush-tailed phascogales, Phascogale tapoatafa (Meyer, 1793) (Marsupialia: Dasyuridae).Crossref | GoogleScholarGoogle Scholar |

Seaman, D. E., and Powell, R. A. (1996). An evaluation of the accuracy of kernel density estimators for home range analysis. Ecology 77, 2075–2085.
An evaluation of the accuracy of kernel density estimators for home range analysis.Crossref | GoogleScholarGoogle Scholar |

Selwood, L. (1983). Factors influencing pre-natal fertility in the brown marsupial mouse, Antechinus stuartii. Journal of Reproduction and Fertility 68, 317–324.
Factors influencing pre-natal fertility in the brown marsupial mouse, Antechinus stuartii.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaL3s3ktFCmtQ%3D%3D&md5=30313e6a58454e0badedb6b33c62bc9fCAS | 6864648PubMed |

Sharpe, D. J., and Goldingay, R. L. (2007). Home range of the Australian squirrel glider, Petaurus norfolcensis (Diprotodontia). Journal of Mammalogy 88, 1515–1522.
Home range of the Australian squirrel glider, Petaurus norfolcensis (Diprotodontia).Crossref | GoogleScholarGoogle Scholar |

Shimmin, G. A., Taggart, D. A., and Temple-Smith, P. D. (2000). Variation in reproductive surpluses of the agile antechinus (Antechinus agilis) at different teat-number locations. Australian Journal of Zoology 48, 511–517.
Variation in reproductive surpluses of the agile antechinus (Antechinus agilis) at different teat-number locations.Crossref | GoogleScholarGoogle Scholar |

South, A. (1999). Extrapolating from individual movement behaviour to population spacing patterns in a ranging mammal. Ecological Modelling 117, 343–360.
Extrapolating from individual movement behaviour to population spacing patterns in a ranging mammal.Crossref | GoogleScholarGoogle Scholar |

Sutherland, D., and Predavec, M. (1999). The effects of moonlight on microhabitat use by Antechinus agilis (Marsupialia: Dasyuridae). Australian Journal of Zoology 47, 1–17.
The effects of moonlight on microhabitat use by Antechinus agilis (Marsupialia: Dasyuridae).Crossref | GoogleScholarGoogle Scholar |

Yeatman, G. J., and Wayne, A. F. (2015). Seasonal home range and habitat use of a critically endangered marsupial (Bettongia penicillata ogilbyi) inside and outside a predator-proof sanctuary. Australian Mammalogy 37, 157–163.
Seasonal home range and habitat use of a critically endangered marsupial (Bettongia penicillata ogilbyi) inside and outside a predator-proof sanctuary.Crossref | GoogleScholarGoogle Scholar |

Yuncken, D. (1997). Diet and prey availability of Antechinus stuartii (Marsupialia: Dasyuridae). B.Sc.(Hons) Thesis, Monash University, Melbourne.