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。     

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。     

川西甲基卡稀有金属矿田地表水中稀有金属元素分布特征及意义

2016～2018年系统采集川西甲基卡稀有金属矿田及周边地表水样品88件,测试分析了样品中Li、Be、Rb、Sr、Zr、Nb、Cs、Hf、Ta九种稀有金属元素含量及八种主要阴阳离子含量。结果表明:甲基卡矿田地表水水化学类型主要为HCO_3-Ca型。甲基卡矿区地表水中Li、Be、Nb、Rb、Cs、Ta等稀有金属元素平均含量明显高于川西河流平均值,Zr、Hf元素含量与川西河流均值相近,Sr含量远低于川西河流均值。经甲基卡矿区地表水稀有金属含量与矿脉分布空间耦合验证,地表水中Li、Rb、Cs、Be元素含量对矿脉的存在有明显的响应特征,其含量分布可以有效地服务于稀有金属矿产勘查,针对甲基卡外围地形高差大、切割深的特点,认为根据水地球化学异常来找矿也不失为一种有效方法,可以尝试运用地表水中稀有金属元素异常来缩小找矿靶区。     

湘南骑田岭岩体的稀有金属地球化学特征及其含矿性研究

骑田岭岩体位于湖南省郴州市,为一中生代复式岩体。本文运用电感耦合等离子质谱技术(ICP-MS)对穿越骑田岭岩体的大剖面上的花岗岩样品,进行了稀有金属Li、Rb、Sr、Cs、Nb、Ta、Be、Zr、Hf含量分析测试。结果表明:(1)岩体明显富集Li、Rb、Cs、Be、Zr,高于华南燕山期花岗岩平均值,Sr、Nb、Ta则相对亏损;(2)Li、Rb、Cs等稀有金属自西向东逐渐升高,Sr则逐渐降低,Nb、Ta、Hf等除了个别地方出现"特高值"之外,基本保持稳定;(3)相比于同时期的邻区香花岭岩体,骑田岭岩体虽然富集了一定量的稀有金属,但要形成或找到香花岭这样的稀有金属矿床还要注意剥蚀、保存条件。结合地球物理特征和岩体地质特征,认为骑田岭岩体自南东向北西斜向侵位的可能性很大,这可能也是造成骑田岭岩体稀有金属元素分带的原因。     

云南个旧矿区南部矿床原生晕垂直分带研究——以龙树脚矿段为例

矿床原生晕的垂直分带研究是寻找隐伏矿体和盲矿体的有效方法之一。本文通过对 30余种元素的分析 ,研究元素的分带指数、变化系数和变化指数梯度差 ,由此得出矿床原生晕由上至下的垂直分带为 :Mn Cd Zn Sn Cu Au Hg As( 1 82 0中段 ) ;Bi W Co Sb( 1 730中段 ) ;Mo Y( 1 70 0中段 ) ;Ni V Nb Sr La Sc Ti Yb Be Ag( 1 6 4 0中段 ) ;Pb Ga B Ba( 1 5 2 0中段 )。 30种元素的分带序列为 :Mn Ag1 Pb1 Cd Zn Sn Cu Au Hg As Bi W Co Sb Mo Y Ni V Nb Sr Cr La Sc Ti Yb Be Ag2 Pb2 Ga B Ba。     

中国东部岩石地球化学图

1986～1995年开展的中国东部地壳与岩石化学组成研究在中国东部(105°E以东)约330万km2的范围内系统采集了500余条标准地层剖面、800多个有代表性的火成岩体和变质杂岩体,总计28253件岩石样品,组合成2718件分析样品,对每个岩石组合样品的63种元素含量进行了准确测定,积累了大量的高质量的元素含量分析结果.选择60种元素SiO2、Al2O3、Fe2O3、FeO、MgO、CaO、Na2O、K2O、CO2、Ag、As、Au、B、Ba、Be、Bi、Cd、Cl、Co、Cr、Cs、Cu、F、Ga、Ge、Hf、Hg、Li、Mn、Mo、Nb、Ni、P、Pb、Pd、Pt、Rb、S、Sb、Sc、Se、Sn、Sr、Ta、Th、Ti、Tl、U、V、W、Zn、Zr、Y、La、Ce、Nd、Sm、Eu、Tb、Yb和Lu制作了中国东部岩石地球化学图.根据中国东部各省区区域地质志和1:50万地质图首次编制的中国东部岩石地球化学图基本反映了与特定岩石性有关的岩石地球化学元素含量分布特征、与大地构造单元有关的区域地球化学元素含量的宏观分布特征及不同大地构造单元元素含量背景的变化趋势.例如,CaO、(MgO) 、CO2和Cl的高背景反映地是碳酸盐岩地区,铁族元素Fe2O3、FeO、Mn、Ti、V、Cr、Co、Ni及MgO、Cu、Zn、P、Ga、Nb、Ta、Zr、Hf、Sc和Eu的高背景反映了基性火山岩地区,SiO2和K2O的高背景反映地是大面积分布的酸性岩石地区的地球化学特征.内蒙古兴安褶皱带为SiO2、K2O、Ag、As和Be的高背景分布区域,华北地台边缘、大别造山带和苏鲁造山带为Sr和Ba高背景分布区域,豫西台隆为Cu、Pb、W和Sc的高背景分布区域.南秦岭、西秦岭造山带以挥发性元素Hg、As、Sb、B以及Cd、Se、S的高背景显著特点.对于整个华南褶皱系而言,W、Sn、Bi、Mo、Rb、Cs、Tl、U、Th、Pb、Y和REE(Eu除外)为高背景,此外东南沿海火山岩带有是SiO2、K2O的高背景,而赣南闽西褶皱带还是碱金属Li,稀有元素Be、Nb、Ta,分散元素Cd及F的高背景.     

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.     

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.     

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.     

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...