Articles | Volume 17, issue 22
https://doi.org/10.5194/acp-17-13645-2017
© Author(s) 2017. 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-17-13645-2017
© Author(s) 2017. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Research article
| 
16 Nov 2017
Research article |
| 16 Nov 2017
| 16 Nov 2017
Overview and preliminary results of the Surface Ocean Aerosol Production (SOAP) campaign
National Institute of Water and Atmospheric Research, Wellington, New
Zealand
Department of Chemistry, University of Otago, Dunedin, New Zealand
Murray J. Smith
National Institute of Water and Atmospheric Research, Wellington, New
Zealand
Mike J. Harvey
National Institute of Water and Atmospheric Research, Wellington, New
Zealand
Thomas G. Bell
Plymouth Marine Laboratory, Prospect Place, The Hoe, Plymouth, UK
Department of Earth System Science, University of California,
Irvine, CA, USA
Luke T. Cravigan
Climate Science Centre, Commonwealth Scientific and Industrial
Research Organisation, Aspendale, Australia
International Laboratory for Air Quality and Health, Queensland
University of Technology, Brisbane, Australia
Fiona C. Elliott
National Institute of Water and Atmospheric Research, Wellington, New
Zealand
Sarah J. Lawson
Commonwealth Scientific and Industrial Research Organisation,
Oceans and Atmosphere Flagship, Aspendale, Australia
Martine Lizotte
Department of Biology (Québec-Océan), Université Laval, Québec City, Québec, Canada
Andrew Marriner
National Institute of Water and Atmospheric Research, Wellington, New
Zealand
John McGregor
National Institute of Water and Atmospheric Research, Wellington, New
Zealand
Zoran Ristovski
International Laboratory for Air Quality and Health, Queensland
University of Technology, Brisbane, Australia
Karl A. Safi
National Institute of Water and Atmospheric Research, Hamilton, New
Zealand
Eric S. Saltzman
Department of Earth System Science, University of California,
Irvine, CA, USA
Petri Vaattovaara
University of Eastern Finland, Kuopio, Finland
Carolyn F. Walker
National Institute of Water and Atmospheric Research, Wellington, New
Zealand
Related authors
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.
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.
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.
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.
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.
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.
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.
Sarah J. Lawson, Cliff S. Law, Mike J. Harvey, Thomas G. Bell, Carolyn F. Walker, Warren J. de Bruyn, and Eric S. Saltzman
Atmos. Chem. Phys., 20, 3061–3078, https://doi.org/10.5194/acp-20-3061-2020, https://doi.org/10.5194/acp-20-3061-2020, 2020
Short summary
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.
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.
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.
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.
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.
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
E. Johanna Horchler, Joel Alroe, Luke Harrison, Luke Cravigan, Daniel P. Harrison, and Zoran D. Ristovski
EGUsphere, https://doi.org/10.5194/egusphere-2025-465, https://doi.org/10.5194/egusphere-2025-465, 2025
Short summary
Short summary
Aerosols play a role in global climate by interacting with incoming solar radiation and by taking up water vapour from the atmosphere to form clouds. Enhancing local-scale cloud cover can reduce sea surface temperatures. Coral bleaching events increased in the Great Barrier Reef (GBR) as sea surface temperatures rise. Our study found that the number of aerosols and the cloud forming ability over the GBR increased if the aerosols were transported from inland Australia rather than the ocean.
Behnaz Alinaghipour, Sadegh Niazi, Robert Groth, Branka Miljevic, and Zoran Ristovski
Atmos. Meas. Tech., 18, 1063–1071, https://doi.org/10.5194/amt-18-1063-2025, https://doi.org/10.5194/amt-18-1063-2025, 2025
Short summary
Short summary
Airborne particles are crucial in environmental and health studies, requiring precise sampling for accurate characterisation. Our study examines the optimal sampling time for the TSI Nanometer Aerosol Sampler 3089 at different input concentrations. Aerosols from low-, medium-, and high-concentration environments were sampled over 1, 3, and 6 h. A linear relationship was observed using a regression model between the deposition densities and the product of input concentration and sampling time.
Alex T. Archibald, Bablu Sinha, Maria R. Russo, Emily Matthews, Freya A. Squires, N. Luke Abraham, Stephane J.-B. Bauguitte, Thomas J. Bannan, Thomas G. Bell, David Berry, Lucy J. Carpenter, Hugh Coe, Andrew Coward, Peter Edwards, Daniel Feltham, Dwayne Heard, Jim Hopkins, James Keeble, Elizabeth C. Kent, Brian A. King, Isobel R. Lawrence, James Lee, Claire R. Macintosh, Alex Megann, Bengamin I. Moat, Katie Read, Chris Reed, Malcolm J. Roberts, Reinhard Schiemann, David Schroeder, Timothy J. Smyth, Loren Temple, Navaneeth Thamban, Lisa Whalley, Simon Williams, Huihui Wu, and Mingxi Yang
Earth Syst. Sci. Data, 17, 135–164, https://doi.org/10.5194/essd-17-135-2025, https://doi.org/10.5194/essd-17-135-2025, 2025
Short summary
Short summary
Here, we present an overview of the data generated as part of the North Atlantic Climate System Integrated Study (ACSIS) programme that 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). The datasets described here cover the North Atlantic Ocean, the atmosphere above (it including its composition), and Arctic sea ice.
Yik-Sze Lau, Zoran Ristovski, and Branka Miljevic
Atmos. Meas. Tech. Discuss., https://doi.org/10.5194/amt-2024-192, https://doi.org/10.5194/amt-2024-192, 2025
Revised manuscript accepted for AMT
Short summary
Short summary
The chemical properties of aerosols in the atmosphere significantly influence their impact on global climate and human health. The current study constructed an instrumental system (HEAC/ESI-Orbitrap-MS) for the real-time chemical analysis of aerosol samples. The combined system successfully identified over three hundred chemical compounds in aerosol samples in real-time, showing the robustness of the technique for the chemical characterisation of aerosols under atmospheric relevant 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.
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.
Martine Lizotte, Bennet Juhls, Atsushi Matsuoka, Philippe Massicotte, Gaëlle Mével, David Obie James Anikina, Sofia Antonova, Guislain Bécu, Marine Béguin, Simon Bélanger, Thomas Bossé-Demers, Lisa Bröder, Flavienne Bruyant, Gwénaëlle Chaillou, Jérôme Comte, Raoul-Marie Couture, Emmanuel Devred, Gabrièle Deslongchamps, Thibaud Dezutter, Miles Dillon, David Doxaran, Aude Flamand, Frank Fell, Joannie Ferland, Marie-Hélène Forget, Michael Fritz, Thomas J. Gordon, Caroline Guilmette, Andrea Hilborn, Rachel Hussherr, Charlotte Irish, Fabien Joux, Lauren Kipp, Audrey Laberge-Carignan, Hugues Lantuit, Edouard Leymarie, Antonio Mannino, Juliette Maury, Paul Overduin, Laurent Oziel, Colin Stedmon, Crystal Thomas, Lucas Tisserand, Jean-Éric Tremblay, Jorien Vonk, Dustin Whalen, and Marcel Babin
Earth Syst. Sci. Data, 15, 1617–1653, https://doi.org/10.5194/essd-15-1617-2023, https://doi.org/10.5194/essd-15-1617-2023, 2023
Short summary
Short summary
Permafrost thaw in the Mackenzie Delta region results in the release of organic matter into the coastal marine environment. What happens to this carbon-rich organic matter as it transits along the fresh to salty aquatic environments is still underdocumented. Four expeditions were conducted from April to September 2019 in the coastal area of the Beaufort Sea to study the fate of organic matter. This paper describes a rich set of data characterizing the composition and sources of organic matter.
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.
Ruhi S. Humphries, Melita D. Keywood, Jason P. Ward, James Harnwell, Simon P. Alexander, Andrew R. Klekociuk, Keiichiro Hara, Ian M. McRobert, Alain Protat, Joel Alroe, Luke T. Cravigan, Branka Miljevic, Zoran D. Ristovski, Robyn Schofield, Stephen R. Wilson, Connor J. Flynn, Gourihar R. Kulkarni, Gerald G. Mace, Greg M. McFarquhar, Scott D. Chambers, Alastair G. Williams, and Alan D. Griffiths
Atmos. Chem. Phys., 23, 3749–3777, https://doi.org/10.5194/acp-23-3749-2023, https://doi.org/10.5194/acp-23-3749-2023, 2023
Short summary
Short summary
Observations of aerosols in pristine regions are rare but are vital to constraining the natural baseline from which climate simulations are calculated. Here we present recent seasonal observations of aerosols from the Southern Ocean and contrast them with measurements from Antarctica, Australia and regionally relevant voyages. Strong seasonal cycles persist, but striking differences occur at different latitudes. This study highlights the need for more long-term observations in remote regions.
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.
Peter Sperlich, Gordon W. Brailsford, Rowena C. Moss, John McGregor, Ross J. Martin, Sylvia Nichol, Sara Mikaloff-Fletcher, Beata Bukosa, Magda Mandic, C. Ian Schipper, Paul Krummel, and Alan D. Griffiths
Atmos. Meas. Tech., 15, 1631–1656, https://doi.org/10.5194/amt-15-1631-2022, https://doi.org/10.5194/amt-15-1631-2022, 2022
Short summary
Short summary
We tested an in situ analyser for carbon and oxygen isotopes in atmospheric CO2 at Baring Head, New Zealand’s observatory for Southern Ocean baseline air. The analyser was able to resolve regional signals of the terrestrial carbon cycle, although the analysis of small events was limited by analytical uncertainty. Further improvement of the instrument performance would be desirable for the robust analysis of distant signals and to resolve the small variability in Southern Ocean baseline air.
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.
Sonya L. Fiddes, Matthew T. Woodhouse, Steve Utembe, Robyn Schofield, Simon P. Alexander, Joel Alroe, Scott D. Chambers, Zhenyi Chen, Luke Cravigan, Erin Dunne, Ruhi S. Humphries, Graham Johnson, Melita D. Keywood, Todd P. Lane, Branka Miljevic, Yuko Omori, Alain Protat, Zoran Ristovski, Paul Selleck, Hilton B. Swan, Hiroshi Tanimoto, Jason P. Ward, and Alastair G. Williams
Atmos. Chem. Phys., 22, 2419–2445, https://doi.org/10.5194/acp-22-2419-2022, https://doi.org/10.5194/acp-22-2419-2022, 2022
Short summary
Short summary
Coral reefs have been found to produce the climatically relevant chemical compound dimethyl sulfide (DMS). It has been suggested that corals can modify their environment via the production of DMS. We use an atmospheric chemistry model to test this theory at a regional scale for the first time. We find that it is unlikely that coral-reef-derived DMS has an influence over local climate, in part due to the proximity to terrestrial and anthropogenic aerosol sources.
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.
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.
Joel Alroe, Luke T. Cravigan, Branka Miljevic, Graham R. Johnson, Paul Selleck, Ruhi S. Humphries, Melita D. Keywood, Scott D. Chambers, Alastair G. Williams, and Zoran D. Ristovski
Atmos. Chem. Phys., 20, 8047–8062, https://doi.org/10.5194/acp-20-8047-2020, https://doi.org/10.5194/acp-20-8047-2020, 2020
Short summary
Short summary
We present findings from an austral summer voyage across the full latitudinal width of the Southern Ocean, south of Australia. Aerosol properties were strongly influenced by marine biological activity, synoptic-scale weather systems, and long-range transport of continental-influenced air masses. The meteorological history of the sampled air masses is shown to have a vital limiting influence on cloud condensation nuclei and the accuracy of modelled sea spray aerosol concentrations.
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.
Mathieu Casado, Gwenaëlle Gremion, Paul Rosenbaum, Jilda Alicia Caccavo, Kelsey Aho, Nicolas Champollion, Sarah L. Connors, Adrian Dahood, Alfonso Fernandez, Martine Lizotte, Katja Mintenbeck, Elvira Poloczanska, and Gerlis Fugmann
Geosci. Commun., 3, 89–97, https://doi.org/10.5194/gc-3-89-2020, https://doi.org/10.5194/gc-3-89-2020, 2020
Short summary
Short summary
Early-career scientists (ECSs) are rarely invited to act as peer reviewers. Participating in a group peer review of the IPCC Special Report on Ocean and Cryosphere in a Changing Climate, PhD students spent more time reviewing than more established scientists and provided a similar proportion of substantive comments. By soliciting and including ECSs in peer review, the scientific community would reduce the burden on more established scientists and may improve the quality of that process.
Martine Lizotte, Maurice Levasseur, Virginie Galindo, Margaux Gourdal, Michel Gosselin, Jean-Éric Tremblay, Marjolaine Blais, Joannie Charette, and Rachel Hussherr
Biogeosciences, 17, 1557–1581, https://doi.org/10.5194/bg-17-1557-2020, https://doi.org/10.5194/bg-17-1557-2020, 2020
Short summary
Short summary
This study brings further support to the premise that the prevalence of younger and thinner icescapes over older and thicker ones in the Canadian High Arctic favors the early development of under-ice microorganisms as well as their production of the climate-relevant gas dimethylsulfide (DMS). Given the rapid rate of climate-driven changes in Arctic sea ice, our results suggest implications for the timing and magnitude of DMS pulses in the Arctic, with ramifications for climate forecasting.
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.
Sarah J. Lawson, Cliff S. Law, Mike J. Harvey, Thomas G. Bell, Carolyn F. Walker, Warren J. de Bruyn, and Eric S. Saltzman
Atmos. Chem. Phys., 20, 3061–3078, https://doi.org/10.5194/acp-20-3061-2020, https://doi.org/10.5194/acp-20-3061-2020, 2020
Short summary
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.
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.
Roya Ghahreman, Wanmin Gong, Martí Galí, Ann-Lise Norman, Stephen R. Beagley, Ayodeji Akingunola, Qiong Zheng, Alexandru Lupu, Martine Lizotte, Maurice Levasseur, and W. Richard Leaitch
Atmos. Chem. Phys., 19, 14455–14476, https://doi.org/10.5194/acp-19-14455-2019, https://doi.org/10.5194/acp-19-14455-2019, 2019
Short summary
Short summary
Atmospheric DMS(g) is a climatically important compound and the main source of biogenic sulfate in the Arctic. Its abundance in the Arctic increases during summer due to greater ice-free sea surface and higher biological activity. In this study, we implemented DMS(g) in a regional air quality forecast model configured for the Arctic. The study showed a significant impact from DMS(g) on sulfate aerosols, particularly in the 50–100 nm size range, in the Arctic marine boundary layer during summer.
Reece A. Brown, Svetlana Stevanovic, Steven Bottle, and Zoran D. Ristovski
Atmos. Meas. Tech., 12, 2387–2401, https://doi.org/10.5194/amt-12-2387-2019, https://doi.org/10.5194/amt-12-2387-2019, 2019
Short summary
Short summary
The paper details the design and characterization of a novel instrument for the measurement of particle reactivity and potential bioactivity, the PINQ. It continuously collects particles, regardless of size or composition, directly into a very small amount of liquid with a collection efficiency of > 0.97 and a cut-off size of 20 nm. PINQ has the highest time resolution, of only 1 min, and is very sensitive to various reactive species from the air.
Robin Bénard, Maurice Levasseur, Michael Scarratt, Sonia Michaud, Michel Starr, Alfonso Mucci, Gustavo Ferreyra, Michel Gosselin, Jean-Éric Tremblay, Martine Lizotte, and Gui-Peng Yang
Biogeosciences, 16, 1167–1185, https://doi.org/10.5194/bg-16-1167-2019, https://doi.org/10.5194/bg-16-1167-2019, 2019
Short summary
Short summary
We present rare data on the combined effects of acidification and warming on dimethylsulfide (DMS) during a mesocosm experiment. Our results show a reduction of DMS under elevated pCO2, but warming the mesocosms by 5 °C translated into a positive offset in concentrations of DMS over the whole range of pCO2 tested. Our results suggest that warming could mitigate the expected reduction in DMS production due to OA, even increasing the net DMS production, with possible repercussions for the climate.
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.
Jonathan P. D. Abbatt, W. Richard Leaitch, Amir A. Aliabadi, Allan K. Bertram, Jean-Pierre Blanchet, Aude Boivin-Rioux, Heiko Bozem, Julia Burkart, Rachel Y. W. Chang, Joannie Charette, Jai P. Chaubey, Robert J. Christensen, Ana Cirisan, Douglas B. Collins, Betty Croft, Joelle Dionne, Greg J. Evans, Christopher G. Fletcher, Martí Galí, Roya Ghahreman, Eric Girard, Wanmin Gong, Michel Gosselin, Margaux Gourdal, Sarah J. Hanna, Hakase Hayashida, Andreas B. Herber, Sareh Hesaraki, Peter Hoor, Lin Huang, Rachel Hussherr, Victoria E. Irish, Setigui A. Keita, John K. Kodros, Franziska Köllner, Felicia Kolonjari, Daniel Kunkel, Luis A. Ladino, Kathy Law, Maurice Levasseur, Quentin Libois, John Liggio, Martine Lizotte, Katrina M. Macdonald, Rashed Mahmood, Randall V. Martin, Ryan H. Mason, Lisa A. Miller, Alexander Moravek, Eric Mortenson, Emma L. Mungall, Jennifer G. Murphy, Maryam Namazi, Ann-Lise Norman, Norman T. O'Neill, Jeffrey R. Pierce, Lynn M. Russell, Johannes Schneider, Hannes Schulz, Sangeeta Sharma, Meng Si, Ralf M. Staebler, Nadja S. Steiner, Jennie L. Thomas, Knut von Salzen, Jeremy J. B. Wentzell, Megan D. Willis, Gregory R. Wentworth, Jun-Wei Xu, and Jacqueline D. Yakobi-Hancock
Atmos. Chem. Phys., 19, 2527–2560, https://doi.org/10.5194/acp-19-2527-2019, https://doi.org/10.5194/acp-19-2527-2019, 2019
Short summary
Short summary
The Arctic is experiencing considerable environmental change with climate warming, illustrated by the dramatic decrease in sea-ice extent. It is important to understand both the natural and perturbed Arctic systems to gain a better understanding of how they will change in the future. This paper summarizes new insights into the relationships between Arctic aerosol particles and climate, as learned over the past five or so years by a large Canadian research consortium, NETCARE.
Tommaso F. Villa, Reece A. Brown, E. Rohan Jayaratne, L. Felipe Gonzalez, Lidia Morawska, and Zoran D. Ristovski
Atmos. Meas. Tech., 12, 691–702, https://doi.org/10.5194/amt-12-691-2019, https://doi.org/10.5194/amt-12-691-2019, 2019
Short summary
Short summary
This research demonstrates the use of an unmanned aerial vehicle (UAV) to characterize the gaseous and diesel particle emissions of a ship at sea. The field study was part of the research voyage “The Great Barrier Reef as a significant source of climatically relevant aerosol particles” on board the RV Investigator around the Australian Great Barrier Reef. Measurements of the RV Investigator exhaust plume were carried out while the ship was operating at sea, at a steady engine load.
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.
Robin Bénard, Maurice Levasseur, Michael Scarratt, Marie-Amélie Blais, Alfonso Mucci, Gustavo Ferreyra, Michel Starr, Michel Gosselin, Jean-Éric Tremblay, and Martine Lizotte
Biogeosciences, 15, 4883–4904, https://doi.org/10.5194/bg-15-4883-2018, https://doi.org/10.5194/bg-15-4883-2018, 2018
Short summary
Short summary
We investigated the combined effect of ocean acidification and warming on the dynamics of the phytoplankton fall boom in the Lower St. Lawrence Estuary, Canada. Twelve 2600 L mesocosms were used to cover a wide range of pH and two temperatures. We found that warming, rather than acidification, is more likely to alter the autumnal bloom in this estuary in the decades to come by stimulating the development and senescence of diatoms, and promoting picocyanobacteria proliferation.
Joel Alroe, Luke T. Cravigan, Marc D. Mallet, Zoran D. Ristovski, Branka Miljevic, Chiemeriwo G. Osuagwu, and Graham R. Johnson
Atmos. Meas. Tech., 11, 4361–4372, https://doi.org/10.5194/amt-11-4361-2018, https://doi.org/10.5194/amt-11-4361-2018, 2018
Short summary
Short summary
This study describes a new volatility-based method to directly examine the composition and corresponding hygroscopic contribution of mixed aerosol components. Measurements of chamber-generated secondary organic aerosol and coastal marine aerosol demonstrated effective separation of both internal and external mixtures. In each case, the findings enabled composition-based models to reliably reproduce observed particle hygroscopicities.
Margaux Gourdal, Martine Lizotte, Guillaume Massé, Michel Gosselin, Michel Poulin, Michael Scarratt, Joannie Charette, and Maurice Levasseur
Biogeosciences, 15, 3169–3188, https://doi.org/10.5194/bg-15-3169-2018, https://doi.org/10.5194/bg-15-3169-2018, 2018
Short summary
Short summary
Melt ponds (MP) forming over first year ice (FYI) represent a potential source of the climate-relevant gas dimethylsulfide (DMS) to the atmosphere. Nine MP were sampled in the Canadian Arctic Archipelago. DMS concentrations reaching up to 6 nmol L−1, twice the world's surface oceanic mean, were measured. Seawater intrusion appeared to seed MP with DMS-producing communities. DMS flux from Arctic MP is expected to increase in response to the expanding areal and temporal trends of MP on FYI.
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.
Tereza Jarníková, John Dacey, Martine Lizotte, Maurice Levasseur, and Philippe Tortell
Biogeosciences, 15, 2449–2465, https://doi.org/10.5194/bg-15-2449-2018, https://doi.org/10.5194/bg-15-2449-2018, 2018
Short summary
Short summary
This paper presents some of the first high-resolution measurements of a biologically-produced climate-active sulfur gas (dimethylsulfide – DMS) ever made in the Canadian Arctic, taken using two novel high-resolution sampling techniques aboard an icebreaker in the summer of 2015. We show increased concentrations of DMS and its precursors in frontal zones and areas of high sea ice accumulation. Our results provide a snapshot of climate-active gas dynamics in a rapidly changing Arctic.
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.
Douglas B. Collins, Julia Burkart, Rachel Y.-W. Chang, Martine Lizotte, Aude Boivin-Rioux, Marjolaine Blais, Emma L. Mungall, Matthew Boyer, Victoria E. Irish, Guillaume Massé, Daniel Kunkel, Jean-Éric Tremblay, Tim Papakyriakou, Allan K. Bertram, Heiko Bozem, Michel Gosselin, Maurice Levasseur, and Jonathan P. D. Abbatt
Atmos. Chem. Phys., 17, 13119–13138, https://doi.org/10.5194/acp-17-13119-2017, https://doi.org/10.5194/acp-17-13119-2017, 2017
Short summary
Short summary
The sources of aerosol particles and their growth to sizes large enough to act as cloud droplet seeds is of major importance to climate since clouds exert substantial control over the atmospheric energy balance. Using ship-board measurements from two summers in the Canadian Arctic, aerosol formation events were related to co-sampled atmospheric and oceanic parameters, providing insight into factors that drive particle formation and motivating further study of ocean–atmosphere interactions.
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.
Victoria E. Irish, Pablo Elizondo, Jessie Chen, Cédric Chou, Joannie Charette, Martine Lizotte, Luis A. Ladino, Theodore W. Wilson, Michel Gosselin, Benjamin J. Murray, Elena Polishchuk, Jonathan P. D. Abbatt, Lisa A. Miller, and Allan K. Bertram
Atmos. Chem. Phys., 17, 10583–10595, https://doi.org/10.5194/acp-17-10583-2017, https://doi.org/10.5194/acp-17-10583-2017, 2017
Short summary
Short summary
The ocean is a possible source of atmospheric ice-nucleating particles (INPs). In this study we found that INPs were ubiquitous in the sea-surface microlayer and bulk seawater in the Canadian Arctic. A strong negative correlation was observed between salinity and freezing temperatures (after correcting for freezing point depression). Heat and filtration treatments of the samples showed that the INPs were likely biological material with sizes between 0.02 μm and 0.2 μm in diameter.
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.
Hakase Hayashida, Nadja Steiner, Adam Monahan, Virginie Galindo, Martine Lizotte, and Maurice Levasseur
Biogeosciences, 14, 3129–3155, https://doi.org/10.5194/bg-14-3129-2017, https://doi.org/10.5194/bg-14-3129-2017, 2017
Short summary
Short summary
In remote regions, cloud conditions may be strongly influenced by oceanic source of dimethylsulfide (DMS) produced by plankton and bacteria. In the Arctic, sea ice provides an additional source of these aerosols. The results of this study highlight the importance of taking into account both the sea-ice sulfur cycle and ecosystem in the flux estimates of oceanic DMS near the ice margins and identify key uncertainties in processes and rates that would be better constrained by new observations.
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.
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
Short summary
Short summary
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.
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.
Marc D. Mallet, Luke T. Cravigan, Andelija Milic, Joel Alroe, Zoran D. Ristovski, Jason Ward, Melita Keywood, Leah R. Williams, Paul Selleck, and Branka Miljevic
Atmos. Chem. Phys., 17, 3605–3617, https://doi.org/10.5194/acp-17-3605-2017, https://doi.org/10.5194/acp-17-3605-2017, 2017
Short summary
Short summary
This paper presents data on the size, composition and concentration of aerosol particles emitted from north Australian savannah fires and how these properties influence cloud condensation nuclei (CCN) concentrations. Both the size and composition of aerosol were found to be important in determining CCN. Despite large CCNc enhancements during periods of close biomass burning, the aerosol was very weakly hygroscopic which should be accounted for in climate models to avoid large CCNc overestimates.
Farhad Salimi, Md. Mahmudur Rahman, Sam Clifford, Zoran Ristovski, and Lidia Morawska
Atmos. Chem. Phys., 17, 521–530, https://doi.org/10.5194/acp-17-521-2017, https://doi.org/10.5194/acp-17-521-2017, 2017
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.
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
Short summary
Short summary
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.
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.
Emma L. Mungall, Betty Croft, Martine Lizotte, Jennie L. Thomas, Jennifer G. Murphy, Maurice Levasseur, Randall V. Martin, Jeremy J. B. Wentzell, John Liggio, and Jonathan P. D. Abbatt
Atmos. Chem. Phys., 16, 6665–6680, https://doi.org/10.5194/acp-16-6665-2016, https://doi.org/10.5194/acp-16-6665-2016, 2016
Short summary
Short summary
Previous work has suggested that marine emissions of dimethyl sulfide (DMS) could impact the Arctic climate through interactions with clouds. We made the first high-time-resolution measurements of summertime atmospheric DMS in the Canadian Arctic, and performed source sensitivity simulations. We found that regional marine sources dominated, but do not appear to be sufficient to explain our observations. Understanding DMS sources in the Arctic is necessary to model future climate in the region.
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.
Josiane Mélançon, Maurice Levasseur, Martine Lizotte, Michael Scarratt, Jean-Éric Tremblay, Philippe Tortell, Gui-Peng Yang, Guang-Yu Shi, Huiwang Gao, David Semeniuk, Marie Robert, Michael Arychuk, Keith Johnson, Nes Sutherland, Marty Davelaar, Nina Nemcek, Angelica Peña, and Wendy Richardson
Biogeosciences, 13, 1677–1692, https://doi.org/10.5194/bg-13-1677-2016, https://doi.org/10.5194/bg-13-1677-2016, 2016
Short summary
Short summary
Ocean acidification is likely to affect iron-limited phytoplankton fertilization by desert dust. Short incubations of northeast subarctic Pacific waters enriched with dust and set at pH 8.0 and 7.8 were conducted. Acidification led to a significant reduction (by 16–38 %) of the final concentration of chl a reached after enrichment. These results show that dust deposition events in a low-pH iron-limited ocean are likely to stimulate phytoplankton growth to a lesser extent than in today's ocean.
F. Salimi, L. R. Crilley, S. Stevanovic, Z. Ristovski, M. Mazaheri, C. He, G. Johnson, G. Ayoko, and L. Morawska
Atmos. Chem. Phys., 15, 13475–13485, https://doi.org/10.5194/acp-15-13475-2015, https://doi.org/10.5194/acp-15-13475-2015, 2015
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.
A. M. Pourkhesalian, S. Stevanovic, M. M. Rahman, E. M. Faghihi, S. E. Bottle, A. R. Masri, R. J. Brown, and Z. D. Ristovski
Atmos. Chem. Phys., 15, 9099–9108, https://doi.org/10.5194/acp-15-9099-2015, https://doi.org/10.5194/acp-15-9099-2015, 2015
Short summary
Short summary
This study investigates the effects of biodiesel's chemical composition on the volatility and reactive oxygenate species of fresh and aged diesel particulate matter.
Using a potential aerosol mass chamber, changes of volatility and reactive oxygenated species are studied. The study concludes that more saturated and more oxygenated diesel fuels can cause more volatile particles carrying more reactive oxygenated species whether before or after aging.
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.
F. Salimi, Z. Ristovski, M. Mazaheri, R. Laiman, L. R. Crilley, C. He, S. Clifford, and L. Morawska
Atmos. Chem. Phys., 14, 11883–11892, https://doi.org/10.5194/acp-14-11883-2014, https://doi.org/10.5194/acp-14-11883-2014, 2014
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. Tjernström, C. Leck, C. E. Birch, J. W. Bottenheim, B. J. Brooks, I. M. Brooks, L. Bäcklin, R. Y.-W. Chang, G. de Leeuw, L. Di Liberto, S. de la Rosa, E. Granath, M. Graus, A. Hansel, J. Heintzenberg, A. Held, A. Hind, P. Johnston, J. Knulst, M. Martin, P. A. Matrai, T. Mauritsen, M. Müller, S. J. Norris, M. V. Orellana, D. A. Orsini, J. Paatero, P. O. G. Persson, Q. Gao, C. Rauschenberg, Z. Ristovski, J. Sedlar, M. D. Shupe, B. Sierau, A. Sirevaag, S. Sjogren, O. Stetzer, E. Swietlicki, M. Szczodrak, P. Vaattovaara, N. Wahlberg, M. Westberg, and C. R. Wheeler
Atmos. Chem. Phys., 14, 2823–2869, https://doi.org/10.5194/acp-14-2823-2014, https://doi.org/10.5194/acp-14-2823-2014, 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: Aerosols | Research Activity: Field Measurements | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Measurement report: In-depth characterization of ship emissions during operations in a Mediterranean port
Direct measurement of N2O5 heterogeneous uptake coefficients on atmospheric aerosols in southwestern China and evaluation of current parameterizations
Measurement report: Per- and polyfluoroalkyl substances (PFAS) in particulate matter (PM10) from activated sludge aeration
African dust transported to Barbados in the wintertime lacks indicators of chemical aging
A 60-year atmospheric nitrate isotope record from a southeastern Greenland ice core with minimal postdepositional alteration
Measurement report: Characterization of aerosol hygroscopicity over Southeast Asia during the NASA CAMP2Ex campaign
Molecular characterization of organic aerosols in urban and forested areas of Paris using high-resolution mass spectrometry
Measurement report: Wintertime aerosol characterization at an urban traffic site in Helsinki, Finland
Source apportionment and ecotoxicity of PM2.5 pollution events in a major Southern Hemisphere megacity: influence of a biofuel-impacted fleet and biomass burning
Marine organic aerosol at Mace Head: effects from phytoplankton and source region variability
Fossil-Dominated SOA Formation in Coastal China: Size-Divergent Pathways of Aqueous Fenton Reactions versus Gas-phase VOC Autoxidation
Measurement report: Sources and meteorology influencing highly time-resolved PM2.5 trace elements at three urban sites in the extremely polluted Indo-Gangetic Plain in India
Formation of highly absorptive secondary brown carbon through nighttime multiphase chemistry of biomass burning emissions
Measurement report: Vertically resolved atmospheric properties observed over the Southern Great Plains with the ArcticShark uncrewed aerial system
Technical note: Towards a stronger observational support for haze pollution control by interpreting carbonaceous aerosol results derived from different measurement approaches
Non-biogenic sources are an important but overlooked contributor to aerosol isoprene-derived organosulfates during winter in northern China
Unveiling single-particle composition, size, shape, and mixing state of freshly emitted Icelandic dust via electron microscopy analysis
The critical role of aqueous-phase processes in aromatic-derived nitrogen-containing organic aerosol formation in cities with different energy consumption patterns
Characterization of atmospheric water-soluble brown carbon in the Athabasca oil sands region, Canada
Sensitivity of aerosol and cloud properties to coupling strength of marine boundary layer clouds over the northwest Atlantic
Measurement Report: Molecular composition, sources, and evolution of atmospheric organic aerosols in a basin city in China
Burning conditions and transportation pathways determine biomass-burning aerosol properties in the Ascension Island marine boundary layer
Observations of high-time-resolution and size-resolved aerosol chemical composition and microphysics in the central Arctic: implications for climate-relevant particle properties
Measurement report: Brown carbon aerosol in rural Germany – sources, chemistry, and diurnal variations
Particle flux-gradient relationships in the high Arctic: Emission and deposition patterns across three surface types
Climatology of aerosol pH and its controlling factors at the Melpitz continental background site in central Europe
Measurement Report: Polycyclic aromatic hydrocarbons (PAHs) and their alkylated (RPAHs), nitrated (NPAHs) and oxygenated (OPAHs) derivatives in the global marine atmosphere: occurrence, spatial variations, and source apportionment
Multiple eco-regions contribute to the seasonal cycle of Antarctic aerosol size distributions
Seasonal investigation of ultrafine-particle organic composition in an eastern Amazonian rainforest
Characterizing lead-rich particles in Beijing's atmosphere following coal-to-gas conversion: Insights from single particle aerosol mass spectrometry
Contrasting solubility and speciation of metal ions in total suspended particulate matter and fog from the coast of Namibia
Significant secondary formation of nitrogenous organic aerosols in an urban atmosphere revealed by bihourly measurements of bulk organic nitrogen and comprehensive molecular markers
High-resolution analyses of concentrations and sizes of refractory black carbon particles deposited in northwestern Greenland over the past 350 years – Part 2: Seasonal and temporal trends in refractory black carbon originated from fossil fuel combustion and biomass burning
Carbonate content and stable isotopic composition of aerosol carbon in the Canadian High Arctic
Significant role of biomass burning in heavy haze formation in Nanjing, a megacity in China: molecular-level insights from intensive PM2.5 sampling on winter hazy days
Widespread trace bromine and iodine in remote tropospheric non-sea-salt aerosols
Significant contributions of biomass burning to PM2.5-bound aromatic compounds: insights from field observations and quantum chemical calculations
Iron isotopes reveal significant aerosol dissolution over the Pacific Ocean
Formation and chemical evolution of secondary organic aerosol in two different environments: a dual-chamber study
Complementary aerosol mass spectrometry elucidates sources of wintertime sub-micron particle pollution in Fairbanks, Alaska, during ALPACA 2022
Enrichment of organic nitrogen in fog residuals observed in the Italian Po Valley
Technical note: Quantified organic aerosol subsaturated hygroscopicity by a simple optical scatter monitor system through field measurements
Measurement report: Oxidation potential of water-soluble aerosol components in the south and north of Beijing
Enhanced daytime secondary aerosol formation driven by gas–particle partitioning in downwind urban plumes
Technical note: Reconstructing surface missing aerosol elemental carbon data in long-term series with ensemble learning
Understanding the mechanism and importance of brown carbon bleaching across the visible spectrum in biomass burning plumes from the WE-CAN campaign
Influence of terrestrial and marine air mass on the constituents and intermixing of bioaerosols over a coastal atmosphere
A multi-site passive approach to studying the emissions and evolution of smoke from prescribed fires
The annual cycle and sources of relevant aerosol precursor vapors in the central Arctic during the MOSAiC expedition
Enhanced emission of intermediate/semi-volatile organic matters in both gas and particle phases from ship exhausts with low-sulfur fuels
Lise Le Berre, Brice Temime-Roussel, Grazia Maria Lanzafame, Barbara D'Anna, Nicolas Marchand, Stéphane Sauvage, Marvin Dufresne, Liselotte Tinel, Thierry Leonardis, Joel Ferreira de Brito, Alexandre Armengaud, Grégory Gille, Ludovic Lanzi, Romain Bourjot, and Henri Wortham
Atmos. Chem. Phys., 25, 6575–6605, https://doi.org/10.5194/acp-25-6575-2025, https://doi.org/10.5194/acp-25-6575-2025, 2025
Short summary
Short summary
A summer campaign in a Mediterranean port examined pollution caused by ships. Two stations in the port measured pollution levels and captured over 350 ship plumes to study their chemical composition. Results showed that pollution levels, such as ultra-fine particles, were higher in the port than in the city and offer strong support to improve emission inventories. These findings may also serve as reference to assess the benefits of a sulfur Emission Control Area in the Mediterranean in 2025.
Jiayin Li, Tianyu Zhai, Xiaorui Chen, Haichao Wang, Shuyang Xie, Shiyi Chen, Chunmeng Li, Yuanjun Gong, Huabin Dong, and Keding Lu
Atmos. Chem. Phys., 25, 6395–6406, https://doi.org/10.5194/acp-25-6395-2025, https://doi.org/10.5194/acp-25-6395-2025, 2025
Short summary
Short summary
We directly measured the dinitrogen pentoxide (N2O5) uptake coefficient using an aerosol flow tube, which critically impacts the NOx fate and particulate nitrate formation in a typical highland city, Kunming, in China. We found that the performance of current γ (N2O5) parameterizations showed deviations with the varying aerosol liquid water content (ALWC). Such differences would lead to biased estimation of particulate nitrate production potential. We give suggestions for future research directions.
Jishnu Pandamkulangara Kizhakkethil, Zongbo Shi, Anna Bogush, and Ivan Kourtchev
Atmos. Chem. Phys., 25, 5947–5958, https://doi.org/10.5194/acp-25-5947-2025, https://doi.org/10.5194/acp-25-5947-2025, 2025
Short summary
Short summary
Pollution with per- and polyfluoroalkyl substances (PFAS) has received attention due to their environmental persistence and bioaccumulation, but their sources remain poorly understood. PM10 (particulate matter) collected above a scaled-down activated sludge tank treating domestic sewage in the UK was analysed for a range of short-, medium-, and long-chain PFAS. Eight PFAS were detected in the PM10. Our results suggest that wastewater treatment processes, i.e. activated sludge aeration, could aerosolise PFAS into airborne PM.
Haley M. Royer, Michael T. Sheridan, Hope E. Elliott, Edmund Blades, Nurun Nahar Lata, Zezhen Cheng, Swarup China, Zihua Zhu, Andrew P. Ault, and Cassandra J. Gaston
Atmos. Chem. Phys., 25, 5743–5759, https://doi.org/10.5194/acp-25-5743-2025, https://doi.org/10.5194/acp-25-5743-2025, 2025
Short summary
Short summary
Saharan dust transported across the Atlantic to the Caribbean, South America, and North America is hypothesized to undergo chemical processing by acids that enhances cloud droplet formation and nutrient availability. In this study, chemical analysis performed on African dust deposited over Barbados shows that acid tracers are found mostly on sea salt and smoke particles, rather than dust, indicating that dust particles undergo minimal chemical processing.
Zhao Wei, Shohei Hattori, Asuka Tsuruta, Zhuang Jiang, Sakiko Ishino, Koji Fujita, Sumito Matoba, Lei Geng, Alexis Lamothe, Ryu Uemura, Naohiro Yoshida, Joel Savarino, and Yoshinori Iizuka
Atmos. Chem. Phys., 25, 5727–5742, https://doi.org/10.5194/acp-25-5727-2025, https://doi.org/10.5194/acp-25-5727-2025, 2025
Short summary
Short summary
Nitrate isotope records in ice cores reveal changes in NOₓ emissions and atmospheric oxidation chemistry driven by human activity. However, UV-driven postdepositional processes can alter nitrate in snow, making snow accumulation rates critical for preserving these records. This study examines nitrate isotopes in a southeastern Greenland ice core, where high snow accumulation minimizes these effects, providing a reliable archive of atmospheric nitrogen cycling.
Genevieve Rose Lorenzo, Luke D. Ziemba, Avelino F. Arellano, Mary C. Barth, Ewan C. Crosbie, Joshua P. DiGangi, Glenn S. Diskin, Richard Ferrare, Miguel Ricardo A. Hilario, Michael A. Shook, Simone Tilmes, Jian Wang, Qian Xiao, Jun Zhang, and Armin Sorooshian
Atmos. Chem. Phys., 25, 5469–5495, https://doi.org/10.5194/acp-25-5469-2025, https://doi.org/10.5194/acp-25-5469-2025, 2025
Short summary
Short summary
Novel aerosol hygroscopicity analyses of CAMP2Ex (Cloud, Aerosol, and Monsoon Processes Philippines Experiment) field campaign data show low aerosol hygroscopicity values in Southeast Asia. Organic carbon from smoke decreases hygroscopicity to levels more like those in continental than in polluted marine regions. Hygroscopicity changes at cloud level demonstrate how surface particles impact clouds in the region, affecting model representation of aerosol and cloud interactions in similar polluted marine regions with high organic carbon emissions.
Diana L. Pereira, Chiara Giorio, Aline Gratien, Alexander Zherebker, Gael Noyalet, Servanne Chevaillier, Stéphanie Alage, Elie Almarj, Antonin Bergé, Thomas Bertin, Mathieu Cazaunau, Patrice Coll, Ludovico Di Antonio, Sergio Harb, Johannes Heuser, Cécile Gaimoz, Oscar Guillemant, Brigitte Language, Olivier Lauret, Camilo Macias, Franck Maisonneuve, Bénédicte Picquet-Varrault, Raquel Torres, Sylvain Triquet, Pascal Zapf, Lelia Hawkins, Drew Pronovost, Sydney Riley, Pierre-Marie Flaud, Emilie Perraudin, Pauline Pouyes, Eric Villenave, Alexandre Albinet, Olivier Favez, Robin Aujay-Plouzeau, Vincent Michoud, Christopher Cantrell, Manuela Cirtog, Claudia Di Biagio, Jean-François Doussin, and Paola Formenti
Atmos. Chem. Phys., 25, 4885–4905, https://doi.org/10.5194/acp-25-4885-2025, https://doi.org/10.5194/acp-25-4885-2025, 2025
Short summary
Short summary
In order to study aerosols in environments influenced by anthropogenic and biogenic emissions, we performed analyses of samples collected during the ACROSS (Atmospheric Chemistry Of the Suburban Forest) campaign in summer 2022 in the greater Paris area. After analysis of the chemical composition by means of total carbon determination and high-resolution mass spectrometry, this work highlights the influence of anthropogenic inputs on the chemical composition of both urban and forested areas.
Kimmo Teinilä, Sanna Saarikoski, Henna Lintusaari, Teemu Lepistö, Petteri Marjanen, Minna Aurela, Heidi Hellén, Toni Tykkä, Markus Lampimäki, Janne Lampilahti, Luis Barreira, Timo Mäkelä, Leena Kangas, Juha Hatakka, Sami Harni, Joel Kuula, Jarkko V. Niemi, Harri Portin, Jaakko Yli-Ojanperä, Ville Niemelä, Milja Jäppi, Katrianne Lehtipalo, Joonas Vanhanen, Liisa Pirjola, Hanna E. Manninen, Tuukka Petäjä, Topi Rönkkö, and Hilkka Timonen
Atmos. Chem. Phys., 25, 4907–4928, https://doi.org/10.5194/acp-25-4907-2025, https://doi.org/10.5194/acp-25-4907-2025, 2025
Short summary
Short summary
Physical and chemical properties of particulate matter and concentrations of trace gases were measured in a street canyon in Helsinki, Finland, and an urban background site in January–February 2022 to investigate the effect of wintertime conditions on pollutants. State-of-the-art instruments and a mobile laboratory were used, and the measurement data were analysed further with modelling tools like positive matrix factorization and the Pollution Detection Algorithm.
Guilherme Martins Pereira, Leonardo Yoshiaki Kamigauti, Rubens Fabio Pereira, Djacinto Monteiro dos Santos, Thayná da Silva Santos, José Vinicius Martins, Célia Alves, Cátia Gonçalves, Ismael Casotti Rienda, Nora Kováts, Thiago Nogueira, Luciana Rizzo, Paulo Artaxo, Regina Maura de Miranda, Marcia Akemi Yamasoe, Edmilson Dias de Freitas, Pérola de Castro Vasconcellos, and Maria de Fatima Andrade
Atmos. Chem. Phys., 25, 4587–4616, https://doi.org/10.5194/acp-25-4587-2025, https://doi.org/10.5194/acp-25-4587-2025, 2025
Short summary
Short summary
The chemical composition of fine particulate matter was studied in the megacity of São Paulo (Brazil) during a polluted period. Vehicular-related sources remain relevant; however, a high contribution of biomass burning was observed and correlated with sample ecotoxicity. Emerging biomass burning sources, such as forest fires and sugarcane-bagasse-based power plants, highlight the need for additional control measures alongside stricter rules concerning vehicular emissions.
Emmanuel Chevassus, Kirsten N. Fossum, Darius Ceburnis, Lu Lei, Chunshui Lin, Wei Xu, Colin O'Dowd, and Jurgita Ovadnevaite
Atmos. Chem. Phys., 25, 4107–4129, https://doi.org/10.5194/acp-25-4107-2025, https://doi.org/10.5194/acp-25-4107-2025, 2025
Short summary
Short summary
This study presents the first source apportionment of organic aerosol at Mace Head via high-resolution mass spectrometry. Introducing transfer entropy as a novel method reveals that aged organic aerosol originates from both open-ocean ozonolysis and local peat-burning oxidation. Methanesulfonic acid and organic sea spray both mirror phytoplankton activity, with the former closely tied to coccolithophore blooms and the latter linked to diatoms, chlorophytes, and cyanobacteria.
Jia-Yuan Wang, Meng-Xue Tang, Shan Lu, Ke-Jin Tang, Xing Peng, Ling-Yan He, and Xiao-Feng Huang
EGUsphere, https://doi.org/10.5194/egusphere-2025-1034, https://doi.org/10.5194/egusphere-2025-1034, 2025
Short summary
Short summary
Our study explores how secondary organic aerosols (SOA), a major component of air pollution, form in different particle sizes in a coastal city in China. We found that SOA in fine particles is mainly produced through aqueous chemical reactions, especially those involving iron. In contrast, coarse particles form SOA through reactions with ozone and gases from both fossil fuels and natural sources. These findings highlight the need for size-specific air pollution models.
Ashutosh K. Shukla, Sachchida N. Tripathi, Shamitaksha Talukdar, Vishnu Murari, Sreenivas Gaddamidi, Manousos-Ioannis Manousakas, Vipul Lalchandani, Kuldeep Dixit, Vinayak M. Ruge, Peeyush Khare, Mayank Kumar, Vikram Singh, Neeraj Rastogi, Suresh Tiwari, Atul K. Srivastava, Dilip Ganguly, Kaspar Rudolf Daellenbach, and André S. H. Prévôt
Atmos. Chem. Phys., 25, 3765–3784, https://doi.org/10.5194/acp-25-3765-2025, https://doi.org/10.5194/acp-25-3765-2025, 2025
Short summary
Short summary
Our study delves into the elemental composition of aerosols at three sites across the Indo-Gangetic Plain (IGP), revealing distinct patterns during pollution episodes. We found significant increases in chlorine (Cl)-rich and solid fuel combustion (SFC) sources, indicating dynamic emission sources, agricultural burning impacts, and meteorological influences. Surges in Cl-rich particles during cold periods highlight their role in particle growth under high-relative-humidity conditions.
Ye Kuang, Biao Luo, Shan Huang, Junwen Liu, Weiwei Hu, Yuwen Peng, Duohong Chen, Dingli Yue, Wanyun Xu, Bin Yuan, and Min Shao
Atmos. Chem. Phys., 25, 3737–3752, https://doi.org/10.5194/acp-25-3737-2025, https://doi.org/10.5194/acp-25-3737-2025, 2025
Short summary
Short summary
This research reveals the potential importance of nighttime NO3 radical chemistry and aerosol water in the rapid formation of secondary brown carbon from diluted biomass burning emissions. The findings enhance our understanding of nighttime biomass burning evolution and its implications for climate and regional air quality, especially regarding interactions with background aerosol water and water-rich fogs and clouds.
Fan Mei, Qi Zhang, Damao Zhang, Jerome D. Fast, Gourihar Kulkarni, Mikhail S. Pekour, Christopher R. Niedek, Susanne Glienke, Israel Silber, Beat Schmid, Jason M. Tomlinson, Hardeep S. Mehta, Xena Mansoura, Zezhen Cheng, Gregory W. Vandergrift, Nurun Nahar Lata, Swarup China, and Zihua Zhu
Atmos. Chem. Phys., 25, 3425–3444, https://doi.org/10.5194/acp-25-3425-2025, https://doi.org/10.5194/acp-25-3425-2025, 2025
Short summary
Short summary
This study highlights the unique capability of the ArcticShark, an uncrewed aerial system, in measuring vertically resolved atmospheric properties. Data from 32 research flights in 2023 reveal seasonal patterns and correlations with conventional measurements. The consistency and complementarity of in situ and remote sensing methods are highlighted. The study demonstrates the ArcticShark’s versatility in bridging data gaps and improving the understanding of vertical atmospheric structures.
Yuan Cheng, Ying-jie Zhong, Zhi-qing Zhang, Xu-bing Cao, and Jiu-meng Liu
EGUsphere, https://doi.org/10.5194/egusphere-2025-537, https://doi.org/10.5194/egusphere-2025-537, 2025
Short summary
Short summary
As an emerging hotspot of atmospheric sciences, Northeast China is distinct due to the frigid winter and the strong emissions from agricultural fires. Based on field campaigns conducted in Harbin, we successively identified the analytical method that could lead to proper results of organic and elemental carbon. Our results are believed to be a support for future efforts on exploration of the PM2.5 sources in Northeast China, which are essential for further improving the regional air quality.
Ting Yang, Yu Xu, Yu-Chen Wang, Yi-Jia Ma, Hong-Wei Xiao, Hao Xiao, and Hua-Yun Xiao
Atmos. Chem. Phys., 25, 2967–2978, https://doi.org/10.5194/acp-25-2967-2025, https://doi.org/10.5194/acp-25-2967-2025, 2025
Short summary
Short summary
Previous measurement–model comparisons of atmospheric isoprene levels showed a significant unidentified source of isoprene in some northern Chinese cities during winter. Here, the first combination of large-scale observations and field combustion experiments provides novel insights into biomass burning emissions as a significant source of isoprene-derived organosulfates during winter in northern cities of China.
Agnesh Panta, Konrad Kandler, Kerstin Schepanski, Andres Alastuey, Pavla Dagsson Waldhauserova, Sylvain Dupont, Melanie Eknayan, Cristina González-Flórez, Adolfo González-Romero, Martina Klose, Mara Montag, Xavier Querol, Jesús Yus-Díez, and Carlos Pérez García-Pando
EGUsphere, https://doi.org/10.5194/egusphere-2025-494, https://doi.org/10.5194/egusphere-2025-494, 2025
Short summary
Short summary
Iceland is among the most active dust source areas in the world. Dust properties are influenced by particle size, mineralogy, shape, and mixing state. This work characterizes freshly emitted individual aerosol particles of Icelandic dust using electron microscopy. Our study provides insights into critical particle-specific information will contribute to better constraining climate models that consider mineralogical variations in their representation of the dust cycle.
Yi-Jia Ma, Yu Xu, Ting Yang, Lin Gui, Hong-Wei Xiao, Hao Xiao, and Hua-Yun Xiao
Atmos. Chem. Phys., 25, 2763–2780, https://doi.org/10.5194/acp-25-2763-2025, https://doi.org/10.5194/acp-25-2763-2025, 2025
Short summary
Short summary
The abundance, potential precursors, and main formation mechanisms of nitrogen-containing organic compounds (NOCs) in PM2.5 during winter were compared among cities with different energy consumption patterns. The aerosol NOC pollution during winter in China is closely associated with the intensity of precursor emissions and the aqueous-phase processes. Our results highlight the importance of emission reduction strategies in controlling aerosol NOCs pollution during winter in China.
Dane Blanchard, Mark Gordon, Duc Huy Dang, Paul Andrew Makar, and Julian Aherne
Atmos. Chem. Phys., 25, 2423–2442, https://doi.org/10.5194/acp-25-2423-2025, https://doi.org/10.5194/acp-25-2423-2025, 2025
Short summary
Short summary
This study offers the first known evaluation of water-soluble brown carbon aerosols in the Athabasca oil sands region (AOSR), Canada. Fluorescence spectroscopy analysis of aerosol samples from five regional sites (collected during the summer of 2021) identified oil sands operations as a measurable brown carbon source. Industrial aerosol emissions were unlikely to impact regional radiative forcing. These findings show that fluorescence spectroscopy can be used to monitor brown carbon in the AOSR.
Kira Zeider, Kayla McCauley, Sanja Dmitrovic, Leong Wai Siu, Yonghoon Choi, Ewan C. Crosbie, Joshua P. DiGangi, Glenn S. Diskin, Simon Kirschler, John B. Nowak, Michael A. Shook, Kenneth L. Thornhill, Christiane Voigt, Edward L. Winstead, Luke D. Ziemba, Paquita Zuidema, and Armin Sorooshian
Atmos. Chem. Phys., 25, 2407–2422, https://doi.org/10.5194/acp-25-2407-2025, https://doi.org/10.5194/acp-25-2407-2025, 2025
Short summary
Short summary
In situ aircraft data collected over the northwest Atlantic Ocean are utilized to compare aerosol conditions and turbulence between near-surface and below-cloud-base altitudes for different regimes of coupling strength between those two levels, along with how cloud microphysical properties vary across those regimes. Stronger coupling yields more homogenous aerosol structure vertically along with higher cloud drop concentrations and sea salt influence in clouds.
Junke Zhang, Xinyi Fu, Chunying Chen, Yunfei Su, Siyu Liu, Luyao Chen, Yubao Chen, Gehui Wang, and Andre S. H. Prevot
EGUsphere, https://doi.org/10.5194/egusphere-2025-92, https://doi.org/10.5194/egusphere-2025-92, 2025
Short summary
Short summary
The 125 organic aerosol (OA) compounds in PM2.5 in winter in Chengdu were measured at the molecular level. OA was dominated by fatty acids, phthalate esters, and anhydrosugars, and were deeply influenced by anthropogenic sources. As pollution worsens: secondary inorganic species and secondary organic carbon (OC) dominated the increase in PM2.5; fatty acids and anhydrosugars dominated the increase in OA; and the contribution of secondary formation and biomass burning to OC increased markedly.
Amie Dobracki, Ernie R. Lewis, Arthur J. Sedlacek III, Tyler Tatro, Maria A. Zawadowicz, and Paquita Zuidema
Atmos. Chem. Phys., 25, 2333–2363, https://doi.org/10.5194/acp-25-2333-2025, https://doi.org/10.5194/acp-25-2333-2025, 2025
Short summary
Short summary
Biomass-burning aerosol is commonly present in the marine boundary layer over the southeast Atlantic Ocean between June and October. Our research indicates that burning conditions, aerosol transport pathways, and prolonged oxidation processes (heterogeneous and aqueous phases) determine the chemical, microphysical, and optical properties of the boundary layer aerosol. Notably, we find that the aerosol optical properties can be estimated from the chemical properties alone.
Benjamin Heutte, Nora Bergner, Hélène Angot, Jakob B. Pernov, Lubna Dada, Jessica A. Mirrielees, Ivo Beck, Andrea Baccarini, Matthew Boyer, Jessie M. Creamean, Kaspar R. Daellenbach, Imad El Haddad, Markus M. Frey, Silvia Henning, Tiia Laurila, Vaios Moschos, Tuukka Petäjä, Kerri A. Pratt, Lauriane L. J. Quéléver, Matthew D. Shupe, Paul Zieger, Tuija Jokinen, and Julia Schmale
Atmos. Chem. Phys., 25, 2207–2241, https://doi.org/10.5194/acp-25-2207-2025, https://doi.org/10.5194/acp-25-2207-2025, 2025
Short summary
Short summary
Limited aerosol measurements in the central Arctic hinder our understanding of aerosol–climate interactions in the region. Our year-long observations of aerosol physicochemical properties during the MOSAiC expedition reveal strong seasonal variations in aerosol chemical composition, where the short-term variability is heavily affected by storms in the Arctic. Local wind-generated particles are shown to be an important source of cloud seeds, especially in autumn.
Feng Jiang, Harald Saathoff, Uzoamaka Ezenobi, Junwei Song, Hengheng Zhang, Linyu Gao, and Thomas Leisner
Atmos. Chem. Phys., 25, 1917–1930, https://doi.org/10.5194/acp-25-1917-2025, https://doi.org/10.5194/acp-25-1917-2025, 2025
Short summary
Short summary
The chemical composition of brown carbon in the particle and gas phase was determined by mass spectrometry. BrC in the gas phase was mainly controlled by secondary formation and particle-to-gas partitioning. BrC in the particle phase was mainly from secondary formation. This work helps to get a better understanding of diurnal variations and the sources of brown carbon aerosol at a rural location in central Europe.
Theresa Mathes, Heather Guy, John Prytherch, Julia Kojoj, Ian Brooks, Sonja Murto, Paul Zieger, Birgit Wehner, Michael Tjernström, and Andreas Held
EGUsphere, https://doi.org/10.5194/egusphere-2025-183, https://doi.org/10.5194/egusphere-2025-183, 2025
Short summary
Short summary
The Arctic is warming faster than the global average and aerosol-cloud-sea-ice interactions are crucial for studying its climate system. During the ARTofMELT Expedition 2023, particle and sensible heat fluxes were measured over multiple surfaces. Wide lead surfaces acted as particle sources with the strongest sensible heat fluxes, while closed ice surfaces acted as a particle sink. This study improves methods to measure these interactions, enhancing our understanding of Arctic climate processes.
Vikram Pratap, Christopher J. Hennigan, Bastian Stieger, Andreas Tilgner, Laurent Poulain, Dominik van Pinxteren, Gerald Spindler, and Hartmut Herrmann
EGUsphere, https://doi.org/10.5194/egusphere-2025-457, https://doi.org/10.5194/egusphere-2025-457, 2025
Short summary
Short summary
In this work, we characterize trends in aerosol pH and its controlling factors over the period of 2010 – 2019 at the Melpitz research station in eastern Germany. We find strong trends in aerosol pH and major inorganic species in response to changing emissions. We conduct a detailed thermodynamic analysis of the aerosol system and discuss implications for controlling PM2.5 in the region.
Rui Li, Yubing Shen, Yumeng Shao, Yining Gao, Ziwei Yao, Qian Liu, Xing Liu, and Guitao Shi
EGUsphere, https://doi.org/10.5194/egusphere-2024-3740, https://doi.org/10.5194/egusphere-2024-3740, 2025
Short summary
Short summary
It is the first time to reveal the global variations of PAHs derivatives in the marine air. We found that marine aerosols in East China Sea (ECS) and Western Pacific (WP) were significantly affected by coal and engine combustion, while those in Bismarck Sea (BS) and East Australian Sea (EAS) were mainly influenced by wildfire and coal combustion. Antarctic Ocean (AO) was dominated by biomass burning and local shipping emissions. This finding help elucidate the mechanism of global PAH cycle.
James Brean, David C. S. Beddows, Eija Asmi, Aki Virkkula, Lauriane L. J. Quéléver, Mikko Sipilä, Floortje Van Den Heuvel, Thomas Lachlan-Cope, Anna Jones, Markus Frey, Angelo Lupi, Jiyeon Park, Young Jun Yoon, Rolf Weller, Giselle L. Marincovich, Gabriela C. Mulena, Roy M. Harrison, and Manuel Dall'Osto
Atmos. Chem. Phys., 25, 1145–1162, https://doi.org/10.5194/acp-25-1145-2025, https://doi.org/10.5194/acp-25-1145-2025, 2025
Short summary
Short summary
Our results emphasise how understanding the geographical variation in surface types across the Antarctic is key to understanding secondary aerosol sources.
Adam E. Thomas, Hayley S. Glicker, Alex B. Guenther, Roger Seco, Oscar Vega Bustillos, Julio Tota, Rodrigo A. F. Souza, and James N. Smith
Atmos. Chem. Phys., 25, 959–977, https://doi.org/10.5194/acp-25-959-2025, https://doi.org/10.5194/acp-25-959-2025, 2025
Short summary
Short summary
We present measurements of the organic composition of ultrafine particles collected from the eastern Amazon, an understudied region that is subjected to increasing human influence. We find that while isoprene chemistry is likely significant for ultrafine-particle growth throughout the year, compounds related to other sources, such as biological-spore emissions and biomass burning, exhibit striking seasonal differences, implying extensive variation in regional ultrafine-particle sources.
Xiufeng Lian, Yongjiang Xu, Fengxian Liu, Long Peng, Xiaodong Hu, Guigang Tang, Xu Dao, Hui Guo, Liwei Wang, Bo Huang, Chunlei Cheng, Lei Li, Guohua Zhang, Xinhui Bi, Xiaofei Wang, Zhen Zhou, and Mei Li
EGUsphere, https://doi.org/10.5194/egusphere-2024-3469, https://doi.org/10.5194/egusphere-2024-3469, 2025
Short summary
Short summary
In this study, we analyzed the mixing state and atmospheric chemical processes of Pb-rich single particles in Beijing. Then, we focused on analyzing the differences in Pb-rich particles between the heating period and non-heating period, as well as the formation mechanism of lead nitrate after coal-to-gas conversion. Our results highlighted the improvement of coal-to-gas conversion on Pb in the particulate.
Chiara Giorio, Anne Monod, Valerio Di Marco, Pierre Herckes, Denise Napolitano, Amy Sullivan, Gautier Landrot, Daniel Warnes, Marika Nasti, Sara D'Aronco, Agathe Gérardin, Nicolas Brun, Karine Desboeufs, Sylvain Triquet, Servanne Chevaillier, Claudia Di Biagio, Francesco Battaglia, Frédéric Burnet, Stuart J. Piketh, Andreas Namwoonde, Jean-François Doussin, and Paola Formenti
EGUsphere, https://doi.org/10.5194/egusphere-2024-4140, https://doi.org/10.5194/egusphere-2024-4140, 2025
Short summary
Short summary
A comparison between the solubility of trace metals in pairs of total suspended particulate (TSP) and fog water samples collected in Henties Bay, Namibia, during the AEROCLO-sA field campaign is presented. We found enhanced solubility of metals in fog samples which we attributed to metal-ligand complexes formation in the early stages of particle activation into droplets which can then remain in a kinetically stable form in fog or lead to the formation of colloidal nanoparticles.
Xu Yu, Min Zhou, Shuhui Zhu, Liping Qiao, Jinjian Li, Yingge Ma, Zijing Zhang, Kezheng Liao, Hongli Wang, and Jian Zhen Yu
EGUsphere, https://doi.org/10.5194/egusphere-2024-4103, https://doi.org/10.5194/egusphere-2024-4103, 2025
Short summary
Short summary
Online measurements of bulk aerosol organic nitrogen (ON), in conjunction with a comprehensive array of source markers, have revealed five emission sources and five potentially significant formation processes of nitrogenous organic aerosols. This study provides first quantitative source analysis of ON aerosol and valuable observational evidence on secondary ON aerosol formation through NH3 and NOx chemistries.
Kumiko Goto-Azuma, Yoshimi Ogawa-Tsukagawa, Kaori Fukuda, Koji Fujita, Motohiro Hirabayashi, Remi Dallmayr, Jun Ogata, Nobuhiro Moteki, Tatsuhiro Mori, Sho Ohata, Yutaka Kondo, Makoto Koike, Sumito Matoba, Moe Kadota, Akane Tsushima, Naoko Nagatsuka, and Teruo Aoki
Atmos. Chem. Phys., 25, 657–683, https://doi.org/10.5194/acp-25-657-2025, https://doi.org/10.5194/acp-25-657-2025, 2025
Short summary
Short summary
Monthly ice core records spanning 350 years from Greenland show trends in refractory black carbon (rBC) concentrations and sizes. rBC levels have increased since the 1870s due to the inflow of anthropogenic rBC, with larger diameters than those from biomass burning (BB) rBC. High summer BB rBC peaks may reduce the ice sheet albedo, but BB rBC showed no increase until the early 2000s. These results are vital for validating aerosol and climate models.
Petr Vodička, Kimitaka Kawamura, Bhagawati Kunwar, Lin Huang, Dhananjay K. Deshmukh, Md. Mozammel Haque, Sangeeta Sharma, and Leonard Barrie
EGUsphere, https://doi.org/10.5194/egusphere-2024-3656, https://doi.org/10.5194/egusphere-2024-3656, 2025
Short summary
Short summary
Carbonate carbon (CC) is not negligible in Arctic total suspended particles (TSP). If not considered, CC biases the contribution of elemental and organic carbon. CC content in TSP was strongly reflected in the δ13C values of total carbon (TC). Carbon contribution from CaCO3 supports strong dependence of CC and δ13C on Ca. Finally, two hypothetical CC sources were identified based on the analysis of air mass back trajectories – dust resuspension and marine microorganisms.
Mingjie Kang, Mengying Bao, Wenhuai Song, Aduburexiati Abulimiti, Changliu Wu, Fang Cao, Sönke Szidat, and Yanlin Zhang
Atmos. Chem. Phys., 25, 73–91, https://doi.org/10.5194/acp-25-73-2025, https://doi.org/10.5194/acp-25-73-2025, 2025
Short summary
Short summary
Reports on molecular-level knowledge of high-temporal-resolution particulate matter ≤2.5 µm in diameter (PM2.5) on hazy days are limited. We investigated various PM2.5 species and their sources. The results show biomass burning (BB) was the main source of organic carbon. Moreover, BB enhanced fungal spore emissions and secondary aerosol formation. The contribution of non-fossil sources increased with increasing haze pollution, suggesting BB may be an important driver of haze events in winter.
Gregory P. Schill, Karl D. Froyd, Daniel M. Murphy, Christina J. Williamson, Charles A. Brock, Tomás Sherwen, Mat J. Evans, Eric A. Ray, Eric C. Apel, Rebecca S. Hornbrook, Alan J. Hills, Jeff Peischl, Thomas B. Ryerson, Chelsea R. Thompson, Ilann Bourgeois, Donald R. Blake, Joshua P. DiGangi, and Glenn S. Diskin
Atmos. Chem. Phys., 25, 45–71, https://doi.org/10.5194/acp-25-45-2025, https://doi.org/10.5194/acp-25-45-2025, 2025
Short summary
Short summary
Using single-particle mass spectrometry, we show that trace concentrations of bromine and iodine are ubiquitous in remote tropospheric aerosol and suggest that aerosols are an important part of the global reactive iodine budget. Comparisons to a global climate model with detailed iodine chemistry are favorable in the background atmosphere; however, the model cannot replicate our measurements near the ocean surface, in biomass burning plumes, and in the stratosphere.
Yanqin Ren, Zhenhai Wu, Fang Bi, Hong Li, Haijie Zhang, Junling Li, Rui Gao, Fangyun Long, Zhengyang Liu, Yuanyuan Ji, and Gehui Wang
EGUsphere, https://doi.org/10.5194/egusphere-2024-3678, https://doi.org/10.5194/egusphere-2024-3678, 2025
Short summary
Short summary
The daily concentrations of Polycyclic aromatic hydrocarbons (PAHs), oxygenated PAHs (OPAHs), and nitrated phenols (NPs) in PM2.5 were all increased during the heating season. Biomass burning was identified to be the primary source of these aromatic compounds, particularly for PAHs. Phenol and nitrobenzene are two main primary precursors for 4NP, with phenol showing lower reaction barriers. P-Cresol was identified as the primary precursor for the formation of 4-methyl-5-nitrocatechol.
Capucine Camin, François Lacan, Catherine Pradoux, Marie Labatut, Anne Johansen, and James W. Murray
EGUsphere, https://doi.org/10.5194/egusphere-2024-3777, https://doi.org/10.5194/egusphere-2024-3777, 2024
Short summary
Short summary
This manuscript presents the chemical composition of aerosols (> 1µm) over the Equatorial and Tropical Pacific Ocean, presenting the first measurements of iron isotopes in aerosols from this region. Iron concentrations and isotopes were determined using a Neptune MC-ICPMS. Our data analysis reveals that a significant portion of the aerosols undergo dissolution and removal during atmospheric transport. These findings contribute to original conclusions about the chemistry and physics of aerosols.
Andreas Aktypis, Dontavious J. Sippial, Christina N. Vasilakopoulou, Angeliki Matrali, Christos Kaltsonoudis, Andrea Simonati, Marco Paglione, Matteo Rinaldi, Stefano Decesari, and Spyros N. Pandis
Atmos. Chem. Phys., 24, 13769–13791, https://doi.org/10.5194/acp-24-13769-2024, https://doi.org/10.5194/acp-24-13769-2024, 2024
Short summary
Short summary
A dual-chamber system was deployed in two different environments (Po Valley, Italy, and Pertouli forest, Greece) to study the potential of ambient air directly injected into the chambers, to form secondary organic aerosol (SOA). In the Po Valley, the system reacts rapidly, forming large amounts of SOA, while in Pertouli the SOA formation chemistry appears to have been practically terminated before the beginning of most experiments, so there is little additional SOA formation potential left.
Amna Ijaz, Brice Temime-Roussel, Benjamin Chazeau, Sarah Albertin, Stephen R. Arnold, Brice Barrett, Slimane Bekki, Natalie Brett, Meeta Cesler-Maloney, Elsa Dieudonne, Kayane K. Dingilian, Javier G. Fochesatto, Jingqiu Mao, Allison Moon, Joel Savarino, William Simpson, Rodney J. Weber, Kathy S. Law, and Barbara D'Anna
EGUsphere, https://doi.org/10.5194/egusphere-2024-3789, https://doi.org/10.5194/egusphere-2024-3789, 2024
Short summary
Short summary
Fairbanks is among the most polluted cities with the highest particulate matter (PM) levels in the US during winters. Highly time-resolved measurements of the sub-micron PM elucidated residential heating with wood and oil and hydrocarbon-like organics from traffic, as well as sulphur-containing organic aerosol, to be the key pollution sources. Remarkable differences existed between complementary instruments, warranting the deployment of multiple tools at sites with wide-ranging influences.
Fredrik Mattsson, Almuth Neuberger, Liine Heikkinen, Yvette Gramlich, Marco Paglione, Matteo Rinaldi, Stefano Decesari, Paul Zieger, Ilona Riipinen, and Claudia Mohr
EGUsphere, https://doi.org/10.5194/egusphere-2024-3629, https://doi.org/10.5194/egusphere-2024-3629, 2024
Short summary
Short summary
This study investigated aerosol-cloud interactions, focusing on organic nitrogen (ON) formation in the aqueous phase. Measurements were conducted in wintertime Italian Po Valley, using aerosol mass spectrometry. The fog was enriched in more hygroscopic inorganic compounds and ON, containing e.g. imidazoles. The formation of imidazole by aerosol-fog interactions could be confirmed for the first time in atmospheric observations. Findings highlight the role of fog in nitrogen aerosol formation.
Jie Zhang, Tianyu Zhu, Alexandra Catena, Yaowei Li, Margaret J. Schwab, Pengfei Liu, Akua Asa-Awuku, and James Schwab
Atmos. Chem. Phys., 24, 13445–13456, https://doi.org/10.5194/acp-24-13445-2024, https://doi.org/10.5194/acp-24-13445-2024, 2024
Short summary
Short summary
This study shows the derived organic aerosol hygroscopicity under high-humidity conditions based on a simple optical scatter monitor system, including two nephelometric monitors (pDR-1500), when the aerosol chemical composition is already known.
Wei Yuan, Ru-Jin Huang, Chao Luo, Lu Yang, Wenjuan Cao, Jie Guo, and Huinan Yang
Atmos. Chem. Phys., 24, 13219–13230, https://doi.org/10.5194/acp-24-13219-2024, https://doi.org/10.5194/acp-24-13219-2024, 2024
Short summary
Short summary
We characterized water-soluble oxidative potential (OP) levels in wintertime PM2.5 in the south and north of Beijing. Our results show that the volume-normalized dithiothreitol (DTTv) in the north was comparable to that in the south, while the mass-normalized dithiothreitol (DTTm) in the north was almost twice that in the south. Traffic-related emissions and biomass burning were the main sources of DTTv in the south, and traffic-related emissions contributed the most to DTTv in the north.
Mingfu Cai, Chenshuo Ye, Bin Yuan, Shan Huang, E Zheng, Suxia Yang, Zelong Wang, Yi Lin, Tiange Li, Weiwei Hu, Wei Chen, Qicong Song, Wei Li, Yuwen Peng, Baoling Liang, Qibin Sun, Jun Zhao, Duohong Chen, Jiaren Sun, Zhiyong Yang, and Min Shao
Atmos. Chem. Phys., 24, 13065–13079, https://doi.org/10.5194/acp-24-13065-2024, https://doi.org/10.5194/acp-24-13065-2024, 2024
Short summary
Short summary
This study investigated the daytime secondary organic aerosol (SOA) formation in urban plumes. We observed a significant daytime SOA formation through gas–particle partitioning when the site was affected by urban plumes. A box model simulation indicated that urban pollutants (nitrogen oxide and volatile organic compounds) could enhance the oxidizing capacity, while the elevated volatile organic compounds were mainly responsible for promoting daytime SOA formation.
Qingxiao Meng, Yunjiang Zhang, Sheng Zhong, Jie Fang, Lili Tang, Yongcai Rao, Minfeng Zhou, Jian Qiu, Xiaofeng Xu, Jean-Eudes Petit, Olivier Favez, and Xinlei Ge
EGUsphere, https://doi.org/10.5194/egusphere-2024-2776, https://doi.org/10.5194/egusphere-2024-2776, 2024
Short summary
Short summary
We developed a new method to reconstruct missing elemental carbon (EC) data in four Chinese cities from 2013 to 2023. Using machine learning, we accurately filled data gaps and introduced a new approach to analyze EC trends. Our findings reveal a significant decline in EC due to stricter pollution controls, though this slowed after 2020. This study provides a versatile framework for addressing data gaps and supports strategies to reduce urban air pollution and its climate impacts.
Yingjie Shen, Rudra P. Pokhrel, Amy P. Sullivan, Ezra J. T. Levin, Lauren A. Garofalo, Delphine K. Farmer, Wade Permar, Lu Hu, Darin W. Toohey, Teresa Campos, Emily V. Fischer, and Shane M. Murphy
Atmos. Chem. Phys., 24, 12881–12901, https://doi.org/10.5194/acp-24-12881-2024, https://doi.org/10.5194/acp-24-12881-2024, 2024
Short summary
Short summary
The magnitude and evolution of brown carbon (BrC) absorption remain unclear, with uncertainty in climate models. Data from the WE-CAN airborne experiment show that model parameterizations overestimate the mass absorption cross section (MAC) of BrC. Observed decreases in BrC absorption with chemical markers are due to decreasing organic aerosol (OA) mass rather than a decreasing BrC MAC, which is currently implemented in models. Water-soluble BrC contributes 23 % of total absorption at 660 nm.
Qun He, Zhaowen Wang, Houfeng Liu, Pengju Xu, Rongbao Duan, Caihong Xu, Jianmin Chen, and Min Wei
Atmos. Chem. Phys., 24, 12775–12792, https://doi.org/10.5194/acp-24-12775-2024, https://doi.org/10.5194/acp-24-12775-2024, 2024
Short summary
Short summary
Coastal environments provide an ideal setting for investigating the intermixing of terrestrial and marine aerosols. Terrestrial air mass constituted a larger number of microbes from anthropogenic and soil emissions, whereas saprophytic and gut microbes were predominant in marine samples. Mixed air masses indicated a fusion of marine and terrestrial aerosols, characterized by alterations in the ratio of pathogenic and saprophytic microbes when compared to either terrestrial or marine samples.
Rime El Asmar, Zongrun Li, David J. Tanner, Yongtao Hu, Susan O'Neill, L. Gregory Huey, M. Talat Odman, and Rodney J. Weber
Atmos. Chem. Phys., 24, 12749–12773, https://doi.org/10.5194/acp-24-12749-2024, https://doi.org/10.5194/acp-24-12749-2024, 2024
Short summary
Short summary
Prescribed burning is an important method for managing ecosystems and preventing wildfires. However, smoke from prescribed fires can have a significant impact on air quality. Here, using a network of fixed sites and sampling throughout an extended prescribed burning period in 2 different years, we characterize emissions and evolutions of up to 8 h of PM2.5 mass, black carbon (BC), and brown carbon (BrC) in smoke from burning of forested lands in the southeastern USA.
Matthew Boyer, Diego Aliaga, Lauriane L. J. Quéléver, Silvia Bucci, Hélène Angot, Lubna Dada, Benjamin Heutte, Lisa Beck, Marina Duetsch, Andreas Stohl, Ivo Beck, Tiia Laurila, Nina Sarnela, Roseline C. Thakur, Branka Miljevic, Markku Kulmala, Tuukka Petäjä, Mikko Sipilä, Julia Schmale, and Tuija Jokinen
Atmos. Chem. Phys., 24, 12595–12621, https://doi.org/10.5194/acp-24-12595-2024, https://doi.org/10.5194/acp-24-12595-2024, 2024
Short summary
Short summary
We analyze the seasonal cycle and sources of gases that are relevant for the formation of aerosol particles in the central Arctic. Since theses gases can form new particles, they can influence Arctic climate. We show that the sources of these gases are associated with changes in the Arctic environment during the year, especially with respect to sea ice. Therefore, the concentration of these gases will likely change in the future as the Arctic continues to warm.
Binyu Xiao, Fan Zhang, Zeyu Liu, Yan Zhang, Rui Li, Can Wu, Xinyi Wan, Yi Wang, Yubao Chen, Yong Han, Min Cui, Libo Zhang, Yingjun Chen, and Gehui Wang
EGUsphere, https://doi.org/10.5194/egusphere-2024-3433, https://doi.org/10.5194/egusphere-2024-3433, 2024
Short summary
Short summary
Intermediate/semi-volatile organic compounds in both gas and particle phases from ship exhausts are enhanced due to the switch of fuels from low-sulfur to ultra-low-sulfur. The findings indicate that optimization is necessary for the forthcoming global implementation of an ultra-low-sulfur oil policy. Besides, we find that organic diagnostic markers of hopanes, in conjunction with the ratio of octadecanoic to tetradecanoic could be considered as potential tracers for HFO exhausts.
Cited articles
Allen, A. G., Dick, A. L., and Davison, B. M.: Sources of atmospheric methanesulphonate, non-sea-salt sulphate, nitrate and related species over the temperate South Pacific, Atmos. Environ., 31, 191–205, https://doi.org/10.1016/1352-2310(96)00194-x, 1997.
Almeida, J., Schobesberger, S., Kürten, A., Ortega, I. K., Kupiainen-Maatta, O., Praplan, A. P., Adamov, A., Amorim, A., Bianchi, F., Breitenlechner, M., David, A., Dommen, J., Donahue, N. M., Downard, A., Dunne, E., Duplissy, J., Ehrhart, S., Flagan, R. C., Franchin, A., Guida, R., Hakala, J., Hansel, A., Heinritzi, M., Henschel, H., Jokinen, T., Junninen, H., Kajos, M., Kangasluoma, J., Keskinen, H., Kupc, A., Kurtén, T., Kvashin, A. N., Laaksonen, A., Lehtipalo, K., Leiminger, M., Leppa, J., Loukonen, V., Makhmutov, V., Mathot, S., McGrath, M. J., Nieminen, T., Olenius, T., Onnela, A., Petäjä, T., Riccobono, F., Riipinen, I., Rissanen, M., Rondo, L., Ruuskanen, T., Santos, F. D., Sarnela, N., Schallhart, S., Schnitzhofer, R., Seinfeld, J. H., Simon, M., Sipilä, M., Stozhkov, Y., Stratmann, F., Tomé, A., Trostl, J., Tsagkogeorgas, G., Vaattovaara, P., Viisanen, Y., Virtanen, A., Vrtala, A., Wagner, P. E., Weingartner, E., Wex, H., Williamson, C., Wimmer, D., Ye, P., Yli-Juuti, T., Carslaw, K. S., Kulmala, M., Curtius, J., Baltensperger, U., Worsnop, D. R., Vehkamaki, H., and Kirkby, J.: Molecular understanding of sulphuric acid-amine particle nucleation in the atmosphere, Nature, 502, 359–363, https://doi.org/10.1038/nature12663, 2013.
Andreae, M. O. and Rosenfeld, D.: Aerosol–cloud–precipitation interactions. Part 1. The nature and sources of cloud-active aerosols, Earth-Sci. Rev., 89, 13–41, https://doi.org/10.1016/j.earscirev.2008.03.001, 2008.
Archer, S. D., Safi, K., Hall, A., Cummings, D. G., and Harvey, M.: Grazing suppression of dimethylsulphoniopropionate (DMSP) accumulation in iron-fertilised, sub-Antarctic waters, Deep-Sea Res. Pt II, 58, 839–850, https://doi.org/10.1016/j.dsr2.2010.10.022, 2011.
Ayers, G. P., Ivey, J. P., and Gillett, R. W.: Coherence between seasonal cycles of dimethylsulfide, methanesulfonate, and sulfate in Marine Air, Nature, 349, 404–406, 1991.
Balch, W. M., Drapeau, D. T., Bowler, B. C., Lyczskowski, E., Booth, E. S., and Alley, D.: The contribution of coccolithophores to the optical and inorganic carbon budgets during the Southern Ocean Gas Exchange Experiment: New evidence in support of the “Great Calcite Belt” hypothesis, J. Geophys. Res.-Oceans, 116, C00F06, https://doi.org/10.1029/2011jc006941, 2011.
Bell, T. G., Malin, G., Lee, G. A., Stefels, J., Archer, S., Steinke, M., and Matrai, P.: Global oceanic DMS data inter-comparability, Biogeochem., 110, 147–161, https://doi.org/10.1007/s10533-011-9662-3, 2012.
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.
Bell, T. G., Landwehr, S., Miller, S. D., de Bruyn, W. J., Callaghan, A. H., Scanlon, B., Ward, B., Yang, M., and Saltzman, E. S.: Estimation of bubble-mediated air–sea gas exchange from concurrent DMS and CO2 transfer velocities at intermediate–high wind speeds, Atmos. Chem. Phys., 17, 9019–9033, https://doi.org/10.5194/acp-17-9019-2017, 2017.
Blake, N. J., Blake, D. R., Wingenter, O. W., Sive, B. C., Kang, C. H., Thornton, D. C., Bandy, A. R., Atlas, E., Flocke, F., Harris, J. M., and Rowland, F. S.: Aircraft measurements of the latitudinal, vertical, and seasonal variations of NMHCs, methyl nitrate, methyl halides, and DMS during the First Aerosol Characterization Experiment (ACE 1), J. Geophys. Res.-Atmos., 104, 21803–21817, https://doi.org/10.1029/1999jd900238, 1999.
Blomquist, B. W., Fairall, C. W., Huebert, B. J., Kieber, D. J., and Westby, G. R.: DMS sea-air transfer velocity: Direct measurements by eddy covariance and parameterization based on the NOAA/COARE gas transfer model, Geophys. Res. Lett., 33, L07601, https://doi.org/10.1029/2006GL025735, 2006.
Blot, R., Clarke, A. D., Freitag, S., Kapustin, V., Howell, S. G., Jensen, J. B., Shank, L. M., McNaughton, C. S., and Brekhovskikh, V.: Ultrafine sea spray aerosol over the southeastern Pacific: open-ocean contributions to marine boundary layer CCN, Atmos. Chem. Phys., 13, 7263–7278, https://doi.org/10.5194/acp-13-7263-2013, 2013.
Boers, R., Jensen, J. B., Krummel, P. B., and Gerber, H.: Microphysical and radiative structure of wintertime marine stratocumulus clouds over the Southern Ocean, Q. J. Roy. Meteor. Soc., 122, 1307–1339, 1996.
Boers, R., Jensen, J. B., and Krummel, P. B.: Microphysical and shortwave radiative structure of stratocumulus clouds over the Southern Ocean: summer results and seasonal differences, Q. J. Roy. Meteor. Soc., 124, 151–168, 1998.
Boyd, P., LaRoche, J., Gall, M., Frew, R., and McKay, R. M. L.: Role of iron, light, and silicate in controlling algal biomass in subantarctic waters SE of New Zealand, J. Geophys. Res.-Oceans, 104, 13395–13408, https://doi.org/10.1029/1999jc900009, 1999.
Boyd, P. W., McTainsh, G., Sherlock, V., Richardson, K., Nichol, S., Ellwood, M., and Frew, R.: Episodic enhancement of phytoplankton stocks in New Zealand subantarctic waters: Contribution of atmospheric and oceanic iron supply, Global Biogeochem. Cy., 18, GB1029, https://doi.org/10.1029/2002GB002020, 2004.
Bradford-Grieve, J. M., Boyd, P. W., Chang, F. H., Chiswell, S., Hadfield, M., Hall, J. A., James, M. R., Nodder, S. D., and Shushkina, E. A.: Pelagic ecosystem structure and functioning in the Subtropical Front region east of New Zealand in austral winter and spring 1993, J. Plankton Res., 21, 405–428, https://doi.org/10.1093/plankt/21.3.405, 1999.
Cainey, J. and Harvey, M.: Dimethylsulfide, a limited contributor to new particle formation in the clean marine boundary layer, Geophys. Res. Lett., 29, 32-1–32-4, https://doi.org/10.1029/2001GL014439, 2002.
Calleja, M. L., Duarte, C. M., Navarro, N., and Agustí, S.: Control of air-sea CO2 disequilibria in the subtropical NE Atlantic by planktonic metabolism under the ocean skin, Geophys. Res. Lett., 32, L08606, https://doi.org/10.1029/2004GL022120, 2005.
Calleja, M. L., Duarte, C. M., Alvarez, M., Vaquer-Sunyer, R., Agusti, S., and Herndl, G. J.: Prevalence of strong vertical CO2 and O-2 variability in the top meters of the ocean, Global Biogeochem. Cy., 27, 941–949, https://doi.org/10.1002/gbc.20081, 2013.
Carslaw, K. S., Boucher, O., Spracklen, D. V., Mann, G. W., Rae, J. G. L., Woodward, S., and Kulmala, M.: A review of natural aerosol interactions and feedbacks within the Earth system, Atmos. Chem. Phys., 10, 1701–1737, https://doi.org/10.5194/acp-10-1701-2010, 2010.
Carslaw, K. S., Lee, L. A., Reddington, C. L., Pringle, K. J., Rap, A., Forster, P. M., Mann, G. W., Spracklen, D. V., Woodhouse, M. T., Regayre, L. A., and Pierce, J. R.: Large contribution of natural aerosols to uncertainty in indirect forcing, Nature, 503, 66–71, 2013.
Chang, F. H. and Gall, M.: Phytoplankton assemblages and photosynthetic pigments during winter and spring in the Subtropical Convergence region near New Zealand, New Zeal. J. Mar. Fresh., 32, 515–530, 1998.
Chang, R. Y. W., Sjostedt, S. J., Pierce, J. R., Papakyriakou, T. N., Scarratt, M. G., Michaud, S., Levasseur, M., Leaitch, W. R., and Abbatt, J. P.: Relating atmospheric and oceanic DMS levels to particle nucleation events in the Canadian Arctic, J. Geophys. Res.-Atmos., 116, D00S03, https://doi.org/10.1029/2011JD015926, 2011.
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.
Chiswell, S. M., Bradford-Grieve, J., Hadfield, M. G., and Kennan, S. C.: Climatology of surface chlorophyll a, autumn-winter and spring blooms in the southwest Pacific Ocean, J. Geophys. Re.-Oceans, 118, 1003–1018, https://doi.org/10.1002/jgrc.20088, 2013.
Ciuraru, R., Fine, L., Pinxteren, M. V., D'Anna, B., Herrmann, H., and George, C.: Unravelling new processes at interfaces: Photochemical isoprene production at the sea surface, Environ. Sci. Technol., 49, 13199–13205, 2015.
Clarke, A. D., Freitag, S., Simpson, R. M. C., Hudson, J. G., Howell, S. G., Brekhovskikh, V. L., Campos, T., Kapustin, V. N., and Zhou, J.: Free troposphere as a major source of CCN for the equatorial pacific boundary layer: long-range transport and teleconnections, Atmos. Chem. Phys., 13, 7511–7529, https://doi.org/10.5194/acp-13-7511-2013, 2013.
Cohen, D. D., Stelcer, E., Hawas, O., and Garton, D.: IBA methods for characterisation of fine particulate atmospheric pollution: a local, regional and global research problem, The 13th International Conference on Particle Induced X-ray Emission (PIXE 2013), 219–220, 145–152, 2004.
Cravigan, L. T., Ristovski, Z., Modini, R. L., Keywood, M. D., and Gras, J. L.: Observation of sea-salt fraction in sub-100 nm diameter particles at Cape Grim, J. Geophys. Res.-Atmos., 5, 2014JD022601, https://doi.org/10.1002/2014JD022601, 2015.
de Bruyn, W. J., Harvey, M., Cainey, J. M., and Saltzman, E. S.: DMS and SO2 at Baring Head, New Zealand: Implications for the yield of SO2 from DMS, J. Atmos. Chem., 41, 189–209, https://doi.org/10.1023/a:1014252106572, 2002.
Decesari, S., Finessi, E., Rinaldi, M., Paglione, M., Fuzzi, S., Stephanou, E. G., Tziaras, T., Spyros, A., Ceburnis, D., O'Dowd, C., and Dall'Osto, M.: Primary and secondary marine organic aerosols over the North Atlantic Ocean during the MAP experiment, J. Geophys. Res.-Atmos., 116, D22210, https://doi.org/10.1029/2011JD016204, 2011.
de Leeuw, G., Guieu, C., Arneth, A., Bellouin, N., Bopp, L., Boyd, P. W., van der Gon, H. A. C. D., Desboeufs, K. V., Dulac, F., Facchini, M. C., Gantt, B., Langmann, B., Mahowald, N. M., Maranön, E., O'Dowd, C., Olgun, N., Pulido-Villena, E., Rinaldi, M., Stephanou, E. G., and Wagener, T.: Ocean–Atmosphere Interactions of Particles, edited by: Liss, P. S. and Johnson, M. T., Ocean-Atmosphere Interactions of Gases and Particles, Springer Earth System Sciences, 171–246, https://doi.org/10.1007/978-3-642-25643-1_4, 2014.
Delizo, L., Smith, W. O., and Hall, J.: Taxonomic composition and growth rates of phytoplankton assemblages at the Subtropical Convergence east of New Zealand, J. Plankton Res., 29, 655–670, https://doi.org/10.1093/plankt/fbm047, 2007.
Draxler, R. R. and Rolph, G. D. (Eds.): HYSPLIT(HYbrid Single-PArticle Lagrangian Intergrated Trajectory) Model, NOAA Air Resources Laboratory, College Park, MD, available at: http://www.arl.noaa.gov/HYSPLIT.php, last access: 1 September 2013.
Facchini, M. C., Rinaldi, M., Decesari, S., Carbone, C., Finessi, E., Mircea, M., Fuzzi, S., Ceburnis, D., Flanagan, R., Nilsson, E. D., de Leeuw, G., Martino, M., Woeltjen, J., and O'Dowd, C. D.: Primary submicron marine aerosol dominated by insoluble organic colloids and aggregates, Geophys. Res. Lett., 35, L17814, https://doi.org/10.1029/2008GL034210, 2008.
Fairall, C. W., Bradley, E. F., Hare, J. E., Grachev, A. A., and Edson, J. B.: Bulk parameterization of air-sea fluxes: Updates and verification for the COARE algorithm, J. Climate, 16, 571–591, 2003.
Fairall, C. W., Yang, M. X., Bariteau, L., Edson, J. B., Helmig, D., McGillis, W., Pezoa, S., Hare, J. E., Huebert, B., and Blomquist, B.: Implementation of the Coupled Ocean-Atmosphere Response Experiment flux algorithm with CO2, dimethyl sulfide, and O-3, J. Geophys. Res.-Oceans, 116, C00F09, https://doi.org/10.1029/2010jc006884, 2011.
Gantt, B. and Meskhidze, N.: The physical and chemical characteristics of marine primary organic aerosol: a review, Atmos. Chem. Phys., 13, 3979–3996, https://doi.org/10.5194/acp-13-3979-2013, 2013.
Gantt, B., Meskhidze, N., Facchini, M. C., Rinaldi, M., Ceburnis, D., and O'Dowd, C. D.: Wind speed dependent size-resolved parameterization for the organic mass fraction of sea spray aerosol, Atmos. Chem. Phys., 11, 8777–8790, https://doi.org/10.5194/acp-11-8777-2011, 2011.
Gondwe, M., Krol, M., Gieskes, W., Klaassen, W., and De Baar, H.: The contribution of ocean-leaving DMS to the global atmospheric burdens of DMS, MSA, SO2, and NSS SO4−, Global Biogeochem. Cy., 17, 1056, https://doi.org/10.1029/2002GB001937, 2003.
Griffiths, F. B., Bates, T. S., Quinn, P. K., Clementson, L. A., and Parslow, J. S.: Oceanographic context of the First Aerosol Characterization Experiment (ACE 1): A physical, chemical, and biological overview, J. Geophys. Res.-Atmos., 104, 21649–21671, https://doi.org/10.1029/1999jd900386, 1999.
Harvey, M. J., Wylie, D. J., Martin, R. J., Clarkson, T. S., and de Mora, S. J.: Dimethylsulphide measurements at Baring Head, New Zealand, in: Dimethylsulphide, Oceans, Atmosphere and Climate, edited by: Restelli, G., and Angeletti, G., Kluwer Academic, Dordrecht, 143–151, 1993.
Harvey, M. J., Law, C. S., Smith, M. J., Hall, J. A., Abraham, E. R., Stevens, C. L., Hadfield, M. G., Ho, D. T., Ward, B., Archer, S. D., Cainey, J. M., Currie, K. I., Devries, D., Ellwood, M. J., Hill, P., Jones, G. B., Katz, D., Kuparinen, J., Macaskill, B., Main, W., Marriner, A., McGregor, J., McNeil, C., Minnett, P. J., Nodder, S. D., Peloquin, J., Pickmere, S., Pinkerton, M. H., Safi, K. A., Thompson, R., Walkington, M., Wright, S. W., and Ziolkowski, L. A.: The SOLAS air-sea gas exchange experiment (SAGE) 2004, Deep Sea Res. Pt. II, 58, 753–763, https://doi.org/10.1016/j.dsr2.2010.10.015, 2011.
Harvey, M. J., McGregor, J. A., Lawson, S. J., Cravigan, L., Talbot, N., Olivares, G., Conners, S., and Woodhouse, M.: Aerosol and tracer measurement at sea – defining the baseline, Atmos. Chem. Phys. Dicuss., in preparation, 2017.
Ho, D. T., Law, C. S., Smith, M. J., Schlosser, P., Harvey, M., and Hill, P.: Measurements of air-sea gas exchange at high wind speeds in the Southern Ocean: Implications for global parameterizations, Geophys. Res. Lett., 33, L16611, https://doi.org/10.1029/2006GL026817, 2006.
Jaeglé, L., Quinn, P. K., Bates, T. S., Alexander, B., and Lin, J.-T.: Global distribution of sea salt aerosols: new constraints from in situ and remote sensing observations, Atmos. Chem. Phys., 11, 3137–3157, https://doi.org/10.5194/acp-11-3137-2011, 2011.
Johnson, G., Ristovski, Z., and Morawska, L.: Application of the VH-TDMA technique to coastal ambient aerosols, Geophys. Res. Lett., 31, L16105, https://doi.org/10.1029/2004GL020126, 2004.
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.
Kay, J. E., Wall, C., Yettella, V., Medeiros, B., Hannay, C., Caldwell, P., and Bitz, C.: Global Climate Impacts of Fixing the Southern Ocean Shortwave Radiation Bias in the Community Earth System Model (CESM), J. Climate, 29, 4617–4636, https://doi.org/10.1175/JCLI-D-15-0358.1, 2016.
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.
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.
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.
Lana, A., Simó, R., Vallina, S. M., and Dachs, J.: Potential for a biogenic influence on cloud microphysics over the ocean: a correlation study with satellite-derived data, Atmos. Chem. Phys., 12, 7977–7993, https://doi.org/10.5194/acp-12-7977-2012, 2012.
Landschuetzer, P., Gruber, N., Bakker, D. C. E., and Schuster, U.: Recent variability of the global ocean carbon sink, Global Biogeochem. Cy., 28, 927–949, https://doi.org/10.1002/2014gb004853, 2014.
Landwehr, S., Miller, S. D., Smith, M. J., Saltzman, E. S., and Ward, B.: Analysis of the PKT correction for direct CO2 flux measurements over the ocean, Atmos. Chem. Phys., 14, 3361–3372, https://doi.org/10.5194/acp-14-3361-2014, 2014.
Landwehr, S., Miller, S. D., Smith, M. J., Saltzman, E. S., Bell, T. G., and Ward, B.: Using Eddy Covariance to Measure the Dependence of Air-Sea CO2 Exchange Rate on Friction Velocity, Atmos. Chem. Phys. Discuss, submitted, 2017.
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.
Lawson, S. J., Selleck, P. W., Cheng, M., and Harvey, M.: VOCs in marine air over the biologically productive Chatham Rise, Atmos. Chem. Phys. Discuss., in preparation, 2017.
Lizotte, M., Levasseur, M., Law, C. S., Walker, C. F., Safi, K. A., Marriner, A., and Kiene, R. P.: Dimethylsulfoniopropionate (DMSP) and dimethylsulfide (DMS) cycling across contrasting biological hotspots of the New Zealand Subtropical Front, Ocean Sci. Discuss., https://doi.org/10.5194/os-2017-32, in review, 2017.
Longhurst A. : Ecological Geography of the Sea, Acad. Press, London, 1998.
Mahajan, A. S., Prados-Roman, C., Hay, T. D., Lampel, J., Pöhler, D., Großmann, K., Tschritter, J., Frieß, U., Platt, U., Johnston, P., Kreher, K., Wittrock, F., Burrows, J. P., Plane, J. M. C., and Saiz-Lopez, A.: Glyoxal observations in the global marine boundary layer, J. Geophys. Res.-Atmos., 119, 6160–6169, https://doi.org/10.1002/2013JD021388, 2014.
Mahajan, A. S., Fadnavis, S., Thomas, M. A., Pozzoli, L., Gupta, S., Royer, S.-J., Saiz-Lopez, A., and Simó, 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.
Mallet, M., Cravigan, L., Miljevic, B., Vaattovaara, P., Deschaseaux, E., Swan, H., Jones, G., and Ristovski, Z.: Sea spray aerosol in the Great Barrier Reef and the presence of nonvolatile organics, J. Geophys. Res.-Atmos., 121, 7088–709, https://doi.org/10.1002/2016JD024966, 2016.
Mann, G. W., Carslaw, K. S., Spracklen, D. V., Ridley, D. A., Manktelow, P. T., Chipperfield, M. P., Pickering, S. J., and Johnson, C. E.: Description and evaluation of GLOMAP-mode: a modal global aerosol microphysics model for the UKCA composition-climate model, Geosci. Model Dev., 3, 519–551, https://doi.org/10.5194/gmd-3-519-2010, 2010.
Mann, G. W., Carslaw, K. S., Ridley, D. A., Spracklen, D. V., Pringle, K. J., Merikanto, J., Korhonen, H., Schwarz, J. P., Lee, L. A., Manktelow, P. T., Woodhouse, M. T., Schmidt, A., Breider, T. J., Emmerson, K. M., Reddington, C. L., Chipperfield, M. P., and Pickering, S. J.: Intercomparison of modal and sectional aerosol microphysics representations within the same 3-D global chemical transport model, Atmos. Chem. Phys., 12, 4449–4476, https://doi.org/10.5194/acp-12-4449-2012, 2012.
Marandino, C. A., De Bruyn, W. J., Miller, S. D., and Saltzman, E. S.: DMS air/sea flux and gas transfer coefficients from the North Atlantic summertime coccolithophore bloom, Geophys. Res. Lett., 35, L23812, https://doi.org/10.1029/2008gl036370, 2008.
McCoy, D. T., Burrows, S. M., Wood, R., Grosvenor, D. P., Elliott, S. M., Ma, P.-L., Rasch, P. J., and Hartmann, D. L.: Natural aerosols explain seasonal and spatial patterns of Southern Ocean cloud albedo, Sci. Adv., 1, e1500157, https://doi.org/10.1126/sciadv.1500157, 2015.
Meskhidze, N. and Nenes, A.: Phytoplankton and cloudiness in the Southern Ocean, Science, 314, 1419–1423, 2006.
Meskhidze, N. and Nenes, A.: Effects of Ocean Ecosystem on Marine Aerosol-Cloud Interaction, Adv. Meteorol., 2010, 239808, https://doi.org/10.1155/2010/239808, 2010.
Meskhidze, N., Xu, J., Zhang, Y., Gantt, B., Ghan, S., Nenes, A., Liu, X., Easter, R., and Zaveri, R.: Effect of marine biogenic organic aerosols on cloud properties: Modeling study, Geochim. Cosmochim. Ac., 73, p. A874, 2009.
Meskhidze, N., Xu, J., Gantt, B., Zhang, Y., Nenes, A., Ghan, S. J., Liu, X., Easter, R., and Zaveri, R.: Global distribution and climate forcing of marine organic aerosol: 1. Model improvements and evaluation, Atmos. Chem. Phys., 11, 11689–11705, https://doi.org/10.5194/acp-11-11689-2011, 2011.
Modini, R. L., Harris, B., and Ristovski, Z. D.: The organic fraction of bubble-generated, accumulation mode Sea Spray Aerosol (SSA), Atmos. Chem. Phys., 10, 2867–2877, https://doi.org/10.5194/acp-10-2867-2010, 2010.
Murphy, R. J., Pinkerton, M. H., Richardson, K. M., Bradford-Grieve, J. M., and Boyd, P. W.: Phytoplankton distributions around New Zealand derived from SeaWiFS remotely-sensed ocean colour data, New Zeal. J. Mar. Fresh., 35, 343–362, 2001.
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, 2000.
Nodder, S. D., Duineveld, G. C. A., Pilditch, C. A., Sutton, P. J., Probert, P. K., Lavaleye, M. S. S., Witbaard, R., Chang, F. H., Hall, J. A., and Richardson, K. M.: Focusing of phytodetritus deposition beneath a deep-ocean front, Chatham Rise, New Zealand, Limnol. Oceanogr., 52, 299–314, 2007.
O'Dowd, C., Monahan, C., and Dall'Osto, M.: On the occurrence of open ocean particle production and growth events, Geophys. Res. Lett., 37, L19805, https://doi.org/10.1029/2010gl044679, 2010.
O'Dowd, C. D. and de Leeuw, G.: Marine aerosol production: a review of the current knowledge, Philos. T. R. Soc. A., 365, 1753–1774, 2007.
O'Dowd, C. D., Facchini, M. C., Cavalli, F., Ceburnis, D., Mircea, M., Decesari, S., Fuzzi, S., Yoon, Y. J., and Putaud, J.-P.: Biogenically driven organic contribution to marine aerosol, Nature, 431, 676–680, 2004.
Popinet, S., Smith, M., and Stevens, C.: Experimental and Numerical Study of the Turbulence Characteristics of Airflow around a Research Vessel, J. Atmos. Ocean. Tech., 21, 1575–1589, https://doi.org/10.1175/1520-0426(2004)021<1575:EANSOT>2.0.CO;2, 2004.
Quinn, P. K. and Bates, T. S.: The case against climate regulation via oceanic phytoplankton sulphur emissions, Nature, 480, 51–56, 2011.
Quinn, P. K., Bates, T. S., Schulz, K. S., Coffman, D. J., Frossard, A. A., Russell, L. M., Keene, W. C., and Kieber, D. J.: Contribution of sea surface carbon pool to organic matter enrichment in sea spray aerosol, Nat. Geosci., 7, 228–232, 2014.
Rinaldi, M., Fuzzi, S., Decesari, S., Marullo, S., Santoleri, R., Provenzale, A., von Hardenberg, J., Ceburnis, D., Vaishya, A., O'Dowd, C. D., and Facchini, M. C.: Is chlorophyll-a the best surrogate for organic matter enrichment in submicron primary marine aerosol?, J. Geophys. Res.-Atmos., 118, 4964–4973, https://doi.org/10.1002/jgrd.50417, 2013.
Russell, L. M., Hawkins, L. N., Frossard, A. A., Quinn, P. K., and Bates, T. S.: Carbohydrate-like composition of submicron atmospheric particles and their production from ocean bubble bursting, P. Natl. Acad. Sci. USA, 107, 6652–6657, https://doi.org/10.1073/pnas.0908905107, 2010.
Russell, L. M., Bahadur, R., and Ziemann, P. J.: Identifying organic aerosol sources by comparing functional group composition in chamber and atmospheric particles, P. Natl. Acad. Sci. USA, 108.9, 3516–3521, 2011.
Sadeghi, A., Dinter, T., Vountas, M., Taylor, B. B., Altenburg-Soppa, M., Peeken, I., and Bracher, A.: Improvement to the PhytoDOAS method for identification of coccolithophores using hyper-spectral satellite data, Ocean Sci., 8, 1055–1070, https://doi.org/10.5194/os-8-1055-2012, 2012.
Scanlon, B. and Ward, B.: The influence of environmental parameters on active and maturing oceanic whitecaps, J. Geophys. Res.-Oceans, 121, 8:1–12, https://doi.org/10.1002/2015JC011230, 2016.
Seinfeld, J. H., Bretherton, C., Carslaw, K. S., Coe, H., DeMott, P. J., Dunlea, E. J., Feingold, G., Ghan, S., Guenther, A. B., Kahn, R., Kraucunas, I., Kreidenweis, S. M., Molina, M. J., Nenes, A., Penner, J. E., Prather, K. A., Ramanathan, V., Ramaswamy, V., Rasch, P. J., Ravishankara, A. R., Rosenfeld, D., Stephens, G., and Wood, R.: Improving our fundamental understanding of the role of aerosol−cloud interactions in the climate system, P. Natl. Acad. Sci. USA, 113, 5781–5790, https://doi.org/10.1073/pnas.1514043113, 2016.
Sellegri, K., Loon, Y. J., Jennings, S. G., O'Dowd, C. D., Pirjola, L., Cautenet, S., Chen, H. W., and Hoffmann, T.: Quantification of coastal new ultra-fine particles formation from in situ and chamber measurements during the BIOFLUX campaign, Environ. Chem., 2, 260–270, https://doi.org/10.1071/en05074, 2005.
Sievering, H., Cainey, J., Harvey, M., McGregor, J., Nichol, S., and Quinn, P.: Aerosol non-sea-salt sulfate in the remote marine boundary layer under clear-sky and normal cloudiness conditions: Ocean-derived biogenic alkalinity enhances sea-salt sulfate production by ozone oxidation, J. Geophys. Res.-Atmos., 109, D19317, https://doi.org/10.1029/2003jd004315, 2004.
Smith, M. J., Ho, D. T., Law, C. S., McGregor, J., Popinet, S., and Schlosser, P.: Uncertainties in gas exchange parameterization during the SAGE dual-tracer experiment, Deep-Sea Res. Pt. II, 58, 869–881, https://doi.org/10.1016/j.dsr2.2010.10.025, 2011.
Smith, M. J., Walker, C. F., Bell, T. G., Harvey, M. J., Law, C. S., and Saltzman, E. S.: Gradient flux measurements of sea-air DMS transfer during the Surface Ocean Aerosol Production (SOAP) experiment, Atmos. Chem. Phys. Discuss., submitted, 2017.
Spada, M., Jorba, O., Pérez García-Pando, C., Janjic, Z., and Baldasano, J. M.: On the evaluation of global sea-salt aerosol models at coastal/orographic sites, Atmos. Environ., 101, 41–48, https://doi.org/10.1016/j.atmosenv.2014.11.019, 2015.
Stephens, G. L.: Cloud feedbacks in the climate system: A critical review, J. Climate, 18, 237–273, 2005.
Stevens, C. L., Hill, P., Smith, M. J., and Popinet, S.: SUCA: An engine for repetitive autonomous profiling near the ocean surface, Limnol. Oceanogr.-Meth., 3, 300–307, 2005.
Swan, H. B., Armishaw, P., Lavetz, R., Alamgir, M., Davies, S. R., Bell, T. G., and Jones, G. B.: An interlaboratory comparison for the quantification of aqueous dimethylsulfide, Limnol. Oceanogr.-Meth., 12, 784–794, https://doi.org/10.4319/lom.2014.12.784, 2014.
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.
Trenberth, K. E. and Fasullo, J. T.: Simulation of present-day and twenty-first-century energy budgets of the southern oceans, J. Climate, 23, 440–454, 2010.
Twomey, S.: The influence of pollution on the shortwave albedo of clouds, J. Atmos. Sci., 34, 1149–1152, 1977.
Vaattovaara, P., Räsänen, M., Kühn, T., Joutsensaari, J., and Laaksonen, A.: A method for detecting the presence of organic fraction in nucleation mode sized particles, Atmos. Chem. Phys., 5, 3277–3287, https://doi.org/10.5194/acp-5-3277-2005, 2005.
Vaattovaara, P., Huttunen, P. E., Yoon, Y. J., Joutsensaari, J., Lehtinen, K. E. J., O'Dowd, C. D., and Laaksonen, A.: The composition of nucleation and Aitken modes particles during coastal nucleation events: evidence for marine secondary organic contribution, Atmos. Chem. Phys., 6, 4601–4616, https://doi.org/10.5194/acp-6-4601-2006, 2006.
Vaishya, A., Jennings, S. G., and O'Dowd, C.: Wind-driven influences on aerosol light scattering in north-east Atlantic air, Geophys. Res. Lett., 39, L05805, https://doi.org/10.1029/2011GL050556, 2012.
Vallina, S. M., Simó, R., and Gassó, S.: What controls CCN seasonality in the Southern Ocean? A statistical analysis based on satellite-derived chlorophyll and CCN and model-estimated OH radical and rainfall, Global Biogeochem. Cy., 20, GB1014, https://doi.org/10.1029/2005GB002597, 2006.
Vignati, E., Facchini, M. C., Rinaldi, M., Scannell, C., Ceburnis, D., Sciare, J., Kanakidou, M., Myriokefalitakis, S., Dentener, F., and O'Dowd, C. D.: Global scale emission and distribution of sea-spray aerosol: Sea-salt and organic enrichment, Atmos. Environ., 44, 670–677, 2010.
Villani, P., Picard, D., Michaud, V., Laj, P., and Wiedensohler, A.: Design and Validation of a Volatility Hygroscopic Tandem Differential Mobility Analyzer (VH-TDMA) to Characterize the Relationships Between the Thermal and Hygroscopic Properties of Atmospheric Aerosol Particles, Aerosol Sci. Technol., 42, 729–741, https://doi.org/10.1080/02786820802255668, 2008.
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.
Wang, H., Easter, R. C., Rasch, P. J., Wang, M., Liu, X., Ghan, S. J., Qian, Y., Yoon, J.-H., Ma, P.-L., and Vinoj, V.: Sensitivity of remote aerosol distributions to representation of cloud–aerosol interactions in a global climate model, Geosci. Model Dev., 6, 765–782, https://doi.org/10.5194/gmd-6-765-2013, 2013.
Willis, M. D., Burkart, J., Thomas, J. L., Köllner, F., Schneider, J., Bozem, H., Hoor, P. M., Aliabadi, A. A., Schulz, H., Herber, A. B., Leaitch, W. R., and Abbatt, J. P. D.: Growth of nucleation mode particles in the summertime Arctic: a case study, Atmos. Chem. Phys., 16, 7663–7679, https://doi.org/10.5194/acp-16-7663-2016, 2016.
Woodhouse, M. T., Luhar, A. K., Stevens, L., Galbally, I., Thatcher, M., Uhe, P., Wolff, H., Noonan, J., and Molloy, S.: Australian reactive-gas emissions in a global chemistry-climate model and initial results, Air Quality and Climate Change, 49, 31–38, 2015.
Wylie, D. J. and de Mora, S. J.: Atmospheric dimethylsulfide and sulfur species in aerosol and rainwater at coastal site in New Zealand, J. Geophys. Res., 101, 21041–21049, 1996.
Yang, M., Blomquist, B. W., Fairall, C. W., Archer, S. D., and Huebert, B. J.: Air-sea exchange of dimethylsulfide in the Southern Ocean: Measurements from SO GasEx compared to temperate and tropical regions, J. Geophys. Res., 116, C00F05, https://doi.org/10.1029/2010JC006526, 2011.
Young, I. R., Vinoth, J., Zieger, S., and Babanin, A. V.: Investigation of trends in extreme value wave height and wind speed, J. Geophys. Res.-Oceans, 117, C00J06, https://doi.org/10.1029/2011JC007753, 2012.
Zhang, R.: Getting to the Critical Nucleus of Aerosol Formation, Science, 328, 1366–1367, https://doi.org/10.1126/science.1189732, 2010.
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.
We carried out a multidisciplinary study to examine how aerosol production is influenced by the...
Altmetrics
Final-revised paper
Preprint