柴达木盆地侏罗纪古气候演变过程：来自化学风化特征的证据

柴达木盆地侏罗系陆相地层记录了该时期一系列重大的构造—气候—环境耦合演化事件，然而针对该套地层的古气 候、古风化作用等方面研究还很薄弱。为了恢复柴达木盆地侏罗纪时期的古气候和古环境特征，文章研究对柴北缘大煤沟侏 罗系标准剖面的沉积岩样品开展了全岩主、微量元素测试，综合采用多种化学风化指数判定柴达木盆地侏罗纪古气候条件及 演变过程。元素比值(Rb/Sr、K/Na、Na/Al 和Na/Ti)和化学风化指数(CIA、CIW、PIA 和ICV)均显示，柴达木盆地侏罗纪化学风 化过程和古气候演化过程可划分为4 个阶段：早侏罗世早—中期和中侏罗世中期，化学风化作用强烈，古气候处于温带—亚热 带温暖、潮湿气候条件；早侏罗世晚期和中侏罗世晚期—晚侏罗世，受到区域降水减少影响，盆地化学风化作用显著减弱，整体 处于干旱、半干旱环境。以上结果与前人基于沉积物和植物群面貌研究得出的古气候变化过程相吻合，为盆地及区域陆相侏 罗纪古气候研究提供了相对完整而连续的地球化学证据和参考。     

临安一次沙尘暴过程影响气溶胶物理化学特性演变的初步分析

文章利用2002年3月29日～4月4日在浙江临安大气本底污染监测站观测的气溶胶粒子质量谱、离子与元素成分的数据,结合TOMS卫星的气溶胶指数资料和轨迹模式,重点分析在北方沙尘暴输送影响期间临安气溶胶质量浓度尺度分布的演变特点以及气溶胶化学成分与不同空气来源的关系。初步分析结果显示,受北方沙尘暴天气影响,临安气溶胶质量浓度、离子、元素浓度有明显的尺度分布演变。这种演变与污染物来源和大气污染物的气粒转化有关。沙尘影响前和结束后临安地区气溶胶主要以细粒子为主(<2.1μm),峰值粒径0.65～2.1μm,而受北方地区的沙尘暴影响,峰值粒径偏移到2.1～3.3μm,且在7～11μm间出现另一个峰值,同时临安气溶胶粗粒子中矿物元素显著增加。从离子成分看,在整个观测期间SO^2-₄与NH⁺₄在细粒子段有很好的一致性,而SO^2-₄,NO^-₃与Ca²⁺在粗粒子段有很好的相关,尤其是沙尘影响期间NO^-₃与Ca²⁺有很好的对应关系,表现出较明显的表面非均相反应特征     

新西兰碧玉的宝石学特征

以产自新西兰的碧玉样品作为研究对象,采用常规的宝石学测试、傅里叶变换红外光谱仪、环境扫描电子显微镜、等离子体质谱仪、X射线粉晶衍射仪,对其表面微观形貌、矿物组成、化学成分特征进行了较全面的研究。研究表明,新西兰碧玉的显微结构致密程度不高,矿物结晶颗粒粗细不一,局部具有定向性,其主要的矿物组成为角闪石,内含黑色的铬铁矿杂质。将新西兰碧玉的化学成分特征与新疆一带所产的碧玉相比较,主量元素和微量元素的含量均有所差别。     

Determination of Precise and Accurate 51V/50V Isotope Ratios by MC‐ICP‐MS,Part 1: Chemical Separation of Vanadium and Mass Spectrometric Protocols

We present the first technique to obtain precise and accurate vanadium (V) stable isotope compositions by chemical isolation and multi‐collector inductively coupled plasma‐mass spectrometry (MC‐ICP‐MS). Separation of V from matrix elements was achieved via five separate ion exchange columns. The procedure quantitatively removed Ti and Cr, which contain direct isobaric interferences on the minor isotope ⁵⁰V. Isotope compositions were determined using a conventional standard solution‐sample bracketing technique. The V isotope composition for an in‐house secondary standard solution from BDH Chemicals was δ⁵¹V = ?1.19 ± 0.12‰ (2s, n = 600), measured as the per mil deviation relative to the composition of a widely available Specpure Alfa Aesar (AA) vanadium solution. This represents an improvement in measurement precision on previous techniques of almost two orders of magnitude. The effects of adding Cr, Ti and S to standard solutions were explored to determine the robustness of protocols. Only very low levels of these elements could be tolerated to obtain precise and accurate isotope compositions and was achieved with the chemical purification procedure. Standard solutions from AA and BDH processed as unknowns through the entire chemical separation and measurement protocols returned 100% yields and the same isotopic compositions as those of unprocessed standard solutions.     

丰予井田地下水化学特征分析及意义

了解地下水化学特征及其形成作用对于快速识别矿井突水水源、防止矿井突水具有重要意义。在系统分析丰予井田水文地质条件的基础上,运用各常规离子与TDS（溶解性固体总量）的二次拟合曲线、Piper三线图、离子浓度变异系数、地下水Stiff图、TDS等值线图、Gibbs图以及离子比例系数图对各含水层的地下水水化学特征及形成作用进行分析。研究结果表明：各含水层的离子浓度变异系数均小于1,离子的分布比较稳定;山西组和太原组的水化学类型均为HCO₃·Cl-Na+K·Ca,且Na⁺+K⁺与TDS浓度均较大,山西组和太原组是相对封闭的含水层,新生界和奥陶系的水化学类型为HCO₃-Ca·Mg;水岩作用是影响各含水层化学成分的主要作用,碳酸盐岩溶解、硅铝酸盐溶解以及蒸发岩溶解是影响地下水化学成分的主要因素。     

Metals and models: Diagenic modelling in freshwater lacustrine sediments

This review aims to distill and synthesize the existing information on the use of models to describe and predict the distribution and movement of metals in lacustrine sediments. As such it examines the causes of metal diagenesis, the origin and form of the equations that govern these phenomena, and the predictability or measurability of the parameters that appear in the models. The paper concludes by highlighting some seminal results from modelling studies, including the determination of the factors controlling the formation of surficial Mn-Fe-enriched zone or layers, the substantial contribution possible from metal reduction to organic matter regeneration, the calculation of mixing-corrected metal input histories to lakes, and the prediction of growth rates and morphologies for both deep-sea and lacustrine ferromanganese nodules.     

徐州睢宁白露山岩体中的铬铁矿化学成分及金刚石的含矿性研究

白露山岩体是苏北地区重要的金刚石含矿岩体。通过研究该岩体中的铬铁矿化学成分,探讨其成因及金刚石的含矿性,进一步分析金刚石的成矿潜力。白露山岩体中的铬铁矿具有高Cr、低Al、高Mg的特征,属于镁铬铁矿,是深部地幔橄榄岩结晶而成的,不是岩体本身的结晶产物,可能来源于岩体中的深源捕虏体。铬铁矿的结晶温度为1 253~1 354 ℃,与金刚石的形成温度(1 150~1 400 ℃)相近,二者关系密切。铬铁矿化学成分与山东、辽宁含矿金伯利岩中铬铁矿的化学成分较相似,多数属于S4组和S6组铬铁矿,少数属于S1组和S2组铬铁矿,其中S1组和S2组铬铁矿是含矿岩体的标型矿物。白露山岩体具有良好的金刚石成矿潜力和找矿前景。     

安徽沙溪斑岩铜（金）矿区闪长斑岩形成机制

沙溪铜（金）矿床是目前长江中下游成矿带中已探明储量最大的斑岩型铜矿床。文章通过对沙溪矿区内闪长斑岩的年代学、全岩化学成分、同位素地球化学等综合研究,探讨了闪长斑岩的形成机制。闪长斑岩的LA-ICP-MS锆石U-Pb加权平均年龄为128.3±1.5 Ma,属于早白垩世岩浆活动产物。岩石具有富碱（ALK=6.12~7.53 wt%）、富钾、富镁（Mg#=38.99~51.53）、准铝质（A/CNK=0.90~0.99）等特征,属于钙碱性—高钾钙碱性系列岩石;岩石轻稀土元素富集,重稀土元素亏损（LaN/YbN=12.63~17.63）,无明显的Eu异常（δEu=0.84~1.14）;大离子亲石元素（Ba、Sr）和Pb等富集,高场强元素（Nb、Ta、Ti等）亏损。闪长斑岩的全岩(87Sr/86Sr)t值为0.7052~0.7056,εNd(t )值为-6.09~-3.42,(206Pb/204Pb)t值为17.51~18.16、(207Pb/204Pb)t值为15.49~15.63、(208Pb/204Pb)t值为37.57~38.45,表明成岩物质源于壳幔混合。130 Ma左右,平移的郯庐断裂的伸展引发了大规模岩浆作用,来自深部的岩浆沿着郯庐断裂带上侵,并混染了大量的地壳物质,形成了沙溪闪长斑岩及与铜矿有关的石英闪长斑岩。     

CAMAM: A Miniature Laser Ablation Ionisation Mass Spectrometer and Microscope‐Camera System for In Situ Investigation of the Composition and Morphology of Extraterrestrial Materials

Performance studies of a microscope‐camera system (MCS) and a laser ablation/ionisation mass spectrometer (LIMS) instrument (referred to here as a laser mass spectrometer or LMS) are presented. These two instruments were designed independently for in situ analysis of solids on planetary surfaces and will be combined to a single miniature instrument suite for in situ chemical and morphological analysis of surface materials on planetary bodies. LMS can perform sensitive chemical (elemental, isotope and molecular) analyses with spatial resolution close to micrometre‐sized grains. It allows for studies with mass resolution (M/ΔM) up to 800 in ablation mode (elemental composition) and up to 1500 in desorption mode (molecular analysis). With an effective dynamic range of at least eight orders of magnitude, sensitive and quantitative measurements can be conducted of almost all elements and isotopes with a concentration larger than a few ppb atoms. Hence, in addition to the major element composition, which is important for the determination of mineralogical constituents of surface materials, trace elements can also be measured to provide information on mineral formation processes. Highly accurate isotope ratio measurements can be used to determine in situ geochronology of sample material and for investigations of various isotope fractionation processes. MCS can conduct optical imagery of mm‐sized objects at several wavelengths with micrometre spatial resolution for the characterisation of morphological surface details and to provide insight into surface mineralogy. Furthermore, MCS can help in the selection of sample surface areas for further mass spectrometric analysis of the chemical composition. Surface auto‐fluorescence measurements and images in polarised light are additional capabilities of the MCS, to identify either fluorescing minerals or organic materials, if present on the analysed surface, for further investigation by LMS. The results obtained by investigations of NIST reference materials, amino acid films and a natural graphite sample embedded in silicate rock are presented to illustrate the performance of the instruments and their potential to deliver chemical information for mineral and organic phases in their geological context.     

Intermediate granulite produced by transformation of eclogite at a felsic granulite contact,in Blanský les,Bohemian Massif

Layers or bodies of intermediate granulite on scales from a centimetre to a hundred metres occur commonly within the felsic granulite massifs of the Bohemian Massif. Their origin is enigmatic in that they commonly have complex microstructures that are difficult to interpret, and therefore even the sequence of crystallization of minerals is uncertain. At Kle?, in the Blanský les massif, there is a revealing outcrop in a low‐strain zone in which it is clear that intermediate granulite can form by the interaction of felsic granulite with eclogite. The eclogite, retains garnet from its eclogite heritage, the grains at least partially isolated from the matrix by a plagioclase corona. The original omphacite‐dominated matrix of the eclogite now consists of recrystallized diopsidic clinopyroxene, orthopyroxene and plagioclase, with minor brown amphibole and quartz. The modification of the eclogite is dominated by the addition of just K₂O and H₂O, rather than all the elements that would be involved if the process was one of pervasive melt infiltrations. This suggests that the main process involved is diffusion, with the source being the felsic granulite, or local partial melt of the granulite. The diffusion occurred at ~950 °C and 12 kbar, with the main observed effects being (i) the un‐isolation and preferential destruction of the interior part of some of the garnet grains by large idiomorphic ternary feldspar; (ii) textural modification of the matrix primarily involving the recrystallization of clinopyroxene into large poikiloblasts containing inclusions of ternary plagioclase; and (iii) conversion of low‐K plagioclase in the matrix into ternary feldspar by incorporation of the diffused‐in K₂O. The phase equilibria in the intermediate granulite are consistent with the chemical potential relationships that would be superimposed on the original eclogite by the felsic granulite at 950 °C and 12 kbar.