Lanthanum-modified bentonite (LMB) has remarkable efficacy on eutrophication control, but the reduced bioavailable phosphorus and formed anaerobic horizon from LMB may be harmful to submerged macrophytes. We conducted this study to explore the influence of LMB on Hydrilla verticillata and Vallisneria natans in mixed-species plantings. The concentrations of TP, TDP, SRP, and TDN in the LMB treatments were lower than the Control, but the Chl a concentration in the HLMB treatment (850 g m⁻²) was higher than the Control by 63%. There were no differences of V. natans growth among the treatments. For H. verticillata, its biomass, RGR, height, branch number, root number, and length in the LLMB treatment (425 g m⁻²) were lower than the Control by 48%, 22%, 13%, 34%, 33%, and 8%, respectively. In addition, the biomass of H. verticillata was 62%, the RGR was 32%, the height was 19%, the branch number was 52%, the root length was 40%, and the root number was 54% lower in the HLMB treatment than those in the Control. In summary, LMB had negative effects on submerged macrophytes with underdeveloped roots. Submerged macrophytes with more developed roots are preferred when using combined biological–chemical methods for water restoration.

With the increasing use and release of plastic products, microplastics have rapidly accumulated in ecological environments. When microplastics enter the food chain, they cause serious harm to organisms and humans. Microplastics pollution has become a growing concern worldwide; however, there is still no standardized method for rapidly and accurately detecting microplastics. In this work, we used fluorescence lifetime imaging technology to detect four kinds of Nile red-stained and unstained microplastics, and the unique phasor fingerprints of different microplastics were obtained by phasor analysis. Tracing the corresponding pixels of the “fingerprint” in the fluorescence lifetime image allowed for the quick and intuitive identification of different microplastics and their location distributions in a mixed sample. In our work, compared with staining the four microplastics with a fluorescent dye, using the phasor “fingerprint library” formed by the autofluorescence lifetimes of the microplastics was more easily distinguished than microplastics in the mixed samples. The feasibility of this method was further tested by adding three single substances—SiO₂, chitin and decabromodiphenyl ethane (DBDPE), and surface sediments to simulate interferent in the environment, and the results providing potential applications for the identification and analysis of microplastics in complex environments.