喀斯特山区植物物种丰富度的空间变异分析

应用地统计学对地处滇黔桂连片喀斯特腹地的贵州省毕节地区植物物种丰富度的海拔空间变异进行分析。结果表明,乔木物种丰富度的半变异函数最佳理论模型为球状模型,灌木、草本为线性有基台模型。乔木物种丰富度的空间异质比为0．0052,具有强烈的海拔空间相关性,主要受随海拔梯度变化的自然性控制因素的影响;灌木、草本物种丰富度的空间异质比分别为3．15、34．55,海拔梯度的空间相关性很弱,受随机因素作用较大。乔木物种丰富度的变程为177．37m受因素影响的海拔范围较宽;灌木和草本物种丰富度的变程分别为73．02m和49．97m,受因素影响的海拔范围较窄。灌木、草本物种丰富度的Moran’s I系数随海拔梯度变化的趋势相类似,但乔木的差别较大。     

福建梅花山常绿阔叶林植物物种多样性及其海拔梯度格局

常绿阔叶林是福建梅花山国家级自然保护区地带性植被。采用样带与典型群落调查法对区内的常绿阔叶林14400m2样地展开调查,并对植物多样性海拔梯度格局进行分析,结果表明：（1） 群落植物物种丰富度、Gleason丰富度指数、Simpson指数、Shannon Wiener指数和Pielou均匀度指数的均值分别为64.42、10.75、5.75、3.50、0.58,且这5种指数在各样带间差异极为显著,并随海拔的升高均呈单峰曲线变化,峰值出现在海拔700m~900m。（2） 群落各层次的植物物种丰富度、Shannon Wiener指数均呈现灌木层（包括幼树和层间植物）〉乔木层〉草本层的特征。乔木、灌木层物种丰富度与乔木层Shannon Wiener指数在海拔梯度上的样带间差异极显著,变化趋势与群落相似;灌木层与草本层Shannon Wiener指数以及草本层物种丰富度随海拔梯度变化不明显。因此,梅花山自然保护区常绿阔叶林植物物种多样性的海拔梯度格局呈现单峰分布,并支持中间高度膨胀模式（mid domain model）。     

高黎贡山种子植物物种丰富度沿海拔梯度的变化

物种丰富度沿海拔梯度的分布格局成为生物多样性研究的热点。为探讨中尺度区域物种丰富度沿海拔梯度的分布,本文以高黎贡山为研究对象,利用该地区的地方植物志资料,结合通过GIS生成的区域数字高程模型(DEM)数据,分析了该区域全部种子植物和乔木、灌木、草本三种生活型种子植物物种丰富度的垂直分布格局以及物种密度沿海拔梯度的变化特征。结果表明：(1)全部种子植物和不同生活型植物物种丰富度随着海拔的升高呈现先增加后减小的趋势,最大值出现在海拔1500—2000m的范围;(2)物种密度与海拔也呈现单峰曲线关系;(3)物种丰富度和物种密度分布格局的形成主要受海拔所反映的水、热状况组合以及物种分布的边界影响。     

北京东灵山地区植物群落多样性研究 Ⅹ.不同尺度下群落样带的β多样性及分形分析

选取不同尺度,采用β多样性指数和分形分析方法对东灵山暖温带森林样带上群落多样性随海拔梯度的空间变异规律进行了研究。结果表明,１）Ｃｏｄｙ指数揭示出乔木层在取样尺度２０ｍ和灌木层在取样尺度８０ｍ时,随海拔梯度变化呈明确的物种替代规律性;乔木层和灌木层在同一地点的物种替代速率具有互补性;群落多样性的空间变异在样带的起始（山底）和终止（山顶）地段较高。２）笔者提出的群落结构变异（ＣｏｍｍｕｎｉｔｙＳｔｒｕｃｔｕｒｅＶａｒｉａｔｉｏｎ,ＣＳＶ）指数介于０～１之间,作为Ｃｏｄｙ指数的改进,它对群落多样性沿环境梯度变化的揭示更接近于实际情况;ＣＳＶ指数分析显示乔木层在＞４０ｍ取样尺度,灌木层＞２０ｍ取样尺度群落结构出现明确变异规律;物种丰富度（Ｃｏｄｙ指数）和群落结构（ＣＳＶ指数）变化规律性的表现尺度（取样尺度）不同。３）分形分析的结果,乔木主林层在２００ｍ内不同尺度间不存在相关规律,乔木更新层只在＜４０ｍ尺度显示出尺度依赖性,灌木层的尺度依赖特征则表现为小尺度变异显著而较大尺度上变异程度降低;乔木更新层与灌木层的异质性规律发生显著变化（拐点）的尺度不同,分别为４０ｍ和９０～１００ｍ。同时,还对群落学研究中的取样尺度问题进行了探讨。     

北京松山自然保护区森林群落物种多样性及其神经网络预测

物种多样性是群落结构和功能复杂性的一种度量,物种多样性的空间分布格局受许多环境因子的影响.运用多样性指数,多层感知器网络,分析了松山保护区森林群落物种多样性与群落类型、结构和生境之间的关系.结果表明:(1)大果榆+山杨混交林、油松+青杨混交林物种丰富度、多样性和均匀度均较高,而大果榆林、华北落叶松林的各项指数值均较低.Patrick指数和Shannon-Weiner指数在森林群落中均表现为草本层＞灌木层＞乔木层;Pielou指数在榆林中表现为草本层＞乔木层＞灌木层,而在其他森林群落中表现为灌木层＞草本层＞乔木层.(2)功能层物种多样性在海拔梯度上的变化趋势不同,在乔木层,丰富度、多样性和均匀度随海拔的升高逐渐降低;在灌木层,丰富度、多样性和均匀度均呈比较明显的单峰曲线变化趋势;在草本层,丰富度和多样性随海拔的升高都呈下降趋势,而在草本层,均匀度变化不大.(3)用多层感知器网络预测功能层多样性效果很好,结果发现坡向对乔木层和灌木层物种多样性的影响最大,而海拔高度对草本层物种多样性的影响最大.     

百花山植物群落物种多样性研究

基于百花山50个样方的调查资料，从不同类型群落的物种多样性及其与海拔的关系等方面对百花山植被进行了分析，并且用DCA排序和海拔高程排序对物种多样性在环境梯度上的分布格局进行了初步研究。结果表明：群落内不同生长型的物种丰富度指数在森林群落中大小顺序为草本层＞灌木层＞乔木层，灌丛群落主要表现为草本层﹥灌木层，只有荆条灌丛表现为灌木层＞草本层；Shannon-Wiener指数在山杨—华北落叶松群落中表现为灌木层＞草本层＞乔木层,其他森林群落为草本层＞灌木层＞乔木层，在灌丛群落中主要表现为草本层＞灌木层，只有荆条灌丛表现为灌木层＞草本层；均匀度指数在灌丛群落中表现为灌木层＞草本层，在辽东栎林和山杨—华北落叶松林中表现为灌木层＞乔木层＞草本层,而其他森林群落表现为乔木层＞灌木层＞草本层。物种多样性在DCA第一轴排序和海拔高程梯度上都表现出单峰曲线变化趋势，但拟和效果的显著程度不同：丰富度和均匀度指数在海拔高程上曲线的拟和效果优于DCA环境梯度排序效果；而多样性指数则相反。     

香溪河流域河岸带植物群落物种丰富度格局

通过不同海拔高度的样带调查来研究香溪河流域河岸植物群落物种丰富度格局,并探讨河岸带中生物多样性维持的生态学机制。结果表明：河岸植物群落总的物种丰富度、乔木层物种丰富度和草本层物种丰富度沿海拔梯度均表现出相似的格局特征,利用抛物线方程进行拟合,物种丰富度与海拔之间有显著的相关性。灌木层物种丰富度和藤本植物物种丰富度格局特征不明显,且物种丰富度与坡度相关,在流域尺度上,海拔对物种丰富度有着重要的控制作用;在局部尺度上,季节性洪水干扰导致的空间异质性和小地形对群落的生物多样性有着重要的影响,研究结果支在于总的物种多样性在原始河流的中间河段将达到最大值的预测。     

地形对七姊妹山自然保护区植物丰富度及分布格局的影响

该研究以七姊妹山自然保护区40个(20×20m2)植物群落调查样方为基础,并采用回归分析和典型对应分析(CCA)的方法研究该区地形对植物物种丰富度及植物分布格局的影响,以明确海拔、坡度、坡向、坡位等地形因子的相对重要性,为该区植物多样性的保护和管理提供理论依据。结果表明:(1)七姊妹山自然保护区40个调查样地共有植物633种,隶属133科,316属,其中乔木118种,灌木150种,草本365种。(2)曲线回归方程拟合结果显示,七姊妹山自然保护区植物物种丰富度分别与海拔、坡度具有显著相关性,物种丰富度沿海拔梯度升高而增大,沿坡度梯度先减少后增大之后又减小。(3)从植物的生活型来看,在所有海拔段,乔木物种丰富度始终低于灌木和草本植物;在低、中低海拔地带,灌木物种丰富度均高于乔木和草本植物;而在中、高海拔地带草本植物物种丰富度较大且高于乔木和灌木。(4)CCA排序结果表明,地形因子对植物物种的分布具有显著影响按其影响强度排序为海拔坡度坡位坡向,说明海拔是影响该区植物物种分布最重要的地形因子。     

长白山北坡植物群落组成、结构及物种多样性的垂直分布

通过沿海拔梯度的系统调查,运用TWINSPAN分类方法,划分出长白山北坡的主要植物群落类型,对这些群落的组成和结构进行了分析。利用物种丰富度、α多样性和β多样性等指标,研究了群落多样性随海拔梯度的变化趋势。结果表明,乔木层植物可分为4个群落类型：从低海拔到高海拔依次为红松(Pinus koraiensis)针阔混交林、红松针阔叶树种与云冷杉组成的过渡群落、云冷杉暗针叶林以及岳桦林(Betula ermanii)。乔木层优势种重要值的分析清楚地反映出长白山北坡植被垂直带谱的优势成分。径级频度分布的分析表明该区域主要群落的自我更新状况良好。植物物种多样性随海拔梯度的变化趋势为：随海拔升高,乔木层和灌木层的物种丰富度呈下降趋势,但草本层的变化趋势不明显;乔木层和灌木层的α多样性(Shannon-Wiener指数)呈下降趋势,草本层则变化不明显;无论是木本层还是草本层的Pielou均匀度指数均没有明显的变化;乔木层、灌木层和草本层植物的β多样性(Cody指数)均随着海拔的升高而下降。     

祁连山北坡中段植物群落多样性的垂直分布格局

利用DCCA排序和海拔高程排序相结合的方法 ,对祁连山北坡中段植物群落物种多样性垂直分布格局进行了初步研究。结果表明 :1)植物群落草本层和灌木层物种丰富度和多样性在环境梯度上呈单峰曲线变化趋势 ,乔木层的物种丰富度和多样性在环境梯度上无变化。物种丰富度和多样性对环境梯度变化敏感程度的次序是草本层 >灌木层 >乔木层 ;2 )植物群落各层次均匀度在环境梯度上没有表现出一定的变化规律 ,均匀度可能更多地受制于群落自身动态的影响 ,而独立于生境的资源水平 ;3)草地群落物种多样性在DCCA环境梯度上曲线的拟合效果优于按海拔高程排序效果 ,灌木群落则相反 ;4)低海拔、中低海拔和中海拔地带的草本层物种丰富度和Shannon Wiener多样性指数 (H′)显著高于灌木层 (p <0 .0 1) ;高海拔地带草本层仅丰富度指数显著高于灌木层 (p <0 .0 5 )。在整个海拔范围内 ,草本层和灌木层的均匀度无显著差异。就资源的可利用性而言 ,研究区域植物群落物种多样性在垂直环境梯度上的变化规律表达了物种多样性与资源生产力的单调关系内涵。     

Distribution of Vascular Plant Species Richness Along an Elevational Gradient in the Dongling Mountains, Beijing, China

Quantifying spatial patterns of species richness and determining the processes that give rise to these patterns are core problems In blodlveralty theory. The aim of the present paper was to more accurately detect patterns of vascular species richness at different scales along altitudinal gradients in order to further our understanding of biodlverslty patterns and to facilitate studies on relationships between biodiversity and environmental factors. Species richness patterns of total vascular plants species, including trees, shrubs, and herbs, were measured along an altitudinal gradient on one transect on a shady slope in the Dongling Mountains, near Beijing,China. Direct gradient analysis, regression analysis, and geostatistics were applied to describe the spatial patterns of species richness. We found that total vascular species richness did not exhibit a linear pattern of change with altitude, although species groups with different ecological features showed strong elevational patterns different from total species richness. In addition to total vascular plants, analysis of trees, shrubs, and herbs demonstrated remarkable hierarchical structures of species richness with altitude (i.e. patchy structures at small scales and gradients at large scales). Species richness for trees and shrubs had similar spatial characteristics at different scales, but differed from herbs. These results indicated that species groups with similar ecological features exhibit similar biodlveraity patterns with altitude, and studies of biodiversity based on species groups with similar ecological properties or life forms would advance our understanding of variations in species diversity. Furthermore, the gradients or trends appeared to be due mainly to local variations in species richness means with altitude. We also found that the range of spatial scale dependencies of species richness for total vascular plants, trees, shrubs, and herbs was relatively large. Thus, to detect the relationships betweenspecies richness with environmental factors along altitudinal gradients, it was necessary to quantify the scale dependencies of environmental factors in the sampling design or when establishing non-linear models.     

三江并流地区干旱河谷植物物种多样性海拔梯度格局比较

在滇西北三江并流地区典型干旱河谷段, 在怒江、澜沧江和金沙江的东、西坡共设置了6条海拔梯度样带, 通过标准样地的植物群落调查, 分析各条样带植物的物种丰富度、物种更替率的海拔梯度格局, 并比较了地理和植被变量对分布格局的解释。干旱河谷植被带位于海拔3,000 m以下, 以灌丛和灌草丛为主, 其在各河谷的分布上限自西向东依次升高。植物物种丰富度的分布主要与海拔、流域、经纬度和植被带有关, 沿纬度和海拔梯度升高而显著增加的格局主要表现在草本层和灌木层, 灌木物种丰富度还呈现自西向东显著增加的趋势。怒江的灌木和草本种物种丰富度显著高于金沙江和澜沧江, 三条江的乔木种丰富度差异则不显著。森林带的样方草本物种丰富度显著低于灌草丛带样方, 并且还拥有后者没有的乔木种。不同样带的植物物种更替速率呈现了不一致的海拔梯度格局, 但均在样带海拔下部的灌草丛群落与海拔上部森林群落之间的交错带出现峰值。森林-灌草丛植被交错带在怒江样带处于海拔1,900-2,100 m处, 在澜沧江河谷位于海拔2,300-2,400 m, 在金沙江河谷位于海拔2,700-2,900 m。所有海拔样带的森林段或灌草丛段相对于同一样带不同植被段之间的物种更替程度为最小, 不仅小于同一流域不同样带相同植被段之间物种更替率的均值, 更小于所有样带相同植被段之间的更替率均值。在三条河流6条海拔样带的12个植被带段之间的物种更替变化中, 空间隔离因素可以解释34.2%, 而植被类型差异仅能解释不到0.5%。本研究结果显示了环境差异对不同植被类型物种丰富度的首要影响, 和各河流之间的空间隔离对植物群落构建和物种构成的主要作用。     

Continuum or zonation? Altitudinal gradients in the forest vegetation of Mt. Kilimanjaro

Based on the analysis of 600 vegetation plots using the method of Braun-Blanquet (1964) the composition of the whole vascular forest plant flora with about 1220 species was studied in the forests of Mt. Kilimanjaro. The altitudinal distribution of all strata (trees, shrubs, epiphytes, lianas and herbs) along a transect of 2400 m is discussed with respect to altitudinal zonation and ecological factors. With uni-dimensionally constraint clustering significant discontinuities were revealed that occurred simultaneously in the different strata. Thus even in structurally highly complex, multilayered tropical montane forests distinct community units exist that can be surveyed and classified by the Braun-Blanquet approach. This observed zonation was significantly correlated with altitude, temperature and soil acidity (pH); rainfall was of importance in particular for the zonation of epiphytes. Other key factors were humidity (influenced by stable cloud condensation belts) and minimum temperature (in particular the occurrence of frost at 2700 m altitude upslope). The contrary results of other transect studies in East Africa in respect to continuity of change in floristic composition appear to be caused by different sampling methods and intensities or mixing of data from areas with different climate conditions, whereas species richness did not influence the clarity of floristic discontinuities on Kilimanjaro and other parts of East Africa.     

Elevational plant species richness patterns and their drivers across non-endemics,endemics and growth forms in the Eastern Himalaya

Despite decades of research, ecologists continue to debate how spatial patterns of species richness arise across elevational gradients on the Earth. The equivocal results of these studies could emanate from variations in study design, sampling effort and data analysis. In this study, we demonstrate that the richness patterns of 2,781 (2,197 non-endemic and 584 endemic) angiosperm species along an elevational gradient of 300–5,300 m in the Eastern Himalaya are hump-shaped, spatial scale of extent (the proportion of elevational gradient studied) dependent and growth form specific. Endemics peaked at higher elevations than non-endemics across all growth forms (trees, shrubs, climbers, and herbs). Richness patterns were influenced by the proportional representation of the largest physiognomic group (herbs). We show that with increasing spatial scale of extent, the richness patterns change from a monotonic to a hump-shaped pattern and richness maxima shift toward higher elevations across all growth forms. Our investigations revealed that the combination of ambient energy (air temperature, solar radiation, and potential evapo-transpiration) and water availability (soil water content and precipitation) were the main drivers of elevational plant species richness patterns in the Himalaya. This study highlights the importance of factoring in endemism, growth forms, and spatial scale when investigating elevational gradients of plant species distributions and advances our understanding of how macroecological patterns arise.     

新疆天山南坡中段种子植物区系垂直分布格局分析

对植物多样性垂直分布格局及其维持机制的研究可以有效揭示植物物种多样性分布特征及其环境影响因子。本文通过野外调查、查阅标本并结合相关文献资料,对天山南坡中段种子植物区系沿海拔梯度的分布格局进行了系统研究。结果显示,在大区域尺度上,科属种的物种丰富度随海拔升高均呈先增加后减少的趋势,且最高值出现在中低海拔1900~2000 m处;不同生活型植物沿海拔梯度的变化格局有所不同,其中,乔木、一年生草本、藤本及寄生植物表现出随海拔升高物种丰富度逐渐降低的趋势,灌木、多年生草本及二年生草本植物物种丰富度则呈先增加后减少的变化趋势;从植物区系地理成分来看,世界分布所占的比重沿海拔梯度升高呈先增加后减少的趋势;温带地理成分所占的比重沿海拔梯度升高呈缓慢上升趋势;古地中海地理成分所占的比重沿海拔梯度升高呈先增加后减少然后再增加的变化趋势;热带地理成分所占的比重沿海拔升高呈逐渐下降的趋势;东亚地理成分所占的比重沿海拔梯度升高呈先增加后减少然后再增加的变化趋势。对该分布格局与当地干旱的气候条件及海拔梯度上热量和水分条件的变化相适应。     

Influence of altitude on the distribution pattern of flora in a protected area of Western Himalaya

IntroductionDistribution pattern and diversity of flora was compared along an altitudinal gradient using the stratified random sampling design for identifying major plant communities of Kedarnath Wildlife Sanctuary of Garhwal Himalaya, India. The reconnaissance of flora is presented, along with the analysis of the distribution of species, genera, and families within five (5) altitudinal zones. Kedarnath Wildlife Sanctuary which is situated in the Indian Himalayas harbours a rich variety of flora and fauna. The Himalayas are recognized for diverse vegetation distributed over a wide range of topographical conditions.ResultsThe analysis of diversity within five (5) altitudinal zones was carried out and a total of 324 plant species, representing 219 genera belonging to 92 families, were found. The dominant family was Asteraceae; the co-dominant family was Rosaceae, followed by Lamiaceae and Ranunculaceae. Eight (8) families were observed in all the altitudinal zones, while forty (40) families were observed in a single altitudinal zone, and the remaining forty-four (44) families were found in more than one (1) altitudinal zone. Most of the tree species were contagiously distributed, but a few of them were randomly distributed in all the altitudinal zones. The shrubs and herbs were contagiously distributed in all the altitudinal zones. The correlation analysis (P < 0.05) between altitude and number of species showed that altitude is negatively correlated with tree (r = −0.96), shrub (r = −0.61), and herb species (r = −0.20). As per the cluster analysis of tree layer, altitudinal zone - III (2450–2650 m) and altitudinal zone - IV (2900–3100 m) were found most similar. Altitudinal zone–V (3350–3550 m) was found to be dissimilar from the other zones for herbs.ConclusionsAlthough species composition varies with altitude, but there is a complex relationship between species richness and altitudinal gradient. A decreasing pattern in both species richness and family richness for trees, shrubs and herbs, was recorded with increasing altitude. The predominant factors underlying this variability in plant species and biogeography appear to be climatic and specific to each taxonomic group.     

Vascular plant diversity and climate change in the alpine zone of the Snowy Mountains,Australia

This study examines vascular plant species richness along an altitudinal gradient in alpine Australia. Vascular plant composition and soil temperature records were obtained for five summits (from 1729 m to 2114 m a.s.l.) using sampling protocols from the Global Observation Research Initiative in Alpine Environments program. Species richness was examined against altitude, aspect and climatic variables at different spatial scales (10 × 10 cm quadrats, 1 m² quadrats, clusters of 4 * 1 m² quadrats, for the summit area above a line 5 m altitudinally below the summit (the −5 m isoline), for the extended summit down to the −10 m isoline). About 75 taxa (70 species, 5 graminoid genera) were recorded, 9 of which are endemic to the small alpine area of ∼100 km². There were significant linear relationships between species richness and altitude and climatic variables for the top to −5 isolines on the summits. However, there was no consistent pattern for species richness at other spatial scales, altitude, aspect or climatic variables. The proportion of species for the whole summits with localised distributions (local endemics) increased with altitude. Predicted increasing temperatures and reduced snowcover is likely to result in an increase in species richness as shrubs, herbs and introduced weeds become more common at higher altitude. Because Australian alpine areas occur in narrow altitudinal bands with no nival zone, there are no higher altitudinal refuges available for alpine species. Therefore many of these species are likely to be at risk of extinction from climate change.     

Plant invasion and speciation along elevational gradients on the oceanic island La Palma,Canary Islands

Ecosystems that provide environmental opportunities but are poor in species and functional richness generally support speciation as well as invasion processes. These processes are expected not to be equally effective along elevational gradients due to specific ecological, spatial, and anthropogenic filters, thus controlling the dispersal and establishment of species. Here, we investigate speciation and invasion processes along elevational gradients. We assess the vascular plant species richness as well as the number and percentage of endemic species and non‐native species systematically along three elevational gradients covering large parts of the climatic range of La Palma, Canary Islands. Species richness was negatively correlated with elevation, while the percentage of Canary endemic species showed a positive relationship. However, the percentage of Canary–Madeira endemics did not show a relationship with elevation. Non‐native species richness (indicating invasion) peaked at 500 m elevation and showed a consistent decline until about 1,200 m elevation. Above that limit, no non‐native species were present in the studied elevational gradients. Ecological, anthropogenic, and spatial filters control richness, diversification, and invasion with elevation. With increase in elevation, richness decreases due to species–area relationships. Ecological limitations of native ruderal species related to anthropogenic pressure are in line with the absence of non‐native species from high elevations indicating directional ecological filtering. Increase in ecological isolation with elevation drives diversification and thus increased percentages of Canary endemics. The best preserved eastern transect, including mature laurel forests, is an exception. The high percentage of Canary–Madeira endemics indicates the cloud forest's environmental uniqueness—and thus ecological isolation—beyond the Macaronesian islands.