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.     

无内标-多外标校正激光剥蚀等离子体质谱法测定磁铁矿微量元素组成

激光剥蚀电感耦合等离子体质谱(LA-ICP-MS)常用于磁铁矿原位微量元素分析,按照校正策略不同,主要分为内标法和无内标法。内标法需要用电子探针(EMPA)预先测定磁铁矿中内标元素Fe的含量,过程较繁琐,且待测元素含量会受到内标元素含量测定的影响。本文采用铁含量较高的玄武质玻璃BCR-2G、BIR-1G、BHVO-2G和GSE-1G作为外标,避免了内标元素含量的测定,建立了无内标-多外标校正LA-ICP-MS测定磁铁矿微量元素组成的分析方法。利用该方法测定了科马提岩玻璃GOR-128g和自然岩浆磁铁矿BC 28的微量元素组成以评估方法的可靠性。结果表明,科马提岩玻璃的测定结果与推荐值及前人内标法的测定值一致,多数元素的相对标准偏差RSD5%;自然岩浆磁铁矿的测定结果与推荐值相比,多数元素的RSD7%,低于前人内标法的RSD(15%)。由此说明无内标-多外标法可以实现富铁硅酸岩或磁铁矿微量元素含量的准确校正,克服了基体效应的影响。因此,无内标-多外标法是一种原位测定磁铁矿微量元素含量的快速、准确方法,具有一定的应用潜力。     

思维导图方法的教学实践

思维导图在国内外已有多项研究证明思维导图在促进学生创新思维发展上有作用。在测绘类学科的高校教学中引入思维导图这种学习和工作方法,用在测绘本科教学改革中的讲座责任制授课模式上,通过在测绘本科教学方法改革的需求分析、应用实践和学生调查统计,得出结论:思维导图用于测绘类高校教学中,有利于提高学生创新思辨和自主学习能力,有助于达到以"能力"为核心的测绘专业人才培养目标。     

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。     

高压超高压变泥质岩适用的地质温压计评述

高压超高压变泥质岩形成温压条件及p-T演化轨迹是高压超高压变质作用研究的重要内容。本文介绍了高压超高压变泥质岩适用的几种地质温压计,包括石榴子石-多硅白云母Fe~(2+)-Mg交换温度计、石榴子石-绿泥石Fe~(2+)-Mg交换温度计、硬绿泥石-绿泥石Fe~(2+)-Mg交换温度计、多硅白云母Si含量压力计、金红石Zr含量温度计、榍石Zr含量温压计、锆石Ti含量温度计、石英Ti含量温度计以及氧同位素温度计,并对上述温压计的适用条件及使用时的注意事项做了简要评述。     

熔融制样-X射线荧光光谱法测定电气石中12种主次量元素

电气石是一类含硼的铝硅酸盐矿物,化学成分复杂、化学稳定性强,不易湿法分解,B_2O_3含量较高,导致其主次量元素的同时测定存在一定困难。本文采用熔融法制样,建立了X射线荧光光谱法测定电气石Na_2O、MgO、Al_2O_3、SiO_2、P_2O_5、K_2O、CaO、TiO_2、V_2O_5、Cr_2O_3、MnO、TFe_2O_3等主次量元素的分析方法。样品与四硼酸锂-偏硼酸锂-氟化锂(质量比为4.5∶1∶0.4)混合熔剂的稀释比例为1∶10,消除了粒度效应和矿物效应;在缺少电气石标准物质的情况下,选择土壤、水系沉积物及多种类型的地质标准物质绘制校准曲线,利用含量与电气石类似的标准物质验证准确度,测定结果的相对标准偏差小于4.2%。采用所建方法测定四种不同类型电气石实际样品,测定值与经典化学法基本吻合。本方法解决了电气石不易湿法分解和硼的干扰问题,测定结果准确可靠,与其他方法相比操作简便,分析周期短。     

微波等离子体原子发射光谱法测定偏远矿区海泡石中的主微量元素

海泡石是具有层状结构的含水富镁硅酸盐黏土矿物,其中无机元素含量是揭示其成矿物质来源、成矿流体性质和矿床成因的重要依据,通常采用电感耦合等离子体发射光谱/质谱法(ICP-OES/MS)进行测定,等离子体(ICP)的高温激发会产生成大量谱线干扰,维持ICP稳定工作需使用高纯氩气,持续供气对于偏远矿区海泡石的检测还将面对气体采购和运输不便的问题。本文基于微波等离子体原子发射光谱(MP-AES)的低温激发技术减少光谱干扰,建立了准确测定偏远矿区海泡石中主量元素Mg、Al、Ca、Fe、K、Na和微量元素Cu、Zn、Mn、Pb含量的分析方法。利用硝酸-盐酸-氢氟酸混合酸对海泡石进行微波消解,避免了样品处理过程中分析元素的损失,加快了样品处理速度,同时提高了样品溶液的稳定性。通过选择各元素光谱线的分析波长,并利用快速线性干扰校正(FLIC)技术校正光谱干扰,以Lu为内标元素校正基体效应,提高了灵敏度和准确度。各元素的检出限为0.19～14.6μg/L。海泡石国家标准物质(GBW07138)各元素测定值与认定值的相对误差在-5.0%～6.7%之间。本方法具有检出限低、线性范围宽、结果准确等优点;MP-AES采用自带的氮气发生器为等离子体提供氮气作为工作气,无需引入复杂气体,提高了分析效率,尤其适用于气体采购和运输不便的偏远矿区。     

Fresh snow chemistry from high mountain regions in central himalayas

Investigations of atmospheric composition in the Himalayas has been limited in both temporal and spatial scales, mainly due to difficult logistics. Ideal sites for monitoring atmospheric composition and its evolution should be free from local pollution and representative of the remote troposphere (HUEBERT et al., 1980). As the Himalayas are far removed from highly industrialized regions they provide suitable locations to monitor the chemistry of the remote troposphere and to study the evolu…     

全球主要河流流域碳酸盐岩风化碳汇评估

碳酸盐岩风化吸收的大气CO₂主要以HCO₃ ^-形式连续地经由河流从大陆输送到海洋,成为陆地生态系统的重要碳汇。目前主要河流流域的碳酸盐岩风化碳汇估算存在不确定性,分布格局尚不清晰。基于GEMS-GLORI全球河流数据库提供的全球10万km ²以上主要河流流域多年平均监测数据,利用水化学径流法估算出全球主要河流流域碳酸盐岩对CO₂的吸收速率为0.43±0.15 Pg CO₂ yr ^-1,平均CO₂吸收通量为7.93±2.8 t km ^-2 yr ^-1。CO₂吸收通量在不同气候带下差异显著,热带和暖温带CO₂年吸收速率占全球主要河流流域年吸收速率的62.95%。冷温带CO₂年吸收速率占全球主要河流流域的33.05%,仅次于热带地区。本文划分出全球CO₂吸收通量的9个关键带,关键带的交汇处CO₂吸收通量较高。喀斯特出露流域碳酸盐岩对CO₂吸收通量的均值为8.50 t km ^-2 yr ^-1,约为非喀斯特流域的3倍。全球喀斯特出露流域碳酸盐岩风化碳汇在全球碳循环、水循环及碳收支平衡估算研究方面占据重要地位。