scholarly journals Ultrastructure of the Developing Aleurone Cells of Wheat Grain

1963 ◽  
Vol 16 (4) ◽  
pp. 768 ◽  
Author(s):  
MS Buttrose
Keyword(s):  
Electron Microscopy ◽  
Light Microscopy ◽  
Cell Walls ◽  
Osmium Tetroxide ◽  
Aleurone Layer ◽  
Wheat Grain ◽  
Aleurone Cells ◽  
Wheat Kernel ◽  
Large Numbers ◽  
Inner Surface

The developing aleurone layer cells of the wheat kernel have been investigated by electron microscopy and the results compared with those of light microscopy. Two weeks after flowering vacuoles appear in the cells and deposits accumulate in these until maturity when the cells are filled 'with the resulting "vacuolar units" 2-3p. in diameter, corresponding to the aleurone grains of light microscopy. The wheat aleurone grain consists of a bounding membrane (of vacuole origin) enclosing a matrix in which are embedded spherical deposits. Some of these deposits are translucent and others opaque to electrons after potassium permanganate and osmium tetroxide fixation. At all stages examined the cytoplasm of aleurone cells contained large numbers of small unidentified bodies with irregular outline and dense contents. At first they are dispersed, but towards maturity are organized as a monolayer over the surface of each aleurone grain and the inner surface of the cell walls. The apparent specificity of these structures to aleurone cells is discussed in relation to future chemical and physiological studies of the tissue.

Ectodesmata as Revealed By Freeze-Etch Preparations of Plant Epidermal Cell Walls

1973 ◽  
Vol 31 ◽  
pp. 468-469
Author(s):  
N.C. Lyon ◽  
W. C. Mueller
Keyword(s):  
Electron Microscopy ◽  
Acetic Acid ◽  
Nitric Acid ◽  
Oxalic Acid ◽  
Light Microscopy ◽  
Epidermal Cell ◽  
Cell Walls ◽  
Plant Viruses ◽  
Plant Leaves ◽  
Thin Sections

Schumacher and Halbsguth first demonstrated ectodesmata as pores or channels in the epidermal cell walls in haustoria of Cuscuta odorata L. by light microscopy in tissues fixed in a sublimate fixative (30% ethyl alcohol, 30 ml:glacial acetic acid, 10 ml: 65% nitric acid, 1 ml: 40% formaldehyde, 5 ml: oxalic acid, 2 g: mecuric chloride to saturation 2-3 g). Other workers have published electron micrographs of structures transversing the outer epidermal cell in thin sections of plant leaves that have been interpreted as ectodesmata. Such structures are evident following treatment with Hg++ or Ag+ salts and are only rarely observed by electron microscopy. If ectodesmata exist without such treatment, and are not artefacts, they would afford natural pathways of entry for applied foliar solutions and plant viruses.

Selective Sampling and Orientation of Non-Homogeneous Tissues

1968 ◽  
Vol 26 ◽  
pp. 98-99
Author(s):  
C. C. Clawson ◽  
L. W. Anderson ◽  
R. A. Good
Keyword(s):  
Electron Microscopy ◽  
Electron Microscope ◽  
Light Microscopy ◽  
Random Sampling ◽  
New Method ◽  
Microscope Examination ◽  
Small Areas ◽  
Selective Sampling ◽  
Large Numbers ◽  
Specific Orientation

Investigations which require electron microscope examination of a few specific areas of non-homogeneous tissues make random sampling of small blocks an inefficient and unrewarding procedure. Therefore, several investigators have devised methods which allow obtaining sample blocks for electron microscopy from region of tissue previously identified by light microscopy of present here techniques which make possible: 1) sampling tissue for electron microscopy from selected areas previously identified by light microscopy of relatively large pieces of tissue; 2) dehydration and embedding large numbers of individually identified blocks while keeping each one separate; 3) a new method of maintaining specific orientation of blocks during embedding; 4) special light microscopic staining or fluorescent procedures and electron microscopy on immediately adjacent small areas of tissue.

scholarly journals Anatomía de la semilla de Tigridia pavonia (Iridaceae)

2017 ◽  
pp. 66
Author(s):  
Aída Carrillo-Ocampo ◽  
E.M. Engleman
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Light Microscopy ◽  
Thin Layer ◽  
Cell Walls ◽  
Histochemical Staining ◽  
Stage Of Development ◽  
Scanning Electron

With methods of light microscopy, histochemical staining and scanning electron microscopy, it was found that the ovule in the seed of Tigridia pavonia (Iridaceae) is anatropous, bitegmic, and crassinucellate. During development, the exotegmen is crushed and the endotegmen persists with tannins in the lumens and in the walls, which also react positively for lignin. The exotesta contains tannins and its outer walls are convex, thickened, and cuticularized. The mesotesta has multiple layers, accumulates abundant lipids, and forms a bulge in the chalaza. The cell walls of the endotesta collapse and accumulate tannins. In the chalaza, a hypostasal cushion contains tannins in the lumens and in the walls, which also react positively for lignin. At the micropylar end of the seed there is an operculum which consists of: a) a slightly crushed exotegmen, b) an endotegmen with cuticular thickenings that are concentric with respect to the micropyle, c) hemispherical deposists of cutin on the anticlinal walls of the endotegmen, and c) a thin layer of endosperm that covers the radicle. During its cellular stage of development, the endosperm has conspicuous transfer walls at the chalazal end next to the nucella. The embryo is small and has a conical cotyledon.

Colonization of Sphagnum cells by Lyophyllum palustre

1985 ◽  
Vol 63 (4) ◽  
pp. 757-761 ◽  
Author(s):  
E. Untiedt ◽  
K. Müller
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Light Microscopy ◽  
Host Cell ◽  
Cell Walls ◽  
Transmission Electron ◽  
Scanning Electron

Lyophyllum palustre (Peck) Singer, a basidiomycete (Tricholomataceae) parasitizing Sphagnum, was examined for points of contact between hyphae and Sphagnum cells with the help of light microscopy, scanning electron microscopy, and transmission electron microscopy. Results indicate that the fungus attacks Sphagnum cells by penetrating cell walls and altering host cell protosplasm. In addition, the formation of additional partitioning cell walls in attacked living Sphagnum cells was observed.

The development of the aleurone layer in canola (Brassica napus)

1993 ◽  
Vol 71 (9) ◽  
pp. 1193-1201 ◽  
Author(s):  
Edwin P. Groot ◽  
Lawrence A. Van Caeseele
Keyword(s):  
Image Analysis ◽  
Electron Microscope ◽  
Brassica Napus ◽  
Cell Walls ◽  
Cell Layer ◽  
Aleurone Layer ◽  
Electron Microscopic ◽  
Aleurone Cells ◽  
Mature Seeds ◽  
Microscopic Techniques

The presence of the aleurone layer in developing seeds of Brassica napus becomes apparent about 22 days after pollination when examined with light and electron microscopic techniques. Prior to aleurone differentiation, the endosperm cellularizes centripetally to form characteristic columns of cells. The pigmented cell layer of the inner integument, which is present in dark-hulled seeds of Brassica, is just external to the aleurone. The first characteristic structures that become apparent inside the aleurone are spherosomes formed by the coalescence of small oil droplets. Shortly thereafter, the cell walls of the aleurone become markedly thickened relative to the surrounding cells. The aleurone cells of mature seeds contain lipid and protein reserves but lack starch. Development of the aleurone layer occurs first near the adaxial area and proceeds until the micropylar area finally differentiates. Endosperm chloroplasts have a characteristic lens shape when viewed in section with the electron microscope. They appear to congregate around a nucleus along with a small amount of cytoplasm causing an astroid-shaped aggregation of cytoplasm in the majority of endosperm cells but only transiently in the aleurone. DNA fluorometry and image analysis showed that aleurone nuclei are triploid; therefore the aleurone layer is derived from the endosperm. Key words: aleurone layer, endosperm, seed development, ploidy, anatomy, Brassica napus.

scholarly journals PHYSICAL STUDIES OF PHOSPHOLIPIDS

1966 ◽  
Vol 30 (1) ◽  
pp. 1-11 ◽  
Author(s):  
D. Chapman ◽  
D. J. Fluck
Keyword(s):  
Electron Microscopy ◽  
Thermal Analysis ◽  
Differential Thermal Analysis ◽  
Transition Temperature ◽  
Light Microscopy ◽  
Osmium Tetroxide ◽  
Negative Staining ◽  
Hydrocarbon Chains ◽  
Myelin Figures

On heating pure, fully saturated 2,3-diacyl-DL-phosphatidyl-ethanolamines and 2,3-diacylphosphatidyl-cholines (lecithins) in water to the transition temperature at which large endothermic heat changes occur, they are observed, by light microscopy, to form myelin figures. This result is discussed in terms of the large difference in the transition temperature for "melting" of the hydrocarbon chains of unsaturated and saturated phospholipids and is illustrated by means of differential thermal analysis (D.T.A.) curves. These structures have been examined by electron microscopy after negative staining and after reaction with osmium tetroxide. Typical phospholipid lamella structures are seen in the phosphatidylcholines after negative staining, and in the phosphatidyl-ethanolamines after both negative staining and osmium fixation. The distances across these lamellae have been measured. Some preliminary investigations of the nature of the osmium tetroxide reaction with the phosphatidyl-ethanolamines have been made.

scholarly journals Electron-Microscopic Investigation of the Flora of Sheep Alimentary Tract

1970 ◽  
Vol 23 (4) ◽  
pp. 793 ◽  
Author(s):  
NJ Hoogenraad ◽  
FJR Hird
Keyword(s):  
Electron Microscopy ◽  
Small Intestine ◽  
Bacterial Cell ◽  
Cell Walls ◽  
Alimentary Tract ◽  
Microscopic Investigation ◽  
Electron Microscopic Investigation ◽  
Direct Examination ◽  
Electron Microscopic ◽  
Large Numbers

Digesta from different regions of the sheep alimentary tract have been examined using electron microscopy. Direct examination of digesta from the rumen has revealed the presence of a number of phages and of a large variety of bacteria differing considerably in their morphology. An atlas of electron micrographs of these bacteria has been presented. The presence of large numbers of bacterial cell walls ;n the rumen indicates that the breakdown of bacteria commences in this organ. The major sites of digestion of bacteria are in the abomasum and small intestine where there is a substantial removal and modification of bacteria.

Phytosterols in the aleurone layer of corn kernels

2000 ◽  
Vol 28 (6) ◽  
pp. 803-806 ◽  
Author(s):  
R. A. Moreau ◽  
V. Singh ◽  
A. Nuñez ◽  
K. B. Hicks
Keyword(s):  
Outer Layer ◽  
Cell Walls ◽  
Single Layer ◽  
Living Cells ◽  
Aleurone Layer ◽  
High Concentration ◽  
Aleurone Cells ◽  
Phytosterol Esters ◽  
Corn Fibre ◽  
Corn Kernels

Corn hulls are composed of two major layers: the outer layer, the pericarp, is made up of non-living cell walls, and an inner layer, the aleurone, consists of a single layer of living cells, surrounded by thick cell walls. Dissected pure pericarp and aleurone fractions were ground and extracted with hexane and the yields and compositions of the resulting oils were examined. This study revealed that the high levels of ferulate-phytosterol esters and the high concentration of sitostanol previously reported in corn-fibre oil actually originate in the aleurone cells.

Somatic mitosis in Erysiphe graminis hordei

1972 ◽  
Vol 18 (12) ◽  
pp. 1915-1922 ◽  
Author(s):  
W. E. McKeen
Keyword(s):  
Electron Microscopy ◽  
Light Microscopy ◽  
Nuclear Membrane ◽  
Osmium Tetroxide ◽  
Central Body ◽  
Nuclear Division ◽  
Light And Electron Microscopy ◽  
Erysiphe Graminis ◽  
The Other ◽  
Erysiphe Graminis Hordei

Somatic nuclear division in Erysiphe graminis hordei was studied by light and electron microscopy after various fixation and staining procedures. Electron microscopy studies of alcohol – acetic acid fixed material aided in providing an understanding of nuclear division and showing the gross alterations which occurred. Light microscopy indicated that a central body was always present at a specific site on the nuclear membrane in the interphase nucleus and was connected to chromatic spherical bodies. Microtubules were preserved when a short glutaraldehyde – osmium tetroxide fixation was used. Some microtubules extend from plaque to plaque while others terminate in kinetochores. A microtubular spindle, oblique to the nuclear and mildew-cells axes formed within the nuclear membrane. Typical prophases, metaphases, anaphases, and telophases were observed. Then one set of daughter chromatids bypassed the nucleolus which persisted intranuclearly until the daughter nuclei reached their destination, and the other set of daughter chromatids moved to midpoint in the other daughter cell. A narrow corridor, which connected daughter nuclei for some time, was filled mainly with microtubules and probably was the filament which was observed in the nucleus by light microscopy during nuclear division. At least six chromosomes were present in each nucleus.

Comparison of Scanning Electron Microscopy and Light Microscopy for the Diagnosis of Early Stages of Brown Rot Wood Decay

IAWA Journal ◽  
1993 ◽  
Vol 14 (3) ◽  
pp. 219-226 ◽  
Author(s):  
W. Wayne Wilcox
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Light Microscopy ◽  
Cell Walls ◽  
Wood Decay ◽  
Brown Rot ◽  
Early Stages ◽  
Polarised Light ◽  
Scanning Electron

As part of a larger study of the microscopical characteristics useful in diagnosing early stages of decay, an opportunity was created to compare the ability of light microscopy (LM) and scanning electron microscopy (SEM) to image these features. Although most features could be imaged by both technologies, imaging was much easier in the SEM because it was being used at the low end of its resolution and magnification capability while the LM was near the high end of its limitations. One important feature which could not be imaged in SEM was the earliest attack on the cell walls, a feature which was visible under polarised light in the LM.

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