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.

Two series of laboratory-scale vertical flow systems (flooded and nonflooded columns) were designed to compare nitrogen removal performance, nitrous oxide emission, and ammonia volatilization under different water levels upon treating diluted digested livestock liquid. In these systems, influent was supplied at three hydraulic loading rates (HLRs of 1.25, 2.5, and 5 cm day⁻¹) during stage 1 and the rates were doubled during stage 2 when the water levels of nonflooded columns were elevated from zero to half the height of the soil column. After hydraulic loading rates doubled, the average removal rates of total nitrogen in flooded columns varied from 1.27 to 2.94 g⁻² day⁻¹ and those in nonflooded columns ranged from 1.23 to 3.88 g⁻² day⁻¹. The T-N removal at an HLR of 10 cm day⁻¹ in the nonflooded column with an elevated water table level had higher efficiency than that in the flooded column, suggesting T-N removal is enhanced in the nonflooded column probably due to the improved coupled nitrification–denitrification process under the elevated water table level condition. On the other hand, there was a significant correlation (r ² = 0.532, p < 0.001) between the N₂O flux and redox potential that mainly corresponded to water levels and HLRs, suggesting anoxic or aerobic conditions stimulate N₂O emission by enhancing the nitrification (nitrification–denitrification) process. In contrast, NH₃ volatilization had a high flux in the anaerobic condition mainly because of flooding. Based on the experimental results, it is hypothesized a nonflooded condition with higher water table level (Eh range of −160 to +260 mV) would be suitable to reduce N₂O emission and NH₃ volatilization peak value by at least half while maintaining relatively efficient nitrogen removal performance.

A novel silicate mesoporous material, SBA-15 supported Fe₂O₃, was synthesized by post-synthesis method via ultrasonic-assisted route. The desulfurization test from a gas mixture containing 0.1 vol% H₂S was carried out over SBA-15 supported Fe₂O₃ in a fixed-bed system at atmospheric pressure and room temperature. The effects of the chemical nature of Fe₂O₃ and the textural properties of the material on desulfurization capacity were studied. Materials before and after the desulfurization test were characterized using nitrogen adsorption, XRD, TEM, FTIR, XPS, ICP and other standard methods. The characterization results suggest that modification process does not change the two-dimensional hexagonal mesostructure of SBA-15. Iron species disperses inside channels and the outside surface in the crystalline phase of iron oxide. The material with iron content of 31.3 wt% presented highest H₂S uptake capacity. Structural properties of the material also play important roles in desulfurization performance besides the catalytic effects of iron oxide. The basic feature of material and enough oxygen supply are benefit for the reaction. SBA-15 supported Fe₂O₃ can be an effective alternative to capture H₂S from gas streams.

The immobilization of lead by the reaction with phosphate bearing materials is a promising remediation method for contaminated soils. Low soluble neo-formed lead-phosphate phases similar to chloropyromorphite [Pb₅(PO₄)₃Cl], can control availability and mobility of lead in the environment, and consequently reduce human exposure, if soils are the main contamination pathway. We used three phosphate source materials [NaH₂(PO₄)₃, commercial superphosphate and phosphate rock] to study lead immobilization in soil and mining waste samples. Products were examined after 1, 3 and 6 months of contact. The samples are from a contaminated area by former Pb mining and smelting activities, in southeastern Brazil, where epidemiological studies showed high lead blood levels in local population. The PBET (physiological based extraction test) bioaccessibility test was used to measure changes in the amount of soluble lead after sample treatment. Results show that the most efficient phosphate source was NaH₂(PO₄)₃, which reduced lead solubility to 92% in acidic gastric conditions after the first month of contact. Superphosphate and phosphate rock also diminished Pb solubility, but the effect was more time dependent. None specific Pb-phosphate phases could be identified by XRD in whole treated samples, but the Pb-Ca-P elemental associations, observed on SEM images and EDS spectra of portions of the samples, combined with the reduced solubility, indicate that more insoluble lead phases were formed after the treatment. Based in these results, the in site phosphate application on soils to induce lead immobilization should be considered as a possible alternative to reduce human exposure at the area.

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.

This study reports the evaluation of chemical composition of a Black Vistula and White Vistula streams' waters taking into consideration both geological conditions of the stream's catchment area and different water' level related to seasonal variations in particular catchment ecosystem (high stage: beginning of the vegetation period; medium stage: vegetation period; low stage: final time of vegetation period). The complex data matrix (744 observations), obtained by the determination of major inorganic analytes (Cl⁻, NO₃ ⁻, SO₄ ²⁻, NH₄ ⁺, Na⁺, K⁺, Ca²⁺, Mg²⁺) in water samples by ion chromatography was treated by linear discriminant analysis and non-parametrical testing. In case of both streams obtained results indicate presence of two discriminant functions (DFs). The data variance explained by DFs is as follows: Black Vistula stream--first DF: 93.5%, second DF: 6.5%; White Vistula stream--first DF: 66.3%, second DF: 33.7%. In case of Black Vistula stream first DF allows distinction of medium, high and low waterstage related samples while second DF between high/low and medium water stage related samples. In case of White Vistula stream first DF allowed to distinguish between medium/high and low water stage related samples while second DF between medium and high water level samples. In case of both streams, the most informative DFs were related to geological conditions of investigated catchments (contents of Cl⁻, Na⁺, K⁺, Mg²⁺, Ca²⁺, SO₄ ²⁻), while the second to nutrient biocycle (mainly NH₄ ⁺ and NO₃ ⁻) related to slope's exposition and inclination.

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.

In a risk assessment study the environmental fate of the herbicide glyphosate was studied with the specific background of the presence of genetically modified (GM) plants. Aim was to simulate the environmental behaviour of glyphosate in sandy field soil lysimeters after multiple herbicide applications and under the presence of GM soybean and to test and enhance model reliability in the simulation of the herbicide fate including biodegradation in the soil and herbicide translocation in GM plants. The modelling of the herbicide behaviour in the present study was based on the pesticide transport model LEACHP and the model PLANTX to simulate the pesticide uptake by plants. Both models were implemented in the modular modelling system EXPERT-N. Glyphosate transport measurements and the mathematical modelling results indicate that due to the high sorption of glyphosate to the soil matrix and the high microbial capacities for glyphosate degradation in the lysimeter soil, leaching risk can be considered to be low. We confirmed that the introduction of more adequate conceptual descriptions of microbial response to pesticide and nutrient additions can contribute to a reduction in the uncertainty of pesticide degradation modelling. Moreover, the consideration of uncertainty in sorption, dispersivity and degradation parameters revealed a considerable variability in model output. The observed accumulation of glyphosate in roots and nodules was reproduced by the simulation results. Under the restriction that the prevailing model assumptions are valid, the simulation results indicate that glyphosate may accumulate also in beans of trangenic soybean.

Chemical ultraviolet (UV)-filters are used in sunscreens to protect the skin from harmful UV radiation which may otherwise cause sunburns and skin cancer. Commonly used chemical UV-filters are known to cause endocrine disrupting effects in both aquatic and terrestrial animals as well as in human skin cells. Here, source mapping and substance flow analysis were applied to find the sources of six UV-filters (oxybenzone, avobenzone, 4-methylbenzylidene camphor, octyl methoxycinnamate, octyl dimethyl PABA and homosalate) and to identify the most dominant flows of these substances in Denmark. Urban water, composed of wastewater and surface waters, was found to be the primary recipient of UV-filters, whereby wastewater received an estimated 8.5-65 tonnes and surface waters received 7.1-51 tonnes in 2005. In wastewater treatment plants, their sorption onto sludge is perceived to be an important process and presence in effluents can be expected due to a lack of biodegradability. In addition, the use of UV-filters is expected to continue to increase significantly. Not all filters (e.g., octyl dimethyl PABA and homosalate) are used in Denmark. For example, 4-MBC is mainly associated with self-tanning liquids and private import of sunscreens.

Nitrated Polycyclic Aromatic Hydrocarbons (NPAH) were determined in the suspended particulates collected in São Paulo (Brazil) and three other cities lying in the São Paulo State, (namely, Araraquara, Piracicaba and Paulínia), during August 2002 and July 2003. São Paulo samples represented a big difference between two groups of days, one of which characterized by heavy injection of pollutants released by industrial and agricultural activities. Most NPAH congeners identified in the atmosphere were among those usually associated to diesel exhaust, with the three important exceptions of 2-nitrofluoranthene, 2- and 4-nitropyrene. Daytime reactions seemed to promote decomposition of primary fluoranthene and pyrene. Trends of NPAH at all sites seemed to be associated to regional transport of polluted air through air masses passing over sugar cane plantations of São Paulo State.