Geochemical and Petrological Studies on the Early Carboniferous Sidingheishan Mafic–Ultramafic Iintrusion in the Southern Margin of the Central Asian Orogenic Belt, NW China

The Sidingheishan mafic-ultramafic intrusion is located in the eastern part of the Northern Tianshan Mountain, along the southern margin of the Central Asian Orogenic Belt in northern Xinjiang autonomous region of China. The Sidingheishan intrusion is mainly composed of wehrlite, olivine websterite, olivine gabbro, gabbro and hornblende gabbro. At least two pulses of magma were involved in the formation of the intrusion. The first pulse of magma produced an olivine-free unit and the second pulse produced an olivine-bearing unit. The magmas intruded the Devonian granites and granodiorites.An age of 351.4±5.8 Ma(Early Carboniferous) for the Sidingheishan intrusion has been determined by U-Pb SHRIMP analysis of zircon grains separated from the olivine gabbro unit. A U-Pb age of 359.2±6.4 Ma from the gabbro unit has been obtained by LA-ICP-MS. Olivine of the Sidingheishan intrusion reaches 82.52 mole% Fo and 1414 ppm Ni. On the basis of olivine-liquid equilibria, it has been calculated that the MgO and FeO included in the parental magma of a wehrlite sample were approximately10.43 wt% and 13.14 wt%, respectively. The Sidingheishan intrusive rocks are characterized by moderate enrichments in Th and Sm, slight enrichments in light REE, and depletions in Nb, Ta, Zr and Hf. The ε_(Nd)(t) values in the rock units vary from +6.70 to +9.64, and initial ~(87)Sr/~(86)Sr ratios range between 0.7035 and0.7042. Initial ~(206)Pb/~(204)Pb, ~(207)Pb/~(204)Pb and ~(208)Pb/~(204)Pb values fall in the ranges of 17.23-17.91,15.45-15.54 and 37.54-38.09 respectively. These characteristics are collectively similar to the Heishan intrusion and the Early Carboniferous subduction related volcanic rocks in the Santanghu Basin, North Tianshan and Beishan area. The low(La/Gd)_(PM) values between 0.26 and 1.77 indicate that the magma of the Sidingheishan intrusion was most likely derived from a depleted spinel-peridotite mantle.(Th/Nb)_(PM)ratios from 0.59 to 20.25 indicate contamination of the parental magma in the upper crust.Crystallization modeling methods suggest that the parental magma of the Sidingheishan intrusion was generated by flush melting of the asthenosphere and subsequently there was about 10 vol%contamination from a granitic melt. This was followed by about 5 vol% assimilation of upper crustal rocks. Thus, the high-Mg basaltic parental magma of Sidingheishan intrusion is interpreted to have formed from partial melting of the asthenosphere during the break-off of a subducted slab.     

The Magma-dynamic Mechaism of Emplacement and Compositional Zonation of the Zhoukoudian Stock, Beijing

The Zhoukoudian stock in Beijing is a concentric zoned complex intrusive body formed by two successive intrusions. Quartz-diorite formed by the first intrusion is scattered sparsely on the margins of the body, while granodiorite resulting from the second intrusion constitutes the main part of the intrusion. It exhibits three distinct petrographic zones macroscopically, and is chemically characterized by enrichment of high-temperature components, such as Mg, Ca, Sc, Ti, Cr, Mn. Fe and Co, on its border and merely slight enrichment of some low-temperature components, such as Na and Si, in its central part. A series of structural features indicate that the deformation of the intrusion and thermo-metamorphic rocks becomes weaker with an increase of distance from the contact, and that the intrusive body is a product of ballooning or inflating diapiric emplacement. Based on calculations of the density, viscosity and yield strength of magma and the reasonable diffusion constants and oxygen isotopic data, the mechanism of the compositional zonation of the major part of the stock is discussed. It is considered that the Soret effect, combined with double-diffusive convection, can explain the compositional zonation of the intrusion. Calculation of the ascent rates of magma shows that successive upwelling of magma got faster and faster with the progress of time.     

Geological Relationships Between the Intrusions,Country Rocks,and Ni-Cu-PGE Sulfides of the Kharaelakh Intrusion,Noril′sk Region:Implications for the Roles of Sulfide Differentiation and Metasomatism in Their Genesis

The Ni-Cu-platinum group element sulfide ore deposits of the Kharaelakh Intrusion,Noril′sk Region,Siberia,represent a large concentration of sulfides associated with a small differentiated intrusion formed at the edge of the Siberian Craton in the roots of the Siberian Trap flood basalt.The deposit is associated with an intrusion that occupies a flanking periclinal structure adjacent to the Noril′sk-Kharaelakh Fault.The intrusion is strongly differentiated and comprises taxitic gabbrodolerites,picritic gabbrodolerites,and gabbrodolerites within the main body which in turn forms a chonolith within a sheet-like intrusion that extends laterally to form extensive undifferentiated sills of gabbrodolerite.The intrusion substantially replaces the stratigraphy of the country rocks,and although it appears to have exploited the axis of structures developed in response to transtension,the intrusion has created space by both mechanical dilation of stratigraphy and magmatic replacement of pre-existing sedimentary rocks.The frontal lobes of the main intrusion have complex apophyses of gabrodolerite on a range of scales that demonstrate replacement of the sedimentary rocks and link to the development of an extensive metamorphic halo in the country rocks.This halo is much narrower over the main body of the intrusion,and these observations have implications for the thermal history of the intrusion.Mg-skarns and breccias are developed in the roof of the main body of the intrusion.Within the intrusion,the taxitic rocks contain vesicles and the blebby sulfides developed in the picritic and taxitic gabbrodolerites appear to have a linkage to volatile phases.Cuprous sulfide mineralization developed at the roof of the Kharaelakh Intrusion is associated with metamorphosed and skarn-bearing country rocks,and appears to have been generated by a combination of sulfide fractionation and associated metasomatism.The geological relationships appear consistent with a chonolith model for the development of the differentiated intrusion and mineralization,but the extent of metasmorphism of the country rocks appears to be related to the unusual thickness of gabbrodolerite apophyses at the flanks of the intrusion rather than metamorphism produced by the passage of mafic magma through the intrusion.Variations in disseminated sulfide compositions and metasomatic textures in the skarns are described,and a model is proposed which balances traditional views on the evolution of the magma conduits with the impact of magmatic fluids transported through the magma column(i.e.transmagmatic fluids).The importance of structures in controlling the nature of the conduit,and the resultant small intrusions with excess sulfide is a feature of many other Ni-Cu sulfide deposits including Voisey′s Bay,and it is suggested that the sulfides are more likely to have beentransported from depth into their final resting place rather than developed by in-situ equilibration of sulfide with fresh magma in the chonolith.     

The Thermal History of the Huangmeijian Granite Intrusion in Anhui and Its Relation to Mineralization: Isotopic Evidence

Whole-rock Rb-Sr, zircon U-Pb and hornblende, biotite and K-feldspar K-Ar ages areused to reconstruct the cooling history of the Huangmeijian intrusion in the Anqing-Lujiangquartz-syenite belt in Anhui. Oxygen isotope geothermometry of mineral pairs demonstrates thatdiffusion is a dominant factor controlling the closure of isotopic systems. Assuming the coolingof the intrusion is synchronous with a dicrease in local geothermal gradients, an emplacementdepth of about 8 km and the magma crystallization temperature of 800±50℃ are estimated. TheHuangmeijian intrusion experienced a rapid cooling process and uplifted after its emplacementand crystallization at 133 Ma B.P. with a cooling rate of 34.5℃/Ma and an uplifting rate of 0.35mm/a. The intrusion was rising until it rested at a depth of 3km at a temperature of 300±50℃about 14 Ma later. Then the intrusion was in slow cooling and uplifting with a cooling rate of4.4℃/Ma and an uplifting rate of 0.04 mm/a. U-Pb dating of pitchblende is done for the hydrothermal uranium deposit formed in thecontact zone of the Huangmeijian intrusion. The result shows that the mineralization age is closeto the closing time of the K-Ar system in biotite. The fluid inclusion thermometry indicates thatthe mineralization temperature is in agreement with the closure temperature of the biotite K-Arsystem. This suggests a close relationship between the slow cooling of the intrusion and thehydrothermal uranium mineralization process.     

SHRIMP U-Pb Zircon Age of the Ka''erjiao Intrusion in the Sawur Region in West Junggar,Xinjiang

Acid intrusions are widespread in the Sawur region, Xinjiang. The Ka'erjiao intrusion is mainly composed of albite granite porphyry, K-feldspar granite porphyry, ivernite and granite porphyry. Being a transitional product between magma intrusion and eruption in the Sawur region, the Ka'erjiao intrusion was formed at the telophase of the late Carboniferous to the begining of early Permian as determined by the SHRIMP U-Pb zircon dating, with an age of 302.6±7.6 Ma (1σ). The intrusion consists of alkali-enriched rock, whose REE distribution patterns are of the LREE enrichment type, theδEu value is low and Nd, Sr, Pb isotopes reflect its mantle source characteristics. Theδ18O value of intrusion is low as a result of isotope exchange with meteoric water. The geochemical characteristics show that it was formed in a post-collisional tectonic setting. Taking combined considerations of current studies of A-type granites and Permian volcanic rocks, we think that in the telophase of the late Carboniferous to the beginning of the early Permian, the Sawur region was within the extension or compressional to extensional period of a post-collisional stage. The Ka'erjiao intrusion from mantle sources can confirm the vertical continental crust growth in the late Paleozoic. The Sawur region in west Junggar is consistent with east Junggar in post-collisional tectonic evolution process.     

SHRIMP U-Pb Zircon Age of the Ka''erjiao Intrusion in the Sawur Region in West Junggar,Xinjiang

Acid intrusions are widespread in the Sawur region, Xinjiang. The Ka'erjiao intrusion is mainly composed of albite granite porphyry, K-feldspar granite porphyry, ivernite and granite porphyry. Being a transitional product between magma intrusion and eruption in the Sawur region, the Ka'erjiao intrusion was formed at the telophase of the late Carboniferous to the begining of early Permian as determined by the SHRIMP U-Pb zircon dating, with an age of 302.6±7.6 Ma (1σ). The intrusion consists of alkali-enriched rock, whose REE distribution patterns are of the LREE enrichment type, theδEu value is low and Nd, Sr, Pb isotopes reflect its mantle source characteristics. Theδ18O value of intrusion is low as a result of isotope exchange with meteoric water. The geochemical characteristics show that it was formed in a post-collisional tectonic setting. Taking combined considerations of current studies of A-type granites and Permian volcanic rocks, we think that in the telophase of the late Carboniferous to the beginning of the early Permian, the Sawur region was within the extension or compressional to extensional period of a post-collisional stage. The Ka'erjiao intrusion from mantle sources can confirm the vertical continental crust growth in the late Paleozoic. The Sawur region in west Junggar is consistent with east Junggar in post-collisional tectonic evolution process.     

The Late Early Cretaceous Mo Mineralization in the South China Mo Province: Constraints from U–Pb and Re–Os Geochronology of the Lufeng Porphyry Mo Deposit

Compared to other Mo provinces, few studies focused on the South China Mo Province(SCMP), especially for Early Cretaceous Mo mineralization. The Lufeng porphyry Mo deposit in the SCMP is characterized by disseminated and veinlet-type mineralization in granite porphyry, gneiss, and rhyolite. In this study, six molybdenite samples yield a Re–Os isochron age of 108.0±1.8 Ma, which is consistent with the zircon U–Pb age of the granite porphyry(108.4±0.8 Ma). The coincidence of magmatic and hydrothermal activities indicates that Mo mineralization was associated with the intrusion of granite porphyry during the late Early Cretaceous. A compilation of U–Pb and Re–Os chronological data suggests that an extensive and intensive Mo mineralization event occurred in the SCMP during the late Early Cretaceous. The marked difference in molybdenite Re contents between Cu-bearing(85–536 ppm) and Cu-barren(1.3–59 ppm) Mo deposits of the late Early Cretaceous indicates that the ore-forming materials were derived from strong crust–mantle interactions. Together with regional petrological and geochemical data, this study suggests that late Early Cretaceous Mo mineralization in the SCMP occurred in an extensional setting associated with the roll-back of the Paleo-Pacific slab.     

SHRIMP U-Pb Zircon Age of the Ka''''erjiao Intrusion in the Sawur Region in West Junggar,Xinjiang

Acid intrusions are widespread in the Sawur region, Xinjiang. The Ka'erjiao intrusion is mainly composed of albite granite porphyry, K-feldspar granite porphyry, ivernite and granite porphyry. Being a transitional product between magma intrusion and eruption in the Sawur region, the Ka'erjiao intrusion was formed at the telophase of the late Carboniferous to the begining of early Permian as determined by the SHRIMP U-Pb zircon dating, with an age of 302.6±7.6 Ma (1σ). The intrusion consists of alkali-enriched rock, whose REE distribution patterns are of the LREE enrichment type, theδEu value is low and Nd, Sr, Pb isotopes reflect its mantle source characteristics. Theδ18O value of intrusion is low as a result of isotope exchange with meteoric water. The geochemical characteristics show that it was formed in a post-collisional tectonic setting. Taking combined considerations of current studies of A-type granites and Permian volcanic rocks, we think that in the telophase of the late Carboniferous to the beginning of the early Permian, the Sawur region was within the extension or compressional to extensional period of a post-collisional stage. The Ka'erjiao intrusion from mantle sources can confirm the vertical continental crust growth in the late Paleozoic. The Sawur region in west Junggar is consistent with east Junggar in post-collisional tectonic evolution process.     

Petrogenesis of the diamondiferous Pipe-8 ultramafic intrusion from the Wajrakarur kimberlite field of Southern India and its relation to the worldwide Mesoproterozoic(～1.1 Ga) magmatism of kimberlite and related rocks

Detailed mineralogy,bulk rock major,trace and Sr-Nd isotope compositions,and ~(40)Ar/~(39)Ar dating of the Pipe-8 diamondiferous ultramafic intrusion in the Wajrakarur cluster of southern India,is reported.Based on the presence of Ti-rich phlogopite,high Na/K content in amphibole,Al-and Ti-rich diopside,a titanomagnetite trend in spinel and the presence of Ti-rich schorlomite garnet and carbonates in the groundmass,the Pipe-8 intrusion is here more precisely classified as an ultramafic lamprophyre(i.e.,aillikite).An aillikite affinity of the Pipe-8 intrusion is further supported by the bulk rock major and trace element and Sr-Nd isotope geochemistry.Sr-Nd isotope data are consistent with a common,moderately depleted upper mantle source region for both the Pipe-8 aillikite as well as the Wajrakarur kimberlites of southern India.A phlogopite-rich groundmass ~(40)Ar/~(39)Ar plateau age of 1115.8±7.9 Ma(2σ) for the Pipe-8 intrusion falls within a restricted 100 Ma time bracket as defined by the 1053-1155 Ma emplacement ages of kimberlites and related rocks in India.The presence of ultramafic lamprophyres,carbonatites,kimberlites,and olivine lamproites in the Wajrakarur kimberlite field requires low degrees of partial melting of contrasting metasomatic assemblages in a heterogeneous sub-continental lithospheric mantle.The widespread association of kimberlite and other mantle-derived magmatism during the Mesoproterozoic(ca.1.1 Ga) have been interpreted as being part of a single large igneous province comprising of the Kalahari,Australian,West Laurentian and Indian blocks of the Rodinia supercontinent that were in existence during its assembly.In India only kimberlite/lamproite/ultramafic lamprophyre magmatism occurred at this time without the associated large igneous provinces as seen in other parts of Rodinia.This may be because of the separated paleo-latitudinal position of India from Australia during the assembly of Rodinia.It is speculated that the presence of a large plume at or close to 1.1 Ga within the Rodinian supercontinent,with the Indian block located on its periphery,could be the reason for incipient melting of lithospheric mantle and the consequent emplacement of only kimberlites and other ultramafic,volatile rich rocks in India due to comparatively low thermal effects from the distant plume.     

Seawater Intrusion in the Longkou-Laizhou Area, Shandong

The extensive intrusion (covering an area of 83.7-238.3 km~2 and accounting for 18.6-31.5% of the total area of the plain), the presence of a transitional zone 1.5-6.0 km in width, and the interconnection in distribution between the seawater intrusion district and the region lower than the sea level caused by the strong drop of the groundwater level are major characteristics of the seawater intrusion in the study area. Cation exchange played an important role during the formation of chemical composition of the groundwater in the seawater intrusion district.     

Study on the Cu–As–Sb–Ag–Bi–Pb–Te Sulfosalt Minerals from the Hydrothermal System of Southwestern Hokkaido,Japan

Shin‐Otoyo, Suttsu, Teine, Date, Chitose, and Koryu are sites rich in precious and base metal Miocene–Pleistocene epithermal deposits, and located in southwestern Hokkaido, Japan. The deposits are predominantly hosted by the Green Tuff Formation of Middle Miocene age. Ore petrographic study of these deposits shows the occurrence of variable quantities of Cu–As–Sb–Ag–Bi–Pb–Te sulfosalt minerals. Determination of mineralogical and chemical compositions of the sulfosalt minerals was undertaken to elucidate the time and spatial changes of the sulfide‐sulfosalt minerals. Various types of sulfosalt minerals identified from gold–silver and base metal quartz–sulfide veins represented some sulfosalt mineralization phases, such as the Cu–Fe–Sn–S phase of mawsonite and stannite; Cu–(As,Sb)–S phase of tetrahedrite–tennantite and luzonite–famatinite series minerals; (Cu,Ag)–Bi–Pb–S phase of emplectite, pavonite, friedrichite, aikinite, and lillianite–gustavite series minerals; (Ag,Cu)–(As,Sb)–S phase of proustite–pyrargyrite and pearceite–polybasite series minerals; and Bi–Te–S phase of tetradymite and kawazulite minerals. There are some trends in the paragenetic sequence of sulfosalt mineralization in southwestern Hokkaido (in complete or partial) as follows: sulfide → Cu–Fe–Sn–S → (Cu,Ag)–Bi–Pb–S → (Bi–Te–S) → Cu–(As,Sb)–S → ([Ag,Cu]–[As,Sb]–S). The formation of sulfosalt minerals is characterized by the introduction of some elements such as Sn, Bi, and Te at an earlier stage and an increase or decrease of some elements such as As and Sb, followed by the introduction of Ag at the later stage of ore mineral paragenesis sequence. Mineral composition of the Chitose and Koryu deposits are slightly different from those of Shin‐Otoyo, Suttsu, Teine, and Date due to their lack of Sn (tin) and Bi (bismuth) mineralization. The variable concentrations and relationships are not simply with redistributed trace elements from the original sulfide minerals of chalcopyrite, pyrite, galena, and sphalerite. Some heavier elements were also introduced during the replacement reaction, which is consistent with the occurrence of their associated minerals.     

An enlarged and updated internally consistent thermodynamic dataset with uncertainties and correlations: the system K2O–Na2O–CaO–MgO–MnO–FeO–Fe2O3–Al2O3–TiO2–SiO2–C–H2–O2

We present, as a progress report, a revised and much enlarged version of the thermodynamic dataset given earlier (Holland & Powell, 1985). This new set includes data for 123 mineral and fluid end-members made consistent with over 200 P–T–X_CO2–f_O2 phase equilibrium experiments. Several improvements and advances have been made, in addition to the increased coverage of mineral phases: the data are now presented in three groups ranked according to reliability; a large number of iron-bearing phases has been included through experimental and, in some cases, natural Fe:Mg partitioning data; H₂O and CO₂ contents of cordierites are accounted for with the solution model of Kurepin (1985); simple Landau theory is used to model lambda anomalies in heat capacity and the Al/Si order–disorder behaviour in some silicates, and Tschermak-substituted end-members have been derived for iron and magnesium end-members of chlorite, talc, muscovite, biotite, pyroxene and amphibole. For the subset of data which overlap those of Berman (1988), it is encouraging to find both (1) very substantial agreement between the two sets of thermodynamic data and (2) that the two sets reproduce the phase equilibrium experimental brackets to a very similar degree of accuracy. The main differences in the two datasets involve size (123 as compared to 67 end-members), the methods used in data reduction (least squares as compared to linear programming), and the provision for estimation of uncertainties with this dataset. For calculations on mineral assemblages in rocks, we aim to maximize the information available from the dataset, by combining the equilibria from all the reactions which can be written between the end-members in the minerals. For phase diagram calculations, we calculate the compositions of complex solid solutions (together with P and T) involved in invariant, univariant and divariant assemblages. Moreover we strongly believe in attempting to assess the probable uncertainties in calculated equilibria and hence provide a framework for performing simple error propagation in all calculations in thermocalc, the computer program we offer for an effective use of the dataset and the calculation methods we advocate.     

Outokumpu revisited: New mineral deposit model for the mantle peridotite-associated Cu–Co–Zn–Ni–Ag–Au sulphide deposits

The metaturbidites of the Palaeoproterozoic Jormua–Outokumpu thrust belt in eastern Finland enclose m- to km-scale ultramafic massifs that are distributed over an area of more than 5000 km². These bodies, which almost entirely consist of highly depleted mantle peridotites (now metaserpentinites and metaperidotites), are intimately associated with massive to semimassive, polymetallic Cu–Co–Zn–Ni–Ag–Au sulphide deposits that sustained mining in the region between 1913 and 1988. Currently, one deposit (Kylylahti) is proceeding into a definitive feasibility study emphasising the renewed economic interest for Outokumpu-type deposits.The origin of these Outokumpu-type Cu–Co–Zn–Ni–Ag–Au deposits is now re-interpreted to be polygenetic. First, their formation requires deposition of a Cu-rich proto-ore within peridotitic sea floor at  1950 Ma. Close modern analogues to the proto-ore setting include, for example, the Logatchev and Rainbow fields at the Mid-Atlantic Ridge, where venting of high-T–low-pH hydrothermal fluid resulted in accumulations of Cu–Zn–Co–Ag–Au sulphides on serpentinised ultramafic seafloor. Second, the Ni-rich composition of Outokumpu sulphide ores calls for a separate source for nickel: Some 40 Ma after the deposition of the Cu-rich proto-ore – concomitant with the obduction of the ultramafic massifs – disseminated Ni sulphides formed through chemical interaction between obducting peridotite massifs and adjacent black schists. This process was related to listwaenite–birbirite type carbonate–silica alteration at margins of the ultramafic massifs. Due to this alteration, silicate nickel was released from the primary Fe–Mg silicates and redeposited as Ni sulphides in the alteration fringes of the massifs.We propose that syntectonic mixing of these two “end-member” sulphides, i.e., the primary Cu-rich proto-ore and the secondary Ni-sulphide disseminations, resulted in the uncommon metal combination of the Outokumpu-type sulphides. Late tectonic solid-state re-mobilisation, related to the duplexing of the ore by isoclinal folding, upgraded the sulphides into economic deposits.     

Calculation of partial melting equilibria in the system Na2O–CaO–K2O–FeO–MgO–Al2O3–SiO2–H2O (NCKFMASH)

A thermodynamic model for haplogranitic melts in the system Na₂O–CaO–K₂O–Al₂O₃–SiO₂–H₂O (NCKASH) is extended by the addition of FeO and MgO, with the data for the additional end‐members of the liquid incorporated in the Holland & Powell (1998) internally consistent thermodynamic dataset. The resulting dataset, with the software thermocalc , is then used to calculate melting relationships for metapelitic rock compositions. The main forms for this are P–T and T–X pseudosections calculated for particular rock compositions and composition ranges. The relationships in these full‐system pseudosections are controlled by the low‐variance equilibria in subsystems of NCKFMASH. In particular, the solidus relationships are controlled by the solidus relationships in NKASH, and the ferromagnesian mineral relationships are controlled by those in KFMASH. However, calculations in NCKFMASH allow the relationships between the common metapelitic minerals and silicate melt to be determined. In particular, the production of silicate melt and melt loss from such rocks allow observations to be made about the processes involved in producing granulite facies rocks, particularly relating to open‐system behaviour of rocks under high‐grade conditions.     

Internally consistent data for sulphur‐bearing phases and application to the construction of pseudosections for mafic greenschist facies rocks in Na2O–CaO–K2O–FeO–MgO–Al2O3–SiO2–CO2–O–S–H2O

The Holland and Powell internally consistent data set version 5.5 has been augmented to include pyrite, troilite, trov (Fe_0.875S), anhydrite, H₂S, elemental S and S₂ gas. Phase changes in troilite and pyrrhotite are modelled with a combination of multiple end‐members and a Landau tricritical model. Pyrrhotite is modelled as a solid solution between hypothetical end‐member troilite (trot) and Fe_0.875S (trov); observed activity–composition relationships fit well to a symmetric formalism model with a value for w_trot?trov of ?3.19 kJ mol^?1. The hypothetical end‐member approach is required to compensate for iron distribution irregularities in compositions close to troilite. Mixing in fluids is described with the van Laar asymmetric formalism model with a_ij values for H₂O–H₂S, H₂S–CH₄ and H₂S–CO₂ of 6.5, 4.15 and 0.045 kJ mol^?1 respectively. The derived data set is statistically acceptable and replicates the input data and data from experiments that were not included in the initial regression. The new data set is applied to the construction of pseudosections for the bulk composition of mafic greenschist facies rocks from the Golden Mile, Kalgoorlie, Western Australia. The sequence of mineral assemblages is replicated successfully, with observed assemblages predicted to be stable at X(CO₂) increasing with increasing degree of hydrothermal alteration. Results are compatible with those of previous work. Assemblages are insensitive to the S bulk content at S contents of less than 1 wt%, which means that volatilization of S‐bearing fluids and sulphidation are unlikely to have had major effects on the stable mineral assemblage in less metasomatized rocks. The sequence of sulphide and oxide phases is predicted successfully and there is potential to use these phases qualitatively for geobarometry. Increases in X(CO₂) stabilized, in turn, pyrite–magnetite, pyrite–hematite and anhydrite–pyrite. Magnetite–pyrrhotite is predicted at temperatures greater than 410 °C. The prediction of a variety of sulphide and oxide phases in a rock of fixed bulk composition as a function of changes in fluid composition and temperature is of particular interest because it has been proposed that such a variation in phase assemblage is produced by the infiltration of multiple fluids with contrasting redox state. The work presented here shows that this need not be the case.     

Geochronology of the Limu W–Sn–Nb–Ta‐Bearing Granite Pluton in South China

Limu W–Sn–Nb–Ta mining district is located in the Nanling Range W–Sn poly‐metallic mineralization belt in south China. The district includes a number of Sn–Nb–Ta and W–Sn ore occurrences; all of them are spatially associated with granite stocks of a largely‐unexposed pluton, the Limu granitic pluton. A granite sample collected from the Sn–Nb–Ta‐bearing Jinzhuyuan granite stock yields a zircon SHRIMP U–Pb age of 218.3 ± 2.4 Ma, a muscovite ⁴⁰Ar/³⁹Ar plateau age of 212.4 ± 1.4 Ma, and a muscovite ⁴⁰Ar/³⁹Ar isochron age of 213.2 ± 2.2 Ma. Another granite sample collected from the W–Sn‐bearing Sangehuangniu granite stock yields a zircon SHRIMP U–Pb age of 214 ± 5 Ma. The geochronological data provide new constraints on the age of the Limu granite pluton and the timing of the associated W–Sn–Nb–Ta mineralization—at least it sets a reasonable upper age limit for the mineralization of the W–Sn–Nb–Ta ores. The reported ages suggest an active Late Triassic granitic magmatism in Limu area which is part of a regional magmatic event near the end of the Indosinian orogeny in south China.     

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

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

Composition and origin of intermediate solid solutions in the system thorite–xenotime–zircon–coffinite

A comprehensive survey of the accessory-mineral assemblages in Variscan granites of the German Erzgebirge and Pan-African granites from Jordan revealed the occurrence of intermediate solid solutions of the tetragonal thorite–xenotime–zircon–coffinite mineral group with partially novel compositions. These solid solutions preferentially formed in evolved and metasomatically altered, P-poor leucogranites of either I- or A-type affinity. Thorite from the Erzgebirge contained up to 18.8 wt.% Y₂O₃, 16.1 wt.% ZrO₂, and 23.3 wt.% UO₂. Xenotime and zircon have incorporated Th in abundances up to 36.3 wt.% and 41.8 wt.% ThO₂, respectively. Extended compositional gradation with only minor gaps is confined to hydrated members of this mineral group, and is observed to exist between thorite and xenotime, thorite and coffinite, and Y–HREE-bearing thorite and zircon. Complex, hydrous solid solutions containing elevated abundances of three or more of the endmembers are subordinate. Previously reported intermediate solid solutions between anhydrous zircon and xenotime, and anhydrous zircon and thorite, are not observed and are in conflict with experimental work demonstrating very limited miscibility between anhydrous species of endmember composition. The majority of hydrous intermediate solid solutions in the Th–Y–Zr–U system are likely thermodynamically unstable. Instead, they are probably metastable responses to unusual physico-chemical conditions involving various parameters and conditions, the relative importance of which is incompletely known. Leaching and dissolution of preexisting accessory phases during interaction with F-bearing hydrous fluids enriched in Th, Y(HREE), Zr, and/or U, and common deposition of the various elements at disequilibrium (supersaturation) seems to play a key role, but other processes may be of similar importance. Experimental work involving hydrous conditions and complex systems composed of more than two endmembers are needed to shed light into the stability relations of the chemically uncommon compositions treated in this study.     

The metapelitic garnet–biotite–muscovite–aluminosilicate–quartz (GBMAQ) geobarometer

In this contribution we have empirically calibrated the garnet–biotite–muscovite–aluminosilicate–quartz (GBMAQ) barometer using low- to medium–high-pressure, mid-grade metapelites. Application of the barometer suggests that the GBMAQ and GASP barometers show quite similar pressure estimates. Furthermore, metapelites within thermal contact aureole or very limited geographic area show no meaningful pressure diversity determined by the GBMAQ and GASP barometers which is the geological reality. The random error of the GBMAQ barometer is expected to be around ± 0.8 kbar, and this barometer shows no systematic bias with respect to either pressure, or temperature, or Al^VI in muscovite, or Fe in biotite, or Fe in garnet. The GBMAQ barometer is thermodynamically consistent with the garnet–biotite geothermometer because they share the same activity models of both garnet and biotite. This barometer is especially useful for assemblages with Ca-poor garnet or Ca-poor plagioclase or plagioclase-absent metapelites. Application of this barometer beyond the calibration ranges, i.e., P–T range and chemical ranges of the minerals, is not encouraged.     

Calibration of the garnet–biotite–Al2SiO5–quartz geobarometer for metapelites

A garnet–biotite–Al₂SiO₅–quartz (GBAQ) geobarometer was empirically calibrated using more than 700 natural metapelites with a broad compositional range of garnet and biotite under P–T conditions of 450–950°C and 1–17 kbar. In the calibration, activity models of garnet and biotite identical to those in the garnet–biotite (GB) geothermometer of Holdaway [American Mineralogist 2000, 85: 881–892] were used. Therefore, the GBAQ geobarometer and the GB geothermometer can be simultaneously applied to iteratively estimate metamorphic P–T conditions. Successful applications of the GBAQ geobarometer to natural metapelites certify its validity. Most importantly, when plagioclase is absent or CaO components in garnet and/or plagioclase are deficient, this geobarometer may prove useful for estimating metamorphic pressures. The random error of the present GBAQ geobarometer is inferred to be around ±1.8 kbar. An electronic spreadsheet is available as Table S4 to apply the GBAQ geobarometer in combination with the GB geothermometer.