刘家峡水库表层沉积物微量元素地球化学特征

采用多元统计的方法对刘家峡水库表层沉积物中25种微量元素的含量、相关性、来源及控制因素进行了分析。结果显示:研究区表层沉积物中Sr、Zn、Zr和Ba的含量平均值超过了170μg/g,Cd、Mo和Tl的含量平均值都在1μg/g以下,其它元素含量平均值则在2. 01~104. 34μg/g。元素Cu、V、Co、Cr、Ni、Rb、Li、Cd、Be、Pb、Sc、As、Ga、Nb、Sn、Cs、Tl、Th和Al2O3等存在较为明显的相关性,且它们分布规律基本相似。因子分析表明,水库中微量元素分为3个主要来源,第一组分的元素分布受控于矿物岩石的自然风化剥蚀,其贡献率为63. 20%;第二组分的Zr和Ba主要受河流沉积物中元素的迁移和转化的影响,其贡献率为12. 51%;第三组分的Sr则主要受控于生物成因,其贡献率为9. 76%。另外,研究区重金属元素中,Zn和As含量远超过了全球页岩平均值,值得进一步的深入研究。     

中子活化法研究印度洋深海岩心中26种元素的某些地球化学行为

用中子活化分析法研究了一组印度洋深海钻孔样品中的26种元素地球化学行为，这些元素是Fc，Co、Cr、Na、K、Rb、Cs、Ca、Sr、Ba、U、Th、La、Ce、Nd、Sm、Eu、Tb、Yb、Lu、Zr、Hf、Sb，Ta、Sc和Au，给出了它们的浓度垂直分布特征，表现为典型的深海碳酸盐型沉积物，并讨论了它们的富集系数和停留时间。     

滇西北羊拉铜矿床里农—路农接合段构造地球化学与找矿预测

羊拉铜矿床是金沙江构造带内的代表性铜矿床,其矿体产出明显受到断裂及层间破碎带控制。本文重点对羊拉矿床里农—路农接合段的3450 m中段进行了构造地球化学研究,R型聚类分析和因子分析表明:该中段断裂构造岩微量元素主要表现为地层岩石微量元素组合(Nb、Hf、Ta、Zr、Rb、V、Sc、Th、Cs、Be、Ga、Li、REE、Ba、Cr、U、Co、Tl、Ge、(Ag、In、Sn、Cu)),中-高温成矿元素组合(Cd、Pb、Bi、Ag、As、Sn、In、Sb、Cu、Zn、Ge、Tl、Mo、U、(Co、Ga))和地质意义不明元素组合(Ni、Sr),揭示羊拉矿床的形成可能经历了成矿前期成矿元素的初步富集和成矿期退夕卡岩化过程中成矿元素的沉淀成矿。构造地球化学异常的分布则指示了找矿预测靶区。     

广西373铀矿床微量元素地球化学特征及其成因探讨

373铀矿床是我国南方典型碳硅泥岩型铀矿床之一,主要发育一套黑色弱硅化泥岩、粉砂岩,硅化生屑灰岩及其过渡型岩类地层,矿床明显受断裂发育影响,铀矿化于次级断裂带中.通过系统地球化学研究表明:3组不同期次脉体普遍亏损过渡元素Ti、Sc、Cr、Cu、Zn和高场强元素Nb、Ta、Zr和Hf;相对较富集Mn、Ni、As、Sr、Mo、Sb、Tl和U等微量元素.后期热液活动使脉体Ba、Sb、As和Mo等元素异常富集.后期热液叠加改造,使得岩石普遍亏损过渡元素Sc、Ti、Cr和高场强元素Nb、Ta、Zr、Hf,普遍富集Co、Ni、Zn、As、Sb、Mo、Cd、W、Tl、Pb、Bi和U,其中As、Sb、Mo、Tl和U尤为富集,富集系数平均达到100左右,U与W、As、Sb和Pb相关系数都在0.9左右,具有高度同源性,铀成矿与热液活动有关.典型剖面微量元素富集与硅化密切相关,当硅化达到一定程度后微量元素富集出现反转,即随着硅化强度增加而富集能力反而降低.V/Cr、V/Sc、Ni/Co、V/(V+Ni)、U/Th、δU、δEu和δCe等特征元素比值反应铀预富集形成于缺氧的古海洋环境.高丰度的As、Sb和Ba等元素,以及U-Th关系图解和Zn-Ni-Co三元图解均显示热水沉积成因.微量元素特征表明碳硅泥岩形成于缺氧的还原环境,铀预富集与热水沉积有关,铀成矿与热液叠加改造有关,后期热液沿运移通道上升进入储集空间,与铀预富集地层热液叠加成矿.     

封闭压力酸溶-盐酸提取-电感耦合等离子体质谱法测定地质样品中的多元素

高温、高压封闭压力酸溶可有效分解岩石、土壤、沉积物等地质样品,采用电感耦合等离子体质谱法(ICP-MS)进行测定,大部分元素可得到满意的回收率;但Zr、Hf、REEs、Rb、Th、U等元素用硝酸复溶困难,测定结果不准确。本文对传统的封闭压力酸溶方法进行改进,用盐酸复溶提取代替硝酸复溶提取,ICP-MS法测定岩石、土壤、沉积物等国家一级标准物质中Li、Be、Cr、Mn、Co、Ni、Cu、Zn、Ga、Rb、Sr、Mo、Cd、In、Cs、Ba、Ti、Zr、Nb、Sn、Sb、W、Hf、Ta、Tl、Pb、Bi、Th、U以及稀土元素(REEs)等46个元素。将原方法中的称样量25 mg加大至100 mg,溶样时间由12 h延长至48 h,有效地解决了取样代表性及HNO3复溶提取时Rb、Sr、REEs等元素测定结果偏低的问题。分析结果表明,除元素As和V在电感耦合等离子体质谱测定中存在Cl的干扰不能准确测定之外,其他44个元素的测定值与标准值基本一致。改进后的方法测定下限为0.01～0.85μg/g,精密度(RSD,n=10)为0.73%～13.1%,准确度小于<10%。方法准确、可靠,适用于各种不同种类地质样品的分析。     

珠江口海域与南黄海海域表层沉积物地球化学特征

对珠江口和南黄海近海海域10个站位的表层沉积物中67种元素进行分析,试图揭示两海域近海表层沉积物中主要元素的地球化学特征,包括分布特征及其控制因素,并通过两海域元素地球化学特征,初步探讨近海沉积环境特征。通过总结两海域表层沉积物中元素含量及分布特征,可以发现,近海海域总体上以陆源沉积为主,除Ca和Sr之外,大多数元素表现出明显的亲陆性。珠江口海域和南黄海海域沉积物元素含量的对比研究显示,前者相对富集As、Cd、Hg、Sb、Sr、Ca、Rb、C,后者相对富集Al2O3、Zr、Hf、Sc、Rb、Ga、Cs、V、Co、Cr、Cu、Mn、Ni、K2O、Na2O、B、Ba、I等。与上地壳相比,Ag、As、Bi、Hg、Li、N、Pb、Sb、Se、Cl、Br、I在两海域表层沉积物中均发生明显富集;Mo、Sn均呈现分散趋势;Sr、CaO在南黄海海域明显贫化,K2O、Na2O、Ba则在珠江口海域表现出贫化;其他元素与上地壳元素丰度相近。     

四川省癌死亡率与土壤环境中化学元素的关系

利用中国癌死亡率与土壤坏境中化学元素的相关性成果，研究了四川省癌死亡率与土壤环境中化学元素：As、Cd、Co、Cu、Hg、Mn、Ni、Pb、Se、V、Li、Na、K、Rb、Cs、Mg、Ca、Sr、Ba、B、Al、Ga、In、Tl、Sc、Y、La、Ce、Pr、Nd、Tb、Dy、Ho、Er、Tm、Yb、Lu、Th、U、Sn、Ti、Zr、Hf、Sb、Bi、Ta、Te、Mo、W、Br、I、Fe等52个元素含量的关系     

373铀矿床微量元素地球化学特征及其成因探讨

内容提要 373铀矿床是我国南方典型碳硅泥岩型铀矿床之一,主要发育一套黑色弱硅化泥岩、粉砂岩,硅化生屑灰岩及其过渡型岩类地层,矿床明显受断裂发育影响,铀矿化于次级断裂带中。通过系统地球化学研究表明：三组不同期次脉体普遍亏损过渡元素Ti、Sc、Cr、Cu、Zn和高场强元素Nb、Ta、Zr和Hf;相对较富集Mn、Ni、As、Sr、Mo、Sb、Tl和U等微量元素。后期热液活动使脉体Ba、Sb、As和Mo等元素异常富集。后期热液叠加改造,使得岩石普遍亏损过渡元素Sc、Ti、Cr和高场强元素Nb、Ta、Zr、Hf,普遍富集Co、Ni、Zn、As、Sb、Mo、Cd、W、Tl、Pb、Bi和U,其中As、Sb、Mo、Tl和 U尤为富集,富集系数平均达到100左右,U与W、As、Sb和Pb相关系数都在0.9左右,具有高度同源性,铀成矿与热液活动有关。典型剖面微量元素富集与硅化密切相关,当硅化达到一定程度后微量元素富集出现反转,即随着硅化强度增加而富集能力反而降低。V/Cr、V/Sc、Ni/Co、V/(V+Ni)、U/Th、δU、δEu和δCe等特征元素比值反应铀预富集形成于缺氧的古海洋环境。高丰度的As、Sb和Ba等元素,以及U-Th关系图解和Zn-Ni-Co三元图解均显示热水沉积成因。微量元素特征表明碳硅泥岩形成于缺氧的还原环境,铀预富集与热水沉积有关,铀成矿与热液叠加改造有关,后期热液沿运移通道上升进入储集空间,与铀预富集地层热液叠加成矿。     

吉林白山地区原煤微量元素地球化学特征

对吉林白山地区煤矿主采煤层中的As、B、Ba、Cd、Cu、Hg、Pb、Se、Sr等微量元素进行了分析,结果表明:太原组与山西组由于成煤环境不同,微量元素组成及其质量分数存在一定的差异,太原组原煤中As、B、Hg、Pb、Se、Zn的质量分数明显高于山西组,山西组原煤中Ba、Cr、Cu、Mn、V的质量分数明显高于太原组。白山地区原煤中As、B、Hg、Pb、Se的质量分数明显高于地壳元素平均值,呈富集状态;Co、Cd与地壳平均值接近,其他元素均亏损。与全国煤中微量元素的质量分数平均值相比,As、Ba、Co、Cr、Cu、Hg、Ni、Pb、Se、V、Zn的质量分数高于全国平均值。B、Mn、Sr质量分数低于全国平均值。微量元素赋存状态及相关分析表明,Fe与亲硫有害元素As、Cu、Hg、Pb、Se具有显著相关关系,说明煤中黄铁矿及其他硫化物是许多有害微量元素的重要载体。      

湘江湘潭段河岸沉积物重金属污染地球化学分析

本研究用X射线荧光(XRF)和电感耦合等离子质谱仪(ICP-MS)等对湘江湘潭段河岸沉积物进行了主元素、微量元素地球化学分析。结果表明,河岸沉积物具明显贫Na_2O、CaO、Mg O等碱质,而富Fe_2O_3、MnO等氧化物的化学组成特征。沉积物明显富集Cu、Pb、Zn、Mn、V、Cr、U、Th等多种重金属和Zr、Hf、Ta等高强场元素,而亲石元素Cs、Ga、Ge、Rb、Sr等及稀土元素(REE+Y)在沉积物中富集不明显。地累积系数(Igeo)法评价显示,河岸沉积物存在Cu、Zn、Pb等元素组成的潜在重金属污染。主元素与重金属元素相关性分析显示,Ba、Rb、Th、U、Sc、Cr、Ta、Nb、Zr、Hf、Ga、Ge、Y等主要赋存于石英等碎屑矿物中,这些微量金属元素可能主要为自然来源,在沉积物中化学性质相对稳定;而Mn、V、Co、Cr、Cu、Pb、Zn等重金属元素则主要赋存于铁、锰氧化物矿物相中,这些重金属元素可能以人为源为主,在沉积物中有一定的化学活性,可发生活化迁移。沉积物的Fe_2O_3、LOI、∑REE等的含量值及Eu/Eu*值可作为指示沉积物重金属污染的地球化学指标,对沉积物重金属污染有一定的指示作用。     

Neutron activation studies of the geochemical behaviours of 26 elements in deep-sea drill core sediments from the Indian Ocean

The geochemical behaviours of 26 elements in deep-sea drill core sediments from the Indian Ocean have been investigated with INAA, including Na, K, Ca, Sc, Cr, Fe, Co, Rb, Sr, Zr, Sb, Cs, Ba, La, Ce, Nd, Sm, Eu, Tb, Yb, Lu, Hf, Ta, Au, Th and U. Their distribution patterns with depth are also discussed. In terms of the enrichment factors of the respective elements, their residence times in the sea have been calculated by the least squares fitting and are compared with the previous results.     

Comparative geochemistry of shell phosphorites and dictyonema shales of the Baltic

Major and trace element composition of the Ordovician Obolus phosphorites and associated Dictyonema shales were determined by ICP-MS and chemical and microchemical elemental analyses. Relative to the phosphorites, the Dictyonema shales are substantially enriched in a variety of trace elements, except for As, Be, Co, Y, REE, Sr, and Pb. The Obolus phosphorites show enrichment of As, Bi, Hg, Mo, La, Y, Pb, and Sr and depletion of Ag, Ba, Be, Cd, Cr, Cu, Hf, Ni, Sc, Sn, U, V, Zn, and Zr relative to the world average phosphorite composition. The average trace element composition of the Dictyonema shales is close to the mean shale composition, except for higher contents of Mo, Hg, Pb, Se, Ta, Te, Th, V, and U and lower contents of Ba, Bi, Cd, Co, Re, Sr, and Zn. The results suggest that the change from phosphate sedimentation in aerated environments to anoxic carbonaceous sedimentation was accompanied by changes in the composition and concentration of trace elements in the sediment. Both facies show similar trends of trace element distribution indicative of the stability of the composition of seawater and terrigenous sediment input.     

XRF AND INAA DETERMINATIONS OF MAJOR AND TRACE ELEMENTS IN GEOLOGICAL SURVEY OF JAPAN IGNEOUS AND SEDIMENTARY ROCK STANDARDS

Major and trace element analyses have been obtained by wavelength dispersive X-ray fluorescence for the Geological Survey of Japan Igneous rock series and selected samples from the Sedimentary rock series reference samples. Additional trace element data for the Igneous rock series were obtained by instrumental neutron activation analysis. Samples were analyzed multiple times for 10 major elements (with loss-on-ignition) and the following trace elements; As, Ba, Ce, Co, Cr, Cs, Cu, Eu, Ga, Hf, La, Lu, Nb, Nd, Ni, Pb, Rb, Sb, Sc, Sm, Sr, Ta, Tb, Th, U, V, W, Y, Yb, Zn and Zr.     

Trace elements in the Goze Delchev coal deposit, Bulgaria

The geochemistry of trace elements in the underground and open-pit mine of the Goze Delchev subbituminous coal deposit have been studied. The coals in both mines are highly enriched in W, Ge and Be, and at less extent in As, Mn and Y as compared with the world-wide Clarkes for subbituminous coals. Ni and Ti are also enhanced in the underground coals, and Zr, Cr and Mo in the open-pit mine coals.Characteristic for the trace element contents in the deposit is a regular variation with depth. The following patterns were distinguished for profile I: a — the element content decreases from the bottom to the top of the bed paralleling ash distribution (Fe, Co, As, Sb, V, Y, Mo, Cs, REE, Hf, Ta, Th, P and Au); b — Ge and W are enriched in the near-bottom and near-top coals; c — in the middle part of the bed the content of K and Rb is maximal, while that of U is slightly enriched; d — Ba content decreases from the top to the bottom of the bed. In profile II, W and Be contents decrease from the bottom to the top. The near-bottom, and especially the near-roof samples of profile IV are highly enriched in Ge, while for W the highest is the content of the near-bottom sample.Ge, Be, As, Mn, Cl and Br are mainly organically associated. The organic affiliation is still strong for Co, B, Sr, Ba, Sb, U, Th, Mo, La, Ce, Sm, Tb and Yb in the underground coals, and Fe, Co, Na, W, Sr, Y and Ag in the coals from the open-pit mine. K, Rb, Ti, Zr, Hf and Ta are of dominant inorganic affinity. The chalcophile and siderophile elements correlate positively with Fe and each other and may be bound partly with pyrite or other sulphides and iron containing minerals.Compared statistically by the t-criteria, the elements Na, Li, Cu, Zn, Pb, Cr, Ni, Co, Mo, Fe and Be are of higher content in the open-pit mine. Tungsten is the only element of higher concentration in the underground mine. The contents of Ge, As, Sr, V, Mn, Y, Zr and P are not statistically different in both mines.It was supposed that there were multiple sources of the trace elements in the deposit. The source of the highly enriched elements (W, Ge, Be, and As) most probably were the thermal waters in the source area. The contemporary mineral springs are of high content of these elements. Another source were the hosting Mesta volcanic rocks, which are enriched in Sb, Mo, Hf, U, Th, As, Li and Rb. Some of the volcanics were hydrothermally altered and enriched or depleted of many elements. Thus, the hydrothermal solutions were also suppliers of elements for the coals. It is obvious that the contents, distribution and paragenesis, of the trace elements in both Goze Delchev coals reflect the geochemical specialization of the source area, including rocks, paleo- and contemporary thermal waters.     

Pedo-geochemical baseline content levels and soil quality reference values of trace elements in soils from the Mediterranean (Castilla La Mancha, Spain)

To evaluate trace element soil contamination, geochemical baseline contents and reference values need to be established. Pedo-geochemical baseline levels of trace elements in 72 soil samples of 24 soil profiles from the Mediterranean, Castilla La Mancha, are assessed and soil quality reference values are calculated. Reference value contents (in mg kg^?1) were: Sc 50.8; V 123.2; Cr 113.4; Co 20.8; Ni 42.6; Cu 27.0; Zn 86.5; Ga 26.7; Ge 1.3; As 16.7; Se 1.4; Br 20.1; Rb 234.7; Sr 1868.4; Y 38.3; Zr 413.1; Nb 18.7; Mo 2.0; Ag 7.8; Cd 4.4; Sn 8.7; Sb 5.7; I 25.4; Cs 14.2; Ba 1049.3; La 348.4; Ce 97.9; Nd 40.1; Sm 10.7; Yb 4.2; Hf 10.0; Ta 4.0; W 5.5; Tl 2.3; Pb 44.2; Bi 2.2; Th 21.6; U 10.3. The contents obtained for some elements are below or close to the detection limit: Co, Ge, Se, Mo, Ag, Cd, Sb, Yb, Hf, Ta, W, Tl and Bi. The element content ranges (the maximum value minus the minimum value) are: Sc 55.0, V 196.0, Cr 346.0, Co 64.4, Ni 188.7, Cu 49.5, Zn 102.3, Ga 28.7, Ge 1.5, As 26.4, Se 0.9, Br 33.0 Rb 432.7, Sr 3372.6, Y 39.8, Zr 523.2, Nb 59.7, Mo 3.9, Ag 10.1, Cd 1.8, Sn 75.2, Sb 9.9, I 68.0, Cs 17.6, Ba 1394.9, La 51.3, Ce 93.5, Nd 52.5, Sm 11.2, Yb 4.2, Hf 11.3, Ta 6.3, W 5.2, Tl 2.1, Pb 96.4, Bi 3.0, Th 24.4, U 16.4 (in mg kg^?1). The spatial distribution of the elements was affected mainly by the nature of the bedrock and by pedological processes. The upper limit of expected background variation for each trace element in the soil is documented, as is its range as a criterion for evaluating which sites may require decontamination.     

Effects of alteration on element distributions in archean tholeiites from the Barberton greenstone belt,South Africa

Major and trace element and modal analyses are presented for unaltered, epidotized, and carbonated tholeiite flows from the Barberton greenstone belt. Au, As, Sb, Sr, Fe⁺³, Ca, Br, Ga, and U are enriched and H₂O, Na, Mg, Fe⁺², K, Rb, Ba, Si, Ti, P, Ni, Cs, Zn, Nb, Cu, Zr, and Co are depleted during epidotization. CO₂, H₂O, Fe⁺², Ti, Zn, Y, Nb, Ga, Ta, and light REE are enriched and Na, Sr, Cr, Ba, Fe⁺³, Ca, Cs, Sb, Au, Mn, and U are depleted during carbonization-chloritization. The elements least affected by epidotization are Hf, Ta, Sc, Cr, Th, and REE; those least affected by carbonization-chloritization are Hf, Ni, Co, Zr, Th, and heavy REE. Both alteration processes can significantly change major element concentrations (and ratios) and hence caution should be used in distinguishing tholeiites from komatiites based on major elements alone. The amount of variation of many of the least mobile trace elements in the altered flows is approximately the same as allowed by magma model calculations. Hence, up to about 10% carbonization and 60% epidotization of tholeiite do not appreciably affect the interpretation of trace-element models for magma generation.     

Chemistry of Aerosols over Chukchi Sea and Bering Sea

The contents of elements in aerosols sampled during the First Chinese Arctic Research Expedition (CHINARE-1) show great differences from one element to another. Na, K,Ca, Mg, A1, F, and Cl are the major components in the aerosols, whose contents are larger than 30 ng/m^3. The chemical elements whose contents vary between 0.1 - 30 ng/m^3 are Br,Sr, Cr, Ni, and Zn. The chemical elements whose contents are close to or slightly higher than 0.1 ng/m^3 are Rb, Ba, Zr, Th, and Pb. The contents of As, Sb, W, Mo, Au, La, Ce, Nd,Sin, Eu, Tb, Yb, Lu, Sc, Co, Hf, Ta, and Cd are less than 0.1 ng/m^3. The mass concentration data for the same element, as observed during CHINARE-1, are almost accordant, but much lower than what is observed in the China‘ s seas or the coasts of China. The enrichment factor and electron microscopic analyses and lead isotope tracing were used to distinguish their sources.Four groups of sources can be classified as follows: anthropogenic: As, Sb, W, F, Mo, Au,Cu, Pb, Cd, V; crustal: La, Ce, Nd, Sm, Eu, Tb, Yb, Lu, Fe, Sc, Cr, Co, Ba, Zr, Hf,Ta, Cs, Mn, Th, U; oceanic:Na, K, Ca, and Mg; and mixing: Rb, Sr, Ca, and Mg.     

NEW TRACE ELEMENT AND REE DATA IN THIRTEEN GSF REFERENCE SAMPLES BY ICP-MS

Analytical data on 34 geochemically significant trace elements (Sc, V, Cr, Co, Ni, Cu, Zn, Ga, Rb, Sr, Y, Zr, Nb, Cs, Ba, Hf, Ta, Pb, The, U and REE) by using Inductively Coupled Plasma Mass Spectrometry (ICP-MS), for 13 reference rock samples obtained from the Geological Survey of Finland are presented. For many elements, especially most of the heavy-REE, concentrations are reported here for the first time.     

Trace Element Geochemistry of the Permian／Triassic Boundary Section in the Selong—Xishan Area,Nyalam County,Southern Tibet,China

Samples were collected f5rom the Selong-Xishan Permian/Triassic boundary strata,Nyalam County in southern Tibet and systematically analyzed for their rare-earth elements(REE) and trace elements such as U,Th,Sr,Ba,Sc,Ta,Hf,Rb,Cs,Co,Ni,Cr,As and others with emphasis put on the distribution patterns of rare-earth elements and the variation of trace element contents along the Permial/Triassic boundary section.On this basis a discussion will be made of the paleo-ocean depositional environment.     

黄河和长江沉积角闪石亲石元素地球化学特征对比与物源辨识

为辨识黄河和长江入海沉积物中角闪石的物源差异,对采自黄河口段、长江口段以及废黄河口和苏北沿岸,共26个样点、38组粒度粗细不同的碎屑角闪石进行了矿物元素地球化学测试,获得了这些角闪石群体的50种常量和微量元素含量值.结果表明:不同粒级测量的同源角闪石元素含量除少数大离子活泼元素相对偏差较大之外,大部分元素含量差异性较小...