Description: The relationship between physical properties of the water column and spatial patchiness of phytoplankton spring bloom development on the Greenland shelf edge and in the Irminger Sea was investigated using data collected during a spring cruise (April and May 2002). The observations confirm a strong relationship between the onset and stage of bloom development and the stratification induced by freshwater input to the surface layer in the shelf region. Interestingly, at the shelf, in the region influenced by melting of the seasonal ice-cover, the vertical distribution of chlorophyll a showed a subsurface maximum at ca. 25 m depth at several stations. Since nutrients were not exhausted at these stations, such a pattern does not conform to the general picture of a spring bloom. In contrast, in the open ocean part of the Irminger Sea pre-bloom conditions and a retarded development of the phytoplankton population were observed with low, more uniform distribution of chlorophyll a. The nitrate drawdown was estimated at between 16.5 and 270 µm m–2 (mean 108.6 ± 82.2 µm m–2) and the new primary production was estimated to be between 1.3 and 21.4 g C m–2 (8.6 ± 6.5 g C m–2), corresponding to 0.42 g C m–2 d–1. The phytoplankton community in the melting ice zone consisted of Phaeocystis sp., small flagellates (〈 4 µm) and picoplankton, while diatoms were less abundant. Phaeocystis sp. contributed up to 15 g C m–2 to the carbon biomass (70% of total carbon measured), whereas the contribution of diatoms and flagellates to carbon biomass was relatively low, with up to 1.2 g C m–2 (5.7%) and up to 2.5 g C m–2 (11.7%), respectively. On the shelf the bloom starts at the very beginning of stabilisation (elevated N2 values) which results solely from the release of meltwater. The locally restricted water stability leads to a patchy phytoplankton distribution in the Irminger Sea.

Description: Long-term observations of the deep ocean particle flux from three sites in the northeast Atlantic (33 degrees N, 22 degrees W; 47 degrees N, 20 degrees W; 54 degrees N, 20 degrees W) provide the basis for comparison and characterization of the biogeochemical provinces in terms of sedimentation pattern. Deep ocean particle flux data (2000 in) for fluxes of total mass and the flux composition are presented and compared to published sediment trap data from this area to consider regional-scale variations in the quantity and composition of settling material. The observations show that in the northeast Atlantic gradient of decreasing mass flux from North to South, exists consistent with known changes of biological productivity in surface waters. This gradient is associated with similar trends in opal and particulate organic carbon, whereas calcium carbonate shows trend in the opposite direction. The changes in the composition of the settling material found along the transect are indicating that the calcium carbonate flux is critical in removing organic matter from the upper ocean to the deeper sink. Its role declines from the subtropical ocean (60-80% of the particle flux) towards North (〈 40%) reflecting the decreasing importance of coccolithophorid/foraminiferal blooms for particle flux from the subtropical to the subpolar North Atlantic. In contrast, the role of biogenic silica (opal) in regard to the ballasting effect increases towards North. The northern sites have much higher percentage of biogenic silica than the sites in the South, because of the deep winter mixing and the seasonality of phytoplankton dominated by diatom blooms during spring and summer. The comparison of the seasonal pattern of particle flux with the seasonal pattern of surface chlorophyll a concentrations from SeaWiFS together with the similarity of the pattern observed in calcium carbonate and opal leads to the conclusion that the particle flux at two positions (33 degrees N, 22 degrees W; 47 degrees N, 20 degrees W) is fast and directly coupled to the phytoplankton dynamics in the overlying euphotic zone.

Description: Analysis of the demographic structure of Calanus species in the North Atlantic presents particular difficulties due to the overlapping spatial distributions of four main congeneric species (Calanus finmarchicus, Calanus helgolandicus, Calanus glacialis and Calanus hyperboreus). These species have similar morphologies, making microscopic discrimination only possible between some of the species at late copepodite or adult stages. However, molecular techniques now offer the possibility of screening significant numbers of specimens and unambiguously identifying them to species, regardless of developmental stage. Unfortunately, the processing rate of specimens by molecular methods is still too low to offer a realistic alternative to microscopy for analysis of samples from large field surveys. Here, we outline and test an approach involving the use of molecular methodology in conjunction with conventional microscopy to assess the species assignment of developmental stage abundances of Calanus congeners. Our study has highlighted many important methodological issues. First, it cannot be assumed that the species composition is homogeneous across the development stages; applying proportional species composition of adults to morphologically undistinguishable earlier development stages can result in error. The second important conclusion is that prosome length may be a highly unreliable discriminator of C. finmarchicus and C. glacialis

Description: Analysis of the demographic structure of Calanus species in the North Atlantic presents particular difficulties due to the overlapping spatial distributions of four main congeneric species (Calanus finmarchicus, Calanus helgolandicus, Calanus glacialis and Calanus hyperboreus). These species have similar morphologies, making microscopic discrimination only possible between some of the species at late copepodite or adult stages. However, molecular techniques now offer the possibility of screening significant numbers of specimens and unambiguously identifying them to species, regardless of developmental stage. Unfortunately, the processing rate of specimens by molecular methods is still too low to offer a realistic alternative to microscopy for analysis of samples from large field surveys. Here, we outline and test an approach involving the use of molecular methodology in conjunction with conventional microscopy to assess the species assignment of developmental stage abundances of Calanus congeners. Our study has highlighted many important methodological issues. First, it cannot be assumed that the species composition is homogeneous across the development stages; applying proportional species composition of adults to morphologically undistinguishable earlier development stages can result in error. The second important conclusion is that prosome length may be a highly unreliable discriminator of C. finmarchicus and C. glacialis.