海南竹类的地理分布及区系特征

通过对海南岛竹类区系地理成分进行统计、分析和对其分布、与邻近地区竹类区系关系的探讨,其区系特征归纳如下:1.拥有丰富的特有成分。2.区系的热带性质明显。3.分布上差异显著。4.区系原始、古老。5.与毗邻的广东竹类区系联系较多。     

On Genera Endemic to China and Occurring in Xizang Plateau Flora

The Xizang (Tibetan) flora with numerous endemics is of importance in Chinese flora. According to recent statistics there are in Xizang 27 genera of spermatophytes endemic to China, being only 2.25% percent of the total number of genera in the Xizang flora. Four of them are regarded as palaeoendemics (14.81%) and the others as neoendemics (85.19%). These endemic genera, of 30 species and 3 varieties, belong to 17 families, of which, Umbelliferae contains 6 genera, 7 species and 3 varieties; Compositae has 6 genera and 7 species, and Gentianaceae 1 genus and 2 species. All the other families each comprises one genus with a single species. The cosmopolitan families together comprising 14 genera with 15 species have the highest perecentage (52.92%) and the tropical ones (5 families, 5 genera with 5 species) come to the next (29.42%), followed by the temperate ones (3 families, 10 genera with 10 species) (17.66%). It shows that these endemic genera are obviously related to the tropical flora and temperate one in essence. According to the number of species, the genera endemic to China and occurring in Xizang flora may be grouped as fallows. Monotypic endemic ones 14 (51.85%) Ditypic endemic ones 6 (22.22%) Oligotypic endemic ones 4 (14.81%) Small endemic ones 3 (11.11%) The formation of the endemic genera is correlated with the topography, climate and environmental conditions, and they may have resulted from the diversification in geography and climatic influence for a long time. The southeastern part of Xizang Plateau is of very diverse ecological conditions, with the adequate precipitation, which may explain the concentration of these endemic genera in this region. The largest similarity coefficient (38.30%) of the genera endemic to China and occurring in Xizang is with those in Qinghai Plateau, next, with those in Yunnan and in Sichuan provinces (both 27.60%), which shows that these endemic genera are related to the floras of the regions mentioned above. The difference in the horizontal distribution of these endemic genera is obviously between the southern and northern parts of Xizang Plateau. The vertical distribution of the genera is also rather obvious, from 800 m to 5200 m above sea level, but concentrated in the zone of 3000 m to 4500 mm. Therefore their occurrence in Xizang is not only affected by the historical environmental conditions but also controlled by the horizontal and vertical distribution. The origin and evolution of some endemic genera, such as Psammosilene, Parateropyrum, Sphaerotylos, Salweenia, Ajaniopsis, Xizangia, Sinoleontopodium, are discussed in this paper. Parateropyrum, a monotypic palaeotropic endemic, belongs to the tribe Atraphaxideae including Atraphaxis, Calligonum and Pteropyrum. It may be a comparatively advanced group in the tribe, and is closely related to the genus Pteropyrum which is distributed in western Asia. The genus Parapteropyrum has possibly survived as a palaetropic-tertiary relic in this region. Sphaerotylos, a member of the subtribe Sphaerotylinae, the tribe Boehmerieae in the family Urticaceae, is a comparatively primitive genus in the tribe Boehmerieae so far known. As the other subtribes, such as Boehmerinae, Sarconchlamydinae, Orecnidinae and Maoutinae, are distributed in the tropics, rarely in the subtropics, the genus is no doubt a palaetropic -tertiary relic. Sinoleontopodium, belonging to the tribe lnuleae in Compositae, is also related to the genus Leontopodium. It is probable that the genus Sinoleontopodium arised later than the other. We come to the conclusion that the southern part of Xizang Plateau is also one of thecentres of the origin and differentiation of genera endemic to China.     

Relationships Between the Bryoflora of Mt. Wuyi,SE China,and Those of Neighbouring Mountain Regions

Mt. Wuyi, located at 27°37‛-27°54‛ N, 117°27‛-117°51‛ E, is the highest mountain in South-East China. Its main peak, Huanggangshan, is 2158 m above the sea level. In 1955, P. C. Chen organized the first expedition to Mt. Wuyi, and the authors investigated the different ravines and the forests of that area in 1976 and from 1979 to 1984 respectively. Up to now 355 species of the bryophytes have been found in Mt. Wuyi. I. The influence of the factors of geological history on the bryoflora of Mt. Wuyi Fujian Province, belonging to Cathaysian, one of three Chinese ancient lands, was a part of ocean until the end of the lower Tertiary. In the early Devonian, Fujian uplifted above the sea level, but it submerged in the sea later, and then uplifted above the sea level again in the upper Triassic. By the end of the lower Triassic the Himalayan movement influenced the paleogeography of China deeply, and the eastern and central mountains of Fujian uplifted again. In the Tertiary, Fujian was influenced by the hot maritime weather, so the tropical evergreen forests existed in southern Fujian at that time. The conclusion was made by Z. B. Zhao in 1983 after his long period of study on geological history of Fujian Province since the Yanshan movement. According to the morden geographical distribution of Chinese bryophytes, it seems that the above influence might be related to the bryophytes of Mt. Wuyi and also the southern part of Zhejian Province. By the end of the Tertiary the weather became cold in most parts of China. Since then the cold weather and hot weather alternated several times. One kind of the endemic elements of the bryoflora formed in the area from the south-eastern coast of China to the southeastern Xizang (Tibet), including Japan. They are not specialized at the family level or closely related to each other, but they have similar distribution and belong to different families. In the Quaternary, Mt. Wuyi gradually uplifted following the Himalayan movement. As the weather cooled down in the upper part of the mountain, deciduous broad-leaved and needleleaved trees increased there. Meanwhile, temperate genera and species of the bryophytes spread and invaded South China and entered Mr. Wuyi. Rhytidiadelphus and Hvlocomium probably began to grow in Mt. Wuyi at that time, and their distribution is quite different from their primary one. On the other hand, a part of tropical and subtropical bryophytes might enjoy the changed weather and environment in the Quaternary and existed in a few small localities of Mt. Wuyi, and the genera Haplomitrium, Endotrichella and Floribundaria are probably their representatives. From the point of view of geological history we are now living in the interglacial period and the present natural conditions will last continuously, so they will steadily influence the bryoflora of Mt. Wuyi in a long period of time. 2. Essential characteristics of the bryoflora in Mt. Wuyi Due to the geographical position and the other factors of Mt. Wuyi the bryoflora is represented by numerous tropical and subtropical elements (34.1%), but the East-Asiatic endemic ones (79.2%) are characteristic of the bryoflora in Mt. Wuyi (Tab. 1). The tropical and subtropical families of the bryophytes, found south of Changjiang (Yangtzi) River, are Haplomitriaceae (1 genus, 3 species), Porellaceae (2 genera, 8 species), Frullaniaceae (2 genera, 10 species), Lejeun eaceae (21 genera, 35 species), Trachypodaceae (3 genera, 4 species), Meteoriaceae (10 genera, 17 species), Neckeraceae (5 genera, 8 species) and Hookeriaceae (3 genera, 3 species). The above 8 families, including 46 genera and 85 species, represent about 1/4 genera (24.3%) and less than 1/4 species (23.9%) of the bryoflora of Mt. Wuyi. Most species of East-Asiatic elements show very close relationships with Japan, and are widely distributed from the low altitude of Mt. Wuyi to the summit of Mt. Huanggangshan. However, the Holarctic species (26.8%) are also important elements of the bryoflora in Mt. Wuyi, showing its transition nature, although it is located in the subtropics. Moreover, the in fluence of the Himalayas also exists in Mt. Wuyi, and the Himalayan elements cover 14.4% in the bryoflora of Mt. Wuyi. The similarity coefficients between the bryofloras of Central and South America, Africa and Oceania and that of Mt. Wuyi are from 5.0-9.2% respectively. The endemic species are not very many and cosmopolitan species are only 7 there. In 1958, P. C. Chen designated Mt. Wuyi as “the transition region of South and North China rich in East-Asiatic genera and species”. His very important conclusion is essentially in accordance with the fact of the bryoflora on Mt. Wuyi. Recently, some of the new records fur ther show the characteristics of the bryoflora in Wuyi. Two facts are worth being mentioned. One is that East-Asiatic genera are only five in Mt. Wuyi. However, there are 9 East-Asiatic genera in Mt. Huangshan more than in Mt. Wuyi; 4 East-Asiatic genera are recorded in Mt. Shennongjia. The other is that epiphyllous liverworts in Mt. Wuyi, consisting of 7 families, 21 genera and 36 species, are less than on Hainan Island and Xishuangbannan, located in the tro pics in China. 3. Comparison between the bryoflora of Mt. Wuyi and those of the neighbouring regions As China covers a very large area, bryofloristic elements are quite different in the diffe rent regions. In this section, we are concentrated on making a comparison between the bryof loras of Mt. Wuyi and the regions belonging to the Central China of the bryoflora named by P. C. Chen. Huaping Forest Region, Guangxi Zhuang Autonomous Region in South China, with both latitute and altitude very similar to Mt. Wuyi, is included in this comparison (Fig. 1). According to the rough estimation, the similarity coefficient of moss genera between Mt. Wuyi and Huaping is 56.3%, and those between the mountain and southern Zhejian and Mt. Huangshan, Anhui, are 62.7% and 51.6% respectively, while the similarity coefficient of the genera of the mossfloras between Mt. Shennongjia and Mt. Wuyi is 46.8%. Table 2 shows the statistics of mosses in Mt. Wuyi and the others, but the bryoflora of Huaping needs further study However, it is very interesting to note that Haplomitrium and Pleurozia of liverworts are both found in Mt. Wuyi and Huaping Forest Region, and the similarity coefficient between the mossfloras of Mt. Wuyi and Zhejian Province is also higher than those mentioned above. Tropical and subtropical elements reduce towards the north in China, and temperate ones increase. Huaping is located in the south, and, as expected, some tropical and subtropical genera such as Hookeriopsis and Symphyodon have been found there, but not in Mt. Wuyi; several temperate genera, such as Schwetschkeopsis and Fauriella, have been recorded in Mt. Huangshan, but not in Mt. Wuyi. For some unknown reasons, Octoblepharum and Neckeropsis are only found in southern Zhejiang, but not in Mt. Wuyi. Mt. Shennongjia, with its main peak over 1000 m higher than that of Mt. Wuyi, is located in its northwest, and more than ten temperate genera, such as, Ceratodon, Aulacomnium Myurella, Bryonoguchia and Abietinella have been found there. Generally, Mt. Wuyi belongs to the central subtropical region of China, and East-Asiatic endemic genera are the main elements of its bryoflora, but the bryoflora also consists of tropical and subtropical elements with some temperate ones. 4. East-Asiatic endemic genera in the bryoflora of Mt. Wuyi In the bryoflora of Mt. Wuyi, one of the main elements, East-Asiatic endemic genera, should not be neglected (Tab. 4). East-Asiatic endemic genera in Mt. Wuyi (five) are less than in Mt. Huangshan and Mt. West Tianmu, although the positions of the latter two are very close to Mt. Wuyi. East-Asiatic endemic genera of liverworts are Trichocolea and Macvicaria so far found in Mt. Wuyi, and the mosses are Myuriopsis, Meteoriella, Pseudospiridentopsis (Fig. 1). Myuriopsis is only distributed in Taiwan Province and Mt. Wuyi, and the other four are distributed in Mt. Huangshan or Mt. West Tianmu, and also in Taiwan, besides in Mt. Wuyi. About thirty EastAsiatic endemic genera have so far been known in China, which means that about one sixth of East- Asiatic endemic genera of the bryophytes occur in Mt. Wuyi. We may notice that nine and seven East-Asiatic endemic genera of the bryophytes have been recorded in Mt. Huangshan and Mt. West Tianmu respectively. In Mt. Shennongjia, Central China, there are four East Asiatic endemic genera, but only two have been found in the Huaping Forest Region, South China. In Mt. Dinghua, located south of Mt. Wuyi, on East-Asiatic endemic genus of the bryophytes has so far been found. East-Asiatic endemic genera of the bryophytes are mainly limited to China, Korea and Japan, including the East Himalayas, rarely occur in South Asia, Siberia of the Soviet Union. Therefore, these genera enjoy a warm and moist environment. In Mt. Wuyi, all the East-Asiatic endemic genera are monotypic ones with a disjunct distribution. Now in Taiwan Province five of six recorded East-Asiatic endemic genera are common to Mt. Wuyi. In Japan, about eleven, i.e. one third of, East Asiatic endemic genera so far found are common to China, which shows a long history of the phytogeographical relationships between Japan and China. East Asiatic endemic genera of the bryophytes might therefore exist on islands of Taiwan Province and Japan before they were separated from the mainland of Asia. However the fossil evidence is still lacking in the bryophytes, so we are not able to discuss about the distribution area and the distribution center of the East-Asiatic bryoflora in detail. The above estimation is more or less related to geological history, and we assume that the East-Asiatic endemic genera have existed at least since the end of the Tertiary. Starting from the Quaternary, the climatic change during glacial epoch has been possibly the most important factor affecting the bryoflora in Asia, and the upheaval of the Himalayas has stimulated the diversity and the specialization of the bryophy tes. Considering these factors, East-Asiatic endemic genera might be the “Tertiary fossil plants”. Another problem is difficult to explain, because Mts. Huangshan, West Tianmu and Shen nongjia were once influenced by glaciation directly, although Chinese geologists hold different views. However, no evidence of glaciation has been found in Mt. Wuyi. It is worth to study the close relationships between Mt. Wuyi, Mt. Huangshan and Mt. West Tianmu, where is the distri bution center of the East-Asiatic endemic genera. The above three mountain regions share half of the East-Asiatic endemic genera, and about 32% genera of the others are found in two of them (Fig. 2). Myuriopsis, one of the East Asiatic types, was only recorded in Taiwan Pro vince, Japan and Korea. Neodolichomitra, occuring in Taiwan Province, is endemic to China. More or less the differentiation has taken place in Mt. Huangshan, Mt. West Tianmu and Mt. Wuyi. The number of the East-Asiatic endemic genera is smaller in Mt. Wuyi, so it is possibly located on the border of the distributional center of the East-Asiatic endemic genera. Moreo ver, three of four East-Asiatic endemic genera in Mt. Shennongjia are also found in Mt. Huang shan and Mt. West Tianmu, but the other East-Asiatic genus in Mt. Wuyi is common to the mountain areas in SW China, the Qinglin Range of NW China, and the isolated mountain areas of NE China. Considering all the characteristics of the bryoflora of Mt. Shennongjia, we assume that Mt. Shennongjia may belong to another distribution center, including SW part of Sichuan Province, and the other neighbouring mountains.     

The Floristic Characteristics and Geographical Distribution of the Rosaceae in Xizang

The Rosaceae is one of the five largest families of Xizang flora, consisting of 30 genera with 242 species, the total number of species is slightly less than those of Compositae, Graminae, Leguminosae and Ericaceae in Xizang, amounting to 62.5% of the total number of genera and 28% of the total number of species of the rosaceous flora in China. The four subfamilies of Rosaceae including primitive, intermediate and advanced groups have been found in Xizang. These groups consist of 11 types of floristic elements, i.e. 4 genera belong to cosmopolitan, 9 genera belong to North Temperate, 3, E. Asian-N. American, 3 Sino-Himalayan, 3 Sino-Japanesa, 2 Old World Temperate, 1 Temperate Asian, 2 Mediterranean-W. and O. Asian, 1 C. Asian, I Tropical Asian and 1 endemic to China. It is obvious that Rosaceae in Xizang comprises holarctic, Ancient Mediterranean and paleotropical elements, among which the temperate components are the most dominant. The characteristics of the floristic composition of Rosaceae in Xizang may be summarized as follows: (1) Xizang abounds in both genera and species of the family which are diverse in forms, including the primitive, intermediate and advanced groups, (2) The geographical elements are rather complex, mostly belonging to the temperate, among which the Sino- Himalayan components and the elements endemic to China are dominant, (3) The proportion of plants endemic to China and distributed in Xizang is much higher than those endemic to Xizang itself, but there exist newly arisen species and infraspecific forms or varieties which show that the speciation is apparently still active in Xizang. The rosaceous flora of Xizang is a combination of old and new floristic elements, based on the old floristic components, affected by the upheaval of the Himalayas, the differentiation and speciation have been taking place in the long history. The geographical distribution of Rosaceae in Xizang may be divided into 5 regions, i.e. the northeastern, southeastern, southern, northwestern and northern. The rosaceous plants are most abundant in the southeastern area, next in southern area, fewer in the northeastern and very rare in the northwestern and northern regions. The general tendency of the distribution of Rosaceae in Xizang is that the number of species gradually decreases from the southeast to the northwest and the habit gradually changes from trees, shrubs and herbaceous plants in the southeast to cushion-like scrubs and dwarf perennial herbs in the northwest. These facts clearly show that the uplift of the Himalayas has deeply affected the phytogeographical distribution of Xizang Rosaceae. The rosaceous flora of Xizang has close relationships with those of the adjoring regions, i.e. Yunnan and Sichuan. Besides, it is connected with floras of Nepal, Sikkim, Bhutan nothern Buram and nothern India, but silghtly influenced by the Ancient Mediterranean flora.     

高黎贡山南段种子植物区系的特有现象

高黎贡山南段是全球生物多样性研究热点地区之一,迄今计有野生种子植物192科878属2 807种.这一区域不仅植物的种类丰富,而且特有现象较为显著.其中东亚特有科8个、中国特有属17个、中国特有种1 085个、云南特有种305个、高黎贡山南段特有种82个.特殊地质历史和生态环境,使得高黎贡山南段既保留了许多古老特有成分,又孕育了许多新生特有成分.     

The characteristics and possible origin of the bryoflora of the southern flank of the East Himalayas

In the south-east and south Xizang, in cluding Medog, Zayü some western separate valleys Yadong, Kama near Zentang in Dinggye, Boqu near Zham in Nyalam and Gyirong, a mild climate prevails because of the very high mountains and the very deep valleys. According to our preliminary survey, 4/5 of the genera and 7/10 of the species, i.e. approximately representing all families and genera of the tropical and subtropical bryofliora of Xizang, are restricted to these localities below the altitude of 2,300 meters. It almost agrees with the previous presumption that the Tsangpo gorge is the line of connection between two paleoeontinents—Laurasia and Gondwana. Moreover, the bryoflora of these localities, besides the Indo-Malasian elements and East Asian elements as the main components, has at least about 40 genera in common with south America, Australia and Africa. According to the historical phytogeographical point of view, the distribution range of centain genera is formed through a period of long historical development. The same is true for the area of different species, although they are found in widely separate areas right now, yet they might have once a continuous distribution in certain historical age. The Indian plate collided against the eastern part of Laurasia and afterwards the Australasian plate moved to the north. All these might have dispersed the Gondwana elements as far as to the southeastern part of Xizang. It is very interesting to note that of the 32 genera of bryophytes endemic to East Asia, 13 have recently been found in the southeast and south Xizang and also in the neighbouring regions, i.e. Yunnan, Sichuan, where there are many genera being in common with southeast and south Xizang and also highly concentrated in distribution. This may suggest that the Himalayas, being the highest and youngest mountain range, have changed the atmospheric circulation, and have created a new ecological condition between tropical and frigid zones, which have given the distribution of the newly formed genera a suitable circumstance to survive. It may be presumed that the region covering counties Medog, Zayü, Yadong etc. in southeastern and southern parts of the Himalayas is a new center of distribution of bryophytes under the influence of the up-heaval of the Himalayas.     

澳门的两栖和爬行动物

澳门已知两栖爬行动物（不包括海产种类） ３ 目１４ 科２８ 属３８ 种, 其中两栖动物１ 目４ 科５ 属９ 种, 爬行动物２ 目１０ 科２３ 属２９ 种。物种密度高达１７７１５－６／１０４ｋｍ２ 。均为东洋界成分, 以南中国型占优势, 其次为印度马来型、印度支那型和泛东洋界型。与广东省的生物相似值为０－４３, 与香港的生物相似值为０－５４ 。在动物地理区划上应属东洋界中印亚界华南区的东南沿海亚区。     

Endemism in the Flora of China—Studies on the Endemic Genera

China, under highly varied ecological conditions resulted from wide latitudinal and altitudinal ranges and from the adequate precipitation, has developed a very rich flora of great diversity. As far as flowering plants are concerned, there are 2980 genera, 214 of which, belonging to 64 families, are endemic. Among these endemic genera, there are 9 genera of taxads and conifers, 19 genera of monocots and others of dicots. Of the approximately 129 herbaceous endemic genera in the Chinese flora as a whole, about 22 (17%) are annual and 107 (83%) are biennial or perennial. In the present paper the ecological distribution, the nature of endemic genera and the centers of endemism are discussed. 1. Three types of endemic genera are distinguished, neoendemics, palaeoendemics and active epibiotics, The endemic genera in the flora of China are, for the most part, considered to be very old ones, and most of them are of temperate nature. 2. the degree of endemism in our 22 floristic regions is shown in Figure 1. The areas richest in endemic genera in the Chinese flora as a whole are the 13, 16 and 17 regions. The poorest are the 2, 4, 9 and 10 regions, and no one in the 1 and 3 regions These results on floristic richness are of general applicability. As shown in table 1, the difference in the degree of endemism among the seven Chinese floristic subkingdoms are most pronounced. 101 endemic genera are known to occur in one subkingdom, 72 to occur in two subkingdoms, and 3 to occur in four subkingdoms, only one genus widely distributed in five subkingdoms. However, there is no genus occurring in seven subkingdoms. The difference in the degree of endemism in each subkingdom reveals that the distribution of endemic genera is not well-distributed in the Chinese flora as a whole. Analysis of the vertical distribution of the 200 endemic genera of the Chinese flora bears out that there is no evident increase in endemism as a whole with altitude. 3. Three centers of endemism are found (Fig. 2). These are as follows: a). Eastern Sichuan-western Hubei center. b). Southeastern Yunnan-western Guangxi center. c). Western Sichuan-northwestern Yunnan center. The degree of endemism andcharacters of endemic genera in each center are discussed.     

中国热带生物地理北界的建议

以前多个关于中国热带北界的建议由于依据的指标和学科不同,存在很大的差异。我们基于202个中国地理区的植物区系和气象资料,对中国种子植物属的地理成分分布格局及其与气候、经纬度分布的关系进行研究,同时依据覆盖中国北纬30°以南地区的135个地方植物区系资料,对种子植物属的地理成分分布格局进行了研究。结果显示,在中国植物区系中,依据种子植物区系科和属的地理成分(即分布区类型),发现热带分布属中80%以上的区域基本上在中国南部和东南部北纬22°30'以南。在这条界线以南地区,位于基带(低海拔或水平地带性区域)的原始植被为热带森林(热带雨林、季雨林),并且具有在中国分布的典型热带植物科,但在中国西南部,热带森林沿云南西部可达到北纬24°30',在西藏南部的深切河谷可达到北纬29°。这条界线与中国的热带雨林、季雨林区划的北界相符合,亦与植物区系分区上的泛北极植物区系与古热带植物区系的地理分界线相吻合。结合中国植被和植物区系区划,我们建议将北纬22°30'作为中国南部和东南部的生物地理热带北界。这条热带北界比气候上的热带北界(21°30'N,年积温8000℃以上)更北,这暗示中国热带地区在历史上可能曾达到更北的范围,支持在古生态学研究上提出的全新世中期中国东部地区热带和亚热带常绿阔叶林曾北移的结论。     

浙江百山祖自然保护区种子植物区系分析

统计分析了浙江庆元百山祖自然保护区的种子植物区系。该区共有种子植物 16 7科、70 0属、 15 45种 (含种下分类群 )。科的分布区类型以泛热带分布最多 ,达 33 5 % ,热带分布的科多于温带分布的科 (75 4 4) ,16个表征科中 ,大多也是以热带分布的科 ;本区以单种属和寡种属为主 ,属的分布区类型以泛热带分布最多 (2 0 2 % ) ,其次是北温带分布(13 9% ) ,热带分布与温带分布的属几相当 (30 4 317) ;种的分布区类型以中国特有种最多(4 8 4 % ) ,其次是东亚分布 (2 3 9% )和热带亚洲分布 (13 6 % )。以中国区系分区标准 ,将特有分布种划分成 9个分布亚型 ,其中以华东 -华中 -华南分布最多 (2 5 9种 )。百山祖自然保护区种子植物丰富 ,区系起源古老 ,地理成分多样 ,具有明显的华东南缘山地植物区系特征 ,并且拥有众多特有、珍稀濒危植物     

试论中国种子植物特有属的分布区类型

中国种子植物特有属是局限分布于中国行政区域范围内的植物成分,就其分布特点看,集中分布于中国南部亚热带广阔区域。由于中国地域广袤,虽然大多数特有属分布在东亚自然地域范围内,但南部特有属的分布范围已进入古热带植物区的马来亚森林植物亚区的北部,而西部的特有属的分布范围已进入青藏高原地区。局限于不同地域分布的特有属,各自的起源发生、所经历的地质历史过程存在一定差别。本文以自然地理区划作为研究中国种子植物特有属分布区类型的依据,将中国特有属分布区类型划分为中国东部和中部特有分布变型、中国南部特有分布变型、中国西部特有分布变型和中国北部特有分布变型4类。其中中国南部特有分布变型所含特有属为热带区系成分,其它3个特有分布变型所含特有属为温带区系成分。这样能较客观地反映中国特有属的自然地理特征,有利于研究局部地区植物区系的地质历史演变过程。     

A previously unrecognized radiation of ranid frogs in Southern Africa revealed by nuclear and mitochondrial DNA sequences

In sub-Saharan Africa, amphibians are represented by a large number of endemic frog genera and species of incompletely clarified phylogenetic relationships. This applies especially to African frogs of the family Ranidae. We provide a molecular phylogenetic hypothesis for ranids, including 11 of the 12 African endemic genera. Analysis of nuclear (rag-1, rag-2, and rhodopsin genes) and mitochondrial markers (12S and 16S ribosomal RNA genes) provide evidence for an endemic clade of African genera of high morphological and ecological diversity thus far assigned to up to five different subfamilies: Afrana, Cacosternum, Natalobatrachus, Pyxicephalus, Strongylopus, and Tomopterna. This clade has its highest species diversity in southern Africa, suggesting a possible biogeographic connection with the Cape Floral Region. Bayesian estimates of divergence times place the initial diversification of the southern African ranid clade at approximately 62-85 million years ago, concurrent with the onset of the radiation of Afrotherian mammals. These and other African ranids (Conraua, Petropedetes, Phrynobatrachus, and Ptychadena) are placed basally within the Ranoidae with respect to the Eurasian groups, which suggests an African origin for this whole epifamily.     

A biogeographical study on tropical flora of southern China

The tropical climate in China exists in southeastern Xizang (Tibet), southwestern to southeastern Yunnan, southwestern Guangxi, southern Guangdon, southern Taiwan, and Hainan, and these southern Chinese areas contain tropical floras. I checked and synonymized native seed plants from these tropical areas in China and recognized 12,844 species of seed plants included in 2,181 genera and 227 families. In the tropical flora of southern China, the families are mainly distributed in tropical areas and extend into temperate zones and contribute to the majority of the taxa present. The genera with tropical distributions also make up the most of the total flora. In terms of geographical elements, the genera with tropical Asian distribution constitute the highest proportion, which implies tropical Asian or Indo‐Malaysia affinity. Floristic composition and geographical elements are conspicuous from region to region due to different geological history and ecological environments, although floristic similarities from these regions are more than 90% and 64% at the family and generic levels, respectively, but lower than 50% at specific level. These differences in the regional floras could be influenced by historical events associated with the uplift of the Himalayas, such as the southeastward extrusion of the Indochina geoblock, clockwise rotation and southeastward movement of Lanping–Simao geoblock, and southeastward movement of Hainan Island. The similarity coefficients between the flora of southern China and those of Indochina countries are more than 96% and 80% at family and generic levels, indicating their close floristic affinity and inclusion in the same biogeographically floristic unit.     

广东山区兰科植物区系的研究

初步统计 ,广东山区共有兰科植物 71属 2 0 8种。其中以热带分布属 4 7属 ( 66.2 % )为主 ,占绝对优势 ,其次为热带—亚热带属 1 3属 ( 1 8.3% )。主要属为虾脊兰属、羊耳蒜属、玉凤花属、石斛属、兰属、石豆兰属 ,其中 2属为世界分布属 ,2属为热带分布属 ,2属为热带—亚热带分布属。广东山区兰科植物区系的地理成分较为复杂、多样 ,以热带亚洲成分 (占 39.4 % )为主导成分 ,其次为热带亚洲至热带大洋洲分布成分 ( 1 6.9% )。广东山区没有特有属 ,但特有种丰富 ,产中国特有种 39种 (占 1 8.8% ) ,其中广东特有种 6种 (占 2 .9% )。广东山区具有兰科植物从最原始到最进化各类型的代表。区系成份比较表明 ,本区与云南、广西和中南半岛兰科植物区系有较密切的联系。结果表明本区兰科植物区系的古老原始性 ;具有从热带向亚热带过渡的特点 ;与热带亚洲兰科植物区系具有密切的关系 ;可能是中国兰科植物演化中心的一部分。     

长江中游(以湖北湖南为主)的植物生物多样性及其保护对策

在对植物调查研究的基础上,对长江中游(湖北、湖南为主)的植物区系、植被、生物多样性保护及保护对策进行了系统的论述。根据两省土著种子植物名录统计,本区共有202科1476属7037种(包括种下等级),其中裸子植物7科30属64种;被子植物196科1445属6973种。以鄂湘为代表的华中区分布类型复杂、物种丰富、起源古老,而且特有的科、属、种多,特有度高。北温带木本植物属高度集中,体现了长江中游具有古第三纪．泛北极植物区系的代表性。拥有众多的东亚特有属、东亚．北美间断分布属和中国特有属,它们既是本地植物区系的特色,也代表了中国植物区系的核心。本地中山以亮叶水青冈(Fagus lucida)为主的阔叶林系第三纪．泛北中生落叶阔叶林的后裔。在植被区划上,本区属于常绿阔叶林区域,包括北亚热带常绿阔叶．落叶阔叶混交林地带及中亚热带常绿阔叶林两个植被地带。后者分为北部典型常绿阔叶林亚地带,南部含华南植物区系成分的常绿阔叶林亚地带。本区主要的自然植被类型(以原生类型为主)有171个类型(相当于群系formations)。从生物多样性保护的三个层次上(物种、群落、景观)对保护现状、特点、保护方针和策略等进行了探讨并提出了建议。     

高黎贡山兰花的多样性

对高黎贡山兰科植物的生物地理学和多样性进行了研究。1.兰科是高黎贡山种子植物中最大的科,包括75属265种。2.高黎贡山兰花起源于新、旧世界的热带和温带, 热带属占60%(45属),温带属占38.67%(29属),包括2个云南特有属。但是,高黎贡山兰科植物与地中海地区和中亚地区的联系十分微弱。3.高黎贡山的兰花以地生兰为主。这里,57.33%(43属)为地生兰,而附生兰和腐生兰仅分别为31属和3属。4.兰花物种的分布区式样表明高黎贡山兰花以温带兰为主 温带兰占总种数的69.43%(184种),包括东亚成分即滇西高黎贡山-东喜马拉雅分布的种和中国西南部特有种,它们是高黎贡山兰花区系的核心。5.高黎贡山兰科的特有现象在于1)具有云南二个特有属蜂腰兰Bulleyia和反唇兰Smithorchis;2)有高黎贡山特有种21个,如泸水兜兰Paphiopedilum markianum,贡山风兰Cymbidium gongshanense,贡山贝母兰Coelogyne gongshanense,热带附生兰——万带兰亚科在高黎贡山没有形成特有种;3)高黎贡山北段的特有种比南段丰富贡山有14种,腾冲仅有4种; 海拔1800～2100 m的梯度带特有种最多(13种);4)高黎贡山有云南特有种10种,其中小花槽舌兰Holcoglossum junceum是一个热带种,因为板块位移而来到了亚热带地域;5)高黎贡山的兰科植物中有19.25%(51种)是中国特有种,它们出现在高黎贡山,分布在云南其他地区和西南的一些省区。高黎贡山特有种,分布到高黎贡山的云南特有种和分布到高黎贡山的中国特有种一共为82种,占高黎贡山兰科总种数的30.91%, 兰科在高黎贡山是一个特有化程度很高的类群。     

江西木兰科植物区系地理分析

对江西木兰科植物7属23种的地理分布和区系特征进行了分析。属的分布区类型可划分为：热带亚洲分布、东亚一北美间断分布和中国特有分布。种的分布区类型可划分为：热带亚洲分布、东亚分布和中国特有分布。江西木兰科植物可划分为赣北、赣西北、赣西南、赣南、赣东南、赣东北共6个分布区。该区系以亚热带成分为主,具有种类丰富、区系成分复杂、多型性突出、特有现象较显著和与周边省份联系较密切等特点,属木兰科植物现代分布中心边缘分化比较强烈的区域之一。     

广西苦苣苔科植物区系和生态特点研究

滇黔桂及其邻近地区是我国苦苣苔科植物的分布和特有中心 ,广西正处于这个中心的位置上 ,种类十分丰富 ,共计有 38属、 16 6种 (含种下等级 ,下同 ) ,属和种的分布区类型不太复杂 ,特有现象极为突出 ,其中仅产广西的特有属有 5个 ,特有种达 81个。广西苦苣苔科植物区系与相邻的贵州、云南两省属的相似性系数较高 ,分别为 75 76 %和 71 4 2 % ,但与相邻省份苦苣苔科植物种的相似性系数却较低 ,从 35 4 8%至 6 4 9%不等。苦苣苔科植物在广西全境分布较广泛 ,但各地种类分布很不均衡。广西苦苣苔科植物的天然分布对基质有较严格的专一性 ,种群植株数量一般较少 ,同一种类不同的居群间形态变异较大。     

癞蝗科（Pamphagidae）在中国的分布和演化

癞蝗科在中国共有２个亚科,即分布在中国西北部的蠢蝗亚科Ｔｈｒｉｎｃｈｉｎａｅ和东北部的癞蝗亚科Ｐａｍｐｈａｇｉｎａｅ,这种分布格局很可能是由于青藏高原隆起后使中亚气候变得干旱少雨才形成的。在癞蝗科的１２个属、４２个种中（蠢蝗亚科１１属４０种,癞蝗亚科１属２种）,特有成分占有绝对优势,计有特有属６个、亚特有属３个、特有种３３种,这些特有成分的分布范围均很狭小,基本分布在以贺兰山为中心的荒漠、半荒漠草原中。蠢蝗亚科的特有成分很可能均起源于波腿蝗属ＡｓｉｏｔｍｅｔｈｉｓＵｖ．或者它们来源于共同的祖先。     

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