Assessing patterns of plant endemism in neotropical uplands

Conservation of biodiversity will necessitate choices among areas, taxa, and land-use patterns. Lack of data on distribution and pattern in biodiversity makes these difficult decisions even more problematic for those charged with the conservation and sustainable use of the diversity of life. Quantitative methods have promise in helping with this task in that they allow people to make their values explicit, and they also allow representation and comparison of many different types of data. In this article I examine patterns of species richness and range-size rarity, or endemism, in the Neotropics with a data set from the genusSolanum (Solanaceae). Distribution data for 180 species of forest-dwelling solanums were analyzed. Patterns of species richness, range-size rarity (endemism), and several area-selection methods were examined. Montane areas are relatively rich both in all species and in endemic species, with maximal peaks in the Andes. The peak of species richness coincides with the domain (i.e., continental) midpoint (9°30′ S latitude), suggesting that the pattern observed may be partly due to the geometry of species ranges. TheSolanum results are compared with those obtained for other taxonomic groups in the Neotropics, and problems with quantitative data sets in conservation are discussed. Collecting deficit, parochial taxonomy, and habitat destruction, both historical and current, are all factors that will affect the utility of such analyses. It is clear that if conservation is to work on the ground, we need to know more about what occurs in the montane Neotropics and that continued work at a basic taxonomic level is essential to our ultimate ability to conserve biological diversity.     

Species richness and endemism of plant and bird communities along two gradients of elevation, humidity and land use in the Bolivian Andes

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.     

Response of plant species and life form diversity to variable fire histories and biomass in the jarrah forest of south‐west Australia

Frequent fires reduce the abundance of woody plant species and favour herbaceous species. Plant species richness also tends to increase with decreasing vegetation biomass and cover due to reduced competition for light. We assessed the influence of variable fire histories and site biomass on the following diversity measures: woody and herbaceous species richness, overall species richness and evenness, and life form evenness (i.e. the relative abundance or dominance among six herbaceous and six woody plant life forms), across 16 mixed jarrah (Eucalyptus marginata) and marri (Corymbia calophylla) forest stands in south‐west Australia. Fire frequency was defined as the total number of fires over a 30‐year period. Overall species richness and species evenness did not vary with fire frequency or biomass. However, there were more herbaceous species (particularly rushes, geophytes and herbs) where there were fewer shrubs and low biomass, suggesting that more herbaceous species coexist where dominance by shrubs is low. Frequently burnt plots also had lower number and abundance of shrub species. Life form evenness was also higher at both high fire frequency and low biomass sites. These results suggest that the impact of fire frequency and biomass on vegetation composition is mediated by local interactions among different life forms rather than among individual species. Our results demonstrate that measuring the variation in the relative diversity of different woody and herbaceous life forms is crucial to understanding the compositional response of forests and other structurally complex vegetation communities to changes in disturbance regime such as increased fire frequency.     

Stochastic losses of fire‐dependent endemic herbs revealed by a 65‐year chronosequence of dispersal‐limited woody plant encroachment

The factors responsible for maintaining diverse groundcover plant communities of high conservation value in frequently burned wet pine savannas are poorly understood. While most management involves manipulating extrinsic factors important in maintaining species diversity (e.g., fire regimes), most ecological theory (e.g., niche theory and neutral theory) examines how traits exhibited by the species promote species coexistence. Furthermore, although many ecologists focus on processes that maintain local species diversity, conservation biologists have argued that other indices (e.g., phylogenetic diversity) are better for evaluating assemblages in terms of their conservation value. I used a null model that employed beta‐diversity calculations based on Raup–Crick distances to test for deterministic herbaceous species losses associated with a 65‐year chronosequence of woody species encroachment within each of three localities. I quantified conservation value of assemblages by measuring taxonomic distinctness, endemism, and floristic quality of plots with and without woody encroachment. Reductions in herb species richness per plot attributable to woody encroachment were largely stochastic, as indicated by a lack of change in the mean or variance in beta‐diversity caused by woody encroachment in the savannas studied here. Taxonomic distinctness, endemism, and floristic quality (when summed across all species) were all greater in areas that had not experienced woody encroachment. However, when corrected for local species richness, only average endemism and floristic quality of assemblages inclusive of herbs and woody plants were greater in areas that had not experienced woody encroachment, due to the more restricted ranges and habitat requirements of herbs. Results suggest that frequent fires maintain diverse assemblages of fire‐dependent herb species endemic to the region. The stochastic loss of plant species, irrespective of their taxonomic distinctness, to woody encroachment suggests that the relevance of niche partitioning or phylogenetic diversity to the management of biodiversity in wet pine savannas is minimal.     

Features and distribution patterns of Chinese endemic seed plant species

We compiled and identified a list of Chinese. endemic seed plant species based on a large number of published References and expert reviews. The characters of these seed plant species and their distribution patterns were described at length. China is rich in endemic seed plants, with a total of 14 939 species (accounting for 52.1%of its total seed plant species) belonging to 1584 genera and 191 families. Temperate families and genera have a significantly higher proportion of endemism than cosmopolitan and tropical ones. The most primitive and derived groups have significantly higher endemism than the other groups. The endemism of tree, shrub, and liana or vine is higher than that of total species; in contrast, the endemism of herb is lower than that of total species. Geographically,these Chinese endemic plants are mainly distributed in Yunnan and Sichuan provinces, southwest China. Species richness and proportion of these endemic plants decrease with increased latitude and have a unimodal response to altitude. The peak value of proportion of endemism is at higher altitudes than that of total species and endemic species richness. The proportions of endemic shrub, liana or vine, and herb increase with altitude and have a clear unimodal curve. In contrast, the proportion of tree increases with altitude, with a sudden increase at～4000 m and has a completely different model. To date, our study provides the most comprehensive list of Chinese endemic seed plant species and their basic composition and distribution features.     

Floristic diversity of an eastern Mediterranean dwarf shrubland: the importance of soil pH

Questions: Does plant species richness and composition of eastern Mediterranean dwarf shrubland (phrygana) correlate with soil pH? How important is the effect of pH on species diversity in relation to other environmental factors in this ecosystem? What is the evolutionary background of the diversity–pH relationship? Location: Western Crete, Greece. Methods: Species composition of vascular plants, soil and other environmental variables were sampled in 100‐m² plots on acidic and basic bedrock in phrygana vegetation. The relationships between species composition and environmental variables (including climate) were tested using canonical correspondence analysis, and relationships between species richness and environment using correlation and regression analyses. Data were analysed separately for different plant functional types based on life form and life span. Results: Although soil pH varied across a narrow range (5.9‐8.1), species composition changed significantly along the pH gradient within all plant functional types. For most functional types, the effect of soil pH on species composition was stronger than that of other environmental variables. Species richness of annuals, geophytes and suffruticose chamaephytes increased with soil pH, while richness of hemicryptophytes and shrubs was not correlated with pH. Conclusions: The results are consistent with the evolutionary species pool hypothesis. High numbers of calcicole annuals, geophytes and suffruticose chamaephytes may be a result of the evolution of these groups on base‐rich dry soils in the Mediterranean climate. In contrast, hemicryptophytes, a life form typical of the temperate zone, evolved on both acidic and basic soils and therefore their species numbers do not respond to soil pH across the narrow range studied. The lack of a relationship between shrub species richness and pH is difficult to explain: it may reflect the more diverse or older origin of Mediterranean woody species and their conservative niches.     

Geographic patterns in the distribution of Palearctic songbirds

A database was created of digitized equal area distribution maps of 3,036 phylogenetic species of Palearctic songbirds. Biogeographic patterns are reported for two data sets: (1) including all passeriform bird species reported as breeding within the boundaries of our study map, (2) passeriform species restricted in their distribution to our study region, thus excluding the partly extra-limital taxa. With respect to the data set excluding partly extra-limital taxa, the average range size is 238 grid cells (grid cell area: 4,062 km²). Analysis of the geographic distribution of species richness for the full data set showed several hotspot regions, mostly located in mountainous areas. The index of range-size rarity identified similar hotspot regions as that for species richness, albeit that the range-size rarity de-emphasized the central Siberian hotspot. Range-size rarity hotspots that are not evident on the measure of species richness concern a great number of islands. Much more prominent on the index of range-size rarity are the Atlas Mountains of northern Africa, the Jabal al Akhdar region in NE Libya, and the eastern border of the Mediterranean. Restricting the analysis of geographic variation to the 25% of the species with smallest ranges resulted in a greatly simplified pattern of hotspots. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

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.     

Patterns and correlates of plant diversity differ between common and rare species in a neotropical dry forest

Determining which factors affect species richness is important for conservation theory and practice. However, richness of common and rare species may be affected by different factors. We use an extensive inventory of woody plants from a tropical dry forest landscape in Yucatan, Mexico to assess the unique effects of environmental variables, spatial dependence of sampling sites, forest stand age and the combined effect of all groups of variables on species richness of woody plants with different levels of rarity (common, intermediate, rare, very rare)—according to their abundance, habitat specificity and spatial distribution range in the landscape. Analyzing separately common species and those with different levels of rarity uncovered contrasting patterns and correlates of species richness that were not apparent when focusing on all woody plants. In particular, richness of common and intermediate species was influenced mainly by environmental factors, whereas richness of very rare species was affected mostly by the unique effect of spatial dependence of sampling sites, suggesting a main role of environmental filtering and dispersal limitation, respectively. However, common and very rare species also responded inversely to some landscape metrics, revealing contrasting environmental preferences of these groups of species. These contrasting results suggest different underlying mechanisms and the need for very different conservation strategies. Therefore, basic and applied research on tropical forest biodiversity should consider separately species with different levels of rarity, focusing on which factors control variation in each level, and paying special attention to very rare species, generally the most specious and vulnerable to local extinction.     

Can distribution models help refine inventory‐based estimates of conservation priority? A case study in the Eastern Arc forests of Tanzania and Kenya

Aim Data shortages mean that conservation priorities can be highly sensitive to historical patterns of exploration. Here, we investigate the potential of regionally focussed species distribution models to elucidate fine‐scale patterns of richness, rarity and endemism. Location Eastern Arc Mountains, Tanzania and Kenya. Methods Generalized additive models and land cover data are used to estimate the distributions of 452 forest plant taxa (trees, lianas, shrubs and herbs). Presence records from a newly compiled database are regressed against environmental variables in a stepwise multimodel. Estimates of occurrence in forest patches are collated across target groups and analysed alongside inventory‐based estimates of conservation priority. Results Predicted richness is higher than observed richness, with the biggest disparities in regions that have had the least research. North Pare and Nguu in particular are predicted to be more important than the inventory data suggest. Environmental conditions in parts of Nguru could support as many range‐restricted and endemic taxa as Uluguru, although realized niches are subject to unknown colonization histories. Concentrations of rare plants are especially high in the Usambaras, a pattern mediated in models by moisture indices, whilst overall richness is better explained by temperature gradients. Tree data dominate the botanical inventory; we find that priorities based on other growth forms might favour the mountains in a different order. Main conclusions Distribution models can provide conservation planning with high‐resolution estimates of richness in well‐researched areas, and predictive estimates of conservation importance elsewhere. Spatial and taxonomic biases in the data are essential considerations, as is the spatial scale used for models. We caution that predictive estimates are most uncertain for the species of highest conservation concern, and advocate using models and targeted field assessments iteratively to refine our understanding of which areas should be prioritised for conservation.     

Species richness in plant genera disjunct between temperate eastern Asia and North America

The species richness of 109 amphi-Pacific disjunct genera was examined in eastern Asia and North America. Although the entire flora of eastern Asia contains approximately one-third more species than that of North America, the difference in species richness among disjunct taxa is less. When woody and herbaceous genera are considered separately, the former exhibit a strong diversity bias favouring eastern Asia whereas there is no significant difference in diversity between continents among herbaceous genera. This result is not due to habitat differences between woody and herbaceous genera, because the disjunct herbs inhabit primarily moist forests and woodlands. This result is also not related to relative phylogenetic advancement, even though older major lineages of plants tend to have a predominance of woody taxa. Woody genera are distributed in lower latitudes than herbaceous genera on both continents, and both woody and herbaceous genera are distributed in lower latitudes in eastern Asia than in North America. The North American temperate flora is primarily a relict of a flora form 7 more widespread throughout the Northern Hemisphere. Contemporary patterns of diversity suggest that the effects of climate changes in the late Tertiary were less severe in eastern Asia and promoted diversification, but were more severe in North America and may have caused widespread extinction. The difference in the effect of climate change on diversity in herbaceous and woody lineages reflects the different ecological relationships of species having these contrasting life forms. Clearly, the contemporary floras of eastern Asia and North America bear the imprint of history and emphasize the important interface between ecological relationships and evolutionary responses.     

Latitudinal patterns of range size and species richness of New World woody plants

Aim  Relationships between range size and species richness are contentious, yet they are key to testing the various hypotheses that attempt to explain latitudinal diversity gradients. Our goal is to utilize the largest data set yet compiled for New World woody plant biogeography to describe and assess these relationships between species richness and range size.
Location  North and South America.
Methods  We estimated the latitudinal extent of 12,980 species of woody plants (trees, shrubs, lianas). From these estimates we quantified latitudinal patterns of species richness and range size. We compared our observations with expectations derived from two null models.
Results   Peak richness and the smallest- and largest-ranged species are generally found close to the equator. In contrast to prominent diversity hypotheses: (1) mean latitudinal extent of tropical species is greater than expected; (2) latitudinal extent appears to be decoupled from species richness across New World latitudes, with abrupt transitions across subtropical latitudes; and (3) mean latitudinal extents show equatorial and north temperate peaks and subtropical minima. Our results suggest that patterns of range size and richness appear to be influenced by three broadly overlapping biotic domains (biotic provinces) for New World woody plants.
Main conclusions  Hypotheses that assume a direct relationship between range size and species richness may explain richness patterns within these domains, but cannot explain gradients in richness across the New World.     

The implications of different species concepts for describing biodiversity patterns and assessing conservation needs for African birds

It has been suggested that switching from the widely used Biological Species Concept to a Phylogenetic Species Concept, would result in the appearance of hitherto neglected patterns of endemism. The problem has mainly been analyzed with respect to endemic taxa and for rather limited geographical regions, but will here be analysed for the entire resident avifauna of sub-Saharan Africa. A database of African bird distributions was re-edited to create two new datasets representing 1572 biological species and 2098 phylogenetic species. Species richness patterns were virtually identical with the two taxonomies, and only subtle changes were found in the geographical variation in range-size rarity sum. However, there were some differences in the most range-restricted species, with increased complexity of long-recognized centres of endemism. Overall, then, the large-scale biogeographic patterns are robust to changes in species concepts. This reflects the aggregated nature of endemism, with certain areas acting as "species pumps" and large intervening areas being characterised by a predominance of widespread species which distribute themselves in accordance with contemporary environmental conditions. The percentages of phylogenetic and threatened species captured in a BSC near-minimum set of 64 grid-cells and a PSC near-maximum set, with the same number of grid-cells, are very similar.     

Variation in plant species richness of different life forms along a subtropical elevation gradient in the Himalayas, east Nepal

Aim To explore the variation in species richness along a subtropical elevation gradient, and evaluate how climatic variables explain the richness of the different life forms such as trees, shrubs, climbers, herbs and ferns. Location The study was made in a subtropical to warm temperate region in the south‐eastern part of Nepal, between 100 and 1500 m above sea level (a.s.l.). Methods The number of species was counted in six plots (50 × 20 m) in each of the 15 100 m elevation bands covering the main physiognomic structures along an imaginary transect. Each species recorded was assigned to a life form. Potential evapotranspiration (PET, i.e. energy), mean annual rainfall (MAR), and their ratio (MI = moisture index) were evaluated as explanatory variables by means of generalized linear models (GLM). Each variable was tested individually, and in addition MAR and PET were used to test the water‐energy dynamics model for each life form. Results The richness of herbaceous species, including herbaceous climbers, was unrelated to any of the climate variables. PET was strongly negatively correlated with elevation, and the following relationships were found between increasing PET and richness: (i) shrubs, trees and total species (sum of all life forms) showed unimodal responses (ii) ferns decreased monotonically, and (iii) woody climbers increased monotonically. Richness of all woody groups increased monotonically with MAR and MI. The water‐energy dynamics model explained 63% of the variation in shrubs, 67% for trees and 70% for woody species combined. Main conclusions For the various herbaceous life forms (forbs, grasses, and herbaceous climbers) we found no significant statistical trends, whereas for woody life forms (trees, shrubs, and woody climbers) significant relationships were found with climate. E.M. O’Brien's macro‐scale model based on water‐energy dynamics was found to explain woody species richness at a finer scale along this elevational‐climatic gradient.     

Plant diversity patterns in the Aljibe Mountains (S. Spain): a comprehensive account

The Aljibe Mountains are located in the southern tip of the Iberian Peninsula and have a remarkable biogeographical interest. The complete plant species list (trees, climbers, shrubs, perennial and annual herbs, ferns, lichens, bryophytes and macroscopic algae) was recorded in four 0.1 ha plots from each of the most representative community types (Quercus suber woodland, Q. canariensis forest, open heathland and Q. coccifera shrubland). Up to 119 plant species were found in total in the Q. suber woodland plot. The diversity of woody plants was analysed from 44 samples of cover (100 m line), and the herbaceous layer was explored in 200 quadrats (of 0.5 × 0.5 m). Three biodiversity components (species richness, endemism, and taxonomic singularity) were evaluated in both shrub and herbaceous layers. Open heathlands showed the highest richness of endemic species, both woody and herbaceous. The highest number of woody species was found in the evergreen Q. suber woodland, and of herbaceous species in the semi-deciduous Q. canariensis woodland. Taxonomic singularity was higher in Q. canariensis woodlands and Q. coccifera shrublands for woody species, but there were no significant differences in the herbaceous layer. Local species diversity of heathlands in this region resembles that of South African heathlands (fynbos), despite the obvious geographic and floristic distance, and contrasts with the low diversity of biogeographically closer, European temperate heathlands. The Aljibe Mountains show high diversity values for different life forms (from trees to mosses) and spatial scales (from community to region), and are rich in endemic species. Thus, this area should be recognised as a relevant unit within the Mediterranean plant diversity hot spots.     

浙江仙居俞坑森林群落物种多样性研究

分别采用物种丰富度、物种多样性指数和群落均匀度指标对浙江省仙居县俞坑森林群落的物种多样性进行测定和分析。结果表明：本木植物的物种多样性以生境优越的常绿阔叶林为高,木本植物的物种丰富度、物种多样性指数明显大于草本植物。在群落垂直结构中,木本植物等2层的物种丰富度、物种多样性指数均显著大于第1层。物种丰富度以木本第3层最大,草本层最小;而物种多样性指数、群落均匀度则以木本第2层最大、草本层最小。木本植物各层次、草本层的物种多样性各项指标在群落各样地间均有一定的差异。     

Impact of two wildfires on endemic granite outcrop vegetation in Western Australia

Abstract. In seasonally dry regions of the world fire is a recurring disturbance but little is known of how fire interacts with granite outcrop vegetation. We hypothesize that the floristic composition in granite vegetation, usually attributed to the edaphic environment, may also reflect the impact of disturbances such as fire. Dramatic differences in floristic composition and cover over 13 years and two fires were observed in vegetation on a Western Australian granite outcrop. This was very marked in the first year following the two fires, with annuals and geophytes showing the greatest turnover of species. Even among the perennial shrubs there was considerable turnover in a number of obligate seeders. After the first fire the number of species declined for woody perennials, herbaceous perennials and annuals, remained unchanged for perennial grasses and sedges, and varied with highest richness 4 yr after fire for geophytes. Demographic studies of two endemic woody obligate seeders and three endemic mallee eucalypt resprouters similarly showed dramatic differences within and between species in seedling recruitment following the two fires. Fire does have a significant impact on the floristic composition of semi‐arid granite outcrop vegetation communities. Studies on other granite outcrop systems are needed to test the generality of this conclusion.     

Grazing in remnant woodland vegetation: changes in species composition and life form groups

Abstract. Grazing by domestic livestock in native woodlands can have major effects on ecosystem functioning by the removal of plant species that form important functional groups. This paper documents the changes in floristics in a large group of remnants of native woodland left after agricultural clearing in southwestern Australia. Species richness and diversity were significantly reduced in remnants and the proportion of exotic species increased. Detrended Correspondence Analysis (DCA) was used to identify floristic and environmental patterns among plots and identified two distinct groups based on grazing intensity. This indicated that the significance of the relationship between grazing effects and DCA floristic axes was greater than edaphic characteristics that normally influence floristic patterns. Floristic characteristics of sites that were influencing the position of plots on the ordination diagram included proportion of exotic species and proportion of native perennial shrubs and herbs. Numbers of species of native shrubs and perennial herbs were significantly reduced in grazed plots and numbers of exotic annual grasses and herbs were significantly higher. Other life form groups such as native perennial grasses and geophytes were not significantly affected by grazing. Reproductive strategies of perennial species showed a significant decrease in numbers of resprouters and a significant increase in numbers of facultative seeder/sprouters. Exclosure plots showed increases in number and cover of perennial shrubs and herbs after three years whereas number and cover of exotic species did not change. Time series DCA showed that the floristic composition of exclosure plots in grazed sites became closer to that of the ungrazed sites.     

青藏高原植物群落样方数据集

为便于了解青藏高原植被特殊物种组成、群落特征及分布格局, 该文利用2018-2021年在青藏高原不同区域内调查的338个样地、共758个样方的数据, 分析了高原植物群落的物种组成、区系特征和植被分类, 整合形成青藏高原植物群落样方数据集。结果表明: 青藏高原高寒和温性植物群落758个样方中, 共有植物65科279属837种; 其中, 物种数最多的5个科依次是菊科(134种)、禾本科(88种)、豆科(75种)、蔷薇科(43种)和莎草科(40种), 物种数最多的5个属依次是蒿属(Artemisia, 29种)、马先蒿属(Pedicularis, 27种)、风毛菊属(Saussurea, 25种)、黄耆属(Astragalus, 23种)和早熟禾属(Poa, 23种)。植物区系主要由温带(145属)和世界广布(36属)的成分所组成。物种的生长型以草本(83.51%)和灌木(10.87%)为主, 草本和木本的生活型分别以多年生草本(88.23%)和落叶灌木(83.67%)为主。338个样地可以划分为4个植被型组, 10个植被型, 20个植被亚型, 78个群系组和117个群系, 其中草原群系34个, 草甸群系33个, 荒漠群系33个, 灌丛群系14个和针叶林群系3个。该数据集覆盖青藏高原绝大部分高寒灌丛、高寒草原、高寒草甸、高寒荒漠、温性草原和温性荒漠植被区域, 可为研究高原植被特征和地带性分异规律, 气候变化和人类活动对高原植被的影响及其生态恢复提供坚实的数据基础, 同时为下一代中国植被图的更新提供参考。     

Global diversity of land planarians (Platyhelminthes, Tricladida, Terricola): a new indicator-taxon in biodiversity and conservation studies

Biodiversity conservation requires prioritization of areas for in situ conservation. In that perspective, the present study documents the global diversity of a component of the soil macrofauna, the land planarians, and concerns an exploratory analysis of their possible role as indicators of biodiversity. Diversity is described by three quantitative methods: (1) hotspots of species richness, selecting areas richest in species, (2) hotspots of range-size rarity, identifying areas richest in narrowly endemic species, and (3) complementarity, prioritizing areas according to their greatest combined species richness. The biodiversity measures of species richness and range-size rarity show a great correspondence in the identification of hotspots of diversity; both measures identify the following seven areas as the most biodiverse for land planarians: Sao Paulo, Florianopolis, western Java, Tasmania, Sri Lanka, North Island/New Zealand, and Sydney. It is discussed to what extent the results for the land planarians correspond with those obtained in other studies that assessed biodiversity hotspots for taxa on a global scale. It is noteworthy that land planarians identify a few global hotspots of diversity that generally do not feature, or only have low rankings, in other studies: New Zealand, southeastern Australia, and Tasmania.