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  • 1
    In: Biogeosciences, Copernicus GmbH, Vol. 19, No. 3 ( 2022-02-04), p. 701-714
    Abstract: Abstract. Our understanding of the biogeochemical cycling of the climate-relevant trace gas dimethyl sulfide (DMS) in the Peruvian upwelling system is still limited. Here we present oceanic and atmospheric DMS measurements which were made during two shipborne cruises in December 2012 (M91) and October 2015 (SO243) in the Peruvian upwelling region. Dimethylsulfoniopropionate (DMSP) and dimethyl sulfoxide (DMSO) were also measured during M91. DMS concentrations were 1.9 ± 0.9 and 2.5 ± 1.9 nmol L−1 in surface waters in October 2015 and December 2012, respectively. Nutrient availability appeared to be the main driver of the observed variability in the surface DMS distributions in the coastal areas. DMS, DMSP, and DMSO showed maxima in the surface layer, and no elevated concentrations associated with the oxygen minimum zone off Peru were measured. The possible role of DMS, DMSP, and DMSO as radical scavengers (stimulated by nitrogen limitation) is supported by their negative correlations with N:P (sum of nitrate and nitrite : dissolved phosphate) ratios. Large variations in atmospheric DMS mole fractions were measured during M91 (144.6 ± 95.0 ppt) and SO243 (91.4 ± 55.8 ppt); however, the atmospheric mole fractions were generally low, and the sea-to-air flux was primarily driven by seawater DMS. The Peruvian upwelling region was identified as a source of atmospheric DMS in December 2012 and October 2015. However, in comparison to the previous measurements in the adjacent regions, the Peru upwelling was a moderate source of DMS emissions at either time (M91: 5.9 ± 5.3 µmol m−2 d−1; SO243: 3.8 ± 2.7 µmol m−2 d−1).
    Type of Medium: Online Resource
    ISSN: 1726-4189
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2022
    detail.hit.zdb_id: 2158181-2
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  • 2
    In: Global Biogeochemical Cycles, American Geophysical Union (AGU), Vol. 35, No. 6 ( 2021-06)
    Abstract: Surface seawater dimethylsulfide (DMS) concentrations remain unchanged after sea ice retreat in the western Canada Basin Increased wind speed is a critical factor driving the enhancement of dimethylsulfide (DMS) flux after sea ice retreat at high latitudes in the Arctic Ocean Nutrient supply is hypothesized to significantly impact dimethylsulfide (DMS) distribution in the western Arctic Ocean
    Type of Medium: Online Resource
    ISSN: 0886-6236 , 1944-9224
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 2021
    detail.hit.zdb_id: 2021601-4
    SSG: 12
    SSG: 13
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  • 3
    Online Resource
    Online Resource
    Copernicus GmbH ; 2022
    In:  Biogeosciences Vol. 19, No. 20 ( 2022-10-28), p. 5021-5040
    In: Biogeosciences, Copernicus GmbH, Vol. 19, No. 20 ( 2022-10-28), p. 5021-5040
    Abstract: Abstract. Climate-relevant trace gas air–sea exchange exerts an important control on air quality and climate, especially in remote regions of the planet such as the Southern Ocean. It is clear that polar regions exhibit seasonal trends in productivity and biogeochemical cycling, but almost all of the measurements there are skewed to summer months. If we want to understand how the Southern Ocean affects the balance of climate through trace gas air–sea exchange, it is essential to expand our measurement database over greater temporal and spatial scales, including all seasons. Therefore, in this study, we report measured concentrations of dimethylsulfide (DMS, as well as related sulfur compounds) and isoprene in the Atlantic sector of the Southern Ocean during the winter to understand the spatial and temporal distribution in comparison to current knowledge and climatological calculations for the Southern Ocean. The observations of isoprene are the first in the winter season in the Southern Ocean. We found that the concentrations of DMS from the surface seawater and air in the investigated area were 1.03 ± 0.98 nmol−1 and 28.80 ±  12.49 pptv, respectively. The concentrations of isoprene in surface seawater were 14.46 ± 12.23 pmol−1. DMS and isoprene fluxes were 4.04 ± 4.12 µmol m−2 d−1 and 80.55 ± 78.57 nmol m−2 d−1, respectively. These results are generally lower than the values presented or calculated in currently used climatologies and models. More data are urgently needed to better interpolate climatological values and validate process-oriented models, as well as to explore how finer measurement resolution, both spatially and temporally, can influence air–sea flux calculations.
    Type of Medium: Online Resource
    ISSN: 1726-4189
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2022
    detail.hit.zdb_id: 2158181-2
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  • 4
    In: Biogeosciences, Copernicus GmbH, Vol. 15, No. 2 ( 2018-02-01), p. 649-667
    Abstract: Abstract. Parameterizations of surface ocean isoprene concentrations are numerous, despite the lack of source/sink process understanding. Here we present isoprene and related field measurements in the mixed layer from the Indian Ocean and the eastern Pacific Ocean to investigate the production and consumption rates in two contrasting regions, namely oligotrophic open ocean and the coastal upwelling region. Our data show that the ability of different phytoplankton functional types (PFTs) to produce isoprene seems to be mainly influenced by light, ocean temperature, and salinity. Our field measurements also demonstrate that nutrient availability seems to have a direct influence on the isoprene production. With the help of pigment data, we calculate in-field isoprene production rates for different PFTs under varying biogeochemical and physical conditions. Using these new calculated production rates, we demonstrate that an additional significant and variable loss, besides a known chemical loss and a loss due to air–sea gas exchange, is needed to explain the measured isoprene concentration. We hypothesize that this loss, with a lifetime for isoprene between 10 and 100 days depending on the ocean region, is potentially due to degradation or consumption by bacteria.
    Type of Medium: Online Resource
    ISSN: 1726-4189
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2018
    detail.hit.zdb_id: 2158181-2
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