Palm species distributions |
Topography, drainage, vegetation |
All 23 palm species in a 50 ha plot |
South America |
Local |
Palm species distributions were related to microhabitat variables, mainly topography, but also drainage and canopy height. |
Svenning (1999) |
Soil, human influence |
Seven species of canopy and sub-canopy palms |
Central America |
Local–landscape |
Distribution and abundance of five palm species is related to edaphic variation. The distribution of one species is influenced by human harvesting. |
Clark et al. (1995) |
Temperature, topography |
Euterpe edulis |
South America |
Landscape |
The distribution of E. edulis is constrained by low temperatures and possibly dew formation (especially occurring in valleys). |
Gatti et al. (2008) |
Climate |
Trachycarpus fortunei |
Europe, Asia |
Regional–continental |
There is a strong relationship between minimum winter temperatures (influenced by growing season length) and the native and invasive distribution of this palm. |
Walther et al. (2007) |
Climate, soil, habitat, human impact, space |
29 palm species |
Africa |
Continental |
Climate (especially water availability) and space (possibly reflecting dispersal limitation) are the most important distributional determinants for most palm species. Soil type is only relevant for a few dry-climate species, possibly reflecting hydrology. |
Blach-Overgaard et al. (2010) |
Topography, species traits |
62 palm species |
South America |
Local/landscape–continental |
Palm species abundance at the landscape scale was related to topographic niche breadth, while continental range size correlated with stem height (possibly reflecting species' dispersal potential). |
Kristiansen et al. (2009) |
Palm community composition |
Soil fertility and texture, topography, spatial distance |
All palms; non-inundated lowland rainforest |
South America |
Local |
Palm community composition is related to soil fertility (cations), texture (sand content), elevation and spatial distance. The environmental predictors remain important when spatial distance is taken into account, but not vice versa. |
Poulsen et al. (2006) |
Hydrology, topography, canopy openness, spatial distance |
All palms; forest on palaeo-riverine terraces |
South America |
Local–landscape |
At local scale, most variation (approx. 85 %) remains unexplained, with soil moisture being the strongest predictor. At the landscape scale, geographic distance explains most variation (88 %), and composition exhibits links to larger-scale biogeographic patterns (e.g. species with sub-Andean affinities in western local assemblages). |
Normand et al. (2006) |
Soil, precipitation, vegetation, spatial distance |
Understorey palms; lower montane forest |
Central America |
Landscape |
Variation in palm community similarity is related to soil properties (especially inorganic nitrogen availability and cation concentration), but also climate and geographic distance. |
Andersen et al. (2010) |
Soil fertility and texture, hydrology, topography, spatial distance |
All palms; non-inundated lowland rainforest |
South America |
Landscape |
Palm community composition is strongly related to soil clay content and for a sub-set (understorey palms in bottomlands) also to distance to watercourses. Soil fertility, topography (slope) and spatial distance were not relevant predictors. |
Costa et al. (2009) |
Topography, space |
All palms; montane rainforest |
South America |
Local–landscape |
Both topography and spatial location imposed strong controls on palm community composition. |
Svenning et al. (2009) |
Soil, topography, spatial distance |
All palms; non-inundated lowland rainforest |
South America |
Landscape–regional |
Palm community composition is more strongly related to geographic distance than to environmental variables. Soil fertility and texture are the only relevant environmental factors. |
Vormisto et al. (2004a) |
Geographic distance, climate, topography, vegetation, soil |
All New World palms |
Americas |
Continental |
Geographic distance decay in palm community similarity depends more on geographic distance than on environmental distance. Environmentally complex or geographically fragmented sub-regions exhibit stronger distance decays than more homogenous sub-regions. |
Bjorholm et al. (2008) |
Palm species richness |
Area, mid-domain effect |
All palms in New Guinea |
Australasia |
Regional |
Area and a mid-domain effect explain the majority of variation in palm species richness along an elevational gradient. |
Bachman et al. (2004) |
Climate, topography, vegetation, space |
All New World palms |
Americas |
Continental |
Water-related variables (annual rainfall, number of wet days) are the most important environmental predictors for palm species richness, followed by soil fertility. Space (latitude squared) is the dominant spatial variable. |
Bjorholm et al. (2005, 2006) |
Climate, topography |
All New World palms |
Americas |
Continental |
Climatic factors related to energy and water availability and productivity determine the species richness of widespread palms, but the species richness of range-restricted palms is to some extent determined by topographical complexity, too. |
Kreft et al. (2006) |
Climate |
All Brazilian palms |
South America |
Continental |
Water availability and temperature seasonality are most important in determining palm species richness. |
Salm et al. (2007) |
Climate, topography, net diversification rate |
All New World palms |
Americas |
Continental |
Palm species richness increases with net diversification at both deep and shallow phylogenetic levels, and all increase with decreasing (absolute) latitude and increasing energy/temperature and water availability. An increase of species richness with topographic range is linked to recent diversification. |
Svenning et al. (2008) |