Articles | Volume 20, issue 5
https://doi.org/10.5194/acp-20-3061-2020
© Author(s) 2020. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/acp-20-3061-2020
© Author(s) 2020. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Research article
| Highlight paper
| 
16 Mar 2020
Research article | Highlight paper |
| 16 Mar 2020
| 16 Mar 2020
Methanethiol, dimethyl sulfide and acetone over biologically productive waters in the southwest Pacific Ocean
Sarah J. Lawson
CORRESPONDING AUTHOR
Commonwealth Scientific and Industrial Research Organisation (CSIRO), Oceans and Atmosphere, Aspendale, Australia
Cliff S. Law
National Institute of Water and Atmospheric Research (NIWA), Wellington, New Zealand
Department of Chemistry, University of Otago, Dunedin, New Zealand
Mike J. Harvey
National Institute of Water and Atmospheric Research (NIWA), Wellington, New Zealand
Thomas G. Bell
Plymouth Marine Laboratory, Plymouth, UK
Carolyn F. Walker
National Institute of Water and Atmospheric Research (NIWA), Wellington, New Zealand
Warren J. de Bruyn
Schmid College of Science and Technology, Chapman University,
Orange, California, USA
Eric S. Saltzman
Earth System Science, University of California, Irvine, California,
USA
Related authors
Melita Keywood, Paul Selleck, Fabienne Reisen, David Cohen, Scott Chambers, Min Cheng, Martin Cope, Suzanne Crumeyrolle, Erin Dunne, Kathryn Emmerson, Rosemary Fedele, Ian Galbally, Rob Gillett, Alan Griffiths, Elise-Andree Guerette, James Harnwell, Ruhi Humphries, Sarah Lawson, Branka Miljevic, Suzie Molloy, Jennifer Powell, Jack Simmons, Zoran Ristovski, and Jason Ward
Earth Syst. Sci. Data, 11, 1883–1903, https://doi.org/10.5194/essd-11-1883-2019, https://doi.org/10.5194/essd-11-1883-2019, 2019
Short summary
Short summary
The Sydney Particle Study increased scientific knowledge of the processes leading to particle formation and transformations in Sydney through two comprehensive observation programs which are described in detail here. The data set and its analysis underpin comprehensive chemical transport modelling tools that can be used to assist in the development of a long-term control strategy for particles in Sydney and thus reduce the impact of particles on human health.
Erin Dunne, Ian E. Galbally, Min Cheng, Paul Selleck, Suzie B. Molloy, and Sarah J. Lawson
Atmos. Meas. Tech., 11, 141–159, https://doi.org/10.5194/amt-11-141-2018, https://doi.org/10.5194/amt-11-141-2018, 2018
Short summary
Short summary
A comparison of measurements of 7 volatile organic compounds (VOCs) in urban air by 3 different methods is presented. An uncertainty was calculated for each method and VOCs measured to provide some idea of the reliability of the data. Even when this uncertainty was accounted for, the measurements from the different methods did not agree for 4 of the 7 VOCs. Thus, there is unaccounted uncertainty in VOC measurements which must be considered when utilizing the data and assessing their reliability.
Marc D. Mallet, Maximilien J. Desservettaz, Branka Miljevic, Andelija Milic, Zoran D. Ristovski, Joel Alroe, Luke T. Cravigan, E. Rohan Jayaratne, Clare Paton-Walsh, David W. T. Griffith, Stephen R. Wilson, Graham Kettlewell, Marcel V. van der Schoot, Paul Selleck, Fabienne Reisen, Sarah J. Lawson, Jason Ward, James Harnwell, Min Cheng, Rob W. Gillett, Suzie B. Molloy, Dean Howard, Peter F. Nelson, Anthony L. Morrison, Grant C. Edwards, Alastair G. Williams, Scott D. Chambers, Sylvester Werczynski, Leah R. Williams, V. Holly L. Winton, Brad Atkinson, Xianyu Wang, and Melita D. Keywood
Atmos. Chem. Phys., 17, 13681–13697, https://doi.org/10.5194/acp-17-13681-2017, https://doi.org/10.5194/acp-17-13681-2017, 2017
Short summary
Short summary
Fires play an important role within atmosphere. Gaseous and aerosol emissions influence Earth's temperature but these emissions can vary drastically across region and season. The SAFIRED (Savannah Fires in the Early Dry Season) campaign was undertaken at the Australian Tropical Research Station in north Australia during the 2014 early dry season. This paper presents an overview of the fires in this region, the measurements of their emissions and the implications of these fires on the atmosphere.
Cliff S. Law, Murray J. Smith, Mike J. Harvey, Thomas G. Bell, Luke T. Cravigan, Fiona C. Elliott, Sarah J. Lawson, Martine Lizotte, Andrew Marriner, John McGregor, Zoran Ristovski, Karl A. Safi, Eric S. Saltzman, Petri Vaattovaara, and Carolyn F. Walker
Atmos. Chem. Phys., 17, 13645–13667, https://doi.org/10.5194/acp-17-13645-2017, https://doi.org/10.5194/acp-17-13645-2017, 2017
Short summary
Short summary
We carried out a multidisciplinary study to examine how aerosol production is influenced by the production and emission of trace gases and particles in the surface ocean. Phytoplankton blooms of different species composition in frontal waters southeast of New Zealand were a significant source of dimethylsulfide and other aerosol precursors. The relationships between surface ocean biogeochemistry and aerosol composition will inform the understanding of aerosol production over the remote ocean.
Sarah J. Lawson, Martin Cope, Sunhee Lee, Ian E. Galbally, Zoran Ristovski, and Melita D. Keywood
Atmos. Chem. Phys., 17, 11707–11726, https://doi.org/10.5194/acp-17-11707-2017, https://doi.org/10.5194/acp-17-11707-2017, 2017
Short summary
Short summary
A high-resolution chemical transport model was used to reproduce observed smoke plumes. The model output was highly sensitive to fire emission factors and meteorology, particularly for secondary pollutant ozone. Aged urban air (age = 2 days) was the major source of ozone observed, with minor contributions from the fire. This work highlights the importance of assessing model sensitivity and the use of modelling to determine the contribution from different sources to atmospheric composition.
Clare Paton-Walsh, Élise-Andrée Guérette, Dagmar Kubistin, Ruhi Humphries, Stephen R. Wilson, Doreena Dominick, Ian Galbally, Rebecca Buchholz, Mahendra Bhujel, Scott Chambers, Min Cheng, Martin Cope, Perry Davy, Kathryn Emmerson, David W. T. Griffith, Alan Griffiths, Melita Keywood, Sarah Lawson, Suzie Molloy, Géraldine Rea, Paul Selleck, Xue Shi, Jack Simmons, and Voltaire Velazco
Earth Syst. Sci. Data, 9, 349–362, https://doi.org/10.5194/essd-9-349-2017, https://doi.org/10.5194/essd-9-349-2017, 2017
Short summary
Short summary
The MUMBA campaign provides a detailed snapshot of the atmospheric composition in an urban coastal environment with strong biogenic sources nearby. This campaign involved collaboration between several institutes and was undertaken to provide a case study for atmospheric models in a poorly sampled region of the globe.
Andelija Milic, Marc D. Mallet, Luke T. Cravigan, Joel Alroe, Zoran D. Ristovski, Paul Selleck, Sarah J. Lawson, Jason Ward, Maximilien J. Desservettaz, Clare Paton-Walsh, Leah R. Williams, Melita D. Keywood, and Branka Miljevic
Atmos. Chem. Phys., 17, 3945–3961, https://doi.org/10.5194/acp-17-3945-2017, https://doi.org/10.5194/acp-17-3945-2017, 2017
Short summary
Short summary
This study reports chemical characterization of fresh and processed aerosols sampled over a month-long field campaign, during the intense fire period in Australian tropical savannah region. The study illustrates diversity in fire emissions and importance of processed fire emissions and formation of secondary species, including biogenic secondary species, in northern Australia.
Kathryn M. Emmerson, Ian E. Galbally, Alex B. Guenther, Clare Paton-Walsh, Elise-Andree Guerette, Martin E. Cope, Melita D. Keywood, Sarah J. Lawson, Suzie B. Molloy, Erin Dunne, Marcus Thatcher, Thomas Karl, and Simin D. Maleknia
Atmos. Chem. Phys., 16, 6997–7011, https://doi.org/10.5194/acp-16-6997-2016, https://doi.org/10.5194/acp-16-6997-2016, 2016
Short summary
Short summary
We have tested how a model using a global inventory of plant-based emissions compares with four sets of measurements made in southeast Australia. This region is known for its eucalypt species, which dominate the summertime global inventory. The Australian part of the inventory has been produced using measurements made on eucalypt saplings. The model could not match the measurements, and the inventory needs to be improved by taking measurements of a wider range of Australian plant types and ages.
S. J. Lawson, M. D. Keywood, I. E. Galbally, J. L. Gras, J. M. Cainey, M. E. Cope, P. B. Krummel, P. J. Fraser, L. P. Steele, S. T. Bentley, C. P. Meyer, Z. Ristovski, and A. H. Goldstein
Atmos. Chem. Phys., 15, 13393–13411, https://doi.org/10.5194/acp-15-13393-2015, https://doi.org/10.5194/acp-15-13393-2015, 2015
Short summary
Short summary
Biomass burning (BB) plumes were opportunistically measured at the Cape Grim Baseline Station in Tasmania, Australia. We provide a unique set of trace gas and particle emission factors for temperate Australian coastal heathland fires, and attribute a major short-lived enhancement in emission ratios to a minor rainfall event. The ability of BB particles to act as cloud condensation nuclei, and the contribution of BB emissions to observed particle growth and ozone enhancements are discussed.
S. J. Lawson, P. W. Selleck, I. E. Galbally, M. D. Keywood, M. J. Harvey, C. Lerot, D. Helmig, and Z. Ristovski
Atmos. Chem. Phys., 15, 223–240, https://doi.org/10.5194/acp-15-223-2015, https://doi.org/10.5194/acp-15-223-2015, 2015
Short summary
Short summary
Glyoxal and methylglyoxal are short-lived organic trace gases and important precursors of secondary organic aerosol. Measurements over oceans are sparse. We present the first in situ glyoxal and methylglyoxal observations over remote temperate oceans, alongside observations of precursor gases. Precursor gases cannot explain observed mixing ratios, highlighting an unknown source. We show a large discrepancy between calculated vertical column densities of glyoxal and those retrieved by satellite.
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.
Alexander T. Archibald, Bablu Sinha, Maria Russo, Emily Matthews, Freya Squires, N. Luke Abraham, Stephane Bauguitte, Thomas Bannan, Thomas Bell, David Berry, Lucy Carpenter, Hugh Coe, Andrew Coward, Peter Edwards, Daniel Feltham, Dwayne Heard, Jim Hopkins, James Keeble, Elizabeth C. Kent, Brian King, Isobel R. Lawrence, James Lee, Claire R. Macintosh, Alex Megann, Ben I. Moat, Katie Read, Chris Reed, Malcolm Roberts, Reinhard Schiemann, David Schroeder, Tim Smyth, Loren Temple, Navaneeth Thamban, Lisa Whalley, Simon Williams, Huihui Wu, and Ming-Xi Yang
Earth Syst. Sci. Data Discuss., https://doi.org/10.5194/essd-2023-405, https://doi.org/10.5194/essd-2023-405, 2024
Revised manuscript accepted for ESSD
Short summary
Short summary
Here we present an overview of the data generated as part of the North Atlantic Climate System Integrated Studies (ACSIS) programme which are available through dedicated repositories at the Centre for Environmental Data Analysis (CEDA, www.ceda.ac.uk) and the British Oceanographic Data Centre (BODC, bodc.ac.uk). ACSIS data cover the full North Atlantic System comprising: the North Atlantic Ocean, the atmosphere above it including its composition, Arctic Sea Ice and the Greenland Ice Sheet.
John D. Patterson, Murat Aydin, Andrew M. Crotwell, Gabrielle Pétron, Jeffery P. Severinghaus, Paul B. Krummel, Ray L. Langenfelds, Vasilii V. Petrenko, and Eric S. Saltzman
Clim. Past, 19, 2535–2550, https://doi.org/10.5194/cp-19-2535-2023, https://doi.org/10.5194/cp-19-2535-2023, 2023
Short summary
Short summary
Atmospheric levels of molecular hydrogen (H2) can impact climate and air quality. Constraining past changes to atmospheric H2 is useful for understanding how H2 cycles through the Earth system and predicting the impacts of increasing anthropogenic emissions under the
hydrogen economy. Here, we use the aging air found in the polar snowpack to reconstruct H2 levels over the past 100 years. We find that H2 levels increased by 30 % over Greenland and 60 % over Antarctica during the 20th century.
Karine Sellegri, Theresa Barthelmeß, Jonathan Trueblood, Antonia Cristi, Evelyn Freney, Clémence Rose, Neill Barr, Mike Harvey, Karl Safi, Stacy Deppeler, Karen Thompson, Wayne Dillon, Anja Engel, and Cliff Law
Atmos. Chem. Phys., 23, 12949–12964, https://doi.org/10.5194/acp-23-12949-2023, https://doi.org/10.5194/acp-23-12949-2023, 2023
Short summary
Short summary
The amount of sea spray emitted to the atmosphere depends on the ocean temperature, but this dependency is not well understood, especially when ocean biology is involved. In this study, we show that sea spray emissions are increased by up to a factor of 4 at low seawater temperatures compared to moderate temperatures, and we quantify the temperature dependence as a function of the ocean biogeochemistry.
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
Short summary
Short summary
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.
Manon Rocco, Erin Dunne, Alexia Saint-Macary, Maija Peltola, Theresa Barthelmeß, Neill Barr, Karl Safi, Andrew Marriner, Stacy Deppeler, James Harnwell, Anja Engel, Aurélie Colomb, Alfonso Saiz-Lopez, Mike Harvey, Cliff S. Law, and Karine Sellegri
EGUsphere, https://doi.org/10.5194/egusphere-2023-516, https://doi.org/10.5194/egusphere-2023-516, 2023
Preprint archived
Short summary
Short summary
During the Sea2cloud campaign in the Southern Pacific Ocean, we measured air-sea emissions from phytopankton of two key atmospheric compounds: DMS and MeSH. These compounds are well-known to play a great role in atmospheric chemistry and climate. We see in this paper that these compounds are most emited by the nanophytoplankton population. We provide here parameters for climate models to predict future trends of the emissions of these compounds and their roles and impacts on the global warming.
Maija Peltola, Clémence Rose, Jonathan V. Trueblood, Sally Gray, Mike Harvey, and Karine Sellegri
Atmos. Chem. Phys., 23, 3955–3983, https://doi.org/10.5194/acp-23-3955-2023, https://doi.org/10.5194/acp-23-3955-2023, 2023
Short summary
Short summary
We measured the chemical composition of ambient ions at a coastal New Zealand site and connected these data with aerosol size distribution data to study the chemical precursors of new particle formation at the site. Our results showed that iodine oxides and sulfur species were important for particle formation in marine air, while in land-influenced air sulfuric acid and organics were connected to new particle formation events.
Veronica Z. Berta, Lynn M. Russell, Derek J. Price, Chia-Li Chen, Alex K. Y. Lee, Patricia K. Quinn, Timothy S. Bates, Thomas G. Bell, and Michael J. Behrenfeld
Atmos. Chem. Phys., 23, 2765–2787, https://doi.org/10.5194/acp-23-2765-2023, https://doi.org/10.5194/acp-23-2765-2023, 2023
Short summary
Short summary
Amines are compounds emitted from a variety of marine and continental sources and were measured by aerosol mass spectrometry and Fourier transform infrared spectroscopy during the North Atlantic Aerosols and Marine Ecosystems Study (NAAMES) cruises. Secondary continental and primary marine sources of amines were identified by comparisons to tracers. The results show that the two methods are complementary for investigating amines in the marine environment.
Alexia D. Saint-Macary, Andrew Marriner, Theresa Barthelmeß, Stacy Deppeler, Karl Safi, Rafael Costa Santana, Mike Harvey, and Cliff S. Law
Ocean Sci., 19, 1–15, https://doi.org/10.5194/os-19-1-2023, https://doi.org/10.5194/os-19-1-2023, 2023
Short summary
Short summary
The uppermost oceanic layer was sampled to determine what can explain a potential dimethyl sulfide (DMS) enrichment in this environment. A novel sampling method was used, and the results showed that DMS was not as enriched as expected. Our results showed that the phytoplanktonic composition influenced the DMS concentration, confirming results from another study in this oceanic region. However, additional factors are required to observe a DMS enrichment in the uppermost oceanic layer.
Alexia D. Saint-Macary, Andrew Marriner, Stacy Deppeler, Karl A. Safi, and Cliff S. Law
Ocean Sci., 18, 1559–1571, https://doi.org/10.5194/os-18-1559-2022, https://doi.org/10.5194/os-18-1559-2022, 2022
Short summary
Short summary
To understand how dimethyl sulfide (DMS) enrichment is maintained in the sea surface microlayer (SML) while DMS is lost to the atmosphere, deck-board incubation was carried out to determine DMS sources and sinks. Our results showed that the phytoplankton composition played an essential role in DMS processes in the SML. However, all accumulated DMS processes were lower than the calculated air–sea DMS flux.
Shrivardhan Hulswar, Rafel Simó, Martí Galí, Thomas G. Bell, Arancha Lana, Swaleha Inamdar, Paul R. Halloran, George Manville, and Anoop Sharad Mahajan
Earth Syst. Sci. Data, 14, 2963–2987, https://doi.org/10.5194/essd-14-2963-2022, https://doi.org/10.5194/essd-14-2963-2022, 2022
Short summary
Short summary
The third climatological estimation of sea surface dimethyl sulfide (DMS) concentrations based on in situ measurements was created (DMS-Rev3). The update includes a much larger input dataset and includes improvements in the data unification, filtering, and smoothing algorithm. The DMS-Rev3 climatology provides more realistic monthly estimates of DMS, and shows significant regional differences compared to past climatologies.
Maija Peltola, Clémence Rose, Jonathan V. Trueblood, Sally Gray, Mike Harvey, and Karine Sellegri
Atmos. Chem. Phys., 22, 6231–6254, https://doi.org/10.5194/acp-22-6231-2022, https://doi.org/10.5194/acp-22-6231-2022, 2022
Short summary
Short summary
Despite the importance of marine aerosol measurements for constraining climate models, these measurements are scarce. We measured the aerosol particle number size distribution in coastal New Zealand over a total period of 10 months. This paper analyses the aerosol properties at the site, with a special focus on new particle formation and marine air masses. New particle formation was observed frequently, but in marine air masses it did not follow traditional event criteria.
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
Short summary
Short summary
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.
Kevin J. Sanchez, Bo Zhang, Hongyu Liu, Matthew D. Brown, Ewan C. Crosbie, Francesca Gallo, Johnathan W. Hair, Chris A. Hostetler, Carolyn E. Jordan, Claire E. Robinson, Amy Jo Scarino, Taylor J. Shingler, Michael A. Shook, Kenneth L. Thornhill, Elizabeth B. Wiggins, Edward L. Winstead, Luke D. Ziemba, Georges Saliba, Savannah L. Lewis, Lynn M. Russell, Patricia K. Quinn, Timothy S. Bates, Jack Porter, Thomas G. Bell, Peter Gaube, Eric S. Saltzman, Michael J. Behrenfeld, and Richard H. Moore
Atmos. Chem. Phys., 22, 2795–2815, https://doi.org/10.5194/acp-22-2795-2022, https://doi.org/10.5194/acp-22-2795-2022, 2022
Short summary
Short summary
Atmospheric particle concentrations impact clouds, which strongly impact the amount of sunlight reflected back into space and the overall climate. Measurements of particles over the ocean are rare and expensive to collect, so models are necessary to fill in the gaps by simulating both particle and clouds. However, some measurements are needed to test the accuracy of the models. Here, we measure changes in particles in different weather conditions, which are ideal for comparison with models.
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
Short summary
Short summary
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 P. Phillips, Frances E. Hopkins, Thomas G. Bell, Peter S. Liss, Philip D. Nightingale, Claire E. Reeves, Charel Wohl, and Mingxi Yang
Atmos. Chem. Phys., 21, 10111–10132, https://doi.org/10.5194/acp-21-10111-2021, https://doi.org/10.5194/acp-21-10111-2021, 2021
Short summary
Short summary
We present the first measurements of the rate of transfer (flux) of three gases between the atmosphere and the ocean, using a direct flux measurement technique, at a coastal site. We show greater atmospheric loss of acetone and acetaldehyde into the ocean than estimated by global models for the open water; importantly, the acetaldehyde transfer direction is opposite to the model estimates. Measured dimethylsulfide fluxes agreed with a recent model. Isoprene fluxes were too weak to be measured.
Stefanie Kremser, Mike Harvey, Peter Kuma, Sean Hartery, Alexia Saint-Macary, John McGregor, Alex Schuddeboom, Marc von Hobe, Sinikka T. Lennartz, Alex Geddes, Richard Querel, Adrian McDonald, Maija Peltola, Karine Sellegri, Israel Silber, Cliff S. Law, Connor J. Flynn, Andrew Marriner, Thomas C. J. Hill, Paul J. DeMott, Carson C. Hume, Graeme Plank, Geoffrey Graham, and Simon Parsons
Earth Syst. Sci. Data, 13, 3115–3153, https://doi.org/10.5194/essd-13-3115-2021, https://doi.org/10.5194/essd-13-3115-2021, 2021
Short summary
Short summary
Aerosol–cloud interactions over the Southern Ocean are poorly understood and remain a major source of uncertainty in climate models. This study presents ship-borne measurements, collected during a 6-week voyage into the Southern Ocean in 2018, that are an important supplement to satellite-based measurements. For example, these measurements include data on low-level clouds and aerosol composition in the marine boundary layer, which can be used in climate model evaluation efforts.
Yuanxu Dong, Mingxi Yang, Dorothee C. E. Bakker, Vassilis Kitidis, and Thomas G. Bell
Atmos. Chem. Phys., 21, 8089–8110, https://doi.org/10.5194/acp-21-8089-2021, https://doi.org/10.5194/acp-21-8089-2021, 2021
Short summary
Short summary
Eddy covariance (EC) is the most direct method for measuring air–sea CO2 flux from ships. However, uncertainty in EC air–sea CO2 fluxes has not been well quantified. Here we show that with the state-of-the-art gas analysers, instrumental noise no longer contributes significantly to the CO2 flux uncertainty. Applying an appropriate averaging timescale (1–3 h) and suitable air–sea CO2 fugacity threshold (at least 20 µatm) to EC flux data enables an optimal analysis of the gas transfer velocity.
Kevin J. Sanchez, Bo Zhang, Hongyu Liu, Georges Saliba, Chia-Li Chen, Savannah L. Lewis, Lynn M. Russell, Michael A. Shook, Ewan C. Crosbie, Luke D. Ziemba, Matthew D. Brown, Taylor J. Shingler, Claire E. Robinson, Elizabeth B. Wiggins, Kenneth L. Thornhill, Edward L. Winstead, Carolyn Jordan, Patricia K. Quinn, Timothy S. Bates, Jack Porter, Thomas G. Bell, Eric S. Saltzman, Michael J. Behrenfeld, and Richard H. Moore
Atmos. Chem. Phys., 21, 831–851, https://doi.org/10.5194/acp-21-831-2021, https://doi.org/10.5194/acp-21-831-2021, 2021
Short summary
Short summary
Models describing atmospheric airflow were combined with satellite measurements representative of marine phytoplankton and other meteorological variables. These combined variables were compared to measured aerosol to identify upwind influences on aerosol concentrations. Results indicate that phytoplankton production rates upwind impact the aerosol mass. Also, results suggest that the condensation of mass onto short-lived large sea spray particles may be a significant sink of aerosol mass.
Michael J. Lawler, Savannah L. Lewis, Lynn M. Russell, Patricia K. Quinn, Timothy S. Bates, Derek J. Coffman, Lucia M. Upchurch, and Eric S. Saltzman
Atmos. Chem. Phys., 20, 16007–16022, https://doi.org/10.5194/acp-20-16007-2020, https://doi.org/10.5194/acp-20-16007-2020, 2020
Short summary
Short summary
This work describes new measurements of aerosol (particles) composition over the North Atlantic Ocean. It provides concentrations of polysaccharide material likely made from organisms in the surface ocean and improves our understanding of the relative importance of such fresh biogenic material compared to more recalcitrant organic carbon in forming marine organic aerosol. We aim ultimately to understand the role that ocean biology plays in cloud formation in marine regions.
David C. Loades, Mingxi Yang, Thomas G. Bell, Adam R. Vaughan, Ryan J. Pound, Stefan Metzger, James D. Lee, and Lucy J. Carpenter
Atmos. Meas. Tech., 13, 6915–6931, https://doi.org/10.5194/amt-13-6915-2020, https://doi.org/10.5194/amt-13-6915-2020, 2020
Short summary
Short summary
The loss of ozone to the sea surface was measured from the south coast of the UK and was found to be more rapid than previous observations over the open ocean. This is likely a consequence of different chemistry and biology in coastal environments. Strong winds appeared to speed up the loss of ozone. A better understanding of what influences ozone loss over the sea will lead to better model estimates of total ozone in the troposphere.
André Welti, E. Keith Bigg, Paul J. DeMott, Xianda Gong, Markus Hartmann, Mike Harvey, Silvia Henning, Paul Herenz, Thomas C. J. Hill, Blake Hornblow, Caroline Leck, Mareike Löffler, Christina S. McCluskey, Anne Marie Rauker, Julia Schmale, Christian Tatzelt, Manuela van Pinxteren, and Frank Stratmann
Atmos. Chem. Phys., 20, 15191–15206, https://doi.org/10.5194/acp-20-15191-2020, https://doi.org/10.5194/acp-20-15191-2020, 2020
Short summary
Short summary
Ship-based measurements of maritime ice nuclei concentrations encompassing all oceans are compiled. From this overview it is found that maritime ice nuclei concentrations are typically 10–100 times lower than over continents, while concentrations are surprisingly similar in different oceanic regions. The analysis of the influence of ship emissions shows no effect on the data, making ship-based measurements an efficient strategy for the large-scale exploration of ice nuclei concentrations.
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
Short summary
Short summary
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.
Luke T. Cravigan, Marc D. Mallet, Petri Vaattovaara, Mike J. Harvey, Cliff S. Law, Robin L. Modini, Lynn M. Russell, Ed Stelcer, David D. Cohen, Greg Olsen, Karl Safi, Timothy J. Burrell, and Zoran Ristovski
Atmos. Chem. Phys., 20, 7955–7977, https://doi.org/10.5194/acp-20-7955-2020, https://doi.org/10.5194/acp-20-7955-2020, 2020
Short summary
Short summary
Aerosol–cloud interactions in remote marine environments are poorly represented in atmospheric modelling, particularly over the Southern Hemisphere. This work reports in situ chamber observations of sea spray aerosol composition and water uptake during the Surface Ocean Aerosol Production (SOAP) voyage. Observations were compared with currently applied models for sea spray organic enrichment. The sea spray hygroscopicity was persistently high, even at high organic fractions.
Peter Kuma, Adrian J. McDonald, Olaf Morgenstern, Simon P. Alexander, John J. Cassano, Sally Garrett, Jamie Halla, Sean Hartery, Mike J. Harvey, Simon Parsons, Graeme Plank, Vidya Varma, and Jonny Williams
Atmos. Chem. Phys., 20, 6607–6630, https://doi.org/10.5194/acp-20-6607-2020, https://doi.org/10.5194/acp-20-6607-2020, 2020
Short summary
Short summary
We evaluate clouds over the Southern Ocean in the climate model HadGEM3 and reanalysis MERRA-2 using ship-based ceilometer and radiosonde observations. We find the models underestimate cloud cover by 18–25 %, with clouds below 2 km dominant in reality but lacking in the models. We find a strong link between clouds, atmospheric stability and sea surface temperature in observations but not in the models, implying that sub-grid processes do not generate enough cloud in response to these conditions.
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
Short summary
Short summary
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.
Laura E. Revell, Stefanie Kremser, Sean Hartery, Mike Harvey, Jane P. Mulcahy, Jonny Williams, Olaf Morgenstern, Adrian J. McDonald, Vidya Varma, Leroy Bird, and Alex Schuddeboom
Atmos. Chem. Phys., 19, 15447–15466, https://doi.org/10.5194/acp-19-15447-2019, https://doi.org/10.5194/acp-19-15447-2019, 2019
Short summary
Short summary
Aerosols over the Southern Ocean consist primarily of sea salt and sulfate, yet are seasonally biased in our model. We test three sulfate chemistry schemes to investigate DMS oxidation, which forms sulfate aerosol. Simulated cloud droplet number concentrations improve using more complex sulfate chemistry. We also show that a new sea spray aerosol source function, developed from measurements made on a recent Southern Ocean research voyage, improves the model's simulation of aerosol optical depth.
Mingxi Yang, Sarah J. Norris, Thomas G. Bell, and Ian M. Brooks
Atmos. Chem. Phys., 19, 15271–15284, https://doi.org/10.5194/acp-19-15271-2019, https://doi.org/10.5194/acp-19-15271-2019, 2019
Short summary
Short summary
This work reports direct measurements of sea spray fluxes from a coastal site in the UK, which are relevant for atmospheric chemistry as well as coastal air quality. Sea spray fluxes from this location are roughly an order of magnitude greater than over the open ocean at similar wind conditions, comparable to previous coastal measurements. Unlike previous open ocean measurements that are largely wind speed dependent, we find that sea spray fluxes near the coast depend more strongly on waves.
Melita Keywood, Paul Selleck, Fabienne Reisen, David Cohen, Scott Chambers, Min Cheng, Martin Cope, Suzanne Crumeyrolle, Erin Dunne, Kathryn Emmerson, Rosemary Fedele, Ian Galbally, Rob Gillett, Alan Griffiths, Elise-Andree Guerette, James Harnwell, Ruhi Humphries, Sarah Lawson, Branka Miljevic, Suzie Molloy, Jennifer Powell, Jack Simmons, Zoran Ristovski, and Jason Ward
Earth Syst. Sci. Data, 11, 1883–1903, https://doi.org/10.5194/essd-11-1883-2019, https://doi.org/10.5194/essd-11-1883-2019, 2019
Short summary
Short summary
The Sydney Particle Study increased scientific knowledge of the processes leading to particle formation and transformations in Sydney through two comprehensive observation programs which are described in detail here. The data set and its analysis underpin comprehensive chemical transport modelling tools that can be used to assist in the development of a long-term control strategy for particles in Sydney and thus reduce the impact of particles on human health.
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
Short summary
Short summary
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.
Jack G. Porter, Warren De Bruyn, and Eric S. Saltzman
Atmos. Chem. Phys., 18, 15291–15305, https://doi.org/10.5194/acp-18-15291-2018, https://doi.org/10.5194/acp-18-15291-2018, 2018
Short summary
Short summary
Deposition to the sea surface is a major loss pathway for highly soluble atmospheric trace gases. These fluxes are important to biogeochemical cycles, climate, and air quality. Here we report measurements of air–sea fluxes of sulfur dioxide, sensible heat, and momentum to coastal waters. Transfer velocities derived from the data show a dependence on molecular diffusivity, demonstrating the importance of diffusion in the interfacial layer on the atmospheric side of the air–sea interface.
Samuel T. Wilson, Hermann W. Bange, Damian L. Arévalo-Martínez, Jonathan Barnes, Alberto V. Borges, Ian Brown, John L. Bullister, Macarena Burgos, David W. Capelle, Michael Casso, Mercedes de la Paz, Laura Farías, Lindsay Fenwick, Sara Ferrón, Gerardo Garcia, Michael Glockzin, David M. Karl, Annette Kock, Sarah Laperriere, Cliff S. Law, Cara C. Manning, Andrew Marriner, Jukka-Pekka Myllykangas, John W. Pohlman, Andrew P. Rees, Alyson E. Santoro, Philippe D. Tortell, Robert C. Upstill-Goddard, David P. Wisegarver, Gui-Ling Zhang, and Gregor Rehder
Biogeosciences, 15, 5891–5907, https://doi.org/10.5194/bg-15-5891-2018, https://doi.org/10.5194/bg-15-5891-2018, 2018
Short summary
Short summary
To determine the variability between independent measurements of dissolved methane and nitrous oxide, seawater samples were analyzed by multiple laboratories. The results revealed the influences of the different parts of the analytical process, from the initial sample collection to the calculation of the final concentrations. Recommendations are made to improve dissolved methane and nitrous oxide measurements to help preclude future analytical discrepancies between laboratories.
Murray J. Smith, Carolyn F. Walker, Thomas G. Bell, Mike J. Harvey, Eric S. Saltzman, and Cliff S. Law
Atmos. Chem. Phys., 18, 5861–5877, https://doi.org/10.5194/acp-18-5861-2018, https://doi.org/10.5194/acp-18-5861-2018, 2018
Short summary
Short summary
The transfer of gases across the air–sea interface has a significant influence on climate. During a research voyage in the South Pacific we measured the transfer rate of the biogenic gas dimethyl sulfide (DMS) from the ocean using two independent methods. The agreement between the techniques provides confidence in their use in compilations of global gas transfer. We also identified physical conditions under which the observations are not well predicted by a standard gas transfer model.
Sebastian Landwehr, Scott D. Miller, Murray J. Smith, Thomas G. Bell, Eric S. Saltzman, and Brian Ward
Atmos. Chem. Phys., 18, 4297–4315, https://doi.org/10.5194/acp-18-4297-2018, https://doi.org/10.5194/acp-18-4297-2018, 2018
Short summary
Short summary
The ocean takes up about 25 % of emitted anthropogenic emitted carbon dioxide and thus plays a significant role in the regulation of climate. In order to accurately calculate this uptake, a quantity known as the air–sea gas transfer velocity needs to be determined. This is typically parameterised with mean wind speed, the most commonly used velocity scale for calculating air–sea transfer coefficients. In this article, we propose an alternative velocity scale known as the friction velocity.
Yuanyuan Feng, Michael Y. Roleda, Evelyn Armstrong, Cliff S. Law, Philip W. Boyd, and Catriona L. Hurd
Biogeosciences, 15, 581–595, https://doi.org/10.5194/bg-15-581-2018, https://doi.org/10.5194/bg-15-581-2018, 2018
Short summary
Short summary
We conducted a series of incubation experiments to understand how the changes in five environmental drivers will affect the elemental composition of the calcifying phytoplankton species Emiliania huxleyi. These findings provide new diagnostic information to aid our understanding of how the physiology and the related marine biogeochemistry of the ecologically important species Emiliania huxleyi will respond to changes in different environmental drivers in the global climate change scenario.
Erin Dunne, Ian E. Galbally, Min Cheng, Paul Selleck, Suzie B. Molloy, and Sarah J. Lawson
Atmos. Meas. Tech., 11, 141–159, https://doi.org/10.5194/amt-11-141-2018, https://doi.org/10.5194/amt-11-141-2018, 2018
Short summary
Short summary
A comparison of measurements of 7 volatile organic compounds (VOCs) in urban air by 3 different methods is presented. An uncertainty was calculated for each method and VOCs measured to provide some idea of the reliability of the data. Even when this uncertainty was accounted for, the measurements from the different methods did not agree for 4 of the 7 VOCs. Thus, there is unaccounted uncertainty in VOC measurements which must be considered when utilizing the data and assessing their reliability.
Martine Lizotte, Maurice Levasseur, Cliff S. Law, Carolyn F. Walker, Karl A. Safi, Andrew Marriner, and Ronald P. Kiene
Ocean Sci., 13, 961–982, https://doi.org/10.5194/os-13-961-2017, https://doi.org/10.5194/os-13-961-2017, 2017
Short summary
Short summary
During a 4-week oceanographic cruise in 2012, we investigated the water masses bordering the subtropical front near New Zealand as sources of the biogenic gas dimethyl sulfide (DMS). DMS oxidation products may influence the atmospheric radiative budget of the Earth. Concentrations of DMS were high in the study region and DMS's precursor, dimethylsulfoniopropionate, showed a strong association with phytoplankton biomass in relation to the persistent dominance of dinoflagellates/coccolithophores.
Marc D. Mallet, Maximilien J. Desservettaz, Branka Miljevic, Andelija Milic, Zoran D. Ristovski, Joel Alroe, Luke T. Cravigan, E. Rohan Jayaratne, Clare Paton-Walsh, David W. T. Griffith, Stephen R. Wilson, Graham Kettlewell, Marcel V. van der Schoot, Paul Selleck, Fabienne Reisen, Sarah J. Lawson, Jason Ward, James Harnwell, Min Cheng, Rob W. Gillett, Suzie B. Molloy, Dean Howard, Peter F. Nelson, Anthony L. Morrison, Grant C. Edwards, Alastair G. Williams, Scott D. Chambers, Sylvester Werczynski, Leah R. Williams, V. Holly L. Winton, Brad Atkinson, Xianyu Wang, and Melita D. Keywood
Atmos. Chem. Phys., 17, 13681–13697, https://doi.org/10.5194/acp-17-13681-2017, https://doi.org/10.5194/acp-17-13681-2017, 2017
Short summary
Short summary
Fires play an important role within atmosphere. Gaseous and aerosol emissions influence Earth's temperature but these emissions can vary drastically across region and season. The SAFIRED (Savannah Fires in the Early Dry Season) campaign was undertaken at the Australian Tropical Research Station in north Australia during the 2014 early dry season. This paper presents an overview of the fires in this region, the measurements of their emissions and the implications of these fires on the atmosphere.
Cliff S. Law, Murray J. Smith, Mike J. Harvey, Thomas G. Bell, Luke T. Cravigan, Fiona C. Elliott, Sarah J. Lawson, Martine Lizotte, Andrew Marriner, John McGregor, Zoran Ristovski, Karl A. Safi, Eric S. Saltzman, Petri Vaattovaara, and Carolyn F. Walker
Atmos. Chem. Phys., 17, 13645–13667, https://doi.org/10.5194/acp-17-13645-2017, https://doi.org/10.5194/acp-17-13645-2017, 2017
Short summary
Short summary
We carried out a multidisciplinary study to examine how aerosol production is influenced by the production and emission of trace gases and particles in the surface ocean. Phytoplankton blooms of different species composition in frontal waters southeast of New Zealand were a significant source of dimethylsulfide and other aerosol precursors. The relationships between surface ocean biogeochemistry and aerosol composition will inform the understanding of aerosol production over the remote ocean.
Sarah J. Lawson, Martin Cope, Sunhee Lee, Ian E. Galbally, Zoran Ristovski, and Melita D. Keywood
Atmos. Chem. Phys., 17, 11707–11726, https://doi.org/10.5194/acp-17-11707-2017, https://doi.org/10.5194/acp-17-11707-2017, 2017
Short summary
Short summary
A high-resolution chemical transport model was used to reproduce observed smoke plumes. The model output was highly sensitive to fire emission factors and meteorology, particularly for secondary pollutant ozone. Aged urban air (age = 2 days) was the major source of ozone observed, with minor contributions from the fire. This work highlights the importance of assessing model sensitivity and the use of modelling to determine the contribution from different sources to atmospheric composition.
Richard P. Sims, Ute Schuster, Andrew J. Watson, Ming Xi Yang, Frances E. Hopkins, John Stephens, and Thomas G. Bell
Ocean Sci., 13, 649–660, https://doi.org/10.5194/os-13-649-2017, https://doi.org/10.5194/os-13-649-2017, 2017
Short summary
Short summary
This paper describes a near-surface ocean profiler (NSOP) that is deployed from a research vessel. The NSOP is used to sample the top 10 m of the ocean and pumps water back to the research ship for scientific analyses such as for trace gases. The precision in the depth of the seawater collection improves upon previous methods. The NSOP has been used to observe vertical gradients in the upper 5 m for temperature, carbon dioxide and dimethylsulfide.
Thomas G. Bell, Sebastian Landwehr, Scott D. Miller, Warren J. de Bruyn, Adrian H. Callaghan, Brian Scanlon, Brian Ward, Mingxi Yang, and Eric S. Saltzman
Atmos. Chem. Phys., 17, 9019–9033, https://doi.org/10.5194/acp-17-9019-2017, https://doi.org/10.5194/acp-17-9019-2017, 2017
Short summary
Short summary
The mechanisms that determine the air–sea exchange of gases such as carbon dioxide are not well understood. During a research cruise in the North Atlantic, we simultaneously measured the air–sea transfer of two gases with contrasting solubility over a range in wind and wave conditions. We compare the transfer of these gases to improve understanding of how bubbles from breaking waves may mediate air–sea gas fluxes.
Clare Paton-Walsh, Élise-Andrée Guérette, Dagmar Kubistin, Ruhi Humphries, Stephen R. Wilson, Doreena Dominick, Ian Galbally, Rebecca Buchholz, Mahendra Bhujel, Scott Chambers, Min Cheng, Martin Cope, Perry Davy, Kathryn Emmerson, David W. T. Griffith, Alan Griffiths, Melita Keywood, Sarah Lawson, Suzie Molloy, Géraldine Rea, Paul Selleck, Xue Shi, Jack Simmons, and Voltaire Velazco
Earth Syst. Sci. Data, 9, 349–362, https://doi.org/10.5194/essd-9-349-2017, https://doi.org/10.5194/essd-9-349-2017, 2017
Short summary
Short summary
The MUMBA campaign provides a detailed snapshot of the atmospheric composition in an urban coastal environment with strong biogenic sources nearby. This campaign involved collaboration between several institutes and was undertaken to provide a case study for atmospheric models in a poorly sampled region of the globe.
Andelija Milic, Marc D. Mallet, Luke T. Cravigan, Joel Alroe, Zoran D. Ristovski, Paul Selleck, Sarah J. Lawson, Jason Ward, Maximilien J. Desservettaz, Clare Paton-Walsh, Leah R. Williams, Melita D. Keywood, and Branka Miljevic
Atmos. Chem. Phys., 17, 3945–3961, https://doi.org/10.5194/acp-17-3945-2017, https://doi.org/10.5194/acp-17-3945-2017, 2017
Short summary
Short summary
This study reports chemical characterization of fresh and processed aerosols sampled over a month-long field campaign, during the intense fire period in Australian tropical savannah region. The study illustrates diversity in fire emissions and importance of processed fire emissions and formation of secondary species, including biogenic secondary species, in northern Australia.
Mingxi Yang, John Prytherch, Elena Kozlova, Margaret J. Yelland, Deepulal Parenkat Mony, and Thomas G. Bell
Atmos. Meas. Tech., 9, 5509–5522, https://doi.org/10.5194/amt-9-5509-2016, https://doi.org/10.5194/amt-9-5509-2016, 2016
Short summary
Short summary
The exchange of the greenhouse gases carbon dioxide and methane between the ocean and the atmosphere is of critical importance for the earth's climate. Despite this, direct measurements of these fluxes are relatively scarce, especially for methane, in large part due to instrumental challenges. In this paper, we evaluate the performance of two of the latest carbon dioxide and methane flux analysers. We also compare their detection limits to predicted air–sea fluxes of these gases.
Carolyn F. Walker, Mike J. Harvey, Murray J. Smith, Thomas G. Bell, Eric S. Saltzman, Andrew S. Marriner, John A. McGregor, and Cliff S. Law
Ocean Sci., 12, 1033–1048, https://doi.org/10.5194/os-12-1033-2016, https://doi.org/10.5194/os-12-1033-2016, 2016
Timothy J. Burrell, Elizabeth W. Maas, Paul Teesdale-Spittle, and Cliff S. Law
Biogeosciences, 13, 4379–4388, https://doi.org/10.5194/bg-13-4379-2016, https://doi.org/10.5194/bg-13-4379-2016, 2016
Short summary
Short summary
Bacterial extracellular enzymes play a significant role in the degradation of organic matter in the open ocean. Using artificial fluorogenic substrates, this research highlights potential artefacts in the response of bacterial glucosidase and aminopeptidase to ocean acidification, and the effects of three different acidification techniques. We conclude that fluorogenic substrate degradation is affected by, or alters pH, and bubbling CO2 may lead to the overestimation of carbohydrate degradation.
Kathryn M. Emmerson, Ian E. Galbally, Alex B. Guenther, Clare Paton-Walsh, Elise-Andree Guerette, Martin E. Cope, Melita D. Keywood, Sarah J. Lawson, Suzie B. Molloy, Erin Dunne, Marcus Thatcher, Thomas Karl, and Simin D. Maleknia
Atmos. Chem. Phys., 16, 6997–7011, https://doi.org/10.5194/acp-16-6997-2016, https://doi.org/10.5194/acp-16-6997-2016, 2016
Short summary
Short summary
We have tested how a model using a global inventory of plant-based emissions compares with four sets of measurements made in southeast Australia. This region is known for its eucalypt species, which dominate the summertime global inventory. The Australian part of the inventory has been produced using measurements made on eucalypt saplings. The model could not match the measurements, and the inventory needs to be improved by taking measurements of a wider range of Australian plant types and ages.
Mingxi Yang, Thomas G. Bell, Frances E. Hopkins, Vassilis Kitidis, Pierre W. Cazenave, Philip D. Nightingale, Margaret J. Yelland, Robin W. Pascal, John Prytherch, Ian M. Brooks, and Timothy J. Smyth
Atmos. Chem. Phys., 16, 5745–5761, https://doi.org/10.5194/acp-16-5745-2016, https://doi.org/10.5194/acp-16-5745-2016, 2016
Short summary
Short summary
Coastal seas are sources of methane in the atmosphere and can fluctuate from emitting to absorbing carbon dioxide. Direct air–sea transport measurements of these two greenhouse gases in near shore regions remain scarce. From a recently established coastal atmospheric station on the south-west coast of the UK, we observed that the oceanic absorption of carbon dioxide peaked during the phytoplankton bloom, while methane emission varied with the tidal cycle, likely due to an estuary influence.
Mingxi Yang, Thomas G. Bell, Frances E. Hopkins, and Timothy J. Smyth
Atmos. Chem. Phys., 16, 4771–4783, https://doi.org/10.5194/acp-16-4771-2016, https://doi.org/10.5194/acp-16-4771-2016, 2016
Short summary
Short summary
Exhausts from ships are an important source of air pollution in coastal regions. We observed a ~ 3 fold reduction in the level of sulfur dioxide (a principle pollutant) from the English Channel from 2014 to 2015 after the new International Maritime Organisation regulation on ship sulfur emission became law. Our estimated ship's fuel sulfur content shows a high degree of compliance. Dimethylsulfide from the marine biota becomes a relatively more important source of sulfur in coastal marine air.
S. J. Lawson, M. D. Keywood, I. E. Galbally, J. L. Gras, J. M. Cainey, M. E. Cope, P. B. Krummel, P. J. Fraser, L. P. Steele, S. T. Bentley, C. P. Meyer, Z. Ristovski, and A. H. Goldstein
Atmos. Chem. Phys., 15, 13393–13411, https://doi.org/10.5194/acp-15-13393-2015, https://doi.org/10.5194/acp-15-13393-2015, 2015
Short summary
Short summary
Biomass burning (BB) plumes were opportunistically measured at the Cape Grim Baseline Station in Tasmania, Australia. We provide a unique set of trace gas and particle emission factors for temperate Australian coastal heathland fires, and attribute a major short-lived enhancement in emission ratios to a minor rainfall event. The ability of BB particles to act as cloud condensation nuclei, and the contribution of BB emissions to observed particle growth and ozone enhancements are discussed.
T. J. Burrell, E. W. Maas, P. Teesdale-Spittle, and C. S. Law
Biogeosciences Discuss., https://doi.org/10.5194/bgd-12-5841-2015, https://doi.org/10.5194/bgd-12-5841-2015, 2015
Manuscript not accepted for further review
Short summary
Short summary
pH has a significant effect on the artificial fluorophore for glucosidase and protease activity, while artificial aminopeptidase substrate alters the pH of seawater. Reduction of coastal seawater pH to 7.8 was shown to increase β-glucosidase activity rapidly (0.5h), while no significant response was detected for leucine aminopeptidase. Seawater acidified by bubbling CO2 gas resulted in elevated β-glucosidase activity and bacterial cell numbers, although seasonal effects were observed.
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
S. J. Lawson, P. W. Selleck, I. E. Galbally, M. D. Keywood, M. J. Harvey, C. Lerot, D. Helmig, and Z. Ristovski
Atmos. Chem. Phys., 15, 223–240, https://doi.org/10.5194/acp-15-223-2015, https://doi.org/10.5194/acp-15-223-2015, 2015
Short summary
Short summary
Glyoxal and methylglyoxal are short-lived organic trace gases and important precursors of secondary organic aerosol. Measurements over oceans are sparse. We present the first in situ glyoxal and methylglyoxal observations over remote temperate oceans, alongside observations of precursor gases. Precursor gases cannot explain observed mixing ratios, highlighting an unknown source. We show a large discrepancy between calculated vertical column densities of glyoxal and those retrieved by satellite.
A. M. S. McMillan, M. J. Harvey, R. J. Martin, A. M. Bromley, M. J. Evans, S. Mukherjee, and J. Laubach
Atmos. Meas. Tech., 7, 1169–1184, https://doi.org/10.5194/amt-7-1169-2014, https://doi.org/10.5194/amt-7-1169-2014, 2014
M. J. Lawler, A. S. Mahajan, A. Saiz-Lopez, and E. S. Saltzman
Atmos. Chem. Phys., 14, 2669–2678, https://doi.org/10.5194/acp-14-2669-2014, https://doi.org/10.5194/acp-14-2669-2014, 2014
T. G. Bell, W. De Bruyn, S. D. Miller, B. Ward, K. H. Christensen, and E. S. Saltzman
Atmos. Chem. Phys., 13, 11073–11087, https://doi.org/10.5194/acp-13-11073-2013, https://doi.org/10.5194/acp-13-11073-2013, 2013
Related subject area
Subject: Hydrosphere Interactions | Research Activity: Field Measurements | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Increasing and decreasing trends of the atmospheric deposition of organochlorine compounds in European remote areas during the last decade
Drivers of diel and regional variations of halocarbon emissions from the tropical North East Atlantic
Global sea-to-air flux climatology for bromoform, dibromomethane and methyl iodide
Organics in environmental ices: sources, chemistry, and impacts
Impact of biomass burning on ocean water quality in Southeast Asia through atmospheric deposition: field observations
L. Arellano, P. Fernández, R. Fonts, N. L. Rose, U. Nickus, H. Thies, E. Stuchlík, L. Camarero, J. Catalan, and J. O. Grimalt
Atmos. Chem. Phys., 15, 6069–6085, https://doi.org/10.5194/acp-15-6069-2015, https://doi.org/10.5194/acp-15-6069-2015, 2015
Short summary
Short summary
Despite the regulations in the use of polychlorobiphenyls (PCBs), an increase in atmospheric deposition fluxes of these pollutants in high-altitude mountain areas of Europe is observed for the period between 1996 and 2006. In contrast, atmospheric deposition of organochlorine pesticides showed a strong decrease. Volatilization from soils or melting glaciers related to climate change and the differences in physical–chemical properties between compounds may explain the observed temporal trend.
H. Hepach, B. Quack, F. Ziska, S. Fuhlbrügge, E. L. Atlas, K. Krüger, I. Peeken, and D. W. R. Wallace
Atmos. Chem. Phys., 14, 1255–1275, https://doi.org/10.5194/acp-14-1255-2014, https://doi.org/10.5194/acp-14-1255-2014, 2014
F. Ziska, B. Quack, K. Abrahamsson, S. D. Archer, E. Atlas, T. Bell, J. H. Butler, L. J. Carpenter, C. E. Jones, N. R. P. Harris, H. Hepach, K. G. Heumann, C. Hughes, J. Kuss, K. Krüger, P. Liss, R. M. Moore, A. Orlikowska, S. Raimund, C. E. Reeves, W. Reifenhäuser, A. D. Robinson, C. Schall, T. Tanhua, S. Tegtmeier, S. Turner, L. Wang, D. Wallace, J. Williams, H. Yamamoto, S. Yvon-Lewis, and Y. Yokouchi
Atmos. Chem. Phys., 13, 8915–8934, https://doi.org/10.5194/acp-13-8915-2013, https://doi.org/10.5194/acp-13-8915-2013, 2013
V. F. McNeill, A. M. Grannas, J. P. D. Abbatt, M. Ammann, P. Ariya, T. Bartels-Rausch, F. Domine, D. J. Donaldson, M. I. Guzman, D. Heger, T. F. Kahan, P. Klán, S. Masclin, C. Toubin, and D. Voisin
Atmos. Chem. Phys., 12, 9653–9678, https://doi.org/10.5194/acp-12-9653-2012, https://doi.org/10.5194/acp-12-9653-2012, 2012
P. Sundarambal, R. Balasubramanian, P. Tkalich, and J. He
Atmos. Chem. Phys., 10, 11323–11336, https://doi.org/10.5194/acp-10-11323-2010, https://doi.org/10.5194/acp-10-11323-2010, 2010
Cited articles
Alcolombri, U., Ben-Dor, S., Feldmesser, E., Levin, Y., Tawfik, D. S., and
Vardi, A.: Identification of the algal dimethyl sulfide–releasing enzyme: A
missing link in the marine sulfur cycle, Science, 348, 1466–1469,
https://doi.org/10.1126/science.aab1586, 2015.
Atkinson, R.: Kinetics and mechanisms of the gas-phase reactions of the
hydroxyl radical with organic compounds under atmospheric conditions, Chem.
Rev., 86, 69–201, https://doi.org/10.1021/cr00071a004, 1986.
Atkinson, R., Baulch, D. L., Cox, R. A., Hampson, R. F., Kerr, J. A., Rossi,
M. J., and Troe, J.: Evaluated Kinetic, Photochemical and Heterogeneous Data
for Atmospheric Chemistry: Supplement V. – IUPAC Subcommittee on Gas Kinetic
Data Evaluation for Atmospheric Chemistry, J. Phys. Chem. Ref. Data, 26, 521–1011, https://doi.org/10.1063/1.556011, 1997.
Ayers, G. P. and Gillett, R. W.: DMS and its oxidation products in the
remote marine atmosphere: implications for climate and atmospheric
chemistry, J. Sea Res., 43, 275–286, 2000.
Bandy, A. R., Thornton, D. C., Blomquist, B. W., Chen, S., Wade, T. P.,
Ianni, J. C., Mitchell, G. M., and Nadler, W.: Chemistry of dimethyl sulfide
in the equatorial Pacific atmosphere, Geophys. Res. Lett., 23,
741–744, https://doi.org/10.1029/96gl00779, 1996.
Beale, R., Dixon, J. L., Arnold, S. R., Liss, P. S., and Nightingale, P. D.:
Methanol, acetaldehyde, and acetone in the surface waters of the Atlantic
Ocean, J. Geophys. Res.-Oceans, 118, 5412–5425,
https://doi.org/10.1002/jgrc.20322, 2013.
Beale, R., Dixon, J. L., Smyth, T. J., and Nightingale, P. D.: Annual study
of oxygenated volatile organic compounds in UK shelf waters, Mar. Chem.,
171, 96–106, https://doi.org/10.1016/j.marchem.2015.02.013, 2015.
Bell, T. G., De Bruyn, W., Miller, S. D., Ward, B., Christensen, K. H., and Saltzman, E. S.: Air–sea dimethylsulfide (DMS) gas transfer in the North Atlantic: evidence for limited interfacial gas exchange at high wind speed, Atmos. Chem. Phys., 13, 11073–11087, https://doi.org/10.5194/acp-13-11073-2013, 2013.
Bell, T. G., De Bruyn, W., Marandino, C. A., Miller, S. D., Law, C. S., Smith, M. J., and Saltzman, E. S.: Dimethylsulfide gas transfer coefficients from algal blooms in the Southern Ocean, Atmos. Chem. Phys., 15, 1783–1794, https://doi.org/10.5194/acp-15-1783-2015, 2015.
Berresheim, H.: Biogenic sulfur emissions from the Subantarctic and
Antarctic Oceans, J. Geophys. Res., 92, 13245–13262,
https://doi.org/10.1029/JD092iD11p13245, 1987.
Burrell, T. J.: Bacterial extracellular enzyme activity in a future ocean,
PhD thesis, Victoria University of Wellington, 324 pp., 2015.
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.
Carpenter, L. J. and Nightingale, P. D.: Chemistry and Release of Gases
from the Surface Ocean, Chem. Rev., 115, 4015–4034, https://doi.org/10.1021/cr5007123,
2015.
Charlson, R., Lovelock, J., Andreae, M., and Warren, S.: Oceanic
phytoplankton, atmospheric sulphur, cloud albedo and climate, Nature, 326, 655–661, https://doi.org/10.1038/326655a0, 1987.
Colomb, A., Gros, V., Alvain, S., Sarda-Esteve, R., Bonsang, B., Moulin, C.,
Klupfel, T., and Williams, J.: Variation of atmospheric volatile organic
compounds over the Southern Indian Ocean (30-49∘ S),
Environ. Chem., 6, 70–82, https://doi.org/10.1071/en08072, 2009.
de Bruyn, W. J., Clark, C. D., Pagel, L., and Takehara, C.: Photochemical
production of formaldehyde, acetaldehyde and acetone from chromophoric
dissolved organic matter in coastal waters, J. Photoch. Photobio. A, 226, 16–22, https://doi.org/10.1016/j.jphotochem.2011.10.002,
2012.
Dixon, J. L., Beale, R., and Nightingale, P. D.: Production of methanol,
acetaldehyde, and acetone in the Atlantic Ocean, Geophys. Res. Lett., 40, 4700–4705, https://doi.org/10.1002/grl.50922, 2013.
Feilberg, A., Liu, D., Adamsen, A. P. S., Hansen, M. J., and Jonassen, K. E.
N.: Odorant Emissions from Intensive Pig Production Measured by Online
Proton-Transfer-Reaction Mass Spectrometry, Environ. Sci.
Technol., 44, 5894–5900, https://doi.org/10.1021/es100483s, 2010.
Fischer, E. V., Jacob, D. J., Millet, D. B., Yantosca, R. M., and Mao, J.:
The role of the ocean in the global atmospheric budget of acetone,
Geophys. Res. Lett., 39, L01807, https://doi.org/10.1029/2011gl050086, 2012.
Flöck, O. R. and Andreae, M. O.: Photochemical and non-photochemical
formation and destruction of carbonyl sulfide and methyl mercaptan in ocean
waters, Mar. Chem., 54, 11–26,
https://doi.org/10.1016/0304-4203(96)00027-8, 1996.
Galbally, I. E., Lawson, S. J., Weeks, I. A., Bentley, S. T., Gillett, R.
W., Meyer, M., and Goldstein, A. H.: Volatile organic compounds in marine
air at Cape Grim, Australia, Environ. Chem., 4, 178–182,
https://doi.org/10.1071/en07024, 2007.
Gall, M. P., Davies-Colley, R. J., and Merrilees, R. A.: Exceptional visual
clarity and optical purity in a sub-alpine lake, Limnol. Oceanogr.,
58, 443–451, https://doi.org/10.4319/lo.2013.58.2.0443, 2013.
Hall, J. A. and Safi, K.: The impact of in situ Fe fertilisation on the
microbial food web in the Southern Ocean, Deep-Sea Res. Pt II, 48, 2591–2613,
https://doi.org/10.1016/S0967-0645(01)00010-8, 2001.
Halsey, K. H., Giovannoni, S. J., Graus, M., Zhao, Y., Landry, Z., Thrash,
J. C., Vergin, K. L., and de Gouw, J.: Biological cycling of volatile
organic carbon by phytoplankton and bacterioplankton, Limnol.
Oceanogr., 62, 2650–2661, https://doi.org/10.1002/lno.10596, 2017.
ISO: ISO 6879: Air Quality, Performance Characteristics and Related Concepts
for Air Quality Measuring Methods, International Organisation for
Standardisation, Geneva, Switzerland, 1995.
Jacob, D. J., Field, B. D., Jin, E. M., Bey, I., Li, Q. B., Logan, J. A.,
Yantosca, R. M., and Singh, H. B.: Atmospheric budget of acetone, J.
Geophys. Res.-Atmos., 107, 4100, https://doi.org/10.1029/2001jd000694, 2002.
Johnson, M. T.: A numerical scheme to calculate temperature and salinity dependent air-water transfer velocities for any gas, Ocean Sci., 6, 913–932, https://doi.org/10.5194/os-6-913-2010, 2010.
Jones, A. R., Thomson, D. J., Hort, M., and Devenish, B.: The UK Met
Office's next-generation atmospheric dispersion model, NAME III, in:
Proceedings of the 27th NATO/CCMS International Technical Meeting on Air
Pollution Modelling and its Application, edited by: Borrego, C. and Norman,
A.-L., Springer, 580–589, 2007.
Kettle, A. J., Rhee, T. S., von Hobe, M., Poulton, A., Aiken, J., and
Andreae, M. O.: Assessing the flux of different volatile sulfur gases from
the ocean to the atmosphere, J. Geophys. Res., 106,
12193–12209, https://doi.org/10.1029/2000jd900630, 2001.
Kieber, R. J., Zhou, X., and Mopper, K.: Formation of carbonyl compounds
from UV-induced photodegradation of humic substances in natural waters: Fate
of riverine carbon in the sea, Limnol. Oceanogr., 35, 1503–1515,
https://doi.org/10.4319/lo.1990.35.7.1503, 1990.
Kiene, R. P.: Production of methanethiol from dimethylsulfoniopropionate in
marine surface waters, Mar. Chem., 54, 69–83,
https://doi.org/10.1016/0304-4203(96)00006-0, 1996.
Kiene, R. P. and Linn, L. J.: The fate of dissolved
dimethylsulfoniopropionate (DMSP) in seawater: tracer studies using
35S-DMSP, Geochim. Cosmochim. Ac., 64, 2797–2810,
https://doi.org/10.1016/S0016-7037(00)00399-9, 2000.
Kiene, R. P., Linn, L. J., and Bruton, J. A.: New and important roles for
DMSP in marine microbial communities, J. Sea Res., 43, 209–224,
https://doi.org/10.1016/S1385-1101(00)00023-X, 2000.
Kiene, R. P., Williams, T. E., Esson, K., Tortell, P. D., and Dacey, J. W.
H.: Methanethiol Concentrations and Sea-Air Fluxes in the Subarctic NE
Pacific Ocean, American Geophysical Union, Fall meeting, 2017.
Kwan, A. J., Crounse, J. D., Clarke, A. D., Shinozuka, Y., Anderson, B. E.,
Crawford, J. H., Avery, M. A., McNaughton, C. S., Brune, W. H., Singh, H.
B., and Wennberg, P. O.: On the flux of oxygenated volatile organic
compounds from organic aerosol oxidation, Geophys. Res. Lett., 33, L15815,
https://doi.org/10.1029/2006gl026144, 2006.
Lana, A., Bell, T. G., Simó, 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.
Law, C. S., Brévière, E., de Leeuw, G., Garçon, V., Guieu, C.,
Kieber, D. J., Kontradowitz, S., Paulmier, A., Quinn, P. K., Saltzman, E.
S., Stefels, J., and von Glasow, R.: Evolving research directions in Surface
Ocean–Lower Atmosphere (SOLAS) science, Environ. Chem., 10, 1–16,
https://doi.org/10.1071/EN12159, 2013.
Law, C. S., Smith, M. J., Harvey, M. J., Bell, T. G., Cravigan, L. T., Elliott, F. C., Lawson, S. J., Lizotte, M., Marriner, A., McGregor, J., Ristovski, Z., Safi, K. A., Saltzman, E. S., Vaattovaara, P., and Walker, C. F.: Overview and preliminary results of the Surface Ocean Aerosol Production (SOAP) campaign, Atmos. Chem. Phys., 17, 13645–13667, https://doi.org/10.5194/acp-17-13645-2017, 2017.
Law, C. S., Woodward, E. M. S., Ellwood, M. J., Marriner, A., Bury, S. J.,
and Safi, K. A.: Response of surface nutrient inventories and nitrogen
fixation to a tropical cyclone in the southwest Pacific, Limnol. Oceanogr.,
56, 1372–1385, https://doi.org/10.4319/lo.2011.56.4.1372, 2011.
Lawson, S.: DMS, acetone, methanethiol atmospheric data from SOAP voyage. v1. CSIRO, Data Collection, https://doi.org/10.25919/5d914b00c5759, 2019.
Lawson, S. J., Selleck, P. W., Galbally, I. E., Keywood, M. D., Harvey, M. J., Lerot, C., Helmig, D., and Ristovski, Z.: Seasonal in situ observations of glyoxal and methylglyoxal over the temperate oceans of the Southern Hemisphere, Atmos. Chem. Phys., 15, 223–240, https://doi.org/10.5194/acp-15-223-2015, 2015.
Leck, C. and Rodhe, H..: Emissions of marine biogenic sulfur to the
atmosphere of northern Europe, J. Atmos. Chem., 12, 63–86,
https://doi.org/10.1007/bf00053934, 1991.
Lee, C. L. and Brimblecombe, P.: Anthropogenic contributions to global
carbonyl sulfide, carbon disulfide and organosulfides fluxes, Earth-Sci.
Rev., 160, 1–18, https://doi.org/10.1016/j.earscirev.2016.06.005, 2016.
Lewis, A. C., Hopkins, J. R., Carpenter, L. J., Stanton, J., Read, K. A., and Pilling, M. J.: Sources and sinks of acetone, methanol, and acetaldehyde in North Atlantic marine air, Atmos. Chem. Phys., 5, 1963–1974, https://doi.org/10.5194/acp-5-1963-2005, 2005.
Liss, P. S. and Johnson, M. T. (Eds.): Ocean-Atmosphere Interactions of Gases and Particles, Springer Earth System
Sciences, 315 pp., 2014.
Lizotte, M., Levasseur, M., Law, C. S., Walker, C. F., Safi, K. A., Marriner, A., and Kiene, R. P.: Dimethylsulfoniopropionate (DMSP) and dimethyl sulfide (DMS) cycling across contrasting biological hotspots of the New Zealand subtropical front, Ocean Sci., 13, 961–982, https://doi.org/10.5194/os-13-961-2017, 2017.
Malin, G.: Sulphur, climate and the microbial maze, Nature, 387, 857–858,
https://doi.org/10.1038/43075, 1997.
Marandino, C. A., De Bruyn, W. J., Miller, S. D., Prather, M. J., and
Saltzman, E. S.: Oceanic uptake and the global atmospheric acetone budget,
Geophys. Res. Lett., 32, L15806, https://doi.org/10.1029/2005gl023285, 2005.
Marandino, C. A., De Bruyn, W. J., Miller, S. D., and Saltzman, E. S.: Eddy
correlation measurements of the air/sea flux of dimethylsulfide over the
North Pacific Ocean, J. Geophys. Res.-Atmos., 112, D03301,
https://doi.org/10.1029/2006jd007293, 2007.
Nemecek-Marshall, M., Wojciechowski, C., Kuzma, J., Silver, G. M., and Fall,
R.: Marine Vibrio species produce the volatile organic compound acetone,
Appl. Environ. Microbiol., 61, 44–47, 1995.
Nemecek-Marshall, M., Wojciechowski, C., Wagner, W. P., and Fall, R.:
Acetone formation in the Vibrio family: a new pathway for bacterial leucine
catabolism, J. Bacteriol., 181, 7493–7499, 1999.
Nodder, S. D., Chiswell, S. M., and Northcote, L. C.: Annual cycles of
deep-ocean biogeochemical export fluxes in subtropical and subantarctic
waters, southwest Pacific Ocean, J. Geophys. Res.-Oceans,
121, 2405–2424, https://doi.org/10.1002/2015jc011243, 2016.
Pan, X., Underwood, J. S., Xing, J.-H., Mang, S. A., and Nizkorodov, S. A.: Photodegradation of secondary organic aerosol generated from limonene oxidation by ozone studied with chemical ionization mass spectrometry, Atmos. Chem. Phys., 9, 3851–3865, https://doi.org/10.5194/acp-9-3851-2009, 2009.
Quinn, P. K. and Bates, T. S.: The case against climate regulation via
oceanic phytoplankton sulphur emissions, Nature, 480, 51–56,
https://doi.org/10.1038/nature10580, 2011.
Read, K. A., Carpenter, L. J., Arnold, S. R., Beale, R., Nightingale, P. D.,
Hopkins, J. R., Lewis, A. C., Lee, J. D., Mendes, L., and Pickering, S. J.:
Multiannual Observations of Acetone, Methanol, and Acetaldehyde in Remote
Tropical Atlantic Air: Implications for Atmospheric OVOC Budgets and
Oxidative Capacity, Environ. Sci. Technol., 46, 11028–11039,
https://doi.org/10.1021/es302082p, 2012.
Safi, K. A., Griffiths, F. B., and Hall, J. A.: Microzooplankton composition,
biomass and grazing rates along the WOCE SR3 line between Tasmania and
Antarctica, Deep-Sea Res. Pt I, 54,
1025–1041, https://doi.org/10.1016/j.dsr.2007.05.003, 2007.
Sander, R.: Compilation of Henry's law constants (version 4.0) for water as solvent, Atmos. Chem. Phys., 15, 4399–4981, https://doi.org/10.5194/acp-15-4399-2015, 2015.
Schlundt, C., Tegtmeier, S., Lennartz, S. T., Bracher, A., Cheah, W., Krüger, K., Quack, B., and Marandino, C. A.: Oxygenated volatile organic carbon in the western Pacific convective center: ocean cycling, air–sea gas exchange and atmospheric transport, Atmos. Chem. Phys., 17, 10837–10854, https://doi.org/10.5194/acp-17-10837-2017, 2017.
Simó, R. and Pedrós-Alió, C.: Short-term variability in the
open ocean cycle of dimethylsulfide, Glocal Biogeochem. Cy., 13,
1173–1181, https://doi.org/10.1029/1999gb900081, 1999.
Sinha, V., Williams, J., Meyerhöfer, M., Riebesell, U., Paulino, A. I., and Larsen, A.: Air-sea fluxes of methanol, acetone, acetaldehyde, isoprene and DMS from a Norwegian fjord following a phytoplankton bloom in a mesocosm experiment, Atmos. Chem. Phys., 7, 739–755, https://doi.org/10.5194/acp-7-739-2007, 2007.
Smith, M. J., Walker, C. F., Bell, T. G., Harvey, M. J., Saltzman, E. S., and Law, C. S.: Gradient flux measurements of sea–air DMS transfer during the Surface Ocean Aerosol Production (SOAP) experiment, Atmos. Chem. Phys., 18, 5861–5877, https://doi.org/10.5194/acp-18-5861-2018, 2018.
Somogyi, M.: Notes on Sugar Determination, J. Biol. Chem.,
70, 599–612, 1926.
Somogyi, M.: Notes on Sugar Determination, J. Biol. Chem.,
195, 19–23, 1952.
Sun, J., Todd, J. D., Thrash, J. C., Qian, Y., Qian, M. C., Temperton, B.,
Guo, J., Fowler, E. K., Aldrich, J. T., Nicora, C. D., Lipton, M. S., Smith,
R. D., De Leenheer, P., Payne, S. H., Johnston, A. W. B., Davie-Martin, C.
L., Halsey, K. H., and Giovannoni, S. J.: The abundant marine bacterium
Pelagibacter simultaneously catabolizes dimethylsulfoniopropionate to the
gases dimethyl sulfide and methanethiol, Nat. Microbiol., 1, 16065,
https://doi.org/10.1038/nmicrobiol.2016.65,
2016.
Taddei, S., Toscano, P., Gioli, B., Matese, A., Miglietta, F., Vaccari, F.
P., Zaldei, A., Custer, T., and Williams, J.: Carbon Dioxide and Acetone
Air−Sea Fluxes over the Southern Atlantic, Environ. Sci.
Technol., 43, 5218-5222, https://doi.org/10.1021/es8032617, 2009.
Tanimoto, H., Kameyama, S., Iwata, T., Inomata, S., and Omori, Y.:
Measurement of Air-Sea Exchange of Dimethyl Sulfide and Acetone by PTR-MS
Coupled with Gradient Flux Technique, Environ. Sci. Technol.,
48, 526–533, https://doi.org/10.1021/es4032562, 2014.
Tyndall, G. S. and Ravishankara, A. R.: Atmospheric oxidation of reduced
sulfur species, Int. J. Chem. Kinet., 23, 483–527,
https://doi.org/10.1002/kin.550230604, 1991.
Walker, C. F., Harvey, M. J., Smith, M. J., Bell, T. G., Saltzman, E. S., Marriner, A. S., McGregor, J. A., and Law, C. S.: Assessing the potential for dimethylsulfide enrichment at the sea surface and its influence on air–sea flux, Ocean Sci., 12, 1033–1048, https://doi.org/10.5194/os-12-1033-2016, 2016.
Warneke, C. and de Gouw, J. A.: Organic trace gas composition of the marine
boundary layer over the northwest Indian Ocean in April 2000, Atmos.
Environ., 35, 5923–5933, 2001.
Williams, T. L., Adams, N. G., and Babcock, L. M.: Selected ion flow tube
studies of H3O+(H2O)0.1 reactions with sulfides and
thiols, Int. J. Mass Spectrom., 172,
149–159, https://doi.org/10.1016/S0168-1176(97)00081-5, 1998.
Williams, J., Holzinger, R., Gros, V., Xu, X., Atlas, E., and Wallace, D. W.
R.: Measurements of organic species in air and seawater from the tropical
Atlantic, Geophys. Res. Lett., 31, L23S06, https://doi.org/10.1029/2004gl020012, 2004.
Williams, J., Custer, T., Riede, H., Sander, R., Jöckel, P., Hoor, P.,
Pozzer, A., Wong-Zehnpfennig, S., Hosaynali Beygi, Z., Fischer, H., Gros,
V., Colomb, A., Bonsang, B., Yassaa, N., Peeken, I., Atlas, E. L., Waluda,
C. M., van Aardenne, J. A., and Lelieveld, J.: Assessing the effect of
marine isoprene and ship emissions on ozone, using modelling and
measurements from the South Atlantic Ocean, Environ. Chem., 7,
171–182, https://doi.org/10.1071/EN09154, 2010.
Yang, M., Beale, R., Liss, P., Johnson, M., Blomquist, B., and Nightingale, P.: Air–sea fluxes of oxygenated volatile organic compounds across the Atlantic Ocean, Atmos. Chem. Phys., 14, 7499–7517, https://doi.org/10.5194/acp-14-7499-2014, 2014a.
Yang, M., Blomquist, B. W., and Nightingale, P. D.: Air-sea exchange of
methanol and acetone during HiWinGS: Estimation of air phase, water phase
gas transfer velocities, J. Geophys. Res.-Oceans, 119, 7308–7323, https://doi.org/10.1002/2014jc010227, 2014b.
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.
Yvon, S. A., Cooper, D. J., Koropalov, V., and Saltzman, E. S.: Atmospheric
hydrogen sulfide over the equatorial Pacific (SAGA 3), J.
Geophys. Res.-Atmos., 98, 16979–16983, https://doi.org/10.1029/92jd00451, 1993.
Zhou, X. and Mopper, K.: Photochemical production of low-molecular-weight
carbonyl compounds in seawater and surface microlayer and their air-sea
exchange, Mar. Chem., 56, 201–213,
https://doi.org/10.1016/S0304-4203(96)00076-X, 1997.
Short summary
Methanethiol (MeSH) is a reduced sulfur gas originating from phytoplankton, with a global ocean source of ~ 17 % of dimethyl sulfide (DMS). It has been little studied and is rarely observed over the ocean. In this work, MeSH was measured at much higher levels than previously observed (3–36 % of parallel DMS mixing ratios). MeSH could be a significant source of atmospheric sulfur over productive regions of the ocean, but its distribution, and its atmospheric impact, requires more investigation.
Methanethiol (MeSH) is a reduced sulfur gas originating from phytoplankton, with a global ocean...
Altmetrics
Final-revised paper
Preprint