Comparative anatomy and systematics of Catasetinae (Orchidaceae)

Catasetinae consist of five genera of pseudobulbous Orchidaceae of the Neotropics. Anatomy is characterized by sunken, three-celled foliar hairs, mostly tetracytic stomatal apparatuses, superficial stomata, homogeneous mesophyll, foliar fibre bundles, collateral vascular bundles in a single row, xylem and phloem sclerenchyma associated with vascular bundles in leaves, conical, and rough-surfaced silica bodies adjacent to vascular bundle sclerenchyma; epidermal cells of pseudobulbs with heavily thickened outer walls, pseudobulb ground tissue of assimilatory and water-storage cells, scattered vascular bundles in pseudobulbs, and sclerenchyma and stegmata associated only with phloem of pseudobulbs; roots with thin-walled velamen cells and tenuous spirals of cell wall material, distinctive epivelamen cells, thin-walled exodermal cells and vascular tissue embedded in parenchyma. Except for mucilaginous idioblasts that occur in Mormodes and Cycnoches , there are few outstanding anatomical differences among the five genera. Thus, there are few anatomical characteristics of phylogenetic value. The monophyly of Catasetinae is supported by the presence of sunken foliar hairs. Our results support a close relationship between Clowesia and Catasetum , and between Mormodes and Cycnoches. Among the outgroups Pteroglossaspis is especially distinctive.     

Vegetative anatomy of subtribe Habenariinae (Orchidaceae)

Leaves of Habenariinae are characterized by anomocytic stomatal apparatuses, homogeneous mesophyll, collateral vascular bundles in a single series, and thin-walled bundle sheath cells. There is no foliar sclerenchyma nor a hypodermis. Cauline cortex consists of thin-walled living cells among which are large and numerous intercellular spaces. The ground tissue is bordered externally by a layer of thick-walled living cells, except in Habenaria repens. Central ground tissue cells are living, and usually thin-walled surrounding intercellular spaces of various dimensions. These are conspicuously large in H. repens. Collateral vascular bundles are scattered across the ground tissue. Sclerenchyma is absent. Absorbing roots are generally velamentous, exodermal dead cells are diin-walled, and passage cells usually have a thickened outer wall. A regular vascular cylinder is present, and vascular tissue is embedded in parenchyma. Root tubers are velamentous, exodermal cells are usually thin-walled, and passage cells frequently have thickened outer walls. Vascular tissue of root tubers is organized into two classes: (1) those with a single vascular cylinder surrounded by a cortex and (2) those with a series of meristeles dispersed throughout the ground tissue. In group (1) cortex is homogeneous either with or without mucilage cells except in Stenoglattis where the cortex is heterogeneous, consisting of water-storage and assimilatory cells, and lacks mucilage cells. In group (2) the ground tissue consists of larger mucilage-containing cells and smaller assimilatory cells.     

Comparative anatomy and systematics of Senghas's cushion species of Maxillaria (Orchidaceae)

Using data obtained through anatomy and morphology, we used cladistics to examine the monophyly of Senghas's proposed classification of Maxillaria cushion plants and his placement of Mormolyca ringens. Trignidium obtusum was chosen as the outgroup. Leaves have multicellular hairs sunken in crypts, primarily anomocytic or primarily tetracytic stomatal apparatuses, homogeneous mesophyll, and scattered fibre bundles. Three types of adaxial hypodermis were observed: (1) water-storage cells, (2) fibre bundles scattered among water-storage cells, and (3) fibre bundles scattered among chlorenchymatous cells. Abaxial hypodermis of fibre bundles occurs in several Maxillaria species and in Trigonidium obtusum. At the midvein of the leaf, adaxial mesophyll cells of most species are anticlinally extended and empty, and the abaxial mesophyll is usually collenchymatous. Vascular bundles are collateral and usually in a single series. Pseudobulb epidermal cell walls are thin, or outer walls are thickened. Ground tissue consists of water-storage and assimilatory cells with vascular bundles and associated lacunae scattered throughout. Roots are velamentous and exodermal cell walls are usually n-thickened with tenuous bands of scalarifom thickenings on longitudinal walls. Tilosomes may be plaited, baculate, or spongy. Endodermal cell walls are usually U-thickened and pericycle cell walls are usually O-thickened opposite phloem sectors. Stegmata line the periphery of the thickened pericycle cells opposite phloem sectors in M. picta. Pith may be parenchymatous or sclerenchymatous. According to our phylogenetic analysis, Mormolyca ringens is consistently nested within the cladistic structure of Maxillaria. Therefore, Maxillaria likely is paraphyletic if Mormolyca ringens is recognized as generically distinct. It appears that Senghas's subgroup divisions of the unifoliate pseudobulbous maxillarias may also be artificial.     

Comparative vegetative anatomy of Stanhopeinae (Orchidaceae)

Stanhopeinae are a group of tropical American orchids characterized by euglossine bee pollination and lateral inflorescences stemming from the bases of pseudobulbs. Leaves are hypostomatal, and all stomatal configurations are tetracytic. Chlorenchyma is homogeneous and characterized by fibre bundles in adaxial/abaxial or adaxial/median/abaxial positions. Collateral vascular bundles occur in a single row and feature phloic and xylic sclerenchymatous caps and thin-walled bundle sheath cells. Fibre bundles and vascular sclerenchyma are accompanied by stegmata containing conical silica bodies. Pseudobulbs have thick-walled turbinate epidermal cells and ground tissue of smaller, living assimilatory cells and larger, dead water-storage cells. Fibre bundles are usually absent but occur in several genera. Collateral vascular bundles show phloic sclerenchyma, but xylic sclerenchyma occurs only in die larger vascular bundles. Phloic and xylic sclerenchyma are associated with stegmata containing conical silica bodies. Roots are velamentous. Velamen cell walls have fine, spiral thickenings. Exodermal cells are thin-walled. The cortex features scattered thick-walled cells and in some cases branched bars of secondary cell wall material. Endodermis is either u-or O-thickened, but pericycle is always O-thickened opposite the phloem. Vascular tissue consists of alternating strands of xylem and phloem surrounded by a matrix of thick-walled cells. Pith cells may be parenchymatous or sclerenchymatous.     

菰适应湿地环境的解剖和屏障结构特征研究

菰(Zizania latifolia)是一种多年生挺水植物,为了探讨该植物根、茎和叶的解剖结构、组织化学及其质外体屏障的通透性生理。该文利用光学显微镜和荧光显微镜,对菰的根、茎、叶进行了解剖学和组织化学研究。结果表明:(1)菰不定根解剖结构由外而内分别为表皮、外皮层、单层细胞的厚壁机械组织层、皮层、内皮层和维管柱;茎结构由外而内分别为角质层、表皮、周缘厚壁机械组织层、皮层、具维管束的厚壁组织层和髓腔。叶鞘具有表皮和具维管束皮层,叶片具有表皮,叶肉和维管束。(2)不定根具有位于内侧的内皮层及其邻近栓质化细胞和外侧的外皮层组成的屏障结构;茎具内侧厚壁机械组织层,外侧的角质层和周缘厚壁机械组织层组成的屏障结构,屏障结构的细胞壁具凯氏带、木栓质和木质素沉积的组织化学特点,叶表面具有角质层。(3)菰通气组织包括根中通气组织,茎、叶皮层的通气组织和髓腔。(4)菰的屏障结构和解剖结构是其适应湿地环境的重要特征,但其茎周缘厚壁层和厚壁组织层较薄。由此推测,菰适应湿地环境,但在旱生环境中分布有一定的局限性。     

Leaf anatomical studies of Chamaecrista subsect. Baseophyllum (Leguminosae, Caesalpinioideae): new evidence for the up-ranking of the varieties to the species level

This study aims to determine whether morphoanatomical characters of the leaves of the species of Chamaecrista sect. Absus subsection Baseophyllum could be used to support an up-ranking of C. cytisoides varieties to the species level as previously defined by molecular studies. The significance of anatomical adaptive strategies to arid environments is also discussed. Standard light microscopy techniques and histochemical tests were used for both morphoanatomical and histochemical characterization of the leaves. All the species studied share a single-layered epidermis, actinodromous–camptodromous–brochidodromous type of venation, vascular bundles surrounded by layers of fibers bounded externally by a sheath of cells containing solitary crystals, enlarged tracheids at the vein endings, vascular petiole/rachis tissue with a parenchymatous pith, accessory vascular bundles, mucilage idioblasts and hypodermis in the mesophyll, colleters, and non-secretory trichomes. The position and type of stomata, type of mesophyll, number of palisade and spongy parenchyma layers, position of mucilage idioblasts in the mesophyll, and the number of accessory vascular bundles of petiole/rachis provided useful characters for discriminating the eight species of the subsect. Baseophyllum. Histochemical tests reveal the presence of total polysaccharides, pectins, mucilage and phenolic compounds in the idioblasts. Other xeromorphic characters such as thickened outer periclinal cell walls, compact mesophyll, mucilage idioblasts and hypodermis in the mesophyll may help enable the studied species to survive in exposed sunny areas.     

Vegetative anatomy of subtribe Orchidinae (Orchidaceae)

Leaves in Orchidinae are essentially glabrous; anticlinal walls of foliar epidermal cells arc basically straight-sided to curvilinear, and cells arc fundamentally polygonal on both surfaces; adaxial cells are larger than abaxial cells. Stomata arc anomocytic and usually only abaxial and superficial; substomatal chambers are small to moderate; outer and inner guard cell ledges are mostly small. There is no hypodermis nor are there fibre bundles. Mesophyll is homogeneous, chlorcnchyma cells arc thin-walled, and intercellular spaces numerous. Crystalliferous idioblasts abound. Vascular bundles are collateral, organized in a single series. and lack associated sclerenchyma. Bundle sheath cells are thin-walled and chlorophyllous. Stems are glabrous; stomata arc frequent in one species, lacking in others. Cortical cells are oval to circular, thick-walled, and interspersed with triangular intercellular spaces. Ground-tissue cells are circular, and triangular intercellular spaces are present. Vascular bundles arc collateral and scattered throughout the ground-tissue or are absent from the central ground-tissue. Epidermis in absorbing roots is one-layered and non-velamcntous. Exodcrmal cells are thin-walled and dead cell walls bear tenuous scalariform bars; some species lack an exodermis. Outer cortical cells are polygonal and lack intercellular spaces; middle layer cortical cells are rounded with triangular intercellular spaces; inner layer cells are polygonal and lack intercellular spaces. Endodermis and pericycle are thin-walled and one-layered. Vascular cylinder is mostly 7–9-arch with xylcm and phloem components alternating regularly; vascular tissue is embedded in parenchyma; pith cells are parenchymatous, polygonal, thin-walled and lack intercellular spaces. Root tubers generally bear a velamen of variable thickness; bulbous-based unicellular hairs frequently form a dense mat; exodermal cells are thin-walled; dead cells have scalariform bars, passage cells are sparse. Ground-tissue consists of rounded water-storage and assimilatory cells interspersed with triangular or quadrangular intercellular spaces; peripheral cells arc polygonal lacking intercellular spaces. Vascular tissue consists of monarch to pentarch meristeles distributed thoughout the ground-tissue each surrounded by a uniscriale endodermis of thin-walled cells. Thin roots ofPlalanthera exhibit a typical central cylinder surrounded by a homogeneous cortex uninterrupted by meristeles; thicker roots show a central vascular cylinder and cortex in which meristeles are also present; in globoid root tubers there is no central cylinder, and the ground-tissue is replete with scattered meristeles. Because the central vascular cylinder in Platanthera gives rise to branches (meristeles), these represent components of a single vascular system and are not separate stelar entities as implied by the use of the term ‘polystele’.     

Relictual vegetative anatomical characters in Cactaceae: the genusPereskia

The genusPereskia, which contains numerous morphological features considered relictual in the Cactaceae, has numerous anatomical features that we consider to be relictual also. These were studied to establish a basis for determining the ways that morphogenic mechanisms and anatomical characters diversified as the family evolved. ThesePereskia features may be relictual in the family: epidermis predominantly unistratose and lacking crystals; hypodermis absent or of about three layers of weakly collenchymatous cells with druses; cortex thin and predominantly parenchyma with druses and mucilage cells but lacking cortical bundles; secondary phloem without early differentiation of sclerenchyma but with secondary sclereids developing later, either idioblastically or in clusters; ergastic substances lacking from old secondary phloem; wood with a matrix of libriform fibers (mostly septate and nucleate), scanty paratracheal parenchyma, vessels solitary or in small clusters, perforations simple, pitting circular, oval or very broad; wide-band tracheids absent; ray cells slightly thick-walled, lignified, upright, isodiametric or procumbent; all primary rays narrow; pith without medullary bundles; leaves lacking hypodermis, with only weak development of palisade mesophyll; veins of four orders, strongly distinct in size, none with fibers; vessels in leaves narrower than those in stems.     

Leaf and twig anatomy of Eriope, a xeromorphic genus of Labiatae

The leaf and twig anatomy of 25 species of the genus Eriope were studied. The twig anatomy is very uniform apart from the level of formation of early layers of cork. Leaf anatomy shows considerable variation between the species, and this is correlated to some extent with the extreme habit range from trees to woody herbs. Characters of the lamina that show variation are: trichome type and frequency, cuticular markings, leaf dorsiventral or isobilateral, presence of adaxial stomata, presence of a hypodermis, number of layers of adaxial palisade mesophyll cells, occurrence of large bundles of phloem fibres at main veins, type of areolation and marginal venation. Petiole vasculature is simple and generally with either four distinct vascular bundles or two vascular arcs. The most xeromorphic species are usually woody herbs or sub-shrubs, and tend to have thick, isobilateral leaves with large bundles of phloem fibres and few hairs, or strongly dorsiventral leaves with a hypodermis and stomata in deep abaxial hair-lined depressions. The correlation of xeromorphic characters with environmental conditions is discussed. Leaf anatomy is of limited value in elucidating relationships within the genus.     

ANATOMICAL STUDIES OF CYATHEA AND TRICHIPTERIS (CYATHEACEAE)

Comparative anatomical studies of the mature stems of two species each of Trichipteris and Cyathea (Cyatheaceae) are described. The outermost boundary of the stem is typically a two-layered hypodermis. Mucilage-sac cells are randomly distributed in all parenchymatous areas of the stem and form articulated laticifer systems. Localized areas of sclerenchyma tissue occur in the cortex of both T. microphylla and C. suprastrigosa. All species studied possess medullary bundles, whereas cortical bundles are found only in T. trichiata. Accessory bundles occasionally are associated with indentations in the internal stelar sheath of T. trichiata. The stelar pattern in each genus is a dictyostele and consists of individual meristeles. Distinctive cubical cells typically occur wherever sclerenchymatous fibers and parenchyma cells abut one another. Tangential cells occur within the primary phloem of each meristele, and occasionally within the larger accessory bundles. The primary xylem of the adventitious roots is typically diarch, although triarch and tetrarch xylem may occur. Leaf traces and petiole strands are similar anatomically to the accessory bundles. Based upon this study Trichipteris and Cyathea show striking anatomical similarities, and appear to be closely-related taxa.     

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.     

Comparative vegetative anatomy and systematics of Cymbidium (Cymbidieae: Orchidaceae)

The genus Cymbidium (Orchidaceae) exhibits distinctive ecological diversification and occurs in terrestrial, epiphytic, and lithophytic life forms. One species, Cymbidium macrorhizon , lacks foliage leaves and has a strongly mycoparasitic existence. Correlation between habitat differentiation and anatomical characters was tested for 21 species of Cymbidium and its putative sister groups. Although hypostomaty characterizes the genus, C. canaliculatum shows amphistomaty. Ecological preference of this species indicates that amphistomaty is likely adapted to intensive insolation. Four types of subepidermal foliar sclerenchyma were found. Two forest floor species, C. goeringii and C. lancifolium as well as the mycoparasitic C. macrorhizon , do not have this sclerenchyma. In this genus, development of sclerenchyma is correlated with the degree of epiphytism. Palisade mesophyll evolved in Cymbidium section Cymbidium . As members of this section grow on isolated trees in tropical lowland forests or on rocks, the differentiation of palisade tissue is probably correlated with immigration to high light habitats. With the exception of C. macrorhizon , stegmata were found in leaves and stems of Cymbidium . Furthermore, a few epiphytic species have stegmata in their roots; this is a curious feature rarely found in vascular plants. Subterranean rhizomes characterize terrestrial species, while ageotropic roots are found in some epiphytic species. Cymbidium macrorhizon shows peculiar features such as degeneration of stomata, anomocytic stomata, and lack of stegmata and sclerenchyma. This set of character transformations is probably correlated with the evolution of mycoparasitic existence. © 2002 The Linnean Society of London, Botanical Journal of the Linnean Society , 2002, 138 , 383–419.     

Leaf and inflorescence peduncle anatomy: a contribution to the taxonomy of Rapateaceae

The anatomy of leaves and inflorescence peduncles was studied in species of Monotrema (4), Stegolepis (1) and Saxofridericia (1), aiming to contribute to the taxonomy of Rapateaceae. The form and structure of leaf blade midrib and the form of the inflorescence peduncle are diagnostic characteristics for the studied species. Monotrema is distinguished by: epidermal and vascular bundle outer sheath cells containing phenolic compounds in both organs; leaf blade with palisade and spongy chlorenchyma, arm-parenchyma, and air canals between the vascular bundles; leaf sheath with phenolic idioblasts in the mesophyll; inflorescence peduncle with tabular epidermal cells and air canals in the cortex and pith. Such characteristics support the recognition of Monotremoideae, which includes Monotrema. Stegolepis guianensis is distinguished by thick-walled epidermal cells and a plicate chlorenchyma in both organs; leaf blade with subepidermal fiber strands in abaxial surface and a heterogeneous mesophyll; inflorescence peduncle with rounded epidermal cells, a hypodermis with slightly thick-walled cells, and a pith with isodiametric cells and vascular bundles. Saxofridericia aculeata is distinguished by papillate epidermal cells in both organs; unifacial leaf blade with subepidermal fiber strands in both surfaces and a regular chlorenchyma; leaf sheath with a hypodermis in both surfaces and fiber bundles in the mesophyll; inflorescence peduncle with an undefined cortex and a hypodermis with thick-walled cells. S. guianensis shares few characteristics with S. aculeata, supporting their placement in different tribes.     

Epifluorescent and histochemical aspects of shoot anatomy of Typha latifolia L., Typha angustifolia L. and Typha glauca Godr

Using epifluorescent and histochemical techniques, we examined anatomical differences in the shoot organs of Typha latifolia, T. angustifolia and T. glauca. The leaf lamina of T. latifolia and T. glauca had enlarged epidermal cells and a thickened cuticle above the subepidermal vascular bundles; that of T. angustifolia lacked these characteristics. Leaf sheaths were similar among the species and all lacked the epidermal thickenings found in the lamina. The fertile stems had typical scattered vascular bundles with a band of fibres that was most prominent in T. glauca. The sterile stems were only 1 cm in length and contained a multiseriate hypodermis and a uniseriate endodermis over part of their length. The rhizomes were similar except for a pronounced band of fibres surrounding the central core in T. angustifolia. The rhizome was also characterized by an outer cortical region with a large multiseriate hypodermis/exodermis and a uniseriate endodermis with Casparian bands, suberin lamellae and secondarily thickened walls.     

Foliar sclereids in the Magnoliaceae

The foliar sclereids in 136 species representing 11 of the 12 genera of Magnoliaceae were studied and compared. Sclereids occur in four different cell assemblages within the leaf: diffuse idioblasts, mesophyll, dermal system, and the vein sheath including terminal elements. Tropical members tend to have the most highly sclerified leaves. In species of Manglietia the leaves have sclerified spongy mesophyll and either sclerified epidermis or hypodermis. In Talauma , sclerification affects the vein sheath and terminal cells of veinlets, with a specialized thick marginal vein in the Asian taxa but not in the American ones. Liriodendron and the magnolias native to the north temperate zone have only minimal sclerification, which usually is confined to the vein sheath of the midrib and the main lateral veins, and as idioblastic sclereids in the petiole and the midrib near the base of the blade. The two largest genera Magnolia and Michelia are heterogeneous and include species which vary as to their combinations of sclerified elements among the four possible types.     

Comparative anatomy and systematics of the orchid tribe Vanilleae excluding Vanilla

Vanilleae have been divided into three subtribes consisting of ten genera. We had material for study of all except Dictyophyllaria in subtribe Vanillinae. All genera except Vanilla have few species; Clematepistephium and Dictyophyllaria are monospecific. Leafy types have adaxial and abaxial stomata except Clematepistephium, Epistephium , and Eriaxis which have only abaxial tetracytic and anomocytic stomatal apparatuses. Cyrtosia, Erythwrchis, Galeola , and Lecanorchis are leafless. Hypodermis occurs in leaves of Pseudovanilla, Clematepistephium , and Eriaxis; leaves of Epistephium lack a hypodermis. Mesophyll is homogeneous. Stems of Cyrtosia, Galeola , and Eriaxis and rhizomes of Cyrtosia have a hypodermis. A uniseriate velamen occurs in roots of Erythrorchis, Pseudovanilla, Clematepistephium , and Lecanorchis; roots of other genera are bounded by a simple epidermis. Exodermal cell walls are n-thickened; endodermal cell walls are O-thickened. Vascular tissue of roots is variously embedded in sclerenchyma or parenchyma; similarly, pith may be sclerenchymatous or parenchymatous. Cladistic analyses result in two equally parsimonious trees with Epistephium and Eriaxis reversed in placement in each tree. Both trees constitute a paraphyletic complex giving rise to a clade containing the monophyletic Lecanorchidinae and Galeolinae. Vegetative anatomical characters have some phylogenetic value in Vanilleae, but they are not useful in resolving placement of the large and polymorphic genus Vanilla.     

沉香叶解剖结构的研究

通过石蜡切片法,光学显微镜观察,研究了沉香叶的解剖结构。结果表明,沉香叶为典型的异面叶,但具有许多旱生特征。表皮由一层排列紧密的形状不规则的表皮细胞组成,细胞外壁角质膜较厚,上表皮角质膜较下表皮的厚3.48μm,下表皮上零星分布着单细胞表皮毛,气孔类型为无规则型,仅分布在下表皮上,微下陷;叶肉组织发达,其间分布着较多的长方晶体,其长轴与表皮垂直;栅栏组织由1～2层圆柱形细胞组成,其外层细胞转化为异细胞,栅栏组织∶海面组织为1∶3.5,下表皮内具有1～2层由异细胞组成的下皮层;主脉发达,有异细胞组成的维管束鞘,具内生韧皮部;叶内具有发达的木质部外纤维。以上特征反映出植物结构与环境的统一性。     

贺兰山10种不同植物的旱生结构研究

对贺兰山10种不同生活型植物的形态解剖研究表明,长期生长在干旱贫瘠环境中植物,均形成适应生境的一些特殊形态结构．叶器官主要表现在：（1）叶表面积与体积之比缩小,表面覆有厚的角质膜,并被有表皮毛,气孔下陷,具孔下室;（2）栅栏薄壁组织细胞明显增多,海绵薄壁组织细胞减少．有叶肉不分化叶、等而叶和异而叶3种结构形式;（3）叶内贮水组织和机械组织增强。轴器官主要表现在：（1）根普遍形成周皮,且木栓层细胞层数增多;（2）机械组织非常发达,在周皮、皮层和韧皮部中有许多厚壁细胞分布。维管组织中的木薄壁细胞的细胞壁也明显木质化加厚;（3）有些植物的根具有异常维管组织。另外,这些植物根、茎、叶中均有粘液细胞和含晶细胞分布。这些结构具有重要的适应干旱生境的意义。     

蜈蚣草的解剖结构与组织化学特征

蜈蚣草（Pteris vittata）是多年生的超积累砷植物,并用于修复受重金属污染的土壤。利用光学显微镜和荧光显微镜来研究蜈蚣草的解剖结构及组织化学特征,以此明确该物种适应干旱岩生环境,以及具有离子超富集作用的特点。结果表明（：1）蜈蚣草孢子体的根状茎、不定根和叶的结构均为初生结构,不定根的结构由内而外包括维管柱、内皮层、皮层、木质化厚壁组织层和表皮。（2）根状茎结构由内而外包括网状中柱、内皮层、皮层、表皮外覆盖的角质层。（3）羽状复叶的总叶柄的结构由内而外包括维管束、内皮层、皮层、厚壁组织层、表皮外覆盖的角质层。叶片为异面叶,表皮内方具厚壁层,叶表皮具角质层,仅下表皮有气孔。（4）蜈蚣草根表皮、皮层与根毛的表面富含果胶,皮层木质化;黄连素离子通透性试验结果显示,根毛、根表皮和皮层滞留大量黄连素离子。综上,植物体的内皮层、木质化厚壁组织层、异面叶和厚的角质层结构说明蜈蚣草适应岩生环境,根具木质化皮层和富含果胶的组织化学特点,以及离子通透性试验表明其与离子超积累功能有关。     

Stem anatomy of Turbinicarpus s.l. (Cacteae,Cactaceae) and its contribution to systematics

The stem anatomy of Turbinicarpus s.l. was studied with the aims of finding characters to support the three clades (Rapicactus, Kadenicarpus, and Turbinicarpus) in which Turbinicarpus s.l. was recovered in the most recent phylogeny of the Cacteae tribe. Thirty-five taxa were prepared, and their tissues were compared. Substantial variation was found in the epidermal surface. The hypodermis has concentric druses (Rapicactus clade) or prismatic crystals (Kadenicarpus and Turbinicarpus clades) in the cell lumina. There are abundant collateral cortical bundles, but they are amphicribal in a few taxa, and xylary fibers occur in the Kadenicarpus clade. All members of Turbinicarpus s.l. have phloem without sclerenchyma and nonfibrous wood, except for T. subterraneus, which has wood with few fibers. The periderm has an epidermal origin, and the phellem may have thin-walled cells or alternating thin- to thick-walled layers. Our results support the three clades. The Kadenicarpus clade comprises the species with xylary fibers in cortical bundles, but it shares prismatic crystals in the hypodermis, thin-walled phellem cells and partially dilated rays with the Turbinicarpus clade. The members of the Rapicactus clade have concentric druses in the hypodermis. The anatomical features proved to be valuable to support the recognition of monophyletic clades.