Polybaric fractional crystallisation of arc magmas: an experimental study simulating trans-crustal magmatic systems

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  • ETH Zürich
  • Université de Lausanne (UNIL)
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OriginalspracheEnglisch
Aufsatznummer3
FachzeitschriftContributions to Mineralogy and Petrology
Jahrgang177
Ausgabenummer1
Frühes Online-Datum7 Dez. 2021
PublikationsstatusVeröffentlicht - Jan. 2022

Abstract

Crystallisation-driven differentiation is one fundamental mechanism proposed to control the compositional evolution of magmas. In this experimental study, we simulated polybaric fractional crystallisation of mantle-derived arc magmas. Various pressure–temperature trajectories were explored to cover a range of potential magma ascent paths and to investigate the role of decompression on phase equilibria and liquid lines of descent (LLD). Fractional crystallisation was approached in a step-wise manner by repetitively synthesising new starting materials chemically corresponding to liquids formed in previous runs. Experiments were performed at temperatures ranging from 1140 to 870 °C with 30 °C steps, and pressure was varied between 0.8 and 0.2 GPa with 0.2 GPa steps. For most fractionation paths, oxygen fugacity (fO 2) was buffered close to the Ni-NiO equilibrium (NNO). An additional fractionation series was conducted at fO 2 corresponding to the Re-ReO 2 buffer (RRO ≈ NNO+2). High-pressure experiments (0.4–0.8 GPa) were run in piston cylinder apparatus while 0.2 GPa runs were conducted in externally heated pressure vessels. Resulting liquid lines of descent follow calc-alkaline differentiation trends where the onset of pronounced silica enrichment coincides with the saturation of amphibole and/or Fe–Ti–oxide. Both pressure and fO 2 exert crucial control on the stability fields of olivine, pyroxene, amphibole, plagioclase, and Fe–Ti–oxide phases and on the differentiation behaviour of arc magmas. Key observations are a shift of the olivine–clinopyroxene cotectic towards more clinopyroxene-rich liquid composition, an expansion of the plagioclase stability field and a decrease of amphibole stability with decreasing pressure. Decompression-dominated ascent trajectories result in liquid lines of descent approaching the metaluminous compositional range observed for typical arc volcanic rocks, while differentiation trends obtained for cooling-dominated trajectories evolve to peraluminous compositions, similar to isobaric liquid lines of descent at elevated pressures. Experiments buffered at RRO provide a closer match with natural calc-alkaline differentiation trends compared to fO 2 conditions close to NNO. We conclude that decompression-dominated fractionation at oxidising conditions represents one possible scenario for arc magma differentiation.

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Polybaric fractional crystallisation of arc magmas: an experimental study simulating trans-crustal magmatic systems. / Marxer, Felix; Ulmer, Peter; Müntener, Othmar.
in: Contributions to Mineralogy and Petrology, Jahrgang 177, Nr. 1, 3, 01.2022.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

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abstract = "Crystallisation-driven differentiation is one fundamental mechanism proposed to control the compositional evolution of magmas. In this experimental study, we simulated polybaric fractional crystallisation of mantle-derived arc magmas. Various pressure–temperature trajectories were explored to cover a range of potential magma ascent paths and to investigate the role of decompression on phase equilibria and liquid lines of descent (LLD). Fractional crystallisation was approached in a step-wise manner by repetitively synthesising new starting materials chemically corresponding to liquids formed in previous runs. Experiments were performed at temperatures ranging from 1140 to 870 °C with 30 °C steps, and pressure was varied between 0.8 and 0.2 GPa with 0.2 GPa steps. For most fractionation paths, oxygen fugacity (fO 2) was buffered close to the Ni-NiO equilibrium (NNO). An additional fractionation series was conducted at fO 2 corresponding to the Re-ReO 2 buffer (RRO ≈ NNO+2). High-pressure experiments (0.4–0.8 GPa) were run in piston cylinder apparatus while 0.2 GPa runs were conducted in externally heated pressure vessels. Resulting liquid lines of descent follow calc-alkaline differentiation trends where the onset of pronounced silica enrichment coincides with the saturation of amphibole and/or Fe–Ti–oxide. Both pressure and fO 2 exert crucial control on the stability fields of olivine, pyroxene, amphibole, plagioclase, and Fe–Ti–oxide phases and on the differentiation behaviour of arc magmas. Key observations are a shift of the olivine–clinopyroxene cotectic towards more clinopyroxene-rich liquid composition, an expansion of the plagioclase stability field and a decrease of amphibole stability with decreasing pressure. Decompression-dominated ascent trajectories result in liquid lines of descent approaching the metaluminous compositional range observed for typical arc volcanic rocks, while differentiation trends obtained for cooling-dominated trajectories evolve to peraluminous compositions, similar to isobaric liquid lines of descent at elevated pressures. Experiments buffered at RRO provide a closer match with natural calc-alkaline differentiation trends compared to fO 2 conditions close to NNO. We conclude that decompression-dominated fractionation at oxidising conditions represents one possible scenario for arc magma differentiation.",
keywords = "Arc magmatism, Calc-alkaline rocks, Fractional crystallisation, Liquid line of descent, Magma differentiation, Polybaric differentiation",
author = "Felix Marxer and Peter Ulmer and Othmar M{\"u}ntener",
note = "Funding Information: We would like to thank Lukas Martin, Eric Reusser, and Julien Allaz for assistance during SEM-EDS and EPMA analyses and Andy Huber, Andreas Jallas, and Thomas Good for technical support in the experimental labs. We are grateful to Tom Sisson, Manuel Pimenta Silva, Olivier Bachmann, and Max Schmidt for constructive and enlightening discussions. Thoughtful and constructive reviews from Mike Krawczynski, Andrea Goltz, and an anonymous reviewer as well as the editorial handling by Dante Canil are gratefully acknowledged. This work was supported by the ETH research grant ETH-14 16-1 covering F.M.",
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journal = "Contributions to Mineralogy and Petrology",
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TY - JOUR

T1 - Polybaric fractional crystallisation of arc magmas: an experimental study simulating trans-crustal magmatic systems

AU - Marxer, Felix

AU - Ulmer, Peter

AU - Müntener, Othmar

N1 - Funding Information: We would like to thank Lukas Martin, Eric Reusser, and Julien Allaz for assistance during SEM-EDS and EPMA analyses and Andy Huber, Andreas Jallas, and Thomas Good for technical support in the experimental labs. We are grateful to Tom Sisson, Manuel Pimenta Silva, Olivier Bachmann, and Max Schmidt for constructive and enlightening discussions. Thoughtful and constructive reviews from Mike Krawczynski, Andrea Goltz, and an anonymous reviewer as well as the editorial handling by Dante Canil are gratefully acknowledged. This work was supported by the ETH research grant ETH-14 16-1 covering F.M.

PY - 2022/1

Y1 - 2022/1

N2 - Crystallisation-driven differentiation is one fundamental mechanism proposed to control the compositional evolution of magmas. In this experimental study, we simulated polybaric fractional crystallisation of mantle-derived arc magmas. Various pressure–temperature trajectories were explored to cover a range of potential magma ascent paths and to investigate the role of decompression on phase equilibria and liquid lines of descent (LLD). Fractional crystallisation was approached in a step-wise manner by repetitively synthesising new starting materials chemically corresponding to liquids formed in previous runs. Experiments were performed at temperatures ranging from 1140 to 870 °C with 30 °C steps, and pressure was varied between 0.8 and 0.2 GPa with 0.2 GPa steps. For most fractionation paths, oxygen fugacity (fO 2) was buffered close to the Ni-NiO equilibrium (NNO). An additional fractionation series was conducted at fO 2 corresponding to the Re-ReO 2 buffer (RRO ≈ NNO+2). High-pressure experiments (0.4–0.8 GPa) were run in piston cylinder apparatus while 0.2 GPa runs were conducted in externally heated pressure vessels. Resulting liquid lines of descent follow calc-alkaline differentiation trends where the onset of pronounced silica enrichment coincides with the saturation of amphibole and/or Fe–Ti–oxide. Both pressure and fO 2 exert crucial control on the stability fields of olivine, pyroxene, amphibole, plagioclase, and Fe–Ti–oxide phases and on the differentiation behaviour of arc magmas. Key observations are a shift of the olivine–clinopyroxene cotectic towards more clinopyroxene-rich liquid composition, an expansion of the plagioclase stability field and a decrease of amphibole stability with decreasing pressure. Decompression-dominated ascent trajectories result in liquid lines of descent approaching the metaluminous compositional range observed for typical arc volcanic rocks, while differentiation trends obtained for cooling-dominated trajectories evolve to peraluminous compositions, similar to isobaric liquid lines of descent at elevated pressures. Experiments buffered at RRO provide a closer match with natural calc-alkaline differentiation trends compared to fO 2 conditions close to NNO. We conclude that decompression-dominated fractionation at oxidising conditions represents one possible scenario for arc magma differentiation.

AB - Crystallisation-driven differentiation is one fundamental mechanism proposed to control the compositional evolution of magmas. In this experimental study, we simulated polybaric fractional crystallisation of mantle-derived arc magmas. Various pressure–temperature trajectories were explored to cover a range of potential magma ascent paths and to investigate the role of decompression on phase equilibria and liquid lines of descent (LLD). Fractional crystallisation was approached in a step-wise manner by repetitively synthesising new starting materials chemically corresponding to liquids formed in previous runs. Experiments were performed at temperatures ranging from 1140 to 870 °C with 30 °C steps, and pressure was varied between 0.8 and 0.2 GPa with 0.2 GPa steps. For most fractionation paths, oxygen fugacity (fO 2) was buffered close to the Ni-NiO equilibrium (NNO). An additional fractionation series was conducted at fO 2 corresponding to the Re-ReO 2 buffer (RRO ≈ NNO+2). High-pressure experiments (0.4–0.8 GPa) were run in piston cylinder apparatus while 0.2 GPa runs were conducted in externally heated pressure vessels. Resulting liquid lines of descent follow calc-alkaline differentiation trends where the onset of pronounced silica enrichment coincides with the saturation of amphibole and/or Fe–Ti–oxide. Both pressure and fO 2 exert crucial control on the stability fields of olivine, pyroxene, amphibole, plagioclase, and Fe–Ti–oxide phases and on the differentiation behaviour of arc magmas. Key observations are a shift of the olivine–clinopyroxene cotectic towards more clinopyroxene-rich liquid composition, an expansion of the plagioclase stability field and a decrease of amphibole stability with decreasing pressure. Decompression-dominated ascent trajectories result in liquid lines of descent approaching the metaluminous compositional range observed for typical arc volcanic rocks, while differentiation trends obtained for cooling-dominated trajectories evolve to peraluminous compositions, similar to isobaric liquid lines of descent at elevated pressures. Experiments buffered at RRO provide a closer match with natural calc-alkaline differentiation trends compared to fO 2 conditions close to NNO. We conclude that decompression-dominated fractionation at oxidising conditions represents one possible scenario for arc magma differentiation.

KW - Arc magmatism

KW - Calc-alkaline rocks

KW - Fractional crystallisation

KW - Liquid line of descent

KW - Magma differentiation

KW - Polybaric differentiation

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U2 - 10.1007/s00410-021-01856-8

DO - 10.1007/s00410-021-01856-8

M3 - Article

VL - 177

JO - Contributions to Mineralogy and Petrology

JF - Contributions to Mineralogy and Petrology

SN - 0010-7999

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ER -

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