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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.
《Gondwana Research》2009,15(4):587-596
We developed a 238U–206Pb⁎ and 207Pb⁎–206Pb⁎ zircon dating method using a Cameca NanoSIMS NS50 ion microprobe. A 7-to 9-nA O− primary beam was used to sputter a 15-μm crater, and secondary positive ions were extracted for mass analysis using the Mattauch–Herzog geometry. The multicollector system was modified to detect 90Zr+, 204Pb+, 206Pb+, 238U16O+, and 238U16O2+ ions simultaneously. A mass resolution of about 4000 at 10% peak height and with a flat peak top was attained, and the sensitivity of Pb was about 4 cps·nA− 1·ppm− 1. A multicrystal zircon standard (QGNG) from South Australia with a U–Pb age of 1842 Ma was used as a reference for Pb+/UO+–UO2+/UO+ calibration, and on the basis of the positive correlation between these ratios, we determined the sample 206Pb/238U ratios. 207Pb/206Pb ratios were measured by magnetic scanning in single-collector mode. The standard zircons 91500, from Canada, and SL13, from Sri Lanka, were analyzed against QGNG. Observed 238U–206Pb⁎ and 207Pb⁎–206Pb⁎ ages agreed well with published ages within experimental error. Then, 16 zircon grains in a metamorphic rock from Nagasaki, Japan, were analyzed. Observed ages were compatible with SHRIMP ages, suggesting that the NanoSIMS with a 15-μm probe diameter is suitable for ion microprobe U–Pb zircon dating.  相似文献   

3.
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   

4.
Using a state‐of‐the‐art 193 nm‐LA‐MC‐ICP‐MS system and with careful control of analytical procedures, the long term external reproducibility and accuracy of the ages Phanerozoic zircons measured over a period of months using calibrator bracketing for the 206Pb/238U and 207Pb/206Pb ages were ca. 1% (2 RSD) if a single reference zircon was used for the matrix‐matched calibration. When different reference zircons were used for the calibration, suspicious systematic shifts in the obtained ages were observed and thus a reduction in the overall accuracy of the dating method became obvious. Such shifts were within a few percent range of the U‐Pb and Pb/Pb ages and seemed to vary independently of zircon age and composition. A “test of accuracy” experiment was conducted reducing instrumental effects as far as possible by analysing five different reference zircons mounted on a single mount eight times during the same session. An identical protocol was used for all analyses, with unchanged instrument parameters and with ion beam intensities kept as identical as possible. For data reduction, every zircon served consecutively as the reference zircon for calibration, with the others in the batch treated as unknowns. The known reference age and the four calculated ages obtained using the four other RMs for calibration were then compared. Even using such a strict analytical protocol, shifts in 206Pb/238U, 207Pb/235U and 207Pb/206Pb ratios were still present. They varied non‐systematically and ranged from ?4.35% to 3.08% for the investigated age range (1065 Ma to 226 Ma). Assuming the absence of instrumental effects (i.e., memory, dead‐time correction, non‐linearity of ion counters and interdetector calibration, crystallographic orientation, ablation cell geometry and setup, gas flows), the observed shifts were attributed to matrix and/or ablation related effects. It is proposed that non‐spectral matrix effects in the Ar plasma torch resulted in non‐uniform signal enhancement (or depression?) leading to shifts both in elemental and Pb isotopic ratios. Additionally, the ablated particle size distribution could be an important factor controlling plasma conditions and thus mass bias and fractionation. Until such effects are well understood and controlled, it would seem that any LA‐ICP‐MS zircon U‐Pb and 207Pb/206Pb age determination cannot be meaningfully interpreted at below a ca. 3% to 4% (2 RSD) confidence level.  相似文献   

5.
On the basis of internal structures, laser ablation U–Pb ages and trace element compositions, the origin of zircon in jadeitite in the Nishisonogi metamorphic rocks was examined. The zircon comprises euhedral zoned cores overgrown by euhedral rims. The cores contain inclusions of muscovite, quartz, albite and possibly K‐feldspar, yield 238U–206Pb ages of 126 ± 6 Ma (±2 SD, n = 45, MSWD = 1.0), and have Th/U ratios of 0.48–1.64. The rims contain inclusions of jadeite, yield 238U–206Pb ages of 84 ± 6 Ma (±2 SD, n = 14, MSWD = 1.1), and have Th/U ratios of <0.06. The cores are richer in Y, Th, Ti and rare earth elements (REEs), but the rims are richer in Hf and U. Chondrite‐normalized REE patterns of the cores indicate higher SmN/LaN ratios, lower YbN/GdN ratios and larger positive Ce anomalies compared with those of the rims. Thus, the cores and rims have different 238U–206Pb ages and trace element compositions, suggesting two stages of zircon growth. Although the 238U–206Pb ages of the rims are consistent with the reported 40Ar/39Ar spot‐fusion ages of matrix muscovite in the jadeitite, the 238U–206Pb ages of the cores are older. The mineral inclusions and high Th/U ratios in the cores are best explained by crystallization from felsic magma. Therefore, the cores are considered relicts from igneous precursor rocks. The rims surrounding the inherited cores possibly precipitated from aqueous fluids during jadeitite formation. The elevated U concentrations in the rims suggest that infiltration of external fluids was responsible for the precipitation. This study provides an example of jadeitite formation by metasomatic replacement of a protolith.  相似文献   

6.
The Cycladic blueschist belt in the central Aegean Sea has experienced high‐pressure (HP) metamorphism during collisional processes between the Apulian microplate and Eurasia. The general geological and tectonometamorphic framework is well documented, but one aspect which is yet not sufficiently explored is the importance of HP mélanges which occur within volcano‐sedimentary successions. Unresolved issues concern the range in magmatic and metamorphic ages recorded by mélange blocks and the significance of eventual pre‐Eocene HP metamorphism. These aspects are here addressed in a U‐Pb zircon study focusing on the block–matrix association exposed on the island of Syros. Two gneisses from a tectonic slab of this mélange, consisting of an interlayered felsic gneiss‐glaucophanite sequence, yielded zircon 206Pb/238U ages of 240.1 ± 4.1 and 245.3 ± 4.9 Ma, respectively, similar to Triassic ages determined on zircon in meta‐volcanic rocks from structurally coherent sequences elsewhere in the Cyclades. This strongly suggests that parts of these successions have been incorporated in the mélanges and provides the first geochronological evidence that the provenance of mélange blocks/slabs is neither restricted to a single source nor confined to fragments of oceanic lithosphere. Zircon from a jadeitite and associated alteration zones (omphacitite, glaucophanite and chlorite‐actinolite rock) all yielded identical 206Pb/238U ages of c. 80 Ma. Similar Cretaceous U‐Pb zircon ages previously reported for mélange blocks have been interpreted by different authors to reflect magmatic or metamorphic ages. The present study adds a further argument in favour of the view that zircon formed newly in some rock types at c. 80 Ma, due to hydrothermal or metasomatic processes in a subduction zone environment, and supports the interpretation that the Cycladic blueschist belt records both Cretaceous and Eocene HP episodes and not only a single Tertiary HP event.  相似文献   

7.
Columbite-tantalite LA-ICP-MS U-Pb dating is a fast and useful method to determine the age of rare-metal deposits and fingerprint the provenance of columbite-tantalite ore concentrates. Accurate LA-ICP-MS U-Pb dating requires matrix-matched reference materials. We analysed three columbite-tantalite samples (SN3, HND and RL2) from China using ID-TIMS and LA-ICP-MS to assess their potential as reference materials for in situ U-Pb dating. Coltan 139 and these three columbite-tantalite samples with variable compositions yielded internally consistent LA-ICP-MS U-Pb ages when using each other for calibration and the weighted mean 206Pb/238U ages are comparable to respective ID-TIMS ages. Composition-dependent U-Pb fractionation seems to be insignificant under the LA-ICP-MS conditions used. Sample SN3 has a low percentage of heterogeneity for 206Pb/238U ages (4%) with low common Pb contributions (f206 < 1%) and shows a good potential in calibrating unknown samples as primary reference material for LA-ICP-MS analysis. Samples RL2 and HND have altered sections characterised by high LREE contents, flat LREE patterns and old 206Pb/238U apparent ages, and are not suited as reference materials. The low 207Pb/206Pb intercepts for samples RL2 and HND lack geological meaning but provide strong evidence that the disturbed U-Pb systematics with anomalous apparent 206Pb/238U ages is a secondary feature.  相似文献   

8.
In this article, we document a detailed analytical characterisation of zircon M127, a homogeneous 12.7 carat gemstone from Ratnapura, Sri Lanka. Zircon M127 has TIMS‐determined mean U–Pb radiogenic isotopic ratios of 0.084743 ± 0.000027 for 206Pb/238U and 0.67676 ± 0.00023 for 207Pb/235U (weighted means, 2s uncertainties). Its 206Pb/238U age of 524.36 ± 0.16 Ma (95% confidence uncertainty) is concordant within the uncertainties of decay constants. The δ18O value (determined by laser fluorination) is 8.26 ± 0.06‰ VSMOW (2s), and the mean 176Hf/177Hf ratio (determined by solution ICP‐MS) is 0.282396 ± 0.000004 (2s). The SIMS‐determined δ7Li value is ?0.6 ± 0.9‰ (2s), with a mean mass fraction of 1.0 ± 0.1 μg g?1 Li (2s). Zircon M127 contains ~ 923 μg g?1 U. The moderate degree of radiation damage corresponds well with the time‐integrated self‐irradiation dose of 1.82 × 1018 alpha events per gram. This observation, and the (U–Th)/He age of 426 ± 7 Ma (2s), which is typical of unheated Sri Lankan zircon, enable us to exclude any thermal treatment. Zircon M127 is proposed as a reference material for the determination of zircon U–Pb ages by means of SIMS in combination with hafnium and stable isotope (oxygen and potentially also lithium) determination.  相似文献   

9.
The isotopic (U-Pb, 238U-235U, 234U-238U) and chemical study of whole-rock samples and finegrained fractions of rocks in a vertical section of the terrigenous sequence at the Dybryn uranium deposit in the Khiagda ore field shows that a wide U-Pb isotopic age range (26.9-6.5 Ma) is caused by oxidation and disturbance of the U-Pb isotopic system in combination with protracted uranium ore deposition. The oxidation of rocks resulted in the loss of uranium relative to lead and eventually to an overestimated 206Pb/238U age at sites with a low U content. The 238U/235U ratios in the studied samples are within the range of 137.74–137.88. Samples with a high uranium content are characterized by a decreasing 238U/235U ratio with a decrease in 207Pb/235U and 206Pb/238U ages. A nonequilibrium 234U/238U ratio in most studied samples furnishes evidence for young (<1.5 Ma) transformation of the Miocene uranium ore, which is responsible for uranium migration and its redeposition.  相似文献   

10.
Zircons from metamorphosed granites exposed near Qinglongshan have δ18OVSMOW values of −7 to 0‰ in both grain rims and cores. The concordant 238U/206Pb ages of zircon cores are 684 to 754 Ma with rims at 221 Ma. Discordant 238U/206Pb ages range from 242 to 632 Ma. Results demonstrate a Neoproterozoic age for the origin of the Qinglongshan oxygen and hydrogen isotope anomaly. The low δ18O values were imprinted on the rocks by a hydrothermal system charged with meteoric water from a cold climate. Groundwater circulation was driven by heat from cooling granitic magma. The geologic age of the hydrothermal system correlates with that of the Nantuo tillite in the Sinian strata of the South China block, suggesting that Qinglongshan’s cold climate may be a manifestation of Neoproterozoic “snowball Earth.”  相似文献   

11.
We present multitechnique U‐Pb geochronology and Hf isotopic data from zircon separated from rapakivi biotite granite within the Eocene Golden Horn batholith in Washington, USA. A weighted mean of twenty‐five Th‐corrected 206Pb/238U zircon dates produced at two independent laboratories using chemical abrasion‐isotope dilution‐thermal ionisation mass spectrometry (CA‐ID‐TIMS) is 48.106 ± 0.023 Ma (2s analytical including tracer uncertainties, MSWD = 1.53) and is our recommended date for GHR1 zircon. Microbeam 206Pb/238U dates from laser ablation‐inductively coupled plasma‐mass spectrometry (LA‐ICP‐MS) and secondary ion mass spectrometry (SIMS) laboratories are reproducible and in agreement with the CA‐ID‐TIMS date to within < 1.5%. Solution multi‐collector ICP‐MS (MC‐ICP‐MS) measurements of Hf isotopes from chemically purified aliquots of GHR1 yield a mean 176Hf/177Hf of 0.283050 ± 17 (2s, n = 10), corresponding to a εHf0 of +9.3. Hafnium isotopic measurements from two LA‐ICP‐MS laboratories are in agreement with the solution MC‐ICP‐MS value. The reproducibility of 206Pb/238U and 176Hf/177Hf ratios from GHR1 zircon across a variety of measurement techniques demonstrates their homogeneity in most grains. Additionally, the effectively limitless reserves of GHR1 material from an accessible exposure suggest that GHR1 can provide a useful reference material for U‐Pb geochronology of Cenozoic zircon and Hf isotopic measurements of zircon with radiogenic 176Hf/177Hf.  相似文献   

12.
We developed a 238U–206Pb and 207Pb–206Pb zircon dating method using a Cameca NanoSIMS NS50 ion microprobe. A 7-to 9-nA O− primary beam was used to sputter a 15-μm crater, and secondary positive ions were extracted for mass analysis using the Mattauch–Herzog geometry. The multicollector system was modified to detect 90Zr+, 204Pb+, 206Pb+, 238U16O+, and 238U16O2+ ions simultaneously. A mass resolution of about 4000 at 10% peak height and with a flat peak top was attained, and the sensitivity of Pb was about 4 cps·nA− 1·ppm− 1. A multicrystal zircon standard (QGNG) from South Australia with a U–Pb age of 1842 Ma was used as a reference for Pb+/UO+–UO2+/UO+ calibration, and on the basis of the positive correlation between these ratios, we determined the sample 206Pb/238U ratios. 207Pb/206Pb ratios were measured by magnetic scanning in single-collector mode. The standard zircons 91500, from Canada, and SL13, from Sri Lanka, were analyzed against QGNG. Observed 238U–206Pb and 207Pb–206Pb ages agreed well with published ages within experimental error. Then, 16 zircon grains in a metamorphic rock from Nagasaki, Japan, were analyzed. Observed ages were compatible with SHRIMP ages, suggesting that the NanoSIMS with a 15-μm probe diameter is suitable for ion microprobe U–Pb zircon dating.  相似文献   

13.
Most monazite reference materials (RMs) for in situ U‐Pb geochronology are rich in Th; however, many hydrothermal ore deposits contain monazite that is low in trace element contents, including Th, U and Pb. Because of potential problems with matrix effects and the lack of appropriate matrix‐matched RMs, such variations can bias dating of hydrothermal deposits. In this paper, we describe a polycrystalline low‐U and low‐Th Diamantina monazite from the Espinhaço Range, SE Brazil. It has a U‐Pb ID‐TIMS weighted mean 207Pb*/235U ratio of 0.62913 ± 0.00079, 206Pb*/238U of 0.079861 ± 0.000088 and 207Pb*/206Pb* of 0.057130 ± 0.000031, yielding a weighted mean 206Pb*/238U date of 495.26 ± 0.54 Ma (95% c.l.). In situ dates acquired with different methods (LA‐(Q, SF, MC)‐ICP‐MS and SIMS) are within uncertainty of the ID‐TIMS data. U‐Pb LA‐(Q, MC)‐ICP‐MS runs, using Diamantina as a primary RM, reproduced the ages of other established RMs within < 1% deviation. The LA‐MC‐ICP‐MS analyses yielded homogeneous Sm‐Nd isotopic compositions (143Nd/144Nd = 0.511427 ± 23, 2s; 147Sm/144Nd = 0.1177 ± 13, 2s) and εNd(495 Ma) of ?18.7 ± 0.5 (2s). SIMS oxygen isotope determinations showed measurement reproducibility better than ± 0.3‰ (2s), confirming Diamantina's relative homogeneity at test portion masses below 1 ng.  相似文献   

14.
目前应用LA-MC-ICPMS分析熔体包裹体Pb同位素,由于没有同时测试U和Th的信号,导致熔体包裹体Pb同位素的研究仅局限于中生代以来的样品。本文应用LA-MC-ICPMS分析了玻璃样品以及存在显著U-Th衰变影响的古老熔体包裹体的Pb同位素组成,评价了U/Pb和Th/Pb分析误差对初始Pb同位素比值校正的影响。实验中以国际玻璃标样NKT-1G为外部标样,采用"标样-样品-标样法"进行仪器漂移和质量歧视校正,结果表明,国际玻璃标样BHVO-2G、TB-1G的208Pb/206Pb和207Pb/206Pb分析精度优于0.30%(2RSD),与推荐值的偏差小于0.30%,然而232Th/206Pb和238U/206Pb分析结果显示了较大分散性(外精度约5.0%)。根据误差传递计算,样品的年龄对初始铅的误差有很大影响。对于古生代以来的样品(年龄小于540 Ma),即使测试的232Th/206Pb和238U/206Pb与真值偏差达到10%,经过U-Th衰变校正后的Pb同位素比值与真值的偏差依然小于0.80%。因此本方法可以将熔体包裹体等地质样品的Pb同位素研究由新生代样品(年龄小于65 Ma)扩展到古生代样品。  相似文献   

15.
Zircon U-Pb ages and geochemical analytical results are presented for the volcanic rocks of the Naozhigou, Ergulazi, and Sidaogou Formations in the Linjiang area, southeastern Jilin Province to constrain the nature of magma source and their tectonic settings. The Naozhigou Formation is composed mainly of andesite and rhyolite and its weighted mean 206Pb/238U age for 13 zircon grains is 222±1 Ma. The Ergulazi Formation consists of basaltic andesite, basaltic trachyandesite, and andesite, and six grains give a weighted mean 206Pb/238U age of 131±4 Ma. The Sidaogou Formation consists mainly of trachyandesite and rhyolite, and six zircon grains yield a weighted mean 206Pb/238U age of 113±4 Ma. The volcanic rocks have SiO2=60.24%–77.46%, MgO=0.36%–1.29% (Mg#=0.32–0.40) for the Naozhigou Formation, SiO2=51.60%–59.32%, MgO=3.70%–5.54% (Mg#=0.50–0.60) for the Ergulazi Formation, and SiO2=58.28%–76.32%, MgO=0.07%–1.20% (Mg#=0.14–0.46) for the Sidaogou Formation. The trace element analytical results indicate that these volcanic rocks are characterized by enrichment in light rare earth elements (LREEs) and large ion lithophile elements (LILEs), relative depletion in heavy rare earth elements (HREEs) and high field strength elements (HFSEs, Nb, Ta, and Ti), and negative Eu anomalies. Compared with the primitive mantle, the Mesozoic volcanic rocks in the Linjiang area have relatively high initial 87Sr/86Sr ratios (0.7053-0.7083) and low εNd(t) values (?8.38 to ?2.43), and display an EMII trend. The late Triassic magma for the Naozhigou Formation could be derived from partial melting of a newly accretional crust with the minor involvement of the North China Craton basement and formed under an extensional environment after the collision of the Yangtze Craton and the North China Craton. The Early Cretaceous volcanic rocks for the Ergulazi and Sidaogou Formations could be formed under the tectonic setting of an active continental margin related to the westward subduction of the Izanagi plate.  相似文献   

16.
We introduce a potential new working reference material – natural zircon megacrysts from an Early Pliocene alkaline basalt (from Penglai, northern Hainan Island, southern China) – for the microbeam determination of O and Hf isotopes, and U–Pb age dating. The Penglai zircon megacrysts were found to be fairly homogeneous in Hf and O isotopes based on large numbers of measurements by LA-multiple collector (MC)-ICP-MS and SIMS, respectively. Precise determinations of O isotopes by isotope ratio mass spectrometry (IRMS) and Hf isotopes by solution MC-ICP-MS were in good agreement with the statistical mean of microbeam measurements. The mean δ18O value of 5.31 ± 0.10‰ (2s) by IRMS and the mean 176Hf/177Hf value of 0.282906 ± 0.0000010 (2s) by solution MC-ICP-MS are the best reference values for the Penglai zircons. SIMS and isotope dilution-TIMS measurements yielded consistent 206Pb/238U ages within analytical uncertainties, and the preferred 206Pb/238U age was found to be 4.4 ± 0.1 Ma (95% confidence interval). The young age and variably high common Pb content make the Penglai zircons unsuitable as a primary U–Pb age reference material for calibration of unknown samples by microbeam analysis; however, they can be used as a secondary working reference material for quality control of U–Pb age determination for young (particularly < 10 Ma) zircon samples.  相似文献   

17.
The Penglaitan section, as the Global Stratotype Section for the Guadalupian–Lopingian boundary (GLB), displays continuous deposition with a complete succession of pelagic conodont zones across the GLB. However, there is no reliable radiometric age from the Penglaitan section itself to constrain the GLB. Here, we report SIMS zircon U‐Pb ages from two bentonite layers (Bed 7c) in the Penglaitan Global Stratotype Section near the GLB. The sample PL‐62‐1 yields a weighted mean 238U/206Pb age of 257.1 ± 2.2 Ma, and the sample PL‐62‐2 yields a weighted mean 206Pb/238U age of 257.0 ± 4.2 Ma. Therefore, we consider 257.0–257.1 Ma as the age of deposition of Bed 7c (the end of the C. postbitteri postbitteri conodont Zone, ca. 86 cm above the GLB), and, considering the depositional rate of chert, we suggest 258.6 Ma as the age of the GLB. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

18.
In the Orlica‐?nie?nik complex at the NE margin of the Bohemian Massif, high‐pressure granulites occur as isolated lenses within partially migmatized orthogneisses. Sm–Nd (different grain‐size fractions of garnet, clinopyroxene and/or whole rock) and U–Pb [isotope dilution‐thermal ionization mass spectrometry (ID‐TIMS) single grain and sensitive high‐resolution ion microprobe (SHRIMP)] ages for granulites, collected in the surroundings of ?ervený D?l (Czech Republic) and at Stary Giera?tów (Poland), constrain the temporal evolution of these rocks during the Variscan orogeny. Most of the new ages cluster at c. 350–340 Ma and are consistent with results previously reported for similar occurrences throughout the Bohemian Massif. This interval is generally interpreted to constrain the time of high‐pressure metamorphism. A more complex evolution is recorded for a mafic granulite from Stary Giera?tów and concerns the unknown duration of metamorphism (single, short‐lived metamorphic cycle or different episodes that are significantly separated in time?). The central grain parts of zircon from this sample yielded a large spread in apparent 206Pb/238U SHRIMP ages (c. 462–322 Ma) with a distinct cluster at c. 365 Ma. This spread is interpreted to be indicative for variable Pb‐loss that affected magmatic protolith zircon during high‐grade metamorphism. The initiating mechanism and the time of Pb‐loss has yet to be resolved. A connection to high‐pressure metamorphism at c. 350–340 Ma is a reasonable explanation, but this relationship is far from straightforward. An alternative interpretation suggests that resetting is related to a high‐temperature event (not necessarily in the granulite facies and/or at high pressures) around 370–360 Ma, that has previously gone unnoticed. This study indicates that caution is warranted in interpreting U–Pb zircon data of HT rocks, because isotopic rejuvenation may lead to erroneous conclusions.  相似文献   

19.
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   

20.

The Progress Granite is one of numerous S‐type granitoid plutons exposed in the Larsemann Hills region, southwest Prydz Bay, east Antarctica. The granite was emplaced into a migmatitised pelitic to felsic paragneiss sequence during a regional high‐grade transpressional event (D2) that pre‐dates high‐grade extension (D3). SHRIMP (II) U‐Pb dating for two occurrences of the Progress Granite from D2 and D3 structural domains gives 206Pb/238U ages of 516.2 ± 6.8 Ma and 514.3 ± 6.7 Ma, respectively. These ages are interpreted as crystallisation ages for the Progress Granite and confirm Early Palaeozoic orogenesis in the Larsemann Hills region. This orogen appears to have evolved during continental convergence and is probably responsible for widespread radiogenic isotopic resetting and the near‐complete exhumation of the adjacent northern Prince Charles Mountains which evolved during a ca 1000 Ma event. The identification of a major Early Palaeozoic orogen in Prydz Bay allows tentative correlation of other domains of Early Palaeozoic tectonism both within the east Antarctic Shield and other, once contiguous, Gondwana fragments and illustrates the potential complexity inherent within intercratonic mobile belts. One such possibility, tentatively offered here, suggests a continuous belt of Early Palaeozoic tectonism from Prydz Bay eastward to the West Denman Glacier region and into the Leeuwin complex of Western Australia.  相似文献   

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