ALBERT

Description: A synopsis of results from two sediment trap moorings deployed at the mid- and outer slope (water depths 1450 and 3660 m, respectively) of the Goban Spur (N.E. Atlantic Margin) is presented. Fluxes increase with trap deployment depth; below 1000 m resuspended and advected material contributes increasingly to bulk flux. Fluxes of dry weight, POC and diatoms in the traps 400 m above bottom (mab) are smaller than those recorded at the sediment surface due to lateral fluxes in the benthic nepheloid layer. These near-bottom fluxes are larger at shallower water depths. 231Pa/230Th ratios in sedimenting material suggest that boundary scavenging is not significant at the Goban Spur. Fluxes of 210Pb in the intermediate and deep traps are comparable to the 210Pb supply rate at this site. At the outer slope, sediment 210Pb fluxes are similar to those measured in the traps 400 mab; at the mid-slope they are a factor of 2 higher, once again indicating large near-bottom lateral particle input. Based on POC-normalised biomarkers in sedimenting material, we followed changes in the quality of sedimenting material with differing trap depth and on seasonal and event-related time scales. In spring fresh, diatom-dominated sedimentation occurs, with progressive degradation of POC with time (to winter) and depth (from 600 to 3220 m). Deeper traps are distinguished on the basis of opal and aluminium fluxes that are dominant in lateral input. A storm event during late September 1993 was clearly reflected in the δ15N isotope ratio of sedimenting material, with a time lag of 2–3 weeks. Diatom and opal fluxes were elevated in this storm-related signal, and its biomarker composition in the 600-m trap was similar to that during spring. An estimate made of upward nitrate flux (new production) at the shelf break and at the outer slope indicated a 2-fold higher new (export) production at the shelf break. Particulate organic carbon export from the shelf break to below the depth of maximal seasonal mixing ranges between 3 and 9% of primary production.

Description: In the framework of the Ocean Margin Exchange project, a multi-disciplinary study has been conducted at the shelf edge and slope of the Goban Spur in order to determine the spatial distribution, quantity and quality of particle flux, and delineate the transport mechanisms of the major organic and inorganic components. We present here a synthesis view of the major transport modes of both biogenic and lithogenic material being delivered to the open slope of the Goban Spur. We attempt to differentiate between the direct biogenic flux from the surface mixed layer and the advective component, both biogenic and lithogenic. Long-term moorings, instrumented with sediment traps, current meters and transmissometers have yielded samples and near-continuous recordings of hydrographic variables (current direction and speed, temperature and salinity) and light transmission for a period of 2.5 years. Numerous stations have been occupied for CTD casts with light transmission and collection of water samples. The sedimenting material has been analysed for a variety of marker compounds including phytoplankton pigments, isotopic, biomineral and trace metal composition and microscopical analyses. These samples are augmented by seasonal information on the distribution and composition of fine particles and marine snow in the water column. The slope shows well-developed bottom nepheloid layers always present and intermediate nepheloid layers intermittently present. Concentrations are mainly in the range 50–130 mg m−3 in nepheloid layers and 6–25 mg m−3 in clear water. A seasonal variability in the concentration at the clear water minimum is argued to be related to seasonal variations in vertical flux and aggregate break-up in transit during summer months. It is suggested that the winter sink for this seasonal change in particulate matter involves some re-aggregation and scavenging, and some conversion of particulate to dissolved organic matter. This may provide a slow seasonal pump of dissolved organic carbon to the deep ocean interior. Differences in trapped quantities at different water depths are interpreted as due to lateral flux from the continental margin. There is a major lateral input between 600 and 1050 m at an inner station and between 600 and 1440 m at an outer one. The transport is thought to be related to intermediate nepheloid layers, but those measured are too dilute to be able to supply the flux. Observed bottom nepheloid layers are highly concentrated very close to the bed (up to 5 g m−3), with a population of large aggregates. Some of these are capable of delivering the flux seen offshore during intermittent detachment of nepheloid layers into mid-water. Concentrated bottom nepheloid layers are also able to deliver large particles with unstable phytoplankton pigments to the deep sea floor in a few tens of days. Calculated CaCO3 fluxes are adjusted for dissolution, which is inferred from Ca/Al ratios to be occurring in the CaCO3-saturated upper water column where up to 80% of the CaCO3 resulting from primary production is dissolved.

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: Taxon-specific microzooplankton dynamics were studied along a transect through the North Atlantic Drift from 70°N 04°E to 40°N 20°W during July 1997 using serial dilution and nutrient-enrichment experiments. Nutrient concentrations and microzooplankton composition indicated postbloom conditions at 40°N, 47°N, and 50°N, a transitional system at 54°N, and bloom conditions at 62°N and 70°N. The ratio of microzooplankton to phytoplankton biomass was inversely related to nitrate and phosphate concentrations. Potential grazing thresholds were observed in four of nine experiments at 40–66% of the initial phytoplankton concentration. Grazing losses were determined for six pigment-specific classes of phytoplankton. Selective grazing losses of phytoplankton taxa ranged from 73% to 248% of the nonselective grazing losses predicted according to their biomass contributions. The grazing selectivity varied considerably between communities, with the microherbivores showing positive selection for cyanobacteria and dinoflagellates and predominantly avoidance of chlorophyta and bacillariophyceae. Microzooplankton did not show a preference for the dominant phytoplankton taxa, but grazed preferentially on fast-growing phytoplankton with minor contributions (〈15%) to the phytoplankton biomass. However, bacillariophyceae were the major contributors to phytoplankton biomass and accounted for major fractions of the total losses through microzooplankton grazing. Microzooplankton consumed the equivalent of 0.12–5.5 times their own biomass daily on a carbon basis, amounting to 65–197% of gross phytoplankton production. With the conservative assumption that 20% of the consumed phytoplankton was converted to microzooplankton biomass, the latter was estimated to contribute 27–381% to the net production of the entire microzooplankton community. We therefore conclude that the taxonomic structure and the net production of the microzooplankton communities were significantly affected by the intensity and selectivity of herbivorous microzooplankton grazing.

Description: Barium (Ba), aluminium (Al), and zirconium (Zr) were measured in sediment trap material deployed at two margin settings of the NE Atlantic: the Bay of Biscaye at Goban Spur and the NW Iberian Margin. The Particulate Organic Carbon (POC)/Ba ratios of the trapped material in both margin environments are clearly higher compared to the open ocean. Although lateral advection of POC may partly explain these higher POC/Ba ratios for margin systems, it is clear that the yield of authigenic particulate Ba during organic matter degradation in the water column is lower in margin environments. In order to assess export production in margin settings we optimised transfer functions based on trapped Ba fluxes that were originally elaborated for open ocean settings. Calculations of export production based on trapped Ba flux and POC/Ba ratio were compared with calculations based on trapped POC flux only. Export production based on Ba flux show greater internal consistency amongst traps along the same mooring, suggesting that this approach has advantages over the one based on POC flux only. Estimated export productions are of the same order of magnitude as estimates of new production, but systematically fall short of the latter. This systematic discrepancy needs further investigation.