Through the lens of evolution, climate change is an agent of natural selection that forces populations to change and adapt, or face extinction. However, current assessments of the risk of biodiversity associated with climate change1 do not typically take into account how natural selection influences populations differently depending on their genetic makeup2. Here we make use of the extensive genome information that is available for Arabidopsis thaliana and measure how manipulation of the amount of rainfall affected the fitness of 517 natural Arabidopsis lines that were grown in Spain and Germany. This allowed us to directly infer selection along the genome3. Natural selection was particularly strong in the hot-dry location in Spain, where 63% of lines were killed and where natural selection substantially changed the frequency of approximately 5% of all genome-wide variants. A significant portion of this climate-driven natural selection of variants was predictable from signatures of local adaptation (R2 = 29–52%), as genetic variants that were found in geographical areas with climates more similar to the experimental sites were positively selected. Field-validated predictions across the species range indicated that Mediterranean and western Siberian populations—at the edges of the environmental limits of this species—currently experience the strongest climate-driven selection. With more frequent droughts and rising temperatures in Europe4, we forecast an increase in directional natural selection moving northwards from the southern end of Europe, putting many native A. thaliana populations at evolutionary risk.
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Data are available in the Supplementary Tables and Supplementary Data and are deposited in Figshare (https://doi.org/10.6084/m9.figshare.6756836 and https://doi.org/10.6084/m9.figshare.6480599). Genomes are available at http://1001genomes.org/data/GMI-MPI/releases/v3.1/. The seed collection can be obtained from the Arabidopsis Biological Resource Center (ABRC) under accession CS78942 (https://abrc.osu.edu/stocks/465820). The PLINK files for genome-wide association scans of fitness and climate are deposited in the AraGWAS Catalog (https://aragwas.1001genomes.org/; https://doi.org/10.21958/study:34).
Field data cleaning and processing scripts are available from GitHub (https://github.com/MoisesExpositoAlonso/dryAR) and Zenodo (https://doi.org/10.5281/zenodo.2583224). Plant rosette area scripts are available from GitHub (http://github.com/MoisesExpositoAlonso/hippo) and Zenodo (https://doi.org/10.5281/zenodo.1039888). Inflorescence analysis scripts are available from GitHub (http://github.com/MoisesExpositoAlonso/hitfruit) and Zenodo (https://doi.org/10.5281/zenodo.2583262). Simulations of total selection coefficients inference and population allele frequency changes are available from GitHub (https://github.com/MoisesExpositoAlonso/selectioncorrelatedgenotypes) and Zenodo (https://doi.org/10.5281/zenodo.1408095).
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We thank P. Lang, A. Hancock and T. Karasov for comments on the manuscript, and members of the Weigel and Burbano laboratories for discussions; X. Picó for advice on experimental design, I. Bezrukov for advice on image-processing replicability; and B. Mendez-Vigo, C. Alonso-Blanco, A. López Quirós, M. López Herránz and M. Ángel Mora Plaza for assistance during sowing in Madrid. This work was funded by an EMBO Short Term Fellowship (M.E.-A.), ERC Advanced Grant IMMUNEMESIS and the Max Planck Society (D.W.). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
The authors declare no competing interests.
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Peer review information Nature thanks Tom Mitchell-Olds and the other, anonymous, reviewer(s) for their contribution to the peer review of this work.
Extended data figures and tables
a, View inside the foil tunnel in Germany. b, Spatial distribution of blocks and replicates in a split block design. Two independent blocks per watering condition were set up, with four spatially separated blocks within these two blocks. The 517 genotypes were then randomized within spatial blocks. The surface area of these blocks were the size of 18 or 26 quickpot trays for replicates with a high density of plants (a small population was grown per pot) or low density of plants (individual plants were grown per pot), respectively. In total, we placed 346 quickpot trays in Spain and 346 in Germany. Each quickpot tray had 40 cells of which 36 were used to sow plants (the corners were excluded). In total, 23,154 pots were successfully planted, which included about 14,500 pots with single plants (after thinning), and about 9,500 pots in which 30 seeds were planted and left to grow into small population without intervention. c, d, Soil water content (c) and soil surface temperature (d) retrieved from the 34 sensors monitoring each experimental block and the conditions outside the tunnel. Violin plots represent the distribution of recorded temperature and moisture values that were recorded every 10 min during the day and the night from three days after the day of sowing (16 November 2015 in Spain and 22 October 2015 in Germany) until the day at which all plants had completed their cycle and were dry (25 April 2016 in Spain and 15 April 2016 in Germany; n = 10,000 subsampled values of the time series). e, Set-up and examples of image-based high-throughput in situ phenotyping. (1) Customized dark box (Fotomatón) for image acquisition and (2) example tray with the corresponding green (3) and red (4) segmentation image products. Image-based monitoring was done for 23,154 pots, of which 375 pots were identified as failed replicates using the red flags placed in the field by experimenters (2 and 4). (5) Example image of a cut inflorescence of an adult plant and (6) segmentation of the inflorescence from background, (7) inflorescence path or skeletonization and (8) branch and end-point detection. In total, inflorescence images of 13,849 pots were taken and analysed. The variables extracted from inflorescence image processing (6–8) were used as predictors in a linear model that accurately estimated the number of fruits on an inflorescence, a relationship that was calibrated by manually counting fruits of small, medium and large representative plants (R2 = 0.97, n = 11, P = 10−4). a, e, All photographs were taken by M.E.-A.
a, Locations of A. thaliana accessions used in this experiment (orange), 1001 Genomes accessions (blue) and all sightings of the species in GBIF (black, https://doi.org/10.15468/dl.c3twww). b, c, Geographical origin of the 502 Eurasian native A. thaliana lines used in this study and their raw fitness data (number of offspring produced in each pot) in the experiments in Spain with low precipitation (b) and in Germany with high precipitation (c). Note the most successful genotypes in the Spanish experiment (b) come not only from central Spain, but also from other areas of the distribution with extreme climates, including north Sweden, eastern Europe, the Caucasus and Siberia, which supports our previous observations8. Note also that for the German experiment (c), there could be multiple explanations for the visual trend that lower latitude genotypes had an apparent high fitness, namely that those Mediterranean genotypes are more diverse (some with higher and some with lower fitness values than average), or that the climate in Germany during 2015–2016 favoured genotypes from warmer areas. d, e, Idealized representation of distributions of alleles associated with fitness in Spain and Germany as inferred from genome-wide environmental niche models (see Supplementary Methods I.VI). The most-significant fitness-associated SNPs (if any) in each 0.5-Mb window of the genome were modelled (n = 414 in Spain, n = 279 in Germany). Colour scale indicates the percentage of locally present alleles with respect to the maximum number of positive fitness-related alleles identified in each experiment (maps were created using R v.3.4).
Out of the A. thaliana genome matrix of 1,353,386 SNPs and 515 plants, we simulated that 1,000 randomly selected alleles were under natural selection (that is, the true selection coefficient drawn from a normal distribution around zero). Summing the selection coefficients that each of the 515 genotypes had based on their row in the genome matrix, we calculated their relative lifetime fitness. a, We then inferred the total selection coefficients s using a linear model as in Fig. 1 and compared them to the inferred estimates from a GBLUP-based genome-wide association (GWA) model (that is, a population-structure-corrected GWA), which we call direct selection coefficients in the main text (Supplementary Methods I.IV). Neither model infers the true simulated selection coefficients effectively. b, We were interested in studying the change in frequency of these 1,000 alleles after one generation of selection using individual-based simulations that sampled the genotypes for reproduction given their relative fitness. We compared the change in allele frequency in one generation (Δp = p1 − p0) with the inferred total selection coefficients and direct selection coefficients. The former, total selection coefficients, by summarizing direct and indirect effects of selection, perfectly coincide with the directionality of allele frequency changes. c, The total magnitude of allele frequency change also depends on the starting allele frequency of the allele under selection, which is described by the classic population genetics equation Δp = p(1 − p)s. Using our total selection coefficients and direct selection coefficients with this equation, we found an almost perfect relationship between predicted and realized allele frequency changes using total selection coefficients. d, To test whether the relationship in c can be extrapolated—that is, the relationship is not overly sensitive to differences in allele frequency and linkage disequilibrium in other A. thaliana subpopulations, we ran the individual-based simulations with a subset of 50 Spanish genotypes (out of the 515 genotypes) and repeated the comparison in c. The results indicate that total selection coefficients calculated from linear models are appropriate to understand the changes in allele frequencies in response to selection even when extrapolating to subpopulations with slightly different allele frequencies and linkage patterns. The regression statistics reported are: the adjusted R2, slope and regression P value, which were calculated using linear models of true compared with predicted values with n = 515. The 95% confidence interval of the regression is shaded in grey. (The code used to simulate and analyse these data can be found at https://doi.org/10.5281/zenodo.1408095.).
Manhattan plots of SNPs significantly associated with fitness, using LM-GEMMA with the relative fitness averages of the 515 genotypes and 1,353,386 SNPs in 8 different environments. SNPs that were significant after multiple comparison correction using FDR (black and grey for alternating chromosomes) or Bonferroni (red) approaches are shown. a, Analyses using only the survival fitness component. b, Analyses using only the fecundity component.
a, Conceptual workflow of field validation procedure with data from published experiments25,26. This workflow was used for Fig. 3. b, Null expectation of predictability following the workflow shown in a with datasets randomizing fitness with genotypes. We could not find any model combination that had non-zero predictability (that is, all 95% bootstrap confidence intervals overlap with zero). c, Projections of selection intensity with real datasets as in Fig. 3 using different climate change scenarios available from WorldClim (http://worldclim.org/). The higher the predicted CO2 emissions, the stronger the predicted increase in selection intensity. rcp, representative concentration pathway. d, Map of predictions of selection change in 2050 as in Fig. 3 but representing the net number of local alleles increasing or decreasing in selection Total n = 10,752 SNPs. Only changes in s of more than 5% between present and future projections were considered.
Extended Data Fig. 6 Distribution of synonymous, nonsynonymous and neutral polymorphisms across space.
a, b, Fraction of all genome-wide nonsynonymous a and synonymous b mutations present in the local genotype (n = 502 locations). c, Ratio of nonsynonymous to synonymous fractions (Kn/Ks). d–f, Spearman’s ρ correlation of Kn/Ks with degrees longitude (d), degrees latitude (e) and precipitation in July (f) (n = 502 for all comparisons). High selection intensity (Fig. 3c) coincided with locations where natural lines have a lower-than-average ratio of nonsynonymous to synonymous polymorphisms (Spearman’s ρ = −0.276, P = 3 × 10−10; a, b), high local genetic diversity π (Spearman’s ρ = 0.187, P = 2.63×10−5; a, b) and elevated Tajima’s D (Spearman’s ρ = 0.161, P = 3 × 10−4; d–f and Fig. 3e) (see Supplementary Table 11). Various demographic scenarios could partially explain some of these patterns in isolation: bottlenecks can reduce the nonsynonymous polymorphisms because they are typically at low frequency, or high diversity might be found in old, large populations. However, all patterns are in agreement with stronger natural selection having acted more efficiently on nonsynonymous mutations in southern latitudes. In addition, high diversity could be driven by strong natural selection fluctuating over time, with alternative polymorphisms having been selected depending on interannual precipitation cycles (Fig. 3f). All in all, we did not find evidence that the warm edge of the geographical distribution of A. thaliana is formed by an increase in drift, which would cause small populations to accumulate nonsynonymous deleterious mutations and become genetically depauperate. Rather, our observations and predictions indicate that the species’ warm geographical limit is primarily defined by the environmental tolerance limits, where climate-driven natural selection limits the survival of individuals and populations outside the species range and only a few, highly specialized genotypes can survive near the range edges.
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Exposito-Alonso, M., 500 Genomes Field Experiment Team., Burbano, H.A. et al. Natural selection on the Arabidopsis thaliana genome in present and future climates. Nature 573, 126–129 (2019). https://doi.org/10.1038/s41586-019-1520-9
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