Carbon source/sink function of a subtropical, eutrophic lake determined from an overall mass balance and a gas exchange and carbon burial balance

Although studies on carbon burial in lake sediments have shown that lakes are disproportionately important carbon sinks, many studies on gaseous carbon exchange across the water-air interface have demonstrated that lakes are supersaturated with CO(2) and CH(4) causing a net release of CO(2) and CH(4) to the atmosphere. In order to more accurately estimate the net carbon source/sink function of lake ecosystems, a more comprehensive carbon budget is needed, especially for gaseous carbon exchange across the water-air interface. Using two methods, overall mass balance and gas exchange and carbon burial balance, we assessed the carbon source/sink function of Lake Donghu, a subtropical, eutrophic lake, from April 2003 to March 2004. With the overall mass balance calculations, total carbon input was 14 905 t, total carbon output was 4950 t, and net carbon budget was +9955 t, suggesting that Lake Donghu was a great carbon sink. For the gas exchange and carbon burial balance, gaseous carbon (CO(2) and CH(4)) emission across the water-air interface totaled 752 t while carbon burial in the lake sediment was 9477 t. The ratio of carbon emission into the atmosphere to carbon burial into the sediment was only 0.08. This low ratio indicates that Lake Donghu is a great carbon sink. Results showed good agreement between the two methods with both showing Lake Donghu to be a great carbon sink. This results from the high primary production of Lake Donghu, substantive allochthonous carbon inputs and intensive anthropogenic activity. Gaseous carbon emission accounted for about 15% of the total carbon output, indicating that the total output would be underestimated without including gaseous carbon exchange.     

Spatial distribution of organochlorine pesticides (OCPs) and effect of soil characters: A case study of a pesticide producing factory

The distribution and concentration of some organochlorine pesticides (OCPs) in the soil around a pesticide factory in Zibo, China, were examined, including dichlorodiphenyltrichloroethane (DDT) and its metabolites, isomers of hexachlorocyclohexane (HCH) and endosulfan (ENDO). The results showed that the OCPs concentrations were extraordinary high in this region. The concentrations of DDTs, HCHs, and ENDO were measured in the range of 0.775–226.711, 0.248–42.838, and 0.081–1.644 mg kg^?1, respectively. DDT and its isomers were identified to be the dominate contaminants in most of the sampling sites. In the vertical direction, the distribution pattern of the total OCPs was in order of DDTs, HCHs, and ENDO in the 0–20 cm, but in 20–40 and 40–60 cm the trends were unobvious. Although no recent input occurred in most areas, the residues of OCPs remained in deep soil due to their persistence. Unlike ENDO, DDTs and HCHs appeared to have the similar property in terms of not only the migration pattern in soil, but also the relationship to the same dominant impact factor (i.e. organic matter). DDTs and HCHs were affected positively by the organic matter, whereas ENDO was affected negatively. Due to the interrelationship among various impact factors, the spatial distribution of pesticides in the soil was considered to be a combined result.     

皮革废水混凝处理实验研究

采用混凝剂对皮革废水进行混凝处理。对3种无机混凝剂和一种有机混凝剂进行了筛选,研究了pH值和投药量对废水中SS、COD、铬和色度等污染物去除效果的影响。结果表明,当pH值在酸性和中性时,效果不明显;当pH值为碱性时,效果显著。硫酸亚铁、硫酸亚铁+PAM和聚合氯化铝(PAC)+PAM 3种混凝剂组合具有良好的混凝效果,在合适的pH值和投药量下,SS和COD的去除率分别达到80%和30%以上,铬和色度的去除率分别达到95%和50%以上。且硫酸亚铁混凝效果好,成本低,适合小型皮革企业需求。     

自养反硝化技术研究进展

介绍了近年来水体硝酸盐污染的原因及危害,阐述了反硝化技术的特点及主要原理,综述了以硫及氢为电子供体的自养反硝化技术的发展及运用,探讨了其今后的研究方向和前景。     

人类特异性粪厌氧菌基因标记物实时荧光定量PCR检测方法的建立和应用

针对人类粪便污染,选择来源于拟杆菌和双歧杆菌16S rRNA的基因片段作为标记物,分别建立了相应的实时荧光定量PCR检测方法.选取不同来源的粪便样品进行检测,证实了引物的特异性.回收纯化从污水中扩增所得的目标PCR片段,经过连接转化,筛选阳性克隆提取其重组质粒作为实时荧光定量PCR的标准品.通过检测一系列梯度稀释的标准品,确定了拟杆菌基因标记物和双歧杆菌基因标记物定量PCR检测方法分别在1.98×102～1.98×107 copy/μL和2.12×101～2.12×107 copy/μL范围内具有良好的线性关系.     

Disinfection by-product formation potentials in wastewater effluents and their reductions in a wastewater treatment plant

Disinfection by-product formation potentials (DBPFPs) in wastewater effluents from eight wastewater treatment plants (WWTPs) were investigated. In addition, a WWTP with one primary effluent and two different biological treatment processes was selected for a comparative study. Formation potential tests were carried out to determine the levels of DBP precursors in wastewater. WWTPs that achieved better organic matter removal and nitrification tended to result in lower DBPFPs in effluents. For the WWTP with two processes, haloacetic acid, trihalomethane, and chloral hydrate precursors were predominant DBP precursors in the primary and secondary effluents. The percent reductions of haloacetonitrile and haloketone formation potentials averaged at 96% which was high in comparison to the reductions of other classes of DBPFPs. In addition, biological treatment changed the DBPFP speciation profile by lowering the HAAFP/THMFP ratio. The eight plant survey and the comparative analysis of the WWTP with two processes implied that besides nitrification, there may be other confounding factors impacting DBPFPs. Oxic and anoxic conditions, formation and degradation of soluble microbial products had impacts on the DBPFP reductions. This information can be used by water and wastewater professionals to better control wastewater-derived DBPs in downstream potable water supplies.     

二氧化钛颗粒制备及其对水中三价砷的去除

以硫酸氧钛和聚乙烯醇(PVA)为原料,通过冰水浴法制备了二氧化钛(TiO2)颗粒,并研究了其对砷的吸附性能。利用X射线衍射仪(XRD)和扫描电子显微镜(SEM)对TiO2颗粒进行了表征,结果表明,吸附剂为锐钛矿结构,比表面积246 m2/g。TiO2颗粒对模拟地下水中砷(Ⅲ)的吸附动力学研究表明,吸附过程符合准二级动力学。采用Langmuir和Freundlich方程对吸附平衡数据进行了拟合,结果表明,吸附等温线符合Langmuir模型,最大吸附量为22.3 mg/g。TiO2颗粒对三价砷的吸附在pH为9.1时吸附量最大,吸附受CO23-影响较大。将110 g TiO2颗粒装备成过滤滤壶,对山西地下水(总砷含量190μg/L)进行了除砷实验,经过3 600柱体积后,滤液中砷浓度低于10μg/L,符合国家饮用水标准。     

环境测试舱自吸附甲醛重释放规律与影响因素研究

广泛用于板材污染物释放量测试、空气净化产品净化效果测试等实验中的环境测试舱,往往由于其内壁黏附性杂质而对目标测试物产生不可忽视的自吸附作用,自吸附污染物将作为二次释放源出现重释放,研究目标测试物的自吸附消耗量及重释放规律,探索有效控制措施,有利于对环境测试舱实验应用及室内污染控制提出指导性实际意义。分别选取0.2%甲醛溶液、大芯板作为同一自制玻璃环境测试舱2期实验(I期、Ⅱ期)的不同甲醛释放源,通过近90 d追踪测试,经不同释放源、不同控制条件下舱内壁自吸附甲醛的多次重释放实验,结合非线性拟合分析方法,总结出舱内壁自吸附甲醛重释放甲醛浓度变化符合一阶递增指数函数:y=A1×exp(-x/t1)+y0,(A1<0、t1>0)。曲线参数y0值可用于评价实验条件下测试舱内自吸附甲醛残余量;y0值与环境舱舱体材质、环境温湿度、舱外甲醛浓度及空气交换手段有关,而与释放源及其释放平衡浓度高低无明显关系。大开舱门短时间抽气式空气交换对舱内自吸附甲醛残余有适度清除效果,使y0值降低,同时有利于再次平衡状态的快速建立;而长时间的无动力空气交换,或者自来水洗及去离子水洗等处理手段对舱内壁自吸附甲醛残余无明显清除作用。     

腐殖酸和铁对阿特拉津光降解影响的研究

为考察除草剂在水体中的自净性能，对模拟太阳光(λ> 290 nm)下腐殖酸和铁元素对阿特拉津的光化学降解进行了研究。结果表明，单独辐照阿特拉津几乎不降解。在分别加入3、5和10 mg/L的腐殖酸时，阿特拉津的降解率分别为34.36 %、40.74%和15.66 %；在Fe(Ⅲ)投加量从0.01 mmol/L增加到0.2 mmol/L时，阿特拉津的降解率从24.36 %增加到34.97 %。而在当腐殖酸与铁共存时，阿特拉津降解率则进一步提高。紫外可见光谱和荧光光谱均表明，腐殖酸-铁络合物的形成及其光化学作用，促进了阿特拉津的降解。     

生活垃圾焚烧发电厂烟尘中重金属沉降对土壤环境影响分析

本文以一日处理生活垃圾2250t的生活垃圾焚烧发电厂为例,根据其重金属的排放量,预测重金属随大气扩散、迁移,最终通过自然降水和自然沉降进入土壤后,对土壤环境的影响。结果表明,项目建成后的20年内,大气评价范围内土壤中重金属的累计值满足《土壤环境质量建设用地土壤污染风险管控标准(试行)》 (GB36600-2018)表1中第二类用地筛选值要求。