论川西炉霍裂谷微细浸染型金矿的矿质来源

扼要介绍了川西炉霍裂谷微细浸染型金矿的地质特征, 通过地层和岩石中元素丰度特征,稀土元素、同位素、微量金的可化性实验等系统分析, 提出炉霍裂谷微细浸染型金矿的成矿物质来自三叠纪地层中的细碎屑质浊积岩建造和裂谷海底火山作用提供的深源物质。并讨论了矿质初始富集的机制。     

泌阳断陷下第三系核三上段高频层序中米兰柯维奇天文旋回信息

古气候是影响陆相层序发育的一个重要因素,其周期性变化是源于天文旋回的驱动力（即米兰柯维奇假说）。米兰柯维奇天文旋回包括偏心率旋回、倾斜率旋回和岁差旋回,这几个轨道参数所驱动的古气候变迁,分别形成了周期为１０万年（或４０万年）、４万年及２万年的高频层序,即小层序组、小层序及小层单元,研究结果表明,泌阳断陷湖盆的高频层序是由地球轨道旋回所驱动的古气候周期性变迁所形成的。     

GGR Biennial Critical Review: Analytical Developments Since 2014

This GGR biennial critical review covers developments and innovations in key analytical methods published since January 2014, relevant to the chemical, isotopic and crystallographic characterisation of geological and environmental materials. In nine selected analytical fields, publications considered to be of wide significance are summarised, background information is provided and their importance evaluated. In addition to instrumental technologies, this review also presents a summary of new developments in the preparation and characterisation of rock, microanalytical and isotopic reference materials, including a précis of recent changes and revisions to ISO guidelines for reference material characterisation and reporting. Selected reports are provided of isotope ratio determinations by both solution nebulisation MC‐ICP‐MS and laser ablation‐ICP‐MS, as well as of radioactive isotope geochronology by LA‐ICP‐MS. Most of the analytical techniques elaborated continue to provide new applications for geochemical analysis; however, it is noted that instrumental neutron activation analysis has become less popular in recent years, mostly due to the reduced availability of nuclear reactors to act as a neutron source. Many of the newer applications reported here provide analysis at increasingly finer resolution. Examples include atom probe tomography, a very sensitive method providing atomic scale information, nanoscale SIMS, for isotopic imaging of geological and biological samples, and micro‐XRF, which has a spatial resolution many orders of magnitude smaller than conventional XRF.     

构造活动地区工程构造稳定性研究

拟建的新疆喀拉喀什河乌鲁瓦提水电站位于现代地壳运动十分活跃的区域。野外证据显示出，坝区的Ｆ＿（１２）断层新活动延续到晚更新世，电站附近的石门北断层在第四纪有活动。对采自坝区及附近几条断层的断层物质样品进行了变形显微构造、石英颗粒表面形貌和微结构类型、ＴＬ年龄的分析测定，结果表明，Ｆ＿（１２）最新活动的上限时间不晚于３万年，Ｆ＿（３０）和石门断层的活动持续到晚更新世，石门北断层最新的活动的上限时间约２万年。根据区域断裂的分布和应力场的情况，进行了构造模拟实验，预测出工程区在区域应力场的继续作用下，应力集中在远离坝址的部位，坝址附近不会出现新的应力集中点。总体看，所选坝址是地壳活动区中相对较稳定的地段。     

胶西北新城金矿床硫同位素地球化学

新城金矿床是胶西北金矿集区中典型的破碎带蚀变岩型金矿床,其热液成矿作用可划分为四个阶段:黄铁矿-石英-绢云母阶段(I)、石英-黄铁矿阶段(II)、石英-多金属硫化物阶段(III)和石英-方解石阶段(IV),其中金主要赋存于II和III阶段的黄铁矿内。该矿床赋矿围岩为郭家岭岩体,岩性为石英二长岩和二长花岗岩,主要为胶东群变质基底经部分熔融形成。胶东群变粒岩硫同位素较为均一(δ34S值介于6.9‰~9.4‰,均值为8.0‰);郭家岭岩体的δ34S值介于6.0‰~16.0‰,均值为8.6‰,反映了其硫同位素组成总体上继承了变粒岩的硫同位素特征;长英质脉岩的δ34S值变化范围为0.8‰~8.5‰(均值为6.7‰),其中4件样品的δ34S值变化范围为7.4‰~8.5‰,反映了其硫主要源自于郭家岭岩体,变粒岩可能提供了部分硫源;而其中1件样品的δ34S值仅为0.8‰,符合岩浆硫来源特征,表明深部岩浆可能也提供了部分硫源。新城金矿床矿石中硫化物δ34S值变化范围较大(4.3‰~10.6‰,均值为8.3‰),表明矿石硫可能源于郭家岭岩体、变粒岩和长英质脉岩,最终主要来源于胶东群变质基底。I阶段黄铁矿颗粒较小(5~600μm),晶形主要为立方体,反映其处于温度较高(300~350℃)、成矿流体的过饱和度较低、低氧逸度和硫逸度、冷却快速、物质供应不足的成矿环境;黄铁矿δ34S值变化范围为8.4‰~10.6‰,均值为9.7‰,反映了矿石硫可能源自于δ34S值较高的郭家岭岩体和变粒岩。II和III阶段黄铁矿粒径变化较大(3μm~2.5mm),晶形主要为五角十二面体,反映其处于中-低温度(200~300℃)、成矿流体过饱和度高、高氧逸度和硫逸度、缓慢冷却同时物质供应充分的成矿环境。其中,II阶段黄铁矿δ34S值变化范围为7.7‰~9.7‰,均值为8.7‰,表明矿石硫源除郭家岭岩体和变粒岩外,δ34S值较低的长英质脉岩可能也提供了部分硫源。III阶段硫化物δ34S值变化范围较大(4.3‰~9.4‰,均值为7.1‰),闪锌矿-方铅矿硫同位素热力学平衡温度范围为180~282℃,氧逸度约为10-37.3~10-36.8,反映了矿石硫源自于郭家岭岩体、变粒岩和长英质脉岩,硫化物δ34S值变化范围较大可能是硫同位素分馏达到平衡的结果。IV阶段黄铁矿粒径最小(1~5μm),为晶形完好、表面光滑的立方体晶形,表明其处于较低温度(200℃),成矿流体的过饱和度较低、氧逸度和硫逸度较低、物质供应不足的成矿环境。     

中国近海沉积物氮和有机碳标准物质的研制

我国海洋沉积物的研究近几年发展较快,但是缺少有定值的氮、有机碳标准物质。本文针对及其匮乏的氮、有机碳国家二级标准物质进行了我国近海沉积物总氮(TN)、总碳(TC)、总有机碳(TOC)含量的分析标准参考物质的研制。研究样品采自"我国近海海洋综合调查与评价"专项提供的表层沉积物,经过冷冻干燥、研磨至74μm,使用元素分析仪和氧化热解-气相色谱法分析总氮和总碳的含量;使用元素分析仪和氧化热解-电位法分析总有机碳的含量,制备了一系列16个有定值的总氮、总碳、总有机碳含量的近海沉积物标准物质。样品在均匀性检验中,F的实测值小于临界值,相对偏差较小,样品的均匀性较好。在稳定性检验方面,两年内多次测定的分析结果无方向性变化,统计计算结果显示稳定性良好。本文研制的这16个近海沉积物标准物质在3家实验室进行了联合定值,按照ISO导则35和国家一级标准物质研制规范,给出了该系列标准物质总氮、总碳、总有机碳含量的标准值和不确定度。这批标准物质分为不同海区,不同海区的标准物质又分为不同的沉积物类型,研制的不同海区不同沉积物类型的标准物质对现有的海洋沉积物标准物质进行了有效的补充。     

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。     

藏南拉木由塔锑(金)矿床S、Pb同位素组成及指示意义

西藏拉木由塔锑(金)矿床位于藏南Sb - Au成矿带东段,矿(化)体主要赋存于中侏罗统遮拉组地层与辉绿(玢)岩脉接触带上.在分析该矿床成矿地质条件的基础上,系统研究了矿石硫、铅同位素组成特征,并通过与区域成矿带中典型矿床硫、铅同位素组成的对比分析,探讨了矿床成矿物质来源.研究表明矿石硫化物的硫同位素组成变化范围较窄,成...