贵州红枫湖大冲小流域农业面源污染负荷特征研究

为揭示红枫湖汇水区农业面源污染物氮、磷、有机物输出的一般规律,以典型农业小流域为研究对象,自2010年1~12月,对流域降雨、流域出口的径流、TN、TP、CODcr浓度进行同步监测,并对流域内各个不同土地利用类型的产污负荷进行监测分析。结果表明,流域除TP外,其他指标严重超标;监测期间小流域径流量为414×105 m3,TN、TP、CODcr入湖总量分别为2 5467、856、10 8832 kg,其日均单位排放负荷分别为577、019 、1451 kg/(km2·d);在降雨丰富、农业生产活动频繁的6~10月,TN、TP、CODcr的含量都明显高于其他月份,分别占各自总量的94.8%、73.3%、94.3%;坡耕地、天然林、疏林地产生的TN、TP、CODcr污染负荷量分别为流域入湖污染总负荷的13.38%、13.29%、13.54%,稻田、蔬菜地径流中TN、TP、CODcr含量分别为0.84~10.32、0.07~0.18、20.50~68.00;2.16~7.54、0.01~0.04、4.50~22.40 mg/L。居民生活污水中TN、TP、CODcr含量分别为13.84~50.11、3.20~5.10、35.7~207.0 mg/L,蔬菜、水稻种植、居民生活污水及禽畜养殖对流域面源污染贡献大;大冲小流域面源污染负荷与径流间存在极强的相关性     

考虑滑移的锈蚀混凝土偏压构件抗弯刚度模型

对锈蚀混凝土偏压构件抗弯刚度退化的影响因素进行了研究,采用刚度解析法对粘结性能退化后偏压构件的截面刚度进行了理论分析,引入了锈蚀钢筋滑移的粘结退化综合影响系数,建立了考虑滑移的锈蚀钢筋混凝土偏压构件抗弯刚度的计算模型。经试验验证,模型的抗弯刚度计算值与试验实测值结果吻合较好,故模型计算值可为锈蚀混凝土偏心受压构件性能的评估提供参考。     

Degradation of ethylenethiourea pesticide metabolite from water by photocatalytic processes

In this study, photocatalytic (photo-Fenton and H₂O₂/UV) and dark Fenton processes were used to remove ethylenethiourea (ETU) from water. The experiments were conducted in a photo-reactor with an 80 W mercury vapor lamp. The mineralization of ETU was determined by total organic carbon analysis, and ETU degradation was qualitatively monitored by the reduction of UV absorbance at 232 nm. A higher mineralization efficiency was obtained by using the photo-peroxidation process (UV/H₂O₂). Approximately 77% of ETU was mineralized within 120 min of the reaction using [H₂O₂]₀ = 400 mg L^?1. The photo-Fenton process mineralized 70% of the ETU with [H₂O₂]₀ = 800 mg L^?1 and [Fe²⁺] = 400 mg L^?1, and there is evidence that hydrogen peroxide was the limiting reagent in the reaction because it was rapidly consumed. Moreover, increasing the concentration of H₂O₂ from 800 mg L^?1 to 1200 mg L^?1 did not enhance the degradation of ETU. Kinetics studies revealed that the pseudo-second-order model best fit the experimental conditions. The k values for the UV/H₂O₂ and photo-Fenton processes were determined to be 6.2 × 10^?4 mg L^?1 min^?1 and 7.7 × 10^?4 mg L^?1 min^?1, respectively. The mineralization of ETU in the absence of hydrogen peroxide has led to the conclusion that ETU transformation products are susceptible to photolysis by UV light. These are promising results for further research. The processes that were investigated can be used to remove pesticide metabolites from drinking water sources and wastewater in developing countries.     

The persistence of insecticidal chemicals in soils treated with granular formulations of disulfoton and their uptake by potato plants

Abstract

Potatoes were grown from cut seed in Plainfield sand treated in‐furrow with disulfoton (Di‐Syston 15G, 3.36 kg Al/ha) in 1983 and from whole seed in similarly treated loam in 1991. Soils were contained in 2 m² field plots. Soil, seed potato and foliage were analyzed for the insecticide and its sulfoxide and sulfone metabolites during the 8–12 wk following planting. Disulfoton disappeared at different rates from the two soils (k_sand=0.024 day^‐1, k_loam=0.056 day^‐1) with partial conversion to the sulfoxide and sulfone in both. Larger quantities of the three insecticidal components were absorbed by the seed potato in the cut‐seed/sand combination. The relative amounts of these components in the seed potato also differed between treatments with disulfoton being the largest component of the cut‐seed/sand and smallest in the whole‐seed/loam. Disulfoton sulfoxide and sulfone were the major insecticidal components of the foliage and concentrations in the initial foliage (each ca. 10 ppm) were similar for both treatments. Sulfoxide concentrations in the foliage decreased more rapidly than the sulfone and the decrease in concentration of each of the components was similar for the two treatments.     

Biodegradation of Trifluralin in Harran Soil

Abstract

Degradation of trifluralin (α,α,α-trifluoro-2,6-dinitro-N,N-dipropyl-p-toluidine) was investigated in soils taken from three different locations at Harran region of Turkey under laboratory conditions. Surface (0–10 cm) soils, which were taken from a pesticide untreated field Gürgelen, Harran-1 and Ikizce regions in the Harran Plain, were incubated in biometer flasks for 350 days at 25°C. Ring-UL-¹⁴C-trifluralin was applied at the rate of 2 µg g^?1 with 78.7 kBq radioactivity per 100 g soil flask. Evolved ¹⁴CO₂ was monitored in KOH traps throughout the experiment. Periodically, soil sub-samples were removed and extracted by supercritical fluid extraction (SFE). Unextractable soil-bound ¹⁴C residues were determined by combustion. During the 350 days incubation period 6.6, 5.4, and 3.3% of the applied radiocarbon was evolved as ¹⁴CO₂ from the Harran-1, Gürgelen, and Ikizce soil, respectively. At the end of 350 days the SFE-extractable and bound ¹⁴C-trifluralin residues were 39.0 and 29.2% of the initially applied herbicide in Gürgelen soil. The corresponding values for Harran-1 and Ikizce soils were 36.2, 28.4% and 41.6, 18.5% respectively.     

Carbofuran degradation in soil profiles

Abstract

Two soils, Puyallup fine sandy loam from Puyallup, WA, and Ellzey fine sand from Hastings, FL, each with a prior history of carbofiiran exposure but with different pedological and climatological characteristics, were found to exhibit enhanced degradation toward carbofiiran in surface and subsurface soil layers. The treated Puyallup and Ellzey soils exhibited higher mineralization rates for both the carbonyl and the aromatic ring of carbofiiran when compared to untreated soils. Disappearance rates of [¹⁴C‐URL (uniformly ring labeled)] carbofiiran in the treated Ellzey soil was faster than in untreated soil, and also faster in surface soil than in subsurface soil. Initial degradation patterns in the treated Ellzey soil were also different from those in the untreated soil. The treated Ellzey soil degraded carbofuran mainly through biological hydrolysis, while untreated soil degraded carbofuran through both oxidative and hydrolytic processes.     

2株油烟降解优势菌株的筛选及性能研究

通过以油烟冷凝液为惟一碳源的选择培养基初筛,从长期受到油烟严重污染的土壤中筛选出具有降解油烟污染物能力的优势菌株XJ01、XJ03。研究了其最佳生长条件及降解性能,并对其进行了生理生化特征及分子生物学鉴定。研究表明,XJ01、XJ03最佳生长温度分别为35℃、30℃,最佳生长pH均为7,摇床转速均为120r／min,最佳降解时间分别为48h和36h;在最佳降解条件下,xJ01、XJ03总降解量分别达4．47113g／L和4．18ing／L,降解过程中,降解液pH值持续下降,生物量先增加后下降。经分子生物学鉴定,菌株XJ01、XJ03分别与铜绿假单胞菌群（Pseudomonasaeruginosagroup）和克雷伯氏菌属（Klebsiellasp．）同源性最高均达到100％。     

Atrazine degradation in a containerized rhizosphere system

Abstract

The effect of atrazine (2‐chloro‐4‐ethylamino‐6‐isopropylamino‐s‐triazine) on rhizosphere microorganisms and its fate in a containerized rhizosphere system was studied. The rhizosphere system consisted of corn grown in pot containing a defined potting mix of sand and bark with atrazine. Sterilized potting mix and a container without plants served as controls. Atrazine was extracted and analyzed via HPLC. Fluorescent pseudomonad populations increased 100‐fold in the rhizposphere during a 60‐day incubation period as compared to the nonvegetated control. Atrazine degradation was higher in the rhizosphere system (half‐life of 7 days) compared to the nonvegetated control (half‐life of greater than 45 days). The major degradation product detected in the rhizosphere system was deisopropylatrazine; other products detected included deethylatrazine, deethylhydroxyatrazine, deisopropylatrazine and hydroxyatrazine. Hydroxyatrazine was detected in the nonvegetated and sterile controls. The containerized rhizosphere system provides an experimental system to study the fate of pesticidal chemicals as well as the effects on microbial populations.     

Degradation behaviour of pyrazosulfuron-ethyl in water as affected by pH

Pyrazosulfuron-ethyl, a new herbicide belonging to the sulfonylurea group, is used for weed control in rice crops growing in areas varying from acidic to alkaline soils. This study was undertaken to determine the degradation behaviour of pyrazosulfuron-ethyl in distilled water and buffer solutions at pH 4, 7 and 9. Degradation was pH-dependent and herbicide was least persistent in acidic pH followed by alkaline and neutral pH. The half-life of pyrazosulfuron-ethyl varied from 2.6 days (pH 4) to 19.4 days (pH 7) and half-life in distilled water was comparable to half-life at pH 7 buffer. HPLC analysis of different pH samples showed the formation of three metabolites viz., 5-(aminosulfonyl)-1-methyl-1H-pyrazole-4-carboxylic acid; ethyl 5-(aminosulfonyl)-1-methyl-1H-pyrazole-4-carboxylate and 2-amino-4,6-dimethoxy pyrimidine. The formation of pyrazosulfuron acid [5-([([(4,6-dimethoxy-2 pyrimidinyl)-amino]-carbonyl) amino]-sulfonyl)-1-methyl-1H-pyrazole-4-carboxylic acid] was not observed at any pH. The study indicated that the herbicide was least stable under acidic conditions and the predominant degradation route of pyrazosulfuron-ethyl in water is hydrolysis of sulfonamide linkage.     

高效石油烃降解菌SKD-1的分离、筛选及其降解性能

从孤岛油田石油污染土壤中分离到一株高效石油降解菌,命名为SKD-1。该菌株菌落表面湿润光滑、边缘整齐、圆形、不透明、乳黄色,能够利用葡萄糖和淀粉作为其生长的碳源和能源,其最适生长环境为碱性（pH8-10）,在分别以正十六烷烃和原油为惟一碳源,温度为30℃,摇床（180r／min）培养的条件下,菌株SKD-1的降解率分别为66．1％和36．9％。16SrRNA基因序列分析表明,菌株SKD-1与不动杆菌AcinetobactercalcoaceticusSY-1同源性达99％。结合菌株SKD．1菌落形态、理化性质以及系统发育分析,可以鉴定菌株SKD-1属于不动杆菌属（Acinetobactersp．）,序列登录号为AB774229。