We studied the factors which regulate the reproduction of ectoparasites of temperate-zone cave-dwelling bats, using the Schreiber's bat (Miniopterus schreibersii) and its ectoparasites as a model. For this, we searched 969 bats during 2003 and 2004 at important stages of the bat yearly cycle and found four ectoparasite species regularly occurring on them: two nycteribiids (Nycteribia schmidlii and Penicillidia conspicua), one wing mite (Spinturnix psi), and one hard tick (Ixodes simplex simplex). These parasites were present throughout the yearly cycle, but their reproductive activity greatly fluctuated seasonally. Also, we found that sex, age, and reproductive status of the host strongly influenced the reproductive activity of parasites. Overall, the four parasite species had a similar reproductive pattern, reproducing more intensively during the pregnancy and nursing seasons of M. schreibersii, mainly on pregnant and juvenile bats. Moreover, parasites greatly reduced reproductive activity during winter, while bats were in deep torpor or hibernating. We conclude that reproduction in ectoparasites of M. schreibersii and of many other temperate cave-dwelling bats is mostly regulated by the reproductive cycle of their bat hosts, but also limited by roost temperatures during winter. The fact that the reproductive cycle of parasite species of such distinct taxonomic groups are similarly adjusted to that of their bat host suggests that this adjustment is a highly adaptive trait.
Ectoparasitism may be recognized as one of the main costs of coloniality, but little is known about how it affects the fitness and social structure of bats, the most gregarious of mammals. We studied these issues using the colonial bat Miniopterus schreibersii and its haematophagous parasitic mite Spinturnix psi as a model. Body condition is an important indicator of individual fitness that is potentially affected by ectoparasitism. Thus, we measured host body condition and mite loads in a total of 969 bats throughout the annual cycle. Mites were rare while hosts hibernated, increased in abundance in spring and peaked during nursing season of bats, when they were particularly abundant on lactating females and young bats. This strong seasonal variation in mite loads is related to the reproductive cycle of mites, which in turn appears to be synchronized with the reproductive cycle of their hosts. Mite loads and the condition of bats were negatively correlated, and information available suggests that this may be due to an effect of parasitism, although other possible causes for this trend cannot be excluded. However, a negative correlation was only observed during the bat's nursing season, when mites were most abundant, and heavily parasitized bats lost about 10% of their weight. Mite parasitism did not seem to be a significant disadvantage of coloniality, except in nurseries, where it might impose some costs. However, as females and young usually aggregate in these colonies, we presume that for them such costs are probably offset by advantages of group living. Adult males, however, are usually absent from nurseries, which may be a strategy to minimize mite parasitism. Overall, the results suggest that ectoparasitism may play a role in determining the social structure of M. schreibersii and of many other temperate bats that have similar life cycles and ectoparasitic loads.
Nycteribiids (Diptera: Nycteribiidae) are specific haematophagous ectoparasites of bats, which spend nearly all their adult lives on hosts. However, females have to leave bats to deposit their larva on the walls of the roosts, where they later emerge as adult flies. Nycteribiids had thus to evolve efficient sensorial mechanisms to locate hosts from a distance. We studied the sensory cues involved in this process, experimentally testing the role of specific host odours, and general cues such as carbon dioxide, body heat, and vibrations. As models we used two nycteribiids (Penicillidia conspicua and Penicillidia dufourii) and their primary bat hosts (Miniopterus schreibersii and Myotis myotis, respectively). Carbon dioxide was the most effective cue activating and orientating the responses of nycteribiids, followed by body heat and body odours. They also responded to vibration, but did not orientate to its source. In addition, sensory cues combined (carbon dioxide and body heat) were more effective in orientating nycteribiids than either cue delivered alone. Results suggest that nycteribids have some capacity to distinguish specific hosts from a distance, probably through their specific body odours. However, the strong reliance of nycteribiids on cues combined indicates that they follow these to orientate to nearby multispecies bat clusters, where the chances of finding their primary hosts are high. The combination of sensory cues seems therefore an effective strategy used by nycteribiids to locate bat hosts at a distance.
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