The Abruzzi bauxite district includes the deposits located on the Campo Felice plateau and those of the Monti d’Ocre, which had been mined in the first part of the 20th century. Bauxite is of the karst type, with textures ranging between oolitic and oolitic-conglomeratic, the latter suggesting a partial reworking of evolved lateritic soils. The high contents of Al₂O₃ and Fe₂O₃ (average values 53.76 and 21.76 wt %, respectively) are associated with the presence of boehmite, hematite, and minor goethite. SiO₂ and TiO₂ have average values of 7.79 and 2.75 wt %, corresponding to the presence of kaolinite, anatase and rutile. Among the minor so-called “bauxitophile” elements V, Co, Ni, Cr and Zr, the most enriched is Cr, with an average value of 0.07 wt %. Nickel has an average value of 210.83 ppm. Vanadium shows an average value of 266.57 ppm, whereas the average Co concentration is 35.89 ppm. The total rare earth elements (REE) concentration in the sampled bauxite sites is variable between ca. 700 and 550 ppm. Among REEs, the most abundant element is Ce, with Ce anomalies commonly associated with authigenic REE-fluoro-carbonates, probably produced after the REEs remobilization from primary detrital minerals and their precipitation in neo-formed phases during the bauxitization process. Scandium and Ga occur in small amounts (57 and 60 ppm, respectively), but geochemical proxies of their remobilization and uptake in neo-formed minerals (Fe- and Al-(hydr)oxides, respectively) have been observed. The mean Eu/Eu* and Al₂O₃/TiO₂ ratios and the Ni-Cr contents of the Abruzzi bauxites suggest that the parent rock of these deposits was a material of acid affinity, likely corresponding to volcanic tephra or eolic loess-type sands.

Bauxites in southern France (Provence and Languedoc) have been exploited since the beginning of the last century. Though most of the deposits are now subeconomic or mined-out, these bauxites represent model analogs for other economic bauxites of the world. These Cretaceous karst-type deposits lie directly on Jurassic carbonates, and have been formed through a combination of different processes: in-situ alteration of siliciclastic sediments deposited on carbonate platforms, and reworking of early bauxites in the karst network. In this study, we present preliminary bulk rock geochemical and in-situ laser ablation (LA) -ICP-MS analyses on Al- and Fe-oxy-hydroxides of Provence (Les Baux-de-Provence) and Languedoc (Villeveyrac, Loupian) bauxites, with the aim of evaluating the concentrations of rare earth elements (REEs) and their deportment in these minerals. REEs have total average concentrations of 700 mg/kg in the analyzed samples, which are mostly composed of boehmite, γ-AlO(OH), and Fe-oxy-hydroxides (hematite and goethite). Maximum REEs concentrations are commonly associated with positive Ce anomalies in chondrite-normalized patterns. In contrast with other examples from the literature, it has been observed that high REE concentrations also occur in samples apparently devoid or poor of REE-minerals. In these samples, the total amount of REEs is positively correlated with that of Ga (commonly contained in boehmite). LA-ICP-MS trace element analyses on boehmite and Fe-oxy-hydroxides have shown that while the Al-hydroxide contains the suite of REEs, goethite and hematite are preferentially enriched only in Ce. Considering that Al-hydroxides are digested during the Bayer process, an interesting issue to develop in the future is whether (and how) REEs released during Al-hydroxide digestion could be recovered together with Al from the pregnant leach liquor, as routinely done for Ga.

Supergene nonsulfide ores form from the weathering of sulfide mineralization. Given the geochemical affinity of Ge to Si⁴⁺ and Fe³⁺, weathering of Ge-bearing sulfides could potentially lead to Ge enrichments in silicate and Fe-oxy-hydroxide minerals, although bulk rock Ge concentrations in supergene nonsulfide deposits are rarely reported. Here, we present the results of an investigation into Ge concentrations and deportment in the Cristal supergene Zn nonsulfide prospect (Bongará, northern Peru), which formed from the weathering of a preexisting Mississippi Valley-type (MVT) sulfide deposit. Material examined in this study originates from drillcore recovered from oxidized Zn-rich bodies ~ 15–20 m thick, containing ~ 5–45 wt% Zn and Ge concentrations ~ 100 ppm. Microanalysis and laser ablation-ICP-MS show that precursor sphalerite is rich in both Fe (mean Fe = 8.19 wt%) and Ge (mean Ge = 142 ppm). Using the mineral geothermometer GGIMFis—geothermometer for Ga, Ge, In, Mn, and Fe in sphalerite—proposed by Frenzel et al. (Ore Geol Rev 76:52–78, 2016 ), sphalerite trace element data from the Cristal prospect suggest a possible formation temperature (T_GGIMFis) of 225 ± 50 °C, anomalously high for a MVT deposit. Germanium concentrations measured in both goethite (mean values 100 to 229 ppm, max 511 ppm) and hemimorphite (mean values 39 to 137 ppm, max 258 ppm) are similar to concentrations measured in hypogene sphalerite. Additionally, the Ge concentrations recorded in bulk rock analyses of sphalerite-bearing and oxidized samples are also similar. A persistent warm-humid climate is interpreted for the region, resulting in the development of an oxidation zone favoring the formation of abundant Zn hydrosilicates and Fe hydroxides, both able to incorporate Ge in their crystal structure. In this scenario, Ge has been prevented from dispersion during the weathering of the Ge-bearing sulfide bodies and remains in the resultant nonsulfide ore.

Underground mining can produce subsidence phenomena, especially if orebodies are surficial or occur in soft rocks. In some countries, illegal mining is a big problem for environmental, social and economic reasons. However, when unauthorized excavation is conducted underground, it is even more dangerous because it can produce unexpected surficial collapses in areas not adequately monitored. For this reason, it is important to find quick and economic techniques able to give information about the spatial and temporal development of uncontrolled underground activities in order to improve the risk management. In this work, the differential interferometric synthetic aperture radar (DInSAR) technique, implemented in the SUBSOFT software, has been used to study terrain deformation related to illegal artisanal mining in Ecuador. The study area is located in Zaruma (southeast of El Oro province), a remarkable site for Ecuadorian cultural heritage where, at the beginning of the 2017, a local school collapsed, due to sinkhole phenomena that occurred around the historical center. The school, named “Inmaculada Fe y Alegria”, was located in an area where mining activity was forbidden. For this study, the surface deformations that occurred in the Zaruma area from 2015 to 2019 were detected by using the Sentinel-1 data derived from the Europe Space Agency of the Copernicus Program. Deformations of the order of five centimeters were revealed both in correspondence of known exploitation tunnels, but also in areas where the presence of tunnels had not been verified. In conclusion, this study allowed to detect land surface movements related to underground mining activity, confirming that the DInSAR technique can be applied for monitoring mining-related subsidence.

This work is part of a project focused on the Somma–Vesuvius volcano and aimed at identifying Cu minerals related to mineralizing processes associated with magmatic activity in an active magmatic-hydrothermal system. A mineralogical survey was carried out on a set of samples represented by sublimates and fumarolic products from the collection of the Mineralogical Museum of the University of Naples Federico II (Italy). These samples are mainly related to most recent eruptive episodes of Vesuvius activity, from 1631 onward. Copper-bearing minerals were characterized, as well as associated minerals, by X-ray diffraction (XRD) scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDS). An investigation on the structural complexity of Cu-mineral assemblages with different temperature formations was also carried out using the TOPOS software package. The main copper phases are sulfates, followed by vanadates, hydroxyhalides, oxides, carbonates, silicates and finally, phosphates. New mineral occurrences for Vesuvius, both Cu-bearing and Cu-free, are described. Nevertheless, the fumarolic/alteration minerals at Vesuvius cannot be considered of economic relevance as a copper reservoir, this type of mineralizations are significant for copper crystal chemistry and for the knowledge of the mineralogical variants. The obtained datasets can be of interest for the knowledge of volcanic byproducts of copper ore deposits (i.e., porphyry copper systems) and of (base) metal segregation processes.

The Kabwe Zn-Pb deposit (central Zambia) consists of a cluster of mixed sulfide and non-sulfide orebodies. The sulfide ores comprise sphalerite, galena, pyrite, chalcopyrite and accessory Ge-sulfides (±Ga and In). The non-sulfide ores comprise: (1) willemite-dominated zones encasing massive sulfide orebodies and (2) oxide-dominated alteration bands, overlying both the sulfide and Zn-silicate orebodies. This study focuses on the Ge, In and Ga distribution in the non-sulfide mineralization, and was carried out on a suite of Kabwe specimens, housed in the Natural History Museum Ore Collection (London). Petrography confirmed that the original sulfides were overprinted by at least two contrasting oxidation stages dominated by the formation of willemite (W1 and W2), and a further event characterized by weathering-related processes. Oxygen isotopic analyses have shown that W1 and W2 are unrelated genetically and furthermore not related to supergene Zn-Pb-carbonates in the oxide-dominated assemblage. The δ¹⁸O composition of 13.9–15.7‰ V-SMOW strongly supports a hydrothermal origin for W1. The δ¹⁸O composition of W2 (−3.5‰ to 0‰ V-SMOW) indicates that it precipitated from groundwaters of meteoric origin in either a supergene or a low-T hydrothermal environment. Gallium and Ge show a diversity of distribution among the range of Zn-bearing minerals. Gallium has been detected at the ppm level in W1, sphalerite, goethite and hematite. Germanium occurs at ppm levels in W1 and W2, and in scarcely detectable amounts in hemimorphite, goethite and hematite. Indium has low concentrations in goethite and hematite. These different deportments among the various phases are probably due to the different initial Ga, In and Ge abundances in the mineralization, to the different solubilities of the three elements at different temperatures and pH values, and finally to their variable affinities with the various minerals formed.