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Seasonal abundance of Proteocephalus ambloplitis (Cestoidea: Proteocephalidea) from largemouth bass living in a heated reservoir

Published online by Cambridge University Press:  06 April 2009

Herman Eure
Herman Eure
Affiliation:
Savannah River Ecology Laboratory, Aiken, S.C. 29801, and Department of Biology, Wake Forest University, Winston-Salem, N.C. 27109, U.S.A.
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Extract

Proteocephalus ambloplitis was recovered from largemouth bass inhabiting different thermal regimes, ranging from normal to greater than 10 °C above normal, on the Energy Research and Development Administration's (ERDA) Savannah River Plant near Aiken, South Carolina. Possible alterations in the mechanisms initiating plerocercoid migration as proposed by Fischer & Freeman (1969) were noted. According to these authors, a rise in temperature from 4 to 7 °C and above stimulated migration of parenteric plerocercoids into the gut. The lowest water temperature recorded for the reservoir for the entire sampling period was 8·0 °C. Theoretically, this should have terminated the life-cycle of this tapeworm since migration temperature was never attained. At Savannah River, the appearance of adult tapeworms coincided with a decrease in water temperature, while the appearance of adult tapeworms in Canada was correlated with an increase in water temperature. It is postulated that the decline in water temperature in southern latitudes and the increase in water temperature in northern latitudes initiates the same response, that is, migration of plerocercoids from parenteric to enteric sites where maturation to the adult form ensues.

Type
Research Article
Information
Parasitology , Volume 73 , Issue 2 , October 1976 , pp. 205 - 212
Copyright
Copyright © Cambridge University Press 1976

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References

REFERENCES

Bennett, D. H. (1971). Preliminary examination of body temperatures of largemouth bass (Micropterus salmoidea) from an artificially heated reservoir. Archiv für Hydrobiologie 68, 376–81.Google Scholar
Bennett, D. H. (1972). Length-weight relationships and condition factors of fishes from a South Carolina reservoir receiving thermal effluent. Progressive Fish Culturist 34, 85–7.CrossRefGoogle Scholar
Boyd, C. E. (1970). Production, mineral accumulation and pigment concentrations of Typha latifolia and Scirpus americanua. Ecology 51, 285–90.CrossRefGoogle Scholar
Brisbin, I. L Jr. (1974). Abundance and diversity of waterfowl inhabiting heated and non-heated portions of a reactor cooling reservoir. In Thermal Ecology (ed. Gibbons, J. W. and Sharitz, R. R.), pp. 579–93. AEC Symposium Series (CONF-730505).Google Scholar
Chappell, L. H. (1969). The parasites of the three-spined stickleback Gasterosteus aculeatus L. from a Yorkshire pond. I. Seasonal variation of parasite fauna. Journal of Fish Biology 1, 137–52.CrossRefGoogle Scholar
Esch, G. W, Johnson, W. C. & Coggins, J. R. (1975). Studies on the population biology of Proteocephalus ambloplitis (Cestoda) in the smallmouth bass. Proceedings of the Oklahoma Academy of Science 55, 122–7.Google Scholar
Fischer, H. & Freeman, R. S. (1969). Penetration of parenteral plerocercoids of Proteocephalus ambloplitis (Leidy) into the gut of smalknouth bass. Journal of Parasitology 55, 766–74.CrossRefGoogle Scholar
Gibbons, J. W. (1970). Terrestrial activity and the population dynamics of aquatic turtles. American Midland Naturalist 83, 404–14.CrossRefGoogle Scholar
Goodnight, J. & Barr, J. (1971). User's Guide to the Statistical Analysis System. N.C. State University, Raleigh, N.C.Google Scholar
Hopkins, C. A. (1959). Seasonal variation in the incidence and development of the cestode Proteocephaltis filicollis (Rud. 1810) in Gasterosteus aculeatus (L. 1766). Parasitology 49, 529–42.CrossRefGoogle ScholarPubMed
Hunter, G. W. (1928). Contributions to the life history of Proteocephalua ambloplitis (Leidy). Journal of Parasitology 14, 229–42.CrossRefGoogle Scholar
Nelson, D. H. (1974). Responses of larval amphibian populations to heated effluents in a southeastern reservoir. In Thermal Ecology, (ed. Gibbons, J. W. and Sharitz, R. R.), pp. 264–76. AEC Symposium Series (CONF-730505).Google Scholar
Scheffe, H. (1959). The Analysis of Variance. New York: Wiley.Google Scholar
Sokal, R. & Rohlf, F. (1969). Biometry. San Francisco: W. H. Freeman.Google Scholar