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REARING DIAPAUSE AND DIAPAUSE-FREE WESTERN SPRUCE BUDWORM (CHORISTONEURA OCCIDENTALIS) (LEPIDOPTERA: TORTRICIDAE) ON AN ARTIFICIAL DIET

Published online by Cambridge University Press:  31 May 2012

R. L. Lyon
Affiliation:
Pacific Southwest Forest and Range Experiment Station, Forest Service, Berkeley, California
C. E. Richmond
Affiliation:
Pacific Southwest Forest and Range Experiment Station, Forest Service, Berkeley, California
J. L. Robertson
Affiliation:
Pacific Southwest Forest and Range Experiment Station, Forest Service, Berkeley, California
B. A. Lucas
Affiliation:
Pacific Southwest Forest and Range Experiment Station, Forest Service, Berkeley, California
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Abstract

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The western spruce budworm, Choiistoneura occidentalis Freeman, which normally passes through an obligate diapause in nature, was reared in the laboratory without diapause. The critical factor for preventing diapause appeared to be the physical environment presented to the first stage larvae. The response of C. occidentalis was flexible. The 2nd stage larvae could be made to diapause or forego diapause, depending on their rearing experience in the first stage. By eliminating diapause it was possible to rear about 7½ generations per year as against about 2¼ under normal diapause conditions. The diapause of the jack-pine budworm, C. pinus pinus Freeman, and C. lambertiana californica Powell, could be prevented by the same technique. The diapause of the spruce budworm, C. fumiferana (Clemens), could not be eliminated except after several generations of selection.

Type
Articles
Copyright
Copyright © Entomological Society of Canada 1972

References

Allen, D. C., Knight, F. B., and Foltz, J. L.. 1968. A technique for rearing Choristoneura pinus on artificial diet. Ann. ent. Soc. Am. 61: 362364.CrossRefGoogle Scholar
Bean, J. L. and Batzer, H. O.. 1957. Mean head width for spruce budworm larval instars in Minnesota and associated data. J. econ. Ent. 50: 499.CrossRefGoogle Scholar
Beck, S. D. 1968. Insect photoperiodism. Academic Press, New York. 288 p.Google Scholar
Freeman, T. N. 1967. On coniferophagous species of Choristoneura (Lepidoptera: Tortricidae) in North America. I. Some new forms of Choristoneura allied to C. fumiferana. Can. Ent. 99: 449455.CrossRefGoogle Scholar
Grisdale, D. 1970. An improved laboratory method for rearing large numbers of spruce budworm, Choristoneura fumiferana (Lepidoptera: Tortricidae). Can. Ent. 102: 11111117.CrossRefGoogle Scholar
Harvey, G. T. 1957. The occurrence and nature of diapause-free develovment in the spruce budworm, Choristoneura fumiferana (Clem.) (Lepidoptera: Tortricidae). Can. J. zool. 35: 549572.CrossRefGoogle Scholar
Harvey, G. T. 1958. A relationship between photoperiod and cold-storage treatment in the spruce budworm. Science 128: 12051206.CrossRefGoogle ScholarPubMed
McMorran, A. 1965. A synthetic diet for the spruce budworm, Choristoneura fumiferana (Clem.) (Lepidoptera: Tortricidae). Can. Ent. 97: 5862.CrossRefGoogle Scholar
Pitman, G. B. 1963. Some environmental factors influencing rearing of the spruce budworm, Choristoneura fumiferana (Clem.) (Lepidoptera: Tortricidae) under laboratory conditions. MS. Thesis, Oregon State University, Corvallis. 105 p.Google Scholar
Whiteside, J. M. and Carolin, V. M. Jr. 1961. Spruce budworm in the western United States. U.S. Dep. Agric. For. Pest Leafl. 53, 8 p.Google Scholar