THE PALEOBOTANICAL RECORD OF COLOMBIA: IMPLICATIONS FOR BIOGEOGRAPHY AND BIODIVERSITY1

By H. Hooghiemstra, V. M. Wijninga, A. Cleef. 2006

197 citations recorded by the source corpus.

Subfields: Ecology, Ecology, Evolution, Behavior and Systematics, Food Science

View Paper: https://www.semanticscholar.org/paper/3c0bfcde3aadbc84964e8b06c94b7397c05fa8f7

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Citations in the corpus

Ecological implications of Cousinia Cass. (Asteraceae) persistence through the last two glacial–interglacial cycles in the continental Middle East for the Irano-Turanian flora (2012, background): “By contrast, in the northern Andes of Colombia, another example of low latitude mountain systems (~5°N), the highest vegetation belt kept nearly the same altitudinal extension as today during the LGM, i.e. between 2000 and 3000m (Hooghiemstra et al., 2006).”
Neotropical diversification seen through glassfrogs (2014, background): “7 Ma, corresponding to the most recent uplift of the Eastern Cordillera (Gregory-Wodzicki, 2000; Hooghiemstra et al., 2006).”
THE ANDES: A GEOLOGICAL OVERVIEW FROM A BIOLOGICAL PERSPECTIVE (2009, unknown): “The Bogotá Basin has been the site of important paleoenvironmental and vegetational history studies beginning with those of van der Hammen (e.g., van der Hammen et al., 1973) and continuing with those of Hooghiemstra (1984) and Hooghiemstra et al. (2006).”
Tropical and Temperate: Evolutionary History of Páramo Flora (2011, background): “Espeletia s.s., with the largest geographical range, occurs also in the Central and Western Colombian Cordilleras and in Ecuador (see, e.g., Hooghiemstra et al., 2006, Fig.”
The emerging field of geogenomics: Constraining geological problems with genetic data (2014, background): “O isotopes (Garzione et al., 2006; Ghosh et al., 2006; Leier et al., 2013), volcanic glass H isotopes (Saylor and Horton, 2014), and paleobotany (Gregory-Wodzicki, 2000; Hooghiemstra et al., 2006).”
Island biogeography of tropical alpine floras (2014, background): “…superp aramo of Sumapaz; although it is now surrounded by shrubby and grass p aramo, it was directly connected to other (super)p aramos of the Colombian Eastern Cordillera, such as Cocuy, during cold periods (van der Hammen & Cleef, 1986; Hooghiemstra et al., 2006; van der Hammen et al., 2008).”
Phylogenetic systematics of Glassfrogs (Amphibia: Centrolenidae) and their sister taxon Allophryne ruthveni (2009, background): “According to Hoorn (1995), the eastern cordillera formed a continuous range between 12.9 and 11.8 Ma; however, it probably became an important vicariant barrier to lowland species during the early Pliocene (5.3–3.6 Ma; Hooghiemstra et al., 2006).”
Evolutionary islands in the Andes: persistence and isolation explain high endemism in Andean dry tropical forests (2012, background): “…are likely to be less pronounced in the HEG biome, because the isolation of grasslands has varied over recent time due to the dramatic elevational shifts associated with the Pleistocene climatic fluctuations (van der Hammen & Cleef, 1986; Hooghiemstra & Cleef, 1995; Hooghiemstra et al., 2006).”
Mycorrhizas in changing ecosystems1,2 (2014, background): “) became prominent elements in the high-altitude Andean forests (Hooghiemstra et al. 2006).”