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  • 1
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    Fluid and gas fluxes from the Logatchev hydrothermal vent area (2012)
    AGU (American Geophysical Union)
    In:  Geochemistry, Geophysics, Geosystems, 13 (7). Q07007.
    Details
    Publikationsdatum: 2018-03-01
    Beschreibung: The Logatchev hydrothermal field at 14°45′N on the MAR is characterized by gas plumes that are enriched in methane and helium compared to the oceanic background. We investigated CH4 concentration and δ13C together with δ3He in the water column of that region. These data and turbidity measurements indicate that apart from the known vent fields, another vent site exists northeast of the vent field Logatchev 1. The distribution of methane and 3He concentrations along two sections were used in combination with current measurements from lowered acoustic Doppler current profilers (LADCP) to calculate the horizontal plume fluxes of these gases. According to these examinations 0.02 μmol s−1 of 3He and 0.21 mol s−1 of methane are transported in a plume that flows into a southward direction in the central part of the valley. Based on 3He measurements of vent fluid (22 ± 6 pM), we estimate a total vent flux in this region of about 900 L s−1 and a total flux of CH4 of 3.2 mol s−1.
    Materialart: Article , PeerReviewed
    Format: text
    DOI: 10.1029/2012GC004158
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  • 2
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    Fluxes and fate of dissolved methane released at the seafloor at the landward limit of the gas hydrate stability zone offshore western Svalbard (2015)
    AGU (American Geophysical Union) | Wiley
    In:  Journal of Geophysical Research: Oceans, 120 (9). pp. 6185-6201.
    Details
    Publikationsdatum: 2017-05-02
    Beschreibung: 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.
    Materialart: Article , PeerReviewed
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    DOI: 10.1002/2015JC011084
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  • 3
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    Methane cycling in the Weddell Sea determined via stable isotope ratios and CFC-11 (2004)
    AGU (American Geophysical Union)
    In:  Global Biogeochemical Cycles, 18 (2). GB2012.
    Details
    Publikationsdatum: 2018-03-16
    Beschreibung: The physical, chemical/biological processes that control the methane dynamics in the Weddell Sea are revealed by the distributions of methane (CH4), its stable carbon isotope ratio, δ13C-CH4, and the conservative transient tracer, chlorofluorocarbon-11 (CFC-11, CCl3F). In general, a nearly linear correlation between CH4 and CFC-11 concentrations was observed. Air-sea exchange is the major source of methane to this region, and the distribution of methane is controlled mainly by mixing between surface water and methane-poor Warm Deep Water. A significant influence of methane oxidation over the predominant two end-member mixing was only found in the Weddell Sea Bottom Water (WSBW) of the deep central Weddell Basin, where the turnover time of methane appears to be about 20 years. Mixing also controls most of the δ13C-CH4 distribution, but lighter than expected carbon isotopic ratios occur in the deep WSBW of the basin. From box model simulations, it appears that this “anomaly” is due to methane oxidation with a low kinetic isotope fractionation of about 1.004. The surface waters in the Weddell Sea and the Antarctic Circumpolar Current showed a general methane undersaturation of 6 to 25% with respect to the atmospheric mixing ratio. From this undersaturation and model-derived air-sea exchange rates, we estimate a net uptake of CH4 of roughly −0.5 μmol m−2 d−1 during austral autumn.
    Materialart: Article , PeerReviewed
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    DOI: 10.1029/2003GB002151
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  • 4
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    Distribution of methane in the water column of the Baltic Sea (2010)
    AGU (American Geophysical Union)
    In:  Geophysical Research Letters, 37 (12). L12604.
    Details
    Publikationsdatum: 2018-12-20
    Beschreibung: The distribution of dissolved methane in the water column of the Baltic Sea was extensively investigated. A strong correlation between the vertical density stratification, the distribution of oxygen, hydrogen sulfide, and methane has been identified. A widespread release of methane from the seafloor is indicated by increasing methane concentrations with water depth. The deep basins in the central Baltic Sea show the strongest methane enrichments in stagnant anoxic water bodies (max. 1086 nM and 504 nM, respectively), with a pronounced decrease towards the pelagic redoxcline and slightly elevated surface water concentrations (saturation values of 206% and 120%, respectively). In general the more limnic basins in the northern part of the Baltic are characterized by lower water column methane concentrations and surface water saturation values close to the atmospheric equilibrium (between 106% and 116%). In contrast, the shallow Western Baltic Sea is characterized by high saturation values up to 746%.
    Materialart: Article , PeerReviewed
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    DOI: 10.1029/2010GL043115
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  • 5
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    Measurements of the fate of gas hydrates during transit through the ocean water column (2002)
    AGU (American Geophysical Union)
    In:  Geophysical Research Letters, 29 (22). p. 2081.
    Details
    Publikationsdatum: 2018-02-20
    Beschreibung: We report on controlled experiments to document the fate of naturally occurring methane hydrate released from the sea floor (780 m, 4.3°C) by remotely operated vehicle (ROV) disturbance. Images of buoyant sediment-coated solids rising (∼0.24 m/s) from the debris cloud, soon revealed clear crystals of methane hydrate as surficial material sloughed off. Decomposition and visible degassing began close to the predicted phase boundary, yet pieces initially of ∼0.10 m size easily survived transit to the surface ocean. Smaller pieces dissolved or dissociated before reaching the surface ocean, yet effectively transferred gas to depths where atmospheric ventilation times are short relative to methane oxidation rates.
    Materialart: Article , PeerReviewed
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    DOI: 10.1029/2002GL014727
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  • 6
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    A Surface Ocean CO2 Reference Network, SOCONET and Associated Marine Boundary Layer CO2 Measurements (2019)
    Frontiers
    In:  Frontiers in Marine Science, 6 . Art.Nr. 400.
    Details
    Publikationsdatum: 2022-01-31
    Beschreibung: The Surface Ocean CO2 NETwork (SOCONET) and atmospheric Marine Boundary Layer (MBL) CO2 measurements from ships and buoys focus on the operational aspects of measurements of CO2 in both the ocean surface and atmospheric MBLs. The goal is to provide accurate pCO2 data to within 2 micro atmosphere (μatm) for surface ocean and 0.2 parts per million (ppm) for MBL measurements following rigorous best practices, calibration and intercomparison procedures. Platforms and data will be tracked in near real-time and final quality-controlled data will be provided to the community within a year. The network, involving partners worldwide, will aid in production of important products such as maps of monthly resolved surface ocean CO2 and air-sea CO2 flux measurements. These products and other derivatives using surface ocean and MBL CO2 data, such as surface ocean pH maps and MBL CO2 maps, will be of high value for policy assessments and socio-economic decisions regarding the role of the ocean in sequestering anthropogenic CO2 and how this uptake is impacting ocean health by ocean acidification. SOCONET has an open ocean emphasis but will work with regional (coastal) networks. It will liaise with intergovernmental science organizations such as Global Atmosphere Watch (GAW), and the joint committee for and ocean and marine meteorology (JCOMM). Here we describe the details of this emerging network and its proposed operations and practices
    Materialart: Article , PeerReviewed , info:eu-repo/semantics/article
    Format: text
    Format: text
    DOI: 10.3389/fmars.2019.00400
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  • 7
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    N2O emissions from the northern Benguela upwelling system (2019)
    AGU (American Geophysical Union) | Wiley
    In:  Geophysical Research Letters, 46 (6). pp. 3317-3326.
    Details
    Publikationsdatum: 2022-01-31
    Beschreibung: 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.
    Materialart: Article , PeerReviewed , info:eu-repo/semantics/article
    Format: text
    DOI: 10.1029/2018GL081648
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  • 8
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    A Harmonized Nitrous Oxide (N2O) Ocean Observation Network for the 21st Century (2019)
    Frontiers
    In:  Frontiers in Marine Science, 6 . Art.Nr. 157.
    Details
    Publikationsdatum: 2022-01-31
    Beschreibung: Nitrous oxide (N2O) is an important atmospheric trace gas involved in tropospheric warming and stratospheric ozone depletion. Estimates of the global ocean contribution to N2O emissions average 21% (range: 10 to 53%). Ongoing environmental changes such as warming, deoxygenation and acidification are affecting oceanic N2O cycling and emissions to the atmosphere. International activities over the last decades aimed at improving estimates of global N2O emissions, including (i) the MarinE MethanE and NiTrous Oxide database (MEMENTO) for archiving of quality-controlled data, and (ii) a recent large-scale inter-laboratory comparison by Working Group 143 of the Scientific Committee on Ocean Research (SCOR). To reduce uncertainties in oceanic N2O emission estimates and to characterize the spatial and temporal variability in N2O distributions in a changing ocean, we propose the establishment of a harmonized N2O Observation Network (N2O-ON) combining discrete and continuous data from various platforms. The network will integrate observations obtained by calibrated techniques, using time series measurements at fixed stations and repeated hydrographic sections on voluntary observing ships and research vessels. In addition to exploiting existing oceanographic infrastructure, we propose the establishment of central calibration facilities in selected international laboratories to improve accuracy, and ensure standardization and comparability of N2O measurements. Final data products will include a harmonized global N2O concentration and emission fields for use in model validation and projections of future oceanic N2O emissions, to inform the global research community and policy makers.
    Materialart: Article , PeerReviewed , info:eu-repo/semantics/article
    Format: text
    DOI: 10.3389/fmars.2019.00157
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  • 9
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    Constraining the Oceanic Uptake and Fluxes of Greenhouse Gases by Building an Ocean Network of Certified Stations: The Ocean Component of the Integrated Carbon Observation System, ICOS-Oceans (2019)
    Frontiers
    In:  Frontiers in Marine Science, 6 . Art.Nr. 544.
    Details
    Publikationsdatum: 2022-01-31
    Beschreibung: The European Research Infrastructure Consortium “Integrated Carbon Observation System” (ICOS) aims at delivering high quality greenhouse gas (GHG) observations and derived data products (e.g., regional GHG-flux maps) for constraining the GHG balance on a European level, on a sustained long-term basis. The marine domain (ICOS-Oceans) currently consists of 11 Ship of Opportunity lines (SOOP – Ship of Opportunity Program) and 10 Fixed Ocean Stations (FOSs) spread across European waters, including the North Atlantic and Arctic Oceans and the Barents, North, Baltic, and Mediterranean Seas. The stations operate in a harmonized and standardized way based on community-proven protocols and methods for ocean GHG observations, improving operational conformity as well as quality control and assurance of the data. This enables the network to focus on long term research into the marine carbon cycle and the anthropogenic carbon sink, while preparing the network to include other GHG fluxes. ICOS data are processed on a near real-time basis and will be published on the ICOS Carbon Portal (CP), allowing monthly estimates of CO2 air-sea exchange to be quantified for European waters. ICOS establishes transparent operational data management routines following the FAIR (Findable, Accessible, Interoperable, and Reusable) guiding principles allowing amongst others reproducibility, interoperability, and traceability. The ICOS-Oceans network is actively integrating with the atmospheric (e.g., improved atmospheric measurements onboard SOOP lines) and ecosystem (e.g., oceanic direct gas flux measurements) domains of ICOS, and utilizes techniques developed by the ICOS Central Facilities and the CP. There is a strong interaction with the international ocean carbon cycle community to enhance interoperability and harmonize data flow. The future vision of ICOS-Oceans includes ship-based ocean survey sections to obtain a three-dimensional understanding of marine carbon cycle processes and optimize the existing network design.
    Materialart: Article , PeerReviewed , info:eu-repo/semantics/article
    Format: text
    DOI: 10.3389/fmars.2019.00544
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  • 10
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    Methane in the northern Atlantic controlled by microbial oxidation and atmospheric history (1999)
    AGU (American Geophysical Union)
    In:  Geophysical Research Letters, 26 (5). pp. 587-590.
    Details
    Publikationsdatum: 2018-02-13
    Beschreibung: 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.
    Materialart: Article , PeerReviewed
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    DOI: 10.1029/1999GL900049
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