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  • 2015-2019  (328)
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  • 1
    In: Frontiers in Marine Science, Lausanne : Frontiers Media, 2014, Bd. 4 (2017), Article 18, 2296-7745
    In: volume:4
    In: year:2017
    Type of Medium: Online Resource
    Pages: Diagramme, Karten
    ISSN: 2296-7745
    Language: English
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  • 2
    Publication Date: 2021-02-08
    Description: Molybdenum (Mo) concentrations and isotope compositions in sediments and shales are commonly used as proxies for anoxic and sulfidic (i.e., euxinic) conditions in the water column of paleo-marine systems. A basic assumption underlying this practice is that the proxy signal extracted from the geological record is controlled by long-term (order of decades to millennia) Mo scavenging in the euxinic water column rather than Mo deposition during brief episodes or events (order of weeks to months). To test whether this assumption is viable we studied the biogeochemical cycling of Mo and its isotopes in sediments of the intermittently euxinic Gotland Deep in the central Baltic Sea. Here, multiannual to decadal periods of euxinia are occasionally interrupted by inflow events during which well‑oxygenated water from the North Sea penetrates into the basin. During these events manganese (Mn) (oxyhydr)oxide minerals are precipitated in the water column, which are known to scavenge Mo. We present sediment and pore water Mo and Mo isotope data for sediment cores which were taken before and after a series of inflow events between 2014 and 2016. After seawater inflow, pore water Mo concentrations in anoxic surface sediments exceed the salinity-normalized concentration by more than two orders of magnitude and coincide with transient peaks of dissolved Mn. A fraction of the Mo liberated into the pore water is transported by diffusion in a downward direction and sequestered by organic matter within the sulfidic zone of the sediment. Diffusive flux calculations as well as a mass balance that is based on the sedimentary Mo isotope composition suggest that about equal proportions of the Mo accumulating in the basin are delivered by Mn (oxyhydr)oxide minerals during inflow events and Mo scavenging with hydrogen sulfide during euxinic periods. Since the anoxic surface sediment where Mo is released from Mn (oxyhydr)oxides are separated by several centimeters from the deeper sulfidic layers where Mo is removed, the solid phase record of Mo concentration and isotope composition would be misinterpreted if steady state Mo accumulation was assumed. Based on our observations in the Gotland Deep, we argue that short-term redox fluctuations need to be considered when interpreting Mo-based paleo-records.
    Type: Article , PeerReviewed
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    Format: other
    Format: other
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  • 3
    Publication Date: 2020-02-06
    Type: Article , PeerReviewed
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  • 4
    Publication Date: 2019-09-23
    Description: Oxygen minimum zones (OMZs) that impinge on continental margins favor the release of phosphorus (P) from the sediments to the water column, enhancing primary productivity and the maintenance or expansion of low-oxygen waters. A comprehensive field program in the Peruvian OMZ was undertaken to identify the sources of benthic P at six stations, including the analysis of particles from the water column, surface sediments, and pore fluids, as well as in situ benthic flux measurements. A major fraction of solid-phase P was bound as particulate inorganic P (PIP) both in the water column and in sediments. Sedimentary PIP increased with depth in the sediment at the expense of particulate organic P (POP). The ratio of particulate organic carbon (POC) to POP exceeded the Redfield ratio both in the water column (202 ± 29) and in surface sediments (303 ± 77). However, the POC to total particulate P (TPP = POP + PIP) ratio was close to Redfield in the water column (103 ± 9) and in sediment samples (102 ± 15). This suggests that the relative burial efficiencies of POC and TPP are similar under low-oxygen conditions and that the sediments underlying the anoxic waters on the Peru margin are not depleted in P compared to Redfield. Benthic fluxes of dissolved P were extremely high (up to 1.04 ± 0.31 mmol m−2 d−1), however, showing that a lack of oxygen promotes the intensified release of dissolved P from sediments, whilst preserving the POC / TPP burial ratio. Benthic dissolved P fluxes were always higher than the TPP rain rate to the seabed, which is proposed to be caused by transient P release by bacterial mats that had stored P during previous periods when bottom waters were less reducing. At one station located at the lower rim of the OMZ, dissolved P was taken up by the sediments, indicating ongoing phosphorite formation. This is further supported by decreasing porewater phosphate concentrations with sediment depth, whereas solid-phase P concentrations were comparatively high.
    Type: Article , PeerReviewed
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  • 5
    Publication Date: 2019-02-01
    Description: Large quantities of the greenhouse gas methane (CH4) are stored in the seafloor. The flux of CH4 from the sediments into the water column and finally to the atmosphere is mitigated by a series of microbial methanotrophic filter systems of unknown efficiency at highly active CH4-release sites in shallow marine settings. Here, we studied CH4-oxidation and the methanotrophic community at a high-CH4-flux site in the northern North Sea (well 22/4b), where CH4 is continuously released since a blowout in 1990. Vigorous bubble emanation from the seafloor and strongly elevated CH4 concentrations in the water column (up to 42 µM) indicated that a substantial fraction of CH4 bypassed the highly active (up to ∼2920 nmol cm−3 d−1) zone of anaerobic CH4-oxidation in sediments. In the water column, we measured rates of aerobic CH4-oxidation (up to 498 nM d−1) that were among the highest ever measured in a marine environment and, under stratified conditions, have the potential to remove a significant part of the uprising CH4 prior to evasion to the atmosphere. An unusual dominance of the water-column methanotrophs by Type II methane-oxidizing bacteria (MOB) is partially supported by recruitment of sedimentary MOB, which are entrained together with sediment particles in the CH4 bubble plume. Our study thus provides evidence that bubble emission can be an important vector for the transport of sediment-borne microbial inocula, aiding in the rapid colonization of the water column by methanotrophic communities and promoting their persistence close to highly active CH4 point sources.
    Type: Article , PeerReviewed , info:eu-repo/semantics/article
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  • 6
    Publication Date: 2019-09-23
    Description: Dissolved silicon isotope compositions have been analysed for the first time in pore waters (δ30SiPW) of three short sediment cores from the Peruvian margin upwelling region with distinctly different biogenic opal content in order to investigate silicon isotope fractionation behaviour during early diagenetic turnover of biogenic opal in marine sediments. The δ30SiPW varies between +1.1‰ and +1.9‰ with the highest values occurring in the uppermost part close to the sediment–water interface. These values are of the same order or higher than the δ30Si of the biogenic opal extracted from the same sediments (+0.3‰ to +1.2‰) and of the overlying bottom waters (+1.1‰ to +1.5‰). Together with dissolved silicic acid concentrations well below biogenic opal saturation, our collective observations are consistent with the formation of authigenic alumino-silicates from the dissolving biogenic opal. Using a numerical transport-reaction model we find that approximately 24% of the dissolving biogenic opal is re-precipitated in the sediments in the form of these authigenic phases at a relatively low precipitation rate of 56 μmol Si cm−2 yr−1. The fractionation factor between the precipitates and the pore waters is estimated at −2.0‰. Dissolved and solid cation concentrations further indicate that off Peru, where biogenic opal concentrations in the sediments are high, the availability of reactive terrigenous material is the limiting factor for the formation of authigenic alumino-silicate phases.
    Type: Article , PeerReviewed
    Format: text
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  • 7
    Publication Date: 2019-02-01
    Type: Article , PeerReviewed , info:eu-repo/semantics/article
    Format: text
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  • 8
    Publication Date: 2020-11-04
    Description: In recent decades, the central North Sea has been experiencing a general trend of decreasing dissolved oxygen (O2) levels during summer. To understand potential causes driving lower O2, we investigated a 3-day period of summertime turbulence and O2 dynamics in the thermocline and bottom boundary layer (BBL). The study focuses on coupling biogeochemical with physical transport processes to identify key drivers of the O2 and organic carbon turnover within the BBL. Combining our flux observations with an analytical process-oriented approach, we resolve drivers that ultimately contribute to determining the BBL O2 levels. We report substantial turbulent O2 fluxes from the thermocline into the otherwise isolated bottom water attributed to the presence of a baroclinic near-inertial wave. This contribution to the local bottom water O2 and carbon budgets has been largely overlooked and is shown to play a role in promoting high carbon turnover in the bottom water while simultaneously maintaining high O2 concentrations. This process may become suppressed with warming climate and stronger stratification, conditions which could promote migrating algal species that potentially shift the O2 production zone higher up within the thermocline.
    Type: Article , PeerReviewed
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  • 9
    Publication Date: 2015-11-17
    Type: Report , NonPeerReviewed
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  • 10
    Publication Date: 2019-09-23
    Description: In oxic environments, nitrogen (N) is frequently a limiting nutrient for primary production and hence a controlling element in marine ecosystems. The fixed form of N, i.e. bioavailable N for primary production, is primarily in the oxidized form of nitrate (NO3-). However, in the sub-oxic environments of oxygen minimum zones (OMZs), N-species are biochemically converted to biogenic N2 gas which is then released, or lost, to the atmosphere. N-cycling under sub-oxic conditions thus diminishes the oceanic pool of bioavailable N. It has been suggested that although OMZs constitute only about 1% of global ocean volume, they account for about 20-40% of global oceanic N loss. However, to date these estimates are subject to largely uncertainties. Here, we quantify the rate of N-cycling and the associated N-loss by evaluating all terms of a benthic-pelagic nutrient transport budget at the continental margin off Peru using observations from an extensive measurement program conducted along the continental slope and shelf region at 12°S. The data set was collected during austral summer in 2013 and consists of nutrient, microstructure and CTD/O 2 profiles as well as shipboard velocity data from two research cruises, a glider swarm experiment and current time series from a moored array. To constrain the benthic contribution to the nutrient budget, benthic nutrient fluxes were measured in benthic chambers using Biogeochemical Observatory (BIGO) landers. Detailed budget determinations were performed on the upper continental slope and shelf break as well as at the shelf. Both regions were anoxic but different with regard to nutrient distribution as well as benthic nutrient release rates. Three major conclusions can be inferred from the study: (1) Unexpectedly, the results showed that diapycnal nutrient fluxes, driven by turbulent mixing caused by the breaking of non-linear internal waves, was one to two orders of magnitude larger than advective and lateral-diffusive fluxes. (2) The relative contribution of benthic nutrient fluxes to nutrient cycling was between 30% and 50%. (3) Nitrogen conversion rates on the shelf (50m-100m water depth) were an order of magnitude larger that at the continental slope (200m-300m water depth). The strong differences in the magnitude of the nutrient cycling rates most likely originate from the presence of sulfidic bottom waters that were observed on the shelf
    Type: Conference or Workshop Item , NonPeerReviewed
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