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1.
J Vis Exp ; (152)2019 10 25.
Artículo en Inglés | MEDLINE | ID: mdl-31710022

RESUMEN

Element diffusion rates and temperature/pressure control a range of fundamental volcanic and metamorphic processes. Such processes are often recorded in lamellae exsolved from host mineral phases. Thus, the analysis of the orientation, size, morphology, composition and spacing of exsolution lamellae is an area of active research in the geosciences. The conventional study of these lamellae has been conducted by scanning electron microscopy (SEM) and transmission electron microscopy (TEM), and more recently with focused ion beam (FIB)-based nanotomography, yet with limited chemical information. Here, we explore the use of atom probe tomography (APT) for the nanoscale analysis of ilmenite exsolution lamellae in igneous titanomagnetite from ash deposits erupted from the active Soufrière Hills Volcano (Montserrat, British West Indies). APT allows the precise calculation of interlamellar spacings (14-29 ± 2 nm) and reveals smooth diffusion profiles with no sharp phase boundaries during the exchange of Fe and Ti/O between the exsolved lamellae and the host crystal. Our results suggest that this novel approach permits nanoscale measurements of lamellae composition and interlamellar spacing that may provide a means to estimate the lava dome temperatures necessary to model extrusion rates and lava dome failure, both of which play a key role in volcanic hazard mitigation efforts.


Asunto(s)
Minerales/química , Tomografía Computarizada por Rayos X/métodos , Erupciones Volcánicas , Microscopía Electrónica de Rastreo , Microscopía Electrónica de Transmisión , Indias Occidentales
2.
Micron ; 80: 83-9, 2016 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-26519815

RESUMEN

Atom probe tomography (APT) combines the highest spatial resolution with chemical data at atomic scale for the analysis of materials. For geological specimens, the process of field evaporation and molecular ion formation and interpretation is not yet entirely understood. The objective of this study is to determine the best conditions for the preparation and analysis by APT of carbonate minerals, of great importance in the interpretation of geological processes, focusing on the bulk chemical composition. Results show that the complexity of the mass spectrum is different for calcite and dolomite and relates to dissimilarities in crystalochemical parameters. In addition, APT bulk chemistry of calcite closely matches the expected stoichiometry but fails to provide accurate atomic percentages for elements in dolomite under the experimental conditions evaluated in this work. For both calcite and dolomite, APT underestimates the amount of oxygen based on their chemical formula, whereas it is able to detect small percentages of elemental substitutions in crystal lattices. Overall, our results demonstrate that APT of carbonate minerals is possible, but further optimization of the experimental parameters are required to improve the use of atom probe tomography for the correct interpretation of mineral geochemistry.

3.
An Acad Bras Cienc ; 78(2): 309-15, 2006 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-16710568

RESUMEN

This work presents a geochemical study of a set of garnets, selected by their colors, from the Camafuca-Camazambo kimberlite, located on northeast Angola. Mantle-derived garnets were classified according to the scheme proposed by Grütter et al. (2004) and belong to the G1, G4, G9 and G10 groups. Both sub-calcic (G10) and Ca-saturated (G9) garnets, typical, respectively, of harzburgites and lherzolites, were identified. The solubility limit of knorringite molecule in G10D garnets suggests they have crystallized at a minimum pressure of about 40 to 45 kbar (4-4.5 GPa). The occurrence of diamond stability field garnets (G10D) is a clear indicator of the potential of this kimberlite for diamond. The chemistry of the garnets suggests that the source for the kimberlite was a lherzolite that has suffered a partial melting that formed basaltic magma, leaving a harzburgite as a residue.

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