NaCl Equiv Research Articles

Fluid evolution of the Nulasai Cu deposit, Xinjiang, NW China: Evidence from fluid inclusions and O-H-C isotopes

The Nulasai deposit is the earliest Cu mine in Xinjiang, NW China, and has been mined and smelted since the warring state period. Another striking characteristic of the deposit is the high-grade (ave. 1.34 % Cu) with bornite, chalcopyrite and chalcocite as main ore minerals. Through a field and petrographic investigation, three phases of hydrothermal evolution have been recognized at the Nulasai Cu deposit, including the stage I magnetite – quartz ± chalcopyrite ± bornite veins, the stage II calcite – barite ± chalcopyrite ± chalcocite ± pyrite ± bornite veins, and the stage III calcite – barite ± chalcopyrite ± sphalerite ± pyrite ± galena veins. Fluid inclusions of the stage I veins were captured under two-phase condition indicates that existence of both contemporaneous daughter mineral-bearing and liquid-rich fluid inclusions; they have an intermediate-high salinity (11.5 ∼ 38.5 wt% NaCl equiv) and homogenization temperature (266 ∼ 376 °C), with entrapment pressures from 47 to 167 bar (depth of approximately 0.5 to 1.7 km). The coexistence of vapor-rich and liquid-rich fluid inclusions was a defining feature of the stage II fluid inclusions, and they have an intermediate salinity (6.2 ∼ 10.7 wt.%NaCl equiv) and homogenization temperature (211 ∼ 287 °C), with entrapment pressures from 18 to 70 bar (depth of approximately 0.2 to 0.7 km). Fluid inclusions of the stage III veins were captured under two-phase condition, and intermediate-low salinity (3.2 ∼ 9.2 wt.%NaCl equiv) and homogenization temperature (155 ∼ 241 °C), with entrapment pressures of 6 to 32 bar (depth of 0.1 to 0.6 km). According to the stable isotope (O-H-C) data for the three mineralization phases, magmatic water containing organic carbon made up the majority of the early ore-forming fluids, whereas abundant meteoric water has been involved during the late stage of mineralization. Therefore, we suggest that fluid mixture between magmatic water and meteoric water may have led to simultaneous decrease of fluid temperature, salinity and their stable isotope values, and finally facilitates the Cu ore precipitation. This study emphasizes how high-grade Cu deposition in orogenic belts is initiated by fluid dilution.

Genesis of the Jianbeigou Gold Deposit on the Southern Margin of the North China Craton: Insights from Fluid Inclusions, H‐O‐S Isotopes, and Pyrite in situ Trace Element Analyses

AbstractThe Jianbeigou gold deposit is a typical lode gold deposit in the Qinling metallogenic belt, located on the southern margin of the North China Craton. Three stages of the hydrothermal process can be distinguished, including the quartz ± pyrite, quartz‐polymetallic sulfide, and quartz‐carbonate ± pyrite stages. From the early to late stages, the homogenization temperatures of primary fluid inclusions are 281–362°C, 227–331°C, and 149–261°C, respectively. The corresponding salinities estimated for these fluids are 3.9–9.9 wt%, 0.4–9.4 wt%, and 0.7–7.2 wt% NaCl equiv. Combined with laser Raman spectroscopy data, the ore‐forming fluid belongs to a H2O‐CO2‐NaCl ± CH4 system with medium–low temperature and salinity. The δ18Ofluid and δD values for the quartz veins are –1.0‰ to 6.0‰ and –105‰ to –84‰, respectively, which indicates that the ore‐forming fluid is of mixed source, mainly derived from magma, with a contribution from meteoric water. Pyrite has been identified into three generations based on mineral paragenetic sequencing, including Py1, Py2, and Py3. The pyrites have δ34S sulfur isotopic compositions from three stages between 3.7‰ and 8.4‰, indicating that sulfur mainly originated from magma. Te, Bi, Sb, and Cu contents in pyrite were all high and showed a strong correlation with Au concentrations. Native gold and the Au‐Ag‐Bi telluride minerals were formed concurrently, and the As concentration was low and decoupled from the Au content. Therefore, Te, Bi, Sb and other low‐melting point chalcophile elements play an important role for gold mineralization in arsenic‐deficient ore‐forming fluid. Combined with the geological setting, evolution of pyrite, and ore‐fluids geochemistry, we propose that the Jianbeigou deposit can be classified as a magmatic–hydrothermal lode gold deposit. Gold mineralization on the southern margin of the North China Craton is related to Early Cretaceous magmatism and formed in an extensional setting.

The Geology, Fluid Inclusions, and O‐S Isotopes of the Mibei Gold Deposit, Hunan Province, Southern China

AbstractThe Mibei gold deposit, located in the southwestern part of the Xuefengshan uplift zone, the middle section of the Jiangnan orogenic belt in southern China, has estimated gold resources of approximately seven tons. This deposit is primarily a quartz vein‐type gold deposit, with ore bodies occurring mainly within Neoproterozoic metasediments. The main metallic minerals in the ore are pyrite, chalcopyrite, and arsenopyrite. In this study, the petrography and microthermometry of ore‐forming fluid inclusions, oxygen isotopes of gold‐bearing quartz, and sulfur isotopes of gold‐bearing sulfides and arsenopyrite were analyzed. Three types of fluid inclusions were identified: type Ia three‐phase inclusions comprising vapor and two phases of liquids (VCO2 + LCO2 + LH2O), type Ib two‐phase liquids (LCO2 + LH2O), type II two‐phase vapor‐rich inclusions (V/V + L > 50%), and type III pure liquid inclusions. Type I inclusions were heated uniformly to the liquid phase, type II inclusions were heated uniformly to the gas phase, and type III inclusions were heated without change. In general, the temperature range of homogenization to liquid phase of fluid inclusions in the Mibei gold deposit is 204–227°C. The salinity of the inclusion ranges from 4.6 to 12.2 wt% NaCl equiv. The δ 18OSMOW of gold‐bearing quartz varies from 16.9‰ to 17.5‰. The δ 18OH2O of gold‐bearing quartz are varied from 6.5‰ to 7.5‰. The δ34S values of gold‐bearing pyrite range from 1.7‰ to 6.8‰. The δ34S values of gold‐bearing arsenopyrite range from 5.6‰ to 5.9‰. The δ34S values of pyrite from wall rocks slate range from 6.4‰ to 11.6‰. This evidence implies that the ore‐forming fluids of the Mibei gold deposit originated from magmatic‐hydrothermal processes, mixing with minor S from the surrounding metasediments. Combined with the evolution of the Jiangnan orogenic belt, due to the magmatic and tectonic activities of the Xuefengshan uplift during the Caledonian period, the fault seal mechanism controlled the ore‐forming process. Overall, the Mibei gold deposit is more akin to a magmatic‐hydrothermal gold deposit.

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.

Mineralogical and ore-fluid characteristics of the Onto Porphyry-HSE transition in Hu’u district, West Nusa Tenggara, Indonesia

Abstract Onto prospect is located in the eastern part of Sumbawa Island in West Nusa Tenggara Province, Indonesia. The island is situated within the Sunda-Banda magmatic arc, which extends from west to east, consists of volcanic rocks from the early Miocene to the Holocene. Onto is one of the highly potential prospects and holds significant economic value among ore deposits in Indonesia. The aim of this research is to explain the geological setting and determine the genesis of mineralization based on petrographic, ore microscopic, and fluid inclusion analyses. Eight lithological units have been identified, namely early andesites, polymictic diatreme breccia, upper sedimentary package, caping andesite, quartz-phyric andesite sill, early porphyry, early intra-mineral porphyry, and late intra-mineral porphyry. Nine samples were analyzed for petrography to identify the alteration types consisting of illite-smectite, quartz-dickite, residual vuggy quartz, silicic, quartz-alunite, quartz-pyrophyllite±diaspore, potassic, phyllic-chloritic, and propylitic alterations. Additionally, pyrite, chalcopyrite, and covellite are predominantly present in the study area. Meanwhile, native gold is found as an inclusion in covellite and pyrite. From micro thermometric analysis of fluid inclusions in quartz veins associated with multiphase intrusive rocks, it is shown that the homogenization temperature of early porphyry ranges on average from 279°C to 377°C, early inter-mineral porphyry ranges from 263°C to 361°C, and late intra-mineral porphyry ranges from 275°C to 336°C. The salinity level of the measurements ranges from 5.71 to 10.27% by weight NaCl equivalent, with an average of approximately 8.15% by weight NaCl equivalent. The mineralization formation during the early or prograde phase is associated with the EDM vein system with a mineralization set of biotite-magnetite, digenite, chalcocite, and coevellite, type A veins with quartz-sulfides + anhydrite, M veins type associated with quartz-magnetite-chalcopyrite-bornite mineralization, AB veins type associated with quartz-sulfides + anhydrite textures, and B veins type with sulfide centerline characteristics. The mineralization system during the early stage is generally associated with potassic alteration (K-feldspar-magnetite-secondary biotite). Whereas the retrograde phase, the vein system is associated C veins type with sulfide mineralization groups consisting of massive chalcopyrite + quartz with phyllic alteration (quartz-muscovite-chlorite ± dickite), D veins type with quartz-pyrite+chalcopyrite associated with advanced argillic alteration (quartz-alunite-pyrophyllite ± diasporite), E veins representing the epithermal stage associated with minerals such as quartz-carbonates, galena, sphalerite, chalcopyrite, tetrahedrite-tennatite in the alteration stage of kaolinite-illite-smektite-sericite.

The Spatial and Temporal Evolution of the Sadisdorf Li-Sn-(W-Cu) Magmatic-Hydrothermal Greisen and Vein System, Eastern Erzgebirge, Germany

Abstract The Sadisdorf Li-Sn-(W-Cu) prospect in eastern Germany is characterized by vein- and greisen-style mineralization hosted in and around a small granite stock that intruded into a shallow crustal environment. The nature and origin of this mineral system are evaluated in this contribution by a combination of petrography and fluid inclusion studies, complemented by Raman spectroscopy and whole-rock geochemical analyses. The early magmatic-hydrothermal evolution is characterized by a single-phase low-salinity (7.0 ± 4 wt % NaCl equiv), high-temperature (>340°C), CO2-CH4–bearing aqueous fluid, which caused greisen alteration and mineralization within the apical portions of the microgranite porphyry. The bimodal distribution of brine and vapor fluid inclusions, and the formation of a magmatic-hydrothermal breccia associated with the proximal vein mineralization are interpreted to mark the transition from lithostatic to hydrostatic pressure. The vein- and stockwork-style mineralization (main stage) displays lateral zonation, with quartz-cassiterite-wolframite-molybdenite mineral assemblages grading outward into base-metal sulfide-dominated assemblages with increasing distance from the intrusion. Late fluorite-bearing veinlets represent the waning stage in the evolution of the mineral system. The similarity in the homogenization temperature (250°–418°C) of fluid inclusions in quartz, cassiterite, and sphalerite across the Sadisdorf deposit suggests that cooling was not a significant factor in the mineral zonation. Instead, fluid-rock interaction along the fluid path is considered to have controlled this zonation. In contrast to quartz-, cassiterite- and sphalerite-hosted fluid inclusions, which have a salinity of 0.0 to 10.0 wt % NaCl equiv, the fluid inclusions in late fluorite veins that overprint all previous assemblages have a salinity of 0.0 to 3.0 wt % NaCl equiv and homogenize at temperatures of 120° to 270°C, thus indicating cooling with or without admixture of meteoric fluids during the waning stage of the mineral system. The Sadisdorf deposit shares similar characteristics with other deposits in the Erzgebirge region, including a shallow level of emplacement, similar mineralization/alteration styles, and a hydrothermal evolution that includes early-boiling, fluid-rock interaction, and late cooling. In contrast to most systems in the region, both proximal and distal mineralization are well preserved at Sadisdorf. The recognition of such spatial zoning may be a useful criterion for targeting greisen-related Li and Sn resources.

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.

Genesis of the Hajibolagh-Zalibolagh Cu-(Ag) intermediate-sulfidation epithermal deposit, Urumieh-Dokhtar magmatic arc, Iran: Evidence from ore geology, fluid inclusions, and stable isotopes

The Hajibolagh-Zalibolagh deposit located northeast of the city of Saveh in the central part of the Urumieh-Dokhtar magmatic arc of Iran, demonstrates vein and breccia vein style copper-(silver) mineralization hosted by Eocene volcano-sedimentary rocks. The main mineralization stage can be divided into four phases, respectively (1) jasperoid + quartz veins, chalcopyrite, and pyrite; (2) quartz veins along with chalcopyrite, bornite, chalcocite, arsenopyrite, and pyrite; (3) quartz-barite veins along with chalcopyrite, bornite, chalcocite and pyrite; and (4) veins of quartz, calcite, hematite, and oligist along with a small number of copper sulfides. The main stages of mineralization are cut by barren post-ore quartz and calcite veinlets. As a result of supergene processes, minerals are oxidized, and malachite, azurite, chrysocolla, chalcocite, covellite, goethite, and hematite are formed, presenting an important exploration guide. The hydrothermal alteration from the center of the vein-veinlets to the outside includes, respectively, silicification, sericitization, intermediate argillic, and propylitic. The average salinity and homogenization temperature (Th) of fluid inclusions is 14.2 wt% NaCl equiv. and 288 °C, respectively. The coexistence of the vapor phase, liquid-rich phase, and halite-bearing fluid inclusions is a sign of boiling in this hydrothermal system, which has contributed to copper saturation. Sulfur isotope values for pyrite, chalcopyrite, chalcocite, and bornite are mainly from –0.16 to 2.98 ‰, indicating a probable magmatic source for sulfur. Boiling, dilution, and mixing are the mechanisms for the ore deposition and facilitated the mineralization. The Hajibolagh-Zalibolagh deposit shows the highest similarity to intermediate-sulfidation epithermal deposits. The best environment for the mineralization and fluid circulation in these epithermal deposits is the intersection of faults with the Eocene volcanic and volcano-sedimentary rocks.

Improvements in the Quantification of End-Member Vapor Compositions in Fluid Inclusion Boiling Assemblages and Implications for Metal Transport by Low-Density Fluids

Abstract Under conditions typically found in the Earth’s crust, there is a large pressure-temperature-composition range in the H2O-NaCl system where fluids may separate into a low-salinity vapor end member and a high-salinity liquid end member. However, heterogeneous trapping is common during the formation of fluid inclusions in an immiscible fluid system, violating the fundamental assumption of homogeneous entrapment for fluid inclusion microthermometry. This has profound consequences on the composition of these fluid phases and consequently on the formation of ore deposits from hydrothermal systems. At the same time, minor mixture of the high-salinity liquid phase with the low-salinity vapor phase cannot be distinguished from the end-member vapor-rich fluid inclusions by their bubble sizes. Precise determination of the salinities of vapor-rich fluid inclusions using microthermometry is deterred by the very small proportion of the liquid phase and the limitation of the analytical precision. All this will lead to erroneous compositional data from fluid inclusion analysis. We have quantitively calculated the variations of fluid inclusion properties caused by heterogeneous entrapment during phase separation in the H2O-NaCl system and showed that the salinity, and thereby the element contents and element/Na ratios of the vapor-rich fluid inclusions, is significantly changed in heterogeneously trapped fluid inclusions. The addition of 1 vol % of the high-salinity end member to the low-salinity end member results in a salinity change from 0.99 to 4.4 wt % NaCl equiv at the phase separation condition of 800 bar and 750°C. This will have a significant impact when it comes to determining the concentration of elements transported as chlorine complexes and typically leads to an overestimation of the mass transport capability by the vapor phase. Therefore, every effort should be taken during microthermometry to find and measure the least affected vapor-rich fluid inclusions. Our numerical calculations and synthetic fluid inclusions reveal that there is a linear relationship between the salinity and element contents for fluid inclusions at different extents of heterogeneous entrapment. Therefore, linear correction to the measured lowest vapor salinity can obtain a good approximation of the element contents in the end-member vapor phase.

Reconstructing fluid evolution and precipitation mechanism of the Chuankeng skarn copper deposits, China: New insight from microthermometry and LA-ICP-MS analysis of fluid inclusions

Skarn deposits are significant sources of copper, yet there are different understandings on their fluid evolution and precipitation mechanism due to lack of direct constraints on fluid compositions of mineralization process. Here, we present a detailed reconstruction of fluid evolution history from the pre-ore prograde stage through the syn-ore retrograde stage to the post-ore stage of the Chuankeng deposit in the North Wuyi area, South China, based on fluid inclusion microthermometry and LA-ICP-MS analysis of typical minerals from three stages. The pre-ore fluids trapped in pyroxene have higher homogenization temperatures (450–550 ℃), higher salinities (31.9–51.5 wt% NaCl equiv), but lower concentrations of Cu (∼556 ppm) than syn-ore fluids (338–465 ℃, 31.3–38.9 wt% NaCl equiv, ∼3247 ppm Cu). The post-ore fluids show lower temperatures (139-163℃), salinities (1.1–6.5 wt% NaCl equiv), and low concentrations of Cu (<387 ppm). Fluids of all paragenetic stages have high K/Na and Rb/Na ratios, exhibiting signatures of magmatic hydrothermal fluids. Mixing of the magmatic fluids with meteoric waters of lower temperature and salinity occurred at the final post-ore stage, thus it is not related to Cu mineralization. As the temperature descends from 445 ℃ to 340 ℃, the Cu/(Na + K) ratios of syn-ore fluids diminish exponentially, manifesting fluid cooling within a certain temperature may be an important factor controlling Cu mineralization. Concomitantly, a moderate negative correlation between the Ca/(Na + K) ratios and Cu/(Na + K) ratios of syn-ore fluids suggests that fluid-rock interaction do have some impact on copper contents. Additionally, the Cu/(Na + K) ratios of syn-ore fluids in quartz are an order of magnitude higher than those of pre-ore fluids, and it is proposed that during the initial retrograde stage—the onset of mineralization—the magma chamber released fluid pulse with higher copper contents. Based on these findings, the fluids of pre-ore prograde stage and syn-ore retrograde stage are distinct magmatic fluid pulses, and copper-rich fluids, thermal cooling within a specific temperature range and fluid-rock reaction are suggested to be key factors controlling metal enrichment in skarn copper systems.

Genesis of the Mahour Base Metal Deposit, Iran: Constraints from Fluid Inclusions and Sulfur Isotopes

The Mahour base metal deposit is located northeast of Badroud in the middle of the Urumieh–Dokhtar magmatic arc in the Isfahan province of Iran. The main host rocks to the ores are Eocene volcanic and volcaniclastic rocks. Hypogene ore minerals constituting the main ore body are galena, sphalerite, pyrite, and chalcopyrite. In addition to gangue quartz, a variety of supergene minerals comprising gypsum, goethite, hematite, “limonite”, malachite, azurite, covellite, and chalcocite are also present; gangue minerals are quartz, barite, calcite, sericite, and chlorite. Silicification, intermediate argillic, and propylitic are the main wall-rock alteration types. The presence of fluid inclusions with different vapor/liquid ratios in quartz and sphalerite could indicate a boiling process. The primary liquid-rich fluid inclusions suggest that the homogenization temperature was between 107 and 298 °C from fluids with salinities from 1.5 to 13.7 wt.% NaCl equiv. These data suggest that the ore-forming fluids were magmatic with a contribution from meteoric waters. The δ34S values of sulfides range from 1.9 to 3.4‰, those of barite range from 12.1 to 13.2‰, and those of gypsum range from 4.3 to 5.6‰. These data suggest that sulfur was mostly of magmatic origin with a minor contribution from sedimentary rocks. Our data suggest that the boiling of fluids formed an intermediate-sulfidation style of epithermal mineralization for the Mahour deposit.

Precipitation of Ag-Pb-Zn ores of the Poshan vein deposit in the Qinling orogen (central China) by dilution of magmatic hydrothermal fluids

Abstract Constraints on the source, nature, and evolution of ore-forming fluids are crucial for better understanding the ore genesis and mechanisms that lead to metal precipitation. Here, we present results of in situ analysis for quartz oxygen isotopes and sulfide sulfur isotopes, combined with apatite U-Pb age and fluid inclusion data, to provide insights into the source and evolution of ore fluids of the Poshan Ag-Pb-Zn vein deposit in the Qinling orogen, central China. Quartz-carbonate-sulfide veins at Poshan are hosted in lower Paleozoic metavolcanic-sedimentary rocks and structurally controlled by fracture zones associated with the Heqianzhuang anticline. The Ag-Pb-Zn mineralization consists of three stages, which are represented by quartz-pyrite-arsenopyrite (stage I), quartz-carbonate-sulfide-silver minerals (stage II), and quartz-calcite ± native silver (stage III). Apatite texturally associated with galena from stage II has a U-Pb age of 125 ± 14 Ma (2σ; mean square of weighted deviates [MSWD] = 0.9), which suggests that the Poshan deposit formed in the Early Cretaceous and thus significantly postdated the Paleozoic and early Mesozoic orogenic deformation of the Qinling orogen. Aqueous-carbonic fluid inclusions from stages I and II have similar total homogenization temperatures of 263–347 °C and calculated salinities of 1.2–5.1 wt% NaCl equivalent, whereas the values for liquid-dominated aqueous inclusions from stage III are 211–245 °C and 0.5–3.0 wt% NaCl equivalent. Five quartz generations are recognized from the three paragenetic stages, including Qz-1 and Qz-2 from stage I, Qz-3 and Qz-4 from stage II, and Qz-5 from stage III. Based on in situ secondary ion mass spectrometry oxygen isotopic analysis of the five quartz generations (Qz-1 to Qz-5), the calculated δ18Ofluid values for the ore fluids are 7.8‰ to 9.2‰ (mean 8.3‰), −3.2‰ to 8.7‰ (mean 5.6‰), −3.5‰ to 7.4‰ (mean 4.6‰), −4.5‰ to 7.6‰ (mean −0.2‰), and −6.4‰ to 1.4‰ (mean −3.8‰). The oxygen isotopic data and trend among the five quartz generations are best interpreted to represent magmatically derived ore fluid being diluted by modified meteoric water to cause mineralization. Fluid mixing is considered to be the principal mechanism that led to Ag-Pb-Zn precipitation at Poshan. Sulfides coexisting with the quartz generations have δ34SV-CDT values of −1.7‰ to 4.4‰, with no systematic variations among different paragenetic stages. These data, combined with apatite U-Pb age and geologic relations, provide additional evidence for a magmatic origin of the Poshan Ag-Pb-Zn deposit, as inferred from the oxygen isotopes. This study highlights the role of fluid dilution in triggering Ag-Pb-Zn deposition, and sheds light on the origin of silver-polymetallic deposits in orogenic belts.

Genesis and evolution of the Natividad Au-Ag(-Ge) epithermal deposit in southern Mexico: Unravelling the final chapters of the Sierra Madre del Sur metallogeny

The final magmatic arc—Miocene in age—of the long-lived Sierra Madre del Sur igneous province in southern Mexico hosts several epithermal deposits that have hitherto received little attention. The Natividad Au-Ag(-Ge) epithermal deposit is one of them and holds a mining record of > 200 years. Here, we present the first petrogenetic and metallogenic study on the Natividad deposit, in which we use a multi-methodological approach to assess the genesis and evolution of the deposit and its associated igneous rocks. Natividad is mostly hosted by Oligocene–Miocene arc-related dacites (U-Pb zircon dates of 22.8–24.7 Ma), whose geochemical features suggest lower-crustal differentiation (i.e., involvement of garnet) at the base of a thickened continental crust. The mineralization occurs in three multi-stage quartz + carbonate veins and consists of Fe-poor sphalerite (<5 mol. % FeS), galena, chalcopyrite, acanthite, and marcasite (sulfide-dominated stage) overprinted by pearceite-polybasite, pyrargyrite-proustite, tetrahedrite-group minerals, electrum, and argyrodite (Ag8GeS6; Ag-sulfosalt-dominated stage). Geothermometry and fluid inclusion data for ore-bearing assemblages reveal fluid temperatures of 170°–400 °C and salinities of 14.6–19.5 wt% NaCl equiv. δ18O from 0.8 ‰ to 7.5 ‰ in mineralizing fluids suggests mixtures of magmatic brines and meteoric waters, while δ13C from –8.4 ‰ to 2.2 ‰ indicates the recycling of organic carbon from the meta-sedimentary basement. Further, δ34S from –3.2 ‰ to –0.3 ‰ in sulfides attest to magmatic S. These results align with an intermediate-sulfidation epithermal model, whereby upwelling magmatic ore-bearing brines precipitated the ores due to conductive cooling, dilution, and, locally, boiling. Our study highlights the metallogenic potential of Miocene magmatism in the eastern Sierra Madre de Sur.

Timing and Mechanism of Ore Precipitation in Porphyry Cu Systems: Insight from LA-ICP-MS Analysis of Fluid Inclusions and In Situ Oxygen Isotope Analysis of Hydrothermal Quartz at Zhunuo Porphyry Cu Deposit, China

Abstract The timing and mechanism of ore precipitation in porphyry copper systems are hot topics and remain controversial. The large Miocene collision-related Zhunuo porphyry Cu deposit in the Gangdese belt of southern Tibet, China, was produced by multistage quartz veining and hydrothermal alteration, accompanied by Cu sulfide precipitation. In this study, we have combined cathodoluminescence (CL) petrography with in situ oxygen isotope analysis and fluid inclusion microthermometry and laser ablation-inductively coupled plasma-mass spectrometer microanalysis to constrain the growth history of individual quartz veins, the source and evolution of the hydrothermal fluids, and the timing and mechanism of ore precipitation at Zhunuo. Early quartz A veins associated with potassic alteration are composed of quartz, K-feldspar, biotite, Cu-Fe sulfides, and pyrite. Quartz B veins are composed of quartz, Cu-Fe sulfides, molybdenite, and pyrite. CL imaging shows that quartz grains in the A and B veins consist of abundant early generation of bright-luminescent quartz (QA and QB) with volumetrically minor later generation of dull-luminescent quartz (QA-crack and QB-crack) occurring in the voids or at the margins of the QA and QB veins with embayed contacts. Cu-Fe sulfides are generally in contact with the dull-luminescent quartz and locally in contact with the bright-luminescent quartz and K-feldspar in the A and B veins or occur as disseminations in the potassic-altered porphyries that have been overprinted by chlorite ± muscovite alteration. QA and QB contain single-phase intermediate-density inclusions and abundant brine and vapor-rich inclusions. A boiling assemblage in QA has a homogenization temperature of ~560°C and trapping pressure of ~530 bar. Two boiling assemblages in QB have homogenization temperatures of ~440°C with trapping pressures of ~230 and ~250 bar, indicating a transition from lithostatic to hydrostatic conditions at a paleodepth of ~2.0 to 2.5 km. QA-crack and QB-crack contain aqueous inclusions with lower homogenization temperatures of 340° to 400°C and salinities of 6 to 12 wt % NaCl equiv. In situ oxygen isotopes indicate that QA and QB have δ18O values of 7.6 to 11.4‰, whereas QA-crack and QB-crack have δ18O values of –7.2 to 6.7‰. Combined with fluid inclusion compositions, we propose that condensation of vapors into brines and mixing with 25 to 60% meteoric water can produce the salinity and oxygen isotopes of fluids that caused the dissolution of the early bright-luminescent quartz and the precipitation of the later dull-luminescent quartz. Zhunuo Cu-Fe sulfides are in contact with the bright-luminescent quartz and cut the growth bands. The dull-luminescent quartz in contact with the Cu-Fe sulfides has oscillatory growth banding. In addition, Cu-Fe sulfides in the A and B veins or in the potassic-altered rocks coexist with chlorite ± muscovite alteration minerals. These geologic observations, together with evidence that there is an abrupt drop in the Cu/(Na + K) ratio by more than one order of magnitude in the aqueous fluids within the dull-luminescent quartz compared to the brines within the bright-luminescent quartz, indicate that precipitation of Cu-Fe sulfides occurred after the potassic alteration stage and during the chlorite ± muscovite alteration stage. Ore precipitation was associated with mixing of magmatic fluids (brines + vapors) with meteoric water, accompanied by fluid cooling, salinity decrease, and retrograde quartz solubility as the rocks transitioned from lithostatic to hydrostatic conditions. During continued cooling in the latest stage, the hydrothermal fluids precipitated D veins that contain abundant pyrite with minor quartz. Quartz in the D veins (QD) contains aqueous inclusions with much lower temperatures and Cu/(Na + K) ratios, indicating that most of the Cu-Fe sulfides have been precipitated during this stage.

The genesis of the Chakabeishan Li-(Be) pegmatite deposit in the northern Tibetan Plateau: Evidence from fluid inclusion and lithium isotope

The Chakabeishan (CKBS) deposit is a newly discovered pegmatite-type lithium-beryllium deposit in the northern Qaidam tectonic belt of the northern Tibet Plateau. In recent years, some studies have discussed the genesis of the deposit, but the topic remains unclear. This study constrains the genesis of CKBS deposit based on detailed field observations and mineralogical studies, and presents fluid inclusion data and Li isotopic compositions of Li-rich pegmatites and Li-poor pegmatites. The mineralization characteristics of CKBS deposit shows a trend from weak Be mineralization to Li mineralization in the south to north direction, which shows the magmatic differentiation feature. Four types of fluid inclusions are identified: (1) triphase crystal-bearing inclusions (type-1), (2) biphase CO2-rich inclusions (type-2), (3) biphase aqueous inclusions (type-3), and (4) monophase liquid inclusions (type-4). The Li-rich pegmatites mainly contain type-1 inclusions and type-2 inclusions, while Li-poor pegmatites contain type-3 inclusions and some type-4 inclusions. Microthermometric and Laser Raman spectroscopy analyses show that Li-rich pegmatites formed in a low to medium temperature (210.5 ∼ 381.3 ℃), low to medium salinity (5.23 ∼ 17.82 % NaCl equiv.) NaCl-H2O-CO2 system, whereas Li-poor pegmatites formed in a low to medium temperature (206.4 ∼ 413.4 ℃), low to medium salinity (1.05 ∼ 10.49 % NaCl equiv.) NaCl-H2O system, which indicates a fluid immiscibility between them. In addition, lithium is greatly enriched in Li-rich pegmatites under the positive effects of CO2. The Li-rich pegmatites display high Li content (8362.4 ∼ 15509.6 ppm) but low δ7Li values (1.61 ∼ 1.80 ‰). In contrast, the Li-poor pegmatites display low Li content (23.9 ∼ 231.9) but high δ7Li values (0.79 ∼ 12.32 ‰). This means that the lithium isotopic fractionation is produced by the melt-fluid immiscibility in CKBS deposit, in which a Li-rich system with rich water and poor silicate and a Li-poor system with poor water and rich silicate were formed during the process. Therefore, the CKBS deposit may have formed under the combined effects of magmatic differentiation, melt-fluid immiscibility, and fluid immiscibility.

A contribution to the understanding of the origin of the Ginebra Gold District mineralizations, Colombia

Ginebra´s gold mineralization is hosted by the Ginebra Ophiolitic Massif and the Buga Batholith, in the western flank of the Central Cordillera of Colombia. Gold occurs as disseminations, quartz-carbonate stockwork veinlets and quartz lodes with a strong structural control and are composed by small amounts of sulfides, mostly pyrite, with galena, sphalerite and chalcopyrite in at least two different deposition events and related to strong sericite-chlorite-epidote haloes, indicative of near-neutral and reduced fluids. Petrography and Raman spectroscopy allowed to identify two main fluid inclusions assemblages primary to pseudo-secondary in origin, both of them aqueous and CO2-rich, with variable N2. Microthermometric analysis indicates the hydrothermal fluids associated with the gold were low saline (0.75-6.22 wt% NaCl equiv.) and presented a minimum trapping temperature ranging from 237.4 to 301.6°C. Petrography and microthermometric results suggest an isothermal fluid mixing and/or H2S loss as the main mechanisms related to gold bi-sulfide/thio-sulfide complexes destabilization and precipitation. Sulfur isotopes indicates a close to zero range (-8.2-+4.8‰), suggesting a restricted fluid circulation through the magmatic rocks of the Buga Batholith and the Ginebra Ophiolitic Massif. Besides, the oxygen and deuterium isotopes from hydrothermal sericite and chlorite accompanying to gold events, indicates a metamorphic origin for the hydrothermal fluids. 40Ar-39Ar dating of the hydrothermal alteration haloes, from El Retiro and La Esperanza, indicates a late Cretaceous-Paleocene age, between 67 and 65 Ma, contemporaneous with a regional strong dextral transpressive deformation related to subduction to obduction and exotic terrane accretion against the north-western part of the South American Plate. Although the hydrothermal fluid characteristics of the Ginebra Gold Disctrict are compatible with both the Intrusion-Related and Orogenic Gold deposit types, the metamorphic nature of the hydrothermal fluids and the tectonic regime at the time of mineralization event, allow us to propose they are compatible with an Orogenic Gold deposit.

Neoproterozoic-Early Cambrian Northern Chah-Farsakh Cu-Zn VMS-type deposit, Iran: Constraints from geology, geochemistry, fluid inclusions and geodynamic

Northern Chah-Farsakh is the first seafloor VMS described in the Torud-Chahshirin metallogenic belt of Iran. The deposit is hosted by Neoproterozoic-Early Cambrian mafic (basaltic andesitic)-siliciclastic rocks in volcano-sedimentary basin. The evolution of the ore-bearing basin is governed by the Proto-Tethys Oceanic crust subduction beneath the Central Iranian microcontinent. Three ore facies can be distinguished based on the ore textures studies: stringer zone ore facies, massive-replacement ore facies, bedded ore and distal facies. Pyrite, chalcopyrite, magnetite and sphalerite are the main minerals, together with minor amounts of pyrrhotite, bornite, tetrahedrite and tennantite. Textures include laminated, banded, replacement, massive, and vein-veinlet texture. There is a distinct metal zonation in the massive sulfide orebody; Gold, Ag, and Zn contents increase vertically from the stringer to the bedded ore facies; Cu and Co increase in the massive ore facies, and Pb is highest in the stringer zone. Ore mineralization in the Northern Chah-Farsakh deposit has emplaced in two stages. The fine-grained ore bands (stage 1) which are intricately interlayered with host rock beds, exhibit sedimentary structure such as laminae and bedding are consistent with a syn-sedimentary origin. Coarser-grained stage 2 ores have massive and vein-veinlet textures that are considered to form by replacement during sub-seafloor fluid flow. Based on SEM-EDS analysis, significant compositional variations were observed in the Py-1b grains. Py-1b is enriched in Pb compared to Py-1a. The elemental distribution map shows that the chalcopyrite (Cpy-2) minerals in Northern Chah-Farsakh deposit do not have variable composition and are homogeneous. Fluid inclusions in quartz minerals rom the footwall stringer zone have trapping temperatures between 203 and 500 °C with salinities (3.39–16 wt% NaCl equiv.) higher than modern seawater. Fluid inclusion studies suggest that the ore-forming fluids were derived from seawater. High level of Se in the massive ore facies of the Northern Chah-Farsakh supports the formation of mineralization from a high-temperature hydrothermal fluid. The Northern Chah-Farsakh Cu-Zn VMS deposit typify the mafic-siliciclastic type (Besshi-type), where the majority of the host stratigraphy is composed of a mafic flow-volcaniclastics and sedimentary rocks.

Nature, source, and evolution of the ore-forming fluids in the Dunbasitao gold deposit, East Junggar, China: Constraints from geology, fluid inclusions, and C-H-O isotopes

The origin of CO2-dominated fluids in orogenic gold deposits is usually mired in controversy. The Dunbasitao gold deposit is the largest among several gold deposits along the Armantai suture zone, East Junggar, China. Orebodies are hosted in volcano-sedimentary rocks of the Lower Carboniferous Jiangbasitao Formation and porphyritic quartz diorite and are controlled by shear zones. Based on the cross-cutting relationship of veins, the hydrothermal process can be divided into the early, middle, and late stages and the gold only occurred in the middle stage. Seven types of fluid inclusions (FIs) were identified in the Dunbasitao deposit: Type-1 FIs (LH2O + LCO2 or LH2O + LCO2 + VCO2) that homogenized to H2O phase or show critical homogenization; Type-2 FIs (LH2O + LCO2 or LH2O + LCO2 + VCO2) that homogenized to CO2 phase; CO2-dominated Type-3 FIs (LCO2 or LCO2 + VCO2); Two-phase aqueous Type-4 FIs (LH2O + VH2O) that homogenized to liquid phase; Type-5 FIs are composed of three phases (LH2O + VH2O + Solid), which homogenized to liquid phase; Type-6 and Type-7 FIs refers to FIs composed of a single liquid or vapor H2O phase, respectively.Microthermometry and laser Raman spectroscopy (LRS) analyses show that the initial ore-forming fluids in the early stage were moderate-Th (326–342 °C), low salinity (2.4 to 4.7 wt% NaCl equiv), and homogenous H2O−CO2−NaCl liquid fluids, containing 13–33 mol% CO2 and a small amount of CH4, H2S, and N2. The calculated δ18OH2O (V-SMOW) values are 7.5–8.5 ‰, δ18DH2O (V-SMOW) values range from −100 to −96 ‰, and δ13Cfluid (PDB) range from −3.8 to −2.5 ‰. In the middle stage, two typical immiscible fluid inclusion assemblages (FIA.18 and FIA. 27) composed of both Type-1 and Type-2 FIs were measured. The salinity of FIA.18 is 3.3 wt% NaCl equiv. and Th is 320 °C. For FIA.27, the salinity is 2.2 wt% NaCl equiv. and Th is 298 °C. The salinities of Type-4 FIAs vary from 5.9 to 14.4 wt% NaCl equiv., significantly higher than Type-1 and Type-2 FIs (1.7 to 3.5 wt% NaCl equiv). The salinities of three isolated Type-5 FIs (halite-bearing) range from 30.3 to 32.9 wt% NaCl equiv. and Th vary from 257 to 277 °C. These facts indicate extreme unmixing between carbonic and aqueous fluids in the middle stage, which led to gold precipitation. The Type-3 FIs represent the salt-free, H2O-lost, CO2 end-member composition, whilst the Type-5 FIs and high-salinity Type-4 FIs represent the highly saline aqueous end-member composition. Late-stage fluids are initially liquid, very low-salinity (1.4 to 2.6 wt% NaCl equiv), and low-Th (176–233 °C) aqueous fluids.Two immiscible carbonic FIAs from the middle stage yield a trapping pressure (Pt) of 86.9–133.9 MPa. Considering the rapid pressure fluctuations during fluid immiscibility, using hydrostatic or lithostatic pressure alone cannot get the real mineralization depth, Therefore, we use the lithostatic pressure for the Pt maximum and hydrostatic pressure for the Pt minimum and calculated a mineralization depth of 5.3–8.9 km, which doesn't represent the change but uncertainty for depth. Combining the characteristics of ore-forming fluids with the hydrothermal alteration and mineral compositions of ores, the Dunbasitao gold deposit is determined as a mesozonal orogenic gold deposit and there is considered to be prospecting potential in the deep.

The formation mechanism of the Xilekuduke porphyry Mo‐Cu deposit, NW China, revealed by the fluid inclusions and H‐O‐S isotopes

AbstractThe Xilekuduke porphyry Mo‐Cu deposit is located in the Altay‐East Junggar region of the Central Asian Orogenic Belt, northwest China. The orebodies occurring as vein type are host within the monzogranite and granite porphyry. Ore minerals include mainly molybdenite, pyrite, and chalcopyrite, whilst the major alteration include potassic, sericite, carbonate, and silicic. Mineralization can be divided into three stages: quartz‐K‐feldspar–polymetallic stage (Stage I), quartz‐polymetallic stage (Stage II), and quartz–calcite–pyrite (minor) stage (Stage III). Three types of fluid inclusion are present in the Mo‐Cu sulfide–calcite–quartz veins: CO2‐bearing (C‐type), aqueous (W‐type), and daughter mineral‐bearing (S‐type). Petrographic and microthermometric analyses of the fluid inclusions yielded homogenization temperatures for Stage I, II, and III to be 402–499°C, 214–391°C, and 136–254°C, respectively, with corresponding salinities of 39.2–59.6, 3.7–44.9 and 4.1–14.4 wt% NaCl equivalent. The δ18OH₂O and δD values of fluid inclusions in quartz are determined to be 5.3–6.0 ‰ and −76 to −60 ‰ (Stage I), 1.7–3.2 ‰ and −96 to −90 ‰ (Stage II), and −2.6 to −2.4 ‰ and −106 ‰ (Stage III), respectively. These results indicate that the primary ore‐forming fluids (stages I and II) were derived from granitic magma and were mixed with meteoric water in stage III. For the sulfide and sulfate (anhydrite), their δ34S values are of 0.4–5.8 ‰, 13.9–14.4 ‰, respectively, also that suggest a magmatic source. Fluid immiscibility, meteoric water interaction, and ore fluid‐wallrock interactions may have been critical for molybdenum precipitation.

Capitana mine, Tignamar district, a unique tin – bismuth concentration in the Chilean Central Andes, 250 km west of the Bolivian Tin Belt: Link to the Proterozoic-Paleozoic basement Belen inlier and the Arequipa-Antofalla terrane, a probable remnant of Laurentia

The Capitana mine, Tignamar District, is a unique Sn-Bi concentration in the highlands of Arica, in the Chilean Central Andes. Tin deposits associated with Triassic to Pliocene age igneous rocks are plentiful in the Tin Belt of Peru, Bolivia, and NW Argentina, but have not been reported in Chile, where contemporaneous rocks formed metallogenic belts rich in Fe, Cu, Mo, Ag and Au. We describe vein ore from Capitana mine, a small but exceptional Sn-bearing Pb-Bi-Ag-Cu-Sb-As epithermal deposit in the Tignamar (or Ticnamar) district in the high Andes of Arica, Chile, ca. 250 km west of the Bolivian Tin Belt. Fluid inclusions in vein quartz trapped a non-boiling, low salinity (<∼4 wt% NaCl equiv.), moderate T fluid (minimum T ∼ 220 °C) prior to metal precipitation. Flashing of this fluid, likely due to rapid changes in confining P, was synchronous with metal deposition; sulfosalt textures show evidence of syn-deformational growth. Although located within a district considered a porphyry copper system of Early Miocene age, it is likely that the Capitana deposit formed later, mainly as a result of regional hydrothermal activity related to compressive and transpressional tectonics as young as Pliocene. Common lead is 206Pb/204Pb 18.18; 207Pb/204Pb 15.61; and 208Pb/204Pb 38.53, significantly less radiogenic than that of Bolivian Sn deposits, and has a Paleozoic model lead age. These values point to affinities with a tectonically-emplaced inlier of crystalline basement of Proterozoic – Early Paleozoic age known as the Belen Metamorphic Complex, and with the Arequipa-Antofalla basement terrane, a probable remnant of Laurentia (North America), left behind during the dismemberment of the Rodinia Supercontinent. The complex mineralogy of Capitana vein, unlike other Chilean deposits, includes various sulphides and sulphosalts with Cu, Fe, Zn, Pb, Bi, Sn, Ag, As, Sb, Ga and In, and is exceptionally rich in U.