Climate and the biotic community structure plant resistance across biogeographic groups of yellow monkeyflower.

Characterizing correlates of phytochemical resistance trait variation across a landscape can provide insight into the ecological factors that have shaped the evolution of resistance arsenals. Using field-collected data and a greenhouse common garden experiment, we assessed the relative influences of abiotic and biotic drivers of genetic-based defense trait variation across 41 yellow monkeyflower populations from western and eastern North America and the United Kingdom. Populations experience different climates, herbivore communities, and neighboring vegetative communities, and have distinct phytochemical resistance arsenals. Similarities in climate as well as herbivore and vegetative communities decline with increasing physical distance separating populations, and phytochemical resistance arsenal composition shows a similarly decreasing trend. Of the abiotic and biotic factors examined, temperature and the neighboring vegetation community had the strongest relative effects on resistance arsenal differentiation, whereas herbivore community composition and precipitation have relatively small effects. Rather than simply controlling for geographic proximity, we jointly assessed the relative strengths of both geographic and ecological variables on phytochemical arsenal compositional dissimilarity. Overall, our results illustrate how abiotic conditions and biotic interactions shape plant defense traits in natural populations.

Population genomic and historical analysis suggests a global invasion by bridgehead processes in Mimulus guttatus.

Imperfect historical records and complex demographic histories present challenges for reconstructing the history of biological invasions. Here, we combine historical records, extensive worldwide and genome-wide sampling, and demographic analyses to investigate the global invasion of Mimulus guttatus from North America to Europe and the Southwest Pacific. By sampling 521 plants from 158 native and introduced populations genotyped at >44,000 loci, we determined that invasive M. guttatus was first likely introduced to the British Isles from the Aleutian Islands (Alaska), followed by admixture from multiple parts of the native range. We hypothesise that populations in the British Isles then served as a bridgehead for vanguard invasions worldwide. Our results emphasise the highly admixed nature of introduced M. guttatus and demonstrate the potential of introduced populations to serve as sources of secondary admixture, producing novel hybrids. Unravelling the history of biological invasions provides a starting point to understand how invasive populations adapt to novel environments.