中国蹄盖蕨属的研究I─属下分类

蹄盖蕨属是蕨类植物中分类最困难的大属之一,中国、喜马拉雅和日本为其分布中心。隶属于本属的种实际上是由蹄盖蕨科或广义蹄盖蕨属中其他属被划分出去以后剩余下来的种类集合而成的“大杂烩”,因此,它们被放在一起并非是一个单系起源的自然类群;属下不同类群分化的程度相差也很大,有的类群进化活跃,近缘种很多,有的类群则很孤立,所以属下单位所包括的种数相差悬殊;孢子周壁表面褶皱的有无在本属的属下分类中占有重要的位置。已发表的中国蹄盖蕨属植物名称约有３００多个,它们初步被处理为１１７种和一些变种和杂种,本文建议把这些种分为１４个组和１５个系。     

中国蹄盖蕨属轴果蹄盖蕨系的研究

本文是中国蹄盖蕨属植物研究的系列论文的第三篇,对国产轴果蹄盖蕨系植物进行了分类学订正,详细记载了中国产该系植物11种,首次将20余个名称归入该系的一些种下做为异名处理。轴果蹄盖蕨系植物是蹄盖蕨属中自然的一群,以其铁角蕨类型的孢子囊群和囊群益与其它属下类群相区别。本系植物分布于亚洲热带和亚热带山地,常见于山地常绿阔叶林下,海拔500～1800m。在华中和华东地区其分布区北界不超过长江一线。中国西南地区和台湾及日本为该系的三个分化中心。     

蹄盖蕨属（Athyrium Roth）分类性状观察

通过查阅馆藏标本和野外观察,对蹄盖蕨属（Athyrium Roth）的分类性状进行了比较研究,认为根状茎类型、叶上是否具刺、孢子囊群的形状、羽片基部上侧是否具耳状突起和是否具棘头状腺毛等5个形态性状较为稳定,可作为蹄盖蕨属的属下分类性状;叶或羽片的形状及羽片是否具柄等性状可作为分种性状;叶的分裂回数、鳞片和叶柄、羽轴及小羽轴的颜色、被毛多寡及裂片形状等形态性状不适合单独作为蹄盖蕨属属内分种的性状。     

山东产蹄盖蕨科2属植物形态解剖学的研究

采用光镜和扫描电镜对山东分布的蹄盖蕨科2属(蹄盖蕨属和假蹄盖蕨属)7种植物的根、根茎、叶柄、叶轴、叶表皮、表皮毛和孢子囊进行了形态解剖学的系统研究.结果表明,在形态解剖学方面2属植物的共同特征为:根均为无髓中柱;叶柄基部的双柱型维管束向上渐靠近联合形成1个周韧型维管束;叶上下表皮垂周壁均呈波状;气孔主要为胞环型、周胞型或极附型.2属植物的不同特征是:蹄盖蕨属植物体无毛;而假蹄盖蕨属植物叶片和叶轴上均生有腺毛;蹄盖蕨属植物根皮层外侧为薄壁细胞,假蹄盖蕨属则为棕色厚壁细胞环.研究结果表明蹄盖蕨科为一个自然分类群,并支持假蹄盖蕨属的成立.     

蹄盖蕨科的系统发育: 叶绿体DNA trnL-F区序列证据

蹄盖蕨科Athyriaceae是蕨类植物中一个复杂的大科,由于属间关系不甚清楚,该科分类系统还有一些问题,比如新蹄盖蕨、拟鳞毛蕨属、假冷蕨属、肠蕨属、短肠蕨属和菜蕨属的系统位置常有争议。根据蹄盖蕨科34种植物和3种外类群植物的叶绿体DNA trnL-F区序列建立了系统发育树,结果显示:1.trnL_F区序列分析的结果与rbcL基因序列分析的结果几乎一致。2.新蹄盖蕨属Neoathyrium Ching&Z.R.Wang不应成立,该属应与角蕨属Cornopteris Nakai合并。3.假冷蕨属Pseudo     

黑龙江省蹄盖蕨科(Athyriaceae)植物的RAPD分析及其系统学意义

在形态分类研究的基础上,利用RAPD技术,对黑龙江省蹄盖蕨科植物6属9种共15个种群进行了遗传多样性分析,分析结果表明：（1）假冷蕨属应包括在蹄盖蕨属中（2）角蕨属与蹄盖蕨属,羽节蕨属与冷蕨属亲源关系较近（3）短肠蕨属为独立一属,与其它属亲源关系较远。根据黑龙江省蹄盖蕨科植物的DNA水平的研究结果,再结合其形态学特征,建议将黑龙江省蹄盖蕨科划分为3个亚科：冷蕨亚科(Cystopterioideae)包括2个属：冷蕨属(Cystopteris)和羽节蕨属(Gymnocarpium)。蹄盖蕨亚科(Athyrioideae)包括3个属：蹄盖蕨属(Athyrium)、假冷蕨属(Pseudocystopteris)和角蕨属(Cornopteris)。双盖蕨亚科(Diplazioideae)包括短肠蕨属(Allantodia)。     

中国蹄盖蕨属的研究Ⅱ—种的处理（1）

已发表的涉及中国的蹄盖蕨属植物的名称有300多个,它们初步被处理为117种和一些变种和杂种,全文将分4次报道,本篇是第一部分:分种检索表。     

4种蹄盖蕨科植物配子体形态和发育的比较研究

利用光学显微镜详细观察蹄盖蕨科(Athyriaceae)2属4种植物,即蹄盖蕨属的尖头蹄盖蕨(Athyrium vidalii)、长柄蹄盖蕨(A.longius)和喜马拉雅蹄盖蕨(A.fimbriatum)以及亮毛蕨属的亮毛蕨(Acystopteris japonica)配子体发育过程,记录配子体各发育阶段的特征。4种植物的孢子都为单裂缝,两侧对称,孢子萌发类型为向心型,配子体发育类型为铁线蕨型,性器官都为薄囊蕨型,成熟原叶体为对称的心脏形,无毛状体;种间差异包括孢子纹饰、孢子萌发时间、配子体形成时间、丝状体长度、片状体和原叶体的形态以及性器官大小。     

中国蹄盖蕨属的研究Ⅱ——种的处理(I)

已发表的涉及中国的蹄盖蕨属植物的名称有300多个,它们初步被处理为117种和一些变种和杂种,全文将分4次报道,本篇是第一部分：分种检索表。     

黑龙江省蹄盖蕨科（Athyriaceae）植物的RAPD分析及其系统学意义

在形态分类研究的基础上,利用RAPD技术,对黑龙江省蹄盖蕨科植物6属9种共15个种群进行了遗传多样性分析,分析结果表明：（1）假冷蕨属应包括在蹄盖蕨属中（2）角蕨属与蹄盖蕨属,羽节蕨属与冷蕨属亲源关系较近（3）短肠蕨属为独立一属,与其它属亲源关系较远。根据黑龙江省蹄盖蕨科植物的DNA水平的研究结果,再结合其形态学特征,建议将黑龙江省蹄盖蕨科划分为3个亚科：冷蕨亚科（Cystopterioideae）包括2个属：冷蕨属（Cystopteris）和羽节蕨属（Cemnocarpium）。蹄盖蕨亚科（Athyrioideae）包括3个属：蹄盖蕨属（Athyrium）、假冷蕨属（Pseudocystopteris）和角蕨属（Cornopteris）。双盖蕨亚科（Diplazioideae）包括短肠蕨属（Alhntodia）。     

中国台湾和大陆蹄盖蕨属植物的生物地理学比较

蹄盖蕨属Athyrium Roth是个典型的东亚属,全世界估计约有160种,主要分布在亚洲东部的亚热带高山,少数在温带其他地区,中国有117种,是其分布中心。台湾和大陆的蹄盖蕨属植物关系尤为密切,是研究海峡两岸植物地理关系的一个很好的材料。台湾已知共计有蹄盖蕨类植物32种,包括狭义蹄盖蕨27种,介蕨2种,蛾眉蕨1种,假蹄盖蕨1种,假冷蕨1种,即使将待查实的4种蹄盖蕨除去,至少还有28种。其中除去7种大陆不产外, 21种均和大陆共有,占75%。况且,这7种与大陆种形态相近,是否同种异名、亚种或姊妹种关系还有待进一步研究;在台湾和大陆共有的16种狭义蹄盖蕨中有7种是台湾-西南间断分布。这不仅说明了台湾的蹄盖蕨属类植物和大陆的关系密切、有着共同的起源,而且说明台湾高地的植物区系和西南高地关系最为密切。运用生物系统学和分子系统学的方法研究和测定海峡两岸共有种种内、姊妹种或近缘种之间的遗传学关系(如:遗传一致度),进一步了解并量化台湾和大陆植物区系之间的历史和地理关系是必要的。     

中国蹄盖蕨属植物孢子形态的研究

利用扫描电子显微镜对我国产蹄盖蕨属44种植物的孢子进行了观察。结果表明,该属孢子形态为单裂缝,两侧对称,极面观为椭圆形,赤道面观为豆形。外壁表面光滑,由周壁形成表面纹装饰。根据周壁的结构和表面纹饰,可分为两种类型;一是周壁外层发达,形成粗大的脊状纹饰,有11种属此类型;二是周壁外层很薄或不完全发育,由周壁内层或中层形成表面纹饰,有33种属此类型纹饰。本文还就本属的孢子形态特征以及与本属的属下分类关系、本属与邻近属的关系等进行了讨论。     

湖北蕨类植物区系基本成分和主要特点的探讨

在湖北蕨类植物区系中,属种数量最多的科有水龙骨科(Polypodiaceae)、鳞毛蕨科(Dryopteridaceae)和蹄盖蕨科(Athyriaceae)。并以鳞毛蕨属(Dryopteris)、耳蕨属(Polystichum)和蹄盖蕨属(Athyrium)为最主要代表。区系的主要特点为:种类丰富,地理成分错综复杂,联系广泛,显示出多种区系成分交叉在一起的过渡特色。     

蹄盖蕨属的分类

德国植物学家Roth 1799年根据瑞典植物学家Linnaeus定名的Polypodium filix-femina L.为模式,建立了蹄盖蕨属Athyrium Roth,得到各国植物学家所承认。但一百多年来,由于本属植物形体变异较大,孢子囊群多种多样,属下分类比较困难,以致造成今日学名上的混乱!     

PHYLOGENETIC ANALYSIS OF THE MARINE AND FRESHWATER THALAS-SIOSIROID DIATOMS

The thalassiosiroid centric diatoms are distinguished by at least one synapomorphy, the strutted process or fultoportula. Variously classified as a family (Thalassiosiraceae) or an order (Thalassiosirales) among centric diatoms, it is generally conceded that the group of several hundred fossil and living species is monophyletic as a whole. There are two ecological groups of thalassiosiroids, marine and freshwater. It has been hypothesized, based on an ecletic, non-rigorous, evolutionary taxonomy perspective that both the marine and freshwater ecological groups are also monophyletic, but this hypothesis has never been tested in a rigorous framework. Likewise, the freshwater thalassiosiroid species have been grouped into several genera and subgenera using an evolutionary taxonomic approach, but these hypotheses have not fully been tested using cladistic analysis. Focusing mainly on freshwater species, but including at least one representative of each marine genus and one representative from each of several proposed subgeneric groupings of the genus Thalassiosira , we scored morphological characters for fossil and living marine and freshwater Thalassiosiraceae to test these hypotheses. Our cladistic results provide strong support for monophyly for the freshwater group, but it seems unlikely that the marine group is monophyletic. The cladistic results are corroborated to greater or lesser degrees by the fossil record. The implications for evolution in the group and for taxon sampling in molecular studies we are conducting will be discussed.     

On the systematic position of Athyrium crenulato-serrulatum Makino from North-eastern Asia

The fern Athyrium crenulato-serrulatum Makino is found in the whole of Northeastern Asia embracing Northeastern China, Korea, Japan, Ussuri and the Far East USSR. It is similar to the European Athyrium distentifolium, formerly known as A. alpestre, in having exindusiate round or ovate sori, but differs in several essential characters, such as the well-spaced fronds are biseriately arranged along a thick and long-creeping rhizome, the base of stipe is thickened and not attenuated towards the point of attachment, the deltoid-ovate lamina with the basal pinnae as long as those next above, which all are distinctly petiolate and the rachis, costis and especially the costules of pinnules clad in fine pale-colored generally septate hairs underneath. All these clearly show that the fern in question is not an Athyrium sen. str. neither Pseudoathyrium Newman to which latter the fern was referred by Nakai. However, we have been long suspicious of its proper systematic position. In his recent monograph on the genus Cornopteris (Acta Phytotax. Geobot. 30: 104. 1979.) Kato has pointed out that C.crenulato-serrulata (Makino) Nakai “has the northernmost destribution in the genus and exhibits a few characteristics similar to Athyrium, the swollen base of stipes with projections and cartilaginous lamina margin. By these characteristics the species is clearly discriminated from other species”. According to Kurita (1964), Mitui (1970) and Karo (1978) the species in question has chromosome numbers n=40, the base number of the subfamily Athyrioides instead of x=41, the base number of the subfamily Diplazioides including Cornopteris Nakai. Since thefern in question fits no other athyrid genera, hence a new genus is proposed.     

A molecular phylogeny of Panicum (Poaceae: Paniceae): tests of monophyly and phylogenetic placement within the Panicoideae

Panicum L. is a cosmopolitan genus with approximately 450 species. Although the genus has been considerably reduced in species number with the segregation of many taxa to independent genera in the last two centuries, Panicum remains a heterogeneous assemblage, as has been demonstrated in recent years. The genus is remarkably uniform in its floral characters but exhibits considerable variation in anatomical, physiological, and cytological features. As a result, several classifications, and criteria of what the genus should really include, have been postulated in modern literature. The purpose of this research, based on molecular data of the chloroplast ndhF gene, is to test the monophyly of Panicum, to evaluate infrageneric classifications, and to propose a robust phylogenetic hypothesis. Based on the present results, previous morphological and molecular phylogenetic studies, and inferred diagnostic morphological characters, we restrict Panicum sensu stricto (s.s.) to the former subgenus Panicum and support recognition of Dichanthelium, Phanopyrum, and Steinchisma as distinct genera. We have transfered other species of Panicum to other genera of the Paniceae. Most of the necessary combinations have been made previously, so few nomenclatural changes have been required. The remaining species of Panicum sensu lato (s.l.) are included within Panicum incertae sedis representing isolated species or species grouped within monophyletic clades. Additionally, we explore the performance of the three codon position characters in producing the supported phylogeny.     

POLLEN MORPHOLOGY AND SYSTEMATICS OF SIPHONOGLOSSA SENSU LATO (ACANTHACEAE)

Pollen morphology of 15 species of Siphonoglossa and of two closely related groups was investigated. Two tribal-specific pollen types are found within Siphonoglossa sensu lato suggesting that the genus is artificial, composed of taxa belonging in several genera among two tribes (subtribes sensu Bremekamp) of Acanthaceae. Five taxa currently included in an informal subgeneric category of Siphonoglossa have tricolporate, prolate pollen (termed Type I) that is characteristic of Odontonemeae (= Odontoneminae, Justicieae). Pollen of the remaining taxa, belonging in two formal sections of the genus, are mostly 2-porate, bilateral (Type II) with a sexine sculpturing characteristic of Justicieae (= Justiciinae). Pollen of section Siphonoglossa is rather uniform, 2-porate, bilateral with lolongate pores, and seem to delimit a natural group. Taxa of section Pentaloba have a more heterogeneous pollen morphology, mostly 2-porate, bilateral with lalongate pores. Controversial aspects of the interpretation of pollen morphology in Justiciinae are presented and their relevance to this study are examined. Hypothetical trends in the evolution of pollen of Justiciinae are discussed and the application of pollen morphology to taxonomy of the genus is presented, including a recommendation for narrowing the generic concept of Siphonoglossa to the taxa of the type section.