83 research outputs found

    High spectral and spatial resolution X-ray transmission radiography and tomography using a Color X-ray Camera

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    High resolution X-ray radiography and computed tomography are excellent techniques for non-destructive characterization of an object under investigation at a spatial resolution in the micrometer range. However, as the image contrast depends on both chemical composition and material density, no chemical information is obtained from this data. Furthermore, lab-based measurements are affected by the polychromatic X-ray beam, which results in beam hardening effects. New types of X-ray detectors which provide spectral information on the measured X-ray beam can help to overcome these limitations. In this paper, an energy dispersive CCD detector with high spectral resolution is characterized for use in high resolution radiography and tomography, where a focus is put on the experimental conditions and requirements of both measurement techniques

    Structurally-controlled hydrothermal alteration in the syntectonic Neoproterozoic Upper Ruvubu Alkaline Plutonic Complex (Burundi): Implications for REE and HFSE mobilities

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    International audienceThe Neoproterozoic Upper Ruvubu Alkaline Plutonic Complex (URAPC), Burundi, is located along the western branch of the East African Rift. It comprises oversaturated and undersaturated syenites and a shallow level carbonatite body (the Matongo carbonatite) that does not outcrop but has been sampled by drill-cores. The elliptic map contour of the URAPC points to a syntectonic emplacement. Large shear zones that were active during magmatic emplacement have accommodated a regional NE-SW shortening. Mineralization features of late-magmatic to hydrothermal origin are associated with the carbonatite, which, by itself, contains a dense network of calcitic veins. HFSE mineralization occurring as zircon and ilmenite megacrysts can be found in an area of intense and extensive K-fenitization, which lead to the transformation of the surrounding syenite into a dominant K-feldspar + biotite mineral assemblage (Inamvumvu area). Carbonatitic dykes (overprinted by a hydrothermal alteration) are present a few kilometers north of the Matongo carbonatite, within highly deformed zones in the syenite. These dykes occur along with Na-fenites (resulting from the transformation of the feldspathoidal syenite into an albite-dominant paragenesis) and are enriched in REE-minerals (monazite and ancylite-(Ce)). Many magmatic (pegmatoid) dykes and hydrothermal (quartz + hematite) veins also occur in shear zones in the URAPC. Most of them can be interpreted as tension gashes. The chondrite-normalized REE patterns of some carbonatite whole rock samples are highly disturbed, in relation to post-magmatic hydrothermal alteration. The HFSE and REE distribution in the minerals from the hydrothermal veins/dykes (calcitic veins within the carbonatite, carbonatite dykes overprinted by a hydrothermal alteration in deformed zones, and zircon and ilmenite megacrysts) attests for a complex behaviour of REE during alteration. Oxygen and carbon isotope compositions of the Matongo carbonatite and the carbonatitic dykes have a magmatic signature, with 7.2 < δ18O (vs. SMOW) < 8.5‰ and -4.7 < δ13C (vs. PDB) < -5.4‰ in agreement with the Sr isotopic composition. The oxygen isotope composition of zircon and ilmenite megacrysts (δ18OZr = 4 to 4.7‰, δ18OIlm = -4.3 to -1.5‰ respectively) also point to a magmato-hydrothermal origin of the forming fluids. Some samples of the Matongo carbonatite and the carbonatitic dykes, with high δ18O values (δ18O = 8.6 to 21.8‰), show evidence of a medium- to low-temperature hydrothermal alteration event by an aqueous fluid. Calcitic veins in the carbonatite record another alteration event, outlined by the co-variation of δ18O and δ13C values (δ18O = 16.3 to 24.7‰ and δ13C = -4.7 to 0.2‰), implying the involvement of a mixed H2O-CO2 fluid. As a whole, the circulation of fluids in the URAPC was initiated during magmatic emplacement and the geometry of this circulation was controlled by the syn-emplacement crustal scale shear zones. Element mobility, one expression of which being the mineralization features described here, follow the same scheme

    Safety and immunomodulatory properties of equine peripheral blood-derived mesenchymal stem cells in healthy cats

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    Objective: Due to the immunomodulatory properties of mesenchymal stem cells (MSCs) through stimulation of endogenous immune cells by paracrine signals and cell contact, they have been proposed as alternative treatment option for many inflammatory and immune-mediated diseases in veterinary medicine. However, the long-term cultivation possibilities of feline MSCs are currently compromised due to a restricted proliferation capacity. Therefore, the xenogeneic use of equine peripheral blood-derived MSCs (ePB-MSCs) would present an interesting alternative thanks to their superior cultivation properties. To the authors' knowledge, there are currently no safety reports concerning the xenogeneic use of ePB-MSCs in cats. Therefore, the overall goal of this preliminary study was to investigate if ePB-MSCs can safely be administered in healthy cats and by extension evaluating their immunogenic and immunomodulatory properties. Methods: Ten healthy cats were intravenously (i.v.) injected with 3 x 10(5) ePB-MSCs at three time points (T-0, T-1, T-2). All cats were daily inspected by the caretaker and underwent a physical examination with hematological and biochemical analysis at day 0 (T-0), week 2 (T-1), week 4 (T-2) and week 6 (T-3) by a veterinarian. Furthermore, a modified mixed lymphocyte reaction (MLR) was performed at T-0 and T-3 for each cat in order to evaluate immunogenic and immunomodulatory properties of the ePB-MSCs Results: No adverse clinical effects could be detected following repeated i.v. administration of ePB-MSCs in all cats. Significant lower protein (T-1: P-value = 0.002; T-2: P-value > 0.001; T-3: P-value = 0.004) and albumin levels (T-1: P-value = 0.003; T-2: P-value = 0.001) were seen after repeated administration of ePB-MSCs, compared to T-0. However, all biochemical and hematological parameters stayed within clinical acceptance level. In addition, the repeated injections did not induce a cellular immune response before and after repeated ePB-MSCs administration. Furthermore, convincing immunomodulatory properties of ePB-MSCs on feline peripheral blood mononuclear cells were confirmed in the MLR-assay Conclusion: This preliminary study demonstrates that ePB-MSCs can safely be administered in healthy cats and provide a promising alternative for the treatment of various inflammatory diseases in cats
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