RESUMEN
Thorium biosorption by a green microalga, Chlorella Vulgaris, was studied in a stirred batch reactor to investigate the effect of initial solution pH, metal ion concentration, biomass dosage, contact time, kinetics, equilibrium and thermodynamics of uptake. The green microalgae showed the highest Th adsorption capacity at 45 °C for the solution with a thorium concentration of 350 mg L-1 and initial pH of 4. The amount of uptake raised from 84 to 104 mg g-1 as the temperature increased from 15 to 45 °C for an initial metal concentration of 75 mg L-1 at pH 4. Transformation Infrared Spectroscopy (FTIR) was employed to characterize the vibrational frequency changes for peaks related to surface functional groups. Also, the scanning electron microscope (SEM) and energy-dispersive X-ray spectroscopy (EDX) were used to determine the morphological changes and elemental analysis of the biosorbent before and after the sorption process. The Langmuir isotherm was in perfect agreement with the equilibrium empirical data of thorium biosorption and the highest sorption capacity of the Chlorella Vulgaris microalgae was determined as 185.19 mg g-1. Also, the results of kinetic studies show that the thorium biosorption process follows a pseudo-second-order kinetic model. The negative value of ΔG0 indicates spontaneity and the positive values of ΔH0 indicate the endothermic nature of the adsorption process.
Asunto(s)
Chlorella vulgaris , Microalgas , Torio , Chlorella vulgaris/metabolismo , Torio/metabolismo , Torio/química , Adsorción , Microalgas/metabolismo , Cinética , Concentración de Iones de Hidrógeno , Biomasa , Termodinámica , Espectroscopía Infrarroja por Transformada de Fourier , Temperatura , Agua/químicaRESUMEN
Thorium is a byproduct of the rare earth mining industry and can be utilized as fuel for the next-generation nuclear power facilities, which may pose health risks to the population. Although published literature has shown that the toxicity of thorium possibly originates from its interactions with iron/heme-containing proteins, the underlying mechanisms are still largely unclear. Since the liver plays an irreplaceable role in iron and heme metabolism in the body, it is essential to investigate how thorium affects iron and heme homeostasis in hepatocytes. In this study, we first assessed the liver injury in mice exposed to tetravalent thorium (Th(IV)) in the form of thorium nitrite via the oral route. After a two-week oral exposure, thorium accumulation and iron overload were observed in the liver, which are both closely associated with lipid peroxidation and cell death. Transcriptomics analysis revealed that ferroptosis, which has not previously been documented in cells for actinides, is the main mechanism of programmed cell death induced by Th(IV). Further mechanistic studies suggested that Th(IV) could activate the ferroptotic pathway through disrupting iron homeostasis and generating lipid peroxides. More significantly, the disorder of heme metabolism, which is crucial for maintaining intracellular iron and redox homeostasis, was found to contribute to ferroptosis in hepatocytes exposed to Th(IV). Our findings may shed light on a key mechanism of hepatoxicity in response to Th(IV) stress and provide in-depth understanding of the health risk of thorium.
Asunto(s)
Ferroptosis , Ratones , Animales , Torio/metabolismo , Hígado/metabolismo , Hierro/metabolismo , Peroxidación de Lípido , Hemo/metabolismo , Homeostasis , Ingestión de AlimentosRESUMEN
Thorium, as an important radioactive element, is widely present in nature, and its accompanying environmental pollution is also serious. Extracellular polymeric substances (EPS) are commonly found on the surface of microbial bodies and have strong adsorption capacity for metal ions. In this study, four methods were used to extract EPS from indigenous bacteria of rare earth tailings and to determine the best extraction method. The extracted EPS was applied to treat Th4+, and the changes in functional groups and composition of EPS were investigated. The results showed that the ultrasonic method was more efficient than other methods. The best removal efficiency was observed at pH 3.5, Th4+ concentration of 20 mg/L, and EPS dosage of 30 mL at 25 °C. After 9 h, the adsorption process reached equilibrium with a maximum removal efficiency of 75.93% and a maximum theoretical adsorption capacity of 25.96 mg/g. The Th4+ removal process was consistent with the Langmuir and Freundlich adsorption isotherms and the kinetic data were consistent with the pseudo-second-order kinetic model, which is mainly based on chemisorption. Amide I and amide II of proteins, C-H from aliphatic, as well as O-H and C = O from carboxylic acid play important roles in the adsorption process.
Asunto(s)
Matriz Extracelular de Sustancias Poliméricas , Torio , Torio/análisis , Torio/metabolismo , Matriz Extracelular de Sustancias Poliméricas/química , Matriz Extracelular de Sustancias Poliméricas/metabolismo , Bacterias , Iones/análisis , AdsorciónRESUMEN
Ferritin is the main protein of Fe storage in eukaryote and prokaryote cells. It is a large multifunctional, multi-subunit protein consisting of heavy H and light L subunits. In the field of nuclear toxicology, it has been suggested that some actinide elements, such as thorium and plutonium at oxidation state +IV, have a comparable `biochemistry' to iron at oxidation state +III owing to their very high tendency for hydrolysis and somewhat comparable ionic radii. Therefore, the possible mechanisms of interaction of such actinide elements with the Fe storage protein is a fundamental question of bio-actinidic chemistry. We recently described the complexation of Pu(IV) and Th(IV) with horse spleen ferritin (composed mainly of L subunits). In this article, we bring another viewpoint to this question by further combining modeling with our previous EXAFS data for Pu(IV) and Th(IV). As a result, the interaction between the L subunits and both actinides appears to be non-specific but driven only by the density of the presence of Asp and Glu residues on the protein shell. The formation of an oxyhydroxide Th or Pu core has not been observed under the experimental conditions here, nor the interaction of Th or Pu with the ferric oxyhydroxide core.
Asunto(s)
Elementos de Series Actinoides , Plutonio , Elementos de Series Actinoides/metabolismo , Animales , Compuestos Férricos , Ferritinas , Caballos , Plutonio/metabolismo , Torio/metabolismoRESUMEN
Thorium is a radioactive heavy metal and an emerging environmental pollutant. Ecological and human health risks from thorium exposure are growing with the excavation of rare earth metals and implementation of thorium-based nuclear reactors. Thorium poisoning is associated with carcinogenesis, liver impairments, and congenital anomalies. To date, the biomolecular targets that underlie thorium-induced toxicity remain unknown. Here, we used in vitro enzymatic activity assays to comprehensively evaluate the effects of thorium on the mitochondrial respiration process. Thorium was found to inhibit respiratory chain complex IV (cytochrome c oxidase) at sub-micromolar concentrations (IC50 ~ 0.4 µM, 90 µg/L). This is lower than the thorium level limit (246 µg/L) in drinking water specified by the World Health Organization. The inhibitory effects were further verified in mitochondria from human bone and liver cells (thorium mainly deposits in these organs). The inhibition of cytochrome c oxidase can readily rationalize well-documented cellular toxicities of thorium, such as alteration of mitochondrial membrane potential and production of reactive oxygen species. Therefore, cytochrome c oxidase is potentially a key molecular target underlying thorium-induced toxicological effect.
Asunto(s)
Complejo IV de Transporte de Electrones , Torio , Transporte de Electrón , Complejo IV de Transporte de Electrones/metabolismo , Humanos , Potencial de la Membrana Mitocondrial , Mitocondrias/metabolismo , Torio/metabolismoRESUMEN
Two novel extraction chromatography resins (ECRs) containing two diglycolamide (DGA) -functionalized calix[4]arenes with n-propyl and isopentyl substituents at the amide nitrogen atom, termed as ECR-1 and ECR-2, respectively, were evaluated for the uptake of Th(IV) from nitric acid feed solutions. While both the resins were having a quite high Th(IV) uptake ability (Kd >3000 at 3 M HNO3), the uptake was relatively lower with the resin containing the isopentyl DGA, which appeared magnified at lower nitric acid concentrations. Kinetic modeling of the sorption data suggested fitting to the pseudo-second order model pointing to a chemical reaction during the uptake of the metal ion. Sorption isotherm studies were carried out showing a good fitting to the Langmuir and D-R isotherm models, suggesting the uptake conforming to monolayer sorption and a chemisorption model. Glass columns with a bed volume of ca. 2.5 mL containing ca. 0.5 g lots of the ECRs were used for studies to assess the possibility of actual applications of the ECRs. Breakthrough profiles obtained with feed containing 0.7 g/L Th(NO3)3 solution resulted in breakthrough volumes of 8 and 5 mL, respectively, for the ECR-1 and ECR-2 resins. Near quantitative elution of the loaded metal ion was possible using a solution of oxalic acid and nitric acid. A method for the separation of Th-234 from natural uranium was demonstrated for the possible application of ECR-1.
Asunto(s)
Técnicas de Química Analítica , Torio , Uranio , Técnicas de Química Analítica/métodos , Cromatografía/métodos , Cinética , Ácido Nítrico/química , Torio/aislamiento & purificación , Torio/metabolismo , Uranio/aislamiento & purificaciónRESUMEN
The iron carrier human serum transferrin (sTf) is known to transport other metals, including some actinides (An). Radiotoxic An are routinely involved in the nuclear fuel cycle and the possibility of their accidental exposure cannot be ruled out. Understanding An interaction with sTf assumes a greater significance for the development of safe and efficacious chelators for their removal from the blood stream. Here we report several 100 ns equilibrium MD simulations of Cm(III)- and Th(IV)-loaded sTf at various protonation states of the protein to explore the possibility of the two An ions release and speciation. The results demonstrate variation in protonation state of dilysine pair (K206 and K296) and the tyrosine (Y188) residue is necessary for the opening of Cm(III)-bound protein and the release of the ion. For the tetravalent thorium, protonation of dilysine pair suffices to cause conformational changes of protein. However, in none of the protonation states, Th(IV) releases from sTf because of its strong electrostatic interaction with D63 in the first shell of the sTf binding cleft. Analysis of hydrogen bond, water bridge, and the evaluation of potential of mean forces of the An ions' release from sTf, substantiate the differential behavior of Cm(III) and Th(IV) at endosomal pH. The results provide insight in the regulation of Cm(III) and Th(IV) bioavailability that may prove useful for effective design of their decorporating agents and as well may help the future design of radiotherapy based on tetravalent ions.
Asunto(s)
Curio/química , Simulación de Dinámica Molecular , Torio/química , Transferrina/química , Ácido Aspártico/química , Ácido Aspártico/metabolismo , Sitios de Unión , Curio/metabolismo , Endosomas/metabolismo , Humanos , Enlace de Hidrógeno , Concentración de Iones de Hidrógeno , Lisina/química , Lisina/metabolismo , Unión Proteica , Conformación Proteica , Dominios y Motivos de Interacción de Proteínas , Protones , Electricidad Estática , Termodinámica , Torio/metabolismo , Transferrina/metabolismo , Tirosina/química , Tirosina/metabolismoRESUMEN
The impact of the contamination of living organisms by actinide elements has been a constant subject of attention since the 1950s. But to date still little is understood. Ferritin is the major storage and regulation protein of iron in many organisms, it consists of a protein ring and a ferrihydric core at the center. This work sheds light on the interactions of early actinides (Th, Pu) at oxidation state +IV with ferritin and its ability to store those elements at physiological pH compared to Fe. The ferritin-thorium load curve suggests that ThIV saturates the protein (2840 Th atoms per ferritin) in a similar way that Fe does on the protein ring. Complementary spectroscopic techniques (spectrophotometry, infrared spectroscopy, and X-ray absorption spectroscopy) were combined with molecular dynamics to provide a structural model of the interaction of ThIV and PuIV with ferritin. Comparison of spectroscopic data together with MD calculations suggests that ThIV and PuIV are complexed mainly on the protein ring and not on the ferrihydric core. Indeed from XAS data, there is no evidence of Fe neighbors in the Th and Pu environments. On the other hand, carboxylates from amino acids of the protein ring and a possible additional carbonate anion are shaping the cation coordination spheres. This thorough description from a molecular view point of ThIV and PuIV interaction with ferritin, an essential iron storage protein, is a cornerstone in comprehensive nuclear toxicology.
Asunto(s)
Ferritinas/química , Ferritinas/metabolismo , Hierro/metabolismo , Plutonio/metabolismo , Torio/metabolismo , Animales , Caballos , Plutonio/química , Torio/químicaRESUMEN
Selective enriching low content of radionuclides from radioactive wastewater is a critical issue for environmentally benign utilization of nuclear power. Inspired by the tolerance mechanism of plants to radionuclides, we developed a pH-triggered ultraselective coordinative adsorption (CA) membrane. The as-prepared CA membrane featured the advantages of both coordinative adsorption and membrane separation, including ultrahigh selectivity coefficient of 1242, large capacity (80 L m-2) and short mass transfer distance. The adsorption isotherms of Th4+ on the CA membrane were well described by the Freundlich model (R2 > 0.99), and the adsorption kinetics have a good fitting by using the pseudo-second-order kinetic model (R2 > 0.99). In a continuous separation under gravity, the CA membrane was able to selectively enrich the low content of Th4+ (0.05 mmol L-1) in the presence of 700 folds (35 mmol L-1) of co-existing ions (Na+, Mg2+, K+, Ca2+, Sr2+, Cs+ and Ba2+). The exceptional extraction efficiency to Th4+ was 100%, superior to that (3.7%) of all co-existing ions. Notably, the Th4+ enriched on the CA membrane was facilely eluted by diluted HNO3 (0.1 mol L-1). The Th4+ in the eluents was enriched by up to 54 folds. The eluted CA membrane was further reused for selective enrichment of Th4+, which showed no obvious loss of selectivity and enrichment capability. Our strategy might open up a new strategy for realizing ultraselective and recyclable enrichment of low content of irradiation contaminants from wastewater.
Asunto(s)
Adaptación Fisiológica , Fenómenos Fisiológicos de las Plantas , Torio/metabolismo , Membranas Artificiales , Taninos/metabolismo , Torio/análisisRESUMEN
The transfer factors (TFs) of naturally occurring radionuclides, 238U and 232Th from soil to different cassava plant compartments were calculated. Cassava is widely cultivated in Nigeria and contributes significantly to the food supply of the nation. There is sparsity of data on the TFs in Nigeria, and no TF data from any African country were included in the International Atomic Energy Agency's compilation of TFs for the tropical ecosystem. Samples of tin tailings and soil samples from virgin land were used to formulate three soil groups; group-A (soil from virgin land only), group-B (tailings only) and group-C (equal dry mass combination of tailings and soil from virgin land). Pot experiments were set up to determine the TFs of 238U and 232Th. The activity concentrations of 238U and 232Th in the dried samples of the soil and plant compartments were determined using a sodium iodide detector. The TF of 238U ranged from below detection limit (BDL) to 0.01 in the tuber samples, BDL to 0.23 in the stem samples and BDL to 0.90 in the leaf samples, while the TF of 232Th ranged between 0.006 and 0.49 for tuber samples, 0.03 and 0.65 in stem samples and 0.03 and 1.54 in the leaf samples. There were significant difference in the TF of 238U and 232Th between the soil groups. The leaf compartment generally had most of the highest TF values while the tuber samples had most of the lowest TF values for both radionuclides.
Asunto(s)
Manihot/metabolismo , Contaminantes Radiactivos del Suelo/metabolismo , Torio/metabolismo , Uranio/metabolismo , Minería , Nigeria , Hojas de la Planta/metabolismo , Tallos de la Planta/metabolismo , Tubérculos de la Planta/metabolismoRESUMEN
During civil, nuclear or defense activities, internal contamination of actinides in humans and mitigation of their toxic impacts are of serious concern. Considering the health hazards of thorium (Th) internalization, an attempt was made to examine the potential of ten rationally-selected compounds/formulations to decorporate Th ions from physiological systems. The Th-induced hemolysis assay with human erythrocytes revealed good potential of tiron, silibin (SLB), phytic acid (PA) and Liv.52® (L52) for Th decorporation, in comparison to diethylenetriaminepentaacetic acid, an FDA-approved decorporation drug. This was further validated by decorporation experiments with relevant human cell models (erythrocytes and liver cells) and biological fluid (blood) under pre-/post-treatment conditions, using inductively coupled plasma mass spectrometry (ICP-MS) and transmission electron microscopy (TEM). Furthermore, density functional theory-based calculations and extended X-ray absorption fine structure (EXAFS) spectroscopy confirmed the formation of Th complex by these agents. Amongst the chosen biocompatible agents, tiron, SLB, PA and L52 hold promise to enhance Th decorporation for human application.
Asunto(s)
Materiales Biocompatibles/metabolismo , Torio/metabolismo , Quelantes/metabolismo , Humanos , Hígado/metabolismo , Torio/sangreRESUMEN
Ecological consequences of low-dose radioactivity from natural sources or radioactive waste are important to understand but knowledge gaps still remain. In particular, the soil transfer and bioaccumulation of radionuclides into plant roots is poorly studied. Furthermore, better knowledge of arbuscular mycorrhizal (AM) fungi association may help understand the complexities of radionuclide bioaccumulation within the rhizosphere. Plant bioaccumulation of uranium, thorium and radium was demonstrated at two field sites, where plant tissue concentrations reached up to 46.93⯵gâ¯g-1 238U, 0.67⯵gâ¯g-1 232Th and 18.27â¯kBqâ¯kg-1 226Ra. High root retention of uranium was consistent in all plant species studied. In contrast, most plants showed greater bioaccumulation of thorium and radium into above-ground tissues. The influence of specific soil parameters on root radionuclide bioaccumulation was examined. Total organic carbon significantly explained the variation in root uranium concentration, while other soil factors including copper concentration, magnesium concentration and pH significantly correlated with root concentrations of uranium, radium and thorium, respectively. All four orders of Glomeromycota were associated with root samples from both sites and all plant species studied showed varying association with AM fungi, ranging from zero to >60% root colonisation by fungal arbuscules. Previous laboratory studies using single plant-fungal species association had found a positive role of AM fungi in root uranium transfer, but no significant correlation between the amount of fungal infection and root uranium content in the field samples was found here. However, there was a significant negative correlation between AM fungal infection and radium accumulation. This study is the first to examine the role of AM fungi in radionuclide soil-plant transfer at a community level within the natural environment. We conclude that biotic factors alongside various abiotic factors influence the soil-plant transfer of radionuclides and future mechanistic studies are needed to explain these interactions in more detail.
Asunto(s)
Plantas/microbiología , Radio (Elemento)/metabolismo , Contaminantes Radiactivos del Suelo/metabolismo , Torio/metabolismo , Uranio/metabolismo , Micorrizas , Raíces de Plantas , Plantas/metabolismo , Monitoreo de RadiaciónRESUMEN
The use of uranium and to a minor extent plutonium as fuel for nuclear energy production or as components in military applications is under increasing public pressure. Uranium is weakly radioactive in its natural isotopy but its chemical toxicity, combined with its large scale industrial utilization, makes it a source of concern in terms of health impact for workers and possibly the general population. Plutonium is an artificial element that exhibits both chemical and radiological toxicities. So far, uranium (under its form uranyl, U(vi)) or plutonium (as Pu(iv)) decorporation or protecting strategies based on molecular design have been of limited efficiency to remove the actinide once incorporated after human exposure. In all cases, after human exposure, plutonium and uranium are retained in main target organs (liver, kidneys) as well as skeleton although they exhibit differences in their biodistribution. Polymers could represent an alternative strategy as their tropism for specific target organs has been reported. We recently reported on the complexation properties of methylcarboxylated polyethyleneimine (PEI-MC) with uranyl. In this report we extend our work to methylphosphonated polyethyleneimine (PEI-MP) and to the comparison between actinide oxidation states +IV (thorium) and +VI (uranyl). As a first step, thorium (Th(iv)) was used as a chemical surrogate of plutonium because of the difficulty in handling the latter in the laboratory. For both cations, U(vi) and Th(iv), the uptake curve of PEI-MP was recorded. The functionalized PEI-MP exhibits a maximum loading capacity comprised of between 0.56 and 0.80 mg of uranium (elemental) and 0.15-0.20 mg of thorium (elemental) per milligram of PEI-MP. Complexation sites of U(vi) and Th(iv) under model conditions close to physiological pH were then characterized with a combination of Fourier transform Infra Red (FT-IR) and Extended X-Ray Absorption Fine Structure (EXAFS). Although both cations exhibit different coordination modes, similar structural parameters with phosphonate functions were obtained. For example, the coordination sites are composed of fully monodentate phosphonate functions of the polymer chains. These physical chemical data represent a necessary basic chemistry approach before envisioning further biological evaluations of PEI-MP polymers towards U(vi) and Pu/Th(iv) contamination.
Asunto(s)
Elementos de Series Actinoides/química , Quelantes/metabolismo , Compuestos Organofosforados/química , Polietileneimina/química , Elementos de Series Actinoides/metabolismo , Quelantes/síntesis química , Quelantes/química , Humanos , Plutonio/química , Plutonio/metabolismo , Exposición a la Radiación , Espectroscopía Infrarroja por Transformada de Fourier , Torio/química , Torio/metabolismo , Uranio/química , Uranio/metabolismoRESUMEN
Preceramic human skeletal remains preserved in submerged caves near Tulum in the Mexican state of Quintana Roo, Mexico, reveal conflicting results regarding 14C dating. Here we use U-series techniques for dating a stalagmite overgrowing the pelvis of a human skeleton discovered in the submerged Chan Hol cave. The oldest closed system U/Th age comes from around 21 mm above the pelvis defining the terminus ante quem for the pelvis to 11311±370 y BP. However, the skeleton might be considerable older, probably as old as 13 ky BP as indicated by the speleothem stable isotope data. The Chan Hol individual confirms a late Pleistocene settling of Mesoamerica and represents one of the oldest human osteological remains in America.
Asunto(s)
Cuevas , Fósiles , Paleontología/métodos , Datación Radiométrica/métodos , Radioisótopos de Carbono/metabolismo , Humanos , México , Pelvis/anatomía & histología , Esqueleto/anatomía & histología , Torio/metabolismo , Factores de Tiempo , Uranio/metabolismoRESUMEN
Uranium ore waste has led to soil contamination that may affect both environmental and soil health. To analyze the risk of metal transfer, metal bioavailability must be estimated by measuring biological parameters. Kinetic studies allow taking into account the dynamic mechanisms of bioavailability, as well as the steady state concentration in organisms necessary to take into account for relevant risk assessment. In this way, this work aims to model the snail accumulation and excretion kinetics of uranium (U), cesium (Cs) and thorium (Th). Results indicate an absence of Cs and Th accumulation showing the low bioavailability of these two elements and a strong uranium accumulation in snails related to the levels of soil contamination. During the depuration phase, most of the uranium ingested was excreted by the snails. After removing the source of uranium by soil remediation, continued snails excretion of accumulated uranium would lead to the return of their initial internal concentration, thus the potential trophic transfer of this hazardous element would stop.
Asunto(s)
Cesio/metabolismo , Caracoles Helix/metabolismo , Modelos Biológicos , Contaminantes Radiactivos del Suelo/metabolismo , Torio/metabolismo , Uranio/metabolismo , Animales , Biodegradación Ambiental , Disponibilidad Biológica , Cesio/aislamiento & purificación , Francia , Contaminantes Radiactivos del Suelo/aislamiento & purificación , Torio/aislamiento & purificación , Uranio/aislamiento & purificaciónRESUMEN
The bioaccumulation of artificial Cs-137 and natural radionuclides Th-234, Ra-226, and K-40 by Basidiomycetes of several species is studied and evaluated in relation to their substratum soils. For this reason, 32 fungal samples, representing 30 species of Basidiomycetes, were collected along with their substratum soil samples, from six selected sampling areas in Greece. The fungal fruit bodies and the soil samples were properly treated and the activity concentrations of the studied radionuclides were measured by gamma spectroscopy. The measured radioactivity levels ranged as follows: Cs-137 from <0.1 to 87.2 ± 0.4 Bq kg(-1) fresh weight (F.W.), Th-234 from <0.5 ± 0.9 to 28.3 ± 25.5 Bq kg(-1) F.W., Ra-226 from <0.3 to 1.0 ± 0.5 Bq kg(-1) F.W., and K-40 from 56.4 ± 3.0 to 759.0 ± 28.3 Bq kg(-1) F.W. The analysis of the results supported that the bioaccumulation of the studied natural radionuclides and Cs-137 is dependent on the species and the functional group of the fungi. Fungi were found to accumulate Th-234 and not U-238. What is more, potential bioindicators for each radionuclide among the 32 species studied could be suggested for each habitat, based on their estimated concentration ratios (CRs). The calculation of the CRs' mean values for each radionuclide revealed a rank in decreasing order for all the species studied.
Asunto(s)
Basidiomycota/química , Radioisótopos de Cesio/análisis , Cuerpos Fructíferos de los Hongos/química , Radioisótopos de Potasio/análisis , Radio (Elemento)/análisis , Contaminantes Radiactivos del Suelo/análisis , Torio/análisis , Basidiomycota/crecimiento & desarrollo , Basidiomycota/metabolismo , Radioisótopos de Cesio/metabolismo , Cuerpos Fructíferos de los Hongos/crecimiento & desarrollo , Cuerpos Fructíferos de los Hongos/metabolismo , Grecia , Radioisótopos de Potasio/metabolismo , Monitoreo de Radiación/métodos , Radiactividad , Radio (Elemento)/metabolismo , Contaminantes Radiactivos del Suelo/metabolismo , Torio/metabolismoRESUMEN
The effects of different hydroponic conditions (such as concentration of thorium (Th), pH, carbonate, phosphate, organic acids, and cations) on thorium uptake by Brassica juncea var. foliosa were evaluated. The results showed that acidic cultivation solutions enhanced thorium accumulation in the plants. Phosphate and carbonate inhibited thorium accumulation in plants, possibly due to the formation of Th(HPO4)(2+), Th(HPO4)2, or Th(OH)3CO3 (-) with Th(4+), which was disadvantageous for thorium uptake in the plants. Organic aids (citric acid, oxalic acid, lactic acid) inhibited thorium accumulation in roots and increased thorium content in the shoots, which suggested that the thorium-organic complexes did not remain in the roots and were beneficial for thorium transfer from the roots to the shoots. Among three cations (such as calcium ion (Ca(2+)), ferrous ion (Fe(2+)), and zinc ion (Zn(2+))) in hydroponic media, Zn(2+) had no significant influence on thorium accumulation in the roots, Fe(2+) inhibited thorium accumulation in the roots, and Ca(2+) was found to facilitate thorium accumulation in the roots to a certain extent. This research will help to further understand the mechanism of thorium uptake in plants.
Asunto(s)
Planta de la Mostaza/metabolismo , Raíces de Plantas/metabolismo , Torio/metabolismo , Carbonatos/farmacología , Ácidos Carboxílicos/farmacología , Cationes/farmacología , Hidroponía , Planta de la Mostaza/efectos de los fármacos , Fosfatos/farmacología , Raíces de Plantas/efectos de los fármacos , Zinc/farmacologíaRESUMEN
Uranium and thorium isotopes were measured in cypress leaves, wheat grains and lettuce taken in the surroundings of the uranium conversion facility of Malvési (South of France). The comparison of activity levels and activity ratios (namely (238)U/(232)Th and (230)Th/(232)Th) in plants with those in aerosols taken at this site and plants taken far from it shows that aerosols emitted by the nuclear site (uranium releases in the atmosphere by stacks and (230)Th-rich particles emitted from artificial ponds collecting radioactive waste mud) accounts for the high activities recorded in the plant samples close to the site. The atmospheric deposition process onto the plants appears to be the dominant process in plant contamination. Dry deposition velocities of airborne uranium and thorium were measured as 4.6 × 10(-3) and 5.0 × 10(-3) m s(-1), respectively.
Asunto(s)
Contaminantes Radiactivos del Aire/metabolismo , Chamaecyparis/metabolismo , Exposición a Riesgos Ambientales , Lactuca/metabolismo , Torio/metabolismo , Triticum/metabolismo , Uranio/metabolismo , Contaminantes Radiactivos del Aire/análisis , Francia , Hojas de la Planta/metabolismo , Monitoreo de Radiación , Torio/análisis , Uranio/análisisRESUMEN
Soil-to-plant transfer factors (TFs) are of fundamental importance in assessing the environmental impact due to the presence of radioactivity in soil and agricultural crops. Tapioca and sweet potato, both root crops, are popular foodstuffs for a significant fraction of the Malaysian population, and result in intake of radionuclides. For the natural field conditions experienced in production of these foodstuffs, TFs and the annual effective dose were evaluated for the natural radionuclides (226)Ra, (232)Th, (40)K, and for the anthropogenic radionuclide (88)Y, the latter being a component of fallout. An experimental tapioca field was developed for study of the time dependence of plant uptake. For soil samples from all study locations other than the experimental field, it has been shown that these contain the artificial radionuclide (88)Y, although the uptake of (88)Y has only been observed in the roots of the plant Manihot esculenta (from which tapioca is derived) grown in mining soil. The estimated TFs for (226)Ra and (232)Th for tapioca and sweet potato are very much higher than that reported by the IAEA. For all study areas, the annual effective dose from ingestion of tapioca and sweet potato are estimated to be lower than the world average (290 µSv y(-1)).
Asunto(s)
Raíces de Plantas/metabolismo , Contaminantes Radiactivos del Suelo/metabolismo , Verduras/metabolismo , Malasia , Radioisótopos de Potasio/metabolismo , Radio (Elemento)/metabolismo , Torio/metabolismoRESUMEN
Thorium(IV) biosorption is investigated by citric acid treated mangrove endophytic fungus Fussarium sp. #ZZF51 (CA-ZZF51) from South China Sea. The biosorption process was optimized at pH 4.5, equilibrium time 90 min, initial thorium(IV) concentration 50 mg L(-1) and adsorbent dose 0.6 g L(-1) with 90.87% of removal efficiency and 75.47 mg g(-1) of adsorption capacity, which is obviously greater than that (11.35 mg g(-1)) of the untreated fungus Fussarium sp. #ZZF51 for thorium(IV) biosorption under the condition of optimization. The experimental data are analyzed by using isotherm and kinetic models. Kinetic data follow the pseudo-second-order model and equilibrium data agree very well with the Langmuir model. In addition, FTIR analysis indicates that hydroxyl, amino, and carbonyl groups act as the important roles in the adsorption process.