鳞毛蕨科四个属的染色体数目

报道了鳞毛蕨科的4个属(毛枝蕨属Leptorumohra、石盖蕨属Lithostegia、黔蕨属Phanerophlebiopsis和柳叶蕨属Cyrtogonellum)6种植物的染色体数目及生殖方式。其中柳叶蕨Cyrtogonellum fraxinellum 'n'=123, 2n=123; 离脉柳叶蕨C. caducum 'n'=123; 斜基柳叶蕨C. inaequalis 2n=123; 四回毛枝蕨Leptorumohra quadripinnata n=41; 石盖蕨Lithostegia foeniculacea 2n=164; 长叶黔蕨Phanerophlebiopsis neopodophylla 2n=82。石盖蕨属、黔蕨属和柳叶蕨属的染色体数目为首次报道。结果表明这3个属的染色体基数和鳞毛蕨科中其他属一样均为x=41。细胞学证据支持将石盖蕨属、黔蕨属置于鳞毛蕨科的处理。本文还发现柳叶蕨属与贯众属Cyrtomium的一些种一样, 具有无融合生殖方式, 而其他3个属仅具有在蕨类植物中较为常见的有性生殖方式。     

湖南鳞毛蕨属(鳞毛蕨科)一新种

描述了鳞毛蕨属一新种,即吉首鳞毛蕨Dryopteris jishouensis G.X.Chen et D.G.Zhang.吉首鳞毛蕨与稀羽鳞毛蕨Dryopteris sparsa(Buch.-Ham.ex D.Don)O.Ktze.相似,区别在于本新种形体较小,通常高5³6cm,羽片近对生或互生,裂片边缘全缘且顶端钝圆而无尖齿,囊群盖边缘啮蚀状.     

云南鳞毛蕨属纤维鳞毛蕨组的分类研究

本文记载云南产鳞毛蕨届纤维鳞毛蕨组植物16种,其中6种为云南新分布,1种为新改级。     

云南鳞毛蕨属植物分类概要

本文研究云南产鳞毛蕨属植物的属下分类并列出所有的种类。该属植物在云南现知至少有88种,属下可划分为3个亚属和12个组。为了使这些类群之间的特征轮廓清晰,本文提供了分亚属及分组的检索表。     

中国鳞毛蕨属泡鳞亚属的分类研究

鳞毛蕨属ＤｒｙｏｐｔｅｒｉｓＡｄａｎｓ．泡鳞亚属ＳｕｂｇｅｎｕｓＥｒｙｔｈｒｏｖａｒｉａｅ（Ｈ．Ｉｔｏ）Ｆｒａｓｅｒ－ＪｅｎｋｉｎｓｉｎＢｕｌ．Ｂｒ．Ｍｕｓ．Ｎａｔ．Ｈｉｓｔ．Ｂｏｔ．１４（３）：１９５．１９８６．Ｔｙｐｅ：Ｄｒｙｏｐｔｅｒｉｓｅｒｙ...     

贯众属10种植物染色体数目

对鳞毛蕨科Dryopteridaceae贯众属Cyrtomium Presl的10种植物的染色体数目进行报道。其中低头贯众C.nephrolepioides n=82,2n=164;单叶贯众C．hemionitis n=123,2n=c．123;惠水贯众C．grassum n=c．82,2n=164;披针贯众C．devexiscapulae 2n=164;小羽贯众C．lonchitoides 2n=82;大叶贯众C．macrophyllum 2n=164;云南贯众C．yunnanense n=123为首次报道。     

鳞毛蕨属一新组——金冠鳞毛蕨组

植株中等大小。根状茎直立或斜升。叶簇生。叶柄被金黄色披针形的鳞片。叶片一至二回羽状复叶。囊群盖大、贝壳状,革质,笼罩着成熟的孢子囊群。 本组与大果鳞毛蕨组Sect.Pandae Frasm-Jenkins接近,但叶片一至二回羽状,囊群盖贝壳状,故易区别。 该组大约有7种,云南产6种,本文记载5种。     

鳞毛蕨属一新组——高山鳞毛蕨组

<正> 植株成丛生长。根状茎直立或斜升,多分枝,具纤细的匍匐茎。叶簇生。叶柄被披针形棕色的鳞片。叶片卵状披针形,二回羽状。小羽片或裂片边缘有锯齿。囊群盖小,膜质。 该组近于sect. Fibrillosae Ching,但裂片的叶脉三分叉或羽状,容易区别;该组不同于sect. Dryopteris在于根状茎分枝。     

The genus Dryopteris in the Canary Islands and Azores and the description of two new tetraploid species

From studies in the field, botanic garden and herbarium we concluded that the following four species of Dryopteris grow on the Canary Islands: D. aemula (n = 41) so far found only on Gomera; D. pseudomas (n = 82, apogamous) similarly recorded only for Gomera; D. oligodonta (n = 41) the most common representative of the genus in the Islands is possibly an old Canary endemic related to some African species; D. guanchica a new tetraploid species ( n = 82) hitherto confused with D. austriaca (D. dilatata). On four islands of the Azores the following were found: D. aemula (n = 41); D. azorica (n = 41); D. pseudomas (n = 82, apogamous); and D. crispifolia a new tetraploid species ( n = 82) which is very distinct when living but in the dried pressed state is difficult to differentiate from D. austriaca and D. guanchica.     

国产十四种苋属植物的染色体数目

报道了国产14种苋属植物的染色体数目。部分种的染色体数目为2n=34,即反枝苋Amaranthus retroflexus,刺苋A．spinosus,红苋A．cruentus,腋花苋A．roxburghianus,合被苋A．polygonoides,皱果苋A． viridis,凹头苋A．lividus,苋A．tricolor。其他种的染色体数目为2n=32,即尾穗苋A．caudatus,绿穗苋A． hybridus,千穗谷A．hypochendriacus,繁穗苋A．paniculatus,北美苋A．blitoides,白苋A．albus。其中腋花 苋的染色体数目为首次报道。该属染色体基数为x=16,17。两种染色体基数在苋属2个组(sect．Ama- ranthus和sect．Blitopsis)中均存在。由于苋属植物染色体大多为小型染色体,因此对苋属植物目前尚不 能进行详尽的核型分析。     

A cytotaxonomic study of 10 species of the Polypodiaceae from Yunnan,China

A cytotaxonomic study was made of 10 fern species belonging to 7 genera of Polypodiaceae from Yunnan, China. Seven new records (including one cytotype) were reported in this paper. The putative reproduc-tive manners were inferred from cytological characters and spore counting. The chromosome numbers were 2n=70 in Polypodiastrum mengtzeense, Lepisorus bicolor; 2n=72 in Polypodiode amoena, P. wattii, L. mac-rosphaerus, Lepidogrammitis rostrata, Drymotaenium miyoshianum, Tricholepidium maculosum, Phymatopteris oxyloba; and 2n=108 in P. trisecta. The reproductive type in P. trisecta is triploid apogamous while it is of the sexual diploid reproductive type in the other species of the genus Phymatopteris. Based on our study and previous data, the significance of chromosome number in phylogenetic study was discussed.     

国产12种苔藓植物的染色体数目

报道了中国产12种苔藓植物染色体数目,结果为:壶苞苔Blasia pusilla,n=9;艳绿光苔Cyathodium smaragdinum,n=9;紫背苔Plagiochasma rupestre,n=9;石地钱Reboulia hemisphaerica,n=9;宽片叶苔Riccardia latifrons,n=10;尖叶美喙藓Eurhynchium eustegium,n=11;东亚沼羽藓Helodium sachalinense,n=11;白齿藓Leucodon sciuroides,n=11     

A new Dryopteris (Pteropsida: Dryopteridaceae) species from south-central Africa

Dryopteris katangaensis , a new species endemic to the Katango–Zambian centre of endemism (Congo-Zambezi watershed) in Zambia and the Democratic Republic of Congo is described and illustrated. The morphological differences between the new species and D. schimperiana are discussed, and the ferns endemic to the Katango–Zambian Centre are reviewed.  © 2003 The Linnean Society of London, Botanical Journal of the Linnean Society , 2003, 142 , 237–242.     

New species in the fern genus Dryopteris (Dryopteridaceae) from the islands in the Gulf of Guinea (West Africa)

Three new species of Dryopteris, D. cicatricata J.P. Roux and D. caperata J.P. Roux from São Tomé and D. aurantiaca J.P. Roux from Annobón are described. All three taxa appear to be local endemics. A key to the Dryopteris species occurring on the islands in the Gulf of Guinea is provided.     

Chromosome numbers in the genus Lippia (Verbenaceae)

The genus Lippia (Verbenaceae) comprises about 200 taxa mainly distributed in Brazil, Mexico, Central America, Africa, Argentina and Paraguay. Some problems involving the number and delimitation of species have been reported. In order to contribute to the solving of these problems, the chromosome numbers of 14 Lippia species are documented. The following species were collected at Espinhaço Range, Southeast Brazil: Section Zapania (L. corymbosa, L. diamantinensis, L. hermannioides, L. lacunosa, L. rotundifolia, L. rubella), section Rhodolippia (L. florida, L. lupulina, L. pseudothea, L. rosella), section Goniostlachyum (L. glandulosa, L. pohliana, L. sidoides) and section Dioicolippia (L.filifolia). Immature inflorescences were collected and the ideal size for chromosome observation was determined. The majority of species have a haploid chromosome number from 10 to 14. Few species have a higher chromosome number, which suggests the occurrence of polyploidy. The relationships between chromosome numbers and the taxonomic sections are also discussed.     

A revision of Dryopteris sect. Diclisodon (Dryopteridaceae) based on morphological and molecular evidence with description of a new species

Dryopteris sect. Diclisodon is a small section of ferns with about 12 species mainly distributed in East Asia. Here, we carried out morphological and phylogenetic analyses of this section. A new species from southwest China, D. gaoligongensis, is described and illustrated. Dryopteris gaoligongensis resembles D. indonesiana and D. sparsa, but differs by having a creeping rhizome and large 4-pinnate fronds. We also show that D. glabrior Ching & Z.Y. Liu is a distinct species; however, because it is a later homonym of D. glabrior Copel., it should be renamed D. renchangiana. We conclude that a species previously known as D. nitidula, also an illegitimate homonym, should be recognized with a new name, D. sinonepalensis. We resolve the phylogenetic position of D. yoroii as sister to other sampled species of D. sect. Diclisodon. Our phylogenetic analyses confirm the distinctiveness of D. gaoligongensis, D. renchangiana, and D. sinonepalensis. A key to species of D. sect. Diclisodon in China is provided.     

Karyological studies on the Sino-Himalayan genus, Cremanthodiurn (Asteraceae: Senecioneae)

Twenty-two populations of seven species of Cremanthodium from high altitude regions of western China were observed karyologically. C. ellisii, C. microglossum, C. brunneo-pilosum, C. stenoglossum, C. discoideum and C. lineare all had the same chromosome number of 2 n = 58 whereas C. humile had 2 n = 60. All chromosome numbers of these species are documented here for the first time. The basic number of x = 30 is new for this genus. The karyotypes of all species belong to 2A type according to Stebbins' asymmetry classification of karyotypes. Two basic chromosome numbers, x = 30 and x = 29 in Cremanthodium , correspond exactly to two branching patterns in this genus, sympodial versus monopodial. The systematic and taxonomic statuses of the sympodial species need further study. The karyomorphological data provide no support to the sectional subdivision in Cremanthodium .