Geochronology–geochemistry of the Cida bimodal intrusive complex,central Emeishan large igneous province,southwest China: petrogenesis and plume–lithosphere interaction

The Cida complex is situated in the Panxi region and is predominantly composed of mafic-ultramafic and syenitic rock units; minor amounts of intermediate rocks occupy the contact zone between the two major rock types. The intermediate unit is mineralogically heterogeneous and typically exhibits a mottled structure. Laser ablation–inductively coupled plasma–mass spectrometry (LA–ICP–MS) U–Pb zircon dating shows that the mafic-ultramafic rocks and syenitic rocks formed almost coevally (243 ± 0.77 Ma and 240.5 ± 0.76 Ma, respectively). These ages may represent the end phase of the Emeishan large igneous province (ELIP) magmatism. Most of these three rock types possess alkaline and metaluminous affinities. The mafic-ultramafic, syenitic, and intermediate units have K₂O + Na₂O contents of 1.85–5.16, 6.55–10.46, and 9.55–11.54 wt.%, and SiO₂ contents of 40.06–46.70, 61.74–68.54, and 51.57–54.13 wt.%, respectively. The mafic-ultramafic unit displays ocean-island basalt (OIB)-like primitive-mantle-normalized incompatible element patterns, coupled with low initial ⁸⁷Sr/⁸⁶Sr ratios (0.7048–0.7064), positive ?_Nd(t) (0.32–2.23), and zircon ?_Hf(t) (4.53–14.17) values, consistent with a mafic plume-head origin, whereas one exceptional sample with negative ?_Nd(t) (–0.22) can be interpreted as due to the involvement of considerable amounts of enriched subcontinental lithospheric mantle. The relatively low (La/Yb) _N ratios (3.40–7.69) reflect a spinel-facies lherzolite source. The syenitic unit is characterized by enrichment in large ion lithophile elements (e.g. Rb, K, Pb) and light rare earth elements (LREEs), relative to high field strength elements (e.g. Nb, Ta, P, Ti) and heavy rare earth elements (HREEs), respectively. These features, together with their metaluminous affinities, low SiO₂ contents, lower initial ⁸⁷Sr/⁸⁶Sr ratios (0.7043), positive ?_Nd(t) (0.18), and zircon ?_Hf(t) (2.63–10.09) values as well as modelling of REEs, can be plausibly explained by crustal partial melting of juvenile basic materials beneath the Yangtze Block. In contrast, the field, petrographic observations, and geochemical signatures (e.g. the linear correlations between FeO* and MgO, K/Ba and Rb/Ba ratios) suggest that the intermediate unit may have resulted from magma mixing between the syenitic and basaltic magmas that in turn had evolved from a parental mafic-ultramafic liquid. Thus, the formation of the Cida complex can be attributed to the plume–lithosphere interaction plus partial melting of juvenile basic lower crust in response to heating of underplated plume-derived basaltic magma.     

Platinum-group elemental chemistry of the Baima and Taihe Fe–Ti oxide bearing gabbroic intrusions of the Emeishan large igneous province,SW China

Nickel-, copper-, and platinum group element (PGE)-enriched sulphide mineralization in large igneous provinces has attracted numerous PGE studies. However, the distribution and behavior of PGEs as well as the history of sulphide saturation are less clear in oxide-dominated mineralization. Platinum group elements of oxide-bearing layered mafic intrusions from the Emeishan large igneous province are examined in this study. Samples collected from the Baima and Taihe oxide-bearing layered gabbroic intrusions reveal contrasting results. The samples from Baima gabbroic rocks have low total PGE abundances (ΣPGE < 4 ppb) whereas the Taihe gabbroic rocks, on average, have more than double the concentration but are variable ranging from ΣPGE < 2 ppb to ΣPGE ∼300 ppb. The Baima gabbro is platinum-subgroup PGE (PPGE = Rh, Pt and Pd) enriched and iridium-subgroup PGE (IPGE = Os, Ir and Ru) depleted, with a distinct positive Ru anomaly on a primitive mantle normalized multi-element plot. The Taihe gabbros are also PPGE enriched but with negative Ru and Pd anomalies on a primitive mantle normalized multi-element plot. The PGE concentrations of Baima rocks are indicative of fractionation of a relatively evolved, mafic, S-undersaturated parental magma that was affected by earlier sulphide segregation. In contrast, the Taihe rocks record evidence of both S-saturated and S-undersaturated conditions and that the parental magma was likely emplaced very close to S-saturation. Comparisons of the platinum group element contents in the Emeishan flood basalts and the Emeishan oxide-bearing intrusions suggest that the PGE budget in a magma is not controlled by magma series (high-Ti vs. low-Ti), but very much by crustal contamination. The unlikelihood of substantial crustal contamination in the Taihe magma allowed the magma to remain S-undersaturated for a longer duration. PGE and sulphide mineralization was not identified in the Taihe intrusion but the presence of one PGE-enriched sample (Pt + Pd = ∼300 ppb) suggests that the parental magma likely did not experience sulphide segregation and is a potential target for further prospecting.     

Geochronology and geochemistry of the Nantianwan mafic–ultramafic complex,Emeishan large igneous province: metallogenesis of magmatic Ni–Cu sulphide deposits and geodynamic setting

The Nantianwan mafic–ultramafic complex is situated in the northwest part of the Panxi district, southwest China. It consists predominantly of gabbros, gabbronorites, and lherzolites. LA–ICP–MS U–Pb zircon dating of the gabbronorites yields an age of 259.7 ± 0.6 million years, consistent with the ages of other mafic–ultramafic intrusions in the Emeishan large igneous province (ELIP). Gabbronorites and lherzolites host Cu–Ni sulphide ores. Cumulus texture is pronounced in these rocks, containing magnesium-rich olivine (up to 81.4% forsterite). SiO₂ contents of the lherzolites range from 42.93 to 44.18 wt.%, whereas those of the gabbronorites vary between 44.89 and 52.76 wt.%. Analysed samples have low rare earth element (REE) contents (23.22–30.16 ppm for lherzolites and 25.21–61.05 ppm for gabbronorites). Both lherzolites and gabbronorites have similar chondrite-normalized REE patterns, suggesting that they are comagmatic. All samples are slightly enriched in large ion lithophile elements (LILEs, e.g. Rb, Ba, and Sr) relative to high field strength elements (HFSEs, e.g. Nb, Ta, and Ti), very similar to those of ocean island basalts (OIBs). The presence of cumulus textures and geochemical signatures indicates that fractional crystallization played an important role in the petrogenesis of these rocks. Initial (⁸⁷Sr/⁸⁶Sr) _t (t?=?260 Ma) ratios and ?_Nd(t) values of the mafic–ultramafic suite vary from 0.70542 to 0.70763, and??0.4 to 1.7, respectively. Compared to the Cu–Ni-bearing Baimazhai and Limahe intrusions in the ELIP, which were considerably contaminated by variable crustal materials, the Nantianwan complex exhibits much lower (⁸⁷Sr/⁸⁶Sr) _t . Their ?_Nd(t) versus (Th/Nb)_PM ratios also indicate that the ore-bearing magmas did not undergo significant crustal contamination. In combination with (Tb/Yb)_PM versus (Yb/Sm)_PM modelling, we infer that the magmas originated from an incompatible elements-enriched spinel-facies lherzolite that itself formed by interaction between the Emeishan plume and the lithospheric mantle. Most plots of NiO versus Fo contents of olivine suggest that sulphides are separated from the parental magma by liquid immiscibility, which is also supported by bulk-rock Cu/Zr ratios of the lherzolites (7.04–102.67) and gabbronorites (0.88–5.56). We suggest that the gabbronorites and lherzolites experienced undersaturation to oversaturation of sulphur; the latter may be due to fractional crystallization in a high-level magma chamber, accounting for the sulphide segregation.     

Petrology,geochemistry and zircon U–Pb and Lu–Hf isotopes of the Cretaceous dykes in the central North China Craton: Implications for magma genesis and gold metallogeny

The Trans-North China Orogen (TNCO), a Paleoproterozoic suture that amalgamates the Western and Eastern Blocks of the North China Craton (NCC), witnessed extensive magmatism and metallogeny during Mesozoic, associated with intraplate tectonics and differential destruction of the cratonic lithosphere. Here we investigate a suite of porphyry dykes surrounding the Mapeng batholith in the Fuping Complex within the TNCO in relation to the Mesozoic gold and molybdenum mineralization. The major element chemistry of these dykes show a range of SiO₂ (57.92 to 69.47 wt.%), Na₂O (3.20 to 4.77 wt.%), K₂O (3.12 to 4.60 wt.%) and MgO (0.51 to 3.67 wt.%), together with high concentration of LREE and LILE, and relatively low contents of HREE and HFSE. The rocks display (La/Yb)_N = 13.53–48.11, negative Nb, Ta, Th, U and Zr anomalies, and distinctly positive Ba, K and Sm anomalies. The mineralogy and geochemistry of the porphyry dykes indicate the rocks to be high-K calc-alkaline, and I-type, with adakitic features similar to those of the adjacent Mapeng batholith. The source magma for these rocks was derived from a mixture of reworked ancient continent crust and juvenile mantle materials. The zircon U–Pb data from these rocks show ages in the range of 124 to 129 Ma, broadly coinciding with the emplacement age of the Mapeng intrusion. The inherited zircons of ca. 2.5, 2.0 and 1.8 Ga in the dykes represent capture from the basement rocks during melting. The zircon Lu–Hf isotopic compositions show negative ε_Hf(t) values varying from − 27.8 to − 11.3, with Hf depleted model ages (t_DM) ranging from 1228 Ma to 1918 Ma and Hf crustal model ages (t_DM^C) of 1905 Ma to 2938 Ma, suggesting that the Mesozoic magmatism and associated metallogeny involved substantial recycling of ancient basement rocks of the NCC. We present an integrated model to evaluate the genesis of the porphyry systems and their relation to mineralization. We envisage that these dykes probably acted as stoppers (impermeable barriers) that prevented the leakage and run-off of the ore-bearing fluids, and played a key role in concentrating the gold and molybdenum mineralization.     

Late Jurassic Sn metallogeny in eastern Guangdong,SE China coast: Evidence from geochronology,geochemistry and Sr–Nd–Hf–S isotopes of the Dadaoshan Sn deposit

The newly discovered Dadaoshan Sn deposit is located in the eastern Guangdong Sn–W province, coastal SE China. The Sn mineralization, hosted in Jurassic porphyritic granite and the Lower Jurassic Jinji Formation sedimentary wall rocks, is considered to be granite-related. In this study, the porphyritic granite was LA–ICP–MS zircon U–Pb dated to be 153.2 ± 1.2 Ma, consistent with the syn-mineralization molybdenite Re–Os age of 152.6 ± 1.8 Ma. The porphyritic granite samples are weakly peraluminous (A/CNK = 1.0–1.1) and high-K calc-alkaline. The rocks contain high SiO₂ (72.9–75.6 wt%), moderate Rb/Sr (5–9) and low ΣREE (136–223 ppm). They are enriched in F, Li, Rb and Sn, depleted in Ba, Sr, P, Zr, Th, Nb and Y, and have distinct negative Eu anomalies (δEu = 0.09–0.18), suggesting that the porphyritic granite is highly fractionated I-type granite. The calculated initial ⁸⁷Sr/⁸⁶Sr (0.711582–0.715173), relatively low ɛ_Nd(t) (−9.48 to −8.54; T_DM2 = 1638–1814 Ma), and the zircon ε_Hf(t) (−14.2 to −5.1; two-stage model ages = 1528–2103 Ma) all suggest that the granite was mainly crustal-derived with little mantle input. Sulfur isotopic compositions for the sulfides (arsenopyrite and chalcopyrite: δ³⁴S = −1.1 to 1.4‰, average = −0.1) imply a dominantly magmatic sulfur source. The calculated zircon Ce⁴⁺/Ce³⁺ and Eu_N/Eu_N¹ ratios of the Dadaoshan granite range from 1.0 to 112 (mean = 31.7) and from 0.04 to 0.37 (mean = 0.14), respectively, indicating a low oxygen fugacity for the magma. The reducing and highly fractionated nature of the Dadaoshan granitic magma may have played a key role in the Sn mineralization.It was previously argued that the Jurassic Sn–W mineralization and its causative magmatism were largely confined in the South China interior, e.g., the Nanling Range. Our new data suggest that the Late Jurassic Sn–W mineralization and its causative magmatism actually extended to the SE China coastal area. The Dadaoshan granite may have been generated from partial crustal melting led by underplating of mantle-derived magmas in an extensional environment. Regional extension may have been related to the west-directed, flat-slab subduction and delamination of the Paleo-Pacific (Izanagi) plate beneath the South China block. Another suite of Early Cretaceous Sn–W-bearing granitic rocks in eastern Guangdong may have mainly been crustal-derived with minor mantle input, and likely occurred under back-arc extensional setting led by the Paleo-Pacific subduction rollback.     

Stable isotopes and noble gases in the Xishimen gold deposit,central North China Craton: metallogeny associated with lithospheric thinning and crust–mantle interaction

Quartz-vein type gold mineralization at Xishimen is a recently discovered gold deposit in the central North China Craton. More than 50 auriferous quartz veins occur in this region within a NNW–SSE-trending fault zone 4600 m in length and 3–10 m wide. Wall rocks are mainly Precambrian tonalite–trondhjemite–granodiorite (TTG) gneisses and associated supracrustals, modified by K-feldspathization and pyrite-phyllic hydrothermal alteration. Based on detailed field and petrographic studies, we identify five episodes of mineralization: pyrite-phyllic stage (I), coarse-grained pyrite-milky white quartz stage (II), fine-grained smoky grey quartz-pyrite stage (III), fine-grained smoky grey quartz-polymetallic sulphide stage (IV), and quartz-carbonate stage (V). We present results of δ³⁴S analysis of sulphide minerals from the different stages which show tightly clustered values in the range of –1.0‰ to 2.1‰, close to those of mantle and meteorite sulphur. Lead isotopic ratios of pyrite from the early to main stages also show restricted ranges with ²⁰⁶Pb/²⁰⁴Pb of 16.289–17.286, ²⁰⁷Pb/²⁰⁴Pb of 15.217–15.453, ²⁰⁸Pb/²⁰⁴Pb of 37.012–38.232, implying lower crustal input. ³He/⁴He and ⁴⁰Ar/³⁶Ar ratios of fluid trapped in pyrite are 0.68 Ra to 1.20 Ra (where Ra is the ³He/⁴He ratio of air = 1.4 × 10^?6) and 540.9–1065, respectively. ³He and ⁴Ar concentrations vary from 10.05 to 18.5 (10^?7 cm³STP/g) and 6.15 to 17.4 (10^?7cm³STP/g), respectively, with calculated mantle helium ranging from 8.47% to 14.96% (average 11.01%). δ¹⁸O_Q and δ¹⁸D_Q values of quartz range from 8.0‰ to 13.2‰ and –101.9‰ to –70.5‰, respectively, with calculated δ¹⁸O_W values of the mineralizing fluid ranging from 1.11‰ to 5.72‰, suggesting the mixing of magmatic aqueous fluid with meteoric water during gold precipitation. We correlate the mixed crust–mantle signature of the ore-forming sources to magmatism and metallogeny associated with Mesozoic inhomogeneous lithosphere thinning in the central North China Craton.     

Differentiation, crustal contamination and emplacement of magmas in the formation of the Nantianwan mafic intrusion of the ~260?Ma Emeishan large igneous province, SW China

The Nantianwan mafic intrusion in the Panxi region, SW China, part of the ~260?Ma Emeishan large igneous province, consists of the olivine gabbro and gabbronorite units, separated by a transitional zone. Olivine gabbros contain olivine with Fo values ranging from 83 to 87, indicating crystallization from a moderately evolved magma. They have 0.2 to 0.9?wt?% sulfide with highly variable PGE (17?C151?ppb) and variable Cu/Pd ratios (1,500?C32,500). Modeling results indicate that they were derived from picritic magmas with high initial PGE concentrations. Olivine gabbros have negative ??Nd(t) values (?1.3 to ?0.1) and positive ??Os(t) values (5?C15), consistent with low degrees of crustal contamination. Gabbronorites include sulfide-bearing and sulfide-poor varieties, and both have olivine with Fo values ranging from 74 to 79, indicating crystallization from a more evolved magma than that for olivine gabbros. Sulfide-bearing gabbronorites contain 1.9?C4.1?wt?% sulfide and 37?C160?ppb PGE and high Cu/Pd ratios (54,000?C624,000). Sulfide-poor gabbronorites have 0.1?C0.6?wt?% sulfide and 0.2?C15?ppb PGE and very high Cu/Pd ratios (16,900?C2,370,000). Both sulfide-bearing and sulfide-poor gabbronorites have ??Nd(t) values (?0.9 to ?2.1) similar to those for olivine gabbros, but their ??Os(t) values (17?C262) are much higher and more variable than those of the olivine gabbros. Selective assimilation of crustal sulfides from the country rocks is thus considered to have resulted in more radiogenic ¹⁸⁷Os of the gabbronorites. Processes such as magma differentiation, crustal contamination and sulfide saturation at different stages in magma chambers may have intervened during formation of the intrusion. Parental magmas were derived from picritic magmas that had fractionated olivine under S-undersaturated conditions before entering a deep-seated staging magma chamber, where the parental magmas crystallized olivine, assimilated minor crustal rocks and reached sulfide saturation, forming an olivine- and sulfide-laden crystal mush in the lower part and evolved magmas in the upper part of the chamber. The evolved magmas were forced out of the staging chamber and became S-undersaturated due to a pressure drop during ascent to a shallow magma chamber. The magmas re-attained sulfide saturation by assimilating external S from S-rich country rocks. They may have entered the shallow magma chamber as several pulses so that several gabbronorite layers each with sulfide segregated to the base and a sulfide-poor upper part. The olivine gabbro unit formed from a new and more primitive magma that entrained olivine crystals and sulfide droplets from the lower part of the staging chamber. A transitional zone formed along the boundary with the gabbronorite unit due to chemical interaction between the two rock units.     

Geochronological limits of subalkaline magmatism in the Ket-Kap–Yuna igneous province,Aldan Shield

Comparative U-Pb (zircon- and sphene-based, for the first time) and K-Ar (biotite-, amphibole, and whole rock-based) dating of monzonitoids and subalkaline granitoids of the Ket-Kap and Uchur volcanic-plutonic complexes (Ket-Kap-Yuna Igneous Province is one of the areas of tectonic-magmatic activation of the Aldan Shield), respectively, has been made.     

Ni–Cu–(PGE) magmatic sulfide deposits in the Yangliuping area,Permian Emeishan igneous province,SW China

The Ni–Cu–PGE sulfide deposits in the Yangliuping area, SW China, are hosted in mafic–ultramafic sills. The four mineralized sills are located in the Yangliuping tectonic dome and intrude Devonian carbonaceous marble, graphitic schist. The sills are 200–300 m thick and 1,000–2,000 m in strike length and now consist chiefly of serpentinite, talc schist, tremolite schist, and meta-gabbro. Disseminated Ni–Cu sulfide mineralisation occurs in the serpentinite in the lower parts of the sills. Massive sulfide mineralisation is located in the base of the sills and in the footwall along fractures beneath the mineralized serpentinite. Although the sulfide ores have been modified by hydrothermal activity, there are relict cumulate textures in the disseminated sulfides indicating a magmatic origin for the ores. The Yangliuping Intrusions and the Dashibao Formation have similar primitive-mantle normalized trace element and platinum group element (PGE) patterns, indicating that they are derived from a common parental magma type. The positive correlation between Cu concentrations and Cu/Zr ratios of the Dashibao Formation basalts indicates that the chalcophile elements were removed before eruption. We propose that fractional crystallization of the Yangliuping magma accompanied by the introduction of S and CO₂ from the wall rocks caused the magma to become S-saturated leading to the segregation of magmatic sulfides that became enriched in Ni–Cu–(PGE). The sills acted as conduits for the overlying Dashibao Formation basalts with the sulfide liquid, along with early crystallizing olivine and pyroxene, segregating from the magma as it passed through the conduits prior to eruption.Editorial handling: H.E. Frimmel     

The origin of the Dapingzhang volcanogenic Cu–Pb–Zn ore deposit,Yunnan province,SW China: Constraints from host rock geochemistry and ore Os–Pb–S–C–O–H isotopes

The Dapingzhang volcanogenic Cu–Pb–Zn sulfide deposit is located in the Lancangjiang tectonic zone within the Sanjiang region, Yunnan province of southwestern China. The deposit occurs within a felsic volcanic dome belonging to a mid-Silurian volcanic belt stretching for more than 100 km from Dapingzhang to Sandashan. The mineralized volcanic rocks are predominantly keratophyre and quartz keratophyre with subordinate spilite. The Dapingzhang deposit is characterized by well-developed vertical zonation with stockwork ores in the bottom, disseminated sulfide ores in the middle, and massive sulfide ores in the top, overlain by a thin layer of chemical sedimentary exhalative rocks (chert and barite). The Re–Os age of the pyrites from the deposit is 417 ± 23 Ma, indistinguishable from the age of the associated felsic volcanic rocks. The associated felsic volcanic rocks are characterized by negative Nb–Ta anomalies and positive ε_Nd(t) values (+ 4.4–+6.5), similar to the coeval calc-alkaline volcanic rocks in the region. This observation supports the interpretation that the felsic volcanic rocks associated with the Dapingzhang deposit are the derivatives of arc basaltic magma by extensive fractional crystallization. The δ³⁴S values of the sulfides from the deposit vary from − 1.24 to + 4.32‰, indicating a predominantly magmatic source for the sulfur. The sulfides are also characterized by homogeneous and relatively low radiogenic Pb isotope compositions (²⁰⁶Pb/²⁰⁴Pb = 18.310–18.656, ²⁰⁷Pb/²⁰⁴Pb = 15.489–15.643 and ²⁰⁸Pb/²⁰⁴Pb = 37.811–38.662), similar to the Pb isotopic compositions of the associated volcanic rocks. The Pb isotopic data indicate that mantle-derived Pb is more prevalent than crust-derived Pb in the deposit. The S–Pb isotopic data indicate that the important ore-forming materials were mainly derived from the associated volcanic rocks. The δ¹³C_PDB and δ¹⁸O_SMOW values of the associated hydrothermal calcite crystals vary from − 2.3‰ to + 0.27‰ and from + 14.6 to + 24.4‰, respectively. These values are between the mantle and marine carbonate values. The narrow range of the δ¹³C_PDB values for the calcite indicates that carbon-bearing species in the hydrothermal fluids were primarily derived from marine carbonates. The δ¹⁸O values for the hydrothermal fluids, calculated from the measured values for quartz, are between − 2.1‰ and + 3.5‰. The corresponding δD values for the fluids range from − 59‰ to − 84‰. The O–H isotopic data indicate mixing between magmatic fluids and seawater in the ore-forming hydrothermal system. Similar to a typical volcanogenic massive sulfide (VMS) deposit, the ore-forming fluids contained both magmatic fluids and heated seawater; the ore metals and regents were derived from the underlying magma as well as felsic country rocks.     

Refertilization of serpentinites in the Sulu UHP terrane,Eastern China: constraints from geochronology,mineral composition,geochemistry, and Re–Os isotopes

ABSTRACT

Serpentinites from Junan (JN), Rizhao (RZ), and Rongcheng (RC) in the Sulu ultra-high-pressure (UHP) terrane, China, were analysed for U–Pb zircon geochronology, mineral chemistry, whole-rock major and trace element chemistry (including rare-earth elements (REEs) and platinum-group elements (PGEs)), and Re–Os isotopes, in order to better constrain their petrogenesis and geodynamic process. The serpentinite zircons yield two age groups: 731 ± 10 to 780 ± 10 Ma for relic magmatic zircon cores, which may indicate early crystallization and emplacement of the peridotite in the Yangtze crust, and 209 ± 2 to 218 ± 3 Ma for metamorphic zircon, which coincides with Triassic UHP metamorphism. The spinels in the serpentinites exhibit significant Cr# variation (0.6–0.91) and have undergone multi-stage metamorphism. The serpentinites are characterized by enrichment in incompatible trace elements, low Ni and IPGE concentrations, and high Pd/Ir ratios, and the bulk-rock major elements plot in the ultramafic cumulate region. Their Re and Os concentrations are similar to those of typical orogenic peridotite, but they have high ¹⁸⁷Os/¹⁸⁸Os ratios (0.12433–0.14423). We believe that the serpentinite’s protolith consisted of cumulates from an asthenosphere-derived melt that intruded into the continental crust of the Yangtze craton in the Neoproterozoic. These cumulates were later subducted and metamorphosed during the subduction of the Yangtze craton in the Triassic. The serpentinites underwent melt–rock interactions and fluid enrichment, both prior to and during serpentinization.     

Re–Os geochemistry and geochronology of the Ransko gabbro–peridotite massif, Bohemian Massif

The Ransko gabbro–peridotite massif in Eastern Bohemia is a strongly differentiated intrusive complex, which hosts low-grade Ni–Cu ores mainly developed close to the contact of olivine-rich rocks with gabbros, in troctolites, and to a much lesser extent in both pyroxene and olivine gabbros and plagioclase-rich peridotites. Gabbro, troctolite, peridotite and Ni–Cu ores from the Jezírka Ni–Cu (PGE) deposit, considered to be a typical example of the liquid segregation style of mineralization, were analyzed for Re–Os concentrations and isotopic ratios. Seven barren and mineralized samples from the Jezírka deposit yielded a Re–Os regression of 341.5?±?7.9 Ma (MSWD?=?69). Strongly mineralized peridotite with mantle-like initial ¹⁸⁷Os/¹⁸⁸Os ratio of 0.125 suggests that Os as well as other PGE present in the Ni–Cu mineralization are predominantly of mantle origin. On the other hand, barren and low-mineralized samples have radiogenic initial ¹⁸⁷Os/¹⁸⁸Os ratios of 0.14–0.16 suggesting some import of Re and/or radiogenic ¹⁸⁷Os most likely through contamination by continental crust during magma emplacement. The Re–Os age of the Ransko Massif is significantly younger than the previously suggested Lower Cambrian age, but it is similar to and/or younger than the age of metamorphism of the adjacent Kutná Hora crystalline complex and the Moldanubian unit. Therefore, it is likely that the emplacement of the Ransko massif and its Ni–Cu mineralization was closely connected with the late-stage evolution of the Kutná Hora crystalline complex.     

Lead isotopic systematics for native copperchalcocite mineralization in basaltic lavas of the Emeishan large igneous province, SW China： Implications for the source of copper

The Emeishan continental flood basalt, which is widespread in Yunnan, Guizhou and Sichuan provinces of Southwest China, is the volcanic product of a Permian mantle plume, and native copper-chalcocite mineralization associated with the basalt is very common in the border area of Yunnan and Guizhou provinces. The mineralization occurred in the tuff intercalation and terrestrial sedimentary rock intercalation which were formed during the main period of basalt eruption. The orebodies are controlled by the stratigraphic position and faults. Metal ore minerals in the ores are mainly native copper, chalcocite and tenorite, with small amounts of chalcopyrite, bomite, pyrite and malachite, and sometimes with large amounts of bitumen, carbon and plant debris. Several decades of ore deposits are distributed in the neighboring areas of the two provinces, while most of them are small-scale deposits or only ore occurrences. By comparing the lead isotopic composition of the ores with that of the wall-rocks, cover and basement rocks of various periods, the source of copper in this type of ore deposits was studied in this paper. The results showed that: (1) The Pb isotopic composition of the ores from ten deposits is absolutely different from that of sili-ceous-argillaceus rocks of the Upper Permian Xuanwei Formation, limestones of the Lower Permian Series and Carboniferous, Cambrian sandstone-shale and recta-sedimentary rock and dolomite from the upper part of the Meso-Proterozoic Kunyang Group, This indicates that ore lead was derived neither from the cover rock nor from the basement rocks; (2) Although the Neo-Proterozoic Siman dolomite and silicalite, and dolomite in the lower part of the Kunyang Group are similar in Pb isotopic composition to the ores, lead and copper contents in these rocks are very low and they have not made great contributions to copper mineralization; (3) The ores have the same Pb iso-topic composition as the basalt, the latter being enriched in copper. These facts indicate that lead and copper were derived from the basalt. According to the regional geological data and the geological-geochemical characteristics of the ore deposits, it is suggested that ore-forming materials were leached out from the basalt. The thickness and buried depth of the basalt and regional tectonic dynamics can affect the formation of large-scale copper deposits. Therefore, exploration for this type of ore deposits should be conducted in the areas from western Yunnan to western Sichuan, where there are developed basalts of great thickness, with extensive tectonic movement and magmatic activity.     

Isotopic (C–O–S) geochemistry and Re–Os geochronology of the Haobugao Zn–Fe deposit in Inner Mongolia,NE China

The Haobugao Zn–Fe deposit is a typical skarn deposit located in the southern part of the Great Xing’an Range that hosts polymetallic mineralization over a large region. The main ore minerals at the deposit include sphalerite, magnetite, galena, chalcopyrite and pyrite, and the main gangue minerals include andradite, grossular garnet, hedenbergite, diopside, ilvaite, calcite and quartz. There are broadly two mineralizing periods represented by the relatively older skarn and younger quartz–sulfide veins. In detail, there are five metallogenic stages consisting of an early skarn, late skarn, oxide, early quartz–sulfide, and late quartz–sulfide–calcite stages. Electron microprobe analyses show that the garnet at the deposit varies in composition from And_97.95Gro_0.41Pyr_1.64 to And_30.69Gro_66.69Pyr_2.63, and pyroxene is compositionally in the diopside–hedenbergite range (i.e. Di_90.63Hd_8.00Jo_1.37–Hd_88.98Di_4.53Jo_6.49). Petrographic observations and electron microprobe analyses indicate that the sphalerite has three generations ([Zn_0.93Fe_0.08]S–[Zn_0.75Fe_0.24]S). The Zn associated with the first generation sphalerite replaced Cu and Fe of early xenomorphic granular chalcopyrite (i.e. [Cu_1.01Fe_1.03]S₂–[Cu_0.99Fe_0.99]S₂), and part of the first generation sphalerite is coeval with late chalcopyrite (i.e. [Cu_0.96Fe_0.99Zn_0.03]S₂–[Cu_1.00Fe_1.03Zn_0.01]S₂). Magnetite has a noticeable negative Ce anomaly (δCe = ∼0.17 to 0.54), which might be a result of the oxidized ore-fluid. Thirty δ³⁴S_V-PDB analyses of sulfides from the ore range from −2.3 to −0.1‰ in value, which are indicative of a magmatic source. The δ¹³C‰ and δ¹⁸O‰ values for calcite from the ore formed at quartz–sulfide–calcite stage vary from −9.9 to −5.5‰ and from −4.2 to 1.1‰, respectively, contrasting with δ¹³C‰ (2.9–4.8‰) and δ¹⁸O‰ (9.8–13.9‰) values for calcite from marble. It is suggested that the ore-forming fluid associated with late stage of mineralization was predominantly magmatic in origin with some input of local meteoric water.Molybdenite from the Haobugao deposit defines an isochron age of 142 ± 1 Ma, which is interpreted as the mineralization age being synchronous, within error, with the zircon U–Pb ages of 140 ± 1, 141 ± 2, and 141 ± 1 Ma for granite at the deposit. These data and characteristics of lithology and mineralization further show that the Zn–Fe mineralization is temporally and spatially related to the emplacement of granite in an extensional tectonic setting during the Mesozoic.     

Integration of zircon and apatite U–Pb geochronology and geochemical mapping of the Wude basalts(Emeishan large igneous province):A tool for a better understanding of the tectonothermal and geodynamic evolution of the Emeishan LIP

Radiogenic isotopic dating and Lu–Hf isotopic composition using laser ablation-inductively coupled plasma-mass spectrometry(LA-ICP-MS)of the Wude basalt in Yunnan province from the Emeishan large igneous province(ELIP)yielded timing of formation and post-eruption tectonothermal event.Holistic lithogeochemistry and elements mapping of basaltic rocks were further reevaluated to provide insights into crustal contamination and formation of the ELIP.A zircon U–Pb age of 251.3±2.0 Ma of the Wude basalt recorded the youngest volcanic eruption event and was consistent with the age span of 251-263 Ma for the emplacement of the ELIP.Such zircons hadε_Hf(t)values ranging from7.3 to+2.2,identical to those of magmatic zircons from the intrusive rocks of the ELIP,suggesting that crust-mantle interaction occurred during magmatic emplacement,or crust-mantle mixing existed in the deep source region prior to deep melting.The apatite U–Pb age at 53.6±3.4 Ma recorded an early Eocene magmatic superimposition of a regional tectonothermal event,corresponding to the Indian–Eurasian plate collision.Negative Nb,Ta,Ti and P anomalies of the Emeishan basalt may reflect crustal contamination.The uneven Nb/La and Th/Ta values distribution throughout the ELIP supported a mantle plume model origin.Therefore,the ELIP was formed as a result of a mantle plume which was later superimposed by a regional tectonothermal event attributed to the Indian–Eurasian plate collision during early Eocene.     

Elemental and Sr–Nd isotopic geochemistry of Permian Emeishan flood basalts in Zhaotong,Yunnan Province,SW China

International Journal of Earth Sciences - This study presents new whole-rock elemental and isotopic data for the basalts from the Zhaotong area, located in the intermediate zone of the...     

A new metallogenic model of the Panzhihua giant V–Ti–iron oxide deposit (Emeishan Large Igneous Province) based on high-Mg olivine-bearing wehrlite and new field evidence

The Panzhihua layered intrusion hosts a giant V–Ti–iron oxide deposit with ore reserves estimated at 1333 Mt. Laser ablation inductively coupled plasma mass spectrometry (LA–ICP–MS) U–Pb zircon dating of comagmatic anorthosite yields a crystallization age of 259.77 ± 0.79 million years, coeval with the Emeishan flood basalts. Recently, we identified a small wehrlite dike in microgabbroic rocks and marbles. The wehrlite consists of high-Mg olivine phenocrysts with up to 90.44 wt.% Fo. Incompatible element-normalized patterns between bulk wehrlite and clinopyroxenes in gabbro suggest that they are cogenetic. The Panzhihua parental magma is estimated to have been picritic (～10 wt.% FeO and ～16 wt.% MgO), produced by partial fusion of garnet peridotite. Much of the melting occurred in garnet-facies mantle at an initial melting temperature of about 1530°C and pressure of ～3.4 GPa, suggesting involvement of a mantle plume. The degree of partial melting was rather modest and could have been generated by plume–lithosphere interaction or ascending plume-derived melting contaminated by lithospheric mantle. Field relationships show sharp contacts between the massive ores and gabbro, between wehrlite and fine-grained gabbro, and between disseminated ores and gabbro. Considering the entire intrusion, which is locally cut by dikes or veins of anorthosite, together with the occurrence of a breccia made up of gabbro clasts cemented by disseminated ores, we suggest that different types of magmas were generated by liquid differentiation in a deeper-level chamber. This differentiation could have resulted from double-diffusive convection cells, with melt later intruding into a higher-level chamber, rather than by crystal settling or in situ growth on the floor of the intrusion. However, rhythmic layering produced by in situ crystallization only occurs in the middle of the Panzhihua intrusion and was caused by periodic fluctuation in water pressure.     

U–Pb and Re–Os geochronology and geochemistry of the Donggebi Mo deposit,Eastern Tianshan,NW China: Insights into mineralization and tectonic setting

The Donggebi Mo deposit located in NW China is a newly discovered, large, stockwork-type Mo deposit with ore reserves of 441 Mt @ 0.115% Mo. Ore bodies occur along faults and fractures at the external contact zone of a concealed porphyritic granite and volcaniclastic rocks of Gandun Formation, spatially associated with a fine-grained granite. Mo-bearing veins are mainly assemblages of volatile-rich K-feldspar-quartz-oxide, K-feldspar-quartz, polymetallic sulfides and calcite-quartz. Zircon LA-ICP-MS U–Pb dating yielded concordant ages of 234.6 ± 2.7 Ma and 231.8 ± 2.4 Ma for the porphyritic granite and the fine-grained granite, respectively; molybdenite Re–Os dating gave an isochron age of 234.0 ± 2.0 Ma. These ages further confirm an important and extensive magmatic-metallogenic event in Eastern Tianshan during the Triassic Indosinian orogeny. Whole-rock major and trace element analyses indicate that the granitic rocks associated with Mo mineralization are high in Si, K, Rb, Th, Nb, Ta, Ga and LREE, but low in P, Ti, Sr and Ba, belonging to high-K calc-alkaline granites with A-type features. Magma was likely derived from the re-melting of thickened lower crust in a post-collision compression environment in the Late Permian, experienced strong crystal fractionation and formed the large Donggebi Mo deposit under an intra-plate extension setting in the Early to Middle Triassic.     

Anatomy of a large Ag–Pb–Zn deposit in the Great Xing'an Range,northeast China: metallogeny associated with Early Cretaceous magmatism

The Bairendaba vein-type Ag–Pb–Zn deposit, hosted in a Carboniferous quartz diorite, is one of the largest polymetallic deposits in the southern Great Xing'an Range. Reserves exceeding 8000 tonnes of Ag and 3 million tonnes of Pb?+?Zn with grades of 30 g/t and 4.5% have been estimated. We identify three distinct mineralization stages in this deposit: a barren pre-ore stage (stage 1), a main-ore stage with economic Ag–Pb–Zn mineralization (stage 2), and a post-ore stage with barren mineralization (stage 3). Stage 1 is characterized by abundant arsenopyrite?+?quartz and minor pyrite. Stage 2 is represented by abundant Fe–Zn–Pb–Ag sulphides and is further subdivided into three substages comprising the calcite–polymetallic sulphide stage (substage 1), the fluorite–polymetallic sulphide stage (substage 2), and the quartz–polymetallic sulphide stage (substage 3). Stage 3 involves an assemblage dominated by calcite with variable pyrite, galena, quartz, fluorite, illite, and chlorite. Fluid inclusion analysis and mineral thermometry indicate that the three stages of mineralization were formed at temperatures of 320–350°C, 200–340°C, and 180–240°C, respectively. Stage 1 early mineralization is characterized by low-salinity fluids (5.86–8.81 wt.% NaCl equiv.) with an isotopic signature of magmatic origin (δ¹⁸O_fluid = 10.45–10.65‰). The main ore minerals of stage 2 precipitated from aqueous–carbonic fluids (4.34–8.81 wt.% NaCl equiv.). The calculated and measured oxygen and hydrogen isotopic compositions of the ore-forming aqueous fluids (δ¹⁸O_fluid = 3.31–8.59‰, δD_fluid?=??132.00‰ to??104.00‰) indicate that they were derived from a magmatic source and mixed with meteoric water. Measured and calculated sulphur isotope compositions of hydrothermal fluids (δ³⁴S_∑S?=??1.2–3.8‰) indicate that the ore sulphur was derived mainly from a magmatic source. The calculated carbon isotope compositions of hydrothermal fluids (δ¹³C_fluid?=??26.52‰ to??25.82‰) suggest a possible contribution of carbon sourced from the basement gneisses. The stage 3 late mineralization is dominated (1.40–8.81 wt.% NaCl equiv.) by aqueous fluids. The fluids show lower δ¹⁸O_fluid (?16.06‰ to??0.70‰) and higher δD_fluid (?90.10‰ to??74.50‰) values, indicating a heated meteoric water signature. The calculated carbon isotope compositions (δ¹³C_fluid?=??12.82‰ to??6.62‰) of the hydrothermal fluids in stage 3 also suggest a possible contribution of gneiss-sourced carbon. The isotopic compositions and fluid chemistry indicate that the ore mineralization in the Bairendaba deposit was related to Early Cretaceous magmatism.