首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 15 毫秒
1.

Aim

Land use is a main driver of biodiversity loss worldwide. However, quantifying its effects on global plant diversity remains a challenge due to the limited availability of data on the distributions of vascular plant species and their responses to land use. Here, we estimated the global extinction threat of land use to vascular plant species based on a novel integration of an ecoregion-level species-area model and the relative endemism richness of the ecoregions.

Location

Global.

Methods

First, we assessed ecoregion-level extinction threats using a countryside species–area relationship model based on responses of local plant richness to land use types and intensities and a high-resolution global land use map. Next, we estimated global species extinction threat by multiplying the relative endemism richness of each ecoregion with the ecoregion-level extinction threats.

Results

Our results indicate that 11% of vascular plant species are threatened with global extinction. We found the largest extinction threats in the Neotropic and Palearctic realms, mainly due to cropland of minimal and high intensity, respectively.

Main Conclusions

Our novel integration of the countryside species–area relationship and the relative endemism richness allows for the identification of hotspots of global extinction threat, as well as the contribution of specific land use types and intensities to this threat. Our findings inform where the development of measures to protect or restore plant diversity globally are most needed.  相似文献   

2.
Vamosi JC  Wilson JR 《Ecology letters》2008,11(10):1047-1053
The phylogenetic clustering of extinction may jeopardize the existence of entire families and genera, which can result in elevated reductions of evolutionary history (EH), trait diversity, and ecosystem functioning. Analyses of globally threatened birds and mammals suggest current extinction threats will result in a much higher loss of EH than random extinction scenarios, while the analyses of the taxonomical distribution of regionally rare plants find the opposite pattern. The disproportionately high number of rare plant species within species-rich families potentially suggests that lower losses of plant EH will be sustained than expected under random extinction. We show that at a global scale, this is not the case. Species-poor (especially monotypic) angiosperm families are more often at risk of extinction than expected. Because these high-risk species-poor families are as evolutionarily distinct as other families, the expected family-level EH plausibly lost in the next 100 years exceeds that predicted from random extinction by up to approximately 1165 million years.  相似文献   

3.
The Earth's evolutionary history is threatened by species loss in the current sixth mass extinction event in Earth's history. Such extinction events not only eliminate species but also their unique evolutionary histories. Here we review the expected loss of Earth's evolutionary history quantified by phylogenetic diversity (PD) and evolutionary distinctiveness (ED) at risk. Due to the general paucity of data, global evolutionary history losses have been predicted for only a few groups, such as mammals, birds, amphibians, plants, corals and fishes. Among these groups, there is now empirical support that extinction threats are clustered on the phylogeny; however this is not always a sufficient condition to cause higher loss of phylogenetic diversity in comparison to a scenario of random extinctions. Extinctions of the most evolutionarily distinct species and the shape of phylogenetic trees are additional factors that can elevate losses of evolutionary history. Consequently, impacts of species extinctions differ among groups and regions, and even if global losses are low within large groups, losses can be high among subgroups or within some regions. Further, we show that PD and ED are poorly protected by current conservation practices. While evolutionary history can be indirectly protected by current conservation schemes, optimizing its preservation requires integrating phylogenetic indices with those that capture rarity and extinction risk. Measures based on PD and ED could bring solutions to conservation issues, however they are still rarely used in practice, probably because the reasons to protect evolutionary history are not clear for practitioners or due to a lack of data. However, important advances have been made in the availability of phylogenetic trees and methods for their construction, as well as assessments of extinction risk. Some challenges remain, and looking forward, research should prioritize the assessment of expected PD and ED loss for more taxonomic groups and test the assumption that preserving ED and PD also protects rare species and ecosystem services. Such research will be useful to inform and guide the conservation of Earth's biodiversity and the services it provides.  相似文献   

4.
There is an increasing interest in measuring loss of phylogenetic diversity and evolutionary distinctiveness which together depict the evolutionary history of conservation interest. Those losses are assessed through the evolutionary relationships between species and species threat status or extinction probabilities. Yet, available information is not always sufficient to quantify the threat status of species that are then classified as data deficient. Data‐deficient species are a crucial issue as they cause incomplete assessments of the loss of phylogenetic diversity and evolutionary distinctiveness. We aimed to explore the potential bias caused by data‐deficient species in estimating four widely used indices: HEDGE, EDGE, PDloss, and Expected PDloss. Second, we tested four different widely applicable and multitaxa imputation methods and their potential to minimize the bias for those four indices. Two methods are based on a best‐ vs. worst‐case extinction scenarios, one is based on the frequency distribution of threat status within a taxonomic group and one is based on correlates of extinction risks. We showed that data‐deficient species led to important bias in predictions of evolutionary history loss (especially high underestimation when they were removed). This issue was particularly important when data‐deficient species tended to be clustered in the tree of life. The imputation method based on correlates of extinction risks, especially geographic range size, had the best performance and enabled us to improve risk assessments. Solving threat status of DD species can fundamentally change our understanding of loss of phylogenetic diversity. We found that this loss could be substantially higher than previously found in amphibians, squamate reptiles, and carnivores. We also identified species that are of high priority for the conservation of evolutionary distinctiveness.  相似文献   

5.
羊肚菌的多样性、演化历史及栽培研究进展   总被引:11,自引:0,他引:11  
杜习慧  赵琪  杨祝良 《菌物学报》2014,33(2):183-197
羊肚菌属Morchella真菌是一类珍稀食用和药用真菌,具有重要的经济和科研价值。从羊肚菌属的分类研究、物种多样性、物种分布与生态多样性、演化历史、人工栽培等方面,对新近的研究成果进行了综述,总结了世界羊肚菌研究中取得的主要成绩,指出了仍然存在的主要问题及解决这些问题的相应思路和对策。  相似文献   

6.
Nations have committed to ambitious conservation targets in response to accelerating rates of global biodiversity loss. Anticipating future impacts is essential to inform policy decisions for achieving these targets, but predictions need to be of sufficiently high spatial resolution to forecast the local effects of global change. As part of the intercomparison of biodiversity and ecosystem services models of the Intergovernmental Science‐Policy Platform on Biodiversity and Ecosystem Services, we present a fine‐resolution assessment of trends in the persistence of global plant biodiversity. We coupled generalized dissimilarity models, fitted to >52 million records of >254 thousand plant species, with the species–area relationship, to estimate the effect of land‐use and climate change on global biodiversity persistence. We estimated that the number of plant species committed to extinction over the long term has increased by 60% globally between 1900 and 2015 (from ~10,000 to ~16,000). This number is projected to decrease slightly by 2050 under the most optimistic scenario of land‐use change and to substantially increase (to ~18,000) under the most pessimistic scenario. This means that, in the absence of climate change, scenarios of sustainable socio‐economic development can potentially bring extinction risk back to pre‐2000 levels. Alarmingly, under all scenarios, the additional impact from climate change might largely surpass that of land‐use change. In this case, the estimated number of species committed to extinction increases by 3.7–4.5 times compared to land‐use‐only projections. African regions (especially central and southern) are expected to suffer some of the highest impacts into the future, while biodiversity decline in Southeast Asia (which has previously been among the highest globally) is projected to slow down. Our results suggest that environmentally sustainable land‐use planning alone might not be sufficient to prevent potentially dramatic biodiversity loss, unless a stabilization of climate to pre‐industrial times is observed.  相似文献   

7.
为评估西双版纳国家级自然保护区对樟科这一重要植物类群进化潜力的保护情况, 揭示将物种进化历史纳入生物多样性保护评估的重要性, 本研究通过对西双版纳地区长期的野外调查并查阅标本记录与文献资料, 整理出该地区樟科13属121种物种的具体分布信息, 以植物条形码ITS序列作为分子标记构建了反映整个西双版纳地区樟科植物系统发育关系的系统发育树。我们以此为基础, 从物种层面分析了各物种的进化特异性(evolutionary distinctiveness, ED), 从区域层面分析了自然保护区内、外以及32个行政乡镇的系统发育多样性(phylogenetic diversity, PD), 并结合物种丰富度(species richness, SR)与物种濒危等级, 综合探讨了西双版纳国家级自然保护区对樟科植物进化历史的保护情况。研究发现, 西双版纳国家级自然保护区仅拥有整个西双版纳地区54.5%的樟科物种数, 却保护了该地区樟科植物约88.8%的进化历史, 没有被列入保护范围但却拥有高系统发育多样性的区域有打洛镇、易武乡等。就物种而言, 进化特异性相对较高的19个物种中, 有5种(26.3%)在自然保护区内没有分布; 濒危等级高的54个物种中, 有20种(37.0%)在自然保护区没有分布, 同时拥有高进化特异性和濒危等级的物种仅有1种不在保护区内分布。结果表明, 虽然西双版纳国家级自然保护区对樟科这一植物类群的系统发育多样性以及高保护价值物种的保护较好, 但仍有部分重要樟科植物的进化历史没有涵盖在现有自然保护区范围内; 按照传统方法设定的自然保护区虽能在一定程度上保护樟科物种的进化历史, 但仍然存在与标准化系统发育多样性保护策略相矛盾的地方。因此, 今后在建立自然保护区时, 应将系统发育多样性考虑在内, 以保护生物多样性应对环境变化的潜力。  相似文献   

8.
Habitat loss can trigger cascades of secondary extinctions, changing the organization of interacting assemblages. Until recently, most extinction models in interaction systems had limited ecological realism. Here, we estimate a realistic sequence of species extinctions resulting from habitat loss to assess its impacts on the structure of frugivory networks from the Brazilian Atlantic Forest. We show that realistic and random extinctions led to similar patterns. We also identified a threshold in the response of network structure to habitat loss. When forest cover was reduced to less than 40% of the landscape, network organization changed dramatically. Hence, the number of species being lost, rather than the order of species extinctions, is the key determinant of its impacts on the organization of frugivory networks. We highlight the need to conserve around 40% of forest cover to keep the basic organization of frugivory networks, a threshold already reached at the best‐preserved Brazilian Atlantic Forest bioregion.  相似文献   

9.
The global demand for biofuels in the transport sector may lead to significant biodiversity impacts via multiple human pressures. Biodiversity assessments of biofuels, however, seldom simultaneously address several impact pathways, which can lead to biased comparisons with fossil fuels. The goal of the present study was to quantify the direct influence of habitat loss, water consumption and greenhouse gas (GHG) emissions on potential global species richness loss due to the current production of first‐generation biodiesel from soybean and rapeseed and bioethanol from sugarcane and corn. We found that the global relative species loss due to biofuel production exceeded that of fossil petrol and diesel production in more than 90% of the locations considered. Habitat loss was the dominating stressor with Chinese corn, Brazilian soybean and Brazilian sugarcane having a particularly large biodiversity impact. Spatial variation within countries was high, with 90th percentiles differing by a factor of 9 to 22 between locations. We conclude that displacing fossil fuels with first‐generation biofuels will likely negatively affect global biodiversity, no matter which feedstock is used or where it is produced. Environmental policy may therefore focus on the introduction of other renewable options in the transport sector.  相似文献   

10.
Aim  Anthropogenic habitat loss is usually cited as the most important cause of recent species' extinctions. We ask whether species losses are in fact more closely related to habitat loss than to any other aspect of human activity such as use of agricultural pesticides, or human population density (which reflects urbanization).
Location  Canada.
Methods  We statistically compared areas in Canada where imperiled species currently occur, versus areas where they have been lost. Using multiple regressions, we relate the numbers of species that had suffered range reductions in an ecoregion to variables that represent present habitat loss, pesticide use and human population density.
Results  We find high losses of imperiled species in regions with high proportions of agricultural land cover. However, losses of imperiled species are significantly more strongly related to the proportion of the region treated with agricultural pesticides. The relationship between species losses and area treated with pesticides remains significant after controlling for area in agriculture.
Main conclusions  Our results are consistent with the hypothesis that agricultural pesticide use, or something strongly collinear with it (perhaps intensive agriculture more generally), has contributed significantly to the decline of imperiled species in Canada. Habitat conversion per se may be a less important cause of species declines than how that converted habitat is used.  相似文献   

11.
Habitat loss and the limits to endangered species recovery   总被引:3,自引:0,他引:3  
Canada is one of the last places on earth with extensive wilderness areas, yet the number of Canadian species threatened with extinction continues to rise every year. Using satellite‐derived land use data, we find that habitat loss explains most of the variation in numbers of endangered species across Canada. Habitat loss within species ranges is, therefore, likely to be the leading factor inhibiting their recovery. We measured habitat loss individually within the known ranges of 243 terrestrial species at risk of extinction across Canada. Recovery potential, as measured by extent of natural habitat within each species’ range, is bimodally distributed, but less than 50% of the range of the majority of Canada's species at risk is natural habitat and there is no detectable habitat remaining for 16 of the 243 species at risk. There were no differences in the recovery potential of species categorized either by threat level (special concern, threatened, or endangered) or taxon. Despite having extensive wilderness areas, Canada has similar rates of endangerment to other countries in the Americas, underlining the effect of severe habitat loss to intensive agriculture that has occurred in Canada's most biologically diverse regions. Improvements to protected areas networks and especially cooperative conservation activities with private landowners will do the most to improve the recovery prospects of species at risk in Canada.  相似文献   

12.
Abstract How to maximize the conservation of biodiversity is critical for conservation planning, particularly given rapid habitat loss and global climatic change. The importance of preserving phylogenetic diversity has gained recognition due to its ability to identify some influences of evolutionary history on contemporary patterns of species assemblages that traditional taxonomic richness measures cannot identify. In this study, we evaluate the relationship between taxonomic richness and phylogenetic diversity of angiosperms at genus and species levels and explore the spatial pattern of the residuals of this relationship. We then incorporate data on historical biogeography to understand the process that shaped contemporary floristic assemblages in a global biodiversity hotspot, Yunnan Province, located in southwestern China. We identified a strong correlation between phylogenetic diversity residuals and the biogeographic affinity of the lineages in the extant Yunnan angiosperm flora. Phylogenetic diversity is well correlated with taxonomic richness at both genus and species levels between floras in Yunnan, where two diversity centers of phylogenetic diversity were identified (the northwestern center and the southern center). The northwestern center, with lower phylogenetic diversity than expected based on taxonomic richness, is rich in temperate‐affinity lineages and signifies an area of rapid speciation. The southern center, with higher phylogenetic diversity than predicted by taxonomic richness, contains a higher proportion of lineages with tropical affinity and seems to have experienced high immigration rates. Our results highlight that maximizing phylogenetic diversity with historical interpretation can provide valuable insights into the floristic assemblage of a region and better‐informed decisions can be made to ensure different stages of a region's evolutionary history are preserved.  相似文献   

13.
Understanding the environmental factors driving species‐genetic diversity correlations (SGDCs) is critical for designing appropriate conservation and management strategies to protect biodiversity. Yet, few studies have explored the impact of changing land use patterns on SGDCs specifically in aquatic communities. This study examined patterns of genetic diversity in roach (Rutilus rutilus L.) together with fish species composition across 19 locations in a large river catchment, spanning a gradient in land use. Our findings show significant correlations between some, but not all, species and genetic diversity end points. For example, genetic and species differentiation showed a weak but significant linear relationship across the Thames catchment, but additional diversity measures such as allelic richness and fish population abundance did not. Further examination of patterns in species and genetic diversity indicated that land use intensification has a modest effect on fish diversity compared to the combined influence of geographical isolation and land use intensification. These results indicate that environmental changes in riparian habitats have the potential to amplify shifts in the composition of stream fish communities in poorly connected river stretches. Conservation and management strategies for fish populations should, therefore, focus on enhancing connectivity between river stretches and limit conversion of nearby land to arable or urban use to maintain current levels of biodiversity.  相似文献   

14.
15.
The plant fossil record was reviewed to highlight how consideration of plant carbon balance strengthens our understanding of various evolutionary innovation and extinction events. Following a brief physiological primer to carbon acquisition and allocation in C3‐plants, specific evolutionary events are discussed in connection with postulated carbon‐based mechanisms. Primary topics include: (i) the evolution of plants with the C4‐photosynthetic pathway; (ii) the surprising lack of plant extinctions during the Pleistocene (1.6 million years ago, Ma); (iii) the trend toward declining plant diversity and increasing rates of herbivory across the Palaeocene/Eocene transition (57–52 Ma); and (iv) megaherbivore extinctions at the end of the Pleistocene (10 thousand years ago, Ka). A framework is presented for testing hypotheses on the cause–effect relationships between global carbon cycling, plant carbon dynamics and the evolution of terrestrial ecosystems.  相似文献   

16.
17.
Measures of biodiversity encompass variation along several dimensions such as species richness (SR), phylogenetic diversity (PD) and functional/trait diversity (TD). At the global scale, it is widely recognized that SR and PD are strongly correlated, but the extent to which either tends to capture variation in TD is unclear. Here, we assess relationships among PD, SR and TD for a number of traits both across clades and regional assemblages of mammals. We also contrast results using two different measures of TD, trait variance and a new measure we refer to as trait bin filling (the number of orders of magnitude of variation that contain at least one species). When TD is defined as trait variance, PD is a much stronger correlate of TD than SR across clades, consistent with hypotheses about the conservation value of PD. However, when TD is defined as bin filling, PD and SR show similar correlations with TD across clades and space. We also investigate potential losses of SR, PD and TD if species that are currently threatened were to go extinct, and find that threatened PD is often a similar predictor of threatened TD as SR.  相似文献   

18.
Phylogenetic diversity (PD) represents the evolutionary history of a species assemblage and is a valuable measure of biodiversity because it captures not only species richness but potentially also genetic and functional diversity. Preserving PD could be critical for maintaining the functional integrity of the world's ecosystems, and species extinction will have a large impact on ecosystems in areas where the ecosystem cost per species extinction is high. Here, we show that impacts from global extinctions are linked to spatial location. Using a phylogeny of all mammals, we compare regional losses of PD against a model of random extinction. At regional scales, losses differ dramatically: several biodiversity hotspots in southern Asia and Amazonia will lose an unexpectedly large proportion of PD. Global analyses may therefore underestimate the impacts of extinction on ecosystem processes and function because they occur at finer spatial scales within the context of natural biogeography.  相似文献   

19.
Humans are making increasing demands on natural ecosystems. One recent study has concluded that our species is consuming or diverting some 40% of the net photosynthetic productivity of our planet. Many habitats are being converted to simpler systems which provide more harvestable goods to people. As a result, genetic diversity, species and whole ecosystems are disappearing; some scientists suggest that as many as 25% of the world's species could be lost in the next several decades.The sinking ark is usually characterized in terms of pollution, habitat loss, poaching, introduced species and illegal trade in wildlife products, but these are symptoms rather than causes. At a more fundamental level, many of the same factors which have enabled pollution to become such a problem have also been responsible for the loss in biodiversity; the most important factor is that the effects of pollutants on biodiversity have been considered an externality, an unintended side effect of industrial activity which brought measurable benefits to people. Development activities which have depleted biodiversity have proven profitable only because the real costs have been hidden.Keeping the ark afloat will require the Five-I Approach: investigation (learning how natural systems function); information (ensuring that the facts are available to inform decisions); incentives (using economic tools to help conserve biodiversity); integration (promoting a cross-sectoral approach to conserving biodiversity); and international support (building productive collaboration for conserving biodiversity).  相似文献   

20.
不同土地利用方式对河北坝上步甲物种多样性的影响   总被引:3,自引:0,他引:3  
王建芳  王新谱  李秀敏  刘桂霞 《昆虫学报》2010,53(10):1127-1134
为了探讨土地利用方式对步甲物种多样性的影响及其与环境因子的关系, 于2009年5-10月利用巴氏罐法, 对河北坝上塞北管理区内的灌草丛、马铃薯地、苜蓿地、围封草地、中度放牧草地和重度放牧草地6种生境的步甲进行了系统调查。结果表明: (1)共捕获步甲标本10 804号, 计10属18种, 其中强足通缘步甲Pterostichus fortipes、侧步甲Carabus latreillei和双斑猛步甲Cymindis binotata占优势, 个体数分别占总数的67.5%, 7.53%和7.06%。(2)苜蓿地中的步甲密度、物种丰富度、Margalef丰富度指数、Shannon-Wiener多样性指数和均匀度指数均较高, 其他样地较低。(3)聚类分析结果显示, 不同生境的步甲群落相似性与受干扰强度和土地利用方式一致。(4)步甲主要在6-9月活动, 高峰期为7-8月。各物种在不同土地利用方式生境内的季节变化趋势与不同生境植被生长季节相关, 步甲个体数量随着植物生物量的增加而增加。强足通缘步甲Pterostichus fortipes高峰期大多出现在植物生长旺盛的7月, 仅围封草地内的高峰出现在8月; 双斑猛步甲Cymindis binotata的高峰期出现在8-9月。(5)典范对应分析表明, 土壤含水量、土壤温度、植物盖度、植物生物量及植株高度是影响步甲群落组成的重要环境因子。结论认为, 不同土地利用方式对环境的干扰影响了步甲赖以生存的生境, 进而影响了其物种的组成和数量分布格局。  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号