久效磷对秀丽隐杆线虫运动、学习和觅食行为的影响

久效磷(MCP)是一种广谱类内吸附性有机磷农药和潜在的神经毒剂,能够对非靶生物产生神经毒性作用,而行为毒性是神经毒性的主要表现形式. 以运动、学习与觅食行为、乙酰胆碱酯酶活性为指标,研究了久效磷对非靶生物——秀丽隐杆线虫(Caenorhabditis elegans,下称线虫)行为的影响. 结果显示:经0.5、5.0和50.0 mg/L久效磷暴露后,各暴露组线虫头部摆动和身体弯曲频率均极显著降低,0.5 mg/L暴露组线虫向前摆动频率显著减少,5.0和50.0 mg/L暴露组线虫向前摆动频率极显著减少;5.0和50.0 mg/L暴露组线虫在NaCl存在和缺少食物条件下,对NaCl的趋向性极显著升高;与对照组相比,50.0 mg/L暴露组线虫菌落接触率在2、4、6、8 h时均显著降低,在24 h时极显著降低;各暴露组线虫的乙酰胆碱酯酶活性均受到极显著抑制. 表明久效磷能够导致线虫运动、学习与觅食行为的严重缺陷,乙酰胆碱酯酶活性抑制与久效磷对线虫运动行为的影响呈正相关,与其学习行为的影响呈负相关.      

基于新型载体AMC/UASB-SCMBBR生物工艺处理印染废水的中试研究

针对泉州某印染厂实际废水(COD 800～1800 mg·L~(-1),NH~+_4-N 20～50 mg·L~(-1),pH=8～14),以两种新型载体分别作为厌氧与好氧单元中微生物固定化载体,考察了中试规模上流式厌氧污泥床反应器(UASB)与柔性悬浮载体移动床生物膜反应器(SCMBBR)组合工艺对该废水的处理效果.4个月的连续试验结果表明:①经过30 d前期调试运行该工艺系统成功启动,处理量为1.5～2.2 m~3·d~(-1)时,AMC/UASB和SCMBBR反应器对COD的去除率分别达到22%和50%,AMC/UASB反应器出现明显的产气现象,SCMBBR中载体挂膜状况良好;②启动完成后经过90 d的连续运行,当AMC/UASB和SCMBBR反应器水力停留时间分别为10.7 h和8.8 h,废水处理量为5 m~3·d~(-1)时,稳定运行阶段整个工艺废水COD去除率达到78%,出水氨氮平均浓度为3.4 mg·L~(-1);此外,整体工艺色度去除率达到65%,其中,厌氧段色度去除率达到50%左右;③通过分析计算,整个系统污泥减量达到67.7%～76.6%,该生物组合工艺具有明显的污泥减量效果.     

生物炭对土壤中硫的迁移转化及植物有效性的影响研究

土壤中的硫是作物生长发育不可缺少的营养元素,也是合成植物体内蛋白质、核酸等的重要组成成分.硫素是不可再生资源,充分合理的利用现有的硫素资源,对于保持硫素的循环平衡具有重要意义.生物炭一般指农林废弃物在厌氧或缺氧条件下高温热解生成的一种富碳颗粒,因其在土壤性质改良等方面的广泛应用而备受关注.生物炭施入土壤,将直接或间接影响土壤中硫的植物有效性.评述了生物炭对土壤中硫素有效性的重要研究进展,为生物炭的农业应用提供参考价值.     

Effect of Ni–V loading on the performance of hollow anatase TiO2 in the catalytic combustion of dichloromethane

A catalyst based on mixed V-Ni oxides supported on TiO_2(Ni-V/TiO_2)was obtained using the sol-gel method.Its catalytic performance relative to dichloromethane(DCM)degradation was investigated.Characterization and analysis were conducted using transmission electron microscopy,H2 temperature-programmed reduction,pyridine-Fourier transform infrared spectroscopy(FTIR)characterization,and X-ray diffraction.Results showed that the original hollow anatase structure of pure Ti02 was well-maintained after Ni-V loading.The loading of NiO-VOx not only significantly improved the stability of pure Ti02 but also inhibited the formation of the by-product monochloromethane(MCM).Among the series of Ni-V/TiO_2 catalysts,4%Ni-V/TiO_2 possessed the highest catalytic activity,with 90%DCM conversion at only 203℃.No by-products and no significant changes in the catalytic activity were observed during combustion of DCM after 100 hr of a continuous stability test.Furthermore,thermogravimetric analysis(O_2-TG)and energy dispersive spectrometer(EDS)characterization of the used 4%Ni-V/TiO_2 catalyst revealed that no coke deposition or chlorine species could be detected on the catalyst surface.     

苏州河生态恢复初期自净能力的综合评估方法

利用苏州河水的化学及生物学参数,以及水样对几种添加化学品的降解延滞期及降解率,综合评估了水体自净能力,并探讨了苏州河生态恢复初期自净能力的评估方法。对比2008年上、下游水样对醋酸钠、苯酚、苯胺、二甘醇、乙二醇、三聚乙醛等6种化学品的降解情况,比较分析了2006年及2008年两年度间苏州河自净能力的变化。相对2006年而言,2008年水体的氧化还原电位急剧下降,上、下游水体对化学品降解能力整体减弱,三聚乙醛降解能力的减弱尤为明显,降解率从2006年的77.82%和88.73%降至2008年的35.83%和65.86%。在外部有机物输入量无明显变化的情况下,上游的好氧异养菌数由2006年的4.7×104CFU/mL降为2008年的2.2×103CFU/mL。2008年苏州河上游水体对化学品(二甘醇除外)降解能力较下游水体更弱,且延滞期长。与2006年相比,2008年苏州河水体的自净能力整体减弱,上游水体自净能力的损失更为明显。     

Chemical characterization of size-resolved aerosols in four seasons and hazy days in the megacity Beijing of China

Size-resolved aerosol samples were collected by MOUDI in four seasons in 2007 in Beijing. The PM₁₀ and PM_1.8 mass concentrations were 166.0 ± 120.5 and 91.6 ± 69.7 μg/m³, respectively, throughout the measurement, with seasonal variation: nearly two times higher in autumn than in summer and spring. Serious fine particle pollution occurred in winter with the PM_1.8/PM₁₀ ratio of 0.63, which was higher than other seasons. The size distribution of PM showed obvious seasonal and diurnal variation, with a smaller fine mode peak in spring and in the daytime. OM (organic matter = 1.6 × OC (organic carbon)) and SIA (secondary inorganic aerosol) were major components of fine particles, while OM, SIA and Ca^2 + were major components in coarse particles. Moreover, secondary components, mainly SOA (secondary organic aerosol) and SIA, accounted for 46%–96% of each size bin in fine particles, which meant that secondary pollution existed all year. Sulfates and nitrates, primarily in the form of (NH₄)₂SO₄, NH₄NO₃, CaSO₄, Na₂SO₄ and K₂SO₄, calculated by the model ISORROPIA II, were major components of the solid phase in fine particles. The PM concentration and size distribution were similar in the four seasons on non-haze days, while large differences occurred on haze days, which indicated seasonal variation of PM concentration and size distribution were dominated by haze days. The SIA concentrations and fractions of nearly all size bins were higher on haze days than on non-haze days, which was attributed to heterogeneous aqueous reactions on haze days in the four seasons.     

Carbon and nitrogen composition and stable isotope as potential indicators of source and fate of organic matter in the salt marsh of the Changjiang Estuary, China

Elemental (TOC, TN, C/N) and stable carbon and nitrogen isotopic (delta(13)C, delta(15)N) compositions were measured for surface sediments, three sediment vibrocores, plants, and suspended particulate matter (SPM) collected from salt marsh of the Changjiang Estuary. The purpose of this study is to characterize the sources of organic matter in sediments and to further elucidate the factors influencing the isotope signature in the salt marsh. Our results indicate that organic matter preserved in the sediments is predominantly controlled by the particulate organic matter in the Changjiang Estuary. The in situ contribution of marsh plants carbon to sediment organic matter is clearest in the high marsh, where the low delta(13)C of the plants (-28.1 per thousand) is reflected by a sediment delta(13)C (-24.7 per thousand) lower than values found for the low marsh and bare flat sediments (-23.4 per thousand and -23.0 per thousand, respectively). The effect of grain size on the spatial difference of isotope composition in the marsh sediments is insignificant, based on the observation that similar isotope values are found in different size particles, both for delta(13)C and delta(15)N. Nutrient utilization by plant assimilation, however, shows great impact on the surface sediment delta(15)N composition, due to the isotope fractionation. With extensive plant coverage and the consequent low surface water nitrate concentration, delta(15)N values of the high marsh surface sediments show (15)N enrichment.     

A sensitive and reliable quantification method for Bisphenol A based on modified competitive ELISA method

Bisphenol A (BPA), generally known as bisphenols, has been identified as a potential estrogenic substance. BPA must be conjugated to carrier protein and BSA was commonly used. 4,4-Bis(4-hydroxyphenyl) valeric acid (BHPVA) has a bisphenolic structure and a long carbon chain with a reactive carboxyl group on the end. In this study, BHPVA-BSA was used to produce polyclonal antibody against bisphenolic structure, and a modified competitive ELISA method for quantification of BPA was developed. This system was based on BHPVA-BSA for polyclonal antibody production against bisphenolic structure, and BHPVA-HRP for determination of BPA substituting detection antibody in competitive reaction. Recovery was assessed at 10 different concentrations (2-1000 ng/ml) of BHPVA, and the recovery range was from 96.3% to 107.2%. The variation was from 6.2% to 9.8% for intra assay and from 10.1% to 12.6% for inter assay. The quadratic was used to establish the curve regression. The range was found to be between 2 and 1000 ng/ml. This modified competitive ELISA method has proven to be a very useful tool for quantification of BPA without the unexpected interaction of BSA and anti-BSA polyclonal antibody.     

pH对氢自养型反硝化菌反硝化性能的影响

采用模拟硝酸盐污染地下水(简称模拟水)驯化培养氢自养型反硝化菌,建立了定量分析氢自养型反硝化菌生物量的方法,研究了pH对氢自养型反硝化菌反硝化性能的影响。结果表明,每单位OD600相当于水样中氢自养型反硝化菌的生物量为491.75mg/L。当初始pH在6.7以下或9.2以上时,氢自养型反硝化菌生物活性会受到抑制,而初始pH为7.2、7.7、8.2和8.7时,反硝化进行12h后模拟水中的总氮去除率分别为99.7%、99.6%、96.6%和83.5%。经过12h的反硝化模拟水的pH增加0.1～0.9,硬度降低10.01～48.05mg/L;初始pH为6.7～8.7的模拟水在反硝化进行12h后生物量增加5.68～6.03mg/L,初始pH为7.7的模拟水反硝化速率最高,达0.041mg/h。     

Ag~+-TiO_2/AC复合材料的可见光吸附-光催化协同作用

采用水热法制备活性炭负载银掺杂纳米Ti O2复合材料(Ag+-Ti O2/AC),对样品进行了TEM、XRD、FT-IR和UV-Vis表征,分析了Ag+-Ti O2/AC的微结构、吸收谱特性和掺杂银离子后的半导体带隙变化,并研究了其在可见光下对甲基橙溶液(MO)的降解性能。结果表明,水热法不需要高温处理即可得到高活性的锐钛矿相纳米Ti O2,Ag+掺杂和AC负载均明显提高Ti O2光催化剂的光催化活性,在可见光下光照180 min,0.2 g/L的Ag+-Ti O2/AC对10 mg/L的甲基橙溶液的降解率为73.7%,主要由于存在持续的活性炭局域强吸附-Ti O2光催化降解协同作用,明显提高了甲基橙的降解效率。