河南马超营—独树一带银铅锌成矿地质条件及找矿前景

马超营－独树一带位于华北陆块南缘，为一元古宙－古生代裂陷槽。官道口群、栾川群和陶湾群为滨海、浅海、陆棚相陆缘碎屑－碳酸盐岩沉积建造，强烈的浅源火山喷（气）发活动，形成多层硅质条带（团块）、硅质岩以及含Ag、Pb、Zn矿化的层状夕卡岩带。该带是比较典型的地球化学急变带与地球物理梯度带交叉区，壳、幔富含Mo、Pb、Zn、Au元素。基于该带银铅锌金矿成矿地质条件，推断具有良好的找矿前景。     

New ICP‐MS Results for Trace Elements in Five Iron‐Formation Reference Materials

Iron formations (IFs) typically contain low mass fractions of most trace elements, including the rare earth elements (REE), and few publications describe analytical methods dedicated to this matrix. In this study, we used bomb and table‐top acid dissolution procedures and ICP‐MS to determine the mass fractions of trace elements in IF reference materials FER‐1, FER‐2, FER‐3, FER‐4 and IF‐G. The full digestion of the IF samples with the bomb procedure required the addition of a small amount of water together with the acids. The results obtained by this method mostly agreed statistically with published values. The most remarkable exception was the higher values obtained for the heavy REE in FER‐3. The recoveries of the REE obtained with the table‐top procedure were slightly higher than those of the bomb digestion, except for the values of the heavy REE in FER‐3 and FER‐4, which were up to 30% lower than published values. Sintering of the samples with sodium peroxide was performed to determine the REE, but the results tended to be lower than those derived following acid digestion. On the whole, the recoveries showed dependence on the conditions of digestion, but subtle differences in trace mineral composition between samples also exerted influence on the analytical results for trace elements.     

Rapid Determination of Trace and Ultra Trace Level Elements in Diverse Silicate Rocks in Pressed Powder Pellet Targets by LA‐ICP‐MS using a Matrix‐Independent Protocol

A simple, single sample preparation involving pressed rock powder pellets was utilised to determine the trace and ultra trace abundances of petrogenetically important elements including high field‐strength elements and REEs by laser ablation‐ICP‐MS. One of the elements predetermined by XRF spectrometry served as an internal standard. The influence of sample preparation parameters (grain size, pellet compactness and amount of binding media) on analytical performance was also investigated, including sample homogeneity issues at the laser sampling scale. Line scanning with a high repetition frequency (20 Hz) and large beam diameter (200 μm) ensured ablation from a larger sample surface area, eliminating issues related to sample heterogeneity. A median grain size of about 10 μm for silicate rock powders was found to be sufficiently representative at this scale of laser sampling. Granitic rocks or samples containing resistant minerals such as zircon needed extra grinding to achieve grain sizes down to < 5 μm for better precision for elements that are concentrated in these phases. Using ¹³⁷Ba as an internal standard, reasonable accuracies within 15–20% for most of the high mass trace elements were achieved; in the case of low mass elements, it may deviate up to 40%. Precision of measurements rarely exceeded 15% RSD.     

Reference Values Following ISO Guidelines for Frequently Requested Rock Reference Materials

We present new reference values for nineteen USGS, GSJ and GIT‐IWG rock reference materials that belong to the most accessed samples of the GeoReM database. The determination of the reference values and their uncertainties at the 95% confidence level follows as closely as possible ISO guidelines and the Certification Protocol of the International Association of Geoanalysts. We used analytical data obtained by the state‐of‐the‐art techniques published mainly in the last 20 years and available in GeoReM. The data are grouped into four categories of different levels of metrological confidence, starting with isotope dilution mass spectrometry as a primary method. Data quality was checked by careful investigation of analytical procedures and by the application of the Horwitz function. As a result, we assign a new and more reliable set of reference values and respective uncertainties for major, minor and a large group of trace elements of the nineteen investigated rock reference materials.     

金川镍矿含矿岩体的稀土元素及微量元素地球化学特征

通过对采自金川镍矿I矿区露天矿的第二期侵入岩体中。样品的稀土元素、微量元素进行全岩等离子质谱（ICP－MS）测定发现第二期侵入的岩体具有明显的轻稀土元素富集和无明显铕异常的特征，是上地幔低比例平衡部分熔融和分离结晶共同作用的产物。岩体中镍黄铁矿、磁黄铁矿、黄铁矿成条带状出现，表明其形成时低氧逸度的成岩环境。     

A Comprehensive Method for Precise Determination of Re,Os, Ir,Ru, Pt,Pd Concentrations and Os Isotopic Compositions in Geological Samples

A comprehensive method for the precise determination of Re, Os, Ir, Ru, Pt and Pd concentrations as well as Os isotopic compositions in geological samples is presented. Samples were digested by the Carius tube method, and the Os was extracted by conventional CCl₄ method. The Re, Ir, Ru, Pt and Pd were first subgroup separated from the matrix elements into Re‐Ru, Ir‐Pt and Pd by a 2‐ml anion exchange column. Subsequently, the Re‐Ru was further purified by a secondary 0.25 ml anion exchange column or by microdistillation of Ru using CrO₃‐H₂SO₄ as an oxidant followed by a secondary 0.25 ml anion exchange separation of Re. The Pd and Ir‐Pt were further successively purified by an Eichrom‐LN column to completely remove Zr and Hf, respectively. Rhenium, Ir, Ru, Pt and Pd were individually measured by multi‐collector inductively coupled plasma‐mass spectrometry (MC‐ICP‐MS), except for Ru after microdistillation purification was analysed by negative‐thermal ionisation mass spectrometry (N‐TIMS). The analytical results for peridotite reference material WPR‐1 agree well with the previously published data. Finally, several mafic rock reference materials including TDB‐1, WGB‐1, BHVO‐2, BCR‐2, BIR‐1a and DNC‐1a were analysed for Re‐Os isotopes and platinum‐group element concentrations to test their suitability for certification.     

Palaeomagnetic,geochronological and geological constraints on the tectonic evolution of the Mejillones Peninsula,northern Chile

Palaeomagnetic and geochronological data from an Early Palaeozoic high grade metamorphic complex (Jorgina Formation) and Jurassic layered basic intrusion (Moreno Complex) are reported from the Mejillones Peninsula of northern Chile (23–23°30'S). ⁴⁰Ar–³⁹Ar dates from the Lower Palaeozoic Jorgina Formation and the Moreno Complex are between 170 and 158 Ma, coincident with a phase of emplacement of the north Chilean coastal batholith. This suggests that intrusion and magnetization of the Moreno Complex and the metamorphism and remagnetization of the Jorgina Formation were related to batholith emplacement. Extracted stable components of magnetization from all units (17 sites) define site-mean directions with a scattered distribution. The scatter in site-mean directions is interpreted as being due to minor, localized, non-uniform, block-fault related (normal or strike-slip, or both) rotation after 158 Ma. The palaeomagnetic and geochronological data indicate that no significant large-scale latitudinal translation of crustal blocks has taken place in this part of northern Chile since the Late Jurassic. In addition, they indicate that the uniform clockwise rotation after the mid-Cretaceous which affected the adjacent Cordillera de la Costa either did not extend into the Mejillones Peninsula or took the form of localized block-fault rotations. The restriction of palaeomagnetically defined styles of rotation to discrete areas within the north Chilean forearc indicates that forearc wide block-fault rotation models are not applicable to the Pacific margin of northern Chile.