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The robber fly Mallophora ruficauda Weidemann (Diptera: Asilidae) is an important pest of apiculture in the Pampas of Argentina. As adults, they prey on honey bees and other insects, whereas the larvae are ectoparasitoids of Scarabaeidae grubs. Females of M. ruficauda lay eggs in grassland where the larvae drop to the ground after being wind‐dispersed and burrow underground searching for their hosts. A temporal asynchrony exists between the appearance of the parasitoid larvae and the host, with the parasitoid appearing earlier than the host. The present study investigates whether a strategy of synchronization with the host exists in M. ruficauda and determines which of the larval instars are responsible for it. Survival patterns and duration of the immature stages of the parasitoid are investigated to determine whether there is a modulation in the development at any time that could reduce the asynchrony. Experiments are carried out to determine the survival and duration of free‐living larval stadia in the absence of cues associated with the host. It is established that the first instar is capable of moulting to the second instar without feeding and in the absence of any cues related to the host, a unique event for parasitoids. Also, the first instar of M. ruficauda moults to the second stage within a narrow temporal window, and the second instar never moults in the absence of the host. After parasitizing a host, the second instar has the longest lifespan and is the most variable with respect to survival compared with the rest of the instars. All larval instars, except for those in the last (fifth) stadium, have a similar rate of mortality to that of second‐instar larvae. Additionally, it is established that the host is killed during the fourth (parasitoid) stadium and that the first‐ and fifth‐larval instars develop independently of the host. Finally, possible mechanisms that could aid in compensating for the asynchrony between the parasitoid and the host, promoting the host–parasitoid encounter, are discussed.

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Lice from pinnipeds – sea lions, seals and walruses – are the only insects capable of surviving marine dives. Throughout their evolutionary history, they have adapted to tolerate hypoxia, high salinity, low temperature and, in particular, to tolerate conditions of high hydrostatic pressure. To understand the limits of the capacity of lice to survive during host deep dives, we conducted a series of controlled experiments in the laboratory. We collected lice from elephant seals and submitted the different life stages to high pressure conditions. Lice were first exposed to one of four hydrostatic pressures: 30, 80, 150 or 200 kg cm−2. They were then exposed a second time to higher or lower hydrostatic pressure conditions to test for the impact of the first experience, which could either be deleterious or trigger physiological adaption, allowing them a better tolerance to high pressure. We found that lice from elephant seals can tolerate hydrostatic pressures higher than 200 kg cm−2 (close to 200 atm), which is equivalent to 2000 m depth. Adults exhibited lower recovery times than nymphs after immersion at high hydrostatic pressure. Our findings show that lice have developed unique adaptations to endure extreme marine conditions. We discuss these extreme performances in relation to the morphological characteristics and physiological responses to diving in these insects.

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