Fractionation of rhenium isotopes in the Mackenzie River basin during oxidative weathering

<p>Rhenium (Re) is a trace element whose redox chemistry makes it an ideal candidate to trace a range of geochemical processes. Here, we report the first rhenium isotopic measurements (&delta;<sup>187</sup>Re) from river-borne materials to assess the influence of chemical weath...

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Main Authors: Dellinger, M, Hilton, RG, Nowell, GM
Format: Journal article
Language:English
Published: Elsevier 2021
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author Dellinger, M
Hilton, RG
Nowell, GM
author_facet Dellinger, M
Hilton, RG
Nowell, GM
author_sort Dellinger, M
collection OXFORD
description <p>Rhenium (Re) is a trace element whose redox chemistry makes it an ideal candidate to trace a range of geochemical processes. Here, we report the first rhenium isotopic measurements (&delta;<sup>187</sup>Re) from river-borne materials to assess the influence of chemical weathering on Re isotopes at continental scale. The&nbsp;&delta;<sup>187</sup>Re was measured in water, suspended sediments and bedloads from the Mackenzie River and its main Arctic tributaries in Northwestern Canada. We find that the&nbsp;&delta;<sup>187</sup>Re (relative to NIST SRM 989) of river waters ranges from &minus;0.05&permil; to +0.07&permil;, which is generally higher than the corresponding river sediment (&minus;0.25&permil; to +0.01&permil;). We show that the range of&nbsp;&delta;<sup>187</sup>Re in river sediments (&sim;0.30&permil;) is controlled by a combination of source bedrock isotopic variability (provenance) and modern oxidative weathering processes. After correcting for bedrock variability, the&nbsp;&delta;<sup>187</sup>Re of solids appear to be positively correlated with the amount of Re depletion related to oxidative weathering. This correlation, and the offset in&nbsp;&delta;<sup>187</sup>Re between river water and sediment, can be explained by preferential oxidation of reactive phases with high&nbsp;&delta;<sup>187</sup>Re (i.e. rock organic carbon, sulfide minerals), but could also result from fractionation during oxidation or the influence of secondary weathering processes. Overall, we find that both basin-average bedrock&nbsp;&delta;<sup>187</sup>Re (&sim;&minus;0.05&permil;) and dissolved&nbsp;&delta;<sup>187</sup>Re (&sim;&minus;0.01&permil;) in the Mackenzie River are lower than the&nbsp;&delta;<sup>187</sup>Re of Atlantic seawater (+0.12&permil;). These observations provide impetus for future work to constrain the Re isotope mass balance of seawater, and assess the potential for secular shifts in its&nbsp;&delta;<sup>187</sup>Re values over time, which could provide an additional isotopic proxy to trace current and past redox processes at Earth's Surface.</p>
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spelling oxford-uuid:58addb04-1211-4ca9-9b91-a216c21b40292022-06-22T14:17:37ZFractionation of rhenium isotopes in the Mackenzie River basin during oxidative weatheringJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:58addb04-1211-4ca9-9b91-a216c21b4029EnglishSymplectic ElementsElsevier2021Dellinger, MHilton, RGNowell, GM<p>Rhenium (Re) is a trace element whose redox chemistry makes it an ideal candidate to trace a range of geochemical processes. Here, we report the first rhenium isotopic measurements (&delta;<sup>187</sup>Re) from river-borne materials to assess the influence of chemical weathering on Re isotopes at continental scale. The&nbsp;&delta;<sup>187</sup>Re was measured in water, suspended sediments and bedloads from the Mackenzie River and its main Arctic tributaries in Northwestern Canada. We find that the&nbsp;&delta;<sup>187</sup>Re (relative to NIST SRM 989) of river waters ranges from &minus;0.05&permil; to +0.07&permil;, which is generally higher than the corresponding river sediment (&minus;0.25&permil; to +0.01&permil;). We show that the range of&nbsp;&delta;<sup>187</sup>Re in river sediments (&sim;0.30&permil;) is controlled by a combination of source bedrock isotopic variability (provenance) and modern oxidative weathering processes. After correcting for bedrock variability, the&nbsp;&delta;<sup>187</sup>Re of solids appear to be positively correlated with the amount of Re depletion related to oxidative weathering. This correlation, and the offset in&nbsp;&delta;<sup>187</sup>Re between river water and sediment, can be explained by preferential oxidation of reactive phases with high&nbsp;&delta;<sup>187</sup>Re (i.e. rock organic carbon, sulfide minerals), but could also result from fractionation during oxidation or the influence of secondary weathering processes. Overall, we find that both basin-average bedrock&nbsp;&delta;<sup>187</sup>Re (&sim;&minus;0.05&permil;) and dissolved&nbsp;&delta;<sup>187</sup>Re (&sim;&minus;0.01&permil;) in the Mackenzie River are lower than the&nbsp;&delta;<sup>187</sup>Re of Atlantic seawater (+0.12&permil;). These observations provide impetus for future work to constrain the Re isotope mass balance of seawater, and assess the potential for secular shifts in its&nbsp;&delta;<sup>187</sup>Re values over time, which could provide an additional isotopic proxy to trace current and past redox processes at Earth's Surface.</p>
spellingShingle Dellinger, M
Hilton, RG
Nowell, GM
Fractionation of rhenium isotopes in the Mackenzie River basin during oxidative weathering
title Fractionation of rhenium isotopes in the Mackenzie River basin during oxidative weathering
title_full Fractionation of rhenium isotopes in the Mackenzie River basin during oxidative weathering
title_fullStr Fractionation of rhenium isotopes in the Mackenzie River basin during oxidative weathering
title_full_unstemmed Fractionation of rhenium isotopes in the Mackenzie River basin during oxidative weathering
title_short Fractionation of rhenium isotopes in the Mackenzie River basin during oxidative weathering
title_sort fractionation of rhenium isotopes in the mackenzie river basin during oxidative weathering
work_keys_str_mv AT dellingerm fractionationofrheniumisotopesinthemackenzieriverbasinduringoxidativeweathering
AT hiltonrg fractionationofrheniumisotopesinthemackenzieriverbasinduringoxidativeweathering
AT nowellgm fractionationofrheniumisotopesinthemackenzieriverbasinduringoxidativeweathering