Microcystis blooms have become a ubiquitous phenomenon in freshwater ecosystems, and the size of Microcystis colonies varies widely throughout the year. In the present study, hydrogen peroxide (H₂O₂) was applied to test the effect of this algaecide on Microcystis colonies of different sizes and to evaluate the colonies' antioxidant strategy. The results showed that Microcystis populations collapsed under treatment with 5 mg/L H₂O₂ at colony sizes smaller than 25 μm. A dosage of 20 mg/L H₂O₂ was necessary to efficiently control Microcystis colonies larger than 25 μm. The enzymatic and non-enzymatic antioxidant systems of different colonies exhibited various strategies to mitigate oxidative stress. In small colonies, superoxide dismutase (SOD) activity was readily stimulated and operated with catalase (CAT) activity to eliminate reactive oxygen species (ROS). In colonies larger than 25 μm, the antioxidant enzyme CAT and antioxidant substance glutathione (GSH) played major roles in mitigating oxidative stress at H₂O₂ concentrations below 20 mg/L. In addition, application of the algaecide led to the release of intracellular-microcystins (MCs), and oxidatively-driven MCs reached high concentrations when colony size was larger than 100 μm. Algaecide control measures should be implemented before the formation of large colonies to limit the algaecide dosage and MC release.

Bisphenol A (BPA) is an important industrial chemical; bisphenol S (BPS) is a substitute for BPA. Both are frequently detected in rivers, sewage, and surface water, and have a great impact on the water environment. The effects of BPA and BPS on cell growth, chlorophyll a content, and oxidative stress of Chlorella pyrenoidosa (C. pyrenoidosa) were studied. When BPA and BPS acted alone or in combination, compared with the blank control group, the growth of C. pyrenoidosa in the experimental group showed a pattern of “low promotion and high inhibition”, and the inhibition rate reached the maximum on the 6th day. Under the combined action, the reactive oxygen species (ROS) level of C. pyrenoidosa first increased, and then decreased. In addition, the activity of superoxide dismutase (SOD) and peroxidase (POD) increased with the increase in combined concentration. In the 0.5 P treatment group, SOD and POD activity reached peak values of 29.59 U/mg∙prot and 1.35 U/mg∙prot, respectively. The combined toxicity of BPA and BPS to C. pyrenoidosa was evaluated as a synergistic effect by using toxicity unit and additive index methods. This study evaluated the effects of BPA and BPS on algae in the aquatic environment, providing some data support for their potential ecological risks.

Microcystis blooms and microcystins caused by eutrophication are harmful to the environment. At present, algicide based on allelochemicals is widely used in algae control. Environment-friendly sustained-release salicylate chitosan microspheres (SA-CS) were prepared by acylation of chitosan and glutaraldehyde. SA-CS was characterized by scanning electron microscopy, Fourier transform infrared spectral analysis, and laser particle sizer. The inhibitory effects of SA-CS on Microcystis aeruginosa at different stages, and the environmental impact of the inorganic index, were studied. The results showed that the mean size of SA-CS was 53.3 μm, the encapsulation rate was 40.66%, and SA-CS had a good sustained-release effect (stable release within 25 days). On the seventh day, a 90% inhibition rate in the lag phase required 105 mg/L of SA-CS, whereas a 90% inhibition rate in the log phase required 675 mg/L of SA-CS. The sensitivity of Microcystis aeruginosa at the lag phase to salicylic acid was about 1.4 times that of the log phase, thus, it is recommended to control the algae in the lag phase. The long-term inhibition effect of SA-CS on algae was detected after adding sufficient SA-CS. In terms of salicylic acid, pH, and dissolved oxygen, no lousy effect was observed for the addition of SA-CS. SA-CS could effectively reduce the concentration of microcystin-LR by 50%. SA-CS is an environment-friendly sustained-release microsphere with good algal inhibition performance for Microcystis aeruginosa.