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The manganese deposits at the Kato Nevrokopi area are located in the Drama Basin (Northern Greece) and belong to the Rhodope Metamorphic Province. The deposits were previously exploited for several supergene Mn-oxide ore bodies of massive, battery-grade nsutite, spatially associated with fault zones in the vicinity of Oligocene granitic intrusions. We conducted detailed geological, mineralogical, and geochemical investigations at the Mavro Xylo deposit, which led to the identification of Ag-rich Mn-Zn±Pb vein-type mineralization. The studied paragenesis appears to have developed during two hydrothermal stages: stage I, characterized by the mineral assemblage rhodonite–quartz–rhodochrosite–pyrophanite–pyrite–galena–Te bearing argentite–sphalerite–wurtzite–alabandite, and stage II, dominated by Ag-rich, Mn-Zn±Pb oxides in the form of fracture-fills along a high-angle NE-SW fault zone in brecciated marbles. Bulk analyses of the stage-II oxide assemblage yielded concentrations of Ag up to 0.57 wt.%. In the veins, wurtzite is present in bands, succeeded by manganese oxides, while calcite and quartz are the main gangue minerals. We placed particular emphasis on the occurrence of Ag in high concentrations within distinct manganese oxides. Major silver carriers include Zn-bearing todorokite, chalcophanite, and hydrous Pb-Mn oxide. The vein-type mineralization at Mavro Xylo shares many characteristics with other intermediate-sulfidation epithermal precious metal-rich deposits associated with high Mn concentrations. The evolution of the mineral paragenesis indicates a change in the physicochemical attributes of the ore-forming fluids, from initially reducing (stage I) to oxidizing (stage II). Although the origin of the initial ore-forming fluid remains to be constrained, the above redox change is tentatively attributed to the increasing incursion of meteoric waters over time.
The manganese deposits at the Kato Nevrokopi area are located in the Drama Basin (Northern Greece) and belong to the Rhodope Metamorphic Province. The deposits were previously exploited for several supergene Mn-oxide ore bodies of massive, battery-grade nsutite, spatially associated with fault zones in the vicinity of Oligocene granitic intrusions. We conducted detailed geological, mineralogical, and geochemical investigations at the Mavro Xylo deposit, which led to the identification of Ag-rich Mn-Zn±Pb vein-type mineralization. The studied paragenesis appears to have developed during two hydrothermal stages: stage I, characterized by the mineral assemblage rhodonite–quartz–rhodochrosite–pyrophanite–pyrite–galena–Te bearing argentite–sphalerite–wurtzite–alabandite, and stage II, dominated by Ag-rich, Mn-Zn±Pb oxides in the form of fracture-fills along a high-angle NE-SW fault zone in brecciated marbles. Bulk analyses of the stage-II oxide assemblage yielded concentrations of Ag up to 0.57 wt.%. In the veins, wurtzite is present in bands, succeeded by manganese oxides, while calcite and quartz are the main gangue minerals. We placed particular emphasis on the occurrence of Ag in high concentrations within distinct manganese oxides. Major silver carriers include Zn-bearing todorokite, chalcophanite, and hydrous Pb-Mn oxide. The vein-type mineralization at Mavro Xylo shares many characteristics with other intermediate-sulfidation epithermal precious metal-rich deposits associated with high Mn concentrations. The evolution of the mineral paragenesis indicates a change in the physicochemical attributes of the ore-forming fluids, from initially reducing (stage I) to oxidizing (stage II). Although the origin of the initial ore-forming fluid remains to be constrained, the above redox change is tentatively attributed to the increasing incursion of meteoric waters over time.
Discovered within the North Himalayan Metallogenic Belt (NHMB), the Zhaxikang Pb–Zn–Ag–Sb deposit stands as the sole super-large scale ore deposit in the region. This deposit holds significant quantities of Pb and Zn (2.066 million tons at 6.38% average grade), Ag (2661 tons at an average of 101.64 g/t), and Sb (0.235 million tons at 1.14% average grade), making it one of China’s foremost Sb–polymetallic deposits. Stibnite represents the main carrier of Sb in this deposit and has been of great attention since its initial discovery. However, the trace element composition of stibnite in the Zhaxikang deposit has not yet been determined. This study carried out an analysis of the distribution patterns and substitution processes of trace elements within stibnite gathered from the Zhaxikang deposit, aiming to provide crucial information on ore-forming processes. Utilizing high-precision laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS), we discovered that the studied stibnite is notably enriched in arsenic (~100 ppm) and lead (~10 ppm). Furthermore, the notably consistent time-resolved profiles suggest that elements such as Fe, Cu, As, In, Sn, Hg, and Pb predominantly exist as solid solutions within stibnite. Consequently, it is probable that the enrichment of Cu, Pb, and Sn in stibnite is due to isomorphic substitution reactions, including 3Pb2+↔2Sb3+, Cu+ + Pb2+↔Sb3+, and In3+ + Sn3+↔2Sb3+. Apart from that, Mn, Pb, and Hg with the spiky signals indicate their existence within stibnite as micro-inclusions. Overall, we found that the trace element substitutions in stibnite from the Zhaxikang Pb–Zn–Ag–Sb deposit are complicated. Incorporations of trace elements such as Pb, Cu, and In into stibnite are largely influenced by a variety of factors. The simple lattice structure and constant trace elements in studied stibnite indicate a low-temperature hydrothermal system and a relatively stable process for stibnite formation.
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