2021
DOI: 10.1002/ece3.7938
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Potential local adaptation in populations of invasive reed canary grass (Phalaris arundinacea) across an urbanization gradient

Abstract: This is an open access article under the terms of the Creat ive Commo ns Attri bution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

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Cited by 9 publications
(4 citation statements)
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“…high levels of variability) have low sensitivity to local environmental changes compared with species that have locally adapted niches and thus high sensitivity to local environmental changes (Bennett et al, 2019). For example, variability of responses in an invasive grass enabled adaptation to urban environments (Weston et al, 2021), representing a species with low sensitivity to local change and/or a species with locally adapted populations. Quantifying the differences between interspecific variability and potential intraspecific variability (i.e.…”
Section: Introductionmentioning
confidence: 99%
“…high levels of variability) have low sensitivity to local environmental changes compared with species that have locally adapted niches and thus high sensitivity to local environmental changes (Bennett et al, 2019). For example, variability of responses in an invasive grass enabled adaptation to urban environments (Weston et al, 2021), representing a species with low sensitivity to local change and/or a species with locally adapted populations. Quantifying the differences between interspecific variability and potential intraspecific variability (i.e.…”
Section: Introductionmentioning
confidence: 99%
“…Previous studies of mutualisms have predominantly focused on plant–pollinator interactions and adaptation for only one of the interacting species (Irwin et al., 2018; Rivkin et al., 2020; Theodorou et al., 2018; but see Brans et al., 2022). Moreover, studies evaluating local adaptation in urban environments have focused primarily on adaptation to abiotic factors, such as temperature (Brans et al., 2017; Martin et al., 2021) and pollutants (Reid et al., 2016; Weston et al., 2021). Anthropogenic impacts on legume–rhizobia symbioses have been evaluated in both agricultural (Lau et al., 2022; Weese et al., 2015) and more recently in urban environments (Forrester & Ashman, 2018; Regus et al., 2017; Wendlandt et al., 2022).…”
Section: Discussionmentioning
confidence: 99%
“…Moreover, studies evaluating local adaptation in urban environments have focused primarily on adaptation to abiotic factors, such as temperature (Brans et al, 2017;Martin et al, 2021) and pollutants (Reid et al, 2016;Weston et al, 2021). Anthropogenic impacts on legume-rhizobia symbioses have been evaluated in both agricultural (Lau et al, 2022;Weese et al, 2015) and more recently in urban environments (Forrester & Ashman, 2018;Regus et al, 2017;Wendlandt et al, 2022).…”
Section: Con Clus Ionsmentioning
confidence: 99%
“…Previous studies of mutualisms have predominantly focused on plant-pollinator interactions and adaptation for only one of the interacting species (Irwin et al 2018;Theodorou et al 2018;Rivkin et al 2020; but see Brans et al 2022). Moreover, studies evaluating local adaptation in urban environments have focused primarily on adaptation to abiotic factors, such as temperature (Brans et al, 2017;Martin et al, 2021) and pollutants (N. M. Reid et al, 2016;Weston et al, 2021). Anthropogenic impacts on legume-rhizobia symbioses have been evaluated in both agricultural (Lau et al, 2022;Weese et al, 2015) and more recently in urban (Forrester & Ashman, 2018;Regus et al, 2017;Wendlandt et al, 2022) environments.…”
Section: Discussionmentioning
confidence: 99%