The application of magnetite-immobilized chitin in pentachlorophenol (PCP) removal was demonstrated in this study. The physicochemical parameters for immobilization of chitin by magnetite, and for PCP adsorption using magnetite-immobilized chitin were optimized. For chitin immobilization, the optimized conditions were: magnetite to chitin (m:c) ratio at 1:2, initial pH 6, 25°C, 200 rpm and 60 min in batch system. The immobilization efficiency (IE) was 99.4% and immobilization capacity (IC) was 2.0 mg chitin mg-¹ magnetite. High initial pH (pH > 11) and temperature (>30°C) lowered the IE and IC. For PCP (10 mg l-¹) adsorption, the optimized conditions were: 1,500 mg l-¹ immobilized chitin, initial pH 6, 25°C, 200 rpm and 60 min in batch system. The removal efficiency (RE) was 57.9% and removal capacity (RC) was 5.4 mg g-¹. The adsorption ability of immobilized chitin decreased with pH and temperature increased. However, increasing the amount of immobilized chitin (24,000 mg l-¹) can increase the RE up to 92%. Both chitin immobilization and PCP adsorption exhibited Langmuir and Freundlich adsorption isotherms. Results in this study indicated that magnetite-immobilized chitin was a cost-effective and environmental friendly adsorbent to remove environmental pollutants such as PCP.

Lygeum spartum, Zygophyllum fabago and Piptatherum miliaceum are typical plant species that grow in mine tailings in semiarid Mediterranean areas. The aim of this work was to investigate metal uptake of these species growing on neutral mine tailings under controlled conditions and their response to fertilizer additions. A neutral mine tailing (pH of soil solution of 7.1-7.2) with high total metal concentrations (9,100 and 5,200 mg kg-¹ Zn and Pb, respectively) from Southern Spain was used. Soluble Zn and Pb were low (0.5 and <0.1 mg l-¹, respectively) but the major cations and anions reached relatively high levels (e.g. 2,600 and 1,400 mg l-¹ Cl and Na). Fertilization caused a significant increase of the plant weight for the three species and decreased metal accumulation with the exception of Cd. Roots accumulated much higher metal concentrations for the three plants than shoots, except Cd in L. spartum. Shoot concentrations for the three plants were 3-14 mg kg-¹ Cd, 150-300 mg kg-¹ Zn, 4-11 mg kg-¹ Cu, and 1-10 mg kg-¹ As, and 6-110 mg kg-¹ Pb. The results indicate that neutral pH mine tailings present a suitable substrate for establishment of these native plants species and fertilizer favors this establishment. Metal accumulation in plants is relatively low despite high total soil concentrations.

Lowland heath is an internationally important habitat type that has greatly declined in abundance throughout Western Europe. In recent years this has led to a growing interest in the restoration of heathland on agricultural land. This generally requires the use of chemical treatments to return soil chemical conditions to those appropriate for the support of heathland ecosystems. However, the potential for negative impacts on the environment due to the potential of these treatments to increase the availability of trace metals via raised soil acidity requires investigation. A large-scale field study investigated the effect of two chemical treatments used in heathland restoration, elemental sulphur and ferrous sulphate, on soil acidity and whether it is possible to predict the effect of the treatments on availability of two potentially toxic cations (Al and Cd) in the soil along with their subsequent accumulation in the shoots of the grass Agrostis capillaris. Results showed that both treatments decreased soil pH, but that only elemental sulphur produced a pH similar to heathland soil. The availability of Al, measured by extraction with 1 M ammonium nitrate, could not be predicted by soil pH, depth in the soil and total Al concentration in the soil. By contrast, availability of Cd could be predicted from these three variables. Concentrations of both Al and Cd in the shoots of A. capillaris showed no significant relationship with the extractable concentration in the soil. Results are discussed in light of the possible environmental impacts of the chemical restoration techniques.

Former mining activities lasting 140 years in the Ducktown Mining District, Tennessee, USA, has contaminated the streams draining the district with acid-mine drainage (AMD). North Potato Creek and its major tributary, Burra Burra Creek, are two of the most heavily AMD-impacted streams in the district. The removal of dissolved metals from the water in these creeks is largely attributable to the sorption of Cu, Zn, Co, Al, and Mn on suspended hydroxide precipitates of Fe. The fraction of trace metals remaining in solution decreases with increasing pH in the sequence Pb < Cu < Zn < Co. The concentration of Fe in solution also decreases with increasing pH due to the formation of ferric hydroxide precipitates which accounted for up to 81.4% by weight of the total suspended sediment. The concentration of suspended sediment substantially decreases as the water of North Potato Creek flows through a large settling basin, where 1.3 (±0.3) x 10⁶ kg/year of trace-metal-laden suspended sediment would be annually deposited. In spite of this attempt to purify it, the water discharged into the river is acidic (pH 3.6) and still contains high concentrations of dissolved trace metals, which would resorb on to suspended sediment and be ultimately transported to a downstream reservoir, Ocoee No. 3 Lake.

Four umbric A horizons from acid forest soils were acidified in a batch type experiment and its effect in the Al pools of the solid phase analysed by means of selective dissolution methods. The results showed that Al release accounted for the consumption of 85-99% of the added protons, and causes a decrease of 2-33% of the 'reactive' Al pool of the soil solid phase. In these A horizons, inorganic non-crystalline Al and high stability Al-humus complexes are the main sources of the dissolved Al. The contribution of the complexes with intermediate stability only was relevant in the more acid horizon developed from phyllites (P18-A). The increase of equilibration time from 96 to 720 h did not caused significant differences in the decrease of the 'reactive' Al pool suggesting the acid neutralising reactions occurred in less than 96 h. In most cases the quantity of released Al is in agreement with the decrease of the different reactive Al pools of the solid phase.

Polycyclic aromatic hydrocarbons (PAHs) are considered to be atmospheric pollutants and well-known human carcinogens. This study analyzes the pollution scenarios of PAHs in the aerosol of Higashi Hiroshima, Japan. We examined the characteristics, the influences of meteorological conditions, the distribution and seasonal variation of PAHs in aerosol samples collected from June 2000 to May 2001. The concentration of PAHs in the aerosol of Higashi Hiroshima was ranging from 11.8 to 157.5 μg/g with a mean concentration of 63.4 μg/g. Results showed that there is positive correlation between aerosol PAH concentrations and ambient temperature but a relatively little correlation with solar radiation. Seasonal variation was observed with a higher concentration during winter and lower concentration during summer. Apart from that, principal component analysis and molecular diagnostic ratios were also used to characterize and identify possible PAHs emission sources. Results obtained strongly suggested that vehicular emissions appeared to be the major source of aerosol PAHs in this study although other sources do have some degree of influence.

Solids and phosphorus found within urban stormwater have the potential to cause environmental damage to ecological systems in receiving waters. The evaluation of these pollutants in urban stormwater is usually undertaken by physico-chemical monitoring programs which sample streamflow for laboratory assessment. In this study, data from two such monitoring programs have been examined for the catchment characteristics which influence solids and phosphorus discharge behaviour and the potential for the use of surrogate indicators to predict streamflow concentrations. The study involved partitioning of the components on the basis of the dissolved and particulate fractions. Investigation of the physical and chemical behaviour of solids and phosphorus by univariate and multivariate data analysis techniques led to the identification of interrelationships among the measured parameters. Thus, using turbidity and conductivity, relationships were developed for suspended and dissolved solids. Similarly, relationships were developed for dissolved and particulate phosphorus using suspended and dissolved solids. These relationships have the potential to enhance rapid generation of vital information from site-based measurements and to reduce the requirements for laboratory-based analysis of indicator concentrations in urban stormwater.

Groundwater contamination by leakage and spill of petroleum hydrocarbons from underground storage tanks has been a major environmental concern. Among various remediation alternatives, the vacuum-enhanced free product recovery (VFPR) is an important technology to extract light nonaqueous-phase liquids (LNAPLs) from subsurface. However, efficient design of a VFPR system was challenging to practitioners, since the process of hydrocarbon removal is costly and time consuming. To address such a problem, an integrated study system for optimizing the VFPR process was developed through coupling a numerical modeling system, a multivariate regression technique and nonlinear optimization model into a general framework. A two-dimensional multiphase flow simulation system was provided for modeling VFPR processes. An iterative stepwise-inference regression (ISIR) method was advanced for establishing a linkage between remediation actions and system responses. A nonlinear optimization model embedded with ISIR was then established for generating desired operating conditions. The results from a case study demonstrated that the established optimization model could effectively analyze tradeoffs between various environmental and economical considerations, and provide effective decision supports for site remediation practices. Compared with the conventional stepwise-cluster analysis method, the proposed ISIR method was more efficient and reliable in approximating relationships between remediation actions and system responses, and could significantly enhance the robustness of optimization solutions.

A 3-D biological model was developed and coupled to a hydrodynamic model, i.e., Princeton Ocean Model, to simulate the seasonal variation and budget of dissolved inorganic nitrogen, phosphate, and silicate in Jiaozhou Bay. The modeled nutrients distribution pattern is consistent with observation. Silicate, the most important limiting element for phytoplankton growth, is characterized by consumption in spring, increase in summer and autumn, and accumulation in winter, whereas dissolved inorganic nitrogen and phosphorous have increasing trend with low rates in spring, due to excessive river loads. Phytoplankton plays an important role in nutrient renewal by photosynthesis and respiration processes. During an annual cycle, 7.83 x 10³ t N, 0.28 x 10³ t P, and 3.93 x 10³ t Si are transported to the bay's outer sea, i.e., the Yellow Sea, suggesting that Jiaozhou Bay is a significant source of nutrients for the Yellow Sea. The spatial distribution of nutrients is characterized by vertically homogeneous profiles, with high concentration inside the bay and low concentration toward the bay channel. These features are mainly governed by strong turbulent mixing, fluvial influx, water exchange rate, and Yellow Sea water intrusion. Numerical experiments suggest that the government should pay enough attention to proper layout of sewage drainage.

During the period from July 2002 to June 2004, the chemical characteristics of the rainwater samples collected in downtown São Paulo were investigated. The analysis of 224 wet-only precipitation samples included pH and electrical conductivity, as well as major ions (Na⁺, [graphic removed] , K⁺, Ca²⁺, Mg²⁺, Cl-, [graphic removed] , [graphic removed] ) and carboxylic acids (acetic, formic and oxalic) using ion chromatography. The volume weighted mean, VWM, of the anions [graphic removed] , [graphic removed] and Cl- was, respectively, 20.3, 12.1 and 10.7 μmol l-¹. Rainwater in São Paulo was acidic, with 55% of the samples exhibiting a pH below 5.6. The VWM of the free H⁺ was 6.27 μmol l-¹), corresponding to a pH of 5.20. Ammonia (NH₃), determined as [graphic removed] (VWM = 32.8 μmol l-¹), was the main acidity neutralizing agent. Considering that the H⁺ ion is the only counter ion produced from the non-sea-salt fraction of the dissociated anions, the contribution of each anion to the free acidity potential has the following profile: [graphic removed] (31.1%), [graphic removed] (26.0%), CH₃COO- (22.0%), Cl- (13.7%), HCOO- (5.4%) and [graphic removed] (1.8%). The precipitation chemistry showed seasonal differences, with higher concentrations of ammonium and calcium during autumn and winter (dry period). The marine contribution was not significant, while the direct vehicular emission showed to be relevant in the ionic composition of precipitation.