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Abiotic nitrogen reduction on the early Earth

Author

Listed:
  • Jay A. Brandes

    (Geophysical Laboratory, Carnegie Institution of Washington)

  • Nabil Z. Boctor

    (Geophysical Laboratory, Carnegie Institution of Washington)

  • George D. Cody

    (Geophysical Laboratory, Carnegie Institution of Washington)

  • Benjamin A. Cooper

    (Geophysical Laboratory, Carnegie Institution of Washington)

  • Robert M. Hazen

    (Geophysical Laboratory, Carnegie Institution of Washington)

  • Hatten S. Yoder

    (Geophysical Laboratory, Carnegie Institution of Washington)

Abstract

The production of organic precursors to life depends critically onthe form of the reactants. In particular, an environment dominated by N2 is far less efficient in synthesizing nitrogen-bearing organics than a reducing environment rich in ammonia (refs 1, 2). Relatively reducing lithospheric conditions on the early Earth have been presumed to favour the generation of an ammonia-rich atmosphere, but this hypothesis has not been studied experimentally. Here we demonstrate mineral-catalysed reduction of N2, NO2− and NO3− to ammonia at temperatures between 300 and 800 °C and pressures of 0.1–0.4 GPa — conditions typical of crustal and oceanic hydrothermal systems. We also show that only N2 is stable above 800 °C, thus precluding significant atmospheric ammonia formation during hot accretion. We conclude that mineral-catalysed N2 reduction might have provided a significant source of ammonia to the Hadean ocean. These results also suggest that, whereas nitrogen in the Earth's early atmosphere was present predominantly as N2, exchange with oceanic, hydrothermally derived ammonia could have provided a significant amount of the atmospheric ammonia necessary to resolve the early-faint-Sun paradox3.

Suggested Citation

  • Jay A. Brandes & Nabil Z. Boctor & George D. Cody & Benjamin A. Cooper & Robert M. Hazen & Hatten S. Yoder, 1998. "Abiotic nitrogen reduction on the early Earth," Nature, Nature, vol. 395(6700), pages 365-367, September.
  • Handle: RePEc:nat:nature:v:395:y:1998:i:6700:d:10.1038_26450
    DOI: 10.1038/26450
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