Oceanic emissions of sulfur: Application of new techniques
Dissertation (Ph.D.) University of Alaska Fairbanks, 1998 Sulfur gases and aerosols are important in the atmosphere because they play major roles in acid rain, arctic haze, air pollution, and climate. Globally, man-made and natural sulfur emissions are comparable in magnitude. The major natural sour...
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ftunivalaska:oai:scholarworks.alaska.edu:11122/9483 2023-05-15T15:16:37+02:00 Oceanic emissions of sulfur: Application of new techniques Jodwalis, Clara Mary Benner, Richard L. 1998 http://hdl.handle.net/11122/9483 unknown http://hdl.handle.net/11122/9483 Department of Chemistry and Biochemistry Analytical chemistry Remote sensing Physical oceanography Dissertation phd 1998 ftunivalaska 2023-02-23T21:37:17Z Dissertation (Ph.D.) University of Alaska Fairbanks, 1998 Sulfur gases and aerosols are important in the atmosphere because they play major roles in acid rain, arctic haze, air pollution, and climate. Globally, man-made and natural sulfur emissions are comparable in magnitude. The major natural source is dimethyl sulfide (DMS) from the oceans, where it originates from the degradation of dimethysulfonioproprionate (DMSP), a compound produced by marine phytoplankton. Global budgets of natural sulfur emissions are uncertain because of (1) the uncertainty in the traditional method used to estimate DMS sea-to-air flux, and (2) the spatial and temporal variability of DMS sea-to-air flux. We have worked to lessen the uncertainty on both fronts. The commonly used method for estimating DMS sea-to-air flux is certain to a factor of two, at best. We used a novel instrumental technique to measure, for the first time, sulfur gas concentration fluctuations in the marine boundary layer. The measured concentration fluctuations were then used with two established micrometeorological techniques to estimate sea-to-air flux of sulfur. Both methods appear to be more accurate than the commonly used one. The analytical instrument we used in our studies shows potential as a direct flux measurement device. High primary productivity in high-latitude oceans suggests a potentially large DMS source from northern oceans. To begin to investigate this hypothesis, we have measured DMS in the air over northern oceans around Alaska. For integrating and extrapolating field measurements over larger areas and longer time periods, we have developed a model of DMS ocean mixing, biological production, and sea-to-air flux of DMS. The model's main utility is in gaining intuition on which parameters are most important to DMS sea-to-air flux. This information, along with a direct flux measurement capability, are crucial steps toward the long-term goal of remotely sensing DMS flux. A remote sensing approach will mitigate the problems of spatial and ... Doctoral or Postdoctoral Thesis Arctic Phytoplankton Alaska University of Alaska: ScholarWorks@UA Arctic Fairbanks |
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University of Alaska: ScholarWorks@UA |
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topic |
Analytical chemistry Remote sensing Physical oceanography |
spellingShingle |
Analytical chemistry Remote sensing Physical oceanography Jodwalis, Clara Mary Oceanic emissions of sulfur: Application of new techniques |
topic_facet |
Analytical chemistry Remote sensing Physical oceanography |
description |
Dissertation (Ph.D.) University of Alaska Fairbanks, 1998 Sulfur gases and aerosols are important in the atmosphere because they play major roles in acid rain, arctic haze, air pollution, and climate. Globally, man-made and natural sulfur emissions are comparable in magnitude. The major natural source is dimethyl sulfide (DMS) from the oceans, where it originates from the degradation of dimethysulfonioproprionate (DMSP), a compound produced by marine phytoplankton. Global budgets of natural sulfur emissions are uncertain because of (1) the uncertainty in the traditional method used to estimate DMS sea-to-air flux, and (2) the spatial and temporal variability of DMS sea-to-air flux. We have worked to lessen the uncertainty on both fronts. The commonly used method for estimating DMS sea-to-air flux is certain to a factor of two, at best. We used a novel instrumental technique to measure, for the first time, sulfur gas concentration fluctuations in the marine boundary layer. The measured concentration fluctuations were then used with two established micrometeorological techniques to estimate sea-to-air flux of sulfur. Both methods appear to be more accurate than the commonly used one. The analytical instrument we used in our studies shows potential as a direct flux measurement device. High primary productivity in high-latitude oceans suggests a potentially large DMS source from northern oceans. To begin to investigate this hypothesis, we have measured DMS in the air over northern oceans around Alaska. For integrating and extrapolating field measurements over larger areas and longer time periods, we have developed a model of DMS ocean mixing, biological production, and sea-to-air flux of DMS. The model's main utility is in gaining intuition on which parameters are most important to DMS sea-to-air flux. This information, along with a direct flux measurement capability, are crucial steps toward the long-term goal of remotely sensing DMS flux. A remote sensing approach will mitigate the problems of spatial and ... |
author2 |
Benner, Richard L. |
format |
Doctoral or Postdoctoral Thesis |
author |
Jodwalis, Clara Mary |
author_facet |
Jodwalis, Clara Mary |
author_sort |
Jodwalis, Clara Mary |
title |
Oceanic emissions of sulfur: Application of new techniques |
title_short |
Oceanic emissions of sulfur: Application of new techniques |
title_full |
Oceanic emissions of sulfur: Application of new techniques |
title_fullStr |
Oceanic emissions of sulfur: Application of new techniques |
title_full_unstemmed |
Oceanic emissions of sulfur: Application of new techniques |
title_sort |
oceanic emissions of sulfur: application of new techniques |
publishDate |
1998 |
url |
http://hdl.handle.net/11122/9483 |
geographic |
Arctic Fairbanks |
geographic_facet |
Arctic Fairbanks |
genre |
Arctic Phytoplankton Alaska |
genre_facet |
Arctic Phytoplankton Alaska |
op_relation |
http://hdl.handle.net/11122/9483 Department of Chemistry and Biochemistry |
_version_ |
1766346922377871360 |