2019
DOI: 10.1111/eva.12883
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Genomic assessment of local adaptation in dwarf birch to inform assisted gene flow

Abstract: When populations of a rare species are small, isolated and declining under climate change, some populations may become locally maladapted. Detecting this maladaptation may allow effective rapid conservation interventions, even if based on incomplete knowledge. Population maladaptation may be estimated by finding genome–environment associations (GEA) between allele frequencies and environmental variables across a local species range, and identifying populations whose allele frequencies do not fit with these tre… Show more

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Cited by 49 publications
(65 citation statements)
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“…Even under a moderate future climate scenario including mitigation measures (RCP4.5), the estimated mean AF shift required for the temperature‐associated loci is at least three fold higher than the rate at which populations have shifted their AFs in the past (Figure 4a). Although the AF shift was not specifically related to time, and while climate zones are difficult to compare, previous studies looking at a predictive time‐span of 95–140 years estimated similar RONA values for a projected composite climate measure (0.05–0.48 for Betula nana ; Borrell et al, 2020) or for a projected mean temperature (0.10–0.30 for Eucalyptus microcarpa [RCP8.5; Jordan et al, 2017], 0.09–0.30 for Quercus spp. [scenario A1B; Rellstab et al, 2016], and 0.07–0.38 for Quercus suber [RCP8.5; Pina‐Martins et al, 2018]).…”
Section: Discussionmentioning
confidence: 79%
“…Even under a moderate future climate scenario including mitigation measures (RCP4.5), the estimated mean AF shift required for the temperature‐associated loci is at least three fold higher than the rate at which populations have shifted their AFs in the past (Figure 4a). Although the AF shift was not specifically related to time, and while climate zones are difficult to compare, previous studies looking at a predictive time‐span of 95–140 years estimated similar RONA values for a projected composite climate measure (0.05–0.48 for Betula nana ; Borrell et al, 2020) or for a projected mean temperature (0.10–0.30 for Eucalyptus microcarpa [RCP8.5; Jordan et al, 2017], 0.09–0.30 for Quercus spp. [scenario A1B; Rellstab et al, 2016], and 0.07–0.38 for Quercus suber [RCP8.5; Pina‐Martins et al, 2018]).…”
Section: Discussionmentioning
confidence: 79%
“…This suggests that variable selection in adaptation studies should not be done using a priori knowledge solely based on the power of a variable to predict a species' realised ecological niche. In other words, it is challenging to obtain relevant clues of selective forces at the local scale when habitat characterisation depends on ecological data from the entire species' range (but see, e.g., Borrell, Zohren, Nichols, & Buggs, 2020), especially if the study design consists of a partial sampling at its leading or rear edges (Hampe & Petit, 2005). One reason that might explain this mismatch is the temporal lag involved in the two processes; species presence can reflect rather recent events, while selection signatures are related to an evolutionary time scale, whose dimension depends, among others, on the species' generation time.…”
Section: Environmental Factors In Species Distribution Models and Environmental Association Analysesmentioning
confidence: 99%
“…longevity of tussock forming plants in the arctic, the chances for establishment of southern ecotypes in the north seem unlikely, outside of assisted gene flow or migration (Borrell et al 2020).…”
Section: Acknowledgmentsmentioning
confidence: 99%