包气带介质截留不同龄垃圾渗滤液中的有机污染物

从渗滤液场龄和包气带岩性两方面着手,研究了不同岩性包气带介质对不同场龄渗滤液中有机污染物的截留作用规律。结果表明:新渗滤液经过以细砂、亚粘土为介质的包气带后,细砂和亚粘土中有机物的质量分数分别从0.70%和0.87%增大至0.80%和1.00%以上,而老渗滤液使细砂和亚粘土中有机物的质量分数降至0.70%和0.50%以下。新渗滤液经过包气带后,包气带介质中有机物的含量增大,而老渗滤液使包气带介质中有机物的含量降低,亚粘土较细砂更容易受到渗滤液污染的影响。即渗滤液性质对包气带介质中有机物含量具有方向性的影响作用,而包气带介质亚粘土比细砂更容易放大这种作用效果。     

中国中新生代咸化湖盆烃源岩沉积的问题及相关进展

我国东部断陷湖盆和西部坳陷湖盆第三系均有蒸发岩与烃源岩共生现象。前者水体深、咸化范围小，在氯化盐和碳酸盐沉积环境中形成了优质烃源岩，后者水体浅、咸化范围大，在氯化盐和硫酸盐沉积环境中发育了优质烃源岩，作者认为两种湖盆出现的水体分层是有机质堆积和保存的重要条件。济阳坳陷和柴达木盆地为两类咸化湖盆的典型代表，对它们的研究可以深化蒸发岩-烃源岩共生区油气地质的认识、促进勘探发展。     

Barium Isotopic Compositions in Thirty‐Four Geological Reference Materials Analysed by MC‐ICP‐MS

Measurement of Ba isotope ratios of widely available reference materials is required for interlaboratory comparison of data. Here, we present new Ba isotope data for thirty‐four geological reference materials, including silicates, carbonates, river/marine sediments and soils. These reference materials (RMs) cover a wide range of compositions, with Ba mass fractions ranging from 6.4 to 1900 µg g^?1, SiO₂ from 0.62% to 90.36% m/m and MgO from 0.08% to 41.03% m/m. Accuracy and precision of our data were assessed by the analyses of duplicate samples and USGS rock RMs. Barium isotopic compositions for all RMs were in agreement with each other within uncertainty. The variation of δ^138/134Ba in these RMs was up to 0.7‰. The shale reference sample, affected by a high degree of chemical weathering, had the highest δ^138/134Ba (0.37 ± 0.03‰), while the stream sediment obtained from a tributary draining carbonate rocks was characterised by the lowest δ^138/134Ba (?0.30 ± 0.05‰). Geochemical RMs play a fundamental role in the high‐precision and accurate determination of Ba isotopic compositions for natural samples with similar matrices. Analyses of these RMs could provide universal comparability for Ba isotope data and enable assessment of accuracy for interlaboratory data.     

川滇黔二叠系铅锌成矿物质来源：C-H-O-S-Pb同位素制约——以云南太平子铅锌矿为例

【研究目的】川滇黔地区铅锌矿成因具有多样性,特别是与峨眉山玄武岩的关系存在较大的争议,本文从前人关注较少的二叠系碳酸盐岩中的铅锌矿入手,研究成矿物质来源。【研究方法】以云南寻甸县太平子铅锌矿为研究对象,运用S、Pb、C、H、O同位素实验数据及流体包裹体测温等方法,对成矿物质来源及成矿流体特征进行探讨。【研究结果】矿石铅同位素组成比较均一,分布集中,²⁰⁶Pb/²⁰⁴Pb、²⁰⁷Pb/²⁰⁴Pb、²⁰⁸Pb/²⁰⁴Pb的变化范围分别为18.543～18.584、15.646～15.694、38.799～38.958,属于正常普通铅,具壳源特征,主要来源于基底岩石,水岩反应可能使赋矿围岩贡献少量的成矿物质。矿石硫化物δ³⁴S变化范围为-13.6‰～-7.3‰,方铅矿的δ³⁴S高于闪锌矿,硫同位素分馏并未达到平衡,生物成因硫酸盐还原作用（BSR）是还原硫的主要来源。热液方解石δ¹³C_V-PDB范围为3.8‰～4.7‰,δ¹⁸O_V-SMOW范围为12.0‰～16.7‰,相较于滇东北其他重要的铅锌矿床,具有明显的低δD、高δ¹⁸O_fluid特点,成矿流体中的水主要来源于岩浆水和有机水的混合,具有中—高温、低盐度特征。【结论】太平子铅锌矿在成矿物质、流体、成矿温度等均与区域上其他典型铅锌矿有较明显差别,具有典型的岩浆-热液成因特点。     

湘中锡矿山锑矿床成矿物质来源的同位素示踪

本文利用放射成因同位素（Pb、Sr)和轻稳定同位素（C、O）对锡矿山超大型锑矿床的成矿物质来源进行了示踪，从物源角度揭示了其在规模成矿、元素发生超常富集的原因。研究表明，锡矿山锑矿床的成矿物质不可能是来自赋矿围岩；深部地幔和基底都卷入了该矿的成矿作用；富Sb的交代型地幔和富Sb的元古界基底为其大规模成矿提供了充足的矿源，两者是形成锡成山超大型锑矿床的前提条件。     

The δ60/58Ni Values of Twenty‐Six Selected Geological Reference Materials

The high‐precision δ^60/58Ni values of twenty‐six geological reference materials, including igneous rocks, sedimentary rocks, stream sediments, soils and plants are reported. The δ^60/58Ni values of all samples were determined by double‐spike MC‐ICP‐MS (Nu Plasma III). Isotope standard solution (NIST SRM 986) and geological reference materials (BHVO‐2, BCR‐2, JP‐1, PCC‐1, etc.) were used to evaluate the measurement bias and intermediate precision over a period of six months. Our results show that the intermediate precision of Ni isotope determination was 0.05‰ (2s, n = 69) for spiked NIST SRM 986 and typically 0.06‰ for actual samples, and the δ^60/58Ni _{NIST SRM 986} values were in excellent agreement with previous studies. Eighteen high‐precision Ni isotope ratios of geological reference materials are first reported here, and their δ^60/58Ni values varied from ?0.27‰ to 0.52‰, with a mean of 0.13 ± 0.34‰ (2s, n = 18). Additionally, SGR‐1b (0.56 ± 0.04‰, 2s), GSS‐1 (?0.27 ± 0.06‰, 2s), GSS‐7 (?0.11 ± 0.01‰, 2s), GSD‐10 (0.46 ± 0.06‰, 2s) and GSB‐12 (0.52 ± 0.06‰, 2s) could potentially serve as candidate reference materials for Ni isotope fractionation and comparison of Ni isotopic compositions among different laboratories.     

Discriminating characters of ore-forming intrusions in the super-large Chalukou porphyry Mo deposit,NE China

The Chalukou porphyry Mo deposit, located in the Great Hinggan Range, is the largest Mo deposit in northeast China, although the age and genesis of the associated magmatic intrusions remain debated.Here we report zircon U-Pb ages and trace elements, whole rock geochemistry and Sre Nd isotope data with a view to understand the relationship between the magmatism and molybdenum mineralization.Zircon U-Pb analysis yield an age of 475 Ma for rhyolite in the older strata, 168 Ma for the premineralization monzogranite, and 154 Ma for the syn-mineralization granite porphyry. The granite porphyry and quartz porphyry are considered as the ore-forming intrusions. These rocks are peraluminous, alkali-calcic, and belong to high-K to shoshonitic series with a strong depletion of Eu. They also display characteristics of I-type granites. The rocks exhibit wide variations of(87 Sr/86 Sr)iin the range of 0.705426 -0.707363, and ε_(Nd)(t) of -3.7 to 0.93. Zircon REE distribution patterns show characteristics between crust and the mantle, implying magma genesis through crust-mantle interaction. The Fe_2O_3/FeO values(average 1) for the whole rock and EuN/Eu*Nvalues(average 0.45), Ce~(4+)/Ce~(3+) values(average 301)for zircon grains from the granite porphyry are higher than those from other lithologies. These features suggest that the ore-forming intrusions(syn-mineralization porphyry) had higher oxygen fugacity conditions than those of the pre-mineralization and post-mineralization rocks. The Chalukou Mo deposit formed in relation to the southward subduction of the Mongol-Okhotsk Ocean. Our study suggests that the subduction-related setting, crust-mantle interaction, and the large-scale magmatic intrusion were favorable factors to generate the super-large Mo deposits in this area.     

High‐Precision Measurement of 187Os/188Os Isotope Ratios of Nanogram to Picogram Amounts of Os in Geological Samples by N‐TIMS using Faraday Cups Equipped with 1013 Ω Amplifiers

N(¹⁸⁷Os)/N(¹⁸⁸Os) ratios of six geological reference materials were measured using static Faraday cups (FCs) with 10¹³ Ω amplifiers by N‐TIMS. Our results show that the repeatability precision was 2–3‰ (2 RSD, n = 3), when taking ~ 1 g of BHVO‐2 with 76 pg g^?1 of Os mass fraction and ~ 2 g of BCR‐2 with 21 pg g^?1 of Os mass fraction for each sample, whether measured by FCs or by secondary electron multiplier. The repeatability precision measured by FCs was 1–0.2‰ (2 RSD, n = 3) when taking ~ 1 g of BIR‐2 with 350 pg g^?1 of Os mass fraction, ~ 1 g of WGB‐1 with 493 pg g^?1 of Os mass fraction or ~ 0.5 g of WPR‐1 with 13.3 ng g^?1 of Os mass fraction for each sample, which is much better than those measured by secondary electron multiplier. Instead, when taking ~ 2 g of AGV‐2 with 4 pg g^?1 Os mass fraction, the repeatability precision measured by secondary electron multiplier is 3–4‰ (RSD, n = 3), which is better than those measured by FCs. Of the six reference materials analysed, WPR‐1 and BIR‐1a are the most homogeneous with regard to Os isotopic composition (2 RSD of 0.08% and 0.23%, respectively) when test portion masses are 0.5–1 g.     

Iron(II) oxide determination in rocks and minerals

The determination of FeO of geologic materials by modern instrumental methods (such as atomic absorption spectroscopy (AAS), inductively coupled plasma atomic emission spectroscopy (ICP-AES), X-ray fluorescence (XRF), etc.) cannot distinguish between different oxidation states of elements. In many cases, the oxidation state of Fe has to be known in order to perform several chemical calculations (norms, etc.) and discuss the reactions that occur during weathering, hydrothermal alteration and other processes. A modified Wilson method is proposed, giving reproducible results in a much shorter time than the classical method. Back-titration with potassium dichromate and an Fe(II) and ammonia sulphate solution is used, after dissolution of the sample powder in a heated HF/H₃PO₄ mixture and an ammonium vanadate solution. This modified method, tested with several international reference materials, gives reliable results, equivalent to the ones cited in the literature for the reference materials.     

新疆库木库里盆地演化

通过对新疆库木库里盆地的地质调查，渐新统一上新统识别出冲积扇、河流、湖泊三角洲、湖泊四种沉积相、六种亚相、十种微相；具有盆地演化早、晚期碎屑成熟度较低，盆地演化中期碎屑成熟度较高的特征；通过物源分析得出盆地演化早期碎屑物质来自盆地南部，晚期碎屑物质来自盆地西部，碎屑物质均来源于再旋回造山带构造背景区，并具有早期南高北低、晚期西南高东北低的古地理格局；盆地分析表明新疆库木库里盆地从渐新世形成大致经历了渐新世一早中新世盆地萌芽、中中新世一晚中新世盆地的生长发育、上新世盆地萎缩三个演化阶段。