ALBERT

Description: The distribution of dissolved aluminium in the West Atlantic Ocean shows a mirror image with that of dissolved silicic acid, hinting at intricate interactions between the ocean cycling of Al and Si. The marine biogeochemistry of Al is of interest because of its potential impact on diatom opal remineralisation, hence Si availability. Furthermore, the dissolved Al concentration at the surface ocean has been used as a tracer for dust input, dust being the most important source of the bio-essential trace element iron to the ocean. Previously, the dissolved concentration of Al was simulated reasonably well with only a dust source, and scavenging by adsorption on settling biogenic debris as the only removal process. Here we explore the impacts of (i) a sediment source of Al in the Northern Hemisphere (especially north of ~ 40° N), (ii) the imposed velocity field, and (iii) biological incorporation of Al on the modelled Al distribution in the ocean. The sediment source clearly improves the model results, and using a different velocity field shows the importance of advection on the simulated Al distribution. Biological incorporation appears to be a potentially important removal process. However, conclusive independent data to constrain the Al / Si incorporation ratio by growing diatoms are missing. Therefore, this study does not provide a definitive answer to the question of the relative importance of Al removal by incorporation compared to removal by adsorptive scavenging.

Description: Concentrations of dissolved (〈0.2 µm) Fe (DFe) in the Arctic shelf seas and in the surface waters of the central Arctic Ocean are presented. In the Barents and Kara seas, near-surface DFe minima indicate depletion of DFe by phytoplankton growth. Below the surface, lower DFe concentrations in the Kara Sea (~0.4-0.6 nM) than in the Barents Sea (~0.6-0.8 nM) likely reflect scavenging removal or biological depletion of DFe. Very high DFe concentrations (〉10 nM) in the bottom waters of the Laptev Sea shelf may be attributed to either sediment resuspension, sinking of brine or regeneration of DFe in the lower layers. A significant correlation (R2 = 0.60) between salinity and DFe is observed. Using d18O, salinity, nutrients and total alkalinity data, the main source for the high (〉2 nM) DFe concentrations in the Amundsen and Makarov Basins is identified as (Eurasian) river water, transported with the Transpolar Drift (TPD). On the North American side of the TPD, the DFe concentrations are low (〈0.8 nM) and variations are determined by the effects of sea-ice meltwater, biological depletion and remineralization and scavenging in halocline waters from the shelf. This distribution pattern of DFe is also supported by the ratio between unfiltered and dissolved Fe (high (〉4) above the shelf and low (〈4) off the shelf).

Description: Dissolved manganese (Mn) is a biologically essential element. Moreover, its oxidised form is involved in removing itself and several other trace elements from ocean waters. Here we report the longest thus far (17500 km length) full-depth ocean section of dissolved Mn in the west Atlantic Ocean, comprising 1320 data values of high accuracy. This is the GA02 transect that is part of the GEOTRACES programme, which aims to understand trace element distributions. The goal of this study is to combine these new observations with new, state-of-the-art, modelling to give a first assessment of the main sources and redistribution of Mn throughout the ocean. To this end, we simulate the distribution of dissolved Mn using a global-scale circulation model. This first model includes simple parameterisations to account for the sources, processes and sinks of Mn in the ocean. Oxidation and (photo)reduction, aggregation and settling, as well as biological uptake and remineralisation by plankton are included in the model. Our model provides, together with the observations, the following insights: – The high surface concentrations of manganese are caused by the combination of photoreduction and sources contributing to the upper ocean. The most important sources are sediments, dust, and, more locally, rivers. – Observations and model simulations suggest that surface Mn in the Atlantic Ocean moves downwards into the southward-flowing North Atlantic Deep Water (NADW), but because of strong removal rates there is no elevated concentration of Mn visible any more in the NADW south of 40° N. – The model predicts lower dissolved Mn in surface waters of the Pacific Ocean than the observed concentrations. The intense oxygen minimum zone (OMZ) in subsurface waters is deemed to be a major source of dissolved Mn also mixing upwards into surface waters, but the OMZ is not well represented by the model. Improved high-resolution simulation of the OMZ may solve this problem. – There is a mainly homogeneous background concentration of dissolved Mn of about 0.10–0.15 nM throughout most of the deep ocean. The model reproduces this by means of a threshold on particulate manganese oxides of 25 pM, suggesting that a minimal concentration of particulate Mn is needed before aggregation and removal become efficient. – The observed distinct hydrothermal signals are produced by assuming both a strong source and a strong removal of Mn near hydrothermal vents.

Description: Two CTD/water sampler systems were deployed during RV POLARSTERN cruise PS117. Both CTDs are SBE911plus from the manufacturer Seabird Scientific. The data from the AWI CTD have already been processed and are stored in Pangaea under https://doi.pangaea.de/10.1594/PANGAEA.910663 and can be downloaded there. The NIOZ-Ultra Clean CTD incl. water sampler could not be used with direct data transmission, so it was operated together with a SBE17 for control and storage of the data. At the beginning of the cruise there were problems with the setup of the SBE17 unit so that profiles were not recorded completely. After several attempts, the problem was identified in the SBE17. A replacement of this unit was shipped to Neumayer Station and brought on board POLARSTERN. After the replacement of the SBE17 the system worked reliable. However, this also meant that the failure of a conductivity sensor was only detected and replaced at a late stage. For this reason, usable CTD profiles are only available from station 36 onwards. In order to obtain a data set comparable to the AWI-CTD, profiles made with AWI-CTD and NIOZ-CTD at the same stations were used. The difference between the processed AWI-CTD and the unprocessed NIOZ-CTD is used to correct the NIOZ-CTD.

Description: We report a comprehensive dataset of dissolved iron (Fe) comprising 482 values at 22 complete vertical profiles along a 1° latitudinal section at the Zero meridian. In addition a shorter high resolution (~00°09') surface section of the southernmost part of the transect (66°00' - 69°35' S) is presented. Within the upper surface mixed layer the concentrations of dissolved Fe vary between 0.1 and 0.3 nM. An inverse trend versus fluorescence suggests significant Fe removal by plankton blooms. Vertical mixing and upwelling are the most important supply mechanisms of iron from deep waters to the upper surface mixed layer. At lower latitude (42°S) there is a distinct maximum of 0.6-0.7 nM in the 2000-3000 m depth range due to inflow of North Atlantic Deep Water. In one region (55°S) elevated dissolved Fe found in the surface mixed layer is ascribed to the recent deposition of aeolian dust originating from South America. Close to the Antarctic continent there is an indication of Fe supply in surface waters from icebergs. In the deep waters there is a strong indication of a hydrothermal plume of dissolved Fe and Mn over the ridge in the Bouvet region (52-56°S). In the Weddell Gyre basin the dissolved Fe in the deep water is 0.47±0.16 nM in the eastward flow at ~56-62°S and is lower with a value of 0.34±0.14 nM in the westward flow at high ~62-69°S latitude. At the edge of the continental ice-sheet on the prime meridian, the continental margin of the Antarctic continent appears to be lesser source of dissolved Fe than in any other place in the world; this is likely because it is unique in being overlain by the extending continental ice-sheet that largely prevents biogeochemical cycling.

Description: As part of the GEOTRACES Polarstern expedition ANT XXIV/3 (ZERO and DRAKE) we have measured the vertical distribution of 234Th on sections through the Antarctic Circumpolar Current along the zero meridian and in Drake Passage and on an EW section through the Weddell Sea. Steady state export fluxes of 234Th from the upper 100m, derived from the depletion of 234Th with respect to its parent 238U, ranged from 621±105 dpm/m**2/d to 1773±90 dpm/m**2/d. This 234Th flux was converted into an export flux of organic carbon ranging from 3.1-13.2 mmolC/m**2/d (2.1-9.0 mmolC/m**2/d) using POC/234Th ratio of bulk (respectively 〉50 µm) suspended particles at the export depth (100 m). Non-steady state fluxes assuming zero flux under ice cover were up to 23% higher. In addition, particulate and dissolved 234Th were measured underway in high resolution in the surface water with a semi-automated procedure. Particulate 234Th in surface waters is inversely correlated with light transmission and pCO2 and positively with fluorescence and optical backscatter and is interpreted as a proxy for algal biomass. High resolution underway mapping of particulate and dissolved 234Th in surface water shows clearly where trace elements are absorbed by plankton and where they are exported to depth. Quantitative determination of the export flux requires the full 234Th profile since surface depletion and export flux become decoupled through changes in wind mixed layer depth and in contribution to export from subsurface layers. In a zone of very low algal abundance (54-58 °S at the zero meridian), confirmed by satellite Chl-a data, the lowest carbon export of the ACC was observed, allowing Fe and Mn to maintain their highest surface concentrations (Klunder et al., this issue, Middag et al., this issue). An ice-edge bloom that had developed in Dec/Jan in the zone 60-65 °S as studied during the previous leg (Strass et al., in prep) had caused a high export flux at 64.5 °S when we visited the area two months later (Feb/March). The ice-edge bloom had then shifted south to 65-69 °S evident from uptake of CO2 and dissolved Fe, Mn and 234Th, without causing export yet. In this way, the parallel analysis of 234Th can help to explain the scavenging behaviour of other trace elements.