Correlation between acute toxicity for Daphnia magna, Aliivibrio fischeri and physicochemical variables of the leachate produced in landfill simulator reactors.

Due to the diversified nature of municipal solid waste and the different stages of its decomposition, the formed leachates result in a complex chemical mixture with toxic potential. These chemicals can cause environmental problems, such as the contamination of surface or groundwater, thus affecting the balance of aquatic ecosystems. The aim of our study was to evaluate the acute toxicity of leachates in Daphnia magna and Aliivibrio fischeri and to identify the main physicochemical variables that influence the toxicity of the landfill leachates produced in reactors within pilot simulations. Acute toxicity tests carried out on D. magna and A. fischeri showed that the leachates produced inside the reactors are highly toxic, presenting EC5048h < 1% for D. magna and EC5015min < 12% for A. fischeri. This result indicates that microcrustaceans are more sensitive to leachates, making them more suitable to our study. Pb showed the highest correlation with EC5048h, suggesting that Pb is the main chemical variable indicative of toxicity for the conditions of the experiment. In smaller scale, phosphate (PO43-) and nitrate (NO3-) were the macronutrients that most influenced the toxicity. Clearly, this correlation should be viewed with caution because the synergistic effects of this complex mixture are difficult to observe.

Synthesis, characterization and toxicological evaluation of Cr2O3 nanoparticles using Daphnia magna and Aliivibrio fischeri.

Chromium III oxide (Cr2O3) nanoparticles (NPs) are used in pigments for ceramics, dyes, paints and cosmetics. However, few studies addressing the toxic potential of these NPs have been reported in the literature. Thus, this research aimed to evaluate the acute and chronic effects of Cr2O3 NPs through acute toxicity tests with Daphnia magna and Aliivibrio fischeri and chronic toxicity tests with Daphnia magna. Cr2O3 NPs were synthesized by the sol-gel method and characterized through TEM, X-Ray diffraction (XRD), zeta potential (ZP) and surface area analysis. In the acute toxicity tests the EC(50,48h) value obtained with D. magna was 6.79 mg L(-1) and for A. fischeri the EC(50,15min) value was 16.10 mg L(-1) and the EC(50,30min) value was 12.91 mg L(-1). Regarding the chronic toxicity tests with D. magna, effects on longevity (OEC=1.00 mg L(-1)), reproduction (OEC=1.00 mg L(-1)) and growth (OEC=0.50 mg L(-1)) were observed. On the SEM and TEM images, ultrastructural alterations in the organelles of exposed organisms were also observed. Thus, toxicological studies with NPs are of great importance in order to reduce the risk of environmental contamination.

Evaluation of Cytotoxicity and Cell Death Induced In Vitro by Saxitoxin in Mammalian Cells.

Since the cyanotoxin saxitoxin (STX) is a neurotoxin and induces ecological changes in aquatic environments, a potential risk to public and environmental health exists. However, data on STX-mediated cytotoxic and genotoxic effects are still scare. In order to gain a better understanding of the effects of this toxin, the cytotoxic and genotoxic potential of STX was examined in two mammalian cell lines. Neuro 2A (N2A), a neuroblastoma mouse cell line, and Vero cell line, derived from Vero green monkey kidney cells, were exposed to several concentrations of STX ranging from 0.5 to 64 nM to determine cell viability, induction of apoptosis (DNA fragmentation assay), and formation of micronuclei (MN) (cytokinesis-block micronucleus assay; CBMN) following 24 h of incubation. The half maximal effective concentration (EC50) values for STX calculated in cell viability tests were 1.01 nM for N2A and 0.82 nM for Vero cells. With increasing STX concentration there was evidence of DNA fragmentation indicating apoptosis induction in Vero cells with a 50% increase in DNA fragmentation compared to control at the highest STX concentration tested (3 nM). The results demonstrated no significant changes in the frequency of micronucleated binucleated cells in N2A and Vero cells exposed to STX, indicating the absence of genotoxicity under these test conditions. There was no apparent cellular necrosis as evidenced by a lack of formation of multinucleated cells. In conclusion, data reported herein demonstrate that STX produced death of both cell types tested through an apoptotic process.

Synthesis, characterization and toxicological evaluation of a core-shell copper oxide/polyaniline nanocomposite.

The newest generation of copper oxide NPs (CuO NPs) is the CuO core-shell (CS), which has potential applications in several areas (e.g., electronics and paint) and is able to provide a greater service life due to its coating; however, its toxicity is not fully understood. The objective of this study was to synthesize, characterize and evaluate the aquatic toxicology of CuO NPs and CuO core-shells through acute and chronic toxicity tests with the freshwater microcrustaceans Daphnia magna and to evaluate its acute toxicity with the marine bioluminescent bacteria Vibrio fischeri. The NPs were synthesized by direct thermal decomposition after being coated as a CS with polyaniline (PANI). With respect to acute toxicity with D. magna, the CuO NPs and CS CuO/PANI presented EC50 values of 0.32 mg L(-1) and 0.48 mg L(-1), respectively. For the tests with V. fischeri, the CuO NPs (EC50-15 min=7.79 mg L(-1)) exhibited behavior similar to that of the CS CuO/PANI (EC50-15 min=9.05 mg L(-1)) after 15 min of exposure. Regarding chronic toxicity, both forms showed a statistically significant effect (p<0.05) on the growth and reproduction parameters. Based on the characterization and toxicity results, it can be concluded that both forms of CuO were toxic and presented similar behaviors during the acute tests; however, after 21 d of exposure, CS CuO/PANI showed higher toxicity to the reproduction parameter, highlighting the importance of a complete study of the NP to better understand its toxicity mechanism.

Induction of micronucleus of Oreochromis niloticus exposed to waters from the Cubatão do Sul River, southern Brazil.

In an effort to characterize the pollution of surface waters by potentially genotoxic agents, this study aimed at assessing the frequency of micronucleated (MN) erythrocytes of the fish species, Oreochromis niloticus, from the Cubatão do Sul River. This river is the source of drinking water for the region of Florianópolis, capital of Santa Catarina State, Brazil. Negative control fish showed low frequency of MN, ranging between 0.49‰ and 0.90‰. Positive control (potassium dichromate 2.5 mg/L) organisms showed high MN frequency (16.82-17.25‰). The MN frequency increased along the river (Site 1--1.24‰ winter 2011; Site 4--9.76‰ summer 2011). Based on the observation of elevated MN erythrocytes frequency in O. niloticus exposed to water samples from along the river course, we conclude that the complex environmental mixtures of water from the Cubatão do Sul River have genotoxic potential. This genotoxicity most likely originated from agricultural runoff and domestic effluents released without treatment, based on the evidence from literature data and a survey in the region. This study provides a scientific basis for future studies regarding the genotoxicity of complex environmental mixtures in natural environments.

Preliminary assessment of the performance of oyster shells and chitin materials as adsorbents in the removal of saxitoxin in aqueous solutions.

BACKGROUND: This study evaluated the adsorption capacity of the natural materials chitin and oyster shell powder (OSP) in the removal of saxitoxin (STX) from water. Simplified reactors of adsorption were prepared containing 200 mg of adsorbents and known concentrations of STX in solutions with pH 5.0 or 7.0, and these solutions were incubated at 25°C with an orbital shaker at 200 RPM. The adsorption isotherms were evaluated within 48 hours, with the results indicating a decrease in STX concentrations in different solutions (2-16 µg/L). The kinetics of adsorption was evaluated at different contact times (0-4320 min) with a decrease in STX concentrations (initial concentration of 10 µg/L). The sampling fractions were filtered through a membrane (0.20 µm) and analyzed with high performance liquid chromatography to quantify the STX concentration remaining in solution. RESULTS: Chitin and OSP were found to be efficient adsorbents with a high capacity to remove STX from aqueous solutions within the concentration limits evaluated (> 50% over 18 h). The rate of STX removal for both adsorbents decreased with contact time, which was likely due to the saturation of the adsorbing sites and suggested that the adsorption occurred through ion exchange mechanisms. Our results also indicated that the adsorption equilibrium was influenced by pH and was not favored under acidic conditions. CONCLUSIONS: The results of this study demonstrate the possibility of using these two materials in the treatment of drinking water contaminated with STX. The characteristics of chitin and OSP were consistent with the classical adsorption models of linear and Freundlich isotherms. Kinetic and thermodynamic evaluations revealed that the adsorption process was spontaneous (ΔGads < 0) and favorable and followed pseudo-second-order kinetics.

Induction to oxidative stress by saxitoxin investigated through lipid peroxidation in Neuro 2A cells and Chlamydomonas reinhardtii alga.

Saxitoxin (STX) is a cyanotoxin, which can cause neurotoxic effects and induce ecological changes in aquatic environments, a potential risk to public and environmental health. Many studies of cytotoxicity on animal cells and algae have been performed, although few compare the toxic effects between the two models. In this sense, we investigated the oxidative stress induced by STX (0.4-3.0 nM) in two different cellular models: Neuro-2A (N2A) cells and Chlamydomonas reinhardtii alga by quantification of malondialdehyde (MDA) levels as indicative of lipid peroxidation (LPO). Also was evaluated the antioxidant defense of these cells systems after exposure to STX by the addition of antioxidants in N2A cells culture, and by the measure of antioxidants enzymes activity in C. reinhardtii cells. The MDA levels of N2A cells increased from 15% to 113% for 0.4 and 3.0 nM of STX, respectively, as compared to control. Superoxide-dismutase and catalase did not appear to protect the cell from STX effect while, in cells treated with vitamin E, the rates of MDA production decreased significantly, except for higher concentrations of STX. No MDA productions were observed in algal cells however some effects on antioxidant enzymes activity were observed when algae were exposed to 3.0 nM STX. Our results indicate that the concentrations of STX that may induce oxidative stress through LPO are different in animal and phytoplankton communities. A combination of algal and animal bioassays should be conducted for reliable assessment of oxidative stress induced by STX.