2010
DOI: 10.1111/j.1365-294x.2010.04698.x
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Back to nature: ecological genomics of loblolly pine (Pinus taeda, Pinaceae)

Abstract: Genetic variation is often arrayed in latitudinal or altitudinal clines, reflecting either adaptation along environmental gradients, migratory routes, or both. For forest trees, climate is one of the most important drivers of adaptive phenotypic traits. Correlations of single and multilocus genotypes with environmental gradients have been identified for a variety of forest trees. These correlations are interpreted normally as evidence of natural selection. Here, we use a genome-wide dataset of single nucleotid… Show more

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Cited by 196 publications
(218 citation statements)
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“…This proportion of candidate loci is similar to that found in a previous study (2.7%) in which 148 cleaved amplified polymorphic sequence loci were examined (Tsumura et al, 2007). Eckert et al (2010) identified 22 candidate loci (BF log 10 42.0) associated with climate variables from 1730 loci in 682 loblolly pine tree samples covering the full range of the species. Prunier et al (2011) also identified 10 candidate loci above 99% confidence interval in black spruce.…”
Section: Detection Of Outlier Locisupporting
confidence: 69%
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“…This proportion of candidate loci is similar to that found in a previous study (2.7%) in which 148 cleaved amplified polymorphic sequence loci were examined (Tsumura et al, 2007). Eckert et al (2010) identified 22 candidate loci (BF log 10 42.0) associated with climate variables from 1730 loci in 682 loblolly pine tree samples covering the full range of the species. Prunier et al (2011) also identified 10 candidate loci above 99% confidence interval in black spruce.…”
Section: Detection Of Outlier Locisupporting
confidence: 69%
“…Although LD in forest trees decays rapidly within several thousand basepairs (Neale and Savolainen, 2004), Eckert et al (2010) have observed high LD in the loblolly pine, affecting the set of five SNPs located on LG 8. The LD of forest trees has to date only been estimated in coding regions; it is possible that the LD values of non-coding regions might be higher than those for coding regions, as is the case in angiosperms (Gaut et al, 2007;Moritsuka et al, 2012).…”
Section: Relationships With Environmental Variablesmentioning
confidence: 99%
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“…These climatic variables could be important drivers of local adaptation as phenotypic traits such as timing of budburst, timing of budset (or growth initiation and cessation), and cold hardiness vary significantly among populations of both species (Joyce & Rehfeldt, 2013; Joyce & Sinclair, 2002; Li et al., 1997; Lu et al., 2003a,b; Rehfeldt et al., 1984). The putative ortholog (i.e., gene amplified using the same primers as those used in this study) was also detected as an F ST outlier among environmental groups defined based on DD5 in June and precipitation in December in Larix decidua (Mosca et al., 2013), and associated with spring–fall precipitation and aridity in P. taeda (Eckert et al., 2010). Thus, this gene may have evolved in response to climatic constraints in multiple tree species.…”
Section: Discussionmentioning
confidence: 99%
“…Despite the advantages of common garden experiments, the study of local adaptation in non-model species during the past decade has been strongly driven by the study of genetic markers in natural populations (Luikart et al, 2003). Typically, evolutionary biologists go to natural populations, sample tissue from the individuals and genotype them with high-throughput methods and then proceed with a genome scan analysis of selection (see, for example, Eckert et al, 2010;Bourret et al, 2013;Fischer et al, 2013). Although this method can be quite powerful, it has some limitations (for example, false positives, no information on the adaptive phenotype).…”
Section: Introductionmentioning
confidence: 99%