Contaminant elution and tracer (CET) tests are one method for characterizing the impact of mass transfer, transformation, and other attenuation processes on contaminant transport and mass removal for subsurface systems. The purpose of the work reported herein is to explore specific well-field configurations for improving CET tests by reducing the influence of preferential flow and surrounding plume effects. Three injection-extraction well configurations were tested for different domain conditions using a three-dimensional numerical model. The three configurations were the traditional configuration with a single pair of injection-extraction wells, modified configuration I with one extraction well located between two injection wells, and modified configuration II with two pairs of injection-extraction couplets (one nested within the other). Elution curves for resident contaminant and breakthrough curves from simulated tracer tests were examined for specific landmarks such as the presence and extent of steady state (relatively high concentrations) and asymptotic (asymptotic decrease to low concentrations) phases, as well as distinct changes in slope. Temporal moment analysis of the breakthrough curves was conducted to evaluate mass recovery. Effective diffusion coefficients were obtained by fitting selected functions to the elution curves. Based on simulation results for a homogeneous domain, full isolation of the inner extraction well from the surrounding plume was obtained for the modified configuration II, whereas the extraction wells are impacted by the surrounding plume for the other two configurations. Therefore, configuration II was used for additional simulations conducted with layered and heterogeneous domains. Tracer test simulations for homogeneous and layered domains indicate 100% mass recovery for the inner extraction well. For the heterogeneous domain, decreasing the distance between the inner injection-extraction well couplet and adjusting the pumping rate distribution between the two extraction wells increased the mass recovery from 69 to 99%.

Currently, the use of nanotechnologies is in rapid expansion, which entails increasing risks of environmental contamination by nanoparticles. Many studies describe the toxic effects on human cells, but little is known about the possible adverse effects on plants. Currently, various nanoparticles are often detected in streams, wastewater, and sewage due to widespread nanoparticle uses. We studied the accumulation and the effect of metal oxide nanoparticles together with their bulk counter particles and soluble metal salts on the growth of a wetland plant species true fox-sedge (Carex vulpina L.). The concentration 100 mg/l of copper nanoparticles significantly affected the growth of the plants, roots characteristics, and content of the photosynthetic pigments in leaves, while the same concentration of iron nanoparticles did not reduced any of the measured items. Using the bulk materials, the effect was very similar.

Oil spills might lead to severe environmental impacts to the affected fauna, disrupting local food webs, and causing mass mortality in many species. However, little is known about long-term impacts of oil spills, or even if such impacts can be detectable after several generations. In this study, we investigate the genetic variability of three freshwater species—Mimagoniates microlepis (Characiformes: Characidae), Scleromystax barbatus (Siluriformes: Callichthyidae), and Phalloceros harpagos (Cyprinodontiformes: Poeciliidae)—in rivers that were affected by a large oil spill in the state of Paraná, southern Brazil, on February of 2001. Samples were obtained from nine different locations, such that rivers that were directly affected by the oil spill could be compared with similar rivers in the same region that were unaffected. A fragment of the cytochrome C oxidase subunit I mitochondrial gene was sequenced from each specimen, and the level of genetic variability was assessed. Based on estimates of haplotype and nucleotide diversity, no impact of the oil spill could be detected in impacted rivers. These results suggest that fish populations in the region showed resilience to the pollutant, such that immigration from other locations was able to reestablish levels of genetic variability comparable to those of unimpacted rivers.

Until recently, there have been only few published reports concerning the use of mangrove macroalgae as biomonitors to assess the estuarine metal contamination. Therefore, the present study was an effort to investigate the biomonitoring of metal contamination using mangrove macroalgae in the tropical Miri estuary of Sarawak, Malaysia. The metal concentrations (Cu, Fe, Mn, and Zn) were determined in the surface sediments, estuarine water, and six dominant macroalgae species that epiphytically grow on mangrove pneumatophores. The results showed that the scheme of metal occurrences in estuarine surface water and sediments was Fe > Mn > Zn > Cu and Fe > Zn > Mn > Cu, respectively. Among the studied metals in algal tissues, irrespective of macroalgal species, the concentration of Fe was found to be the highest. Significant positive correlations were found between Cu and Zn in all macroalgal species (except Caloglossa ogasawaraensis and Dictyota sp.), indicating the common origin of those elements. Concentrations of each of the studied metal in algal tissues varied among macroalgal species, probably because of the differences of structure, age, and growth of thallus among macroalgal species. To our knowledge, this is the first comprehensive report describing the biomonitoring of metal contamination using macroalgae from Malaysian mangrove systems.

Sediments deposited on road surfaces are contaminated with pollutants; the load of pollution increases from coarse to fine particles. When it rains, different fractions of the road-deposited sediments are washed off depending on the rain intensity, the slope of the catchment, and other site-specific factors. This road runoff is often treated using settling processes implemented in different types of manufactured treatment devices. These devices can be tested with well-defined artificial test materials to determine the removal efficiencies of particulate matter in a reproducible manner. However, the suitability of the currently deployed artificial test materials to represent the settling behavior of real runoff particle collectives is largely unknown. In this study, a laboratory method to measure and compare the settling behavior of artificial and real particle collectives with a reproducible particle size composition was developed. The particle collectives were obtained from different road surfaces, fractionated into sieve classes, and then recomposed into a defined particle size distribution that represented the road runoff. The settling velocity was analyzed in a modified settling column setup under constant conditions. The resulting data form a cumulative curve of the settling velocities for both artificial and real particle collectives. The main result from this work is that the tested artificial material and the recomposed real particle collectives have comparable settling behaviors despite different losses on ignition and densities.

Chemical inputs from agricultural activities represent a threat to aquatic biota and its biochemical systems. Among these systems, acid phosphatases are involved in autophagic digestive processes, decomposing organic phosphates, signaling pathways, and other metabolic routes. In vitro tests are helpful to generate hypotheses about pollutant mechanisms of action through comparison of the toxicity effects of these compounds. In this work, we investigated the inhibitory effects of four organic pesticides and three metals on the acid phosphatases extracted from the freshwater microcrustacean Daphnia similis and the fish Metynnis argenteus. Our results demonstrated that only the metals have considerable inhibitory effects (50% or higher) on the enzyme activities. The calculated median effect concentrations (IC50) for the enzyme inhibition were 0.139 mM Hg²⁺ (fish enzyme), 0.652 mM Cu²⁺ (fish enzyme), and 1.974 mM Al³⁺ (Daphnia enzyme). Due to the relatively low value of the inhibition parameter for Hg²⁺, its inhibitory property could be used as a tool for Hg²⁺ detection in environmental samples. The enzyme activities obtained in the presence of the inhibitors are potential data as in vivo biomarkers for metals in both aquatic species.

The goal of this research was the electrooxidation (EO) of a nonionic surfactant nonylphenol decaethoxylate (NP-10) in aqueous solution and denim wastewater. Three different configuration systems were evaluated in batch cells using a boron-doped diamond (BDD) anode; copper, iron, and BDD were used as cathodes. The EO process was carried out in a batch process, in a glass cell with a capacity of 1000 mL. The anode surface area was 0.0307 m² and 1–3 A of current intensity were applied (3, 6, 10 mA/cm²) with an electrolysis time of 240 min for aqueous solution and 780 min for denim wastewater in order to investigate the degradation of the surfactant. The processes were analyzed in terms of chemical oxygen demand (COD) and total organic carbon (TOC). The maximum mineralization efficiency in aqueous solution for the BDD-Cu electrooxidation system was 92.2% for COD and 45.6% for TOC at pH 2 and 3 mA/cm² of current intensity. For denim wastewater, the removal efficiency was 44.1% for COD and 26.5% for TOC at pH 4.5 and 6 mA/cm² of current intensity, using a BDD-BDD system. The raw and treated (aqueous solution and denim) wastewater were characterized by UV-Vis and infrared spectroscopy.

Benzalkonium chloride (BAC) loaded to montmorillonites (Mt) or organomontmorillonites (OMt) generates a functional material that can be incorporated to several systems (polymers, paints, etc) as a controlled release bactericide. Understanding the BAC adsorption sites on these adsorbents is of high importance to clarify their adsorption/desorption characteristics in aqueous media or other solvents. In this work, a thorough study about the adsorption/desorption properties of Mt and OMt with regards to BAC is presented, in order to evaluate further BAC release with the consequent aquatic environment contamination. In this work, the BAC adsorption on two different sites is demonstrated: the interlayer space and the external surface. Depending on BAC concentration in water, sorption of BAC at Mt occurred in two steps. At adsorbed amount <0.5 mmol g⁻¹, there was an Mt interlayer expansion of 0.49 nm with no change of the external charge. At adsorbed amount >0.5 mmol g⁻¹, there was a new interlayer expansion attaining 0.75 nm and the external charge shifted to positive value. In the case of OMt, the introduction of BAC produced changes in the interlayer structure and in the external surface charge. BAC desorption was strongly dependent on the type of Mt or OMt and extraction solvent, knowledge of which will allow its safe use in environmental friendly technological applications.

Nitrogen dioxide (NO₂) is one of the major atmospheric pollutants, and the concentration of NO₂ is regarded as one of the indicators of air quality. In the past decades, China has experienced rapid economic growth and severe NO₂ pollution to match. We evaluate the trends and spatiotemporal patterns of tropospheric NO₂ over mainland China from 2005 to 2014 using vertical column density (VCD) datasets retrieved from the Ozone Monitoring Instrument (OMI). Results show that from 2005 to 2014, NO₂ pollution regions have enlarged at the national scale, and high NO₂ VCDs are mainly concentrated over highly populated regions in eastern China. The year 2011 is the turning point. Tropospheric NO₂ VCDs first significantly increase by 0.19 × 10¹⁵ molec cm⁻² year⁻¹ (R ² = 0.94, P = 0.002) from 2005 to 2011, and then decrease by 0.21 × 10¹⁵ molec cm⁻² year⁻¹ (R ² = 0.97, P = 0.016) from 2011 to 2014. Since 2011, tropospheric NO₂ VCDs over central-east China decrease remarkably. Tropospheric NO₂ VCDs is higher in November (3.630 × 10¹⁵ molec/cm²), December (4.758 × 10¹⁵ molec/cm²), and January (4.863 × 10¹⁵ molec/cm²), while lower in July (1.684 × 10¹⁵ molec/cm²), August (1.627 × 10¹⁵ molec/cm²), and September (1.703 × 10¹⁵ molec/cm²), indicating that winter and spring are the most polluted seasons. Due to the huge gap in population density and industry development between western and eastern China, the spatial pattern of tropospheric NO₂ VCDs shows large west-east difference.

Present study investigates the coagulation ability of Plantago ovata (P. ovata) seed extracts for turbidity removal. The active coagulant agents were successfully extracted from P. ovata seeds using different solvents such as distilled water (PO-DW), tap water (PO-TW), NaCl (PO-NaCl), and ammonium acetate (PO-AA). Experiments were conducted in batch mode for initial turbidity such as 500 NTU (high), 150 NTU (medium), and 50 NTU (low). Results demonstrated that P. ovata extracts are less efficient in low turbidities, while PO-NaCl was found to provide high coagulation activity in all initial turbidity concentrations compared to other extracts. PO-NaCl was able to remove 98.2, 94.9, and 80.2% of turbidity from water having in initial turbidities of 500, 150, and 50 NTU, respectively. Coagulation activity of the extract was the best when the extraction was performed for 50 min at room temperature. Jar test procedure with the coagulation time of 1 min and flocculation time of 30 min was optimized, irrespective of the initial turbidity. The optimum settling time for 500, 150, and 50 NTU water samples were 20, 30, and 90 min, respectively. PO-NaCl was used in different pH turbid solutions and it was found to be working very efficiently in alkaline conditions. The coagulation efficiency of the coagulant stored in refrigerator was higher than that stored at room temperature. Thus, the natural coagulants extracted from P. ovata seeds revealed to be effective for turbidity removal.