加拿大东北部 Saglek-Hebron 复合地层岩石中的三重氧和氢同位素对海水与大洋地壳相互作用的制约:中度低δ18O 始新世海洋的含义

IF 3.6 2区 地球科学 Q1 GEOCHEMISTRY & GEOPHYSICS Chemical Geology Pub Date : 2024-09-01 DOI:10.1016/j.chemgeo.2024.122378
A. Kutyrev , I.N. Bindeman , J. O'Neil , H. Rizo
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引用次数: 0

摘要

对地球最早地表条件的估算假定,海洋的温度和氧同位素组成之间存在密切联系,地表风化和海底热液蚀变起平衡作用。保存下来的最古老的超坚硬岩石为研究和制约地球最早的地表条件提供了难得的机会。在此,我们介绍了对加拿大拉布拉多北部萨格瑞克-赫布伦复合体中经热液蚀变的新元古代变质玄武岩、超基性岩以及碎屑沉积物和化学沉积物的三重氧和氢同位素的研究。在变质火山岩中,δ'O值从4.83‰到8.56‰不等,而δ'O值则从-0.076‰到-0.023‰不等,既高于地幔,也低于地幔。考虑到变质作用对氧和氢同位素组成的影响,我们证明三重氧同位素值是从热液亚洋阶段保留下来的,而氢同位素组成(δD从-77.9‰到-10.7‰)都不能解释为原生的。来自 Saglek-Hebron 复合体的几个变质岩样本的 Δ'Ο 值低于现代地幔值,这不能用与现代海水的直接相互作用来解释,而表明上游存在复杂的相互作用。我们的数值模型和蒙特卡洛模拟考虑了水-岩石相互作用的一阶段和两阶段机制,包括玄武岩与化学沉积物衍生流体相互作用引起的δ'Ο和δ'Ο同位素偏移效应。建模结果表明,新元古代海水的特点是δ'Ο < -8 ‰,而δ'Ο最高为 0.01 ‰。这个模型也适用于较低 δ'Ο 时的较高Δ'Ο。我们的研究结果还表明,如果不对多阶段的水岩相互作用(包括同位素偏移和沉积物衍生流体的输入)进行适当建模,变化的大洋地壳裸露部分只能呈现原始海水的遥远证据。由于模拟的同位素偏移和流体混合,我们倾向于在全球范围内实现海水与大洋地壳相互作用的 "弱 "耦合。这可能会降低海底热液蚀变在解释整个地质历史中海底玄武岩氧同位素记录方面的相对重要性。
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Seawater-oceanic crust interaction constrained by triple oxygen and hydrogen isotopes in rocks from the Saglek-Hebron complex, NE Canada: Implications for moderately low-δ18O Eoarchean Ocean

Estimations of Earth's earliest surface conditions assume a strong connection between the temperature and oxygen isotopic composition of oceans, balanced by surface weathering and submarine hydrothermal alteration. The oldest preserved supracrustal rocks provide rare opportunities to study and constrain the earliest surface conditions prevailing on the Earth. Here, we present a study of triple oxygen and hydrogen isotopes of hydrothermally altered Eoarchean metamorphosed basalts, ultramafic rocks, and detrital and chemical sediments, from the Saglek-Hebron Complex in northern Labrador, Canada. For the metavolcanic rocks, δ’18O values range from 4.83 ‰ to 8.56 ‰, while Δ’17O values vary from −0.076 ‰ to −0.023 ‰, both higher and lower than the mantle. Accounting for the effects of metamorphism on oxygen and hydrogen isotopic compositions, we demonstrate that triple oxygen isotopic values are preserved from the hydrothermal suboceanic stage, while none of the hydrogen isotope compositions (δD from −77.9 ‰ to −10.7 ‰) are interpreted as primary. Several metabasalt samples from the Saglek-Hebron Complex yielded Δ’17Ο values lower than modern mantle values, which cannot be explained by direct interaction with modern seawater and indicate complex upstream interactions. Our numerical models and Monte Carlo simulation considers one- and two-stage mechanisms of water-rock interaction, including the δ’18Ο and Δ’17Ο isotopic shift effects due to interaction between basalts and chemical sediment-derived fluids. The modelling favors Eoarchean seawater characterized by low δ’18Ο < −8 ‰ at Δ’17Ο up to 0.01 ‰. This model also works for higher Δ’17Ο at lower δ’18Ο. Our results also suggest that without proper modelling of multi-stage water-rock interaction, involving isotopic shifts and input of sediment-derived fluids, exposed sections of altered oceanic crust present only remote evidence of the original seawater. Due to the modeled isotopic shifts and fluid mixing, we favor “weak” coupling of seawater-oceanic crust interaction globally. This potentially reduces the relative importance of submarine hydrothermal alteration in explaining the oxygen isotopic record in submarine basalts across the geologic history.

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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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