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Here we developed a composite pollen-based record of altitudinal vegetation changes from Lake Fúquene (5° N) in Colombia at 2540 m elevation. We quantitatively calibrated Arboreal Pollen percentages (AP%) into mean annual temperature (MAT) changes with an unprecedented ~60-year resolution over the past 284 000 years. An age model for the AP% record was constructed using frequency analysis in the depth domain and tuning of the distinct obliquity-related variations to the latest marine oxygen isotope stacked record. The reconstructed MAT record largely concurs with the ~100 and 41-kyr (obliquity) paced glacial cycles and is superimposed by extreme changes of up to 7 to 10° Celsius within a few hundred years at the major glacial terminations and during marine isotope stage 3, suggesting an unprecedented North Atlantic – equatorial link. Using intermediate complexity transient climate modelling experiments, we demonstrate that ice volume and greenhouse gasses are the major forcing agents causing the orbital-related MAT changes, while direct precession-induced insolation changes had no significant impact on the high mountain vegetation during the last two glacial cycles

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Colombian biomes are reconstructed at 45 sites from the modern period extending to the Last Glacial Maximum (LGM). The basis for our reconstruction is pollen data assigned to plant functional types and biomes at six 3000‐yr intervals. A reconstruction of modern biomes is used to check the treatment of the modern pollen data set against a map of potential vegetation. This allows the biomes reconstructed at past periods to be assessed relative to the modern situation. This process also provides a check on the a priori assignment of pollen taxa to plant functional types and biomes. For the majority of the sites, the pollen data accurately reflect the potential vegetation, even though much of the original vegetation has been transformed by agricultural practices. At 18 000 14C yr BP, a generally cool and dry environment is reflected in biome, assignments of cold mixed forests, cool evergreen forests and cool grassland–shrub; the latter extending to lower altitudes than presently recorded. This signal is strongly recorded at 15 000 and 12 000 14C yr BP, the vegetation at these times also reflecting a relatively cool and dry environment. At 9000 14C yr BP there is a shift to biomes thought to result from slightly cooler environmental conditions. This trend is reversed by 6000 14C yr BP; most sites, within a range of different environmental settings, recording a shift to more xeric biome types. There is an expansion of steppe and cool mixed‐forest biomes, replacing tropical dry forest and cool grassland–shrub biomes, respectively. These changes in biome assignments from the modern situation can be interpreted as a biotic response to mid‐Holocene climatic aridity. At 3000 14C yr BP the shift is mainly to biomes characteristic of slightly more mesic environmental conditions.There are a number of sites that do not change biome assignment relative to the modern reconstruction, although the affinities that these sites have to a specific biome do change. These ‘anomalies’ are interpreted on a site‐by‐site basis. Spatially constant, but differential response of the vegetation to climatic shifts are related to changes in moisture sources and the importance of edaphic controls on the vegetation. The Late Quaternary reconstruction of large‐scale vegetation dynamics in Colombia allows an understanding of the environmental controls on these to be developed. In particular, shifts in the character of the main climatic systems that influence Colombian vegetation are described. Copyright © 2002 John Wiley & Sons, Ltd.

Abstract. The biomisation method is used to reconstruct Latin American vegetation at 6000±500 and 18 000±1000 radiocarbon years before present (14C yr BP) from pollen data. Tests using modern pollen data from 381 samples derived from 287 locations broadly reproduce potential natural vegetation. The strong temperature gradient associated with the Andes is recorded by a transition from high altitude cool grass/shrubland and cool mixed forest to mid-altitude cool temperate rain forest, to tropical dry, seasonal and rain forest at low altitudes. Reconstructed biomes from a number of sites do not match the potential vegetation due to local factors such as human impact, methodological artefacts and mechanisms of pollen representivity of the parent vegetation. At 6000±500 14C yr BP 255 samples are analysed from 127 sites. Differences between the modern and the 6000±500 14C yr BP reconstruction are comparatively small; change relative to the modern reconstruction are mainly to biomes characteristic of drier climate in the north of the region with a slight more mesic shift in the south. Cool temperate rain forest remains dominant in western South America. In northwestern South America a number of sites record transitions from tropical seasonal forest to tropical dry forest and tropical rain forest to tropical seasonal forest. Sites in Central America show a change in biome assignment, but to more mesic vegetation, indicative of greater plant available moisture, e.g. on the Yucatán peninsula sites record warm evergreen forest, replacing tropical dry forest and warm mixed forest presently recorded. At 18 000±1000 14C yr BP 61 samples from 34 sites record vegetation reflecting a generally cool and dry environment. Cool grass/shrubland is prevalent in southeast Brazil whereas Amazonian sites record tropical dry forest, warm temperate rain forest and tropical seasonal forest. Southernmost South America is dominated by cool grass/shrubland, a single site retains cool temperate rain forest indicating that forest was present at some locations at the LGM. Some sites in Central Mexico and lowland Colombia remain unchanged in the biome assignments of warm mixed forest and tropical dry forest respectively, although the affinities that these sites have to different biomes do change between 18 000±1000 14C yr BP and present. The "unresponsive" nature of these sites results from their location and the impact of local edaphic influence.

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