云南猪屎豆属植物订正(续)——植物地理学讨论

本文根据猪屎豆属植物的外部形态和细胞染色体特征以及地理分布特点,论述了该属植物的起源、发展和迁移等问题;并运用组相似性和种相似性分析方法,论证了非洲、马达加斯加和印度之间,以及印度与其在亚洲的邻近地区之间在种类组成上的共有关系和亲缘关系。本文还侧重于该属植物在云南的分布格局,提出它们从印度向中国散布的可能存在路线。     

“田中线”及其在生物地理上的运用问题

日本学者根据对柑桔种系的地理分布设想了一条从云南西北部(28°N,98°E)向东南部延伸到越南北部东京湾(大约18°45’N或19°N、108°E)的分界线,将其命名为"柑桔分布的田中线",简称"田中线"。后来它被认为在区分中国-日本植物分布属与中国-喜马拉雅分布属上具有生物地理意义,并与一些兰科植物属的分布相结合提出了"田中-楷永线",建议将它作为一条划分东亚植物区系东部的中国-日本植物亚区与西部的中国-喜马拉雅植物亚区的区系线。一些研究显示该线对一些物种的种群分化和谱系地理有意义,但主要是气候和地貌引起的环境梯度变化,不支持它是一条古老的生物地理分界线。另外,这条"柑桔分布的田中线"本身,未得到柑桔属内及其近缘属的系统发育关系研究的支持。云南植物区系的生物地理分异明显,但与"田中线"无显著联系,在云南植物区系分区上,"田中线"也基本无意义。云南复杂的地质历史、多样的气候和地貌,影响了植物区系的生物地理分异,用这条设想的从云南西北部向东南部延伸的斜直线作为一条生物地理界线,与最近的研究具有不相符性。     

Phylogeography and molecular diversity analysis of Jatropha curcas L. and the dispersal route revealed by RAPD,AFLP and nrDNA-ITS analysis

Jatropha curcas L. (Euphorbiaceae) has acquired a great importance as a renewable source of energy with a number of environmental benefits. Very few attempts were made to understand the extent of genetic diversity and its distribution. This study was aimed to study the diversity and deduce the phylogeography of Jatropha curcas L. which is said to be the most primitive species of the genus Jatropha. Here we studied the intraspecific genetic diversity of the species distributed in different parts of the globe. The study also focused to understand the molecular diversity at reported probable center of origin (Mexico), and to reveal the dispersal route to other regions based on random amplified polymorphic DNA, amplified fragment length polymorphism and nrDNA-ITS sequences data. The overall genetic diversity of J. curcas found in the present study was narrow. The highest genetic diversity was observed in the germplasm collected from Mexico and supports the earlier hypothesis based on morphological data and natural distribution, it is the center for origin of the species. Least genetic diversity found in the Indian germplasm and clustering results revealed that the species was introduced simultaneously by two distinct germplasm and subsequently distributed in different parts of India. The present molecular data further revealed that J. curcas might have spread from the center of the origin to Cape Verde, than to Spain, Portuguese to other neighboring countries and simultaneously to Africa. The molecular evidence supports the Burkill et al. (A dictionary of the economic products of the Malay Peninsula, Governments of Malaysia and Singapore by the Ministry of Agriculture and Co-operatives. Kuala Lumpur, Malaysia, 1966) view of Portuguese might have introduced the species to India. The clustering pattern suggests that the distribution was interfered by human activity.     

A preliminary study on Sabiaceae of China

This paper is a preliminary study on the Sabiaceae in aspects of its morphology, taxonomy and geography. We propose that the Sabioideae and Meliosmoideae as two new subfamilies of Sabiaceae according to the external morphology, flower structure and geographical distribution of these two genera respectively. This paper follows the taxonomic concepts of Luetha Chen on Sabia and C. F. van Beusekom on Meliosma. We agree with them for their classification of these two genera above the specific rank. As to the revision work of Sabia by van de Water and C. F. van Beusekom’s work on Meliosma we disagree for their unduly broad specific concepts. We rather treat the species of these two genera according to their habitats in regions on a relatively narrower sense. The genus Sabia of China are classified into 2 tribes, with 16 species, 5 subspecies and 2 varieties in which 4 subspecies and l variety are as new combinations, the genus of Meliosma in China are classified into 2 subgenera with 29 species, and 7 varieties of which 4 varieties are new combinations. After examining the affinity of the species of Sabia and Meliosma in China and its neighboring nations such as Burma, Japan and Bhutan, we found that their migration initiated from China, as the primitive species of these two genera occured in northeast and central part of Yunnan, sou theast of Sichuan, north of Guizhou and west of Hubei, the region may probably be the main origin of these two genera. As shown in tables 1 & 2, the localities where the species of these two genera densely populate they are from Yunnan, Guangxi, and Guangdong coinciding with the concepts of C. F. van Beusekom and van de Water about the distribution of exotic species of these two genera, it may reasonable be pointed out that the center of distribution of these two genera is Yunnan, Guangxi, Guangdong and nieghboring nations, upper Burma and northern Vietnam. Futhermore, it may be seen that starting from this center the number of species become less and less as they proceed far and far awaybut become more advance in evolution.     

赖草属的地理分布及其起源散布

为了探讨赖草属（Leymus Hochst.）植物的地理分布及起源散布,通过野外调查、标本查阅和文献搜集,同时结合地史、气候及类群演化关系的综合分析,对其地理分布及起源散布进行了整理和研究。结果显示,赖草属植物有3组53种（含变种）,主要分布于欧亚大陆和北美地区;中国有3组40种（含变种）,主要分布于西北、华北、东北以及西南地区,也是该属种类最为集中的区域;尤其是新疆北部的阿尔泰地区及青藏高原东北部的唐古特地区又是中国该属分布相对密集之地,有3组22种,并且其间不同等级、不同系统演化水平的类群均有分布,是该属的现代分布中心。同时,阿尔泰地区多汇集赖草属不同等级的原始类群和外类群,故该地区极有可能是该属的起源地,起源时间大约在第三纪渐新世。赖草属起源后,在渐新世末期青藏高原不断隆升、气候与环境发生巨变,其在中国境内地质活动较为剧烈的区域得到进一步发展和分化,主要通过两个阶段和三条路径扩散成现今的地理分布格局。     

菅属植物的地理分布

菅属(Themeda Forssk.)是禾本科高粱族(Poaceae:Andropogoneae)中佛焰苞物种的代表类群之一,在高粱族占据关键的系统演化位置,具有高度的形态和生态多样性。通过野外调查和查阅标本及文献,菅属约有27种植物,旧世界均有分布,新世界3种隶属于菅组。中国有13种,分布在西南至华南各省(区),云南干热河谷地区有10种。研究表明中国云南及印度北部是菅属的分布中心和多样性中心,中国云南及印度北部是否为菅属的起源地尚需确证。     

中国兜兰属植物生态地理分布

分析了国产兜兰属植物的生态地理分布特点和发展趋势及兜兰属植物的系统演化趋势与生态地理环境的关系。国产兜兰野生种共有 18种 ,主要分布于热带过渡地区 (南亚热带 ) ,主产西南各省区 ;大多数种类生长于石灰岩山地 ,多为半附生兰 ,呈丛生生长 ,另一部分生长于酸性砂岩面的腐叶土上 ,多为地生兰 ,呈单株生长或分蘖状散生 ;大部分兜兰分布于较高海拔地区 ;国产兜兰属中最原始的短瓣亚属绝大部分种类仅分布在滇东南地区与贵州、广西连成一片的岩溶地貌的石灰岩地区 ,而兜兰属中较进化的兜兰亚属大部分种类在本区皆有分布。以上说明滇东南的石灰岩地区可能是兜兰属的起源中心和演化中心 ,中国的南亚热带地区是兜兰属植物的生态多样性中心     

The Evolution and Distribution of Subfam. Spiraeoideae (Rosaceae) of China,with Special Reference to Distribution of the Subfamily in the World

The subfam. Spiraeoideae, consisting of 22 genera and more than 260 species in the world,is the most primitive subfamily of Rosaceae. It has developed into two groups,i.e. evergreen and deciduous ones, of which eight genera and 100 species in China are totally deciduous. In the present paper, the origin,evolution and distribution of the Chinese genera is discussed mainly, and the distribution of the whole subfamily in the floristic regions of the world is also mentioned. Based on evolutionary trends of morphological characters, Spiraea L. is considered as the most primitive genus in the deciduous group of subfam. Spiraeoideae, from which some genera are been derived, the systematic position and evolutionary relationships between different genera are elucidated in this paper. Through the analysis on the geographical distribution of the genera in China, the areal types may be divided as follows: (1) North Temperate Type: Spiraea, Physocarpus, Aruncus. (2) East Asian and North American Disjunct Type: Sorbaria. (3) Mediterranean, West Asian (or Central Asia) and East Asian Type: Sibiraea. (4) Temperate Asian Type: Exochorda.(5) East Asian Type: (a) Sino Himalayan Distribution: Neillia; (b) Sino Japan Distribution: Stephanandra. After analysis of the distribution of subfam. Spiraeoideae in the world, it is shown that the Eastern Asiatic Region, being the richest in genera, species and endemic species of the world,is not only the center of distribution and differentiation,but also an important region for occurrence and development of some deciduous genera of this subfamily, while in North America, the Madrean Region and Rocky Mountain Region, genera, species and endemic species are abundant, which indicates that the western part of North America is also the distribution center of this subfamily at the present, but it may be the secondary center of distribution. It can be seen that the relatively primitive and evergreen g enera, i.e. Quillaja and Kageneckia, are now confined to South America. The fact implies that the South America may be the region for early differentiation and development of the evergreen genera in Subfam. Spiraeoideae. The analysis of Chinese plants has shown that China has the most members of the subfamily in Eastern Asiatic Region, with eight genera, 82 species and 62 endemic species and that the maximum concentration is in western Sichuan, northwestern Yunnan and their adjacent areas. It is very obvious that the center of distribution and diversity of Subfam. Spiraeoideae in China lies in the Hengduan Mountain Region of Sino Himalayan Forest Subkingdom and the western part of Sino Japan Forest Subkingdom, where may be the birthplace of some genera in China. It may be considered that the deciduous genera of Subfam. Spiraeoideae might have originated in Laurasia.According to the fossil records, the time of origin of Subfam.Spiraeoideae dates back to the Lower Cretaceous.     

云南水龙骨科星蕨亚科植物的区系地理研究

对云南水龙骨科星蕨亚科植物种类的地理成分进行了划分,并对云南与邻近地区的区系联系进行了比较,对云南该亚科植物的区系起源也作了探讨。得出如下结论云南是中国水龙骨科星蕨亚科植物的现代地理分布中心;该亚科植物是典型的热带亚洲的区系成分;与广西和越南北部的区系联系最密切;云南东南部和越南北部是水龙骨科星蕨亚科植物的多样性中心。     

云贵高原及横断山区莲座蕨科植物地理分布

依据云南大学植物标本馆蕨类植物标本室(PYU)和国内主要标本馆保存的莲座蕨科植物标本,以及多年来积累的研究资料,建立该科植物在云南的产地GIS数据库。以此为基础,分析云南莲座蕨科植物空间分布的多样性和特有性,及其在云贵高原及横断山区的地理分布特征。研究结果如下：① 云南莲座蕨科植物种类丰富,分布海拔范围为100~2400m;② 滇东南是莲座蕨科植物分布的多样性和特有性中心,其多样性由滇东南向西、北方向递减;③ 云南有莲座蕨科2个属分布,即莲座蕨属(Angiopteris)和原始莲座蕨属(Archangiopteris),其中原始莲座蕨属的物种多样性较低而特有性较高。初步分析了该科植物中5个广布种和1个高山峡谷种分布格局的成因,以及5个特有种的发生史,推断广布种的分布格局形成于第四纪冰期之前,高山峡谷种的分布格局形成于第三纪之后,而特有种的主要成因可能是自然杂交和边缘效应。     

中国蔷薇科绣线菊亚科的演化、分布——兼述世界绣线菊亚科植物的分布

绣线菊亚科是蔷薇科最原始的亚科,共有22属260余种, 包括常绿和落叶两大类群,前者是 原始类型。我国有8属100种,全都为落叶性。本文着重讨论中国各属的起源、演化和分布等 ,同时也概述全亚科植物在世界各植物区的分布等问题。绣线菊属Spiraea是该亚科落叶类群中最原始的属,它在早期发生趋异进化,衍生出形态各异而亲缘关系密切 的不同属,本文阐明了中国各属的系统位置和属间的亲缘关系。通过对我国各属地理分布的 分析对比,属的分布区可归纳为5个类型。对全球绣线菊亚科植物在世界各植物区中的属、种数统计表明,东亚区有8属105种,其中有96个特有种,是该亚科植物分布最多而又最集中 地区,具有在系统发育上处于各主要演化阶段的落叶类型,因此,东亚区是全球绣线菊亚科植 物的现代分布和分化中心,也是落叶类群发生和发展的关键地区。在北美洲,从马德雷区至落基山区一带分布着11属46种,均为特有种,显然北美洲西部也是该亚科植物的现代分布中心,但可能是第二分布中心。南美洲至今保存2个较古老的常绿属,即Quillaja和K ageneckia,基于此,南美洲可能是绣线菊亚科某些常绿属早期分化和发展的关键地区 。中国绣线菊亚科植物在东亚区占绝对优势,有8属82种,其中有62个特有种,分别占该区属 、种和 特有种数的100%、82%、和65%, 这些类群分布最密集地区是在中国喜马拉雅森林植物亚区 中的横断山脉地区和中国日本森林植物亚区的西部,这一带是中国绣线菊亚科的现代分布和多样性中心,很可能是某些属的发源地。由此看来,绣线菊亚科的落叶属可能起源于劳亚古陆。据化石记载,该亚科植物的起源时间可以追溯到白垩纪早白垩世。     

The Origin,Dispersal and Formation of the Distribution Pattern of Swertia L. (Gentianaceae)

The genus Swertia is one of the large genera in Gentianaceae, including 154 species, 16 series and 11 sections. It is disjunctly distributed in Europe, Asia, Africa and N. America, but entirely absent from Oceania and S. America. According to Takhtajan’s (1978) regionalization of the world flora, Swertia is found in 14 regions. Eastern Asiatic region with 86 species, of which 58 are local endemics, 13 series and 9 sections, ranks the first among all the regions. The highest concentration of the taxa and endemics in Eastern Asiatic region occurs in SW China-Himalayan area (Sikang-Yunnan P. , W. Sichuan, W. Yunnan-Guichou Plateau of China and NE. Burma, N. Burmense P. , E. Himalayan P. and Khasi-Manipur P. ). In this area there are 74 species (48 endemics), 12 series, and 9 sections; thus about half species of the world total, three quarters of series and 82% of sections occur in this small area. Besides, the taxa at different evolutionary stages in Swertia also survive here. It is an indication that SW. China-Himalayan area is a major distribution centre of the genus Swertia. In addition, Sudan-Zambezian Region in Africa, with 22 species, 4 series and 2 sections, is a second distribution centre. The primitive type of the genus Swertia is Sect. Rugosa which consists of 2 series and 23 species. It is highly centred in the mountains of SW. China (Yunnan, Sichuan, Guizhou and SE. Xizang) where 2 series and 16 species occur. Among them 15 species of Ser. Rugosae were considered as the most primitive groups in this genus. From our study, the outgroup of Swertia is the genus Latouchea Frahch. , which is distributed in Yunnan, Sichuan, Guizhou, Hunan, Guangdong, Guangxi and Fujian. The two groups overlap in distribution in SW. China. According to the principle of common origin, the ancestor of two genera ap peared most probably in this overlapping area. It was inferred that SW. China Was the birth-place of the genus Swertia. Four sections of Swertia have different disjunct distribution patterns: Sect. Ophelia is of Tropic Asia, Africa and Madagascar disjunct distribution; sect. Swertia is of north temperate distribution; sect. Spinosisemina is in Tropical Asia (Trop. India to S. China and Philipines); sect. Platynema also is in Tropical Asia (Java, Sumatra, Himalayas to SW. China). These disjunct patterns indicate that the Swertia floras between the continents or between continent and islands have a connection with each other. From paleogeographical analysis, Swertia plants dispersed to Madagascar before the Late Cretaceous, to SE. Asian Islands in the Pleistocene, to North America in the Miocene. The distribution of Swertia in Madagascar might be later than that in Asia. Therefore the origin time of the genus Swertia was at least not later than the Late Cretaceous, and might be back to the Mid-Cretaceous. The genus Swertia first fully developed and differentiated, forming some taxa at different evolutionary stages (Rugosa, Swertia, Poephila, Ophelia and Platynema etc. ) in the original area, and these taxa quickly dispersed in certain directions during the Late Cretaceous-Middle Tertiary when the global climate was warm and no much change. There seem to be three main dispersal routes from the origin area to different continents; (1) The westward route i. e. from SW. China, along the Himalayas area to Kashmir, Pakistan, Afghanistan and Iran, and then southwestwards into Africa throuth Arabia. Four sections (Poephila, Macranthos, Kingdon-Wardia and Ophelia) took this dispersal route. Most species of sect. Ophelia dispersed along this route, but a few along southern route and north ern route. Sect. Ophelia greatly differentiated in Africa and the African endemic sectionSect. Montana was derived from it. The two sections form there a second distribution center of Swertia. (2) The southward route, i. e. towards S. India through the Himalayas, and towards SE. Asian islands through C. and S. China, Indo-China. Along this dispersal route sect. Platynema, Sect. Spinosisemina and a few species of Sect. Ophelia dispersed; (3) The northward rout, i. e. northwards across N. China, C. Asia to a high latitude of Euasia, and also through E. Asia into N. America. The following groups took this route: sect. Rugosa, sect. Swertia, sect. Frasera, sect. Heteranthos and sect. Ophelia ser. Dichotomae. Therefore, it seems that the genus Swertia originated in SW. China and then dispersed from there to N. and S. Asia, Africa, Europe and North America and formed the moderndistribution pattern of this genus.     

西双版纳热带雨林蚂蚁区系的起源与演化

从早寒武纪至早侏罗纪,西双版纳古陆一直与其南面的缅甸古陆连为一体,并具有相同的物种起源和演化历史,但西双版纳古陆分别于晚石炭纪和中,晚侏罗纪两次沦为海洋,其物种起源与演化成果前功尽弃,蚂蚁起源于白垩纪中后期或更早,大量分化于第三纪,至白垩纪早期,西双版纳古陆同时与南面的缅甸古陆和北面的中国古陆 为一体,从此再未沦陷,因此西双版纳的物种是此时开始从缅甸古陆和中国古陆同时移入的,至第三纪喜马拉雅造山运     

柚的起源、演化及分布初探

柚 (Ｃｉｔｒｕｓｇｒａｎｄｉｓ (Ｌ .)Ｏｓｂｅｃｋ)是桔属的三个基本种之一 ,是一类重要的种质资源 ,经济价值高 ,近年来国内外的开发利用方兴未艾。柚果以其果形美观 ,味道鲜美 ,营养丰富 ,且耐储藏 ,易运输 ,素有“天然罐头”之称。我国是柑桔的起源中心和遗传变异中心之一 ,资源极其丰富。中国柚的人工栽培最早 ,夏书《禹贡》就有“扬州厥包橘柚锡贡”的记载 ;《吕氏春秋》有“果之美者 ,云梦之柚”之说 ,证明柚的栽培至少有三千多年的历史。我国目前在广东、广西、福建、四川、台湾、湖南、江西、浙江、江苏、安徽、云南、贵州、湖北…     

木兰属(Magnolia)的地理分布及起源

分析了现代木兰属（Ｍａｇｎｏｌｉａ）植物的地理分布及其散布途径,认为华夏植物区系区域不仅是现代木兰属的分布中心,同时也是木兰属的分化中心及原始类群保存中心,并结合地史资料,推断全球木兰属植物应共同起源于华夏植物区系。     

云南德宏傣族景颇族自治州竹亚科(禾本科)植物区系地理研究

云南南部和西南部是中国竹类资源最为丰富的地区 ,与其邻近地区一起构成了世界木本竹类的多样性中心。德宏正处于这个中心位置 ,竹子种类丰富 ,有 16属 5 6种及变种 ,其中中国特有种 2 1种 (云南特有 15种 ) ,占其竹亚科全部区系成分 (45种 )的 4 6 6 7%。热带亚洲分布类型占绝对优势 ,本地区的竹亚科区系与热带亚洲特别是缅甸 (有 18种共有种 )及云南南部和东南部有非常密切的联系     

云南省古茶树资源调查与分析

为更好地保护和开发利用古茶树资源,2010-2017年对云南省12个地区58个县/市的古茶树资源进行了全面普查,依据《Flora of China》英文修订版分类确立了古茶树资源物种名录,建立初步的古茶树资源数据信息库。以此为基础,利用地理信息系统和统计学分析了云南古茶树资源种类组成、地理分布特征、生境类型及形态多样性。结果表明:云南古茶树种类多,调查共获得古茶树资源分布点474个,记录样本植株2570份,隶属7种6变种;古茶树资源分布广而不均,主要分布于滇西、滇南、滇东南及滇中哀牢山山脉,滇东南是古茶树物种多样性的分布中心,滇西是特有种的分化中心,云南古茶树资源的地理分布可能存在滇西-大理茶(Camellia taliensis(W.W.Sm.)Melch.)、滇南-普洱茶(C.sinensis var.assamica(J.W.Mast.)Kitam.)和滇东南-厚轴茶(C.crassicolumna H.T.Chang)3个现有分布中心;古茶树资源生境复杂多样,可大致分为原生林、次生林和高山旱地等3类,不同生境分布的古茶树种类及其生长状况有差异;古茶树资源具有丰富的形态多样性,其描述型性状多样性指数为0.58~1.48,数值型性状变异系数为4.37%~51.03%,总体上营养器官的变异性高于花部器官。本工作为进一步探讨云南地区古茶树资源的系统演化、多样性保护及合理利用提供了重要的本底资料。此外,根据古茶树资源现状,初步提出了一些保护利用建议。     

云南毛翅目昆虫区系研究

云南已知毛翅目昆虫２４科７７属３２１种,含云南特有种１５２种。其中东洋界分布成分占８３％,东洋－古北界东部共布成分占９％,东洋－古北界西部共布、东洋－非洲界共布和广布成分所占比例均小于４％。云南毛翅目在我国的分布以西南型（４４％）、华南型（２１％）和西南－华南共布型（９％）为主,其次为向东扩散的西南－华南－华中（５％）和华南－华中（４％）共布型。云南与毗邻省四川的毛翅目区系关系最密切,其次是西藏和     

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。     

Biodiversity of Bitahai Nature Reserve in Yunnan Province, China

Bitahai Nature Reserve is located in Northwest Yunnan and is the highest elevation and the highest latitude wetland nature reserve in Yunnan Province. Bitahai Nature Reserve is a typical wetland nature reserve in very low latitude and high elevation with large areas of coniferous forest around the alpine till lakes, wetland and water area ecosystem while compared with natural reserves distributed same latitude in the world. The area of the reserve distribution is the key area of Transverse Mountain Region. It was a refuge for plant and wildlife because Transverse Mountains were not covered by ice in the Tertiary. And the area is now regarded as a center of forming new species and preserving ancient species. Species biodiversity is high and the distribution of some endemic animals and plants are limited in Transverse Mountains area. In the nature reserve, there are many first and second grade protected plants and animals listed in Lists of China National Priority Protection Fauna and Flora. All of these are precious materials of genetic diversity. The diversities of the plant community and vegetation contribute to ecosystem diversity. Thus, Bitahai Nature Reserve holds with high conservation value. However, its biodiversity is threatened by different factors and its conservation should be paid great attention.