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Experimental population dynamics of Rhabdias bufonis (Nematoda) in toads (Bufo bufo): density-dependence in the primary infection

Published online by Cambridge University Press:  06 April 2009

C. P. Goater
Affiliation:
Zoologisches Museum der Universität Zürich, Winterthurerstrasse 190, 8057 Zürich, Switzerland

Summary

Density-dependence in worm establishment, numbers, biomass and larval production were examined in primary infections of 0, 10, 40, 80 and 160 larvae of the lung nematode, Rhabdias bufonis in the common toad, Bufo bufo. The infection procedure established 4 non-overlapping levels of infection which persisted until 6 weeks post-infection (p.i.), after which there was an overall decline up to 12 weeks p.i. Worm numbers had no direct effect on adult worm survival but temporal changes in worm weight were density-dependent. Adult worm establishment in the lungs declined significantly as the numbers of worms in the lungs increased. At the lowest exposure dose, 86% of the larvae administered reached maturity in the lungs while at the highest, only 37% did so. Also, the numbers of immature larvae outside the lungs increased as adult worm numbers increased. Both features provide evidence for a threshold limit to the numbers of worms maturing in the lungs. Worm numbers also affected larval output per host and per capita fecundity. A significant positive relationship between per capita fecundity and per capita worm weight suggested that density-dependence acted primarily to constrain the growth of individual worms. Finally, the constraints imposed on worm growth and fecundity were apparently relaxed when worm density decreased, providing evidence for density-dependent flexibility in per capita fecundity. Density-dependence in worm establishment and per capita fecundity are mechanisms which may potentially regulate this host–parasite interaction in the field. Both mechanisms may be functionally related to physical space limitations in the lungs, within which worms must compete for finite nutrients.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1992

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References

REFERENCES

Alford, R. A. & Harris, R. N. (1988). Effects of larval growth history on anuran metamorphosis. American Naturalist 131, 91106.CrossRefGoogle Scholar
Anderson, R. M. (1982). Epidemiology. In Modern Parasitology (ed. Cox, F. E. G), pp. 204–51. London: Blackwell Scientific Publications.Google Scholar
Anderson, R. M. & Gordon, D. M. (1982). Processes influencing the distribution of parasite numbers within host populations with special emphasis on parasite-induced host mortalities. Parasitology 85, 373–98.CrossRefGoogle ScholarPubMed
Anderson, R. M. & May, R. M. (1978). Regulation and stability of host–parasite population interactions. I. Regulatory processes. Journal of Animal Ecology 47, 219–47.Google Scholar
Chappell, L. H. & Pike, A. W. (1976). Loss of Hymenolepis diminuta from the rat. International Journal for Parasitology 6, 33–9.Google Scholar
Cox, F. E. G. (1971). Parasites of British amphibians. Journal of Biological Education 5, 3551.Google Scholar
Crofton, H. D. (1971). A quantitative approach to parasitism. Parasitology 62, 179–94.CrossRefGoogle Scholar
Crompton, D. W. T. (1984). Influence of parasitic infection on host food intake. Federation Proceedings 43, 239–45.Google Scholar
Frandsen, F. (1974). A study of Danish amphibian parasite fauna. Acta Parasitologica Polonica 22, 4966.Google Scholar
Goater, C. P. & Ward, P. I. (1992). Negative effects of Rhabdias bufonis (Nematoda) on the growth and survival of juvenile toads, Bufo bufo. Oecologia (in the Press).Google Scholar
Jackson, H. C. & Tinsley, R. C. (1988). Environmental influences on egg production by the mongenean Protopolystoma xenopodis. Parasitology 97, 115–28.Google Scholar
Kennedy, C. R. (1975). Ecological Animal Parasitology. London: Blackwell Scientific Publications.Google Scholar
Kennedy, C. R. (1984). The use of frequency distributions in an attempt to detect host mortality induced by infections of diplostomatid metacercariae. Parasitology 89, 209–20.Google Scholar
Kennedy, C. R. (1987). Long-term stability in the population levels of the eyefluke Tylodelphys podicipina (Digenea: Diplostomatidae) in perch. Journal of Fish Biology 31, 571–81.Google Scholar
Keymer, A. E. (1982). Density-dependent mechanisms in the regulation of intestinal helminth populations. Parasitology 84, 573–87.Google Scholar
Keymer, A. E. & Hiorns, R. W. (1986). Faecal egg counts and nematode fecundity: Heligmosomoides polygyrus and laboratory mice. Parasitology 93, 189203.Google Scholar
Keymer, A. E. & Slater, A. F. G. (1987). Helminth fecundity: density dependence or statistical illusion? Parasitology Today 3, 56–8.CrossRefGoogle ScholarPubMed
Kozak, A. (1973). The nematode fauna of frogs in the Carpathean region of Czechoslovakia. Biologia 28, 325–34.Google Scholar
Michael, E. & Bundy, D. A. P. (1989). Density-dependence in establishment, growth and worm fecundity in intestinal helminthiasis: the population biology of Trichuris muris (Nematoda) infection in CBA/Ca mice. Parasitology 98, 451–8.Google Scholar
Moss, G. D. (1971). The nature of the immune response of the mouse to the bile duct cestode, Hymenolepis microstoma. Parasitology 62, 285–94.Google Scholar
Plasota, K. (1969). The effect of some ecological factors on the parasitofauna of frogs. Acta Parasitologica Polonica 16, 4760.Google Scholar
Smyth, J. D. & Smyth, M. M. (1980). Frogs as Host–Parasite Systems. London: Macmillan Press.CrossRefGoogle Scholar
Tinsley, R. C. (1989). The effects of host sex on transmission success. Parasitology Today 5, 190–5.Google Scholar
Tocque, K. & Tinsley, R. C. (1991). Asymmetric reproductive output by the mongenean Pseudodiplorchis americanus. Parasitology 102, 213–20.Google Scholar
Yong, K. & Dobson, C. (1982). Population dynamics of Angiostrongylus cantonensis during primary infection in rats. Parasitology 85, 399409.Google Scholar