首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 65 毫秒
1.
This contribution presents data for laser ablation multicollector ICP‐MS (LA‐MC‐ICP‐MS) analyses of NIST SRM 610 and 612 glasses with the express purpose of examining the Pb isotope homogeneity of these glasses at the ～ 100 μm spatial scale, relevant to in situ analysis. Investigation of homogeneity at these scales is important as these glasses are widely used as calibrators for in situ measurements of Pb isotope composition. Results showed that at the levels of analytical uncertainty obtained, there was no discernable heterogeneity in Pb isotope composition of NIST SRM 610 and also most probably for NIST SRM 612. Traverses across the ～ 1.5 mm glass wafers supplied by NIST, consisting of between 75 and 133 individual measurements, showed no compositional outliers at the two standard deviation level beyond those expected from population statistics. Overall, the measured Pb isotope ratios from individual traverses across NIST SRM 610 and 612 wafers closely approximate single normally‐distributed populations, with standard deviations similar to the average internal uncertainty for individual measurement blocks. Further, Pb isotope ratios do not correlate with Tl/Pb ratios measured during the analysis, suggesting that regions of volatile element depletion (marked by low Tl/Pb) in these glasses are not associated with changes in Pb isotope composition. For NIST SRM 610 there also appeared to be no variation in Pb isotope composition related to incomplete mixing of glass base and trace element spike during manufacture. For NIST SRM 612 there was some dispersion of measured ratios, including some in a direction parallel to the expected mixing line for base‐spike mixing. However, there was no significant correlation parallel to the mixing line. At this time this cannot be unequivocally demonstrated to result from glass heterogeneity, but it is suggested that NIST SRM 610 be preferred for standardising in situ Pb isotope measurements. Data from this study also showed significantly better accuracy and somewhat better precision for ratios corrected for mass bias by external normalisation to Pb isotope ratios measured in bracketing calibrators compared to mass bias corrected via internal normalisation to measured 205Tl/203Tl, although the Tl isotopic composition of both glasses appears to be homogeneous.  相似文献   

2.
J.L. Paquette  M. Tiepolo   《Chemical Geology》2007,240(3-4):222-237
Monazite [(LREE)PO4], a common accessory mineral in magmatic and metamorphic rocks, is complementary to zircon in U–Th–Pb geochronology. Because the mineral can record successive growth phases it is useful for unravelling complex geological histories. A high spatial resolution is required to identify contrasted age domains that may occur at the crystal-scale. Bulk mineral techniques such as ID-TIMS, applied to single monazite grains recording multiple overgrowths or isotope resetting can result in partly scattered discordant analytical points that produce inaccurate intercept ages. Laser ablation (LA)-ICPMS has been demonstrated to be a useful technique for U–Th–Pb dating of zircons, and this study tests its analytical capabilities for dating monazite. A sector field high resolution ICPMS coupled with a 193 nm ArF excimer laser ablation microprobe is capable of achieving a high spatial resolution and producing stable and reliable isotope measurements.

The U–Th–Pb systematic was applied to monazite grains from several samples: a lower Palaeozoic lens from high-grade terrains in Southern Madagascar, Neogene hydrothermal crystals from the Western Alps, a Palaeoproterozoic very high temperature granulite from central Madagascar and a Variscan leucogranite from Spain, directly on a polished thin section. The major aim was to compare and/or reproduce TIMS and EMP ages of monazite from a variety of settings and ages. The three independent 206Pb/238U, 207Pb/235U and 208Pb/232Th ratios and ages were calculated. Isotope fractionation effects (mass bias, laser induced fractionation) were corrected using a chemically homogeneous and U–Pb concordant monazite as external standard.

This study demonstrates that excimer laser ablation (ELA)-ICPMS allows U–Th–Pb dating of monazite with a high level of repeatability, accuracy and precision as well as rapidity of analysis. A spatial resolution almost comparable to that of EMP in terms of crater width (5 μm) produced precise 208Pb/232Th, 206Pb/238U and 207Pb/235U ratios for dating Palaeozoic to Precambrian monazites. The advantages of (ELA)-ICPMS isotope dating are precision, accuracy and the ability to detect discordance. In the case of late Miocene hydrothermal monazites from the Alps, a larger spot size of 25 μm diameter is required, and precise and accurate ages were obtained only for 208Pb/232Th systematics. Results from the Variscan granite show that in situ U–Th–Pb dating of monazites with (ELA)-ICPMS is possible using a 5 μm spot directly on thin sections, so that age data can be placed in a textural context.  相似文献   


3.
Lead isotopes are a powerful and versatile tool to elucidate fundamental geological problems related to the formation and evolution of continental crust. K-feldspar is a popular target for Pb isotope measurement as it is prevalent in many rock types and tends to capture the initial Pb isotope composition of its parental magma. We present data for a new Pb isotope reference material: Albany K-feldspar; as well as updated data for Shap K-feldspar. Results of Pb double-spike TIMS for Albany K-feldspar are 206Pb/204Pb = 16.7872 ± 0.0062, 207Pb/204Pb = 15.5640 ± 0.0056, and 208Pb/204Pb = 36.6600 ± 0.0168 (2s). TIMS measurement results for Shap K-feldspar indicate two isotopically distinct Pb populations. LA-MC-ICP-MS, with a spatial resolution as high as 15 μm, indicates a homogeneous Pb isotopic composition in Albany K-feldspar. In accord with previous studies, our results show that scatter in the measured Pb isotope ratios, related to the low natural isotopic abundance of 204Pb, along with the effect of isobaric 204Hg-204Pb interference, increases at lower count rates. However, the mean Pb isotope ratios measured via LA-MC-ICP-MS using a range of spot sizes are in excellent agreement with TIMS results thus highlighting the feasibility of Pb isotope determination via LA-MC-ICP-MS to access geological information preserved in small crystals, including mineral inclusions.  相似文献   

4.
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   

5.
U-Pb isotopic analyses using TIMS and Laser Ablation-Multi Collector-ICP-MS were carried out on columbite-tantalite minerals from three suites of rare-element (Li, Cs, Ta) pegmatites in the Superior Province of Canada. Conventional TIMS analyses of these columbite-tantalite crystals produce scattered data and reverse discordance even after HF leaching of the grains prior to dissolution, possibly reflecting the incomplete removal of the open-system metamict segments during sample preparation. LA-MC-ICP-MS analyses of unleached, primary columbite free from inclusions and alteration give consistent and precise (<0.5%) Pb-Pb ages, demonstrating the utility of this approach. However, normal and reverse discordance is also observed in U-Pb data from LA-MC-ICP-MS analyses. This discordance represents either U-Pb mobilisation during recent weathering, sample preparation and/or an analytical artefact originating from variable elemental fractionation between U and Pb during ablation and ionisation that itself may have its origin in the contrasting metamictization of the dated columbite and the monazite standard used. Best age estimates of columbite from pegmatites in the Superior Province are; 2670±5 Ma for the Pakeagama Lake pegmatite, 2644±7 Ma for the Separation Rapids group, and 2665±8 Ma for the Mavis Lake group. The ages broadly show that the rare-element pegmatites are temporally synchronous with adjacent peraluminous granites.Editorial responsibility: T.L. Grove  相似文献   

6.
LA-MC-ICP-MS锆石微区原位U-Pb定年技术   总被引：297，自引：33，他引：264  
利用激光多接收等离子体质谱(LA-MC-ICP-MS)技术对30～1 065 Ma的系列锆石进行了详细的定年研究.包含离子计数器的多接收系统使得不同质量数的同位素信号可以同时静态接收,并且不同质量数的峰基本上都是平坦的,进而可以获得高精度的数据,均匀锆石颗粒207Pb/206Pb、206Pb/238U、207Pb/235U比值的测试精度(2σ)均为2%左右,对锆石标准的定年精度和准确度在1%(2σ)左右;不同质量数同位素信号的同时静态接收使得剥蚀时间缩短,剥蚀深度变浅,相比LA-ICP-MS方法,提高了激光剥蚀的空间分辨率.对5个锆石标准和2个实际样品的测试表明,206Pb/235U年龄测定误差在1%(2σ)以内,定年结果在误差范围内与前人报道值完全一致,测试精度达到国际同类实验室先进水平.  相似文献   

7.
In this study we evaluated the capability of a 213 nm laser ablation system coupled to a quadrupole-based ICP-MS in delivering accurate and precise U-Pb ages on zircons and monazites. Four zircon samples ( ca. 50 Ma to ca. 600 Ma) and four monazite samples ( ca. 30 Ma to ca. 1390 Ma) of known ages were analysed utilising laser ablation pits with diameters of 20 μm and 60 μm. Instrument mass bias and laser induced time-dependent elemental fractionation were corrected for by calibration against a matrix-matched reference material. Tera-Wasserburg plots of the calculated U-Pb data were employed to assess, and correct for, common Pb contributions. The results indicated that the LA-ICP-MS technique employed in this study allowed precise and accurate U-Pb isotope dating of zircon and monazite on sample areas 20 μm in diameter. At this spot size, the precisions achieved for single spot 206Pb/238U ages, were better than 5% (2s) for monazites and zircons with ages down to 30 Ma and 50 Ma, respectively. The precisions reported are comparable to those generally reported in SIMS and LA-MC-ICP-MS U-Pb isotope determinations.  相似文献   

8.
Isotope dilution determinations of Lu, Hf, Zr, Ta and W are reported for nine test portions (five for W) of NIST SRM 610 and 612 glass wafers. Additionally, all test portions were analysed for their Hf isotope compositions. In general, high field strength elemental (HFSE) distributions in NIST SRM 610 and 612 were reproducible to ～± 1%, except for Zr (± 5%) in NIST SRM 612, and absolute reported concentrations agreed with previously published values, but with higher precision. The slightly worse reproducibility of Zr in NIST SRM 612 compared to other HFSE is interpreted to result from analytical scatter, rather than sample inhomogeneity. The analyses demonstrated elemental homogeneity for both glass wafers for samples of 1–2 mg with respect to the precision of the method, i.e., ± 1% or better. Average Hf isotope compositions for both glass wafers agreed within uncertainty and the weighted average of all determinations yielded a mean 176Hf/177Hf ratio of 0.282111 ± 0.000009 (95% confidence level). However, although mean values for NIST SRM 610 and 612 agreed within analytical limits, NIST SRM 610 test portions showed a tendency of systematically elevated isotope composition of ～ 0.5 ?Hf units when compared to NIST SRM 612, which may indicate a slightly more radiogenic Hf isotope composition of NIST SRM 610. The results of this study suggest that NIST SRM 610 and 612 are valuable calibrators for HFSE in situ analyses within the given uncertainties.  相似文献   

9.
We present data on the concentration, the isotope composition and the homogeneity of boron in NIST silicate glass reference materials SRM 610 and SRM 612, and in powders and glasses of geological reference materials JB-2 (basalt) and JR-2 (rhyolite). Our data are intended to serve as references for both microanalytical and wet-chemical techniques. The δ11 B compositions determined by N-TIMS and P-TIMS agree within 0.5% and compare with SIMS data within 2.5%. SIMS profiles demonstrate boron isotope homogeneity to better than δ11 B = 2% for both NIST glasses, however a slight boron depletion was detected towards the outermost 200 μm of the rim of each sample wafer. The boron isotope compositions of SRM 610 and SRM 612 were indistinguishable. Glasses produced in this study by fusing JB-2 and JR-2 powder also showed good boron isotope homogeneity, both within and between different glass fragments. Their major element abundance as well as boron isotope compositions and concentrations were identical to those of the starting composition. Hence, reference materials (glasses) for the in situ measurement of boron isotopes can be produced from already well-studied volcanic samples without significant isotope fractionation. Oxygen isotope ratios, both within and between wafers, of NIST reference glasses SRM 610 and SRM 612 are uniform. In contrast to boron, significant differences in oxygen isotope compositions were found between the two glasses, which may be due to the different amounts of trace element oxides added at ten-fold different concentration levels to the silicate matrix.  相似文献   

10.
本文以稀土矿床中的常见副矿物氟碳铈矿为研究对象,通过优化实验条件和仪器参数,分别采用激光剥蚀多接收电感耦合等离子体质谱法(LA-MC-ICP-MS)和同位素稀释热电离质谱法(ID-TIMS)对氟碳铈矿样品SAM进行U-Pb定年技术研究,并将此两种方法得到的结果进行对比。LA-MC-ICP-MS得到的U-Pb年龄为(409±18)Ma(N=27,MSWD=4.5),ID-TIMS得到的206Pb/238U U-Pb年龄为(407.8±3.3)Ma(N=3,MSWD=0.029),两种方法得到的U-Pb年龄结果在误差范围内一致。通过比较两种方法的实验流程和结果,总结了各自的优缺点,为氟碳铈矿U-Pb定年方法选择提供了参考依据。  相似文献   

11.
Collision‐related granitoid batholiths, like those of the Hercynian and Himalayan orogens, are mostly fed by magma derived from metasedimentary sources. However, in the late Neoproterozoic calcalkaline (CA) batholiths of the Arabian–Nubian Shield (ANS), which constitutes the northern half of the East African orogen, any sedimentary contribution is obscured by the juvenile character of the crust and the scarcity of migmatites. Here, we use paired in situ LASS‐ICP‐MS measurements of U–Th–Pb isotope ratios and REE contents of monazite and xenotime and SHRIMP‐RG analyses of separated zircon to demonstrate direct linkage between migmatites and granites in the northernmost ANS. Our results indicate a single prolonged period of monazite growth at 640–600 Ma, in metapelites, migmatites and peraluminous granites of three metamorphic suites: Abu‐Barqa (SW Jordan), Roded (S Israel) and Taba–Nuweiba (Sinai, Egypt). The distribution of monazite dates and age zoning in single monazite grains in migmatites suggest that peak thermal conditions, involving partial melting, prevailed for c. 10 Ma, from 620 to 610 Ma. REE abundances in monazite are well correlated with age, recording garnet growth and garnet breakdown in association with the prograde and retrograde stages of the melting reactions, respectively. Xenotime dates cluster at 600–580 Ma, recording retrogression to greenschist facies conditions as garnet continued to destabilize. Phase equilibrium modelling and mineral thermobarometry yield P–T conditions of ~650–680°C and 5–7 kbar, consistent with either water‐fluxed or muscovite‐breakdown melting. The expected melt production is 8–10 vol.%, allowing a melt connectivity network to form leading to melt segregation and extraction. U–Pb ages of zircon rims from leucosomes indicate crystallization of melt at 610 ± 10 Ma, coinciding with the emplacement of a vast volume of CA granites throughout the northern ANS, which were previously considered post‐collisional. Similar monazite ages (c. 620 Ma) retrieved from the amphibolite facies Elat schist indicate that migmatites are the result of widespread regional rather than local contact metamorphism, representing the climax of the East African orogenesis.  相似文献   

12.
Polyphase metamorphic paragneisses from the drill core of the continental deep drilling project (KTB; NW Bohemian Massif) are characterized by peak pressures of about 8 kbar (medium‐P metamorphism) followed by strain accumulation at T >650 °C, initially by dislocation creep and subsequently by diffusion creep. U–Pb monazite ages and Rb–Sr whole‐rock data vary in the dm‐scale, indicating Ordovician and Mid‐Devonian metamorphic events. Such age variations are closely interconnected with dm‐scale domainal variations of microfabrics that indicate different predominant deformation mechanisms. U–Pb monazite age variations dependent on microfabric domains exceed grain‐size‐dependent age variations. In ‘mylonitic domains’ recording high magnitudes of plastic strain, dislocation creep and minor static annealing, monazite yields concordant and near concordant Lower Ordovician U–Pb ages, and the Rb–Sr whole‐rock system shows isotopic disequilibrium at an mm‐scale. In ‘mineral growth/mobilisate domains’, in which diffusive mass transfer was a major strain‐producing mechanism promoting diffusion creep of quartz and feldspar, and in which static recrystallization (annealing) reduced the internal free energy of the strained mineral aggregates, concordant U–Pb ages are Mid‐Devonian. Locally, in such domains, Rb–Sr dates among mm3‐sized whole‐rock slabs reflect post‐Ordovician resetting. In ‘transitional domains’, the U–Pb‐ages are discordant. We conclude that medium‐P metamorphism occurred at 484±2 Ma, and a second metamorphic event at 380–370 Ma (Mid‐Devonian) caused progressive strain in the rocks. Dislocation creep at high rates, even at high temperatures, does not reset the Rb–Sr whole‐rock system, while diffusion creep at low rates and stresses (i.e. low ε/Deff ratios), static annealing and the presence of intergranular fluids locally assist resetting. At temperatures above 650 °C, diffusive Pb loss did not reset Ordovician U–Pb monazite ages, and in domains of overall high imposed strain rates and stresses, resetting was not assisted by dynamic recrystallization/crystal plasticity. However, during diffusion creep at low rates, Pb loss by dissolution and precipitation (‘recrystallization’) of monazite produces discordance and Devonian‐concordant U–Pb monazite ages. Hence, resetting of these isotope systems reflects neither changes of temperature nor, directly, the presence or absence of strain.  相似文献   

13.
Anomalous Pb isotope ratios measured by Inductively Coupled Plasma Mass Spectrometry in terrigenous marine sediments (<63 μm fraction) from the Gulf of Carpentaria originated from depositional mixing of clay/silt with average modern crustal Pb isotope ratios and detrital monazite with high 208Pb/206Pb and low 207Pb/206Pb. This interpretation is supported by strong correlations between Pb isotope ratio and Th, U and light rare‐earth element concentrations in the sediments as well as by monazite compositional data. A likely source of the detrital monazite is the western portion of the Georgetown Inlier of mainly Proterozoic S‐type granitic rocks. A clear distinction between Pb isotope ratios in sediments deposited from the Norman and Bynoe Rivers in the southeast Gulf of Carpentaria and the persistence of catchment‐specific Pb isotope ratios 45 km offshore suggest that Pb isotope data are useful in tracing the provenance of terrigenous offshore sediments when the source rocks of catchments show sufficient chemical and/or mineralogical variation.  相似文献   

14.
147Sm-143Nd放射性同位素体系在地球科学研究中得到了广泛的应用,经典的同位素稀释-热表面电离质谱法(ID-TIMS)一直是Sm-Nd同位素高精度测定的基准技术,但具有耗时长、成本高、样品需求量大等缺点,并且难以揭示微观尺度单矿物所蕴含的地球化学信息。近年来兴起的微区原位分析,具有简单、快速、高空间分辨率的特点,可以从微米尺度示踪岩浆和热液的起源及演化过程。本文通过同时测定Sm和Nd同位素质量分馏系数,实现144Sm对144Nd干扰的准确校正,获得了人造玻璃、磷灰石、榍石、独居石等几种不同基体标准样品(NIST610、Durango、MAD-2、BLR-1、117531)精确的143Nd/144Nd比值,与推荐值在误差范围内一致。然而,由于Sm和Nd元素性质的差异,在激光剥蚀和质谱电离过程中会产生明显的元素分馏,导致147Sm/144Nd很难进行精确校正,本文通过在进样系统中引入液态气溶胶,有效克服了基体效...  相似文献   

15.
The NIST glass certified reference materials, SRM 610-617, have been widely adopted by the geological community as calibration samples for a variety of in situ trace element analytical techniques. There is now an urgent requirement for similar reference materials for in situ isotopic analytical techniques. We have analysed SRM 610, 612 and 614 for their Pb, Sr and Nd isotopic compositions using thermal ionisation mass spectrometry. Large differences in isotopic composition were observed between each CRM, suggesting a significant trace element content in the initial starting material (base glass). As a result, isotopic compositions for one CRM cannot be extrapolated to another, and each must be calibrated for use independently. We present the first compilation of working values for these glasses.  相似文献   

16.
The Teplá Crystalline unit (TCU), western Bohemian Massif, proves highly suitable for studying the effects of differential metamorphic reworking on the U–Th–Pb systematics in monazite, as the overprint of Variscan regional metamorphism onto high-grade Cadomian paragneisses intensifies progressively towards the northwest. Although variably hampered by scarcity, small size, and low uranium contents of monazite, isotope dilution–thermal ionisation mass spectrometry of monazite from paragneisses from the garnet, staurolite, and kyanite zones of the TCU gives a narrow 206Pb/238U age range from 387 to 382 Ma for Variscan peak metamorphism. These data are supported by 382–373 Ma monazite ages derived from electron microprobe analyses. Inheritance of older components in grains from the central TCU imply major “resetting” of pre-Variscan monazite around 380 Ma, possibly due to widespread garnet growth during Variscan metamorphism, which led to the consumption of pre-Variscan high-Y monazite and subsequent growth of new low-Y monazite. Concordant 498–494 Ma monazite ages in a migmatitic paragneiss close to the adjacent Mariánské Lázně Complex (MLC) grew in response to metagabbro emplacement in the MLC from 503 to 496 Ma and not during either Cadomian or Variscan regional metamorphism. Backscatter imaging and electron microprobe analyses reveal that discordant monazite of the migmatite comprises a mix of various age domains that range from ca. 540 to 380 Ma. Combined evidence presented here suggests that instead of Pb loss by volume diffusion, the apparent resetting of the U–Th–Pb systematics in monazite rather involves new crystal growth or regrowth by recrystallisation and dissolution/reprecipitation.  相似文献   

17.
National Institute of Science and Technology (NIST) silicate glass SRM 610 is widely used as a certified reference material for various micro-analytical techniques such as SIMS or laser ablation ICP-MS. SRM 610 has been nominally doped with sixty one trace elements at the 500 μg g−1 level, but certified concentration data exist for only a few of these elements. This study reports concentration data for fifty nine trace elements obtained by ICP-MS, SSMS, LIMS, TIMS, INAA, AAS, and PIXE analyses of two different SRM 610 wafers. Most elements fall within a 10% band around a median value of about 440 μg g−1. The REE concentrations are shown to be constant to 3% (1 σ), thus emphasizing the value of SRM 610 as a reference material for REE analyses.
Comparison of our values with published data suggests that different SRM 610 wafers are, within errors, chemically identical for most elements. Exceptions to this general rule appear to be restricted to elements which were partly lost during the production of the glass, e.g. Ag and Br. On the basis of six independent determinations of Rb concentrations, which are systematically lower by a few percent than the reported NIST value, we argue that the certified Rb concentration may not be representative for all distributed SRM 610 wafers.  相似文献   

18.
We performed in situ Th-Pb dating of monazite in upper amphibolite facies pelitic schist from the Grouse Creek Mountains in northwest Utah. Sixty-six ages from inclusions in four garnet grains range from 37 to 72 Ma and decrease with radial distance from garnet cores. The age range of 30 matrix monazite grains overlaps and extends to younger ages than inclusions (25-58 Ma). The monazite grains are not intersected by cracks in the garnets, through which dissolution, reprecipitation or Pb loss might occur, and are generally too small (<20 μm) to allow for more than one age determination on any one grain. Processes that might explain inclusion ages that decrease with radial distance from garnet cores include: (1) Pb diffusion in monazite, (2) dissolution and reprecipitation of monazite, and (3) co-crystallization of monazite and garnet. After consideration of these possibilities, it is concluded that the co-crystallization of monazite and garnet is the most plausible, with monazite neoblasts deriving REEs from the breakdown of muscovite. Garnet ages derived by regression of the inclusion ages and assuming a constant rate of volume increase during garnet growth yield model ages with a maximum difference between core and rim of 22 m.y.  相似文献   

19.
Barbados岛珊瑚礁高精度铀系年龄及讨论   总被引：3，自引：0，他引：3       下载免费PDF全文
马志邦  王兆荣 《地质科学》1999,34(1):116-122
应用同位素稀释法热电离质谱(TIMS)技术测定珊瑚礁的高精度铀系年龄。通过对BarbadosⅢ、Ⅳ阶地等样品分析,RendezvousHil和Curacao+6m的TIMS年龄分别为129.2±1.2kaB.P.和125.4±1.1kaB.P.,对应深海沉积物氧同位素第5期5e段的高海面;Kendal山阶地为208.1±1.9kaB.P.,可能代表7c间冰期高海平面的时代。该结果与Edwards等测定同一阶地的年龄一致,与α谱法数据在误差范围内吻合。另外,探讨了初始铀同位素比值的变化,并对TIMS年龄的可靠性做了评价。  相似文献   

20.
 The relative importance of thermal diffusion versus new growth or recrystallization on U-Pb isotopic data from sphene is assessed through a study of amphibolites and granite gneisses within the contact aureole of the Red Mountain pluton, Laramie anorthosite complex, Wyoming. Samples were collected along a traverse approximately perpendicular to the margin of the intrusion over a distance of 0.13 to 2.65 km from the contact. The 207Pb/206Pb ages of sphene from amphibolite samples range between 1.43 Ga, the intrusive age of the Red Mountain pluton, to 1.78 Ga, the age of regional metamorphism. The 207Pb/206Pb ages of sphene in rocks metamorphosed above 700° C are within error of the intrusive age of the pluton, and appear to have resulted from diffusional resetting of preexisting sphene and the metamorphic growth of additional sphene at 1.43 Ga. At greater distance from the contact the 207Pb/206Pb ages range from 1.45 to 1.72 Ga. This 300 million year spread in ages is interpreted to result from two periods of sphene growth, one produced during regional metamorphism at 1.78 Ga and another generation of newly grown or recrystallized sphene that formed during contact metamorphism at 1.43 Ga. These two age populations may be identified on the basis of petrographic textures, the morphologies and color differences of grain separates as well as by the U-Pb systematics. In rocks metamorphosed to temperatures less than 700° C, sphene growth was the dominant process controlling the response of the U-Pb isotope system to contact metamorphism. Sphene grew well outside the zone of obvious contact metamorphism. The U-Pb sphene ages were reset by diffusion only at high temperatures, supporting the experimentally determined closure temperature estimates for the U-Pb system in sphene of around 650° C (Cherniak 1993). This study demonstrates that U-Pb ages of sphene can be used to date metamorphism not only in areas with a simple geologic history, such as igneous intrusion or single metamorphic or deformational events, but also to date multiple events so long as different generations of sphene can be identified and separated. Received: 22 August 1995 / Accepted: 17 April 1996  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号