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Honeybee disappearance is one of the major environmental and economic challenges this century has to face. The ecto-parasitic mite Varroa destructor represents one of the main causes of the worldwide beehive losses. Although halting mite transmission among beehives is of primary importance to save honeybee colonies from further decline, the natural route used by mites to abandon a collapsing colony has not been extensively investigated so far. Here, we explored whether, with increasing mite abundance within the colony, mites change their behaviour to maximize the chances of leaving a highly infested colony. We show that, at low mite abundance, mites remain within the colony and promote their reproduction by riding nurses that they distinguish from foragers by different chemical cuticular signatures. When mite abundance increases, the chemical profile of nurses and foragers tends to overlap, promoting mite departure from exploited colonies by riding pollen foragers., (© 2014. Published by The Company of Biologists Ltd.)

Insect social life is governed by chemicals. A great number of studies have demonstrated that the blend of hydrocarbons present on the cuticle (CHCs) plays a pivotal role in intra- and inter-specific communication. It is not surprising, therefore, that social parasites, specialized in exploiting the costly parental care provided by host workers, exploit the host chemical communication system too. Throughout their life cycle, social parasites intercept and break this CHC-based code. Recently, however, several polar compounds (mainly peptides) have been found in addition to CHCs both on the cuticle and on the comb surface of social insects, and their semiochemical role has been demonstrated in some circumstances. In the present study, we used the paper wasp social parasite-host system Polistes sulcifer (Zimmerman)-Polistes dominulus (Christ) to evaluate the relative importance of the CHCs and polar compounds in two different steps of the host exploitation process: host nest detection by the pre-usurping parasite and parasite chemical integration into the host colony. After separating the polar and apolar fractions of the host nest as well as those of pre- and post-usurpation parasites, we carried out laboratory assays based on the binary choice model. Our results show that nest polar compounds neither are used by the parasite to detect the host's nest nor play a role in parasite chemical integration into the host colony. In contrast, we demonstrate that CHCs are fundamental in both steps, thus confirming their primary role in social insect life and consequently in social parasite-host interactions.

Social life offers animals increased fitness opportunities. However, the advantages are not evenly distributed and some individuals benefit more than others. The ultimate advantage of reaching the highest rank in a dominance hierarchy is the achievement of reproduction monopoly. In social insects, dominant individuals and queens keep their reproductive control through differential oophagy of unwanted eggs (egg policing). Egg recognition is the main proximate mechanism for maintaining reproductive dominance. In the social wasp Polistes dominulus, subordinate queens often lay eggs in the presence of the dominant individual. Combining gas chromatography-mass spectrometry (GC-MS) analysis and laboratory bioassays, we found that chemical differences between eggs of subordinate and dominant foundresses can explain the differential success in oophagy enjoyed by dominant individuals. We propose that dominance behaviour is an investigative behaviour as well as a ritualized agonistic behaviour. In fact, the frequency of dominance acts increases with the chemical similarity of the surfaces of dominant- and subordinate-laid eggs. Therefore, dominant individuals probably perform dominance behaviour to test the cuticular signatures of subordinates and so better assess the chemical profiles of subordinate eggs. Finally, we provide evidence that in particular social contexts, subordinate Polistes foundresses can develop ovaries as large as those of dominant individuals but nevertheless lay very few eggs. The subordinates probably lay a limited number of eggs to avoid unnecessary energy loss, as a result of efficient queen policing, but will start laying eggs as soon as the queen fails.

Foundresses and workers of Polistes paper wasps show slight morphological and physiological differences. However, after the emergence of the workers, the castes can be readily discriminated by their behaviour: the dominant foundress is the principal egg-layer, whereas workers perform different tasks linked to colony development. Previous studies have demonstrated in this genus that defence of the colony by the workers is more effectively carried out by a collective response elicited by venom volatiles used as alarm pheromones. In the present study, gas chromatography-mass spectrometry analyses of the venom volatiles of foundresses and workers of Polistes dominulus (Christ) show predominantly quantitative differences. Spiroacetals, mainly (E,E)-2,8-dimethyl-1,7-dioxaspiro[5.5]undecane, are significantly higher in the venom volatiles fraction of workers, whereas the amount of N-(3-methylbutyl)acetamide is almost double in foundresses. On the basis of the chemical results, behavioural assays were performed on fifteen field colonies to test the alarm response of the resident wasps to venom extracts from foundresses and workers. Our behavioural results suggest that worker venom has a stronger alarm effect on the colonies than that of the foundresses, which seems unable to elicit the complete alarm response ending with a final attack and sting. The venom volatiles of P. dominulus workers serve mainly to alarm the colony whilst those of foundresses may also be linked to additional functions related to conspecific interactions.