Damanveer S. Grewal , Surjyendu Bhattacharjee , Gabriel-Darius Mardaru , Paul D. Asimow
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However, the utility of this proxy is limited by the lack of knowledge of N isotope fractionation during core crystallization. Using high pressure-high temperature experiments, we show that equilibrium N isotopic fractionation between solid and liquid metal (Δ<sup>15</sup>N<sup>solid–liquid</sup> = δ<sup>15</sup>N<sup>solid</sup> − δ<sup>15</sup>N<sup>liquid</sup>) is limited (≤1.2 ‰) under conditions relevant for core crystallization. This, combined with the siderophile character of N and limited equilibrium N isotope fractionation during core-mantle differentiation, suggests that the δ<sup>15</sup>N values of iron meteorites accurately represent the N isotopic composition of their parent bodies. Unlike the variation in the N isotope ratios of NC and CC chondrites, which can be attributed to the effects of parent-body processes acting on organic precursors, the <sup>15</sup>N-poor nature of NC irons relative to CC irons likely offers the most definitive evidence for the distinct N isotopic compositions of the earliest inner and outer solar system planetesimals. The N isotopic composition of Earth’s primordial mantle (δ<sup>15</sup>N = <−40 ‰) suggests that it retains the memory of the early accretion of <sup>15</sup>N-poor NC iron meteorite parent body-like planetesimals. The early accreted <sup>15</sup>N-poor nitrogen may be stored in the deep mantle, segregated into the core, or lost to space during atmospheric loss caused by impacts. This signature was overprinted by the subsequent accretion and admixing of CC materials, which is reflected in the relatively <sup>15</sup>N-rich nature of Earth’s atmosphere (δ<sup>15</sup>N = 0) and convecting mantle (δ<sup>15</sup>N = −5 ‰).</div></div>","PeriodicalId":327,"journal":{"name":"Geochimica et Cosmochimica Acta","volume":"388 ","pages":"Pages 34-47"},"PeriodicalIF":4.5000,"publicationDate":"2024-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Tracing the origin of volatiles on Earth using nitrogen isotope ratios in iron meteorites\",\"authors\":\"Damanveer S. Grewal , Surjyendu Bhattacharjee , Gabriel-Darius Mardaru , Paul D. 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Using high pressure-high temperature experiments, we show that equilibrium N isotopic fractionation between solid and liquid metal (Δ<sup>15</sup>N<sup>solid–liquid</sup> = δ<sup>15</sup>N<sup>solid</sup> − δ<sup>15</sup>N<sup>liquid</sup>) is limited (≤1.2 ‰) under conditions relevant for core crystallization. This, combined with the siderophile character of N and limited equilibrium N isotope fractionation during core-mantle differentiation, suggests that the δ<sup>15</sup>N values of iron meteorites accurately represent the N isotopic composition of their parent bodies. Unlike the variation in the N isotope ratios of NC and CC chondrites, which can be attributed to the effects of parent-body processes acting on organic precursors, the <sup>15</sup>N-poor nature of NC irons relative to CC irons likely offers the most definitive evidence for the distinct N isotopic compositions of the earliest inner and outer solar system planetesimals. 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引用次数: 0
摘要
了解太阳系早期行星胚胎和陆地储层的氮(N)同位素比率之间的关系对于追溯地球上挥发性物质的起源至关重要。地球主要是由内太阳系迅速(CAIs 后 1-2 Ma 内)吸积的类行星和行星胚胎(也称为非碳质(NC)储层)生长而来的。岩浆铁陨石对太阳系最早的类行星的金属内核进行了取样,在这项研究中已成为一种很有前途的替代物。与 CC(碳质或外太阳系)对应物相比,NC 铁明显缺乏 15N。然而,由于缺乏对内核结晶过程中 N 同位素分馏的了解,这种替代方法的实用性受到了限制。我们利用高压高温实验表明,在与内核结晶相关的条件下,固态和液态金属之间的平衡N同位素分馏(Δ15Nsolid-liquid = δ15Nsolid - δ15Nliquid)是有限的(≤1.2 ‰)。这一点,再加上N的亲硒特性以及在核心-幔块分异过程中有限的平衡N同位素分馏,表明铁陨石的δ15N值准确地代表了其母体的N同位素组成。NC铁陨石和CC铁陨石的N同位素比值的变化可归因于母体过程对有机前体的影响,而NC铁陨石相对于CC铁陨石的贫15N性质则不同,它可能为最早的太阳系内行星和外行星的不同N同位素组成提供了最确切的证据。地球原始地幔的 N 同位素组成(δ15N = <-40‰)表明,它保留了早期贫 15N NC 铁陨石母体类星体吸积的记忆。早期吸积的贫15N氮可能储存在深地幔中,或被分离到地核中,或在撞击造成的大气流失过程中流失到太空中。这一特征被随后的CC物质的吸积和混合所覆盖,这反映在地球大气(δ15N = 0)和对流地幔(δ15N = -5‰)相对富含15N的性质上。
Tracing the origin of volatiles on Earth using nitrogen isotope ratios in iron meteorites
Understanding the relationships between the nitrogen (N) isotope ratios of early solar system planetesimals and terrestrial reservoirs is crucial for tracing the origin of volatiles on Earth. The Earth primarily grew from planetesimals and planetary embryos that accreted rapidly (within ∼1–2 Ma after CAIs) in the inner solar system, also known as the non-carbonaceous (NC) reservoir. Magmatic iron meteorites, which sample the metallic cores of the earliest solar system planetesimals, have emerged as a promising proxy in this exercise. NC irons are distinctly 15N-poor compared to their CC (carbonaceous or outer solar system) counterparts. However, the utility of this proxy is limited by the lack of knowledge of N isotope fractionation during core crystallization. Using high pressure-high temperature experiments, we show that equilibrium N isotopic fractionation between solid and liquid metal (Δ15Nsolid–liquid = δ15Nsolid − δ15Nliquid) is limited (≤1.2 ‰) under conditions relevant for core crystallization. This, combined with the siderophile character of N and limited equilibrium N isotope fractionation during core-mantle differentiation, suggests that the δ15N values of iron meteorites accurately represent the N isotopic composition of their parent bodies. Unlike the variation in the N isotope ratios of NC and CC chondrites, which can be attributed to the effects of parent-body processes acting on organic precursors, the 15N-poor nature of NC irons relative to CC irons likely offers the most definitive evidence for the distinct N isotopic compositions of the earliest inner and outer solar system planetesimals. The N isotopic composition of Earth’s primordial mantle (δ15N = <−40 ‰) suggests that it retains the memory of the early accretion of 15N-poor NC iron meteorite parent body-like planetesimals. The early accreted 15N-poor nitrogen may be stored in the deep mantle, segregated into the core, or lost to space during atmospheric loss caused by impacts. This signature was overprinted by the subsequent accretion and admixing of CC materials, which is reflected in the relatively 15N-rich nature of Earth’s atmosphere (δ15N = 0) and convecting mantle (δ15N = −5 ‰).
期刊介绍:
Geochimica et Cosmochimica Acta publishes research papers in a wide range of subjects in terrestrial geochemistry, meteoritics, and planetary geochemistry. The scope of the journal includes:
1). Physical chemistry of gases, aqueous solutions, glasses, and crystalline solids
2). Igneous and metamorphic petrology
3). Chemical processes in the atmosphere, hydrosphere, biosphere, and lithosphere of the Earth
4). Organic geochemistry
5). Isotope geochemistry
6). Meteoritics and meteorite impacts
7). Lunar science; and
8). Planetary geochemistry.