ALBERT

Description: Organic material entering the oceanic mesopelagic zone may either reenter the euphotic zone or settle into deeper waters. Therefore it is important to know about mechanisms and efficiency of substrate conversion in this water layer. Bacterial biomass, bacteria secondary production (BSP). extra­cellular peptidase activity (EPA) and particulate organic nitrogen (PON) were measured in vertical pro­files of the North Atlantic (46° N 18° W; 57° N 23° W) during the Joint Global Ocean Flux Study (JGOFS) cruise in May 1989. The magnitude of these parameters decreased differently with depth. The strong­est decreases were observed for bacterial production (3H-thymidine incorporation) and peptide turn­over (using the substrate analog leucine-methylcoumarinylamide). Bacterial biomass and peptidase potential activity were not reduced as much in the mesopelagic zone. Peptidase potential per unit cell biomass of mesopelagic bacteria was 2 to 3 times higher than that of bacteria in surface water. Nevertheless bacterial growth at depth was slow, due to slow actual hydrolysis. Values of theoretical PON hydrolysis were calculated from PON measurements and protein hydrolysis rates. These corre­sponded well to bacterial production rates, and the degree of correspondence increased from a factor of 0.63 (PON hydrolysis/ESP) in the mixed surface layer to 0.87 in the mesopelagic zone. Thus we hypothesized an effective coupling between particle hydrolysis and uptake of hydrolysate by bacteria, which depletes the deeper water of easily degradable substrates as hydrolysates usually are. The low enzymatic PON turnover rate of 0.04 d- 1 in the subeuphotic zone suggests that residence time of parti­cles within a depth stratum may be important for its contribution to export. storage and recycling of organic matter.

Description: Phosphatase (P-ase) activity was determined together with other extracellular enzyme activities, bacterial abundance and production rates during the 2 SW Monsoon process studies of the German JGOFS Arabian Sea Program. Water samples were collected along the cruise tracks from the equator to the upwelling region at the shelf edge off Oman. Depth profiles of P-ase activity were strikingly different from those of the other enzymes. While values of aminopeptidase and β-glucosidase generally decreased below the euphotic zone, P-ase increased by factors of 1 to 7. The relation between peptidase- and P-ase activity was from 4 to 21 at the surface and from 3 to 5 at 800 m depth. Because P-ase production (dissolved and cell-bound) in deep waters is mainly dependent on bacteria, P-ase activities per bacterial cell were calculated: these were, on average, 37 times higher at 800 m than at the surface. We also observed a positive correlation of P-ase activity with phosphate concentrations in the depth profiles below the euphotic zone, while this relationship was much more variable in the mixed surface layer. These observations suggest that C-limited bacteria in the deep strata did not primarily focus on the phosphate generated by their P-ase activity but on the organic C compounds which were simultaneously produced and which could probably not be taken up prior to the hydrolytic detachment of phosphate. It is hypothesised that a considerable part of the measured P-ase activity was dissolved (though it might have originated from bacteria). These enzymes may be important for the slow, but steady regeneration of phosphate and organic C in mesopelagic waters.

Description: This study deals with large spatial scale differences in the ratios between bacterial leucine incorporation (TLi: protein synthesis) and thymidine incorporation (TTi: DNA synthesis) in oligotrophic offshore and comparatively more mesotrophic inshore (sub)tropical regions of the Atlantic Ocean. Observations were derived from 2 RV ‘Polarstern’ cruises, one of which traversed a meridional mid-ocean transect while the other followed the African coast line. Average values (from 42°N to 35°S) of TLi, TTi and chlorophyll a (chl a) concentration were 40.3 pmol leucine l–1 h–1, 1.32 pmol thymidine l–1 h–1 and 0.18 µg chl a l–1 along the offshore transect, compared to 51.8 pmol leucine l–1 h–1, 2.72 pmol thymidine l–1 h–1 and 0.29 µg chl a l–1 along the inshore transect. Mean values of the TLi:TTi ratio (which defines bacterial growth characteristics) were 32.4 in offshore waters and 20.5 in inshore waters. Offshore ratios of TLi:chl a or TTi:chl a (proxy for bacterial substrate) were 274.1 and 8.5, compared to inshore ratios of 198.7 and 10.0, respectively. This means that, per unit of chl a, considerably higher bacterial protein synthesis was supported in water farther from the coast than near the coast, whereas bacterial DNA synthesis per unit chl a was slightly higher in the latter. Because temperature variability along the cruise tracts was rather similar (except in the Benguela upwelling region), we assume that substrate supply was mainly responsible for the observed significant differences in bacterial growth characteristics. In addition, the potential different contributions of picocyanobacteria to leucine uptake (TLi) must be considered. We conclude that the different TLi:TTi ratios in (sub)tropical offshore and inshore waters reflect reactions of the relevant bacterial communities to prevailing environmental conditions. Therefore, we did not interpret our results in the context of the currently used terms ‘balanced’ or ‘unbalanced’ growth. Bacterial community growth may be balanced in both regions of study, but at different levels of the TLi:TTi ratio.

Description: The response of the phytoplankton and bacterial spring succession to the predicted warming of sea surface temperature in temperate climate zones during winter was studied using an indoor-mesocosm approach. The mesocosms were filled with winter water from the Kiel Fjord, Baltic Sea. Two of them were started at ~2°C and the temperature was subsequently increased according to the decadal temperature profile of the fjord (ΔT 0°C, baseline treatment). The other mesocosms were run at 3 elevated temperatures with differences of ΔT +2, +4 and +6°C. All mesocosms were exposed to the same light conditions. Timing of peak phytoplankton primary production (PP) during the experimental spring bloom was not significantly influenced by increasing temperatures, whereas the peak of bacterial secondary production (BSP) was accelerated by about 2 d per °C. This suggests that, in case of warming, the spring peak of bacterial degradation of organic matter (in terms of BSP) would occur earlier in the year. Furthermore, the lag time between the peaks of PP and BSP (about 16 d for ΔT 0°C) would diminish progressively at elevated temperatures. The average ratio between BSP and PP increased significantly from 0.37 in the coldest mesocosms to 0.63 in the warmest ones. Community respiration and the contribution of picoplankton (〈3 µm fraction) to this also increased at elevated temperatures. Our results lead to the prediction that climate warming during the winter/ early spring in temperate climate zones will favor bacterial degradation of organic matter by tightening the coupling between phytoplankton and bacteria. However, if PP is reduced by warming, as in our experiments, this will not necessarily lead to increased recycling of organic matter (and CO2).

Description: The responses of natural bacterial populations in the waters of the Kiel Fjord, Germany, and in Lake Kinneret, Israel, to additions of organic substrates were followed by determining changes over 24 h either in direct cell counts or in 3H-thymidine incorporation, and in the Kiel Fjord additionally in 3H-leucine incorporation. In parallel, 1 ym filtered water samples were stored for 3 or 4 d in order to starve the indigenous bacterial populations prior to repeating the substrate addition experiments. Generally, upon substrate addition, relatively higher incorporation of radiotracers was noted in the preincubated samples. Growth response to substrate addition even in starved populations was only significant after 24 h. Incorporation rates of 3H-thymidine and 3H-leucine were more sensitive indicators of bacterial response to substrate additions than cell counts. Continued cell replication in unsupplemented controls, and insignificant increase over time of radiotracer incorporation in most of the fresh samples with added supplements, indicated that the indigenous bacterial populations in Kiel Fjord and Kinneret were apparently not substrate limited. Comparison of actual bacterial production after 24 h (direct counts) to that predicted by 3H-thymidine incorporation after 1 h showed that although reasonably good predictions of daily production were obtained in the unsupplemented samples, this was usually not the case when substrates were added.