Hostname: page-component-78c5997874-dh8gc Total loading time: 0 Render date: 2024-11-17T01:12:24.852Z Has data issue: false hasContentIssue false

Biased sex ratios and parasite mating probabilities

Published online by Cambridge University Press:  06 April 2009

R. M. May
Affiliation:
Department of Zoology, University of Oxford, South Parks Road, Oxford OX1 3PS
M. E. J. Woolhouse
Affiliation:
Department of Zoology, University of Oxford, South Parks Road, Oxford OX1 3PS

Summary

An earlier paper (May, 1977) developed a theoretical framework for exploring the consequences of dioecy for the population dynamics of schistosomes, assuming an unbiased sex ratio. This paper extends the analysis to biased sex ratios, as have been reported in practice. We consider the relationships of the mean number and distribution of worms among hosts, the sex ratio, and the mating system (monogamous or polygamous) to: (i) the female mating probability, Φ the prevalence of mated female worms. Ω: and (iii) the mean number of mated female worms per host, ξ. Among other results, we show how high values of Φ are associated with male-biased sex ratios and polygamous mating; that Ω is independent of the mating system and is relatively unaffected by the sex ratio; and that ξ is maximal for unbiased sex ratios given monogamous mating, and for female-biased sex ratios if mating is polygamous. These results, together with the confounding effects of the mean number and distribution of worms, are described in detail in the main body of the paper.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1993

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

REFERENCES

Anderson, R. M. & May, R. M. (1991). Infectious Diseases of Humans: Dynamics and Control. Oxford: Oxford University Press.CrossRefGoogle Scholar
Boulanger, D., Reid, G. D. F., Sturrock, R. F., Wolowczuk, I., Balloul, J. M., Grezel, D., Pierce, R. J., Otieno, M. F., Guerret, S., Grimaud, J. A., Butterworth, A. E. & Capron, A. (1991). Immunization of mice and baboons with recombinant Sm28GST affects both worm viability and fecundity after experimental infection with Schistosoma mansoni. Parasite Immunology 13, 473–90.CrossRefGoogle ScholarPubMed
Bradley, D. J. & May, R. M. (1978). Consequences of helminth aggregation for the dynamics of schistosomiasis. Transactions of the Royal Society of Tropical Medicine and Hygiene 72, 262–73.CrossRefGoogle ScholarPubMed
Cohen, J. E. (1977). Mathematical models of schistosomiasis. Annual Review of Ecology and Systematics 8, 209–33.CrossRefGoogle Scholar
Croll, N. A., Anderson, R. M., Gyorkos, T. W. & Ghadirian, E. (1982). The population biology and control of Ascaris lumbricoides in a rural community in Iran. Transactions of the Royal Society of Tropical Medicine and Hygiene 76, 187–97.CrossRefGoogle Scholar
Damian, R. T. & Chapman, R. W. (1983). The fecundity of Schistosoma haematobium in baboons, with evidence for a sex ratio effect. Journal of Parasitology 69, 987–9.CrossRefGoogle Scholar
Dietz, K. (1975). A pairing process. Theoretical Population Biology 8, 81–6.CrossRefGoogle ScholarPubMed
Gregory, R. D., Keymer, A. E. & Clarke, J. R. (1990). Genetics, sex and exposure: the ecology of Heligmosomoides polygyrus (Nematoda) in the wood mouse. Journal of Animal Ecology 59, 363–78.CrossRefGoogle Scholar
Liberatos, J. D. (1987). Schistosoma mansoni: male-biased sex ratios in snails and mice. Experimental Parasitology 64, 165–77.CrossRefGoogle ScholarPubMed
Macdonald, G. (1965). The dynamics of helminth infections, with special reference to schistosomes. Transactions of the Royal Society of Tropical Medicine and Hygiene 59, 489506.CrossRefGoogle ScholarPubMed
May, R. M. (1977). Togetherness among schistosomes: its effects on the dynamics of the infection. Mathematical Biosciences 35, 301–43.CrossRefGoogle Scholar
Mitchell, G. F., Garcia, E. G., Wood, S. M., Diasanta, R., Almonte, R. & Calica, E. (1990). Studies on the sex ratio of worms in schistosome infection. Parasitology 101, 2732.CrossRefGoogle Scholar
Pritchard, D. I., Quinnell, R. J., Slater, A. F. G., McKean, P. G., Dale, D. D. S., Raiko, A. & Keymer, A. E. (1990). Epidemiology and immunology of Necator americanus infection in a community in Papua New Guinea: humoral responses to excretory–secretory and cuticular collagen antigens. Parasitology 100, 317–26.CrossRefGoogle Scholar
Quinnell, R. J. (1992). The population dynamics of Heligmosomoides polygyrus in an enclosure population of wood mice. Journal of Animal Ecology 61, 669–79.CrossRefGoogle Scholar
Sturrock, R. F., Cottrell, B. J. & Kimani, R. (1984). Observations on the ability of repeated light exposures to Schistosoma mansoni cercariae to induce resistance to reinfection in Kenyan baboons (Papio anubis). Parasitology 88, 505–14.CrossRefGoogle ScholarPubMed
Theron, A., Pointier, J. P., Morand, S., Imbert—Establet, D. & Borel, G. (1992). Long-term dynamics of natural populations of Schistosoma mansoni among Rattus rattus in patchy environment. Parasitology 104, 291–8.CrossRefGoogle ScholarPubMed
Woolhouse, M. E. J., Chandiwana, S. K. & Bradley, M. (1990). Detection of overdispersion of schistosome infections of snails. International Journal for Parasitology 20, 325–7.CrossRefGoogle ScholarPubMed