3种龙葵表皮毛类型及发育过程观察研究

通过观察发现龙葵（Ｓｏｌａｎｕｍ ｎｉｇｒｕｍ Ｌ．）、少花龙葵（Ｓ．ｐｈｏｔｅｉｎｏｃａｒｐｕｍ Ｎａｋａｍ,ｅｔＯ－ｄｓｈｉ）和黄果龙葵（Ｓ．ｎｉｇｕｍ Ｌ．ｖａｒ．ｓｕａｖｅｏｌｅｎｓ Ｇ．Ｌ．Ｇｕｏ）的表皮毛均为腺毛,主要有单细胞头腺毛和多细胞头腺毛２种。腺毛的原始细胞都来源于原表皮细胞,经２次平周分裂产生基细胞、柄细胞和顶端细胞、在腺毛后期的形态发生中,柄细胞和顶细胞的分裂状态决定腺毛的     

紫苏腺毛的形态发生研究

紫苏叶上有两种腺毛：质状腺毛和头状腺毛。两者都具１个基细胞、１个柄细胞和头部。前者的头部可由１、２、４或８个分泌细胞组成,扩展成质状;后者的头部由１、２或４个分泌细胞组成,聚成圆球状。两种腺毛的原始细胞都来源于原表皮细胞,经两次平周分裂产生基细胞、柄细胞和顶细胞。在腺毛后期的形态发生中,柄细胞的分化状态决定腺毛的类型。若柄细胞保持扁平关且处于分生状态时,其顶细胞将发育成质状腺毛的头部;若柄细胞纵向     

紫苏腺毛的形态发生研究

紫苏叶上有两种腺毛:盾状腺毛和头状腺毛。两者都具1个基细胞、1个柄细胞和头部。前者的头部可由1、2、4或8个分泌细胞组成,扩展成盾状;后者的头部由1、2或4个分泌细胞组成,聚成圆球状。两种腺毛的原始细胞都来源于原表皮细胞,经两次平周分裂产生基细胞、柄细胞和顶细胞。在腺毛后期的形态发生中,柄细胞的分化状态决定腺毛的类型。若柄细胞保持扁平状且处于分生状态时,其顶细胞将发育成盾状腺毛的头部;若柄细胞纵向引长并迅速液泡化时,其顶细胞将发育成头状腺毛的头部。     

9种榆科植物叶表皮结构特征研究

利用叶表皮离析法观察了榆科6属9种植物叶片的表皮结构。结果表明,榆科植物叶片气孔器仅分布在远轴面,不规则型,不具副卫细胞;叶片毛状体主要有腺毛和非腺毛两种类型,腺毛由基细胞、柄细胞和膨大的顶细胞构成,非腺毛均由单细胞发育而来,基部具或不具钟乳体,多数非腺毛顶部发育成长锥状,少数非腺毛顶部极短呈喙状。根据气孔器的类型和分布位置,尤其是表皮毛的基本结构和发育类型等特征,不支持将广义榆科分为两个独立科的观点。但榆科这9种植物叶表皮特征具有属间或种间差异,有一定的分类学价值。     

羽叶薰衣草表皮毛的发育解剖学研究

对羽叶薰衣草(LavandulapinnataL.)茎和叶上两种表皮毛(腺毛和非腺毛)发育的解剖学观察表明,两者的发生都源于茎或叶的原表皮细胞,但外部形态、发育过程及功能明显不同。腺毛有头状腺毛和盾状腺毛两种类型,均由1个基细胞、1个柄细胞和头部细胞构成。头状腺毛的头部只有1个或2个分泌细胞,盾状腺毛由8个分泌细胞构成头部。非腺毛由3-20个细胞组成,可分为三种类型:单列不分枝、二叉分枝和三叉及三叉以上多分枝的树状分枝。非腺毛的顶部细胞由基部到顶部逐渐变细,先端成尖形。腺毛发育由原表皮细胞经两次平周分裂形成,由于柄细胞和头部细胞所处的分化状态不同而发育成两类腺毛。非腺毛由非腺毛原始细胞经二次或多次平周分裂和不均等分裂,再发育成数个至二十多个子细胞。     

华南地区六种蕨类植物耐旱性研究

利用盆栽控水法研究了华南毛蕨、蜈蚣蕨、线羽凤尾蕨、毛叶铁线蕨、长叶肾蕨和普通针毛蕨6种华南地区常见蕨类的耐旱性,测定了植株在自然干旱下的土壤绝对含水量、叶绿素SPAD值、叶片相对含水量和气体交换参数等指标变化。结果表明:随干旱胁迫加剧,叶片相对含水量总体呈下降趋势,其中普通针毛蕨、蜈蚣蕨和长叶肾蕨下降不明显,华南毛蕨降幅最大。叶绿素SPAD值随干旱加剧显著下降,其中华南毛蕨和长叶肾蕨下降幅度较小,蜈蚣蕨下降幅度较大。净光合速率、气孔导度和蒸腾速率随干旱加剧而不断下降,其中普通针毛蕨和蜈蚣蕨下降幅度较小,华南毛蕨下降幅度较大。然而,胞间CO2浓度随着干旱的加剧而不断上升,其中线羽凤尾蕨上升幅度最大,蜈蚣蕨和普通针毛蕨上升幅度较小。以各指标的平均变化速率为原始数据进行隶属函数法分析得出,六种参试蕨类植物的耐旱能力大小依次为蜈蚣蕨普通针毛蕨长叶肾蕨毛叶铁线蕨华南毛蕨线羽凤尾蕨。     

Development of the glandular and non-glandular leaf hairs of Avicennia marina (Forsskål) Vierh.

The course of development of the glandular and non-glandular hairs of Avicennia marina was found to be the same up to the three-celled stage. The further cell divisions of the two types of developing hairs differed in their orientation. In the non-glandular hair the cells continued to divide transversely, whereas in the glandular hair the uppermost of the three cells divided longitudinally.
In the mature hairs of both types, the peripheral wall of the cell just above the basal cell was heavily cutinized. The existence of narrow canals in the cuticle of the secretory cells of the glandular hairs was confirmed. The homology of the glandular and non-glandular hairs is discussed and it is concluded that the two types are phylogenetically related.     

Glandular Hair Formation in Origanum Species

Eleven Origanum species were investigated in this study. Inall these species, leaf glandular hairs have the same structureand they have been found to follow a common developmental pattern.They originate from a single protodermal cell which dividessuccessively parallel to leaf surface to give rise to the footcell, the stalk cell and the mother cell of the head. The latterundergoes a series of symmetric and asymmetric anticlinal divisionsresulting in a 12-celled head (four small cells in the centreand eight large cells peripherally arranged). Determinationof the glandular scale morphology within the Lamiaceae generaand further comparison between the various gland types wouldbe helpful to systematics. Origanum species, Lamiaceae, glandular hair, development     

Extracellular Matrix Components Regulating Glandular Differentiation and the Formation of Basal Lamina of a Human Pancreatic Cancer Cell Line in Vitro

The interaction between the extracellular matrix and human tumor-cell clones S2-013 and S2-020, derived from a pancreatic cancer cell line (SUIT-2), was examined in vitro, using various cell differentiation-promoting matrices in two- and three-dimensional cultures. S2-013 cells (well-differentiated tubular adenocarcinoma in xenografts in nude mice) cultured in Matrigel formed glandular structures. Ultrastructural observation revealed a morphological polarity of cells and a distinct basal lamina. On the other hand, S2-020 cells (poorly differentiated tubular adenocarcinoma in xenografts) cultured in Matrigel formed neither glandular structures nor a basal lamina, but only cell aggregates. The morphology of these two sublines cultured in Matrigel expressed the histological degree of differentiation which they presented in nude mice. In contrast, in type I collagen gel, S2-013 cells formed glandular structures without a basal lamina, and in soft agar, they were able to form neither glandular structures nor a basal lamina. S2-020 cells cultured in type I collagen gel or soft agar formed the same simple cell aggregates as in Matrigel. Matrices used in a three-dimensional culture influenced the degree of differentiation in S2-013 cells but had no effect on the morphological differentiation in S2-020 cells. To detect the factors which induce basal lamina formation, S2-013 cells were cultured on a microporous membrane coated with extracellular matrix components such as laminin, type IV collagen, and fibronectin. S2-013 cells formed a basal lamina only on the laminin. These cell lines may be useful in investigating the mechanisms regulating the formation of glandular structures and basal lamina.     

C4荒漠植物猪毛菜与木本猪毛菜的叶片解剖结构及光合生理特征

 为了比较C₄荒漠植物猪毛菜(Salsola collina)和木本猪毛菜(S. arbuscula)的抗旱结构和适应环境的光合作用特征, 在二者混生的群落中, 选择代表性植株, 采集叶片进行叶片解剖结构分析, 在自然条件下测定了二者叶片的气体交换参数。研究结果表明：猪毛菜叶片具表皮毛, 具有更发达的薄壁贮水组织;木本猪毛菜叶片具有更厚的角质层, 表皮下有1层下皮细胞, 其栅栏组织细胞较长, 排列更紧密。猪毛菜的净光合速率明显高于木本猪毛菜, 日平均值分别为21.5和15.7 μmol CO₂·m^–2·s^–1。猪毛菜的蒸腾速率也明显高于木本猪毛菜, 日平均值分别为14.9和10.2 mmol·m^–2·s^–1。猪毛菜和木本猪毛菜的水分利用效率的日平均值分别为1.39和1.53 μmol CO₂·mmol^–1 H₂O, 特别是在14:00时分别为1.61和2.30 μmol CO₂·mmol^–1 H₂O, 木本猪毛菜高出猪毛菜约42%。猪毛菜的光补偿点低于木本猪毛菜, 而光饱和点和光量子效率较高, 具有更低的CO₂补偿点。这表明：二者的旱生结构不同, 木本猪毛菜具有更显著的荒漠植物特征;在适于二者混生的环境下, 猪毛菜比木本猪毛菜的光合能力更强, 而木本猪毛菜的水分利用效率更高。     

Leaf micromorphology and leaf glandular hair ontogeny of Myoporum bontioides A. Gray

Myoporum bontioides A. Gray (Myoporaceae), a red list plant in Japan, is restricted to only a few East Asian countries like China, Japan and Taiwan, associated to some true mangroves. The leaf is isolateral and has a thick cuticle; stomata are anomocytic, sunken and have a beak‐shaped cuticular outgrowth at the inner and outer side of the stomatal pore (ledges); profuse glandular hairs are scattered on both leaf surfaces of young leaves. The mesophyll is compact with palisade and spongy parenchyma cells in the young stage, but at maturity profuse intercellular spaces can be observed. Secretory ducts occur in young leaves. Pear‐shaped glandular hairs protrude from the epidermal layer. Hair primordia are well distinct by their larger size and undergo divisions to produce two laterally placed basal cells, two stalk cells and four radiating terminal cells. The cuticle layers of the terminal cells are often separated from the cell wall to form a space, in which ions accumulate for excretion. Inner walls of the basal cells are connected with the mesophyll. Though ontogeny and structure of glandular hairs have resemblance to typical mangroves, considering leaf micromorphology, this plant is better termed as “mangrove associate” instead of “true mangrove”. (© 2013 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

我国荒漠不同生态类型植物的旱生结构

本文研究了我国荒漠15种不同类型植物的解剖结构。结果表明,超旱生和旱生植物具有典型的旱生结构,尤以超旱生植物明显,例如沙冬青、梭梭。 旱生结构的基本特征是：叶片及角质层厚,具表皮毛、腺毛、瘤状或乳状突起,气孔下陷,栅栏组织及贮水组织发达,构成等面叶及肉质叶,具含晶细胞和粘液细胞;维管束鞘、维管束帽及纤维细胞的存在,增强了植株的坚固性。中生植物叶片及角质层较薄：气孔平置或拱起,栅栏组织及海绵组织同等发育,胞间隙大,为背腹叶,这是典型的中生结构。     

紫苏腺毛的形态结构和发育的研究

紫苏（Perillafrutescens（L．）Britton）叶上腺毛的研究表明：叶上腺毛主要有两种类型,一是头状腺毛,二是后状腺毛。两类腺毛都是由1个基细胞、1个柄细胞和由分泌细胞组成的头部构成。头状腺毛的头部由1个、2个或4个分泌细胞构成,其头部呈圆球形或半圆球形。盾状腺毛的头部也由1个、2个、4个或8个分泌细胞构成,其分泌细胞横向扩展使头部呈盾状。分泌盛期,大量分泌物充满角质层下间隙。两类腺毛的原始细胞均起源于叶原基或幼叶的原表皮层细胞,它通过两次平周分裂形成1个基细胞、1个柄细胞和1个头细胞,头细胞不分裂或依次进行1—3次垂周分裂,分别形成单细胞、2细胞、4细胞或8细胞的头部。     

Gametophytes of some Ceylonese species of Thelypteridaceae

Gametophytes of 12 species of the family Thelypteridaceae were investigated with Cryo-SEM and conventional SEM. Most of the species have rounded front lobes and rounded lobes extending backwards. Metathelypteris flaccida has a cordate game-tophyte. All species have glandular hairs, which are of different length and could be used as diagnostic character in some cases. In addition 7 of the species investigated have acicular hairs. In Thelypteris confluens the glandular hairs on margins and surfaces are born on cells that protrude from the surrounding cells. It is concluded that the combination of characters makes it possible to distinguish species of different genera with the help of gametophyte characters only.     

Structures, Components and Functions of Secretory Tissues in Houttuynia cordata

Houttuynia cordata Thunb., traditionally used as a therapeutic plant in folk medicine, has shown antioxidant and anticancer activities. The species, as a core component of paleoherbs, is normally characterized based on the presence of different types of secretory tissue： oil cells, three types of secretory cells and glandular hairs. The aim of this work was to study the structural, componential, and the functional characteristics of the secretory tissues in both the floral and vegetative parts. The results indicate that oil cells and secretory cells are distributed in all organs of the plant, while glandular hairs are situated on the aerial stems and leaves. Both oil cells and glandular hairs initiate from the protoderm, but their developmental processes are different. Although three types of secretory cells initiate from different primary meristems, the developmental patterns of different secretory cells are the same. Also, although the origins of secretory cells are different from oil cells, their early developmental processes are the same. Histochemical results show that oil cells, secretory cells and glandular hairs produce flavonoids, phenolic compounds, tannins, lipids, aldehyde and ketone-compounds. In addition, there are terpenoids and pectic-like substances in oil cells, alkaloids in secretory cells of aerial stems, and terpenoids and alkaloids in glandular hairs. These compounds play very important roles in protecting plants from being eaten by herbivores （herbivory） and infected by microbial pathogens. The oil cell and secretory cell, as unicellular secretory tissues, are intermediates between the primitive surface glandular and secretory cavity and canal during the evolution of secretory structures.     

中国伞形科前胡属果实表面微形态特征及分类学意义

采用扫描电镜方法对中国伞形科(Apiaceae)前胡属(Peucedanum L.) 22种2变种的果实表面微形态特征进行了观察和描述.结果显示:供试种类在果实棱槽细胞平滑度和细胞轮廓可见度、蜡质纹饰类型、细胞表面突起的有无及类型、表皮毛的有无及类型及其纹饰类型、表皮分泌物的有无及类型等方面有明显差异,具有丰富的种间多样性.根据这些特征可将供试种类分为4种类型.类型Ⅰ:棱槽细胞粗糙多毛—细胞轮廓不可见—簇状蜡质纹饰发达,包含滨海前胡(P.japonicum Thunb.)、天竺山前胡(P.ampliatum K.T.Fu)、华北前胡(P.harrysmithii Fedde ex Wolff)及其2变种、长前胡(P.turgeniifolium Wolff)、华山前胡(P.ledebourielloides K.T.Fu)和泰山前胡[P.wawrae (Wolff) Su ex Sheh];类型Ⅱ:棱槽细胞平滑无毛—细胞轮廓不可见或凹陷—条形蜡质纹饰发达或明显,包含芷叶前胡(P.angelicoides Wolff ex Kretschm.)、竹节前胡(P.dielsianum Fedde ex Wolff)、南川前胡[P.dissolutum (Diels)Wolff]、红前胡(P.rubricaule Shan et Sheh)、细裂前胡(P.macilentum Franch.)、前胡(P.praeruptorum Dunn)、华中前胡(P.medicum Dunn)、台湾前胡(P.formosanunt Hayata)、南岭前胡(P.longshengense Shum et Sheh)、会泽前胡(P.acaule Shah et Sheh)和马山前胡(P.mashanense Shan et Sheh);类型Ⅲ:棱槽细胞有稀疏毛—细胞轮廓[陷可见或不明显—蜡质纹饰几无,包含北京前胡(P.caespitosum Wolff)、草原前胡(P.stepposum Huang)、毛前胡(P.pubescens Hand.-Mazz.)和刺尖前胡(P.elegans Komarov);类型Ⅳ:棱槽细胞不平无毛—细胞轮廓呈近圆形凸起—蜡质纹饰为微波状长条形,仅包含石防风[P.terebinthaceum (Fisch.ex Trevir.)Fisch.ex Turcz.]1种.结合外部形态特征以及地理分布对各类型种类的分类关系进行了讨论,并对会泽前胡、马山前胡和石防风的特殊分类地位进行了分析,明确了果实表面微形态特征在前胡属中的分类学意义.     

乌鲁木齐乌头, 新疆毛茛科一新种

该文描述了发现自中国新疆天山北部的毛茛科乌头属一新种,即乌鲁木齐乌头(Aconitm urumqiense),此新种与新疆乌头(A. sinchiangense)近缘。两者的区别在于此新种(乌鲁木齐乌头)的茎无毛,不存在基生叶,总状花序轴和花梗被黄色腺毛,萼片背面疏被柔毛、边缘被缘毛,上萼片较宽,花瓣唇在顶端啮蚀状,子房幼时疏被柔毛。     

Leaf micromorphology and taxonomy of North African species of Sideritis L. (Lamiaceae)

REJDALI M., 1991. Leaf micromorphology and taxonomy of North African species of Sideritis L. (Lamiaceae). This study reports on the structure of trichomes, epidermal cells, stomata and venation patterns. The trichomes are either glandular or eglandular. The latter are unicellular or multicellular, soft or rigid pointed hairs. The glandular hairs are short or long stalked, the latter are generally flattened and may be sessile. The epidermal cells are variously shaped with sinuous or straight walls usually randomly orientated. Stomata are either anomocytic or diacytic and evenly distributed throughout the epidermis without any definite pattern of orientation. Venation is of the semicraspedodermous type.     

Morphology of the Salt Gland of Spartina anglica Hubbard

Apart from roots, rhizome, stem, the adaxial surfaces of the leaf sheaths and palea in the body of the plant of Spartina anglica, the salt glands are found in all other aerial parts, especially, they are abundant in lamina. The gland is composed of two differential cells, a big basal cell and a small, dome- shaped cap cell which is located on the neck-like protrusion of the basal cell. Both of the cap cell and the basal cell have dense cytoplasm, large nucleus, numerous mitoehondria and a few other organelles. The basal cell has wall protuberances, and infoldings of the partitioning membrane system which extend throughout the basal cell, and separate the basal cell cytoplasm. A dominant feature of the cap cell is the distinct compach, nueleolus and its chromatin distributed throughout the karyoplasm. In shoulder and bottom of the basal cell there is no cuticular layer separating them from the epidermal cell and mesophyll cells, but in the walls connceting the basal cell with the epidermal cells and cap cell there are pronounced plasmodesmata. It is possible that devolopment of the gland in Spartina anglica is the same as in S. townsendii, and that pathway of secretion is similar to both of S. foliosa and S. townsendii.     

Morphology of some polystichoid ferns

The morphology of the spores and prothalli of Arachniodes aristata, A. assamica, Cyrtomium caryotideum, C. falcatum and 10 species of Polystichum is described. The spores are bilateral with a smooth exine and the perine smooth in Cyrtomium and granulose to spinulose in the others. Spore germination is of the Vittaria type and prothallial development is of the Aspidium type. The adult prothallus of Arachniodes and Polystichum is cordate, with profuse papillate hairs. Sex organs are of the common leptosporangiate type. The antheridium dehisces by a pore-like opening in the cap cell in Polystichum , whereas the cap cell collapses at dehiscence in Arachniodes. Both species of Cyrtomium are apogamous; the thallus becomes irregular in shape in C. caryotideum but is cordate in C. falcatum.