Turbidostat cultures of Dunaliella salina (Chlorophyceae) and Thalassiosira weissflogii (Bacillariophyceae) were grown at fluctuating concentrations of nitrate, phosphate and silicate. In-line measurements of PAM fluorescence were used to monitor the effects of fluctuating nutrient supply on the photochemical efficiency of photosystem II reaction centres of light-adapted cells (ΔF/F'm). Besides the maximal photochemical efficiency of photosystem II reaction centres of dark-adapted cells (Fv/Fm), chlorophyll a, particulate organic carbon, nitrogen and phosphorus, and the cell number were measured frequently during the experiments. Following nutrient-replete growth, the cells were supplied with medium from which either nitrate, phosphate or silicate was omitted. When significant effects of nutrient starvation were indicated by the fluorescence parameters, a pulse of the deficient nutrient was added to the cultures. Our experimental set-up for in-line fluorescence measurements provided sensitive and reproducible detection of the various fluorescence signals, revealing strong influences of nutrient supply on the photochemical efficiency of photosystem II. In general the fluorescence values changed substantially within 1–30 min after re-addition of the deficient nutrient. Addition of phosphate and silicate induced an immediate characteristic decrease in fluorescence, whereas nitrate addition was characterized by a strong, delayed increase in fluorescence. Complete recovery to pre-starvation fluorescence values took about 48 h in all experiments. The physiological background of nutrient uptake is used to explain the observed tight couplings between fluorescence responses and nutrient re-addition. Our study clearly demonstrates that in-line fluorescence measurements provide a new tool for the investigation of phytoplankton reactions to fluctuating nutrients and offer the possibility to detect nutrient starvation in the field.

The dependence of the cellular (biogenic) and frustule-associated (mineralized) silica content of the diatoms Navicula salinarum and Thalassiosira weissflogii on salinity and aluminium conditions was studied in order to make it possible to manipulate silicification in vitro and maximize it to levels required for physico-chemical frustule characterization by physisorption, X-ray scattering analysis and NMR, which is our ultimate objective. Enrichments with AlCl3 increased growth and the final cell density of the pennate N. salinarum, but not of the centric species T. weissflogii. Aluminium additions did not, however, result in a significant increase in the biogenic or mineralized silica content per cell and could not be detected in the silica matrix of the frustule. In contrast, lowering the salinity from 28 practical salinity units (PSU) to 20 and 15 resulted in a significant increase in the biogenic silica content per cell of both species, which is in line with an increase in density of the chemically derived silica under low salt conditions. The silica content per cell was variable during culture growth; increase in cell densities (during exponential growth) was accompanied by a decrease in contents of biogenic silica per cell. Electron microscopy and energy dispersive X-ray analysis (EDXA) support the chemical analyses and also suggest higher biogenic silica contents at lower salinities. The results indicate that besides silicate concentration and pH, the concentration of salts is an important inorganic factor that affects the silica polymerization inside the silica deposition vesicle of diatoms.

We report the cloning and characterization of a 1881 bp Thalassiosira weissflogii (Bacillariophyceae, Centrales) plastid genomic fragment containing the ferredoxin gene (petF) and several other genes. The organization of this fragment is exactly the same as its equivalent region from the plastid genome of another centric diatom, Odontella sinensis, and the sequences share high homology in both coding and non-coding regions. Traces of a probable vestigial protein-coding gene and of a partial trn gene are found just after the trnR gene in both diatoms as well as in the plastid genome of the red alga Porphyra purpurea, illustrating the close relationship between red algal and heterokont algal plastid genomes and arguing in favour of the origin of the latter by secondary endosymbiosis. In accordance with phylogenetic analyses of most plastid genes, phylogenetic trees inferred from 69 ferredoxin sequences show that both the green and the red algal plastid genes arose from cyanobacterial genes; our results furthermore suggest that each of these plastid lineages is related to different extant cyanobacterial genes, implying either that different endosymbiotic events were responsible for the origin of green and red plastids or that each lineage kept only one (and a different one) of several paralogous cyanobacterial genes present in the ancestral cyanobacterial genome.