TY - JOUR
T1 - Glacial influence on the iron and sulfur cycles in Arctic fjord sediments (Svalbard)
AU - Michaud, Alexander B.
AU - Laufer, Katja
AU - Findlay, Alyssa
AU - Pellerin, André
AU - Antler, Gilad
AU - Turchyn, Alexandra V.
AU - Røy, Hans
AU - Wehrmann, Laura M.
AU - Jørgensen, Bo Barker
N1 - Funding Information: This work was supported by the Danish National Research Foundation [DNRF104]; European Research Council [ERC Advanced Grant #294200 to BBJ]; Danish Council for Independent Research [DFF – 7014-00196 to BBJ]; the Israel Science Foundation [2361/19 to GA]; postdoctoral fellowships from the US-National Science Foundation [EAR-PF1625158 to ABM], DFG [DFG 389371177 to KL], and Marie Skłodowska-Curie European Fellowship [SedSulphOx, MSCA 746872 to AF]. We thank the Alfred Wegener Institute-Institute Paul Emile Victor (AWIPEV) station and staff for housing and excellent logistical support; MS Farm captain Stig Henningsen and first mate, Reidar Sørensen; MS Teisten captain Roar Strand. The Polar Geospatial Center and Brad Herried provided geospatial support under NSF OPP awards 1043681 & 1559691. We thank Tomas Cedhagen for identification of benthic fauna. We appreciate the technical assistance of Jeanette Pederson, Karina Bomholt Oest, Simone Bach Pederson at Aarhus University. We thank all the participants of the 2016 Svalbard KOP 56/RiS 10528 expedition for help with sample collection and providing stimulating discussions. The comments and edits from the associate editor and three anonymous reviewers greatly improved this manuscript. Funding Information: This work was supported by the Danish National Research Foundation [DNRF104]; European Research Council [ERC Advanced Grant #294200 to BBJ]; Danish Council for Independent Research [DFF ? 7014-00196 to BBJ]; the Israel Science Foundation [2361/19 to GA]; postdoctoral fellowships from the US-National Science Foundation [EAR-PF1625158 to ABM], DFG [DFG 389371177 to KL], and Marie Sk?odowska-Curie European Fellowship [SedSulphOx, MSCA 746872 to AF]. We thank the Alfred Wegener Institute-Institute Paul Emile Victor (AWIPEV) station and staff for housing and excellent logistical support; MS Farm captain Stig Henningsen and first mate, Reidar S?rensen; MS Teisten captain Roar Strand. The Polar Geospatial Center and Brad Herried provided geospatial support under NSF OPP awards 1043681 & 1559691. We thank Tomas Cedhagen for identification of benthic fauna. We appreciate the technical assistance of Jeanette Pederson, Karina Bomholt Oest, Simone Bach Pederson at Aarhus University. We thank all the participants of the 2016 Svalbard KOP 56/RiS 10528 expedition for help with sample collection and providing stimulating discussions. The comments and edits from the associate editor and three anonymous reviewers greatly improved this manuscript. Publisher Copyright: © 2020 Elsevier Ltd
PY - 2020/7/1
Y1 - 2020/7/1
N2 - Arctic fjord sediments of Svalbard receive terrestrial material from glacial runoff and organic matter from marine primary productivity. Organic carbon mineralization proceeds primarily through sulfate and iron reduction in the fjord sediment. The ongoing retreat of glaciers in the high Arctic is altering the input of glacial material to the fjords, with unknown consequences for the iron and sulfur cycles in the fjord sediments. We measured sulfate reduction rates in sediment cores and analyzed porewater geochemistry, then compared these results to long-term sediment incubations to determine the rates of iron reduction and sulfide oxidation in three glacially influenced fjords on the west coast of Spitsbergen, Svalbard. Despite an abundance of glacially-sourced Fe(III)-oxide minerals, active sulfate reduction took place throughout the sediment. Analyses of the sulfur and oxygen isotopic composition of porewater sulfate and sulfate concentrations suggest that sulfide produced from biological sulfate reduction is reoxidized to sulfate. Long-term sediment incubations indicated sulfide oxidation at all three stations. The rate of sulfide oxidation was controlled by both the rate of sulfate reduction and the quantity and reactivity of Fe(III)-oxides. In our experimental incubations, we detected a decrease in Fe(III) content of the 0.5 M HCl and ascorbate-extractable fractions, but not in the 6 M HCl fraction, indicating that the highly reactive Fe(III) fraction is utilized by microorganisms and serves as the oxidant for sulfide oxidation. Our results show that sulfide oxidation in glacially-influenced fjord sediments is a wide-spread geochemical process. Further warming will drive glacial retreat onto land, where sediment-laden glacial meltwater will be altered during flow through proglacial streams and lakes before entering the marine environment. Fjord sediments will likely become more sulfidic, as glaciers deliver less particulate, highly-reactive metal oxides to the marine environment.
AB - Arctic fjord sediments of Svalbard receive terrestrial material from glacial runoff and organic matter from marine primary productivity. Organic carbon mineralization proceeds primarily through sulfate and iron reduction in the fjord sediment. The ongoing retreat of glaciers in the high Arctic is altering the input of glacial material to the fjords, with unknown consequences for the iron and sulfur cycles in the fjord sediments. We measured sulfate reduction rates in sediment cores and analyzed porewater geochemistry, then compared these results to long-term sediment incubations to determine the rates of iron reduction and sulfide oxidation in three glacially influenced fjords on the west coast of Spitsbergen, Svalbard. Despite an abundance of glacially-sourced Fe(III)-oxide minerals, active sulfate reduction took place throughout the sediment. Analyses of the sulfur and oxygen isotopic composition of porewater sulfate and sulfate concentrations suggest that sulfide produced from biological sulfate reduction is reoxidized to sulfate. Long-term sediment incubations indicated sulfide oxidation at all three stations. The rate of sulfide oxidation was controlled by both the rate of sulfate reduction and the quantity and reactivity of Fe(III)-oxides. In our experimental incubations, we detected a decrease in Fe(III) content of the 0.5 M HCl and ascorbate-extractable fractions, but not in the 6 M HCl fraction, indicating that the highly reactive Fe(III) fraction is utilized by microorganisms and serves as the oxidant for sulfide oxidation. Our results show that sulfide oxidation in glacially-influenced fjord sediments is a wide-spread geochemical process. Further warming will drive glacial retreat onto land, where sediment-laden glacial meltwater will be altered during flow through proglacial streams and lakes before entering the marine environment. Fjord sediments will likely become more sulfidic, as glaciers deliver less particulate, highly-reactive metal oxides to the marine environment.
KW - Arctic
KW - Fjord
KW - Glacier
KW - Iron reactivity
KW - Sulfate reduction
KW - Sulfide oxidation
KW - Svalbard
UR - http://www.scopus.com/inward/record.url?scp=85078849197&partnerID=8YFLogxK
U2 - https://doi.org/10.1016/j.gca.2019.12.033
DO - https://doi.org/10.1016/j.gca.2019.12.033
M3 - Article
SN - 0016-7037
VL - 280
SP - 423
EP - 440
JO - Geochimica et Cosmochimica Acta
JF - Geochimica et Cosmochimica Acta
ER -