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1.
安徽女山橄榄岩包体的氧同位素比值和微量元素组成：地幔交代作用 总被引：6，自引：4，他引：6
本文的研究对象是9个来自安徽女山新生代玄武岩的橄榄岩包体,利用激光氟化技术系统分析了橄榄石、单斜辉石和斜方辉石的氧同位素比值;利用LA-ICPMS技术分析了单斜辉石的微量元素组成。结果显示,女山橄榄岩存在辉石与橄榄石之间的氧同位素不平衡分馏现象,其中△Cpx-Ol18O(=δ18OCpx-δ18OOl)出现低至-0．5‰的负值;含角闪石包体中的单斜辉石明显富集大离子亲石元素(LILE,如Sr、Th、LREE)和亏损高场强元素(HFSE,如Nb、Zr、Ti)。氧同位素的数据表明,女山上地幔曾经经历过俯冲洋壳流体参与的交代作用,根据单斜辉石和橄榄石之间氧同位素分馏值△Cpx-Ol18O与包体形成深度之间的负相关性,提出了一个“上升 缓冲”的流体交代模型。虽然微量元素特征也表明女山上地幔受到过地壳流体的影响,但是氧同位素的不平衡分馏和LILE的富集／HFSE的亏损并不是同步的,对这种现象的可能解释是:引起氧同位素不平衡分馏的交代作用和造成女山单斜辉石微量元素特征的交代作用不是同一期的,即女山上地幔曾经发生过至少2次交代事件。 相似文献
2.
离子探针Li同位素微区原位分析技术与应用 总被引：1，自引：0，他引：1
Li同位素是一种新兴的非传统稳定同位素示踪工具,其应用领域涵盖了从地表到地幔的熔/流体与矿物之间的相互作用以及行星的早期演化研究。随着多接收器电感耦合等离子体质谱仪(MC ICPMS)和二次离子质谱仪(SIMS)技术的迅速发展,锂同位素地球化学研究取得了长足进步和发展。Cameca IMS 1280 SIMS可以在约20 μm×30 μm×2 μm的空间尺度上获得约1‰(1σ)的分析精度,实现了高精度微区原位Li同位素分析。由于Li同位素基体效应明显,获取与分析样品基体匹配的标准样品对Li同位素分析的准确性尤为关键。在重点介绍SIMS微区原位Li同位素分析技术的基础上,以锆石、橄榄石和辉石为例,综述了Li同位素原位分析技术的最新应用研究进展及存在的问题,旨在加深对Li同位素原位分析技术的理解,展示其在地球化学研究中的良好应用前景。 相似文献
3.
对滇东南马关火山爆砾岩筒以及玄武岩中的单斜辉石巨晶进行了主量元素、微量元素、原位Sr同位素以及含水性研究,结果显示,单斜辉石巨晶均为铝质普通辉石,Mg#与Al、Fe、Ti呈负相关,与Ca呈正相关;稀土元素总量不高,HREE及LREE亏损,而MREE相对富集,大离子亲石元素均出现明显亏损,高场强元素Nb、Zr出现亏损而Hf略富集,Nb、Ta与Zr、Hf分馏明显,Rb、Ba的变化范围较大。原位Sr同位素87Sr/86Sr值为0. 703 92～0. 705 06,巨晶单斜辉石来源于上地幔,形成于同一母岩浆,与寄主玄武岩同源,为源岩浆在高压下的结晶产物。运用显微红外-傅里叶变换红外光谱仪(Micro-FTIR)分析测试了单斜辉石巨晶的水含量,结果显示OH吸收峰位于3 700～2 800cm-1,含水量赋值范围为318×10-6～693×10-6,水含量稍富于女山及汉诺坝地区的单斜辉石巨晶,也高于马关地区幔源橄榄岩包体中的单斜辉石结构水含量,暗示该区上地幔岩石圈具高含水性,这同时证实了俯冲洋壳在研究区的活动。新近纪到达地幔过渡带的西太平洋洋壳俯冲发生转向东撤,此时新特提斯洋洋壳正在NE向俯冲,是马关地区深部地幔富水的主因,到达软流圈(或地幔过渡带)的新特提斯洋俯冲洋壳导致该区地幔熔融,岩浆随之而生。 相似文献
4.
雅鲁藏布江缝合带西段普兰蛇绿岩中地幔橄榄岩的岩石学研究 总被引：14，自引：10，他引：4
西藏雅鲁藏布江缝合带西段普兰蛇绿岩以出现面积约600余平方千米的特大型地幔橄榄岩体而引人注目.该地幔橄榄岩以方辉橄榄岩为主体,含有少量的二辉橄榄岩和纯橄榄岩,岩体中另有一些橄榄单斜辉石岩、辉长岩和辉绿岩等侵入体.地幔橄榄岩的主要造岩矿物橄榄石的Fo 90～93,其中呈包裹体的橄榄石的Fo略高,斜方辉石为顽火辉石(En 88～90),单斜辉石主要为顽透辉石和透辉石,以低铝(0.48％～3.96％)和高Mg#(91～96)为特征,铬尖晶石的Cr#值为18～69,其中方辉橄榄岩和二辉橄榄岩中的铬尖晶石属富铝型尖晶石,而纯橄岩中为富铬型尖晶石.橄榄单斜辉石岩的橄榄石Fo值一致较低,平均为88.4,斜方辉石En平均87,单斜辉石以透辉石为主,铬尖晶石的Cr#值为45～69.普兰地幔橄榄岩及橄榄单斜辉石岩都具有相似的稀土元素和微量元素配分模式,表现为LREE相对富集,Eu亏损不明显,微量元素中大离子亲石元素含量较低,部分样品高场强元素亏损,另一些则相对富集,显示地幔橄榄岩具有亏损地幔源区特征,但也具有俯冲带流体的交代特征,表明普兰岩体可能经历了MOR和SSZ两种构造环境,该特征与雅鲁藏布江缝合带东段的罗布莎地幔橄榄岩的特征可以对比. 相似文献
5.
长白山地区位于华北克拉通东北部,广泛出露富含地幔橄榄岩包体的新生代玄武岩,为研究岩石圈地幔的性质和演化提供了优越条件。本文对长白山地区天池和龙岗新生代火山岩群中尖晶石相橄榄岩包体进行了岩石学、全岩主微量元素、矿物主量元素、单斜辉石微量元素和Sr-Nd-Hf同位素分析。研究结果表明,尖晶石相橄榄岩包体由二辉橄榄岩和少量的方辉橄榄岩组成,Mg#值为87.4～91.2,表现出新生饱满的特征,平衡温度为900～1100℃。橄榄石的Mg#值(%Fo)为85.6～91.3。单斜辉石包括四种类型:(1)轻稀土元素严重亏损型;(2)轻稀土元素亏损型;(3)向右微倾型和(4)"勺型"。单斜辉石表现出Sr同位素(87Sr/86Sr=0.702749～0.707276)整体亏损,部分样品富集的特征,单斜辉石的Nd-Hf同位素呈现出亏损特征(143Nd/144Nd=0.512886～0.51333、εHf=+17.7～+49.8)。长白山地区二辉和方辉橄榄岩分别经历了小于10%和略大于10%的部分熔融作用,并受到富水硅酸盐熔体的地幔交代作用。太平洋板块向西俯冲作用使得软流圈上涌并携带大量壳源物质进入地幔深部,与岩石圈地幔发生橄榄岩-熔体反应,形成了长白山地区不均一的岩石圈地幔,以新增生饱满地幔为主,夹有少量古老难熔岩石圈地幔碎片。 相似文献
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穿地壳岩浆系统理念的提出为认知岩浆岩的形成机制提供了一个新的窗口。在穿地壳岩浆系统内,深层次岩浆储库结晶的矿物(例如辉石、角闪石、斜长石等)可通过通道向上运移至浅层次的岩浆储库,该过程可导致这些矿物的熔蚀、流体交代或再生长。上述矿物属于再循环晶,它们保留的成分环带信息可忠实地记录岩浆环境的变化。本文以华北克拉通东南缘胶北早白垩世丛家岩体(-127Ma)内产出的闪斜-拉辉煌斑岩为主要研究对象。这些钙碱性煌斑岩中常见不同结构和成分特征的单斜辉石再循环晶,它们保存了多级岩浆储库的相关信息。丛家煌斑岩包括一系列中基性煌斑岩,形成一个煌斑岩岩石组合具有轻重稀土元素分异明显((La/Yb)_N=14.2～28.1)的特征。在原始地幔标准化微量元素蜘蛛图上丛家煌斑岩表现出亏损Nb、Ta、P和Ti,而富集Ba、Pb、Sr和Nd等元素的特征。本文在丛家煌斑岩中识别出了两类单斜辉石"再循环晶"即正环带单斜辉石和振荡环带单斜辉石。正环带辉石核部Mg~#值为86.0～94.9,稀土元素总含量偏低,亏损HREE;部分核部具筛状结构,筛孔填充物富集大离子亲石元素,并表现出Cr-Ni元素的解耦,显示与流体交代作用有关。正环带辉石边部具振荡环带特征,反映了晶体在震荡环境中的再生长。再生长辉石环带的Mg~#值为78.9～89.1稀土元素总含量较高,但其分配趋势与核部相似,富集Th等元素,亏损Nb、Pb、P。振荡环带辉石的Mg~#值为82.3～89.4,化学成分特征与正环带辉石边部相近。丛家煌斑岩中的角闪石可分为低硅角闪石和高硅角闪石。低硅角闪石的SiO_2含量偏低(38.2%～40.1%),Mg~#值为72.0～82.4,结晶于较高的温压环境(976±22℃～1024+22℃,5.72～10.9kbar)。高硅角闪石的SiO_2含量较高(40.3%～44.3%)Mg~#值为70.9～83.0,结晶于相对低的温压环境(872±22℃～947±22℃,3.06～4.43kbar)。本研究认为,丛家煌斑岩中的单斜辉石再循环晶在不同层次岩浆储库内发生了熔蚀、流体交代或再生长,指示了深部岩浆系统是由多级岩浆储库构成的。 相似文献
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达拉布特蛇绿岩位于中亚造山带西南缘,是古亚洲洋的扩张、俯冲、消减和闭合过程的产物,保留了洋盆形成及构造演化信息。前人对达拉布特蛇绿岩的形成大地构造背景始终未取得统一的认识。为探讨蛇绿岩所代表的构造演化过程,笔者以达拉布特蛇绿岩中的地幔橄榄岩为研究对象,通过详细的矿物地球化学及其氧同位素研究,对达拉布特地幔橄榄岩成因及构造背景提出新的制约。达拉布特方辉橄榄岩中橄榄石Ni/Co值为21~22,Ni/Mn值为3.0~7.8具有部分熔融残余的特征,此外,橄榄石中不相容元素相对于正常地幔橄榄石亏损,表明方辉橄榄岩为部分熔融的残余组分。方辉橄榄岩中尖晶石Cr# 为47~52、TiO2含量0.01%~0.04%,橄榄石Fo为90.34%~90.98%指示方辉橄榄岩经历>20%的部分熔融。方辉橄榄岩中橄榄石δ18 Oolivine值+5.1~+6.2‰、单斜辉石δ18Ocpx值+5.6~+6.9‰,其变化范围较大且整体高于正常地幔中橄榄石和单斜辉石的δ18 O值,矿物间氧同位素分馏系数Δ18OOpx—olivine平均-0.3‰,Δ18OOpx—cpx平均-0.7‰,显著区别于正常地幔中平衡的氧同位素分馏系数,具有明显的交代作用特征。结合方辉橄榄岩橄榄石中亏损的微量元素特征,认为方辉橄榄岩可能受到流体交代作用的影响,俯冲壳源物质脱水形成的高δ18O流体交代地幔橄榄岩导致了矿物与矿物间不平衡的氧同位素特征。通过尖晶石与单斜辉石成分判别,尖晶石与单斜辉石的主量元素具有介于弧前与深海地幔之间的过渡型特征,与俯冲初始阶段形成的地幔橄榄岩相似。综合矿物地球化学与氧同位素特征,笔者认为达拉布特地幔橄榄岩为形成于弧前初始俯冲环境。板块俯冲导致弧前扩张形成新洋壳,上涌的软流圈MORB like熔体与俯冲壳源物质熔融形成熔/流体与地幔橄榄岩相互作用,形成达拉布特地幔橄榄岩。 相似文献
8.
达拉布特蛇绿岩位于中亚造山带西南缘,是古亚洲洋的扩张、俯冲、消减和闭合过程的产物,保留了洋盆形成及构造演化信息。前人对达拉布特蛇绿岩的形成大地构造背景始终未取得统一的认识。为探讨蛇绿岩所代表的构造演化过程,笔者以达拉布特蛇绿岩中的地幔橄榄岩为研究对象,通过详细的矿物地球化学及其氧同位素研究,对达拉布特地幔橄榄岩成因及构造背景提出新的制约。达拉布特方辉橄榄岩中橄榄石Ni/Co值为21~22,Ni/Mn值为3.0~7.8具有部分熔融残余的特征,此外,橄榄石中不相容元素相对于正常地幔橄榄石亏损,表明方辉橄榄岩为部分熔融的残余组分。方辉橄榄岩中尖晶石Cr# 为47~52、TiO2含量0.01%~0.04%,橄榄石Fo为90.34%~90.98%指示方辉橄榄岩经历>20%的部分熔融。方辉橄榄岩中橄榄石δ18 Oolivine值+5.1~+6.2‰、单斜辉石δ18Ocpx值+5.6~+6.9‰,其变化范围较大且整体高于正常地幔中橄榄石和单斜辉石的δ18 O值,矿物间氧同位素分馏系数Δ18OOpx—olivine平均-0.3‰,Δ18OOpx—cpx平均-0.7‰,显著区别于正常地幔中平衡的氧同位素分馏系数,具有明显的交代作用特征。结合方辉橄榄岩橄榄石中亏损的微量元素特征,认为方辉橄榄岩可能受到流体交代作用的影响,俯冲壳源物质脱水形成的高δ18O流体交代地幔橄榄岩导致了矿物与矿物间不平衡的氧同位素特征。通过尖晶石与单斜辉石成分判别,尖晶石与单斜辉石的主量元素具有介于弧前与深海地幔之间的过渡型特征,与俯冲初始阶段形成的地幔橄榄岩相似。综合矿物地球化学与氧同位素特征,笔者认为达拉布特地幔橄榄岩为形成于弧前初始俯冲环境。板块俯冲导致弧前扩张形成新洋壳,上涌的软流圈MORB like熔体与俯冲壳源物质熔融形成熔/流体与地幔橄榄岩相互作用,形成达拉布特地幔橄榄岩。 相似文献
9.
南海新生代玄武岩中单斜辉石地球化学特征
及其地质意义 总被引：2，自引：0，他引：2
南海新生代玄武岩中发育有大量的单斜辉石斑晶,与橄榄石、角闪石等斑晶共存,多数被熔蚀,呈浑圆状,部分发育有很窄的反应边。研究表明单斜辉石具有巨晶的特征,是在高压下在与寄主岩同源的岩浆中形成,没有经历长时间的沉淀生长而直接向上运移被带到地表,因而具有巨晶的主量及微量元素的特征却不具有巨晶的形态。单斜辉石稀土元素含量不高,HREE及LREE亏损,而MREE富集;大离子亲石元素Rb、Ba、Sr均出现明显的亏损,高场强元素Nb、Zr出现亏损而Hf略富集。Nb、Ta与Zr、Hf分馏明显。Th较为富集,而Pb强烈亏损,U的变化范围较大。研究发现南海新生代玄武岩中的单斜辉石的来源较为简单,为地幔柱的直接产物,并没有受到洋中脊—地幔柱相互作用的影响,由于岩浆上升速度较快压力迅速下降,橄榄石大量晶出,引起了岩浆成分的变化,致使单斜辉石与寄主岩成分和结构上没有达到平衡。 相似文献
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Carbon,sulfur, oxygen and strontium isotope records,organic geochemistry and biostratigraphy across the Permian/Triassic boundary in Abadeh,Iran 总被引：6，自引：0，他引：6
Pelagic deposits at Abadeh represent a complete biostratigraphic record across the Permian/Triassic boundary (PTB). The presumed water depth during deposition of these sediments was between 60 and 90 m. Similar to other Permian/Triassic boundary sections, the succession at Abadeh is characterised by a negative carbon isotope shift of approximately 4. The values start to decrease in the lower C. changxingensis - C. deflecta s.l. Zone, reach –0.12 (V-PDB) in the uppermost Permian just below the PTB, remain low to the early I. isarcica Zone (–0.32) and increase subsequently in the upper I. isarcica Zone. For the time interval of the PTB negative carbon isotope excursion, between the C. iranica and the I. isarcica Zones, no correlation exists between the 13Ccarb and the 18Ocarb. The above observations argue against the conclusion of Heydari et al. (2001) that the carbon isotope event at the P/T transition is an alteration artefact and not a global signal. The decrease in 13Ccarb is accompanied by a ~5 (and potentially up to 10) increase in 34SSSS. Together, these features are thought to reflect a complex global event, notably the development of widespread anoxic oceans with anoxic bottom layers rising onto the shelves. For the carbon isotope drop, other factors, such as the collapse of ocean primary productivity may also have played a role. The 87Sr/86Sr ratios of Dzhulfian seawater show only a minor increase from 0.70705 to 0.70710, reaching 0.70720 in the Dorashamian. The increase becomes steeper in the Early Triassic reaching 0.70754 in the N. dieneri Zone. The rise of the strontium isotope values is thought to be related to enhanced continental weathering under humid climatic conditions in the uppermost Permian (C. meishanensis - H. praeparvus Zone) and the lack of a dense land vegetation in the Early Triassic, prior to the Spathian (Upper Olenekian). 相似文献
12.
Subías I. Yuste A. Fanlo I. Fernández-Nieto C. González López J.M. 《Geologie en Mijnbouw》1999,78(1):87-102
Mineralogical, textural and geochemical investigations were made to determine the post-depositional evolution of Devonian and Early Carboniferous carbonates from Valle de Tena. The carbonate association is made up of low-Mg calcite, which occurs as micrite, spar cements, neomorphic patches and spar filling veinlets. Non-stoichiometric dolomite and ankerite occur as cements (dolomite also as replacements) in the Middle Devonian, post-dating calcite types. All these phases pre-date tectonic stylolites, indicating compaction after stabilization of the carbonate minerals. Strontium concentrations indicate that Early Devonian and Early Carboniferous micrites initially precipitated as aragonite; Middle and Late Devonian micrites precipitated as high-Mg calcites. Both precursors were diagenetically stabilized to low-Mg calcites through interaction with meteoric waters in phreatic environments. Trace elements in dolomite and ankerite indicate precipitation from Sr-enriched meteoric water. All studied carbonates, except Middle Devonian limestones, precipitated in reducing environments, which favoured incorporation of Fe and Mn. Late calcite generations precipitated from more saline waters than micrites. Light 18O values in micrites suggest alteration mainly in meteoric-phreatic environments. The dolomites and ankerites precipitated from more 18O-depleted fluids than the calcites, suggesting a greater contribution from meteoric waters. Variations in 13C of micrites represent primary secular trends, according to published 13C variations. The 13C oscillations within each succession probably relate to sea-level oscillations. Strontium isotopes also point to a meteoric origin of diagenetic fluids. Model calculations suggest that O and Sr isotopes equilibrated between calcites and fluid at relatively low water/rock ratios, whereas C isotopic signatures are inherited from limestones. 相似文献
13.
镁同位素地球化学研究新进展及其应用 总被引：7，自引：3，他引：4
作为一种新兴的地质示踪剂,Mg同位素正受到国际地学界日益广泛的关注。Mg同位素地球化学研究已取得了巨大的进展,近期研究工作主要包括两个方面。首先,调查了地球各主要储库和陨石的Mg同位素组成特征,结果表明陨石和地球地幔具有均一并且相似的Mg同位素组成,平均δ26Mg值分别为-0.28±0.06‰和-0.25±0.07‰;相反,上地壳和水圈的Mg同位素组成很不均一,δ26Mg值变化范围分别为-4.84‰~+0.92‰和-2.93‰~+1.13‰。其次,对一些地质和物理化学过程中Mg同位素的分馏行为进行研究,结果表明:(1)地表风化作用可以造成大的Mg同位素分馏,导致重Mg同位素残留在风化产物中而轻Mg同位素进入水圈;(2)岩浆分异过程中Mg同位素平衡分馏很小;(3)高温化学扩散和热扩散过程中Mg同位素会发生显著的动力学分馏。基于这些研究成果,Mg同位素体系已经被初步应用于示踪早期地球形成和壳内物质再循环等过程,并有望在不久的将来应用于示踪大陆地壳的化学演化和地质温度计等研究领域。 相似文献
14.
Frédéric Moynier Toshiyuki Fujii Kun Wang Julien Foriel 《Comptes Rendus Geoscience》2013,345(5-6):230-240
Iron is one of the most abundant transition metal in higher plants and variations in its isotopic compositions can be used to trace its utilization. In order to better understand the effect of plant-induced isotopic fractionation on the global Fe cycling, we have estimated by quantum chemical calculations the magnitude of the isotopic fractionation between different Fe species relevant to the transport and storage of Fe in higher plants: Fe(II)-citrate, Fe(III)-citrate, Fe(II)-nicotianamine, and Fe(III)-phytosiderophore. The ab initio calculations show firstly, that Fe(II)-nicotianamine is ～3‰ (56Fe/54Fe) isotopically lighter than Fe(III)-phytosiderophore; secondly, even in the absence of redox changes of Fe, change in the speciation alone can create up to ～1.5‰ isotopic fractionation. For example, Fe(III)-phytosiderophore is up to 1.5‰ heavier than Fe(III)-citrate2 and Fe(II)-nicotianamine is up to 1‰ heavier than Fe(II)-citrate. In addition, in order to better understand the Fe isotopic fractionation between different plant components, we have analyzed the iron isotopic composition of different organs (roots, seeds, germinated seeds, leaves and stems) from six species of higher plants: the dicot lentil (Lens culinaris), and the graminaceous monocots Virginia wild rye (Elymus virginicus), Johnsongrass (Sorghum halepense), Kentucky bluegrass (Poa pratensis), river oat (Uniola latifolia), and Indian goosegrass (Eleusine indica). The calculations may explain that the roots of strategy-II plants (Fe(III)-phytosiderophore) are isotopically heavier (by about 1‰ for the δ56Fe) than the upper parts of the plants (Fe transported as Fe(III)-citrate in the xylem or Fe(II)-nicotianamine in the phloem). In addition, we suggest that the isotopic variations observed between younger and older leaves could be explained by mixing of Fe received from the xylem and the phloem. 相似文献
15.
Sean T. Murray John A. Higgins Chris Holmden Chaojin Lu Peter K. Swart 《Sedimentology》2021,68(1):1-29
In an effort to constrain the mechanism of dolomitization in Neogene dolomites in the Bahamas and improve understanding of the use of chemostratigraphic tracers in shallow‐water carbonate sediments the δ34S, Δ47, δ13C, δ18O, δ44/40Ca and δ26Mg values and Sr concentrations have been measured in dolomitized intervals from the Clino core, drilled on the margin of Great Bahama Bank and two other cores (Unda and San Salvador) in the Bahamas. The Unda and San Salvador cores have massively dolomitized intervals that have carbonate associated sulphate δ34S values similar to those found in contemporaneous seawater and δ44/40Ca, δ26Mg values, Sr contents and Δ47 temperatures (25 to 30°C) indicating relatively shallow dolomitization in a fluid‐buffered system. In contrast, dolomitized intervals in the Clino core have elevated values of carbonate associated sulphate δ34S values indicating dolomitization in a more sediment‐buffered diagenetic system where bacterial sulphate reduction enriches the residual in 34S, consistent with high sediment Sr concentrations and low δ44/40Ca and high δ26Mg values. Only dolomites associated with hardgrounds in the Clino core have carbonate associated δ34S values similar to seawater, indicating continuous flushing of the upper layers of the sediment by seawater during sedimentary hiatuses. This interpretation is supported by changes to more positive δ44/40Ca values at hardground surfaces. All dolomites, whether they formed in an open fluid‐buffered or closed sediment‐buffered diagenetic system have similar δ26Mg values suggesting that the HMC transformed to dolomite. The clumped isotope derived temperatures in the dolomitized intervals in Clino yield temperatures that are higher than normal, possibly indicating a kinetic isotope effect on dolomite Δ47 values associated with carbonate formation through bacterial sulphate reduction. The findings of this study highlight the utility of applying multiple geochemical proxies to disentangle the diagenetic history of shallow‐water carbonate sediments and caution against simple interpretations of stratigraphic variability in these geochemical proxies as indicating changes in the global geochemical cycling of these elements in seawater. 相似文献
16.
Jin Li Suo‐han Tang Xiang‐kun Zhu Zhi‐hong Li Shi‐Zhen Li Bin Yan Yue Wang Jian Sun Yao Shi Aiguo Dong Nick S. Belshaw Xingchao Zhang Sheng‐ao Liu Ji‐hua Liu Deli Wang Shao‐yong Jiang KeJun Hou Anthony S. Cohen 《Geostandards and Geoanalytical Research》2019,43(1):163-175
Iron, Cu and Zn stable isotope systems are applied in constraining a variety of geochemical and environmental processes. Secondary reference materials have been developed by the Institute of Geology, Chinese Academy of Geological Sciences (CAGS), in collaboration with other participating laboratories, comprising three solutions (CAGS‐Fe, CAGS‐Cu and CAGS‐Zn) and one basalt (CAGS‐Basalt). These materials exhibit sufficient homogeneity and stability for application in Fe, Cu and Zn isotopic ratio determinations. Reference values were determined by inter‐laboratory analytical comparisons involving up to eight participating laboratories employing MC‐ICP‐MS techniques, based on the unweighted means of submitted results. Isotopic compositions are reported in per mil notation, based on reference materials IRMM‐014 for Fe, NIST SRM 976 for Cu and IRMM‐3702 for Zn. Respective reference values of CAGS‐Fe, CAGS‐Cu and CAGS‐Zn solutions are as follows: δ56Fe = 0.83 ± 0.07 and δ57Fe = 1.20 ± 0.13, δ65Cu = 0.57 ± 0.06, and δ66Zn = ?0.79 ± 0.12 and δ68Zn = ?1.65 ± 0.24, respectively. Those of CAGS‐Basalt are δ56Fe = 0.15 ± 0.07, δ57Fe = 0.22 ± 0.10, δ65Cu = 0.12 ± 0.08, δ66Zn = 0.17 ± 0.13, and δ68Zn = 0.34 ± 0.26 (2s). 相似文献
17.
Climatic and hydrologic variability during the past millennium in the eastern Rocky Mountains and northern Great Plains of western Canada 总被引：1，自引：0，他引：1
Modelling of tree-ring δ13C and δ18O data from the Columbia Icefield area in the eastern Rocky Mountains of western Canada provides fuller understanding of climatic and hydrologic variability over the past 1000 yr in this region, based on reconstruction of changes in growth season atmospheric relative humidity (RHgrs), winter temperature (Twin) and the precipitation δ18O-Twin relation. The Little Ice Age (~ AD 1530s-1890s) is marked by low RHgrs and Twin and a δ18O-Twin relation offset from that of the present, reflecting enhanced meridional circulation and persistent influence of Arctic air masses. Independent proxy hydrologic evidence suggests that snowmelt sustained relatively abundant streamflow at this time in rivers draining the eastern Rockies. In contrast, the early millennium was marked by higher RHgrs and Twin and a δ18O-Twin relation like that of the 20th century, consistent with pervasive influence of Pacific air masses because of strong zonal circulation. Especially mild conditions prevailed during the “Medieval Climate Anomaly” ~ AD 1100-1250, corresponding with evidence for reduced discharge in rivers draining the eastern Rockies and extensive hydrological drought in neighbouring western USA. 相似文献
18.
19.
康定杂岩Rb-Sr、Sm-Nd同位素系统及其意义 总被引：1，自引：0，他引：1
通过对康定—冕宁地区出露的英云闪长岩、黑云角闪斜长片麻岩、角闪变粒岩全岩及其中所分离出的角闪石、黑云母、斜长石、钾长石的Rb-Sr、Sm-Nd同位素的系统测定,结合岩石的锆石U-Pb年龄结果,确定这些变质杂岩由于经历了复杂的形成过程与变质历史,Rb-Sr、Sm-Nd同位素体系难以确定其结晶年龄。由单矿物与全岩Rb-Sr、Sm-Nd体系拟合的~700 M a的等时线年龄反映了角闪岩相-高角闪岩相的变质作用年龄。Sm-Nd同位素体系由于在变质作用过程中的部分开放性,很容易给出无意义的较老的混合年龄。康定杂岩结晶后并没有经历麻粒岩相变质作用,区域上所含的麻粒岩透镜体可能是新元古代(773~721 M a)期间由Rod in ia超大陆裂解产生的新生洋壳向扬子克拉通陆块俯冲消减过程的变质产物。俯冲到一定深度后,由于板片被拉断,软流圈上涌导致变质洋壳板片岩石、先前底侵变质的镁铁质岩石及扬子陆块长英质基底岩石发生部分熔融,以镁铁质岩石熔融产生的熔浆为主(>70%),与长英质基底岩石熔融产生的熔浆混合形成w(Na2O)/w(K2O)>1的TTG组合。 相似文献
20.
Radiogenic isotopes in fluid inclusions 总被引：7，自引：0，他引：7
Radiogenic isotopes studied in fluid inclusions are still a limited field, with great potential for expansion as analytical techniques improve. The main limitation for Sr, Ar and He isotope work is the very small number of radiogenic atoms produced in a typical fluid inclusion. The requirements to analysts are correspondingly high. Examples show that isotopic tracing on fluid inclusion fluids can be a decisive tool in solving geological problems. 相似文献