Abstract
In some species of self-fertile pulmonate snails, two sexual morphs co-occur in natural populations: regular individuals and aphallic individuals that cannot transmit sperm to other snails. Purely aphallic populations therefore reproduce obligatorily by selfing. Understanding the evolution of aphally and selfing in these snails requires a precise knowledge of phally determination. In this paper, we investigate the genetic and environmental determination of aphally in Bulinus truncatus by a survey of the family (offspring) aphally ratio of 233 individuals originating from seven natural populations and a study of the reaction norm of the family aphally ratio to temperature using 60 individuals from 10 selfed lineages of one population. Our results indicate a high genetic variability for the determination of aphally between populations and within some populations, associated with a high level of genetic determination. Our second experiment indicates a significant temperature and lineage effect though no interaction between these two effects. We discuss our results in the framework of threshold models developed for dimorphic traits with polygenic inheritance. We propose that the sexual morph of an individual at a given temperature is determined by a temperature threshold value depending on both the individual genotype and probabilistic processes.
Full Text
The Full Text of this article is available as a PDF (887.2 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Barton N. H., Turelli M. Evolutionary quantitative genetics: how little do we know? Annu Rev Genet. 1989;23:337–370. doi: 10.1146/annurev.ge.23.120189.002005. [DOI] [PubMed] [Google Scholar]
- Charnov E. L., Bull J. When is sex environmentally determined? Nature. 1977 Apr 28;266(5605):828–830. doi: 10.1038/266828a0. [DOI] [PubMed] [Google Scholar]
- Conover D. O., Heins S. W. Adaptive variation in environmental and genetic sex determination in a fish. Nature. 1987 Apr 2;326(6112):496–498. doi: 10.1038/326496a0. [DOI] [PubMed] [Google Scholar]
- Crews D., Bergeron J. M., Bull J. J., Flores D., Tousignant A., Skipper J. K., Wibbels T. Temperature-dependent sex determination in reptiles: proximate mechanisms, ultimate outcomes, and practical applications. Dev Genet. 1994;15(3):297–312. doi: 10.1002/dvg.1020150310. [DOI] [PubMed] [Google Scholar]
- Dempster E. R., Lerner I. M. Heritability of Threshold Characters. Genetics. 1950 Mar;35(2):212–236. doi: 10.1093/genetics/35.2.212. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gouyon P. H., Couvet D. A conflict between two sexes, females and hermaphrodites. Experientia Suppl. 1987;55:245–261. doi: 10.1007/978-3-0348-6273-8_11. [DOI] [PubMed] [Google Scholar]
- Hazel W. N., Smock R., Johnson M. D. A polygenic model for the evolution and maintenance of conditional strategies. Proc Biol Sci. 1990 Dec 22;242(1305):181–187. doi: 10.1098/rspb.1990.0122. [DOI] [PubMed] [Google Scholar]
- Janzen F. J. Heritable variation for sex ratio under environmental sex determination in the common snapping turtle (Chelydra serpentina). Genetics. 1992 May;131(1):155–161. doi: 10.1093/genetics/131.1.155. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jarne P., Viard F., Delay B., Cuny G. Variable microsatellites in the highly selfing snail Bulinus truncatus (Basommatophora: Planorbidae). Mol Ecol. 1994 Oct;3(5):527–528. doi: 10.1111/j.1365-294x.1994.tb00132.x. [DOI] [PubMed] [Google Scholar]
- Robertson A., Lerner I. M. The Heritability of All-or-None Traits: Viability of Poultry. Genetics. 1949 Jul;34(4):395–411. doi: 10.1093/genetics/34.4.395. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Roff D. A. The evolution of dimorphic traits: predicting the genetic correlation between environments. Genetics. 1994 Jan;136(1):395–401. doi: 10.1093/genetics/136.1.395. [DOI] [PMC free article] [PubMed] [Google Scholar]
