The fine structure of Thioploca araucae and Thioploca chileae

1990 ◽  
Vol 36 (6) ◽  
pp. 438-448 ◽  
Author(s):  
Siegfried Maier ◽  
Horst Völker ◽  
Marita Beese ◽  
Victor A. Gallardo
Keyword(s):  
Electron Microscopy ◽  
Plasma Membrane ◽  
Fine Structure ◽  
Coastal Upwelling ◽  
The Other ◽  
Surface Topology ◽  
Cytoplasmic Material ◽  
Transmission Electron ◽  
Soft Bottoms ◽  
Sulfur Inclusions

Thioploca araucae and Thioploca chileae from the sublittoral soft bottoms of the coastal upwelling ecosystem off central Chile were examined by scanning and transmission electron microscopy. Except for filament diameter (30–43 and 12–20 μm, respectively) and slight differences in other dimensions and surface topology, the details of fine structure were essentially identical in the two species. The wall consisted of five layers, and only the inner layer was present in the septum. Multiple membrane intrusions dissected the procaryotic cytoplasmic material, which was restricted to a relatively thin layer within the wall. Sulfur inclusions and two other extracytoplasmic inclusions, as well as one kind of intracytoplasmic inclusion, were described. The central part of each cell consisted of one large vacuole, extending from septum to septum and representing a volume at least more than three times larger than the combined volume of wall and cytoplasm. The vacuole was separated from the other cell parts by a membrane. Electron-dense material was deposited between vacuole membrane and plasma membrane, between plasma membrane and wall, and inside membrane intrusions. A continuity between the vacuolar membrane and the other membranes was never encountered. The possible origin of such an extracytoplasmic membrane is discussed. Key words: benthos, electron microscopy, fine structure, Thioploca.

scholarly journals UNE FORME MICROTUBULAIRE ET PARACRISTALLINE DE RETICULUM ENDOPLASMIQUE DANS LES PHOTOCYTES DES ANNELIDES POLYNOINÆ

1966 ◽  
Vol 31 (1) ◽  
pp. 135-158 ◽  
Author(s):  
J. M. Bassot
Keyword(s):  
Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Plasma Membrane ◽  
Fine Structure ◽  
Nuclear Envelope ◽  
Contact Surface ◽  
Special Kind ◽  
The Other ◽  
Cytoplasmic Organelle ◽  
Specialized Form

Luminous cells of polynoid worm elytra have been examined by methods of electron microscopy, with special attention focused on the fine structure of photogenic grains. These cells send apical prolongations into the mid-part of the elytra. The plasma membrane is very sinuous, and a special kind of desmosome links two portions of the same membrane. In addition to all the organelles which can be found in nonluminescent epithelial cells of the elytra, numerous photogenic grains are contained in their cytoplasm. These grains are composed of undulating microtubules measuring 200 A in diameter; their disposition in the grain is highly regular, and the grains appear as paracrystals. At the borders of the grains, the walls of the microtubules are often in continuity with those of the endoplasmic reticulum and with the external membrane of the nuclear envelope. Because of this fact, the microtubules of the grains may be considered a cytoplasmic organelle, representing a specialized form of the endoplasmic reticulum. The microtubules permit the repartition, inside and outside their walls, of two different products, one being forty-three times more abundant than the other; thus, the contact surface, in comparison to the volume, is greatly increased. The induction of the luminous reaction by change in the permeability of the microtubule walls, allowing contact between the two substances, is suggested as a working hypothesis. There is an evolution of the grains along the axis of the photocytes. The grains are often surrounded by progressively increasing amounts of glycogen. Their paracrystalline disposition is altered at the apex of the luminous cells.

Fine structure of zoosporulation in Perkinsus atlanticus (Apicomplexa: Perkinsea)

Parasitology ◽  
1990 ◽  
Vol 100 (3) ◽  
pp. 351-358 ◽  
Author(s):  
C. Azevedo ◽  
L. Corral ◽  
R. Cachola
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Fine Structure ◽  
Incubation Period ◽  
Developmental Stages ◽  
The Other ◽  
Polar Ring ◽  
Transmission Electron ◽  
Apical Complex

SUMMARYLight and transmission electron microscopy were used to study different stages of Perkinsus atlanticus (Apicomplexa) during induced zoosporulation, with fluid thioglycollate medium and seawater. Cytokinesis and nucleokinesis of different developmental stages were studied every 12 h during the incubation period of 72 h, at which time the zoospores became free. Uninucleated and flagellated zoospores present the apical complex formed by conoid, polar ring, micronemes, rhoptries and subpellicular microtubules observed at different sections. Ultrastructural details were compared with the other two species of the genus Perkinsus.

Comparative morphology and fine structure of a group of Umbilicaria lichens

1984 ◽  
Vol 62 (9) ◽  
pp. 1947-1964 ◽  
Author(s):  
Martha G. Scott ◽  
Douglas W. Larson
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Fine Structure ◽  
Gas Exchange ◽  
Comparative Morphology ◽  
The Other ◽  
Bright Field ◽  
Structure And Morphology ◽  
Transmission Electron ◽  
Large Numbers

The gross morphology and fine structure of tissue layers in five Umbilicaria species (U. vellea, U. mammulata, U. papulosa, U. muhlenbergii, and U. deusta) were examined using bright-field and transmission electron microscopy. Differences in the surface topography of the upper and lower cortexes of the five species were found. Four of the species contained an osmiophilic banding material on the walls of the outermost file of living upper cortical hyphae. Although the fine structure of phycobiont cells was basically similar for all species, U. vellea was found to have smaller amounts of stored starch and peripheral lipid in cells of the algal zone than the other four species. Algal–fungal contacts were not haustorial, although aplanospore clusters were penetrated by wedge-shaped intrusive hyphae. Senescent algal cells accumulated large numbers of starch grains. Hyphae in the medullary zones were found to be similar for all species with the exception of U. muhlenbergii, which had an extrahyphal, gel-like matrix. Extensive, sheetlike lamellae were also present in the lower cortex of this species. It would appear that many aspects of thallus fine structure and morphology have a direct effect on gas exchange and water relations responses previously reported in the literature.

scholarly journals Fine structure of the longitudinal flagellum in Ceratium tripos, a marine dinoflagellate

1982 ◽  
Vol 58 (1) ◽  
pp. 109-123
Author(s):  
T. Maruyama
Keyword(s):  
Electron Microscopy ◽  
Fine Structure ◽  
Single Fibre ◽  
Microscopic Investigation ◽  
Packing Material ◽  
The Other ◽  
Free Medium ◽  
Left Handed ◽  
Transmission Electron ◽  
Extended Length

The fine structure of the longitudinal flagellum in Ceratium tripos, which performs not only undulations but also retractions, has been examined in both the retracted and relaxed states. Although conventional fixation always triggered retraction, the flagellum was found to remain relaxed when it was washed briefly with Ca2+-free medium prior to fixation. Previous light-microscopic investigation showed that it contained two fibres, the axoneme and the R-fibre. The present study by transmission electron microscopy has revealed that the axoneme that appeared to be a single fibre under the light microscope is a bundle of four fibres; the 9 + 2 microtubular axoneme, the packing material, the striated fibre, and the paraxial fibre. The first two are common in the longitudinal flagella of dinoflagellates, and the axoneme presumably generates the undulation. The last two are new and unique to the longitudinal flagellum of Ceratium. The R-fibre, which probably contracts to fold the flagellum during retraction, consists of fine filaments, which pursue a loosely spiral course in the contracted state, but align longitudinally in the relaxed state. Periodic striations appear only on the extended R-fibre. The R-fibre shortens to approximately one third of its extended length and pursues a left-handed helix. The packing material, which sticks to the microtubular axoneme on one side, is connected with the R-fibre on the other side at intervals of approximately 5.8 micrograms. The retraction seems to be regulated by the Ca2+ concentration in the flagellum.

Two- or three-way observations of the identical cell elements within the same sections by LM, TEM and/or SEM

1978 ◽  
Vol 36 (2) ◽  
pp. 82-83 ◽  
Author(s):  
Nakazo Watari ◽  
Yasuaki Hotta ◽  
Yoshio Mabuchi
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Fine Structure ◽  
Light Microscopy ◽  
Thin Sections ◽  
Transmission Electron ◽  
Identical Cell ◽  
Electron Microscopes ◽  
Scanning Electron

It is very useful if we can observe the identical cell elements within the same sections by light microscopy (LM), transmission electron microscopy (TEM) and/or scanning electron microscopy (SEM) sequentially, because, the cell fine structure can not be indicated by LM, while the color is; on the other hand, the cell fine structure can be very easily observed by EM, although its color properties may not. However, there is one problem in that LM requires thick sections of over 1 μm, while EM needs very thin sections of under 100 nm. Recently, we have developed a new method to observe the same cell elements within the same plastic sections using both light and transmission (conventional or high-voltage) electron microscopes.In this paper, we have developed two new observation methods for the identical cell elements within the same sections, both plastic-embedded and paraffin-embedded, using light microscopy, transmission electron microscopy and/or scanning electron microscopy (Fig. 1).

Processing of human melanoma cells for correlative TEM, LVSEM, and LM

1991 ◽  
Vol 49 ◽  
pp. 106-107
Author(s):  
Marek Malecki ◽  
J. Victor Small ◽  
James Pawley
Keyword(s):  
Electron Microscopy ◽  
Low Voltage ◽  
Fluorescent Microscopy ◽  
Blood Stream ◽  
Surface Topology ◽  
Integrin Receptors ◽  
Transmission Electron ◽  
Develop Technology ◽  
Voltage Scanning ◽  
Mechanisms Of Adhesion

The relative roles of adhesion and locomotion in malignancy have yet to be clearly established. In a tumor, subpopulations of cells may be recognized according to their capacity to invade neighbouring tissue,or to enter the blood stream and metastasize. The mechanisms of adhesion and locomotion are themselves tightly linked to the cytoskeletal apparatus and cell surface topology, including expression of integrin receptors. In our studies on melanomas with Fluorescent Microscopy (FM) and Cell Sorter(FACS), we noticed that cells in cultures derived from metastases had more numerous actin bundles, then cells from primary foci. Following this track, we attempted to develop technology allowing to compare ultrastructure of these cells using correlative Transmission Electron Microscopy(TEM) and Low Voltage Scanning Electron Microscopy(LVSEM).

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.

Ultrastructure of the soil fungus, Geomyces pannorus

1984 ◽  
Vol 42 ◽  
pp. 738-739
Author(s):  
J. A. Traquair ◽  
E. G. Kokko
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Fine Structure ◽  
Low Temperatures ◽  
Soil Fungus ◽  
Organic Soils ◽  
Anatomical Studies ◽  
Transmission Electron ◽  
Electron Microscopical ◽  
Scanning Electron

With the advent of improved dehydration techniques, scanning electron microscopy has become routine in anatomical studies of fungi. Fine structure of hyphae and spore surfaces has been illustrated for many hyphomycetes, and yet, the ultrastructure of the ubiquitous soil fungus, Geomyces pannorus (Link) Sigler & Carmichael has been neglected. This presentation shows that scanning and transmission electron microscopical data must be correlated in resolving septal structure and conidial release in G. pannorus.Although it is reported to be cellulolytic but not keratinolytic, G. pannorus is found on human skin, animals, birds, mushrooms, dung, roots, and frozen meat in addition to various organic soils. In fact, it readily adapts to growth at low temperatures.

Fine structure and possible functions of the hermaphrodite duct of some pulmonate snails (Mollusca: Gastropoda)

1990 ◽  
Vol 48 (3) ◽  
pp. 68-69
Author(s):  
Alan N. Hodgson
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Fine Structure ◽  
Seminal Vesicle ◽  
Reproductive Biology ◽  
Light Microscope ◽  
Light Microscope Level ◽  
Transmission Electron ◽  
Standard Techniques

The hermaphrodite duct of pulmonate snails connects the ovotestis to the fertilization pouch. The duct is typically divided into three zones; aproximal duct which leaves the ovotestis, the middle duct (seminal vesicle) and the distal ovotestis duct. The seminal vesicle forms the major portion of the duct and is thought to store sperm prior to copulation. In addition the duct may also play a role in sperm maturation and degredation. Although the structure of the seminal vesicle has been described for a number of snails at the light microscope level there appear to be only two descriptions of the ultrastructure of this tissue. Clearly if the role of the hermaphrodite duct in the reproductive biology of pulmonatesis to be understood, knowledge of its fine structure is required.Hermaphrodite ducts, both containing and lacking sperm, of species of the terrestrial pulmonate genera Sphincterochila, Levantina, and Helix and the marine pulmonate genus Siphonaria were prepared for transmission electron microscopy by standard techniques.

Use of electron microscopy to characterize the surfaces of flocculent and nonflocculent yeast cells

1989 ◽  
Vol 35 (12) ◽  
pp. 1081-1086 ◽  
Author(s):  
Byron F. Johnson ◽  
L. C. Sowden ◽  
Teena Walker ◽  
Bong Y. Yoo ◽  
Gode B. Calleja
Keyword(s):  
Electron Microscopy ◽  
Fission Yeast ◽  
Budding Yeast ◽  
The Other ◽  
Yeast Cells ◽  
Scanning Electron Micrographs ◽  
Soft Or ◽  
Transmission Electron ◽  
Scanning Transmission ◽  
Scanning Electron

The surfaces of flocculent and nonflocculent yeast cells have been examined by electron microscopy. Nonextractive preparative procedures for scanning electron microscopy allow comparison in which sharp or softened images of surface details (scars, etc.) are the criteria for relative abundance of flocculum material. Asexually flocculent budding-yeast cells cannot be distinguished from nonflocculent budding-yeast cells in scanning electron micrographs because the scar details of both are well resolved, being hard and sharp. On the other hand, flocculent fission-yeast cells are readily distinguished from nonflocculent cells because fission scars are mostly soft or obscured on flocculent cells, but sharp on nonflocculent cells. Sexually and asexually flocculent fission-yeast cells cannot be distinguished from one another as both are heavily clad in "mucilaginous" or "hairy" coverings. Examination of lightly extracted and heavily extracted flocculent fission-yeast cells by transmission electron microscopy provides micrographs consistent with the scanning electron micrographs.Key words: flocculation, budding yeast, fission yeast, scanning, transmission.

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