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FACTORS AFFECTING EGG MATURATION AND OVIPOSITION BY AUTOGENOUS AEDES ATROPALPUS (DIPTERA: CULICIDAE)

Published online by Cambridge University Press:  31 May 2012

Anne Hudson
Affiliation:
Entomology Research Institute, Canada Department of Agriculture, Ottawa

Abstract

Autogenous Aedes atropalpus (Coquillet) females derived from larvae fed on a standard maximum diet, matured about the same numbers of eggs when supplied with water only or with 25% sucrose. Those maintained on water laid 56% of the number matured within 5 days of emergence, but the sugar-fed insects laid only 28% in the same time, and even after 35 days many were found to have retained their eggs. The physiological mechanism causing the delay was not associated with crop distention, nor with the nutritional changes brought about by ingested sugar.Nulliparous females mostly refused blood during the first ovarian cycle although a few did rake a blood meal. At the time of feeding the eggs were already mature and neither the protein nor carbohydrate of the host blood were utilized during the first ovarian cycle. Parous females fed on blood and used the protein for egg development and there was a rapid rise in haemolymph carbohydrate after feeding, indicating that the host blood sugars also were used immediately.Nullipars derived from larvae maintained on a very low diet did not seek a blood meal either, and in these only some eggs commenced development to various stages. Sugar feeding by these adults assisted both maturation and oviposition.

Type
Articles
Copyright
Copyright © Entomological Society of Canada 1970

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References

Bates, M. 1941. Studies in the technique of raising anopheline larvae. Am. J. trop. Med. 21: 103122.CrossRefGoogle Scholar
Christophers, S. R. 1911. The development of the egg follicle in Anophelines. Paludism 2: 7388.Google Scholar
Clements, A. N. 1956. Hormonal control of ovary development in mosquitoes. J. exp. Biol. 23: 211223.CrossRefGoogle Scholar
Corbet, P. S. 1967. Facultative autogeny in arctic mosquitoes. Nature 215: 662663.CrossRefGoogle Scholar
De Meillon, B., Sebastian, A., and Khan, Z. H.. 1967. Cane-sugar feeding in Culex pipiens fatigans. Bull. Wld Hlth Org. 36: 5365.Google ScholarPubMed
Dethier, V. G., and Bodenstein, D.. 1958. Hunger in the blowfly. Z. Tierpsychol. 15: 129140.CrossRefGoogle Scholar
Dethier, V. G., and Gelperin, A.. 1967. Hyperphagia in the blowfly. J. exp. Biol. 47: 191200.CrossRefGoogle Scholar
Detinova, T. S. 1945. On the influence of the glands of internal secretion upon the ripening of the gonads and the imaginal diapause in Anopheles maculipennis. Zool. Zh. 24: 291298.Google Scholar
Dimler, R. J., Schaeffer, W. C., Wise, C. S., and Rist, C. E.. 1952. Quantitative paper chromatography of D-glucose and its oligosaccharides. Analyt. Chem. 24: 14111414.CrossRefGoogle Scholar
Evans, D. R., and Barton-Browne, L.. 1960. The physiology of hunger in the blowfly. Am. Midl. Nat. 64: 282299.CrossRefGoogle Scholar
Evans, D. R., and Dethier, V. G.. 1957. The regulation of taste thresholds for sugars in the blowfly. J. Insect Physiol. 1: 317.CrossRefGoogle Scholar
Harlow, Phyllis M. 1956. A study of ovarial development and its relation to adult nutrition in the blowfly Protophormia terrae-novae (R.D.). J. exp. Biol. 33: 777797.CrossRefGoogle Scholar
Hocking, B. 1953. The intrinsic range and speed of flight of insects. Trans. R. ent. Soc. Lond. 104: 223345.Google Scholar
Hocking, B. 1968. Insect-flower associations in the high Arctic with special reference to nectar. Oikos 19: 359388.CrossRefGoogle Scholar
Lea, A. O. 1963. Some relationships between environment, corpora allata, and egg maturation in Aedine mosquitoes. J. Insect Physiol. 9: 793809.CrossRefGoogle Scholar
Lea, A. O. 1964. Studies on the dietary and endocrine regulation of autogenous reproduction in Aedes taeniorhyncus (Wied.). J. med. Ent. 1: 4044.CrossRefGoogle Scholar
Lea, A. O. 1969. Egg maturation in mosquitoes not regulated by the corpora allata. J. Insect Physiol. 15: 537541.CrossRefGoogle Scholar
Park, J. T., and Johnson, M. J.. 1949. A submicrodetermination of glucose. J. biol. Chem. 181: 149151.CrossRefGoogle ScholarPubMed
Price, R. D. 1958. Notes on the biology and laboratory colonization of Wyeomyia smithii (Coquillet) (Diptera: Culicidae). Can. Ent. 90: 473478.CrossRefGoogle Scholar
Smith, S. M., and Brust, R. A.. 1970. Autogeny and stenogamy of Aedes rempeli Vockeroth (Diptera: Culicidae) in arctic Canada. Can. Ent. 102: 253256.CrossRefGoogle Scholar
Spielman, A. 1957. The inheritance of autogeny in the Culex pipiens complex of mosquitoes. Am. J. Hyg. 65: 404425.Google ScholarPubMed
Tremblay, H. L. 1947. Biological characteristics of laboratory-reared Aedes atropalpus. J. econ. Ent. 40: 244250.CrossRefGoogle Scholar
Twohy, D. W., and Rozeboom, L. E.. 1957. A comparison of food reserves in autogenous and anautogenous Culex pipiens populations. Am. J. Hyg. 65: 316324.Google ScholarPubMed