不同植物类群物种丰富度垂直格局分形特征的比较

格局和过程一直是生态学的核心问题,该文应用“非布朗运动随机分形”模型,在北京东灵山远离人为干扰地区的阴坡设置了两条宽2 m的样带,描述和比较了暖温带落叶阔叶林区乔木、灌木、草本以及总的植物物种丰富度在不同尺度上沿海拔梯度变异特征,以及相关的生态过程。研究结果表明:1)直接梯度法刻画了植物物种丰富度在海拔梯度上的总体变化趋势,并不能从中获得更多的信息。“非布朗运动随机分形”模型揭示了不同尺度上物种丰富度的空间变化并能和生态过程相联系,研究表明该模型适合对乔木、灌木和草本植物物种丰富度的垂直梯度格局特征进行描述,但对总的植物物种丰富度有一定的局限性。2)乔木物种丰富度在海拔梯度上的变化主要受两种生态过程的控制,小尺度上分形维数接近于2,主要受独立的不具有长程相关的生态过程控制,呈近随机分布;大尺度上分形维数接近于1,主要受自相关范围大、具有长程关联特性的生态过程控制,随海拔上升呈近似单调下降的趋势。灌木和草本物种丰富度在海拔梯度上的变化主要受3种生态过程的控制,小尺度和大尺度上的特征与乔木相似;但在中等尺度上,分形维数接近于1.5,它们以近似布朗运动的形式变化。虽然乔木和灌木物种丰富度在海拔梯度上变化的尺度范围相似,但决定它们的主要生态过程完全不同,或相同的生态过程以截然不同的方式作用于两种不同的植物类群。总的植物物种丰富度在整个尺度范围内呈现标度不变性,这可能是由于决定其变化的生态过程作用尺度紧密相关,也可能因为该文研究范围的局限性。     

面积和中间膨胀效应对丽江地区种子植物物种丰富度垂直分布格局的影响

滇西北地区是我国三大特有物种分化中心之一。作者利用地方植物志资料,结合数值高程模型(DEM)数据,研究了云南丽江地区种子植物物种丰富度的垂直分布格局,并分析了面积和中间膨胀效应(mid-domaineffect)对该格局的影响。研究结果表明:随着海拔的升高,各海拔段面积呈先增加后下降的分布格局;物种丰富度、物种密度和中间膨胀效应的物种丰富度预测值在海拔梯度上均呈单峰型变化格局。面积和中间膨胀效应对丽江地区物种丰富度的垂直分布格局有着显著的影响。其中,面积起主要作用,对物种丰富度的变异解释百分率达80.2%,而中间膨胀效应的影响作用相对较小,仅占11.3%。     

茂兰喀斯特森林植物物种丰富度的垂直分布特征及环境解释

茂兰喀斯特峰丛地貌森林是目前罕见的一类原生性强、人为干扰少的非地带性森林生态系统,与常态地貌地带性森林生态系统相比差异大。该研究采用典型样地调查方法对茂兰喀斯特森林海拔在620～910 m之间的垂直样带11个样方进行调查,分析研究区顶级群落物种丰富度的垂直梯度变化特征,并用冗余分析(RDA)法分析环境因子对物种丰富度的影响,以明确垂直梯度上物种丰富度与环境因子的关系,为喀斯特自然森林生态系统的维持与恢复、保护与管理提供理论基础。结果表明：(1)该调查茂兰喀斯特峰丛共记录有维管植物511种,隶属于124科272属。(2)单因素方差分析表明,该群落不同生活型的丰富度之间存在极显著差异(P<0.01);LSD多重比较分析表明,群落丰富度水平表现为总体>灌木层>草本层>乔木层。(3)随海拔梯度的升高,群落总物种丰富度和草本层物种丰富度与海拔呈显著负相关关系(P<0.05),乔木层丰富度和灌木层丰富度与海拔无明显规律。(4)冗余分析表明,土壤C/N/P的解释率达到58%,是影响物种丰富度的主要因素。     

新疆喀纳斯旅游区树种多样性垂直格局与自然火干扰

采用典型样带调查法,通过对新疆喀纳斯旅游区树种多样性垂直格局及其与自然火干扰分布关系的研究,揭示了树种多样性沿海拔梯度的分布格局及其对自然火干扰的响应特征.结果表明:①树种多样性随海拔的升高呈现明显的下降态势(P＜0.01),但树种多样性与海拔高度之间的相关程度不高(R2=0.2165),并且表现出以1900m为界的区域性变化特征.②所调查范围内共发生了8次自然火干扰事件,平均间隔时间为14a,干扰事件多集中在1900m以下的较低海拔区.③林分受自然火干扰作用后,树种多样性普遍表现出增加的特征.总体而言,海拔高度是影响喀纳斯森林群落树种多样性垂直分布格局形成的基本因素,但随机发生的自然火干扰是主导1900m以下较低海拔区树种多样性丰富的关键因素之一.     

秦岭小陇山保护区维管植物丰富度和种域海拔梯度格局及其对Rapoport法则验证

物种丰富度和种域的海拔梯度格局及其形成机制一直是生物地理学和生物多样性研究的重点.海拔Rapoport法则认为,物种丰富度随海拔升高而逐渐降低,种域逐渐变宽.本文分析了秦岭小陇山国家级自然保护区维管植物物种丰富度及其种域宽度的海拔梯度格局;采用4种常用方法,验证不同类群、不同生长型和不同阶元的物种丰富度与其分布中点间的关系,并检验其是否支持海拔Rapoport法则.结果表明: 除窄域种外,秦岭小陇山维管植物物种丰富度随海拔升高呈先升后降的单峰分布格局;狭域种主要分布在低海拔和高海拔段,低海拔段的丰富度高于高海拔段;物种海拔分布宽度与海拔关系因不同类群和验证方法而异,随分类阶元的增大更容易支持Rapoport法则,这可能与不同分类阶元所占据的生态位不同有关;被子植物的平均种域呈单峰分布格局,蕨类植物和裸子植物的种域海拔梯度格局无明显规律;藤本植物平均种域随海拔升高而变宽,灌木能适应不同的环境条件,因此,灌木分布对海拔梯度的变化不敏感.Pagel验证方法最容易支持Rapoport法则,Stevens方法次之,中点法受中域效应的影响物种平均种域分布呈单峰分布格局而不支持Rapoport法则,逐种法受散点图分布格局的影响线性模型拟合结果解释力很低.
     

南岭东西段植物群落物种组成及其树种多样性垂直格局的比较

根据沿海拔梯度设置的样地的调查资料,对南岭东段的莽山和西段的猫儿山植物群落乔木层物种多样性的垂直分布格局进行了比较研究。莽山和猫儿山的植被类型差异不大,但相同植被类型的物种组成有比较明显的差异。随海拔的上升,两山体乔木的最大树高均呈现显著下降趋势。猫儿山乔木的最大胸径、胸高断面积之和以及立木密度在海拔梯度上呈单峰曲线变化趋势。莽山乔木的最大胸径、胸高断面积之和与海拔呈明显的负相关性,而立木密度的变化规律不明显。这种单峰曲线格局或负相关关系与中尺度上的海拔高度以及小尺度上的土壤特性、小地形以及人为干扰强度等因素有关。在海拔1000m以下的常绿阔叶林群落和1700m以上的山顶矮林群落,莽山乔木的物种丰富度均明显高于猫儿山。两山体的乔木种数与海拔之间都显示出负相关性,但莽山由于高海拔群落受人为干扰的影响,这种相关性不显著。乔木层α多样性沿海拔梯度没有表现出明显的变化规律,并且在两山体之间也看不出明显的差别。本文最后还对两山脉低海拔区段的常绿阔叶林群落的物种组成和多样性进行了对比分析,结果表明人为干扰导致猫儿山常绿阔叶林的物种丰富度(S)和α多样性(H’)明显低于莽山的原生性常绿阔叶林群落,而且落叶阔叶树种和毛竹(Phyllostachys pubescens)开始入侵到群落中。     

基于等面积高度带划分的贺兰山维管植物物种丰富度的海拔分布格局

山地植物物种丰富度海拔分布格局是生物多样性研究的热点之一。以往研究中一般将山体划分为等海拔间距的高度带, 以分析物种丰富度的垂直格局, 其缺陷在于因各高度带面积不相等而可比性下降。为消除面积不相等的影响, 作者利用数字高程数据(DEM, Digital Elevation Model)在地理信息系统(GIS)工具支持下, 尝试将贺兰山(海拔范围1,300–3,500 m)划分为等面积的数个高度带, 从而分析其物种丰富度的海拔格局。结果表明: (1) 贺兰山物种丰富度呈现为单峰式海拔格局, 峰值出现在海拔2,000 m附近。(2) 逐步回归分析显示, 坡度异质性是解释物种丰富度海拔分布格局的最优因子。高度带的坡度异质性越大, 意味着地形的起伏变化越大, 反映出生境类型越趋多样化, 从而可维持多个物种的共存。(3) 贺兰山植物物种丰富度在海拔2,000 m 附近达到峰值, 可能与植被演变历史、气候条件、地形复杂度、生态过渡带和中间膨胀效应的共同影响有关。(4) 对山体进行等面积划带, 可直接消除面积不相等带来的影响, 与等间距划带的方法相比, 尤其在物种海拔分布信息准确度较高时更具优势。     

神农架自然保护区非飞行哺乳动物的物种丰富度:沿海拔梯度的分布格局

于1999～2001年调查了神农架自然保护区6个地点不同栖息地的非飞行哺乳动物的物种丰富度。栖息地分为8类：原始林、择伐林（采伐枯立木）、次生林、灌木林、草地、常年性河流水溪、农田和人居住区。小型非飞行哺乳动物调查用捕鼠夹;大型非飞行哺乳动物调查主要根据皮张收购资料以及样线法和痕迹法;用10 m×10 m的样方调查林地树种丰富度。调查发现,神农架自然保护区有非飞行哺乳动物59种［不包括引进种梅花鹿（Cervus nippon）］。在同一海拔高度,原始林通常比择伐林和次生林的物种丰富度高,说明采伐严重降低了物种丰富度。对比同一栖息地不同海拔高度的物种丰富度,我们发现,在中海拔地段（800～1700 m）物种丰富度最高：如在原始林和次生林,海拔1700 m的东溪物种丰富度最高;在择伐林,海拔800 m的九冲物种丰富度最高。聚类分析显示,6个地点的哺乳动物物种组成可以分为两组：高海拔组（2100 m以上）和中低海拔组（1700 m以下）。各地点的哺乳动物物种组成与植被的垂直分布是一致的。各地点的物种丰富度与单位面积（100 m²）树种平均丰富度、栖息地类型数和海拔高度相关。3个环境变量间也是相关的：海拔高度对单位面积树种平均丰富度和栖息地类型数有重要影响。根据研究结果提出两点保护建议：第一,保护区的移民迁出和退耕还林工程应首先在物种丰富度最高的九冲进行,而后是东溪和下谷;第二,为了增加个体流和基因流,保护区东西两片相间的非保护区地带应划入保护区,建立栖息地廊道。     

基于红外相机监测的广东南岭国家级自然保护区鸟兽多样性及其垂直分布特征

生物多样性的海拔格局一直是生态学、生物地理学和保护生物学研究的核心问题之一。本研究利用红外相机对广东南岭国家级自然保护区完整垂直带的兽类和鸟类开展连续10年的野外监测,分析了保护区当前鸟兽多样性及受胁情况,并通过整合水平与垂直分布的多样性格局开展热点与空缺分析。2012–2021年间共设置了116个红外相机点位,相机累计拍摄85,164个工作日,获得可识别独立有效照片21,194张,共记录到兽类24种,鸟类50种。兽类受威胁物种比例较高,为45.83%。相对多度指数(relative abundance index, RAI)最高的5种兽类为赤麂(Muntiacus vaginalis)、小麂(M. reevesi)、红腿长吻松鼠(Dremomys pyrrhomerus)、鼬獾(Melogale moschata)和藏酋猴(Macaca thibetana);而红颊獴(Herpestes javanicus)和水鹿(Rusa unicolor) RAI最低,仅各拍摄到1次。RAI最高的4种鸟类是白鹇(Lophuranycthemera)、紫啸鸫(Myophonuscaeruleus)...     

物种丰富度垂直分布格局及影响机制

物种丰富度分布格局是一定地域内物种丰富度沿三维空间的立体分布,包括物种丰富度在经度、纬度和垂直梯度(海拔高度和海水深度)三个维度上的空间分异。近年来物种多样性的垂直分布格局与机制研究得到了生物地理学家和生态学家的重视。物种丰富度的垂直分布格局存在多种类型,但随海拔增加而物种数减少的单调递减模型和中海拔物种丰富度最高的单峰模型较为常见。目前在机制研究中验证较多的是气候稳定性、生物因子(种间相互作用)、能量、生境异质性、干扰、进化时间、物种分化速率、面积、中域效应(mid-domain effect)、生态位保守性(niche conservatism)等假说和机制。物种丰富度的分布格局是多方面因素综合作用的结果;由于地理、地形、气候、地质演化历史、物种库和进化历史、物种分化速率、干扰等差异,在不同地区存在着特别的物种丰富度空间分布格局和机制;处于同一地区的不同类群的物种也因进化扩散历史和生态适应能力不同而呈现多样化的分布格局。因此,对不同地区和类群的物种丰富度格局和机制进行研究应具体分析后才能得到可信结论。     

Rotifer species richness along an altitudinal gradient in the Alps

Aim Biodiversity patterns along altitudinal gradients are less studied in aquatic than terrestrial systems, even though aquatic sites provide a more homogeneous environment independent of moisture constraints. We studied the altitudinal species richness pattern for planktonic rotifers in freshwater lakes and identified the environmental predictors for which altitude is a proxy. Location Two hundred and eighteen lakes of Trentino–South Tyrol (Italy) in the eastern Alps; lakes covered 98% (range 65–2960 m above sea level) of the altitudinal gradient in the Alps. Methods We performed: (1) linear regression between species richness and altitude to evaluate the general pattern, (2) multiple linear regression between species richness and environmental predictors excluding altitude to identify the most important predictors, and (3) linear regression between the residuals of the best model of step (2) and altitude to investigate any additional explanatory power of altitude. Selection of environmental predictors was based on limnological importance and non‐parametric Spearman correlations. We applied ordinary least squares regression, generalized linear, and generalized least squares modelling to select the most statistically appropriate model. Results Rotifer species richness showed a monotonic decrease with altitude independent of scale effects. Species richness could be explained (R²= 51%) by lake area as a proxy for habitat diversity, reactive silica and total phosphorus as proxies for productivity, water temperature as a proxy for energy, nitrate as a proxy for human influence and north–south and east–west directions as covariates. These predictors completely accounted for the species richness–altitude pattern, and altitude had no additional effect on species richness. Main conclusions The linear decrease of species richness along the altitudinal gradient was related to the interplay of habitat diversity, productivity, heat content and human influence. These factors are the same in terrestrial and aquatic habitats, but the greater environmental stability of aquatic systems seems to favour a linear pattern.     

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。     

Plant species richness and diversity along an altitudinal gradient in the Sierra Nevada, Mexico

This article presents an analysis of plant species richness and diversity and its association with climatic and soil variables along a 1300‐m elevation gradient on the Cerro Tláloc Mountain in the northern Sierra Nevada in Mexico. Two 1000‐m² tree sampling plots were created at each of 21 selected sampling sites, as well as two 250‐m² plots for shrubs and six 9‐m² plots for herbaceous plants. Species richness and diversity were estimated for each plant life form, and beta diversity between sites was estimated along the gradient. The relationship between species richness and diversity and environmental variables was modelled using simple linear correlation and regression trees. Species richness and diversity showed a unimodal pattern with a bias towards high values in the lower half of the elevation gradient under study. This response was consistent for all three life forms. Beta diversity increased steadily along the elevation gradient, being lower between contiguous sites at intermediate elevations and high – the species replacement rate was nearly 100%– between sites at the extremes of the gradient. Few species were adapted to the full spectrum of environmental variation along the elevation gradient studied. The regression tree suggests that differences in species richness are mainly influenced by elevation (temperature and humidity) and soil variables, namely A₂ permanent wilting point, organic matter and horizon field capacity and A₁ horizon Mg²⁺.     

Short-term variation in species richness across an altitudinal gradient of alpine summits

In response to climate warming, high altitude alpine vegetation may be replaced by typically lower altitude species, as species re-assemble and migrate to new areas. However, empirical evidence showing vegetation change in response to climate warming is largely unavailable for Australian alpine areas. Here, we examine changes in species richness with respect to climate and altitude over a 7?year period at a range of spatial scales in a re-survey of five alpine summits that are part of the Global Observation Research Initiative in Alpine Environments monitoring network. Eighty species were recorded in 2011 across all summits, an increase of 6 species since 2004. Mean species richness increased at the whole-of-summit scale from 45 to 50 species (about 12?%). At this scale, the rate of species richness increase was almost one new species per year, with 15 new species recorded at one summit. Here, shrub and graminoid species showed the largest increases. At the smaller spatial scales, changes in species richness were less pronounced. Turnover at the species and community level was typically moderate at all spatial scales and on all summits. The strength and direction of species richness change (the difference in species richness between the two sample periods, +/?) was not related to altitude nor variation in climate. Future re-surveys of the summits will confirm whether these short-term variations in species richness, particularly increases in shrubs, are indeed signals of longer-term trends and interactions with a changing climate.     

Leaf size zonation pattern of woody species along an altitudinal gradient on Mt. Pulog,Philippines

Leaf size zonation along an altitudinal gradient from 2000–2700 m a.s.l. on Mt. Pulog, Cordillera mountain range, Luzon Is., Philippines was examined using the Raunkiaer-Webb classification system. The entire altitudinal range studied was dominated by the small leaf size classes which possess thick, lustrous, pubescent leaves adapted to high evapotranspiration, cold temperature and other stressful conditions. Altitudinal leaf size zonation was identified as follows: (1) pure needle leaved zone from 2000–2300 m a.s.l., (2) mixed needle leaved/microphyllous zone from 2300–2400 m a.s.l., (3) microphyllous zone from 2400–2600 m a.s.l. and, (4) microphyllous/nanophyllous zone from 2600–2700 m a.s.l., coinciding with the altitudinal vegetation zonation. This pattern is different from that in other tropical mountains, which usually show a gradual shift from a mesophyllous zone in the lowland to a nanophyllous zone in the upper subalpine. Stressful conditions such as steep topography (1200–2300 m a.s.l.), cloud cover, decrease of temperature, strong winds (2600–2700 m a.s.l.) could have influenced the altitudinal leaf size zonation on Mt. Pulog. The complex phytogeographical position of Mt. Pulog as a transition region between the tropics and subtropics have also influenced leaf size zonation as in eastern Himalaya, southwestern China and Taiwan.     

Species richness and trait composition of butterfly assemblages change along an altitudinal gradient

Species richness patterns along altitudinal gradients are well-documented ecological phenomena, yet very little data are available on how environmental filtering processes influence the composition and traits of butterfly assemblages at high altitudes. We have studied the diversity patterns of butterfly species at 34 sites along an altitudinal gradient ranging from 600 to 2,000 m a.s.l. in the National Park Berchtesgaden (Germany) and analysed traits of butterfly assemblages associated with dispersal capacity, reproductive strategies and developmental time from lowlands to highlands, including phylogenetic analyses. We found a linear decline in butterfly species richness along the altitudinal gradient, but the phylogenetic relatedness of the butterfly assemblages did not increase with altitude. Compared to butterfly assemblages at lower altitudes, those at higher altitudes were composed of species with larger wings (on average 9 %) which laid an average of 68 % more eggs. In contrast, egg maturation time in butterfly assemblages decreased by about 22 % along the altitudinal gradient. Further, butterfly assemblages at higher altitudes were increasingly dominated by less widespread species. Based on our abundance data, but not on data in the literature, population density increased with altitude, suggesting a reversed density–distribution relationship, with higher population densities of habitat specialists in harsh environments. In conclusion, our data provide evidence for significant shifts in the composition of butterfly assemblages and for the dominance of different traits along the altitudinal gradient. In our study, these changes were mainly driven by environmental factors, whereas phylogenetic filtering played a minor role along the studied altitudinal range.     

不同经度天山云杉群落物种丰富度随海拔梯度变化

选择我国新疆境内天山山脉81°05′—93°415′E约12 个经度范围的昭苏、巩留、乌苏、乌鲁木齐和哈密5 个地点的天山云杉林进行垂直样带调查,分析不同经度位置天山云杉群落物种丰富度随海拔梯度的变化.结果表明：各经度的天山云杉群落是以天山云杉为优势树种的纯林,乔木和灌木种类很少,草本植物的物种丰富度主要由优势树种天山云杉控制.天山云杉在中等海拔范围分布最集中、郁闭度最大、生长最好、蓄积量最高,致使林下草本植物的物种丰富度最低.天山云杉群落草本物种丰富度随海拔梯度的变化呈山谷型曲线,可以用二次曲线方程y=ax²-bx+c(a,b,c＞0)进行描述.     

Carbon assimilation,nitrogen, and photochemical efficiency of different Himalayan tree species along an altitudinal gradient

In the area of Jumla region in Western Nepal, measurements of saturated leaf net photosynthetic rate (P_sat), nitrogen content, leaf fluorescence, carbon isotopic composition, and water status were performed on woody coniferous (Pinus wallichiana, Picea smithiana, Abies spectabilis, Juniperus wallichiana, Taxus baccata), evergreen (Quercus semecarpifolia, Rhododendron campanulatum), and deciduous broadleaved species (Betula utilis, Populus ciliata, Sorbus cuspidata) spreading from 2 400 m up to the treeline at 4 200 m a.s.l. With the exception of J. wallichiana, P_sat values were lower in coniferous than broadleaved species. Q. semecarpifolia, that in this area grows above the coniferous belt between 3 000 and 4 000 m, showed the highest P_sat at saturating irradiance and the highest leaf N content. This N content was higher and P_sat lower than those of evergreen oak species of tempe forests at middle and low altitudes. For all species, P_sat and N content were linearly correlated, but instantaneous nitrogen use efficiency was lower than values measured in lowland and temperate plant communities. The values of carbon isotopic composition, estimated by δ₁₃C, showed the same range reported for temperate tree species. The ranking of δ₁₃C values for the different tree types was conifers < evergreen broadleaved<deciduous, suggesting tighter stomatal closure and higher water use efficiency for the evergreen types, confirming trends found elsewhere. No relevant differences of δ₁₃C were found along the altitudinal gradient. Quantum yield of photochemistry at saturating irradiance, measured by leaf fluorescence (δF/F_m’), was highest in J. wallichiana and lowest in T. baccata. Overall, photochemical efficiency was more strongly related to species than to altitude. Interestingly, changes of .δF/F_m’ along the altitudinal gradient correlated well with the reported altitudinal distribution of the species.     

Constant tree species richness along an elevational gradient of Mt. Bokor,a table-shaped mountain in southwestern Cambodia

Some previous studies along an elevational gradient on a tropical mountain documented that plant species richness decreases with increasing elevation. However, most of studies did not attempt to standardize the amount of sampling effort. In this paper, we employed a standardized sampling effort to study tree species richness along an elevational gradient on Mt. Bokor, a table-shaped mountain in southwestern Cambodia, and examined relationships between tree species richness and environmental factors. We used two methods to record tree species richness: first, we recorded trees taller than 4 m in 20 uniform plots (5 × 100 m) placed at 266–1048-m elevation; and second, we collected specimens along an elevational gradient from 200 to 1048 m. For both datasets, we applied rarefaction and a Chao1 estimator to standardize the sampling efforts. A generalized linear model (GLM) was used to test the relationship of species richness with elevation. We recorded 308 tree species from 20 plots and 389 tree species from the general collections. Species richness observed in 20 plots had a weak but non-significant correlation with elevation. Species richness estimated by rarefaction or Chao1 from both data sets also showed no significant correlations with elevation. Unlike many previous studies, tree species richness was nearly constant along the elevational gradient of Mt. Bokor where temperature and precipitation are expected to vary. We suggest that the table-shaped landscape of Mt. Bokor, where elevational interval areas do not significantly change between 200 and 900 m, may be a determinant of this constant species richness.