Ilmenite composition in the Tellnes Fe–Ti deposit,SW Norway: fractional crystallization,postcumulus evolution and ilmenite–zircon relation

Major and trace element XRF and in situ LA-ICP-MS analyses of ilmenite in the Tellnes ilmenite deposit, Rogaland Anorthosite Province, SW Norway, constrains a two stage fractional crystallization model of a ferrodioritic Fe-Ti-P rich melt. Stage 1 is characterized by ilmenite-plagioclase cumulates, partly stored in the lower part of the ore body (Lower Central Zone, LCZ), and stage 2 by ilmenite-plagioclase-orthopyroxene-olivine cumulates (Upper Central Zone, UCZ). The concentration of V and Cr in ilmenite, corrected for the trapped liquid effect, (1) defines the cotectic proportion of ilmenite to be 17.5 wt% during stage 1, and (2) implies an increase of D _V^Ilm during stage 2, most likely related to a shift in fO₂. The proportion of 17.5 wt% is lower than the modal proportion of ilmenite (ca. 50 wt%) in the ore body, implying accumulation of ilmenite and flotation of plagioclase. The fraction of residual liquid left after crystallization of Tellnes cumulates is estimated at 0.6 and the flotation of plagioclase at 26 wt% of the initial melt mass. The increasing content of intercumulus magnetite with stratigraphic height, from 0 to ca. 3 wt%, results from differentiation of the trapped liquid towards magnetite saturation. The MgO content of ilmenite (1.4–4.4 wt%) is much lower than the expected cumulus composition. It shows extensive postcumulus re-equilibration with trapped liquid and ferromagnesian silicates, correlated with distance to the host anorthosite. The Zr content of ilmenite, provided by in situ analyses, is low (<114 ppm) and uncorrelated with stratigraphy or Cr content. The data demonstrate that zircon coronas observed around ilmenite formed by subsolidus exsolution of ZrO₂ from ilmenite. The U-Pb zircon age of 920 ± 3 Ma probably records this exsolution process. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

赣中良山钼矿床流体包裹体特征及其地质意义

良山钼矿是近年来赣中地区新发现的钼矿,浅部矿体主要赋存于南华系浅变质岩系的构造裂隙中,矿石类型以含辉钼矿石英脉为主。流体包裹体岩相学和显微测温结果表明：含辉钼矿石英脉中的流体包裹体主要呈星散状随机或成群分布,其形态多样,大小集中在2~15 μm,包裹体的类型主要有纯液相包裹体、富气相两相包裹体、富液相两相包裹体和含液体CO₂三相包裹体4类,其中以富液相两相包裹体最为发育;包裹体的均一温度为136~298 ℃,盐度为1.22%~10.11%NaCleqv,密度为0.78~0.99 g/cm3,成矿流体属中-低温、低盐度、较低密度流体;成矿压力估算为13~70 MPa,形成深度为0.5~2.6 km。流体包裹体激光拉曼光谱分析表明：包裹体中气液相成分以H₂O为主,气相中还有少量的CO₂和CO。H、O、S同位素组成显示：成矿流体的δD值介于-61‰~-57.9‰,δ¹⁸OH₂O值介于-3.32‰~-0.52‰,具有岩浆水和大气降水混合的特征;成矿热液中的δ³⁴S值介于-1.8‰~+1.9‰,具有岩浆硫的特征。综合成矿地质特征及相关分析,认为成矿流体可能与燕山期的岩浆活动有关,属于岩浆热液流体,混合作用及钾化作用是促进金属富集沉淀成矿的主要因素,推测矿床属于岩浆热液充填石英脉型钼矿。     

Ore-forming Fluid Characteristics of the Saishitang Cu-polymetallic Deposit in Qinghai Province, China

Saishitang Cu-polymetallic deposit is located in the southeast section of Late Paleozoic arcfold in the southeastern margin of Qaidam platform. Accoring to the geological process of the deposit,four mineralization episodes were identified: melt/fluid coexisting period(O),skarn period(A),first sulfide period(B) and second sulfide period(C),and 10 stages were finally subdivided. Three types of inclusions were classified in seven stages,namely crystal bearing inclusions(type I),aqueous inclusions(type II) and pure liquid inclusions(type III). Type I and II inclusions were observed in stage O1,having homogenization temperature from 252 to 431°C,and salinities ranging from 24.3% to 48.0%. Type I inclusion was present in stage A1,having homogenization temperature from 506 to 548°C,and salinities ranging from 39.4% to 44.6%. In stage B1,type II and III inclusions were observed,with homogenization temperature concentrating between 300–400°C,and salinities from 0.4% to 4.3%. Type II inclusions were present in stage B2,with homogenization temperature varying from 403 to 550°C. In stage C1,type I and II inclusion commonly coexisted,and constituted a boiling inclusion group,having homogenization temperatures at 187–463°C,and salinities in a range of 29.4%–46.8% and 2.2%–11.0%. Type II and III inclusions were developed in stage C2,having homogenization temperature at 124–350°C,and salinities ranging between 1.6% and 15.4%. In stage C3,type II and III inclusions were presented,with a homogenization temperature range of 164–360°C,and salinities varying from 4.0% to 11.0%. The results of micro-thermal analysis show that fluids are characterized by high temperature and high salinity in stage O1 and A1,and experienced slight decrease in temperature and dramatic decrease in salinity in stage B1 and B2. In stage C1,the salinity of fluid increased greatly and a further decrease of temperature and salinity occurred in stage C2 and C3. Fluids boiled in stage C1. With calculated pressure of 22 MPa from the trapping temperature of 284–289°C,a mineralization depth of 2.2 km was inferred. Results of Laser Raman Spectroscopy show high density of H2 O,CH4 and CO2 were found as gas composition. H-O isotope study indicates the oreforming fluids were the mixture of magmatic water and meteoric water. Physicochemical parameters of fluids show oxygen and sulfur fugacity experienced a decrease,and redox state is weakly reducing. Along with fluid evolution,oxidation has increased slightly. Comprehensive analysis shows that melt exsolution occurred during the formation of quartz diorite and that metal elements existed and migrated in the form of chlorine complex. Immiscible fluid separation and boiling widely occurred after addition of new fluids,bringing about dissociation of chlorine-complex,resulting in a great deal of copper precipitation. In conclusion,Saishitang deposit,controlled by regional tectonics,is formed by metasomatism between highly fractionated mineralization rock body and wall rock,and belongs to banded skarn Cu-polymetallic deposit.     

193nmLA-ICPMS对国际地质标准参考物质中42种主量和微量元素的分析

本文采用配备有 193nm Ar F准分子 (excimer)激光器的 Geo L as2 0 0 M剥蚀系统和 Elan6 10 0 DRC ICP- MS对 4个美国地质调查所 (USGS)玻璃标准参考物质以及 3个美国国家标准技术研究院 (NIST)人工合成硅酸盐玻璃标准参考物质中几乎覆盖整个质量数范围 (从 7L i到 2 38U)的 38个微量和 4个主量 (Na、Mg、Ti和 Mn)元素进行了分析。分析结果表明 ,无论是对 USGS还是 NIST玻璃 ,元素分析的相对标准偏差 RSDs和分析值与参考值之间的相对偏差 (RDs)一般优于 10 % ,RSD和RD较大的元素主要出现在含量很低或不均匀样品中。稀土元素的 RSD显示 ,除 AGV- 2 G可能存在不均匀现象外 ,其它所测样品在 6 0 μm尺度上 ,元素分布是均匀的。本研究证明 ,由于 ICP- MS具有 10 8cps(每秒计数 )的动态线性范围 ,本实验室的L A- ICPMS系统可定量分析含量在百分之几的主量元素及微量元素。分析精密度和准确度可与常规溶液雾化进样 ICP- MS方法相媲美     

沉积物粒度分析方法的比较

近年来激光粒度分析法在沉积物粒度分析方面的应用得到了进一步扩展。本文利用美国麦克奇公司生产的S3500型激光粒度分析仪开展沉积物粒度分析方法实验,研究表明:S3500型仪器较优的样品用量约为0.2 g;稀释过程会影响样品的粒度分布;样品分取方式会带来不同的随机误差。与薄片图像法和筛析法两种传统粒度分析方法获得的粒度分布参数比较表明:激光法测得的平均粒径较薄片图像法和筛析法偏细;激光法和筛析法的峰度相关性较好。采用Malvern 2000和Micro S3500两种激光粒度分析仪测量结果的比较表明:Malvern 2000测得的平均粒径较Micro S3500测得的平均粒径偏细,但二者的相关性很好(r=0.9574),研究认为这两种粒度仪的测试结果会给岩石粒度定名带来差异。由于各种粒度分析方法存在差异和局限性,在实际工作中粒度分析应尽可能建立在同一测量体系上,以便资料对比。     

Airborne Laser Sensing of Scottish Coastal Waters

An Nd:YAG-based airborne lidar system has been used to measure the optical properties of littoral waters off the northwest Scottish coast. The small-scale structure of subsurface scattering layers was also investigated. Methods of solving the Lidar Sensing Equation in the single scattering approximation are described and the values of the derived extinction indices presented. The extinction index averaged over a series of five flights to the northeast of the Gulf Stream was k = 0.224 m -1 with a standard deviation of 0.212 m -1 . Further, it was demonstrated that, in coastal waters, optical inhomogeneities with dimensions between 50 m and 200 km obey the power law Sp k ~ k -P with the parameter P close to two. In turbid or transparent areas, the water extinction index can change by several tenths of a percent with respect to the surrounding water mass. This suggests that the observed nonmonotonic behavior of the power spectra of the water extinction index fluctuations is caused by the outer scale of turbulence, in particular, by the bottom depth at the measurement site.     

矿物激光显微光谱分析结果的热力学校正研究

由于激光蒸发和激发不同矿物的过程,都是从有序体系到无序体系的热力学转换过程,因此可以用矿物标准熵S°来考察分析精度.笔者提出了对初步分析分析结果Ci进行热力学校正,校正因子主要是相同取样量条件下的热力学参数Vg=S°/Vmol,实际取样量Vd,校正公式为Ct=Vgi·Vdi·Ci/Vgt·Vdt.实践表明,这一校正方法提高了矿物激光显微光谱分析精度.     

LTD500激光跟踪测量系统原理及应用

激光跟踪测量系统是瑞士徕卡公司生产的高精度工业测量仪器，它具有测量精度高，实时快速，动态测量，便于移动等优点。在航空航天，汽车制造，电子工业，高能粒子加速器工程以及大尺寸计算等行业中，均有广泛应用，随着我国上述行业测试计算的迅速发展，这类仪器已开始大量引进，如在沈飞，西飞，上飞及一些研究所已应用于生产实践，本文主要介绍激光跟踪仪的原理，校准方法及应用情况。     

浅谈地面三维激光扫描技术在市政工程测量中的应用

三维激光扫描技术,又称实景复制技术,是上世纪九十年代中期开始出现的一项高新技术,它通过高速激光扫描测量的方法,大面积高分辨率地快速获取被测对象表面的三维坐标数据,为快速建立物体的三维影像模型提供了一种全新的技术手段。简要介绍三维激光扫描数据采集和处理全过程,指出其优势和劣势,并探讨其在市政工程测量中的应用前景。     

The Carbonate Radical (HCO3·/CO3–·) as a Reactive Intermediate in Water Chemistry: Kinetics and Modelling

Results from kinetic laboratory studies of reactions of the carbonate radical anion (CO₃^–·) with aromatic compounds in aqueous solution at T = 298 K are presented. Data were obtained in using a laser photolysis laser long-path absorption (LP-LPLA) apparatus which was designed for direct time-resolved studies of radical reactions. For the reactions of CO₃^–· with hydroquinone dimethyl ether (2), methyl anisole (3), benzene (4), p-xylene (5), toluene (6), chlorobenzene (7), nitrobenzene (8), and benzonitrile (9), rate coefficients of k₂ = (3.0 ± 0.6)·10⁷ M^–1 s^–1, k₃ = (9.7 ± 1.7)·10⁵ M^–1 s^–1, k₄ = (3.2 ± 0.7)·10⁵ M^–1 s^–1, k₅ = (3.8 ± 0.9)·10⁴ M^–1 s^–1, k₆ = (6.8 ± 2.3)·10⁴ M^–1 s^–1, k₇ = (2.7 ± 0.6)·10⁵ M^–1 s^–1, k₈ = (1.4 ± 0.5)·10⁴ M^–1 s^–1, and k₉ < 1.3·10² M^–1 s^–1 were obtained. In further studies the effect of temperature on the reactions (2), (4), and (5) has been studied. The kinetic data obtained for the reaction of the carbonate radical anion with aromatic compounds were compared to the corresponding reactions of the hydroxyl radical. Finally, these kinetic data were used within a simple model system to investigate the implications of carbonate radical anion kinetics within water treatment processes. It is shown that the degradation of organic pollutants in ^·OH-radical based water treatment may proceed via the CO₃^–·/HCO_3· radical under certain conditions.