Preparation of Emamectin Benzoate·Hexaflumuron Granules Based on Response Surface Methodology.

In order to obtain particles with an optimal loading rate and encapsulation efficiency and to explore the effects of sodium alginate, carboxymethyl chitosan, and bentonite on the particle loading rate and encapsulation rate, the preparation parameters of particles were optimized by the response surface method. A series of particles with constantly changing components were prepared, and the particle loading rate and encapsulation rate were determined. The release experiment of granules in different mass release media was implemented, and the optimal loading rate and encapsulation efficiency of particles were used to control the fall armyworm (FAW). The results showed that when the amount of sodium alginate was 1.83%, that of carboxymethyl chitosan was 0.41% and that of bentonite was 0.37%. The maximum theoretical value based on the response surface simulation was 92.63%, and the actual value at this ratio was 91.61%, which was 98.90% of the theoretical value. The release assay indicated that the mechanism of particle release in 2, 4, and 6 mL of the release medium was non-Fickian diffusion, and the controlled mechanism in 25 mL of the medium was Fickian diffusion. The beads were spread directly into maize leaf whorls in field production; at 14 days after application, the efficacy reached 91.28-98.82%. The combination of emamectin benzoate and hexaflumuron granules has a good control effect on the FAW.

Enantioselective bioaccumulation and toxicity of rac-sulfoxaflor in zebrafish (Danio rerio).

Sulfoxaflor is a fourth-generation neonicotinoid insecticide mainly used to control sap-feeding pests. In this study, four stereoisomers of sulfoxaflor were separated using HPLC, and the absolute configurations of three stereoisomers were identified via single-crystal X-ray diffraction. First, the stability and isomerization of the four enantiomers and rac-sulfoxaflor in water and seven organic solvents were investigated. All enantiomers were extremely unstable in water with isomerization rates above 20%. The racemate did not isomerize in any of the solutions and was stable in water (degradation rate less than 7%). Therefore, we studied the acute toxicity, enantioselective behavior, and enzymatic activities of rac-sulfoxaflor in zebrafish. The bioaccumulation experiment demonstrated that the bioconcentration of sulfoxaflor in zebrafish was enantioselective, and the four enantiomers accumulated in zebrafish in the order (+)-2S,3S-sulfoxaflor > (-)-2R,3R-sulfoxaflor > (+)-2R,3S-sulfoxaflor > (-)-2S,3R-sulfoxaflor. The effect of rac-sulfoxaflor on the enzymatic activities of zebrafish showed that superoxide dismutase and glutathione-S-transferase activities and malondialdehyde content were significantly enhanced as compared to those in control, whereas acetylcholinesterase was significantly reduced in the sulfoxaflor exposure treatment (p < 0.05), indicating that sulfoxaflor caused oxidative lesions and induced enzymatic activity in zebrafish. This study provides important information on the enantioselective behavior and toxic effects of sulfoxaflor, which can help assess the potential ecological risk of chiral pesticides to aquatic organisms.

Dissipation and sorption-desorption of benzisothiazolinone in agricultural soils and identification of its metabolites.

Benzisothiazolinone has been widely used to control bacterial and fungal diseases in various agricultural crops by destroying the nuclear structure and interfering with the metabolism of microbial cells. In this study, the dissipation, transformation and sorption-desorption of benzisothiazolinone (BIT) in five soils were investigated to evaluate its environmental fate. Results showed that the degradation of BIT in all the tested soils fitted the first order kinetics and increased with soil organic matter (OM) content. Degradation differences between unsterilized natural and sterilized soils (t 1/2 = 0.09-26.66 and 6.80-86.64 d) suggested that BIT degradation is primarily driven by biological processes and assisted by abiotic degradation. Additionally, BIT dissipated fastest in flooded soils (t 1/2 = 0.20-4.53 d), indicating that anaerobic microorganisms are more likely to degrade BIT compared to aerobic microbes. Also, during the soil degradation process, two metabolites were monitored and identified for the first time. BIT sorption was a spontaneous physical process with no desorption hysteresis effect, which fit the Freundlich model. BIT causes relatively strong sorption (log K OC = 3.76-4.19) and low persistence in soils, thus exhibiting a low potential risk for groundwater contamination.

Oxidative Stress and Enantioselective Degradation of Dufulin on Tubifex.

Dufulin is a new type of chiral antiplant virus agent independently developed in China. The present study was conducted to determine the effects of different concentrations of rac-dufulin and dufulin enantiomers (1, 5, and 10 mg/L) on oxidative stress in Tubifex after exposure for 3, 7, and 14 d. Results showed that rac-dufulin and individual enantiomers had no significant effects on total protein content and glutathione reductase activities. Increased superoxide dismutase demonstrated the generation of superoxide anion radical. The increase in glutathione S-transferase may be due to detoxification mechanisms. The different changes in catalase activities could be due to oxidative stress. The increase in malondialdehyde may be due to the accumulation and toxicity of contaminations. The degradation behavior of dufulin enantiomers was studied through spiked-water and spiked-soil tests. The degradation rate of S-(+)-dufulin was faster than that of R-(-)-dufulin. The present study demonstrated the occurrence of enantioselectivity in the degradation and oxidative stress of dufulin to Tubifex. In spiked soil, the concentrations of dufulin enantiomers in underlying soil were significantly higher than those in overlying water; but after 5 d of degradation, the bioturbation of Tubifex could facilitate part of dufulin diffusing from the underlying soil into the overlying water and altered the partitioning of dufulin. The present study provided a basis for conducting environmental safety risk assessments and rationally using dufulin as a chiral pesticide. Environ Toxicol Chem 2020;39:2136-2146. © 2020 SETAC.