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  • OceanRep  (4)
  • AGU (American Geophysical Union)  (4)
  • 2015-2019  (2)
  • 1995-1999  (2)
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  • OceanRep  (4)
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  • 1
    Publication Date: 2017-05-02
    Description: Widespread seepage of methane from seafloor sediments offshore Svalbard close to the landward limit of the gas hydrate stability zone (GHSZ) may, in part, be driven by hydrate destabilization due to bottom water warming. To assess whether this methane reaches the atmosphere where it may contribute to further warming, we have undertaken comprehensive surveys of methane in seawater and air on the upper slope and shelf region. Near the GHSZ limit at ∼400 m water depth, methane concentrations are highest close to the seabed, reaching 825 nM. A simple box model of dissolved methane removal from bottom waters by horizontal and vertical mixing and microbially mediated oxidation indicates that ∼60% of methane released at the seafloor is oxidized at depth before it mixes with overlying surface waters. Deep waters are therefore not a significant source of methane to intermediate and surface waters; rather, relatively high methane concentrations in these waters (up to 50 nM) are attributed to isopycnal turbulent mixing with shelf waters. On the shelf, extensive seafloor seepage at 〈100 m water depth produces methane concentrations of up to 615 nM. The diffusive flux of methane from sea to air in the vicinity of the landward limit of the GHSZ is ∼4-20 μmol m-2 d-1, which is small relative to other Arctic sources. In support of this, analyses of mole fractions and the carbon isotope signature of atmospheric methane above the seeps do not indicate a significant local contribution from the seafloor source.
    Type: Article , PeerReviewed
    Format: text
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  • 2
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    AGU (American Geophysical Union) | Wiley
    In:  Geophysical Research Letters, 46 (6). pp. 3317-3326.
    Publication Date: 2022-01-31
    Description: The Benguela Upwelling system (BUS) is the most productive of all eastern boundary upwelling ecosystems and it hosts a well‐developed oxygen minimum zone. As such, the BUS is a potential hotspot for production of N2O, a potent greenhouse gas derived from microbially‐driven decay of sinking organic matter. Yet, the extent at which near‐surface waters emit N2O to the atmosphere in the BUS is highly uncertain. Here we present the first high‐resolution surface measurements of N2O across the northern part of the BUS (nBUS). We found strong gradients with a three‐fold increase in N2O concentrations near the coast as compared with open ocean waters. Our observations show enhanced sea‐to‐air fluxes of N2O (up to 1.67 nmol m−2 s−1) in association with local upwelling cells. Based on our data we suggest that the nBUS can account for 13% of the total coastal upwelling source of N2O to the atmosphere.
    Type: Article , PeerReviewed , info:eu-repo/semantics/article
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  • 3
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    AGU (American Geophysical Union)
    In:  Geophysical Research Letters, 26 (5). pp. 587-590.
    Publication Date: 2018-02-13
    Description: During May - August, 1997, the distributions of dissolved methane and CCl3F (CFC11) were measured in the Atlantic between 50° and 60°N. In surface waters throughout the region, methane was observed to be close to equilibrium with the atmospheric mixing ratio, implying that surface ocean methane is tracking its atmospheric history in regions of North Atlantic Deep Water formation. Despite the different atmospheric history and ocean chemistry of CH4 and CFC11, their spatial distribution patterns in the water column are remarkably similar. One-dimensional distributions have been simulated with an advection-diffusion model forced by the atmospheric histories. The results suggest that the similar patterns result from the increasing input of CH4 and CFC11 to newly formed deep waters over time, combined with the effect of horizontal mixing and the oxidation of methane on a 50 year time scale.
    Type: Article , PeerReviewed
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  • 4
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    AGU (American Geophysical Union)
    In:  Global Biogeochemical Cycles, 12 (3). pp. 467-477.
    Publication Date: 2018-03-14
    Description: The δ13C of dissolved inorganic carbon was measured on samples collected at 49°N in the northeast Atlantic in January 1994. Deeper than 2000 m, δ13C exhibits the same negative correlation versus dissolved phosphate that is observed elsewhere in the deep Atlantic. Upward from 2000 m to about 600 m, δ13C shifts to values more negative than expected from the correlation with nutrients at depth, which is likely due to penetration of anthropogenic CO2. From these data, the profile of the anthropogenic δ13C decrease is calculated by using either dissolved phosphate or apparent oxygen utilization as a proxy for the preanthropogenic δ13C distribution. The shape of the anthropogenic anomaly profile derived from phosphate is similar to that of the increase in dissolved inorganic carbon derived by others in the same area. The reconstruction from oxygen utilization results in a lower estimate of the anthropogenic δ13C decrease in the upper water column, and the vertical anomaly profile is less similar to that of the dissolved inorganic carbon increase. A 13C budget for the atmosphere, ocean, and terrestrial biosphere indicates that within the range of probable ocean CO2 uptake the ratio of δ13C to inorganic carbon change should be mostly influenced by the 13C inventory change of the biosphere. However, the uncertainty in the ratio we derive prevents a strong contraint on the size of the exchangeable biosphere.
    Type: Article , PeerReviewed
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