Eucoilinae

Members of the genus Aganaspis are the only eucoilines thus far utilized in biological control efforts against Tephritidae (Clausen 1978; Wharton et al. 1998; Ovruski et al. 2000). Two species have been so utilized: A. daci and A. pelleranoi (Hayward, K. J. 1940, Baranowski et al. 1993).

Eucoilines have been reared from hosts representing a wide range of microhabitats, and several species have been reared from flies breeding in fruit. Relatively few of the eucoilines reared from fruit have been unequivocally associated with tephritid hosts. The most reliable host records from Tephritidae are for the genera Aganaspis and Odontosema. Four species of Aganaspis and one species of Odontosema have been repeatedly reared both from isolated puparia of tephritids and from samples that produced only tephritids and no other Diptera, thus confirming their status as hosts.

Additionally, there are published records for Dicerataspis and Lopheucoila that strongly suggest that members of these genera at least occasionally attack Tephritidae even though they normally attack hosts in other families. At least one species of Ealata has been also reared on several occasions from fruit infested with tephritids, but hosts are as yet unconfirmed. Finally, there are records of Rhoptomeris and Trybliographa attacking tephritids in the New World, but these are likely misidentifications of some of the more difficult and poorly defined New World genera of eucoilines. A revision of the New World genera will be necessary before these host relationships can be clarified. Wharton et al. (1998) provide a detailed summary of published records referring to species of Rhoptromeris and Trybliographa that have been associated with tephritids.

Many of the eucoilines reared from fruits are actually parasitoids of Drosophilidae, Lonchaeidae, Phoridae or other flies associated with ripe and decomposing fruit. Members of the genus Leptopilina, for example, are well-known as parasitoids of Drosophilidae and are among the mostly commonly encountered eucoilines reared from fruit samples in the Afrotropics. Though Drosophilidae tend to colonize fruit after tephritids have departed to pupate in the soil, there is potential for overlap. For example, fruits that have fallen from a tree may have more rapidly decaying portions inhabited by Drosophilidae at the same time as more sound portions still inhabited by tephritid larvae. Since fruit is often collected and reared in bulk, it is easy to obtain parasitoids of both Drosophilidae and Tephritidae from the same sample. Thus, in order to assess host specificity accurately, it is essential to verify all records by isolating individual puparia or exposing known hosts to ovipositing females. For many of the older records (including label data from unpublished studies), this was not done and host associations must therefore be viewed with caution. It is likely that the tephritid host records for Rhoptromeris haywardi (Blanchard) and Trybliographa brasiliensis (von Ihering) actually refer to drosophilids for these reasons. Puparia of most fruit-infesting tephritids do not have the posterior spiracles protruding from the surface and this will help in distinguishing them from many of the other Diptera noted here.

Since most fruit-infesting tephritids are considerably larger than fruit-infesting drosophilids, and their eucoiline parasitoids are solitary, it is therefore often possible to distinguish drosophilid parasitoids from tephritid parasitoids simply by differences in their size. Some tephritids are quite small, however, making such associations somewhat risky in the absence of isolated puparia.

Members of the subfamily Eucoilinae are solitary endoparasitoids that oviposit in the larval stage of cyclorrhaphous Diptera and emerge as adults from the host puparium.

The eucoiline Figitidae can be readily recognized by the presence of a raised plate on the dorsal surface of the scutellum (1, 2, 3). Additionally, males and females can nearly always be distinguished from one another by differences in the number of antennal segments. Males have 15 and females have 13. This is helpful because the genitalia (1, 2) are often concealed by the apical abdominal terga.

Eucoilines are worldwide in distribution, but with the exception of the widely introduced southeast Asian species Aganaspis daci Weld, most of the confirmed rearing records from Tephritidae are from the neotropics.

The standard work on classification and identification of eucoilines is Weld’s (1952) privately printed catalog of the Cynipoidea. Nordlander (1978, 1980, 1981, 1982) has updated major parts of this classification, Lin (1987) subsequently described the genus Aganaspis, and Quinlan (1986, 1988) treated Afrotropical genera. A phylogenetic analysis of eucolines has also been published (Fontal-Cazalla et al. 2002).

Numerous images are available at the MorphBank site, http://www.morphbank.net, relative to species and taxa discussed here and in the other eucoiline pages on the Paroffit site. See the following pages for additional information Aganaspis, Dicerataspis, Ealata, and Odontosema.

The eucoiline Figitidae are sometimes treated as a distinct family, the Eucoilidae. In some of the older literature, they are treated as a subfamily of Cynipidae rather than as a subfamily of Figitidae. For current classification, we follow Ronquist (1995).

Eucoilinae er en gruppe av stilkvepser. De er beslektet med gallvepser (Cynipidae) men i motsetning til disse er de parasitoider som snylter på andre insekter. Man kjenner nær 1000 arter, omtrent 220 er funnet i Europa og det er sannsynlig at vi har ca. 60 arter i Norge.