中国被子植物濒危等级的评估

本文基于文献和标本信息收集以及专家提供的数据,运用IUCN濒危物种红色名录方法首次对中国范围内所有已知被子植物进行灭绝风险评估。结果显示,在评估的30,068种被子植物中,灭绝等级(含灭绝、野外灭绝、地区灭绝)共计40种;受威胁等级(极危、濒危、易危)3,363种,受威胁比例为11.18%。从空间分布看,我国受威胁被子植物主要集中分布在西南地区以及台湾、海南等岛屿,且主要分布在中低海拔地区。对受威胁物种的分析结果表明,包括原生植被破坏在内的生境丧失及破碎化是我国被子植物濒危的首要因子,涉及约84.1%的受威胁物种;过度采挖和物种内在系统问题位列致危因子的第二、三位,分别涉及38%和14%的物种。其他的致危因子包括外来入侵种在内的种间竞争、环境污染、自然灾害和全球气候变化等。一个物种的致危因子往往是多方面的。本次评估与2004年红色名录相比,生境变化、实施保护措施及分类学新修订使一些物种的濒危等级发生了变化,这也印证了红色名录是一个动态的系统,需要根据最新信息进行更新,以便为生物多样性保护提供实时准确的基础数据。     

通过红色名录评估探讨中国爬行动物受威胁现状及原因

为了评估中国爬行动物红色名录, 我们按照爬行动物生物学特性, 适当修改了IUCN濒危物种红色名录标准Version 3.1。在此基础上, 评估了中国爬行动物生存现状, 参与编制了《中国生物多样性红色名录——脊椎动物卷》。此次评估的中国爬行动物有3目32科133属461种, 结果为: 区域灭绝(RE) 2种、极危(CR) 34种、濒危(EN) 37种、易危(VU) 66种、近危(NT) 78种、无危(LC) 175种以及数据缺乏(DD) 69种。中国受威胁(包括极危、濒危、易危)的爬行动物共计137种, 约占总数的29.72%, 包括龟鳖目31种、有鳞目蛇亚目67种、蜥蜴亚目38种和鳄形目1种, 高于2014年《IUCN濒危物种红色名录》评估的世界爬行动物受威胁比例(13.61%)。在所有受威胁物种中, 受威胁比例最高的类群是鳄形目(100%)和龟鳖目(91.18%), 其次是有鳞目蛇亚目(28.39%), 第三是有鳞目蜥蜴亚目(20.21%)。中国爬行动物特有种受威胁物种有39种, 占特有种总数(143种)的27.27%, 占受威胁物种总数(137)的28.47%。长江以南的华南和西南地区受威胁的物种最多。爬行动物受人类干扰严重, 主要表现为: 栖息地质量退化及生境破碎化、过度利用及污染和气候变化等。尽管自1989年《中华人民共和国野生动物保护法》实施以来, 一些中国濒危爬行动物的生存状况得到改善。但鉴于中国爬行动物区系的独特性和多样性、地形地貌的复杂性及社会经济发展的不均衡性, 为了维持区域生态安全和资源可持续利用, 拯救中国濒危爬行动物, 尤其是中国特有爬行动物中的极危物种, 是中国动物保护工作最迫切的任务之一。     

通过红色名录评估研究中国哺乳动物受威胁现状及其原因

依据中国哺乳类野生种群与生境现状, 我们利用IUCN Red List Categories and Criteria (Version 3.1), Guidelines for Using the IUCN Red List Categories and Criteria和Guidelines for Application of IUCN Red List Criteria at Regional and National Levels (Version 4.0), 评价了中国所有已知的673种哺乳动物的濒危状况。本次评估了71种《IUCN濒危物种红色名录(2015)》没有评估的哺乳动物, 还评估了60种《IUCN濒危物种红色名录(2015)》误认为中国没有分布的哺乳动物。发现中国有3种哺乳动物“野外灭绝”, 3种“区域灭绝”。受威胁中国哺乳动物共计178种, 约占评估物种总数的26.4%, 高于IUCN濒危物种红色名录的物种平均受威胁率(21.8%)。中国哺乳动物1/4的特有种属于受威胁物种。受威胁比例最高的目是灵长目、食肉目与鲸偶蹄目。多数省区的受威胁哺乳动物物种占本省区哺乳动物总数的20-30%。中国哺乳动物种类多分布在中国第二级地理阶梯。生活在高海拔地区的哺乳动物虽然种类少, 但是受威胁哺乳动物的种类比例高。过度利用、生境丧失和人类干扰名列受威胁哺乳动物致危因子的前3位。自从1989年《中华人民共和国野生动物保护法》实施以来, 一些中国濒危哺乳动物的生存状况得到了改善。然而, 鉴于中国哺乳动物区系的独特性和多样性, 以及中国地形地貌的复杂性, 如何拯救这些濒危物种仍是中国生物多样性保护的一项艰巨任务。     

生物多样性保护优先区对重庆苔藓植物多样性保护的重要性

生物多样性保护优先区的生物多样性十分丰富, 对于生物多样性保护具有重要意义。本文基于野外调查数据和文献资料, 整合大巴山和武陵山两个中国生物多样性保护优先区重庆境内的苔藓植物名录, 通过分析物种丰富度、中国特有种和受威胁物种, 比较了这两个地区的苔藓植物组成特点和相似性。结果显示, 两个保护优先区重庆境内共有苔藓植物77科221属722种, 其物种数分别占重庆市和中国苔藓植物总种数的76.0%和23.9%。两个区域分布有中国特有苔藓植物56种, 占中国苔藓植物总种数的1.9%; 分布有极危苔藓植物1种、濒危4种和易危3种。科、属、种的Jaccard相似性系数分别为0.7、0.6和0.3, 表明两个区域物种组成差异较大。大巴山和武陵山两个中国生物多样性保护优先区都具有较高的苔藓植物物种多样性, 其种类组成具有一定代表性, 对重庆市和中国苔藓植物多样性保护具有重要价值。     

中国两栖动物受威胁现状评估

为了了解我国两栖动物受威胁现状和致危因素, 进而制定相关的保护措施和开展国际合作, 本文依据中国两栖动物野生种群与生境现状, 利用《IUCN物种红色名录濒危等级和标准》(3.1版)和《IUCN物种红色名录标准在国家或地区的应用指南》(4.0版), 对中国已知的408种两栖动物的濒危状况进行了评估, 并编制了《中国两栖动物红色名录》。评估结果表明: 中国两栖动物有1种灭绝, 1种区域灭绝, 受威胁的两栖动物共计176种, 占评估物种总数的43.1%, 明显高于《IUCN濒危物种红色名录》(2015)的物种受威胁率(30.8%)。中国两栖动物特有种272种, 其中48.9%属于受威胁物种。中国两栖动物受威胁比例最高的目是有尾目(63.4%), 明显高于无尾目(39.0%); 受威胁比例最高的科是隐鳃鲵科(Cryptobranchidae) (仅有1种, 100%受威胁), 小鲵科(Hynobiidae) (86.7%)和叉舌蛙科(Dicroglossidae) (78.1%)。有11个省区的受威胁物种数占本省区两栖动物物种总数的30%及以上, 前3位分别是四川(40.8%)、广西(39.2%)和云南(37%)。中国大多数两栖动物物种分布在西南山地和华南地区, 以海拔2,000 m以下区域为主。栖息地退化或丧失、捕捉、环境污染列受威胁两栖动物致危因子的前3位。鉴于中国两栖动物区系的复杂性和独特性, 进一步加强两栖动物资源调查、种群和生境监测及相关科学研究, 仍是今后一段时期开展两栖动物多样性保护和濒危物种拯救行动的关键性基础工作。     

中国非地衣型大型子囊菌受威胁现状评估及致危因素

2018年5月22日是第25个国际生物多样性日, 生态环境部和中国科学院联合发布了《中国生物多样性红色名录——大型真菌卷》。子囊菌是真菌界物种数量最丰富的类群, 其中小型种类居多, 此次参评的我国非地衣型大型子囊菌(以下简称“大型子囊菌”)包括870种。评估结果表明, 我国大型子囊菌受威胁物种有24种, 其中疑似灭绝1种、极危6种、濒危3种、易危14种, 受威胁物种占评估大型子囊菌物种数的2.76%。此外, 无危的大型子囊菌189种, 占评估物种数的21.72%, 数据不足的616种, 占评估物种数的70.80%。本文对中国大型子囊菌红色名录评估的方法、过程和评估结果等进行了介绍, 对其受威胁现状、受威胁物种的区域分布、致危因素等进行了总结分析, 并提出了相应的保护措施和建议。分类学研究是进行红色名录评估的基础, 在未来相当长的一段时间里, 真菌资源调查和分类学研究仍然需要引起重视并投入资金。建议分类学工作者、保护区管理人员、业余爱好者群体和生态学家合作并广泛参与大型真菌受威胁状况的评估。     

基于能值的陆域受威胁和濒危物种价值估算——以福建省厦门市为例

开展受威胁和濒危物种价值评估是生物多样性研究的关键问题之一。当前受威胁和濒危物种研究正处于濒危等级界定和保护优先性确定阶段,存在不同保护等级交叉管理、价值评估方法欠缺及重复性计算等多方面问题。利用IUCN濒危等级和中国特有种等级名录确定厦门市不同濒危等级物种数,在此基础上利用能值转换率和修正的中国能值/货币比率对厦门市陆域受威胁和濒危物种价值进行估算。结果显示,通过多途径整理纳入估算的厦门市陆域野生动植物物种数为1444种,其中受威胁和濒危物种数为318种;2015年厦门市物种能值价值约为3.53×10~(11)元,2010年约为3.08×10~(11)元,其中两期受威胁和濒危物种能值价值均占物种总价值的88.31%;中国特有种等级对价值贡献最大达73.25%,其次是IUCN濒危等级达23.24%。研究表明,能值评估法能够客观凸显受威胁和濒危物种价值,研究结果可为生物多样性及物种保育的管理决策提供技术支撑。     

国家重点保护野生植物受威胁等级的评估

物种受威胁等级的评估是确定物种优先保护顺序和制订濒危物种保护策略的重要依据,是生物多样性保护工作中的一个重要步骤.本研究以<国家重点保护野生植物名录>所列物种(包括即将发布的物种)为评估对象,采用IUCN红色名录受威胁等级和标准,从全国尺度上对我国重点保护野生植物的受威胁等级进行了评估.评估结果为:绝灭(EX)2种,野外绝灭(EW)3种,极危(CR)310种,濒危(EN)638种,易危(VU)911种,近危(NT)117种,无危(LC)162种,数据缺乏(DD)34种.将评估结果与国家Ⅰ、Ⅱ保护级别进行对比,发现两者之间存在较为明显的不一致性,其原因是物种的受威胁程度并不是确定受保护物种以及划分保护级别的唯一依据.该研究为建立我国重点保护野生植物受威胁等级体系、实施有效的保护策略提供了科学参考.     

黄河流域淡水鱼类多样性和保护

本文介绍了黄河流域鱼类研究的历史、淡水鱼类的物种组成、整体分布格局、特有性、濒危性, 以及鱼类多样性在黄河上、中、下游等的特点。历史上对于黄河鱼类多样性的研究, 历经了四个阶段, 从最初的零星记录一直到现阶段的深入研究。综合历史记录和野外调查, 已知黄河流域分布的淡水鱼类共计147种, 隶属于12目21科78属, 其中鲤形目种类占据绝对优势。另外, 全流域黄河特有种计有27种, 受危物种24种, 分别占总数的18.37%和16.32%。同中国主要江河相比, 黄河鱼类在高级分类阶元上的多样性较高, 但物种多样性则处在较低水平; 尽管黄河特有鱼类和受危物种比例低于全国平均水平, 但上游特有鱼类和珍稀濒危鱼类的占比很高。目前黄河鱼类多样性大幅降低, 现状调查仅能采获历史记录种类的53.06%。梯级水电开发、水资源过度利用、外来物种、水域污染和过度捕捞都是威胁鱼类多样性的重要因素, 但对各河段和支流的影响不一, 应做出有针对性的保护部署。     

中国大型担子菌受威胁现状评估

基于文献和标本信息以及专家提供的数据, 依据中国大型真菌评估的标准和程序, 对中国范围内已知大型担子菌进行了受威胁状态评估。结果显示, 在评估的6,268种担子菌中, 受威胁(疑似灭绝、极危、濒危、易危)的物种有45种, 受威胁比例为0.72%。受威胁的大型担子菌物种中食药用菌比例达1/3以上, 且大部分物种仍无法人工栽培, 主要依赖野生资源。我国受威胁担子菌主要集中分布在西南和东北地区。人类活动导致的物种栖息地萎缩和破坏是我国大型担子菌受威胁的首要因子, 过度采挖是食药用菌受威胁的重要原因。此外, 数据不足的大型担子菌共4,251种, 占被评估大型担子菌总数的67.82%, 表明我国大型担子菌物种多样性及相关研究还存在不足。     

黄河流域鸟类多样性现状、分布格局及保护空缺

黄河流域幅员辽阔, 多样的地理气候、植被类型及人类活动塑造了多样化的生物多样性格局。本研究以IUCN与国际鸟盟发布的鸟类分布图层为基础, 同时收集了黄河流域2009-2019年的鸟类实地观测记录, 包括观鸟记录、GBIF数据库、红外相机监测及其他实地调查的鸟类数据, 共得到35,026条鸟类实地观测有效记录。汇总结果显示, 黄河流域记录有鸟类物种662种, 占中国鸟类物种总数的45.81%。这些鸟类分属于23目83科, 其中雀形目物种数最多(384种, 占本目全国鸟种总数的46.83%), 其次为鸻形目(67种, 占50.00%)和雁形目(39种, 占72.22%)。黄河流域受威胁鸟类共计121种, 其中有37种和52种分别在IUCN红色名录和《中国脊椎动物红色名录》中被列为受威胁物种(即评估级别为极危、濒危或易危), 22种和73种被分别列为国家I级和II级重点保护野生动物。这些受威胁鸟种多为地栖性、体型大、营养级高或具有长距离迁徙习性的物种。黄河流域鸟类整体物种多样性由南向北递减, 以黄河上中游四川、甘肃、陕西的高原与山地内鸟种最为丰富, 而受威胁鸟类物种多样性热点区则在黄河中下游, 下游黄河三角洲及邻近平原区为受威胁鸟类最主要集中分布区。黄河流域内48个国家级自然保护区共覆盖鸟种数504种(占黄河流域鸟类总种数的76.13%), 其中受威胁鸟种92种(占黄河流域受威胁鸟种数的76.03%)。区域内国家级自然保护区大多分布在黄河上游, 对黄河下游的受威胁物种覆盖程度较低, 保护空缺较严重。对此, 我们建议着重加强中下游自然保护区建设与能力提升, 增加对中下游受威胁鸟种的保护力度, 在保护策略上应当积极探索高强度土地利用下的多样化保护机制。     

Phylogenetic Patterns of Extinction Risk in the Eastern Arc Ecosystems,an African Biodiversity Hotspot

There is an urgent need to reduce drastically the rate at which biodiversity is declining worldwide. Phylogenetic methods are increasingly being recognised as providing a useful framework for predicting future losses, and guiding efforts for pre-emptive conservation actions. In this study, we used a reconstructed phylogenetic tree of angiosperm species of the Eastern Arc Mountains – an important African biodiversity hotspot – and described the distribution of extinction risk across taxonomic ranks and phylogeny. We provide evidence for both taxonomic and phylogenetic selectivity in extinction risk. However, we found that selectivity varies with IUCN extinction risk category. Vulnerable species are more closely related than expected by chance, whereas endangered and critically endangered species are not significantly clustered on the phylogeny. We suggest that the general observation for taxonomic and phylogenetic selectivity (i.e. phylogenetic signal, the tendency of closely related species to share similar traits) in extinction risks is therefore largely driven by vulnerable species, and not necessarily the most highly threatened. We also used information on altitudinal distribution and climate to generate a predictive model of at-risk species richness, and found that greater threatened species richness is found at higher altitude, allowing for more informed conservation decision making. Our results indicate that evolutionary history can help predict plant susceptibility to extinction threats in the hyper-diverse but woefully-understudied Eastern Arc Mountains, and illustrate the contribution of phylogenetic approaches in conserving African floristic biodiversity where detailed ecological and evolutionary data are often lacking.     

The center of the center of marine shore fish biodiversity: the Philippine Islands

Synopsis Multiple datasets show global maxima of marine biodiversity in the Indo–Malay–Philippines archipelago (IMPA). Analysis of distribution data for 2983 species reveals a pattern of richness on a finer scale and identifies a peak of marine biodiversity in the central Philippine Islands and a secondary peak between peninsular Malaysia and Sumatra. This pattern is repeated in diverse habitat and higher taxa classes, most rigorously for marine shore fishes, supporting geohistorical hypotheses as the most general unifying explanations. Specific predictions based on area of overlap, area of accumulation, and area of refuge hypotheses suggest that present day eastern Indonesia, or Wallacea, should be the center of marine biodiversity. Processes suggested by these three hypotheses contribute to the diversity in this region and are also a likely explanation for the secondary center of diversity. Our study indicates, however, that there is a higher concentration of species per unit area in the Philippines than anywhere in Indonesia, including Wallacea. The Philippine center of diversity is consistent with hypotheses that this area experienced numerous vicariant and island integration events and these hypotheses warrant further testing. Special attention to marine conservation efforts in the Philippines is justified because of the identification of it as an epicenter of biodiversity and evolution.     

Exploitation-related reef fish species richness depletion in the epicenter of marine biodiversity

The central Visayan region of the Philippines historically has the highest concentration of coral reef fishes than any other large marine area in the world. This well-supported biogeographic phenomenon is contradicted by recent transect observations on coral reefs that indicates that the Visayan region and the southern Philippine Sea region have the lowest species richness in the Philippines. The Visayan region has unusually low counts of species typically exploited in fisheries and the aquarium trade. This evidence, coupled with numerous reports of intense fishing and habitat degradation and subsequent species declines at local scales suggests that this exploitation is having a cumulative effect on the overall species richness of the Visayan region. Successes in Marine Protected Areas in this region in increasing species richness at local scales suggests that improved management of these protected areas coupled with much more intensive fisheries management will be key to reviving a healthy biodiversity in the Visayas.     

云南被子植物蔷薇分支的进化历史研究

本文以云南被子植物蔷薇分支为研究对象,基于物种间的演化关系,结合其地理分布,从进化历史的角度探讨了物种、特有种、受威胁物种的种类组成及系统发育组成的分布格局,并整合自然保护地的空间分布,对生物多样性的重点保护区域进行识别。结果显示：云南被子植物蔷薇分支的物种密度与系统发育多样性、特有种密度、受威胁物种密度均呈显著正相关,云南南部和西北部是物种丰富度与系统发育多样性最为丰富的区域;就云南整体而言,蔷薇分支的标准化系统发育多样性较低;云南南部、东南部、西北部是蔷薇分支的重点保护区域。     

云南被子植物菊类分支的系统发育多样性及其分布格局

全球气候变化与人为活动等因素导致的生物多样性丧失,引起了全球各界对生物多样性保护的高度关注。传统生物多样性保护主要对物种、特有种、受威胁物种的种类组成及其分布模式开展研究,忽视了进化历史在生物多样性保护中的作用。云南是全球生物多样性热点地区的交汇区,生物多样性的保护历来受到广泛关注,为了更好地探讨云南生物多样性的保护措施,该研究以云南被子植物菊类分支物种为研究对象,基于物种间的演化关系,结合其地理分布,从进化历史的角度探讨物种、特有种、受威胁物种的种类组成及系统发育组成的分布格局,并整合自然保护地的空间分布,识别生物多样性的重点保护区域。结果表明：云南被子植物菊类分支的物种、特有种及受威胁物种的物种密度与系统发育多样性均显著正相关;通过零模型分析发现,由南向北标准化系统发育多样性逐渐降低;云南南部、东南部、西北部是云南被子植物菊类分支的重点保护区域,加强这些区域的保护,将最大化地保护生物多样性的进化历史和进化潜能。由此可见,融合进化历史信息的植物多样性格局分析不仅有助于更加深入地理解植物多样性的形成与演变,也为生物多样性保护策略的制定提供更多的思路。     

Tropical dry forests in New Caledonia

Tropical dry forest is the most endangered major vegetation type in the New Caledonia biodiversity hotspot. Vegetation surveys following a transect method used by Gentry were undertaken in two tropical dry forest sites, Ouen-Toro and Pindai, in order to compare species richness, floristic composition, and structure. Pindai contained significantly higher species richness than Ouen-Toro, although there was little difference in forest structure. Tropical dry forest sites in New Caledonia were compared to seven other biodiversity hotspots with tropical dry forest where Gentry's transect method was employed. New Caledonia and other tropical dry forests on islands contain significantly lower species richness than mainland tropical dry forests in biodiversity hotspots. However, New Caledonia contained the highest number of threatened species based on IUCN global conservation categories. Tropical dry forest in New Caledonia appears to be the world's most endangered tropical dry forest based on the extent of forest, number of reserves, and threatened species. Management of tropical dry forests on private and community lands is absolutely imperative to the long-term persistence of this ecosystem.     

Vascular Plant Species Inventory of a Philippine Lowland Rain Forest and its Conservation Value

The Philippines are one of the most important biodiveristy hotspots on earth. Due to the extraordinary rate of environmental destruction, leaving only 3% of the land with primary forest, this biodiversity is at high risk. Despite that situation information on Philippine forest vegetation is fragmentary and focused on trees. This study aimed at analysing forest remnants in the Leyte Cordillera on the Island of Leyte, and at evaluating their role as refuge to the largely destroyed lowland forest vegetation. A total of 49 plots (100 m² each) between 55 and 520 m a.s.l. were studied. All vascular plant species except epiphytes were included. Records include 685 taxa from 289 genera and 111 families, representing nearly 8% of the known Philippine vascular plant species. More than half (52%) of the species are Philippine endemics. A number of 41 tree species, or 6% of all taxa recorded, are included in the IUCN red list, either as vulnerable, endangered, or critically endangered. Life form composition was dominated by phanerophytes (65.3%), followed by lianas and chamaephytes (17.1 and 16.9%, respectively). The most common families were the Rubiaceae with 35 and the Euphorbiaceae with 32 species. All five Philippine dipterocarp forest types as well as the molave forest type were represented by typical tree species. The area provides an important gene bank of the highly threatened Philippine lowland forest vegetation and is of high value for biodiversity conservation. Additionally, it can play an important role as seed source of valuable tree species for the increasing initiatives to rehabilitate and reforest degraded land with native species.     

Integrating spatially explicit habitat projections into extinction risk assessments: a reassessment of Amazonian avifauna incorporating projected deforestation

Aim We aimed to complete the first systematic assessment of extinction risk based on projected population declines derived from spatially explicit habitat projections for any taxonomic group at a regional scale, to use the outputs to ascertain the efficacy of an existing protected area network in covering species of conservation concern, and identify gaps therein. Location This study focused on Amazonia; an area of exceptional biodiversity, currently experiencing the highest absolute rate of forest loss globally but where the proportion of species assessed as ‘threatened’ on the International Union for the Conservation of Nature (IUCN) Red List in the region is below global averages. Methods For all forest‐dependent Amazonian bird species (814), we revised extinction risk estimates by combining data from a spatially explicit deforestation model with generation length estimates. By overlaying distribution maps for these revised threatened species, we identified crisis areas (areas of projected deforestation supporting the highest numbers of threatened species), refugia (areas projected to retain forest supporting the highest numbers of threatened species) and areas of high irreplaceability: short‐ and long‐term priorities for new protected areas (PAs). Results The number of species qualifying as threatened rose substantially from 24 (3%) to 64–92 (8–11%). Areas of particular concern are the crisis and highly irreplaceable areas within the ‘arc of deforestation’ in the southern Brazilian Amazon states of Rondônia, Mato Grosso and Pará. Main conclusions Through a novel application of the IUCN Red List criteria, we present a spatially accurate rendering of the extinction risks of Amazonian birds. Important areas in the Amazon are not secure. We identify priorities for expansion of the PAs network and key locations where protection should be enforced. We recommend a collaborative approach employing our methods to repeat this process for other taxonomic groups.