离子交换分离过程中铅同位素分馏评估及针对MC-ICPMS铅同位素测定的分离纯化方法的修正

本文对分离纯化样品过程中铅同位素的分馏进行了评估,并描述了适于MC-ICPMS同位素测定的分离纯化方法。利用AG1-X8阴离子交换树脂分离纯化样品中铅的过程确实导致了铅同位素的质量分馏。尽管分离纯化过程导致的铅同位素分馏程度较小(0.43‰amu-1),但明显超出了仪器的测试误差(0.23‰amu-1),如果样品中铅的回收率太低,会导致铅同位素测试值明显偏离真值。利用AG1-X8阴离子交换树脂,以0.2mL 1mol/L HBr溶液为上样介质,以5mL 1mol/L HBr和0.5mL 2mol/L HCl溶液为淋洗液,1.5mL 6mol/L HCl溶液为洗脱液,利用该分离流程可以保证获得样品中铅同位素的准确值。在本实验研究条件下,相对于过柱前样品,前期淋洗液富集铅的轻同位素(δ208Pb0),后期淋洗液富集铅的重同位素(δ208 Pb0),表明在该实验条件下,铅的重同位素组分比轻同位素更容易和树脂结合,AG1-X8阴离子交换树脂吸附铅的配分系数208 D/204 D大于1。解吸被树脂吸附铅的过程中,铅在不同络合形式间的交换反应可能导致了铅同位素的分馏效应,意味着无机络合物或者有机大分子参与反应的过程可能会导致铅同位素的分馏。     

T-检验在杭州市不同环境介质中铅同位素组成及其来源判别中的应用

应用Microsoft Excel软件中"数据分析"工具之T-检验,对杭州地区不同环境介质的铅同位素组成(206Pb/207Pb比值)进行了均值相等假设检验。通过T-检验,揭示了杭州市哪些环境介质具有相似或不同的铅同位素组成。结果表明,汽车尾气铅具有独特的铅同位素组成而不同于其它环境介质;汽车尾气铅对环境的污染导致环境中铅同位素组成逐渐偏离原值,如城区表土污染最为严重,其206Pb/207Pb比值已与土壤的残渣显示有显著差异,西湖表层沉积淤泥也与深部沉积柱样品有明显的不同。大气和水与多个环境介质具有相似的铅同位素比值,说明大气与水在环境中能与多种环境介质进行同位素物质交换,对污染的扩散起了重要的作用;茶叶与大气有相似的铅同位素比值,说明大气(降尘)对茶叶铅有较大的贡献。而运河沉积物与城区表土铅同位素比值高度一致则说明运河沉积物可能就是来自城区流失的表土。通过实例,介绍了Excel中T-检验在地球化学研究中的应用。     

杭州西湖与运河沉积物铅同位素组成及其示踪意义

西湖底部表层沉积淤泥与沉积柱中沉积物的铅同位素组成存在明显的差异。沉积柱中206Pb/207Pb=1.1906±0.0029(2σ),208Pb/206Pb=2.0858±0.0074(2σ),而表层沉积淤泥的206Pb/207Pb=1.1705～1.1726,208Pb/206Pb=2.1052～2.1069,存在明显的异常。沉积柱中铅同位素组成演变特征表明,西湖沉积柱的上部受到了现代人为的铅污染,污染物厚度35cm左右,其中顶部10cm污染较为严重。与杭州市有关环境样品的铅同位素背景对比表明,西湖的铅污染主要来源于汽车尾气排放铅。运河(杭州段)0～30cm的沉积柱中除个别样品外,206Pb/207Pb=1.1543～1.1705,208Pb/206Pb=2.1011～2.1540,与西湖沉积柱下部沉积物中的铅同位素组成明显不同,而与西湖表层沉积淤泥的铅同位素组成一致,这表明运河沉积物存在显著的铅污染。对比表明,运河铅污染也主要来自汽车尾气,同时煤铅可能也有一定的贡献。根据西湖沉积柱中铅污染的深度与平均沉积速率估计,杭州地区的铅污染开始于1910年代,但到1970年代铅污染明显加剧。     

长春市城市土壤铅同位素组成特征及其来源解析

为查明长春市土壤铅的污染来源,采集了长春市表层(0～20 cm)土壤及城市环境污染端元(燃煤尘、汽车尾气尘,建筑尘)样品,采用X荧光光谱法(XRF)测定土壤Pb含量,用质谱仪测定各样品的铅同位素组成.分析结果表明,长春市表层土壤Pb平均质量分数44.72×10-6,是长春市土壤背景值(19.06×10-6)的2.35倍,已受到一定程度铅污染;长春市土壤铅同位素208Pb/207Pb和206Pb/207Pb比值变化较大,分别为2.249～2.473和1.158～1.213;各污染端元物质铅同位素组成差异较大,能很好区别各端元物质.运用铅同位素示踪技术追踪土壤铅的污染来源结果表明,长春市中心城区土壤铅污染主要来源于以热电二厂为代表的工业燃煤排放和历史汽车尾气残留,而与当前汽车尾气排放关系不大;建筑尘也一定程度上对城市土壤产生了影响.     

湘江长潭株段河床沉积物重金属污染源的铅同位素地球化学示踪

本次工作利用等离子质谱仪(ICP-MS)对湘江长沙-湘潭-株洲河段河床沉积物重金属含量和铅同位素组成进行了系统的分析。结果表明,河床沉积物富集V、Cr、Mn、Co、Ni、Th、U、Cu、Pb、Zn等多种重金属,其中Cu、Zn、Pb等重金属于株洲段沉积物中达高度至极度富集。沉积物重金属的富集特征暗示沉积物存在较严重的重金属污染。沉积物铅同位素组成以相对富Th铅为特征,具明显的人为源和自然源铅,其~(206)Pb/~(207)Pb值在1.1723至1.1855之间,~(206)Pb/~(208)Pb值在0.4760至0.4786之间。其中自然源铅主要为花岗岩铅,而人为源铅则为铅锌矿矿石铅和燃煤铅构成,即沉积物铅同位素组成为花岗岩铅、铅锌矿矿石铅、燃煤铅组成的三元混合铅。铅同位素比例估算显示,长沙、湘潭段沉积物铅锌矿矿石源铅比例平均依次为23%、32%,燃煤源铅比例平均依次为47%、23%,自然源铅比例平均依次为30%、45%;株洲段沉积物的自然源铅比例较低,平均为17%,而矿石铅和燃煤铅的比例较高,平均依次为34%和49%。V、Mn、Co、Cu、Zn、U等其他重金属与Pb一样,长沙、湘潭段沉积物人为源比例小于67%,株洲段沉积物人为源比例达70%。因此,湘江长潭株段河床沉积物重金属污染问题值得引起高度重视。     

用于MC-ICP-MS测定环境样品中铜、锌同位素的化学分离方法

对不同离子交换柱、淋洗体积、盐度、分离次数等一系列影响铜、锌纯化分离效果的条件进行了探讨,确定了环境样品(湖泊沉积物、植物和颗粒物)中铜、锌同位素测定时化学分离的最佳条件。采用AGMP-1(100～200目)阴离子交换树脂,以7mol/LHCl+0.001%H2O2、2mol/LHCl+0.001%H2O2、0.5mol/LHNO3作为淋洗液,分别在适当的体积接收淋洗液,可以有效地分离沉积物、植物和悬浮物等样品中的铜和锌。化学分离过程中Cu和Zn的回收率接近100%,同位素分馏在测试误差范围以内。将此方法应用于对红枫湖和阿哈湖水体悬浮物、植物和鱼类等样品中Cu、Zn的分离,经MC-ICP-MS测试后,准确获得了这些样品的Cu、Zn同位素组成。     

中印度洋脊Edmond区热液硫化物的形成——来自铅和硫同位素的约束

位于中印度洋脊23°52’S的Edmond热液区发现于2000年,属于典型的以玄武岩为宿主的活动热液区。首次测得了Edmond热液区9件硫化物的铅同位素和6件样品的硫同位素组成,结果表明:硫化物矿石的206Pb/204Pb为17.879～17.970,207Pb/204Pb为15.433～15.550,208Pb/204Pb为37.743～38.130。Pb-Pb图解表明,Edmond热液区硫化物的铅同位素数据与中印度洋脊玄武岩的铅同位素组成较一致,与印度洋沉积物和锰结壳相比具较低放射性成因铅的特征,说明硫化物中的铅主要来源于地幔(玄武岩),海水的贡献微弱。硫化物的δ34S为5.7‰～7.2‰,明显高于玄武岩的硫同位素组成(δ34S≈0‰),认为Edmond热液区硫化物中的硫除地幔的贡献外,海水中硫酸盐还原作用产生的硫的贡献可能超过30%。中印度洋脊Edmond热液区存在非常活跃的浅循环系统,可能是造成硫化物中硫同位素组成偏重的主要原因。     

黔中白云岩同化剖面的铅同位素组成及物源的指示

碳酸盐岩上覆红土的形成模式是一个争议的问题,尤其是形成该红土的物质来源争议最大.本文对贵州中部平坝剖面进行了铅同位素的综合分析,结果显示全岩样品的Pb同位素组成显示是以长石矿物为主的"普通铅",下伏三叠纪白云岩样品的n(206Pb)/n(204Pb)为19.29,风化剖面全土样品的n(206Pb)/n(204Pb)约为...     

MC-ICP-MS测定积累植物中Cu、Zn同位素的化学分离方法研究

多接收器等离子体质谱仪(MC-ICP-MS)高精度同位素组成的准确测定,依赖于对样品中待测元素的分离纯化.本研究比较了两种溶样方法对有机样品积累植物海州香薷的消解效果,检测了AG MP-1阴离子交换树脂对样品中Cu、Zn的分离效果,并测定了样品中的Cu、Zn同位素组成.结果表明:①两种不同溶样方法均能有效地破坏累植物海州香薷样品中的有机质;②AG MP-1树脂能有效分离纯化植物中的Cu、Zn,经过AG MP-1树脂一次交换分离和二次交换分离的植物根样品的Cu接收液基体元素的去除基本没有差别,经过一次交换分离的Zn溶液,基体元素也基本除去,可以用于MC-ICP-MS对Cu、Zn同位素组成高精度的测定;③Cu、Zn同位素组成测定误差不大于仪器的长期重现性,表明样品的化学处理过程、各离子交换树脂柱分离交换过程和仪器测试过程均有很好的重现性,符合样品测定的要求.     

西藏雄村矿区Ⅱ号矿体硫、铅同位素地球化学特征

雄村矿区位于西藏冈底斯斑岩铜矿带西段,目前在该矿区发现了Ⅰ、Ⅱ、Ⅲ号斑岩型铜金矿体。文章通过Ⅱ号矿体硫、铅同位素研究,获得Ⅱ号矿体金属硫化物的δ~(34)S值为-1.6‰~-0.6‰,平均值-1.30‰,总硫同位素值(δ~(34)S_(ΣS))为0.99‰,与含矿斑岩的硫同位素组成(-2.1‰~+1‰,平均0.06‰)一致,均落入幔源硫范围,表明硫主要来自岩浆。含矿斑岩和金属硫化物的铅同位素组成~(206)Pb/~(204)Pb、~(207)Pb/~(204)Pb、~(208)Pb/~(204)Pb分别为18.460~18.560、15.586~15.622、38.603~38.727和17.972~18.425、15.528~15.593、38.024~38.489,两者的铅同位素组成基本一致,变化范围小,表明两者具有相同的来源。所有样品的铅同位素μ值为9.34~9.49,显示幔源特征,综合源区判别图解认为铅主要来源于幔源,有少量俯冲沉积物加入,矿床形成于与洋壳俯冲消减作用有关的岛弧构造环境。     

Lead Isotopic Composition and Lead Source in the Bainiuchang Ag-polymetailic Deposit,Yunnan Province,China

The Bainiuchang deposit in Yunnan Province,China,is located geographically between the Gejiu ore field and the Dulong ore field.In addition to the>7000 t Ag reserves,the deposit also boasts of large-scale Pb,Zn and Sn reserves with a lot of dispersed elements(In,Cd,Ge,Ga,etc.).We have determined systematically the Pb isotope composition of the deposit.The Pb isotope ratios of the ores that are of sea-floor exhalative sedimentary origin in the northwest of the mining district,are ~(206)Pb/~(204)Pb=17.758-18.537,~(207)pb/~(204)pb=15.175-15.862 and ~(208)pb/~(204)pb=37.289-39.424,while those of ores that are of magmatic hydrothermal superimposition origin in the southeast of the mining district, are ~(206)Pb/~(204)Pb=17.264-18.359,~(207)Pb/~(204)Pb=14.843-15.683 and ~(208)Pb/~(204)Pb=36.481-38.838, respectively.In terms of the Pb isotope composition of feldspar in magmatic rocks or magmatic whole- rock samples from the mining district,we have determined the Pb isotope composition and acquired the Pb isotope ratios as:~(206)Pb/~(204)Pb=18.224-18.700,~(207)Tpb/~(204)Pb=15.595-15.797 and ~(208)Pb/~(204)Pb= 38.193-39.608.Then,in the light of the Pb isotope composition of metamorphic rock samples from the Proterozoic basement exposed in the Dulong ore field,we have determined the Pb isotope composition and obtained the isotope ratios as:~(206)Pb/~(204)Pb=18.434-19.119,~(207)Pb/~(204)Pb=15.644-15.693,and ~(208)Pb/~(204)Pb=38.514-38.832.And the Pb isotope ratios of Cambrian sedimentary rocks,which are exposed in the Bainiuchang mining district,are ~(206)Pb/~(204)Pb=18.307-19.206,~(207)Pb/~(204)Pb= 15.622-15.809,and ~(206)Pb/~(204)Pb=38.436-39.932.By comparing the two types of ores with respect to their Pb isotope compositions,it is indicated that lead in the Bainiuchang deposit was derived largely from the lower-crust granulite which is earlier than Neoproterozoic in age,but the Yanshanian magmatic hydrothermal fluids probably provided a part of ore-forming elements such as Sn for the ore blocks in the south of the mining district.     

Lead Isotopic Composition and Lead Source in the Bainiuchang Ag-polymetallic Deposit, Yunnan Province, China

The Bainiuchang deposit in Yunnan Province, China, is located geographically between the Gejiu ore field and the Dulong ore field. In addition to the 〉7000 t Ag reserves, the deposit also boasts of large-scale Pb, Zn and Sn reserves with a lot of dispersed elements （In, Cd, Ge, Ga, etc.）. We have determined systematically the Pb isotope composition of the deposit. The Pb isotope ratios of the ores that are of sea-floor exhalative sedimentary origin in the northwest of the mining district, are 206pb/204pb = 17.758-18.537, 207pb/204pb = 15.175-15.862 and 206pb/204pb = 37.289-39.424, while those of ores that are of magmatic hydrothermal superimposition origin in the southeast of the mining district, are 206pb/204pb = 17.264-18.359, 207pb/204pb = 14.843-15.683 and 208pb/204pb = 36.481-38.838, respectively. In terms of the Pb isotope composition of feldspar in magmatic rocks or magmatic whole- rock samples from the mining district, we have determined the Pb isotope composition and acquired the Pb isotope ratios as： 206pb/204pb -- 18.224-18.700, 207pb/204pb -- 15.595-15.797 and 208pb/204pb -- 38.193-39.608. Then, in the light of the Pb isotope composition of metamorphic rock samples from the Proterozoic basement exposed in the Dulong ore field, we have determined the Pb isotope composition and obtained the isotope ratios as： 206pb/204pb -- 18.434-19.119, 207pb/204pb -- 15.644-15.693, and 208pb/204pb = 38.514-38.832. And the Pb isotope ratios of Cambrian sedimentary rocks, which are exposed in the Bainiuchang mining district, are 206pb/204pb = 18.307-19.206, 207pb/204pb = 15.622-15.809, and 208pb/204pb = 38.436-39.932. By comparing the two types of ores with respect to their Pb isotope compositions, it is indicated that lead in the Bainiuchang deposit was derived largely from the lower-crust granulite which is earlier than Neoproterozoic in age, but the Yanshanian magmatic hydrothermal fluids probably provided a part of ore-forming elements such as Sn for the ore blocks in the south of the mining district.     

Accurate Isotopic and Concentration Analyses of Small Amounts of Pb Using Isotope Dilution Coupled with the Double Spike Technique

A new method has been developed for the simultaneous determination of Pb abundance and Pb isotopic composition with high precision and accuracy for small test portion masses by thermal ionisation mass spectrometry. In this method, a ²⁰⁵pb-²⁰⁴pb double spike is added to samples prior to the chemical separation of Pb, and the isotopic composition of the spike-sample mixture is determined rigorously by the double spike technique using a ²⁰⁷Pb-²⁰⁴Pb spike. The isotopic composition and concentration of Pb in the sample are then obtained by utilising the principle of isotope dilution. Using this technique, replicate determinations of Pb from NIST SRM 981 and GSJ JP-1 (peridotite; 0.07 μg g⁻¹ Pb) were performed. The measured concentration and isotopic data were identical, within uncertainty, to published data or to data that were determined independently in this study. The application of this method to U-Pb dating and the determination of the "initial" Pb isotopic composition was also tested. Lead isotopic compositions and the concentrations of Pb, Th and U were determined for a single batch of samples, through the addition of ²⁰⁵pb-²⁰⁴pb, ²³⁰Th and ²³⁵U spikes to samples prior to chemical separation. Also in these experiments, we confirmed that this routine gives accurate data for Pb, Th and U concentrations and Pb isotopic compositions.     

Lead isotope geochemical characteristics of Pb-Zn-Cu deposits on the southwestern margin of Tarim, and their significance

The polymetallic(Pb,Zn,Cu,etc) ore belt on the southwestern margin of Tarim is one of the major regions with the greatest prospecting potential in Xinjiang.Reported in this paper are the lead isotope data for 66 sulfide samples(including 50 galena samples,15 chalcopyrite samples and 1 pyrite sample) collected from such representative deposits as Tamu,Tiekelike,Kalangu,Abalieke,etc.in this ore belt.The Pb isotopic ratios of 206 Pb/204 Pb,207 Pb/204 Pb and 208 Pb/204 Pb in the galena samples range from 17.931 to 18.176,15.609 to 15.818 and 38.197 to 38.944,with the average values of 18.017,15.684 and 38.462,respectively.Those in the chalcopyrite samples range from 17.926 to 18.144,15.598 to 15.628 and 38.171 to 38.583,with the average values of 18.020,15.606 and 38.262,respectively.The pyrite sample has the Pb isotopic ratios of 206 Pb/204 Pb,207 Pb/204 Pb and 208 Pb/204 Pb to be 17.980,15.604 and 38.145,respectively.In combination with the previous Pb isotope data for sulfides,it is found that there is only a slight variation in the Pb isotopic composition of galena,chalcopyrite,sphalerite and pyrite in the ore belt.However,there is some difference in Pb isotopic characteristics between galena and chalcopyrite,especially the Pb isotopic composition of galena shows an obvious linear correlation with some other relevant parameters(e.g.β and γ).The comprehensive analysis suggested that lead in galena(maybe including sphalerite and pyrite) was derived principally from wall rocks and underlying basement,and that in chalcopyrite only originated from the basement.The single-stage model ages of these sulfides couldn’t indicate the time limit of metallogenesis(Pb,Zn,Cu,etc.),and the positive linear correlations for the Pb isotopic composition of galena are of no single-stage and two-stage Pb-Pb isochron significance.Furthermore,there are significant differences in Pb isotopic composition characteristics between the genetic type of deposits in this polymetallic ore belt and the Mississippi Valley type(MVT).In addition,the authors also pointed out that there is a phenomenon of differentiation(not paragenesis) for lead and copper elements during the process of metallogenesis in this ore belt.     

Lead isotopes as tracers of anthropogenic pollution in urban topsoils of Mexico City

A survey was performed to trace the main source of anthropogenic Pb pollution in Mexico City through Pb isotopic signatures (²⁰⁸Pb/²⁰⁴Pb, ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁶Pb/²⁰⁷Pb, and ²⁰⁸Pb/²⁰⁷Pb) from 103 urban topsoil (0–5 cm) samples. Those were collected in the metropolitan area of Mexico City and compared with isotopic compositions of leaded gasoline (LG), domestic Pb ores (DLO) and parent rock (PR). The isotope ratios (IRs) of Pb were determined by inductively coupled plasma quadrupole mass spectrometry (ICP-QMS) and total Pb concentration analyzed by wavelength dispersive X-ray fluorescence (WDXRF). The range of Pb concentrations levels in urban topsoil samples was 15–473 mg/kg. The IR values obtained for these samples were 37.965–39.718 (²⁰⁸Pb/²⁰⁴Pb), 18.375–19.204 (²⁰⁶Pb/²⁰⁴Pb), 1.177–1.218 (²⁰⁶Pb/²⁰⁷Pb) and 2.443–2.496 (²⁰⁸Pb/²⁰⁷Pb). Analyzed topsoil samples with low Pb content (<50 mg/kg) displayed high dispersion in ²⁰⁸Pb/²⁰⁴Pb values, which are determined by different natural sources. Samples with 51–200 mg/kg Pb content, shown low dispersion that revealed the mixing between the natural Pb and anthropogenic Pb. The assessment of the IR values shown that, as Pb concentration increases, a trend toward gasoline IR data has been observed. The results obtained by this research suggest that although the use of leaded petrol had been banned in Mexico since 1997, the Pb pollution in the urban topsoils due to the historical use of Pb in petrol is still significant.     

Lead isotope data from the Sar-Cheshmeh porphyry copper deposit,Iran

Lead isotope compositions of nine sulfide concentrates from ore samples from the Sar-Cheshmeh deposit are reported. They range from virtually unaltered granodiorite through varying degrees of potassic alteration to ores showing strong phyllic alteration (sericite veins). The samples without strong phyllic alteration have fairly uniform lead isotope compositions around ²⁰⁶Pb/²⁰⁴Pb=18.6, ²⁰⁷Pb/²⁰⁴Pb=15.6, and ²⁰⁸Pb/²⁰⁴Pb=38.7. Two samples with sericite veins have markedly more radiogenic lead. It is concluded that the fluid responsible for the potassic alteration and the associated mineralization was essentially magmatic, whereas convecting meteoric water from the country rock acted as a mineralizing solution during phyllic alteration. In the context of the plumbotectonics model, the deposit has a typical orogen signature intermediate between primitive and mature island-arc settings.     

Lead isotope systematics of vein-type antimony mineralization,Rheinisches Schiefergebirge,Germany: a case history of complex reaction and remobilization processes

Mesothermal vein-type Sb mineralization in the Rheinisches Schiefergebirge, Germany, is characterized by two different mineralization styles, which are (1) extensional quartz-stibnite vein systems, and (2) (Cu)-Pb-Sb sulphosalt assemblages in overprinted pre-existing Pb-Zn veins. A detailed Pb isotope study of 52 representative samples from both mineralization types indicates distinct compositional patterns. (Cu)-Pb-Sb sulphosalts (meneghinite, boulangerite, bournonite) formed by reaction/remobilization are characterized by Pb isotope compositions (²⁰⁶Pb/²⁰⁴Pb=18.179-18.223), which are identical to the precursor galena (²⁰⁶Pb/²⁰⁴Pb=18.168-18.223). The Pb isotope composition of sulphosalt minerals in these vein systems was controlled by lead inherited from pre-existing galena. Stibnite and Pb-sulphosalts (zinkenite, semseyite, plagionite) formed in quartz-stibnite vein systems display Pb isotope ratios (²⁰⁶Pb/²⁰⁴Pb=18.250-18.354), which are more radiogenic than galenas from Variscan Pb-Zn ore veins (²⁰⁶Pb/²⁰⁴Pb=18.162-18.303). Detailed small-scale investigation of thrust zones hosting Pb-Zn ores and crosscutting quartz-ankerite fissure veins (Ramsbeck deposit) indicates that the Pb isotope compositions of recrystallized (galena) and remobilized phases (boulangerite, semseyite, bournonite) are arranged along a linear trend. This is interpreted as mixing between primary galena with ²⁰⁶Pb/²⁰⁴Pb᜞.206 and overprinting hydrothermal fluids with a more radiogenic composition (²⁰⁶Pb/²⁰⁴Pb⁾.354), expressed by intermediate compositions (²⁰⁶Pb/²⁰⁴Pb=18.256-18.334) of newly-formed sulphosalts. The Pb isotope systematics of the vein-type Sb mineralization is in accordance with a model of Pb extraction from similar crustal sources (Palaeozoic sedimentary sequences) at different times.     

冲绳海槽Jade热液活动区块状硫化物的铅同位素组成及其地质意义

新测行Ｊａｄｅ热液活动区中５件块状硫化物样品的铅同位素组成,具有较小的变化范围,表现出较均一的铅同位素组成特征。在Ｐｂ－Ｐｂ图解上,块状硫化物的铅同位素数据构成线形排列,与该区沉积物和蚀变火山岩的铅同位素组成一致,而与该区新鲜火山岩相比具较高的放射成因铅,证实了该区海底块状硫化物中的铅是由沉积物长英质火山岩来源铅共同构成的混合铅。不同热液活动区铅同位素组成对比研究表明,地质－构造环境的不同是导致各     

用双稀释法测定地质样品中的铅同位素组成

随着超净化实验室条件的完善以及多接收同位素质谱技术的成熟，铅同位素双稀释法倍受关注。用双稀释法测定铅同位素比值的方法原理，以及^204Pb—^207Pb双稀释剂的配制和标定方法。通过对标准物质NBS981和地质样品的分析测定，表明用双稀释法测定铅同位素比值，可以有效校正由质谱分析造成的同位素分馏效应，从而提高分析结果的精度和准确度。     

Lead in archaeological samples: an isotopic study by ICP-MS

Inductively coupled plasma mass spectrometry (ICP-MS) has been used to measure the concentration and isotopic composition of Pb in archaeological human and animal skeletal remains, soil from a village site of the Omaha tribe (U.S.A.) and cosmetic pigments.Lead concentrations in human bones from the Omaha tribe vary between 4.8 and 2570 μg/g, with younger people having the highest concentrations. Lead concentrations in animal bones from an Omaha village vary between 0.6 and 3.7 μg/g, and those of three soil samples range between 18 and 21 μg/g. Lead concentrations found in human bones from Anasazi (Utah, U.S.A.) and Alta (Peru) populations vary between 0.7 and 3.2 μg/g.Isotope ratios of a reagent grade Pb(NO₃)₂ solutions were measured by thermal ionization mass spectrometry (TIMS), as well as by ICP-MS to provide laboratory reference materials. The accuracy of the ICP-MS measurements relative to TIMS for the standard solution were found to be within 0.02–0.31% for²⁰⁶Pb/²⁰⁴Pb, 0.02–0.55% for²⁰⁷Pb/²⁰⁴Pb, and 0.16–0.56% for²⁰⁸Pb/²⁰⁴Pb. The precision of measurements on artifacts was 0.42–0.65% for²⁰⁶Pb/²⁰⁴Pb and 0.41–0.62% for²⁰⁷Pb/²⁰⁴Pb, whereas the precision for the same ratios for the bones was 0.85–1.8 and 0.82–1.67%, respectively. For the cosmetic lead-bearing pigments, a precision of 0.07–0.15% was found for both²⁰⁶Pb/²⁰⁴Pb and²⁰⁷Pb/²⁰⁴Pb ratios. Lead isotope ratios of artifacts give a radiogenic Pb signature, of which are close to signatures from PbZn mines of the central U.S. region. Lead isotope ratios of the pigments give non-radiogenic Pb signatures. Lead isotope ratios of the bones differ from those of the artifacts, and although similar in isotopic ratio to the pigments, they are more scattered, suggesting potential mixing of Pb from different regions.