Description: Productivity regime and phytoplankton size structure are described for two different epipelagic systems in the tropical/subtropical Northeast Atlantic Ocean investigated during 9–11 day drift studies in spring 1989 in the JGOFS North Atlantic Bloom Experiment, 18°N, 30°W and 33°N, 20°W. At the 18°N study site, an oligotrophic system was encountered. The water column above the main pycnocline at about 50–60 m depth was nutrient-depleted, and both chlorophyll and primary production displayed subsurface maxima at the nutricline. Picoplankton was the dominant size fraction, accounting for 78–90% of chlorophyll and 83–98% of primary production. Synechococcus-type coccoid cyanobacteria were the dominant picoplankters. The hydrographic situation was characterized by high small-scale variability; the most interesting feature was the intrusion of nutrient-depleted Subtropical Salinity Maximum Water into the euphotic zone, whose impacts on the productivity regime are discussed. At 33°N study site, a post-bloom situation was encountered. Although the euphotic zone was nutrient-depleted, higher amounts of larger phytoplankton were present, the contribution of picoplankton being 42–53% of chlorophyll and 42–86% of primary production. Over the course of the drift study, subsurface maxima of chlorophyll and productivity evolved, the contribution of picoplankton having increased. Picocyanobacteria again were the dominant picoplankters. At both study sites the profiles of abundance ratios of picocyanobacteria to picoeucaryotes cell numbers proved to be a useful tool to characterize water masses.

Description: The productivity regime and size structure of phytoplankton are described for three different epipelagic systems in the Arabian Sea during the inter-monsoon period in spring 1987: (1) the coast of Oman; (2) the central Arabian Sea; and (3) the shelf off Pakistan. These results are related to the functioning of the specific ecosystem. Off the coast of Oman, the transition from a surface maximum of autotrophic biomass and production to a more oligotrophic system, with a chlorophyll subsurface maximum, was observed. Concomitantly, the size spectrum changed towards a higher significance of picoplankton. In the central Arabian Sea, a typical oligotrophic system with a pronounced subsurface maximum of autotrophic biomass and primary production was encountered. Here, the epipelagic system could be divided into two distinct sub-systems: the surface layer “regenerated” production, the predominance of picophytoplankton and minor losses due to sedimentation, thus a “closed” system; and the subsurface maximum layer at the nutricline characterized by higher sedimentation losses and more diatoms. Both sub-systems showed about the same productivity, the turnover in the surface layer having been much greater than in the subsurface maximum. The system on the shelf off Pakistan is seen as a decay stage of the open ocean system when water from offshore is transported onto the shelf during the onset of monsoon winds.

Description: During a R.V. Meteor JGOFS-NABE cruise to a tropical site in the northeast Atlantic in spring 1989, three different vertical regimes with respect to nitrate distribution and availability within the euphotic zone were observed. Besides dramatic variations in the depth of the nitracline, a previously undescribed nose-like nitrate maximum within the euphotic zone was the most prominent feature during this study. Both the vertical structure of phytoplankton biomass and the degree of absolute and relative new production were related to the depth of the nitracline, which in turn was dependent on the occurrence/non-occurrence of the subsurface subtropical salinity maximum (S(max)). The mesoscale variability of the nitracline depth, as indicated from a pre-survey grid, and published data on the frequent occurrence of the S(max) in tropical waters suggest higher variability of new production and F-ratio than usually expected for oligotrophic oceans. The importance of salt fingering and double diffusion for nitrate transport into the euphotic zone is discussed.

Description: Observations during a spring phytoplankton bloom in the northeast Atlantic between March and May 1992 in the Biotrans region at 47°N, 20°W, are presented. During most of the observation period there was a positive heat flux into the ocean, winds were weak, and the mixed layer depth was shallow (〈40 m). Phytoplankton growth conditions were favourable during this time. Phytoplankton biomass roughly doubled within the euphotic zone over the course of about 7 days during mid-April, and rapidly increased towards the end of the study until silicate was depleted. However, the stratification of the water column was transient, and the spring bloom development was repeatedly interrupted by gales. During two storms, in late March and late April, the mixed-layer depth increased to 250 and 175 m, respectively. After the storm events significant amounts of chlorophyll-a, particulate organic carbon and biogenic silica were found well below the euphotic zone. It is estimated that between 56% and 65% of the seasonal new production between winter and early May was exported from the euphotic zone by convective mixing, in particular, during the two storm events. Data from the NABE 47°N study during spring 1989 are re-evaluated. It is found that convective particle export was of importance during the early part of that bloom too, but negligible during the height of the bloom in May 1989. The overall impact of convective particle export during spring 1989 was equivalent to about 36% of new production. In view of these and previously published findings it is concluded that convective transport during spring is a significant process for the export of particulate matter from the euphotic zone in the temperate North Atlantic

Description: The results of an investigation of tintinnids from the western Arabian Sea are described. A total of 134 closing-net samples was obtained from 22 stations of the German "Meteor" expedition 1964/1965. Distribution charts of the dominant species of tintinnids from the study area are presented as well as a list of the world-wide distribution of these species as derived from the literature. Tintinnids were most abundant in the surface waters. The layer from 0 - 25 m yielded a maximum 94.3% and a minimum of 61.3% of the tintinnids present from 0 - 175 m; the mean was 80%. There was no significant difference in the vertical distribution between day and night stations nor was there any indication of the influence of the thermocline upon vertical distribution of tintinnids. TS-diagrams show different water types in the western Arabian Sea. Temperatur-salinity-tintinnid –diagrams indicate regional patterns in the distribution of various species of tintinnids. Some tintinnids can be used as indicator species: Climacocylis scalaria, Parundella lohmanni and Amphorella amphora were typical for the Somali Current whereas Rhabdonella apophysata and Branditella palliata indicated the presence of East African Coastal Current water. The concentration of tintinnids in the upper 25 m raged between 4,800 and 39,300 individuals/m**3 (mean 19,000/m**3). Plasma volume of tintinnids was calculated to permit comparison of different links in the food chain. There was a mean of 51 mm**3/m**2 in the upper layer, equivalent to a concentration of 2 mm**3/m**3. Carbon values were computed from the plasma volume of tintinnids, phytoplankton and larger zooplankton. The ratio of phytoplankton plus microzooplankton carbon to large zooplankton carbon was 1 : 0.8 in the Somali Current, 1 : 0.4 in the East African Coastal Current and 1 : 1.2 in the mixing zone of these current systems. Tintinnids are one of the first links in the food chain. It is very likely that a part of the organic detritus and of the nanoplankton is transfered to large herbivores or omnivores via tintinnids and other protozoans. This mechanism might be especially effective during seasons when large phytoplankters are not available in the ocean.

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: A decade of particle flux measurements providse the basis for a comparison of the eastern and western province s of the Nordic Seas. Ice-related physical and biological seasonality as well as pelagic settings jointly control fluxes in the western Polar Province which receive s southward flowing water of Polar origin. Sediment trap data from this realm highlight a predominantly physical flux control which leads to exports of siliceous particle s within the biological marginal ice zone as a prominent contributor. In the northward flowing waters of the eastern Atlanti c Province, feeding strategies, life histories and the succession ofdominant mesozooplankters (copepods and pteropods) are central in controlling fluxes. Furthermore, more calcareous matter is exported here with a shift in flux seasonality towards summer I autumn. Dominant pelagic processes modeled numerically as to their impact on annual organic carbon exports for both provinces confirm that interannual flux variability is related to changes in the respecti ve control mechanisms. Annual organic carbon export s are strikingly similar in the Polar and Atlantic Province s (2.4 and 2.9 g/m**2/y 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 (1.4 and 0.6 g/m**2/y) and carbonate (6.8 and 10.4 g/m**2/y). Interannual 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, 1000 m in 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 advectedlresuspended particles) are often juxtaposed to primary (pelagic) fluxes, a pattern which is most prominent in the Atlantic Province. Spatial variability within the Atlantic 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 seasonally 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 patterns may be differentiated and interannual variability can be analyzed in this manner to impro ve our ability to couple pelagic export patterns with benthic and geochemical sedimentary processes in seasonally ice-covered seas.