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PREVENTING AND TERMINATING PUPAL DIAPAUSE IN ATHRYCIA CINEREA (DIPTERA: TACHINIDAE)1

Published online by Cambridge University Press:  31 May 2012

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

Abstract

Pupal diapause in Athrycia cinerea (Coq.), a larval parasite of bertha armyworm, Mamestra configurata Walk., was usually prevented if the parasite larvae were reared at 25°C, but not if they were reared at 20°C. Mature larvae of the parasite were more sensitive than younger larvae to this temperature effect. Diapause incidence in A. cinerea at 20°C was not reduced by using only young parent females for oviposition; by rearing the parent females at a high temperature (25°C) and long day (16 h) prior to and during oviposition; by using host larvae that had been light-programmed for non-diapause; or by increasing the photoperiod, to which the parasite larvae were exposed, from 12 to 16 h. Termination of pupal diapause was accelerated by low temperature; at least 24 weeks at 2 °C were required to synchronize adult emergence.

Type
Articles
Copyright
Copyright © Entomological Society of Canada 1977

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References

Anderson, J. F. and Kaya, H. K.. 1974. Diapause induction by photoperiod and temperature in the elm spanworm egg parasitoid, Ooencyrtus sp. Ann. ent. Soc. Am. 67: 845849.CrossRefGoogle Scholar
Benson, J. F. 1973. Intraspecific competition in the population dynamics of Bracon hebetor Say (Hymenoptera: Braconidae). J. Anim. Ecol. 42: 105124.CrossRefGoogle Scholar
Bucher, G. E. and Bracken, G. K.. 1976. The bertha armyworm, Mamestra configurata (Lepidoptera: Noctuidae). Artificial diet and rearing technique. Can. Ent. 108: 13271338.CrossRefGoogle Scholar
Danilevskii, A. S. 1965. Photoperiodism and seasonal development of insects. Oliver and Boyd, Edinburgh and London.Google Scholar
Horn, D. J. 1971. The relationship between a parasite, Tetrastichus incertus (Hymenoptera: Eulophidae), and its host, the alfalfa weevil, Hypera postica (Coleoptera: Curculionidae), in New York. Can. Ent. 103: 8394.CrossRefGoogle Scholar
Lees, A. D. 1955. The physiology of diapause in arthropods. Cambridge University Press.Google Scholar
Lees, A. D. 1956. The physiology and biochemistry of diapause. A. Rev. Ent. 1: 116.CrossRefGoogle Scholar
Maslennikova, V. A. 1958. (On the conditions determining the diapause in the parasitic Hymenoptera Apanteles glomeratus L. (Braconidae) and Pteromalus puparum L. (Chalcididae).) (In Russian; English summary.) Rev. Ent. U.R.S.S. 37: 538545.Google Scholar
Messenger, P. S. and Force, D. C.. 1963. An experimental host-parasite system: Therioaphis maculata (Buckton) — Praon palitans Muesebeck (Homoptera: Aphidiidae — Hymenoptera: Ecology 44: 532540.CrossRefGoogle Scholar
Saunders, D. S. 1965. Larval diapause of maternal origin: induction of diapause in Nasonia vitripennis (Walk.) (Hymenoptera: Pteromalidae). J. exp. Biol. 42: 495508.CrossRefGoogle Scholar
Saunders, D. S. 1975. Manipulation of the length of the sensitive period, and the induction of pupal diapause in the flesh fly, Sarcophaga argyrostoma. J. Ent. (A) 50: 107118.Google Scholar
Shon, F. L. and Shea, P. J.. 1976. Increased rearing efficiency of two hymenopterous parasites using a non-diapausing host species, Choristoneura occidentalis. Environ. Ent. 5: 277278.CrossRefGoogle Scholar
Simmonds, F. J. 1946. A factor affecting diapause in hymenopterous parasites. Bull. ent. Res. 37: 9597.CrossRefGoogle Scholar
Wylie, H. G. 1966. Some mechanisms that affect the sex ratio of Nasonia vitripennis (Walk.) (Hymenoptera: Pteromalidae) reared from superparasitized housefly pupae. Can. Ent. 98: 645653.Google Scholar