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1.
This paper evaluates the analytical precision, accuracy and long‐term reliability of the U‐Pb age data obtained using inductively coupled plasma–mass spectrometry (ICP‐MS) with a frequency quintupled Nd‐YAG (λ = 213nm) laser ablation system. The U‐Pb age data for seven standard zircons of various ages, from 28 Ma to 2400 Ma (FCT, SL13, 91500, AS3, FC1, QGNG and PMA7) were obtained with an ablation pit size of 30 μm diameter. For 207Pb/206Pb ratio measurement, the mean isotopic ratio obtained on National Institute of Standards and Technology (NIST) SRM610 over 4 months was 0.9105 ± 0.0014 (n = 280, 95% confidence), which agrees well with the published value of 0.9096. The time‐profile of Pb/U ratios during single spot ablation showed no significant difference in shape from NIST SRM610 and 91500 zircon standards. These results encouraged the use of the glass standard as a calibration standard for the Pb/U ratio determination for zircons with shorter wavelength (λ = 213 nm) laser ablation. But 206Pb/238U and 207Pb/235U ages obtained by this method for seven zircon standards are systematically younger than the published U‐Pb ages obtained by both isotope dilution–thermal ionization mass spectrometry (ID‐TIMS) and sensitive high‐resolution ion‐microprobe (SHRIMP). Greater discrepancies (3–4% younger ages) were found for the 206Pb/238U ages for SL13, AS3 and 91500 zircons. The origin of the differences could be heterogeneity in Pb/U ratio on SRM610 between the different disks, but a matrix effect accuracy either in the ICP ion source or in the ablation‐transport processes of the sample aerosols cannot be neglected. When the 206Pb/238U (= 0.2302) newly defined in the present study is used, the measured 206Pb/238U and 207Pb/235U ages for the seven zircon standards are in good agreement with those from ID‐TIMS and SHRIMP within ±2%. This suggests that SRM610 glass standard is suitable for ICP‐MS with laser ablation sampling (LA‐ICP‐MS) zircon analysis, but it is necessary to determine the correction factor for 206Pb/238U by measuring several zircon standards in individual laboratories.  相似文献   

2.
Laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) is used to compare the suitability of four cassiterite (SnO2) materials (SPG, Yankee, AY-4 and Jian-1), and three matrix-mismatched reference materials (NIST SRM 612, NIST SRM 614 and 91500 zircon) for normalisation of U-Pb and Pb-Pb isotope ratios in cassiterite. The excess variance of ages determined by LA-ICP-MS is estimated to be ±0.33% for 207Pb/206Pb vs. 208Pb/206Pb isochron ages and ± 1.8% and for U-Pb ages. Incorporation of this excess variance in cassiterite ages is necessary for realistic uncertainties. 207Pb-206Pb ages are advantageous for dating Precambrian cassiterite such as SPG compared with U-Pb ages as matrix effect on instrumental mass fractionation of Pb isotopes are generally considered to be minor. We note minor bias in 207Pb/206Pb vs. 208Pb/206Pb isochron ages (~ 0.6%) when using either the NIST SRM 614 or 91500 zircon reference materials and emphasise the requirement for uncertainty propagation of all sources of error and reference materials with comparable U and Pb mass fraction to the cassiterite. The 238U/206Pb isotopic ratios from normalisation to matrix-mismatched reference materials show varied results, which emphasises the need to use matrix-matched reference materials for calculating U-Pb ages. When cross-calibrated against each other, LA-ICP-MS U-Pb ages of the ca. 1535 Ma SPG, ca. 245 Ma Yankee and ca. 155 Ma Jian-1 cassiterites are all consistent with their ID-TIMS values.  相似文献   

3.
High precision isotope ratio and trace element determination can be achieved with modern quadrupole ICP-MS provided that short and long-term instrument performance is accurately monitored. Here we present results for the isotope ratios 6Li/7Li, 147Sm/149Sm, 160Dy/161Dy, 207Pb/206Pb, 208Pb/206Pb, 206Pb/204Pb and 235U/238U with which we determined long-term isotope ratio stability of relevance to both trace element and isotope determination. With respect to trace element determination, we first present long-term observations regarding oxide formation rates of Ba and Nd on light REE and heavy REE, as well as Zr on Ag. These showed good correlations and could be used to correct effectively the interference. The efficacy of this correction was demonstrated with analyses of the rock reference material BHVO-2 at both low and high oxide formation rates. Next, we studied the long-term reproducibility of a Dy isotope ratio that was measured to correct for the isobaric interference on Gd. It was found that, regardless of tuning condition, the ratio reproduced very well (0.58% RSD, 1s) and that the estimate of the Gd concentration did not suffer from the large correction (> 10%) caused by the Dy isobar. Long-term reproducibilities of Li, Sm and U isotope ratios, required for accurate mass bias correction when isotopically enriched internal standards of these elements are employed, were measured in the rock reference materials AGV-2 and JA-3 over a time period of up to 3 years. As expected, the Li isotope ratio showed the largest variability (RSD = 7%), but the other two ratios had relative external reproducibilities of only 1.01% (1s, U) and 0.67% (Sm). The mass bias-induced scatter in measurements for Sm and U was so small that the internal standard correction was effective, even for samples with high concentrations of these elements. With regard to Pb-isotope ratio determination, we also present long-term reproducibility for NIST SRM 982, run as an unknown and two accuracy tests for Pb separated from granitoids and from meteorites. It is demonstrated that the obtained ratios, including those involving 204Pb, are accurate relative to MC-ICP-MS determinations and of comparable precision to conventional TIMS analysis. The excellent agreement between all data sets shows the potential of modern quadrupole ICP-MS instrumentation for Pb-isotope determination, particularly for samples with very low Pb content.  相似文献   

4.
The development of the MC-ICP-MS method, which was launched about one decade ago and was largely stimulated by the need to solve geological problems, has opened a new avenue in isotope mass spectrometry. One of the advantages of this method is the possibility of applying a newly developed approach to the correction of analytical results for the effect of mass discrimination by normalizing the measured isotope ratios of an element to a reference (standard) isotope ratio of another element. This makes it possible to overcome the main disadvantage of conventional thermal ionization mass spectrometry (TIMS), in which the effect of mass discrimination cannot be fully taken into account during isotope analysis, and thus to implement a highly accurate method for the analysis of Pb-isotope composition. In application to the capability of the NEPTUNE MC-ICP mass spectrometer, we optimized and calibrated a method for high-accuracy Pb isotope analysis in solutions spiked with Tl, with all currently measured Pb-isotope ratios normalized to the standard 205Tl/203Tl ratio (TLN-MC-ICP-MS). The factors affecting the random and systematic analytical errors were examined, and the optimal operating regime and analytical conditions were determined. Much attention was paid to the correlation of the measurement results and the mass discrimination effect determined from the 205Tl/203Tl ratio. The value of the 205Tl/203Tl normalizing ratio was analytically determined through isotope analyses of the NIST SRM 981, and SRM 982 standard samples of Pb-isotope composition. The data obtained for two mixtures Tl + Pb (SRM 982) and Tl + Pb (SRM 981) in ten replicate analyses were 2.38898 ± 12 and 2.38883 ± 20, respectively. These results are in good mutual agreement, and their general mean 205Tl/203Tl = 2.3889 ± 1 coincides (within the error) with the recently published values of 2.3887 ± 7 [Collerson et al., 2002] and 2.3889 ± 1 [Thirlwall, 2002]. The precision of the method (±2SD), which was assayed by the long-term reproducibility of the results of replicate analyses of SRM 981 and seven galena samples (90 analyses) was 0.016–0.018% for the 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb ratios and 0.005 and 0.009% for the 207Pb/206Pb and 208Pb/206Pb ratios, respectively. The precision of the isotope analysis of common Pb was significantly improved (by factors of 6–10 for various isotope ratios) compared with the precision of TIMS techniques acceptable in isotope studies during three decades. The described method was applied to examine the Pb-isotope composition of approximately 250 samples of galena, scheelite, and pyrite from a number of well known (including large) gold, sulfied, and base-metal deposits. The precision of the method (0.01–0.02%) makes it possible to study small inter-and intra-phase differences in Pb-isotope ratios in hydrothermal and magmatic rocks, to assay the scale of regional and variations in the isotope composition of ore Pb, and to correlate the Pb-isotope composition of rocks and ores and reveal its evolutionary trends.  相似文献   

5.
采用装配多离子计数器系统的TRITON Plus热电离质谱仪（thermal ionization mass spectrometer,TIMS）,建立了多离子计数器动态多接收锆石Pb同位素（以205Pb为稀释剂）测定方法.相对多离子计数器静态多接收方法,该方法完全消除了不同离子计数器间增益差异对锆石Pb同位素测定的影响.相对传统的单个二次电子倍增器（secondary electron multiplier,SEM）五次跳峰的锆石Pb同位素测定方法,该方法两次跳峰即可测定全部Pb同位素比值,Pb同位素离子流接收效率提高2.5倍,同时,降低了离子流稳定性对Pb同位素分析结果的影响.为验证方法的可靠性,对加入205Pb稀释剂的NIST981 Pb标准和标准锆石清湖（Qinghu）进行了测定.对5×10-11 g 205Pb-NIST981 Pb混标,207Pb/206Pb测定精度达到0.079%（2RSD,n=20）;对清湖标准锆石,获得的年龄结果为159.51±0.11 Ma（2SE,n=7;MSWD=1.1）,与文献报道值在误差范围内一致.   相似文献   

6.
锆石U-Pb年代学方法已经成为地质学研究必不可少的方法。本文收集整理了二十世纪八十年代以来分散在期刊论文、学位论文等多种出版载体中的锆石U-Pb年代学数据,建成中国大陆单颗粒锆石数据库中文子库。该数据子库涉及截至到2017年底的文献2331篇,有效数据154768条目,数据总量已经能够用来进行数据的初步分析和相关地球科学研究。数据子库中年龄-年龄绝对误差关系的分析表明,Age(~(206)Pb/~(238)U)、Age(~(207)Pb/~(235)U)、Age(~(207)Pb/~(206)Pb)在不同的地质年代区间误差表现有所不同。在小于1684.4Ma、1684.4~2855.2Ma、大于2855.2Ma年龄区Age(~(206)Pb/~(238)U)、Age(~(207)Pb/~(235)U)、Age(~(207)Pb/~(206)Pb)的误差最小、置信度最好,除了Age(~(207)Pb/~(235)U)测试方法的原因外,Age(~(206)Pb/~(238)U)和Age(~(207)Pb/~(206)Pb)可分别作为不同年龄段的推荐年龄。将选用的推荐年龄运用于LA-ICP-MS、SHRIMP、SIMS三种方法的比较,得出其适用于不同地质年代的范围。推荐年龄运用于年龄-频数图中并使用高斯多峰拟合,则可发现中国大陆锆石存在6个生长峰期,分别为131.71Ma、255.17Ma、442.42Ma、811.56Ma、1868.36Ma和2505.31Ma等;更小尺度下的新生代则存在七个峰期,分别为16.99Ma、27.64Ma、35.26Ma、43.44Ma、48.27Ma、52.74Ma和62.07Ma等,峰期及其对应测试点的位置可与中国大陆地壳演化重大历史事件对应。  相似文献   

7.
The results of geochronological studies on columbite-tantalite and monazite from the rare metal pegmatites of the Kawadgaon–Challanpara area in Bastar craton, central India are presented. Columbite-tantalite yielded U-Pb concordia upper intercept age of 1978±16 Ma (MSWD = 0.18). Radiogenic 207Pb*/206Pb* (T7/6) ages on 4 out of 5 columbite-tantalite vary in a narrow range of 1903 to 2077 Ma and are similar to U-Pb age, whereas, one sample shows younger 207Pb*/206Pb*(T7/6) age of 1728 Ma. Younger Pb-Pb age of 1744 ± 250 Ma (MSWD = 150) has also been indicated by these columbite-tantalite samples. Four out of five monazite samples define Pb-Pb errorchron age of 2050±370 Ma (MSWD = 165) and radiogenic 207Pb*/206Pb* (T7/6) ages on 3 out of 5 monazites show a narrow range of 1983 to 2083 Ma. Other two samples show younger 207Pb*/206Pb*(T7/6) ages as 1254 Ma and 1592Ma. Both monazite and columbite-tantalite indicate disturbance in Pb and U isotopic systematics as revealed by high MSWD. However, selected samples from both monazite and columbite-tantalite indicate age of their formation as c. 2000 Ma. Younger ages, i.e., 1254 to 1744 Ma are indicative of later geological disturbances. Reported age of c. 2000 Ma is comparable to Rb-Sr date of pegmatitic muscovite (1850-2330 Ma) from this area and is younger to intrusive granites of c. 2500 Ma. By analogy, therefore, it may be inferred that the age of the rare element mineralization may be ~2000 Ma old, and linked with younger granitic activity that spanned over the period from 2300 to 2100 Ma in the Bastar craton.  相似文献   

8.
Gem quality andradite-rich garnet (IUC-1), obtained from the Miocene trachyte dome near Ankara city (Turkey), has been identified as a potential natural secondary reference material for U-Pb dating. In this study, U-Pb dating was performed in five different laboratories using isotope dilution TIMS and laser ablation ICP-MS to determine the homogeneity of euhedral garnet crystals. The U-Pb ID-TIMS data for IUC-1 yielded 207Pb/235U and 206Pb/238U ages of 20.9 ± 0.4 and 20.6 ± 0.8 Ma respectively, and these values are consistent with U-Pb LA-ICP-MS analyses, in which different garnet crystals yielded ages of 20.8 ± 0.1, 20.7 ± 0.1, 20.7 ± 0.2 and 20.2 ± 0.1 Ma. An andradite (IUC-2) from the Serçeören wollastonite skarn (Turkey) can be used as a secondary reference material provided detailed imaging of the crystals is undertaken. ID-TIMS data yielded 207Pb/235U and 206Pb/238U ages of 20.4 ± 0.4 and 20.9 ± 1.0 Ma respectively, and yielded U-Pb ages on different grains of 20.5 ± 0.1, 20.7 ± 1.0, 20.8 ± 1.7 and 20.9 ± 1.6 Ma. The assigned weighted mean age of IUC-1 (20.4 ± 0.5 Ma, 2s) is proposed as a 2023 reference value. IUC-1 garnet is expected to contribute significantly to rapidly developing garnet geochronology in the near future.  相似文献   

9.
Inductively coupled plasma mass spectrometry (ICP-MS) has been used to measure the concentration and isotopic composition of Pb in archaeological human and animal skeletal remains, soil from a village site of the Omaha tribe (U.S.A.) and cosmetic pigments.Lead concentrations in human bones from the Omaha tribe vary between 4.8 and 2570 μg/g, with younger people having the highest concentrations. Lead concentrations in animal bones from an Omaha village vary between 0.6 and 3.7 μg/g, and those of three soil samples range between 18 and 21 μg/g. Lead concentrations found in human bones from Anasazi (Utah, U.S.A.) and Alta (Peru) populations vary between 0.7 and 3.2 μg/g.Isotope ratios of a reagent grade Pb(NO3)2 solutions were measured by thermal ionization mass spectrometry (TIMS), as well as by ICP-MS to provide laboratory reference materials. The accuracy of the ICP-MS measurements relative to TIMS for the standard solution were found to be within 0.02–0.31% for206Pb/204Pb, 0.02–0.55% for207Pb/204Pb, and 0.16–0.56% for208Pb/204Pb. The precision of measurements on artifacts was 0.42–0.65% for206Pb/204Pb and 0.41–0.62% for207Pb/204Pb, whereas the precision for the same ratios for the bones was 0.85–1.8 and 0.82–1.67%, respectively. For the cosmetic lead-bearing pigments, a precision of 0.07–0.15% was found for both206Pb/204Pb and207Pb/204Pb ratios. Lead isotope ratios of artifacts give a radiogenic Pb signature, of which are close to signatures from PbZn mines of the central U.S. region. Lead isotope ratios of the pigments give non-radiogenic Pb signatures. Lead isotope ratios of the bones differ from those of the artifacts, and although similar in isotopic ratio to the pigments, they are more scattered, suggesting potential mixing of Pb from different regions.  相似文献   

10.
道伦达坝矿床位于大兴安岭南段,是一个铜钨锡矿床,其铜、钨、锡储量均达中型。矿体呈脉状,主要产于二叠系砂板岩中的断裂破碎带中,华力西期黑云母花岗岩中的断裂破碎带中亦赋存有矿体。文章选取2件石英-萤石-白云母-电气石-锡石-黑钨矿阶段的矿石样品对其中的进行了LA-ICP-MS U-Pb定年,获得2件样品的~(207)Pb/~(206)Pb-~(238)U/~(206)Pb谐和年龄分别为(134.7±6.6)Ma(MSWD=1.4)和(136.8±7.4)Ma(MSWD=1.7),~(206)Pb/~(207)Pb-~(238)U/~(207)Pb等时线年龄分别为(132±12)Ma(MSWD=0.76)和(135±13)Ma(MSWD=0.9)。锡石定年结果表明,道伦达坝矿床形成于早白垩世。对矿区外围张家营子岩体中的斑状细粒花岗岩进行了LA-ICP-MS锆石U-Pb测年,获得的~(206)Pb/~(238)U加权平均年龄为(135±1)Ma(MSWD=1.3),该岩体的形成年龄与道伦达坝矿床的成矿年龄在误差范围内一致。本次定年结果表明道伦达坝矿床形成于早白垩世,与同期的花岗质岩浆活动有密切的成因联系,该矿床属于与花岗岩有关的岩浆热液脉型矿床。  相似文献   

11.
We present the results of a comparative study of several geochronometer minerals (baddeleyite, zircon, apatite, phlogopite and tetraferriphlogopite) and isotopic systems (U-Pb, Th-Pb and Rb-Sr) from phoscorites (magnetite-forsterite-apatite-calcite rocks) and carbonatites of the Kovdor ultramafic-alkaline-carbonatite massif, Kola Peninsula, Russia. Uranium, thorium and their decay products are extremely fractionated by minerals that crystallise from carbonatite and phoscorite magma. We obtain high-precision ages from different chronometers, compare their accuracy, and evaluate the role of geochronological pitfalls of initial radioactive disequilibrium, differential migration of radiogenic isotopes, and inaccurate decay constants.Apatite yielded concordant U-Th-Pb ages between 376 and 380 Ma. The accuracy of the apatite 238U-206Pb ages is, however, compromised by uncertainty in the amount of radiogenic 206Pb produced from initial excess 230Th. The 235U-207Pb ages are relatively imprecise due to large common Pb correction and the uncertainty in the initial Pb isotopic composition. The Th-Pb system yields a more precise age of 376.4 ± 0.6 Ma.Zircon from two carbonatite samples is characterised by moderate to low U contents, high Th contents, and very high Th/U ratios up to 9000. The 206Pb*/238U systems in the zircon are strongly affected by the presence of excess 206Pb*, produced by decay of initial 230Th. The 208Pb*/232Th ages of zircon from both carbonatite samples are uniform and yield a weighted average of 377.52 ± 0.94 Ma.Baddeleyite U-Pb analyses are 3 to 6% normally discordant and have variable 207Pb*/206Pb* apparent ages. Eleven alteration-free baddeleyite fractions from three samples with no evidence for Pb loss yield uniform 206Pb*/238U ages with a weighted average of 378.54±0.23 Ma (378.64 Ma after correction for initial 230Th deficiency), which we consider the best estimate for age of the phoscorite-carbonatite body of the Kovdor massif. The 206Pb*/238U ages of baddeleyite fractions from five other samples spread between 378.5 and 373 Ma, indicating a variable lead loss up to 1.5%. The anomalously old 207Pb/235U and 207Pb/206Pb ages are consistent with the presence of excess radiogenic 207Pb* in the baddeleyite. We interpret this as a result of preferential partitioning of 231Pa to baddeleyite.Fifteen phlogopite and tetraferriphlogopite fractions from five carbonatite and phoscorite samples yielded precise Rb-Sr isochron age of 372.2 ± 1.5 Ma, which is 5 to 7 m.y. younger than our best estimate based on U-Th-Pb age values. This difference is unlikely to be a result of the disturbance or late closure of Rb-Sr system in phlogopite, but rather suggests that the accepted decay constant of 87Rb is too high.Comparative study of multiple geochronometer minerals from the Kovdor massif has revealed an exceptional complexity of isotopic systems. Reliable ages can be understood through systematic analysis of possible sources of distortion. No single geochronometer is sufficiently reliable in these rocks. Th-Pb and Rb-Sr can be a very useful supplement to U-Pb geochronometry, but the routine use of these geochronometers together will require more precise and accurate determination of decay constants for 232Th and 87Rb.  相似文献   

12.
1 Introduction According to recent researches, the North China Craton consists of three parts: the eastern block, western block and central zone (Zhao, 2001; Wilde et al., 2002). Paleoarchean continental blocks and zircon residuals have only been found in a few regions, such as Anshan, East Liaoning (Liu et al., 1992; Song et al., 1996; Wan et al., 2002, 2005), Caozhuang, East Hebei (Liu et al., 1992) and Xinyang, West Henan (Zheng et al., 2004), which are mainly distributed in the east…  相似文献   

13.
Tin mineralisation is closely related to rhyolite stocks and dykes which occur in the endo- and exocontact of the Eibenstock granite, Erzgebirge, Germany. The same structures which cut the granite control the rhyolite emplacement and the location of ore-bearing greisen bodies. Albitisation and greisenisation related to tin mineralisation as well as sericitisation and argillic alteration may be traced by changes in chemical and mineralogical composition of both rhyolite and granite wall rock. Comprehensive zircon studies by scanning electron microscopy (secondary and backscattered electron as well as cathodoluminescence imaging; EDX measurements) reveal that zircon from rhyolite and from the enclosing granite shows significant changes in chemical composition and crystallinity, including distortion of the U-Pb isotope system when affected by greisenisation. Single evaporation analysis of zircon from rhyolite with little or no greisenisation gave a 207Pb/206Pb age of 290±5 Ma, whereas zircon from little altered granite gave a 207Pb/206Pb age of 320±8 Ma. The single evaporation age of zircon from rhyolite is confirmed by 238U/206Pb SHRIMP ages of 297±8 Ma. The significant time gap of at least 20 Ma between granite intrusion and rhyolite formation suggests that the late magmatic evolution of the Eibenstock granite cannot be regarded as a source for tin-ore forming fluids as previously assumed.  相似文献   

14.
We have developed new analytical procedures to measure precise and accurate 238U–206Pb and 235U–207Pb ages for young (~ 1 Ma) zircons using laser ablation‐ICP‐mass spectrometry. For young zircons, both careful correction for the background counts and analysis of very small Pb/U ratios (i.e., 206Pb/238U < 0.00016 and 207Pb/235U < 0.0001 for 1 Ma zircons) are highly desired. For the correction of the background, the contribution of the background signal intensities for the analytes, especially for the residual signal intensities for 206Pb and 207Pb, was defined through laser ablation of synthesised zircons (ablation blank) containing negligible Pb. The measured signal intensities for 202Hg, 206Pb and 207Pb signals obtained by the ablation blank were slightly higher than those obtained by data acquisition without laser ablation (gas blank). For the wider dynamic range measurements on Pb/U ratios, an attenuator device for the ion detection system was employed to extend the capability to monitor high‐intensity signals (i.e., > 3 Mcps). Through the attenuator device, the ion currents were reduced to 1/450 of the signal intensity without the attenuator. Because the switching time for the attenuator was shorter than 1 ms, signal intensities for only specific isotopes could be reduced. With attenuation of the 238U signal, counting statistics on 206Pb and 207Pb isotopes could be improved and counting loss on the 238U signal could be minimised. To demonstrate the reliability of this new analytical technique, 238U–206Pb and 235U–207Pb ages for three young zircon samples (collected from Osaka Group Pink Volcanic Ash, Kirigamine and Bishop Tuff) were measured. The data presented here demonstrate clearly that the present technique could become a major analytical tool for in situ U–Pb age determination of young zircons (~ 1 Ma).  相似文献   

15.
The Bayan Obo deposit in North China contains the largest rare-earth element (REE) resources in the world, but its forming time remains controversial. Nearly one hundred carbonatite dykes occur around the Bayan Obo deposit, including dolomite, calcite and calcite–dolomite carbonatite varieties. Zircons from a REE-rich carbonatite dyke and wallrock quartz conglomerate at Bayan Obo have been analyzed for U–Pb to determine the age of the dyke. Zircon from the carbonatite dyke, analyzed by conventional isotope dilution thermal ionization mass spectrometry (ID-TIMS), yielded an upper intercept age of 1417 ± 19 Ma. This age is confirmed by SHRIMP U–Pb analysis of zircon from the same carbonatite dyke, which gave a 207Pb/206Pb weighted mean age of 1418 ± 29 Ma. In situ Nd isotope measurements of monazite collected from the carbonatite dyke gave an isochron age of 1275 ± 87 Ma. These results demonstrate that the dyke intruded ~ 1400 Ma. In view of predecessor's results, it is clarified that the REE mineralization at Bayan Obo occurred at ca. 1400 Ma, consistent with the timing of carbonatite dyke intrusion in the region. The youngest detrital zircons from the quartz conglomerate yielded a 207Pb/206Pb weighted mean age of 1941 ± 7 Ma using LA ICP-MS U–Pb method. Detrital zircons in the carbonatite dyke also gave a mean apparent age of 1932 ± 3 Ma using ID-TIMS U–Pb method and 1914 ± 14 Ma using SHRIMP U–Pb method. These ages constrain the beginning active time of the Zha'ertai–Bayan Obo rift in the northern margin of the North China Craton after ~ 1900 Ma.  相似文献   

16.
Lead isotope amount ratios are commonly used in diverse fields such as archaeometry, geochemistry and forensic science. Currently, five reference materials with certified lead isotope amount ratios are available, namely NIST SRM 981, 982 and 983, GBW‐04442 and NMIJ 3681‐a. Only NIST SRM 981 and NMIJ 3681‐a have approximately natural isotopic compositions, and NIST SRM 981 is predominantly used for correcting mass discrimination/mass fractionation in the applied mass spectrometric procedures. Consequently, there is no other certified reference material available to be used for validation and/or quality control of the analytical procedures applied to lead isotope amount ratio measurements. To fill this gap, two new reference materials have been produced and certified for their lead isotope amount ratios. For both certified reference materials, complete uncertainty budgets have been calculated and SI traceability has been established. This provides the users with independent means for validating and verifying their analytical procedures and for conducting quality control measures. ERM‐EB400 is a bronze material with a nominal lead mass fraction of 45 mg kg?1 and certified lead isotope amount ratios of n(206Pb)/n(204Pb) = 18.072(17) mol mol?1, n(207Pb)/n(204Pb) = 15.578(18) mol mol?1 and n(208Pb)/n(204Pb) = 38.075(46) mol mol?1 with the associated expanded uncertainties (k = 2) given in brackets. ERM‐AE142 is a high‐purity solution of lead in 2% nitric acid with a nominal mass fraction of 100 mg kg?1 and certified Pb isotope amount ratios of n(206Pb)/n(204Pb) = 21.114(17) mol mol?1, n(207Pb)/n(204Pb) = 15.944(17) mol mol?1 and n(208Pb)/n(204Pb) = 39.850(44) mol mol?1 with the associated expanded uncertainties (k = 2) given in brackets. Both materials are specifically designed to fall within the natural lead isotopic variation and to assist users with the validation and verification of their analytical procedures. Note that while one of these reference materials requires the chemical separation of Pb from its matrix (ERM‐EB400), the other does not (ERM‐AE142). As additional information, δ208/206PbNIST SRM981 values are provided for both materials. For ERM‐AE142, a delta value of δ208/206PbNIST SRM981 = ?28.21(30)‰ was obtained, and for ERM‐EB400, a delta value of δ208/206PbNIST SRM981= ?129.47(38)‰ was obtained, with the associated expanded uncertainties (k = 2) given in brackets.  相似文献   

17.
We report the first precise U–Pb isotope data on cassiterite from the large Xianghualing tin-polymetallic deposit in the central Nanling district, South China. The results show that four separates from sample XF-51 have a relatively narrow range of 206Pb/238U apparent ages, varying from 152 to 157 Ma, and the three 206Pb/238U apparent ages yield a weighted average value of 156 ± 4 Ma (MSWD = 0.32). Separates from two other cassiterite samples do not have sufficient radiogenic Pb to generate a reliable 206Pb/238U age. Seven separates from the above three cassiterite samples define a well-constrained 238U–206Pb isochron corresponding to an age of 157 ± 6 Ma (MSWD = 34). A comparison of the U–Pb cassiterite ages with published Ar–Ar dates on muscovite from this deposit and K–Ar age data on biotite from the pluton genetically related to the tin mineralization in this area demonstrates that the U–Pb isotope system of cassiterite is a potential geochronometer. Combined with the Ar–Ar dates of muscovite from this deposit, we can constrain the absolute age of tin-polymetallic mineralization in Xianghualing at 154–157 Ma. The dates obtained in this study, consistent with the published geochronological results from other important deposits in this region, reveal that the large-scale tungsten–tin mineralization in the central Nanling region was predominantly emplaced during 150–161 Ma.  相似文献   

18.
The Plutonic Well Greenstone Belt (PWGB) is located in the Marymia Inlier between the Yilgarn and Pilbara cratons in Western Australia, and hosts a series of major Au deposits. The main episode of Au mineralisation in the PWGB was previously interpreted to have either accompanied, or shortly followed, peak metamorphism in the late Archean at ca 2650 Ma with a later, minor, event associated with the Capricorn Orogeny. Here we present new Pb isotope model ages for sulfides and Rb–Sr ages for mica, as well as a new 207Pb–206Pb age for titanite for samples from the Plutonic Gold Mine (Plutonic) at the southern end of the PWGB. The majority of the sulfides record Proterozoic Pb isotope model ages (2300–2100 Ma), constraining a significant Au mineralising event at Plutonic that occurred >300 Myr later than previously thought. A Rb–Sr age of 2296 ± 99 Ma from muscovite in an Au-bearing sample records resetting or closure of the Rb–Sr system in muscovite at about the same time. A younger Rb–Sr age of 1779 ± 46 Ma from biotite from the same sample may record further cooling, or resetting during a late-stage episode of metasomatism in the PWGB. This could have been associated with the 1820–1770 Ma Capricorn Orogeny, or a late-stage hydrothermal event potentially constrained by a new 207Pb–206Pb age of 1725 ± 26 Ma for titanite in a chlorite–carbonate vein. This titanite age correlates with a pre-existing age for a metasomatic event dated at 1719 ± 14 Ma by U–Pb ages of zircon overgrowths in a sample from the Marymia Deposit. Based on the Pb-isotope data presented here, Au mineralising events in the PWGB are inferred to have occurred at ca 2630, 2300–2100 Ma, during the Glenburgh and Capricorn orogenies, and 1730–1660 Ma. The 2300–2100 Ma event, which appears to have been significant based on the amount of sulfide of this age, correlates with the inferred age for rifting of the Marymia Inlier from the northern margin of the Yilgarn Craton. The texturally-later visible Au may have been deposited during the Glenburgh and Capricorn orogenies.  相似文献   

19.
都龙锡锌多金属矿床LA-MC-ICPMS锡石U-Pb测年及其意义   总被引：12，自引：9，他引：3  
云南都龙锡锌多金属矿床是我国最大的锡石硫化物矿床之一。缺乏精确可靠的成矿年代学判据,是该矿床成因认识存在较大分歧的重要原因之一,严重制约了地质勘探工作的深入。本文应用LA-MC-ICP-MS微区原位U-Pb同位素测年技术,对都龙矿区曼家寨矿段的锡石样品进行了研究,获得DL12-716、DL12-722、DL12-740等三件样品的206Pb/207Pb-238U/207Pb等时线年龄分别为89.2±4.1Ma(N=22,MSWD=4.5)、88.0±1.6Ma(N=24,MSWD=2.3)和87.2±3.9Ma(N=31,MSWD=14),207Pb/206Pb-238U/206Pb谐和年龄分别为96.6±3.5Ma(MSWD=8.1)、93.6±1.6Ma(MSWD=5.8)和82.0±2.5Ma(MSWD=11)。结合矿床地质特征和前人成岩-成矿年代学成果,表明都龙矿区锡成矿作用主要发生在晚白垩纪,与燕山晚期岩浆热液活动关系密切,结合地质事实,表明燕山晚期岩浆热液活动是老君山矿集区锡钨多金属成矿的关键。通过区域地质及年代学对比,表明滇东南地区晚白垩世存在大规模花岗岩成岩-锡成矿事件。  相似文献   

20.
1 Introduction Since the Guilaizhuang gold deposit was discovered in the 1980s, the Tongshi magmatic complex has attracted attention since it exhibits a spatial-temporal relationship to gold mineralization. In the past ten years, a number of detailed fundamental researches have been carried out on the complex, Guilaizhuang gold deposit and their relationships (Qiu et al., 1994; Lin et al., 1996; Yan et al., 1996; Xu et al., 1999; Kong et al., 2001; Shun et al., 2001). Up to date, some res…  相似文献   

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