ALBERT

Description: Oithona similis is an abundant but poorly studied cyclopoid copepod in the brackish Central Baltic Sea. We describe the spatio-temporal distribution of O. similis in a Central Baltic deep basin (Bornholm Basin) during spring and summer 1999. Using vertically resolving sampling in parallel with hydrographic measurements, we found the copepod to dwell in the permanent halocline characteristic of a Central Baltic deep basin. The habitat of O. similis is thus limited from above by low salinity and from below by low oxygen conditions, both characteristic for the area. Horizontally resolving sampling yielded abundance surfaces which were compared by analysis of variance showing similar patterns among sampling dates. Comparison with flow fields from a three-dimensional hydrodynamic model suggests that the horizontal distribution is primarily the result of circulation in the dwelling depth. The study shows how the physical environment in the area determines the spatial distribution which might affect abundance and production of this copepod.

Description: The seasonal development of bacteria was studied in the hypertrophic coastal lagoon Ciénaga Grande de Santa Marta (Caribbean coast of Colombia). This large but only 1.5 m deep lagoon is subject to strong seasonal variations of salinity from almost fully marine (April/May) to brackish conditions in October/November. Chlorophyll ranged from 6 to 182 μg L−1, and gross primary production amounted to 1690 g C m−2 per year. Total bacterial number (TBN) ranged from 6.5 to 90.5 × 109 cells L−1 and bacterial biomass (BBM) from 77 to 1542 μg C L−1, which are among the highest ever reported for natural coastal waters. Neither TBN nor BBM varied significantly with salinity, phytoplankton or seston concentrations. Only the bacterial mean cell volume showed a significant relation to salinity, being highest (0.066 μm3) during the period of increasing and lowest (0.032 μm3) during decreasing salinity. Bacterial protein accounted for 24% (19–26%) and phytoplankton protein for 57% (53–71%) of total seston protein. The ratio (annual mean) of bacterial carbon to phytoplankton carbon was 0.44 (range 0.04–1.43). At low phytoplankton abundance [chlorophyll a (Chl a) 〈 25 μg L−1], bacterial carbon was almost equal to phytoplankton biomass (i.e. the mean ratio was 1.04). In contrast, at Chl a 〉 100 μg L−1, BBM was low compared to phytoplankton biomass (the mean ratio was 0.16). In general, BBM varied less than phytoplankton biomass. Most probably, the missing correlation between bacterial and phytoplankton variables was due to (i) organic material partly derived from allochthonous sources serving as food resource for bacteria and (ii) a strong resuspension of bacteria from the sediment caused by frequent wind-induced mixing of the very shallow lagoon.

Description: The so-called ‘turbulence incubator’ overcomes an essential disadvantage of static in situ incubations where at high irradiances an artificial photoinhibition is caused by neglecting turbulent mixing in the upper water column. It is operated on deck and simulates the changing light conditions for vertically mixed phytoplankton cells by moving the sample bottles horizontally through a circular water bath covered by a glass lid of neutral optical density filters. In this way the exponentially decreasing irradiance within the euphotic zone is simulated and photoinhibition near the surface is avoided. A crucial point is the choice of revolution rate for simulating turbulent mixing under natural conditions. The incubator is characterized by its handy size, a relatively simple and inexpensive construction and a battery-driven motor. It can thus even be operated on small vessels without an electric generator. The incubator is especially suited for vertically mixed waters such as shallow bays, tidal estuaries and rivers. Its reliability was successfully tested by a simultaneous comparison with in situ measurements at various stations representing different water types and environmental conditions, ranging from the turbid River Elbe to the clear open Baltic Sea. In 9 out of 11 experiments, higher primary production rates were obtained in the turbulence incubator than in static in situ incubations. The majority of the latter were characterized by a pronounced photoinhibition in the upper two incubation depths representing the 100 and 50% light levels. The average rate increase amounted to 22%, with a range between 11 and 53% depending on light attenuation and irradiance.

Description: The vertical distribution patterns of paralarvae from several abundant cephalopod taxa were examined from depth-stratified tows in the northeast Pacific (44–56°N, 145–165°W) during three summer surveys in 1999–2001. A total of 309 cephalopods representing 10 taxa in three families were collected. Gonatid squids composed 97% of the total catch, and the most numerous taxa were Berryteuthis anonychus (59% of the total catch), Gonatus spp. (21%) and Gonatopsis borealis (17%). B. anonychus and Gonatus spp. were both most abundant in the upper 20 m; catches of both taxa varied significantly with depth and were significantly higher above the thermocline than in and below the thermocline. Gonatopsis borealis was collected mostly between 20 and 50 m, and catches were significantly higher in the thermocline than above and below the thermocline. Paralarvae of the three major taxa showed no evidence of diel vertical migration. Mantle lengths of Gonatus spp. and G. borealis each varied significantly with depth, and Gonatus spp. showed a strong positive correlation between mantle length and depth.

Description: Selectivity-size spectra, clearance and ingestion rates and assimilation efficiencies of Acartia clausi (Copepoda), Penilia avirostris (Cladocera) and Doliolum denticulatum (Doliolida) from Blanes Bay (Catalan Sea, NW Mediterranean) were evaluated in grazing experiments over a wide range of food concentrations (0.02–8.8 mm3 L−1 plankton assemblages from Blanes Bay, grown in mesocosms at different nutrient levels). Acartia clausi reached the highest grazing coefficients for large algae 〉70 μm (longest linear extension), P. avirostris for intermediate food sizes between 15 and 70 μm, and D. denticulatum for small sizes from 2.5 to 15 μm. Penilia avirostris and D. denticulatum acted as passive filter-feeders. Acartia clausi gave some evidence for a supplementary raptorial feeding mode. Effective food concentration (EFC) decreased linearly with increasing nutrient enrichment for D. denticulatum and followed domed curves for A. clausi and for P. avirostris with maximum values at intermediate and high enrichment levels, respectively. Clearance rates of crustacean species showed curvilinear responses with narrow modal ranges to increasing food concentration. Clearance rates of D. denticulatum increased abruptly and levelled into a plateau at low food concentrations. Mean clearance rates were 13.9, 25.5 and 64.1 mL ind.−1 day−1, respectively. No clearance could be detected for A. clausi at food concentrations 〈0.1 mm3 L−1 and for P. avirostris at food concentrations ≤0.02 mm3 L−1. Ingestion rates indicate a rectilinear functional response for A. clausi and for P. avirostris and showed a sigmoidal curve for D. denticulatum. Mean ingestion rates were 1.3, 2.8 and 7.7 μg C μg Cind.−1 day−1, respectively. Conversion of ingested carbon to tissue was 30–80% for the investigated crustaceans and 20–50% for doliolids. Food niche calculations suggest that food niche separation may explain the coexistence of the three species in summer in Blanes Bay.

Description: The δ15N of marine mesozooplankton species was measured on four occasions. Significant differences were found between copepods and meroplanktonic larvae, yet not between holoplanktonic species. On average, mesozooplankton was enriched by 3.4 ± 0.9‰ relative to selected seston size fractions. Despite suggesting small differences (∼0.5 to 1‰) in the δ15N of different phytoplankton taxa on one occasion, the size fractionation procedure generally proved inadequate in separating major taxonomic groups composing seston. This circumstance, and phase-shifts in the transmission of rapid changes (〉2‰) in seston δ15N to mesozooplankton complicate the calculation of mesozooplankton trophic levels.