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The reproductve biology of Varroa jacobsoni, whose females infest honeybee brood, was studied in natural and transparent artificial brood cells. These investigations were made under the headings of maturation behaviour and fertilization, and the influence of infestation rate of brood cells on the number of mated females produced per infesting Varroa.
Mating of Varroa daughters, observed in the transparent brood cells with time‐lapse video, occurs just after ecdysis and as soon as they arrive on the faecal accumulation prepared by the mother. Such females are remated for as long as no other freshly moulted daughter arrives on the faecal accumulation.
The number of spermatozoa stocked in the spermatheca increases with remating, a strong indication for sperm mixing in this species when brood cells contain more than one Varroa foundress.
The number of daughters per infesting mother decreases at higher rates of infestation per cell, but the proportion of such daughters with a mate rises sharply due to the higher probability of finding a male within multi‐infested cells. The number of mated daughters per mother is maximal in cells with two foundress Varroa females.
The frequency distributions of infesting mites in drone cells are aggregated, and approximate to negative binomial distributions.
We postulate from the above that the observed non‐random infestation by Varroa in drone brood augments the mite's mean reproductive success through the production of a higher number of mated daughters than the corresponding Poisson distributions would.
SUMMARY
Hard ticks spend most of their life isolated from passing vertebrates but require a blood meal to proceed to the next life stage (larva, nymph or adult). These opportunist ectoparasites must be capable of anticipating signals that render suitable hosts apparent. Large ungulates that tolerate a high ectoparasite burden are the favoured hosts of adult hard ticks. Ruminants, comprising the majority of ungulate species, must regularly eruct gases from the foregut to relieve excess pressure and maintain a chemical equilibrium. Through eructations from individuals, and particularly herds,ruminants inadvertently signal their presence to hard ticks. Here, we report that all adult hard tick species we tested are attracted to cud and demonstrate that these acarines possess olfactory receptor cells for the carboxylic acid, phenol and indole end-products of the rumen bioreactor. Compounds from each of these classes of volatiles attract ticks on their own,and mixtures of these volatiles based on rumen composition also attract. Appetence for rumen metabolites represents a fundamental resource-tracking adaptation by hard ticks for large roaming mammals.
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