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1.
蛇纹岩对地球深部和浅部的元素循环以及氧化还原状态调节具有非常重要的作用。蛇纹岩中的流体活动性元素(fluid- mobile element, FME)是揭示地幔岩石水化、脱水以及元素循环的关键。本文系统收集和分析了前人报道的不同构造环境的蛇纹岩矿物化学、全岩微量元素和非传统稳定同位素(Fe、Zn、Cu)的组成特征，试图从多个角度总结蛇纹岩脱水过程的元素迁移规律及流体性质。蛇纹岩主要矿物蛇纹石微量元素含量具有以下主要特征：① 不同变质程度的蛇纹岩中的蛇纹石既包含轻稀土元素(light rare earth element, LREE)富集，又包含LREE亏损的特征；② 纤蛇纹石的REE和微量元素分布在利蛇纹石和叶蛇纹石的范围内，利蛇纹石重稀土元素(heavy rare earth element, HREE)整体上略高于叶蛇纹石且更加富集FME；③ 通过中度不相容元素与REE含量相结合，能够较好地区分橄榄石和辉石蛇纹石化所形成的蛇纹石，即辉石形成的蛇纹石富集相容元素(如Sc、Zn、Cr、Y和Ti等)并具有较高的HREE，而橄榄石形成的蛇纹石则表现为平坦且整体较低的REE分布型式。在蛇纹岩全岩微量元素和稀土元素(rare earth element, REE)含量方面，不同构造环境的蛇纹岩具有较大范围的重叠，但也有一定的差异：① 慢速扩张的印度洋中脊蛇纹岩REE和微量元素含量要整体高于快速扩张的大西洋中脊和太平洋中脊的蛇纹岩；② 马里亚纳蛇纹岩泥相比于蛇纹岩和蛇纹石化纯橄岩具有更高的REE和微量元素，而蛇纹石化纯橄岩相比于蛇纹岩则具有相对低的REE及流体不活动性元素含量。因此，利用微量元素的含量在区分不同环境的蛇纹岩方面存在一定的困难。但是，碱金属元素与U元素含量及其相应的比值，则可以较明显区分出大洋蛇纹岩和弧前蛇纹岩。目前已发表的蛇纹岩Fe、Zn、Cu同位素数据表明：① 蛇绿岩中的蛇纹岩Fe和Zn同位素的分馏与其变质程度密切相关。蛇纹岩在进变质过程中δ 56Fe值与Fe 3+/∑Fe值呈负相关，而Zn含量和δ 66Zn值则呈现正相关，表明蛇纹岩变质脱水能够释放氧化性流体；② 与橄榄岩相比，蛇纹岩具有明显低的δ 65Cu值，表明橄榄岩蛇纹石化过程中存在氧化性流体的加入。蛇纹岩Fe、Zn、Cu同位素在示踪流体性质和氧化还原状态方面有很大潜力，对壳幔系统的化学循环具有重要意义。 相似文献
2.
陈伊翔 《矿物岩石地球化学通报》2021,40(5):1034-1048
蛇纹岩在俯冲带地球化学循环中发挥着重要作用.蛇纹岩是俯冲带中极富Mg和Fe的矿物,其变质脱水释放的流体含有显著量的Mg和Fe,对俯冲带中Mg、Fe元素的循环及其同位素的分馏行为起着重要作用.蛇纹岩脱水过程中的Mg、Fe同位素分馏特征与不同温度、压力条件下蛇纹岩体系的矿物组合、释放流体的氧化还原状态、流体中Mg、Fe的价态和种型等密切相关.本文在总结俯冲带蛇纹岩的产出特征、稳定性和主要脱水反应的基础上,系统评述了俯冲带蛇纹岩在变质脱水过程中Mg、Fe同位素分馏行为的研究现状和存在的关键科学问题,并对未来的研究方向进行了展望. 相似文献
3.
俯冲带蛇纹岩的变质过程 总被引：3，自引：1，他引：2
俯冲带蛇纹岩是俯冲带流体的重要来源,特别是其深部脱水作用对地幔动力学影响深远,是研究俯冲带约80~200km深度范围的地球动力学的关键,因此研究蛇纹岩的变质作用过程及其相关特征矿物(组合)的温压稳定范围具有重要意义。蛇纹岩具有简单的矿物(组合):蛇纹石类、硅镁石类、磁铁矿、氢氧镁石、绿泥石、橄榄石、透辉石、角闪石、滑石等,并且这些矿物(组合)对温压变化不敏感从而很难用来判定蛇纹岩所经历的变质演化轨迹。近几十年来,研究者通过实验岩石学和野外地质观察,主要研究了蛇纹石类矿物和硅镁石类矿物的温压稳定范围,并且试图使用这些特征矿物(组合)来判定俯冲带蛇纹岩的峰期变质条件。本文总结了蛇纹岩中这些主要矿物的温压稳定范围和相关变质反应,并且以中国西南天山蛇纹岩为例,展示使用特征矿物(组合)和叶蛇纹石Al等值线判定蛇纹岩峰期温压条件在实际岩石中的应用。另外,早期对叶蛇纹石的研究表明:随着温压条件的变化,叶蛇纹石的晶体结构会发生相应的调整。表现为单位晶胞内硅氧四面体的个数(m值)发生变化:温度升高,m值变小;压力升高,m值变大,这个发现在高压实验和天然样品中得到了一定程度的验证。本文利用已知峰期温压范围的叶蛇纹石样品分别采用粉末制样法和离子减薄制样法,进行透射电镜测试(TEM)样品的m值,并通过统计的方法获得叶蛇纹石的m值的峰值。结果显示叶蛇纹石的m值的峰值在一定程度上可以用以指示温压条件。本文提出可以用矿物组合、叶蛇纹石Al等值线和叶蛇纹石m值峰值相结合的方法确定蛇纹岩的变质温压条件和P-T轨迹。 相似文献
4.
基性和超基性岩蛇纹石化的机理及成矿潜力 总被引：4，自引：3，他引：1
蛇纹石化是指基性岩（例如玄武岩）和超基性岩（橄榄岩、科马提岩等）在中、低温条件下产生的含蛇纹石的水热蚀变。蛇纹石化可以出现在不同的地质构造环境中,例如大洋底、扩张洋脊和俯冲带。蛇纹石化的特别之处在于：蛇纹石化过程中产生氢气,这可能解释地球早期生命起源的问题;蛇纹石化生成磁铁矿;蛇纹石富水（可达13%）;蛇纹石富Cl、Li、Sr、As等元素。蛇纹石在高温下（>700℃）脱水形成橄榄石,Li、Sr、As等元素富集在流体中,流体交代地幔楔可改变地幔的微量元素组成。此外,铁矿、金矿和银矿等可赋存于蛇纹岩中,矿床的形成可能和基性或超基性岩的蛇纹石化相关。本文从以下4个方面探讨蛇纹石化的机理：（1）蛇纹石化的产物,主要介绍和蛇纹石化相关的热液流体的组成,蛇纹石化过程中产生氢气的量,利蛇纹石、纤蛇纹石和叶蛇纹石的形成条件,水镁石的形成条件,以及磁铁矿的形成;（2）蛇纹石化的反应速率;（3）蛇纹石化过程中元素的迁移;（4）蛇纹石化的成矿潜力。 相似文献
5.
蛇纹石化是海底最重要的水岩相互作用之一,指基性岩和超基性岩中的橄榄石和辉石等镁铁质矿物在相对低温条件下发生水热蚀变产生蛇纹石等矿物的热液变质作用。蛇纹石族矿物主要有三种,分别是利蛇纹石、纤蛇纹石和叶蛇纹石。低温状态蛇纹石族矿物主要以利蛇纹石和纤蛇纹石的形式存在,高温状态下主要以叶蛇纹石的形式存在。影响大洋蛇纹石化过程的因素不容忽视,温度、氧化还原程度、pH值、水岩比(W/R)等都在其中扮演着重要的角色。总的来说,地幔物质易出露在地壳减薄区域和断裂构造处,这有利于与流体充分接触反应,从而决定了大洋蛇纹石化作用发生的可能位置。对蛇纹石化程度的描述,当前人们大多通过岩石微观结构、地球化学指标来定性指示,磁学指标有望实现对蛇纹石化程度的定量解释。蛇纹石化作用对海底磁异常、地球生命演化进程、成矿作用等都有一定的贡献。此外,俯冲带脱水及弧岩浆的形成都与之有联系。总之,基性与超基性岩石蛇纹石化与俯冲带蛇纹岩脱水过程是地球水循环过程的重要机制,但未来揭示蛇纹岩的磁学性质和俯冲变质过程,仍需进一步探索。 相似文献
6.
俯冲洋壳的脱水作用对于岛弧火山岩的成因具有重要意义。西天山高压低温变质带中切割主岩蓝片岩/榴辉岩的榴辉岩相脉体记录了古生代俯冲带中的脱水过程。脉体具有典型高压矿物组合：石榴石(＞8%)+绿辉石(15%)+石英(＞55%)+蓝闪石(5%)+冻蓝闪石(10%)±黝帘石±方解石。高压脉及其主岩的岩相学与矿物化学研究表明流体是在俯冲过程中蓝片岩向榴辉岩进变质条件下释放。脉的主量元素成分显示流体富Si。主岩的稀土元素和微量元素表明其原岩为洋岛玄武岩(OIB)。脉和主岩具有相似的微量元素配分模式,并且相对N-MORB都显示富Li、Be、Cs、Rb、Ba、Pb、La的特点。通过模拟计算,在高压脉、与脉平衡的流体以及模拟的原生流体中都富集流体活动性元素(Li、Be、Pb)和LILE(Cs、Rb、Ba),贫HFSE(Nb)和REE(Nd、Sm)。证实了在古生代南天山洋俯冲时洋岛玄武岩脱水释放出富Li、Be、LILE、La和Pb,贫HFSE和HREE的流体。 相似文献
7.
关于造山带幔源橄榄岩变质演化的一个普遍规律? 总被引：1，自引：1，他引：0
来自柴达木盆地北缘、西藏雅鲁藏布江和苏鲁等三个造山带的橄榄岩样品中均存在蛇纹岩矿物被包裹于橄榄岩矿物的现象.包裹体矿物包括利蛇纹石、纤维蛇纹石、叶蛇纹石、磁铁矿、水镁石、斜方和单斜角闪石、绿泥石、滑石、Fe-Ni硫化物、含水钙铬榴石、钙铝榴石、脆云母等,它们指示橄榄岩先从地幔就位于地壳发生蛇纹岩化再经历高压变质作用的过程,记录着岩石圈从裂解到碰撞的演化历史.结合近来国际上出现的类似报道,本文提出这是造山带变质橄榄岩的一个普遍规律.因此,造山带变质橄榄岩的化学组成不同程度地受到地壳物质的混染,不能准确反映原始上地幔的组成. 相似文献
8.
在板片俯冲过程中,基性洋壳、下伏蛇纹石化岩石圈地幔和覆盖在俯冲洋壳上的大洋沉积物在不同深度会依次发生板片脱水作用和沉积物熔融,形成的俯冲带熔/流体可携带某些元素交代地幔楔,进而通过弧岩浆作用返回地壳。同时,俯冲板片内不同组分之间也会发生化学成分的迁移和交换,并最终进入深部地幔,造成地幔不均一性和不同程度壳幔相互作用。本文报道了我国西南天山典型高压-超高压变质带中蛇纹岩、辉石岩、绿片岩、蓝片岩和榴辉岩内各矿物相的主量元素及Cu、Co、Ni含量数据。结果表明,除辉石岩中透辉石的Cu含量较高(1.26×10-6～76.9×10-6)外,其它硅酸盐矿物的Cu含量均在1.0×10-6～10.0×10-6左右;而Co和Ni在不同岩性及不同矿物之间显示较大的含量差异：蛇纹岩中蛇纹石的Co和Ni含量分别为22.6×10-6～49.6×10-6和482×10-6～1097×10-6,榴辉岩中绿辉石的Co和Ni含量分别为6.0×10... 相似文献
9.
青海茫崖石棉矿区超基性岩体是由原岩以纯橄岩、辉橄岩和橄辉岩为主体组成的富镁质超基性岩体,经历自变质和后期多期热液的叠加变质蚀变作用,经蛇纹石化后形成蚀变完全的蛇纹岩岩体,其中部分蛇纹岩又进一步发生滑石化及碳酸盐化蚀变为滑石菱镁片岩、菱镁滑石片岩、滑石片岩和菱镁岩等。本文在野外地质调查基础上,在室内通过镜下岩矿综合鉴定、全岩化学成分分析以及电子探针成分分析等手段进行了岩石化学特征、矿物学特征及其蚀变演化过程研究。结果表明,该变质超基性岩体蛇纹岩主要特征组合矿物为蛇纹石(利蛇纹石、叶蛇纹石、纤蛇纹石)、磁铁矿、菱镁矿、滑石、水镁石、铬铁矿,变余矿物有斜方辉石、单斜辉石和铬铁矿,滑石菱镁片岩类主要组成矿物为菱镁矿、滑石、蛇纹石及磁铁矿,局部可见石英脉。该地区变质超基性岩体较完整地记录了橄榄岩水化、滑石化及碳酸盐化作用过程的各个阶段,超基性岩蚀变演化过程主要有两个作用阶段:(Ⅰ)橄榄石、辉石类矿物的蛇纹石化作用及蛇纹石绿泥石化作用;(Ⅱ)富Ca、CO2流体交代蛇纹石、滑石及水镁石的碳酸盐化作用。蛇纹石化等变质蚀变作用促进了Si、Mg及Fe元素化学活动性,使元素发生富集与迁移,对于次生矿物的形成与演化起到了一定的催化作用。多期不同组成流体热液的交代作用过程,清晰地展示了利蛇纹石、纤蛇纹石和叶蛇纹石的演化序列,以及滑石、水镁石、铬铁矿和磁铁矿的形成过程及标形特征。 相似文献
10.
硼的地球化学性质及其在俯冲带的循环与成矿初探 总被引：2，自引：1，他引：1
硼是广泛应用于化工、农业、材料科学及核工业领域的重要元素。硼与氢的核聚变反应是未来具备运用潜力的清洁能源。硼作为典型的亲石元素,是高度不相容元素。硼元素容易富集于蚀变洋壳及蛇纹石化地幔橄榄岩中。而在板块俯冲过程中,由于硼具有强的流体活动性,会优先赋存于流体中。因此,当蛇纹石化的大洋岩石圈及覆于其上的沉积物在俯冲过程中发生脱水,这使得弧前地幔楔发生大规模的蛇纹石化。此时大量硼元素很可能随俯冲流体释放并封存于弧前地幔楔中。目前已发现的超大型硼矿床主要位于聚合型板块边缘,尤其土耳其拥有世界上最大的硼酸盐储量。我们推测这些矿床的形成基础条件之一可能与弧前高度蛇纹石化的地幔楔有关。尤其是在洋 陆俯冲环境,弧前蛇纹岩或蛇绿混杂岩首先通过俯冲侵蚀再循环到火山弧岩浆中,使得岩浆更富集硼。随后弧火山喷发大量富硼的火山岩、岩浆热液及水气。在岩浆冷却过程中,硼元素析出、沉淀于火山表面,并伴随风化、侵蚀过程汇聚至碰撞造山带的封闭湖盆之中。此外,干冷的气候条件下也进一步促进了硼的成矿。我国具有形成大型、超大型硼矿的地质条件,应加大研究及探勘力度,并适当购买硼作为战略储备。 相似文献
11.
The Totalp-Platta-Malenco ophiolites in the Eastern Central Alps offer a unique opportunity to study the behaviour of Li, Be and B in ultramafic rocks in response to serpentinization and to progressive Alpine metamorphism. These units represent the remnants of a former ocean-continent transition that was intensely serpentinized during exposure on the Jurassic seafloor of the Ligurian Tethys. From north to the south, three isograd reactions (lizardite⇒antigorite+brucite;lizardite+talc⇒antigorite;lizardite+tremolite⇒antigorite+diopside) have been used to quantify the evolution of the light element content of metamorphic minerals. We determined the Li, Be and B concentrations in major silicate minerals from the ultramafic bodies of Totalp, Platta and Malenco by secondary ion mass spectrometry. Mantle minerals have Be concentrations (e.g. <0.001-0.009 μg/g in olivine) similar to the metamorphic minerals that replace them (e.g. <0.001-0.016 μg/g in serpentine). The mantle signature of Be is thus neither erased during seafloor alteration nor by progressive metamorphism from prehnite-pumpellyite to epidote-amphibolite facies. In contrast, the Li and B inventories of metamorphic minerals are related to the lizardite-to-antigorite transition. Both elements display higher concentrations in the low-temperature serpentine polymorph lizardite (max. 156 μg/g Li, max. 318 μg/g B) than in antigorite (max. 0.11 μg/g Li, max. 12 μg/g B). Calculated average B/Li ratios for lizardite (∼1395) and antigorite (∼115) indicate that Li fractionates from B during the lizardite-to-antigorite transition during prograde metamorphism in ultramafic rocks. In subduction zones, this signature is likely to be recorded in the B-rich nature of forearc fluids.Relative to oceanic mantle the Be content of mantle clinopyroxene is much higher, but similar to Be values from mantle xenoliths and subduction-related peridotite massifs. These data support previous hypothesis that the mantle rocks from the Eastern Central Alps have a subcontinental origin. We conclude that Be behaves conservatively during subduction metamorphism of ultramafic rocks, at least at low-temperature, and thus retains the fingerprint of ancient subduction-related igneous events in mantle peridotites. 相似文献
12.
Fabien Deschamps Stéphane Guillot Marguerite Godard Catherine Chauvel Muriel Andreani Kéiko Hattori 《Chemical Geology》2010,269(3-4):262-277
The Tso Morari serpentinites in the Ladakh area, northwest Himalaya, originated from the forearc mantle overlying the northward subducting Neo-Tethys lithosphere and the margin of the Indian continent. The serpentinites are characterized by high concentration of fluid-mobile elements (FME: As, Sb, B, Li, and U) compared to ophiolitic or abyssal serpentinites. The Pb isotopic compositions of serpentinites show influence of the subducted Indian continental lithosphere. Trace element concentrations of antigorite determined in situ with Laser Ablation High Resolution Inductively Coupled Mass Spectrometer (LA-HR-ICP-MS) show high contents of FME including Pb, in contrast to the spatially associated iron oxides. Rare earth elements (REE) and compatible elements, such as Sc and Co, remained immobile during the hydration, allowing the identification of the primary minerals (olivine or orthopyroxene) from which serpentine formed. Serpentinized olivine displays higher Sb and As concentrations (up to 1000 × PM) than serpentinized orthopyroxenes that are enriched in Pb, Cs and Li (2 to up to 10 × PM).We propose that the observed FME distribution in two types of serpentine reflect the differential incorporation of FME during the downward movement of the serpentinite along the subduction plane. At temperature lower than 400 °C, at shallow depths, olivine is preferentially serpentinized and incorporates elements that are fluid soluble at low temperatures, such as Sb and As. Above 400 °C, orthopyroxene is hydrated and incorporates Pb, Cs, Li and possibly Ba. Boron and U are incorporated in both types of serpentine suggesting that they are released from slabs at temperatures around 300–400 °C. The serpentine acts as a sink for water, but also for FME and transports them to deeper and hotter levels in the mantle, down to the isotherm 600–650 °C where dehydration occurs. 相似文献
13.
J. Cárdenas-Párraga A. García-Casco J. A. Proenza G. E. Harlow I. F. Blanco-Quintero C. Lázaro 《International Geology Review》2017,59(16):2041-2064
The Sierra del Convento and La Corea mélanges (eastern Cuba) are vestiges of a Cretaceous subduction channel in the Caribbean realm. Both mélanges contain blocks of oceanic crust and serpentinite subducted to high pressure within a serpentinite matrix. The bulk composition of serpentinite indicates spinel-harzburgite and -herzolite protoliths. The samples preserve fertile protolith signatures that suggest low melting degrees. High concentration of immobile elements Zr, Th, Nb, and REE contents (from ~0.1 to ~2 CI-chondrite) point to early melt–rock interaction processes before serpentinization took place. Major- and trace-element compositions suggest an oceanic fracture-zone–transform-fault setting. A mild negative Eu anomaly in most samples indicates low-temperature fluid–rock interaction as a likely consequence of seawater infiltration during oceanic serpentinization. A second, more important, serpentinization stage is related to enrichment in U, Pb, Cs, Ba, and Sr due to the infiltration of slab-derived fluids. The mineral assemblages are mainly formed by antigorite, lizardite, and chlorite, with local minor talc, tremolite, anthophyllite, dolomite, brucite, and relict orthopyroxene. The local presence of anthophyllite and the replacements of lizardite by antigorite indicate a metamorphic evolution from the cooling of peridotite/serpentinite at the oceanic context to mild heating and compression in a subduction setting. We propose that serpentinites formed at an oceanic transform-fault setting that was the locus of subduction initiation of the Proto-Caribbean basin below the Caribbean plate during early Cretaceous times. Onset of subduction at the fracture zone allowed the preservation of abyssal transform-fault serpentinites at the upper plate, whereas limited downward drag during mature subduction placed the rocks in the subduction channel where they tectonically mixed with the upward-migrating accreted block of the subducted Proto-Caribbean oceanic crust. Hence, we suggest that relatively fertile serpentinites of high-pressure mélanges were witness to the onset of subduction at an oceanic transform-fault setting. 相似文献
14.
The effect of chrysotile nanotubes on the serpentine-fluid Li-isotopic fractionation 总被引：1，自引：0，他引：1
Bernd Wunder Fabien Deschamps Anke Watenphul Stéphane Guillot Anette Meixner Rolf L. Romer Richard Wirth 《Contributions to Mineralogy and Petrology》2010,159(6):781-790
We determined the lithium isotope fractionation between synthetic Li-bearing serpentine phases lizardite, chrysotile, antigorite,
and aqueous fluid in the P,T range 0.2–4.0 GPa, 200–500°C. For experiments in the systems lizardite-fluid and antigorite-fluid, 7Li preferentially partitioned into the fluid and Δ7Li values followed the T-dependent fractionation of Li-bearing mica-fluid (Wunder et al. 2007). By contrast, for chrysotile-fluid experiments, 7Li weakly partitioned into chrysotile. This contrasting behavior might be due to different Li environments in the three serpentine
varieties: in lizardite and antigorite lithium is sixfold coordinated, whereas in chrysotile lithium is incorporated in two
ways, octahedrally and as Li-bearing water cluster filling the nanotube cores. Low-temperature IR spectroscopic measurements
of chrysotile showed significant amounts of water, whose freezing point was suppressed due to the Li contents and the confined
geometry of the fluid within the tubes. The small inverse Li-isotopic fractionation for chrysotile-fluid results from intra-crystalline
Li isotope fractionation of octahedral Li[6] with preference to 6Li and lithium within the channels (Li[Ch]) of chrysotile, favoring 7Li. The nanotubes of chrysotile possibly serve as important carrier of Li and perhaps also of other fluid-mobile elements
in serpentinized oceanic crust. This might explain higher Li abundances for low-T chrysotile-bearing serpentinites relative to high-T serpentinites. Isotopically heavy Li-bearing fluids of chrysotile nanotubes could be released at relatively shallow depths
during subduction, prior to complete chrysotile reactions to form antigorite. During further subduction, fluids produced during
breakdown of serpentine phases will be depleted in 7Li. This behavior might explain some of the Li-isotopic heterogeneities observed for serpentinized peridotites. 相似文献
15.
西藏班公湖-怒江缝合带中西段康穷蛇纹岩的岩石学、地球化学特征及其构造意义 总被引：2，自引：0，他引：2
康穷蛇纹岩出露于班公湖-怒江缝合带的中西段,是康穷蛇绿混杂岩的超基性岩石端元。依据全岩地球化学元素含量,可将康穷蛇纹岩划分为A组和B组2种。两者均富集大离子亲石元素(Rb、Cs)和高场强元素(U、Nb)。经估算,A组蛇纹岩原岩是原始地幔经过10%~17%部分熔融的地幔残留,B组蛇纹岩原岩经历过更高程度的部分熔融(17%~23%),表明康穷蛇纹岩原岩至少经历过两阶段的部分熔融。初步研究认为,A组蛇纹岩原岩是洋内俯冲初始阶段上涌软流圈地幔部分熔融的地幔残留,受类MOR型熔体交代作用而仍然亏损轻稀土元素(LREE),却富集U和Nb,属类MOR型地幔橄榄岩;B组蛇纹岩原岩是A组蛇纹岩原岩在洋内俯冲带环境再熔融的产物,受玻安质熔体交代作用而相对富集轻稀土元素,属弧前地幔橄榄岩。两者均发生蛇纹石化作用而转变成蛇纹岩,最终因大洋碰撞闭合而残存于缝合带内,是班公湖-怒江新特提斯洋洋内俯冲演化阶段的岩石记录。 相似文献
16.
Baptiste Debret Kenneth T. Koga Christian Nicollet Muriel Andreani Stéphane Schwartz 《地学学报》2014,26(2):96-101
The abundances of F, Cl and S in arc magmas are systematically higher than in other mantle‐derived magmas, suggesting that these elements are added from the slab along with H2O. We present ion probe microanalyses of F, Cl and S in serpentine minerals that represent the P–T evolution of the oceanic lithosphere, from its serpentinization at the ridge, to its dehydration at around 100 km depth during subduction. F, Cl and S are incorporated early into serpentine during its formation at mid‐ocean ridges, and serpentinized lithosphere then carries these elements to subduction zones. More than 50% of the F, Cl and S are removed from serpentine during the prograde metamorphic lizardite/antigorite transition. Due to the low solubility of F in water, and to the low amount of water released during this phase transition, the fluids mobilizing these elements must be dominated by SOX rather than H2O. 相似文献
17.
B. DEBRET C. NICOLLET M. ANDREANI S. SCHWARTZ M. GODARD 《Journal of Metamorphic Geology》2013,31(2):165-186
The Lanzo peridotite massif is a fragment of oceanic lithosphere generated in an ocean–continent transition context and eclogitized during alpine collision. Despite the subduction history, the massif has preserved its sedimentary oceanic cover, suggesting that it may have preserved its oceanic structure. It is an exceptional case for studying the evolution of a fragment of the lithosphere from its oceanization to its subduction and then exhumation. We present a field and petrological study retracing the different serpentinization episodes and their impact on the massif structure. The Lanzo massif is composed of slightly serpentinized peridotites (<20% serpentinization) surrounded by an envelope of foliated serpentinites (100% serpentinization) bordered by oceanic metabasalts and metasedimentary rocks. The limit between peridotites and serpentinites defines the front of serpentinization. This limit is sharp: it is marked by the presence of massive serpentinites (80% serpentinization) and, locally, by dykes of metagabbros and mylonitic gabbros. The deformation of these gabbros is contemporaneous with the emplacement of the magma. The presence of early lizardite in the peridotites testifies that serpentinization began during the oceanization, which is confirmed by the presence of meta‐ophicarbonates bordering the foliated serpentinite envelope. Two additional generations of serpentine occur in the ultramafic rocks. The first is a prograde antigorite that partially replaced the lizardite and the relict primary minerals of the peridotite during subduction, indicating that serpentinization is an active process at the ridge and in the subduction zone. Locally, this episode is followed by the deserpentinization of antigorite at peak P–T (estimated in eclogitized metagabbros at 2–2.5 GPa and 550–620 °C): it is marked by the crystallization of secondary olivine associated with chlorite and/or antigorite and of clinopyroxene, amphibole and chlorite assemblages. A second antigorite formed during exhumation partially to completely obliterating previous textures in the massive and foliated serpentinites. Serpentinites are an important component of the oceanic lithosphere generated in slow to ultraslow spreading settings, and in these settings, there is a serpentinization gradient with depth in the upper mantle. The seismic Moho limit could correspond to a serpentinization front affecting the mantle. This partially serpentinized zone constitutes a less competent level where, during subduction and exhumation, deformation and fluid circulation are localized. In this zone, the reaction kinetics are increased and the later steps of serpentinization obliterate the evidence of this progressive zone of serpentinization. In the Lanzo massif, this zone fully recrystallized into serpentinite during alpine subduction and collision. Thus, the serpentinite envelope represents the oceanic crust as defined by geophysicists, and the sharp front of serpentinization corresponds to an eclogitized seismic palaeo‐Moho. 相似文献
18.
Serpentinites in the Eastern Desert (ED) of Egypt represent integral components of the ophiolites. Metamorphic textures of the serpentinites preserve the complex mineralogical evolution from primary peridotite through metamorphism, and late-stage hydrothermal alteration. Two textural types are distinguished in the olivines of the present serpentinized peridotites, namely (a) highly-strained olivine grains with kink bands, as in the deformed mantle tectonites from ophiolites, and (b) non-strained grains. The latter may represent recrystallized crystals during later thermal metamorphic events due to the intrusion of granite. On the basis of X-ray diffraction analysis, antigorite is the main serpentine minerals with lesser chrysotile and lizardite which indicates that serpentinites were formed under prograde metamorphism. Relict primary minerals of the serpentinites are Cr-spinel, olivine and pyroxene. Chrome spinel relicts have high Cr# (0.60–0.80), whereas primary olivines are Mg-rich nature (Fo = 89–96). Geochemical compositions of serpentinites indicate that they formed not at mid-ocean ridges but at spreading centers associated with subduction zones and this could have happened in a supra-subduction zone either in the fore-arc or back-arc environments. Mineral compositions of primary chrome spinels and olivines are similar to those of modern fore-arcs. High Cr# in the relict chrome spinels and Fo in the primary olivines of serpentinites indicate that they are residual after extensive partial melting and originated by sea-floor spreading during subduction initiation. 相似文献
19.
Arman Boskabadi Iain K. Pitcairn Curt Broman Adrian Boyce Damon A. H. Teagle Matthew J. Cooper 《International Geology Review》2017,59(4):391-419
Ultramafic portions of ophiolitic fragments in the Arabian–Nubian Shield (ANS) show pervasive carbonate alteration forming various degrees of carbonated serpentinites and listvenitic rocks. Notwithstanding the extent of the alteration, little is known about the processes that caused it, the source of the CO2 or the conditions of alteration. This study investigates the mineralogy, stable (O, C) and radiogenic (Sr) isotope composition, and geochemistry of suites of variably carbonate altered ultramafics from the Meatiq area of the Central Eastern Desert (CED) of Egypt. The samples investigated include least-altered lizardite (Lz) serpentinites, antigorite (Atg) serpentinites and listvenitic rocks with associated carbonate and quartz veins. The C, O and Sr isotopes of the vein samples cluster between ?8.1‰ and ?6.8‰ for δ13C, +6.4‰ and +10.5‰ for δ18O, and 87Sr/86Sr of 0.7028–0.70344, and plot within the depleted mantle compositional field. The serpentinites isotopic compositions plot on a mixing trend between the depleted-mantle and sedimentary carbonate fields. The carbonate veins contain abundant carbonic (CO2±CH4±N2) and aqueous-carbonic (H2O-NaCl-CO2±CH4±N2) low salinity fluid, with trapping conditions of 270–300°C and 0.7–1.1 kbar. The serpentinites are enriched in Au, As, S and other fluid-mobile elements relative to primitive and depleted mantle. The extensively carbonated Atg-serpentinites contain significantly lower concentrations of these elements than the Lz-serpentinites suggesting that they were depleted during carbonate alteration. Fluid inclusion and stable isotope compositions of Au deposits in the CED are similar to those from the carbonate veins investigated in the study and we suggest that carbonation of ANS ophiolitic rocks due to influx of mantle-derived CO2-bearing fluids caused break down of Au-bearing minerals such as pentlandite, releasing Au and S to the hydrothermal fluids that later formed the Au-deposits. This is the first time that gold has been observed to be remobilized from rocks during the lizardite–antigorite transition. 相似文献
20.
O–H isotope ratios of high pressure ultramafic rocks: implications for fluid sources and mobility in the subducted hydrous mantle 总被引：2，自引：0，他引：2
Gretchen L. Früh-Green Marco Scambelluri Franca Vallis 《Contributions to Mineralogy and Petrology》2001,141(2):145-159
We examine the O-H isotope signatures of Alpine ultramafic rocks and eclogitic metagabbros of the Erro-Tobbio peridotite Unit (western Italian Alps), which record a subduction and exhumation cycle. Localization of subduction-related deformation along serpentinite mylonite shear zones favoured preservation of pre-subduction mantle and low temperature (oceanic) alteration assemblages within undeformed (meta)peridotite that underwent partial static recrystallization to high-pressure metamorphic parageneses. Bulk rock and mineral separate (clinopyroxene and serpentine) oxygen isotope ratios of the serpentinized mantle peridotites (5-8) are slightly enriched in 18O compared with those of the high-pressure metaperidotites and the serpentinite mylonites (4.4-7.6). The lowest values occur in high-pressure veins (3.5-5.7) and eclogitic metagabbros (3.1-5.3). These variations are comparable to variations observed in modern oceanic rocks and in non-subducted ophiolites. Preservation of pre-eclogitic '18O signatures of the Erro-Tobbio rocks and a lack of oxygen isotope re-equilibration between different shear zones imply local-scale fluid flow at low water/rock ratios and closed system behaviour during high-pressure metamorphism. Different serpentine generations show a bimodal distribution in 'D values: pre-eclogitic lizardite and chrysotile range from -102 to -77; high-pressure antigorite in the mylonites and in low strain metaperidotites range from -71 to -57 and -83 to -60, respectively. Comparable ranges occur in antigorite in the associated high-pressure veins, suggesting that the hydrogen signatures were acquired prior to veining. We propose that the isotopic variations reflect multiple events of fluid uptake in different geodynamic environments. The H- and O-isotope ratios in the eclogitic mylonites suggest that initial hydration occurred over a range of temperatures during local interaction with altered seawater along oceanic shear zones. The 18O-enriched and H-depleted compositions of chrysotile and lizardite in the mantle peridotites suggest that a second hydration event may have occurred as a result of interaction with metamorphic fluids at the early stages of burial in a forearc setting, where slabs undergo large-scale, low-temperature fluid fluxing. The oceanic mantle is thus a candidate for continuous hydration during its oceanic and early subduction history. The Erro-Tobbio unit thus represents an example of cycling of internally-derived fluids, whereby the different structural and textural domains behaved as relatively closed systems to fluid circulation during high-pressure metamorphism. 相似文献