DEVELOPMENT AND ENCAPSULATION OF THE ENDOPARASITOID, MICROPLITIS-CROCEIPES (HYM, BRACONIDAE), IN 6 CANDIDATE HOST SPECIES (LEP)

Citation
D. Blumberg et Sm. Ferkovich, DEVELOPMENT AND ENCAPSULATION OF THE ENDOPARASITOID, MICROPLITIS-CROCEIPES (HYM, BRACONIDAE), IN 6 CANDIDATE HOST SPECIES (LEP), Entomophaga, 39(3-4), 1994, pp. 293-302
Citations number
35
Categorie Soggetti
Entomology
Journal title
ISSN journal
00138959
Volume
39
Issue
3-4
Year of publication
1994
Pages
293 - 302
Database
ISI
SICI code
0013-8959(1994)39:3-4<293:DAEOTE>2.0.ZU;2-S
Abstract
Encapsulation and development of the endoparasitoid, Microplitis croce ipes (Cresson), were studied in six atypical lepidopteran host species whose usual host is Helicoverpa tea (Boddie). The candidate hosts exa mined were: the fall army worm Spodoptera frugiperda (J.E. Smith); the beet armyworm, Spodoptera exigua (Hubner); the cabbage looper, Tricho plusia ni (Hubner); the greater wax moth, Galleria mellonella (L.); th e Indian meal moth, Plodia interpunctella (Hubner); and the diamondbac k moth, Plutella xylostella (L.). Both S. exigua and T. ni were comple tely unsuitable for M. croceipes development due to the high rate of e ggs that were encapsulated within three days after parasitism. Encapsu lation in S. frugiperda included mainly parasitoid eggs and was first detected six days after parasitization at 25 degrees C and two days at 30 degrees C. Encapsulation in C. mellonella occurred only in the lar val stage of the parasitoid. In P. interpunctella, parasitoid, larvae reached the 3rd stadium, but none of them pupated. Only S. frugiperda and G. mellonella supported successful development of M. croceipes fro m egg to adult. The percentage of parasitoids reaching the adult stage in these hosts was higher at 30 degrees C than at 25 degrees C (13% v s. 4% in S. frugiperda, and 21% vs. 3% in G. mellonella, respectively) . However, these percentages were too low to substitute them as a more economical host for rearing M. croceipes. This biological information will be useful in additional laboratory studies directed toward reduc ing the rate of encapsulation (e.g., manipulation of host rearing temp erature) to increase production of M. croceipes on these hosts.