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BACKGROUND: Flusulfinam, a novel chiral herbicide, effectively controls Echinochloa crusgalli and Digitaria sanguinalis in paddy fields, indicating significant potential for practical agricultural applications. However, limited information is available on flusulfinam from a chiral perspective. A comprehensive evaluation of the enantiomeric levels of flusulfinam was performed. RESULTS: Two enantiomers, R-(+)- and S-(-)-flusulfinam, were separately eluted using a Chiralcel OX-RH column. The bioactivity of R-flusulfinam against the two was 1.4-3.1 fold that of Rac-flusulfinam against two weed species. R-flusulfinam toxicity to Danio rerio larvae and Selenastrum capricornutumwere was 0.8- and 3.0-fold higher than Rac-flusulfinam, respectively. Degradation experiments were conducted using soil samples from four Chinese provinces. The findings indicated that S-flusulfinam (half-life T1/2 = 40.8 days) exhibits preferential degradation than R-flusulfinam (T1/2 = 46.2-57.8 days) in the soils of three provinces. Under anaerobic conditions, soil from Anhui exhibited preferential degradation of R-flusulfinam (T1/2 = 46.2 days) over S-flusulfinam (T1/2 = 63 days). Furthermore, two hydrolysis products of flusulfinam (M299 and M100) are proposed for the first time. CONCLUSION: The enantioselective bioactivity, toxicity and degradation of flusulfinam were investigated. Our findings indicate that R-flusulfinam is an extremely effective and low-toxicity enantiomer for the tested species. The soil degradation test indicated that the degradation of flusulfinam was accelerated by higher organic matter content and lower soil pH. Furthermore, microbial communities may play a crucial role in driving the enantioselective degradation processes. This study lays the groundwork for the systematic evaluation of flusulfinam from an enantiomeric perspective. © 2024 Society of Chemical Industry.
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In this study, the role of E3 ubiquitin ligase GmSNE3 in halosulfuron methyl (HSM) inhibiting soybean nodulation was investigated. GmSNE3 was strongly induced by HSM stress, and the overexpression of GmSNE3 significantly reduced the number of soybean nodules. Further investigation found that GmSNE3 could interact with a nodulation signaling pathway 1 protein (GmNSP1a) and GmSNE3 could mediate the degradation of GmNSP1a. Importantly, GmSNE3-mediated degradation of GmNSP1a could be promoted by HSM stress. Moreover, HSM stress and the overexpression of GmSNE3 resulted in a substantial decrease in the expression of the downstream target genes of GmNSP1a. These results revealed that HSM promotes the ubiquitin-mediated degradation of GmNSP1a by inducing GmSNE3, thereby inhibiting the regulatory effect of GmNSP1a on its downstream target genes and ultimately leading to a reduction in nodulation. Our findings will promote a better understanding of the toxic mechanism of herbicides on the symbiotic nodulation between legumes and rhizobia.
Assuntos
Regulação da Expressão Gênica de Plantas , Glycine max , Herbicidas , Proteínas de Plantas , Nodulação , Compostos de Sulfonilureia , Ubiquitina-Proteína Ligases , Glycine max/genética , Glycine max/metabolismo , Glycine max/química , Ubiquitina-Proteína Ligases/metabolismo , Ubiquitina-Proteína Ligases/genética , Proteínas de Plantas/genética , Proteínas de Plantas/metabolismo , Herbicidas/farmacologia , Nodulação/genética , Nodulação/efeitos dos fármacos , Regulação da Expressão Gênica de Plantas/efeitos dos fármacos , Compostos de Sulfonilureia/farmacologiaRESUMO
Ralstonia solanacearum is a devastating phytopathogen infecting a broad range of economically important crops. Phosphate (Pi) homeostasis and assimilation play a critical role in the environmental adaptation and pathogenicity of many bacteria. However, the Pi assimilation regulatory mechanism of R. solanacearum remains unknown. This study revealed that R. solanacearum pstSCAB-phoU-phoBR operon expression is sensitive to extracellular Pi concentration, with higher expression under Pi-limiting conditions. The PhoB-PhoR fine-tunes the Pi-responsive expression of the Pho regulon genes, demonstrating its pivotal role in Pi assimilation. By contrast, neither PhoB, PhoR, PhoU, nor PstS was found to be essential for virulence on tomato plants. Surprisingly, the PhoB regulon is activated in a Pi-abundant rich medium. Results showed that histidine kinase VsrB, which is known for the exopolysaccharide production regulation, partially mediates PhoB activation in the Pi-abundant rich medium. The 271 histidine of VsrB is vital for this activation. This cross-activation mechanism between the VsrB and PhoB-PhoR systems suggests the carbohydrate-Pi metabolism coordination in R. solanacearum. Overall, this research provides new insights into the complex regulatory interplay between Pi metabolism and growth in R. solanacearum.
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Proteínas de Bactérias , Regulação Bacteriana da Expressão Gênica , Fosfatos , Doenças das Plantas , Ralstonia solanacearum , Solanum lycopersicum , Ralstonia solanacearum/metabolismo , Ralstonia solanacearum/genética , Fosfatos/metabolismo , Proteínas de Bactérias/metabolismo , Proteínas de Bactérias/genética , Solanum lycopersicum/microbiologia , Virulência , Doenças das Plantas/microbiologia , Regulon , Histidina Quinase/metabolismo , Histidina Quinase/genética , Óperon , Meios de Cultura/químicaRESUMO
Fenoxaprop-p-ethyl (FEN) is an aryloxy phenoxy propionate herbicide that has been widely used in paddy fields. Previous studies have indicated that FEN is highly toxic to aquatic organisms, but little is known about the developmental effects of FEN. This study investigated acute and developmental toxicity, malondialdehyde (MDA) levels, superoxide dismutase (SOD) and catalase (CAT) activities, and metabolomic analyses in zebrafish embryos after 96 h of exposure. FEN exhibited high acute toxicity to zebrafish embryos and larvae. Exposure to FEN could reduce heartbeat and hatching rates and increase malformation rates in embryos. Oxidative damage was also caused in embryos. The results of metabolomics analysis showed that 102 differentially abundant metabolites were found in zebrafish embryos in the 0.05 mg/L FEN treatment group, and 60 differentially abundant metabolites were found in the 0.20 mg/L FEN treatment group. These differentially abundant metabolites mainly belonged to 9 metabolic pathways, of which folate pathways and ABC transport protein pathways had the greatest impact. These results suggested that FEN induced high acute and developmental toxicity in zebrafish embryos.
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Oxazóis , Poluentes Químicos da Água , Peixe-Zebra , Animais , Peixe-Zebra/metabolismo , Propionatos/metabolismo , Estresse Oxidativo , Embrião não Mamífero , Poluentes Químicos da Água/metabolismoRESUMO
Thiamethoxam and microplastics are both common pollutants in farmland soil; however, few studies have focused on the interaction between thiamethoxam and microplastics in soil. Here, a batch experiment and soil incubation experiment were performed to explore the mechanism and effects of microplastics on the adsorption and degradation behaviors of thiamethoxam in soil, respectively. First, the batch experimental results indicated that the adsorption process of thiamethoxam on the microplastic/soil mixtures and soil-only systems mainly relies on chemical interactions. All sorption processes had moderate intensities of adsorption, and the sorption process occurred on the heterogeneous surface. In addition, the particle size and dose of microplastics could both affect the adsorption behavior of thiamethoxam onto microplastics/soil systems. The sorption capacity of thiamethoxam in soil decreases as the particle size of microplastics increases, but the sorption capacity increases as the dose of microplastics increases. Second, the results of the soil incubation experiment showed that the half-lives of thiamethoxam ranged from 57.7 d to 86.6 d, from 86.6 d to 173.3 d, and 115 d in the biodegradable microplastic/soil systems, nondegradable microplastic/soil systems, soil-only systems, respectively. These results indicate that biodegradable microplastics promoted the degradation of thiamethoxam, while nondegradable microplastics delayed the degradation process of thiamethoxam in soil. Overall, microplastics could change the degradation behaviors, sorption capacity and adsorption efficiency, and then affect the mobility and persistence of thiamethoxam in the soil environment. These findings contribute to understanding the influence of microplastics on the environmental fate of pesticides in the soil environment.
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Microplásticos , Poluentes do Solo , Tiametoxam , Solo , Plásticos , Adsorção , Poluentes do Solo/análiseRESUMO
Terbuthylazine (TBA) is an emerging environmental contaminant that poses moderate to high risk to non-target organisms. In this study, a newly TBA-degrading strain, Agrobacterium rhizogenes AT13, was isolated. This bacterium degraded 98.7% of TBA (100 mg/L) within 39 h. Based on the six detected metabolites, three novel pathways of strain AT13, including dealkylation, deamination-hydroxylation, and ring-opening reactions, were proposed. The risk assessment demonstrated that most degradation products might be substantially less harmful than TBA. Whole-genome sequencing and RT-qPCR analysis revealed that ttzA, which encodes S-adenosylhomocysteine deaminase (TtzA), is closely related to TBA degradation in AT13. Recombinant TtzA showed 75.3% degradation of 50 mg/L of TBA within 13 h and presented a Km value of 0.299 mmol/L and a Vmax value of 0.041 mmol/L/min. The molecular docking results indicated that the binding energy of TtzA to TBA was -32.9 kcal/mol and TtzA residue ASP161 formed two hydrogen bonds with TBA at distances of 2.23 and 1.80 Å. Moreover, AT13 efficiently degraded TBA in water and soil. Overall, this study provides a foundation for the characterization and mechanism of TBA biodegradation and may enhance our understanding of the TBA biodegradation by microbes.
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Agrobacterium , Bactérias , Simulação de Acoplamento Molecular , Agrobacterium/genética , Biodegradação AmbientalRESUMO
Agrobacterium rhizogenes AT13, a novel bacterial strain that was isolated from contaminated soil, could utilize atrazine as the sole nitrogen, thereby degrading it. Optimization of the degradation reaction using a Box-Behnken design resulted in 99.94% atrazine degradation at pH 8.57, with an inoculum size of 3.10 × 109 CFU/mL and a concentration of 50 mg/L atrazine. Ultra-high performance liquid chromatography-electrospray ionization-high resolution mass spectrometry (UPLC-ESI-HRMS), liquid chromatography tandem mass spectrometry (LC-MS/MS) and high performance liquid chromatography (HPLC) analyses identified and quantified six reported metabolites and a novel metabolite (2-hydroxypropazine) from atrazine degradation by AT13. On the basis of these metabolites, we propose an atrazine degradation pathway that includes dichlorination, hydroxylation, deamination, dealkylation and methylation reactions. The toxicity of the degradation products was evaluated by Toxicity Estimation Software Tool (T.E.S.T). Bioaugmentation of atrazine-polluted soils/water with strain AT13 significantly improved the atrazine removal rate. Thus, AT13 has potential applications in bioremediation.
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Atrazina , Herbicidas , Poluentes do Solo , Atrazina/química , Herbicidas/química , Biodegradação Ambiental , Cromatografia Líquida , Espectrometria de Massas em Tandem , Microbiologia do Solo , Poluentes do Solo/metabolismoRESUMO
Halosulfuron-methyl (HSM) is a new and highly effective sulfonylurea herbicide widely used in weed control, but its residue in the environment poses a potential risk to soybean. Soybean-rhizobium symbiotic nitrogen fixation is crucial for sustainable agricultural development and ecological environment health. However, the impact of HSM on the symbiosis between soybean and rhizobium is unclear. In this study, the effects of HSM on the soybean-rhizobium symbiotic process and nitrogen fixation were investigated by means of transcriptomic and physiological analyses. Treatment with a concentration of HSM less than 0.5 mg L-1 had no effect on rhizobium growth, but significantly reduced nodules number, the biomass of soybean nodules, and nitrogenase activity in root nodules (P < 0.05). Transcriptomic analysis showed that differentially expressed genes (DEGs) involved in NH4+ assimilation were significantly downregulated (P < 0.05). In addition, the activities of NH4+ assimilation enzymes were markedly reduced. This result was further confirmed by the accumulation of NH4+ in root nodules, indicating that the inhibition of nitrogen fixation by HSM may be caused by excessive NH4+ accumulation in root nodules. Furthermore, DEGs involved in flavonoid synthesis, phytohormone biosynthesis, and phytohormone signaling transduction were significantly downregulated (P < 0.05), which was consistent with the decrease in flavonoid and phytohormone contents determined in this study. These results suggested that HSM may inhibit soybean nodulation by inhibiting flavonoid synthesis in soybean roots, disrupting the balance of plant endogenous hormones in roots during symbiosis, and blocking the transmission of hormone signals during the symbiosis. Our findings provide new insights into the effects of HSM on the legume-rhizobium nodule symbiotic process.
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Fabaceae , Rhizobium , Glycine max/genética , Simbiose , Transcriptoma , Reguladores de Crescimento de Plantas , FlavonoidesRESUMO
BACKGROUND: Fall armyworm (FAW, Spodoptera frugiperda) is one of the most destructive and invasive pests worldwide and causes significant economic losses. Intensive and frequent use of insecticides has led to the development of resistance in FAW. Adipokinetic hormone (AKH) have been proven to be involved in insecticide resistance in insects. However, the molecular mechanism underlying chlorantraniliprole resistance mediated by AKH signaling in FAW remains unclear. RESULTS: The expression of SpfAKHR was highest in male adults and lowest in 1st instar larvae. SpfAKH was expressed the highest in eggs and the lowest in 6th instar larvae. AKH signaling was involved in the sensitivity of FAW to chlorantraniliprole through a toxicological bioassay, and the combination of chlorantraniliprole and bithionol (an inhibitor of key enzymes in the AKH pathway) significantly increased the mortality of FAW. Chlorantraniliprole significantly induced the expression of ten P450s, SpfAKH and SpfAKHR in FAW. RNA interference against SpfAKHR significantly decreased the P450 content, downregulated the expression of three P450 genes (SpfCYP6B50, SpfCYP321A9 and SpfCYP9A58) and inhibited the resistance of FAW to chlorantraniliprole. The topical application of AKH peptide significantly increased the P450 content, upregulated the expression of five P450 genes (SpfCYP321A9, SpfCY321A8, SpfCYP321A10, SpfCYP321A7 and SpfCYP6AB12), and enhanced the survival of FAW against chlorantraniliprole. CONCLUSIONS: AKH plays an important role in enhancing chlorantraniliprole resistance in FAW by exerting a positive influence on P450 gene expression and P450 content. These results provide valuable insights into insecticide resistance regulation and FAW control strategies. © 2022 Society of Chemical Industry.
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Inseticidas , Mariposas , Animais , Sistema Enzimático do Citocromo P-450/genética , Sistema Enzimático do Citocromo P-450/metabolismo , Hormônios de Inseto , Resistência a Inseticidas/genética , Inseticidas/farmacologia , Larva , Masculino , Mariposas/metabolismo , Oligopeptídeos , Ácido Pirrolidonocarboxílico/análogos & derivados , Spodoptera , ortoaminobenzoatos/farmacologiaRESUMO
Imazamox (IM) is a chiral pesticide that has been widely used in agriculture. Currently, few studies have investigated the toxicity mechanisms of imazamox to aquatic macrophyte from the enantiomer level. In this study, the enantioselective effects of IM on the toxicity and physiological and biochemical system of aquatic macrophyte Lemna minor were systematically investigated. Metabolomic and transcriptomic for Lemna minor were used to identify potential mechanisms of toxicity. 7 d EC50s for racemic-, R-, and S-IM were 0.036, 0.035, and 0.203 mg/L, respectively, showing enantioselective toxicity. In addition, IM caused Lemna minor lipid peroxidation and antioxidant damage, and inhibited the activities of the target enzymes. Metabolomic and transcriptomic data indicated that R-IM interferenced differentially expressed genes and metabolites of Lemna minor which were enriched in carbon fixation during photosynthesis, glutathione metabolic pathway, pentose phosphate pathway, zeatin biosynthesis, and porphyrin and chlorophyll metabolism. S-IM affected phenylalanine metabolism, phenylpropanoid biosynthesis, zeatin biosynthesis and secondary metabolite biosynthesis. Racemic-IM influenced carbon fixation during operation, glutathione metabolic pathway, zeatin biosynthesis and pentose phosphate pathway. The results provide new insights into the enantioselective toxicity mechanisms of IM to Lemna minor, and lay the foundation for conducting environmental risk assessments.
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Araceae , Transcriptoma , Araceae/genética , Imidazóis , EstereoisomerismoRESUMO
A novel and accurate liquid chromatography-tandem mass spectrometry method was developed to sequentially determine three persistent herbicides (atrazine (ATZ), acetochlor (ACE), and metolachlor (MET)) and seven characteristic metabolites (desethylatrazine (DEA), deisopropylatrazine (DIA), diaminochlorotriazine (DACT), MET-oxanilic acid (MET-OA), MET-ethanesulfonic acid (MET-ESA), ACE-ESA, and ACE-OA) in fresh fish tissues from six fish species. A modified QuEChERS method was conducted to extract the target compounds from fish tissues. Matrix-matched calibrations of the target analytes were carried out at spiking levels of 1, 10, 100, and 1000 ng g-1. The method was validated in accordance with Codex guidelines (CAC/GL 71-2009). Recoveries for the target analytes were 67-120% with relative standard deviations below 20%, and the matrix effects ranged from -58.7% to 59.3%. The limits of detection and quantitation were 0.01-1.90 and 0.02-6.35 ng g-1, respectively. Moreover, the method was successfully applied to analyze the concentrations of the target chemicals in fresh tissue samples of six fish species (n = 67) collected from four markets in Nanning City, Guangxi Province, China. The concentrations in all samples were 1.1-140.5 ng g-1. Interestingly, this study was the first to measure DEA and DIA in fish liver, and their highest concentrations were 10.7 and 14.2 ng g-1, respectively. This method provides a basis for studying the pathways of biotransformation, bioaccumulation, detoxification, and exposure patterns of ACE, ATZ, MET, and their metabolites in aquatic environments.
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Herbicidas , Animais , China , Cromatografia Líquida de Alta Pressão , Cromatografia Líquida , Espectrometria de Massas em TandemRESUMO
The pollution of aquatic environments by microplastics and herbicides has become a global concern. This study was focused on imazamox, imazapic, and imazethapyr sorption to polypropylene microplastics in water. And the potential effects of microplastics on herbicide enantiomer degradation and distributions in water, sediment, and water-sediment microcosms were investigated. Adsorption experiment results indicated that herbicide sorption to microplastics involved both chemisorption and physical adsorption. Degradation experiment results indicated that microplastics could markedly increase herbicide persistence in water and sediment. Marked stereoselective degradation was not found for the three herbicides in water and sediment, but stereoselective degradation of imazapic in water containing microplastics was found. The water-sediment microcosms experiment results indicated that microplastics have significant effect on stereoselectivity degradation and distribution in water and water-sediment microcosms for imazapic, and have little effect on stereoselectivity behaviors of imazamox and imazethapyr in water-sediment systems. Furthermore, the microcosm experiment results also indicated that herbicides can partition between water and microplastics and that microplastics could affect herbicide persistence and distributions in aquatic environments. The present study provides new insights into the fate of chiral pollutants in aquatic environments containing microplastics, and contributes to understanding behaviors of herbicides and microplastics in aquatic environments.
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Herbicidas , Poluentes Químicos da Água , Herbicidas/análise , Microplásticos , Plásticos , Estereoisomerismo , Água , Poluentes Químicos da Água/análiseRESUMO
To reveal the adsorption mechanisms of imazamox, imazapic, and imazethapyr on sediment and batch experiments were carried out in this study. The adsorption kinetics of three imidazolinone herbicides on sediment were accurately described by the pseudo-second-order kinetic model(R2 > 0.9004). The values of adsorption capacity (Qe.cal) were ranged from 0.0183 to 0.0859 mg kg-1 for three herbicides. Adsorption equilibrium was reached within 24 h for three herbicides on sediment, and well fitted by the Freundlich model(R2 > 0.9561). The KF of values for adsorption obtained sediment samples were ranged from 0.2501 to 1.322 L1/n mg1-1/n kg-1for three herbicides. These results indicated that intraparticle diffusion and external mass transport were the main rate controlling steps of the adsorption of herbicides on sediment and that the chemical adsorption was dominant during the adsorption processes. The calculated hysteresis coefficient H were 0.9422,0.7877 and 0.744 for imazmox, imazapic and imazethapyr in raw sediment, respectively, indicating that there is a hysteresis in desorption. The influences of solution pH and sediment organic carbon content on the imidazolinone herbicide adsorption behaviors were also examined. Which shown that the adsorption process for herbicides was highly pH-dependent and adsorption efficiency was closely related to the organic matter content of the sediment, suggesting that electrostatic interactions played crucial roles in the adsorption behavior between sediment and imidazolinone herbicides, and the herbicides were mostly absorbed by the amorphous materials of sediment. These research findings are important for assessing the fate and transport of imidazolinone herbicides in water-sediment systems.
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Herbicidas , Adsorção , Carbono , CinéticaRESUMO
Halosulfuron methyl (HSM) is a herbicide widely used to control sedge and broad-leaved weeds during crop production, but its environmental residue may damage non-target crops. Here, proteomics and metabolomics methods were used to explore the phytotoxicity mechanisms of HSM against soybean (Glycine max Merr.). Soybean seedlings were exposed to 0.01, 0.05 and 0.5 mg/L HSM for 8 d. The HSM applications significantly reduced chlorophyll and carotenoid contents in HSM-treated seedlings. Additionally, chlorophyll a fluorescence was seriously affected. The glutathione, hydrogen peroxide and malondialdehyde contents, as well as antioxidant enzyme activities, significantly increased in seedlings exposed to HSM. Furthermore, five enzymes involved in the tricarboxylic acid (TCA) cycle, α-ketoglutarate dehydrogenase, isocitrate dehydrogenase, aconitase, malic dehydrogenase and succinate dehydrogenase, were inhibited to varying degrees in HSM-treated seedlings compared with controls. Proteomics results showed multiple differentially abundant proteins involved in chlorophyll synthesis, photosystem processes and chloroplast ATP synthetase were down-regulated. Metabolomics analyses revealed that metabolites involved in the TCA cycle decreased significantly. Moreover, metabolites and proteins related to reactive oxygen species detoxification accumulated. In conclusion, the phytotoxicity mechanisms of HSM against soybean mainly act by damaging the photosynthetic machinery, inhibiting chlorophyll synthesis, interrupting the TCA cycle and causing oxidative stress. These results provide new insights into the toxicity mechanisms of sulfonylurea herbicides against non-target crops.
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Glycine max/efeitos dos fármacos , Herbicidas/toxicidade , Plântula/efeitos dos fármacos , Compostos de Sulfonilureia/toxicidade , Clorofila A , Metabolômica , Proteínas de Plantas/fisiologia , Proteômica , Plântula/fisiologia , Glycine max/fisiologiaRESUMO
A simple and reliable analytical method was established for the simultaneous determination of tiafenacil and its six metabolites in fruits. The method involves three steps: extraction using acidified acetonitrile, clean-up by octadecylsilane(C18) and graphitized carbon black (GCB), and detection using liquid chromatography coupled with tandem mass spectrometry (UHPLC-MS/MS). The method was validated on seven matrices spiked at 10, 100 and 1000 µg kg-1. Average recoveries ranged from 73% to 105% with intra-day RSDr (n = 5) of 1.0%-13.0% and inter-day RSDR (n = 15) of 1.1%-14.6%. Good linearities (R2 > 0.9911) were obtained for seven analytes in all matrices. The limit of quantification (LOQs) for tiafenacil and its six metabolites were 10 µg kg-1 in all matrices. This analytical method provides a basis for the establishment of maximum residue limits (MRL) and for the monitoring of tiafenacil residues in fruits.
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Cromatografia Líquida de Alta Pressão/métodos , Contaminação de Alimentos/análise , Frutas/química , Herbicidas/análise , Pirimidinas/análise , Espectrometria de Massas em Tandem/métodos , Acetonitrilas/química , Fracionamento Químico , Análise de Alimentos/métodos , Herbicidas/metabolismo , Limite de Detecção , Reprodutibilidade dos TestesRESUMO
Imidazolinone herbicides are a group of chiral herbicides that are widely used to control weeds in crops. Despite their wide use, few studies on the behavior of enantiomers in terrestrial systems have been reported. In this study, the bioaccumulation of imazamox, imazapic, and imazethapyr enantiomers in earthworm and their degradation in soils were assessed using earthworm-soil microcosms. The bioaccumulation of the three herbicides in earthworm was not significantly enantioselective. Imazamox and imazethapyr did not significant stereoselective degradation in soil (p > 0.05), while the enantioselectivity of the degradation of imazapic was significant (p < 0.05). Furthermore, biota to soil accumulation factor (BSAF) values were also calculated for three herbicides. Relationships between BSAF values and organic matter content of soil and log KOW of herbicides were investigated. The BSAFs values were negatively correlated with the log KOW of herbicides, and were positively correlated with organic matter content of soil in earthworm-soil microcosms. These relationships indicated that chemical hydrophobicity (Kow) and organic matter content of soil were good predictors to estimate the bioavailability of imidazolinone herbicides to earthworm.
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Oligoquetos , Animais , Bioacumulação , Herbicidas , Solo , Poluentes do Solo , EstereoisomerismoRESUMO
Sublethal exposure to neonicotinoids affects honey bee olfaction, but few studies have investigated the sublethal effects of the enantioselective neonicotinoid dinotefuran on honey bee olfaction. This study assessed the sublethal olfactory toxicity of dinotefuran enantiomers to honey bees. Compared to R-dinotefuran, S-dinotefuran had higher acute oral toxicity, sucrose sensitivity effects, octopamine concentrations, lower learning ability, and memory effects on honey bees. High-throughput circular RNA sequencing of the honey bee brain revealed that R-dinotefuran caused more gene regulatory changes than S-dinotefuran. Gene ontology enrichment and Kyoto Encyclopedia of Genes and Genomes pathway analyses demonstrated that the SERCA, Kca, and Maxik genes may be related to the enantioselective effects of dinotefuran isomers on honey bee olfaction. These results indicated that the current ecotoxicological safety knowledge about chiral dinotefuran effects on honey bees should be amended.
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Abelhas/efeitos dos fármacos , Guanidinas/toxicidade , Inseticidas/química , Inseticidas/toxicidade , Neonicotinoides/toxicidade , Nitrocompostos/toxicidade , Animais , Abelhas/fisiologia , Guanidinas/química , Neonicotinoides/química , Nitrocompostos/química , Olfato/efeitos dos fármacos , EstereoisomerismoRESUMO
A simple and efficient multiresidue method using dispersive solid phase extraction and liquid chromatography coupled with tandem mass spectrometry was developed for the targeted analysis of indaziflam and its five metabolites (indaziflam-diaminotriazine, indaziflam-carboxylic acid, indaziflam-triazine indanone, indaziflam-hydroxyethyl, and indaziflam-olefin) in pitaya samples (including roots, plants, flowers, peels, pulp, and whole fruit). The analytes were extracted with acetonitrile, and the extracts were purified using multiwalled carbon nanotubes. The method was validated using pitaya samples spiked at 0.5, 5, and 50 µg/kg, and the average recoveries varied from 61.1 to 103.7% with relative standard deviations lower than 12.7% (n = 5). This method exhibited sufficient linearity within the concentration range of 0.1-100 µg/L. The limits of detection and quantification were in the ranges of 0.001-0.1 and 0.003-0.3 µg/kg, respectively. The method was successfully applied to analyze pitaya samples in Nanning, and no indaziflam or its metabolites were detected in the samples analyzed.
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Cactaceae/química , Indenos/análise , Extração em Fase Sólida , Triazinas/análise , Cromatografia Líquida de Alta Pressão , Frutas/química , Frutas/metabolismo , Indenos/metabolismo , Espectrometria de Massas em Tandem , Triazinas/metabolismoRESUMO
Hydrolysis and photolysis of bentazone in abiotic aqueous solutions were examined under laboratory conditions. Hydrolysis was studied in different buffer solutions (pH 4.0 ± 0.1, 7.0 ± 0.1, and 9.0 ± 0.1), at different temperatures (15 °C ± 2 °C, 25 °C ± 2 °C, 35 °C ± 2 °C, and 45 °C ± 2 °C), and at different Fe3+ concentrations (1, 5, and 10 mg/L). Photolysis was assessed in different buffer solutions and at different solvent (methanol and ethyl acetate) concentrations (10%, 20%, and 30%) or Fe3+ (1, 5, and 10 mg/L) concentrations and under mercury or xenon light irradiation. Hydrolysis half-lives ranged 46-99 days at three different conditions. Photolysis half-lives ranged 2.3-7.5 h in three different conditions under mercury and xenon irradiation. Hydrolysis and photolysis of bentazone were accelerated by both alkaline conditions and elevated temperatures, and solvents and Fe3+ strongly enhanced bentazone degradation. Photodecomposition was much faster under a mercury lamp than under a xenon lamp. N-methyl bentazone and 6-OH bentazone/8-OH bentazone were identified as degradation products using UPLC-Q-TOF-MS. The data generated from this study could be useful for risk assessment of pesticides in the environment.
Assuntos
Benzotiadiazinas/química , Poluentes Químicos da Água/química , Hidrólise , Espectrometria de Massas , Fotólise , Solventes , Água/química , Poluentes Químicos da Água/análiseRESUMO
This study aimed to investigate the potential use of water hyacinth (Eichhornia crassipes) in removing two herbicides (mesotrione and fomesafen) with long degradation cycles in water. The relative growth rate (RGR) of water hyacinth in the presence of 100-mg/L mesotrione and fomesafen was significantly lower than that in their absence, particularly with fomesafen. Moreover, the RGRFW and RGRDW with treatment with fomesafen were 1.47- and 1.58-fold lower than those with treatment with mesotrione, respectively. The disappearance rate constants of mesotrione and fomesafen in natural water were, respectively, 0.1148 and 0.0276 d-1 with plants and 0.0038 and 0.0005 d-1 without plants. The disappearance rate constants with and without plants were significantly different, indicating that uptake by plants combined with degradation by plant-associated bacteria account for 96.7% and 98.2% of the removal of mesotrione and fomesafen, respectively. The bioconcentration factor for mesotrione and fomesafen in living water hyacinth plants ranged 0.38-16.97 and 1.05-3.50 L/kg, respectively, whereas the residues of mesotrione and fomesafen in water decreased by 70-92 and 22-34%, respectively, after the plants were grown for 14 d in culture solution with 100-mg/L mesotrione and fomesafen. These results show that uptake by plants combined with degradation by plant-associated bacteria may be the dominant process in the removal of mesotrione and fomesafen from water by plants. Water hyacinth may be applied as an efficient, economical, and ecological alternative to accelerate the removal and degradation of agro-industrial waste water polluted with mesotrione and fomesafen.