Abstract

Hydrogen (H2) and oxidants (O2 and H2O2) are naturally produced by radiolysis of water in any environment where water is bombarded by α, β, and γ radiation generated during radioactive decay. The production of radiolytic H2 in aqueous solutions and in some monomineral-water mixtures has been extensively studied. However, yields of radiolytic products in natural materials remain largely unexplored. Quantification of radiolytic production in common geological materials is critical to assess the importance of water radiolysis as source of microbial reductants and oxidants in water-containing subsurface environments. Knowledge of radiolytic production is also fundamental for the nuclear industry, as maintenance and development of nuclear reactors, long-term disposal of radioactive waste and management of mixed-waste storage tanks are intricately associated with radiolysis products. We experimentally quantified H2 yields for α- and γ-irradiation of pure water, seawater, and slurries of marine sediment, montmorillonite, and two natural zeolites (mordenite and clinoptilolite) widely used in the nuclear industry. The sediment samples include the dominant types found in the global ocean (abyssal clay, nannofossil-bearing clay [marl], clay-bearing diatom ooze, and nannofossil ooze). These experiments demonstrate that all common types of marine sediment and both zeolites catalyze radiolytic H2 production. Hydrogen yields [G(H2)] from water radiolysis differ from one geological material to another. They range between 3.43 and 37.54 molecules H2 100eV-1 for α-particles and and 0.27 and 1.96 molecules H2 100eV-1 for γ-rays. Abyssal clay, earth’s most widespread marine sediment type, exhibits the highest yield amplification when exposed to α-particles with an average factor increase of 18 relative to pure water. Siliceous ooze and abyssal clay exhibit the highest H2 yields when exposed to γ-rays, increasing production by factors of up to 8 and 4, respectively. Calcareous ooze (factor 5 amplification) and lithogeneous sediment (17% amplification) exhibit the smallest yield amplification under α-particle and γ-rays irradiation, respectively. Zeolite mineral slurries increase G(H2) for α- and γ-irradiation by factors of 13 and 4, respectively (similar to abyssal clay). Our results show that substrate chemistry and specific surface area are the main factors that control radiolytic H2 production. The mineral-catalysis of radiolytic H2 production has significant implications for: (i) sustenance of Earth’s subsurface microbial ecosystems (ii) habitability of other planetary bodies, and (iii) nuclear industrial activities. In electron equivalents per unit area, radiolytic H2 production in marine sediment locally produces as much electron donor (food) as photosynthetic carbon fixation in the ocean. Although small relative to global

Highlights

  • H2 and H2O2 are continuously generated in wet sediment and rock from splitting of water [2H2O → H2 + H2O2] by radiation from decay of naturally occurring radionuclides [238U, 235U, 232Th, and 40K] (1, 2, 3)

  • We show that all marine sediment efficiently catalyzes H2 production by water radiolysis, amplifying H2 yields by up to a factor of 27 relative to pure water, depending on sediment composition

  • These radiolytic products constitute a continuous source of energy for microbial ecosystems in subsurface environments (6)

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Summary

Sample selection and experimentally quantified radiolytic H2 yields, G(H2)

Bottom water collected in the Hudson Canyon (water depth, 2136 m) during Endeavor expedition EN534 was used. Salinity of North Atlantic bottom water in the vicinity of the Hudson Canyon (salinity 34.96gms/kg) is very close to that of mean openocean bottom water (salinity 34.70 gms/kg) [4,5]. Energy normalized radiolytic H2 yields are commonly expressed as G(H2)-values (molecules H2 per 100eV absorbed) for a given radiation type (9). We calculated G(H2)-values for each sample and radiation type (α or γ) as the slope of the least-square regression line of total adsorbed dose versus radiolytic H2 concentration G(H2)-values for each sample and radiation type (α or γ) are reported in Supp.

Subseafloor radiolytic H2 production rate
Global budget of radiolytic H2 production in marine sediment
Comparison of photosynthetic organic carbon production relative to radiolytic H2 production
Dissolved H2 concentrations Dissolved H2 concentrations for South
Sediment age determination
Findings
Subseafloor radiolytic oxidants production rates and comparison with net DIC production rate at anoxic sites
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