The Structure of Sycamore Callus Cells During Division in a Partially Synchronized Suspension Culture

1970 ◽  
Vol 6 (2) ◽  
pp. 299-321
Author(s):  
K. ROBERTS ◽  
D. H. NORTHCOTE
Keyword(s):  
Cell Wall ◽  
Electron Microscope ◽  
Cell Plate ◽  
Optical Microscope ◽  
The Other ◽  
Active Movement ◽  
Developmental Sequence ◽  
Golgi Bodies ◽  
Dividing Cells ◽  
Peripheral Cytoplasm

Sycamore suspension callus cells have been partially synchronized to give a culture with a mitotic index of 15%. Living dividing cells of the culture have been examined with Nomarski differential interference optics and a comparable study made on fixed cells with the electron microscope. An organized band of reticulate cytoplasm partially encircles the nucleus at mitosis. The cell divides by the formation of a phragmosome which grows across the large vacuole; this allows the organization of the cytoplasm which forms the cell plate to be examined separately from the more general cytoplasm of the cell. The cell plate grows from one side of the cell to the other and down its length a complete developmental sequence can be seen. The Golgi bodies and the endoplasmic reticulum are probably involved in the formation of material for the construction of the cell plate and young cell wall. Microfibrils are formed within the plate in the more mature regions, while material contained within vesicles is incorporated at the young growing edge. At the edge of the plate microtubules are found and these correspond to the fibrillar appearance of the phragmoplast seen with the optical microscope. In the living cell an active movement of organelles along the peripheral cytoplasm can be seen and with fixed cells viewed with the electron microscope microtubules are often found adjacent to the plasmalemma and lying close to mitochondria, crystal-containing bodies and plastids. The appearance of crystal-containing bodies and plastids containing phytoferritin is described.

scholarly journals THE CYTOPLASMIC FINE STRUCTURE OF THE DIATOM, NITZSCHIA PALEA

1963 ◽  
Vol 18 (2) ◽  
pp. 429-440 ◽  
Author(s):  
Ryan W. Drum
Keyword(s):  
Cell Wall ◽  
Fine Structure ◽  
Electron Microscope ◽  
Hydrofluoric Acid ◽  
Oil Bodies ◽  
Oil Droplets ◽  
Pennate Diatom ◽  
Thin Sections ◽  
Nitzschia Palea ◽  
Peripheral Cytoplasm

The cytoplasmic fine structure of the motile, pennate diatom, Nitzschia palea was studied in thin sections viewed in the electron microscope. The cells were fixed in OsO4, embedded in methacrylate, and immersed in 10 per cent hydrofluoric acid (HF) for 36 to 40 hours to remove the siliceous cell wall prior to sectioning. The HF treatment did not cause any obvious cytoplasmic damage. The dictyosome complex is perinuclear, and located only in the central cytoplasm. Mitochondria are sparse in the central cytoplasm, but abundant in the peripheral cytoplasm, and fill many of the transvacuolar cytoplasmic strands. Characteristic, amorphous oil bodies fill certain cytoplasmic strands and probably are not leucosin. The pyrenoid appears to be membrane limited, and oil droplets are found adjacent to the pyrenoid. The pyrenoid of another diatom, Cymbella affinis, is also membrane-limited. The membrane limiting the pyrenoid may be a composite of the terminal portions of chloroplast discs, facilitating rapid movement of photosynthate into the pyrenoid matrix, where the characteristic oil droplets may be formed. Carinal fibrils are found singly in each carinal pore, and may be involved in the locomotion of Nitzschia palea.

Influence of Microstructure and Precipitates on the Strength of Container Steel

2012 ◽  
Vol 586 ◽  
pp. 225-229
Author(s):  
Jia Yan Ma ◽  
Wen Liang ◽  
Rong Dong Han ◽  
Yun Guan ◽  
Zhao Jun Deng
Keyword(s):  
Electron Microscope ◽  
Scanning Electron Microscope ◽  
Transmission Electron Microscope ◽  
Optical Microscope ◽  
The Other ◽  
Precipitation Strengthening ◽  
Strengthening Effect ◽  
Transmission Electron ◽  
Uniform Dispersion ◽  
Scanning Electron

The variation rules of strength with the microstructure and precipitates of container steel were studied by optical microscope (OM), scanning electron microscope (SEM) and transmission electron microscope (TEM). The results show that the microstructures of four kinds of test steels are all bainite and M/A island, but the number and size of islands of M/A and precipitates exist obvious difference: two kinds of test steels have fewer precipitates and more M/A islands, however, the other two kinds of steels are on the contrary. As for the former two kinds steels, the number of M/A islands is larger, and the size is smaller, the strength of steel is higher; For the later two kinds steels, the number of precipitates less than 30nm is larger, and distribution is more uniform dispersion, the strength is higher, precipitation strengthening effect is better. Getting lots of small and uniform M/A islands or precipitates is an effective way of improving the performance of steel.

scholarly journals THE LABELING OF CULTURED CELLS OF ACER WITH [14C]PROLINE AND ITS SIGNIFICANCE

1974 ◽  
Vol 60 (3) ◽  
pp. 695-701 ◽  
Author(s):  
F. C. Steward ◽  
H. W. Israel ◽  
M. M. Salpeter
Keyword(s):  
Cell Wall ◽  
Electron Microscope ◽  
Cell Walls ◽  
Cultured Cells ◽  
The State ◽  
The Other ◽  
Electron Microscope Autoradiography ◽  
Cells In Culture ◽  
Microscope Autoradiography ◽  
The Status

The distribution of the radioactivity from [14C]proline that is bound in cultured cells of Acer has been determined by electron microscope autoradiography. In this way proline may be related to the cell wall as a morphological entity rather than as a fraction in a biochemical separation of a heterogeneous crop of cells. The cells in culture may vary greatly. Some are active growing, turgid cells, with thin protoplasts tightly pressed against their walls; in others the protoplasts may spontaneously withdraw from the wall; in still others the protoplasts disorganize, and walls thicken and become sculptured as the cells differentiate and even senesce. Different culturing practices may affect the status of the cells, and this, in turn, affects the distribution of radioactivity from proline in the cells. Cells which are actively growing, turgid, and nucleated have the highest grain density in their protoplasts and nuclei; as the protoplasts of such cells withdraw from their walls, they retain the bulk of the radioactivity. On the other hand, in cells which have thickened walls and sparse protoplast contents, the radioactivity is accumulated in their walls. A high content of proline and hydroxyproline-rich protein is, therefore, not a necessary or invariable feature of the cell walls of cultured Acer cells but depends on the state of development of these cells.

scholarly journals Ultrastructure of Lejeunea spp. leaves surface in a lowland tropical urban forest of Universitas Indonesia Campus, Depok, Indonesia

2020 ◽  
Vol 21 (9) ◽  
Author(s):  
Afiatry Putrika ◽  
Dhita Mutiara Nabella ◽  
Andi Salamah ◽  
Nisyawati NISYAWATI ◽  
Astari Dwiranti
Keyword(s):  
Cell Wall ◽  
Electron Microscope ◽  
Cell Surface ◽  
Light Microscope ◽  
Urban Forest ◽  
Wide Distribution ◽  
The Other ◽  
Wall Surface ◽  
The World ◽  
Scanning Electron

Abstract. Putrika A, Nabella DM, Salamah A, Nisyawati, Dwiranti A. 2020. Ultrastructure of Lejeunea spp. leaves surface in a lowland tropical urban forest of Universitas Indonesia Campus, Depok, Indonesia. Biodiversitas 21: 4184-4191. Lejeunea is one of liverworts genera that have a wide distribution in the world. It has many variations of the character that have not been revealed, such as variations of the cell surface. The purpose of this research was to study the ultrastructure of Lejeunea spp. leaves surface in a lowland tropical urban forest of Universitas Indonesia (UI) Campus, Depok, Indonesia. Six species of Lejeunea spp. were studied, i.e., L. anisophylla, L. cocoes, L. exilis, L. papilionacea, L. catanduana, and L. curviloba. The research methods carried out in this study consisted of the sample observation using a light microscope, sample preparation for Scanning Electron Microscope (SEM) observation (fixation, post-fixation, dehydration, drying, mounting), and observations using SEM. The results of observation using a light microscope showed the smooth cell surface of all samples studied. Meanwhile, the differences between six species of Lejeunea in the UI campus could be differentiated under SEM. L. catanduana could be distinguished from other species from its cell wall thickness and texture, ornamentation types, and the number of ornamentations per cell. The texture of the cell wall of L. catanduana was the roughest than the other species due to abundant ornamentation such as papillae on its the cell wall surface. Furthermore, only this species has mamillae on the cell surface. The number of papillae or mamillae was 1-4 per cell. On the other hand, L. cocoes has the thinnest cell wall and slightly rough texture. Only this species has the simple papillae on the cell surface. Thus, the results of this study suggested that the cell surface variations in Lejeunea might be potential to be used as taxonomic characters in grouping species.

The Alteration of the Pore Spaces in Sandstones

1973 ◽  
Vol 31 ◽  
pp. 210-211
Author(s):  
R. E. Ferrell ◽  
G. G. Paulson
Keyword(s):  
Electron Microscope ◽  
Scanning Electron Microscope ◽  
The Other ◽  
Coarse Grained ◽  
Depositional Fabric ◽  
Soluble Components ◽  
Scanning Electron ◽  
Shape And Size

The pore spaces in sandstones are the result of the original depositional fabric and the degree of post-depositional alteration that the rock has experienced. The largest pore volumes are present in coarse-grained, well-sorted materials with high sphericity. The chief mechanisms which alter the shape and size of the pores are precipitation of cementing agents and the dissolution of soluble components. Each process may operate alone or in combination with the other, or there may be several generations of cementation and solution.The scanning electron microscope has ‘been used in this study to reveal the morphology of the pore spaces in a variety of moderate porosity, orthoquartzites.

Freeze-Fracture Replication in the Ultrastructure of Blue-Green Algae

1967 ◽  
Vol 25 ◽  
pp. 74-75
Author(s):  
L. V. Leak
Keyword(s):  
Cell Wall ◽  
Electron Microscope ◽  
Green Algae ◽  
Three Dimensional ◽  
Freeze Fracture ◽  
Electron Microscopic ◽  
Photosynthetic Membranes ◽  
Blue Green Algae ◽  
Cell Biol ◽  
Cellular Components

Electron microscopic observations of freeze-fracture replicas of Anabaena cells obtained by the procedures described by Bullivant and Ames (J. Cell Biol., 1966) indicate that the frozen cells are fractured in many different planes. This fracturing or cleaving along various planes allows one to gain a three dimensional relation of the cellular components as a result of such a manipulation. When replicas that are obtained by the freeze-fracture method are observed in the electron microscope, cross fractures of the cell wall and membranes that comprise the photosynthetic lamellae are apparent as demonstrated in Figures 1 & 2.A large portion of the Anabaena cell is composed of undulating layers of cytoplasm that are bounded by unit membranes that comprise the photosynthetic membranes. The adjoining layers of cytoplasm are closely apposed to each other to form the photosynthetic lamellae. Occassionally the adjacent layers of cytoplasm are separated by an interspace that may vary in widths of up to several 100 mu to form intralamellar vesicles.

Sites of Adsorption of the Bacteriophages T3 and T5 on the Wall of Escherichia Coli B.

1967 ◽  
Vol 25 ◽  
pp. 96-97
Author(s):  
Manfred E. Bayer
Keyword(s):  
Escherichia Coli ◽  
Cell Wall ◽  
Electron Microscope ◽  
Uranyl Acetate ◽  
E Coli ◽  
Receptor Sites ◽  
Rigid Cell Wall ◽  
Host Cell Surface ◽  
Bacterial Viruses ◽  
Escherichia Coli B

Bacterial viruses adsorb specifically to receptors on the host cell surface. Although the chemical composition of some of the cell wall receptors for bacteriophages of the T-series has been described and the number of receptor sites has been estimated to be 150 to 300 per E. coli cell, the localization of the sites on the bacterial wall has been unknown.When logarithmically growing cells of E. coli are transferred into a medium containing 20% sucrose, the cells plasmolize: the protoplast shrinks and becomes separated from the somewhat rigid cell wall. When these cells are fixed in 8% Formaldehyde, post-fixed in OsO4/uranyl acetate, embedded in Vestopal W, then cut in an ultramicrotome and observed with the electron microscope, the separation of protoplast and wall becomes clearly visible, (Fig. 1, 2). At a number of locations however, the protoplasmic membrane adheres to the wall even under the considerable pull of the shrinking protoplast. Thus numerous connecting bridges are maintained between protoplast and cell wall. Estimations of the total number of such wall/membrane associations yield a number of about 300 per cell.

Development of 200 kV Scanning-Transmission Electron Microscope

1974 ◽  
Vol 32 ◽  
pp. 410-411
Author(s):  
H. Koike ◽  
S. Sakurai ◽  
K. Ueno ◽  
M. Watanabe
Keyword(s):  
Electron Microscopy ◽  
Electron Microscope ◽  
Scanning Transmission Electron Microscope ◽  
The Other ◽  
Morphological Observation ◽  
Magnetic Domains ◽  
Transmission Electron ◽  
Scanning Transmission ◽  
Backscattered Electron ◽  
Increasing Demand

In recent years, there has been increasing demand for higher voltage SEMs, in the field of surface observation, especially that of magnetic domains, dislocations, and electron channeling patterns by backscattered electron microscopy. On the other hand, the resolution of the CTEM has now reached 1 ∼ 2Å, and several reports have recently been made on the observation of atom images, indicating that the ultimate goal of morphological observation has beem nearly achieved.

Reconstruction of electron holograms recorded in a non-FEG, non-biprism TEM

1995 ◽  
Vol 53 ◽  
pp. 618-619
Author(s):  
Z.L. Wang
Keyword(s):  
Electron Microscope ◽  
Single Crystal ◽  
Experimental Technique ◽  
Transmission Electron Microscope ◽  
The Other ◽  
Electron Holography ◽  
Transmission Electron ◽  
Coherent Sources ◽  
Imaging Theory ◽  
Normal Specimen

An experimental technique for performing electron holography using a non-FEG, non-biprism transmission electron microscope (TEM) has been introduced by Ru et al. A double stacked specimens, one being a single crystal foil and the other the specimen, are loaded in the normal specimen position in TEM. The single crystal, which is placed onto the specimen, is responsible to produce two beams that are equivalent to two virtual coherent sources illuminating the specimen beneath, thus, permitting electron holography of the specimen. In this paper, the imaging theory of this technique is described. Procedures are introduced for digitally reconstructing the holograms.

Electron microscope studies of the plastic deformation of ternary alloys based on GaAs

1990 ◽  
Vol 48 (4) ◽  
pp. 1120-1120
Author(s):  
R. Haswell ◽  
U. Bangert ◽  
P. Charsley
Keyword(s):  
Plastic Deformation ◽  
Electron Microscope ◽  
Room Temperature ◽  
Stacking Faults ◽  
The Other ◽  
Ternary Alloys ◽  
Dislocation Mobility ◽  
Semiconducting Materials ◽  
Micro Indentation

A knowledge of the behaviour of dislocations in semiconducting materials is essential to the understanding of devices which use them . This work is concerned with dislocations in alloys related to the semiconductor GaAs . Previous work on GaAs has shown that microtwinning occurs on one of the <110> rosette arms after indentation in preference to the other . We have shown that the effect of replacing some of the Ga atoms by Al results in microtwinning in both of the rosette arms.In the work to be reported dislocations in specimens of different compositions of Gax Al(1-x) As and Gax In(1-x) As have been studied by using micro indentation on a (001) face at room temperature . A range of electron microscope techniques have been used to investigate the type of dislocations and stacking faults/microtwins in the rosette arms , which are parallel to the [110] and [10] , as a function of composition for both alloys . Under certain conditions microtwinning occurs in both directions . This will be discussed in terms of the dislocation mobility.

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