In this study, microalgae Scenedesmus quadricauda was entrapped in calcium alginate/polyvinyl alcohol composite hydrogel beads by phase-inversion techniques. The composite biosorbents were used for removal of Cu(II) and Cd(II) ions from single component and binary systems using cell-free composite beads as a control system. The effects of the experimental conditions (such as pH, initial metal ions concentrations, temperatures, contact time, and biosorbent concentrations) on Cu(II) and Cd(II) removal efficiencies were studied. The maximum metal ions on the bare and algal biomass immobilized in alginate beads were observed between pH 5.0 and 6.0. The biosorption of metal ions by the bare and composite beads increased as the initial concentration of the metal ions increased in the medium. The biosorption of Cu(II) and Cd(II) on the composite beads appears to be slightly temperature dependent. The maximum biosorptions of metal ions onto microalgae entrapped in composite beads were 0.970 ± 0.028 and 0.682 ± 0.017 mmol/g for Cu(II) and Cd(II) ions, respectively. The equilibrium experimental data for two metallic species fitted well by the Langmuir model. The values of ΔG° at all temperatures are negative, indicating the spontaneous nature of the biosorption process. When the metal ions competed (in the case of the biosorption from their mixture), the amounts of biosorption onto microalgae cells entrapped in beads were 0.857 ± 0.033 mmol/g for Cu(II) and 0.593 ± 0.024 mmol/g for Cd(II). Under noncompetitive and competitive conditions, the affinity order of ions for biosorbents was Cu(II) > Cd(II).

The polluted site object of our study was located on an island nourished using different materials, including industrial by-products, inside the area of Porto Marghera (Venice Lagoon, Italy). Until the 1970s, this area was one of the most important chemical districts in Italy and was largely subjected to heavy metals and metalloids pollution. In the year 2004, some Populus and Salix spp. had been planted in this polluted site in order to investigate both the hydrological control and the phytoremediation capability of these trees. In the present work, polluted soil was analyzed at different depths for both metals content and culturable microbial communities with the aim to evaluate the establishment of previously planted poplar and willow plants. Bacteria were characterized on the basis of the r/K-strategists distribution since r-strategists (fast-growing bacteria) and K-strategists (slow-growing bacteria) are characteristic for unstable and stable environments, respectively. A better characterization of bacterial communities composition was obtained from colony development and eco-physiological indices. Results appeared to confirm a good establishment of poplar and willow plants in the heavy metal contaminated site.

Recently, there has been increasing concern about perfluorinated compounds, especially perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA) due to their biotic and abiotic persistence and chronic toxicity. To characterize the spatial distribution and seasonal variation of PFOS and PFOA in the aquatic and oceanic environment of Singapore, more than 100 water samples from reservoirs, rivers/canals, coastal waters, and treated effluents of wastewater treatment plants (WWTPs) were collected and analyzed in this study. Solid-phase extraction followed by high-performance liquid chromatography (HPLC) coupled with tandem MS (HPLC/MS/MS) was applied to quantitatively identify PFOS and PFOA. PFOS concentrations in surface waters, wastewaters and coastal waters were in the range of 2.2–87.3 ng/L, 5.8–532 ng/L, and 1.9–8.9 ng/L, respectively, while those of PFOA were 5.7–91.5 ng/L, 7.9–1,060 ng/L, 2.4–17.8 ng/L, respectively. Compared with surface waters and wastewaters, coastal waters had lower concentrations of PFOS and PFOA. Highest concentration of PFOA (532 ng/L) and PFOA (1,060 ng/L) were observed in treated effluents of two WWTPs. Our results suggest that coastal waters in the western area of Singapore are more heavily contaminated than those in the middle and eastern areas. The release of effluents from WWTPs is an important pathway by which perfluorinated compounds enter the oceanic environment. Between dry season and wet season, significant seasonal differences (p = 0.025) were observed in surface waters for PFOS only, while no discernable seasonal differences were found for both PFOS and PFOA in coastal waters and wastewaters.

Pharmacologically active substances used in the treatment of human and animal illnesses may usually enter the aquatic environment via effluents from sewage treatment plants, as they are not completely biodegraded or removed during waste water treatment. 17β-Estradiol genotoxicity was evaluated in Oreochromis niloticus (family Cichlidae) using micronucleus test, other nuclear abnormalities assessment, and the comet assay with erythrocytes. Fish were exposed to aqueous systems contaminated with 6 ng/L 17β-estradiol for three periods: 24 h, 48 h, and 10 days. The results showed that 17β-estradiol has genotoxic potential in different periods, since significant differences (P = 0.036) were observed in the micronucleus frequencies of the 10-day exposure groups in relation to the control group. Also, the same was observed when comparing the nuclear abnormality frequencies (P = 0.018) of the 24-h exposure group with the negative control group, and when using comet assay (P < 0.001) for 48-h evaluations. The tested concentration of the 17β-estradiol gave rise to mutagenic and genotoxic effects on the blood cells of O. niloticus, therefore the substance being considered a clastogenic chemical contaminant on both acute and chronic exposures. The assessment using a combination of micronucleus test, nuclear abnormalities, and comet assays proved to be suitable and useful in the genotoxicity testing of 17β-estradiol at nanograms per liter.

A 9-month-long continuous flow column study was carried out to investigate Cr(VI) removal by Fe0 with the presence of humic acid. The study focused on the influences of humic acid promoted dissolved iron release and humic acid aggregation in Fe0 columns receiving synthetic Cr(VI) contaminated groundwater containing various components such as bicarbonate and Ca. The effects of humic acid varied significantly depending on the presence of Ca. In Ca-free columns, the presence of humic acid promoted the release of dissolved iron in the forms of soluble Fe-humic acid complexes and stabilized fine Fe (hydr)oxide colloids. As a result, the precipitation of iron corrosion products was suppressed and the accumulation of secondary minerals on Fe0 surfaces was diminished, and a slight increase in Cr(VI) removal capacity by 18% was record compared with that of humic acid-free column. In contrast, in the presence of Ca, as evidenced by the SEM and FTIR results, humic acid greatly co-aggregated with Fe (hydr)oxides and deposited on Fe0 surfaces. This largely inhibited electron transfer from Fe0 surfaces to Cr(VI) and reduced the drainable porosity of the Fe0 matrix, resulting in a significant decrease in Cr(VI) removal capacity of Fe0. The Cr(VI) removal capacity was decreased by 24.4% and 42.7% in humic acid and Ca receiving columns, with and without bicarbonate respectively, compared with that of Ca and humic acid-free column. This study yields new considerations for the performance prediction and design of Fe0 PRBs in the environments rich in natural organic matter (NOM).

Different substrates were evaluated to investigate their effect on nitrate removal and denitrifying bacterial community in soils obtained from wetland. Serial batch kinetic tests were conducted on soils obtained from wetland mixed with glucose and sawdust using KNO3 solution. Column tests were also conducted on soils obtained from wetland mixed with three different substrates (glucose, sawdust, and scoria coated with zero-valent iron) using KNO3 solution. For the batch tests, the nitrate removal efficiency for soil mixed with glucose was comparable to that for soil mixed with sawdust, but the nitrate removal rate for soil mixed with glucose (23.3 NO3 −-N mg/L-d) was approximately eight times higher than that for soil mixed with sawdust (2.8 NO3 −-N mg/L-d). For column tests among soil samples, nitrate removal efficiency was highest in soil mixed with glucose, which is an easily biodegradable carbon source. Removal efficiency increased with increasing incubation time for both soil samples with glucose and sawdust. A phylogenetic analysis based on nitrate reductase gene demonstrated that the different carbon sources affected both the diversity and compositions of the denitrifying bacterial in soil samples.

The sequential elution technique (SET) is used to determine the distribution of elements in the different cell fractions of mosses. The extracellular extractants most commonly used in this technique are NiCl2 and EDTA, although there are certain disadvantages associated with their use. In order to avoid such problems, we searched for new extractants that displace extracellularly bound metals, either because they are present at high concentrations (Ca) or because they have a high affinity for cation exchange sites (Hg and Au). The compounds HCl, NaCl, and CaCl2 were tested as extractants of the former type, as possible alternatives for the determination of extracellular metals in the moss Pseudoscleropodium purum. Calcium chloride was finally chosen as is it potentially the most successful in terms of binding to the cation exchange sites without altering the membrane permeability. The concentration chosen was 160 mM, as this yielded maximum displacement of Zn without membrane alterations. An experiment was then carried out to test the efficiency of Ca in extracting extracellular Zn, under laboratory and field conditions. In addition, Hg and Au were tested, at different concentrations, as extractants with high affinity for cation exchange sites, as neither of these elements has previously been used in the SET, and both display electronic characteristics that suggest their potential usefulness in displacing other cations from cation exchange sites. The results obtained show that extraction of extracellularly bound metal by high concentrations of Ca should be ruled out, as total extraction of Zn was not achieved. Both Hg and Au produced membrane alterations at low concentrations and moreover, neither was more efficient at extracting Zn than the reference extractant (20 mM NiCl2).

There are several classes of subsurface colloids, abiotic and biotic. Basically, small particles of inorganic, organic and pathogenic biocolloids variety exist in natural subsurface system. Transport of these pathogenic biocolloidal contaminants (Viruses, bacteria and protozoa) pose a great risk in water resources and have caused large outbreaks of waterborne diseases. Biocolloid transport processes through saturated and unsaturated porous media is of significant interest, from the perspective of protection of groundwater supplies from contamination, assessment of risk from pathogens in groundwater and for the design of better water treatment systems to remove biocolloids from drinking water supplies This paper has reviewed the large volume of work that has already been done and the progress that has been made towards understanding the various basic multi-processes to predicting the biocolloid transport in saturated and unsaturated porous media. There are several basic processes such as physical, chemical and biological processes which are important in biocolloid transport. The physical processes such as advection, dispersion, diffusion, straining and physical filtration, adsorption and biological processes such as growth/decay processes and include active adhesion/detachment, survival and chemotaxis are strongly affected on biocolloid transport in saturated and unsaturated porous media. The unsaturated zone may play an important role in protecting aquifers from biocolloidal contamination by retaining them in the solid phase during their transport through the zone. Finally, author here highlighted the future research direction based on his critical review on biocolloid transport in saturated and unsaturated porous media.

Photocatalytic degradation of bisphenol A (2,2-bis(4-hydroxyphenyl)propane, BPA), a representative endocrine-disrupting compound, was carried out in the presence of the Ti-MCM-41 mesoporous molecular sieve in this investigation. The degradation rate was strongly dependent on those factors such as the catalyst, catalyst amount, radiation time, and pH value. The photolysis reaction was found to follow the Langmuir-Hinshelwood model. After the photocatalytic treatment, decomposition of BPA rendered five intermediates as follows: 2-methyl-2,3-dihydrobenzofuran, 4-hydroxyacetophenone, 1,1-diethoxyethane, isobutanol, and 3-methylbutanal, which could be the direct evidence supporting our proposal for the degradation mechanism.

The main goals of this study were (1) to standardize a simple and reliable embryotoxicity test for environmental contaminants and (2) to evaluate the presence and possible protective role of the multidrug resistance-associated (MRP) protein-mediated multixenobiotic defense in two Mediterranean sea urchin species, Paracentrotus lividus and Arbacia lixula. Toxic end-point used was the success of the first cell division in sea urchin embryos. Embryotoxicities of three environmentally relevant contaminants: mercuric chloride (HgCl2, 0.05–6 μM), trybutiltin (TBT, 2.5–500 nM), and oxybenzone (OXI, 0.1–100 μM); as well as seawater samples collected from the polluted and unpolluted locations, were determined and compared. A. lixula embryos were more sensitive to all three toxic compounds, and both P. lividus and A. lixula embryos were highly sensitive to TBT at nanomolar concentrations (EC50 49 ± 5 and 36.8 ± 3 nM, respectively). Inhibition of MRP protein by specific inhibitor MK571 caused significant increase in embryotoxic potency of HgCl2 (EC50 0.697 ± 0.03 and 0.245 ± 0.04 μM, respectively), TBT (EC50 24 ± 3 and 7.4 ± 1 nM, respectively) and polluted seawater sample, but not of OXI or unpolluted, natural seawater. Therefore, our results demonstrated for the first time the protective relevance of MRP proteins in early development of these two Mediterranean sea urchin species. Finally, the embryotoxicity protocol described in this study represents a simple and rapid bioassay for determination of environmentally relevant seawater contamination.