nature.com

Female mating bias results in conflicting sex-specific offspring fitness - Nature

  • ️Mousseau, Timothy A.
  • ️Thu May 06 2004
  • Letter
  • Published: 06 May 2004

Nature volume 429pages 65–67 (2004)Cite this article

Abstract

Indirect-benefit models of sexual selection assert that females gain heritable offspring advantages through a mating bias for males of superior genetic quality. This has generally been tested by associating a simple morphological quality indicator (for example, bird tail length) with offspring viability1. However, selection acts simultaneously on many characters, limiting the ability to detect significant associations, especially if the simple indicator is weakly correlated to male fitness2,3. Furthermore, recent conceptual developments suggest that the benefits gained from such mating biases may be sex-specific because of sexually antagonistic genes that differentially influence male and female reproductive ability4. A more suitable test of the indirect-benefit model would examine associations between an aggregate quality indicator1,3 (such as male mating success) and gender-specific adult fitness components, under the expectation that these components may trade off1. Here, we show that a father's mating success in the cricket, Allonemobius socius, is positively genetically correlated with his son's mating success but negatively with his daughter's reproductive success. This provides empirical evidence that a female mating bias can result in sexually antagonistic offspring fitness.

This is a preview of subscription content, access via your institution

Access options

Subscribe to this journal

Receive 51 print issues and online access

$199.00 per year

only $3.90 per issue

Buy this article

  • Purchase on SpringerLink
  • Instant access to full article PDF

Prices may be subject to local taxes which are calculated during checkout

Additional access options:

Figure 1: Female mating bias resulted in conflicting sex-specific offspring fitness.

Similar content being viewed by others

References

  1. Kokko, H. Fisherian and ‘good genes’ benefits of mate choice: how (not) to distinguish between them. Ecol. Lett. 4, 322–326 (2001)

    Article  Google Scholar 

  2. Boake, C. R. B. Genetic consequences of mate choice: a quantitative genetic method for testing sexual selection theory. Science 227, 1061–1063 (1985)

    Article  ADS  CAS  Google Scholar 

  3. Heisler, I. L. Quantitative genetic models of female choice based on “arbitrary” male characters. Heredity 55, 187–198 (1985)

    Article  Google Scholar 

  4. Chippindale, A. K., Gibson, J. R. & Rice, W. R. Negative genetic correlation for adult fitness between sexes reveals ontogenetic conflict in Drosophila. Proc. Natl Acad. Sci. USA 98, 1671–1675 (2001)

    Article  ADS  CAS  Google Scholar 

  5. Rice, W. R. Dangerous liaisons. Proc. Natl Acad. Sci. USA 97, 12953–12955 (2000)

    Article  ADS  CAS  Google Scholar 

  6. Chapman, T., Arnqvist, G., Bangham, J. & Rowe, L. Sexual conflict. Trends Ecol. Evol. 18, 41–47 (2003)

    Article  Google Scholar 

  7. Fedorka, K. M. & Mousseau, T. A. Tibial spur feeding in ground crickets: larger males contribute larger gifts (Orthoptera: Gryllidae). Florida Entomol. 85, 317–323 (2002)

    Article  Google Scholar 

  8. Fedorka, K. M. & Mousseau, T. A. Nuptial gifts and the evolution of male body size. Evolution 56, 590–596 (2002)

    Article  Google Scholar 

  9. Wedell, N. & Tregenza, T. Successful fathers sire successful sons. Evolution 53, 620–625 (1999)

    Article  CAS  Google Scholar 

  10. Mousseau, T. A. & Dingle, H. Maternal effects in insect life histories. Annu. Rev. Entomol. 36, 511–534 (1991)

    Article  Google Scholar 

  11. Mousseau, T. A. & Dingle, H. in The Unity of Evolutionary Biology (ed. Dudley, E. C.) 745–761 (Dioscorides, Portland, Oregon, 1991)

    Google Scholar 

  12. Roff, D. A. Evolutionary Quantitative Genetics (Chapman & Hall, New York, 1997)

    Book  Google Scholar 

  13. Montalvo, A. M. & Shaw, R. G. Quantitative genetics of sequential life history and juvenile traits in the partially selfing perennial, Aquilegia caerulea. Evolution 48, 828–841 (1994)

    Article  Google Scholar 

  14. Zar, J. H. Biostatistical Analysis 2nd edn, 324 (Prentice Hall, Englewood Cliffs, New Jersey, 1984)

    Google Scholar 

  15. Lynch, M. & Walsh, B. Genetics and Analysis of Quantitative Traits 632–637 (Sinauer Associates, Sunderland, 1998)

    Google Scholar 

Download references

Acknowledgements

We thank D. Promislow, P. Mack and J. Burger for comments on previous manuscript versions. We also thank N. Leung and A. Penn for assisting with cricket maintenance and data collection. This work was supported by a NSF Doctoral Dissertation Improvement Grant to K.M.F. and a NSF grant to T.A.M.

Author information

Author notes

  1. Kenneth M. Fedorka

    Present address: Department of Genetics, University of Georgia, Athens, Georgia, 30602, USA

Authors and Affiliations

  1. Department of Biological Sciences, University of South Carolina, Columbia, South Carolina, 29208, USA

    Kenneth M. Fedorka & Timothy A. Mousseau

Authors

  1. Kenneth M. Fedorka

    You can also search for this author in PubMed Google Scholar

  2. Timothy A. Mousseau

    You can also search for this author in PubMed Google Scholar

Corresponding author

Correspondence to Kenneth M. Fedorka.

Ethics declarations

Competing interests

The authors declare that they have no competing financial interests.

About this article

Cite this article

Fedorka, K., Mousseau, T. Female mating bias results in conflicting sex-specific offspring fitness. Nature 429, 65–67 (2004). https://doi.org/10.1038/nature02492

Download citation

  • Received: 04 February 2004

  • Accepted: 09 March 2004

  • Issue Date: 06 May 2004

  • DOI: https://doi.org/10.1038/nature02492