The geochemistry of gem opals as evidence of their origin     

Eloïse Gaillou  Aurlien Delaunay  Benjamin Rondeau  Martine Bouhnik-le-Coz  Emmanuel Fritsch  Guy Cornen  Christophe Monnier 《Ore Geology Reviews》2008,34(1-2):113

Seventy-seven gem opals from ten countries were analyzed by inductively coupled plasma-mass spectrometry (ICP-MS) through a dilution process, in order to establish the nature of the impurities. The results are correlated to the mode of formation and physical properties and are instrumental in establishing the geographical origin of a gem opal. The geochemistry of an opal is shown to be dependant mostly on the host rock, at least for examples from Mexico and Brazil, even if modified by weathering processes. In order of decreasing concentration, the main impurities present are Al, Ca, Fe, K, Na, and Mg (more than 500 ppm). Other noticeable elements in lesser amounts are Ba, followed by Zr, Sr, Rb, U, and Pb. For the first time, geochemistry helps to discriminate some varieties of opals. The Ba content, as well as the chondrite-normalized REE pattern, are the keys to separating sedimentary opals (Ba > 110 ppm, Eu and Ce anomalies) from volcanic opals (Ba < 110 ppm, no Eu or Ce anomaly). The Ca content, and to a lesser extent that of Mg, Al, K and Nb, helps to distinguish gem opals from different volcanic environments. The limited range of concentrations for all elements in precious (play-of-color) compared to common opals, indicates that this variety must have very specific, or more restricted, conditions of formation. We tentatively interpreted the presence of impurities in terms of crystallochemistry, even if opal is a poorly crystallized or amorphous material. The main replacement is the substitution of Si⁴⁺ by Al³⁺ and Fe³⁺. The induced charge imbalance is compensated chiefly by Ca²⁺, Mg²⁺, Mn²⁺, Ba²⁺, K⁺, and Na⁺. In terms of origin of color, greater concentrations of iron induce darker colors (from yellow to “chocolate brown”). This element inhibits luminescence for concentrations above 1000 ppm, whereas already a low content in U (≤ 1 ppm) induces a green luminescence.  相似文献   

冀北—辽西早白垩世沉积有机质特征与古气候环境演变     

李洪涛  宋之光  邹艳荣  王成善  季强 《地质学报》2008,82(1):72-76

本文对冀北—辽西地区早白垩世沉积盆地富有机质沉积岩进行了初步有机地球化学分析研究。结果显示,冀北—辽西沉积盆沉积有机质特征在时间和空间上存在很大差异,代表白垩系早期沉积的滦平盆地大北沟组有机质丰度低,这不仅显示其所代表的沉积相带不利于有机质的聚集,也反映了当时生物不够繁盛;大店子组时期沉积相带发生了变化,有机质类型随着发生了变化,丰度有所增高,但总体上显示环境条件不利于生物的发育和繁盛。到了桥头组和义县组沉积岩有机质丰度大幅升高,表明生物界非常繁盛,古气候环境有利于有机质的大量生成和堆积,总体上反映了温湿的气候条件;但同时也存在较为频繁或交替性寒冷气候波动,具体的古气候环境状态尚需进一步深入研究。  相似文献   

藏南白垩系黑-红层沉积岩有机质组成分布特征   总被引：1，自引：0，他引：1  

傅培刚  宋之光  胡修棉  王成善 《地质学报》2008,82(1):85-91

对藏南江孜县床得剖面白垩系黑层和红层沉积岩进行的有机地球化学研究表明,黑层有机碳含量高于红层5～10倍,红层和黑层饱和烃主峰碳数分别为nC25和nC23;黑层和红层沉积有机质的母质来源都以水生植物和菌藻类等低等生物为主,陆源有机质的输入非常有限;但饱和烃的分布和主峰碳数的差异可能反映了有机母源物质在种群方面的差异,而这种差异可能主要是水体温度存在差异造成的,即红层发育时期水体温度可能高于黑层沉积时期.而在高温度条件下,水生生物和陆生植物的生长发育受到限制,造成原始有机质产率和有机质沉积保存量低可能是红层沉积岩形成的主要原因.  相似文献   

Sulfur isotope measurement of sulfate and sulfide by high-resolution MC-ICP-MS   总被引：4，自引：0，他引：4  

Paul R. Craddock  Olivier J. Rouxel  Lary A. Ball  Wolfgang Bach   《Chemical Geology》2008,253(3-4):102-113

We have developed a technique for the accurate and precise determination of ³⁴S/³²S isotope ratios (δ³⁴S) in sulfur-bearing minerals using solution and laser ablation multiple-collector inductively coupled plasma mass spectrometry (MC-ICP-MS). We have examined and determined rigorous corrections for analytical difficulties such as instrumental mass bias, unresolved isobaric interferences, blanks, and laser ablation- and matrix-induced isotopic fractionation. Use of high resolution sector-field mass spectrometry removes major isobaric interferences from O₂⁺. Standard-sample bracketing is used to correct for the instrumental mass bias of unknown samples. Background on sulfur masses arising from memory effects and residual oxygen-tailing are typically minor (< 0.2‰, within analytical error), and are mathematically removed by on-peak zero subtraction and by bracketing of samples with standards determined at the same signal intensity (within 20%). Matrix effects are significant (up to 0.7‰) for matrix compositions relevant to many natural sulfur-bearing minerals. For solution analysis, sulfur isotope compositions are best determined using purified (matrix-clean) sulfur standards and sample solutions using the chemical purification protocol we present. For in situ analysis, where the complex matrix cannot be removed prior to analysis, appropriately matrix-matching standards and samples removes matrix artifacts and yields sulfur isotope ratios consistent with conventional techniques using matrix-clean analytes. Our method enables solid samples to be calibrated against aqueous standards; a consideration that is important when certified, isotopically-homogeneous and appropriately matrix-matched solid standards do not exist. Further, bulk and in situ analyses can be performed interchangeably in a single analytical session because the instrumental setup is identical for both. We validated the robustness of our analytical method through multiple isotope analyses of a range of reference materials and have compared these with isotope ratios determined using independent techniques. Long-term reproducibility of S isotope compositions is typically 0.20‰ and 0.45‰ (2σ) for solution and laser analysis, respectively. Our method affords the opportunity to make accurate and relatively precise S isotope measurement for a wide range of sulfur-bearing materials, and is particularly appropriate for geologic samples with complex matrix and for which high-resolution in situ analysis is critical.  相似文献   

The relationship between hydrodynamic properties and weathering of soils derived from volcanic rocks,Galapagos Islands (Ecuador)     

M. Adelinet  J. Fortin  N. d’Ozouville  S. Violette 《Environmental Geology》2008,56(1):45-58

The aim of this interdisciplinary study is to examine a component of the hydrological cycle in Galapagos by characterizing soil properties. Nine soil profiles were sampled on two islands. Their physical and hydrodynamic properties were analyzed, along with their mineralogical composition. Two groups of soils were identified, with major differences between them. The first group consists of soils located in the highlands (>350 m a.s.l.), characterized by low hydraulic conductivity (<10⁻⁵ m s⁻¹) and low porosity (<25%). These soils are thick (several meters) and homogeneous without coarse components. Their clay fraction is considerable and dominated by gibbsite. The second group includes soils located in the low parts of the islands (<300 m a.s.l.). These soils are characterized by high hydraulic conductivity (>10⁻³ m s⁻¹) and high porosity (>35%). The structure of these soils is heterogeneous and includes coarse materials. The physical properties of the soils are in good agreement with the variations of the rainfall according to the elevation, which appears as the main factor controlling the soil development. The clayey alteration products constrain soils physical and hydrodynamic properties by reducing the porosity and consequently the permeability and also by increasing water retention.  相似文献   

Mapping susceptibility of rainfall-triggered shallow landslides using a probabilistic approach   总被引：2，自引：0，他引：2  

Chia-Nan Liu  Chia-Chen Wu 《Environmental Geology》2008,55(4):907-915

To prepare a landslide susceptibility map is essential to identify hazardous regions, construct appropriate mitigation facilities, and plan emergency measures for a region prone to landslides triggered by rainfall. The conventional mapping methods require much information about past landslides records and contributing terrace and rainfall. They also rely heavily on the quantity and quality of accessible information and subjectively of the map builder. This paper contributes to a systematic and quantitative assessment of mapping landslide hazards over a region. Geographical Information System is implemented to retrieve relevant parameters from data layers, including the spatial distribution of transient fluid pressures, which is estimated using the TRIGRS program. The factor of safety of each pixel in the study region is calculated analytically. Monte Carlo simulation of random variables is conducted to process the estimation of fluid pressure and factor of safety for multiple times. The failure probability of each pixel is thus estimated. These procedures of mapping landslide potential are demonstrated in a case history. The analysis results reveal a positive correlation between landslide probability and accumulated rainfall. This approach gives simulation results compared to field records. The location and size of actual landslide are well predicted. An explanation for some of the inconsistencies is also provided to emphasize the importance of site information on the accuracy of mapping results.  相似文献   

In situ strength measurements on natural upper-mantle minerals   总被引：1，自引：0，他引：1  

Junji Yamamoto  Jun-ichi Ando  Hiroyuki Kagi  Toru Inoue  Akihiro Yamada  Daisuke Yamazaki  Tetsuo Irifune 《Physics and Chemistry of Minerals》2008,35(5):249-257

Using in situ strength measurements at pressures up to 10 GPa and at room temperature, 400, 600, and 700°C, we examined rheological properties of olivine, orthopyroxene, and chromian-spinel contained in a mantle-derived xenolith. Mineral strengths were estimated using widths of X-ray diffraction peaks as a function of pressure, temperature, and time. Differential stresses of all minerals increase with increasing pressure, but they decrease with increasing temperature because of elastic strain on compression and stress relaxation during heating. During compression at room temperature, all minerals deform plastically at differential stress of 4–6 GPa. During subsequent heating, thermally induced yielding is observed in olivine at 600°C. Neither orthopyroxene nor spinel shows complete stress relaxation, but both retain some stress even at 700°C. The strength of the minerals decreases in the order of chromian-spinel ≈ orthopyroxene > olivine for these conditions. This order of strength is consistent with the residual pressure of fluid inclusions in mantle xenoliths.  相似文献   

黑龙江省金厂金矿床J0矿体流体地球化学研究   总被引：7，自引：6，他引：1  

张宇  赖勇  卿敏  王艳忠  徐佳佳 《岩石学报》2008,24(5)

黑龙江省东宁县金厂金矿床是最新发现的特大型金矿床,目前探获黄金资源量86吨,它位于中亚造山带东端的吉黑成矿带,是与中生代中酸性岩浆活动有关的复杂成矿系统,矿化类型可能包括了斑岩型、爆破角砾岩型、浅成低温热液型.研究表明,高丽沟J0号矿体为爆破角砾岩型,热液成矿过程经历了早、中、晚3个阶段,分别形成以石英-黄铁矿、多金属硫化物-石英和碳酸盐为代表的矿物组合,中阶段矿物含自然金最多,次为早阶段矿物.初始成矿流体系统为高温、高盐度、高氧逸度、富CO2的岩浆热液;经减压沸腾,CO2等挥发分大量逸出,流体温度、盐度和氧逸度下降,导致大量金属硫化物及自然金快速沉淀;大气降水混入导致晚阶段流体低温、低盐度、贫CO2,对成矿贡献甚微.总体而言,成矿流体盐度高(11.70%～37.81%NaCl.eq),成矿作用发生在中-高温(238.3～425.7℃)的浅成环境(深633m～2736m).岩浆-流体成矿系统富CO2应发育于大陆碰撞造山带的伸展构造背景,而非大洋板块俯冲诱发的岩浆弧背景.  相似文献   

河南省洛宁县寨凹钼矿床流体包裹体研究及矿床成因   总被引：10，自引：0，他引：10  

邓小华陈衍景  姚军明李文博李 诺王 运糜 梅张 颖 《中国地质》2008,35(6):1250-1266

寨凹钼矿床位于华北克拉通南缘的熊耳地体．矿床定位受马超营断裂带的次级断裂控制,矿体呈脉状贼存于太华超群石板沟组黑云角闪斜长片麻岩中。成矿过程包括3个阶段：石英-辉钼矿阶段（I）、石英-多金属硫化物阶段（Ⅱ）、石英-碳酸盐阶段（Ⅲ）,其中,I阶段为主成矿阶段。寨凹钼矿床可见2类流体包裹体,即水溶液型和含子晶包裹体;激光拉曼指示包裹体成分主要为H2O。从早到晚,流体包裹体均一温度从I阶段100～260℃,经Ⅱ阶段110～160℃．变化为Ⅲ阶段120—180℃．矿床总体属于低温热液矿床：流体包裹体盐度从I阶段的2～25wt％NaCl．eqv演化至Ⅱ阶段的6—30wt％NaCl．eqv．然后降为Ⅲ阶段的7～25wt％NaCl．eqv。I阶段均一温度范围宽广、流体包裹体盐度由双峰式演化为单峰式以及包裹体温度-盐度双变图的负相关性指示了流体混合是主要的成矿机制。寨凹钼矿流体包裹体以高密度、高盐度的低温低压流体为特征,是含CaCl,流体参与成矿的结果,热的岩浆流体与冷的含CaCl,的卤水的混合．导致了辉钼矿的沉淀。寨凹钼矿床地质和流体包裹体特征与侵入岩相关的成矿系统一致．指示其成因类型为与侵入岩有关的钼矿床．  相似文献   

安徽铜陵朝山金矿床流体包裹体研究   总被引：3，自引：1，他引：2  

杨小男  徐兆文  高庚  陆现彩  刘苏明  李海勇 《岩石学报》2008,24(8)

朝山金矿床是狮子山矿田内的热液交代型金矿床,在成因上与燕山期的白芒山辉石闪长岩有关.通过采集发育在不同深度下的含金黄铁矿-石英一方解石脉样品,进行流体包裹体岩相学观察和显微测温发现,石英和方解石中均捕获了富气相、富液相的两相水溶液包裹体和含子晶的三相水溶液包裹体,以上三种类型包裹体的均一温度统计峰值分别出现于315～335℃和255～275℃,盐度的统计峰值出现于17.50%～22.50%NaCl eq.和32.50%～37.50%NaCl eq.之间.激光拉曼探针分析表明,石英中流体包裹体的气相成分以水蒸汽为主,伴有少量CO2,可能含有CH4.流体的H、O同位素组成具确岩浆水特征.上述研究表明.朝山金矿成矿流体经历了相态变化,发生了不均匀捕获.受燕山期岩浆作用影响,狮子山矿田内的铜、金成矿在时空上具有一定联系,成矿流体运移的过程中,主要发生了相分离、气相液化和减压沸腾作用,可能是形威铜、金矿化分带的重要原因.  相似文献