A ca. 2.2Ga Acidic Magmatic Event at the Northern Margin of the Yangtze Craton: Evidence from U-Pb Dating and Hf Isotope Analysis of Zircons from the Kongling Complex

Objective The Yangtze craton collisional orogeny at ca. extensional events at ca. 1 experienced Paleoproterozoic 1.95-2.0 Ga and post-orogenic 85 Ga related to amalgamation of the Columbia （Nuna） supercontinent （Zhao and Cawood, 2012）. A ca. 2.15 Ga suprasubduction zone ophiolitic melange was recongized in the Archean- Paleoproterozoic Kongling Complex of the northern Yangtze craton （Han et al., 2017）. However, the tectonic evolution in early Paleoproterozoic from 2.4 Ga to 2.2 Ga remains unclear. We report here the presence of a suite of Paleoproterozoic （2.2 Ga） granites in the Huangling dome, northern Yangtze craton, which may provide important insights into crustal growth processes in the craton prior to the assembly of Columbia.

Determination of Carbon and Nitrogen Isotope Fractions in Asparagine, Aspartic Acid, Threonine and Methionine

The nomenclature for compounds that are modified with isotopes is growing every day. Compounds can be modified with isotopes either individually, in a functional group or groups, or completely with all atomic centers of the element. This diversity of isotope-modified compounds increases the range of researches that can be studied using them. Compounds modified with isotopes of carbon-13 or nitrogen-15 can be converted into carbon monoxide, carbon dioxide and molecular nitrogen. Currently, only the average value of carbon-13 or nitrogen-15 isotopes can be determined. However, by directly determining the atomic share of these isotopes in organic compounds modified with isotopes, information about the isotopic centers of the element can be obtained. The atomic fraction of an element is defined as a single carbon or nitrogen isotope-modified center or centers, or all centers that are isotope-modified with that element at the same time. Carbon-13 or nitrogen-15 isotopes’ atomic fraction can be determined molecularly or with fragment ions of different elemental content, or both. This makes the method self-verifying, increasing the accuracy and reliability of the results obtained. Amino acids, such as asparagine, aspartic acid, methionine, and threonine, are essential for the human body. This proposed method of isotopic analysis will increase the possibilities for scientific research using these compounds.

Recent applications of isotope analysis to forensic anthropology

Isotope analysis has become an increasingly valuable tool in forensic anthropology case-work over the past decade. Modern-day isotopic investigations on human remains have integrated the use of multi-isotope profiles (e.g. C, N, O, H, S, Sr, and Pb) as well as iso-topic landscapes ("isoscapes") from multiple body tissues (e.g. teeth, bone, hair, and nails) to predict possible region-of-origin of unidentified human remains. Together, data from various isotope analyses provide additional lines of evidence for human identification, including a decedent's possible region-of-birth, long-term adult residence, recent travel history, and dietary choices. Here, we present the basic principles of isotope analysis and provide a brief overview of instrumentation, analytical standards, sample selection, and sample quality measures. Finally, we present case studies that reflect the diverse applications of isotope analysis to the medicolegal system before describing some future research directions. As shown herein, isotope analysis is a flexible and powerful geolocation tool that can provide new investigative leads for unidentified human remains cases.

Carbon Oxygen Isotope Analysis and Its Significance of Carbonate in the Zhaogezhuang Section of Early Ordovician in Tangshan,North China

In the Early Ordovician Zhaogezhuang Section of Tangshan , North China, the Yeli Formation is composed of an entire third-order sequence, with facies ranging from the inner ramp restricted platform and open marine to the middle and even outer ramps. The Liangjiashan Formation is dominated by highstand system tracts （HST） with predominantly inner ramp grain-shoal and lagoon facies. Analyzing the carbon and oxygen isotope during the whole-rock carbonate reveals the 613C values in the Yeli Formation range from -7.11%o-0.76%o （PDB）, with the mean value at -2.98%0, while the 6180 values range of-9.09%o- -4.65%o with the mean value at -6.12%o. The 613C values in the Liangjiashan Formation range of -1.15%o-0.3%o, and the mean value of -0.57%0; the 61SO values are -8.76%0- -7.48%0, and the mean value is -8.06%o. The 613C values in the Yeli Formation decrease, but at the bottom of the Liangjiashan Formation the values increase steadily. In the middle-upper formation, there is an extended fluctuation between 0- -1.00%o. The 613C trend in the studied section is similar to that of the contemporary sections, except that it has much lower 613C values and a more negative excursion. The correlation between the 613C changes and the eustatic events, as well as the sedimentary facies, indicates that in the Tangshan area, the carbon isotope evolution can be attributabled to the processes of the eutrophic sea/oligotrophic sea, the seafloor organism- mediated oxidation in shallow water and the organic reduction after maximum flooding. The changes in the carbon isotope contents were primarily affected by the regional relative sea level changes. Compared to the other coeval data, the Early Ordovician of the Tang shan area is also severely depleted in 180, with all of the 6180sample values being Delow 5%o, except for one sample with a value ot -4.02%0. Witlt the ancient sea- water having a 6180 value of-5.5%0 （SMOW）, it is reasonable to delineate a temperature of less than 37 C.

Determination of trophic levels of marine fish in the Yellow Sea and northern East China Sea using nitrogen stable isotope (δ^(15)N) analysis of otoliths

Fish otolithδ^(15) N(δ^(15) N_(oto))is a demonstrated source of information of dietary history for marine fi sh as it is available iN_(oto)lith archives and sedimentary deposits unlike white muscle tissue(WMT).WMT and stomach content data are insufficient for trophic level(TL)data of past fi shes which is important for the changes of marine fi shery resources over long time scales.To determine the correlation betweenδ^(15) N_(oto) and fi sh WMTδ^(15) N(δ^(15) N_(wmt))and the feasibility of usingδ^(15) N_(oto) in characterizing the TLs of marine fi shes,we conducted nitrogen stable isotope analysis(SIA)in the otolith and WMT of 36 marine fi sh species sampled from the Yellow Sea and northern East China Sea in 2011-2014.Bothδ^(15) N_(oto) andδ^(15) N_(wmt) were analyzed using an elemental analyzer coupled with an isotope ratio mass spectrometer(EA-IRMS).Multiple otoliths were combined to make each otolith measurement and were analyzed as-is without a carbonate dissolution pre-processing step.δ^(15) N_(oto) andδ^(15) N_(wmt) comparisons for species in the Yellow Sea and northern East China Sea are currently lacking and would be helpful for both regional studies and for increasing the number of species for whichδ^(15) N_(oto) andδ^(15) N_(wmt) have been compared.Additionally,to determine the relative accuracy of trophic level calculated usingδ^(15) N_(oto),we compared TL calculated fromδ^(15) N_(oto) to traditional trophic level metrics calculated usingδ^(15) N_(wmt).The results showed a positive and highly signifi cant correlation(R=0.780,P<0.001)betweenδ^(15) N_(oto) andδ^(15) N_(wmt).Trophic level estimation using WMT(TL wmt)and otolith(TL oto)showed congruence in our study,which is not entirely surprising given thatδ^(15) N_(oto) was regressed againstδ^(15) N_(wmt) and the resulting regression coefficient was used to convertδ^(15) N_(oto) toδ^(15) N_(wmt) prior to calculating TL oto.This conversion was required in order to be consistent with previousδ^(15) N_(wmt)-based calculations of TL for comparison.TL oto calculations resulted in TL values that were largely within 5%-10%of TL values calculated withδ^(15) N_(wmt).Our fi ndings show thatδ^(15) N_(oto) is a feasible technique for characterizing the TLs of marine fi sh and can also assist in food web and marine ecosystem studies.

Isotopic analysis based on terahertz spectrum

As a new promising detection technology in the terahertz research field,the terahertz time-domain spec-troscopy(THz-TDS)has very broad application potential in many fields because its advantage on the characteristic spectrum,wide spectrum and non-destructive analysis of interested substances.In this paper,the terahertz absorption spectra of gases mixed with 12 CO and 13 CO in the spec-trum range of 0.5–2.5 THz are measured by terahertz time-domain spectroscopy for the first time.Several isotopo-logues can be clearly distinguished based on the difference in their rotational energies and the consequent terahertz spectrum.The experimental results show that 12 CO and 13 CO have obvious characteristic absorption peaks in the spectrum range of 0.5–2.5 THz due to the difference in rotational energy,and the rotational constant B can be calculated according to the experimental values to distin-guish the two gaseous isotopologues.The frequency posi-tions of the characteristic absorption peak measured by this experiment and the rotation constant B calculated accord-ing to the experimental values are compared with those previous theoretical calculations and experimental results,and they are in good agreement.This result lays a foun-dation for developing more sophisticated terahertz instru-ments to the detection of different isotopologues.

Stable Isotope Dilution Analysis of Gibberellin Residues in Tomato Paste by Liquid Chromatography-Tandem Mass Spectrometry

An accurate and sensitive method for the simultaneous determination of gibberellic acid（GA3）, gibberellin A4（GA4） and gibberellin A7（GA7） residues in tomato paste was developed by coupling solid phase extraction to high performance liquid chromatography-tandem mass spectrometry（LC-MS/MS） with electrospray ionization based stable isotope dilution analysis（SIDA）. The isotope labeled internal standard can compensate for the losses during the extraction and cleanup steps and for discrimination due to ion suppression. After extraction from methanol, hydrophile lipophilic balance（HLB） solid phase extraction（SPE） column was tested for the capacity of the cleanup of the tomato paste in compared with C18 SPE column which is the common way to the detection of GAs, and the former gained better result. Spiked experiments were performed in the non-contaminated tomato pastes and the recoveries of GA3, GA4 and GA7 were 42.6%―75.0% in external standard method（ESM） and 91.1%―103.8% in internal standard method（ISM） respectively. The validities of this method were investigated and good analytical performance for the three GAs was obtained, including low limits of method detection（2 ng/g for GA3 and GA4, 0.3 ng/g for GA7）, excellent linear dynamic ranges（5―500 ng/g for GA3 and GA4, 1―100 ng/g for GA7） and good relative standard deviation ranges（4.8%―9.4% for the intra-day test and 3.5%―11.9% for the inter-day test）.

Effects of pretreatment procedures on fatty acid composition and stable carbon isotopes in the marine microalga Isochrysis zhanjiangenisis

This study aims to quantify the effects of different pretreatment methods on the stable carbon isotope values of fatty acids in marine microalgae（Isochrysis zhanjiangenisis）.To identify the effects of sample preparation on theδ^（13）C value and the fatty acid composition,we examined eight types of pretreatment methods including：（a） drying the sample followed by direct methyl esterification using HCl-CH3OH;（b） drying the sample followed by direct methyl esterification using H2SO4-CH3OH;（c） drying the sample by ultrasonic extraction and methylesterification using HCl-CH3OH;（d） drying the sample by ultrasonic extraction and methyl-esterification using H2SO4-CH3OH;（e） fresh sample followed by direct methyl-esterification using HCl-CH3OH;（f） fresh sample followed by direct methyl-esterification using H2SO4-CH3OH;（g） fresh sample with ultrasonic extraction followed by methyl-esterification using HCl-CH3OH,and（h） fresh sample with ultrasonic extraction followed by methylesterification using H2SO4-CH3 OH.The results show that the δ^（13）C values from Groups a-e,g and h fluctuated within 0.3‰,and the δ^（13）C values of Group f were approximately 0.7‰ lower than the other seven groups.Therefore,the different sample pretreatment methods used towards the extraction of fatty acids from marine microalgae may result in different results regarding the stable carbon isotope ratios,and if necessary a correction should be applied.

SHRIMP zircon dating and LA-ICPMS Hf analysis of early Precambrian rocks from drill holes into the basement beneath the Central Hebei Basin,North China Craton

The Central Hebei Basin （CHB） is one of the largest sedimentary basins in the North China Craton, extending in a northeast-southwest direction with an area of 〉350 km2. We carried out SHRIMP zircon dating, Hf-in-zircon isotopic analysis and a whole-rock geochemical study on igneous and metasedi- mentary rocks recovered from drill holes that penetrated into the basement of the CHB, Two samples of gneissic granodiorite （XG1-1） and gneissic quartz diorite 048-1） have magmatic ages of 2500 and 2496 Ma, respectively. Their zircons also record metamorphic ages of 2.41-2.51 and ～2.5 Ga, respec- tively. Compared with the gneissic granodiorite, the gneissic quartz diorite has higher REE contents and lower Eu/Eu＊ and （La/Yb）n values. Two metasedimentary samples （MG1, H5） mainly contain ～2,5 Ga detrital zircons as well as late Paleoproterozoic metamorphic grains. The zircons of different origins have eHf （2.5 Ga） values and Hf crustal model ages ranging from 0 to 5 and 2.7 to 2,9 Ga, respectively, Therefore, ～2.5 Ga magmatic and Paleoproterozoic metasedimentary rocks and late Neoarchean to early Paleoproterozoic and late Paleoproterozoic tectono-thermal events have been identified in the basement beneath the CHB. Based on regional comparisons, we conclude that the early Precambrian basement beneath the CHB is part of the North China Craton.

Isotopic analysis of the snow cover at an alpine glacier as an indicator of local climatic variations and isotopic homogenization processes

Stratigraphic variations of 18 O/ 16 O ratios of winter accumulated snow at an alpine temperate glacier correspond to temporal patterns of local climatic variations. Although the snow is influenced by percolation and homogenization processes, the isotope stratigraphy in the glacier's accumulation area is not destroyed during the first part of summer. Below the equilibrium line altitude, rapid melting results in isotopic homogenization. Variation of δ 18 O values in the firn are relatively small.

A warmer but drier Marine Isotope Stage 11 during the past 650 ka as revealed by the thickest loess on the western Chinese Loess Plateau

Marine Isotope Stage 11（MIS 11; ca. 423-362 ka） is generally considered to be the best analogue for the present interglacial（Holocene）, and investigation of it will improve our understanding of current climate variability and assist in predictions of future climate change. However, many recent studies primarily focus on the structure and duration of MIS 11. Little research has focused on climate warmth and stability recorded in the Chinese loess-paleosol sequences（LPS） during the S4 paleosol formation（equivalent to MIS 11）. On the basis of previous work, this study presents a high-resolution record（ca. 75 a/cm） that spans from MIS 1 to MIS 15, as preserved in the thickest known Jingyuan loess section on the western Chinese Loess Plateau（CLP）. This LPS is almost 165 m thick and was sampled from the upper part of L6 to the modern soil at 2-cm depth intervals. Measurements of magnetic susceptibility, mean grain size and ＆gt;63 μm particle content, carbonate content, total organic carbon, and soil color of samples were made to reconstruct the paleoclimate variation, and a grain-size age model was used to constrain the chronological framework. The primary results show that a generally warm-humid climate dominated the S4 paleosol development, but the climate condition was extremely unstable during the whole of MIS 11. Two obviously different climate regimes controlled the MIS 11 climate variation： the early part of MIS 11 was extremely warm and stable, but the latter part was relatively cool（non-glacial） and unstable. This climate pattern was consistent with records on the central CLP and wavelet analysis suggested that it was forced by the 65°N insolation variability modulated by a quasi-100-ka cycle. In addition, a multi-proxy comparative study on the climate conditions during S0 to S5 paleosol development indicates that the period of S4 development might be the warmest interglacial of the past 650 ka. However, the climate condition during S4 development was not the most humid episode as recorded in Xifeng and Luochuan loess sections on the central CLP. On the contrary, it was drier than both the MIS 15 and the present interglacial on the western CLP, which is somewhat similar to the present climate pattern on the central CLP.

Melt extraction and mineralization: A case study from the Shuangjianzishan supergiant Ag-Pb-Zn deposit(208 Mt), Inner Mongolia, NE China

The supergiant Shuangjianzishan(SJZ) Ag-Pb-Zn deposit is in the southern segment of the Great Hinggan Range(SGHR), northeast China. Previous studies suggest the ore-forming material and fluid originated from the magmatic system, and the mineralization age was consistent with the diagenetic age. However,the relationship between granitic magmatism and mineralization is still unclear in the SJZ. In this study, CH-O-He-Ar and in-situ S-Pb isotope analyses were conducted to determine the sources of ore-forming fluids and metals, which were combined with geochemistry data of SJZ granitoids from previous studies to constrain the relationship between the magmatism and the mineralization. The C-H-O-He-Ar-S-Pb isotopic compositions suggested the SJZ ore-forming material and fluids were derived from a magmatic source, which has mixed a small amount of mantle-derived materials. In addition, the disseminated sulfide from the syenogranite has comparable S-Pb isotopic composition with the sulfide minerals from ore veins,suggesting that the generation of the SJZ ore-forming fluids has a close relationship with the syenogranite magmatism. Combining with the geochemical characters of the syenogranite, the authors proposed that the mantle-derived fingerprint of the SJZ ore-forming fluid might be caused by the parent magma of the syenogranite, which was derived from partial melting of the juvenile lower crust, and underwent the residual melts segregated from a crystal mush in the shallow magma reservoir. The extraction of the syenogranite parent magma further concentrated the fertilized fluids, which was crucial to mineralization of the SJZ Ag-Pb-Zn deposit.

庙岛群岛毗邻海域秋季底栖食物网潜在碳来源贡献及对碳汇渔业的思考

陆架边缘海是全球海洋重要的碳汇区域,而近岸岛屿毗邻海域作为最具代表性的边缘海域,具有来自海洋与陆地的不同碳来源,在碳循环和海洋碳汇中发挥着重要作用。本研究基于碳氮稳定同位素方法,利用贝叶斯混合模型,分析2020年秋季庙岛群岛毗邻海域底栖食物网中不同碳来源(浮游植物、大型藻类、悬浮颗粒有机物和底质有机物)对主要消费者类群(水生底栖无脊椎动物、杂食性鱼类、底栖食性鱼类和肉食性鱼类)的相对贡献,并以此对海洋碳汇和碳汇渔业展开了讨论。结果显示,庙岛群岛毗邻海域秋季底栖食物网生物类群的潜在碳来源主要为藻类(包括浮游植物和大型藻类)和海底底质有机质(SOM),但悬浮颗粒有机物(POM)的贡献较低。碳来源主要以内源性碳(海源)为主。由于大型藻类对水生底栖无脊椎动物的贡献明显高于鱼类,在碳汇渔业的指导下,合理科学地进行藻类增养殖,并通过贝类或以贝藻为食的鱼类混和养殖可能增加碳汇能力,从而促进碳汇渔业的发展。

Mass-Spectrometric Method of Measurement of Isotopic Content of Nitrogen in Organic Compounds

Nitrogen-15 isotope-modified compounds are widely used in medicine, pharmacology, agriculture and various fields of science and their nomenclature is gradually increasing. Their widespread use depends on the availability of inexpensive and simple isotope analysis methods. The present article is an attempt to determine the nitrogen-15 isotope content directly in organic compounds without their conversion. The general principle of possibility of determination of the isotopes of nitrogen directly in organic compounds is proposed. Based on the study of mass-spectra of Carbamide Carbonyldiamide, isocyanic acid and nitrobenzene the mass peaks are selected, by which it is possible to determine the atomic fraction of the isotopes of nitrogen. The respective formulas are proposed.

Carbon and Oxygen Isotopic Compositions: How Lacustrine Environmental Factors Respond in Northwestern and Northeastern China

Surface lake sediments, 28 from Hoh XU, 24 from northeastern China, 99 from Lake Bosten, 31 from Ulungur and 26 from Heihai were collected to determine δ13C and δ18O values. Considering the impact factors, conductivity, alkalinity, pH, TOC, C/N and carbonate-content in the sediments, CI, P, S, and metal element ratios of Mg/Ca, Sr/Ca, Fe/Mn of bulk sediments as environmental variables enable evaluation of their influences on δ13C and δ18O using principal component analysis （PCA） method. The closure and residence time of lakes can influence the correlation between δ13C and δ18O. Lake water will change from fresh to brackish with increasing reduction and eutrophication effects. Mg/Ca in the bulk sediment indicates the characteristic of residence time, Sr/Ca and Fe/Mn infer the salinity of lakes. Carbonate formation processes and types can influence the 6~3C--~1So correlation. ~180 will be heavier from Mg-calcite and aragonite formed in a high-salinity water body than calcite formed in freshwater conditions. When carbonate content is less than 30%, there is no relationship with either 613C or 6180, and also none between δ13C and δ18O. More than 30%, carbonate content, however, co-varies highly to δ13C and δ18O, and there is also a high correlation between δ13C and δ18O. Vegetation conditions and primary productivity of lakes can influence the characteristics of δ13C and δ18O, and their co-variance. Total organic matter content （TOC） in the sediments is higher with more terrestrial and submerged plants infilling. In northeastern and northwestern China, when organic matter in the lake sediments comes from endogenous floating organisms and algae, the δ13C value is high. δ13C is in the range of-4‰ to 0‰ when organic matter comes mainly from floating organisms （C/N〈6）; in the range of-4‰ to 8‰ when organic matter comes from diatoms （C/N=6 to 8）; and -8‰ to -4‰ when organic matter comes from aquatic and terrestrial plants （C/N〉8）.

Hydrocarbon test in lower-layer atmosphere to predict deep-sea petroleum or hydrate in the Okinawa Trough: an example

Light hydrocarbon (methane, ethane, propane, butane and CO2) test and C isotopic analysis of CO are conducted for over 100 lower-layer atmospheric samples from the East China Sea slope and the Okinawa Trough. The results show that the lower-layer atmosphere mainly consists of CO2 and then of CH4, and the CO2 concentrations are calculated to have a high average value of 0.87 omega/10(-2) about three times that of the regional background (0-3 omega/10(-2)). The result also shows that the average value of C isotope - 20.8 x 10(-3) is given to the CO2, inferring that it is inorganic gas. Thus, for the future 's work in the Okinawa Trough, special attention should be paid to CO2 hydrate, which is very possibly an important hydrate type.

Metallurgy at the Crossroads: New Analyses of Copper-based Objects at Tianshanbeilu, Eastern Xinjiang, China

Tianshanbeilu is the largest Bronze Age site in eastern Xinjiang, China. Stretching across the entire second millennium BC, it performed a prominent role in connecting the Hexi corridor, Central China and the steppe. A further insight into the metallurgical tradition and the metal supply network is of vital importance to improve our understanding of its multi-connected nature. This paper offers a new set of chemical and isotopic data on the copper-based objects at Tianshanbeilu, including alloying elements, trace elements(impurities) and lead isotopes. Combining the concentrations of arsenic and antimony reveals that arsenic was introduced to copper partially due to the use of specific minerals tethrahedrite-tennantite. Lead isotopes demonstrate that multiple sources of copper were employed at Tianshanbeilu and a majority of them are characterized by common lead, which appears rather different from those of the Central Plains and the Hexi corridor, but highly consistent with local ores. Surprisingly, one object at Tianshanbeilu contains the well-known highly radiogenic lead. This object undoubtedly marks the westernmost boundary of the distribution of the highly radiogenic lead. We also anticipate that more lead isotopic analyses in NW China will further contribute to the study of the highly radiogenic lead in Central China.

Developing an authentication approach using SPME-GC-IRMS based on compound-specific δ^(13)C analysis of six typical volatiles in wine

An analytical method using gas chromatography isotope ratio mass spectrometry(GC-IRMS)combined with solid phase micro-extraction(SPME)was developed to measure the 613C values of six typical volatiles commonly occurring in wine(isoamyl acetate,2-octanone,limonene,2-phenylethanol,ethyl octanoate and ethyl decanoate)for the first time.SPME selected with a divinylbenzene/carboxen/polydimethylsiloxane fiber was combined with the GC-IRMS for pretreatment optimization.The optimized SPME parameters of extraction time,extraction temperature and salt concentration were 40 min,40℃ and 10%,respectively.The 613C values measured by SPME-GC-IRMS were in good agreement with those measured via elemental analyzer(EA)-IRMS and GC-IRMS.The differences range from 0.02‰to 0.44‰ with EA-IRMS and from 0 to 0.28‰ with GC-IRMS,indicating the high accuracy of the method.This newly established method measured the precision within 0.30‰ and was successfully validated to discriminate imported real wine samples with identical label but amazing price differences from different importers.

Accurate Determination of Zr Isotopic Ratio in Zircons by Femtosecond Laser Ablation MC-ICP-MS with “Wet” Plasma Technique

This work evaluates the use of femtosecond laser ablation multiple collector inductively coupled plasma mass spectrometry(fs-LA-MC-ICP-MS) for Zr isotopic analysis in zircons. The mass fractionation caused by instrumental mass discrimination was corrected by a combination of internal correction using Sr as an internal standard(coming from a NIST SRM 987 standard solution) and external correction using a matrix-matched standard. Several important instrument parameters were investigated, such as the effect of the addition of N;and "wet" plasma condition, the mass fractionation behaviors between Zr isotopes and Sr isotopes, the position effect in laser ablation cell and the effect of laser ablation parameters(laser spot size and energy density). The Zr isotope compositions of seven zircons(GJ-1, 91500, Ple?ovice, Rak-17, Paki, Aus and Mala) were determined by the developed fs-LAMC-ICP-MS and thermal ionization mass spectrometry(TIMS). Our fs-LA-MC-ICP-MS results for Zr isotope compositions agreed with TIMS analyses within analytical uncertainties, indicating the presented method is a suitable tool to resolve isotopic zoning in natural zircons. The results also suggest that GJ-1, 91500, Ple?ovice, Paki, Aus and Mala had the homogenous Zr isotope composition and could be considered as the potential candidates for the Zr isotope analysis in zircons, except Rak-17 which presented the large Zr isotope variation.

A new analytical mode and application of the laser ablation inductively coupled plasma mass spectrometer in the earth sciences

We proposed a new laser analytical mode,which used the high-frequency laser ablation to deliberately obtain the peak-shape signal profile,combined with the linear regression calibration(LRC)method to calculate elemental or isotopic ratios.In order to assess the performance of the new laser analytical mode for the application in the field of earth science,we systematically investigated the elemental quantitative analysis with high spatial resolution(10μm),rapid U-Pb dating in zircons and accurate Sr-Hf isotope analysis in geological samples.The new high-frequency laser analysis technology(20 Hz,100 pulses)reduced the limit of detection(LOD)of 25 elements to 0.005-0.16μg g^(-1) with crater diameters of 10μm,which are significantly lower(decrease to 2-20%)than previous researches.The quantitative analysis of five silicate glass reference materials showed that the precision and accuracy of the 25 trace elements(with the concentration ranging from 0.17 to 683μg g^(-1))were better than 16% and 15%,respectively.The new methods raised the analytical throughput of zircon U-Pb dating,Sr isotope ratios and Hf isotope ratios to 250 analyses per hour,144 analyses per hour and 120 analyses per hour in theory,while the analytical accuracy and precision were not affected.The detailed investigations showed that the proposed new laser analytical mode has good application effects in the field of earth sciences.