珍稀水生植物——宽叶泽苔草的核型研究

宽叶泽苔草（Caldesia granis Samuel）。是一种珍稀濒危水生植物。它曾经一度被认为已经从中国大陆灭绝,但最近又在湖南省的一个高山沼泽中被发现。本文首次报道了依据上述新发现地点的宽叶泽苔草材料进行的细胞学研究结果。核型分析结果表明：本种染色体数目为22,其染色体组型高度不对称。结合前人对宽叶泽苔草一些近缘种的细胞学及古生物学研究结果,作者认为泽苔草属植物很可能是泽泻科中最进化的一个属。     

宽叶泽苔草萜类化学成分分析及其化学分类学意义

宽叶泽苔草Caldesia grandis隶属泽泻科Alismataceae,是一种珍稀濒危水生植物。其化学成分迄今未见报道。本文利用气质联用的方法鉴定了该植物的43种化学成分,并总结了已报道的其近缘泽泻属Alisma、慈姑属Sagittaria、刺果泽泻属Echinodorus植物的化学成分,据此进行化学分类学分析:它们的特征化学成分是二萜,宽叶泽苔草和泽泻属植物的二萜成分是处于二萜生源合成途径最顶端的kaurane类型;慈姑属植物的二萜成分既有处于该途径底端的clerodane型、中间的pimarene型,也有顶端的kaurane型、abietene型二萜;刺果泽泻属植物的二萜成分是处于该途径底端的clerodane型。宽叶泽苔草和泽泻属植物都有桉叶烷型和愈创木烷型的倍半萜。因此宽叶泽苔草和泽泻属植物的亲缘关系比慈姑属、刺果泽泻属植物的近,由此推测它们的进化层次可能依次是刺果泽泻属植物、慈姑属植物、泽泻属植物、宽叶泽苔草。     

泽苔草的花器官发生

本文用扫描电镜观察了泽苔草的花器官发生过程,观察结果表明：花萼以螺旋状方式向心发生,花瓣以接近轮状方式近同时发生,不存在花瓣雄蕊复合原基。雄蕊和心皮均以轮状向心方式发生,6枚雄蕊分两轮分别在对萼和对瓣的位置先后发生,至发育的后期排成一轮,但仍分别处于对萼和对瓣的位置;随后发生的第一轮3个心皮原基与3枚萼片相对,第二、三轮心皮原基分别为1~3个,与前一轮心皮相间排列向心发生。本文首次揭示了泽苔草花被的外轮3个萼片螺旋状发生方式,这种螺旋状方式很可能是泽泻科植物的花部结构在进化过程中适应环境而保留下来的一种较原始的叶性特征。     

太原黄耆(豆科)花器官及胚珠发育研究

太原黄耆是新近发表的物种,分布于中国陕西和山西。该实验利用扫描电子显微镜对太原黄耆的花器官发生和发育过程进行观察研究。结果显示:(1)太原黄耆的各轮花器官都是从远轴端向近轴端单向连续发生,在不同轮之间存在花器官重叠发生的现象。(2)在花的发育过程中,出现2种共同原基,即初级共同原基和次级共同原基,由初级共同原基发育成对萼雄蕊原基和次级共同原基,再由次级共同原基发育成花瓣原基和对瓣雄蕊原基。(3)雄蕊管近轴端基部开口是在进化过程中产生的特殊结构,是一种对传粉者的适应机制,从而有利于传粉活动的进行。(4)胚珠为倒生胚珠,具有2层珠被,认为倒生胚珠是内外2层珠被共同作用的结果。     

花叶芋(天南星科)的花器官发生

利用扫描电镜首次观察了天南星科花叶芋(Colocasia bicolor) 的花器官发生过程。花叶芋的肉穗花序由无花被的单性花构成, 雌花发生于花序基部, 雄花发生于花序上部, 中性花位于花序中间部位。雄花: 3 或4 个初生雄蕊原基轮状发生, 随后每个初生原基一分为二, 形成6或8个次生原基; 一部分次生原基在其后的发育过程中融合, 形成5 或7 枚雄蕊; 雄花发育过程中未见雌性结构的分化; 花药的分化先于花丝; 雄蕊合生成雄蕊柱。雌花: 合生心皮, 3或4个心皮原基轮状发生, 未见雄性结构的分化。中性花来源于雌雄花序过渡带上, 属于雄蕊原基的滞后发育以及发育成熟过程中的退化; 与彩叶芋属(Caladium)不同, 此过渡区未见畸形两性花。初生雄蕊原基二裂产生次生原基的次生现象在目前天南星科花器官发生中显得比较特殊, 同时初步探讨了次生原基的融合方式。     

桂味荔枝花器官的发生和发育过程研究

利用SV11立体显微镜和JSM-6360LV型扫描电镜观察‘桂味’荔枝花器官的发生和发育过程。结果表明:花序原基最先发生,然后形成数个大小不等的单花原基;4个萼片原基的发生不同步,其中一侧对位先发生;6～10枚雄蕊原基以轮状方式几乎同时发生;心皮原基最后发生,2～3枚(稀4枚)心皮原基同时出现,随后进行侧向生长,逐渐合拢形成子房。雌花中,花柱、柱头分化明显,雄蕊退化。雄花中,花丝细长,花药饱满,雌蕊退化或发育不完全。两性花中,雌雄蕊发育完全。花粉粒近球形,具3孔沟,表面为条纹状纹饰。     

毛舞花姜花器官的发生与发育

通过扫描电镜观察了毛舞花姜(Globba barthei Gagne p.)的花序及花器官的发生与发育。3枚萼片原基首先于花顶连续发生,随后花顶的中心凹陷形成环状原基,环状原基进一步分化形成三枚花瓣—雄蕊共同原基,并在花顶的中心形成花杯。共同原基分化形成花瓣和三枚内轮雄蕊,紧接着外轮雄蕊在花杯的顶点发生。远轴的两枚内轮雄蕊延伸生长并相互融合形成了唇瓣,近轴的一枚形成了可育雄蕊;近轴的两枚外轮雄蕊发育形成了成熟花结构中的侧生退化雄蕊,而远轴的一枚缺失。近轴的两枚外轮雄蕊原基起始的同时,3枚心皮原基也在中心花杯的内侧发生而后与外轮雄蕊相间排列。对毛舞花姜花序的发生和发育的观察发现,在花序轴的头几片初级苞片中产生的是珠芽原基而非蝎尾状小花序原基,其形态特征类似于早期的蝎尾状小花序原基,由此推测珠芽很可能是蝎尾状小花序的变异。     

臭椿花器官分化的初步研究

利用扫描电镜(SEM)和光镜(LM)对臭椿花序及花器官的分化和发育进行了初步研究,表明:1)臭椿花器官分化于当年的4月初,为圆锥花序;2)分化顺序为花萼原基、花冠原基、雄蕊原基和雌蕊原基。5个萼片原基的发生不同步,并且呈螺旋状发生;5个花瓣原基几乎同步发生且其生长要比雄蕊原基缓慢;雄蕊10枚,两轮排列,每轮5个原基的分化基本是同步的;雌蕊5,其分化速度较快;3)在两性花植株中,5个心皮顶端粘合形成柱头和花柱,而在雄株中,5个心皮退化,只有雄蕊原基分化出花药和花丝。本研究着重观察了臭椿中雄花及两性花发育的过程中两性花向单性花的转变。结果表明,臭椿两性花及单性花的形成在花器官的各原基上是一致的(尽管时间上有差异),雌雄蕊原基同时出现在每一个花器官分化过程中,但是,可育性结构部分的形成取决于其原基是否分化成所应有的结构:雄蕊原基分化形成花药与花丝,雌蕊原基分化形成花柱、柱头和子房。臭椿单性花的形成是由于两性花中雌蕊原基的退化所造成,其机理有待于进一步研究。     

宽叶泽苔草居群内遗传多样性研究

(武汉大学生命科学学院植物系统学与进化生物学研究室,武汉430072)摘要:采用RAPD分子标记对宽叶泽苔草(Caldesiagrandis)湖南浪畔湖居群30个家系共180个子代样品进行了居群内家系间以及家系内的遗传多样性分析。从100个随机引物中筛选出12个有效引物,共产生112条带,其中79条表现出多态性,占总条带数的70.5%。宽叶泽苔草各个家系多态位点百分率(PPB)在7.1%–40.2%之间。各个家系基因多样性范围在0.02–0.14之间(家系水平的基因多样性为0.10),Shannon指数的范围在0.04–0.21之间(家系水平的Shannon指数为0.18)。对宽叶泽苔草30个家系的AMOVA分析结果显示,家系间的基因分化系数Gst=0.231,即总的变异中有23.1%的变异存在于家系间,家系内的遗传变异占总遗传变异的76.9%,家系间和家系内变异均极显著(P<0.001)。采用UPGMA法对宽叶泽苔草30个家系180个子代进行聚类的结果表明:同一家系的子代个体并不能完全聚在一起。基于家系间的遗传分化系数Gst对宽叶泽苔草30个家系间的基因流进行估测,结果显示:Nm=0.83,表明宽叶泽苔草各个家系之间有较高的基因流。     

Floral organogenesis of Caldesia grandis Samuel. (Alismataceae)

The floral organogenesis of Caldesia grandis Samuel. was observed under scanning electron microscope (SEM). The primordia of the floral appendage were arranged according to a trimerous plan and in acropetal succession. Three sepal primordia were first ini     

Developmental study on the inflorescence and flower of Caldesia grandis Samuel (Alismataceae)

The inflorescence and floral development of Caldesia grandis Samuel is reported for the first time in this paper. The basic units of the large cymo‐thyrsus inflorescence are short panicles that are arranged in a pseudowhorl. Each panicle gives rise spirally to three bract primordia also arranged in a pseudowhorl. The branch primordia arise at the axils of the bracts. Each panicle produces spirally three bract primordia with triradiate symmetry (or in a pseudowhorl) and three floral primordia in the axils of the bract primordia. The apex of the panicle becomes a terminal floral primordium after the initiations of lateral bract primordia and floral primordia. Three sepal primordia are initiated approximately in a single whorl from the floral primordium. Three petal primordia are initiated alternate to the sepal primordia, but their subsequent development is much delayed. The first six stamen primordia are initiated as three pairs in a single whorl and each pair appears to be antipetalous as in other genera of the Alismataceae. The stamen primordia of the second whorl are initiated trimerously and opposite to the petals. Usually, 9–12 stamens are initiated in a flower. There is successive transition between the initiation of stamen and carpel primordia. The six first‐initiated carpel primordia rise simultaneously in a whorl and alternate with the trimerous stamens, but the succeeding ones are initiated in irregular spirals, and there are 15–21 carpels developed in a flower. Petals begin to enlarge and expand when anthers of stamens have differentiated microsporangia. Such features do not occur in C. parnassifolia. In the latter, six stamen primordia are initiated in two whorls of three, carpel primordia are initiated in 1–3 whorls, and there is no delay in the development of petals. C. grandis is thus considered more primitive and C. parnassifolia more derived. C. grandis shares more similarities in features of floral development with Alsma, Echinodorus, Luronium and Sagittaria. © 2002 The Linnean Society of London, Botanical Journal of the Linnean Society, 2002, 140 , 39–47.     

The flora of the early Miocene Brandon Lignite, Vermont, USA. VIII. Caldesia (Alismataceae)

Caldesia, a genus of aquatic monocotyledons, is represented by four living species, which are widely distributed in the temperate and tropical Old World. The genus has an extensive Oligocene through Pleistocene fossil record in Eurasia. We survey the morphology of the extant and fossil fruits of the Alismataceae, and provide a detailed review of the morphology and anatomy of living and fossil Caldesia fruits. The latter exhibit substantial similarity, making the recognition of separate species on the basis of fruit morphology difficult. We erect the new species Caldesia brandoniana from the Early Miocene Brandon Lignite of Vermont primarily on the basis of its geographic isolation; careful revision of all fossil fruiting material of Caldesia might require placement of the Brandon specimens in a more inclusive form species. Together with leaves of Caldesia from the Miocene Clarkia flora of Idaho, this occurrence indicates that Caldesia was in the New World as recently as the Early Miocene.     

Chemical analysis of diterpenoids in Caldesia grandis and its chemotaxonomic implication

Caldesia grandis is a rare and endangered aquatic plant of the Alismataceae family. This paper first reports 43 chemical components of C. grandis based on the gas chromatography-mass spectrometry and reviews research on the chemical compositions of some closely related genera such as Alisma, Sagittaria, and Echinodorus. Their common chemical components are diterpenoids. Kaurane diterpenoids are found in Caldesia, Alisma and Sagittaria; clerodane diterpenoids in Sagittaria and Echinodorus; and pimarene and abietene diterpenoids in Sagittaria. By the biogenesis of diterpenoids, kaurane and abietene diterpenoids represent evolutionarily derived compounds, clerodane diterpenoids are primordial, and pimarene diterpenoids are intermediate. The chemotaxonomy, karyotypical analysis and fossil records of those genera showed that Caldesia was evolutionarily closer to Alisma than to Sagittaria and Echinodorus. Possible evolution levels of Echinodorus, Sagittaria, Alisma, Caldesia in chronological order are derived.     

灌木铁线莲（毛茛科）花器官的发生与发育

用扫描电子显微镜（SEM）对铁线莲属（Clematis L.）植物灌木铁线莲(C. fruticosa Turcz.)花的形态发生和发育过程进行了观察。灌木铁线莲花原基形成后,4枚萼片以交互对生的方式首先发生,呈轮状排列。最早的4枚雄蕊原基在4枚萼片交接的位置上近螺旋状发生,此后,随着雄蕊原基的向心发生和数目不断增多,其发生的螺旋状序列逐渐明显。雄蕊原基发生后,在花原基顶端,心皮原基沿着雄蕊原基的发生序列呈螺旋状发生。本文结果支持在原始被子植物花中螺旋状排列和轮状排列同时存在的观点。此外,本文也进一步证实了花萼与苞片的同源性。     

商陆属植物的花器官发生

为进一步研究商陆科的系统位置提供花器官发生和发育的证据,在扫描电子显微镜下观察了商陆Phytolacca acinosa、多雄蕊商陆P. polyandra和垂序商陆P. americana的花器官发生.结果表明: 商陆属植物花被的发生均为2/5型螺旋发生.在同一个种不同的花蕾中,花被的发生有两种顺序:逆时针方向和顺时针方向.远轴侧非正中位的1枚先发生.雄蕊发生于环状分生组织.在单轮雄蕊的种中8-10枚雄蕊为近同时发生;两轮雄蕊的种8枚内轮雄蕊先发生,6-8枚外轮雄蕊随后发生,内轮雄蕊为同时发生,外轮雄蕊发生次序不规则.心皮原基也发生于环状分生组织,8-10枚心皮原基为同时发生.在后来的发育过程中,商陆的心皮发育成近离生心皮雌蕊;其他2种心皮侧壁联合发育成合生心皮雌蕊.对商陆属植物花器官发生的类型及发育形态学做了分析,结果支持商陆科在石竹目系统发育中处于原始地位的观点.