Observational evidence for the formation of DMS-derived aerosols during Arctic phytoplankton blooms

The connection between marine biogenic dimethyl sulfide (DMS) and the formation of aerosol particles in the Arctic atmosphere was evaluated by analyzing atmospheric DMS mixing ratio, aerosol particle size distribution and aerosol chemical composition data that were concurrently collected at Ny-Ålesu...

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Published in:Atmospheric Chemistry and Physics
Main Authors: Park, Ki-Tae, Jang, Sehyun, Lee, Kitack, Yoon, Young Jun, Kim, Min-Seob, Park, Kihong, Cho, Hee-Joo, Kang, Jung-Ho, Udisti, Roberto, Lee, Bang-Yong, Shin, Kyung-Hoon
Format: Text
Language:English
Published: 2018
Subjects:
Online Access:https://doi.org/10.5194/acp-17-9665-2017
https://www.atmos-chem-phys.net/17/9665/2017/
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spelling ftcopernicus:oai:publications.copernicus.org:acp56555 2023-05-15T14:41:58+02:00 Observational evidence for the formation of DMS-derived aerosols during Arctic phytoplankton blooms Park, Ki-Tae Jang, Sehyun Lee, Kitack Yoon, Young Jun Kim, Min-Seob Park, Kihong Cho, Hee-Joo Kang, Jung-Ho Udisti, Roberto Lee, Bang-Yong Shin, Kyung-Hoon 2018-09-21 application/pdf https://doi.org/10.5194/acp-17-9665-2017 https://www.atmos-chem-phys.net/17/9665/2017/ eng eng doi:10.5194/acp-17-9665-2017 https://www.atmos-chem-phys.net/17/9665/2017/ eISSN: 1680-7324 Text 2018 ftcopernicus https://doi.org/10.5194/acp-17-9665-2017 2019-12-24T09:51:14Z The connection between marine biogenic dimethyl sulfide (DMS) and the formation of aerosol particles in the Arctic atmosphere was evaluated by analyzing atmospheric DMS mixing ratio, aerosol particle size distribution and aerosol chemical composition data that were concurrently collected at Ny-Ålesund, Svalbard (78.5° N, 11.8° E), during April and May 2015. Measurements of aerosol sulfur (S) compounds showed distinct patterns during periods of Arctic haze (April) and phytoplankton blooms (May). Specifically, during the phytoplankton bloom period the contribution of DMS-derived SO 4 2− to the total aerosol SO 4 2− increased by 7-fold compared with that during the proceeding Arctic haze period, and accounted for up to 70 % of fine SO 4 2− particles (< 2.5 µm in diameter). The results also showed that the formation of submicron SO 4 2− aerosols was significantly associated with an increase in the atmospheric DMS mixing ratio. More importantly, two independent estimates of the formation of DMS-derived SO 4 2− aerosols, calculated using the stable S-isotope ratio and the non-sea-salt SO 4 2− ∕ methanesulfonic acid ratio, respectively, were in close agreement, providing compelling evidence that the contribution of biogenic DMS to the formation of aerosol particles was substantial during the Arctic phytoplankton bloom period. Text Arctic Ny Ålesund Ny-Ålesund Phytoplankton Svalbard Copernicus Publications: E-Journals Arctic Ny-Ålesund Svalbard Atmospheric Chemistry and Physics 17 15 9665 9675
institution Open Polar
collection Copernicus Publications: E-Journals
op_collection_id ftcopernicus
language English
description The connection between marine biogenic dimethyl sulfide (DMS) and the formation of aerosol particles in the Arctic atmosphere was evaluated by analyzing atmospheric DMS mixing ratio, aerosol particle size distribution and aerosol chemical composition data that were concurrently collected at Ny-Ålesund, Svalbard (78.5° N, 11.8° E), during April and May 2015. Measurements of aerosol sulfur (S) compounds showed distinct patterns during periods of Arctic haze (April) and phytoplankton blooms (May). Specifically, during the phytoplankton bloom period the contribution of DMS-derived SO 4 2− to the total aerosol SO 4 2− increased by 7-fold compared with that during the proceeding Arctic haze period, and accounted for up to 70 % of fine SO 4 2− particles (< 2.5 µm in diameter). The results also showed that the formation of submicron SO 4 2− aerosols was significantly associated with an increase in the atmospheric DMS mixing ratio. More importantly, two independent estimates of the formation of DMS-derived SO 4 2− aerosols, calculated using the stable S-isotope ratio and the non-sea-salt SO 4 2− ∕ methanesulfonic acid ratio, respectively, were in close agreement, providing compelling evidence that the contribution of biogenic DMS to the formation of aerosol particles was substantial during the Arctic phytoplankton bloom period.
format Text
author Park, Ki-Tae
Jang, Sehyun
Lee, Kitack
Yoon, Young Jun
Kim, Min-Seob
Park, Kihong
Cho, Hee-Joo
Kang, Jung-Ho
Udisti, Roberto
Lee, Bang-Yong
Shin, Kyung-Hoon
spellingShingle Park, Ki-Tae
Jang, Sehyun
Lee, Kitack
Yoon, Young Jun
Kim, Min-Seob
Park, Kihong
Cho, Hee-Joo
Kang, Jung-Ho
Udisti, Roberto
Lee, Bang-Yong
Shin, Kyung-Hoon
Observational evidence for the formation of DMS-derived aerosols during Arctic phytoplankton blooms
author_facet Park, Ki-Tae
Jang, Sehyun
Lee, Kitack
Yoon, Young Jun
Kim, Min-Seob
Park, Kihong
Cho, Hee-Joo
Kang, Jung-Ho
Udisti, Roberto
Lee, Bang-Yong
Shin, Kyung-Hoon
author_sort Park, Ki-Tae
title Observational evidence for the formation of DMS-derived aerosols during Arctic phytoplankton blooms
title_short Observational evidence for the formation of DMS-derived aerosols during Arctic phytoplankton blooms
title_full Observational evidence for the formation of DMS-derived aerosols during Arctic phytoplankton blooms
title_fullStr Observational evidence for the formation of DMS-derived aerosols during Arctic phytoplankton blooms
title_full_unstemmed Observational evidence for the formation of DMS-derived aerosols during Arctic phytoplankton blooms
title_sort observational evidence for the formation of dms-derived aerosols during arctic phytoplankton blooms
publishDate 2018
url https://doi.org/10.5194/acp-17-9665-2017
https://www.atmos-chem-phys.net/17/9665/2017/
geographic Arctic
Ny-Ålesund
Svalbard
geographic_facet Arctic
Ny-Ålesund
Svalbard
genre Arctic
Ny Ålesund
Ny-Ålesund
Phytoplankton
Svalbard
genre_facet Arctic
Ny Ålesund
Ny-Ålesund
Phytoplankton
Svalbard
op_source eISSN: 1680-7324
op_relation doi:10.5194/acp-17-9665-2017
https://www.atmos-chem-phys.net/17/9665/2017/
op_doi https://doi.org/10.5194/acp-17-9665-2017
container_title Atmospheric Chemistry and Physics
container_volume 17
container_issue 15
container_start_page 9665
op_container_end_page 9675
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