Overlap of Ecological Niche Breadth of Euglossa cordata and Eulaema nigrita (Hymenoptera, Apidae, Euglossini) Accessed by Pollen Loads and Species Distribution Modeling.

Urban areas can serve as biodiversity refuges for pollinators because of the high diversity of available floral and nesting resources. However, it remains unclear what plant species commonly used for urban landscaping provide floral resources that pollinators actively use. Here, we integrate data from the pollen and species distribution models of two abundant euglossine bees-the large-bodied Eulaema nigrita (Lepeletier, 1841) and the small-bodied Euglossa cordata (Linnaeus, 1758)-in urban areas to investigate their overlap in diet breadth and distribution. We hypothesized that because bees with larger body sizes tend to have larger foraging areas, large-bodied bees would have a wider diet breath than small-bodied bees. Contrary to our hypothesis, we found that Eg. cordata has a wider diet breadth than El. nigrita with the former species showing higher diversity of pollen types collected (per pollen load and on average across pollen loads). Pollen grains from Solanum paniculatum and Tradescantia zebrina represented 63% of the diet of Eg. cordata, whereas pollen from S. paniculatum and Psidium guajava represented 87% of the diet of El. nigrita. After overlaying the distribution of both bee species and the three most important pollen resources, the distribution models revealed that these three plant species can co-occur with both euglossine bees throughout a large portion of eastern Brazil near the coast. Thus, we conclude S. paniculatum, T. zebrina, and P. guajava should be considered key plants for the maintenance of these two urban euglossine bee species. The results of this study provide important information for urban landscaping programs that aim to protect and preserve pollinators.

Conservation of Queen Pheromones Across Two Species of Vespine Wasps.

Social insects are known for their reproductive division of labor between queens and workers, whereby queens lay the majority of the colony's eggs, and workers engage mostly in non-reproductive tasks. Queens produce pheromones that signal their presence and fertility to workers, which in turn generally remain sterile. Recently, it has been discovered that specific queen-characteristic cuticular hydrocarbons (CHCs) function as queen pheromones across multiple lineages of social insects. In the common wasp, Vespula vulgaris, several long-chain linear alkanes and 3-methylalkanes were shown to act as queen signals. Here, we describe similar bioassays with a related species of highly eusocial vespine wasp, the Saxon wasp, Dolichovespula saxonica. We show that a blend of queen-characteristic hydrocarbons that are structurally related to those of the common wasp inhibit worker reproduction, suggesting conservation of queen pheromones across social wasps. Overall, our results highlight the central importance of CHCs in chemical communication among social insects in general, and as conserved queen pheromones in these social wasps in particular.

Dual effect of wasp queen pheromone in regulating insect sociality.

Eusocial insects exhibit a remarkable reproductive division of labor between queens and largely sterile workers [1, 2]. Recently, it was shown that queens of diverse groups of social insects employ specific, evolutionarily conserved cuticular hydrocarbons to signal their presence and inhibit worker reproduction [3]. Workers also recognize and discriminate between eggs laid by the queen and those laid by workers, with the latter being destroyed by workers in a process known as "policing" [4, 5]. Worker policing represents a classic example of a conflict-reducing mechanism, in which the reproductive monopoly of the queen is maintained through the selective destruction of worker-laid eggs [5, 6]. However, the exact signals used in worker policing have thus far remained elusive [5, 7]. Here, we show that in the common wasp, Vespula vulgaris, the pheromone that signals egg maternity and enables the workers to selectively destroy worker-laid eggs is in fact the same as one of the sterility-inducing queen signals that we identified earlier [3]. These results imply that queen pheromones regulate insect sociality in two distinct and complementary ways, i.e., by signaling the queen's presence and inhibiting worker reproduction, and by facilitating the recognition and policing of worker-laid eggs.

The origin and evolution of social insect queen pheromones: Novel hypotheses and outstanding problems.

Queen pheromones, which signal the presence of a fertile queen and induce daughter workers to remain sterile, are considered to play a key role in regulating the reproductive division of labor of insect societies. Although queen pheromones were long thought to be highly taxon-specific, recent studies have shown that structurally related long-chain hydrocarbons act as conserved queen signals across several independently evolved lineages of social insects. These results imply that social insect queen pheromones are very ancient and likely derived from an ancestral signalling system that was already present in their common solitary ancestors. Based on these new insights, we here review the literature and speculate on what signal precursors social insect queen pheromones may have evolved from. Furthermore, we provide compelling evidence that these pheromones should best be seen as honest signals of fertility as opposed to suppressive agents that chemically sterilize the workers against their own best interests.

Conserved class of queen pheromones stops social insect workers from reproducing.

A major evolutionary transition to eusociality with reproductive division of labor between queens and workers has arisen independently at least 10 times in the ants, bees, and wasps. Pheromones produced by queens are thought to play a key role in regulating this complex social system, but their evolutionary history remains unknown. Here, we identify the first sterility-inducing queen pheromones in a wasp, bumblebee, and desert ant and synthesize existing data on compounds that characterize female fecundity in 64 species of social insects. Our results show that queen pheromones are strikingly conserved across at least three independent origins of eusociality, with wasps, ants, and some bees all appearing to use nonvolatile, saturated hydrocarbons to advertise fecundity and/or suppress worker reproduction. These results suggest that queen pheromones evolved from conserved signals of solitary ancestors.