Mars exploration is focused on seeking evidence of habitable environments and microbial life. Terrestrial glassy basalts may be the closest Mars‐surface weathering analog and observations increasingly indicate their potential to preserve biogeochemical records. The textures, major and trace element geochemistry, and N concentrations and isotopic compositions of subaerial, subglacial and continental lacustrine hyaloclastites from Antarctica, Iceland, and Oregon, respectively, were studied using micro‐imaging and chemical methods, including gas‐source mass spectrometry. Alteration by meteoric‐sourced waters occurred in circum‐neutral, increasingly alkaline low‐temperature conditions of ∼60°C–100°C (Iceland) and ∼60°C–170°C (Antarctica). Incompatible large ion lithophile element (LILE) enrichments compared to mid‐ocean ridge basalt (MORB) are consistent with more advanced alteration in Antarctic breccias consisting of heulandite‐clinoptilolite, calcite, erionite, quartz, and fluorapophyllite. Granular and tubular alteration textures and radial apatite represent possible microbial traces. Most samples contain more N than fresh MORB or ocean island basalt reflecting enrichment beyond concentrations attributable to igneous processes. Antarctic samples contain 52–1,143 ppm N and have δ15Νairvalues of −20.8‰ to −7.1‰. Iceland‐Oregon basalts contain 1.6–172 ppm N with δ15Ν of −6.7‰ to +7.3‰. Correlations between alteration extents, N concentrations, and concentrations of K2O, other LILEs, and Li and B, reflect the siting of secondary N likely as NH4+replacing K+and potentially as N2in phyllosilicates and zeolites. Although much of the N enrichment and isotope fractionation presented here is not definitively biogenic, given several unknown factors, we suggest that a combination of textures, major and trace element alteration and N and other isotope geochemical compositions could constitute a compelling biosignature in samples from Mars' surface/near‐surface.
The major ion chemistry of the ocean has been assumed to be controlled by river input, hydrothermal circulation at mid-ocean ridges, carbonate production, and low-temperature alteration of seafloor basalt, but marine chemical budgets remain difficult to balance. Here we propose that large-scale groundwater flow and diagenetic reactions in continental shelf sediments have been overlooked as an important contributor to major ion budgets in the ocean. Based on data synthesized from 17 passive margin basins, continental shelves contribute fluid exchanges comparable to hydrothermal circulation at mid-ocean ridges. Chemical exchange is similarly significant, indicating removal of Mg2+from the oceans at rates similar to mid-ocean ridge convection. Continental shelves likely contribute Ca2+and K+to the oceans at rates that, in combination with low-temperature basalt alteration, can close current budget deficits. Flow and reaction in continental shelf sediments should be included in a new generation of studies addressing marine isotope budgets.
more » « less- NSF-PAR ID:
- 10489922
- Publisher / Repository:
- Nature Publishing Group
- Date Published:
- Journal Name:
- Nature Communications
- Volume:
- 15
- Issue:
- 1
- ISSN:
- 2041-1723
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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