Chronology,geochemistry and Sr–Nd isotope studies of Jurassic intrusions in the Diyanqinamu porphyry Mo mine,central Inner Mongolia,China

Available cores of porphyritic granite and aplitic granite from the Diyanqinamu porphyry Mo deposit in the north central Great Xing’an Range presented an opportunity to examine and analyze Mesozoic igneous rocks far from the Paleo-Pacific subduction zone. The Diyanqinamu granites are highly fractionated I-type, distinguished from the M-, A- or S-type granite by: high SiO₂, and Rb; low Zr, Nb, Y, and Ce; low Fe₂O₃^total/MgO and (K₂O + Na₂O)/CaO ratios; low alumina saturation index (<1.1); low initial I_Sr ratios (0.70137–0.70451); positive εNd(t) values (2.37–3.77); and negative correlation between P₂O₅ and SiO₂. The aplitic granites were generated by fractional crystallization of the porphyritic granite, as evidenced by: spatial proximity; consistent zircon U–Pb ages (156 Ma) within error; correlations between other oxides and SiO₂ in Haker diagrams; low Ba, Sr, Nb, P, Ti, Eu; linear relationship in both (La/Yb)_N vs. La and Sr vs. Ba diagrams; and, decreasing LREE and ∑REE with increasing SiO₂. The Diyanqinamu granites have young depleted-mantle two-stage model ages (avg. T_DM2 = 660 Ma) similar to those of most Mesozoic voluminous felsic magmas in northeastern China, and were likely sourced from pre-existent crustal components both “old” and juvenile that had been juxtaposed during the tectonic evolution of the Paleo-Asian Ocean. These granites project in the transitional field from syn-collision to post-collision tectonic settings on tectonic discrimination diagrams, implying emplacement in an extensional environment. Extensional volcanism and basin formation in the Great Xing’an Range region in Late Jurassic is coeval with the Diyanqinamu granites, demonstrating that post-orogenic lithospheric extension related to the closure of the Mongol-Okhotsk Ocean was the main driving force for Late Jurassic magmatism in this region.     

Geology,geochemistry, and geochronology of the Wangjiazhuang porphyry–breccia Cu(–Mo) deposit in the Zouping volcanic basin,eastern North China Block

The Wangjiazhuang porphyry–breccia Cu(–Mo) deposit is located in the Zouping volcanic basin, western Shandong Province. Seven molybdenite samples yield a Re–Os weighted mean age of 127.8 ± 0.7 Ma (2σ), which is identical within error to the zircon weighted mean ²⁰⁶Pb/²³⁸U age of 128.3 ± 1.3 Ma (2σ) determined for quartz monzonite samples. The host rock is characterized by high concentrations of K₂O (4.26–4.53 wt.%), Na₂O (4.97–5.76 wt.%), LILEs and LREEs, and high Mg# (> 40), and low concentrations of HFSEs and HREEs, with K₂O/Na₂O ratios of 0.76–0.88. The quartz monzonite also has high Sr/Y (69.9–112.5) and (La/Yb)_N (22.0–30.0) ratios, similar to adakitic rocks worldwide. Relatively low initial ⁸⁷Sr/⁸⁶Sr ratios (0.70549–0.70556), high ε_Nd(t) values (2.58–3.06), high radiogenic Pb [(²⁰⁶Pb/²⁰⁴Pb)i = 18.3424–18.4606, (²⁰⁷Pb/²⁰⁴Pb)_i = 15.5692–15.5985, (²⁰⁸Pb/²⁰⁴Pb)_i = 38.1714–38.2734] and high zircon ε_Hf(t) values (− 2.1 to + 4.3) indicate that the magma was likely derived from the partial melting of subducted oceanic crust which then reacted with the peridotitic mantle wedge. Both the breccia and porphyry ores have a narrow range of δ³⁴S (− 4.8 to + 2.1‰) and Pb isotopic compositions (²⁰⁶Pb/²⁰⁴Pb = 18.295–18.402, ²⁰⁷Pb/²⁰⁴Pb = 15.551–15.573, and ²⁰⁸Pb/²⁰⁴Pb = 38.215–38.331), suggesting that the ore metals were extracted primarily from the quartz monzonite or similar source. Subduction of the Paleo-Pacific slab during the Early Cretaceous resulted in the formation of the Wangjiazhuang quartz monzonite and associated Cu(–Mo) deposit in western Shandong Province.     

Geochronology,geochemistry and Sr–Nd–Hf isotopes of the Haisugou porphyry Mo deposit,northeast China,and their geological significance

The Haisugou Mo deposit is located in the northern part of the Xilamulun Mo–Cu metallogenic belt in northeastern China. The Mo mineralization mainly occurs as quartz-molybdenite veins within the Haisugou granite, which was emplaced into rocks of the Early Permian Qingfengshan Formation. Zircon U–Pb dating by LA–ICP-MS of the granite yields a crystallization age of 137.6 ± 0.9 Ma, suggesting emplacement during the peak time of Mo mineralization in eastern China, broadly constrained to ca. 150–130 Ma, when tectonic stresses shifted from compression to extension. Whole-rock geochemical data suggest that the granite belongs to the high-K calc-alkaline series, and is characterized by relatively high LREE; low HREE; depletion of Ti, Ba, and Nb; and a moderate negative Eu anomaly. The zircon ε_Hf(t) and whole-rock ε_Nd(t) values for the intrusion range from +4.5 to +10.0 and +0.2 to +1.6, respectively, indicating that the magma originated from the juvenile lower crust source derived from depleted mantle, with some component of ancient continental crust. The granite is also characterized by initial (⁸⁷Sr/⁸⁶Sr)_i ratios ranging from 0.7040 to 0.7074, which suggest some contamination by the upper crust during the ascent of the primitive magma. Moreover, it can be recognized from the whole-rock major and trace element data that significant fractional crystallization occurred during magmatic evolution, with the separation of plagioclase and K-feldspar. Because Mo is an incompatible element and tends to concentrate in the melt during crystallization, fractionation processes likely played an important role in the formation of the Haisugou Mo deposit.     

Magmatic evolution of the Tuwu–Yandong porphyry Cu belt,NW China: Constraints from geochronology,geochemistry and Sr–Nd–Hf isotopes

The Tuwu–Yandong porphyry Cu belt is located in the Eastern Tianshan mountains in the eastern Central Asian Orogenic Belt. Petrochemical and geochronological data for intrusive and volcanic rocks from the Tuwu and Yandong deposits are combined with previous studies to provide constraints on their petrogenesis and tectonic affinity. New LA–ICP–MS zircon U–Pb ages of 348.3 ± 6.0 Ma, 339.3 ± 2.2 Ma, 323.6 ± 2.5 Ma and 324.1 ± 2.3 Ma have been attained from intrusive units associated with the deposits, including diorite, plagiogranite porphyry, quartz albite porphyry and quartz porphyry, respectively. The basalt and andesite, which host part of the Cu mineralization, are tholeiitic with high Al₂O₃, Cr, Ni and low TiO₂ contents, enriched LREEs and negative HFSE (Nb, Ta, Zr, Ti) anomalies consistent with arc magmas. Diorites are characterized by low SiO₂ content but high MgO, Cr and Ni contents, similar to those of high-Mg andesites. The parental magma of the basalt, andesite and diorite is interpreted to have been derived from partial melting of mantle-wedge peridotite that was previously metasomatized by slab melts. The ore-bearing plagiogranite porphyry is characterized by high Na₂O, Sr, Cr and Ni contents, low Y and Yb contents, low Na₂O/K₂O ratios and high Sr/Y ratios and high Mg#, suggesting an adakitic affinity. The high ε_Nd(t) (5.02–9.16), low I_Sr (0.703219–0.704281) and high ε_Hf(t) (8.55–12.99) of the plagiogranite porphyry suggest they were derived by a partial melting of the subducted oceanic crust followed by adakitic melt-mantle peridotite interaction. The quartz albite porphyry and quartz porphyry are characterized by similar Sr–Nd–Hf isotope but lower Mg# and whole-rock (La/Yb)_N ratios to the plagiogranite porphyry, suggesting they were derived from juvenile lower crust, and negative Eu anomalies suggest fractionation of plagioclase. We propose that a flat subduction that started ca. 340 Ma and resulted in formation of the adakitic plagiogranite porphyry after a period of “steady” subduction, and experienced slab rollback at around 323 Ma.     

Hydrothermal evolution of the Sar-Cheshmeh porphyry Cu–Mo deposit,Iran: Evidence from fluid inclusions

The Sar-Cheshmeh porphyry Cu–Mo deposit is located in Southwestern Iran (∼65 km southwest of Kerman City) and is associated with a composite Miocene stock, ranging in composition from diorite through granodiorite to quartz-monzonite. Field observations and petrographic studies demonstrate that the emplacement of the Sar-Cheshmeh stock took place in several pulses, each with associated hydrothermal activity. Molybdenum was concentrated at a very early stage in the evolution of the hydrothermal system and copper was concentrated later. Four main vein Groups have been identified: (I) quartz+molybdenite+anhydrite±K-feldspar with minor pyrite, chalcopyrite and bornite; (II) quartz+chalcopyrite+pyrite±molybdenite±calcite; (III) quartz+pyrite+calcite±chalcopyrite±anhydrite (gypsum)±molybdenite; (IV) quartz±calcite±gypsum±pyrite±dolomite. Early hydrothermal alteration produced a potassic assemblage (orthoclase-biotite) in the central part of the stock, propylitic alteration occurred in the peripheral parts of the stock, contemporaneously with potassic alteration, and phyllic alteration occurred later, overprinting earlier alteration. The early hydrothermal fluids are represented by high temperature (350–520 °C), high salinity (up to 61 wt% NaCl equivalent) liquid-rich fluid inclusions, and high temperature (340–570 °C), low-salinity, vapor-rich inclusions. These fluids are interpreted to represent an orthomagmatic fluid, which cooled episodically; the brines are interpreted to have caused potassic alteration and deposition of Group I and II quartz veins containing molybdenite and chalcopyrite. Propylitic alteration is attributed to a liquid-rich, lower temperature (220–310 °C), Ca-rich, evolved meteoric fluid. Influx of meteoric water into the central part of the system and mixing with magmatic fluid produced albitization at depth and shallow phyllic alteration. This influx also caused the dissolution of early-formed copper sulphides and the remobilization of Cu into the sericitic zone, the main zone of the copper deposition in Sar-Cheshmeh, where it was redeposited in response to a decrease in temperature.     

Origin of the Tongshankou porphyry–skarn Cu–Mo deposit,eastern Yangtze craton,Eastern China: geochronological,geochemical, and Sr–Nd–Hf isotopic constraints

The Tongshankou Cu–Mo deposit, located in the westernmost Daye district of the Late Mesozoic Metallogenic Belt along the Middle-Lower reaches of the Yangtze River, eastern China, consists mainly of porphyry and skarn ores hosted in the Tongshankou granodiorite and along the contact with the Lower Triassic marine carbonates, respectively. Sensitive high-resolution ion microprobe zircon U–Pb dating constrains the crystallization of the granodiorite at 140.6 ± 2.4 Ma (1σ). Six molybdenite samples from the porphyry ores yield Re–Os isochron age of 143.8 ± 2.6 Ma (2σ), while a phlogopite sample from the skarn ores yields an ⁴⁰Ar/³⁹Ar plateau age of 143.0 ± 0.3 Ma and an isochron age of 143.8 ± 0.8 Ma (2σ), indicating an earliest Cretaceous mineralization event. The Tongshankou granodiorite has geochemical features resembling slab-derived adakites, such as high Sr (740–1,300 ppm) and enrichment in light rare earth elements (REE), low Sc (<10 ppm), Y (<13.3 ppm), and depletion in heavy REE (<1.2 ppm Yb), and resultant high Sr/Y (60–92) and La/Yb (26–75) ratios. However, they differ from typical subduction-related adakites by high K, low MgO and Mg#, and radiogenic Sr–Nd–Hf isotopic compositions, with (⁸⁷Sr/⁸⁶Sr) _t  = 0.7062–0.7067, ɛ _Nd(t) = −4.37 to −4.63, (¹⁷⁶Hf/¹⁷⁷Hf) _t  = 0.282469–0.282590, and ɛ _Hf(t) = −3.3 to −7.6. The geochemical and isotopic data, coupled with geological analysis, indicate that the Tongshankou granodiorite was most likely generated by partial melting of enriched lithospheric mantle that was previously metasomitized by slab melts related to an ancient subduction system. Magmas derived from such a source could have acquired a high oxidation state, as indicated by the assemblage of quartz–magnetite–titanite–amphibole–Mg-rich biotite in the Tongshankou granodiorite and the compositions of magmatic biotite that fall in the field between the NiNiO and magnetite–hematite buffers in the Fe³⁺–Fe²⁺–Mg diagram. Sulfur would have been present as sulfates in such highly oxidized magmas, so that chalcophile elements Cu and Mo were retained as incompatible elements in the melt, contributing to subsequent mineralization. A compilation of existing data reveals that porphyry and porphyry-related Cu–Fe–Au–Mo mineralization from Daye and other districts of the Metallogenic Belt along the Middle-Lower reaches of the Yangtze River took place coevally in the Early Cretaceous and was related to an intracontinental extensional environment, distinctly different from the arc-compressive setting of the Cenozoic age that has been responsible for the emplacement of most porphyry Cu deposits of the Pacific Rim.     

Geodynamic setting of the Zijinshan porphyry–epithermal Cu–Au–Mo–Ag ore system,SW Fujian Province,China: Constrains from the geochronology and geochemistry of the igneous rocks

Zijinshan is a large porphyry–epithermal Cu–Au–Mo–Ag ore system located in the Zijinshan mineral field (ZMF) of southwestern Fujian Province, China. Although it is commonly accepted that the early Cretaceous magmatism and the metallogenesis of the mineral field are closely related, the tectonic setting for the ore-forming event(s) has been controversial and regarded as either extensional or subduction-related. New U–Pb zircon geochronology, Sr–Nd–Pb isotopic systematics, and geochemical data presented here from granites and volcanic rocks in the mineral field help to clarify this uncertainty.LA–MC–ICP-MS U–Pb zircon analyses yield weighted mean ages of between ca. 165 and 157 for the monzogranite, ca. 112 Ma for granodiorite, and between ca. 111 and 102 Ma for nine samples of volcanic units in the study area. These dates, integrated with previous geochronological data, indicate that there were two magmatic events in the area during the Middle to Late Jurassic and the Early Cretaceous. Major and trace element geochemistry indicates that these rocks are high-K, calc-alkaline granites, are enriched in LREE and Th, U, Ta, Nd, Sm and Yb, and depleted in Ba, K, Sr, P, Ti and Y. These features are characteristic of volcanic-arc granites or active-continental margin granites. The Middle to Late Jurassic monzogranitic plutons in the region have initial ⁸⁷Sr/⁸⁶Sr ratios of 0.7096 to 0.7173, εNd_T values of − 10.1 to − 7.6, ²⁰⁶Pb/²⁰⁴Pb isotope ratios of 18.51–18.86, ²⁰⁷Pb/²⁰⁴Pb isotope ratios of 15.64–15.73, and ²⁰⁸Pb/²⁰⁴Pb isotope ratios of 38.76–39.18. The Early Cretaceous granodiorite and volcanic rocks are distinctly different with initial ⁸⁷Sr/⁸⁶Sr ratios of 0.7055–0.7116, εNd_T values of − 8 to 0.5, ²⁰⁶Pb/²⁰⁴Pb ratios ranging between 18.49 and 19.77, ²⁰⁷Pb/²⁰⁴Pb ratios of 15.63–15.71, and ²⁰⁸Pb/²⁰⁴Pb ratios of 38.71–40.62. These characteristics suggest that the source for the Middle to Late Jurassic monzogranitic plutons is a partially melted Mesoproterozoic substrate, with a minor component from Paleozoic material, whereas the Early Cretaceous granodiorite and volcanic rocks may represent mixing of crustal and mantle-derived melts. It is therefore suggested that the Middle to Late Jurassic monzogranitic plutons, and the Early Cretaceous granodiorite and volcanic rocks in the ZMF are the result of an active continental-margin setting related to the subduction of the Paleo-Pacific Plate beneath the Eurasian continent. Given that the mineralization and the early Cretaceous granodiorite and volcanic rocks in the area are genetically related, the Zijinshan porphyry–epithermal ore system formed in the subduction-related tectonic setting.     

Geochemical and Sr–Pb–Nd isotopic characteristics of the Shakhtama porphyry Mo–Cu system (Eastern Transbaikalia,Russia)

The Shakhtama Mo–Cu porphyry deposit is located within the eastern segment of the Central Asian Orogenic Belt, bordering the southern margin of the Mongol–Okhotsk suture zone. The deposit includes rocks of two magmatic complexes: the precursor plutonic (J₂) and ore-bearing porphyry (J₃) complexes. The plutonic complex was emplaced at the final stages of the collisional regime in the region; the formation of the porphyry complex may have overlapped with a transition to extension. The Shakhtama rocks are predominantly metaluminous, I-type high K calc-alkaline to shoshonitic in composition, with relatively high Mg#, Ni, Cr and V. They are characterized by crustal-like I_Sr (0.70741–0.70782), relatively radiogenic Pb isotopic compositions, ε_Nd(T) values close to CHUR (−2.7 to +2.1) and Nd model ages from 0.8 to 1.2 Ga. Both complexes are composed of rocks with K-adakitic features and rocks without adakite trace element signatures. The regional geological setting together with geochemical and isotopic data indicate that both juvenile and old continental crust contributed to their origin. High-Mg# K-adakitic Shakhtama magmas were most likely generated by partial melting of thickened lower crust during delamination and interaction with mantle material, while magmas lacking adakite-like signatures were probably generated at shallower levels of lower crust. The derivation of melts, related to the formation of plutonic and porphyry complexes involved variable amounts of old Precambrian lower crust and juvenile Phanerozoic crust. Isotopic data imply stronger contribution of juvenile mantle-derived material to the fertile magmas of the porphyry complex. Juvenile crust is proposed as an important source of fluids and metals for the Shakhtama ore-magmatic system.     

U–Pb dating,geochemistry, and Sr–Nd isotopic composition of a granodiorite porphyry from the Jiadanggen Cu–(Mo) deposit in the Eastern Kunlun metallogenic belt,Qinghai Province,China

The Jiadanggen porphyry Cu–(Mo) deposit is newly discovered and located in the Eastern Kunlun metallogenic belt of Qinghai Province, China. Here, we present a detailed study of the petrogenesis, magma source, and tectonic setting of the mineralization causative granodiorite porphyry. The new data indicate that the granodiorite porphyry is characterized by high SiO₂ (68.21–70.41 wt.%) and Al₂O₃, relatively high K₂O, low Na₂O, and low MgO and CaO concentrations, and is high-K calc-alkaline and peraluminous. The granodiorite porphyry has low Mg^# (38–46) values that are indicative of no interaction between the magmas and the mantle. The samples that we have examined have low Nb/Ta (9.17–10.3) and Rb/Sr (0.28–0.39) ratios, which are indicative of crustal-derived magmas. Source region discrimination diagrams indicate that the magmas that formed the granodiorite porphyry were derived from melting of a mixed amphibolite source in the lower crust. The samples have I_Sr values of 0.70954–0.70979, ε_Nd(t) values of − 8.3 to − 7.9, and t_2DM ages ranging from 1644 to 1677 Ma. These indicate that the magmas that formed this intrusion were generated by melting of Mesoproterozoic lower crustal material. Higher K(Rb) contents of the samples indicate that the magma source is high potassium basaltic material in the lower crust, which could be derived from an enriched mantle source. LA-ICP-MS zircon U–Pb dating of the granodiorite porphyry yields a late Indosinian age (concordia age of 227 ± 1 Ma; MSWD = 0.31), which is close to the molybdenite Re–Os isochron age (227.2 ± 1.9 Ma), indicating further the close relationship between the granodiorite porphyry and the Cu–(Mo) mineralization. These samples are LREE and LILE (e.g., Rb, K, Ba, and Sr) enriched, and HFSE (e.g., Nb, Ta, P, and Ti) depleted, especially in P and Ti, similar to the characteristics of volcanic arc magmas. This intrusion most likely formed during the later stage of Indosinian deep subduction of oceanic slab. This was associated with underplating of mantle-derived magmas, which provided heat for crustal melting. Similar to the Jiadanggen granodiorite porphyry, Indosinian hypabyssal intermediate-felsic intrusive rocks, formed under subduction tectonism or a transitional regime from subduction to syn-collision, make up the most important targets for porphyry Cu(Mo) deposits in the Eastern Kunlun metallogenic belt.     

Phanerozoic amalgamation of the Alxa Block and North China Craton: Evidence from Paleozoic granitoids,U–Pb geochronology and Sr–Nd–Pb–Hf–O isotope geochemistry

The North China Craton (NCC) has been considered to be part of the supercontinent Columbia. The nature of the NCC western boundary, however, remains strongly disputed. A key question in this regard is whether or not the Alxa Block is a part of the NCC. It is located in the vicinity of the inferred boundary, and therefore could potentially resolve the issue of the NCC's relationship to the Columbia supercontinent. Some previous studies based on the Alxa Block's geological evolution and detrital zircon ages suggested that it is likely not a part of the NCC. The lack of evidence from key igneous rock units, however, requires further constraints on the tectonic affinity of the western NCC and Alxa Block and on the timing of their amalgamation.In this study, new zircon U–Pb age and Hf–O isotopes and whole-rock geochemical and Sr–Nd–Pb isotopic data for the Paleozoic granitoids in or near the eastern Alxa Block were used to constrain the petrogenesis of these rocks and the relationship between the Alxa Block and NCC. Secondary ion mass spectrometry (SIMS) U–Pb zircon dating indicates that the Bayanbulage, Hetun, Diebusige and South Diebusige granitoids were formed at ca. 423 Ma, 345 Ma, 345 Ma and 337 Ma, respectively. The Late Silurian (Bayanbulage) quartz diorites have variable SiO₂ (58.0–67.9 wt.%), and low Sr/Y (20–24) values, while the Early Carboniferous (Hetun, Diebusige and South Diebusige) monzogranites have high SiO₂ (71.5–76.7 wt.%) and Sr/Y (40–94) values. The Late Silurian quartz diorites display relatively homogeneous and high zircon δ¹⁸O (8.5–9.1‰) and ε_Hf(t) (− 8.6 to − 5.3) values, high whole-rock ε_Nd(t) values (− 9.2 to − 7.6) and highly radiogenic Pb isotopes (²⁰⁶Pb/²⁰⁴Pb = 18.13–18.25), whereas the Early Carboniferous monzogranites exhibit relatively low and variable zircon δ¹⁸O (5.7–7.2‰) and ε_Hf(t) (− 23.1 to − 7.4) values, low whole-rock initial ⁸⁷Sr/⁸⁶Sr (0.7043–0.7070) and ε_Nd(t) (− 19.1 to − 13.5) values and variable Pb isotopes (²⁰⁶Pb/²⁰⁴Pb = 16.06–18.22). The differences in whole rock Nd model ages and Pb isotope compositions of the Paleoproterozoic–Permian rocks in either side of the west fault of the Bayanwulashan–Diebusige complexes suggest that the Alxa Block is not a part of the NCC, and that the western boundary of the NCC is probably located on this fault. Furthermore, the linear distribution of the Early Paleozoic–Early Carboniferous granitoids, the high zircon δ¹⁸O values of the Late Silurian quartz diorites, the Early Devonian metamorphism and the foreland basin system formed during the collision between the Alxa Block and the NCC indicate that a Paleozoic cryptic suture zone likely existed in this area and records the amalgamation of the Alxa Block and North China Craton. Together with detrital zircon data, the initial collision was considered to have possibly occurred in Late Ordovician.     

Geochronology and geochemistry of the Wunugetushan porphyry Cu–Mo deposit in NE china,and their geological significance

The Wunugetushan porphyry Cu–Mo deposit is located in the Manzhouli district of NE China, on the southern margin of the Mesozoic Mongol–Okhotsk Orogenic Belt. Concentric rings of hydrothermal alteration and Cu–Mo mineralization surround an Early–Middle Jurassic monzogranitic porphyry. The Cu–Mo mineralization is clearly related to the quartz–potassic and quartz–sericite alteration. Molybdenite Re–Os and groundmass ⁴⁰Ar/³⁹Ar of the host porphyry dates indicate that the ore-formation and porphyry-emplacement occurred at 177.6 ± 4.5 Ma and 179.0 ± 1.9 Ma, respectively. Geochemically, the host porphyry of the deposit is characterized by strong LREE/HREE fractionation, enrichment in LILE, Ba, Rb, U, Th and Pb, and depletion of HFSE, Nb, Ta, Ti and HREE. The Sr–Nd–Pb isotopic compositions of the porphyry display an varied initial (⁸⁷Sr/⁸⁶Sr)_i ratio, a positive ε_Nd(t) values and high ²⁰⁶Pb/²⁰⁴Pb_t, ²⁰⁷Pb/²⁰⁴Pb_t and ²⁰⁸Pb/²⁰⁴Pb_t ratios. These data indicate that the magmatic source of the host porphyry comprised two end-members: lithospheric mantle metasomatized by fluids derived from the subducted slab; and continental crust. We infer that the primitive magma of the host porphyry was derived from crust–mantle transition zone. Based on regional geology and geochemistry of the host porphyry, the Wunugetushan deposit is suggested to form in a continental collision environment after closure of the Mongol–Okhotsk Ocean.     

Mesozoic magmatism and metallogenesis associated with the destruction of the North China Craton: Evidence from U–Pb geochronology and stable isotope geochemistry of the Mujicun porphyry Cu–Mo deposit

The North China Craton (NCC) provides a classic example of lithospheric destruction and refertilization. The timing and duration of magmatism and related metallogenesis associated with the destruction process are pivotal to understanding the geodynamic controls. In this study, we present zircon U–Pb and Hf data, Re–Os ages, and He, Ar, Pb and S isotope data from the Mujicun porphyry Cu–Mo deposit in the northern Taihang Mountains within the Central Orogenic Belt of the NCC. We constrain the timing of magmatism as 144.1 ± 1.2 Ma from zircon U–Pb data on the diorite porphyry that hosts Cu–Mo mineralization. Another U–Pb age of 139.7 ± 1.4 Ma was obtained from an epidote skarn that is located in the contact zone between the porphyry and its wall rocks. These data and five Re–Os molybdenite ages that range from 142.7 ± 2.0 Ma to 138.5 ± 1.9 Ma suggest that magmatism and mineralization occurred in about five million year duration from ~ 143 Ma to ~ 138 Ma. The He, Ar, Pb and, Hf data suggest that magmatism involved recycled Neoarchean lower crustal components, with input of heat and volatiles from an upwelling mantle. The Mujicun porphyry and associated mineralization provide a typical example for magmatism and metallogeny associated with lithospheric thinning in the NCC.     

Petrography and geochemistry of Paleocene–Eocene limestones in the Ching-dar syncline, eastern Iran

The Ching-dar syncline is located to the west of the city of Birjand, in the east of han. The ca. 500 m thick studied section at the eastern flank of the syncline contains a sequence of almost continuous shallow- marine limestones that exhibit no major sedimentary breaks or evidence for volcanic activity. Skeletal grains consist of large benthic foraminifera and green algae whereas non-skeletal grains are mostly peloids and intraclasts. They were deposited on a shallow-marine carbonate ramp. The limestones have undergone extensive diagenetic processes with varying intensities, the most important of which are micritization, cementation, compaction （chemical and mechanical）, internal filling and stylolitization. Chemical analysis of the limestone samples revealed high calcium and low magnesium content. Major and minor element values were used to determine the original carbonate mineralogy of these lime- stones. Petrographic evidence and elemental values indicate that calcite was the original carbonate mineral in the limestones of the Ching-dar syncline. The elemental composition of the Ching-dar car- bonates also demonstrates that they have stabilized in a meteoric phreatic environment. Variation of Sr/ Ca vs. Mn values suggests that diagenetic alteration occurred in an open geochemical system.     

The genesis of the ores and intrusions at the Yuhai Cu–Mo deposit in eastern Tianshan,NW China: Constraints from geology,geochronology, geochemistry,and Hf isotope systematics

The Yuhai porphyry Cu–Mo deposit is located in the eastern Tianshan orogenic belt of the southern Central Asian Orogen Belt, being an economically important porphyry Cu deposit in NW China. The deposit comprises sixteen buried orebodies that are predominantly associated with dioritic and granodioritic intrusions and are structurally controlled by roughly NE-trending faults. LA-ICP-MS zircon U–Pb dating yielded crystallization ages of 441.6 ± 2.5 Ma (MSWD = 0.03, n = 24) for diorite and 430.4 ± 2.9 Ma (MSWD = 0.04, n = 19) and 430.3 ± 2.6 Ma (MSWD = 0.09, n = 24) for granodiorite. In situ zircon Hf isotope data on a diorite sample show ε_Hf(t) values from + 8.7 to + 18.6, and two granodiorite samples exhibit similar ε_Hf(t) values from + 12.6 to + 19.6 and + 12.6 to + 18.9, respectively. The dioritic and granodioritic intrusions belong to a low-K tholeiite series and are relatively enriched in large ion lithophile elements (K, Ba, Pb, and Sr) and are depleted in high field strength elements (Th, Nb, Ta, and Ti). Moreover, these intrusions have high SiO₂, Al₂O₃ and MgO contents, low Na₂O, P₂O₅ and TiO₂ contents, low Nb/Ta ratios, and slightly positive Eu anomalies. Re–Os dating of molybdenite intergrowth with chalcopyrite yielded a well-constrained ¹⁸⁷Re–¹⁸⁷Os isochron age of 351.7 ± 2.9 Ma (MSWD = 1.5) with a weighted average age of 355.7 ± 2.4 Ma (MSWD = 0.69) Ma, indicating that the Yuhai Cu–Mo deposit is younger than the intrusion of the diorite and granodiorite. Combined with the regional geological history and above-mentioned data, we suggest that the Yuhai intrusions were most likely derived from the partial melting of mantle components that were previously metasomatized by slab melts formed by the northward subduction of the ancient Tianshan ocean plate beneath the Dananhu–Tousuquan island arc during the Silurian to Carboniferous. Under the subduction-related tectonic setting, the metasomatized mantle magma was emplaced into the shallow crust and induced the formation of the Early Carboniferous Yuhai Cu–Mo deposit, and the hydrothermal fluids of enriched sulfides probably played an important role in the Cu–Mo mineralization.     

Sr–Nd isotope geochemistry of the early Precambrian sub-alkaline mafic igneous rocks from the southern Bastar craton, Central India

Sr–Nd isotope data are reported for the early Precambrian sub-alkaline mafic igneous rocks of the southern Bastar craton, central India. These mafic rocks are mostly dykes but there are a few volcanic exposures. Field relationships together with the petrological and geochemical characteristics of these mafic dykes divide them into two groups; Meso-Neoarchaean sub-alkaline mafic dykes (BD1) and Paleoproterozoic (1.88 Ga) sub-alkaline mafic dykes (BD2). The mafic volcanics are Neoarchaean in age and have very close geochemical relationships with the BD1 type. The two groups have distinctly different concentrations of high-field strength (HFSE) and rare earth elements (REE). The BD2 dykes have higher concentrations of HFSE and REE than the BD1 dykes and associated volcanics and both groups have very distinctive petrogenetic histories. These rocks display a limited range of initial ¹⁴³Nd/¹⁴⁴Nd but a wide range of apparent initial ⁸⁷Sr/⁸⁶Sr. Initial ¹⁴³Nd/¹⁴⁴Nd values in the BD1 dykes and associated volcanics vary between 0.509149 and 0.509466 and in the BD2 dykes the variation is between 0.510303 and 0.510511. All samples have positive ? _Nd values; the BD1 dykes and associated volcanics have ? _Nd values between +0.3 and +6.5 and the BD2 dykes between +1.9 to +6.0. Trace element and Nd isotope data do not suggest severe crustal contamination during the emplacement of the studied rocks. The positive ? _Nd values suggest their derivation from a depleted mantle source. Overlapping positive ? _Nd values suggest that a similar mantle source tapped by variable melt fractions at different times was responsible for the genesis of BD1 (and associated volcanics) and BD2 mafic dykes. The Rb–Sr system is susceptible to alteration and resetting during post-magmatic alteration and metamorphism. Many of the samples studied have anomalous apparent initial ⁸⁷Sr/⁸⁶Sr suggesting post-magmatic changes of the Rb–Sr system which severely restricts the use of Rb–Sr for petrogenetic interpretation.     

Petrogenesis of the Nanling Mountains granites from South China: Constraints from systematic apatite geochemistry and whole-rock geochemical and Sr–Nd isotope compositions

The widespread Mesozoic granitoids in South China (∼135,300 km²) were emplaced in three main periods: Triassic (16% of the total surface area of Mesozoic granitoids), Jurassic (47%), and Cretaceous (37%). Though much study has been conducted on the most abundant Jurassic Nanling Mountains (NLM) granites, their rock affinities relative to the Triassic Darongshan (DRS) and Cretaceous Fuzhou–Zhangzhou Complex (FZC) granites which are typical S- and I-type, respectively, and the issue of their petrogenetic evolution is still the subject of much debate. In this study, we discuss the petrogenesis of NLM granites using apatite geochemistry combined with whole-rock geochemical and Sr–Nd isotope compositions. Sixteen apatite samples from six granite batholiths, one gabbro, and three syenite bodies in the NLM area were analyzed for their major and trace element abundances and compared with those collected from DRS (n = 7) and FZC (n = 6) granites. The apatite geochemistry reveals that Na, Si, S, Mn, Sr, U, Th concentrations and REE distribution patterns for apatites from DRS and FZC granites basically are similar to the S and I granite types of the Lachlan Fold Belt (Australia), whereas those from NLM granites have intermediate properties and cannot be correlated directly with these granite types. According to some indications set by the apatite geochemistry (e.g., lower U and higher Eu abundances), NLM apatites appear to have formed under oxidizing conditions. In addition, we further found that their REE distribution patterns are closely related to aluminum saturation index (ASI) and Nd isotope composition, rather than SiO₂ content or degree of differentiation, of the host rock. The majority of apatites from NLM granites (ASI = 0.97–1.08 and εNd(T) = −8.8 to −11.6) display slightly right-inclined apatite REE patterns distinguishable from the typical S- and I-type. However, those from few granites with ASI > 1.1 and εNd(T) < −11.6 have REE distribution patterns (near-flat) similar to DRS apatites whereas those from granites with ASI < 1.0 and εNd(T) > −6.6 and gabbro and syenite are similar to FZC apatites (strongly right-inclined). In light of Sr and Nd isotope compositions, magmas of NLM intrusives, except gabbro and syenite, and few granites with εNd(T) > −8, generally do not involve a mantle component. Instead, they fit with a melt derived largely from in situ melting or anatexis of the pre-Mesozoic (mainly Caledonian) granitic crust with subordinate pre-Yanshanian (mainly Indosinian) granitic crust. We suggest that an application, using combined whole-rock ASI and εNd(T) values, is as useful as the apatite geochemistry for recognizing possible sources for the NLM granites.     

Geochronology,geochemistry, and mineralization of the granodiorite porphyry hosting the Matou Cu–Mo (±W) deposit,Lower Yangtze River metallogenic belt,eastern China

Porphyry and skarn Cu–Fe–Au–Mo deposits are widespread in the Middle and Lower Yangtze River metallogenic belt (MLYMB), eastern China. The Matou deposit has long been regarded as a typical Cu–Mo porphyry deposit within Lower Yangtze part of the belt. Recently, we identified scheelite and wolframite in quartz veins in the Matou deposit, which is uncommon in other porphyry and skarn deposits in the MLYMB. We carried out detailed zircon U–Pb dating and geochemical and Sr–Nd–Hf isotopic studies of the granodiorite porphyry at Matou to define any differences from other ore-related granitoids. The porphyry shows a SiO₂ content ranging from 61.85 wt.% to 65.74 wt.%, K₂O from 1.99 wt.% to 3.74 wt.%, and MgO from 1.74 wt.% to 2.19 wt.% (Mg^# value ranging from 45 to 55). It is enriched in light rare earth elements and large ion lithophile elements, but relatively depleted in Nb, Ta, Y, Yb and compatible trace elements (such as Cr, Ni, and V), with slight negative Eu anomalies (Eu/Eu^* = 0.88–0.98) and almost no negative Sr anomalies. Results of electron microprobe analysis of rock-forming silicate minerals indicate that the Matou porphyry has been altered by an oxidized fluid that is rich in Mg, Cl, and K. The samples show relatively low ε_Nd(t) values from −7.4 to −7.1, slightly high initial ⁸⁷Sr/⁸⁶Sr values from 0.708223 to 0.709088, and low ε_Hf(t) values of zircon from −9.0 to −6.5, when compared with the other Cu–Mo porphyry deposits in the MLYMB. Zircon U–Pb dating suggests the Matou granodiorite porphyry was emplaced at 139.5 ± 1.5 Ma (MSWD = 1.8, n = 15), which is within the age range of the other porphyries in the MLYMB. Although geochemical characteristics of the Matou and other porphyries in the MLYMB are similar and all adakitic, the detrital zircons in the samples from Matou suggest that Archean lower crust (2543 ± 29 Ma, MSWD = 0.25, n = 5) was involved with the generation of Matou magma, which is different from the other porphyries in the belt. Our study suggests that the Matou granodiorite porphyry originated from partial melting of thickened lower crust that was delaminated into the mantle, similar to the other porphyries in the MLYMB, but it has a higher proportion of lower crustal material, including Archean rocks, which contributed to the formation of the porphyry and related W-rich magmatic-hydrothermal system.     

Origin of the Maoduan Pb–Zn–Mo deposit, eastern Cathaysia Block, China: geological, geochronological, geochemical, and Sr–Nd–Pb–S isotopic constraints

The Maoduan Pb–Zn–Mo deposit is in hydrothermal veins with a pyrrhotite stage followed by a molybdenite and base metal stage. The Re–Os model ages of five molybdenite samples range from 138.6 ± 2.0 to 140.0 ± 1.9 Ma. Their isochron age is 137.7 ± 2.7 Ma. Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) zircon U–Pb dating of the nearby exposed Linggen granite porphyry gave a ²⁰⁶Pb/²³⁸U age of 152.2 ± 2.2 Ma and the hidden Maoduan monzogranite yielded a mean of 140.0 ± 1.6 Ma. These results suggest that the intrusion of the Maoduan monzogranite and Pb–Zn–Mo mineralization are contemporaneous. δ ³⁴S values of sulfide minerals range from 3.4‰ to 4.8‰, similar to magmatic sulfur. Four sulfide samples have ²⁰⁶Pb/²⁰⁴Pb = 18.252–18.432, ²⁰⁷Pb/²⁰⁴Pb = 15.609–15.779, and ²⁰⁸Pb/²⁰⁴Pb = 38.640–39.431, similar to the age-corrected data of the Maoduan monzogranite. These isotope data support a genetic relationship between the Pb–Zn–Mo mineralization and the Maoduan monzogranite and probably indicate a common deep source. The Maoduan monzogranite has geochemical features similar to highly fractionated I-type granites, such as high SiO₂ (73.7–75.2 wt.%) and alkalis (K₂O + Na₂O = 7.8–8.9 wt.%) and low FeO_t (0.8–1.3 wt.%), MgO (~0.3 wt.%), P₂O₅ (~0.03 wt.%), and TiO₂ (~0.2 wt.%). The granitic rocks are enriched in Rb, Th, and U but depleted in Ba, Sr, Nb, Ta, P, and Ti. REE patterns are characterized by marked negative Eu anomalies (Eu/Eu^* = 0.2–0.4). The Maoduan monzogranite, having (⁸⁷Sr/⁸⁶Sr) _t  = 0.7169 to 0.7170 and ε_Nd(t) = −13.8 to −13.7, was probably derived from mixing of partial melts from enriched mantle and the Paleoproterozoic Badu group in an extensional tectonic setting.     

Geology,mineralogy, and sulfur isotope geochemistry of the Sargaz Cu–Zn volcanogenic massive sulfide deposit,Sanandaj–Sirjan Zone,Iran

The Sargaz Cu–Zn massive sulfide deposit is situated in the southeastern part of Kerman Province, in the southern Sanandaj–Sirjan Zone of Iran. The stratigraphic footwall of the Sargaz deposit is Upper Triassic to Lower Jurassic (?) pillowed basalt, whereas the stratigraphic hanging wall is andesite. Mafic volcanic rocks are overlain by andesitic volcaniclastics and volcanic breccias and locally by heterogeneous debris flows. Rhyodacitic flows and volcaniclastics overlie the sequence of basaltic and andesitic rocks. Based on the bimodal nature of volcanism, the regional geologic setting and petrochemistry of the volcanic rocks, we suggest massive sulfide mineralization in the Sargaz formed in a nascent ensialic back-arc basin. The current reserves (after ancient mining) of the Sargaz deposit are 3 Mt at 1.34% Cu, 0.38% Zn, 0.08%Pb, 0.24 g/t Au, and 7 g/t Ag. The structurally dismembered massive sulfide lens is zoned from a pyrite-rich base, to a pyrite?±?chalcopyrite-rich central part, and a sphalerite–chalcopyrite-rich upper part, with a sphalerite-rich zone lateral to the upper part. The main sulfide mineral is pyrite, with lesser chalcopyrite and sphalerite. The feeder zone, comprised of a vein stockwork consists of quartz–sulfide–sericite pesudobreccia and, in the deepest part, chlorite–quartz–pyrite pesudobreccia. Footwall hydrothermal alteration extends at least 70–80 m below the massive sulfide lens and more than a hundred meters along strike from the massive sulfide lens. Jasper and Fe–Mn bearing chert horizons lateral to the sulfide deposit represent low-temperature hydrothermal precipitates of the evolving hydrothermal system. Based on mineral textures and paragenetic relationships, the growth history of the Sargaz deposit is complex and includes: (1) early precipitation of sulfides (protore) on the seafloor as precipitation of fine-grained anhedral pyrite, sphalerite, quartz, and barite; (2) anhydrite precipitation in open spaces and mineral interstices within the sulfide mound followed by its subsequent dissolution, formation of breccia textures, and mound clasts and precipitation of coarse-grained pyrite, sphalerite, tetrahedrite–tennantite, galena and barite; (3) replacement of pre-existing sulfides by chalcopyrite precipitated at higher temperatures (zone refining); (4) continued “refining” led to the dissolution of stage 3 chalcopyrite and formation of a base-metal-depleted pyrite body in the lowermost part of the massive sulfide lens; (5) carbonate veins were emplaced into the sulfide lens, replacing stage 2 barite. The δ³⁴S composition of the sulfides ranges from +2.8‰ to +8.5‰ (average, +5.6‰) with a general increase of δ³⁴S ratios with depth within the massive sulfide lens and underlying stockwork zone. The heavier values indicate that some of the sulfur was derived from seawater sulfate that was ultimately thermochemically reduced in deep hydrothermal reaction zones.