Source Of Ore-forming Fluids Research Articles

Source of Ore-Forming Fluids and Ore Genesis of the Batailing Au Deposit, Central Jilin Province, Northeast China: Constraints from Fluid Inclusions and H-O-C-S-Pb Isotopes

The Batailing Au deposit is a vein-type deposit in central Jilin Province, situated in the southern sector of the Lesser Xing’an–Zhangguangcai Range within the eastern Central Asian Orogenic Belt. NE-trending fault-controlled orebodies occur in the Upper Permian Yangjiagou Formation and quartz diorite–porphyrite. The mineralisation process was delineated into three stages: (I) quartz–arsenopyrite–pyrite, (II) quartz–polymetallic sulphides (main Au mineralisation stage), and (III) quartz–pyrite–carbonate. Fluid inclusions (FIs) in quartz were identified as four types: PC-type (pure CO2), C1-type (CO2-bearing), C2-type (CO2-rich), and W-type (aqueous two-phase). Raman spectroscopy analysis revealed that the vapor components of the FIs predominantly comprised CO2 with minor quantities of CH4 in stages I–II. Stages I and II encompassed four types of FIs with homogenisation temperature ranging from 264 to 332 °C and 213 to 292 °C and salinity spanning from 4.7 to 11.2 wt% and 1.8 to 11.6 wt%, respectively. Stage III exclusively contained W-type FIs with homogenisation temperature ranging from 152 to 215 °C and salinity spanning from 1.4 to 6.4 wt%. H-O isotopic values (δD = −84 to −79.6‰, δ18OH2O = 6.2 to 6.4‰ in stage I and δD = −96.4 to −90.4‰, δ18OH2O = 2.8 to 4.4‰ in stage II) and microthermometric data indicated that the ore-forming fluids are initially from a magmatic source, with later meteoric water input. Low C isotopic data from CO2 in FIs in quartz (−24.4 to −24.3‰ in stage I and −23.7 to −22.6‰ in stage II) indicated an organic carbon source. Ore precipitation is mainly attributable to fluid immiscibility. S-Pb isotopic data (δ34S = −3.5 to −1.6‰; 206Pb/204Pb = 18.325–18.362, 207Pb/204Pb = 15.523–5.562, 208Pb/204Pb = 38.064–38.221) revealed that ore metals primarily originated from magma. Based on this research, the origin of the Batailing Au deposit is of the mesothermal magmatic–hydrothermal lode type.

Genesis studies of Li–Rb deposits in pegmatites from Bailongshan, western China: Evidence from chronology, fluid inclusions, and H–O isotope analysis

The Bailongshan Pegmatite deposit, located in the West Kunlun Orogenic Belt, Northwest China, is a newly discovered, super-large Li–Rb (Be–Ta–Nb) rare-metal deposit. Since complex magmatic-hydrothermal processes are responsible for the mineralization of such rare-element pegmatites, it is desirable to study the evolution and sources of ore-forming fluids to analyze the genesis of ore deposits. In this study, the 40Ar/39Ar plateau ages of muscovite and biotite were determined to be 171.36 ± 1.87 and 172.39 ± 1.66 Ma, respectively, indicating that the duration of hydrothermal mineralization was approximately 170 Ma. Based on the zonal nature of the mineral assemblage, the Bailongshan area was divided into four zones and stages (I–IV), namely the albite–quartz–lithium tourmaline (AQT, stage I), albite–quartz-bearing mica (AQM, stage II), albite–quartz–spodumene (AQS, stage Ⅲ), and spodumene–quartz (SQ, stage IV) zones. Among these, AQS and SQ were the main ore-bearing areas. In terms of the fluid inclusions found in quartz and spodumene, the different types include a gas-rich phase (V-type), a liquid-rich phase (L-type), a daughter mineral-bearing three-phase (S-type), and a carbon dioxide-bearing phase (C-type). In stage I, the homogeneous temperatures of the V- and S-type fluid inclusions varied from 365 to 415 °C, while their corresponding salinities were 8.5–12.9 and 44.8–47.2 wt% NaCl equiv., respectively. In stage II, the homogeneous temperature and salinity of the L-type inclusions were 315–365 °C and 9.9–13.3 wt% NaCl equiv., respectively, while in stages Ⅲ and IV, the homogeneous temperatures of the L- and S-type fluid inclusions were between 235 and 335 °C, while their salinities were 7.2–12.3 and 32.1–37.0 wt% NaCl equiv., respectively. Furthermore, for the C-type inclusions, the homogeneous temperature and salinity were 235–320 °C and 4.9–10.6 wt% NaCl equiv., respectively. The laser Raman results showed that the fluid in the metallogenic stage was an H2O–NaCl–CO2–CH4 system. Based on the homogeneous temperature and salinity results, the fluid capture pressure from stage III to stage IV was calculated to be 280–150 MPa, and the depth of the capture was >6 km. Moreover, the H–O isotope results suggested that the early ore-forming fluids are mainly magmatic hydrothermal fluids, whereas the later (stage IV) mineralizing fluids may be mixed with a small amount of meteoric water. The subsequent immiscibility of the fluid may be one of the factors responsible for the discharge and precipitation of minerals.

Fluid inclusion and He-Ar-Pb isotope studies of the Dabie-type Leimengou giant porphyry Mo deposit, Qinling Orogen

The Leimengou deposit is a Dabie-type porphyry Mo system in the Leimengou-Qiyugou orefield of Qinling Orogen. Orebodies host within the porphyry and the metasedimentary Taihua Supergroup. However, the characteristics and sources of ore-forming fluid, metal precipitation mechanism, and the sources of mineralizing substances remain unclear. In this contribution, by a comprehensive study comprising an investigation of deposit geology, fluid inclusion microthermometry, and He-Ar-Pb isotope, we discuss the source and evolution of ore-forming fluids and the molybdenum precipitation mechanism of the Leimengou deposit. The mineralizing process is divided into the Stage I quartz ± K-feldspar vein in potassic altered zone, Stage IIa molybdenite ± quartz vein, and Stage IIb molybdenite + quartz + pyrite ± purple fluorite vein in silicification-phyllic altered zone, Stage III quartz + pyrite + sphalerite + galena ± chalcopyrite ± green fluorite ± pink calcite in prophylitic altered zone and Stage IV quartz ± calcite vein in carbonatization zone based on cross-relationship. The Stage IIa and IIb veins characterize the main molybdenum mineralization stages. By microthermometry, CO2-bearing (C-), Water (WV- and WL-), and daughter minerals-bearing (S-) types of inclusions were recognized. The Stage I quartz contains C-type fluid inclusion assemblages (FIAs) with a salinity of 6.3 ± 1.4 wt% NaCl equiv., and a total homogenization temperature (Th, total) of 473 ± 3 °C. This suggests that the early fluids show characteristics of high temperature, CO2-rich, and moderate salinity, distinguishing them from those of Endako-type and Climax-type deposits. C-type and coexisting W-type FIAs from Stage IIa show similar salinity, ranging from 1.9 to 13.0 wt% NaCl equiv. and 1.9 to 14.1 wt% NaCl equiv., with Th, total of 349–376 °C and 327–392 °C, respectively. Moreover, C-type FIAs homogenize to distinct phases and also show similar homogenization temperatures, indicating fluid immiscibility. The FIAs in Stage IIb show an average salinity of 8.3 ± 7.4 wt% NaCl equiv. and a Th, total of 302 ± 14 °C. WL-type and WV-type FIAs coexist, with similar temperatures varying from 308 to 310 °C during this stage, indicating significant fluid boiling. These observations indicate that the decrease in temperature, fluid immiscibility, and decompression boiling collectively led to the precipitation of molybdenite. Trapping pressures are estimated to be 82–231 MPa for Stage IIa and 43–115 MPa for Stage IIb, corresponding to ore-forming depths of approximately 8.4 km and 4.3 km, respectively. Additionally, the He-Ar isotopes obtained from pyrite indicate a clear mixing trend of crustal fluids with mantle fluids at Stage IIb, with mantle-derived fluid components increasing during Stage III. This coincides with the tectonic shift from regional compression to extension, leading to the formation of many Dabie-type Mo deposits, alongside crustal thinning and the upwelling of asthenospheric mantle materials. Futhermore, Pb isotopes from the ore, ore-hosted gneiss, and ore-causative granitoids demonstrate that the Taihua Supergroup gneiss supplied ore-forming materials, suggesting a crustal origin for the Leimengou Mo deposit.

Geodynamics and Ore Content of Proterozoic Maphites in the Central Part of the Aldan-Stanovoy Shield (Southern North Asian Craton)

The study of diverse mantle-derived igneous complexes is important for interpreting geodynamic events, ore deposits formation mechanisms, and ore-forming fluid sources. Modern studies of orogenic gold deposits in the Precambrian metamorphosed terranes emphasize the importance of subduction-enriched lithospheric mantle in the ore formation processes. Orogenic gold mineralization in the Nimnyr terrane of the Aldan-Stanovoy shield is confined to the outcrops of mafic granulites from the Medvedev complex, intruded and metamorphosed 1.92–1.90 Ga ago at the final stage of the collision process. The Medvedev complex and ore bodies are intersected by non-metamorphosed dolerites of the 1.87 Ga Timpton-Gynym and 1.75 Ga Timpton-Algamai dike belts formed under conditions of post-collisional and intracontinental extension. The mantle-derived igneous complexes, presenting in a variety of geodynamic settings and ore mineral formation stages, make it possible to identify compositional and evolutionary features of the mantle in connection with ore formation processes. To do this, there were determined rock-forming oxide and trace element concentrations in pre-ore mafic granulites of the Medvedev complex and post-ore dolerites. Based on the geochemical data, there was a reconstruction of rock and mantle source type formation conditions. It was found that the rocks of the Medvedev complex are plume-derived. Doleritic melt formation was contributed to by the subduction-enriched lithospheric mantle material. There is a possility of different degrees of source melting and interaction of plume with the enriched lithospheric mantle at the final stage of the collision process. The obtained results can be used to refine the geodynamic models of gold mineralization formation in the central part of the Aldan-Stanovoy shield. There has been proposed one of the standard models.

The sources and physical–chemical conditions of gold mineralization in the Qi189 porphyry deposit, Qiyugou gold orefield, Eastern Qinling

The Qiyugou gold orefield is situated in the Eastern Qinling. It is a magmatic hydrothermal system, which includes cryptoexplosive breccia-type, vein-type, and porphyry gold deposits. However, the gold sources and physical–chemical conditions of precipitation of the newly discovered porphyry gold deposit, the Qi189, have not yet been well studied. It also hinders the comprehensive understanding of magmatic–hydrothermal gold systems in the Qiyugou gold orefield. Thus, detailed field and microscopic observations, C–O–He–Ar isotopic analysis, in situ major/trace element analysis, and thermodynamic studies on the Qi189 porphyry gold deposit have been carried out in this study. This deposit has three hydrothermal stages: the (I) early quartz–K-feldspar–molybdenite–magnetite stage, (II) middle quartz–sericite–pyrite–Te–Bi-mineral stage, as well as (III) late calcite–quartz stage. The carbon and He–Ar isotopic compositions suggest deep-seated sources of ore-forming fluids with mantle component proportions of up to 37 %. Oxygen isotopic compositions indicate the gradual involvement of more meteoric water in ore-forming fluids during stages I–III. The meteoric water input and reduction in temperature and pressure in the early stage II increased oxygen fugacity and decreased the pH values of ore-forming fluids. Then, in hematite and sulfides formation during late stage II, the oxygen and sulfur fugacities of ore-forming fluids gradually decreased. Precipitation of native gold and Au-bearing telluride grains with quartz-sericite alteration in stage II is significant for Au enrichment, which occurred under acidic (pH = 3.64–5.71), low-logfO2 (<-34.86), low-logfS2 (−13.07 to −11.13) and low-logfTe2 (−15.55 to −10.32) conditions. Therefore, abundant mantle components and changes in the pH, logfO2, logfS2, and logfTe2 of the ore-forming fluids play important roles in gold enrichment. Combined with previous studies, this work also provides some new evidence for identifying a magmatic-hydrothermal gold system in this district, including similar sulfide trace elements, δ13CV-PDB compositions, and changes in logfO2 and logfS2 of various types of gold deposits in a gold orefield.

Fluid source and ore-forming process of the Lishupo Au deposit, NE Hunan: Constraints from fluid inclusions, SIMS oxygen isotope, LA-ICP-MS pyrite trace elements and fsLA-ICP-MS quartz trace elements

The Lishupo Au deposit (4.3 t @ 4.76 g/t) is located in the central Jiangnan Orogen. The processes and origins of regional gold mineralization, as well as the characteristics of the ore-forming fluids, continue to be poorly understood. This study integrates field geology, fluid inclusions, secondary ion mass spectrometry (SIMS) O isotope, femtosecond laser ablation inductively coupled plasma mass spectrometry (fsLA-ICP-MS) trace elements analysis for quartz, and LA-ICP-MS for trace elements study of pyrite to constrain the nature and source of ore-forming fluids, mechanism of gold precipitation, and ore genesis. Field investigations and microscopic observations reveal three mineralization stages at Lishupo: (1) the quartz-pyrite (Qtz1-Py1) stage; (2) the quartz-dolomite-polymetallic sulfides-gold (Qtz2-Py2) stage; and (3) the quartz-carbonate-pyrite (Qtz3-Py3) stage.Cathodoluminescence (CL) observations reveal that Qtz1 and Qtz2 have a homogeneous texture, while Qtz3 exhibits oscillatory zoning. Fluid inclusions in quartz suggest a CO2-H2O-NaCl ± N2 ± CH4 fluid system, which comprise H2O-CO2-NaCl, CO2-rich, and aqueous types. Microthermometry of fluid inclusions indicates low salinity (stage 1: 3.7–7.9 wt% NaCl equiv.; stage 2: 2.2–7.5 wt% NaCl equiv.; stage 3: 1.4–3.9 wt% NaCl equiv.) and medium to low temperature (stage 1: 313–341 °C; stage 2: 209–286 °C; stage 3: 139–198 °C) for ore-forming fluids, consistent with the low Ti content (<10 ppm) found in the quartz. The low Al content (7.99–20.7 ppm) of Qtz1 suggests that the ore-forming fluids were saturated with CO2 and had a near-neutral pH. The Al contents are higher and more variable in Qtz2 (10.7–1959 ppm) and Qtz3 (21.6–713 ppm), which may imply fluctuations in fluid pH. δ18OFluid values for various types of quartz (Qtz1: 9.02–10.95 ‰, Qtz2: 6.30–7.68 ‰, Qtz3: 3.45–3.94 ‰) indicate a metamorphic fluid origin for stages 1 and 2 fluids, which were mixed with the meteoric water during stage 3. The highest concentrations of Au and As in Py2 suggest that the Qtz2-Py2 stage is the primary ore stage. The Co/Ni ratios of all types of pyrite are less than 1, indicating that the ore-forming materials are derived from metamorphic sedimentary rocks. Fluid inclusion microthermometry suggests that fluid immiscibility was responsible for the gold deposition during the Qtz2-Py2 stage. Fluid immiscibility destabilizes Au(HS)2-, leading to the precipitation of native gold. These data strongly suggest that the Lishupo gold deposit is classified as an orogenic-type deposit. Integrating the existing geochronology data and geological context, we emphasize the presence of the Late Triassic orogenic gold deposit in the Jiangnan orogen. This highlights a significant exploration target area within this zone for future gold prospecting.

Mineralogical evidence for the role of deep magmatic fluids in beryllium enrichment in magmatic-hydrothermal systems

Vein-type and greisen-type beryllium (Be) mineralization is closely associated with the magmatic-hydrothermal evolution in highly fractionated granites. However, the source of ore-forming fluids and their role in the migration and enrichment of Be is poorly understood. Although whole rock Ba-Rb isotope researches highlight that even deep magmatic fluids beneath the shallow magmatic-hydrothermal systems could provide rare metals and promote mineralization, it is still challenging to determine the influences of such fluids via using conventional geochemical indicators. Here we present zircon-monazite-xenotime-wolframite U-Pb ages, whole-rock geochemistry, monazite Nd isotopes, as well as muscovite and beryl geochemistry for the Zhujiayingzi quartz vein-type Be mineralization in the southern Great Xing’an Range (SGXR), Northeast (NE) China, and introduce the neighboring Nasigatu gresien-type Be mineralization for comparison. Geochronological results reveal that the Zhujiayingzi beryl-wolframite-bearing quartz veins formed in the Early Cretaceous (149–147 Ma), much younger than the host Permian (270–267 Ma) crystal tuffs, but coeval with the Nasigatu highly fractionated alkali-feldspar granite (144–139 Ma). Similar muscovite-beryl compositions and monazite Nd isotopes, combining with their close temporal-spatial relationships indicate that the Zhujiayingzi and Nasigatu Be mineralization have consistent hydrothermal assemblages and enrichment processes. Higher silica, K, and lower Al contents of muscovites from Be-rich veins (M2) and greisens (M4) than those recorded in barren crystal tuffs (M1) and alkali-feldspar granite samples (M3) at both Zhujiayingzi and Nasigatu are consistent with the evolution of the Early Cretaceous granitic magma, proving the involvement of shallow magmatic fluids exsolved from the Nasigatu-like highly evolved granitic melts. However, ore-related M2 and M4 samples have higher Mg (>1 wt%) and Ti contents than those of M1 and M3 samples, which violates the conventional hydrothermal evolution trend. Trace element compositions as well as K/Rb, K/Cs, and Rb/Sr ratios of four-type muscovites, together with the core-rim geochemical variations of muscovites at Zhujiayingzi and beryls at Nasigatu, indicate the existence of deep magmatic fluids rather than fluid-rock interaction to account for the anomalous mineralogical evidence. Such deep magmatic fluids were exsolved from large silicic magmatic reservoirs beneath the shallow magmatic-hydrothermal system, and thus likely display low evolution degrees and high Mg-Ti contents. They can not only provide heat and promote fluid-mineral interactions, but also can efficiently extract and transport Be enriched in deep crystal mushes at different depths. Thus we invoke that the Early Cretaceous Be mineralization in the SGXR was achieved under the combined action of both shallow and deep magmatic fluids derived from the crystal mush-dominated transcrustal magmatic system.

Biotite chemistry as an indicator of hydrothermal deposit types and fluid sources: Insights from big data compilation, multivariate statistical analysis, and machine learning

Identification of a deposit type in an early stage of exploration can save money and time. However, despite several studies, there is a lack of simple deposit classifiers based exclusively on the major and trace element chemistry of minerals, which is relatively easier to measure. Furthermore, the identification of fluid source is crucial for any ore-genetic study, as it exerts a first order control on physicochemical characteristics of fluid, which ultimately control the alteration mineralogy, metal solubility and mobilization, and metal association in a deposit. The stable isotope composition (e.g., δ34S, δ13C, δ18O, δ11B, etc.) of rocks and minerals is conventionally used to constrain the source of ore-forming fluids, however, the potential of mineral chemistry for constraining fluid source is not well-explored. In this study, we compile the major element composition (wt% of oxides) of a large number (n = 1932) of hydrothermal biotite from various ore settings and execute multivariate statistical analysis and machine learning-based predictive modeling to explore the potential of using biotite chemistry as an indicator of deposit type and fluid sources. The atoms per formula units (i.e., apfu values), and calculated parameters (e.g., Xphl, chlorine intercept value, log(fH2O/fHCl)fluid) is used to perform principle component analysis (PCA) and partial least square discriminant analysis (PLS-DA). The results show that among the different ore settings, iron-oxide copper‑gold, Archean gold, porphyry, and magmatic-hydrothermal rare earth metals deposits and among the fluid sources, (meta-)evaporitic, magmatic-hydrothermal, and metamorphic fluid sources can be reliably discriminated using biotite chemistry. We also show that skarn, hydrothermal platinum group elements, and carbonatite-related rare earth elements deposits may not be discriminated using biotite chemistry. Similarly, mafic rock-derived, carbonatite-derived, and meteoric fluid sources may not be discriminated by biotite chemistry. We propose multiple binary and ternary classifier diagrams, which can be used as discriminator of deposit types and fluid sources. Furthermore, we have developed four different PLS-DA predictive modeling, two for deposit types and two for fluid sources, which can predict deposit types and fluid sources with good accuracy. We provide a Windows© based program that can be used to discriminate deposit types using our PLS-DA predictive modeling. The binary and ternary classifiers and the Windows© programs are tested with recently published biotite data, and it has been shown that these classifiers and programs can efficiently separate deposit types and fluid sources. We also discuss about the limitations of the classifiers.

Computational simulation of the hydrothermal ore-forming system associated with the Luziyuan Pb-Zn Deposit, Yunnan, China: An example of pore-fluid convection controlled mineralization

The giant Luziyuan Pb-Zn deposit is a typical hydrothermal ore-forming deposit in the southern Baoshan block of SE Tibet. Although extensive studies were conducted to understand the ore-forming system associated with the Luziyuan Pb-Zn deposit through using the traditional geoscience methods, the ore-forming process involved in this deposit has not been justified in a strictly scientific manner to date. In this paper, the hydrothermal ore-forming process of the Luziyuan Pb-Zn deposit is computationally simulated through using the dual length-scale approach associated with the finite element method (FEM). In the dual length-scale approach, the FEM is first used to simulate the regional model of a large length-scale in the geological region where the Luziyuan Pb-Zn deposit is located. Afterward, the FEM is then used to simulate the deposit model of the Luziyuan Pb-Zn deposit. Particularly, the boundary conditions of the deposit model are consistently determined from using the computational simulation results of the regional model. The related numerical results demonstrated that: (1) the pore-fluid convection provides a continuous source of ore-forming fluid and ore-forming material for the Luziyuan Pb-Zn deposit; (2) the convective pore-fluid flow is the main dynamic mechanism, which controls the temperature, pore-fluid velocity and chemical species distribution in the Luziyuan Pb-Zn deposit; (3) the localized structure is the main controlling factor for the localized pore-fluid flow pattern, which further controls the formation and location of the orebody in the Luziyuan Pb-Zn deposit; (4) the dual length-scale approach associated with the FEM is very useful for simulating the hydrothermal ore-forming process of the Luziyuan Pb-Zn deposit.

Analysis of the data in Jingwen Mao's paper on the stable isotopes (δDH2O, δ18OH2O, δ 34S) of the gold deposits in Jiaodong Peninsula, China

In 2008, Jingwen Mao published a paper on the stable isotopes of gold deposits in the Jiaodong Peninsula. The paper has a series of problems in obtaining δDH2O and δ18OH2O of ore-forming fluids and interpreting δ34S data. ① In order to obtain δDH2O and δ18OH2O data of ore-forming fluids, Jingwen Mao selected sericite (a total of 25 samples) as the target mineral. Sericite is not an independent mineral and has no fixed molecular formula. New research has shown that it is a fine-grained aggregate composed of muscovite, illite, and sodium mica (at least muscovite and sodium mica). The water content in sericite is very complicated, including structural water, interlayer water, fissure water, primary and secondary inclusion water. Jingwen Mao extracted water from sericite by crushing, and this mixed water cannot represent the ore-forming fluids. It is unreliable to determine the source of ore-forming fluids using δDH2O measured by this kind of mixed water. ② So far, no oxygen isotope fractionation coefficient relationship between sericite and water has been obtained, whether through theoretical calculation or experimental research. In order to calculate the δ18OH2O of ore-forming fluids by measuring the δ18O of sericite, Jingwen Mao used the oxygen isotope fractionation coefficient relationship between muscovite and water for calculation, which is completely wrong. ③ The data of δ18OH2O and δDH2O of ore-forming fluids obtained by Jingwen Mao using sericite are very different from the relevant data obtained by previous researchers using quartz as the target mineral (131 samples). Based on those unreliable data, Jingwen Mao believed that the ore-forming fluids came from the mixed source of crust and mantle, while the relevant data of previous researchers proved that the ore-forming fluids came from the products of atmospheric precipitation exchanging with Jiaodong Group metamorphic rocks under different temperatures and different W/R ratios. ④ For the relationship between the high or low δ 34S value of sulfide minerals and the large or small logfO2 value, Jingwen Mao's explanation is completely opposite to the research results of Ohmoto and Wang. Ohmoto believed that the two were negatively correlated, while Jingwen Mao believed that they were positively correlated. This is a common sense mistake.

Melt extraction and mineralization: A case study from the Shuangjianzishan supergiant Ag-Pb-Zn deposit (208 Mt), Inner Mongolia, NE China

The supergiant Shuangjianzishan (SJZ) Ag-Pb-Zn deposit is in the southern segment of the Great Hinggan Range (SGHR), northeast China. Previous studies suggest the ore-forming material and fluid originated from the magmatic system, and the mineralization age was consistent with the diagenetic age. However, the relationship between granitic magmatism and mineralization is still unclear in the SJZ. In this study, C-H-O-He-Ar and in-situ S-Pb isotope analyses were conducted to determine the sources of ore-forming fluids and metals, which were combined with geochemistry data of SJZ granitoids from previous studies to constrain the relationship between the magmatism and the mineralization. The C-H-O-He-Ar-S-Pb isotopic compositions suggested the SJZ ore-forming material and fluids were derived from a magmatic source, which has mixed a small amount of mantle-derived materials. In addition, the disseminated sulfide from the syenogranite has comparable S-Pb isotopic composition with the sulfide minerals from ore veins, suggesting that the generation of the SJZ ore-forming fluids has a close relationship with the syenogranite magmatism. Combining with the geochemical characters of the syenogranite, the authors proposed that the mantle-derived fingerprint of the SJZ ore-forming fluid might be caused by the parent magma of the syenogranite, which was derived from partial melting of the juvenile lower crust, and underwent the residual melts segregated from a crystal mush in the shallow magma reservoir. The extraction of the syenogranite parent magma further concentrated the fertilized fluids, which was crucial to mineralization of the SJZ Ag-Pb-Zn deposit.©2023 China Geology Editorial Office.

Genesis of the Shaquanzi Zn–Pb deposit in the Eastern Tianshan, NW China: Constraints from geology, fluid inclusion and isotope geochemistry

The Shaquanzi Zn–Pb deposit, located in the Central Tianshan Terrane, is mainly hosted by siliceous slates and carbonaceous marbles of the Mesoproterozoic Kawabulake Group, and its mineralization / alteration can be divided into skarn period (I: early skarn stage, II: late skarn stage), quartz-sulfide period (III: early sulfide stage, IV: late sulfide stage and V: quartz-calcite stage) and supergene period (VI: supergene alteration stage). The W-type fluid inclusions (FIs) were identified in the garnet, chlorite, quartz, and calcite in skarn and quartz-sulfide periods. Detailed fluid inclusion study shows temperature of fluids decreased from Stage I (510–520 °C) through, Stage III (481–507 °C), Stage IV (248–417 °C, peak at 280–400 °C) to Stage V (148–260 °C, peak at 200–220 °C), with salinities of 20.8–22.2 wt% NaCl eqv., 19.8–29.1 wt% NaCl eqv., 10.6–27.8 wt% NaCl eqv. (peaks at 20–23 wt%), and 21.6–29.9 wt% NaCl eqv. (peak at 23–27 wt%), respectively, indicating that the ore-forming fluids consisted of a high-medium salinity and Na-Mg-Fe-Ca-rich fluid system, and may have evolved from high-medium temperature to medium temperature. The H–O isotopic compositions varied from Stage III (δ18OH2O = 7.7 ‰–9.0 ‰ and δDH2O = − 105 ‰ to − 91 ‰) through Stage IV (δ18OH2O = 2.6 ‰ to 4.3 ‰ and δDH2O = − 114 ‰ to − 111 ‰) to Stage V (δ18OH2O = − 4.2 ‰ to − 3.7 ‰ and δDH2O = − 119 ‰ to − 96 ‰), suggesting that the ore-forming fluid sources may have evolved from magmatic fluids to meteoric water. The average δ34SH2O values of the early sulfide, late sulfide, and quartz-calcite stages are 5.7 ‰, 8.5 ‰ and 14.0 ‰, respectively, indicating that the sulfur in the early stage was mainly derived from magmatic hydrothermal sulfur, while the increase of the δ34SH2O values in the late stages is likely to be sourced from the Kawabulake Group through water–rock reaction. Above all, we propose that the Shaquanzi may have been a skarn-type Zn–Pb deposit.

In situ trace elements and sulfur isotope analyses of layered sphalerite as a record of ore-forming processes in the world-class Jinding sediment-hosted Zn-Pb Ore Deposit, China

The Jinding deposit is well-known to contain high concentrations of metals Zn, Pb, Cd, Tl, Ag, etc. in the world. The associated critical metals and their substitution mechanisms were wildly concerned. This study investigated and compared sphalerites using a combination of textural, trace element, and sulfur isotopic analyses to give insights into element substitution mechanisms and possible sources of ore-forming fluids and to constrain processes involved in ore genesis of the world-class Jinding sediment-hosted Zn-Pb deposit. LA-ICP-MS analyses reveal chemical zoning in the sphalerites together with the coupling of two main groups of trace elements substitution mechanisms: one is Fe + Ge + Mn + Pb + As + Tl and vacancies to substitute Zn, and the other is Cd + Cu + Ag + Sb to substitute Zn. The incorporation of trace elements is facilitated by the replacement of Zn by Cd and Fe. These two group elements have distinct color oscillatory zonation and are intertwined in the trace element LA-ICP-MS element maps. The sulfur isotopic values show high isotope fractionation in the sphalerite from −28.4 to −0.5 ‰, suggesting a bacteriogenic sulfur origin at Jinding. Sphalerite sample has observed that sulfur isotope is correlated with Fe concentration and anti-correlated with Cd concentration. These variations in isotope fractionation and trace element disequilibrium partitioning were interpreted as the effects of temperature and pH with less influence from sulfur activity. These variability zones of sphalerite alternately enriched in Cd- and Fe-related elements suggested that ore fluids may flow from metal-fertile sedimentary/basement sequences during their ascent, and colloform sphalerite was likely formed by a high degree of supercooling, over-saturation, and rapid mixing between bacteriogenic sulfur and metal-rich in spaces of collapse dome. Based on our observations, we suggested that these variability zones of layered sphalerite alternately enriched in Cd and Fe would likely provide useful insight for a potential economic Zn-Pb and associated critical metals mineral exploration deposit.

Fluid provenance and genetic type of the Bubin Cu-Pb polymetallic deposit, Kohistan-Ladakh island arc, north Pakistan: Evidence from mineralogy, fluid inclusion and O-H-S-Pb isotopes

The Bubin Cu-Pb polymetallic deposit in Gilgit-Baltistan, Pakistan, is a well-known vein-type ore deposit located in the Kohitan-Ladakh island arc. Due to its significant economic importance as the most important deposit type in the Kohistan-Ladakh island arc, a comprehensive study on its ore genesis, fluids evolution, and genetic classification not only shed new light on our understanding the formation of such polymetallic deposit at a typical intra-oceanic arc, but also of help for the mineral exploration. Here, we present the results from electron probe micro-analyzer, fluid inclusions, Raman spectroscopy, and isotopic studies (O-H-S-Pb) to gain insights into the source of ore-forming fluids and materials, as well as the genetic-type and mechanism of ore precipitation for the Bubin deposit. The mineralization processes were divided into three main stages: Stage I (quartz-pyrite), Stage II (quartz-sulfide), and Stage III (quartz-carbonate). Stage II further comprised two sub-stages: IIa (quartz-chalcopyrite-magnetite) and IIb (quartz-galena-fahlore). The ore-forming fluids exhibited high to moderate temperatures (154–540 °C) and varying salinities (0.35–44.30 wt% NaCl) throughout the stages. Stage I fluids displayed critical behavior with high temperature and low salinity, and their isotopic signatures suggested a magmatic origin. Subsequently, the ore-forming fluids gradually evolved from primary magmatic origin to the mixing of meteoric water, as demonstrated by oxygen and hydrogen isotopic values (δ18Ofluid = -1.34 to 6.29 ‰, δD = -112.4 to −76.1 ‰). The δ34S values (-2.92 to 6.52 ‰) and Pb isotopic ratios (208Pb/204Pb = 39.06 to 40.93, 207Pb/204Pb = 15.72 to 15.99, and 206Pb/204Pb = 19.44 to 20.80) suggested a deep magmatic source for the ore-forming fluid, with metals primarily derived from the upper crust, likely associated with the Ladakh Batholith. Fluid boiling and maxing are the dominant mechanisms for ore mineral precipitation. Additionally, the high to moderate temperature and salinity, presence of solid-bearing and vapor rich inclusions, a Co/Ni ratio > 1, the Ni-As-Co diagram, and O-H-S-Pb isotopic evidence collectively support the classification of the Bubin Cu-Pb polymetallic deposit as an intrusion-related porphyry-style magmatic hydrothermal deposit.

Genesis of the Daliuhang Gold Deposit, Jiaodong Peninsula, Eastern China: Constraints from H-O-S-Pb-He-Ar Isotopes, and Geochronology

The Daliuhang gold deposit in the Qipengfu (Qixia–Penglai–Fushan) ore concentration area is a typical gold deposit of medium-low temperature hydrothermal veins. Uncertainties regarding the primary sources of ore-forming fluids, as well as whether host rocks contribute materials to the mineralization of the gold deposits in the Jiaodong Peninsula, are still subject to intense debate. Hydrogen–oxygen isotope results show that atmospheric water is involved in ore-forming fluids. According to the results of the helium–argon isotopes of pyrite, it is hypothesized that the initial fluid source was located in the oceanic crust or upper mantle lithosphere above the Early Cretaceous Paleo-Pacific Plate, as it was subducted into the eastern part of the eastern North China Craton. In situ sulfur isotope results show that high δ34S values characterize the pyrite in the main mineralization period. It is inferred that during the thinning and melting process of the lithospheric mantle, the volatile components enriched in pyrite contributed to the release of δ34S. At the same time, when the fluids ascended to the weak zones, such as fissures of ore-endowed peripheral rocks, the δ34S in the peripheral rocks were extracted, and the two processes acted together to cause high δ34S values to occur. Similarly, the lead and strontium isotopic compositions indicate a crust–mantle mixing attribute of the mineralized material source. The zircon U–Pb age of the ore-hosting granodiorite was 130.35 ± 0.55 Ma, and the Rb–Sr isochron age of the pyrite from the main mineralization period was 117.60 ± 0.10 Ma, which represents the timing of felsic magmatism and gold mineralization, respectively, with at least 10 Ma between the magmatism and mineralization. The magma gradually cooled over time after its formation, and when the granodiorite cooled down to 300 ± 50 °C, the temperature and pressure conditions were most conducive to the precipitation of gold. It is inferred that gold-rich initial mantle fluids with volatile components, rising along tectonically weak zones, such as fractures, underwent fluid phase separation in the fractured position of the granite and extracted the gold from the granodiorite, forming gold deposits.

The origin and evolution of the ore-forming fluids at the Manondo-Choma gold prospect, Kirk range, southern Malawi

Abstract This study provides an in-depth analysis of fluid inclusions (FIs) and stable isotopes from the Manondo-Choma gold prospect in southern Malawi to understand the ore-forming mechanisms, genesis, and evolution of the hydrothermal fluids responsible for gold mineralization at the Manondo-Choma gold prospect. FIs and microthermometry studies were carried out on mineralized quartz veins from the area. The Manondo-Choma gold prospect is located in the southern Malawi within the Kirk range. Gold is mostly found in quartz veins within metamorphic rocks, such as gneiss and schists, and is structurally controlled by the NE–SW ductile shear zones. Gold mineralization is linked to quartz sulfide veins. Mineralization occurs in the following three stages: early, middle, and late, of which the middle stage is more plorific. The following three FI types were recognized in the quartz veins: pure carbonic, aqueous carbonic (CO2–H2O) and aqueous (H2O–NaCl) inclusions. Gold and associated mineralization were likely precipitated due to the lowering of pressure and fluid immiscibility. Oxygen isotope data indicate that the source of ore-forming fluids at the Manondo-Choma gold prospect was largely metamorphic in origin with minor magmatic input.

Geochronology and ore-forming fluid source of the Buzhu orogenic gold deposit in southern Tibet

The Buzhu gold deposit is a newly discovered and representative gold deposit in the Indus-Yarlung Zangbo suture zone. At Buzhu, auriferous quartz veins with paragenetic sequences of quartz-pyrite-sericite hosted by Early Jurassic greenschist facies rocks, and gold occurs mainly as invisible lattice gold in pyrite as well as minor as visible micrograins inside (arseno)pyrite fractures. We have recognized two auriferous pyrite generations formed in the syn-ore stage (Py2a and Py2b). Py2a is euhedral-subhedral granular with cavities, whilst Py2b mainly grew colloidally around Py2a, indicating that pre-existing pyrite may have been dissolved to form the porous Py2a and Py2b rim. Py2a and Py2b have similar δ34SV-CDT values of 6.98‰ to 7.54‰ and 6.18‰ to 6.85‰, respectively, which are also similar to those of the ore-hosting sediments (6.08‰ to 7.08‰). In-situ trace element analysis shows that Py2b (avg. 1.63% Au) contains more gold than Py2a (avg. 0.42% Au). Combined with petrological and geochemical data, we hypothesized that the gold was derived from the metamorphic devolatilization of the sedimentary wallrocks, and pyrite dissolution-reprecipitation has driven the gold enrichment from Py2a to Py2b. The sericite Ar-Ar date of 19.60 ± 0.66 Ma likely represents the gold mineralization age, as the dated sericite coexists with the auriferous pyrite. This age is much younger than most orogenic gold mineralization (ca. 60–41 Ma) in southern Tibet and indicates an orogenic gold mineralization event (ca. 20–15 Ma) related to extensional tectonics during the late-stage India-Asia continental collision.

Mineralization process of the Mazhala Au–Sb deposit, South Tibet: Constraints from fluid inclusions, H-O-S isotopes, and trace elements

The Mazhala deposit is a typical Au-Sb deposit in the northern Himalayan orogenic belt that has increasingly attracted worldwide attentions. However, debates remain regarding the source of ore–forming fluid and its evolutionary process. Herein, we investigate the genetic and compositional evolutionary characteristics of different types of pyrite grains in order to better constrain the ore–forming fluid source and ore–forming processes by means of Using in-situ trace and sulfur isotope data of pyrite and inclusion temperature and H-O isotope data of quartz. Based on the occurrence and morphological features of pyrite, four types of pyrite (Py0, Py1, Py2, and Py3) have been identified. The framboids of pyrite Py0 have high contents of Au, Ag, Cu, Pb, and Sb, with Co/Ni < l, and their δ34S values range from −34.0‰ to −19.3‰, indicating a sedimentary-diagenetic origin. Py1 pyrite exhibits stark core-rim structure. The contents of Sn, Ti, Be and W in Py1c are higher, with Co/Ni > 1. The δ34S of Py1c ranges from 0.30 to 3.9‰ (mean = 1.7‰), indicating a magmatic hydrothermal transformation origin. Py1r, Py2, and Py3 differ greatly in pyrite morphology and trace element contents, with Co/Ni < 1, indicating as hydrothermal sedimentary transformation origin. The δ34S values of Py1r, Py2, and Py3 vary from 1.4 to 6.50‰, interpreted as the presence of metamorphic sulfur sources. The δ34S values of Py1-Py2-Py3 firstly increases and then decreases, indicatinga fluid mixing process. The Mazhala ore–forming fluid is typical of low temperature (270–291 °C), low salinity (1.1–5.0 wt%NaCl equiv) and CO2-enrichment, with H-O isotopic compositions of quartz resembling magmatic and/or metamorphic water, which makes us to infer a mixture of magmatic and/or metamorphic water source for the Mazhala ore-forming fluid. The early pyrite grains were dissolved and reprecipitated under the action of fluid. In the process of multistage hydrothermal interaction, Au and other trace elements were released from the primary pyrite lattice into the fluid, forming the gold–bearing ore–forming fluid. Separation of fluid phase coupled with significant change in the pH value of fluid prompted the co-precipitation of Au and Sb to form the Mazhala Au-Sb deposit.

Discovery of the large-scale Eocene Xiwu Pb–Zn–Ag deposit in the Tethyan Himalaya: Geochronology, geochemistry, and C–H–O–S–Pb–Sr–Nd isotopes

The known Pb–Zn–Sb–Au polymetallic deposits in the Himalaya mainly formed during the main-collisional convergence (65–41 Ma) and post-collisional crustal extension (25–0 Ma) tectonic settings. Here, we report the discovery and genesis of the large-scale Eocene Xiwu Pb–Zn–Ag deposit that formed during the late-collisional tectonic transition stage (40–26 Ma) in the eastern Himalaya. The surrounding ore-hosting rocks are mainly low-grade metamorphosed Jurassic clastic rocks and Early Cretaceous diabase. The most important ore-controlling structures are NE–SW thrust faults. The ore minerals include large amounts of galena, sphalerite, tetrahedrite and siderite, with minor chalcopyrite, pyrite, arsenopyrite, calcite and quartz. In this contribution, we analyzed the S–Pb isotopes of sulfides, fluid inclusions and the C–H–O–Pb–Sr–Nd isotopes of nonmetallic minerals. The results indicate that the ore-forming materials originated from deeper metamorphic rocks of the Greater Himalayan Crystalline Complex. This study infer that the source of ore-forming fluids was mainly metamorphic fluids with moderate temperatures and salinities, and S and C were mainly derived from microbial sulfate reduction and the decarboxylation of organic matter, respectively. The main ore-forming mechanism is fluid mixing between the deep ore-bearing metamorphic fluids and shallow formation waters. The Sm–Nd isotopic age of siderite is 37.4 ± 1.1 Ma, which is slightly younger than the zircon U–Pb age of the Zhunba leucogranite (38.9 ± 0.4 Ma) but is consistent with the main epoch of early prograde metamorphism (43–36 Ma) in the Himalaya. We propose a new metallogenic model for Himalayan Pb–Zn–Ag deposits that can greatly promote ore prospecting. The genetic type of the Xiwu deposit is a clastic-dominated subtype of sediment-hosted Pb–Zn deposits.

Fluid evolution and metallogenesis of the Zhangjiapingzi gold deposit in mianning, Sichuan province: constraints from fluid inclusion studies

Introduction: The Zhangjiapingzi gold deposit, located at the western margin of the Yangtze Craton and controlled by the Jinhe-Chenghai deep fault, is a newly discovered super-large gold deposit in the Danba-Mianning metallogenic belt. The gold ore bodies are hosted in the Middle Triassic (T2) altered dolomite (Dm), and have two types of mineralization: altered rock type and quartz vein type. Previous studies on this deposit are rare, especially on the ore-fluid characteristics, which limit the understanding on the ore genesis.Methods: This study focused on fluid inclusions in quartz from altered rocks, and used microthermometry and laser Raman spectroscopy to investigate the properties and sources of ore-forming fluids, and to determine the ore genetic type.Results and discussion: The results show that the fluid inclusions are mainly CO2-H2O-NaCl inclusions, with medium temperature (220–300°C), low salinity (&amp;lt;10%), medium-low density (0.79–1.01 g/cm3) and high contents of CO2 and CH4, resembling typical orogenic gold ore fluids. We suggest that the Zhangjiapingzi is best classified as orogenic type, and our findings provide new insights into the fluid origin and metallogenesis of orogenic gold deposits in the Danba-Mianning metallogenic belt.