Fused organs in the adherent1 mutation in maize show altered epidermal walls with no perturbations in tissue identities

In the absence of wounding, the epidermis is only rarely involved in cell or organ fusion events; in fact, intact epidermal layers prevent graft unions. In Zea mays L. the mutation adherent1 (ad1) shows abnormal fusions between cells and organs. Fusions involve epidermal cells of vegetative and floral organs and occur early in the ontogeny of organs. Even so, epidermal cell types differentiate normally in the fused regions and internal tissue identities are maintained. In contrast, the extracellular matrix (cell wall and cuticle) of the epidermal cells is perturbed. Epidermal cell walls in adherent leaves are thicker than normal. Epicuticular wax particles appear reduced in size and number and altered in shape in mutant leaves. In addition, the outer epidermal cell walls of adherent leaves fluoresce when stained with aniline blue, a reagent that binds to callose. Immunolocalizations to specific cell wall epitopes suggest that pectins but not arabinogalactans may have a role in the fusion events. Taken together, these results suggest that the ad1 mutation results in cell-wall and epicuticular-wax defects similar to responses seen in wounding, pollination by incompatible pollen, or pathogen attack. Since cell wall components and epicuticular waxes are extracellular secreted products, the ad1 mutation may disrupt normal functioning and/or composition of the secretory pathway and its cargo. Received: 30 January 1998 / Accepted: 5 March 1998     

EFFECTS OF 2,3,5-TRIIODOBENZOIC ACID ON THE STRUCTURE OF SOYBEAN LEAVES

The effects of 2,3,5-triiodobenzoic acid (TIBA) on soybean leaves (Glycine max. [L.] Merrill ‘Harosoy‘) include thickening with intensification of color and some raised intercostal regions, giving a wrinkled appearance. These effects are not restricted to early stages of leaf development but are pronounced during and after unfolding of the leaf. Proliferation of tracheary elements, increased procambial activity, and hypertrophy of bundle sheath extension cells occurred in the leaflet midvein of the youngest expanded leaf treated with 50 ppm or 100 ppm of TIBA. The youngest treated leaves exhibited differential growth rates and expansion within the palisade and spongy layers. Hypertrophy of spongy cells in these leaves occurred independently or simultaneously with elongation of the upper and lower palisade layers. The palisade and spongy tissues had undergone cell division and expansion at a greater pace than the epidermal layers. This, along with hypertrophy in the bundle sheath extension cells, would explain the wrinkled appearance of the lamina. The treated leaf became thicker than the control as a result of the increased number of cells in the spongy layer and elongation in the palisade layer. The observed aberrations in leaf structure suggest that TIBA interferes with some auxin-translocating system within the plant.     

Abnormal Stomatal Behaviour and Hormonal Imbalance in flacca, a Wilty Mutant of Tomato: EFFECT OF ABSCISIC ACID AND AUXIN ON STOMATAL BEHAVIOUR AND PEROXIDASE ACTIVITY

The wilty tomato mutant flacca and the normal variety RheinlandsRuhm were compared in terms of: (1) potassium transport intoand out of the guard cells, (2) cell wall properties which includeprotein, hydroxyproline and peroxidase activity, and (3) activityof indol-3yl-acetic acid oxidase. Also studied were the effectsof auxin on stomatal behaviour and peroxidase activity whenapplied to normal plants during development, and the short-termeffect of abscisic acid on the resistance of flacca stomatato closure under plasmolysis. Potassium transport, wall protein and hydroxyproline all seemedto be equal in mutant and normal plants. Peroxidase activitywas higher in the soluble and wall fractions of the mutant,and decreased toward normal in the mutant treated with abscisicacid. More stomata were open and peroxidase activity was higherin normal plants treated with auxin during development. Thepercentage of open stomata under plasmolysis was lower and theiraperture size was smaller in the epidermal strips taken fromabscisic-acid-treated mutant plants than from control mutantplants.     

SOME EFFECTS OF NITROGEN NUTRITION ON THE MORPHOLOGY AND ANATOMY OF MARROW-STEM KALE

Marrow-stem kale plants grown on plots receiving frequent additions of sulphate of ammonia showed a 40% increase in length of internode and a 25% increase in number of nodes per plant, and the leaf size was increased by between 50 and 70% over plants in plots receiving no N fertilizer. Leaves of kale continue to increase in area until they turn yellow, and the high N leaves showed a greater rate of increase in area at every stage in the life of the leaf.
Various features of leaf structure, such as stomatal index, and thickness of palisade and mesophyll, were unaffected by N treatment. The size of the epidermal cells of the leaves was very variable, and although the high N leaves showed a 12% increase in area per epidermal cell over the low N leaves, this difference is not statistically significant. The increased area of the high N leaves can therefore be attributed mainly to increased cell division during the life of the leaf. Only a very slight increase in rate of cell division is necessary to produce the observed effect.
The greater leaf area of the high N plants can be attributed mainly to increased size of individual leaves, but there was also a significantly greater number of living functional leaves per plant on the high N plants; at 23 weeks from sowing the high N plants had an average of 13.4 living leaves, while the low N plants had only 11.7 living leaves per plant.
There was an appreciable degree of N succulence in the high N kale leaves, which showed a 2% greater moisture content than the low N leaves.
A seasonal drift in epidermal cell size, palisade thickness, and total leaf thickness, is shown to be fully significant, statistically. Marked variations in stomatal frequency are barely significant at the 5% level.     

Compared Anatomy of Young Leaves of Prunus persica (L.) Batsch with Different Degrees of Susceptibility to Taphrina deformans (Berk.) Tul

Anatomical observations of leaves infected by Taphrina deformans were studied in tolerant peach trees (TPT) and in very susceptible (VSPT) ones. Leaves from the first sampling (2nd April) showed hyphae penetrating through the stomata or into the cuticle of the host tissue; anatomical structures of leaf sections were similar for both TPT and VSPT. The ultrastructure of the leaves of TPT showed seemingly normal mesophyll cells. In contrast, mesophyll cells of the VSPT showed important signs of degradation. Cells were organelle‐free and the middle lamella was expanded and invaded by hyphae of T. deformans. In some samples, the leaves of TPT showed deformed epidermal cells, loss of some spongy cells and increase of the intercellular spaces and division of the palisade cells. The pathogen proliferation in the leaves of the VSPT was considerably superior. In this case, stimulation of cell division occurred in the abaxial epidermis. Cells showed periclinal and oblique divisions, with an increased number of plasmodesmata; palisade or spongy cells were not differentiable. Leaves from TPT collected on 26th April showed hyphae with a non‐cylindrical section and with a squashed aspect. The hyphae were very evident in the intercellular spaces, showing abundant endoplasmic reticulum of rough type (RER) in the cytoplasm. On the other hand, epidermis of the leaves of the VSPT had numerous hyphae under the cuticle, which were growing in a thick pectin matrix. Leaves from TPT and VSPT collected on 6th May showed relevant differences. The leaves of TPT had a palisade mesophyll with fewer cells but with active chloroplasts. In contrast, the leaves from VSPT showed empty mesophyll cells, the cytoplasm was collapsed and the adaxial epidermis was covered with the fungus fructification. The observed anatomical and ultrastructural differences of leaves from TPT and VSPT confirm a different behaviour in plant‐host reaction at early stages of infection.     

THE DEVELOPMENT OF THE SEED OF ABUTILON THEOPHRASTI. II. SEED COAT

Winter , Dorothy M. (Iowa State U., Ames.) The development of the seed of Abutilon theophrasti. II. Seat coat. Amer. Jour. Bot. 47(3) : 157—162. Illus. 1960.–The integuments of Abutilon theophrasti Medic. undergo a rapid increase in size, predominantly by anticlinal cell divisions during the first 3 days after fertilization. Within 7 days, the outer epidermis of the inner integument becomes thick walled. At maturity this compact, lignified, and cutinized palisade layer accounts for more than half the thickness of the seed coat. During early growth, the palisade cells form a continuous layer in the micropylar region. In the chalazal region the palisade layer is discontinuous in a slit-shaped region, 60 × 740 microns. The shape of this discontinuity constitutes a major difference between dormant-seeded Abutilon and non-dormant Gossypium seeds. Exterior to the palisade layer is the outer integument which consists of a small-celled layer and a large-celled layer sparsely covered with unicellular, lignified hairs. Interior to the palisade is the thick mesophyll of the inner integument which is largely digested during seed growth and leaves only 2 pigmented cell layers in most regions at maturity. The inner epidermis is small-celled, pigmented and cutinized and adheres tightly to the endosperm. Seed coat impermeability increases with seed maturity. Even immature seeds will germinate, if scarified, indicating a lack of embryo dormancy.     

ISOLATION AND CHARACTERIZATION OF A CELL WALL‐DEFECTIVE MUTANT OF CHLAMYDOMONAS MONOICA (CHLOROPHYTA)1

Cell wall–defective strains of Chlamydomonas have played an important role in the development of transformation protocols for introducing exogenous DNA (foreign genes or cloned Chlamydomonas genes) into C. reinhardtii. To promote the development of similar protocols for transformation of the distantly related homothallic species, C. monoica, we used UV mutagenesis to obtain a mutant strain with a defective cell wall. The mutant, cw‐1, was first identified on the basis of irregular colony shape and was subsequently shown to have reduced plating efficiency and increased sensitivity to lysis by a non‐ionic detergent as compared with wild‐type cells. Tetrad analysis of crosses involving the cw‐1 mutant confirmed 2:2 segregation of the cw:cw⁺ phenotypes, indicating that the wall defect resulted from mutation of a single nuclear gene. The phenotype showed incomplete penetrance and variable expressivity. Although some cells had apparently normal cell walls as viewed by TEM, many cells of the cw‐1 strain had broken cell walls and others were protoplasts completely devoid of a cell wall. Several cw‐1 isolates obtained from crosses involving the original mutant strain showed a marked enhancement of the mutant phenotype and may prove especially useful for future work involving somatic cell fusions or development of transformation protocols.     

STRUCTURE OF THE LEAF OF PYROSSIA LONGIFOLIA—A FERN EXHIBITING CRASSULACEAN ACID METABOLISM

The leaf of Pyrossia longifolia (Burm.) Morton, an epiphytic fern known to exhibit CAM, was examined by light and electron microscopy. The relatively thick leaf contains a single-layered epidermis, “water-storage” tissue, and a reticulate vascular system embedded in mesophyll tissue not differentiated into palisade and spongy layers. Mesophyll is composed of large, slightly elongate cells each with a thin, parietal layer of cytoplasm and a large central vacuole. The chloroplast-microbody ratio in mesophyll cells indicates that Pyrossia may be a high photorespirer and thus similar in that sense to C₃ plants. Mesophyll is separated from the vascular tissue by a tightly-arranged layer of endodermal cells with Casparian strips. The inner layer of mesophyll cells and the endodermal cells lack suberin lamellae. The collateral veins contain sieve elements, tracheary elements, pericycle and vascular parenchyma cells, the latter conspicuously larger than the sieve elements. The vascular parenchyma is the only cell type in the leaf which contains plastids with a peripheral reticulum. The parenchymatic elements of the leaf are connected by plasmodesmata, all of which lack neck constrictions and sphincters, or sphincter-like structures. The connections between sieve elements and adjacent parenchymatic elements are pore-plasmodesmata characterized by prominent wall thickenings on the parenchymatic-element side of the wall. The distribution and relative frequencies of plasmodesmata between the various cell types of the leaf indicate photoassimilates may move either symplastically or by a combination of symplast and apoplast from the mesophyll to the site of phloem loading in the veins.     

Leaf anatomy of <Emphasis Type="Italic">Cynara scolymus</Emphasis> L. in successive micropropagation stages

Summary Leaf structure along the successive stages of Early French artichoke Cynara scolymus L. micropropagation was characterized using light and transmission electron microscopy. The mesophyll presents disorganized spongy and palisade parenchyma with large intercellular spaces and a few small chloroplasts in the leaves of plants cultured in vitro. In addition, both epidermal surfaces of such leaves invariably show a cell wall of the same thickness with a very thin cuticle and open stomata. In the root differentiation stage in vitro, structural changes take place in the leaves that are favorable for survival in the acclimatization stage: conspicuous cuticle, greater cell wall thickness, functional stomata, better mesophyll organization, developed vascular bundles, and the presence of sclerenchymatous tissue are observed. These features found in later in vitro stages are maintained in the following ex vitro stages, some becoming more evident. Our results demonstrate that the structural changes required to ensure appropriate acclimatization of micropropagated artichoke plants begin at the root differentiation stage, which can reduce in vivo acclimatization time and achieve greater survival of transferred plants.     

Palisade mesophyll cell expansion during leaf development in Zinnia elegans (Asteraceae)

Temporal and spatial patterns of palisade mesophyll cell expansion in Zinnia elegans were characterized as a basis for developing a suspension culture model for mesophyll cell expansion. Our objectives were to 1) identify the leaf regions from which cells in various stages of expansion could be selectively isolated for culture, and 2) develop a basis for comparison of rate and extent of mesophyll cell expansion in culture with that in the leaf. Palisade mesophyll cells were isolated from expanding leaves by gentle physical maceration without the use of enzymes. Isolated cells from leaves in different stages of expansion were then measured by computer image analysis. Analysis of size frequency distributions showed that unexpanded cells can be isolated from the entire blade of small leaves or the basal regions of partially expanded leaves. Fully expanded cells can be obtained from the apical and middle regions of partially expanded leaves. Within the leaf, Zinnia mesophyll cells expanded from about 400 μm² to about 2.300 μm² at an estimated rate of 160 μm² d^-1. The percent increase in cell length exceeded the percent increase in cell width. Expansion of mesophyll cells continued for 6–8 d after epidermal expansion ceased. This difference in the timing of cell expansion in epidermal and mesophyll cells indicates that different regulatory factors may be operating in these adjacent tissues and underscores the importance of investigating the regulation of mesophyll cell expansion at the cellular level.     

A novel feature of structural variegation in leaves of the tropical plant Schismatoglottis calyptrata

We report a novel feature of leaf variegation. As is often the case in tropical forest floor herbs, Schismatoglottis calyptrata leaves feature structural variegation. Examination of leaf anatomy in S. calyptrata revealed a novel feature of structural variegation, which was generated by variation in the spatial arrangement of the adaxial-most tip of the palisade cells. In fully green leaf parts, contact between the adaxial-most tip of the palisade cells and the cone-shaped base of the outer epidermis cells was tight, and palisade cells were arranged radially around each epidermal cell. In dull, grayish-green leaf parts, the contact was loose, and no particular spatial arrangement of palisade cells relative to epidermal cells was observed. This feature of structural variation could be disadvantageous for photosynthesis efficiency in view of the hypothesis that, for rainforest herbs, cone-shaped epidermal cells may function as lenses. However, the high frequency of leaf variegation of S. calyptrata in natural habits suggests that this structural variegation plays an unknown advantageous role.     

LEAF DEVELOPMENT IN THE NORMAL AND SOLANIFOLIA MUTANT OF TOMATO (LYCOPERSICON ESCULENTUM)

Leaf development in the normal (lobed margin) and the solanifolia (sf/sf) mutant (entire margin) of tomato (Lycopersicon esculentum) was compared at the light and scanning electron microscope levels. The shoot apices of the mutant plants contained microbodies near the axil of the youngest leaf, which were absent in the normal plants. The structural and morphological events in the initiation of leaf primordia were similar in the two genotypes. The pattern of leaflet emergence was also similar in the two types of plants, but the timing of leaflet production was different. The first pair of leaflet primordia in the normal plants was produced on P₃, whereas in the mutant it was not produced until P₅. The adult leaves of sf/sf plants were larger than those of normal, and the greater leaf area in the mutant was associated with a greater adaxial epidermal cell and areole area. A continuous marginal fimbriate vein (MFV) was present along the margin of each of the normal leaflets. However, a continuous MFV was absent in the mutant leaflets. It is suggested that the absence of a continuous MFV in the mutant might alter the nutritional and hormonal supply to the leaf margin, which ultimately leads to a modified leaf, i.e., with an entire margin.     

不同色彩珙桐叶片和苞片解剖结构及色素含量比较研究

以生长于同一生境下的粉红珙桐(粉红色叶片、苞片)与普通珙桐(绿色叶片、白色苞片)为试材,对比两种色彩珙桐叶片/苞片解剖结构和色素含量的差异,以揭示珙桐色彩转变的规律。结果显示：(1)两种珙桐叶片均属于异面叶类型,栅栏组织由一层长柱形细胞整齐排列而成,海绵组织排列疏松,部分粉红叶片的上表皮细胞向外凸起,绿叶无此现象;粉红叶片的总厚度及其表皮角质层、栅栏组织和海绵组织厚度都高于绿叶,而表皮较薄。(2)两种珙桐苞片均无栅栏组织和海绵组织的分化,粉红苞片上表皮细胞明显隆起,上表皮角质层增厚,而下表皮变薄。(3)粉红叶片的类黄酮、花色苷含量分别是绿色叶片的1.52倍、3.67倍,两者的光合色素含量无显著差异,但粉红叶片的叶绿素a/b值比绿色叶低很多;粉红苞片花色苷含量显著高于白色苞片,而两者类黄酮含量差异不大。研究表明,花色苷是珙桐叶片和苞片色彩转红的直接因素,类黄酮有助于叶片呈红色;粉红珙桐叶片/苞片的解剖结构发生了一定变化,对光能的利用效率更高,对阴湿环境的适应性增强。     

THE ULTRASTRUCTURE OF THE SALT GLANDS OF CYNODON AND DISTICHLIS (POACEAE)

The epidermal salt glands of the grasses Cynodon and Distichlis consist of a small outer cap cell and a large, flask-shaped basal cell. The wall of the basal cell is contiguous with those of the adjacent epidermal cells and underlying mesophyll cells. The basal cell is connected symplastically with all adjoining cells via plasmodesmata. The outer, protruding portion of the glands is covered by a cuticle continuous with that of the adjoining epidermal cells. However, the lateral cell walls of the glands are not incrusted by this cuticle. The cap cell wall has a loose, mottled appearance quite different from the compact striated appearance of the basal cell wall. The cap cell is characterized by dense cytoplasm containing many organelles and a varying number of small vacuoles. The basal cell cytoplasm is distinguished by the presence of an intricate system of paired membranes that are closely associated with mitochondria and microtubules. These membranes are infoldings of the plasmalemma that originate adjacent to the wall separating the cap and basal cells. The space enclosed by the paired membranes, therefore, is an extracellular channel that is open only in the direction of secretory flow. The consistent orientation of this system of paired membranes suggests that it represents a structural specialization which is directly and functionally involved in the secretory process. The close association of mitochondria and microtubules with the paired membranes implies that these structures are also functionally related to the secretory process. Finally, the results of this study indicate that these glands are ultrastructurally similar to those of Spartina and that the glands of these three grasses are structurally distinct from those of dicotyledonous plants.     

LEAF ANATOMY OF TISSUE-CULTURED LIQUIDAMBAR STYRACIFLUA (HAMAMELIDACEAE) DURING ACCLIMATIZATION

Structural changes accompanying the acclimation process were observed in leaves of sweetgum, Liquidambar styraciflua, using light and transmission electron microscopy (TEM). Comparisons were made of leaves obtained from tissue culture, plantlets acclimated after transfer from the in vitro environment to soil, and field grown trees. Leaves of cultured plantlets lacked a differentiated palisade parenchyma and had spongy parenchyma interspersed with large air spaces. Field grown leaves showed distinct palisade and spongy tissues and a high cell density. New leaves from acclimated plantlets showed an elongation of the upper mesophyll with fewer intercellular spaces than cultured plants. Cells from leaves from in vitro plantlets had large vacuoles, limited cytoplasmic content and flattened chloroplast with an irregularly arranged internal membrane system. Acclimated and field leaf cells had a greater cytoplasmic content than cultured leaves, with the former having more dominate vacuoles. Chloroplasts had evident grana. Acclimated and field leaves had a well developed cuticle unlike leaves from culture.     

Anatomy, palynology and nutlet micromorphology of Turkish endemic Teucrium sandrasicum (Lamiaceae)

In this study, the anatomical features of the leaf and stem, besides the pollen and nutlet characteristics of Teucrium sandrasicum are investigated. T. sandrasicum, belonging to sect. Teucrium, is an endemic perennial herb growing on serpentine around Muğla province. The anatomical studies on T. sandrasicum revealed that the stem shares the general characteristics of the Labiatae family. The leaves clearly exhibit xeromorphy due to features such as the distribution of stomata on the lower surface (hipostomatic), the occurrence of guard cells below the epidermis (xeromorphic type), inrolled margins, thick cuticle layer, thick outer epidermal cell wall, a high density of trichomes and thick palisade layer of the mesophyll. The anatomical studies showed that the upper epidermal cells of the leaf include many spherocrystals. The pollen grains are prolate, medium in size, 3-colpate with verrucate ornamentation. The nutlets are ellipsoid with a reticulate-verrucate surface. The results have proven that T. sandrasicum is different from the other species of the sect. Teucrium because of the branched trichomes on the stem and the lack of eglandular trichomes on the nutlets.     

DEVELOPMENT OF THE CUTICULAR LAYERS IN ANGIOSPERM LEAVES

Schieferstein , R. H., and W. E. Loomis . (Iowa State U., Ames.) Development of the cuticular layer in angiosperm leaves. Amer. Jour. Bot. 46(9): 625–635. Illus. 1959.—The cuticularized layers of leaves and other plant surfaces consist of a primary cuticle, formed by the oxidation of oils on exposed cell walls, plus various surface and subsurface wax deposits. The primary cuticle appears to form rapidly on the walls of any living cell which is exposed to air. Surface wax is present on the mature leaves of about half of the 50 or 60 species studied. In general, wax is extruded at random through the newly formed cuticle of young leaves and accumulated in various reticulate to semicrystalline patterns. No wax pores through the cuticle or primary wall can be observed in electron-micrographs of dewaxed mature leaves. Wax accumulations on older leaves are generally subcuticular and may involve the entire epidermal wall. These deposits appear to be of considerably greater ecological significance than those on the surface. Isolated cuticular membranes from Hedera helix increased slightly in permeability to water with age of the leaf, but permeability to 2,4-D decreased 50 times. Evidence based on the patterns of cellulose in primary walls, of surface wax on growing leaves, of the appearance of the cuticle at the margins of growing epidermal cells, of the forms of the cuticle plates digested from growing and older leaves, and of the marginal location of new wax deposits on growing maize leaves is presented to support the thesis that the enlargement of the outer surface of the epidermal cells of leaves occurs at the margins of the surface. Earlier formed cuticle and wax are thus undisturbed during growth. These observations, coupled with evidence for apical growth in fibers, root hairs, etc. suggest that the primary walls of angiosperm cells are formed in specific, localized growth regions, rather than by plastic extension and apposition.     

枫香变红过程中叶片组织结构、光合特性及色素含量变化研究

枫香(Liquidambar formosana)因其叶片入秋后逐渐变红而极具观赏价值,是优良的景观生态树种。为了解枫香叶片结构变化与叶色的关系,该文通过连续监测枫香叶片变红过程中组织结构、光合特性及色素含量的变化,分析叶片结构与其光合特性和色素的关系。结果表明：(1)叶片变色过程中,表皮细胞均为椭圆形,紧密排列,未观察到明显的细胞变异,表面未附着绒毛和蜡质,且上表皮细胞与栅栏组织细胞间排列紧密,未出现较大的气室。(2)随着叶片逐渐变红,叶片结构变化显著,其中叶片、上表皮、栅栏组织和海绵组织厚度及气孔开度均逐渐减小,而气孔器长和宽、单个气孔器面积则逐渐增大。(3)随着叶片结构的变化,其叶绿素含量逐渐减少,致使净光合速率逐渐减小,在出现光破坏时,叶片通过在栅栏组织细胞液泡内合成花色苷来自我保护,而大量的花色苷致使叶片表面呈现红色。综上认为,叶绿素含量降低,花色素苷大量积累是导致枫香叶片变红的直接原因,而枫香叶色变红则是其一系列生理结构特征综合作用的结果。     

THE DEVELOPMENT OF APOSPOROUS GAMETOPHYTES AND REGENERATED SPOROPHYTES FROM EPIDERMAL CELLS OF EXCISED FERN LEAVES: AN ANATOMICAL STUDY

Three different types of outgrowths develop from epidermal cells of excised juvenile leaves of Microgramma vacciniifolia: aposporous gametophytes, intermediates, and regenerated sporophytic plantlets. The gametophytes and intermediates arise from derivatives of epidermal cell divisions which are developed to the exterior of the leaf surface, whereas the sporophytic regenerants originate from derivatives produced by cell divisions to the interior of the leaf. Anatomical observations of excised leaves grown in vitro demonstrate that only the epidermal cells are stimulated to divide and give rise to the various types of outgrowths. Incorporation of tritiated thymidine by the nuclei of leaf epidermal cells gives further evidence for the metabolic activity of these cells.