A catalogue of major and trace element data for Icelandic Holocene silicic tephra layers

Tephra layers with Icelandic provenance have been identified across the North Atlantic region in terrestrial, lacustrine, marine and glacial environments. These tephra layers are used as marker horizons in tephrochronology including climate studies, archaeology and environmental change. The major element chemistries of 19 proximally deposited Holocene Icelandic silicic tephra layers confirm that individual volcanic systems have unique geochemical signatures and that eruptions from the same system can often be distinguished. In addition, glass trace element chemistry highlights subtle geochemical variations between tephra layers which appear to have identical major element chemistry and thus allows for the identification of some, if not all, tephra layers previously considered identical in composition. This paper catalogues the compositional variation between the widespread Holocene Icelandic silicic tephra deposits.     

Diel stream geochemistry,Taylor Valley,Antarctica

Unlike temperate and polythermal proglacial streams, the proglacial streams in Taylor Valley (TV), Antarctica, are derived primarily from glacier surface melt with no subglacial or groundwater additions. Solute responses to flow reflect only the interaction of glacial meltwater with the valley floor surrounding the stream channel. We have investigated the major, minor and trace element 24‐h variations of two proglacial melt streams, Andersen Creek and Canada Stream, originating from the Canada Glacier in TV, Antarctica. Both streams exhibited diel mid‐austral summer diurnal flow variation, with maximum flow being more than 50 times the minimum flow. Dissolved (< 0.4 µm) major, minor and trace solute behaviors through diel periods were strongly controlled by the availability of readily solubilized material on the valley floor and hyporheic‐biological exchanges. Anderson Creek had generally greater solute concentrations than Canada Stream because of its greater receipt of eolian sediment. Andersen Creek also acquired greater solute concentrations in the rising limb of the hydrograph than the falling limb because of dissolution of eolian material at the surface of the stream channel coupled with minimal hyporheic‐biological exchange. Conversely, Canada Stream had less available eolian sediment, but a greater hyporheic‐biological exchange, which preferentially removed trace and major solutes in the rising limb and released them in the falling limb. Given the dynamic nature of discharge, eolian, and hyporheic‐biological processes, solute loads in TV streams are difficult to predict. Copyright © 2012 John Wiley & Sons, Ltd.     

地理网格技术在产地溯源码编制中的应用研究

针对农产品溯源中溯源编码通用性差、不便于查询的问题,本文分析了国内外地理网格技术与产地溯源码的研究现状,并结合二维码技术,提出了基于地理网格技术的二维产地溯源码编制规则,详细介绍了产地溯源编码的组成,并以应用实例验证了编码的实用性与便捷性。     

Geochemistry of Paraná-Etendeka basalts from Misiones,Argentina: Some new insights into the petrogenesis of high-Ti continental flood basalts

The Early Cretaceous (∼135–131 Ma) Paraná-Etendeka continental flood basalts, preserved in bulk in the Paraná basin of southern Brazil and vicinity, have been divided into low-Ti and high-Ti types that govern the southern and northern halves of the basin, respectively. We have examined a new sample set from the southern margin of the northern high-Ti segment of Paraná basalts in Misiones, northeastern Argentina. These basalts are strongly to moderately enriched in TiO₂ (2–4 wt.%), have relatively high Ti/Y (300–500), low MgO (3.5–6.5 wt.%), and high Fe (FeO(tot) 12–14 wt.%) and belong to the Pitanga and Paranapanema magma types of Peate et al. (1992). Nd and Sr isotope compositions are quite unvarying with ε_Nd (at 133 Ma) values of −4.6 to −3.6 and initial ⁸⁷Sr/⁸⁶Sr of 0.7054–0.7059 and show no variation with fractionation. Compared to high-Ti lavas in the central and northern parts of the Paraná high-Ti basalt segment, the lavas from Misiones are similar to those in the northeastern magin of the basin but less radiogenic in initial Nd isotope composition than those in the central part. This variation probably reflects mixed EM1-EM2 source components in the sublithospheric mantle. A polybaric melt model of a sublithospheric mantle source at the garnet lherzolite-spinel lherzolite transition is compatible with the observed Ti budget of the Pitanga and Paranapanema lavas, regardless of the Nd isotope composition of their purported source.     

陕县宽坪银多金属矿区地质特征与成矿规律

陕县宽坪银多金属矿位于崤山矿集区内,已探明银铅锌储量达中等以上规模。通过研究矿区地质特征,认为矿体主要受构造蚀变带控制,在含矿热液的多期、多阶段交代和充填作用下,在构造有利部位富集成矿。     

湖南湘潭锰矿的地球化学特征及成矿机制

湘潭锰矿床的锰矿层赋存于新元古代南华系(成冰系)大塘坡组底部含锰黑色页岩中,含锰矿物主要为菱锰矿。湘潭锰矿的Fe/Mn值低,Th/U、V/(V+Ni)和V/Cr值等地球化学指标显示其发育在氧化-次氧化的沉积环境中,暗示菱锰矿并不是由Mn~(2+)和CO_3~(2-)直接沉淀形成的。湘潭锰矿稀土元素含量高,稀土元素配分模式存在轻微的中稀土元素富集,具有明显的Ce正异常,这些特征指示湘潭锰矿含锰矿物是以锰氧化物或氢氧化物的形式沉淀的。同时,锰矿的碳同位素富集碳的轻同位素,说明有机物参与了菱锰矿的形成过程。综合分析表明,湘潭锰矿成矿过程可以分为沉淀和转化两个阶段:在氧化性的水体中,Mn以氧化物或氢氧化物的形式沉淀;在缺氧且富含有机物质的成岩环境中,Mn氧化物或氢氧化物被有机物还原而转化生成菱锰矿。这与华南地区其他几个典型的大塘坡式锰矿的成矿机制一致。     

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。     

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.     

济宁许厂煤矿伴生分散元素铼的富集成矿探析

铼是一种分散金属,目前尚没有在煤层中富集成矿的案例。该文依据山东省济宁煤田许厂煤矿16上、17煤层光谱分析成果,结合铼元素的性质、物质来源和石炭-二叠纪太原组的聚煤环境等因素进行综合分析,论证了其富集可能性。简要阐述了铼富集成矿的意义,建议煤田地质勘查工作中加强对煤中伴生铼元素的分析和研究。     

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.