{"title":"非克拉通玄武岩型橄榄岩包体中高亲铁元素和187Os特征:揭示太古宙后岩石圈地幔的起源和演化","authors":"A. Luguet, L. Reisberg","doi":"10.2138/RMG.2016.81.06","DOIUrl":null,"url":null,"abstract":"The highly siderophile elements (HSE) consist of the Platinum Group Elements (PGE: Ru, Rh, Pd, Os, Ir, Pt) along with rhenium and gold. These transition elements show relative chemical inertness and high market values, which respectively earned them the additional names of noble metals and precious metals. The HSE show a very pronounced affinity for iron metal, which translates into metal/silicate partition coefficients similar to or higher than 10,000 over large ranges of both pressure and temperature (e.g., O’Neill et al. 1995; Borisov and Palme 2000; Ertel et al. 1999, 2001, 2006, 2008; Fortenfant et al. 2003, 2006; Brenan et al. 2005; Cottrell and Walker 2006; Brenan and McDonough 2009; Laurenz et al. 2010; Mann et al. 2012; see Brenan et al. 2016, this volume for detailed review). Consequently, the HSE are thought to have been efficiently sequestered within the metallic core of our planet during the metal–silicate differentiation of Earth, leaving the silicate counterpart almost HSE-barren. Investigations of mantle peridotites since the 1970s revealed ng.g−1 level abundances as well as close-to-chondritic proportions of the HSE (Chou 1978; Jagoutz et al. 1979; Mitchell and Keays 1981; McDonough and Sun 1995; Becker et al. 2006; Fischer-Godde et al. 2011). Such abundances and inter-HSE fractionations are not predicted for the silicate Earth left after separation of the metallic core for low- or high-pressure core–mantle differentiation (see Brenan et al. 2016, this volume). The close agreement between the osmium isotopic compositions of fertile mantle peridotites and those of chondritic meteorites (Walker et al. 2002a), which requires nearly identical Re/Os ratios in these two reservoirs, provides particularly convincing evidence that the mantle’s HSE content cannot simply represent the residue left after core formation. …","PeriodicalId":49624,"journal":{"name":"Reviews in Mineralogy & Geochemistry","volume":"27 1","pages":"305-367"},"PeriodicalIF":0.0000,"publicationDate":"2016-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"61","resultStr":"{\"title\":\"Highly Siderophile Element and 187Os Signatures in Non-cratonic Basalt-hosted Peridotite Xenoliths: Unravelling the Origin and Evolution of the Post-Archean Lithospheric Mantle\",\"authors\":\"A. Luguet, L. 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Consequently, the HSE are thought to have been efficiently sequestered within the metallic core of our planet during the metal–silicate differentiation of Earth, leaving the silicate counterpart almost HSE-barren. Investigations of mantle peridotites since the 1970s revealed ng.g−1 level abundances as well as close-to-chondritic proportions of the HSE (Chou 1978; Jagoutz et al. 1979; Mitchell and Keays 1981; McDonough and Sun 1995; Becker et al. 2006; Fischer-Godde et al. 2011). Such abundances and inter-HSE fractionations are not predicted for the silicate Earth left after separation of the metallic core for low- or high-pressure core–mantle differentiation (see Brenan et al. 2016, this volume). The close agreement between the osmium isotopic compositions of fertile mantle peridotites and those of chondritic meteorites (Walker et al. 2002a), which requires nearly identical Re/Os ratios in these two reservoirs, provides particularly convincing evidence that the mantle’s HSE content cannot simply represent the residue left after core formation. …\",\"PeriodicalId\":49624,\"journal\":{\"name\":\"Reviews in Mineralogy & Geochemistry\",\"volume\":\"27 1\",\"pages\":\"305-367\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"61\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Reviews in Mineralogy & Geochemistry\",\"FirstCategoryId\":\"89\",\"ListUrlMain\":\"https://doi.org/10.2138/RMG.2016.81.06\",\"RegionNum\":1,\"RegionCategory\":\"地球科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"Earth and Planetary Sciences\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reviews in Mineralogy & Geochemistry","FirstCategoryId":"89","ListUrlMain":"https://doi.org/10.2138/RMG.2016.81.06","RegionNum":1,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Earth and Planetary Sciences","Score":null,"Total":0}
引用次数: 61
摘要
高亲铁元素(HSE)由铂族元素(PGE: Ru, Rh, Pd, Os, Ir, Pt)以及铼和金组成。这些过渡元素具有相对的化学惰性和较高的市场价值,分别被称为贵金属和贵金属。HSE对铁金属表现出非常明显的亲和力,在很大的压力和温度范围内,金属/硅酸盐分割系数接近或高于10,000(例如,O 'Neill等人,1995;鲍里索夫和帕尔梅2000;Ertel等,1999,2001,2006,2008;Fortenfant等人,2003,2006;Brenan et al. 2005;Cottrell and Walker 2006;Brenan and McDonough 2009;Laurenz et al. 2010;Mann et al. 2012;参见Brenan et al. 2016,本卷详细审查)。因此,在地球的金属硅酸盐分化过程中,HSE被认为有效地隔离在地球的金属核心中,使得硅酸盐对应的HSE几乎是贫瘠的。自20世纪70年代以来对地幔橄榄岩的研究表明。g−1水平丰度以及HSE的接近线粒体比例(Chou 1978;Jagoutz et al. 1979;Mitchell and Keays 1981;McDonough and Sun 1995;Becker et al. 2006;fisher - godde et al. 2011)。对于低或高压核幔分异过程中金属岩心分离后留下的硅酸盐土,无法预测这种丰度和hse间分异(见Brenan etal . 2016,本卷)。沃土橄榄岩的锇同位素组成与球粒陨石的锇同位素组成非常接近(Walker et al. 2002a),这要求这两个储层的Re/Os比率几乎相同,这提供了特别有说服力的证据,表明地幔的HSE含量不能简单地代表岩心形成后留下的残留物。…
Highly Siderophile Element and 187Os Signatures in Non-cratonic Basalt-hosted Peridotite Xenoliths: Unravelling the Origin and Evolution of the Post-Archean Lithospheric Mantle
The highly siderophile elements (HSE) consist of the Platinum Group Elements (PGE: Ru, Rh, Pd, Os, Ir, Pt) along with rhenium and gold. These transition elements show relative chemical inertness and high market values, which respectively earned them the additional names of noble metals and precious metals. The HSE show a very pronounced affinity for iron metal, which translates into metal/silicate partition coefficients similar to or higher than 10,000 over large ranges of both pressure and temperature (e.g., O’Neill et al. 1995; Borisov and Palme 2000; Ertel et al. 1999, 2001, 2006, 2008; Fortenfant et al. 2003, 2006; Brenan et al. 2005; Cottrell and Walker 2006; Brenan and McDonough 2009; Laurenz et al. 2010; Mann et al. 2012; see Brenan et al. 2016, this volume for detailed review). Consequently, the HSE are thought to have been efficiently sequestered within the metallic core of our planet during the metal–silicate differentiation of Earth, leaving the silicate counterpart almost HSE-barren. Investigations of mantle peridotites since the 1970s revealed ng.g−1 level abundances as well as close-to-chondritic proportions of the HSE (Chou 1978; Jagoutz et al. 1979; Mitchell and Keays 1981; McDonough and Sun 1995; Becker et al. 2006; Fischer-Godde et al. 2011). Such abundances and inter-HSE fractionations are not predicted for the silicate Earth left after separation of the metallic core for low- or high-pressure core–mantle differentiation (see Brenan et al. 2016, this volume). The close agreement between the osmium isotopic compositions of fertile mantle peridotites and those of chondritic meteorites (Walker et al. 2002a), which requires nearly identical Re/Os ratios in these two reservoirs, provides particularly convincing evidence that the mantle’s HSE content cannot simply represent the residue left after core formation. …
期刊介绍:
RiMG is a series of multi-authored, soft-bound volumes containing concise reviews of the literature and advances in theoretical and/or applied mineralogy, crystallography, petrology, and geochemistry. The content of each volume consists of fully developed text which can be used for self-study, research, or as a text-book for graduate-level courses. RiMG volumes are typically produced in conjunction with a short course but can also be published without a short course. The series is jointly published by the Mineralogical Society of America (MSA) and the Geochemical Society.