治理后的太湖无锡区域底质中重金属污染现状及生态风险评价

以2005年以后太湖无锡区域底质为研究对象，分析了太湖底泥中重金属的含量分布及富集状况，采用地积累指数法和潜在生态危害指数法对重金属的生态危害进行评价。结果表明：太湖无锡区域底质受重金属轻度污染，含量高于全国水系沉积物平均值；地积累指数法显示太湖无锡区域底质中重金属污染排序为Cu=As〉Pb〉Zn〉Cr〉Cd〉Hg；金属对太湖无锡区域底质构成的潜在生态危害由强到弱为Hg〉Cu〉As〉Cd〉Pb〉Cr〉Zn；从区域上看，2种评价方法均表明底质中重金属危害程度为宜兴沿岸区〉梅梁湖〉五里湖〉贡湖无锡水域。     

Spatial Extent of Sediment Toxicity in U.S. Estuaries and Marine Bays

Acute, laboratory toxicity tests were performed by the National Oceanic and Atmospheric Administration (NOAA) on 1543 surficial sediment samples collected during 1991 through 1997 throughout 25 estuaries and marine bays. Selected areas were sampled along the Atlantic, Gulf of Mexico, and Pacific coasts. The toxicity of each sample was determined with 10-day amphipod survival tests performed with solid-phase (bulk) sediments. Collectively, the 1543 samples tested through 1997 represented a total area of approximately 7300 km². Toxicity was observed with the amphipod survival tests in samples that represented approximately 6% of the combined area. Using similar tests conducted on samples collected in different, but overlapping, study areas, the U.S. Environmental Protection Agency (EPA) estimated that approximately 7% of the combined estuarine area sampled was toxic. Generally, toxicity was most severe in northeastern and southwestern estuaries and least prevalent in southeastern and northwestern areas. However, considerable portions of the Pacific coast have not been tested with the same methods. In tests of CYP1A enzyme induction (n=464), samples were toxic that represented about 5% of the combined study areas. Toxicity was much more widespread, however, when the results of two sub-lethal tests were analyzed. Significant results occurred in samples that represented approximately 25% and 39% of the study areas in tests of sea urchin fertilization (n=1309) and microbial bioluminescence (n=1215), respectively.     

水石流概化水槽试验相似律的探讨

针对水石流粒粗，粘性小的特点，提出了利用水槽进行分段模拟水石流的设想，首次通过几何率解决难度较大的阻力相似问题，改变以往过度加糙的方式，通过变粒径尺度的方法消除了相模型沙级配不连续相似的问题，较好地实现了固体物质级配相停，达到了泥石流的密度相似和输沙相似，通过水槽概化模型实验实例，对本方法进行了验证。     

Water Quality and Metal Enrichment in Bed Sediments of the Rivers Kali and Hindon, India

Water-quality parameters and concentrations of various metals in bed sediments of the River Kali and the River Hindon in India were analysed to understand their behaviour in subtropical fluvial systems. Variations in the physico-chemical parameters of the river water and metal content in the bed sediments were recorded in four seasons of the year (post-monsoon, winter, summer and monsoon). Results show that water and sediments contain high cadmium (Cd) and Zinc (Zn). Total and soluble Cd and Zn profiles show that in summer, metals in the water phase exist predominantly in the bound form. Cd and Zn in bed sediments increase from the post-monsoon to the summer season. During and after the monsoon season, metal concentrations in sediments fall rapidly. Correlation coefficients of metals in sediments represent their common source and identical behaviour during transport.     

Determination of phenolic and steroid endocrine disrupting compounds in environmental matrices

BACKGROUND, AIM AND SCOPE: Many pollutants have received significant attention due to their potential estrogenic effect and are classified as endocrine disrupting compounds (EDCs). EDCs comprise many classes of organic compounds. The development or optimization of analytical protocols for the simultaneous determination of EDCs in environmental samples is an analytical challenge because these compounds exhibit different physicochemical characteristics, they occur in the aquatic environment in relatively low concentrations and, furthermore, environmental samples are considered as complex matrices. The aim of this study is the development of analytical methods for the simultaneous determination of phenolic and steroid EDCs in aqueous and solid samples. The target compounds are 4-nonylphenol, 4-octylphenol, their ethoxylate oligomers (mono- and di-ethoxylates of nonylphenol and octylphenol), bisphenol A, the estrogens (estriol, estrone, 17beta-estradiol, 17alpha-estradiol) and the synthetic steroids (mestranol and 17alpha-ethynylestradiol). MATERIALS AND METHODS: Solid phase extraction employing Oasis HLB cartridges and different elution solvents was used for the recovery studies of the target compounds from various types of water samples (ultrapure water, artificial seawater, river water and seawater). Ultrasonic assisted extraction was applied for the recovery of the target EDCs from the solid samples. The recoveries were assessed using various solvents for the extraction and the elution of EDCs from different SPE cartridges used for clean up. Gas chromatography-mass spectrometry after derivatization with N,O-bis(trimethylsilyl)-trifluoroacetamide was employed for the determination of these compounds. RESULTS AND DISCUSSION: The recovery rates of three elution solvents (methanol, acetone and ethylacetate) for the extraction of target EDCs from artificial seawater were assessed after preconcentration on SPE cartridges. Acetone showed better recoveries and was further tested for its extraction efficiency in different water types (river water, seawater). Ultrasonic assisted extraction was used for the recovery of target EDCs from solid matrices. Acetone, methanol, mixture of acetone-methanol (1:1) and ethylacetate were used as extraction solvents. Ethylacetate and the mixture of acetone-methanol (1:1) exhibited better extraction efficiencies. An additional clean up step was necessary for sediment samples. Different SPE cartridges were employed for clean up of the extracts (Oasis HLB, C18, Florisil, silica, combination of silica and alumina). Florisil cartridges were finally used. The proposed methods were further validated on the determination of target EDCs in field collected samples (river water, seawater, wastewater, total suspended solids and sediments) from the major area of Thessaloniki, Greece. CONCLUSIONS: Efficient and accurate integrated methods for the simultaneous determination of alkylphenols (nonylphenol, octylphenol), their ethoxylate oligomers (mono- and di-ethoxylate of nonylphenol and octylphenol), bisphenol A and steroids (estriol, estrone, 17beta-estradiol, 17alpha-estradiol, mestranol and 17alpha-ethynylestradiol) in aqueous and solid samples were developed. The proposed methods were applied for the determination of the target compounds in representative environmental samples in the area of Thessaloniki, Northern Greece. RECOMMENDATIONS AND PERSPECTIVES: This study confirms the occurrence of selected EDCs in inland and marine waters in the area of Thessaloniki, Northern Greece. Since there is no previous data on the occurrence of the target EDCs in the major area, an extended survey is in progress to evaluate the occurrence and fate of these compounds.     

HYSTAR Sediment Model: Distributed Two‐Dimensional Simulation of Watershed Erosion and Sediment Transport Using Time‐Area Routing

An erosion and sediment transport component incorporated in the HYdrology Simulation using Time‐ARea method (HYSTAR) upland watershed model provides grid‐based prediction of erosion, transport and deposition of sediment in a dynamic, continuous, and fully distributed framework. The model represents the spatiotemporally varied flow in sediment transport simulation by coupling the time‐area routing method and sediment transport capacity approach within a grid‐based spatial data model. This avoids the common, and simplistic, approach of using the Universal Soil Loss Equation (USLE) to estimate erosion rates with a delivery ratio to relate gross soil erosion to sediment yield of a watershed, while enabling us to simulate two‐dimensional sediment transport processes without the complexity of numerical solution of the partial differential governing equations. In using the time‐area method for routing sediment, the model offers a novel alternative to watershed‐scale sediment transport simulation that provides detailed spatial representation. In predicting four‐year sediment hydrographs of a watershed in Virginia, the model provided good performance with R² of 0.82 and 0.78 and relative error of ?35% and 11% using the Yalin and Yang's sediment transport capacity equations, respectively. Prediction of spatiotemporal variation in sediment transport processes was evaluated using maps of sediment transport rates, concentrations, and erosion and deposition mass, which compare well with expected behavior of flow hydraulics and sediment transport processes.     

土壤原位覆盖对底泥的修复作用研究

在高度厌氧底泥和富营养化水体构成的模拟生态系统中，采用土壤和硅藻土进行原位覆盖，研究了覆盖技术对水．沉积物界面微环境的改善作用和不同覆盖材料对苦草生长的影响。这2种底质覆盖后，表层底泥氧化还原电位（Eh）分别提高了48．37％和46．77％，底层水体的溶解氧消耗降低，水体中的总氮（TN）和总磷（TP）含量降低；与对照箱体的苦草死亡相比，经过土壤和硅藻土覆盖的箱体中苦草正常萌发、定植和生长；硅藻土箱体苦草的生物量、叶绿素和根茎比均高于土壤覆盖箱体。因此，原位覆盖能有效改善底层水体和表层底泥的氧化还原环境，隔绝污染底泥和延缓营养盐释放，为沉水植物种子萌发和幼苗生长提供有利的生境条件。     

Ecotoxicological evaluation of industrial port of Venice (Italy) sediment samples after a decontamination treatment

This work assesses the ecotoxicological effects of polluted sediment after a decontamination treatment process using a new sediment washing technique. Sediment samples were collected from four sites in Marghera Port industrial channels (Venice, Italy). Ecotoxicological evaluations were performed with Vibrio fischeri and Crassostrea gigas bioassays. Whole sediment and elutriate were deemed as the most suitable environmental matrices for this study. Toxicity scores developed in the Lagoon of Venice for V. fischeri on whole sediment and for C. gigas on elutriate were considered for the final ranking of samples. Ecotoxicological results showed that the treated sediment samples presented both acute and sub-chronic toxicities, which were mainly attributed to the presence of some remaining chemicals such as metals and polyaromatic hydrocarbons. The acute toxicity ranged from low to medium, while the sub-chronic one from absent to very high, suggesting that treated sediments could not be reused in direct contact with seawater.     

Temporal trends of hydrocarbons in sediment cores from the Pearl River Estuary and the northern South China Sea

Concentrations and fluxes of unresolved complex mixture of hydrocarbons (UCM) and polycyclic aromatic hydrocarbons (PAHs) were analyzed for two ²¹⁰Pb dated sediment cores from the Pearl River Estuary (PRE) and the adjacent northern South China Sea (NSCS). Compound-specific stable carbon isotopic compositions of individual n-alkanes were also measured for identification of the hydrocarbon sources. The historical records of PAHs in the NSCS reflected the economic development in the Pearl River Delta during the 20th century. PAHs in the NSCS predominantly derive from combustion of coal and biomass, whereas PAHs in the PRE are a mixture of petrogenic and pyrogenic in origins. The isotopic profiles reveal that the petrogenic hydrocarbons in the PRE originate predominantly from local spillage/leakage of lube oil and crude oils. The accumulation rates of pyrogenic PAHs have significantly increased, whereas UCM accumulation has slightly declined in the NSCS in the recent three decades.     

长江河口上边界床沙粒径的长期变化及其原因

大通水文站和泥沙观测断面位于长江河口的上边界。长江下游从大通（潮区界）至长江口门的距离长达680 km。20世纪80年代以来，长江流域日趋强烈的人类活动，显著改变了长江入海水文和泥沙数量和特性，从而对长江下游至河口动力地貌和动力沉积产生了显著影响。主要研究长江潮区界大通断面20世纪50年代以来床沙粒径的长期变化。1977~2004年床沙粒径 (〖WTBX〗d〖WTBZ〗50) 有一稳定增大的趋势，这主要是对上游河道悬沙来量持续减少的响应。值得注意的是床沙粗化过程是发生在该河床长期加积的背景上的。研究表明：导致床沙粒径粗化的原因，主要是上游河段进入本河段床沙粒径的增加和本河段冲淤过程中悬沙与床沙颗粒的交换。随着三峡水库的正常运行和其它大型水库的建设，预计未来几十年长江上游悬沙来量将进一步大幅度下降，可以预计，长江潮区界河段的床沙粒径将继续呈现增大的趋势。〖