大西洋洋中脊TAG热液区硫化物铅和硫同位素研究

位于大西洋洋中脊26.08°N的 TAG 热液区是目前己知的赋存在无沉积物覆盖的洋中脊区的一个最大的海底热液硫化物矿床。新测得来自 ODP-158航次钻孔的9件热液硫化物的铅、硫同位素组成;2件铁锰氧化物和1件底盘玄武岩的铅同位素组成。结果表明,矿石硫化物的铅同位素组成~(206)Pb/~(204)Pb 为18.2343～18.3181,~(207)pb/~(204)Ph 为15.4717～15.5061,~(208)Pb/~(204)Pb 为37.7371～37.8417;它们位于该区底盘玄武岩(~(206)Pb/~(204)Pb=18.1454,~(207)Pb/~(204)Pb=15.4572,~(208)Pb/~(204)Pb=37.6534)和近洋底铁锰氧化物(~(206)Pb/~(204)Pb,~(207)Pb/~(204)Pb,~(208)Pb/~(204)Pb 分别为18.6907～18.9264,15.5615～15.6279,38.1164～38.3687)的铅同位素组成之间。三者呈线性相关关系,说明硫化物中铅来源于地幔(玄武岩)与海水(铁锰氧化物)的两端元混合。硫化物的硫同位素组成δ~(34)S 为6.2‰～9.5‰,它明显高于地幔玄武岩的硫同位素组成(δ~(34)S=±0‰),也高于东太平洋海隆 EPR21°N(δ~(34)S=0.9‰～4.0‰)和大西洋洋中脊 MAR23°N(δ~(34)S=1.2‰～2.8‰)等热液活动区硫化物的硫同位素组成,这一特征反映了 TAG 热液体系中硫来源于地幔玄武岩硫与海水硫酸盐无机还原作用产生的硫的两端元混合。此,铅硫同位素研究为现代大洋底热液硫化物矿床形成过程中矿质来源及流体混合作用提供了十分有益的信息。     

滇西保山地块金厂河铁铜铅锌多金属矿床硫铅同位素特征与成矿物质来源示踪

滇西金厂河铁铜铅锌多金属矿床位于保山地块北部,是"三江"多金属成矿带内典型矿床之一。对该矿床开展硫铅同位素示踪研究,探讨成矿物质来源,并结合构造背景和成矿时代分析了矿床成矿机制。样品测试结果表明,矿石中硫化物的δ~(34)S值为+2.5‰～+11.1‰,平均值为+5.65‰,硫同位素来源为深部幔源岩浆和岩浆上侵混染壳源物质形成的多种硫源同位素组合;矿石矿物铅同位素组成中~(206)Pb/~(204)Pb为18.167～18.497,~(207)Pb/~(204)Pb为15.668～15.779,~(208)Pb/~(204)Pb为38.554～38.997,铅同位素总体较稳定,显示壳幔混染特征,以上地壳铅为主,可能来源有深部侵入岩浆及赋矿围岩。由矿床成矿物质来源表现出的多源、深源-浅源的特征推测,与成矿有关的中酸性岩体隐伏在区域深部。     

LA-MC-ICPMS分析古老熔体包裹体Pb同位素组成中的误差评价

目前应用LA-MC-ICPMS分析熔体包裹体Pb同位素,由于没有同时测试U和Th的信号,导致熔体包裹体Pb同位素的研究仅局限于中生代以来的样品。本文应用LA-MC-ICPMS分析了玻璃样品以及存在显著U-Th衰变影响的古老熔体包裹体的Pb同位素组成,评价了U/Pb和Th/Pb分析误差对初始Pb同位素比值校正的影响。实验中以国际玻璃标样NKT-1G为外部标样,采用"标样-样品-标样法"进行仪器漂移和质量歧视校正,结果表明,国际玻璃标样BHVO-2G、TB-1G的208Pb/206Pb和207Pb/206Pb分析精度优于0.30%(2RSD),与推荐值的偏差小于0.30%,然而232Th/206Pb和238U/206Pb分析结果显示了较大分散性(外精度约5.0%)。根据误差传递计算,样品的年龄对初始铅的误差有很大影响。对于古生代以来的样品(年龄小于540 Ma),即使测试的232Th/206Pb和238U/206Pb与真值偏差达到10%,经过U-Th衰变校正后的Pb同位素比值与真值的偏差依然小于0.80%。因此本方法可以将熔体包裹体等地质样品的Pb同位素研究由新生代样品(年龄小于65 Ma)扩展到古生代样品。     

铅同位素分析技术在土壤铅污染源解析中的应用——以陕西凤翔长青工业园为例

土壤是产地环境的基本要素,良好的产地环境是确保食品安全的基础。铅在土壤中具有难以降解、持久性污染等特点[1-2],是土壤环境中具有潜在危害的污染物之一。研究土壤铅污染来源及各污染源的相对贡献率,对治理土壤铅污染,保障食品安全具有重要意义。铅(Pb)在自然界中存在四种稳定性同位素,208Pb、207Pb、206Pb,和204Pb,丰度分别为51.28%~56.21%、17.62%~22.1%、20.84%~27.48%,和1.04%~1.65%[3]。其中,前三种是232Th(钍)、235U(铀)和238U放射性衰变的终产物,为放射成因稳定性同位素;204Pb的半衰期为1.4×1017a,远大于地球的年龄(4.6×109a),可看作是稳定性同位素。铅同位素比率主要由地质形成初期铀和钍的相对含量及此后的衰变时间所决定,在地球化学上具有显著的区域化分异特征,但在同一区域相当一致[4]。因此,铅同位素比率可作为含铅物质的一种"指纹"来识别铅的来源[5]。铅同位素组成有多种表示方法。在地球化学领域、特别是环境科学领域通常用同位素比率来表示其组成,如206Pb/207Pb、208Pb/206Pb、208Pb/204Pb等。由于204Pb在自然界中丰度较低,测定精度较差,所以一般选择206Pb、207Pb和208Pb三者中任意二者的丰度比(比率)来研究铅的来源[6-9]。近几十年来,铅同位素比率分析技术已被广泛用于考古[10-14]、地球化学[7,15]、大气污染源解析[16-19]等方面。土壤铅污染源解析是产地环境评价和食物链铅来源分析的重要内容。本研究以陕西凤翔长青工业园为目标区域,采集污染源端元样品(矿石、燃煤)、大气降尘,耕层土壤和背景土壤样品,用ICP-MS测定铅元素含量及同位素比率值(206Pb/207Pb和208Pb/206Pb),结合二元混合模型和三元混合模型计算各污染源对耕层土壤铅的贡献率,旨在分析耕层土壤铅污染的程度和铅污染的来源,解析各污染源对土壤铅污染的相对贡献率,探讨土壤铅污染源解析方法。结果表明:污染端元介质——铅锌冶炼厂矿石206Pb/207Pb、208Pb/206Pb分别为1.1137±0.0027、2.1648±0.0033;焦化厂燃煤206Pb/207Pb、208Pb/206Pb分别为1.0938±0.0066、2.1290±0.0044;热电厂燃煤206Pb/207Pb、208Pb/206Pb分别为1.1752±0.0035、2.0712±0.0111(详见表1);耕层土壤206Pb/207Pb、208Pb/206Pb分别为1.1824±0.0088、2.0771±0.0078;背景土壤206Pb/207Pb、208Pb/206Pb分别为1.2214±0.0032、2.0384±0.0017;大气降尘206Pb/207Pb、208Pb/206Pb分别为1.1353±0.0049、2.1189±0.0035(详见表2)。该区域铅锌冶炼活动对耕层土壤铅的贡献率约为18.43%,焦化厂燃煤对耕层土壤铅的贡献率约为9.36%,热电厂燃煤对耕层土壤铅的贡献率约为19.71%,背景土壤对耕层土壤的贡献率约为52.5%。该区域耕层土壤中的铅主要来源于背景土壤。本研究表明铅同位素解析技术是一种解析土壤铅污染来源的有效手段。     

金顶超大型铅锌矿床的成矿金属来源——来自铅同位素组成的制约

金顶矿床是世界著名的超大型铅锌矿床,其巨量的金属堆积引起许多学者对成矿金属来源的关注。前人通过铅同位素示踪研究,提出了成矿金属来自地幔、上地壳、下地壳及不同端员混合等不同认识。理论分析表明,这些观点认识的差异可能源于不同作者分析铅同位素数据存在测试误差。基于此,笔者在金顶矿床选择了7个代表性硫化物样品,再次进行了铅同位素分析。结果显示,矿床铅同位素组成为~(206)Pb/~(204)Pb=18.3945~18.4429、~(207)Pb/~(204)Pb=15.6412~15.6583、~(208)Pb/~(204)Pb=38.6266~38.6772,在铅同位素演化模式图解(Zartman et al.,1979)中数据点分布集中,处于"造山带"和"上地壳"演化曲线之间,未显示出明显的线性分布特点,表明金顶矿床成矿金属来源主要为壳源;区域对比表明,金顶矿床明显比白秧坪矿带铅锌矿床贫放射性成因铅,而与区域VMS型矿床铅同位素组成更为接近,这表明金顶矿床与白秧坪矿带矿床有着不同的金属物源区,其金属可能来自盆地底部晚三叠世火山岩或其内早期的VMS矿化。     

铅同位素比值法研究辽宁东大杖子战国墓地出土铜器的矿料来源

东大杖子墓地作为辽宁乃至东北亚地区等级极高的战国时期墓地,自发掘以来一直受到学术界的高度关注,前期的研究工作主要集中在墓葬以及随葬品类型学、文化性质等方面,缺乏对该墓地出土青铜器矿料来源的研究。本文采用电感耦合等离子体发射光谱仪、扫描电镜能谱仪和表面电离型固体质谱仪对该墓地出土的7件青铜样品进行了成分和铅同位素比值分析。成分测试结果显示7件样品中有4件为铅锡青铜,2件为锡青铜,1件未知,器物功用和合金性能基本相匹配;铅同位素示踪结果显示部分器物的铜料不大可能来自内蒙古林西大井、辽宁红透山以及山西中条山等铜矿; 5件铅含量大于2%的样品铅同位素比值~(206)Pb/~(204)Pb、~(207)Pb/~(204)Pb、~(208)Pb/~(204)Pb变化范围分别为17. 685～17. 941、15. 530～15. 612、38. 080～38. 404,其铅料来自辽宁青城子铅锌矿的可能性极大。本研究有助于探索辽宁东大杖子战国墓地出土铜器的矿料来源,同时为研究战国时期辽西与辽东半岛的金属资源贸易和流通以及辽东半岛资源开发历史提供了科学的证据。     

滇东南白牛厂多金属矿床铅同位素组成及铅来源新认识

白牛厂矿床位于滇东南锡多金属成矿带中部,是一个Ag、Pb、Zn、Sn等共生的多金属矿床,但成因争议较大.前人引用早期矿床矿石矿物铅同位素数据得出矿石铅主要来源于基底岩石淋滤,矿床经历了热水沉积+岩浆热液叠加两个成矿阶段的结论.本文采用最新铅同位素数据系统研究了白牛厂矿床的铅同位素组成,其中,白牛厂矿床矿石矿物的铅同位素组成206Pb/204Pb、207Pb/204Pb和208Pb/204Pb分别为17.264～18.537、14.843～15.862和38.481～39.424;薄竹山花岗岩长石铅同位素组成206Pb/204Pb、207Pb/204Pb和208Pb/204Pb分别为18.301～18.387、15.611～15.670和38.677～38.904;薄竹山岩体接触带型矿床(点)矿石矿物铅同位素组成206Pb/204Pb、207Pb/204Pb和208Pb/204Pb分别为18.302～18.417、15.603～15.692和38.596～38.868;区域地层及矿区地层钻孔样品铅同位素组成206Pb/204Pb、207Pb/204Pb和208Pb/204Pb分别为18.307～19.206、15.622～15.809和38.436～39.932.对比四者铅同位素组成特征,白牛厂矿床矿石矿物、薄竹山花岗岩长石、薄竹山岩体接触带型矿床(点)矿石矿物具有一致的铅同位素组成,与地层铅同位素组成相差甚远,表明白牛厂矿床铅主要来自岩浆作用,在侵入的过程中可能受到了地层的轻度混染.矿床地质特征及近期地球化学和年代学研究成果表明,白牛厂矿床的形成主要受岩浆作用影响,沉积成矿作用在白牛厂矿床很可能是不存在的.     

相山铀矿田铅锌矿化同位素特征及成矿物质来源探讨

相山铀矿田科学深钻中发现了多段铅、锌、铜、金等多金属矿化。笔者通过铷、锶、铅、硫同位素组成测试,获得铅锌矿石、盖层火山岩和基性岩脉的锶同位素初始比值,分别是:0.71914～0.72661、 0.71024～0.72080、 0.70880;矿石中硫化物的Pb同位素比值分别为~(206)Pb/~(204)Pb=18.076～18.262、~(207)Pb/~(204)Pb=15.597～15.725、~(208)Pb/~(204)Pb=38.476～38.89;铅锌矿化的δ34S值变化范围很窄,具有峰值集中和塔式分布的特征。矿石锶同位素的初始值0.712;在铅同位素构造演化模式图上,铅锌矿石分布在地壳演化线下方,靠近造山带演化线,认为成矿物质主要来源于上部地壳,具有明显参与强烈造山作用的特征,可能受到造山作用的叠加富集。S同位素特征显示,铅锌成矿作用可能受到岩浆热液作用的控制。     

河南省西峡县水地沟金矿地质特征及 S、Pb同位素示踪

水地沟金矿是河南省北秦岭高庄-二郎坪金多金属矿成矿带内新发现的金矿,为探讨其成矿物质来源及成矿物质释放机制,对水地沟金矿矿石进行了S、Pb同位素分析。4件黄铁矿样品的δ~(34)S值介于0. 5‰～4. 5‰,平均值为2. 5‰,具有塔式分布特征,峰值在2‰～4‰之间,显示幔源硫特征。7件样品的~(206)Pb/~(204)Pb、~(207)Pb/~(204)Pb和~(208)Pb/~(204)Pb的比值范围分别为15. 80～18. 32、15. 11～15. 68和35. 17～38. 39,它们的μ值、△α值、Δβ值和Δγ值的范围依次为8. 97～9. 85、32. 93～74. 31、-1. 98～30. 64和4. 10～50. 61。在~(206)Pb/~(204)Pb-~(207)Pb/~(204)Pb比值图解中,水地沟金矿样品点位于下地壳铅演化趋势线和上地壳铅演化趋势线之间,在~(206)Pb/~(204)Pb-~(208)Pb/~(204)Pb比值图解中,它们集中于上地幔和造山带铅演化趋势线两侧,铅同位素Δβ-Δγ图解表明它们位于地幔Pb、上地壳Pb和上地壳与地幔混合的俯冲带Pb三个源区内。S、Pb同位素特征表明水地沟金矿成矿物质来源于上地幔-下地壳,成矿过程中有上地壳物质加入。水地沟金矿床的形成与北秦岭燕山期陆内(板内)造山过程密切相关,它是区域岩石圈拆沉作用的产物。在这一区域岩石圈灾变过程中,不仅使水地沟岩石圈-软流圈系统内不同源区的流体混合,造成了"宽泛"的S、Pb同位素示踪结果,而且有利于深部流体的大规模快速释放,说明水地沟金矿及其邻区具有大的成矿潜力。     

西藏北部舍索与拉屋铜矿床硫化物铅同位素特征

本文在系统的野外地质工作基础上,对舍索与拉屋矿床的矿石硫化物铅同位素组成进行综合分析,进而示踪其成矿物质来源。结果显示,舍索矿区矿石硫化物铅的206Pb/204Pb值为18.517~18.776,207Pb/204Pb值为15.671~15.756,208Pb/204Pb值为38.955~39.33;拉屋矿区矿石硫化物铅的206Pb/204Pb值为18.651~18.757,207Pb/204Pb值为15.707~15.823,208Pb/204Pb值为39.183~39.561。研究表明,舍索与拉屋矿床矿石硫化物铅同位素含量比值具有明显的上地壳特征,指示两个矿床成矿物质主要来自上地壳。其中舍索矿床成矿物质富集受燕山期岩浆作用影响,而拉屋矿床部分成矿物质由晚石炭纪地幔物质的喷流沉积作用提供。     

Evaluation of lead isotopic methods for uranium exploration, Koongarra Area, Northern Territory, Australia

Analysis of radioactive (²¹⁰Pb) and stable lead isotopes in near-surface samples has been tested as a method of uranium exploration in the Pine Creek Geosyncline, Northern Territory, Australia. The lead isotopes were extracted from the samples by a mild leaching agent and were measured by alpha spectrometry for ²¹⁰Pb and by mass spectrometry for stable lead isotopes. The results are compared with those obtained by conventional methods utilizing measurements of radioactivity and radon (Track Etch) in situ and ²²⁶Ra, ²²⁸Ra and U contents of soils. The major problems addressed were whether the lead isotopic methods are more sensitive than the conventional methods and whether they can discriminate “real” anomalies from the common barren anomalies found in black soils and swamps which contain radium in excess of the uranium present.Four test areas, representing a range of exploration problems, were chosen in the vicinity of the Koongarra uranium deposits and 25 samples from each area were analyzed. Most samples have more ²²⁶Ra than uranium. Radium analyses of several water samples show the source of this radium to be non-uraniferous rocks within the Kombolgie sandstone. The results for soil ²²⁶Ra, radon, scintillometry and ²¹⁹Pb were generally closely correlated, and as a result, the ²¹⁰Pb method was not considered to have any advantages over the conventional methods.At the Koongarra X prospect, which has a weak surface expression, the ratio gave the strongest indication of the underlying uranium mineralization with an anomaly to background ratio of 12.5. However, this ratio is correlated with uranium content and does not offer any particular advantages over uranium analyses alone. More subtle indications of uranium mineralization were found by relating the radiogenic lead (²⁰⁶Pb) and the thorium-derived lead (²⁰⁸Pb) to the common lead content (²⁰⁴Pb). A plot of versus (horizontal axis) is linear for country rock samples, irrespective of the amount of more recently introduced ²²⁶Ra. Samples above uranium mineralization lie off this trend, along a line of near-zero slope. By the use of this plot, indications were found of the Koongarra No. 2 orebody, which is concealed by about 40 m of barren overburden; none of the other techniques detected this mineralization.     

Pb同位素剖面化探法在甘肃玛曲地区大水金矿深部找矿中的应用

攻深找盲是大水金矿矿山勘查的主要任务。根据Pb同位素示踪的有关理论和隐伏矿预测的方法,以甘肃玛曲大水金矿区为例,利用Pb同位素剖面化探法在大水金矿典型剖面70、72勘探线采集Pb同位素样品78个,进行成矿截止深度预测。取本区域的成矿V2截止值在22.4～234.36之间,70、72勘探线在3450m标高左右V2值分别为49.11、64.83,预测70～72勘探线深部及以西成矿截止深度在3000～3100m之间,还有400～500m的勘查空间,找矿潜力大,是今后矿区勘查的重点地段。     

Anomalous Lead Isotopic Composition of Galena and Age of Altered Uranium Minerals: a Case study of Chauli Deposits,Chatkal–Qurama District,Uzbekistan

The enrichment of lead isotopic composition of nonuranium minerals, in the first place galena in ²⁰⁶Pb and ²⁰⁷Pb, as compared to common lead is a remarkable feature of uranium deposits. The study of such lead isotopic composition anomalous in ²⁰⁶Pb and ²⁰⁷Pb in uranium minerals provides an opportunity for not only identification of superimposed processes resulting in transformation of uranium ores during deposit history but also calculation of age of these processes under certain model assumptions. Galena from the Chauli deposit in the Chatkal–Qurama district, Uzbekistan, a typical representative of hydrothermal uranium deposits associated with domains of Phanerozoic continental volcanism, has been examined with the highprecision (±0.02%) MC-ICP-MS method. Twenty microsamples of galena were taken from polished sections. Six of them are galena hosted in carbonate adjacent to pitchblende spherulites or filling thin veinlets (approximately 60 μm) cutting pitchblende. Isotopically anomalous lead with ²⁰⁶Pb/²⁰⁴Pb and ²⁰⁷Pb/²⁰⁴Pb values reaching 20.462 and 15.743, respectively, has been found in these six microsamples in contrast to another fourteen in which the Pb–Pb characteristics are consistent with common lead. On the basis of these data and with account for the 292 ± 2 Ma age for the Chauli deposit, the age of epigenetic transformation of uranium ores of this deposit has been estimated. During this process, radiogenic lead partly lost from pitchblende was captured into galena. The obtained date is 170 Ma. In the Chatkal–Qurama district, these epigenetic processes are apparently caused by the interaction of uranium minerals with activated underground water under tectonic activity and relief transformation, which took place from the post-Permian (i.e., after the Chauli formation) to the Jurassic period.     

铅同位素示踪在大气降尘重金属污染来源解析中的应用

为了分析大气降尘中铅的污染来源,解析各污染源对大气降尘铅的相对贡献值,在厦门市不同功能区采集了29个大气降尘样品。用热电质谱仪测定了大气降尘的总铅同位素组成,用ICP-MS测定样品酸可溶相铅同位素组成。结果表明,厦门市大气降尘铅同位素²⁰⁶Pb/²⁰⁷Pb值变化较大,为1.111 9~1.173 8;酸可溶相铅²⁰⁶Pb/²⁰⁷Pb值与福建土壤残渣相²⁰⁶Pb/²⁰⁷Pb值相差较大,表明厦门市大气降尘受人类活动来源铅的影响较大;酸可溶相铅²⁰⁶Pb/²⁰⁷Pb值明显小于总量铅²⁰⁶Pb/²⁰⁷Pb值。铅同位素示踪表明,厦门市大气降尘铅主要来源是燃煤,其次是自然来源和汽车尾气。三元混合模型分析表明,燃煤、自然来源、汽车尾气对厦门市大气降尘总量铅的贡献率分别为48.57%、20.29%、31.14%。     

LA-ICPMS与EPMA结合测定铀矿物微区原位U-Pb年龄

晶质铀矿、沥青铀矿、铀石等铀矿物的微区原位U-Pb定年对研究铀矿床有着十分重要的意义。使用激光烧蚀电感耦合等离子体质谱(LA-ICPMS)与电子探针(EPMA)相结合的方法更加准确地测定铀矿物微区原位U-Pb年龄,既解决了EPMA不能测定同位素比值,无法准确扣除普通铅等不足,又解决了目前LA-ICPMS测定的铀矿物标样极少,标样难寻的困扰,从而有利于铀矿物微区原位U-Pb定年技术的推广使用,为铀矿床研究提供更准确的定年数据。这一定年方法不但在铀矿床的年代学研究中有重要的应用,在各种地质体的铀矿物U-Pb同位素年代学研究中也有广阔的应用前景。     

大别山北缘中生代火山—侵入岩铅同位素组成特征及其地质意义

大别山北缘中生代火山－侵入岩的１４个夺铅同位素组成表现为高的非放射性成因＾２０４Ｐｂ,较低的＾２０６Ｐｂ／＾２０４Ｐｂ比值和低且相对一致的＾２０７Ｐｂ／＾２０４Ｐｂ比值,属于明显的低Ｕ／Ｐｂ体系,并暗示它们由具低μ值的源岩衍生的。     

Concentration, isotopic composition, and sources of lead in Southern Ocean air during 1999/2000, measured at the Cape Grim Baseline Air Pollution Station, Tasmania

Southern Ocean aerosols were collected at the Cape Grim Baseline Air Pollution Station from onshore air under baseline conditions between February 1999 and April 2000. Thermal ionization techniques (TIMS) and isotope dilution mass spectrometry (IDMS) were used to measure the isotopic composition and concentration of lead in the air giving concentrations as low as 0.6 ± 0.1 pg · m⁻³. Air collected under baseline conditions for 12 months (May 1999-April 2000) yielded an overall lead concentration of 11.0 ± 0.2 pg · m⁻³ and isotopic composition of ²⁰⁶Pb/²⁰⁷Pb = 1.154, ²⁰⁸Pb/²⁰⁷Pb = 2.387 and ²⁰⁶Pb/²⁰⁴Pb = 17.93. The range in isotopic ratios was consistent with the mixing of lead from major population centers in the Southern Hemisphere in the mid to high latitudes, except for the presence of highly radiogenic lead in some samples. Contributions from radiogenic lead of up to ∼0.8% were observed. Three periods with the highest percentage contribution of radiogenic lead (>0.5%) were investigated in more detail, and 4-d back-trajectories and radon concentrations were used to help identify the sources. The sources are probably associated with the mining and processing of uranium rich ores in southern Africa and possibly South Australia.     

Genesis of the South Zhuguang Uranium Ore Field,South China: Pb Isotopic Compositions and Mineralization Ages

U–Pb isotopic analyses indicate that ores from the South Zhuguang uranium ore field, south China, have high common (non‐radiogenic) Pb contents, with variable and relatively radiogenic initial Pb contents. The U–Pb isochron method was used to date these ores, with plots of ²⁰⁸Pb/²⁰⁴Pb and ²⁰⁷Pb/²⁰⁴Pb versus ²⁰⁶Pb/²⁰⁴Pb being used to identify sample suites with similar initial Pb isotopic ratios and to normalize variable initial Pb isotopic ratios. The resulting U–Pb isochrons indicate two substages of uranium mineralization at ~57 and 52 Ma, with a later hydrothermal reformation at ~49 Ma, which homogenized Pb isotopic compositions. Initial Pb isotopic systematics indicate that the ore‐forming fluid was characterized by high ²⁰⁶Pb/²⁰⁴Pb and ²⁰⁷Pb/²⁰⁴Pb ratios and low ²⁰⁸Pb/²⁰⁴Pb ratios, suggesting that the ore‐forming fluid was sourced from Cretaceous–Paleogene red‐bed basins, rather than from magma or the mantle, with consideration of mineralization ages.     

广西苗儿山铀矿田张家铀矿床成矿时代:沥青铀矿微区原位测定

张家铀矿床是苗儿山铀矿田北部的代表性铀矿床之一,对其开展详细的成矿年代学研究不仅对认识区域铀成矿规律十分重要,也对探讨华南花岗岩型热液铀矿床的成矿大地构造背景及动力学机制具有重要意义.在详细的镜下观察基础上,采用电子探针U-Th-Pb化学法、LA-ICP-MS U-Pb同位素方法对脉状沥青铀矿进行了年代学研究.20个点的U-Th-Pb化学年龄为55.3~81.1 Ma,其中19个点的加权平均年龄为71.4±1.9 Ma.根据稀土元素特征的不同,将34个点的LA-ICP-MS U-Pb同位素年龄分为2组,第一组共15个点,其中13个点的206Pb/238U加权平均年龄为69.4±4.9 Ma;第二组共19个,其中16个点的206Pb/238U加权平均年龄为94.1±3.0 Ma.电子探针U-Th-Pb化学法加权平均年龄（71.4±1.9 Ma）与LA-ICP-MS U-Pb同位素法较年轻的一组206Pb/238U加权平均年龄（69.4±4.9 Ma）一致,代表张家铀矿床的成矿时代,LA-ICP-MS U-Pb同位素法较老的一组206Pb/238U加权平均年龄（94.1±3.0 Ma）可能是沥青铀矿受后期改造和/或样品剥蚀过程杂质矿物影响而地质意义不明确.晚中生代期间,古太平洋板块向欧亚大陆俯冲可能是控制华南大规模花岗岩型铀矿床形成的动力学机制,包括张家铀矿床在内的华南花岗岩型铀矿床大规模成矿作用可能受80~50 Ma古太平洋板块对亚洲东部的斜向俯冲动力体制的控制.