Skip to main content
Proceedings of the Royal Society B: Biological Sciences logoLink to Proceedings of the Royal Society B: Biological Sciences
. 2000 Feb 22;267(1441):371–377. doi: 10.1098/rspb.2000.1011

Extreme environmental change and evolution: stress-induced morphological variation is strongly concordant with patterns of evolutionary divergence in shrew mandibles.

A V Badyaev 1, K R Foresman 1
PMCID: PMC1690536  PMID: 10722219

Abstract

Morphological structures often consist of simpler traits which can be viewed as either integrated (e.g. correlated due to functional interdependency) or non-integrated (e.g. functionally independent) traits. The combination of a long-term stabilizing selection on the entire structure with a short-term directional selection on an adaptively important subset of traits should result in long historical persistence of integrated functional complexes, with environmentally induced variation and macroevolutionary change confined mostly to non-integrated traits. We experimentally subjected populations of three closely related species of Sorex shrews to environmental stress. As predicted, we found that most of the variation in shrew mandibular shape was localized between rather than within the functional complexes; the patterns of integration did not change between the species. The stress-induced variation was confined to nonintegrated traits and was highly concordant with the patterns of evolutionary change--species differed in the same set of non-integrated traits which were most sensitive to stress within each species. We suggest that low environmental and genetic canalization of non-integrated traits may have caused these traits to be most sensitive not only to the environmental but also to genetic perturbations associated with stress. The congruence of stress-induced and between-species patterns of variation in non-integrated traits suggests that stress-induced variation in these traits may play an important role in species divergence.

Full Text

The Full Text of this article is available as a PDF (239.0 KB).

Selected References

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

  1. Björklund M. Species selection on organismal integration. J Theor Biol. 1994 Dec 21;171(4):427–430. doi: 10.1006/jtbi.1994.1246. [DOI] [PubMed] [Google Scholar]
  2. Cheverud J. M. Quantitative genetics and developmental constraints on evolution by selection. J Theor Biol. 1984 Sep 21;110(2):155–171. doi: 10.1016/s0022-5193(84)80050-8. [DOI] [PubMed] [Google Scholar]
  3. Churchill S. E. Particulate versus integrated evolution of the upper body in late pleistocene humans: a test of two models. Am J Phys Anthropol. 1996 Aug;100(4):559–583. doi: 10.1002/(SICI)1096-8644(199608)100:4<559::AID-AJPA9>3.0.CO;2-L. [DOI] [PubMed] [Google Scholar]
  4. Fumagalli L., Taberlet P., Stewart D. T., Gielly L., Hausser J., Vogel P. Molecular phylogeny and evolution of Sorex shrews (Soricidae: insectivora) inferred from mitochondrial DNA sequence data. Mol Phylogenet Evol. 1999 Mar;11(2):222–235. doi: 10.1006/mpev.1998.0568. [DOI] [PubMed] [Google Scholar]
  5. Lande R. The Genetic Covariance between Characters Maintained by Pleiotropic Mutations. Genetics. 1980 Jan;94(1):203–215. doi: 10.1093/genetics/94.1.203. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Lande R. The genetic correlation between characters maintained by selection, linkage and inbreeding. Genet Res. 1984 Dec;44(3):309–320. doi: 10.1017/s0016672300026549. [DOI] [PubMed] [Google Scholar]

Articles from Proceedings of the Royal Society B: Biological Sciences are provided here courtesy of The Royal Society

RESOURCES