13
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Marine iodine emissions in a changing world

      review-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Iodine is a critical trace element involved in many diverse and important processes in the Earth system. The importance of iodine for human health has been known for over a century, with low iodine in the diet being linked to goitre, cretinism and neonatal death. Research over the last few decades has shown that iodine has significant impacts on tropospheric photochemistry, ultimately impacting climate by reducing the radiative forcing of ozone (O 3) and air quality by reducing extreme O 3 concentrations in polluted regions. Iodine is naturally present in the ocean, predominantly as aqueous iodide and iodate. The rapid reaction of sea-surface iodide with O 3 is believed to be the largest single source of gaseous iodine to the atmosphere. Due to increased anthropogenic O 3, this release of iodine is believed to have increased dramatically over the twentieth century, by as much as a factor of 3. Uncertainties in the marine iodine distribution and global cycle are, however, major constraints in the effective prediction of how the emissions of iodine and its biogeochemical cycle may change in the future or have changed in the past. Here, we present a synthesis of recent results by our team and others which bring a fresh perspective to understanding the global iodine biogeochemical cycle. In particular, we suggest that future climate-induced oceanographic changes could result in a significant change in aqueous iodide concentrations in the surface ocean, with implications for atmospheric air quality and climate.

          Related collections

          Most cited references82

          • Record: found
          • Abstract: not found
          • Article: not found

          Atmospheric chemistry of iodine.

            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            The significance of nitrification for oceanic new production.

            The flux of organic material sinking to depth is a major control on the inventory of carbon in the ocean. To first order, the oceanic system is at equilibrium such that what goes down must come up. Because the export flux is difficult to measure directly, it is routinely estimated indirectly by quantifying the amount of phytoplankton growth, or primary production, fuelled by the upward flux of nitrate. To do so it is necessary to take into account other sources of biologically available nitrogen. However, the generation of nitrate by nitrification in surface waters has only recently received attention. Here we perform the first synthesis of open-ocean measurements of the specific rate of surface nitrification and use these to configure a global biogeochemical model to quantify the global role of nitrification. We show that for much of the world ocean a substantial fraction of the nitrate taken up is generated through recent nitrification near the surface. At the global scale, nitrification accounts for about half of the nitrate consumed by growing phytoplankton. A consequence is that many previous attempts to quantify marine carbon export, particularly those based on inappropriate use of the f-ratio (a measure of the efficiency of the 'biological pump'), are significant overestimates.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Global declines in oceanic nitrification rates as a consequence of ocean acidification.

              Ocean acidification produced by dissolution of anthropogenic carbon dioxide (CO(2)) emissions in seawater has profound consequences for marine ecology and biogeochemistry. The oceans have absorbed one-third of CO(2) emissions over the past two centuries, altering ocean chemistry, reducing seawater pH, and affecting marine animals and phytoplankton in multiple ways. Microbially mediated ocean biogeochemical processes will be pivotal in determining how the earth system responds to global environmental change; however, how they may be altered by ocean acidification is largely unknown. We show here that microbial nitrification rates decreased in every instance when pH was experimentally reduced (by 0.05-0.14) at multiple locations in the Atlantic and Pacific Oceans. Nitrification is a central process in the nitrogen cycle that produces both the greenhouse gas nitrous oxide and oxidized forms of nitrogen used by phytoplankton and other microorganisms in the sea; at the Bermuda Atlantic Time Series and Hawaii Ocean Time-series sites, experimental acidification decreased ammonia oxidation rates by 38% and 36%. Ammonia oxidation rates were also strongly and inversely correlated with pH along a gradient produced in the oligotrophic Sargasso Sea (r(2) = 0.87, P < 0.05). Across all experiments, rates declined by 8-38% in low pH treatments, and the greatest absolute decrease occurred where rates were highest off the California coast. Collectively our results suggest that ocean acidification could reduce nitrification rates by 3-44% within the next few decades, affecting oceanic nitrous oxide production, reducing supplies of oxidized nitrogen in the upper layers of the ocean, and fundamentally altering nitrogen cycling in the sea.
                Bookmark

                Author and article information

                Contributors
                Journal
                Proc Math Phys Eng Sci
                Proc Math Phys Eng Sci
                RSPA
                royprsa
                Proceedings. Mathematical, Physical, and Engineering Sciences
                The Royal Society Publishing
                1364-5021
                1471-2946
                March 2021
                March 3, 2021
                March 3, 2021
                : 477
                : 2247
                : 20200824
                Affiliations
                [ 1 ] Wolfson Atmospheric Chemistry Laboratories, Department of Chemistry, University of York, , York, UK
                [ 2 ] National Centre for Atmospheric Science (NCAS), University of York, , York YO10 5DD, UK
                [ 3 ] School of Chemistry, University of Leicester, , Leicester, UK
                [ 4 ] Department of Environment and Geography, University of York, , Wentworth Way, Heslington, York, UK
                [ 5 ] Centre for Ocean and Atmospheric Sciences, School of Environmental Sciences, University of East Anglia, , Norwich Research Park, Norwich, UK
                [ 6 ] Centre for Ocean and Atmospheric Sciences, School of Mathematics, University of East Anglia, , Norwich Research Park, Norwich, UK
                [ 7 ] Indian Institute of Tropical Meteorology, Ministry of Earth Sciences, , Pune 411008, India
                Author notes
                [ † ]

                Present address: Ricardo Energy and Environment, Harwell, Oxfordshire, UK.

                [ ‡ ]

                Present address: IMT Lille Douai, University of Lille, CERI EE - Sciences de L'Atmosphère et Génie de L'Environnement, 59000 Lille, France.

                An invited perspective to mark the election of Lucy Carpenter as a Fellow of the Royal Society in 2019.

                Author information
                http://orcid.org/0000-0002-6257-3950
                http://orcid.org/0000-0002-5906-176X
                http://orcid.org/0000-0002-3006-3876
                http://orcid.org/0000-0002-5756-4718
                http://orcid.org/0000-0003-4775-032X
                http://orcid.org/0000-0003-1742-2755
                Article
                rspa20200824
                10.1098/rspa.2020.0824
                8300602
                35153549
                ca653532-1dbd-4520-b7d5-190224eecda1
                © 2021 The Authors.

                Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.

                History
                : October 12, 2020
                : January 28, 2021
                Funding
                Funded by: H2020 European Research Council, http://dx.doi.org/10.13039/100010663;
                Award ID: 833290
                Funded by: Natural Environment Research Council (NERC);
                Award ID: NE/N009444/1
                Award ID: NE/N009983/1
                Award ID: NE/N01054X/1
                Categories
                1002
                1005
                11
                67
                140
                Perspective
                Perspective
                Custom metadata
                March 31, 2021

                Physics
                iodine,iodide,halogens,sea–air interactions,ozone,global iodine cycle
                Physics
                iodine, iodide, halogens, sea–air interactions, ozone, global iodine cycle

                Comments

                Comment on this article