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Mating and Oviposition of the Pale Western Cutworm, Agrotis orthogonia Morrison (Lepidoptera: Noctuidae), in the Laboratory1

Published online by Cambridge University Press:  31 May 2012

L. A. Jacobson
Affiliation:
Canada Agriculture Research Station, Lethbridge, Alberta

Abstract

In the laboratory 90.7% of both sexes of moths of the pale western cutworm, Agrotis orthogonia Morrison, emerged from pupae between noon and midnight; almost half emerged between 2 and 4 p.m. Mating, evidenced by spermatophores in the bursa copulatrix, occurred almost always at night, within 3 days of emergence, and at temperatures between 5 and 35 °C. Most females mated only once. Multiple matings, with a maximum of 3 times, occurred in less than 20% of females. Males mated with a maximum of three females. Eggs developed during the pupal stage and were ready for fertilization when the moths emerged. Oviposition began on the first or second day after mating, peaked soon after, and continued until just prior to death of females. Maximum oviposition by one female was 564 eggs, with means from 90 to 342. Oviposition occurred at all temperatures from 5 to 35 °C. with an optimum between 10 and 25 °C. More eggs were laid in the dark or in subdued light than in continuous bright light. Females when unfed could oviposit but when fed water or sugar solutions they laid more eggs. Longevity varied directly with feeding and inversely with temperature. Mean longevity of moths fed honey solution in the laboratory was 12 days for both sexes. A diurnal rhythm of oviposition occurred with distinct peaks; 80% or more of the eggs were laid between noon and early evening. Rhythm of oviposition was apparently initiated by light and could be reversed by reciprocal light regimens but was maintained in continuous dark or light. The maximum distance flown on a flight mill was 14.7 miles for males and 3.5 miles for females. Speed varied from less than 1 to almost 3 m.p.h.

Type
Articles
Copyright
Copyright © Entomological Society of Canada 1965

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References

Bruce, V. G., and Pittendrigh, C. S.. 1957. Endogenous rhythms in insects and microorganisms. Amer. Nat. 91: 179195.CrossRefGoogle Scholar
Callahan, P. S. 1958. Behavior of the imago of the corn earworm, Heliothis zea (Boddie), with special reference to emergence and reproduction. Ann. ent. Soc. Amer. 51: 271283.CrossRefGoogle Scholar
Cook, W. C. 1930. Field studies of the pale western cutworm, Porosagrotis orthogonia Morr. Montana Agric. Exp. Sta. Bull. 225.Google Scholar
Guppy, J. C. 1961. Life history and behavior of the armyworm, Pseudaletia unipuncta (Haw.) (Lepidoptera: Noctuidae), in eastern Ontario. Canad. Ent. 93: 11411153.CrossRefGoogle Scholar
Harker, J. E. 1961. Diurnal Rhythms, pp. 131146. In Steinhaus, E. A. and Smith, Ray F. (ed.). Annual Review of Entomology. Annual Reviews Inc., Palo Alto, California.Google Scholar
Jacobson, L. A. 1962. Diapause in eggs of the pale western cutworm, Agrotis orthogonia Morr. (Lepidoptera: Noctuidae). Canad. Ent. 94: 515522.CrossRefGoogle Scholar
Jacobson, L. A., and Blakely, P. E.. 1957. A method of rearing the pale western cutworm, Agrotis orthogonia Morr. (Lepidoptera: Phalaenidae), in the laboratory. Canad. Ent. 89: 8789.CrossRefGoogle Scholar
Jacobson, L. A., and Blakeley, P. E.. 1958a. Influence of temperature and moisture on hatching of eggs of the pale western cutworm, Agrotis orthogonia Morr. (Lepidoptera: Noctuidae). Canad. J. Plant Sci. 38: 127134.CrossRefGoogle Scholar
Jacobson, L. A., and Blakeley, P. E.. 1958b. Development, mortality from starvation, and oviposition of the pale western cutworm, Agrotis orthogonia Morr. (Lepidoptera: Noctuidae), when fed on various food plants. Canad. Ent. 90: 650653.CrossRefGoogle Scholar
Jacobson, L. A., and Blakeley, P. E.. 1959. Development and behavior of the army cutworm in the laboratory. Ann. ent. Soc. Amer. 52: 100105.CrossRefGoogle Scholar
Jacobson, L. A., and Blakeley, P. E.. 1960. Survival, development, and fecundity of the pale western cutworm, Agrotis orthogonia Morr. (Lepidoptera: Noctuidae), after starvation. Canad. Ent. 92: 184188.CrossRefGoogle Scholar
Koerwitz, F. L., and Pruess, K. P.. 1964. Migratory potential of the army cutworm. J. Kansas ent. Soc. 37: 234239.Google Scholar
Lukefahr, M. 1957. Mating and oviposition habits of the pink bollworm moth. J. econ. Ent. 50: 487490.CrossRefGoogle Scholar
Lukefahr, M. J., and Martin, D. F.. 1964. The effects of various larval and adult diets on the fecundity and longevity of the bollworm, tobacco budworm, and cotton leafworm. J. econ. Ent. 57: 233235.CrossRefGoogle Scholar
Ouye, M. T. et al. , 1964. Mating studies of the pink bollworm. J. econ. Ent. 57: 222225.CrossRefGoogle Scholar
Parker, J. R., Strand, A. L. and Seamans, H. L.. 1921. Pale western cutworm (Porosagrotis orthogonia Morr.). J. agric. Res. 22: 189321.Google Scholar
Pruess, K. P. 1963. Effects of food, temperature, and oviposition site on longevity and fecundity of the army cutworm. J. econ. Ent. 56: 219221.CrossRefGoogle Scholar