δ34SCDT Values Research Articles

Geological characteristics and ore‐forming conditions of the Tasikmadu porphyry Cu–Au prospect in Trenggalek, East Java, Indonesia

Tasikmadu is a newly discovered porphyry Cu–Au prospect in the eastern Sunda arc, Indonesia. This study aimed to elucidate salient diagnostic characteristics and ore‐forming conditions of the prospect. Fieldwork and various laboratory analyses for a suite of representative samples were performed for mineralogy, bulk‐geochemistry, mineral chemistry and ore fluid characterization. The study area is composed of three diorite porphyries, that is, fine‐grained, medium‐grained and coarse‐grained diorite porphyry, respectively. The intrusions are calc‐alkaline with a high Sr/Y value, which is similar to many ore‐bearing intrusions in the eastern Sunda arc. Ore mineralization occurs in quartz veins and veinlet stockwork, centred in the potassic zone, and dominated by chalcopyrite and bornite occurring in A and B veins, which cut earlier barren (EB) and M veins. The mineralization core has an average grade of 0.63 wt% Cu and 0.25 ppm Au, respectively. Outwardly, the potassic zone changes to the propylitic zone, which still bears copper in the quartz and pyrite veinlets, although the grade is low. Fluid inclusion microthermometry revealed that the A and B veins in the potassic zone formed at 464 and 390°C by hypersaline boiling fluids, respectively. The temperature temporally and spatially decreased, that is, in the propylitic zone, the quartz veinlets formed at 260–400°C. Hypogene mineralization that formed the A veins occurred at 1.5 km below the palaeosurface, indicating a relatively shallow depth as a porphyry deposit. Nevertheless, the δ34SCDT values of sulphides range from −2.0 to −0.1‰, inferring a magmatic origin. The Tasikmadu prospect shares some similarities compared with other porphyry deposits worldwide, but it also reveals unique characteristics that differ from others, for example, potassic‐altered rocks are only typified by secondary biotite without/rare secondary K‐feldspar reflecting the lack of magma contamination by continental crustal components. In addition, current surface geological features and shallow depth erosion level of the prospect may imply that the potential of Cu–Au mineralization underneath is still open to depth.

Genesis of sediment‐hosted copper and silver mineralization at the Omatapati prospect, Kaoko Belt, Opuwo district, Kunene region, Namibia

AbstractThe Omatapati copper and silver prospect within the Kaoko Belt is located in the Opuwo district, Kunene region, Namibia. The prospect is hosted by dolomite and interbedded argillites of the Neoproterozoic Devede Formation, the Ombombo Subgroup. An ore body is exposed in shallow artisanal mining pits and drill‐cores of the prospect have grades of 0.4 to 5.2 wt% Cu, and 23 to 312 g/t Ag. The prospect was formed by both hypogene and supergene mineralization processes. The hypogene mineralization occurred in three stages. Stage 1 is represented by calcite veins containing chalcopyrite, bornite, sphalerite and galena. Stage 2 consists of quartz and calcite veins with chalcopyrite and bornite. Stage 3 consists of quartz‐calcite‐barite veins with chalcopyrite. The veins of stages 1 and 2 are subparallel or discordant to the foliation of argillites, and those of Stage 3 are NE‐striking and steeply dipping in the brecciated dolostone and argillite. The mineralization stages 1, 2, and 3 are overprinted by supergene chalcocite, digenite, annite, covellite, malachite, delafossite, hematite, and goethite. The supergene process forms a semi‐massive chalcocite‐covellite zone, which extends from the surface to ~50 m depth. The veins show average concentrations of 2.1 wt% Cu, 80 ppm Ag, and 532 ppm Pb for the stage 1, 3.1 wt% Cu, 118 ppm Ag, and 66 ppm Pb for the stage 2, and 18.6 wt% Cu, 675 ppm Ag, and 565 ppm Pb for the Stage 3 with supergene overprinting. Silver occurs as impurity in supergene chalcocite (6303 ppm Ag), digenite (4425 ppm Ag), and covellite (3060 ppm Ag). Fluid inclusions in quartz and calcite revealed that the hypogene mineralization occurred under a pressure >7–8 MPa. Temperatures of ore formation of the stages 1, 2, and 3 were >145–155 °C, >290–300 °C, and >190–230 °C, respectively. Large variation of salinities in each fluid inclusion assemblage suggests fluid mixing and dilution processes. Fluid inclusion gas compositions in the Stage 3 have weighted means of 98.98 mol% H2O, 0.75 mol% N2, 0.52 mol% CO2, 0.02 mol% CH4, 0.0021 mol% Ar, 0.0009 mol% H2S, and 0.00006 mol% He and indicate a signature of magmatic fluids mixed with meteoric waters or seawater. δ34SCDT values of sulfides in the stages 1, 2, and 3 in the prospect have three data clusters, (1) near 0 ‰ of chalcopyrite in the stages 1 and 2, (2) near −11 ‰ of bornite in the stage 2, and (3) +5 to +11 ‰ of the supergene chalcocite and covellite. Modes of occurrence of ores, fluid inclusions and sulfur isotope data show that the prospect is likely the same type as sediment‐hosted copper‐silver deposits with veining found in the Central African Copperbelt.

Characteristics of the Kematu epithermal gold deposit at Tboli, Mindanao, Philippines

AbstractThe Kematu Au‐Ag epithermal deposit at Tboli area, Province of South Cotabato, Mindanao, Philippines, contains an inferred mineral resource of 3.8 million tonnes, at 8.7 g/t Au and 27 g/t Ag in 2012. The deposit is spatially and genetically linked to the volcanism related to the Parker Volcanic Complex of Pliocene to Holocene age. Local extension of the northwest‐trending splays of the faults in the Tboli area are associated with epithermal mineralization, including the Kematu Au‐Ag deposit. The study aimed to provide a detailed description of the characteristics and physicochemical processes involved in the formation of the Kematu Au‐Ag deposit on the basis of field occurrence, mineralogy, ore composition, mineral chemistry, and sulfur isotope data. The deposit is characterized by Au‐Ag bearing quartz‐adularia‐clay‐sulfide veins hosted in argillic‐altered andesite porphyry and coarse tuff of the Parker Volcanic Complex. The mineralization in the Kematu deposit is in the form of veins as well as open space fill and dissemination. Based on the observation of the ore bodies and petrographic analysis, three paragenetic stages with different vein characteristics have been identified. Stage 1 is dominantly quartz, adularia, and clay mineral veins, with electrum, sphalerite, pyrite, chalcopyrite, tetrahedrite‐tennantite, and galena. Stage 2 is coarse‐grained sulfide‐quartz‐adularia veins and in‐fill of vugs, consisting of sphalerite, pyrite, chalcopyrite, galena, tetrahedrite‐tennantite, and electrum. Stage 3 is massive calcite veins, with minor amounts of electrum, sphalerite, pyrite, chalcopyrite, and galena. The alteration mineral assemblage of the host rocks is chlorite‐illite‐adularia, indicative of neutral pH conditions. The FeS content of the Fe‐poor sphalerite in the stage 2 ranges from 0.03 to 1.07 mol%. Sulfur isotope compositions (δ34SCDT) of sulfides in all the stages range from 0.1‰ to 1.9‰ for pyrite, and −5.3‰ to 0.5‰ for galena, sphalerite, and chalcopyrite, where those in the stage 2 tend to have relatively lower values compared to those in the stages 1 and 3. The relatively narrow and close to zero δ34SCDT values suggest that the sulfur was mainly derived from a magma. The mineral assemblages of the stages 1, 2, and 3, and the sulfur fugacity (log fS2 = −12.5 to −8.8) and temperature (200–280°C) of ore formation based on the FeS mol%, electrum composition (at.%), and alteration mineral assemblage suggest that the Kematu deposit is of intermediate sulfidation type.

Genesis of the Mount Colin Cu-Au deposit, NW Queensland: Evidence from geology, multi-mineral U–Pb geochronology, S-, O- and C-isotope constraints

The Mount Colin Cu-Au deposit is located in the Mary Kathleen Domain of the Mount Isa Inlier, NW Queensland. The deposit is hosted in the Corella Formation, which transitions into the Burstall Granite at a depth of ~400 m. The host rocks of the deposit are overprinted by Na-Ca alteration and a Ca-Mg-Fe skarn assemblage. Na-Ca alteration yields a titanite 207Pb/206Pb weighted mean age of 1717 ± 8 Ma (MSWD = 0.32) and is composed of albite, actinolite, zircon, titanite and scapolite with retrograde calcite, prehnite and sericite. The Ca-Mg-Fe skarn yields a titanite 207Pb/206Pb weighted mean age of 1712 ± 7 Ma (MSWD = 1.2) and is composed of hastingsite, K-feldspar, clinopyroxene, albite, titanite, calcite, biotite, and zircon with retrograde quartz and chlorite. Based on temporal relationships, Na-Ca alteration and the Ca-Mg-Fe skarn is interpreted to have formed from a hydrothermal magmatic fluid during late-stage magmatism of the (1740–1710 Ma) Wonga-Burstall plutons. A second generation of titanite (denoted titanite II) is present within Na-Ca alteration and the Ca-Mg-Fe skarn assemblage. Titanite II yields a 207Pb/206Pb weighted mean age of 1576 ± 7 Ma (MSWD = 0.37), and is interpreted to have formed from an external metamorphic hydrothermal fluid during widespread deformation associated with the (1610–1500 Ma) Isan Orogeny. The Mount Colin Cu-Au deposit consists of a predominantly coarse-grained, mineralogically zoned assemblage that infills along the NW-striking Mount Colin Fault. The centre of the deposit comprises a largely unmineralized core composed of calcite and/or quartz ± apatite ± microcline. Cu-Au mineralization is positioned along the outer margins of the deposit and consists of biotite, actinolite, chalcopyrite and pyrrhotite with trace abundances of magnetite, pyrite, galena, melonite and arsenopyrite. Apatite from the core of the deposit yields a U–Pb age of 1523 ± 16 Ma (MSWD = 1.2). The δ34SCDT values of chalcopyrite and pyrrhotite range from 0.1–2.1 ‰ and 0.9–1.5 ‰ respectively. The δ13CVPDB values of calcite range from −5.54 ‰ to −4.54 ‰ with corresponding δ18OVSMOW values ranging from 8.16–11.26 ‰. Based on the temporal and isotopic constraints presented in this study, a hydrothermal magmatic origin for Cu-Au mineralization is favoured. The timing of Cu-Au mineralization is coeval with a regional-scale metamorphic/hydrothermal event throughout the Mary Kathleen Domain and widespread magmatism throughout the Eastern Fold Belt of the Mount Isa Inlier.

Non-magmatic sulfur source of hydrothermal colloform pyrite: Insights from the Jinshandian iron skarn deposit, Daye district, eastern China

Colloform pyrite occurs widely in many ore deposits in the Middle–Lower Yangtze River Metallogenic Belt (MLYRMB) in eastern China, but its genesis is still debated. In this study, we present detailed textures and geochemical compositions of newly identified colloform pyrite (Py1) and late coarse-grained pyrite (Py2) from the Jinshandian iron skarn deposit in the Daye district to decipher the genesis of the pyrite grains. Colloform pyrite is composed of nanometer-sized (<1 μm) grains, showing typical colloform textures, and occurs as interstitial fillings between magnetite grains. In contrast, Py2 commonly has a large grain size (up to 200 μm) and is usually distributed along the margins of colloform pyrite. These two types of pyrite have relatively high Co/Ni (1.24–13.36) ratios. δ34SCDT values of Py1 (17.22‰–20.63‰, mean 19.42‰) and Py2 (18.96‰–19.95‰, mean 19.43‰) are close to those of gypsum (anhydrite) from evaporites in the Daye district, indicating the incorporation of evaporite-derived materials into the formation of colloform pyrite. On the basis of the textures, trace-element compositions, and sulfur isotope characteristics of the colloform pyrite, it is inferred that this pyrite from the Jinshandian iron deposit is of hydrothermal origin. The sulfur isotope composition of colloform pyrite from Jinshandian is heavier relative to other magmatic-hydrothermal colloform pyrites, which indicates colloform pyrite could formed in diverse hydrothermal fluids (magmatic to no-magmatic fluid). Our study further confirmed that hydrothermal colloform pyrite has widely occurred in Fe and Cu-Au deposits associated with the Cretaceous magmatism in the MLYRMB.

The Sulfur Isotopic Characteristics of Evaporites in the Yarkand Basin of Xinjiang Province in the Paleocene and Its Paleoenvironmental Evolution

The Yarkand Basin, located in the southwest of the Tarim Basin, is a northeastern part of the eastern Paratethys ocean in the Paleocene, and a significant amount of evaporites, with gypsum, anhydrite, and halite as the main types, were developed in this area. These evaporites record the sedimentary environment at that time. A study was conducted on the sulfur isotopic composition of gypsum in the Paleocene of the Yarkand Basin to explore the origin of the evaporites and interpret the sedimentary environment. The experimentally measured sulfur isotope δ34SCDT values of 187 gypsum samples ranged from 6.69‰ to 25.92‰ with an average value of 18.64‰. The overall trend of the Paleocene gypsum sulfur isotopic curve is consistent with the global seawater sulfur isotopic curve, which shows a decreasing trend. In the early and middle Paleocene, the curve shows four stages of sulfur isotope increase, indicating that the sedimentary environment during that time was mainly influenced by bacterial reduction and a relatively open sedimentary environment, while the late period shows a decreasing trend, suggesting that the late period may be primarily influenced by terrigenous freshwater. In addition, the sulfur isotope value has the characteristics of decreasing from northwest to southeast of the basin, which may indicate that the sedimentary environment of Paleocene evaporites in the Yarkand Basin may also be related to paleotopography and distance from the estuary, resulting in differences in sedimentary environments. The mainly original sulfur isotope values of the Paleocene evaporites in the Yarkand Basin should be in the range of 18‰–20‰, which is a supplement to the Paleocene global paleoseawater and is of great significance for the reconstruction of the marine transgressive–regressive cycle and sulfur isotopic composition of the eastern Paratethys ocean during this period.

Gold mineralized diorite beneath the Linglong ore field, North China craton: New insights into the origin of decratonization-related gold deposits

Gold deposits in Precambrian cratons were mostly generated during the formation and stabilization of the cratons, but the North China craton is unusual in that its gold deposits were mainly formed ∼1.7 b.y. after its stabilization. A magmatic-hydrothermal origin or mantle-derived fluid source has been proposed for the giant gold deposits of the Jiaodong District in the eastern North China craton, but direct evidence is sparse, and the mineralization processes remain controversial. Here, we present the results of a comprehensive geological, geochronological, and geochemical study of the gold mineralized Xiejia diorite beneath the Linglong ore field at Jiaodong to link the gold mineralization to underlying magmatism. Magmatic zircon and titanite grains from the Xiejia diorite have laser ablation−inductively coupled plasma−mass spectrometry (LA-ICP-MS) U-Pb ages of 121.3 ± 0.9 Ma to 120.8 ± 1.1 Ma and 121.7 ± 3.9 Ma, respectively, which are indistinguishable from the time of gold deposition throughout the Jiaodong District as constrained by previous studies. The diorite has a shoshonitic composition and is characterized by strong enrichment in large ion lithophile elements (LILEs) and light rare earth elements (LREEs) along with significant depletion in high field strength elements (HFSEs) and heavy rare earth elements (HREEs). Samples of the diorite have high initial 87Sr/86Sr ratios, but low εNd(t) and ɛHf(t) values and low Pb isotope ratios. These geochemical characteristics are akin to those of contemporaneous mafic dikes in most gold mines at Jiaodong, indicating that the Xiejia diorite was most likely derived from an enriched lithospheric mantle source. The upper part of the diorite intrusion is pervasively altered and mineralized, containing an average of 0.32 g/t Au, but locally up to 7.59 g/t. Hydrothermal titanite from the mineralized diorite has a LA-ICP-MS U-Pb age of 122.3 ± 4.3 Ma, which is consistent with the gold-bearing pyrite Re-Os isochron age of 122.5 ± 6.7 Ma. Ore-related sericite aggregates from the Dongfeng gold deposit above the Xiejia diorite have a 40Ar/39Ar plateau age of 122.6 ± 1.3 Ma. Pyrite from the mineralized diorite yielded δ34SCDT values of 2.1‰−9.7‰, which are comparable with those of pyrite (δ34SCDT = 5.8‰−8.1‰, where CDT indicates the Canyon Diablo troilite standard) from gold ores of Dongfeng. Pyrite grains from both groups also have similar Pb isotope compositions. The S and Pb isotope data are consistent with values of mafic dikes that are spatially and temporally associated with gold veins in the Linglong ore field. The results presented here thus indicate a possible genetic link between gold mineralization in the Xiejia diorite and underlying magma presumably represented by the Xiejia diorite. The auriferous fluids exsolved from that magma and migrated upward along the Potouqing fault to form the Dongfeng gold deposit above the Xiejia diorite. The mineralized diorite thus links shallow gold mineralization to deep-seated mantle-derived magmatism generated during the extensive destruction of the North China craton induced by the rollback of the subducted paleo-Pacific plate.

Geology, geochemistry, and genesis of gold mineralization in the Chifumbazi deposit of the Tete Province, Irumide Belt, Mozambique

AbstractThe Chifumbazi gold deposit is located in the Chifunde District, Tete Province, northwestern Mozambique. The geology of the study area is composed of the Proterozoic Mualadzi Group comprising ultramafic metavolcanic rocks, quartzite, biotite‐schist, Macanda Mafic Metavolcanics, conglomerate, and granitoid of the Furancungo Suite. The geological characteristics and metallogenesis of gold mineralization in the Tete Province are poorly understood. This study describes the gold mineralization and associated hydrothermal alteration in the Chifumbazi deposit on the basis of petrography, whole‐rock geochemistry, mineral chemistry, fluid inclusion and sulfur isotope analyses. The mineralization in the Chifumbazi deposit includes auriferous quartz, calcite, dolomite and ankerite quartz‐chlorite, and chlorite‐pyrite veins and veinlets as well as sulfide dissemination hosted by altered meta‐granodiorite along shear zones and fracture zones. On a larger scale, the mineralized veins and veinlets occur along a discordant fracture system within a Pan‐African shear zone. The meta‐granodiorite host‐rock of the mineralization consists mainly of plagioclase, biotite, actinolite, and quartz, and alteration minerals calcite, dolomite, sericite, and chlorite. The meta‐granodiorite is enriched in LREE compared to HREE and shows negative Eu anomalies. The mineralization in the Chifumbazi deposit formed through three hypogene mineralization stages (Stages I–III) and one supergene stage (Stage IV). Stage I comprises quartz, calcite, dolomite, ankerite, pyrite, chalcopyrite, pyrrhotite and galena. Stage II comprises quartz, pyrrhotite, pyrite, chalcopyrite and native gold. Stage III comprises chlorite and pyrite; and Stage IV comprises secondary minerals goethite, bornite and covellite. Bulk chemical analysis of ores detected gold contents up to 5 ppm for a quartz vein of Stage II, where visible native gold is present in pyrite. The δ34SCDT values of pyrite and chalcopyrite of the Stages I–III range from +0.9 to +2.4 ‰. On the basis of the geological setting, mineralogy, and sulfur isotope signatures, the Chifumbazi deposit can be classified as orogenic.

Origin of the Woxi orogenic Au-Sb-W deposit in the west Jiangnan Orogen of South China: Constraints from apatite and wolframite U-Pb dating and pyrite in-situ S-Pb isotopic signatures

The majority of gold mineralization in the Jiangnan Orogenic Belt (JOB) of South China share similarities with the orogenic type, but the nature of mineralization remains controversial, especially in terms of intracrustal versus subcrustal origin of ore fluids and metals and their relationships with the subduction of the Paleo-Pacific plate. This paper reports results of in situ analyses of minerals closely related to gold mineralization, including U-Pb ages of apatite and wolframite, and S-Pb isotopes of pyrite, from the Woxi Au-Sb-W deposit in the western Jiangnan Orogen, and use them to address the above problems.The Woxi deposit, which consists of several auriferous quartz lodes hosted by ductile–brittle shear zones in the Neoproterozoic slate. The hydrothermal mineralization and alteration processes are divided into four stages. Early-ore stage (S1) is characterized by disseminated, euhedral, porous, coarse auriferous pyrite (Py1) with minor amounts of arsenopyrite, siderite, and rutile in the bleached slate. Main-ore stage (S2) is characterized by subhedral to euhedral, auriferous pyrite (Py2) with compositional zoning, with small amounts of wolframite and apatite in quartz veinlets. Late-ore stage (S3) is represented by scheelite and stibnite with minor amounts of native gold and anhedral, dendritic auriferous pyrite (Py3) in quartz veinlets. Post-ore stage (S4) features a quartz-calcite-barite-chlorite mineral assemblage that occurs as veinlets or in pressure shadows of Py1.Apatite and wolframite associated with Py2 yield a consistent U-Pb age of ca. 141 Ma, which is corresponded to a time when the Paleo-Pacific plate started to roll back, and a Basin-and-Range style tectonic regime began to developing in South China. The different stages of pyrite have variable S isotopes, with the δ34SCDT values (mainly between −6‰ and +1 ‰) largely overlapping with those of the metasomatized mantle (−5‰ ∼ + 5 ‰), and Pb isotope ratios between crustal and mantle values. Taking these results together, we proposed that the Woxi deposit and many other gold deposits in the JOB formed from subcrustal processes involving the metasomatized upper mantle above the subduction zone. Given the extended distance from JOB to the Paleo-Pacific plate boundary, the metasomatized mantle underneath the JOB is likely initially formed during the plate subduction leading to the formation of the JOB during the Neoproterozoic, which is further fertilized by upwelling asthenosphere due to rollback of the Paleo-Pacific plate in the Mesozoic.

Cu‐Isotope Evidence for Subduction Modification of Lithospheric Mantle

AbstractUltramafic xenoliths from southeastern Arizona, USA, provide evidence for Cu‐isotope heterogeneity in the lithospheric mantle. We report new data on Type I (Cr‐, Mg‐rich) peridotites, but also the first Cu‐isotope data for Fe‐Ti‐Al‐rich Type II pyroxenite (±amphibole) xenoliths. Whole rock δ65Cu values of the pyroxenites and cryptically metasomatized Type I lherzolites range to isotopically heavier compositions than asthenospheric mantle (i.e., up to +1.44‰ and +1.12‰, respectively, vs. ∼0‰ ± 0.2‰). Copper leached from the xenoliths using aqua regia, assumed to be hosted in interstitial sulfides, is even more variable (δ65Cu −0.78 to +3.88‰), indicating considerable isotopic heterogeneity within individual samples. Host basalts have low δ65Cu (−0.23‰ to −1.30‰), so basalt—xenolith interactions are not responsible for the compositional variations observed. While mass‐dependent fractionation may be partly responsible, metasomatism by fluids derived from recycled crustal materials is the predominant control on isotopic variations observed. Amphibole megacrysts and amphiboles separated from Type II amphibole‐bearing clinopyroxenite have normal, mantle‐like 18O/16O ratios but H‐isotope compositions (δ2HSMOW −82‰ to −45‰) that range between that of nominally anhydrous mantle (−80 ± 10‰) and seawater (0‰). Host basalts are also enriched in 34S relative to depleted asthenospheric mantle, having δ34SCDT values up to +8‰, i.e., compositions commonly attributed to a component of recycled seawater or hydrated oceanic crust. These new data suggest that formation of Type II metasomes in the lithospheric mantle beneath the Basin and Range Province was associated with subduction of the Farallon plate and not alkali basalt magmatism associated with Basin and Range extension.

Nature and evolution of the ore‐forming fluids in the Shazhou volcanic‐related hydrothermal uranium deposit, Xiangshan ore field, SE China

The Xiangshan uranium (U) ore field in South‐east China has been recognized as the largest volcanic‐related hydrothermal U deposit in China since its discovery in the 1950s. The U mineralization at Xiangshan is mostly hosted in felsic volcanic and sub‐volcanic rocks and occurs mainly in veins, which are controlled by high‐angle normal faults in association with haematite, quartz, fluorite, apatite, and pyrite. Likewise, diverse hydrothermal alterations such as haematitization, silicification, fluoritization, and illitization have been identified adjacent to the ore‐bearing faults and outward for tens to hundreds of metres into the volcanic rocks. Situated to the west in the Xiangshan ore field, the Shazhou deposit is the second‐largest U deposit in the Xiangshan volcanic basin. Based on geological field evidence and petrographic observations, the ore‐forming fluids in the Shazhou U deposit can be classified and separated into three stages (early, main, and late): (a) fluids associated with the early mineralization stage are characterized by the oxidizing feature with U‐O hydroxide complexes as the dominant species; (b) fluids from the main mineralization stage were reducing fluids with black–purple fluorite and sulphide complexes of U‐Ti‐O; and (c) fluids from the late‐stage were weakly oxidizing fluids with light purple fluorite and light red calcite complexes of U‐O as the dominant species in the fluid. Fluid inclusions in alteration minerals from the main and late mineralization stage recorded homogenization temperatures (Th) of 280–340°C and 200–260°C, with salinities of 5–17 and 6–10% NaCleqv, respectively. Ore‐forming fluids contain variable amounts of CO2, O2, and H2, in which the volatile content in the main mineralization stage is higher than that in the late stage. The temperature and salinity of the ore‐forming fluids were fluctuating and gradually decreased as the geologic history of the deposit progressed. The δDW‐SMOW values calculated for the ore‐forming fluids range from −97.4 to −65.1‰. The δ18O values of syn‐ore quartz occur mainly between 5.9 and 15.7‰; calculated δ18OW‐SMOW values are between −1.5 and +8.3‰. The δ34SCDT values of syn‐ore pyrite and galena range from 9.7 to 19.7‰. The ore‐forming fluids in the Shazhou U deposit are derived from different sources with a complex geological evolution history. The ore‐forming fluids from the early mineralization stage with high O2 contents may have been primarily derived from post‐volcanic hydrothermal activity. Subsequently, fluids from the main mineralization stage (with lower O2 and high H2 contents) might have originated from the deep‐sourced fluids, where sulphur was carried from the metamorphic basement. Finally, ore‐forming fluids from the late mineralization stage could have been produced by mixing meteoric hydrothermal fluids. Large‐scale fluid immiscibility and boiling occurred during the main mineralization stage, followed by fluid mixing during the late mineralization stage. Boiling and mixing of fluids were the two dominant mechanisms for the deposition of U in the Shazhou deposit.

Geology, geochemistry and genesis of Keyue: A newly discovered Pb-Zn-Sb-Ag polymetallic deposit associated with magmatic center in Southern Tibet, China

The Keyue Pb-Zn-Sb-Ag polymetallic deposit is located within the North Himalayan Metallogenic Belt (NHMB). This study aims to clarify whether the Keyue deposit has close association in time and space with magmatism, and discuss the significance for further exploration. Orebodies are hosted by the Lower Jurassic Ridang Formation black carbonaceous slate and controlled by the NE-trending faults. Keyue is characterized by multiple stages of hydrothermal veins, including Mn-Fe Carbonate-sulfide (I), quartz-sulfide-sulfosalt mineral (II) and quartz-calcite-stibnite veins (III).Hydrothermal minerals contain six types of fluid inclusions, including H2O-rich bi-phase aqueous (type I), pure CO2 (type II), CO2-rich H2O-CO2-NaCl tri-phase (type III), H2O-rich H2O-CO2-NaCl tri-phase (type IV), halite-bearing tri-phase (type V) and halite-bearing H2O-CO2-NaCl multiphase inclusions (type VI). All six types of inclusions were observed in stage II quartz, whereas only types I and III inclusions in stage I siderite and sphalerite and type I inclusions in stage III quartz and calcite. Type I inclusions in stage I display total homogenization temperatures (Th, total) ranging from 250.1 to 289.3 °C, with salinities of 9.6–16.3 wt% NaCleq. Types I, III, IV and V inclusions in stage II yield Th, total of 175.5–282.7 °C, 188.8–286.3 °C, 214.3–287.5 °C and 198.3–266.0 °C, with corresponding salinities of 4.0–21.5 wt% NaCleq, 0.6–2.9 wt% NaCleq, 0.0–11.0 wt% NaCleq and 30.1–33.2 wt% NaCleq, respectively. Type I inclusions in stage III have Th,total values of 172.3–240.7 °C and salinities of 3.1–12.6 wt% NaCleq. Fluid phase separation occurred in stages I and II, resulting in CO2 and H2S release, pH increase and rapid Pb-Zn-Ag precipitation, whereas mixing of magmatic fluids and meteoric water in stage III caused the cooling, dilution and stibnite precipitation.Fluid inclusion analysis and C-H-O isotopic compositions indicate that the initial hydrothermal fluids were magmatic water, with increasing input of meteoric water with time. The δ34SCDT values of sulfides from three stages are similar and range from 4.8 to 10.3 ‰ (average 7.7 ‰), showing characteristics of mixture of magmatic and sedimentary sulfur. The Pb isotopic compositions of sulfides are closely consistent with those of Cenozoic leucogranite and Precambrian metamorphic crystalline basement in the NHMB, suggesting that the ore-forming metals were sourced from the hidden causative Himalayan leucogranite formed by the decompression melting of metamorphic crystalline domains.Combining evidence from geochronology, fluid inclusions, isotopes suggest that the Keyue Pb-Zn-Sb-Ag and Cuonadong W-Sn-Be mineralization at different locations around the Cuonadong Dome constitute an integrated magmatic-hydrothermal system, with the distal end-member Pb-Zn-Sb-Ag veins centered on the Cuonadong leucogranites-related W-Sn-Be mineralization. Pegmatite-skarn-type W-Sn-Be polymetallic mineralization may occur at deeper sites beneath the Keyue area, and the distal Pb-Zn-Sb-Ag veins controlled by faults within strata also need more attention around these leucogranite domes in the NHMB.

Constraining the genesis of tungsten mineralization in the Jiaoxi deposit, Tibet: A fluid inclusion and H, O, S and Pb isotope investigation

The Jiaoxi deposit, located in the western part of the Lhasa terrane, is the first discovered Miocene (ca. 13 Ma) quartz vein-type tungsten deposit in this belt. Ore bodies mainly occur as wolframite-bearing veins hosted in the shales and granite. Three stages were identified for the formation of the Jiaoxi deposit, including the oxide stage (dominated by wolframite and quartz), the sulfide stage (quartz-sulfides veins) and the fluorite stage (late veins comprising fluorite, calcite, and quartz). Here, we investigate the genesis of this deposit based on fluid inclusion and H-O-S-Pb isotope studies. Fluid inclusion microthermometry and oxygen isotope data reveal that the wolframite precipitated from a moderate temperature (340–380 °C), low salinity (2.1–7.5 wt% NaCl equivalent) hydrothermal fluid at a depth of ∼ 6 km. The sulfides from the oxide and sulfide stage have uniform δ34SCDT values (+2.5 to + 3.7‰), and consistent Pb isotope compositions with the coeval granites (206Pb/204Pb: 17.866–18.789; 207Pb/204Pb: 15.555–15.743; 208Pb/204Pb: 37.157–39.335). The δ18OVSMOW value of the hydrothermal fluid decreased from the oxide (δ18OVSMOW = +7.2 to +14.2‰) to the fluorite stage (δ18OVSMOW = +2.1 to +5.7‰), indicating that the exsolved magmatic hydrothermal fluid mixed with meteoric water. This is also suggested by the positive correlation between the salinity and homogenization temperature of the aqueous fluid inclusions. LA-ICP-MS analysis of individual fluid inclusion reveals that the W concentrations of ore-forming fluid in the oxide stage (1.2–70.2 ppm) are much higher than those in the sulfide and fluorite stage (1.1–2.2 ppm) and show positive correlations with the homogenization temperatures and the Cl concentrations. We propose that fluid dilution and cooling due to fluid mixing played an important role during the wolframite precipitation in the Jiaoxi deposit.

Zinc, cadmium and sulphur isotopic compositions reveal biological activity during formation of a volcanic-hosted massive sulphide deposit

Zinc and Cd isotopes fractionate strongly within a range of hydrothermal systems; consequently, metal stable isotopes have been used to understand the formation of hydrothermal ore deposits. We investigated the Zn–Cd–S isotopic compositions of sulphides from the Carboniferous-Permian Xiaobaliang Cu–Au deposit, Inner Mongolia, China. This ancient seafloor hydrothermal system is the only known Cyprus-type volcanic-hosted massive sulphide (VHMS) deposit in the Central Asian Orogenic Belt. The S isotopic compositions of sulphide minerals are highly variable with δ34SCDT values ranging from −21.2‰ to 25.2‰. We infer that negative δ34SCDT values reflect mixing of volcanogenic S and S derived from bacterial sulphate reduction (BSR), and that positive δ34SCDT values reflect mixing of volcanogenic S with S derived from thermochemical sulphate reduction (TSR). Zinc isotopic compositions are relatively consistent at the deposit; δ66Zn values range from 0.10‰ to 0.70‰. These values are similar to those reported for modern seafloor sulphides. We infer that consistency of δ66Zn values relates to the Zn species ([ZnCl4]2−) present in the ore-forming fluids during sulphide precipitation. All of the sulphides are enriched in the light Cd isotopes; δ114/110Cd values range from −0.74‰ to −0.08‰. Zinc and Cd can be affected by biological activity, and we infer that biological activity caused the negative δ114/110Cd values at this deposit because: (1) biological processes (e.g., bacterial activity) enrich fluids in the light Cd isotopes, leading to the precipitation of sulphides with negative δ114/110Cd values; and (2) the Cd isotopic composition of ore-forming fluid is readily modified because the concentration of Cd is much lower than that of Zn in ore and basalt. Our results indicate that Cd isotopes might record ancient biological activity, and that organisms might play a more important role than previously thought in the formation of VHMS systems.

Iron and sulfur isotopic compositions of carbonatite-related REE deposits in the Mianning–Dechang REE belt, China: Implications for fluid evolution

Carbonatite-related rare earth element (REE) deposits are the most significant source of REEs worldwide. The processes of REE precipitation, enrichment, and mineralization remain controversial. The Cenozoic Mianning–Dechang (MD) REE belt, located in Sichuan Province, southwestern China, comprises one giant (Maoniuping), one large (Dalucao), and two small–medium (Muluozhai and Lizhuang) deposits. These deposits provide a continuous record of fluid evolution, and thus are ideal for investigating the processes of REE mineralization in carbonatite-related REE deposits. Given that sulfate (i.e., barite and celestite) and sulfide (i.e., pyrite and galena) minerals crystallized and precipitated in the pegmatitic to hydrothermal stages, respectively, the REE minerals formed later than the sulfate minerals. However, the formation sequence of the sulfide minerals and bastnäsite is unclear, although both pyrite and bastnäsite formed in the late hydrothermal stage. We used S isotope data for sulfate and sulfide minerals and Fe isotope data for pyrite to investigate the composition and evolution of ore-forming fluids during the magmatic–hydrothermal stages. The sulfate minerals have positive δ34SCDT values (+3.2‰ to +8.3‰), and the sulfide minerals have negative δ34SCDT values (−13.5‰ to − 5.6‰) in the four REE deposits. In the Maoniuping deposit, δ34SCDT values for barite from the pegmatitic stage (+4.7‰ to +5.7‰) are higher than for barite from the hydrothermal stage (+4.1‰ to +4.5‰), which indicate that hydrothermal activity led to relative enrichment in isotopically light S. The δ34SCDT values for barite (+3.2‰ to +5.5‰) are lower than for celestite (+6.2‰ to +7.2‰) from the pegmatitic stage in the Dalucao deposit. The δ34SCDT values for galena (−13.5‰) are also lower than for pyrite (−13.5‰ to −7.2‰) from the hydrothermal stage in the Guangtoushan section. In general, δ34SCDT values change from positive to negative values (+8.3‰ to −16.4‰) as the fluids evolved from the pegmatitic to hydrothermal stages, which can be attributed to a decrease in oxygen fugacity (fO2) and addition of sediment containing isotopically light S. Iron isotopic compositions of pyrite from the hydrothermal stage show significant variations (δ56FeIRMM-014 = −0.03‰ to +0.65‰ for the Maoniuping deposit; −0.14‰ to 0.00‰ for the Dalucao deposit; +0.05‰ to +0.35‰ for the Lizhuang deposit), and are higher than those for the carbonatites (δ56Fe IRMM-014 = −0.47‰ to −0.17‰). These data indicate there are two sources of Fe in the MD REE belt, which are the carbonatite–nordmarkite magma and 56Fe-rich sediment. Paleozoic–Mesozoic volcanic–sedimentary and Mesozoic clastic and carbonate rocks are exposed in the MD REE belt. In general, the S–Fe isotope data, along with geological and petrographic observations, indicate that the REE minerals formed later than the sulfate minerals, and the S–Fe were derived from both carbonatite magma and sediment containing isotopically light S and heavy Fe.

Constraints of S–Pb–Sr Isotope Compositions and Rb–Sr Isotopic Age on the Origin of the Laoyingqing Noncarbonate-Hosted Pb–Zn Deposit in the Kunyang Group, SW China

The Laoyingqing Pb–Zn deposit is located on the southwestern margin of the Yangtze block and on the east side of the Xiaojiang deep fault in the Sichuan–Yunnan–Guizhou Pb–Zn metallogenic triangle area (SYGT). This deposit was first discovered in the silty and carbonaceous slate of the Middle Proterozoic Kunyang Group that is structurally controlled by thrust faults and anticlines. This study is aimed at investigating whether the Laoyingqing deposit has the same ore-forming age and type as other Pb–Zn deposits related to the Pb–Zn metallogenic system and prospecting prediction of the deep and peripheral areas of the deposits in the SYGT. Based on the sphalerite Rb–Sr age dating and S–Sr–Pb isotopic composition analysis of the Laoyingqing Pb–Zn deposit, the following results were obtained. First, the Rb–Sr isochron age of sphalerite is 209.8 ± 5.2 million years (Ma), consistent with the ages of most Pb–Zn deposits in the SYGT (approximately 200Ma), thereby potentially indicating that these Pb–Zn deposits may have been formed synchronously during the late Indosinian orogeny. Second, the Pb isotopic compositions of sulfides show a linear trend on the average crustal Pb evolution curve in 207Pb/204Pb vs. 206Pb/204Pb plot. In addition, Pb isotopic ratios were consistent with the age-corrected Pb isotopic ratios of basement rocks, consequently suggesting that the source of mixed crustal Pb is mainly derived from basement rocks. Combined with the initial 87Sr/86Sr ratios of sphalerite between the (87Sr/86Sr)200Ma value of the basement rocks and that of the Upper Sinian–Permian carbonates, it can be concluded that the ore-forming metals were mainly derived from basement rocks. Third, sulfur isotopic composition of sphalerite from the Laoyingqing deposits shows δ34SCDT values that range mainly from -2.62‰ to 1.42‰, which is evidently lower than the δ34SCDT values of sulfides (8–20‰) from other Pb–Zn deposits in the SYGT. This can be interpreted as a result of mixing with reduced S that was mainly derived from the thermochemically reduced S in the overlying strata and a small amount of reduced S produced by the pyrolysis of S-containing organic matter. We conclude that the Laoyingqing deposit and most of the Pb–Zn deposits in the SYGT are Mississippi Valley-type deposits, thereby providing new ideas for investigating the deep and peripheral areas of Pb–Zn deposits.

Genesis of the Nailenggele Mo-Cu-Pb-Zn polymetallic orefield in the Boluokenu Metallogenic Belt, Western Tianshan, China: Constraints from geochronology, fluid inclusions and isotope geochemistry

The Nailenggele orefield, located in the northwestern Chinese Tianshan Orogenic Belt, is composed of the Lailisigao’er Mo deposit, No. 3571 Cu prospect and Qixing Pb-Zn deposit. Lailisigao’er is a typical porphyry deposit with characteristic veinlet-disseminated ores and potassic, phyllic and propylitic alterations. No. 3571, situated in the peripheral of Lailisigao’er, is characterized by large amounts of oxidized ores at surface with limited intrusions outcropped. Qixing, about 3 km from Lailisigao’er, is characterized by quartz-sulfide veins controlled by fractures. This study aims to examine the genetic relationships between these deposits and/or occurrences, and discuss the significance for further exploration in the orefield and elsewhere in the region. LA-ICP-MS U-Pb dating on zircons from the ore-bearing porphyry in the Lailisigao’er deposit yielded an age of 367.5 ± 4.8 Ma. The molybdenite Re-Os and sphalerite Rb-Sr isochron ages recalculated from previously published data are 365.9 ± 2.1 Ma for Lailisigao’er and 362.0 ± 5.7 Ma for Qixing, respectively, suggesting that they are coeval and both related to the granodiorite porphyries. Three types of fluid inclusions occur in the Mo-bearing quartz from Lailisigao’er, including two-phase aqueous inclusions (Type I), solid mineral-bearing aqueous inclusions (Type II) and CO2-H2O inclusions (Type III). The total homogenization (Th) temperatures cluster from 260 to 320 °C (to liquid) for type I inclusions, 310 to 332 °C (to liquid) for type II inclusions, and 268 to 324 °C (to CO2 phase) for type III inclusions. The salinities are mainly in the ranges of 2.0–8.0, 32.9–42.0, and 1.4–5.5 wt% NaCleq for types I, II and III inclusions, respectively. By contrast, only type I inclusions were identified in the Pb-Zn-bearing quartz from Qixing, with Th values of 149–261 °C and salinities of 1.7–5.3 wt% NaCleq. The δ34SCDT values of hydrothermal sulfides from Lailisigao’er, No. 3571 and Qixing range from 2.8‰ to 4.0‰, 4.0‰ to 4.6‰ and 0.7‰ to 4.9‰, respectively. Sulfides from these three locations have uniform Pb isotopic compositions. The (87Sr/86Sr)0 ratios of fluid inclusions (average 0.70971) in Mo-bearing quartz at Lailisigao’er and sphalerite (average 0.71020) at Qixing are similar to those of Mo-mineralized porphyries (average of 0.70886) from Lailisigao’er. The δ18OH2O and δDH2O values of Pb-Zn-bearing quartz from Qixing are similar to those of Mo-bearing quartz from Lailisigao’er, both plotting close to the field of magmatic water but shifted toward the meteoric line. These geochronological, fluid inclusions and isotopic data suggest that the mineralization at different localities in the Nailenggele orefield constitutes part of an integrated magmatic-hydrothermal system centered on the Lailisigao’er porphyry Mo deposit, with the Qixing Pb-Zn polymetallic deposit representing a distal end-member. Both metals and sulfur were dominantly derived from porphyritic intrusions, whereas the ore-forming fluids were initially derived from the magmatic intrusions, with increasing involvement of meteoric water in time and distance from magmatic-hydrothermal center. Fluid immiscibility in the early stage and fluid mixing in the later stage, together with cooling, were responsible for ore precipitation. Based on this mineralization model, it is inferred that concealed porphyry Cu-Mo mineralization may be developed underneath the No. 3571 and Qixing.

Formation and genesis of Paleozoic sediment-hosted barite deposits in Turkey

Most barite deposits in Turkey are sediment-hosted deposits which are located in different lithologies within passive margin sediments from the Paleozoic. The Şarkikaraağaç, Hüyük and Tordere deposits occur in the western part of the Tauride-Anatolide tectonic unit, whereas the Şekeroba and Önsen region deposits located in the eastern part of Turkey occur on both Arabian and Tauride-Anatolide microplates. While the former deposits occur as both concordant and discordant bodies within Early Paleozoic carbonates, the latter deposits are found as discordant, fracture filling and replacement-type ore bodies.O, D, S, Sr and Pb isotope studies were used to determine and correlate the formation conditions of these deposits. δ18OSMOW mean values of the Tordere barite deposit are slightly higher (mean 16.2‰) than the mean values for the Şekeroba (10.8‰) and Önsen (11.3‰) deposits. The δ18OSMOW (mean 15.83‰) and δDSMOW (mean −67‰) values obtained from fluid inclusions in quartz veins in the Şekeroba barite deposit correspond to metamorphic or deep circulation hydrothermal waters. Mean δ34 SCDT values from Şekeroba, Tordere and Önsen deposits are 31.7, 33.8 and 20.6‰, respectively, which are compatible with the early Paleozoic seawater, except for the Önsen deposit.87Sr/86Sr mean values for the barite deposits of Turkey are defined as follows (‰); Şekeroba: 0.713, Önsen: 0.711, and Tordere: 0.711, which are higher 87Sr/86Sr isotope ratios than Paleozoic seawater. The Pb isotope values in Şekeroba and Tordere deposits are similar and mean is 206Pb/204Pb = 18.28, 207Pb/204Pb = 15.67 and 208Pb/204Pb = 38.50. High radiogenic Sr and Pb isotope data from the deposits indicate that Ba was generated from thick Paleozoic clastics or the older crust beneath them.Sr, S, and O isotopes and the positive Gd anomaly in the barites are very similar to those of Paleozoic stratiform cold-seep barites. The primary stratiform-stratabound barite deposits, like Şarkikaraağaç-Hüyük deposit, could have formed either by cold seep or diagenetic processes at the sediment–seawater interface or within the sediment related to sulfate-methane boundary. Although there are similar Sr and Pb isotopic signatures between the western and eastern region deposits, the eastern region Şekeroba, Önsen and Tordere barite deposits show discordant ore geometry and highly radiogenic isotope values indicating that primary stratabound-stratiform barite was dissolved and remobilized along deep-seated fault zones during the Hercynian orogenesis and deposited in different Paleozoic lithologies related to cooling and/or increase in Eh.

Trace elemental and sulfur-lead isotopic variations in metamorphosed volcanogenic massive sulfide (VMS) mineralization systems: An example from the Keketale Pb-Zn(-Ag) deposit, NW China

The effects of post-VMS (volcanogenic massive sulfide) deformation/metamorphism on sulfide trace element and sulfur-lead isotopic compositions remain unclear. The greenschist to lower amphibolite facies metamorphosed Keketale VMS Pb-Zn(-Ag) deposit, located in the Devonian Maizi volcanic-sedimentary basin in the Chinese Altay, NW China, provides an opportunity to resolve the abovementioned issue. Two mineralization stages are recognized at Keketale, including (1) primary banded, massive and disseminated ores derived from sea-floor hydrothermal mineralization and (2) ore remobilization, as represented by intensively-deformed ores and quartz-polymetallic sulfide ore veins that crosscut the primary ores. Sulfide trace elements data suggest that Stage II pyrite and pyrrhotite have higher contents of Cu, Zn, Ag, Sb and Pb, whereas contents of these elements are higher in Stage I sphalerite and galena than their Stage II counterparts. Such elemental remobilization was probably caused by the rapid intragrain diffusion and subsequent fluid-mediated liberation with trace elements re-precipitated as particles within the same grain and nearby minerals, respectively. The δ34SCDT values in both stages show a trimodal distribution (−25.9 to −22.7‰, −17.0 to −10.6‰ and 0.6 to 2.1‰). Sulfide mineral pairs formed during primary VMS mineralization are not in sulfur isotopic equilibrium, and only localized re-equilibration occurs during deformation and metamorphism. In addition, the lead isotopic values of galena from remobilized sulfide veins overlap with those of the Stage I galena and pyrite. These data indicate that regional deformation and metamorphism of the Keketale deposit can be approximated as a closed system in terms of sulfur-lead isotopes. Whilst the presence of the anomalously low δ34S values (minimum −25.9‰) and the distinct lead isotopic ratios of sulfides from the calcite-quartz veins argue for that in the late part of the metamorphic event, some exotic lead and light sulfur were sourced from outside the ore field. In situ δ34S values of Stage I sulfides vary widely (−17.0 to +2.1‰), suggesting that the sulfur was originated from bacterial sulfate reduction (BSR) of marine sulfates with probably some magmatic input. Lead isotopes of the sulfides and mineralized meta-sedimentary-volcanic rocks display a linear distribution between the mantle and upper crust line in the 206Pb/204Pb vs. 207Pb/204Pb diagram. The lead source may be derived from both felsic volcanic rocks and mafic igneous rocks (and/or magmatic volatiles), and the sulfur-lead isotopes may result from a shallow-level seawater circulating process. An additional group of lead isotopic compositions of the meta-volcanic rocks show elevated present-day 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb values, probably due to decay of Th and U carried by deeply-penetrative circulation (~13 km) of CO2-F-Cl-rich hydrothermal (metamorphic) fluids. Both syn-VMS shallow (seawater) and post-VMS deep (metamorphic fluids) circulation processes are critical for the metal concentration at Keketale.

The origin of Miocene evaporites in the Tuz Gölü basin (Central Anatolia, Turkey): Implications from strontium, sulfur and oxygen isotopic compositions of the Ca-Sulfate minerals

Sulfur, oxygen and strontium isotope compositions of the sulfate minerals (gypsum and anhydride) of the Miocene evaporites in the Tuz Gölü basin which is the largest, closed and inner basin of Turkey located in the Central Anatolia, were investigated to evaluate the origin of the sulfates and interpret the precipitation paleoenvironment. The isotopic, mineralogical and chemical properties and composition of the samples collected from drillings were investigated. The δ34SCDT and δ18OSMOW values of the sulfate minerals range from 18.78 to 35.90‰ and 7.55–22.57‰, respectively. Most of the δ34S values are similar to marine (Messinian) water. In addition, the 87Sr/86Sr ratios of the minerals vary from 0.707803 to 0.708209.Most of the δ34S and δ18O values and 87Sr/86Sr ratios of the investigated samples in the Tuz Gölü basin are similar to those of the isotopic values of the Messinian marine sulfates indicating that the minerals were precipitated mostly from marine water. The 34S and 18O values of some samples are higher than those of the evaporites precipitated from the Miocene seawater and indicate that the evolution of the sufates in the basin was also controlled by the recycling-dissolution of the predeposited marine sulfates (Oligocene-Eocene), arid conditions and bacterial sulfate reduction (BSR) processes. Additionally, the low δ18O values and 87Sr/86Sr ratios with high Sr content of some samples other than those of the Miocene marine sulfates may have been caused by the influence of volcanic emanations, hydrothermal fluid, re-oxidation of sulfur and partially the contribution of the external or internal nonmarine water to the basin (e.g., meteoric water or groundwater/surface water). The Ca-sulfate minerals with high Sr contents and low 87Sr/86Sr ratios may have precipitated under the seawater-dominated hydrothermal fluid mixing conditions.