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Subduction zone geochemistry

机译:俯冲带地球化学

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摘要

Crustal recycling at convergent plate boundaries is essential to mantle heterogeneity.However,crustal signatures in the mantle source of basaltic rocks above subduction zones were primarily incorporated in the form of liquid rather than solid phases.The physicochemical property of liquid phases is determined by the dehydration behavior of crustal rocks at the slab-mantle interface in subduction channels.Because of the significant fractionation in incompatible trace elements but the full inheritance in radiogenic isotopes relative to their crustal sources,the production of liquid phases is crucial to the geochemical transfer from the subducting crust into the mantle.In this process,the stability of specific minerals in subducting crustal rocks exerts a primary control on the enrichment of given trace elements in the liquid phases.For this reason,geochemically enriched oceanic basalts can be categorized into two types in terms of their trace element distribution patterns in the primitive mantle-normalized diagram.One is island arc basalts (lAB),showing enrichment in LILE,Pb and LREE but depletion in HFSE such as Nb and Ta relative to HREE.The other is ocean island basalts (OIB),exhibiting enrichment in LILE and LREE,enrichment or non-depletion in HFSE but depletion in Pb relative to HREE.In either types,these basalts show the enhanced enrichment of LILE and LREE with increasing their incompatibility relative to normal mid-ocean ridge basalts (MORB).The thermal regime of subduction zones can be categorized into two stages in both time and space.The first stage is characterized by compressional tectonism at low thermal gradients.As a consequence,metamorphic dehydration of the subducting crust prevails at forearc to subarc depths due to the breakdown of hydrous minerals such as mica and amphibole in the stability field of garnet and rutile,resulting in the liberation of aqueous solutions with the trace element composition that is considerably enriched in LILE,Pb and LREE but depleted in HFSE and HREE relative to normal MORB.This provides the crustal signature for the mantle sources of IAB.The second stage is indicated by extensional tectonism at high thermal gradients,leading to the partial melting of metamorphically dehydrated crustal rocks at subarc to postarc depths.This involves not only the breakdown of hydrous minerals such as amphibole,phengite and allanite in the stability field of garnet but also the dissolution of futile into hydrous melts.As such,the hydrous melts can acquire the trace element composition that is significantly enriched in LILE,HFSE and LREE but depleted in Pb and HREE relative to normal MORB,providing the crustal signature for the mantle sources of OIB.In either case,these liquid phases would metasomatize the overlying mantle wedge peridotite at different depths,generating ultramafic metasomatites such as serpentinized and chloritized peridotites,and olivine-poor pyroxenites and hornblendites.As a consequence,the crustal signatures are transferred by the liquid phases from the subducting slab into the mantle.
机译:汇聚板块边界的地壳再循环对于地幔非均质性至关重要,但是俯冲带以上玄武岩地幔源中的地壳特征主要是以液相而不是固相的形式结合的。液相的物理化学性质取决于脱水俯冲通道中板-幔界面处地壳岩石的行为。由于不相容微量元素的显着分馏,但放射性同位素相对于地壳源的充分继承,液相的产生对于俯冲带地球化学转移至关重要在这个过程中,俯冲地壳岩石中特定矿物的稳定性对液相中给定微量元素的富集起着主要控制作用。因此,地球化学富集的玄武岩可以分为两种类型原始元素的痕量元素分布模式地幔归一化图。一个是岛弧玄武岩(lAB),显示了LILE,Pb和LREE的富集,但相对于HREE却富集了Nb和Ta等HFSE;另一个是海洋岛玄武岩(OIB),显示了LILE和相对于HREE,HFSE中的LREE,富集或非贫化,但Pb贫化。在这两种类型中,这些玄武岩均表现出LILE和LREE的富集增强,相对于正常的洋中脊玄武岩(MORB)而言增加了不相容性。俯冲带在时间和空间上都可以分为两个阶段。第一阶段的特征是低热梯度下的压缩构造作用。因此,由于含水层的破裂,俯冲地壳的变质脱水普遍存在于前弧至亚弧深度。石榴石和金红石稳定领域中的云母和闪石等矿物,导致水溶液中的微量元素组成大量富集了LILE,Pb和LREE但相对于普通MORB而言,其HFSE和HREE减少了这不仅涉及石榴石稳定性场中含水闪石,闪石,方钠石和尿囊石的分解,而且还涉及将无用物溶解到含水熔体中。因此,含水熔体可以获得富含微量元素的成分。 LILE,HFSE和LREE中的Pb和HREE相对于普通MORB都减少了,这为OIB的地幔源提供了地壳特征。在任何情况下,这些液相都会使上覆的地幔楔形橄榄岩在不同深度发生交变作用,从而生成超镁铁变质岩。蛇纹石和氯化橄榄石,以及橄榄石贫乏的辉石岩和角闪石。液相将液体从俯冲板转移到地幔中。

著录项

  • 来源
    《地学前缘(英文版)》 |2019年第4期|1223-1254|共32页
  • 作者

    Yong-Fei Zheng;

  • 作者单位

    CAS Key Laboratory of Crust-Mantle Materials and Environments, School of Earth and Space Sciences, University of Science and Technology of China, Hefei 230026, China;

  • 收录信息 中国科学引文数据库(CSCD);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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  • 入库时间 2022-08-19 04:29:18
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