Imprints of glacial refugia in the modern genetic diversity of Pinus sylvestris

By R. Cheddadi, G. Vendramin, T. Litt, L. François, Masa Kageyama, Stephan Lorentz, J. Laurent, J. Beaulieu, L. Sadori, Anne Jost and 1 more. 2006

280 citations recorded by the source corpus.

Subfields: Atmospheric Science, Ecology, Evolution, Behavior and Systematics, Plant Science

View Paper: https://www.semanticscholar.org/paper/3130449682bdabed1abd67ce1cc16a96f80e6cce

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In Atmospheric Science

In Ecology, Evolution, Behavior and Systematics

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Citations in the corpus

Biogeography and evolution of Abies (Pinaceae) in the Mediterranean Basin: the roles of long‐term climatic change and glacial refugia (2011, unknown): “…play in allowing the persistence of relict species and the possibility of further migration in response to future climate change, as has happened repeatedly in the past, is subject to a number of uncertainties (Taberlet & Cheddadi, 2002; Terhürne-Berson et al., 2004; Cheddadi et al., 2006, 2009).”
Intra‐specific variability and plasticity influence potential tree species distributions under climate change (2011, background): “Intra-specific variation across populations has been demonstrated by genetic analysis of European tree populations (Petit et al., 2002; Cheddadi et al., 2006) mainly arising from the movement of populations since the last glaciation (Hewitt, 1999; Petit et al.”
Past tree range dynamics in the Iberian Peninsula inferred through phylogeography and palaeodistribution modelling: A review (2010, background): “Its range-wide population dynamics were subject to one of the first studies that combined palaeoecological and phylogeographical records with palaeodistribution modelling (Cheddadi et al., 2006).”
Geography determines genetic relationships between species of mountain pine (Pinus mugo complex) in western Europe (2010, background): “The latter has a shrubby (polycormic) growth habit and symmetrical cones, and forms large mats in subalpine habitats of the eastern Alps, the Erzgebirge, the Dinaric Alps, the Carpathians and the Rila and Pirin mountains of Bulgaria, with an isolated population in the Italian Apennines and other out”
Past and future range shifts and loss of diversity in dwarf willow (Salix herbacea L.) inferred from genetics, fossils and modelling (2009, background): “However, in two arctic-alpine buttercups, Ranunculus glacialis and R. pygmaeus , colonization of arctic areas may have been from the eastern Alps and the Urals, respectively, rather than from Central European lowland refugia, resulting in different genetic structures in these two species (Schönswett”
Ice age distributions of European small mammals: insights from species distribution modelling (2009, background): “If such models are then projected onto maps of LGM climatic conditions, the geographical distribution of suitable climatic conditions for the species during the LGM can be assessed (e.g. Cheddadi et al., 2006; Martı́nez-Meyer & Peterson, 2006; Carstens & Richards, 2007).”
Late Neogene history of the laurel tree (Laurus L., Lauraceae) based on phylogeographical analyses of Mediterranean and Macaronesian populations (2009, unknown): “Cheddadi et al., 2006), providing independent evidence that may help to reduce the uncertainty associated with the fossil record. Rodrı́guez-Sánchez & Arroyo (2008) used such a framework to reconstruct Laurus range dynamics over the past 3 Myr, documenting a process of range retreat and fragmentatio”
Historical climate modelling predicts patterns of current biodiversity in the Brazilian Atlantic forest (2008, background): “In the absence of extensive palaeontological data, spatial modelling of species or habitats under current and palaeoclimate regimes can generate hypotheses about the potential existence and extent of stable (refugial) areas, against which observations on species and genetic diversity, or from the fo”
Search for nucleotide diversity patterns of local adaptation in dehydrins and other cold-related candidate genes in Scots pine (Pinus sylvestris L.) (2008, background): “Northern areas of the present Scots pine distribution were covered by ice during last glacial maximum and colonized about 7,000–9,000 years ago from several refugia located in the Southern and Central Europe ( Cheddadi et al. 2006; Pyhajarvi et al. 2008; Soranzo et al. 2000).”
Applications of species distribution modeling to paleobiology (2011, background): “…for testing phylogeographic hypotheses (Knowles et al., 2007; Richards et al., 2007; Smith, 2007; Kozak et al., 2008) and applied in different ways in an increasing number of studies (Cheddadi et al., 2006; Carstens and Richards, 2007; Knowles et al., 2007; Waltari et al., 2007; Vega et al., 2010).”
Potential for evolutionary responses to climate change – evidence from tree populations (2013, background): “…species by combining phylogeographic and palynological approaches with coalescent-based studies of population demography (Petit et al., 2002; McLachlan et al., 2005; Cheddadi et al., 2006; Heuertz et al., 2006; Magri et al., 2006; Soltis et al., 2006; Eckert et al., 2010; Parducci et al., 2012).”
Colonization routes of Pinus sylvestris inferred from distribution of mitochondrial DNA variation (2008, background): “Based on genetic data, it is highly probable that there were some isolated populations in the Iberian and Italian Peninsulas during the LGM (Sinclair et al. 1999; Soranzo et al. 2000; Cheddadi et al. 2006).”
Genetic structure of Hypochaeris uniflora (Asteraceae) suggests vicariance in the Carpathians and rapid post‐glacial colonization of the Alps from an eastern Alpine refugium (2007, background): “In the light of these fossil records, we cannot exclude the possibility that some coniferous forests survived the Last Glacial stage (Würm) in the Skhidni Beskidi Mountains (Ravazzi, 2002; Cheddadi et al., 2006), thus separating alpine and subalpine vegetation zones of the western and eastern Carpat”