USGS · 70036674
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H.A. Lowers. 2009-07-26. A multifaceted approach to particle analysis. https://doi.org/10.1017/s1431927609099188
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Angrite meteorites represent interesting sampling of planetary crustal environments. Quench-textured angrites with strong crystal zoning originated from the shallow surface region, with evidence of reducing conditions during solidification. Plutonic angrites have more coarse-grained igneous and metamorphic textures with comparatively less zoning and are interpreted as having equilibrated at greater depth. Plutonic angrites contain the minerals magnetite Fe 3 O 4 comprised of Fe 2+ and Fe 3+ , and rhönite, where Fe 3+ is required by inspection of mineral stoichiometry. NWA 15507 is a plutonic angrite with a microgabbroic texture (mean grainsize ∼1.4 mm) composed of zoned Al-Ti-augite, Ca-bearing olivine, anorthite, with accessory kirschsteinite, rhönite, hercynite, low-Ni kamacite, merrillite, Ti-free magnetite and troilite [ 1 ]. Rhönite analyzed by electron-probe microanalysis (EPMA) has the formula Ca 2.04 (Mg 0.32 Fe 2+ 4.25 Fe 3+ 0.47 Ti 0.33 Al 0.61 )(Si 3.74 Al 2.26 )O 20 , where Fe 3+ was estimated by stoichiometric analysis. During preliminary cathodoluminescence (CL) analysis, complex subgrain and oscillatory zoning was observed in the anorthite. In this study we use a combined approach of electron probe microanalysis (EPMA), cathodoluminescence (CL), electron-backscatter diffraction (EBSD), and laser ablation inductively-coupled plasma mass spectrometry (LA-ICP-MS) to further investigate the anorthite and distribution of Fe 3+ in NWA 15507.
Cultures throughout history have valued jadeite jade (hereinafter jade), a natural material assemblage composed predominately of the NaAl endmember pyroxene, jadeite (NaAlSi 2 O 6 ) that is prized for its mechanical properties and enticing coloration [ 1 , 2 ]. The geological setting for the formation of jadeite-rich rocks and associated complex geochemical phenomena is well documented in the literature [ 3-5 ]. Unlike single crystal gems, jade often contains a mixture of colors, but the stone is perhaps best known for exhibiting a range of green hues from pale green to blue green, and to deep green [ 1 , 6 ]. Efforts to classify jade color include qualitative matching to a set of reference color tiles, and less commonly, use of a more quantitative set of color perception values first established by International Commission on Illumination’s (CIE 1931) color space, which includes values for light-dark luminance level (L*), a green-red vector (a*), and a blue-yellow vector (b*) [ 7 , 8 ]. Two principal mechanisms have been identified as the cause of green coloration in jadeite: 1) the chemical state of impurity Fe, either 2+ or 3+, and 2) minor to trace Cr in the crystal structure [ 9 , 10 ]. Previous studies have associated Cr 3+ with cathodoluminescence (CL) spectral features in jadeite using point spectrometry, with more recent connections made via 2D CL spectrum imaging [ 11-13 ]. In this effort, we are seeking to establish whether Cr impurities are correlated with green coloration in jadeite using micro-scale (≤110 μm) visible-near infrared (VIS-NIR) reflectance spectrometry.
Options for selecting a high Na concentration mineral for instrument calibration that are suitably stable under the electron beam are limited [ 1 ]. NaCl (approximately a mass fraction of 39 % Na) is not practical for use alongside other embedded and polished materials in a mounted block of standards. While albite (NaAlSi 3 O 8 ; approximately a mass fraction of 8 % Na) represents a typical choice for some microanalysts, it may be subject to time dependent signal intensity issues, such as those observed for Na and other cations during analysis of hydrous glasses [ 2 ]. Near endmember jadeite pyroxene (NaAlSi 2 O 6 ; approximately mass fraction of 11 % Na) represents a desirable option for calibration given its relatively large concentration of Na and insensitivity to electron beam radiation with respect to X-ray output. Despite these desirable characteristics, jadeites have been shown to contain complex microstructures as the result of intracrystalline zoning [ 3 , 4 ], and the impact of chemical inhomogeneity within mineral standards and natural glasses has been documented [ 5-7 ]. In this study, a commercially obtained jadeite crystal (source location “China”) was studied to assess its microscale uniformity using a suite of microbeam methods, including dispersive red-green-blue multispectral cathodoluminescence imaging (CL RGB ), hyperspectral CL imaging spectrometry, energy dispersive X-ray spectrometry (EDS), SEM-based micro-X-ray fluorescence (μXRF), and wavelength dispersive X-ray spectrometry (WDS).