To understand the factors governing the diversity, abundance and host associations of parasitoids attacking frugivorous drosophilid flies on Iriomote-jima, a subtropical island of Japan, we monitored parasitism on several occasions over the period 2003–2009. Fifteen drosophilid and 12 parasitoid species were recorded. Three species of Drosophila, D. bipectinata, D. albomicans and D. takahashii, bred abundantly in banana baits, though their abundance varied between years and seasons. Frequent parasitoid species were Asobara japonica, A. pleuralis (Braconidae), Leptopilina ryukyuensis and L. pacifica (Figitidae). L. victoriae was recorded only in December 2003. In addition, host acceptance and host suitability of the four most frequently recorded parasitoid species were studied in the laboratory. Most parasitoid and drosophilid species showed species-specific associations with more than one antagonist species, suggesting that they have been subjected to complex coevolutionary interactions. In addition, host range of most of the parasitoid species included one of the three major Drosophila species, suggesting that the abundance of potential hosts is one of the factors determining the evolution of parasitoid host use., Biljan Novkovic ... [et al.]., and Obsahuje seznam literatury
In central Japan Ganaspis xanthopoda and Asobara japonica commonly parasitize the larvae of frugivorous drosophilids, mainly in montane forests, and urban environments and small groves, respectively. These two parasitoids start reproduction about one month later than their host drosophilids, probably to avoid searching for hosts when host density is low in early spring. It is likely that the local variation in the abundance of these parasitoids and a temporal refuge for their hosts contribute to the persistence of this parasitoid-host community. The forest species, G. xanthopoda, parasitized at least three Drosophila species that are abundant in forests, supporting the hypothesis that parasitoids are better adapted to attack frequently-encountered host species. This parasitoid did not parasitize drosophilid species that are phylogenetically distantly-related to the three host species or less frequent in forests. Benefits of using such species as host would not exceed the costs of evolving virulence to them. Another parasitoid, A. japonica, parasitized various indigenous and exotic drosophilid species including those that it rarely encountered in the field. It is not clear why this species has such a wide host range.
We studied variations in genetic, physiological, and ecological traits, and the phylogenetic relationship among sexual and parthenogenetic populations of Asobara japonica, a larval parasitoid of drosophilid flies, in order to understand how they adapt to local environments and have differentiated. The strain from Iriomote-jima (IR) differed from other Japanese strains in the nucleotide sequences of its cytochrome oxidase subunit I (COI) and in not undergoing diapause and having a shorter preimaginal period and a higher adult tolerance of cold. The strains other than IR showed a low level of nucleotide variation in COI but varied in their mode of reproduction; the strains from the Ryukyu Islands were sexual, whereas those from the main islands of Japan and Ogasawara were parthenogenetic. In addition, strains from higher latitudes generally showed a high incidence of diapause, although there were some exceptions. On the other hand, preimaginal period and adult cold tolerance varied little among the strains excluding IR, and pupal cold tolerance, oviposition preference and incidence of parasitism varied little among the strains including IR. Evolution and environmental adaptations in this species are discussed, particularly focusing on parthenogenetic populations.