Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Letter
  • Published:

Life-history traits of voles in a fluctuating population respond to the immediate environment

Abstract

Life-history traits relating to growth and reproduction vary greatly among species and populations1,2 and among individuals within populations3. In vole populations, body size and age at maturation may vary considerably among locations and among years within the same location4,5,6,7,8. Individuals in increasing populations are typically larger and start reproduction earlier in the spring than those in declining populations6,7,8. The cause of such life-history variation within populations has been subject of much discussion7,9,10. Much of the controversy concerns whether the memory of past conditions, leading to delayed effects on life-history traits, resides in the environment (for example, predators11,12, pathogens13 or food14,15) or intrinsically within populations or individuals (age distribution16,17, physiological state3, genetic18 or maternal effects19,20). Here we report from an extensive field transplant experiment in which voles were moved before the breeding season between sites that differed in average overwintering body mass. Transplanted voles did not retain the characteristics of their source population, and we demonstrate an over-riding role of the immediate environment in shaping life-history traits of small rodents.

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

Access options

Buy this article

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

Figure 1: Design of the study.
Figure 2: Average (±s.e.) individual change in body mass of transplanted voles recaptured in January/February during the first session after transplanting plotted against difference in average body mass at the sites.
Figure 3: Average body mass (±2s.e.) over the spring after the transplant.
Figure 4: Onset of spring reproduction measured as proportions of perforate and lactating females (top and middle panels) and proportion of males with scrotal testes (bottom panel).

Similar content being viewed by others

References

  1. Stearns, S. C. The Evolution of Life Histories (Oxford Univ. Press, Oxford, 1992).

    Google Scholar 

  2. Roff, D. A. The Evolution of Life Histories; Theory and Analysis (Chapman & Hall, New York, 1992).

    Google Scholar 

  3. McNamara, J. M. & Houston, A. I. State-dependent life histories. Nature 380, 215–221 (1996).

    Article  CAS  Google Scholar 

  4. Agrell, J., Erlinge, S., Nelson, J. & Sandell, M. Body weight and population dynamics: cyclic demography in a noncyclic population of the field vole (Microtus agrestis). Can. J. Zool. 70, 494–501 (1992).

    Article  Google Scholar 

  5. Taitt, M. J. & Krebs, C. J. in Biology of New World Microtus (ed. Tamarin, R. H.) 567–620 (American Soc. Mammalogists Special Publications No. 8, Shippensburg, 1985).

    Google Scholar 

  6. Chitty, D. Mortality among voles (Microtus agrestis) at Lake Vyrnwy, Montgomeryshire, in 1936–9. Phil. Trans. R. Soc. Lond. B 236, 505–552 (1952).

    Article  Google Scholar 

  7. Krebs, C. J. & Myers, J. H. Population cycles in small mammals. Adv. Ecol. Res. 8, 267–399 (1974).

    Article  Google Scholar 

  8. Tast, J. in Winter Ecology of Small Mammals (ed. Merritt, J. F.) 59–66 (Carnegie Museun of Natural History, Pittsburg, 1984).

    Google Scholar 

  9. Krebs, C. J. Population cycles revisited. J. Mamm. 77, 8–24 (1996).

    Article  Google Scholar 

  10. Stenseth, N. C. Population cycles in voles and lemmings: density dependence and phase dependence in a stochastic world. Oikos 87, 427–461 (1999).

    Article  Google Scholar 

  11. Korpimäki, E. & Krebs, C. J. Predation and population cycles of small mammals. BioScience 46, 754–764 (1996).

    Article  Google Scholar 

  12. Mappes, T., Koskela, E. & Ylönen, H. Breeding suppression in voles under predation risk of small mustelids: laboratory or methodological artifact? Oikos 82, 365–369 (1998).

    Article  Google Scholar 

  13. Soveri, T. et al. Disease patterns in field and bank vole populations during a cyclic decline in central Finland. Comp. Immunol. Microbiol. Infect. Dis. 23, 73–89 (2000).

    Article  CAS  Google Scholar 

  14. Batzli, G. O. in Wildlife 2001: Populations (eds McCullough, D. R. & Barrett, R. H.) (Elsevier Applied Sciences, London, 1992).

    Google Scholar 

  15. Agrell, J., Erlinge, S., Nelson, J., Nilsson, C. & Persson, I. Delayed density-dependence in a small-rodent population. Proc. R. Soc. Lond. B 262, 65–70 (1995).

    Article  CAS  Google Scholar 

  16. Boonstra, R. Population cycles in microtines: the senescence hypothesis. Evol. Ecol. 8, 196–219 (1994).

    Article  Google Scholar 

  17. Tkadlec, E. & Zejda, J. Small rodent population fluctuations: The effects of age structure and seasonality. Evol. Ecol. 12, 191–210 (1998).

    Article  Google Scholar 

  18. Chitty, D. The natural selection of self-regulatory behaviour in animal populations. Proc. Ecol. Soc. Aus. 2, 51–78 (1967).

    Google Scholar 

  19. Boonstra, R. & Boag, P. T. A test of the Chitty hypothesis: inheritance of life-history traits in meadow voles Microtus pennsylvanicus. Evolution 41, 929–947 (1987).

    Article  Google Scholar 

  20. Inchausti, P. & Ginzburg, L. R. Small mammal cycles in northern Europe: patterns and evidence for maternal effect hypothesis. J. Anim. Ecol. 67, 180–194 (1998).

    Article  Google Scholar 

  21. Lambin, X., Petty, S. J. & MacKinnon, J. L. Cyclic dynamics in field vole populations and generalist predation. J. Anim. Ecol. 69, 106–118 (2000).

    Article  Google Scholar 

  22. Lambin, X., Elston, D., Petty, S. & MacKinnon, J. Spatial patterns and periodic travelling waves in cyclic field vole, Microtus agrestis, populations. Proc. R. Soc. Lond. B 265, 1491–1496 (1998).

    Article  CAS  Google Scholar 

  23. Nelson, R. J. Photoperiod-nonresponsive morphs: a possible variable in microtine population-density fluctuations. Am. Nat. 130, 350–369 (1987).

    Article  Google Scholar 

  24. Nichols, J. D. Capture recapture models; using marked animals to study population dynamics. BioScience 42, 94–102 (1992).

    Article  Google Scholar 

  25. Lebreton, J.-D., Burnham, K. P., Clobert, J. & Anderson, D. R. Modeling survival and testing biological hypotheses using marked animals: a unified approach with case studies. Ecol. Monogr. 62, 67–118 (1992).

    Article  Google Scholar 

  26. Burnham, K. P. & Anderson, D. R. Model Selection and Inference: a Practical Information-Theoretic Approach (Springer, New York, 1998).

    Book  Google Scholar 

  27. Kendall, W. L., Pollock, K. H. & Brownie, C. A likelihood-based approach to capture-recapture estimation of demographic parameters under the robust design. Biometrics 51, 293–308 (1995).

    Article  CAS  Google Scholar 

  28. Littell, R. C., Milliken, G. A., Stroup, W. W. & Wolfinger, R. D. SAS Systems for Mixed Models (SAS Institute, Cary, North Carolina, 1996).

    Google Scholar 

Download references

Acknowledgements

The project was funded by grants from the Norwegian Research Council to T.E. and by the Natural Environment Research Council (UK) to X.L. We thank the Forestry Commission for support; C. Griffin and J. Aars for assistance during the transplant; and R. Boonstra, L. Crespin, K. E. Hodges, R. A. Ims, R. Julliard, T. Klemola, P. Thompson, E. Tkadlec, H. Viljugrein and N. G. Yoccoz for constructive comments and advice.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Nils Chr. Stenseth.

Supplementary information

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ergon, T., Lambin, X. & Stenseth, N. Life-history traits of voles in a fluctuating population respond to the immediate environment. Nature 411, 1043–1045 (2001). https://doi.org/10.1038/35082553

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/35082553

This article is cited by

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing