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Abstract Island biotas provide unparalleled opportunities to examine evolutionary processes. Founder effects and bottlenecks, e.g., typically decrease genetic diversity in island populations, while selection for reduced dispersal can increase population structure. Given that support for these generalities mostly comes from single-species analyses, assemblage-level comparisons are needed to clarify how (i) colonization affects the gene pools of interacting insular organisms, and (ii) patterns of genetic differentiation vary within assemblages of organisms. Here, we use genome-wide sequence data from ultraconserved elements (UCEs) to compare the genetic diversity and population structure of mainland and island populations of nine ant species in coastal southern California. As expected, island populations (from Santa Cruz Island) had lower expected heterozygosity and Watterson’s theta compared to mainland populations (from the Lompoc Valley). Island populations, however, exhibited smaller genetic distances among samples, indicating less population subdivision. Within the focal assemblage, pairwise Fst values revealed pronounced interspecific variation in mainland-island differentiation, which increases with gyne body size. Our results reveal population differences across an assemblage of interacting species and illuminate general patterns of insularization in ants. Compared to single-species studies, our analysis of nine conspecific population pairs from the same island-mainland system offers a powerful approach to studying fundamental evolutionary processes. 

Non-native plant species can disrupt plant–pollinator interactions by altering pollinator foraging behavior, which can in turn affect levels of interspecific pollen transfer between native and nonnative plant species. These processes may be amplified in cases where introduced plant species act as magnet taxa that enhance pollinator visitation to other plant species. We investigated these interactions on Santa Cruz Island (Santa Barbara Co., California) between non-native fennel (Foeniculum vulgare), a widespread and abundant invader, and the endemic Santa Cruz Island buckwheat (Eriogonum arborescens), which broadly overlaps fennel in its local distribution and blooming phenology. A fennel flower removal experiment revealed that this invader acts as a magnet species by increasing insect visitation to adjacent buckwheat flowers. Analysis of the amount of pollen carried on the bodies of insect pollinators (i.e., pollen transport) revealed that 96% of visitors to buckwheat flowers carried fennel pollen and 72% of visitors to fennel flowers carried buckwheat pollen. Pollen transport analyses and visitation rate data further suggest that members of three bee genera (primarily Augochlorella) may be responsible for the majority of fennel pollen deposited on the stigmas of buckwheat flowers (i.e., pollen transfer) and vice versa. Lastly, fennel pollen transport appeared to occur at a larger spatial scale than the magnet effect that fennel plants exert on floral visitors to neighboring buckwheat plants. The ability of fennel to act as a magnet species, coupled with the fact that it is widespread invader with known allelopathic capacities, suggests that future studies could evaluate if the transfer of fennel pollen adversely affects native plant reproduction in areas where fennel is introduced.