ALBERT

Description: SO277 OMAX served two scientific projects. The objectives of the first project, SMART, were to develop multi-disciplinary methodologies to detect, quantify, and model offshore groundwater reservoirs in regions dominated by carbonate geology such as the Mediterranean Sea. To this end we acquired controlled-source electromagnetic, seismic, hydroacoustic, geochemical, seafloor imagery data off Malta. Preliminary evaluation of the geophysical data show that there are resisitivity anomalies that may represent offshore freshwater aquifers. The absence of evidence for offshore springs means that these aquifers would be confined and that it will be difficult to use them in a sustainable manner. The objective of the second project, MAPACT-ETNA, is to monitor the flank of Etna volcano on Sicily which is slowly deforming seaward. Here, we deployed six seafloor geodesy stations and six ocean bottom seismometers for long-term observation (1-3 years). In addition, we mapped the seafloor off Mt. Etna and off the island of Stromboli to constrain the geological processes that control volcanic flank stability.

Description: The AL561 cruise was conducted in the framework of the project APOC (“Anthropogenic impacts on Particulate Organic Carbon cycling in the North Sea”). This collaborative project between GEOMAR, AWI, HEREON, UHH, and BUND is to understand how particulate organic carbon (POC) cycling contributes to carbon sequestration in the North Sea and how this ecosystem service is compromised and interlinked with global change and a range of human pressures include fisheries (pelagic fisheries, bottom trawling), resource extraction (sand mining), sediment management (dredging and disposal of dredged sediments) and eutrophication. The main aim of the sampling activity during AL561 cruise was to recover undisturbed sediment from high accumulation sites in the Skagerrak/Kattegat and to subsample sediment/porewater at high resolution in order to investigate sedimentation transport processes, origin of sediment/POC and mineralization processes over the last 100- 200 years. Moreover, the actual processes of sedimentation and POC degradation in the water column and benthic layer will be addressed by sampling with CTD and Lander devices. In total 9 hydroacoustic surveys (59 profiles), 4 Gravity Corer, 7 Multicorer, 3 Lander and 4 CTD stations were successfully conducted during the AL561 cruise.

Description: Bottom trawling represents the most widespread anthropogenic physical disturbance to shelf sea sediments. While trawling-induced mortality in benthic fauna has been extensively investigated, its impacts on ecosystem functioning and carbon cycling at regional scales remain unclear. Using the North Sea as an example, we address these issues by synthesizing a high-resolution dataset of bottom trawling impact on sediments, feeding this dataset into a 3-dimensional physical–biogeochemical model to estimate trawling-induced changes in biomass, bioturbation and sedimentary organic carbon, and assessing model results with field samples. Results suggest a trawling-induced net reduction in macrobenthic biomass by 10-27%. Trawling-induced resuspension and reduction of bioturbation jointly and accumulatively reduce the regional sedimentary organic carbon sequestration capacity by 21-67%, equivalent to 0.58-1.84 Mt CO2 yr-1. Our study emphasizes the need for proper management of trawling on muddy seabeds, if the natural capacity of shelf seas for carbon sequestration should be conserved and restored.

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: Highlights • Amazon shelf sediments take up seawater potassium (K) due to reverse weathering. • Amazon shelf sediments release terrigenous phosphorus (P) during resuspension. • Updated estimates of sedimentary K uptake and P release on Amazon shelf are presented. • Sedimentary K uptake on Amazon shelf corresponds to 13% of global riverine K input. • Sedimentary P release is ~5 times higher than dissolved P discharge of Amazon River. Abstract In this study, we identify and quantify processes that lead to sedimentary potassium (K) sequestration and phosphorus (P) release on the Amazon shelf. To this end, seven short sediment cores were recovered from the Amazon shelf during R/V Meteor cruise M147. All of the sediment cores investigated in this study are characterized by elevated K to aluminum (Al) ratios compared to Amazon riverine suspended matter, which indicates that seawater K+ is incorporated into the solid phase on the entire Amazon shelf. Pore water silica (Si) profiles are characterized by irregularly increasing concentrations and plateaus, thus, deviating from the asymptotic shape that is typically found in continental margin sediments. At one site, a dissolved Si plateau coincides with a K+ minimum suggesting that these solutes are incorporated into authigenic minerals, a process referred to as reverse weathering. Previous flux estimates for elements that participate in reverse weathering on the Amazon shelf were derived from pore water diffusive fluxes, reaction rates estimated from sediment incubations and solid phase extractions. In this study, we took an alternative approach, which is based on the concentration difference between shelf sediments and river suspended particles. The resulting K flux due to reverse weathering of 1.7 ∙ 1011 mol yr−1 is in agreement with previous estimates and corresponds to 13% of the global riverine dissolved K+ input. Previous studies demonstrated that Amazon riverine particulate P is partly solubilized on the Amazon shelf. However, these results are exclusively based on sediment data close to the river mouth and no distinction between terrestrial and marine sediment components was made. Here, we quantify P release from Amazon shelf sediments by comparing terrestrial P concentrations in shelf sediments with P concentrations in river suspended particles. The resulting solubilized P flux of 2.2 ∙ 1010 mol yr−1 is about five to six times higher than previous estimates and about seven times the Amazon riverine dissolved P discharge. The magnitudes of the presented fluxes imply that the alteration of riverine shelf sediments significantly affects the mean concentrations of dissolved K+ and P in the global ocean.

Description: Seamounts are abundant features on the seafloor that serve as hotspots and barriers for the dispersal of benthic organisms. The primary focus of seamount ecology has typically been on the composition and distribution of faunal communities, with far less attention given to microbial communities. Here, we investigated the microbial communities in the water column (0-3400 m depth) and sediments (619-3883 m depth, 0-16 cm below seafloor) along the ice-covered Arctic ridge system called the Langseth Ridge. We contextualized the microbial community composition with data on the benthic trophic state (i.e., organic matter, chlorophyll- a content, and porewater geochemistry) and substrate type (i.e., sponge mats, sediments, basaltic pebbles). Our results showed slow current velocities throughout the water column, a shift in the pelagic microbial community from a dominance of Bacteroidia in the 0-10 m depth towards Proteobacteria and Nitrososphaeria below the epipelagic zone. In general, the pelagic microbial communities showed a high degree of similarity between the Langseth Ridge seamounts to a northern reference site. The only notable differences were decreases in richness between ~600 m and the bottom waters (~10 m above the seafloor) that suggest a pelagic-benthic coupling mediated by filter feeding of sponges living on the seamount summits. On the seafloor, the sponge spicule mats, and polychaete worms were the principal source of variation in sedimentary biogeochemistry and the benthic microbial community structure. The porewater signature suggested that low organic matter degradation rates are accompanied by a microbial community typical of deep-sea oligotrophic environments, such as Proteobacteria, Acidimicrobiia, Dehalococcoidia, Nitrospira, and archaeal Nitrososphaeria. The combined analysis of biogeochemical parameters and the microbial community suggests that the sponges play a significant role for pelagic-benthic coupling and acted as ecosystem engineers on the seafloor of ice-covered seamounts in the oligotrophic central Arctic Ocean.

Description: Reactive iron (Fe) oxides in marine sediments may represent a source of bioavailable Fe to the ocean via reductive dissolution and sedimentary Fe release or can promote organic carbon preservation and long-term burial. Furthermore, enrichments of reactive Fe (sum of Fe oxides, carbonates and sulfides normalized to total Fe) in ancient sediments are utilized as a paleo-proxy for anoxic conditions. Considering the general importance of reactive Fe oxides in marine biogeochemistry, it is important to quantify their terrestrial sources and fate at the land-ocean interface. We applied sequential Fe extractions to sediments from the Amazon shelf to investigate the transformation of river-derived Fe oxides during early diagenesis. We found that ∼22 % of the Amazon River-derived Fe oxides are converted to Fe-containing clay minerals in Amazon shelf sediments. The incorporation of reactive Fe into authigenic clay minerals (commonly referred to as reverse weathering) is substantiated by the relationship between Fe oxide loss and potassium (K) uptake from sedimentary pore waters, which is in agreement with the previously reported Fe/K stoichiometry of authigenic clay minerals. Mass balance calculations suggest that widely applied sequential extractions do not separate Fe-rich authigenic clay minerals from reactive Fe oxides and carbonates. We conclude that the balance between terrestrial supply of reactive Fe and reverse weathering in continental margin sediments has to be taken into account in the interpretation of sedimentary Fe speciation data. Key Points - Reactive Fe is transferred from river-derived Fe oxides into Fe-containing silicate minerals during early diagenesis - Standard sequential extraction schemes do not separate Fe oxides and carbonates from authigenic silicate minerals in Amazon shelf sediments - Terrigenous supply of reactive Fe and reverse weathering need to be considered in the interpretation of sedimentary Fe speciation