ALBERT

Description: We measured the vertical water column distribution of nitrous oxide (N2O) during the European Iron Fertilization Experiment (EIFEX) in the subpolar South Atlantic Ocean during February/March 2004 (R/V Polarstern cruise ANT XXI/3). Despite a huge build‐up and sedimentation of a phytoplankton bloom, a comparison of the N2O concentrations within the fertilized patch with concentrations measured outside the fertilized patch revealed no N2O accumulation within 33 days. This is in contrast to a previous study in the Southern Ocean, where enhanced N2O accumulation occurred in the pycnocline. Thus, we conclude that Fe fertilization does not necessarily trigger additional N2O formation and we caution that a predicted radiative offset due to a Fe‐induced additional release of oceanic N2O might be overestimated. Rapid sedimentation events during EIFEX might have hindered the build‐up of N2O and suggest, that not only the production of phytoplankton biomass but also its pathway in the water column needs to be considered if N2O radiative offset is modeled.

Description: A decade of particle flux measurements providse the basis for a comparison of the eastem and westem provinces ofthe Nordic Seas. Ice-related physical and biological seasonality as well as pelagic settings jointly control fluxes in the westem Polar Province which receives southward flowing water of Polar origin. Sediment trap data from this realm highlight a predominantly physical flux control which leads to exports of siliceous particles within the biological marginal ice zone as a prominent contributor. In the northward flowing waters of the eastem Atlantic Province, feeding Strategie . life histories and the succession of dominant mesozooplankters (copepods and pteropods) are central in controlling fluxes. Furthermore, more calcareous matter is exported here with a shift in flux seasonality towards surnrner/autumn. Dominant pelagic processes modeled numerically as to their impact on annual organic carbon exports for both provinces confirrn that interannual flux variability is related to changes in the respective control mechanisms. Annual organic carbon exports are strikingly similar in the Polar and Atlantic Provinces (2.4 and 2.9 g m-2 y-1 at 500 m depth). despite major differences in flux control. The Polar and Atlantic Provinces. however, can be distinguished according to annual fluxes of opal ( l.4 and 0.6 g m-2 y-1) and carbonate (6.8 and 10.4 g m-2 y-1). lnterannual variability may blur this in single years. Thus. it is vital to use multi-annual data sets when including particle exports in general biogeochemical province descriptions. Vertical flux profiles (collections from 500 m, l000 min both provinces and 300-600 m above the seafloor deviate from the general vertical decline of fluxes due to particle degradation during sinking. At depths 〉 1000 m secondary fluxes (laterally advected/re uspended particles) are often juxtaposed to primary (pelagic) fluxes, a pattem which is most prominent in the Atlantic Province. Spatial variability within theAtlantic Province remains poorly understood. and the same holds true for interannual variability. No proxies are at hand for this province to quantitatively relate fluxes to physical or biological pelagic properties. For the easonally ice-covered Polar Province a robust relationship exists between particle export and ambient ice-regime (Ramseier et al. this volume; Ramseier et al. 1999). Spatial flux pattems may be differentiated and interannual variability can be analyzed in this manner to improve our ability to couple pelagic export pattems with benthic and geochemical sedimentary processes in seasonally ice-covered seas.

Description: H2O2 was measured in the upper water column (0–200 m) along a west-east transect through the Equatorial Atlantic as part of the German SOLAS (Surface Ocean Lower Atmosphere) cruise Meteor 55 (M55). Vertical profiles of H2O2 showed characteristic exponential decay consistent with light profiles and rainwater inputs. Integrated (0–100 m) water column H2O2 inventories ranged from 1.1–8.9 mmol m−2 with the highest values in the Amazon Plume. H2O2 inventories were also higher at the Equatorial Upwelling and after heavy rain showers in the region of the Inter Tropical Convergence Zone (ITCZ). Analysis of rain water samples collected during the cruise gave a volume weighted mean of 10.8 μmol L−1 (range 1.5–22.3 μmol L−1). This work highlights the importance of rainwater as a major source for H2O2 in the surface waters under the ITCZ.

Description: The effect of combined iron, silicate, and light co-limitation was investigated in the three diatom species Actinocyclus sp. Ehrenberg, Chaetoceros dichaeta Ehrenberg, and Chaetoceros debilis Cleve, isolated from the Southern Ocean (SO). Growth of all species was co-limited by iron and silicate, reflected in a significant increase in the number of cell divisions compared to the control. Lowest relative Si uptake and drastic frustule malformation was found under iron and silicate co-limitation in C. dichaeta, while Si limitation in general caused cell elongation in both Chaetoceros species. Higher light intensities similar to SO surface conditions showed a negative impact on growth of C. dichaeta and Actinocyclus sp. and no effect on C. debilis. This is in contrast to the assumed light limitation of SO diatoms due to deep wind driven mixing. Our results suggest that growth and species composition of Southern Ocean diatoms is influenced by a sensitive interaction of the abiotic factors, iron, silicate, and light.

Description: Pelagic processes and their relation to vertical flux have been studied in the Norwegian and Greenland Seas since 1986. Results of long-term sediment trap deployments and adjoining process studies are presented, and the underlying methodological and conceptional background is discussed. Recent extension of these investigations at the Barents Sea continental slope are also presented. With similar conditions of input irradiation and nutrient conditions, the Norwegian and Greenland Seas exhibit comparable mean annual rates of new and total production. Major differences can be found between these regions, however, in the hydrographic conditions constraining primary production and in the composition and seasonal development of the plankton. This is reflected in differences in the temporal patterns of vertical particle flux in relation to new production in the euphotic zone, the composition of particles exported and in different processes leading to their modification in the mid-water layers. In the Norwegian Sea heavy grazing pressure during early spring retards the accumulation of phytoplankton stocks and thus a mass sedimentation of diatoms that is often associated with spring blooms. This, in conjunction with the further seasonal development of zooplankton populations, serves to delay the annual peak in sedimentation to summer or autumn. Carbonate sedimentation in the Norwegian Sea, however, is significantly higher than in the Greenland Sea, where physical factors exert a greater control on phytoplankton development and the sedimentation of opal is of greater importance. In addition to these comparative long-term studies a case study has been carried out at the continental slope of the Barents Sea, where an emphasis was laid on the influence of resuspension and across-slope lateral transport with an analysis of suspended and sedimented material.

Description: Nitrogen fixation supports new production in the oligotrophic oceans and removes dinitrogen and carbon dioxide from mixed layer waters. N‐fixation rates have been estimated in various ways but measurements are still too rare and factors limiting N‐fixation are not yet fully understood. Here we present data from a transect along 10°N through the tropical Atlantic on the Meteor Cruise 55 where N‐fixation rates between 3.7 and 255 μmol N*m−2*d−1 were recorded. The highest rates occurred off Africa in the eastern tropical North Atlantic (ETNA), and in the Amazon River plume in the West and contributed to 1–12.2% of the N‐demand of primary production. N‐fixation rates correlated with dissolved Fe concentrations, which were 20–280 times greater than the estimated demand. High atmospheric Fe inputs combined with the shallow nutricline make the ETNA a favourable environment for N‐fixers.

Description: The tropical oceans are a source of reactive bromine to the atmosphere in the form of short-lived brominated methanes as bromoform (CHBr3) and dibromomethane (CH2Br2). Elevated atmospheric concentrations above the tropical oceans are related to oceanic supersaturations of the compounds and especially to upwelling regimes. Although the sources of these brominated gases in the open ocean are not well understood, they have been habitually linked to phytoplankton, especially diatom abundance. Thus according to common assumptions, high concentrations of the brominated trace gases were expected to occur in the biologically active and diatom-rich Mauritanian upwelling. However, contrary to expectations, only low levels were encountered in the upwelling waters, 10.7 (range 5.2–23.8) pmol L−1 CHBr3 and 4.7 (range 3.1–7.0) pmol L−1 CH2Br2, values more typical of open ocean concentrations. The aqueous CHBr3 concentrations were not correlated to high chlorophyll a values or diatom abundances. However, significant correlations existed with low concentrations of marker pigments for diatoms, cyanobacteria, and degradation, suggesting miscellaneous small biological sources of the compound in the upwelling. Air-sea exchange could additionally account for an oceanic source in fresh upwelled waters, while advection of different water masses also influenced the distribution. CHBr3 concentrations were maximized in warm and nitrogen-depleted surface waters, while CH2Br2 was maximized in colder and nitrogen-enriched deeper waters, suggesting that both compounds, at least in part, have different sources and fates.