2015
DOI: 10.1016/j.ppees.2015.02.006
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Patterns of genetic variation within and among populations in Arbutus unedo and its relation with selection and evolvability

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Cited by 18 publications
(17 citation statements)
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“…Despite the ubiquity and eco‐evolutionary implications of P × E , a considerable proportion of studies (>20%) were performed in only one test environment, which prevents its calculation (e.g., Alberto et al, ; Hernandez‐Serrano et al, ; Sebastian‐Azcona, Hacke, & Hamann, ). For instance, only one test environment is used in most studies using F ST – Q ST comparisons (e.g., Frank, Sperisen, et al, ; Hernandez‐Serrano et al, ; Santiso et al, ); Q ST measures population differentiation in functional traits, and may be compared to F ST , a metric widely used to measure population differentiation in neutral molecular markers. Their comparison informs on the role of divergent natural selection in the functional differentiation of populations (see Merilä & Crnokrak ).…”
Section: Discussionmentioning
confidence: 99%
“…Despite the ubiquity and eco‐evolutionary implications of P × E , a considerable proportion of studies (>20%) were performed in only one test environment, which prevents its calculation (e.g., Alberto et al, ; Hernandez‐Serrano et al, ; Sebastian‐Azcona, Hacke, & Hamann, ). For instance, only one test environment is used in most studies using F ST – Q ST comparisons (e.g., Frank, Sperisen, et al, ; Hernandez‐Serrano et al, ; Santiso et al, ); Q ST measures population differentiation in functional traits, and may be compared to F ST , a metric widely used to measure population differentiation in neutral molecular markers. Their comparison informs on the role of divergent natural selection in the functional differentiation of populations (see Merilä & Crnokrak ).…”
Section: Discussionmentioning
confidence: 99%
“…The additive genetic variance (σA2) was estimated as 4 × σf2, as we assumed that each offspring of a dam (maternal plant) has a different sire (pollen donor). If multiple ovules from the same plant were pollinated by the same pollen donor, then the relatedness of the offspring (replicate siblings from a given family) from the same plant would be greater than is assumed here, and the estimates of additive genetic variance would be upwardly biased (Falconer and Mackay, 1996; Santiso et al, 2015). Ninety-five percentage confidence intervals for the heritability estimates were computed using a bootstrapping approach with 1000 simulations, using the function “bootMer” in package lme4.…”
Section: Methodsmentioning
confidence: 96%
“…We also calculated the coefficient of genetic variation (CVA) as √σA2 divided by the trait mean (Houle, 1992), for traits with values only at one side of zero. This parameter provides a measure of genetic variation standardized by the mean, allowing to qualitatively comparing genetic variation among different traits (e.g., Agrawal et al, 2008; Santiso et al, 2015). Finally, to provide an index of genetically based variance, we additionally examined the proportion of phenotypic variance attributed to differences among families, as σf2/σph2, and to differences among populations, as σp2/σph2 [see (Facon et al, 2008; Matesanz et al, 2014) for other studies using these metrics as estimates of genetic variation].…”
Section: Methodsmentioning
confidence: 99%
“…All these techniques would be very useful tools for breeding programs involving Arbutus species or for developing effective conservation strategies. Santiso et al (2015) reported that A. unedo maintains the ability to evolve despite low genetic differentiation and stabilizing selection. The present study, proposing appropriate morphological characteristics in combination with selected molecular markers for distinguish individuals of three Arbutus species, is a step in achieving these goals for Arbutus spp.…”
Section: Molecular Analysismentioning
confidence: 99%