The enrichment factor, multivariate analysis and metal speciation studies were used to identify degree, source and dispersal of metal contamination in Khli Ti watershed, Thailand. Topsoil samples were collected throughout the watershed, analyzed for total metal concentration. Sequential extraction was also carried out to determine geochemical phases of metals which were identified as exchangeable and bound to carbonates, Fe–Mn oxides, organic matter and residuals. Soil characteristics including pH, total organic carbon, redox potential, cation exchange capacity and texture were also analyzed. Principal component analysis yielded three metal groups which explained 83% of the variance. The concentrations of metals which were derived from lithogenic origin, such as Co, Cr, Fe, Ni and V were in natural background levels and were mostly bound to the residual phase. The remaining elements (i.e. Ba, Cd, Cu, Pb, Sb and Zn) were associated with the contamination from previous activities of the Pb-ore concentrator and Zn–Pb mining. Anthropogenic contamination mainly increased Pb and Zn bound to Fe–Mn oxides at the expense of residual fraction. Even though low exchangeable Pb contents in Khli Ti soils indicated low availability to plants, Pb bound to Fe–Mn oxides fraction might increase its mobility under reducing conditions.

Concentrations of mercury (Hg) were measured in six dated cores from four lakes in western Whatcom County, Washington, USA, that were at various bearings from a chlor-alkali plant, two municipal waste incinerators and a municipal sewage sludge incinerator. The importance of atmospheric emissions of Hg from these local municipal and industrial sources was evaluating by comparing the temporal trends in sedimentation of the lake cores with the emission history of each Hg species and by examining the geographical distribution of Hg sedimentation in relation to the region's primary wind pattern. Local municipal and industrial sources of atmospheric Hg were not responsible for the majority of the Hg in the upper layer of sediments of Whatcom County lakes because of (1) the significant enrichment of Hg in lake sediments prior to emissions of local industrial and municipal sources in 1964, (2) smaller increases in Hg concentrations occurred after 1964, (3) the similarity of maximum enrichments found in Whatcom County lakes to those in rural lakes around the world, (4) the inconsistency of the temporal trends in Hg sedimentation with the local emission history, and (5) the inconsistency of the geographic trends in Hg sedimentation with estimated deposition. Maximum enrichment ratios of Hg in lake sediments between 2 and 3 that are similar to rural areas in Alaska, Minnesota, and New England suggest that global sources of Hg were primarily responsible for increases of Hg in Whatcom County lakes beginning about 1900.

An assessment of the environmental quality of sediments at several locations of the Ría de Pontevedra (NW of Spain) was performed by integrating toxicity data obtained from multiespecies bioassays, chemical data from analysis of mussels and sediment, and physical-chemical parameters of the sampled sites. Subsequently, a toxicity identification evaluation (TIE) method intended for characterization and identification of the toxic agents was applied to the most polluted location by using the Paracentrotus lividus sea urchin bioassay. Both metals and organic compounds seem to be the causative agents of toxicity in elutriates of the studied sediment. Finally, multivariate statistics were applied for a better interpretation of results. A factor analysis was developed to establish the relationship among variables and to derive local sediment quality guidelines (SQG) by linking chemical contamination to biological effects. When multidimensional scaling and cluster analysis were performed to group the locations according to either the chemistry or toxicity data, P3-site was always clearly broken up the others. The different approaches all supported the same conclusion: site P3 can be considered highly contaminated by both trace metals and PAHs resulting in high toxicity for all the tested species.

The pulp left after the extraction of juice from Citrus reticulate (kinnow), is a waste material, which was used as a potential sorbent for Cr(III) and Cr(VI) in the present study. The effect of experimental parameters such as pH, biosorbent dosage, biosorbent particle size, initial metal concentrations, temperature, shaking speed and sorption time on the Cr removal is apparent from the obtained results. The Freundlich isotherm and pseudo second order kinetic models fitted well to the data of Cr(III) and Cr(VI) biosorption by Citrus reticulata waste biomass. Effect of several pretreatments such as gases, natural coagulant and many other chemicals on Cr(III) and Cr(VI) sorption capacity of Citrus reticulata waste biomass was first time analyzed in the present study. The metal sorption capacity of Citrus reticulata waste biomass after a specific pretreatment was not only related to the nature of chemical but also strongly dependent on the oxidation state of the metal.

Aluminium is a non-essential element for biological systems and is used in water and wastewater processes that rely on (micro)biological purification processes. The effect of Al doses ranging from 100 to 2,000 μg/l on the microbial dissolved oxygen uptake (respiration) over a 24-h period was assessed. Results indicated that Al can reduce the 24-h respiration, but the effects of pH depression due to Al dosing during testing should be taken into account.

The increase of traffic and the rising energy consumption mean a challenge to the air pollution control and to environmental protection. Measures of air pollution control concentrated primarily on the reduction of gaseous pollutants. However, in the field of air hygiene in Central Europe, especially the load of near-surface atmospheric dust becomes threatening to human health. A SIMS microprobe for ultra fine feature analysis is used to image the elemental composition at the surface of submicrometer urban dust particles collected at two measurement stations in the Grand Duchy of Luxembourg. The NanoSIMS 50 has been chosen because it creates one intensity image for each selected element in a high spatial resolution down to 50 nm. The atmospheric fine dust consists of a mixture of organic and inorganic compounds. The elemental composition at the surface of particles was studied using a global image segmentation technique to separate the signal from the background of the particles. The analysis of the binary intensity images was carried out using several shape and proximity measures. The patch shape complexity and distribution for industrial/urban particles were found to differ significantly from the solids collected from a forest site. We conclude that the methodology developed in the study is a reliable tool to differentiate between potential sources of airborne particulate matter.

This study presents the analysis of two series of concentrations of airborne particulate matter (APM) collected in two exploratory campaigns aimed at elucidating the source-receptor problem (SRP) in the metropolitan area of Buenos Aires. Although several techniques have been previously applied to interpret these measurements, we have almost exclusively used here the method of angular distances among objects (ADO) to discuss its advantages as a tool in understanding environmental questions within the source-receptor framework. We present a simple method of calculating the ADO, explain its chemical interpretation and the information that is possible to get by classifying the angular distances. A comparison among ADO with principal component analysis and Kohonen artificial neural networks is also discussed.

The major objective of this paper is to provide insights to sources and sinks of nitrous acid in urban areas, and their seasonal dependency on meteorology, photochemistry and long range transport. With this aim, nitrous acid (HONO) mixing ratios and other compounds were measured in Ashdod (south of Tel Aviv, Israel), a typical Mediterranean urban area. Statistical data analysis revealed the expected correlation between HONO and nitrogen oxides during the autumn campaign when HONO sources appeared to be traffic-, harbor-, and industry-related. Conversely, during summer HONO and NO₂ were no longer correlated: NO₂ at nighttime was probably deposited onto surfaces, soil and plants, whereas HONO at daytime was likely destroyed photolytically contributing to the OH concentration. Photolysis was expected to be the dominant HONO sink at daytime, especially during the summer period. Using modeled photolytical HONO lifetimes we estimate the magnitude of heterogeneous and/or organic electron transfer source reactions of HONO as 6-8 ppbv/h.

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.