黑龙江省嫩江县三矿沟Cu-Fe-Mo矿床岩浆岩成因研究

三矿沟Cu-Fe-Mo矿床是大兴安岭地区三矿沟—多宝山构造-成矿带中一个比较典型的矽卡岩型矿床。在大量野外地质调查、室内岩矿鉴定的基础上,对与成矿有关的三矿沟复式英云(花岗)闪长岩体的岩石地球化学特征进行了分析,探讨了该岩体的成因类型和构造环境。研究表明,该矿床岩浆岩体属于钙碱性I型花岗岩,具有大陆地壳的特征,形成于与造山花岗岩有关的火山弧环境或相似的构造环境中,主要与造山阶段的火山弧花岗岩关系密切。稀土元素配分图显示向右缓倾斜的轻稀土元素富集型特点,轻、重稀土分馏较为明显,无明显的负铕异常,暗示其具有相同或相近的成因,也反映了同源岩浆的特点。δEu值介于0.81~1.24,δCe值为1.00~1.13,表明岩浆演化过程中发生了微弱的分离结晶作用,同时又受到同化混染作用的一定影响,其成岩环境氧逸度较低,指示了缺氧环境,有利于金属元素的积聚而形成矿床。     

国际油气井钻头进展概述（二）——FuseTek融合钻头与Pexus组合钻头

NOV公司2013年向市场推出FuseTek融合钻头。它将PDC钻头的高钻速与孕镶金刚石钻头的耐磨性结合于一体,适宜于钻进中硬—坚硬、高研磨性地层。FuseTek钻头已广泛应用于刚果、厄瓜多尔、中国、哥伦比亚等国家。应用表明,该新型组合钻头比PDC钻头或牙轮钻头钻进效率提高许多,工作寿命增加1～3倍或更多。Shear Bits公司于2014年推出Pexus组合钻头。该钻头广泛应用于加拿大冰川冰碛物钻进。地层上部硬卵砾石层利用可转动硬质合金齿钻进,下部软砂岩与页岩则运用PDC碎岩。整个冰碛物地层用一个Pexus钻头一钻到底。所述3类组合式钻头（含Kymera钻头）对于未来实现“一个钻头,一口井”的目标有重要意义。     

Tracing the source of metals in Geogas from metal deposits in a loess-covered region北大核心CSCD

In order to test the distribution characteristics of metallogenic elements and the application effectiveness of the traee elements and REE for tracing the source of Geogas anomaly, the distribution characteristics of metallogenetic elements .trace elements and REE in different media of the Jiaolongzhang Pb-Zn deposit underneath the loess have been studied in this paper. Results indicate that the distribution characteristics of Geogas anomalous elements over the concealed orebodies are coincided with those of the enriched elements of ores, while the distribution characteristics of trace elements and REE in background Geogas samples are distinctly different from those of other media, indicating that the source of background Geogas materials is influenced by various factors( geological bodies, lab environment and blank reagent). The similar distribution characteristics of the trace elements in the Geogas samples of anomalous areas and in the ores suggested that Geogas anomaly is affected by concealed orebodies in depth. The difference between REE patterns of the Geogas samples of the anomalous area and those of other solid media might be caused by inadequate analytical precision and low collecting efficiency of the instrument. It is believed that the REE tracing method can provide the information on the source of Geogas anomaly if the analytical precision and collecting efficiency of REE could be constantly increased.     

Origin of the Breno and Esino dolomites in the western Southern Alps (Italy): Implications for a volcanic influence

The Esino Limestone of the western Southern Alps represents a differentiated Ladinian-Lower Carnian (?) carbonate platform comprised of margin, slope and peritidal inner platform facies up to 1000 m thick. A major regional subaerial exposure event lead to coverage by another peritidal Lower Carnian carbonate platform (Breno Formation). Multiphase dolomitization affected the carbonate sediments. Petrographic examinations identified at least three main generations of dolomites (D1, D2, and D3) that occur as both replacement and fracture-filling cements. These phases have crystal-size ranges of 3–35 μm (dolomicrite D1), 40–600 μm (eu-to subhedral crystals D2), and 200 μm to 5 mm (cavity- and fracture-filling anhedral to subhedral saddle dolomite D3), respectively.The fabric retentive near-micritic grain size coupled with low mean Sr concentration (76 ± 37 ppm) and estimated δ¹⁸O of the parent dolomitizing fluids of D1 suggest formation in shallow burial setting at temperature ∼ 45–50 °C with possible contributions from volcanic-related fluids (basinal fluids circulated in volcaniclastics or related to volcanic activity), which is consistent with its abnormally high Fe (4438 ± 4393 ppm) and Mn (1219 ± 1418 ppm) contents. The larger crystal sizes, homogenization temperatures (D2, 108 ± 9 °C; D3, 111 ± 14 °C) of primary two-phase fluid inclusions, and calculated salinity estimates (D2, 23 ± 2 eq wt% NaCl; D3, 20 ± 4 eq wt% NaCl) of D2 and D3 suggest that they formed at later stages under mid-to deeper burial settings at higher temperatures from dolomitizing fluids of higher salinity, which is supported by higher estimated δ¹⁸O values of their parent dolomitizing fluids. This is also consistent with their high Fe (4462 ± 4888 ppm; and 1091 ± 1183 ppm, respectively) and Mn (556 ± 289 ppm and 1091 ± 1183 ppm) contents, and low Sr concentrations (53 ± 31 ppm and 57 ± 24 ppm, respectively).The similarity in shale-normalized (SN) REE patterns and Ce (Ce/Ce*)_SN and La (Pr/Pr*)_SN anomalies of the investigated carbonates support the genetic relationship between the dolomite generations and their calcite precursor. Positive Eu anomalies, coupled with fluid-inclusion gas ratios (N₂/Ar, CO₂/CH₄, Ar/He), high F⁻ concentration, high F/Cl and high Cl/Br molar ratios suggest an origin from diagenetic fluids circulated through volcanic rocks, which is consistent with the co-occurrence of volcaniclastic lenses in the investigated sequence.     

A novel method to estimate mineral compositions of mudrocks: A case study for the Canadian unconventional petroleum systems

The mineral composition of mudrocks is an essential attribute in controlling the reservoir quality of unconventional petroleum systems. The present study introduces a semi-quantitative method to estimate mineral phases of mudrocks in various Canadian unconventional hydrocarbon systems using total elemental analysis (inductively coupled plasma-mass spectrometry (ICP-MS)) and Rock-Eval data (total organic carbon (TOC) and mineral carbon (MinC)).This method involves statistical analysis based on a sound knowledge of hydrocarbon source rock inorganic geochemistry. The workflow can be divided into four steps: (i) converting major elements (Si, Al, Fe, K, Na, Ca, Mg, Ti, and P) to their oxides, (ii) inferring modes of occurrence of elements using statistical analysis of geochemical data (major elements, TOC, and MinC), (iii) identifying the mineral types (oxide, aluminosilicates, carbonates, sulfide, and phosphate) according to elemental occurrences and calculating mineral phase concentrations, and (iv) verifying the results by comparing to XRD data on selected samples. The results, especially for brittle minerals such as quartz, carbonates (e.g. calcite, dolomite, and ankerite), and pyrite, show that the estimated mineral compositions correspond closely and consistently with measured mineralogy obtained from XRD. This method takes advantage of bulk geochemical data already available for hydrocarbon potential and chemostratigraphic studies, without devoting additional samples and cost for XRD analysis.     

长岛县南五岛土壤地球化学特征及环境质量评价

以长岛县南五岛土壤为研究对象,对区内土壤元素的含量特征进行分析,并对土壤环境质量进行评价。结果表明：研究区土壤平均含量与烟台市、山东省以及全国土壤平均水平相比,除CaO,Na2O,Hg,S,Se,P,F元素含量差异较明显,其他大部分元素含量相对稳定,元素含量的高低不仅与研究区背景条件有关,也与人类活动密切相关。研究区土壤环境质量整体较好,大部分区域属于清洁区和尚清洁区,仅城区局部受到一定程度的Cd,Hg,Zn污染。     

TRACE ELEMENT DISTRIBUTION AND IMPLICATIONS IN SEDIMENTS ACROSS THE ALLERØD–YOUNGER DRYAS BOUNDARY IN THE NETHERLANDS AND BELGIUM

In the Northern Hemisphere, the Younger Dryas cooling occurred between 12.8 and 11.7 ka bp . This cooling is thought to have been the result of an abrupt change in atmospheric and oceanic circulations. One of the hypotheses explaining such a change suggests that just before the onset of the Younger Dryas cooling, multiple airbursts/impacts occurred over the Northern Hemisphere. We studied the late Pleistocene sediments from the Netherlands and Belgium to check whether a sudden short event might have taken place just before the onset of the Younger Dryas cooling. The geochemical features revealed suggest that such events might have occurred. The presence of products of biomass burning is suggested on the basis of trace element features of sediments from the lower Younger Dryas boundary. The presence of a volcanic component and a component resulting from extensive biomass burning in the sediments of c. 12.9 ka bp are indicated on the basis of trace element features. The volcanic component may be related to the Laacher See volcano eruption, whereas the cause of the extensive biomass burning remains unclear.     

An Investigation of Digestion Methods for Trace Elements in Bauxite and Their Determination in Ten Bauxite Reference Materials Using Inductively Coupled Plasma‐Mass Spectrometry

Trace elements from samples of bauxite deposits can provide useful information relevant to the exploration of the ore‐forming process. Sample digestion is a fundamental and critical stage in the process of geochemical analysis, which enables the acquisition of accurate trace element data by ICP‐MS. However, the conventional bomb digestion method with HF/HNO₃ results in a significant loss of rare earth elements (REEs) due to the formation of insoluble AlF₃ precipitates during the digestion of bauxite samples. In this study, the digestion capability of the following methods was investigated: (a) ‘Mg‐addition’ bomb digestion, (b) NH₄HF₂ open vessel digestion and (c) NH₄F open vessel digestion. ‘Mg‐addition’ bomb digestion can effectively suppress the formation of AlF₃ and simultaneously ensure the complete decomposition of resistant minerals in bauxite samples. The addition of MgO to the bauxite samples resulted in (Mg + Ca)/Al ratios ≥ 1. However, adding a large amount of MgO leads to significant blank contamination for some transition elements (V, Cr, Ni and Zn). The NH₄HF₂ or NH₄F open vessel digestion methods can also completely digest resistant minerals in bauxite samples in a short period of time (5 hr). Unlike conventional bomb digestion with HF/HNO₃, the white precipitates and the semi‐transparent gels present in the NH₄HF₂ and NH₄F digestion methods could be efficiently dissolved by evaporation with HClO₄. Based on these three optimised digestion methods, thirty‐seven trace elements including REEs in ten bauxite reference materials (RMs) were determined by ICP‐MS. The data obtained showed excellent inter‐method reproducibility (agreement within 5% for REEs). The relative standard deviation (% RSD) for most elements was < 6%. The concentrations of trace elements in the ten bauxite RMs showed agreement with the limited certified (Li, V, Cr, Cu, Zn, Ga, Sr, Zr and Pb) and information values (Co, Ba, Ce and Hf) available. New trace element data for the ten RMs are provided, some of which for the first time.     

地质背景对土壤微量元素的影响——以渝北地区为例

研究地质背景对土壤元素的控制特征,可为区域土壤元素地球化学研究、种植施肥和农业布局提供科学依据。本研究利用网格化定位与化学分析的方法,结合GIS技术和相关评价标准,探讨了地质背景对Cl、Mn、B、Zn、Cu和Mo元素含量及分布的影响。结果表明:渝北地区土壤Mn、Cu、Zn元素含量整体处于适中与丰富水平,Mo、B元素丰缺参半;B、Mo元素含量显著高于重庆主城区,Zn元素含量显著高于全国水平。受地质背景影响,B、Cl、Cu、Mn元素呈现高度空间相关性,结构性空间变异起主导作用;Mo、Zn元素表现中等空间相关性,由结构性因素和随机因素双重控制。地层的组对元素含量分布起主控作用,土壤元素含量分布形状在空间上与地层组相对应。成土母岩决定土壤元素含量,是土壤元素含量水平的重要控制因素之一,其影响因素主要为岩石类型,其次为岩石形成的地质时期。土壤类型显著影响元素含量,总体上,Mn、Cu、Zn、Mo、B在石灰岩土中含量最高;除B、Mo元素外,其他元素在黄壤中含量最低。     

Petrology and PGE Abundances of High‐Cr and High‐Al Podiform Chromitites and Peridotites from the Bulqiza Ultramafic Massif,Eastern Mirdita Ophiolite,Albania

The Bulqiza ultramafic massif, which is part of the eastern Mirdita ophiolite of northern Albania, is world renowned for its high-Cr chromitite deposits. High-Cr chromitites hosted in the mantle section are the crystallized products of boninitic melts in a supra-subduction zone (SSZ). However, economically important high-Al chromitites are also present in massive dunite of the mantle-crust transition zone (MTZ). Chromian-spinel in the high-Al chromitites and dunites of the MTZ have much lower Cr# values (100Cr/(Cr+Al)) (47.7–55.1 and 46.5–51.7, respectively) than those in the high-Cr chromitites (78.2–80.4), harzburgites (72.6–77.9) and mantle dunites (79.4–84.3). The chemical differences in these two types of chromitites are reflected in the behaviors of their platinum-group elements (PGE). The high-Cr chromitites are rich in IPGE relative to PPGE with 0.10–0.45 PPGE/IPGE ratios, whereas the high-Al chromitites have relatively higher PPGE/IPGE ratios between 1.20 and 7.80. The calculated melts in equilibrium with the high-Cr chromitites are boninitic-like, and those associated with the high-Al chromitites are MORB-like but with hydrous, oxidized and TiO2-poor features. We propose that the coexistence of both types of chromitites in the Bulqiza ultramafic massif may indicates a change in magma composition from MORB-like to boninitic-like in a proto-forearc setting during subduction initiation.