Abstract We have conducted geochemical and mineralogical investigations of the rare earth and yttrium ( REY )‐rich mud from the M inami‐ T orishima area in the P acific in order to clarify the concentration of REY and their host‐phase in the mud. X ‐ray diffraction analysis shows that the mud is mainly composed of phillipsite, fluorapatite, quartz, albite, illite and montmorillonite. Whole‐rock CaO , P 2 O 5 and total REY contents of the mud are positively correlated. Relative abundance of apatite is also positively correlated to P 2 O 5 and total REY contents. These correlations suggest that apatite is the main host of the P 2 O 5 and REY in the mud. We make in situ compositional analyses of constituent minerals in the REY mud . The results show that the apatite is abundant in REY (9300–32,000 ppm) and is characterized by a negative Ce anomaly and enrichment in heavy rare‐earth elements. This abundance and composition of REY of the mud is similar those of fish debris apatites. In contrast, phillipsite is less abundant in REY (60–170 ppm). Therefore we conclude that the main REY host phase of the mud is apatite.
Little is known about the nature of ore fluid at the Sopokomil shale-hosted massive sulfide Zn-Pb deposit (North Sumatra, Indonesia). We therefore investigated its ore-fluid salinities, temperatures, densities, redox state, and pH using fluid inclusion microthermometry, sphalerite composition, and thermodynamic modelling. The fluid salinities and temperatures were ≈6 wt.% NaCl equiv and ≈165 °C, respectively, corresponding to an ore fluid less dense than seawater (≈0.96 g/mL). Sphalerite contains ≈9.9 mole% FeS in the stratiform ore and ≈3.4 mole% FeS in the feeder ore, suggesting a reduced fluid, which must have been acidic to be fertile. Such redox state and acidity invoke fluid dilution as the sulfide depositional mechanism. The bulk of the sulfides were precipitated in the early stage of mixing, within T = 165–155 °C. Key ingredients of sphalerite and galena at Sopokomil include (1) Zn that was primarily transported as ZnCl+, (2) Pb that predominantly occurred as PbCl2(aq), and (3) S that was largely supplied by marine sediment porewater. This study highlights the significance of a dramatic shift in thermal and chemical equilibrium induced by fluid dilution in the making of the first significant shale-hosted massive sulfide Zn-Pb deposit in Indonesia.
Abstract Iron (Fe) oxyhydroxides (goethite and hematite) and manganese (Mn)‐oxyhydroxides (lithiophorite, asbolane, lithiophorite‐asbolane intermediate) are typically fine‐grained and poorly crystalline in nature, and as such are difficult to identify by conventional X‐ray powder diffraction. This study employs Raman spectroscopy and electron probe microanalysis (EPMA) to characterize Fe‐ and Mn‐oxyhydroxides found in the Berong Ni–Co laterite deposit at Palawan Island, Philippines. Accurate identification of these minerals is important because these phases contain high Ni and Co contents. Goethite and hematite occur in a wide range of textures, which are related to their compositional variations with respect to Ni, Al, Mn, Cr, and Si. The change in the intensity of the Raman peaks can be linked to the variable concentrations of Ni, Al, Mn, Cr, and Si in goethite. These chemical variations affect the textural transformation of goethite from amorphous to cryptocrystalline. Lithiophorite, asbolane and their intermediates were properly distinguished using Raman spectroscopy. EPMA data shows that these Mn minerals contain appreciable concentrations of Ni, Co, Al, and Fe. The band shift from lithiophorite to asbolane end terms in the 486–593 cm −1 domain indicates the substitution of Al in lithiophorite by Ni, Co, and Fe.
Abstract Mining operations in the Pinpet Fe deposit, which is the second‐largest Fe deposit in Myanmar, are currently suspended, in part because of possible contamination of heavy metals and hazardous elements (e.g., Fe, As, Cu, Zn, and U) into the surrounding aquatic environment and associated public concern. However, a scientific investigation of the source and degree of contamination in streams near the deposit has not yet been conducted. Therefore, we quantified heavy‐metal and hazardous‐element concentrations of stream waters and sediments in stream beds, and measured the speciation and concentration of these metals in deposit Fe ores using the sequential extraction method, to better understand the influence of mining activities on the surrounding environment. Geochemical results for Nan‐tank‐pauk stream and its tributaries indicate that the chemical compositions of their waters are controlled by carbonate bedrock and that no detectable contamination has occurred as a result of mining activity or hematite and limonite ore beneficiation processes in either the wet or dry seasons. All measured heavy‐metal and hazardous‐element concentrations were below the World Health Organization standards for drinking water and the proposed national drinking water quality standards in Myanmar. Bulk chemical compositions of stream‐bed and tailings dam sediments show that As, Zn, and Cu concentrations are similar to those in uncontaminated sediments. Results of bulk mineralogical and chemical analyses of ore samples reveal that some limonite ore samples contain substantial amounts of As (up to 2 wt%). However, sequential extraction results indicate that most (>90%) of the As in these As‐rich ores is hosted in insoluble fractions (e.g., crystalline Fe hydroxides and clays). Therefore, arsenic is unlikely to be released into the aquatic environment by interacting with water during ore beneficiation processes should the mine resume operations.
