Two sampling strategies for an overview of pesticide contamination in an agriculture-extensive headwater stream

Two headwaters located in southwest France were monitored for 3 and 2 years (Auvézère and Aixette watershed, respectively) with two sampling strategies: grab and passive sampling with polar organic chemical integrative sampler (POCIS). These watersheds are rural and characterized by agricultural areas with similar breeding practices, except that the Auvézère watershed contains apple production for agricultural diversification and the downstream portion of the Aixette watershed is in a peri-urban area. The agricultural activities of both are extensive, i.e., with limited supply of fertilizer and pesticides. The sampling strategies used here give specific information: grab samples for higher pesticide content and POCIS for contamination background noise and number of compounds found. Agricultural catchments in small headwater streams are characterized by a background noise of pesticide contamination in the range of 20–70 ng/L, but there may also be transient and high-peak pesticide contamination (2000–3000 ng/L) caused by rain events, poor use of pesticides, and/or the small size of the water body. This study demonstrates that between two specific runoff events, contamination was low; hence the importance of passive sampler use. While the peak pesticide concentrations seen here are a toxicity risk for aquatic life, the pesticide background noise of single compounds do not pose obvious acute nor chronic risks; however, this study did not consider the risk from synergistic “cocktail” effects. Proper tools and sampling strategies may link watershed activities (agricultural, non-agricultural) to pesticides detected in the water, and data from both grab and passive samples can contribute to discussions on environmental effects in headwaters, an area of great importance for biodiversity.     

垃圾焚烧中氯化物对重金属Cd迁移转化特性的影响

采用管式炉和模拟垃圾对垃圾焚烧中氯化物对重金属Cd迁移转化特性的影响进行了研究,使用ICP-AES(美国EPA消解方法)、SEM、EDS和XRD分析技术对重金属浓度、灰渣表面形貌、成分和灰渣X射线衍射物相等进行了分析.结果表明,氯化物的加入均使得97％以上的Cd分布于飞灰中,且随氯化物含量的增加在飞灰中的分布逐渐增加.有机氯PVC和无机氯NaCl含量的变化对Cd迁移分布的影响没有显著差别.PVC对Cd迁移分布影响受温度影响显著,550℃时Cd在飞灰中分布为80.51%,850℃时Cd在飞灰中的分布上升为97.91%,但在温度超过CdCl₂的熔点568℃后温度的影响较小.NaCl对Cd的迁移分布受温度影响不明显,加入NaCl后550℃时Cd在飞灰中分布为95.02%,1 000℃时在飞灰中的分布为96.58%.氯化物存在下停留时间对Cd迁移分布没有显著影响.底渣和飞灰的SEM/EDS和XRD分析表明,PVC和NaCl对Cd迁移转化作用机理不同.     

咪唑型离子液体对小鼠的急性毒性

采用寇氏改良法研究了咪唑型离子液体对小鼠的急性毒性,并考察了烷基侧链长度对其毒性的影响,同时采用HE染色法观察了其对小鼠肝脏的毒性.结果表明,4种咪唑型离子液体([C10mim]Br、[C12mim]Br、[C14mim]Br和[C18mim]Br)对小鼠肝脏均有损伤,其LD50值在98.91～220.16 mg·kg...     

Potential impacts of climate change on agricultural land use suitability of the Hungarian counties

Central and Eastern European countries are a hotspot area when analyzing the impacts of climate change on agricultural and environmental sectors. This paper conducts a socio-economic evaluation of climate risks on crop production in Hungary, using panel data models. The region has a special location in the Carpathian basin, where the spatial distribution of precipitation varies highly from humid conditions in the western part to semiarid conditions in eastern Hungary. Under current conditions, crop systems are mainly rainfed, and water licences are massively underexploited. However, water stress projected by climate change scenarios could completely change this situation. In the near future (2021–2050), most of the crops examined could have better climatic conditions, while at the end of the century (2071–2100), lower yields are expected. Adaptation strategies must be based on an integrated evaluation which links economic and climatic aspects, and since the results show important differences in the case of individual systems, it is clear that the response has to be crop and region specific.     

基于“径流-地类”参数的非点源氮磷负荷估算方法

东江作为广东省重要的饮用水源,其上游农业集水区非点源氮磷流失量备受关注.因此,本文以东江上游上莞河小流域为研究区,利用2011年的集水区水质监测数据,在平均浓度法及输出系数法的基础上,构建基于"径流-地类"参数的非点源氮磷负荷计算式,其径流、地类参数分别通过校正后的SCS模型和土地利用现状图获取,并分别对上莞河流域及流域各地类的非点源氮磷流失量进行估算.研究结果表明,汛期上莞河流域氮磷流失量主要来源于非点源污染,其非点源氮、磷流失量分别占氮、磷流失总量的97.32%、98.05%.坡度对流域非点源氮磷流失影响较小,地类是影响非点源氮磷输出的重要因素.构建的计算式能较好地估算非点源氮、磷负荷量,在次暴雨尺度非点源氮、磷输出量模拟精度分别为84.78%、81.06%.2011年度上莞河流域非点源氮、磷输出量分别为48923.4、7189.3 kg,耕地、居民地分别是非点源氮、磷输出的关键源区,其非点源氮、磷输出量分别占流域非点源氮、磷输出总量的84.20%、58.54%.     

低温短时水热预处理混合及初沉污泥的高温厌氧消化特性研究

以低温短时(90℃、30 min)水热预处理后的混合及初沉污泥为研究对象,分别进行了高温((55±1)℃)厌氧消化连续性试验.研究了该预处理条件下这两类污泥在水力停留时间(HRT)为20 d时的产气量、有机物分解率及物料平衡等,探讨了低温短时水热预处理对提高污泥厌氧消化性能的效果.结果表明:TS约为35 g·L-1的预处理混合污泥与初沉污泥经高温厌氧消化后,投加单位VS的产气量分别为(343.00±9.86)m L·g-1和(365.00±7.61)m L·g-1,VS去除率分别为38.9%和45.8%.COD物料平衡计算结果表明,混合和初沉污泥中分别有33.6%和43.9%的固体有机物被分解转化,生物气中CH4含量均在70%左右.     

电化学氧化PFOA阳极材料筛选及其机制研究

全氟辛酸(PFOA)具有环境持久性及内分泌干扰性,传统的生物降解及高级氧化法对PFOA的去除效果微弱.本研究采用电化学氧化法降解PFOA,选取BDD(掺硼金刚石电极)、Pt、Ti、Ti/RuO2、Ti/RuO2-IrO2、Ti/In2O3、Ti/SnO2-Sb2O5-IrO2、Ti/SnO2-Sb2O5-RhO2、Ti/SnO2-Sb2O5、Ti/SnO2-Sb2O5-CeO2和Ti/SnO2-Sb2O5-Bi2O3这11种阳极材料为备选电极.采用线性扫描伏安法测试析氧电位(OEP),评价11种电极对PFOA的降解效果和脱氟效果,并采用超声-电化学协同方法间接证明PFOA分子在电极表面的直接电子转移是降解反应的第一步.Ti/SnO2-Sb2O5-Bi2O3、Ti/SnO2-Sb2O5-CeO2、Ti/SnO2-Sb2O5和BDD对PFOA有较好的电氧化效果,降解率分别是89.8%、89.8%、93.3%和98.0%.Pt、Ti/SnO2-Sb2O5-RhO2、Ti/SnO2-Sb2O5-IrO2和Ti/In2O3对PFOA的电氧化效果微弱,降解率分别是2.1%、2.3%、12.5%和3.1%.而Ti、Ti/RuO2和Ti/RuO2-IrO2对PFOA没有电氧化能力.PFOA分子经过电极表面的直接电化学氧化发生脱羧反应,后经过逐步脱掉CF2单元的循环生成短链的全氟羧酸类化合物C6F13COO-、C5F11COO-、C4F9COO-和C3F7COO-.     

Remobilization of polychlorinated biphenyls from sediment and its consequences for their transport in river waters

A laboratory experiment was performed to examine the remobilization of indicator polychlorinated biphenyls (iPCBs) from sediments and its results were applied to the real-world data for explaining the transport of PCBs in river. Seven PCB concentrations were determined in three series of model water–sediment systems (3 g of river sediment, three different volumes of distilled water (0.5, 0.25, and 0.15 ml), and 5 mg of biocide) after 11 days of incubation. Solid-phase extraction was used for separation of analytes from the aqueous phase and solvent extraction for isolation of analytes from the sediments, respectively. The extracts were analyzed for individual iPCB congeners using gas chromatography–mass spectrometry method. For each series of the experiment, the concentrations of PCBs in aqueous phase were similar. The average sediment/water partition coefficient value was 10⁴?l/kg. The solubility of individual PCB congeners in water did not influence the desorption of PCBs from the sediment. Although the dominant form of PCBs in a water–sediment system occurs as suspended and colloidal fractions, these compounds are transported mostly in a dissolved form. Suspended and colloidal matter is a major sink for PCBs in low-energy aquatic environments. In contrast, the dissolved PCBs are readily transported in running waters. The mobilization of PCBs from sediments to aqueous phase, with respect to their solubility in water, seems to be limited, thus reducing the risk of secondary pollution.     

改性沸石分离富集-火焰原子吸收光谱法测定长江水中镉

采用改性沸石分离富集-火焰原子吸收光谱法测定长江水中微量镉,优化了富集和洗脱条件,讨论了干扰离子的影响。方法在0μg~4.00μg范围内线性良好,检出限为0.214μg/L,长江水平行测定的RSD为1.8%,加标回收率为99.0%~104%。