Juying Li

Stereoisomeric Isolation and Stereoselective Fate of Insecticide Paichongding in Flooded Paddy Soils

Chiral insecticide paichongding (IPP) is one of the prospective substitutes for imidacloprid used in China due to its higher activity against imidacloprid-resistant insects. However, little is known about the fate of IPP in soils, including especially the different behaviors among its stereoisomers. In this study, four stereoisomers of IPP were separated and applied in flooded soils. Kinetics of mineralization, extractable residues, and bound residues showed diastereoselectivity in IPP degradation, with enantiomers (5S,7R)-IPP (IPP-SR) and (5R,7S)-IPP (IPP-RS) being more readily mineralized and preferentially bound to soils than enantiomers (5R,7R)-IPP (IPP-RR) and (5S,7S)-IPP (IPP-SS). The overall mineralization was rather limited and did not exceed 4% of the spiked rate. Concurrent to the decreases of extractable residues, the fraction of bound residues increased with time and reached about 34% of the applied radioactivity for (14)C-IPP-SR and (14)C-IPP-RS as compared to about 23% for (14)C-IPP-RR or (14)C-IPP-SS. Soil properties such as organic matter content and pH likely contributed to the variability. Relatively rapid formation of bound residue suggests that IPP may be quickly detoxified in flooded paddy soil, decreasing the potential for off-site transport such as leaching or runoff, especially for enantiomers IPP-SR and IPP-RS.

Stereoselective uptake and distribution of the chiral neonicotinoid insecticide, Paichongding, in Chinese pak choi (Brassica campestris ssp. chinenesis)

Neonicotinoid chiral insecticidal Paichongding is a promising substitute for the widely used imidacloprid. Four stereoisomers of Paichongding, 5R,7R, 5S,7S, 5S,7R and 5R,7S, were employed in both foliage and roots of Chinese pak choi to investigate their stereoselective uptake and distribution in pak choi. Results showed that after foliar application, no stereoselective absorption into pak-choi plants was observed among the enantiomers. Total absorptions were 35.40% of the applied amount for 5R,7R, 36.66% for 5S,7S, 36.80% for 5S,7R and 38.20% for 5R,7S at 96 HAT. The translocation of the four absorbed stereoisomers within pak choi occurred both acropetally and basipetally and the transport of (14)C from enantiomers 5R,7R and 5S,7S were significantly higher than for 5R,7S and 5S,7R. Significant stereoselective translocation inside plants was observed between Paichongding epimers. Total root uptake reached 16.49-19.85% for 5R,7R and 5S,7S, and 24.57-28.82% for 5S,7R and 5R,7S at 144 HAT. Both enantioselective and diastereoselective root uptake into pak-choi occurred between the four stereoisomers. The 5R,7S and 5S,7R enantiomers were more readily uptaken by the roots than 5R,7R and 5S,7S and accumulated in the edible leaves. These results will help to develop an understanding of Paichongding using only the target-active enantiomer of pesticides.

Soil Microbial Effects on the Stereoselective Mineralization, Extractable Residue, Bound Residue, and Metabolism of a Novel Chiral Cis Neonicotinoid, Paichongding

Fate characteristics of the four stereoisomers of paichongding [IPP, 1-((6-chloropyridin-3-yl)methyl)-7-methyl-8-nitro-5-propoxy-1,2,3,5,6,7-hexahydroimidazo[1,2-a]pyridine] in aerobic sterilized and nonsterilized fluvio-marine yellow loamy soil were investigated using a (14)C tracer technique combined with HPLC and LC-MS/MS. Results showed that the mineralization and bound residue (nonsterile/sterilized soil, % of applied amount) of four stereoisomers of IPP were 1.76-6.10/0.33-0.82 and 12.01-31.20/6.58-20.81 at 100 days after treatment. Seven and five incomplete intermediates of IPP were detected in nonsterilized and sterilized soil, respectively, and a possible degradation pathway was proposed. Degradation mainly occurred on the tetrahydropyridine ring, including oxidation and elimination of the methyl, propyl, and nitro groups. All of these results suggest that soil microbial activity greatly contributes to the epimeride-selective mineralization, formation of bound residue, and degradation of IPP in loamy soil. The identified transformation intermediates could be used for further study on their toxicity to target and nontarget species.

Enantioselective Uptake and Translocation of a Novel Chiral Neonicotinoid Insecticide Cycloxaprid in Youdonger (Brassica campestris subsp. Chinensis)

For a novel potential commercial chiral pesticide, an independent study on the fate characteristics and residues of each stereoisomer is essential if the application rates for the pesticide and human exposure are to be reduced. The absorption and translocation behavior of a chiral insecticide, cycloxaprid, in plants treated by root immersion and blade smearing was studied using (14)C-labeling tracer techniques. With the root treatment, total absorption of (1R;8S)-cycloxaprid (RS) (12.39%) was much greater than that of (1S;8R)-cycloxaprid (SR) (3.31%) at 192 h after treatment (HAT). The mass concentrations (RS/SR) of cycloxaprid in the roots, cotyledons, leaf 1, leaf 2, and leaf 3 were 37.0/16.8, 8.3/2.8, 11.7/6.5, 5.1/4.8, and 8.0/4.7 mg kg(-1) (fresh weight), respectively, at 192 HAT at an initial concentration 1.6 mg kg(-1). With the foliar application treatment, no significant difference was observed between the total absorption of RS (3.11%) and SR (4.03%) at the end of the treatment. Both acropetal and basipetal transport of absorbed (14)C occurred and more than 71.83% of absorbed RS and 82.42% of SR remained in the treated leaf. Stereoselective absorption was observed during root uptake but not during foliar absorption.

Uptake and translocation of 14C-Carbamazepine in soil-plant systems

Carbamazepine (CBZ) is an antiepileptic drug that is frequently detected in wastewater treatment plants, soil and plants after irrigation with treated wastewater or application of biosolids. However, little information is available on the fate and uptake of CBZ in edible vegetables. In this study, radioautographic visualization of the 14C distribution revealed that 14C-CBZ can be taken up by all three ready-to-eat vegetables. Furthermore, a mass-balance study was conducted to evaluate the dynamic processes of the uptake and translocation of CBZ by 14C labeling. 14C-CBZ was gradually taken up with the growth of vegetables, with maximum uptake ratios of 2.19 ± 0.15, 2.86 ± 0.24 and 0.25 ± 0.05% of applied 14C in celery, carrot and pak choi, respectively. The bioconcentration factors (BCFs) based on 14C measurements ranged from 7.6 to 26.1 for celery, 3.6-12.9 for carrot, and 4.4-44 for pak choi. 14C-CBZ was easily translocated from the roots to the leaves and/or stems. The amendment of biosolids had a significant inhibitory effect on the uptake and translocation of 14C-CBZ from soil.