Petrogenesis of mid-Carboniferous volcanics and granitic intrusions from western Junggar Basin boreholes: geodynamic implications for the Central Asian Orogenic Belt in Northwest China

The western Junggar Basin is located on the southeastern margin of the West Junggar terrane, Northwest China. Its sedimentary fill, magma petrogenesis, tectonic setting, and formation ages are important for understanding the Carboniferous tectonic evolution and continental growth of the Junggar terrane and the Central Asian Orogenic Belt. This paper documents a set of new zircon secondary ion mass spectrometry U–Pb geochronological and Hf isotopic data and whole-rock elemental and Sr–Nd isotopic analytical results for the Carboniferous strata and associated intrusions obtained from boreholes in the western Junggar Basin. The Carboniferous strata comprise basaltic andesite, andesite, and dacite with minor pyroclastic rocks, intruded by granitic intrusions with zircon secondary ion mass spectrometry U–Pb ages of 327–324 Ma. The volcanic rocks are calc-alkaline and show low high ε_Nd(t) values (5.3–5.6) and initial ⁸⁷Sr/⁸⁶Sr (0.703561–0.703931), strong enrichment in LREEs, and some LILEs and depletion in Nb, Ta, and Ti. Furthermore, they also display high (La/Sm)_N (1.36–1.63), Zr/Nb, and La/Yb, variable Ba/La and Ba/Th and constant Th/Yb ratios. These geochemical data, together with low Sm/Yb (1.18–1.38) and La/Sm (2.11–2.53) ratios, suggest that these volcanic rocks were derived from a 5–8% partial melting of a mainly spinel Iherzolite-depleted mantle metasomatized by slab-derived fluids and melts of some sediments in an island-arc setting. In contrast, the granitic intrusions represent typical adakite geochemical features of high Sr and low Y and Yb contents, with no significant Eu anomalies, high Mg#, and depleted ε_Nd(t) (5.6–6.4) and ε_Hf(t) (13.7–16.2) isotopic compositions, suggesting their derivation from partial melting of hot subducted oceanic crust. In combination with the previous work, the West Junggar terrane and adjacent western Junggar Basin are interpreted as a Mariana-type arc system driven by northwestward subduction of the Junggar Ocean, possibly with a tectonic transition from normal to ridge subduction commencing ca. at 331–327 Ma.     

Nd–Sr isotopic constraint to the formation of metatexite and diatexite migmatites,Higo metamorphic terrane,central Kyushu,Japan

ABSTRACT

Metatexite and diatexite migmatites are widely distributed within the upper amphibolite and granulite-facies zones of the Higo low-P/high-T metamorphic terrane. Here we report Nd–Sr isotopic and whole rock composition data from an outcrop in the highest-grade part of the granulite-facies zone, in which diatexite occurs as a 3 m-thick layer between 2 m-thick layers of stromatic-structured metatexite within pelitic gneiss. The metatexite has Nd–Sr isotopes and whole rock compositions similar to those of the gneiss, but the diatexite shows the reverse. The diatexite has a higher ε_Nd(t) and ¹⁴⁷Sm/¹⁴⁴Nd ratio (ε_Nd(t) = ?0.5; ¹⁴⁷Sm/¹⁴⁴Nd = 0.1636) than the gneiss (ε_Nd(t) = ?2.1; ¹⁴⁷Sm/¹⁴⁴Nd = 0.1287) and metatexite (ε_Nd(t) = ?3.1; ¹⁴⁷Sm/¹⁴⁴Nd = 0.1188). The (⁸⁷Sr/⁸⁶Sr)_initial and ⁸⁷Rb/⁸⁶Sr of the diatexite ((⁸⁷Sr/⁸⁶Sr)_initial = 0.70568; ⁸⁷Rb/⁸⁶Sr = 0.416) are lower than those of the gneiss ((⁸⁷Sr/⁸⁶Sr)_initial = 0.70857; ⁸⁷Rb/⁸⁶Sr = 1.13) and metatexite ((⁸⁷Sr/⁸⁶Sr)_initial = 0.70792; ⁸⁷Rb/⁸⁶Sr = 1.11). The metatexite and gneiss show enrichment of Th and depletion of P and Eu and have a similar chondrite-normalized REE pattern, which shows steep LREE–MREE-enriched and gently declining HREE patterns and negative Eu anomalies, whereas the diatexite shows enrichment of Sr and depletion of Th and Y, and exhibits gently declining LREE and steeply declining HREE pattern and weak Eu depletion. The metatexite migmatite is interpreted to have formed by in situ partial melting in which the melt did not migrate from the source, whereas the diatexite migmatite included an externally derived melt with a juvenile component. The Cretaceous high-temperature metamorphism of the Higo metamorphic terrane is interpreted to reflect emplacement of mantle-derived basalts under a volcanic arc along the eastern margin of the Eurasian continent, and mass transfer and advection of heat via hybrid silicic melts from the lower crust.     

Elemental mobility in subduction metamorphism: insight from metamorphic rocks of the Franciscan Complex and the Feather River ultramafic belt,California

The degree of element mobility in subduction metamorphism has generated much debate; some workers advocate considerable mobility during metamorphism, whereas others postulate minimal mobility. We assess this issue by examination of major and trace element concentrations and Pb-, Nd-isotopic data for 39 mafic metavolcanic rocks from the Franciscan subduction complex, related units of coastal California, and the Feather River ultramafic belt of the northern Sierra Nevada, California; these samples span a wide range of metamorphic grade. We conclude that these rocks, despite their metamorphism up to eclogite facies, preserve protolith major and trace elemental compositions and isotopic ratios, with the exception of some mobile large ion lithophile elements such as Ba, Pb, and to a smaller extent La, U, and Sr. Thus subduction metamorphism of these metabasalts occurred in a largely closed system. Lack of light rare earth element enrichment in the rocks demonstrates lack of chemical exchange with subducted metasediments. Relatively low SiO₂ content (<48 wt.%) of many of the metamorphic rocks and the lack of correspondence between silica depletion and metamorphic grade suggests that the silica depletion resulted from seafloor hydrothermal alteration before subduction. In spite of demonstrated mobility of Pb, and possible mobility of Nd, isotopic ratios of Pb and Nd were not modified during subduction metamorphism. In contrast to our results from metabasaltic rocks, our analysis of actinolite-rich rinds from high-grade Franciscan mélange blocks suggests some chemical exchange between metachert and the overlying mantle. The increasing enrichment in Ba and Pb with increasing metamorphic grade suggests that Ba- and Pb-rich fluids interacted more intensely with metabasalt at the higher grades of metamorphism. Comparison of these results with studies of the active Mariana forearc suggests that fluids interacting with the mantle wedge up-dip of the region of magma genesis are derived from subducting sediments overlying the down-going plate.     

小秦岭303号石英脉流体包裹体Rb—Sr,^40Ar—^39Ar成矿年龄测定

用石英流体包裹体Ｒｂ－Ｓｒ、＾４０Ａｒ－＾３９Ａｒ法测定了小秦岭３０３号石英脉的形成时代为石元古代。其流体包裹体属Ｈ２Ｏ＋ＣＯ２＋ＣａＣｌ型,盐度为６．５％－１２．９８％,ＣＯ２含量高,Ｎａ＾＋〉Ｋ＋。３０３号石英脉Ｒｂ－Ｓｒ等时线年龄为（２３８２±３３６）Ｍａ－（２２３４±４７）Ｍａ,（＾８７ｓＲ／＾８６Ｓｒ）ｉ为（０．７３５１±０．００１９）－（０．７４１６±０．０００４）,＾４０Ａｒ＾＾３９     

Petrology and Geochemistry of Post-Collisional Early Miocene Volcanism in the Karacada? Area (Central Anatolia, Turkey)

Early Miocene (ca.?21–18 Ma) volcanism in the Karacada? area comprises three groups of volcanic rocks: (1) calcalkaline suite (andesitic to rhyolitic lavas and their pyroclastics), (2) mildly-alkaline suite (alkali basalt, hawaiite, mugearite, benmoreite and trachydacite), and (3) a single trachyandesitic flow unit. Field observations, 40Ar/39Ar ages and geochemical data show that there was a progressive temporal transition from group 1 to 3 in a post-collisional tectonic setting. The calcalkaline suite rocks with medium-K in composition resemble those of subduction-related lavas, whereas the mildly-alkaline suite rocks having a sodic tendency (Na2O/K2O=1.5–3.2) resemble those of within-plate lavas. Incompatible element and Sr-Nd isotopic characteristics of the suites suggest that the lithospheric mantle beneath the Karacada? area was heterogeneously enriched by two processes before collision: (1) enrichment by subduction-related processes, which is important in the genesis of the calcalkaline volcanism, (2) enrichment by small degree melts from the astenosphere, which dominates the mildly alkaline volcanism. Perturbation of the enriched lithosphere by either delamination following collision and uplift or removal of the subducted slab following subduction and collision (i.e., slab breakoff) is the likely mechanism for the initiation of the post-collision volcanism.     

Coeval potassic and sodic calc-alkaline series in the post-collisional Hercynian Tanncherfi intrusive complex, northeastern Morocco: geochemical, isotopic and geochronological evidence

The post-collisional late Hercynian Tanncherfi intrusive complex (TIC) is part of a widespread intrusive episode in the Moroccan Meseta. The complex contains a wide range of rock types, from monzogabbros to monzogranites. Two distinct magmatic series are recognized: (1) a potassic (shoshonitic) series consisting of monzogabbros, quartz monzonites and monzogranites; and (2) a sodic (granodioritic) series represented by quartz monzodiorites and granodiorites. All the Tanncherfi plutonic rocks display similar spider-diagram profiles, with LILE and LREE enrichment and Nb, Ta, Ti depletion, which are typical of subduction-related magmas. Combined major, trace element compositions and Sr, Nd isotopic results indicate that the two series have been derived from a LILE- and LREE-enriched continental lithospheric mantle source, under different partial melting and/or depth conditions. Intrusion of the Tanncherfi rocks was not temporally related to subduction and the enrichment of their source is likely to be linked to preceding subduction events. The two series evolved by fractional crystallization, of clinopyroxene, plagioclase, hornblende, biotite, K-feldspar and accessories (Fe–Ti oxide minerals, titanite, apatite and zircon) for the potassic series while the sodic series combined fractional crystallization with assimilation of felsic magmas with lower Sr isotopic ratio than the more mafic term of the series, the quartz monzodiorite. The intrusion of the potassic magmas (344±6 Ma) marks a major change in the tectonic regime of eastern Meseta. These magmas intruded during post-thickening uplift and extension, both probably favored by convective thinning of the lithosphere. This model provides a reasonable mechanism for the genesis of other Hercynian intrusive complexes in Morocco.     

Metal sources of the Navan carbonate-hosted base metal deposit, Ireland: Nd and Sr isotope evidence for deep hydrothermal convection

Nd and Sr isotope analyses are presented for gangue mineral samples from the giant carbonate-hosted Navan Zn–Pb deposit, Ireland, and for rocks from which Navan metals may have been derived. Analysis of gangue minerals spanning the Navan paragenetic sequence reveals systematic evolution in the composition of the mineralising fluid. Early fluid represented by replacive dolomite exhibits the lowest initial ⁸⁷Sr/⁸⁶Sr ratio (0.7083–0.7086), closest to that of the host limestone and to Lower Carboniferous seawater, and the highest ¹⁴³Nd/¹⁴⁴Nd ratio (0.51161–0.51176). Later generations of dolomite, barite and calcite, which encompass sulphide precipitation, have higher initial ⁸⁷Sr/⁸⁶Sr ratios (maximum 0.7105) and lower initial ¹⁴³Nd/¹⁴⁴Nd ratios (minimum 0.51157). All samples have initial Nd isotope ratios that are too low to have been acquired only from the host limestone. Drill core samples of presumed Ordovician volcanic and sedimentary rocks from beneath the Navan orebody have ¹⁴³Nd/¹⁴⁴Nd and ⁸⁷Sr/⁸⁶Sr ratios at the time of mineralisation of 0.51184–0.51217 and 0.7086–0.7138, respectively. The data are interpreted to indicate mixing of sulphide-rich, limestone-buffered brine, with a metal-bearing hydrothermal fluid, which had passed through sub-Carboniferous rocks, consistent with published fluid inclusion and S isotope data. The ¹⁴³Nd/¹⁴⁴Nd ratio of this basement-derived fluid is too low to have been imparted by flow through the Devonian Old Red Sandstone, as required in models of regional fluid flow in response to Hercynian uplift. Irrespective of whether such regional fluid flow occurred, the hydrothermal Nd must have been derived from sub-Devonian rocks. These conclusions broadly support the hydrothermal convection cell model in which brines, ultimately of surface origin, penetrated to a depth of several kilometres, leaching metals from the rocks through which they passed. The data also support increasing depth of penetration of convection cells with time. Metals were subsequently precipitated in carbonate rocks at sites of mixing with cooler, sulphide-rich fluids. However, comparison of the Navan hydrothermal gangue Nd–Sr isotope data with data from Lower Palaeozoic rocks strongly suggests that the latter cannot alone account for the “basement” signature. As the Navan deposit lies immediately north of the Iapetus Suture, this suggests that the Laurentian margin includes Precambrian basement.     

Origin of salinity in a multilayered aquifer with high salinization vulnerability

The Kaluvelly watershed is a coastal area (Tamil Nadu, India) where water abstraction has resulted in a dramatic fall in the level of the water table and a piezometric depression in the most exploited aquifer, the Vanur aquifer. In addition, intensification/mechanization of agriculture may have affected the quality of recharge water. An initial hydrodynamic study showed that the Vanur aquifer is highly vulnerable to salinization due to potential seawater intrusion, and our aim was to determine the source of salinity recorded in the groundwater of this multilayered aquifer. Our approach involved the use of existing boreholes and of a moderate number of samples, with the aim of developing appropriate water resource management techniques. Major element, ¹⁸O/¹⁶O, ²H/¹H and ⁸⁷Sr/⁸⁶Sr, ratios were measured in rainwater, surface water and groundwater collected during five sampling campaigns over a 2‐year period. Geochemical data indicate that the Vanur aquifer is recharged and that small mixings between aquifers fluctuate according to monsoon intensity. There was no evidence of seawater intrusion. The range of recorded salinity originated mainly from water–rock interaction but a disconnection of some deeper parts of the aquifer was apparent. Strontium isotopic ratios in the recharge area suggest an anthropogenic influence, possibly related to fertilizer use. A high SO₄/Cl ratio was observed in the aquifer; in the deeper parts, the influence of a formation containing lignite is hypothesized, whereas near the surface, sulphate may partly originate from fertilizer use and fossil fuel combustion. Water isotopic data suggest that the origin of precipitation in this region has been unchanged for several hundreds or thousands of years. Copyright © 2011 John Wiley & Sons, Ltd.     

内蒙古白银都西群变质火山岩的钕、锶同位素研究

白银都西群主要由斜长角闪岩、变粒岩、长英片岩和条带状混合岩组成,是白银都西-白乃庙地体的重要组成部分,主要分布在内蒙古白乃庙铜(金)矿床东北白银都西一带。长期以来,由于缺乏可信的同位素年龄数据,该套岩层的归属,构造性质和形成机理尚不清楚。笔者首次对白银都西群斜长角闪岩的Nd和Sr同位素组成进行了测定,所获Sm-Nd同位素等时年龄为1394±46Ma(23),Nd初始比值为0.511 243±8(23)和εNd(T)=+7.9±2.1(23)。~(87)Sr/~(86)Sr和~(87)Rb/~(86)Sr比值分别为0.705 79—0.709 12和0.17—0.34,两者之间不存在任何相关关系。结合野外地质证据和岩相学特征,我们认为:白银都西群基性火山活动发生在中元古代,成岩物质来自亏损地幔源,成岩以后构造变动和变质热液活动致使Rb-Sr同位素体系受到严重干扰破坏。     

Sr isotope evolution during chemical weathering of granites -- impact of relative weathering rates of minerals

The Sr isotopic systematics in the weathering profiles of biotite granite and granite porphyry in southern Jiangxi Province were investigated. The results showed that during the chemical weathering of granites, remarked fractionation occurred between Rb and Sr. During the early stages of chemical weathering of granites, the released Sr/Si and Sr/Ca ratios are larger than those of the parent rocks, and the leaching rate of Sr is higher than those of Si, Ca, K, Rb, etc. Dynamic variations in relative weathering rates of the main Sr-contributing minerals led to fluctuation with time in 87Sr/86Sr ratios of inherent and released Sr in the weathering crust of granite. Successive weathering of biotite, plagioclase and K-feldspar made 87Sr/86Sr ratios in the weathering residues show such a fluctuation trend as to decrease first, increase, and then decrease again till they maintain stable. This work further indicates that when Sr isotopes are used to trace biogeochemical processes on both the catchment and global scales, one must seriously take account of the prefer-ential release of Sr from dissolving solid phase and the fluctuation of 87Sr/86Sr ratios caused by the variations of relative weathering rates of Sr-contributing minerals.