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A STUDY ON ENERGETICS OF PODISUS MACULIVENTRIS (HEMIPTERA: PENTATOMIDAE)1

Published online by Cambridge University Press:  31 May 2012

M. K. Mukerji  and
E. J. LeRoux
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
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Abstract

Based on bomb calorimeter determinations, the calorific values of four sizes of larvae of Galleria mellonella (L.) fed to nymphs and adults of the predator Podisus maculiventris (Say) increased with increase in larval size. Correspondingly, these values for P. maculiventris nymphs in fourth and fifth instars and adults, male and female, increased when the predator fed on larger larvae. Increases in energy consumption resulted in increases in energy loss due to respiration and egestion for nymphs and adults of the predator. For unfed males and females, calorific values decreased with age, i.e., as initial body energy reserves were used up.No significant differences in mean calorific values were observed for fertile and infertile eggs laid by females reared at each of the four diet levels. This suggests that the amount of energy utilized by females in the production of eggs is fairly constant, irrespective of the amount of energy consumed at each diet level.Energy budgets for nymphs of P. maculiventris showed that gross efficiency of growth for second- and third-instar nymphs was inversely proportional to energy consumed; however, no such relationship was observed for fourth and fifth instars. For males, energy budgets showed that at all diet levels little growth took place during adult fife, with gross efficiency at diet levels 1 to 4 ranging from 0.88 to 2.20%. For females, some growth occurred at all levels of diet during the first 35 days of adult life, mainly as a result of the production of eggs. Gross efficiency during this period ranged from 5.5 to 13.6%. Efficiency of reproduction at diet levels 1 to 4 ranged from 37.26 to 45.35% during the first 35 days of adult life and from 39.46 to 51.16% for the next 20 days.

Type
Articles
Information
The Canadian Entomologist , Volume 101 , Issue 5 , May 1969 , pp. 449 - 460
Copyright
Copyright © Entomological Society of Canada 1969

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References

Armstrong, J. 1960. The dynamics of Dugesia tigrina populations and of Daphnia Pulex populations as modified by immigration. Ph.D. dissertation. Department of Zoology, University of Michigan, Ann Arbor.Google Scholar
Brody, S. 1945. Bioenergetics and growth. Reinhold Publishing Co., New York.Google Scholar
Clarke, G. L. 1946. Dynamics of production in a marine area. Ecol. Monogr. 16: 322–335.CrossRefGoogle Scholar
Dineen, C. C. 1953. An ecological study of a Minnesota pond. Am. Midl. Nat. 50: 349–379.CrossRefGoogle Scholar
Engelmann, M. D. 1961. The role of soil arthropods in the energetics of an old-field community. Ecol. Monogr. 31: 221–238.CrossRefGoogle Scholar
Golly, F. B. 1960. Energy dynamics of a food chain of an old-field community. Ecol. Monogr. 30: 187–206.CrossRefGoogle Scholar
Harvey, H. W. 1950. On the production of living matter in the sea off Plymouth. J. Mar. Biol. Assoc. U.K. 29: 97–137.CrossRefGoogle Scholar
Ivlev, V. W. 1939. Transformation of energy by aquatic animals. Int. Rev. d. Ges. Hydrobiol. u. Hydrogr. 38: 449–458.CrossRefGoogle Scholar
Ivlev, V. W. 1945. The biological productivity of waters. Uspekhi Souremenoi Biologii (Advances in Modern Biology) 19: 98–120. Translated by Ricker, W. E..Google Scholar
Juday, C. 1940. The annual energy budget of an inland lake. Ecology 21: 438–450.CrossRefGoogle Scholar
Lindeman, R. L. 1941. Seasonal food-cycle dynamics in a senescent lake.Am. Midl. Nat. 26: 636–673.CrossRefGoogle Scholar
Lindeman, R. L. 1942. The trophic-dynamic aspect of ecology. Ecology 23: 399–418.CrossRefGoogle Scholar
Macfadyen, A. 1948. The meaning of productivity in biological systems. J. Am. Ecol. 17: 75–80.CrossRefGoogle Scholar
Macfadyen, A. 1963. Animal ecology — aims and methods, 2nd ed.Sir Isaac Pitrnan & Sons Ltd., London.Google Scholar
Mukerji, M. K., and LeRoux, E. J.. 1969 a. The effect of predator age on the functional response of Podisus maculiventris to the prey size of Galleria mellonella. Can. Ent. 101: 314–327.CrossRefGoogle Scholar
Mukerji, M. K., and LeRoux, E. J.. 1969 b. A quantitative study of food consumption and growth of Podisus maculiventris (Hemiptera: Pentatomidae). Can. Ent. 101: 387–403.CrossRefGoogle Scholar
Odum, H. T. 1957. Trophic structure and productivity of Silver Springs, Florida. Ecol. Monogr. 27: 55–112.CrossRefGoogle Scholar
Odum, H. T., and Odum, E. P.. 1955. Trophic structure and productivity of a windward coral reef community on Eniwetok Atoll. Ecol. Monogr. 25: 291–320.CrossRefGoogle Scholar
Odum, E. P., and Smalley, A. E.. 1959. Comparison of population energy flow of a herbivorous and a deposit-feeding invertebrate in a salt marsh ecosystem. Proc. natn. Acad. Sci. 45: 617–622.CrossRefGoogle Scholar
Odum, E. P., Connell, C. E., and Davenport, L. B.. 1962. Population energy flow of three primary consumer components of old-field ecosystems. Ecology 43: 88–96.CrossRefGoogle Scholar
Parr Manual No. 128. 1958. Instructions for the No. 1411 combustion calorimeter. Parr Instrument Co., Moline, Ill.Google Scholar
Richman, S. 1958. The transformation of energy by Daphnia pulex. Ecol. Monogr. 28: 273–291.CrossRefGoogle Scholar
Ricker, W. E. 1946. Production and utilization of fish populations. Ecol. Monogr. 16: 374–391.CrossRefGoogle Scholar
Slobodkin, L. B. 1959. Energetics in Daphnia pulex populations. Ecology 40: 232–243.CrossRefGoogle Scholar
Slobodkin, L. B., and Richman, S.. 1961. Calories/gm in species of animals. Nature, Lond. 191 (4785): 299.CrossRefGoogle Scholar
Smalley, A. E. 1960. Energy flow of a salt marsh grasshopper population. Ecol. Monogr. 23: 41–72.Google Scholar
Teal, J. M. 1957. Community metabolism in a temperate cold spring. Ecol. Monogr. 23: 41–72.Google Scholar
Trama, F. B. 1957. The transformation of energy by an aquatic herbivore Stenomeae pulchellum (Ephemeroptera). Ph.D. dissertation, University of Michigan.Google Scholar
Weigert, R. G. 1964. Population energetics of meadow spittlebugs (Phibenus spumarius L.) as affected by migration and habit. Ecol. Monogr. 34: 217–241.CrossRefGoogle Scholar