Tracing highly siderophile elements through subduction: Insights from high-pressure serpentinites and 'hybrid' rocks from alpine corsica

The highly siderophile elements (HSE) include the economically critical platinum group elements (PGE; Os, Ir, Ru, Rh, Pt, Pd, Au and Re), gold and rhenium. The HSE are redox sensitive in mantle and seafloor environments and have a strong affinity to iron and sulphur, therefore their distribution wit...

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Main Authors: Crossley, R.J., Evans, Katy, Evans, Noreen, Bragagni, A., McDonald, B.J., Reddy, Steven, Speelmanns, I.M.
Format: Journal Article
Language:English
Published: OXFORD UNIV PRESS 2020
Subjects:
Online Access:http://purl.org/au-research/grants/arc/FF12000579
http://hdl.handle.net/20.500.11937/91765
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author Crossley, R.J.
Evans, Katy
Evans, Noreen
Bragagni, A.
McDonald, B.J.
Reddy, Steven
Speelmanns, I.M.
author_facet Crossley, R.J.
Evans, Katy
Evans, Noreen
Bragagni, A.
McDonald, B.J.
Reddy, Steven
Speelmanns, I.M.
author_sort Crossley, R.J.
building Curtin Institutional Repository
collection Online Access
description The highly siderophile elements (HSE) include the economically critical platinum group elements (PGE; Os, Ir, Ru, Rh, Pt, Pd, Au and Re), gold and rhenium. The HSE are redox sensitive in mantle and seafloor environments and have a strong affinity to iron and sulphur, therefore their distribution within the subducted mantle lithosphere record changes to oxidation state and sulphidation. The mobility of the HSE during subduction has important implications for Re-Os isotopic signatures in the mantle, and the formation of Cu-Au arc-related ore deposits. In this study, subducted rock samples from Alpine Corsica are used to track the HSE in serpentinites and hybrid ultramafic-mafic rocks through the subduction cycle. A comparison of bulk-rock HSE concentrations with those in pre-subduction analogues provides insights into the transfer of the HSE throughout the subduction cycle. Serpentinites subducted to blueschist-eclogite-facies conditions have similar HSE concentrations to primitive upper mantle (PUM) concentrations, therefore it is concluded that the HSE are not mobilized from serpentinites on the scale of the whole-rock or greater. Therefore, as suggested in previous studies, crustal lithologies may be more important contributors of the HSE to the sub-arc mantle, particularly Pt, Pd and Re. In contrast, HSE concentrations in hybrid rocks (talc schist and chlorite schist) deviate from protolith concentrations. Rhenium is higher in the talc schist, and Ir and Ru are lower in the chlorite schist than in the PUM, or possible mafic protoliths. Mineral parageneses place temporal constraints on the growth of hosts to the HSE (sulphides, oxides and metal alloys), and record changes to the activities of oxygen and sulphur (aO2-aS2), and hence redox conditions, from pre-subduction to exhumation. Laser ablation inductively coupled plasma mass spectrometry was used to determine the HSE concentrations in sulphides and oxides, and the detection of small (2-25 mm2) platinum group minerals utilized high-resolution SEM mapping techniques. The prograde and retrograde sulphides have lower HSE concentrations compared with sulphides from pre-subduction settings. Therefore, the redistribution of the HSE on a mineral scale from sulphides to alloys and/or other sulphides has occurred within the serpentinites, which may reflect more reducing conditions during serpentinization or subduction, consistent with the results of thermodynamic modelling. In contrast, the mineral assemblages in the hybrid rocks imply an increase in the extent of sulphidation and oxidation, and higher fluid:rock ratios during exhumation, coincident with Re enrichment in the talc schist, and a decrease in the concentrations of Ir and Ru in the chlorite schist, at length scales greater than those of the rock samples. Therefore, hybridization of lithologies at the slab-mantle interface may enhance the transfer of the HSE to the sub-arc mantle. If Re transfer from the slab to the sub-arc mantle is possible, this questions the robustness of Re-Os isotope signatures as tracers of crustal recycling.
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spelling curtin-20.500.11937-917652023-06-06T03:44:27Z Tracing highly siderophile elements through subduction: Insights from high-pressure serpentinites and 'hybrid' rocks from alpine corsica Crossley, R.J. Evans, Katy Evans, Noreen Bragagni, A. McDonald, B.J. Reddy, Steven Speelmanns, I.M. Science & Technology Physical Sciences Geochemistry & Geophysics highly siderophile elements in situ redox subduction mantle PLATINUM-GROUP ELEMENTS MANTLE-CRUST FRACTIONATION RE-OS FRACTIONATION SILICATE MELT OSMIUM ISOTOPE SULFIDE LIQUID OCEANIC-CRUST PARTITION-COEFFICIENTS CHALCOPHILE ELEMENTS RE/OS FRACTIONATION The highly siderophile elements (HSE) include the economically critical platinum group elements (PGE; Os, Ir, Ru, Rh, Pt, Pd, Au and Re), gold and rhenium. The HSE are redox sensitive in mantle and seafloor environments and have a strong affinity to iron and sulphur, therefore their distribution within the subducted mantle lithosphere record changes to oxidation state and sulphidation. The mobility of the HSE during subduction has important implications for Re-Os isotopic signatures in the mantle, and the formation of Cu-Au arc-related ore deposits. In this study, subducted rock samples from Alpine Corsica are used to track the HSE in serpentinites and hybrid ultramafic-mafic rocks through the subduction cycle. A comparison of bulk-rock HSE concentrations with those in pre-subduction analogues provides insights into the transfer of the HSE throughout the subduction cycle. Serpentinites subducted to blueschist-eclogite-facies conditions have similar HSE concentrations to primitive upper mantle (PUM) concentrations, therefore it is concluded that the HSE are not mobilized from serpentinites on the scale of the whole-rock or greater. Therefore, as suggested in previous studies, crustal lithologies may be more important contributors of the HSE to the sub-arc mantle, particularly Pt, Pd and Re. In contrast, HSE concentrations in hybrid rocks (talc schist and chlorite schist) deviate from protolith concentrations. Rhenium is higher in the talc schist, and Ir and Ru are lower in the chlorite schist than in the PUM, or possible mafic protoliths. Mineral parageneses place temporal constraints on the growth of hosts to the HSE (sulphides, oxides and metal alloys), and record changes to the activities of oxygen and sulphur (aO2-aS2), and hence redox conditions, from pre-subduction to exhumation. Laser ablation inductively coupled plasma mass spectrometry was used to determine the HSE concentrations in sulphides and oxides, and the detection of small (2-25 mm2) platinum group minerals utilized high-resolution SEM mapping techniques. The prograde and retrograde sulphides have lower HSE concentrations compared with sulphides from pre-subduction settings. Therefore, the redistribution of the HSE on a mineral scale from sulphides to alloys and/or other sulphides has occurred within the serpentinites, which may reflect more reducing conditions during serpentinization or subduction, consistent with the results of thermodynamic modelling. In contrast, the mineral assemblages in the hybrid rocks imply an increase in the extent of sulphidation and oxidation, and higher fluid:rock ratios during exhumation, coincident with Re enrichment in the talc schist, and a decrease in the concentrations of Ir and Ru in the chlorite schist, at length scales greater than those of the rock samples. Therefore, hybridization of lithologies at the slab-mantle interface may enhance the transfer of the HSE to the sub-arc mantle. If Re transfer from the slab to the sub-arc mantle is possible, this questions the robustness of Re-Os isotope signatures as tracers of crustal recycling. 2020 Journal Article http://hdl.handle.net/20.500.11937/91765 10.1093/petrology/egaa030 English http://purl.org/au-research/grants/arc/FF12000579 http://purl.org/au-research/grants/arc/CE1101017 http://purl.org/au-research/grants/arc/LE140100150 OXFORD UNIV PRESS fulltext
spellingShingle Science & Technology
Physical Sciences
Geochemistry & Geophysics
highly siderophile elements
in situ
redox
subduction
mantle
PLATINUM-GROUP ELEMENTS
MANTLE-CRUST FRACTIONATION
RE-OS FRACTIONATION
SILICATE MELT
OSMIUM ISOTOPE
SULFIDE LIQUID
OCEANIC-CRUST
PARTITION-COEFFICIENTS
CHALCOPHILE ELEMENTS
RE/OS FRACTIONATION
Crossley, R.J.
Evans, Katy
Evans, Noreen
Bragagni, A.
McDonald, B.J.
Reddy, Steven
Speelmanns, I.M.
Tracing highly siderophile elements through subduction: Insights from high-pressure serpentinites and 'hybrid' rocks from alpine corsica
title Tracing highly siderophile elements through subduction: Insights from high-pressure serpentinites and 'hybrid' rocks from alpine corsica
title_full Tracing highly siderophile elements through subduction: Insights from high-pressure serpentinites and 'hybrid' rocks from alpine corsica
title_fullStr Tracing highly siderophile elements through subduction: Insights from high-pressure serpentinites and 'hybrid' rocks from alpine corsica
title_full_unstemmed Tracing highly siderophile elements through subduction: Insights from high-pressure serpentinites and 'hybrid' rocks from alpine corsica
title_short Tracing highly siderophile elements through subduction: Insights from high-pressure serpentinites and 'hybrid' rocks from alpine corsica
title_sort tracing highly siderophile elements through subduction: insights from high-pressure serpentinites and 'hybrid' rocks from alpine corsica
topic Science & Technology
Physical Sciences
Geochemistry & Geophysics
highly siderophile elements
in situ
redox
subduction
mantle
PLATINUM-GROUP ELEMENTS
MANTLE-CRUST FRACTIONATION
RE-OS FRACTIONATION
SILICATE MELT
OSMIUM ISOTOPE
SULFIDE LIQUID
OCEANIC-CRUST
PARTITION-COEFFICIENTS
CHALCOPHILE ELEMENTS
RE/OS FRACTIONATION
url http://purl.org/au-research/grants/arc/FF12000579
http://purl.org/au-research/grants/arc/FF12000579
http://purl.org/au-research/grants/arc/FF12000579
http://hdl.handle.net/20.500.11937/91765