In order to estimate acute-to-chronic toxicity ratios (ACRs) relevant to a coldwater stream community, we exposed rainbow trout (Oncorhynchus mykiss) to cadmium (Cd), lead (Pb), and zinc (Zn) in 96-h acute and 60+ day early-life stage (ELS) exposures. We also tested the acute and sublethal responses of a mayfly (Baetis tricaudatus) and a midge (Chironomus dilutus, formerly C. tentans) with Pb. We examine the statistical interpretation of test endpoints and the acute-to-chronic ratio concept. Increasing the number of control replicates by 2 to 3x decreased the minimum detectable differences by almost half. Pb ACR estimates mostly increased with increasing acute resistance of the organisms (rainbow trout ACRs <[almost equal to] mayfly < Chironomus). The choice of test endpoint and statistical analysis influenced ACR estimates by up to a factor of four. When calculated using the geometric means of the no- and lowest-observed effect concentrations, ACRs with rainbow trout and Cd were 0.6 and 0.95; Zn about 1.0; and for Pb 3.3 and 11. The comparable Pb ACRs for the mayfly and Chironomus were 5.2 and 51 respectively. Our rainbow trout ACRs with Pb were about 5-20x lower than earlier reports with salmonids. We suggest discounting previous ACR results that used larger and older fish in their acute tests.

Understanding and controlling air pollution in highly populated areas is very important, although interpreting the levels of gaseous pollutants and airborne particulate matter is complicated by dominant natural and anthropogenic emissions, micro-meteorological processes, and chemical reactions which take place directly in the atmosphere. For this reason, it is very difficult to relate the characteristics of air pollution to one or more specific emission sources. The aim of this paper is to detect associations among elements and organic compounds emitted from specific sources by means of chemical analyses, statistical processing of data, seasonal evolution study, and geochemical considerations to trace their origin. A detailed characterization of air quality during the period September 2000-September 2001 was carried out in three locations of the Venice region: A heavy traffic urban site, a public park, and the island centre of the city of Venice. Twenty-eight inorganic elements, four polycyclic aromatic hydrocarbons, CO and benzene were quantified and processed by a statistical procedure based on factor analysis considering variations on a seasonal basis. Results show the presence of associations between elements and compounds with the same behaviour in all sampling points. This indicates that several pollutants originate from a common source, and are then “diluted” throughout the study area, maintaining the imprint of their origin. Pt, polycyclic aromatic hydrocarbons, CO and benzene originating from the exhaust gas of vehicles are all linked in the traffic factor, whereas Cd is associated with Se, having a common source in industrial processes.

Lake St. Pierre (LSP), constituted of a 120 km² stretching of the St. Lawrence River (Southern Québec), hosts the largest freshwater fishery industry in Canada. The lake drains, through its main tributaries, an important area of agrarian land and was subjected to intense industrial activities in the past century. In this paper, we present (1) an estimation of the seasonal aquatic mercury (Hg) inputs to LSP from the St-Lawrence River and two major tributaries; (2) a reconstruction, by the analysis of sediment cores, of the historic inputs of Hg into LSP and in a large riparian wetland, Bay St. François. Our results indicate that the aquatic Hg inputs to LSP (290 kg Hg between April 2003 and April 2004) are moderately elevated with most of the inputs occurring from the St. Lawrence River, either in spring or early winter, during high flow episodes. The sediment profiles suggest a recent decrease in Hg inputs, likely attributable to improvements of industrial practices. The observed perturbation of the surface sediments give evidence of an active hydrodynamic regime, suggesting that LSP could only act as a transitory system for suspended sediment and Hg, with seasonal accumulation and recurrent re-suspension resulting from changes in the hydrodynamic regime. Finally, we observed positive MeHg fluxes from the sediment to the water at different seasons in Bay St. François. However, Hg levels in fish like walleyes of LSP are reported to be low, which could be explained by faster fish growth rates following in part intense fishing pressure in LSP.

The direct spectrophotometric analysis of aqueous nitrates is a simple analytical procedure but prone to interferences. A twelve-month study of the Preakness Brook in Wayne Township, New Jersey demonstrated that two wavelength, three wavelength, and second derivative calculation methods provide very different results from the same ultraviolet absorption spectrum. On average, the two wavelength and second derivative methods yielded the same concentration at each sample point over the entire study period. These methods provided concentration results closest to those obtained by ion chromatography and significantly lower than the three wavelength computation method. The degree of variation between the different computation methods was not consistent as it rose with increasing absorbances at wavelengths associated with interfering compounds. This variation was especially pronounced between May and August.

In recent years, arsenic (As) has received increased attention as humans may be exposed to it through occupational and environmental exposure. Tobacco (Nicotiana tabacum L.) like other crops can uptake this element from the soil, which may lead to human exposure. Here, we report on a survey on arsenic in cured or processed tobacco leaves obtained from Africa, Asia, Europe, South and North America. A total of 1,431 leaf samples of flue-cured, burley, and Oriental tobaccos were obtained from various sampling locations during 2002 to 2004. Arsenic concentration in the samples averaged 0.4 ± 0.6 μg g⁻¹ as determined by inductively coupled plasma-mass spectrometry. Recorded values from most samples showed that concentrations of arsenic were usually found at the lower end of the distribution. Significant differences were found among tobacco types, sampling locations, and crop years. Arsenic concentrations were rather low in the majority of regions investigated, which is compatible with data from the literature. However, sample size was small and sampling geographically restricted. Our results would need to be validated with a larger dataset.

Fluoride, a common phytotoxic air, water and soil pollutant is commonly released to the environment by a number of industrial processes. Agricultural soils high in fluoride are common due to long term accumulation of fluoride from multi-sources and extensive application of phosphate fertilizers. The effect of sodium fluoride (0, 50,100,150 mM) on growth, pigments content, changes in biochemical parameters, along with fluoride and other ions accumulation was investigated in Salicornia brachiata grown in solution cultures under controlled conditions. With fluoride treatment growth as fresh or dry mass accumulation increased marginally. However, higher concentrations decreased the biomass and shoot tip became blunt; margin of the shoot changed its colour to reddish brown and developed necrotic spots. Photosynthetic pigments (chlorophylls and carotenoids) content decreased, while, anthocyanin content increased significantly with fluoride treatment. Peroxidase (POX), superoxide dismutase (SOD), ATPase and acid phosphate activities were negatively regulated. In addition F-, Na⁺, Mn²⁺ and Fe²⁺ ions concentration increased while, K⁺, Ca²⁺ and Mg²⁺ contents decreased with fluoride treatment. To our knowledge this is the first report on fluoride tolerance in a marshy halophytes using as high as 150 mM concentration and the results suggest that S. brachiata is a moderately fluoride tolerant annual halophyte and may be useful to vegetate the fluoride contaminated marshy lands.

Soil and water samples were analysed for trace metals and As in two watercourses and 14 sampling plots in a salt marsh polluted by mine wastes in SE Spain. Groundwater levels, soil pH and Eh were measured 'in situ' for a 12-month period in each sampling plot, and total calcium carbonate was also determined. Low concentrations of soluble metals (maximum Mn 1.089 mg L-¹ and maximum Zn 0.553 mg L-¹) were found in the watercourses. However, total metal contents were extremely high in the soils of a zone of the salt marsh (maximum 1,933 mg kg-¹ of Mn, 62,280 mg kg-¹ of Zn, 16,845 mg kg-¹ of Pb, 77 mg kg-¹ of Cd, 418 mg kg-¹ of Cu and 725 mg kg-¹ of As), and soluble metals in the pore water reached 38.7 mg L-¹ for Zn, 3.15 mg L-¹ for Pb, 48.0 mg L-¹ for Mn, 0.61 mg L-¹ for Cd and 0.29 mg L-¹ for As. Variable concentrations with depth indicate a possible re-mobilisation of the metals, which could be related to spatial and temporal variations of water table level, pH and Eh and to the presence of calcium carbonate. A tendency for the Eh to decrease in the warmest months and to increase in the coldest ones was found, especially, in plots that received water with a high content of dissolved organic carbon. Hence, the existence of nutrient effluent-enriched water may modify the physical-chemical conditions of the soil-water system and influence metal mobility.

POPs are still a priority environmental problem, but can be used as a scientific tool for understanding the distribution phenomena. Both high mountains and polar areas are seen as priority zones for contamination studies. In this context, two altitudinal series of soil samples were analysed for several classes of Persistent Organic Pollutants (PCBs, DDTs, HCHs, HCB and chlordane). Two transects were carried out - one in the Peruvian Andes (Cordillera Blanca) and the other in the Italian Alps (Mount Legnone). In these two areas, POP composition and levels both gave different results, linked to regional emission history. The Italian samples were characterized by high levels of industrial type compounds, and by surprisingly high DDT contamination, due to a defined consistent local source in Northern Italy. The Peruvian samples, on the other hand, were characterized by generally low POP levels with relatively high DDT contamination. The concentration increase in line with elevation was evident only in the Italian transect, where higher precipitation intensities and an increasingly higher precipitation gradient in accordance with altitude was found present. Precipitations are considered a key factor for enhancing the condensation effect at high altitudes and for reducing summer revolatilisation, as they lower soil temperature. In the Italian altitudinal gradient, evidence of fractionation processes, with a shift of the PCB composition towards less chlorinated congeners, and a vegetation effect with a mean woodland/grassland enrichment factor between 2 and 4 were also observed.

Dry and wet deposition of atmospheric nitrogen species (NO₂ and HNO₃) coming from nitrogen oxides emissions in Buenos Aires city to surface waters of de la Plata River were estimated. Atmospheric dispersion models DAUMOD-RD (v.2) and CALPUFF were applied to area and point sources, respectively. These models were run considering 1 year of hourly meteorological data. Emission information included a typical diurnal variation of area source emissions. Annual atmospheric nitrogen (N-NO₂ + N-HNO₃) deposition to 1,763 km² of the river was 35,600 kg-N year⁻¹. Dry deposition processes accounted for 89% of this value. The small contribution of wet deposition was a consequence of the very few cases (5%) of rain events during offshore wind conditions. Monthly dry deposition to 1,763 km² of the river varied from 1,628 kg-N month⁻¹ in February to 3,799 kg-N month⁻¹ in December, following the monthly occurrence of offshore winds. Monthly wet deposition varied from 1 kg-N month⁻¹ in June to 1,162 kg-N month⁻¹ in February. These results came from the combination of favorable conditions for formation of HNO₃ and the occurrence of precipitation during offshore wind situations. Spatial distribution of annual atmospheric N deposition showed a strong coastal gradient. Deposition values reached a maximum of 137.1 kg-N km⁻² year⁻¹ near the shoreline, which was reduced to the half at 4 km from the coast.

The chemical composition of precipitation in the city of Mersin on the Mediterranean coast of Turkey has been studied. Spatial and temporal variability of rainwater constituents have been determined from samples collected at two central and two suburban stations for the December 2003-May 2005 period. A total of 246 samples covering all precipitation events were analyzed to determine pH, conductivity, as well as major anion (Cl-, [graphic removed] , [graphic removed] ); major cation (H⁺, Na⁺, K⁺, Ca²⁺, Mg²⁺, [graphic removed] ) and formaldehyde (HCHO) concentrations. The pH varied within a range of 4.8-8.5, with only 8 out of 246 samples being acidic (pH < 5.6), and the remaining highly alkaline samples being neutralized by either [graphic removed] in rainwater, or by CaCO₃ resulting from wet deposition of atmospheric dust. The volume weighted mean ΣAnion/ΣCation ratio was 0.49. The equivalent concentration of major ionic species followed the order: [graphic removed] . Formaldehyde concentrations varied in the range of 0.01-17.9 μM, and was found to be dependent on precipitation volume. Relatively higher [graphic removed] , [graphic removed] , [graphic removed] and HCHO concentrations, mainly of anthropogenic origin, measured near the city center suggest increased pollution from local anthropogenic sources, e.g., residential heating, industrial and/or traffic emissions. In general, the results of this study suggest local precipitation chemistry is more strongly influenced by natural (mineral dust and marine) sources compared to anthropogenic ones.