ALBERT

Description: This dataset contains abiotic and biotic data from sediment samples from nine sites in the Weddell Sea (mostly South-Eastern). Data are provided for sediment pigments (chlorophyll a and phaeopigment content through fluorometry), total organic carbon (TOC), total nitrogen (TN), stable isotope values of carbon and nitrogen (δ13C, δ15N) and grain size (silt&clay 〈 32 µm, very fine sand 63–125 µm sand, fine sand 125–250 µm, medium sand 250–500 µm, coarse sand 500–1000 µm, larger coarse sand 〉 1000 µm). Before the TOC and carbon isotope analysis the sediment samples were acidified to eliminate inorganic carbon. A minimum of three replicate samples (cores) were collected using a MUC10 multicorer or giant box corer. Sediment cores were subsampled with a 60-ml syringe (inner diameter 2.7 cm) for stations 017, 026, 061, 072, and with a 10-ml syringe (inner diameter 1 cm) for stations 001, 037, 048, 104, 115. Subsamples were sliced in 1-cm steps down to 5 cm depth. Detailed methods are described in Säring et al. (submitted) except for stable isotopes: Flash combustion in a Flash 2000 (Thermo) elemental analyser to a Delta V advantage (Thermo) isotope ratio masspectrometer. δ values are reported relative to atmospheric N2 (δ15N) and Vienna PeeDee Belemnite (δ13C). Reference materials for stable isotope analysis: IAEA-N1, IAEA-N2, IAEA-N3, NBS 22, IAEA-CH-3 and IAEA-CH-6; calibration material: Acetanilide (Merck). The analytical precision for both stable isotope ratios was 〈±0.2‰. Cores with the label -e (Environment) were only used to collect the above data. Environmental and fauna data were collected from cores with the label -i (Incubation). This data table is part of a larger study analysing the role of environmental parameters for meio- and macrofaunal community composition (see Related to below).

Description: Swath sonar bathymetry data used for that dataset was recorded during RV SONNE during cruise SO276 using Kongsberg EM 122 multibeam echosounder. The cruise took place between 22.06.2020 - 26.07.2020 in the Atlanic Ocean. Data were recorded throughout the whole time spend outside EEZs. The approximate average depth of the entire dataset is around 4000m. To enhance MBES data accuracy, sound velocity profile casts were conducted in the vicinity of the working area prior to the survey using CTD rosette. During transits, sound velocity profile from the WOA13 were aplied via Sound Speed Manager Software. After processing, these data were directly imported into the MBES Acquisition software Kongsberg SIS Seafloor Information System. Data were manually edited for false measurements using Qimera. Raster were calculated and stored in GeoTIFF format with a 100m resolution (negative values), WGS85 as vertical datum and UTM as a projection, both for EM122 & EM710. Data products include ungridded soundings and bathymetric grids (100 m resolution) of the entire cruise for each EM122 & EM710. The data processing and provision was accomplished within work package 2 of the EU Horizon 2020 project iAtlantic- Integrated Assessment of Atlantic Marine Ecosystem in Space and Time and the IceAge project.

Description: Raw multibeam bathymetry data were recorded on RV SONNE during SO276 using Kongsberg EM710 multibeam echosounder. The cruise took place between 22.06.2020 - 26.07.2020 in the Atlantic Ocean. Data were recorded throughout the whole time spend outside EEZs in areas shallower than 1500m with an approximate average depth of around 400m. To enhance MBES data accuracy, CTD casts were made in the working area prior to each MBES survey using CTD rosette to raytrace beams with the obtained sound velocity profiles (SVP). During transits, SVPs from the WOA13 were applied via Sound Speed Manager Software to the data directly during acquisition with SIS Seafloor Information System. Data are unprocessed and can therefore contain incorrect depth measurements (artifacts) without further processing. The data are archived at the Federal Maritime and Hydrographic Agency of Germany (Bundesamt für Seeschifffahrt und Hydrographie, BSH) and provided to PANGAEA database for data curation and publication. Ancillary sound velocity profiles (SVP) files from the cruise are archived at the BSH, thus SVP files are added to this dataset. Data acquisition and provision were accomplished within work package 2 of the EU Horizon 2020 project iAtlantic- Integrated Assessment of Atlantic Marine Ecosystem in Space and Time (https://www.iatlantic.eu/) IceAge project.

Description: The dataset is about temporal variability of dissolved methane along the freshwater-sea continuum in northern Germany. Sensors were installed at fixed stations at in total three sites at different water depths. This dataset is from the station in Cuxhaven (53.8771 N, 8.7048 E) taken at about 2-7m depth (depending on the tide). The data was obtained between 11 April and 28 August 2021 in high frequency measurements (1 min) with a methane sensor from Kongsberg (4H Jena model CONTROS HydroC CH4). Methane concentrations were calculated according to manufacturer's instructions, based on temperature and salinity values from COSYNA Container Cuxhaven. For the quality control of the data a local range of 0.1 – 1000 nmol/L was set, a technical range for the pump power 2 – 8 Watt, a spike and gradient value of 1. Due to heavy biofouling the external pump of the sensor failed, resulting in data gaps. For a more detailed description see the article cited in References.

Description: To determine the effect of the rate of temperature increase (acute vs. gradual) and magnitude as well as the timing of nutrient addition on a natural marine phytoplankton community, a bottle incubation experiment has been conducted at the Institute for Chemistry and Biology of the Marine Environment (ICBM) in Wilhelmshaven, Germany. The community was collected at the Helgoland Roads long-term time series site in the German part of the North Sea (https://deims.org/1e96ef9b-0915-4661-849f-b3a72f5aa9b1) on the 6ᵗʰ of March 2022. The surface water containing the phytoplankton community was collected from the RV HEINCKE with a pipe covered with a 200 µm net attached to a diaphragm pump. In the first experimental run, the community was exposed to either gradual or acute temperature increase (from 6 to either 12 or 18°C) with 25 different N:P supply ratios added as a batch at the beginning of the bottle incubation. Simultaneously, the same community was gradually acclimated to their experimental temperatures under ambient nutrients and was used in a second experimental run in which it received the same 25 different N:P supply ratios after temperature acclimation. The light conditions were set to 175 µmol s-1 m-2 and a day-night cycle of 12h:12h which corresponds to the natural conditions at that time of the year. With this, it was possible to test the effect of a gradual vs. acute temperature increase and the timing of nutrient addition i.e., before or after the temperature change. This experimental set-up summed up to 400 units (8 temperature treatments x 5 nitrogen levels x 5 phosphorus levels x 2 replicates). Each experimental run was ended after 12 days. Fluorescence (395/680 Exc./Em.) was measured every second day using a SYNERGY H1 microplate reader (BioTek®) to determine phototrophic growth over time. At the end of each experiment, one replicate was filtered onto pre-combusted acid-washed glass microfiber filters (WHATMAN® GF/C) for intracellular carbon (POC), nitrogen (PON), and phosphorus (POP) content. The POP filters were pre-combusted and then analysed by molybdate reaction after digestion with a potassium peroxydisulfate solution (Wetzel and Likens 2003). The POC and PON filters were dried at 60°C before they were measured in an elemental analyser (Flash EA 1112, Thermo Scientific, Walthman, MA, USA).

Description: Production pathways of the prominent volatile organic halogen compound methyl iodide (CH3I) are not fully understood. Based on observations, production of CH3I via photochemical degradation of organic material or via phytoplankton production has been proposed. Additional insights could not be gained from correlations between observed biological and environmental variables or from biogeochemical modeling to identify unambiguously the source of methyl iodide. In this study, we aim to address this question of source mechanisms with a three-dimensional global ocean general circulation model including biogeochemistry (MPIOM-HAMOCC (MPIOM - Max Planck Institute Ocean Model HAMOCC - HAMburg Ocean Carbon Cycle model)) by carrying out a series of sensitivity experiments. The simulated fields are compared with a newly available global data set. Simulated distribution patterns and emissions of CH3I differ largely for the two different production pathways. The evaluation of our model results with observations shows that, on the global scale, observed surface concentrations of CH3I can be best explained by the photochemical production pathway. Our results further emphasize that correlations between CH3I and abiotic or biotic factors do not necessarily provide meaningful insights concerning the source of origin. Overall, we find a net global annual CH3I air-sea flux that ranges between 70 and 260 Gg/yr. On the global scale, the ocean acts as a net source of methyl iodide for the atmosphere, though in some regions in boreal winter, fluxes are of the opposite direction (from the atmosphere to the ocean).

Description: Bromoform (CHBr3) is one important precursor of atmospheric reactive bromine species that are involved in ozone depletion in the troposphere and stratosphere. In the open ocean bromoform production is linked to phytoplankton that contains the enzyme bromoperoxidase. Coastal sources of bromoform are higher than open ocean sources. However, open ocean emissions are important because the transfer of tracers into higher altitude in the air, i.e. into the ozone layer, strongly depends on the location of emissions. For example, emissions in the tropics are more rapidly transported into the upper atmosphere than emissions from higher latitudes. Global spatio-temporal features of bromoform emissions are poorly constrained. Here, a global three-dimensional ocean biogeochemistry model (MPIOM-HAMOCC) is used to simulate bromoform cycling in the ocean and emissions into the atmosphere using recently published data of global atmospheric concentrations (Ziska et al., 2013) as upper boundary conditions. Our simulated surface concentrations of CHBr3 match the observations well. Simulated global annual emissions based on monthly mean model output are lower than previous estimates, including the estimate by Ziska et al. (2013), because the gas exchange reverses when less bromoform is produced in non-blooming seasons. This is the case for higher latitudes, i.e. the polar regions and northern North Atlantic. Further model experiments show that future model studies may need to distinguish different bromoform-producing phytoplankton species and reveal that the transport of CHBr3 from the coast considerably alters open ocean bromoform concentrations, in particular in the northern sub-polar and polar regions.

Description: The first long-term aerosol sampling and chemical characterization results from measurements at the Cape Verde Atmospheric Observatory (CVAO) on the island of São Vicente are presented and are discussed with respect to air mass origin and seasonal trends. In total 671 samples were collected using a high-volume PM10 sampler on quartz fiber filters from January 2007 to December 2011. The samples were analyzed for their aerosol chemical composition, including their ionic and organic constituents. Back trajectory analyses showed that the aerosol at CVAO was strongly influenced by emissions from Europe and Africa, with the latter often responsible for high mineral dust loading. Sea salt and mineral dust dominated the aerosol mass and made up in total about 80% of the aerosol mass. The 5-year PM10 mean was 47.1 ± 55.5 µg/m**2, while the mineral dust and sea salt means were 27.9 ± 48.7 and 11.1 ± 5.5 µg/m**2, respectively. Non-sea-salt (nss) sulfate made up 62% of the total sulfate and originated from both long-range transport from Africa or Europe and marine sources. Strong seasonal variation was observed for the aerosol components. While nitrate showed no clear seasonal variation with an annual mean of 1.1 ± 0.6 µg/m**3, the aerosol mass, OC (organic carbon) and EC (elemental carbon), showed strong winter maxima due to strong influence of African air mass inflow. Additionally during summer, elevated concentrations of OM were observed originating from marine emissions. A summer maximum was observed for non-sea-salt sulfate and was connected to periods when air mass inflow was predominantly of marine origin, indicating that marine biogenic emissions were a significant source. Ammonium showed a distinct maximum in spring and coincided with ocean surface water chlorophyll a concentrations. Good correlations were also observed between nss-sulfate and oxalate during the summer and winter seasons, indicating a likely photochemical in-cloud processing of the marine and anthropogenic precursors of these species. High temporal variability was observed in both chloride and bromide depletion, differing significantly within the seasons, air mass history and Saharan dust concentration. Chloride (bromide) depletion varied from 8.8 ± 8.5% (62 ± 42%) in Saharan-dust-dominated air mass to 30 ± 12% (87 ± 11%) in polluted Europe air masses. During summer, bromide depletion often reached 100% in marine as well as in polluted continental samples. In addition to the influence of the aerosol acidic components, photochemistry was one of the main drivers of halogenide depletion during the summer; while during dust events, displacement reaction with nitric acid was found to be the dominant mechanism. Positive matrix factorization (PMF) analysis identified three major aerosol sources: sea salt, aged sea salt and long-range transport. The ionic budget was dominated by the first two of these factors, while the long-range transport factor could only account for about 14% of the total observed ionic mass.

Description: The chemical characterization of filter high volume (HV) and Berner impactor (BI) samples PM during RHaMBLe (Reactive Halogens in the Marine Boundary Layer) 2007 shows that the Cape Verde aerosol particles are mainly composed of sea salt, mineral dust and associated water. Minor components are nss-salts, OC and EC. The influence from the African continent on the aerosol constitution was generally small but air masses which came from south-western Europe crossing the Canary Islands transported dust to the sampling site together with other loadings. The mean mass concentration was determined for PM10 to 17 µg/m**3 from impactor samples and to 24.2 µg/m**3 from HV filter samples. Non sea salt (nss) components of PM were found in the submicron fractions and nitrate in the coarse mode fraction. Bromide was found in all samples with much depleted concentrations in the range 1-8 ng/m**3 compared to fresh sea salt aerosol indicating intense atmospheric halogen chemistry. Loss of bromide by ozone reaction during long sampling time is supposed and resulted totally in 82±12% in coarse mode impactor samples and in filter samples in 88±6% bromide deficits. A chloride deficit was determined to 8% and 1% for the coarse mode particles (3.5-10 µm; 1.2-3.5 µm) and to 21% for filter samples. During 14 May with high mineral dust loads also the maximum of OC (1.71 µg/m**3) and EC (1.25 µg/m**3) was measured. The minimum of TC (0.25 µg/m**3) was detected during the period 25 to 27 May when pure marine air masses arrived. The concentrations of carbonaceous material decrease with increasing particle size from 60% for the ultra fine particles to 2.5% in coarse mode PM. Total iron (dust vs. non-dust: 0.53 vs. 0.06 µg/m**3), calcium (0.22 vs. 0.03 µg/m**3) and potassium (0.33 vs. 0.02 µg/m**3) were found as good indicators for dust periods because of their heavily increased concentration in the 1.2 to 3.5 µm fraction as compared to their concentration during the non-dust periods. For the organic constituents, oxalate (78-151 ng/m**3) and methanesulfonic acid (MSA, 25-100 ng/m**3) are the major compounds identified. A good correlation between nss-sulphate and MSA was found for the majority of days indicating active DMS chemistry and low anthropogenic influences.