SMBBR-AF-SMBBR组合工艺处理高氨氮农药废水

采用特异性移动床生物膜反应器(SMBBR)和厌氧生物滤池(AF)组合工艺处理高氨氮农药废水。考察了HRT、pH和DO等工艺条件对SMBBR-AF-SMBBR组合工艺运行稳定期COD和氨氮去除率的影响。试验结果表明,在进水COD为2 408~7 440 mg/L、ρ(NH_4~+-N)为160.21~433.84 mg/L、TN为208.27~537.65 mg/L、HRT为8d、pH为8.0、DO为4 mg/L的条件下,处理后出水平均COD为342 mg/L,COD去除率达92.3%;ρ(NH_4~+-N)小于4.0mg/L,氨氮平均去除率为89.2%;TN小于50 mg/L,平均TN去除达83.0%。出水各指标均优于原A2O工艺出水。     

新烟碱类农药的污染现状及转化行为研究进展

新烟碱类(neonicotinoids)农药自在20世纪80年代中期引入以来,便发展成为世界上使用最广泛的一类杀虫剂。近年来,该类化合物在环境中被不断检出,并通过饮用水和食物等方式进入食物链,给人类健康带来极大的安全隐患。文章综述了新烟碱类杀虫剂在空气、土壤、水相、生物体和人体中的暴露浓度,以及这类农药在环境中的转化行为。目前针对新烟碱类杀虫剂的环境暴露研究仍十分有限,需要更全面调查其在多环境介质中的暴露状况以综合评价其生态风险。关于新烟碱类化合物的毒理学研究主要集中在急性毒性试验,而对于其他形式的毒性效应有待进一步研究。最后对新烟碱农药未来的研究重点和方向提出了展望。     

气相色谱-质谱法测定沉积物中的有机氯和多氯联苯

采用加速溶剂萃取法提取沉积物中的有机氯和多氯联苯,提取液用凝胶色谱法净化后用气相色谱-质谱法测定。方法在5.00μg/L~200μg/L范围内线性良好,当取样量为10.0 g时,方法检出限为0.03μg/kg~0.37μg/kg,空白样品2个质量比水平的加标回收率为70.8%~121%,测定结果的RSD为2.7%~11.5%。用该方法测定实际样品,结果 12个抽检的沉积物样品中多氯联苯均未检出,9个样品中有机氯检出。     

Human milk contamination by nine organochlorine pesticide residues (OCPs)

Abstract

Organochlorine pesticides (OCPs) are widely used around the world as insecticides, herbicides, fungicides, nematicides, and rodenticides. Despite banned in Brazil, the usage remains occurring in many countries. The persistence and extreme mobility of OCPs contribute to the contamination of the environment and the human body. The OCPs bioaccumulation in adipose tissue triggers the excretion into human milk during breastfeeding. Hence, the present study determined eighteen OCPs residues in the breast milk of mothers from the Western Region of Bahia State, Brazil. Nine different residue species were found, including beta-Hexachlorocyclohexane (9.24?±?0.00?ng g^?1 fat), delta- Hexachlorocyclohexane (22.15?±?10.48?ng g^?1 fat), Heptachlor (58.08?±?74.13?ng g^?1 fat), Aldrin (142.65?±?50.65?ng g^?1 fat), Dieldrin (774.62?±?472.68?ng g^?1 fat), Endosulfan I (408.44?±?245.51?ng g^?1 fat), Dichloro-diphenyl-dichloro-ethylene (29.17?±?22.42?ng g^?1 fat), Dichloro-diphenyl-trichloro-ethane (28.87?±?0.00?ng g^?1 fat) and Methoxychlor (1699.67?±?797.43?ng g^?1 fat). The Methoxychlor presence in all samples may reveal a recent exposure, while Dieldrin and Endosulfan I analyses can point to distant past exposure.     

气相色谱法测定土壤中37种有机磷农药残留

采用气相色谱法测定土壤中37种有机磷农药,当取样量为10 g时,37种有机磷农药方法检出限为0. 002～0. 015 mg/kg,测定下限为0. 008～0. 060 mg/kg。低含量加标样品中有机磷农药的加标回收率为72. 8%～104%,相对标准偏差为4. 2%～13. 8%;中含量加标样品中有机磷农药的加标回收率为71. 5%～101%,相对标准偏差为4. 3%～13. 5%;高含量加标样品中有机磷农药的加标回收率为74. 6%～109%,相对标准偏差为6. 8%～14. 6%。该方法灵敏度高、分离效果好、重现性好,能够满足土壤中37种有机磷农药残留检测的要求。     

液液萃取-气相色谱法测定地表水中17种有机氯农药研究

建立了二氯甲烷液液萃取-气相色谱法同时测定地表水中17种有机氯农药的方法。标准曲线线性良好,17种化合物的相关系数R2均大于0.999。当取样量为200 mL时,方法检出限在0.015μg/L~0.062μg/L之间。以超纯水样品进行基质加标实验,重复测定6次的相对标准偏差为1.2%~6.2%,平均加标回收率为72.8%~93.5%。方法简单快捷,精密度良好,准确性高,适用于地表水中痕量有机氯农药的测定。     

通用浓度加和模型预测有机磷与三嗪农药对绿藻的联合毒性

基于微板藻毒性试验测定5个有机磷农药与4个三嗪类农药的单个及联合毒性.根据半数效应浓度(EC50),对斜生栅藻96h生长抑制的毒性大小顺序为:西草净>阿特拉津>扑灭通>苯嗪草酮>草甘膦>敌敌畏>磷胺>乙酰甲胺磷>甲胺磷.这表明直接干扰光合作用电子传输的三嗪除草剂的藻毒性明显大于有机磷农药.以通用浓度加和作为参考模型,三嗪类农药按EC50和EC10(10%效应浓度)浓度比的混合物对斜生栅藻呈现加和毒性.有机磷农药按EC50和EC10浓度比的混合物在低浓度呈现加和毒性,在高浓度呈现协同毒性.有机磷与三嗪类农药按EC50和EC10浓度比的混合物在低浓度为加和毒性,在高浓度为协同毒性.     

Toxicity of pesticides toward human immune cells U-937 and HL-60

Abstract

The industrialization of the agricultural sector has significantly increased the use of chemicals such as pesticides. Therefore, exposure to them is unavoidable, which makes it necessary to assess their safety for humans at actual exposure doses. This paper aims to determine toxicity of three types of pesticides toward human immune cells (HL-60 and U-937): glyphosate (GLY), deltamethrin (DEL), and chlorothalonil (CHL). Cell viability, membrane integrity, inflammation induction, and antioxidant activity were evaluated to determine differences in cellular response to the tested plant protection agents. In experimental models, all tested substances caused increased mortality of cells after only 24?h. Cell membrane damage was recorded under DEL and CHL influences. The largest disintegration of the cell membrane was due to the action of 100?μg/mL DEL for U-937 and CHL at 1?μg/mL for HL-60. GLY at a concentration of 3,600?μg/mL caused significant peroxidation of U-937 cells’ lipids. CHL-induced inflammation in both types of cells tested. DEL and GLY also induced antioxidant activity in cells. These results lead to the conclusion that the tested pesticides act cytotoxically to the cells of the human immune system in doses to which both farmers and consumers are exposed.     

有机磷农药对蛋白核小球藻的毒性相互作用研究

水体中农药复合污染产生的毒性效应具有潜在风险。为系统考察有机磷农药(OPs)混合物对淡水生态系统中绿藻的联合毒性效应,以马拉硫磷(MIT)、敌敌畏(DDVP)、敌百虫(TRC)、乐果(DIT)和氧乐果(OMT)等5种OPs作为混合物组分,运用直接均分射线法设计9组二元混合物体系共45条混合物射线。利用96孔微板测定5种OPs及其二元混合物对蛋白核小球藻(C. pyrenoidosa)的生长抑制毒性,通过基于置信区间的组合指数法分析混合物的联合毒性及毒性相互作用。结果表明,以p EC50为毒性指标,5种OPs对C. pyrenoidosa的毒性大小顺序为:TRCMITDDVPOMTDIT,OPs对C. pyrenoidosa的毒性大小受其中心磷原子的电正性影响;因混合组分的不同,部分OPs混合物对C. pyrenoidosa的联合毒性依赖于组分浓度比; OPs混合物对C. pyrenoidosa的毒性相互作用以加和为主,部分发生拮抗作用,发生拮抗作用的混合体系具有低效应区域呈加和作用,高效应区域呈拮抗作用的规律;与MIT混合的体系均有发生拮抗作用,且依赖于MIT浓度,MIT浓度比例越高,拮抗作用越强,OPs混合物的毒性相互作用与组分浓度比相关; OPs混合物的毒性相互作用组分浓度比依赖性与其联合毒性的组分浓度比依赖性规律不相关。     

Variability of pesticide residues in cauliflower units collected from a field trial and market places in Greece

To estimate the variability of pesticide residue levels present in cauliflower units, a total of 142 samples were collected from a field trial of a cooperative farmer, and 120 samples were collected from different market places in Thessaloniki, Greece. The collected samples were extracted using the quick, easy, cheap, effective, rugged, and safe (QuEChERS) extraction technique, and the residues were determined by liquid chromatography–tandem mass spectrometry. The developed method was validated by evaluating the accuracy, precision, linearity, limit of detection (LOD), and limit of quantification (LOQ). The average recoveries for all the analytes, derived from the data of control samples fortified at 0.01, 0.05, 0.1, and 0.2 mg/kg, ranged from 74 to 110% with a relative standard deviation of ≤8%. The correlation coefficient (R²) was ≥0.997 for all the analytes using matrix-matched calibration standards. The LOD values ranged from 0.001 to 0.003 mg/kg, and the LOQ was determined at 0.01 mg/kg for all the sought analytes. The matrix effect was found to be at a considerable level, especially for cypermethrin and deltamethrin, amounting to +90% and +145%, respectively. For the field samples, the unit-to-unit variability factors (VFs) calculated for cypermethrin and deltamethrin were 2.38 and 2.32, respectively, while the average VF for the market basket samples was 5.11. In the market basket samples, residues of cypermethrin, deltamethrin, chlorpyrifos, and indoxacarb were found at levels ≥LOQ and their respective VFs were 7.12, 5.67, 5.28, and 2.40.