Deformed rocks of the Itabira Iron Formation (itabirites) in Brazil show microstructural evidence of pressure solution of quartz and iron oxides; it appears that magnetite was dissolved and hematite precipitated. The dissolution of magnetite seems to be related to its transformation to hematite by oxidation of Fe2+ to Fe3+. The transformation of magnetite to hematite occurs along {111} planes, and results in the development of hematite domains along {111} that are parallel to the foliation. The difference in volume created by the transformation of magnetite to hematite and the shear stress acting on the interphase boundaries allow fluids to migrate along these planes. The dissolution of magnetite involves the hydrolyzation of the Fe2+MO bonds at interphase boundaries of high normal stress. The high fugacity of oxygen in the fluid phase promotes the reaction of Fe2+ (in solution) with oxygen. Fe2+ ions oxidize to Fe3+ and precipitate as hematite platelets with their longest axes oriented parallel to the direction of maximum stretching. The transformation of magnetite to hematite during deformation plays an important role in the fabric evolution of the iron formation rocks. The transformation along {111} creates planes of weakness that facilitate fracturing. The fracturing plus the dissolution result in a reduction of magnetite grain size, and the oriented precipitation results in layers of hematite platelets. These processes produce a new fabric characterized by a penetrative foliation and lineation.

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A study of the cathodoluminescence (CL) properties of imperial topaz from Ouro Preto region (Minas Gerais state, Brazil) and its relation with trace-element composition was conducted, using scanning electron microscope cathodoluminescence (SEM-CL), optical microscope cathodoluminescence (OM-CL), cathodoluminescence-spectrometry (CL-spectrometry), electron microprobe analysis (EMPA), laser ablation inductively-coupled plasma mass spectrometry (LA-ICP-MS) and Raman spectrometry. Each analytical technique allowed characterization of the imperial topaz fingerprint. SEM-CL panchromatic images show different crystal growth and resorption events in imperial topaz crystals. Colour CL images indicate only blue to violet emissions. The CL-spectra indicate a broad emission band with low intensity peak at ~417 nm and a broad emission band with high intensity and major peaks at 685, 698, 711 and 733 nm. The EMPA indicates high OH content, in which the OH/(OH + F) ratio ranges between 0.35–0.43 (0.72 ≤ OH ≤ 0.86 apfu). High Cu and Zn concentrations (LA-ICP-MS) were measured in the high luminescence areas of SEM-CL images, suggesting both elements as CL-activators in imperial topaz. Raman and CL-spectra indicate high Cr concentrations, corroborated by EMPA and LA-ICP-MS results. The high Cr caused strong luminescence intensities that enabled their superimposition over the OH stretching mode (~3650 cm–1) of topaz in all Raman spectra. Among trace elements, the concentrations of Ti, V, Cr, Mn, Fe, Cu, Zn, Ga and Ge provide the fingerprint of imperial topaz.

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