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Linear Discrimination, Ordination, and the Visualization of Selection Gradients in Modern Morphometrics

期刊

EVOLUTIONARY BIOLOGY
卷 38, 期 1, 页码 100-114

出版社

SPRINGER
DOI: 10.1007/s11692-011-9109-8

关键词

Canonical variate analysis; Linear discriminant function; Ordination; Principal component analysis; Procrustes; Selection gradient

资金

  1. Direct For Biological Sciences
  2. Division Of Environmental Biology [1019583] Funding Source: National Science Foundation

向作者/读者索取更多资源

Linear discriminant analysis (LDA) is a multivariate classification technique frequently applied to morphometric data in various biomedical disciplines. Canonical variate analysis (CVA), the generalization of LDA for multiple groups, is often used in the exploratory style of an ordination technique (a low-dimensional representation of the data). In the rare case when all groups have the same covariance matrix, maximum likelihood classification can be based on these linear functions. Both LDA and CVA require full-rank covariance matrices, which is usually not the case in modern morphometrics. When the number of variables is close to the number of individuals, groups appear separated in a CVA plot even if they are samples from the same population. Hence, reliable classification and assessment of group separation require many more organisms than variables. A simple alternative to CVA is the projection of the data onto the principal components of the group averages (between-group PCA). In contrast to CVA, these axes are orthogonal and can be computed even when the data are not of full rank, such as for Procrustes shape coordinates arising in samples of any size, and when covariance matrices are heterogeneous. In evolutionary quantitative genetics, the selection gradient is identical to the coefficient vector of a linear discriminant function between the populations before vs. after selection. When the measured variables are Procrustes shape coordinates, discriminant functions and selection gradients are vectors in shape space and can be visualized as shape deformations. Except for applications in quantitative genetics and in classification, however, discriminant functions typically offer no interpretation as biological factors.

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