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  • 1
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    Fluxes and gas transfer rates of the biogenic trace gas DMS derived from atmospheric gradients (2010)
    American Geophysical Union
    Details
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2004. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research 109 (2004): C08S10, doi:10.1029/2003JC001795.
    Description: Gas transfer rates were determined from vertical profile measurements of atmospheric dimethylsulfide (DMS) gradients over the equatorial Pacific Ocean obtained during the GasEx-2001 cruise. A quadratic relationship between gas transfer velocity and wind speed was derived from the DMS flux measurements; this relationship was in close agreement with a parameterization derived from relaxed eddy accumulation measurements of DMS over the northeastern Pacific Ocean. However, the GasEx-2001 relationship results in gas transfer rates that are a factor 2 higher than gas transfer rates calculated from a parameterization that is based on coincident eddy correlation measurements of CO2 flux. The measurement precision of both the profiling and eddy correlation techniques applied during GasEx-2001 is comparable; the two gas transfer data sets are in agreement within their uncertainty. Differences in the number of samples and the wind speed range over which CO2 and DMS fluxes were measured are likely causes for the observed discrepancy.
    Description: Funding for this work came from the Netherlands Organization for Scientific Research (NWO) and from the NOP project 951203: ‘‘Micrometeorology of air/sea fluxes of carbon dioxide. This work was supported by the Global Carbon Cycle project of the NOAA Office of Global Programs grant NA17RJ1223, National Science Foundation grant OCE-9986724, and NSF grant ATM-0120569.
    Keywords: Dimethylsulfide (DMS) ; Atmospheric gradients ; Micrometeorology ; GasEx-2001
    Repository Name: Woods Hole Open Access Server
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  • 2
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    Physical exchanges at the air–sea interface : UK–SOLAS field measurements (2010)
    American Meteorological Society
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    Publication Date: 2022-05-25
    Description: Author Posting. © American Meteorological Society, 2009. This article is posted here by permission of The UK–SOLAS projects were funded by the Natural Environment Research Council Grants NE/C001826/1 (HiWASE), NE/C001842/1 (SEASAW), NE/C001702/1 (DOGEE), and NE/E011489/1 (DMS Fluxes); and by NSF Grants ATM05-26341 (Hawaii), OCE-0623450 (Miami), and NSF-OCE 0549887/0834340/0550000 (APL-UW). for personal use, not for redistribution. The definitive version was published in Bulletin of the American Meteorological Society 90 (2009): 629-644, doi:10.1175/2008BAMS2578.1.
    Description: As part of the U.K. contribution to the international Surface Ocean–Lower Atmosphere Study, a series of three related projects—DOGEE, SEASAW, and HiWASE—undertook experimental studies of the processes controlling the physical exchange of gases and sea spray aerosol at the sea surface. The studies share a common goal: to reduce the high degree of uncertainty in current parameterization schemes. The wide variety of measurements made during the studies, which incorporated tracer and surfactant release experiments, included direct eddy correlation fluxes, detailed wave spectra, wind history, photographic retrievals of whitecap fraction, aerosol-size spectra and composition, surfactant concentration, and bubble populations in the ocean mixed layer. Measurements were made during three cruises in the northeast Atlantic on the RRS Discovery during 2006 and 2007; a fourth campaign has been making continuous measurements on the Norwegian weather ship Polarfront since September 2006. This paper provides an overview of the three projects and some of the highlights of the measurement campaigns.
    Description: As part of the U.K. contribution to the international Surface Ocean–Lower Atmosphere Study, a series of three related projects—DOGEE, SEASAW, and HiWASE—undertook experimental studies of the processes controlling the physical exchange of gases and sea spray aerosol at the sea surface. The studies share a common goal: to reduce the high degree of uncertainty in current parameterization schemes. The wide variety of measurements made during the studies, which incorporated tracer and surfactant release experiments, included direct eddy correlation fluxes, detailed wave spectra, wind history, photographic retrievals of whitecap fraction, aerosol-size spectra and composition, surfactant concentration, and bubble populations in the ocean mixed layer. Measurements were made during three cruises in the northeast Atlantic on the RRS Discovery during 2006 and 2007; a fourth campaign has been making continuous measurements on the Norwegian weather ship Polarfront since September 2006. This paper provides an overview of the three projects and some of the highlights of the measurement campaigns.
    Repository Name: Woods Hole Open Access Server
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  • 3
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    Gradients in dimethylsulfide, dimethylsulfoniopropionate, dimethylsulfoxide, and bacteria near the sea surface (2011)
    Inter-Research
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    Publication Date: 2022-05-25
    Description: Author Posting. © Inter-Research, 2005. This article is posted here by permission of Inter-Research for personal use, not for redistribution. The definitive version was published in Marine Ecology Progress Series 295 (2005): 33-42, doi:10.3354/meps295033.
    Description: Gradients of dimethylsulfide (DMS), dimethylsulfoniopropionate (DMSP), dimethylsulfoxide (DMSO), and bacterial numbers and diversity from the surface microlayer to 500 cm depth were assessed in coastal waters surrounding the Martha’s Vineyard Coastal Observatory, Massachusetts, USA. Microlayer samples were collected with a surface skimmer: a partially submerged, rotating glass cylinder (‘drum’) that allows the collection of a thin layer of water by adherence to the drum. A depletion of DMS towards the water surface (10 cm) was found at all sampling days, with largest gradients during rough sea surface conditions. The steep gradients show that gas fluxes and transfer velocities, based on the concentration disequilibrium between the water and the atmosphere, need to be based on near surface gas concentration values. Elevated DMSP, DMSO concentrations and bacterial numbers were found at the sea surface during calm conditions. Although degassing and photo-oxidation on the skimmer will bias the microlayer data, the results indicate stratification of DMSP, DMSO and bacteria during periods of smooth sea surface conditions.
    Description: We also thank the postdoctoral scholar program at the Woods Hole Oceanographic Institution, with funding provided by the J. Seward Johnson Fund.
    Keywords: Marine sulfur ; Bacteria ; Depth profiles ; Microlayer sampling ; Coastal waters ; DMS ; DMSP ; DMSO
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  • 4
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    Sea-to-air fluxes from measurements of the atmospheric gradient of dimethylsulfide and comparison with simultaneous relaxed eddy accumulation measurements (2010)
    American Geophysical Union
    Details
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2004. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research 109 (2004): C01026, doi:10.1029/2002JC001617.
    Description: We measured vertical profiles of dimethylsulfide (DMS) in the atmospheric marine boundary layer from R/P FLIP during the 2000 FAIRS cruise. Applying Monin-Obukhov similarity theory to the DMS gradients and simultaneous micrometeorological data, we calculated sea-to-air DMS fluxes for 34 profiles. From the fluxes and measured seawater DMS concentrations, we calculated the waterside gas transfer velocity, kw. Gas transfer velocities from the gradient flux approach are within the range of previous commonly used parameterizations of kw as a function of wind speed but are a factor of 2 smaller than simultaneous determinations of transfer velocity using the relaxed eddy accumulation technique. This is the first field comparison of these different techniques for measuring DMS flux from the ocean; the accuracy of the techniques and possible reasons for the discrepancy are discussed.
    Description: This work was supported in part by funds from the Woods Hole Oceanographic Institution, NSF grant ATM-0120569, ONR grant N00014-00-1-0403, and NOAA CICOR grant NA87RJ0445.
    Keywords: Air-sea exchange ; Gas transfer ; Sulfur emissions
    Repository Name: Woods Hole Open Access Server
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  • 5
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    Metabolism of dimethylsulfoniopropionate (DMSP) by juvenile Atlantic menhaden Brevoortia tyrannus (2011)
    Inter-Research
    Details
    Publication Date: 2022-05-25
    Description: Author Posting. © Inter-Research, 2006. This article is posted here by permission of Inter-Research for personal use, not for redistribution. The definitive version was published in Marine Ecology Progress Series 322 (2006): 239-248, doi:10.3354/meps322239.
    Description: Dimethylsulfoniopropionate (DMSP) synthesized by marine phytoplankton is the principal source of dimethylsulfide (DMS), an important climate-affecting gas. Prior research has demonstrated that grazing by invertebrate phytoplanktivores often affects the dynamics of DMS production from algal DMSP, but the effects of grazing by phytoplanktivorous fish have not previously been investigated. We studied the fate of algal DMSP following grazing by juvenile Atlantic menhaden Brevoortia tyrannus (13 cm fork length), which are generally viewed as the most specialized for phytoplanktivory of all postlarval fish. The menhaden were fed the dinoflagellate Prorocentrum micans, containing 1 to 2 pmol DMSP cell–1. During the first 24 h following ingestion of algal DMSP, almost none of the DMSP (ca. 1%) appeared as DMS. About 21% of ingested DMSP appeared in the water column as dissolved DMSP, peaking in concentration 9 to 11 h after feeding; in natural settings, this fraction would be poised for microbial metabolism, including potential conversion to DMS in surface waters from which outgassing to the atmosphere could occur. About 10% of ingested DMSP appeared in fecal pellets that tended to sink rapidly toward the bottom of the tanks. About 33% of ingested DMSP was deposited in the tissues of the menhaden, in particular in the red and white swimming muscles, in which we observed concentrations exceeding 0.7 µmol g–1. This final fraction could ultimately be metabolized to DMS, or it could be passed up food chains and possibly act as a taste factor in commercially important piscivores such as striped bass and bluefish. In total, our research demonstrated that at least two-thirds of the ingested DMSP ends up in tissues or feces or in solution in the ambient water in the first 24 h after feeding, and virtually none is converted to ambient DMS during that time period.
    Description: Financial support came from Michigan State University (R.W.H. sabbatical) and National Science Foundation, Division of Ocean Sciences Grant nos. OCE-9411497 and OCE-9102532.
    Keywords: Dimethylsulfide ; Dimethylsulfoniopropionate ; Menhaden ; DMS ; DMSP ; Brevoortia tyrannus ; Taste factor ; Phytoplanktivory
    Repository Name: Woods Hole Open Access Server
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  • 6
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    High concentrations and turnover rates of DMS, DMSP and DMSO in Antarctic sea ice (2012)
    American Geophysical Union
    Details
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2011. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geophysical Research Letters 38 (2011): L23609, doi:10.1029/2011GL049712.
    Description: The vast Antarctic sea-ice zone (SIZ) is a potentially significant source of the climate-active gas dimethylsulfide (DMS), yet few data are available on the concentrations and turnover rates of DMS and the related compounds dimethylsulfoniopropionate (DMSP) and dimethylsulfoxide (DMSO) in sea ice environments. Here we present new measurements characterizing the spatial variability of DMS, DMSP, and DMSO concentrations across the Antarctic SIZ, and results from tracer experiments quantifying the production rates of DMS from various sources. We observed extremely high concentrations (〉200 nM) and turnover rates (〉100 nM d−1) of DMS in sea-ice brines, indicating intense cycling of DMS/P/O. Our results demonstrate a previously unrecognized role for DMSO reduction as a major pathway of DMS production in Antarctic sea ice.
    Description: This work was supported in part by Woods Hole Oceanographic Institution’s Ocean Life Institute and by NSF grant ANT-0838872 to KRA.
    Description: 2012-06-14
    Keywords: DMS ; DMSO ; DMSP ; Sea ice
    Repository Name: Woods Hole Open Access Server
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  • 7
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    Environmental, biochemical and genetic drivers of DMSP degradation and DMS production in the Sargasso Sea (2012)
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    Publication Date: 2022-05-25
    Description: Author Posting. © The Author(s), 2011. This is the author's version of the work. It is posted here by permission of John Wiley & Sons for personal use, not for redistribution. The definitive version was published in Environmental Microbiology 14 (2012): 1210-1223, doi:10.1111/j.1462-2920.2012.02700.x.
    Description: Dimethylsulfide (DMS) is a climatically relevant trace gas produced and cycled by the surface ocean food web. Mechanisms driving intraannual variability in DMS production and dimethylsulfoniopropionate (DMSP) degradation in open-ocean, oligotrophic regions were investigated during a 10 month time-series at the Bermuda Atlantic Time-series Study site in the Sargasso Sea. Abundance and transcription of bacterial DMSP degradation genes, DMSP lyase enzyme activity, and DMS and DMSP concentrations, consumption rates, and production rates were quantified over time and depth. This interdisciplinary dataset was used to test current hypotheses of the role of light and carbon supply in regulating upper-ocean sulfur cycling. Findings supported UV-A dependent phytoplankton DMS production. Bacterial DMSP degraders may also contribute significantly to DMS production when temperatures are elevated and UV-A dose is moderate, but may favor DMSP demethylation under low UV-A doses. Three groups of bacterial DMSP degraders with distinct intraannual variability were identified and niche differentiation was indicated. The combination of genetic and biochemical data suggest a modified ‘bacterial switch’ hypothesis where the prevalence of different bacterial DMSP degradation pathways is regulated by a complex set of factors including carbon supply, temperature, and UV-A dose.
    Description: This research was funded by National Science Foundation (NSF) grants OCE- 0525928, OCE-072417, and OCE-042516. Additional funding was provided by the NSF Center for Microbial Oceanography Research and Education (CMORE), the Gordon and Betty Moore Foundation, the Scurlock Fund, the Ocean Ventures Fund, a National Defense Science and Engineering Graduate Fellowship, and an Environmental Protection Agency STAR Graduate Fellowship.
    Repository Name: Woods Hole Open Access Server
    Type: Preprint
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  • 8
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    Dimethylsulfide emissions over the multi-year ice of the western Weddell Sea (2010)
    American Geophysical Union
    Details
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2008. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geophysical Research Letters 35 (2008): L06603, doi:10.1029/2007GL031847.
    Description: This study, conducted in December 2004, is the first to present observations of DMS in a snow pack covering the multi-year sea ice of the western Weddell Sea. The snow layer is important because it is the interface through which DMS needs to be transported in order to be emitted directly from the ice to the overlying atmosphere. High concentrations of DMS, up to 6000 nmol m−3, were found during the first weeks of December but concentrations sharply decline as late spring-early summer progresses. This implies that DMS contained in sea ice is efficiently vented through the snow into the atmosphere. Indeed, field measurements by relaxed eddy accumulation indicate an average release of 11 μmol DMS m−2 d−1 from the ice and snow throughout December.
    Description: This work was financially supported by the Marie Curie Training Site Fellowship (contract HPMF-CT-2002-01865), by NERC (award NER/B/S/2003/00844) and by the U.S. National Science Foundation (OCE-0327601, and OCE-0425166).
    Keywords: Dimethylsulfide ; Multi-year ice ; Weddell Sea
    Repository Name: Woods Hole Open Access Server
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  • 9
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    Environmental turbulent mixing controls on air-water gas exchange in marine and aquatic systems (2010)
    American Geophysical Union
    Details
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2007. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geophysical Research Letters 34 (2007): L10601, doi:10.1029/2006GL028790.
    Description: Air-water gas transfer influences CO2 and other climatically important trace gas fluxes on regional and global scales, yet the magnitude of the transfer is not well known. Widely used models of gas exchange rates are based on empirical relationships linked to wind speed, even though physical processes other than wind are known to play important roles. Here the first field investigations are described supporting a new mechanistic model based on surface water turbulence that predicts gas exchange for a range of aquatic and marine processes. Findings indicate that the gas transfer rate varies linearly with the turbulent dissipation rate to the inline equation power in a range of systems with different types of forcing - in the coastal ocean, in a macro-tidal river estuary, in a large tidal freshwater river, and in a model (i.e., artificial) ocean. These results have important implications for understanding carbon cycling.
    Description: This research was performed and the manuscript prepared with support from: the National Science Foundation (OCE-03-27256, OCE-05-26677, ATM 01-20569, and DEB-05-32075), the Office of Naval Research Young Investigator Program (N00014-04-1-0621), the Hudson River Foundation (010/02A), NOAA (NA03OAR4320179), the Marie Curie Training Site Fellowship (HPMFCT- 2002-01865), the NERC (NER/B/S/2003/00844), the David and Lucille Packard Foundation, and the LDEO Climate Center.
    Keywords: Air-sea gas exchange ; Turbulent dissipation rate ; Carbon
    Repository Name: Woods Hole Open Access Server
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  • 10
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    Rain-induced turbulence and air-sea gas transfer (2010)
    American Geophysical Union
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    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2009. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research 114 (2009): C07009, doi:10.1029/2008JC005008.
    Description: Results from a rain and gas exchange experiment (Bio2 RainX III) at the Biosphere 2 Center demonstrate that turbulence controls the enhancement of the air-sea gas transfer rate (or velocity) k during rainfall, even though profiles of the turbulent dissipation rate ɛ are strongly influenced by near-surface stratification. The gas transfer rate scales with ɛ inline equation for a range of rain rates with broad drop size distributions. The hydrodynamic measurements elucidate the mechanisms responsible for the rain-enhanced k results using SF6 tracer evasion and active controlled flux technique. High-resolution k and turbulence results highlight the causal relationship between rainfall, turbulence, stratification, and air-sea gas exchange. Profiles of ɛ beneath the air-sea interface during rainfall, measured for the first time during a gas exchange experiment, yielded discrete values as high as 10−2 W kg−1. Stratification modifies and traps the turbulence near the surface, affecting the enhancement of the transfer velocity and also diminishing the vertical mixing of mass transported to the air-water interface. Although the kinetic energy flux is an integral measure of the turbulent input to the system during rain events, ɛ is the most robust response to all the modifications and transformations to the turbulent state that follows. The Craig-Banner turbulence model, modified for rain instead of breaking wave turbulence, successfully predicts the near-surface dissipation profile at the onset of the rain event before stratification plays a dominant role. This result is important for predictive modeling of k as it allows inferring the surface value of ɛ fundamental to gas transfer.
    Description: This work was funded by a generous grant from the David and Lucile Packard Foundation and the Lamont-Doherty Earth Observatory Climate Center. Additional funding was provided by the National Science Foundation (OCE-05-26677) and the Office of Naval Research Young Investigator Program (N00014-04-1-0621).
    Keywords: Turbulence ; Rain ; Gas transfer
    Repository Name: Woods Hole Open Access Server
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