Skip to main content
Genetics logoLink to Genetics
. 1992 May;131(1):155–161. doi: 10.1093/genetics/131.1.155

Heritable Variation for Sex Ratio under Environmental Sex Determination in the Common Snapping Turtle (Chelydra Serpentina)

F J Janzen 1
PMCID: PMC1204949  PMID: 1592234

Abstract

The magnitude of quantitative genetic variation for primary sex ratio was measured in families extracted from a natural population of the common snapping turtle (Chelydra serpentina), which possesses temperature-dependent sex determination (TSD). Eggs were incubated at three temperatures that produced mixed sex ratios. This experimental design provided estimates of the heritability of sex ratio in multiple environments and a test of the hypothesis that genotype X environment (G X E) interactions may be maintaining genetic variation for sex ratio in this population of C. serpentina. Substantial quantitative genetic variation for primary sex ratio was detected in all experimental treatments. These results in conjunction with the occurrence of TSD in this species provide support for three critical assumptions of Fisher's theory for the microevolution of sex ratio. There were statistically significant effects of family and incubation temperature on sex ratio, but no significant interaction was observed. Estimates of the genetic correlations of sex ratio across environments were highly positive and essentially indistinguishable from +1. These latter two findings suggest that G X E interaction is not the mechanism maintaining genetic variation for sex ratio in this system. Finally, although substantial heritable variation exists for primary sex ratio of C. serpentina under constant temperatures, estimates of the effective heritability of primary sex ratio in nature are approximately an order of magnitude smaller. Small effective heritability and a long generation time in C. serpentina imply that evolution of sex ratios would be slow even in response to strong selection by, among other potential agents, any rapid and/or substantial shifts in local temperatures, including those produced by changes in the global climate.

Full Text

The Full Text of this article is available as a PDF (781.5 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Erickson J. W., Cline T. W. Molecular nature of the Drosophila sex determination signal and its link to neurogenesis. Science. 1991 Mar 1;251(4997):1071–1074. doi: 10.1126/science.1900130. [DOI] [PubMed] [Google Scholar]
  2. Harry J. L., Briscoe D. A. Multiple paternity in the loggerhead turtle (Caretta caretta). J Hered. 1988 Mar-Apr;79(2):96–99. doi: 10.1093/oxfordjournals.jhered.a110480. [DOI] [PubMed] [Google Scholar]
  3. Janzen F. J., Paukstis G. L. Environmental sex determination in reptiles: ecology, evolution, and experimental design. Q Rev Biol. 1991 Jun;66(2):149–179. doi: 10.1086/417143. [DOI] [PubMed] [Google Scholar]
  4. Mousseau T. A., Roff D. A. Natural selection and the heritability of fitness components. Heredity (Edinb) 1987 Oct;59(Pt 2):181–197. doi: 10.1038/hdy.1987.113. [DOI] [PubMed] [Google Scholar]
  5. Orzack S. H., Parker E. D., Jr Genetic variation for sex ratio traits within a natural population of a parasitic wasp, Nasonia vitripennis. Genetics. 1990 Feb;124(2):373–384. doi: 10.1093/genetics/124.2.373. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Orzack S. H. The comparative biology of second sex ratio evolution within a natural population of a parasitic wasp, Nasonia vitripennis. Genetics. 1990 Feb;124(2):385–396. doi: 10.1093/genetics/124.2.385. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Parker E. D., Jr, Orzack S. H. Genetic variation for the sex ratio in Nasonia vitripennis. Genetics. 1985 May;110(1):93–105. doi: 10.1093/genetics/110.1.93. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Genetics are provided here courtesy of Oxford University Press

RESOURCES