西昆仑库地北依莎克群玄武岩锆石U-Pb年龄、地球化学特征及构造意义     

白春东  专少鹏  王金贵  李典  张新征  陈圆圆  张子轩 《地质论评》2018,64(2):498-508

西昆仑山分为北昆仑古生代复合沟弧带和南昆仑地块,依莎克群的形成时代和构造归属一直存在争议,库地蛇绿岩的形成时代亦无定论。本文运用电子探针微区成分分析和锆石U-Pb测年方法,对库地北西奴山依莎克群底部玄武岩中锆石进行了分析。获得依莎克群玄武岩中锆石LA-ICP-MS U-Pb年龄为519.5±1.2Ma,说明依莎克群玄武岩形成时代为中寒武世。与库地蛇绿岩构造环境和形成时代对比表明依莎克群玄武岩是库地蛇绿岩的组成部分,是原特提斯洋俯冲消减作用的产物。综合前人的年代学资料和本文成果表明库地蛇绿岩形成时代为中寒武世—晚寒武世。  相似文献   

Assessment of Nanosecond Laser Ablation Multi‐Collector Inductively Coupled Plasma‐Mass Spectrometry for Pb and Sr Isotopic Determination in Archaeological Glass: Mass Bias Correction Strategies and Results for Corning Glass Reference Materials          下载免费PDF全文

Alicia Van Ham‐Meert  Stepan M. Chernonozhkin  Stijn J.M. Van Malderen  Thibaut Van Acker  Frank Vanhaecke  Patrick Degryse 《Geostandards and Geoanalytical Research》2018,42(2):223-238

This work presents an evaluation of various methods for in situ high‐precision Sr and Pb isotopic determination in archaeological glass (containing 100–500 μg g^?1 target element) by nanosecond laser ablation multi‐collector‐inductively coupled plasma‐mass spectrometry (ns‐LA‐MC‐ICP‐MS). A set of four soda‐lime silicate glasses, Corning A–D, mimicking the composition of archaeological glass and produced by the Corning Museum of Glass (Corning, New York, USA), were investigated as candidates for matrix‐matched reference materials for use in the analysis of archaeological glass. Common geological reference materials with known isotopic compositions (USGS basalt glasses BHVO‐2G, GSE‐1G and NKT‐1G, soda‐lime silicate glass NIST SRM 610 and several archaeological glass samples with known Sr isotopic composition) were used to evaluate the ns‐LA‐MC‐ICP‐MS analytical procedures. When available, ns‐LA‐MC‐ICP‐MS results for the Corning glasses are reported. These were found to be in good agreement with results obtained via pneumatic nebulisation (pn) MC‐ICP‐MS after digestion of the glass matrix and target element isolation. The presence of potential spectral interference from doubly charged rare earth element (REE) ions affecting Sr isotopic determination was investigated by admixing Er and Yb aerosols by means of pneumatic nebulisation into the gas flow from the laser ablation system. It was shown that doubly charged REE ions affect the Sr isotope ratios, but that this could be circumvented by operating the instrument at higher mass resolution. Multiple strategies to correct for instrumental mass discrimination in ns‐LA‐MC‐ICP‐MS and the effects of relevant interferences were evaluated. Application of common glass reference materials with basaltic matrices for correction of ns‐LA‐MC‐ICP‐MS isotope data of archaeological glasses results in inaccurate Pb isotope ratios, rendering application of matrix‐matched reference materials indispensable. Correction for instrumental mass discrimination using the exponential law, with the application of Tl as an internal isotopic standard element introduced by pneumatic nebulisation and Corning D as bracketing isotopic calibrator, provided the most accurate results for Pb isotope ratio measurements in archaeological glass. Mass bias correction relying on the power law, combined with intra‐element internal correction, assuming a constant ⁸⁸Sr/⁸⁶Sr ratio, yielded the most accurate results for ⁸⁷Sr/⁸⁶Sr determination in archaeological glasses  相似文献   

Determination of In and Sn Mass Fractions in Sixteen Geological Reference Materials by Isotope Dilution MC‐ICP‐MS          下载免费PDF全文

Maria Kirchenbaur  Alexander Heuser  Alessandro Bragagni  Frank Wombacher 《Geostandards and Geoanalytical Research》2018,42(3):361-377

Mass fractions of Sn and In were determined in sixteen geological reference materials including basaltic/mafic (BCR‐2, BE‐N, BHVO‐1, BHVO‐2, BIR‐1, OKUM, W‐2, WS‐E), ultramafic (DTS‐2b, MUH‐1, PCC‐1, UB‐N) and felsic/sedimentary reference materials (AGV‐2, JA‐1, SdAR‐M2, SdAR‐H1). Extensive digestion and ion exchange separation tests were carried out in order to provide high yields (> 90% for Sn, > 85% for In), low total procedural blanks (~ 1 ng for Sn, < 3 pg for In) and low analytical uncertainties for the elements of interest in a variety of silicate sample matrices. Replicate analyses (n = 2–13) of Sn–In mass fractions gave combined measurement uncertainties (2u) that were generally < 3% and in agreement with literature data, where available. We present the first high‐precision In data for reference materials OKUM (32.1 ± 1.5 ng g^?1), DTS‐2b (2.03 ± 0.25 ng g^?1), MUH‐1 (6.44 ± 0.30 ng g^?1) and PCC‐1 (3.55 ± 0.35 ng g^?1) as well as the first Sn data for MUH‐1 (0.057 ± 0.010 μg g^?1) and DTS‐2b (0.623 ± 0.018 μg g^?1).  相似文献   

应用改进的ICP算法检测工业封头表面变形     

王春林  郑德华  孟敏  谢波 《测绘与空间地理信息》2015,(1):209-211

由于工业封头变形使得采集到的两期点云重心不一致,受点云重心变化的干扰,传统ICP算法出现局部收敛的情况,本文提出了一种基于点对间欧氏距离计算点云加权重心的ICP改进算法。该方法通过给不同距离的点对赋予权值,变形区域的点对距离较大,赋予的权值相对小,有效地消除了变形区域的点云对重心位置的影响。实验结果表明,该方法大大提高了ICP算法的精准性,有效消除重心变化的影响,从而可以准确地检测出工业封头变形区域。  相似文献   

大巴山南部房县东河辉绿玢岩LA ICP MS 锆石U Pb测年及其构造意义     

曹亮  张权绪  胡尚军  段其发  周云  于玉帅  邹先武  甘金木 《地质学报》2015,89(12):2314-2322

大巴山构造带位于秦岭造山带和扬子板块的过渡部位,形成于印支-燕山期,定型于喜山期。前人对北大巴山地区基性岩年代学已有研究,但对大巴山南部地区基性岩却很少高精度年龄报道。本文对大巴山南部房县东河地区的辉绿玢岩脉进行LA-ICP-MS锆石U-Pb年龄测定,结果表明,东河辉绿玢岩形成于439.3Ma,相当于早志留世。与北大巴山镇坪地区辉绿岩,紫阳-岚皋地区基性岩及火山岩形成时代基本一致。结合前人的研究结果表明,大巴山南部地区在早志留世处于张裂状态,东河地区的基性岩为岩石圈处于拉张状态下大陆裂谷作用产物。此处439.3Ma的年龄值,也说明此时扬子板块北缘普遍处于拉张的构造环境,代表了在早志留世大巴山南部裂谷盆地的伸展裂陷幅度达到最大。本次研究所获得的年龄数据,确定了围岩竹山组形成不晚于早志留世,限定地层时代为寒武纪-奥陶纪。  相似文献   

赣南横市地区基性岩墙的LA-ICP-MS锆石U-Pb年龄、地球化学特征及其地质意义   总被引：1，自引：0，他引：1  

左祖发  罗春林  王会敏  刘邦秀  刘春根  徐喆 《地质论评》2015,61(6):1417-1428

本文对江西赣南横市地区基性岩墙进行了年代学、岩石学和地球化学研究,主量元素特征和微量元素分析结果显示,基性岩墙为拉斑玄武岩系列和钙碱性系列,属于富钠基性岩类;Ti O2含量较高,平均含量1%,属于钛较高的基性岩类;A/NCK均小于1,属于准铝质基性岩类,具幔源型岩浆特征。基性岩墙LA-ICP-MS锆石U-Pb定年法测年结果为422.8±1.8 Ma和421.7±2.2 Ma,时代属于晚志留世,表明该基性岩墙是加里东期褶皱造山运动期后拉张(伸展)作用的产物。该地区不仅出露了加里东期同造山期和后造山期两类酸性花岗岩岩体,而且在该地区还同时出现加里东期的酸性岩类及基性岩类,大致反映了该地区从挤压型酸性岩浆侵位逐渐转换为拉张环境的基性岩浆侵位构造过程。  相似文献   

Methodology and Application of Hafnium Isotopes in Ilmenite and Rutile by MC‐ICP‐MS     

Caroline‐Emmanuelle Morisset  James S. Scoates  Dominique Weis  André Rahier 《Geostandards and Geoanalytical Research》2014,38(2):159-176

The high abundances of the high field‐strength elements in ilmenite and rutile make these minerals particularly suitable for hafnium isotopic investigations. We present a technique for separating Hf by ion exchange chemistry from high‐TiO₂ (> 40% m/m) minerals to achieve precise Hf isotopic composition analyses by MC (multiple collector)‐ICP‐MS. Following digestion and conversion to chlorides, the first elution column is used to separate iron and the rare earth elements, the second column is designed to separate most of the titanium from Hf, an evaporation step using HClO₄ is then performed to remove any trace of HF in preparation for the third column, which is needed to eliminate any remaining trace of titanium. The modified chemistry helped to improve the yields from < 10 to > 78% as well as the analytical precision of the processed samples (e.g., sample 2033‐A1, ¹⁷⁶Hf/¹⁷⁷Hf = 0.282251 ± 25 before vs. 0.282225 ± 6 after). The technique was tested on a case study in which the Hf isotopic ratios of ilmenite and rutile (analysed prior to the chemistry improvement) were determined and permitted to evaluate that the origin of rutile‐bearing ilmenite deposits is from the same or similar magma than their, respectively, associated Proterozoic anorthosite massifs (Saint‐Urbain and Lac Allard) of the Grenville Province in Québec, Canada.  相似文献   

Dating Micrometre‐Thin Rims Using a LA‐ICP‐MS Depth Profiling Technique on Zircon from an Archaean Metasediment: Comparison with the SIMS Depth Profiling Method     

Colter J. Kelly  Christopher R.M. McFarlane  David A. Schneider  Simon E. Jackson 《Geostandards and Geoanalytical Research》2014,38(4):389-407

Laser ablation‐inductively coupled plasma‐mass spectrometry (LA‐ICP‐MS) was examined as a tool for measuring isotopic variation as a function of ablation depth in unpolished zircon from an Archaean metasediment specimen. This technique was able to identify micrometre‐thin (> 3 μm) isotopically distinct mineral domains characterised by ca. 100 Myr younger ²⁰⁷Pb/²⁰⁶Pb ages associated with 2s age uncertainties as low ~ 0.2%, as well as elevated U content relative to grain interiors (up to an order of magnitude). Our calculated drilling rate suggests that each laser pulse excavated depths of ~ 0.06 μm. Ages resolved through the LA‐ICP‐MS methods overlap the 2s uncertainties of ²⁰⁷Pb/²⁰⁶Pb ages measured using SIMS depth profiling on the same zircon population. The rims were further evinced by the detection of relative enrichment (> 3 orders of magnitude) in REE in the outermost micrometres of the same zircon, measured using a different and independent LA‐ICP‐MS depth profiling technique. We propose a LA‐ICP‐MS U–Pb technique capable of quickly identifying and quantifying rims, which are indication of late, yet geologically significant, fluid events that are otherwise undefined.  相似文献   

Apatite Chlorine Concentration Measurements by LA‐ICP‐MS     

David M. Chew  Ray A. Donelick  Margaret B. Donelick  Balz S. Kamber  Michael J. Stock 《Geostandards and Geoanalytical Research》2014,38(1):23-35

Apatite incorporates variable and significant amounts of halogens (mainly F and Cl) in its crystal structure, which can be used to determine the initial F and Cl concentrations of magmas. The amount of chlorine in the apatite lattice also exerts an important compositional control on the degree of fission‐track annealing. Chlorine measurements in apatite have conventionally required electron probe microanalysis (EPMA). Laser ablation inductively coupled plasma‐mass spectrometry (LA‐ICP‐MS) is increasingly used in apatite fission‐track dating to determine U concentrations and also in simultaneous U‐Pb dating and trace element measurements of apatite. Apatite Cl measurements by ICP‐MS would remove the need for EPMA but the high (12.97 eV) first ionisation potential makes analysis challenging. Apatite Cl data were acquired using two analytical set‐ups: a Resonetics M‐50 193 nm ArF Excimer laser coupled to an Agilent 7700× quadrupole ICP‐MS (using a 26 μm spot with an 8 Hz repetition rate) and a Photon Machines Analyte Excite 193 nm ArF Excimer laser coupled to a Thermo Scientific iCAP Qc (using a 30 μm spot with a 4 Hz repetition rate). Chlorine concentrations were determined by LA‐ICP‐MS (1140 analyses in total) for nineteen apatite occurrences, and there is a comprehensive EPMA Cl and F data set for 13 of the apatite samples. The apatite sample suite includes different compositions representative of the range likely to be encountered in natural apatites, along with extreme variants including two end‐member chlorapatites. Between twenty‐six and thirty‐nine isotopes were determined in each apatite sample corresponding to a typical analytical protocol for integrated apatite fission track (U and Cl contents) and U‐Pb dating, along with REE and trace element measurements. ³⁵Cl backgrounds (present mainly in the argon gas) were ~ 45–65 kcps in the first set‐up and ~ 4 kcps in the second set‐up. ³⁵Cl background‐corrected signals ranged from ~ 0 cps in end‐member fluorapatite to up to ~ 90 kcps in end‐member chlorapatite. Use of a collision cell in both analytical set‐ups decreased the low mass sensitivity by approximately an order of magnitude without improving the ³⁵Cl signal‐to‐background ratio. A minor Ca isotope was used as the internal standard to correct for drift in instrument sensitivity and variations in ablation volume during sessions. The ³⁵Cl/⁴³Ca values for each apatite (10–20 analyses each) when plotted against the EPMA Cl concentrations yield excellently constrained calibration relationships, demonstrating the suitability of the analytical protocol and that routine apatite Cl measurements by ICP‐MS are achievable.  相似文献   

Measurement of the Isotopic Composition of Molybdenum in Geological Samples by MC‐ICP‐MS using a Novel Chromatographic Extraction Technique     

Jie Li  Xi‐Rong Liang  Li‐Feng Zhong  Xuan‐Ce Wang  Zhong‐Yuan Ren  Sheng‐Ling Sun  Zhao‐Feng Zhang  Ji‐Feng Xu 《Geostandards and Geoanalytical Research》2014,38(3):345-354

A novel preconcentration method is presented for the determination of Mo isotope ratios by multi‐collector inductively coupled plasma‐mass spectrometry (MC‐ICP‐MS) in geological samples. The method is based on the separation of Mo by extraction chromatography using N‐benzoyl‐N‐phenylhydroxylamine (BPHA) supported on a microporous acrylic ester polymeric resin (Amberlite CG‐71). By optimising the procedure, Mo could be simply and effectively separated from virtually all matrix elements with a single pass through a small volume of BPHA resin (0.5 ml). This technique for separation and enrichment of Mo is characterised by high selectivity, column efficiency and recovery (~ 100%), and low total procedural blank (~ 0.18 ng). A ¹⁰⁰Mo‐⁹⁷Mo double spike was mixed with samples before digestion and column separation, which enabled natural mass‐dependent isotopic fractionation to be determined with a measurement reproducibility of  < 0.09‰ (δ^98/95Mo, 2s) by MC‐ICP‐MS. The mean δ^98/95Mo_{SRM 3134} (NIST SRM 3134 Mo reference material; Lot No. 891307) composition of the IAPSO seawater reference material measured in this study was 2.00 ± 0.03‰ (2s, n = 3), which is consistent with previously published values. The described procedure facilitated efficient and rapid Mo isotopic determination in various types of geological samples.  相似文献