ALBERT

Description: Monthly time-series data (1998–2009) of bottom water oxygen, nitrate and nitrite concentrations from the outer shelf (150 m water depth) in the oxygen minimum zone offshore Peru were coupled to a layered biogeochemical sediment model to investigate benthic-pelagic coupling over multi-annual time scales. The model includes the mineralization of four reactive pools of particulate organic carbon (POC) with lifetimes of 0.13, 1.3, 20, and 1700 year that were constrained using empirical data. Total POC rain rates to the seafloor were derived from satellite based estimates of primary production. Solute fluxes and concentrations in sediment porewater showed highly dynamic behavior over the course of a typical year. Conversion of fixed N to N2 by denitrification varied from 1.1 mmol m−2 d−1 of N in winter to 1.8 mmol m−2 d−1 of N in summer with a long term mean N loss for the shelf of 1.5 mmol m−2 d−1 of N. Fixed N loss across the whole time-series agreed very well with a previously-published vertically-integrated sediment model for coupling the benthic and pelagic N cycle in regional and global models. Dissimilatory nitrate reduction to ammonium (DNRA) emerges as a major process in the benthic N cycle, producing on average 1.9 mmol m−2 d−1 of ammonium: more than twice the rate of ammonification of organic nitrogen. The model predicts sulfide emissions from the sediment of up to 1 mmol m−2 d−1 when POC rain rate exceeds 20 mmol m−2 d−1, in agreement with past observations of benthic sulfide fluxes and sulfide plume distributions in the water column. This study demonstrates that sediments on the Peruvian shelf are not static repositories that are independent of changes taking place in the water column. Our results strongly suggest the shelf sediments must exert an important feedback on biogeochemical processes in the overlying waters, and should be considered in regional model studies.

Description: ECO2 conducted a comprehensive offshore field programme at the Norwegian storage sites Sleipner and Snøhvit and at several natural CO2 seepage sites in order to identify potential pathways for CO2 leakage through the overburden, monitor seep sites at the seabed, track and trace the spread of CO2 in ambient bottom waters, and study the response of benthic biota to CO2. Based on its extensive field programme ECO2 developed guidelines for the monitoring of sub-seabed storage sites. ECO2 recommends that overburden, seabed, and water column should be surveyed applying the following techniques: i) 3-D seismic imaging of seals and overburden, ii) high-resolution bathymetry/backscatter mapping of the seabed, iii) hydro-acoustic imaging of shallow gas accumulations in the seabed and gas bubbles ascending into the water column, iv) video/photo imaging of biota at the seabed, v) chemical detection of dissolved CO2 and related parameters in ambient bottom waters. Additional targeted studies have to be conducted if active formation water seeps, gas seeps, and pockmarks with deep roots reaching into the storage formation occur at the seabed. These sites have to be revisited on a regular basis to determine emission rates of gases and fluids and exclude that seepage is invigorated and pockmarks are re-activated by the storage operation. Baseline studies serve to determine the natural variability against which the response of the storage complex to the storage operation has to be evaluated. All measurements being part of the monitoring program, thus, need to be performed during the baseline study prior to the onset of the storage operation to assess the spatial and temporal variability of leakage-related structures, parameters, and processes.

Description: Weathering of silicate minerals is the major sink for atmospheric CO2 on geological time scales. It has commonly been assumed that this process is only occurring on land. New results, however, show that silicate minerals are also reactive within marine sediments. Most of the metabolic CO2 being produced in marine sediments enriched in organic matter is consumed by this reaction with major implications for the geological carbon cycle.

Description: In order to proceed with speculative modelling of the impacts of potential leakage of geologically stored carbon, it is necessary to develop plausible scenarios. Here a range of such scenarios are developed based on a consensus of the possible geological mechanisms of leakage, namely abandoned wells, geological faults and operational blowouts. Whilst the resulting scenarios remain highly speculative, they do enable short term progress in modelling and provide a basis for further debate and refinement.

Description: Dissolved silicate (H4SiO4) is essential for the formation of the opaline skeletal structures of diatoms and other siliceous plankton. A fraction of particulate biogenic silica (bSi) formed in surface waters sinks to the seabed, where it either dissolves and returns to the water column or is permanently buried. Global silica budgets are still poorly constrained since data on benthic bSi cycling are lacking, especially on continental margins. This study describes benthic bSi cycling in the Skagerrak, a sedimentary depocenter for particles from the North Sea. Biogenic silica burial fluxes, benthic H4SiO4 fluxes to the water column and bSi burial efficiencies are reported for nine stations by evaluating data from in-situ benthic landers and sediment cores with a diagenetic reaction-transport model. The model simulates bSi contents and H4SiO4 concentrations at all sites using a novel power law to describe bSi dissolution kinetics with a small number of adjustable parameters. Our results show that, on average, 1100 mmol m-2 yr-1 of bSi rains down to the Skagerrak basin seafloor, of which 50% is released back to overlying waters, with the remainder being buried. Biogenic silica cycling in the Skagerrak is generally consistent with previously reported global trends, showing higher Si fluxes and burial efficiencies than deep-sea sites and similar values compared to other continental margins. A significant finding of this work is a molar bSi-to-organic carbon burial ratio of 0.22 in Skagerrak sediments, which is distinctively lower compared to other continental margins. We suggest that the continuous dissolution of bSi in suspended sediments transported over long distances from the North Sea leads to the apparent decoupling between bSi and organic carbon in Skagerrak sediments.

Description: Enhanced weathering of mafic and ultra-mafic minerals has been suggested as a strategy for carbon dioxide removal (CDR) and a contribution to achieve a balance between global CO2 sources and sinks (net zero emission). This study was designed to assess CDR by dissolution of ultramafic sand (UMS) in artificial seawater (ASW). Fine grained UMS with an olivine content of ~75% was reacted in ASW for up to 134 days at 1 bar and 21.5–23.9°C. A decline in total alkalinity (TA) was observed over the course of the experiments. This unexpected result indicates that TA removal via precipitation of cation-rich authigenic phases exceeded the production of TA induced by olivine dissolution. The TA decline was accompanied by a decrease in dissolved inorganic carbon and Ca concentrations presumably induced by CaCO3 precipitation. Temporal changes in dissolved Si, Ca, Mg, and TA concentrations observed during the experiments were evaluated by a numerical model to identify secondary mineral phases and quantify rates of authigenic phase formation. The modeling indicates that CaCO3, FeOOH and a range of Mg-Si-phases were precipitated during the experiments. Chemical analysis of precipitates and reacted UMS surfaces confirmed that these authigenic phases accumulated in the batch reactors. Nickel released during olivine dissolution, a potential toxic element for certain organisms, was incorporated in the secondary phases and is thus not a suitable proxy for dissolution rates as proposed by earlier studies. The overall reaction stoichiometry derived from lab experiments was applied in a box model simulating atmospheric CO2 uptake in a continental shelf setting induced by olivine addition. The model results indicate that CO2 uptake is reduced by a factor of 5 due to secondary mineral formation and the buffering capacity of seawater. In comparable natural settings, olivine addition may thus be a less efficient CDR method than previously believed.