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This study evaluates the effect of organic matter impurities on pyrite Re-Os dating, using the giant Jinding sediment-hosted Zn-Pb deposit in China as an example. The Jinding deposit is hosted in a Paleocene evaporite dome that was a hydrocarbon reservoir before mineralization. Pyrite in Jinding formed in two stages: pre-ore (py1) and syn-ore (py2). Two types of py1 are recognized, organic matter-free and organic matter-bearing. The organic matter-free py1 contains homogeneously distributed low concentrations of Re (

Many intrusions with adakite-like affinities in collisional zones have obviously higher K2O contents and K2O/Na2O ratios compared with counterparts in subduction zones. A suite of Eocene post-collisional high-K2O adakite-like intrusions, mafic microgranular enclaves, and potassic–ultrapotassic lamprophyres in the Machangqing complex are associated with the Indian–Asian collision within the western Yangtze Craton, southeastern Tibet. The potassic–ultrapotassic lamprophyres, with a zircon U–Pb age of 34·1 ± 0·2 Ma, have high K2O and MgO contents, are enriched in light rare earth elements and large ion lithophile elements, and display high Rb/Sr, and low Ba/Rb and Nb/U ratios. They show enriched isotopic compositions [i.e. (87Sr/86Sr)i = 0·7070–0·7082, εNd(t) = −3·2 to −2·8], and zircon εHf(t) values (−1·6 to +2·6). Their parental magmas are inferred to have been derived from partial melting of an enriched lithospheric mantle, metasomatized by subduction-related fluids. The adakite-like intrusions, with zircon U–Pb ages of 35·4 ± 0·4 and 35·2 ± 0·3 Ma, are characterized by high SiO2 (68·8–71·1 wt%) and Al2O3 (14·0–15·3 wt%) contents, high Sr/Y (41–118) ratios, and low Y (5·3–14·7 ppm) contents. They show low contents of compatible elements (e.g. Ni = 9·5–36·2 ppm) and total REE, and lower Mg# values than the lamprophyres and mafic microgranular enclaves. The adakite-like intrusions have positive large ion lithophile element anomalies, especially potassium, negative high field strength element anomalies, negative εNd(t) (−5·5 to −3·3), and high (87Sr/86Sr)i (0·7064–0·7070) and zircon εHf(t) values (0·0 to +2·7), indicating that they were formed by partial melting of the juvenile lower crust. Mafic microgranular enclaves hosted in the adakite-like intrusions, with U–Pb ages similar to the lamprophyre of c. 34 Ma, exhibit disequilibrium textures, and some of them contain phlogopite. They exhibit potassic–ultrapotassic affinity, and relatively high compatible element contents. They are also characterized by enriched isotopic compositions with (87Sr/86Sr)i = 0·7063–0·7074, εNd(t) = −6·6 to −4·1, and variable zircon εHf(t) values (−0·6 to +3·2). Petrological and geochemical evidence suggests that the mafic microgranular enclaves were formed by magma mixing between potassic–ultrapotassic and pristine adakite-like melts. We propose a magma mixing model for the origin of the high-K2O adakite-like intrusions from the Machangqing complex. In this model, the formation of high-K2O adakite-like intrusions occurred in three stages: (1) partial melting of metasomatized lithospheric mantle generated potassic–ultrapotassic mafic melts; (2) underplating of these mafic melts beneath thickened juvenile lower crust resulted in partial melting of juvenile mafic lower crust and the generation of adakite-like melts; (3) magma mixing involved 80 % pristine adakite-like melts and 20 % potassic–ultrapotassic melts. This leads to the enrichment of K2O in these adakite-like intrusions, and magma differentiation further promotes K2O enrichment. These results are applicable to compositionally similar adakite-like rocks produced in other collisional zones, such as the Tibet, Sulu–Dabie and Zagros orogenic belts. From which we conclude that in continental collision zones, the post-collisional mantle-derived magmas characterized by potassic–ultrapotassic affinities are spatially associated with coeval collision-related adakite-like intrusions that originated from lower crustal melting. The emplacement of adakite-like and potassic–ultrapotassic rocks is controlled by the same fault systems, which increases the possibility of interaction between these two magma suites.

The Tethyan domain from China to Iran hosts many important sediment-hosted Pb–Zn deposits but most have been poorly documented. This study summarizes the salient features of these deposits and discusses the type of ore, tectonic setting, and important ore controls, on the basis of new geological observations and previous publications. The Tethyan domain is characterized by the young and extensive Himalayan–Tibetan and Zagros orogens that formed through collisions between the India/Arabia and Eurasia continents since the Late Cretaceous or early Cenozoic. Abundant Mississippi Valley-type (MVT) and subordinate clastic-dominated (CD, also known as SEDEX) Pb–Zn deposits occur in this domain, including in central and eastern Himalayan–Tibetan orogen in China, the Indian passive margin in southern Pakistan, and various tectonic units of Iran. Economically important deposits contain 0.1–21 Mt Pb + Zn and have total metal resources of ~75 Mt with ~48% being oxidized ores. All major deposits known in this domain are MVTs (i.e., the Jinding, Huoshaoyun, Mehdiabad, and Angouran deposits). Mississippi Valley-type Pb–Zn deposits occur in continental-collision-related fold-and-thrust belts and forelands, where deposits are mostly located on the margin of the Eurasian continent, with some in the Indian and Arabian continental margins. Clastic-dominated Pb–Zn deposits occur in central Iran and southern Pakistan, hosted by deep-water siliciclastic sequences of the early Cambrian rifted continental margin of Gondwana and the Jurassic passive continental margin of India, respectively. The youngest mineralized rocks and ages constrain that some important MVT deposits (e.g., the Jinding, Chaqupacha, and Angouran deposits) were formed after a main phase of regional compression, during a regional, large-scale strike-slip or crustal-extension stage in a continental collision setting. In sense of lithologic structure, important ore controls for MVT deposits include evaporite diapir structure, carbonate/evaporite dissolution–collapse structure, pre-existing barite, and porous dolostone. Much of the primary sulfide ore in this domain has been oxidized by supergene processes. This is particularly pronounced in the newly discovered Huoshaoyun deposit, where almost all sulfides have been oxidized to smithsonite and cerussite. An understanding of tectonic setting, ore controls, and supergene processes is essential in exploring for MVT deposits in this domain.

The Shimensi tungsten polymetallic deposit, situated in the Dahutang ore field, South China, is one of the largest tungsten deposits in the world, with an estimated WO3 reserve of 0.74 million tons. Coarse-grained porphyritic biotite granite (CPBG), fine-grained porphyritic biotite granite (FPBG), fine-grained biotite granite (FBG) and biotite granite porphyry (BGP) are all ore-related, but their diagenetic relationships and contributions to W-Cu-Mo mineralization are still in dispute. LA-ICP-MS monazite U-Pb dating of the CPBG, FPBG, FBG and BGP yield emplacement ages of 147.9 ± 1.1 Ma, 146.4 ± 1.1 Ma, 138.6 ± 0.98 Ma and 142.8 ± 1.7 Ma, respectively. Whole-rock geochemical results indicate that the four granites should be classified as S-type granites, but BGP has distinct features transitional between S- and I-type granites. They were possibly generated by partial melting of upper crustal pelites and basic volcanic rocks with different proportion from the Neoproterozoic Shuangqiaoshan Group in the source. Proportional variation in the magmatic source (clay and basic basalts) induces the change of geochemical compositions of the Shimensi granites. Geochemical characteristics suggest that they were derived from two magma chambers (the CPBG, FPBG and FBG vs. the BGP) and experienced different evolutionary processes and different degree of magmatic differentiation during magmatic evolution. Chondrite-normalized REE patterns for the four granites display low total REE contents, variable and strongly enriched LREE relative to HREE and medium-strong negative Eu anomalies. They are enriched in Rb, Th, U, Ta and depleted in Ba, Nb, Sr, P, Ti. Biotites are iron-rich and aluminum-poor, and can be classified as ferro-biotite (CPBG, FPBG and FBG) and siderophyllite (BGP). The partial melting of tungsten-rich metasediments of the Shuangqiaoshan Group and high degree of fractional crystallization led to enrichment in tungsten in the magma suites. Oxygen fugacities of the CPBG and FPBG declined from early (most above the NNO buffers) to late stages of fractional crystallization (between the NNO and QFM buffers) because of the higher degree of magmatic differentiation in the late stages. In the early stages of fractionation, tungsten accumulated in the residual melts rather than partitioning into accessory minerals. In the late stages, lower oxygen fugacities and high fluorine contents promoted the removal of tungsten from the residual magma into reduced hydrothermal fluids. On the other hand, the FBG and BGP remained constant (above the NNO buffers) over the entire process of crystallization owning to the stable degree of magmatic differentiation, promoting retention of tungsten in the melt and resulting in low grade tungsten mineralization. Tungsten mineralization in the Shimensi deposit is greatly controlled by the redox states of the associated magma. The two porphyritic granites (the CPBG and FPBG) are most likely the main contributors of tungsten, while the FBG and BGP are mainly responsible for copper and molybdenum in the Shimensi deposit. Prolonged multiphase magmatism and prolonged W-Cu-Mo mineralization play important roles in the formation of Shimensi large tungsten polymetallic deposit.

The Angouran deposit is the second-largest Zn–Pb deposit in Iran with 4.7 Mt sulfide ore (27.7% Zn, 2.4% Pb, and 110 g/t Ag) and 14.6 Mt nonsulfide ore (28.1% Zn, 4.4% Pb). Various models have been proposed to explain the genesis of sulfide ore in this deposit. Moreover, the mineralization type of its primary sulfide ores remains controversial. The major and trace element concentrations and sulfur isotopic composition of the two stages of sphalerite have been analyzed to constrain mineralization conditions and the genesis. The Angouran deposit, which contains discordant orebodies, is hosted in a Neoproterozoic/Cambrian schist-marble sequence. Two stages of sphalerite have been distinguished: early-stage (S1) red-brown sphalerite and late-stage (S2) honey-yellow sphalerite. Our result shows that, relative to the S2 sphalerite, the S1 sphalerite has higher contents of Fe, Mn, Co, Cu, Ag, Sn, Ga, Sb and In, but lower contents of As and Tl. Time-resolved depth profiles in these sphalerites determined by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) analyses indicate that Fe, Cd, Co, Hg, Mn, Ge, and In are mainly present in solid solution and that Ag, Cu, Pb, As, Ni, Ga, Tl, Sb, and Sn are present in both solid solution and mineral inclusions. Correlation analyses reveal the occurrence of direct substitution mechanisms, such as Zn2+ ↔ (Fe2+, Cd2+) and 2Zn2+ ↔ Ge4++□ (vacancy) as well as coupled substitutions, such as 2Zn2+ ↔ Cu+ + Ga3+, 2Zn2+ ↔ (Cu+, Ag+) + Sb3+, 3Zn2+ ↔ Pb2+ + Tl+ + As3+, 4Zn2+ ↔ Pb2+ + 2As3++□(vacancy) or (Zn2+, Pb2+) ↔ Tl+ + As3+, and 4Zn2+ ↔ Cu+ + (Ga3+, In3+) + Sn4++□(vacancy). Geothermometer studies suggest that sphalerite in the Angouran deposit precipitated from a low-temperature (

The world-class Dahutang tungsten deposit is located within the Jiuling mining district of the central Jiangnan orogenic belt, Jiangxi Province, China. The deposit consists of a massive and gently dipping scheelite orebody that contains disseminated and veinlet-hosted mineralization located within a medium- to coarse-grained biotite granodiorite. The No. 1 ore block of the deposit also contains a 1.50–1.75 m thick shell-shaped pegmatoid zone that defines an inner contact zone between the mineralization-related porphyritic-like biotite granite and strongly mineralized biotite granodiorite that hosts the tungsten deposit. This pegmatoid zone contains very low concentrations of tungsten, but records the processes involved in the migration and enrichment of this element within the deposit. The pegmatoid contrasts with typical hydrothermal pegmatite-type ore in that it often contains megacrystic to giant alkali feldspar, quartz, and muscovite, and is spatially zoned in terms of unique texture and composition. The pegmatoid is zoned from a felsic aplite zone with a layered texture proximal to the intrusion through quartz–feldspar pegmatoid and feldspar–quartz pegmatoid zones to a final distal quartz-dominated zone. The quartz–feldspar pegmatoid is striped and contains megacrystic feldspars that have grown nearly perpendicular to the edge of the pegmatoid, indicating the direction of movement of early exsolved magmatic fluids. Cathodoluminescence imaging indicates that there are five types of quartz within the feldspar–quartz pegmatoid: megacrystic, large phenocrystic, small phenocrystic, matrix, and vein-hosted quartz. Each of these generations of quartz crystallized early, with the disseminated metasomatic quartz that crystallized during the middle stages of pegmatoid generation being followed by the uniform crystallization of late-stage, space-filling quartz. In situ oxygen isotopic and trace element analysis indicates that all of the quartz within the pegmatoid records accelerated growth, with the middle-stage disseminated metasomatic quartz associated with an increase in δ18Oquartz values, and the late-stage space-filling quartz associated with a decrease in δ18Oquartz values. All of this quartz contains elevated concentrations of alkali metals and has low Li/Al ratios (generally 10‰, reflecting the fact that the fluids that formed these minerals were of the peraluminous granite water (PGW). The trace element compositions of the samples analyzed during this study also indicate a drop in the pH of the pegmatoid-forming fluids over time. The quartz within the feldspar–quartz pegmatoid also contains melt and gas–liquid fluid inclusions, with the latter containing significant amounts of gas-phase CH4, indicating that the pegmatoid formed from low oxygen fugacity fluids. Our data indicate that the shell-shaped pegmatoid zone within the Dahutang No. 1 ore block formed from primary PGW exsolved from the hosting intrusion, with the pegmatoid recording the transition from magmatic to hydrothermal processes during the continuous but multi-stage evolution of the Dahutang deposit. The late-stage, high-temperature, water-rich, high δ18O, alkali-metal-rich, low oxygen fugacity, and acidic nature of the hydrothermal fluids that formed the deposit promoted the transportation and further deposition of tungsten.

The investigation of epigenetic carbonate-hosted Pb-Zn deposits from China and Europe in the Eastern and Western orogens of the Tethyan Domain, have provided a new perspective on the range of processes operating in this deposit class globally. However, improved metallogenic models require new constraints on the timing of mineralization throughout the Domain. To address this need, we applied Re-Os pyrite dating to the world class Irankuh Zn-Pb deposit, Iran. The Irankah deposit is located in the thrust belt of the Malayer-Esfahan Pb-Zn Metallogenic Belt (MEMB) in the Zagros Orogen, Iran. Mineralization is hosted by the Goushfil Main Fault and adjacent dolomitized limestones. The hydrothermal mineral assemblage comprises sphalerite, galena, pyrite, minor chalcopyrite and sulfosalt minerals, together with dolomite, barite and abundant quartz. Pyrite associated with main-stage sphalerite mineralization has low concentrations of 3 to 37 ng/g Re and 6 to 49 pg/g Os that are typical of low-level highly radiogenic (LLHR) sulfides. Nonetheless, vein and replacement pyrites from the Goushfil orebody yielded a 5-point isochron age of 66.5 ± 1.6 Ma that is interpreted as the main Zn-Pb mineralization age. The new mineralization age confirms an epigenetic origin for the Irankuh Zn-Pb deposit and supports an early onset for compressional deformation in the Zagros Orogen. The geochronological data support textural evidence that mineralization in veins occurred during regional compression in an active tectonic environment. Therefore the possibility that magmatic fluids and/or heat contributed to the mineralizing system should be incorporated into regional exploration models. Further work is required to test the extent to which epigenetic carbonate-hosted Pb-Zn deposits in the thrust and fold belt settings of the Central and Eastern Tethys differ from those in the Western Tethys and classic Mississippi Valley Type ore deposits.

Cenozoic high–Sr/Y shoshonites in western Yunnan, China, are spatially and temporally associated with porphyry deposits and mafic volcanic rocks that formed at a post–collisional setting. However, the petrogenesis of these rocks and the origins of the associated mineralization remain unclear. Here we present new geochemical data for the high–Sr/Y shoshonites and associated mafic microgranular enclaves (MMEs) in the Jinshajiang–Ailaoshan mineralization belt, which formed as a result of India–Asia collision during the Cenozoic. Both fertile and barren shoshonitic porphyries were emplaced during the Eocene–Oligocene (32–37 Ma) and are characterized by enrichment in large–ion lithophile elements (LILE), depletion in high field strength elements (HFSE), high K2O (4–6 wt%), Sr contents (674–1370 ppm), and low Y contents (7–18 ppm). The barren Zhanhe, Yongsheng, Songgui, and Jianchuan, and fertile Machangqing (Cu–Au–Mo mineralization) porphyry intrusions have variable zircon eHf(t) values of −6 to +9 and old TDM2 ages of 1433 to 900 Ma. However, the barren Shigu porphyry intrusion yields relatively positive zircon eHf(t) values (−4 to +8) and younger TDM2 ages (903–631 Ma). These features indicate that the Shigu intrusion was derived from late Permian juvenile lower crust, and the other high Sr/Y shoshonites were derived mainly from Neoproterozoic juvenile lower crust. Fertile and barren porphyries have variable whole–rock eNd(t) values (−5 to −0.7) and (87Sr/86Sr) i ratios (0.70595–0.70788) that are within the range of coeval mafic magmas in western Yunnan. The MMEs comprise mafic enclaves and andesitic enclaves that formed during the Eocene (34–35 Ma) and have spheroidal shapes, igneous textures and contain acicular apatites. This indicates that the MMEs are globules of coeval mafic magma that was injected into and mixed with the host shoshonitic magma. The enclaves show low TiO2 contents (0.7–0.8 wt%), high MgO (6–9 wt%), Cr (184–450 ppm) and Ni contents (98–157 ppm), positive LILE anomalies, marked negative HFSE anomalies, a narrow range of eNd(t) values (−1.2 to −0.6), and (87Sr/86Sr) i values of 0.70556–0.70635. The andesitic enclaves show adakitic geochemical affinities and have similar zircon eHf(t) values (−2.7 to +2.5) to the host porphyries, whereas, the mafic enclaves have relatively negative zircon eHf(t) values (−8.7 to +1.5), similar to enriched mantle. These evidences suggest the high−Sr/Y shoshonites were produced by partial melting of juvenile lower crust mixed with ultrapotassic or potassic mafic magmas as represented by the andesitic enclaves. The mafic enclave melts were derived from enriched mantle metasomatized by slab–derived fluids, which elevated the Mg#, Cr, Ni contents of the host porphyries at Machangqing, Zhanhe and Yongsheng. Zircon saturation temperatures (TZr) of the high–Sr/Y shoshonitic rocks range from 735 to 777 °C and indicate the shoshonites were derived mainly from water–fluxed melting of lower crust. The Manchangqing fertile intrusion had a high oxidation state (zircon Ce4+/Ce3+ = 38–180, average = 91) and was derived by mixing between juvenile lower–crustal melts and voluminous coeval lamprophyres. In contrast, the barren Jianchuan, Songgui, Shigu, Yongsheng and Zhanhe high–Sr/Y shoshonites formed by partial melting of juvenile lower crust and some mixing with mafic lavas, and are characterized by low oxygen fugacity (zircon Ce4+/Ce3+ = 0.5–77, average = 20). As such, we suggest the mafic magmas triggered water–fluxed, moderate–degree partial melting of the lower crust and caused amphibole breakdown during melting. This process could not provide enough water for the formation of porphyry Cu-Au deposits in western Yunnan, and therefore formed low–fO2, relatively low–H2O, and barren high–Sr/Y magmas. However, ultrapotassic magmas (e.g., lamprophyres) with high H2O are able to trigger intense water–fluxed, partial melting of metal–fertilized lower crust, which generated high–fO2, relatively high–H2O, fertile, high–Sr/Y shoshonitic magmas in this intracontinental setting.

A recently discovered basanite dike in the Zaolin area of Jingdezhen, South China, contains mantle xenocrysts such as kink-banded olivines, olivines + orthopyroxenes assemblage, and chromites. In addition, polymorphic carbonates of the MgCO3–FeCO3 series occur as augens, either independently or interspersed with diopside and spinel in the matrix. The rock is characterized by high Cr and Ni contents, high whole-rock Mg# values (0.66–0.72), and high Ca/Al (0.72–1.03) and TFeO/MgO (1.1–1.3) ratios and is alkali-rich with Na2O > K2O. The trace-element partition patterns are similar to those of other basanites in eastern China as well as ocean island basalts. Whole-rock geochemical analyses show depleted Sr and Nd isotopic compositions (86Sr/87Sr=0.70358–0.703853, εNd=2.52–6.73). These data indicate that the rock has experienced negligible crustal contamination, should be derived from asthenospheric mantle, or mixed by the MORB with EMI/EMII mantle and have been carbonated. The calculated T–P conditions of the melt in equilibrium with xeno-olivine are 1160–1320°C at the mantle depth. The high Cr# values of the spinel xenocrysts indicate that the lithospheric mantle under the Jingdezhen area was probably relict Proterozoic mantle. The Ar–Ar plateau age and the isochron and inverse isochron ages for the matrix of the basanite are all 44 Ma. The basanite, as well as other alkaline basalt or lamprophyre dikes in southeastern China, formed in a rifting regime during the Eocene.

Current barriers hindering data-driven discoveries in deep-time Earth (DE) include: substantial volumes of DE data are not digitized; many DE databases do not adhere to FAIR (findable, accessible, interoperable and reusable) principles; we lack a systematic knowledge graph for DE; existing DE databases are geographically heterogeneous; a significant fraction of DE data is not in open-access formats; tailored tools are needed. These challenges motivate the Deep-Time Digital Earth (DDE) program initiated by the International Union of Geological Sciences and developed in cooperation with national geological surveys, professional associations, academic institutions and scientists around the world. DDE’s mission is to build on previous research to develop a systematic DE knowledge graph, a FAIR data infrastructure that links existing databases and makes dark data visible, and tailored tools for DE data, which are universally accessible. DDE aims to harmonize DE data, share global geoscience knowledge and facilitate data-driven discovery in the understanding of Earth's evolution., Deep-time Digital Earth is to promote data-driven discovery by harmonizing deep-time Earth data and creating ‘Geological Google’.

Post-collisional ultrapotassic rocks (UPRs) in the Tibetan Plateau exhibit extreme enrichment in incompatible elements and radiogenic isotopes. Such enrichment is considered to be either inherited from a mantle source or developed during crustal evolution. In this study, to solve this debate we combined mineral textures and in situ geochemical composition of clinopyroxene phenocrysts in UPRs from southern Tibet to reveal their crustal evolution, enrichment cause and constrain metasomatism in their mantle source. Results show that the UPRs experienced an array of crustal processes, i.e., fractional crystallization, mixing, and assimilation. Fractional crystallization is indicated by decreases in Mg# and Ni and enrichment in incompatible elements (e.g. rare earth element (REE), Sr, Zr) toward the rims of normally zoned clinopyroxene phenocrysts (type-I). Magma mixing is evidenced by the presence of some clinopyroxene phenocrysts (type-II, -III) showing disequilibrium textures (e.g. reversed and overgrowth zoning), but in situ Sr isotope and trace element analysis of those disequilibrium zones indicate that late-stage recharged mafic magmas are depleted (87Sr/86Sr: 0.70659–0.71977) compared with the primitive ultrapotassic magmas (87Sr/86Sr: 0.70929–0.72553). Assimilation is revealed by the common presence of crustal xenoliths in southern Tibetan UPRs. Considering the much lower 87Sr/86Sr values (0.707759–0.709718) and incompatible element contents of these crustal xenoliths relative to their host UPRs, assimilation should have resulted in geochemical depletion of southern Tibetan UPRs rather than enrichment. The diluting impact of both assimilation and mixing is also supported by the modeling results based on the EC-E′RAχFC model combining the growth history of clinopyroxene. Trace elements ratios in clinopyroxenes also imply that the mantle source of southern Tibetan UPRs suffered an enriched and carbonatite-dominated metasomatism. Thus, we conclude that enrichment of southern Tibetan UPRs was inherited from the mantle source.

Modern collisional orogens represent the natural laboratory for the study of metallogeny in continental collision zones. The Pyrenees, Alps, Zagros and Himalaya are all associated with Neo-Tethyan subduction and represent the youngest collisional orogens on Earth. Here, we compare these four orogens in terms of their composition, architecture, tectonic evolution, and metallogenic systems. The four orogens can be divided into simple and composite types. Simple orogens are represented by the Pyrenees and the Alps, and are characterized by narrow linear shapes in plain view and symmetric structures in cross-section, are free of arc magmatism, and are associated with the Mississippi Valley Valley-type Pb-Zn and orogenic gold deposits. The mineral deposits that form in these simple collisional orogens are generally related to processes that occur in the middle and upper crust. In contrast, composite orogens, as exemplified by the Zagros-Iranian and Himalayan-Tibetan Plateaus, are associated with broad orogenic plateaus in plain view and asymmetrical structures in cross-section, record extensive arc magmatism in continental margins, and are associated with a variety of deposit types including carbonatite-related rare earth element (REE), porphyry Cu-Mo, orogenic Au, Mississippi Valley type Pb-Zn, and detachment-fault-related polymetallic deposits. Although the subduction of Neo-Tethys oceanic crust occurred before the creation of simple collisional orogens in the Pyrenees and the Alps, these areas do not show the record of continental arc magmatism. In contrast, the composite collisional orogens are associated with the development of huge continental margin arcs prior to continental subduction, and the subduction was followed by reactivation of the subduction-modified arc lithospheric material, generating the ore-forming systems in these regions.

Phanerozoic adakites typically represent modern analogues of Middle–Late Archean (3.5–2.5 Ga) tonalite–trondhjemite–granodiorite rocks (TTGs) due to their similarities in geochemical compositions. However, no Phanerozoic analogues have been reported for the Early Archean TTGs (>3.5 Ga), which are characterized by low Sr, Y and HREEs contents with low MgO and compatible elements contents, until recent years. The newfound Phanerozoic analogues have been defined as a new adakite subgroup named as “Jamaican–type adakites” (JTAs), and been regarded as the results of partial melting of subducted oceanic plateau crust. JTA–like magmas also occur in the Nuri complex, southern Tibet. We report whole–rock geochemical, Sr Nd isotopic data, zircon U Pb ages and in-situ Hf isotopic data for adakitic quartz diorites, quartz monzonites and JTA–like quartz porphyries in the Nuri complex. Zircon U Pb dating indicates that these rocks were emplaced in the Late Cretaceous at 93.5–92.1 Ma. Combined with the continuous variation trends of major and trace elements, the similarities in terms of whole–rock Sr Nd and zircon Hf isotopic compositions indicate that the three types of rocks are genetically related, while the quartz diorites should represent the relatively primitive melts. High MgO (5.00–5.41 wt%), Cr (138–159 ppm), Ni (65.9–96.8 ppm) contents and Mg# values (66–69), high e Hf (t) values (10.5–11.9), e Nd (t) values (3.7), and low ( 87 Sr/ 86 Sr) i values (0.7046–0.7050) indicate that the quartz diorites were derived from partial melting of subducted Neo–Tethyan oceanic slab, and subsequently underwent metasomatic reaction with the mantle wedge during their ascent. Quartz monzonites and JTA–like quartz porphyries were originated from quartz diorites by two stages of fractional crystallization. Low MgO and compatible elements contents of the quartz porphyries were caused by fractionation of hornblende, biotite, with minor magnetite and allanite, while low Sr contents and Sr/Y ratios were mainly controlled by plagioclase fractionation. This means that the JTA–like geochemical features of the quartz porphyries were generated by fractional crystallization from the adakites derived from partial melting of subducted slab, rather than directly derived from partial melting of subducted oceanic plateau. Therefore, various petrogenetic possibilities of the JTA–like magmas should be considered when using them as modern analogues.

The Neotethyan tectonics of the Zagros orogenic belt, SW Iran remains still hotly debated in comparing with its western counterparts. One major issue concerns the timing and nature of the Sanandaj-Sirjan magmatic-metamorphic belt (SSMB), which is made predominantly of metamorphic rocks and Jurassic to Early Cretaceous large plutonic complexes. The Alvand and Qory are two largest plutonic complexes locating in north-central and southern segments, respectively, of the SSMB. Careful LA-ICP-MS U/Pb analyses of the magmatic zircons from the Alvand plutonic complex reveal a smooth spectra, along which the concordant age increase gradually from 120 to 190 Ma; while that of Qory is step-like consisting of two stages, a Jurassic and a late Early Cretaceous ones, respectively. New geochemical data, combined with zircon Lu/Hf results suggest that (1) the Alvand granitoids mostly resulted from a long-lived, successive injection of juvenile-crust-sourced magma batches without obvious fractionation crystallization (FC); but (2) the two stages granitoids of the Qory complex both generated by FC of juvenile-crust-sourced magmas; and (3) the gabbros of the Alvand complex are geochemically of E-MORB-affinity while those of the Qory complex are typical continental arc mafic rocks. Previously published petrological and 40Ar/39Ar data have identified a broken, Jurassic to Early Cretaceous high-pressure metamorphic belt to the southwest of the SSMB, which likely represents the closed, southeastern equivalent of the northern Neotethyan Ocean, north of the Taurides-Anatolia-Armenia block. Thus, the SSMB in Iran, the Kapan belt in Caucasus, and the Serbo-Macedonian belt in northern Turkey form a huge Jurassic to Early Cretaceous continental margin arc system recording northeastwards subduction of the older Northern Neotethyan Ocean beneath Eurasia. The Albian-Cenomanian ophiolites such as Koy, Kermanshah, and Neyriz in Iran represent the eastern counterpart of the younger Southern Neotethyan Ocean, south of the Taurides-Anatolia-Armenia block. During the subduction of the Old Neotethys, an intraplate transform fault likely opened and generated a slab-window beneath the Alvand region, which provided a constant energy source to steadily heat the low crust. This model satisfactorily interprets the unusual geochronological framework and geochemistry of the Alvand complex.

The 1600 km-long Gangdese magmatic belt features extensive Paleocene–Eocene I-type intrusive rocks and coeval volcanic successions, which can be divided into Group I (~69–53 Ma), Group II (~53–49 Ma), and Group III (~49–43 Ma), corresponding to Neo-Tethyan slab rollback, Neo-Tethyan slab breakoff, and ongoing Indian-Asian collision, respectively. The magmas from these three groups show significant variations in geochemical and isotopic compositions, which provide the information of the growth of continental crust in southern Tibet. The most voluminous magmatism in the Gangdese belt occurred during ~53–49 Ma. High zircon saturation temperature (up to 800 °C) and Ti in zircon temperature (up to 980 °C) estimations suggest there is a period of thermal anomaly during ~53–49 Ma. Starting from ~53 Ma, magmas have increased K2O contents, and their zircons have decreased Th/U ratios, and Y and Yb contents. Zircons from Group II have the most heterogeneous Hf isotopic compositions (eHf(t) = −5.3 to 15.1). These are evident of ingress of asthenosphere mantle in the arc, extensive crustal melting, and magma mixing. Magma underplating during this time is the main mechanism for the growth of continental crust. With the Indian-Asian collision going on, the magmas in Group III show high Th/Y and La/Yb ratios and K2O contents, but significantly low Tzr and T(ti-zr) values (mostly below 750 °C). These features suggest the water-fluxed melting of early arc residues occurred in the late stage of growth of continental crust. The crust has been thickened and nearly mature at this stage. This study has great implication on understanding of growth of continental crust in orogenic belts.

Voluminous Jurassic granitoids within the Sanandaj–Sirjan Zone (SSZ) provide insight into the magmatic arc formed in the active margin of Eurasia. Here, we present new in situ zircon U–Pb, whole-rock major and trace element, and Sr–Nd isotopic data for the Gorveh Plutonic Complex (GPC) of the northwestern SSZ in Iran. Six samples from the plutons within the GPC yielded zircon U–Pb ages that range from 151 to 146 Ma. These plutons can be subdivided into two groups based on their geochemistry. Group 1 rocks (the Mobarak Abad diorites and the Gorveh gabbros and diorites) contain relatively high concentrations of the high field strength elements (HFSE; Nb, Ta, Zr, and Ti) and have low Th/Nb (0.20–0.56) and moderate Sm/Yb ratios (1.51–2.32), low (87Sr/86Sr)i values (0.70354–0.70622), and high eNd(t) values (2.3–5.4). These features indicate that the Group 1 rocks formed from magmas derived from a subduction-modified region of the subcontinental lithospheric mantle. The Group 2 plutons (the Bolban Abad granites and the Gorveh quartz monzonites) have A-type granites affinities, including high K2O + Na2O and Zr + Nb + Ce + Y concentrations, and high FeOtot/MgO and 10,000 × Ga/Al ratios. These A-type rocks are enriched in Rb, Th, and K, and depleted in Ba, U, Nb, Ta, Sr, P, and Ti. The Group 2 plutons have different Sr–Nd isotopic compositions to each other, indicating they were derived from different sources and record different igneous processes. The Gorveh quartz monzonites have high (87Sr/86Sr)i ratios (0.70552–0.70617), negative eNd(t) values (−1.1 to −5.4), and extremely low concentrations of MgO (0.32–0.35 wt%), suggesting they were derived from an igneous quartzo-feldspathic crustal source. In comparison, the Bolban Abad granites have positive eNd(t) values and contain high concentrations of SiO2 and low concentrations of MgO, suggesting that they formed from Group 1 magmas that subsequently underwent assimilation and fractional crystallization processes. Combining these new data with the results of previous research, we conclude that this Jurassic magmatism was the result of the formation of a slab window within the subducting Neo-Tethys slab, a process that caused the partial melting of overlying continental lithospheric material.

The concentrations and isotopic geochemistry of Li are potentially useful geochemical tracers of geological processes. To fully utilize Li isotopes as geochemical tracers, it is necessary to characterize the Li isotopic compositions of the various geological reservoirs. However, the Li isotopic composition of the juvenile lower crust is currently poorly constrained. Given that lithospheric architecture of the Tibetan Plateau includes Indian upper/lower crust, Tibetan upper/lower crust and juvenile lower crust, it is necessary to determine the Li isotopic composition for each geological endmember underneath southern Tibet. Among them, the juvenile lower crust was formed directly by underplating of mantle-derived basaltic magma, which is likely to be the critical factor to control the Cu-Au mineralization in southern Tibet and is responsible for crustal thickening beneath southern Tibet. Here, we report the Li concentration and isotopic composition of the juvenile lower crust in southern Tibet. Based on whole-rock major element, trace element, and Sr–Nd–Pb isotopic data, we infer that the Yeba basalts and Gangdese gabbros were derived from partial melting of metasomatized lithospheric mantle, and have compositions similar to the juvenile lower crust. In contrast, the Dianzhong andesites and Gangdese diorites originated from partial melting of the juvenile lower crust. Therefore, these units may be considered representative of the juvenile lower crust. The juvenile lower crust has Li concentrations of 7.1–37.2 ppm (mean = 15.4 ppm), consistent with the Li concentration for the lower crust (13 ppm). Li isotopic compositions (δ7Li) vary from +0.8‰ to +6.6‰ (mean = 3.0‰), similar to values for the EMI/EMII mantle. The Li isotopic compositions of the analyzed samples were not significantly affected by alteration, metamorphism, crustal assimilation, or magmatic differentiation, and therefore represent the isotopic compositions of the juvenile lower crust. The Li systematics of the juvenile lower crust may be attributed to partial melting of subcontinental lithospheric mantle that has undergone metasomatism by Li-rich fluids derived from subducted oceanic crust and marine sediments. Our study also demonstrates near-identical Li isotopic compositions for juvenile lower crust and metasomatized lithospheric mantle, resulting from the lack of Li isotope fractionation during basalt generation and differentiation.

Rare-earth deposits associated with intrusive carbonatite complexes are the world’s most important source of these elements (REE). One of the largest deposits of this type is Maoniuping in the Mianning-Dechang metallogenic belt of eastern Tibet (Sichuan, China). In the currently mined central part of the deposit (Dagudao section), REE mineralization is hosted by a structurally and mineralogically complex Late Oligocene (26.4 ± 1.2 Ma, 40Ar/39Ar age of fluorphlogopite associated with bastnasite) hydrothermal vein system developed in a coeval syenite intrusion. Low-grade stockworks of multiple veinlets and breccias in the lower part of the orebody grade upwards into progressively thicker veins (up to 12 m in width) that are typically zoned and comprise ferromagnesian micas (biotite to fluorphlogopite), sodium clinopyroxenes (aegirine to aegirine-augite), sodium amphiboles (magnesio-arfvedsonite to fluororichterite), K-feldspar, fluorite, barite, calcite, and bastnasite. The latter four minerals are most common in the uppermost 80 m of the Dagudao section and represent the climax of hydrothermal activity. Systematic variations in the fluid inclusion data indicate a continuous hydrothermal evolution from about 230–400 °C (fluid inclusions in feldspar, clinopyroxene, and amphibole) to 140–240 °C (fluid inclusions in bastnasite, fluorite, calcite). Hydrothermal REE transport was probably controlled by F−, (SO4)2−, Cl−, and (CO3)2− as complexing ligands. We propose that at Dagudao, silicate magmas produced orthomagmatic fluids that explored and expanded a fissure system generated by strike-slip faulting. Initially, the fluids had appreciable capacity to transport REE and, consequently, no major mineralization developed. The earliest minerals to precipitate were alkali- and Fe-rich silicates containing low levels of F, which caused progressive enrichment of the fluid in Ca, Mg, F, Cl, REE, (SO4)2−, and (CO3)2−, leading to the crystallization of aegirine-augite, fluororichterite, fluorphlogopite, fluorite, barite, calcite, and bastnasite gradually. Barite, fluorite, calcite, and bastnasite are the most common minerals in typical ores, and bastnasite generally postdates these gangue minerals. Thus, it is very probable that fluid cooling and formation of large amount of fluorite, barite, and calcite triggered bastnasite precipitation in the waning stage of hydrothermal activity.

The giant Zhuxi tungsten deposit is located in the Taqian-Fuchun Ore Belt in northeastern Jiangxi province, and genetically associated with the Zhuxi granitic stocks and dykes. Three mineralization-related granites including granite porphyry dykes (GP), biotite granitic stocks (BG), and white granitic dykes (WG), were identified in the Zhuxi deposit. SHRIMP zircon U–Pb analysis for the three granitic rocks present ages ranging from 153.5 ± 1.0 Ma to 150.4 ± 1.0 Ma. The BG mainly contains quartz, microcline, albite, biotite and muscovite with minor accessory minerals including zircon, apatite, monazite, Ti/Fe oxides, and dolerite. However, the WG is mainly composed of quartz, microcline and albite with minor muscovite and accessory minerals. The GP is a medium-grained porphyritic granite and its phenocrysts include quartz, alkali feldspar, muscovite and plagioclase. All the Zhuxi granites have high SiO2 content (71.97 wt%–81.19 wt%) and total alkali (3.25 wt%–9.42 wt%), and their valid aluminum saturation index (ASI) values show a wide range of 1.03 to 2.49. High Rb/Sr ratios, low Sr content (

Rare earth elements (REEs) are a focus of current research due to their importance in a wide range of industries and technologies. Bayan Obo in China is the largest REE deposit in the world. Although some studies have investigated the banded REE ores in the Bayan Obo deposit, the origin and formation processes of the ores are unclear. In this study, we used X-ray powder diffraction, electron microprobe, laser ablation–inductively coupled plasma–mass spectrometry, and mass spectrometry methods to investigate the mineral assemblages and geochemical characteristics of minerals in banded ores in the Bayan Obo REE deposit. Based on petrographic observations, the early minerals that precipitated were alkali- and Fe-rich silicates, such as aegirine–augite and arfvedsonite, followed by bastnasite, fluorite, barite, calcite, and monazite in the late stage. The REE minerals in the banded REE ores are mainly monazite, bastnasite, and parisite (1–10 vol%) that overprinted gangue minerals, suggesting that REE mineralization occurred during the late hydrothermal stage. The sequence of mineral formation and their evolution caused progressive enrichment in REEs, F, Sr, and Ba. For example, fluorite in the banded REE ores has high concentrations of Sr (252–1910 ppm), Ba (1040–8230 ppm), and light REEs (1001–16,079 ppm), but is depleted in Nb and Ta. The bastnasite is enriched in Sr (885–4046 ppm), Ba (1073–80,809 ppm), and ΣREEs (99,631–158,227 ppm). The fluorite, arfvedsonite, and bastnasite in the banded REE ores have ɛNd(t) values of −3.68–1.78, −5.54, and 0.05, and initial (87Sr/86Sr)i (ISr) ratios of 0.70352–0.70478, 0.70620, and 0.70346, respectively. Based on these data, and the regional geological setting and Pb isotope data, it is proposed that fluorite and bastnasite crystallized from ferrocarbonatite and fine-grained dolomite, and the REE source was a mixture of HIMU mantle and global marine sediments. We also suggest that the carbonatite- or dolomite-hosting ores in Bayan Obo formed by melting of the subcontinental lithospheric mantle, which might have been previously metasomatized by REE- and CO2-rich fluids derived from subducted marine sediments.

The newly discovered Triassic Erdaokan Ag-Pb-Zn deposit having an ore reserve of 2964 kt, with an average grade of 517 g/t Ag, 0.6 wt% Pb and 0.4 wt% Zn, is the only known bitumen-bearing magmatic-hydrothermal Ag-Pb-Zn deposit in the northeastern segment of the Great Xing’an Range, NE China. Its genetic relationship with organic matter remains elusive. In this contribution, we present results from detailed geochemistry, isotope and biomarker studies on bitumen and discuss the genesis of bitumen and its relationship with Ag-Pb-Zn mineralization. The carbon isotope and biomarker analyses suggest a biogenic origin for the organic matter that formed bitumen. We infer that the organic matter was most likely sourced from the carbonaceous shale and limestone belonging to Niqiuhe Formation. Significant interaction between the organic matter and ore-forming fluid is indicated. The light n-alkanes and analogs, alkali elements, vanadium and nickel in the bitumen were removed by the ore-forming fluid, and a variety of metal elements entered into the bitumen. The thermochemical oxidation of methane induced by high-valence metal oxides and thermochemical sulfate reductions were the two main interaction mechanisms between the organic matter and ore-forming fluid, which made an effective contribution to metal precipitation in the Erdaokan Ag-Pb-Zn deposit. On this basis, we propose a genetic model for the genesis of the Erdaokan Ag-Pb-Zn deposit and other hydrocarbon-bearing magmatic-hydrothermal deposits which envisages a significant role played by the organic matter sourced from the sedimentary rocks in ore concentration.

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 bastnasite is unclear, although both pyrite and bastnasite 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.

Late Mesozoic magmatism is extensively developed in the eastern Jiangnan Orogen and is closely related to W, Mo, Cu, Au, and Sn mineralization. Late Mesozoic granitoids show various petrological and mineralizing features that vary spatially (northern Jiangxi Province and southern Anhui Province) and temporally (early stage: 154 to 136 Ma, late stage: 136 to 126 Ma). In this study, we analyzed zircon trace element data from four Late Mesozoic granitoids. Together with published zircon trace element data and biotite compositions from granitoids in the eastern Jiangnan Orogen and W–Sn, Mo and Cu deposits, we use these data to determine the magmatic redox state of the Late Mesozoic granitoids, which is useful in determining mineralization competency and is instructive during exploration. The results show that early stage granitoids of southern Anhui Province are oxidized, characterized by high zircon Ce4+/Ce3+ (median = 278), Ce/Nd (median = 17.1), and EuN/EuN* (median = 0.42) ratios, and high biotite Fe3+/Fe2+ ratios (median = 0.23) and XMg values (median = 0.48). The late stage granitoids of southern Anhui Province are relatively reduced, showing lower zircon Ce4+/Ce3+ (median = 49.7), Ce/Nd (median = 12.7), and EuN/EuN* (median = 0.16) ratios, and lower biotite Fe3+/Fe2+ ratios (median = 0.11) and XMg values (median = 0.38). The early stage granitoids of northern Jiangxi Province show a somewhat reduced redox state. They have comparatively low zircon Ce4+/Ce3+ (median = 17.28), Ce/Nd (median = 4.50), and EuN/EuN* (median = 0.17) ratios, and comparatively low biotite Fe3+/Fe2+ ratios (median = 0.07, N = 160) and XMg values (median = 0.35). The late stage granitoids of northern Jiangxi Province are strongly reduced, characterized by low zircon Ce4+/Ce3+ (median = 17.03), Ce/Nd (median = 0.72), and EuN/EuN* (median = 0.02) ratios, and low biotite Fe3+/Fe2+ ratios (median = 0.06) and XMg values (median = 0.25). Geochemical and isotopic data reveal that early stage granitoids in northern Jiangxi Province were sourced from Neoproterozoic metasedimentary rocks, whereas those in southern Anhui Province originated from Neoproterozoic volcanic–sedimentary sequences. The late stage granitoids in the eastern Jiangnan Orogen formed under an extensional regime and were generated by anatexis with various mantle inputs. The results suggest that early stage granitoids of southern Anhui Province have the potential for Cu (>1 Mt) and Mo (>0.3 Mt) mineralization, whereas late stage granitoids are related to W, Cu (

The giant Dahutang W–Cu–Mo ore field is one of the largest tungsten ore fields worldwide. Three main types of mineralization are developed at Dahutang, comprising veinlet-disseminated, hydrothermal breccia, and coarse quartz vein-type mineralization. In this study, precise muscovite 40Ar/39Ar ages and systematic in situ sulfur isotope compositions of sulfides from the Shimensi and Shiweidong deposits were presented to determine the ore-forming ages and mineralizing intrusions of the hydrothermal breccia type and coarse quartz vein-type mineralization, sources of sulfur in the mineralization, and tectonic setting of the Dahutang ore field. The precise muscovite 40Ar/39Ar dating suggested that the hydrothermal breccia in the Shimensi deposit formed at 142.0 ± 0.6 Ma and was triggered by the biotite granite porphyry (BGP), while the coarse quartz vein-type mineralization in the Shiweidong deposit formed at 136.1 ± 0.5 Ma and was caused by an early episode of coarse-grained porphyritic two-mica granite (CPTG; 144.2–137.5 Ma) and destroyed by the late episode of CPTG (130–128 Ma). The in situ sulfur isotope compositions of sulfides showed that the hydrothermal breccia type and the coarse quartz vein-type mineralization had a narrow range of sulfur isotope compositions (−3.38–+0.39‰), implying a magmatic origin for sulfur. The increased sulfur isotopes in the sulfides from early to late stages were probably caused by a reduction in the oxygen fugacity of ore-forming fluids in the hydrothermal breccia mineral system. The main W–Cu–Mo mineralization event at Dahutang occurred in the 146–136 Ma interval and was only associated with the early episode of magmatism (149–138 Ma), which coincided well with the Cu–Au–Mo–Fe mineral system in the neighboring Middle–Lower Yangtze River Metallogenic Belt (148–135 Ma). The late episode of magmatism (138–128 Ma), however, was commonly emplaced after the tungsten polymetallic mineralization and even destroyed early formed orebodies as ore-barren intrusions. Combined with the regional tectonic evolution, we proposed that the W–Cu–Mo mineralization and ore-related granites in the Dahutang ore field formed in a transitional setting from a compressional regime to an extensional regime.

Dating of bitumen can potentially constrain both the timing of mineralization and hydrocarbon deposition in hydrocarbon-bearing hydrothermal deposits. Here we report for the first time direct Sm-Nd dating on bitumen from the Erdaokan Ag-Pb-Zn deposit, a newly discovered, large, hydrocarbon-bearing hydrothermal deposit with 2964 kt of ore and 1535 t Ag with an average grade of 517 g/t Ag, 0.6 wt% Pb and 0.41 wt% Zn in the Back-Arc basin of NE Great Xing’an Range, NE China. Dating results show that Sm-Nd isochron age of four bitumen samples is 234.6 ± 1.2 Ma and an isochron age that includes three galena and four bitumen samples is 234.9 ± 1.4 Ma. In order to verify these ages, we performed Rb-Sr dating on pyrite and galena from the same deposit and U-Pb dating of zircon from the adjacent diorite porphyrite dike, which yielded ages of 232.9 ± 2.3 Ma and 234.2 ± 2.8 Ma, respectively. The highly concordant ages from multiple techniques confirms that bitumen Sm-Nd isotopic dating is reliable, and that the ages obtained in our study represent the hydrocarbon deposition as well as mineralization timing in the deposit. We conclude that, in the Duobaoshan metallogenic belt, the Erdaokan Ag-Pb-Zn deposit is the first identified large, Middle Triassic, hydrocarbon-bearing silver-lead–zinc deposit and is of great significance to the regional metallogenesis research and prospecting work in the Great Xing’an Range.

Fault zones control the locations of many ore deposits, but the ore-forming processes in such fault zones are poorly understood. We have studied the deformation and ore textures associated with fault zones that controlled the lead–zinc mineralization of the Dongmozhazhua deposit, central Tibet, ∼100 km southwest of Yushu City. Geological mapping shows that the structural framework of the Dongmozhazhua area is defined by NW–SE-trending reverse faults and superposed folds that indicate at least two stages of deformation. The first stage is characterized by tight nearly E–W-striking folds that formed during the closure of the Jinshajiang Paleo-Tethyan Ocean in the Triassic. The second stage of deformation produced NW–SE-trending reverse faults and related structures of the Fenghuoshan–Nangqian fold-and-thrust belt associated with India–Asia collision in the late Eocene to Oligocene. Scanline surveys along the ore-controlling fault zones show an internal structure that comprises a damage zone, a breccia zone with clasts that have become rounded, and a breccia zone with lenticular clasts, and this complex architecture was formed during at least two compressional substages of deformation. The Pb–Zn mineralization in the Dongmozhazhua area occurs exclusively close to NW–SE-trending reverse fault zones. Microtextural observations reveal that mineralization occurred as veinlets and disseminated blebs in limestone clasts, and as continuous bands and cements in fractured rocks. Cataclastic sulfide grains also can be seen in the matrix of some fault zones. The types of mineralization differ with structural position. The fillings of the ore-bearing veinlets typify the products of hydraulic fracture and both types of mineralization took place concurrently with regional contraction. We consider, therefore, that the ore-bearing fluids in the Dongmozhazhua deposit were concentrated in fault zones during regional compression and that the ore minerals were precipitated during hydraulic fracturing of host rocks. Subsequent fault activity pulverized some pre-existing sulfide material into cataclastic grains in the matrix of a tectonic breccia that developed in the same faults.

In addition to well-known subduction processes, the collision of two continents also generates abundant ore deposits, as in the case of the Tibetan Plateau, which is the youngest and most spectacular collisional belt on Earth. During the building history of the Gangdese magmatic belt, several magmatic flare-up events developed, however, significant magmatic-hydrothermal lead–zinc mineralization dominantly accompanied the magmatism during the syncollisional period (~ 65–41 Ma). Based on integrated geochemical and isotopic data, we provide insights into the genesis and evolution of syncollisional magmas, and their implications for significant magmatic-hydrothermal lead–zinc mineralization. The Sr–Nd isotopic compositions of most syncollisional igneous rocks (87Sr/86Sr = 0.7034–0.7123; eNd(t) = − 9.0 to + 1.8) indicate a mixing origin between mantle-derived basaltic magmas and ancient crustal melts, and fractional crystallization is a fundamental mechanism by which syncollisional magmas evolve towards intermediate to silicic compositions. Most lead–zinc mineralization-related plutons are high silica (76.14% wt.% SiO2 on average), high oxygen fugacity (average ΔFMQ + 2.5) granites with highly evolved chemical signatures [average Eun/Eun* = 0.33, high Rb/Sr (average = 3.9)], and they represent the final products from primary magmas. Due to the contribution of ancient crustal melts to the genesis of mineralization-related parent magmas, the spatial distribution of Pb–Zn deposits within the northern Gangdese magmatic belt is controlled by the lithospheric architecture. In compressional environments, magmas have low evacuation efficiency and long magma chamber lifespan, which is favorable for basaltic parents evolved to high silica granites through sufficient fractional crystallization. This scenario contributes to our understanding of the significant magmatic-hydrothermal lead–zinc mineralization that occurred in the syncollisional period.

The Paleo-Tethyan tectonic evolution of north-central Tibet remains controversial, particularly regarding the nature and extension of associated sutures. The Yushu melange, located in the junction part of the western Jinshajiang, the southern Jinshajiang and the Ganzi–Litang sutures, is a key area to reveal the Paleo-Tethyan tectonics of this area. This study presents new geochronological and geochemical data for the Zhimenda volcanic suite of the Yushu Melange. These rocks preserve a record of back-arc magmatism along the northern margin of the North Qiangtang Block. The Zhimenda volcanics are composed of ignimbrite, basalt, and porphyritic tuff intercalated with terrigenous clastic rocks. Zircon 206 Pb/ 238 U ages of the ignimbrites indicate they formed at ~ 254 Ma. The basalts are relatively enriched in large-ion lithophile elements and depleted in high field strength elements. Their high MgO, Ni, and Cr contents, relatively high Sm/Yb and Rb/Nb values, and positive zircon e Hf (t) and bulk e Nd (t) values suggest they were derived from the partial melting of a depleted subcontinental lithospheric mantle source metasomatized by hydrous fluids. The Zhimenda basalts are geochemically similar to back-arc basin basalts in the Okinawa Trough. They were erupted related to subduction of the Longmuco–Shuanghu Paleo-Tethyan oceanic plate beneath the North Qiangtang Block. We propose that the Yushu Melange converges with the Ganzi–Litang Suture Zone to the east, rather than with the Jinshajiang Suture Zone to the southeast, and that a huge Permian trench–arc–back-arc system developed in north-central Tibet.

The lithium isotopic compositions of adakitic rocks and K-rich volcanic rocks in southern Tibet range from + 1.3‰ to + 7.5‰ and − 4.9‰ to + 3.5‰, respectively. The subduction of the Indian Plate beneath the Lhasa Terrane means that traditional lithium isotopic compositions of various reservoirs are unable to explain the aforementioned δ7Li data. Therefore, it is necessary to determine the Li isotopic compositions of the different geological endmembers underneath southern Tibet. Here, we report the lithium isotopic composition and concentration of Indian upper and lower continental crust. On the basis of whole-rock major and trace element data and Sr–Nd–Pb isotope data, leucogranites from Luozha and Longzi are considered as representative of Indian upper crust, whereas two-mica granites from Quedang and Dala and granulites and gneisses from Nyalam are considered as representative of Indian lower crust. The Li concentration of Indian upper crust varies from 23 to 45 ppm with a mean of 34 ppm, consistent with a weighted mean Li concentration for the upper crust of 35 ± 11 ppm. In contrast, the Li abundance of Indian lower crust is estimated to be 33–84 ppm with a mean of 58 ppm, much higher than the average Li concentration for the lower crust of ~ 8 ppm because of the high modal abundance of biotite and muscovite. The Li isotopic compositions (+ 0.9‰ to + 5.6‰) of Indian upper continental crust are relatively heavy compared with the average Li isotopic composition of upper continental crust. On the other hand, the Li isotopic compositions of Indian lower continental crust (− 4.4‰ to − 0.1‰) are lighter than those of Indian upper continental crust. The isotopically heavy signature of Indian upper crust is produced by high-δ7Li fluids released from the Indian lower crust slab, whereas the lighter signature of Indian lower crust is generated by the partial melting of residual Indian lower crust slab during metamorphic dehydration of Indian lower crust.

The Xiadan gold deposit from Jiaodong Peninsula contains more than 200 t of gold, and is one of the representative largest deposits within south part of the Zhaoping Fault zone. The gold orebodies consist of auriferous altered rocks that show disseminated and stockwork mineralization. Mineralization and alteration are structurally controlled by the NE- to NNE-striking Linglong detachment fault. Mineralization can be divided into three stages: (K-feldspar)–sericite–quartz–pyrite, quartz–gold–polymetallic sulfide, and quartz–carbonate, with the majority of the gold being produced during the middle stage. Based on a combination of petrography, microthermometry, and laser Raman spectroscopy, three types of fluid inclusion were identified in the vein mineral assemblages: NaCl–H2O (A-type), CO2–H2O–NaCl (AC-type), and pure CO2 (PC-type). Quartz crystals in veins that formed during the early stage contain mainly AC-type primary fluid inclusions, with rare PC-type inclusions. These fluid inclusions homogenize completely at temperatures of 253°C–408°C and have medium–low salinities (1.62–11.89 wt.% NaCl equivalent). Quartz crystals that formed during the middle stage contain all three types of fluid inclusion, and these fluid inclusions homogenize completely at temperatures of 176°C–335°C and have salinities of 0.70–14.73 wt.% NaCl equivalent. In contrast, quartz that formed during the last stage contains only A-type fluid inclusions; these inclusions have homogenization temperatures of 108°C–253°C and salinities of 1.73–11.60 wt.% NaCl equivalent. The above data indicate that the ore-forming system evolved from a CO2-rich mesothermal fluid into a CO2-poor fluid as a result of an influx of meteoric water. Fluid immiscibility is an essential prerequisite for metals precipitation in Xiadian. The characteristics of fluid inclusions, combined with H–O–S isotopes suggest that the ore-forming fluids might be of metamorphic origin. Based on the immiscibility of AC-type fluid inclusions, trapping pressures have been estimated at 88–339 MPa during ore formation, with a depth of metallogenesis of 8.8–12.6 km. The depth of erosion of study area has been calculated as about 10.3 km between 130 Ma and the present. Considering the gold mineralization occurred at around 130 Ma, the space with deep gold exploration is expectable at Xiadian.

The Sanjiang metallogenic belt includes a variety of economically important carbonate-hosted Pb-Zn deposits that share some similarities with classic Mississippi Valley-type (MVT) ore deposits but are hosted within a thrust belt rather than an orogenic foreland. This study aims to clarify the origin of mineralizing fluids responsible for this style of mineralization. Fluid inclusions trapped in ore-stage carbonate and fluorite from these deposits have salinities of ~6 to 28 wt % NaCl equiv and homogenization temperatures of 70° to 370°C that extend to much higher values than are typical of MVT deposits. The majority of ore-stage samples have fluid inclusion molar Br/Cl ratios of between seawater (1.5 × 10 −3 ) and (2.86 ± 0.04) × 10 −3 , but low-salinity fluid inclusions in late calcite have lower Br/Cl of less than (0.55 ± 0.01) × 10 −3 . In contrast, fluid inclusion molar I/Cl ratios are uniformly greater than the seawater value of ~0.8 × 10 −6 and extend from (2.1 ± 1.1) × 10 −6 to (506 ± 12) × 10 −6 . This range of Br/Cl and I/Cl values is similar to what has been reported for fluid inclusions in other MVT districts and together with the fluid salinity implies the ore-forming fluids had a dominant origin from basinal brines (e.g., sedimentary formation waters) formed by the subaerial evaporation of seawater; all the fluids were influenced by addition of organic Br and I derived from the sedimentary host rocks and some fluids were locally modified by interaction with evaporites producing low Br/Cl ratios. The fluid inclusions have 40 Ar/ 36 Ar ratios of up to 441 that are higher than the atmospheric value of 296 and typical of carbonate sedimentary rocks. The fluid inclusions have high concentrations of atmospheric 36 Ar and variable 129 Xe/ 36 Ar and 84 Kr/ 36 Ar ratios that are outside the range expected from mixing air and air-saturated water. These data are likely to reflect a complex fluid history involving acquisition of atmospheric ( 36 Ar, 84 Kr, 129 Xe) and radiogenic (e.g., 40 Ar ✼ ) noble gases trapped in sedimentary rocks and fractionation of these gases between water and hydrocarbons. The 3 He/ 4 He ratios of fluorite fluid inclusions range from a typical crustal value of 0.061 ± 0.004 to values of >0.7 Ra, indicating a minor component of mantle-derived 3 He. The fluids with the highest 3 He/ 4 He also have 4 He/ 40 Ar ✼ close to the mantle value, suggesting the 3 He could have been introduced by a volumetrically minor fluid of either magmatic or deep metamorphic origin ( 40 Ar ✼ = radiogenic 40 Ar). The new halogen and noble gas data are consistent with a model in which regional Pb-Zn mineralization formed by mixing two modified basinal brines that were transported through independent aquifers and fluid pathways to the sites of mineralization. A low-temperature brine contained organic Br, I, and H 2 S, and a high-temperature metal-rich brine (>370°C) that included a volumetrically minor magmato-metamorphic component was channeled up deeply penetrating thrust structures.

The recently discovered Zhuxi W–Cu ore deposit is located within the Taqian–Fuchun Ore Belt in the southeastern edge of the Yangtze Block, South China. Its inferred tungsten resources, based on new exploration data, are more than 280 Mt by 2016. At least three paragenetic stages of skarn formation and ore deposition have been recognized: prograde skarn stage; retrograde stage; and hydrothermal sulfide stage. Secondly, greisenization, marmorization and hornfels formation are also observed. Scheelite and chalcopyrite are the dominant metal minerals in the Zhuxi deposit and their formation was associated with the emplacement of granite stocks and porphyry dykes intruded into the surrounding Carboniferous carbonate sediments (Huanglong and Chuanshan formations) and the Neoproterozoic slate and phyllites. The scheelite was mostly precipitated during the retrograde stage, whereas the chalcopyrite was widely precipitated during the hydrothermal sulfide stage. A muscovite 40Ar/39Ar plateau age of about 150 Ma is interpreted as the time of tungsten mineralization and molybdenite Re–Os model ages ranging from 145.9 ± 2.0 Ma to 148.7 ± 2.2 Ma (for the subsequent hydrothermal sulfide stage of activity) as the time of the copper mineralization. Our new molybdenite Re–Os and muscovite 40Ar/39Ar dating results, along with previous zircon U–Pb age data, indicate that the hydrothermal activity from the retrograde stage to the last hydrothermal sulfide stage lasted up to 5 Myr, from 150.6 ± 1.5 to 145.9 ± 1 Ma, and is approximately coeval or slightly later than the emplacement of the associated granite porphyry and biotite granite. The new ages reported here confirm that the Zhuxi tungsten deposit represents one of the Mesozoic magmatic–hydrothermal mineralization events that took place in South China in a setting of lithospheric extension during the Late Jurassic (160–150 Ma). It is suggested that mantle material played a role in producing the Zhuxi W–Cu mineralization and associated magmatism.

Understanding the geological history of the Lhasa Terrane prior to the India–Asia collision (~ 55 ± 10 Ma) is essential for improved models of syn-collisional and post-collisional processes in the southern Lhasa Terrane. The Miocene (~ 18–10 Ma) adakitic magmatism with economically significant porphyry-type mineralization has been interpreted as resulting from partial melting of the Jurassic juvenile crust, but how this juvenile crust was accreted remains poorly known. For this reason, we carried out a detailed study on the volcanic rocks of the Yeba Formation (YF) with the results offering insights into the ways in which the juvenile crust may be accreted in the southern Lhasa Terrane in the Jurassic. The YF volcanic rocks are compositionally bimodal, comprising basalt/basaltic andesite and dacite/rhyolite dated at 183–174 Ma. All these rocks have an arc-like signature with enriched large ion lithophile elements (LILEs; e.g., Rb, Ba and U) and light rare earth elements (LREEs) and depleted high field strength elements (HFSEs; e.g., Nb, Ta, Ti). They also have depleted whole-rock Sr–Nd and zircon Hf isotopic compositions, pointing to significant mantle isotopic contributions. Modeling results of trace elements and isotopes are most consistent with the basalts being derived from a mantle source metasomatized by varying enrichment of subduction components. The silicic volcanic rocks show the characteristics of transitional I–S type granites, and are best interpreted as resulting from re-melting of a mixed source of juvenile amphibole-rich lower crust with reworked crustal materials resembling metagraywackes. Importantly, our results indicate northward Neo-Tethyan seafloor subduction beneath the Lhasa Terrane with the YF volcanism being caused by the initiation of back-arc rifting. The back-arc setting is a likely site for juvenile crustal accretion in the southern Lhasa Terrane.

The deep crustal continental components and architecture of the western Central Asian Orogenic Belt (CAOB) have long been a matter of debate. This article presents an integrated study of published geochronological and Hf-in-zircon isotopic data for inherited zircons from the Palaeozoic granitoid rocks and associated felsic volcanic rocks of the Chinese Altai, East Junggar, and nearby regions. The aim is to trace the age spatial distribution of deep old crustal components. Our data set comprises 463 published age data obtained by SHRIMP and LA-ICP-MS from felsic igneous rocks in these areas. Among these samples, zircon xenocrysts were observed in 69 granitic rocks and 15 felsic volcanic rocks from the Chinese Altai and 30 granitoid rocks and five felsic volcanic rocks in the East Junggar, respectively.Three major zircon xenocrysts provinces are defined based on the distribution of these inherited zircon ages, combined with Hf-in-zircon isotopes. Province I, mainly situated in the eastern part of th...