Hostname: page-component-78c5997874-j824f Total loading time: 0 Render date: 2024-11-08T08:14:51.899Z Has data issue: false hasContentIssue false
  • English
  • Français

Diapause in the gypsy moth: environment-specific mode of inheritance

Published online by Cambridge University Press:  14 April 2009

Carol Becker Lynch  and
Marjorie A. Hoy
Carol Becker Lynch
Affiliation:
Department of Biology, Wesleyan University, Middletown, Connecticut, 06457, U.S.A.
Marjorie A. Hoy
Affiliation:
U.S. Forest Service, Northeastern Forest Experiment Station, Hamden, Connecticut, 06514, U.S.A.
Rights & Permissions [Opens in a new window]

Summary

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Preliminary investigation of the genetic basis of diapause in the gypsy moth, Lymantria dispar, involved a comparison of reciprocal crosses between wild-type moths and a selectively bred ‘non-diapause’ strain with the parental stocks, where half of the eggs resulting from each of the four mating types were exposed to one month of chill at 5 °C. The presence of chill dramatically altered the phenotypic expression of diapause-dependent characteristics. Early hatching was completely recessive in unchilled eggs, while hatching time was intermediate in chilled eggs, and there was no difference between reciprocal hybrids. Proportion of eggs hatching and, therefore, number of larvae produced was also influenced by chill. Unchilled hybrids did not differ substantially from wild-type eggs, while chilled hybrids were closer to the performance of the selected line. In this case, a significant reciprocal difference indicated some involvement of sex-linkage in the inheritance of diapause.

Type
Research Article
Information
Genetics Research , Volume 32 , Issue 2 , October 1978 , pp. 129 - 133
Copyright
Copyright © Cambridge University Press 1978

References

REFERENCES

Goldschmidt, R. (1932). Untersuchungen zur Genetik der geographischen Variation. V. Analyse der Überwinterungskeit als Anpassungscharakter. Archiv für Entvncklungsmechanik der Organismen 126, 674–768.CrossRefGoogle Scholar
Goldschmidt, R. (1933). Untersuchungen zur Genetik der geographischen Variation. VII. Archiv für Entwicklungsmechanik der Organismen 130, 562–615.CrossRefGoogle Scholar
Harvey, W. R. (1960). Least squares analysis of data with unequal subclass numbers. Publication no. ARS-20–8, U.S. Department of Agriculture, Washington, D.C.Google Scholar
Hoy, M. A. (1977). Rapid response to selection for a nondiapausing gypsy moth. Science 196, 1462–1463.CrossRefGoogle ScholarPubMed
Kulman, H. M. (1971). Effects of insect defoliation on growth and mortality of trees. Annual Review of Entomology 16, 289–324.CrossRefGoogle Scholar
Masaki, S. (1956). The effect of temperature on the termination of diapause in the egg of Lymantria dispar Linné (Lepidoptera: Lymantriidae). Japanese Journal of Applied Zoology 21, 148–157.Google Scholar
Robinson, R. (1971). Lepidoptera Genetics. New York: Pergamon Press.CrossRefGoogle Scholar
Tazima, Y. (1964). The Genetics of the Silkworm. London: Logos Press.Google Scholar