Airborne measurements of dimethylsulfide, sulfur dioxide, and aerosol ions over the Southern Ocean South of Australia
Vertical distributions of dimethylsulfide (DMS), sulfur dioxide (SO2), aerosol methane-sulfonate (MSA), non-sea-salt sulfate (nss-SO42-), and other aerosol ions were measured in maritime air west of Tasmania (Australia) during December 1986. A few cloudwater and rainwater samples were also collected...
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ftunivrhodeislan:oai:digitalcommons.uri.edu:gsofacpubs-2920 2024-02-04T10:04:42+01:00 Airborne measurements of dimethylsulfide, sulfur dioxide, and aerosol ions over the Southern Ocean South of Australia Berresheim, H. Andreae, M. O. Ayers, G. P. Gillett, R. W. Merrill, J. T. Davis, V. J. Chameides, W. L. 1990-04-01T08:00:00Z https://digitalcommons.uri.edu/gsofacpubs/1951 https://doi.org/10.1007/BF00053868 unknown DigitalCommons@URI https://digitalcommons.uri.edu/gsofacpubs/1951 doi:10.1007/BF00053868 https://doi.org/10.1007/BF00053868 Graduate School of Oceanography Faculty Publications dimethylsulfide marine aerosol Marine atmosphere methanesulfonate non-sea-salt sulfate Southern Ocean sulfur dioxide vertical distributions text 1990 ftunivrhodeislan https://doi.org/10.1007/BF00053868 2024-01-08T19:09:55Z Vertical distributions of dimethylsulfide (DMS), sulfur dioxide (SO2), aerosol methane-sulfonate (MSA), non-sea-salt sulfate (nss-SO42-), and other aerosol ions were measured in maritime air west of Tasmania (Australia) during December 1986. A few cloudwater and rainwater samples were also collected and analyzed for major anions and cations. DMS concentrations in the mixed layer (ML) were typically between 15-60 ppt (parts per trillion, 10-12; 24 ppt=1 nmol m-3 (20°C, 1013 hPa)) and decreased in the free troposphere (FT) to about <1-2.4 ppt at 3 km. One profile study showed elevated DMS concentrations at cloud level consistent with turbulent transport ('cloud pumping') of air below convective cloud cells. In another case, a diel variation of DMS was observed in the ML. Our data suggest that meteorological rather than photochemical processes were responsible for this behavior. Based on model calculations we estimate a DMS lifetime in the ML of 0.9 days and a DMS sea-to-air flux of 2-3 μmol m-2 d-1. These estimates pertain to early austral summer conditions and southern mid-ocean latitudes. Typical MSA concentrations were 11 ppt in the ML and 4.7-6.8 ppt in the FT. Sulfur-dioxide values were almost constant in the ML and the lower FT within a range of 4-22 ppt between individual flight days. A strong increase of the SO2 concentration in the middle FT (5.3 km) was observed. We estimate the residence time of SO2 in the ML to be about 1 day. Aqueous-phase oxidation in clouds is probably the major removal process for SO2. The corresponding removal rate is estimated to be a factor of 3 larger than the rate of homogeneous oxidation of SO2 by OH. Model calculations suggest that roughly two-thirds of DMS in the ML are converted to SO2 and one-third to MSA. On the other hand, MSA/nss-SO42- mole ratios were significantly higher compared to values previously reported for other ocean areas suggesting a relatively higher production of MSA from DMS oxidation over the Southern Ocean. Nss-SO42- profiles were mostly parallel to ... Text Southern Ocean University of Rhode Island: DigitalCommons@URI Austral Southern Ocean Journal of Atmospheric Chemistry 10 3 341 370 |
institution |
Open Polar |
collection |
University of Rhode Island: DigitalCommons@URI |
op_collection_id |
ftunivrhodeislan |
language |
unknown |
topic |
dimethylsulfide marine aerosol Marine atmosphere methanesulfonate non-sea-salt sulfate Southern Ocean sulfur dioxide vertical distributions |
spellingShingle |
dimethylsulfide marine aerosol Marine atmosphere methanesulfonate non-sea-salt sulfate Southern Ocean sulfur dioxide vertical distributions Berresheim, H. Andreae, M. O. Ayers, G. P. Gillett, R. W. Merrill, J. T. Davis, V. J. Chameides, W. L. Airborne measurements of dimethylsulfide, sulfur dioxide, and aerosol ions over the Southern Ocean South of Australia |
topic_facet |
dimethylsulfide marine aerosol Marine atmosphere methanesulfonate non-sea-salt sulfate Southern Ocean sulfur dioxide vertical distributions |
description |
Vertical distributions of dimethylsulfide (DMS), sulfur dioxide (SO2), aerosol methane-sulfonate (MSA), non-sea-salt sulfate (nss-SO42-), and other aerosol ions were measured in maritime air west of Tasmania (Australia) during December 1986. A few cloudwater and rainwater samples were also collected and analyzed for major anions and cations. DMS concentrations in the mixed layer (ML) were typically between 15-60 ppt (parts per trillion, 10-12; 24 ppt=1 nmol m-3 (20°C, 1013 hPa)) and decreased in the free troposphere (FT) to about <1-2.4 ppt at 3 km. One profile study showed elevated DMS concentrations at cloud level consistent with turbulent transport ('cloud pumping') of air below convective cloud cells. In another case, a diel variation of DMS was observed in the ML. Our data suggest that meteorological rather than photochemical processes were responsible for this behavior. Based on model calculations we estimate a DMS lifetime in the ML of 0.9 days and a DMS sea-to-air flux of 2-3 μmol m-2 d-1. These estimates pertain to early austral summer conditions and southern mid-ocean latitudes. Typical MSA concentrations were 11 ppt in the ML and 4.7-6.8 ppt in the FT. Sulfur-dioxide values were almost constant in the ML and the lower FT within a range of 4-22 ppt between individual flight days. A strong increase of the SO2 concentration in the middle FT (5.3 km) was observed. We estimate the residence time of SO2 in the ML to be about 1 day. Aqueous-phase oxidation in clouds is probably the major removal process for SO2. The corresponding removal rate is estimated to be a factor of 3 larger than the rate of homogeneous oxidation of SO2 by OH. Model calculations suggest that roughly two-thirds of DMS in the ML are converted to SO2 and one-third to MSA. On the other hand, MSA/nss-SO42- mole ratios were significantly higher compared to values previously reported for other ocean areas suggesting a relatively higher production of MSA from DMS oxidation over the Southern Ocean. Nss-SO42- profiles were mostly parallel to ... |
format |
Text |
author |
Berresheim, H. Andreae, M. O. Ayers, G. P. Gillett, R. W. Merrill, J. T. Davis, V. J. Chameides, W. L. |
author_facet |
Berresheim, H. Andreae, M. O. Ayers, G. P. Gillett, R. W. Merrill, J. T. Davis, V. J. Chameides, W. L. |
author_sort |
Berresheim, H. |
title |
Airborne measurements of dimethylsulfide, sulfur dioxide, and aerosol ions over the Southern Ocean South of Australia |
title_short |
Airborne measurements of dimethylsulfide, sulfur dioxide, and aerosol ions over the Southern Ocean South of Australia |
title_full |
Airborne measurements of dimethylsulfide, sulfur dioxide, and aerosol ions over the Southern Ocean South of Australia |
title_fullStr |
Airborne measurements of dimethylsulfide, sulfur dioxide, and aerosol ions over the Southern Ocean South of Australia |
title_full_unstemmed |
Airborne measurements of dimethylsulfide, sulfur dioxide, and aerosol ions over the Southern Ocean South of Australia |
title_sort |
airborne measurements of dimethylsulfide, sulfur dioxide, and aerosol ions over the southern ocean south of australia |
publisher |
DigitalCommons@URI |
publishDate |
1990 |
url |
https://digitalcommons.uri.edu/gsofacpubs/1951 https://doi.org/10.1007/BF00053868 |
geographic |
Austral Southern Ocean |
geographic_facet |
Austral Southern Ocean |
genre |
Southern Ocean |
genre_facet |
Southern Ocean |
op_source |
Graduate School of Oceanography Faculty Publications |
op_relation |
https://digitalcommons.uri.edu/gsofacpubs/1951 doi:10.1007/BF00053868 https://doi.org/10.1007/BF00053868 |
op_doi |
https://doi.org/10.1007/BF00053868 |
container_title |
Journal of Atmospheric Chemistry |
container_volume |
10 |
container_issue |
3 |
container_start_page |
341 |
op_container_end_page |
370 |
_version_ |
1789973340159475712 |