Fluxes of dissolved aluminum and manganese to the Weddell Sea and indications for manganese co-limitation

<p>The trace metals aluminum (Al) and manganese (Mn) were studied in the Weddell Sea in March 2008. Concentrations of dissolved Al ([Al]) were slightly elevated (0.23-0.35 nmol L-1) in the surface layer compared to the subsurface minimum (0.07-0.21 nmol L-1) observed in the winter water. Atmospheric deposition is the main source of Al to the central Weddell Sea (22 mu mol m(-2) yr(-1)), and the residence time of dissolved Al in the upper mixed layer is similar to 0.8 yr. The flux from the shelf and slope regions equals about 50% of the atmospheric input of Al to the western Weddell Sea. The highest [Al] in the Weddell Sea bottom water (WSBW) is related to the formation of deep water, and the associated downward flux is in the range of 3-10 mu mol Al m(-2) yr(-1). The concentrations of dissolved Mn ([Mn]) were depleted in the surface layer, likely as a result of biological uptake, as indicated by the correlation among Mn, major nutrients, and fluorescence. The significant negative relation between the Delta Mn:Delta P ratio and the ambient concentration of dissolved iron indicates iron-Mn co-limitation. The flux of Mn from the continental margin is about 2.2 times greater than atmospheric input (1.1 mu mol m(-2) yr(-1)). The flux of both Al and Mn from the continental margin indicates melting of continental ice (icebergs) or direct continental runoff. The slightly elevated [Mn] in the WSBW is due to a relatively small flux of 1 mu mol Mn m(-2) yr(-1) associated with WSBW formation.</p>

Dissolved iron measured on water bottle samples during POLARSTERN cruise ANT-XXIV/3

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

Average fluorescence and dissolved iron and Fe-binding ligand characteristics during POLARSTERN expedition ANT-XXIV/3 in 2008

Organic complexation of dissolved iron (dFe) was investigated in the Atlantic sector of the Southern Ocean in order to understand the distribution of Fe over the whole water column. The total concentration of dissolved organic ligands ([Lt]) measured by voltammetry ranged between 0.54 and 1.84 nEq of M Fe whereas the conditional binding strength (K') ranged between 10**21.4 and 10**22.8. For the first time, trends in Fe-organic complexation were observed in an ocean basin by examining the ratio ([Lt]/[dFe]), defined as the organic ligand concentration divided by the dissolved Fe concentration. The [Lt]/[dFe] ratio indicates the saturation state of the natural ligands with Fe; a ratio near 1 means saturation of the ligands leading to precipitation of Fe. Reversely, high ratios mean Fe depletion and show a high potential for Fe solubilisation. In surface waters where phytoplankton is present low dissolved Fe and high variable ligand concentrations were found. Here the [Lt]/[dFe] ratio was on average 4.4. It was especially high (5.6-26.7) in the HNLC (High Nutrient, Low Chlorophyll) regions, where Fe was depleted. The [Lt]/[dFe] ratio decreased with depth due to increasing dissolved Fe concentrations and became constant below 450 m, indicating a steady state between ligand and Fe. Relatively low [Lt]/[dFe] ratios (between 1.1 and 2.7) existed in deep water north of the Southern Boundary, facilitating Fe precipitation. The [Lt]/[dFe] ratio increased southwards from the Southern Boundary on the Zero Meridian and from east to west in the Weddell Gyre due to changes both in ligand characteristics and in dissolved iron concentration. High [Lt]/[dFe] ratio expresses Fe depletion versus ligand production in the surface. The decrease with depth reflects the increase of [dFe] which favours scavenging and (co-) precipitation, whereas a horizontal increase in the deep waters results from an increasing distance from Fe sources. This increase in the [Lt]/[dFe] ratio at depth shows the very resistant nature of the dissolved organic ligands

Dissolved iron measurements from 44 stations in the shallow Arctic Ocean waters and Shelf Sea's during POLARSTERN cruise ARK-XXII/2

Concentrations of dissolved (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 (R**2 = 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 (4) above the shelf and low (<4) off the shelf)

Radionuclides measured on 27 water bottle profiles during POLARSTERN cruise ANT-XXIV/3

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