Different nitrogen (N) fractions from 14 sediments from the shallow lakes in the middle and lower reaches of Yangtze River area before and after N release experiments were investigated, and the content of different N fractions, and contribution of different N fractions to the N released from sediments were also studied. Ion-exchangeable form (IEF-N), carbonate form (CF-N), iron-manganese oxide form (IMOF-N) and organic matter-sulfide form (OSF-N) accounted for 2.72~17.67%, 0.47~4.43%, 1.18~3.49% and 31.05 to 71.61% to total N, respectively. The N released was higher than 50% from IEF-N, approximately 35% from OSF-N, 6 and 8% from CF-N and IMOF-N on the average. Approximately 27.32~70.02% of IEF-N, 10.37~32.11% of CF-N, 11.37~33.43% IMOF-N and 2.02~8.19% OSF-N were released. For the sediments that were slightly polluted, IEF-N was the main N fraction that may be released and its contribution to total N released was more than 63.07%, for the sediments that TN was higher than 3,540.27 mg·kg-¹, OSF-N would become the main N fraction that can be released and its contribution to total N released was more than 45%.

The interaction between fluvially transported, metal contaminated peat particulates and acidic waters draining peatland catchments has received limited attention. Potential in-stream processing of sediment-associated metals in acidic stream water was investigated in laboratory based mixing experiments, designed to represent conditions of fluvial sediment transport in a highly contaminated and severely eroding peatland catchment in the Peak District (UK). Over the initial 20 min of the first experiment, stream water Cr and Zn concentrations increased by at least an order-of-magnitude and remained elevated for the full duration (24 h) of the experiment. Stream water As, Mo, Pb, Ti and V concentrations increased between 43% (As) and 440% (V) over the first hour of the experiment. After 24 h most of the metals appeared to have reached equilibrium in the water column. Results of the second experiment revealed that when the concentration of metal contaminated peat particulates is increased, there is an associated increase in the stream water As, Cr, Mo, Pb, Ti, V and Zn concentrations. The experimental data suggest that As, Cr, Mo, Pb, Ti, V and Zn are liable to desorption from metal contaminated peat into acidic stream water. The solubilisation of contaminated peat particulates may also contribute to elevated stream water metal concentrations. The laboratory based approach used in this study may indicate that when there is erosion of metal contaminated peat into acidic fluvial systems there is a concomitant increase in dissolved metal levels, especially when suspended sediment concentrations are high. Further laboratory and field based experiments are required to evaluate the relative importance of physical and chemical processes in the interaction between contaminated peat particulates and stream water in peatland fluvial systems.

Source apportionment analysis was used to identify the factors contributing to atmospheric pollution at a monitoring location in the Southeast of Spain, a well documented area with an arid climate and high insolation favouring two sources of particulate matter: secondary transformation in the atmosphere and resuspension of crustal dry soils to the air. These conditions are further complicated by numerous industrial facilities in the area of the historical city of Cartagena. This paper describes the air quality of an area which includes a zinc metallurgical industry, a petrochemical factory, an oil power station, a shipyard and natural phenomena including African dust transport and resuspension of regional and/or local crustal materials. Major and trace element concentrations in PM10 and PM2.5 were determined at two monitoring stations in Cartagena (one PM10 sampler located at a traffic hotspot and the PM2.5 sampler at a suburban station), during 2004 and 2005. Results showed that in the PM10 fraction, the zinc metallurgical activity was linked to high levels of Cd, Zn and Pb; shipyard emission was associated with high levels of Cr and Ni; and high Ni and V levels were associated with the secondary aerosol indicating the contribution from oil combustion (oil-fired power station or petrochemical facilities). In the PM2.5 size fraction, the zinc source is defined by Zn and Pb; V, Ni and As appear with the oil combustion emissions. In contrast to PM10, shipyard activity is not consistently defined. Consistent sources found in both size fractions include crustal materials and traffic emissions.

Phytoremediation, which mainly employs hyperaccumulators to remove heavy metals from contaminated soils, is receiving more attention world-wide. The identification of hyperaccumulators is still a key step for phytoremediation. This research is devoted to identify some plants with hyperaccumulative characteristics from weed species. In a pot culture experiment, the hyperaccumulative characteristics of 13 weed species in 11 families to Cd, Pb, Cu and Zn were examined. The result showed that Taraxacum mongolicum and Rorippa globosa indicated some Cd hyperaccumulative properties. In a sample-analysis experiment conducted in a Pb-Zn mining area, T. mongolicum and R. globosa also displayed the same hyperaccumulative characteristics. However, in a concentration gradient experiment, Cd content in shoot of T. mongolicum was not higher than 100 mg/kg (DW, dry weight), the minimum Cd concentration for a Cd-hyperaccumulator in any treatment. The concentration of Cd in the stems and leaves of R. globosa were greater than 100 mg/kg, under the conditions of the soils spiked with 25 and 50 mg/kg Cd. The Cd accumulation factors and translocation factors in the shoots of R. globosa were higher than 1 too, and the plant biomasses did not decrease significantly (p < 0.05) compared with the control. Thus, we conclude that only R. globosa showed the whole Cd-hyperaccumulator properties, which is a Cd-hyperaccumulator.

An elevated concentration of uranium in the water of some springs in the Permo-Triassic sedimentary rocks of the Visok region, south-eastern slopes of the Stara Planina, eastern Serbia, is interpreted based on geological, hydrogeological and hydrochemical data. Uranium concentration in groundwater was first examined whilst exploring for uranium minerals as an energy resource. The purpose of a later hydrogeological investigation was assessment of a safe drinking water supply to a planned ski-centre hotel. The maximum contaminant level for uranium, recommended by the World Health Organization (WHO), is 15 μg/L. This work reviews and interprets the naturally elevated uranium in springs from the Permo-Triassic sediments of Visok, focusing on geological, hydrogeological, hydrogeochemical and other factors of uranium contamination. Uranium distribution in groundwater from Permo-Triassic aquifers was studied by taking groundwater, spring sediment and rock samples. The varied mobility of uranium depends largely on lithology, which also controls the chemistry of groundwater. The investigation results have shown that sulfate-calcium groundwater is a suitable facilitator of uranium mobility with a high migration coefficient of 0.77. Uranium concentrations in this water were up to 41 μg/L, with a Sa/Sr mass ratio of around 20, and a mineral content of about 0.5 g/L. The hydrochemistry was characteristically transitional Eh and pH neutral. Elevated uranium in groundwater has been reported globally and may be compared.

Intensive cultivation of fen peat soils (Eutric Histosols) for agricultural purposes, started in Europe about 250 years ago, resulting in decreased soil fertility, increased oxidation of peat and corresponding CO₂-emissions to the atmosphere, nutrient transfer to aquatic ecosystems and losses in the total area of the former native wetlands. To prevent these negative environmental effects set-aside programs and rewetting measures were promoted in recent years. Literature results and practical experiences showed that large scale rewetting of intensively used agricultural Histosols may result in the mobilisation of phosphorus (P), its transport to adjacent surface waters and an accelerated eutrophication risk. The paper summarises results from an international European Community sponsored research project and demonstrates how results obtained at different scales and from different scientific disciplines were compiled to derive a strategy to carry out rewetting measures. A decision support system (DSS) for a hydrologically sensitive area in the Droemling catchment in north-eastern Germany was developed and is presented as a tool to regulate rewetting in order to control P release. It is demonstrated that additional laboratory experiments to identify essential processes of P release during rewetting and the site-specific management of the water table, the involvement of specific knowledge and experience of the stakeholders are necessary to develop an applicable DSS. The presented DSS is practically used to prevent freshwater resources from diffuse P pollution.

Meteorological factors affecting concentration of dissolved inorganic nitrogen in rain were examined. Rain samples were collected on an event basis from a location 100 km east of the Los Angeles Basin. Analysis of the data demonstrated a double decay function where small increases in rain volume resulted in large decreases in nitrogen concentration. In separate time series collections of individual storms, storm wind direction also influenced nitrogen concentrations

Concentrations of Cr, Cu, Hg, Pb and Zn have been measured, by atomic absorption spectrophotometry, in the fine fraction (<63 μm) of surface sediments collected in 30 sites in the Palermo Gulf (Sicily, Italy) in order to assess the levels and the spatial distribution of these elements. Enrichment factors calculated with respect to clean areas have been considered to discriminate between levels due to background or to pollution contributions. The sampling stations, which form a grid inside these areas, are characterized by geographic proximity and by the presence of pollution sources. Ratio matching technique along with hierarchical clustering, minimum spanning tree and principal component analysis have been used for the statistical analysis of data, allowing to better describe the spatial distribution of metal levels. Our work allowed to assess the anthropogenic contribution to the pollution of the area under investigation through industrial and domestic wastes, presence of an harbour area and river inflow.

Human exposure to volatile organic compounds (VOCs) and residential indoor and outdoor VOC levels had hitherto not been investigated in Turkey. This study details investigations of indoor, outdoor, and personal exposure to VOCs conducted simultaneously in 15 homes, 10 offices and 3 schools in Kocaeli during the summer of 2006 and the winter of 2006–2007. All VOC concentrations were collected by passive sampling over a 24-h period and analyzed using thermal desorption (TD) and a gas chromatography/flame ionization detector (GC/FID). Fifteen target VOCs were investigated and included benzene, toluene, m/p-xylene, o-xylene, ethylbenzene, styrene, cyclohexane, 1,2,4-trimethylbenzene, n-heptane, n-hexane, n-decane, n-nonane, n-octane and n-undecane. Toluene levels were the highest in terms of indoor, outdoor, and personal exposure, followed by m/p-xylene, o-xylene, ethylbenzene, styrene, benzene and n-hexane. In general, personal exposure concentrations appeared to be slightly higher than indoor air concentrations. Both personal exposure and indoor concentrations were generally markedly higher than those observed outdoors. Indoor target compound concentrations were generally more strongly correlated with outdoor concentrations in the summer than in winter. Indoor/outdoor ratios of target compounds were generally greater than unity, and ranged from 0.42 to 3.03 and 0.93 to 6.12 in the summer and winter, respectively. Factor analysis, correlation analyses, indoor/outdoor ratios, microenvironment characteristics, responses to questionnaires and time activity information suggested that industry, and smoking represent the main emission sources of the VOCs investigated. Compared with the findings of earlier studies, the level of target analytes in indoor air were higher for several target VOCs, indicating a possible trend toward increased inhalation exposure to these chemicals in residential environments.

Bacteria, fungi and viruses are often encountered in aerosols and they can be pathogenic or cause allergies following inhalation. Wastewater treatment facilities have been found to generate bioaerosols, which are transported by the prevailing winds downstream to areas that can be up to several hundred meters away. Bioaerosol formation has a significant effect on air quality in the vicinity of the treatment plants. The amount and characteristics of the formed bioaerosols depend on the aeration system employed at the aeration tank of the wastewater treatment facility. In this work we determined Enterobacteria in air and wastewater samples at the main wastewater treatment facility of the city of Chania (Crete, Greece). Concentrations of airborne bacteria were measured near the aeration and sedimentation tanks. Samples of airborne bacteria were taken by using Merck's MAS-100 bioaerosol collector followed by incubation and enumeration of the colonies. The use of different growth media enabled the separation and enumeration of several classes of microorganisms. As part of this study, Enterobacteria in air samples were also determined by filtration sampling followed by analysis of the collected microorganisms using DAPI staining to determine total cell counts (both viable and non-viable cells). Fluorescence in situ hybridization (FISH) with specific 23S rRNA probes was also used in order to identify specific groups of microorganisms (well known pathogens) present in the bioaerosols. The analysis was also performed in wastewater taken from the aeration and secondary sedimentation tanks in an effort to correlate the airborne bacteria with those in the wastewater.