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Wildlife Research Wildlife Research Society
Ecology, management and conservation in natural and modified habitats
RESEARCH ARTICLE

Estimates of sex ratio require the incorporation of unequal catchability between sexes

Evan J. Pickett A B , Michelle P. Stockwell A , Carla J. Pollard A , James I. Garnham A , John Clulow A and Michael J. Mahony A
+ Author Affiliations
- Author Affiliations

A School of Environmental and Life Sciences, University of Newcastle, University Drive, Callaghan, NSW 2300, Australia.

B Corresponding author. Email: evan.pickett@uon.edu.au

Wildlife Research 39(4) 350-354 https://doi.org/10.1071/WR11193
Submitted: 24 November 2011  Accepted: 21 March 2012   Published: 26 April 2012

Abstract

Context: Estimates of the sex ratio of a population are a common summary statistic used for ecological studies and conservation planning. However, methods to determine the sex ratio often ignore capture probability, which can lead to a perceived bias in the sex ratio when the sexes are detected at different rates.

Aims: To illustrate the bias from conventional count-based analysis methods for determining sex ratio by comparison with analytical methods that include capture probability.

Methods: Closed-population mark–recapture analysis was used to determine the population size of each sex within a population of green and golden bell frogs (Litoria aurea). This was then compared with the traditional count-based methods of estimating sex ratio to determine the effect of incorporating capture probability on the sex ratio estimate.

Key results: More males than females were detected during surveys, producing a male-biased sex ratio when there was no incorporation of capture probability. Mark–recapture results indicated a similar population size between the two sexes, suggesting that the sex ratio is closer to even.

Conclusions: Methods to estimate sex ratio that incorporate capture probability can significantly reduce the bias obtained from count data.

Implications: We suggest that population studies must incorporate capture probability to determine the sex ratio of a population.

Additional keywords: Anuran, conservation, frog, Litoria aurea, mark–recapture, population ecology.


References

Alho, J. S., Herczeg, G., and Merilä, J. (2008). Female-biased sex ratios in subarctic common frogs. Journal of Zoology 275, 57–63.
Female-biased sex ratios in subarctic common frogs.Crossref | GoogleScholarGoogle Scholar |

Barbieri, F., and Bernini, F. (2004). Distribution and status of Rana latastei in Italiy (Amphibia, Ranidae). The Italian Journal of Zoology 71, 91–94.

Berven, K. A. (1990). Factors affecting population fluctuations in larval and adult stages of the wood frog (Rana sylvatica). Ecology 71, 1599–1608.
Factors affecting population fluctuations in larval and adult stages of the wood frog (Rana sylvatica).Crossref | GoogleScholarGoogle Scholar |

Bolen, W. L., and Robinson, E. G. (1995). ‘Wildlife Ecology and Management.’ (Prentice Hall: Englewood Cliffs, NJ.)

Burnham, K. P., and Anderson, D. R. (2002). ‘Model Selection and Multimodel Inference: a Practical Information-Theoretic Approach.’ (Springer-Verlag: Heidelberg, Germany.)

Christy, M. T. (1996). The efficacy of using passive integrated transponder (PIT) tags without anaesthetic in free-living frogs. Australian Zoologist 30, 139–142.

Christy, M. T. (2000). The ecology and conservation of the green and golden bell frog Litoria aurea (Lesson) (Anura: Hylidae). Ph.D. thesis, University of Sydney, Sydney.

Davis, A. K., and Rendón-Salinas, E. (2010). Are female monarch butterflies declining in eastern North America? Evidence of a 30-year change in sex ratios at Mexican overwintering sites. Biology Letters 6, 45–47.
Are female monarch butterflies declining in eastern North America? Evidence of a 30-year change in sex ratios at Mexican overwintering sites.Crossref | GoogleScholarGoogle Scholar |

Ewen, J. G., Clarke, R. H., Moysey, E., Boulton, R. L., Crozier, R. H., and Clarke, M. F. (2001). Primary sex ratio bias in an endangered cooperatively breeding bird, the black-eared miner, and its implications for conservation. Biological Conservation 101, 137–145.
Primary sex ratio bias in an endangered cooperatively breeding bird, the black-eared miner, and its implications for conservation.Crossref | GoogleScholarGoogle Scholar |

Goldingay, R. L. (2008). Conservation of the endangered green and golden bell frog: what contribution has ecological research made since 1996? Australian Zoologist 34, 335–349.

Goldingay, R. L., and Newell, D. A. (2005). Aspects of the population ecology of the green and golden bell frog Litoria aurea at the northern end of its range. Australian Zoologist 33, 49–59.

Greer, A. E., and Byrne, M. (1995). Sex ratio and frequency of the oestological abnormalities in the Australian hylid frog Litoria aurea from two apparently unpolluted localities in Sydney, New South Wales. Australian Zoologist 30, 43–47.

Haig, S. M., Belthoff, J. R., and Allen, D. H. (1993). Population viability analysis for a small population of red-cocked woodpeckers and an evaluation of enhancement strategies. Conservation Biology 7, 289–301.
Population viability analysis for a small population of red-cocked woodpeckers and an evaluation of enhancement strategies.Crossref | GoogleScholarGoogle Scholar |

Hailey, A., and Willemsen, R. E. (2000). Population density and adult sex ratio of the tortoise Testudo nermanni in Greece: evidence for intrinsic population regulation. Journal of Zoology 251, 325–338.
Population density and adult sex ratio of the tortoise Testudo nermanni in Greece: evidence for intrinsic population regulation.Crossref | GoogleScholarGoogle Scholar |

Hamer, A. J., and Mahony, M. J. (2007). Life history of an endangered amphibian challenges the declining species paradigm. Australian Journal of Zoology 55, 79–88.
Life history of an endangered amphibian challenges the declining species paradigm.Crossref | GoogleScholarGoogle Scholar |

Hamilton, W. D. (1967). Extraordinary sex ratios. Science 156, 477–488.
Extraordinary sex ratios.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaF2s7ivFOltg%3D%3D&md5=15098feb41e379ca28da66685a5e7986CAS |

Jaatinen, K., Lehikoinen, A., and Lank, D. B. (2010). Female-biased sex ratios and the proportion of cryptic male morphs of migrant juvenile ruffs (Philomachus pugnax) in Finland. Ornis Fennica 87, 1–10.

Jenouvrier, S., Caswell, H., Barbraud, C., and Weimerskirch, H. (2010). Mating behaviour, population growth, and the operational sex ratio: a periodic two-sex model approach. American Naturalist 175, 739–752.
Mating behaviour, population growth, and the operational sex ratio: a periodic two-sex model approach.Crossref | GoogleScholarGoogle Scholar |

Kéry, M., and Juillerat, L. (2004). Sex ratio estimation and survival analysis for Orthetrum coerulescens (Odonata, Libellulidae). Canadian Journal of Zoology 82, 399–406.
Sex ratio estimation and survival analysis for Orthetrum coerulescens (Odonata, Libellulidae).Crossref | GoogleScholarGoogle Scholar |

Lacy, R. C. (1993). VORTEX: a computer simulation model for population viability analysis. Wildlife Research 20, 45–65.
VORTEX: a computer simulation model for population viability analysis.Crossref | GoogleScholarGoogle Scholar |

Lemckert, F. L. (2005). Population structure, individual growth and survival of an Australian frog Crinia signifera at a pond. Acta Zoologica Sinica 51, 393–400.

Leopold, A. (1933). ‘Game Management.’ (Scribner: New York.)

Lodé, T., Holveck, M.-J., and Lesbarréres, D. (2005). Asynchronous arrival pattern, operational sex ratio and occurrence of multiple paternities in a territorial breeding anuran, Rana dalmatina. Biological Journal of the Linnean Society. Linnean Society of London 86, 191–200.
Asynchronous arrival pattern, operational sex ratio and occurrence of multiple paternities in a territorial breeding anuran, Rana dalmatina.Crossref | GoogleScholarGoogle Scholar |

Otis, D. L., Burnham, K. P., White, G. C., and Anderson, D. R. (1978). Statistical inference from capture data on closed animal populations. Wildlife Monographs 62, 1–135.

Pyke, G. H., and White, A. W. (2001). A review of the biology of the green and golden bell frog Litoria aurea. Australian Zoologist 31, 563–598.

Skalski, J. R., Ryding, K. E., and Millspaugh, J. J. (2005). Estimating population sex ratios. In ‘Wildlife Demography: analysis of Sex, Age, and Count Data’. pp. 49–87. (Elsevier: Sydney.)

Soetaert, K., and Herman, P. M. J. (2009) ‘A Practical Guide to Ecological Modelling Using R as a Simulation Platform.’ (Springer: Verlag, NY)

Solberg, E. J., Loison, A., Ringsby, T. H., Sæther, B.-E., and Heim, M. (2002). Biased adult sex ratio can affect fecundity in primiparous moose Alces alces. Wildlife Biology 8, 117–128.

Wehi, P. M., Nakagawa, S., Trewick, S. A., and Morgan-Richards, M. (2011). Does predation result in adult sex ratio skew in a sexually dimorphic insect genus? Journal of Evolutionary Biology 24, 2321–2328.
Does predation result in adult sex ratio skew in a sexually dimorphic insect genus?Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC3MbgsFemtQ%3D%3D&md5=98d296b10a249ea3b9c25a94552b0a57CAS |

White, G. C., and Burnham, K. P. (1999). Program MARK: survival estimation from populations of marked animals. Bird Study 46, S120–S139.
Program MARK: survival estimation from populations of marked animals.Crossref | GoogleScholarGoogle Scholar |