基于Landsat8影像估算新安江水库光合有效辐射漫射衰减系数

光合有效辐射(photosynthetically active radiation,PAR)是指可以被植物利用并进行光合作用的那部分太阳辐射,其进入湖水后受光学组分(悬浮颗粒、有色可溶性有机物和浮游植物)的吸收和散射作用发生衰减,对湖泊生物的密度和分布具有重要影响.本研究构建了基于Landsat 8影像数据的较为清洁的新安江水库PAR漫衰减系数的遥感估算模型,进而分析其时空分布特征及主要影响因素.结果表明,利用Landsat 8的第二、三和第八波段构建的多元回归模型能够得到较为准确的估算结果,模型决定系数为0.87.利用独立样本对构建的模型验证,预测值和实测值相对误差绝对值均值为9.16%,均方根误差为0.06 m~(-1),由此可见利用Landsat 8数据的3个波段,采用多元回归模型能够较好地估算较清洁水体的PAR漫射衰减系数.基于14景Landsat 8影像发现,新安江水库PAR漫射衰减系数季节差异性明显,秋季(9~11月)和夏季(6~8月)PAR漫射衰减系数较高,分别为(0.82±0.60)m~(-1)和(0.77±0.41)m~(-1),而冬季(12~次年2月)和春季(3~5月)PAR漫射衰减系数相对较低,分别为(0.56±0.50)m~(-1)和(0.40±0.45)m~(-1).新安江水库PAR漫射衰减系数空间差异性显著,全湖PAR漫射衰减系数变化范围为(0.002~13.86)m~(-1),均值为(0.64±0.49)m~(-1).漫射衰减系数的季节变化主要是由季节性降雨和浮游植物季节性生长引起,空间差异性主要由外源河流输入和部分水域采砂过程导致悬浮物浓度变化引起.     

巢湖水体漫衰减系数特性及其影响因子分析

根据2009年6月巢湖32个样点的实测数据,分析巢湖水体各组分的吸收、后向散射特性以及水体漫衰减系数光谱特征,并通过Lee模型计算各影响因子对漫衰减系数的贡献率,在此基础上,进一步探讨巢湖水体漫衰减系数与各衰减因子浓度的关系.结果表明,非色素颗粒物、有色可溶性有机物(CDOM)吸收均随着波段增加呈现不断衰减趋势,400...     

北天堂垃圾污染场地氧化还原分带及污染物自然衰减研究

通过对北京市北天堂垃圾填埋场周围实际监测数据资料的分析,研究了垃圾填埋污染场地的氧化还原分带和污染物的自然衰减作用.结果表明,北天堂垃圾填埋污染场地存在氧化还原分带现象,依据各氧化还原带标志性物质浓度的分布规律和特点划分了5个氧化还原带,即产甲烷带、硫酸盐还原带、铁还原带、硝酸盐还原带和氧还原带.不同有机污染物在不同的氧化还原带中的衰减不同;挥发酚和氰化物在硫酸盐还原带中的含量相对较高,分别为0.005和0.019 μg/L;Cr、Pb、Ni、As、Cu、Cd、Zn和Mn等重金属在产甲烷带中的含量相对较高,分别为25.11、 33.82、 29.93、 3.18、 2.3、 0.1、 283.1、 1 220　μg/L.因此,氧化还原带对污染物的衰减起重要作用.     

浅水湖泊水动力过程对藻型湖区水体生物光学特性的影响

基于2010年7月底至8月初对太湖藻型湖区梅梁湾沿岸带水域不同风速条件下水下光场的原位连续高频观测,通过对水下辐照度、光束衰减系数、吸收系数、相关理化参数及气象水文参数的测定与分析,揭示了该区域水体的生物光学特性变化及其与水动力过程的关系.结果表明,总颗粒物吸收系数ap(440)、非色素颗粒物吸收系数ad(440)、浮游植物吸收系数aph(440)及有色可溶性有机物吸收系数aCDOM(440)在小风(30 min内平均风速<3 m.s-1)、中风(3 m.s-1<风速<5 m.s-1)和大风(风速>5 m.s-1)作用下分别为3.97、3.97、6.58 m-1;1.69、2.17、4.20 m-1;2.28、1.80、1.33 m-1;1.05、1.04、1.08 m-1,其中变幅最大的为非色素颗粒物,CDOM吸收系数在不同风速条件下差别不大.水体各组分在PAR波段积分值的贡献率的变化规律为:小风速下浮游植物吸收系数的贡献最大(达42.5%),随着风速的增大,CDOM、浮游植物、纯水吸收系数的贡献率均有降低的趋势,而非色素颗粒物的贡献率则显著增大,分别为33.0%、41.7%、52.0%.PAR漫射衰减系数与10min平均风速呈显著线性相关,风速引起的沉积物再悬浮对PAR漫射衰减系数的影响显著,从小风到大风,PAR漫射衰减系数增加了80.0%,对应真光层深度降低了42.2%.PAR漫射衰减系数、750 nm波长处的光束衰减系数、总悬浮物浓度与风速、波高、波切应力均存在显著正相关,其中又以PAR漫射衰减系数的相关性最为显著.高频观测结果揭示了浅水湖泊藻型湖区水动力过程通过引起沉积物再悬浮、浮游植物的混合及迁移显著改变水体生物光学特性短期变化.     

Correlation of Black Smoke and Nitrogen Oxides Emissions Through Field Testing of in-Use Diesel Vehicles

The U.S. Environmental Protection Agency Environmental Monitoring and Assessment Program (EMAP) uses water clarity as a water quality indicator for integrated assessments of coastal waters. After the publication of the first National Coastal Condition Report (USEPA, 2001c), the national water clarity reference value of 10% of ambient surface light at 1~m depth was reevaluated and modified to reflect expected differences in regional reference light conditions. These regional differences range from naturally turbid estuaries like those found in Mississippi and Louisiana to clear water estuaries expected to support extensive beds of submerged aquatic vegetation in, e.g., Florida and Tampa Bays. For the second National Coastal Condition Report, water clarity was assessed based on regional reference values (USEPA, 2004). Different regional water clarity reference values and data collection methods necessitated the development of a water clarity index based on light attenuation coefficients (k). This index incorporates regional reference conditions and is interchangeable with secchi depth and percent light transmission calculated from light meter measurements. Evaluation of the water clarity index shows that k values based on transmissivity at 1~m can be estimated from secchi depth measurements and successfully used as a surrogate for transmissivity calculated from light meter data. An approach for assessing water clarity in Gulf of Mexico estuaries using light meter data and secchi depth is presented.     

Aerobic biodegradation of vinyl chloride and cis-1,2-dichloroethylene in aquifer sediments

Laboratory batch experiments have been performed with sediment and groundwater obtained from two sites in Denmark to study the aerobic biodegradation of vinyl chloride (VC) and cis-1,2-dichloroethylene (c-1,2-DCE) to assess the natural aerobic biodegradation potential at two sites. The experiments revealed that VC was degraded to below the detection limit within 204 and 57 days at the two sites. c-1,2-DCE was also degraded in the experiments but not completely. At the two sites 50% and 35% was removed by the end of the experimental period of 204 and 274 days. The removal of c-1,2-DCE seems to occur concomitantly with VC indicating that the biodegradation of c-1,2-DCE may depend on the biodegradation of VC. However, in both cases natural groundwater was mixed with sediment and consequently there may be other compounds (e.g. ammonium, natural organic compound etc.) that serves as primary substrates for the co-metabolic biodegradation of c-1,2-DCE. At one of the sites methane was supplied to try to enhance the biodegradation of VC and c-1,2-DCE. That was successful since the time for complete biodegradation of VC decreased from 204 days in the absence of methane to 84 days in the presence of methane. For c-1,2-DCE the amount that was biodegraded after 204 days increased from 50% to 90% as a result of the addition of methane. It seems like a potential for natural biodegradation exists at least for VC at these two sites and also to some degree for c-1,2-DCE.     

Occurrence and attenuation of specific organic compounds in the groundwater plume at a former gasworks site

The changing contaminant pattern with travelled distance was investigated in the anaerobic groundwater plume downstream from an extended zone containing residual NAPL at a former gas manufacturing plant. With increasing distance, O- and N-heterocyclic aromatic compounds are enriched in the plume relative to the usually assessed coal tar constituents (poly- and monocyclic aromatic compounds). In a first approximation, the overall concentration decrease of the investigated compounds follows a first order overall decay. The half life distance in the plume downgradient from the source varied between 20 m for benzene and up to 167-303 m for alkyl-naphthalenes. Acenaphthene is degraded only within about 50 m downstream from the source area, then its concentration remains constant (ca. 180 microg/l) and far above the legal limit. Dimethyl-benzofurans were the most recalcitrant among all compounds which could be quantified with the analytical method available. The overall groundwater contamination in the plume is seriously underestimated if only BTEX and 16-EPA-PAHs are monitored.     

Natural attenuation/phytoremediation in the vadose zone of a former industrial sludge basin

The natural attenuation of polyaromatic hydrocarbons (PAHs) in the vadose zone of a naturally revegetated former industrial sludge basin (0.45 ha) was examined. This was accomplished by comparing the concentration of 16 PAH contaminants present in sludge collected below the root zone of plants with contaminants present at 3 shallower depths within the root zone. Chemical analysis of 240 samples from 60 cores showed the average concentration of total and individual PAHs in the 0-30 cm, 30-60 cm, and bottom of the root zone strata were approximately 10, 20, and 50%, respectively, of the 16, 800 ppm average total PAH concentration in deep non-rooted sludge. Statistically significant differences in average PAH concentrations were observed between each strata studied and the non-rooted sludge except for the concentrations of acenaphthene and chrysene present at the bottom of the root zone in comparison to sludge values. The rooting depth of the vegetation growing in the basin was dependent on both vegetation type and plant age. Average rooting depths for trees, forbs (herbaceous non-grasses), and grasses were 90, 60, and 50 cm, respectively. The deepest root systems observed (100-120 cm) were associated with the oldest (12-14 year-old) mulberry trees. Examination of root systems and PAH concentrations at numerous locations and depths within the basin indicated that plant roots and their microbially active rhizospheres fostered PAH disappearance; including water insoluble, low volatility compounds, i.e. benzo(a)pyrene and benzo(ghi)perylene. The reduced concentration of PAHs in the upper strata of this revegetated former sludge basin indicated that natural attenuation had occurred. This observation supports the concept that through appropriate planting and management practices (phytoremediation) it will be possible to accelerate, maximize, and sustain natural processes, whereby even the most recalcitrant PAH contaminants (i.e. benzo(a)pyrene) can be remediated over time.     

Dendroremediation of trinitrotoluene (TNT) part 1: Literature overview and research concept

BACKGROUND, AIM AND SCOPE: For decades, very large areas of former military sites have been contaminated diffusely with the persistent nitroaromatic explosive 2,4,6-trinitrotoluene (TNT). The recalcitrance of the environmental hazard TNT is to a great extent due to its particulate soil existence, which leads to slow but continuous leaching processes. Although improper handling during the manufacture of TNT seems to be a problem of the past in developed countries, environmental deposition of TNT and other explosives is still going on unfortunately, resulting from thousands of unexploded ordnance or low order explosions at munitions test areas and at current battlefields. OBJECTIVE: Sustainable phytoremediation strategies for explosives in Germany, which intend to use trees to decontaminate soil and groundwater ('dendroremediation'), have to consider that most of the former German military sites are already covered with woodlands, mainly with conifer stands. Therefore, parallel investigation of the remediation potential is necessary for both of the selected hybrids of fast growing broadleaf trees, which are waiting for planting and forest conifers, which have already proven for decades that they are able to grow on explosive contaminated sites. MAIN FEATURES: A short literature review is given regarding phytoremediation of TNT with herbaceous plants and some general aspects of dendroremediation are discussed. Furthermore, an overview of our TNT-dendroremediation research network is introduced, which has the strategic goal to make dendroremediation more calculable for a series of potent trees for site-adapted in situ application and for the assessment of tree remediation potentials in natural attenuation processes. RESULTS AND DISCUSSION: Some of our methods, results and conclusions yet unpublished are presented. For a preliminary calculation of area-related annual TNT dendroremediation potential of five-year-old trees, the following values were assessed: Salix EW-13 6.0, Salix EW-20 8.5, Populus ZP-007 4.2, Betula pendula 5.2, Picea abies 1.9 and Pinus sylvestris 0.8 g m(-2) a(-1). For a 45-year-old spruce forest, an annual natural attenuation potential of 4.2 g TNT m(-2) a(-1) was found. CONCLUSION, RECOMMENDATIONS AND PERSPECTIVE: Our main results deliver quantitative proposals for dendroremediation strategies in situ and provide decision aids. Also aspects of growth of raw materials for energy production are considered. Our dendroremediation research concept for TNT and its congeners can be easily completed for other trees of interest and it can also be applied to herbaceous plants. Knowing the current bottlenecks of phytoremediation and considering the known environmental behaviour of other contaminants, elements of our methodological approach may be easily adapted to those pollutant groups, e.g. for pesticides, pharmaceuticals, PAHs, chlorinated recalcitrants and, with some restrictions, to inorganics and to multiple contaminations. Our dynamical dendrotolerance test systems will help to predict tree growth on polluted areas. To provide some light into the black box of TNT dendroremediation, experimental data regarding the uptake, distribution and degradation of [14C]-TNT in mature tree tissues will be reported in the second part of this publication.     

Modelling of iron cycling and its impact on the electron balance at a petroleum hydrocarbon contaminated site in Hnevice, Czech Republic

Over a period of several decades multiple leaks of large volumes from storage facilities located near Hnevice (Czech Republic) have caused the underlying Quaternary aquifer to be severely contaminated with nonaqueous phase liquid (NAPL) petroleum hydrocarbons. Beginning in the late 1980's the NAPL plume started to shrink as a consequence of NAPL dissolution exceeding replenishment and due to active remediation. The subsurface was classified geochemically into four different zones, (i) a contaminant-free zone never occupied by NAPL or dissolved contaminants, (ii) a re-oxidation zone formerly occupied by NAPL, (iii) a zone currently occupied by NAPL, and (iv) a lower fringe zone between the overlying NAPL and the deeper underlying contaminant-free zone. The study investigated the spatial and temporal variability of the redox zonation at the Hnevice site and quantified the influence of iron-cycling on the overall electron balance. As a first step inverse geochemical modelling was carried out to identify possible reaction models and mass transfer processes. In a subsequent step, two-dimensional (forward) multi-component reactive transport modelling was performed to evaluate and quantify the major processes that control the geochemical evolution at the site. The study explains the observed enrichment of the lower fringe zone with ferrihydrite as a result of the re-oxidation of ferrous iron. It suggests that once the NAPL zone started to shrink the dissolution of previously formed siderite and FeS by oxygen and nitrate consumed a significant part of the oxidation capacity for a considerable time period and therefore limited the penetration of electron acceptors into the NAPL contaminated zone.