TY - JOUR
T1 - Measurements of particulate methanesulfonic acid above the remote Arctic Ocean using a high resolution aerosol mass spectrometer
AU - Zhang, Yangmei
AU - Sun, Junying
AU - Shen, Xiaojing
AU - Lal Chandani, Vipul
AU - Du, Mao
AU - Song, Congbo
AU - Dai, Yuqing
AU - Hu, Guoyuan
AU - Yang, Mingxi
AU - Tilstone, Gavin H.
AU - Jordan, Tom
AU - Dall'Olmo, Giorgio
AU - Liu, Quan
AU - Nemitz, Eiko
AU - Callaghan, Anna
AU - Brean, James
AU - Sommariva, Roberto
AU - Beddows, David
AU - Langford, Ben
AU - Bloss, William
AU - Acton, William
AU - Shi, Zongbo
N1 - Publisher Copyright:
© 2024
PY - 2024/8/15
Y1 - 2024/8/15
N2 - 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 around 0.22-0.25 in the remote northern marine atmosphere.
AB - 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 around 0.22-0.25 in the remote northern marine atmosphere.
KW - HR-ToF-AMS
KW - Marine aerosol
KW - MSA
KW - Oxidation path
KW - Reference MSA/nss-SO value
UR - http://www.scopus.com/inward/record.url?scp=85193926095&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/937ba36f-26e3-3235-a09e-75bf665be061/
U2 - 10.1016/j.atmosenv.2024.120538
DO - 10.1016/j.atmosenv.2024.120538
M3 - Article
AN - SCOPUS:85193926095
SN - 1352-2310
VL - 331
JO - Atmospheric Environment
JF - Atmospheric Environment
M1 - 120538
ER -