云南西双版纳兰科植物

云南西双版式纳是我国兰科植物分布最集中的地区之一,经多年的野外考察和采集整理后,迄今计有96属335种和2个变种,有2个属为全国新记录,190种为西双版纳的新记录,其中50个种是全国新记录,21种为本区特有种,该地区的兰科种属类群远超过海南省而相当于台湾省。     

广西植物的新记录

报道了近年发现的广西新记录植物 2 1种 ,同时还对广西金秀县特有种大齿马铃苣苔的形态特征做了补充记述。这些新记录植物的绝大多数种类系采自广西猫儿山自然保护区 ,是猫儿山植物区系的重要组成部分。     

福建省悬钩子属植物资源的调查、收集、评价和利用的研究

本文对福省建悬钩子属植物的种类和分布进行了调查研究,该属植物在福建计有41种,5变种。其中1种、1变种是新分布。     

广西禾本科植物二新记录属

该文报道了广西禾本科(Poaceae)植物二新记录属,即菵草属( Beckmannia Host)和草沙蚕属( Tripogon Roem. et Schult.)。菵草属有2种及1变种,分布较广,我国有1种1变种,广西首次记录到该属的菵草[ Beckmannia syzigachne (Steud.) Fern.]。草沙蚕属约有30种,多分布于亚洲和非洲,我国有11种,广西首次记录到该属的线形草沙蚕( Tripogon filiformis Nees ex Steud.)。同时,还提供了2个新记录属、种的形态描述与照片。     

广西弄岗国家级自然保护区植物物种多样性初步研究

对广西弄岗国家级自然保护区(以下简称弄岗保护区)维管植物物种多样性组成,包括对异名的订正、新发现类群和新发表类群的添加以及广西新记录种、特有种、国家或区级重点保护物种的统计等进行整理和研究。结果表明:弄岗保护区共计有维管植物1752种,隶属于184科810属。其中蕨类植物中国特有种39种、种子植物广西特有种101种、岩溶特有植物278种、珍稀濒危植物33种、广西重点保护野生植物73种、广西新记录种9种以及植物新类群17种。     

广西大戟科植物资料

<正> 广西的大戟科植物种类众多。作者对广西中草药原植物研究过程,将已采集的标本及华南植物所标本室(SCBI)和广东、广西主要标本室(均有注明)收藏的广西及其邻近地区的大戟科标本进行整理;现报道(一)、三宝木属植物摘记;有5种和3个新变种,其中广西产5种、1变种。(二)、广西白大凤属植物;1种。     

中国黑龙江省异极藻科植物研究

报道了采自中国黑龙江省（包括吉林、内蒙古的部分地区）的异极藻科植物３属２５种２４变种６变型。其中２种７变种３变型为中国新记录。我们初步探讨了黑龙江省异极藻科植物的分布特征并对这些新记录进行了描述和讨论,此外还附有全部分类单位的照片及其生境和分布一览表。     

子午岭种子植物区系分析

子午岭林区计有种子植物94科361属689种。其中裸子植物3科8属10种1变种;被子植物91科353属678种。中国特有属8个,特有种271个,子午岭特有种1个。其种子植物区系的基本特征是：植物种类相对丰富;区系成分复杂,多种成分交汇;区系组成以华北成分为主体,以温带成分占优势;南北区系成分存在差异,垂直分布带谱不明显;在中国植物区系上隶属于泛北极植物区中国-日本森林植物亚区的华北地区黄土高原植物亚地区。     

甘肃省杓兰属植物资源调查及2新记录种

通过对甘肃省杓兰属植物进行系统的调查和资料整理,共发现甘肃省杓兰属植物15种,占中国杓兰属植物种类的39.47%,其中9种为中国特有种。调查发现2种甘肃省杓兰属植物分布新记录种——巴郎山杓兰(Cypripedium palangshanense T.Tang et F.T.Wang)和离萼杓兰(Cypripedium plectrochilum Franch.)。通过整理重新编制了甘肃省杓兰属植物的分种检索表。     

中国淡水双壳类特有种的地理分布

通过查阅有关文献整理得出,中国淡水双壳类特有种计有58种,隶属于双壳纲(Bivalvia)2科17属,其中主要是蚌科(Unionidae)的种类(16属57种)。我国淡水双壳类特有种的组成和区系成分,以东洋界华中区的种类占绝对优势,仅有少数种类渗透到古北界;特有种在我国16个省有分布,但主要集中分布于江西、湖南、安徽、浙江、江苏五省。双壳类特有种的形成和保存可能与我国古地理环境及其生活的水域环境有关。     

广西玄参科简志及其地理分布特点

在广西植物区系中,玄参科属于中等大小的科,计３１属９６种（变种）（另有栽培部分８属１３种已除外）．广布于全区各地．作者近年编《广西植物志》（玄参科）时．全面整理研究了该科广西的馆藏标本。现将其中科研或经济价值较大的部分分类群含广西新记录的３属１９种）加以简报,以资利用。同时,对本科在广西的地理分布特点亦作一初探。     

广西特有植物区系特征研究

分析论述了广西特有植物区系特征。结果表明:(1)广西特有植物共859种,隶属于119科303属,其中蕨类植物15科22属42种,裸子植物3科4属7种,被子植物101科277属810种。这些特有种中,以草本植物种类最多,有440种,灌木、乔木类型次之。(2)地理成分复杂多样,分布交错混杂。种子植物科包含9个分布类型,属包含14个分布类型。种则依据在广西区内地理分布可划分为5个分布亚型,其中以桂西南分布种类最多。(3)科属种的水平上都表现出明显的的热带-亚热带性质。4.区系成份兼具古老性和年青性,并表现出岩溶地区特有化发展的特征。     

山东昆嵛山植物区系初步研究

昆嵛山地处胶东半岛,属于暖温带气候类型;植物种类丰富,有维管植物132科,571属,1058种。地理成分复杂,区系类型多样,现有571个属可分为15个分布型及12个变型。区系组成的大科及主要科共16科,即菊科,禾本科,豆科,蔷薇科,莎草科,百合科,十字花科,蓼科等,共有植物285属,612种,占昆嵛山种子植物总属数的51.82%,总种数的59.94%,它们构成了昆嵛山植物区系的基本框架。Raunkiaer生活型组成依次为高位芽植物(34.40%)> 地面芽植物(27.13%)> 一年生植物(19.66%)> 隐芽植物(9.64%)> 地上芽植物(9.17%)。本文在主要区系地理成分分析的基础上,得出本区系植物具有以下4个特点:(1)植物种类丰富,温带成分优势明显,热带成分比例较大(2)分布类型多样,地理成分复杂,显示出多方植物交汇的特点(3)区系成分具有一定的古老性,单种属成分较多,区系的特有程度较低(4)珍稀濒危种类丰富,在科的层次上较为集中。     

广西野生阴生观赏植物资源及其特点

为了解广西境内蕴藏的野生阴生观赏植物资源及珍贵种质,采取野外实地考察及标本采集鉴定相结合的方法,对广西全境分布的阴生和半阴生观赏植物资源进行研究。结果表明:广西野生阴生观赏植物有5个基本特点:种类丰富(162科485属1309种)、种质资源珍贵(珍稀植物195种,广西特有植物136种)、生长基质多样(喜钙植物、喜酸植物和中间类型植物)、草本性状比值显著(草本植物约占总种数的66.1%)、野生资源贮藏量的多寡悬殊性。6个主要野生阴生观赏类群为:蕨类植物(43科240种)、兰科(37属126种)、百合科(21属82种)、苦苣苔科(17属63种)、秋海棠科(1属43种)、天南星科(12属30种)。研究结果可为合理开发利用广西野生阴生观赏植物资源提供参考。     

江苏野生藤本植物多样性初探

通过野外调查和文献资料查阅,初步统计出江苏野生藤本植物共有35科74属153种,其中蕨类植物有1科1属1种,单子叶植物有3科4属12种,双子叶植物有31科69属140种。该区藤本植物以寡种科(属)、单种科(属)为主;地理成分复杂,具有明显的热带亲缘性,并受温带成分的影响。生长型以木质藤本为主(56.58%),草质藤本次之,其中,共有17科全为木质藤本,如木通科(Lardizabalaceae)以及防己科(Menispermaceae);共有13科全为草质藤本,如百部科(Stemonaceae)以及萝藦科(Asclepiadaceae)等;共有4科含木质与草质藤本植物,如百合科(Liliaceae)以及葡萄科(Vitaceae)等。高位芽植物最多(56.58%),地面芽植物(20.39%)、一年生植物(11.19%)、地下芽植物(8.55%)及地上芽植物(3.29%)的数量依次减少。该区藤本植物攀援类型可以分为4大类,以缠绕类居多(40.13%),其他依次是卷曲类(30.26%)、搭靠类(22.37%)以及吸固类(7.24%)。有性繁育系统以两性花最多(76.97%),单性花次之(19.74%),杂性花最少(3.29%);花序组成丰富,以无限花序占有绝对优势(71.05%)。     

中国杜鹃花科的(纟戾)木亚科白珠树亚科北极果亚科地理分布及其与其他地区的关系

<正> 杜鹃花科(Ericaceae)为中国植物的第七大科。因此,它在中国植物地理是中国植物区系上都占有比较重要的地位。杜鹃花科共分五个亚科:杜鹃花亚科、綟木亚科,白珠树亚科、北极果亚科和乌饭树亚科。綟木亚科、白珠树亚科和北极果亚科,虽然在本科中其种类不算太多,但所含10个属,故其多样性在本科中是首屈一指的。无疑,对这三个亚科在中国的地理分布及其与其他地区的关系的讨论是有意义的。     

Contributions to the pollen morphology and taxonomy of the Liliaceae

Pollen of 34 species from 7 genera of the Liliaceae were examined by LM and SEM with respect to the taxonomy of the family. Detailed pollen­morphological characteristics are given for all genera in the family on the basis of the results presented here together with data from the literature. The genera Tulipa and Lilium are heterogeneous in both aperture type and exine ornamentation. Pollen of Tulipa is monosulcate, 3-aperturate or inaperturate, with a microreticulate-striate, reticulate-implecto-striate, scabrate, perforate-rugulate, perforate-striate exine surface. Pollen of Lilium is monosulcate and 3-porate with a macroreticulate exine. The other genera are homogeneous in possessing of single longitudinal aperture (type monosulcate). The pattern of exine ornamentation and the structure of the aperture and its membrane are peculiar features for species and genera. Pollen of Erythronium and Tulipa are occasionally operculate, while in other representatives of the Liliaceae an operculum is lacking. Pollen morphological data support the division of the family into 3 tribes, namely Lloydieae, Lilieae, and Tulipeae.     

广西五皇山地区植物区系特性

为揭示广西南部五皇山地区的植物区系特征，通过野外调查和文献查阅，对广西五皇山国家地质公园及邻近区域的植物资源进行调查研究。结果表明，五皇山地区分布野生植物1 002种，隶属于167科581属，包括蕨类植物20科37属73种, 裸子植物3科4属5种，被子植物144科540属924种，以被子植物占优势。科属的地理成分均以热带成分为主，属的热带性更强，其中泛热带成分占最大优势，温带成分则以北温带为主。中国特有属4属，未见中国特有科。该地区植物区系总体表现为物种丰富度高，区系热带性质强，特有性弱的特征。     

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.