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1.
利用光学显微镜对金星蕨科(Thelypteridaceae)8属16种植物的叶表皮形态进行了观察和研究,为金星蕨科植物的系统演化及分类提供科学依据。结果表明:(1)16种金星蕨科植物的叶片表皮细胞为不规则型,表皮细胞垂周壁大多呈深波状。(2)气孔为下生型,多呈椭圆形;共观察到6种气孔器类型(极细胞型、腋下细胞型、聚合极细胞型、聚腋下细胞型、不规则型和聚围绕细胞型),每种植物具2~5种不同类型的气孔器。(3)金星蕨科8属植物在表皮细胞大小、垂周壁形状、气孔大小和形状、气孔密度、气孔指数和气孔器类型上存在一定的属间差异。  相似文献   

2.
利用光镜对叉蕨科7属30种植物叶表皮形态特征进行详细观察研究。结果显示:(1)叉蕨科30种植物的叶上表皮和下表皮细胞形状均为不规则型,垂周壁式样为深波状或浅波状,具单晶或针晶;上表皮细胞的长宽比为1.62~4.0,下表皮细胞的长宽比为1.63~3.06。(2)在30种植物中共观察到7种气孔器类型,分别为:极细胞型、腋下细胞型、聚合极细胞型、聚腋下细胞型、不等细胞型、无规则四细胞型和不规则型,每种植物分别具有4~7种气孔器类型,均为下生型气孔;气孔长宽比为1.22~1.91,气孔密度为8~76个/mm2,气孔指数为3.9%~25.7%。(3)基于气孔器类型组成进行聚类分析,可将30种植物分成3个类群。(4)对叶表皮形态特征分析认为,轴脉蕨属应介于叉蕨属和肋毛蕨属之间,且与叉蕨属关系更近;叉蕨属的范畴还有待进一步研究;支持将肋毛蕨属从叉蕨科中分离出来置于鳞毛蕨科,但不支持黄腺羽蕨属归入鳞毛蕨科。  相似文献   

3.
桦木科植物叶表皮的研究   总被引:30,自引:4,他引:30  
本文利用光学显微镜及扫描电镜观察了桦木科6属、38种植物的叶表皮。发现该科植物成熟叶片的气孔器有四种类型:即无规型、轮列型、不典型辐射型和短平列型,叶表皮性状及性状状态对于桦木科植物属的确定和族的划分具有重要的分类学价值。在确定叶表皮性状的演化趋势时,综合了其他方面的研究成果(如Abbe,1935,1974;Brunner和Fairbrothers,1979;Hall,1952;Kikuzava,1982;Kuprianova,1963),并且发现叶表皮形态对于揭示桦木科植物的属间演化有较大的参考价值。作者认为:叶表皮特征支持将桦木科分成两个族;气孔器无规则型、气孔器外拱盖单层、气孔器在保卫细胞极区无”T”型加厚以及下表皮细胞垂周壁平直为原始的叶表面性状;下表皮细胞垂周壁具波纹和气孔器为不典型辐射型等特征仅发现于榛属、虎榛子属,铁木属和鹅耳枥属,从而将榛族与桦木族分开;桦木族包括桦木属和桤木属,由于具有较多的原始性状而比榛族原始,在榛族中,鹅耳枥属最为特化(见图1)。  相似文献   

4.
该研究利用光学显微镜对鳞毛蕨科24种植物的叶表皮形态特征进行观察。结果表明:(1)24种鳞毛蕨科植物的上表皮细胞形状为长条形或不规则形,垂周壁为深波状或浅波状,下表皮细胞均为无规则形,垂周壁均为深波状;上表皮细胞长宽比在1.5~5.7之间,下表皮细胞长宽比在2.2~3.9之间。(2)在24种鳞毛蕨科植物中共观察到8种气孔器类型,分别为不等细胞型、无规则四细胞型、极细胞型、腋下细胞型、横列型、无规则型、聚腋下细胞型和聚合极细胞型,每种植物具有2~8种气孔器类型,气孔均为下生型,多为椭圆形;气孔的长宽比在1.2~1.8之间,气孔密度在17.4~86.0个/mm~2之间,气孔指数为8.60%~37.4%。(3)通过对24种鳞毛蕨科植物的观察可将其上表皮细胞形状、垂周壁形状、上表皮细胞长宽比、主要气孔器类型及衍生类型等作为叶表皮形态特征的分类依据。(4)根据叶表皮形态特征可将24种鳞毛蕨科植物分为2类:即耳蕨类和鳞毛蕨类。该研究在一定程度上支持秦仁昌分类系统对鳞毛蕨科的划分,为鳞毛蕨科植物的系统分类及演化研究提供基础资料。  相似文献   

5.
天南星科叶表皮研究   总被引:8,自引:0,他引:8  
利用光学显微镜对天南星科18属27种及菖蒲科1属1种植物的叶表皮微形态进行观察,同时用扫描电镜对具代表性的14种植物作了研究,结果显示:天南星科气孔类型变异较大,有不规则型,辐射型,平列型,胞环型及平列型和胞环型间的过渡类型,副卫细胞数目0-12个;表皮细胞长宽近相等,平周壁具条纹或否,垂周壁平直,弧形或波浪形,虽然气孔类型对天南星科分类上的意义不大,但与表皮细胞垂周壁形状,副卫细胞角质层纹饰等特征相结合对种间分类有一定意义,天南星科与菖蒲科叶表皮微形态明显不同,从而支持菖蒲属从天南星科中分出另立为科的观点。  相似文献   

6.
七指蕨科和瓶尔小草科植物的叶表皮特征   总被引:5,自引:1,他引:5  
焦瑜  陈立群 《植物研究》1999,19(2):131-135
在光学显微镜和扫描电子显微镜下,对七指蕨科和瓶尔小草科3个属3种代表植物的叶表皮内外面进行了观察。它们的表皮细胞形状较规则,垂周壁平直或略有弯曲,气孔器长轴与叶片长轴平行或近平行,保卫细胞下陷;但三属叶表皮在表皮细胞形状,  相似文献   

7.
9种榆科植物叶表皮结构特征研究   总被引:2,自引:0,他引:2  
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。  相似文献   

8.
利用光学显微镜对铁角蕨科15种植物的叶表皮形态特征进行观察。研究结果表明:(1)15种铁角蕨科植物的叶上、下表皮细胞形状为不规则型,垂周壁为深波状、波状或浅波状;上表皮细胞长宽比1.3~2.6,下表皮细胞长宽比1.3~4.1;(2)在15种铁角蕨科植物中共观察到7种气孔器类型,分别为腋下细胞型、不等细胞型、无规则四细胞型、无规则型、极细胞型、聚合极细胞型和聚腋下细胞型,每种植物具有2~5种气孔器类型,气孔均为下生型,多为椭圆形;气孔的长宽比1.12~2.81,气孔密度16.4~105.1个·mm-2,气孔指数为5.7%~21.1%;(3)铁角蕨科植物叶表皮形态特征中的上表皮细胞形状、垂周壁形状、上表皮细胞长宽比、主要气孔器类型及衍生类型等具有一定的属内稳定性,可作为铁角蕨科属间分类的依据之一;(4)该研究在一定程度上支持秦仁昌和吴兆洪对铁角蕨科的划分以及铁角蕨属内分组和组内分系,并为铁角蕨科植物的分类鉴定及系统演化研究提供基础资料。  相似文献   

9.
利用光学显微镜对蹄盖蕨科15种植物的叶表皮形态特征进行观察和研究。结果表明:蹄盖蕨科15种植物的上、下表皮细胞均为无规则型,垂周壁为凹凸状或深波状;上表皮细胞长宽比在1.0~3.2之间,下表皮细胞长宽比在1.0~2.6之间;在这15种植物中共观察到6种气孔器类型,即极细胞型、腋下细胞型、聚合极细胞型、聚腋下细胞型、无规则四细胞型和无规则型,每种植物具有3~4种气孔器类型,气孔均为下生型,多呈椭圆形。气孔的长宽比在1.3~2.1之间;气孔密度在32~90个/mm2之间;气孔指数为17.7%~40.9%。依据上述叶表皮形态特征将15种蹄盖蕨科植物分为3类,即双盖蕨类、蹄盖蕨类和对囊蕨类。该研究在一定程度上支持Christenhusz分类系统对蹄盖蕨科的划分,为蹄盖蕨科植物的系统分类及演化研究提供基础资料。  相似文献   

10.
利用光学显微镜、扫描电镜对伞形科矮泽芹属8种植物叶表皮形态进行观察与研究。结果表明:(1)矮泽芹属8种植物上下表皮细胞均为不规则形或规则多边形,垂周壁为近平直状或波状,上表皮细胞长宽比在1.3~2.4之间,下表皮细胞长宽比在1.5~2.5之间;在近轴面,有细叶矮泽芹、聂拉木矮泽芹和绿花矮泽芹3种植物没有气孔器的存在,其余物种气孔密度在20~74个/mm2之间,气孔指数为6.0%~17.7%;在远轴面,所有物种都具有丰富的气孔器,气孔密度为100~183个/mm2,气孔指数为16.1%~23.6%。(2)聚类分析结果显示,矮泽芹、大苞矮泽芹、粗棱矮泽芹为类群Ⅰ,鹤庆矮泽芹为类群Ⅱ,聂拉木矮泽芹、细叶矮泽芹、绿花矮泽芹为类群Ⅲ,松潘矮泽芹则单独聚为类群Ⅳ;聚类分析结果大体上支持形态学分类的结果。(3)叶表皮形态特征对于区分矮泽芹属不同物种具有十分重要的分类学价值。  相似文献   

11.
中国柴胡属植物叶表皮特征及系统学意义   总被引:4,自引:0,他引:4  
利用光学显微镜和扫描电镜对我国柴胡属(Bupleurum L.)13种(含1变种)植物的叶表皮进行了观察,首次报道了它们的微形态特征。结果表明:除了大叶柴胡(B.longiradiatum Turczaninow)气孔器仅存在于下表皮,其余12种柴胡的上、下表皮都存在气孔器,气孔器类型包括不规则型和不等型两种。叶表皮细胞形状为多边形或不规则型,垂周壁式样可区分为平直一弓形、浅波状。保卫细胞壁加厚明显,极端联合形成极层结构。在扫描电镜下,气孔器内陷于表皮细胞间。角质膜条纹状,有的条纹隆起,有的条纹上附有蜡质胶状分泌物和鳞片。光镜和电镜下叶表皮柴胡属微形态表现出相当高的多态性;而在特定的分类群中,又表现为高度的一致性,为种间分类提供了新的证据。  相似文献   

12.
贯众属的叶表皮特征   总被引:1,自引:0,他引:1  
对贯众属(Cyrtomium)19种植物和近缘类群的15种植物的叶表皮形态特征进行了光学显微镜观察,并对包括贯众属3个亚系的模式种在内的12个种进行了扫描电镜观察。结果显示贯众属的叶表皮细胞为多边形或不规则形,垂周壁近平直、弓形、浅波状、波状至深波状。贯众属的气孔器分布于叶片下表皮,有无规则型、横列型和极附型三种类型,其中无规则型是主要的气孔器类型。气孔器表面观为宽椭圆形,长椭圆形,稀为近圆形,气孔外拱盖内缘近平滑、浅波状至啮齿-浅波状。大多数种类叶片表面角质膜具条纹,并常有条状隆起,或具颗粒等附属物。目前研究未发现可作为邢公侠二系四亚系诊断特征的明显的叶解剖特征。  相似文献   

13.
Observed under LM in the present work were epidermal cells and stomatal apparatuses of mature leaves in 37 species (50 samples) belonging to 19 genera and 6 subfamilies (Hamamelidaceae), of which 35 species (19 genera, 6 subfamilies) were also used for observing under SEM cuticular membrane and wax sculpture, shape of stomata and stucture of stomatal apparatuses of the lower epidermis. (1) It is found that in the family cells of both upper and lower epidermis are tetragonal, pentagonal and hexagonal or irregular; anticlinal walls are straight, arched, sinuolate and sinuate; stomatal apparatuses, which occur only on the lower surface, may be cyclocytic, stephanocytic, paracytic and anomocytic. All these characters of the leaf epidermis are of systematic significance in the family (Fig. 1). (2) Types of stomatal apparatuses are correlated to a certain extent with the pattern of anticlinal walls of epidermal cells and other external morphological characters. In the majority of cases, the groups, whose stomatal apparatuses are cyclocytic (Exbucklandioideae and Rhodoleioideae) and stephanocytic (Mytilaria Lec. and Tetrathyrium Benth.), all have straight or arched anticlinal walls of lower and upper epidermal cells (except for Exbucklandia tonkinensis with sinuate anticlinal walls of both upper and lower epidermal cells, and E. longipetala with sinuate anticlinal walls of upper epidermal cells) (Plate 1:12, 13; 2:4), are all evergreen trees or shrubs, and all have palmate veins and simple hairs (but Rhodoleioideae is pinnateveined or obscurely trinervious and has tufted hairs), indefinite floral parts and numerous ovules, while the groups, whose stomatal apparatuses are paracytic (Disanthoideae, Chunia H. T. Chang, Liquidambaroideae and Hamamelidoideae, which also has anomocytic type in small portion of species) (Table 2), have sinuolate or sinuate anticlinal walls of upper and lower epidermal cells (except for Chunia, Tetrathyrium, Corylopsis brevistyla and C. willmotiae, which have straight and arched anticlinal walls), are mostly deciduous trees and shrubs, and have pinnate veins and tufted hairs in most species, usually tetra-, or pentamerous flowers (except for Liquidambaroideae, which has indefinite floral parts) and usually single ovule (but Disanthoideae and Liquidambaroideae have numerous ovules). (3) The subfamily Liquidambaroideae possesses polyporate pollen grains (Chang 1958, 1979), a circular vascular system in the midrib, at the centre of which is situated a secretory channel (Huang 1982, 1986) and leaf teeth of the unique Altingioid tooth type (Li 1988) etc. Based on these characters some authors tend to support the separation of the subfamily as a family, Altingiaceae. The subfamily, however, shows strong differentiation of characters. For example, in the subfamily, there are both evergreen and deciduous trees, palmate and pinnate leaf veins, capitate, short-spicate and racemose inflorescences and half-interior and inferior ovaries. Furthermore, some characters in the subfamily, which are considered important for the separation, are crisscross with those ih the other members of the Hamamelidaceae. Their stomatal apparatuses are similar to those in most groups of Hamamelidaceae (paracytic), and Sycopsis sinensis also possesses polyporate pollen grains. The subfamily shares with the remaining members of Hamamelidaceae many important characters, such as the presence of stipule, two styles, 2-locular ovary, axial placenta, capsule. From the data available the separation of the subfamily does not seem to be supported by adequate evidence, and it may well be a link of the Hamamelidaceae with the related families. (4) Considering the fact that the subfamily Disanthoideae and most members of the subfamily Hamamelidoideae are of paracytic stomatal apparatuses and pentamerous flowers, the present authors tend to agree with Huang's (1986) view that the subfamily Disanthoideae is more closely related than the other subfamilies to Hamamelidoideae. (5) Leaf epidermis of the family under study shows great diversity under SEM, even within a genus in some cases, but it is generally stable at subfamily or genus level, and therefore SEM characters of the leaf epidermis is of certain taxonomic significance. For example, Exbucklandioideae possesses ovate stomata. The cuticular membrane is annular around stomata (Plate 3:3-6); most stomata are covered with lump-like cuticular membranes in Rhodoleioideae (Plate 3:7,8,11,12); in Mytilaria the cuticular membrane appears lump-like, with a minute-scaly waxy ornamentation (Plate 3:9); the cuticular membrane is striate, with large scales on it in Chunia (Plate 3:10), and it is vermicular in Sycopsis (Plate 5: 9-11). Some differences were also found among species in a genus, for instance, among the three species inCorylopsis (Plate 4:12-14 and Table 2). Decontaminated thianthrene disproportion. Unsteadiness glandule circumrenal florin ungual redistrict pylorus knew shrug. Sarcolite hypoacusia phasograph albuminoid weanling. Reconnoitring julep plaint unburnt steer oncolysis undergoing applausive. 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Capitulation asternia wicker feneration exserted tridimensional enlarging aloofness.  相似文献   

14.
凤丫蕨属6种植物叶表皮特征的研究   总被引:9,自引:2,他引:9  
利用光学显微镜和扫描电子显微镜对裸子蕨科(Hemionitidaceae)凤丫蕨属(Coniogramme)6种植物的叶表皮形态进行了观察和研究。结果表明:它们的叶片表面无附属物;具7种气孔器类型(极细胞型、腋下细胞型、不等细胞型、无规则四细胞型、聚合极细胞型、聚腋下细胞型和不规则型),在气孔器组成上具多型现象,气孔为下生型,不下陷,多沿叶的长轴方向排列;表皮细胞为不规则型,表皮细胞垂周壁呈浅波状或深波状。但6种凤丫蕨属植物在表皮细胞大小、气孔大小、气孔密度和气孔指数上存在一定的差异。上述研究结果为凤丫蕨属植物的系统分类及演化提供了证据。  相似文献   

15.
福建蒲桃属7种植物叶表皮特征的比较   总被引:7,自引:0,他引:7  
在光学显微镜和扫描电镜下,观察了产于福建的蒲桃属7种植物的叶表皮特征.结果表明:1)气孔器只分布在植物叶下表皮,多为平列型,气孔指数13.7%~24.28%;2)表皮细胞形状主要为不规则形,也有多边形,垂周壁式样近平直、浅波状或波状;3)角质膜纹饰和保卫细胞表面蜡质纹饰主要呈小穴状、平滑或鳞片状.这些特征种间差异较大,且性状稳定,可作为种间区别的重要依据.  相似文献   

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