Oil refinery effluents contain many chemicals at variable concentrations. Therefore, it is difficult to predict potential effects on the environment. The Atibaia River (SP, Brazil), which serves as a source of water supply for many municipalities, receives the effluents of one of the biggest oil refinery of this country. The aim of this study was to identify the (eco)toxicity of fresh water sediments under the influence of this oil refinery through neutral red (cytotoxicity) and ethoxyresorufin-O-deethylase (EROD) assays (AhR-mediated toxicity) in RTL-W1 cells (derived from fish liver). Once the refinery captures the waters of Jaguarí River for the development of its activities and discharges its effluents after treatment into the Atibaia River, which then flows into Piracicaba River, sediments from both river systems were also investigated. The samples showed a high cytotoxic potential, even when compared to well-known pollution sites. However, the cytotoxicity of samples collected downstream the effluent was not higher than that of sediments collected upstream, which suggested that the refinery discharges are not the main source of pollution in those areas. No EROD activity could be recorded, which could be confirmed by chemical analyses of polycyclic aromatic hydrocarbons (PAHs) that revealed a high concentration of phenanthrene, anthracene, fluoranthene, and pyrene, which are not EROD inducers in RTL-W1 cells. In contrast, high concentrations of PAHs were found upstream the refinery effluent, corroborating cytotoxicity results from the neutral red assay. A decrease of PAHs was recorded from upstream to downstream the refinery effluent, probably due to dilution of compounds following water discharges. On the other hand, these discharges apparently contribute specifically to the amount of anthracene in the river, since an increase of anthracene concentrations could be recorded downstream the effluent. Since the extrapolation of results from acute toxicity to specific toxic effects with different modes of action is a complex task, complementary bioassays covering additional specific effects should be applied in future studies for better understanding of the overall ecotoxicity of those environments.
Papaya cultivation is widespread in Brazil, particularly in the states of Bahia and Espírito Santo, where most commercial plantations are concentrated. Owing to the economic and social importance of papaya, the present study aimed to determine the explanatory variables between the genotypes of two cultivars: Golden (from the Soil group) and Tainung Nº 1 hybrid (from the Formosa group), cultivated under high temperatures and hydric stress. The genotypes containing more desirable agronomic characteristics were identified for use in plant genetic improvement programs. Principal component analysis (PCA) was applied to select the desirable genotypes for Golden and Tainung Nº 1 cultivars based on specific variables analyzed for two groups of variables; for group 1, the plant height, stem diameter, leaf length, leaf width, and leaf number were analyzed, whereas for group 2, the leaf and root dry mass, stem dry mass and fresh mass of 10 discs, fresh mass, and stem and root fresh mass were analyzed. When exposed to hydric and thermal stress, the Tainung Nº 1 cultivar outperformed the Golden cultivar for the evaluation characteristics selected for use in genetic improvement programs.
The presence of salts in the culture medium and the addition of phytohormones, necessary to break seed dormancy in the in vitro germination of passion fruit, can induce critical values of osmotic potential. This can change the membrane permeability of seeds, affecting the hydration rate, enzyme release, ion transport, pH, and inhibitor values, which may decrease germination percentage. The aim of this study was to evaluate different types of culture media, composed of other substances, combined with mechanical techniques of tegument removal to determine the most appropriate culture medium for the in vitro germination of Passiflora edulis (Sims flavicarpa Deg.) seeds obtained by open pollination. The experimental design was completely randomized in a 10 × 3 factorial scheme (10 culture media × three types of seed-intact, scarified, and cut), with eight replicates and five seeds per plot. Scarified seeds cultivated in a medium composed of a commercial substrate and gibberellic acid presented a higher percentage of germination than intact or cut seeds cultivated in different concentrations of Murashige & Skoog (MS) medium. Scarification is a satisfactory method for breaking the dormancy of passion fruit seeds, and commercial substrates Bioflora® enriched with gibberellic acid may replace in vitro germination.
To evaluate the risks of hair dye exposure, we investigated cellular and molecular effects of Arianor Ebony dye, which is a mixture of azo and anthraquinone dyes, used in the composition of the black color. Cytotoxicity, genotoxicity, and gene expression of relevant molecules of apoptotic and oxidative stress mechanisms were investigated in HepG2 cells exposed to Arianor Ebony. Results showed that the dye did not induce cytotoxicity to exposed cells at a concentration up to 50 mg/mL compared to the negative control. However, genotoxic assays indicated that the dye was able to damage the genetic material at a concentration of 25 mg/mL, with induction factor values of exposed cells two-to five-fold higher than those recorded for the negative control. Moreover, the lowest observed effect concentration was 12.5 mg/mL. For gene expression, relevant changes were observed in cytochrome c and caspase 9, which decreased in cells incubated with the dye in a dose-dependent manner when compared with the negative control. In parallel, the expression of genes for antioxidant enzymes was increased in exposed cells, suggesting the presence of metabolic routes that protect cells against the toxic effect of the dye, avoiding exacerbated cellular death. Results suggested that the dye disrupted cellular homeostasis through mitochondrial dysfunction, which may be hazardous to human health. Thus, further investigations are necessary to deeply understand the mechanisms of action of the dye, considering its toxic potential found in our ex vivo assays.
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