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Regional Species Richness (regional + species_richness)
Selected AbstractsPatterns of ant species richness along elevational gradients in an arid ecosystemGLOBAL ECOLOGY, Issue 2 2003Nathan J. Sanders ABSTRACT Aim In this study, we examine patterns of local and regional ant species richness along three elevational gradients in an arid ecosystem. In addition, we test the hypothesis that changes in ant species richness with elevation are related to elevation-dependent changes in climate and available area. Location Spring Mountains, Nevada, U.S.A. Methods We used pitfall traps placed at each 100-m elevational band in three canyons in the Spring Mountains. We compiled climate data from 68 nearby weather stations. We used multiple regression analysis to examine the effects of annual precipitation, average July precipitation, and maximum and minimum July temperature on ant species richness at each elevational band. Results We found that patterns of local ant species richness differed among the three gradients we sampled. Ant species richness increased linearly with elevation along two transects and peaked at mid-elevation along a third transect. This suggests that patterns of species richness based on data from single transects may not generalize to larger spatial scales. Cluster analysis of community similarity revealed a high-elevation species assemblage largely distinct from that of lower elevations. Major changes in the identity of ant species present along elevational gradients tended to coincide with changes in the dominant vegetation. Regional species richness, defined here as the total number of unique species within an elevational band in all three gradients combined, tended to increase with increasing elevation. Available area decreased with increasing elevation. Area was therefore correlated negatively with ant species richness and did not explain elevational patterns of ant species richness in the Spring Mountains. Mean July maximum and minimum temperature, July precipitation and annual precipitation combined to explain 80% of the variation in ant species richness. Main conclusions Our results suggest that in arid ecosystems, species richness for some taxa may be highest at high elevations, where lower temperatures and higher precipitation may support higher levels of primary production and cause lower levels of physiological stress. [source] Spatiotemporal changes of beetle communities across a tree diversity gradientDIVERSITY AND DISTRIBUTIONS, Issue 4 2009Stephanie Sobek Abstract Aim, Plant and arthropod diversity are often related, but data on the role of mature tree diversity on canopy insect communities are fragmentary. We compare species richness of canopy beetles across a tree diversity gradient ranging from mono-dominant beech to mixed stands within a deciduous forest, and analyse community composition changes across space and time. Location, Germany's largest exclusively deciduous forest, the Hainich National Park (Thuringia). Methods, We used flight interception traps to assess the beetle fauna of various tree species, and applied additive partitioning to examine spatiotemporal patterns of diversity. Results, Species richness of beetle communities increased across the tree diversity gradient from 99 to 181 species per forest stand. Intra- and interspecific spatial turnover among trees contributed more than temporal turnover among months to the total ,-beetle diversity of the sampled stands. However, due to parallel increases in the number of habitat generalists and the number of species in each feeding guild (herbivores, predators and fungivores), no proportional changes in community composition could be observed. If only beech trees were analysed across the gradient, patterns were similar but temporal (monthly) species turnover was higher compared to spatial turnover among trees and not related to tree diversity. Main conclusions, The changes in species richness and community composition across the gradient can be explained by habitat heterogeneity, which increased with the mix of tree species. We conclude that understanding temporal and spatial species turnover is the key to understanding biodiversity patterns. Mono-dominant beech stands are insufficient to conserve fully the regional species richness of the remaining semi-natural deciduous forest habitats in Central Europe, and analysing beech alone would have resulted in the misleading conclusion that temporal (monthly) turnover contributes more to beetle diversity than spatial turnover among different tree species or tree individuals. [source] Body size determines the strength of the latitudinal diversity gradientECOGRAPHY, Issue 3 2001Helmut Hillebrand In most groups of organisms, the species richness decreases from the tropics to the poles. The mechanisms causing this latitudinal diversity gradient are still controversial. We present data from a comprehensive weighted meta-analysis on the strength of the latitudinal gradient in relation to body size. We sampled literature data on the correlation between species richness and latitude for a variety of organisms, ranging from trees to protozoa. In addition, own data on the presence of large-scale diversity patterns for diatoms were included, both for local and regional species richness. The strength of the latitudinal gradient was positively correlated to the size of the organisms. Strongest decreases of species richness to the poles was found for large organisms like trees and vertebrates, whereas meiofauna, protozoa and diatoms showed weak or no correlations between species richness and latitude. These results imply that latitudinal gradients are shaped by non-equilibrium (regional) processes and are persistent under conditions of dispersal limitation. [source] The relationships between local and regional species richness and spatial turnoverGLOBAL ECOLOGY, Issue 5 2002Patricia Koleff Abstract Aim To determine the empirical relationships between species richness and spatial turnover in species composition across spatial scales. These have remained little explored despite the fact that such relationships are fundamental to understanding spatial diversity patterns. Location South-east Scotland. Methods Defining local species richness simply as the total number of species at a finer resolution than regional species richness and spatial turnover as turnover in species identity between any two or more areas, we determined the empirical relationships between all three, and the influence of spatial scale upon them, using data on breeding bird distributions. We estimated spatial turnover using a measure independent of species richness gradients, a fundamental feature which has been neglected in theoretical studies. Results Local species richness and spatial turnover exhibited a negative relationship, which became stronger as larger neighbourhood sizes were considered in estimating the latter. Spatial turnover and regional species richness did not show any significant relationship, suggesting that spatial species replacement occurs independently of the size of the regional species pool. Local and regional species richness only showed the expected positive relationship when the size of the local scale was relatively large in relation to the regional scale. Conclusions Explanations for the relationships between spatial turnover and local and regional species richness can be found in the spatial patterns of species commonality, gain and loss between areas. [source] Predicting the relationship between local and regional species richness from a patch occupancy dynamics modelJOURNAL OF ANIMAL ECOLOGY, Issue 2 2000B. Hugueny Summary 1.,A linear relationship between the number of species in ecological communities (local richness) and the species pools from which the communities are drawn (regional richness) suggests that species interactions are not sufficient to limit local richness and that communities are not saturated with species. Instead, this relationship implies that communities are open to regional influences and are interlinked by dispersal. 2.,Here we show how the linear relationship between local and regional richness in real, noninteractive, assemblages of cynipid gall wasps on California oaks, can be predicted from a simple patch-occupancy model. 3.,One cynipid assemblage has been surveyed for 3 years, allowing for crude estimates of colonization and extinction rates per patch. Using the mainland/island model of patch occupancy dynamics, these rates are combined with the observed number of cynipid species associated with each oak species (regional richness) to predict the expected local species richness in each patch. Assuming that species are independently distributed among localities, the expected variance in species richness among localities is also computed. 4.,The model is then tested on an independent data set. When differences in sampling effort (number of surveyed trees per locality) were accounted for, the regression equation relating observed (n = 41) to predicted local species richness does not differ statistically from the line of perfect agreement. The residuals are also distributed according to the predicted variance. 5.,Although not statistically significant, the variance in local richness appears to be slightly underestimated by the model. One explanation may be that cynipid species display some positive covariance in their distribution among localities, that is, groups of species occur together in given localities more frequently than would be expected by chance. Variance ratio tests identified statistically positive covariance within cynipid assemblages for three oaks species. 6.,The close fit of the model to the data supports the theoretical scenario for noninteractive communities, that the slope of the local,regional richness relationship and patch-occupancy processes are different expressions of the same phenomenon. [source] |