Skip to main content

Genetic structure of the Far Eastern population of Eurasian wigeon Anas penelope inferred from sequencing of the mitochondrial DNA control region

We’re sorry, something doesn't seem to be working properly.

Please try refreshing the page. If that doesn't work, please contact support so we can address the problem.

Abstract

Sequence variation of the 5′ end of the mitochondrial DNA control region (600 bp) was examined in the population samples of Eurasian wigeon Anas penelope from Anadyr’ and Primorye. A total of 11 different mtDNA haplotypes were identified, with one of these belonging to American wigeon Anas americana. The presence of the mtDNA haplotype from the species closely relative to A. penelope in the Anadyr’ sample can be considered as the genetic evidence in favor of interspecific hybridization. This suggestion is in the good agreement with ornithological data. Genetic differentiation of the Primorye and Anadyr’ populations was low (Φst = 0.096). The phylogeographic structure was not pronounced.

This is a preview of subscription content, access via your institution.

References

  1. McCracken, K.G., Johnson, W.P., and Sheldon, F.H., Molecular Population Genetics, Phylogeography, and Conservation Biology of the Mottled Duck (Anas fulvigula), Cons. Genet., 2001, vol. 2, pp. 87–102.

    Article  CAS  Google Scholar 

  2. Kulikova, I.V., Drovetski, S.V., Gibson, D.D., et al., Phylogeography of the Mallard (Anas platyrhynchos): Hybridization, Dispersal and Lineage Sorting Contribute to Complex Geographic Structure, Auk, 2005, vol. 122, no. 3, pp. 949–965.

    Article  Google Scholar 

  3. Peters, J.L., McCracken, K.G., Zhuravlev, Y.N., et al., Phylogenetics of Wigeons and Allies (Anatidae: Anas): The Importance of Sampling Multiple Loci and Multiple Individuals, Mol. Phyl. Evol., 2005, vol. 35, pp. 209–224.

    Article  CAS  Google Scholar 

  4. Peters, J.L. and Omland, K.E., Population Structure and Mitochondrial Polyphyly in North American Gadwalls (Anas strepera), Auk, 2007, vol. 124, no. 2, pp. 444–462.

    Article  Google Scholar 

  5. Peters, J.L., Zhuravlev, Y., Fefelov, I., et al., Nuclear Loci and Coalescent Methods Support Ancient Hybridization as Cause of Mitochondrial Paraphyly between Gadwalls and Falcated Duck (Anas spp.), Evolution, 2007, vol. 61, no. 8, pp. 1992–2006.

    Article  CAS  PubMed  Google Scholar 

  6. Kulikova, I.V., Zhuravlev, Yu.N., and McCracken, K.G., Asymmetric Hybridization and Sex-Biased Gene Flow between Eastern Spot-Billed Ducks and Mallards in the Russian Far East, Auk, 2004, vol. 121, no. 3, pp. 930–949.

    Article  Google Scholar 

  7. Omland, K.E., Examining Two Standard Assumptions of Ancestral Reconstructions: Repeated Loss of Dichromatism in Dabbling Ducks (Anatini), Evolution, 1997, vol. 51, pp. 1636–1646.

    Article  Google Scholar 

  8. Johnsgard, P.A., Hybridization in the Anatidae and Its Taxonomic Implications, Condor, 1960, vol. 62, pp. 25–33.

    Article  Google Scholar 

  9. Greig, J.C., Duck Hybridization: A Threat to Species Integrity, Bokmakierie, 1980, vol. 32, pp. 88–89.

    Google Scholar 

  10. Cronin, M.A., Grand, J.B., Esler, D., et al., Breeding Populations of Northern Pintails Have Similar Mitochondrial DNA, Can. J. Zool., 1996, vol. 74, pp. 992–999.

    Article  Google Scholar 

  11. Isakov, Yu.A., Ptitsy Sovetskogo Soyuza (Birds of the Soviet Union), Moscow: Akad. Nauk SSSR, 1952, vol. 4, pp. 344–635.

    Google Scholar 

  12. Migratsii ptits Vostochnoi Evropy i Severnoi Azii: Plastinchatoklyuvye. Rechnye utki (Migrations of Birds of Eastern Europe and Northern Asia: Waterfowls. Anatids), Moscow: Nauka, 1997.

  13. Massey, J.A., Takano, S., and Sobone, K., A Field Guide to the Birds of Japan, Tokyo: Wild Bird Society of Japan, 1988.

    Google Scholar 

  14. Desjardins, P. and Morais, R., Sequence and Gene Organization of the Chicken Mitochondrial Genome: A Novel Gene Order in Higher Vertebrates, J. Mol. Biol., 1990, vol. 212, pp. 599–634.

    Article  CAS  PubMed  Google Scholar 

  15. Sorenson, M.D. and Fleischer, R.C., Multiple Independent Transpositions of Mitochondrial DNA Control Region Sequences to the Nucleus, Proc. Natl. Acad. Sci. USA, 1996, vol. 93, pp. 15239–15243.

    Article  CAS  PubMed  Google Scholar 

  16. Staden, R., Beal, K.F., and Bonfield, J.K., The Staden Package, 1998, Methods Mol. Biol., 2000, vol. 132, pp. 115–130.

    CAS  PubMed  Google Scholar 

  17. Tamura, K., Dudley, J., Nei, M., and Kumar, S., MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) Software Version 4.0, Mol. Biol. Evol., 2007, vol. 24, pp. 1596–1599.

    Article  CAS  PubMed  Google Scholar 

  18. Excoffier, L., Laval, G., and Schneider, S., Arlequin Ver. 3.0: An Integrated Software Package for Population Genetics Data Analysis, Evol. Bioinf. Online, 2005, vol. 1, pp. 47–50.

    CAS  Google Scholar 

  19. Swofford, D.L., Paup*: Phylogenetic Analysis Using Parsimony (*and Other Methods): Version 4.0b10, Sunderland: Sinauer Associates, 2002.

    Google Scholar 

  20. Clement, M., Posada, D., and Crandall, K.A., TCS: A Computer Program to Estimate Gene Genealogies, Mol. Ecol., 2000, vol. 9, p. 1657–1660.

    Article  CAS  PubMed  Google Scholar 

  21. Rogers, A.R. and Harpending, H., Population Growth Makes Waves in the Distribution of Pairwise Genetic Differences, Mol. Biol. Evol., 1992, vol. 9, pp. 552–569.

    CAS  PubMed  Google Scholar 

  22. Kuhner, M.K., Yamato, J., and Felsenstein, J., Maximum Likelihood Estimation of Population Growth Rates Based on the Coalescent Method, Genetics, 1998, vol. 149, pp. 429–434.

    CAS  PubMed  Google Scholar 

  23. Posada, D. and Crandall, K.A., Modeltest: Testing the Model of DNA Substitution, Bioinformatics, 1998, vol. 14, no. 9, pp. 817–818.

    Article  CAS  PubMed  Google Scholar 

  24. Harpending, H.C., Sherry, S.T., Rogers, A.R., and Stoneking, M., The Genetic Structure of Ancient Human Populations, Curr. Anthropol., 1993, vol. 34, pp. 483–496.

    Article  Google Scholar 

  25. Peters, J.L., Gretes, W., and Omland, K.E., Late Pleistocene Divergence between Eastern and Western Populations of Wood Ducks (Aix sponsa) Inferred by the ‘Isolation with Migration’ Coalescent Method, Mol. Ecol., 2005, vol. 14, pp. 3407–3418.

    Article  CAS  PubMed  Google Scholar 

  26. Avise, J.C., Alisauskas, R.T., Nelson, W.S., and Ankney, C.D., Matriarchal Population Genetic Structure in an Avian Species with Female Natal Philopatry, Evolution, 1992, vol. 46, no. 4, pp. 1084–1096.

    Article  Google Scholar 

  27. Krechmar, A.V. and Kondrat’ev, A.V., Plastinchatoklyuvye Ptitsy Severo-Vostoka Azii (Waterfowls of the Northeast of Asia), Anadyr’: SVNTs DVO RAN, 2006.

    Google Scholar 

  28. Nechaev, V.A. and Gorchakov, G.A., First Record of the Hybrid between Eurasian and American Wigeons (Anas penelope × A. americana) in Southern Primorye, Russ. Ornitolog. Zh., 1995, vol. 4, no. 1/2, pp. 68–69.

    Google Scholar 

  29. Kulikova, I.V. and Zhuravlev, Yu.N., Molecular Genetic Study of Anatid Interspecies Hybridization by Example of Mallard Anas platyrhynchos Superspecies Complex, Usp. Sovrem. Biol., 2009, vol. 129, no. 2, pp. 158–167.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to I. V. Kulikova.

Additional information

Original Russian Text © I.V. Kulikova, Yu.N. Zhuravlev, 2010, published in Genetika, 2010, Vol. 46, No. 8, pp. 1095–1101.

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Kulikova, I.V., Zhuravlev, Y.N. Genetic structure of the Far Eastern population of Eurasian wigeon Anas penelope inferred from sequencing of the mitochondrial DNA control region. Russ J Genet 46, 976–981 (2010). https://doi.org/10.1134/S1022795410080090

Download citation

  • Received:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S1022795410080090

Keywords

  • Eastern Population
  • Duck Species
  • Haplo Type
  • Central Haplotype
  • Mottled Duck