Parasites, sex, and clonal diversity in natural snail populations

Evolution

Volumn 65, Issue 5, 2011, Pages 1474-1481

  King, Kayla C ^a   Jokela, Jukka ^b,c   Lively, Curtis M ^a  

^a INDIANA UNIVERSITY   (United States)

^b SWISS FEDERAL INSTITUTE OF AQUATIC SCIENCE AND TECHNOLOGY   (Switzerland)

^c ETH ZURICH   (Switzerland)

Author keywords

Clonal diversity; Frequency dependent selection; Host parasite coevolution; Red queen hypothesis

Indexed keywords

CLONAL GROWTH; COEVOLUTION; CONSPECIFIC; FREQUENCY DEPENDENCE; GENETIC VARIATION; HOST-PARASITE INTERACTION; MUTATION; PARTHENOGENESIS; RED QUEEN HYPOTHESIS; SEXUAL REPRODUCTION; SNAIL;

ADAPTATION; ANIMAL; ARTICLE; EVOLUTION; FEMALE; GENETIC VARIABILITY; GENOTYPE; HOST PARASITE INTERACTION; MALE; NEW ZEALAND; PARASITOLOGY; PARTHENOGENESIS; PHYSIOLOGY; POPULATION DYNAMICS; REPRODUCTION; SNAIL; TREMATODE;

ADAPTATION, PHYSIOLOGICAL; ANIMALS; BIOLOGICAL EVOLUTION; FEMALE; GENETIC VARIATION; GENOTYPE; HOST-PARASITE INTERACTIONS; MALE; NEW ZEALAND; PARTHENOGENESIS; POPULATION DYNAMICS; REPRODUCTION; SNAILS; TREMATODA;

ANIMALIA; GASTROPODA;

EID: 79955136138     PISSN: 00143820     EISSN: 15585646     Source Type: Journal    
DOI: 10.1111/j.1558-5646.2010.01215.x     Document Type: Article

References (38)

1. Bell, G. 1982. The masterpiece of nature: the evolution and genetics of asexuality. Univ. of California Press, Berkeley, CA.
2. Bérénos, C., K. M. Wegner, and P. Schmid-Hempel 2011. Antagonistic coevolution with parasites maintains host genetic diversity: an experimental test. Proc. R. Soc. Biol. Sci. B. In press
3. Brown, M. J. F., and P. Schmid-Hempel 2003. The evolution of female multiple mating in social hymenoptera. Evolution 57:2067-2081.
4. D'Souza, T. G., and N. K. Michiels 2006. Genetic signatures of occasional sex in parthenogenetic subpopulations of the freshwater planarianSchimidtea polychroa. Freshw. Biol. 51:1890-1900.
5. Duffy, M., C. E. Brassil, S. R. Hall, A. J. Tessier, C. E. Caceres, and J. K. Conner 2008. Parasite-mediated disruptive selection in a naturalDaphniapopulation. BMC Evol. Biol. 8:80-88.
6. Duncan, A. B., and T. J. Little 2007. Parasite-driven genetic change in a natural population ofDaphnia. Evolution 61:796-803.
7. Dybdahl, M. F., and C. M. Lively 1995a. Diverse, endemic, and polyphyletic clones in mixed populations of a freshwater snail (Potamopyrgus antipodarum). J. Evol. Biol. 8:385-398.
8. Dybdahl, M. F., and C. M. Lively 1995b. Host-parasite interactions: infection of common clones in natural populations of a freshwater snail (Potamopyrgus antipodarum). Proc. R. Soc. Biol. Sci. Ser. B 260:99-103.
9. Dybdahl, M. F., and C. M. Lively 1998. Host-parasite coevolution: evidence for rare advantage and time-lagged selection in a natural population. Evolution 52:1057-1066.
10. Fox, J. A., M. F. Dybdahl, J. Jokela, and C. M. Lively 1996. Genetic structure of coexisting sexual and clonal subpopulations in a freshwater snail (Potamopyrgus antipodarum). Evolution 50:1541-1548.
11. Haldane, J. B. S. 1949. Disease and evolution. La ricerca Scientifica 19:68-76.
12. Hamilton, W. D. 1980. Sex versus non-sex versus parasite. Oikos 35:282-290.
13. Hamilton, W. D., R. Axelrod, and R. Tanese 1990. Sexual reproduction as an adaptation to resist parasites (a review). Proc. Natl. Acad. Sci. USA 87:3566-3573.
14. Howard, S. R., and C. M. Lively 1998. The maintenance of sex by parasitism and mutation accumulation under epistatic fitness functions. Evolution 52:604-610.
15. Jaenike, J. 1978. An hypothesis to account for the maintenance of sex within populations. Evol. Theory 3:191-194.
16. Jokela, J., and C. M. Lively 1995. Spatial variation in infection by digenetic trematodes in a population of freshwater snails (Potamopyrgus antipodarum). Oecologia 103:509-517.
17. Jokela, J., M. F. Dybdahl, and C. M. Lively 2009. The maintenance of sex, clonal dynamics, and host-parasite coevolution in a mixed population of sexual and asexual snails. Am. Nat. 174:S43-S53.
18. King, K. C., and C. M. Lively 2009. Geographic variation of sterilizing parasite species and the Red Queen. Oikos 118:1416-1420.
19. Koskella, B., and C. M. Lively 2009. Evidence for negative frequency-dependent selection during experimental coevolution of a freshwater snail and a sterilizing trematode. Evolution 63:2213-2221.
20. Legendre, P., and L. Legendre 1998. Numerical ecology. Elsevier Science, Amsterdam
21. Lewontin, R. C. 1974. The genetic basis of evolutionary change. Columbia Univ. Press, New York
22. Lively, C. M. 1987. Evidence from a New Zealand snail for the maintenance of sex by parasitism. Nature 328:519-521.
23. Lively, C. M., and R. S. Howard 1994. Selection by parasites for clonal diversity and mixed mating. Philos. Trans. R. Soc. Lond. B 346:271-281.
24. Lively, C. M., and M. F. Dybdahl 2000. Parasite adaptation to locally common host genotypes. Nature 405:679-681.
25. Lively, C. M., and J. Jokela 2002. Temporal and spatial distributions of parasites and sex in a freshwater snail. Evol. Ecol. Res. 4:219-226.
26. Neiman, M., J. Jokela, and C. M. Lively 2005. Variation in asexual lineage age inPotamopyrgus antipodarum, a New Zealand snail. Evolution 59:1945-1952.
27. Neiman, M., S. Meirmans, and P. G. Meirmans 2009. What can asexual lineage age tell us about the maintenance of sex Ann. N. Y. Acad. Sci. 1168:185-200.
28. Neiman, M., G. Hehman, J. T. Miller, J. M. J. Jogsdon, and D. R. Taylor 2010. Accelerated mutation accumulation in asexual lineages of a freshwater snail. Mol. Biol. Evol. 27:954-963.
29. Nevo, E. 1978. Genetic variation in natural populations: patterns and theory. Theor. Popul. Biol. 13:121-177.
30. Schmid-Hempel, P. 1994. Infection and colony variability in social insects. Philos. Trans. R. Soc. Lond. B 346:313-321.
31. Schmid-Hempel, P., and R. H. Crozier 1999. Polygyny versus polyandry versus parasites. Philos. Trans. R. Soc. Lond. B 354:507-515.
32. Simon, J.-C., F. Delmotte, C. Rispe, and T. Crease 2003. Phylogenetic relationships between parthenogens and their sexual relatives: the possible routes to parthenogenesis in animals. Biol. J. Linn. Soc. 79:151-163.
33. Stoddart, J. A., and J. F. Taylor 1988. Genotypic diversity: estimation and prediction in samples. Genetics 118:705-711.
34. Vorburger, C. 2006. Temporal dynamics of genotypic diversity reveal strong clonal selection in the aphidMyzus persicae. J. Evol. Biol. 19:97-107.
35. Vrijenhoek, R. C. 1998. Animal clones and diversity. Bioscience 48:617-628.
36. Wallace, C. 1992. Parthenogenesis, sex and chromosomes inPotamopyrgus. J. of Molluscan Studies 58:93-107.
37. Winterbourn, M. J. 1974. Larval trematoda parasitizing the New Zealand species ofPotamopyrgus(Gastropoda: Hydrobiidae). Mauri Ora 2:17-30.
38. Wolinska, J., and P. Spaak 2009. The cost of being common: evidence from naturalDaphniapopulations. Evolution 63:1893-1901.