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1.
Here we report on a set of six apatite reference materials (chlorapatites MGMH#133648, TUBAF#38 and fluorapatites MGMH#128441A, TUBAF#37, 40, 50) which we have characterised for their chlorine isotope ratios; these RMs span a range of Cl mass fractions within the apatite Ca10(PO4)6(F,Cl,OH)2 solid solution series. Numerous apatite specimens, obtained from mineralogical collections, were initially screened for 37Cl/35Cl homogeneity using SIMS followed by δ37Cl characterisation by gas source mass spectrometry using both dual‐inlet and continuous‐flow modes. We also report major and key trace element compositions as determined by EPMA. The repeatability of our SIMS results was better than ± 0.10‰ (1s) for the five samples with > 0.5 % m/m Cl and ± 0.19‰ (1s) for the low Cl abundance material (0.27% m/m). We also observed a small, but significant crystal orientation effect of 0.38‰ between the mean 37Cl/35Cl ratios measured on three oriented apatite fragments. Furthermore, the results of GS‐IRMS analyses show small but systematic offset of δ37ClSMOC values between the three laboratories. Nonetheless, all studied samples have comparable chlorine isotope compositions, with mean 103δ37ClSMOC values between +0.09 and +0.42 and in all cases with 1s ≤ ± 0.25.  相似文献   

2.
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   

3.
A new natural zircon reference material SA01 is introduced for U‐Pb geochronology as well as O and Hf isotope geochemistry by microbeam techniques. The zircon megacryst is homogeneous with respect to U‐Pb, O and Hf isotopes based on a large number of measurements by laser ablation‐inductively coupled plasma‐mass spectrometry (LA‐ICP‐MS) and secondary ion mass spectrometry (SIMS). Chemical abrasion isotope dilution thermal ionisation mass spectrometry (CA‐ID‐TIMS) U‐Pb isotopic analyses produced a mean 206Pb/238U age of 535.08 ± 0.32 Ma (2s, n = 10). Results of SIMS and LA‐ICP‐MS analyses on individual shards are consistent with the TIMS ages within uncertainty. The δ18O value determined by laser fluorination is 6.16 ± 0.26‰ (2s, n = 14), and the mean 176Hf/177Hf ratio determined by solution MC‐ICP‐MS is 0.282293 ± 0.000007 (2s, n = 30), which are in good agreement with the statistical mean of microbeam analyses. The megacryst is characterised by significant localised variations in Th/U ratio (0.328–4.269) and Li isotopic ratio (?5.5 to +7.9‰); the latter makes it unsuitable as a lithium isotope reference material.  相似文献   

4.
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   

5.
In situ U-Pb geochronology and hafnium, oxygen and zirconium isotope measurements in zircons using laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) and ion microprobe techniques can provide essential isotopic data to constrain geological evolutionary histories. Developing reliable zircon reference materials is the cornerstone for in situ zircon chronology and isotopic studies. In this study, the homogeneity of U-Pb ages and Hf-O-Zr isotope ratios in three Sri Lankan zircon megacrysts (SLZA, SLZB and SLZC) were investigated using multiple analytical methods. The obtained U, Th, Pb and Hf mass fractions of the SLZA zircon were 839 ± 56 μg g-1 (1s), 151 ± 15 μg g-1 (1s), 198 ± 28 μg g-1 (1s) and 8635 ± 286 μg g-1 (1s), respectively. The mass fractions of U, Th, Pb and Hf in the SLZB zircon were 1106 ± 106 μg g-1 (1s), 331 ± 61 μg g-1 (1s), 376 ± 57 μg g-1 (1s) and 9673 ± 976 μg g-1 (1s), respectively. The U, Th, Pb and Hf mass fractions determined in the SLZC zircon were 551 ± 35 μg g-1 (1s), 111 ± 8 μg g-1 (1s), 129 ± 18 μg g-1 (1s) and 7881 ± 393 μg g-1 (1s), respectively. The chemical abrasion isotope dilution thermal ionisation mass-spectrometry (CA-ID-TIMS) method yielded a Th-corrected weighted mean 206Pb/238U age of 556.94 ± 1.29 Ma (95% conf., n = 5) for the SLZA zircon, 552.90 ± 1.29 Ma (95% conf., n = 7) for the SLZB zircon and 560.83 ± 1.29 Ma (95% conf., n = 7) for the SLZC zircon. The obtained Hf isotopic compositions of the SLZA, SLZB and SLZC zircons determined with the solution MC-ICP-MS method were 0.281651 ± 0.000014 (2s, n = 10), 0.281704 ± 0.000008 (2s, n = 10) and 0.281676 ± 0.000006 (2s, n = 10), respectively. The obtained O isotopes of the SLZA and SLZB zircons measured with the laser fluorination method were 12.14 ± 0.56‰ (2s, n = 4) and 11.91 ± 0.30‰ (2s, n = 4), respectively. The Zr isotopes of the SLZA, SLZB and SLZC zircons determined with double spike TIMS analysis yielded mean δ94/90ZrSRM3169 values of -0.03 ± 0.06‰ (2s, n = 10), -0.03 ± 0.04‰ (2s, n = 10) and 0.00 ± 0.07‰ (2s, n = 8), respectively. The SLZA zircon can be used as a primary reference or quality control material for microbeam U-Pb, Hf and Zr isotope measurements because of its slight heterogeneity. The U-Pb, Hf and Zr isotopic compositions of the SLZB and SLZC megacrysts were homogeneous. The O isotopic compositions in the SLZA and SLZB zircon were slightly dispersed, indicating that these two megacrysts can only serve as secondary reference materials for microbeam O isotope measurements.  相似文献   

6.
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   

7.
Granitoid plutons are often difficult to radiometrically date precisely due to the possible effects of protracted and complex magmatic evolution, crustal inheritance, and/or partial re-setting of radiogenic clocks. However, apart from natural/geological issues, methodological and analytical problems may also contribute to blurring geochronological data. This may be exemplified by the Variscan Karkonosze Pluton (SW Poland). High-precision chemical abrasion (CA) ID-TIMS zircon data indicate that the two main rock types, porphyritic and equigranular, of this igneous body were both emplaced at ca. 312 Ma, while field evidence points to a younger age for the latter. This is in contrast to the earlier reported SIMS (SHRIMP) zircon dates that scattered mainly between ca. 322 and 302 Ma. In an attempt to overcome this dispersion, at least in part caused by radiogenic lead loss, the CA technique was used before SHRIMP analysis. The 206Pb/238U age obtained in this way from a sample of porphyritic granite is 322 ± 3 Ma, ~16 Ma older than the untreated zircons; another porphyritic sample yielded a mean age of 319 ± 3 Ma, and the mean age was 318 ± 4 Ma for an equigranular granite sample – all three somewhat older than the age obtained by ID-TIMS. Older SIMS dates of ca. 318–322 Ma might indicate either faint inheritance or that zircon domains crystallized during earlier stages of Karkonosze igneous evolution. The ID-TIMS results have been used to re-assess the whole-rock Rb–Sr data. Excluding a porphyritic granite with excess radiogenic 87Sr, it appears that isotopic homogeneity was achieved for most samples during the 312 Ma event, as shown by a pooled 21-point isochron with an age of 311 ± 3 Ma and an initial 86Sr/86Sr of 0.7067 ± 4. Local crustal contamination by stopping of metapelitic material might account for the more radiogenic Sr isotope signature observed in biotite-rich schlieren. A critical re-evaluation of all available SHRIMP data using the ID-TIMS age of 312 Ma as a benchmark suggests that the observed scatter may be partly attributed to analytical and methodological problems, in particular failing to distinguish subtly discordant spots from truly concordant ones, which is a serious limitation of the microbeam analytical approach. Other likely pitfalls contributing to geochronological scatter are identified in the published Re–Os ages on molybdenite and the 40Ar/39Ar data on micas. A scenario postulating a 15–20 milliion year evolution of the Karkonosze Pluton cannot be established on the basis of available geochronological data, which rather supports a brief igneous event, although a more protracted pre-emplacement evolution is possible. A short timescale for crystallization of large igneous bodies, as suggested by the ID-TIMS data from the Karkonosze Granite, is in line with models of transport of granitic magmas through dikes to form large plutons.  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.
磷灰石微区原位LA-MC-ICP-MS U-Pb同位素定年   总被引：5，自引：0，他引：5  
利用激光剥蚀多接收器电感耦合等离子体质谱法(LA-MC-ICP-MS), 建立了磷灰石微区原位U-Pb同位素定年新方法, 本文给出了这一新方法的分析流程, 报道了利用这一新方法对5个磷灰石样品的分析结果, 并应用同位素稀释-热电离质谱法(ID-TIMS)对一些样品定年结果进行了验证。磷灰石工作标样SDG的U-Pb同位素年龄: (1596±15) Ma (MSWD=1.5, n=7, LA-MC-ICP-MS), (1602±13) Ma (MSWD=0.578, n=5, ID-TIMS); 某铁矿石中磷灰石的LA-MC-ICP-MS U-Pb同位素年龄: (125±14) Ma (MSWD=0.68, n=25), (124.2±3.5) Ma (MSWD=1.5, n=37); 新疆阿尔金地区片麻岩中磷灰石的LA-MC-ICP-MS U-Pb同位素年龄: (250.8±3.9) Ma (MSWD=8.6, n=26), (245.4±2.9) Ma (MSWD=2.1, n=39)。  相似文献   

10.
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   

11.
The large tonnage Maoling gold deposit (25 t @ 3.2 g/t) is located in the southwest Liaodong Peninsula, North China Craton. The deposit is hosted in the Paleoproterozoic metamorphic rocks. Four stages of mineralization were identified in the deposit: (stage I) quartz-arsenopyrite ± pyrite, (stage II) quartz-gold- arsenopyrite-pyrrhotite, (stage III) quartz-gold- polymetallic sulfide, and (stage IV) quartz-calcite-pyrrhotite. In this paper, we present fluid inclusion, C-H-O-S-Pb-He-Ar isotope data, zircon U-Pb, and gold-bearing sulfide (i.e. arsenopyrite and pyrrhotite) Rb-Sr age of the Maoling gold deposit to constrain its genesis and ore-forming mechanism. Three types of fluid inclusions were distinguished in quartz-bearing veins, including liquid-rich two-phase (WL type), gas-rich two-phase (GL type), and daughter mineral-bearing fluid inclusions (S type). Fluid inclusions data show that the homogenization at temperatures 197 to 372 °C for stage I, 126 to 319 °C for stage II, 119 to 189 °C for stage III, and 115 to 183 °C for stage IV, with corresponding salinities of 3.7 to 22.6 wt.%, 4.7 to 23.2 wt.%, 5.3 to 23.2 wt.%, and 1.7 to 14.9 wt.% NaCl equiv., respectively. Fluid boiling was the critical factor controlling the gold and associated sulfide precipitation at Maoling. Hydrogen and oxygen stable isotopic analyses for quartz yielded δ18O = ?5.0‰ to 9.8‰ and δ D = ?133.5‰ to ?77.0‰. Carbon stable isotopic analyses for calcite and ankerite yielded δ13C = ?2.3‰ to ?1.2‰ and O = 7.9‰ to 14.1‰. The C-H-O isotope data show that the ore-forming fluids were originated from magmatic water with meteoric water input during mineralization. Hydrothermal inclusions in arsenopyrite have 3He/4He ratios of 0.002 Ra to 0.054 Ra, and 40Ar/36Ar rations of 1225 to 3930, indicating that the ore-forming fluids were dominantly derived from crustal sources almost no mantle input. Sulfur isotopic values of Maoling fine-grained granite range from 6.‰1 to 9.8‰, with a mean of 7.7‰, δ34S values of arsenopyrite from the mineralized phyllite (host rock) range from 8.9‰ to 10.6‰, with a mean of 10.0‰, by contrast, δ34S values of sulfides from ore vary between 4.3‰ and 10.6‰, with a mean of 6.8‰, suggesting that sulfur was mainly originated from both the host rock and magma. Lead radioactive isotopic analyses for sulfides yielded 206Pb/204Pb = 15.830–17.103, 207Pb/204Pb = 13.397–15.548, 208Pb/204Pb = 35.478–36.683, and for Maoling fine-grained granite yielded 206Pb/204Pb = 18.757–19.053, 207Pb/204Pb = 15.596–15.612, and 208Pb/204Pb = 38.184–39.309, also suggesting that the ore-forming materials were mainly originated from the host rocks and magma. Zircon U-Pb dating demonstrates that the Maoling fine-grained granite was emplaced at 192.7 ± 1.8 Ma, and the host rock (mineralized phyllite) was emplaced at some time after 2065.0 ± 27.0 Ma. Arsenopyrite and pyrrhotite give Rb–Sr isochron age of 188.7 ± 4.5 Ma, indicating that both magmatism and mineralization occurred during the Early Jurassic. Geochronological and geochemical data, together with the regional geological history, indicate that Early Jurassic magmatism and mineralization of the Maoling gold deposit occurred during the subducting Paleo-Pacific Plate beneath Eurasia, and the Maoling gold deposit is of the intrusion-related gold deposit type.  相似文献   

12.
The age of the Katera Group, which occupies a large area in the western North Muya Range and occurs 100–150 km east of the Uakit Group, is a debatable issue. Based on geological correlations with reference sections of the Baikal Group and Patom Complex, the Katera and Uakit groups were previously considered nearly coeval units and assigned to Late Precambrian (Khomentovskii and Postnikov, 2002; Salop, 1964). This was supported partly by the Sm–Nd model datings (Rytsk et al., 2007, 2009, 2011). Finds of the Paleozoic flora substantiated the revision of age of the Uakit Group and its assignment to the Late Devonian–Early Carboniferous (Gordienko et al., 2010; Minina, 2003, 2012, 2014). We have established that Sr and C isotopic compositions in carbonates of these groups differ drastically, as suggested by their different ages. Sediments of the Nyandoni Formation (Katera Group), which contains carbonates characterized by minimum values of 87Sr/86Sr = 0.7056 and maximum values of δ13C = 4.9‰, were accumulated in the first half of Late Riphean (800–850 Ma ago), whereas the overlying Barguzin Formation (87Sr/86Srmin = 0.70715, δ13Cmax= 10.5‰) was deposited at the end of Late Riphean (700–750 Ma). Judging from the isotope data, the Nerunda Formation (Uakit Group), which contains carbonates with characteristics matching the most rigorous criteria of fitness for the chemostratigraphic correlation (Sr content up to 4390 μg/g, Mn/Sr < 0.1, δ18O = 23.0 ± 1.8‰), was deposited at the end of Vendian ~550–540 Ma ago). The sequence includes thick typical carbonate horizons with very contrast carbon isotopic compositions: the lower unit has anomalous high δ13C values (5.8 ± 1.0‰); the upper unit, by anomalous low δ13C values (–5.2 ± 0.5‰]). Their Sr isotopic composition is relatively homogeneous (87Sr/86Sr = 0.7084 ± 0.0001) that is typical of the Late Vendian ocean. The S isotopic composition of pyrites from the Nyandoni Formation (Katera Group) (δ34S = 14.1 ± 6.8‰) and pyrites from the Mukhtunny Formation (Uakit Group) (δ34S = 0.7 ± 1.4‰) does not contradict the C and Sr isotopic stratigraphic data.  相似文献   

13.
Alkaline intrusions in the eastern Shandong Province consist of quartz monzonite and granite. U-Pb zircon ages, geochemical data, and Sr-Nd-Pb isotopic data for these rocks are reported in the present paper. Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) U-Pb zircon analyses yielded consistent ages ranging from 114.3?±?0.3 to 122.3?±?0.4 Ma for six samples of the felsic rocks. The felsic rocks are characterised by a wide range of chemical compositions (SiO2?=?55.14–77.63 wt. %, MgO?=?0.09–4.64 wt. %, Fe2O3?=?0.56–7.6 wt. %, CaO?=?0.40–5.2 wt. %), light rare earth elements (LREEs) and large ion lithophile elements (LILEs) (i.e., Rb, Pb, U) enrichment, as well as significant rare earth elements (HREEs) and heavy field strength (HFSEs) (Nb, Ta, P and Ti) depletion, various and high (87Sr/86Sr) i ranging from 0.7066 to 0.7087, low ε Nd (t) values from ?14.1 to ?17.1, high neodymium model ages (TDM1?=?1.56–2.38Ga, TDM2?=?2.02–2.25Ga), 206Pb/204Pb?=?17.12–17.16, 207Pb/204Pb?=?15.44–15.51, and 208Pb/204Pb?=?37.55–37.72. The results suggested that these rocks were derived from an enriched crustal source. In addition, the alkaline rocks also evolved as the result of the fractionation of potassium feldspar, plagioclase, +/? ilmenite or rutile and apatite. However, the alkaline rocks were not affected by crustal contamination. Moreover, the generation of the alkaline rocks can be attributed to the structural collapse of the Sulu organic belt due to various processes.  相似文献   

14.
U-Pb zircon geochronology is increasingly called upon to achieve the resolution of absolute time at the 0.1% to 1% level for rocks of Phanerozoic to Hadean age. Doing so requires accurate calibration of the several methods (conventional isotope dilution thermal ionization mass spectrometry [ID-TIMS], Pb evaporation, high-resolution ion microprobe [e.g. SHRIMP], and laser ablation inductively coupled plasma mass spectrometry [LA-ICPMS]) currently in use, in numerous laboratories, for the analysis of U and Pb isotopes in accessory minerals. Toward this end, the geochronological community would benefit from the establishment, distribution and widespread analysis of one or more standard reference materials. Among the candidates is natural zircon from the Duluth Complex anorthositic series of the Midcontinent Rift system of North America. These zircons, first dated by conventional ID-TIMS at 1099.1 ± 0.5 Ma, have been subsequently adopted as a geochronological standard by a number of high resolution ion microprobe facilities. A new and independent analysis of the systematics of a large set of single zircons (n = 27) from the same mineral separate yields indistinguishable 207Pb/206Pb, upper intercept, and U-Pb concordia dates for the AS3 zircons. The concordia date, based on a subset of 12 concordant and equivalent zircons, of 1099.1 ± 0.2 Ma (±1.2 Ma considering systematic uncertainties in Pb/U tracer calibration and U decay constants) is indistinguishable from previously published results. We further document the absence of inherited Pb in the AS3 zircons, and discuss strategies for avoiding certain domains within the AS3 zircons exhibiting small amounts of radiation-induced, surface and fracture-correlated, recent Pb loss. Although the AS3 zircons do not represent the ideal (and elusive) homogeneous closed U-Pb system, we conclude that these and similar zircons from the Duluth Complex anorthositic series can provide a suitable geochronological reference standard for numerous U-Pb zircon analytical methods, given appropriate preparation guided by the results of this study. Our high-precision data set also serves as a useful confirmatory test of the currently accepted U decay constants.  相似文献   

15.
The Taoxihu deposit (eastern Guangdong, SE China) is a newly discovered Sn polymetallic deposit. Zircon U-Pb dating yielded 141.8 ± 1.0 Ma for the Sn-bearing granite porphyry and 145.5 ± 1.6 Ma for the biotite granite batholith it intruded. The age of the granite porphyry is consistent (within error) with the molybdenite Re–Os isochron age (139.0 ± 1.1 Ma) of the Sn mineralization, indicating a temporal link between the two. Geochemical data show that the granite porphyry is weakly peraluminous, contain high Si, Na and K, low Fe, Mg, Ca and P, and relatively high Rb/Sr and low K/Rb values. The rocks are enriched in Rb, Th, U, K, and Pb and depleted in Ba, Sr, Ti and Eu, resembling highly fractionated I-type granites. They contain bulk rock initial 87Sr/87Sr of 0.707371–0.707730 and εNd(t) of −5.17 to −4.67, and zircon εHf(t) values from −6.67 to −2.32, with late Mesoproterozoic TDM2 ages for both Nd and Hf isotopes. This suggests that the granite porphyry was likely formed by the partial melting of the crustal basement of Mesoproterozoic overall residence age with minor mantle input.δ34SCDT values of the Taoxihu chalcopyrite and pyrite range from 0.1 to 2.1‰ (average: 0.9‰), implying a dominantly magmatic sulfur source. The 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb ratios of the Taoxihu sulfide ores are 18.497–18.669, 15.642–15.673 and 38.764–38.934, respectively, indicating a mainly upper continental crustal lead source with minor mantle contribution. The highly fractionated and reduced (low calculated zircon Ce4+/Ce3+ and EuN/EuN1 values) nature of the ore-forming granitic magma may have facilitated the Sn enrichment and played a key role in the Sn mineralization. We propose that the ore-forming fluids at Taoxihu were of magmatic-hydrothermal origin derived from the granite porphyry, and that both the granite porphyry and the Sn mineralization were likely formed in an extensional setting, possibly related to the subduction slab rollback of the Paleo-Pacific Plate.  相似文献   

16.
Accurate ion microprobe analysis of oxygen isotope ratios in garnet requires appropriate reference materials to correct for instrumental mass fractionation that partly depends on the garnet chemistry (matrix effect). The matrix effect correlated with grossular, spessartine and andradite components was characterised for the Cameca IMS 1280HR at the SwissSIMS laboratory based on sixteen reference garnet samples. The correlations fit a second‐degree polynomial with maximum bias of ca. 4‰, 2‰ and 8‰, respectively. While the grossular composition range 0–25% is adequately covered by available reference materials, there is a paucity of them for intermediate compositions. We characterise three new garnet reference materials GRS2, GRS‐JH2 and CAP02 with a grossular content of 88.3 ± 1.2% (2s), 83.3 ± 0.8% and 32.5 ± 3.0%, respectively. Their micro scale homogeneity in oxygen isotope composition was evaluated by multiple SIMS sessions. The reference δ18O value was determined by CO2 laser fluorination (δ18OLF). GRS2 has δ18OLF = 8.01 ± 0.10‰ (2s) and repeatability within each SIMS session of 0.30–0.60‰ (2s), GRS‐JH2 has δ18OLF = 18.70 ± 0.08‰ and repeatability of 0.24–0.42‰ and CAP02 has δ18OLF = 4.64 ± 0.16‰ and repeatability of 0.40–0.46‰.  相似文献   

17.
《地学前缘(英文版)》2020,11(5):1593-1608
The Gejiu-Bozushan-Laojunshan W-Sn polymetallic metallogenic belt(GBLB) in southeast Yunnan Province is an important part of the southwestern Yangtze Block in South China.Tin polymetallic mineralization in this belt includes the Niusipo,Malage,Songshujiao,Laochang and Kafang ore fields in the Gejiu area which are spatially and temporally associated with the Kafang-Laochang and Songshujiao granite plutons.These granites are characterized by variable A/CNK values(mostly 1.1,except for two samples with 1.09),high contents of SiO_2(74.38-76.84 wt.%) and Al_2 O_3(12.46-14.05 wt.%) and variable CaO/Na_2 O ratios(0.2-0.65) as well as high zircon δ~(18)O values(7.74‰-9.86‰),indicative of S-type affinities.These rocks are depleted in Rb,Th,U,Ti,LREE[(La/Yb)N=1.4-20.51],Ba,Nb,Sr,and Ti and display strong negative Eu and Ba anomalies.The rocks possess high Rb/Sr and Rb/Ba ratios,relatively low initial ~(87)Sr/~(86)Sr ratios(0.6917-0.7101),and less radiogenic εNd(t)values(-8.0 to-9.1).The zircon grains from these rocks show negative ε_(Hf)(t) values in the range of-3.7 to-9.9 with mean T_(DM2)(Nd) and T_(DM2)(Hf) values of 1.57 Ga and 1.55 Ga.They show initial ~(207)Pb/~(204)Pb ranging from15.69 to 15.71 and ~(206)Pb/~(204)Pb from 18.36 to 18.70.Monazite from Songshujiao granites exhibits higher U and lower Th/U ratios,lower δ~(18)O values and higher ε_(Hf)(t) values than those of the zircon grains in the KafangLaochang granites.The geochemical and isotopic features indicate that the Laochang-Kafang granites originated by partial melting of Mesoproterozoic crustal components including biotite-rich metapelite and metagraywacke,whereas the Songshujiao granites were derived from Mesoproterozoic muscovite-rich metapelite crustal source.Most zircon grains from the Songshujiao,Laochang and Kafang granites have high-U concentrations and their SIMS U-Pb ages show age scatter from 81.6 Ma to 88.6 Ma,80.7 Ma to 86.1 Ma and 82.3 Ma to 87.0 Ma,suggesting formation earlier than the monazite and cassiterite.Monazite SIMS U-Pb ages and Th-Pb ages of three same granite samples are consistent and show yielded 206 Pb/~(238)U ages of 83.7 ± 0.6 Ma,83.7±0.6 Ma,and 83.4±0.6 Ma,and ~(208)Pb/~(232)Th ages of 83.2 ± 0.5 Ma,83.8 ± 0.4 Ma,and 83.5±0.9 Ma,which are within the range of the SIMS zircon U-Pb ages from these rocks.The data constrain the crystallization of the granites at ca.83 Ma.In situ U-Pb dating of two cassiterite samples from the cassiterite-sulfide ore in the Songshujiao ore field and Kafang ore field,and two from the cassiterite-oxide+cassiterite bearing dolomite in the Laochang ore field yielded weighted mean 206 Pb/~(238)U ages of 83.5±0.4 Ma(MSWD=0.6),83.5 ± 0.4 Ma(MSWD=0.5),83.6 ±0.4 Ma(MSWD=0.6) and 83.2 ±0.7 Ma(MSWD=0.6),respectively.Combined with geological characteristics,the new geochronological data indicate that the formation of the granites and Sn polymetallic deposits are coeval.We correlate the magmatic and metallogenic event with lithospheric thinning and asthenosphere upwelling in continental extension setting in relation to the eastward subduction of the Neo-Tethys beneath the Sanjiang tectonic domain during Late Cretaceous.  相似文献   

18.
Two quartz samples of igneous origin, UNIL‐Q1 (Torres del Paine Intrusion, Chile) and BGI‐Q1 (Shandong province, China), were calibrated for their oxygen isotope composition for SIMS measurements. UNIL‐Q1 and BGI‐Q1 were evaluated for homogeneity using SIMS. Their reference δ18O values were determined by CO2 laser fluorination. The average δ18O value found for UNIL‐Q1 is 9.8 ± 0.06‰ and that for BGI‐Q1 is 7.7 ± 0.11‰ (1s). The intermediate measurement precision of SIMS oxygen isotope measurements was 0.32–0.41‰ (2s; UNIL‐Q1) and 0.40–0.48‰ (2s; BGI‐Q1), respectively. While less homogeneous in its oxygen isotope composition, BGI‐Q1 is also suitable for SIMS trace element measurements.  相似文献   

19.
This paper presents the results of combined studies of geochronology, geochemistry, whole rock Sr-Nd and zircon Hf-O isotopes carried out upon the rhyodacite and ignimbrite of Shangshu village, Shangyu town and Shanghupeng village of Jiangshan City in Zhejiang Province, along the northwestern side of the Jiangshan–Shaoxing suture. SHRIMP zircon U-Pb dating of samples in the three areas yielded weighted mean 206 Pb/238 U ages of 842.8 ± 6.9 Ma and 850.0 ± 7.3 Ma, 839 ± 9 Ma and 832.2 ± 8.1 Ma, 828.3 ± 8.5 Ma and 836.9 ± 9.9 Ma, respectively. These ages are older than the volcanic rocks of the Shangshu Formation dated at around 780 Ma distributed in Fuyang City, Hangzhou City, Kaihua County, etc. The volcanic rocks generally have high SiO2(54.08–76.80 wt%) and Al2 O3(12.40–21.31 wt%), low Fe2 O3(0.68–8.92 wt%), MgO(0.29–2.49 wt%), CaO(0.12–2.86 wt%), TiO2(0.10–1.59 wt%) and P2 O5(0.01–0.39 wt%), with variable total alkalis(K2 O + Na2 O =5.42–8.29 wt%). There exists a clear negative correlation between SiO2 and P2 O5. The volcanic rocks have A/CNK ratios of 1.03–2.77 and thus are peraluminous. They are characterized by enrichment in LREE, Rb, Ba, Zr, Hf, K, Th, La, U and depletion in Nb, Sr, P, Ti, with distinct LREE and HREE fractionation of(La/Yb)N values of 5.68–11.67, and with a moderate negative Eu anomaly(Eu=0.58–0.89). Whole-rock geochemical data shows that the Jiangshan volcanic rocks are possibly I-type granitic rocks, even though they have some characteristics of AS-type granites due to the magma fractional crystallization and water-rock interaction. Zircon δ18 O values are 3.97‰–5.49‰(average 4.50‰), 2.90‰–5.21‰(average 4.32‰) for ignimbrite from Shangshu village section, and Shanghupeng village section, respectively. They are slightly lower than the average δ18 O values of igneous zircons in equilibrium with mantle magmas(5.3 ± 0.6‰(2σ)), the lower δ18 O value also demonstrating the presence of high temperature water-rock interactions. The ignimbrite rocks have positive εNd(t)(4.02, 3.37, 3.91, 4.74, 2.85, 4.39, totals from the three areas) and εNd(t)(in-situ zircon)(4.3–14.6, a weighted mean of 8.4; 6.6–12.7, a weighted mean of 9.0; 8.1–12.0, a weighted mean of 9.5, respectively, from the three areas). In conjunction with the trace element studies, they indicate that the source region of the Jiangshan volcanic rocks was mainly composed of juvenile lower crustal material, mixed with some mantle-sourced magma. Detailed elemental and isotopic data suggest that the Jiangshan volcanic rocks were formed in a continental arc setting. There is a series of ca. 860–830 Ma volcanic rocks formed in a back-arc extensional setting in the southern margin of the eastern Jiangnan Orogen, along the northwest side of the Jiangshan–Shaoxing suture. The first stage rift-related anorogenic magmatism may have occurred as early as ca. 860 Ma in the eastern Jiangnan Orogen.  相似文献   

20.
ABSTRACT

This contribution presents new SIMS zircon U–Pb geochronology, major and trace element geochemistry, and zircon Hf–O isotope systematic on an example of Late Carboniferous granodiorite and porphyritic granodiorite intrusions from the Chihu area of Eastern Tianshan, Xinjiang. SIMS zircon U–Pb dating indicates that the Chihu granodiorite and porphyritic granodiorite formed at 320.2 ± 2.4 Ma and 314.5 ± 2.5 Ma, respectively. These rocks are metaluminous to weakly peraluminous with an A/CNK value of 0.92–1.58, as well as low 10000 Ga/Al, Zr + Nb + Y + Ce, and Fe2O3T/MgO values, which suggest an I-type normal island arc magmatic suite. The porphyritic granodiorite has a slightly higher Sr/Y ratio (28–37) and lower Y (6.9–11.7 ppm) and Yb (0.98–1.49 ppm) contents, suggesting mild adakite affinities. In situ Hf–O isotopic analyses using LA-ICP-MS-MC and SIMS indicate that the εHf(t) and δ18O values of granodiorite zircons vary from +11.5 to +14.9 and 4.80 to 5.85 ‰, respectively, similar to values for porphyritic granodiorite zircons, which vary from +11.9 to +17.2 and 3.78 to 4.71 ‰, respectively. The geochemical and isotopic data imply that the Chihu granodiorite and porphyritic granodiorite share a common origin, most likely derived from partial melts of the subduction-modified mantle. Based on the regional geological history, geochemistry of the Chihu intrusions, and new isotopic studies, we suggest that the Late Carboniferous magma was generated during the period of the northward subduction of the Palaeo-Tianshan ocean plate beneath the Dananhu–Tousuquan island arc.  相似文献   

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