68 research outputs found

    Do Rapoport's Rule, Mid-Domain Effect or Environmental Factors Predict Latitudinal Range Size Patterns of Terrestrial Mammals in China?

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    BACKGROUND: Explaining species range size pattern is a central issue in biogeography and macroecology. Although several hypotheses have been proposed, the causes and processes underlying range size patterns are still not clearly understood. In this study, we documented the latitudinal mean range size patterns of terrestrial mammals in China, and evaluated whether that pattern conformed to the predictions of the Rapoport's rule several analytical methods. We also assessed the influence of the mid-domain effect (MDE) and environmental factors on the documented range size gradient. METHODOLOGY/PRINCIPAL FINDINGS: Distributions of 515 terrestrial mammals and data on nine environmental variables were compiled. We calculated mean range size of the species in each 5° latitudinal band, and created a range size map on a 100 km×100 km quadrat system. We evaluated Rapoport's rule according to Steven's, mid-point, Pagel's and cross-species methods. The effect of the MDE was tested based on a Monte Carlo simulation and linear regression. We used stepwise generalized linear models and correlation analyses to detect the impacts of mean climate condition, climate variability, ambient energy and topography on range size. The results of the Steven's, Pagel's and cross-species methods supported Rapoport's rule, whereas the mid-point method resulted in a hump-shaped pattern. Our range size map showed that larger mean latitudinal extents emerged in the mid-latitudes. We found that the MDE explained 80.2% of the range size variation, whereas, environmental factors accounted for <30% of that variation. CONCLUSIONS/SIGNIFICANCE: Latitudinal range size pattern of terrestrial mammals in China supported Rapoport's rule, though the extent of that support was strongly influenced by methodology. The critical factor underlying the observed gradient was the MDE, and the effects of climate, energy and topography were limited. The mean climate condition hypothesis, climate variability hypothesis, ambient energy hypotheses and topographical heterogeneity hypotheses were not supported

    Elevational Gradients in Bird Diversity in the Eastern Himalaya: An Evaluation of Distribution Patterns and Their Underlying Mechanisms

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    BACKGROUND: Understanding diversity patterns and the mechanisms underlying those patterns along elevational gradients is critically important for conservation efforts in montane ecosystems, especially those that are biodiversity hotspots. Despite recent advances, consensus on the underlying causes, or even the relative influence of a suite of factors on elevational diversity patterns has remained elusive. METHODS AND PRINCIPAL FINDINGS: We examined patterns of species richness, density and range size distribution of birds, and the suite of biotic and abiotic factors (primary productivity, habitat variables, climatic factors and geometric constraints) that governs diversity along a 4500-m elevational gradient in the Eastern Himalayan region, a biodiversity hotspot within the world's tallest mountains. We used point count methods for sampling birds and quadrats for estimating vegetation at 22 sites along the elevational gradient. We found that species richness increased to approximately 2000 m, then declined. We found no evidence that geometric constraints influenced this pattern, whereas actual evapotranspiration (a surrogate for primary productivity) and various habitat variables (plant species richness, shrub density and basal area of trees) accounted for most of the variation in bird species richness. We also observed that ranges of most bird species were narrow along the elevation gradient. We find little evidence to support Rapoport's rule for the birds of Sikkim region of the Himalaya. CONCLUSIONS AND SIGNIFICANCE: This study in the Eastern Himalaya indicates that species richness of birds is highest at intermediate elevations along one of the most extensive elevational gradients ever examined. Additionally, primary productivity and factors associated with habitat accounted for most of the variation in avian species richness. The diversity peak at intermediate elevations and the narrow elevational ranges of most species suggest important conservation implications: not only should mid-elevation areas be conserved, but the entire gradient requires equal conservation attention

    Species Diversity and Life-Form Patterns in Steppe Vegetation along a 3000 m Altitudinal Gradient in the Alborz Mountains, Iran

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    <p>Biodiversity pattern and life-form spectra were studied along a 3,000 m altitudinal gradient from a semi-desert area to the alpine peak of Tochal Mountain. The gradient is located on the southern slopes of Central Alborz with a Mediterranean continental climate. DCA ordination was applied to 1,069 relev,s and 7 quantitative variables to discover the relation of diversity and altitude. A biodiversity pattern was obtained by relating values for species richness and Shannon-Wiener's index to 100-m altitudinal sections. Altitude was determined as the major ecological gradient. Both diversity indices are negatively correlated with altitude and show a decreasing trend beyond a peak in species richness at 1,800-1,900 m a.s.l. towards a very low diversity in the high alpine zone. The biodiversity peak does not match with the potential tree line in the area (2,500-3,000 m a.s.l.). The high diversity in foothills can be related to habitat heterogeneity, longer suitable climatic conditions, and diverse disturbance factors, while unfavorable conditions at high-altitude alpine and low-altitude desert areas reduce the number of species at both extremes. Life-form patterns clearly change along altitudinal gradient. Annuals with decreasing trend, and hemicryptophytes and chamaephytes with increasing trend along the altitudinal gradient are notable patterns of life form in the area. Temperature, soil moisture and nutrients are the main factors that explain the ecological influence of altitude on species diversity and life-form patterns in the semi-arid steppe vegetation of the area.</p>

    Subalpine-nival gradient of species richness for vascular plants, lichens and bryophytes in the Swiss Inner Alps

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    In the European GLORIA project, 12 summits (treeline to nival belt) were inventoried in three regions of Switzerland: two in the Swiss National Park Graubünden and one in Valais. Vascular plants were recorded in all three regions and bryophytes and lichens were recorded only in Valais. On each summit, vegetation and temperature data were sampled using sampling protocols for the GLORIA project (Global Observation Research Initiative in Alpine environment) on large summit sections and in clusters of four 1x1-m quadrats. We observed a general decrease of species richness for all three systematic groups with increasing elevation in the summit sections, but only for vascular plants in the quadrats. In Valais, there was higher species richness for vascular plants than for bryophytes and lichens on the lower summits, but as the decrease in species richness was less pronounced for cryptogams, the latter were more numerous than vascular plants on the highest summit. Vascular species showed a clear shift of the dominant life form with elevation, with chamaephytes replacing hemicryptophytes. Bryophytes and lichens showed a weak trend among the life forms at the summit section scale, but a stronger shift of the dominant forms was seen in the quadrats, with cushion replacing turf bryophytes and crustaceous replacing fruticose lichens. Altogether, these results sustain the temperature-physiographic hypothesis to explain the species richness decrease along the altitudinal gradient: the harsh climatic conditions of the alpine-nival belts act as a filter for species, but the diminishing diversity of microhabitats is also an important factor. Because cryptogams depend more on humidity than temperature and more on smaller microhabitats than vascular plants, the decrease of species richness is more gradual with elevation for bryophytes and lichens

    Elevational patterns of species richness and density of rattan palms (Arecaceae: Calamoideae) in Central Sulawesi, Indonesia

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    We studied species richness and density of rattan palms in 50 plots of 10 × 100 m2 each between 250 m and 2420 m in eight sites in Lore Lindu National Park (LLNP), Central Sulawesi. Rattans were observed in all sample sites, representing three genera and 34 species. The elevational patterns for species richness and density were humped-shaped with maxima around 1000 m. Polynomial models of second order explained 59 and 32% of species richness and density with the factor elevation, respectively. A majority of rattan species (65%) overlapped between 1000 and 1100 m elevation, while a pronounced change in the rattan flora occurred above 1100 m. Commercially important rattan species (Calamus zollingeri, C. ornatus var. celebicus, Daemonorops macroptera) were not observed above 1250 m. The change of species assemblage was significantly related to elevation (56%), followed by geographical distance (47%) and precipitation (40%). Less than 10% of LLNP is lowland forests, much of which is threatened by agricultural intensification. In contrast, montane forests are well represented in the park and high elevation forests are not subject to agricultural conversion or intensive harvesting of rattan and other forest products

    Cross-scale analysis of the region effect on vascular plant species diversity in southern and northern European mountain ranges.

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    Background: The divergent glacial histories of southern and northern Europe affect present-day species diversity at coarse-grained scales in these two regions, but do these effects also penetrate to the more fine-grained scales of local communities?Methodology/Principal Findings: We carried out a cross-scale analysis to address this question for vascular plants in two mountain regions, the Alps in southern Europe and the Scandes in northern Europe, using environmentally paired vegetation plots in the two regions (n = 403 in each region) to quantify four diversity components: (i) total number of species occurring in a region (total gamma-diversity), (ii) number of species that could occur in a target plot after environmental filtering (habitat-specific gamma-diversity), (iii) pair-wise species compositional turnover between plots (plot-to-plot beta-diversity) and (iv) number of species present per plot (plot gamma-diversity). We found strong region effects on total gamma-diversity, habitat-specific gamma-diversity and plot-to-plot beta-diversity, with a greater diversity in the Alps even towards distances smaller than 50 m between plots. In contrast, there was a slightly greater plot alpha-diversity in the Scandes, but with a tendency towards contrasting region effects on high and low soil-acidity plots.Conclusions/Significance: We conclude that there are strong regional differences between coarse-grained (landscape- to regional-scale) diversity components of the flora in the Alps and the Scandes mountain ranges,but that these differences do not necessarily penetrate to the finest-grained (plot-scale) diversity component, at least not on acidic soils. Because different processes can lead to a similar pattern, we discuss the consistency of our results with Quaternary history and other divergent features between the two regions such as habitat connectivity, selection for vagility and environmental differences not accounted for in our analyse
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