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Intraspecific variation in morphology and behavior is widespread, especially in species with large distribution ranges. This includes foraging which can vary according to the local resource landscape. How this may be linked to differences in social structure, especially in socially foraging species is less known. Greater spear-nosed bats are well known for their large repertoire of often highly complex social behaviors. In Trinidad, they form stable groups of unrelated females that recruit other members to temporally unpredictable flowering balsa trees. We compared these findings with a dataset of capture data, GPS tracks, and observations collected over six years in a colony in Panamá. We found profound differences in the foraging behavior and group stability ofPhyllostomus hastatusduring the dry season where social behaviors were expected. Female bats did not coordinate commutes to exploit distinct foraging resources as a group. Instead, females commuted individually to very distant foraging areas which overlapped between groups. Linked to this we found groups to be unstable in size over the short and long term. Our findings highlight the large intraspecific variation and indicate a strong influence of the local resource landscape and associated benefits of social foraging on the social structure in these bats and possibly many other animals. 

All foraging animals face a trade-off: how much time should they invest in exploitation of known resources versus exploration to discover new resources? For group-living central place foragers, this balance is challenging. Due to the nature of their movement patterns, exploration and exploitation are often mutually exclusive, while the availability of social information may discourage individuals from exploring. To examine these trade-offs, we GPS-tracked groups of greater spear-nosed bats (Phyllostomus hastatus) from three colonies on Isla Colón, Panamá. During the dry season, when these omnivores forage on the nectar of unpredictable balsa flowers, bats consistently travelled long distances to remote, colony-specific foraging areas, bypassing flowering trees closer to their roosts. They continued using these areas in the wet season, when feeding on a diverse, presumably ubiquitous diet, but also visited other, similarly distant foraging areas. Foraging areas were shared within but not always between colonies. Our longitudinal dataset suggests that bats from each colony invest in long-distance commutes to socially learned shared foraging areas, bypassing other available food patches. Rather than exploring nearby resources, these bats exploit colony-specific foraging locations that appear to be culturally transmitted. These results give insight into how social animals might diverge from optimal foraging.