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1.
The low‐Sr content (generally < 100 μg g?1) in clinopyroxene from peridotite makes accurate Sr isotopic determination by LA‐MC‐ICP‐MS a challenge. The effects of adding N2 to the sample gas and using a guard electrode (GE) on instrumental sensitivity for Sr isotopic determination by LA‐MC‐ICP‐MS were investigated. Results revealed no significant sensitivity enhancement of Sr by adding N2 to the ICP. Although using a GE led to a two‐fold sensitivity enhancement, it significantly increased the yield of polyatomic ion interferences of Ca‐related ions and TiAr+ on Sr isotopes. Applying the method established in this work, 87Sr/86Sr ratios (Rb/Sr < 0.14) of natural clinopyroxene from mantle and silicate glasses were accurately measured with similar measurement repeatability (0.0009–0.00006, 2SE) to previous studies but using a smaller spot size of 120 μm and low‐to‐moderate Sr content (30–518 μg g?1). The measurement reproducibility was 0.0004 (2s, n = 33) for a sample with 100 μg g?1 Sr. Destruction of the crystal structure by sample fusion showed no effect on Sr isotopic determination. Synthesised glasses with major element compositions similar to natural clinopyroxene have the potential to be adopted as reference materials for Sr isotopic determination by LA‐MC‐ICP‐MS.  相似文献   

2.
A new natural rutile reference material is presented, suitable for U‐Pb dating and Zr‐in‐rutile thermometry by microbeam methods. U‐Pb dating of rutile R632 using laser ablation ICP‐MS with both magnetic sector field and quadrupole instruments as well as isotope dilution‐thermal ionisation mass spectrometry yielded a concordia age of 496 ± 2 Ma. The high U content (> 300 μg g?1) enabled measurement of high‐precision U‐Pb ages despite its young age. The sample was found to have a Zr content of 4294 ± 196 μg g?1, which makes it an excellent complementary reference material for Zr‐in‐rutile thermometry. Individual rutile grains have homogeneous compositions of a number of other trace elements including V, Cr, Fe, Nb, Mo, Sn, Sb, Hf, Ta and W. This newly characterised material significantly expands the range of available rutile reference materials relevant for age and temperature determinations.  相似文献   

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

4.
The Indosinian post-collisional Wulong pluton intruded into the Mesoproterozoic Fuping Group, South Qinling, central China. In the southern part of the pluton, some mafic enclaves have sharp or gradational contact relationships with the host biotite granodiorite. Geochemistry, zircon LA-ICP MS （laser ablation inductively-coupled plasma mass spectrometry） U-Pb chronology and Sr- Nd-Pb isotope geochemistry of the pluton are reported in this paper. The biotite granodiorite shows close compositional similarities to high-silica adakite. Its chondrite-normalized REE patterns are characterized by strong HREE depletion （Yb = 0.33--0.96 10-6 and Y = 4.77-11.19 ×10^-6）, enrichment of Ba （775-1386 x 10-6） and Sr （643-1115 × 10^-6） and high Sr/Y （57.83-159.99） and Y/Yb （10.99-14.32） ratios, as well as insignificant Eu anomalies （6Eu = 0.70-0.83）, suggesting a feldspar-poor, garnet±amphibole-rich residual mineral assemblage. The mafic enclaves have higher MgO （4.15- 8.13%）, Cr （14.79-371.31 × 10-6）, Ni （20.00-224.24× 10^-6） and Nb/Ta （15.42-21.91） than the host granodiorite, implying that they are mantle-derived and might represent underplated mafic magma. Zircon LA-ICP MS dating of the granodiorite yields a ^206pb/^238U weighted mean age of 208±2 Ma （MSWD=0.50, 1σ）, which is the age of emplacement of the host biotite granodiorite. This age indicates that the Wulong pluton formed during the late-orogenic or post-collisional stage （〈242±21 Ma） of the South Qinling belt. The host biotite granodiorite displays ^87Sr/^86Sr = 0.7059-0.7062, Isr = 0.7044-- 0.7050,^143Nd/^144Nd = 0.51236-0.51238, εNd（t）= -2.26 to -2.66 to ^206Pb/^204pb = 18.099-18.209, ^207pb/^204pb = 15.873-15.979 and ^208pb/^204pb = 38.973-39.430. Those ratios are similar to those of the Mesoproterozoic Yaolinghe Group in the South Qinling. Furthermore, its Nd isotopic model age （-1.02 Ga） is consistent with the age （-1.1 Ga） of the Yaolinghe Group. Based on the integrated geological and ge  相似文献   

5.
Experimental determination of the pressure and temperature controls on Ti solubility in quartz provides a calibration of the Ti‐in‐quartz (TitaniQ) geothermometer applicable to geological conditions up to ~ 20 kbar. We present a new method for determining 48Ti mass fractions in quartz by LA‐ICP‐MS at the 1 μg g?1 level, relevant to quartz in HP‐LT terranes. We suggest that natural quartz such as the low‐CL rims of the Bishop Tuff quartz (determined by EPMA; 41 ± 2 μg g?1 Ti, 2s) is more suitable than NIST reference glasses as a reference material for low Ti mass fractions because matrix effects are limited, Ca isobaric interferences are avoided, and polyatomic interferences at mass 48 are insignificant, thus allowing for the use of 48Ti as a normalising mass. Average titanium mass fraction from thirty‐three analyses of low temperature quartz from the Czech Erzgebirge is 0.9 ± 0.2 μg g?1 (2s) using 48Ti as a normalising mass and Bishop Tuff quartz rims as a reference material. The 2s average analytical uncertainty for individual analyses of 48Ti is 8% for 50 μm spots and 7% for 100 μm spots, which offers much greater accuracy than the 21–41% uncertainty (2s) incurred from using 49Ti as an analyte.  相似文献   

6.
A natural smoky quartz crystal from Shandong province, China, was characterised by laser ablation ICP‐MS, electron probe microanalysis (EPMA) and solution ICP‐MS to determine the concentration of twenty‐four trace and ultra trace elements. Our main focus was on Ti quantification because of the increased use of this element for titanium‐in‐quartz (TitaniQ) thermobarometry. Pieces of a uniform growth zone of 9 mm thickness within the quartz crystal were analysed in four different LA‐ICP‐MS laboratories, three EPMA laboratories and one solution‐ICP‐MS laboratory. The results reveal reproducible concentrations of Ti (57 ± 4 μg g?1), Al (154 ± 15 μg g?1), Li (30 ± 2 μg g?1), Fe (2.2 ± 0.3 μg g?1), Mn (0.34 ± 0.04 μg g?1), Ge (1.7 ± 0.2 μg g?1) and Ga (0.020 ± 0.002 μg g?1) and detectable, but less reproducible, concentrations of Be, B, Na, Cu, Zr, Sn and Pb. Concentrations of K, Ca, Sr, Mo, Ag, Sb, Ba and Au were below the limits of detection of all three techniques. The uncertainties on the average concentration determinations by multiple techniques and laboratories for Ti, Al, Li, Fe, Mn, Ga and Ge are low; hence, this quartz can serve as a reference material or a secondary reference material for microanalytical applications involving the quantification of trace elements in quartz.  相似文献   

7.
Halogen contents for the widely distributed reference glasses BHVO‐2G, BIR‐1G, BCR‐2G, GSD‐1G, GSE‐1G, NIST SRM 610 and NIST SRM 612 were investigated by pyrohydrolysis combined with ion chromatography, total reflection X‐ray fluorescence analysis, instrumental neutron activation analysis, the noble gas method, electron probe microanalysis and laser ablation‐inductively coupled plasma‐mass spectrometry. Glasses BHVO‐2G, GSD‐1G and GSE‐1G have halogen contents that can be reproduced at the 15% level by all bulk techniques and cover a significant range in halogen mass fractions for F (~ 20–300 μg g?1), Cl (~ 70–1220 μg g?1) and Br (~ 0.2–285 μg g?1) and I (~ 9–3560 ng g?1). The BIR‐1G glass has low F (< 15 μg g?1), Cl (~ 20 μg g?1), Br (15 ng g?1) and I (3 ng g?1). The halogen contents for the silica‐rich NIST SRM 610 and 612 glasses were poorly reproduced by the different techniques. The relatively high Cl, Br and I abundances in glasses GSD‐1G and GSE‐1G mean that these glasses are well suited for calibrating spatially resolved micro‐analytical studies on silicate glasses, melt and fluid inclusions. Combined EPMA and laser ablation‐inductively coupled plasma‐mass spectrometry data for glass GSE‐1G demonstrate homogeneity at the 10% level for Cl and Br.  相似文献   

8.
We report homogeneity tests on large natural apatite crystals to evaluate their potential as U reference materials for apatite fission‐track (AFT) thermochronology by laser ablation‐inductively coupled plasma‐mass spectrometry (LA‐ICP‐MS). The homogeneity tests include the measurements of major element concentrations by electron probe microanalysis (EPMA), whereas for U concentration, isotope dilution (ID) ICP‐MS and laser ablation (LA) ICP‐MS were employed. Two apatite crystals are potential reference materials for LA‐ICP‐MS analysis: a 1 cm3 fraction of a Durango crystal (7.5 μg g?1 U) and a 1 cm3 Mud Tank crystal (6.9 μg g?1 U). The relative standard deviation (1 RSD) of the U concentration determined by ID‐ICP‐MS of both apatite crystals was ≤ 1.5%, whereas 1 RSD for the LA‐ICP‐MS results was better than 4%, providing sufficient homogeneity for fission‐track dating. The results on the U homogeneity for two different apatite samples are an important step towards establishing in situ dating routines for AFT analysis by LA‐ICP‐MS.  相似文献   

9.
A potential zircon reference material (BB zircon) for laser ablation‐inductively coupled plasma‐mass spectrometry (LA‐ICP‐MS) U‐Pb geochronology and Hf isotope geochemistry is described. A batch of twenty zircon megacrysts (0.5–1.5 cm3) from Sri Lanka was studied. Within‐grain rare earth element (REE) compositions are largely homogeneous, albeit with some variation seen between fractured and homogeneous domains. Excluding fractured cathodoluminescence bright domains, the variation in U content for all analysed crystals ranged from 227 to 368 μg g?1 and the average Th/U ratios were between 0.20 and 0.47. The Hf isotope composition (0.56–0.84 g/100 g Hf) is homogeneous within and between the grains – mean 176Hf/177Hf of 0.281674 ± 0.000018 (2s). The calculated alpha dose of 0.59 × 1018 g?1 for a number of BB grains falls within the trend of previously studied, untreated zircon samples from Sri Lanka. Aliquots of the same crystal (analysed by ID‐TIMS in four different laboratories) gave consistent U‐Pb ages with excellent measurement reproducibility (0.1–0.4% RSD). Interlaboratory assessment (by LA‐ICP‐MS) from individual crystals returned results that are within uncertainty equivalent to the TIMS ages. Finally, we report on within‐ and between‐grain homogeneity of the oxygen isotope systematic of four BB crystals (13.16‰ VSMOW).  相似文献   

10.
The strong spectral interference between Br‐ and Al‐induced X‐ray lines hampers the utilisation of electron probe microanalysis (EPMA) for measuring Br mass fractions in Al‐bearing minerals and glasses. Through measuring Br‐free Al‐bearing materials, we established an EPMA method to quantify the overlap from AlKα on BrLβ, which can be expressed as a linear function of the Al2O3 content. The count rate of the BrLβ peak signal was enhanced by high beam currents and long measurement times. Application of this EPMA method to Al‐ and Br‐bearing materials, such as sodalite and scapolite, and to five experimental glasses yielded Br mass fractions (in the range of 250–4000 μg g?1) that are consistent with those measured by microbeam synchrotron X‐ray fluorescence (μ‐SXRF) spectrometry. The EPMA method has an estimated detection limit of ~ 100–300 μg g?1. We propose that this method is useful for measuring Br mass fractions (hundreds to thousands of μg g?1) in Al‐bearing minerals and glasses, including those produced in Br‐doped experiments. In addition, the natural marialitic scapolite (ON70) from Mpwapwa (Tanzania) containing homogeneously distributed high mass fractions of Br (2058 ± 56 μg g?1) and Cl (1.98 ± 0.03% m/m) is an ideal reference material for future in situ analyses.  相似文献   

11.
西藏曲水碰撞花岗岩的混合成因：来自成因矿物学证据   总被引：5，自引：3，他引：5  
西藏曲水碰撞花岗岩地处冈底斯构造-岩浆带中部,呈东西向平行雅鲁藏布缝合带分布.该岩体以花岗闪长岩、石英闪长岩为主,其次为石英二长闪长岩.岩体内普遍发育微粒镁铁质包体.对花岗闪长岩、石英闪长岩及微粒镁铁质包体的成因矿物学研究结果显示：（1）斜长石发育环带且边缘和核部偏基性,幔部酸性;（2）斜长石斑晶边缘常含有角闪石、黑云母等暗色矿物包体;（3）钾长石X射线结构分析显示自核部向边缘温度呈现逐渐升高的特点;（4）长石矿物中普遍含有较高的Cr、Ni、Co元素,明显不同于壳熔花岗岩;（5）角闪石、黑云母矿物MgO含量高于典型壳熔花岗岩;（6）包体中发育针状磷灰石和角闪石,显示为岩浆淬冷的结果.上述特征不可能用正常岩浆分异作用来解释,而更可能是壳-幔岩浆混合作用的结果.采用矿物温压计所得到的结果也符合混合后的岩浆演化特征.  相似文献   

12.
The Duolong porphyry Cu–Au deposit (5.4 Mt at 0.72% Cu, 41 t at 0.23 g/t Au) was recently discovered in the southern Qiangtang terrane, central Tibet. Here, new whole‐rock elemental and Sr–Nd–Pb isotope and zircon Hf isotopic data of syn‐ and post‐ore volcanic rocks and barren and ore‐bearing granodiorite porphyries are presented for a reconstruction of magmas associated with Cu–Au mineralization. LA–ICP–MS zircon U–Pb dating yields mean ages of 117.0 ± 2.0 and 120.9 ± 1.7 Ma for ore‐bearing granodiorite porphyry and 105.2 ± 1.3 Ma for post‐ore basaltic andesite. All the samples show high‐K calc‐alkaline compositions, with enrichment of light rare earth elements (LREE) and large ion lithophile elements (LILE: Cs and Rb) and depletion of high field strength elements (HFSE: Nb and Ti), consistent with the geochemical characteristics of arc‐type magmas. Syn‐ and post‐ore volcanic rocks show initial Sr ratios of 0.7045–0.7055, εNd(t) values of −0.8 to 3.6, (206Pb/204Pb)t ratios of 18.408–18.642, (207Pb/204Pb)t of 15.584–15.672 and positive zircon εHf(t) values of 1.3–10.5, likely suggesting they dominantly were derived from metasomatized mantle wedge and contaminated by southern Qiangtang crust. Compared to mafic volcanic rocks, barren and ore‐bearing granodiorite porphyries have relatively high initial Sr isotopic ratios (0.7054–0.7072), low εNd(t) values (−1.7 to −4.0), similar Pb and enriched zircon Hf isotopic compositions [εHf(t) of 1.5–9.7], possibly suggesting more contribution from southern Qiangtang crust. Duolong volcanic rocks and granodiorite porphyries likely formed in a continental arc setting during northward subduction of the Bangong–Nujiang ocean and evolved at the base of the lower crust by MASH (melting, assimilation, storage and homogenization) processes. Copyright © 2014 John Wiley & Sons, Ltd.  相似文献   

13.
The Mazaertag layered intrusion is located in the northwestern part of the Tarim large igneous province where several early Permian layered mafic-ultramafic intrusions host important Fe-Ti oxide deposits. The intrusion covers an area of ～0.13 km~2 and has a vertical stratigraphic thickness of at least300 m. It consists chiefly of olivine clinopyroxenite, and is cut through by the nearby mafic-ultramafic dykes. In this paper, we report new mineral chemistry data and whole-rock chemical and isotopic compositions for the Mazaertag intrusion along with whole-rock isotopic compositions for the nearby mafic dykes. The averaged compositions of cumulus olivine, clinopyroxene and intercumulus plagioclase within individual samples range from Fo_(71-73),Mg~# = 76 to 79 and An_(65-75) but they do not define sustained reversals. The observed mineral compositions are consistent with the differentiation of a single batch of magma in a closed system. Rocks of the Mazaertag intrusion are characterized by enrichment in light REE relative to heavy REE, positive Nb and Ta anomalies and a small range of age-corrected ε_(Nd)(t)(-0.1 to +0.9) and initial ~(87)Sr/~(86)Sr values(0.7044 to 0.7068). The slightly lower ε_(Nd)(t), initial ~(206)Pb/~(204)Pb and higher initial ~(87)Sr/~(86)Sr values of the intrusion compared to those of the least contaminated dykes[ε_(Nd)(t) =+2.8 to +3.4;(~(206)Pb/~(204)Pb)_i = 18.516-18.521;(~(87)Sr/~(86)Sr)_i = 0.7038-0.7041] imply that the Mazaertag magma was subjected to small to modest degrees of contamination by the upper crust. The Sr-Nd isotopic compositions of the least contaminated dykes are consistent with derivation from a FOZO-like mantle source. The parental magma of the Mazaertag intrusion, estimated from clinopyroxene compositions using mineral-melt partition coefficients, has trace element compositions similar to some of the most primitive mafic dykes in the same area. This suggests that the Mazaertag intrusion and mafic dykes shared a similar mantle source. Therefore, the parental magma of the Mazaertag intrusion was interpreted to have originated from a mantle plume. Based on the Cr_2 O_3 contents in titanomagnetite and less-evolved characteristics of the Mazaertag intrusion compared to the Wajilitag Fe-Ti oxide deposit in Bachu, it is speculated that there might not be a potential to find economic Fe-Ti oxide mineralization in the intrusion.  相似文献   

14.
In this study, we report both 143Nd/144Nd and 147Sm/144Nd values in twelve minerals (apatite, titanite, monazite and eudialyte) based on analyses over 4 years using LA‐MC‐ICP‐MS. The positive correlation between the measured βSm and βNd (r2 = 0.9981) over this time in our laboratory demonstrates the excellent long‐term stability of the method. Compared with the normal method, Sm and Nd signal intensities were improved by a factor of 2.9 with the use of X skimmer and Jet sample cones in combination with the addition of nitrogen at 3–6 ml min?1 to the central gas flow. The enhancement of signal intensity benefits the accurate in situ determination of the Sm‐Nd isotopes of samples poor in these elements. 143Nd/144Nd values were also determined in two manganese nodules and GSMC Co‐rich crust with low mass fractions of Nd (94–293 μg g?1). Generally, most of the obtained Sm‐Nd isotopic compositions in these geological materials are consistent with published values. ‘External reproducibility’ (2s) of 143Nd/144Nd and 147Sm/144Nd was typically better than 0.06‰ and 2.5‰, respectively, demonstrating that the Durango, Otter Lake, NW‐1 and MAD apatites, the Khan, and OLT‐1 titanites, MGMH#117531 monazite and LV01 eudialyte are promising candidate reference materials for in situ Sm‐Nd isotopic determinations. The Trebilcock, Mae Klang and 44069 monazites are only suitable for in situ Nd isotopic determinations because of their heterogeneous Sm/Nd compositions. The heterogeneous Sm‐Nd composition of titanite BLR‐1 demonstrates that it is not a suitable reference material for in situ Sm‐Nd isotopic determinations. Deep‐sea samples (NOD‐A‐1 and NOD‐P‐1 manganese nodule, GSMC Co‐rich crust) with low mass fractions of Nd also show homogenous Nd isotopic compositions. Sm‐Nd isotopic ratios of a monazite (MQG‐22) from the North China Craton were measured as a case study and gave a 147Sm‐143Nd isochron age of 1792 ± 35 Ma (MSWD = 3.2) consistent with the published metamorphic age of the host metasedimentary rocks. The results for both candidate reference materials and geological samples demonstrate that the in situ LA‐MC‐ICP‐MS analytical protocol described is feasible and robust for research in geological evolution.  相似文献   

15.
杨堂礼  蒋少涌 《地球科学》2015,40(12):2002-2020
九瑞矿集区成矿与燕山期中酸性侵入岩体关系密切,但对该区东雷湾矿床的地质地球化学研究还相对较少.对东雷湾矿区中酸性侵入岩(花岗闪长斑岩、石英闪长玢岩)及其铁镁质包体进行了系统的锆石U-Pb年代学、矿物化学、岩石地球化学和Sr-Nd-Pb-Hf同位素研究,探讨其岩石成因.锆石LA-ICP-MS U-Pb定年表明:东雷湾中酸性侵入岩的成岩年龄为144.3~148.7 Ma,铁镁质包体的年龄为146.4~147.1 Ma,与寄主侵入岩花岗闪长斑岩的年龄一致.东雷湾侵入岩属准铝质范围,岩石的Mg#较高(42.5~68.0,平均56.0),并具有较高的相容元素含量,富集轻稀土,Eu异常不明显,富集大离子亲石元素,亏损高场强元素.暗色铁镁质包体呈细粒结构,常见针状磷灰石和钾长石斑晶.东雷湾样品的Sr-Nd同位素组成变化范围较小,初始87Sr/86Sr比值位于0.706 4 ~ 0.707 9,εNd(t)值变化于-5.80~-3.31,t2DM(Nd)为1.2~1.4 Ga,锆石εHf(t)值为-15.9~-3.6.样品的206Pb/204Pb(t)、207Pb/204Pb(t)、208Pb/204Pb(t)值分别变化于17.333 3~18.260 0、15.513 5~15.621 0、37.404 1~38.395 4之间.详尽的元素和同位素地球化学特征表明,东雷湾铁镁质包体是由拆沉的加厚下地壳发生部分熔融,并在其上升过程中与地幔物质发生相互作用,进而与花岗质岩浆混合过冷结晶形成的.该区侵入岩的形成很可能是因为加厚下地壳拆沉入软流圈地幔后发生部分熔融,熔体与地幔橄榄岩相互作用后在上侵的过程分别形成了铁镁质岩石和花岗质岩石.   相似文献   

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

17.
陈兵  熊富浩  马昌前  陈越  黄虎 《地球科学》2021,46(6):2057-2072
壳-幔岩浆相互作用如何影响长英质火成岩的岩石学多样性是当前岩石学研究的焦点问题之一.以岩石类型丰富的东昆仑白日其利长英质岩体和暗色微粒包体为研究对象,开展系统的锆石U-Pb年代学、矿物学、全岩元素地球化学和Sr-Nd-Hf同位素研究,探讨和解析这一重要科学问题.LA-ICPMS锆石U-Pb年代学研究表明,暗色微粒包体（247.8±2.0 Ma）与二长花岗岩（247.5±1.4 Ma）、花岗闪长岩（248.8±2.1 Ma）和石英闪长岩（248.8±1.5 Ma）均侵位结晶于早三叠世.岩相学和矿物学研究表明,白日其利长英质岩石与包体的成因机制与壳-幔岩浆的机械或化学混合作用密切相关.元素地球化学和Sr-Nd-Hf同位素组成研究揭示,幔源镁铁质岩浆端元起源于受俯冲板片流体交代的富集地幔熔融,而壳源长英质岩浆端元则起源于东昆仑古老的变质杂砂岩基底.岩石成因分析揭示,幔源镁铁质岩浆侵入长英质晶粥岩浆房,促使长英质晶粥发生活化,随后壳-幔岩浆端元以不同比例和不同方式发生机械和化学混合等相互作用,从而形成镁铁质岩墙、包体、石英闪长岩和花岗闪长岩等多种岩石类型.晶粥状态下壳-幔岩浆相互作用是控制东昆仑长英质火成岩多样性和大陆地壳生长演化的重要方式.   相似文献   

18.
The Yangla copper deposit, located in western Yunnan Province, China, is a typical giant, newly started mining copper deposit with an estimated Cu reserves of about 1,200,000 tons. The deposit is spatially and temporally associated with the Linong granodiorite, which is rich in SiO2 (SiO2=58.25 wt%–69.84 wt%) and alkalis (Na2O+K2O=5.98 wt%–8.34 wt%), indicating an association with shoshonitic series to high-K calc-alkaline series granites, and shows low contents of TiO2 (0.35 wt%–0.48 wt%), MgO (1.51 wt%–1.72 wt%), and Al2O3 (13.38 wt%–19.75 wt%). The δ34S values of sulfides of the main ore stage from copper ores vary range from ?4.2‰ to ?0.9‰, indicating a much greater contribution from the mantle to the ore-forming fluids. The δ34S values of the late ore stage is ?9.8‰, indicating enrichment of biogenic sulfur which may derive from the crustal hydrothermal fluid. The 208Pb/204Pb, 207Pb/204Pb and 206Pb/204Pb of sulfides of the main ore stage from copper ores range within 38.66–38.73, 15.71–15.74 and 18.35–19.04, respectively, implying that the Pb was derived from the mantle, with the crustal component, probably representing mixtures of mantle lead and crustal lead. Sulfide of the late ore stage in their Pb isotopic composition, 208Pb/204Pb= 38.69, 207Pb/204Pb=15.70, 206Pb/204Pb=18.35, implying that the Pb was derived from the crust. The Linong granodiorite is syn-collisional, produced by partial melting of thickened lower crust, which was triggered by the westward subduction of the Jinshajiang Oceanic plate. During a transition in geodynamic setting from collision-related compression to extension, gently dipping ductile shear zones (related to subduction) were transformed to brittle shear zones, consisting of a series of thrust faults in the Jinshajiang tectonic belt. The tensional thrust faults would have been a favorable environment for ore-forming fluids. The ascending magma provided a channel for the ore-forming fluid from the mantle wedge. After the magma arrived at the base of the early-stage Linong granodiorite, the platy granodiorite at the base of the body would have shielded the late-stage magma from the fluid. The magma would have cooled slowly, and some of the ore-forming fluid in the magma would have entered the gently dipping thrust faults near the Linong granodiorite, resulting in mineralization.  相似文献   

19.
The major and trace elements and Sr–Nd–Pb isotopes of the host rocks and the mafic microgranular enclaves (MME) gathered from the Dölek and Sariçiçek plutons, Eastern Turkey, were studied to understand the underlying petrogenesis and geodynamic setting. The plutons were emplaced at  43 Ma at shallow depths ( 5 to 9 km) as estimated from Al-in hornblende geobarometry. The host rocks consist of a variety of rock types ranging from diorite to granite (SiO2 = 56.98–72.67 wt.%; Mg# = 36.8–50.0) populated by MMEs of gabbroic diorite to monzodiorite in composition (SiO2 = 53.21–60.94 wt.%; Mg# = 44.4–53.5). All the rocks show a high-K calc-alkaline differentiation trend. Chondrite-normalized REE patterns are moderately fractionated and relatively flat [(La/Yb)N = 5.11 to 8.51]. They display small negative Eu anomalies (Eu/Eu = 0.62 to 0.88), with enrichment of LILE and depletion of HFSE. Initial Nd–Sr isotopic compositions for the host rocks are εNd(43 Ma) = − 0.6 to 0.8 and mostly ISr = 0.70482–0.70548. The Nd model ages (TDM) vary from 0.84 to 0.99 Ga. The Pb isotopic ratios are (206Pb/204Pb) = 18.60–18.65, (207Pb/204Pb) = 15.61–15.66 and (208Pb/204Pb) = 38.69–38.85. Compared with the host rocks, the MMEs are relatively homogeneous in isotopic composition, with ISr ranging from 0.70485 to 0.70517, εNd(43 Ma) − 0.1 to 0.8 and with Pb isotopic ratios of (206Pb/204Pb) = 18.58–18.64, (207Pb/204Pb) = 15.60–15.66 and (208Pb/204Pb) = 38.64–38.77. The MMEs have TDM ranging from 0.86 to 1.36 Ga. The geochemical and isotopic similarities between the MMEs and their host rocks indicate that the enclaves are of mixed origin and are most probably formed by the interaction between the lower crust- and mantle-derived magmas. All the geochemical data, in conjunction with the geodynamic evidence, suggest that a basic magma derived from an enriched subcontinental lithospheric mantle, probably triggered by the upwelling of the asthenophere, and interacted with a crustal melt that originated from the dehydration melting of the mafic lower crust at deep crustal levels. Modeling based on the Sr–Nd isotope data indicates that  77–83% of the subcontinental lithospheric mantle involved in the genesis. Consequently, the interaction process played an important role in the genesis of the hybrid granitoid bodies, which subsequently underwent a fractional crystallization process along with minor amounts of crustal assimilation, en route to the upper crustal levels generating a wide variety of rock types ranging from diorite to granite in an extensional regime.  相似文献   

20.
U-Pb zircon age, geochemical, and Sr-Nd-Pb isotopic data of mafic dykes from eastern Shandong Province, eastern China is reported herein. Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) U-Pb zircon analyses of two samples from the investigated mafic dykes yield consistent ages ranging from 121.9 Ma ± 0.47 Ma to 122.9 Ma ± 0.61 Ma. The mafic dykes are characterized by high (87Sr/86Sr) i ranging from 0.7087 to 0.7089, low εNd(t) values ranging from -16.9 to -17.8, 206Pb/204Pb = 17.15 to 17.17, 207Pb/204Pb = 15.45 to 15.47, and 208Pb/204Pb = 37.59 to 37.68. Results from the current study suggest that the mafic dykes are derived from partial melting of ancient lithospheric mantle that was variably hybridized by melts derived from foundered lower crustal eclogite. The mafic dykes may have been generated through subsequent insignificant crystal fractionation and very minor crustal contamination during magma ascent. Combined with previous studies, the current findings provide new evidence that the intense lithospheric thinning beneath the eastern Shandong Province of eastern China occurred at ~120 Ma, and that this condition was caused by the removal of the lower lithosphere (mantle and lower crust).  相似文献   

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