Skip to main content
Log in

Adaptive plasticity of egg size in response to competition in the cowpea weevil, Callosobruchus maculatus (Coleoptera: Bruchidae)

  • Original Paper
  • Published:
Oecologia Aims and scope Submit manuscript

Abstract

Life history theory predicts that larger propagules should be produced when the offspring are expected to experience intense competition. This study tested whether female cowpea weevils responded to high larval or adult density by producing larger eggs. In a splitbrood design I measured the effect of density experienced by females at their larval stage (1 vs. 4–6 larvae/cowpea) on the size of eggs produced just after emergence. The females were then kept either at low adult density (1 female+1 male per vial), or at high adult density (10 females+10 males) for 2 days, and tested for the effect of this adult density treatment on the size of eggs laid subsequently. I measured egg length and width, as well as the diameter of the entrance tunnel made by the larva, which can be regarded as a crude measure of larval size. Females that experienced high adult density subsequently laid slightly wider eggs than those kept at low density. This difference, albeit small (about 1–4% after correction for female weight and the effect of family, depending on the statistical model used), was statistically significant and robust to alterations of the statistical model. It may be a remnant of a larger plastic response of egg size to competition that has become eroded during many generations in high-density laboratory cultures. There was no difference in egg length or the diameter of the entrance tunnel. Eggs laid just after emergence by females reared at high larval density also tended to be wider than those produced by females that had no competitors. This effect was only marginally significant, however, and sensitive to the statistical model. Both egg length and width and the diameter of the entrance tunnel increased with female weight and decreased with female age. The tunnel diameter was positively correlated with both egg length and width, but the effect of width was larger.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Begon M, Parker GA (1986) Should egg size and clutch size decrease with age? Oikos 47:293–302

    Google Scholar 

  • Duellman WE, Trueb L (1986) Biology of amphibians. McGraw-Hill, New York

    Google Scholar 

  • Fox CW (1993) The influence of maternal age and mating frequency on egg size and offspring performance in Callosobruchus maculatus (Coleoptera: Bruchidae). Oecologia 96:139–146

    Google Scholar 

  • Giga DP, Smith RH (1985) Oviposition markers in Callosobruchus maculatus F. and Callosobruchus rhodesianus Pic. (Coleoptera, Bruchidae): asymmetry of interspecific responses. Agric Ecosyst Environ 12:229–233

    Google Scholar 

  • Kawecki TJ (1993) Age and size at maturity in a patchy environment: fitness maximization versus evolutionary stability. Oikos 66:309–317

    Google Scholar 

  • King DA (1990) The adaptive significance of tree height. Am Nat 135:809–828

    Google Scholar 

  • Mäkela A (1985) Differential games in evolutionary theory: height growth strategies of trees. Theor Popul Biol 27:239–267

    Google Scholar 

  • Maynard Smith J, Brown RL (1986) Competition and body size. Theor Popul Biol 30:166–179

    Google Scholar 

  • McLachlan AJ (1989) Animal populations and extreme densities: size dimorphism by frequency-dependent selection in ephemeral habitats. Funct Ecol 3:633–637

    Google Scholar 

  • Messina FJ (1991) Life-history variation in a seed beetle: adult egg-laying vs. larval competitive ability. Oecologia 85:447–455

    Google Scholar 

  • Mirmirani M, Oster G (1978) Competition, kin selection, and evolutionary stable strategies. Theor Popul Biol 13:304–339

    Google Scholar 

  • Møller H, Smith RH, Sibly RM (1989) Evolutionary demography of a bruchid beetle. I. Quantitative genetical analysis of the female life history. Funct Ecol 3:673–681

    Google Scholar 

  • Orton RA, Sibly RM (1990) Egg size and growth rate in Theodoxus fluviatilis (L.). Funct Ecol 4:91–94

    Google Scholar 

  • Parker GA, Begon M (1986) Optimal egg size and clustch size: effects of environment and maternal phenotype. Am Nat 128:573–592

    Google Scholar 

  • Perrin N (1989) Population density and offspring size in the cladoceran Simocephalus vetulus (Muller). Funct Ecol 3:29–36

    Google Scholar 

  • Reznick D, Endler JA (1982) The impact of predation on life history evolution in Trinidadian guppies (Poecilia reticulata). Evolution 36:160–177

    Google Scholar 

  • Roff DA (1992) The evolutions of life histories. Chapman and Hall, New York

    Google Scholar 

  • SAS Institute (1980) SAS/STAT user's guide, version 6 edn. SAS Institute, Cary

    Google Scholar 

  • Sibly RM, Calow P (1983) An integrated approach to life-cycle evolution using selective landscapes. J Theor Biol 102:527–547

    Google Scholar 

  • Sibly R, Calow P, Smith RH (1988) Optimal size in seasonal breeders. J Theor Biol 133:13–21

    Google Scholar 

  • Smith CC, Fretwell SD (1974) The optimal balance between size and number of offspring. Am Nat 108:499–506

    Google Scholar 

  • Smith FE (1963) Population dynamics in Daphnia magna and a new model for population growth. Ecology 44:651–663

    Google Scholar 

  • Sokal RR, Rohlf FJ (1969) Biometry Freeman, San Francisco

    Google Scholar 

  • Stearns SC, (1992) The evolution of life histories. Oxford University Press, Oxford

    Google Scholar 

  • Visser ME, Alphen JJM van, Nell HW (1990) Adaptive superparasitism and patch time allocation in solitary parasitoids: the influence of the number of parasitoids depleting a patch. Behaviour 114:21–36

    Google Scholar 

  • Wilson K, Hill L (1989) Factors affecting egg maturation in the bean weevil Callosobruchus maculatus. Physiol Entomol 14:115–126

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kawecki, T.J. Adaptive plasticity of egg size in response to competition in the cowpea weevil, Callosobruchus maculatus (Coleoptera: Bruchidae). Oecologia 102, 81–85 (1995). https://doi.org/10.1007/BF00333313

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00333313

Key words

Navigation