Hydrogen peroxide can be a plausible biomarker in cyanobacterial bloom treatment.

The effect of combined stresses, photoinhibition, and nutrient depletion on the oxidative stress of cyanobacteria was measured in laboratory experiments to develop the biomass prediction model. Phormidium ambiguum was exposed to various photosynthetically active radiation (PAR) intensities and phosphorous (P) concentrations with fixed nitrogen concentrations. The samples were subjected to stress assays by detecting the hydrogen peroxide (H2O2) concentration and antioxidant activities of catalase (CAT) and superoxide dismutase (SOD). H2O2 concentrations decreased to 30 µmol m-2 s-1 of PAR, then increased with higher PAR intensities. Regarding P concentrations, H2O2 concentrations (nmol L-1) generally decreased with increasing P concentrations. SOD and CAT activities were proportionate to the H2O2 protein-1. No H2O2 concentrations detected outside cells indicated the biological production of H2O2, and the accumulated H2O2 concentration inside cells was parameterized with H2O2 concentration protein-1. With over 30 µmol m-2 s-1 of PAR, H2O2 concentration protein-1 had a similar increasing trend with PAR intensity, independently of P concentration. Meanwhile, with increasing P concentration, H2O2 protein-1 decreased in a similar pattern regardless of PAR intensity. Protein content decreased with gradually increasing H2O2 up to 4 nmol H2O2 mg-1 protein, which provides a threshold to restrict the growth of cyanobacteria. With these results, an empirical formula-protein (mg L-1) = - 192*Log((H2O2/protein)/4.1), where H2O2/protein (nmol mg-1) = - 0.312*PAR2/(502 + PAR2)*((25/PAR)4 + 1)*Log(P/133,100), as a function of total phosphorus concentration, P (µg L-1)-was developed to obtain the cyanobacteria biomass.

Effects of elevated pressure on Pseudanabaena galeata Böcher in varying light and dark environments.

To understand the effect of the hydrostatic pressure on Pseudanabaena galeata Böcher cells in both stratified and frequently mixed lakes, separate laboratory-scale models were developed. The pressure conditions in the stratified and mixed lakes were simulated in those models, and the variations of the cell and chlorophyll-a (Chl-a) concentration were analyzed. It was observed that an increase in pressure and darkness significantly reduced the cell concentration and pigmentation in P. galeata (p < 0.01, n = 3). After 10 days, the cell concentrations of P. galeata that were grown under conditions of a water depth of 30 m were reduced by 7.0%, per day, while the cell concentration rate after 10 days in atmospheric conditions was increased by 2.53% per day. During the experiment, cells were subjected to the prolonged darkness under 0.3 MPa pressure for 10 days and then exposed to the white light under atmospheric pressure for 5 days. Even after running this cycle for 60 days, 19.5% of the initial cells could survive. This rate exceeded the cell concentration-increasing rate in the control. These findings indicate that P. galeata has an adequate tolerance to pressure and fluctuating light irradiance and that the cells are able to propagate after escaping from those stress conditions.

Buoyancy Limitation of Filamentous Cyanobacteria under Prolonged Pressure due to the Gas Vesicles Collapse.

Freshwater cyanobacterium Pseudanabaena galeata were cultured in chambers under artificially generated pressures, which correspond to the hydrostatic pressures at deep water. Variations occurred in gas vesicles volume, and buoyancy state of cells under those conditions were analyzed at different time intervals (5 min, 1 day, and 5 days). Variations in gas vesicles morphology of cells were observed by transmission electron microscopy images. Settling velocity (Vs) of cells which governs the buoyancy was observed with the aid of a modified optical microscope. Moreover, effects of the prolonged pressure on cell ballast composition (protein and polysaccharides) were examined. Elevated pressure conditions reduced the cell ballast and caused a complete disappearance of gas vesicles in Pseudanabaena galeata cells. Hence cyanobacteria cells were not able to float within the study period. Observations and findings of the study indicate the potential application of hydrostatic pressure, which naturally occurred in hypolimnion of lakes, to inhibit the re-suspension of cyanobacteria cells.