The fate of nitrogen during core-mantle separation on Earth. (15th April 2019)

• Record Type: Journal Article
• Authors: Grewal, Damanveer S.; Dasgupta, Rajdeep; Holmes, Alexandra K.; Costin, Gelu; Li, Yuan; Tsuno, Kyusei
• Is Part Of: Geochimica et cosmochimica acta. Volume 251(2019)
• Page Start: 87
• Page End: 115
• Publication Date: 2019-04-15
• Subjects: Nitrogen -- Early Earth differentiation -- Core formation -- Magma Ocean -- Planet formation -- Atmospheric loss; Geochemistry -- Periodicals; Meteorites -- Periodicals; Géochimie -- Périodiques; Météorites -- Périodiques; Geochemie; Astrochemie; Electronic journals; 551.905
• DOI: 10.1016/j.gca.2019.02.009
• Languages: English
• ISSNs: 0016-7037

Abstract

Abstract: Nitrogen, the most dominant constituent of Earth's atmosphere, is critical for the habitability and existence of life on our planet. However, its distribution between Earth's major reservoirs, which must be largely influenced by the accretion and differentiation processes during its formative years, is poorly known. Sequestration into the metallic core, along with volatility related loss pre- and post-accretion, could be a critical process that can explain the depletion of nitrogen in the Bulk Silicate Earth (BSE) relative to the primitive chondrites. However, the relative effect of different thermodynamic parameters on the alloy-silicate partitioning behavior of nitrogen is not well understood. Here we present equilibrium partitioning data of N between alloy and silicate melt ( D N alloy/silicate ) from 67 new high pressure ( P = 1–6 GPa)-temperature ( T = 1500–2200 °C) experiments under graphite saturated conditions at a wide range of oxygen fugacity (log f O2 ∼ ΔIW −4.2 to −0.8), mafic to ultramafic silicate melt compositions (NBO/T = 0.4 to 2.2), and varying chemical composition of the alloy melts (S and Si contents of 0–32.1 wt.% and 0–3.1 wt.%, respectively). Under relatively oxidizing conditions (∼ΔIW −2.2 to −0.8) nitrogen acts as a siderophile element ( D N alloy/silicate between 1.1 and 52), where D N alloy/silicate decreases with decrease in f O2 and increase in T, and increases with increase in P and NBO/T. Under these conditions D N alloy/silicate remains largely unaffected between S-free conditions and up to ∼17 wt.% S content in the alloy melt, and then drops off at >∼20 wt.% S content in the alloy melt. Under increasingly reduced conditions (<∼ΔIW −2.2), N becomes increasingly lithophile ( D N alloy/silicate between 0.003 and 0.5) with D N alloy/silicate decreasing with decrease in f O2 and increase in T . At these conditions, f O2 along with Si content of the alloy under the most reduced conditions (<∼ΔIW –3.0), is the controlling parameter with T playing a secondary role, while, P, NBO/T, and S content of the alloy have minimal effects. A multiple linear least-squares regression parametrization for D N alloy/silicate based on the results of this study and previous studies suggests, in agreement with the experimental data, that f O2 (represented by Si content of the alloy melt and FeO content of the silicate melt), followed by T, has the strongest control on D N alloy/silicate . Based on our modeling, to match the present-day BSE N content, impactors that brought N must have been moderately to highly oxidized. If N bearing impactors were reduced, and/or there was significant disequilibrium core formation, then the BSE would be too N-rich and another mechanism for N loss, such as atmospheric loss, would be required.