Gradient flux measurements of sea–air DMS transfer during the Surface Ocean Aerosol Production (SOAP) experiment

Direct measurements of marine dimethylsulfide (DMS) fluxes are sparse, particularly in the Southern Ocean. The Surface Ocean Aerosol Production (SOAP) voyage in February–March 2012 examined the distribution and flux of DMS in a biologically active frontal system in the southwest Pacific Ocean. Th...

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Main Authors: M. J. Smith, C. F. Walker, T. G. Bell, M. J. Harvey, E. S. Saltzman, C. S. Law
Format: Article
Language:English
Published: Copernicus Publications 2018-04-01
Series:Atmospheric Chemistry and Physics
Online Access:https://www.atmos-chem-phys.net/18/5861/2018/acp-18-5861-2018.pdf
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spelling doaj-5ac61dd7e9c24e2f8aa4c7dcb40489992020-11-24T20:40:28ZengCopernicus PublicationsAtmospheric Chemistry and Physics1680-73161680-73242018-04-01185861587710.5194/acp-18-5861-2018Gradient flux measurements of sea–air DMS transfer during the Surface Ocean Aerosol Production (SOAP) experimentM. J. Smith0C. F. Walker1T. G. Bell2T. G. Bell3M. J. Harvey4E. S. Saltzman5C. S. Law6C. S. Law7National Institute of Water and Atmospheric Research (NIWA), Wellington, 6241, New ZealandNational Institute of Water and Atmospheric Research (NIWA), Wellington, 6241, New ZealandEarth System Science, University of California, Irvine, California, USAPlymouth Marine Laboratory, Plymouth, PL1 3DH, UKNational Institute of Water and Atmospheric Research (NIWA), Wellington, 6241, New ZealandEarth System Science, University of California, Irvine, California, USANational Institute of Water and Atmospheric Research (NIWA), Wellington, 6241, New ZealandDepartment of Chemistry, University of Otago, Dunedin, New ZealandDirect measurements of marine dimethylsulfide (DMS) fluxes are sparse, particularly in the Southern Ocean. The Surface Ocean Aerosol Production (SOAP) voyage in February–March 2012 examined the distribution and flux of DMS in a biologically active frontal system in the southwest Pacific Ocean. Three distinct phytoplankton blooms were studied with oceanic DMS concentrations as high as 25 nmol L<sup>−1</sup>. Measurements of DMS fluxes were made using two independent methods: the eddy covariance (EC) technique using atmospheric pressure chemical ionization–mass spectrometry (API-CIMS) and the gradient flux (GF) technique from an autonomous catamaran platform. Catamaran flux measurements are relatively unaffected by airflow distortion and are made close to the water surface, where gas gradients are largest. Flux measurements were complemented by near-surface hydrographic measurements to elucidate physical factors influencing DMS emission. Individual DMS fluxes derived by EC showed significant scatter and, at times, consistent departures from the Coupled Ocean–Atmosphere Response Experiment gas transfer algorithm (COAREG). A direct comparison between the two flux methods was carried out to separate instrumental effects from environmental effects and showed good agreement with a regression slope of 0.96 (<i>r</i><sup>2</sup> = 0.89). A period of abnormal downward atmospheric heat flux enhanced near-surface ocean stratification and reduced turbulent exchange, during which GF and EC transfer velocities showed good agreement but modelled COAREG values were significantly higher. The transfer velocity derived from near-surface ocean turbulence measurements on a spar buoy compared well with the COAREG model in general but showed less variation. This first direct comparison between EC and GF fluxes of DMS provides confidence in compilation of flux estimates from both techniques, as well as in the stable periods when the observations are not well predicted by the COAREG model.https://www.atmos-chem-phys.net/18/5861/2018/acp-18-5861-2018.pdf
collection DOAJ
language English
format Article
sources DOAJ
author M. J. Smith
C. F. Walker
T. G. Bell
T. G. Bell
M. J. Harvey
E. S. Saltzman
C. S. Law
C. S. Law
spellingShingle M. J. Smith
C. F. Walker
T. G. Bell
T. G. Bell
M. J. Harvey
E. S. Saltzman
C. S. Law
C. S. Law
Gradient flux measurements of sea–air DMS transfer during the Surface Ocean Aerosol Production (SOAP) experiment
Atmospheric Chemistry and Physics
author_facet M. J. Smith
C. F. Walker
T. G. Bell
T. G. Bell
M. J. Harvey
E. S. Saltzman
C. S. Law
C. S. Law
author_sort M. J. Smith
title Gradient flux measurements of sea–air DMS transfer during the Surface Ocean Aerosol Production (SOAP) experiment
title_short Gradient flux measurements of sea–air DMS transfer during the Surface Ocean Aerosol Production (SOAP) experiment
title_full Gradient flux measurements of sea–air DMS transfer during the Surface Ocean Aerosol Production (SOAP) experiment
title_fullStr Gradient flux measurements of sea–air DMS transfer during the Surface Ocean Aerosol Production (SOAP) experiment
title_full_unstemmed Gradient flux measurements of sea–air DMS transfer during the Surface Ocean Aerosol Production (SOAP) experiment
title_sort gradient flux measurements of sea–air dms transfer during the surface ocean aerosol production (soap) experiment
publisher Copernicus Publications
series Atmospheric Chemistry and Physics
issn 1680-7316
1680-7324
publishDate 2018-04-01
description Direct measurements of marine dimethylsulfide (DMS) fluxes are sparse, particularly in the Southern Ocean. The Surface Ocean Aerosol Production (SOAP) voyage in February–March 2012 examined the distribution and flux of DMS in a biologically active frontal system in the southwest Pacific Ocean. Three distinct phytoplankton blooms were studied with oceanic DMS concentrations as high as 25 nmol L<sup>−1</sup>. Measurements of DMS fluxes were made using two independent methods: the eddy covariance (EC) technique using atmospheric pressure chemical ionization–mass spectrometry (API-CIMS) and the gradient flux (GF) technique from an autonomous catamaran platform. Catamaran flux measurements are relatively unaffected by airflow distortion and are made close to the water surface, where gas gradients are largest. Flux measurements were complemented by near-surface hydrographic measurements to elucidate physical factors influencing DMS emission. Individual DMS fluxes derived by EC showed significant scatter and, at times, consistent departures from the Coupled Ocean–Atmosphere Response Experiment gas transfer algorithm (COAREG). A direct comparison between the two flux methods was carried out to separate instrumental effects from environmental effects and showed good agreement with a regression slope of 0.96 (<i>r</i><sup>2</sup> = 0.89). A period of abnormal downward atmospheric heat flux enhanced near-surface ocean stratification and reduced turbulent exchange, during which GF and EC transfer velocities showed good agreement but modelled COAREG values were significantly higher. The transfer velocity derived from near-surface ocean turbulence measurements on a spar buoy compared well with the COAREG model in general but showed less variation. This first direct comparison between EC and GF fluxes of DMS provides confidence in compilation of flux estimates from both techniques, as well as in the stable periods when the observations are not well predicted by the COAREG model.
url https://www.atmos-chem-phys.net/18/5861/2018/acp-18-5861-2018.pdf
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