The present study investigated the impact of solar UV radiation on ZnO nanoparticle toxicity through photocatalytic ROS generation and photo-induced dissolution. Toxicity of ZnO nanoparticles to Daphnia magna was examined under laboratory light versus simulated solar UV radiation (SSR). Photocatalytic ROS generation and particle dissolution were measured on a time-course basis. Two toxicity mitigation assays using CaCl2 and N-acetylcysteine were performed to differentiate the relative importance of these two modes of action. Enhanced ZnO nanoparticle toxicity under SSR was in parallel with photocatalytic ROS generation and enhanced particle dissolution. Toxicity mitigation by CaCl2 to a less extent under SSR than under lab light demonstrates the role of ROS generation in ZnO toxicity. Toxicity mitigation by N-acetylcysteine under both irradiation conditions confirms the role of particle dissolution and ROS generation. These findings demonstrate the importance of considering environmental solar UV radiation when assessing ZnO nanoparticle toxicity and risk in aquatic systems.

Microcystin-LR (MC-LR), one of the most common cyanotoxins, is produced by harmful cyanobacteria. The current study focuses on the photosensitized transformation of MC-LR in dissolved organic matter (DOM) enriched solutions under solar simulated irradiation. It appears that the direct energy transfer of triplet excited state DOM with MC-LR plays a key role and leads to photosensitized isomerization of Adda side chain. Furthermore a micro-heterogeneous mechanism has been proposed. Size exclude chromatograph (SEC) has been applied to explore the adsorption of MC-LR on the DOM. The adsorption phenomenon supported the fact that the pseudo first-order photodegradation rates showed positive correlation with the adsorption. The photo-transformation rate of MC-LR increases as pH decreases which is also the result of the adsorptive interaction of MC-LR with DOM. Finally two bulk water parameters (TOC and UV350 nm) have been applied to predict the photodegradation rates of MC-LR in the varied water matrixes.

Review is devoted to the analysis of a radioecological situation in the North-western Black Sea and concerns the levels of contamination of the components of an ecosystem by the main artificial radioactive isotopes (90Sr, 137Cs, 239,240Pu). The long-term accumulation trends of these radionuclides were analyzed in components of the Black Sea ecosystem after the Chernobyl nuclear power plant accident. Zones that have an increased ability to accumulate these radioisotopes were revealed. The assessment of irradiation dose rates formed by 90Sr, 137Cs and 239,240Pu in Black Sea hydrobionts was obtained. The strategy for biodiversity conservation and sustainable management of natural resources should include monitoring of the radioecological state of the marine ecosystems, and the formation of a complex of biogeochemical criteria for assessment of an ecological situation in the sea. This approach is important for marine protected areas, since it allows the formation of a basis for scientific and practical function.

The northern Gulf of Aqaba is an oligotrophic water body hosting valuable coral reefs. In the Gulf, phytoplankton dynamics are driven by an annual cycle of stratification and mixing. Superimposed on that fairly regular pattern was the establishment of a shallow-water fish-farm initiative that increased gradually until its activity was terminated in June 2008. Nutrient, water temperature, irradiation, phytoplankton data gathered in the area during the years 2007–2009, covering the peak of the fish-farm activity and its cessation, were analyzed by means of statistical analyses and ecological models of phytoplankton dynamics. Two datasets, one from an open water station and one next to the fish farms, were used. Results show that nutrient concentrations and, consequently, phytoplankton abundance and seasonal succession were radically altered by the pollution originating from the fish-farm in the sampling station closer to it, and also that the fish-farm might even have influenced the open water station.

Novel photocatalysts i.e., metallic nickel and zinc oxide nanoparticles embedded in the carbon-shell ((Ni–ZnO)@C) have been used for photocatalytic splitting of seawater to generate H2. The (Ni–ZnO)@C core–shell nanoparticles having the Zn/Ni ratios of 0–3 were prepared by carbonization of Ni2+- and Zn2+-β-cyclodextrin at 673K for 2h. To increase the collision frequency of water and photoactive sites within the carbon-shell, Ni and ZnO are partially etched from the (Ni–ZnO)@C core–shell to form yolk–shell nanoparticles with a H2SO4 solution (2N). By X-ray diffraction spectroscopy, mainly Ni and ZnO crystallites are observed in the core– and yolk–shell nanoparticles. The sizes of the Ni and ZnO in the (Ni–ZnO)@C nanoreactors are between 7 and 23nm in diameters determined by TEM and small angel scattering spectroscopy. Under a 5-h UV–Vis light irradiation, 5.01μmol/hgcat of H2 are yielded from photocatalytic splitting of seawater effected by (Ni–ZnO)@C nanoreactors.

The effects of several aquatic environmental factors on the photochemical transformation of 2,2′,4,4′-tetrabromodiphenyl ether (BDE-47) have been investigated. Ferric ion (Fe(III)) has been found to promote the phototransformation of BDE-47, and this process is further enhanced with the added chloride ion (Cl−), while it is suppressed with increasing pH. Electron spin resonance results show that the formation of hydroxyl radical, and the added Cl− could influence the generation of hydroxyl radical in Fe(III) solution. Hence, Cl− enhances the phototransformation of BDE-47 most probably because of the reaction with Fe(III) species under irradiation, yielding hydroxyl and chloride radicals. These radicals can not only decompose PBDEs, but also lead to their photodebromination and photochlorination. These results indicate that the aquatic environmental factors and Cl− in particular played an important role in the photochemical transformation process of PBDEs, providing insight into the likely fate of PBDEs in the marine environment.

The present study was conducted on clover (Trifolium alexandrinum L. cv Wardan), to investigate the effect of ambient and elevated (ambient +10 ppb O3) ozone (O3) on plants grown in open top chambers (OTCs) germinated from gamma (γ) irradiated seeds. Dry seeds were subjected to irradiation with 0, 5, 10 and 20 krad doses of γ rays from 60Co source. Dose dependent differential responses were observed on growth and biomass, photosynthetic pigments, metabolites, antioxidative defense system of plant. Growth parameters and biomass of plants were severely affected under elevated O3 with increasing radiation doses, except, 5 krad which showed a reverse trend of response. Photosynthetic pigments and total soluble proteins were also reduced with higher dose of γ radiation and elevated O3. Reactive oxygen species formation and membrane damage increased significantly to different extents. Plants grown from seeds irradiated with low dose (5 krad) of γ irradiation depicted more induction of antioxidants (enzymatic and non–enzymatic) than higher doses suggesting their high ameliorative capability against elevated O3. Principal component analysis has also confirmed that plants grown from 5 krad γ irradiated seeds performed better against O3 depicting reduction in negative effect against elevated O3. The experimental findings evidently showed that 5 krad γ radiations altered the O3 induced stress and thus minimized the loss in biomass of the test plant.

The coffee agro-industry generates a large volume of wastewater that is notable for its high organic strength as well as its color content. Due to the seasonal nature of the harvest (3–4 months per year), this particular industrial waste needs a treatment method that is both reliable and fast (in terms of start-up time). As part of investigating a system capable of treating a coffee wastewater, this research evaluated four electrochemical advanced oxidation processes (EAOPs) using boron-doped diamond (BDD) electrodes. The processes were anodic oxidation (AO), anodic oxidation with electrogenerated H₂O₂(AO-H₂O₂), electro-Fenton (EF), and photoelectro-Fenton (PEF). Experimental conditions were as follows: 40 mA cm⁻²current density (all EAOPs), 0.3 mmol Fe²⁺L⁻¹(Fenton systems), 300 mL air min⁻¹(AO-H₂O₂, EF, PEF), and 500 μW cm⁻²UV irradiation (photo-Fenton systems). The performance of the four EAOP treatment methods (in terms of color and organic carbon removal) was compared against two conventional chemical oxidation methods, namely, Fenton and photo-Fenton. The research indicated that the four EAOPs were better at removing color (89–93 %) and total organic carbon (TOC) (73–84 %) than the respective chemical Fenton (58 and 4.8 %) and photo-Fenton (61 and 7 %) methods. The trend in performance was as follows: AO-H₂O₂ > AO > PEF ≈ EF. It appeared that the ferrous iron reagent formed a dark-colored complex with some coffee components, diminishing the effect of Fenton reactions. In addition, the dark color of the wastewater limited the effect of light in the UV-Fenton processes. Analysis showed that acceptable levels of Fe²⁺(0.3 mmol L⁻¹) and energy (0.082–0.098 kWh g⁻¹TOC) were required by the EAOPs after 4-h treatment time. In conclusion, the use of electrochemical methods (equipped with BDD electrodes) seems a promising method for the effective treatment of coffee wastewaters.

The transformation of less toxic Cr(III) species to harmful Cr(VI) is worth concerning. Compared with free Cr(III), however, the photo-oxidation of Cr(III)–organic acid complexes is seldom reported. In this study, Cr(III)–malate complex was synthesized and purified, and its photo-oxidation was investigated to reveal the potential conversion pathway of Cr(III) to Cr(VI). The results indicated that Cr(III)–malate complex could be gradually photo-oxidized to Cr(VI) through a ligand–metal charge transfer path. Higher pH and stronger light intensity promoted the conversion process. A 50-μM Cr(III)–malate complex was almost completely oxidized to Cr(VI) within 420-min irradiation of 500 W medium-pressure mercury lamp at pH 12. The introduction of H₂O₂, considered as a direct source of hydroxyl radicals (·OH) in the presence of Cr(II), markedly enhanced the yield of Cr(VI), and a complete oxidation of Cr(III)–malate complex (50 μM ) was realized within 20 min. Under a weak acidic condition, the production of Cr(VI) was coupled with the reduction of Cr(VI) by malic acid and its free radical generated from Cr(III)–malate complex, leading a gradual decrease in Cr(VI) concentration with the reaction.

The degradation of methyl orange (MO) in aqueous solution by microwave irradiation in the presence of granular-active carbon (GAC) was investigated. It was found that a synergistic rather than an additive effect of microwave irradiation and GAC contributes to the high-degradation efficiency. The ultraviolet and visible spectrum (UV–vis), infrared spectroscopy (IR), and scanning electron microscopy (SEM) measurements were conducted to trace the MO degradation process. It was demonstrated that the decrease in performance of GAC after repetitive use is largely attributed to the adsorption of some intermediate products on the surface of GAC. The regeneration of the spent GAC under microwave radiation was also investigated. The results show that the activity of spent GAC can be effectively recovered by microwave radiation and 74.1 % of its initial activity remains after six reaction cycles.