Measurements of particulate methanesulfonic acid above the remote Arctic Ocean using a high resolution aerosol mass spectrometer

9 pages, 6 figures, supplementary data https://doi.org/10.1016/j.atmosenv.2024.120538.-- Data availability: Data will be made available on request Methanesulfonic acid (MSA) is an important product from the oxidation of dimethyl sulfide (DMS), and thus is often used as a tracer for marine biogenic s...

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Published in:Atmospheric Environment
Main Authors: Zhang, Yangmei, Sun, Junying, Shen, Xiaojing, Chandani, Vipul Lal, Du, Mao, Song, Congbo, Dai, Yuqing, Hu, Guoyuan, Yang, Mingxi, Tilstone, Gavin H., Jordan, Tom, Dall'Olmo, Giorgio, Liu, Quan, Nemitz, Eiko, Callaghan, Anna, Brean, James, Sommariva, Roberto, Beddows, David C. S., Langford, Ben, Bloss, William J., Acton, William, Harrison, Roy M., Dall'Osto, Manuel, Shi, Zongbo
Other Authors: National Natural Science Foundation of China, Natural Environment Research Council (UK), European Space Agency, Agencia Estatal de Investigación (España)
Format: Article in Journal/Newspaper
Language:English
Published: Elsevier 2024
Subjects:
MSA
Online Access:http://hdl.handle.net/10261/366292
https://doi.org/10.1016/j.atmosenv.2024.120538
id ftcsic:oai:digital.csic.es:10261/366292
record_format openpolar
spelling ftcsic:oai:digital.csic.es:10261/366292 2024-09-15T17:54:20+00:00 Measurements of particulate methanesulfonic acid above the remote Arctic Ocean using a high resolution aerosol mass spectrometer Zhang, Yangmei Sun, Junying Shen, Xiaojing Chandani, Vipul Lal Du, Mao Song, Congbo Dai, Yuqing Hu, Guoyuan Yang, Mingxi Tilstone, Gavin H. Jordan, Tom Dall'Olmo, Giorgio Liu, Quan Nemitz, Eiko Callaghan, Anna Brean, James Sommariva, Roberto Beddows, David C. S. Langford, Ben Bloss, William J. Acton, William Harrison, Roy M. Dall'Osto, Manuel Shi, Zongbo National Natural Science Foundation of China Natural Environment Research Council (UK) European Space Agency Agencia Estatal de Investigación (España) 2024-08 http://hdl.handle.net/10261/366292 https://doi.org/10.1016/j.atmosenv.2024.120538 en eng Elsevier Postprint https://doi.org/10.1016/j.atmosenv.2024.120538 Sí Atmospheric Environment 331: 120538 (2024) 1352-2310 CEX2019-000928-S http://hdl.handle.net/10261/366292 doi:10.1016/j.atmosenv.2024.120538 1878-2442 embargo_20250831 MSA Marine aerosol Oxidation path Reference MSA/nss-SO4 value HR-ToF-AMS artículo 2024 ftcsic https://doi.org/10.1016/j.atmosenv.2024.120538 2024-09-02T14:08:53Z 9 pages, 6 figures, supplementary data https://doi.org/10.1016/j.atmosenv.2024.120538.-- Data availability: Data will be made available on request Methanesulfonic acid (MSA) is an important product from the oxidation of dimethyl sulfide (DMS), and thus is often used as a tracer for marine biogenic sources and secondary organic aerosol. MSA also contributes to aerosol mass and potentially to the formation of cloud condensation nuclei and new particles. However, measurements of MSA at high temporal resolution in the remote Arctic are scarce, which limits our understanding of its formation, climate change impact and regional transport. Here, we applied a validated quantification method to determine the mass concentration of MSA and non-sea salt sulfate (nss-SO4) in PM2.5 in the marine boundary layer, using a high resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS) during a research cruise to the Arctic and North Atlantic Ocean, between 55 °N and 68 °N (26th May to June 23, 2022). With this method, the concentrations of MSA in the remote Arctic marine boundary layer were determined for the first time. Results show that the average MSA concentration was 0.025 ± 0.03 μg m−3, ranging from <0.01 to 0.32 μg m−3. The lowest MSA level was found towards the northern leg of the cruise (near Sisimut (67 °N)) with air masses from sea ice over the northern polar region, and the highest MSA concentrations were observed over the Atlantic open ocean. The diurnal cycles of gas MSA, particulate MSA and nss-SO4 peaked in the afternoon, about one hour later than that of peak of solar radiation, which suggests that photochemical process is an important mechanism for the conversion of DMS into MSA above the remote ocean. The mass ratio of MSA to nss-SO4 (MSA/nss-SO4) presents a temperature dependence, which indicates that the addition branching pathway favors MSA formation, while thermal decay of intermediate radicals could be a possible pathway for sulfate formation. Finally, we found that the MSA/nss-SO4 ratio is ... Article in Journal/Newspaper Arctic Ocean Climate change North Atlantic Sea ice Digital.CSIC (Spanish National Research Council) Atmospheric Environment 331 120538
institution Open Polar
collection Digital.CSIC (Spanish National Research Council)
op_collection_id ftcsic
language English
topic MSA
Marine aerosol
Oxidation path
Reference MSA/nss-SO4 value
HR-ToF-AMS
spellingShingle MSA
Marine aerosol
Oxidation path
Reference MSA/nss-SO4 value
HR-ToF-AMS
Zhang, Yangmei
Sun, Junying
Shen, Xiaojing
Chandani, Vipul Lal
Du, Mao
Song, Congbo
Dai, Yuqing
Hu, Guoyuan
Yang, Mingxi
Tilstone, Gavin H.
Jordan, Tom
Dall'Olmo, Giorgio
Liu, Quan
Nemitz, Eiko
Callaghan, Anna
Brean, James
Sommariva, Roberto
Beddows, David C. S.
Langford, Ben
Bloss, William J.
Acton, William
Harrison, Roy M.
Dall'Osto, Manuel
Shi, Zongbo
Measurements of particulate methanesulfonic acid above the remote Arctic Ocean using a high resolution aerosol mass spectrometer
topic_facet MSA
Marine aerosol
Oxidation path
Reference MSA/nss-SO4 value
HR-ToF-AMS
description 9 pages, 6 figures, supplementary data https://doi.org/10.1016/j.atmosenv.2024.120538.-- Data availability: Data will be made available on request Methanesulfonic acid (MSA) is an important product from the oxidation of dimethyl sulfide (DMS), and thus is often used as a tracer for marine biogenic sources and secondary organic aerosol. MSA also contributes to aerosol mass and potentially to the formation of cloud condensation nuclei and new particles. However, measurements of MSA at high temporal resolution in the remote Arctic are scarce, which limits our understanding of its formation, climate change impact and regional transport. Here, we applied a validated quantification method to determine the mass concentration of MSA and non-sea salt sulfate (nss-SO4) in PM2.5 in the marine boundary layer, using a high resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS) during a research cruise to the Arctic and North Atlantic Ocean, between 55 °N and 68 °N (26th May to June 23, 2022). With this method, the concentrations of MSA in the remote Arctic marine boundary layer were determined for the first time. Results show that the average MSA concentration was 0.025 ± 0.03 μg m−3, ranging from <0.01 to 0.32 μg m−3. The lowest MSA level was found towards the northern leg of the cruise (near Sisimut (67 °N)) with air masses from sea ice over the northern polar region, and the highest MSA concentrations were observed over the Atlantic open ocean. The diurnal cycles of gas MSA, particulate MSA and nss-SO4 peaked in the afternoon, about one hour later than that of peak of solar radiation, which suggests that photochemical process is an important mechanism for the conversion of DMS into MSA above the remote ocean. The mass ratio of MSA to nss-SO4 (MSA/nss-SO4) presents a temperature dependence, which indicates that the addition branching pathway favors MSA formation, while thermal decay of intermediate radicals could be a possible pathway for sulfate formation. Finally, we found that the MSA/nss-SO4 ratio is ...
author2 National Natural Science Foundation of China
Natural Environment Research Council (UK)
European Space Agency
Agencia Estatal de Investigación (España)
format Article in Journal/Newspaper
author Zhang, Yangmei
Sun, Junying
Shen, Xiaojing
Chandani, Vipul Lal
Du, Mao
Song, Congbo
Dai, Yuqing
Hu, Guoyuan
Yang, Mingxi
Tilstone, Gavin H.
Jordan, Tom
Dall'Olmo, Giorgio
Liu, Quan
Nemitz, Eiko
Callaghan, Anna
Brean, James
Sommariva, Roberto
Beddows, David C. S.
Langford, Ben
Bloss, William J.
Acton, William
Harrison, Roy M.
Dall'Osto, Manuel
Shi, Zongbo
author_facet Zhang, Yangmei
Sun, Junying
Shen, Xiaojing
Chandani, Vipul Lal
Du, Mao
Song, Congbo
Dai, Yuqing
Hu, Guoyuan
Yang, Mingxi
Tilstone, Gavin H.
Jordan, Tom
Dall'Olmo, Giorgio
Liu, Quan
Nemitz, Eiko
Callaghan, Anna
Brean, James
Sommariva, Roberto
Beddows, David C. S.
Langford, Ben
Bloss, William J.
Acton, William
Harrison, Roy M.
Dall'Osto, Manuel
Shi, Zongbo
author_sort Zhang, Yangmei
title Measurements of particulate methanesulfonic acid above the remote Arctic Ocean using a high resolution aerosol mass spectrometer
title_short Measurements of particulate methanesulfonic acid above the remote Arctic Ocean using a high resolution aerosol mass spectrometer
title_full Measurements of particulate methanesulfonic acid above the remote Arctic Ocean using a high resolution aerosol mass spectrometer
title_fullStr Measurements of particulate methanesulfonic acid above the remote Arctic Ocean using a high resolution aerosol mass spectrometer
title_full_unstemmed Measurements of particulate methanesulfonic acid above the remote Arctic Ocean using a high resolution aerosol mass spectrometer
title_sort measurements of particulate methanesulfonic acid above the remote arctic ocean using a high resolution aerosol mass spectrometer
publisher Elsevier
publishDate 2024
url http://hdl.handle.net/10261/366292
https://doi.org/10.1016/j.atmosenv.2024.120538
genre Arctic Ocean
Climate change
North Atlantic
Sea ice
genre_facet Arctic Ocean
Climate change
North Atlantic
Sea ice
op_relation Postprint
https://doi.org/10.1016/j.atmosenv.2024.120538

Atmospheric Environment 331: 120538 (2024)
1352-2310
CEX2019-000928-S
http://hdl.handle.net/10261/366292
doi:10.1016/j.atmosenv.2024.120538
1878-2442
op_rights embargo_20250831
op_doi https://doi.org/10.1016/j.atmosenv.2024.120538
container_title Atmospheric Environment
container_volume 331
container_start_page 120538
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