Search Results (24)

Jurassic–Cretaceous marine–continental carbonate–evaporitic sequences in the Neuquén Basin of Argentina host numerous stratabound Ba–Sr deposits. Mineralization (Sr–barite, Ba–celestine, and minor Pb–Zn–Cu–Fe sulphides) occurs as bedding parallel lenses and crosscutting veins. The stratiform mineralization is formed by replacements of carbonate and gypsum beds and often exhibits typical zebra textures. Dissolution processes associated with Neogene regional uplift produced karstic cavities where a new generation of barite was deposited. Regionally, W to E distribution of carbonates/evaporites and that of Ba–Sr deposits is coincidental. Lower Cretaceous Sr–Ba deposits are spatially related to large N-S reverse faulting, frequently limited to the eastern limb of the folded structures. Average δ¹⁸O and δ³⁴S of stratiform and crosscutting vetiform mineralization do not differ significantly, suggesting a common source of sulphate and cations. Deposits spatially linked to areas with magmatic activity and those that are not have similar isotopic values, compatible with bacterial and/or thermochemical reduction of contemporaneous seawater sulphate, although sulphides only occur in deposits with evidence of nearby magmatic activity. Thermal convection of basinal brines leached metals from the Mesozoic sedimentary pile; Ba and Sr were extracted from siliciclastic and carbonate rocks, and sulphur from evaporite layers. Fluids related to Tertiary magmatism helped producing an epithermal mineral association composed of barite, quartz, adularia, and minor sulphides/sulphosalts hosted by veins. Arroyo Nuevo mine (Ba) is different, as it seems to be the product of hydrothermal SedEx deposition onto the anoxic seafloor. Full article

The Sichuan–Yunnan–Guizhou Pb-Zn metallogenic belt (SYG metallogenic belt), a crucial metallogenic unit on the southwestern margin of the Yangtze Block, is a key part of the South China low-temperature metallogenic domain. The incorporation mechanisms and distribution of trace elements (e.g., Ge, Ga, Cd) widely enriched in Pb-Zn sulfides throughout this region remain poorly understood. This study investigates main-ore-stage sulfides (sphalerite and pyrite) from the Maoping Pb-Zn deposit using in situ laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) analyses and mapping to systematically elucidate the partitioning and occurrence of these trace elements. The key findings are as follows: (1) Sulfides show distinct elemental partitioning: sphalerite preferentially concentrates Cd, Ag, Ge, Ga, and Se, whereas pyrite is significantly enriched in Mn, Ni, As, and Co. (2) Sphalerite is the primary host for many trace elements. Cadmium, Ge, Mn, Cu, and Ag mainly enter the sphalerite lattice by substituting for Zn²⁺. Coupled substitution mechanisms, such as Zn²⁺ ↔ Cd²⁺, 2Zn²⁺ ↔ Ge²⁺ + Cu²⁺, and 2Zn²⁺ ↔ Ga³⁺ + Cu⁺, facilitate the incorporation of Ge and Ga. (3) The sphalerite exhibits a trace element assemblage of high Cd-Ge and low Fe-Mn, which is geochemically similar to typical Mississippi Valley-type (MVT) deposits and differs significantly from sedimentary exhalative (SEDEX) and magmatic–hydrothermal deposits, indicating a medium- to low-temperature metallogenic environment. Based on these geochemical signatures and epigenetic textures, we confirm that the Maoping Pb-Zn deposit exhibits similarities with MVT deposits. Nevertheless, distinct differences in the tectonic setting and metal grades suggest it is a unique SYG-type Pb-Zn deposit. Full article

This study critically examines the early Cretaceous carbonate-hosted Zn-Pb (±Ba±Cu) deposits of the Malayer-Esfahan (MEMB) and Yazd-Anarak (YAMB) metallogenic belts in Iran, which have been inaccurately classified as Mississippi Valley type (MVT) deposits by Nejadhadad et al. (2025). Our findings reveal significant differences in mineralogy, fluid inclusion characteristics, and geochemical signatures compared to typical MVT deposits. These deposits are more akin to Irish-type Zn-Pb mineralization and formed in extensional and passive margin environments around the Nain–Baft back-arc basin. The normal faults in this back-arc rift can transform significantly during inversion and compressional tectonics, reactivating to behave as reverse faults and leading to new geological structures and landscapes. Our study highlights barite replacement as a crucial factor in forming sediment-hosted Zn-Pb (±Ba±Cu) and barite-sulfide deposits. Based on textural evidence, fluid inclusion data, and sulfur isotope analyses, we propose that barite plays a fundamental role in controlling subsequent Zn-Pb (±Ba±Cu) mineralization by serving as both a favorable host and a significant sulfur source. Furthermore, diagenetic barite may act as a precursor to diverse types of sediment-hosted Zn-Pb (±Ba±Cu) mineralization, refining genetic models for these deposits. Sulfur isotope analyses of Irish-type deposits show a broad δ³⁴S range (−28‰ to +5‰), indicative of bacterial sulfate reduction (BSR). Nevertheless, more positive δ³⁴S values (+1‰ to +36‰) and textural evidence in shale-hosted massive sulfide (SHMS) deposits suggest a greater role for thermochemical sulfate reduction (TSR) in sulfide mineralization. Full article

Regionally metamorphosed, Neoproterozoic stratiform baryte deposits near Aberfeldy in the Grampian Highlands of Scotland, UK, contain barium-poor and barium-rich micas in the host rocks and mineralized strata, respectively. The barium-rich micas include muscovite, biotite, phlogopite, and chromium-bearing muscovite. They occur in schistose metasediments and metabasites, in barium-feldspar rocks, and in small amounts in baryte rock. An extensive study of micas in a range of lithologies using electron-probe micro-analysis found up to 10.86 wt% BaO in muscovite, 5.46 wt% in biotite, and 15.70 wt% in Ba-Cr muscovite, the latter containing up to 9.27 wt% Cr₂O₃. Compositions are comparable with Ba- and Ba-Cr-micas in other metamorphosed Sedimentary Exhalative deposits and barium-rich metasediments worldwide. In one baryte rock sample, disseminated crystals of an exotic Ba-V-Cr mica contain up to 12.33 wt% BaO and 10.82 wt% V₂O₃, compositionally similar to Ba-V micas in the Hemlo lode gold deposit, Ontario. Ba²⁺ incorporation is mainly by coupled substitution with Al³⁺ for K⁺ + Si⁴⁺ in the tetrahedral site. The extent of phengitic (Tschermakitic) substitution is typical of micas in amphibolite-facies metasediments. Similar Fe:Mg ratios in coexisting muscovite and biotite reflect partitioning of iron into sulphides and metamorphic equilibration, with rare exceptions in fine-grained rocks that exhibit millimetre-scale disequilibrium. Full article

Siderite and baryte are common non-sulphide phases in sedimentary exhalative (SEDEX) deposits, but their formation remains poorly understood. Siderite is important as an exploration vector in some deposits, whereas baryte is important as a S source in some deposits. The past-producing Walton deposit (Nova Scotia, Canada) consists of two ore types: (1) a sulphide body primarily hosted by sideritised Viséan Macumber Formation limestone (0.41 Mt; head grade of 350 g/t Ag, 4.28% Pb, 1.29% Zn, and 0.52% Cu), and (2) an overlying massive baryte body of predominantly microcrystalline baryte (4.5 Mt of >90% baryte). This study used optical microscopy, SEM-EDS, cathodoluminescence (CL), LA-ICP-MS, and SIMS sulphur isotope analysis of siderite and baryte to elucidate their origin and role in deposit formation. Siderite replaces limestone and contains ≤9 wt. % Mn, is LREE-depleted (PAAS-normalised REEY diagrams), and has low (<20) Y/Ho ratios. Sideritisation occurred due to dissimilatory iron reduction (DIR) that led to the breakdown of Fe-Mn-oxyhydroxides and organic matter, as indicated by light δ¹³C_VPBD values and negative Y anomalies. The baryte body is dominated by a microcrystalline variety that locally develops a radial texture and coarsens to a tabular variety; it also occurs intergrown with, and as veins in, massive sulphides. Based on fluid inclusion data from previous studies, the coarser baryte types grew from a hot (>200 °C) saline (25 wt. % NaCl) fluid containing CO₂-CH₄ and liquid petroleum. Marine sulphate δ³⁴S_VCDT values typical of the Viséan (~15‰) characterise the baryte body and some tabular baryte types, whereas heavier (~20‰) and lighter (~10‰) values typify the remaining tabular types. The variations in tabular baryte relate to distinct zones identified by CL imaging and are attributed to the sulphate-driven anaerobic oxidation of methane (SDAOM) and oxidation of excess H₂S after sulphide precipitation. These results highlight the importance of hydrocarbons (methane and organic matter) in the formation of both the siderite and the baryte at Walton and that DIR and the SDAOM can be important contributing processes in the formation of SEDEX deposits. Full article

The Huaniushan lead–zinc–silver deposit is a hydrothermal sedimentary exhalative deposit (SEDEX), and the mining area has complex geological conditions, with the main tectonic structure being the Huaheitan–Shuangfengshan Fault (F₃), which controls the distribution of strata and magmatic rocks. Since the discovery of the Huaniushan lead–zinc–silver deposit, diverse interpretations of its genesis and metallogeny have been proposed, making it challenging to establish a definitive geological explanation. Moreover, using a single geophysical exploration method relies on limited rock physical parameters, making it difficult to effectively characterize underground structures. The combined use of multiple geophysical methods can effectively integrate the geophysical characteristics of different rock physical parameters, reducing the multiplicity and uncertainty of the inverse interpretation of geophysical data. The comprehensive interpretation of three-dimensional inversion based on various geophysical data, the construction of geological–geophysical models on geological grounds, the establishment of hidden ore exploration and positioning, and the rapid evaluation of geophysical technological systems are the current research trends in mineral exploration. In light of this, in this study, we conducted research on the three-dimensional inversion interpretation of gravity and magnetoelectric exploration data of the Huaniushan sedimentary exhalative lead–zinc–silver polymetallic deposit and constructed a three-dimensional geological–geophysical model of the study area based on the obtained three-dimensional physical structure of the underground density, magnetization intensity, resistivity, and polarizability of the study area, in combination with related geological and drilling hole data. Finally, we comprehensively interpreted the favorable mineralization sites in the study area. Full article

Background/Objectives: This study compared two pilot scale continuous manufacturing methods of solid self-emulsifying drug delivery systems (SEDDSs) via hot melt extrusion (HME). Methods: A model poorly water-soluble drug carvedilol in low dose (0.5–1.0% w/w) was processed in HME either in a conventional powder form or pre-dissolved in the liquid SEDDS. Results: HME yielded a processable final product with up to 20% w/w SEDDS. Addition of carvedilol powder resulted in a non-homogeneous drug distribution in the extrudates, whereas a homogeneous drug distribution was observed in pre-dissolved carvedilol. SEDDSs were shown to have a plasticizing effect, reducing the HME process torque up to 50%. Compatibility between excipients and carvedilol in the studied ratios after HME was confirmed via DSC and WAXS, demonstrating their amorphous form. Solid SEDDSs with Kollidon^® VA64 self-emulsified in aqueous medium within 15 min with mean droplet sizes 150–200 nm and were independent of the medium temperature, whereas reconstitution of Soluplus^® took over 60 min and mean droplet size increased 2-fold from 70 nm to 150 nm after temperature increased from 25 °C to 37 °C, indicating emulsion phase inversion at cloud point. Conclusions: In conclusion, using Kollidon^® VA64 and pre-dissolved carvedilol in SEDDS has shown to yield a stabile HME process with a homogenous carvedilol content in the extrudate. Full article

Bedded barite, Fe-Zn-Pb sulfides, carbonates, and cherts within Ediacaran (Dalradian Supergroup) graphitic metasediments near Aberfeldy in Scotland have previously been interpreted as chemical sediments precipitated from hydrothermal fluids episodically exhaled into marine basins filled with organic-rich mud, silt, and sand. Lithological variation and compositional diversity in pyrite and sphalerite reflect varied redox environments and proximity to hydrothermal discharges. Thick beds (>2 m) of barite have relatively uniform δ³⁴S of +36 ± 1.5‰, considered to represent contemporaneous seawater sulfate, as negative Δ¹⁷O indicates incorporation of atmospheric oxygen during precipitation in the water column. However, certain features suggest that diagenetic processes involving microbial sulfate reduction modified the mineralogy and isotopic composition of the mineralization. Barite bed margins show decimeter-scale variation in δ³⁴S (+32 to +41‰) and δ¹⁸O (+8 to +21‰), attributed to fluid-mediated transfer of dissolved barium and sulfate between originally porous barite and adjacent sediments, in which millimetric sulfate crystals grew across sedimentary lamination. Encapsulated micron-sized barium carbonates indicate early diagenetic barite dissolution with incorporation of sulfur into pyrite, elevating pyrite δ³⁴S. Subsequently, sulfidation reactions produced volumetrically minor secondary barite with δ³⁴S of +16 to +22‰. Overall, these processes affected small volumes of the mineralization, which originally formed on the seafloor as a classic SEDEX deposit. Full article

Iran hosts more than 350 Precambrian to Cenozoic sediment-hosted Zn-Pb±Ba and barite-sulfide deposits, including shale-hosted massive sulfide (SHMS, also called SEDEX) and Irish-type and Mississippi Valley-type (MVT) mineralization, and barite is a common mineral in these deposits. In the SHMS deposits, barite is typically found as fine-grained disseminations in thin laminae. In these deposits, the sulfide laminae often occur as diagenetic replacements and as bands containing authigenic and diagenetic barite and pyrite framboids. In the Irish-type Zn-Pb-Ba and stratabound barite-sulfide deposits, barite exhibits various textures, including fine-grained disseminated barite, banded zebra textures, veins, and massive barite lenses. In some of the giant Irish-type deposits, as well as in the stratabound barite-sulfide mineralization, the main stratabound sulfide ore is developed within a barite envelope and is characterized by the replacement of barite and pyrite by chalcopyrite, galena, and sphalerite. In the MVT deposits, the formation of barite is often related to dolomitization, and sulfide mineralization involves the replacement of the dolomitized carbonate rocks, as well as associated barite. Fluid inclusion studies on the Irish-type deposits indicate that the temperatures and salinities of the sulfide-forming fluids are higher compared to those of the barite-forming fluids. Fluid inclusion analyses of coarse-grained barites from Irish and MVT deposits reveal their hydrothermal origin. The δ³⁴S values of sulfide minerals (pyrite, sphalerite, and galena) in Irish-type deposits exhibit a broad range of low values (mostly −28 to +5‰), primarily revealing a process of bacterial sulfate reduction (BSR). However, the textures (replacement, colloform, and banded) and more positive sulfur isotope values (+1 to +36‰) in the SHMS Zn-Pb deposits suggest that bacterial sulfate reduction (BSR) plays a less significant role. We suggest that thermochemical sulfate reduction (TSR) connected to the direct replacement of barite plays a more relevant role in providing sulfur for the sulfide mineralization in the SHMS, barite-sulfide, and MVT deposits. Based on the textual evidence, sulfur isotopic data, and fluid inclusion studies, barite has been identified as a key controller for the subsequent Zn-Pb mineralization by providing a suitable host and significant sulfur contribution in the sediment-hosted Zn-Pb and stratabound barite-sulfide deposits. This implies that diagenetic barite might be a precursor to all types of sediment-hosted Zn-Pb mineralization. Full article

The large Dongtangzi Zn-Pb deposit is located in the southwest of the Fengxian–Taibai (abbreviated as Fengtai) ore cluster in the west Qinling orogen. The origin of the deposit is controversial, positing diverse genesis mechanisms such as sedimentary-exhalative (SEDEX), sedimentary-reformed, and epigenetic-hydrothermal types. This study combines systematic ore geology observations with high-precision Rb-Sr and Sm-Nd ages of 211 Ma and in situ S-Pb isotopes to constrain the timing and origin of mineralization. In situ S-Pb isotopic studies show that the sulfide ores display a narrow range of δ³⁴S values from 1.1‰ to 10.2‰, with ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb, and ²⁰⁸Pb/²⁰⁴Pb ratios of 18.07 to 18.27, 15.64 to 15.66, and 38.22 to 38.76, respectively. On the other hand, pyrites of the sedimentary period and the granite porphyry dike have δ³⁴S values ranging from 15.8 to 21.4‰ and from 2.1 to 4.3‰ (with ²⁰⁶Pb/²⁰⁴Pb ratios of 18.09 to 18.10, ²⁰⁷Pb/²⁰⁴Pb ratios of 15.59 to 15.61, and ²⁰⁸Pb/²⁰⁴Pb ratios of 38.17 to 38.24), respectively. The above-mentioned S-Pb isotopic compositions indicate that the metallic materials involved in ore formation originated from a mixture of Triassic magmatic hydrothermal fluid and metamorphic basement. By integrating the regional geology, mineralization ages, and S-Pb isotopic studies, we propose that the Dongtangzi Zn-Pb deposit is the product of epigenetic hydrothermal fluid processes, driven by Late Triassic regional tectono-magmatic processes. Full article

Understanding the phosphorus (P) cycle is essential for preventing soil P loss, improving environmental quality, and promoting sustainable agriculture, particularly in urban areas. In this study, a representative city of the lower Yangtze River Basin, Nanchang, was chosen to systematically explore the distribution and transformation of soil P forms, which were extracted by an improved SEDEX method and measured by a standard phosphorus–molybdenum blue method under three land use patterns. The contents of soil P forms were the highest in the dryland and the lowest in the paddy field, with total P accumulation in the upper wasteland and paddy field soils but in the lower dryland soil. The pH value and grain size affected soil P form distributions to a variable extent from one land use pattern to another. The transformation of soil P forms was weak in the wasteland. It was first found that some detrital limestone P (De-P) was transformed into exchangeable P (Ex-P) in the paddy field with authigenic calcium-bound phosphorus (Au-P) and organic phosphorus (OP) transformation, and the transformation between Ex-P and iron-bound phosphorus (Fe-P), Au-P, and between Au-P and OP existed in the dryland. Land use pattern was the dominant driver for the P distribution and transformation of soil P. This study highlights the critical role of land use patterns in affecting the P cycle of soils in urban areas and the importance of sustainable urban land management. Full article

Quantifying and identifying the introduction of metal in ore deposits that have experienced multiple overprinting hydrothermal events remains an elusive yet essential goal in metallogenic studies. Here, we constrain the origin of Co in the Idaho Cobalt Belt (ICB) that experienced two distinct metal-rich events that introduced Co and Cu. We performed a detailed petrographic study of sulfide ore at Iron Creek in the ICB, in concert with the quantification of trace metal element concentrations and copper isotope values to identify the introduction of Co in the system. The pyrite displays various degrees of alteration, with the highest Co concentrations (up to 6 wt.%) in less-altered pyrite grains (e.g., sharp edges, absence of altered boundaries and fissures) and highest δ⁶⁵Cu isotope value. The most-altered pyrite grains (e.g., corroded grains, round and altered boundaries) have lower Co contents and lower δ⁶⁵Cu isotope values that match the copper isotope values of the chalcopyrite. The least-altered pyrite shows a narrow δ⁶⁵Cu range between −0.39‰ to −0.58‰. In contrast, the most-altered pyrite grains are isotopically depleted, showing a δ⁶⁵Cu range from −1.35‰ to −0.90‰. Chalcopyrite shows a δ⁶⁵Cu range between −1.07‰ and −0.77‰. We interpret, from the Cu isotope compositions and Co concentrations in pyrite, that the Co was originally introduced into the siliciclastic host rock package in a Mesoproterozoic SEDEX environment. The heavier Cu was then preferentially leached in a second event, resulting in isotopically lighter Cu in the altered pyrite. Remobilization of the SEDEX cobalt was likely associated with CO₂-rich metamorphic fluids present in the region during the Mesoproterozoic East Kootenay orogeny, the late Mesoproterozoic Grenville orogeny, and the Late Jurassic to Late Cretaceous Cordilleran orogeny. Full article

Supergene hydrous sulfate minerals form through the oxygenation and weathering of primary sulfides. In the Qinghai–Tibet Plateau region, with an alpine and dry environment, hydrous sulfate minerals oxidized from pyrite-bearing ore bodies provide important clues regarding the mineralization and environment. The Tuolugou sedimentary-exhalative (SEDEX) Co-Au deposit is located in the East Kunlun metallogenic belt of the northern Qinghai–Tibet Plateau in China. In the mining district, pyrite is the prevalent Co-hosting sulfide mineral, and is partially exposed on the surface to weathering and oxidation. Herein, we document the mineral assemblages in the supergene oxidation zone in the Tuolugou deposit, probe the genesis of supergene assemblage, and explore the implications for exploration. Three zones can be recognized in the oxidation zone of the Tuolugou deposit, including the outer zone (natrojarosite), intermediate zone (rozenite and aplowite), and inner zone (roemerite and melanterite). The mechanism of oxidation under aerobic and anaerobic conditions, as well as zoning with different oxidation degrees, are described in detail. Hydrous sulfates such as natrojarosite can be used as possible indicators of the exploration of albitite-related SEDEX deposit in this region. 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

China, Vietnam, Brazil, and Russia have the largest deposits of rare earths. However, in recent works, the occurrence of light rare earth elements has been demonstrated in an exhalative sedimentary type mineral (SEDEX) in Mexico, with adequate Ce and Nd contents. Additionally, it is this mineral that has been used to study the cation exchange capacity of non-metallic minerals and organic materials, such as bentonite, diatomite, and eggshell. To carry out this work, the crushed and ground SEDEX ore was leached using HCl, H₂SO₄, and HNO₃. Subsequently, the liquid containing the Ce and Nd ions extracted from the mineral was put in contact with the respective ion exchangers, evaluating the effect of temperature and pH to determine the cation exchange efficiency of each exchanger tried. It was found that the best leaching results were achieved with the H₂SO₄, obtaining an extraction of Ce and Nd of 97.6% and 95.7%, respectively. On the other hand, in the case of cation exchange, the best results found for the extraction of Ce and Nd were using diatomite at a temperature of 323 K and a pH of 3, obtaining an extraction of 99.06% Ce and 99.07% Nd. Full article