scholarly journals Petrology and mineralogy of the Viñales meteorite, the latest fall in Cuba

2021 ◽  
Vol 104 (2) ◽  
pp. 003685042110198
Author(s):  
Feng Yin ◽  
Deqiu Dai
Keyword(s):  
Microprobe Analysis ◽  
Electron Microprobe Analysis ◽  
Optical Microscope ◽  
Chemical Compositions ◽  
Atmospheric Entry ◽  
Thin Sections ◽  
Homogeneous Chemical ◽  
Del Rio ◽  
The Masses ◽  
Metal Phases

The new Cuban chondrite, Viñales, fell on February first, 2019 at Pinar del Rio, northwest of Cuba (22°37′10″N, 83°44′34″W). A total of about 50–100 kg of the meteorite were collected and the masses of individual samples are in a range 2–1100 g. Two polished thin sections were studied by optical microscope, Raman spectroscopy and electron microprobe analysis in this study. The meteorite mainly consists of olivine (Fa24.6), low-Ca pyroxene (Fs20.5), and troilite and Fe-Ni metal, with minor amounts of feldspar (Ab82.4-84.7). Three poorly metamorphosed porphyritic olivine-pyroxene and barred olivine chondrules are observed. The homogeneous chemical compositions and petrographic textures indicate that Viñales is a L6 chondrite. The Viñales has fresh black fusion crust with layered structure, indicating it experienced a high temperature of ∼1650°C during atmospheric entry. Black shock melt veins with width of 100–600 μm are pervasive in the Viñales and olivine, bronzite, and metal phases are dominate minerals of the shock melt vein. The shock features of major silicate minerals suggest a shock stage S3, partly S4, and the shock pressure could be >10 GPa.

Low Z Elemental Analysis using Energy Loss Electrons in a Scanning Microscope

1973 ◽  
Vol 31 ◽  
pp. 290-291
Author(s):  
D. E. Johnson ◽  
M. Isaacson
Keyword(s):  
Production Efficiency ◽  
Microprobe Analysis ◽  
Electron Microprobe Analysis ◽  
Solid Angle ◽  
Collection Efficiency ◽  
Fluorescence Yield ◽  
X Rays ◽  
Scanning Microscope ◽  
Thin Sections ◽  
X Ray

Electron microprobe analysis has been used increasingly in, recent years for low Z analysis of thin biological sections. Although this technique has produced useful results, the sensitivity is limited by two main factors. First, the fluorescence yield (wK) decreases rapidly with decreasing Z. Using the value of wK (for carbon for example, only about one out of every 400 K ionizations in carbon results in a carbon x-ray. Second, this poor x-ray production efficiency is coupled with the inherently poor x-ray collection efficiency of most microprobe detectors. In thin sections the x-rays are emitted uniformly over 4TT steradians but the detector subtends only a small solid angle at the specimen. Hall estimates the collection efficiency of most diffracting detectors at 10−4 and, with the qualification of much lower peak to background ratios, he estimates the collection efficiency of solid state nondiffractive detectors as 10−4 to 10−2.

Scanning Electron Microscopy and Electron Microprobe Analysis of Malignant Cell Cultures

1968 ◽  
Vol 26 ◽  
pp. 164-165
Author(s):  
R. I. Johnsson-Hegyeli ◽  
A. F. Hegyeli ◽  
D. K. Landstrom ◽  
W. C. Lane
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Cell Cultures ◽  
Electron Microprobe ◽  
Microprobe Analysis ◽  
Electron Microprobe Analysis ◽  
Three Dimensional ◽  
Malignant Cell ◽  
Interference Microscopy ◽  
Scanning Electron

Last year we reported on the use of reflected light interference microscopy (RLIM) for the direct color photography of the surfaces of living normal and malignant cell cultures without the use of replicas, fixatives, or stains. The surface topography of living cells was found to follow underlying cellular structures such as nuceloli, nuclear membranes, and cytoplasmic organelles, making possible the study of their three-dimensional relationships in time. The technique makes possible the direct examination of cells grown on opaque as well as transparent surfaces. The successful in situ electron microprobe analysis of the elemental composition and distribution within single tissue culture cells was also reported.This paper deals with the parallel and combined use of scanning electron microscopy (SEM) and the two previous techniques in a study of living and fixed cancer cells. All three studies can be carried out consecutively on the same experimental specimens without disturbing the cells or their structural relationships to each other and the surface on which they are grown. KB carcinoma cells were grown on glass coverslips in closed Leighto tubes as previously described. The cultures were photographed alive by means of RLIM, then fixed with a fixative modified from Sabatini, et al (1963).

Some early history of replica techniques for electron microscopy

1992 ◽  
Vol 50 (2) ◽  
pp. 1076-1077
Author(s):  
Robert M. Fisher
Keyword(s):  
Thin Film ◽  
Electron Microscopy ◽  
Optical Microscope ◽  
Early History ◽  
Bulk Materials ◽  
Thin Sections ◽  
Transmission Electron ◽  
Reflected Light ◽  
History Of ◽  
Electron Microscopes

By 1940, a half dozen or so commercial or home-built transmission electron microscopes were in use for studies of the ultrastructure of matter. These operated at 30-60 kV and most pioneering microscopists were preoccupied with their search for electron transparent substrates to support dispersions of particulates or bacteria for TEM examination and did not contemplate studies of bulk materials. Metallurgist H. Mahl and other physical scientists, accustomed to examining etched, deformed or machined specimens by reflected light in the optical microscope, were also highly motivated to capitalize on the superior resolution of the electron microscope. Mahl originated several methods of preparing thin oxide or lacquer impressions of surfaces that were transparent in his 50 kV TEM. The utility of replication was recognized immediately and many variations on the theme, including two-step negative-positive replicas, soon appeared. Intense development of replica techniques slowed after 1955 but important advances still occur. The availability of 100 kV instruments, advent of thin film methods for metals and ceramics and microtoming of thin sections for biological specimens largely eliminated any need to resort to replicas.

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