A mosaic of chemical coevolution in a large blue butterfly.

Mechanisms of recognition are essential to the evolution of mutualistic and parasitic interactions between species. One such example is the larval mimicry that Maculinea butterfly caterpillars use to parasitize Myrmica ant colonies. We found that the greater the match between the surface chemistry of Maculinea alcon and two of its host Myrmica species, the more easily ant colonies were exploited. The geographic patterns of surface chemistry indicate an ongoing coevolutionary arms race between the butterflies and Myrmica rubra, which has significant genetic differentiation between populations, but not between the butterflies and a second, sympatric host, Myrmica ruginodis, which has panmictic populations. Alternative hosts may therefore provide an evolutionary refuge for a parasite during periods of counteradaptation by their preferred hosts.

The propolis of stingless bees: terpenes from the tibia of three Frieseomelitta species.

The posterior tibia of foraging workers of three species of Frieseomelitta (Hymenoptera: Meliponinae) stingless bees have been shown to carry complex mixtures of plant-derived mono-, sesqui-, di- and tri-terpenes. These subtances were not found on the fore- or mid-legs, nor on other parts of the hind legs. F. silvestrii and F. silvestrii languida, when collecting, appear to exploit different plants for their resin even when housed in the same area. F. varia were found to be not collecting resin at the time of the initial sampling and were therefore sampled later. Mature foragers carry the resin. In the samples studied here, particularly prominent were the monoterpene alpha-pinene, the sesquiterpenes beta-caryophyllene, alpha-cubebene, alpha- and gamma-muurolene, gamma-cadinene, germacrene-D, and elemol and the diterpenes manool and totarol The collected material is used for the resin placed around the entrance to their nests and is also mixed with wax, to produce the cerum used for the structures in the nest.