Search Results (177)

In situ leaching (ISL) is the most popular method for uranium mining worldwide, particularly in arid and semi-arid regions. Despite its economic benefits, ISL raises concerns about radioactive migration and groundwater contamination. This review assesses the environmental impacts of ISL uranium mining, focusing on radionuclide transport pathways and key information gaps. This review, focusing on groundwater contamination, radionuclide migration, soil and sediment contamination, atmospheric impacts, vegetation responses, and ecosystem disturbances, summarizes current understanding of the hydrogeochemical, radiological, and environmental impacts of uranium mining. The analysis indicates that groundwater is the environmental component most vulnerable to contamination during ISL operations due to the injection of acidic or alkaline leaching solutions that may mobilize uranium, radium, sulfates, selenium, arsenic, and other potentially hazardous elements. In addition to impacts on groundwater, there have also been reports of soil contamination, airborne dust, radioactive accumulation in flora, and impacts on aquatic and microbiological resources, particularly in arid and semi-arid regions. Although cleanup methods and natural attenuation can minimize contamination to some extent, residual contamination can persist for decades after mine closure. Overall, ISL uranium mining emphasizes the need for effective groundwater management, long-term environmental monitoring, and improved reclamation methods, balancing surface disturbance with long-term hydrogeochemical and environmental concerns. Full article

The Santiago River is a highly anthropogenically impaired lotic system globally, yet the mechanisms governing its contaminant transport remain poorly understood under static monitoring paradigms. This study evaluates how hydrological forcing dictates the mobilization and bioavailability of trace metals by integrating a 15-year public hydrochemical database from 10 monitoring nodes with SAR-derived discharge estimates and thermodynamic metal modeling (PHREEQC). To validate the structural integrity of the mass load estimates against hydrometric uncertainties, a deterministic boundary-sensitivity analysis was conducted. Results empirically refute the classical dilution paradigm, introducing the “Anthropogenic Pulse” to describe the non-linear acceleration of pollutant export during high-flow events (discharge Q surging from 36.62 to 286.13 m³/s). While climate-driven parameters follow seasonal cycles, industrial stressors (COD, Pb, Cd) remain in a chronic steady state, decoupling from volumetric dilution. Based on coupled × CQ × C (discharge × concentration) estimates, this dynamic induces a synchronized flushing of toxic burdens, exporting monthly peak loads exceeding 51,000 kg of Zinc, 6500 kg of Lead, and 3100 kg of Cadmium. Thermodynamic simulations reveal that this hydrological flushing functions as a chemical activator; the seasonal dilution of natural Alkalinity and Hardness suppresses the river’s theoretical buffered pH (from 8.5 to 7.0), maintaining metals in their uncomplexed free-ion states (Me²⁺). Modeling indicates that nearly 90% of the exported Cadmium remains in this highly labile, toxic form due to a dual coupling with both river Discharge (r_s = 0.87) and pH (r_s = 0.79). The identification of stochastic arsenic peaks 100 times above regulatory limits at Paso de Guadalupe (RS-08) underscores the failure of concentration-based monitoring. Our findings suggest that restoration strategies should shift toward mass-loading-based regulatory frameworks and targeted sediment management at critical nodes to mitigate the chronic export of bioavailable industrial waste. Full article

Liver fibrosis is a reversible phase of arsenic-induced chronic liver injury, with bile acid metabolic alterations closely associated with this pathological process. SIRT1 is a key metabolic regulator and promising therapeutic candidate, while its role in bile acid metabolism during arsenic-induced liver fibrosis remains poorly defined. This study established time-dependent rat models of arsenic-induced liver fibrosis with resveratrol intervention to investigate the potential association between SIRT1, bile acid metabolic disturbance, and liver fibrosis, as well as resveratrol’s hepatoprotective effects. Arsenic exposure induces progressive accumulation of hydrophobic bile acids in the liver, inflammation, hepatic stellate cell activation, and fibrosis, accompanied by suppressed expression of bile acid phase II detoxification genes (Baat, Ugt1a1, Sult2a1) and the bile acid efflux transporter gene Abcb11 (BSEP). Arsenic exposure reduces SIRT1 expression and increases C/EBPα acetylation, which may relate to impaired transcription of the aforementioned bile acid metabolic genes. Resveratrol may restore SIRT1 expression, normalize C/EBPα acetylation and bile acid homeostasis, and reduce hepatic arsenic accumulation, thereby alleviating liver fibrosis. Collectively, the SIRT1/C/EBPα axis and bile acid metabolism may be linked to the progression of arsenic-induced liver fibrosis. Resveratrol may exert protective effects via multiple mechanisms, including regulating these molecular targets and reducing hepatic arsenic accumulation. Full article

In situ leaching is increasingly used for rare earth element (REE) extraction because of its operational efficiency; however, acidic and chemically reactive leaching solutions may generate substantial environmental risks in riverine systems. This study evaluated water contamination and screening-level ecological risk following a cyanide leakage incident associated with a pilot REE mining operation in Houaphanh Province, northern Lao PDR. Surface water samples were collected from 12 downstream monitoring locations between February and April 2024. Physicochemical parameters, free cyanide (CN⁻), and dissolved metals, including arsenic (As), lead (Pb), copper (Cu), manganese (Mn), aluminum (Al), zinc (Zn), and iron (Fe), were analyzed using portable multiparameter probes, colorimetric cyanide determination, and ICP-OES. Contamination severity was interpreted using Pollution Index (PI) and Hazard Quotient (HQ) indicators based on Lao national standards and international guideline values. Results showed severe downstream contamination, with free cyanide and several dissolved metals substantially exceeding permissible thresholds. Observed elevated concentrations of As (30.29 mg/L), Pb (10.38 mg/L), Cu (14.97 mg/L), and CN⁻ (0.51 mg/L) indicated elevated ecological risk conditions, while acidic pH conditions may have enhanced metal mobilization and downstream transport. Descriptive spatial observations indicated apparent downstream contaminant dispersion within affected downstream river communities reliant on river water for domestic use, irrigation, and fisheries. Field observations additionally documented fish mortality, reduced irrigation usability, and deterioration of river water quality conditions in affected downstream communities. The findings suggest the potential vulnerability of Mekong-connected river systems to chemically intensive REE extraction activities and highlight the importance of preventive environmental governance, continuous monitoring, and operational risk management in emerging rare earth mining regions. Full article

Background: The regulation of inorganic phosphate (Pi) homeostasis is predominantly mediated by the Pi transporters belonging to the SLC34 and SLC20 families of solute carriers. However, not all Pi handling can be explained by these transporters. In this study, we sought to identify novel Pi transporters in accordance with prior findings on inhibition patterns. Methods: We have performed a functional screening of new Pi carriers using the Xenopus laevis oocyte expression system, focusing on the SLC26 family, and corroboration in cell culture. Results: Both SLC26A7 and SLC26A9 have been shown to express sodium-activated Pi uptakes with approximately 200 µmol/L Pi affinity. In both cases, Pi transport is inhibited by increasing pH and by phosphonoformate, arsenate, bicarbonate, sulfate, the chloride channel inhibitor 5-nitro-2-[(3-phenylpropyl)amino]-benzoate, and several transport site and translocation inhibitors of bicarbonate exchangers. In addition, the CFTR inhibitor GlyH-101 and the SLC4 inhibitors DIDS, SITS, and phloretin exhibited partial inhibition of SLC26A9-mediated Pi uptake. The endogenous expressions of both SLC26A7 and SLC26A9 in the renal cell lines LLC-PK1 and MDCK were primarily intracellular, colocalizing with endosomes, lysosomes, and the trans-Golgi network markers. Conversely, plasma membrane expression was found to be minimal. Pi transport in MDCK cells was sodium-independent, but when either SLC26A7 or SLC26A9 was overexpressed, sodium-activated Pi uptake was observed, along with increased expressions of SLC26A7 or SLC26A9 in the plasma membrane. Conclusions: Sodium-activated Pi transport is a novel function of the SLC26A7 and SLC26A9 multifunctional anion transporters. Further research is necessary to ascertain the relevance to Pi homeostasis in vivo. Full article

Atmospheric arsenic (As) poses significant health threats in heavily polluted urban environments. However, the size-resolved distribution of water-soluble arsenic (WSAs) in atmospheric particulate matter, as well as the size-dependent variation in As concentration and solubility under contrasting haze and non-haze conditions, remains insufficiently characterized. This study investigated the concentration, size distribution, water solubility, sources, and health risks of particulate-bound As and WSAs in Beijing from April 2014 to February 2015. The annual mean PM_0.1–18 concentration was 136.96 ± 54.21 μg·m⁻³, with significantly higher levels observed during haze episodes (179.61 ± 41.71 μg·m⁻³) compared to non-haze periods (118.00 ± 49.42 μg·m⁻³). The annual mean concentration of As was 6.42 ± 3.69 ng·m⁻³, exceeding both WHO guidelines and Chinese standards during haze periods, while WSAs averaged 4.54 ± 2.50 ng·m⁻³. Distinct size distribution patterns were observed: As displayed, a unimodal fine-mode peak (0.32–0.56 μm) was observed during haze periods and a bimodal distribution during non-haze conditions, whereas WSAs followed comparable size-dependent behavior, reflecting shifts in dominant emission sources and atmospheric processes. The average WSAs/As ratio (0.72 ± 0.07) indicated high As solubility and strong associations with secondary species and anthropogenic emissions. Size-resolved analysis revealed that As was preferentially enriched in fine particles, particularly during haze episodes, whereas coarse particles became more prominent under non-haze conditions, especially in spring, likely driven by regional dust transport and its interactions with anthropogenic emissions. Deposition modeling based on the ICRP framework showed that As and WSAs were primarily deposited in the headway (HA: 0.68 and 0.32 ng·h⁻¹, respectively), followed by the alveolar region (AR: 0.29 and 0.20 ng·h⁻¹, respectively). Fine particles enhanced deposition in deeper lung regions during haze episodes, whereas coarse particles contributed more to upper airway deposition under non-haze conditions. Although inhalation carcinogenic risks remained within acceptable limits (10⁻⁶–10⁻⁴), risks were 1.60 times higher during haze periods, with adults bearing the greatest exposure burden. These findings demonstrate that haze conditions substantially alter the size distribution, solubility, and health risks of atmospheric arsenic, and provide a scientific basis for developing size-resolved and haze-targeted heavy metal monitoring strategies in urban environments subject to significant anthropogenic pollution. Full article

Phosphogypsum (PG) stockpiles pose a persistent threat to regional water environments, yet their differential impacts on surface water and groundwater remain unclear. This study examined the pollution characteristics, sources, mechanisms, and model-predicted trends of PG-derived contaminants in both systems within a representative PG-affected region. Results showed that total phosphorus declined sharply from surface water to groundwater due to soil retention, whereas SO₄²⁻ and F⁻ remained comparable. Nitrogen species accumulated more in groundwater, indicating distinct transport and transformation processes. Arsenic was higher in surface water but rarely exceeded limits. In contrast, lead and manganese were significantly enriched in groundwater, exceeding standards by up to 27- and 11-fold, mainly due to reductive mobilization and subsurface geochemical processes. The Nemerow Index indicated heavy pollution in 35% of surface water and 43% of groundwater samples. Principal component analysis identified PG leachate as the dominant pollution source. Model predictions further suggested that increasing stockpile capacity would intensify contamination and pose long-term environmental risks. This study provided a scientific basis for understanding the distinct pollution mechanisms of PG stockpiles and offered guidance for targeted water environment management in PG-impacted areas. These findings have broader implications for regions globally facing similar challenges from industrial solid waste storage. Full article

Arsenic-contaminated groundwater is a major environmental concern, particularly in northern Argentina. Here, Microbacterium oxydans AE038-20, isolated from arsenic-rich groundwater, was investigated to elucidate its tolerance and transformation capacity. Growth assays showed that the strain tolerates inorganic arsenic [As(III), As(V)] and methylarsenite [MAs(III)] without significant inhibition. Speciation analyses revealed progressive oxidation of As(III) to As(V), reaching near-complete conversion after 10 days. Similarly, MAs(III) was fully oxidized to MAs(V). Genome sequencing identified ars-related determinants, including arsR, arsC, putative arsenite efflux systems, and arsP, supporting detoxification via arsenate reduction and arsenite efflux. Proteomic analyses confirmed the expression of proteins related to arsenic resistance, oxidative stress response, and metal transport. However, no canonical arsenite oxidases were detected at either the genomic or proteomic level. Despite this, M. oxydans AE038-20 exhibited clear arsenic oxidation activity. The detection of pigment-associated proteins and in vitro oxidation assays suggest an alternative mechanism potentially mediated by redox-active pigments. These findings highlight an alternative pathway for arsenic transformation in environmental bacteria. Full article

Arsenic contamination in polymetallic mining areas is closely linked to surrounding iron-rich manganese minerals. However, conclusive evidence remains limited regarding the retention and migration process of As(V) in naturally manganese-rich manganese ores (especially those with different manganese/iron mass ratios) under dynamic flow conditions. This study investigated As(V) adsorption and transport by four natural manganese minerals (FM1–FM4) through batch/column experiments, characterization, and numerical modeling. Their Mn/Fe mass ratios were 22.7 for FM1, 4.2 for FM2, 3.7 for FM3, and 16.4 for FM4. Batch experiments showed that As(V) adsorption on FM1–FM3 was better described by the Freundlich model, indicating heterogeneous adsorption behavior. Under the tested experimental conditions, the apparent Langmuir q_m values of these minerals decreased from 0.066 to 0.015 mmol·g⁻¹ with decreasing Mn/Fe ratio. However, As(V) adsorption on FM4, which had the lowest Mn and Fe contents, followed the Langmuir model (q_m = 0.012 mmol·g⁻¹), suggesting monolayer adsorption. Column experiments demonstrated rapid As(V) retention for all minerals. In the time domain, increasing the flow rate from 0.5 to 2.0 mL·min⁻¹ generally advanced breakthrough and shortened the desorption tail, although the breakthrough behavior expressed in pore-volume coordinates was not strictly monotonic for all minerals. The Two-Site Kinetic Attachment Model (TSKAM) successfully simulated these dynamics (R² > 0.90, RMSE < 0.05), revealing adsorption controlled by fast and slow kinetic sites, with slow-site contributions diminishing at higher flow rates. Characterization results indicated that adsorbed arsenic on FM1 remained mainly as As(V) and was immobilized primarily through surface complexation involving surface hydroxyl and Fe/Mn–O groups. XRD and SEM-EDS suggested the participation of Fe/Mn-bearing phases, while XPS on FM1 showed pronounced changes in Mn surface species during adsorption. Therefore, As(V) removal by these natural manganese minerals is a coupled physicochemical process influenced by both mineral properties, including Mn/Fe ratio, specific surface area, pore structure, pH_PZC, and Mn surface-state changes, and hydrodynamic conditions in the polymetallic mining areas. Full article

Arsenic contamination, mainly in the arsenate (As(V)) form, continues to pose a serious threat to groundwater quality worldwide due to its long-term stability and toxicity at very low levels. Herein, we demonstrate, for the first time, a three-dimensional graphene oxide-based nanocomposite composed of Cu nanoparticle-doped, amino-functionalized UiO-66 (Cu/UiO-66-NH₂) anchored on a graphene oxide framework (Cu/UiO-66-NH₂@GO) as a novel and efficient nanosorbent for the rapid removal of As(V) in groundwater-like solutions. The nanocomposite was characterized by SEM and HRTEM to confirm the hybrid structure and by XRD, N₂ adsorption–desorption isotherms, and XPS to investigate crystallinity, porosity, and surface chemistry. The derived material exhibited a highly dispersed morphology and performed rapid arsenate solid-phase extraction to attain equilibration within 10 min and was effective for a wide pH range of 2–11. The best fit for the kinetic profiles was provided by the pseudo-second-order model. Interestingly, the maximum adsorption capacity of 747.9 mg g⁻¹ at pH 6.8 was achieved, demonstrating the benefits of the complementary pairing of dispersive GO sheets and Zr-MOF adsorption domains with Cu-derived active sites. Mechanistically, the enhanced uptake is ascribed to a combination of effects, including electrostatic pre-concentration, ligand exchange, and inner-sphere complexation at metal-oxo nodes; spectroscopic analysis (XPS and FTIR) suggests that the majority of arsenate is immobilized via a strong Zr-O-As bond at coordinatively unsaturated Zr centers, which is in line with t-ZrO₂-like surface domains formed within the nanocomposite. The embedded GO support inhibits further framework interpenetration and enhances active site availability and mass transport, leading to fast and high-capacity arsenate capture in groundwater samples with related conditions. Taken together, this work presents a powerful design concept that integrates unique GO-supported, Cu-modified UiO-66-NH₂ with Zr-O binding motifs to afford high-rate remediation nanocomposites, providing an excellent platform for next-generation arsenate remediation materials. Full article

This work explores, for the first time, a novel strategy for the preparation of polymer inclusion membranes (PIMs) based on their deposition onto porous supporting substrates, introducing the concept of supported PIMs as a reagent-efficient alternative to conventional free-standing membranes. The approach aims to improve the sustainability of PIM fabrication by significantly reducing the amount of polymer and extractant required while preserving membrane functionality. PIMs were prepared using the two most widely employed base polymers, cellulose triacetate (CTA) and poly(vinyl chloride) (PVC), with Aliquat 336 as extractant. The total reagent consumption was reduced to half of the conventional formulation for CTA-based membranes and to one quarter for PVC-based membranes. Two porous supports with contrasting physicochemical properties—a hydrophilic cellulose filter paper and a hydrophobic Durapore^® PVDF membrane—were investigated. The supported membranes were characterized by contact angle measurements, SEM, FTIR, and TGA, confirming the successful integration of the PIM phase onto the porous supports without chemical alteration. Arsenate (As(V)) transport, preconcentration, and membrane reusability were evaluated. CTA-based supported PIMs exhibited transport efficiencies of approximately 90–95%, comparable to free-standing PIMs, whereas PVC-based systems showed a stronger dependence on membrane loading. Notably, CTA-based Durapore^®–PIMs retained around 70% transport efficiency after three reuse cycles. These results demonstrate the feasibility of supported PIMs as a strategy for reducing membrane material consumption while preserving functional performance. Full article

Irrigation with pig slurry has been employed to discharge large volumes of slurry and to recover resources. However, using swine wastewater for agricultural irrigation may cause the accumulation of heavy metals in soil and their potential leaching to groundwater. Wastewater treatment plants (WWTPs) are crucial to mitigate heavy metal contents in swine wastewater through physical, chemical, and biological processes. This study tracked the fate of eight heavy metals in industrial swine farms: arsenic (As), cadmium (Cd), copper (Cu), chromium (Cr), lead (Pb), mercury (Hg), nickel (Ni), and zinc (Zn). Zn reported the highest removal (82 to 99%) in all WWTPs and Cu the lowest (−5 to 97%). Cu (0.59–1.64 mg L⁻¹) and Zn (0.35–1.14 mg L⁻¹) were the metals reported in all samples for the target treatment stages (influent, after biodigester, and effluent). Comparing the heavy metal concentration in the effluents, Cu and Zn reached the highest concentrations in all WWTPs. As, Cd, and Pb reported values under the practical quantification limit. In groundwater, Cr reported the highest average concentration in farm GP19 for upstream (0.006 mg L⁻¹) and for downstream (0.032 mg L⁻¹) in GP1. In irrigated soil the Cu and Zn reported the highest concentrations in all farms, showing an enrichment compared to natural soil, indicating that wastewater is the main source of these metals in soil in the farm areas. Although all metals met the Mexican and international regulations, total suspended solids (TSSs) and chemical oxygen demand (COD) for effluent were above the reference limits (TSS ≤ 24 mg L⁻¹ and COD ≤ 72 mg L⁻¹) more than ten and four times, respectively, for all WWTPs evaluated. These two parameters were positively related and significantly correlated (p < 0.05) with the presence of metals in the different water fractions, implying possible transport of metals in solids. Cd, Pb, and As, were never reported in treated wastewater and groundwater, but Cr and Hg were. This may be related to external activities such as agriculture for Cr. The enrichment of metals in irrigated soils can be related to the metal presence in groundwater due to leaching because of the karstic soil in the area. Full article

To ensure farmland soil quality and enable the systematic management of heavy metal contamination, this study assessed cadmium (Cd), mercury (Hg), and arsenic (As) levels in 114 surface soils from farmlands across four cities in Heilongjiang Province, China. The heavy metal elements were determined and comprehensively evaluated using four indices (geo-accumulation index, single factor contamination index, Nemerow index, and potential ecological risk index). Monitoring results showed that most soil samples exhibited concentrations of Cd, Hg and As that were below the risk screening values specified in relevant standards, except for those with slightly higher Cd concentration in a few soil samples from Suihua City. Comprehensive evaluation indicated a slightly to moderately Cd contamination across the study area, with Suihua City demonstrating the most prominent pollution levels. Factors such as railway traffic emissions might have caused Cd contamination in the surrounding farmland soil. Health risk assessments confirmed that the study area posed no significant carcinogenic or non-carcinogenic risks to children or adults via soil exposure. These findings highlight the need for priority monitoring of heavy metal concentrations and implementation of targeted soil protection measures to ensure both human health and sustainable agricultural development. It is necessary to closely monitor various potential pollution sources during the operation of surrounding railway lines, which is to prevent the formation of Cd-contaminated areas due to the long-term effects of railway transportation. The results of this study will have certain significance for the evaluation and management of regional farmland land pollution. Full article

The Atacama Desert in northern Chile is characterized by its naturally high metal concentrations; however, human activities have significantly increased their availability and concentration in aquatic environments. In the Loa River basin, copper mining is the main economic activity, and the extremely arid conditions contribute to high levels of evaporation and salinity. This study evaluated the concentrations of As, Cd, and Cu in the 63 µm sediment fraction from three areas, Lequena, La Finca, and Quillagua, during the years 2014, 2015, 2017, and 2023. Contamination levels were assessed using multiple approaches, including the Geoaccumulation Index (Igeo), the Enrichment Factor (EF), the Pollution Load Index (PLI), and the mean Probable Effect Concentration Ratio (m-PEC-Q). The results showed that Lequena (upper river zone) had no evidence of anthropogenic contamination over time; however, the ecological risk assessment highlighted the significant natural contribution of arsenic, representing a potential risk to the ecosystem. In contrast, La Finca (mid-river zone) and Quillagua (river mouth) showed significantly high levels of contamination. The Geoaccumulation Index consistently classified these sites as “moderately” to “heavily” contaminated or “heavily contaminated” for arsenic, while the Enrichment Factor indicated “very high enrichment” for arsenic, reflecting a strong anthropogenic influence. Ecological risk assessments indicated a persistent 76% probability of toxicity at La Finca throughout all sampling years, a level also observed at Quillagua in 2017 and 2023, with concentrations frequently exceeding international sediment quality guidelines. These patterns are attributed to the proximity of mining activities in the middle zone and the downstream transport of contaminated sediments to the river’s mouth, resulting in persistently high ecological risks over time. This study provides important baseline information for pollution control and ecological safety in the Loa River basin. Full article

Arsenic (As) contamination in paddy soils poses a serious risk to rice safety and human health. To mitigate this issue, we developed a low-temperature, partially pyrolyzed Fe/Mn/Mg-modified biochar (FMM-BC) and evaluated its performance and mechanisms for remediating As-contaminated soil through a pakchoi–rice rotation pot experiment, aiming to reduce As accumulation in rice grains and pakchoi. The results indicated that FMM-BC application altered soil physicochemical properties and As speciation, reducing both water-soluble and bioavailable As and promoting its transformation from exchangeable to more stable organic-bound and residual fractions. Compared with the control, FMM-BC application reduced arsenic content in rice stems, leaves, and brown rice to 1.94 mg∙kg⁻¹, 5.24 mg∙kg⁻¹, and 1.21 mg∙kg⁻¹, respectively. In contrast, unmodified biochar (BC) increased As bioavailability and plant uptake, underscoring the importance of Fe/Mn/Mg modification. FMM-BC also enhanced the translocation of Fe, Mn, and Mg within rice plants, thereby modifying internal As transport dynamics and suppressing its accumulation in aboveground tissues. Under FMM-BC treatment, arsenic content in pakchoi stems and leaves decreased to 1.19 mg∙kg⁻¹ (vs. 1.96 mg∙kg⁻¹ in the control), and brown rice declined to 0.27 mg∙kg⁻¹ (vs. 1.49 mg∙kg⁻¹ in the control)—well below the national food safety threshold (0.35 mg∙kg⁻¹). These findings demonstrate that FMM-BC effectively stabilizes As in contaminated soils and reduces its transfer to edible plant parts, with Fe/Mn/Mg playing a key role in enhancing As immobilization and limiting its mobility within the soil–plant system. Full article