Radiological Analyses of 226Ra and 238U in Surface Water and Sediments from the Jackpile Member of the Morrison Formation, Pueblo of Laguna, New Mexico.

Surface water and sediments from the Jackpile mine, St. Anthony mine, Rio Paguate, Rio Moquino, and Mesita Dam areas near Pueblo of Laguna, New Mexico, were analyzed for 226Ra and U using gamma (γ) spectroscopy and inductively coupled plasma mass spectroscopy, respectively. Activity ratios for 226Ra/238U for solid samples range from 0.34 ± 0.13 to 16 ± 2.9, which reflect uranium transport and accumulation (<1), relatively pristine material in secular equilibrium (1), and removal of uranium by weathering (>1). Concentrations ranging from 80 to 225 µg L-1 U were detected in unfiltered water samples near the Jackpile mine. Water samples upstream and downstream from the mine contained concentrations ranging from 12 to 15 µg L-1 U. Water samples collected from the North Pit standing pond in the Jackpile mine contained as much as 1560 pCi L-1 of 226Ra, and passing the water through a 0.2 µM filter did not substantially reduce the activity of 226Ra in the water. 234Th and 226Ra are in secular equilibrium in this water, while radon gas was lost from the water. The results of the current study provide insight into the distribution of U-series radionuclides in the Pueblo of Laguna area, including detection of high levels of radioactivity in water at some locations within the Jackpile mine.

Environmental impact assessment due to the intake of uranium contained in surface waters in a semi-arid region in Brazil.

In Santa Quitéria City, part of the population uses surface water for potation. These waters do not undergo any treatment before consumption. As the region has a deposit of uranium, assessing water quality becomes important. In the present study, the uranium activity concentration (AC) in becquerels per liter was determined in water samples from six points. Univariate statistics showed differences between the soluble and the particulate fraction (soluble AC > particulate AC). The particulate fraction showed no variation in AC among the six points. On the other hand, the soluble fraction and the total fraction presented different ACs between them. The multivariate statistics allowed to separate the soluble from the particulate fraction of the points. The same tools applied to the total fraction made it possible to differentiate the sampling points, grouping them ((#1, #2); (#3, #4), and (#5, #6)). The maximum mean value of AC found was 0.177 Bq∙L-1, corresponding to 25% of the chemical toxicity limit (0.72 Bq∙L-1). The maximum mean dose rate, 2.25 µSv∙year-1, is lower than the considered negligible dose rate (> 10 µSv∙year-1). The excess lifetime cancer risk was 10-6, two orders of magnitude smaller than the threshold considered for taking action. The assessment parameters used in this work indicate that the risk due to the uranium intake by the local population is negligible.

Synthesis and Application of a New Polymer with Imprinted Ions for the Preconcentration of Uranium in Natural Water Samples and Determination by Digital Imaging.

This work proposes the synthesis of a new polymer with imprinted ions (IIP) for the pre-concentration of uranium in natural waters using digital imaging as a detection technique. The polymer was synthesized using 2-(5-bromo-2-pyridylazo)-5-diethylaminophenol (Br-PADAP) for complex formation, ethylene glycol dimethacrylate (EGDMA) as a crosslinking reagent, methacrylic acid (AMA) as functional monomer, and 2,2'-azobisisobutyronitrile as a radical initiator. The IIP was characterized by Fourier transform infrared spectroscopy and scanning electron microscopy (FTIR). Uranium determination was performed using digital imaging (ID), and some experimental conditions (sample pH, eluent concentration, and sampling flow rate) were optimized using a two-level full factorial design and Doelhert response surface methodology. Thus, using the optimized conditions, the system allowed the determination of uranium with detection and quantification limits of 2.55 and 8.51 µg L-1, respectively, and a pre-concentration factor of 8.2. All parameters were determined using a 25 mL sample volume. The precision expressed as relative deviation (RSD%) was 3.5% for a solution with a concentration of 50 µg L-1. Given this, the proposed method was used for the determination of uranium in four samples of natural waters collected in the city of Caetité, Bahia, Brazil. The concentrations obtained ranged from 35 to 75.4 µg L-1. The accuracy was evaluated by the addition/recovery test, and the values found ranged between 91 and 109%.

Changes in the oxidative status and damage by non-essential elements in the digestive gland of the gastropod Pomacea canaliculata.

The freshwater gastropod Pomacea canaliculata fulfills the ideal conditions of a bioindicator species since its digestive gland bioconcentrates elements toxic for human and ecosystems health. The aim of this work was to study the balance between production of free radicals and antioxidant defenses, and the generation of oxidative damage in the digestive gland of this mollusk after exposure (96 h) to three elements with differential affinities for functional biological groups: mercury (5.5 µg/L of Hg+2 as HgCl2), arsenic [500 µg/L of (AsO4)-3 as Na3AsO47H2O], or uranium [700 µg/L of (UO2)+2 as UO2(CH2COOH)2]. Bioconcentration factors of Hg, As, and U were 25, 23, and 53, respectively. Snails exhibited a sustained increase of reactive species (RS), and protein and lipid damage. Lipid radicals increased between 72 and 96 h, respectively, in snails exposed to U and Hg while this parameter changed early (24 h) in As- exposed snails. Snails showed protein damage, reaching maximum values at different endpoints. This redox disbalance was partially compensated by non-enzymatic antioxidant defenses α-tocopherol (α-T), ß-carotene (ß-C), uric acid, metallothionein (MTs). Snails consumed α-T and ß-C in an element-dependent manner. The digestive gland consumed rapidly uric acid and this molecule was not recovered at 96 h. Digestive gland showed a significant increase in MTs after elemental exposure at different endpoints. The enzymatic antioxidant defenses, represented by the catalase and glutathione-S-transferase activities, seems to be not necessary for the early stages of the oxidative process by metals. This work is the first attempt to elucidate cellular mechanisms involved in the tolerance of this gastropod to non-essential elements. The bioconcentration factors and changes in the oxidative status and damage confirm that this species can be used as a bioindicator species of metal pollution in freshwater bodies.

Relationship of thorium, uranium isotopes and uranium isotopic ratios with physicochemical parameters in cenote water from the Yucatán Peninsula.

Uranium (U) and Thorium (Th) concentrations are normally low in the water (<30 and 5 ng mL-1, respectively). However, we performed a direct analysis of 232Th, 234U, 235U and 238U in cenote water from the Yucatán Peninsula using Inductively Coupled Plasma Mass Spectrometry (ICP-MS) as a rapid response technique to perform environmental radioactivity monitoring. Water samples were collected in 2021 from the cenotes and these were certificated by zones (PYNO, PYNE and PYSE) and monitoring depth [surface water (n = 52) and depth water (n = 48)]. Moreover, physicochemical parameters such as pH, electrical conductivity (EC), total dissolved solids (TDS), and temperature were measured in situ. Results obtained were total U and Th levels below permissible for human consumption. However, physicochemical parameters must be considered before use because it is outside the permissible limits in most cenotes. The median concentration value for 234U, 235U, 238U and 232Th in surface + depth water were 0.0001 ng mL-1, 0.0130 ng mL-1, 1.76 ng mL-1, and 0.062 ng mL-1, respectively. In addition, isotopic ratio of 235U/238U in surface + depth water was 0.00730. In addition, the PYNO zone showed a correlation between 232Th with EC and TDS. The PYSE zone showed a correlation between 232Th and temperature, and 235U/234U with pH, while PYEN did not show correlations. In conclusion, the first time evaluated U isotope concentrations and isotopic ratios of U and 232Th in cenote water from the Yucatán Peninsula, where U and Th concentrations were found below the permissible limits mentioned by guidelines for drinking-water quality. The average of 235U/238U is similar to isotopic ratios in "natural" water.

Determination of the internal dose due to the intake of 226Ra and 210Pb in drinking water from deep wells in the Metropolitan Region of Recife-Brazil.

The Metropolitan Region of Recife, the capital of the state of Pernambuco in northeastern Brazil, has a high demographic density and developed under a region of marine phosphorus with high concentrations of phosphate that naturally contains uranium ore, producing ionizing radiation from descendants of the radioisotope 238U where 226Ra and 210Pb are of great importance in verifying the probable harmful effects on human health due to environmental radioactivity. The supply of drinking water is the responsibility of the state-owned company COMPESA which uses wells of great depth to complete the supply of drinking water for the entire population. COMPESA and the RAE Group of the Federal University of Pernambuco developed a joint project to assess the concentrations of 226Ra and 210Pb and estimate the equivalent and effective doses caused by ingesting these radiation sources. According to the above, this research aimed to evaluate concentrations of 226Ra and 210Pb in drinking water samples from 110 deep wells in Recife. The activities of 226Ra and 210Pb ranged from 1.4 ± 0.3 to 119.3 ± 12.9 and from 25.6 ± 3.3 to 563.2 ± 45.6 mBq.L-1, with arithmetic means of 48.1 ± 3.8 and 231.1 ± 20 mBq.L-1, respectively. The equivalent doses average in bone tissue due to 226Ra and 210Pb were 0.45 ± 0.04 and 3.9 ± 0.37 mSv.y-1, and the annual average effective doses were 0.01 ± 0.00 and 0.13 ± 0.01 mSv.y-1, respectively.

Biosorption of uranium from aqueous solutions by Azolla sp. and Limnobium laevigatum.

The main goal of this study was to assess alternatives to the current challenges on environmental quality and circular economy. The former is here addressed by the treatment of radioactively contaminated solutions, and the latter by using abundant and low-cost biomass. In this paper, we examine the biosorption of hexavalent uranium (U(VI)) in a batch system using the macrophytes Limnobium laevigatum and Azolla sp. by three operational parameters: biomass dose, metal ion concentration, and contact time. Simulated solutions were firstly addressed with two biomasses, followed by studies with real liquid organic radioactive waste (LORW) with Azolla sp. The batch experiments were carried out by mixing 0.20 g biomass in 10 mL of the prepared solution or LORW. The total contact time employed for the determination of the equilibrium times was 240 min, and the initial U(VI) concentration was 0.63 mmol L-1. The equilibrium times were 15 min for L. laevigatum and 30 min for Azolla sp. respectively. A wide range of initial U(VI) concentrations (0.25-36 mmol L-1) was then used to assess the adsorption capacity of each macrophyte. Isotherm models validated the adsorption performance of the biosorption process. Azolla sp. presented a much higher U(VI) uptake (0.474 mmol g-1) compared to L. laevigatum (0.026 mmol g-1). When in contact with LORW, Azolla sp. removed much less uranium, indicating an adsorption capacity of 0.010 mmol g-1. In conclusion, both biomasses, especially Azolla sp., can be used in the treatment of uranium-contaminated solutions.

Talaromyces amestolkiae uses organic phosphate sources for the treatment of uranium-contaminated water.

Fungi have received particular attention in regards to alternatives for bioremediation of heavy metal contaminated locales. Enzymes produced by filamentous fungi, such as phosphatases, can precipitate heavy metal ions in contaminated environments, forming metal phosphates (insoluble). Thus, this research aimed to analyze fungi for uranium biomineralization capacity. For this, Gongronella butleri, Penicillium piscarium, Rhodotorula sinensis and Talaromyces amestolkiae were evaluated. Phytate and glycerol 2-phosphate were used as the phosphate sources in the culture media at pH 3.5 and 5.5, with and without uranium ions. After 4 weeks of fungal growth, evaluated fungi were able to produce high concentrations of phosphates in the media. T. amestolkiae was the best phosphate producer, using phytate as an organic source. During fungal growth, there was no change in pH level of the culture medium. After 3 weeks of T. amestolkiae growth in medium supplemented with phytate, there was a reduction between 20 and 30% of uranium concentrations, with high precipitation of uranium and phosphate on the fungal biomass. The fungi analyzed in this research can use the phytic acid present in the medium and produce high concentrations of phosphate; which, in the environment, can assist in the heavy metal biomineralization processes, even in acidic environments. Such metabolic capabilities of fungi can be useful in decontaminating uranium-contaminated environments.

Naturally-Occurring Radioactive Materials at water treatment plant on the Poços de Caldas Plateau Region, Brazil / Materiais Radioativos de Ocorrência Natural em estações de tratamento de água no Planalto de Poços de Caldas, Brasil

ABSTRACT Oil and gas, mining, among others, are examples of facilities where naturally occurring radioactive materials can be found. This study aims to evaluate the presence of natural radioactive series, especially those of 238U and 232Th, in the water treatment plants of Poços de Caldas City, Minas Gerais. The presence of these series was investigated in samples of raw water, treated water, sludge from decanters, and scale from Parshall gutters. The sludge, input, and scale samples were submitted to the gamma spectrometry technique to determine the 226Ra, 228Ra, and 210Pb radionuclides. For U and Th, ultraviolet visible spectrophotometry was performed, and for the alpha and beta total values, radiochemical separation and subsequent alpha and beta total counts were performed. The results indicate that water samples are within the Ministry of Health Ordinance n° 5 (2017). Due to the different concentrations of radionuclide activity in the sludge, it was not possible to affirm the same order of magnitude with the sediment from the catchments. However, the values are in accordance with those established by the European Union Council for Naturally-Occurring Radioactive Materials. In the scale, the contents of 1192, 1704, and 301 Bq kg−1 were identified for 226Ra, 228Ra, and 210Pb, respectively. In the inputs of aluminum sulfate and calcium hydroxide, no relevant activities were identified. The results obtained in the study can serve as an indicative regarding the need for a more detailed evaluation of the radiological issue in question concerning public water supplies.

RESUMO Petróleo e gás, mineração, estações de tratamento de água, entre outros, são exemplos de instalações que podem apresentar Materiais Radioativos de Ocorrência Natural. Neste estudo, objetivou-se avaliar a presença de séries radioativas naturais, especialmente as de 238U e 232Th nas estações de tratamento de água da cidade de Poços de Caldas/MG. Foram investigadas as presenças dessas séries em amostras de água bruta, de água tratada, no lodo dos decantadores e nas incrustações das calhas Parshall, além dos principais insumos utilizados. As amostras de lodo, insumos e incrustações foram submetidas à técnica de espectrometria gama para a determinação dos radionuclídeos 226Ra, 228Ra e 210Pb. Para U e Th, realizou-se espectrofotometria ultravioleta-visível, e para os valores de Alfa e Beta totais foram realizadas separação radioquímica e posterior contagem Alfa e Beta total. Os resultados indicaram que as amostras de águas estão em conformidade com a Portaria de Consolidação n° 5 de 2017 do Ministério da Saúde. Dadas as diferentes concentrações de atividade dos radionuclídeos no lodo, não foi possível afirmar a mesma ordem de magnitude com o sedimento das captações. Entretanto, os valores estão consonantes com o estabelecido pelo conselho da União Europeia para Materiais Radioativos de Ocorrência Natural. Nas incrustações foram identificados teores de 1.192 Bq.kg-1, 1.704 Bq.kg-1 e 301 Bq.kg-1 para 226Ra, 228Ra e 210Pb, respetivamente. Já para os insumos Sulfato de Alumínio (Al4(SO4)3) e Hidróxido de Cálcio Ca(OH)2 não foram identificadas atividades relevantes. Os resultados obtidos no estudo podem servir como indicativos da necessidade de uma avaliação mais detalhada sobre a questão radiológica em foco, em relação ao abastecimento público de águas.

Lifetime cancer risk increase due to consumption of some foods from a High Background Radiation Area.

Activity concentration (AC) in foods produced and commonly consumed in a High Background Radiation Area (HBRA) was analyzed. The AC were obtained by spectrophotometry and by the radiochemical separation method. The AC were up to 104 times higher than the AC for both UNSCEAR suggested values and non-HBRA. It was noted that the lifetime cancer risk was increased in 4 decimal places, taking the risk from the "statistically negligible range" (<10-6) to "middle range" (between 10-4 and 10-6).

Lability and bioavailability of Co, Fe, Pb, U and Zn in a uranium mining restoration site using DGT and phytoscreening.

Mine restoration is a long and ongoing process, requiring careful management, which must be informed by site-specific, geochemical risk assessment. Paired topsoil and tree core samples from 4 sites within the uranium mining complex of INB Caldas in Minas Gerais (Brazil) were collected. Soil samples were analysed for their total content of Co, Fe, Pb, U and Zn by XRF, and subsequently, the potential environmental bioavailability of these metals were investigated by DGT and pore water analysis. In addition, results were compared with metal concentrations obtained by Tree Coring from the forest vegetation. In all sampling areas, mean total concentrations of U (Ctot. = 100.5 ± 66.5 to 129.6 ± 57.1 mg kg-1), Pb (Ctot. = 30.8 ± 12.7 to 90.8 ± 90.8 mg kg-1), Zn (Ctot. = 91.5 ± 24.7 to 99.6 ± 10.3 mg kg-1) and Co (Ctot. = 73.8 ± 25.5 to 119.7 ± 26.4 mg kg-1) in soils exceeded respective quality reference values. Study results suggest that AMD caused the increase of labile concentrations of Zn in affected soils. The high lability of the elements Pb (R = 62 ± 34 to 81 ± 29%), U (R = 57 ± 20 to 77 ± 28%) and Zn (R = 21 ± 25 to 34 ± 31%) in soils together with high bioconcentration factors found in wood samples for Pb (BCF = 0.0004 ± 0.0003 to 0.0026 ± 0.0033) and Zn (BCF = 0.012 ± 0.013 to 0.025 ± 0.021) indicated a high toxic potential of these elements to the biota in the soils of the study site. The combination of pore water and DGT analysis with Tree Coring showed to be a useful approach to specify the risk of metal polluted soils. However, the comparison of the results from DGT and Tree Coring could not predict the uptake of metals into the xylems of the sampled tree individuals.

Highly efficient adsorption and immobilization of U(VI) from aqueous solution by alkalized MXene-supported nanoscale zero-valent iron.

A novel composite of zero-valent iron nanoparticles supported on alkalized Ti3C2Tx nanoflakes (nZVI/Alk-Ti3C2Tx) was constructed by an in-situ growth method for simultaneous adsorption and reduction U(VI) from aqueous solution in anoxic conditions. The effect of various factors such as adsorbent dose, pH, ionic strength, contact time, initial U(VI) concentration and environmental media were comprehensively investigated by batch experiments. Benefiting from the good dispersion uniformity of nZVI on MXene substrates, nZVI/Alk-Ti3C2Tx exhibited rapid removal kinetics, excellent selectivity, 100% removal efficiency and up to 1315 mg g-1 uptake capacity for U(VI) capture. In the presence of mimic groundwater, 1.0 mM NaHCO3 and 10 mg L-1 humic acid, the removal percentages of U(VI) by the composites could reach 95.1%, 88.9% and 69.5%, respectively. The reaction mechanism between U(VI) and nZVI/Alk-Ti3C2Tx has been clarified based on FTIR, XANES, XPS and XRD analysis. Depending on the consumption of reactive nZVI in the composites and the solution pH, the elimination of U(VI) could be realized by different pathways including reductive immobilization in the form of UO2, inner-sphere surface complexation and hydrolysis precipitation. The present study illustrates that the nZVI/Alk-Ti3C2Tx composite may be an efficient scavenger for radioactive wastewater purification in environmental remediation.

A toxicological comparison between two uranium compounds in Artemia salina: Artificial seawater containing CaCO3.

Uranium (U) mining is an aquatic environmental concern because most of these harmful compounds are discharged into freshwater, reaching the saline environment as the final destination of this contaminated water. Carbonates are present in ocean waters and are essential for benthic organisms, however they may influence the U-induced toxicity. Thus, the aim of this study was to compare the toxicity of uranium nitrate (UN) and uranium acetate (UA) in Artemia salina (AS), which is one of the leading representatives of the marine biota. The cultures of AS (instar II) maintained in artificial seawater containing CaCO3 were exposed for 24 h to different concentrations of U compounds. The results showed that AS were more sensitive to UN (LC50 ≈ 15 µM) when compared with UA (LC50 ≈ 245 µM) indicating higher toxicity of this U compound. Calculated U speciation indicated that Ca2UO2(CO3)3 and (UO2)2CO3(OH)3- complexes predominated under our experimental conditions. The immobilization/lethality was observed after 9 h of exposure for both U compounds. However, only UN caused a significant decrease (≈40%) in the acetylcholinesterase (AChE) activity when compared with control. In order to observe preliminary toxicity effects, we evaluated oxidative stress parameters, such as catalase (CAT) activity, TBARS formation, radical species (RS) generation and cell membrane injury and/or apoptosis (CMI). In this study, we demonstrate that U compounds caused a significant decrease in CAT activity. Similarly, we also observed that UN increased TBARS levels in AS at concentrations 5 times lower than AU (10 µM and 50 µM, respectively). Furthermore, RS generation and CMI were enhanced only on AS treated with UN. Overall, the effects observed here were remarkably significant in AS exposed to UN when compared with AU. In this study, we showed different profiles of toxicity for both U compounds, contributing significantly to the current and scarce understanding of the aquatic ecotoxicity of this heavy metal.

Bioaccumulation of potentially toxic elements from the soils surrounding a legacy uranium mine in Brazil.

It is important to understand the environmental fate and potential risks posed by metals and metalloids around mines and in legacy mining areas. In order to assess the bioavailable concentrations of several potentially toxic elements (PTEs: As, Pb, Cd, Ni, Cu, Cr, Mn, Zn, Ba, U) and rare earth elements (REEs: La to Lu), a multi-method evaluation of their concentrations/fractionation/speciation in soils was related to their biouptake in corn, for a region surrounding a legacy U mine in Brazil. Chemical fractions of the PTE and REE in soils were determined using the BCR (Community Bureau of Reference) sequential extraction procedure; a single extraction with Ca(NO3)2 and the diffusion gradient in thin films (DGT) technique. All techniques were better correlated to the metals accumulated by the crops as compared to total metal concentrations. Ba, Cu, Mn and Zn were shown to have high mobility and high bioaccumulation factors in the corn. Concentrations of U, As, Cd, and Pb were above threshold concentrations and strongly correlated, suggesting that they had a similar anthropogenic source. Geospatial modeling agreed with results from principal component analysis, indicating multiple sources for the contamination. Results highlighted the need for multi-method approaches when evaluating the long-term risks posed by PTEs and REEs in agricultural soils.

Environmental and health risk assessment of agricultural areas adjacent to uranium ore fields in Brazil.

To investigate the risks posed by trace and rare earth elements (REEs) in two tropical uranium ore fields, metal concentrations from 50 vegetable samples (corn and soybean) and their corresponding agricultural soils were evaluated in a U mining area and a U-rich coal mining area in Brazil. Samples from both areas had metal concentrations (REE: La to Lu, and trace elements: As, Pb, Cd, Ni, Cu, Cr, Mn, Zn, Ba, U, Sr) that were higher than the guidelines proposed by the Brazilian environmental agency. Soils from the U mining area (Poços de Caldas) generally had higher contents of trace elements than the coal mining area (Figueira), with the exception of Ni and Cr, indicating a higher risk of pollution, which was confirmed by a pollution load index that was greater than unity. For both sites, concentrations of uranium in the soil and plants, its hazard quotients and the soil contamination factor were higher in agricultural fields closer to the mines, indicating that contamination and the consequent risks to human health were distance dependent. REE concentrations averaged 52.8 mg kg-1 in the topsoils and 0.76 mg kg-1 in the grains for Figueira, whereas higher values of 371 mg kg-1 (topsoils) and 0.9 mg kg-1 (grains) were found in Poços de Caldas. Based upon corn and soybean consumption, the estimated intake dose of the REE was lower than the intake dose predicted to be problematic for human health for both sites, indicating limited risk related to the ingestion of REE.

Evaluation of the radiological quality of water released by a uranium mining in Brazil.

A mine in an area of naturally occurring radioactive materials (NORM), characterized by acid mine drainage, generates effluents with natural radionuclide concentrations, usually above the limits authorized by the regulator. The plant exploiting NORM controls the water quality and discharges it into the aquatic environment after meeting technical requirements. Downstream, water usage is unrestricted. In order to reach activity concentrations in the released effluents below the authorized values, the facility applies a chemical treatment to the effluent. Then, to ensure the effectiveness of the treatment, the facility performs sampling of treated effluent and determines the activity concentration of natural radionuclides (Unat, 226Ra, and 210Pb from the uranium series and 232Th and 228Ra from the thorium series). In the current study, the proportion and distribution of these radionuclides between the soluble and particulate fractions were determined. The measured activity concentrations were compared with the values proposed by the World Health Organization and Brazilian legislation, as well as other authorities, as regards the potable use from the radioprotection point of view. It was observed that the radionuclides are not in secular equilibrium. The fractions contribute differently to the total release of radionuclide, and there is no linear relationship between the fractions. The average activity concentrations did not result in radiological restrictions to water use, and the committed effective dose due to ingestion was estimated at 0.06 mSv y-1. Therefore, there is no radiological restriction to water use, since the dose which was found was below the constraint value for the public.

Bioremediation of water contaminated with uranium using Penicillium piscarium.

Penicillium piscarium can be indicated as promising in the treatment of sites contaminated with uranium. Thus, this research aimed to analyze the P. piscarium dead biomass in uranium biosorption. This fungus was previously isolated from a highly contaminated uranium mine located in Brazil. Biosorption tests were carried out at pH 3.5 and 5.5 in solutions contaminated with concentrations of 1 to 100 mg/L of uranium nitrate. Our results showed that the dead biomass of P. piscarium was able to remove between 93.2 and 97.5% uranium from solutions at pH 3.5, at the end of the experiment, the pH of the solution increased to values above 5.6. Regarding the experiments carried out in solutions with pH 5.5, the dead biomass of the fungus was also able to remove between 38 and 92% uranium from the solution, at the end of the experiment, the pH of the solution increased to levels above 6.5. The analysis of electron microscopy, Energy-dispersive spectroscopy, and X-ray fluorescence demonstrated the high concentration of uranium precipitated on the surface of the fungal biomass. These results were impressive and demonstrate that the dead biomass of P. piscarium can be an important alternative to conventional processes for treating water contaminated with heavy metals, and we hope that these ecofriendly, inexpensive, and effective technologies be encouraged for the safe discharge of water from industrial activities.

The use of rice and coffee husks for biosorption of U (total), 241Am, and 137Cs in radioactive liquid organic waste.

Rice and coffee husks (raw and chemically activated) are examined as potential biosorption materials regarding their capacity to remove U (total), 241Am, and 137Cs. The physical parameters evaluated were the morphological characteristics of the biomass, real and apparent density, and surface area. Contact times for the batch experiments were 0.5, 1, 2, and 4 h, and the concentrations tested ranged between 10% of the total concentration and the radioactive waste itself without any dilution. The results were evaluated by experimental sorption capacity, ternary isotherm, and kinetics models. The kinetics results showed that equilibrium was reached after 2 h for all biomass. Raw coffee husk showed the best adsorption results in terms of maximum capacity (qmax) for all three radionuclides, which were 1.96, 39.4 × 10-6, and 46.6 × 10-9 mg g-1 for U, Am, and Cs, respectively. The biosorption process for the raw and activated rice husks was best represented by the Langmuir ternary isotherm model with two sites. For the coffee husk, in the raw and activated states, the biosorption process was best described by the modified Jain and Snoeyink ternary model. These results suggest that biosorption with these biomaterials can be applied in the treatment of liquid organic radioactive waste containing mainly uranium and americium.

A mineração de urânio em questão: análise da comunicação pública das Indústrias Nucleares do Brasil (INB) em Caetité, Bahia / Questioning uranium mining: an analysis of the public communication stated by Indústrias Nucleares do Brasil (INB) in Caetité, Bahia / La minería de uranio en cuestión: un análisis de la comunicación pública transmitida por la INB (Indústrias Nucleares do Brasil) en Caetité, Bahia

O objetivo deste artigo é discutir, através de análise de conteúdo, as estratégias de comunicação pública adotadas pelas Indústrias Nucleares do Brasil no 'Espaço INB', um centro de informações localizado na cidade baiana de Caetité, onde a empresa realiza a mineração e o beneficiamento de urânio. Desde que foram iniciadas, essas atividades levantaram inúmeras suspeitas de danos ambientais e problemas de saúde pública. Diante disso, buscamos compreender como a INB se posiciona diante dessas suspeitas e se relaciona com as populações atingidas por suas atividades. De acordo com nosso argumento, ao adotar uma postura que denominamos tecnoentusiasta e tecnocrática, a empresa dificulta um debate público aberto e descentralizado sobre as controvérsias em torno da mineração de urânio

This article aims to use the content analysis to discuss the public communication stated by the 'Espaço INB', an information center managed by Indústrias Nucleares do Brasil located in the city of Caetité ­ BA, where the company mines and processes uranium. Since INB started its activities in Caetité, several suspicions of environmental damage and public health problems emerged. Thus, we analyze how INB responds to these suspicions and relates to the populations affected by its activities. We argue that INB adopts an attitude that we call techno-enthusiastic and technocratic, hindering an open public and decentralized debate about the controversies surrounding uranium mining.

El objetivo de este artículo es discutir, a través del análisis de contenido, la comunicación pública transmitida por el 'Espaço INB', un centro de información administrado por Indústrias Nucleares do Brasil ubicado en la ciudad de Caetité/Bahia, donde la empresa hace la mínería y el procesamiento del uranio. Desde que comenzaron, estas actividades han generado numerosas sospechas de daños ambientales y problemas de salud pública. Por eso, analizamos como el INB contesta estas sospechas y se relaciona con las poblaciones afectadas por sus actividades. Argumentamos que el INB adopta una actitud que llamamos tecno-entusiasta y tecnocrática, lo que dificulta un debate público abierto y descentralizado sobre las controversias respecto a la minería de uranio.

Resistant fungi isolated from contaminated uranium mine in Brazil shows a high capacity to uptake uranium from water.

The Osamu Utsumi uranium mine occupies a 20 km2 area in the city of Caldas, which is located in the state of Minas Gerais, Brazil. Since mining activities ended at Osamu Utsumi 24 years ago, the surrounding area has become contaminated by acid effluents containing high concentrations of uranium. Thus, the aim of this study was to assess the uranium bioremediation capacity of 57 fungi isolated from the mine area. In tolerance tests, 38% (22) of the fungal isolates were considered tolerant to uranium, including 10 Penicillium species. At a uranium concentration of 2000 mg L-1 48 fungi did not exhibit mycelial growth index inhibition. Minimal inhibitory concentration (MIC) analysis showed growth of 25 fungi above a uranium concentration of 8000 mg L-1. At high uranium concentrations, some fungi (i.e., Talaromyces amestolkiae and Penicillium citrinum) showed morphological changes and pigment (melanin) production. Among the fungal isolates, those considered to be more tolerant to uranium were isolated from soil and sediment samples containing higher concentrations of heavy metal. When comparing the results of resistance/tolerance tests with those for uranium biosorption capacity, we concluded that the fungi isolated from the Osamu Utsumi mine with the best potential for uranium bioremediation were Gongronella butleri, Penicillium piscarium, Penicillium citrinum, Penicillium ludwigii, and Talaromyces amestolkiae. Biosorption tests with live fungal biomass showed that 11 species had a high potential for uranium uptake from contaminated water.