Air pollution characteristics and their relationship with emissions and meteorology in the Yangtze River Delta region during 2014–2016

With rapid economic growth and urbanization, the Yangtze River Delta(YRD) region in China has experienced serious air pollution challenges. In this study, we analyzed the air pollution characteristics and their relationship with emissions and meteorology in the YRD region during 2014–2016. In recent years, the concentrations of all air pollutants, except O_3,decreased. Spatially, the PM_(2.5), PM_(10), SO_2, and CO concentrations were higher in the northern YRD region, and NO_2 and O_3 were higher in the central YRD region. Based on the number of non-attainment days(i.e., days with air quality index greater than 100), PM_(2.5) was the largest contributor to air pollution in the YRD region, followed by O_3, PM_(10), and NO_2.However, particulate matter pollution has declined gradually, while O_3 pollution worsened.Meteorological conditions mainly influenced day-to-day variations in pollutant concentrations. PM_(2.5) concentration was inversely related to wind speed, while O_3 concentration was positively correlated with temperature and negatively correlated with relative humidity.The air quality improvement in recent years was mainly attributed to emission reductions.During 2014–2016, PM_(2.5), PM_(10), SO_2, NO_x, CO, NH_3, and volatile organic compound(VOC)emissions in the YRD region were reduced by 26.3%, 29.2%, 32.4%, 8.1%, 15.9%, 4.5%, and0.3%, respectively. Regional transport also contributed to the air pollution. During regional haze periods, pollutants from North China and East China aggravated the pollution in the YRD region. Our findings suggest that emission reduction and regional joint prevention and control helped to improve the air quality in the YRD region.     

不同雨强条件下太湖流域典型蔬菜地土壤磷素的径流特征

以太湖流域典型区域无锡市近郊区鸿声镇的蔬菜地为研究对象,采用人工模拟降雨的方法,通过野外径流小区试验,研究了不同雨强对菜地土壤磷素径流流失的影响.结果表明,初始产流时间随雨强的增大呈幂函数减小(R²=0.99),径流量在雨强较小时,缓慢上升,但随着雨强的增大急剧上升,在雨强0.83、1.17和1.67 mm·min^-1时,总磷(TP)和颗粒态磷(PP)都表现为初始流失浓度较高,随降雨历时延长略有下降,最终趋于稳定,而在大雨强2.50 mm·min^-1时,TP和PP呈现波浪式起伏,没有明显的变化趋势;在整个降雨-径流过程中,溶解态磷(DP)变化比较平缓,占TP的比例为20%～32%,而PP占TP的比例为68%～80%,其变化规律与TP相一致,由此可见,PP是土壤磷素流失的主要形态;通过对比不同雨强下不同形态磷素的流失率,发现TP的流失率,大雨强2.50 mm·min^-1是小雨强0.83 mm·min^-1的20倍,而DP的流失率,却是33倍,这表明随着雨强的增加,加速土壤PP流失的同时,也大大促进了DP的流失,主要原因是降雨前表施磷肥,使得磷肥中大量的无机态磷溶解释放到水环境中,增加了DP的流失,从而会加重受纳水体富营养化的程度.     

白洋淀不同类型水体表层沉积物重金属的赋存形态及风险

选取白洋淀中水道、沟壕、淀面和鱼塘这4种水体类型,采用改进的BCR提取法分析沉积物中Cd、Cr、Cu、Ni、Pb和Zn的形态特征,运用潜在生态风险指数、次生相与原生相（RSP）和风险评估编码（RAC）等方法对白洋淀沉积物重金属含量进行系统性的污染评估和生态风险评价.结果表明：①沉积物中重金属ω（Cd）、ω（Cu）和ω（Zn）均值分别为0.37、28.49和83.08 mg·kg^-1,分别有94.91%、73.91%和46.39%的点位超过土壤背景值.② Cd以非残渣态（F1+F2+F3）为主,质量分数范围为54%~97%,Cr以残渣态（F4）为主,质量分数为87%~99%.Cu、Ni、Pb和Zn主要以残渣态存在,但在非残渣态中Cu和Ni以可氧化态（F3）为主,Pb和Zn以可还原态（F2）为主.③基于RAC评价结果：Cd在水道、沟壕、开阔淀面和鱼塘分别有68.97%、39.89%、54.84%和49.78%的点位存在风险,而Cu、Ni和Pb等重金属风险较低.总体而言,白洋淀重金属总体污染水平较低,但在南刘庄片区的府河和白沟引河入河口等部分水道区域Cd存在生态风险和较高的生物可迁移性.     

贵州省部分地区土壤中酞酸酯类污染现状调查

对贵州省部分地区表层土壤中酞酸酯类的污染状况进行了调查。分别在遵义地区、黔南地区、黔东南地区和毕节地区采集483个土壤样品分析,结果表明,样品中酞酸酯总质量比(ΣPAEs)为未检出~8.22 mg/kg,均值为0.63 mg/kg。其中DEHP和DBP为主要污染物,均值分别为0.32 mg/kg和0.24 mg/kg,检出率分别为90.89%和97.10%。     

乙草胺和丁草胺在土壤中的移动性

利用土壤薄层层析法研究乙草胺和丁草胺在土壤中的移动性以灌溉河水为展开剂,得到乙草胺和丁草胺在北京海淀壤土中的相对移动值Rf的平均值分别为0.121和0.031,在河北白洋淀砂壤土中的相对移动值R_f的平均值分别为0.147和0.032.采用不同的土壤试验,乙草胺的移动性存在一定的差异.说明乙草胺在土壤中的移动性与土壤的性质有关,特别是土壤有机质含量,土壤吸附性能越强,越不易移动.乙草胺属于移动性弱的农药品种,移动等级为Ⅱ级,丁草胺属于移动性很弱的农药品种,移动等级为I级乙草胺和丁草胺虽然同属于酰胺类除草剂,但是,由于它们的水溶解度的差异,它们在土壤中的移动性有较大的差别.以30mg·L^-1的阴离子表面活性剂十二烷基苯磺酸钠水溶液(DDBS)和阳离子表面活性剂十六烷基三甲基溴化铵(HDTMA)为展开剂,乙草胺在北京海淀壤土中的R_f的平均值分别为0.159和0.098.阴离子表面活性剂能够促进农药在土壤中的迁移,阳离子表面活性剂能够促进农药在土壤中的吸附,从而阻止农药在土壤中的迁移.     

水生植物对面源污水净化效率研究

于自然条件下研究了慈茹、菱白等7种水生植物对面源污水的净化率。结果表明,7种试验植物对水体中N、P均有很高的净化率,其中以慈茹和菱白的综合净化率为最高。由于不同植物对N、P的净化率不同,所以多种植物配置可提高植物对面源污水的综合净化率。     

3株溶藻细菌的分离鉴定及其溶藻效应

从武汉市的池塘分离到3株编号分别为M6,M8和M13的溶藻细菌,对这3株细菌的生理生化特性、溶藻专一性和溶藻原因进行了研究.结果表明:M6,M8和M13分别属于葡萄球菌属(Staphylococcus sp.)、芽孢杆菌属(Bacillus sp.)和节杆菌属(Arthrobacter sp.);它们分别能溶解鲍氏织线藻、念珠藻、鱼腥藻、坑形席藻、铜绿微囊藻、鞘丝藻等多种蓝藻,并且它们的液体溶藻现象较固体溶藻现象明显;3株溶藻细菌培养液的过滤液仍有溶藻效应,说明溶藻原因可能是细菌释放某种化学物质所致.      

Photodegradation of acetochlor in water and UV photoproducts identified by mass spectrometry

The sunlight photodegradation half-lives of 20 mg/L acetochlor were 151, 154 and 169 days in de-ionized water, river water and paddy water, respectively. When exposed to ultraviolet (UV) light, acetochlor in aqueous solution was rapidly degraded. The half-lives were7.1, 10.1, and 11.5 min in de-ionized water, river water and paddy water, respectively. Photopreduets of acetochlor were identified by gas chromatography/mass spectrometry(GC/MS) and found at least twelve photoproducts resulted from dechlorination with subsequent hydrtrxylation and cyclization processes. The chemical structures of ten photoproducts were presumed on the basis of mass spectrum interpretation and literature data. Photoproducts are identified as 2-ethyl-6-methylaniline; N, N-diethylaniline ; 4, 8-dimethyl-2-oxo- 1,2,3,4- tetrahydroquino-line; 2-oxo-N-(2-ethyl-6-methylphenyl)-N-(ethoxymethyl) acetamide; N-(ethoxymethyl)-2‘-ethyl-6‘-methylformanilide; 1-hydroxyaeetyl-2-ethoxyl-7-ethylind ole; 8-ethyl-l-ethoxymethyl-2-oxo-1, 2, 3, 4-tetrahydroquinoline; 4, 8-dimethyl-l-ethoxymethyl-2-oxo-1, 2, 3, 4-tetrahydroquinoline; 2-hydroxy-2‘-ethyl-6‘-methyl-N-(ethoxymethyl) acetanilide and a compound related to acetochlor. The other two photoproducts were detected by GC/MS although their chemical structure was unknown.     

环境承载力的本质及其定量化初步研究

环境承载力描述了环境系统对人类活动支持能力的阈值,是环境系统功能的外在表现,是包含时间、空间和经济行为等自变量的函数。通过环境承载力指标体系及其综合值的计算可以描述实际环境承载量和环境承载力的大小,通过环境承载率（环境承载量／环境承载力）的计算可反映环境承载力的超载状况或环境与经济的协调程度。并以实例对环境承载力进行分析。