Low contributions of dimethyl sulfide (DMS) chemistry to atmospheric aerosols over the high Arctic Ocean

The Arctic Ocean is continuously warming, resulting in sea ice retreat, which significantly impacts the marine biogenic sulfur cycle. The formation of aerosols from DMS oxidation and their climatic effects in the polar regions are of great concern. However, the impact of DMS chemistry on atmospheric...

Full description

Bibliographic Details
Main Authors: Zhang, Miming, Yan, Jinpei, Lin, Qi, Zheng, Hongguo, Park, Keyhong, Zhao, Shuhui, Xu, Suqing, Ruan, Meina, Wang, Shanshan, Zhong, Xinlin, Zhao, Suli
Format: Text
Language:English
Published: 2022
Subjects:
Online Access:https://doi.org/10.5194/acp-2022-454
https://acp.copernicus.org/preprints/acp-2022-454/
id ftcopernicus:oai:publications.copernicus.org:acpd104790
record_format openpolar
spelling ftcopernicus:oai:publications.copernicus.org:acpd104790 2023-05-15T14:51:11+02:00 Low contributions of dimethyl sulfide (DMS) chemistry to atmospheric aerosols over the high Arctic Ocean Zhang, Miming Yan, Jinpei Lin, Qi Zheng, Hongguo Park, Keyhong Zhao, Shuhui Xu, Suqing Ruan, Meina Wang, Shanshan Zhong, Xinlin Zhao, Suli 2022-07-18 application/pdf https://doi.org/10.5194/acp-2022-454 https://acp.copernicus.org/preprints/acp-2022-454/ eng eng doi:10.5194/acp-2022-454 https://acp.copernicus.org/preprints/acp-2022-454/ eISSN: 1680-7324 Text 2022 ftcopernicus https://doi.org/10.5194/acp-2022-454 2022-07-25T16:22:42Z The Arctic Ocean is continuously warming, resulting in sea ice retreat, which significantly impacts the marine biogenic sulfur cycle. The formation of aerosols from DMS oxidation and their climatic effects in the polar regions are of great concern. However, the impact of DMS chemistry on atmospheric aerosols in the high Arctic Ocean (AO) is still unclear due to the limitation of field observations and datasets. Gaseous methanesulfonic acid (MSA) and aerosol chemical species (MSA, SO 4 2- and DMA, etc.) were determined simultaneously with a high time resolution (1 hour) in the AO and Pacific Ocean (PO) to reveal the DMS chemistry in these regions. Extremely low MSA concentrations were observed in the high AO (75°–85° N), with an average of only 7.42 ± 6.60 ng•m -3 . However, high MSA concentrations, with an average of 168.60 ± 167.60 ng•m -3 were observed in the mid-latitude regions (45°–60° N). Sea salt aerosols were the most dominant source in the high Arctic Ocean, accounting for 88.78 % of the total aerosols, which was much larger than the values in the other regions. The MSA fraction was much lower in the high latitude regions than in the other regions, accounting for only 1.61 % of the total aerosol particles. The latitudinal distribution of MSA was consistent with that of DMS over the AO. Low DMS chemistry was determined based on the low DMS emissions in the HL region. These results highlight the contribution of DMS chemistry to atmospheric aerosols and extend the knowledge of how biogenic aerosols impact the regional atmosphere in the high AO. Text Arctic Arctic Ocean Sea ice Copernicus Publications: E-Journals Arctic Arctic Ocean Pacific
institution Open Polar
collection Copernicus Publications: E-Journals
op_collection_id ftcopernicus
language English
description The Arctic Ocean is continuously warming, resulting in sea ice retreat, which significantly impacts the marine biogenic sulfur cycle. The formation of aerosols from DMS oxidation and their climatic effects in the polar regions are of great concern. However, the impact of DMS chemistry on atmospheric aerosols in the high Arctic Ocean (AO) is still unclear due to the limitation of field observations and datasets. Gaseous methanesulfonic acid (MSA) and aerosol chemical species (MSA, SO 4 2- and DMA, etc.) were determined simultaneously with a high time resolution (1 hour) in the AO and Pacific Ocean (PO) to reveal the DMS chemistry in these regions. Extremely low MSA concentrations were observed in the high AO (75°–85° N), with an average of only 7.42 ± 6.60 ng•m -3 . However, high MSA concentrations, with an average of 168.60 ± 167.60 ng•m -3 were observed in the mid-latitude regions (45°–60° N). Sea salt aerosols were the most dominant source in the high Arctic Ocean, accounting for 88.78 % of the total aerosols, which was much larger than the values in the other regions. The MSA fraction was much lower in the high latitude regions than in the other regions, accounting for only 1.61 % of the total aerosol particles. The latitudinal distribution of MSA was consistent with that of DMS over the AO. Low DMS chemistry was determined based on the low DMS emissions in the HL region. These results highlight the contribution of DMS chemistry to atmospheric aerosols and extend the knowledge of how biogenic aerosols impact the regional atmosphere in the high AO.
format Text
author Zhang, Miming
Yan, Jinpei
Lin, Qi
Zheng, Hongguo
Park, Keyhong
Zhao, Shuhui
Xu, Suqing
Ruan, Meina
Wang, Shanshan
Zhong, Xinlin
Zhao, Suli
spellingShingle Zhang, Miming
Yan, Jinpei
Lin, Qi
Zheng, Hongguo
Park, Keyhong
Zhao, Shuhui
Xu, Suqing
Ruan, Meina
Wang, Shanshan
Zhong, Xinlin
Zhao, Suli
Low contributions of dimethyl sulfide (DMS) chemistry to atmospheric aerosols over the high Arctic Ocean
author_facet Zhang, Miming
Yan, Jinpei
Lin, Qi
Zheng, Hongguo
Park, Keyhong
Zhao, Shuhui
Xu, Suqing
Ruan, Meina
Wang, Shanshan
Zhong, Xinlin
Zhao, Suli
author_sort Zhang, Miming
title Low contributions of dimethyl sulfide (DMS) chemistry to atmospheric aerosols over the high Arctic Ocean
title_short Low contributions of dimethyl sulfide (DMS) chemistry to atmospheric aerosols over the high Arctic Ocean
title_full Low contributions of dimethyl sulfide (DMS) chemistry to atmospheric aerosols over the high Arctic Ocean
title_fullStr Low contributions of dimethyl sulfide (DMS) chemistry to atmospheric aerosols over the high Arctic Ocean
title_full_unstemmed Low contributions of dimethyl sulfide (DMS) chemistry to atmospheric aerosols over the high Arctic Ocean
title_sort low contributions of dimethyl sulfide (dms) chemistry to atmospheric aerosols over the high arctic ocean
publishDate 2022
url https://doi.org/10.5194/acp-2022-454
https://acp.copernicus.org/preprints/acp-2022-454/
geographic Arctic
Arctic Ocean
Pacific
geographic_facet Arctic
Arctic Ocean
Pacific
genre Arctic
Arctic Ocean
Sea ice
genre_facet Arctic
Arctic Ocean
Sea ice
op_source eISSN: 1680-7324
op_relation doi:10.5194/acp-2022-454
https://acp.copernicus.org/preprints/acp-2022-454/
op_doi https://doi.org/10.5194/acp-2022-454
_version_ 1766322240557678592