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1.
物种多样性海拔分布格局及其形成机制的研究是生物地理学和宏观生态学的重要议题之一。本文利用西双版纳植物专著资料, 结合高分辨率的地形和气候等数据, 探讨了面积、边界限制和现代气候对西双版纳野生种子植物物种丰富度及物种密度海拔分布格局的影响。结果表明: (1)物种丰富度呈单峰分布格局, 面积(81.9%)、边界限制(17.5%)和气候(60.0-69.3%)都不同程度地解释了物种丰富度的单峰格局; (2)利用幂函数种-面积关系计算的物种密度沿海拔大致呈减小的分布趋势, 气候的解释率降低为32.6-40.6%, 与边界限制无显著相关关系; (3)利用等面积高度带划分得到的物种密度沿海拔呈单峰变化趋势, 物种密度与边界限制无显著相关性, 但气候对物种密度的解释率为81.6-89.9%。研究结果有助于准确全面地理解物种多样性的海拔分布格局及其成因机制, 为西双版纳生物多样性保护提供理论支撑和实践指导。  相似文献   

2.
Although elevational patterns of species richness have been well documented, how the drivers of richness gradients vary across ecological guilds has rarely been reported. Here, we examined the effects of spatial factors (area and mid‐domain effect; MDE) and environmental factors, including metrics of climate, productivity, and plant species richness on the richness of breeding birds across different ecological guilds defined by diet and foraging strategy. We surveyed 12 elevation bands at intervals of 300 m between 1,800 and 5,400 m a.s.l using line‐transect methods throughout the wet season in the central Himalaya, China. Multiple regression models and hierarchical partitioning were used to assess the relative importance of spatial and environmental factors on overall bird richness and guild richness (i.e., the richness of species within each guild). Our results showed that richness for all birds and most guilds displayed hump‐shaped elevational trends, which peaked at an elevation of 3,300–3,600 m, although richness of ground‐feeding birds peaked at a higher elevation band (4,200–4,500 m). The Normalized Difference Vegetation Index (NDVI)—an index of primary productivity—and habitat heterogeneity were important factors in explaining overall bird richness as well as that of insectivores and omnivores, with geometric constraints (i.e., the MDE) of secondary importance. Granivore richness was not related to primary production but rather to open habitats (granivores were negatively influenced by habitat heterogeneity), where seeds might be abundant. Our findings provide direct evidence that the richness–environment relationship is often guild‐specific. Taken together, our study highlights the importance of considering how the effects of environmental and spatial factors on patterns of species richness may differ across ecological guilds, potentially leading to a deeper understanding of elevational diversity gradients and their implications for biodiversity conservation.  相似文献   

3.
Elevational patterns of species richness and their underlying mechanisms have long been a controversial issue in biodiversity and biogeographical research, and several hypotheses have been proposed in the past decades. Local and regional studies have suggested that area and geometric constraint are two of major factors affecting the elevational pattern of species richness. In this study, using data of seed plants and their distribution ranges and a Digital Elevation Model data set, we explored altitudinal patterns of seed plant richness and quantified the effects of area and the mid-domain effect (MDE) on the richness patterns in a high mountain area, Gaoligong Mountains (ranging from 215 m to 5791 m a.s.l.) located in south-eastern Tibet, China. The results showed that richness and density (richness/log-transformed area) of seed plants at species, genus, and family levels all showed hump-shaped patterns along the altitudinal gradient. The altitudinal changes in richness of species with three different range sizes (< 500 m, 500–1500 m, and > 1500 m), species of different plant life-forms (trees, shrubs, and herbs), and endemic species further confirmed this finding. Analysis of Generalized Linear Model depicted that although the area of each elevational band was always in high correlation with the species richness, the MDE could explain 84.9%, 33.8%, 83.8%, and 84.5% of the total variation in richness for all species and the three species groups with different range sizes, respectively. This suggests that the MDE significantly influences the patterns of species richness and is likely be stronger for broad-ranged species than for narrow-ranged ones in the Gaoligong Mountains.  相似文献   

4.
Aim The decrease in species richness with increasing elevation is a widely recognized pattern. However, recent work has shown that there is variation in the shape of the curve, such that both negative monotonic or unimodal patterns occur, influenced by a variety of factors at local and regional scales. Discerning the shape of the curve may provide clues to the underlying causes of the observed pattern. At regional scales, the area of the altitudinal belts and mass effects are important determinants of species richness. This paper explores the relationship between bird species richness, elevation, mass effects and area of altitudinal zones for birds in tropical mountains. Location The three Andean ranges of Colombia and the peripheral mountain ranges of La Macarena and Santa Marta. Methods Lists of bird species were compiled for altitudinal belts in eastern and western slopes of the three Andean Cordilleras and for La Macarena and Santa Marta. The area of the altitudinal belts was computed from digital elevation models. The effect of area was analysed by testing for differences among altitudinal belts in the slopes and intercepts of the species‐area relationships. Mass effects were explored by separately analysing two sets of species: broadly distributed species, i.e. lowland species whose distributions extend into the Andes, and tropical Andean species, i.e., species that evolved in the Andes. Results Plotting total number of species in each altitudinal belt revealed a decline in species richness with elevation. In slopes with a complete elevational gradient from lowlands to mountain peaks, the decrease was monotonic. In internal Andean slopes where the lower elevational belts are truncated, there was a peak at mid elevations. There was a linear relationship between number of species and area of the altitudinal belts. When controlling for area, there were no differences in the number of species among altitudinal belts (500–2600 m), except for the two upper‐elevation zones (2600–3200 and > 3200 m), which had lower species richness. Diversity of widely distributed species declined monotonically with elevation, whereas tropical Andean species exhibited a mid‐elevation peak. Main conclusions A large proportion of the variation in species richness with elevation was explained by area of the altitudinal belts. When controlling for area, species richness remained constant up to 2600 m and then decreased. This pattern contrasts with a previously reported hump‐shaped pattern for Andean birds. Diversity patterns of widely distributed species suggested that immigration of lowland species inflates diversity of lower elevational belts through mass effects. This influence was particularly evident in slopes with complete altitudinal gradients (i.e. connected to the lowlands). Tropical Andean species, in contrast, were more diverse in mid‐elevational belts, where speciation rates are expected to be higher. The influence of these species was more prevalent in internal Andean slopes with no connection to the lowlands. The decline of species richness at high elevations may be related to higher extinction rates and lower resource levels.  相似文献   

5.
We examined general and family-specific patterns of vascular plant richness along a large elevational gradient (0?C3,670?m a.s.l.), assessed the continuity of these patterns and analysed their potential underlying causes in a high diversity region of the Sierra Madre del Sur, Oaxaca, Mexico. We used a vascular plant database constructed previously. The gradient was divided into 18 200-m elevation belts. To examine elevational patterns of richness, we used both observed and estimated (interpolated) species richness, as well as genus and family observed richness, for each belt. A generalised linear model (GLM) was used to assess the effect of altitude on area-corrected species richness (standard area?=?100?km2), and a numerical classification of the elevational belts based on species richness was performed. Overall, richness at the three taxonomic levels decreased with elevation, but some individual families departed from this pattern. A sharp drop in species richness was observed at 1,800?m, and the dendrogram separated two elevational floristic groups at this elevation. The GLM revealed a significant negative effect of elevation on species richness. Despite this overall decreasing pattern for vascular plants along this extensive gradient, an examination of some family-specific patterns revealed the existence of other elevation?Cdiversity relationships, indicating taxon-specific responses to elevation. The most noticeable discontinuity in species richness, at ca. 1,800?m, is likely related to a critical temperature isocline.  相似文献   

6.
Aim We investigated the patterns of species richness in land snails and slugs along a tropical elevational gradient and whether these patterns correlate with area, elevation, geographic constraints, and productivity. We did so both at the scale at which land snail population processes take place and at the coarser scale of elevational zones. Location Mount Kinabalu (4096 m) and the adjacent Mount Tambuyukon (2588 m) in Kinabalu Park, Sabah, Malaysian Borneo. Methods We used an effort‐controlled sampling protocol to determine land snail and slug species richness in 142 plots of 0.04 ha at elevations ranging from 570 to 4096 m. Extents of elevational ranges were determined by interpolation, extended where appropriate at the lower end with data from lowlands outside the study area. We used regression analysis to study the relationships between species density and richness on the one hand and elevation and area on the other. This was done for point data as well as for data combined into 300‐m elevational intervals. Results Species density (based on the individual samples) showed a decline with elevation. Elevational range length profiles revealed that range lengths are reduced at greater elevations and that a Rapoport effect is absent. Diversity showed a mild mid‐domain effect on Kinabalu, but not on Tambuyukon. When the data were combined into 300‐m elevational intervals, richness correlated more strongly with elevation than with area. Ecomorphospace was seen to shrink with increasing elevation. Main conclusions The elevational species richness patterns show the combined effects of (1) reduced niche diversity at elevations with lower productivity and (2) historical events in which the upward migration of lowland species as well as the speciation of highland endemics took place.  相似文献   

7.
Rapoport's rule applied to an elevation gradient predicts a positive correlation between elevation ranges and elevation. This is supposed to be caused by the increasing magnitude of the climatic extremes at higher elevations, and thus, it is deduced that species richness should decrease with increasing elevation. The distribution of 614 tree species was used to test Rapoport's elevational rule along a gradient from 100 to 4300 m a.s.l., in the Nepalese Himalaya. The relationship between species richness and elevation was analysed by using generalized linear models (GLM). Generalized additive models (GAM) were used to examine the relationship between elevational range and the elevational mid-point of a species along the gradient. The widest elevation ranges are observed at mid-elevations, and narrow elevation ranges are observed at both ends of the gradient. This does not support Rapoport's elevation rule, as proposed by Stevens. There is a peak in species richness between 900 and 1000 m, and not in the tropical lowland as projected by Rapoport's elevation rule.  相似文献   

8.
Understanding the species diversity patterns along elevational gradients is critical for biodiversity conservation in mountainous regions. We examined the elevational patterns of species richness and turnover, and evaluated the effects of spatial and environmental factors on nonvolant small mammals (hereafter “small mammal”) predicted a priori by alternative hypotheses (mid‐domain effect [MDE], species–area relationship [SAR], energy, environmental stability, and habitat complexity]) proposed to explain the variation of diversity. We designed a standardized sampling scheme to trap small mammals at ten elevational bands across the entire elevational gradient on Yulong Mountain, southwest China. A total of 1,808 small mammals representing 23 species were trapped. We observed the hump‐shaped distribution pattern of the overall species richness along elevational gradient. Insectivores, rodents, large‐ranged species, and endemic species richness showed the general hump‐shaped pattern but peaked at different elevations, whereas the small‐ranged species and endemic species favored the decreasing richness pattern. The MDE and the energy hypothesis were supported, whereas little support was found for the SAR, the environmental stability hypothesis, and the habitat complexity. However, the primary driver(s) for richness patterns differed among the partitioning groups, with NDVI (the normalized difference vegetation index) and MDE being the most important variables for the total richness pattern. Species turnover for all small mammal groups increased with elevation, and it supported a decrease in community similarity with elevational distance. Our results emphasized for increased conservation efforts in the higher elevation regions of the Yulong Mountain.  相似文献   

9.
 物种丰富度的分布格局及其形成机制是生态学研究的热点。以往的研究主要描述丰富度的格局, 而对其形成机制研究较少, 且主要集中于探讨单个因子或过程的影响。物种丰富度同时受到多个因子和过程的综合作用, 面积、温度及物种分布区限制被认为是控制山地物种丰富度海拔格局的主要因素, 三者同时沿海拔梯度而变化, 同时作用于丰富度的海拔格局。幂函数种-面积关系(SAR)、生态学代谢理论(MTE)及中域效应假说(MDE)分别基于以上3个因素, 从机制上解释了物种丰富度 的海拔格局。探讨这些假说的相对影响对研究物种丰富度的大尺度格局及其形成机制具有重要意义。方差分离方法有利于分解不同因素的影响, 为此, 该文以秦岭太白山的植物物种丰富度为例, 采用方差分离和逐步回归方法, 分析了SAR、MTE及MDE对物种丰富度海拔格局的影响。结果表明, 太白山的植物物种丰富度沿海拔梯度呈单峰分布格局, 但丰富度峰值存在类群差异; 对太白山所有植物物种丰富度的垂直格局而言, SAR、MTE及MDE分别解释了其物种丰富度随海拔变化的66.4%、19.8%和37.9%, 共同解释了84.6%, 在消除其他因素的影响后, SAR和MTE的独立影响较高(分别为25.5%和17.7%), 而MDE的独立影响不显著; 分类群研究则发现, 苔藓植物丰富度的海拔格局主要受MDE的影响, 蕨类植物丰富度的海拔格局同时受到SAR、MTE以及MDE的影响, 而种子植物物种丰富度的海拔格局主要受SAR和MTE影响。  相似文献   

10.
Two distinct diversity patterns are observed along tropical elevations: (a) decreasing number of species toward high elevations and (b) a hump-shaped pattern with the peak at mid-elevations. As diversity is likely supported by ecological capacity of the environment, decomposition of the overall richness into ecological facets and considering number of individuals within them is crucial for the proper understanding of richness patterns. We examined abundances of different avian guilds along the forested part of the elevational gradient on Mt. Cameroon. We (a) compared richness and abundance elevational patterns, (b) assessed the effective contribution of multiple guilds to richness and abundance patterns, and (c) assessed to what extent observed abundances of guilds differed from those expected by chance. We sampled birds in 2011–2015 during the dry season at seven elevations (30 m, 350 m, 650 m, 1100 m, 1500 m, 1850 m, 2200 m a.s.l.). For each assemblage, we estimated proportions of species and individuals that use particular diets, foraging modes, and feeding strata. We found that a rather decreasing pattern of species richness turns into a hump-shaped one if we look at the total abundances, implying different mechanisms behind these patterns. The number of species and individuals thus do not seem to be directly related, contrary to “the more-individuals hypothesis.” Abundances of foliage gleaners at mid-elevations, nectarivores at high elevations, and frugivores at low elevations deviated from random expectations. Our results imply that parts of ecological space are filled separately by bird species and individuals along elevation of Mt. Cameroon.  相似文献   

11.
The elevational gradient of species richness is often claimed to mirror the latitudinal gradient and has traditionally been explained by assuming a decrease in productivity with elevation and more recently by Rapoport's rule. The influence of area on the pattern has rarely been considered. Analyses of all South American tropical land birds (more than one-fourth of the extant bird species on Earth) are used to examine four species richness/elevation models: null model, Rapoport's rule, and monotonic or hump-shaped productivity/species richness relationships. To quantify the area effect, species-area curves were created for seven elevational zones. Not accounting for area, species richness declined monotonically with elevation, but area accounted for 67%-91% of the variation in species richness per zone. When area was factored out, a hump-shaped pattern emerged, with more species in the 500-1,000-m (P<.005) and 1,000-1,500-m zones (P<.10) than in the 0-500-m zone. Rapoport's rule and the monotonic productivity/species richness relationship were thus not supported. Instead, elevational turnover rates and numbers of shared species between zones suggested that the hump-shaped pattern reflects geometric constraints (as predicted by the null model) imposed by the narrow span of the gradient, and it is suggested that midelevational zones may represent sink habitats.  相似文献   

12.
Abstract. To determine the generality of avian diversity patterns, we investigated patterns of elevational zonation shown by birds and mammals along the eastern slope of the Andes Mountains in southeastern Peru. The strong environmental gradient sampled, entirely within Peru's Manu National Park and Biosphere Reserve, supports highly diverse faunas. Elevational distributions of 901 bird species, 129 bat species, and twenty-eight species of native mice exhibit contrasting patterns in species richness, species composition, and species turnover. Birds and bats showed smooth declines of species richness with elevation, whereas the richness of mouse assemblages was unrelated to elevation. For all three groups, the greatest differences were between lowland and highland faunas, although cutoff points for this contrast varied among groups (≈ 500 m for birds, 750 m for bats, and 1000 m for mice). Differences in composition also separated bird and bat faunas on either side of c. 1400 m (the boundary between montance forest and cloud forest); for mice, this faunal transition may take place nearer to 2000 m. Bird and bat faunas lacked the more discrete zonations suggested for mouse assemblages, as indicated by elevational range profiles and nested subset analyses. Distinct highland assemblages are apparent in two-dimensional histograms of range limits of birds and mice, but not for bats. Highland bat species occupy broader elevational ranges than lowland bat species, but for both birds and mice, species at intermediate elevations had the broadest amplitudes. Finally, clumping of range maxima and minima along the gradient identified zones of pronounced species turnover in each group, but these were generally not strongly associated with the locations of ecotones. Differences in zonation of these groups appear to reflect their different biological attributes and phylogenetic histories. Such differences obviously complicate discussions of ‘general’ diversity patterns, and limit the usefulness of birds to forecast or predict diversity patterns in other more poorly known groups—other groups may show elevated diversity and endemism in areas where avian diversity patterns appear unremarkable. The pronounced contrasts between bats and mice, and the generally intermediate character of avian patterns, suggest that future analyses might profitably partition birds into finer, more homogeneous groups of historically and/or ecologically similar species. Group differences in zonation may ultimately prove explicable with information on both species-abundance patterns and resource distributions.  相似文献   

13.
We used a standard sampling protocol to measure elevational patterns of species richness and abundance of eusocial paper wasps (Hymenoptera: Vespidae) in Costa Rica. The sample transect of six sites spanned approximately 2000 m in elevation from lowland to montane forest. Species accumulation curves and species richness estimates both document a low elevation peak in paper wasp species richness at 50 and 300 m asl, with a decline in species richness at higher elevations. Comparison of species composition among elevations revealed strong species turnover from a rich lowland fauna to a depauperate, but distinct, montane fauna. We also observed a general trend toward a greater abundance of paper wasps at higher elevations, a pattern not usually observed in eusocial insects. Army ant species that prey on paper wasps declined in abundance with elevation across the sample transect, a pattern that has been observed at other sites. We discuss the possibility that elevational changes in predation pressure affect variation in paper wasp abundance and species richness. Eusocial paper wasp species employ one of two modes of colony founding, independent and swarm founding. We found that the total abundance of individual swarm-founding wasps was higher at all elevations than the abundance of independent-founding wasps, supporting previous suggestions that Neotropical swarm founders are more successful ecologically.  相似文献   

14.
Most studies have attempted to identify the major environmental factors responsible for elevational variations in species richness. Such studies have been mainly performed in temperate and tropical areas, whereas the mediterranean biome has been substantially neglected. The aim of this paper was to disentangle the effects of available area, mid-domain constraints, and the environmental tolerance of species, on the altitudinal distribution of tenebrionid beetles in a Mediterranean region. A comprehensive faunistic database was used to assess the elevational distribution of tenebrionids in Latium (Central Italy). Variations in species richness, beta diversity and nestedness were analysed in association with variation in species ranges and midpoints. Variation in species richness was contrasted with patterns expected on the basis of the mid domain effect (MDE) and available surface area. After correcting for differences in area availability due to the conical shape of mountains, an unexpected triphasic pattern emerged: (1) at low altitudes, species richness was higher than expected on the basis of the effect of area and the MDE; (2) at around 800 m elevation, there is an abrupt change in species assemblages, and richness values fit those predicted by the MDE; (3) a new dramatic change occurred at 1,700 m, with tenebrionid assemblages composed of a small number of mainly eurytopic species. The integrated approach used in this study demonstrates that neither MDE nor monotonic patterns fully explain the observed diversity patterns. Variations in species ranges indicate that the elevational gradient filters species according to their ecological tolerance.  相似文献   

15.
Aim We studied pteridophyte species richness between 100 m and 3400 m along a Neotropical elevational gradient and tested competing hypotheses for patterns of species richness. Location Elevational transects were situated at Volcán Barva in the Braulio Carrillo National Park and La Selva Biological Station (100–2800 m) and Cerro de la Muerte (2700–3400 m), both on the Atlantic slope of Costa Rica, Central America. Method We analysed species richness on 156 plots of 20 × 20 m and measured temperature and humidity at four elevations (40, 650, 1800 and 2800 m). Species richness patterns were regressed against climatic variables (temperature, humidity, precipitation and actual evapotranspiration), regional species pool, area and predicted species number of a geometric null model (the mid‐domain effect, MDE). Results The species richness of the 484 recorded species showed a hump‐shaped pattern with elevation with a richness peak at mid‐elevations (c. 1700 m). The MDE was the single most powerful explanatory variable in linear regression models, but species richness was also associated strongly with climatic variables, especially humidity and temperature. Area and species pool were associated less strongly with observed richness patterns. Main conclusions Geometric models and climatic models exclusive of geometric constraints explained comparable amounts of the elevational variation in species richness. Discrimination between these two factor complexes is not possible based on model fits. While overall fits of geometric models were high, large‐ and small‐ranged species were explained by geometric models to different extents. Species with narrow elevational ranges clustered at both ends of the gradient to a greater extent than predicted by the MDE null models used here. While geometric models explained much of the pattern in species richness, we cannot rule out the role of climatic factors (or vice versa) because the predicted peak in richness from geometric models, the empirical peak in richness and the overlap in favourable environmental conditions all coincide at middle elevations. Mid‐elevations offer highest humidity and moderate temperatures, whereas at high elevations richness is reduced due to low temperatures, and at low elevations by reduced water availability due to high temperatures.  相似文献   

16.
The "mid-domain effect" (MDE) has received much attention as a candidate explanation for patterns in species richness over large geographic areas. Mid-domain models generate a central peak in richness when species ranges are placed randomly within a bounded geographic area (i.e. the domain). Until now, domain limits have been described mostly in one-dimension, usually latitude or elevation, and only occasionally in two-dimensions. Here we test 1-D, 2-D and, for the first time, 3-D mid-domain models and assess the effects of geometric constraints on species richness in North American amphibian, bird, mammal and tree species. Using spatially lagged simultaneous autoregressive models, empirical richness was predicted quite well by the mid-domain predictions and the spatial autoregressive term (45–92% R2). However, our results show that empirical species richness peaks do deviate from those of the MDE predictions in 3 dimensions. Variation explained (R2) by MDE predictions generally increased with increasing mean range size of the different biotic groups (from amphibian, to tree, mammal and finally bird data), and decreased with increasing dimensions being accounted for in the models. The results suggest geometric constraints alone can explain much of the variation in species richness with elevation, specifically with respect to the larger-range taxa, birds and mammals. Our analysis addresses many of the recent methodological criticisms directed at studies testing the MDE, and our results support the hypothesis that species diversity patterns are influenced by geometric constraints.  相似文献   

17.
Abstract.  We studied the patterns of species richness and range–size rarity (as a measure of endemism) of two plant groups (Pteridophyta, Bromeliaceae) and birds along two gradients of elevation, humidity and human land use in a forested Andean valley. Both transects covered the transition from an arid valley bottom through a cloud forest zone to relictual high-elevation Polylepis forest, but transects differed in overall precipitation. Plants were surveyed in 88 plots of 400 m2 each, while birds were detected primarily through visual observations and tape recordings over areas of 0.3–1.5 km2. Global range sizes of all species were mapped on 1°-grids and range-size rarity was calculated as the mean inverse range size of all species recorded in elevational steps of 200 m. Patterns of species richness and range–size rarity were mainly unrelated between and within study groups. Monotonic increases and decreases and hump-shaped patterns were observed for species richness as well as range–size rarity. Several of these patterns can be interpreted in the light of the ecological requirements of each taxonomic group, e.g. dependence of fern species richness on humidity or of bird richness on habitat complexity. Species richness of ferns and birds peaked at higher elevations along the less rainy transect, possibly as a result of higher levels of solar radiation and ecosystem productivity. Patterns of species richness and endemism of the study groups are causally unrelated and cannot be used to predict those of other groups at the spatial scale of this study. Human impact was highest in areas of mostly low to intermediate species richness, but was often high in zones of high endemism.  相似文献   

18.
We sampled terrestrial molluscs at fifteen elevations between 400 and 2000 m in Mwanihana Forest Reserve, Tanzania and recorded 84 taxa. Four diversity measures – species density (DP), species richness (D20) and observed (SO) and interpolated (SI) alpha diversity – were measured; beta diversity and abundance were also investigated. Mean elevational range was 470 m. DP, D20, alpha diversity and mollusc abundance increased with elevation, but alpha diversity peaked at 1695 m (SO) or 1500 m (SI) and declined at higher elevations. Maximum beta diversity was at 1000 m. Soil pH was negatively correlated with elevation and DP. Cluster analysis divided the sites into lowland (400–900 m) and highland (>1000 m) groups. Axis 1 of a canonical correspondence analysis was associated with altitude and suggested a faunal discontinuity at 1000 m. Variation within the highland (>1000 m) and lowland faunal sets was related to elevation and forest structure respectively. The findings indicate that mollusc diversity peaks at intermediate elevations. This may be related to the combined effects of low rainfall conditions at low elevations and increasing effects of soil leaching at high elevations, both of which may limit mollusc diversity and abundance. Diversity at intermediate altitudes may be further elevated because of faunal mixing of lowland and highland groups.  相似文献   

19.
Kessler  Michael 《Plant Ecology》2000,149(2):181-193
I analyzed the distribution of Acanthaceae, Araceae, Bromeliaceae, Cactaceae, Melastomataceae, and Pteridophyta in 62 vegetation plots of 400 m2 along an elevational transect between 500 m and 2450 m, and at a nearby lowland site in western Santa Cruz department, Bolivia. These groups were selected because they are physiognomically distinctive, have high species numbers, are comparatively easy to identify, adequately reflect overall floristic relationships, include a wide range of life forms, and are small. The transect was located in the Tucumano-Boliviano biogeographic zone and included drought-deciduous (<850–1000 m), mixed evergreen (850–1000 m to 1800 m), and evergreen Podocarpus-dominated (>1800 m) forests. Elevational patterns of species richness were group-specific and probably related to the ecophysiological properties of each group. Species richness in Pteridophyta and Melastomataceae was correlated with moss cover (i.e., humidity), with elevation (i.e., temperatures) in Acanthaceae and epiphytic Bromeliaceae, with potential evapotranspiration (i.e., ecosystem productivity) in Araceae, and with light availability at ground level in terrestrial Bromeliaceae and Cactaceae. Community endemism generally increased with elevation, but showed a maximum at 1700 m for terrestrial Pteridophyta, and a nonsignificant decline for epiphytic Bromeliaceae and Cactaceae. Endemism was higher for terrestrial than for epiphytic taxa, and was lower among Pteridophyta compared to all other groups, reflecting different dispersal ability among taxonomic and ecological groups. Elevational zonation, tested against a null-model of random distribution of elevational limits, revealed a significant accumulation of upper and lower elevational range boundaries at 900–1050 m and at 1500–1850 m, corresponding to the elevational limits of the main physiognomic vegetation types.  相似文献   

20.
猫儿山是华南地区的最高峰,为了了解其鸟类随着海拔高度变化的规律,利用网捕法和样线法对猫儿山地区的鸟类组成及分布格局进行了研究。结果表明,猫儿山地区共有鸟类268种,隶属于16目51科,其中留鸟130种,夏候鸟51种,冬候鸟15种,旅鸟72种。依据不同海拔的典型植被类型把猫儿山地区分成7类生境,其中低海拔的农田生境鸟类多样性最丰富,有156种。随着海拔的升高,猫儿山鸟类种数逐渐减少,G-F指数也表现相似的规律。猫儿山鸟类在区系组成上主要以东洋界鸟类为主,在181种繁殖鸟中,东洋界鸟类有149种,古北界鸟类有15种,其余为广布种。随着海拔的升高,东洋界的鸟类所占的比例逐渐降低,而古北界的鸟类所占的比例逐渐升高。猫儿山鸟类组成的垂直分布格局的形成是多种因素共同作用的结果。  相似文献   

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