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RELATION OF SEXUPARA PRODUCTION IN THE WOOLLY PEAR APHID, ERIOSOMA PYRICOLA (HOMOPTERA: PEMPHIGIDAE), TO TREE GROWTH IN THE FIELD

Published online by Cambridge University Press:  31 May 2012

K. G. Swenson
Affiliation:
Entomology Department, Oregon State University, Cornallis

Abstract

Sexupara production in the pear root aphid, Eriosoma pyricola Baker & Davidson, was closely associated with the cessation of shoot growth of its host in the field in irrigated and non-irrigated plots in two successive, but phenologically different years. Neither the environment nor the host plant were unfavorable at the time the sexuparae were formed, indicating that the aphid uses the host plant as a source of seasonal information.

The nature of synchronization between active development of univoltine insects and trees is discussed. It is concluded that the initiation of dormancy in trees and diapause in insects is not likely to be synchronized by a common set of environmental factors. Either regulation of insect diapause by host trees is more common than is currently recognized, or environmental and age differences in tree growth have favored selection for obligate diapause.

Type
Articles
Copyright
Copyright © Entomological Society of Canada 1971

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References

Baker, A. C., and Davidson, W. M.. 1916. Woolly pear aphis. J. agric. Res. 6: 351360.Google Scholar
Ball, E. D. 1920. The life cycle in Hemiptera. Ann. ent. Soc. Am. 13: 142151.CrossRefGoogle Scholar
Buckle, W. 1963. Morphendifferenzierung der Chaetophoriden des Ahorns in Abhangigkeit von Klimafaktoren und Physiologie der Wirtsflanze. Zool. Jahrb. Anat. 80: 385458.Google Scholar
Danilevskii, A. S. 1965. Photoperiodism and seasonal development of insects. Oliver and Boyd, Edinburgh. 283 pp. (English ed.)Google Scholar
Feeny, P. P. 1968. Effect of oak leaf tannins on larval growth of the winter moth Operophthera brumata. J. Insect Physiol. 14: 801817.CrossRefGoogle Scholar
Hartzell, A. 1937. Bionomics of the plum and peach leafhopper, Macropsis trimaculata. Contr. Boyce Thompson Inst. Pl. Res. 9: 121136.Google Scholar
Hille Ris Lambers, D. 1966. Notes on California aphids, with descriptions of new genera and new species (Homoptera: Aphididae). Hilgardia 37: 569623.CrossRefGoogle Scholar
Judge, F. D. 1968. Polymorphism in a subterranean aphid, Pemphigus bursarius I. Factors affecting the development of sexuparae. Ann. ent. Soc. Am. 61: 819827.CrossRefGoogle Scholar
Kramer, P. J. 1943. Amount and duration of growth of various species of tree seedlings. Plant Physiol. 18: 239251.CrossRefGoogle ScholarPubMed
Lees, A. D. 1966. The control of polymorphism in aphids. Adv. Insect Physiol. 3: 207277.CrossRefGoogle Scholar
Lees, A. D. 1968. Photoperiodism in insects. Photophysiology 4: 47137.CrossRefGoogle Scholar
Nienstaedt, H. 1966. Dormancy and dormancy release in white spruce. Forest Sci. 12: 374384.Google Scholar
Rombergr, J. A. 1963. Meristems, growth, and development in woody plants. U.S. Dep. Agric. Tech. Bull. 1293, 214 pp.Google Scholar
Sethi, S. L., and Swenson, K. G.. 1967. Formation of sexuparae in the aphid, Eriosoma pyricola, on pear roots. Ent. exp. appl. 10: 97102.CrossRefGoogle Scholar
Vegis, A. 1964. Dormancy in higher plants. A. Rev. Pl. Physiol. 15: 185224.CrossRefGoogle Scholar