The use of three inorganic materials as potential immobilizers of metals in soils has been studied by monitoring metal availability by EDTA extraction, the Simple Bioaccessibility Extraction Test (SBET) and extraction with a mixture of organic acids (OA). The SBET test was the most suitable for risk assessment in soils of recreational areas. The materials were a 4A-type zeolite, tri-calcium phosphate and 'slovakite', a synthetic sorbent developed for remediation of metal-polluted soils. Adsorption/desorption experiments of metals by the isolated materials showed that all materials caused a strong retention of metals from solutions, with negligible release by dilution. When added to soils of three parks, zeolite and, to a much lesser extent, slovakite caused some increase in soil pH. Despite this increase of pH, zeolite is often the least effective amendment for decreasing metal availability estimated by any method, and even sometimes seems to cause some increase, as well as an increase of soil electrical conductivity. In contrast, slovakite causes a decrease of available metals as estimated by EDTA and SBET, but by SBET the effect seems to be steadily reduced after the first samplings, so that after 300 days the metals extracted by this method are very similar to the data for the blanks. Despite the differences in pseudo-total metal contents, few differences are noticeable among parks. In general, these amendments are scarcely efficient in the case of neutral urban soils like those studied here. Other techniques are needed for controlling and, eventually, decreasing metal pollution hazard in soils of recreational areas.

The effect of aeration rate on nutrient removal from slaughterhouse wastewater was examined in two 10-L laboratory-scale sequencing batch reactors (SBRs--SBR1 and SBR2) operated at ambient temperature. The contaminants in the slaughterhouse wastewater had average concentrations of 4,000 mg chemical oxygen demand (COD) L⁻¹, 350 mg total nitrogen (TN) L⁻¹ and 26 mg total phosphorus (TP) L⁻¹. The duration of a complete SBR operation cycle was 8 h and comprised four operational phases: fill (7 min), react (393 min), settle (30 min) and draw/idle (50 min). During the react phase, the reactors were intermittently aerated four times at 50-min intervals, 50 min each time. DO, pH and oxidation-reduction potential (ORP) in the reactors were real-time monitored. Four aeration rates--0.2 L air min⁻¹ in SBR1 for 70 days, 0.4 L air min⁻¹ in SBR1 for 50 days, 0.8 L air min⁻¹ in SBR2 for 120 days and 1.2 L air min⁻¹ in SBR1 for 110 days--were tested. When the aeration rate was 0.2 L air min⁻¹, the SBR was continuously anaerobic. When the aeration rate was 0.4 L air min⁻¹, COD and TP removals were 90% but TN removal was only 34%. When the aeration rates were 0.8 and 1.2 L air min⁻¹, average effluent concentrations were 115 mg COD L⁻¹, 19 mg TN L⁻¹ and 0.7 mg TP L⁻¹, giving COD, TN and TP removals of 97%, 95% and 97%, respectively. It was found that partial nitrification followed by denitrification occurred in the intermittently aerated SBR systems.

A recently designed two-chamber-lysimeter-test-system allows the detailed investigation of degradation, transport and transfer processes of ¹⁴C-labeled substances in soil-plant-atmosphere-systems under outdoor conditions. With this test system it is feasible to distinguish between ¹⁴C-emissions from soil surfaces and ¹⁴C-emissions from plant surfaces in soil monoliths under real environmental conditions. Special soil humidity sensors allow the measurement of soil water content near to the soil surface, in 1 and 5 cm depth. The behavior of organic chemicals can be followed for a whole vegetation period and a mass balance for the applied chemical can be established. Some selected results of the herbicides isoproturon and glyphosate - using the two-chamber-lysimeter-test-system - are presented to demonstrate its applicability for the identification and quantification of the processes that govern pesticide behavior in soil-plant-systems. Mineralization of ¹⁴C-isoproturon was very different in four different soils; the mineralization capacity of the soils ranged from 2 to 60%. Leaching of isoproturon in general was very low, but depending on the soil type and environmental conditions isoproturon and its metabolites could be leached via preferential flow, especially shortly after application. For the herbicide ¹⁴C-glyphosate no accumulation of residues in the soil and no leaching of the residues to deeper soil layers could be observed after three applications. Glyphosate was rapidly degraded to AMPA in the soil. Glyphosate and AMPA were accumulated in soy bean nodules.

Otoliths of black bream (Acanthopagrus butcheri) collected from the Swan River Estuary were analysed by Laser Ablation Inductively Coupled Plasma Mass Spectrometry (LA-ICP-MS) to measure concentrations of 14 trace metals. Trace metal concentrations in the otoliths may be related to the environmental exposure history of fish to contamination. The following metal isotopes were investigated: aluminium (²⁷Al), calcium (⁴⁴Ca), manganese (⁵⁵Mn), iron (⁵⁷Fe), copper (⁶⁵Cu), zinc (⁶⁶Zn), strontium (⁸⁸Sr), cadmium (¹¹¹Cd), tin (¹²⁰Sn), barium (¹³⁸Ba), mercury (²⁰²Hg), lead (²⁰⁸Pb) and the metalloids arsenic (⁷⁵As, ⁷⁷As) and selenium (⁸²Se). Significant differences in otolith trace metal composition were found between sampling sites. Lead and ⁵⁷Fe were consistently lower in downstream fish relative to upstream fish, while ⁸⁸Sr varied with the salinity gradient in the urban estuary. Lead and ⁵⁷Fe followed similar patterns within the otoliths, and appeared to provide the best discriminatory power for relating otolith metal concentration to the environmental history of the fish.

The dust fall in a region is closely related to upwind sources. Dust fall from sandstorms has a strong influence on industry, agriculture, and daily life. Hohhot, the capital of Inner Mongolia Autonomous Region, is downwind of the Inner Mongolia Plateau and experiences frequent sandstorms during the spring monsoon season. This study investigated the relationship between dust fall in the Hohhot area and surface soils on the Inner Mongolia Plateau. Samples of dust fall from Hohhot and surface soils from the plateau were analyzed for major and trace elements. The SiO₂ content of dust fall from sandstorms differs from that of the plateau soils by only 2.77%, indicating that the main dust fall source for Hohhot is surface soils from the plateau. Dust samples from coal smoke, roads, and buildings were used for comparison. The As content in dust fall from sandstorms is greater than that found in the plateau soils and in dust from non-sandstorm days. This indicates that As is added to the sand during transport from the plateau by coal factories near Hohhot. The second most important dust source is traffic, as evidenced by Pb contents. Preventing erosion of sand upwind of Hohhot during the spring monsoon is key to improving and managing air quality in the Hohhot region. This can be accomplished through management of the farm grassland areas.

An experiment of Randomized Block Design was conducted during 2005 in a greenhouse of the University of Ioannina, Department of Environmental Management and Natural Resources, in order to study the effect of the Treated Municipal Wastewater (TMWW) on the interrelationships of macro, micronutrients, heavy metals and physical and chemical properties of a soil cultivated with Brassica oleracea var. italica (broccoli). The experimental design included the following treatments: (a) TMWW, (b) Fresh irrigation water or “control”, in six replications, with a total number of 2 x 6 = 12 plots of 2.5 x 1.8 = 4.5 m² size. The following were found. Numerous interactions are taking place in the soil under the effect of TMWW, between: (a) macro-, micronutrients, and heavy metals, i.e. (N, P, K, Ca, Mg, Zn, Mn, Fe, B, Cu)x(Ni (Co, Pb, Cd) and (b) between all the above metals and the soil properties i.e. (nutrients and heavy metals)x(pH,CaCO₃, O.M) These interactions could have an important impact on plant growth and the environment, as they can either supply the plants with nutrients, due to their synergistic effects or they can contribute to the decrease or inactivation (fixation) of some undesirable soil heavy metals, owing to their antagonism. Examples of these interactions are studied, and their significance in plants and the environment, is examined, under the effect of the TMWW reuse.

A fungal strain possibly capable of removing hexavalent chromium was to be isolated from industrial effluent from a leather factory located in the city of Guadalajara, state of Jalisco, Mexico. The strain was identified as Trichoderma inhamatum by the D1/D2 domain sequence of the 28S rDNA gene. Batch cultures of T. inhamatum in media containing initial Cr(VI) concentrations from 0.83 to 2.43 mM Cr(VI) were prepared. Experimental results suggest that the fungus is capable of transforming hexavalent chromium to trivalent chromium; a transformation of a highly toxic contaminant to a low toxic form. The specific and volumetric rates of Cr(VI) reduction by T. inhamatum cultures decreased as the initial Cr(VI) concentration increased. The fungus exhibited a remarkable capacity to tolerate and completely reduce Cr(VI) concentrations up to 2.43 mM. These results indicate that the T. inhamatum fungal strain may have potential applications in bioremediation of Cr(VI)-contaminated wastewaters.

The purpose of this study was to determine the degree of PAH contamination and the association of PAHs with metals in urban soil samples from Sevilla (Spain). Fifteen polycyclic aromatic hydrocarbons-PAHs (naphthalene, acenaphthene, fluorene, phenanthrene, anthracene, fluoranthene, pyrene, benzo[a]anthracene, chrysene, benzo[b]fluoranthene, benzo[k]fluoranthene, benzo[a]pyrene, dibenzo[a,h]anthracene, benzo[g,h,i]perylene, indeno[1,2,3-c,d]pyrene) and seven metals (Cd, Cr, Cu, Mn, Ni, Pb, Zn) have been evaluated in representative urban soil samples. Forty-one top soils (0-10 cm) under different land use (garden, roadside, riverbank and agricultural allotment) were selected. PAHs from soil samples were extracted by sonication using dichloromethane. The simultaneous quantification of 15 different PAH compounds were carried out by HPLC using multiple wavelength shift in the fluorescence detector. For qualitative analysis a photo diode-array detector was used. Metal (pseudo-total) analysis was carried out by digestion of the soils with aqua regia in microwave oven. The mean concentration of each PAH in urban soils of Sevilla showed a wide range, they are not considered highly contaminated. The results of the sum of 15 PAHs in Sevilla soils are in the range 89.5-4004.2 μg kg-¹, but there seems not to be a correlation between the concentration of PAHs and the land use. Of the 15 PAHs examined, phenanthrene, fluoranthene and pyrene were present at the highest concentrations, being the sum of these PAHs about 40% of the total content. Although metal content were not especially high in most soils, there are significant hints of moderate pollution in some particular spots. Such spots are mainly related with some gardens within the historic quarters of the city. The associations among metals and PAHs content in the soil samples was checked by principal components analysis (PCA). The largest values both for 'urban' metals (Pb, Cu and Zn) and for PAHs were mainly found in sites close to the historic quarters of the city in which a heavy traffic of motor vehicles is suffered from years.

The competing ligand exchange method was used to investigate the competitive binding of Ni(II) by Al(III) and Fe(III) in model aqueous solutions and freshwaters. Graphite furnace atomic absorption spectrometry and adsorptive cathodic stripping voltammetry were used to monitor the rate of uptake of the Ni by Chelex 100 chelating resin and dimethylglyoxime as the competing ligands, respectively. The results have revealed that Ni(II)-humate complexes were more labile in presence of the mixture of Al(III) and Fe(III), compared to the lability of the Ni(II)-humate complexes when only one of the two, Al(III) or Fe(III), was present. The environmental significance of this work is that in model solutions simulating freshwater containing humic substances and the target trace metal Ni(II) and cations, Al(III) and Fe(III), the competitive binding of Ni(II), Al(III) and Fe(III) by humic substances makes Ni(II)-humate complexes labile, releasing free Ni²⁺-aqua complex, which reported to be toxic.

In this study, heavy metal content (Cr, Cu, Mn, Ni, Zn) was determined in sediments and different organs of Rumex obtusifolius L. and Polygonum lapathifolium L. (Polygonaceae), Urtica dioica L. (Urticaceae) and Xanthium strumarium L. (Asteraceae) species. These species grow ubiquitously and vigorously on the periodic flooding areas of Nilüfer stream which have been polluted by different local industrial activities. Below and above-ground parts of plant samples and their sediments were analyzed by ICP-MS for their elemental contents. In general, the variations in the heavy metal content in sediments are reflected in heavy metal status of plant organs. However, this variation depends on plant species and heavy metals. R. obtusifolius, U. dioica and X. strumarium species have elevated levels of Cr, Cu, Ni, and Zn whereas Mn was observed only in P. lapathifolium. The contribution of different organs to the accumulation capacity of the total phytomass is specific to species.