SYNCHROTRON-BASED TRANSMISSION X-RAY MICROSCOPY: A TOOL FOR THREE-DIMENSIONAL SPECTROSCOPIC IMAGING AND NUMERICAL SIMULATIONS

2016 ◽  
Vol 19 (1) ◽  
pp. 127-158 ◽  
Author(s):  
Matthew B. DeGostin ◽  
Alex P. Cocco ◽  
Wilson K. S. Chiu
2010 ◽  
Vol 713 (1) ◽  
pp. L74-L78 ◽  
Author(s):  
D. Falceta-Gonçalves ◽  
A. Caproni ◽  
Z. Abraham ◽  
D. M. Teixeira ◽  
E. M. de Gouveia Dal Pino

2018 ◽  
Vol 36 (4) ◽  
pp. 1 ◽  
Author(s):  
William Godoy de Azevedo Lopes de Silva ◽  
Edmilson Helton Rios ◽  
Fernanda Oliveira Hoerlle ◽  
Elizabeth May Braga Dulley Pontedeiro ◽  
Leonardo Fonseca Borghi de Almeida ◽  
...  

ABSTRACT. Characterization of carbonate rocks presents several challenges regarding the acquisition of petrophysical parameters and the understanding of fluid-flow dynamics in their pore system. To face these challenges, techniques such as X-ray microtomography, three-dimensional digital model reconstruction and fluid-flow numerical simulations have been continuously developed and improved. This study analyzes the representative elementary volume (REV) of a region of interest (ROI) of a highly heterogeneous stromatolite sample. Porosity and permeability are estimated for different subvolumes of the sample based on digital petrophysics. All necessary steps for reconstruction and segmentation of the complex pore system of the sample, as well as numerical simulations of fluid flow, are presented and discussed. The workflow is promising for reservoir evaluation because it can be applied to any type of carbonate rock.Keywords: Stromatolite, mCT, segmentation, REV, digital petrophysicsRESUMO. A caracterização de rochas carbonáticas apresenta diversos desafios quanto à determinação de seus parâmetros petrofísicos e o entendimento da dinâmica de escoamento de fluidos em seus sistemas porosos. Técnicas como a microtomografia de raios X, a modelagem digital tridimensional e a simulação numérica do escoamento de fluidos têm sido continuamente desenvolvidas e aprimoradas para superar esses desafios. Este estudo analisa o volume elementar representativo (REV) em uma região de interesse (ROI) de uma amostra de estromatólito altamente heterogênea. A porosidade e a permeabilidade são estimadas em diferentes subvolumes da amostra através da petrofísica digital. São apresentadas e discutidas todas as etapas necessárias para a reconstrução e segmentação do sistema poroso e a simulação numérica do escoamento de fluidos. A metodologia é promissora para avalição de reservatórios visto que o fluxo de trabalho pode ser aplicado a qualquer tipo de rocha carbonática.Palavras-chave: Estromatólitos, mCT, segmentação, REV, petrofísica digital


Author(s):  
James A. Lake

The understanding of ribosome structure has advanced considerably in the last several years. Biochemists have characterized the constituent proteins and rRNA's of ribosomes. Complete sequences have been determined for some ribosomal proteins and specific antibodies have been prepared against all E. coli small subunit proteins. In addition, a number of naturally occuring systems of three dimensional ribosome crystals which are suitable for structural studies have been observed in eukaryotes. Although the crystals are, in general, too small for X-ray diffraction, their size is ideal for electron microscopy.


Author(s):  
S. Cusack ◽  
J.-C. Jésior

Three-dimensional reconstruction techniques using electron microscopy have been principally developed for application to 2-D arrays (i.e. monolayers) of biological molecules and symmetrical single particles (e.g. helical viruses). However many biological molecules that crystallise form multilayered microcrystals which are unsuitable for study by either the standard methods of 3-D reconstruction or, because of their size, by X-ray crystallography. The grid sectioning technique enables a number of different projections of such microcrystals to be obtained in well defined directions (e.g. parallel to crystal axes) and poses the problem of how best these projections can be used to reconstruct the packing and shape of the molecules forming the microcrystal.Given sufficient projections there may be enough information to do a crystallographic reconstruction in Fourier space. We however have considered the situation where only a limited number of projections are available, as for example in the case of catalase platelets where three orthogonal and two diagonal projections have been obtained (Fig. 1).


Author(s):  
H.W. Deckman ◽  
B.F. Flannery ◽  
J.H. Dunsmuir ◽  
K.D' Amico

We have developed a new X-ray microscope which produces complete three dimensional images of samples. The microscope operates by performing X-ray tomography with unprecedented resolution. Tomography is a non-invasive imaging technique that creates maps of the internal structure of samples from measurement of the attenuation of penetrating radiation. As conventionally practiced in medical Computed Tomography (CT), radiologists produce maps of bone and tissue structure in several planar sections that reveal features with 1mm resolution and 1% contrast. Microtomography extends the capability of CT in several ways. First, the resolution which approaches one micron, is one thousand times higher than that of the medical CT. Second, our approach acquires and analyses the data in a panoramic imaging format that directly produces three-dimensional maps in a series of contiguous stacked planes. Typical maps available today consist of three hundred planar sections each containing 512x512 pixels. Finally, and perhaps of most import scientifically, microtomography using a synchrotron X-ray source, allows us to generate maps of individual element.


Author(s):  
Sterling P. Newberry

The beautiful three dimensional representation of small object surfaces by the SEM leads one to search for ways to open up the sample and look inside. Could this be the answer to a better microscopy for gross biological 3-D structure? We know from X-Ray microscope images that Freeze Drying and Critical Point Drying give promise of adequately preserving gross structure. Can we slice such preparations open for SEM inspection? In general these preparations crush more readily than they slice. Russell and Dagihlian got around the problem by “deembedding” a section before imaging. This some what defeats the advantages of direct dry preparation, thus we are reluctant to accept it as the final solution to our problem. Alternatively, consider fig 1 wherein a freeze dried onion root has a window cut in its surface by a micromanipulator during observation in the SEM.


Author(s):  
Daniel Beniac ◽  
George Harauz

The structures of E. coli ribosomes have been extensively probed by electron microscopy of negatively stained and frozen hydrated preparations. Coupled with quantitative image analysis and three dimensional reconstruction, such approaches are worthwhile in defining size, shape, and quaternary organisation. The important question of how the nucleic acid and protein components are arranged with respect to each other remains difficult to answer, however. A microscopical technique that has been proposed to answer this query is electron spectroscopic imaging (ESI), in which scattered electrons with energy losses characteristic of inner shell ionisations are used to form specific elemental maps. Here, we report the use of image sorting and averaging techniques to determine the extent to which a phosphorus map of isolated ribosomal subunits can define the ribosomal RNA (rRNA) distribution within them.


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