Chloroplast DNA variation in European white oaks phylogeography and patterns of diversity based on data from over 2600 populations

By R. J. Petita, Ulrike M. Csaiklb, Sándor Bordácsb, Kornel Burgb, E. Coartd, Joan Cottrelle, Barbara van Damf, John D. Deansg, Sylvie Dumolin-Lapèguea, Silvia Fineschih and 19 more. 2002

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Subfields: Cell Biology, Genetics, Molecular Biology

View Paper: https://www.semanticscholar.org/paper/e18d9d3df17f294a8aff23d60547f516e73c1870

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Citations in the corpus

Macroecological patterns of species and genetic diversity in vascular plants of the Mediterranean basin (2010, background): “…Mediterranean climate, probably derive from Mediterranean Pleistocene refugia (A. alba, Liepelt et al., 2009; 60 Diversity and Distributions, 16, 53–64, ª 2009 Blackwell Publishing Ltd Corylus avelana, Palme & Vendramin, 2002; Fagus sylvatica, Magri et al., 2006; Quercus sp., Petit et al., 2002).”
Phylogeographical structure and conservation genetics of wild grapevine (2006, methodology): “…the genome, HD ¼ Xr j¼1 hj=r Geographic trends were investigated by computing diversity (HD) and differentiation statistics (HT, HS, and GST) calculated following Pons and Petit (1996) and Petit et al. (2002) for three groups of populations: Iberian peninsula, Italian peninsula and Caucasus region.”
Phylogeography of the Southeast Asian stone oaks (Lithocarpus) (2003, methodology): “The species independence of cpDNA markers in this study and others (Golden & Bain, 2000; Petit et al., 2002) should provide a cautionary tale for phylogeographical studies of cytoplasmic markers, particularly when species boundaries are poorly understood.”
Genetic homogeneity in Juglans nigra (Juglandaceae) at nuclear microsatellites (2006, background): “…vast majority of DNA-level studies to date have employed chloroplast or mitochondrial DNA markers (e.g., Mitton et al., 2000; Liepelt et al., 2002; Petit et al., 2002, 2003; Magni et al., 2005); however, nuclear markers can also contribute to our understanding of postglacial range expansion and…”
Comparative phylogeography of unglaciated eastern North America (2006, methodology): “Subsequent postglacial population expansion across restricted mountain passes resulted in congruent phylogeographical structure among many diverse taxa (Hewitt 1999; Petit et al. 2002).”
Comparative phylogeography and population structure of European Betula species, with particular focus on B. pendula and B. pubescens (2007, background): “Third, with a few exceptions (e.g. Petit et al., 2002, 2003a; Heuertz et al., 2006a), most studies have focused on a single species, ignoring the fact that a large number of plant species exhibit a very high level of hybridization and introgression [for example within Quercus (Dumolin-Lapègue et…”
Global patterns of genetic variation in plant species along vertical and horizontal gradients on mountains (2008, background): “Similarly, areas where refugia have been postulated, such as the Iberian and Italian peninsulas, generally displayed higher levels of chloroplast diversity in oak (Quercus) species (Petit et al., 2002).”
Patterns and dynamics of European vegetation change over the last 15,000 years (2017, background): “Genetic markers in Quercus document that many populations from around the Mediterranean Basin have spread north with post-glacial warming (Petit et al., 2002), yet these immigration routes find no reflection in a differentiated time of initial population expansion (Brewer et al., 2002; Giesecke,…”
Assessment of the Genetic Diversity in Forest Tree Populations Using Molecular Markers (2014, background): “diagnostic markers [33–35], dependent on the evidence of their maternal inheritance in the species, were used to trace back the colonization history of angiosperm forest tree species and conifers, respectively [36,37].”
Detecting interspecific and geographic differentiation patterns in two interfertile oak species (Quercus petraea (Matt.) Liebl. and Q. robur L.) using small sets of microsatellite markers. (2010, background): “This supports historical introgressive hybridization, 22 which has led to frequent cytoplasmic exchanges through pollen swamping (Petit et 23 al., 1997; Petit et al., 2002).”