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The newly discovered Xiaohongshilazi deposit located in Panshi City, central Jilin Province, NE China, is a medium-scale Pb–Zn–(Ag) deposit. The Pb–Zn–(Ag) orebodies are divided into layered and vein-type orebodies, which have different ore geneses. The layered Pb–Zn orebodies are mainly hosted within and spatially controlled by the volcanic rocks. To constrain the age and tectonic setting of the layered Pb–Zn mineralization, we completed laser-ablation–ICP–MS zircon U–Pb dating and whole-rock major and trace element analyses of the ore-bearing volcanic rocks. The dacite samples were confirmed as belonging to the Daheshen Formation and were the main ore-bearing volcanic rocks for the layered orebodies. They yielded concordia U–Pb ages of 278.1 ± 1.8 Ma and 278.3 ± 1.8 Ma, respectively, indicating that the volcanic rocks from the Daheshen Formation and related layered Pb–Zn mineralization were formed in the early Permian. The andesite and rhyolite located above the layered orebodies yielded concordia U–Pb ages of 225.0 ± 1.1 Ma, 225.3 ± 1.5 Ma, and 224.7 ± 1.2 Ma, respectively; these substances are considered to be of the Sihetun Formation and were first reported in the area. The dacite samples associated with layered Pb–Zn mineralization were high in SiO₂ (62.54–65.02 wt.%), enriched in LREEs and LILEs (e.g., Rb, Ba, and K), and showed depletion in HFSEs (e.g., P and Ti). It showed slightly negative Eu anomalies (δEu = 0.60–0.65) and negative Nb anomalies, with Th/Nb (1.12–1.21) and La/Nb (2.8–4.7) ratios, presenting subduction-related arc magma affinity formed in an active continental margin setting. In agreement with previous studies on zircon Hf isotopes (ε_Hf (t) = +0.23~ +10.60) of the volcanic rocks from the Daheshen Formation, we infer that they were derived from the partial melting of the depleted lower crust. In conclusion, mineralization characteristics, geochronological data, geochemical features, and regional tectonic evolution suggest that two Pb–Zn–(Ag) mineralization stages from the Xiaohongshilazi deposit occurred: the layered VMS-type Pb–Zn mineralization associated with the marine volcanic rocks from the early Permian Daheshen Formation, which was induced by the subduction of the Paleo-Asian oceanic plate beneath the northern margin of the North China Craton, and the vein-type Pb–Zn–(Ag) mineralization caused by the subduction of the Paleo-Pacific Plate in the early Jurassic. Considering this, along with the mineralization characteristics of the same-type polymetallic deposits in this region, we propose that the early Permian marine volcanic rocks have great prospecting potential for the VMS-type Pb–Zn polymetallic deposits. Full article

The Beiwagou Pb-Zn deposit, located in the western part of the Liaodong Peninsula, is a carbonate-hosted stratiform deposit with a Pb + Zn reserve of 0.08 Mt @ 4.14% (Pb + Zn). The orebodies occur as conformable layers and lenses and are strictly controlled by strata (the Paleoproterozoic Gaojiayu and Dashiqiao Formations) and lithology (plagioclase amphibolite and dolomitic marble). Given that previous studies have focused only on the mineralization features and mineralogy of deposits, herein, we report in situ trace element analyses of pyrite using LA-ICP-MS, together with in situ sulfur isotopes of pyrite, to constrain the composition, substitution mechanisms, source of sulfur, and sulfate reduction pathways of pyrite in the Beiwagou deposit. Based on pyrite morphology, texture, and chemistry, four pyrite types were identified: subhedral, porous-to-massive pyrite (Py1) related to chalcopyrite; subhedral, porous crushed pyrite (Py2) associated with fine-grained sphalerite; rounded and porous pyrite (Py3) related to the Zn-rich part of the laminated ore; and anhedral, porous-to-massive pyrite (Py4) associated with pyrrhotite, arsenopyrite, sphalerite, and galena. Py1 is characterized by high As, Ag, Cd, In, Au, Cu, and Zn concentrations and low Te, Bi, and Mo concentrations, whereas Py2 has high concentrations of Co and Ni and low concentrations of other trace elements, such as Cu, Zn, Bi, and Te. Py3 is characterized by elevated As concentrations, low Co, Ni, In, W, Te, and Tl concentrations, and varying Pb concentrations, whereas Py4 has low Ag, Cd, In, Zn, Cu, and Mn concentrations and varying W, Co, Ni, Pb, Sb, and As concentrations. Significant correlations between some elements in each pyrite type suggest substitution mechanisms, such as (Zn²⁺ + Cu²⁺ + Mn²⁺ + Cd²⁺) ↔ 2Fe²⁺, Ag⁺ + (Sb)³⁺ ↔ 2Fe²⁺, and (Te⁺ + Ag⁺) + Sb³⁺ ↔ 2Fe²⁺, and the existence of a negative correlation between Co and Ni implies competition between both elements. The strongly positive δ³⁴S values (12.11‰–23.54‰) are similar to that of seawater sulfates and likely result from thermochemical sulfate reduction (TSR). In conclusion, the Beiwagou Pb-Zn deposit is a typical SEDEX deposit and mineralization likely occurred during diagenesis. Full article

The Uragen giant sandstone-hosted Zn–Pb deposit has a proven reserve of 5.90 Mt metals in the southern ore zone and potentially 10 Mt metals for the whole deposit, and orebodies are strictly confined to the bleached clastic rocks of the Lower Cretaceous red beds. The bleaching has been used to guide lead–zinc exploration; however, its nature and origin, as well as the relationship with Zn–Pb mineralization, remains unclear, although it is closely related to regional oil–gas infillings. Detailed field investigation and petrographic observation, TESCAN-integrated mineral analyzer (TIMA), and X-ray fluorescence (μ-XRF) analysis of the red and bleached sandstone at the same sedimentary layer demonstrate that the bleaching is mainly caused by the reductive dissolution of hematite pigment, which probably resulted from the interaction with H₂S formed by in situ sulfate reduction during hydrocarbon migration. The calcite cements in the bleached sandstones show δ¹³C and δ¹⁸O values of −5.36~−5.94‰ and 20.94~27.91‰, respectively, and these samples fall close to the evolution line of decarboxylation of organic matter in δ¹³C-δ¹⁸O diagram, also suggesting a genetic relationship between the bleaching and hydrocarbon-bearing fluids. Petrol–mineral composition changes and sulfide characteristics of red, bleached, mineralized zones, as well as pyrite locally replaced by coarse-grained galena in the mineralized zone, imply that the bleaching may occurred before Zn–Pb mineralization. Mass balance calculation and μ-XRF analysis indicate that large amounts of Fe and minor Zn were extracted from red beds with little or no sulfates; however, the red beds with abundant sulfates may be a sink for leached ore metals during the bleaching process. We therefore propose that the former accumulations of iron sulfides and reduced sulfur in the bleached zones may provide an ideal chemical trap for later Zn–Pb mineralization, and the bleached zones with high ∑S contents are the favorable prospective targets of the Uragen-style sandstone-hosted Zn–Pb deposits. Full article

A crystal-chemical study of historical specimens as well as new ones belonging to the jordanite–geocronite series from the Pollone baryte + pyrite ± (Pb-Zn-Ag) ore deposit (Valdicastello Carducci, Apuan Alps, Tuscany, Italy) has been performed. These crystals were collected in quartz extension veins embedded in three different occurrences: (i) baryte + pyrite orebodies; (ii) schist layers interbedded between baryte + pyrite orebodies; and (iii) schists at the contact with pyrite-poor baryte orebodies. Electron-microprobe data indicated the occurrence of three distinct groups of compositions within the sample suite. These correspond to As-bearing geocronite, Sb-rich jordanite, and Sb-bearing jordanite, with mean compositions Pb₁₄Sb_3.8As_2.2S₂₃, Pb₁₄Sb_2.9As_3.1S₂₃, and Pb₁₄Sb_2.6As_3.4S₂₃, respectively. Crystals representative of these different compositions have been investigated through single-crystal X-Ray diffraction studies and their crystal structures have been solved to R₁ = 0.078, 0.069, and 0.033, respectively. The unit-cell volume decreases passing through As-bearing geocronite (V = 2149.5(3) ų) to Sb-bearing jordanite (V = 2132.3(3) ų). The As-to-Sb substitution takes place preferentially at the Sb4 site; through the increasing of the Sb content, Sb can substitute As also at the As6 site. According to the structural study of the ore deposit, formation of jordanite–geocronite is subordinated to a late Alpine deformative D₂ stage, which permitted in situ remobilization of preexisting sulfide ore in small quartz extension veins. Such a local recrystallization would explain the variability of the As/(As + Sb) ratio of the members of the jordanite series, reflecting the heterogeneity of the orebody. Full article