Hostname: page-component-78c5997874-v9fdk Total loading time: 0 Render date: 2024-11-10T08:02:12.653Z Has data issue: false hasContentIssue false

Some Maternal Influences on Progeny Quality in the Western Tent Caterpillar, Malacosoma pluviale (Dyar)1

Published online by Cambridge University Press:  31 May 2012

W. G. Wellington
Affiliation:
Forest Entomology and Pathology Laboratory, Victoria, British Columbia

Abstract

The different types of individuals among the progeny of the western tent caterpillar, Malacosoma pluviale (Dyar), are concentrated in different parts of the egg mass. The most agile progeny come from some of the first eggs laid, and the least viable are among the last deposited. There is evidence that this serial arrangement stems from unequal partitioning of the maternal food reserves during egg production: a relationship similar to that recently demonstrated in the spruce budworm by I. M. Campbell. In M. pluviale, however, there also is evidence that the differences in feeding rate and food capacity displayed by the different types of females during their own larval stage affect the proportions of the various types of progeny per egg mass as well as the viability of consecutive groups of eggs within the mass. Although these maternal influences are not heritable in the usual genetic sense, they are clearly transmissible between generations. And field studies have shown that their more adverse consequences for local populations are cumulative and ultimately lethal.

Type
Articles
Copyright
Copyright © Entomological Society of Canada 1965

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Albrecht, F. O. 1962. Some physiological and ecological aspects of locust phases. Trans. R. ent. Soc. Lond. 114: 335375.Google Scholar
Campbell, I. M. 1962. Reproductive capacity in the genus Choristoneura Led. (Lepidoptera: Tortricidae). I. Quantitative inheritance and genes as controllers of rates. Canad. J. Genet. Cytol. 4: 272288.CrossRefGoogle Scholar
Campbell, I. M., and Sullivan, C. R.. 1963. Effect of temperature on egg production in Neodriprion sertifer (Geoff.) (Hymenoptera: Diprionidae). Proc. XVI int. Congr. Zool. 2: 62.Google Scholar
Richards, A. G. 1959. Studies on temperature thresholds in insect development. Biol. Zentralbl. 78: 308314.Google Scholar
Taber, S. III, and Roberts, W. C.. 1963. Egg weight variability and its inheritance in the honey bee. Ann. ent. Soc. Amer. 56: 473476.CrossRefGoogle Scholar
Turnbull, A. L. 1962. Quantitative studies of the food of Linyphia triangularis Clerck (Araneae: Linyphiidae). Canad. Ent. 94: 12331249.Google Scholar
Wellington, W. G. 1957. Individual differences as a factor in population dynamics: the development of a problem. Canad. J. Zool. 35: 293323.CrossRefGoogle Scholar
Wellington, W. G. 1959. Individual differences in larvae and egg masses of the western tent caterpillar. Can. Dep. Agric. For. Biol. Div. Bi-m. Prog. Rep. 15: 34.Google Scholar
Wellington, W. G. 1960. Qualitative changes in natural populations during changes in abundance. Canad. J. Zool. 38: 289314.Google Scholar
Wellington, W. G. 1962. Population quality and the maintenance of nuclear polyhedrosis between outbreaks of Malacosoma pluviale (Dyar). J. Ins. Pathol. 4: 285305.Google Scholar
Wellington, W. G. 1964. Qualitative changes in populations in unstable environments. Canad. Ent. 96: 436451.CrossRefGoogle Scholar