The Historical Biogeography of Fagaceae: Tracking the Tertiary History of Temperate and Subtropical Forests of the Northern Hemisphere

By Paul S. Manos, Alice M. Stanford. INTERNATIONAL JOURNAL PLANT SCIENCES, 2001

291 citations recorded by the source corpus.

Subfields: Ecology, Evolution, Behavior and Systematics, Nature and Landscape Conservation, Plant Science

View Paper: https://www.semanticscholar.org/paper/4b3ff7dae197de3b698b18831f432f908bd29052

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Citations in the corpus

Phylogeography of the Southeast Asian stone oaks (Lithocarpus) (2003, methodology): “Comparative studies with lowland dominants, like the Dipterocarpaceae, or trees with different fruit dispersal syndromes, like the Myrtaceae, would also provide a complementary view to patterns emerging about the upland-dominant Fagaceae.”
Deterministic Plio‐Pleistocene extinctions in the European cool‐temperate tree flora (2003, unknown): “…appear to have been genetically isolated for 2–33 Myr with most divergences dating to the Miocene 5.3–23.8 Myr (Ricklefs & Latham 1992; Wen 1999; Manos & Stanford 2001), reflecting the Neogene disruption of the early to mid-Tertiary continuous Eurasian–North American temperate forest biome…”
History and Concepts of Big Plant Genera (2004, background): “(1999) and Manos & Stanford (2001) have fur- ished support for th hypothesis of Axelrod (1983) that, following an initial spread f ancestral stocks, the major groups of o ks essentially evolved and became established in the areas they now occupy.”
Forest aboveground biomass along an elevational transect in Sulawesi, Indonesia, and the role of Fagaceae in tropical montane rain forests (2010, background): “Thus specific ecological traits that favour adaptation to cool montane habitats, the long evolutionary history and probably the presence of the dipterocarps in the lowlands may have led to the unique importance in terms of AGB of this family in Southeast Asian compared with Neotropical montane fores”
Directional asymmetry of long‐distance dispersal and colonization could mislead reconstructions of biogeography (2005, methodology): “Fitch optimization (equally weighted parsimony) is a commonly used method (e.g. Enghoff, 1995; Andersson & Chase, 2001; Manos & Stanford, 2001; Lieberman, 2002) that, in effect, models dispersal and allopatric speciation (Ronquist, 2003).”
Community Assembly, Niche Conservatism, and Adaptive Evolution in Changing Environments (2003, background): “…spp. of North America and Europe exhibit virtually identical climatic response surfaces in their current distributions (Huntley et al. 1989), and they presumably diverged at least 15 Ma with the disruption of the North Atlantic Land Bridge (Manos and Stanford 2001; Tiffney and Manchester 2001).”
Phylogeny of Fagus L. (Fagaceae) based on morphological data (2003, background): “This is in conflict with two previous molecular based phylogenetic studies on Fagus (Stanford 1998, Manos and Stanford 2001) and will be discussed below.”
Consistent patterns of elevational change in tree taxonomic and phylogenetic diversity across Malesian mountain forests (2013, background): “…which are a central component of Malesian montane forests, have their centre of species radiation in Borneo, but the genera Castanopsis (D.Don) Spach and Lithocarpus evolved at least 40 Ma (Manos & Stanford, 2001; Cannon & Manos, 2003) and are distributed across Malesia today (Soepadmo, 1972).”
Chloroplast Phylogeny of Asplenioid Ferns based on rbcL and trnL-F Spacer Sequences (Polypodiidae, Aspleniaceae) and its Implications for Biogeography (2004, background): “…of several angiosperm groups that display disjunctions in their current distribution (Azuma et al. 2001; Donoghue et al. 2001; Fritsch et al. 2001; Lavin et al. 2001; Manos and Stanford 2001; Vinnersten and Bremer 2001; Xiang and Soltis 2001) including ‘‘Gondwana disjunctions’’ (Davis et al. 2002).”
The evolutionary history of Fagus in western Eurasia: Evidence from genes, morphology and the fossil record (2002, background): “Alice and Campbell 1999, Choi and Wen 2000, Hao et al. 2000, Manos 1997, Manos and Stanford 2001, Steane et al. 1999).”
A comprehensive framework for global patterns in biodiversity (2004, background): “For example, the diversity– environment relationship for plant clades that diversified in extratropical latitudes (e.g. Manos & Stanford 2001), including, by one estimate, more than 50 families of flowering plants (Ricklefs & Renner 1994), would differ substantially from that for flowering plants…”