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DMS sea-to-air fluxes and their influence on sulfate aerosols over the Southern Ocean, south-east Indian Ocean and north-west Pacific Ocean

Cited 1 time in wos
Cited 1 time in scopus

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dc.contributor.authorZhang, Miming-
dc.contributor.authorMarandino, Christa A.-
dc.contributor.authorYan, Jinpei-
dc.contributor.authorLin, Qi-
dc.contributor.authorPark, Keyhong-
dc.contributor.authorXu, Guojie-
dc.date.accessioned2022-03-14T07:17:16Z-
dc.date.available2022-03-14T07:17:16Z-
dc.date.issued2021-04-
dc.identifier.urihttps://repository.kopri.re.kr/handle/201206/13266-
dc.description.abstractEnvironmental context The ocean-produced dimethyl sulfide (DMS) molecule is thought to affect cloud formation and the solar radiation budget at the Earth's surface, hence playing an important role in regulating climate. In this study, we calculated the DMS sea-to-air flux across the Southern Ocean, south-east Indian Ocean and north-west Pacific Ocean, and analysed the influence of DMS fluxes on sulfate aerosols. These results improved our understanding of the effects of DMS emissions on sulfate compounds in the atmosphere over the global ocean. Oceanic dimethyl sulfide (DMS) is the most abundant biogenic sulfur compound emitted into the atmosphere and could indirectly regulate the global climate by impacting end product sulfate aerosols. DMS emissions and their influence on sulfate aerosols, i.e. methanesulfonic acid (MSA) and non-sea-salt sulfate (nss-SO42-), were investigated over the Atlantic Ocean and Indian Ocean sectors of the Southern Ocean (SO), the south-east Indian Ocean, and the north-west Pacific Ocean from February to April 2014 during the 30th Chinese National Antarctic Research Expedition. We found a strong large-scale DMS source in the marginal sea ice zone from 34 degrees W to 14 degrees E of the SO (south of 60 degrees S), in which the mean flux was 49.0 +/- 65.6 mu mol m(-2) d(-1) (0.6-308.3 mu mol m(-2) d(-1), n = 424). We also found a second large-scale DMS source in the South Subtropical Front (similar to 40 degrees S, up to 50.8 mu mol m(-2) d(-1)). An inconsistency between concentrations of atmospheric sulfate compounds and DMS emissions along the cruise track was observed. The horizontal advection of air masses was likely the main reason for this discrepancy. Finally, the biological exposure calculation results also indicated that it is very difficult to observe a straightforward relationship between oceanic biomass and atmospheric MSA.en_US
dc.languageEnglishen_US
dc.language.isoenen_US
dc.subjectChemistryen_US
dc.subjectEnvironmental Sciences & Ecologyen_US
dc.subject.classification해당사항없음en_US
dc.titleDMS sea-to-air fluxes and their influence on sulfate aerosols over the Southern Ocean, south-east Indian Ocean and north-west Pacific Oceanen_US
dc.title.alternative남극해, 남동인도양 및 북서태평양에서 황에어로졸에 DMS의 플럭스가 미치는 영향 연구en_US
dc.typeArticleen_US
dc.identifier.bibliographicCitationZhang, Miming, et al. 2021. "DMS sea-to-air fluxes and their influence on sulfate aerosols over the Southern Ocean, south-east Indian Ocean and north-west Pacific Ocean". <em>ENVIRONMENTAL CHEMISTRY</em>, 18(5-6): 193-201.-
dc.citation.titleENVIRONMENTAL CHEMISTRYen_US
dc.citation.volume18en_US
dc.citation.number5-6en_US
dc.identifier.doi10.1071/EN21003-
dc.citation.startPage193en_US
dc.citation.endPage201en_US
dc.description.articleClassificationSCIE-
dc.description.jcrRateJCR 2019:59.302en_US
dc.subject.keyworddimethyl sulfideen_US
dc.subject.keywordDMSen_US
dc.subject.keywordsulfate aerosolen_US
dc.subject.keywordDMS sea-to-air fluxesen_US
dc.subject.keywordthe Southern Oceanen_US
dc.subject.keywordIndian Oceanen_US
dc.subject.keywordPacific Oceanen_US
dc.subject.keywordrelationshipsen_US
dc.identifier.localId2021-0408-
dc.identifier.scopusid2-s2.0-85105273113-
dc.identifier.wosid000645604700001-
Appears in Collections  
2021-2021, Carbon cycle change and ecosystem response under the Southern Ocean warming (21-21) / Park, Jisoo (PE21110)
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