Figure 2
Photographs of aggregates following a 72-hour aggregation period in the roller tanks. Set-up 1 (a, b) included high concentrations of microbeads only, estimated at 24000 and 16000 L–1 (treatments 1 and 2, respectively); set-up 2 (c, d), same high concentrations of microbeads, aggregated with 106 cells L–1 of T. weissflogii (treatments 4 and 5, respectively); set-up 3 (e, f), moderate concentrations of microbeads, estimated at 4000 and 2000 L–1 (treatments 8 and 9, respectively), aggregated with 106 cells L–1 of T. weissflogii; and set-up 4 (g, h), same moderate concentrations of microbeads, aggregated with 106 cells L–1 of T. weissflogii, and 130 mg sediments (treatment 12). Images in panels a–f were taken in aggregation tanks for treatments 1, 2, 4, 5, and 8, 9, respectively (Table 1). Images in panels g and h were taken in the settling columns from treatment 12. A fishing line of 250 μm in diameter (as in panels g and h) was used to calibrate image size. DOI: https://doi.org/10.1525/elementa.317.f2

Photographs of aggregates following a 72-hour aggregation period in the roller tanks. Set-up 1 (a, b) included high concentrations of microbeads only, estimated at 24000 and 16000 L–1 (treatments 1 and 2, respectively); set-up 2 (c, d), same high concentrations of microbeads, aggregated with 106 cells L–1 of T. weissflogii (treatments 4 and 5, respectively); set-up 3 (e, f), moderate concentrations of microbeads, estimated at 4000 and 2000 L–1 (treatments 8 and 9, respectively), aggregated with 106 cells L–1 of T. weissflogii; and set-up 4 (g, h), same moderate concentrations of microbeads, aggregated with 106 cells L–1 of T. weissflogii, and 130 mg sediments (treatment 12). Images in panels a–f were taken in aggregation tanks for treatments 1, 2, 4, 5, and 8, 9, respectively (Table 1). Images in panels g and h were taken in the settling columns from treatment 12. A fishing line of 250 μm in diameter (as in panels g and h) was used to calibrate image size. DOI: https://doi.org/10.1525/elementa.317.f2

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