4.6 Article

The influence of experimentally generated turbulence on the Mash01 unicellular Microcystis aeruginosa strain

Journal

HYDROBIOLOGIA
Volume 517, Issue 1-3, Pages 107-120

Publisher

SPRINGER
DOI: 10.1023/B:HYDR.0000027341.08433.32

Keywords

small-scale turbulence; Microcystis; flow cytometry; fluorescent dyes

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Phytoplankton experience a continuously changing fluid environment and the response to this is reflected at individual and community levels. The large-scale motions of winds, waves and artificial circulations are coupled by turbulence to the viscous small-scale environment of the phytoplankton cell. To investigate the significance of turbulence in the ecology of Microcystis aeruginosa, cultures were exposed to turbulent conditions using a vertically oscillating grid for a period of 7 days under controlled laboratory conditions. M. aeruginosa was exposed to a range of turbulent intensities, by adjusting the frequency of oscillation from 1 to 4 Hz. To improve the resolution of scale between turbulence phenomena and phytoplankton, flow cytometry and fluorescent probes were used to assess the response of M. aeruginosa. Metabolic activity and cell viability were monitored daily in both the turbulent cultures and quiescent control cultures using the FDA and Sytox green fluorescent probes, respectively. Initially, low turbulence levels generated by the grid at frequencies of 1 and 2 Hz stimulated metabolic activity, and did not affect cell viability compared to the control quiescent cultures. However, higher levels of turbulence generated by the grid at frequencies of 3 and 4 Hz were deleterious to metabolic activity and viability. Metabolic activity significantly decreased and over 85% of cells were nonviable after 96 h at a grid oscillation of 4 Hz. It was concluded that due to the long lag time (> 96 h) and high intensities needed to exert a deleterious effect, small-scale turbulence is unlikely to be a significant factor controlling M. aeruginosa compared to large scale motion which lead to changes in light and nutrient conditions.

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