Notes: Summary Phyto- and protozooplankton were sampled in the upper 10 m of the water column in austral summer during a cruise of RV Polarstern from January 6 to February 20 1985 in the eastern Bransfield Strait vicinity and in the northern, southeastern (off Vestkapp, twice: I and II) and southern Weddell Sea (Vahsel Bay across the Filchner Depression to Gould Bay). The plankton assemblages are discussed in relation to physical, chemical and biological factors in the different geographical areas in summer. Phytoplankton biomass (Phytoplankton carbon, PPC) ranged from 4–194 μg carbon/l and consisted on average of 65% diatoms and 35% autotrophic flagellates. Whereas in the northwest phytoplankton assemblages were dominated by small nanoflagellates (78% of PPC), higher biomass of diatoms (54–94% of PPC) occurred at the other sampling sites. In general autotrophic flagellates and small pennate diatoms dominated at oceanic stations; in neritic areas large centric diatoms prevailed. Chlorophyll a concentrations ranged from 0.25–3.14/μg chl a/l with a mean of 1.13/gmg chlorophyll a/l and an average phytoplankton carbon/chlorophyll a ratio of 39. Protozooplankton biomass (Protozooplankton carbon, PZC) ranged from 0–67 μg carbon/l and consisted of 49% ciliates, 49% heterotrophic dinoflagellates and 2% tintinnids. Heterotrophic dinoflagellates were more important in the northern investigation areas (58%–84% of PZC). Ciliates dominated the protozooplankton in the southeast and south (56%–65% of PZC); higher abundances of tintinnids were observed only in the south (11% of PZC). The most remarkable feature of the surface waters was the high protozooplankton biomass: protozooplankton amounted to 25% on an average of the combined biomass of PPC plus PZC for the entire investigation period. Protozoan biomass in the southeastern and southern Weddell Sea occasionally exceeded phytoplankton biomass. Temperature, salinity, and inorganic nutrients were generally lower in the southern regions; at most of these stations a meltwater layer occurred in the upper meters of the water column. We suggest that this physical regime allows a well developed summer system with a high proportion of heterotrophic microplankton. In the eastern Bransfield Strait, in the northern Weddell Sea and close to the coast off Vestkapp (I), however, early summer conditions occurred with less protozooplankton contribution.

Notes: Abstract  The development of the phytoplankton bloom and its relation to water column stabilisation during the transition from early to high summer (of 1991) in the seasonally ice-covered zone of the Barents Sea were studied from a meridional transect of repeated hydrographic/biological stations. The water column stabilisation is described in detail with the aid of vertical profiles of the Brunt-Väisälä frequency squared (N2). The contributions of seasonal warming and ice melting to stabilisation are elucidated by determining the effects of temperature and salinity on N2. The spring bloom in 1991 migrated poleward from June to July by about 400 km, associated with the retreat of the ice edge. The spring bloom culminated with maximum chlorophyll concentrations in the mixed layer about 100–300 km north of the centre of the meltwater lens, at its northern edge, where the ice cover was still substantial. From the distribution of N2 it becomes obvious that the bloom starts at the very beginning of stabilisation, which results solely from the release of meltwater. The increase in temperature due to the seasonal warming does not contribute to the onset of vernal blooming; temperature starts to contribute to the stratification later, when the spring bloom has ceased due to the exhaustion of nutrients in the mixed layer. By that time a deep chlorophyll maximum has formed in the seasonal pycnocline, 20–30 m below the base of the mixed layer. The effect of the seasonal ice cover on the mean areal new primary production is discussed.