基于实测光谱与MODIS数据的太湖悬浮物定量估测

以太湖为研究区域,对太湖水体的水面反射光谱进行实地测试,并取样在实验室进行水质分析;根据光谱分析得到的悬浮物特征波段,估测悬浮物浓度;最后,对比MODIS波段,用最敏感波段及主成分分析法建立悬浮物估测模型.结果表明,576nm附近的反射率峰值、841nm处反射率一阶微分值和808nm附近的反射峰高与悬浮物浓度都有较好的相关性,其中峰高法和一阶微分法对悬浮物浓度的估测精度相当;MODIS波段1与悬浮物浓度相关性最好,经过主成分变化后的第一主成分和第二主成分可以较好地估测悬浮物浓度.因此,可利用MODIS数据对太湖悬浮物进行长期动态监测.     

厦门海域水体悬浮物遥感反演算法研究

通过现场实测厦门海域水体遥感反射率及水体悬浮物浓度,分析了该海域水体的遥感反射光谱特征,选取了特征波段及组合建立了该海域水体悬浮物浓度反演模型。本文经过对比分析水体中呈悬浮态的总颗粒物质量浓度的不同反演方法,最后得出悬浮颗粒物在近红外波段的反射曲线的反射率高值和低值围成的区域面积可较好的反演研究区域的悬浮颗粒物浓度,其统计回归模型的决定系数是0.66,该反演算法的RMSE是10.25mg/L,相对误差是7.79mg/L。     

基于实测光谱的杭州湾悬浮物浓度遥感反演模式

悬浮物是我国近海水质遥感监测的主要参数之一.利用ASD地物光谱仪测量杭州湾水体的反射光谱,同步采集表层水样获取悬浮物浓度,模拟水色卫星MODIS和MERIS的波段设置提取遥感反射率,基于人工神经网络分别建立2种悬浮物浓度的遥感反演模式.实测结果表明,杭州湾水体中悬浮物浓度较高,泥沙含量远远大于叶绿素浓度,平均值分别为705 mg/L和1.164 mg/m³;2个监测站位的悬浮物浓度表现出时空上的差异,尤其是随潮汐变化的短周期变异十分显著;实测水体反射率光谱曲线在650～700 nm之间与800 nm附近分别出现峰值,光谱曲线一阶微分结果显示第一反射峰的位置随着悬浮物浓度增大向长波方向移动.基于神经网络建立的模拟算法充分利用了卫星不同通道的光谱信息,可以同时模拟水体中色素与非色素悬浮物的浓度,模型取得了较好的拟合效果,R²均大于0.95,可以应用于实际卫星遥感反演,尤其是MERIS数据,因其具有相对较高的空间分辨率,在近海水环境遥感监测中的应用前景更为广阔.     

基于QAA算法的巢湖悬浮物浓度反演研究

QAA(quasi-analytical algorithm)算法基于辐射传输原理,估算水体后向散射系数,是目前较为成熟的半分析模型方法.2009年6月对巢湖水体进行野外实测,在获得遥感反射率、吸收衰减系数、悬浮物浓度(cTSM)等数据的基础上,构建了巢湖水体cTSM的近红外双波段反演模型,并将QAA算法计算得到的后向散射概率作为输入,以期提高cTSM的反演精度.结果表明,①对巢湖水体而言,807 nm和834 nm是构建近红外双波段模型的最佳波段,807 nm处的单位散射系数为0.411 m2.g-1,834 nm处的单位散射系数为0.395 m2.g-1;②利用QAA算法计算得到的巢湖水体的后向散射概率为0.029,将该值输入反演模型后,cTSM的反演精度与输入其他经验值相比得到明显提高,反演值与实测值的均方根误差RMSE和平均相对误差绝对值MAPE分别达到12.143 mg.L-1和24.378%;③在cTSM较高的站点(近似高于30 mg.L-1),利用近红外双波段模型反演的悬浮物浓度结果更为稳定和可靠.     

基于Sentinel-3 OLCI影像的秦皇岛海域悬浮物浓度遥感反演

基于2013~2021年期间秦皇岛海域遥感反射率、悬浮物浓度及叶绿素a浓度等实测数据,开展了该海域Sentinel-3 OLCI影像的悬浮物浓度遥感反演模型研究.结果表明,文献中常用的典型经验模型形式均不适用于秦皇岛海域,以490、620及708.75nm为悬浮物反演的敏感波段,以560nm为参比波段,将各敏感波段与参比波段的比值作为自变量,最终建立了适用于秦皇岛海域的Sentinel-3 OLCI四波段悬浮物浓度遥感反演模型（R²=0.69,MAPE=24.79%,RMSE=2.82mg/L）;并采用2021年7月24日Sentinel-3 OLCI影像进行悬浮物浓度遥感反演产品的真实性检验,得到反演值与实测值的平均相对误差为13.24%.将上述四波段模型用于2021年1~12月秦皇岛海域的Sentinel-3 OLCI影像,反演得到月均悬浮物浓度,发现秦皇岛海域悬浮物浓度整体呈现沿岸海域高、离岸海域低,秋冬季高、春夏季低的时空变化特征;且2018~2021年秦皇岛海域悬浮物浓度的年均值逐年递减,水体越来越澄清.     

太湖水体上行漫射衰减系数的变化特征研究

水体上行漫射衰减系数是反映水体中上行光强衰减的重要光学参数,它直接影响着水下光场分布,对水环境生态系统变化具有重要意义.然而,对于太湖水体而言,上行漫射衰减系数的变化特征尚不明确.为此,本课题组于2010年4月29日到5月2日对太湖水体28个采样点进行了野外原位观测,获取了相应的水体光学参数和水质参数数据集.在分析水体上行衰减系数光谱特征和空间分布特征的基础上,对其与太阳高度角、悬浮物浓度和叶绿素浓度之间的关系进行了研究.结果表明,上行漫射衰减系数的光谱特征表现为短波蓝光部分衰减系数较大,长波红光部分衰减系数较小,且衰减系数在575~700 nm之间随着波长的增加变化不明显,在675 nm附近出现相对高值,其与叶绿素a浓度存在显著的相关关系(r=0.574,n=28,p<0.05).下行与上行漫射衰减系数随波长的变化特征大致相似,其差值谱线的变化规律为:小于400 nm的范围内,呈线性减小;在400~800 nm之间除760 nm附近有一峰值外,其余部分基本无明显变化;大于800 nm时,又迅速增加.上行衰减系数在不同湖区的空间分布大致为:开阔水域区>草型湖区>典型藻型湖区>草、藻过渡型湖区,藻型和草、藻过渡湖区在675 nm附近的峰值皆较为明显.上行衰减系数基本上随太阳高度角的增大而减小,上行漫射衰减系数与悬浮物浓度的偏相关性最好(r=0.963,n=28,p<0.05),太阳高度角次之(r=0.474,n=28,p<0.05),叶绿素浓度的最低(r=0.175,n=28,p<0.05).     

太湖、巢湖水体总悬浮物浓度半分析反演模型构建及其适用性评价

总悬浮物浓度是水体重要的水质参数.本研究利用太湖春季、秋季和巢湖夏季多期野外实测数据,通过对生物光学模型进行合理的简化构建适用于太湖、巢湖水体总悬浮物浓度反演的半分析模型,并将该模型应用于MERIS和环境一号卫星高光谱卫星影像上以验证该方法的适用性.结果表明:①针对太湖和巢湖水体,总悬浮物浓度最优反演波段范围为730～832nm(氧气吸收带除外);②针对MERIS数据,波段10(中心波长754 nm)和波段12(中心波长779 nm)均适用于太湖总悬浮物浓度反演,而波段11(中心波长761 nm)由于氧气吸收带的影响不适用于总悬浮物浓度反演;③针对太湖MERIS数据,模型反演结果的相对误差基本上呈现出随距离卫星过境时间增大而逐渐增加的趋势,在卫星过境时间正负3 h内测量的样点,模型反演结果的相对误差均在50%以内,而时间差超过3 h,相对误差则逐渐增大到50%以上;④环境一号卫星高光谱数据17个波段(B83～B99)均能够对巢湖总悬浮物浓度进行较好的反演,其反演效果要好于MERIS数据在太湖的反演结果.     

长江干流表层水体悬浮物的空间变化特征及遥感反演

总悬浮物（TSM）是描述水体光学特性和污染程度的一个重要参数,利用遥感技术准确获取面状水域悬浮物浓度的信息,可有效地对水体浑浊程度、污染程度等信息指标进行高效监测分析,解决观察范围小、不方便以及数据获取难等难题.以野外实测水体高光谱数据和悬浮物浓度及其组分等数据,参照MODIS （1~4波段）、Landsat 8（1~5波段）、Sentinel 2（2~6波段）和HJ-B1（1~4波段）等常用波段范围,构建长江干流（重庆-上海段）水体TSM的半经验模型,从而检验、比较常用卫星对河流水体TSM的反演潜力.结果表明：①枯水期长江干流浊度和TSM从重庆到上海整体程增加趋势,相反有机悬浮物浓度在总悬浮物浓度中所占的比例（OSM/TSM）从重庆到上海整体呈现较小趋势.②水体光谱曲线基本没用叶绿素a的光谱特征（700 nm附近的反射峰）,而是展现出悬浮物浓度占主导因素的双峰型光谱特征.由于水体中悬浮物浓度较低（<114.68 mg ·L^-1）,第一峰值明显高于第二峰值,但反射峰位置具有明显的向波长方向移动的"红移"现象.③长江干流水体的反射率对悬浮物浓度最敏感的波段是600~710 nm和475~550 nm波段,这些波段大部分都落在MODI、Landsat 8,Sentinel 2和HJ-1B卫星绿波段和红波段内,因此目前常用卫星的波段设置在反演长江干流水体TSM上都具有一定的潜力.其中Sentinel 2卫星波段设置最合适长江干流水体悬浮物浓度的反演,其最佳的指数反演模型RMSE为10.23mg ·L^-1,MAPE为23%.     

基于多源同步数据的闽江下游悬浮物定量遥感

利用2006-09-18的同步Landsat TM数据、水面实测光谱数据和现场水样数据,研究了闽江下游的悬浮物,在这3种同步数据的基础上建立了分别基于实测光谱与影像光谱的悬浮物遥感预测模型.结果表明,实测光谱数据在690nm波长处,归一化光谱反射率与悬浮物浓度达到最大正相关,由690nm和530nm二处的反射率构成的比值预测模型与实测悬浮物浓度的拟合精度最高,最佳拟合模型可表达为SS=116.2(R690/R530)-33.4.TM影像各波段中以(TM2 TM3)2波段组合与实测悬浮物浓度的相关性最佳.由其所建立的影像光谱预测模型与实测悬浮物浓度的拟合精度最高.最佳拟合模型可表达为SS=3793.7(RTM3 RTM2)2-16.5.模型的精度评价表明,实测光谱模型的预测能力要强于影像光谱模型.但二者差异不大.在缺乏地面实测光谱数据时.基于影像光谱的遥感定量模型仍不失为一种预测悬浮物浓度的有效方法,其对闽江下游悬浮物浓度的反演结果能较准确地反映出该区域悬浮物浓度分布的空间差异,具有较高的实用性.     

基于Sentinel-2 MSI影像的河湖系统水体悬浮物空间分异遥感监测:以安徽省升金湖与连接长江段为例

开展河湖系统悬浮物监测对掌握水体泥沙运移规律、制定水环境治理措施具有重要意义.以安徽省升金湖与连接长江段水体为研究区,根据实测光谱模拟Sentinel-2 MSI影像波段反射率,结合同步水体悬浮物实测数据建立反演模型;而后根据2017～2019年28景MSI影像水体悬浮物反演结果,分析河湖系统水体悬浮物浓度的变化规律,并探究水位变化对其空间分异的影响.结果表明:①根据MSI影像第六波段与第三波段的比值建立的二次多项式模型具有较高的反演精度(R~2=0.863,RMSE=22.211 mg·L~(-1)),适用于高浊度水体悬浮物反演;②在空间上,升金湖入湖口附近、上中湖区西北部和下湖悬浮物浓度相对较高,除夏季外升金湖悬浮物浓度均高于其连接长江段;在时间上,升金湖悬浮物浓度在夏季相对较低,在其他季节较高,而与其连接的长江水体呈现相反的年内变化规律;③闸控影响下河湖连通性改变造成的水位变化,是影响升金湖-长江悬浮物空间分异的关键因素.在平水期与枯水期,升金湖对长江悬浮物浓度变化具有一定的贡献度,而在丰水期,升金湖与长江悬浮物浓度变化之间的相关性不明显.     

Distribution and ecological effect of mercury in Laogang landfill, Shanghai, China

Laogang landfill near Shanghai is the largest landfill in China, and receives about 10000 t of daily garbage per day, Samples of topsoil and plants were analyzed to evaluate mercury pollution from the landfill. For topsoil samples, there were significant correlations among total mercury （HgT）, combinative mercury （Hgc） and gaseous mercury （HgG）, and content of total organic carbon （TOC）, but, no significantly relationship was found between Hg content and filling time. Hg content changes in vertical profiles with time showed that the average Hgv of profiles 1992, 1996, and 2000 was similar, but their average HgG was quite different. HgT was significantly correlated with Hgc in profile 1992 and 2000, and Hgv was significantly correlated with Hg6 in profile 1996. HgG/Hgv ratio in profile samples decreased in the order of （HgG,/HgT）1992〉（HgG/HgT）1996〉〉（HgG/HgT）2000. A simple outline of Hg release in landfill could be drawn： with increasing of filling time, degradation undergoes different biodegradation, accordingly, gaseous mercury goes through small, more, and small proportion to total mercury. Distribution of Hg in plants was inhomogeneous, following the order of leaf〉root〉stem. The highest value of leaf may be associated with higher atmospheric Hg from landfill. Ligneous plants （e.g. Phyllostachys glanca, Prunus salicina and Ligustrum lucidum） are capable of enriching more Hg than herbaceous plants.     

EDTA-enhanced phytoremediation of lead contaminated soil by Bidens maximowicziana

Phytoremediation is a potential cleanup technology for the removal of heavy metals from contaminated soils.Bidens maximowicziana is a new Pb hyperaccumulator,which not only has remarkable tolerance to Pb but also extraordinary accumulation capacity for Pb.The maximum Pb concentration was 1509.3 mg/kg in roots and 2164.7 mg/kg in overground tissues.The Pb distribution order in the B. maximowicziana was:leaf>stem>root.The effect of amendments on phytoremediation was also studied.The mobility of soil Pb and the Pb concentrations in plants were both increased by EDTA application.Compared with CK(control check),EDTA application promoted translocation of Pb to overground parts of the plant.The Pb concentrations in overground parts of plants was increased from 24.23-680.56 mg/kg to 29.07-1905.57 mg/kg.This research demonstrated that B.maximowicziana appeared to be suitable for phytoremediation of Pb contaminated soil,especially,combination with EDTA.     

Decomposition of alachlor by ozonation and its mechanism

Decomposition and corresponding mechanism of alachlor, an endocrine disruptor in water by ozonation were investigated. Results showed that alachlor could not be completely mineralized by ozone alone. Many intermediates and final products were formed during the process, including aromatic compounds, aliphatic carboxylic acids, and inorganic ions. In evoluting these products, some of them with weak polarity were qualitatively identified by GC-MS. The information of inorganic ions suggested that the dechlorination was the first and the fastest step in the ozonation of alachlor.     

Enzymatic oxidation of aqueous pentachlorophenol

The influence of the nonionic surfactant Tween 80 on pentachlorophenol （PCP） oxidation catalyzed by horseradish peroxidase was studied. The surfactant was tested at concentrations below and above its critical micelle concentration （CMC）. Enhancement of PCP removal was observed at sub-CMCs. The presence of Tween 80 in the reaction mixture reduced enzyme inactivation which occurred through a combination of free radical attack and sorption by precipitated products. A simple first-order model was able to simulate time profiles for enzyme inactivation in the presence or absence of Tween 80. At supra-CMCs, the surfactant caused noticeable reductions in PCP removal, presumably through micelle partitioning of PCP which precluded the hydrophobic PCP molecule from interacting with the enzyme.     

基于综合水质标识指数和对应分析法的校园河道水质评价

以三峡大学的校园河道求索溪为研究对象,利用综合水质标识指数法确定求索溪水质类别,分析其水质时空变化规律,并利用对应分析法得出求索溪中不同监测点的主要污染因子.研究结果表明:求索溪整体的综合水质标识指数为7.423,整体水质为劣V类(地表水环境质量标准GB 3838-2002)且黑臭.从时间变化来看,求索溪4月份的水质最差,5月份次之,4、5月份所有监测点的水质都劣于V类且黑臭;8月份水质最好,水质为Ⅳ类;从空间分布来看,8个监测点综合水质标识指数均超过6.0,水质为劣V类,其中6号监测点的水质相对最好,监测点3号的水质相对最差;对应分析法得出求索溪的整体水体污染程度受总氮因子的影响最大,其次为总磷.该研究拟为求索溪及类似校园河道的水环境治理研究提供基础依据和参考.     

Effects of chitosan on growth of an aquatic plant (Hydrilla verticillata) in polluted waters with different chemical oxygen demands

Effects of chitosan on a submersed plant, Hydrilla verticillata, were investigated. Results indicated that H. venicillata could prevent ultrastructure phytotoxicities and oxidativereaction from polluted water with high chemical oxygen demand (COD). Superoxide dismutase (SOD) activity and malondialdehyde (MDA) contents in H. verticillata treated with 0.1% chitosan in wastewater increased with high COD (980 mg/L) and decreased with low COD (63 mg/L), respectively. Ultrastructural analysis showed that the stroma and grana of chloroplast basically remained normal. However, plant cells from the control experiment (untreated with chitosan) were vacuolated and the cell interval increased. The relict of protoplast moved to the center, with cells tending to disjoint. Our findings indicate that wastewater with high COD concentration can cause a substantial damage to submersed plant, nevertheless, chitosan probably could alleviate the membrane lipid peroxidization and ultrastructure phytotoxicities, and protect plant cells from stress of high COD concentration polluted water.     

Removal of cadmium using MnO2 loaded D301 resin

MnO2 loaded weak basic anion exchange resin D301 （Anion exchange resin, macroreticular weak basic styrene） as adsorbent has been prepared and applied to the removal of cadmium. The adsorption characteristics have been investigated with respect to effect of pH, equilibrium isotherms, removal kinetic data, and interference of the coexisting ions. The results indicated that the Cd^2＋ could be efficiently removed using MnO2 loaded D301 resin in the pH range of 3-8 from aqueous solutions with the co-existence of high concentration of alkali and alkaline-earth metals ions. The saturate adsorption capacity of the Cd^2＋ was 77.88 mg/g. The adsorption process followed the pseudo first-order kinetics. The equilibrium data obtained in this study accorded excellently with the Langmuir adsorption isotherm.     

Effect of coagulation pretreatment on the fouling of ultrafiltration membrane

The purpose of this study is to understand the effect and mechanism of preventing membrane fouling, by coagulation pretreatment, in terms of fractional component and molecular weight of natural organic matter （NOM）. A relatively higher molecular weight （MW） of hydrophobic compounds was responsible for a rapid decline in the ultrafiltration flux. Coagulation could effectively remove the hydrophobic organics, resulting in the increase of flux. It was found that a lower MW of neutral hydrophilic compounds, which could remove inadequately by coagulation, was responsible for the slow declining flux. The fluxes in the filtration of coagulated water and supernatant water were compared and the results showed that a lower MW of neutral hydrophilic compounds remained in the supernatant water after coagulation could be rejected by a membrane, resulting in fouling. It was also found that the coagulated flocs could absorb neutral hydrophilic compounds effectively. Therefore, with the coagulated flocs formed on the membrane surface, the flux decline could be improved.     

Penetration analysis of elements and bioleaching treatment of spent refractory for recycling

Acidithiobacillus ferrooxidans ATCC23270 and Acidithiobacillus thiooxidans TM-32 were used for bioleaching of spent refractories of aluminium and copper melting furnaces for their recycling.Firstly,penetration of elements into aluminium melting furnace refractory was investigated and it was found that up to 7 cm from surface was contaminated.Comparison on leaching efficiency by the strains ATCC23270 and TM-32 found that the strain ATCC23270 could treat larger amount of the refractories than the strain TM-32 could do.In the experiment of bioleaching of spent refractory aluminium melting furnace by the strain ATCC23270,high leaching efficiency were obtained on Al,Si,and Ca,and extremely low leaching performance was,however,shown on the rest of elements i.e.,Na,Mn,and Zn.Under the strain TM-32 use,relatively high leaching performance was recognized on Al,Si,Ca,Na,Mn,and Zn.In the experiment of bioleaching for spent refractory copper melting furnace,almost the same leaching trends were shown on Cu,Zn,Al,and Si under the strains ACTT23270 and TM-32 uses.     

Simultaneous removal of ammonium and phosphate by zeolite synthesized from coal fly ash as influenced by acid treatment

Zeolite synthesized from fly ash （ZFA） without modification is not efficient for the purification of NH4＋ and phosphate at low concentrations that occur in real effluents, despite the high potential removal capacity. To develop an effective technique to enhance the removal efficiency of ammonium and phosphate at low concentrations, ZFA was modified with acid treatment and the simultaneous removal of ammonium and phosphate in a wide range of concentration was investigated. It was seen that when compared with untreated ZFA, only the treatment by 0.01 mol/L of H2SO4 significantly improved the removal efficiency of ammonium at low initial concentrations. The behavior was well explained by the pH effect. Treatment by more concentrated H2SO4 led to the deterioration of the ZFA structure and a decrease in the cation exchange capacity. Treatment by 0.01 mol/L H2SO4 improved the removal efficiency of phosphate by ZFA at all initial P concentrations, while the treatment by concentrated H2SO4 （≥0.9 mol/L） resulted in a limited maximum phosphate immobilization capacity （PIC）. It was concluded that through a previous mild acid treatment （e.g. 0.01 mol/L of H2SO4）, ZFA can be used in the simultaneous removal of NH4＋ and P at low concentrations simulating real effluent.