The volatile monoterpene alpha-pinene has been measured in sediments of a selected area at "Carlos Anwandter" Nature Sanctuary, a Ramsar protected wetland located at the northwest of Valdivia City, south-central Chile. The ecosystem was seriously damaged by an uncontrolled liquid emission of a pulp mill (CELCO-Arauco) located about 15 km upstream of Rio Cruces during 2004. Exploratory data analysis was applied to analytical data collected from sediment samples, having found alpha-pinene as a reiterative chemical at relatively high concentrations in some specific areas of the wetland. The decrease of the total concentration of alpha-pinene in the area under study is coincident with a point contamination that occurred during 2004 (12,240 ng g(-1)) showing a decay in 2005 (7,890 ng g(-1)) and middle of 2006 (4,060 ng g(-1)). The following years, last 2006, 2008, and 2009, show a relatively constant concentration with a clear tendency toward baseline levels (2,460-2,640 ng g(-1)). Since the decrease of concentrations of alpha-pinene in sediments in the period 2004-2009 shows an opposite trend as compared to the surface area increase of pine and eucalyptus plantation in Region de Los Rios, and not having found potential sources of alpha-pinene by anthropogenic activities other than the pulp mill in the area under study, it may be finally concluded that this compound did not enter the bodies of water from a gradual and natural process; instead there is a base to sustain anthropogenic input. alpha-Pinene in sediments may be a plausible chemical tracer capable of detecting pollution events over time and its impacts in aquatic ecosystems as well as changes in aquatic ecosystems produced by improperly treated pulp mill liquid emissions that use pine and eucalyptus species.

The effectiveness of activated carbon sample (Carbonₑₓₚ) prepared by KOH chemical activation in hampering oligomerization of multicomponent adsorption was systematically examined. Anoxic (absence of molecular oxygen) and oxic (presence of molecular oxygen) adsorption isotherms of single-solute (2,4-dimethylphenol), binary solute (2-methylphenol/2,4-dimethylphenol), and ternary solute (phenol/2-methylphenol/2,4-dimethylphenol) were studied, using Carbonₑₓₚ and commercial granular activated carbon F400. Both binary solute adsorption and ternary solute adsorption on Carbonₑₓₚ indicated no impact of the presence of molecular oxygen on the adsorptive capacity. No significant differences between oxic and anoxic environment were noticed for any multicomponent adsorption systems, which indicated the effectiveness of Carbonₑₓₚ in hampering the oligomerization of phenolic compounds. On the other hand, in F400, which has lower microporosity and acidic functional groups, significant increases in the adsorptive capacity had been observed when molecular oxygen was present.

Heavy metals occur naturally in soil, at concentrations that depend on the parent material from which the soil was formed, the processes of formation, and the composition and the proportion of the components of its solid phase. Quantifying these concentrations is important for environmental studies of soil contamination and pollution, and choosing the methods for doing so is a key step in establishing heavy metal contents in soil samples. We evaluated two digestion methods (aqua regia and EPA 3051, both microwave oven-assisted) for assessing pseudo-total concentrations of Cd, Co, Cr, Cu, Ni, Pb and Zn in the surface layer (0–20 cm) of soil samples from the Brazilian agricultural frontier in the southwestern Amazon. Nineteen composite samples of the most representative soil classes for the states of Mato Grosso and Rondônia were collected under native vegetation undisturbed by human intervention. Canonical discriminant analysis and principal component analysis were used for multivariate exploration of the data. Aqua regia extracted higher amounts of Co, Ni, Pb, and Zn than EPA 3051, while levels of Cr and Cu did not differ between methods. In general, aqua regia recovered more of the metals when compared to reference soil samples.

With the constant development of new ionic liquids, the understanding of the chemical fate of these compounds also needs to be updated. To this effect, the interaction of a number of novel ionic liquids with soils was determined. Therefore, three novel headgroups (ammonium, phosphonium, or pyrrolidinium) with single or quaternary substitution were tested on a variety of soils with high-to-low organic matter content and high-to-low cation exchange capacity, thereby trying to capture the full range of possible soil interactions. It was found that the ionic liquids with single butyl alkyl chain interacted more strongly with the soils (especially with a higher cation exchange capacity), at lower concentrations, than the quad-substituted ionic liquids. However, the quad-substituted ionic liquids interacted more strongly at higher concentrations, due to the double-layer formation, and induced stronger dipole interaction with previously sorbed molecules.

Geochemical characterization of two landfills, one closed and the other still active, both located near Komotini (Thrace, Greece), has been carried out. The aim was to provide an integrated and reliable methodology for a rapid assessment of the real impact of a municipal solid waste landfill, in the main environmental matrices (air and water) of the surrounding areas. The chemical (CO₂, CH₄, CO, H₂, N₂, and O₂ + Ar) and isotopic characterization (δ¹³C₍CO₂₎ and δ¹³C₍CH₄₎) of landfill gas and chemical (Na⁺, K⁺, Ca²⁺, Mg²⁺, Cl⁻, SO₄ ²⁻, HCO₃ ⁻, NH₄ ⁺, NO₃ ⁻, NO₂ ⁻, B, COD, Fe, Mn, As, Cr, Ni, Cu, Zn, Cd, Pb, and Hg) and isotopic analysis (δD, δ¹⁸O, tritium content, and δ¹³CDIC) of leachate, stream waters and groundwaters, and flux survey on the air–soil interface has been carried out. Combined chemical and isotopic analysis of the fluids collected inside and in the surroundings of the Komotini landfills supply a detailed picture of biogas emission and composition as well as of leachate chemistry and interaction with local waters. The results arising in this case study demonstrate that it is possible to propose a quick and reliable geochemical protocol to get a detailed picture of the state of health of the environment around a landfill.

A neutrophilic, autotrophic bacterium that couples iron oxidation to nitrate reduction (iron-oxidizing bacteria [IOB]) under anoxic conditions was isolated from a working bioremediation site in Trail, British Columbia. The site was designed and developed primarily to treat high concentrations of Zn and As that originate from capped industrial landfill sites. The system consisted of two upflow biochemical reactor cells (BCR) followed by three vegetated wetland polishing cells with sub-surface flow and a holding pond. During a 5-year period (2003–2007), the system treated more than 19,100 m³ of contaminated water, removing and sequestering more than 10,700 kg of As, Zn and sulfate at average input water concentrations of: As, 58.6 mg l⁻¹ (±39.9 mg l⁻¹); Zn, 51.9 mg l⁻¹ (±35.4 mg l⁻¹) and SO₄ ²⁻, 781.5 mg l⁻¹ (±287.8 mg l⁻¹). The bacterium was isolated in order to better understand the mechanisms underlying the consistent As removal that took place in the system. Analysis using Basic Local Alignment Search Tool (BLAST) database showed that the closest homologies are to Candidatus accumulibacterphosphatis (95 % homology), Dechloromonas aromatica (94 %), and Sideroxydans lithotrophicus ES-1 (92 %) Within the BCR cells, the IOB oxidized Fe²⁺ generated by iron-reducing bacteria (IRB); the source of the iron was most likely biosolids and coatings of iron oxide on locally available sand used in the matrix. We have provisionally designated the novel bacterium as TR1.

Aquatic birds are often used as a health indicator of the marine ecosystem. African penguins living in the zoo make good research material as they form a link between the marine and the terrestrial ecosystem in terms of xenobiotic circulation. Tests were performed on whole herring—the food of the penguins—as well as on bird muscle, liver, brain, eggs, feathers and guano in order to determine total mercury, aldrin, dieldrin, endrin, isodrin, endosulfan isomers, endosulfan sulfate, methoxychlor, dichlorodiphenyltrichloroethane (DDT) and its metabolites. In herring and penguin, the tests did not show the presence of β-endosulfan, endosulfan sulfate, aldrin and isodrin. It was shown that penguins absorb about 36.8 μg of organochlorine pesticides and 4.6 μg of mercury with their food on a daily basis. Xenobiotics accumulate mostly in the liver, from where they are transported to the muscles and the brain, where the highest bioaccumulation factor is reached by endrin and pp’-DDT. Conceivably, the older the penguin, the higher is the concentration level of pesticides in its liver and brain. Molting was found to be the most effective way of eliminating mercury, dieldrin and methoxychlor from the system. Insecticides, such as DDT and its metabolites, were removed most effectively by females through laying of eggs. The standard four eggs laid within a year may have contained up to 20 % of the total amount of pesticides which had been absorbed with food, but no more than 5 % of mercury.

Recently, metal nanoparticles have attracted attention as promising peroxygen activators for the rapid and effective remediation of organic contaminants. In this work, a one-dimensional physical model experiment was designed to investigate the mobility of the metal nanoparticles in porous media and the potential use of metal nanoparticles as peroxygen activators for in situ treatment of source zones. We found that our synthesized nano-Pd-Fe0 particles were mobile in a non-geological porous medium and relatively immobile in a geological porous medium. In addition, we observed that iron-based bimetallic nanoparticles were able to remain in suspension in an ideal aqueous system much longer (>6 weeks) than iron-based monometallic nanoparticles (<1 h). To overcome the nano-Pd-Fe0 particle delivery issue in geological porous media, an activation zone approach was adopted. Nano-Pd-Fe0 particles were injected in order to create a zone to activate persulfate for the treatment of a trichloroethylene source zone. Trichloroethylene mass destruction was only 9 % higher in the nano-Pd-Fe 0 activated persulfate system compared to the non-activated persulfate system as revealed by a short-duration chloride concentration spike in the effluent. In addition, the nano-Pd-Fe0 activation zone was rapidly deactivated after being exposed to persulfate as visually observed by a color change, indicating that the longevity of the activation zone is limited. © 2013 Springer Science+Business Media Dordrecht.

The sorption behaviors of brilliant blue FCF dye by natural clay and modified with iron chloride were determined. The materials were characterized by X-ray diffraction and scanning electron microscopy, and the zero point charges were also determined. The effects of pH, contact time, dye concentration, and temperature were considered. The results showed that clay does not suffer any important change in its structure after the chemical treatments. The pH influences the sorption of the dye in the unmodified clay, but this effect was not observed in the iron-modified clay. The equilibrium time and the sorption capacity for the unmodified clay were 48 h and 6.16 mg/g, while for the iron-modified clay, 24 h and 14.22 mg/g, respectively. The sorption kinetics results were best adjusted to the pseudo-first-order and pseudo-second-order models. Sorption isotherms were best adjusted to the Langmuir model, indicating that both clays have a homogeneous surface. Thermodynamic parameters (E, ΔS, ΔG and ΔH) were calculated for the natural clay from the data of the sorption kinetics at temperatures between 20 and 50 °C, indicating that the sorption process is exothermic. For the case of the iron-modified clay, it was not possible to calculate these thermodynamic parameters because the sorption capacities were similar in the temperature range selected.

A study was undertaken to assess the extent of mercury contamination in the water and sediment in a seasonal wetland, as well as to determine the relationship between environmental parameters and the distribution of the mercury contamination. Water and sediment samples were collected and analysed for methylmercury, inorganic mercury and other physical and chemical variables. One-way analysis of variance and homogeneity of variance were performed, and linear regression analysis was used to determine correlations between mercury and other environmental variables. The highest mercury concentrations were recorded at the sites located closest to the industrial complex. Methylmercury concentrations in the water and sediment were mostly higher during the low flow season, while inorganic mercury concentrations in the water and sediment were higher during the high flow and low flow seasons, respectively. Chromium, manganese, organic carbon and fine sediment particles were found to have significantly positive correlations with mercury concentrations in water and sediment. It was also found that the mercury concentrations decreased within a relatively short distance from the sites closer to the industrial complex to the sites further downstream.