High Precision Sr‐Nd‐Hf‐Pb Isotopic Compositions of USGS Reference Material BCR‐2

The Lamont‐Doherty Earth Observatory radiogenic isotope group has been systematically measuring Sr‐Nd‐Pb‐Hf isotopes of USGS reference material BCR‐2 (Columbia River Basalt 2), as a chemical processing and instrumental quality control monitor for isotopic measurements. BCR‐2 is now a widely used geochemical inter‐laboratory reference material (RM), with its predecessor BCR‐1 no longer available. Recognising that precise and accurate data on RMs is important for ensuring analytical quality and for comparing data between different laboratories, we present a compilation of multiple digestions and analyses made on BCR‐2 during the first author's dissertation research. The best estimates of Sr, Nd and Hf isotope ratios and measurement reproducibilities, after filtering at the 2s level for outliers, were ⁸⁷Sr/⁸⁶Sr = 0.705000 ± 11 (2s, 16 ppm, n = 21, sixteen digestions, one outlier), ¹⁴³Nd/¹⁴⁴Nd = 0.512637 ± 13 (2s, 25 ppm, n = 27, thirteen digestions, one outlier) and ¹⁷⁶Hf/¹⁷⁷Hf = 0.282866 ± 11 (2s, 39 ppm, n = 25, thirteen digestions, no outliers). Mean Nd and Hf values were within error of those reported by Weis et al. (2006, 2007) in their studies of RMs; mean Sr values were just outside the 2s uncertainty range of both laboratories. Moreover, a survey of published Sr‐Nd‐Hf data shows that our results fall within the range of reported values, but with a smaller variability. Our Pb isotope results on acid leached BCR‐2 aliquots (n = 26, twelve digestions, two outliers) were ²⁰⁶Pb/²⁰⁴Pb = 18.8029 ± 10 (2s, 55 ppm), ²⁰⁷Pb/²⁰⁴Pb = 15.6239 ± 8 (2s, 52 ppm), ²⁰⁸Pb/²⁰⁴Pb = 38.8287 ± 25 (2s, 63 ppm). We confirm that unleached BCR‐2 powder is contaminated with Pb, and that sufficient leaching prior to digestion is required to achieve accurate values for the uncontaminated Pb isotopic compositions.     

In Situ U‐Th‐Pb Dating and Sr‐Nd Isotope Analysis of Bastnäsite by LA‐(MC)‐ICP‐MS

Bastnäsite is the end member of a large group of carbonate–fluoride minerals with the common formula (REE) CO₃F·CaCO₃. This group is generally widespread and, despite never occurring in large quantities, represents the major economic light rare earth element (LREE) mineral in deposits related to carbonatite and alkaline intrusions. Since bastnäsite is easily altered and commonly contains inclusions of earlier‐crystallised minerals, in situ analysis is considered the most suitable method to measure its U‐Th‐Pb and Sr‐Nd isotopic compositions. Electron probe microanalysis and laser ablation (multi‐collector) inductively coupled plasma‐mass spectrometry of forty‐six bastnäsite samples from LREE deposits in China, Pakistan, Sweden, Mongolia, USA, Malawi and Madagascar indicate that this mineral typically has high Th and LREE and moderate U and Sr contents. Analysis of an in‐house bastnäsite reference material (K‐9) demonstrated that precise and accurate U‐Th‐Pb ages could be obtained after common Pb correction. Moreover, the Th‐Pb age with its high precision is preferable to the U‐Pb age because most bastnäsites have relatively high Th rather than U contents. These results will have significant implications for understanding the genesis of endogenous ore deposits and formation processes related to metallogenic geochronology research.     

Tectono-magmatic evolution from accretion to collision in the southern margin of the Central Asian Orogenic BeltSCIEI北大核心CSCD

造山带演化及增生到碰撞的转变是板块构造与大陆动力学研究中的前沿科学问题。中亚造山带被认为是古亚洲洋长期俯冲-增生演化形成的显生宙最大的增生造山带,以发育巨量的面状展布的俯冲-增生相关的弧岩浆岩为特征。并且,由于中亚增生型造山带在潘吉亚最后聚合过程中发生弧弧(陆)碰撞,因此缺乏大规模且跨构造单元的碰撞相关的构造和变质等物质标志。显然,能否识别出大洋闭合期间碰撞作用的岩浆标志成为确定增生造山带增生过程终止的关键之一。本文系统研究确定:中亚造山带东南缘二叠纪到三叠纪钙碱性-碱钙性岩浆在空间分布上显示出由北西向南东迁移演化的特征;在岩浆性质上具有从二叠纪新生地壳来源的弧岩浆向早-中三叠世碰撞挤压背景下古老陆壳组分逐渐增多的高Sr/Y岩浆以及晚三叠世后造山伸展相关的A型花岗岩演化的特征。这些特征提供了俯冲-增生向碰撞造山演变的关键岩浆岩证据。结合区域资料,厘定出增生造山带最后碰撞相关的标志性岩浆为沿缝合带呈零星线性展布的增厚下地壳源区的高Sr/Y花岗岩类,构建了中亚造山带南缘从双向俯冲-增生到增生楔-增生楔碰撞及后造山伸展的三阶段构造-岩浆演化模型。系统对比研究,揭示出增生-碰撞相关的岩浆记录沿横向展布在中亚造山带南缘甘肃北山到吉林中部一带,表明碰撞挤压相关的岩浆作用在中亚造山带南缘具有一定的普适性。中亚造山带南缘从增生到碰撞的岩浆演化记录的厘定,证实显生宙最大的巨型增生造山带演化末期经历了碰撞造山作用,对进一步深入探索增生造山演化末期碰撞相关的标志性岩浆具有重要意义。     

Combined Trace Element and Pb-Nd-Sr-O Isotope Evidence for Recycled Oceanic Crust (Upper and Lower) in the Iceland Mantle Plume

We present the results of a comprehensive major element, traceelement and Sr–Nd–Pb–O isotopic study of post-glacialvolcanic rocks from the Neovolcanic zones on Iceland. The rocksstudied range in composition from picrites and tholeiites, whichdominate in the main rift systems, to transitional and alkalicbasalts confined to the off-rift and propagating rift systems.There are good correlations of rock types with geochemical enrichmentparameters, such as La/Sm and La/Yb ratios, and with long-termradiogenic tracers, such as Sr–Nd–Pb isotope ratios,indicating a long-lived enrichment/depletion history of thesource region. ⁸⁷Sr/⁸⁶Sr vs ¹⁴³Nd/¹⁴⁴Nd defines a negative array.Pb isotopes define well-correlated positive arrays on both ²⁰⁶Pb/²⁰⁴Pbvs ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb diagrams, indicating mixing ofat least two major components: an enriched component representedby the alkali basalts and a depleted component represented bythe picrites. In combined Sr–Nd–Pb isotopic spacethe individual rift systems define coherent mixing arrays withslightly different compositions. The enriched component hasradiogenic Pb (²⁰⁶Pb/²⁰⁴Pb > 19·3) and very similargeochemistry to HIMU-type ocean island basalts (OIB). We ascribethis endmember to recycling of hydrothermally altered upperbasaltic oceanic crust. The depleted component that is sampledby the picrites has unradiogenic Pb (²⁰⁶Pb/²⁰⁴Pb < 17·8),but geochemical signatures distinct from that of normal mid-oceanridge basalt (N-MORB). Highly depleted tholeiites and picriteshave positive anomalies in mantle-normalized trace element diagramsfor Ba, Sr, and Eu (and in some cases also for K, Ti and P),negative anomalies for Hf and Zr, and low ¹⁸O_olivine values(4·6–5·0) below the normal mantle range.All of these features are internally correlated, and we, therefore,interpret them to reflect source characteristics and attributethem to recycled lower gabbroic oceanic crust. Regional compositionaldifferences exist for the depleted component. In SW Icelandit has distinctly higher Nb/U (68) and more radiogenic ²⁰⁶Pb/²⁰⁴Pbratios (18·28–18·88) compared with the NErift (Nb/U 47; ²⁰⁶Pb/²⁰⁴Pb = 18·07–18·47).These geochemical differences suggest that different packagesof recycled oceanic lithosphere exist beneath each rift. A thirdand minor component with relatively high ⁸⁷Sr/⁸⁶Sr and ²⁰⁷Pb/²⁰⁴Pbis found in a single volcano in SE Iceland (Öræfajökullvolcano), indicating the involvement of recycled sediments inthe source locally. The three plume components form an integralpart of ancient recycled oceanic lithosphere. The slope in theuranogenic Pb diagram indicates a recycling age of about 1·5Ga with time-integrated Th/U ratios of 3·01. Surprisingly,there is little evidence for the involvement of North AtlanticN-MORB source mantle, as would be expected from the interactionof the Iceland plume and the surrounding asthenosphere in formof plume–ridge interaction. The preferential samplingof the enriched and depleted components in the off-rift andmain rift systems, respectively, can be explained by differencesin the geometry of the melting regions. In the off-rift areas,melting columns are truncated deeper and thus are shorter, whichleads to preferential melting of the enriched component, asthis starts melting deeper than the depleted component. In contrast,melting proceeds to shallower depths beneath the main rifts.The longer melting columns also produce significant amountsof melt from the more refractory (lower crustal/lithospheric)component. KEY WORDS: basalts; trace element and Sr, Nd, Pb, O isotope geochemistry; Iceland plume; isotope ratios; oceanic crustal recycling; partial melting; plume–ridge interaction     

Neoproterozoic granitic activities in the Xingdi plutons at the Kuluketage block,NW China: Evidence from zircon U–Pb dating,geochemical and Sr–Nd–Hf isotopic analyses

Neoproterozoic igneous rocks are widely distributed in the Kuluketage block along the northern margin of the Tarim Craton. However, the published literature mainly focuses on the ca. 800 Ma adakitic granitoids in the area, with the granites that intrude the 735–760 Ma mafic–ultramafic rocks poorly studied. Here we report the ages, petrography and geochemistry of two granites in the Xingdi mafic–ultramafic rocks, in order to construct a new view of the non-adakitic younger granites. LA-ICP-MS zircon U–Pb dating provided weighted mean ²⁰⁶Pb/²³⁸U ages of 743.0 ± 2.5 Ma for the No.I granite (G1) and 739.0 ± 3.5 Ma for the No.II granite (G2). A clear core-rim texture of similar age and a high zircon saturation temperature of ca. 849 ± 14 °C were observed for the No.I granite; in contrast, G2 has no apparent core-rim texture but rather inherited older zircons and a lower zircon saturation temperature of ca. 763 ± 17 °C. Geochemical analysis revealed that G1 is an alkaline A-type granite and G2 is a high-K calc-alkaline I-type granite. Both granites share similar geochemical characteristics of arc-related magmatic rocks and enriched Sr–Nd–Hf isotopes, likely due to their enriched sources or mixing with enriched magma. Whereas G1 and its host mafic rocks form typical bimodal intrusions of the same age and similar Sr–Nd–Hf isotope compositions, G2 is younger than its host mafic rocks and its Sr–Nd–Hf isotope composition indicates a lower crust origin. Although they exhibit arc-related geochemical features, the two granites likely formed in a rift setting, as inferred from thier petrology, Sr–Nd–Hf isotopes and regional tectonic evolution.     

川西北地区马脑壳金矿床的成矿年代学

沉积容岩微细浸染型（ＳＨＤＧ）金矿床（或称卡林型金矿床）,广泛分布于各大洲的许多古代和现代的地体（地块）周边,如美国的大盆及中国的黔西南和川西北的金矿床,是经济上非常重要的一种金矿类型。关于ＳＨＤＧ金矿床物质来源和成因一直存在着较大的争议,目前存在三...     

Deep subduction of mantle-derived garnet peridotites from the Su-Lu UHP metamorphic terrane in China

Garnet peridotites from the southern Su‐Lu ultra‐high‐pressure metamorphic (UHPM) terrane, eastern China, contain porphyroblastic garnet with aligned inclusions comprising a low‐P–T mineral assemblage (chlorite, hornblende, Na‐gedrite, Na‐phlogopite, talc, spinel and pyrite). Orthopyroxene porphyroblasts show fine exsolution lamellae of clinopyroxene and minor chromite. A clinopyroxene inclusion in garnet shows some orthopyroxene exsolution lamellae. Both the rims of porphyroblastic pyroxene and garnet and the matrix pyroxene and garnet crystallized at the expense of olivine. This is interpreted as a result of metasomatism of the peridotites by an SiO₂‐rich melt at UHP conditions. A chromian garnet further overgrew on the rims of the garnet. The X_Mg values (Mg/(Mg+Fe)) of porphyroblastic garnet decrease from core to rim and vary in different peridotite samples, while the compositions of both the porphyroblastic and the matrix pyroxene are similar in terms of Ca–Mg–Fe. The Mg‐rich cores of porphyroblastic garnet and orthopyroxene record high temperatures and pressures (c. 1000 °C, ≥5.1 GPa), whereas the matrix minerals, including the rims of porphyroblasts, record much lower P–T (c. 4.2 GPa, c. 760 °C). Sm–Nd data give apparent isochron ages of c. 380 Ma and negative ε_Nd(0) values (c.?9). These dates are considered meaningless due to isotopic disequilibrium between garnet cores and the rest of the rocks. The isotopic disequilibrium was probably caused by metasomatism of the peridotites by melt/fluids derived from the coevally subducted crustal materials. On the other hand, the Rb–Sr isotopic systems of phlogopite and clinopyroxene appear to have reached equilibrium and record a cooling age of c. 205 Ma. It is suggested that the garnet peridotites were originally emplaced into a low‐P–T environment prior to the c. 220 Ma continental collision, during which they were subducted together with crustal rocks to mantle depth and subjected to UHP metamorphism. An important corollary is that at least some of the coevally subducted crustal rocks in the Su‐Lu terrane have been subjected to peak metamorphism at P–T conditions much higher than presently estimated (≥2.7 GPa, ≤800 °C).     

Sr isotopes in the Orgueil CI meteorite: Chronology of early solar system hydrothermal activity

New Sr isotopic analyses and calculated formation ages of carbonates from the Orgueil CI meteorite are reported. Among the samples analyzed in this work, dolomites give the youngest formation ages and may have been deposited intermittently starting near the time of parent body formation and continuing for at least 30 Ma. The Sr isotope data also suggest that breunnerites (Fe-Mn-Mg carbonates) crystallized after dolomite formation. Leaching experiments on bulk meteorite samples provide evidence for a very mobile, water soluble Sr reservoir in Orgueil that is characterized by extremely radiogenic Sr (⁸⁷ Sr/⁸⁶ Sr≈ 0.81-0.82). This unsupported Sr reflects recent element redistribution, possibly at the time of parent body breakup recorded by the ∼ 10 Ma exposure age of Orgueil. The carbonate data in particular corroborate earlier indications that hydrothermal processes were among the earliest events to affect the CI parent body.     

用化学地层学研究新元古代地层划分和对比

随着传统地层学向多学科相互渗透的综合地层学方向的发展,笔者开展了湖北峡东地区新元古界震旦系和南华系的化学地层学研究。分别介绍了碳酸盐岩地层的稳定同位素和碎屑岩化学蚀变指数的研究方法和成果并依此提出新元古界划分和对比方案。震旦系碳酸盐岩中所获得的δ13C变化曲线和87Sr/86Sr比值与世界诸多剖面的变化曲线基本一致。南华系碎屑岩的化学蚀变指数(CIA)的特征是莲沱组下部CIA值为55~65(代表寒冷环境的CIA值),莲沱组上部CIA值则增至65~75(代表温湿环境),而莲沱组顶部两个样品的CIA值再次降为寒冷指数60~65;南沱组CIA值均为60~65,除了顶部(接近震旦系)的两个样品分别为69·4和70·9。上述CIA值的变化表明南华系以寒冷气侯为主,并且经历过“寒冷—温湿—寒冷”气候的演变条件下的沉积物。沉积相的多样性说明即使在“冰期”期间古构造、古地理环境对沉积物特征的影响依然存在。     

Plutonism in the Variscan Odenwald (Germany): from subduction to collision

 Latest Devonian to early Carboniferous plutonic rocks from the Odenwald accretionary complex reflect the transition from a subduction to a collisional setting. For ∼362 Ma old gabbroic rocks from the northern tectonometamorphic unit I, initial isotopic compositions (ε_Nd=+3.4 to +3.8;⁸⁷Sr/⁸⁶Sr =0.7035–0.7053;δ¹⁸O=6.8–8.0‰) and chemical signatures (e.g., low Nb/Th, Nb/U, Ce/Pb, Th/U, Rb/Cs) indicate a subduction-related origin by partial melting of a shallow depleted mantle source metasomatized by water-rich, large ion lithophile element-loaded fluids. In the central (unit II) and southern (unit III) Odenwald, syncollisional mafic to felsic granitoids were emplaced in a transtensional setting at approximately 340–335 Ma B.P. Unit II comprises a mafic and a felsic suite that are genetically unrelated. Both suites are intermediate between the medium-K and high-K series and have similar initial Nd and Sr signatures (ε_Nd=0.0 to –2.5;⁸⁷Sr/⁸⁶Sr=0.7044–0.7056) but different oxygen isotopic compositions (δ¹⁸O=7.3–8.7‰ in mafic vs 9.3–9.5‰ in felsic rocks). These characteristics, in conjunction with the chemical signatures, suggest an enriched mantle source for the mafic magmas and a shallow metaluminous crustal source for the felsic magmas. Younger intrusives of unit II have higher Sr/Y, Zr/Y, and Tb/Yb ratios suggesting magma segregation at greater depths. Mafic high-K to shoshonitic intrusives of the southern unit III have initial isotopic compositions (ε_Nd=–1.1 to –1.8;⁸⁷Sr/⁸⁶Sr =0.7054–0.7062;δ¹⁸O=7.2–7.6‰) and chemical characteristics (e.g., high Sr/Y, Zr/Y, Tb/Yb) that are strongly indicative of a deep-seated enriched mantle source. Spatially associated felsic high-K to shoshonitic rocks of unit III may be derived by dehydration melting of garnet-rich metaluminous crustal source rocks or may represent hybrid magmas. Received: 7 December 1998 / Accepted: 27 April 1999