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1.
1. Despite the growing view that biodiversity provides a unifying theme in river ecology, global perspectives on richness in riverine landscapes are limited. As a result, there is little theory or quantitative data on features that might have influenced global patterns in riverine richness, nor are there clear indications of which riverine landscapes are important to conservation at the global scale. As conspicuous elements of the vertebrate fauna of riverine landscapes, we mapped the global distributions of all of the world's specialist riverine birds and assessed their richness in relation to latitude, altitude, primary productivity and geomorphological complexity (surface configuration). 2. Specialist riverine birds, typical of high‐energy riverine landscapes and dependent wholly or partly on production from river ecosystems, occur in 16 families. They are represented by an estimated 60 species divided equally between the passerines and non‐passerines. Major radiation has occurred among different families on different continents, indicating that birds have evolved several times into the niches provided by riverine landscapes. 3. Continental richness varies from four species in Europe to 28 in Asia, with richness on the latter continent disproportionately larger than would be expected from a random distribution with respect to land area. Richness is greatest in mountainous regions at latitudes of 20–40°N in the riverine landscapes of the Himalayan mountains, where 13 species overlap in range. 4. Family, genus and species richness in specialist riverine birds all increase significantly with productivity and surface configuration (i.e. relief). However, family richness was the best single predictor of the numbers of species or genera. In keeping with the effect of surface configuration, river‐bird richness peaks globally at 1300–1400 m altitude, and most species occur typically on small, fast rivers where they feed predominantly on invertebrates. Increased lengths of such streams in areas of high relief and rainfall might have been responsible for species–area effects. 5. We propose the hypothesis that the diversity in channel forms and habitats in riverine landscapes, in addition to high temperature and primary productivity, have been prerequisites to the development of global patterns in the richness of specialist riverine organisms. We advocate tests of this hypothesis in other taxonomic groups. We draw attention, however, to the challenges of categorically defining riverine organisms in such tests because (i) rivers grade into many other habitat types across several different ecotones and (ii) `terrestrialisation' processes in riverine landscapes means that they offer habitat for organisms whose evolutionary origins are not exclusively riverine.  相似文献   

2.
The combined effects of scale and productivity on species richness   总被引:4,自引:1,他引:4  
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3.
高寒草甸不同草地群落物种多样性与生产力关系研究   总被引:30,自引:3,他引:30  
生态系统的结构和功能、生物多样性与生产力的关系问题是近年来群落生态学中研究的中心问题,其中,生态系统生产力水平是其功能的重要表现形式,用4种不同草地类型探讨自然群落的物种多样性与生产力关系.结果表明,矮嵩草草甸、小嵩草草甸和金露梅灌丛群落中物种多样性与生产力的关系呈线性增加关系,藏嵩草沼泽化草甸群落中线性增加关系不显著,这表明群落生产力除受物种多样性的影响外,也受物种本身特征和环境资源的影响.不同的环境资源和环境异质性是形成群落结构特征、物种多样性分布格局差异的主要原因之一.  相似文献   

4.

Aim

To demonstrate a new and more general model of the species–area relationship that builds on traditional models, but includes the provision that richness may vary independently of island area on relatively small islands (the small island effect).

Location

We analysed species–area patterns for a broad diversity of insular biotas from aquatic and terrestrial archipelagoes.

Methods

We used breakpoint or piecewise regression methods by adding an additional term (the breakpoint transformation) to traditional species–area models. The resultant, more general, species–area model has three readily interpretable, biologically relevant parameters: (1) the upper limit of the small island effect (SIE), (2) an estimate of richness for relatively small islands and (3) the slope of the species–area relationship (in semi‐log or log–log space) for relatively large islands.

Results

The SIE, albeit of varying magnitude depending on the biotas in question, appeared to be a relatively common feature of the data sets we studied. The upper limit of the SIE tended to be highest for species groups with relatively high resource requirements and low dispersal abilities, and for biotas of more isolated archipelagoes.

Main conclusions

The breakpoint species–area model can be used to test for the significance, and to explore patterns of variation in small island effects, and to estimate slopes of the species–area (semi‐log or log–log) relationship after adjusting for SIE. Moreover, the breakpoint species–area model can be expanded to investigate three fundamentally different realms of the species–area relationship: (1) small islands where species richness varies independent of area, but with idiosyncratic differences among islands and with catastrophic events such as hurricanes, (2) islands beyond the upper limit of SIE where richness varies in a more deterministic and predictable manner with island area and associated, ecological factors and (3) islands large enough to provide the internal geographical isolation (large rivers, mountains and other barriers within islands) necessary for in situ speciation.
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5.
A highly diverse T-cell receptor (TCR) repertoire is a fundamental property of an effective immune system, and is associated with efficient control of viral infections and other pathogens. However, direct measurement of total TCR diversity is impossible. The diversity is high and the frequency distribution of individual TCRs is heavily skewed; the diversity therefore cannot be captured in a blood sample. Consequently, estimators of the total number of TCR clonotypes that are present in the individual, in addition to those observed, are essential. This is analogous to the ‘unseen species problem’ in ecology. We review the diversity (species richness) estimators that have been applied to T-cell repertoires and the methods used to validate these estimators. We show that existing approaches have significant shortcomings, and frequently underestimate true TCR diversity. We highlight our recently developed estimator, DivE, which can accurately estimate diversity across a range of immunological and biological systems.  相似文献   

6.
The total number of insect species in the world is an important if elusive figure. We use a fresh approach to estimate global insect species richness, based on biogeographic patterns of diversity of well or better documented taxa. Estimates generated by various calculations, all variations on a theme, largely serve to substantiate suggestions that insect species are likely to number around 10 million or less.  相似文献   

7.
The North American woody species, Prunus serotina Ehrh., is an aggressive invader of forest understories in Europe. To better understand the plant invasion process, we assessed understorey plants and Prunus serotina seedlings that have colonized a 35-year-old replicated common-garden experiment of 14 tree species in south-western Poland. The density and size of established (> 1 year old) P. serotina seedlings varied among overstorey species and were related to variation in light availability and attributes of the understorey layer. In a multiple regression analysis, the density of established P. serotina seedlings was positively correlated with light availability and understorey species richness and negatively correlated with understorey species cover. These results suggest that woody invader success is adversely affected by overstorey shading and understorey competition for resources. Simultaneously, however, invader success may generally be positively associated with understorey species richness because both native and invasive plant colonization respond similarly to environmental conditions, including those influenced by overstorey tree species. Identification of characteristics of forests that increase their susceptibility to invasion may allow managers to target efforts to detect invasives and to restore forests to states that may be less invasible.  相似文献   

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Taylor  Andy F. S. 《Plant and Soil》2002,244(1-2):19-28
A number of recent review articles on ectomycorrhizal (ECM) fungal community diversity have highlighted the unprecedented increase in the number of publications on this ecologically important but neglected area. The general features of these species-rich, highly dynamic and complex communities have been comprehensively covered but one aspect crucial to our assessment of diversity, namely the sampling of ECM communities has received less attention. This is a complex issue with two principal components, the physical sampling strategy employed and the life cycle traits of the ECM fungi being examined. Combined, these two components provide the image that we perceive as ECM diversity. This contribution will focus primarily on the former of these components using a recent study from a pine forest in central Sweden to highlight some sampling problems and also to discuss some features common to ECM communities. The two commonly used elements of diversity, species richness and community evenness, present rather different problems in the assessment of ECM diversity. The applicability of using current measures of abundance (number or percentage of root tips colonised) to determine community evenness is discussed in relation to our lack of knowledge on the size of individual genets of ECM fungi. The inherent structure of most ECM communities, with a few common species and a large number of rare species, severely limits our ability to accurately assess species richness. A discussion of theoretical detection limits is included that demonstrates the importance of the sampling effort (no. of samples or tips) involved in assessing species richness. Species area abundance plots are also discussed in this context. It is suggested that sampling strategy (bulk samples versus multiple collections of single tips) may have important consequences when sampling from communities where root tip densities differ. Finally, the need for studies of the spatial distribution of ECM on roots in relation to small-scale soil heterogeneity and of the temporal aspects of ECM community dynamics is raised.  相似文献   

11.
The communities of Larix chinensis and their ecotone in Qinling Mountains were investigated by sampling belt method. Species richness, Simpson diversity, Shannon-Weiner diversity, PIE and Pielou evenness indices of vascular plants in their communities and ecotone were calculated. Structure and composition of the communities in 6 sampling belts within the sites were analyzed. The results showed that the edge effect was obvious in the ecotone with a less changing environment (such as soil and terrain) and acute variation of composition and structure, while inconspicuous or even none in the ecotone with worse environmental condition (such as great space fluctuation). It is apparent that the edge effect of community was affected by soil and terrain, but not by microclimate. __________ Translated from Guibaia, 2005, 25 (2)[译自: 广西植物, 2005,25(2)]  相似文献   

12.
The process of forest fragmentation, a common phenomenon occurring in tropical forests, not only results into continuously forest getting fragmented but also brings about several physical and biological changes in the environment of forests. Consequently, there is a loss of biodiversity due to change in habitat conditions. These remnant fragments provide the last hope for biodiversity conservation. The present study deals with the impact of decreasing patch size of a fragmented forest on the diversity of the tropical dry deciduous forests in Vindhyan highlands, India. There is considerable change in the vegetation cover of this region owing to rapid industrialization and urbanization, which has also contributed to forest fragmentation. In the present study, remotely sensed data has been used to describe the changes brought about in vegetated areas over a period of 10 years as a result of fragmentation and its impact on biodiversity was assessed. Further, in order to assess the loss of species with respect to the reduction in patch size, species area curves for various change areas were analysed. It was observed that the rate of decrease in the number of species is faster in the case of negative change areas as compared to the positive change areas of the region. Various diversity indices also support this observation. Such an analysis would help in formulating appropriate conservation measures for the region.  相似文献   

13.
This paper concludes a collection of contributions presented at the 8th Workshop of the International Association of Phytoplankton Taxonomy and Ecology. It derives a consensus as to the virtues and strengths of J. H. Connell's Intermediate Disturbance Hypothesis (IDH), its applicability to phytoplankton ecology and its theoretical and practical weaknesses. The view is expressed that the IDH is too useful a concept to reject and that, as a word model, it provides a powerful link between diversity and disturbance. The more robust investigations that are necessary to consolidate the tenancy of IDH need to concentrate upon the separation and quantification of the stimulus- and response-components of disturbance.  相似文献   

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不同更新方式对林地植物群落特种多样性的影响   总被引:1,自引:0,他引:1  
本文就人工林经营中的三种更新方式对植物群落中物种多样性的影响进行研究。结果表明,1200m^2样地物种丰富度为:天然更新159种,人促更新130种,人工造林94种;多样性指数(Dsh)分别为4.3004、3.9283、3.5048;多样性均匀度指数(Jsh)分别为0.8484、0.8070、0.7714。人工造林的营林干扰是物种丧失和林分物种多样性下降的主要原因。  相似文献   

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应用指示种预测森林管理对物种多样性及群落组成的影响   总被引:2,自引:0,他引:2  
采用指示种分析方法,研究了会同亚热带森林物种多样性和群落组成对森林管理的响应.从357个林下种中鉴定出显著性指示种94个,并构造新的指示种数据集,检验指示种数据集和源群落数据集之间的关联,评估指示种对林下植被管理效应的预测潜能.结果表明:指示种数据集和源群落数据集之间存在极显著的关联(Mantel r=0.898),指示种数据集很好地预测了生物多样性的变化(回归分析,R2>0.74);指示种很好地预测了群落组成对森林管理的响应(ANOVA,F>16.79);非度量多尺度排序(NMDS)以及K-means聚类分析表明,对于不同森林管理的样地类型,指示种数据集的识别能力和源群落数据集是一致的.从物种多样性、群落组成以及在森林类型的识别上,指示种数据集和源群落数据集有一致性规律,作用几乎相同,因此森林评估可以利用指示种代替源群落预测森林管理效应,以减少森林全面调查的成本.  相似文献   

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