The well-known bacterium Sphingomonas wittichii RW1 catabolically degrades dibenzo-p-dioxin and dibenzofuran, as well as their chlorinated derivatives. The catabolic degradation of dioxin is initiated by a ring-hydroxylating dioxygenase. The biotransformation of carbazole by S. wittichii RW1 was determined in the present study. Dioxin dioxygenase from the dibenzofuran induced RW1 strain was thought to be unable to attack carbazole, which includes a heterocyclic aromatic dibenzopyrrole system. However, our results showed that carbazole was transformed to anthranilic acid and catechol. The color of the culture suspension changed upon addition of carbazole due to formation of a nitrogen-containing metabolite. Relevant metabolic intermediates were identified by gas chromatographic mass spectrometry and electrospray ionization time-of-flight mass spectrometry with comparison to the corresponding authentic compounds. The dioxygenase of the dibenzofuran induced RW1 attacked at the angular position adjacent to the nitrogen atom to give a dihydroxylated metabolic intermediate. Contrary to predictions made in previous reports, S. wittichii RW1 displayed positive catabolic activity toward carbazole.

To understand spatial and temporal variations of nitrous oxide (N₂O) fluxes, we chose to measure N₂O emissions from three plant stands (Kobresia tibetica, Carex muliensis, and Eleocharis valleculosa stands) in an open fen on the northeastern Qinghai–Tibetan plateau during the growing seasons from 2005 to 2007. The overall mean N₂O emission rate was about 0.018 ± 0.056 mg N m⁻² h⁻¹ during the growing seasons from 2005 to 2007, with highly spatiotemporal variations. The hummock (K. tibetica stand) emitted N₂O at the highest rate about 0.025 ± 0.051 mg N m⁻² h⁻¹, followed by the hollow stands: the E. valleculosa stand about 0.012 ± 0.046 mg N m⁻² h⁻¹ and the C. muliensis stand about 0.017 ± 0.068 mg N m⁻² h⁻¹. Within each stand, we also noted significant variations of N₂O emission. We also observed the significant seasonal and inter-annual variation of N₂O fluxes during the study period. The highest N₂O emission rate was all recorded in July or August in each year from 2005 to 2007. Compared with the mean value of 2005, we found the drought of 2006 significantly increased N₂O emissions by 104 times in the E. valleculosa stand, 45 times in K. tibetica stand, and 18 times in the C. muliensis stand. Though there was no significant relation between standing water depths and N₂O emissions, we still considered it related to the spatiotemporal dynamics of soil water regime under climate change.

The application of poly(acrylamide-co-sodium methacrylate) (AAm/SMA) hydrogel for the removal of Pb²⁺ ions from aqueous solutions has been investigated using batch adsorption technique. The extent of adsorption was investigated as a function of pH, adsorbent dose, and temperature. The Fourier transform infrared (FTIR) spectra showed that –NH₂ and –COOH groups are involved in Pb²⁺ ion adsorption. The obtained results were analyzed by pseudo-first-order, pseudo-second–order, and intraparticle diffusion models using both linear and nonlinear methods. It was found that the Pb²⁺ ion adsorption followed pseudo-first-order kinetics. Nonlinear regression analysis of six isotherms, Langmuir, Freundlich, Redlich-Peterson, Toth, Dubinin-Radushkevich, and Sips, have been applied to the sorption data, while the best interpretation was given by Redlich-Peterson. Based on the separation factor, R L, the Pb²⁺ ion adsorption is favorable, while the negative values of ∆G indicates that the Pb²⁺ ion adsorption on the investigated hydrogel is spontaneous.

Tributyltin (TBT) is a very effective biocide and an active ingredient in antifouling paints. Screening along the Indian coast yielded 49 bacterial isolates capable of TBT assimilation. The screening was done based on the ability of bacteria to grow in mineral salt medium (MSM) containing TBT as the sole source of carbon. All the isolates produced exopolysaccharides (biosurfactants) in the medium which aid in emulsification and thus ease bioavailability of TBT. Five isolates were identified as potent TBT degraders (namely, Pseudomonas pseudoalcaligenes, Pseudomonas stutzeri, Pseudomonas mendocina, Pseudomonas putida, and Pseudomonas balearica) based on their biomass production in MSM containing TBT as the sole source of carbon. In addition to evaluating the potential of individual bacterial strains, the study also focused on using a consortium of bacteria to explore their synergistic effect when grown on TBT. Further tests like growth profile, rhamnolipid secretion profile, extracellular protein secretion profile, and detection of siderophores were performed on these isolates when grown in MSM supplemented with 2 mM TBT concentration. Emulsification activity of the crude extracellular polysaccharides against kerosene was evaluated. It can be therefore inferred that TBT degradation by these marine pseudomonads is a two-step process: (a) dispersion of TBT in the aqueous phase and (b) tin–carbon bond cleavage by siderophores affecting debutylation of TBT. The consortium of bacteria may be effective in the treatment of TBT-contaminated waste water in dry docks.

The present work describes a detailed study about the adsorption of malachite green (MG) by a polyether-type polyurethane foam (PUF) using sodium dodecylsulfate (SDS) as a carrier. The adsorption process was based on the formation of a hydrophobic ionic-pair between the MG cationic dye and the dodecylsulfate anion, which presented high affinity for the PUF. The manifold employed in the study was built up by adjusting a cylinder of PUF with 200 mg in the arm of an overhead stirrer, which was soaked (and stirred) in the solution containing the dye and SDS. The adsorption process was characterized in relation to equilibrium and kinetic aspects. Langmuir (r 2 = 0.842) and Freundlich (r 2 = 0.996) isotherms were also employed for modeling the system as well as the Nernst partition law (r 2 = 0.999). A study about the recovery of MG and the PUF regeneration was conducted, and the acetonitrile was the most efficient solvent for the desorption of the adsorbed ionic pair. The obtained results showed that the concentration of SDS added to the medium plays an important role on the adsorption process, which can be better described by employing a second-order kinetic model.

An effective adsorbent for the removal of heavy metals was manufactured by immobilization of jujube powder. The adsorptions of Cd, Zn and Cu from aqueous solutions by jujube complex beads (Type 1 and Type 2) were studied in a batch adsorption system. The adsorption data were fitted well with the Langmuir isotherm models. The adsorption capacities (β) for Cd, Zn and Cu were 4.23, 2.93 and 3.64 mg/g in Type 1 and 1.24, 0.70 and 1.35 mg/g in Type 2 beads. The removal efficiencies of the Type 2 beads, with a larger unit surface area, were lower than those of the Type 1 due to part of the casein or cyclic AMP being destroyed during the drying process of the Type 1. These values for Type 1 beads were higher than those of all other adsorbents for each heavy metal. A comparison of the kinetic models on the overall adsorption rate showed that the adsorption system was best described by pseudo-first-order kinetics. The removal efficiencies of Cd, Zn and Cu exhibited similar tendencies to those observed in the equilibrium tests. This indicates that the jujube complex beads developed in this study can be used as promising adsorbents for the removal of heavy metals from wastewater.

The historical trend of heavy metal pollution recorded in sediment cores from Lake Shinji, western Japan, was investigated to evaluate the contribution of increasing long-range transport of heavy metals from the Asian continent in recent years. The concentrations of Cd, Co, Cr, Cu, Ni, Pb, Sb, and Zn and lead isotope ratios were determined for sediment cores collected at two sites in the lake. Among the metals, Cd, Sb, and Zn showed markedly high concentrations since the 1970s. Moreover, a high Pb concentration and less radiogenic lead isotope ratios have been observed since the 1980s in the core from a site close to the mouth of a major river. Air masses from the Asian continent, including China, Russia, and South Korea, have less radiogenic lead isotope ratios than those from Japan. This suggests that the recent increase in Pb concentration in the sediment core is primarily due to the long-range transport of heavy metals from the Asian continent, followed by their deposition in the catchment area of the river. The concentration ratios of Pb/Cd, Pb/Sb, and Pb/Zn of the sediment around 2000 were calculated on the basis of the metal concentrations in excess of those before 1940. They were then compared with the volume-weighted annual average concentration ratios of Pb/Cd, Pb/Sb, and Pb/Zn of rain samples collected on the shore of the lake for 1999–2001. The result showed that the ratios of the former to the latter are 1.0 for Cd, 0.69 for Sb, and 0.31 for Zn. Thus, it is likely that the long-range transport of Cd and Sb from the Asian continent also contributes significantly to the recent increase in the concentrations of these metals in the sediment core from Lake Shinji. For Zn, however, the contribution from the Asian continent was evaluated to be small, suggesting the importance of local sources such as effluent discharges.

The performance of a solar system designed to heat a packed bed reactor for anaerobic treatment of municipal wastewater was evaluated, and the feasibility of employing low-scale solar reactors in small settlements or enterprises was investigated. An energy balance was performed using a simple reactor model previously proposed by Yiannopoulos et al. (Bioresource Technology 99:7742–7749, 2008) to estimate the size of a solar system in Patras, Greece. The main objective is to feed the reactor with warm water produced by solar energy and achieve an increase of temperature close to 35°C for the majority of the year. Model simulations indicated that the heat demand of the reactor could be balanced practically by a number of flat plate solar collectors supplying warm water at above 20°C for over 95% of the year. Therefore, the proposed system can offer a viable alternative to enhancing anaerobic treatment in wastewater facilities.

The Loxahatchee National Wildlife Refuge (Refuge) is impacted by inflows containing elevated contaminant concentrations originating from agricultural and urban areas. Water quality was analyzed using the Enhanced Refuge (ERN), the four-part test (FPTN), and the Consent Decree (CDN) monitoring networks within four zones in the Refuge. The zones were defined as the canal surrounding the marsh, the perimeter, the transition, and the interior zones. Although regression coefficients for ALK and SpC, and Ca, Cl, and SO₄ concentrations with distance from the canal were lower using the FPTN than when using the ERN, using the FPTN to measure water quality parameters in the Refuge would give similar results as the ERN. Most of the ERN and FPTN sites are located in the northern and central areas of the Refuge. Water is deeper in the southern Refuge, and on an area basis contains a greater volume of water than the northern and central Refuge and therefore, water flow from the canal into the marsh in the northern and southern Refuge may differ. Numerous water quality monitoring sites must be added to the ERN and FPTN in the southern area to characterize water quality in the southern Refuge with confidence.

Cocamidopropyl hydroxysultaine (CAS) has been used in a pilot plant study as a biodegradable surfactant for the extraction of polycyclic aromatic hydrocarbons (PAHs) and lead (Pb) from contaminated soils. The soil treatment has been done in flotation cells with a concentration of 0.20 g CAS L−1 in saline conditions (3 M NaCl) and using a pulp density of 20% (w/w). The process integrates the recirculation of the liquid phases separated from the soil by centrifugation or filtration. Thus, it was necessary to understand CAS-PAHs micellar behavior and to follow the behavior and the fate of the surfactant in the process. 1-8-anilino-naphthalene sulfonate (ANS) is used as a fluorophor compound in the ANS enhanced fluorescence technique. A three-dimensional model detailing the change in the micellar behavior at high NaCl concentration and at different pH has been established. Fluorescence results of centrifuged soil matrix containing CAS have been compared to the results from synthetic solutions assays. A method allowing an accurate titration of the CAS has been developed by using the exact same matrix of the soil as the tested samples for the preparation of the calibration curves. The study of the surfactant concentration in the process has been performed and allows the adjustment of the CAS concentration in the recirculated water.