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Phosphorus (P) over-loading is often a central topic due to its linkage to harmful algal blooms (HABs) and its importance in wastewater treatment that has fueled immediate remediation attempts to reduce P loading from point (e.g., wastewater) and nonpoint sources (e.g., fertilizers). Conventional remediation techniques (e.g., filtration) are often expensive, ineffective, and difficult to implement at large scales. The flue gas desulfurization (FGD) gypsum produced as an energy plant waste byproduct has recently been advocated as a physiochemical remediation strategy for P through sorptive removal. However, limited research is available on the practical applications of FGD gypsum for P removal from water. Herein, batch sorption experiments were performed to
investigate the sorptive removal efficiency of P by FGD gypsum under environmentally relevant P concentrations (0.01–0.25 mM). In parallel, fixed-bed column experiments packed with FGD gypsum were performed using elevated P concentrations (0.1–1.0 mM) to understand the scalability of FGD gypsum for large-scale practical applications. During batch experiments, P sorption equilibrium was reached within 24 h that includes an initially fast step (via boundary layer diffusion), followed by a slow rate-determining step (via intraparticle diffusion). P sorption kinetics followed the pseudo second-order kinetics, indicating chemisorption. P sorption at equilibrium can be simulated by both the Freundlich and Langmuir sorption isotherms. The Langmuir sorption isotherm
yielded a maximum sorption capacity (Qmax) of 36.1 mM kg 1. The fixed-bed column experimental results showed that sorption rate depends on the applied flow rate, irrespective of the tested P concentrations. Our findings can be extrapolated to evaluate the feasibility and scalability of FGD gypsum in removing P to counteract P runoff and mitigate HABs and P-loaded wastewater.

1. Chemically reduced nitrogen forms are increasing in aquatic systems and beginning to reach concentrations not previously measured. Despite this, little research has examined the potential of reduced nitrogen forms to encourage excess nitrogen storage and promote algal bloom longevity compared to oxidised forms.
2. A 2-week field, pulse-application experiment was carried out using 1,100-L plastic limnocorrals to examine cyanobacterial community response to three nitrogen forms, including nitrate, ammonium, and urea (added as 600 µg N/L). Cell pigments and counts were used to calculate cell-specific pigment concentrations, and cell-associated microcystin concentrations were also measured to examine toxin response to a shift in nitrogen source.
3. Results showed that, upon nitrogen introduction, extracellular nitrogen quickly decreased in accordance with an increase in cellular phycocyanin 72 hr after fertilisation. Ammonium and urea treatments had more phycocyanin/cell than nitrate or control treatments at 72 hr. After 72 hr, phycocyanin content quickly decreased, consistent with the use of nitrogen from phycobiliproteins. Despite the decrease in light-harvesting pigments, the total number of cyanobacterial cells increased in the ammonium and urea treatments after 2 weeks. Cyanobacterial particulate toxin (microcystin) quotas were not affected by nitrogen additions.
4. Results show that reduced nitrogen forms encourage greater nitrogen storage as pigments and increase bloom longevity compared to oxidised forms.
5. Findings support previous studies that suggest reduced nitrogen forms encourage greater cell density and algal bloom persistence. Results further point to excess nitrogen storage as another mechanism that allows cyanobacteria to dominate freshwater systems despite variable environmental conditions.