Competing hypotheses explaining species' use of resources have been advanced. Resource limitations in habitat and/or food are factors that affect assemblages of species. These limitations could drive the evolution of morphological and/or behavioural specialization, permitting the coexistence of closely related species through resource partitioning and niche differentiation. Alternatively, when resources are unlimited, fluctuations in resources availability will cause concomitant shifts in resource use regardless of species identity. Here, we used next-generation sequencing to test these hypotheses and characterize the diversity, overlap and seasonal variation in the diet of three species of insectivorous bats of the genus Pteronotus. We identified 465 prey (MOTUs) in the guano of 192 individuals. Lepidoptera and Diptera represented the most consumed insect orders. Diet of bats exhibited a moderate level of overlap, with the highest value between Pteronotus parnellii and Pteronotus personatus in the wet season. We found higher dietary overlap between species during the same seasons than within any single species across seasons. This suggests that diets of the three species are driven more by prey availability than by any particular predator-specific characteristic. P. davyi and P. personatus increased their dietary breadth during the dry season, whereas P. parnellii diet was broader and had the highest effective number of prey species in all seasons. This supports the existence of dietary flexibility in generalist bats and dietary niche overlapping among groups of closely related species in highly seasonal ecosystems. Moreover, the abundance and availability of insect prey may drive the diet of insectivores.

1. Interspecific competition (IC) is often seen as a main driver of evolutionary patterns and community structure. Bats might compete for key resources, and cases of exaggerated divergence of resource-related characters or trait overdispersion in bat assemblages are often explained in terms of current or past interspecific competition. However, other pressures leading to patterns that mimic the outcome of competition cannot always be ruled out. 2. We present the state of knowledge on IC among bats, providing a critical evaluation of the information available and identifying open questions and challenges. 3. We reviewed 100 documents addressing potential or actual IC in bats and categorised them in terms of the resource for which bats compete (food, foraging habitat, roosts, water, and acoustic space). We also examined the ecomorphological and behavioural traits considered therein to highlight responses to IC or niche partitioning. 4. We found that: although resources should be limiting in order for competition to occur, this is seldom tested; sympatry is sometimes taken as synonymous of syntopy (yet sympatric species that are not syntopic will never experience competition); comparisons between sympatry and allopatry are rare; and testing of objective criteria exploring the existence of niche partitioning or character displacement is not commonly adopted. 5. While morphological examination of food remains in droppings has often led to coarse-grained analysis that proved insufficient to establish the occurrence of food niche overlap or partitioning, new frontiers are being opened by state-of-the-art molecular dietary analysis. 6. A better understanding of IC in bats is paramount, since distributional changes leading to novel bat assemblages driven by climate change are already taking place, and the dramatic decline in insect availability, as well as the global loss or alteration of foraging habitat, may generate new competitive interactions or exacerbate existing interactions in the Anthropocene, and into the future.

Along with its many advantages, social roosting imposes a major risk of pathogen transmission. How social animals reduce this risk is poorly documented. We used lipopolysaccharide challenge to imitate bacterial infection in both a captive and a free-living colony of an extremely social, long-lived mammal-the Egyptian fruit bat. We monitored behavioral and physiological responses using an arsenal of methods, including onboard GPS to track foraging, acceleration sensors to monitor movement, infrared video to record social behavior, and blood samples to measure immune markers. Sick-like (immune-challenged) bats exhibited an increased immune response, as well as classic illness symptoms, including fever, weight loss, anorexia, and lethargy. Notably, the bats also exhibited behaviors that would reduce pathogen transfer. They perched alone and appeared to voluntarily isolate themselves from the group by leaving the social cluster, which is extremely atypical for this species. The sick-like individuals in the open colony ceased foraging outdoors for at least two nights, thus reducing transmission to neighboring colonies. Together, these sickness behaviors demonstrate a strong, integrative immune response that promotes recovery of infected individuals while reducing pathogen transmission inside and outside the roost, including spillover events to other species, such as humans.

Climate change is among the key anthropogenic factors affecting species’ distribution, with important consequences for conservation. However, little is known concerning the consequences of distributional changes on community‐level interactions, and responses by generalist species might have many ecological implications in terms of novel interactions with resident species. In this study, we applied Ecological Niche Models and niche analysis to three generalist bat species, Hypsugo savii, Pipistrellus kuhlii, and Pipistrellus pipistrellus, which share similar ecological traits and are sympatric in parts of their ranges. Our aims were to investigate how predicted climate change will affect species’ distribution and to analyse the degree of climatic niche overlap between the three species, in both the current and the future scenarios (2050 and 2070; Representative Concentration Pathways 4.5 and 8.5). Temperatures were the most important predictors influencing species’ range expansion in future. According to our models, Pipistrellus kuhlii and Hypsugo savii may expand their geographic ranges towards northern latitudes, whereas the geographic range of the less thermophilous Pipistrellus will shift northwards, resulting in it losing the southern portion in Europe. The already considerable degree of climatic niche overlap between the three species will increase further in future. On the basis of our findings, within the new areas potentially colonised by all three species in future, alterations in community‐level balance might occur, bringing about effects that are only partially predictable. In view of this, we highlight the need for further research and improved monitoring of bat communities in areas that are predicted to be particularly vulnerable to climate change.