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Dating in Webster. Dating in Wembley. Dating in Wesley Creek. Dating in Westlock. Lineage C may not have successfully recolonised the northern parts of eastern Europe Poland north of the Carpathians, Belarus and Lithuania but, as suggested by our Russian sample, became confined to the east of the distribution range of lineage A.

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This is in line with the fact that the proportion of C haplotypes increases towards the south and the east. However, since we are dealing with red deer, arguably the most important and most highly held European game species, translocations are the crucial unknown entering the equation.

These translocations may have contributed to high genetic diversity in some areas through the introduction of divergent haplotypes. This may particularly hold for western Germany with the aberrant haplotype The very high nucleotide diversity found in eastern Belarus is due to the presence of both most divergent haplotypes from the C lineage 9 and 15but whether this is due to translocations or natural migration remains unclear.

Haplotype 1 is found in eastern Germany and particularly north-eastern Poland, haplotype 20 in eastern Germany and Lithuania, and an even more disjunct distribution is shown by haplotypes 2, 8 and 10 which are found in western Germany and Poland including the northeast of the country. However, the most unlikely candidate for a natural distribution is haplotype 4: it is found in western Germany and then again in northeastern Poland, Belarus and Lithuania.

Such a pattern is almost certainly a result of translocations. There are several documented records of translocations of red deer at the end of the nineteenth and beginning of the twentieth centuries from Germany to north-eastern Poland, e. After the translocations, the number of red deer in north-eastern Poland increased, and in the twentieth century they were translocated or migrated to neighbouring countries, e.

This might be an explanation for the presence of haplotype 2 in only Germany and western and north-eastern Poland. The distribution of haplotypes 8 and 10 could also be the result of human impacts; alternatively, these haplotypes may be widespread in Poland through natural migration.

Why not tell all your lesbian and bi female friends that we run Only Women just for them? Juan @CA-Juan is a 43 year old Bisexual Male from Calgary, Alberta, Canada. Find Personals listings in Milwaukee on Oodle Classifieds. Join millions of people using Oodle to find great personal ads. Don't miss what's happening in your neighborhood. Ultimately, only ancient DNA analyses of red deer remains or trophies dating back to before translocations were carried out (ideally early or middle Holocene samples), perhaps combined with detailed local population genetic analyses and admixture studies, can answer the question if the present domination of western haplotypes in northeastern Cited by:

Since obviously on this geographical scale human management has blurred the natural genetic structure of red deer in eastern Europe, it is impossible to fully disentangle natural and anthropogenic patterns. Interestingly, though, the amount of mismatch between genetic lineages and geography is much higher in our study area than in the rest of Europe where Skog et al.

This may suggest that inter-lineage translocations were more common in eastern Europe, or alternatively, it may simply be the result of the two lineages occurring parapatrically in the east which will make admixture more likely if translocations are carried out or natural migration occurs. Ultimately, only ancient DNA analyses of red deer remains or trophies dating back to before translocations were carried out ideally early or middle Holocene samplesperhaps combined with detailed local population genetic analyses and admixture studies, can answer the question if the present domination of western haplotypes in northeastern Europe is natural or caused by human interference.

We are grateful to Barbara Marczuk for her help with the laboratory work. This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author s and source are credited. Maximum parsimony tree of the 69 red deer mtDNA control region haplotypes found in the present study.

All three lineages form monophyletic clades, albeit with low bootstrap support numbers at brans give percentage values based on 1, replicates. The two encircled haplotypes are the one from Mesola 41 and the aberrant one found in western Germany National Center for Biotechnology InformationU. Acta Theriologica. Acta Theriol Warsz. Published online Nov Hartl2 Tomasz Borowik1 Aleksei N.

Bunevich7 Johannes Lang8 and Frank E. Zachos 1, 2. Vadim E. Aleksei N. Frank E. Author information Article notes Copyright and License information Disclaimer.

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Zachos, Email: ed. Corresponding author. Received Jun 30; Accepted Oct 8. This article has been cited by other articles in PMC. Introduction The cyclic climatic changes during the Quaternary have had a profound impact on the genetic structure of European temperate species in that these have been undergoing repeated range contractions and expansions in the wake of glacial and interglacial pulses e.

Material and methods Sampling information Muscle or skin samples from legally culled red deer were collected in Denmark, Germany, Poland, Belarus, Ukraine, Lithuania and Russia see Fig. Open in a separate window. Haplotype Frequency Nomenclature according to Skog et al. Czech R. Czech Republic, L lowland, C Carpathian a Haplotype 16 is the divergent sequence found in western Germany which is not easily assignable to any of the three lineages. Discussion We analysed mitochondrial control region sequences from almost 1, red deer sampled throughout their entire European distribution range.

Open Access This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author s and source are credited. Appendix Maximum parsimony tree of the 69 red deer mtDNA control region haplotypes found in the present study. Brown hares on the edge: genetic population structure of the Danish brown hares.

Acta Theriol. Median-joining networks for inferring intrcific phylogenies. Mol Biol Evol. Trudy VGZ, Voronezh, vol. Proceedings of the Royal Society London B - doi Heredity - doi Rominten-Gestern und Heute. Bothel: Nimrod-Verlag; Phylogeography and founder effect of the endangered Corsican red deer Cervus elaphus corsicanus Biodivers Conserv.

Nucleic Acids Symp Ser. Comptes Rendus Biologies SS42 doi Some genetic consequences of ice ages, and their role in divergence and speciation.

Biol J Linn Soc. Post-glacial recolonization of European biota. The genetic legacy of the Quaternary ice ages. Conservation genetics of the endangered red deer from Sardinia and Mesola with further remarks on the phylogeography of Cervus elaphus corsicanus. Biol J Linn Soc - doi Genetic variability and differentiation in red deer Cervus elaphus from Scotland and England.

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Biol J Zool. Ee istoriskii ork, sovremennoe okhotni khozaistvo i vysochaishe okhoty v Push.

Genetic diversity, gene flow and drift in Bavarian red deer populations Cervus elaphus Conserv Genet. Genetic roots of the red deer Cervus elaphus population in Eastern Switzerland. J Heredity. Wildbahn und Jagd Altpreussens im Wandel der geschichtlin Jahrhunderte. Neumann, Neudamm und Berlin: Verlag J; Der Wald in Altpreussen als Wirtschaftsraum.

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Ungulates and their management in Romania. European Ungulates and their Management in the 21st Century. Cambridge: Cambridge University Press; Genetic variation and population structure of the Japanese sika deer Cervus nippon in Hokkaido Island, based on mitochondria D-loop sequences.

Mol Ecol. Hamburg, Berlin: Paul Parey; Population genetic structure of wild boar Sus scrofa in Bulgaria as revealed by microsatellite analysis. Genetic consequences of human management in an introduced island population of red deer Cervus elaphus Heredity. Ecological factors influence population genetic structure of European Grey wolves. Molecular Ecology.

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Modeltest: testing the model of DNA substitution. Intrcific gene genealogies: trees grafting into networks. Trends Ecol Evol. Bioinformatics - doi Phylogeography of red deer Cervus elaphus in Europe.

J Biogeogr. Glacial refugia of mammals in Europe: evidence from fossil records. Mamm Rev. Late Quaternary distribution dynamics and phylogeography of the red deer Cervus elaphus in Europe.

Quat Sci Rev. Druk Gazety Rolniczej W. Comparative phylogeography and postglacial colonization routes in Europe. Mol Biol Evol - doi FaBox: an online toolbox for fasta sequences. Molecular Ecology Notes. Genetic analysis of an isolated red deer Cervus elaphus population showing signs of inbreeding depression.

European Journal of Wildlife Research. Population viability analysis and genetic diversity of the endangered red deer population from Mesola, Italy. Wildlife Biol. On the phylogeographic origin of the Corsican red deer Cervus elaphus corsicanus : evidence from microsatellites and mitochondrial DNA. Mamm biol.

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