Social insects employ a range of behaviours to protect their colonies against disease, but little is known about how such collective behaviours are orchestrated. This is especially true for the social Blattodea (termites). We developed an experimental approach that allowed us to explore how the social response to disease is co-ordinated by multistep host-pathogen interactions. We infected the eastern subterranean termite Reticulitermes flavipes with the entomopathogenic fungus Metarhizium anisopliae, and then, at different stages of infection, reintroduced them to healthy nestmates and recorded behavioural responses. As expected, termites groomed pathogen-exposed individuals significantly more than controls; however, grooming was significantly elevated after fungal germination than before, demonstrating the importance of fungal status to hygienic behaviour. Significantly, we found that cannibalism became prevalent only after exposed termites became visibly ill, highlighting the importance of host condition as a cue for social hygienic behaviour. Our study reveals the presence of a coordinated social response to disease that depends on stage of infection. Specifically, we show how the host may play a key role in triggering its own sacrifice. Sacrificial self-flagging has been observed in other social insects: our results demonstrate that termites have independently evolved to both recognize and destructively respond to sickness.

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.

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This is an author version of the contribution published on:Questa è la versione dell'autore dell'opera: Journal of Experimental Marine Biology and Ecology, 453, 2014, doi:10.1016/j.jembe.2014 The definitive version is available at: La versione definitiva è disponibile alla URL: ABSTRACTMating opportunities fluctuate in the wild and hermaphrodites have the chance of partitioning reproductive resources between their two sexual functions accordingly, i.e., they have a plastic sex allocation. Plasticity is usually promoted by environmental fluctuations butmay be affected by species-specific factors, which may be revealed by comparisons between related species.We testedwhether polychaeteworms of three related species of simultaneous hermaphrodites, Ophryotrocha diadema, Ophryotrocha adherens and Ophryotrocha gracilis, had plastic male and female allocation. We measured the costs of the female function and investigated whether the costs might affect the magnitude of plasticity in this function. To these aims, we exposed adult worms to three levels of mating opportunities and measured their female and male functions. In our experimental conditions, there was no adjustment in the male function, the cheapest function, whereas the three species differed in how they adjusted their allocation into the female function to mating opportunities. O. diadema and O. adherens worms exhibited highly plastic female allocation, and plasticitywas consistent across three measures of female function. In contrast, O. gracilis worms had a fixed female allocation, irrespective of mating opportunities. Additionally, when the sexual functions were relatively costly, their plasticity was greater than when they were relatively cheap. However, the magnitude of the plasticity did not depend solely on species-specific costs of the function, but also on the features of the mating system of each species.