Chemical and physical signals mediating conspecific and heterospecific aggregation behavior of first instar stink bugs.

We investigated cues that mediate the aggregation behavior of immature pentatomid bugs by using nymphs of six different pentatomid bug species (Nezara viridula, Acrosternum hilare, Chlorochroa ligata, Chlorochroa sayi, Thyanta pallidovirens, and Euschistus conspersus). When first instars of any two species were put together in a Petri dish, they readily formed heterospecific aggregations similar to their natural conspecific aggregations. The chemical profiles of first and second instar nymphs of each species were determined by solvent extraction with pentane, followed by GC-MS analysis. Immature bugs of the different species had some compounds in common, and some that were more species specific. Within a species, there were distinct differences in the profiles of compounds extracted from first and second instars. Bugs did not aggregate around untreated polysulfone beads (1 mm diam) that were glued together in groups approximating bug egg masses, suggesting that tactile cues alone were insufficient to induce aggregation. Furthermore, when tested over a range of doses, groups of polysulfone beads treated with crude whole-body extracts of bugs did not induce or maintain aggregations. However, first instar N. viridula nymphs did respond to beads treated with two of the three major components of bug extracts. 4-Oxo-(E)-2-decenal induced significant aggregations at two doses, whereas tridecane, the major component in extracts from all six species, did not, and (E)-2-decenal was repellent. The repellence of (E)-2-decenal may explain why we and previous researchers were unable to induce aggregations of first instar N. viridula using whole-body extracts.

Insect oviposition induces volatile emission in herbaceous plants that attracts egg parasitoids.

The egg parasitoid Trissolcus basalis (Wollaston) (Hymenoptera: Scelionidae) responded to synomones emitted by leguminous plants induced by feeding and oviposition activity of the bug Nezara viridula (L.) (Heteroptera: Pentatomidae). This was shown by laboratory bioassays using a Y-tube olfactometer. Broad bean leaves (Vicia faba L.) damaged by feeding activity of N. viridula and on which host egg mass had been laid produced synomones that attracted T. basalis. By contrast, undamaged leaves or feeding-damaged leaves without eggs did not attract wasp females. French bean plants (Phaseolus vulgaris L.) also emitted attractive synomones when they were damaged by host feeding and carrying egg masses. Thus, release of feeding- and oviposition-induced synomones does not seem to be plant-specific. Synomone production was shown to be a systemically induced plant physiological response to feeding damage and oviposition. Also, parts of the plant that were left undamaged and did not carry host eggs emitted attractive synomones when other parts of the plant were damaged by feeding and carrying eggs. Furthermore, wasps were not attracted by N. viridula egg masses offered alone or combined with damaged broad bean leaves. Thus, the attractiveness of feeding-damaged leaves carrying eggs is due to induction by feeding and oviposition rather than due to a combined effect of attractive volatiles released from eggs and damaged leaves. The production of synomones was influenced by the age of the host egg mass, because feeding-damaged leaves bearing egg masses attracted the parasitoid until the eggs were approximately 72-96 h old but not once the larvae had hatched from the eggs (approximately 120 h old). These results show that annual plants are able to produce synomones as a consequence of feeding and egg mass oviposition by a sucking insect.