Abstract

Ptilinus fuscus (Anobiidae) was confirmed as the host species of Pelecotoma fennica (Rhipiphoridae, Pelecotominae). Females of Pelecotoma oviposit into the wood infested by the host larvae. First-instar larvae are elongate, unsclerotized, very different from the triungulinid larvae known in other rhipiphorids. They search actively for the host larvae in the wood; no phoresy is involved in the life cycle. The first-instar larvae temporarily paralyse the host larva and enter its body, overwintering (some perhaps more than once) as an endoparasite. In the spring of the year of emergence, the endoparasite engorges enormously (without moulting) and develops a special sclerotized caudal structure which is then used for perforation of the host's integument. The larva undergoes a further four ectoparasitic instars. The fifth (i.e. fourth ectoparasitic) instar differs considerably from the preceding three, and is capable of boring through the wood to prepare the emergence gallery for the adult. Pupation occurs in the wood. The rate of parasitization may locally far exceed 50%. Superparasitization by the first-instar larvae is possible, but usually only 1 larva survives to the ectoparasitic stage. Larval morphology of Pelecotoma is described and illustrated. Additional data on bionomics and larval morphology are also presented for the genus Metoecus (Rhipiphorinae). Comparing the biology and larval morphology of Pelecotoma with other Rhipiphoridae, it is assumed that ancestral rhipiphorids may have been xylophilous Tenebrionoidea with predaceous or omnivorous larvae, and that the ‘triungulinid’ larvae and phoretic habits may not belong to the groundplan of the family Rhipiphoridae. The widespread opinion considering Rhipiphoridae closely related to the family Mordellidae is questioned.

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