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1.
The diversity of ecological communities has been the focus of many studies. Because biodiversity provides several indicators used in an Ecosystem Approach to Fisheries (EAF) to track changes in fish communities, we investigated the spatial and temporal patterns in the diversity of some demersal fish communities subjected to varying fishing pressure. Depth and catch rate were the most important predictors in explaining changes in diversity followed by longitude and survey year. Diversity, as measured by the various indices except for taxonomic distinctness (∆*), initially declined with increasing depth to about a depth of 80 m, then increased to about 150 m after which it declined. Taxonomic distinctness index (∆*) showed an increase in the taxonomic heterogeneity of the demersal community below the 300-m isobath. Diversity remained relatively constant with increase in longitude to around 24°E (which has the lowest diversity) after which it increased. The assessment of the temporal trend in diversity indicates that survey year has a significant effect on all diversity indices except for ∆*. Diversity increased and dominance declined with time. This may be result of a decline in the abundance of dominant species or an increase in the abundance less dominant species, or a combination of both effects. Multivariate analysis of the set of diversity indices showed three groups of indices: those reflecting species richness (S, Margalef’s d), those measuring mainly taxonomic relatedness (∆*), and those balancing the richness and evenness components of diversity (J′, H′, λ, ∆, Hill’s N1, and Hill’s N2). The relationship between evenness, catch rate, and size was also investigated. Size classes with highest evenness were found to have lowest catch rate and vice versa. This highlights the need to consider the size and trophic level of species when linking diversity to the functioning of ecosystems.  相似文献   

2.
Little is known about the biodiversity of free-living nematodes. We have attempted to provide baseline information about the natural diversities (those not influenced by pollution) that might be expected in six biotopes. Seventeen marine nematode data sets consisting of 197 samples were standardized to allow a comparison of alpha diversity, or sample diversity, from temperate estuarine, tropical sublittoral, temperate sublittoral, bathyal, abyssal, and hadal biotopes, which were selected on criteria of depth and latitude. The diversity analysis methods we employed were rarefaction curves; three weighted diversity indices of species richness, SR, H', and ES(X); and two equitability indices, J' and V. Diversity was significantly different in the six biotopes. The weighted indices of species richness were more capable of resolving differences between the biotopes than were the equitability indices, whose large standard errors suggested that they were more influenced by local, small-scale ecological factors. This suggests that species richness is a better measure than equitability for large-scale comparisons of biotopes or regions. The ES(X), which is robust to sample size variations, was more efficient than the weighted indices of species richness, which were easily influenced by sample size. There was a nonlinear relationship between depth and diversity with the bathyal and abyssal biotopes displaying the highest diversity. The tropical sublittoral biotope was not more diverse than the temperate sublittoral biotope. The lowest diversities were found in the physically challenging temperate estuarine and hadal biotopes.  相似文献   

3.
Ecological theory and current evidence support the validity of various species response curves according to a variety of environmental gradients. Various methods have been developed for building species distribution models but it is not well known how these methods perform under various assumptions about the form of the underlying species response. It is also not well known how spatial correlation in species occurrence affects model performance. These effects were investigated by applying an environmental envelope method (BIOCLIM) and three regression-based methods: logistic regression (LR), generalized additive modelling (GAM), and classification and regression tree (CART) to simulated species occurrence data. Each simulated species was constructed as a sum of responses with varying weights. Three basic species response curves were assumed: Gaussian (bell-shaped), Beta (skew) and linear. The two non-linear responses conform to standard ecological niche theory. All three responses were applied in turn to three simulated environmental variables, each with varying degrees of spatial autocorrelation. GAM produced the most consistent model performance over all forms of simulated species response. BIOCLIM and CART were inclined to underrate the performance of variables with a linear response. BIOCLIM was less sensitive to data density. LR was susceptible to model misspecification. The use of a linear function in LR underestimated the performance of variables with non-linear species response and contributed to increased spatial autocorrelation in model residuals. Omission of important environmental variables with non-linear species response also contributed to increased spatial autocorrelation in model residuals. Adding a spatial autocovariate term to the LR model (autologistic model) reduced the spatial autocorrelation and improved model performance, but did not correct the misidentification of the dominant environmental determinant. This is to be expected since the autologistic approach was designed primarily for prediction and not for inference. Given that various forms of species response to environmental determinants arise commonly in nature: (1) higher order functions should always be tested when applying LR in modelling species distribution; (2) spatial autocorrelation in species distribution model residuals can indicate that environmental determinants with non-linear response are missing from the model; and (3) deficiencies in LR model performance due to model misspecification can be addressed by adding a spatial autocovariate to the model, but care should be taken when interpreting the coefficients of the model parameters.  相似文献   

4.
A link between ecological diversity indices and measures of biodiversity   总被引:1,自引:0,他引:1  
The practice of environmental planning and protection frequently necessitates the quantification of ecological diversity. Traditional ‘ecological diversity indices’ are based on the abundances of species present. However, such indices are insensitive to taxonomic or similar differences. With equal species abundances they measure the species richness (species number) only. Conversely, so-called ‘biodiversity indices’ are based on species differences, but are insensitive to the abundance conditions. The quadratic entropy index is the only ecological diversity index, the value of which reflects both the differences ‘and’ abundances of the species. When a species list is given without abundance data, then, using the quadratic entropy index and postulating equal abundances, one gets the only biodiversity index derived from a traditional ecological index of diversity. Its extensive form is identical with the sum of differences or distances between the species present. This index trivially satisfies set monotonicity, an important property for biodiversity indices.  相似文献   

5.
Bock CE  Jones ZF  Bock JH 《Ecology》2007,88(5):1322-1327
Species richness and evenness are components of biological diversity that may or may not be correlated with one another and with patterns of species abundance. We compared these attributes among flowering plants, grasshoppers, butterflies, lizards, summer birds, winter birds, and rodents across 48 plots in the grasslands and mesquite-oak savannas of southeastern Arizona. Species richness and evenness were uncorrelated or weakly negatively correlated for each taxonomic group, supporting the conclusion that richness alone is an incomplete measure of diversity. In each case, richness was positively correlated with one or more measures of abundance. By contrast, evenness usually was negatively correlated with the abundance variables, reflecting the fact that plots with high evenness generally were those where all species present were about equally uncommon. Therefore richness, but not evenness, usually was a positive predictor of places of conservation value, if these are defined as places where species of interest are especially abundant. Species diversity was more positively correlated with evenness than with richness among grasshoppers and flowering plants, in contrast to the other taxonomic groups, and the positive correlations between richness and abundance were comparatively weak for grasshoppers and plants as well. Both of these differences can be attributed to the fact that assemblages of plants and grasshoppers were numerically dominated by small subsets of common species (grasses and certain spur-throated grasshoppers) whose abundances differed greatly among plots in ways unrelated to species richness of the groups as a whole.  相似文献   

6.
以89个植物群落调查样地数据为基础,运用8个多样性指数对山西关帝山神尾沟物种多样性与环境之间的关系进行了分析.(1)群落总的表现为多样性和均匀度随海拔升高而下降,丰富度从1700m下降到2400m后开始升高;(2)群落不同层次表现为乔木层和灌木层多样性、丰富度和均匀度随海拔升高而下降,草本多样性和均匀度表现为上升趋势,丰富度下降到1900m后开始上升;(3)乔灌草三者多样性和丰富度指数值以及变化幅度都表现为草本层>灌木层>乔木层,三者均匀度相差不大;(4)群落不同坡向表现为阳坡多样性和丰富度都大于阴坡,均匀度相差不大.图6参7  相似文献   

7.
威海市区黑松林群落的物种多样性特征   总被引:3,自引:1,他引:2  
用3个丰富度指数、2个多样性指数和3个均匀度指数对威海市区11个黑松林群落多样性进行研究,并用相关分析研究了这些指数间的关系,结果表明:(1)黑松混交林群落的丰富度和多样性均高于黑松纯林群落,但均匀度却无此规律;(2)生境最优的黑松+刺槐+麻栎林(位于仙姑顶的样地11)在11个样地中的物种多样性表现最好,丰富度、多样性和均匀度都最大.而生境最差的位于火炬大厦的黑松纯林(样地2)群落的丰富度和多样性指数都最小;(3)除样地2外,其余样地群落的草本层丰富度和多样性都最大,灌木层次之,乔木层最小,均匀度无此规律;(4)3个丰富度指数之间、2个多样性指数之间以及两个Pielou均匀度指数之间存在极显著的相关性,但Alatalo均匀度指数和其它7个指数之间相关性都不显著,同时对8个物种多样性指数进行比较后发现丰富度指数中Patrick指数(S)最优,而多样性指数中Shannon-Wiener(H)最优,均匀度指数中以H为基础计算出的Pielou(JH)指数最优.  相似文献   

8.
Forest conversion is one of the greatest global threats to biodiversity, and land-use change and subsequent biodiversity declines sometimes occur over a variety of underlying geologies. However, how forest conversion and underlying geology interact to alter biodiversity is underappreciated, although spatial variability in geology is considered an integral part of sustaining ecosystems. We aimed to examine the effects of forest conversion to farmland, the underlying geology, and their interaction on the stream fishes’ diversity, evenness, and abundance in northeastern Japan. We disentangled complex pathways between abiotic and biotic factors with structural equation modeling. Species diversity of stream fishes was indirectly shaped by the interaction of land use and underlying geology. Diversity declined due to nutrient enrichment associated with farmlands, which was mainly the result of changes in evenness rather than by changes in species richness. This impact was strongest in streams with volcanic geology with coarse substrates probably because of the differential responses of abundant stream fishes to nutrient enrichment (i.e., dominance) and the high dependency of these fishes on large streambed materials during their life cycles. Our findings suggest that remediation of deforested or degraded forest landscapes would be more efficient if the interaction between land use and underlying geology was considered. For example, the negative impacts of farmland on evenness were larger in streams with volcanic geology than in other stream types, suggesting that riparian forest restoration along such streams would efficiently provide restoration benefits to stream fishes. Our results also suggest that land clearing around such streams should be avoided to conserve species evenness of stream fishes.  相似文献   

9.
Villéger S  Mason NW  Mouillot D 《Ecology》2008,89(8):2290-2301
Functional diversity is increasingly identified as an important driver of ecosystem functioning. Various indices have been proposed to measure the functional diversity of a community, but there is still no consensus on which are most suitable. Indeed, none of the existing indices meets all the criteria required for general use. The main criteria are that they must be designed to deal with several traits, take into account abundances, and measure all the facets of functional diversity. Here we propose three indices to quantify each facet of functional diversity for a community with species distributed in a multidimensional functional space: functional richness (volume of the functional space occupied by the community), functional evenness (regularity of the distribution of abundance in this volume), and functional divergence (divergence in the distribution of abundance in this volume). Functional richness is estimated using the existing convex hull volume index. The new functional evenness index is based on the minimum spanning tree which links all the species in the multidimensional functional space. Then this new index quantifies the regularity with which species abundances are distributed along the spanning tree. Functional divergence is measured using a novel index which quantifies how species diverge in their distances (weighted by their abundance) from the center of gravity in the functional space. We show that none of the indices meets all the criteria required for a functional diversity index, but instead we show that the set of three complementary indices meets these criteria. Through simulations of artificial data sets, we demonstrate that functional divergence and functional evenness are independent of species richness and that the three functional diversity indices are independent of each other. Overall, our study suggests that decomposition of functional diversity into its three primary components provides a meaningful framework for its quantification and for the classification of existing functional diversity indices. This decomposition has the potential to shed light on the role of biodiversity on ecosystem functioning and on the influence of biotic and abiotic filters on the structure of species communities. Finally, we propose a general framework for applying these three functional diversity indices.  相似文献   

10.
Meynard CN  Quinn JF 《Ecology》2008,89(4):981-990
Spatial structure in metacommunities and their relationships to environmental gradients have been linked to opposing theories of community assembly. In particular, while the species sorting hypothesis predicts strong environmental influences, the neutral theory, the mass effect, and the patch dynamics frameworks all predict differing degrees of spatial structure resulting from dispersal and competition limitations. Here we study the relative influence of environmental gradients and spatial structure in bird assemblages of the Chilean temperate forest. We carried out bird and vegetation surveys in South American temperate forests at 147 points located in nine different protected areas in central Chile, and collected meteorological and productivity data for these localities. Species composition dissimilarities between sites were calculated, as well as three indices of bird local diversity: observed species richness, Chao estimate of richness, and Shannon diversity. A stepwise multiple regression and partial regression analyses were used to select a small number of environmental factors that predicted bird species diversity. Although diversity indices were spatially autocorrelated, environmental factors were sufficient to account for this autocorrelation. Moreover, community dissimilarities were not significantly related to distance between sites. We then tested a multivariate hypothesis about climate, vegetation, and avian diversity interactions using a structural equation modeling (SEM) approach. The SEM showed that climate and area of fragments have important indirect effects on avian diversity, mediated through changes in vegetation structure. Given the scale of this study, the metacommunity framework provides useful insights into the mechanisms driving bird assemblages in this region. Taken together, the weak spatial structure of community composition and diversity, as well as the strong environmental effects on bird diversity, support the interpretation that species sorting has a predominant role in structuring avian assemblages in the region.  相似文献   

11.
Passive acoustic monitoring could be a powerful way to assess biodiversity across large spatial and temporal scales. However, extracting meaningful information from recordings can be prohibitively time consuming. Acoustic indices (i.e., a mathematical summary of acoustic energy) offer a relatively rapid method for processing acoustic data and are increasingly used to characterize biological communities. We examined the relationship between acoustic indices and the diversity and abundance of biological sounds in recordings. We reviewed the acoustic‐index literature and found that over 60 indices have been applied to a range of objectives with varying success. We used 36 of the most indicative indices to develop a predictive model of the diversity of animal sounds in recordings. Acoustic data were collected at 43 sites in temperate terrestrial and tropical marine habitats across the continental United States. For terrestrial recordings, random‐forest models with a suite of acoustic indices as covariates predicted Shannon diversity, richness, and total number of biological sounds with high accuracy (R2 ≥ 0.94, mean squared error [MSE] ≤170.2). Among the indices assessed, roughness, acoustic activity, and acoustic richness contributed most to the predictive ability of models. Performance of index models was negatively affected by insect, weather, and anthropogenic sounds. For marine recordings, random‐forest models poorly predicted Shannon diversity, richness, and total number of biological sounds (R2 ≤ 0.40, MSE ≥ 195). Our results suggest that using a combination of relevant acoustic indices in a flexible model can accurately predict the diversity of biological sounds in temperate terrestrial acoustic recordings. Thus, acoustic approaches could be an important contribution to biodiversity monitoring in some habitats.  相似文献   

12.
Barnett A  Beisner BE 《Ecology》2007,88(7):1675-1686
While empirical studies linking biodiversity to local environmental gradients have emphasized the importance of lake trophic status (related to primary productivity), theoretical studies have implicated resource spatial heterogeneity and resource relative ratios as mechanisms behind these biodiversity patterns. To test the feasibility of these mechanisms in natural aquatic systems, the biodiversity of crustacean zooplankton communities along gradients of total phosphorus (TP) as well as the vertical heterogeneity and relative abundance of their phytoplankton resources were assessed in 18 lakes in Quebec, Canada. Zooplankton community richness was regressed against TP, the spatial distribution of phytoplankton spectral groups, and the relative biomass of spectral groups. Since species richness does not adequately capture ecological function and life history of different taxa, features which are important for mechanistic theories, relationships between zooplankton functional diversity (FD) and resource conditions were examined. Zooplankton species richness showed the previously established tendency to a unimodal relationship with TP, but functional diversity declined linearly over the same gradient. Changes in zooplankton functional diversity could be attributed to changes in both the spatial distribution and type of phytoplankton resource. In the studied lakes, spatial heterogeneity of phytoplankton groups declined with TP, even while biomass of all groups increased. Zooplankton functional diversity was positively related to increased heterogeneity in cyanobacteria spatial distribution. However, a smaller amount of variation in functional diversity was also positively related to the ratio of biomass in diatoms/chrysophytes to cyanobacteria. In all observed relationships, a greater variation of functional diversity than species richness measures was explained by measured factors, suggesting that functional measures of zooplankton communities will benefit ecological research attempting to identify mechanisms behind environmental gradients affecting diversity.  相似文献   

13.
Abstract: Conservation prioritization usually focuses on conservation of rare species or biodiversity, rather than ecological processes. This is partially due to a lack of informative indicators of ecosystem function. Biological soil crusts (BSCs) trap and retain soil and water resources in arid ecosystems and function as major carbon and nitrogen fixers; thus, they may be informative indicators of ecosystem function. We created spatial models of multiple indicators of the diversity and function of BSCs (species richness, evenness, functional diversity, functional redundancy, number of rare species, number of habitat specialists, nitrogen and carbon fixation indices, soil stabilization, and surface roughening) for the 800,000‐ha Grand Staircase‐Escalante National Monument (Utah, U.S.A.). We then combined the indicators into a single BSC function map and a single BSC biodiversity map (2 alternative types of conservation value) with an unweighted averaging procedure and a weighted procedure derived from validations performance. We also modeled potential degradation with data from a rangeland assessment survey. To determine which areas on the landscape were the highest conservation priorities, we overlaid the function‐ and diversity‐based conservation‐value layers on the potential degradation layer. Different methods for ascribing conservation‐value and conservation‐priority layers all yielded strikingly similar results (r= 0.89–0.99), which suggests that in this case biodiversity and function can be conserved simultaneously. We believe BSCs can be used as indicators of ecosystem function in concert with other indicators (such as plant‐community properties) and that such information can be used to prioritize conservation effort in drylands.  相似文献   

14.
Surrogates, such as umbrella species, are commonly used to reduce the complexity of quantifying biodiversity for conservation purposes. The presence of umbrella species is often indicative of high taxonomic diversity; however, functional diversity is now recognized as an important metric for biodiversity and thus should be considered when choosing umbrella species. We identified umbrella species associated with high taxonomic and functional biodiversity in urban areas in Switzerland. We analyzed 39,752 individuals of 574 animal species from 96 study plots and 1397 presences of 262 plant species from 58 plots. Thirty‐one biodiversity measures of 7 taxonomic groups (plants, spiders, bees, ground beetles, lady bugs, weevils and birds) were included in within‐ and across‐taxa analyses. Sixteen measures were taxonomical (species richness and species diversity), whereas 15 were functional (species traits including mobility, resource use, and reproduction). We used indicator value analysis to identify umbrella species associated with single or multiple biodiversity measures. Many umbrella species were indicators of high biodiversity within their own taxonomic group (from 33.3% in weevils to 93.8% in birds), to a lesser extent they were indicators across taxa. Principal component analysis revealed that umbrella species for multiple measures of biodiversity represented different aspects of biodiversity, especially with respect to measures of taxonomic and functional diversity. Thus, even umbrella species for multiple measures of biodiversity were complementary in the biodiversity aspects they represented. Thus, the choice of umbrella species based solely on taxonomic diversity is questionable and may not represent biodiversity comprehensively. Our results suggest that, depending on conservation priorities, managers should choose multiple and complementary umbrella species to assess the state of biodiversity. Selección de Múltiples Especies Paraguas para la Diversidad Funcional y Taxonómica para Representar la Biodiversidad Urbana  相似文献   

15.
旅游干扰下五台山不同植被景观区物种多样性特征   总被引:2,自引:0,他引:2  
利用双向指示种分析方法(Two-way indicator species analysis,TWINSPAN)和6个物种多样性指数,研究了旅游干扰下五台山不同植被景观区物种多样性的特征.结果表明:1)TWINSPAN将所有样地划分为9类植被景观区,从Ⅰ区到Ⅸ区,随着旅游干扰程度的增加,植被景观大致由乔灌草区向灌草区、草本区和居民区方向变化.2)乔木层物种的丰富度和综合多样性随着旅游干扰的减小而趋于增加,但是其均匀度没有表现出明显的规律性.3)灌木层物种的丰富度和综合多样性也随着旅游干扰的减小而趋于增加,至于其均匀度,则呈现出在中度干扰下值最大,干扰很小的地方次之,在重度干扰下则最小.4)草本层物种的丰富度、均匀度和综合多样性指数均在旅游干扰适度的地方达到了最大值,在旅游干扰很小的地方,各种值则次之,在干扰严重的地方为最小.5)从整个植被层物种多样性的角度看,随着旅游干扰程度的减少,物种丰富度指数、均匀度指数和综合多样性指数均呈现趋于增加的趋势.表4参15  相似文献   

16.
Benthic macrofauna was sampled by grab at 16 stations in Hampton Roads and the adjacent Elizabeth River, Virginia, USA. Samples were taken in February, May and August. Sampling sites and species were grouped by a classification strategy which basically consisted of the Canberra metric dissimilarity-measure and flexible and group average clustering. Following reallocations, 8 site groups and 16 species groups instructively classified the 47 sites and 93 species considered in the analysis. The sites were grouped into associations on mud, muddy-sand and sand-bottom, and those in the Elizabeth River. Species groupings distinguished a few species most frequent at Elizabeth River or mud and muddy-sand sites, larger numbers of species restricted to muddy-sand and sand or solely to sand sites, ubiquitous species, epifaunal species which were microhabitat-restricted, and seasonal species. An analysis of numerically dominant species in the different associations indicated the relative importance of ubiquitous species and seasonally abundant species. Community-structure statistics (species diversity, species richness and evenness) showed definite spatial and temporal patterns. Diversity was high at sand and muddy-sand sites and low at mud and Elizabeth River sites. This spatial pattern was predominantly one of species richness. At Elizabeth River and mud stations, diversity increased from February to August because of increased evenness, while at sand and muddy-sand stations, diversity peaked in May in response to both high species richness and high evenness. The applicability of community concepts, the causes of substrate specificity, seasonality and species diversity, and the effects of pollution on community structure are discussed.Contribution No. 553, Virginia Institute of Marine Science, Gloucester Point, Virginia, USA.  相似文献   

17.
曹云生  杨新兵  张伟  宋庆丰  张建华 《生态环境》2010,19(12):2840-2844
通过野外调查取样,应用Menhinick丰富度指数、Simpson指数、Shannon-Wiener指数和Pielou均匀度指数研究了冀北山区12种典型森林群落内的草本植物多样性规律,并采用典范对应分析(CCA)方法研究其分布与地形的关系。结果表明:不同的群落类型草本植物的组成和多样性指数不同,山杨(Populus davidiana)纯林的种数最多为34种,黑桦(Betula dahurica Pall)纯林的种数最少为19种,其Simpson指数、Shannon-Wiener指数最高,分别为0.927 3和2.879 6;在1 200~1 700 m之间,随海拔升高物种多样性指数、均匀度指数和丰富度指数呈正相关性,但没有线性上升的趋势关系;选取的地形因子对样点草本的影响程度大小为:坡向〉海拔〉坡度〉坡位〉坡形,坡向是样点草本植物空间差异的最主要地形制约因子,环境解释率为98.7%,证明排序可信。  相似文献   

18.
Abstract:  We assessed the conservation priority of 18 freshwater ecoregions in southern South America on the basis of Aegla (genus of freshwater crabs) genetic diversity and distribution. Geographical distributions for 66 Aegla species were taken from the literature and plotted against ecoregions and main river basins of southern South America. Species richness and number of threatened and endemic species were calculated for each area. To assess taxonomic and phylogenetic diversity, we generated a molecular phylogeny based on DNA sequences for one nuclear (28S) and 4 mitochondrial (12S, 16S, COI, and COII) genes. All species richness and phylogenetic methods agreed, to a large extent, in their rankings of the importance of conservation areas, as indicated by the Spearman's rank correlation coefficient ( p < 0.01); nonetheless, some of the lowest correlations were observed between taxonomic and phylogenetic diversity indices. The 5 ecoregions of the Laguna dos Patos Basin (Eastern Brazil), Central Chile, South Brazilian Coast, Chilean Lakes, and Subtropical Potamic Axis (northern Argentina and southern Uruguay and Paraguay) had the highest biodiversity scores. Conservation of these regions will preserve the largest number of species and the greatest amount of genetic diversity within the South American freshwater Aegla fauna. Biodiversity across rivers and within areas was heterogeneously distributed in the ecoregions of Upper Paraná, Ribeira do Iguape, Upper Uruguay, and South Brazilian Coast (i.e., one river showed significantly more biodiversity than any other river from the same ecoregion), but homogeneously distributed in the other ecoregions. Hence, conservation plans in the former regions will potentially require less effort than plans in the latter regions.  相似文献   

19.
Understanding threatened species diversity is important for long‐term conservation planning. Geodiversity—the diversity of Earth surface materials, forms, and processes—may be a useful biodiversity surrogate for conservation and have conservation value itself. Geodiversity and species richness relationships have been demonstrated; establishing whether geodiversity relates to threatened species’ diversity and distribution pattern is a logical next step for conservation. We used 4 geodiversity variables (rock‐type and soil‐type richness, geomorphological diversity, and hydrological feature diversity) and 4 climatic and topographic variables to model threatened species diversity across 31 of Finland's national parks. We also analyzed rarity‐weighted richness (a measure of site complementarity) of threatened vascular plants, fungi, bryophytes, and all species combined. Our 1‐km2 resolution data set included 271 threatened species from 16 major taxa. We modeled threatened species richness (raw and rarity weighted) with boosted regression trees. Climatic variables, especially the annual temperature sum above 5 °C, dominated our models, which is consistent with the critical role of temperature in this boreal environment. Geodiversity added significant explanatory power. High geodiversity values were consistently associated with high threatened species richness across taxa. The combined effect of geodiversity variables was even more pronounced in the rarity‐weighted richness analyses (except for fungi) than in those for species richness. Geodiversity measures correlated most strongly with species richness (raw and rarity weighted) of threatened vascular plants and bryophytes and were weakest for molluscs, lichens, and mammals. Although simple measures of topography improve biodiversity modeling, our results suggest that geodiversity data relating to geology, landforms, and hydrology are also worth including. This reinforces recent arguments that conserving nature's stage is an important principle in conservation.  相似文献   

20.
Abstract: Identification of priority areas is a fundamental goal in conservation biology. Because of a lack of detailed information about species distributions, conservation targets in the Zhoushan Archipelago (China) were established on the basis of a species–area–habitat relationship (choros model) combined with an environmental cluster analysis (ECA). An environmental‐distinctness index was introduced to rank areas in the dendrogram obtained with the ECA. To reduce the effects of spatial autocorrelation, the ECA was performed considering spatial constraints. To test the validity of the proposed index, a principal component analysis–based environmental diversity approach was also performed. The priority set of islands obtained from the spatially constrained cluster analysis coupled with the environmental‐distinctness index had high congruence with that from the traditional environmental‐diversity approach. Nevertheless, the environmental‐distinctness index offered the advantage of giving hotspot rankings that could be readily integrated with those obtained from the choros model. Although the Wilcoxon matched‐pairs test showed no significant difference among the rankings from constrained and unconstrained clustering process, as indicated by cophenetic correlation, spatially constrained cluster analysis performed better than the unconstrained cluster analysis, which suggests the importance of incorporating spatial autocorrelation into ECA. Overall, the integration of the choros model and the ECA showed that the islands Liuheng, Mayi, Zhoushan, Fodu, and Huaniao may be good candidates on which to focus future efforts to conserve regional biodiversity. The 4 types of priority areas, generated from the combination of the 2 approaches, were explained in descending order on the basis of their conservation importance: hotspots with distinct environmental conditions, hotspots with general environmental conditions, areas that are not hotspots with distinct environmental conditions, and areas that are not hotspots with general environmental conditions.  相似文献   

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