一种新的稀有金属矿床定年技术：微区原位Sm-Nd定年

¹⁴⁷Sm-¹⁴³Nd放射性同位素体系在地球科学研究中得到了广泛的应用,经典的同位素稀释-热表面电离质谱法(ID-TIMS)一直是Sm-Nd同位素高精度测定的基准技术,但具有耗时长、成本高、样品需求量大等缺点,并且难以揭示微观尺度单矿物所蕴含的地球化学信息。近年来兴起的微区原位分析,具有简单、快速、高空间分辨率的特点,可以从微米尺度示踪岩浆和热液的起源及演化过程。本文通过同时测定Sm和Nd同位素质量分馏系数,实现¹⁴⁴Sm对¹⁴⁴Nd干扰的准确校正,获得了人造玻璃、磷灰石、榍石、独居石等几种不同基体标准样品(NIST610、Durango、MAD-2、BLR-1、117531)精确的¹⁴³Nd^/144Nd比值,与推荐值在误差范围内一致。然而,由于Sm和Nd元素性质的差异,在激光剥蚀和质谱电离过程中会产生明显的元素分馏,导致¹⁴⁷Sm/¹⁴⁴Nd很难进行精确校正,本文通过在进样系统中引入液态气溶胶,有效克服了基体效...     

沙茨基海隆(Shatsky Rise)白垩纪玄武岩的地球化学特征及其地幔柱-洋中脊相互作用过程

沙茨基海隆(Shatsky Rise)是白垩纪早期形成的西北太平洋大火成岩省,其成因和演化过程目前仍存在较大争议。本次研究对沙茨基海隆白垩纪玄武岩进行了全岩主量、微量元素、Sr-Nd-Pb同位素的分析。沙茨基海隆玄武岩主要属于拉斑玄武岩,具有较亏损的大离子亲石元素和轻稀土元素以及较富集的重稀土元素的特征,没有明显的Eu异常(δEu=0.99～1.29),与正常洋中脊玄武岩(N-MORB)的微量元素配分模式较为相似。然而该系列玄武岩却具有相对较富集的初始⁸⁷Sr/⁸⁶Sr(0.702986～0.703991)和¹⁴³Nd/¹⁴⁴Nd(0.513034～0.513194)同位素比值、较富集的²⁰⁷Pb/²⁰⁴Pb(15.439～15.508)和²⁰⁸Pb/²⁰⁴Pb(37.853～38.488)同位素比值,与富集的洋岛玄武岩(OIB)和岛弧火山岩的同位素成分较为相似,且源区混入高U/Pb比值(HIMU型)的富集地幔成...     

大别山双河超高压变质矿物Ｏ同位素平衡及其对Sm-Nd和Rb-Sr等时线年龄有效性的制约

对大别造山带双河超高压榴辉岩和片麻岩Sm-Nd和Rb-Sr等时线矿物进行了O同位素地质测温。尽管Sm-Nd等时线给出一致的三叠纪年龄(213~238 Ma)，同一样品Rb-Sr等时线却给出侏罗纪年龄(171~174 Ma)。片麻岩、榴辉岩和榴闪岩矿物对O同位素测温得到600~720℃和420~550℃两组温度，分别对应于约225±5 Ma榴辉岩相变质和约175±5 Ma角闪岩相退变质条件下停止同位素扩散交换的温度。同一样品三叠纪Sm-Nd等时线年龄的保存、侏罗纪Rb-Sr等时线年龄的出现以及有规律的O同位素温度，表明在角闪岩相退变质过程中，Sr和O在含水矿物（如黑云母和角闪石）中的扩散速率在手标本尺度上比石榴石Nd和多硅白云母Sr的扩散速率快。     

四川盆地东部地区早中三叠世蒸发岩的锶同位素特征及其地质意义

锶同位素已经成为全球海平面变化、造山运动、古气候和古环境等全球地质事件研究与对比的有效工具之一。本文以四川盆地东部地区早中三叠世蒸发岩的野外剖面和钻孔岩心为主要研究对象,测试了碳酸盐岩、硫酸盐岩和石盐岩的锶同位素组成,并建立了相应的锶同位素演化曲线。研究结果显示,碳酸盐岩的⁸⁷Sr/⁸⁶Sr值平均为0.707 895,硬石膏岩的⁸⁷Sr/⁸⁶Sr值平均为0.708 174,石盐岩的⁸⁷Sr/⁸⁶Sr值平均为0.708 177,同时碳酸盐岩的⁸⁷Sr/⁸⁶Sr值从早三叠世的0.707 413快速增加到中三叠世早期的0.708 515,而后呈现下降趋势。从总体上看,这些⁸⁷Sr/⁸⁶Sr值与全球早中三叠世同期的⁸⁷Sr/⁸⁶Sr值数据接近,说明四川盆地东部地区早中三叠世钾盐的物质来源大部分为海水,并沉积于海相沉积环境,同时由于火山...     

内蒙古东乌旗阿尔哈达铅-锌-银矿床硫和铅同位素研究

阿尔哈达铅-锌-银矿床是近年来在内蒙古东乌珠穆沁旗境内发现的一处大型铅-锌-银矿床,其产出环境和形成机理为国内外矿床学家所关注。对该矿床代表性岩（矿）石样品进行了硫和铅同位素分析,并对其变化规律和成因意义进行了讨论。研究结果表明,围岩和矿石中硫化物δ³⁴S值变化范围为1.2‰～8.6‰,具有混源硫特征。根据共生硫化物对所确定的温度表明,该矿床的形成可划分为高温和中-低温两个阶段。17件矿石硫化物样品²⁰⁶Pb/²⁰⁴Pb、²⁰⁷Pb/²⁰⁴Pb和²⁰⁸Pb/²⁰⁴Pb比值变化范围分别为18.153~18.431,15.370~15.602和37.653~38.213,其平均值分别为18.271、15.464和37.873;3件围岩硫化物样品²⁰⁶Pb/²⁰⁴Pb、²⁰⁷Pb/²⁰⁴Pb和²⁰⁸Pb/²⁰⁴Pb比值变化范围分别为18.281~18.293,15.470~15.484和37.874~37.909,平均值分别为18.288、15.477和37.893。硫和铅同位素研究结果表明,阿尔哈达铅-锌-银矿床成矿物质分别来自泥盆系火山-沉积岩和印支期花岗岩。     

第四纪黄土物源的时空差异研究现状及展望*

黄土物源研究对揭示第四纪以来东亚大气环流格局的演化和构造—气候之间的相互作用具有重要意义。目前已应用多种物源示踪方法对黄土物源开展了大量研究,但对黄土物源时空差异规律及其动力学机制尚未取得较为一致的认识。在综合分析黄土物源研究现状的基础上,重点从影响⁸⁷Sr/⁸⁶Sr值和 ¹⁴³Nd/¹⁴⁴Nd 值组成及单颗粒碎屑锆石U-Pb年龄谱构成的因素角度,分析了第四纪黄土的物源及可能变化,获得以下认识: (1)第四纪黄土沉积物的⁸⁷Sr/⁸⁶Sr值变化幅度可达0.002 580~0.004 949,远远超出实验室分析测试误差(<0.000 018)或由Sr同位素衰变带来的影响(2.6 Ma时段小于0.000 026,1个冰期旋回小于0.000 001); ¹⁴³Nd/¹⁴⁴Nd 值亦发生了较显著变化(0.000 095~0.000 240),其变化幅度远大于实验室的分析测试误差(<0.000 010)及衰变导致的 ¹⁴³Nd/¹⁴⁴Nd 值(<0.000 013)变化。因此,在黄土中检测到的Sr-Nd同位素组成的变化应具有较明确的地质意义。(2)第四纪黄土沉积物中无论全岩还是主要粒径组分的⁸⁷Sr/⁸⁶Sr值和 ¹⁴³Nd/¹⁴⁴Nd 值的变化都与气候代用指标变化不同步,难以从气候变化角度进行解释,可能更多地反映了源区的变化。(3)与Sr-Nd同位素示踪体系相比,单矿物或单颗粒的物源示踪体系对物源区变化的响应更为敏感,在追踪第四纪黄土沉积物源区时空差异方面具有较明显的优势。(4)基于碎屑锆石U-Pb年龄谱对黄土物源的有限研究揭示黄土高原的黄土在地质历史时期可能发生了原始物源区显著的时空分异,特别是不同剖面都反映出了1.2 Ma前后黄土主要源区的变化,表明通过锆石U-Pb年龄谱研究黄土物源时空差异规律具有揭示岩石圈、大气圈、水圈耦合作用过程及历史的巨大潜力。     

娘娘山碱性火山-侵入岩特征及成岩定量模拟

本文通过对铜井娘娘山旋回中生代火山-侵入岩系岩石化学、微量、稀土元素以及铷锶、钐钕等同位素详细研究,认为这套岩石具高碱、硅不饱和、强烈富集不相容元素和轻稀土特征。岩石的~(87)Sr/~(86)Sr初始比值为0.7070—0.7073,∈_(Nd)值为-3.4—3.3,利用二元混合模式计算得出蓝方石响岩和霓辉正长岩源区物质成分相当41%、42%上部陆壳和59%、58%亏损地幔组成的混合物,源区物质经6.4%、6.6%部分熔融形成初始岩浆,表明娘娘山旋回碱性火山-侵入岩系是壳幔混合物经部分熔融后所形成的产物。     

中祁连西段黑沟梁子花岗岩的锆石U-Pb同位素年龄及成因

黑沟粱子花岗岩岩体为中祁连山带两段野马南山巨量花岗岩的一部分,出露于野马山南北缘,岩性为黑云母二长花岗岩。δ值、NK／A值、A／NCK值、Eu负异常、δEu值、ACF图解、⁸⁷Sr/⁸⁶Sr比值、εS_r、¹⁴⁷Sm／¹⁴⁴Nd比值、²⁰⁷Pb/²⁰⁴Pb比值、ENd值等岩石化学和同位素特征表明黑沟粱子花岗岩属钙碱性过铝质岩系,浆来源于地壳物质的重熔,具S型花岗岩特点。通过对黑沟梁子花岗岩的颗粒级锆石U-Pb同位素测年,获得²⁰⁶Pb/²³⁸U表面年龄统计权重平均值为(444±17)Ma。w(Nb)-w(Y)和w(Rb)一w(Y+Nd)图和R₁-R₂图解上两个样点均落入同碰撞花岗岩区,结合前人研究成果可以确定该岩体形成于板块碰撞阶段。该岩体的锆石U-Pb年龄的确定和成因的探讨对于深入研究祁连造山带的构造演化提供了一条重要的地质信息。     

多接收器电感耦合等离子体质谱法测定土壤标准物质铜同位素组成

近年来,铜同位素在表生环境和生物地球化学中的应用越来越广泛,尤其是土壤的铜同位素组成可以示踪环境污染物来源及生物地球化学过程。目前,对土壤铜同位素进行研究时,主要以硅酸岩标准物质为标样来衡量土壤样品铜同位素测定的准确性和精确性。但土壤与硅酸岩中铜、基质离子及有机质的含量等存在很大差异(如:硅酸岩中的铜含量80μg/g,一些土壤中的铜含量很低,20μg/g),将硅酸岩标准物质作为标样来监测土壤样品的数据质量缺乏代表性。为了弥补这一缺陷,本文精确测定4个国家土壤标准物质(GBW07443、GBW07425、GBW07427、GBW07389)的铜同位素组成,并将其作为检验土壤样品铜同位素测定过程中的标准。实验中采用高温高压反应釜消解样品,利用AG MP-1M树脂进行纯化,全流程空白2ng,回收率≥98%,通过多接收器电感耦合等离子体质谱仪(MC-ICP-MS)采用标样-样品-标样间插法进行仪器分馏校正,δ~(65)Cu的长期测试外精度优于0.05‰(n=306, 2SD)。GBW07443、GBW07425、GBW07427和GBW07389的铜同位素组成分别为-0.04‰±0.04‰(n=9, 2SD)、-0.07‰±0.05‰(n=12, 2SD)、-0.06‰±0.04‰(n=12, 2SD)、-0.02‰±0.06‰(n=12, 2SD)。这些土壤标准物质的铜同位素组成均位于0附近,大致为自然界土壤铜同位素比值变化范围(-0.5‰～+0.5‰)的中间值,且样品容易获得,其化学和铜同位素组成均一,适合作为监控土壤铜同位素化学及质谱分析数据可靠性的标准物质。     

特提斯喜马拉雅带江孜地区古近纪地层源区分析——对造山带早期地壳加厚的制约

特提斯喜马拉雅北亚带江孜地区上古新统-下始新统甲查拉组记录了喜马拉雅碰撞造山带的早期地壳加厚和沉积历史。本文我们报道了甲查拉组详细的碎屑锆石U-Pb年龄和全岩Sm-Nd同位素数据。甲查拉组由青灰色厚层的岩屑砂岩夹泥岩组成,不整合覆盖在宗卓组之上,碎屑锆石主要的峰值介于350～80 Ma, 900～470 Ma以及1 300～950 Ma,次要的峰值介于2 800～1 500 Ma。全岩⁸⁷Sr/⁸⁶Sr介于0.707 505～0.713 174,¹⁴³Nd/¹⁴⁴Nd介于0.512 206～0.512 355,ε_Nd(0)介于-5.52～-8.43。甲查拉组物源区以再循环的日喀则弧前盆地和上三叠统郎杰学群为主,少量物质来自雅鲁藏布江缝合带。上述研究表明,甲查拉组沉积在周缘前陆盆地的背景下,且特提斯喜马拉雅北亚带在始新世期间经历了明显的地壳加厚。     

黑龙江争光金矿床方铅矿黄铁矿Rb-Sr年龄及地质意义

争光金矿床位于兴安地块东缘黑龙江省多宝山铜钼-金矿集区南东端,矿体产于早奥陶世闪长岩与下奥陶统多宝山组地层接触带及多宝山组中,为大型金矿.因缺乏精确的成矿年代学研究,其成矿时代一直存在争议.本文在争光金矿床地质背景和岩石矿物学研究的基础上,对矿区内12件矿石样品中共生矿物方铅矿和黄铁矿进行Rb-Sr同位素年代学研究.结...     

Mantle diversity beneath the Colombian Andes, Northern Volcanic Zone: Constraints from Sr and Nd isotopes

In order to provide mantle and crustal constraints during the evolution of the Colombian Andes, Sr and Nd isotopic studies were performed in xenoliths from the Mercaderes region, Northern Volcanic Zone, Colombia. Xenoliths are found in the Granatifera Tuff, a deposit of Cenozoic age, in which mantle- and crustal-derived xenoliths are present in bombs and fragments of andesites and lamprophyres compositions. Garnet-bearing xenoliths are the most abundant mantle-derived rocks, but websterites (garnet-free xenoliths) and spinel-bearing peridotites are also present in minor amounts. Amphibolites, pyroxenites, granulites, and gneisses represent the lower crustal xenolith assemblage. Isotopic signatures for the mantle xenoliths, together with field, petrographic, mineral, and whole-rock chemistry and pressure–temperature estimates, suggest three main sources for these mantle xenoliths: garnet-free websterite xenoliths derived from a source region with low P and T (16 kbar, 1065 °C) and MORB isotopic signature, ⁸⁷Sr/⁸⁶Sr ratio of 0.7030, and ¹⁴³Nd/¹⁴⁴Nd ratio of 0.5129. Garnet-bearing peridotite and websterite xenoliths derived from two different sources in the mantle: i) a source with intermediate P and T (29–35 kbar, 1250–1295 °C) conditions, similar to that of sub-oceanic geotherm, with an OIB isotopic signature (⁸⁷Sr/⁸⁶Sr ratio of 0.7043 and ¹⁴³Nd/¹⁴⁴Nd ratio of 0.5129); and ii) another source with P and T conditions similar to those of a sub-continental geotherm (>38 kbar, 1140–1175 °C) and OIB isotopic characteristics (⁸⁷Sr/⁸⁶Sr ratio=0.7041 and ¹⁴³Nd/¹⁴⁴Nd ratio=0.5135).     

The mafic-ultramafic complex near Finero (Ivrea-Verbano Zone), II. Geochronology and isotope geochemistry

Whole-rock Nd and Sr isotopic compositions of the mafic-ultramafic complex near Finero demonstrate that the magma was derived from a depleted, perhaps MORB-type mantle reservoir. The Sm-Nd data for the Amphibole Peridotite unit can be interpreted as an isochron with an apparent age of 533 ± 20 Ma, which is consistent with a ²⁰⁷Pb/²⁰⁶Pb evaporation age of 549 ± 12 Ma of a single zircon grain from the Internal Gabbro unit. However, the interpretation of these apparent ages remains open to question. We therefore retain the alternative hypotheses that the intrusion occurred either about 533 or 270 Ma ago, the latter being the most likely age of emplacement of the much larger magma body near Balmuccia (Val Sesia). The implication of the older emplacement age (if correct) would be that the igneous complex may be related to the numerous amphibolite units, which are intercalated with the metapelites of the overlying Kinzigite Formation, and together with them may constitute an accretionary complex. In this case, the mafic-ultramafic complex itself might also be part of such an accretionary complex (as has been proposed for the Balmuccia peridotite).

Internal Sm-Nd isochrons involving grt, cpx, plag and amph from the Internal Gabbro unit yield concordant ages of 231 ± 23, 226 ± 7, 223 ± 10, 214 ± 17, and 203 ± 13 Ma. These results confirm published evidence for a separate, regional heating event about 215 ± 15 Ma ago.

Initial _Nd(533) values average +6.3 ± 0.4 for six samples of the Amphibole Peridotite unit and +6.0 ± 1.2 for ten samples of the External Gabbro unit. ⁸⁷Sr/⁸⁶Sr ratios require little or no age correction and range from 0.7026 to 0.7047 (with two outliers at 0.7053 and 0.7071). Strong correlations between ⁸⁷Sr/⁸⁶Sr and K₂O and weaker correlations between initial _Nd and K₂O imply a comparatively minor (≤ 10%) contamination of the External Gabbro magma by crustal material and a later alteration by a crustal or seawater-derived fluid. These results contrast sharply with the isotopic composition (negative _Nd and high ⁸⁷Sr/⁸⁶Sr values) of the associated mantle rocks, the Phlogopite Peridotite unit, which has been pervasively metasomatized by crustal fluids. This type of metasomatism and its isotopic signature are never seen in the magmatic complex. This evidence rules out any direct genetic relationship between the igneous complex and the mantle peridotite. The crust-mantle interaction is the opposite of that seen at Balmuccia, where the mantle peridotite is essentially ‘pristine’ and the magmatic body has been extensively contaminated by assimilation of crustal rocks.     

Geochemical constraints on the origin of bimodal magmatism at the Okinawa Trough, an incipient back-arc basin

The magmatism at the axial zone of the middle Okinawa Trough, a young continental back-arc basin, comprises a bimodal basaltic–rhyolitic suite, accompanied by minor intermediate rocks. We report major and trace element and Sr–Nd isotopic data for the intermediate to silicic suites, to provide constraints on their petrogenesis. The rhyolites, recovered as lava and pumice, fall into three geochemical groups (type 1, 2, and 3 rhyolites). Type 1 rhyolites have ⁸⁷Sr/⁸⁶Sr (0.7040–0.7042) and ¹⁴³Nd/¹⁴⁴Nd (0.5128–0.5129) identical to those of associated basalts, and are characterized by highly fractionated REE patterns. Petrogenesis of type 1 rhyolites is explicable in terms of fractional crystallization of the associated basalt. In contrast, type 2 rhyolites and andesite have slightly higher ⁸⁷Sr/⁸⁶Sr (0.7044–0.7047) but similar ¹⁴³Nd/¹⁴⁴Nd (0.5128) compared to those of the basalts. The compositions of type 2 rhyolite and andesite can be explained by assimilation and fractional crystallization (AFC) processes of the basalt magma; quantitative analysis suggests assimilation/fractional crystallization (M_a/M_c) ratios of ≤0.05. Hybrid andesite generated by mixing of evolved basalt and type 1 rhyolite is also present. We emphasize that mechanical extension in this part of the Okinawa Trough involves gabbroic lower crust that resulted from fractionation of mantle-derived basaltic magmas. Type 3 rhyolite occurs only as pumice, which makes its derivation questionable. This rhyolite has major and trace element compositions and Sr–Nd isotopic ratios, which suggests that it may be derived from volcanic activity on the southern Ryukyu volcanic front, and arrived in the Okinawa Trough by drifting on the Kuroshio Current.     

铷同位素分析方法及研究进展

Rb作为一个具有中度挥发性、流体活动性、在岩浆过程中呈不相容性的碱金属元素,能为各种地质过程和物质源区提供制约;同时,⁸⁷Rb是放射性母体,Rb-Sr定年体系在确定长时间尺度的地质体年龄方面也有广泛的应用。传统研究认为特定地质年代下Rb同位素比值(⁸⁷Rb/⁸⁵Rb)是一个定值,但随着分离纯化方法的改进和质谱分析精度的提高,高精度Rb同位素组成得以测定,其结果显示,不同地质样品存在明显的Rb同位素组成的差异,意味着地质过程中存在Rb同位素的分馏。Rb同位素分馏能否为示踪Rb的地质过程提供更多有用信息,是否会对传统Rb-Sr定年体系产生影响,这些基础性的问题目前仍然没有答案。要回答这些问题,首先需要了解不同地质储库的Rb同位素组成,发现不同地质过程中的Rb同位素分馏,探讨其发生的控制机制。然而,这方面的研究目前还非常欠缺。文章回顾了近20年来国际上地球科学领域中的Rb同位素已有的研究,包括技术方法、分馏机理等各个方面,在此基础上对其研究前景进行展望,主要包括:(1)总结了Rb同位素组成测定的化学纯化及仪器测量方法,并对其优缺点进行点评,同时指出谨慎的化学前处理方法及质谱测定流程是获得高精度Rb同位素组成结果的基本前提;(2)收集了现有的地外样品Rb同位素组成数据,简述了Rb同位素在宇宙化学中的应用研究成果,指出Rb作为一个中度挥发性元素,对太阳系行星的吸积和演化过程具有重要的指示意义;(3)对Rb同位素在地质过程中潜在广阔的应用前景进行展望,例如完善经典的Rb-Sr定年体系,限定壳幔及地壳内部的分异过程,制约大陆硅酸盐岩风化,以及揭示超大型Rb矿的形成机制。     

GBW10010a大米标准物质复(研)制及数据特征

随着我国对生态文明建设的重视，自然资源综合调查势在必行，对生物标准物质亦提出了新的需求。当前相关调研工作已经大面积开展，自然资源综合调查、农产品与食品安全评价都需要对生物样品元素组成进行准确测试，需要以生物标准物质作为生物成分测试量值比对和溯源的基础，因此对生物基体标准物质的需求量大幅增加。大米作为主要粮食之一，其食品安全日益受到重视，对大米中的化学成分进行准确的分析测试具有重要的现实意义，因而对大米标准物质的需求量尤为突出，但目前大米成分分析标准物质已供不应求。本文严格按照《标准物质定值的通用原则及统计学原理》（JJF 1343—2012）和《地质分析标准物质的研制》（JJF 1646—2017）等相关规范要求，开展了GBW10010a大米成分分析标准物质的复（研）制工作，包括样品采集、加工制备、均匀性检验、稳定性检验、多家实验室协作定值测试及不确定度评定等关键环节。结果表明：本次复（研）制的大米标准物质定值成分多样、量值准确可靠，符合国家一级标准物质的要求。GBW10010a共定值54项主微量元素，包括Ag、Al、As、B、Ba、Be、Bi、Ca、Cd、Ce、Co、Cr、Cs、Cu、Dy、Er、Eu、Fe、Gd、Ge、Hg、Ho、K、La、Li、Ho、Mg、Mn、Mo、N、Na、Nb、Nd、Ni、P、Pb、Pr、Rb、S、Sb、Sc、Se、Si、Sm、Sr、Tb、Th、Tl、Tm、U、V、Y、Yb、Zn，其中的39项元素给出了标准值及不确定度，包括Ag、Al、As、B、Ba、Ca、Cd、Ce、Co、Cs、Cu、Dy、Er、Fe、Hg、K、Li、Mg、Mn、Mo、N、Na、Nd、Ni、P、Pb、Pr、Rb、S、Sb、Se、Si、Sm、Sr、Tb、Tl、Y、Yb、Zn；15项元素提供参考值，包括Be、Bi、Cr、Eu、Gd、Ge、Ho、Ho、La、Nb、Sc、Th、Tm、U、V。与原有GBW10010大米标准物质相比较，GBW10010a中As、Cd、Co、Cr、Cu、Hg、Mn、Mo、Ni、Zn等重金属元素含量显著下降，其中Cd、Cu、Zn降幅较大，分别下降约39%、43%、38.7%，一定程度上反映了农田生态环境的改善。本批标准物质定值元素总数量增加了6项，新增定值元素Ag、Nb（Nb给出参考值），并且各项元素不确定度范围整体上有所缩小，如Al、Cd、Cu、Fe、K、Mg、Mo、Na、P、Pb、Se、Zn等对生物易有影响的重要元素，表明了地质分析测试方法技术的进步及定值水平的提高。本批标准物质定值元素涵盖了具有生物效应的大部分主微量元素，适用于农业生态环境地球化学调查与评价、生物样品测试、农产品质量与食品安全评价样品测试时的分析仪器校正、分析方法评价和分析质量监控等多个领域。     

He, Sr, Nd, and Pb isotopic constraints on the origin of the Marquesas and other linear volcanic chains

The classic hotspot hypothesis [Morgan, W. J., 1971. Convection plumes in the lower mantle. Nature 230, 42–43], which posits that linear volcanic chains are traces of fixed plumes in the mantle on moving lithospheric plates, was instrumental in elevating the plate tectonics paradigm in the 1960s into a modern Earth Science theory. The hypothesis itself, however, remains conjectural because many of its predictions, particularly the simple age-progressive type of volcanism, are not observed in many linear volcanic chains. As an alternative explanation, it is proposed that linear volcanic chains are formed through magmatism along pre-existing lines of weakness such as transform zones and old sutures, or along cracks created by stresses on lithospheric plates. The Marquesas linear volcanic chain in south-central Pacific has geologic features that are consistent with some of the predictions of both hypotheses. To better constrain the origin of this volcanic chain, we collected major and trace element and Sr, Nd, Pb, and He isotopic data from several Marquesan lavas. Our new analyses combined with literature data classify the samples into the well established tholeiitic to mildly alkalic, low ⁸⁷Sr/⁸⁶Sr, high ¹⁴³Nd/¹⁴⁴Nd, shield-building volcanic phase lava group and highly alkalic, high ⁸⁷Sr/⁸⁶Sr, low ¹⁴³Nd/¹⁴⁴Nd, post-shield phase group. Lead isotopes show generally higher ²⁰⁶Pb/²⁰⁴Pb ratios and suggest evidence of crustal assimilation for the shield-building phase lavas, consistent with the argument that the shield-building phase volcanism has a lithospheric source component. On the other hand, post-shield phase lavas that are predicted to represent the true composition of the mantle source by the hotspot hypothesis have higher ³He/⁴He ratios and these are coupled to other geochemical tracers. Thus our results show that the Marquesas volcanic chain, similar to many other linear volcanic chains, has a high ³He/⁴He component in its mantle source. The presence of such a distinct source component cannot be easily explained by dispersed upper mantle heterogeneities, but provides a powerful constraint for the hotspot origin of many linear volcanic chains.     

Petrology and Geochemistry of the Volcanic Rocks Dredged from the Geophysicist Seamount in the Kurile Basin: Evidence for the Existence of Thinned Continental Crust

Dredged samples from the Geophysicist seamount volcano in the northeastern part of the Kurile Basin include volcanic and volcanoclastic rocks ranging from basalt to andesite. The rocks have geochemical features typical of high-K island-arc calc-alkaline volcanism. They are enriched in LILE and depleted in Zr, Ti, Nb, Ta and Y. The chondrite-normalized REE patterns are characterized by enrichment of LREE similar to those of island-arc lava from the submarine volcanoes of rear-arc zone of the Kurile Island Arc. The volcanic rocks have a wide range of ⁸⁷Sr/⁸⁶Sr ratios (0.70287-0.70652), varying ¹⁴³Nd/¹⁴⁴Nd and Pb isotopic ratios. Their trace-element compositions and Sr-Nd-Pb isotope signatures may be explained by a small addition of crustal continental component to mantle-derived magmas that suggest the existence of thinned continental basement under the eastern part of the Kurile Basin.     

Andean subduction-related mantle xenoliths: Isotopic evidence of Sr–Nd decoupling during metasomatism

Sr–Nd isotopic analyses on some mantle xenolith samples from the Northern, Southern and Austral Andean volcanic zones exhibit radiogenic Sr enrichment without dramatic changing of the Nd isotopic composition. This anomalous effect (Sr–Nd decoupling) makes these samples plot displaced to the right side of the “mantle array” trend (here called the “MORB–OIB–BSE trend”) in the ⁸⁷Sr/⁸⁶Sr vs. ¹⁴³Nd/¹⁴⁴Nd isotopic diagram. Such behavior reflects processes that took place in the mantle and can be related to: i) the mixture of a depleted mantle and an enriched source (enriched mantle II—EMII); ii) the mixture of a depleted mantle and a mixture of mantle-derived and slab-derived melts; and iii) a chromatographic process that occurs during the percolation of a metasomatic agent through the mantle.