No abstract

The accumulation of radioactively labelled strontium and zinc by living and killed tips of the brown alga Ascophyllum nodosum (L.) Le Jol. was studied and compared with the uptake in some model substances. The accumulation of strontium was reversible, and similar in living and killed plants. Equilibrium was established within a couple of days. Strontium accumulation seemed to be an ionexchange process involving the negatively charged intercellular polysaccharides, probably mainly alginate. Only a small fraction of the zinc uptake in living algae seemed to be due to a similar ion exchange with the intercellular polysaccharides. The characteristic features of the zinc uptake was a constant, slow, irreversible accumulation persisting for very long periods of time. In dead algae the uptake was rapid and reversible, indicating that the algae contained zinc‐binding substances which were not directly accessible to the zinc ions in the surrounding seawater before killing. It is proposed that these substances in the living plant are contained in membrane‐surrounded structures, probably vacuoles. These membranes, effectively regulating the zinc uptake in the living cells, are destroyed by killing, making the zinc binding substances directly accessible. The transfer of zinc from the reversible intercellular sites to the irreversible cellular sites continued undisturbed during low‐tide periods. The intercellular charged polysaccharides thus function as ion buffers, allowing ion uptake into the cell at a constant rate, independent of the tidal movements.

The present cage culture turbidostat consists of a growth chamber and a control unit. The microorganisms (photoautotrophic algae) are kept in the growth chamber by porous membranes (pore size 1 to 3 μm) which retain the algae but allow efficient exchange of the growth medium. Flow rate and composition of the medium can therefore be varied independently of algal population density. A reciprocating pumping mode of the medium is introduced to obtain more gentle clearance of membranes than that provided by rotation or stirring in other membrane fermentors. Pulsed light and a light-emitting diode/light-sensitive transistor couple are used to monitor the turbidity of the culture, independent of external light needed for growth. The control unit keeps the turbidity constant by frequent activation of the dilution pump. Theoretical analysis of growth in the turbidostat shows that integrated activation time of the dilution pump is proportional to the growth rate of the organism. Theoretical analysis was also used to determine minimum flow-rate and nutrient concentration of medium to cover the requirement of the algae. Experiments with three different marine diatoms were carried out, and they demonstrated that the growth rate could be determined every hour and that the cultures could be kept at constant turbidity over 10 to 14 days at least.