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A QUANTITATIVE STUDY OF FOOD CONSUMPTION AND GROWTH OF PODISUS MACULIVENTRIS (HEMIPTERA: PENTATOMIDAE)1

Published online by Cambridge University Press:  31 May 2012

M. K. Mukerji
Affiliation:
Department of Entomology, Macdonald College of McGill University, Macdonald College P.O., Quebec
E. J. LeRoux
Affiliation:
Department of Entomology, Macdonald College of McGill University, Macdonald College P.O., Quebec

Abstract

Nymphs and adults of Podisus maculiventris (Say), reared on four sizes (diet levels) of live larvae of Galleria mellonella (L.), captured prey, consumed food, and grew at rates varying with the size of larvae supplied. For nymphs, a direct linear relationship was obtained between rate of food consumption and daily growth and rate of food consumption and daily development. For adults, male and female, age did not affect food intake significantly, but for females alone, food intake differed significantly at different diet levels. A significant difference was also obtained for both sexes between body weight and diet level. Males and females lived longest on diet 1, apparently because of reduced metabolic activity.The number of eggs laid by each female corresponded to its food consumption for the first 35 days but decreased thereafter with age. The mean dry weights for fertile and infertile eggs at different diet levels did not differ significantly irrespective of the amount of food consumed by egg-laying females.For each nymph in each of instars 2 to 5 and for adults, the consumption quotient, an index of metabolic activity, increased as the rate of food consumption increased. For nymphs, the quotient decreased during ontogeny at each diet level, and for adults, decreased with age at diet levels 2, 3, and 4. The quotient remained constant for adults of both sexes at diet level 1.Results show that nymphs and adults of P. maculiventris can survive and mature satisfactorily for extended periods on small prey but needs larger prey to accelerate development, increase growth, and maintain a high reproductive potential.

Type
Articles
Copyright
Copyright © Entomological Society of Canada 1969

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References

Balogh, J. 1953. Grundzüge der Zoozönologie. Budapest.Google Scholar
Couturier, A. 1938. Contribution à l'étude biologique de Podisus maculiventris (Say) prédateur américain du doryphore. Ann. des Épiphyties et de Phytogénétique (N.S.) 4: 95165.Google Scholar
Dunger, W. 1958. Über die Zersetzung der Laubstren durch die Boden-Makrofauna in Auenwald. Zool. Jber. (Syst.) 86: 139180.Google Scholar
Gere, G. 1956. The examination of the feeding biology and humificative function of Diplopoda and Isopoda. Acta Biol. Univ. Szeged. 6: 257271.Google Scholar
LeRoux, E. J. 1964. The application of ecological principles to orchard Entomology in Canada. Can. Ent. 96: 348356.CrossRefGoogle Scholar
Morrill, A. W. 1906. Some observations on the spined soldier bug (Podisus maculiventris Say). U.S. Div. Ent. Bull. (N.S.) 60: 155161.Google Scholar
Morris, R. F. 1963. The effect of predator age and prey defence on the functional response of Podisus maculiventris (Say) to the density of Hyphantria cunea (Drury). Can. Ent. 95: 10091020.CrossRefGoogle Scholar
Mukerji, M. K., and LeRoux, E. J.. 1965. Laboratory rearing of a Quebec strain of the pentatomid predator, Podisus maculiventris (Say) (Hemiptera: Pentatomidae). Phytoprotection 46: 4060.Google Scholar
Mukerji, M. K., and LeRoux, E. J.. 1969. The effect of predator age on the functional response of Podisus maculiventris to the prey size of Galleria mellonella. Can. Ent. 101: 314327.CrossRefGoogle Scholar
Mukerji, M. K., and LeRoux, E. J.. In press. A study on energetics of Podisus maculiventris (Hemiptera: Pentatomidae). Can. Ent.Google Scholar
Nicholson, A. J. 1950. Population oscillations caused by competition for food. Nature, Lond. 165: 476477.CrossRefGoogle Scholar
Phillipson, J. 1960. The food consumption of different instars of Mitopus morio (F.) (Phalangida) under natural conditions. J. Anim. Ecol. 29: 299307.CrossRefGoogle Scholar
Turnbull, A. L. 1962. Quantitative studies of the food of Linyphia triangularis Clerck (Araneae: Linyphiidae). Can. Ent. 94: 12331249.CrossRefGoogle Scholar
Turnbull, A. L. 1965. Effects of prey abundance on the development of the spider Agelenopsis potteri (Blackwall) (Aranea: Agelenidae). Can. Ent. 97: 141147.CrossRefGoogle Scholar
Ullyett, G. C. 1950. Competition for food and allied phenomena in sheep blowfly populations. Phil. Trans. R. Soc. Lond. B 234: 77174.Google Scholar
van der Drift, J. 1951. Analysis of the animal community in a beech forest floor. Tijdschr. Ent. 94: 1168.Google Scholar
Zeuthen, E. 1947. Body size and metabolic rate in the animal kingdom with special regard to the marine microfauna. Comp. Rendus Lab. Carlsberg Ser. Chem. 26: 17161.Google Scholar