scholarly journals Use of Epifluorescence Microscopy and Transmission Electron Microscopy to Investigate Spatial and Temporal Dynamics of Prokaryotes, Viruses, and Viral Infections of Prokaryotes in Mono Lake, California

2005 ◽  
Vol 11 (S02) ◽  
Author(s):  
J R Brum ◽  
G F Steward ◽  
S C Jiang ◽  
R Jellison
2005 ◽  
Vol 13 (5) ◽  
pp. 22-25
Author(s):  
Januario C. Estrada ◽  
M. Angelica Selim ◽  
Sara E. Miller

Viral infections can be focal and therefore difficult to find by electron microscopy. In addition to sampling limitations, sometimes the only specimen available for examination is tissue that has already been prepared for light microscopy (LM). We have diagnosed a papovavirus infection in skin by embedding hematoxylin and eosin (H&E)-stained sections for ultrathin sectioning and transmission electron microscopy (TEM).Immunosuppressed patients can have unusual infections or infections in unusual locations. These agents may be difficult to identify due to their not being suspected and incorrect tests being ordered.


2001 ◽  
Vol 79 (4) ◽  
pp. 726-736 ◽  
Author(s):  
Klaus W Wolf ◽  
Walton Reid

Egg morphology and hatching in the stink bug Mormidea pictiventris (Hemiptera: Pentatomidae) are described with the aid of scanning electron microscopy. In addition, the eggshell is analyzed using transmission electron microscopy and the distribution of follicle cells at the surface of ovarian eggs is studied by epifluorescence microscopy using a DNA-specific fluorescent dye. The surface of the barrel-shaped eggs carries numerous slender processes. Binucleate follicle cells, in most cases arranged in a hexagonal pattern, are responsible for the synthesis of this portion of the eggshell. The rim at the anterior pole of the egg is studded at irregular intervals with short columnar processes, the aero-micropylar processes. Hatching occurs at this pole. The prolarva is wrapped in an embryonic cuticle. Its head portion carries a Y-shaped element, the egg-burster. The major features of the inner face of the eggshell are subtle, radially oriented grooves at the anterior plate and a hexagonal pattern to the surface ornamentation throughout the remainder of the eggshell. Transmission electron microscopy revealed that the processes extending from the surface of the eggshell have a coarse texture, while the eggshell proper is composed of amorphous material. The innermost layer, however, has a trabecular organization. The findings in M. pictiventris are compared with morphological observations on the eggshell in other families of Hemiptera and suggestions are made concerning the meaning of the diverse structures.


1989 ◽  
Vol 67 (4) ◽  
pp. 1024-1031
Author(s):  
R. J. McGovern ◽  
R. K. Horst ◽  
H. W. Israel

In epifluorescence diagnostic procedures for chrysanthemum phloem necrosis, autofluorescence, aniline blue, and various nucleic acid "specific" fluorochromes such as 33258-Hoechst, 4′,6-diamidino-2-phenyl-indole-dichloride, berberine sulfate, ethidium bromide, and acridine orange were utilized. Increased fluorescence in foliar phloem correlated precisely with gross symptoms of chrysanthemum phloem necrosis by all techniques and was used, in the case of berberine sulfate, to facilitate detection of mycoplasmalike organisms by transmission electron microscopy.


Author(s):  
G. G. Shaw

The morphology and composition of the fiber-matrix interface can best be studied by transmission electron microscopy and electron diffraction. For some composites satisfactory samples can be prepared by electropolishing. For others such as aluminum alloy-boron composites ion erosion is necessary.When one wishes to examine a specimen with the electron beam perpendicular to the fiber, preparation is as follows: A 1/8 in. disk is cut from the sample with a cylindrical tool by spark machining. Thin slices, 5 mils thick, containing one row of fibers, are then, spark-machined from the disk. After spark machining, the slice is carefully polished with diamond paste until the row of fibers is exposed on each side, as shown in Figure 1.In the case where examination is desired with the electron beam parallel to the fiber, preparation is as follows: Experimental composites are usually 50 mils or less in thickness so an auxiliary holder is necessary during ion milling and for easy transfer to the electron microscope. This holder is pure aluminum sheet, 3 mils thick.


Author(s):  
R. W. Anderson ◽  
D. L. Senecal

A problem was presented to observe the packing densities of deposits of sub-micron corrosion product particles. The deposits were 5-100 mils thick and had formed on the inside surfaces of 3/8 inch diameter Zircaloy-2 heat exchanger tubes. The particles were iron oxides deposited from flowing water and consequently were only weakly bonded. Particular care was required during handling to preserve the original formations of the deposits. The specimen preparation method described below allowed direct observation of cross sections of the deposit layers by transmission electron microscopy.The specimens were short sections of the tubes (about 3 inches long) that were carefully cut from the systems. The insides of the tube sections were first coated with a thin layer of a fluid epoxy resin by dipping. This coating served to impregnate the deposit layer as well as to protect the layer if subsequent handling were required.


Author(s):  
S. Fujishiro

The mechanical properties of three titanium alloys (Ti-7Mo-3Al, Ti-7Mo- 3Cu and Ti-7Mo-3Ta) were evaluated as function of: 1) Solutionizing in the beta field and aging, 2) Thermal Mechanical Processing in the beta field and aging, 3) Solutionizing in the alpha + beta field and aging. The samples were isothermally aged in the temperature range 300° to 700*C for 4 to 24 hours, followed by a water quench. Transmission electron microscopy and X-ray method were used to identify the phase formed. All three alloys solutionized at 1050°C (beta field) transformed to martensitic alpha (alpha prime) upon being water quenched. Despite this heavily strained alpha prime, which is characterized by microtwins the tensile strength of the as-quenched alloys is relatively low and the elongation is as high as 30%.


Author(s):  
Nakazo Watari ◽  
Yasuaki Hotta ◽  
Yoshio Mabuchi

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).


Sign in / Sign up

Export Citation Format

Share Document