Single-particle analysis of short-term aerosol samplings can provide unique information on the rapid evolution of size distribution and chemical composition of industrial aerosols. In this work, the potential of scanning electron microscopy equipped with energy-dispersive X-ray spectrometry (SEM-EDX) for the time-resolved description of physicochemical properties of individual aerosol particles is investigated. Two sampling campaigns were carried out at a densely populated and industrialised coastal site. The first sampling campaign corresponded to low and stable atmospheric particle loads. Low temporal variations in PM₁₀ and PM₂.₅ mass concentrations during the preceding hours and during samplings were observed. In these conditions suitable to evaluate the accuracy of our sampling and analytical methodologies, very low temporal variation of physicochemical characteristics of atmospheric particles were observed, as expected. During the second sampling campaign, the ability of automated SEM-EDX to describe short temporal variation in PM₁₀ and PM₂.₅ chemical composition was demonstrated. We report the tracking of a steelworks emission plume transported over an urban area by means of short-term aerosol samplings and explore how this transient industrial emission contributed to ambient particulates. Steelworks are important point-source emitters of metallic pollutants such as iron, manganese, and zinc species. Detailed assessment of the microphysical and chemical properties of aerosols collected in the vicinity of steelworks enables to precisely describe how industrial aerosols affect the composition of urban particulate matter. The studied pollution event caused dramatic changes in the composition of urban aerosols by an input of fine metallic particles containing Fe, Mn or Zn oxides and mixed particles (Mn-Fe, Zn-Mn, Zn-Fe oxides). Metal-rich particles were often found internally mixed with marine and/or continental compounds, demonstrating how industrial aerosols efficiently coagulate with particles from other sources, thereby acting as carriers of heavy metals.

Despite many efforts for pollution abatement in aquatic ecosystems, there are still some cases of high accumulation of industrial pollutants due to past activities. In Flix reservoir (Ebro River, Spain), there are around 200,000-360,000 tons of industrial pollutants with a high concentration of heavy metals and organochlorides due to the activity of an organochlorine industry during more than half a century. This exceptional amount of pollutants provides a good opportunity (and need) to analyse their effects on fish populations under natural conditions, which is rarely available to ecotoxicologists. We compared the reproductive traits and prevalence of diseases and parasites at this impacted area with a neighbouring upstream reservoir unaffected by the pollution (reference sites) and also to downstream sites. Deformity, eroded fin, lesion and tumour (DELT) anomalies and ectoparasites were clearly more frequent at the impacted area for several fish species (common carp, roach and pumpkinseed). A significant negative impact of Flix reservoir on condition (eviscerated and liver weights, adjusted for fish size with analysis of covariance) and reproductive traits (gonadal weight and number of mature eggs, adjusted for fish size) was also detected for several fish species. The responses to the pollutants were species-specific, and common carp (Cyprinus carpio) was the species with the clearest effects on fitness-related traits at the impacted area, despite also being among the most tolerant to pollution.

The potential ecological hazard of metals in soils may be measured directly using a combination of chemical and biological techniques or estimated using appropriate ecological models. Terrestrial ecotoxicity testing has gained scientific credibility and growing regulatory interest; however, toxicity of metals has often been tested in freshly amended soils. Such an approach may lead to derivation of erroneous toxicity values (EC₅₀) and thresholds. In this study, the impact of metal amendments on soil ecotoxicity testing within a context of ion competition was investigated. Four coarse-textured soils were amended with copper (Cu) and nickel (Ni), incubated for 16 weeks and conditioned by a series of total pore water replacements. RhizonTM extracted pore water Cu, Ni, pH and dissolved organic carbon (DOC) concentrations were measured after each replacement. Changes in ecotoxicity of soil solutions were also monitored using a lux-based biosensor (Escherichia coli HB101 pUCD607) and linked to variations in soil solution metal and DOC concentrations, pH and selected characteristics of the experimental soils (exchangeable calcium (Ca) and magnesium (Mg)). Prior to conditioning of soils, strong proton competition produced relatively high EC₅₀ values (low toxicity) for both, Cu and Ni. The successive replacement of pore waters lead to a decline of labile pools of metals, DOC and alleviated the ecotoxicological protective effect of amendment impacted soil solution chemistry. Consequently, derived ecotoxicity values and toxicity thresholds were more reflective of genuine environmental conditions and the relationships observed more consistent with trends reported in historically contaminated soils.

This study was carried out to assess the overall water quality and identify major variables affecting the deep groundwater quality in Kathmandu Valley, Nepal. Forty-two deep wells were sampled during premonsoon and monsoon seasons in 2007 and analyzed for the major physicochemical variables. The water quality variables such as NH ₄ ⁺ -N, Fe, Pb, As, and Cd at most of the sampling locations exceeded the World Health Organization guideline levels for drinking water. Multivariate statistical techniques such as factor analysis and cluster analysis were applied to identify the major factors (variables) corresponding to the different source of variation in deep groundwater quality. Factor analysis indentified six major factors explaining 74.77% of the total variance in water quality; and the major variations are related with the degree of groundwater mineralization, decomposition of organic matter, and reduction of groundwater environment. The water quality of deep groundwater is influenced by the natural hydrogeochemical environment. The wells are broadly divided into two major groups based on the similar groundwater characteristics using cluster analysis. Results show that water quality of deep groundwater does not vary significantly as a function of season.

The objective of this paper is to design a pilot plant electrochemical reactor and to prove the operational concept of the electrochemical production of ferrate in situ and its online application for sewage treatment. To that end, the first part of this paper focuses on the analysis of the main engineering aspects of the reactor and the electrochemical process that affect the ferrate production, using laboratory scale experiments such as the interelectrode gap, the space-time yield, the area/volume (A/V) ratio, the current efficiency, and the energy consumption. The second part focuses on the production of ferrate using a pilot plant scale to prove the operational concept of the electrochemical generation of ferrate in situ and its online application as a step towards its full scale application for water and wastewater treatment.

The current study investigated the sorption of sulfadimethoxine (SMT), sulfamethoxazole (SMX), tetracycline (TET), and oxytetracycline (OTC) to Na-rich montmorillonite clay in synthetic effluent (SE) and field wastewater effluent (FE). Both SMT and SMX showed a low sorption capacity and are therefore likely to be highly mobile in the environment, while the sorption of TET to clay in environmental pH range (6.5-7.5) showed similarly high adsorption capacity. Differences in sorption capacities of TET and OTC to SE or FE were attributed to the various concentrations of divalent cations in the effluents. In addition, differences in sorption of OTC or TET to SE were attributed to their different molecular structure. Moreover, the adsorption of TET in SE and FE showed linear adsorption isotherms and fitted to Freundlich model. Further experiments showed that addition of humic acid or SE to TET sorbed to clay did not enhance or suppress the sorption of TET to clay.

The capacity of microalgae to accumulate heavy metals has been widely investigated for its potential applications in wastewater (bio)treatment. In this study, the ability of Desmodesmus pleiomorphus (strain L), a wild strain isolated from a polluted environment, to remove Cd from aqueous solutions was studied, by exposing its biomass to several Cd concentrations. Removal from solution reached a maximum of 61.2 mg Cd g⁻¹ biomass by 1 day, at the highest initial supernatant concentration used (i.e., 5.0 mg Cd L⁻¹), with most metal being adsorbed onto the cell surface. Metal removal by D. pleiomorphus (strain ACOI 561), a commercially available ecotype, was also assessed for comparative purposes; a removal of 76.4 mg Cd g⁻¹ biomass was attained by 1 day for the same initial metal concentration. Assays for metal removal using thermally inactivated cells were also performed; the maximum removal extent observed was 47.1 mg Cd g⁻¹ biomass, at the initial concentration of 5 mg Cd L⁻¹. In experiments conducted at various pH values, the highest removal was achieved at pH 4.0. Both microalga strains proved their feasibility as biotechnological tools to remove Cd from aqueous solution.

Peroxidase from fenugreek (Trigonella foenum-graecum) seeds was highly effective in the decolorization of textile effluent. Effluent was recalcitrant to the action of fenugreek seeds peroxidase (FSP). However, in order to effectively decolorize effluent by peroxidase, the role of six redox mediators has been investigated. The maximum decolorization of textile effluent was observed in the presence of 1.0 mM 1-hydroxybenzotrizole, 0.7 mM H₂O₂, and 0.4 U ml⁻¹ of FSP in the buffer of pH 5.0 at 40°C in 2.5 h. The decolorization of textile effluent in a batch process by peroxidase was 85% in 5 h, whereas the complete decolorization of textile effluent by membrane-entrapped FSP was observed within 11 h of its operation. The absorption spectra of treated effluent exhibited a marked diminution in the absorbance at different wavelengths compared to untreated effluent.

This study assesses the effect of salinity in bioavailability and toxicity of Zn by means of laboratory bioassays by observing contamination in both sediment and water, accumulation of Zn in biological tissues, and histopathological damage in the gills and guts tissues of Ruditapes philippinarum clams, which were exposed to different types of sediments from the Gulf of Cádiz (SW Spain) as well as two dilutions of toxic mud coming from an accidental mining spill. With this objective, the coefficients of distribution (K D) for Zn between overlying water and sediments were calculated, the histopathological frequencies in the tissues of the gills and guts of clams were determined, and the biota-sediment bioaccumulation factors as well as the bioaccumulation factors were quantified in the different stations. Results showed that the greatest histopathological damages appeared when the salinity values decreased. Statistical results showed that salinity was inversely correlated with histopathological damage (p < 0.01) for the lesion index for gills. The most outstanding results were observed in the two dilutions of toxic mud (0.3% and 7.9%) at a salinity value of 10. Salinity was inversely correlated with the concentration of Zn in biological tissues (p < 0.05) and inversely correlated with the concentration of Zn in water and sediment. Zn mobilization to the overlying water is produced when salinity values decrease.

Micellar-enhanced ultrafiltration (MEUF) is an effective separation technique for removing metal ions from aqueous environments. The critical micellar concentration (CMC) of two anionic surfactants, sodium dodecyl sulfate (SDS) and linear alkylbenzene sulfonate (LAS), was determined by means of conductometry. The effects of pH, conductivity, and surfactant concentration on the permeate flow, retention of surfactants and nickel by MEUF, was studied. Results showed that for surfactant concentrations beyond the CMC, Ni(II) retention with SDS was slightly higher than with LAS (S/M = 45: Ni(II) retention was 70% and 55% for SDS and LAS, respectively). LAS surfactant was always retained in higher quantities than SDS. An increase in conductivity produced large reduction in Ni(II) retention and slightly increased surfactant retention. pH values between 4 and 8 did not affect nickel retention but enhanced the SDS and LAS surfactant retentions.