中草药提取物对致病弧菌抑菌活性的筛选

为了寻找高效植物源杀菌剂,实验采用平板扩散法研究了8种中草药醇提物对致鱼病菌的体外抑菌试验。通过双倍试管稀释法,测定了最小抑菌浓度(MIC)和最低杀菌浓度(MBC)。结果显示,这8种中草药醇提物对致病弧菌均有不同程度的抑制作用,其中以臭椿和盐肤木醇提物对所有供试菌均有较高的抑制活性,臭椿醇提物对病菌的MIC均在7.81mg/mL以下,表明中草药杀菌剂具有较高的开发价值和应用前景。     

Assessing the impact of fungicide enostroburin application on bacterial community in wheat phyllosphere

Fungicides have been used extensively for controlling fungal pathogens of plants. However, little is known regarding the effects that fungicides upon the indigenous bacterial communities within the plant phyllosphere. The aims of this study were to assess the impact of fungicide enostroburin upon bacterial communities in wheat phyllosphere. Culture-independent methodologies of 16S rDNA clone library and 16S rDNA directed polymerase chain reaction with denaturing gradient gel electrophoresis (PCR-DGGE) were used for monitoring the change of bacterial community. The 16S rDNA clone library and PCR-DGGE analysis both confirmed the microbial community of wheat plant phyllosphere were predominantly of the γ-Proteobacteria phyla. Results from PCR-DGGE analysis indicated a significant change in bacterial community structure within the phyllosphere following fungicide enostroburin application. Bands sequenced within control cultures were predominantly of Pseudomonas genus, but those bands sequenced in the treated samples were predominantly strains of Pantoea genus and Pseudomonas genus. Of interest was the appearance of two DGGE bands following fungicide treatment, one of which had sequence similarities (98%) to Pantoea sp. which might be a competitor of plant pathogens. This study revealed the wheat phyllosphere bacterial community composition and a shift in the bacterial community following fungicide enostroburin application.     

4种甲氧基丙烯酸酯类杀菌剂不同剂型对斑马鱼急性毒性效应

采用半静态法测定了4种甲氧基丙烯酸酯类杀菌剂原药及制剂对斑马鱼(Brachydonio rerio)急性毒性。结果表明,以实测浓度计,250 g·L~(-1)嘧菌酯悬浮剂对斑马鱼的96 h半数致死浓度(LC50)值为0.539 mg·L~(-1),急性毒性为高毒,95%嘧菌酯原药和50%嘧菌酯水分散粒剂对斑马鱼的LC50(96 h)值分别为1.09和1.21 mg·L~(-1),急性毒性均为中毒;98%啶氧菌酯原药和22.5%的啶氧菌酯悬浮剂对斑马鱼的LC50(96 h)值分别为0.0974和0.0972 mg·L~(-1),急性毒性均为剧毒;95%吡唑醚菌酯原药、15%吡唑醚菌酯悬浮剂和250 g·L~(-1)吡唑醚菌酯乳油对斑马鱼的LC50(96 h)值为0.0613、0.0549和0.0487 mg·L~(-1),急性毒性均为剧毒;95%醚菌酯原药和50%醚菌酯水分散粒剂对斑马鱼的LC50(96 h)值分别为0.468和0.702 mg·L~(-1),急性毒性均为高毒。这4种甲氧基丙烯酸酯类杀菌剂对斑马鱼均有较高风险,会对其他水生生物也存在潜在的风险。     

杀菌剂叶青双在水中的降解特性研究

提出了一种检测水中叶青双及其降解物２－氨基－５－巯基－１,３,４－噻二唑的反相高效液相色谱分析法,进行了叶青双的水解、光解以及池塘水中自然降解的模拟试验。研究表明：叶青双在水中降解非常快,光解是其降解的主要方式,同时水解也对叶青双的降解有很大贡献。从叶青双的主要降解产物在水中的光解以及叶青双在自然池塘中模拟试验来看,叶青双的降解产物在水中也不稳定。由此得出叶青双在稻区正常使用情况下,不会对水环境及鱼类构成威胁的结论。     

Development of competitive immunoassays to hydroxyl containing fungicide metabolites

This paper describes the isolation of monoclonal antibodies and the development of competitive immunoassays to pesticide metabolites of the fungicides imazalil, carbendazim and thiabendazole. The metabolite specific hydroxyl residues were used as the reactive group with which to link the metabolite to the carrier proteins Keyhole Limpet Haemocyanin (KLH) and Bovine Serum Albumin (BSA). In each case immune responses in mice were raised and monoclonal antibodies were produced. Antibodies were developed into competitive ELISAs to the appropriate metabolite. The antibody raised to a metabolite of imazalil was optimised into a competitive ELISA format which had an assay IC50 of 7.5 μg/L and a limit of detection (LOD) of 1.1 μg/L. A single antibody isolated against the metabolite of carbendazim had assay IC50s of 3.2 and 2.7 μg/L for the metabolites of carbendazim and thiabendazole respectively with an LOD of 0.38 μg/L for both. These sensitive immunoassays may have application in the monitoring of human exposure to these fungicide residues either by occupational or non-occupational routes.     

Residue analysis and dissipation of a new fungicide 2-allylphenol in tomato

Introduction 2 allylphenol with commercial name of LuDi, is a newfungicide developed and synthesized by the AgriculturalEngineering Research Center(China), which simulated theactive compound structure in Gingko (Gingko biloba L.).The field trial…     

21种杀菌剂对家蚕的急性毒性与风险评价

旨在为桑园及周围农田合理选择和使用农药提供科学依据,采用食下毒叶法测定了农业生产上常用的21种杀菌剂对家蚕的急性毒性,并进行了风险评价.急性毒性测定结果表明:20％苯醚甲环唑微乳剂、10％氟硅唑水乳剂、12.5％腈菌唑水乳剂、12.5％烯唑醇可湿性粉剂和70％嗯霉灵可湿性粉剂对家蚕的96 h-LC50值为46.5(41...     

Comparative quantitative structure–activity relationship (QSAR) study on acute toxicity of triazole fungicides to zebrafish

We employed two-dimensional quantitative structure–activity relationship (2D-QSAR) and hologram QSAR (HQSAR) methods to quantitatively investigate the mechanism and active site of toxicity for Danio rerio exposed to triazole fungicides. Our results showed that 2D-QSAR models constructed using the energy of the lowest unoccupied molecular orbit, the net C atom charges, the octanol–water partition coefficient and the molecular shape factor had higher predictive abilities. HQSAR models containing the fragment distinctions atoms (As), bonds (Bs), chirality (Ch) and donors and acceptors (D&A) had higher reliability. It was found that 2D-QSAR results explaining the toxicity mechanism were consistent with HQSAR. In summary, the hydrophobicity and shape/size of the molecule were the important factors influencing the toxic effect of these chemicals against D. rerio. In addition, electron exchange may occur between these fungicides and the target. The study provided a method to evaluate the environmental risk of chemicals with a similar structure, based on the QSAR models obtained.     

Effects of chlorothalonil and carbendazim on nitrification and denitrification in soils

The effects of chlorothalonil and carbendazim on nitrification and denitrification in six soils in upland and rice paddy environments were investigated. Laboratory aerobic (60% water holding capacity) and anaerobic (flooded) conditions were studied at 25°C and fungicide addition rates of 5.5 mg/kg A. I. (field rate, FR), 20 times (20FR) and 40 times (40FR) field rate, respectively. The results indicated that chlorothalonil at the field rate had a slight inhibitory effect on one soil only, and that soil did ...     

4种甲氧基丙烯酸酯类杀菌剂对拟澳洲赤眼蜂成蜂的急性毒性及安全性评价

为甲氧基丙烯酸酯类杀菌剂合理使用提供科学依据,本研究采用试管药膜法测定了啶氧菌酯、吡唑醚菌酯、嘧菌酯和醚菌酯等4种药剂的原药及其制剂对拟澳洲赤眼蜂成蜂的急性毒性,并进行了安全性评价。对比原药结果发现,啶氧菌酯原药和醚菌酯原药毒性很高,LR50依次是2.66×10-4及7.32×10-4mg a.i.·cm~(-2),均属于高风险;而吡唑醚菌酯原药及嘧菌酯原药毒性较低,LR50分别为3.01×10-3和3.47×10-3mg a.i.·cm~(-2),均为中等风险药剂。对比制剂结果发现,啶氧菌酯悬浮剂毒性最高,LR50为5.02×10-5mg a.i.·cm~(-2),为极高风险药剂;其次是吡唑醚菌酯悬浮剂及乳油,LR50分别为3.78×10-3和5.80×10-3mg a.i.·cm~(-2),均为中等风险药剂;最低的是嘧菌酯水分散粒剂、悬浮剂和醚菌酯水分散粒剂,LR50均大于4.0×10-2mg a.i.·cm~(-2),均为低风险药剂。部分甲氧基丙烯酸酯类杀菌剂对天敌赤眼蜂存在较高风险,特别是啶氧菌酯,应避免田间使用,或通过避开赤眼蜂释放期来减少对赤眼蜂的伤害。