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DELAYED DEVELOPMENT OF MICROCTONUS VITTATAE (HYMENOPTERA: BRACONIDAE) IN SUPERPARASITIZED ADULTS OF PHYLLOTRETA CRUCIFERAE (COLEOPTERA: CHRYSOMELIDAE)

Published online by Cambridge University Press:  31 May 2012

H. G. Wylie
H. G. Wylie
Affiliation:
Research Station, Agriculture Canada, Winnipeg, Manitoba R3T 2M9
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Extract

The length of the developmental period from oviposition to adult emergence for nondiapausing individuals of a solitary endophagous braconid, Microctonus vittatae Mues., was usually about 4 wk at 20°C, 70–80% R.H., and a 16h:8h L:D cycle. However, living second and subsequent instar parasite larvae were occasionally found in adults of Phyllotreta cruciferae (Goeze) and Phyllotreta striolata (F.) (Coleoptera: Chrysomelidae) dissected 25–30 days after parasitization. Most of these beetles also contained one or more dead parasite eggs or first-instar larvae, suggesting that superparasitism prolonged development of the single surviving parasite in each host. Therefore, the effect of superparasitism on the parasite's development was investigated by recording the length of the developmental period of M. vittatae in two groups of adult P. cruciferae, one consisting of a majority of superparasitized individuals and the other mostly of hosts with only one immature parasite each.

Type
Articles
Information
The Canadian Entomologist , Volume 115 , Issue 4 , April 1983 , pp. 441 - 442
Copyright
Copyright © Entomological Society of Canada 1983

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References

Edson, K. M. and Vinson, S. B.. 1979. A comparative morphology of the venom apparatus of female braconids (Hymenoptera: Braconidae). Can. Ent. 111: 1013–1024.CrossRefGoogle Scholar
Gerling, D. 1972. The developmental biology of Telenomus remus Nixon (Hym., Scelionidae). Bull. ent. Res. 61: 385–388.CrossRefGoogle Scholar
Jackson, D. J. 1963. Diapause in Caraphractus cinctus Walker (Hymenoptera: Mymaridae), a parasitoid of the eggs of Dytiscidae (Coleoptera). Parasitology 53: 225–251.CrossRefGoogle Scholar
Olton, G. S. and Legner, E. F.. 1974. Biology of Tachinaephagus zealandicus (Hymenoptera: Encyrtidae), parasitoid of synanthropic Diptera. Can. Ent. 106: 785–800.CrossRefGoogle Scholar
Simmonds, F. J. 1943. The occurrence of superparasitism in Nemeritis canescens Grav. Rev. Can. Zool. 2: 15–58.Google Scholar
Vinson, S. B. and Iwantsch, G. F.. 1980. Host regulation by insect parasitoids. Q. Rev. Biol. 55: 143–165.CrossRefGoogle Scholar
Vinson, S. B. and Sroka, P.. 1978. Effects of superparasitism by a solitary endoparasitoid on the host, parasitoid, and field samplings. Southwest Ent. 3: 299–303.Google Scholar
Wylie, H. G. 1977. Observations on Athrycia cinerea (Diptera: Tachinidae), a parasite of Mamestra configurata (Lepidoptera: Noctuidae). Can. Ent. 109: 747–754.CrossRefGoogle Scholar
Ziser, S. W., Wojtowicz, J. A., and Nettles, W. C. Jr., 1977. The effects of the number of maggots per host on the length of development, puparial weight and adult emergence of Eucelatoria sp. Ann. ent. Soc. Am. 70: 733–736.CrossRefGoogle Scholar