Structure of a stem-derived callus of Ruta graveolens: meristems, leaves, and secretory structures

1978 ◽  
Vol 56 (21) ◽  
pp. 2717-2729 ◽  
Author(s):  
R. L. Peterson ◽  
M. G. Scott ◽  
B. E. Ellis
Keyword(s):  
Endoplasmic Reticulum ◽  
Cell Walls ◽  
Light And Electron Microscopy ◽  
Middle Lamella ◽  
Subsequent Development ◽  
Callus Cultures ◽  
Ruta Graveolens ◽  
Secretory Structures ◽  
Apical Meristems ◽  
Secretory Glands

Differentiation in a stem-derived callus of Ruta graveolens was studied by correlated light and electron microscopy. Shoot apical meristems, some of which initiated leaves, differentiated randomly at the surface of the callus. Some of the apical meristems had a tunica–corpus organization. Cells of the tunica and corpus had large nuclei with prominent nucleoli, small vacuoles, mitochondria, endoplasmic reticulum cisternae, and leucoplasts. The leaves were radial and had well developed stomata and chloroplasts of two types, one storing large starch grains and the other with no starch but with well developed grana. Lysigenous and schizolysigenous secretory glands were initiated in the leaves and towards the periphery of the callus. Central cells in the lysigenous glands underwent lysis forming a gland lumen into which lipid-like material from the degenerating cells was released. During early stages of cell lysis, breakdown of the middle lamella occurred, followed by the degeneration of cell walls. The lipid-like deposits are thought to be the essential oils known to be produced by these callus cultures. Schizolysigenous glands are formed by the separation of gland cells along the middle lamella and the subsequent development of an epithelial layer or layers surrounding a gland lumen. The cytology of epithelial cells was characterized by numerous ribosomes and the presence of plastids with lipid-like deposits, rough endoplasmic reticulum which occurred either as sheets of cisternae or tubular profiles, and osmiophilic deposits in the cytoplasm. Changes in the epithelial cell walls bordering on the gland lumen indicated that these cells were probably undergoing lysis in older stages of gland development.

scholarly journals Abscission Layer Formation as a Resistance Response of Peruvian Apple Cactus Against Glomerella cingulata

2002 ◽  
Vol 92 (9) ◽  
pp. 964-969 ◽  
Author(s):  
Young Ho Kim ◽  
Kwang-Hyung Kim
Keyword(s):  
Cell Wall ◽  
Cell Division ◽  
Cell Walls ◽  
Light And Electron Microscopy ◽  
Middle Lamella ◽  
Fungal Culture ◽  
Glomerella Cingulata ◽  
Abscission Layer ◽  
Resistance Response ◽  
Initial Cell

Stem disks from 2-year-old cacti Cereus tetragonus (susceptible) and C. peruvianus (resistant) were inoculated in the center (pith) with Glomerella cingulata isolated from Colletotrichum stem rot in three-angled cacti. The susceptible cactus became extensively colonized, whereas colonization was limited to a small area in the resistant cactus. The resistant cactus formed prominent abscission layers (ALs) in parenchyma internal to the inoculation site. Ethanol extracts of the fungal culture also stimulated AL formation in the resistant cactus. Initial cell division followed at 2 to 4 days after treatment, and layering of multiple cells at 7 days after treatment. After 10 days, the outer layers were sometimes sloughed from the inner layers. No AL formation was induced in susceptible C. tetragonus treated with ethanol extract or in untreated control cacti. Light and electron microscopy revealed that initial cell division occurred by cell wall formation, and that an additional cell wall was layered in pre-existing parenchyma cells without ordinary cell division. Later, separation layers formed in ALs where inner cell walls appeared to be thickened secondarily, and the cell walls and middle lamella within the layer dissolved. These results suggest that AL formation in the resistant cactus is induced by fungal metabolites, and that it serves as a histological barrier against anthracnose pathogens.

Histology and ultrastructure of caulogenic callus cultures of Larix ×eurolepis

1990 ◽  
Vol 68 (5) ◽  
pp. 979-989 ◽  
Author(s):  
Sylvie Laliberté ◽  
Maurice Lalonde
Keyword(s):  
Cell Walls ◽  
Callus Tissue ◽  
Light And Electron Microscopy ◽  
Adventitious Shoots ◽  
Callus Cultures ◽  
Starch Granules ◽  
Hybrid Larch ◽  
Short Shoot ◽  
Green Areas ◽  
Extracellular Substances

Caulogenic callus cultures intiated from vegetative short shoot buds of a mature Larix ×eurolepis Henry (hybrid larch) were studied by light and electron microscopy. Callus tissue showed a zonation in pigmentation, as color varied from green to tan and brown. Green areas displayed characteristics of actively growing tissues, contained numerous chloroplasts and starch granules, and showed a range in the amount of vacuolar tannin deposits. Vascular clusters were present in callus tissue associated with adventitious shoots, which were well vascularized. Tan and brown areas had massive amounts of starch granules, tannin deposits, and sclereids. Numerous cells in brown areas were in a senescent state. Browning of tissues increased with time during each subculture and was concomitant with an increase in shoot productivity. Extracellular substances were apparently extruded from primary cell walls in tan and brown areas. Key words: caulogenic calli, conifer, histology, Larix, tissue culture, ultrastructure.

scholarly journals The secretory glands of Asphodelus aestivus flower

Biologia ◽  
2008 ◽  
Vol 63 (6) ◽  
Author(s):  
Thomas Sawidis ◽  
Elzbieta Weryszko-Chmielewska ◽  
Vasiliki Anastasiou ◽  
Artemios Bosabalidis
Keyword(s):  
Endoplasmic Reticulum ◽  
Nectar Secretion ◽  
Secretory Structures ◽  
Golgi Bodies ◽  
Floral Nectary ◽  
Septal Nectary ◽  
Mediterranean Type Ecosystem ◽  
Secretory Glands ◽  
Mucilage Gland ◽  
Asphodelus Aestivus

AbstractVarious secretory glands are observed on Asphodelus aestivus flower, a common geophyte of Mediterranean type ecosystem. The floral nectary has the form of individual slits between the gynecium carpels (septal nectary). The septal slits extend downwards to the ascidiate zone of the carpels. The nectar is secreted by the epidermal cells of the slits, which differentiate into epithelial cells. The latter contain numerous organelles, among which endoplasmic reticulum elements and golgi bodies predominate. Nectar secretion results in an expansion of the space between the septa. The nectar becomes discharged through small holes on the ovary wall. Six closely packed stamens surround the ovary and bear numerous papillae at their basis. These papillae are actually osmophores, i.e. secretory structures responsible for the manufacture, secretion and dispersion of terpenic scent. A mucilage gland (obturator) exists between the lateral ovule and the ovary septa, giving a positive reaction with Schiff’s reagent. This gland secretes a mucoproteinaceous product to nourish the pollen tube and to facilitate its penetration into the ovary.

scholarly journals The Fine Structure of the Wheat Scutellum Before Germination

1972 ◽  
Vol 25 (1) ◽  
pp. 9 ◽  
Author(s):  
JG Swift ◽  
TP O'brien
Keyword(s):  
Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Fine Structure ◽  
Coat Protein ◽  
Storage Protein ◽  
Cell Walls ◽  
Lipid Droplets ◽  
Light And Electron Microscopy ◽  
Ground Substance ◽  
Nuclear Chromatin

The structure of the cells of the scutellar epithelium and parenchyma is described and illustrated by light and electron microscopy of air-dry grains and compared with that seen in grains soaked for 3 hr. In the air-dry state, nuclear chromatin is strongly aggregated, mitochondria and plastids appear to be intact, endoplasmic reticulum is present but not abundant, and dictyosomes cannot be readily identified. The ground substance contains an abundance of free ribosomes which appear to coat protein bodies, lipid droplets, and mitochondria. In material soaked only for 3 hr, endoplasmic reticulum and dictyosomes are apparent, the nuclear chromatin has dispersed, and some mobilization of storage protein appears to have begun in the scutellar epithelium. No differences in fine structure of other organelles or in the cell walls could be detected.

Silicification of wood-cell walls

1994 ◽  
Vol 52 ◽  
pp. 428-429
Author(s):  
S. E. Keckler ◽  
D. M. Dabbs ◽  
N. Yao ◽  
I. A. Aksay
Keyword(s):  
Electron Microscopy ◽  
Cell Wall ◽  
Cell Walls ◽  
Lignin Content ◽  
Resin Composite ◽  
Middle Lamella ◽  
Cellulose Fibers ◽  
Complex Structures ◽  
Rich Region ◽  
Inorganic Precursors

Cellular organic structures such as wood can be used as scaffolds for the synthesis of complex structures of organic/ceramic nanocomposites. The wood cell is a fiber-reinforced resin composite of cellulose fibers in a lignin matrix. A single cell wall, containing several layers of different fiber orientations and lignin content, is separated from its neighboring wall by the middle lamella, a lignin-rich region. In order to achieve total mineralization, deposition on and in the cell wall must be achieved. Geological fossilization of wood occurs as permineralization (filling the void spaces with mineral) and petrifaction (mineralizing the cell wall as the organic component decays) through infiltration of wood with inorganics after growth. Conversely, living plants can incorporate inorganics into their cells and in some cases into the cell walls during growth. In a recent study, we mimicked geological fossilization by infiltrating inorganic precursors into wood cells in order to enhance the properties of wood. In the current work, we use electron microscopy to examine the structure of silica formed in the cell walls after infiltration of tetraethoxysilane (TEOS).

UV-microscopic analysis of acetylated spruce and birch cell walls

Holzforschung ◽  
2004 ◽  
Vol 58 (5) ◽  
pp. 483-488 ◽  
Author(s):  
Christian Hansmann ◽  
Manfred Schwanninger ◽  
Barbara Stefke ◽  
Barbara Hinterstoisser ◽  
Wolfgang Gindl
Keyword(s):  
Cell Walls ◽  
Middle Lamella ◽  
Microscopic Analysis ◽  
Weight Percent ◽  
Cellular Level ◽  
Uv Spectrum ◽  
Spectral Shifts ◽  
Microscopy Analysis ◽  
Absorbance Peak ◽  
Absorbance Spectra

Abstract Spruce and birch earlywood was acetylated to different weight percent gains using three different acetylation procedures. The absorbance spectra of secondary cell wall and compound cell corner middle lamella were determined by means of UV microscopy. Analysis of the spectra showed that the characteristic lignin absorbance peak in the UV spectrum of wood around 280 nm shifted to shorter wavelengths in acetylated samples. A distinct relationship between achieved weight percent gains after acetylation and observed spectral shifts could be established revealing a certain potential to measure acetylation on a cellular level by means of UV microscopy.

scholarly journals STUDIES ON MICROPEROXISOMES II. A CYTOCHEMICAL METHOD FOR LIGHT AND ELECTRON MICROSCOPY

1972 ◽  
Vol 20 (12) ◽  
pp. 1006-1023 ◽  
Author(s):  
ALEX B. NOVIKOFF ◽  
PHYLLIS M. NOVIKOFF ◽  
CLEVELAND DAVIS ◽  
NELSON QUINTANA
Keyword(s):  
Endoplasmic Reticulum ◽  
Guinea Pig ◽  
Lipid Droplets ◽  
Smooth Endoplasmic Reticulum ◽  
Light And Electron Microscopy ◽  
Distal Tubule ◽  
Striking Difference ◽  
High Concentration ◽  
Electron Microscopic ◽  
Pig Kidney

A modification of the Novikoff-Goldfischer alkaline 3,3'-diaminobenzidine medium for visualizing peroxisomes is described. It makes possible light microscopic as well as electron microscopic studies of a recently described class of peroxisomes, the microperoxisomes. Potassium cyanide (5 x 10–3 M) is included in the medium to inhibit mitochondrial staining, the pH is 9.7 and there is a high concentration of H2O2 (0.05%). Two cell types have been chosen to illustrate the advantages of the new procedure for demonstrating the microperoxisomes: the absorptive cells in the human jejunum and the distal tubule cells in the guinea pig kidney. Suggestive relations of microperoxisomes and lipid are described in the human jejunum. The microperoxisomes are strategically located between smooth endoplasmic reticulum that radiates toward the organelles and contains lipid droplets and "central domains" of highly specialized endoplasmic reticulum which do not show the lipid droplets. The microperoxisomes are also present at the periphery of large lipid-like drops. In the guinea pig kidney tubule there is a striking difference between the thick limb of Henle and distal tubule. The distal tubule has a population of cells with large numbers of microperoxisomes readily visible by light microscopy; these cells are not present in the thick limb of Henle. Other differences between the two are also described.

scholarly journals The Lamellar Systems of Cytoplasmic Membranes in Dividing Spermatogenic Cells of Drosophila virilis

1960 ◽  
Vol 7 (3) ◽  
pp. 433-441 ◽  
Author(s):  
Susumu Ito
Keyword(s):  
Endoplasmic Reticulum ◽  
Golgi Complex ◽  
Light And Electron Microscopy ◽  
Primary Spermatocyte ◽  
Drosophila Virilis ◽  
Spermatogenic Cells ◽  
Membrane Systems ◽  
Cytoplasmic Membranes ◽  
Pas Reaction ◽  
Staining Methods

Spermatogenic cells of Drosophila virilis were studied by light and electron microscopy. The persistence of a "nuclear wall" during the meiotic divisions has been reported by a number of early cytologists, but this interpretation has been a subject of debate. Electron micrographs of dividing spermatocytes reveal the presence of multiple layers of paired membranes surrounding the nuclear region. These lamellar membrane systems are not typical of the nuclear envelope, but were interpreted as such by light microscopists. The membranes constituting a pair are separated by an interspace of ∼ 100 A and successive pairs are 200 to 400 A apart. These spacings are similar but not identical to those found in the lamellar systems of the Golgi complex. The cisternae of the endoplasmic reticulum in this material are devoid of attached ribonucleoprotein particles, are more precisely ordered than in vertebrate cells, and show a uniform, narrow intracisternal space of ∼ 100 A. The conspicuous asters appear to be made up of similar paired membranes radiating from the centriolar region. The primary spermatocyte has numerous dictyosomes and a well developed endoplasmic reticulum in cisternal form, but no typical Golgi complex or endoplasmic reticulum is found during the meiotic division stages of metaphase to telophase. Evidence is presented that these cytoplasmic organelles contribute to the formation of the extensive lamellar systems that appear during meiosis. The results of the Golgi silver staining methods and staining tests for phospholipids, basophilia, and the PAS reaction, indicate that the lamellar arrays of membranes present during meiosis are indistinguishable from the Golgi complex in their tinctorial properties.

Phase-contrast and electron-microscopic observations on a membranous complex in primary spermatocytes of the mouse

1975 ◽  
Vol 18 (1) ◽  
pp. 1-17
Author(s):  
A. Pleshkewych ◽  
L. Levine
Keyword(s):  
Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Phase Contrast ◽  
Cultured Cells ◽  
Light And Electron Microscopy ◽  
Cytoplasmic Inclusion ◽  
Electron Microscopic ◽  
Secondary Spermatocyte ◽  
Living Mouse ◽  
Circular Contour

A prominent cytoplasmic inclusion present in living mouse primary spermatocytes has been observed by both light and electron microscopy. It began to form at prometaphase and continued to increase in thickness and length as the cells developed. By metaphase it was a distinct sausage-shaped boundary that enclosed a portion of the cytoplasm between the spindle and the cell membrane. At the end of metaphase, the inclusion reached its maximum length. At telophase, it was divided between the daughter secondaries. The inclusion persisted as a circular contour in the interphase secondary spermatocyte. Electron microscopy of the same cultured cells that were previously observed with light microscopy revealed that the inclusion was a distinctive formation of membranes. It consisted of agranular cisternae and vesicles, and was therefore a membranous complex. Many of the smaller vesicles in the membranous complex resembled those found in the spindle. The cisternae in the membranous complex were identical to the cisternal endoplasmic reticulum of interphase primary spermatocytes. Nevertheless, the organization of vesicles and cisternae into the membranous complex was unique for the primaries in division stages, since such an organization was not present in their interphase stages.

Anatomy of the Unpollinated and Pollinated Watermelon Stigma

1982 ◽  
Vol 54 (1) ◽  
pp. 341-355
Author(s):  
M. SEDGLEY
Keyword(s):  
Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Light And Electron Microscopy ◽  
Freeze Fracture ◽  
Pollen Grain ◽  
Acidic Polysaccharides ◽  
Before And After ◽  
Em Autoradiography ◽  
Pollen Grain Wall ◽  
Stigma Secretion

The structure of the watermelon stigma before and after pollination was studied using light and electron microscopy, freeze-fracture and autoradiography. The wall thickenings of the papilla transfer cells contained callose and their presence prior to pollination was confirmed using EM-autoradiography, freeze-fracture and fixation. No further callose thickenings were produced following pollination. Pollination resulted in a rapid increase in aqueous stigma secretion and localized disruption of the cuticle, which appeared to remain on the surface of the secretion. Autolysis of the papilla cells, which had commenced prior to pollination, was accelerated and appeared to take place via cup-shaped vacuoles developed from distended endoplasmic reticulum. The reaction was localized to the papilla cells adjacent to the pollen tube only. Both pollen-grain wall and stigma secretion contained proteins, carbohydrates, acidic polysaccharides, lipids and phenolics.

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