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Partitioning of Fe2O3 in peridotite partial melting experiments over a range of oxygen fugacities elucidates ferric iron systematics in mid-ocean ridge basalts and ferric iron content of the upper mantle

Fred A. Davis, Elizabeth Cottrell

2021Contributions to Mineralogy and Petrology37 citationsDOIOpen Access PDF

Abstract

Abstract Basalts and peridotites from mid-ocean ridges record f O2 near the quartz-fayalite-magnetite buffer (QFM), but peridotite partial melting experiments have mostly been performed in graphite capsules (~ QFM-3), precluding evaluation of ferric iron’s behavior during basalt generation. We performed experiments at 1.5 GPa, 1350–1400 °C, and f O2 from about QFM-3 to QFM+3 to investigate the anhydrous partitioning behavior of Fe 2 O 3 between silicate melts and coexisting peridotite mineral phases. We find spinel/melt partitioning of Fe 2 O 3 ( $${D}_{\mathrm{Fe}2\mathrm{O}3}^{\mathrm{spl}/\mathrm{melt}}$$ <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"> <mml:msubsup> <mml:mi>D</mml:mi> <mml:mrow> <mml:mi>Fe</mml:mi> <mml:mn>2</mml:mn> <mml:mi>O</mml:mi> <mml:mn>3</mml:mn> </mml:mrow> <mml:mrow> <mml:mi>spl</mml:mi> <mml:mo>/</mml:mo> <mml:mi>melt</mml:mi> </mml:mrow> </mml:msubsup> </mml:math> ) increases as spinel Fe 2 O 3 concentrations increase, independent of increases in f O2 , and decreases with temperature, which is consistent with new and previous experiments at 0.1 MPa. We find $${D}_{\mathrm{Fe}2\mathrm{O}3}^{\mathrm{opx}/\mathrm{melt}}$$ <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"> <mml:msubsup> <mml:mi>D</mml:mi> <mml:mrow> <mml:mi>Fe</mml:mi> <mml:mn>2</mml:mn> <mml:mi>O</mml:mi> <mml:mn>3</mml:mn> </mml:mrow> <mml:mrow> <mml:mi>opx</mml:mi> <mml:mo>/</mml:mo> <mml:mi>melt</mml:mi> </mml:mrow> </mml:msubsup> </mml:math> = 0.63 ± 0.10 and $${D}_{\mathrm{Fe}2\mathrm{O}3}^{\mathrm{cpx}/\mathrm{melt}}$$ <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"> <mml:msubsup> <mml:mi>D</mml:mi> <mml:mrow> <mml:mi>Fe</mml:mi> <mml:mn>2</mml:mn> <mml:mi>O</mml:mi> <mml:mn>3</mml:mn> </mml:mrow> <mml:mrow> <mml:mi>cpx</mml:mi> <mml:mo>/</mml:mo> <mml:mi>melt</mml:mi> </mml:mrow> </mml:msubsup> </mml:math> = 0.78 ± 0.30. MORB Fe 2 O 3 and Na 2 O concentrations are consistent with a modeled MORB source with Fe 2 O 3 = 0.48 ± 0.03 wt% (Fe 3+ /ΣFe = 0.053 ± 0.003) at potential temperatures ( T P ) from 1320 to 1440 °C. The temperature-dependence of the $${D}_{\mathrm{Fe}2\mathrm{O}3}^{\mathrm{spl}/\mathrm{melt}}$$ <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"> <mml:msubsup> <mml:mi>D</mml:mi> <mml:mrow> <mml:mi>Fe</mml:mi> <mml:mn>2</mml:mn> <mml:mi>O</mml:mi> <mml:mn>3</mml:mn> </mml:mrow> <mml:mrow> <mml:mi>spl</mml:mi> <mml:mo>/</mml:mo> <mml:mi>melt</mml:mi> </mml:mrow> </mml:msubsup> </mml:math> function alone allows ~ 40% of the variation in MORB compositions. If we allow $${D}_{\mathrm{Fe}2\mathrm{O}3}^{\mathrm{opx}/\mathrm{melt}}$$ <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"> <mml:msubsup> <mml:mi>D</mml:mi> <mml:mrow> <mml:mi>Fe</mml:mi> <mml:mn>2</mml:mn> <mml:mi>O</mml:mi> <mml:mn>3</mml:mn> </mml:mrow> <mml:mrow> <mml:mi>opx</mml:mi> <mml:mo>/</mml:mo> <mml:mi>melt</mml:mi> </mml:mrow> </mml:msubsup> </mml:math> and $${D}_{\mathrm{Fe}2\mathrm{O}3}^{\mathrm{opx}/\mathrm{melt}}$$ <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"> <mml:msubsup> <mml:mi>D</mml:mi> <mml:mrow> <mml:mi>Fe</mml:mi> <mml:mn>2</mml:mn> <mml:mi>O</mml:mi> <mml:mn>3</mml:mn> </mml:mrow> <mml:mrow> <mml:mi>opx</mml:mi> <mml:mo>/</mml:mo> <mml:mi>melt</mml:mi> </mml:mrow> </mml:msubsup> </mml:math> to also vary with temperature by tying them to spinel Fe 2 O 3 through intermineral partitioning, then all the MORB data are within error of the model. Our model Fe 2 O 3 concentration for the MORB source would require that the convecting mantle be more oxidized at a given depth than recorded by continental mantle xenoliths. Our result is supported by thermodynamic models of mantle with Fe 3+ /ΣFe = 0.03 that predict f O2 of ~ QFM-1 near the garnet-spinel transition, which is inconsistent with f O2 of MORB. Our results support previous suggestions that redox melting may occur between 200 and 250 km depth.

Topics & Concepts

GeologyPeridotiteMantle (geology)MineralogyMineral redox bufferSpinelAnalytical Chemistry (journal)ChemistryGeochemistryChromatographyPaleontologyGeological and Geochemical AnalysisHigh-pressure geophysics and materialsearthquake and tectonic studies
Partitioning of Fe2O3 in peridotite partial melting experiments over a range of oxygen fugacities elucidates ferric iron systematics in mid-ocean ridge basalts and ferric iron content of the upper mantle | Litcius