大巴山自然保护区种子植物中国特有属的初步研究

大巴山自然保护区分布中国特有属45属,占本区的种子植物总属的4.98%。本区分布的中国种子植物特有属中均为少种属或单种属,单种属22属,少种属23属,分别占本区中国特有属总属数的48.9% 和51.1%。木本属22属,草本属23属,分别占本区中国特有属总属数的48.9% 和51.1%。本区的中国特有属植物主要分布在低山和中山,其中分布在低山的有6属,占总属数的13.3%, 分布在中山的有39属,占总属数的86.7%。其特点表现为众多的古特有属、较明显的过渡性质和丰富的珍稀物种,与四川和湖北的共有成分最多,是中国特有属川东鄂西特有现象中心的重要组成部分。     

武汉东湖水生植物区系四十年间的变化与分析

本文根据作者近年的研究结果,并结合前人的有关研究资料,对东湖四十年间（１９５４－１９９４）水生植物区系组成变化进行了讨论。文中分析了东湖水生植物区系组成、东湖水生植物在中国与世界水生植物区系中的位置、东湖水生植物种属的分布区类型、单种属和寡种属的地理分布格局、东湖水生植物区系的性质、东湖与１０个湖泊水生植物种属相似性的分析。最后对东湖水生植物分类群及种类变化进行了探讨。     

太白山植物区系的特征

太白山为中国中部的最高山峰,它的顶点海拔3767.2米。太白山植物种类丰富,有种子植物120科,627属,1770种(包括种下等级),其中含世界性的单种属22个,少种属60个,中国特有属22个,这些属大部份是古老的科属和孑遗种类。它的地理位置是在中国—日本和中国—喜马拉雅两个植物亚区的分界线上,也是华北、华中和横断山脉三个植物省的交汇处。     

山茶科特有珍稀植物圆籽荷的生物学特性及保护生物学研究

圆籽荷是中国特有的单种属稀有植物,历年来对其研究较少。该文对圆籽荷的分布现状,生境进行了调查,对其物候、形态特征、繁殖过程等生物学特性进行了初步研究。     

神农架维管植物区系初步研究

本文为神农架维管植物区系的初步研究结果,扼要报道了本区系现知的2638种(包括种下等级),分隶193科850属;粗略分析了850属的分布区类型,表明本区系以温带分布特别是北温带分布为主要成份的性质;介绍了本区系一些主要的古老属种,世界单种属47属,在中国为单种属的有33属,分布于该地区的中国特有属43属及中国列入珍稀保护植物49种。通过对木本植物的统计(有99科290属1103种,其中乔木属128属),显示出该地区是中国北温带木本植物,特别是乔木属种最丰富的地区之一。     

海南岛坝王岭热带山地雨林陆均松-线枝蒲桃群系的区系特点

初步探讨了海南坝王岭自然保护区热带山地雨林的代表群落类型即陆均松－线枝蒲桃群系的种子植物区系组成及其地理分布特点。此群落含有61科、137属、326种,热带分布特别是热带－亚洲分布的成分占有明显优势,其次是泛热带分布,热带性很强,中国特有的分布的种属所占比例极低。单、寡种属极为丰富是该地区植物区系组成的另一特点。     

秦岭田峪河流域种子植物区系研究

田峪河流域是陕西秦岭植物园的核心区,有种子植物128科,605属,1231种（不含种下等级）。区系分析表明,该流域仍以温带成分为主,占总属的70.96%,热带成分占21.13%,地中海与中亚成分占4.41%,中国特有属占3.5%,稀有濒危植物、单种属和少种属、中国特有属及木本植物均占较大比重,说明了历史起源的古老性,地理成分复杂,联系广泛,分布交错,具有明显的温带特征。     

陕西省汉中地区中国种子植物特有属的分析

汉中地区种子植物区系自然分布有中国特有属48属,隶属于33科,包括裸子植物1属,被子植物47属,其中单种属24属,少种属18属,多种属6属,从其生活习性上看,木本习性有25属,草本习性的有23属。本文主要分析了汉中地区分布的中国种子植物特有属的地理分布及特点,分析结果表明：其特点主要为显著的温带性质,众多的特有属和丰富的珍稀濒危物种,在地理分布上与华中,西南地区联系密切。     

安徽天堂寨保护植物香果树群落现状分析

香果树(Emm enopterys henryiO liv.)是中国特有单种属孑遗植物,对茜草科(Rub iaceae)系统发育和中国南部及西南部的植物区系研究具有一定意义。香果树不但材质优良,可供建筑及家具等用;而且树形优美,花大而艳丽,极具观赏价值。由于毁林开荒和乱砍滥伐,加上其种子萌发率低,天然     

粉黛佳人——蝟实

蝟实(Kolkwitzia amabilis Graebn.)为忍冬科(Caprifoliaceae)蝟实属(Kolkwitzia)植物,多年生小灌木,为中国特有的单种属珍稀植物[1],常生于海拔300～1 340 m的阳坡或半阳坡,在土层薄、岩石裸露的阳坡亦能正常生长[2].     

稀有濒危植物珊瑚菜的染色体特征及其演化地位

首次分析了珊瑚菜（ Ｇｌｅｈｎｉａ ｌｉｔｔｏｒａｌｉｓ） 根尖体细胞染色体组型。其核型公式为２ ｎ ＝ ２２＝ １８Ｍ ＋ ４Ｓｍ （２Ｓａｔ） , 核型不对称性属于２Ａ 型。据此讨论了该属在我国伞形科稀有濒危单型属和当归亚族中的演化地位。     

滇西南四个自然保护区鱼类多样性及评价指标探究

为了解滇西南怒江水系的南滚河自然保护区、南捧河自然保护区、永德大雪山自然保护区及澜沧江水系的澜沧江自然保护区鱼类多样性和变化趋势, 探讨其差异和变化的原因, 本文采用β多样性指数分析了4个保护区的鱼类多样性, 并比较了鱼类分类阶元的特有性、单型性和古老成分的有无等多项指标。结果显示, 4个自然保护区共有土著鱼类85种, 隶属于6目13科45属。在中国仅见于怒江水系的4个特有属有异鲴属(Aspidoparia)和新条鳅属(Neonoemacheilus)分布于这3个保护区中; 18种特有种中, 仅分布在这3个保护区的狭域特有种5种。在中国仅分布于澜沧江水系的属有31个, 但仅安巴沙鳅属(Ambastaia)分布于澜沧江保护区; 在澜沧江保护区分布着中国仅见于澜沧江水系的特有种20种, 其中狭域特有种3种。怒江水系的3个保护区分布有1个单型属, 即鳗鲡属(Anguilla), 但没有单型种; 澜沧江自然保护区无单型属与单型种分布。4个保护区中的鱼类均系晚第三纪和第四纪形成的种类或类群, 没有古老或孑遗种类。β多样性结果显示, 在4个保护区中澜沧江自然保护区的鱼类多样性最丰富, 而南滚河自然保护区的丰富程度最低, 但是怒江水系3个自然保护区鱼类多样性的代表性及保护地位比澜沧江自然保护区的要高。而特有阶元和单型性阶元的存在体现出怒江水系3个自然保护区的保护价值及保护意义比澜沧江保护区高。地理范围跨度大小、生境空间异质性高低、保护区面积大小及支流多少等是影响鱼类多样性的主要因素。因此, 规划和设计保护区时, 如果能在水系的上、中、下游分别规划1条一级支流作为保护区, 可使该水系的绝大多数鱼类得到保护。     

Diagnosis and relationships of the myrmicine ant genus Ishakidris gen.n. (Hymenoptera: Formicidae)

Abstract. The ant genus lshakidris from Sarawak is described as new. Its relationships with the Brasilian monotypic genus Phalacromyrmex Kempf and the Malagasy monotypic genus Pilotrochus Brown are discussed, and the Phalacromyrmex genus-group is established to hold the three genera. The resemblances of lshakidris to the smithistrumiform dacetine genus Glamymmyrmex Wheeler and the agroecomyrmecine genus Tatuidris Brown & Kempf are discussed and the similarities are analysed as the results of convergence in the characters concerned.     

Phylogenetic diversity and ecological features in the Egyptian flora

Until fairly recently, regional-scale ecological and evolutionarypatterns have tended to be ignored as conservation efforts have been concernedwith species and their habitats. Here we compare frequencies in the Egyptianflora of particular rank sizes (order, family and genus) with patterns ofspecies abundance (classified as very rare, rare, common, or very common) and anarray of life-history attributes. The angiosperm flora of Egypt is representedby 2446 taxa (2088 species), including taxa in 10 subclasses, 51 orders, 120families, and 742 genera. A high degree of monotypism was observed: four ordersare monotypic (each existing as single species), and have very rare overallabundances; 30 families are monotypic (17 of which are very rare or rare); and 354genera are monotypic (over 70% of which are very rare or rare). Fourteenfamilies (in particular the Resedaceae and Zygophyllaceae) have at leastone-fifth of their global species represented in the Egyptian flora. Introducedspecies in general, and tree, aquatic herb and liana life forms all are especially well represented among monotypic genera. Native taxa are highlyrepresented among rare and very rare abundance classes, while introduced taxadid not differ significantly in their abundance patterns, compared to overallflora values. Few large genera (>20 spp.) occur in the flora, with mostspecies concentrated in genera containing 8–19 species per genus.Similarly, few families were highly speciose. Annual and herbaceous species weresignificantly over-represented, mainly among large, speciose genera andfamilies. However, perennials, trees, shrubs, aquatic herbs, lianas and parasiticspecies were found mainly in families and genera having very few taxa.Life-history attributes may have important implications to speciation rates.Taxonomically based results, involving abundances and life-history attributes,are discussed in the context of biodiversity and conservation.     

A revision of the dinocarsiine Encyrtidae with a study of the genus Pelmatencyrtus De Santis (Hymenoptera: Chalcidoidea)

This paper constitutes a revisionary treatment of the Encyrtid subtribe Dinocarsiina as defined by Kerrich (1967). The genera there listed are studied, together with Praleurocerus Agarwal and Aeptencyrtus De Santis, which are here included. Encyrtolophus De Santis is treated as a subgenus of Chrysoplatycerus Ashmead although it is very distinct from the type species of that genus. A new genus is proposed for Tropidophryne flandersi Compare. All specíes are redescribed with exception of two belonging to monotypic genera. Five species are described as new.     

Areography of the Gymnosperms of China (1) Distribution of the Pinaceae of China

Nine of 10 genera and 119 of approximately 240 species of the Pinaceae occur in China, including 67 endemic species and two endemic genera. In this paper, the distributional maps of all the genera of the Pinaceae are presented (fig. 1-8). The horizontal and vertical distributions of species in each genus are discussed. The analysis of the distribution patterns of the genera indicates that some genera, such as Keteleeria, Tsuga, Pseudotsuga, Cathaya and Pseudolarix, are restricted to the area south of the Qinling Mountains and the Huaihe River, and the others, i. e. Picea, Abies, Larix and Pinus, extend northward to northeastern China. However, all of the genera except Keteleeria and Pinus are not found in very dry areas and tropical mountainous regions of China. The monotypic genera, Cathaya and Pseudolarix, are distributed in eastern and central China. The genus Keteleeria consists of 10 species, 7 of which are concentrated in southern Guizhou, northern Guangxi, southwestern Hunan and easternmost Yunnan. The distribution of the remaining 6 genera shows the maximum concentration in western Sichuan and northwestern Yunnan. (Figs. 2-8). Furthermore, more than third of species of the Pinaceae (37.8%) are also concentrated in western Sichuan and northwestern Yunnan. where a great variety of habitats and different topographic features occur. It is apparent that to conduct our systematic and evolutionary studies on this family in these region is especially needed. The relations between the areal size and the tolerance of species are discussed. The distributions of macrofossils and microfossils of the genera of the Pinaceae ia China are given, and it has been proved that areas of most genera of the family were considerably larger in the past. than at present.     

Archakebia—A New Genus of Lardizabalaceae from China

The monotypic genus Archakebia from China is described as new．The genus shares many characters with members of the genus Akebia,except sepals 6,lanceolate or linear,which are common in members of the genus Stauntonia．     

长萼木通属——木通科一新属

缺瓣牛姆瓜Holboellia apetala Q．Xia,J．Z.Suen et Z．X．Peng在一系列特征上与牛姆瓜属Holboellia植物不同,不应隶属于该属,而代表了一个未被描述过的新属—长萼木通属。新属在茎、叶、果实和花的大部分特征上与木通属Akebia相似,但花萼特征又与野木瓜属Stauntonia接近,其系统位置介于这两个属之间,并偏于前者。     

A Preliminary Study on the Taxonomy of the Family Magnoliaceae

A new system of classification of Magnoliaceae proposed. This paper deals mainly with taxonomy and phytogeography of the family Magnoliaceae on the basis of external morphology, wood anatomy and palynology. Different authors have had different ideas about the delimitation of genera of this family, their controversy being carried on through more than one hundred years (Table I). Since I have been engaged in the work of the Flora Reipublicae Popularis Sinicae, I have accumulated a considerable amount of information and material and have investigated the living plants at their natural localities, which enable me to find out the evolutionary tendencies and primitive morphological characters of various genera of the family. According to the evolutionary tendencies of the characters and the geographical distribution of this family I propose a new system by dividing it into two subfamilies, Magnolioideae and Liriodendroideae Law (1979), two tribes, Magnolieae and Michelieae Law, four subtribes, Manglietiinae Law, Magnoliinae, Elmerrilliinae Law and Micheliinae, and fifteen genera (Fig. 1 ), a system which is different from those by J. D. Dandy (1964-1974) and the other authors. The recent distribution and possible survival centre of Magnoliaceae. The members of Magnoliaceae are distributed chiefly in temperate and tropical zones of the Northern Hemisphere, ——Southeast Asia and southeast North America, but a few genera and species also occur in the Malay Archipelago and Brazil of the Southern Hemisphere. Forty species of 4 genera occur in America, among which one genus (Dugendiodendron) is endemic to the continent, while about 200 species of 14 genera occur in Southeast Asia, of which 12 genera are endemic. In China there are about 110 species of 11 genera which mostly occur in Guangxi, Guangdong and Yunnan; 58 species and more than 9 genera occur in the mountainous districts of Yunnan. Moreover, one genus (Manglietiastrum Law, 1979) and 19 species are endemic to this region. The family in discussion is much limited to or interruptedly distributed in the mountainous regions of Guangxi, Guangdong and Yunnan. The regions are found to have a great abundance of species, and the members of the relatively primitive taxa are also much more there than in the other regions of the world. The major genera, Manglietia, Magnolia and Michelia, possess 160 out of a total of 240 species in the whole family. Talauma has 40 species, while the other eleven genera each contain only 2 to 7 species, even with one monotypic genus. These three major genera are sufficient for indicating the evolutionary tendency and geographical distribution of Magnoliaceae. It is worthwhile discussing their morphological characters and distributional patterns as follows: The members of Manglietia are all evergreen trees, with flowers terminal, anthers dehiscing introrsely, filaments very short and flat, ovules 4 or more per carpel. This is considered as the most primitive genus in subtribe Manglietiinae. Eighteen out of a total of 35 species of the genus are distributed in the western, southwest to southeast Yunnan. Very primitive species, such as Manglietia hookeri, M. insignis and M. megaphylla, M. grandis, also occur in this region. They are distributed from Yunnan eastwards to Zhejiang and Fujian through central China, south China, with only one species (Manglietia microtricha) of the genus westwards to Xizang. There are several species distributing southwards from northeast India to the Malay Archipelago (Fig. 7). The members of Magnolia are evergreen and deciduous trees or shrubs, with flowers terminal, anthers dehiscing introrsely or laterally, ovules 2 per carpel, stipule adnate to the petiole. The genus Magnolia is the most primitive in the subtribe Magnoliinae and is the largest genus of the family Magnoliaceae. Its deciduous species are distributed from Yunnan north-eastwards to Korea and Japan (Kurile N. 46’) through Central China, North China and westwards to Burma, the eastern Himalayas and northeast India. The evergreen species are distributed from northeast Yunnan (China) to the Malay Archipelago. In China there are 23 species, of which 15 seem to be very primitive, e.g. Magnolia henryi, M. delavayi, M. officinalis and M. rostrata, which occur in Guangxi, Guangdong and Yunnan. The members of Michelia are evergreen trees or shrubs, with flowers axillary, anthers dehiscing laterally or sublaterally, gynoecium stipitate, carpels numerous or few. Michelia is considered to be the most primitive in the subtribe Micheliinae, and is to the second largest genus of the family. About 23 out of a total of 50 species of this genus are very primitive, e.g. Michelia sphaerantha, M. lacei, M. champaca, and M. flavidiflora, which occur in Guangdong, Guangxi and Yunnan (the distributional center of the family under discussion) and extend eastwards to Taiwan of China, southern Japan through central China, southwards to the Malay Archipelago through Indo-China. westwards to Xizang of China, and south-westwards to India and Sri Lanka (Fig. 7). The members of Magnoliaceae are concentrated in Guangxi, Guangdong and Yunnan and radiate from there. The farther away from the centre, the less members we are able to find, but the more advanced they are in morphology. In this old geographical centre there are more primitive species, more endemics and more monotypic genera. Thus it is reasonable to assume that the region of Guangxi, Guangdong and Yunnan, China, is not only the centre of recent distribution, but also the chief survival centreof Magnoliaceae in the world.