Ge/Si and Ge Isotope Fractionation During Glacial and Non-glacial Weathering: Field and Experimental Data From West Greenland

Glacial environments offer the opportunity to study the incipient stages of chemical weathering due to the high availability of finely ground sediments, low water temperatures, and typically short rock-water interaction times. In this study we focused on the geochemical behavior of germanium (Ge) in...

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Main Authors: J. Jotautas Baronas, Douglas E. Hammond, Mia M. Bennett, Olivier Rouxel, Lincoln H. Pitcher, Laurence C. Smith
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-03-01
Series:Frontiers in Earth Science
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/feart.2021.551900/full
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author J. Jotautas Baronas
J. Jotautas Baronas
Douglas E. Hammond
Mia M. Bennett
Mia M. Bennett
Olivier Rouxel
Lincoln H. Pitcher
Laurence C. Smith
author_facet J. Jotautas Baronas
J. Jotautas Baronas
Douglas E. Hammond
Mia M. Bennett
Mia M. Bennett
Olivier Rouxel
Lincoln H. Pitcher
Laurence C. Smith
author_sort J. Jotautas Baronas
collection DOAJ
description Glacial environments offer the opportunity to study the incipient stages of chemical weathering due to the high availability of finely ground sediments, low water temperatures, and typically short rock-water interaction times. In this study we focused on the geochemical behavior of germanium (Ge) in west Greenland, both during subglacial weathering by investigating glacier-fed streams, as well as during a batch reactor experiment by allowing water-sediment interaction for up to 2 years in the laboratory. Sampled in late August 2014, glacial stream Ge and Si concentrations were low, ranging between 12–55 pmol/L and 7–33 µmol/L, respectively (Ge/Si = 0.9–2.2 µmol/mol, similar to parent rock). As reported previously, the dissolved stable Ge isotope ratio (δ74Ge) of the Watson River was 0.86 ± 0.24‰, the lowest among global rivers and streams measured to date. This value was only slightly heavier than the suspended load (0.48 ± 0.23‰), which is likely representative of the bulk parent rock composition. Despite limited Ge/Si and δ74GeGe fractionation, both Ge and Si appear depleted relative to Na during subglacial weathering, which we interpret as the relatively congruent uptake of both phases by amorphous silica (aSi). Continued sediment-water interaction over 470–785 days in the lab produced a large increase in dissolved Si concentrations (up to 130–230 µmol/L), a much smaller increase in dissolved Ge (up to ∼70 pmol/L), resulting in a Ge/Si decrease (to 0.4–0.5 µmol/mol) and a significant increase in δ74Ge (to 1.9–2.2‰). We argue that during the experiment, both Si and Ge are released by the dissolution of previously subglacially formed aSi, and Ge is then incorporated into secondary phases (likely adsorbed to Fe oxyhydroxides), with an associated Δ74Gesecondary−dissolved fractionation factor of −2.15 ± 0.46‰. In summary, we directly demonstrate Ge isotope fractionation during the dissolution-precipitation weathering reactions of natural sediments in the absence of biological Ge and Si uptake, and highlight the significant differences in Ge behavior during subglacial and non-glacial weathering.
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spelling doaj.art-54998dff9f854b23b718ddd95eb5917a2022-12-21T18:35:45ZengFrontiers Media S.A.Frontiers in Earth Science2296-64632021-03-01910.3389/feart.2021.551900551900Ge/Si and Ge Isotope Fractionation During Glacial and Non-glacial Weathering: Field and Experimental Data From West GreenlandJ. Jotautas Baronas0J. Jotautas Baronas1Douglas E. Hammond2Mia M. Bennett3Mia M. Bennett4Olivier Rouxel5Lincoln H. Pitcher6Laurence C. Smith7Department of Earth Sciences, University of Southern California, Los Angeles, CA, United StatesDepartment of Earth Sciences, University of Cambridge, Cambridge, United KingdomDepartment of Earth Sciences, University of Southern California, Los Angeles, CA, United StatesDepartment of Geography, University of California Los Angeles, Los Angeles, CA, United StatesDepartment of Geography, The University of Hong Kong, Hong Kong, ChinaIFREMER, Centre De Brest, Unité Géosciences Marines, Plouzané, FranceDepartment of Geography, University of California Los Angeles, Los Angeles, CA, United StatesDepartment of Geography, University of California Los Angeles, Los Angeles, CA, United StatesGlacial environments offer the opportunity to study the incipient stages of chemical weathering due to the high availability of finely ground sediments, low water temperatures, and typically short rock-water interaction times. In this study we focused on the geochemical behavior of germanium (Ge) in west Greenland, both during subglacial weathering by investigating glacier-fed streams, as well as during a batch reactor experiment by allowing water-sediment interaction for up to 2 years in the laboratory. Sampled in late August 2014, glacial stream Ge and Si concentrations were low, ranging between 12–55 pmol/L and 7–33 µmol/L, respectively (Ge/Si = 0.9–2.2 µmol/mol, similar to parent rock). As reported previously, the dissolved stable Ge isotope ratio (δ74Ge) of the Watson River was 0.86 ± 0.24‰, the lowest among global rivers and streams measured to date. This value was only slightly heavier than the suspended load (0.48 ± 0.23‰), which is likely representative of the bulk parent rock composition. Despite limited Ge/Si and δ74GeGe fractionation, both Ge and Si appear depleted relative to Na during subglacial weathering, which we interpret as the relatively congruent uptake of both phases by amorphous silica (aSi). Continued sediment-water interaction over 470–785 days in the lab produced a large increase in dissolved Si concentrations (up to 130–230 µmol/L), a much smaller increase in dissolved Ge (up to ∼70 pmol/L), resulting in a Ge/Si decrease (to 0.4–0.5 µmol/mol) and a significant increase in δ74Ge (to 1.9–2.2‰). We argue that during the experiment, both Si and Ge are released by the dissolution of previously subglacially formed aSi, and Ge is then incorporated into secondary phases (likely adsorbed to Fe oxyhydroxides), with an associated Δ74Gesecondary−dissolved fractionation factor of −2.15 ± 0.46‰. In summary, we directly demonstrate Ge isotope fractionation during the dissolution-precipitation weathering reactions of natural sediments in the absence of biological Ge and Si uptake, and highlight the significant differences in Ge behavior during subglacial and non-glacial weathering.https://www.frontiersin.org/articles/10.3389/feart.2021.551900/fullglacial weatheringgermaniumisotope fractionationAmorphous silicaexperimental dissolution
spellingShingle J. Jotautas Baronas
J. Jotautas Baronas
Douglas E. Hammond
Mia M. Bennett
Mia M. Bennett
Olivier Rouxel
Lincoln H. Pitcher
Laurence C. Smith
Ge/Si and Ge Isotope Fractionation During Glacial and Non-glacial Weathering: Field and Experimental Data From West Greenland
Frontiers in Earth Science
glacial weathering
germanium
isotope fractionation
Amorphous silica
experimental dissolution
title Ge/Si and Ge Isotope Fractionation During Glacial and Non-glacial Weathering: Field and Experimental Data From West Greenland
title_full Ge/Si and Ge Isotope Fractionation During Glacial and Non-glacial Weathering: Field and Experimental Data From West Greenland
title_fullStr Ge/Si and Ge Isotope Fractionation During Glacial and Non-glacial Weathering: Field and Experimental Data From West Greenland
title_full_unstemmed Ge/Si and Ge Isotope Fractionation During Glacial and Non-glacial Weathering: Field and Experimental Data From West Greenland
title_short Ge/Si and Ge Isotope Fractionation During Glacial and Non-glacial Weathering: Field and Experimental Data From West Greenland
title_sort ge si and ge isotope fractionation during glacial and non glacial weathering field and experimental data from west greenland
topic glacial weathering
germanium
isotope fractionation
Amorphous silica
experimental dissolution
url https://www.frontiersin.org/articles/10.3389/feart.2021.551900/full
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