Christian de Capitani

The computation of equilibrium assemblage diagrams with Theriak/Domino software

Abstract In this paper, the term “equilibrium assemblage diagrams” refers to diagrams strictly based on assemblages predicted by Gibbs free energy minimization. The presented Theriak/Domino software uses a unique algorithm of scanning and bookkeeping, which allows to compute completely and automatically a great variety of diagrams: phase diagrams, pseudo-binary, pseudo-ternary, isopleths, modal amounts, molar properties of single phases or bulk-rock properties like total ΔG, volume of solids, etc. The speed and easiness of use makes thermodynamic modeling accessible to any student of Earth sciences and offers a powerful tool to check the consistency of thermodynamic databases, develop new solution models, plan experimental work, and to understand natural systems. The examples described in this paper demonstrate the capacity of the software, but also to show the usefulness and limitations of computed equilibrium assemblage diagrams. For most illustrations, a metapelite (TN205) from the eastern Lepontine Alps is used. The applications include the interpretation of complex diagrams, mineral reactions, the effect of Al content on the equilibrium assemblages, the interpretation of Si per formula unit in white mica, understanding some features of garnet growth, dehydration and isothermal compressibility, a broadening of the concept of AFM diagrams, combining equilibrium assemblage diagram information with thermobarometry, and comparing the results produced with different databases. Equilibrium assemblage diagrams do not always provide straightforward answers, but mostly stimulate further thought

Blueschists, eclogites, and decompression assemblages of the Zermatt-Saas ophiolite: High-pressure metamorphism of subducted Tethys lithosphere

Abstract The Zermatt-Saas ophiolite of the Swiss Alps represents a complete sequence of Mesozoic Tethys oceanic lithosphere. The ophiolite was subducted during early phases of the Alpine orogeny and the mafic rocks were transformed to eclogites and blueschists. Metabasalts locally preserve pillow structures in which glaucophanite forms rims on eclogitic pillow cores. Omphacite-garnet-glaucophane-epidote-ferroan dolomite-Mg-chloritoid-talc-paragonite-chlorite. rutile form characteristic coeval blueschist- and eclogite-facies assemblages. Omphacite + garnet + glaucophane + epidote + rutile represents an equilibrium assemblage that formed during deformation and in the period when the rocks reached the greatest depth of subduction. In rocks containing this assemblage, an additional significant mineral pair is Mg-chloritoid + talc. Coarse chloritoid (XMg ~ 0.45) and talc formed in dispersed clusters after the last penetrative deformation. The assemblage may require > 2.7 GPa pressure to form. It developed at maximum pressure conditions corresponding to the return-point of the ophiolite in the subduction zone. Coarse paragonite and chlorite replaced parts of the earlier formed assemblages and removed free H2O from the rocks. Exhumation of the HP to UHP ophiolite rocks was accompanied by development of symplectite rims and other replacement products along grain boundaries of the eclogite minerals by decompression reactions in a fluid-deficient regime. Particularly noteworthy is the formation of margarite, paragonite, chlorite, albite, barroisite, and preiswerkite. The latter mineral, a very rare Na-biotite, formed as a result of the decomposition of chloritoid + paragonite and is associated with magnetite and hercynite. Omphacite breakdown produced diopside-albite-barroisite symplectites. Calculated equilibrium assemblage phase diagrams for metabasite compositions indicate P-T conditions of ~2.5.3.0 GPa and ~550.600 °C. The conditions of the subduction-related metamorphism denote P and T at the return-point, which coincide with the upper P-T limit of antigorite. Antigoriteserpentinites constitute the largest volume of rocks within the ophiolite. We suggest that the P-T conditions recorded by the exhumed mafic rocks are coupled to those of antigorite breakdown in the serpentinite that released large amounts of dehydration water in the subducted serpentinite slab facilitating exhumation of the Zermatt-Saas eclogites and blueschists.

Natural Mineral Particles Are Cytotoxic to Rainbow Trout Gill Epithelial Cells In Vitro

Worldwide increases in fluvial fine sediment are a threat to aquatic animal health. Fluvial fine sediment is always a mixture of particles whose mineralogical composition differs depending on the sediment source and catchment area geology. Nonetheless, whether particle impact in aquatic organisms differs between mineral species remains to be investigated. This study applied an in vitro approach to evaluate cytotoxicity and uptake of four common fluvial mineral particles (quartz, feldspar, mica, and kaolin; concentrations: 10, 50, 250 mg L−1) in the rainbow trout epithelial gill cell line RTgill-W1. Cells were exposed for 24, 48, 72, and 96 h. Cytotoxicity assays for cell membrane integrity (propidium iodide assay), oxidative stress (H2DCF-DA assay), and metabolic activity (MTT assay) were applied. These assays were complemented with cell counts and transmission electron microscopy. Regardless of mineral species, particles ≤2 µm in diameter were taken up by the cells, suggesting that particles of all mineral species came into contact and interacted with the cells. Not all particles, however, caused strong cytotoxicity: Among all assays the tectosilicates quartz and feldspar caused sporadic maximum changes of 0.8–1.2-fold compared to controls. In contrast, cytotoxicity of the clay particles was distinctly stronger and even differed between the two particle types: mica induced concentration-dependent increases in free radicals, with consistent 1.6–1.8-fold-changes at the 250 mg L−1 concentration, and a dilated endoplasmic reticulum. Kaolin caused concentration-dependent increases in cell membrane damage, with consistent 1.3–1.6-fold increases at the 250 mg L−1 concentration. All effects occurred in the presence or absence of 10% fetal bovine serum. Cell numbers per se were marginally affected. Results indicate that (i.) natural mineral particles can be cytotoxic to gill epithelial cells, (ii.) their cytotoxic potential differs between mineral species, with clay particles being more cytotoxic, and (iii.) some clays might induce effects comparable to engineered nanoparticles.