Climate change has the potential to affect the ecology and evolution of every species on Earth. Although the ecological consequences of climate change are increasingly well documented, the effects of climate on the key evolutionary process driving adaptationnatural selection-are largely unknown. We report that aspects of precipitation and potential evapotranspiration, along with the North Atlantic Oscillation, predicted variation in selection across plant and animal populations throughout many terrestrial biomes, whereas temperature explained little variation. By showing that selection was influenced by climate variation, our results indicate that climate change may cause widespread alterations in selection regimes, potentially shifting evolutionary trajectories at a global scale.C limate affects organisms in ways that ultimately shape patterns of biodiversity (1). Consequently, the rapid changes in Earth's recent climate impose challenges for many organisms, often reducing population fitness (2-4). Although some species may migrate and undergo range shifts to avoid climate-induced declines and potential extinction (5), an alternative outcome is adaptive evolution in response to selection imposed by climate (6). However, we lack a general understanding of whether local and global climatic factors such as temperature, precipitation, and water availability influence selection (2, 7). Understanding these effects is critical for predicting the consequences of increasing droughts, heat waves, and extreme precipitation events that are expected in many regions (8, 9).To quantify how climate variation influences selection, we assembled a large database of standardized directional selection gradients and differentials from spatially [mean = 4.6 ± 5.4 (SD) populations, range = 2 to 59 populations] and temporally [mean = 5.2 ± 6.8 (SD) years, range = 2 to 45 years] replicated selection studies (N = 168) in plant and animal populations (Table 1 and database S1). We focused on directional selection that can generate increases or decreases in trait values because it is well characterized and is likely to drive rapid evolution (10) in response to variation in climatic factors. However, selection acting on trait combinations and trait variance may also be affected by climate (7). Selection gradients estimate the strength and direction of selection acting directly on a trait, whereas differentials estimate "total selection" on a trait via both direct and indirect selection because of trait correlations (11). These standardized selection coefficients describe selection in terms of the relationship between relative fitness and quantitative traits measured in standard deviations, thus facilitating cross-study comparisons (11,12).Geographically, the database contains many estimates of selection from temperate, mid-latitude regions centered at 40°N (Fig. 1A). The populations in this database span many terrestrial biomes on Earth, with the exception of tundra and tropical rainforests where selection has rarely been quantified (Fig. 1B...
Floral traits are hypothesized to evolve primarily in response to selection by pollinators. However, selection can also be mediated by other environmental factors. To understand the relative importance of pollinator‐mediated selection and its variation among trait and pollinator types, we analyzed directional selection gradients on floral traits from experiments that manipulated the environment to identify agents of selection. Pollinator‐mediated selection was stronger than selection by other biotic factors (e.g., herbivores), but similar in strength to selection by abiotic factors (e.g., soil water), providing partial support for the hypothesis that floral traits evolve primarily in response to pollinators. Pollinator‐mediated selection was stronger on pollination efficiency traits than on other trait types, as expected if efficiency traits affect fitness via interactions with pollinators, but other trait types also affect fitness via other environmental factors. In addition to varying among trait types, pollinator‐mediated selection varied among pollinator taxa: selection was stronger when bees, long‐tongued flies, or birds were the primary visitors than when the primary visitors were Lepidoptera or multiple animal taxa. Finally, reducing pollinator access to flowers had a relatively small effect on selection on floral traits, suggesting that anthropogenic declines in pollinator populations would initially have modest effects on floral evolution.
Although rarely tested, it is often assumed that interspecific competition results in the divergence of traits related to resource use. Using a plant-pollinator system as a model, I tested the prediction the presence of a competitor for pollination influences the strength and/or direction of pollinator-mediated selection on floral traits. I measured phenotypic selection via female fitness on five floral traits of Ipomopsis aggregata in seven populations. Four contained only conspecifics (I only) and three also contained the competitor Castilleja linariaefolia (C + I). Directional selection via fruits/plant and conspecific pollen deposited/flower on corolla length was positive and significantly stronger in C + I populations. This difference in selection was apparently driven by interpopulation variation in the degree to which reproduction of I. aggregata was pollen limited. Consistent with expectations of interspecific competition, I. aggregata plants in C + I populations received less conspecific pollen per flower and set fewer seeds per fruit and fruits per plant than those in I only populations. Ipomopsis aggregata's corollas were also significantly longer in C + I populations, suggesting that there had been a response to a similar selective regime in past generations. Phenotypic correlations between corolla length and width, which determine the variation in I. aggregata's flower shape, were significantly weaker in C + I populations. These data suggest that competition for pollination can influence the strength of selection on and patterns of correlations among floral traits of I. aggregata. If I. aggregata populations with and without competitors for pollination are linked by gene flow, then measuring selection in competitive and noncompetitive environments maybe necessary to accurately predict how floral traits will evolve.
When plants establish outside their native range, their ability to adapt to the new environment is influenced by both demography and dispersal. However, the relative importance of these two factors is poorly understood. To quantify the influence of demography and dispersal on patterns of genetic diversity underlying adaptation, we used data from a globally distributed demographic research network comprising 35 native and 18 nonnative populations of Plantago lanceolata. Species-specific simulation experiments showed that dispersal would dilute demographic influences on genetic diversity at local scales. Populations in the native European range had strong spatial genetic structure associated with geographic distance and precipitation seasonality. In contrast, nonnative populations had weaker spatial genetic structure that was not associated with environmental gradients but with higher within-population genetic diversity. Our findings show that dispersal caused by repeated, long-distance, human-mediated introductions has allowed invasive plant populations to overcome environmental constraints on genetic diversity, even without strong demographic changes. The impact of invasive plants may, therefore, increase with repeated introductions, highlighting the need to constrain future introductions of species even if they already exist in an area.
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