Influence of high marine Ca/SO4 ratio on alteration of submarine basalts at 2.41 Ga documented by triple O and Sr isotopes of epidote

D. O. Zakharov, C. C. Lundstrom, O. Laurent, M. H. Reed, I. N. Bindeman

Research output: Contribution to journalArticlepeer-review

Abstract

Over the course of Earth's history, marine sulfate concentrations have been increasing in response to long-term atmospheric oxygenation. In contrast to modern oceans, where abundant sulfate precipitates in hot oceanic crust as anhydrite, Precambrian oceans contained much less (~0–10 mM) sulfate, so that submarine hydrothermal systems were comparatively poor in anhydrite. As a step towards exploring the role of chemical evolution of seawater solutes, we investigate the reaction between basalt and seawater that took place at the ca. 2.43–2.41 Ga Vetreny Belt (Karelia craton, NW Russia) using fluid inclusion and multi-isotope measurements complemented by reactive transport and static aqueous-mineral equilibrium calculations. Using fluid inclusion measurements by LA-ICP-MS, we constrain the Sr concentration in the least modified seawater-derived fluids and address the effect of phase separation. Then, we complement the previous δ18O – Δ′17O datasets with new 87Sr/86Sr measurements performed on 2.41 Ga epidote from the Vetreny Belt, and recent (0–6 Ma) oceanic epidote from Reykjanes, Iceland and the drilling site 504B in the eastern Pacific Ocean. The 2.41 Ga epidote with 87Sr/86Srinitial of 0.7029–0.7042 and Δ′17O of –0.06 to 0.00‰ is best explained by a relatively high fraction (~90%) of marine Sr that was delivered from contemporaneous seawater with 87Sr/86Sr ≈ 0.7045, and without significant removal by early anhydrite. Using Monte-Carlo simulation of a dual-porosity model, we constrain the range of possible exchange trajectories based on the variability of physical parameters (porosity, fluid flow velocity, fracture spacing, recrystallization rates). Further, we use a series of static equilibrium seawater-basalt reaction calculations with emphasis on the possible range of marine Ca/SO4 values at 2.41 Ga. Our calculations demonstrate that co-existing quartz and epidote in absence of feldspars represent equilibrium with less-evolved hydrothermal fluids. Consequently, equilibrium assemblage of quartz and epidote provide an insightful archive for marine Sr. Based on our modeling and assumptions about marine 87Sr/86Sr and Sr/Ca ratios, the 2.41 Ga epidotes document a seawater-basalt reaction where the initial fluid contained between 30 and 40 mM of Ca and 0–10 mM SO4, representing a high marine input and the possible effect of phase separation. Based on our data, we suggest that high Ca/SO4 ratio of seawater (≫1) and low concentration of anhydrite in submarine systems of the contemporaneous oceans promote a higher fraction of seawater Sr to be permanently stored in silicates of altered oceanic crust. In contrast, modern altered oceanic crust is depleted in radiogenic Sr due to partitioning into anhydrite, which partly returns into the ocean upon cooling.

Original languageEnglish (US)
Article number106164
JournalPrecambrian Research
Volume358
DOIs
StatePublished - Jun 15 2021

Keywords

  • Altered oceanic crust
  • Epidote
  • Marine sulfate
  • Mineral-aqueous equilibrium modeling
  • Triple oxygen isotopes

ASJC Scopus subject areas

  • Geology
  • Geochemistry and Petrology

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