Macroevolution of perfume signalling in orchid bees.

Theory predicts that both stabilising selection and diversifying selection jointly contribute to the evolution of sexual signalling traits by (1) maintaining the integrity of communication signals within species and (2) promoting the diversification of traits among lineages. However, for many important signalling traits, little is known about whether these dynamics translate into predictable macroevolutionary signatures. Here, we test for macroevolutionary patterns consistent with sexual signalling theory in the perfume signals of neotropical orchid bees, a group well studied for their chemical sexual communication. Our results revealed both high species-specificity and elevated rates of evolution in perfume signals compared to nonsignalling traits. Perfume complexity was correlated with the number of congeners in a species' range, suggesting that perfume evolution may be tied to the remarkably high number of orchid bee species coexisting together in some neotropical communities. Finally, sister-pair comparisons were consistent with both rapid divergence at speciation and character displacement upon secondary contact. Together, our results provide new insight into the macroevolution of sexual signalling in insects.

Olfactory specialization for perfume collection in male orchid bees.

Insects rely on the olfactory system to detect a vast diversity of airborne molecules in their environment. Highly sensitive olfactory tuning is expected to evolve when detection of a particular chemical with great precision is required in the context of foraging and/or finding mates. Male neotropical orchid bees (Euglossini) collect odoriferous substances from multiple sources, store them in specialized tibial pouches and later expose them at display sites, presumably as mating signals to females. Previous analysis of tibial compounds among sympatric species revealed substantial chemical disparity in chemical composition among lineages with outstanding divergence between closely related species. Here, we tested whether specific perfume phenotypes coevolve with matching olfactory adaptations in male orchid bees to facilitate the location and harvest of species-specific perfume compounds. We conducted electroantennographic (EAG) measurements on males of 15 sympatric species in the genus Euglossa that were stimulated with 18 compounds present in variable proportions in male hind tibiae. Antennal response profiles were species-specific across all 15 species, but there was no conspicuous differentiation between closely related species. Instead, we found that the observed variation in EAG activity follows a Brownian motion model of trait evolution, where the probability of differentiation increases proportionally with lineage divergence time. However, we identified strong antennal responses for some chemicals that are present as major compounds in the perfume of the same species, thus suggesting that sensory specialization has occurred within multiple lineages. This sensory specialization was particularly apparent for semi-volatile molecules ('base note' compounds), thus supporting the idea that such compounds play an important role in chemical signaling of euglossine bees. Overall, our study found no close correspondence between antennal responses and behavioral preferences/tibial contents, but confirms the utility of EAG profiling for discovering certain behaviorally active compounds.

Enantioselective preference and high antennal sensitivity for (-)-Ipsdienol in scent-collecting male orchid bees, Euglossa cyanura.

Male neotropical orchid bees (Euglossini) collect volatile chemicals from their environment, store them in tibial pouches, and later expose their "perfumes" during a courtship display. Here, we showed that enantiomeric selectivity plays an important role in the choice of volatiles by male Euglossa cyanura in southern Mexico, and that behavioral selectivity is linked to antennal sensitivity. In field bioassays with equal concentrations of (+)-ipsdienol, (-)-ipsdienol, and racemate, males preferred the (-)-isomer to the racemate, while neglecting the (+)-isomer. Correspondingly, antennae of male E. cyanura showed larger electroantennographic responses to the (-)-isomer than to the (+)-isomer. In comparison, antennae of male Euglossa mixta, which are not attracted to any form of ipsdienol, showed lower electroantennographic responses to (-)-ipsdienol than did antennae of E. cyanura, and also did not differ in sensitivity with respect to the (+)- or (-)-isomers. We suggest that (-)-ipsdienol is an important component of perfume signals in male E. cyanura, which have undergone selection in favor of increased antennal sensitivity to that enantiomer.