9.1 INTRODUCTION Most aphid species reproduce both asexually and sexually, with several overlapping parthenogenetic generations between each period of sexual reproduction. This is known as cyclical parthenogenesis and, in temper-ate regions, sexual reproduction occurs in autumn and results in the pro-duction of over-wintering eggs, which hatch the following spring and initiate another cycle. For their size, aphids have very short developmen-tal times and potentially prodigious rates of increase and, as a conse-quence, are typically little affected by the activity of insect natural enemies (Kindlmann and Dixon, 1989; Dixon, 1992; Dixon et ai., 1995, 1997). That is, aphids show very complex and rapidly changing within-year dynamics, with each clone going through several overlapping gen-erations during the vegetative season, and potentially being made up of many individuals which can be widely scattered spatially. The produc-tion and survival rates of the eggs determine the numbers of aphids pre-sent the following spring. The study of the population dynamics of aphids living on wild herba-ceous plants is difficult because their host plants vary in abundance and distribution from year to year. Tree-living aphids, in addition to being very host specific, live in a habitat that is relatively stable both spatially and temporally. Therefore, it is not surprising that most long-term popu-lation studies on aphids have been on tree-dwelling species. The studies on deciduous tree-dwelling species
CITATION STYLE
Dixon, A. F. G., & Kindlmann, P. (1998). Population dynamics of aphids. In Insect Populations In theory and in practice (pp. 207–230). Springer Netherlands. https://doi.org/10.1007/978-94-011-4914-3_9
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