物种多样性对植物生长与土壤镉污染修复的影响

土壤重金属污染是当今最为突出的环境问题之一,其中,重金属镉(Cd)已成为我国受污染土壤中最主要的无机污染物之一.植物修复法是去除土壤重金属的重要方法,研究表明,植物物种多样性的增加能促进生态系统功能.那么在Cd污染土壤中,植物物种多样性对植物生长和Cd污染修复会有怎样的影响,其内在机理是怎样的并不清楚.基于此,本研究选择6种本地常见草本植物(荆芥、鸡眼草、短叶水蜈蚣、牛筋草、鸭跖草和细风轮菜),通过室内控制实验研究不同植物物种多样性(1-,2-,3-,6-物种)对植物生长与土壤Cd污染修复的影响.结果表明:植物物种多样性的增加显著促进植物地下生物量和总生物量的积累,并对植物根系形态(根总长、根总表面积、根尖总数与根平均直径)和叶绿素荧光参数(PSII最大光能转化效率F_v/F_m和PSII潜在活性F_v/F_0)有显著的促进作用;植物物种多样性的增加能显著提高植物地上、地下及总Cd含量(积累量)和富集系数;植物物种多样性的增加对植物生长、根系形态指标及Cd的富集具有显著的净效应,且以互补效应为主.本研究选取的是对环境条件要求不高、生长周期短的本地草本植物,可为利用本地常见短世代周期植物进行土壤重金属污染修复提供理论依据.     

大港地区大气颗粒物中多环芳烃分布及污染源识别的研究

多环芳烃（PAHs）是一类对人体危害较大的有机污染物。目前对大气环境中PAHs来源识别技术还处于探索与发展阶段。为了解天津大港油田地区大气环境中PAHs污染状况与来源,对天津市大港地区大气颗粒物中10种PAHs分布及污染源开展了调查。结果表明：大港地区10种PAHs总浓度平均为169ng/m3,比市区对照点的465ng/m³低63.7％,其中苯并（a）芘（BaP）平均浓度为13.6ng/m³,比市区对照点的41.1ng/m³低66.9％。实验结果经统计处理发现BaP浓度与其它9种PAHs浓度存在一定的相关性,相关系数均在0.60以上。利用比值法进行源识别得出：大港石化区PAHs主要来源为燃煤污染;而大港油田区PAHs主要来源为燃油污染。     

废弃采石场作为一般工业固体废物填埋场址探析

从城市工业固体废物消纳和废弃采石场作为填埋处置场地的角度出发,对利用废弃采石场作为第Ⅰ类一般工业固体废物填埋场场址条件进行探讨,通过广州市地区实例说明利用废弃采石场选址作为第Ⅰ类一般工业固废填埋场址的可用性,这对未来废弃采石场的综合利用具有一定的借鉴意义。     

武汉东湖部分原生动物种类污染值的建立

利用对武汉东湖进行的为期１ 年的原生动物采集及鉴定结果以及同时进行的水质化学测试结果,对所建立的原生动物生物指数进行了验证,表明所得ＣＰＶ与化学综合污染指数呈显著的相关,说明建立的生物指数对淡水水系有广泛的实用性．对汉江中没有观察到的某些原生动物建立了其种类污染值     

环境外部不经济性内部化手段的评价与筛选

分析环境外部不经济性产生的根本原因,提出环境外部不经济性内在化手段的评价指标,并据此对国内外常环境外部不经济性内化手段作系统评价,评价结果表明,排污收费制度是当前最合理的环境外部不经济性内的在化手段。     

感潮河段污水处理厂尾水对受纳水体的水质影响研究

感潮河段污水处理厂尾水排放对受纳水体产生一定影响,利用二维水动力水质耦合模型,以COD、NH3-N、TP为污染因子,分别以正常排放和事故排放两种条件,模拟江苏南部某污水处理厂尾水排放,分析江段大小潮时污染物浓度增量情况。实验结果表明:正常排放,尾水对排放口附近江段保护区水质影响小;事故排放,尾水对保护区水质无影响,但长江水体影响范围增大,沿岸污染物浓度增高,且小潮周期影响作用强于大潮周期,污水处理厂应加强管理,尤其在小潮时应避免污水事故排放。     

Research progress on distribution,sources, identification,toxicity, and biodegradation of microplastics in the ocean,freshwater, and soil environment

• Microplastics are widely found in both aquatic and terrestrial environments. • Cleaning products and discarded plastic waste are primary sources of microplastics. • Microplastics have apparent toxic effects on the growth of fish and soil plants. • Multiple strains of biodegradable microplastics have been isolated. Microplastics (MPs) are distributed in the oceans, freshwater, and soil environment and have become major pollutants. MPs are generally referred to as plastic particles less than 5 mm in diameter. They consist of primary microplastics synthesized in microscopic size manufactured production and secondary microplastics generated by physical and environmental degradation. Plastic particles are long-lived pollutants that are highly resistant to environmental degradation. In this review, the distribution and possible sources of MPs in aquatic and terrestrial environments are described. Moreover, the adverse effects of MPs on natural creatures due to ingestion have been discussed. We also have summarized identification methods based on MPs particle size and chemical bond. To control the pollution of MPs, the biodegradation of MPs under the action of different microbes has also been reviewed in this work. This review will contribute to a better understanding of MPs pollution in the environment, as well as their identification, toxicity, and biodegradation in the ocean, freshwater, and soil, and the assessment and control of microplastics exposure.     

Discovery of emerging organic pollutants in the atmosphere through an omics approach

● We review the framework of discovering emerging pollutants through an omics approach. ● High-resolution MS can digitalize atmospheric samples to full-component data. ● Chemical features and databases can help to translate untargeted data to compounds. ● Biological effect-directed untargeted analyses consider both existence and toxicity. Ambient air pollution, containing numerous known and hitherto unknown compounds, is a major risk factor for public health. The discovery of harmful components is the prerequisite for pollution control; however, this raises a great challenge on recognizing previously unknown species. Here we systematically review the analytical techniques on air pollution in the framework of an omics approach, with a brief introduction on sample preparation and analysis, and in more detail, compounds prioritization and identification. Through high-resolution mass spectrometry (HRMS, typically coupled with chromatography), the complicated environmental matrix can be digitalized into “full-component” data. A key step to discover emerging compounds is the prioritization of compounds from massive data. Chemical fingerprints, suspect lists and biological effects are the most vital untargeted strategies for comprehensively screening critical and hazardous substances. Afterward, compressed data of compounds can be identified at various confidence levels according to exact mass and the derived molecular formula, MS libraries, and authentic standards. Such an omics approach on full-component data provides a paradigm for discovering emerging air pollutants; nonetheless, new technological advancements of instruments and databases are warranted for further tracking the environmental behaviors, hence to evaluate the health risk of key pollutants.     

活性炭纤维上4-氯酚及焦化废水尾水的O3催化氧化降解实验研究

选择YT-1000型活性炭纤维（ACF）作为催化剂,考察ACF与O₃协同作用催化降解水溶液中4-氯酚的最佳反应条件,并将该条件应用于焦化废水生物处理尾水中难降解有机污染物的催化氧化。ACF表面具有丰富的微孔结构,对4-氯酚有良好的吸附作用,在动力学上提高了其与O3反应的起始浓度,并且在ACF表面含氧、含氮等基团的催化作用下发生氧化反应,1 L浓度为100 mg/L的4-氯酚水样中投加2 g ACF反应6 min时,吸附作用对TOC的去除率为43.4%,而ACF协同O₃作用时的TOC去除率提高到72.5%,协同增效作用为67.1%;在选定的反应条件下,ACF协同O₃降解焦化废水生物处理尾水,60 min时的TOC与色度的去除率分别达到56.8%和96.3%。上述研究过程证明了吸附作用与催化作用的协同能有效降解生物过程不能降解的焦化废水中惰性有机污染物。     

温度和pH值对活性污泥法脱氮除磷的影响

温度和pH值是影响污水脱氮除磷效果的2个重要因素.试验采用连续搅拌槽式反应器(continuous stirred tank reactor,CSTR),通过对不同温度和pH值条件下的硝化、反硝化、释磷和吸磷反应速率的测定,总结出温度和pH值对活性污泥生化反应速率的影响规律.试验表明,硝化和反硝化速率随温度的升高而加快.在5℃和33℃时,硝化速率分别为0.01 kg NH4 -N/(kg VSS·d)和0.28 kg NH4 -N/(kg VSS·d);在5℃和30℃时,反硝化速率分别为0.097 kg NO3--N/(kg VSS·d)和0.476 kg NO3--N/(kg VSS·d);但温度对吸磷和释磷速率的影响不大.pH值对硝化、反硝化、吸磷和释磷速率均有显著影响,在pH值为7.74时,硝化速率为0.095 kg NO3--N/(kg VSS·d);而在pH值为4.9和10.08时,硝化速率仅为0.005 kg NO3--N/(kg VSS·d)和0.006 kg NO3--N/(kg VSS·d).在pH值为7.85时,反硝化速率达到最大值0.36 kg NO3--N/(kg VSS·d);而在偏酸性和碱性条件下,反硝化速率显著下降.