Hostname: page-component-586b7cd67f-2brh9 Total loading time: 0 Render date: 2024-11-30T11:33:25.676Z Has data issue: false hasContentIssue false

Inheritance of seasonal cycles in Chrysoperla (Insecta: Neuroptera)

Published online by Cambridge University Press:  14 April 2009

Catherine A. Tauber
Affiliation:
Department of Entomology, Comstock Hall, Cornell University, Ithaca, N.Y. 14853, USA
Maurice J. Tauber
Affiliation:
Department of Entomology, Comstock Hall, Cornell University, Ithaca, N.Y. 14853, USA
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.

Two separate, but interacting, genetic systems underlie the variation in seasonal cycles among members of the Chrysoperla carnea species-complex. The two systems are expressed as all-or-none reproductive responses to photoperiod and prey (i.e. short-day/long-day requirement for reproduction versus long-day reproduction and prey requirement for reproduction versus reproduction without prey). In each case the alternative to reproduction is reproductive diapause. The photoperiodic responses are determined by alleles at two unlinked autosomal loci. The expression of dominance by the alleles at these loci varies among geographical populations. The genes that determine the photoperiodic responses also act as suppressors of the genes that govern responsiveness to prey. An autosomal, polygenic system, with a threshold for the expression of diapause, determines responsiveness to prey. The two genetic systems are important to seasonal diversification and speciation within the C. carnea species-complex.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1987

References

Arnold, S. J. (1981). The microevolution of feeding behavior. In Foraging Behavior (ed. Kamil, A. C. and Sargent, T. D.). New York: Garland STMP Press.Google Scholar
Endler, J. A. (1977). Geographic Variation, Speciation, and Clines. Princeton, NJ: Princeton University Press.Google ScholarPubMed
Falconer, D. S. (1981). Introduction to Quantitative Genetics, 2nd edn.London: Longman.Google Scholar
Ford, E. B. (1975). Ecological Genetics. London: Chapman and Hall.Google Scholar
Henry, C. S. (1982). Reply to Tauber and Tauber's ‘Sympatric speciation in Chrysopa: further discussion’. Annals of the Entomological Society of America 75, 34.CrossRefGoogle Scholar
Henry, C. S. (1983). Acoustic recognition of sibling species within the holarctic lacewing Chrysoperla carnea (Neuroptera: Chrysopidae). Systematic Entomology 8, 293301.CrossRefGoogle Scholar
Henry, C. S. (1985). Sibling species, call differences, and speciation in green lacewings (Neuroptera: Chrysopidae: Chrysoperla). Evolution 39, 965984.Google ScholarPubMed
Kondrashov, A. S. & Mina, M. V. (1986). Sympatric speciation: when is it possible? Biological Journal of the Linnean Society 27, 201223.CrossRefGoogle Scholar
Lewontin, R. C. (1986). How important is genetics for an understanding of evolution? American Zoologist 26, 811820.CrossRefGoogle Scholar
Manning, A. & Hirsch, J. (1971). The effects of artificial selection for slow mating in Drosophila simulans. II. Genetic analysis of the slow mating line. Animal Behaviour 19, 448453.CrossRefGoogle ScholarPubMed
Rohlf, F. J. & Sokal, R. R. (1981). Statistical Tables. New York: W.H. Freeman.Google Scholar
Sokal, R. R. & Rohlf, F. J. (1981). Biometry, 2nd edn.New York: W. H. Freeman.Google Scholar
Tauber, M. J. & Tauber, C. A. (1972). Geographic variation in critical photoperiod and in diapause intensity of Chrysopa carnea (Neuroptera). Journal of Insect Physiology 18, 2529.CrossRefGoogle Scholar
Tauber, M. J. & Tauber, C. A. (1973). Nutritional and photoperiodic control of the seasonal reproductive cycle in Chrysopa mohave. Journal of Insect Physiology 19, 729736.Google Scholar
Tauber, M. J. & Tauber, C. A. (1976 a). Developmental requirements of the univoltine Chrysopa downesi: photoperiodic stimuli and sensitive stages. Journal of Insect Physiology 22, 331335.CrossRefGoogle Scholar
Tauber, M. J. & Tauber, C. A. (1976 b). Environmental control of univoltinism and its evolution in an insect species. Canadian Journal of Zoology 54, 260266.CrossRefGoogle Scholar
Tauber, C. A. & Tauber, M. J. (1977). A genetic model for sympatric speciation through habitat diversification and seasonal isolation. Nature 268, 702705.CrossRefGoogle ScholarPubMed
Tauber, M. J. & Tauber, C. A. (1981). Seasonal responses and their geographic variation in Chrysopa downesi: ecophysiological and evolutionary considerations. Canadian Journal of Zoology 59, 370376.CrossRefGoogle Scholar
Tauber, C. A. & Tauber, M. J. (1982 a). Evolution of seasonal adaptations and life history traits in Chrysopa: response to diverse selective pressures. In Evolution and Genetics of Life Histories (ed. Dingle, H. & Hegmann, J. P.). New York: Springer-Verlag.Google Scholar
Tauber, C. A. & Tauber, M. J. (1982 b). Sympatric speciation in Chrysopa: further discussion. Annals of the Entomological Society of America 75, 12.CrossRefGoogle Scholar
Tauber, C. A. & Tauber, M. J. (1982 c). Maynard Smith's model and corroborating evidence: no reason for misinterpretation. Annals of the Entomological Society of America 75, 56.Google Scholar
Tauber, C. A. & Tauber, M. J. (1986 a). Ecophysiological responses in life-history evolution: evidence for their importance in a geographically widespread insect speciescomplex. Canadian Journal of Zoology 64, 875884.CrossRefGoogle Scholar
Tauber, C. A. & Tauber, M. J. (1986 b). Genetic variation in all-or-none life-history traits of the lacewing Chrysoperla carnea. Canadian Journal of Zoology 64, 15421544.CrossRefGoogle Scholar
Tauber, M. J., Tauber, C. A. & Masaki, S. (1986). Seasonal Adaptations of Insects. New York: Oxford University Press.Google Scholar
Tauber, C. A., Tauber, M. J. & Nechols, J. R. (1977). Two genes control seasonal isolation in sibling species. Science 197, 592593.CrossRefGoogle ScholarPubMed