Fe(II) stability in coastal seawater during experiments in Patagonia, Svalbard, and Gran Canaria
<p>The speciation of dissolved iron (DFe) in the ocean is widely assumed to consist almost exclusively of Fe(III)-ligand complexes. Yet in most aqueous environments a poorly defined fraction of DFe also exists as Fe(II), the speciation of which is uncertain. Here we deploy flow injection analy...
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2020-03-01
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doaj-6a42d39fde6f4c12a9060a0df8d8f0af2020-11-25T03:11:54ZengCopernicus PublicationsBiogeosciences1726-41701726-41892020-03-01171327134210.5194/bg-17-1327-2020Fe(II) stability in coastal seawater during experiments in Patagonia, Svalbard, and Gran CanariaM. J. Hopwood0C. Santana-González1J. Gallego-Urrea2N. Sanchez3E. P. Achterberg4M. V. Ardelan5M. Gledhill6M. González-Dávila7L. Hoffmann8Ø. Leiknes9J. M. Santana-Casiano10T. M. Tsagaraki11D. Turner12GEOMAR Helmholtz Centre for Ocean Research Kiel, Kiel, GermanyInstituto de Oceanografía y Cambio Global, IOCAG, Universidad de Las Palmas de Gran Canaria, ULPGC, Las Palmas, SpainDepartment of Marine Sciences, Kristineberg Marine Research Station, University of Gothenburg, Gothenburg, SwedenNorwegian University of Science and Technology, Trondheim, Trondheim, NorwayGEOMAR Helmholtz Centre for Ocean Research Kiel, Kiel, GermanyNorwegian University of Science and Technology, Trondheim, Trondheim, NorwayGEOMAR Helmholtz Centre for Ocean Research Kiel, Kiel, GermanyInstituto de Oceanografía y Cambio Global, IOCAG, Universidad de Las Palmas de Gran Canaria, ULPGC, Las Palmas, SpainDepartment of Chemistry, University of Otago, Dunedin, New ZealandNorwegian University of Science and Technology, Trondheim, Trondheim, NorwayInstituto de Oceanografía y Cambio Global, IOCAG, Universidad de Las Palmas de Gran Canaria, ULPGC, Las Palmas, SpainDepartment of Biological Sciences, University of Bergen, Bergen, NorwayDepartment of Marine Sciences, University of Gothenburg, Gothenburg, Sweden<p>The speciation of dissolved iron (DFe) in the ocean is widely assumed to consist almost exclusively of Fe(III)-ligand complexes. Yet in most aqueous environments a poorly defined fraction of DFe also exists as Fe(II), the speciation of which is uncertain. Here we deploy flow injection analysis to measure in situ Fe(II) concentrations during a series of mesocosm/microcosm/multistressor experiments in coastal environments in addition to the decay rate of this Fe(II) when moved into the dark. During five mesocosm/microcosm/multistressor experiments in Svalbard and Patagonia, where dissolved (0.2 <span class="inline-formula">µ</span>m) Fe and Fe(II) were quantified simultaneously, Fe(II) constituted 24 %–65 % of DFe, suggesting that Fe(II) was a large fraction of the DFe pool. When this Fe(II) was allowed to decay in the dark, the vast majority of measured oxidation rate constants were less than calculated constants derived from ambient temperature, salinity, pH, and dissolved <span class="inline-formula">O<sub>2</sub></span>. The oxidation rates of Fe(II) spikes added to Atlantic seawater more closely matched calculated rate constants. The difference between observed and theoretical decay rates in Svalbard and Patagonia was most pronounced at Fe(II) concentrations <span class="inline-formula"><2</span> nM, suggesting that the effect may have arisen from organic Fe(II) ligands. This apparent enhancement of Fe(II) stability under post-bloom conditions and the existence of such a high fraction of DFe as Fe(II) challenge the assumption that DFe speciation in coastal seawater is dominated by ligand bound-Fe(III) species.</p>https://www.biogeosciences.net/17/1327/2020/bg-17-1327-2020.pdf |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
M. J. Hopwood C. Santana-González J. Gallego-Urrea N. Sanchez E. P. Achterberg M. V. Ardelan M. Gledhill M. González-Dávila L. Hoffmann Ø. Leiknes J. M. Santana-Casiano T. M. Tsagaraki D. Turner |
spellingShingle |
M. J. Hopwood C. Santana-González J. Gallego-Urrea N. Sanchez E. P. Achterberg M. V. Ardelan M. Gledhill M. González-Dávila L. Hoffmann Ø. Leiknes J. M. Santana-Casiano T. M. Tsagaraki D. Turner Fe(II) stability in coastal seawater during experiments in Patagonia, Svalbard, and Gran Canaria Biogeosciences |
author_facet |
M. J. Hopwood C. Santana-González J. Gallego-Urrea N. Sanchez E. P. Achterberg M. V. Ardelan M. Gledhill M. González-Dávila L. Hoffmann Ø. Leiknes J. M. Santana-Casiano T. M. Tsagaraki D. Turner |
author_sort |
M. J. Hopwood |
title |
Fe(II) stability in coastal seawater during experiments in Patagonia, Svalbard, and Gran Canaria |
title_short |
Fe(II) stability in coastal seawater during experiments in Patagonia, Svalbard, and Gran Canaria |
title_full |
Fe(II) stability in coastal seawater during experiments in Patagonia, Svalbard, and Gran Canaria |
title_fullStr |
Fe(II) stability in coastal seawater during experiments in Patagonia, Svalbard, and Gran Canaria |
title_full_unstemmed |
Fe(II) stability in coastal seawater during experiments in Patagonia, Svalbard, and Gran Canaria |
title_sort |
fe(ii) stability in coastal seawater during experiments in patagonia, svalbard, and gran canaria |
publisher |
Copernicus Publications |
series |
Biogeosciences |
issn |
1726-4170 1726-4189 |
publishDate |
2020-03-01 |
description |
<p>The speciation of dissolved iron (DFe) in the ocean is widely
assumed to consist almost exclusively of Fe(III)-ligand complexes. Yet in
most aqueous environments a poorly defined fraction of DFe also exists as
Fe(II), the speciation of which is uncertain. Here we deploy flow injection
analysis to measure in situ Fe(II) concentrations during a series
of mesocosm/microcosm/multistressor experiments in coastal environments in
addition to the decay rate of this Fe(II) when moved into the dark. During
five mesocosm/microcosm/multistressor experiments in Svalbard and Patagonia,
where dissolved (0.2 <span class="inline-formula">µ</span>m) Fe and Fe(II) were quantified
simultaneously, Fe(II) constituted 24 %–65 % of DFe, suggesting that
Fe(II) was a large fraction of the DFe pool. When this Fe(II) was allowed to
decay in the dark, the vast majority of measured oxidation rate constants
were less than calculated constants derived from ambient temperature,
salinity, pH, and dissolved
<span class="inline-formula">O<sub>2</sub></span>. The oxidation rates of Fe(II) spikes added to Atlantic seawater
more closely matched calculated rate constants. The difference between
observed and theoretical decay rates in Svalbard and Patagonia was most
pronounced at Fe(II) concentrations <span class="inline-formula"><2</span> nM, suggesting that the effect may
have arisen from organic Fe(II) ligands. This apparent enhancement of Fe(II)
stability under post-bloom conditions and the existence of such a high
fraction of DFe as Fe(II) challenge the assumption that DFe speciation in
coastal seawater is dominated by ligand bound-Fe(III) species.</p> |
url |
https://www.biogeosciences.net/17/1327/2020/bg-17-1327-2020.pdf |
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