Articles | Volume 21, issue 14
https://doi.org/10.5194/bg-21-3425-2024
© Author(s) 2024. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/bg-21-3425-2024
© Author(s) 2024. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Dissolved nitric oxide in the lower Elbe Estuary and the Port of Hamburg area
Riel Carlo O. Ingeniero
CORRESPONDING AUTHOR
Marine Biogeochemistry Research Division, GEOMAR Helmholtz Centre for Ocean Research Kiel, 24148 Kiel, Germany
Gesa Schulz
Institute of Geology, Universität Hamburg, 20146 Hamburg, Germany
Institute of Carbon Cycles, Helmholtz-Zentrum Hereon, 21502 Geesthacht, Germany
Hermann W. Bange
Marine Biogeochemistry Research Division, GEOMAR Helmholtz Centre for Ocean Research Kiel, 24148 Kiel, Germany
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Atmospheric concentrations of nitrous oxide (N2O), a greenhouse gas 273 times more potent than carbon dioxide, have increased by 25 % since the preindustrial period, with the highest observed growth rate in 2020 and 2021. This rapid growth rate has primarily been due to a 40 % increase in anthropogenic emissions since 1980. Observed atmospheric N2O concentrations in recent years have exceeded the worst-case climate scenario, underscoring the importance of reducing anthropogenic N2O emissions.
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Nitrous oxide (N2O) is an important greenhouse gas. However, N2O emissions from estuaries underlie significant uncertainties due to limited data availability and high spatiotemporal variability. We found the Elbe Estuary (Germany) to be a year-round source of N2O, with the highest emissions in winter along with high nitrogen loads. However, in spring and summer, N2O emissions did not decrease alongside lower nitrogen loads because organic matter fueled in situ N2O production along the estuary.
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Damian L. Arévalo-Martínez, Amir Haroon, Hermann W. Bange, Ercan Erkul, Marion Jegen, Nils Moosdorf, Jens Schneider von Deimling, Christian Berndt, Michael Ernst Böttcher, Jasper Hoffmann, Volker Liebetrau, Ulf Mallast, Gudrun Massmann, Aaron Micallef, Holly A. Michael, Hendrik Paasche, Wolfgang Rabbel, Isaac Santos, Jan Scholten, Katrin Schwalenberg, Beata Szymczycha, Ariel T. Thomas, Joonas J. Virtasalo, Hannelore Waska, and Bradley A. Weymer
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Yanan Zhao, Dennis Booge, Christa A. Marandino, Cathleen Schlundt, Astrid Bracher, Elliot L. Atlas, Jonathan Williams, and Hermann W. Bange
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Wangwang Ye, Hermann W. Bange, Damian L. Arévalo-Martínez, Hailun He, Yuhong Li, Jianwen Wen, Jiexia Zhang, Jian Liu, Man Wu, and Liyang Zhan
Biogeosciences Discuss., https://doi.org/10.5194/bg-2021-334, https://doi.org/10.5194/bg-2021-334, 2022
Manuscript not accepted for further review
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CH4 is the second important greenhouse gas after CO2. We show that CH4 consumption and sea-ice melting influence the CH4 distribution in the Ross Sea (Southern Ocean), causing undersaturation and net uptake of CH4 during summertime. This study confirms the capability of surface water in the high-latitude Southern Ocean regions to take up atmospheric CH4 which, in turn, will help to improve predictions of how CH4 release/uptake from the ocean will develop when sea-ice retreats in the future.
Yanan Zhao, Cathleen Schlundt, Dennis Booge, and Hermann W. Bange
Biogeosciences, 18, 2161–2179, https://doi.org/10.5194/bg-18-2161-2021, https://doi.org/10.5194/bg-18-2161-2021, 2021
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Samuel T. Wilson, Alia N. Al-Haj, Annie Bourbonnais, Claudia Frey, Robinson W. Fulweiler, John D. Kessler, Hannah K. Marchant, Jana Milucka, Nicholas E. Ray, Parvadha Suntharalingam, Brett F. Thornton, Robert C. Upstill-Goddard, Thomas S. Weber, Damian L. Arévalo-Martínez, Hermann W. Bange, Heather M. Benway, Daniele Bianchi, Alberto V. Borges, Bonnie X. Chang, Patrick M. Crill, Daniela A. del Valle, Laura Farías, Samantha B. Joye, Annette Kock, Jabrane Labidi, Cara C. Manning, John W. Pohlman, Gregor Rehder, Katy J. Sparrow, Philippe D. Tortell, Tina Treude, David L. Valentine, Bess B. Ward, Simon Yang, and Leonid N. Yurganov
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Short summary
Our research is the first to measure dissolved NO concentrations in temperate estuarine waters, providing insights into its distribution under varying conditions and enhancing our understanding of its production processes. Dissolved NO was supersaturated in the Elbe Estuary, indicating that it is a source of atmospheric NO. The observed distribution of dissolved NO most likely resulted from nitrification.
Our research is the first to measure dissolved NO concentrations in temperate estuarine waters,...
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