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Abstract In cleptoparasitic bees, host aggression and detection avoidance might be the main selective pressures shaping host-parasite interactions. However, the behavioral responses toward parasitism are unknown for most host species. In this study, we investigated the host-parasite interactions and behaviors of the cleptoparasitic beeTriepeolus remigatuswhen parasitizing the nests of its host, the squash beeXenoglossa(Peponapis)pruinosa. Using circle-tube behavioral assays and direct observations at a nest aggregation ofX. pruinosa, we assessed whether interactions between host and parasite were aggressive, tolerant, or avoidant and characterized the general parasitic behavior ofT. remigatus. Our results reveal a lack of aggression between host and cuckoo bees, with interactions primarily characterized by tolerant and avoidant behaviors. Squash bees displayed minimal aggression toward both conspecifics and parasites. Interestingly, despite the absence of aggressive responses,T. remigatuspreferred entering nests while the host was foraging, potentially indicating a strategy to avoid the discovery of parasitic visits. Furthermore, field observations provided insights into the parasitic behavior ofT. remigatus, revealing primarily rapid visits to host nests without extensive inspection. The limited aggression and short time for nest visits observed inT. remigatussuggest adaptations to optimize parasitic success while minimizing host detection. Overall, our findings contribute to a better understanding of the behavior of open-cell parasites and provide a first accounting of the squash bee behavior when encountering parasitic bees. Further research is needed to elucidate the mechanisms underlying host-parasite coevolution and response to parasitism in ground-nesting bees. 

The expansion of agriculture is responsible for the mass conversion of biologically diverse natural environments into managed agroecosystems dominated by a handful of genetically homogeneous crop species. Agricultural ecosystems typically have very different abiotic and ecological conditions from those they replaced and create potential niches for those species that are able to exploit the abundant resources offered by crop plants. While there are well-studied examples of crop pests that have adapted into novel agricultural niches, the impact of agricultural intensification on the evolution of crop mutualists such as pollinators is poorly understood. We combined genealogical inference from genomic data with archaeological records to demonstrate that the Holocene demographic history of a wild specialist pollinator of Cucurbita (pumpkins, squashes, and gourds) has been profoundly impacted by the history of agricultural expansion in North America. Populations of the squash bee Eucera pruinosa experienced rapid growth in areas where agriculture intensified within the past 1,000 y, suggesting that the cultivation of Cucurbita in North America has increased the amount of floral resources available to these bees. In addition, we found that roughly 20% of this bee species’ genome shows signatures of recent selective sweeps. These signatures are overwhelmingly concentrated in populations from eastern North America where squash bees were historically able to colonize novel environments due to human cultivation of Cucurbita pepo and now exclusively inhabit agricultural niches. These results suggest that the widespread cultivation of crops can prompt adaptation in wild pollinators through the distinct ecological conditions imposed by agricultural environments.