不同土地利用方式对土壤有机碳及其组分影响研究

测定了5种土地利用方式下（人工草地、围封样地、一年耕地、弃耕地、自由放牧样地）土壤有机碳、土壤微生物生物量碳、易氧化态碳和轻组有机碳组分含量特征,比较分析土地利用变化对典型草原土壤起源下土壤有机碳组分的变化。结果表明,1）人工草地土壤有机碳含量为（14．98±3．47）g·kg-1,围封样地的为（12．41±6．40）g·kg-1,一年耕地的为（12．20±5．59）g·kg-1,弃耕样地的为（10．39±5．08）g·kg-1,自由放牧样地的为（9．45±3．19）g·kg-1。人工草地土壤有机碳含量明显高于其他样地,围封样地和一年耕地的含量相似,自由放牧样地的含量最小。2）土壤微生物生物量碳、易氧化态碳和轻组有机碳的含量在不同土地利用方式下的变化趋势与土壤有机碳含量的变化趋势基本一致。土壤有机碳及其组分含量在土壤剖面上,随着土层深度的增加而逐渐降低。3）土壤微生物生物量碳、易氧化态碳和轻组有机碳的平均分配比率在不同类型样地范围分别为0．24％～0．66％、0．002％～0．019％和0．05％-0．25％,显示出各组分对土壤环境变化的敏感度不同,其中土壤微生物生物量碳更能反映土壤有机碳的早期变化,可以作为表征土壤有机碳变化和土壤肥力的敏感指标。     

亲水性多孔载体在流化床中的生物膜形成过程分析

采用实验制备的一种新型亲水性多孔聚合物作为流化床反应器中生物膜附着生长的载体,实现流态化水力条件下的生物挂膜过程.在3个结构尺寸相同的流化床反应器中考察了接种污泥浓度、进水有机负荷及载体粒径对亲水性多孔载体生物挂膜量的影响,试验结果表明,接种污泥浓度为30 g VSS/L、进水TOC值为350 mg/L、载体粒径为5～8 mm时载体表面的附着生物量最大,反应器运行12 d的载体附着生物量达到4.45 g VSS/L,膜结构稳定,表现出较活性污泥法更高的活性.在进水TOC、氨氮浓度分别为350 ms/L、50 mg/L,HRT为6 h的情况下,两者的去除率分别达到了97.1%和64.3%,表明载体上的生物膜对污水中TOC及氨氮的去除表现出高效率.挂膜后载体表面上的微生物以丝状菌为主,孔壁上的微生物以球菌和杆菌为主要生物相,证明载体内外表面皆适宜微生物的生长,并且形成合理的生物相分布.     

铁炭内电解-厌氧-好氧工艺处理阿维菌素废水的试验研究

血清瓶毒性试验表明 ,AVM对厌氧消化产生强烈的抑制作用。AVM废水经铁炭内电解预处理后 ,COD和AVM的去除率分别达到 19.5 %和 6 8.5 % ,可大大降低废水的毒性。预处理出水再经UASB +生物接触氧化反应器进一步处理 ,当生化系统进水COD为 6 0 0 0— 6 5 0 0mg/L时 ,出水COD为 2 5 0— 2 80mg/L ,总COD去除率达到 95 .6 % ,出水达到生物制药行业排放标准     

Rapid degradation of butachlor in wheat rhizosphere soil

The degradative characteristics of butachlor in non-rhizosphere, wheat rhizosphere, and inoculated rhizosphere soils were measured. The rate constants for the degradation of butachlor in non-rhizosphere, rhizosphere, and inoculated rhizosphere soils were measured to be 0.0385, 0.0902, 0.1091 at 1 mg/kg, 0.0348, 0.0629, 0.2355 at 10 mg/kg, and 0.0299, 0.0386, 0.0642 at 100 mg/kg, respectively. The corresponding half-lives for butachlor in the soils were calculated to be 18.0, 7.7, 6.3 days at 1 mg/kg, 19.9, 11.0, 2.9 days at 10 mg/kg, and 23.2, 18.0, 10.8 days at 100 mg/kg, respectively. The experimental results show that the degradation of butachlor can be enhanced greatly in wheat rhizosphere, and especially in the rhizosphere inoculated with the bacterial community designated HD which is capable of degrading butachlor. It could be concluded that rhizosphere soil inoculated with microorganisms-degrading target herbicides is a useful pathway to achieve rapid degradation of the herbicides in soil.     

Distribution of alkylphenols in the Pearl River Delta and adjacent northern South China Sea, China

The occurrence of alkylphenols (APs) was investigated in surface water and sediments from the Pearl River Delta and adjacent northern South China Sea. Most of the water samples contained detectable amounts of APs, ranging up to 0.628 microg l(-1) for nonylphenol (NP) and 0.068 microg l(-1) for octylphenol (OP). APs were found in all of the sediment samples with concentrations ranging from 59 to 7808 microg kg(-1) for NP and from 1 to 93 microg kg(-1) for OP. The Zhujiang River showed the highest concentrations of APs in both water and sediments. Significant decrease of APs concentrations going from the Zhujiang River to the Shiziyang River was observed. The Xijiang River contained concentrations of APs slightly higher in water but relatively lower in sediments than the Lingding Bay, which might be attributed to their different hydrodynamic and sedimentary characteristics. There was a decreasing trend of APs in water from the rivers to the estuary and further to the sea on the whole. In the Lingding Bay and its outer waters, concentrations of APs in sediments increased to a maximum and then decrease seaward, which was consistent with the distribution trend of the sediment organic carbon contents. Linear regression analyses showed the concentrations of APs were markedly correlated with the sediment organic carbon contents, indicating that the sediment organic carbon is an important factor controlling the levels of APs in sediments.     

介质阻挡放电对湖泊水华蓝藻的去除

采用介质阻挡放电等离子体技术去除太湖水华蓝藻,考察了放电输出功率、空气流速、添加剂(异丙醇、腐植酸)等对蓝藻去除的影响。结果表明,介质阻挡放电能去除太湖水华蓝藻,放电功率100 W,空气流速1.0 L/min,放电18min,在光照强度2 000 lx和25℃下培养4 d,初始叶绿素a浓度为9.58 mg/L藻液中蓝藻去除率达87.8%。增加放电输出功率和空气流速能提高蓝藻的去除效率;腐植酸促进了介质阻挡放电对蓝藻的去除;而异丙醇添加剂抑制了介质阻挡放电的作用。放电处理后,蓝藻细胞内类胡萝卜素含量、SOD活性、MDA含量发生明显变化,介质阻挡放电破坏了蓝藻细胞内含物。     

Genotoxicity of two novel pesticides for the earthworm, Eisenia fetida

In this paper, several studies were conducted to evaluate the genotoxicity of two pesticides, Imidacloprid and RH-5849, for earthworm (Eisenia fetida). Earthworms were exposed in different exposure systems to evaluate their acute toxicity and the genotoxicity of the two pesticides was evaluated by using the method of sperm deformity assessment, micronucleus test of root tip cells in Vicia faba, a mouse bone-marrow micronucleus test, and comet assay. LC(50) (interpolated concentration at which 50% mortality of test population occurs) for earthworms varied in different exposure systems. The results indicated that Imidacloprid was consistently more toxic than RH-5849 in all exposure systems. In this study, sperm deformity test was used to detect the potential adverse influences of pesticides on the reproduction of earthworms. The results demonstrated that significant induction of sperm deformity (p<0.01) and a dose-effect relationship displayed at Imidacloprid concentrations higher than 0.5 mg/kg dry soil. However, the sperm deformity frequency of groups exposed to RH-5849 did not show significant difference (p>0.05) from the control until the dose reached 100 mg/kg dry soil. The results of the V. faba micronucleus tests showed that micronuclei frequency of the exposed group did not show significant difference (p>0.05) from the control until the concentration of Imidacloprid and RH-5849 reached 100 mg/ml. The results of the mouse bone-marrow micronuclei test also indicate that two pesticides did not show significant effects (p>0.05) on the micronuclei frequency in mice bone-marrow cells until the dose reached 100 mg/kg for Imidacloprid and 300 mg/kg for RH-5849 (2/3 LD(50)). Although no genotoxicity was detected by using the micronucleus tests, the results of the comet assay showed that the two pesticides induce significant DNA damage (p<0.01) in earthworms and dose-effect relationships were displayed. The 'earthworm comet assay' is a rapid and sensitive way to screen chemicals or terrestrial environments for their DNA-damaging properties.     

Photocatalytic oxidation of triclosan

In the spring of 2003, there was an outbreak of the severe respiratory syndrome (SARS) in Hong Kong. Health concerns have thus triggered an increased and predominant use of various types of household cleansing agents such as triclosan (5-chloro-2-(2,4-dichlorophenoxy)phenol). However, it has been reported recently that triclosan could be photochemically converted to toxic 2,8-dichlorodibenzo-p-dioxin (2,8-Cl(2)DD) in the environment. It is therefore necessary to develop environmentally friendly methods for the treatment of triclosan. To this end, photocatalytic degradation of triclosan in aqueous solution was conducted using TiO(2) (Degussa P25) under irradiation of UV light (lambda < 365 nm). It was found that triclosan could be degraded by this approach. Hydrogen peroxide was added to enhance the degradation process, and the optimal initial hydrogen peroxide concentration for triclosan degradation was 0.005% (w/v). Product identification indicated that triclosan oxidation occurred at its phenol moiety and yielded quinone and hydroquinone intermediates. The formation of a dichlorophenol intermediate in triclosan degradation suggested bond-breaking of the ether linkage occurred during the process. Moreover, no chlorinated dibenzo-p-dioxin congener was detected. These findings confirm that the photocatalytic degradation of triclosan is an environmentally friendly process.     

Effects of EDTA and low molecular weight organic acids on soil solution properties of a heavy metal polluted soil

A pot experiment was conducted to study the effects of EDTA and low molecular weight organic acids (LMWOA) on the pH, total organic carbon (TOC) and heavy metals in the soil solution in the rhizosphere of Brassica juncea grown in a paddy soil contaminated with Cu, Zn, Pb and Cd. The results show that EDTA and LMWOA have no effect on the soil solution pH. EDTA addition significantly increased the TOC concentrations in the soil solution. The TOC concentrations in treatments with EDTA were significantly higher than those in treatments with LMWOA. Adding 3 mmol kg(-1) EDTA to the soil markedly increased the total concentrations of Cu, Zn, Pb and Cd in the soil solution. Compared to EDTA, LMWOA had a very small effect on the metal concentrations. Total concentrations in the soil solution followed the sequence: EDTA > citric acid (CA) approximately oxalic acid (OA) approximately malic acid (MA) for Cu and Pb; EDTA > MA > CA approximately OA for Zn; and EDTA > MA > CA > OA for Cd. The labile concentrations of Cu, Zn, Pb and Cd showed similar trends to the total concentrations.     

混合酶强化剩余污泥微生物燃料电池性能

为了提高剩余污泥为燃料的微生物燃料电池(SMFC)产电性能以及污泥减量化效果,在不同的温度(40、45和50℃)研究单室无膜微生物燃料电池中酶对SMFC产电特性的强化效果.加入单一酶(蛋白酶或α-淀粉酶)的结果表明,随着温度的上升,SMFC功率密度均上升,但40℃时强化效果最明显,与加入失活酶的对照组相比分别增加198％和130％.在40℃下,混合酶比(蛋白酶浓度:淀粉酶浓度)为2∶3时,SMFC最大功率密度为776 mW/m2.随着混合酶中淀粉酶的比例提高,SMFC库伦效率逐渐增加,当混合酶比为4∶1时,CE(库伦效率)可达18.3％,同时TCOD、TSS和VSS去除率分别为70.3％、66.7％和80.4％.因此,温度相对较低时,外加酶强化效果更明显;与单种酶相比,混合酶对SMFC产电性能和污泥减量化的强化效果更显著.