The occurrence of a kairomonal response of the parasitoid Anagyrus spec. nov. near pseudococci (Hymenoptera: Encyrtidae) to (+)‐(1R,3R)‐cis‐2,2‐dimethyl‐3‐isopropenyl‐cyclobutanemethanol acetate (PcA, namely, planococcyl acetate) and (S)‐(+)‐lavandulyl senecioate (LS), the respective female sex pheromones of its hosts, the citrus mealybug, Planococcus citri (Risso) and the vine mealybug, Planococcus ficus (Signoret) (Homoptera: Pseudococcidae) was investigated. Attraction to the pheromones was tested by employing pheromone traps in field trials and by static air olfactometer bioassays in the laboratory. Female wasps showed a significant response to LS, in both field and olfactometer experiments. No significant response was registered to the sex pheromone of P. citri. Despite the similarity between the structures of LS and its analogue (S)‐(+)‐lavandulyl isovalerate (LI), no significant response to the latter compound was observed. It seems that differences between the structures of the carboxylate moiety of the respective molecules (LS and LI) markedly affect the kairomonal attractiveness to the parasitoid. The kairomonal response of Anagyrus spec. nov. near pseudococci was neither influenced by the host habitat nor by the host species on which it developed. This suggested innate behaviour of Anagyrus spec. nov. near pseudococci, possibly derived from evolutionary relationships between the parasitoid and P. ficus. The practical implications of the results are discussed.
The physiological age of adult males of seven mealybug species was measured in relation to the elongation of the male pair of the waxy caudal filaments. These filaments begin to emerge after eclosion and reached their maximum length from 29.4-46.6 h. The studied males were divided into three age groups, expressed as percentages of the total waxy caudal filaments length. Attraction to a sex pheromone source was significantly higher in the oldest male group (maximum filaments growth) compared with youngest one. Only the oldest male group copulated successfully; few of the younger males tested displayed 'courtship' behavior towards conspecific virgin females. The calculated duration of the sexually active phase of the adult male life cycle varied among species ranging from 34.4 to 46.6 h. There were marked variations in the strength of attraction to a pheromone source according to time of day. There was a continuous decrease in sexual activity from morning to evening. Our findings reveal clear maturation periods for adult males of the seven studied species. The long immature phase of the adult male mealybug is probably also related to several physiological processes that are needed to complete male maturation. The most noticeable change is the elongation of the waxy caudal filaments. However, mating may be performed at any time ambient conditions are suitable. Whereas male mealybug flight towards a pheromone source is restricted to a few hours, the male may continue mating activity throughout its sexually active period.
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