The Distribution of Glycogen in the Tissues of Siboglinum Atlanticum [Pogonophora]

1973 ◽  
Vol 53 (3) ◽  
pp. 665-671 ◽  
Author(s):  
Eve C. Southward
Keyword(s):  
Electron Microscopy ◽  
Light And Electron Microscopy ◽  
Epidermal Cells ◽  
Peritoneal Cells ◽  
Body Regions ◽  
Three Body

Light and electron microscopy showed the same distribution of glycogen. The peritoneal cells contain large amounts in all three body regions investigated: the forepart, metameric region and postannular region. Glycogen is present in most epidermal cells and is very abundant in some, particularly in the postannular region, but the cells which secrete the chitinous and proteinaceous components of the tube are almost devoid of glycogen.

The structure of the antennal heart of Aedes aegypti (Linnaeus)

1997 ◽  
Vol 75 (3) ◽  
pp. 444-458 ◽  
Author(s):  
B. D. Sun ◽  
J. M. Schmidt
Keyword(s):  
Electron Microscopy ◽  
Connective Tissue ◽  
Aedes Aegypti ◽  
Light And Electron Microscopy ◽  
Single Layer ◽  
Epidermal Cells ◽  
Muscle Fibres ◽  
Columnar Cells

The structure of the antennal heart of Aedes aegypti (L.) (Diptera: Culicidae) was observed using light and electron microscopy. The antennal heart consists of several distinct regions including a single layer of columnar cells, the chamber walls, the valve, the z-body, the muscle fibres, and the connective tissue filaments. The columnar cells are structurally similar to secretory and osmoregulatory cells. Features of tendinous epidermal cells typically involved in the attachment of muscles to the cuticle can be observed in various areas of the antennal heart when it is examined as a whole. A model describing the pumping mechanism of the antennal heart in A. aegypti is presented.

scholarly journals Microstructure of Soft Scald in ‘Honeycrisp’ Apples

2017 ◽  
Vol 142 (6) ◽  
pp. 464-469
Author(s):  
Yin Xu ◽  
Yizhou Ma ◽  
Nicholas P. Howard ◽  
Changbin Chen ◽  
Cindy B.S. Tong ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Cross Sections ◽  
Light And Electron Microscopy ◽  
Breeding Population ◽  
Epidermal Cells ◽  
Fruit Peel ◽  
Cellular Microstructure ◽  
Apple Cultivars ◽  
Honeycrisp Apples ◽  
Soft Scald

Soft scald is an apple (Malus ×domestica Borkh.) fruit disorder that appears in response to cold storage after about 2–8 weeks. It appears as a ribbon of dark tissue on the peel of the fruit, with occasional browning into the flesh. Several apple cultivars are susceptible to it, including Honeycrisp. The objectives of this study were to examine the cellular microstructure of fruit exhibiting soft scald and determine if any aspect of the peel microstructure at harvest could be indicative of future soft scald incidence. Light and electron microscopy were used to examine the peel microstructure of ‘Honeycrisp’ fruit that were unaffected or affected by soft scald. Tissue with soft scald had brown pigmented epidermal and hypodermal cells, whereas unaffected fruit peel epidermal cells were unpigmented. Cuticular wax of unaffected peel had upright wax platelets or clumps of wax, but peel surfaces with soft scald exhibited flattened granules and were more fragile than that of unaffected fruit. Epidermal cells of fruit with soft scald were more disorganized than that of unaffected fruit. Light microscopy was used to examine peels of ‘Honeycrisp’ fruit from four growing locations and fruit from a ‘Honeycrisp’ breeding population at harvest. ‘Honeycrisp’ and ‘Honeycrisp’ progeny fruit were also stored at 0 °C for 8 weeks and scored for soft scald incidence. Cross-sections of unaffected peel of stored ‘Honeycrisp’ fruit looked similar to that of freshly harvested fruit. No significant correlations were found between soft scald incidence and measured microstructural attributes of ‘Honeycrisp’ fruit at harvest, suggesting that peel microstructure cannot be used to predict possible soft scald incidence after storage.

Studies on Pogonophora. Fine structure of the tentacles

1966 ◽  
Vol 46 (2) ◽  
pp. 351-372 ◽  
Author(s):  
Brij L. Gupta ◽  
Colin Little ◽  
Ann M. Philip
Keyword(s):  
Electron Microscopy ◽  
Fine Structure ◽  
Surface Membrane ◽  
Light And Electron Microscopy ◽  
Epidermal Cells ◽  
Mucous Cells

The structure of the tentacle in two species of Pogonophora (of the genera Nereilinum and Oligobrachia) has been investigated by light- and electron-microscopy. The fine structure of the pinnules, epidermal cells and mucous cells is described. The surface membrane of the epidermal cells and the pinnules forms an elaborate system of microvilli which traverse the cuticle and often extend up to the surface particles.

Cytology of mucilage production in the seed coat of Candle canola (Brassica campestris)

1981 ◽  
Vol 59 (3) ◽  
pp. 292-300 ◽  
Author(s):  
L. Van Caeseele ◽  
J. T. Mills ◽  
M. Sumner ◽  
R. Gillespie
Keyword(s):  
Electron Microscopy ◽  
Seed Coat ◽  
Brassica Campestris ◽  
Light And Electron Microscopy ◽  
Epidermal Cells ◽  
Starch Grains ◽  
Golgi Bodies ◽  
Tangential Wall ◽  
Membrane Bound

The development of mucilage in the epidermal cells of canola seeds (Brassica campestris L. cv. Candle) was studied with light and electron microscopy from 5 days after pollination to maturity. During the first 17 days starch was deposited in amyloplasts. At or near the 17th day mucilage appeared between the plasmalemma and the outer tangential wall of the epidermal cells. As the volume of mucilage increased, starch grains disappeared and were totally absent by 25 days. Membrane-bound structures and Golgi bodies were visible within the cytoplasm adjacent to the site of mucilage deposition. At maturity the seed epidermal cells were totally devoid of cytoplasm and engorged with mucilage.

scholarly journals Infection Behavior of Venturia nashicola, the Cause of Scab on Asian Pears

2000 ◽  
Vol 90 (11) ◽  
pp. 1209-1216 ◽  
Author(s):  
P. Park ◽  
H. Ishii ◽  
Y. Adachi ◽  
S. Kanematsu ◽  
H. Ieki ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Cell Death ◽  
Light And Electron Microscopy ◽  
Fungal Growth ◽  
Resistance Mechanisms ◽  
Epidermal Cells ◽  
Japanese Pear ◽  
Fungal Cell ◽  
Mechanism Of Resistance ◽  
Venturia Nashicola

The infection of Japanese pear by Venturia nashicola, the cause of scab on Asian pears (Japanese pear, Pyrus pylifolia var. culta; Chinese pear, P. ussuriensis), was examined using light and electron microscopy to determine the mechanism of resistance in pears. Early stages of infection were similar on the susceptible cv. Kosui, the resistant cv. Kinchaku, and the nonhost European pear (P. communis) cv. Flemish Beauty. V. nashicola penetrated only the cuticle layer on pear leaves and formed subcuticular hyphae on all three cultivars. Hyphae were localized in the pectin layer of pear leaves and never penetrated into the cytoplasm of epidermal cells. This restriction of fungal growth suggested that pectinases released by infection hyphae or subcuticular hyphae may be important in infection. Subcuticular hyphae were modified ultrastructurally in the pectin layer of resistant pear cultivars accompanied by fungal cell death. In contrast, fungal cells appeared intact in susceptible pear cultivars, suggesting the existence of resistance mechanisms.

The Morphology of Vacuolated Cells in the Liver Following Administration of Vitamin A.

1973 ◽  
Vol 31 ◽  
pp. 408-409
Author(s):  
Odell T. Minick ◽  
Hidejiro Yokoo ◽  
Fawzia Batti
Keyword(s):  
Electron Microscopy ◽  
Body Weight ◽  
Vitamin A ◽  
Light And Electron Microscopy ◽  
Liver Cells ◽  
Prominent Feature ◽  
Vascular Space ◽  
Vacuolated Cell ◽  
Vacuolated Cells ◽  
Vacuolated Cytoplasm

Vacuolated cells in the liver of young rats were studied by light and electron microscopy following the administration of vitamin A (200 units per gram of body weight). Their characteristics were compared with similar cells found in untreated animals.In rats given vitamin A, cells with vacuolated cytoplasm were a prominent feature. These cells were found mostly in a perisinusoidal location, although some appeared to be in between liver cells (Fig. 1). Electron microscopy confirmed their location in Disse's space adjacent to the sinusoid and in recesses between liver cells. Some appeared to be bordering the lumen of the sinusoid, but careful observation usually revealed a tenuous endothelial process separating the vacuolated cell from the vascular space. In appropriate sections, fenestrations in the thin endothelial processes were noted (Fig. 2, arrow).

Control of Autogenous Vein Grafts Prior to Reimplantation, By Electron Microscopy

1972 ◽  
Vol 30 ◽  
pp. 106-107
Author(s):  
John H. L. Watson ◽  
John L. Swedo ◽  
M. Vrandecic
Keyword(s):  
Electron Microscopy ◽  
Light And Electron Microscopy ◽  
Physiological Saline ◽  
Experimental Conditions ◽  
Vein Grafts ◽  
Arterial Blood ◽  
Saphenous Veins ◽  
Autogenous Vein ◽  
Control Of Parameters ◽  
Post Implantation

The ambient temperature and the nature of the storage fluids may well have significant effects upon the post-implantation behavior of venus autografts. A first step in the investigation of such effects is reported here. Experimental conditions have been set which approximate actual operating room procedures. Saphenous veins from dogs have been used as models in the experiments. After removal from the dogs the veins were kept for two hours under four different experimental conditions, viz at either 4°C or 23°C in either physiological saline or whole canine arterial blood. At the end of the two hours they were prepared for light and electron microscopy. Since no obvious changes or damage could be seen in the veins by light microscopy, even with the advantage of tissue specific stains, it was essential that the control of parameters for successful grafts be set by electron microscopy.

Ultrastructure of two neoplasms in culture compared with original biopsies

1984 ◽  
Vol 42 ◽  
pp. 50-51
Author(s):  
Joseph M. Harb ◽  
James T. Casper ◽  
Vlcki Piaskowski
Keyword(s):  
Electron Microscopy ◽  
Tissue Culture ◽  
Biopsy Specimen ◽  
Cultured Cells ◽  
Light And Electron Microscopy ◽  
Human Tumor ◽  
Soft Agar ◽  
Human Tumor Cells ◽  
Morphological Distinction ◽  
Tumor Types

The application of tissue culture and the newer methodologies of direct cloning and colony formation of human tumor cells in soft agar hold promise as valuable modalities for a variety of diagnostic studies, which include morphological distinction between tumor types by electron microscopy (EM). We present here two cases in which cells in culture expressed distinct morphological features not apparent in the original biopsy specimen. Evaluation of the original biopsies by light and electron microscopy indicated both neoplasms to be undifferentiated sarcomas. Colonies of cells propagated in soft agar displayed features of rhabdomyoblasts in one case, and cultured cells of the second biopsy expressed features of Ewing's sarcoma.

The Effect of Vitamin A on the Intermittent Nitrogen Dioxide Gas Exposure in Hamsters

1976 ◽  
Vol 34 ◽  
pp. 176-177
Author(s):  
J.C.S. Kim ◽  
M.G. Jourden ◽  
E.S. Carlisle
Keyword(s):  
Electron Microscopy ◽  
Vitamin A ◽  
Nitrogen Dioxide ◽  
Chronic Exposure ◽  
Light And Electron Microscopy ◽  
Specific Effect ◽  
Deficient Diet ◽  
Intermittent Exposure ◽  
Hypovitaminosis A ◽  
Gas Exposure

Chronic exposure to nitrogen dioxide in rodents has shown that injury reaches a maximum after 24 hours, and a reparative adaptive phase follows (1). Damage occurring in the terminal bronchioles and proximal portions of the alveolar ducts in rats has been extensively studied by both light and electron microscopy (1).The present study was undertaken to compare the response of lung tissue to intermittent exposure to 10 ppm of nitrogen dioxide gas for 4 hours per week, while the hamsters were on a vitamin A deficient diet. Ultrastructural observations made from lung tissues obtained from non-gas exposed, hypovitaminosis A animals and gas exposed animals fed a regular commercially prepared diet have been compared to elucidate the specific effect of vitamin A on nitrogen dioxide gas exposure. The interaction occurring between vitamin A and nitrogen dioxide gas has not previously been investigated.

mRNA localization by Electron microscopic in situ hybridization

1991 ◽  
Vol 49 ◽  
pp. 430-431
Author(s):  
J. A. Pollock ◽  
M. Martone ◽  
T. Deerinck ◽  
M. H. Ellisman
Keyword(s):  
Electron Microscopy ◽  
High Resolution ◽  
Nucleic Acids ◽  
Recombinant Dna ◽  
Light And Electron Microscopy ◽  
Electron Microscopic ◽  
High Voltage Electron Microscopy ◽  
Functional Sites ◽  
Voltage Electron

Localization of specific proteins in cells by both light and electron microscopy has been facilitate by the availability of antibodies that recognize unique features of these proteins. High resolution localization studies conducted over the last 25 years have allowed biologists to study the synthesis, translocation and ultimate functional sites for many important classes of proteins. Recently, recombinant DNA techniques in molecular biology have allowed the production of specific probes for localization of nucleic acids by “in situ” hybridization. The availability of these probes potentially opens a new set of questions to experimental investigation regarding the subcellular distribution of specific DNA's and RNA's. Nucleic acids have a much lower “copy number” per cell than a typical protein, ranging from one copy to perhaps several thousand. Therefore, sensitive, high resolution techniques are required. There are several reasons why Intermediate Voltage Electron Microscopy (IVEM) and High Voltage Electron Microscopy (HVEM) are most useful for localization of nucleic acids in situ.

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