锆石微量元素及其揭示的深部过程

近十年来对锆石研究已从早期的U-Pb放射性同位素定年和锆石同位素分析,发展到大量研究锆石的微量元素。锆石微量元素不仅可以作为锆石Ti温度计估算岩浆温度,也可以用来识别锆石及其母岩的岩石类型和成因,区分岩浆熔体或者流体控制的岩浆作用、变质作用、成矿作用等深部作用过程。文中在归纳总结岩浆锆石、变质锆石、热液锆石、碎屑锆石等不同类型锆石的微量元素成分基础上,以青藏高原碰撞后超钾质岩石中产出的锆石为例,系统介绍了超钾质岩石中各类锆石的结构、年龄和微量元素特征,并应用于解释超钾质岩石成因、岩浆源区成分、岩浆演化和上部地壳物质的混染、下地壳加厚和高原隆升之间的关系。     

Spectrochemical determination of trace elements in the U.S.G.S. silicate rock standards

Spectrographic determinations for twenty trace elements in the six new U.S.G.S. silicate rock standards along with the rock standards G-1, W-1, SR-1, GR and BR are given. Most of the results represent the average of triplicate determinations on each of five splits of the portions of the standards available to the authors. Thus, the preferred values represent, in most cases, the average of fifteen replicate determinations.     

Rock Maker: an MS Excel? spreadsheet for the calculation of rock compositions from proportional whole rock analyses, mineral compositions, and modal abundance

Rock Maker is a simple software tool that computes bulk rock compositions resulting from mixing or unmixing of rocks or minerals. The calculations describe the chemical expression of processes such as magma mixing, fractional crystallization, assimilation, residual melt extraction, or formation of solid solutions. Rock Maker can also be used for the elimination of thermodynamically inactive or unwanted chemical components from the whole rock composition, such as cores of porphyroblasts that are considered not to be in equilibrium with the matrix. The calculation of the resulting rock composition is essentially based on modal proportions and compositions of different components in rocks, which may include specific portions of the rock or individual mineral phases. Compositional data, obtained using XRF, ICPMS, EDS, or EPMA, may include major and trace element concentrations. Depending upon the nature of the problem to be solved, the concentrations of oxidic and elemental components can be added to, or subtracted from, each other, producing the calculated normalized whole rock composition after completion of the investigated process (mixing, unmixing, depletion, enrichment, etc.). Furthermore, the software allows the calculation of whole rock compositions from ideal mineral compositions, for which modal proportions can be chosen from pre-defined mineral compositions. The data set includes the most common rock forming minerals and allows the addition of further phases. This section can be used to calculate the approximate whole rock compositions from petrographic modal analysis. This part of Rock Maker is specifically suitable as a teaching tool that illustrates the interrelationship between mineral compositions, modes, and the corresponding whole rock compositions.     

BAM‐S005 Type A and B: New Silicate Reference Glasses for Microanalysis

To test whether the silicate reference glasses BAM‐S005‐A and BAM‐S005‐B from BAM (The Federal Institute for Materials Research and Testing, Germany) are suitable materials for microanalysis, we investigated the homogeneity of these reference glasses using the microanalytical techniques EPMA, LA‐ICP‐MS and SIMS. Our study indicated that all major and most trace elements are homogeneously distributed at micrometre sampling scale in both types of glass. However, some trace elements (e.g., Cs, Cl, Cr, Mo and Ni) seem to be inhomogeneously distributed. We also determined the composition of BAM‐S005‐A and BAM‐S005‐B. The EPMA data of major elements confirmed the information values specified by the certificate. With the exception of Sr, Ba, Ce and Pb, our trace element data by LA‐ICP‐MS were also in agreement with the certified values within the stated uncertainty limits. The reasons for the discrepancy in these four elements are still unclear. In addition, we report new data for twenty‐two further trace elements, for which the concentrations were not certified. Based on our investigation, we suggest that both of these materials are suitable for many microanalytical applications.     

Crystallization processes beneath the southern Mid-Atlantic Ridge (40–55°S), evidence for high-pressure initiation of crystallization

New major and trace element data are reported for a suite of basalts dredge sampled from the southern MAR (40.6-52.5°S) during cruise 9309 of the R/V Maurice Ewing and cruise 32 of the S.A. Agulhas (51-54.5°S). Samples range from aphyric to moderately porphyritic with plagioclase and olivine the dominant phenocryst and microphenocryst phases. Clinopyroxene occurs rarely as a phenocryst phase. Bulk rock and quench glass samples have major element compositions ranging from moderately primitive (Mg#=68.5) to evolved (Mg#=41.1), with a comparable range in incompatible (Zr=54-232 ppm; Nb=0.8-21 ppm) and highly compatible trace element (Ni=51-289 ppm; Cr=39-949 ppm) abundances. Incompatible trace element ratios (e.g., Zr/Nb=5.9-69; Y/Nb=0.88-29; (La/Sm)_N=0.48-2.9) indicate both enriched and depleted MORB occurring along this section of the MAR, agreeing with along-ridge radiogenic isotope ratio variations delineating compositional influences of the off-axis Discovery, and a so-called LOMU-component, and ridge-centered Shona mantle plumes (Douglass et al. 1999; Douglass and Schilling 2000). Major- and trace-element variations, particularly decreasing CaO/Al₂O₃ ratios and relatively constant Sc abundances with decreasing Mg# suggest crystallization of olivine, plagioclase, and clinopyroxene in most of these basalts prior to eruption. Liquid-lines-of-descent, derived from forward modeling of various reasonable parental magma compositions at pressures between 1 atm-8 kbar, confirm clinopyroxene as an early crystallizing phase, along with olivine and plagioclase, and its pivotal role in the compositional evolution of these basalts. Pressures deduced using algorithms of Grove et al. 1992 and Michael and Cornell 1998 indicate crystallization beneath ridge segments unaffected by mantle plumes occurred predominately at depths of 3-6 kbar (10-20 km). Crystallization beneath ridge segments affected by the Discovery and Shona mantle plumes occurred over a larger pressure range (1 atm-~7 kbar), but predominantly at crustal depths (1 atm-3 kbar), possibly due to more constant magma fluxes and higher temperatures in the crust and lithosphere in these regions favoring the existence and longevity of subaxial magma chambers.     

The selenium content of U.S.G.S. standard rocks

Selenium was determined in duplicate portions from three bottles of six U.S.G.S. standard rocks by a spect rofluorimetric procedure. The following averages, as p.p.m. Se, were obtained: PCC-1, 0.031; GSP-1, 0.088; BCR-1, 0.12; SCo-1, 0.91; MAG-1, 1.3; and SGR-1, 3.7. One-way analysis of variance of the several sets of data showed no significant differences in the selenium content among bottles of any specific rock; these samples may be accepted as homogeneous for their selenium contents by this analytical method.     

Major and Trace Element Analysis of Silicate Rocks by XRF and Laser Ablation ICP-MS Using Lithium Borate Fused Glasses: Matrix Effects, Instrument Response and Results for International Reference Materials

Major and trace element compositions of fifteen silicate rock reference materials have been determined by a combined XRF and laser ablation ICP‐MS (LA‐ICP‐MS) technique on glasses prepared by fusing the sample with a lithium borate flux (sample:flux = 1:3). Advantages of this technique include the ability to measure major and trace element abundances on a single sample using a quick and simple preparation that attacks resistant phases such as zircon without the need for acid dissolution. The method is suitable for a wide variety of bulk compositions including mafic, intermediate and silicic rocks. Abundance‐normalized mass response patterns (the ratio of signal intensity to element concentration) of the LA‐ICP‐MS analyses vary systematically with major element composition, demonstrating the presence of a matrix effect that cannot be compensated by normalisation to a single internal standard element. Increasing the sampling distance between the ICP‐MS cone and the torch reduces the magnitude of this effect, suggesting that a mechanism related to residence time of ablated particles in the plasma may be at least partially responsible for the observed variations in mass response patterns. When using a matrix‐matched calibration, agreement of the LA‐ICP‐MS results with published reference values or those obtained by solution ICP‐MS is 10% relative. Analytical precision based on replicate analyses is typically 5% RSD. Procedural detection limits that include contributions from gas background and flux are 0.01‐0.1 μg g‐¹ for the heavy mass trace elements (Rb‐U). Major element analyses by XRF show excellent agreement with results obtained using a conventional heavy element absorbing flux. High quality major and trace element data for silicate rocks can be achieved by a combined XRF and LA‐ICP‐MS analysis of Li₂B₄O₇/LiBO₂ fused glasses provided an appropriate matrix‐matched calibration is adopted.     

X射线荧光光谱法测定高锶高钡的硅酸盐样品中主量元素

用百分总和检查硅酸盐岩石全分析数据的质量是分析工作者的传统做法,但对于微量元素含量较高的样品,采用X射线荧光光谱法(XRF)进行测定,如果不考虑微量元素的含量及其对主量元素基体效应的影响,往往会使主量元素含量更加偏离真实值。本文针对Sr、Ba含量较高的硅酸盐样品,通过人工配制标准样品,扩大了Sr、Ba校准曲线的定量范围,主量元素校准中加入Sr、Ba的基体校正系数,达到了主量元素定量更加准确可靠的实际效果。采用此方法分析国家标准物质,各主量元素的精密度(RSD)均小于2%;分析不参加回归的标准物质和人工配制的标准样品,主量元素的测量值与标准值(或参考值)基本一致。该方法可以满足硅酸盐的测定要求,主量元素各项结果的加和能够达到《地质矿产实验室测试质量管理规范》的一级标准(99.3%～100.7%)。     

Variability in the inorganic element content of U.S. coals including results of cluster analysis

Patterns of variability in trace element and major inorganic element content of 335 U.S. coal samples were investigated using the multivariate statistical techniques of principal component analysis and cluster analysis. Whole-coal basis values contain different information from ash basis values; therefore data expressed on each basis were treated separately. For each basis, major elements grouped together according to their occurrence in dominant inorganic groups in coal (aluminosilicates, sulfides, and elements organically bound or in carbonates), and relationships of trace elements to these groups were shown. Cluster analysis grouped samples based on their inorganic content. For data expressed on an ash basis, either three or four clusters were indicated. The three-cluster partition was similar to a partition into Eastern, Interior, and other (western) provinces. The partition into four clusters was more complex; is showed that samples from the Eastern and Interior provinces taken as a group can be divided into three clusters. One, characterized by low aluminosilicate and sulfur levels, contains both Interior and Eastern province samples. Thus not all Interior province samples are characterized by high levels of iron sulfide and associated elements; some are more similar to many Eastern province samples than to other Interior province samples.     

兰坪中新生代盆地沉积岩源区构造背景和物源属性研究--砂岩地球化学证据

沉积盆地中砂岩的地球化学成分主要受物源区控制。因此，通过分析砂岩的化学成分可以揭示盆地沉积岩的源区构造背景和物源属性。对兰坪盆地中新生界砂岩的常量成分、稀土和微量元素进行的分析，揭示盆地沉积岩的源区构造背景属被动大陆边缘和大陆岛弧，结合岩相古地理资料认为在中生代以前，盆地东侧可能主要处于被动大陆边缘环境。而西侧则可能以大陆岛弧环境为主，这与区域地质资料相吻合。沉积物源岩的原始物质应来自上地壳，以长英质岩石为主，并有少量安山质岩石和古老沉积物的混入，故兰坪中新生代盆地属典型的大陆型盆地。从而为正确认识古特提斯洋的演化和盆山转换过程提供了强有力的地球化学证据。     

Inhomogeneity of mercury in the U.S.G.S. rock standards

Mercury inhomogeneity was found between bottles of the same standard for each of the six U.S.G.S. rock standards tested. Variations between bottles amounted to at least a factor of 2 for four of the six standards. Caution is suggested when using these standards as mercury accuracy checks and as estimators of mercury geochemical abundances or cycles.     

Geochemical signature of provenance in sand-size material in soils and stream sediments near the Tobacco Root batholith, Montana, U.S.A.

Trace-element geochemistry of sandstones are being used to determine provenance. We have conducted preliminary and limited experiments to determine to what extent daughter sands retain the geochemical signature of parent rocks. Six sets of first-order stream sediments, soils from adjacent slopes, and a variety of parent rocks were collected from southwestern Montana, U.S.A. Sampling in a low-relief area ensured that climate and residence time of soils on slopes could be eliminated as variables. Sand-size fractions of stream sediments and soils, and the corresponding parent rocks (granodiorite, quartz monzonite, granite gneiss, biotite-tonalite gneiss and amphibolite) were analyzed for most major elements and selected trace elements. Petrologic modal analysis of the parent rocks and the 0.25–0.50-mm fraction of each sand was done to monitor major mineralogic control, if any, on chemical compositions of the samples.

Our data show that the abundances of the Si and Al in sediments do not discriminate provenance. Abundances of Ca, Mg, Fe and Ti may broadly distinguish between sands derived from metamorphic and igneous source rocks, at least in the area studied. Differences in abundances of the Ba and Th, and the ratio of La/Lu between granitic, tonalitic and amphibolitic parent rocks are preserved in the daughter sediments that we studied. However, the size of the Eu anomaly in the REE patterns of different daughter sediments is not diagnostic of parent rocks. Abundances of Co and Sc distinguish between sediments derived from felsic and mafic rocks. A better provenance discrimination is obtained if the ratios La/Sc, Th/Sc, La/Co, Ba/Sc and Ba/Co are used.

Petrologic modal data show that mineral contents and chemical compositions of parent rocks are compatible with each other. The chemical composition of the sands may be roughly correlated to the petrological modal data but the abundances of some minor and trace elements of sediments cannot be inferred from modal mineralogy. This is expected because these elements may concentrate in accessory minerals and/or may weather out into aqueous or clay mineral fractions; it is also compatible with conclusions of previous studies that some of these elements do not reside in sand-size fractions of siliciclastic sediments.     

Lead isotope variability in olivine-hosted melt inclusions from Iceland

The lead isotope and trace element compositions of a suite of olivine-hosted melt inclusions in primitive lava flows from the Reykjanes Peninsula in Iceland show extreme variability. Much of this variability is present in the composition of inclusions from one hand specimen of Háleyjabunga, a depleted picrite lava shield that erupted 13 ka. ²⁰⁸Pb/²⁰⁶Pb compositions in this sample span 50-90% of the total range found in Atlantic MORB, indicating that high-amplitude compositional heterogeneity is present in the mantle source of melts that aggregated to form a single eruption. The trace element and isotopic trends in the melt inclusions are coincident with those in whole rock samples from young lava flows of the Reykjanes Peninsula, and extend the total range of variation towards more depleted compositions. The incompatible trace element and lead isotope compositions of the inclusions are strongly coupled and lie close to binary mixing trends between the extreme melt inclusion compositions. These relationships indicate that the trace element variation in the melt inclusions reflects heterogeneity in the composition of the mantle source entering the melting region under the Reykjanes Peninsula. Large positive Sr concentration anomalies are present in three of the inclusions, but do not correlate with indicators of mantle melting or source variations and are likely to arise by reaction with plagioclase during crustal storage. Fractional melting of heterogeneous mantle is predicted to generate melts with a wide range of compositions, filling a large volume in trace element-isotope space. However, the compositional variations observed in the melt inclusions lie close to binary mixing curves. These observations may be accounted for by a two-stage model of melt mixing. The first stage occurs in porous channels that transport melt in the mantle and takes place before inclusion entrapment. This mixing stage generates a bimodal distribution of melt compositions that is supplied from the channels to sub-Moho and lower crustal magma lenses. The second stage of mixing occurs in these chambers, producing the binary mixing trends recorded in the inclusion compositions. The distribution of isotopic compositions observed in the melt inclusions and whole rock samples from the Reykjanes Peninsula is therefore controlled by melt mixing. These results have important implications for the interpretation of basalt composition in terms of distinct compositional entities within the upwelling solid mantle under mid-ocean ridges and ocean islands.     

Chemical and isotopic variations along the superfast spreading East Pacific Rise from 6 to 30°S

Chemical data of 39 fresh basaltic glasses from the East Pacific Rise (EPR) between 6 and 30°S and Pb, Sr, and Nd isotopic compositions of 12 basalt glasses are presented. Major and trace element data indicate a wide compositional range, including primitive basalts (Mg#=0.67) and highly evolved FeTi-basalts (Mg#=0.34) [molMg/(Mg+Fe²⁺)]. The compositional range can be attributed to low-pressure fractional crystallization. Fractionation-corrected major element concentrations provide evidence for varying mantle melting conditions. Calculations of the melting conditions suggest melt generation in a rising upper mantle column between 20 and 10 kbar, at temperatures between 1430 and 1280°C, and total degrees of partial melting between 17 and 20% by weight. Leached and hand-picked basalt glasses display large variations in ⁸⁷Sr/⁸⁶Sr (0.70235–0.70270), ¹⁴³Nd/¹⁴⁴Nd (0.51312–0.51323), and ²⁰⁶Pb/²⁰⁴Pb (18.064–18.665), but are similar to other N-type MORB from the EPR. The isotopic ratios of basalts from 13 to 23°S show strong correlations and delineate two systematic trends. From 23 to 17°S, ⁸⁷Sr/⁸⁶Sr and Pb isotope ratios increase and ¹⁴³Nd/¹⁴⁴Nd decrease in agreement with previous results (Mahoney et al. 1989). A reverse trend is indicated by basalts from 17 to 13°S. However, K/Ti and (La/Sm)_N continuously increase from 23 to 13°S. This opposite behavior indicates a recent decoupling of isotopic and minor element ratios in the mantle between 13 and 17°S. North of 13.5°S (Garrett Fracture Zone), isotopic data show no systematic variation with ridge location and display an overall weaker covariation. The results suggest that the isotopic variations and ridge segmentation appear to be unrelated and that major ridge offsets apparently coincide with changes in mantle melting conditions (P, T, F) (F, degrees of melting). There is no evidence for a systematic relationship between calculated melting conditions and second order ridge segmentation. Our isotopic data provide further evidence for regionally confined chemical variations in the mantle at 5 to 30°S. We interpret the isotopic trends as reflecting melting of distinct smallvolume and old enriched mantle components. In contrast, variations in trace elements are attributed to young mantle differentiation processes.     

Chemical Characterisation of the USGS Reference Glasses GSA-1G, GSC-1G, GSD-1G, GSE-1G, BCR-2G, BHVO-2G and BIR-1G Using EPMA, ID-TIMS, ID-ICP-MS and LA-ICP-MS

The USGS reference glasses GSA-1G, GSC-1G, GSD-1G, GSE-1G, BCR-2G, BHVO-2G and BIR-1G were investigated by different analytical techniques. All these materials have a geological (basaltic) matrix and are therefore useful in igneous geochemistry as matrix-matched reference materials for microanalytical techniques. The new GS glasses have trace elements in groups at concentration levels of about < 0.01, 5, 50 and 500 μg g^-1. Their major element compositions have been determined by EPMA, and trace elements have been analysed by LA-ICP-MS and two isotope dilution techniques using TIMS and ICP-MS. EPMA and LA-ICP-MS analyses indicated that the USGS reference glasses are homogeneous at the μm to mm scale with respect to major (variations < 1-2%) and most trace elements (variations 1-4%). Trace element data obtained from the different analytical techniques agreed within an uncertainty of 1-5%, indicating that between method results are comparable. Therefore, the preliminary working values for the four USGS GS glasses calculated from these data have a low level of uncertainty.     

浙东早白垩世火山岩组合的地球化学及其成因研究

浙东早白垩世含中性岩的火山岩组合和双峰式火山岩组合的主量元素和微量元素特征对比研究表明，中性火山岩的地球化学特征明显受到伴生的基性和酸性火山岩的影响。它们的微量元素协变关系证实：中性火山岩是由基性岩浆和酸性岩浆混合形成的。双峰式火山岩具有与含中性岩的火山岩组合相类似的主量元素特征，但两者的微量元素特征相差较大。根据东南沿海在早白垩世时期的构造背景是由挤压向伸展拉张转变，以及各种元素具有不同的扩散速度，提出了浙东早白垩世火山岩组合的形成模式：若基性岩浆和酸性岩浆仅进行了部分微量元素的交换，没有来得及发生主量元素的交换，就在伸展拉张的构造背景下喷出地表，则形成双峰式火山岩组合；若基性岩浆与酸性岩浆在地壳深处共存的时间较长，发生一定程度的主量元素交换，则形成偏基性和偏酸性的中性岩浆，若进一步发生化学成分的交换，则可形成典型的安山质岩浆，喷出地表就形成含中性岩的火山岩组合。     

四川乌斯河铅锌矿床成矿物质来源及矿床成因:来自原位S-Pb同位素证据

乌斯河铅锌矿床位于扬子板块西南缘,是川滇黔铅锌矿集区代表性大型铅锌矿床之一,估算资源量超过370万吨,Pb+Zn平均品位~15.7%。该矿床铅锌矿体主要呈层状、似层状、透镜状产于震旦系灯影组的白云岩地层中,其围岩蚀变较弱,以白云石化和方解石化为主。矿石类型主要包括块状、条带状、角砾状、脉状和浸染状等,其中矿物组成相对简单,以闪锌矿、方铅矿、白云石和方解石为主,含少量沥青和黄铁矿。该矿床地质地球化学研究程度相对较低,其成矿物质来源不清,致使该矿床存在热水沉积成因、喷流沉积-后期热液叠加改造以及MVT型等多种成因争议,难以建立统一成矿模式。本文对乌斯河铅锌矿床不同成矿阶段的硫化物（包括黄铁矿、闪锌矿和方铅矿）,开展原位硫和铅同位素地球化学研究,以查明该矿床的成矿物质来源、还原硫的形成机制和示踪成矿过程,为认识该类矿床铅锌成矿作用提供新地球化学依据。原位S同位素分析结果显示,乌斯河铅锌矿床硫化物的还原硫存在不同硫来源,成矿早阶段硫化物δ³⁴S值较低,介于+1.3‰~+14.2‰之间,暗示可能有来自于赋矿地层圈闭古油气系统中的H₂S;主成矿阶段硫化物相对富集重硫同位素,δ³⁴S值在+11.0‰~+23.3‰之间,表明其为赋矿地层的蒸发岩的热化学还原作用的产物。此外,硫化物的LA-MC-ICPMS原位Pb同位素组成分析显示,该矿床成矿金属元素主要来源于变质基底地层,水岩反应可能使赋矿地层贡献少量的成矿物质。综合矿区地质特征和已有的地球化学研究成果,本文认为乌斯河铅锌矿床属于MVT铅锌矿床,富Pb、Zn等成矿元素的流体与富H₂S的流体混合是该矿床金属硫化物沉淀的主要机制。

     

TRACE ELEMENT ANALYSIS OF TEN U.S. GEOLOGICAL SURVEY ROCK STANDARDS BY NEUTRON ACTIVATION USING A LOW FLUX REACTOR

Ten U.S. Geological Survey rock standards have been analyzed for trace elements by instrumental neutron activation using a low flux reactor and Ge detectors. Results compare favorably with the current working values for all elements except Mo. REE values that have been determined are generally slightly lower than accepted values. Data obtained for rocks that have very low trace element concentrations (e.g., BIR-1) will aid in refining the working values for these standards.     

高温熔融研制钾长石玻璃标准物质初探

激光剥蚀多接收等离子体质谱(LA-MC-ICPMS)是进行原位微区分析微量元素和同位素的重要技术之一,标准样品与样品之间的基体匹配是解决影响该技术准确分析的基体效应和分馏效应的首选方案。长石(特别是长石微区)的Pb同位素组成是示踪岩石形成和演化历史的重要途径,而LA-MC-ICPMS技术则是进行长石Pb同位素原位微区分析的关键技术,然而目前国内外尚没有合适的长石Pb同位素分析标准。文章研究探讨了利用高温炉进行原位微区分析钾长石中Pb同位素组成所用外部标准物质合成条件,结果表明,常规的74μm(200目)碎样无法得到均一的钾长石玻璃,需要将初始钾长石粉末研磨至1300目以下;高温炉合成温度为1680℃;熔融时间为2 h;采用液氮方式淬火。制成的钾长石玻璃除表面具有轻微的不均一性外,内部的Pb同位素比值为1.90779±0.00009(208Pb/206Pb,2s),0.75899±0.00004(207Pb/206Pb,2s),20.909±0.002(206Pb/204Pb,2s),15.871±0.002(207 Pb/204 Pb,2s)和39.888±0.005(208 Pb/204 Pb,2s),相应的相对标准偏差(RSD)分别为0.007%、0.008%、0.016%、0.016%和0.021%。表明利用本研究方法合成的钾长石玻璃可作为潜在的钾长石中Pb同位素组成原位微区分析外部校准物质。     

粤西大沟谷钠长石岩型金矿床成矿物质来源研究

粤西大沟谷钠长石岩型金矿床主要产于震旦系乐昌峡群呈似层状及脉状分布的钠长石岩中，钠长石岩的岩石化学成分及微量元素组成与金矿体的基本相同。黄铁矿Ｐｂ、Ｓ同位素组成可分为两组：富放射性成因铅贫＾３４Ｓ体系；贫放射性成因铅富＾３４Ｓ体系，前者与震旦系片岩的组成相似，后者为自较老富基性岩的沉积岩。