洱海流域农业面源污染空间分布特征及分类控制策略

作为典型的高原坝区农业型流域,洱海流域农业面源污染严重,威胁洱海水质.以洱海流域为研究对象,综合数理分析及GIS技术,开展流域农业面源污染负荷分析及评价,使用排污系数法估算了2018年洱海流域农村生活、畜禽养殖业和种植业污染中COD（化学耗氧量）、TN（总氮）、TP（总磷）的排放负荷,并通过等标污染负荷法在GIS空间分析反映流域内污染排放分布情况.结果表明:①2018年洱海流域农业面源主要污染物COD、TN、TP的排放量分别为11 188.20、2 752.56和259.33 t.COD排放量主要来自畜禽养殖,TN与TP的排放量均主要来自种植业.②洱海流域农业面源主要污染物COD、TN、TP等标污染负荷分别为559.41、2 752.56和1 296.63 m3/a.种植业等标污染负荷在总等标污染负荷中的占比最高,为36.40%,其次是畜禽养殖业,为34.44%.③各乡镇的等标污染负荷差异较大,等标污染负荷范围为（286.16±150.67）m3/a,等标污染负荷强度范围（0.13±0.067）m3/a.④聚类分析结果表明,洱海流域农业面源污染可分为种植业主导型、种植业高污染型、生活污染主导型和畜禽养殖业主导高污染型等4种类型.研究显示:来源于种植业的面源污染是洱海流域水环境保护需要控制的首要污染源,TN是需要控制的首要污染物;排放量与等标污染负荷的空间分布特征均呈流域北部乡镇污染物排放量较高,但流域西部各乡镇排放强度较大的特征;流域内各乡镇防治面源污染需要针对其污染来源特点分别采取推进种养平衡、推广绿色种植、分区控制农田径流以及推进农村生活污水治理等分类控制策略.      

Chemical formation and source apportionment of PM2.5 at an urban site at the southern foot of the Taihang mountains

The region along the Taihang Mountains in the North China Plain (NCP) is characterized by serious fine particle pollution. To clarify the formation mechanism and controlling factors, an observational study was conducted to investigate the physical and chemical properties of the fine particulate matter in Jiaozuo city, China. Mass concentrations of the water-soluble ions (WSIs) in PM_2.5 and gaseous pollutant precursors were measured on an hourly basis from December 1, 2017, to February 27, 2018. The positive matrix factorization (PMF) method and the FLEXible PARTicle (FLEXPART) model were employed to identify the sources of PM_2.5. The results showed that the average mass concentration of PM_2.5 was 111 μg/m³ during the observation period. Among the major WSIs, sulfate, nitrate, and ammonium (SNA) constituted 62% of the total PM_2.5 mass, and NO₃^? ranked the highest with an average contribution of 24.6%. NH₄⁺ was abundant in most cases in Jiaozuo. According to chemical balance analysis, SO₄^2?, NO₃^?, and Cl^? might be present in the form of (NH₄)₂SO₄, NH₄NO₃, NH₄Cl, and KCl. The liquid-phase oxidation of SO₂ and NO₂ was severe during the haze period. The relative humidity and pH were the key factors influencing SO₄^2- formation. We found that NO₃^? mainly stemmed from homogeneous gas-phase reactions in the daytime and originated from the hydrolysis of N₂O₅ in the nighttime, which was inconsistent with previous studies. The PMF model identified five sources of PM_2.5: secondary origin (37.8%), vehicular emissions (34.7%), biomass burning (11.5%), coal combustion (9.4%), and crustal dust (6.6%).     

施用磷酸盐和沸石对土壤镉形态转化的影响

本试验在室内模拟外源Cd污染土壤,研究了磷酸二氢钾、磷酸氢二铵和沸石单独施用,以及沸石和磷酸氢二钾、沸石和磷酸氢二铵二者配施,对Cd污染土壤形态变化的影响.结果表明,施用不同改良剂后,土壤交换态Cd含量出现不同程度降低,而碳酸盐结合态、铁锰氧化物结合态、有机结合态和残渣态Cd含量增加.与对照相比,单独施用磷酸二氢钾、磷酸氢二铵和沸石,以及沸石和磷酸氢二钾配施、沸石和磷酸氢二铵配施分别使土壤有效Cd含量降低25.2%~51.7%、21.6%~46.8%、6.4%~23.2%、38.6%~61.4%和34.1%~56.4%.各处理均能提高土壤速效磷含量,且土壤速效磷含量与有效态Cd含量呈极显著负相关,相关系数r=-0.902 6,各处理之间土壤p H值与有效态Cd含量存在负相关关系.由此可知,在施用磷酸盐和天然沸石条件下,土壤速效磷含量的变化是降低土壤镉有效性的主要因素.     

酸性矿山废水天然中和形成的富铁沉淀及其环境属性

采集了云南王家滩铁矿的酸性矿山排水及其与溪流中和后的溪水与沉积物, 运用谱学及电子显微分析等方法,对采集样品的化学及矿物学等方面的特征进行了分析. 结果表明, 王家滩铁矿的酸性矿山排水在与未污染溪水中和时, 酸度和电导率均显著降低, 但元素的浓度变化不很一致, 沿水流方向,除Fe3+、SO2-4、 Ca2+等少数元素, 大多数元素的浓度都未发生明显的降低. 中和成因沉淀物具有富铁的特征,矿物组成以水铁矿为主, 此外在下游沉积物中还见有少量针铁矿及纤铁矾. 其中上游中和区水铁矿以2线水铁矿为主, 下游以6线水铁矿为主. 而各处沉积均具有明显的分层特征,且均为外层以2线水铁矿为主, 内层以6线水铁矿及针铁矿为主. 以水铁矿为主要矿物的中和沉积物对各种有毒有害元素具有较强的吸持作用. 对这些结果的进一步分析表明, 在成因上,pH值和SO2-4的浓度共同控制了水铁矿的形成;在重(类)金属吸持方面,水铁矿的迁移及相应的对AMD中重(类)金属的自净化作用受中和区域的水动力条件影响较大.     

南四湖沉积物中二噁英类化合物的分布

用1 3C同位素内标法 ,高分辨率气相色谱 高分辨率质谱对南四湖表层沉积物中 1 7种含 2 3 7 8 氯代二苯并二英 /呋喃 (PCDD/Fs)及 1 2种共平面多氯联苯 (Co PCBs)的含量、同系物异构体的分布特征、沉积通量、毒性当量及来源进行了初步分析 ,并与山东近海 (日照、烟台、青岛 )的测定结果进行比较 .总Co PCBs含量分别为 5 4 4pg·g- 1 dw (南阳湖 )和 41 4pg·g- 1 dw (微山湖 ) .总PCDD/Fs含量分别为 1 0 6 7pg·g- 1 dw (南阳湖 )和1 47 0pg·g- 1 dw (微山湖 ) .两湖含 2 3 7 8 PCDD/Fs异构体对总毒性当量浓度的贡献基本相同 ,即以四—五氯代异构体为主 .PCDD/Fs含量次序为青岛 >日照 >南四湖 >烟台 .南四湖、日照、烟台近海沉积物中的PCDD/Fs对总TEQ (PCDD/F TEQ PCB TEQ)的贡献为68 8%— 93 0 % .南四湖与山东近海沉积物中PCDDs/PCDFs比值和OCDD %∑百分比表明 ,山东省PCDD/Fs的来源较为一致 ,相对恒定 .除河口处外 ,大气沉降应是南四湖及山东近海PCDD/Fs的主要来源 .     

Phosphorus release potential and pollution characteristics of sediment in downstream Nansi Lake, China

The research aimed to evaluate present and potential phosphorous pollution due to high sedimentary phosphorus load and release from sediment, when external phosphorus was reduced in downstream Nansi Lake. Pollution load of the sediment and overlying water was investigated. Kinetics and isotherms of adsorption/release of sedimentary phosphorus were studied to determine equilibrium phosphate concentration (EPC₀) and release potential. Kinetics of phosphorus adsorption on sediment and release from sediment were well described by both the pseudo-first-order rate equation and the pseudo-second-order rate equation, but more appropriate to the pseudo-second-order rate equation with the adsorption/release capacity more close to the measured values, suggesting that the processes were chemically rate controlled and dependent on adsorption capacity. Soluble reactive phosphorus (SRP) sorption isotherms on sediment were best fitted by the modified Langmuir model indicating a monolayer adsorption. By comparing EPC₀ and SRP of water, the status (adsorption, releasing or in equilibrium) of sediment phosphorus could be determined. The sediments at site S1, S3, S4, S5, and S7 where the EPC₀s were greater than the SRPs, had a potential to release phosphorus into the water column. However, those sediments at S9, S10, and S12, where the EPC₀s were approximately equal to the SRPs, were in impermanent equilibrium with overlying water in status of phosphorus, the sediments can be likely to release phosphorus to the water column once the equilibrium was broken. Therefore, sedimentary phosphorus can be a secondary pollution source in downstream Nansi Lake.     

电镀厂污染土壤重金属形态及淋洗去除效果

以某电镀厂污染场地重污染区域土壤为研究对象,对土壤中重金属全量和各形态含量进行分析,并研究筛选高效土壤淋洗剂,比较其淋洗去除效果。结果表明,该土壤以铬和镍污染最为严重,土壤铬和镍含量分别达1 564.00和679.00 mg.kg-1,土壤铜、锌和铅含量分别为297.00、276.00和51.40 mg.kg-1,铜、铬、镍、锌和铅的有效态比例分别为41.77%、13.16%、28.08%、21.50%和31.18%。去离子水、盐酸、乙酸、草酸、柠檬酸和EDTA 6种淋洗剂中,去离子水对5种重金属提取量均较少;草酸对铜、铬、镍和锌去除效果较好,去除率分别为55.1%、24.8%、47.5%和29.3%;柠檬酸对铜、铬、镍和锌去除效果较好,去除率分别为26.3%、25.7%、33.0%和21.6%;EDTA对铜、镍、锌和铅去除效果较好,去除率分别为31.5%、28.9%、21.4%和30.6%。综合考虑淋洗剂的提取效果、水溶性以及操作难度和成本,建议采用柠檬酸作为淋洗剂,最佳液土比〔V（液）∶m（土）〕为10∶1,最佳淋洗时间为6 h。     

助溶剂甲苯和二甲基亚砜对斑马鱼胚胎发育的复合毒性效应

研究了甲苯和二甲基亚砜(DMSO)对斑马鱼胚胎生长、发育的毒性效应.实验结果表明:低剂量的甲苯(0.05%)单一暴露对斑马鱼胚胎发育有一定毒性,DMSO(0.45%)对斑马鱼胚胎无明显毒性;但甲苯与DMSO具有较强的复合毒性效应,随着DMSO含量的增加,与甲苯单一暴露组相比,斑马鱼胚胎死亡率显著增加、胚胎孵化率下降、胚胎发育迟缓并生成大量畸形;但甲苯以及甲苯和DMSO复合物对人胚肾HEK-293细胞株和人胃癌SGC-7901细胞株的活力均没有明显效应.DMSO可通过提高甲苯在水中的分散性,增加甲苯的神经毒性,但对离体实验模型无显著效应,故在选择不同生物模型评估有机污染物毒性效应时,需考虑不同类型助溶剂所产生的复合效应,以减少实验误差.     

土地利用对湿地土壤活性有机碳的影响研究进展

湿地生态系统土壤碳库的周转及碳源/汇过程对全球气候变化起着极其重要的作用,而土壤碳库中的活性碳组分对环境因子变化响应最为敏感,湿地土壤活性有机碳在湿地土壤碳、氮、磷等养分元素的生物地球化学循环方面起着十分重要的作用。不同的土地利用方式对湿地土壤活性有机碳组分的特征分布影响显著,综述了土壤活性有机碳内涵、组分及土地利用方式变化对湿地土壤活性有机碳多种组分的影响研究进展,展望不同土地利用方式下湿地土壤活性碳库的未来研究方向,并提出今后应加强不同土地利用方式下湿地生态系统土壤活性碳库与土壤微生物及土壤酶活性的关系研究,以期为评估湿地生态系统碳源/汇功能提供理论基础。     

五种农药对三唑酮光解的影响

本文研究了氯氰菊酸，溴氰菊酯，多菌灵，γ－六六六及辛硫磷等五种农药对杀菌剂三唑酮光化学降解的影响，当三唑酮分别与这五种农药以等剂量混合光照后，三唑酮的光解速度加快１．４４－２．４２倍，表现了较强的光敏降解效应，其敏化光解效率我照时间延长而逐渐提高，当三唑酮分别与这五种农药以２：１剂量比混合光照后，仅溴氰菊酯．多菌灵表现敏化降解效应，而氯氰菊酯，γ－六六六及辛硫磷则显示光猝灭降解效应，五种农药对三唑