壳斗科的地质历史及其系统学和植物地理学意义

在收集整理现有壳斗科化石资料的基础上,讨论了壳斗科及其各属的起源时间、地史分布和地史 演替过程以及这些化石资料在系统学和植物地理学上的意义。白垩纪尚无壳斗科可靠的大化石记录, 微化石需要进一步研究才能确定亲缘关系以及古新世壳斗科已经分化出两个类群。从以上这些事实推 论壳斗科起源于白垩纪晚期,而壳斗科现代各属出现的时间应不晚于古新世。最早发现的壳斗科化石和现代栗亚科和水青冈亚科在形态结构上非常相似,这一事实表明,壳斗科分为两个亚科的观点更接近客观事实。在水青冈亚科中,三棱栎类的化石最早出现;在栎属中,青冈亚属更接近祖先类群;在地史中全缘栎类较具齿栎类出现早,粗齿的落叶栎类出现最晚。三棱栎属、栲属和石栎属的化石在老第三纪出现于北美和欧洲的事实说明,北美、欧洲和东亚在老第三纪时有一个相通的壳斗科植物区系。南美的三棱栎是通过北美进入南美的。中国横断山、欧洲地中海沿岸和北美西北部有一类形态特征相似、亲缘关系相近的硬叶栎类,它们之间有相同的地质演替历史,它们现代分布边界可能就是古地中海的边界。美洲的栎类有两个来源,常绿硬叶栎类是通过古地中海沿岸而经北美-欧洲陆桥到达的,落叶栎类则是在中新世以后通过白令海峡到达的。     

喜马拉雅东部雅鲁藏布江大峡弯河谷地区植被组成特点

论述了喜马拉雅东部雅鲁藏布江大峡弯河谷地区（即海拔６００～２５００ｍ）的植被组成特征。本地区原始植被主要有：（１）热带低山半常绿雨林,阿丁枫＋千果榄仁群落,阿丁枫＋小果紫薇群落,阿丁枫群落;（２）亚热带常绿阔叶林,刺栲＋阿丁枫群落,刺栲群落,短刺栲＋毛曼青冈＋西藏石栎群落,西藏栎＋毛曼青冈群落,通麦栎群落;（３）亚热带山地半常绿阔叶林,薄片青冈群落,俅江栎群落;（４）常绿针叶林,不丹松群落,喀西松     

云南宜良上新世栎属植物研究及其古环境指示意义

栎属(Quercus)植物叶片化石在新生代地层中分布普遍, 对亚热带常绿阔叶林具有重要的指示意义。本文对采自云南省宜良县上新统茨营组中的栎属植物叶片化石进行角质层结构分析, 结合叶形态特征, 系统描述了4种栎属植物: 阔叶栎(Quercus latifolia)、线叶栎(Q. scottii)、楔基栎(Q. simulata)和黄毛青冈相似种(Q. cf. delavayi)。通过对比化石和现生植物的叶形态和角质层特征, 本文认为叶片形状、叶基和叶尖特征、二级脉数量、表皮细胞和垂周壁特征、气孔大小和形状、气孔密度、毛基类型、形态和分布情况可以作为区分不同种类的特征, 但是不能只考虑其中的一个因素, 应该综合这些特征作为判断依据。结合宜良植物群中其他化石资料认为, 包括壳斗科柯属(Lithocarpus)、栲属(Castanopsis)以及樟科、榆科、木兰科等在内的植物, 代表了以栎属青冈组为优势树种的半湿润常绿阔叶林。宜良植物群与同时期相近纬度的植物群相比, 植被类型相似, 但是落叶成分较少。宜良植物群中的线叶栎、楔基栎和阔叶栎同晚始新世的线叶栎以及早中新世的楔基栎和阔叶栎相比, 形态并未发生大的变化, 与现生植物也非常相似, 进一步说明云南现代常绿阔叶林的主要成分来自于古老植物的承袭, 没有发生较大的改变。     

栲属(壳斗科)植物的现代和地史分布

根据文献资料和标本馆及化石记录,讨论了壳斗科栲属植物的现代分布和地史分布。现代栲属植物有110～134种,主要分布在东亚及东南亚,其中印度支那地区有82种栲属植物,是世界栲属植物分布最集中的地区,马来西亚地区是栲属特有种最丰富的事实是支持马来西亚地区与其它地区的区系交流十分有限的论据。中国栲属植物最丰富的地区是滇黔桂地区（29种）。栲属植物现代多样化中心在马来西亚和中南半岛。排除Chrysolepis后,栲属的分布类型应属热带亚洲分布。栲属在地质历史上有着比现在广泛的分布,最早、最可靠的栲属化石记录发现于北美始新世地层,欧洲和日本始新世也有栲属的化石记录,化石记录表明栲属起源的时间不晚于古新世,所有的壳斗科及栲属的化石都发现于北半球,现代分布也主要在北半球,壳斗科及栲属起源于北半球可以确认,由于化石证据与现代植物学的研究结果有较大差异以及关键地区化石证据的不足,具体的起源地尚不能肯定。     

云南的硬叶常绿阔叶林——古地中海残余植被

云南从干热河谷到寒温性山地广泛分布有一类常绿、阔叶、以壳斗科栎属植物为乔木优势种的森林植被，由于其独特的生态特征显示了与现代地中海地区硬叶栎林的相似性，而在群落的外貌、结构、特征种、地理分布等方面却与云南的亚热带常绿阔叶林有明显区别，因此被称为“硬叶常绿阔叶林”,它是在喜马拉雅隆升中因适应新的环境而发育的一个特殊植被类型。该植被的优势树种具有古地中海地区渊源，但在分布上大多为我国西南地区的特有种。硬叶常绿阔叶林除优势树种为硬叶栎类以外，其他种类与同域天然植被的物种组成基本一样，并没有一个独特的植物区系。硬叶常绿阔叶林群落结构简单，典型的硬叶常绿阔叶林群落有清楚的乔木、灌木和草本3个层次，而在生活型上，寒温性山地的群落以地面芽植物占绝对优势，干热河谷的群落以草本植物占优势。在中新世以前，硬叶栎类植物出现在湿润的热带-亚热带性质的古地中海常绿阔叶林里，直到上新世以后，现代的地中海式气候形成，适应干旱的地中海植物区系出现，并随喜马拉雅隆升，硬叶常绿阔叶林才从原先的热带-亚热带常绿阔叶林演化产生。     

壳斗科原始植物轮叶三棱栎在云南西双版纳的发现及其生物地理意义

于云南西双版纳发现了壳斗科植物的原始类群——轮叶三棱栎（Trigonobalanus verticillata Forman）。轮叶三棱栎被认为是栎属（Quercus L.）和水青冈属（Fagus L.）植物的祖先之一,原纪录分布于印度尼西亚和马来西亚,后来在我国海南岛被发现,其分布格局的形成一直未能合理解释。本次在云南新发现轮叶三棱栎,不仅可以解释它在海南岛的分布,也为海南岛历史上可能曾经连接着越南北部和广西西南部的假设提供了科学支持,具有重要的科研价值和生物地理学意义。     

槲栎叶复合群及其地史学和系统学意义

根据槲栎叶复合群研究的最新成果订正了国产槲叶栎属 (Dryophyllum)的化石。通过对该属 9种化石的整理 ,将 Dryophyllum dewalquei、D.parvum、D.relongtanense、D.yunnanensis和 D.sp.等 5种分别归入 Berryophyllum dewalquei、B.parvum、B.relongtanense、B.yunnanensis和 B.sp.;将 D.fushunense归入 Castaneophyllum fushunense;将 D.nervosaum归入 Quercusnervosum;将 D.relongtanense的一部分归入Q.lantenoisii;D.subfalcatum尚不能确定归属 ,但可以肯定不属槲栎叶复合群。同时 ,还讨论了槲栎叶复合群的地史学意义。该复合群是原始壳斗科向现代壳斗科过渡的中间类群 ,壳斗科各现代属出现的时间不早于古新世     

高山栎叶的形态结构及其与生态环境的关系

 对分布在不同生态环境条件下的硬叶常绿阔叶林建群种高山栎组植物叶的形态解剖特征进行了比较研究。结果表明,高山栎组植物叶的形态结构兼有非肉质旱生植物和高山植物的性状,这是它们对生态环境广泛适应的基础。每一个种除气孔器类型及腹面二层表皮细胞性状比较稳定外,其他性状,如气孔的大小和密度、表皮细胞的形状、垂周壁的类型、叶片的厚度、角质膜的厚度均受环境条件修饰,不是稳定性状,不具分类学意义。对同一个种的不同生活型,如乔木、小乔木和灌木,在解剖结构土没有明显的区别特征。地中海的冬青栎(Quercusilex)的表皮特征和高山栎组植物有很大的相似性。     

喀斯特退化天坑阴坡阳坡壳斗科植物的功能性状特征

喀斯特退化天坑的负地形生境中阴坡和阳坡的局域环境具有显著差异,导致植物群落类型差异明显。本研究以云南沾益退化天坑深陷塘为例,探究退化天坑阴坡与阳坡壳斗科植物功能性状特征,有助于揭示天坑的物种多样性保护库价值。结果表明: 阴坡土壤营养物质含量高于阳坡,阴坡壳斗科植物的叶面积、比叶面积和叶干重显著大于阳坡,叶厚度显著小于阳坡,叶干物质含量小于阳坡;阴坡壳斗科植物功能性状的主要环境影响因子是土壤全钾和土壤含水量,全磷是阳坡的主要环境影响因子。阴坡的叶功能性状变异程度小于阳坡,主要是以改变叶干重增加植物体内光合速率和碳积累能力的方式适应阴坡生境;阳坡通过保持较小比叶面积,增加叶面积变异程度来获得更多的资源。退化天坑深陷塘阴坡植物群落演替速度明显快于阳坡,壳斗科植物优势在阴坡逐渐减小,在阳坡仍是优势建群种。     

海南岛山地雨林

海南岛山地雨林位于龙脑香林之上海拔700——1,200米的山地。在外貌和结构上具有典型的雨林特征,但在区系成分方面则与龙脑香林有明显差别。它是在高温多湿、肥沃的山地黄壤等生态条件下发育形成的热带森林,是以具板根的栲、栎、槠、石柯属及陆均松等为特征种,繁多的林下棕榈植物,多层结构的雨林植被。海南山地雨林,可理解为群系组,其下根据综合特征分类,以优势种命名可划分为婆罗椎栗、吊皮栲、陆均松、尖峰栎、龙楠等13个群系(或混合群落)。     

Notes on the Orchid Flora in the Hengduan Mountain Region,China

The Hengduan Mountain Region on the south-eastern fringe of the Qinghai- Xizang (Tibet) Plateau is located in W. Sichuan, N. W. Yunnan and E. Xizang, with a wide area of juxtaposition from the east to the west, the mountains extending and the rivers flowing from the north to the south. In this paper it covers an area from Daojie, Wayao, Yingping, Yangbi, Dali of Yunnan and Dukou of Sichuan in the south, to Banbar, Dengqeu, Shenda of Tibet and Serxu, Dainkog, Shuajingsi and Nanping (Jiuzhaigou) of Sichuan in the north, and from Lharong, Baxoi and Zayü of Tibet in the west, to Maowen, Wenchuan, Mt. Erlang, Mt. Emei and Xichang of Sichuan in the east (Fig. 1.). The Gongga Mountain is the highest in the region, its summit being at an altitude of 7556m, whereas the Dadu River Valley in the eastern part of the area is only 1150 m above sea level. Therefore, the relative height is about 6400 m in the region. The Hengduan Mountain Region is well-known for its various topography, complex natural conditions and rich flora. The floristic composition and features of orchids in Hengduan Mountain Region. 1. The species of orchids are abundant in the region. As we know so far, orchids in the Hengduan Mountain Region comprise 91 genera and 363 species with 9 varieties, and thus it is one of concentration centres of orchids in China, making up 56.17% of the total number of orchids genera in China, only less than in Yunnan and Taiwan, and 34.87% of the total number of orchids species in China, only less than in Yunnan and Sichuan. 2. The orchids genera in the Hengduan Mountain Region are complex in geographical components as indicated below: (1) Four geneva are endemic to China and one of them is endemic to the region. (2) Fourteen genera are of the north temperate distribution pattern, 2 of the Old World temperate one, 18 of the East-Asian one (including Sino-Himalayan and Sino-Japanese) and 3 of the East-Asian-North American one. (3) Twenty one genera belong to the tropical Asian distribution pattern, 3 to the tropical Asian-tropical African one, 13 to the tropical Asian-tropical Australian one, 1 to the tropical Asian-tropical South American one, 8 to the Old World tropical one and 2 to the pantropical one. (4) Two genera are cosmopolitan. The analysis of genera: Fourty eight genera (containing 151 species with 4 varieties) of the tropical distribution occur in the region, among which Calanthe and Cymbidium distributed in the temperate region, and Bulbophyllum and Peristylus in the subtropical part of China are comparatively abundant (with over 10 species), but the other 25 genera are monospecific and 11 genera each contain only 2-3 species. Some epiphytic genera mainly distributed in tropical Asia and belonging to tropical florestic elements, such as Vanda, Luisia, Schoenorchis, Flickingeria, Monomeria, Kingidium, Acampe, Phalaenopsis, Thrixspermum, Eria, Taeniophyllum, and terrestrial genera, such as Aphyllorchis, Collabium, Mischobulbum, Paphiopedilum, Thunia, Brachycarythis, Satyrium, Corybas, Geodorum, Zeuxine, Tropidia, have the Hengduan Mountain Region as the northern limit of distribution. Of 151 species with 4 varieties, 41 species with 4 varieties are endemic to China, and 14 species with 3 varieties of them are endemic to the area, making up 3.86% of the total in the region under discussion. There are 41 genera (containing 189 species with 5 varieties) of the temperate distribution, which occur in the region. Among them Platanthera (22 species with 1 variety), Cypripedium (17 species), Herminium (16 species), Amitostigma (15 species with 1 variety), Orchis (12 species), Hemipilia (8 species with 1 variety), Neottianthe (4 species), Gymnadenia (4 species), Diphylax (3 species), Bletilla (3 species), have the Hengduan Mountain Region as the distribution centre and differentiation centre. Among the 189 species with 5 varieties, 111 species with 5 varieties are endemic to China, and 54 species with 5 varieties are endemic to the area, making up 14.88% of the total of orchids in the Hengduan Mountain Region. Although the number of temperate distribution genera is smaller than that of tropical distribution ones, several points may be mentioned: (1) The Hengduan Mountain Region is distribution centre and differentiation centre of a number of temperate genera in China, and is the northern limit of many genera mainly distributed in the tropics. (2) The number in the former category is obviously larger than that in the latter. (3) Endemic species in the former category in the area are over three times as many as those in the latter. The differentiation of species of the temperate distribution genera is obviously stronger than the tropical ones, which characterizes the orchid flora in the area as the temperate one. The life forms of genera. The orchid flora in the Hengduan Mountain Region so far known comprises 91 genera, among which 51 are terrestrial, 32 epiphytic and 8 saprophytic, thus with the terrestrial one dominant. The analysis of species: The orchid flora in the Hengduan Mountain Region so far known comprises 363 species with 9 varieties. Their distribution patterns and floristic components, to which they belong, are indicated as follows: (1) Fifty four species, belonging to 33 genera, are widespread, covering the whole East Asian Region, but 6 of them are endemic to China. (2) Forty four species, belonging to 27 genera, are the elements of the Sino-Japanese Subregion, but 22 species of them are endemic to China. (3) One hundred and ninety five species with nine varieties, belonging to 53 genera, are the elements of the Sino-Himalayan Subregion under discussion: (A) Four species (i.e. Aphyllorchis alpine, Listera divaricata, L. pinetorum and Oreorchis micrantha) are distributed in the Himalayan Region and S. E. Xizang (Tibet), western part of this region. (B) Twenty five species, belonging to 17 genera, are distributed in N. W. Yunnan and the Himalayan Region (Appendix, 1.). (C) Sixteen species, belonging to 11 genera, are distributed in the Himalayan region and W. Sichuan. Among them 6 species occur only with Mt. Emei as the easternmost limit and 10 species occur in the region west of Mt. Emei. (D) Ten species, belonging to 9 genera, are distributed in the Himalayan region, this region and S. Shaanxi, S. Gansu or S. E. Qinghai. (E) Eight species, belonging to 6 genera, are distributed in the Himalayan region and this region. Among them 6 species have their range extending eastwards to Guizhou and 2 species eastwards to Guangxi. (F) Five species, belonging to 5 genera, having their range extending from this region southwards to N. Burma. (G) One handred and twenty seven species with nine varieties are endemic to China behind discussion. (4) (A) Three species (i.e. Anoectochilus moulmeinensis, Bulbophyllum forrestii and Liparis chapaensis) are distributed in Indo-China, Burma and the region. (B) Nine species, belonging to 7 genera, are distributed in Indo-China, N. E. India and this region. (C) Forty six species, belonging to 21 genera, are distributed in Indo-China, the Himalayan Region and this region (Appendix, 2.). (D) Twelve species, belonging to 11 genera, are distributed in Indo-China and this region (Appendix, 3.) 3. The vicarism is obvious in the orchid flora of the Hengduan Mountain Region. There are 10 species-pairs (in genera Calanthe, Tropidia, Anoectochilus, Mischobulbum, Bulbophyllum, Gymnadenia, Pogonia, Tipularia, Tulotis, Orchis, etc.) of the horizontal vicarism and 7 species-pairs (in genera Epigeneium, Epipogium, Platanthera, Pogonia, etc.) of the vertical vicarism in the region. 4. The endemic species are prolific in the region. In the orchid flora of the Hengduan Mountain Region there are 155 species and 9 varieties endemic to China: (1) Six species are widespread in the whole East-Asian Region. (2) Twenty two species are the elements of the Sino-Japanese Subregion. (3) One hundred and twenty seven species with nine varieties are the elements of the Sino-Himalayan Subregion. Among them 69 species with 5 varieties are endemic to the region (Appendix, 4.), making up 19% of the total in the region; other 58 species with 4 varieties are distributed in the region and neighbouring regions or provinces of it (Appendix, 5.). 5. Remarkable differentiation of the orchid flora in the Hengduan Mountain Region is shown by evident vicarism and abundance of endemic elements, exampled by Amitostigma, Herminium, Orchis, Cypripedium, Platanthera, etc. and one group of Platanthera, which is confined to the south fringe of the Xizang (Tibet) Plateau-Hengduan Mountain Region. The group consists of 12 species, of which one (P. edgeworthii) is distributed in the Western Himalayas from Hazara in Pakistan to Kumaun in India, and all the other 11 species (i.e.P. stenantha, P. bakeriana, P. roseotincta, P. deflexilabella, P. longiglandula, P. exilliana, P. chiloglossa, P. leptocaulon, P. platantheroides, P. clavigera and P. latilabris) occur in China, with 3 of them (i.e.P. deflexilabella, P. longiglandula and P. chiloglossa) endemic to China. According to their structure of gynostemum and form of labellum they belong to Platanthera without question, although they are different from the other members of Platanthera in stigma convex (not concave) and sepals mammillary-ciliate, stigma exhibits a series of evolutionary trends in part of species, from stigma single, convex, elliptic and located near rear of spur mouth (in P. stenantha) to stigma single, suddle, and located near front of spur mouth (in P. bakeriana) and to stigma double, separate and located at front of spur mouth in the other ten species. The group in Platanthera is only confined to the area from the south fringe of the Xizang (Tibet) Plateau to the Hengduan Mountain Region. It seems that the genus has been affected by intense lift of the area, causing variation and differentiation and giving rise to the group due to the long-term natural selection. Mt. Emei in Sichuan Province is the eastern limit of distribution of the group, where there are three spcies, among which two (P. deflexilabella and P. longiglandula) are endemic to the mountains. In addition, among Risleya (1 species), Diphylax (3 species) and Diplomeris (2 species), three genera typical of distribution in the Sino-Himalayan Subregion, Risleya and Diphylax have Mt. Emei as their eastern limit. Eleven species, belonging to elements of the SinoJapanese Subregion, occur only from Japan to Western Sichuan with Mt. Emei as the western limit. Among nine species, belonging to elements of the Sino-Himalayan Subregion, six occur from the Himalayas to W. Sichuan and three of them are endemic to the Hengduan Mountain Region, with Mt. Emei as their eastern limit of distribution. There are eight endemic species and one variety of orchids in Mt. Emei, making up about 11.59% of the total endemic species in the Hengduan Mountain Region. Orchid floristic elements in Mt. Emei are obviously different from those in Mt. Jinfo, the former being mainly of the Sino-Himalayan Subregion, while the latter being mainly of the Sino-Japanese Subregion. From the distribution patterns of the orchid floristic elements in the Hengduan Mountain Region and Eastern China, the Emei Mountain is considered important for drawing a boundary line between the Sino-Japanese Subregion and the Sino-Himalayan Subregion. The discussion may be summarized as follows: the floristic features of the orchid flora in the Hengduan Mountain Region are: (1) rich in species, complex in geographical components, eminent vicarism and differentiation, and prolific in endemic species; (2) terrestrial life form is dominant one; (3) mainly consisting of temperate and subtropical East-Asian elements, es pecially, elements of Sino-Himalayan Subregion, though with some tropical elements and elem-ents of other regions.     

云南哀牢山国家级自然保护区蕨类植物区系地理研究

通过野外调查和资料整理分析,哀牢山国家级自然保护区共有蕨类植物48科,118属,446种(包括变种和变型)。优势科为鳞毛蕨科、水龙骨科和蹄盖蕨科,优势属为耳蕨属、蹄盖蕨属、鳞毛蕨属和卷柏属。区系分析结果表明:该蕨类区系是亚热带性质的区系;热带亚洲成分随着海拔的升高,比例逐渐降低,而中国-喜马拉雅成分随着海拔的升高逐渐增加;地理成分的东西坡差异不明显;该蕨类区系与喜马拉雅地区和热带亚洲的关系较密切,而与日本的关系较疏远;该蕨类区系具有较丰富的中国特有成分;哀牢山明显处于滇西北、滇东南这两大中国特有多样性中心之间,成为联系的纽带。     

Study on the Floristic Phytogeographical Differentiation of Xizang Tibet

The geoecological conditions of Xizang (Tibet) are very complicated. An approach on the floristic phytogeographical differentiation of Xizang has been made in the present paper with a quantitative floristic method. According to areal types of the species the flora of Xizang may be classified under five major geoelements: the north temperate zone geo-element (N), the Central Asiatic geoelemcnt (C), the Qinghai-Xizang Tibetan Plateau geo-element (T), the Sino-Himalayan geo-element (SH) and the tropical geo-element (Tr). Different diagrams of spectra of floristic elements of Xizang are presented. Four cross-sections were chosen for illustrating the regional differentiation of spectra of floristic elements of Xizang. It is obvious that the SH-geo-element prevails in the Eastern and Southeastern Xizang and the Trgeo-element is confined at lower elevation of the southern flanks of the Himalayas. On the contrary, on the Plateau proper the Tgeoelement dominates and the C-geo-element plays a significant role in the northwestern part of Xizang. It corresponds to the following horizontal zones of vegetation from southeast to northwest: montane forest-alpine meadow-alpine steppe-alpine desert. An example at the southern slopes of the Eastern Himalayas has been taken to investigate the vertical variation of the spectra of floristic elements, the boundary between the both subbelts of the montane evergreen broad-leaved forest belt at an elevation of 1,800 m has been proposed as the upper limit dominated by the tropical geo-element. On the basis of dominance spectra of the fioristic elements in the grid-square system floristic boundaries are defined, which separate different floristic regions from one another, thereafter a floristic division of Xizang has been discussed. There are the sub-region of the "Himalayan flanks belonging to the Indo-Malaysian sub-kingdom of the Palaeotropical kingdom, the Sino-Himalayan sub-kingdom and the Qinghai-Xizang Plateau sub-kingdom of the Holarctic kingdom.     

云南省小黑山自然保护区种子植物区系研究

小黑山自然保护区有野生种子植物170科787属2195种。分析表明该区种子植物区系的地理成分复杂,联系广泛。热带性质的属有506属,占总属数的68.6%,温带性质的属有224属,占总属数的30.4%。热带性质的种890种,占总种数的40.9%,温带性质的种有1267种,占总种数的58.3%。表明该地区植物区系具有明显的亚热带性质,同时深受热带植物区系的影响。植物区系来源主要由东亚成分、热带亚洲成分(印度—马来西亚成分)、中国特有成分三部分融合而成。特有现象明显,有东亚特有科5科,中国特有属6属,中国特有种778种,占种总数的35.8%,而云南特有种有355种,占中国特有种的45.6%。保护区还拥有众多的珍稀濒危植物。     

高黎贡山北段种子植物区系研究

高黎贡山北段种子植物种类十分丰富,共记载野生种子植物172科,778属,2514种及302变种(亚种),是植物多样性最为丰富的地区之一。区系成分分析表明:1)本区种子植物区系的性质具有鲜明的温带性,并深受热带植物区系的影响,区系地理成分复杂、联系广泛;2)现代种子植物区系是在古南大陆热带亚洲植物区系的基础上,由古南大陆成分及古北大陆成分在漫长的地质历史过程中融合发展而来,许多源于印度-马来、北温带(特别是东亚)的成分在此都产生了较为丰富的特有类群,它们共同演变成今天的植物区系外貌;3)种子植物区系具有明显的水平和垂直替代现象,间断现象也较为显著,主要表现为滇西北-滇东南间断分布或在此线西南侧连续分布;4)种子植物区系的特有现象十分丰富,物种分化强烈,新老兼备,而以新生的进化成分为主,由此表明高黎贡山北段在保存古老成分的同时,又分化出许多新生成分,它是一个孕育新特有现象的重要舞台。     

南海岛屿种子植物区系地理的研究

本文通过实地考察,广泛收集前人的研究资料,概述了南海岛屿地区的自然条件和植被,对南海岛屿种子植物的区系组成、特点、分布区类型、特有现象和替代现象等进行了较详细的分析,并与邻近植物区系进行了比较研究。同时,根据区内植物分布的特点和自然条件特征划分为５个植物区系小区,最后对南海岛屿地区植物区系的起源与演化进行了讨论。     

贡嘎山东坡植物区系的垂直分布格局

为了探讨贡嘎山植物区系的垂直分化特征及其与周边地区植物区系的联系,结合样带法与样方法,对贡嘎山东坡垂直植被带进行了调查,统计得出各垂直植被带的科、属的物种数量,分析了科、属、种级区系成分的构成及其沿海拔梯度的分布格局,并对各垂直植被带区系的相似性进行了聚类分析。结果表明：1)贡嘎山植物区系在整体上具有温带性质,但在干旱河谷地带,热带和温带区系成分的比例相当：热带成分的构成和分布反映古热带和古地中海区系的残遗性影响;2)东亚(含亚型)和东亚-北美成分对贡嘎山中部森林植物区系的影响最大,这些成分以温带古老性质为主;3)北温带成分是贡嘎山植物区系的主体之一,对青藏高原隆升以来贡嘎山植物区系进化类群和特有成分的发展有主要贡献,代表区系的年轻组分;4)中国特有种类型多样,占不同垂直植被带物种数量的40％-65％,其比例随海拔上升而增大。各类型比例的垂直变化突出反映了贡嘎山及横断山脉中海拔地段的植物区系与华中地区的联系,以及高海拔地段与青藏高原及东喜马拉雅的区系之间的联系。本文还就贡嘎山在生物地理分布上的意义以及贡嘎山和横断山脉植物区系特有性的性质进行了讨论。     

梵净山种子植物区系特征及植物地理学意义

梵净山为地处云贵高原向湘西丘陵过渡斜坡区,是武陵山脉的最高主峰,面积约为77 514 hm~2。该研究针对当地野生种子植物区系的问题,主要通过对种子植物科属种水平的地理成分、区系古老性、区系过渡性等区系特征进行了统计和分析。结果表明:(1)该区物种丰富、地理成分复杂,共有野生种子植物163科843属2 584种,中国特有种1 010种(含梵净山特有种46种),其中属的热带、温带地理成分比例相当,热带成分略占优势。(2)该区植物起源古老,保存有梵净山特有裸子植物梵净山冷杉、长苞铁杉、粗榧、水青树、伯乐树、领春木等大量古老树种。(3)该区与临近区系交汇、渗透现象明显、过渡性质突出,经初步确定以梵净山为典型分布边界点的植物共有120科197属288种,分别有103种、62种、87种、36种以梵净山地区为分布的北界、南界、东界和西界,即梵净山更多的阻碍了热带、亚热带植物的北迁和中国—喜马拉雅成分的东扩。(4)该区常绿树种与落叶树种并茂发育,热带成分与温带成分竞争激烈。因此,梵净山在中国植物区系甚至东亚植物区系中具有非常重要的意义。     

云南常绿阔叶林的植被地理研究

云南具有极其丰富的生物多样性和以常绿阔叶林为优势的植被类型。该研究利用6个基于样方层面的1 hm²样地资料, 以及通过对整个植被类型的植物区系的调查, 对云南常绿阔叶林植被型的3个植被亚型(季风常绿阔叶林、半湿润常绿阔叶林和中山湿性常绿阔叶林)的生态外貌特征、植物区系组成及其生物地理演化进行了研究。在样方层面, 尽管这3个常绿阔叶林在树种组成上优势种均为壳斗科、樟科和山茶科植物, 但它们在种类组成、多样性、生态外貌和生物地理特征上呈现多样化。分布在南部及西南部的季风常绿阔叶林物种组成极其丰富, 具有热带森林的生态外貌, 并以热带亚洲分布种为优势种。主要分布在云南高原的半湿润常绿阔叶林和云南中部和北部山地的中山湿性常绿阔叶林具有亚热带常绿阔叶林的生态外貌特征和以中国-喜马拉雅及中国特有种占优势, 是中国西南独特的植被类型。在植被亚型层面, 这3个常绿阔叶林的植物区系(包括所有生活型的种子植物)中种数最多的科, 按地理成分均为世界分布型的科, 含种数较少的科则为其他各种分布型的科。半湿润常绿阔叶林和中山湿性常绿阔叶林的植物区系, 热带分布属分别占总属数的44.91%和44.04%, 温带分布属占46.29%和48.19%, 其中北温带分布属比例最高, 分别为18.36%和19.95%。季风常绿阔叶林植物区系则显示了不同的地理成分格局: 热带分布属占总属数的78.05%, 并以热带亚洲分布属占最高比例。通过对这3个常绿阔叶林的比较发现, 半湿润常绿阔叶林和中山湿性常绿阔叶林除生态外貌特征有一定区别外, 在植物区系组成和地理成分上很接近, 它们在种的组成上, 与季风常绿阔叶林的类似性仅为17.1%和15.4%。季风常绿阔叶林因其在植物区系和生态外貌上与后二者区别明显, 建议在云南植被分类上划分一个独立的植被型, 它是东南亚低山常绿阔叶林分布在中国西南部热带北缘山地的一个植被类型。结合云南的地质历史和古植物学资料, 认为云南的常绿阔叶林及其植物区系受晚中新世以来的地质历史事件深刻影响。半湿润常绿阔叶林是中国西南独特而特有种丰富的植被类型, 由于严重的人为干扰破坏, 现已片段化或成为萌生灌丛状, 应给予优先保护。