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ABSTRACT Theory suggests that the drivers of demographic variation and local adaptation are shared and may feedback on one other. Despite some evidence for these links in controlled settings, the relationship between local adaptation and demography remains largely unexplored in natural conditions. Using 10 years of demographic data and two reciprocal transplant experiments, we tested predictions about the relationship between the magnitude of local adaptation and demographic variation (population growth rates and their elasticities to vital rates) across 10 populations of a well‐studied annual plant. In both years, we found a strong unimodal relationship between mean home‐away local adaptation and stochastic population growth rates. Other predicted links were either weakly or not supported by our data. Our results suggest that declining and rapidly growing populations exhibit reduced local adaptation, potentially due to maladaptation and relaxed selection, respectively. 

PremiseWhether drought‐adaptation mechanisms tend to evolve together, evolve independently, or evolve constrained by genetic architecture is incompletely resolved, particularly for water‐relations traits besides gas exchange. We addressed this issue in two subspecies ofClarkia xantiana(Onagraceae), California winter annuals that separated approximately 65,000 years ago and are adapted, partly by differences in flowering time, to native ranges differing in precipitation. MethodsIn these subspecies and in recombinant inbred lines (RILs) from a cross between them, we scored traits related to drought adaptation (timing of seed germination and of flowering, succulence, pressure–volume curve variables) in common environments. ResultsThe subspecies native to more arid environments (parviflora) exhibited slower seed germination in saturated conditions, earlier flowering, and greater succulence, likely indicating superior drought avoidance, drought escape, and dehydration resistance via water storage. The other subspecies (xantiana) had lower osmotic potential at full turgor and lower water potential at turgor loss, implying superior dehydration tolerance. Genetic correlations among RILs suggest facilitated evolution of some trait combinations and independence of others. Where genetic correlations exist, subspecies differences fell along them, with the exception of differences in succulence and turgor loss point. In that case, subspecies difference overcame genetic correlations, possibly reflecting strong selection and/or antagonistic genetic correlations with other traits. ConclusionsClarkia xantianasubspecies’ differ in multiple mechanisms of drought adaptation. Genetic architecture generally does not seem to have constrained the evolution of these mechanisms, and it may have facilitated the evolution of some of trait combinations.