A new scenario for the quaternary history of European beech populations: palaeobotanical evidence and genetic consequences.

By D. Magri, G. Vendramin, B. Comps, Isabelle Dupanloup, T. Geburek, D. Gömöry, M. Latałowa, T. Litt, L. Paule, J. Roure and 4 more. New Phytologist, 2006

920 citations recorded by the source corpus.

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

View Paper: https://www.semanticscholar.org/paper/64f4ee72032ce270adf655af870142da936daa6c

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Citations in the corpus

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).”
Global patterns of genetic variation in plant species along vertical and horizontal gradients on mountains (2008, background): “In such cases, ridges may provide important habitats and pathways, as reported by Magri et al. (2006). Species thus affected need to be conserved immediately.”
Biological Flora of the British Isles: Fagus sylvatica (2012, methodology): “In northern Europe (Denmark, southern Norway, southern Sweden), Fagus sylvatica in leaf is very vulnerable to gales, and old unmanaged beech forests that have been left to grow naturally contain trees of many different ages. Very many of the trees involved developed from shade-tolerant dwarf trees t”
Patterns and dynamics of European vegetation change over the last 15,000 years (2017, background): “However, we found that Fagus populations on the Balkan and Iberian Peninsulas remained small until the mid-Holocene and grew in parallel with the populations in central Europe (Fig.”
Phylogeographic insights into cryptic glacial refugia. (2008, background): “Likewise, the combined analysis of palaeontological and genetic data [65], rather than carrying out genetic analysis and then referring to fossil records for a posteriori explanations, can provide novel information on refugial survival and postglacial recolonisation, such as further evidence for a c”
Comparative phylogeography and population structure of European Betula species, with particular focus on B. pendula and B. pubescens (2007, background): “More generally, the results in birch, together with recent results in beech (Magri et al., 2006) and Norway spruce (Heuertz et al., 2006b), should lead to a reassessment of ‘a priori’ models of recolonization in forest trees.”
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).”
Disturbance refugia within mosaics of forest fire, drought, and insect outbreaks (2020, background): “Long- term micro/macrorefugia have been identified using fossil evidence (Magri et al. 2006) and examined via dendrochronology (Holz et al. 2018), which facilitate the reconstruction of past climate- change–vegetation relationships over longer time scales.”
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): “…as a glacial refugium has also been revealed by molecular and palaeofossil studies on temperate trees (King & Ferris, 1998; Petit et al., 2002; Magri et al., 2006), butterflies (Schmitt & Seitz, 2001), amphibians (Babik et al., 2005), snakes (Ursenbacher et al., 2006) and mammals (Jaarola &…”
Direct evidence of central European forest refugia during the last glacial period based on mollusc fossils (2014, background): “Though some direct evidence exists for pollen and plant remains (e.g., Birks, 2003; Magri et al., 2006; Jankovská and Pokorný, 2008), snails (Ložek, 2006) and mammals (e.”
Quantifying phenological plasticity to temperature in two temperate tree species (2010, background): “Indeed, pollen records, chloroplast DNA analyses (Brewer et al. 2002; Petit et al. 2002; Magri et al. 2006) and field observations (Walther et al. 2002) demonstrate that species migration is highly correlated with global climatic cycles.”
Bioclimatology of beech (Fagus sylvatica L.) in the Eastern Alps: spatial and altitudinal climatic signals identified through a tree‐ring network (2007, background): “Journal compilation ª 2007 Blackwell Publishing Ltd Genetic research has shown a different origin of the Apennine and Alpine beech populations (Vettori et al., 2004; Magri et al., 2006).”
Seed dispersal distances: a typology based on dispersal modes and plant traits (2007, background): “However, as was recently found forFagus sylvatica (Magri et al. 2006), it is possible that those recolonisation rates are overestimated because some glacial refugia remain yet unknown (Clark et al. 1998; Stewart and Lister 2001; Pearson 2006).”
What do we mean by 'refugia'? (2008, background): “European beech (Fagus sylvatica) has generally been scarce during interglacials and glacials alike, but was abundant in the stadials at the beginning of the last glacial, and has become abundant during the late Holocene (Magri et al., 2006).”