Skip to main content
Log in

Selection Response Decomposition (SRD): A New Tool for Dissecting Differences and Similarities Between Matrices

  • Tools and Techniques
  • Published:
Evolutionary Biology Aims and scope Submit manuscript

An Erratum to this article was published on 06 July 2012

Abstract

Genetic and phenotypic variance/covariance matrices are a fundamental measure of the amount of variation and the pattern of association among traits for current investigations in evolutionary biology. Still, few methods have been developed to accomplish the goal of pinpointing in which traits two matrices differ most, hampering further works on the field. We here described a novel method for dissecting matrix comparisons. This method is called Selection Response Decomposition and is an extension of the random skewers in the sense that evolutionary responses produced by known simulated selection vectors are unfolded and then compared in terms of the direct and indirect responses to selection for any trait. We also applied the method in diverse case studies, illustrating its potential. Both theoretical matrices and empirical biological data were used in the comparisons made. In the theoretical ones, the method was able to determine exactly which traits were responsible for the known a priori differences between the matrices, as well as where matrices remained similar to each other. Similar support could be observed in comparisons carried on between matrices produced from empirical biological data, since reasonable and detailed interpretations could be made regarding matrix comparisons. SRD represents an excellent tool for matrix comparisons and should provide quantitative evolutionary biology with a new method for analyzing and comparing variance/covariance patterns.

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.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8
Fig. 9
Fig. 10

Similar content being viewed by others

References

  • Abdala, F., Flores, D., & Giannini, N. P. (2001). Postweaning ontogeny of the skull of Didelphis albiventris. Journal of Mammalogy, 82, 190–200.

    Article  Google Scholar 

  • Arnold, S. J. (2005). The utlimate causes of phenotypic integration: Lost in translation (Book Review). Evolution, 59, 2059–2061.

    Google Scholar 

  • Arnold, S. J., Pfrender, M. E., & Jones, A. G. (2001). The adaptive landscape as a conceptual bridge between micro- and macroevolution. Genetica, 112(113), 9–32.

    Article  PubMed  Google Scholar 

  • Cheverud, J. M. (1982). Relationships among ontogenetic, static, and evolutionary allometry. American Journal of Physical Anthropology, 59, 139–149.

    Article  PubMed  CAS  Google Scholar 

  • Cheverud, J. M. (1988). A comparison of genetic and phenotypic correlations. Evolution, 42, 958–968.

    Article  Google Scholar 

  • Cheverud, J. M. (1995). Morphological integration in the saddle-back tamarin (Saguinus fuscicollis) cranium. The American Naturalist, 145, 63–89.

    Article  Google Scholar 

  • Cheverud, J. M. (1996). Quantitative genetic analysis of cranial morphology in the cotton-top (Saguinus oedipus) and saddle-back (S. fuscicolis) tamarins. Journal of Evolutionary Biology, 9, 5–42.

    Article  Google Scholar 

  • Cheverud, J. M., & Marroig, G. (2007). Comparing covariance matrices: Random skewers method compared to the common principal components model. Genetics and Molecular Biology, 30, 461–469.

    Article  Google Scholar 

  • Cowley, D. E., & Achtley, W. R. (1992). Comparison of quantitative genetic parameters. Evolution, 46, 1965–1967.

    Article  Google Scholar 

  • Falconer, D. S., & Mackay, T. F. C. (1996). Introduction to quantitative genetics (4th ed.). New York: Longman.

    Google Scholar 

  • Houle, D., Mezey, J., & Galpern, P. (2002). Interpretation of the results of common principal components analyses. Evolution, 56, 433–440.

    PubMed  Google Scholar 

  • Krzanowski, W. J. (1979). Between-group comparisons of principal components. Journal of the American Statistical Association, 74, 703–707.

    Article  Google Scholar 

  • Lande, R. (1979). Quantitative genetic-analysis of multivariate evolution, applied to brain—body size allometry. Evolution, 33, 402–416.

    Article  Google Scholar 

  • Lush, J. L. (1964). Melhoramento genético dos animais domésticos. Rio de Janeiro: Sedegra.

    Google Scholar 

  • Lynch, M., & Walsh, J. B. (1998). Genetics and analysis of quantitative traits. Sunderland, MA: Sinauer Assocs., Inc.

    Google Scholar 

  • Marroig, G. (2007). When size makes a difference: allometry, life-history and morphological evolution of capuchins (Cebus) and squirrels (Saimiri) monkeys (Cebinae, Platyrrhini). BMC Evolutionary Biology, 7, 7–20.

    Article  Google Scholar 

  • Marroig, G., & Cheverud, J. M. (2001). A comparison of phenotypic variation and covariation patterns and the role of phylogeny, ecology, and ontogeny during cranial evolution of new world monkeys. Evolution, 55, 2576–2600.

    PubMed  CAS  Google Scholar 

  • Marroig, G., & Cheverud, J. M. (2010). Size as a line of least resistance II: Direct selection on size or correlated response due to constraints? Evolution, 64, 1470–1488.

    PubMed  Google Scholar 

  • Phillips, P. C., & Arnold, S. J. (1999). Hierarchical comparison of genetic variance-covariance matrices. I. Using the Flury hierarchy. Evolution, 53, 1506–1515.

    Article  Google Scholar 

  • Porto, A., Oliveira, F. B., Shirai, L. T., Conto, V., & Marroig, G. (2009). The evolution of modularity in the mammalian skull I: Morphological integration patterns and magnitudes. Evolutionary Biology, 36, 118–135.

    Article  Google Scholar 

  • Roff, D. A. (1997). Evolutionary quantitative genetics. New York: Chapman & Hall.

    Book  Google Scholar 

  • Shaw, R. G. (1987). Maximum-likelihood approaches applied to quantitative genetics of natural populations. Evolution, 41, 812–826.

    Article  Google Scholar 

  • Shirai, L. T., & Marroig, G. (2010). Skull modularity in neotropical marsupials and monkeys: Size variation and evolutionary constraint and flexibility. Journal of Experimental Zoology (Mol. Dev. Evol.).

  • Smith, K. K. (1996). Integration of craniofacial structures during development in mammals. American Zoologist, 36, 70–79.

    Google Scholar 

  • Smith, K. K. (1997). Comparative patterns of craniofacial development in eutherian and metatherian mammals. Evolution, 51, 1663–1678.

    Article  Google Scholar 

  • Smith, K. K. (2001). The evolution of mammalian development. Bulletin of the Museum of Comparative Zoology, 156, 119–135.

    Google Scholar 

  • Sokal, R. R., & Braumann, C. A. (1980). Significance tests for coefficients of variation and variability profiles. Systematic Zoology, 29, 50–66.

    Article  Google Scholar 

  • Steppan, S. J., Phillips, P. C., & Houle, D. (2002). Comparative quantitative genetics: Evolution of the G matrix. Trends in Ecology & Evolution, 17, 320–327.

    Article  Google Scholar 

  • Tyndale-Biscoe, C. H., & Mackenzie, R. B. (1976). Reproduction in Didelphis marsupialis and D. albiventris in Colombia. Journal of Mammalogy, 57, 249–265.

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

To those people and institutions who provided generous help and access to collections: R. Voss, E. Westwig, and A. Fleming (AMNH); L. Gordon (NMNH); J. Patton, E. Lacey, and C. Conroy (MVZ); B. Patterson and B. Stanley (FMNH). We also express our gratitude to both reviewers and the several insightful comments on a earlier version of the manuscript. Financial support was provided by Fundação de Amparo a Pesquisa do Estado de São Paulo—FAPESP, Coordenadoria de Aperfeiçoamento de Pessoal de Nível Superior—CAPES, and Museum of Vertebrate Zoology “Visiting Schoolarship”, Conselho Nacional de Desenvolvimento Científico e Tecnológico—CNPq.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Gabriel Marroig.

Additional information

An erratum to this article can be found at http://dx.doi.org/10.1007/s11692-012-9192-5

Electronic supplementary material

Rights and permissions

Reprints and permissions

About this article

Cite this article

Marroig, G., Melo, D., Porto, A. et al. Selection Response Decomposition (SRD): A New Tool for Dissecting Differences and Similarities Between Matrices. Evol Biol 38, 225–241 (2011). https://doi.org/10.1007/s11692-010-9107-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11692-010-9107-2

Keywords

Navigation