无距虾脊兰营养器官解剖结构及其生态适应性

采用石蜡切片法对无距虾脊兰（Calanthe tsoongiana T.Tang et F.T.Wang）营养器官解剖结构进行研究。结果显示,无距虾脊兰叶为等面叶,与一般植物相比,表皮毛和气孔器较少,均分布在下表皮,气孔器稍外凸,叶片维管束分化程度不一,木质部厚度远大于韧皮部。假鳞茎由表皮、基本组织和维管束组成,基本组织发达,含有丰富的内含物。维管束散生于基本组织中;根主要由根被、皮层和中柱组成,根被通常可见4层,皮层由8~10层薄壁细胞组成,菌丝体通过破坏根被细胞侵入皮层。除正对木质部脊的中柱鞘细胞外,其余中柱鞘通道细胞全面增厚,维管束类型为辐射维管束,中柱中央为薄壁细胞组成的髓。无距虾脊兰营养器官的解剖特征表现出阴生植物的特点,引种栽培过程中应注意适当遮荫和通风。     

无距虾脊兰营养器官解剖结构及其生态适应性

采用石蜡切片法对无距虾脊兰(Calanthe tsoongiana T.TangetF.T.Wang)营养器官解剖结构进行研究。结果显示,无距虾脊兰叶为等面叶,与一般植物相比,表皮毛和气孔器较少,均分布在下表皮,气孔器稍外凸,叶片维管束分化程度不一,木质部厚度远大于韧皮部。假鳞茎由表皮、基本组织和维管束组成,基本组织发达,含有丰富的内含物。维管束散生于基本组织中;根主要由根被、皮层和中柱组成,根被通常可见4层,皮层由8~10层薄壁细胞组成,菌丝体通过破坏根被细胞侵入皮层。除正对木质部脊的中柱鞘细胞外,其余中柱鞘通道细胞全面增厚,维管束类型为辐射维管束,中柱中央为薄壁细胞组成的髓。无距虾脊兰营养器官的解剖特征表现出阴生植物的特点,引种栽培过程中应注意适当遮荫和通风。     

虉草营养器官解剖结构与抗旱耐涝性及利用之间的关系

为了从显微结构上进一步探讨虉草(Phalaris arundinacea L.)的抗旱耐涝性及与利用的关系,于2011年采用常规石蜡切片技术,对其根、茎叶3种营养器官进行解剖观察。结果表明,虉草根的结构自外而内依次为表皮、皮层、维管束鞘、初生韧皮部和初生木质部;茎由表皮、基本组织和维管束构成;叶片内部结构可分为表皮、叶肉和叶脉3部分。根皮层大的细胞间隙和气腔,初生木质部的后生大导管和茎基本组织解体形成的髓腔都是虉草良好的通气组织,是其耐水淹的主要显微特征。茎、叶片角质化的表皮和叶表皮所含的丰富泡状细胞组是虉草具有抗旱性的主要解剖结构特征。叶肉细胞排列紧密且只有少量气孔分布于叶片下表皮,这样的结构可减少蒸腾;叶肉细胞富含叶绿体,增强光合作用,获得更多的同化产物,确保了植株在干旱条件下也有足够的光合产物来维持正常的生理活动。茎、叶维管束部分大量的木纤维起到支撑作用。虉草根的皮层和维管柱部分、茎的基本组织和维管束部分、叶的叶脉部分都含有大面积的厚壁细胞,厚壁细胞中含有丰富的粗纤维和木质素。丰富的粗纤维、木质素等成分则是虉草能成为新能源燃料植物的必备条件。     

蒙古黄芪营养器官的解剖结构研究

通过对蒙古黄芪营养器官解剖结构研究表明,根为典型的双子叶植物根的结构,初生结构由表皮、皮层和维管柱组成,初生木质部和初生韧皮部在分化过程中呈外始式,初生木质部四原型,皮层内具凯氏带;茎由表皮、皮层和维管柱组成,维管束为外韧无限维管束;叶为异面叶,由表皮、叶内和叶脉组成,栅栏组织排列紧密且整齐,细胞呈长柱形,海绵组织排列疏松且不整齐,细胞呈海绵状,有大量气隙,叶脉维管束发达,为外韧无限维管束,叶上下表皮均具有气孔.     

碱蒿营养器官的扫描电镜观察研究

用扫描电子显微镜对碱蒿（Artemisia anethifolia）营养器官的解剖学特征进行了观察与研究。结果表明：碱蒿属于典型的泌盐盐生植物。叶肉质化,表皮上气孔为无规则型气孔,密集下陷,有较多的盐囊泡和分杈腺毛分布,表皮细胞外壁加厚,外壁的外层角质化,为等面叶,栅栏组织细胞排列疏松,叶中央为发达的储水组织,木质部有多束维管束;茎表皮上有少许气孔,并分布有腺毛和众多盐囊泡,表皮细胞外壁加厚形成角质层,皮层宽度较小,皮层薄壁组织细胞内可见淀粉粒,中柱后生木质部为口径大的导管,原生木质部为口径小的导管,管内充满盐晶体,中间有发达的贮水薄壁细胞;根的表皮细胞排列疏松,外皮层细胞排列紧密而整齐,中部皮层薄壁细胞层数较多,细胞中贮藏有许多淀粉粒,内皮层细胞排列紧密,初生木质部导管发达,内部周围存在大量盐晶体,根的次生木质部有通气组织。这些解剖结构均表现出碱蒿具有适应盐碱、干旱生境的结构特征。     

铁筷子(毛茛科)营养器官的结构及其系统学意义

应用解剖学方法,对铁筷子(Helleborus thibetanusFranch.)(毛茛科)营养器官的结构进行了研究。结果表明,铁筷子根的初生结构观察到三原型、四原型和六原型。营养器官中的维管束在横切面上木质部中的导管分子不呈“V”字形排列;根状茎的次生结构由外向内为表皮、皮层和维管柱,髓射线发达。茎的初生结构中多个维管束排列成环状,维管束鞘分化不明显,节部为单隙三迹,叶迹分别来自于3条维管束或同一条维管束。叶为两面叶,表皮细胞不规则;气孔器只分布于下表皮,为毛茛科典型的无规则型气孔。从铁筷子营养器官的解剖学特点来看,与毛茛科其它植物基本相同,但在营养器官中维管束木质部不呈“V”字形、维管束鞘分化不明显、节部具单叶隙等特征上与其它毛茛科植物不同。     

桃儿七营养器官解剖结构的地理差异

运用植物解剖学技术对云南、四川、甘肃和宁夏等6个居群桃儿七(Sinopodophyllum emodi)营养器官的结构进行了比较研究.结果显示,(1)桃儿七为多年生草本,根状茎发达,其次生结构包括周皮、皮层和维管组织三部分.(2)各居群间的差异主要表现在木栓层厚度、维管束个数和大小、导管分布格局以及淀粉粒的分布位置.其中:根初生结构由表皮、皮层和中柱构成,各居群间的差异主要表现在皮层厚度、初生木质部类型以及淀粉粒的分布位置;茎由表皮、皮层和维管柱构成,维管束均为外韧型维管束,仅具束中形成层,髓维管束与正常维管束之间形成腔隙,差异主要表现在基本组织厚度、维管束数量及大小.(4)桃儿七叶片构造类似于一般双子叶植物,由表皮、叶肉、叶脉三部分构成,下表皮气孔较多且孔下室发达,差异主要表现在叶片厚度等方面.研究表明,桃儿七营养器官的结构既表现出一定的耐旱性,又与阴生环境相适应,各居群的结构特点与其分布区生态环境密切相关.     

贵州北盘江喀斯特地区6种兰科植物结构及其生态适应性

【目的】分析兰科植物营养器官结构对喀斯特生境的适应特性和不同兰科植物响应生境异质的生存策略,为兰科植物研究、保护与发展提供理论支持和参考依据。【方法】该研究以贵州北盘江喀斯特地区6种不同生活型兰科植物的叶、假鳞茎、根为研究对象。应用石蜡切片法,进行结构观察并测量相关指标,通过描述和方差分析、相关性分析和主成分分析。【结果】结果表明：(1)不同兰科植物结构特征间存在显著差异,丘北冬蕙兰、莎叶兰、兔耳兰和单叶石仙桃均为等面叶,叶片较薄;栗鳞贝母兰与梳帽卷瓣兰叶片为异面叶,有栅栏组织和海绵组织的分化,叶片较厚。(2)假鳞茎主要由表皮、基本组织和维管束组成,地生兰基本组织细胞较小,维管束密度大;附生兰基本组织细胞较大,储水结构较发达。(3)地生兰根被和皮层较厚,根被细胞排列紧密,皮层细胞小层数多;附生兰根被与皮层较薄,皮层细胞较大。(4)叶片下表皮厚度与叶片厚度、叶维管束直径、叶肉厚度、叶脉厚度呈极显著(?<0.01)正相关,叶肉厚度与下角质层厚度、茎维管束直径呈显著(?<0.05)负相关;茎直径和表皮厚度、茎维管束数量、茎横截面积呈极显著正相关,茎维管束直径占比与茎直径、表皮厚度、茎维管束数量、茎横截面积均呈极显著负相关;根的各指标间呈极显著正相关,根直径、根被厚度和皮层厚度与根维管束直径占比呈极显著负相关。【结论】兰科植物根部结构具有相对稳定的趋同适应性,叶片和假鳞茎结构间相互促进协调,是兰科植物响应干旱喀斯特环境的重要结构。 关键词 生态适应性;兰科植物;结构特征;喀斯特地区     

墨兰的解剖学研究

运用石蜡切片法和扫描电镜技术,对墨兰营养器官和生殖器官进行了研究。结果表明墨兰叶片表面具较厚的角质层。气孔多为四轮列型,分布在下表皮,叶肉没有海绵组织和栅栏组织的分化,但叶尖部和叶中部中脉附近的叶肉细胞常伸长,类似栅栏组织细胞,平行脉,外韧型维管束,在假鳞茎中,维管束散生在基本组织中,根具根被,皮层和维管柱三部分,花被各部分基本结构均相似,唇瓣和合蕊柱的表皮为腺表皮,具花柱道,三心皮雌蕊,一室,侧膜胎座,四合花粉,表面无纹饰,蒴果。     

濒危植物革苞菊营养器官的解剖学研究

革苞菊为菊科多年生强旱生草本植物,是蒙古高原植物区系的特有种。本文通过常规石蜡切片法,对革苞菊营养器官进行了形态结构的观察。结果表明：革苞菊叶为等面叶,表皮由1层排列紧密的细胞组成,上下表皮均具气孔,为不规则形;栅栏组织位于上下表皮的内侧,由1层细胞组成;海绵组织由2~3层细胞构成,细胞排列疏松。茎为外韧维管束,可分为表皮、皮层和维管柱三部分,髓发达,髓射线为4~6列细胞。根可分为周皮、皮层、维管柱三部分,根中无髓,导管由中心向四周呈束状辐射排列。在茎与根的薄壁组织中分布着排列整齐的分泌结构。用PAS反应鉴定多糖、考马斯亮蓝鉴定蛋白质后观察了革苞菊的根茎叶中蛋白质和多糖的分布。本文同时讨论了革苞菊营养器官的内部构造与其所处生态环境相适应的特性。     

Anatomy of vegetative organs,inflorescence axis and pedicel in the Neoregelia bahiana complex (Bromeliaceae): taxonomic and ecological importance

Delimitation of genera and species in Bromeliaceae is often problematic, for example in the Neoregelia bahiana complex which is distributed throughout the rocky fields of the Espinhaço Range, Brazil. Considering that the anatomical characterisation of different organs is potentially important for taxonomic and ecological interpretation of this complex, we analysed roots, stems (stolon), leaves, inflorescence axes (peduncle) and pedicels in individuals from different populations. In all the studied individuals, the roots are composed of velamen, a heterogeneous cortex, and a polyarch vascular cylinder with sclerenchymatous pith. The stolon features a parenchymatous cortex and collateral vascular bundles randomly distributed in the vascular cylinder. This organ may increase in diameter by the formation of new vascular bundles and a multi‐layered cork. The leaf blade has epidermal cells with U‐shaped thickened walls and peltate scales occur on the adaxial surface. The mesophyll consists of mechanical and water‐storage hypodermis and a heterogeneous chlorenchyma. The inflorescence axis and the pedicel have a parenchymatous cortex and vascular bundles randomly distributed in an aerenchyma. Some variable leaf characters, such as presence of air lacunae in the mesophyll, are related to the size of the individuals and were interpreted as phenotypic variations related mainly to sunlight incidence. In contrast, leaf characters such as lamina shape, distribution of the peltate scales, and number of cell layers forming the water‐storage hypodermis distinguish the populations of the Serra do Cabral and one population of the Diamantina (Minas Gerais) from the remaining studied populations, suggesting the existence of more than one taxon.     

THE RELATIONSHIP BETWEEN THE PRIMARY THICKENING MERISTEM AND THE SECONDARY THICKENING MERISTEM IN YUCCA WHIPPLEI TORR. I. HISTOLOGY OF THE MATURE VEGETATIVE STEM

Anatomical observations were made on 1-, 2-, and 3-yr-old plants of Yucca whipplei Torr, ssp. percursa Haines grown from seed collected from a single parent in Refugio Canyon, Santa Barbara, California. The primary body of the vegetative stem consists of cortex and central cylinder with a central pith. Parenchyma cells in the ground tissue are arranged in anticlinal cell files continuous from beneath the leaf bases, through the cortex and central cylinder to the pith. Individual vascular bundles in the primary body have a collateral arrangement of xylem and phloem. The parenchyma cells of the ground tissue of the secondary body are also arranged in files continuous with those of the primary parenchyma. Secondary vascular bundles have an amphivasal arrangement and an undulating path with frequent anastomoses. Primary and secondary vascular bundles are longitudinally continuous. The primary thickening meristem (PTM) is longitudinally continuous with the secondary thickening meristem (STM). Axillary buds initiated during primary growth were observed in the leaf axils. The STM becomes more active prior to and during root initiation. Layers of secondary vascular bundles are associated with root formation.     

海南龙血树的形态组织学研究

采用植物解剖学、显微切片技术等,分别对海南龙血树含有树脂的茎、不含树脂的茎、幼根和叶片等进行了系统的组织学研究。结果表明：老茎主要由栓化层、皮层、形成层和基本组织4部分组成,树脂主要分布在基本组织内维管束的导管和纤维中。叶片为等面叶,气孔主要分布在下表皮上、具有明显的孔下室,上下表皮内侧分布着大量的纤维束。幼根由根被细胞、皮层和维管柱组成。根、茎、叶的部分薄壁细胞中均含有晶束。海南龙血树营养器官的结构特征与干旱、高温和贫瘠的生态环境相适应。这些结果可为海南龙血树的开发和利用提供基本的解剖学证据。     

喀斯特地区莎叶兰的解剖构造及其环境适应性

以广西西北部雅长兰科植物保护区的莎叶兰( Cymbidium cyperifolium)为对象,采用石蜡切片法对莎叶兰叶片和根的解剖构造及其对喀斯特环境的适应性进行了研究。结果表明：(1)莎叶兰叶片的上表皮覆盖有较厚的角质层,气孔均分布于下表皮,且凸出表皮细胞之上;各表皮性状在叶片不同部位存在显著差异,叶片下部的气孔密度、气孔指数和气孔长度最大,表皮细胞密度以叶片上部的最大;叶片属于等面叶,叶肉无栅栏组织和海绵组织的分化;叶脉为明显的平行脉,且粗细交互分布;(2)莎叶兰根的横切面包括根被、皮层、中柱3部分,其中根被细胞排列紧密,为生活细胞;皮层由薄壁细胞组成;根部维管束属于辐射维管束,14原型。菌根粗壮,稀根毛,共生真菌主要分布于根被及皮层中,菌丝体通过根被薄壁细胞间隙及内、外皮层的通道细胞进行侵染。(3)莎叶兰叶片和根的结构不仅有湿生植物特征,如叶片相对较薄、气孔少且凸出表皮细胞、冠/根比值大等;还有旱生植物的特征,如叶片角质层较厚、机械组织发达、细胞结构紧密、具含晶细胞,肉质根具根被,内、外皮层细胞壁明显增厚等。这些结构是莎叶兰对当地缺水、干湿季明显、分布于林下多石砾土壤的生长环境的一种高度适应性表现。     

波温苏铁(Bowenia spectabilis)营养器官的解剖结构研究

报道了波温苏铁Bowenia spectabilis Hook.ex Hook. f）根、茎、叶的解剖结构.根的初生结构由表皮、皮层和中柱三部分组成,为二原型木质部.茎具大量薄壁组织,薄壁细胞富含淀粉粒,维管束为外韧并生.叶柄中含有5-8束维管束,呈弧形排列.羽片叶角质层厚,有小叶脉产生,气孔主要分布在下表皮.根、茎、叶木质部中的管胞主要是螺纹和孔纹管胞,有少量纤维分化;茎中管胞的侧壁呈现凹凸不平,部分管胞具有分枝或分叉现象.     

Cellular compartmentation of ammonium assimilation in rice and barley

This review describes immunolocalization studies of the tissue and cellular location of glutamine synthetase (GS; EC 6.3.1.2) and glutamate synthase (Fd GOGAT; EC 1.4.7.1 and NADH-GOGAT; EC 1.4.1.14) proteins in roots and leaves of rice (Oryza sativa L.) and barley (Hordeum vulgare L.). In rice, cytosolic GS (GS1) protein was distributed homogeneously through all cells of the root. NADH GOGAT protein was strongly induced and its cellular location altered by ammonium treatment, becoming concentrated within the epidermal and exodermal cells. Fd GOGAT protein location changed with root development, from a widespread distribution in young cells to becoming concentrated within the central cylinder as cells matured. Plastid GS protein was barely detectable in rice roots, but was the major isoform in leaves, being present in the mesophyll and parenchyma sheath cells. GS1 was specific to the vascular bundle, as was NADH GOGAT, whereas Fd GOGAT was primarily found in mesophyll cells. In barley roots, GS1 protein was found in the cortical and vascular parenchyma and its concentration was highest in N-deficient seedlings. Plastid GS protein was detected in both cortical and vascular cells, where different plastid forms, containing different concentrations of GS protein, were identified. In barley leaves, GS2 protein was detected in the mesophyll chloroplasts and GS1 was found in the mesophyll and vascular cells. N nutrition strongly influenced this distribution, with a marked increase in GS1 concentration in the vascular cells in response to nitrate and ammonium, and an increase in mesophyll GS2 concentration in nitrate-grown seedlings. Fd GOGAT protein was found in both the mesophyll and vascular plastids. These localization studies show that the GS/GOGAT cycle is highly compartmentalized at both the subcellular and cellular levels. Reasons for this compartmentation, and the roles of each isoform, are discussed.