中国海笔螺科的分布与区系特点

阐述了笔螺科的地理分布和中国海笔螺科的区系特点 ,指出笔螺科大多属热带和亚热带种类。中国海已记录笔螺 73种 ,主要分布于福建、广东、台湾、海南和西沙、南沙群岛。中国海的笔螺科种类在区系组成上属印度 马来区系     

中国海鼓虾科角鼓虾属分类研究(甲壳亚门,十足目)

对中国海鼓虾科角鼓虾属系统分类进行了研究.角鼓虾全世界共记录34种,其中中国海记录了9种.本文中记录中国海分布的角鼓虾属Athanas 8种,其中对中国海2新纪录种A.polymorphus Kemp和A.squillophilus Hayashi,进行了描记,并提供了中国角鼓虾种检索表.在中国的材料中:A.japonicus、A.ohsimai、A.polymorphus及A.squillophilus 4种的螯足表现了多态性,A.ohsimai和A.squillophilus的螯足多态性也是首次发现和记载.所有研究测量标本均保存在中国科学院海洋研究所.     

中国海物种的一般特点

中国海已记录20 278个物种,它们隶属于5个界、44个门,其中,有12个门是海洋特有的。中国海洋的物种比淡水多,比陆地少。物种数由北往南递增。中国海洋的物种有暖水种、温水种和广分布种。许多热带海洋生物分布的北界和一些温带海洋生物分布的的南缘就在中国海域。     

新书介绍

<正> 《中国海菜花属的系统植物学与物种生物学研究》一书,是作者在武汉大学生物系孙祥钟教授指导下所作的博士论文,最近由武汉大学出版社出版发行。这部专著展示了作者从当今植物分类学的两个发展方向——系统植物学与物种生物学——对中国海菜花属植物的研究成果。前半部分属系统植物学范畴。作者以居群概念,利用栽培观察、同工酶电泳、野外居群考察和形态研究等诸方面得到的证据,在数值分类和分支分类研究的基础上,以综合分类学的观点解决了中国海菜花属植物的分类和系统发育问题。     

海洋浮游植物与生物碳汇

系统描述了浮游植物与海洋碳汇相关的几个过程:初级生产、浮游植物沉降、浮游动物粪球打包沉降、经典食物链碳汇、溶解有机碳生产和转化、透明胞外聚合颗粒物(TEP)凝聚网,和CO₂分压升高(海水酸化)影响下浮游植物功能群转变及中国海可能的生物碳汇前景展望。提出海洋初级生产过程和TEP凝聚网过程是中国海生物碳汇的关键过程,而中国海的黄海中部及长江口区域是生物碳汇研究的重点区域,建议将硅藻及其碳汇过程作为今后研究的重点。     

异毛虫科(环节动物门,多毛纲)中国种类记述

系统报道了中国科学院海洋研究所海洋生物标本馆收藏的异毛虫科标本,记述了该科采于中国海域的13种,其中2种为中国海新纪录种,即塔独指虫Aricidea (Acmira) finitina Strelzov,1979和肥美独指虫Aricidea (Allia) pulchra Strelzov,1979,并提供了中国海迄今已发现的异毛虫科18个种的分种检索表.     

中国海菜花属植物的性状分析

本文对中国海菜花属全部已知分类群的84个形态学、生物学和生态学性状,进行了R分析和主成分分析。R分析结果表明,被研究的性状可明显地划分为若干组高度相关的性状,它们或表明本属向次生性陆生和异花传粉方向演化,或具重要的分类价值。主成分分析结果表明,仅前16个主成分几乎可保留84个性状的全部信息量,这说明在中国海菜花属分类研究中所选性状很合理;前3个主成分可保留总信息量的76.56%,说明在三维空间内能较好地反映中国海菜花属所有已知分类群间的相对位置。     

中国海典型生境双壳类软体动物多样性特点

中国海域广阔、海岸线绵长、环境复杂、包含的生境多样,对中国海典型生境中双壳类软体动物多样性的分析,可以反映中国海双壳类软体动物的区系特点.作者根据多年的研究成果和国内外贝类学家的报道,对不同典型生境的双壳类软体动物的多样性特点、生活环境、生态习性进行了阐述,对不同海区的双壳类软体动物的分布特点进行了分析.由于沿岸水、冷...     

中国海毛颚类物种多样性的研究

中国海已记录毛颚类有37种,可分为3个生态类群,即暖水性、暖温性和深水类群。种数是由北往南、由近岸向外海递增。中国海毛颚类可划分暖温带区系、热带- 暖温带混合区系和热带大洋区系。大多数种类广泛分布于印度洋、大西洋和太平洋等水域。     

中国海砂海星科(棘皮动物门,海星纲)种类记述

系统报道了中国海砂海星科的全部种类,计1属9种.提供了分种检索表和各种的鉴别特征、地理分布、外部形态图和地理分布图,并讨论了各种目前存在的分类学问题.     

中国红树林湿地物种多样性及其形成

目前中国红树林湿地共记录了2854种生物,包括真菌136种、放线菌13种、细菌7种、小型藻类441种、大型藻类55种、维管束植物37种、浮游动物109种、底栖动物873种、游泳动物258种、昆虫434种、蜘蛛31种、两栖类13种、爬行类39种、鸟类421种和兽类28种。这些动物中有8种国家一级保护动物,75种二级保护动物。中国红树林湿地是中国濒危生物保存和发展的重要基地,并在跨国鸟类保护中起着重要作用。中国红树林湿地单位面积的物种丰度是海洋平均水平的1766倍。从初级生产物质基础、食物关系多样性、宏观尺度和微观尺度的空间异质性、生境利用的时序性等方面分析了中国红树林湿地物种多样性极其丰富的原因。     

横断山区的蝶类资源与珍稀蝴蝶的保护

横断山区的蝶类561种,隶属于12科,208属.在12科中,种类最多的是蛱蝶科148种,其次是眼蝶科117种,灰蝶科65种,凤蝶科63种,粉蝶科60种,弄蝶科60种,蚬蝶科18种,绢蝶科12种,斑蝶科9种,环蝶科6种,喙蝶科2种,珍蝶科1种.分布于横断山区的珍稀蝴蝶有44种,其中国家Ⅰ级保护的1种,Ⅱ级保护的3种.     

稀有种和常见种对植物群落物种丰富度格局的相对贡献

物种丰富度格局的形成不仅依赖于群落的构建过程, 同样也依赖于群落中的物种组成(如稀有种和常见种)。本文以黄土高原子午岭林区的辽东栎(Quercus wutaishanica)林为研究对象, 根据频度大小对物种进行排序, 形成稀有-常见种和常见-稀有种两条物种序列, 通过逐一添加(去除)物种, 分析引起的总体物种丰富度及其成分(α多样性和β多样性)的变化, 确定稀有种和常见种对物种丰富度格局的相对贡献。结果表明: (1)常见-稀有种序列与群落总体物种丰富度的相关性呈先剧增后平稳的对数增长曲线, 而稀有-常见种序列与群落总体的相关性与前者刚好相反, 呈先平稳后剧增的指数增长曲线; (2) α多样性在常见-稀有种序列中呈明显的对数变化曲线, 而在稀有-常见种序列中呈指数增长曲线; (3)与α多样性变化相反, β多样性在常见-稀有种序列中随物种的进入先迅速降低后逐渐平稳, 而在稀有-常见种序列中先平稳后急剧降低。可以看出, 常见种不仅主导群落的总体物种丰富度格局, 同时也是α多样性和β多样性格局的重要贡献者。因此, 常见种是群落物种丰富度格局的指示者, 也应该是优先保护的物种。     

广西金钟山鸟类保护区鸟类多样性初步研究

本文共记录到金钟山鸟类274种,分别隶属于18目57科,其中陆生鸟类251种,水鸟23种;以留鸟为主,共157种;候鸟、旅鸟分别为104种、13种;东洋种为优势类群,共有171种,古北种和广布种分别为4种、27种。这些鸟类中有国家重点保护鸟类39种,中国特有种鸟类3种,列入世界自然保护联盟红皮书名录中的鸟类5种,列入中国濒危动物红皮书名录中的鸟类20种,列入CITES附录中的鸟类34种。本文还对金钟山鸟类保护区的5种不同生境类型的鸟类种类组成作了比较,结果表明灌丛＋农田的鸟种多样性指数最高,为3．04;水域的鸟种多样性指数最低,为2．14。     

THE MACROEVOLUTIONARY CONSEQUENCES OF ECOLOGICAL DIFFERENCES AMONG SPECIES

Abstract:  In this paper, I examine the dynamics of species richness in a model system in which multiple species compete in a metacommunity (multiple patches linked by dispersal). Patches lie along an environmental gradient, and new species are introduced into the system by speciation of existing species. This model is used to explore how the ecological similarity of species influences the patterns in community structure that result and to determine whether patterns in fossil and systematics data may be signatures for different types of community structure. Making species more similar overall along the entire gradient or making new species that have more similar optimal positions along the gradient to their progenitor both increase the time required to drive species extinction. As a result, making species more similar ecologically to one another increases overall species richness because of an increased frequency of transient species in the system. Having more transient species in systems shifted the longevity distributions of species in the fossil record towards having a greater frequency of shorter duration species, and the age distribution of extant species that would be estimated from molecular phylogenies also had a higher frequency of younger aged species. Comparisons of these results with species longevity distributions extracted from two data sets and with species ages derived from species-level molecular phylogenies strongly suggest that transient species are an important component of real biological communities.     

安徽省两栖爬行动物名录修订

参考两栖爬行动物分类学和分子系统学的最新研究成果, 收集了近年来安徽省两栖爬行类相关的研究资料, 整理成安徽省两栖爬行类物种与分布名录。截止到2018年11月30日, 安徽省共记录两栖动物2目9科26属44种, 其中安徽特有种3种; 爬行动物3目11科48属72种, 其中安徽特有种1种。与《安徽两栖爬行动物志》(1991)相比, 共增加了12种, 删除1个物种, 更改了29个物种的名称。区系分析表明, 东洋界种类91种(78.4%), 古北界种类10种(8.7%), 广布型15种(12.9%)。列入《国家重点保护野生动物名录》的有4种, 列入《中国脊椎动物红色名录》的有112种。     

江西齐云山自然保护区鸟类区系与多样性分析

2006年11月和2007年2～9月,对齐云山保护区的鸟类进行了本底调查和物种监测,共记录到鸟类257种,隶属于17目54科.其中留鸟120种,候鸟(夏候鸟、冬候鸟和旅鸟)137种;古北界种类97种(37.7%),东洋界种类141种(54.9%),广布种有19种(7.4%);国家重点保护鸟类8科34种;发现江西省新纪录鸟类4种.多样性分析结果显示,该区鸟类群落Shannon-Wiener指数、Pielou指数、和Simpson指数分别为3.875、0.791和0.964.从各生境群落多样性指数看,农田居民区中鸟类群落多样性指数最大,其次是灌草丛和阔叶林,溪流水域的多样性指数最小;优势度指数在不同生境的变化趋势与群落多样性指数相似;灌草丛中鸟类群落均匀度指数最高,阔叶林中的鸟类群落均匀度指数最低.通过与周边包括九连山、井冈山、江西武夷山和广东车八岭4个保护区的鸟类进行物种多样性G-F指数对比分析,得出齐云山鸟类多样性与九连山相当,而高于其他3个保护区.     

海南省海口地区龟类市场贸易调查

2002～2004年,对海口地区龟类市场贸易进行了调查。在21个贸易市场共发现龟类23种2572只,其中淡水龟科17种,鳖科4种,陆龟科1种,鳄龟科1种;国外龟类12种,占种数的52％,中国和国外共有龟类11种,占种数的48％;在海南岛分布的龟类有7种,占种数的30％;在23种龟中,10种为濒危物种,1种为易危物种,11种为CITES（2003）附录Ⅱ物种。调查表明,市场上的国外龟类在种类和数量上占绝对优势,一些国家保护龟类也出现在贸易市场上。本文对海口地区龟类市场贸易现状进行了分析和讨论。     

Phylogenetic relationships and climatic adaptations in the Drosophila takahashii and montium species subgroups

We analyze phylogenetic relationships among temperate, subtropical highland, and subtropical lowland species of the Drosophila takahashii and montium species subgroups based on sequence data of COI and Gpdh genes and discuss the evolution of temperate species in these subgroups with reference to their climatic adaptations. In the takahashii subgroup, D. lutescens (the temperate species) branched off first in the tree based on the combined data set, but D. prostipennis (the subtropical highland species) branched off first in the trees based on single genes. Thus, phylogenetic relationships in this subgroup are still ambiguous. In the montium subgroup, the cool-temperate species are phylogenetically close to the warm-temperate species, and these cool- and warm-temperate species form a cluster with the subtropical highland species. This suggests that perhaps the cool-temperate species derived from the warm-temperate species and the warm-temperate species derived from the subtropical highland species. In comparison with the subtropical lowland species, the subtropical highland species may be better able to colonize temperate areas since, as in the temperate species, they have an ability to develop their ovaries at moderately low temperature. However, the subtropical highland species, as well as the subtropical lowland species, were much less cold tolerant than the temperate species. Therefore, considerable genetic reformation would be required for both the subtropical highland and the subtropical lowland species to adapt to temperate climates.     

The rarity concept and the commonness of rarity in freshwater zooplankton

1. Regional distribution, frequency of occurrence and relative abundance were scored in 2467 Norwegian lakes for all the recorded 130 species of crustacean zooplankton. The majority of species were rare in the sense that 65% of species were recorded in fewer than 10% of localities. Only six species were recorded in more than 50% of localities, and the median number of species in a given locality was 14 (i.e. 10% of the total species pool). 2. Abundances of all species were scored according to the fraction of lakes in which they were recorded, their geographical range of distribution, and their numerical abundance. Typically the most rare species were rare by all three criteria, and vice versa for the common species, pointing to rarity as an inherent property of some species. For some species this rarity reflects being on the edge of their distributional range, while for others rarity seems to be a consequence of their life cycle strategies. 3. Some of the truly rare species have high dispersal rates and high colonization abilities, but are rapidly replaced by other species. Others are confined to specific habitats, often highly eutrophic, pointing to highly specialized niche adaptations. 4. A major cause for the few truly common species seems to be the limited number of species that are able to coexist within a given locality, reflecting ‘the ghost of competition past’ and predation pressure. 5. While species composition and species richness may reflect colonization abilities and stochastic events, the presence or absence of species is not only a random lottery but also a consequence of species‐specific attributes.