This study assessed potential bioaccumulation of various trace elements in grasses and earthworms as a consequence of soil incorporation of organic amendments for in situ remediation of an orchard field soil contaminated with organochlorine and Pb pesticide residues. In this experiment, four organic amendments of differing total organic carbon content and quality (two types of composted manure, composted biosolids, and biochar) were added to a contaminated orchard field soil, planted with two types of grasses, and tested for their ability to reduce bioaccumulation of organochlorine pesticides and metals in earthworms. The experiment was carried out in 4-L soil microcosms in a controlled environment for 90 days. After 45 days of orchardgrass or perennial ryegrass growth, Lumbricus terrestris L. were introduced to the microcosms and exposed to the experimental soils for 45 days before the experiment was ended. Total trace element concentrations in the added organic amendments were below recommended safe levels and their phytoavailablity and earthworm availability remained low during a 90-day bioremediation study. At the end of the experiment, total tissue concentrations of Cu, Cd, Mn, Pb, and Zn in earthworms and grasses were below recommended safe levels. Total concentrations of Pb in test soil were similar to maximum background levels of Pb recorded in soils in the Eastern USA (100 mg kg⁻¹ d.w.) because of previous application of orchard pesticides. Addition of aged dairy manure compost and presence of grasses was effective in reducing the accumulation of soil-derived Pb in earthworms, thus reducing the risk of soil Pb entry into wildlife food chains.

The olive oil industry produces a highly complex wastewater, known as olive oil mill wastewater (OOMW), which represents a relevant environmental problem for the Mediterranean region. Several physicochemical, biological and combined treatments have been tested to deal with this industrial externality but none was totally effective in reducing its toxicity for species inhabiting the receiving freshwater systems. Within this framework, nanotechnology appears as a promising research area, offering new approaches for the treatment of wastewaters based on the enhanced physical and chemical properties of nanomaterials (NMs). In this context, this work aimed to investigate the treatability of OOMW through several treatments involving advanced oxidation processes plus the use of two nanomaterials as catalysts (UV/H₂O₂, UV/TiO₂, UV/Fe₂O₃, UV/TiO₂/H₂O₂ and UV/Fe₂O₃/H₂O₂). The concentrations of the catalyst and of the oxidant agent were also investigated. The results obtained showed that photodegradation treatments combining TiO₂ or Fe₂O₃ NMs with H₂O₂ were the most efficient. Regarding the OOMW toxicity to Vibrio fischeri, it was significantly reduced with the following treatments: UV/TiO₂/H₂O₂ and UV/Fe₂O₃/H₂O₂. However, the highest reduction recorded for this parameter was obtained in the treatment with UV/H₂O₂. The use of NMs combined with H₂O₂ showed a great potential for removing phenols from OOMW, which have been pointed out as the major toxic compounds of this wastewater.

Cr(VI) adsorption onto a novel fibrous ethylenediamine-functionalized polyethylene/polypropylene (PE/PP-g-PGMA-EDA) nonwoven fabric was investigated in aqueous solutions. The ethylenediamine functionalities were immobilized on the PE/PP nonwoven fabric through the epoxy groups of poly(glycidyl methacrylate) (PGMA) grafted to the fibers via radiation-induced emulsion graft polymerization in aqueous solution. Optimum conditions for grafting and subsequent modification steps were determined. The adsorbents were characterized by FTIR, XPS, and SEM techniques. Cr(VI) adsorption was studied in batch mode as a function of pH, feed concentration, contact time, ionic strength, and coexisting anions. The nonwoven adsorbent exhibited efficient, rapid Cr(VI) removal; high adsorption capacity; and insignificant interference from coexisting ions. Adsorbed Cr(VI) ions were desorbed using 2 M HNO₃ solution, and the adsorption capacity of the nonwoven fabric was retained for four adsorption–desorption cycles. The data for Cr(VI) adsorption on the nonwoven fabric fitted to the Langmuir isotherm model well. The maximum adsorption capacity for the Langmuir isotherm was 178.9 mg Cr(VI)/g polymer at pH 3.00. Graphical Abstract ᅟ

An in situ post tsunami study was conducted to assess the effect of water management and rainfalls in soil properties and water quality at a low-lying coastal area of central Chile affected by Mw8.8 Earthquake Tsunami the night of 27 February 2010. Soil samples were taken at two depths (0 to 20 and 20 to 40 cm) during 2010 and late 2012. Water quality in a local shallow well was also monitored in 2010 and 2012. High soil salinity was recorded 2 months later than tsunami occurs, closely associated to water-soluble chloride and cations (Cl⁻ > > Na⁺ > > Ca²⁺ > Mg²⁺ > K⁺), ionic toxicities, and vegetal inhibition (Vasconcellea pubescens) by less available water to plants. An initial reduction in soil pH due to ionic strength and coarse-textured class of soil was observed and the sodium adsorption ratio (SAR) in soil varied between 5.7 and 11.2 (mmol L⁻¹)⁰.⁵ showing to be saline. Although SARw values are very high (>18 (mmol L⁻¹)⁰.⁵), it does not exist risks of reduction on soil infiltration rates according to ECw (>5 dS m⁻¹) obtained. After 2 years, soil salinity was drastically reduced in the affected areas due to high soil permeability and natural attenuation (rainfalls and leaching effects), with sulfate and bicarbonate concentrations showing excessive values. Further, irrigation water quality returned to pre-tsunami situation, with only levels of sodium slightly exceeding desirable range from health point of view. Finally, it is suggested a proper design of irrigation systems before implementing other management practices.

Along the southeastern coast of Costa Rica, a variety of pesticides are intensively applied to produce export-quality plantains and bananas. In this region, and in other agricultural areas, fish kills are often documented by local residents and/or in the national news. This study examines principal exposure pathways, measured environmental concentrations, and selected toxicity thresholds of the three most prevalent pesticides (chlorpyrifos, terbufos, and difenoconazole) to construct a deterministic risk assessment for fish mortality. Comparisons of observed pesticide concentrations, along with estimated biological effects and observations during actual fish kills, highlight gaps in knowledge in correlating pesticide environmental concentration and toxicity in tropical environments. Observations of fish kill events and measured pesticide concentrations in the field, along with other water quality indicators, suggest that a number of environmental conditions can interact to cause fish mortality and that current species toxicity datasets may not be applicable for estimating toxicological or other synergistic effects, especially in tropical environments.

The capacities of a biosurfactant producing and polycyclic aromatic hydrocarbon (PAH) utilizing bacterium, namely, strain 1C, isolated from an Algerian contaminated soil, were investigated. Strain 1C belonged to the Paenibacillus genus and was closely related to the specie Paenibacillus popilliae, with 16S rRNA gene sequence similarity of 98.4 %. It was able to produce biosurfactant using olive oil as substrate. The biosurfactant production was shown by surface tension (32.6 mN/m) after 24 h of incubation at 45 °C and 150 rpm. The biosurfactant(s) retained its properties during exposure to elevated temperatures (70 °C), relatively high salinity (20 % NaCl), and a wide range of pH values (2–10). The infrared spectroscopy (FTIR) revealed that its chemical structure belonged to lipopeptide class. The critical micelle concentration (CMC) of this biosurfactant was about 0.5 g/l with 29.4 mN/m. In addition, the surface active compound(s) produced by strain 1C enhanced PAH solubility and showed a significant antimicrobial activity against pathogens. In addition to its biosurfactant production, strain 1C was shown to be able to utilize PAHs as the sole carbon and energy sources. Strain 1C as hydrocarbonoclastic bacteria and its interesting surface active agent may be used for cleaning the environments polluted with polyaromatic hydrocarbons.

Textile dyes and antibiotics are two main classes of environmental pollutants which could be found in soil and water. Those persistent pollutants can have a negative influence on plant growth and development and affect the level of secondary metabolites. In the present work, we studied the effect of textile dyes and antibiotics on total leaf flavonoid contents in wheat (Triticum aestivum L.). Contaminant solutions were applied daily using concentrations of 0.5 mg L⁻¹ (lower) and 1.5 mg L⁻¹ (higher dose) for either 1 or 2 weeks. We observed that exposure to the higher concentration of textile dyes resulted in a reduction in flavonoid content while antibiotics enhanced flavonoid contents at lower doses of exposure and reduced at higher doses of exposure. These results suggest that diffuse chronic pollution by artificial organic contaminants can importantly alter antioxidative capacity of plants.

Inorganic arsenic occurs mainly in As(III) and As(V) states in water environment, but arsenite is more toxic and difficult to remove than arsenate by usual adsorption processes. To achieve the in situ oxidation of As(III) and simultaneous removal of both As(III) and As(V) in water, a novel-layered double hydroxide (Mg–Fe–S₂O₈–LDH) with the intercalation of persulfate has been designed and synthesized by a calcination-reconstruction method. The arsenic adsorption performances and removal mechanism with the Mg–Fe–S₂O₈–LDH material were studied. The experimental result showed that, since the strong oxidation ability of the exchangeable persulfate ions from the LDH, the As(III) species in water were almost completely oxidized to the As(V) state and simultaneously adsorbed onto the Mg–Fe–S₂O₈–LDH. It was found that the maximum adsorption capacity for As(III) and As(V) in single-pollutant system was 75.00 and 75.63 mg·g⁻¹, respectively. When the adsorbent dosage was 0.5 g·L⁻¹ for a mixed As(III) and As(V) solution, the batch experiment showed that the residual arsenic concentration can be reduced from 1 mg·L⁻¹ to lower than the limit value of drinking water standard recommended by WHO. It indicated that the synthesized Mg–Fe–S₂O₈–LDH is a potential attractive adsorbent for simultaneous removal of As(III) and As(V) in water.

The present study reports the synthesis and characterization of metallic nanoparticles (NPs) of Pd and bimetallic alloys of PdCu NPs for their application as catalysts to achieve the microbial reduction of p-nitrophenol (PNP). Addition of bimetallic alloys of PdCu NPs to methanogenic sludge incubations increased up to threefold the rate of reduction of PNP. Moreover, their presence promoted a more efficient and selective reduction of PNP to the desired product (p-aminophenol) with negligible accumulation of toxic intermediates (p-nitroso-phenol and p-hydroxylamine-phenol), which prevailed in sludge incubations lacking nanocatalysts. PdCu NPs synthesized by adding precursors H₂PdCl₄ and H₂CuCl₄ independently and simultaneously to the synthesis vessel showed superior catalytic properties as compared to those produced by mixing the same precursors prior addition to the synthesis vessel. The enhanced catalytic properties of bimetallic NPs could be explained by higher physical stability and interfacial arrangement within PdCu alloys promoting a more efficient transfer of reducing equivalents derived from lactate/ethanol fermentation towards the target nitro group in PNP. A wastewater treatment technology, combining the microbial activity of methanogenic consortia and the catalytic activity of bimetallic NPs, is proposed as an alternative for the removal of recalcitrant pollutants from wastewaters.

A macroporous glycidyl methacrylate (GMA)–methylmethacrylate (MMA)–divinyl benzene (DVB) terpolymer functionalized with diethylenetriamine tetraacetic acid (DTTA) (GMA-MMA-DVB-DTTA) sorbent was successfully applied for the uptake of Cu(II) from the aqueous solutions. Adsorption characteristics for copper ion were investigated by a batch sorption in under different experimental conditions, and the optimum parameters for the quantitative sorption of Cu(II) ion were found to be as follows: pH of 7.0, a contact time of 30.0 min, and a sorbent amount/solution volume ratio of 1.5 mg/mL. The quantitative elution from the sorbent was performed with 1.0 M HCl (>95 %). Among three kinetic models, the pseudo-second-order kinetic model provides the best correlation for the process. The nonlinear resolution of the Langmuir isotherm equation has been found to show the closest fit to the equilibrium data. The results indicates that the presence of the competitor ions (Al, Ba, Co, Mn, Mg, and Ni) has no obvious influence on the sorption of Cu(II) ion under the optimum conditions and the polymeric sorbent has a good selectivity for the sorption of Cu(II) ions with a sorption percent of ≥99 %. Sorption/desorption studies were performed for ultrapure, tap, bottled drinking and industrial wastewater samples, and it is examined that the proposed method has been successfully applied to the real samples for the removal of Cu(II) acceptable accuracy and precision. The results of this work indicated that the polymeric sorbent could be a simple and suitable method for the effective removal of Cu(II) ions from waters.