Re–Os and U–Pb Geochronology of the Dawan Mo–Zn–Fe Deposit in Northern Taihang Mountains,China

The Dawan Mo–Zn–Fe deposit located in the Northern Taihang Mountains in the middle of the North China Craton (NCC) contains large Mo‐dominant deposits. The mineralization of the Dawan Mo–Zn–Fe deposit is associated with the Mesozoic Wanganzhen granitoid complex and is mainly hosted within Archean metamorphic rocks and Proterozoic–Paleozoic dolomites. Rhyolite porphyry and quartz monzonite both occur in the ore field and potassic alteration, strong silicic–phyllic alteration, and propylitic alteration occur from the center of the rhyolite porphyry outward. The Mo mineralization is spacially related to silicic and potassic alteration. The Fe orebody is mainly found in serpentinized skarn in the external contact zone between the quartz monzonite and dolomite. Six samples of molybdenite were collected for Re–Os dating. Results show that the Re–Os model ages range from 136.2 Ma to 138.1 Ma with an isochron age of 138 ± 2 Ma (MSWD = 1.2). U–Pb zircon ages determined by laser ablation inductively coupled plasma mass spectrometry yield crystallization ages of 141.2 ± 0.7 (MSWD = 0.38) and 130.7 ± 0.6 Ma (MSWD = 0.73) for the rhyolite porphyry and quartz monzonite, respectively. The ore‐bearing rhyolite porphyry shows higher K₂O/Na₂O ratios, ranging from 58.0 to 68.7 (wt%), than those of quartz monzonite. All of the rock samples are classified in the shoshonitic series and characterized by enrichment in large ion lithophile elements; depletion in Mg, Fe, Ta, Ni, P, and Y; enrichment in light rare earth elements with high (La/Yb)_n ratios. Geochronology results indicate that skarn‐type Fe mineralization associated with quartz monzonite (130.7 ± 0.6 Ma) formed eight million years later than Mo and Zn mineralization (138 ± 2 Ma) in the Dawan deposit. From Re concentrations in molybdenite and previously presented Pb and S isotope data, we conclude that the ore‐forming material of the deposit was derived from a crust‐mantle mixed source. The porphyry‐skarn type Cu–Mo–Zn mineralization around the Wanganzhen complex is related to the primary magmatic activity, and the skarn‐type Fe mineralization is formed at the late period magmatism. The Dawan Mo–Zn–Fe porphyry‐skarn ores are related to the magmatism that was associated with lithospheric thinning in the NCC.     

Ore Genesis for Stratiform Ore Bodies of the Dongfengnanshan Copper Polymetallic Deposit in the Yanbian Area, NE China：Constraints from LA-ICP-MS in situ Trace Elements and Sulfide S–Pb Isotopes

The Dongfengnanshan Cu polymetallic deposit is one representative deposit of the Tianbaoshan ore district in the Yanbian area, northeast(NE) China. There occur two types of ore bodies in this deposit, the stratiform ore bodies and veintype ones, controlled by the Early Permian strata and the Late Hercynian diorite intrusion, respectively. Due to the ambiguous genetic type of the stratiform ore bodies, there has been controversy on the relationship between them and veintype ore bodies. To determine the genetic type of stratiform ore bodies, laser ablation inductively coupled plasma mass spectrometry(LA-ICP-MS) in situ trace elements and S–Pb isotope analysis have been carried on the sulfides in the stratiform ore bodies. Compared with that in skarn, Mississippi Valley-type(MVT), and epithermal deposits, sphalerite samples in the stratiform ore bodies of the Dongfengnanshan deposit are significantly enriched in Fe, Mn, and In, while depleted in Ga, Ge, and Cd, which is similar to the sphalerite in volcanic-associated massive sulfide(VMS) deposits. Co/Ni ratio of pyrrhotites in the stratiform ore bodies is similar to that in VMS-type deposits. The concentrations of Zn and Cd of chalcopyrites are similar to those of recrystallized VMS-type deposits. These characteristics also reflect the intermediate ore-forming temperature of the stratiform ore bodies in this deposit. Sulfur isotope compositions of sulfides are similar to those of VMS-type deposits, reflecting that sulfur originated from the Permian Miaoling Formation. Lead isotope compositions indicate mixed-source for lead. Moreover, the comparison of the Dongfengnanshan stratiform ore bodies with some VMStype deposits in China and abroad, on the trace elements and S–Pb isotope characteristics of the sulfides reveals that the stratiform ore bodies of the Dongfengnanshan deposit belong to the VMS-type, and have closely genetic relationship with the early Permian marine volcanic sedimentary rocks.     

Geochronology and Ore‐Forming Fluids of the Baizhangyan W–Mo Deposit in the Chizhou Area,Middle‐Lower Yangtze Valley,SE‐China

The Baizhangyan skarn‐porphyry type W–Mo deposit is located in a newly defined Mo–W–Pb–Zn metallogenic belt, which is in the south of Middle‐Lower Yangtze Valley Cu–Fe–Au polymetallic metallogenic belt in SE China. The W–Mo orebodies occur mainly within the contact zone between fine‐grained granite and Sinian limestone strata. There are two types of W–Mo mineralization: major skarn W–Mo mineralization and minor granite‐hosted disseminated Mo mineralization which was traced by drilling at depth. Eight molybdenite samples from Mo‐bearing ores yield Re–Os dates that overlap within analytical error, with a weighted average age of 134.1 ± 2.2 Ma. These dates are in close agreement with SIMS U–Pb concordant zircon age for fine‐grained granite at 133.3 ± 1.3 Ma, indicating that crystallization of the granite and hydrothermal molybdenite formation were coeval and likely cogenetic. The Baizhangyan W–Mo deposit formed in the Early Cretaceous extensional tectonic setting at the Middle‐Lower Yangtze Valley metallogenic belt and the Jaingnan Ancient Continent. Based on mineral compositions and crosscutting relationships of veinlets, hydrothermal alteration and mineralization, the ore mineral paragenesis of the Baizhangyan deposit is divided into four stages: skarn stage (I), oxide stage (II), sulfide stage (III), and carbonate stage (IV). Fluid inclusions in garnet, scheelite, quartz and calcite from W–Mo ores are mainly aqueous‐rich (L + V) type inclusions. Following garnet deposition at stage I, the high‐temperature fluids gave way to progressively cooler, more dilute fluids associated with tungsten–molybdenite–base metal sulfide deposition (stage II and stage III) (162–360°C, 2.7–13.2 wt % NaCl equivalent) and carbonate deposition (stage IV) (137–190°C, 0.9–5 wt % NaCl equiv.). Hydrogen‐oxygen isotope data from minerals of different stages suggest that the ore‐forming fluids consisted of magmatic water, mixed in various proportions with meteoric water. From stage I to stage IV, there is a systematic decrease in the homogenization temperature of the fluid‐inclusion fluids and calculated δ¹⁸O values of the fluids. These suggest that increasing involvement of formation water or meteoric water during the fluid ascent resulted in successive deposition of scheelite and molybdenite at Baizhangyan.     

Fluid Inclusions,C–H–O–S Isotope and Geochronology of the Bujinhei Pb–Zn Deposit in the Southern Great Xing'an Range of Northeast China: Implication for Ore Genesis

The Bujinhei Pb–Zn deposit is located in the southern Great Xing'an Range metallogenic belt. It is a representative medium‐ to high‐temperature hydrothermal vein type deposit controlled by fractures, and orebodies hosted in the Permian Shoushangou Formation. The hydrothermal mineralization is classified into three stages: pyrite ± arsenopyrite–quartz (Stage 1), polymetallic sulfide–quartz (Stage 2), and polymetallic sulfide–calcite (Stage 3). Fluid inclusion petrography, laser Raman analyses and microthermometry indicate that the liquid‐rich aqueous inclusions (L) and vapor‐rich CO₂ ± CH₄–H₂O inclusions (C) occur in the Stage 1 and as medium‐ to high‐ temperature and low‐ to medium‐salinity NaCl–H₂O–CO₂–CH₄ hydrothermal fluids. The liquid‐rich (L) and rare vapor‐rich CO₂ ± CH₄–H₂O inclusions (C) occur in the Stage 2 with medium‐temperature and low‐salinity NaCl–H₂O ± CO₂ ± CH₄ hydrothermal fluids. The exclusively liquid‐rich (L) fluid inclusions are observed in the Stage 3, and the hydrothermal fluid belongs to medium‐temperature and low‐salinity NaCl–H₂O hydrothermal fluids. The results of hydrogen and oxygen isotope analyses indicate that ore‐forming fluids were initially derived from the magmatic water and mixed with local meteoric water in the late stage (δ¹⁸O_H2O‐SMOW = 6.0 to 2.2‰, δD_SMOW = ?103 to ?134‰). The carbon isotope compositions (?18.4‰ to ?26.5‰) indicate that the carbon in the fluid was derived from the surrounding strata. The sulfur isotope compositions (5.7 to 15.2‰) indicate that the ore sulfur was also primarily derived from the strata. The ore vein No. 1 occurs in fractures and approximately parallel to the rhyolite porphyry; orebodies have a close spatial and temporal relationship with the rhyolite porphyry. The rhyolite porphyry yielded a crystallization age of 122.9  ± 2.4 Ma, indicating that the Bujinhei deposit may be related to the Early Cretaceous magmatic event. Geochemical analyses reveal that the Bujinhei rhyolite porphyry is high in K₂O and peraluminous, and derived from an acidic liquid as a result of strong interaction with hydrothermal fluid during the late magmatic stage; it is similar to A2‐type granites, and formed in a backarc extensional environment. These results indicate that the Bujinhei Pb–Zn deposit was a vein type system that formed in Early Cretaceous and influenced by the Paleo‐Pacific tectonic system. Bujinhei deposit is a representative hydrothermal vein type deposit on the genetic types, and occurs on the western slope of the southern Great Xing'an Range. The ore‐forming fluids were medium‐ to high‐temperature and low‐to medium‐salinity NaCl–H₂O–CO₂–CH₄ hydrothermal fluids, which became medium‐temperature and low‐salinity NaCl–H₂O hydrothermal fluids in later stages, and came from magmatic water and mixed with meteoric water, whereas the ore‐forming materials were mainly derived from the surrounding strata. The LA–ICP–MS zircon U–Pb dating indicates that the Bujinhei deposit formed at the period of late Early Cretaceous, potentially in a backarc extensional environment influenced by the Paleo‐Pacific tectonic system.     

Petrogenesis of the Yangchang Mo‐bearing granite in the Xilamulun metallogenic belt,NE China: geochemistry,zircon U–Pb ages and Sr–Nd–Pb isotopes

The Yangchang granite‐hosted Mo deposit is typical of the Xilamulun metallogenic belt, which is one of the important Mo–Pb–Zn–Ag producers in China. A combination of major and trace element, Sr, Nd and Pb isotope, and zircon U–Pb age data are reported for the Yangchang batholith to constrain its petrogenesis and Mo mineralization. Zircon LA‐ICPMS U–Pb dating yields mean ages of 138 ± 2 and 132 ± 2 Ma for monzogranite and granite porphyry, respectively. The monzogranites and granite porphyries are calc‐alkaline with K₂O/Na₂O ratios of 0.75–0.92 and 1.75–4.42, respectively. They are all enriched in large‐ion lithophile elements (LILEs) and depleted in high‐field‐strength elements (HFSEs) with negative Nb and Ta anomalies in primitive‐mantle‐normalized trace element diagrams. The monzogranites have relatively high Sr (380–499 ppm) and Y (14–18 ppm) concentrations, and the granite porphyries have lower Sr (31–71 ppm) and Y (5–11 ppm) concentrations than those of monzogranites. The monzogranites and granite porphyries have relatively low initial Sr isotope ratios of 0.704573–0.705627 and 0.704281, respectively, and similar ²⁰⁶Pb/²⁰⁴Pb ratios of 18.75–18.98 and 18.48–18.71, respectively. In contrast, the ε_Nd(t) value (−3.7) of granite porphyry is lower than those of monzogranites (−1.5 to −2.7) with Nd model ages of about 1.0 Ga. These geochemical features suggest that the monzogranite and granite porphyries were derived from juvenile crustal rocks related to subduction of the Paleo‐Pacific plate under east China. Copyright © 2013 John Wiley & Sons, Ltd.     

Genesis of the Changba–Lijiagou Giant Pb-Zn Deposit, West Qinling, Central China: Constraints from S-Pb-C-O isotopes

The extensive Changba-Lijiagou Pb-Zn deposit is located in the north of the Xihe–Chengxian ore cluster in West Qinling. The ore bodies are mainly hosted in the marble, dolomitic marble and biotite-calcite-quartz schist of the Middle Devonian Anjiacha Formation, and are structurally controlled by the fault and anticline. The ore-forming process can be divided into three main stages, based on field geological features and mineral assemblages. The mineral assemblages of hydrothermal stage I are pale-yellow coarse grain, low Fe sphalerite, pyrite with pits, barite and biotite. The mineral assemblages of hydrothermal stage II are black-brown cryptocrystalline, high Fe shalerite, pyrite without pits, marcasite or arsenopyrite replace the pyrite with pits, K-feldspar. The features of hydrothermal stage III are calcite-quartz-sulfide vein cutting the laminated, banded ore body. Forty-two sulfur isotope analyses, twenty-five lead isotope analyses and nineteen carbon and oxygen isotope analyses were determined on sphalerite, pyrite, galena and calcite. The δ34 S values of stage I(20.3 to 29.0‰) are consistent with the δ34 S of sulfate(barite) in the stratum. Combined with geological feature, inclusion characteristics and EPMA data, we propose that TSR has played a key role in the formation of the sulfides in stage I. The δ34 S values of stage II sphalerite and pyrite(15.1 to 23.0‰) are between sulfides in the host rock, magmatic sulfur and the sulfate(barite) in the stratum. This result suggests that multiple S reservoirs were the sources for S2-in stage II. The δ34 S values of stage III(13.1 to 22‰) combined with the structure of the geological and mineral features suggest a magmatic hydrothermal origin of the mineralization. The lead isotope compositions of the sulfides have 206 Pb/204 Pb ranging from 17.9480 to 17.9782, 207 Pb/204 Pb ranging from 15.611 to 15.622, and 208 Pb/204 Pb ranging from 38.1368 to 38.1691 in the three ore-forming stages. The narrow and symmetric distributions of the lead isotope values reflect homogenization of granite and mantle sources before the Pb-Zn mineralization. The δ13 CPDB and δ18 OSMOW values of stage I range from-0.1 to 2.4‰ and from 18.8 to 21.7‰. The values and inclusion data indicate that the source of fluids in stage I was the dissolution of marine carbonate. The δ13 CPDB and δ18 OSMOW values of stage II range from-4 to 1‰ and from 12.3 to 20.3‰, suggesting multiple C-O reservoirs in the Changba deposit and the addition of mantle-source fluid to the system. The values in stage III are-3.1‰ and 19.7‰, respectively. We infer that the process of mineralization involved evaporitic salt and sedimentary organic-bearing units interacting through thermochemical sulfate reduction through the isotopic, mineralogy and inclusion evidences. Subsequently, the geology feature, mineral assemblages, EPMA data and isotopic values support the conclusion that the ore-forming hydrothermal fluids were mixed with magmatic hydrothermal fluids and forming the massive dark sphalerite, then yielding the calcite-quartz-sulfide vein ore type at the last stage. The genesis of this ore deposit was epigenetic rather than the previously-proposed sedimentary-exhalative(SEDEX) type.     

Two Periods of Skarn Mineralization in the Baizhangyan W–Mo Deposit,Southern Anhui Province,Southeast China: Evidence from Zircon U–Pb and Molybdenite Re–Os and Sulfur Isotope Data

The recently discovered Baizhangyan skarn‐porphyry type W–Mo deposit in southern Anhui Province in SE China occurs near the Middle–Lower Yangtze Valley polymetallic metallogenic belt. The deposit is closely temporally‐spatially associated with the Mesozoic Qingyang granitic complex composed of g ranodiorite, monzonitic g ranite, and alkaline g ranite. Orebodies of the deposit occur as horizons, veins, and lenses within the limestones of Sinian Lantian Formation contacting with buried fine‐grained granite, and diorite dykes. There are two types of W mineralization: major skarn W–Mo mineralization and minor granite‐hosted disseminated Mo mineralization. Among skarn mineralization, mineral assemblages and cross‐cutting relationships within both skarn ores and intrusions reveal two distinct periods of mineralization, i.e. the first W–Au period related to the intrusion of diorite dykes, and the subsequent W–Mo period related to the intrusion of the fine‐grained granite. In this paper, we report new zircon U–Pb and molybdenite Re–Os ages with the aim of constraining the relationships among the monzonitic granite, fine‐grained granite, diorite dykes, and W mineralization. Zircons of the monzonitic granite, the fine‐grained granite, and diorite dykes yield weighted mean U–Pb ages of 129.0 ± 1.2 Ma, 135.34 ± 0.92 Ma and 145.3 ± 1.7 Ma, respectively. Ten molybdenite Re–Os age determinations yield an isochron age of 136.9 ± 4.5 Ma and a weighted mean age of 135.0 ± 1.2 Ma. The molybdenites have δ³⁴S values of 3.6‰–6.6‰ and their Re contents ranging from 7.23 ppm to 15.23 ppm. A second group of two molybdenite samples yield ages of 143.8 ± 2.1 and 146.3 ± 2.0 Ma, containing Re concentrations of 50.5–50.9 ppm, and with δ³⁴S values of 1.6‰–4.8‰. The molybdenites from these two distinct groups of samples contain moderate concentrations of Re (7.23–50.48 ppm), suggesting that metals within the deposit have a mixed crust–mantle provenance. Field observation and new age and isotope data obtained in this study indicate that the first diorite dyke‐related skarn W–Au mineralization took place in the Early Cretaceous peaking at 143.0–146.3 Ma, and was associated with a mixed crust–mantle system. The second fine‐grained granite‐related skarn W–Mo mineralization took place a little later at 135.0–136.9 Ma, and was crust‐dominated. The fine‐grained granite was not formed by fractionation of the Qingyang monzonitic granite. This finding suggests that the first period of skarn W–Au mineralization in the Baizhangyan deposit resulted from interaction between basaltic magmas derived from the upper lithospheric mantle and crustal material at 143.0–146.3 and the subsequent period of W–Mo mineralization derived from the crust at 135.0–136.9 Ma.     

A study of igneous rocks related to Zn–Pb mineralization in the Shinyemi and Gagok deposits of the Taebaeksan Basin,South Korea

The Shinyemi and Gagok deposits, located in the Taebaeksan Basin, South Korea, display Zn–Pb mineralization along a contact between Cretaceous granitoids and Cambrian–Ordovician carbonates of the Joseon Supergroup. The Shinyemi mine is one of the largest polymetallic skarn‐type magnetite deposits in South Korea and comprises Fe and Fe–Mo–Zn skarns, and Zn–Cu–Pb replacement deposits. Both deposits yield similar Cretaceous mineralization ages, and granitoids associated with the two deposits displaying similar mineral textures and compositions, are highly evolved, and were emplaced at a shallow depth. They are classified as calc‐alkaline, I‐type granites (magnetite series) and were formed in a volcanic arc. Compositional variation is less in the Shinyemi granites and aplites (e.g., SiO₂ = 74.4–76.6 wt% and 74.4–75.1 wt%, respectively) than in the Gagok granites and aplites (e.g., SiO₂ = 65.6–68.0 wt% and 74.9–76.5 wt%, respectively). Furthermore, SiO₂ vs K/Rb and SiO₂ vs Rb/Sr diagrams indicate that the Shinyemi granitoids are more evolved than the Gagok granitoids. Shinyemi granitoids had been already differentiated highly in deep depth and then intruded into shallow depth, so both granite and aplite show the highly evolved similar chemical compositions. Whereas, less differentiated Gagok granitoids were separated into two phases in the last stage at shallow depth, so granite and aplite show different compositions. The amounts of granites and aplite are similar in the Shinyemi deposit, whereas the aplite appears in an amount less than the granite in the Gagok deposit. For this reason, the Shinyemi granitoids caused not only Fe enrichment during formation of the dolomite‐hosted magnesian skarn but also was associated with Mo mineralization in the Shinyemi deposit. Zn mineralization of the Gagok deposit was mainly caused by granite rather than aplite. Our data suggest that the variation in mineralization displayed by the two deposits resulted from differences in the compositions of their associated igneous intrusions.     

福建龙岩大洋-莒舟花岗岩锆石U-Pb年龄和Sr-Nd-Pb同位素特征及其地质意义

马坑铁矿是一个大型层控矽卡岩型矿床,大洋、莒舟花岗岩分布于铁矿东西两侧,与铁矿关系密切。本文利用LA-ICP-MS锆石U-Pb定年法测得莒舟花岗岩年龄为129.6±0.8Ma,MSWD=2.3,利用SHRIMP锆石U-Pb定年法测得大洋花岗岩年龄为132.6±1.3Ma,MSWD=1.3,它们都形成于早白垩世,与马坑铁矿辉钼矿Re-Os年龄(130~133Ma)一致。大洋-莒舟花岗岩具高硅、富碱、贫钙镁和高分异指数等特点,属弱过铝或准铝质花岗岩;岩石稀土元素含量较高,配分模式呈轻稀土富集并缓向右倾斜,呈明显铕负异常的"V"型展布;微量元素具有Rb、U、Th、La等元素强烈富集而Ba、Sr、P、Ti 等元素相对亏损的特点;大洋岩体的(⁸⁷Sr/⁸⁶Sr)_ⅰ值变化于0.70878~0.71349之间;ε_Nd(t)值变化于-7.2~-8.6之间,f_Sm/Nd=-0.27~0.16,t_2DM =1511~1637Ma,(²⁰⁶Pb/²⁰⁴Pb)_i=18.588~18.955,(²⁰⁷Pb/²⁰⁴Pb)_i=15.660~15.682,(²⁰⁸Pb/²⁰⁴Pb)_i=38.935~39.168,μ值介于9.54~9.59,ω值介于36. 77~38.13。岩石地球化学和同位素组成特征表明大洋-莒舟花岗岩属于高分异壳源型花岗岩,形成于岩石圈减薄的背景下。花岗岩主要来源于元古代地壳物质,有EMⅡ型富集地幔组分的参与,使花岗岩的地壳留存年龄的降低(1.51~1.63Ga)。     

Age and Tectonic Setting of Mesothermal Magmatic Hydrothermal Vein‐Type Pb–Zn–(Ag) Mineralization in the Xiaohongshilazi Deposit,Central Jilin Province,Northeast China

The Xiaohongshilazi deposit located in central Jilin Province, Northeast China, is a newly discovered and medium‐scale Pb–Zn–(Ag) deposit with ore reserves of 34,968 t Pb, 100,150 t Zn, and 158 t Ag. Two‐stage mineralization has been identified in this deposit. Stratiform volcanic‐associated massive sulfide (VMS) Pb–Zn mineralization interbedding with the marine volcanic rocks of the Late Carboniferous–Early Permian Daheshen Formation was controlled by the premineralization E–W‐trending faults. Vein‐type Pb–Zn–(Ag) mineralization occurs within or parallel to the granodiorite and diorite porphyries controlled by the major‐mineralization N–S‐trending faults that cut the stratiform mineralization and volcanic rocks. To constrain the age of vein‐type Pb–Zn–(Ag) mineralization and determine the relationship between mineralization and magmatism, we conducted LA–ICP–MS U–Pb dating on zircon from the ore‐bearing granodiorite and diorite porphyries and Rb–Sr dating on metal sulfide. Granodiorite and diorite porphyries yield zircon U–Pb weighted‐mean ²⁰⁶Pb/²³⁸U ages of 203.6 ± 1.8 Ma (Mean Standard Weighted Deviation [MSWD] = 1.8) and 225.6 ± 5.1 Ma (MSWD = 2.3), respectively. Sulfides from four vein‐type ore samples yield a Rb–Sr isochron age of 195 ± 17 Ma (MSWD = 4.0). These results indicate a temporal relationship between the granodiorite porphyry and vein‐type Pb–Zn–(Ag) mineralization. The granodiorite associated with vein‐type mineralization has high SiO₂ (68.99–70.49 wt.%) and Na₂O (3.9–4.2 wt.%; Na₂O/K₂O = 1.07–1.10) concentrations, and A/CNK values of 0.95–1.04; consequently, the intrusion is classified as a high‐K, calc‐alkaline, metaluminous I‐type granite. The granodiorite porphyry is enriched in large‐ion lithophile elements (e.g. Rb, Th, U, and K) and light REE and is depleted in high‐field‐strength elements (e.g. Nb, Ta, P, and Ti) and heavy REE, indicating that it represents a subduction‐related rock that formed at an active continental margin. Furthermore, the granodiorite porphyry has Mg# values of 31–34, indicating a lower crustal source. Based on petrological and geochemical features, we infer that the ore‐bearing granodiorite porphyry was derived from the partial melting of the lower crust. In summary, mineralization characteristics, cross‐cutting relationships, geochronological data, and regional tectonic evolution indicate that the region was the site of VMS Pb–Zn mineralization that produced stratiform orebodies within the Late Carboniferous–Early Permian marine volcanic rocks of the Daheshen Formation, followed by mesothermal magmatic hydrothermal vein‐type Pb–Zn–(Ag) mineralization associated with granodiorite porphyry induced by the initial subduction of the Paleo‐Pacific Plate beneath the Eurasia Plate during the Late Triassic–Early Jurassic.     

Geochemistry,Zircon U–Pb Analysis,and Biotite 40Ar/39Ar Geochronology of the Maoling Gold Deposit,Liaodong Rift,NE China

The Maoling gold deposit is located in the southwestern part of the Liaodong rift, NE China, and has estimated reserves of 25 t. In this paper we present the results of an investigation into the geochronology and geodynamic mechanisms of igneous activity and metallogenesis within the Maoling gold deposit. New zircon U–Pb age data, biotite ⁴⁰Ar/³⁹Ar age data, whole‐rock geochemistry, and Hf isotopic analyses are presented in order to constrain the petrogenesis and mineralization of the deposit. Zircon U–Pb dating of the Wolongquan biotite monzogranite and Maoling biotite granite yielded mean ages of 194.0 ± 1.1 Ma and 196.1 ± 1.1 Ma, respectively. All the granites are characteristically high‐K calc‐alkaline, enriched in light rare earth elements and large ion lithophile elements, and depleted in high field strength elements, which is consistent with the geochemical characteristics of arc‐type magmas. The Hf isotope characteristics indicate that the granites formed by partial melting of early Paleoproterozoic crustal material. In addition, biotite ⁴⁰Ar/³⁹Ar dating indicates that the Maoling gold deposit formed at 188.9 ± 1.2 Ma, implying that the mineralization was related to both the granite intrusions. Taking into account previous data on S–Pb–O–H isotopes and our new age data, the Maoling deposit can be classified as an intrusion‐related gold deposit. Taking into account the geology of the study area and adjacent regions, we propose that the Maoling gold deposit and its associated granitic intrusions formed in a geodynamic setting that was dominated by subduction of the Paleo‐Pacific Plate beneath the Eurasian continent.     

Geology and Isotope Geochemistry of the Dongzhongla Pb–Zn Deposit in Tibet: Implications for the Origin of the Ore‐Forming Fluids and Storage Condition of Certain Metals

As a newly discovered medium‐sized deposit (proven Pb + Zn resources of 0.23 Mt, 9.43% Pb and 8.73% Zn), the Dongzhongla skarn Pb–Zn deposit is located in the northern margin of the eastern Gangdese, central Lhasa block. Based on the geological conditions in this deposit of ore‐forming fluids, H, O, C, S, Pb, Sr, and noble gas isotopic compositions were analyzed. Results show that δ¹⁸O_SMOW of quartz and calcite ranged from −9.85 to 4.17‰, and δD_SMOW ranged from −124.7 to −99.6‰ (where SMOW is the standard mean ocean water), indicating magma fluids mixed with meteoric water in ore‐forming fluids. The δ¹³C_PDB and δ¹⁸O_SMOW values of calcite range from −1.4 to −1.1‰ and from 5.3 to 15.90‰, respectively, show compositions consistent with the carbonate limestone in the surrounding rocks, implying that the carbon was primarily sourced from the dissolution of carbonate strata in the Luobadui Formation. The ore δ³⁴S composition varied in a narrow range of 2.8 to 5.7‰, mostly between 4‰ and 5‰. The total sulfur isotopic value δ³⁴S was 4.7‰ with characteristics of magmatic sulfur. The ³He/⁴He values of pyrite and galena ranged from 0.101 to 5.7 Ra, lower than those of mantle‐derived fluids (6 ± 1 Ra), but higher than those of the crust (0.01–0.05 Ra), and therefore classified as a crust–mantle mixed source. The Pb isotopic composition for ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb, and ²⁰⁸Pb/²⁰⁴Pb values of the ores were in the ranges of 18.628–18.746, 15.698–15.802, and 39.077–39.430, respectively, consistent with the Pb isotopic composition of magmatic rocks in the deposit, classified as upper‐crust lead. The ore lead was likely sourced partially from the crustal basement of the Lhasa Terrane. The initial (⁸⁷Sr/⁸⁶Sr)_i value from five sulfide samples ranged from 0.71732 to 0.72767, and associated ore‐forming fluids were mainly sourced from the partial melting of the upper‐crust materials. Pb isotopic compositions of ore sulfides from the Dongzhongla deposit are similar to that of the Yuiguila and Mengya'a deposit, indicating that they have similar sources of metal‐rich ore‐forming solution. According to basic skarn mineralogy, the economic metals, and the origin of the ore‐forming fluids, the Dongzhongla deposit was classified as a skarn‐type Pb–Zn deposit.     

Genesis of the Weiquan Ag–Polymetallic Deposit in East Tianshan, China: Evidence from Zircon U–Pb Geochronology and C–H–O–S–Pb Isotope Systematics

The Weiquan Ag-polymetallic deposit is located on the southern margin of the Central Asian Orogenic Belt and in the western segment of the Aqishan-Yamansu arc belt in East Tianshan,northwestern China. Its orebodies, controlled by faults, occur in the lower Carboniferous volcanosedimentary rocks of the Yamansu Formation as irregular veins and lenses. Four stages of mineralization have been recognized on the basis of mineral assemblages, ore fabrics, and crosscutting relationships among the ore veins. Stage I is the skarn stage(garnet + pyroxene), Stage Ⅱ is the retrograde alteration stage(epidote + chlorite + magnetite ± hematite 士 actinolite ± quartz),Stage Ⅲ is the sulfide stage(Ag and Bi minerals + pyrite + chalcopyrite + galena + sphalerite + quartz ± calcite ± tetrahedrite),and Stage IV is the carbonate stage(quartz + calcite ± pyrite). Skarnization,silicification, carbonatization,epidotization,chloritization, sericitization, and actinolitization are the principal types of hydrothermal alteration. LAICP-MS U-Pb dating yielded ages of 326.5±4.5 and 298.5±1.5 Ma for zircons from the tuff and diorite porphyry, respectively. Given that the tuff is wall rock and that the orebodies are cut by a late diorite porphyry dike, the ages of the tuff and the diorite porphyry provide lower and upper time limits on the age of ore formation. The δ~(13)C values of the calcite samples range from-2.5‰ to 2.3‰, the δ~(18)O_(H2 O) and δD_(VSMOW) values of the sulfide stage(Stage Ⅲ) vary from 1.1‰ to 5.2‰ and-111.7‰ to-66.1‰, respectively,and the δ~(13)C, δ~(18)O_(H2 O) and δD_(V-SMOW) values of calcite in one Stage IV sample are 1.5‰,-0.3‰, and-115.6‰, respectively. Carbon, hydrogen, and oxygen isotopic compositions indicate that the ore-forming fluids evolved gradually from magmatic to meteoric sources. The δ~(34)S_(V-CDT) values of the sulfides have a large range from-6.9‰ to 1.4‰, with an average of-2.2‰, indicating a magmatic source, possibly with sedimentary contributions. The ~(206)Pb/~(204)Pb, ~(207)Pb/~(204)Pb, and ~(208)Pb/~(204)Pb ratios of the sulfides are 17.9848-18.2785,15.5188-15.6536, and 37.8125-38.4650, respectively, and one whole-rock sample at Weiquan yields~(206)Pb/~(204)Pb,~(207)Pb/~(204)Pb, and ~(208)Pb/~(204)Pb ratios of 18.2060, 15.5674, and 38.0511,respectively. Lead isotopic systems suggest that the ore-forming materials of the Weiquan deposit were derived from a mixed source involving mantle and crustal components. Based on geological features, zircon U-Pb dating, and C-H-OS-Pb isotopic data, it can be concluded that the Weiquan polymetallic deposit is a skarn type that formed in a tectonic setting spanning a period from subduction to post-collision. The ore materials were sourced from magmatic ore-forming fluids that mixed with components derived from host rocks during their ascent, and a gradual mixing with meteoric water took place in the later stages.     

Geology and Geochemistry of the Bianbianshan Au‐Ag‐Cu‐Pb‐Zn Deposit,Southern Da Hinggan Mountains,Northeastern China

The Bianbianshan deposit, the unique gold-polymetal (Au-Ag-Cu-Pb-Zn) veined deposit of the polymetal metallogenic belt of the southern segment of Da Hinggan Mountains mineral province, is located at the southern part of the Hercynian fold belt of the south segment of Da Hinggan Mountains mineral province, NE China. Ores at the Bianbianshan deposit occur within Cretaceous andesite and rhyolite in the form of gold-bearing quartz veins and veinlet groups containing native gold, electrum, pyrite, chalcopyrite, galena and sphalerite. The deposit is hosted by structurally controlled faults associated with intense hydrothermal alteration. The typical alteration assemblage is sericite + chlorite + calcite + quartz, with an inner pyrite - sericite - quartz zone and an outer seicite - chlorite - calcite - epidote zone between orebodies and wall rocks. δ34 S values of 17 sulfides from ores changing from –1.67 to +0.49‰ with average of –0.49‰, are similar to δ34 S values of magmatic or igneous sulfide sulfur. 206Pb/204Pb, 207Pb/204Pb and 208Pb/ 204Pb data of sulfide from ores range within 17.66–17.75, 15.50–15.60, and 37.64–38.00, respectively. These sulfur and lead isotope compositions imply that ore-forming materials might mainly originate from deep sources. H and O isotope study of quartz from ore-bearing veins indicate a mixed source of deep-seated magmatic water and shallower meteoric water. The ore formations resulted from a combination of hydrothermal fluid mixing and a structural setting favoring gold-polymetal deposition. Fluid mixing was possibly the key factor resulting in Au-Ag-Cu-Pb-Zn deposition in the deposit. The metallogenesis of the Bianbianshan deposit may have a relationship with the Cretaceous volcanic-subvolcanic magmatic activity, and formed during the late stage of the crust thinning of North China.     

Ore Genesis of the Lunwei Granite‐Related Scheelite Deposit in the Wuyi Metallogenic Belt,Southeast China: Constraints from Geochronology,Fluid Inclusions,and H–O–S Isotopes

A granite‐related scheelite deposit has been recently discovered in the Wuyi metallogenic belt of southeast China. The veinlet–disseminated scheelite occurs mainly in the inner and outer contact zones of the porphyritic biotite granite, spatially associated with potassic feldspathization and silicification. Re–Os dating of molybdenite intergrowths with scheelite yield a well‐constrained isochron age of 170.4 ± 1.2 Ma, coeval with the LA–MC–ICP–MS concordant zircon age of porphyritic biotite granite (167.6 ± 2.2 Ma), indicating that the Lunwei W deposit was formed in the Middle Jurassic (~170 Ma). We identify three stages of ore formation (from early to late): (I) the quartz–K‐feldspar–scheelite stage; (II) the quartz–polymetallic sulfide stage; and (III) the quartz–carbonate stage. Based on petrographic observations and microthermometric criteria, the fluid inclusions in the scheelite and quartz are determined to be mainly aqueous two‐phase (liquid‐rich and gas‐rich) fluid inclusions, with minor gas‐pure and CO₂‐bearing fluid inclusions. Ore‐forming fluids in the Lunwei W deposit show a successive decrease in temperature and salinity from Stage I to Stage III. The homogenization temperature decreases from an average of 299 °C in Stage I, through 251 °C in Stage II, to 212 °C in Stage III, with a corresponding change in salinity from an average of 5.8 wt.%, through 5.2 wt.%, to 3.4 wt.%. The ore‐forming fluids have intermediate to low temperatures and low salinities, belonging to the H₂O–NaCl ± CO₂ system. The δ¹⁸O_H2O values vary from 1.8‰ to 3.3‰, and the δD_V‐SMOW values vary from –66‰ to –76‰, suggesting that the ore‐forming fluid was primarily of magmatic water mixed with various amounts of meteoric water. Sulfur isotope compositions of sulfides (δ³⁴S ranging from –1.1‰ to +2.4‰) and Re contents in molybdenite (1.45–19.25 µg/g, mean of 8.97 µg/g) indicate that the ore‐forming materials originated mainly in the crust. The primary mechanism for mineral deposition in the Lunwei W deposit was a decrease in temperature and the mixing of magmatic and meteoric water. The Lunwei deposit can be classified as a porphyry‐type scheelite deposit and is a product of widespread tungsten mineralization in South China. We summarize the geological characteristics of typical W deposits (the Xingluokeng, Shangfang, and Lunwei deposits) in the Wuyi metallogenic belt and suggest that porphyry and skarn scheelite deposits should be considered the principal exploration targets in this area.     

Fluid Inclusions,Stable Isotopes,and Geochronology of the Haobugao Lead‐Zinc Deposit,Inner Mongolia,China

The Haobugao deposit, located in the southern segment of the Great Xing'an Range, is a famous skarn‐related Pb‐Zn‐(Cu)‐(Fe) deposit in northern China. The results of our fluid inclusion research indicate that garnets of the early stage (I skarn stage) contain three types of fluid inclusions (consistent with the Mesozoic granites): vapor‐rich inclusions (type LV, with V_H2O/(V_H2O + L_H2O) < 50 vol %, and the majority are 5–25 vol %), liquid‐rich two‐phase aqueous inclusions (type VL, with V_H2O/(V_H2O + L_H2O) > 50 vol %, the majority are 60–80 vol %), and halite‐bearing multiphase inclusions (type SL). These different types of fluid inclusions are totally homogenized at similar temperatures (around 320–420°C), indicating that the ore‐forming fluids of the early mineralization stage may belong to a boiling fluid system. The hydrothermal fluids of the middle mineralization stage (II, magnetite‐quartz) are characterized by liquid‐rich two‐phase aqueous inclusions (type VL, homogenization temperatures of 309–439°C and salinities of 9.5–14.9 wt % NaCl eqv.) that coexist with vapor‐rich inclusions (type LV, homogenization temperatures of 284–365°C and salinities of 5.2–10.4 wt % NaCl eqv.). Minerals of the late mineralization stage (III sulfide‐quartz stage and IV sulfide‐calcite stage) only contain liquid‐rich aqueous inclusions (type VL). These inclusions are totally homogenized at temperatures of 145–240°C, and the calculated salinities range from 2.0 to 12.6 wt % NaCl eqv. Therefore, the ore‐forming fluids of the late stage are NaCl‐H₂O‐type hydrothermal solutions of low to medium temperature and low salinity. The δD values and calculated δ¹⁸O_SMOW values of ore‐forming fluids of the deposit are in the range of ?4.8 to 2.65‰ and ?127.3‰ to ?144.1‰, respectively, indicating that ore‐forming fluids of the Haobugao deposit originated from the mixing of magmatic fluid and meteoric water. The S‐Pb isotopic compositions of sulfides indicate that the ore‐forming materials are mainly derived from underlying magma. Zircon grains from the mineralization‐related granite in the mining area yield a weighted ²⁰⁶Pb/²³⁸U mean age of 144.8 ±0.8 Ma, which is consistent with a molybdenite Re‐Os model age (140.3 ±3.4 Ma). Therefore, the Haobugao deposit formed in the Early Cretaceous, and it is the product of a magmatic hydrothermal system.     

Fluid Inclusions and C,H, O,S, and Pb Isotopic Compositions of the Dabaoshan Cu Polymetallic Deposit,Northern Guangdong Province,South China

The Dabaoshan deposit in Northern Guangdong Province, South China, is a Cu–Mo–W–Pb–Zn polymetallic deposit, located in the southern part of the Qin–Hang porphyry–skarn Cu–Mo ore belt. The deposit mainly comprises porphyry Mo and stratiform skarn Cu ore deposits. The genesis of the Cu ore deposit has been ascribed to a typical skarn ore deposit formed by the metasomatism of Devonian carbonate rock layers or to a volcanic rock‐hosted massive sulfide deposit formed by marine exhalation. In this paper, we report on the homogenization temperatures and salinities of fluid inclusions and C, H, O, S, and Pb isotopic compositions of fluids and minerals in this deposit. Homogenization temperatures and salinities of fluid inclusions in garnet, diopside, quartz, and calcite provide information on the skarnification, mineralization, and postmineralization stages. The data show that ore‐forming fluids experienced a continuous transition from high temperatures and salinities to low temperatures and salinities over the entire period of mineralization. C, H, and O isotopic compositions indicate that ore‐forming fluids were derived mainly from magmatic water. O isotopic compositions indicate that ore‐forming fluids mingled with atmospheric water during the last stage of mineralization. Sulfur in the ore came mainly from deep magmatic sources. Pb isotopic compositions in the orebody show that almost all the lead in the ore was derived from magma with a crustal source. Combined geological, geophysical, and geochemical data were achieved before we proposed that the Dabaoshan porphyry–skarn Cu–Mo–W–Pb–Zn deposit, as one member of the Qin–Hang porphyry–skarn Cu–Mo ore belt, formed during the Jurassic subduction of the paleo‐Pacific plate beneath the Eurasian continent at quite low angle. NE‐ and EW‐trending structures controlled the emplacement of magmatic rocks in the South China region. In the mining area, the Xiangguanping Fault and its branches were the main conduits for magmatic crystallization and mineralization. The many subfaults, folds, and interlayer fracture zones on both sides of the main fault provided the requisite space for the ore and, together, were the controlling structures of the orebody.     

Isotope geochemistry and Re–Os geochronology of the Yanjiagou Mo deposit in the central North China Craton

The Yanjiagou deposit, located in the central North China Craton (NCC), is a newly found porphyry‐type Mo deposit. The Mo mineralization here is spatially associated with the Mapeng batholith. In this study, we identify four stages of ore formation in this deposit: pyrite phyllic stage (I), quartz–pyrite stage (II), quartz–pyrite–molybdenite stage (III), which is the main mineralization stage, and quartz–carbonate stage (IV). We present sulphur and lead isotope data on pyrite, and rhenium and osmium isotopes of molybdenite from the porphyry deposit and evaluate the timing and origin of ore formation. The δ³⁴S values of the pyrite range from ‐1.1‰ to −0.6‰, with an average of −0.875‰, suggesting origin from a mixture of magmatic/mantle sources and the basement rocks. The Pb isotope compositions of the pyrite show a range of 16.369 to 17.079 for ²⁰⁶Pb/²⁰⁴Pb, 15.201 to 15.355 for ²⁰⁷Pb/²⁰⁴Pb, and 36.696 to 37.380 for ²⁰⁸Pb/²⁰⁴Pb, indicating that the ore‐forming materials were derived from a mixture of lower crust (or basement rocks) and mantle. Rhenium contents in molybdenite samples from the main ore stage are between 74.73 to 254.43 ppm, with an average of 147.9 ppm, indicating a mixed crustal‐mantle source for the metal. Eight molybdenite separates yield model ages ranging from 124.17 to 130.80 Ma and a mean model age of 128.46 Ma. An isochron age of 126.7 ± 1.1 Ma (MSWD = 2.1, initial ¹⁸⁷Os = 0.0032 ± 0.0012 ppb) is computed, which reveals a close link between the Mo mineralization and the magmatism that generated the Mapeng batholith. The age is close to the zircon U–Pb age of ca. 130 Ma from the batholith reported in a recent study. The age is also consistent with the timing of mineralization in the Fuping ore cluster in the central NCC, as well as the peak time of lithosphere thinning and destruction of the NCC. We evaluate the spatio‐temporal distribution of the Mo deposits in the NCC and identify three important molybdenum provinces along the northern and southern margins of the craton formed during three distinct episodes: Middle to Late Triassic (240–220 Ma), Early Jurassic (190–175 Ma), and Late Jurassic to Early Cretaceous (150–125 Ma). The third period is considered to mark the most important metallogenic event, coinciding with the peak of lithosphere thinning and craton destruction in the NCC. Copyright © 2014 John Wiley & Sons, Ltd.     

Geochronology and Genesis of the Tiegelongnan Porphyry Cu(Au) Deposit in Tibet: Evidence from U–Pb,Re–Os Dating and Hf,S, and H–O Isotopes

The Tiegelongnan Cu (Au) deposit is the largest copper deposit newly discovered in the Bangong–Nujiang metallogenic belt. The deposit has a clear alteration zoning consisting of, from core to margin, potassic to propylitic, superimposed by phyllic and advanced argillic alteration. The shallow part of the deposit consists of a high sulphidation‐state overprint, mainly comprising disseminated pyrite and Cu–S minerals such as bornite, covellite, digenite, and enargite. At depth porphyry‐type mineralization mainly comprises disseminated chalcopyrite, bornite, pyrite, and a minor vein molybdenite. Mineralization is disseminated and associated with veins contained within the porphyry intrusions and their surrounding rocks. The zircon U–Pb ages of the mineralized diorite porphyry and granodiorite porphyry are 123.1 ± 1.7 Ma (2σ) and 121.5 ± 1.5 Ma (2σ), respectively. The molybdenite Re–Os age is 121.2 ± 1.2 Ma, suggesting that mineralization was closely associated with magmatism. Andesite lava (zircon U–Pb age of 111.7 ± 1.6 Ma, 2σ) overlies the ore‐bodies and is the product of post‐mineralization volcanic activity that played a critical role in preserving the ore‐bodies. Values of ?4.6 ‰ to + 0.8 ‰ δ³⁴S for the metal sulfides (mean ? 1.55 ‰) suggest that S mainly has a deep magmatic source. The H and O isotopic composition is (δD = ?87 ‰ to ?64 ‰; δ¹⁸O_H2O = 5.5 ‰ to 9.0 ‰), indicating that the ore‐forming fluids are mostly magmatic‐hydrothermal, possibly mixed with a small amount of meteoric water. The zircon ε_Hf(t) of the diorite porphyry is 3.7 to 8.3, and the granodiorite porphyry is 1.8 to 7.5. Molybdenite has a high Re from 382.2 × 10^?6 to 1600 × 10^?6. Re and Hf isotope composition show that Tiegelongnan has some mantle source, maybe the juvenile lower crust from crust–mantle mixed source. Metallogenesis of the Tiegelongnan giant porphyry system was associated with intermediate to acidic magma in the Early Cretaceous (~120 Ma). The magma provenance of the Tiegelongnan deposit has some mantle‐derived composition, possibly mixed with the crust‐derived materials.     

U–Pb and Re–Os Geochronology of the Tongcun Molybdenum Deposit and Zhilingtou Gold‐Silver Deposit in Zhejiang Province,Southeast China,and Its Geological Implications

Mesozoic ore deposits in Zhejiang Province, Southeast China, are divided into the northwestern and southeastern Zhejiang metallogenic belts along the Jiangshan–Shaoxing Fault. The metal ore deposits found in these belts are epithermal Au–Ag deposits, hydrothermal‐vein Ag–Pb–Zn deposits, porphyry–skarn Mo (Fe) deposits, and vein‐type Mo deposits. There is a close spatial–temporal relationship between the Mesozoic ore deposits and Mesozoic volcanic–intrusive complexes. Zircon U–Pb dating of the ore‐related intrusive rocks and molybdenite Re–Os dating from two typical deposits (Tongcun Mo deposit and Zhilingtou Au–Ag deposit) in the two metallogenic belts show the early and late Yanshanian ages for mineralization. SIMS U–Pb data of zircons from the Tongcun Mo deposit and Zhilingtou Au–Ag deposit indicate that the host granitoids crystallized at 169.7 ± 9.7 Ma (2σ) and 113.6 ± 1 Ma (2σ), respectively. Re–Os analysis of six molybdenite samples from the Tongcun Mo deposit yields an isochron age of 163.9 ± 1.9 Ma (2σ). Re–Os analyses of five molybdenite samples from the porphyry Mo orebodies of the Zhilingtou Au‐Ag deposit yield an isochron age of 110.1 ± 1.8 Ma (2σ). Our results suggest that the metal mineralization in the Zhejiang Province, southeast China formed during at least two stages, i.e., Middle Jurassic and Early Cretaceous, coeval with the granitic magmatism.