Sources and geodynamic setting of petrogenesis of the Middle Cambrian Upper Petropavlovka alkaline basic pluton (Kuznetsk Alatau,Siberia)

Early Paleozoic alkaline basic magmatism in the Kuznetsk Alatau is manifested in the Upper Petropavlovka pluton of gabbro, feldspathoid rocks (theralites, mafic foidolites, and nepheline syenites), and Ca-carbonatites. According to Sm–Nd and Rb–Sr isotope data, the pluton formed in the Middle Cambrian (509 ± 10 Ma). The silicate igneous rocks correspond in the contents of silica, alumina, and alkalies to derivates of a K–Na alkaline basic association. The Ca-carbonatites are characterized by a high-temperature (600–900 °C) paragenesis of apatite, clinopyroxene, ferromonticellite, phlogopite, and magnetite. They are enriched in P2O5 (up to 6.4 wt.%), Sr (up to 3000–4500 ppm; Sr/Ba ~ 5–7), and REE + Y (up to 800 ppm) and show evidence for liquation genesis. The predominant magmatic source (εNd(T) = 5–7) was moderately depleted PREMA, possibly combined with E-MORB and EM. According to the isotopic data ((87Sr/86Sr)T ~ 0.7024–0.7065; δ18O ~ 6.3–15.5‰; δ18C ~ –3.5 to –2.0‰), the fractionation of the melts was accompanied by their crustal contamination. The trace-element composition of the mafic rocks testifies to the participation of a substance similar to the substrata of the parental magmas of MORB, IAB, and OIB in the magma generation. This suggests intrusion in the geodynamic setting of interaction between the active continental margin and an ascending mantle diapir. Most likely, the intrusion led to the mixing of material from different sources, including the components of PREMA, enriched suprasubduction lithospheric mantle (EM), and continental crust. The assumption is made that the complexes of highly alkaline rocks and carbonatites in the western Central Asian Fold Belt are of plume origin and belong to an Early Paleozoic large igneous province.     

Deducing the source and composition of rare earth mineralising fluids in carbonatites: insights from isotopic (C,O, <Superscript>87</Superscript>Sr/<Superscript>86</Superscript>Sr) data from Kangankunde,Malawi

Carbonatites host some of the largest and highest grade rare earth element (REE) deposits but the composition and source of their REE-mineralising fluids remains enigmatic. Using C, O and ⁸⁷Sr/⁸⁶Sr isotope data together with major and trace element compositions for the REE-rich Kangankunde carbonatite (Malawi), we show that the commonly observed, dark brown, Fe-rich carbonatite that hosts REE minerals in many carbonatites is decoupled from the REE mineral assemblage. REE-rich ferroan dolomite carbonatites, containing 8–15 wt% REE₂O₃, comprise assemblages of monazite-(Ce), strontianite and baryte forming hexagonal pseudomorphs after probable burbankite. The ⁸⁷Sr/⁸⁶Sr values (0.70302–0.70307) affirm a carbonatitic origin for these pseudomorph-forming fluids. Carbon and oxygen isotope ratios of strontianite, representing the REE mineral assemblage, indicate equilibrium between these assemblages and a carbonatite-derived, deuteric fluid between 250 and 400 °C (δ¹⁸O + 3 to + 5‰_VSMOW and δ¹³C ? 3.5 to ? 3.2‰_VPDB). In contrast, dolomite in the same samples has similar δ¹³C values but much higher δ¹⁸O, corresponding to increasing degrees of exchange with low-temperature fluids (< 125 °C), causing exsolution of Fe oxides resulting in the dark colour of these rocks. REE-rich quartz rocks, which occur outside of the intrusion, have similar δ¹⁸O and ⁸⁷Sr/⁸⁶Sr to those of the main complex, indicating both are carbonatite-derived and, locally, REE mineralisation can extend up to 1.5 km away from the intrusion. Early, REE-poor apatite-bearing dolomite carbonatite (beforsite: δ¹⁸O + 7.7 to + 10.3‰ and δ¹³C ?5.2 to ?6.0‰; ⁸⁷Sr/⁸⁶Sr 0.70296–0.70298) is not directly linked with the REE mineralisation.     

Isotope and rare earth element chemistry of carbonatite–alkaline complexes of Deccan volcanic province: implications to magmatic and alteration processes

Results of different isotopic and trace element studies on three carbonatite–alkaline complexes (Amba Dongar, Mundwara and Sarnu-Dandali) of the Deccan flood basalt province, India, are presented. The Amba Dongar (Ambadungar) complex has been dated precisely to 65.0±0.3 Ma by the ⁴⁰Ar–³⁹Ar method. The minimum initial Sr isotopic ratio of alkaline rocks of Amba Dongar is found to be same as that of the coexisting carbonatites, suggesting their derivation from a common parent magma, probably through liquid immiscibility. The rare earth element abundance in these rocks also supports the liquid immiscibility hypothesis. Further investigation revealed that the parent magma of this complex has been contaminated (∼5%) by the lower crustal material, which is clearly reflected in the initial ⁸⁷Sr/⁸⁶Sr variation of alkaline rocks but not in the carbonatites. Sr study also suggests that the mantle source of Amba Dongar like the other two complexes is a Rb/Sr enriched source. The temporal and spatial relationships of all the three complexes with the Deccan flood basalts support the hypothesis of reunion plume origin for these. Fractional crystallization and subsequent hydrothermal/meteoric alteration are found to have controlled the stable carbon and oxygen isotopic variations in carbonatites. This study suggests that all the complexes have been derived from isotopically average mantle except for a particular batch of parent magma at Amba Dongar, which appears to have incorporated recycled crustal carbon. In a plume origin scenario such incorporation indicates the entrainment of ¹³C-enriched subcontinental lithospheric mantle by the plume.     

Isotope geochemistry (O, C, S, Sr) and Rb-Sr age of carbonatites in central Tuva

The Rb-Sr isochron age of igneous ankerite-calcite and siderite carbonatites in central Tuva is estimated at 118 ± 9 Ma. The following ranges of initial values of O, C, Sr, and sulfide and S isotopic compositions were established: δ¹⁸O_carb = +(8.8?14.7)‰, δ¹³C_carb = ?(3.6?4.9)‰, δ¹⁸O_quartz = +(11.6?13.7)‰, δ³⁴S_pyrite = +(0.3?1.1)‰, and (⁸⁷Sr/⁸⁶Sr)_i =0.7042?0.7048 for ankerite-calcite carbonatite and δ¹⁸O_sid = +(9.2?12.4)‰, δ¹³C_sid = ?(3.9?5.9)‰, δ¹⁸O_quartz = +(11.2?11.4)‰, δ³⁴S_pyrite = ?(4.4–1.8)‰, δ³⁴S_sulfate = +(8.6?14.5)‰, and (⁸⁷Sr/⁸⁶Sr)_i = 0.7042?0.7045 for siderite carbonatite. The obtained isotopic characteristics indicate that both varieties of carbonatites are cognate and their mantle source is comparable with the sources of Late Mesozoic carbonatites in the western Transbaikal region and Mongolia. The revealed heterogeneity of isotopic compositions of carbonatites is caused by their contamination with country rocks, replacement with hydrothermal celestine, and supergene alteration.     

Geochemistry and petrogenesis of carbonatites from South Nam Xe,Lai Chau area,northwest Vietnam

This paper presents a study of the petrography, mineral chemistry, geochemistry, and Sr–Nd–Pb–C–O isotope systematics of carbonatite dykes and associated rocks from the northeastern part of the Song Da intracontinental rift in South Nam Xe (northwest Vietnam) aimed at constraining the origin of the carbonatite magmas. The carbonatites are characterized by SiO₂ < 12.18 wt.% and by wide ranges in FeO, MgO and CaO content that define them as calciocarbonatite and ferrocarbonatite. On U–Th–Pb isochron diagrams, whole rocks and mineral separates from the ferrocarbonatites form linear arrays corresponding to ages of 30.2–31.6 Ma (Rupelian, Oligocene). The South Nam Xe carbonatites are extremely enriched in Sr, Ba, and light rare earth elements (LREE), and depleted in high field strength elements (HFSE) (e.g. Ti, Nb, Ta, Zr and Hf). The age–corrected Sr–Nd–Pb isotope ratios and C isotope data are relatively uniform (⁸⁷Sr/⁸⁶Sr_(t) = 0.708193–0.708349; ¹⁴³Nd/¹⁴⁴Nd_(t) = 0.512250–0.512267; ε_Nd(t) = ?6.46 to ?6.80; ²⁰⁶Pb/²⁰⁴Pb_(t) = 18.26–18.79; ²⁰⁷Pb/²⁰⁴Pb_(t) = 15.62–15.64; ²⁰⁸Pb/²⁰⁴Pb_(t) = 38.80–39.38; δ¹³C_V-PDB = –2.7?‰ to ?4.1?‰). These isotopic compositions indicate source contamination that occurred before the production of the carbonatite magmas, and did not change noticeably during or after emplacement. The variation in oxygen isotopes is consistent with the change in mineral compositions and trace element abundances: the lower δ¹⁸O values (9.1–11.0?‰) coupled with Sr-rich, Mn-poor calcite, and igneous textures such as triple junctions among calcite grain boundaries, define a magmatic origin. However, the elevated δ¹⁸O values of the ferrocarbonatites (12.0–13.3?‰) coupled with a volatile-bearing mineral assemblages (including REE fluorcarbonates, sulfates, sulfides and fluorite) may be due to interaction with meteoric water during low-temperature alteration. High δ¹³C values and Sr–Pb ratios, and low Rb/Sr (0.00014–0.00301), Sm/Nd (0.089–0.141) and ¹⁴³Nd/¹⁴⁴Nd ratios, coupled with very high Sr-Nd concentrations, suggest the involvement of an enriched mantle component, which probably resulted from metasomatism due to the migration of subducted material. Because of the lack of tectonic data and the limited number of samples studied, this conclusion is still ambiguous and requires further study.     

The age and petrologic and geochemical conditions of formation of the Kogtakh gabbro-monzonite complex in the Kuznetsk Alatau

We present new data on the U-Pb age of zircons, geochemistry of trace elements, and isotope (Nd, Sr, O) composition of rocks of the Kogtakh gabbro-monzonite complex on the eastern slope of the Kuznetsk Alatau Ridge. The established age of zircon in the rocks of the main intrusive phases (500-480 Ma) is taken as the time of formation of the Kogtakh complex in the Late Cambrian-Early Ordovician, during the accretion-collision stage of evolution of the Central Asian Orogenic Belt. The distribution and ratios of LILE and HFSE in the rocks suggest that the intrusions proceeded under interaction of the PREMA + EM/OIB mantle plume and the suprasubductional lithospheric IAB mantle. The mantle-crust interaction led to the heterogeneous isotopic composition of neodymium in the magma source (?_Nd(T) ~ 3.5-5.4). The mixing of different mantle and continental-crust materials resulted in an increase in isotope parameters: (⁸⁷Sr/⁸⁶Sr)_T ~ 0.7039-0.7052, ?_Sr(T) ~ 0-19, and δ¹⁸O ~ 6.5-8.8‰ (SMOW). The REE ratio in the least differentiated gabbroids indicates different depths of probable magma chambers and the formation of their primary (Tb/Yb_PM > 1.8) mafic melts at different degrees of melting of the model garnet peridotite.     

Zircon U-Pb age and Hf-O isotope insights into genesis of Permian Tarim felsic rocks,NW China: Implications for crustal melting in response to a mantle plume

Deciphering the contribution of crustal materials to A-type granites is critical to understanding their petrogenesis. Abundant alkaline syenitic and granitic intrusions distributed in Tarim Large Igneous Province, NW China, offer a good opportunity to address relevant issues. This paper presents new zircon Hf-O isotopic data and U-Pb dates on these intrusions, together with whole-rock geochemical compositions, to constrain crustal melting processes associated with a mantle plume. The ∼280 Ma Xiaohaizi quartz syenite porphyry and syenite exhibit identical zircon δ¹⁸O values of 4.40 ± 0.34‰ (2σ) and 4.48 ± 0.28‰ (2σ), respectively, corresponding to whole-rock δ¹⁸O values of 5.6‰ and 6.0‰, respectively. These values are similar to mantle value and suggest an origin of closed-system fractional crystallization from Tarim plume-derived melts. In contrast, the ∼275 Ma Halajun A-type granites have higher δ¹⁸O values (8.82–9.26‰) than the mantle. Together with their whole-rock ε_Nd(t) (−2.0–+0.6) and zircon ε_Hf(t) (−0.6–+1.5) values, they were derived from mixing between crust- and mantle-derived melts. These felsic rocks thus record crustal melting above the Tarim mantle plume. At ∼280–275 Ma, melts derived from decompression melting of Tarim mantle plume were emplaced into the crust, where fractional crystallization of a common parental magma generated mafic-ultramafic complex, syenite, and quartz syenite porphyry as exemplified in the Xiaohaizi region. Meanwhile, partial melting of upper crustal materials would occur in response to basaltic magma underplating. The resultant partial melts mixed with Tarim plume-derived basaltic magmas coupled with fractional crystallization led to formation of the Halajun A-type granites.     

Emplacement age and isotope geochemistry of Sung Valley alkaline–carbonatite complex, Shillong Plateau, northeastern India: implications for primary carbonate melt and genesis of the associated silicate rocks

The early Cretaceous (Albian–Aptian) Sung Valley ultramafic–alkaline–carbonatite complex is one of several alkaline intrusions that occur in the Shillong Plateau, India. This complex comprises calcite carbonatite and closely associated ultramafic (serpentinized peridotite, pyroxenite and melilitolite) and alkaline rocks (ijolite and nepheline syenite). Field relationship and geochemical characteristics of these rocks do not support a genetic link between carbonatite and associated silicate rocks. There is geochemical evidence that pyroxenite, melilitolite and ijolite of the complex are genetically related. Stable (C and O) and radiogenic (Nd and Sr) isotope data clearly indicate a mantle origin for the carbonatite samples. The carbonatite Nd (+0.7 to +1.8) and Sr (+4.7 to +7.0) compositions overlap the field for Kerguelen ocean island basalts. One sample of ijolite has Nd and Sr isotopic compositions that also plot within the field for Kerguelen ocean island basalts, whereas the other silicate–carbonatite samples indicate involvement with an enriched component. These geochemical and isotopic data indicate that the rocks of the Sung Valley complex were derived from and interacted with an isotopically heterogeneous subcontinental mantle and is consistent with interaction of a mantle plume (e.g. Kerguelen plume) with lithosphere. A U–Pb perovskite age of 115.1±5.1 Ma obtained for a sample of Sung Valley ijolite also supports a temporal link to the Kerguelen plume. The observed geochemical characteristics of the carbonatite rocks indicate derivation by low-degree partial melting (0.1%) of carbonated mantle peridotite. This melt, containing a substantial amount of alkali elements, interacted with peridotite to form metasomatic clinopyroxene and olivine. This process could progressively metasomatize lherzolite to form alkaline wehrlite.     

Strontium isotope systematics of Amba Dongar and Sung Valley carbonatite-alkaline complexes,India: evidence for liquid immiscibility,crustal contamination and long-lived Rb/Sr enriched mantle sources

The results of a Sr isotopic study of coexisting alkaline silicate rocks and carbonatites of two Cretaceous alkaline complexes of India, Amba Dongar (Deccan Flood Basalt Province) and Sung Valley (Rajmahal–Bengal–Sylhet Flood Basalt Province) are reported. The overlapping nature of initial Sr isotopic ratios of alkaline rocks and carbonatites of both the complexes is consistent with a magmatic differentiation model. Modelling of initial ⁸⁷Sr/⁸⁶Sr variation in alkaline rocks of Amba Dongar is consistent with a process of crustal assimilation by the parent magma undergoing simultaneous fractional crystallization of silicate rocks and silicate–carbonate melt immiscibility. A maximum of ∼5% crustal contamination has been estimated for the parent magma of Amba Dongar, the effect of which is not seen in the Sr isotope ratio of carbonatites generated by liquid immiscibility. A two point Rb–Sr isochron of the Sung Valley carbonatites, pyoxenite and a phlogopite from a carbonatite yielded an age of 106±11 Ma, which is identical to the ⁴⁰Ar–³⁹Ar age of this complex. The same age for the carbonatites and the alkaline silicate rocks, similar initial Sr ratios and the higher Sr concentration in the former than the latter favour the hypothesis of liquid immiscibility for the generation of the Sung Valley. The higher initial ⁸⁷Sr/⁸⁶Sr ratio for these complexes than that of the Bulk Earth indicates their derivation from long-lived Rb/Sr-enriched sources.     

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.     

Geochemistry of О, Н, C,S, and Sr isotopes in the water and sediments of the Aral basin

The paper presents original authors' data on the O, H, C, S, and Sr isotopic composition of water and sediments from the basins into which the Aral Sea split after its catastrophic shoaling: Chernyshev Bay (CB), the basin of the Great Aral in the north, Lake Tshchebas (LT), and Minor Sea (MS). The data indicate that the δ¹⁸О, δD, δ¹³C, and δ³⁴S of the water correlate with the mineralization (S) of the basins (as of 2014): for CB, S = 135.6‰, δ¹⁸О = 4.8 ± 0.1‰, δD = 5 ± 2‰, δ¹³C (dissolved inorganic carbon, DIC) = 3.5 ± 0.1‰, δ³⁴S = 14.5‰; for LT, S = 83.8‰, δ¹⁸О = 2.0 ± 0.1‰, δD =–13.5 ± 1.5‰, δ¹³C = 2.0 ± 0.1‰, δ³⁴S = 14.2‰; and for MS, S = 9.2‰, δ¹⁸О =–2.0 ± 0.1‰, δD =–29 ± 1‰, δ¹³C =–0.5 ± 0.5‰, δ³⁴S = 13.1‰. The oxygen and hydrogen isotopic composition of the groundwaters are similar to those in MS and principally different from the artesian waters fed by atmospheric precipitation. The mineralization, δ¹³С, and δ³⁴S of the groundwaters broadly vary, reflecting interaction with the host rocks. The average δ¹³С values of the shell and detrital carbonates sampled at the modern dried off zones of the basins are similar: 0.8 ± 0.8‰ for CB, 0.8 ± 1.4‰ for LT, and –0.4 ± 0.3‰ for MS. The oxygen isotopic composition of the carbonates varies much more broadly, and the average values are as follows: 34.2 ± 0.2‰ for CB, 32.0 ± 2.2‰ for LT, and 28.2 ± 0.9‰ for MS. These values correlate with the δ¹⁸O of the water of the corresponding basins. The carbonate cement of the Late Eocene sandstone of the Chengan Formation, which makes up the wave-cut terrace at CB, has anomalously low δ¹³С up to –38.5‰, suggesting origin near a submarine methane seep. The δ³⁴S of the mirabilite and gypsum (11.0 to 16.6‰) from the bottom sediments and young dried off zone also decrease from CB to MS in response to increasing content of sulfates brought by the Syr-Darya River (δ³⁴S = 9.1 to 9.9‰) and weakening sulfate reduction. The ⁸⁷Sr/⁸⁶Sr ratio in the water and carbonates of the Aral basins do not differ, within the analytical error, and is 0.70914 ± 0.00003 on average. This value indicate that the dominant Sr source of the Aral Sea is Mesozoic–Cenozoic carbonate rocks. The Rb–Sr systems of the silicate component of the bottom silt (which is likely dominated by eolian sediments) of MS and LT plot on the Т = 160 ± 5 Ma, I₀ = 0.7091 ± 0.0001, pseudochron. The Rb–Sr systems of CB are less ordered, and the silt is likely a mixture of eolian and alluvial sediments.     

Origin of Paleofluids in Dabashan Foreland Thrust Belt:Geochemical Evidence of 13C,18O and 87Sr/86Sr in Veins and Host Rocks

In the last ten years, with important discoveries from oil and gas exploration in the Dabashan foreland depression belt in the borderland between Shanxi and Sichuan provinces, the relationship between the formation and evolution of, and hydrocarbon accumulation in, this foreland thrust belt from the viewpoint of basin and oil and gas exploration has been studied. At the same time, there has been little research on the origin of fluids within the belt. Based on geochemical system analysis including Z values denoting salinity and research on δ13C, δ18O and 87Sr/86Sr isotopes in the host rocks and veins, the origin of paleofluids in the foreland thrust belt is considered. There are four principal kinds of paleofluid, including deep mantle-derived, sedimentary, mixed and meteoric. For the deep mantle-derived fluid, the δ13C is generally less than ?5.0‰PDB, δ18O less than -10.0‰PDB, Z value less than 110 and 87Sr/86Sr less than 0.70600; the sedimentary fluid is mainly marine carbonate-derived, with the δ13C generally more than ?2.0‰PDB, δ18O less than ?10.0‰PDB, Z value more than 120 and 87Sr/86Sr ranging from 0.70800 to 0.71000; the mixed fluid consists mainly of marine carbonate fluid (including possibly a little mantle-derived fluid or meteoric water), with the δ13C generally ranging from ?2.0‰ to ?8.0‰PDB, δ18O from ?10.0‰ to ?18.0‰ PDB, Z value from 105 to 120 and 87Sr/86Sr from 0.70800 to 0.71000; the atmospheric fluid consists mainly of meteoric water, with the δ13C generally ranging from 0.0‰ to ?10.0‰PDB, δ18O less than ?8.0‰PDB, Z value less than 110 and 87Sr/86Sr more than 0.71000. The Chengkou fault belt encompasses the most complex origins, including all four types of paleofluid; the Zhenba and Pingba fault belts and stable areas contain a simple paleofluid mainly of sedimentary type; the Jimingsi fault belt contains mainly sedimentary and mixed fluids, both consisting of sedimentary fluid and meteoric water. Jurassic rocks of the foreland depression belt contain mainly meteoric fluid.     

Petrogenesis and tectonic implications of early Silurian high-K calc-alkaline granites and their potassic microgranular enclaves,western Kunlun orogen,NW Tibetan Plateau

The western Kunlun orogen occupies a key position along the tectonic junction between the Pan-Asian and Tethyan domains, reflecting Proto- and Palaeo-Tethys subduction and terrane collision during early Palaeozoic to early Mesozoic time. We present the first detailed zircon U–Pb chronology, major and trace element, and Sr–Nd–O–Hf isotope geochemistry of the Qiukesu pluton and its microgranular enclaves from this multiple orogenic belt. SHRIMP zircon U–Pb dating shows that the Qiukesu pluton was emplaced in the early Silurian (ca. 435 Ma). It consists of weakly peraluminous high-K calc-alkaline monzogranite and syenogranite, with initial ⁸⁷Sr/⁸⁶Sr ratios of 0.7131–0.7229, ?_Nd(T) of –4.1 to –5.7, δ¹⁸O of 8.0–10.8‰, and ?_Hf(T) (in situ zircon) of –4.9. Elemental and isotopic data suggest that the granites formed by partial melting of lower-crustal granulitized metasedimentary-igneous Precambrian basement triggered by underplating of coeval mantle-derived enclave-forming intermediate magmas. Fractional crystallization of these purely crustal melts may explain the more felsic end-member granitic rocks, whereas such crustal melts plus additional input from coeval enclave-forming intermediate magma could account for the less felsic granites. The enclaves are intermediate (SiO₂ 57.6–62.2 wt.%) with high K₂O (1.8–3.6 wt.%). They have initial ⁸⁷Sr/⁸⁶Sr ratios of 0.7132–0.7226, ?_Nd(T) of –5.0 to –6.0, δ¹⁸O of 6.9–9.9‰, and ?_Hf(T) (in situ zircon) of –8.1. We interpret the enclave magmas as having been derived by partial melting of subduction-modified mantle in the P–T transition zone between the spinel and spinel-garnet stability fields. Our new data suggest that subduction of the Proto-Tethyan oceanic crust was continuous to the early Silurian (ca. 435 Ma); the final closure of the Proto-Tethys occurred in the middle Silurian.     

Riftogenic magmatism of western part of the Early Mesozoic Mongolian–Transbaikalian igneous province: Results of geochronological studies

Geochronological studies of rocks from a bimodal high-alkali volcanic–plutonic complex collected in the area of Kharkhorin zone of the Early Mesozoic Mongolian–Transbaikalian igneous province (MTIP) are made. The age of alkali granites from Olziit sum is 211 ± 1 Ma (U–Pb ID-TIMS on zircon) to 209 ± 2 and 217 ± 4 Ma (⁴⁰Ar/³⁹Ar on alkali amphibole); the age of alkali granite-porphyries from the area of Sant sum is 206 ± 1 Ma (U–Pb ID-TIMS on zircon). These rock series formed syncronously to the analogous magmatism episode in the Northern Gobi and Western Transbaikalian rift zones of the MTIP. The similarity of the age and composition of igneous associations of the MTIP suggests a common mechanism of its formation related to the effect of a mantle plume on the continental lithosphere at the base of the entire igneous zone having a zonal structure.     

Petrogenesis and tectonic implications of early Paleozoic granitoids in East Kunlun belt: Evidences from geochronology,geochemistry and isotopes

The East Kunlun Orogenic Belt(EKOB) provides an important link to reconstruct the evolution of the Proto-Tethys and Paleo-Tethys realm. The EKOB is marked by widespread Early Paleozoic magmatism.Here we report the petrology, bulk geochemistry, zircon Ue Pb dating and, Lue Hf and SreN d isotopic data of the Early Paleozoic granitic rocks in Zhiyu area of the southern EKOB. Based on the zircon U-Pb dating, these granitoids, consisting of diorite, granodiorite and monzogranite, were formed during 450 -430 Ma the Late Ordovician to Middle Silurian. The diorite and granodiorite are high Sr/Y ratio as adakitic affinities, and the monzogranite belongs to highly fractionated I-type. Their(~(87)Sr/~(86)Sr)ivalues range from 0.7059 to 0.7085, εNd(t) values from -1.6 to -6.0 and the zircon εHf(t) values show large variations from +9.1 to -8.6 with Hf model ages(T_(DM2)) about 848 Ma and 1970 Ma. The large variations of whole-rock Nd and zircon Hf isotopes demonstrate strong isotopic heterogeneity of the source regions which probably resulted from multi-phase underplating of mantle-derived magmas. Geochemical and isotopic studies proved that the diorite and granodiorite had been derived from partial melting of heterogeneous crustal source with variable contributions from ancient continental crust and juvenile components, and the monzogranites were representing fractional crystallization and crustal contamination for arc magma. The Early Paleozoic adakitic rocks and high-K calc-alkaline granitoids in the southern EKOB were likely emplaced in a continental marginal arc setting possibly linked to the southwards subduction of the Paleo Kunlun Ocean and the magma generation is linked to partial melting of thickened continental crust induced by underplating of mantle-derived magmas.     

S, C, O, H Isotope Data and Noble Gas Studies of the Maoniuping LREE Deposit, Sichuan Province, China： A Mantle Connection for Mineralization

The Maoniuping REE deposit, located about 22 km to the southwest of Mianning, Sichuan Province, is the second largest light REE deposit in China, subsequent to the Bayan Obo Fe-Nb-REE deposit in the Inner Mongolia Autonomous Region. Tectonically, it is located in the transitional zone between the Panxi rift and the Longmenshan-Jinpingshan orogenic zone. It is a carbonatite vein-type deposit hosted in alkaline complex rocks. The bastnaesite-barite, bastnaesite-calcite, and bastnaesite-microcline lodes are the main three types of REE ore lodes. Among these, the first lode is distributed most extensively and its REE mineralization is the strongest. Theδ34Sv-CDT values of the barites in the ore of the deposit vary in a narrow range of +5.0 to +5.1‰in the bastnaesite-calcite lode and +3.3 to +5.9‰in the bastnaesite-barite lode, showing the isotopic characteristics of magma-derived sulfur. Theδ13Cv-PDB values and theδ518OV-SMOW values in the bastnaesite-calcite lode range from -3.9 to -6.9‰and from +7.3 to +9.7‰, respectively, which fall into the range of "primary carbonatites", showing that carbon and oxygen in the ores of the Maoniuping deposit were derived mainly from a deep source. Theδ13Cv-PDB values of fluid inclusions vary from -3.0 to -5.6‰, with -3.0 to -4.0‰in the bastnaesite-calcite lode and -3.0 to -5.6‰in the bastnaesite-barite lode, which show characteristics of mantle-derived carbon. TheδDv-SMOW values of fluid inclusions range from -57 to -88‰, with -63 to -86‰in the bastnaesite-calcite lode and -57 to -88‰in the bastnaesite-barite lode, which show characteristics of mantle-derived hydrogen. Theδ18OH2OV-SMOW values vary from +7.4 to +8.6‰in the bastnaesite calcite lode, and +6.7 to +7.8‰in the bastnaesite-barite lode, almost overlapping the range of +5.5 to +9.5‰for magmatic water. The 4He content, R/Ra ratios are (13.95 to 119.58×10-6 (cm3/g)STP and 0.02 to 0.11, respectively, and 40Ar/36Ar is 313±1 to 437±2. Considering the 4He increase caused by high contents of radioactive elements, a mantle-derived fluid probably exists in the inclusions in the fluorite, calcite and bastnaesite samples. The Maoniuping deposit and its associated carbonatite-alkaline complex were formed in 40.3 to 12.2 Ma according to K-Ar and U-Pb data. All these data suggest that large quantities of mantle fluids were involved in the metallogenic process of the Maoniuping REE deposit through a fault system.     

In situ zircon U–Pb and Hf–O isotopic results for ca. 73 Ma granite in Hainan Island: Implications for the termination of an Andean-type active continental margin in southeast China

We report in the paper integrated analyses of in situ zircon U–Pb ages, Hf–O isotopes, whole-rock geochemistry and Sr–Nd isotopes for the Longlou granite in northern Hainan Island, southeast China. SIMS zircon U–Pb dating results yield a crystallization age of ∼73 Ma for the Longlou granite, which is the youngest granite recognized in southeast China. The granite rocks are characterized by high SiO₂ and K₂O, weakly peraluminous (A/CNK = 1.04–1.10), depletion in Sr, Ba and high field strength elements (HFSE) and enrichment in LREE and large ion lithophile elements (LILE). Chemical variations of the granite are dominated by fractional crystallization of feldspar, biotite, Ti–Fe oxides and apatite. Their whole-rock initial ⁸⁷Sr/⁸⁶Sr ratios (0.7073–0.7107) and ε_Nd(t) (−4.6 to −6.6) and zircon ε_Hf(t) (−5.0 to 0.8) values are broadly consistent with those of the Late Mesozoic granites in southeast China coast. Zircon δ¹⁸O values of 6.9–8.3‰ suggest insignificant involvement of supracrustal materials in the granites. These granites are likely generated by partial melting of medium- to high-K basaltic rocks in an active continental margin related to subduction of the Pacific plate. The ca. 73 Ma Longlou granite is broadly coeval with the Campanian (ca. 80–70 Ma) granitoid rocks in southwest Japan and South Korea, indicating that they might be formed along a common Andean-type active continental margin of east–southeast Asia. Tectonic transition from the Andean-type to the West Pacific-type continental margin of southeast China likely took place at ca.70 Ma, rather than ca. 90–85 Ma as previously thought.     

Genesis of the Bangbu Orogenic Gold Deposit,Tibet: Evidence from Fluid Inclusion,Stable Isotopes,and Ar-Ar Geochronology

The Bangbu gold deposit is a large orogenic gold deposit in Tibet formed during the AlpineHimalayan collision. Ore bodies(auriferous quartz veins) are controlled by the E-W-trending Qusong-Cuogu-Zhemulang brittle-ductile shear zone. Quartz veins at the deposit can be divided into three types: pre-metallogenic hook-like quartz veins, metallogenic auriferous quartz veins, and postmetallogenic N-S quartz veins. Four stages of mineralization in the auriferous quartz veins have been identified:(1) Stage S1 quartz+coarse-grained sulfides,(2) Stage S2 gold+fine-grained sulfides,(3) Stage S3 quartz+carbonates, and(4) Stage S4 quartz+ greigite. Fluid inclusions indicate the oreforming fluid was CO_2-N_2-CH_4 rich with homogenization temperatures of 170–261°C, salinities 4.34–7.45 wt% Na Cl equivalent. δ~(18)Ofluid(3.98‰–7.18‰) and low δDV-SMOW(-90‰ to-44‰) for auriferous quartz veins suggest ore-forming fluids were mainly metamorphic in origin, with some addition of organic matter. Quartz vein pyrite has δ~(34)SV-CDT values of 1.2‰–3.6‰(an average of 2.2‰), whereas pyrite from phyllite has δ~(34)SV-CDT 5.7‰–9.9‰(an average of 7.4‰). Quartz vein pyrites yield 206Pb/204 Pb ratios of 18.662–18.764, 207Pb/204 Pb 15.650–15.683, and ~(208)Pb/204 Pb 38.901–39.079. These isotopic data indicate Bangbu ore-forming materials were probably derived from the Langjiexue accretionary wedge. 40Ar/39 Ar ages for sericite from auriferous sulfide-quartz veins yield a plateau age of 49.52 ± 0.52 Ma, an isochron age of 50.3 ± 0.31 Ma, suggesting that auriferous veins were formed during the main collisional period of the Tibet-Himalayan orogen(~65–41 Ma).     

Age and geochemistry of the Newania dolomite carbonatites, India: implications for the source of primary carbonatite magma

The Newania carbonatite complex of India is one of the few dolomite-dominated carbonatites of the world. Intruding into Archean basement gneisses, the rocks of the complex have undergone limited diversification and are not associated with any alkaline silicate rock. Although the magmatic nature of the complex was generally accepted, its age of emplacement had remained equivocal because of the disturbed nature of radioisotope systems. Many questions about the nature of its mantle source and mode of origin had remained unanswered because of lack of geochemical and isotopic data. Here, we present results of our effort to date the complex using ¹⁴⁷Sm–¹⁴³Nd, ²⁰⁷Pb–²⁰⁶Pb and ⁴⁰Ar–³⁹Ar dating techniques. We also present mineral chemistry, major and trace element geochemistry and Sr–Nd isotopic ratio data for these carbonatites. Our age data reveal that the complex was emplaced at ~1,473 Ma and parts of it were affected by a thermal event at ~904 Ma. The older ²⁰⁷Pb–²⁰⁶Pb ages reported here (~2.4 Ga) and by one earlier study (~2.3 Ga; Schleicher et al. Chem Geol 140:261–273, 1997) are deemed to be a result of heterogeneous incorporation of crustal Pb during the post-emplacement thermal event. The thermal event had little effect on many magmatic signatures of these rocks, such as its dolomite–magnesite–ankerite–Cr-rich magnetite–magnesio-arfvedsonite–pyrochlore assemblage, mantle like δ¹³C and δ¹⁸O and typical carbonatitic trace element patterns. Newania carbonatites show fractional crystallization trend from high-Mg to high-Fe through high-Ca compositions. The least fractionated dolomite carbonatites of the complex possess very high Mg# (≥80) and have similar major element oxide contents as that of primary carbonatite melts experimentally produced from peridotitic sources. In addition, lower rare earth element (and higher Sr) contents than a typical calcio-carbonatite and mantle like Nb/Ta ratios indicate that the primary magma for the complex was a magnesio-carbonatite melt and that it was derived from a carbonate bearing mantle. The Sr–Nd isotopic data suggest that the primary magma originated from a metasomatized lithospheric mantle. Trace element modelling confirms such an inference and suggests that the source was a phlogopite bearing mantle, located within the garnet stability zone.     

New carbonatite complex in the western Baikal area,southern Siberian craton: Mineralogy,age, geochemistry,and petrogenesis

A dike–vein complex of potassic type of alkalinity recently discovered in the Baikal ledge, western Baikal area, southern Siberian craton, includes calcite and dolomite–ankerite carbonatites, silicate-bearing carbonatite, phlogopite metapicrite, and phoscorite. The most reliable ⁴⁰Ar–³⁹Ar dating of the rocks on magnesioriebeckite from alkaline metasomatite at contact with carbonatite yields a statistically significant plateau age of 1017.4 ± 3.2 Ma. The carbonatite is characterized by elevated SiO₂ concentrations and is rich in K₂O (K₂O/Na₂O ratio is 21 on average for the calcite carbonatite and 2.5 for the dolomite–ankerite carbonatite), TiO₂, P₂O₅ (up to 9 wt %), REE (up to 3300 ppm), Nb (up to 400 ppm), Zr (up to 800 ppm), Fe, Cr, V, Ni, and Co at relatively low Sr concentrations. Both the metapicrite and the carbonatite are hundreds of times or even more enriched in Ta, Nb, K, and LREE relative to the mantle and are tens of times richer in Rb, Ba, Zr, Hf, and Ti. The high (Gd/Yb)_CN ratios of the metapicrite (4.5–11) and carbonatite (4.5–17) testify that their source contained residual garnet, and the high K₂O/Na₂O ratios of the metapicrite (9–15) and carbonatite suggest that the source also contained phlogopite. The Nd isotopic ratios of the carbonatite suggest that the mantle source of the carbonatite was mildly depleted and similar to an average OIB source. The carbonatites of various mineral composition are believed to be formed via the crystallization differentiation of ferrocarbonatite melt, which segregated from ultramafic alkaline melt.