Relationships between total suspended solids (TSS) and metals (Cu, Pb and Zn) were tested and compared amongst base and high flows of three urbanised catchments in Sydney Estuary, Australia. Significant relationships between TSS and Cu, Pb and Zn were detected for high flows within each catchment; however, no significant relationship was detected for TSS/Zn and TSS/Cu in one of the creeks (Whites Creek) and for TSS/Zn in another (Hawthorne Canal) in 2010 during base flow. Relationships between metals and TSS also varied significantly in locations of intercept and slope between high and base flow and amongst catchments. Spatial variance in TSS/metal relationships were likely caused by specific anthropogenic activities because land uses, meteorology and geology within the study catchments were similar. Results suggest TSS may be used as a surrogate for estimating metal loading in real time for urban catchments, once relationships between metals and TSS were established for individual catchments and for base and high flow conditions. Moreover, no differences in TSS/metal relationships were detected between 2009 and 2010 in Hawthorne Canal during high flow conditions, suggesting that this method of real-time monitoring may be reliable for assessing Cu, Pb and Zn loads during high flows over inter-annual periods. However, long-term consistency of TSS/metal relationships for base flow may need testing since changes in TSS/Zn and TSS/Cu relationships were detected between 2009 and 2010 in Hawthorne Canal. Although irregular discharges to stormwater did not conform to TSS/metal relationships, irregular discharges may be detected in real time by increased flow during dry weather conditions, which may facilitate regulation of these conditions that currently result in potential environmental harm to aquatic biota in Sydney Estuary.

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.

Mangrove ecosystems are tropical environments that are characterized by the interaction between the land and the sea. As such, this ecosystem is vulnerable to oil spills. Here, we show a culture-independent survey of fungal communities that are found in the sediments of the following two mangroves that are located on the coast of Sao Paulo State (Brazil): (1) an oil-spill-affected mangrove and (2) a nearby unaffected mangrove. Samples were collected from each mangrove forest at three distinct locations (transect from sea to land), and the samples were analyzed by quantitative PCR and internal transcribed spacer (ITS)-based PCR-DGGE analysis. The abundance of fungi was found to be higher in the oil-affected mangrove. Visual observation and correspondence analysis (CA) of the ITS-based PCR-DGGE profiles revealed differences in the fungal communities between the sampled areas. Remarkably, the oil-spilled area was quite distinct from the unaffected sampling areas. On the basis of the ITS sequences, fungi that are associated with the Basidiomycota and Ascomycota taxa were most common and belonged primarily to the genera Epicoccum, Nigrospora, and Cladosporium. Moreover, the Nigrospora fungal species were shown to be sensitive to oil, whereas a group that was described as “uncultured Basidiomycota” was found more frequently in oil-contaminated areas. Our results showed an increase in fungal abundance in the oil-polluted mangrove regions, and these data indicated potential fungal candidates for remediation of the oil-affected mangroves.

In this experiment, the effects of the Hungarian red mud disaster were studied in a soil column experiment focusing on element solubility. The effect of flooding with the highly alkaline red mud suspension and the effect of the percolation of precipitation water through the 10 cm thick red mud layer were modelled separately. Both scenarios affected the soil pH up to a depth of 80 cm. An increase in the total element concentration was only observed for Na and Mo, probably due to the leaching of red mud particles measuring 0.05–0.02 and <0.002 mm in the column. At the same time, the water-soluble concentrations of the potentially toxic elements As, Co, Cr, Cu, Ni, Pb, and Zn rose, at least in the top soil layer, but the concentration values remained below the limit values laid down by quality standards. Over a longer period of time, the main environmental risk raised by the disaster is the secondary salinization of the area.

To evaluate plant responses and compare metal uptake by different plants, several parameters and references have been used by researchers in the last few years. However, they express only the first-level comparison, i.e. biogeochemical comparison of different media (plant and soil) occurs in one place, at the same time and under the same circumstances. To integrate information about metal concentration in different media or plant organ and provide comparison of the process between control and treated cases, the second-level factors, the dynamic factors, are needed. Differently from the factors mentioned in the existing literature, they are able to show changes in processes under environmental changes rather than changes only in metal quantities. They are related both to internal (physiological) and external (ecological) factors. The paper introduces the use of dynamic factors for assessment of transfer and translocation of metals (Zn, Pb, Ni, Mn, Cu and Cr) in Scots pine (Pinus sylvestris L.), silver birch (Betula pendula) and black alder (Alnus glutinosa). Factor values and their implications are discussed in the paper.

This work assesses the use of immobilized humic acid (ImHA) onto aminopropyl silica (APS) as a sorbent for the removal and preconcentration of trace amounts of cobalt ions by on-line solid phase extraction (SPE) technique in the column system prepared in our laboratory. Different parameters, such as the effect of the pH, concentration, and flow rate, were studied and throughput was observed by a UV detector. All SPE steps were monitored by breakthrough curves used to visualize distribution of cobalt concentration between mobile and solid phase. The solutions collected from stripping steps were analyzed in atomic absorption spectrometer (AAS) and the amount of sorbed ions was calculated. Sorption characteristics were evaluated by using common adsorption isotherms and Scatchard plot analysis. From the obtained results, it was seen that sorption mechanism of cobalt ions were fitted to Langmuir model on a large scale and thought to be localized. Mean free energy (E = 40.82 kJ mol⁻¹) calculated from D-R isotherm showed that chemical interactions are more effective than physical interactions. This investigation reveals a new, simple, environmentally friendly, and cost-effective method for removal and preconcentration of cobalt ions from aqueous solutions by a new aminopropyl silica-immobilized humic acid material.

Three different solventless sample preparation techniques based on microextraction, membrane extraction, and headspace extraction have been developed and optimized for determination of trihalomethanes in drinking water by gas chromatography electron capture detector and mass spectrometry detection. The techniques employed were headspace (HS) solid-phase microextraction, hollow fiber liquid-phase microextraction (HFLPME) and HS extraction. All techniques used were optimized with different experimental designs in order to select the most relevant variables which significantly affect the different processes. The different analytical figures of merit such as limit of detection (LOD), limit of quantification, reproducibility, accuracy, and linear dynamic range were obtained. The new HFLPME method applied used a hollow fiber membrane of polypropylene and the optimized variables were extraction time, extraction temperature, and salting-out effect. The software MODDE 6.0 was used and its design was one central composite on face with a total of 17 runs. The best conditions for the HFLPME were 20 min, 40°C, and 10% NaCl, respectively. The LODs ranged from 0.018 μg·L−1 (for CHClBr2) to 0.049 μg·L−1 (for CHBr3), being this technique the most sensitive one among those studied. Finally, after having optimized the sample preparation techniques and chromatographic conditions, several water samples were taken in two different water treatment plants in Spain (Zaragoza) and Colombia (Viterbo, Caldas). The results obtained are shown and discussed.

Since usual processes involve water as absorbent, they appear not always really efficient for the treatment of hydrophobic volatile organic compound (VOC). Recently, absorption and biodegradation coupling in a two-phase partitioning bioreactor (TPPB) proved to be a promising technology for hydrophobic compound treatment. The choice of the organic phase, the non-aqueous phase liquid (NAPL) is based on various parameters involved in both steps of the process, hydrophobic VOC absorption in a gas–liquid contactor, and biodegradation in the TPPB. VOC solubility and diffusivity in the selected NAPL, as well as NAPL viscosity, seems to be the main parameters during the absorption step, while biocompatibility, namely the absence of toxic effect of the NAPL towards microorganisms, non-biodegradability and VOC partition coefficient between NAPL and water were revealed as the key factors during the biodegradation step. The screening of the various NAPL available in the literature highlighted two families of compounds matching the required conditions for the proposed integrated process, silicone oils and ionic liquids.

Atmospheric pollution is known to induce corrosion effects on various materials. For Greece, stone deterioration could emerge severe costs in the case of damaging cultural monuments. This work aims to investigate the corrosion process on materials of archaeological importance (marble, limestone, and sandstone) in the Greater Athens Area (GAA) by using sophisticated geoanalytical methods together with dose–response functions for selected materials, in order to derive corrosion maps for GAA in the period 2000–2009. Also, a corrosion trend analysis is performed, which can be a very helpful tool for the prediction of potential risks to monuments of cultural heritage due to atmospheric pollution. The corrosion effects on the selected materials are generally weak. Nevertheless, increasing corrosion trends are found in the eastern regions of GAA for all sheltered materials and in the northern parts of GAA for unsheltered marble. The technique is finally applied to 12 locations in GAA, which include some of the most important archaeological monuments of Athens, and provides comprehensive results for the estimation of the impact of atmospheric corrosion on the structural materials of these archaeological sites.