福建近岸海域悬浮泥沙浓度遥感定量监测研究

论文在分析MODIS数据对海洋水体反射光谱特征的基础上,选用合适的探测波段构成悬浮泥沙遥感参数,并根据2003~2004年福建近岸海域海洋监控区内9个站点的海洋水色数据建立悬浮泥沙浓度遥感定量反演模式。利用已建立的模式对2001~2005年福建近岸海域悬浮泥沙浓度进行遥感反演,根据反演结果分析该海域悬浮泥沙浓度的分布及其变化特征,着重分析闽江口海域的悬浮泥沙运动特点。结果表明:福建近岸海域悬浮泥沙浓度与基于MODIS蓝光(0.438~0.448μm)和绿光(0.545~0.565μm)探测波段数据构成的遥感参数呈指数函数关系,定量反演效果比较理想,反演结果能客观地揭示福建近岸海域悬浮泥沙的浓度分布及其变化特征,为今后对该海域悬浮泥沙运动规律的深化研究奠定了基础。     

多尺度PM_(2.5)分布特征的空间插值与遥感反演对比

精确识别污染物浓度的空间分布是进行区域大气污染防治的重要基础。利用MODIS卫星数据,采用基于地面气象和环境空气质量监测站点观测数据为基础的反演模型,反演获取2013年12月珠三角地区典型大气污染过程1 km分辨率的PM_(2.5)浓度数据,对比分析遥感反演及基于环境空气质量监测站点观测数据的空间插值方法对区域、城市和乡镇尺度PM_(2.5)浓度空间分布特征的再现效果差异。结果表明,珠三角地区PM_(2.5)遥感反演结果与地面观测数据的相关性达到0.74,相关性水平较好,遥感反演结果可描述区域、城市和乡镇尺度上PM_(2.5)污染浓度的空间分布特征,识别不同空间位置的污染程度差异;基于站点观测数据的空间插值方法对PM_(2.5)浓度空间分布特征的再现能力有限,在区域尺度PM_(2.5)浓度空间分布特征分析时效果尚可,在站点有限的城市和乡镇尺度分析中效果不佳,容易产生对高浓度污染地区的误判;在需要利用站点观测数据分析区域尺度PM_(2.5)浓度空间分布特征时,析取克里金、反距离权重或径向基函数插值方法的效果相对较好。     

太湖水域叶绿素a浓度的遥感反演研究

利用太湖水域MODIS遥感数据的各波段反射率组合计算值,与实测的叶绿素a浓度进行相关性分析,找到相关性最好的反射率组合,建立反演太湖叶绿素a浓度的遥感模型.结果表明,利用MODIS数据可以较好地实现对太湖水域叶绿素a浓度的定量反演计算,并以MODIS数据第3、第17波段的反射率组合作为遥感指数建立了反演叶绿素a浓度的模型.第3、第17波段的波长范围分别为459nm～479nm、890nm～920nm,这一波段选择与以往使用TM数据得到的结论有所不同.     

基于集合均方根滤波的太湖叶绿素a浓度估算与预测

叶绿素a浓度作为表征水质状况的重要参数之一,反映了水体富营养化程度和藻类含量,是决定水体的反射光谱特征的重要因素,也是水质遥感领域研究较多的一项水质参数.研究叶绿素a浓度的遥感定量反演可以为湖泊水质监测与评价提供新的思路和方法.本研究发展了一个基于集合均方根滤波和风生流的污染物扩散模型的数据同化方案,并结合2010年5月20日的太湖3个浮标观测站点的观测数据进行了同化实验.首先对太湖叶绿素a浓度进行同化估算,然后利用优化后的估算结果对太湖叶绿素a浓度进行了为期6 h的预报.在同化阶段,均方根误差分别从1.58、1.025、2.76降低到了0.465、0.276、1.01,平均相对误差也从0.2降低到了0.05、0.046、0.069.在预报阶段,均方根误差从1.486、1.143、2.38降低到了0.017、0.147、0.23,平均相对误差也从0.2降低到了0.002、0.025、0.019.结果表明,利用集合均方根滤波的数据同化方法可以有效地提高太湖叶绿素a浓度的估算与预报精度.     

面向GF-1WFV数据的闽江下游叶绿素a反演模型研究

叶绿素a浓度是可直接遥感反演的重要水质参数之一,常用来评价水体的富营养化程度.为建立适合于闽江下游叶绿素a浓度的反演模型,利用地面采样数据,结合GF-1 WFV光谱响应函数,选用多元回归、BP神经网络和随机森林方法,构建了叶绿素a浓度反演模型;并根据验证数据与实测值之间的决定系数(R~2)、均方根误差(RMSE)和平均相对误差对模型反演结果进行了比较.结果发现,随机森林模型的R~2为0.895,RMSE为1.994 mg·m~(-3),平均相对误差为11.502%,是3种模型中最优的.为了评估模型的性能,进一步比较了WFV影像像元反射率反演的叶绿素a浓度值与相应的实测值.结果表明,随机森林模型同样具有较高的精度,其R~2为0.709,RMSE为3.540 mg·m~(-3),平均相对误差为25.616%.本研究可为闽江下游水环境的监测提供一定的理论依据和技术参考.     

基于环境一号卫星数据的太湖叶绿素a浓度反演

环境一号卫星在大型水体水环境监测与评价中具有独特的优势。为探求遥感影像在水体叶绿素a浓度反演中的应用,基于环境一号卫星CCD数据和同步实测叶绿素a浓度值,通过影像辐射定标、大气校正和几何精校正等预处理获取水体反射率,分别将单波段和不同特征波段组合的反射率与实测叶绿素a值进行皮尔逊相关分析,选取R20.8的波段组合进行建模,通过对3种波段组合反演结果对比和精度验证,发现基于CCD数据第4波段与第3波段反射率比值的二次模型具有良好的反演效果,模型预测值与实测值的最小相对误差为0.76%,平均相对误差10.99%,均方根误差为0.007 6 mg/L,明显低于实测叶绿素a浓度的平均值;最后基于该模型实现了太湖叶绿素a浓度反演,并对叶绿素a的时空分布进行了初步分析。     

利用高光谱反演模型评估太湖水体叶绿素a浓度分布

叶绿素a浓度是评价水体富营养化和初级生产力的一个重要参数,高光谱遥感是获取叶绿素a浓度的有效手段.为建立太湖水域叶绿素a的最佳高光谱估算模型,选取2015年5—7月共计60组同步实测高光谱数据和叶绿素a浓度数据,在地面光谱反射率和叶绿素a浓度相关性分析的基础上,使用2∶1的数据样本进行太湖水域叶绿素a的最佳高光谱估算模型的建立和验证,筛选模型分别为波段比值、三波段、荧光峰位置、峰谷距离、一阶微分、NDCI(Normalized Difference Chlorophyll Index)、峰面积、荧光峰高度、WCI(Water Chlorophyll-a Index)和四波段模型.结果表明,建模得到的四波段模型决定系数最高,峰面积模型的决定系数相对最低;四波段模型的反演精度最高,均方根误差(RMSE)为0.00376 mg·L~(-1),平均绝对误差(MAPE)为27.86%,而WCI模型的反演精度相对最低,RMSE为0.01231 mg·L~(-1),MAPE为45.11%.将反演精度最高的四波段模型应用于2015年8月3日的两景HSI(Hyperspectral Imaging Radiometer)高光谱影像数据,也得到较高精度,利用同步实测叶绿素a浓度验证的决定系数为0.7643,RMSE为0.00433 mg·L~(-1),MAPE为45.62%.在春、夏季叶绿素对水体光学特性占主导作用且叶绿素分布均匀的情景下,本研究可为太湖水域叶绿素a的高光谱反演和水环境监测提供有价值的参考,其它季节水体光谱特点的研究尚待进一步开展.     

辽东湾MODIS生物光学算法研究(Ⅰ)算法适用性评估

辽东湾是典型的复杂二类水体,我们利用2002～2004年在辽东湾现场实测的叶绿素a数据(分光法、荧光法和HPLC法),以及水面之上法现场实测的离水辐射率和遥感反射率数据模拟的MODIS各相应波段值对MODIS海洋水色算法进行了评估.评估的MODIS生物光学算法有四个,即CZCS_pigm、chlor_MODIS、chlor_a_2和chlor_a_3算法.结果表明,两个一类水体生物光学算法(CZCS_pigm和chlor_MODIS)反演值与分光法和荧光法测试分析结果相比,算法均低估了叶绿素a浓度,与HPLC分析结果相比算法高估了叶绿素a浓度;两个二类水体算法(chlor_a_2和chlor_a_3)与所有叶绿素a分析方法相比,均高估了叶绿素a浓度.根据MODIS生物光学算法在辽东湾的具体表现,我们认为HPLC法分析的叶绿素a浓度更适合于作为海洋水色算法评估的现场检验依据.叶绿素a浓度的反演值和实测值之间较低的相关系数则显示MODIS两个一类水体算法所采用的波段比值不适合本海区.     

基于OLCI数据的福建近海悬浮物浓度遥感反演

悬浮物（TSM）是评估水质的重要指标,也是水色遥感反演的核心参数之一.海陆色度仪（OLCI）是新一代海洋水色传感器,具有良好的光谱及时空分辨率.为有效监测福建近海悬浮物浓度的时空变化,本文结合OLCI遥感数据和现场实测悬浮物浓度数据,使用CatBoost、随机森林和多元回归方法,分别构建悬浮物浓度反演模型,最后使用验证集对比分析不同模型的反演精度.结果表明,CatBoost模型估算精度最高,均方根误差（RMSE）为2.76 mg·L^-1,平均绝对百分比误差（MAPE）为23.67%,决定系数R²为0.89.使用CatBoost模型对2017—2018年多时相OLCI影像进行TSM浓度遥感反演,结果发现,福建近海TSM浓度变化显著,但总体呈现近岸高于远岸、北部高于南部、江河入海口和港湾处高于周围其他海域、春季高于夏季的时空分布特征.本研究可为福建近海的悬浮物浓度监测提供一种有效的方法,也进一步证明了OLCI影像良好的水色反演能力,可作为水质监测的有效遥感数据源.     

基于TM数据北京城区水体叶绿素a浓度反演方法研究

叶绿素是城市水体富营养化的重要表征参数.以北京城区重点水体为研究对象,利用2011年6月8日TM遥感影像及同步获取的实测数据,在对TM数据进行几何校正和大气校正等预处理的基础上,选取相关性最大的TM2/(TM1 +TM4)波段组合进行叶绿素a浓度反演;利用2008 ～ 2010年的历史TM影像及人工水质站点准同步的实测数据,对模型的精度及适用性进行分析得出:回归模型适用于30 m以上的北京城区水体叶绿素a浓度监测,相对误差为17.04％.     

Toxic effects of acetochlor, methamidophos and their combination on nifH gene in soil

Toxic effects of two agrochemicals on nifH gene in agricultural black soil were investigated using denaturing gradient gel electrophoresis （DGGE） and sequencing approaches in a microcosm experiment. Changes of soil nifH gene diversity and composition were examined following the application of acetochlor, methamidophos and their combination. Acetochlor reduced the nifH gene diversity （both in gene richness and diversity index values） and caused changes in the nifH gene composition. The effects of acetochlor on nifH gene were strengthened as the concentration of acetochlor increased. Cluster analysis of DGGE banding patterns showed that nifH gene composition which had been affected by low concentration of acetochlor （50 mg/kg） recovered firstly. Methamidophos reduced nifH gene richness that except at 4 weeks. The medium concentration of methamidophos （150 mg/kg） caused the most apparent changes in nifH gene diversity at the first week while the high concentration of methamidophos （250 mg/kg） produced prominent effects on nifH gene diversity in the following weeks. Cluster analysis showed that minimal changes of nifH gene composition were found at 1 week and maximal changes at 4 weeks. Toxic effects of acetochlor and methamidophos combination on nifH gene were also apparent. Different nifH genes （bands） responded differently to the impact of agrochemicals： four individual bands were eliminated by the application of the agrochemicals, five bands became predominant by the stimulation of the agrochemicals, and four bands showed strong resistance to the influence of the agrochemicals. Fifteen prominent bands were partially sequenced, yielding 15 different nifH sequences, which were used for phylogenetic reconstructions. All sequences were affiliated with the alpha- and beta-proteobacteria, showing higher similarity to eight different diazotrophic genera.     

Arsenic uptake by arbuscular mycorrhizal maize （Zea mays L.） grown in an arsenic-contaminated soil with added phosphorus

The effects of arbuscular mycorrhizal (AM) fungus (Glomus mosseae) and phosphorus (P) addition (100 mg/kg soil) on arsenic (As) uptake by maize plants (Zea mays L.) from an As-contaminated soil were examined in a glasshouse experiment.Non-mycorrhizal and zero-P addition controls were included.Plant biomass and concentrations and uptake of As,P,and other nutrients,AM colonization,root lengths,and hyphal length densities were determined.The results indicated that addition of P significantly inhibited root colonization and development of extraradical mycelium.Root length and dry weight both increased markedly with mycorrhizal colonization under the zero-P treatments,but shoot and root biomass of AM plants was depressed by P application.AM fungal inoculation decreased shoot As concentrations when no P was added,and shoot and root As concentrations of AM plants increased 2.6 and 1.4 times with P addition,respectively.Shoot and root uptake of P,Mn,Cu,and Zn increased,but shoot Fe uptake decreased by 44.6%,with inoculation, when P was added.P addition reduced shoot P,Fe,Mn,Cu,and Zn uptake of AM plants,but increased root Fe and Mn uptake of the nonmycorrhizal ones.AM colonization therefore appeared to enhance plant tolerance to As in low P soil,and have some potential for the phytostabilization of As-contaminated soil,however,P application may introduce additional environmental risk by increasing soil As mobility.     

Degradation of metabolites accumulated of benzo[a]pyrene by coupling Penicillium Chrysogenum with KMnO4

Several main metabolites of benzo[a]pyrene （BaP） formed by Penicillium chrysogenum, Benzo[a]pyrene-1,6-quinone （BP 1,6- quinone）, trans-7,8-dihydroxy-7,8-dihydrobenzo[a]pyrene （BP 7,8-diol）, 3-hydroxybenzo[a]pyrene （3-OHBP）, were identified by high-performance liquid chromatography （HPLC）. The three metabolites were liable to be accumulated and were hardly further metabolized because of their toxicity to microorganisms. However, their further degradation was essential for the complete degradation of BaP. To enhance their degradation, two methods, degradation by coupling Penicillium chrysogenum with KMnO4 and degradation only by Penicillium chrysogenum, were compared; Meanwhile, the parameters of degradation in the superior method were optimized. The results showed that （1） the method of coupling Penicillium chrysogenum with KMnO4 was better and was the first method to be used in the degradation of BaP and its metabolites; （2） the metabolite, BP 1,6-quinone was the most liable to be accumulated in pure cultures; （3） the effect of degradation was the best when the concentration of KMnO4 in the cultures was 0.01% （w/v）, concentration of the three compounds was 5 mg/L and pH was 6.2. Based on the experimental results, a novel concept with regard to the bioremediation of BaP-contaminated environment was discussed, considering the influence on environmental toxicity of the accumulated metabolites.     

Impact of atrazine and nitrogen fertilizers on the sorption of chlorotoluron in soil and model sorbents

Sorption of chlorotoluron in ammonium sulfate, urea and atrazine multi-solutes system was investigated by batch experiments. The results showed application of nitrogen fertilizers to the soil could affect the behavior of chlorotoluron. At the same concentration of N, sorption of chlorotoluron decreased as the concentration of atrazine increased on the day 0 and 6 in soil, respectively. The sorption of chlorotoluron increased from 0 to 6 d when soils were preincubated with deionized water, ammonium sulfate and urea solution for 6 d. That indicated incubation time was one of the most important factors for the sorption of chlorotoluron in nitrogen fertilizers treatments. The individual sorption isotherms of chlorotoluron in rubbery polymer and silica were strictly linear in single solute system, but there were competition sorption between pesticides or between pesticides and nitrogen fertilizers. That indicated the sorption taken place by concurrent solid-phase dissolution mechanism and sorption on the interface of water-organic matter or water-mineral matter.     

Potential of plant polyphenol oxidases in the decolorization and removal of textile and non-textile dyes

In this study an effort has been made to use plant polyphenol oxidases; potato （Solanum tuberosum） and brinjal （Solanum melongena）, for the treatment of various important dyes used in textile and other industries. The ammonium sulphate fractionated enzyme preparations were used to treat a number of dyes under various experimental conditions. Majority of the treated dyes were maximally decolorized at pH 3.0. Some of the dyes were quickly decolorized whereas others were marginally decolorized. The initial first hour was sufficient for the maximum decolorization of dyes. The rate of decolorization was quite slow on long treatment of dyes. Enhancement in the dye decolorization was noticed on increasing the concentration of enzymes. The complex mixtures of dyes were treated with both preparations of polyphenol oxidases in the buffers of varying pH values. Potato polyphenol oxidase was significantly more effective in decolorizing the dyes to higher extent as compared to the enzyme obtained from brinjal polyphenol oxidase. Decolorization of dyes and their mixtures, followed by the formation of an insoluble precipitate, which could be easily removed simply by centrifugation.     

Removal of heavy metals from sewage sludge by low costing chemical method and recycling in agriculture

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Single and joint effects of pesticides and mercury on soil urease

The influence of two pesticides including chlorimuron-ethyl and furadan and mercury （Hg） on urease activity in 4 soils （meadow burozem and phaeozem） was investigated. The soils were exposed to various concentrations of the two pesticides and Hg individually and simultaneously. Results showed that there was a close relationship between urease activity and organic matter content in soil. Chlorimuron-ethyl and furadan could both activate urease in the 4 soils. The maximum increment of urease activity by chlorimuronethyl was up to 14%-18%. There was almost an equal increase （up to 13%-21%） in the urease activity by furadan. On the contrary, Hg markedly inhibited soil urease activity. A logarithmic equation was used to describe the relationship （P〈0.05） between the concentration of Hg and the activity of soil urease in the 4 tested soils. Semi-effect dose （ED50） values by the stress of Hg based on the inhibition of soil urease in the 4 soils were 88, 5.5, 24 and 20 mg/kg, respectively, according to the calculation of the corresponding equations. The interactive effect of chlorimuron-ethyl or furadan with metal Hg on soil urease was mainly synergic at the highest tested concentrations.     

Isolation and preliminary characterization of a 3-chlorobenzoate degrading bacteria

A study was conducted to compare the diversity of 2-, 3-, and 4-chlorobenzoate degraders in two pristine soils and one contaminated sewage sludge. These samples contained strikingly different populations of mono-chlorobenzoate degraders. Although fewer cultures were isolated in the uncontaminated soils than contaminated one, the ability of microbial populations to mineralize chlorobenzoate was widespread. The 3- and 4-chlorobenzoate degraders were more diverse than the 2-chlorobenzoate degraders. One of the strains isolated from the sewage sludge was obtained. Based on its phenotype, chemotaxonomic properties and 16S rRNA gene, the organism S-7 was classified as Rhodococcus erythropolis. The strain can grow at temperature from 4 to 37℃. It can utilize several （halo）aromatic compounds. Moreover, strain S-7 can grow and use 3-chlorobenzoate as sole carbon source in a temperatures range of 10-30℃ with stoichiometric release of chloride ions. The psychrotolerant ability was significant for bioremediation in low temperature regions. Catechol and chlorocatechol 1,2-dioxygenase activities were present in cell free extracts of the strain, but no （chloro）catechol 2,3- dioxygenase activities was detected. Spectral conversion assays with extracts from R. erythropolis S-7 showed accumulation of a compound with a similar UV spectrum as chloro-cis,cis-muconate from 3-chlorobenzoate. On the basis of these results, we proposed that S-7 degraded 3-chlorobenzoate through the modified ortho-cleave pathway.     

Organochlorine pesticides in soils under different land usage in the Taihu Lake region, China

A field study was conducted in the Taihu Lake region, China in 2004 to reveal the organochlorine pesticide concentrations in soils after the ban of these substances in the year 1983. Thirteen organochlorine pesticides (OCPs) were analyzed in soils from paddy field, tree land and fallow land. Total organochlorine pesticide residues were higher in agricultural soils than in uncultivated fallow land soils. Among all the pesticides, ΣDDX (DDD, DDE and DDT) had the highest concentration for all the soil samples, ranging from 3.10 ng/g to 166.55 ng/g with a mean value of 57.04 ng/g and followed by ΣHCH, ranging from 0.73 ng/g to 60.97 ng/g with a mean value of 24.06 ng/g. Dieldrin, endrin, HCB and α-endosulfan were also found in soils with less than 15 ng/g. Ratios of p,p'-(DDD DDE)/DDT in soils under three land usages were: paddy field ＞ tree land ＞ fallow land, indicating that land usage inlfuenced the degradation of DDT in soils. Ratios of p,p'-(DDD DDE)/DDT ＞1, showing aged residues of DDTs in soils of the Taihu Lake region. The results were discussed with data from a former study that showed very low actual concentrations of HCH and DDT in soils in the Taihu Lake region, but according to the chemical half-lives and their concentrations in soils in 1980s, the concentration of DDT in soils seemed to be underestimated. In any case our data show that the ban on the use of HCH and DDT resulted in a tremendous reduction of these pesticide residues in soils, but there are still high amounts of pesticide residues in soils, which need more remediation processes.     

Sorption of 1-naphthol by plant cuticular fractions

The contribution of aliphatic-rich plant biopolymer to sorption of hydrophobic organic compounds is significantly important because of their preservation and accumulation in the soil environment,but sorption mechanism is still not fully understood.In this study, sorption of 1-naphthol by plant cuticular fractions was examined to better understand the contributions of respective fraction.Toward this end,cuticular materials were isolated from the fruits of tomato by chemical method.The tomato cuticle sheet consisted of waxes (6.5 wt%),cuticular monomer (69.5 wt%),and polysaccharide (24.0 wt%).Isotherms of l-naphthol to the cuticular fractions were nonlinear (N value (0.82-0.90)) at the whole tested concentration ranges.The KodKow ratios for bulk cuticle (TC1),dewaxed cuticle (TC2),cutin (TC4),and desugared cuticle (TC5) were larger than unity,suggested that tomato bulk cuticle and cutin are much powerful solption medium.Sorption capability of cutin (TC4) was 2.4 times higher than the nonsaponifiable fraction (TC3).The 1-naphthol interactions with tomato cuticular materials were governed by both hydrophobic-type interactions and polar (H-bonding) interactions. Removal of the wax and polysaccharide materials from the bulk tomato cuticle caused a significant increase in the sorption ability of the cuticular material.There was a linear negative trend between K_(oc) values and the amount of polysaccharides or fraction's polarities ((N O)/C);while a linear positive relationship between K_(oc) values and the content of cutin monomer (linear R~2=0.993) was observed for present in the cuticular fractions.Predominant sorbent of the hydrophobic organic compounds (HOCs) in the plant cuticular fraction was the cutin monomer,contributing to 91.7% of the total sorption of tomato bulk cuticle.