Origin of the Dexing Cu-bearing porphyries,SE China: elemental and Sr–Nd–Pb–Hf isotopic constraints

The Dexing porphyry copper deposit, part of the circum-Pacific porphyry copper ore belt, is the largest porphyry copper deposit in China. We present new LA–ICP–MS zircon U–Pb and molybdenite Re–Os dating, bulk-rock elemental and Sr–Nd–Pb isotopic as well as in situ zircon Hf isotopic geochemistry for these ore-bearing porphyries, in an attempt to better constrain their petrogenesis. LA–ICP–MS zircon U–Pb dating shows that the Dexing porphyries were emplaced in the early Middle Jurassic (～171 Ma); molybdenite Re–Os dating indicates that the associated Cu–Mo mineralization was contemporaneous (～171 Ma) with the igneous intrusion. The rocks are mainly high-K calc-alkaline and show adakitic affinities, including high Sr and low Y and Yb contents, high Sr/Y and La/Yb ratios, and high Mg# (higher than pure crustal melts). These porphyries have initial ⁸⁷Sr/⁸⁶Sr ratios of 0.7044?0.7047, ?_Nd(T) values of –1.5 to?+0.6, and ?_Hf(T) (in situ zircon) values of?+2.6 to?+4.6. They show unusually radiogenic Pb isotopic compositions with initial ²⁰⁶Pb/²⁰⁴Pb ratios up to 18.41 and ²⁰⁷Pb/²⁰⁴Pb up to 15.61. These isotopic compositions are distinctly different from either Pacific MORB or Yangtze lower crust but are similar to the subducting sediments in the western Pacific trenches. Detailed elemental and isotopic data suggest that the Dexing porphyries were emplaced in a continental arc setting coupled with westward subduction of the palaeo-Pacific plate. Partial melting involved the subducted slab (mainly the overlying sediments), with generated melts interacting with the lithospheric mantle wedge, thereby forming the investigated high-K calc-alkaline porphyry magmas.     

Geological and C–O–S–Pb–Sr isotopic constraints on the origin of the Qingshan carbonate-hosted Pb–Zn deposit,Southwest China

Located in the western Yangtze Block, the Qingshan Pb–Zn deposit, part of the Sichuan–Yunnan–Guizhou Pb–Zn metallogenic province, contains 0.3 million tonnes of 9.86 wt.% Pb and 22.27 wt.% Zn. Ore bodies are hosted in Carboniferous and Permian carbonate rocks, structurally controlled by the Weining–Shuicheng anticline and its intraformational faults. Ores composed of sphalerite, galena, pyrite, dolomite, and calcite occur as massive, brecciated, veinlets, and disseminations in dolomitic limestones.

The C–O isotope compositions of hydrothermal calcite and S–Pb–Sr isotope compositions of Qingshan sulphide minerals were analysed in order to trace the sources of reduced sulphur and metals for the Pb–Zn deposit. δ¹³C_PDB and δ¹⁸O_SMOW values of calcite range from –5.0‰ to –3.4‰ and +18.9‰ to +19.6‰, respectively, and fall in the field between mantle and marine carbonate rocks. They display a negative correlation, suggesting that CO₂ in the hydrothermal fluid had a mixed origin of mantle, marine carbonate rocks, and sedimentary organic matter. δ³⁴S values of sulphide minerals range from +10.7‰ to +19.6‰, similar to Devonian-to-Permian seawater sulphate (+20‰ to +35‰) and evaporite rocks (+23‰ to +28‰) in Carboniferous-to-Permian strata, suggesting that the reduced sulphur in hydrothermal fluids was derived from host-strata evaporites. Ores and sulphide minerals have homogeneous and low radiogenic Pb isotope compositions (²⁰⁶Pb/²⁰⁴Pb = 18.561 to 18.768, ²⁰⁷Pb/²⁰⁴Pb = 15.701 to 15.920, and ²⁰⁸Pb/²⁰⁴Pb = 38.831 to 39.641) that plot in the upper crust Pb evolution curve, and are similar to those of Devonian-to-Permian carbonate rocks. Pb isotope compositions suggest derivation of Pb metal from the host rocks. ⁸⁷Sr/⁸⁶Sr ratios of sphalerite range from 0.7107 to 0.7136 and (⁸⁷Sr/⁸⁶Sr)_200Ma ratios range from 0.7099 to 0.7126, higher than Sinian-to-Permian sedimentary rocks and Permian Emeishan flood basalts, but lower than Proterozoic basement rocks. This indicates that the ore strontium has a mixture source of the older basement rocks and the younger cover sequence. C–O–S–Pb–Sr isotope compositions of the Qingshan Pb–Zn deposit indicate a mixed origin of the ore-forming fluids and metals.     

Ore-forming material sources of the Jurassic Cu–Pb–Zn mineralization in the Qin–Hang ore belt,South China: Constraints from S–Pb isotopes

The Qin–Hang ore belt in South China, which serves as the boundary between the Yangtze and Cathaysia blocks, is marked by extensive Jurassic porphyry-skarn-metasomatic Cu–Pb–Zn polymetallic mineralization. In this contribution, S and Pb isotopic compositions of the Baoshan Cu–Pb–Zn deposit in the western portion of the Qin–Hang ore belt were analyzed to determine the ore-forming material sources in the area. This is coupled by the first systematic collection, compilation and interpretation of previously published S and Pb isotopic data of multiple sulfide minerals to reveal the metal origin and accumulation mechanism of the Cu–Pb–Zn mineralization from the significant deposits in the region (i.e., Dexing, Qibaoshan, Shuikoushan, Baoshan, Huangshaping, Tongshanling and Dabaoshan). The results show that Cu mineralization is characterized by low and narrow δ³⁴S (‰) range of values (–5 to 6) and Pb isotopic ratios (²⁰⁸Pb/²⁰⁴Pb = 38.0–39.0, ²⁰⁷Pb/²⁰⁴Pb = 15.4–15.8, and ²⁰⁶Pb/²⁰⁴Pb = 17.7–18.7), which are consistent with those of local porphyries. In contrast, the Pb–Zn mineralization reveals higher and more variable δ³⁴S (‰) values (–4 to 18) and Pb isotopic ratios (²⁰⁸Pb/²⁰⁴Pb = 38.0–39.5, ²⁰⁷Pb/²⁰⁴Pb = 15.3–16.0, and ²⁰⁶Pb/²⁰⁴Pb = 18.0–19.0) that correspond to wall-rock and basement rock compositions in the region. This indicates that the sulfur and lead that formed the Cu mineralization in the Qin–Hang ore belt was mainly sourced from regional magmatism with mantle contributions, whereas the sulfur and lead for the Pb–Zn mineralization was likely derived from the host sedimentary rocks and Proterozoic metamorphic basement rocks, respectively. The S and Pb isotopic data, combined with the geochemical signatures of mineralization-related porphyries, suggest that the Cu was sourced from the deeper levels along with mantle-derived magmas. In contrast, the Pb–Zn probably originated from the crust, with partial melting of the crystalline basement in the Cathaysia Block. Consequently, a three-stage genetic model is proposed to explain the ore-forming processes of the Qin–Hang Cu-polymetallic belt in South China.     

The Ordovician igneous rocks with high Sr/Y at the Tongshan porphyry copper deposit,satellite of the Duobaoshan deposit,and their metallogenic role

A strong link between high Sr/Y arc magmas and porphyry Cu–Mo–Au deposits has been recognized in recent years. The Tongshan and Duobaoshan deposits are representative large Cu–Mo–Au deposits in NE China. We report LA–ICP–MS zircon U–Pb crystallization age of 471.5 ± 1.3 Ma for Tongshan ore-related granitoid. Re–Os isotopic analyses of the two chalcopyrite samples from Tongshan deposit show a model age range of 470.2–477.1 Ma. The Duobaoshan and Tongshan ore-related granitoids show higher Sr/Y and La/Yb ratios. The δ³⁴S values of sulphides from the Duobaoshan and Tongshan deposits vary from −2.3‰ to 0.0‰, belonging to a magmatic-hydrothermal system. The Pb isotopic ratios of the sulphides from the Duobaoshan and Tongshan deposit range from 17.201 to 18.453 for ²⁰⁶Pb/²⁰⁴Pb, 15.445 to 15.551 for ²⁰⁷Pb/²⁰⁴Pb, and 36.974 to 37.999 for ²⁰⁸Pb/²⁰⁴Pb, indicating the addition of lower crustal material. The Duobaoshan and Tongshan granitoids were formed in a subduction-related continental arc setting, produced by partial melting of juvenile hydrous basalts underplating the deep continental crust during the Ordovician.     

Characteristics and genesis of Gangdese porphyry copper deposits in the southern Tibetan Plateau: Preliminary geochemical and geochronological results

Porphyry-type Cu (Mo, Au) deposits have been discovered along the Gangdese magmatic arc in the southern Tibetan Plateau. Extensive field investigations and systematic studies of geochemistry, S–Pb isotopic tracing, together with Re–Os and ⁴⁰Ar/³⁹Ar isotopic dating indicate that the mineralisation of the copper belt is genetically related to emplacement of late orogenic granitic porphyries during the post-collisional crustal relaxation period of the Late Himalayan epoch. These porphyries are petrochemically K-enriched and belong to shoshonitic to high-K calc-alkaline series. They display enrichment of large ion lithophile elements (LILE) Rb, K, U, Th, Sr, Pb and depletion of high field strength elements (HFSE) Nb, Ta, Ti and the heavy rare earth elements (HREE) and Y without Eu anomalies. These characteristics demonstrate that subduction played a dominant role in their petrogenesis and residual garnet was left in the magma sources. Pb isotope data show a linear correlation in the plumbotectonic framework diagram ranging from orogenic Pb in the eastern segment of the copper belt to mantle Pb in the western segment. These constitute a mixing line of the Indian Oceanic MORB with Indian Oceanic sediments and suggest that the porphyry magmas were dominantly derived from partial melting of subducted oceanic crusts mixed with a minor quantity of sediments and mantle wedge components.The Gangdese porphyry copper polymetallic belt has alteration characteristics and zonation typical of porphyry-type copper deposits which include potassic alteration (K-feldspathisation and biotitisation), silicification, sericitisation, and propylitisation. Mineralisation mainly occurs in strongly altered granitic cataclasite at the exo-contact with veinlet-disseminated textures. The porphyries themselves are weakly mineralised with disseminated pyrite and chalcopyrite. The copper deposits contain simple ore mineral associations consisting of chalcopyrite, pyrite, bornite, molybdenite, sphalerite and oxidised minerals of malachite, covellite and molybdite. During supergene oxidation, primary ores underwent secondary enrichment to form economic orebodies with Cu grade ranging from 1% to 5%.Ore sulphides of the copper belt display S and Pb isotopic compositions identical to the ore-bearing porphyries. Their δ³⁴S values vary between − 3.8‰ and + 2.4‰ and are typical of mantle sulphur. The ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb, and ²⁰⁸Pb/²⁰⁴Pb ratios vary in the ranges: 18.106 to 18.752, 15.501 to 15.638, and 37.394 to 39.058, respectively, and yielded radiogenetic lead-enriched signatures. Twelve molybdenite samples from the copper belt yielded isochron ages of 14.76 ± 0.22 Ma and 13.99 ± 0.16 Ma for the Nanmu and Chongjiang deposits and model ages of 13.5 to 13.6 Ma for the Lakang'e deposit. Meanwhile, ⁴⁰Ar/³⁹Ar isotopic dating of two biotite phenocrysts from the Chongjiang and Lakang'e deposits give plateau ages of 13.5 ± 1.0 Ma and 13.42 ±0.10 Ma, respectively. During the geodynamic evolution of the Gangdese collision-orogenic belt, intrusion of the ore-bearing porphyries took place just before the rapid uplift and E–W extension of the southern Plateau. And the ore-forming process may have occurred simultaneously with the uplift and extension (14 ± 0.1 Ma).     

Petrogenesis of Cretaceous igneous rocks from the Duolong porphyry Cu–Au deposit,central Tibet: evidence from zircon U–Pb geochronology,petrochemistry and Sr–Nd–Pb–Hf isotope characteristics

The Duolong porphyry Cu–Au deposit (5.4 Mt at 0.72% Cu, 41 t at 0.23 g/t Au) was recently discovered in the southern Qiangtang terrane, central Tibet. Here, new whole‐rock elemental and Sr–Nd–Pb isotope and zircon Hf isotopic data of syn‐ and post‐ore volcanic rocks and barren and ore‐bearing granodiorite porphyries are presented for a reconstruction of magmas associated with Cu–Au mineralization. LA–ICP–MS zircon U–Pb dating yields mean ages of 117.0 ± 2.0 and 120.9 ± 1.7 Ma for ore‐bearing granodiorite porphyry and 105.2 ± 1.3 Ma for post‐ore basaltic andesite. All the samples show high‐K calc‐alkaline compositions, with enrichment of light rare earth elements (LREE) and large ion lithophile elements (LILE: Cs and Rb) and depletion of high field strength elements (HFSE: Nb and Ti), consistent with the geochemical characteristics of arc‐type magmas. Syn‐ and post‐ore volcanic rocks show initial Sr ratios of 0.7045–0.7055, ε_Nd(t) values of −0.8 to 3.6, (²⁰⁶Pb/²⁰⁴Pb)_t ratios of 18.408–18.642, (²⁰⁷Pb/²⁰⁴Pb)_t of 15.584–15.672 and positive zircon ε_Hf(t) values of 1.3–10.5, likely suggesting they dominantly were derived from metasomatized mantle wedge and contaminated by southern Qiangtang crust. Compared to mafic volcanic rocks, barren and ore‐bearing granodiorite porphyries have relatively high initial Sr isotopic ratios (0.7054–0.7072), low ε_Nd(t) values (−1.7 to −4.0), similar Pb and enriched zircon Hf isotopic compositions [ε_Hf(t) of 1.5–9.7], possibly suggesting more contribution from southern Qiangtang crust. Duolong volcanic rocks and granodiorite porphyries likely formed in a continental arc setting during northward subduction of the Bangong–Nujiang ocean and evolved at the base of the lower crust by MASH (melting, assimilation, storage and homogenization) processes. Copyright © 2014 John Wiley & Sons, Ltd.     

Petrogenesis of Quebrada de la Mina and Altar North porphyries (Cordillera of San Juan,Argentina): Crustal assimilation and metallogenic implications

We investigate the geology of Altar North (Cu–Au) and Quebrada de la Mina (Au) porphyry deposits located in San Juan Province (Argentina), close to the large Altar porphyry copper deposit (995 Mt, 0.35% Cu, 0.083 g/t Au), to present constraints on the magmatic processes that occurred in the parental magma chambers of these magmatic-hydrothermal systems. Altar North deposit comprises a plagioclase-amphibole-phyric dacite intrusion (Altar North barren porphyry) and a plagioclase-amphibole-biotite-phyric dacite stock (Altar North mineralized porphyry, 11.98 ± 0.19 Ma). In Quebrada de la Mina, a plagioclase-amphibole-biotite-quartz-phyric dacite stock (QDM porphyry, 11.91 ± 0.33 Ma) crops out. High Sr/Y ratios (92–142) and amphibole compositions of Altar North barren and QDM porphyries reflect high magmatic oxidation states (fO₂ = NNO +1.1 to +1.6) and high fH₂O conditions in their magmas. Zones and rims enriched in anorthite (An_37–48), SrO (0.22–0.33 wt.%) and FeO (0.21–0.37 wt.%) in plagioclase phenocrysts are evidences of magmatic recharge processes in the magma chambers. Altar North and Quebrada de la Mina intrusions have relatively homogeneous isotopic compositions (⁸⁷Sr/⁸⁶Sr_(t) = 0.70450–0.70466, ε_Nd(t) = +0.2 to +1.2) consistent with mixed mantle and crust contributions in their magmas. Higher Pb isotopes ratios (²⁰⁷Pb/²⁰⁴Pb = 15.6276–15.6294) of these intrusions compared to other porphyries of the district, reflect an increase in the assimilation of high radiogenic Pb components in the magmas. Ages of zircon xenocrysts (297, 210, 204, 69 Ma) revealed that the magmas have experienced assimilation of Miocene, Cretaceous, Triassic and Carboniferous crustal rocks.Fluids that precipitated sulfides in the Altar deposit may have remobilized Pb from the host rocks, as indicated by the ore minerals being more radiogenic (²⁰⁷Pb/²⁰⁴Pb = 15.6243–15.6269) than their host intrusions. Au/Cu ratio in Altar porphyries (average Au/Cu ratio of 0.14 × 10^?4 by weight in Altar Central) is higher than in the giant Miocene porphyry deposits located to the south: Los Pelambres, Río Blanco and Los Bronces (Chile) and Pachón (Argentina). We suggest that the increase in Au content in the porphyries of this region could be linked to the assimilation of high radiogenic Pb components in the magmas within these long-lived maturation systems.     

Genesis of the giant Zijinshan epithermal Cu-Au and Luoboling porphyry Cu–Mo deposits in the Zijinshan ore district,Fujian Province,SE China: A multi-isotope and trace element investigation

The Zijinshan ore district occurs as one of the largest porphyry-epithermal Cu–Au–Mo ore systems in South China, including the giant Zijinshan epithermal Cu–Au deposit and the large Luoboling porphyry Cu–Mo deposit. The mineralization is intimately related to Late Mesozoic large-scale tectono-magmatic and hydrothermal events. The Cu–Au–Mo mineralization occurs around intermediate-felsic volcanic rocks and hypabyssal porphyry intrusions. In this study, we summarize previously available Re–Os isotopes, zircon U–Pb age and trace elements, and Sr–Nd–Pb isotope data, and present new Pb–S and Re–Os isotope data and zircon trace elements data for ore-related granitoids from the Zijinshan high-sulfidation epithermal Cu–Au deposit and the Luoboling porphyry Cu–Mo deposit, in an attempt to explore the relationship between the two ore systems for a better understanding of their geneses. The ore-bearing porphyritic dacite from the Zijinshan deposit shows a zircon U-Pb age of 108–106 Ma and has higher zircon Ce⁴⁺/Ce³⁺ ratios (92–1568, average 609) but lower Ti-in-zircon temperatures (588–753 °C, average 666 °C) when compared with the barren intrusions in the Zijinshan ore district. Relative to the Zijinshan porphyritic dacite, the ore-bearing granodiorite porphyry from the Luoboling deposit show a slightly younger zircon U–Pb age of 103 Ma, but has similar or even higher zircon Ce⁴⁺/Ce³⁺ ratios (213–2621, average 786) and similar Ti-in-zircon temperatures (595–752 °C, average 675 °C). These data suggest that the ore-bearing magmatic rocks crystallized from relatively oxidized and hydrous magmas. Combined with the high rhenium contents (78.6–451 ppm) of molybdenites, the Pb and S isotopic compositions of magmatic feldspars and sulfides suggest that the porphyry and ore-forming materials in the Luoboling Cu–Mo deposit mainly originated from an enriched mantle source. In contrast, the ore-bearing porphyritic dacite in the Zijinshan Cu–Au deposit might be derived from crustal materials mixing with the Cathaysia enriched mantle. The fact that the Zijinshan Cu–Au deposit and the Luoboling Cu–Mo deposit show different origin of ore-forming materials and slightly different metallogenic timing indicates that these two deposits may have been formed from two separate magmatic-hydrothermal systems. Crustal materials might provide the dominant Cu and Au in the Zijinshan epithermal deposit. Cu and Au show vertical zoning and different fertility because the gold transports at low oxygen fugacity and precipitates during the decreasing of temperature, pressure and changing of pH conditions. It is suggested that there is a large Cu–Mo potential for the deeper part of the Zijinshan epithermal Cu–Au deposit, where further deep drilling and exploration are encouraged.     

Geology and Lead–Sulphur Isotope Compositions of the Tongyu Volcanic-Hosted Massive Sulphide Copper Deposit in the Western Part of the North Qinling Orogen, China

The Tongyu copper deposit, located in the western part of the North Qinling Orogen, China, is one of several volcanic-hosted massive sulphide(VHMS) deposits with industrial value and is also a typical example of mineralization related to the subduction and metallogenesis during the Caledonian orogeny. We conducted systematic lead-sulphur isotope geochemical analyses of the Tongyu deposit to understand the possible ore-forming material sources and tectonic settings. Twenty-six sulphide samples yielded clustered δ~(34)S_(CDT) values of 1.13‰-3.36‰, average 2.22‰, and show a tower-type distribution,implying that the sulphur of the Tongyu copper deposit mainly originated from a mantle source. The Pb isotope compositions of sulphides(~(206)Pb/~(204)Pb = 17.59225-18.56354, average 18.32020; ~(207)Pb/~(204)Pb =15.51770-15.69381, average 15.66217; ~(208)Pb/~(204)Pb= 37.99969-39.06953, average 38.52722) are close to the values of the volcanic host rocks(~(206)Pb/~(204)Pb= 18.10678-18.26293, average 18.21158; ~(207)Pb/~(204)Pb =15.63196-15.68188, average 15.65345; ~(208)Pb/~(204)Pb= 38.43676-38.56360, average 38.49171), thus consistent with the Pb in ores and volcanic host rocks having been derived from a common source that was island-arc Pb related to oceanic crust subduction. The northward subduction of the Palaeo-Qinling oceanic crust triggered dehydration of the slab, which generated a large amount of high-oxygen-fugacity aqueous hydrothermal fluid. The fluid rose into the mantle wedge, activated and extracted metallogenic material and promoted partial melting of the mantle wedge. The magma and ore-forming fluid welled up and precipitated, finally forming the Tongyu VHMS copper deposit.     

Chalcophile elemental compositions and origin of the Tuwu porphyry Cu deposit,NW China

The Tuwu porphyry Cu deposit in the eastern Tianshan Orogenic Belt of southern Central Oceanic Orogen Belt contains 557 Mt ores at an average grade of 0.58 wt.% Cu and 0.2 g/t Au, being the largest porphyry Cu deposit in NW China. The deposit is genetically related to dioritic and plagiogranitic porphyries that intruded the Carboniferous Qieshan Group. Ore minerals are dominantly chalcopyrite, pyrite and enargite. Porphyric diorites have Sr/Y and La/Yb_N ratios lower but Y and Yb contents higher than plagiogranites. Diorites have highly variable Cu but nearly constant PGE contents (most Pd = 0.50–1.98 ppb) with Cu/Pd ratios ranging from 10,900 to 8,900,000. Plagiogranites have PGEs that are positively correlated with Cu and have nearly uniform Cu/Pd ratios (5,100,000 to 7,800,000). Diorites have concentrations of Re (0.73–15.18 ppb), and ¹⁸⁷Re/¹⁸⁸Os and ¹⁸⁷Os/¹⁸⁸Os ratios lower but common Os contents (0.006–0.097 ppb) higher than plagiogranites. However, both the diorites and plagiogranites have similar normalized patterns of rare earth elements (REE), trace element and platinum-group elements (PGEs). All the samples are characterized by the enrichments of LREE relative to HREE and display positive anomalies of Pb and Sr but negative anomalies of Nb and Ta in primitive-mantle normalized patterns. In the primitive mantle-normalized siderophile element diagrams, they are similarly depleted in all PGEs but slightly enriched in Au relative to Cu.Our new dataset suggests that both the diorite and plagiogranite porphyries were likely evolved from magmas derived from partial melting of a wet mantle wedge. Their parental magmas may have had different water contents and redox states, possibly due to different retaining time in staging magma chambers at the depth, and thus different histories of magma differentiation. Parental magmas of the diorite porphyries are relatively reduced with less water contents so that they have experienced sulfide saturation before fractional crystallization of silicate minerals, whereas the relatively more oxidized parental magmas with higher water contents of the plagiogranite porphyries did not reach sulfide saturation until the magmatic-hydrothermal stage. Our PGE data also indicates that the Cu mineralization in the Tuwu deposit involved an early stage with the enrichments of Au, Mo and Re and a late stage with the enrichment of As but depletion of Au–Mo. After the formation of the Cu mineralization, meteoric water heated by magmas penetrated into and interacted with porphyritic rocks at Tuwu, which was responsible for leaching Re from hosting rocks.     

Evolution of magmatic-hydrothermal system of the Kalaxiange’er porphyry copper belt and implications for ore formation (Xinjiang,China)

The Kalaxiange’er porphyry copper ore belt is situated in the eastern part of the southern Altai of the Central Asian Orogenic Belt and forms part of a broad zone of Cu porphyry mineralization in southern Mongolia, which includes the Oyu Tolgoi ore district and other copper–gold deposits. The copper ore bodies are spatially associated with porphyry intrusions of granodiorite, quartz diorite, quartz syenite, and quartz monzonite and have a polygenetic (polychromous) origin (magmatic porphyry, hydrothermal, and supergene). The mineralized porphyries are characterized by almost identical REE and trace element patterns. The Zr/Hf and Nb/Ta ratios are similar to those of normal granite produced through the evolution of mantle magma. The low initial Sr isotope ratio I_Sr, varying within a narrow range of values (0.703790–0.704218), corresponds to that of primitive mantle, whereas the εNd(T) value of porphyry varies from 5.8 to 8.4 and is similar to that of MORB. These data testify to the upper-mantle genesis of the parental magmas of ore-bearing porphyry, which were then contaminated with crustal material in an island-arc environment. The isotopic composition of sulfur (unimodal distribution of δ34S with peak values of − 2 to − 4‰) evidences its deep magmatic origin; the few lower negative δ³⁴S values suggest that part of S was extracted from volcanic deposits later. The isotopic characteristics of Pb testify to its mixed crust–upper-mantle origin. According to SHRIMP U–Pb geochronological data for zircon from granite porphyry and granodiorite porphyry, mineralization at the Xiletekehalasu porphyry Cu deposit formed in two stages: (1) Hercynian “porphyry” stage (375.2 ± 8.7 Ma), expressed as the formation of porphyry with disseminated and vein–disseminated mineralization, and (2) Indosinian stage (217.9 ± 4.2 Ma), expressed as superposed hydrothermal mineralization. The Re–Os isotope data on molybdenite (376.9 ± 2.2 Ma) are the most consistent with the age of primary mineralization at the Xiletekehalasu porphyry Cu deposit, whereas the Ar–Ar isotopic age (230 ± 5 Ma) of K-feldspar–quartz vein corresponds to the stage of hydrothermal mineralization. The results show that mineralization at the Xiletekehalasu porphyry Cu deposit was a multistage process which resulted in the superposition of the Indosinian hydrothermal mineralization on the Hercynian porphyry Cu mineralization.     

Early Cretaceous A-type granites and Mo mineralization,Aershan area,eastern Inner Mongolia,Northeast China: geochemical and isotopic constraints

The Jiazishan porphyry-type molybdenum deposit is located in the eastern Inner Mongolia Autonomous Region in China. Mineralization occurs mainly as veins, lenses, and layers within the host porphyry. To better understand the link between mineralization and host igneous rocks, we studied samples from underground workings and report new SHRIMP II zircon U–Pb and Re–Os molybdenite ages, and geochemical data from both the molybdenites and the porphyry granites. Seven molybdenite samples yield a Re–Os isochron weighted mean age of 135.4 ± 2.1 Ma, whereas the porphyry granite samples yield crystallization ages of 139 ± 1.5 Ma (Jiazishan deposit) and 133 ± 1 Ma (Taolaituo deposit). The U–Pb and Re–Os ages are similar, suggesting that the mineralization is genetically related to Early Cretaceous porphyry emplacement. Re contents of the molybdenite range from 21.74 ppm to 52.08 ppm, with an average of 35.92 ppm, whereas δ³⁴ S values of the sulphide vary from 1.3‰ to 4.2‰. The ores have ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb, and ²⁰⁸Pb/²⁰⁴Pb ratios of 18.178–18.385, 15.503–15.613, and 37.979–38.382, respectively. We also obtained a weighted mean U–Pb zircon age of 294.2 ± 2.1 Ma for the oldest granite in Jiazishan area. All granites are A-type granites. These observations indicate that the molybdenites and the porphyry granites were derived from a mixed source involving young accretionary materials and enriched subcontinental lithospheric mantle. A synthesis of geochronological and geological data reveals that porphyry emplacement and Mo mineralization in the Jiazishan deposit occurred contemporaneously with Early Cretaceous tectonothermal events associated with lithospheric thinning, which was caused by delamination and subsequent upwelling of the asthenosphere associated with intra-continental extension in Northeast China.     

Geology,geochronology and geochemistry of granitic intrusions and the related ores at the Hongshan Cu-polymetallic deposit: Insights into the Late Cretaceous post-collisional porphyry-related mineralization systems in the southern Yidun arc,SW China

The Hongshan Cu-polymetallic deposit is located in the southern Yidun arc in southwestern China, where both subduction-related (Late Triassic) and post-collisional (Late Cretaceous) porphyry–skarn–epithermal mineralization systems have been previously recognized. In this study, two distinct magmatic events, represented by diorite porphyry and quartz monzonite porphyry, have been revealed in the Hongshan deposit, with zircon SHRIMP U–Pb ages of 214 ± 2 Ma and 73.4 ± 0.7 Ma, respectively. The 73 Ma age is comparable to the Re–Os ages of 77 to 80 Ma of ore minerals from the Hongshan deposit, indicating that the mineralization is related to the Late Cretaceous quartz monzonite porphyries rather than Late Triassic diorite porphyries. The Late Triassic diorite porphyries belong to the high-K calc-alkaline series and show arc magmatic geochemical characteristics such as enrichment in Rb, Ba, Th and U and depletion in HFSEs, indicating that they were formed during the westward subduction of the Garzê–Litang Ocean. In contrast, the Late Cretaceous quartz monzonite porphyries show shoshonitic I-type geochemical characteristics, with high SiO₂, K₂O, LILE, low HREE, Y and Yb contents, and high LREE/HREE and La/Yb ratios. These geochemical characteristics, together with the Sr–Nd–Pb isotopic compositions (average (⁸⁷Sr/⁸⁶Sr)_i = 0.7085; ε_Nd(t) = − 6.0; ²⁰⁶Pb/²⁰⁴Pb = 19.064, ²⁰⁷Pb/²⁰⁴Pb = 15.738, ²⁰⁸Pb/²⁰⁴Pb = 39.733) suggest that the quartz monzonite porphyries originated from the partial melting of the ancient lower crust in response to underplating of mafic magma from subduction metasomatized mantle lithosphere, possibly triggered by regional extension in the post-collisional tectonic stage. The S isotopic compositions (δ³⁴S_V-CDT = 3.81‰ to 5.80‰) and Pb isotopic compositions (²⁰⁶Pb/²⁰⁴Pb = 18.014 to 18.809, ²⁰⁷Pb/²⁰⁴Pb = 15.550 to 15.785, and ²⁰⁸Pb/²⁰⁴Pb = 38.057 to 39.468) of ore sulfides indicate that the sulfur and metals were derived from mixed mantle and crustal sources. It is proposed that although the Late Triassic magmatic event is not directly related to mineralization, it contributed to the Late Cretaceous mineralization system through the storage of large amounts of sulfur and metals as well as water in the cumulate zone in the mantle lithosphere through subduction metasomatism. Re-melting of the mantle lithosphere including the hydrous cumulate zone and ancient lower crust during the post-collisional stage produced fertile magmas, which ascended to shallow depths to form quartz monzonite porphyries. Hydrothermal fluids released from the intrusions resulted in porphyry-type Mo–Cu ores in and near the intrusions, skarn-type Cu–Mo ores in the country rocks above the intrusions, and hydrothermal Pb–Zn ores in the periphery.     

A reappraisal of the evolution of the palaeo-Pacific margin of Gondwana from the Pb and Os isotope systematics of igneous rocks from the southern Adelaide fold belt,South Australia

We have undertaken Pb and Os isotopic analyses of igneous rocks from the southern Adelaide fold belt to further understanding of the Neoproterozoic – early Palaeozoic evolution of the palaeo-Pacific margin of Gondwana. The new Pb isotope data and a reappraisal of existing geochronological data suggest that layered mafic intrusions at Black Hill and Cambrai may have intruded much earlier than previously thought. Intrusion may even have occurred prior to deposition of the Normanville and Kanmantoo Group sediments and the onset of what is traditionally regarded as the Delamerian Orogeny. We tentatively term this earlier event the Hallett Cove orogeny. However, equivalent ages are common in the formerly adjacent Ross Orogen. When the Pb isotope signatures of the suites of gabbros, and I-, S-, and A-type granites are compared at 487 Ma they all span a very large range (²⁰⁶Pb/²⁰⁴Pb_i = 15.4–18.7, ²⁰⁷Pb/²⁰⁴Pb_i = 15.4–15.7, ²⁰⁸Pb/²⁰⁴Pb_i = 33.0–38.8) compared with other formerly adjacent terranes or the subsequent Lachlan fold belt. Similarly, ¹⁸⁷Os/¹⁸⁸Os_i ratios span 0.122–1.17 but include one gabbro and one rhyolite that have subchondritic ¹⁸⁷Os/¹⁸⁸Os_i ratios. When taken together, the combined data do not support models in which the observed range in initial isotope ratios reflects major and variable mid to upper crustal assimilation of magmas derived from the contemporary asthenospheric mantle. Rather, it appears that magmas parental to the gabbros and A-type rocks were derived from subduction-modified lithospheric mantle that has a median metasomatic age of 1.4 Ga. Large-scale Pb isotopic homogenization, as proposed for the Lachlan fold belt did not occur in the Adelaide fold belt.     

Ore genesis of the Tianbaoshan carbonate-hosted Pb–Zn deposit,Southwest China: geologic and isotopic (C–H–O–S–Pb) evidence

The Tianbaoshan Pb–Zn deposit, part of the Sichuan–Yunnan–Guizhou (SYG) Pb–Zn metallogenic province, is located in the western Yangtze Block and contains 2.6 million tonnes of 10–15 wt.% Pb + Zn metals. Ore bodies occur as vein or tubular types and are hosted in Sinian (late Proterozoic) carbonate rocks and are structurally controlled by the SN-trending Anninghe tectonic belt and NW-trending concealed fractures. The deposits are simple in mineralogy, with sphalerite, galena, pyrite, chalcopyrite, arsenopyrite, freibergite, and pyrargyrite as ore minerals and dolomite, calcite, and quartz as gangue minerals. These phases occur as massive, brecciated, veinlet, and dissemination in dolostone of the upper Sinian Dengying Formation. Hydrogen and oxygen isotope compositions of hydrothermal fluids range from –47.6 to –51.2‰ and –1.7 to +3.7‰, respectively. These data suggest that H₂O in hydrothermal fluids had a mixed origin of metamorphic and meteoric waters. Carbon and oxygen isotope compositions range from –6.5 to –4.9‰ and +19.3 to +20.2‰, respectively. These compositions plot in the field between mantle and marine carbonate rocks with a negative correlation, suggesting that CO₂ in the ore-forming fluids had multiple sources, including the Permian Emeishan flood basalts, Sinian-to-Permian marine carbonate rocks, and organic matters in Cambrian-to-Permian sedimentary rocks. Sulphur isotope compositions range from –0.4 to +9.6‰, significantly lower than Cambrian-to-Permian seawater sulphate (+15 to +35‰) and sulphate (+15 to +28‰) from evaporates in Cambrian-to-Permian strata, implicating that the S was derived from host-strata evaporates by thermal–chemical sulphate reduction. ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb, and ²⁰⁸Pb/²⁰⁴Pb ratios range from 18.110 to 18.596, 15.514 to 15.878, and 38.032 to 39.221, respectively, which plot in field of the upper crust Pb evolution curve, unlike those of Proterozoic basement rocks, Sinian dolostone, Devonian-to-Permian carbonate rocks, and the Permian Emeishan flood basalts, implying complex derivation of Pb metal in the ore-forming fluids. Geological and isotopic studies of the Tianbaoshan Pb–Zn deposit reveal that constituents in the hydrothermal fluids were derived from multiple sources and that fluid mixing was a possible metallogenic mechanism. The studied deposit is not distal magmatic–hydrothermal, sedimentary exhalative (SEDEX), or Mississippi Valley (MVT) types, rather, it represents a unique ore deposit type, named in this article the SYG type.     

Crustal contamination and mantle source characteristics in continental intra-plate volcanic rocks: Pb, Hf and Os isotopes from central European volcanic province basalts

We report new Os-Pb-Hf isotope data for a suite of alkaline to basaltic (nephelinites, basanites, olivine tholeiites to quartz-tholeiites) lavas from the Miocene Vogelsberg (Germany), the largest of the rift-related continental volcanic complexes of the Central European Volcanic Province (CEVP). ¹⁸⁷Os/¹⁸⁸Os in primitive (high-MgO) alkaline lavas show a much wider range than has been observed in alkaline basalts and peridotite xenoliths from elsewhere in the CEVP, from ratios similar to those in modern MORB and OIB (0.1260-0.1451; 58.9-168 ppt Os) to more radiogenic ratios (0.1908 and 0.2197; 27.6-15.1 ppt Os). Radiogenic Os is associated with high ε_Hf and ε_Nd, low ⁸⁷Sr/⁸⁶Sr and does not correlate with Mg^∗ or incompatible trace elements (e.g. Ce/Pb), suggesting the presence of a radiogenic endmember in the mantle rather than crustal contamination as the source of radiogenic Os. This contrasts with another high-Mg alkaline lava characterized by highly radiogenic ¹⁸⁷Os/¹⁸⁸Os (0.4344, 10.3 ppt Os), lower ε_Hf and ε_Nd, higher ⁸⁷Sr/⁸⁶Sr, and Pb isotope signatures than the other alkaline lavas with similar trace element composition suggestive of contamination with crustal material. Hafnium (ε_Hf: +8.9 to +5.0) and Pb isotope compositions (²⁰⁶Pb/²⁰⁴Pb: 19.10-19.61; ²⁰⁷Pb/²⁰⁴Pb: 15.56-15.60) of the alkaline rocks fall within the range of enriched MORB and some OIB. The Vogelsberg tholeiites show even more diverse ¹⁸⁷Os/¹⁸⁸Os, ranging from 0.1487 in Os-rich olivine tholeiite (31.7 ppt) to ratios as high as 0.7526 in other olivine-tholeiites and in quartz-tholeiites with lower Os concentrations (10.3-2.0 ppt). Low-¹⁸⁷Os/¹⁸⁸Os tholeiites show Pb-Hf isotope ratios (²⁰⁶Pb/²⁰⁴Pb:18.81; ²⁰⁷Pb/²⁰⁴Pb: 15.61; ε_Hf: +2.7) that are distinct from those in alkaline lavas with similar ¹⁸⁷Os/¹⁸⁸Os and originate from a different mantle source. By contrast, the combination of radiogenic Os and low ²⁰⁶Pb/²⁰⁴Pb and ε_Hf in the other tholeiites probably reflects crustal contamination.The association at Vogelsberg of primitive alkaline and tholeiitic lavas with a range of MORB- to OIB-like Os-Pb-Hf-Nd-Sr isotopic characteristics requires at least two asthenospheric magma sources. This is consistent with trace element modelling which suggests that the alkaline and tholeiitic parent magmas represent mixtures of melts from garnet and spinel peridotite sources (both with amphibole), implying an origin of the magmas in the garnet peridotite-spinel peridotite transition zone, probably at the asthenosphere-lithosphere interface. We propose that uncontaminated Vogelsberg lavas originated in ‘metasomatized’ mantle, involving a 3-stage model: (1) early carbonatite metasomatism several 10-100 Ma before the melting event (2) deposition of low-degree asthenospheric melts from carbonated peridotite at the lithosphere-asthenosphere thermal boundary produces hydrous amphibole-bearing veins or patches, and (3) remobilization of this modified lithospheric mantle into other asthenospheric melts passing through the same area later. In keeping with ‘metasomatized’ mantle models for other continental basalt provinces, we envisage that stage (2) is short-lived (few Ma), thus producing a prominent lithospheric trace element signature without changing the asthenospheric isotopic signatures. Models of this type can explain the peculiar mix of lithospheric (prominent depletions of Rb and K) and asthenospheric (OIB-like high ¹⁸⁷Os/¹⁸⁸Os, ¹⁴³Nd/¹⁴⁴Nd and ¹⁷⁶Hf/¹⁷⁷Hf) signatures observed in the Vogelsberg and many other continental basalt suites.     

http://www.sciencedirect.com/science/article/pii/S1674987113000790

The Heilangou gold deposit is located in the northern QixiaePenglai gold belt, which is one amongst the three large gold belts in the eastern Shandong Province （Jiaodong Peninsula）. The ore body has formed within the Guojialing granite. In this study, we report the mineral chemistry of pyrite, as well as the S, Pb, and HeO isotope data of the Heilangou gold deposit. The chemical composition of pyrite in the Heilangou gold deposit indicates that the associated gold deposit is a typical magmatic hydrothermal one. The geochemical signatures and crystal structure of pyrite show that the ore-forming materials have been derived from the crust. The S isotope data of the pyrites from Heilangou show an overall range from 5.5 to 7.8＆amp;and an average of 6.7＆amp;. The S isotope data in this deposit are similar to those from the deposits in the Jiaodong gold belt. The Pb and S isotope variations are small in the Heilangou gold deposit. The 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb ratios are 17.4653e17.5958, 15.5105e15.5746 and 38.0749e38.4361, respec-tively. These data plot between the lower crust and the orogenic belt. The Pb isotope data in the Heilangou gold deposit are similar to those in the Linglong gold deposit. From the Qixia gold area （the Liukou and Majiayao gold deposits） to the MupingeRushan gold belt （Rushan gold deposit） to the ZhaoeYe gold belt （the Linglong, Sanshandao and Jiaojia gold deposits）, the 206Pb/204Pb ratios progressively increase. The DeO isotope data obtained from quartz separates suggest that the ore-forming fluid was similar to a mixture of magmatic and meteoric waters. These results suggest that the ore-forming elements were primarily from source fluids derived from the lower crust.     

Sources of primitive alkaline volcanic rocks from the Central European Volcanic Province (Rhön,Germany) inferred from Hf,Os and Pb isotopes

Basanites and nephelinites from the Tertiary Rhön area (Germany), which are part of the Central European Volcanic Province (CEVP), have high MgO, Ni and Cr contents and prominent garnet signatures indicating that they represent near-primary magmas formed by melting of a CO₂-bearing peridotitic mantle source at high pressure. The Pb and Hf isotope (and previously published Nd and Sr isotope) ratios of the Rhön lavas are rather uniform, whereas the Os isotope composition is highly variable. For the most primitive basanites, Pb, Os and Hf isotope compositions fall within the range of enriched MORB and some OIB. Other basanites and nephelinites with low Os concentrations have distinctly more radiogenic Os (¹⁸⁷Os/¹⁸⁸Os: 0.160–0.469) isotope compositions, which are inferred to originate from crustal contamination. The samples with the highest Os concentrations have the lowest Os isotope ratios (¹⁸⁷Os/¹⁸⁸Os_(23 Ma): 0.132–0.135), and likely remain unaffected by crustal contamination. Together with their fairly depleted Sr, Nd and Hf isotope ratios, the isotopic composition of the Rhön lavas suggests derivation from an asthenospheric mantle source. Prominent negative K and Rb anomalies, however, argue for melting amphibole or phlogopite-bearing sources, which can only be stable in the cold lithosphere. We therefore propose that asthenospheric melts precipitated at the asthenosphere-lithosphere thermal boundary as veins in the lithospheric mantle and were remelted or incorporated after only short storage times (about 10–100 million years) by ascending asthenospheric melts. Due to the short residence time incorporation of the vein material imposes the prominent phlogopite/amphibole signature of the Rhön alkaline basalts but does not lead to a shift in the isotopic signatures. Melting of the lithospheric mantle cannot strictly be excluded, but has to be subordinate due to the lack of the respective isotope signatures, in good agreement with the fairly thin lithosphere observed in the Rhön area. The fairly radiogenic Pb isotope signatures are expected to originate from melting of enriched, low melting temperature portions incorporated in the depleted upper (asthenospheric) mantle and therefore do not require upwelling of deep-seated mantle sources for the Rhön or many other continental alkaline lavas with similar Pb isotope signatures.     

The genetic relationship between Habo alkaline intrusion and its surrounding deposits,Yunnan Province,China: geological and S–Pb isotopic evidences

The Habo alkaline intrusion, which is located in the south of the Sanjiang area, Yunnan Province, China, is a typical Cenozoic alkaline intrusion. There are a series of small to medium-sized Au and Pb–(Zn) deposits around this intrusion. Those deposits are spatially associated with the Habo alkaline intrusion. (1) The δ³⁴S values of sulfides from Au deposits range from ?1.91 ‰ to 2.69 ‰, which are similar to those of Pb–(Zn) deposits (?3.82 ‰ to ?0.05 ‰) and both indicate a much greater contribution from magma. (2) The Habo alkaline intrusion has relatively homogeneous Pb isotopic compositions with ²⁰⁶Pb/²⁰⁴Pb ranging from 18.608 to 18.761, ²⁰⁷Pb/²⁰⁴Pb from 15.572 to 15.722 and ²⁰⁸Pb/²⁰⁴Pb from 38.599 to 39.110. These Pb isotope ratios are similar to those of Au deposits, whose ²⁰⁶Pb/²⁰⁴Pb range from 18.564 to 18.734, ²⁰⁷Pb/²⁰⁴Pb from 15.582 to 15.738 and ²⁰⁸Pb/²⁰⁴Pb from 38.592 to 39.319. Pb ratios in both the intrusion and Au deposits suggest that Pb mainly derived from the depth, probably represents a mixture of mantle and crust. Pb–(Zn) deposits, however, show a decentralized trait, and most of them are similar to that of the alkaline intrusion with ²⁰⁶Pb/²⁰⁴Pb ranging from 18.523 to 18.648, ²⁰⁷Pb/²⁰⁴Pb from 15.599 to 15.802, and ²⁰⁸Pb/²⁰⁴Pb from 38.659 to 39.206. (3) In the plumbotectonic diagram ²⁰⁷Pb/²⁰⁴Pb versus ²⁰⁶Pb/²⁰⁴Pb, almost all of Au and Pb–(Zn) deposits have the same projection area with the Habo alkaline intrusion, which indicates that those deposits almost share the same source with the alkaline intrusion. (4) Isotopic age of the Habo alkaline intrusion is 36–33 Ma, which is similar to that of Beiya, whose ore-related alkaline porphyries age is 38–31 Ma and molybdenite Re–Os age is 36.9 Ma. Therefore, along with S–Pb isotope traits, we suggest that the Habo Au and Pb–(Zn) deposits should be typically Ailaoshan-Red RiverCenozoicalkaline-related deposits and ore-forming ages of these deposits should be later than that of the Habo alkaline intrusion.     

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

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