Metal associations in anoxic sediments and changes following upland disposal†

The ecological effects of heavy metals in contaminated sediments are more determined by the chemical form and reactivity than by the level of accumulation. Dredging of anoxic sediments and disposal on land is attended by changes of redox conditions. Under oxidizing conditions some controlling solid compounds may change gradually thus changing the solubility of certain metals.

Chemical extraction experiments for estimating characteristic association forms of heavy metals in anoxic sediments were carried out, both under presence and absence of air during the analytical procedure. Drying of the sediment decreases the proportion of the sulfidic metal fractions to a stronger degree, and oxidized Cd and Zn are found in the most available, exchangeable fraction.

With respect to long‐term effects acidification of poorly buffered sludges after disposal on land is probably the most important factor affecting metal associations and mobility. For many metal examples a linear relationship has been found between decreasing pH values and increasing dissolved metal concentrations. To quantify these relationships and for better comparison of samples a simple test procedure is proposed which is based on pH differences before and after addition of acid.     

The cadmium adsorption capacity of contaminated marine sediments from Hong Kong

The binding capacity of Cd to the sediment particles determines the potential of Cd release from the sediments. An experiment was performed to evaluate the adsorption of Cd by contaminated sediments collected from three different locations in Hong Kong, i.e. Kwun Tong, North Point and Nam Tam Wan, having different degrees of pollution. Langmuir and Freundlich equations were used to evaluate the adsorption of Cd by the sediments. Adsorption isotherms obtained from the Freudlich and Langmuir equations were generally linear and the adsorption of Cd by the sediments was significantly correlated with the adsorption maximum and binding energy constant of the Langmuir equation, and equilibrium partition constant of the Freundlich equation. All sediments had a high Cd adsorption capacity and the highly organic contaminated sediments from Kwun Tong had the highest adsorption capacity of 24,272 mg kg^‐1 at pH8. The adsorption of Cd for all sediments increased with a rise in pH of the equilibrium solution and the total organic carbon content of the sediments. Therefore, a change in the sediment chemical equilibrium is likely to reduce the binding capacity.     

Spatial variability in characteristics and trace metal levels in sediments from watercourses

Assessing sediment quality requires sampling designs which address variability. Often however, only one sample or composited sample is collected at a sample site. Existing studies on sediment variability or sampling strategies primarily concern lake or marine sediments. Two rivers and one canal were sampled to assess sediment variability. Further, it was determined if sediment contamination in running water could be predicted by using visual criteria and/or knowledge of the presence of depositional and erosion areas. Metal concentrations and sediment characteristics were measured in different visually distinct areas of the river. At all sample sites the coefficient of variance was relatively high for most sediment characteristics (1.4‐ > 100%) and metal levels (15.3–63.6%). In one river the majority of sediment characteristics variation was between two sediment types and detected by visually distinct differences. Significant differences in cadmium and zinc concentrations were also detected. Contrary to what was expected, cadmium, and zinc levels were highest in the coarse fraction. No differences were found in the second river. In the canal a greater concentration of fine grained sediments and metals were found in the deep areas. It was not possible to predict sediment areas with the highest levels of metal contamination using visual criteria or knowledge of the erosion and sedimentation pattern of the river.     

Denitrification in bottom sediment near oil production facilities off the Louisiana Gulf Coast

There is little information on denitrification in Gulf of Mexico bottom sediment. Potential denitrification rates in surface sediment were measured along transects legs extending 0–800 m from two offshore oil production platforms. The average potential denitrification ranged from approximately 50 mg N m^?2 d^?1 in surface sediment near the platforms to 15 mg N m^?2 d^?1 in sediment 800 m from the platforms. Measured denitrification rates were correlated to a higher organic matter content in sediment nearer the platforms. This research examined only a small component of nitrogen processing in Gulf of Mexico sediment. Additional research should examine the effect of nitrogen loading and temporal and spatial variability on denitrification rate.     

Estimation of methane emitted by natural wetlands of Orissa: Based on case studies on three representative wetlands

The rapid increase in the concentration of greenhouse gases in our atmosphere has led to significant changes in global climate. Methane is second to carbon dioxide in terms of its contribution to global warming. The wetlands serve as a major natural source of methane. Orissa State, located on the east coast of India, has a number of natural wetlands. Three representative wetlands: Chilka – the largest semi-saline lake of Asia, Anshupa – a land-locked fresh water lake and Gahirmatha – a tidal flood plain of Bhitara Kanika region that has sprawling mangrove vegetation (extension of the Sunderbans of the Gangetic delta) were chosen for intensive monitoring of water and sediment quality, along with methane flux over a period of three years during 1997–2000. The average seasonal methane fluxes were integrated to arrive at the annual flux from each wetland category. Finally, those results were extended to other natural wetlands of Orissa to arrive at the average annual methane flux of Orissa State. This is useful in calculating the total budget of greenhouse gases of India.     

Mercury concentrations in the surface sediments of the intertidal area along the west coast of Peninsular Malaysia

Total mercury (Hg) levels in the intertidal surface sediments along the west coast of Peninsular Malaysia were analysed by using heat vaporization method. Total Hg levels in these sediments ranged from 3.00 to 201?µg?kg^?1 dry weight with a mean concentration of 60.0?µg?kg^?1 dry weight. More than 90% of the samples studied have the total Hg concentrations less than 150?µg?kg^?1 dry weight. Compare with the regional data and sediment quality guidelines, the Hg contamination in the intertidal area along the west coast of Peninsular Malaysia was not serious, except for a few sites that might have received anthropogenic Hg in the samples collected between 1999 and 2000. It is suggested that a similar study of heavy metals in the sediments of the west coast of Peninsular Malaysia be conducted regularly.     

Characterization and sources of PAHs in an urban river system in Beijing,China

Water samples from 20 locations on rivers in the Tongzhou District of Beijing were collected four times from July 2005 to March 2006. In addition, sediment samples were collected in July 2005. All samples were analyzed for 16 US Environmental Protection Agency (EPA) priority pollutants polycyclic aromatic hydrocarbons (PAHs). The concentration, distribution, seasonal variation, and sources of the 16 PAH compounds identified in the water samples, suspended particles, and surface sediments were then evaluated. The concentrations of PAHs in the water and suspended particle and surface sediment samples ranged from 87.3 to 1,890 ng l⁻¹, 1,330 to 27,700 ng g⁻¹, and 156 to 8,650 ng g⁻¹, respectively. These results demonstrated that rivers in the Tongzhou District of Beijing had a high level of PAH pollution, especially in the suspended particles. The highest and lowest concentrations of PAHs in the water samples were observed in summer and spring. However, the seasonal variations in the concentration of PAHs in the suspended particles were more complicated. The dominant compounds in the water, suspended particle, and surface sediment samples were two-, three- and four-ring PAH compounds, respectively. Ratio analysis illustrated that fuel-burning was the primary source of PAHs in the study area. Gasoline, diesel, coal, and coke oven sources were identified and the contributions of the different fuel-burning sources were then calculated using factor analysis and multiple linear regression. These analyses revealed that coal combustion, gasoline combustion plus coke oven emission, and diesel combustion accounted for 38.8%, 38.5%, and 22.7% of the PAHs in suspended particles, respectively.     

Historical trends of trace metals in a sediment core from a contaminated tidal salt marsh in San Francisco Bay

Sedimentation of metals preserves historical records of contaminant input from local and regional sources, and measurement of metals in sediment cores can provide information for reconstruction of historical changes in regional water and sediment quality. Sediment core was collected from Stege Marsh located in central San Francisco Bay (California, USA) to investigate the historical input of trace metals. Aluminum-normalized enrichment factors indicate that inputs from anthropogenic sources were predominant over natural input for Ag, Cu, Pb, and Zn. Among these, lead was the most anthropogenically impacted metal with enrichment factors ranging from 32 to 108. Depth profiles and coefficients of variation show that As, Cd, and Se were also influenced by anthropogenic input. The levels of these anthropogenically impacted metals decline gradually towards the surface due to regulation of the use of leaded gasoline, municipal and industrial wastewater discharge control, and closure of point sources on the upland of Stege Marsh. Although trace metal contamination is expected to be continuously declining, the rates of decline have slowed down. For lead, it is estimated to take 44, 82, and 153 years to decrease to probable effects level (112 μg/g), the San Francisco Bay ambient surface sediment level (43.2 μg/g), and the local baseline levels (5 μg/g), respectively. Some metals in surface sediments (0–6 cm) are still higher than sediment quality guidelines such as the probable effects level. To further facilitate the recovery of sediment quality, more efficient management plans need to be developed and implemented to control trace metals from non-point sources such as stormwater runoff.     

甲醇提取-吹扫捕集-气质联用法快速测定土壤中8种苯系物

采用甲醇提取-吹扫捕集的前处理方法并结合气相色谱-质谱仪来测定土壤样品中的8种苯系物。实验结果表明,8种苯系物在前处理过程中被有效提取出来并被准确定性和定量,对于低浓度样品也具有良好的实验效果。此方法的检出限为0.3～0.8μg/kg,测定下限为1.2～3.2μg/kg。加标低、中、高3种不同质量比的标准物质,经实验分析土壤中8种苯系物相对标准偏差(RSD)为2.1%～6.8%,加标回收率为91.0%～105%,与相关行业标准相比具有一定的优势。     

气体钻井突发性井壁失稳动力演化机理及试验研究

从致密砂岩损伤破坏的角度出发,综合考虑致密砂岩的物理力学性质、地应力、裂缝圈闭高压等因素,在分析孔隙压力、地应力、裂缝圈闭高压在突发性井壁失稳过程中所起的作用基础上,将气体钻井突发性井壁失稳具有强烈时间效应的动态力学过程分为孕育、突变、井筒运移和终止4个阶段。对裂缝圈闭高压、地应力作用下致密砂岩的加速损伤演化引起的突发性井壁失稳机理进行了阐述,裂缝圈闭高压是突发性井壁失稳的主要动力源,地应力对突发性井壁失稳起辅助作用。通过模拟实验表明,受地应力破坏后的致密砂岩岩体在有裂缝情况下,卸压初始时刻释放的能量是无裂缝时的5~10倍,且该能量与动力学失稳密切相关。