A Study on the Genus Chrysosplenium L. from China (Cont.)

This paper deals with the taxonomy and geographic distribution of the genus Chrysosplenium L. in China. Based on the characters and evolution of the seed, capsule, disk, ovary and leaf, the species of this genus can be grouped into 2 subgenera, 5 sections and 16 series. There are 2 subgenera, 5 sections and 11 series in China. They are as follows: I. Subgen. Gamosplenium Maxim. emend. J. T. Pan Leaves alternate. Lectotype: Chrysosplenium carnosum Hook. f. et Thoms. 1. Sect. Alternifolia Franch. emend. J. T. Pan Seeds smooth and glabrous. Type: Chrysosplenium alternifolium L. (1) Ser. Nudicaulia Maxim. emend. J. T. Pan Disk obscure or absent; ovary nearly half-inferior, sometimes mostly inferior; capsule generally subtruncate and emarginate at top and bilobed with equal and horizontally divaricate or suberect lobes; seeds smooth and glabrous. Type: Chrysosplenium nudicaule Maxim. (2) Ser. Alternifolia Maxim. emend. J. T. Pan Disk 8-lobed; ovary nearly half-inferior; capsule generally subtruncate and emarginate at top, and bilobed with equal and horizontally divaricate lobes; seeds smooth and glabrous. Type: Chrysosplenium alternifolia L. 2. Sect. Nephrophylloides Turcz. Seeds minutely papillose or pilose. Type: Chrysosplenium sedakowii Turcz. (1) Ser. Macrophylla Franch. emend. J. T. Pan Disk obscure or absent; ovary nearly half-inferior; capsule nearly truncate and emarginate at top, and bilobed with equal lobes; seeds minutely papillose. Type: Chrysosplenium macrophyllum Oliv. (2) Ser. Ovalifolia Maxim. emend. J. T. Pan Disk generally 8-, rarely 4-, lobed, papillae absent around disk; ovary mostly inferior; capsule subtruncate and emarginate at top; seeds minutely papillose or pilose. Type: Chrysosplenium ovalifolium M. Bieb. ex Bunge (3) Ser. Lanuginosa Hara, emend. J. T. Pan Papillae numerous, brown around reduced disk; ovary mostly inferior; capsule nearly truncate and emarginate at top; seeds minutely papillose. Type: Chrysosplenium lanuginosum Hook. f. et Thoms. II. Subgen. Chrysosplenium Leaves opposite. Type: Chrysosplenium oppositifolium L. 1. Sect. Trichosperma J. T. Pan, sect. nov. Capsule not truncate at top, and bilobed with subequal, suberect or divergent lobes. Type: Chrysosplenium trichospermum Edgew. ex Hook. f. et Thoms. This section is divided into 4 series in the world, with only 1 in China. (1) Ser. Nepalensia Maxim. emend. J. T. Pan Disk obscure or absent; ovary generally mostly inferior; cassule not truncate at top, and bilobed with subequal and suberect or divergent lobes; seeds smooth and glabrous. Type: Chrysosplenium nepalense D. Don 2. Sect. Grayana J. T. Pan, sect. nov. Capsule bilobed with distinctly unequal and ascending lobes. Type: Chrysosplenium grayanum Maxim. This section consists of 4 series in the world, with 3 series in China. (1) Ser. Sinica Maxim. emend. J. T. Pan Disk obscure or absent; ovary nearly half-superior; capsule bilobed with distinctly unequal and ascending lobes; seeds minutely papillose. Type: Chrysosplenium sinicum Maxim. (2) Ser. Esulcata Franch. emend. J. T. Pan Disk (4)-8-lobed; ovary generally half-inferior; capsule bilobed with unequal and ascending lobes; seeds minutely papillose or pilose. Lectotype: Chrysosplenium dubium J. Gayex DC. (3) Ser. pilosa maxim. emend. J. T. Pan Disk obscure or absent; ovary nearly half-inferior; capsule bilobed with distinctly unequal and ascending lobes; seeds distinctly longitudinally ll-18-costate and minutely papillose or tuberculate on the ridge. Type: Chrysosplenium pilosum Maxim. 3. Sect. Chrysosplenium Capsule nearly truncate and emarginate at top, and bilobed with equal and horizontally divaricate lobes. Type: Chrysosplenium oppositifolium L. (1) Ser. Romosa J. T. Pan, ser. nov. Disk distinctly 8-lobed, papillae sparse, brown around disk; ovary mostly inferior; capsule nearly truncate and emarginate at top, and bilobed with equal and horizontally divaricate lobes; seeds smooth and glabrous. Type: Chrysosplenium ramosum Maxim. This series is monospecific one, also occurring in China, namely C. ramosum Maxim. (2) Ser. Delavayi Hara Disk distinctly 8-lobed, Papillae sparse, brown around the disk; ovary mostly inferior; capsule nearly truncate and emarginate at top, and bilobed with equal and horizontally divaricate lobes; seeds distinctly longitudinally 10-16-costate and transversely striate on the ridge. Type: Chrysosplenium delavayi Franch. This series can be considered as the most advanced one in the Chrysaspleninm L. So far, the Chrysosplenium L. comprises 64 species in the world, among which 1 species is found in North Africa, 2 in South America, 4 in Europe, 5 in North America, 56 in Asia, of which 3 occur in Sikkim, 5 Bhutan, 5 Mongolia, 6 north Burma, 6 Korea, 7 north India, 8 Nepal, 12 Japan, 17 U.S.S.R. (of which 3 also in Europe), 34 China (including 22 endemic species and 3 new species). In China, Fujian and Guangdong Provinces and Zhuang Autonomous Region of Guangxi each has only 1 species, Taiwan, Zhejiang, Shanxi and Hebei Provinces and Uygur Autonomous Region of Xinjiang each has 2, Anhui, Jiangxi and Hunan Provinces each has 3, Qinghai Province 4, Heilongjiang, Liaoning and Guizhou Provinces each has 5, Jilin and Hubei Provinces each has 6, Gausu Province 8, Shaanxi Province and Xizang (Tibet) Autonomous Region each has 10, Yunnan Province has 11, Sichuan Province has 14. Thus the distribution centre of this genus should be in the north temperate zone of Asia, and the region covering Shaanxi Gansu, Sichuan, Yunnan and Xizang may be regarded as an important part of this centre. The 7 species of Ser. Nudicaula Maxim. emend. J. T. Pan can be considered as the most primitive ones in this genus. They are mostly distributed in Shaanxi (Qin Ling), south Gansu, southeast Qinghai, southwest Sichuan and nothwest Yunnan of China. This region may be considered as the centre of the origin (or at least differentiation) of this genus. The new species and the new varieties described in this paper are as follows: C. hydrocotylifolium Levl. et Vant. var. emeiense J. T. Pan, C. taibaishanense J. T. Pan, C. lixianense Jien ex J. T. Pan, C. qinlingense Jien ex J. T. Pan.     

中国虎耳草属(虎耳草科)二新种————班玛虎耳草和丁青虎耳草

记载了中国虎耳草属Saxifraga二新种, 即班玛虎耳草S. banmaensis J. T. Pan和丁青虎耳草S. dingqingensis J. T. Pan。其中, 班玛虎耳草仅见于青海班玛, 与小伞虎耳草S. umbellulata Hook. f. &; Thoms.近缘, 但其萼片先端具软骨质短尖头, 花瓣线形, 非提琴状长圆形至提琴形, 基部无爪, 可资区别。丁青虎耳草见于西藏丁青, 与近加拉虎耳草S. llonakhensis W. W. Smith相似, 但其萼片3脉, 于先端汇合成1疣点, 花瓣具8痂体和4-5脉, 基部截形或近耳形, 可以区别。此两种均系中国特有种, 隶属于莲座状亚组subsect. Rosulares Gornall。     

横断山岩白菜属新分类群

天全岩白菜 新种 图1 Bergenia tianquanensis J. T. Pan, sp. nov. Species inter B. emeiensem C. Y. Wu et B. stracheyi (Hook. f. et Thoms.) Engl.media; sed differt a priore laminis foliorum dentatis necnon serratis, margine pro infimaparte ciliatis, petiolis supra ochream pilosis, scapo glanduloso-piloso; a postriore laminis fo-liorum margine a medio ad superam partem glabris, sepalis margine glabris, nervis sepalo-     

Cladistics and Biogeography of Artemisia sect. Viscidipubes and sect. Albiraotea (Compositae)

Twenty-six species and eight varieties of Sect．Viscidipubes & Sect．Albibractea are endemic to Asia．Most species of Sect．Viscidipubes are distributed from low to high altitudes and cold areas in the Hengduan-Himalayan Mountains,with only a few species extending to E or S Asia．Sect．Albibractea is distributed mainly in the subtropics and tropics,lower altitudes and moist areas in S & SE Asia,with a few species extending to the Qinling range of China．Both sections are more advanced than the other sections．They were studied by cladistic analysis and outgroup comparison．Data matrix of 55 characters from stems,leaves,inflorescences,female flowers,bisexual flowers,achenes,pollen grains and chemical constitution was employed in separate and combined studies．Eighteen most parsimonious cladograms were generated with 358 steps,consistency index of 0．72 and retention index of 0．87． 1．Within Artemisia,Sect．Viscidipubes and Sect．Albibractea are sister groups to all the other groups． 2．We support the idea to separate Sect．Viscidipubes (incl．Ser．Viscidipubes,Ser．Erlangshanenses and Ser. Pleiocephalea) and Sect．Albibractea (incl．Ser．Albibractea,Ser．Flaccidae and Ser. Anomalae)．The authors suggest that Ser．Anomalae include A．deversa and Ser．Erlangshanenses include A．zayuensis and A．yadongensis as well as Ser．Viscidipubes include A．gyitangensis and A．boreali-siamensis．As the result of the cladistic analysis,the authors tend to propose a new series, Ser．Tanguticae,incl．A．tangutica in the section． 3．We consider that SW China,especially W Sichuan,is the speciation center and the tration of the present distribution center．4．A．boreali-siamensis,only in N Thailand,is not related to the widely distributed species in Ser．Pleiocephalae,such as A．atrovirens,A．chingii and A．myriantha,but rather closely related to species,such as A．vexans,A．occidentali-sichuanensis,which are endemic to W.Sichuan and E．Xizang．     

Notulae de Gesneriaceie Sinensibus (IX)

Ten new species, three new varieties and a new section of the family Gesneriaceae are described from China in the present paper. They are Tremacron urceolatum K. Y. Pan from Muli of SW Sichuan, T. obliquifolium K. Y. Pan from Miyi and Yanyuan of SW Sichuan, T. aurantiacum K. Y. Pan from Mabian and Pinshan of S Sichuan, lsometrum Sect. Chorianthera W. T. Wang et K. Y. Pan (with I. eximium Chun as the section type), Isometrum eximium Chun ex K. Y. Pan from Jiulong, Muli and Jinyang of SW Sichuan; Ancylostemon mairei (Levl.) Craib var. emeiensis K. Y. Pan from Mt. Emei of Sichuan, A. aureus (Franch.) Burtt var. angustifolius K. Y. Pan from Zhenkang of SW Yunnan, A. gamosepalus K. Y. Pan from Hanyuan, Yanyuan and Yuexi of SW Sichuan, A. rhombifolius K. Y. Pan from Meigu of SW Sichuan, A. ronganensis K. Y. Pan from Rong an of Guangxi; Corallodiscus flabellatus) (Craib) Burtt var. puberulus K.Y. Pan from Zhongdian and Deqin of NW Yunnan, Nanchuan of S Sichuan and Zayü of Xizang (Tibet), Beccarinda minima K. Y. Pan from Jinxiu and Xiangzhou of Guangxi, Boeica stolonifera K. Y. Pan from Fangcheng, Shiwandashan, Pingnan and Dongxing of S Guangxi, B. multinervia K. Y. Pan from Yingjiang of W Yunnan, and Paraboea barbatipes K. Y. Pan from Napo of W Guangxi and Xichou of SE Yunnan.     

中国-喜玛拉雅特有属——蓝钟花属的分类修订

Cyananthus Wallich ex Bentham, the only genus of Campanulaceae with superior ovary, is revised to clarify infrageneric relationships and phylogeny of the genus. Evidence obtained from the comparative gross morphology, anatomy, palynology, and karyomorpho-logy recommends a new infrageneric classification of the genus, recognizing 23 species, belonging to two subgenera, four sections and four subsections. One subgenus(Subgen. Mi-cranthus), one section(Sect. Suffruticulosi) and two subsections(Subsect. Flavi and Sub-sect. Lichiangenses)are described as new taxa. New combinations at sectional (Sect. Annui) and subsectional(Subsect. Stenolobi) ranks are also proposed. The genus Cyananthus is strictly distributed in the high mountains of China(Xizang, Yunnan and Sichuan), extending to Bhutan, Nepal and India (Kumaon-Garhwal, Assam and Sikkim), with altitudinal ranges from 2500 ~ 5300 m. It is observed that 13 species are endemic to SW China and only three species are endemic to the Himalayas( two species in Ne     

A Revision of Genus Yinshania (Cruciferae)

The genus Yinshania was established by Ma Yu-chuan and Zhao Yi-zhi in 1979, when only one species, Y. albiflora Ma et Y. Z. Zhao, was discribed from Nei Monggol. In the present paper the genus Yinshania is revised and four new species, two new varieties and four new combinetions are reported. There are so far eight species and two varieties in total in this genus. Important morphological characters of the genus are analysed, which shows that the lateral nectariferous glands positioned at lateral base of the brevistamens are triangularovoid; there are dense minute pustules on the surface of valves, which is easily neglected because the pustules disappear or shrinked when dry; simple or furcate hairs are present in the most species, seldom absent; the shape of pollen grains is relatively steady, elliptic or long-elliptic, with the polar view trifidcircular, the equatorial view elliptic or long elliptic, the aperture 3-colpate, exine reticular. The type of genus Yinshania is changed. Cochlearia acutangula O. E. Schulz was published in 1929, but Y. albiflora Ma et Y. Z. Zhao in 1979. They are the same species and a new combinetion, Y. acutangula (O. E. Schulz) Y. H. Zhang, is made. Thus, the type of genus Yinshania should be changed to Y. acutangula (O. E. Schulz) Y. H. Zhang. Besides, He Ye-qi 6121 (paratype, PE), which is different from Y. acutangula var. albiflora, is separated from it and transferred the typical variety, Y. acutangula. According to the characters of fruit shape the genus Yinshania is divided into two sections, namely, Sect. Microcarpa and Sect. Yinshania, and then Sect. Yinshania is subdivided into two series. Sect. 1. Microcarpa. Silicles widely ovoid or subglobose, 1-2.2 mm long, 0.8-2.2 mm wide, the ratio of length and width about 1.1. Sect. 2. Yinshania. Silicles oblong, oblong-ovoid or long-lanceolate, ellipsoidal, 1.5-4.5 mm long, 0.3-1.5 mm wide, the ratio of length and width about 2.5-3.3. Ser. 1. Henryanae. Raches flexuose; plants densely hairy; leaves 3-5-foliolate, seldom pinnatipartite or pinnatisect. Ser. 2. Yinshania. Raches non flexuose; plants sparsely hairy; leaves pinnatisect or pinnatipartite. The genus Yinshania is a genus endemic to China, with their range from eastern Xizang to western Hubei from northern Guizhou to central Nei Monggol. The taxa are mostly of a small area. Sect. Microcarpa is concentrated in Sichuan and southern Gansu; Sect. Yinshania is spread from Xizang and Sichuan, nouthwards to Gansu, Ningxia, Shanxi, Hebei and Nei Monggol (Ser. Yinshania); and from Sichuan south-eastwards to Guizhou and Hebei (Ser. Henryanae). There are five species in Sichuan. The present paper conjectures that the distribution centre of the genus is in the Hengduan Mountains and its adjacent areas.     

Notulae De Ranunculaceis Sinensibus(ⅩⅩⅡ)

(1) In the overwhelming majority of genera of the family Ranunculaceae, includ ing its primitive genera, Caltha, Calathodes, and Trollius and the primitive genus of trib. Anemoneae, Anemone, the sepals are spreading and the stamens are glabrous. So, the as cending or upright sepals and hairy stamens of the sections Meclatis, Tubulosa, Viorna, and Atragene of the genus Clematis are secondary, and are accordingly considered as advanced characters, and those sections and the genus Archiclematis, closely related to Sect. Viorna Subsect. Connatae, more or less advanced groups. (2) In the sections Cheiropsis, Fruticella, and Viticella, which have glabrous stamens,some species have spreading sepals, and the others have ascending or upright sepals. In Sect. Clematis, all the species have spreading sepals and glabrous stamens, except for Clematis pinnata, which has ascending sepals and usually hairy stamen filaments. In Sect. Lasiantha with 2 species restricted to western U. S. A., C. lasiantha has glabrous stamens, while C. paucifiora has stamens hairy on fliaments. In Sect. Naraveliopsis with spreading sepals,the majority of species have glabrous stamens, but one species, C.liboensis, endemic to Guizhou Province, China, has hairy stamens. These facts just mentioned indicate that the evolution of sepals and stamens took place in several lineages independently in Clematis. (3) In Clematis, glabrous stamens of C.apiifolia, C.grata, and C.montana with linear filaments and oblong anthers, are similar to those of Caltha, Calathodes, Trollius, and Anemone. Thus, the linear filaments and oblong anthers are considered primitive characters in Clematis. On the other hand, lanceolatelinear filaments of C. tangutica and C. aethusifolia or oblanceolate -linear filaments of C. courtoisii and C. loureiriana and linear anthers of C. meyeniana and C. uncinata, and narrow-linear anthers of C. courtoisii and C. lanuginosa are considered advanced ones. In ease of stamens with hairs, stamens of C. henryi with densely villous filaments and those of C. kweichowensis with both filaments and anthers densely pubescent show more advanced condition than those of C. pinnata, C. heracleifolia, and C. tangutica, with sparsely puberulous filaments and glabrous antbers(Fig. 1 ). (4)The pedunculate, 2-bracteate dichasial cyme with several flowers may represent the primitive type of inflorescences in Clematis. Manyflowered panicle-like cymes as in C.gouriana and C. tsaii, or few-l-flowered cymes as in C. henryi and C. repens, and cymes lacking peduncles and bracts as in C. montana and C. pogonandra are all considered advanced. Besides, the fact that flowers arise from axillary buds of old branches shows also an advanced condition. (5)Sect. Clematis subsect. Pinnatae, with leaflets, inflorescence ramification, and stamens similar to those of C. heracleifolia, is considered intermediate between Sect. Clematis and Sect. Tubulosa. (6) Subsect. Clematis and Subsect. Rectae, and Subsect. Connatae and Subsect. Crispae are so closely related to each other respectively that it is difficult to ascertain the systematic position of some intermediate species between the two subsections of each pair in the absence of seedlings. So, in the present paper, following the classification of Clematis proposed by Tamura in 1967, I put Subsect. Clematis and Subsect. Rectae in Sect. Clematis, and Subsect. Connatae and Subsect. Crispae in Sect. Viorna. (7)According to the evolutionary tendencies mentioned above, a realignment of the sections and the infrasectional taxa of the Chinese Clematis is made. (8) Six subsections, 6 serise, 2 species, and 4 varieties are described as new, and 5 new combinations, 4 new ranks, and 2 new names are given. (9)The specific rank of C. tenuipes W.T. Wang, reduced to varietal renk in 1980, is restord. C. taiwaniana Hayata, reduced to synonomy of C. grata Wall. in 1991, is considered distinct from the latter in hairy adaxial surface of sepal and narrower achene with tapering apex. C. kerriana Drumm. & Craib and C. laxipaniculata Pei are proved to be conspecific to C. subumbellata Kurz and reduced to syn-onymy.     

A Cytotaxonomic Study on Chinese Dioscorea L.—The Chromosome Numbers and Their Relation to the Origin and Evolution of the Genus

The chromosome numbers of 5 tuberous sections of Chinese Dioscorea, including 23 species and varieties, are reported in the present paper as a continuation of the previous reports. They are all polyploids with the basic number x=10. On the basis of analysis of chromosome numbers of whole genus, the rhizomatous diploid species of Sect. Stenophora Uline are presumed to be primitive taxa, while the polyploids of chromosome numbers 40-142 are considered derived groups as a result of hybridization between their ancestral diploids followed by chromosome doubling. Sect. Lasiophyton Pr. et Burk., Sect. Opsophyton UIine, Sect. Shannicorea Pr. et Burk., Sect. Combilium Pr. et Burk. and Sect. EnantiophylIum Uline may be the advanced groups. The chromosomal evolution and geographical distribution suggest that the primitivediploid might have originated in Hengduan Mountains of Asia, an old highland.     

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.     

唐松草属六新种

描述了毛茛科唐松草属六新种:(1)大关唐松草,发现自云南东北部,与多枝唐松草甚为近缘,区别为其小叶较厚,较大,多呈卵形或宽卵形,心皮花柱较短,稍向后弯曲,瘦果呈新月形。(2)宽柱唐松草,发现自甘肃南部,其特征为心皮花柱扁平,近长圆形,腹面无柱头或柱头组织,据此特征可与此属中国其他种区别。(3)六脉萼唐松草,发现自四川中部,与白茎唐松草近缘,区别为其茎和小叶有毛,萼片具六条脉,一些雄蕊的花药败育,子房被短柔毛,柱头无翅。(4)吉隆唐松草,发现自西藏南部,与白茎唐松草甚为近缘,区别为小托叶卵形、急尖,复单歧聚伞花序一条顶生,无侧生者,雄蕊花药呈狭长圆形,顶端钝,无短尖头。(5)螺柱唐松草,发现自云南西北部,可能与白茎唐松草有亲缘关系,区别为其萼片具1条脉,花有4~5枚雄蕊,心皮花柱顶部螺旋状弯曲,柱头不明显。(6)札达唐松草,发现自西藏西南部,与多叶唐松草近缘,区别为其小叶顶端急尖,边缘具尖牙齿,聚伞圆锥花序具少数分枝和少数花,萼片狭卵形,花药狭长圆形。     

青藏高原跳甲亚科昆虫区系研究

讨论青藏高原（包括横断山区）的跳甲亚科昆虫区系。该区已知47属228种。1）据属级阶元的分布类型分析,以东洋属和南型属种显占优势,是区系主体,显示该区跳甲区系的热带渊源,其中高山属种赋予该区以高山区系特征;2）该区物种分化活跃,是某些多种属中国种类的分布中心和分化中心;3）联系中国跳甲亚科区系,在地理分布格局上显示西－东分布,如Hespera属的分布和西南－东北分布或西南－东北的间断分布格局,如Pentamesa和Stenoluperus属的分布。这种地理分布格局反映青藏高原的隆起给中国昆虫区系带来重要影响。     

椴树属的地理分布

椴树属Tilia是椴树科一个形态特殊且唯一的北温带分布属,分布于亚洲、欧洲和北美,构成典型的北温带分布格局,三个分离的分布区之间缺乏共有种。本文对各分布区的种类进行重新评价,确认全属25种。其中东亚17种,占68％,包含了现存种类各个演化阶段的类群,是现代分布中心;欧洲-西西伯利亚6种,属于木果组及壳果组;北美2种,均为木果组成员。化石分布与现代地理分布格局基本相似,但分布纬度较现代分布偏北,达到北纬80°附近,且还出现于现今无椴树分布的亚洲大陆腹地,北美西部椴树至第三纪末完全绝迹,而东部到第四纪才有化石记录。根据现代地理分布,结合化石证据、地质历史、气候变迁及形态演化推测,椴树属可能在白垩纪晚期起源于中国东部亚热带山地,至少到始新世之前已散布至欧洲和北美西部。渐新世之后的全球降温和更新世大冰期对椴树属现代地理分布格局的形成起着至关重要的作用。     

A Study on the Genus Saxifraga L. from China

This paper presents a system of the genus Saxifraga L. from China, recognizes 2 subgenera, 8 sections, 7 subsections (including 1 new subsection), 31 series (including 23 new series), 4 subseries (new subseries) and 203 species (including 2 new species and 4 new varieties). The new taxa, statuses, combinations and names in this paper are as follows: Sect. Biro- stres (Gornall) C. Y. Wu et J. T. Pan, stat. nov.,; Sect. Punctatae (Engl.) J. T. Pan, stat. nov.; Ser. Rufescentes J. T. Pan, ser. nov.; Saxifraga lonshengensis J. T. Pan, sp. nov.; S. rufescens Balf. f. var. uninervata J. T. Pan, var. nov.; S. rufescens Balf. f. var. flabellifolia C. Y. Wu et J. T. Pan, nom. nov.; Ser. Stonoliferae J. T. Pan, ser. nov.; Ser. Stellariifoliae (Engl. et Irmsch.) J. T. Pan, stat. nov.; Subser. Aristulatae J. T. Pan, subser. nov.; Subser. Montanae J. T. Pan, subser, nov.; Saxifraga ciliatopetata (Engl. et Irmsch.) J. T. Pan var. ciliata J. T. Pan, var. nov.; Subser. Gonggashanenses J. T. Pan, subser, nov.; Subser. Car- diophyllae J. T. Pan, subser. nov.; Saxifraga egregia Engl. var. xiaojinensis J. T. Pan, var. nov.; Ser. Caveanae J. T. Pan, ser. nov.; Ser. Heterocladoideae J. T. Pan, ser. nov.; Ser. Chumbienses J. T. Pan, ser. nov.; Ser. Bulleyanae J. T. Pan, ser. nov.; Ser. Brachypodae C. Y. Wu et J. T. Pan, ser. nov.; Ser. Erinaceae J. T. Pan, ser. nov.; Saxifraga substrigosa J. T. Pan var. gemmifera J. T. Pan, var. nov.; Ser. Umbellulatae J. T. Pan, ser. nov; Ser. Yu- shuenses J. T. Pan, ser. nov.; Ser. Ungviculatae J. T. Pan, Ser. nov.; Ser. Punctu- latae J. T. Pan, ser. nov.; Ser. Candelabriformes J. T. Pan, ser. nov.; Ser. Tanguti- cae J. T. Pan, ser. nov.; Saxifraga tangutica Engl. var. platyphylla (H. Smith) J. T. Pan, comb. nov.; Ser. Yaluzangbuenses J. T. Pan, ser. nov.; Ser. Jainzhuglaenses J. T. Pan, ser. nov.; Saxifraga jainzhulaensis J. T. Pan, sp. nov.; Ser. Jacquemontianae J. T. Pan, ser. nov.; Ser. Nanae J. T. Pan, ser. nov.; Subsect. Microgynae J. T. Pan, subsect. nov.; Ser. Nangxi- anenses J. T. Pan, ser. nov.; Ser. Mucronulatae J. T. Pan, ser. nov.; Ser. Parkaenses J.T. Pan, ser. nov.; Ser. Deqenenses J. T. Pan, ser. nov.; Saxifraga mucronulatoides J. T. Pan, nom. nov.     

A Study on Dichocarpum (Ranunculaceae)

The genus Dichocarpum was established by W. T. Wang and Hsiao in 1964, who divided the genus into 2 sections: Sect. Dichocarpum including 10 species distributed on the mainland of E. Asia, and Sect. Hutchinsonia including 9 species native to Japan. M. Tamura and L. A. Lauener made a revision of the genus in 1968, who divided the genus into 4 sections, three for the species of the mainland of E. Asia, including 3 series and 10 species, and the other for the species of Japan, including 2 subsections, 3 series and 9 species. In the present paper, the genus is divided into 2 sections and 6 series, including 15 species and 3 varieties, and a putative phylogeny of the genus is proposed. The genus may be close to the genus Asteropyrum, and these two genera are rather specialized in Thalictroides (Ranunculaceae), because they have three very similar characters: the petal with a long claw, the stephanocolpate pollen and the chromosome morphology. The genus has 2n=24, 35(36?), which indicates that its basic number is X=6, and the species on the mainland of E. Asia (Sect. Dichocarpum) may well be paleotetraploids, whereas those in Japan (sect. Hutchinsonia) are paleohexaploids. Most of the advanced species are distributed in Japan and the most primitive ones in China and the Himalayas, the distribution pattern seggests that the Japanese members of this genus might have immigrated from China in the Tertiary, and differentiated and evolved there. The putative phylogeny of the genus is shown in Fig. 2 (at series level)     

论世界蒿属植物区系

本文从多学科, 包括形态、地理分布、孢粉、古植物、谱系分支分析及化学成分等学科的研究, 论述了世界蒿属植物的系统分类及其种属地理、历史地理和区系地理.     

The Classification and Distribution of the Genus Calligonum L. in China

The genus Calligonum L. includes a total number of 35 species in the world, of which 24 are in China. They are grouped into four sections, of which Sect. Calliphysae (Fisch. et Mey.) Borszcz. is the most primitive and Sect. Medusae Sosk. et Alexender. is the most progressive. The Calligonum L. is an ancient genus in the arid desert flora, and central Asia is the place of its origin. Some species migrated to the Middle Asia and Iran, developing into a second center there. Also, some newly occurred species of the Middle Asia emigrated eastwards to central Asia, so the genus Calligonum L. in China comprises components of both central Asia and the Middle Asia. The genus Calligonum L. is distributed in North Africa, south Europa and Asia, and China is the eastmost part of the distribution range. They grow in Nei Monggol, Gansu, Qinghai and Xinjiang. There are 12 species in the Zhuengar Basin, covering 50 percent of the total number of species in China, amd thus the genus is the most abundant there.     

572. BERGENIA EMEIENSIS

Summary.  Bergenia emeiensis C.Y. Wu ex J.T. Pan is illustrated and described. Its relationship to other Himalayan species is discussed, and instructions for its cultivation are given.     

The Origin,Evolution and Distribution of Ligularia Cass. (Compositae)

The genus Ligularia Cass. is one of the large genera in Compositae-SenecioneaeTussilagininae. In subtrib. Tussilaginae, Ligularia is closely related to, but more advanced than, the genus Farfugium Lindl. It includes six sections, 11 series and 129 species. All the taxa are distributed in Asia with only two species extending to Europe. There are 119 species in E. Asia, Comprising 96 % of the world total. The highest concentration of species in E. Asia occurs in the Hengduan Mountains. In this area there are four section, six series and 67 species, of which 61 species are local endemics; thus 66% of sections, 54.5% of series and about 52 % of species in the world occur in this small area, indicating that it is a major distribution centre for Ligularia. According to character analysis, sect. Corymbosae ser. Calthifoliae with 5 species was considered as the most primitive group in this genus, which has reniform leaves, palmate veins, a few large capitula (arranging in Corymb-like inflorescence), and semispherical involucre etc. The primitive species, L. dentata and L. hodgsonii, are distributed from E. Sichuan to Japan via Hubei, Hunnan, Anhui, Fujian. This distribution pattern is consistent with that of its allied genus, Farfugium. According to the principle of common origin, the ancestors of the two genera appeared most probably in the same area. It was inferred that the area from E. Sichuan of China to Japan was the original area of the genus Ligularia, However, on the basis of geological history and the modern distribution of this genus, the author considers that central China with E. Sichuan might be the primary original area of Ligularia. Its dispersal route was mainly along the mountains of southern margin of Asia, with relatively few members dispersed northea stwards to NE. Asia. The origi-nal time of the genus Ligularia was at least not later than the middle Cretaceous.