Ultrastructure and cleavage of chlamydospore chains of Thielaviopsis basicola

1970 ◽  
Vol 48 (12) ◽  
pp. 2305-2308 ◽  
Author(s):  
Christos Christias ◽  
Kenneth F. Baker
Keyword(s):  
Thin Film ◽  
Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Germ Tube ◽  
Outer Region ◽  
Thielaviopsis Basicola ◽  
Thin Electron ◽  
Ultra Thin Section ◽  
Inner Region ◽  
Septal Pores

Electron microscopy revealed that numerous spherical or ellipsoidal globules of reserve nutrient material fill the chlamydospore cells, with cytoplasm as a thin film between these globules. The basal cell of the chain is not a chlamydospore; it is filled with cytoplasm and does not contain these globules. Its plasma membrane, nucleus, mitochondria, lomasomes, and endoplasmic reticulum are evident in ultra-thin section. The walls of chlamydospore cells are thick and without distinct layers, except for an electron-dense outer region and a more electron-transparent inner region. Chlamydospore cells in the chain are separated by a very thin electron-transparent binding layer. A thin two-layered envelope surrounds the entire chain. When chlamydospore chains are treated with chitinase, this envelope remains attached around single separated cells, rather than dissolving away. Cytoplasm of cells in the chain is continuous through septal pores. The end walls of the cells become the opercula after the cells are freed from the chain. The germ tube always emerges at the side where the operculum opens, never through the septal pore.

Nematode morphogenesis: fine structure of the cuticle of each stage of the nematode, Panagrellus silusiae (de Man 1913) Goodey 1945

1968 ◽  
Vol 46 (5) ◽  
pp. 1019-1022 ◽  
Author(s):  
M. R. Samoiloff ◽  
J. Pasternak
Keyword(s):  
Endoplasmic Reticulum ◽  
Fine Structure ◽  
Outer Region ◽  
Free Living ◽  
Larval Stages ◽  
Transparent Layer ◽  
Layer 2 ◽  
Free Living Nematode ◽  
Inner Region ◽  
De Man

The fine structure of the cuticle of each of the five stages of the free-living nematode Panagrellus silusiae (de Man 1913) Goodey 1945 has been examined. The cuticle plan is made up of a few regions: (1) an outer region (~350 Å) which consists of three layers: a thin outer layer, an electron transparent layer, and a thin but diffuse inner layer; (2) an inner region which has virtually no resolvable substructure other than a striated layer. This layer is not usually seen in the early stages of development but is readily apparent in the L4 and adult stages. The pattern of the cuticle is the same for each stage.The lateral fields—alae—reveal a definite differentiation during the life cycle; in the larval stages they are mere bulges but in the adults they take on a distinct four-lobed shape. The cuticle lining the pharynx consists of two regions, and there is never a striated band present nor does the cuticle increase in width during nematode growth.The interchordal hypodermis is devoid of endoplasmic reticulum, Golgi material, and mitochondria, but in some regions glycogen is found.

Ultrastructure of basidiospore germination in Fomes fomentarius

1978 ◽  
Vol 56 (22) ◽  
pp. 2865-2872 ◽  
Author(s):  
Ichiko Tsuneda ◽  
Lorene L. Kennedy
Keyword(s):  
Endoplasmic Reticulum ◽  
Cell Wall ◽  
Germ Tube ◽  
Early Stage ◽  
Dense Layer ◽  
Lipid Bodies ◽  
Fomes Fomentarius ◽  
Additional Cell ◽  
Thin Electron ◽  
Germ Tubes

Germination of basidiospores in Fomes fomentarius (Fries) Kickx is bipolar with germ tubes emerging at both ends. Ungerminated spores are smooth with a thick cell wall consisting of two layers: an outer thin, electron-dense layer and an inner thick, electron-light layer. During the early stage of germination, two additional cell wall layers are formed: a very thin, electron-dense layer and a relatively thick, electron-light layer. Germ tube walls originate from these newly formed, inner layers. Ungerminated spores are uninucleate and contain numerous lipid bodies, ribosomes, and cisternae of endoplasmic reticulum. Germinated spores have distinct mitochondria and an invaginated plasma membrane and are usually devoid of endoplasmic reticulum.

Studies on Dracunculus medinensis (Linnaeus) III. Structure of the Phasmids in the First-Stage Larva

1973 ◽  
Vol 47 (1) ◽  
pp. 27-33 ◽  
Author(s):  
R. Muller ◽  
D.S. Ellis
Keyword(s):  
Endoplasmic Reticulum ◽  
Single Cell ◽  
Outer Region ◽  
Stage Larva ◽  
Lateral Nerve ◽  
Acid Mucopolysaccharides ◽  
Nerve Bundles ◽  
Inner Region

The phasmids of the first-stage larva of Dracunculus medinensis were paired, each consisting of a single cell with a lumen connected to the exterior by a closable duct. The cell consisted of an outer region filled with mitochondria and an inner region consisting of endoplasmic reticulum bordering the lumen, whose inner surfaces was supported by a fibrillar framework. There were a pair of cilia projecting into the lumen of each cell and two nerve bundles at the base in direct continuity with a branch of the lateral nerve. The lumen of the phasmidial cell contained acid mucopolysaccharides and esterases.

scholarly journals SPERMIOGENESIS IN CANCER CRABS

1969 ◽  
Vol 43 (3) ◽  
pp. 575-603 ◽  
Author(s):  
Susan G. Langreth
Keyword(s):  
Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Nucleic Acid ◽  
Sperm Cell ◽  
Periodic Acid ◽  
Light And Electron Microscopy ◽  
Mature Sperm ◽  
Periodic Acid Schiff ◽  
The Core ◽  
Inner Region

Spermiogenesis in Cancer crabs was studied by light and electron microscopy. The sperm are aflagellate, and when mature consist primarily of a spherical acrosome surrounded by the nucleus with its short radiating arms. The acrosome forms by a coalescence of periodic acid-Schiff-positive (PAS-positive) vesicles. During spermiogenesis one edge of the acrosomal vesicle invaginates to form a PAS-negative central core. The inner region of the acrosome bounding the core contains basic proteins which are not complexed to nucleic acid. The formation of an elaborate lattice-like complex of fused membranes, principally from membranes of the endoplasmic reticulum, is described. These membranes are later taken into the nucleus and subsequently degenerate. In late spermatids, when most of the cytoplasm is sloughed, the nuclear envelope and the cell membrane apparently fuse to become the limiting boundary over most of the sperm cell. In the mature sperm the chromatin of the nucleus and arms, which is Feulgen-positive, contains no detectable protein. The chromatin filaments appear clumped, branched, and anastomosed; morphologically, they resemble the DNA of bacterial nuclei. Mitochondria are absent or degenerate in mature sperm of Cancer crabs, but the centrioles persist in the nucleoplasm at the base of the acrosome.

Morphological studies of N-acetylglucosamine induced germ tube formation by Candida albicans

1985 ◽  
Vol 31 (8) ◽  
pp. 696-701 ◽  
Author(s):  
Michael J. Hubbard ◽  
Patrick A. Sullivan ◽  
Maxwell G. Shepherd
Keyword(s):  
Candida Albicans ◽  
Germ Tube ◽  
Ultrathin Section ◽  
Outer Region ◽  
Tube Formation ◽  
Morphological Studies ◽  
Transmission Electron ◽  
Thin Electron ◽  
Germ Tubes ◽  
Electron Lucent

In N-acetylglucosamine induced germ tube formation by Candida albicans, multiple (up to five) protuberances appeared within 90 min at 37 °C on each yeast cell. The protuberances were extensions of the cytosol and contained vesiclelike structures. Usually only one protuberance subsequently developed into a germ tube. The germ tubes emanated from all aspects of the cell surface but seldom from the budding (long axis) poles. Pseudohyphae, which originated from the budding pole, exhibited a marked constriction at the site of emergence and were 0.6–2.5 μm in diameter compared with a diameter of 0.6–0.8 μm for germ tubes. The presence of septa confirmed that germ tubes are precursors of septate mycelia. Ultrathin-section transmission electron microscopy of aldehyde plus osmium fixed cells revealed electron-lucent walls with a thin electron-dense outer layer. A fibrillar border was also routinely associated with germ tubes. Poststaining with potassium permanganate revealed, in addition, a previously invisible fuzzy layer on the outer region of the cell wall which extended over bud scars and germ tubes and which coalesced at sites of contact between cells.

Modification of Pineal Ultrastructure by Exogenous Hormones

1967 ◽  
Vol 25 ◽  
pp. 170-171
Author(s):  
R. A. Turner ◽  
A. E. Rodin ◽  
D. K. Roberts
Keyword(s):  
Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Rough Endoplasmic Reticulum ◽  
Estradiol Benzoate ◽  
Female Rats ◽  
List Type ◽  
Type Number ◽  
Pregnant Rats ◽  
Gonadal Atrophy ◽  
Pineal Ultrastructure

There have been many reports which establish a relationship between the pineal and sexual structures, including gonadal hypertrophy after pinealectomy, and gonadal atrophy after injection of pineal homogenates or of melatonin. In order to further delineate this relationship the pineals from 5 groups of female rats were studied by electron microscopy:ControlsPregnant ratsAfter 4 weekly injections of 0.1 mg. estradiol benzoate.After 8 daily injections of 150 mcgm. melatonin (pineal hormone).After 8 daily injections of 3 mg. serotonin (melatonin precursor).No ultrastructural differences were evident between the control, and the pregnancy and melatonin groups. However, the estradiol injected animals exhibited a marked increase in the amount and size of rough endoplasmic reticulum within the pineal cells.

Copper Localization in Cirrhotic Rat Liver by Scanning Electron Microscopy

1969 ◽  
Vol 27 ◽  
pp. 38-39 ◽  
Author(s):  
J. C. Russ ◽  
E. McNatt
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Electron Microscope ◽  
Copper Acetate ◽  
Lead Citrate ◽  
Dense Bodies ◽  
Transmission Electron ◽  
Electron Mode ◽  
Scanning Electron

In order to study the retention of copper in cirrhotic liver, rats were made cirrhotic by carbon tetrachloride inhalation twice weekly for three months and fed 0.2% copper acetate ad libidum in drinking water for one month. The liver tissue was fixed in osmium, sectioned approximately 2000 Å thick, and stained with lead citrate. The section was examined in a scanning electron microscope (JEOLCO JSM-2) in the transmission electron mode.Figure 1 shows a typical area that includes a red blood cell in a sinusoid, a disse, and a portion of the cytoplasm of a hepatocyte which contains several mitochondria, peribiliary dense bodies, glycogen granules, and endoplasmic reticulum.

Morphological and biochemical analyses of changes in rat hepatocytes related to wine and ethanol consumption

1984 ◽  
Vol 42 ◽  
pp. 232-233
Author(s):  
S.M. Geyer ◽  
C.L. Mendenhall ◽  
J.T. Hung ◽  
E.L. Cardell ◽  
R.L. Drake ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Enzyme Activity ◽  
Malic Enzyme ◽  
Smooth Endoplasmic Reticulum ◽  
Rat Hepatocytes ◽  
Mature Male ◽  
Treatment Groups ◽  
Malic Enzyme Activity ◽  
Biochemical Analyses

Thirty-three mature male Holtzman rats were randomly placed in 3 treatment groups: Controls (C); Ethanolics (E); and Wine drinkers (W). The animals were fed synthetic diets (Lieber type) with ethanol or wine substituted isocalorically for carbohydrates in the diet of E and W groups, respectively. W received a volume of wine which provided the same gram quantity of alcohol consumed by E. The animals were sacrificed by decapitation after 6 weeks and the livers processed for quantitative triglycerides (T3), proteins, malic enzyme activity (MEA), light microscopy (LM) and electron microscopy (EM). Morphometric analysis of randomly selected LM and EM micrographs was performed to determine organellar changes in centrilobular (CV) and periportal (PV) regions of the liver. This analysis (Table 1) showed that hepatocytes from E were larger than those in C and W groups. Smooth endoplasmic reticulum decreased in E and increased in W compared to C values.

Triple Fixation For Electron Microscopy

1968 ◽  
Vol 26 ◽  
pp. 90-91 ◽  
Author(s):  
M. A. Hayat
Keyword(s):  
Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Electron Beam ◽  
Plasma Membrane ◽  
Myelin Sheath ◽  
Good Deal ◽  
Granular Structure ◽  
Oxidizing Agent ◽  
Fixation Technique ◽  
Large Clusters

Potassium permanganate has been successfully employed to study membranous structures such as endoplasmic reticulum, Golgi, plastids, plasma membrane and myelin sheath. Since KMnO4 is a strong oxidizing agent, deposition of manganese or its oxides account for some of the observed contrast in the lipoprotein membranes, but a good deal of it is due to the removal of background proteins either by dehydration agents or by volatalization under the electron beam. Tissues fixed with KMnO4 exhibit somewhat granular structure because of the deposition of large clusters of stain molecules. The gross arrangement of membranes can also be modified. Since the aim of a good fixation technique is to preserve satisfactorily the cell as a whole and not the best preservation of only a small part of it, a combination of a mixture of glutaraldehyde and acrolein to obtain general preservation and KMnO4 to enhance contrast was employed to fix plant embryos, green algae and fungi.

Transmission Electron Microscopy of oriented Co84Cr14Ta2 thin films for longitudinal magnetic recording

1991 ◽  
Vol 49 ◽  
pp. 756-757
Author(s):  
T. P. Nolan
Keyword(s):  
Thin Film ◽  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Low Cost ◽  
Low Noise ◽  
Information Storage ◽  
High Coercivity ◽  
Magnetic Alloy ◽  
Magnetic Media ◽  
Transmission Electron

Thin film magnetic media are being used as low cost, high density forms of information storage. The development of this technology requires the study, at the sub-micron level, of morphological, crystallographic, and magnetic properties, throughout the depth of the deposited films. As the microstructure becomes increasingly fine, widi grain sizes approaching 100Å, the unique characterization capabilities of transmission electron microscopy (TEM) have become indispensable to the analysis of such thin film magnetic media.Films were deposited at 225°C, on two NiP plated Al substrates, one polished, and one circumferentially textured with a mean roughness of 55Å. Three layers, a 750Å chromium underlayer, a 600Å layer of magnetic alloy of composition Co84Cr14Ta2, and a 300Å amorphous carbon overcoat were then sputter deposited using a dc magnetron system at a power of 1kW, in a chamber evacuated below 10-6 torr and filled to 12μm Ar pressure. The textured medium is presently used in industry owing to its high coercivity, Hc, and relatively low noise. One important feature is that the coercivity in the circumferential read/write direction is significandy higher than that in the radial direction.

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