Geochronology,Geochemistry and Petrogenesis of Diabase Dyke Swarms in East Tianshan,Xinjiang, NW China

Diabase dyke swarms are widespread in the East Tianshan and Beishan regions. LA-ICP-MS zircon U-Pb ages of these diabase vary from 305 Ma to 278 Ma, showing that these dykes were formed during Late Carboniferous-Early Permian magmatism. All diabase samples are subalkali calc-alkali, characterized by slight LREE and LILEs enrichment, and weak negative Ti, Nb and Ta anomalies. The diabase samples have positive εNd(t) values (>+3), high Sr isotopic compositions (initial 87Sr/86Sr values=0.7030-0.7097), and large variation of Pb isotopic compositions, indicating they were derived from a deplete mantle source. Regional geology and geochemistry evidences indicate that these diabase dyke swarms were generated in a lithosphere extensional setting and had the same magma sources. Initial magmas may be a mixture of depleted asthenosphere mantle and enriched lithospheric mantle during rapid magma ascending.     

一种用于标定工业CT设备点云提取精度的配准及评价算法

基于工业CT测量数据的逆向建模技术广泛应用于军事、汽车制造、航空、航天等领域。目前,在基于工业CT点云数据的逆向重构精度验证和标定上,国内外缺少相关研究。本文提出了一种用于标定工业CT设备点云提取精度的配准及评价算法。基于CT扫描和三维光学扫描点云数据,在研究多种配准算法的基础上,总结手动选点粗配准和自动全局精配准相结合的配准算法:手动选择三个匹配点,利用坐标变换完成粗配准;用ICP算法完成自动精配准,并利用修正的Hausdorff距离为目标函数来评价配准结果。对基于七参数法和ICP算法的计算步骤做了详细说明,并赋以实例。最后,以自行设计的标准件为例,获得CT测量设备点云提取精度标定值,验证配准流程的适用性。      

陕西秦岭梁岩体LA ICP MS锆石U Pb年龄及其地质意义

三叠纪花岗岩在秦岭造山带广泛发育,直接记录了秦岭造山带演化过程中的重要信息。秦岭梁岩体位于秦岭造山带商丹缝合带北侧,岩性主要为石英二长斑岩,斑晶为钾长石,部分斑晶具有白色斜长石环边;基质主要由石英(25%)、斜长石(45%)、钾长石(10%)、黑云母(15%)、角闪石(5%)组成。秦岭梁岩体中的锆石自形程度好,具环带结构,显示岩浆锆石的特征,两个样品的LA ICP MS锆石U Pb同位素年龄分别为(2165±21) Ma和(2194±26) Ma,二者在误差范围内一致,表明该岩体的岩浆结晶年龄为晚三叠纪。秦岭梁岩体的岩浆结晶年龄与勉略洋壳向北俯冲的时间(248~200 Ma)一致,表明岩体的形成与勉略洋壳向北俯冲有密切联系;同时秦岭梁石英二长斑岩的地球化学特征显示其是洋壳俯冲时弧岩浆活动的产物。因此北秦岭地区勉略洋闭合时间和陆陆碰撞拼合时间应不早于216~219 Ma。     

High‐Precision Barium Isotope Measurements of Carbonates by MC‐ICP‐MS

This study presents a high‐precision method to measure barium (Ba) isotope compositions of international carbonate reference materials and natural carbonates. Barium was purified using chromatographic columns filled with cation exchange resin (AG50W‐X12, 200–400 mesh). Barium isotopes were measured by MC‐ICP‐MS, using a ¹³⁵Ba–¹³⁶Ba double‐spike to correct mass‐dependent fractionation during purification and instrumental measurement. The precision and accuracy were monitored by measuring Ba isotope compositions of the reference material JCp‐1 (coral) and a synthetic solution obtained by mixing NIST SRM 3104a with other matrix elements. The mean δ^137/134Ba values of JCp‐1 and the synthetic solution relative to NIST SRM 3104a were 0.21 ± 0.03‰ (2s, n = 16) and 0.02 ± 0.03‰ (2s, n = 6), respectively. Replicate measurements of NIST SRM 915b, COQ‐1, natural coral and stalagmite samples gave average δ^137/134Ba values of 0.10 ± 0.04‰ (2s, n = 18), 0.08 ± 0.04‰ (2s, n = 20), 0.27 ± 0.04‰ (2s, n = 16) and 0.04 ± 0.03‰ (2s, n = 20), respectively. Barium mass fractions and Ba isotopes of subsamples drilled from one stalagmite profile were also measured. Although Ba mass fractions varied significantly along the profile, Ba isotope signatures were homogeneous, indicating that Ba isotope compositions of stalagmites could be a potential tool (in addition to Ba mass fractions) to constrain the source of Ba in carbonate rocks and minerals.     

Ultrafast, > 50 Hz LA‐ICP‐MS Spot Analysis Applied to U–Pb Dating of Zircon and other U‐Bearing Minerals

LA‐ICP‐MS U–Pb detrital zircon studies typically analyse 50–200 grains per sample, with the consequent risk that minor but geologically important age components (e.g., the youngest detrital zircon population) are not detected, and higher abundance age components are misrepresented, rendering quantitative comparisons between samples impossible. This study undertook rapid U–Pb LA‐ICP‐MS analyses (8 s per 18–47 μm diameter spot including baseline and ablation) of zircon, apatite, rutile and titanite using an aerosol rapid introduction system (ARIS). As the ARIS resolves individual single pulses at fast sampling rates, spot analyses require a high repetition rate (> 50 Hz) so the signal does not return to baseline and mass sweep times (> 80 ms) that span several laser pulses (i.e., major undersampling of the signal). All rapid U–Pb spot analyses employed 250–300 pulses, repetition rates of 53–65 Hz (total ablation times of 4.1–5.7 s) and low fluence (1.75–2.5 J cm^?2), resulting in pit depths of ca. 15 μm. Zircon, apatite, rutile and titanite reference material data yield an accuracy and precision (2s) of < 1% for pre‐Cenozoic reference materials and < 2% for younger reference materials. We present a detrital zircon data set from a Neoproterozoic tillite where > 1000 grains were analysed in < 3 h with a precision and accuracy comparable to conventional LA‐ICP‐MS analytical protocols, demonstrating the rapid acquisition of huge detrital data sets.     

A New Interlaboratory Characterisation of Silicon,Rare Earth Elements and Twenty‐Two Other Trace Element Concentrations in the Natural River Water Certified Reference Material SLRS‐6 (NRC‐CNRC)

The natural river water reference material SLRS‐6 (NRC‐CNRC) is the newest batch of a quality control material routinely used in many international environmental laboratories. This work presents a nine‐laboratory compilation of measurements of major and trace element concentrations and their related uncertainties, unavailable in the NRC‐CNRC certificate (B, Cs, Li, Ga, Ge, Hf, Nb, P, Rb, Rh, Re, S, Sc, Se, Si, Sn, Th, Ti, Tl, W, Y, Y, Zr and REEs). Measurements were mostly made using inductively coupled plasma‐mass spectrometry. The results are compared with equivalent data for the last batch of the material, SLRS‐5, measured simultaneously with SLRS‐6 in this study. In general, very low concentrations, close to the quantification limits, were found in the new batch. The Sr isotopic ratio is also reported.     

Rare Earth Element Determination in Olivine by Laser Ablation‐Quadrupole‐ICP‐MS: An Analytical Strategy and Applications

Olivine offers huge, largely untapped, potential for improving our understanding of magmatic and metasomatic processes. In particular, a wealth of information is contained in rare earth element (REE) mass fractions, which are well studied in other minerals. However, REE data for olivine are scarce, reflecting the difficulty associated with determining mass fractions in the low ng g^?1 range and with controlling the effects of LREE contamination. We report an analytical procedure for measuring REEs in olivine using laser ablation quadrupole‐ICP‐MS that achieved limits of determination (LOD) at sub‐ng g^?1 levels and biases of ~ 5–10%. Empirical partition coefficients (D values) calculated using the new olivine compositions agree with experimental values, indicating that the measured REEs are structurally bound in the olivine crystal lattice, rather than residing in micro‐inclusions. We conducted an initial survey of REE contents of olivine from mantle, metamorphic, magmatic and meteorite samples. REE mass fractions vary from 0.1 to double‐digit ng g^?1 levels. Heavy REEs vary from low mass fractions in meteoritic samples, through variably enriched peridotitic olivine to high mass fractions in magmatic olivines, with fayalitic olivines showing the highest levels. The variable enrichment in HREEs demonstrates that olivine REE patterns have petrological utility.     

Measurements of Rare Earth Element and Other Element Mass Fractions in Environmental Reference Materials (NIST SRM 1646a,NIST SRM 1400, IAEA‐395 and IAEA‐450) by INAA,ICP‐AES and ICP‐MS

INAA, ICP‐AES and ICP‐MS were used to elementally characterise four environmental reference materials – NIST SRM 1646a (Estuarine Sediment), NIST SRM 1400 (Bone Ash), IAEA‐395 (Urban Dust) and IAEA‐450 (Algae). An analytical scheme consisting of the three methods was first applied to NIST SRM 1646a to validate the methodology because it has been extensively analysed and has certified values for many elements. With repeated analyses of NIST SRM 1646a, the accuracy and measurement repeatability of the data obtained were evaluated based on two statistical calculations (zeta‐score and Horwitz ratio) and were observed to be good enough for the analytical scheme to be applied to similar sorts of environmental/geochemical samples. Applying the same approach to NIST SRM 1400, IAEA‐395 and IAEA‐450, enabled mass fractions of 29, 38 and 28 elements to be determined, respectively. Among these results, the data for rare earth elements are of particular interest, not only for IAEA‐450 but also for the other three reference samples. The data for Pr, Gd, Dy, Ho, Er and Tm in NIST SRM 1646a are newly reported in this study. By using small test portions (< 100 mg) for NIST SRM 1646a and IAEA‐395, and recommended minimum amounts for NIST SRM 1400 and IAEA‐450, sample homogeneity was evaluated.     

Development of Two New Copper Isotope Standard Solutions and their Copper Isotopic Compositions

In this study, two new laboratory reference solutions for testing Cu isotopic composition were established and investigated. Two commercially available pure copper products, copper plate and copper wire, were dissolved in 1000‐ml Teflon^® bottles, to produce 200 μg ml^?1 stock solutions (hereafter referred to as NWU‐Cu‐A and NWU‐Cu‐B), and cryogenically stored. The Cu isotopic compositions of the two samples were determined in three different laboratories using multi‐collector inductively coupled plasma‐mass spectrometry, and the Cu isotopic compositions obtained from the standard‐sample bracketing method were consistent within the two standard deviation (2s) range. The Cu isotopic compositions of the NWU‐Cu‐A and NWU‐Cu‐B standard solutions were δ⁶⁵Cu = +0.91 ± 0.03‰ (2s, n = 42) and δ⁶⁵Cu = ?0.05 ±0.03‰ (2s, n = 49), respectively, relative to the reference material NIST SRM 976.     

Quadrupole ICP‐MS: Introduction to Instrumentation,Measurement Techniques and Analytical Capabilities

The low detection limits and multi‐element capability of inductively coupled plasma‐mass spectrometry (ICP‐MS) makes it an attractive option in a wide range of environmental, medical, biological, industrial and archaeological applications. Quadrupole ICP‐MS is used to determine element concentrations in a diverse range of sample types, often very different from the geological applications for which ICP‐MS was originally developed. Whilst modern instruments are robust and capable of a high degree of automation, it is essential that users of both instrumentation and data are aware of the strengths and limitations of the technique. Many people who are now involved with the operation and application of ICP‐MS instruments are not specialists in the field, as was usually the case amongst early operators. This back‐to‐basics review is aimed at the novice user and includes a guide to ICP‐MS instrumentation and performance. Whilst solids, liquids and gases can all be measured by ICP‐MS, discussion of sample introduction is limited to liquids. Requirements for producing good quality data, including aspects of sample preparation, calibration, and methods of interference limitation are also discussed.