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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.

Stereoisomers of 4-methyl-3-heptanol are major components of aggregation pheromones of bark beetles and trail pheromones of ants. Recently, (3S,4S)-4-methyl-3-heptanol (I) has been tentatively identified as the main component of the aggregation pheromone of the almond bark beetle, Scolytus amygdali (Coleoptera: Scolytidae). The four stereoisomers of 4-methyl-3-heptanol were prepared and bioassayed. Key steps included preparation of chiral 4-methyl-3-heptanones using SAMP and RAMP reagents, reduction to the corresponding alcohols, and stereospecific transesterification with vinyl acetate with lipase AK catalysis. In field tests, only (3S,4S)-4-methyl-3-heptanol attracted beetles in combination with the synergist (3S,4S)-4-methyl-3-hexanol, whereas (3R,4S)- and (3R,4R)-4-methyl-3-heptanols were inhibitory.

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