Exotic species often cause severe alterations in native communities due to their ability to rapidly and efficiently utilize a broad spectrum of resources. In flower–visitor interactions, the breadth of resource use by native and exotic animals as well as the partitioning of resources among them is often estimated based on the number of (shared) plant species used as resources. However, whether a flower visitor is able to exploit plant resources has been shown to be delimited by functional floral traits such as morphological barriers or attractive or repellent chemical cues. Each of the ecologically relevant traits can be viewed as a dimension of a Hutchinsonian n‐dimensional hypervolume, which characterizes the range of phenotypes exploitable by a species. In this study, we quantified the sizes and overlaps of n‐dimensional hypervolumes defined by floral traits that are exploited by native and exotic flower visitors (afterwards referred to as exploited space, ES). In the heavily invaded Hawaii Volcanoes National Park, USA, we phenotyped 40 native and exotic plant species and recorded flower–visitor interactions. To quantify the size and overlap of ES, we applied dynamic range boxes. On average, exotic flower visitors were more generalized in resource use (larger ES) than natives ones, which is additionally indicated by the absence of native flower visitors on exotic flowering plant species. In particular, ES based on floral scent emission was larger for exotic flower visitors compared to native ones. The unevenly expanded ES of native and exotic animals led to an asymmetric overlap of floral ES where exotic flower visitors shared only a small proportion of their ES with natives but occupied a large proportion of the ES of natives. The asymmetry in resource use of native and exotic flower visitors suggests a potential advantage in resource exploitation of the latter, potentially explaining their success in Hawaiian ecosystems. Predicted range expansion of exotic plant and animal species may further increase the competition for and reduce the availability of resources for native animals. This may lead to further declines of native species and increasing threats for Hawaiian ecosystems. A http://onlinelibrary.wiley.com/doi/10.1111/1365-2435.12932/suppinfo is available for this article.

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Insects associate with a diversity of microbes that can shape host ecology and diversity by providing essential biological and adaptive services. For most insect groups, the evolutionary implications of host–microbe interactions remain poorly understood. Geographically discrete areas with high biodiversity offer powerful, simplified model systems to better understand insect–microbe interactions. Hawaii boasts a diverse endemic insect fauna (~6000 species) characterized by spectacular adaptive radiations. Despite this, little is known about the role of bacteria in shaping this diversity. To address this knowledge gap, we inaugurate the Native Hawaiian Insect Microbiome Initiative (NHIMI). The NHIMI is an effort intended to develop a framework for informing evolutionary and biological studies in Hawaii. To initiate this effort, we have sequenced the bacterial microbiomes of thirteen species representing iconic, endemic Hawaiian insect groups. Our results show that native Hawaiian insects associate with a diversity of bacteria that exhibit a wide phylogenetic breadth. Several groups show predictable associations with obligate microbes that permit diet specialization. Others exhibit unique ecological transitions that are correlated with shifts in their microbiomes (e.g., transition to carrion feeding from plant-feeding in Nysius wekiuicola). Finally, some groups, such as the Hawaiian Drosophila, have relatively diverse microbiomes with a conserved core of bacterial taxa across multiple species and islands.

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Seed-feeding Nysius insects (Hemiptera: Lygaeidae) have a symbiotic association with distinct intracellular bacteria, “Candidatus Schneideria nysicola” (Gammaproteobacteria). While many other hemipteran insect groups generally rely on bacterial symbionts that synthesize all ten essential amino acids lacking in their plant sap diets, the nutritional role of Schneideria in Nysius hosts that specialize on a more nutritionally complete seed-based diet has remained unknown. To determine the nutritional and functional capabilities of Schneideria, we sequenced the complete Schneideria genomes from three distantly related endemic Hawaiian Nysius seed bug species. The complete Schneideria genomes are highly conserved and perfectly syntenic among Hawaiian Nysius host species. Each circular chromosome is ∼0.57 megabases in size and encodes 537 protein-coding genes. They further exhibit a strong A + T nucleotide substitution bias with an average G + C nucleotide content of 29%. The predicted nutritional contribution of Schneideria includes four B-vitamins and five of the ten essential amino acids that likely match its hosts’ seed-based diet. Disrupted and degraded genes in Schneideria suggests that Hawaiian lineages are undergoing continued gene losses observed in the smaller genomes of the other more ancient hemipteran symbionts.