Atrazine biodegradation by immobilized pure and mixed cultures was examined. A pure atrazine-degrading culture, Agrobacterium radiobacter J14a (J14a), and a mixed culture (MC), isolated from an atrazine-contaminated crop field, were immobilized using phosphorylated-polyvinyl alcohol (PPVA). An existing cell immobilization procedure was modified to enhance PPVA matrix stability. The results showed that the matrices remained mechanically and chemically stable after shaking with glass beads over 15 days under various salt solutions and pH values. The immobilization process had a slight effect on cell viability. With the aid of scanning electron microscopy, a suitable microstructure of PPVA matrices for cell entrapment was observed. There were two porous layers of spherical gel matrices, the outside having an encapsulation property and the inside containing numerous pores for bacteria to occupy. J14a and MC were immobilized at three cell-to-matrix ratios of 3.5, 6.7, and 20 mg dry cells/mL matrix. The atrazine biodegradation tests were conducted in an aerobic batch system, which was inoculated with cells at 2,000 mg/L. The tests were also conducted using free (non-immobilized) J14a and MC for comparative purpose. The cell-to-matrix ratio of 3.5 mg/mL provided the highest atrazine removal efficiency of 40-50% in 120 h for both J14a and MC. The free cell systems, for both cultures, presented much lower atrazine removal efficiencies compared to the immobilized cell systems at the same level of inoculation.

This paper summarizes substance flow analyses for four organic substances in the City of Stockholm, Sweden: diethylhexyl phthalate (DEHP), alkylphenolethoxylates (APEO), polybrominated diphenylethers (PBDE) and chlorinated paraffins (CP). The results indicate that the stocks of APEO, PBDE and CP all are approximately 200-250 tonnes, whereas the DEHP stock is two orders of magnitude larger. Emissions can be linked to imported consumer goods such as electronics (PBDE) and textiles (APEO), and to construction materials (DEHP, CP). For several of the substances considerable amounts remain in the technosphere for a long time, even after use of the substance in new products has been eliminated. For example, the use of DEHP as plasticizer for PVC plastics in cables and floorings has more or less been phased-out, but still these applications make up a stock of some 20,000 tonnes (85% of the total DEHP stock in Stockholm) and emit 28 tonnes of DEHP annually (93% of overall emissions). Likewise, the use of chlorinated paraffins in sealants has been radically reduced, but there are 170 tonnes of CP in sealants in Stockholm making up 75% of the stock, and causing half of the emissions to water and air. These emissions are likely to continue for decades, and the stocks therefore have to be considered when analysing and managing the impact of urban substance flows on the environment.

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.

A column of soil, excavated from a contaminated landscape was evaluated by means of X-ray fluorescence analysis. The measurements were intended to assess the vertical distribution of heavy metals and toxic elements in the depth profile. To judge fitness for purpose of the analytical method used the element specific power functions were derived yielding the minimum detectable variations of analyte concentrations refer to the investigated soil profile. The required measurement uncertainty components caused by both the sampling procedure and chemical analysis were empirically estimated using a nested sampling design (duplicate method). For this purpose the full length of the soil core was divided into horizontal layers. From each selected layer (sampling target) two composite samples were taken by simple random sampling to represent the typical composition of the sampling target. The pool of measurement results, obtained for the nested sampling design finally was subjected to variance analysis. The evaluation of the estimated variance components in terms of the percentage of total variance confirmed fitness for purpose for the method used.

Littoral zones are characterized by gradients in depth and vegetation biomass, influencing nutrient retention capacity. A field experiment was conducted in a Phragmites australis dominated littoral zone to investigate nutrient retention and its effect on surface water quality. Measurements were done in mesocosms where water levels could be manipulated. Nutrient status was investigated along a gradient perpendicular to the shore during two growing seasons, one with a stable water level and one with a gradually decreasing water level. Nutrient concentrations in sediment, soil pore water and surface water were significantly lower in the vegetated than in the unvegetated zone. The negative correlations of nutrients in sediment and water, with nutrient contents of the vegetation suggest a direct effect of the vegetation. Nutrient uptake and biomass of the vegetation was higher in continuously flooded soils than in seasonally emerging sediments higher along the littoral gradient, probably due to the increased salinity in drained zones. Denitrification rate was highest in the unvegetated zone and was positively related to water level. Flooded littoral zones did result in a higher nutrient retention than drained zones. On small scale, for an optimal nutrient retention a fluctuating regime is not necessarily better suited than a stable water level, but on a larger scale it can substantially increase the width of the vegetated zone. It is important to optimize conditions for helophyte growth since the positive effect of vegetation on nutrient retention, at least at local scale, has been demonstrated in this study.

Four sand pit lakes, at the Rio de Janeiro Sand Mining District, were monitored from November 2003 to November 2005, in order to characterize their hydrogeochemistry aiming to provide information to their possible use as fishponds at the end of mining activities. The results show diluted waters (low electrical conductivity) with low pH (<4) and relatively high sulfate and aluminum concentrations. The major water components (in particular Fe, Mn, SiO₂, Al and SO₄) are related to water acidity, since it controls solubility of aluminum silicate minerals and Mn and Fe oxides. Fe, Mn and Al availability in these waters are probably associated to organic colloids formation. On the other hand, the SiO₂ content, as well as the decrease of sand mining in rainy season, may partially control Al availability by the formation of hydroxi-aluminum silicates. These geochemical processes together with the interruption of sand mining in the rainy season and the dilution of sand pit lakes water by rainwater can support the use of these pit lakes as fishpond for aquaculture.

Two kinds of common turfgrass, fescue and ryegrass, were grown in soils amended with 20 x 80% sludge compost (SC) in this research. The effects of SC on two kinds of soil and response of fescue and ryegrass to the SC amendment were studied. The results showed that urease activity, extractable content of Cu and Zn and Electrical conductivity of both soils increased while pH decreased with the increase of SC amendment. However, the change of these parameters also depended strongly on soil characteristics. Sludge compost at the <=40 and <=60% levels can improve growth of fescue and ryegrass, respectively. The biomass of fescue grown in substrate with 40% SC increased 27% in a red soil and 44% in a yellow loamy soil compared to the control. The biomass of ryegrass grown in substrate with 60% SC increased 120% in the red soil and 86% in the yellow loamy soil. Sludge compost amendment at these levels did not significantly affect soluble salt contents of soil or Cu and Zn in plant tissue. Therefore, rational use of sludge compost can take advantage of its beneficial effect as a nutrient source for plant production while avoiding the potential deleterious effects on soil and plant.

Urban rainfall-runoff residuals contain metals such as Cr, Zn, Cu, As, Pb and Cd and are thus reasonable candidates for treatment using Portland cement-based solidification-stabilization (S/S). This research is a study of S/S of urban storm water runoff solid residuals in Portland cement with quicklime and sodium bentonite additives. The solidified residuals were analyzed after 28 days of hydration time using X-ray powder diffraction (XRD) and solid-state ²⁹Si nuclear magnetic resonance (NMR) spectroscopy. X-ray diffraction (XRD) results indicate that the main cement hydration products are ettringite, calcium hydroxide and hydrated calcium silicates. Zinc hydroxide and lead and zinc silicates are also present due to the reactions of the waste compounds with the cement and its hydration products. ²⁹Si NMR analysis shows that the coarse fraction of the waste apparently does not interfere with cement hydration, but the fine fraction retards silica polymerization.

Total Suspended particulate matter (TSP) in urban atmosphere of Islamabad was collected using a high volume sampling technique for a period of one year. The nitric acid-perchloric acid extraction method was used and the metal contents were estimated by atomic absorption spectrophotometer. The highest mean concentration was found for Ca at 4.531 μg/m³, followed by Na (3.905 μg/m³), Fe (2.464 μg/m³), Zn (2.311 μg/m³), K (2.086 μg/m³), Mg (0.962 μg/m³), Cu (0.306 μg/m³), Sb (0.157 μg/m³), Pb (0.144 μg/m³) and Sr (0.101 μg/m³). On an average basis, the decreasing metal concentration trend was: Ca > Na > Fe > Zn > K > Mg > Cu > Sb > Pb > Sr > Mn > Co > Ni > Cr > Li > Cd [almost equal to] Ag. The TSP levels varied from a minimum of 41.8 to a maximum of 977 μg/m³, with a mean value of 164 μg/m³, which was found to be higher than WHO primary and secondary standards. The correlation study revealed very strong correlations (r > 0.71) between Fe-Mn, Sb-Co, Na-K, Mn-Mg, Pb-Cd and Sb-Sr. Among the meteorological parameters, temperature, wind speed and pan evaporation were found to be positively correlated with TSP, Ca, Fe, K, Mg, Mn and Ag, whereas, they exhibited negative relationships with relative humidity. On the other hand, Pb, Sb, Zn, Co, Cd and Li revealed significant positive correlations with relative humidity and negative with temperature, wind speed and pan evaporation. The major sources of airborne trace metals identified with the help of principle component analysis and cluster analysis were industrial emissions, automobile exhaust, biomass burning, oil combustion, fugitive emissions, resuspended soil dust and earth crust. The TSP and selected metals were also studied for seasonal variations, which showed that Na, K, Zn, Cu, Pb, Sb, Sr, Co and Cd peaked during the winter and remained lowest during the summer, while Ca, Fe, Mg and Mn were recorded highest during the spring.

A field survey on the concentration of chemical species in particulate matter and gaseous compounds at two monitoring sites with different site classifications (urban and rural) was conducted over three years. Total (particulate matter + gaseous compounds) concentrations at the rural site were significantly lower than those at the urban site for all species (sulfur [graphic removed] and SO₂(g)), nitrate [graphic removed] and HNO₃(g)), ammonium [graphic removed] and ammonia (NH₃(g)), and chloride (Cl⁻ (p) and HCl (g))), which is thought to reflect classification of the site. The difference in the sulfur concentration at the urban and rural sites was characterized by the difference in SO₂ (g) concentration. Further, a clear seasonality was observed for the nitrate species. The HNO₃ (g) concentration was high in the summer compared with other seasons at both the urban and rural sites. The [graphic removed] concentration levels were approximately the same as those of NH₃ (g) at both sites. The molar ratios of the particulate matter concentration to the total concentration showed different characteristics; the nitrate, ammonium and ammonia, and chloride species showed a clear seasonal variation: low in summer and high in winter and the values were similar regardless of the site. On the other hand, the sulfur species showed constant values at both the urban and rural sites, however the concentrations were significantly different for the two sites. Ammonium accounted for the largest proportion of cations in the particulate matter, regardless of the site classification. In contrast, [graphic removed] accounted for the largest proportion of anions at the rural site, whereas [graphic removed] was comparable to [graphic removed] at the urban site. Ammonia accounted for the largest proportion of all chemical species at both sites. Seasonal analysis of the proportional distribution in particulate matter and gaseous compounds provides information on atmospheric conditions.