Intra-grain variability of hydrogen and trace elements in rutile

IF 3.6 2区 地球科学 Q1 GEOCHEMISTRY & GEOPHYSICS Chemical Geology Pub Date : 2024-11-05 DOI:10.1016/j.chemgeo.2024.122480
Mona Lueder , Jörg Hermann , Renée Tamblyn , Daniela Rubatto , Pierre Lanari , Thorsten Andreas Markmann
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Abstract

Rutile is a commonly used petrogenetic indicator mineral to determine metamorphic temperatures, ages, host−/source lithologies, geochemical reservoirs, and subduction conditions. However, intra grain variabilities of trace elements in rutile are rarely considered. We performed trace element and hydrogen mapping of rutile to assess zoning and diffusion in natural rutile from various lithologies. Trace element and hydrogen show distinct zoning patterns, with mostly regular zoning in rutile from pegmatites and low-T hydrothermal clefts, and typically irregular zoning in rutile from high-P veins and metamorphic rocks. Whereas no clear patterns of trace element correlations can be identified, hydrogen, tri-, tetra- and pentavalent cations can show the same zoning patterns within single rutile grains, despite different substitution mechanisms. This indicates that hydrogen and trace element incorporation is externally controlled by availability and diffusivity of hydrogen and trace elements within the rock matrix, as well as rutile growth rates. H2O mapping reveals that hydrogen is retained in rutile at temperatures of up to ∼650 °C. Coupled substitution of hydrogen with divalent and trivalent cations requires coupled diffusion processes for charge balance if hydrogen is diffusively re-equilibrated. Slow diffusion rates and thus relatively high temperatures for diffusive closure in rutile lead to retention of primary hydrogen and trace element zoning. At high-T conditions of >650 °C, diffusive re-equilibration of all trace elements can be observed. Complex zoning patterns of Zr in rutile show that Zr incorporation into rutile is not purely temperature dependent. In this study, Zr-undersaturation can lead to inaccurate Zr-in-rutile temperatures of up to ∼35 °C difference from peak formation temperatures within single rutile grains and might be a useful tool to evaluate rutile growth conditions. Niobium and Ta are highly zoned in rutile, leading to extremely variable Nb/Ta ratios within single rutile grains that cannot be reconstructed from single spot analyses. Overall, mapping offers a novel and promising tool to understanding trace element behavior in rutile.
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金红石中氢和微量元素的晶粒内变化
金红石是一种常用的岩石成因指示矿物,用于确定变质温度、年龄、主岩/源岩性、地球化学储层和俯冲条件。然而,人们很少考虑金红石中微量元素的晶粒内变异。我们对金红石进行了微量元素和氢元素绘图,以评估来自不同岩性的天然金红石中的分带和扩散情况。微量元素和氢元素显示出明显的分带模式,伟晶岩和低T热液裂隙中的金红石大多具有规则的分带,而高P矿脉和变质岩中的金红石则具有典型的不规则分带。虽然无法确定微量元素的明确关联模式,但氢、三价、四价和五价阳离子在单个金红石晶粒中可以显示出相同的分带模式,尽管取代机制不同。这表明,氢和微量元素的掺入受岩石基质中氢和微量元素的可用性和扩散性以及金红石生长速度的外部控制。氢氧化物分布图显示,氢在温度高达 ∼650 ℃时仍保留在金红石中。氢与二价和三价阳离子的耦合置换需要耦合扩散过程,如果氢是扩散再平衡的,则需要电荷平衡。金红石中的扩散速率较慢,因此扩散闭合的温度相对较高,这导致了原氢和微量元素分区的保留。在 650 °C 的高温条件下,可以观察到所有微量元素的扩散再平衡。金红石中 Zr 的复杂分带模式表明,金红石中 Zr 的掺入并不完全取决于温度。在这项研究中,Zr过饱和可导致金红石中的Zr温度不准确,与单个金红石晶粒内的峰值形成温度相差高达 ∼ 35 °C,这可能是评估金红石生长条件的有用工具。铌和钽在金红石中高度分区,导致单个金红石晶粒内的铌/钽比率变化极大,无法通过单点分析进行重建。总之,制图为了解金红石中微量元素的行为提供了一种新颖而有前途的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Chemical Geology
Chemical Geology 地学-地球化学与地球物理
CiteScore
7.20
自引率
10.30%
发文量
374
审稿时长
3.6 months
期刊介绍: Chemical Geology is an international journal that publishes original research papers on isotopic and elemental geochemistry, geochronology and cosmochemistry. The Journal focuses on chemical processes in igneous, metamorphic, and sedimentary petrology, low- and high-temperature aqueous solutions, biogeochemistry, the environment and cosmochemistry. Papers that are field, experimentally, or computationally based are appropriate if they are of broad international interest. The Journal generally does not publish papers that are primarily of regional or local interest, or which are primarily focused on remediation and applied geochemistry. The Journal also welcomes innovative papers dealing with significant analytical advances that are of wide interest in the community and extend significantly beyond the scope of what would be included in the methods section of a standard research paper.
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