The cybrid invasion: Widespread postglacial dispersal by phoxinus (Pisces: Cyprinidae) cytoplasmic hybrids

Canadian Journal of Zoology

Volumn 90, Issue 5, 2012, Pages 577-584

  Mee, J A ^a,b   Taylor, E B ^a  

^a UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^b UNIVERSITY OF CALGARY   (Canada)

Author keywords

Cybrids; Finescale dace; Gynogenesis; Hybrid species; Maintenance of sex; Mitochondrial introgression; Northern redbelly dace; Phoxinus eos; Phoxinus eos neogaeus; Phoxinus neogaeus; Sperm dependent asexual reproduction

Indexed keywords

ASEXUAL REPRODUCTION; BIOTYPE; COEXISTENCE; CYPRINID; CYTOPLASM; FITNESS; GENOME; HYBRID; INTROGRESSION; LIFE HISTORY TRAIT; MITOCHONDRIAL DNA; REPRODUCTIVE COST; SAMPLING;

CANADA;

CYPRINIDAE; CYPRINIFORMES; PHOXINUS; PHOXINUS EOS; PHOXINUS EOS-NEOGAEUS; PHOXINUS NEOGAEUS; PISCES;

EID: 84860337902     PISSN: 00084301     EISSN: 14803283     Source Type: Journal    
DOI: 10.1139/Z2012-023     Document Type: Article

References (42)

1. Angers, B., and Schlosser, I.J. 2007. The origin of Phoxinus eosneogaeus unisexual hybrids. Mol. Ecol. 16(21): 4562-4571. doi:10.1111/j.1365-294X.2007.03511.x. PMID:17892466.
2. Avise, J.C. 2008. Clonality: the genetics, ecology, and evolution of sexual abstinence in vertebrates. Oxford University Press, Oxford.
3. Avise, J.C. 2009. Phylogeography: retrospect and prospect. J. Biogeogr. 36(1): 3-15. doi:10.1111/j.1365-2699.2008.02032.x.
4. Bailey, R.M., and Smith, G.R. 1981. Origin and geography of the fish fauna of the Laurentian Great Lakes basin. Can. J. Fish. Aquat. Sci. 38(12): 1539-1561. doi:10.1139/f81-206.
5. Bernatchez, L. 1997. Mitochondrial DNA analysis confirms the existence of two glacial races of rainbow smelt Osmerus mordax and their reproductive isolation in the St. Lawrence River estuary (Quebec, Canada). Mol. Ecol. 6(1): 73-83. doi:10.1046/j.1365294X.1997.00156.x.
6. Bernatchez, L., Glemet, H., Wilson, C.C., and Danzmann, R.G. 1995. Introgression and fixation of arctic char (Salvelinus alpinus) mitochondrial genome in an allopatric population of brook trout (Salvelinus fontinalis). Can. J. Fish. Aquat. Sci. 52(1): 179-185. doi:10.1139/f95-018.
7. Binet, M.C., and Angers, B. 2005. Genetic identification of members of the Phoxinus eos-neogaeus hybrid complex. J. Fish Biol. 67(4): 1169-1177. doi:10.1111/j.0022-1112.2005.00802.x.
8. Clement, M., Posada, D., and Crandall, K.A. 2000. TCS: a computer program to estimate gene geneologies. Mol. Ecol. 9(10): 1657-1659. doi:10.1046/j.1365-294x.2000.01020.x. PMID:11050560.
9. Côté, G., Perry, G., Blier, P., and Bernatchez, L. 2007. The influence of gene-environment interactions on GHR and IGF-I expression and their association with growth in brook charr, Salvelinus fontinalis (Mitchill). BMC Genet. 8: 87. doi:10.1186/1471-2156-8-87.
10. Dawley, R.M., and Bogart, J.P. (Editors). 1989. Evolution and ecology of unisexual vertebrates. New York State Education Department, Albany.
11. Doeringsfeld, M.R., Schlosser, I.J., Elder, J.F., and Evenson, D.P. 2004. Phenotypic consequences of genetic variation in a gynogenetic complex of Phoxinus eos-neogaeus clonal fish (Pisces: Cyprinidae) inhabiting a heterogeneous environment. Evolution, 58(6): 1261-1273. PMID:15266975.
12. Doiron, S., Bernatchez, L., and Blier, P.U. 2002. A comparative mitogenomic analysis of the potential adaptive value of arctic charr mtDNA introgression in brook charr populations (Salvelinus fontinalis Mitchill). Mol. Biol. Evol. 19(11): 1902-1909. doi:10. 1093/oxfordjournals.molbev.a004014. PMID:12411599.
13. Engeler, B., and Reyer, H.U. 2001. Choosy females and indiscriminate males: mate choice in mixed populations of sexual and hybridogenetic water frogs (Rana lessonae, Rana esculenta). Behav. Ecol. 12(5): 600-606. doi:10.1093/beheco/12.5.600.
14. Glemet, H., Blier, P., and Bernatchez, L. 1998. Geographical extent of Arctic char (Salvelinus alpinus) mtDNA introgression in brook char populations (S. fontinalis) from eastern Quebec, Canada. Mol. Ecol. 7(12): 1655-1662. doi:10.1046/j.1365-294x.1998.00494.x.
15. Goddard, K.A., and Schultz, R.J. 1993. Aclonal reproduction by polyploid members of the clonal hybrid species Phoxinus eosneogaeus (Cyprinidae). Copeia, 1993(3): 650-660. doi:10.2307/ 1447226.
16. Goddard, K.A., Megwinoff, O., Wessner, L.L., and Giaimo, F. 1998. Confirmation of gynogenesis in Phoxinus eos-neogaeus (Pisces: Cyprinidae). J. Hered. 89(2): 151-157. doi:10.1093/jhered/89.2.151.
17. Hellriegel, B., and Reyer, H.U. 2000. Factors influencing the composition of mixed populations of a hemiclonal hybrid and its sexual host. J. Evol. Biol. 13(6): 906-918. doi:10.1046/j.14209101.2000.00235.x.
18. Heubel, K.U., Rankin, D.J., and Kokko, H. 2009. How to go extinct by mating too much: population consequences of male mate choice and efficiency in a sexual-asexual species complex. Oikos, 118(4): 513-520.
19. Lannig, G., Storch, D., and Portner, H.O. 2005. Aerobic mitochondrial capacities in Antarctic and temperate eelpout (Zoarcidae) subjected to warm versus cold acclimation. Polar Biol. 28(8): 575-584. doi:10.1007/s00300-005-0730-9.
20. Legendre, P., and Legendre, V. 1984. Postglacial dispersal of freshwater fishes in the Québec peninsula. Can. J. Fish. Aquat. Sci. 41(12): 1781-1802. doi:10.1139/f84-220.
21. Lively, C.M. 1996. Host-parasite coevolution and sex. Bioscience, 46(2): 107-114. doi:10.2307/1312813.
22. Lively, C.M., Craddock, C., and Vrijenhoek, R.C. 1990. Red Queen hypothesis supported by parasitism in sexual and clonal fish. Nature, 344(6269): 864-866. doi:10.1038/344864a0.
23. Loyning, M.K. 2000. Reproductive performance of clonal and sexual bark beetles (Coleoptera: Scolytidae) in the field. J. Evol. Biol. 13(5): 743-748. doi:10.1046/j.1420-9101.2000.00227.x.
24. Lucassen, M., Koschnick, N., Eckerle, L.G., and Portner, H.O. 2006. Mitochondrial mechanisms of cold adaptation in cod (Gadus morhua L.) populations from different climatic zones. J. Exp. Biol. 209(13): 2462-2471. doi:10.1242/jeb.02268. PMID:16788029.
25. Mandrak, N.E., and Crossman, E.J. 1992. Postglacial dispersal of freshwater fishes into Ontario. Can. J. Zool. 70(11): 2247-2259. doi:10.1139/z92-302.
26. McPhail, J.D., and Lindsey, C.C. 1970. Freshwater fishes of northwestern Canada and Alaska. Fish. Res. Board Can. 173: 7-26.
27. Mee, J.A., and Otto, S.P. 2010. Variation in the strength of male mate choice allows long-term coexistence of sperm-dependent asexuals and their sexual hosts. Evolution, 64(10): 2808-2819. PMID: 20550576.
28. Mee, J.A., and Rowe, L. 2006. A comparison of parasite loads on asexual and sexual Phoxinus (Pisces: Cyprinidae). Can. J. Zool. 84(6): 808-816. doi:10.1139/z06-064.
29. Mee, J.A., Brauner, C.J., and Taylor, E.B. 2011. Repeat swimming performance and its implications for inferring the relative fitness of asexual hybrid dace (Pisces: Phoxinus) and their sexually reproducing parental species. Physiol. Biochem. Zool. 84(3): 306-315. doi:10.1086/659245. PMID:21527822.
30. Moore, W.S. 1976. Components of fitness in a unisexual fish Poeciliopsis monacha-occidentalis. Evolution, 30(3): 564-578. doi:10.2307/2407580.
31. Moore, W.S., and McKay, F.E. 1971. Coexistence in unisexual-bisexual species complexes of Poeciliopsis (Pisces: Poeciliidae). Ecology, 52(5): 791-799. doi:10.2307/1936026.
32. Moritz, C., McCallum, H., Donnellan, S., and Roberts, J.D. 1991. Parasite loads in parthenogenetic and sexual lizards (Heteronotia binoei): support for the Red Queen Hypothesis. Proc. R. Soc. Lond. B Biol. Sci. 244(1310): 145-149. doi:10.1098/rspb.1991.0063.
33. Quattro, J.M., Avise, J.C., and Vrijenhoek, R.C. 1991. Molecular evidence for multiple origins of hybridogenetic fish clones (Poeciliidae, Poeciliopsis). Genetics, 127(2): 391-398. PMID: 2004710.
34. Rambaut, A. 2002. Sequence alignment editor. Version 2.0a11 [computer program]. Department of Zoology, University of Oxford, Oxford, U.K.
35. Redenbach, Z., and Taylor, E.B. 2002. Evidence for historical introgression along a contact zone between two species of char (Pisces: Salmonidae) in northwestern North America. Evolution, 56(5): 1021-1035. PMID:12093016.
36. Schlosser, I.J., Doeringsfeld, M.R., Elder, J.F., and Arzayus, L.F. 1998. Niche relationships of clonal and sexual fish in a heterogeneous landscape. Ecology, 79(3): 953-968. doi:10.1890/ 0012-9658(1998)079[0953:NROCAS]2.0.CO;2.
37. Schlupp, I. 2005. The evolutionary ecology of gynogenesis. Annu. Rev. Ecol. Evol. Syst. 36(1): 399-417. doi:10.1146/annurev. ecolsys.36.102003.152629.
38. Schlupp, I., Parzefall, J., and Schartl, M. 1991. Male mate choice in mixed bisexual/unisexual breeding complexes of Poecilia (Tele-ostei: Poeciliidae). Ethology, 88(3): 215-222. doi:10.1111/j.14390310.1991.tb00276.x.
39. Scott, W.B., and Crossman, E.J. 1979. Freshwater fishes of Canada. Bulletin of the Fisheries Research Board of Canada No. 184.
40. Vorburger, C. 2001. Fixation of deleterious mutations in clonal lineages: evidence from hybridogenetic frogs. Evolution, 55(11): 2319-2332. PMID:11794790.
41. Wilson, C.C., and Bernatchez, L. 1998. The ghost of hybrids past: fixation of arctic charr (Salvelinus alpinus) mitochondrial DNA in an introgressed population of lake trout (S. namaycush). Mol. Ecol. 7(1): 127-132. doi:10.1046/j.1365-294x.1998.00302.x.
42. Woodhead, A.D., and Armstrong, N. 1985. Aspects of the mating behavior of male mollies (Peocilia spp.). J. Fish Biol. 27(5): 593-601. doi:10.1111/j.1095-8649.1985.tb03204.x.