Abstract

Populations often contain discrete classes or morphs (e.g., sexual dimorphisms, wing dimorphisms, trophic dimorphisms) characterized by distinct patterns of trait expression. In quantitative genetic analyses, the different morphs can be considered as different environments within which traits are expressed. Genetic variances and covariances can then be estimated independently for each morph or in a combined analysis. In the latter case, morphs can be considered as separate environments in a bivariate analysis or entered as fixed effects in a univariate analysis. Although a common approach, we demonstrate that the latter produces downwardly biased estimates of additive genetic variance and heritability unless the quantitative genetic architecture of the traits concerned is perfectly correlated between the morphs. This result is derived for four widely used quantitative genetic variance partitioning methods. Given that theory predicts the evolution of genotype-by-environment (morph) interactions as a consequence of selection favoring different trait combinations in each morph, we argue that perfect correlations between the genetic architectures of the different morphs are unlikely. A sampling of the recent literature indicates that the majority of researchers studying traits expressed in different morphs recognize this and do estimate morph-specific quantitative genetic architecture. However, ca. 16% of the studies in our sample utilized only univariate, fixed-effects models. We caution against this approach and recommend that it be used only if supported by evidence that the genetic architectures of the different morphs do not differ.

Highlights

  • The fundamentals of quantitative genetics (Fisher 1918) provide the theoretical foundation for most of evolutionary ecology (Kruuk et al 2008) and the adoption of quantitative genetic methods in evolutionary ecology research enables us to make quantitative predictions about the rate and direction of phenotypic evolution (Wilson et al 2010)

  • Recent work has highlighted other contributions to phenotypic variance, such as common environment, maternal genetic, and spatial autocorrelation among relatives (Kruuk et al 2001; MacColl and Hatchwell 2003; Charmantier et al 2004; Wilson et al 2005; Kruuk and Hadfield 2007; Stopher et al 2012), estimates of additive genetic variance are of paramount importance for predicting population responses to natural selection (Kruuk et al 2008) using the breeder’s equation (Falconer 1989; Lynch and Walsh 1998) or the Secondary Theorem of Natural Selection (Robertson 1966; Price 1970)

  • Estimates of additive genetic variance are at the heart of many studies in evolutionary ecology that are conducted to answer general questions regarding (1) the evolutionary forces that shape additive variance; and (2) population responses to selection

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Summary

Introduction

The fundamentals of quantitative genetics (Fisher 1918) provide the theoretical foundation for most of evolutionary ecology (Kruuk et al 2008) and the adoption of quantitative genetic methods in evolutionary ecology research enables us to make quantitative predictions about the rate and direction of phenotypic evolution (Wilson et al 2010). Methods of estimating the additive genetic variance (i.e., the variance in breeding values) from the covariance between offspring and parents, or the variance among half-sib families depend on there being no genotypeby-morph interaction for breeding values expressed in two different morphs (in addition to other assumptions regarding random mating, nonadditive genetic effects, and inbreeding; Falconer 1989; Lynch and Walsh 1998).

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