Articles | Volume 19, issue 20
https://doi.org/10.5194/bg-19-5021-2022
© Author(s) 2022. 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-19-5021-2022
© Author(s) 2022. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Research article
| 
28 Oct 2022
Research article |
| 28 Oct 2022
| 28 Oct 2022
Winter season Southern Ocean distributions of climate-relevant trace gases
Li Zhou
CORRESPONDING AUTHOR
Research Division 2: Marine Biogeochemistry, GEOMAR Helmholtz Centre for Ocean Research Kiel, Kiel, Germany
Dennis Booge
Research Division 2: Marine Biogeochemistry, GEOMAR Helmholtz Centre for Ocean Research Kiel, Kiel, Germany
Key Laboratory of Global Change and Marine-Atmospheric Chemistry,Third Institute of Oceanography, Ministry of Natural Resources (MNR), Xiamen, PR China
Christa A. Marandino
Research Division 2: Marine Biogeochemistry, GEOMAR Helmholtz Centre for Ocean Research Kiel, Kiel, Germany
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Sankirna D. Joge, Anoop S. Mahajan, Shrivardhan Hulswar, Christa A. Marandino, Martí Galí, Thomas G. Bell, and Rafel Simó
Biogeosciences, 21, 4439–4452, https://doi.org/10.5194/bg-21-4439-2024, https://doi.org/10.5194/bg-21-4439-2024, 2024
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Dimethyl sulfide (DMS) is the largest natural source of sulfur in the atmosphere and leads to the formation of cloud condensation nuclei. DMS emission and quantification of its impacts have large uncertainties, but a detailed study on the emissions and drivers of their uncertainty is missing to date. The emissions are usually calculated from the seawater DMS concentrations and a flux parameterization. Here we quantify the differences in DMS seawater products, which can affect DMS fluxes.
Sankirna D. Joge, Anoop S. Mahajan, Shrivardhan Hulswar, Christa A. Marandino, Martí Galí, Thomas G. Bell, Mingxi Yang, and Rafel Simó
Biogeosciences, 21, 4453–4467, https://doi.org/10.5194/bg-21-4453-2024, https://doi.org/10.5194/bg-21-4453-2024, 2024
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Dimethyl sulfide (DMS) is the largest natural source of sulfur in the atmosphere and leads to the formation of cloud condensation nuclei. DMS emissions and quantification of their impacts have large uncertainties, but a detailed study on the range of emissions and drivers of their uncertainty is missing to date. The emissions are calculated from the seawater DMS concentrations and a flux parameterization. Here we quantify the differences in the effect of flux parameterizations used in models.
Dennis Booge, Jerry F. Tjiputra, Dirk J. L. Olivié, Birgit Quack, and Kirstin Krüger
Earth Syst. Dynam., 15, 801–816, https://doi.org/10.5194/esd-15-801-2024, https://doi.org/10.5194/esd-15-801-2024, 2024
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Oceanic bromoform, produced by algae, is an important precursor of atmospheric bromine, highlighting the importance of implementing these emissions in climate models. The simulated mean oceanic concentrations align well with observations, while the mean atmospheric values are lower than the observed ones. Modelled annual mean emissions mostly occur from the sea to the air and are driven by oceanic concentrations, sea surface temperature, and wind speed, which depend on season and location.
Jun Shi, Jinpei Yan, Shanshan Wang, Shuhui Zhao, Miming Zhang, Suqing Xu, Qi Lin, Hang Yang, and Siying Dai
Atmos. Chem. Phys., 23, 10349–10359, https://doi.org/10.5194/acp-23-10349-2023, https://doi.org/10.5194/acp-23-10349-2023, 2023
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An underway aerosol-monitoring system was used to determine the Na+ concentration during different cyclone periods in the Southern Ocean in order to assess the potential effects of cyclones on sea spray aerosol (SSA) emissions. It was estimated that more than 23 % of SSAs were transported upwards during cyclone periods. Vertically transported SSAs can be regarded as an important source of CCN and hence have an effect on climate in the middle and high latitudes of the Southern Hemisphere.
Sonja Gindorf, Hermann W. Bange, Dennis Booge, and Annette Kock
Biogeosciences, 19, 4993–5006, https://doi.org/10.5194/bg-19-4993-2022, https://doi.org/10.5194/bg-19-4993-2022, 2022
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Methane is a climate-relevant greenhouse gas which is emitted to the atmosphere from coastal areas such as the Baltic Sea. We measured the methane concentration in the water column of the western Kiel Bight. Methane concentrations were higher in September than in June. We found no relationship between the 2018 European heatwave and methane concentrations. Our results show that the methane distribution in the water column is strongly affected by temporal and spatial variabilities.
Miming Zhang, Jinpei Yan, Qi Lin, Hongguo Zheng, Keyhong Park, Shuhui Zhao, Suqing Xu, Meina Ruan, Shanshan Wang, Xinlin Zhong, and Suli Zhao
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2022-454, https://doi.org/10.5194/acp-2022-454, 2022
Revised manuscript not accepted
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Extremely low contribution of DMS chemistry to the aerosols over the high AO was determined by the inhibition of marine phytoplankton, which extends the knowledge how will biogenic sulfur cycle impact the regional climate as AO sea ice retreat in the future.
Susann Tegtmeier, Christa Marandino, Yue Jia, Birgit Quack, and Anoop S. Mahajan
Atmos. Chem. Phys., 22, 6625–6676, https://doi.org/10.5194/acp-22-6625-2022, https://doi.org/10.5194/acp-22-6625-2022, 2022
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In the atmosphere over the Indian Ocean, intense anthropogenic pollution from Southeast Asia mixes with pristine oceanic air. During the winter monsoon, high pollution levels are regularly observed over the entire northern Indian Ocean, while during the summer monsoon, clean air dominates. Here, we review current progress in detecting and understanding atmospheric gas-phase composition over the Indian Ocean and its impacts on the upper atmosphere, oceanic biogeochemistry, and marine ecosystems.
Yanan Zhao, Dennis Booge, Christa A. Marandino, Cathleen Schlundt, Astrid Bracher, Elliot L. Atlas, Jonathan Williams, and Hermann W. Bange
Biogeosciences, 19, 701–714, https://doi.org/10.5194/bg-19-701-2022, https://doi.org/10.5194/bg-19-701-2022, 2022
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We present here, for the first time, simultaneously measured dimethylsulfide (DMS) seawater concentrations and DMS atmospheric mole fractions from the Peruvian upwelling region during two cruises in December 2012 and October 2015. Our results indicate low oceanic DMS concentrations and atmospheric DMS molar fractions in surface waters and the atmosphere, respectively. In addition, the Peruvian upwelling region was identified as an insignificant source of DMS emissions during both periods.
Sinikka T. Lennartz, Michael Gauss, Marc von Hobe, and Christa A. Marandino
Earth Syst. Sci. Data, 13, 2095–2110, https://doi.org/10.5194/essd-13-2095-2021, https://doi.org/10.5194/essd-13-2095-2021, 2021
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This study provides a marine emission inventory for the sulphur gases carbonyl sulphide (OCS) and carbon disulphide (CS2), derived from a numerical model of the surface ocean at monthly resolution for the period 2000–2019. Comparison with a database of seaborne observations reveals very good agreement for OCS. Interannual variability in both gases seems to be mainly driven by the amount of chromophoric dissolved organic matter present in surface water.
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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We present a unique and comprehensive time-series study of biogenic sulfur compounds in the southwestern Baltic Sea, from 2009 to 2018. Dimethyl sulfide is one of the key players regulating global climate change, as well as dimethylsulfoniopropionate and dimethyl sulfoxide. Their decadal trends did not follow increasing temperature but followed some algae group abundances at the Boknis Eck Time Series Station.
Jinpei Yan, Jinyoung Jung, Miming Zhang, Federico Bianchi, Yee Jun Tham, Suqing Xu, Qi Lin, Shuhui Zhao, Lei Li, and Liqi Chen
Atmos. Chem. Phys., 20, 3259–3271, https://doi.org/10.5194/acp-20-3259-2020, https://doi.org/10.5194/acp-20-3259-2020, 2020
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Methanesulfonic acid (MSA) is important to the CCN in the MBL. The uptake of MSA on particles is lacking in knowledge. The characteristics of MSA uptake on different particles were studied in the Southern Ocean. The MSA uptake on different particles was associated with particle properties. Uptake of MSA on sea salt particles was favored, while acidic and hydrophobic particles suppressed the MSA uptake. The results extend the knowledge of MSA formation and behavior in the atmosphere.
Sinikka T. Lennartz, Christa A. Marandino, Marc von Hobe, Meinrat O. Andreae, Kazushi Aranami, Elliot Atlas, Max Berkelhammer, Heinz Bingemer, Dennis Booge, Gregory Cutter, Pau Cortes, Stefanie Kremser, Cliff S. Law, Andrew Marriner, Rafel Simó, Birgit Quack, Günther Uher, Huixiang Xie, and Xiaobin Xu
Earth Syst. Sci. Data, 12, 591–609, https://doi.org/10.5194/essd-12-591-2020, https://doi.org/10.5194/essd-12-591-2020, 2020
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Sulfur-containing trace gases in the atmosphere influence atmospheric chemistry and the energy budget of the Earth by forming aerosols. The ocean is an important source of the most abundant sulfur gas in the atmosphere, carbonyl sulfide (OCS) and its most important precursor carbon disulfide (CS2). In order to assess global variability of the sea surface concentrations of both gases to calculate their oceanic emissions, we have compiled a database of existing shipborne measurements.
Sinikka T. Lennartz, Marc von Hobe, Dennis Booge, Henry C. Bittig, Tim Fischer, Rafael Gonçalves-Araujo, Kerstin B. Ksionzek, Boris P. Koch, Astrid Bracher, Rüdiger Röttgers, Birgit Quack, and Christa A. Marandino
Ocean Sci., 15, 1071–1090, https://doi.org/10.5194/os-15-1071-2019, https://doi.org/10.5194/os-15-1071-2019, 2019
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The ocean emits the gases carbonyl sulfide (OCS) and carbon disulfide (CS2), which affect our climate. The goal of this study was to quantify the rates at which both gases are produced in the eastern tropical South Pacific (ETSP), one of the most productive oceanic regions worldwide. Both gases are produced by reactions triggered by sunlight, but we found that the amount produced depends on different factors. Our results improve numerical models to predict oceanic concentrations of both gases.
Alexander Zavarsky and Christa A. Marandino
Atmos. Chem. Phys., 19, 1819–1834, https://doi.org/10.5194/acp-19-1819-2019, https://doi.org/10.5194/acp-19-1819-2019, 2019
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Wind–wave interaction can suppress gas transfer between the atmosphere and the ocean. Using a global wave model we investigate the impact of this interaction on the global gas transfer of CO2 and DMS. We also investigate the impact on of gas transfer limitation on two commonly used gas transfer velocity parameterizations.
Dennis Booge, Cathleen Schlundt, Astrid Bracher, Sonja Endres, Birthe Zäncker, and Christa A. Marandino
Biogeosciences, 15, 649–667, https://doi.org/10.5194/bg-15-649-2018, https://doi.org/10.5194/bg-15-649-2018, 2018
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Our isoprene data from field measurements in the mixed layer from the Indian Ocean and the eastern Pacific Ocean show that the ability of different phytoplankton functional types to produce isoprene seems to be mainly influenced by light, ocean temperature, salinity, and nutrients. By calculating in-field isoprene production rates, we demonstrate that an additional loss is needed to explain the measured isoprene concentration, which is potentially due to degradation or consumption by bacteria.
Cathleen Schlundt, Susann Tegtmeier, Sinikka T. Lennartz, Astrid Bracher, Wee Cheah, Kirstin Krüger, Birgit Quack, and Christa A. Marandino
Atmos. Chem. Phys., 17, 10837–10854, https://doi.org/10.5194/acp-17-10837-2017, https://doi.org/10.5194/acp-17-10837-2017, 2017
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For the first time, oxygenated volatile organic carbon (OVOC) in the ocean and overlaying atmosphere in the western Pacific Ocean has been measured. OVOCs are important for atmospheric chemistry. They are involved in ozone production in the upper troposphere (UT), and they have a climate cooling effect. We showed that phytoplankton was an important source for OVOCs in the surface ocean, and when OVOCs are emitted into the atmosphere, they could reach the UT and might influence ozone formation.
Sinikka T. Lennartz, Christa A. Marandino, Marc von Hobe, Pau Cortes, Birgit Quack, Rafel Simo, Dennis Booge, Andrea Pozzer, Tobias Steinhoff, Damian L. Arevalo-Martinez, Corinna Kloss, Astrid Bracher, Rüdiger Röttgers, Elliot Atlas, and Kirstin Krüger
Atmos. Chem. Phys., 17, 385–402, https://doi.org/10.5194/acp-17-385-2017, https://doi.org/10.5194/acp-17-385-2017, 2017
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We present new sea surface and marine boundary layer measurements of carbonyl sulfide, the most abundant sulfur gas in the atmosphere, and calculate an oceanic emission estimate. Our results imply that oceanic emissions are very unlikely to account for the missing source in the atmospheric budget that is currently discussed for OCS.
Dennis Booge, Christa A. Marandino, Cathleen Schlundt, Paul I. Palmer, Michael Schlundt, Elliot L. Atlas, Astrid Bracher, Eric S. Saltzman, and Douglas W. R. Wallace
Atmos. Chem. Phys., 16, 11807–11821, https://doi.org/10.5194/acp-16-11807-2016, https://doi.org/10.5194/acp-16-11807-2016, 2016
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Isoprene, a biogenic trace gas, is an important precursor of secondary organic aerosol/cloud condensation nuclei. Here, we use isoprene and related field measurements from three different ocean data sets together with remotely sensed satellite data to model global marine isoprene emissions. Our findings suggest that there is at least one missing oceanic source of isoprene and possibly other unknown factors in the ocean or atmosphere influencing the atmospheric values.
Lothar Stramma, Tim Fischer, Damian S. Grundle, Gerd Krahmann, Hermann W. Bange, and Christa A. Marandino
Ocean Sci., 12, 861–873, https://doi.org/10.5194/os-12-861-2016, https://doi.org/10.5194/os-12-861-2016, 2016
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Results from a research cruise on R/V Sonne to the eastern tropical Pacific in October 2015 during the 2015–2016 El Niño show the transition of current, hydrographic, and nutrient conditions to El Niño conditions in the eastern tropical Pacific in October 2015. Although in early 2015 the El Niño was strong and in October 2015 showed a clear El Niño influence on the EUC, in the eastern tropical Pacific the measurements only showed developing El Niño water mass distributions.
S. T. Lennartz, G. Krysztofiak, C. A. Marandino, B.-M. Sinnhuber, S. Tegtmeier, F. Ziska, R. Hossaini, K. Krüger, S. A. Montzka, E. Atlas, D. E. Oram, T. Keber, H. Bönisch, and B. Quack
Atmos. Chem. Phys., 15, 11753–11772, https://doi.org/10.5194/acp-15-11753-2015, https://doi.org/10.5194/acp-15-11753-2015, 2015
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Marine-produced short-lived trace gases such as halocarbons and DMS significantly impact atmospheric chemistry. To assess this impact on ozone depletion and the radiative budget, it is critical that their marine emissions in atmospheric chemistry models are quantified as accurately as possible. We show that calculating emissions online with an interactive atmosphere improves the agreement with current observations and should be employed regularly in models where marine sources are important.
T. G. Bell, W. De Bruyn, C. A. Marandino, S. D. Miller, C. S. Law, M. J. Smith, and E. S. Saltzman
Atmos. Chem. Phys., 15, 1783–1794, https://doi.org/10.5194/acp-15-1783-2015, https://doi.org/10.5194/acp-15-1783-2015, 2015
C. A. Marandino, S. Tegtmeier, K. Krüger, C. Zindler, E. L. Atlas, F. Moore, and H. W. Bange
Atmos. Chem. Phys., 13, 8427–8437, https://doi.org/10.5194/acp-13-8427-2013, https://doi.org/10.5194/acp-13-8427-2013, 2013
C. Zindler, A. Bracher, C. A. Marandino, B. Taylor, E. Torrecilla, A. Kock, and H. W. Bange
Biogeosciences, 10, 3297–3311, https://doi.org/10.5194/bg-10-3297-2013, https://doi.org/10.5194/bg-10-3297-2013, 2013
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Biogeochemistry: Air - Sea Exchange
Dimethyl sulfide (DMS) climatologies, fluxes, and trends – Part 1: Differences between seawater DMS estimations
Dimethyl sulfide (DMS) climatologies, fluxes, and trends – Part 2: Sea–air fluxes
High-frequency continuous measurements reveal strong diel and seasonal cycling of pCO2 and CO2 flux in a mesohaline reach of the Chesapeake Bay
Significant role of physical transport in the marine carbon monoxide (CO) cycle: observations in the East Sea (Sea of Japan), the western North Pacific, and the Bering Sea in summer
Central Arctic Ocean surface–atmosphere exchange of CO2 and CH4 constrained by direct measurements
Spatial and seasonal variability in volatile organic sulfur compounds in seawater and the overlying atmosphere of the Bohai and Yellow seas
Estimating marine carbon uptake in the northeast Pacific using a neural network approach
Sea–air methane flux estimates derived from marine surface observations and instantaneous atmospheric measurements in the northern Labrador Sea and Baffin Bay
Global analysis of the controls on seawater dimethylsulfide spatial variability
Air–sea gas exchange in a seagrass ecosystem – results from a 3He ∕ SF6 tracer release experiment
Concentrations of dissolved dimethyl sulfide (DMS), methanethiol and other trace gases in context of microbial communities from the temperate Atlantic to the Arctic Ocean
Marine nitrogen fixation as a possible source of atmospheric water-soluble organic nitrogen aerosols in the subtropical North Pacific
Ice nucleating properties of the sea ice diatom Fragilariopsis cylindrus and its exudates
On physical mechanisms enhancing air–sea CO2 exchange
How biogenic polymers control surfactant dynamics in the surface microlayer: insights from a coastal Baltic Sea study
Identifying the biological control of the annual and multi-year variations in South Atlantic air–sea CO2 flux
The sensitivity of pCO2 reconstructions to sampling scales across a Southern Ocean sub-domain: a semi-idealized ocean sampling simulation approach
Physical mechanisms for biological carbon uptake during the onset of the spring phytoplankton bloom in the northwestern Mediterranean Sea (BOUSSOLE site)
Wintertime process study of the North Brazil Current rings reveals the region as a larger sink for CO2 than expected
New constraints on biological production and mixing processes in the South China Sea from triple isotope composition of dissolved oxygen
Tidal mixing of estuarine and coastal waters in the western English Channel is a control on spatial and temporal variability in seawater CO2
A seamless ensemble-based reconstruction of surface ocean pCO2 and air–sea CO2 fluxes over the global coastal and open oceans
Sea ice concentration impacts dissolved organic gases in the Canadian Arctic
Evaluating the Arabian Sea as a regional source of atmospheric CO2: seasonal variability and drivers
An empirical MLR for estimating surface layer DIC and a comparative assessment to other gap-filling techniques for ocean carbon time series
Derivation of seawater pCO2 from net community production identifies the South Atlantic Ocean as a CO2 source
Eukaryotic community composition in the sea surface microlayer across an east–west transect in the Mediterranean Sea
Enhancement of the North Atlantic CO2 sink by Arctic Waters
Global ocean dimethyl sulfide climatology estimated from observations and an artificial neural network
Atmospheric deposition of organic matter at a remote site in the central Mediterranean Sea: implications for the marine ecosystem
Underway seawater and atmospheric measurements of volatile organic compounds in the Southern Ocean
Dimethylsulfide (DMS), marine biogenic aerosols and the ecophysiology of coral reefs
Spatial variations in CO2 fluxes in the Saguenay Fjord (Quebec, Canada) and results of a water mixing model
Gas exchange estimates in the Peruvian upwelling regime biased by multi-day near-surface stratification
Insights from year-long measurements of air–water CH4 and CO2 exchange in a coastal environment
On the role of climate modes in modulating the air–sea CO2 fluxes in eastern boundary upwelling systems
Reviews and syntheses: the GESAMP atmospheric iron deposition model intercomparison study
Increase of dissolved inorganic carbon and decrease in pH in near-surface waters in the Mediterranean Sea during the past two decades
Utilizing the Drake Passage Time-series to understand variability and change in subpolar Southern Ocean pCO2
Effect of wind speed on the size distribution of gel particles in the sea surface microlayer: insights from a wind–wave channel experiment
The seasonal cycle of pCO2 and CO2 fluxes in the Southern Ocean: diagnosing anomalies in CMIP5 Earth system models
Marine phytoplankton stoichiometry mediates nonlinear interactions between nutrient supply, temperature, and atmospheric CO2
Interannual drivers of the seasonal cycle of CO2 in the Southern Ocean
Constraints on global oceanic emissions of N2O from observations and models
Arctic Ocean CO2 uptake: an improved multiyear estimate of the air–sea CO2 flux incorporating chlorophyll a concentrations
Uncertainty in the global oceanic CO2 uptake induced by wind forcing: quantification and spatial analysis
Phytoplankton growth response to Asian dust addition in the northwest Pacific Ocean versus the Yellow Sea
Global high-resolution monthly pCO2 climatology for the coastal ocean derived from neural network interpolation
Changes in the partial pressure of carbon dioxide in the Mauritanian–Cap Vert upwelling region between 2005 and 2012
Impact of ocean acidification on Arctic phytoplankton blooms and dimethyl sulfide concentration under simulated ice-free and under-ice conditions
Sankirna D. Joge, Anoop S. Mahajan, Shrivardhan Hulswar, Christa A. Marandino, Martí Galí, Thomas G. Bell, and Rafel Simó
Biogeosciences, 21, 4439–4452, https://doi.org/10.5194/bg-21-4439-2024, https://doi.org/10.5194/bg-21-4439-2024, 2024
Short summary
Short summary
Dimethyl sulfide (DMS) is the largest natural source of sulfur in the atmosphere and leads to the formation of cloud condensation nuclei. DMS emission and quantification of its impacts have large uncertainties, but a detailed study on the emissions and drivers of their uncertainty is missing to date. The emissions are usually calculated from the seawater DMS concentrations and a flux parameterization. Here we quantify the differences in DMS seawater products, which can affect DMS fluxes.
Sankirna D. Joge, Anoop S. Mahajan, Shrivardhan Hulswar, Christa A. Marandino, Martí Galí, Thomas G. Bell, Mingxi Yang, and Rafel Simó
Biogeosciences, 21, 4453–4467, https://doi.org/10.5194/bg-21-4453-2024, https://doi.org/10.5194/bg-21-4453-2024, 2024
Short summary
Short summary
Dimethyl sulfide (DMS) is the largest natural source of sulfur in the atmosphere and leads to the formation of cloud condensation nuclei. DMS emissions and quantification of their impacts have large uncertainties, but a detailed study on the range of emissions and drivers of their uncertainty is missing to date. The emissions are calculated from the seawater DMS concentrations and a flux parameterization. Here we quantify the differences in the effect of flux parameterizations used in models.
A. Whitman Miller, Jim R. Muirhead, Amanda C. Reynolds, Mark S. Minton, and Karl J. Klug
Biogeosciences, 21, 3717–3734, https://doi.org/10.5194/bg-21-3717-2024, https://doi.org/10.5194/bg-21-3717-2024, 2024
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High frequency pCO2 measurements reveal net neutral CO2 flux in a mesohaline reach of the Chesapeake Bay. Net off-gassing to the atmosphere begins in June when water temperatures rise above ~26ºC, continuing through November when temperatures fall below ~10ºC. Dissolved CO2 concentrations follow day–night cycles and are especially pronounced in warm waters. From December through May, the river is largely an uninterrupted sink for CO2 (i.e. CO2 is drawn out of the atmosphere into the river).
Young Shin Kwon, Tae Siek Rhee, Hyun-Cheol Kim, and Hyoun-Woo Kang
Biogeosciences, 21, 1847–1865, https://doi.org/10.5194/bg-21-1847-2024, https://doi.org/10.5194/bg-21-1847-2024, 2024
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Delving into CO dynamics from the East Sea to the Bering Sea, our study unveils the influence of physical transport on CO budgets. By measuring CO concentrations and parameters, we elucidate the interplay between biological and physical processes, highlighting the role of lateral transport in shaping CO distributions. Our findings underscore the importance of considering both biogeochemical and physical drivers in understanding marine carbon fluxes.
John Prytherch, Sonja Murto, Ian Brown, Adam Ulfsbo, Brett F. Thornton, Volker Brüchert, Michael Tjernström, Anna Lunde Hermansson, Amanda T. Nylund, and Lina A. Holthusen
Biogeosciences, 21, 671–688, https://doi.org/10.5194/bg-21-671-2024, https://doi.org/10.5194/bg-21-671-2024, 2024
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We directly measured methane and carbon dioxide exchange between ocean or sea ice and the atmosphere during an icebreaker-based expedition to the central Arctic Ocean (CAO) in summer 2021. These measurements can help constrain climate models and carbon budgets. The methane measurements, the first such made in the CAO, are lower than previous estimates and imply that the CAO is an insignificant contributor to Arctic methane emission. Gas exchange rates are slower than previous estimates.
Juan Yu, Lei Yu, Zhen He, Gui-Peng Yang, Jing-Guang Lai, and Qian Liu
Biogeosciences, 21, 161–176, https://doi.org/10.5194/bg-21-161-2024, https://doi.org/10.5194/bg-21-161-2024, 2024
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The distributions of volatile organic sulfur compounds (VSCs) (DMS, COS, and CS2) in the seawater and atmosphere of the Bohai and Yellow Seas were evaluated. Seasonal variations in VSCs were found and showed summer > spring. The COS concentrations exhibited positive correlation with DOC concentrations in seawater during summer. VSCs concentrations in seawater decreased with the depth. Sea-to-air fluxes of COS, DMS, and CS2 indicated that these marginal seas are sources of atmospheric VSCs.
Patrick J. Duke, Roberta C. Hamme, Debby Ianson, Peter Landschützer, Mohamed M. M. Ahmed, Neil C. Swart, and Paul A. Covert
Biogeosciences, 20, 3919–3941, https://doi.org/10.5194/bg-20-3919-2023, https://doi.org/10.5194/bg-20-3919-2023, 2023
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The ocean is both impacted by climate change and helps mitigate its effects through taking up carbon from the atmosphere. We used a machine learning approach to investigate what controls open-ocean carbon uptake in the northeast Pacific open ocean. Marine heatwaves that lasted 2–3 years increased uptake, while the upwelling strength of the Alaskan Gyre controlled uptake over 10-year time periods. The trend from 1998–2019 suggests carbon uptake in the northeast Pacific open ocean is increasing.
Judith Vogt, David Risk, Evelise Bourlon, Kumiko Azetsu-Scott, Evan N. Edinger, and Owen A. Sherwood
Biogeosciences, 20, 1773–1787, https://doi.org/10.5194/bg-20-1773-2023, https://doi.org/10.5194/bg-20-1773-2023, 2023
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The release of the greenhouse gas methane from Arctic submarine sources could exacerbate climate change in a positive feedback. Continuous monitoring of atmospheric methane levels over a 5100 km voyage in the western margin of the Labrador Sea and Baffin Bay revealed above-global averages likely affected by both onshore and offshore methane sources. Instantaneous sea–air methane fluxes were near zero at all measured stations, including a persistent cold-seep location.
George Manville, Thomas G. Bell, Jane P. Mulcahy, Rafel Simó, Martí Galí, Anoop S. Mahajan, Shrivardhan Hulswar, and Paul R. Halloran
Biogeosciences, 20, 1813–1828, https://doi.org/10.5194/bg-20-1813-2023, https://doi.org/10.5194/bg-20-1813-2023, 2023
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We present the first global investigation of controls on seawater dimethylsulfide (DMS) spatial variability over scales of up to 100 km. Sea surface height anomalies, density, and chlorophyll a help explain almost 80 % of DMS variability. The results suggest that physical and biogeochemical processes play an equally important role in controlling DMS variability. These data provide independent confirmation that existing parameterisations of seawater DMS concentration use appropriate variables.
Ryo Dobashi and David T. Ho
Biogeosciences, 20, 1075–1087, https://doi.org/10.5194/bg-20-1075-2023, https://doi.org/10.5194/bg-20-1075-2023, 2023
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Seagrass meadows are productive ecosystems and bury much carbon. Understanding their role in the global carbon cycle requires knowledge of air–sea CO2 fluxes and hence the knowledge of gas transfer velocity (k). In this study, k was determined from the dual tracer technique in Florida Bay. The observed gas transfer velocity was lower than previous studies in the coastal and open oceans at the same wind speeds, most likely due to wave attenuation by seagrass and limited wind fetch in this area.
Valérie Gros, Bernard Bonsang, Roland Sarda-Estève, Anna Nikolopoulos, Katja Metfies, Matthias Wietz, and Ilka Peeken
Biogeosciences, 20, 851–867, https://doi.org/10.5194/bg-20-851-2023, https://doi.org/10.5194/bg-20-851-2023, 2023
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The oceans are both sources and sinks for trace gases important for atmospheric chemistry and marine ecology. Here, we quantified selected trace gases (including the biological metabolites dissolved dimethyl sulfide, methanethiol and isoprene) along a 2500 km transect from the North Atlantic to the Arctic Ocean. In the context of phytoplankton and bacterial communities, our study suggests that methanethiol (rarely measured before) might substantially influence ocean–atmosphere cycling.
Tsukasa Dobashi, Yuzo Miyazaki, Eri Tachibana, Kazutaka Takahashi, Sachiko Horii, Fuminori Hashihama, Saori Yasui-Tamura, Yoko Iwamoto, Shu-Kuan Wong, and Koji Hamasaki
Biogeosciences, 20, 439–449, https://doi.org/10.5194/bg-20-439-2023, https://doi.org/10.5194/bg-20-439-2023, 2023
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Water-soluble organic nitrogen (WSON) in marine aerosols is important for biogeochemical cycling of bioelements. Our shipboard measurements suggested that reactive nitrogen produced and exuded by nitrogen-fixing microorganisms in surface seawater likely contributed to the formation of WSON aerosols in the subtropical North Pacific. This study provides new implications for the role of marine microbial activity in the formation of WSON aerosols in the ocean surface.
Lukas Eickhoff, Maddalena Bayer-Giraldi, Naama Reicher, Yinon Rudich, and Thomas Koop
Biogeosciences, 20, 1–14, https://doi.org/10.5194/bg-20-1-2023, https://doi.org/10.5194/bg-20-1-2023, 2023
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The formation of ice is an important process in Earth’s atmosphere, biosphere, and cryosphere, in particular in polar regions. Our research focuses on the influence of the sea ice diatom Fragilariopsis cylindrus and of molecules produced by it upon heterogenous ice nucleation. For that purpose, we studied the freezing of tiny droplets containing the diatoms in a microfluidic device. Together with previous studies, our results suggest a common freezing behaviour of various sea ice diatoms.
Lucía Gutiérrez-Loza, Erik Nilsson, Marcus B. Wallin, Erik Sahlée, and Anna Rutgersson
Biogeosciences, 19, 5645–5665, https://doi.org/10.5194/bg-19-5645-2022, https://doi.org/10.5194/bg-19-5645-2022, 2022
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The exchange of CO2 between the ocean and the atmosphere is an essential aspect of the global carbon cycle and is highly relevant for the Earth's climate. In this study, we used 9 years of in situ measurements to evaluate the temporal variability in the air–sea CO2 fluxes in the Baltic Sea. Furthermore, using this long record, we assessed the effect of atmospheric and water-side mechanisms controlling the efficiency of the air–sea CO2 exchange under different wind-speed conditions.
Theresa Barthelmeß and Anja Engel
Biogeosciences, 19, 4965–4992, https://doi.org/10.5194/bg-19-4965-2022, https://doi.org/10.5194/bg-19-4965-2022, 2022
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Greenhouse gases released by human activity cause a global rise in mean temperatures. While scientists can predict how much of these gases accumulate in the atmosphere based on not only human-derived sources but also oceanic sinks, it is rather difficult to predict the major influence of coastal ecosystems. We provide a detailed study on the occurrence, composition, and controls of substances that suppress gas exchange. We thus help to determine what controls coastal greenhouse gas fluxes.
Daniel J. Ford, Gavin H. Tilstone, Jamie D. Shutler, and Vassilis Kitidis
Biogeosciences, 19, 4287–4304, https://doi.org/10.5194/bg-19-4287-2022, https://doi.org/10.5194/bg-19-4287-2022, 2022
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This study explores the seasonal, inter-annual, and multi-year drivers of the South Atlantic air–sea CO2 flux. Our analysis showed seasonal sea surface temperatures dominate in the subtropics, and the subpolar regions correlated with biological processes. Inter-annually, the El Niño–Southern Oscillation correlated with the CO2 flux by modifying sea surface temperatures and biological activity. Long-term trends indicated an important biological contribution to changes in the air–sea CO2 flux.
Laique M. Djeutchouang, Nicolette Chang, Luke Gregor, Marcello Vichi, and Pedro M. S. Monteiro
Biogeosciences, 19, 4171–4195, https://doi.org/10.5194/bg-19-4171-2022, https://doi.org/10.5194/bg-19-4171-2022, 2022
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Based on observing system simulation experiments using a mesoscale-resolving model, we found that to significantly improve uncertainties and biases in carbon dioxide (CO2) mapping in the Southern Ocean, it is essential to resolve the seasonal cycle (SC) of the meridional gradient of CO2 through high frequency (at least daily) observations that also span the region's meridional axis. We also showed that the estimated SC anomaly and mean annual CO2 are highly sensitive to seasonal sampling biases.
Liliane Merlivat, Michael Hemming, Jacqueline Boutin, David Antoine, Vincenzo Vellucci, Melek Golbol, Gareth A. Lee, and Laurence Beaumont
Biogeosciences, 19, 3911–3920, https://doi.org/10.5194/bg-19-3911-2022, https://doi.org/10.5194/bg-19-3911-2022, 2022
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We use in situ high-temporal-resolution measurements of dissolved inorganic carbon and atmospheric parameters at the air–sea interface to analyse phytoplankton bloom initiation identified as the net rate of biological carbon uptake in the Mediterranean Sea. The shift from wind-driven to buoyancy-driven mixing creates conditions for blooms to begin. Active mixing at the air–sea interface leads to the onset of the surface phytoplankton bloom due to the relaxation of wind speed following storms.
Léa Olivier, Jacqueline Boutin, Gilles Reverdin, Nathalie Lefèvre, Peter Landschützer, Sabrina Speich, Johannes Karstensen, Matthieu Labaste, Christophe Noisel, Markus Ritschel, Tobias Steinhoff, and Rik Wanninkhof
Biogeosciences, 19, 2969–2988, https://doi.org/10.5194/bg-19-2969-2022, https://doi.org/10.5194/bg-19-2969-2022, 2022
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We investigate the impact of the interactions between eddies and the Amazon River plume on the CO2 air–sea fluxes to better characterize the ocean carbon sink in winter 2020. The region is a strong CO2 sink, previously underestimated by a factor of 10 due to a lack of data and understanding of the processes responsible for the variability in ocean carbon parameters. The CO2 absorption is mainly driven by freshwater from the Amazon entrained by eddies and by the winter seasonal cooling.
Hana Jurikova, Osamu Abe, Fuh-Kwo Shiah, and Mao-Chang Liang
Biogeosciences, 19, 2043–2058, https://doi.org/10.5194/bg-19-2043-2022, https://doi.org/10.5194/bg-19-2043-2022, 2022
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We studied the isotopic composition of oxygen dissolved in seawater in the South China Sea. This tells us about the origin of oxygen in the water column, distinguishing between biological oxygen produced by phytoplankton communities and atmospheric oxygen entering seawater through gas exchange. We found that the East Asian Monsoon plays an important role in determining the amount of oxygen produced vs. consumed by the phytoplankton, as well as in inducing vertical water mass mixing.
Richard P. Sims, Michael Bedington, Ute Schuster, Andrew J. Watson, Vassilis Kitidis, Ricardo Torres, Helen S. Findlay, James R. Fishwick, Ian Brown, and Thomas G. Bell
Biogeosciences, 19, 1657–1674, https://doi.org/10.5194/bg-19-1657-2022, https://doi.org/10.5194/bg-19-1657-2022, 2022
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The amount of carbon dioxide (CO2) being absorbed by the ocean is relevant to the earth's climate. CO2 values in the coastal ocean and estuaries are not well known because of the instrumentation used. We used a new approach to measure CO2 across the coastal and estuarine zone. We found that CO2 and salinity were linked to the state of the tide. We used our CO2 measurements and model salinity to predict CO2. Previous studies overestimate how much CO2 the coastal ocean draws down at our site.
Thi Tuyet Trang Chau, Marion Gehlen, and Frédéric Chevallier
Biogeosciences, 19, 1087–1109, https://doi.org/10.5194/bg-19-1087-2022, https://doi.org/10.5194/bg-19-1087-2022, 2022
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Air–sea CO2 fluxes and associated uncertainty over the open ocean to coastal shelves are estimated with a new ensemble-based reconstruction of pCO2 trained on observation-based data. The regional distribution and seasonality of CO2 sources and sinks are consistent with those suggested in previous studies as well as mechanisms discussed therein. The ensemble-based uncertainty field allows identifying critical regions where improvements in pCO2 and air–sea CO2 flux estimates should be a priority.
Charel Wohl, Anna E. Jones, William T. Sturges, Philip D. Nightingale, Brent Else, Brian J. Butterworth, and Mingxi Yang
Biogeosciences, 19, 1021–1045, https://doi.org/10.5194/bg-19-1021-2022, https://doi.org/10.5194/bg-19-1021-2022, 2022
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We measured concentrations of five different organic gases in seawater in the high Arctic during summer. We found higher concentrations near the surface of the water column (top 5–10 m) and in areas of partial ice cover. This suggests that sea ice influences the concentrations of these gases. These gases indirectly exert a slight cooling effect on the climate, and it is therefore important to measure the levels accurately for future climate predictions.
Alain de Verneil, Zouhair Lachkar, Shafer Smith, and Marina Lévy
Biogeosciences, 19, 907–929, https://doi.org/10.5194/bg-19-907-2022, https://doi.org/10.5194/bg-19-907-2022, 2022
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The Arabian Sea is a natural CO2 source to the atmosphere, but previous work highlights discrepancies between data and models in estimating air–sea CO2 flux. In this study, we use a regional ocean model, achieve a flux closer to available data, and break down the seasonal cycles that impact it, with one result being the great importance of monsoon winds. As demonstrated in a meta-analysis, differences from data still remain, highlighting the great need for further regional data collection.
Jesse M. Vance, Kim Currie, John Zeldis, Peter W. Dillingham, and Cliff S. Law
Biogeosciences, 19, 241–269, https://doi.org/10.5194/bg-19-241-2022, https://doi.org/10.5194/bg-19-241-2022, 2022
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Long-term monitoring is needed to detect changes in our environment. Time series of ocean carbon have aided our understanding of seasonal cycles and provided evidence for ocean acidification. Data gaps are inevitable, yet no standard method for filling gaps exists. We present a regression approach here and compare it to seven other common methods to understand the impact of different approaches when assessing seasonal to climatic variability in ocean carbon.
Daniel J. Ford, Gavin H. Tilstone, Jamie D. Shutler, and Vassilis Kitidis
Biogeosciences, 19, 93–115, https://doi.org/10.5194/bg-19-93-2022, https://doi.org/10.5194/bg-19-93-2022, 2022
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This study identifies the most accurate biological proxy for the estimation of seawater pCO2 fields, which are key to assessing the ocean carbon sink. Our analysis shows that the net community production (NCP), the balance between photosynthesis and respiration, was more accurate than chlorophyll a within a neural network scheme. The improved pCO2 estimates, based on NCP, identified the South Atlantic Ocean as a net CO2 source, compared to a CO2 sink using chlorophyll a.
Birthe Zäncker, Michael Cunliffe, and Anja Engel
Biogeosciences, 18, 2107–2118, https://doi.org/10.5194/bg-18-2107-2021, https://doi.org/10.5194/bg-18-2107-2021, 2021
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Fungi are found in numerous marine environments. Our study found an increased importance of fungi in the Ionian Sea, where bacterial and phytoplankton counts were reduced, but organic matter was still available, suggesting fungi might benefit from the reduced competition from bacteria in low-nutrient, low-chlorophyll (LNLC) regions.
Jon Olafsson, Solveig R. Olafsdottir, Taro Takahashi, Magnus Danielsen, and Thorarinn S. Arnarson
Biogeosciences, 18, 1689–1701, https://doi.org/10.5194/bg-18-1689-2021, https://doi.org/10.5194/bg-18-1689-2021, 2021
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The Atlantic north of 50° N is an intense ocean sink area for atmospheric CO2. Observations in the vicinity of Iceland reveal a previously unrecognized Arctic contribution to the North Atlantic CO2 sink. Sustained CO2 influx to waters flowing from the Arctic Ocean is linked to their excess alkalinity derived from sources in the changing Arctic. The results relate to the following question: will the North Atlantic continue to absorb CO2 in the future as it has in the past?
Wei-Lei Wang, Guisheng Song, François Primeau, Eric S. Saltzman, Thomas G. Bell, and J. Keith Moore
Biogeosciences, 17, 5335–5354, https://doi.org/10.5194/bg-17-5335-2020, https://doi.org/10.5194/bg-17-5335-2020, 2020
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Dimethyl sulfide, a volatile compound produced as a byproduct of marine phytoplankton activity, can be emitted to the atmosphere via gas exchange. In the atmosphere, DMS is oxidized to cloud condensation nuclei, thus contributing to cloud formation. Therefore, oceanic DMS plays an important role in regulating the planet's climate by influencing the radiation budget. In this study, we use an artificial neural network model to update the global DMS climatology and estimate the sea-to-air flux.
Yuri Galletti, Silvia Becagli, Alcide di Sarra, Margherita Gonnelli, Elvira Pulido-Villena, Damiano M. Sferlazzo, Rita Traversi, Stefano Vestri, and Chiara Santinelli
Biogeosciences, 17, 3669–3684, https://doi.org/10.5194/bg-17-3669-2020, https://doi.org/10.5194/bg-17-3669-2020, 2020
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This paper reports the first data about atmospheric deposition of dissolved organic matter (DOM) on the island of Lampedusa. It also shows the implications for the surface marine layer by studying the impact of atmospheric organic carbon deposition in the marine ecosystem. It is a preliminary study, but it is pioneering and important for having new data that can be crucial in order to understand the impact of atmospheric deposition on the marine carbon cycle in a global climate change scenario.
Charel Wohl, Ian Brown, Vassilis Kitidis, Anna E. Jones, William T. Sturges, Philip D. Nightingale, and Mingxi Yang
Biogeosciences, 17, 2593–2619, https://doi.org/10.5194/bg-17-2593-2020, https://doi.org/10.5194/bg-17-2593-2020, 2020
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The oceans represent a poorly understood source of organic carbon to the atmosphere. In this paper, we present ship-based measurements of specific compounds in ambient air and seawater of the Southern Ocean. We present fluxes of these gases between air and sea at very high resolution. The data also contain evidence for day and night variations in some of these compounds. These measurements can be used to better understand the role of the Southern Ocean in the cycling of these compounds.
Rebecca L. Jackson, Albert J. Gabric, Roger Cropp, and Matthew T. Woodhouse
Biogeosciences, 17, 2181–2204, https://doi.org/10.5194/bg-17-2181-2020, https://doi.org/10.5194/bg-17-2181-2020, 2020
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Coral reefs are a strong source of atmospheric sulfur through stress-induced emissions of dimethylsulfide (DMS). This biogenic sulfur can influence aerosol and cloud properties and, consequently, the radiative balance over the ocean. DMS emissions may therefore help to mitigate coral physiological stress via increased low-level cloud cover and reduced sea surface temperature. The importance of DMS in coral physiology and climate is reviewed and the implications for coral bleaching are discussed.
Louise Delaigue, Helmuth Thomas, and Alfonso Mucci
Biogeosciences, 17, 547–566, https://doi.org/10.5194/bg-17-547-2020, https://doi.org/10.5194/bg-17-547-2020, 2020
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This paper reports on the first compilation and analysis of the surface water pCO2 distribution in the Saguenay Fjord, the southernmost subarctic fjord in the Northern Hemisphere, and thus fills a significant knowledge gap in current regional estimates of estuarine CO2 emissions.
Tim Fischer, Annette Kock, Damian L. Arévalo-Martínez, Marcus Dengler, Peter Brandt, and Hermann W. Bange
Biogeosciences, 16, 2307–2328, https://doi.org/10.5194/bg-16-2307-2019, https://doi.org/10.5194/bg-16-2307-2019, 2019
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We investigated air–sea gas exchange in oceanic upwelling regions for the case of nitrous oxide off Peru. In this region, routine concentration measurements from ships at 5 m or 10 m depth prove to overestimate surface (bulk) concentration. Thus, standard estimates of gas exchange will show systematic error. This is due to very shallow stratified layers that inhibit exchange between surface water and waters below and can exist for several days. Maximum bias occurs in moderate wind conditions.
Mingxi Yang, Thomas G. Bell, Ian J. Brown, James R. Fishwick, Vassilis Kitidis, Philip D. Nightingale, Andrew P. Rees, and Timothy J. Smyth
Biogeosciences, 16, 961–978, https://doi.org/10.5194/bg-16-961-2019, https://doi.org/10.5194/bg-16-961-2019, 2019
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We quantify the emissions and uptake of the greenhouse gases carbon dioxide and methane from the coastal seas of the UK over 1 year using the state-of-the-art eddy covariance technique. Our measurements show how these air–sea fluxes vary twice a day (tidal), diurnally (circadian) and seasonally. We also estimate the air–sea gas transfer velocity, which is essential for modelling and predicting coastal air-sea exchange.
Riley X. Brady, Nicole S. Lovenduski, Michael A. Alexander, Michael Jacox, and Nicolas Gruber
Biogeosciences, 16, 329–346, https://doi.org/10.5194/bg-16-329-2019, https://doi.org/10.5194/bg-16-329-2019, 2019
Stelios Myriokefalitakis, Akinori Ito, Maria Kanakidou, Athanasios Nenes, Maarten C. Krol, Natalie M. Mahowald, Rachel A. Scanza, Douglas S. Hamilton, Matthew S. Johnson, Nicholas Meskhidze, Jasper F. Kok, Cecile Guieu, Alex R. Baker, Timothy D. Jickells, Manmohan M. Sarin, Srinivas Bikkina, Rachel Shelley, Andrew Bowie, Morgane M. G. Perron, and Robert A. Duce
Biogeosciences, 15, 6659–6684, https://doi.org/10.5194/bg-15-6659-2018, https://doi.org/10.5194/bg-15-6659-2018, 2018
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The first atmospheric iron (Fe) deposition model intercomparison is presented in this study, as a result of the deliberations of the United Nations Joint Group of Experts on the Scientific Aspects of Marine Environmental Protection (GESAMP; http://www.gesamp.org/) Working Group 38. We conclude that model diversity over remote oceans reflects uncertainty in the Fe content parameterizations of dust aerosols, combustion aerosol emissions and the size distribution of transported aerosol Fe.
Liliane Merlivat, Jacqueline Boutin, David Antoine, Laurence Beaumont, Melek Golbol, and Vincenzo Vellucci
Biogeosciences, 15, 5653–5662, https://doi.org/10.5194/bg-15-5653-2018, https://doi.org/10.5194/bg-15-5653-2018, 2018
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The fugacity of carbon dioxide in seawater (fCO2) was measured hourly in the surface waters of the NW Mediterranean Sea during two 3-year sequences separated by 18 years. A decrease of pH of 0.0022 yr−1 was computed. About 85 % of the accumulation of dissolved inorganic carbon (DIC) comes from chemical equilibration with increasing atmospheric CO2; the remaining 15 % accumulation is consistent with estimates of transfer of Atlantic waters through the Gibraltar Strait.
Amanda R. Fay, Nicole S. Lovenduski, Galen A. McKinley, David R. Munro, Colm Sweeney, Alison R. Gray, Peter Landschützer, Britton B. Stephens, Taro Takahashi, and Nancy Williams
Biogeosciences, 15, 3841–3855, https://doi.org/10.5194/bg-15-3841-2018, https://doi.org/10.5194/bg-15-3841-2018, 2018
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The Southern Ocean is highly under-sampled and since this region dominates the ocean sink for CO2, understanding change is critical. Here we utilize available observations to evaluate how the seasonal cycle, variability, and trends in surface ocean carbon in the well-sampled Drake Passage region compare to that of the broader subpolar Southern Ocean. Results indicate that the Drake Passage is representative of the broader region; however, additional winter observations would improve comparisons.
Cui-Ci Sun, Martin Sperling, and Anja Engel
Biogeosciences, 15, 3577–3589, https://doi.org/10.5194/bg-15-3577-2018, https://doi.org/10.5194/bg-15-3577-2018, 2018
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Biogenic gel particles such as transparent exopolymer particles (TEP) and Coomassie stainable particles (CSP) are important components in the sea-surface microlayer (SML). Their potential role in air–sea gas exchange and in primary organic aerosol emission has generated considerable research interest. Our wind wave channel experiment revealed how wind speed controls the accumulation and size distribution of biogenic gel particles in the SML.
N. Precious Mongwe, Marcello Vichi, and Pedro M. S. Monteiro
Biogeosciences, 15, 2851–2872, https://doi.org/10.5194/bg-15-2851-2018, https://doi.org/10.5194/bg-15-2851-2018, 2018
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Here we analyze seasonal cycle of CO2 biases in 10 CMIP5 models in the SO. We find two main model biases; exaggeration of primary production such that biologically driven DIC changes mainly regulates FCO2 variability, and an overestimation of the role of solubility, such that changes in temperature dominantly drive FCO2 seasonal changes to an extent of opposing biological CO2 uptake in spring. CMIP5 models show greater zonal homogeneity in the seasonal cycle of FCO2 than observational products.
Allison R. Moreno, George I. Hagstrom, Francois W. Primeau, Simon A. Levin, and Adam C. Martiny
Biogeosciences, 15, 2761–2779, https://doi.org/10.5194/bg-15-2761-2018, https://doi.org/10.5194/bg-15-2761-2018, 2018
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To bridge the missing links between variable marine elemental stoichiometry, phytoplankton physiology and carbon cycling, we embed four environmentally controlled stoichiometric models into a five-box ocean model. As predicted each model varied in its influence on the biological pump. Surprisingly, we found that variation can lead to nonlinear controls on atmospheric CO2 and carbon export, suggesting the need for further studies of ocean C : P and the impact on ocean carbon cycling.
Luke Gregor, Schalk Kok, and Pedro M. S. Monteiro
Biogeosciences, 15, 2361–2378, https://doi.org/10.5194/bg-15-2361-2018, https://doi.org/10.5194/bg-15-2361-2018, 2018
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The Southern Ocean accounts for a large portion of the variability in oceanic CO2 uptake. However, the drivers of these changes are not understood due to a lack of observations. In this study, we used an ensemble of gap-filling methods to estimate surface CO2. We found that winter was a more important driver of longer-term variability driven by changes in wind stress. Summer variability of CO2 was driven primarily by increases in primary production.
Erik T. Buitenhuis, Parvadha Suntharalingam, and Corinne Le Quéré
Biogeosciences, 15, 2161–2175, https://doi.org/10.5194/bg-15-2161-2018, https://doi.org/10.5194/bg-15-2161-2018, 2018
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Thanks to decreases in CFC concentrations, N2O is now the third-most important greenhouse gas, and the dominant contributor to stratospheric ozone depletion. Here we estimate the ocean–atmosphere N2O flux. We find that an estimate based on observations alone has a large uncertainty. By combining observations and a range of model simulations we find that the uncertainty is much reduced to 2.45 ± 0.8 Tg N yr−1, and better constrained and at the lower end of the estimate in the latest IPCC report.
Sayaka Yasunaka, Eko Siswanto, Are Olsen, Mario Hoppema, Eiji Watanabe, Agneta Fransson, Melissa Chierici, Akihiko Murata, Siv K. Lauvset, Rik Wanninkhof, Taro Takahashi, Naohiro Kosugi, Abdirahman M. Omar, Steven van Heuven, and Jeremy T. Mathis
Biogeosciences, 15, 1643–1661, https://doi.org/10.5194/bg-15-1643-2018, https://doi.org/10.5194/bg-15-1643-2018, 2018
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We estimated monthly air–sea CO2 fluxes in the Arctic Ocean and its adjacent seas north of 60° N from 1997 to 2014, after mapping pCO2 in the surface water using a self-organizing map technique. The addition of Chl a as a parameter enabled us to improve the estimate of pCO2 via better representation of its decline in spring. The uncertainty in the CO2 flux estimate was reduced, and a net annual Arctic Ocean CO2 uptake of 180 ± 130 Tg C y−1 was determined to be significant.
Alizée Roobaert, Goulven G. Laruelle, Peter Landschützer, and Pierre Regnier
Biogeosciences, 15, 1701–1720, https://doi.org/10.5194/bg-15-1701-2018, https://doi.org/10.5194/bg-15-1701-2018, 2018
Chao Zhang, Huiwang Gao, Xiaohong Yao, Zongbo Shi, Jinhui Shi, Yang Yu, Ling Meng, and Xinyu Guo
Biogeosciences, 15, 749–765, https://doi.org/10.5194/bg-15-749-2018, https://doi.org/10.5194/bg-15-749-2018, 2018
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This study compares the response of phytoplankton growth in the northwest Pacific to those in the Yellow Sea. In general, larger positive responses of phytoplankton induced by combined nutrients (in the subtropical gyre of the northwest Pacific) than those induced by a single nutrient (in the Kuroshio Extension and the Yellow Sea) from the dust are observed. We also emphasize the importance of an increase in bioavailable P stock for phytoplankton growth following dust addition.
Goulven G. Laruelle, Peter Landschützer, Nicolas Gruber, Jean-Louis Tison, Bruno Delille, and Pierre Regnier
Biogeosciences, 14, 4545–4561, https://doi.org/10.5194/bg-14-4545-2017, https://doi.org/10.5194/bg-14-4545-2017, 2017
Melchor González-Dávila, J. Magdalena Santana Casiano, and Francisco Machín
Biogeosciences, 14, 3859–3871, https://doi.org/10.5194/bg-14-3859-2017, https://doi.org/10.5194/bg-14-3859-2017, 2017
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The Mauritanian–Cap Vert upwelling is shown to be sensitive to climate change forcing on upwelling processes, which strongly affects the CO2 surface distribution, ocean acidification rates, and air–sea CO2 exchange. We confirmed an upwelling intensification, an increase in the CO2 outgassing, and an important decrease in the pH of the surface waters. Upwelling areas are poorly studied and VOS lines are shown as one of the most significant contributors to our knowledge of the ocean's response.
Rachel Hussherr, Maurice Levasseur, Martine Lizotte, Jean-Éric Tremblay, Jacoba Mol, Helmuth Thomas, Michel Gosselin, Michel Starr, Lisa A. Miller, Tereza Jarniková, Nina Schuback, and Alfonso Mucci
Biogeosciences, 14, 2407–2427, https://doi.org/10.5194/bg-14-2407-2017, https://doi.org/10.5194/bg-14-2407-2017, 2017
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This study assesses the impact of ocean acidification on phytoplankton and its synthesis of the climate-active gas dimethyl sulfide (DMS), as well as its modulation, by two contrasting light regimes in the Arctic. The light regimes tested had no significant impact on either the phytoplankton or DMS concentration, whereas both variables decreased linearly with the decrease in pH. Thus, a rapid decrease in surface water pH could alter the algal biomass and inhibit DMS production in the Arctic.
Cited articles
Andreae, M. O.: Ocean-atmosphere interactions in the global biogeochemical
sulfur cycle, Mar. Chem., 30, 1–29,
https://doi.org/10.1016/0304-4203(90)90059-L, 1990.
Andreae, M. O. and Crutzen, P. J.: Atmospheric aerosols: Biogeochemical
sources and role in atmospheric chemistry, Science, 276, 1052–1058,
https://doi.org/10.1126/science.276.5315.1052, 1997.
Archer, S. D., Widdicombe, C. E., Tarran, G. A., Rees, A. P., and Burkill,
P. H.: Production and turnover of particulate dimethylsulphoniopropionate
during a coccolithophore bloom in the northern North Sea, Aquat. Microb.
Ecol., 24, 225–241, https://doi.org/10.3354/ame024225, 2001.
Arneth, A., Monson, R. K., Schurgers, G., Niinemets, Ü., and Palmer, P. I.: Why are estimates of global terrestrial isoprene emissions so similar (and why is this not so for monoterpenes)?, Atmos. Chem. Phys., 8, 4605–4620, https://doi.org/10.5194/acp-8-4605-2008, 2008.
Arnold, S. R., Spracklen, D. V., Williams, J., Yassaa, N., Sciare, J., Bonsang, B., Gros, V., Peeken, I., Lewis, A. C., Alvain, S., and Moulin, C.: Evaluation of the global oceanic isoprene source and its impacts on marine organic carbon aerosol, Atmos. Chem. Phys., 9, 1253–1262, https://doi.org/10.5194/acp-9-1253-2009, 2009.
Baker, A. R., Turner, S. M., Broadgate, W. J., Thompson, A., McFiggans, G.
B., Vesperini, O., Nightingale, P. D., Liss, P. S., and Jickells, T. D.:
Distribution and sea-air fluxes of biogenic trace gases in the eastern
Atlantic Ocean, Global Biogeochem. Cy., 14, 871–886,
https://doi.org/10.1029/1999gb001219, 2000.
Bonsang, B., Polle, C., and Lambert, G.: Evidence for marine production of
isoprene, Geophys. Res. Lett., 19, 1129–1132,
https://doi.org/10.1029/92gl00083, 1992.
Booge, D., Marandino, C. A., Schlundt, C., Palmer, P. I., Schlundt, M., Atlas, E. L., Bracher, A., Saltzman, E. S., and Wallace, D. W. R.: Can simple models predict large-scale surface ocean isoprene concentrations?, Atmos. Chem. Phys., 16, 11807–11821, https://doi.org/10.5194/acp-16-11807-2016, 2016.
Booge, D., Schlundt, C., Bracher, A., Endres, S., Zäncker, B., and Marandino, C. A.: Marine isoprene production and consumption in the mixed layer of the surface ocean – a field study over two oceanic regions, Biogeosciences, 15, 649–667, https://doi.org/10.5194/bg-15-649-2018, 2018.
Bouillon, R.-C., Lee, P. A., de Mora, S. J., Levasseur, M., and Lovejoy, C.:
Vernal distribution of dimethylsulphide, dimethylsulphoniopropionate, and
dimethylsulphoxide in the North Water in 1998, Deep-Sea Res. Pt. II, 49, 5171–5189,
https://doi.org/10.1016/S0967-0645(02)00184-4, 2002.
Broadbent, A. D., Jones, G. B., and Jones, R. J.: DMSP in corals and benthic
algae from the Great Barrier Reef, Estuar. Coast. Shelf S., 55,
547–555, https://doi.org/10.1006/ecss.2002.1021, 2002.
Broadgate, W. J., Liss, P. S., and Penkett, S. A.: Seasonal emissions of
isoprene and other reactive hydrocarbon gases from the ocean, Geophys.
Res. Lett., 24, 2675–2678, https://doi.org/10.1029/97gl02736, 1997.
Broadgate, W. J., Malin, G., Kupper, F. C., Thompson, A., and Liss, P. S.:
Isoprene and other non-methane hydrocarbons from seaweeds: a source of
reactive hydrocarbons to the atmosphere, Mar. Chem., 88, 61–73,
https://doi.org/10.1016/j.marchem.2004.03.002, 2004.
Cantoni, G. L. and Anderson, D. G.: Enzymatic cleavage of
dimethylpropiothetin by polysiphonia lanosa, J. Biol.
Chem., 222, 171–177, https://doi.org/10.1016/S0021-9258(19)50782-7,
1956.
Carpenter, L. J., Archer, S. D., and Beale, R.: Ocean-atmosphere trace gas
exchange, Chem. Soc. Rev., 41, 6473–6506,
https://doi.org/10.1039/C2CS35121H, 2012.
Cerqueira, M. and Pio, C.: Production and release of dimethylsulphide from
an estuary in Portugal, Atmos. Environ., 33, 3355–3366,
https://doi.org/10.1016/S1352-2310(98)00378-1, 1999.
Charlson, R. J., Lovelock, J. E., Andreae, M. O., and Warren, S. G.: Oceanic
phytoplankton, atmospheric sulfur, cloud albedo and climate, Nature, 326,
655–661, https://doi.org/10.1038/326655a0, 1987.
Chen, Q., Sherwen, T., Evans, M., and Alexander, B.: DMS oxidation and sulfur aerosol formation in the marine troposphere: a focus on reactive halogen and multiphase chemistry, Atmos. Chem. Phys., 18, 13617–13637, https://doi.org/10.5194/acp-18-13617-2018, 2018.
Claeys, M., Graham, B., Vas, G., Wang, W., Vermeylen, R., Pashynska, V.,
Cafmeyer, J., Guyon, P., Andreae, M. O., Artaxo, P., and Maenhaut, W.:
Formation of secondary organic aerosols through photooxidation of isoprene,
Science, 303, 1173–1176, https://doi.org/10.1126/science.1092805, 2004.
Curran, M. A. and Jones, G. B.: Dimethyl sulfide in the Southern Ocean:
Seasonality and flux, J. Geophys. Res.-Atmos., 105,
20451–20459, https://doi.org/10.1029/2000JD900176, 2000.
Curran, M. A. J., Jones, G. B., and Burton, H.: Spatial distribution of
dimethylsulfide and dimethylsulfoniopropionate in the Australasian sector of
the Southern Ocean, J. Geophys. Res.-Atmos., 103,
16677–16689, https://doi.org/10.1029/97jd03453, 1998.
Curson, A. R. J., Todd, J. D., Sullivan, M. J., and Johnston, A. W. B.:
Catabolism of dimethylsulphoniopropionate: microorganisms, enzymes and
genes, Nat. Rev. Microbiol., 9, 849–859,
https://doi.org/10.1038/nrmicro2653, 2011.
Emerson, S., Stump, C., Wilbur, D., and Quay, P.: Accurate measurement of
O2, N2, and Ar gases in water and the solubility of N2, Mar. Chem.,
64, 337–347, https://doi.org/10.1016/s0304-4203(98)00090-5, 1999.
Exton, D. A., Suggett, D. J., McGenity, T. J., and Steinke, M.:
Chlorophyll-normalized isoprene production in laboratory cultures of marine
microalgae and implications for global models, Limnol. Oceanogr.,
58, 1301–1311, https://doi.org/10.4319/lo.2013.58.4.1301, 2013.
Fiddes, S. L., Woodhouse, M. T., Nicholls, Z., Lane, T. P., and Schofield, R.: Cloud, precipitation and radiation responses to large perturbations in global dimethyl sulfide, Atmos. Chem. Phys., 18, 10177–10198, https://doi.org/10.5194/acp-18-10177-2018, 2018.
Gibson, J. A., Garrick, R. C., Burton, H. R., and McTaggart, A. R.:
Dimethysulfide concentrations in the ocean close to the antarctic continent,
Geomicrobiol. J., 6, 179–184,
https://doi.org/10.1080/01490458809377837, 1988.
Guenther, A., Hewitt, C. N., Erickson, D., Fall, R., Geron, C., Graedel, T.,
Harley, P., Klinger, L., Lerdau, M., McKay, W. A., Pierce, T., Scholes, B.,
Steinbrecher, R., Tallamraju, R., Taylor, J., and Zimmerman, P.: A global model of natural volatile organic compound emissions, J.
Geophys. Res.-Atmos., 100, 8873–8892,
https://doi.org/10.1029/94jd02950, 1995.
Guenther, A., Karl, T., Harley, P., Wiedinmyer, C., Palmer, P. I., and Geron, C.: Estimates of global terrestrial isoprene emissions using MEGAN (Model of Emissions of Gases and Aerosols from Nature), Atmos. Chem. Phys., 6, 3181–3210, https://doi.org/10.5194/acp-6-3181-2006, 2006.
Guenther, A. B., Jiang, X., Heald, C. L., Sakulyanontvittaya, T., Duhl, T., Emmons, L. K., and Wang, X.: The Model of Emissions of Gases and Aerosols from Nature version 2.1 (MEGAN2.1): an extended and updated framework for modeling biogenic emissions, Geosci. Model Dev., 5, 1471–1492, https://doi.org/10.5194/gmd-5-1471-2012, 2012.
Hackenberg, S., Andrews, S. J., Airs, R., Arnold, S., Bouman, H., Brewin,
R., Chance, R. J., Cummings, D., Dall'Olmo, G., and Lewis, A.: Potential
controls of isoprene in the surface ocean, Global Biogeochem. Cy., 31,
644–662, https://doi.org/10.1002/2016GB005531, 2017.
Hatton, A. D., Darroch, L., and Malin, G.: The role of dimethylsulphoxide in
the marine biogeochemical cycle of dimethylsulphide, Oceanogr. Mar. Biol. Ann.
Rev., 42, 29–55, 2004.
Hatton, A. D., Shenoy, D. M., Hart, M. C., Mogg, A., and Green, D. H.:
Metabolism of DMSP, DMS and DMSO by the cultivable bacterial community
associated with the DMSP-producing dinoflagellate Scrippsiella trochoidea,
Biogeochemistry, 110, 131–146, https://doi.org/10.1007/s10533-012-9702-7,
2012.
Hauck, J., Völker, C., Wang, T., Hoppema, M., Losch, M., and
Wolf-Gladrow, D. A.: Seasonally different carbon flux changes in the
Southern Ocean in response to the southern annular mode, Global
Biogeochem. Cy., 27, 1236–1245, https://doi.org/10.1002/2013gb004600,
2013.
Houghton, J. T., Ding, Y., Griggs, D. J., Noguer, M., van der Linden, P. J., Dai, X., Maskell, K., and Johnson, C.: Climate Change 2001: The Scientific Basis. Contribution of Working Group I to the Third Assessment Report of the Intergovernmental Panel on Climate Change, The Press Syndicate of the University of Cambridge, United Kingdom and New York, NY, USA, 881 pp., 2001.
Hsu, S., Meindl, E. A., and Gilhousen, D. B.: Determining the power-law
wind-profile exponent under near-neutral stability conditions at sea,
J. Appl. Meteorol. Clim., 33, 757–765,
https://doi.org/10.1175/1520-0450(1994)033<0757:DTPLWP>2.0.CO;2, 1994.
Hulswar, S., Simó, R., Galí, M., Bell, T. G., Lana, A., Inamdar, S., Halloran, P. R., Manville, G., and Mahajan, A. S.: Third revision of the global surface seawater dimethyl sulfide climatology (DMS-Rev3), Earth Syst. Sci. Data, 14, 2963–2987, https://doi.org/10.5194/essd-14-2963-2022, 2022.
Inomata, Y., Hayashi, M., Osada, K., and Iwasaka, Y.: Spatial distributions
of volatile sulfur compounds in surface seawater and overlying atmosphere in
the northwestern Pacific Ocean, eastern Indian Ocean, and Southern Ocean,
Global Biogeochem. Cy., 20, GB2022, https://doi.org/10.1029/2005GB002518,
2006.
Jackson, R. L., Gabric, A. J., Cropp, R., and Woodhouse, M. T.: Dimethylsulfide (DMS), marine biogenic aerosols and the ecophysiology of coral reefs, Biogeosciences, 17, 2181–2204, https://doi.org/10.5194/bg-17-2181-2020, 2020.
Jiang, H.: Evaluation of altimeter undersampling in estimating global wind
and wave climate using virtual observation, Remote Sens. Environ.,
245, 111840, https://doi.org/10.1016/j.rse.2020.111840, 2020.
Jones, G. B., Curran, M. A., Swan, H. B., Greene, R. M., Griffiths, F. B.,
and Clementson, L. A.: Influence of different water masses and biological
activity on dimethylsulphide and dimethylsulphoniopropionate in the
subantarctic zone of the Southern Ocean during ACE 1, J. Geophys.
Res.-Atmos., 103, 16691–16701, https://doi.org/10.1029/98JD01200,
1998.
Kameyama, S., Yoshida, S., Tanimoto, H., Inomata, S., Suzuki, K., and
Yoshikawa-Inoue, H.: High-resolution observations of dissolved isoprene in
surface seawater in the Southern Ocean during austral summer 2010–2011,
J. Oceanogr., 70, 225–239,
https://doi.org/10.1007/s10872-014-0226-8, 2014.
Keller, M. D., Bellows, W. K., and Guillard, R. R. L.: Dimethyl sulfide
production in marine-phytoplankton, Acs Sym. Ser., 393, 167–182,
https://doi.org/10.1021/bk-1989-0393.ch011, 1989.
Kettle, A. J., Andreae, M. O., Amouroux, D., Andreae, T. W., Bates, T. S.,
Berresheim, H., Bingemer, H., Boniforti, R., Curran, M. A. J., DiTullio, G.
R., Helas, G., Jones, G. B., Keller, M. D., Kiene, R. P., Leck, C.,
Levasseur, M., Malin, G., Maspero, M., Matrai, P., McTaggart, A. R.,
Mihalopoulos, N., Nguyen, B. C., Novo, A., Putaud, J. P., Rapsomanikis, S.,
Roberts, G., Schebeske, G., Sharma, S., Simo, R., Staubes, R., Turner, S.,
and Uher, G.: A global database of sea surface dimethylsulfide (DMS)
measurements and a procedure to predict sea surface DMS as a function of
latitude, longitude, and month, Global Biogeochem. Cy., 13, 399–444,
https://doi.org/10.1029/1999gb900004, 1999.
Kiene, R. P., Kieber, D. J., Slezak, D., Toole, D. A., del Valle, D. A.,
Bisgrove, J., Brinkley, J., and Rellinger, A.: Distribution and cycling of
dimethylsulfide, dimethylsulfoniopropionate, and dimethylsulfoxide during
spring and early summer in the Southern Ocean south of New Zealand, Aquat.
Sci., 69, 305–319, https://doi.org/10.1007/s00027-007-0892-3, 2007.
Kloster, S., Feichter, J., Maier-Reimer, E., Six, K. D., Stier, P., and Wetzel, P.: DMS cycle in the marine ocean-atmosphere system – a global model study, Biogeosciences, 3, 29–51, https://doi.org/10.5194/bg-3-29-2006, 2006.
Koga, S., Nomura, D., and Wada, M.: Variation of dimethylsulfide mixing
ratio over the Southern Ocean from 36∘ S to 70∘ S, Polar
Sci., 8, 306–313, https://doi.org/10.1016/j.polar.2014.04.002, 2014.
Korhonen, H., Carslaw, K. S., Spracklen, D. V., Mann, G. W., and Woodhouse,
M. T.: Influence of oceanic dimethyl sulfide emissions on cloud condensation
nuclei concentrations and seasonality over the remote Southern Hemisphere
oceans: A global model study, J. Geophys. Res.-Atmos.,
113, D15204, https://doi.org/10.1029/2007jd009718, 2008.
Kulmala, M., Pirjola, U., and Makela, J. M.: Stable sulphate clusters as a
source of new atmospheric particles, Nature, 404, 66–69,
https://doi.org/10.1038/35003550, 2000.
Lana, A., Bell, T. G., Simo, R., Vallina, S. M., Ballabrera-Poy, J., Kettle,
A. J., Dachs, J., Bopp, L., Saltzman, E. S., Stefels, J., Johnson, J. E.,
and Liss, P. S.: An updated climatology of surface dimethlysulfide
concentrations and emission fluxes in the global ocean, Global
Biogeochem. Cy., 25, GB1004, https://doi.org/10.1029/2010gb003850, 2011.
Laothawornkitkul, J., Taylor, J. E., Paul, N. D., and Hewitt, C. N.:
Biogenic volatile organic compounds in the Earth system, New Phytol.,
183, 27–51, https://doi.org/10.1111/j.1469-8137.2009.02859.x, 2009.
Lee, P. and De Mora, S.: DMSP, DMS and DMSO concentrations and temporal trends in marine surface waters at Leigh, New Zealand, in: Biological and environmental chemistry of DMSP and related sulfonium compounds, Springer, Boston, MA, https://doi.org/10.1007/978-1-4613-0377-0_34, 1996.
Lennartz, S. T., Marandino, C. A., von Hobe, M., Cortes, P., Quack, B., Simo, R., Booge, D., Pozzer, A., Steinhoff, T., Arevalo-Martinez, D. L., Kloss, C., Bracher, A., Röttgers, R., Atlas, E., and Krüger, K.: Direct oceanic emissions unlikely to account for the missing source of atmospheric carbonyl sulfide, Atmos. Chem. Phys., 17, 385–402, https://doi.org/10.5194/acp-17-385-2017, 2017.
Li, J. L., Zhai, X., Ma, Z., Zhang, H. H., and Yang, G. P.: Spatial
distributions and sea-to-air fluxes of non-methane hydrocarbons in the
atmosphere and seawater of the Western Pacific Ocean, Sci. Total
Environ., 672, 491–501, https://doi.org/10.1016/j.scitotenv.2019.04.019,
2019.
Li, J. L., Zhai, X., Zhang, H. H., and Yang, G. P.: Temporal variations in
the distribution and sea-to-air flux of marine isoprene in the East China
Sea, Atmos. Environ., 187, 131–143,
https://doi.org/10.1016/j.atmosenv.2018.05.054, 2018.
Liss, P. S.: Trace gas emissions from the marine biosphere, Philos.
T. R. Soc. A, 365, 1697–1704, https://doi.org/10.1098/rsta.2007.2039, 2007.
Liss, P. S. and Slater, P. G.: Flux of gases across air-sea interface,
Nature, 247, 181–184, https://doi.org/10.1038/247181a0, 1974.
Liss, P. S., Marandino, C. A., and Dahl, E. E.: Short-lived trace gases in the surface ocean and the atmosphere, in: Ocean-Atmosphere Interactions of Gases and Particles, Springer, Berlin, Heidelberg, 1–54, https://doi.org/10.1007/978-3-642-25643-1_1, 2014.
Lovelock, J. E., Maggs, R. J., and Rasmusse.Ra: Atmospheric dimethyl sulfide
and natural sulfur cycle, Nature, 237, 452–453,
https://doi.org/10.1038/237452a0, 1972.
Luis, A. J. and Lotlikar, V. R.: Hydrographic characteristics along two XCTD
sections between Africa and Antarctica during austral summer 2018, Polar
Sci., 30, 100705, https://doi.org/10.1016/j.polar.2021.100705, 2021.
Mahajan, A. S., Fadnavis, S., Thomas, M. A., Pozzoli, L., Gupta, S., Royer,
S. J., Saiz-Lopez, A., and Simo, R.: Quantifying the impacts of an updated
global dimethyl sulfide climatology on cloud microphysics and aerosol
radiative forcing, J. Geophys. Res.-Atmos., 120,
2524–2536, https://doi.org/10.1002/2014jd022687, 2015.
Mahmood, R., von Salzen, K., Norman, A.-L., Galí, M., and Levasseur, M.: Sensitivity of Arctic sulfate aerosol and clouds to changes in future surface seawater dimethylsulfide concentrations, Atmos. Chem. Phys., 19, 6419–6435, https://doi.org/10.5194/acp-19-6419-2019, 2019.
Matsunaga, S., Mochida, M., Saito, T., and Kawamura, K.: In situ measurement
of isoprene in the marine air and surface seawater from the western North
Pacific, Atmos. Environ., 36, 6051–6057,
https://doi.org/10.1016/s1352-2310(02)00657-x, 2002.
McArdle, N., Liss, P., and Dennis, P.: An isotopic study of atmospheric
sulphur at three sites in Wales and at Mace Head, Eire, J.
Geophys. Res.-Atmos., 103, 31079–31094,
https://doi.org/10.1029/98jd01664, 1998.
McGillis, W. R., Dacey, J. W. H., Frew, N. M., Bock, E. J., and Nelson, R.
K.: Water-air flux of dimethylsulfide, J. Geophys. Res.-Oceans, 105, 1187–1193, https://doi.org/10.1029/1999jc900243, 2000.
McTaggart, A. R. and Burton, H.: Dimethyl Sulfide concentrations in the
surface waters of the Australasian Antarctic and Subantarctic Oceans during
an austral summer, J. Geophys. Res.-Oceans, 97, 14407–14412,
https://doi.org/10.1029/92JC01025, 1992.
Milne, P. J., Riemer, D. D., Zika, R. G., and Brand, L. E.: Measurement of
vertical-distribution of isoprene in surface seawater, its chemical fate,
and its emission from several phytoplankton monocultures, Mar. Chem.,
48, 237–244, https://doi.org/10.1016/0304-4203(94)00059-m, 1995.
Monson, R. K. and Holland, E. A.: Biospheric trace gas fluxes and their
control over tropospheric chemistry, Annu. Rev. Ecol.
Syst., 32, 547–576,
https://doi.org/10.1146/annurev.ecolsys.32.081501.114136, 2001.
Moore, R. and Wang, L.: The influence of iron fertilization on the fluxes of
methyl halides and isoprene from ocean to atmosphere in the SERIES
experiment, Deep-Sea Res. Pt. II, 53,
2398–2409, https://doi.org/10.1016/j.dsr2.2006.05.025, 2006.
Mopper, K. and Kieber, D. J.: Photochemistry and the Cycling of
Carbon, Sulfur, Nitrogen and Phosphorus, in: Biogeochemistry of Marine
Dissolved Organic Matter, edited by: Hansell, D. A. and Carlson, C. A., chap. 9, Academic
Press, San Diego, https://doi.org/10.1016/C2012-0-02714-7, 2002.
Naval Oceanographic Office: K10 Global 10 km Analyzed SST data set,
Ver. 1.0, PO.DAAC, CA, USA, Naval Oceanographic Office [data set],
https://doi.org/10.5067/GHK10-41N01 2008.
Nguyen, B., Mihalopoulos, N., and Belviso, S.: Seasonal variation of
atmospheric dimethylsulfide at Amsterdam Island in the southern Indian
Ocean, J. Atmos. Chem., 11, 123–141,
https://doi.org/10.1007/BF00053671, 1990.
Nguyen, B., Mihalopoulos, N., Putaud, J., Gaudry, A., Gallet, L., Keene, W.,
and Galloway, J.: Covariations in oceanic dimethyl sulfide, its oxidation
products and rain acidity at Amsterdam Island in the southern Indian Ocean,
J. Atmos. Chem., 15, 39–53,
https://doi.org/10.1007/BF0005360, 1992.
Nightingale, P. D., Malin, G., Law, C. S., Watson, A. J., Liss, P. S.,
Liddicoat, M. I., Boutin, J., and Upstill-Goddard, R. C.: In situ evaluation
of air-sea gas exchange parameterizations using novel conservative and
volatile tracers, Global Biogeochem. Cy., 14, 373–387,
https://doi.org/10.1029/1999gb900091, 2000.
Ooki, A., Nomura, D., Nishino, S., Kikuchi, T., and Yokouchi, Y.: A
global-scale map of isoprene and volatile organic iodine in surface seawater
of the Arctic, Northwest Pacific, Indian, and Southern Oceans, J.
Geophys. Res.-Oceans, 120, 4108–4128,
https://doi.org/10.1002/2014jc010519, 2015.
Otte, M. L., Wilson, G., Morris, J. T., and Moran, B. M.:
Dimethylsulphoniopropionate (DMSP) and related compounds in higher plants,
J. Exp. Bot., 55, 1919–1925,
https://doi.org/10.1093/jxb/erh178, 2004.
Palmer, P. I. and Shaw, S. L.: Quantifying global marine isoprene fluxes
using MODIS chlorophyll observations, Geophys. Res. Lett., 32, L09805,
https://doi.org/10.1029/2005gl022592, 2005.
Ryan-Keogh, T.: SCALE Winter SDS (1.0), Zenodo [data set], https://doi.org/10.5281/zenodo.6367853, 2022.
Rodríguez-Ros, P., Cortés, P., Robinson, C. M., Nunes, S., Hassler,
C., Royer, S.-J., Estrada, M., Sala, M. M., and Simó, R.: Distribution
and drivers of marine isoprene concentration across the Southern Ocean,
Atmosphere, 11, 556, https://doi.org/10.3390/atmos11060556, 2020.
Sanchez, K. J., Chen, C. L., Russell, L. M., Betha, R., Liu, J., Price, D.
J., Massoli, P., Ziemba, L. D., Crosbie, E. C., Moore, R. H., Muller, M.,
Schiller, S. A., Wisthaler, A., Lee, A. K. Y., Quinn, P. K., Bates, T. S.,
Porter, J., Bell, T. G., Saltzman, E. S., Vaillancourt, R. D., and
Behrenfeld, M. J.: Substantial Seasonal Contribution of Observed Biogenic
Sulfate Particles to Cloud Condensation Nuclei, Sci. Rep.-UK, 8, 3235,
https://doi.org/10.1038/s41598-018-21590-9, 2018.
Sharkey, T. D., Wiberley, A. E., and Donohue, A. R.: Isoprene emission from
plants: Why and how, Ann. Bot., 101, 5–18,
https://doi.org/10.1093/aob/mcm240, 2008.
Shaw, S. L., Chisholm, S. W., and Prinn, R. G.: Isoprene production by
Prochlorococcus, a marine cyanobacterium, and other phytoplankton, Mar.
Chem., 80, 227–245, https://doi.org/10.1016/s0304-4203(02)00101-9, 2003.
Simó, R. and Vila-Costa, M.: Ubiquity of algal dimethylsulfoxide in the
surface ocean: Geographic and temporal distribution patterns, Mar.
Chem., 100, 136–146, https://doi.org/10.1016/j.marchem.2005.11.006,
2006.
Simó, R., Pedrós-Alió, C., Malin, G., and Grimalt, J. O.: Biological turnover of DMS, DMSP and DMSO in contrasting open-sea waters, Mar. Ecol.-Prog. Ser., 203, 1–11, https://doi.org/10.3354/meps203001, 2000.
Stefels, J., Steinke, M., Turner, S., Malin, G., and Belviso, S.:
Environmental constraints on the production and removal of the climatically
active gas dimethylsulphide (DMS) and implications for ecosystem modelling,
Biogeochemistry, 83, 245–275, https://doi.org/10.1007/s10533-007-9091-5,
2007.
Thomas, M. A., Suntharalingam, P., Pozzoli, L., Rast, S., Devasthale, A., Kloster, S., Feichter, J., and Lenton, T. M.: Quantification of DMS aerosol-cloud-climate interactions using the ECHAM5-HAMMOZ model in a current climate scenario, Atmos. Chem. Phys., 10, 7425–7438, https://doi.org/10.5194/acp-10-7425-2010, 2010.
Tortell, P. D. and Long, M. C.: Spatial and temporal variability of biogenic
gases during the Southern Ocean spring bloom, Geophys. Res. Lett.,
36, L01603, https://doi.org/10.1029/2008gl035819, 2009.
Tran, S., Bonsang, B., Gros, V., Peeken, I., Sarda-Esteve, R., Bernhardt, A., and Belviso, S.: A survey of carbon monoxide and non-methane hydrocarbons in the Arctic Ocean during summer 2010, Biogeosciences, 10, 1909–1935, https://doi.org/10.5194/bg-10-1909-2013, 2013.
UK Met Office: OSTIA L4 SST Analysis (GDS2), Ver. 2.0, PO.DAAC, CA,
USA, UK Met Office [data set], https://doi.org/10.5067/GHOST-4FK02, 2012.
Vallina, S. M. and Simó, R.: Strong relationship between DMS and the solar
radiation dose over the global surface ocean, Science, 315, 506–508,
https://doi.org/10.1126/science.1133680, 2007.
Van Alstyne, K. L.: The distribution of DMSP in green macroalgae from
northern New Zealand, eastern Australia and southern Tasmania, J.
Mar. Biol. Assoc. UK, 88, 799–805,
https://doi.org/10.1017/s0025315408001562, 2008.
Vandemark, D., Salisbury, J. E., Hunt, C. W., Shellito, S. M., Irish, J.,
McGillis, W., Sabine, C., and Maenner, S.: Temporal and spatial dynamics of
CO2 air-sea flux in the Gulf of Maine, J. Geophys. Res.-Oceans, 116, C01012, https://doi.org/10.1029/2010JC006408, 2011.
Vogt, M. and Liss, P.: Dimethylsulfide and climate, Surface ocean-lower
atmosphere processes, Anthropocene, 187, 197–232, https://doi.org/10.1016/j.ancene.2015.11.001, 2009.
von Glasow, R. and Crutzen, P. J.: Model study of multiphase DMS oxidation with a focus on halogens, Atmos. Chem. Phys., 4, 589–608, https://doi.org/10.5194/acp-4-589-2004, 2004.
Wanninkhof, R.: Relationship between wind speed and gas exchange over the
ocean, J. Geophys. Res.-Oceans, 97, 7373–7382,
https://doi.org/10.1029/92JC00188, 1992.
Wanninkhof, R.: Relationship between wind speed and gas exchange over the
ocean revisited, Limnol. Oceanogr.-Meth., 12, 351–362,
https://doi.org/10.4319/lom.2014.12.351, 2014.
Went, F. W.: Blue Hazes in the Atmosphere, Nature, 187, 641–643,
https://doi.org/10.1038/187641a0, 1960.
Wiggert, J., Dickey, T., and Granata, T.: The effect of temporal
undersampling on primary production estimates, J. Geophys.
Res.-Oceans, 99, 3361–3371, https://doi.org/10.1029/93JC03163, 1994.
Wohl, C., Brown, I., Kitidis, V., Jones, A. E., Sturges, W. T., Nightingale, P. D., and Yang, M.: Underway seawater and atmospheric measurements of volatile organic compounds in the Southern Ocean, Biogeosciences, 17, 2593–2619, https://doi.org/10.5194/bg-17-2593-2020, 2020.
Yang, J. and Yang, G.-P.: Distribution of dissolved and particulate
dimethylsulfoxide in the East China Sea in winter, Mar. Chem., 127,
199–209, https://doi.org/10.1016/j.marchem.2011.09.006, 2011.
Yang, M., Blomquist, B., Fairall, C., Archer, S., and Huebert, B.: Air-sea
exchange of dimethylsulfide in the Southern Ocean: Measurements from SO
GasEx compared to temperate and tropical regions, J. Geophys. Res.-Oceans, 116, C00F05, https://doi.org/10.1029/2010JC006526, 2011.
Yoch, D. C.: Dimethylsulfoniopropionate: Its sources, role in the marine
food web, and biological degradation to dimethylsulfide, Appl.
Environ. Microbiol., 68, 5804–5815,
https://doi.org/10.1128/aem.68.12.5804-5815.2002, 2002.
Zavarsky, A., Goddijn-Murphy, L., Steinhoff, T., and Marandino, C. A.:
Bubble-Mediated Gas Transfer and Gas Transfer Suppression of DMS and CO2,
J. Geophys. Res.-Atmos., 123, 6624–6647,
https://doi.org/10.1029/2017jd028071, 2018.
Zhang, M., Marandino, C. A., Chen, L., Sun, H., Gao, Z., Park, K., Kim, I.,
Yang, B., Zhu, T., and Yan, J.: Characteristics of the surface water DMS and
pCO2 distributions and their relationships in the Southern Ocean, southeast
Indian Ocean, and northwest Pacific Ocean, Global Biogeochem. Cy., 31,
1318–1331, https://doi.org/10.1002/2017GB005637, 2017.
Zhang, M., Park, K.-T., Yan, J., Park, K., Wu, Y., Jang, E., Gao, W., Tan,
G., Wang, J., and Chen, L.: Atmospheric dimethyl sulfide and its significant
influence on the sea-to-air flux calculation over the Southern Ocean,
Prog. Oceanogr., 186, 102392,
https://doi.org/10.1016/j.pocean.2020.102392, 2020.
Zhang, M. M., Gao, W., Yan, J. P., Wu, Y. F., Marandino, C. A., Park, K.,
Chen, L. Q., Lin, Q., Tan, G. B., and Pan, M. J.: An integrated sampler for
shipboard underway measurement of dimethyl sulfide in surface seawater and
air, Atmos. Environ., 209, 86–91,
https://doi.org/10.1016/j.atmosenv.2019.04.022, 2019.
Zhou, L., Booge, D., Zhang, M., and Marandino, C. A.: Winter time trace gas concentrations during SCALE in 2019, Zenodo [data set], https://doi.org/10.5281/zenodo.7185513, 2022.
Zindler, C., Bracher, A., Marandino, C. A., Taylor, B., Torrecilla, E., Kock, A., and Bange, H. W.: Sulphur compounds, methane, and phytoplankton: interactions along a north–south transit in the western Pacific Ocean, Biogeosciences, 10, 3297–3311, https://doi.org/10.5194/bg-10-3297-2013, 2013.
Zindler, C., Lutterbeck, H., Endres, S., and Bange, H. W.: Environmental
control of dimethylsulfoxide (DMSO) cycling under ocean acidification,
Environ. Chem., 13, 330–339, https://doi.org/10.1071/EN14270, 2015.
Zindler, C., Marandino, C. A., Bange, H. W., Schutte, F., and Saltzman, E.
S.: Nutrient availability determines dimethyl sulfide and isoprene
distribution in the eastern Atlantic Ocean, Geophys. Res. Lett.,
41, 3181–3188, https://doi.org/10.1002/2014gl059547, 2014.
Zubkov, M. V., Fuchs, B. M., Archer, S. D., Kiene, R. P., Amann, R., and
Burkill, P. H.: Rapid turnover of dissolved DMS and DMSP by defined
bacterioplankton communities in the stratified euphotic zone of the North
Sea, Deep-Sea Res. Pt. II, 49,
3017–3038, https://doi.org/10.1016/s0967-0645(02)00069-3, 2002.
Short summary
Trace gas air–sea exchange exerts an important control on air quality and climate, especially in the Southern Ocean (SO). Almost all of the measurements there are skewed to summer, but it is essential to expand our measurement database over greater temporal and spatial scales. Therefore, we report measured concentrations of dimethylsulfide (DMS, as well as related sulfur compounds) and isoprene in the Atlantic sector of the SO. The observations of isoprene are the first in the winter in the SO.
Trace gas air–sea exchange exerts an important control on air quality and climate, especially in...
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