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1.
紫苏腺毛的形态结构和发育的研究   总被引:2,自引:0,他引:2  
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。  相似文献   

2.
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。  相似文献   

3.
野薄荷叶腺毛的发育形态学研究   总被引:6,自引:1,他引:5  
研究了分布于我国东北部的野薄荷叶表面腺毛的结构和发育。主要腺毛有两种:多细胞盾状腺毛和弯曲单细胞头状腺毛。多细胞盾状腺毛由1个基细胞,1个柄细胞和一个由8-12个分泌细胞构成的头部组成。单细胞头状腺毛由1个基细胞,1个柄细胞和一个分泌细胞头部构成。  相似文献   

4.
冬凌草腺毛的形态学及组织化学研究   总被引:1,自引:0,他引:1  
利用光学显微镜对药用植物冬凌草地上部分腺毛的形态、分布和组织化学进行了研究。结果表明:(1)冬凌草的叶表皮有3种形态显著不同的毛,即非腺毛、盾状腺毛和头状腺毛;盾状腺毛和头状腺毛均具1个基细胞、1个柄细胞和头部;成熟的盾状腺毛的头部一般由4个分泌细胞组成,而头状腺毛头部由2个分泌细胞组成。(2)组织化学鉴定结果显示:2种腺毛中均含有黄酮类成分,盾状腺毛中还含有单萜、倍半萜等萜类成分;冬凌草甲素可能只存在于盾状腺毛中,但需要更直接的证据证明。研究认为,高密度的盾状腺毛可以作为筛选冬凌草高甲素含量品种的一项重要依据。  相似文献   

5.
羽叶薰衣草表皮毛的发育解剖学研究   总被引:1,自引:0,他引:1  
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。  相似文献   

6.
电镜观察表明:兰花鼠尾草(Salvia farinacea Benth.)的头状腺毛(capitate trichomes)和盾状腺毛(peltate trichomes)在超微结构方面存在明显不同,盾状腺毛的分泌细胞中占优势的细胞器是质体,而头状腺毛中是内质网和质体;成熟的盾状腺毛角质层下间隙明显,而头状腺毛不明显;盾状腺毛的柄细胞的侧壁出现完全的角质化现象,而头状腺毛则无;头状腺毛的基细胞液化程度比盾状腺毛的高。  相似文献   

7.
木香薷腺毛形态结构发生发育规律的研究   总被引:1,自引:0,他引:1  
采用常规石蜡切片法及扫描电镜技术对木香薷(Elsholtzia stauntoni Benth)腺毛发生发育及其规律进行了研究。结果表明:木香薷表皮上主要有两种表皮毛:无分泌细胞的表皮毛与有分泌细胞的腺毛。前者包括单细胞乳头状毛、2~3细胞管状毛、分枝状毛及多细胞管状毛;后者包括头状腺毛与盾状腺毛。成熟头状腺毛头部由1、2或4个分泌细胞构成,头部呈圆球形或半圆球形;成熟盾状腺毛头部由8~12个分泌细胞构成,分泌细胞横向扩展形成盾状头部。木香薷腺毛主要在茎端幼叶处大量发生,从茎端第一对幼叶处开始产生;从幼叶期到成熟期均有腺毛发生,大部分腺毛在幼叶期发生发育,只有极少部分在叶的成熟期进行发生发育。  相似文献   

8.
利用光学显微技术和扫描电镜技术,研究了香薷营养生长期和生殖生长期的枝条上部、中部、下部叶片的腺毛种类、分布及数量;采用组织化学染色和荧光显微技术,观察香薷腺毛分泌黄酮类物质的过程,探讨香薷叶表皮腺毛的泌香机理,为生产中确定提取香薷黄酮类物质的最佳取材时期提供依据。结果表明:(1)香薷叶表皮有头状腺毛和盾状腺毛,成熟的头状腺毛包括基细胞、柄细胞和头部,头部较小,呈半圆球型,直径为(20±2)μm;发育近成熟的盾状腺毛头部较大,呈盾状,直径为(60±5)μm。(2)香薷叶片远轴面和近轴面均有腺毛的分布,远轴面分布较多,近轴面分布较少;盾状腺毛主要分布在叶的远轴面,头状腺毛在叶的两面均有分布;腺毛密度随节位的降低而减少,节位相同时,营养生长期叶片上的腺毛密度(283.9个/mm2)高于生殖生长期(194.4个/mm2)。(3)香薷头状腺毛和盾状腺毛均能分泌黄酮类物质,且随着腺毛的发育成熟,黄酮类物质逐渐积累于腺毛的头部。  相似文献   

9.
紫苏腺毛的形态发生研究   总被引:4,自引:0,他引:4       下载免费PDF全文
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  相似文献   

10.
为了评价中药材溪黄草的三种基原——线纹香茶菜[Rabdosia lophanthoides(Buch.-Ham. ex D. Don)Hara]、纤花(细花)线纹香茶菜[Rabdosia lophanthoides var. graciliflora(Benth.)Hara]与溪黄草[Rabdosia serra(Maxim.)Hara]的安全性,采用SPF级昆明种(KM)小鼠分别灌服以上三种植物的提取物,对其急性毒性进行评价。三种植物提取物的最大给药剂量为每天每公斤300 g生药(约为临床人拟用剂量的1 154倍),随后连续观察14 d。结果显示,线纹香茶菜、纤花(细花)线纹香茶菜与溪黄草对小鼠体重、摄食量均无明显影响,给药组至试验结束时小鼠无死亡或明显的毒性反应。实验结果提示中药材溪黄草3种基原植物的安全性良好。  相似文献   

11.
This study characterises the micromorphology, ultrastructure and main chemical constituents of the foliar glandular trichomes of Ocimum obovatum using light and electron microscopy and a variety of histochemical tests. Two types of glandular trichomes occur on the leaves: large peltate and small capitate. The head of each peltate trichome is made up of four broad head cells in one layer. The head of each capitate trichome is composed of two broad head cells in one layer (type I) or a single oval head cell (type II, rare). In peltate heads, secretory materials are gradually transported to the subcuticular space via fracture in the four sutures at the connecting walls of the head cells. Release to the head periphery occurs through opposite fracture in the four sutures in the head cuticle. In type I capitate trichomes, release of the secretions to the subcuticular space occurs via a pore between the two head cells, and release to the head periphery occurs through the opposite pore in the head cuticle. In type II capitate trichomes, the secreted material is released from the head cell through a ruptured particular squared area at the central part of the head cuticle. These secretion modes are reported for the first time in the family Lamiaceae. Histochemical tests showed that the secretory materials in the glandular trichomes are mainly essential oils, lipophilic substances and polysaccharides. Large peltate trichomes contain a large quantity of these substances than the small capitate trichomes. Ultrastructural evidence suggests that the plastids produce numerous lipid droplets, and the numerous polysaccharide small vesicles are derived from Golgi bodies.  相似文献   

12.
The types of glandular trichomes, their ontogeny and patternof distribution on the vegetative and reproductive organs ofLeonotis leonurus at different stages of development, are studiedby light and scanning electron microscopy. Two morphologicallydistinct types of glandular trichomes (peltate and capitate)are described. Peltate trichomes, at the time of secretion,are characterized by a short stalk, which is connected witha large spherical head composed of eight cells in a single layer.Capitate trichomes can be divided into various types. Generally,they consist of a four-celled head supported by one or threestalk cells. The two kinds of trichomes differ in the secretionprocess. In the peltate trichomes, the secretory product seemsto remain accumulated in a subcuticular space, unless an externalfactor damages it. In the capitate trichomes, this product probablybecomes released through micropores. On the leaves peltate andcapitate trichomes are abundant, while on the flowers only thepeltate trichomes are numerous and the capitate are rare orabsent.Copyright 1995, 1999 Academic Press Leonotis leonurus R. Br., lion's ear, lion's tail, Lamiaceæ, glandular trichomes, morphology, ontogeny  相似文献   

13.
Leaves of Humulus lupulus possess two types of glandular trichomes: - peltate (lupulin) and bulbous.
Peltate trichomes are formed from a protodermal cell by two anticlinal divisions in perpendicular planes, followed by two periclinal ones that give rise to the initials of the head cells, the basal and the stalk cells. Head cells divide successively in radial and irregular planes. Fully developed peltate trichomes are built of a glandular head consisting of 30 to 72 cells, four stalk cells and four basal cells.
Bulbous trichomes are also formed from a protodermal cell by an anticlinal division followed by two periclinal ones that produce the initials of the glandular head cells, and the basal and stalk cells. Fully developed bulbous trichomes consist of four (occasionally eight) head glandular cells, two stalk cells and two basal cells.
The density of peltate trichomes decreases with the expansion of the leaves.
Both peltate and bulbous trichomes secrete essential oils. Peltate trichomes are the preferential site for the synthesis of bitter resins. Tannic acids could not be detected histochemically either in peltate or in bulbous trichomes. Both types of trichomes produce secretion that accumulates in the subcuticular space, being released, in the case of bulbous trichomes, by rupture of the cuticle.  相似文献   

14.
Ziziphora L. is represented by 5 species and 2 subspecies in the flora of Turkey: Z. clinopodioides, Z. capitata, Z. persica, Z. tenuior, Z. taurica subsp. taurica, Z. taurica subsp. cleonioides. It is difficult to distinguish between some Ziziphora taxa because of their morphological similarities. In this study, the leaf and calyx trichomes of Ziziphora taxa in Turkey were studied in order to assess anatomical variations that may serve as distinguishing characters. Their micromorphological features were surveyed by scanning electron microscopy (SEM) and light microscopy (LM). Trichomes on leaves and calyx can be divided into two general types: non‐glandular trichomes and glandular (secretory) trichomes. The non‐ glandular trichomes are simple, acicular or curved with cuticular micropapillae. They usually consist of one or more additional cells. The glandular trichomes are divided into two types: peltate and capitate and Ziziphora taxa can easily be distinguished by presence/absence, density and types of glandular trichomes on leaves and calyx. The peltate trichomes consist of 12 or 18 secretory head cells in a single disc; four or six central cells surrounded by eight or twelve peripheral ones. Peltate trichomes are absent on the adaxial leaf surface of Z. capitata and Z. persica. Two types of capitate trichomes are present in Ziziphora. The capitate trichomes are only absent on the calyx surface of Z. persica. In addition, the trichome micromorphology provides some support for separating the two subspecies of Z. taurica. In conclusion, Ziziphora taxa can easily be distinguished by cell number, cell shape presence/absence and density of the glandular trichomes on leaves and calyx.  相似文献   

15.
The genus Cyclotrichium (Boiss.) Manden. & Scheng. is represented by six species in Turkey: C. glabrescens, C. leucotrichum, C. longiflorum, C. niveum, C. origanifolium and C. stamineum. They are aromatic perennial subshrubs used as spices or herbal teas in traditional Turkish medicine. The leaf anatomy and tomentum morphology of leaves and calyces of Cyclotrichium species in Turkey was investigated by scanning electron microscopy (SEM) and light microscopy (LM). The investigated species have equifacial (C. niveum, C. origanifolium) or bifacial leaves (C. glabressens, C. leucotrichum, C. longiflorum, C. stamineum). All species have peltate and capitate glandular, and simple (all species) or branched (C. niveum) eglandular trichomes and diacytic stomata. Peltate trichomes consist of a basal cell embedded in the epidermis, a stalk cell, and a broad 12 (–13)‐celled secretory head arranged in two concentric circles. The capitate trichomes observed in Cyclotrichium can be grouped into five types, differing in structure and size. They consist of either a pear‐shaped or globose unicellular head and uni‐or bicellular stalk, or a bicellular head and bicellular stalk. The density of peltate, capitate and eglandular trichomes differs between species. Peltate trichomes are densely spaced only on the calyx and on the leaf surface of C. niveum and C. origanifolium and on the abaxial leaf surface of C. longiflorum and C. stamineum. The significance of trichome architecture for taxonomy in Cyclotrichium and Lamiaceae in general is discussed.  相似文献   

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