Utilization of metal and radionuclide concentrations to assess the influence of shrimp farming on the geochemical characteristics of sediments.

This article assesses the environmental impacts of aquatic biota cultivation, focusing on shrimp farming in Brazil's Northeast, as this practice has proven to be one of the main sources of economic growth in the region. For this purpose, sediment samples were collected from areas impacted and not directly impacted by shrimp farming, and concentrations of key geochemical parameters such as salinity, various elements (K, P, Cu, Mn, Pb, Zn, Al, Ca, Fe, Mg, and Na), and natural radionuclides (K-40, Ra-226 and Ra-228) were compared using statistical tools. Element concentrations were determined using ICP-OES, and naturally occurring radionuclide concentrations were obtained through gamma spectrometry. Statistical tests, such as ANOVA and/or Mann-Whitney, cluster analysis, and principal component analysis, were applied to the results. Additionally, the ERICA Tool software was employed to estimate deleterious effects on both human and non-human biota. Descriptive statistics reveal variability in sediment parameters around shrimp farming. ANOVA and Mann-Whitney tests compare concentrations of shrimp farm sediment and not directly impacted sediment, showing non-significant differences for most elements. pH and salinity, crucial for shrimp health, exhibit higher values in shrimp farm sediment. Alkali and alkaline earth metals, including K and Na, show no significant differences. Factor and cluster analyses suggest that certain elements, mainly radionuclides, are influenced by sediment variability. Hazard indices for naturally occurring radionuclides indicate negligible risk to both human and non-human biota, reinforcing the absence of adverse effects from shrimp farming activities. This study provides a comprehensive analysis of the environmental impacts of shrimp farming, emphasizing the importance of monitoring geochemical parameters for coastal environmental management.

A photobioreactor using Nannochloropsis oculata marine microalgae for removal of polycyclic aromatic hydrocarbons and sorption of metals in produced water.

The objective of the present work is to evaluate the potential of the removal of PAHs and metal sorption for the treatment of petroleum produced water using a photobioreactor system with Nannochloropsis oculata microalgae. A set of photobioreactors with different gradients of produced water concentration diluted in saline water was designed, establishing five gradients (v/v): 0, 25, 50, 75 and 100%. These concentrations were established to test the removal of PAHs. The microalgal growth was monitored daily, noting the adaptation of microalgae to the addition of produced water as a culture medium, with cell growth of 5.24 × 107 cells mL-1 from 25% (v/v), 4.09 × 107 cells mL-1 from 50% (v/v), 2.77 × 107 cells mL-1 from 75% (v/v), and 1.17 × 107 cells mL-1 from 100%. The total removal efficiency of PAHs in the produced water was 94%. Organic compounds such as naphthalene, benzo(a)pyrene, benzo(b)fluoranthene, and acenaphthylene showed higher removal percentages, between 89 and 99% efficiency in produced water. Iron and zinc were the metals detected in the water produced, and iron reduced from 1.57 ± 0.08 mg L-1 to <0.1 mg L-1 after 28 days of cultivation, whereas zinc increased by 0.23 ± 0.05 to 3.90 ± 0.46 mg L-1. The PAHs removal may have occurred in two ways, by intracellular bioaccumulation or biodegradation by oxidoreductase enzymes. 0.2 g of dry biomass with maximum extraction of oil obtained 3.07% and generation of 3.70% of protein was considered as value-added products for biodiesel and bioplastics.

Concentration and distribution of polycyclic aromatic hydrocarbons in oysters from Todos os Santos Bay (Bahia, Brazil).

The aim of the present study was to evaluate the presence of polycyclic aromatic hydrocarbons (PAHs) in oysters (Crassostrea rhizophorae) collected from Todos os Santos Bay (Bahia, Brazil). The total PAH concentration was highest in Madre de Deus (36.3 to 37.8 ng g-1 in dry weight, dw), which is located near a petrochemical complex, oil refinery, and commercial port. In the Paraguaçu river estuary, PAH concentrations varied between 23.2 and 25.7 ng g-1 dw. The lowest concentrations (1.55 ng g-1 dw) were found in the Jaguaribe river estuary, which can be considered a relatively preserved area. The main source of PAHs in the study areas was observed to be pyrogenic. Values of benzo[a]pyrene toxic equivalent ranged from 0.28 to 4.20. The concentrations of PAHs in oysters from the Paraguaçu river estuary and in Madre de Deus indicate the possible lifetime risk of developing cancer in humans who feed on it.

Formation of OSA and dispersion of polycyclic aromatic hydrocarbons in a tropical estuary as a tool in the prevention of environmental impacts: influence of the biogeochemical characteristics of the estuary.

The formation of an oil-suspended particulate material aggregate (OSA) is one of the weathering processes that occur after the spill of oil in marine environments, responsible for the dispersion of hydrocarbons. Oil and particle aggregates are formed from the interaction between small oil droplets and suspended particulate matter (SPM). In general, SPM are fine particles which may be inorganic minerals or organic particles in the water column. OSAs provide vertical dispersion of oil along the water column depending on the acquired density (buoyancy), and may remain near the surface, water column, or bottom of water bodies. The present study examines the formation of these aggregates through the laboratory simulation of an oil spill in the waters of the São Paulo river estuary. The main objective was to investigate the dispersion of polycyclic aromatic hydrocarbons (PAHs), verifying which estuary characteristics most influenced the formation of OSAs and in addition to determine the regions of probable ecotoxicological impact due to the negative buoyancy of the formed aggregate. The results show that there was greater dispersion to the water column, mainly of lighter PAHs, ranging from 85,804.05 ng g-1 (P11C) to 566,989.84 ng g-1 (P17C). The percentage of dispersed PAH concentration per experimental unit ranged from 9.90% in unit P2 to 75.27% in unit P18. The formation of OSAs was influenced mainly by salinity and chlorophyll a. As the most vulnerable regions, the impacts are one mouth (P2 and P4), one central region (P7, P8, and P10), and one source (P18).

Research of OSA seasonal training in the São Paulo River, BTS: a tool to prevent potential ecotoxicological impacts.

Oil exploitation, the basis of the world energy sector, is linked to risks and accidents, causing damage to the affected regions. Oil-suspended particulate matter aggregate (OSA) is a promising technology to mitigate those effects. The present study periodically (February 2016 and July 2016) evaluated the dispersion of oil at 28 points in the São Paulo River's estuary, Todos os Santos Bay, Brazil, analyzing the influence of suspended particulate matter (SPM), particulate organic carbon (POC), ions, and chlorophyll on the formation OSA, targeting the prediction of possible ecotoxicological risks. The results showed that the estuary presented similar characteristics in the expeditions, reflecting the oil dispersion pattern through the formation of OSAs, being 92.86% dispersed in the column in the first and 85.71% in the second expedition. The results also pointed to the possibility of pollution in the food chain, reduced fertility, the emergence of abnormalities and the gradual disappearance of species across the whole river in a possible oil spill.

Speciation analysis of inorganic antimony in sediment samples from São Paulo Estuary, Bahia State, Brazil.

This paper proposes an extraction procedure for the speciation analysis of inorganic antimony in sediment samples using slurry sampling and hydride generation atomic absorption spectrometry. The optimization step of extraction of the species was performed employing a full two-level factorial design (2(3)) and a Box-Behnken matrix where the studied factors in both experiments were: extraction temperature, ultrasonic radiation time, and hydrochloric acid concentration. Using the optimized conditions, antimony species can be extracted in closed system using a 6.0 M hydrochloric acid solution at temperature of 70 °C and an ultrasonic radiation time of 20 min. The determination of antimony is performed in presence of 2.0 M hydrochloric acid solution using HG AAS by external calibration technique with limits of detection and quantification of 5.6 and 19.0 ng L(-1) and a precision expressed as relative standard deviation of 5.6 % for an antimony solution with concentration of 6.0 µg L(-1). The accuracy of the method was confirmed by analysis of two certified reference materials of sediments. For a sample mass of sediment of 0.20 g, the limits of detection and quantification obtained were 0.70 and 2.34 ng g(-1), respectively. During speciation analysis, antimony(III) is determined in presence of citrate, while total antimony is quantified after reduction of antimony(V) to antimony(III) using potassium iodide and ascorbic acid. The method was applied for analysis of six sediment samples collected in São Paulo Estuary (Bahia State, Brazil). The antimony contents obtained varied from 45.3 to 89.1 ng g(-1) for total antimony and of 17.7 to 31.4 ng g(-1) for antimony(III). These values are agreeing with other data reported by the literature for this element in uncontaminated sediment samples.