Stress mitigation mechanism of rice leaf microbiota amid atmospheric deposition of heavy metals.

Leaf microbiota have been extensively applied in the biological control of plant diseases, but their crucial roles in mitigating atmospheric heavy metal (HM) deposition and promoting plant growth remain poorly understood. This study demonstrates that elevated atmospheric HM deposition on rice leaves significantly shapes distinct epiphytic and endophytic microbiota across all growth stages. HM stress consistently leads to the dominance of epiphytic Pantoea and endophytic Microbacterium in rice leaves, particularly during the booting and filling stages. Leaf-bound HMs stimulate the differentiation of specialized microbial communities in both endophytic and epiphytic compartments, thereby regulating leaf microbial interactions. Metagenomic binning retrieved high-quality genomes of keystone leaf microorganisms, indicating their potential for essential metabolic functions. Notably, Pantoea and Microbacterium show significant HM resistance, plant growth-promoting capabilities, and diverse element cycling functions. They possess genes associated with metal(loid) resistance, such as ars and czc, suggesting their ability to detoxify arsenic(As) and cadmium(Cd). They also support carbon, nitrogen, and sulfur cycling, with genes linked to carbon fixation, nitrogen fixation, and sulfur reduction. Additionally, these bacteria may enhance plant stress resistance and growth by producing antioxidants, phytohormones, and other beneficial compounds, potentially improving HM stress tolerance and nutrient availability in rice plants. This study shows that atmospheric HMs affect rice leaf microbial communities, prompting plants to seek microbial help to combat stress. The unique composition and metabolic potential of rice leaf microbiota offer a novel perspective for mitigating adverse stress induced by atmospheric HM deposition. This contributes to the utilization of leaf microbiota to alleviate the negative impact of heavy metal deposition on rice development and food security.

Thallium content in vegetables and derivation of threshold for safe food production in soil: A meta-analysis.

Soil thallium (Tl) pollution is a serious environmental problem, and vegetables are the primary pathway for human exposure to Tl. Therefore, it is important to investigate the characteristics of soil Tl uptake by vegetables. In this study, the meta-analysis approach was first applied to explore the relationship between Tl content in vegetables and soil environment, as well as key factors influencing soil physical-chemical properties, and to derive soil thresholds for Tl. The results indicated that various types of vegetables have different capabilities for Tl accumulation. Vegetables from contaminated areas showed high Tl accumulation, and the geomean Tl content in different types of vegetables was in the following order: leafy > root-stalk > solanaceous vegetables. Taro and kale had significantly higher capability to accumulate soil Tl among the 35 species studied, with Tl bioconcentration factor values of 0.060 and 0.133, respectively. Pearson correlation analysis and meta-analysis revealed that the Tl content in vegetables was significantly correlated with soil pH and Tl content in soil. The linear predictive model for Tl accumulation in vegetables based on soil Tl content described the data well, and the fitting coefficient R2 increased with soil pH value. According to potential dietary toxicity, the derived soil Tl thresholds for all, leafy and root-stalk vegetables increased with an increase in soil pH, and were in the range of 1.46-6.72, 1.74-5.26 and 0.92-6.06 mg/kg, respectively. The soil Tl thresholds for kale, lettuce and carrot were in the range of 0.24-4.89, 2.94-3.32 and 3.77-14.43 mg/kg, respectively. Ingestion of kale, beet, sweet potato, potato, taro, pepper, turnip, Chinese cabbage, eggplant and carrot poses potential health risks. The study provides scientific guidance for vegetable production in Tl-contaminated areas and can help with the selection of vegetable species suitable for avoiding the absorption of Tl from contaminated soil.

Impacts of land use/cover and slope on the spatial distribution and ecological risk of trace metals in soils affected by smelting emissions.

The soil contamination around smelting sites shows high spatial heterogeneity. This study investigated the impacts of distance, land use/cover types, land slopes, wind direction, and soil properties on the distribution and ecological risk of trace metals in the soil around a copper smelter. The results demonstrated that the average concentrations of As, Cd, Cu, Pb, and Zn were 248.0, 16.8, 502.4, 885.6, and 250.2 g mg kg-1, respectively, higher than their background values. The hotspots of trace metals were primarily distributed in the soil of smelting production areas, runoff pollution areas, and areas in the dominant wind direction. The concentrations of trace metals decreased with the distance to the smelting production area. An exponential decay regression revealed that, depending on the metal species, the influence distances of smelting emissions on trace metals in soil ranged from 450 to 1000 m. Land use/cover types and land slopes significantly affected trace element concentrations in the soil around the smelter. High concentrations of trace metals were observed in farmland, grassland, and flatland areas. The average concentrations of trace metals in the soil decreased in the order of flat land > gentle slope > steep slope. Soil pH values were significantly positively correlated with Cd, Cu, Pb, Zn, and As, and SOM was significantly positively correlated with Cd, Pb, and Zn in the soil. Trace metals in the soil of the study area posed a significant ecological risk. The primary factors influencing the distribution of ecological risk, as determined by the Ctree analysis, were land slope, soil pH, and distance to the source. These results can support the rapid identification of high-risk sites and facilitate risk prevention and control around smelting sites.

[Vertical Migration Characteristics and Fate of Heavy Metals from Zinc Smelting Slag in Soil Profile].

To investigate the influence of heavy metals in smelting waste residue on the quality of soil and groundwater, a simulation column experiment was conducted to study the migration characteristics of heavy metals from the leaching solution of zinc volatilizing kiln residue in the site soil profile under continuous or intermittent leaching for 90 days. The concentrations of Cd, Cu, Pb, and Zn in leachate and their accumulation, chemical fractions, and particle size distribution characteristics in the soil profile were analyzed, and the retention mechanism of heavy metals was also discussed. The results showed that the concentration of heavy metals in the soil column leachate decreased rapidly after reaching the peak at the earlier leaching stage, and the Cd concentration far exceeded the threshold limit of 0.1 mg·L-1(class Ⅳ) of the Quality Standard for Groundwater(GB/T 14848-2017), indicating that there was Cd pollution risk of groundwater. The soil profile had a great adsorption capacity for heavy metals in the waste residue. Cd, Cu, Pb, and Zn were predominately accumulated in the shallow soil depth(0-10 cm), which was 237-429, 1.25-16.2, 1.38-2.31, and 1.79-3.17 times of the content of corresponding heavy metals in the soil profile before leaching, respectively. The migration distance of heavy metals in the slag under continuous leaching was longer than that under intermittent leaching, and Cd was significantly accumulated in the deep layer of the soil column. The contribution of soil coarse particles(0.5-2.0 mm) to the total cumulative amount of Cd, Cu, and Zn was larger, whereas Pb was more prone to accumulate in the particle size of<0.25 mm. The results of BCR sequential extraction fraction showed that the accumulated Cd, Cu, and Zn in shallow soil depth were mainly present in the weak acid extraction, accounting for 62.4%-76.7%, 72.0%-95.8%, and 67.6%-85.8% of total content, respectively. The X-ray diffraction(XRD) and Fourier transform infrared spectroscopy(FTIR) analysis showed that exogenous heavy metals in slag entering the soil would not form a stable mineral phase within 90 days, and the soil hydroxyl(-OH) and carbonyl(C=O) functional groups and iron aluminum silicate oxides were the main retention factors.

Effects of Simulated Reclaimed Water on Soil Particle Sizes and Cd Adsorption and Migration in Soils at Smelting Sites.

This work studied the vertical migration characteristics of Cd in soil profiles from a zinc smelting site under the influence of simulated reclaimed water containing NaCl and Na2SO4. The isothermal adsorption curves of Cd in the soils of miscellaneous fill and weathered slate well fitted the Freundlich and Langmuir models, with R2 ranging from 0.991 to 0.998. The maximum adsorption capacity of Cd in the soils decreased significantly under the salt ion treatments with NaCl and Na2SO4. After leaching, the Cd concentrations in the leachates and Cd contents in the subsoil layers of 10-60 cm followed the order NaCl treatment > Na2SO4 treatment > CK (p < 0.05), suggesting that the salt ions promoted the vertical migration of exogenous Cd. The proportion of coarse particles (> 0.02 mm) decreased, while that of fine particles (< 0.02 mm) increased under salt ion treatments (p < 0.05). The morphological characterization indicated that salt ions accelerated the erosion and fragmentation of coarse particles to form fine particles. The use of reclaimed water to flush smelting sites may increase the risk of Cd migration with small-sized soil particles from the soil to groundwater.

Model development and probabilistic risks of cadmium transport in slag-soil-groundwater systems with heterogeneous conditions.

Prediction of the long-term risk of trace metals leaching from soils at smelting sites is essential for groundwater protection. Herein, a mass balance-based stochastic model was developed to simulate the transport and probabilistic risks of trace metals in heterogeneous slag-soil-groundwater systems. The model was applied to a smelting slag yard with three stacking scenarios, including (A) fixed stacking amount, (B) stacking amount increasing yearly, and (C) slag removal after 20 years. The simulations suggested that the leaching flux and net accumulation of Cd in soils of the slag yard and abandoned farmland were greatest for scenario (B), which was followed by scenarios (A) and (C). In the slag yard, a plateau occurred in the Cd leaching flux curves, followed by a sharp increase. After 100 years of leaching, only scenario (B) had a high probabilistic risk (>99.9 %) of threatening groundwater safety under heterogeneous conditions. <11.1 % of the exogenous Cd may leach into groundwater under the worst scenario. The key parameters affecting Cd leaching risk include runoff interception rate (IRCR), input flux from slag release (I), and stacking time (ST). The simulation results were consistent with the values measured in a field investigation and laboratory leaching experiments. The results should help guide remediation objectives and measures to minimize the leaching risk at smelting sites.

Spatial variability of arsenic fractionation in an abandoned arsenic-containing mine: Insights into soil particle sizes and quantitative mineralogical analysis.

Soil particle sizes and mineral phases play a major role in the migration of arsenic (As) in mine. In this study, soil As fractionation and mineralogical composition in different particle sizes soil at naturally mineralized and anthropogenically disturbed zones from an abandoned mine were comprehensively studied. The results showed that soil As contents in anthropogenically disturbed mining zone (MZ), processing zone (PZ), and smelting zone (SZ) were increased with decreasing of soil particle sizes. The contents of As in the fine soil particles (0.45-2 µm) reached to 850-4800 mg·kg-1, which mainly existed at readily soluble, specifically sorbed, and Al-oxide fractions, and contributed to 25.9-62.6 % of the total As contents in soil. Conversely, soil As contents in naturally mineralized zone (NZ) were decreased with decreasing of soil particle sizes and As was mainly accumulated in the coarse fraction of soil (0.075-2 mm). Despite the speciation of As in 0.075-2 mm soil mainly existed as residual fraction, the content of non-residual As fraction reached up to 1636 mg·kg-1, indicating a high potential risk of As in naturally mineralized soil. The utilization of scanning electron microscopy, fourier transform infrared spectroscopy combined with mineral liberation analyzer revealed that soil As in NZ and PZ was mainly retained by iron (hydrogen)oxide, while whereas the dominant host minerals for soil As in MZ and SZ were the surrounding rocks of calcite and the iron-rich silicate mineral biotite. Notably, both of the calcite and biotite exhibited high mineral liberation, which was partly contributed to a significant portion of mobile As fraction in MZ and SZ soil. The results suggested that the potential risks of soil As from SZ and MZ at abandoned mine, particularly in the fine soil particles, should be a prior concern.

[Solid-solution Partitioning Coefficients and Environmental Risk of Cd and Pb in Soil in Chang-Zhu-Tan Area].

The leaching risk of heavy metals in soil has a large spatial variability on a regional scale. Taking the Chang-Zhu-Tan area as the research object, this work studied the distribution and influencing factors of available contents and solid-solution partition coefficient (Kd) of Cd and Pb in soil with land uses and clarified the environmental risk of heavy metals in soil based on Kd values measured by CaCl2 (soil-to-water ratio, 1:0.5). The results showed that the contents of available Cd and Pb in soil followed the order of forest land>suburban farmland>urban green space>industrial green space. The average Kd of Cd in soil was 449.79 L·kg-1, and that of Pb was 27604.07 L·kg-1, indicating that the mobility of Cd in the soil was significantly higher than that of Pb. The Kd values of forest soil were significantly lower than that in the other land uses. The Kd values were mainly affected by soil pH and the total content of heavy metals in soil. Adopting the available content of heavy metals measured by CaCl2 (soil-to-water ratio, 1:10) as a dependent variable, the multiple regressions effectively predicted the Kd values of Cd and Pb in soil, with R2 values of 84.2% and 67.6%, respectively. The environmental risk assessment indicated that the leaching risk in 93.8%-96.1% of the sampling sites could be ignored, whereas a few sampling sites near factories with low pH may pose a risk to the groundwater environment. The mobility of heavy metals in soil and the distribution of pollution sources determined the leaching risk of heavy metals. The results provide a method and theoretical support for preventing the environmental risk of heavy metals in soil on a regional scale.

Release characteristics of heavy metals from electrolytic manganese residue under varying environmental factors.

High levels of manganese (Mn) and other heavy metals from electrolytic manganese residue (EMR) stockpiled would be released into the environment under natural conditions. A batch-leaching test was carried out to investigate the release characteristics of heavy metals from EMR with different storage times under simulated environmental conditions such as acid rain with different pH (3.0, 4.5, 5.6, and 7.0) at contact times of 1, 2, 4, 6, and 12 h; liquid to solid ratio (L/S) (5:1, 10:1, 20:1, and 30:1); and temperature (15, 25, 35, and 45 °C). The results showed that low pH (3.0 and 4.5) and high temperature (35 and 45 °C) could significantly promote heavy metal leaching from EMRs and increasing the L/S ratio above 20:1 mL/g significantly decreased heavy metal leachate concentrations due to dilution effect. Cr, Mn, and Pb concentrations in leachate increased almost continuously throughout the leaching process, while Zn decreased slightly at the 12th hour. Meanwhile, heavy metal concentrations in EMR1 (fresh EMR) were higher than in EMR2 (out stockpiled for more than 3 months). The concentrations of Mn, Pb, and Zn in leachates from EMRs at pH 3.0 and 4.5 leaching far exceeded the allowable maximum discharge concentrations for pollutants of the integrated wastewater discharge standard in China (GB8978-1996) by 57.5-59.0, 1.3-4.3, and 1.1-1.8 and 53.5-56.0, 3.04-7.25, and 1.0-1.91 times, respectively. Additionally, the Mn concentrations from both EMR leachates at pH 7.0 were above the national safe emission threshold. The morphological structure of EMRs changed after leaching, and XRD analysis showed the disappearance of MnO2, SiO2, FeS2, and CaSO4. The XPS revealed that Cr, Mn, Pb, and Zn existed as Cr3+, MnO, PbSO4, and ZnSiO3, respectively, after leaching. The study concluded that Mn, Pb, and Zn from EMRS leached by acid rain might pose a high potential environmental risk. Therefore, developing appropriate disposal techniques for EMR is necessary to prevent heavy metal pollution.

[Component Properties and Heavy Metal Accumulation Characteristics of Contaminated Rice Straw Biochar During Oxygen-controlled Pyrolysis].

Pyrolysis is an important technology to achieve the harmlessness and recycling of contaminated biomass. In this study, the effects of oxygen-controlled atmosphere on the component properties and heavy metal accumulation characteristics of contaminated rice straw biochar were studied. The results showed that low-oxygen pyrolysis could effectively produce biochar using contaminated rice straw and improve the stability of heavy metals in biochar. Under the nitrogen atmosphere, the yield of rice straw biochar was 29.4%-34.9%. The aromatization index (SUVA254) of dissolved organic matter (DOM) increased first and then decreased with the increase in pyrolysis temperature, whereas the fluorescent components were mainly humic-like acid substances. Meanwhile, Ca mainly existed in the form of CaCO3 in biochar. Compared with the pure nitrogen condition, the biochar yield was reduced by 5.6%-13.5% and 14.9%-15.7% under the pyrolysis atmosphere containing 10% and 20% oxygen content, respectively. Ca existed in the form of CaO in biochar, which increased the pH value of the biochar by more than 0.5 units. The oxygen of the pyrolysis atmosphere accelerated the degradation of the lignin component, resulting in the gradual decrease in SUVA254 of DOM. With the increase in oxygen content in the pyrolysis atmosphere, humic-like acid substances in DOM were transformed into fulvic-like acid substances. Under the conditions of 400℃ and a 10% oxygen-containing atmosphere, the exchangeable fractions of Cu, Cd, Pb, Ni, and As in biochar were decreased by 5.2%, 3.7%, 1.7%, 0.8%, and 0.7%, respectively, indicating that heavy metals are transformed into more stable states. The results suggested that the higher biochar yield and heavy metal stability could be obtained by introducing a proper amount of nitrogen into the air (controlling the oxygen content of approximately 10%) for pyrolysis treatment of contaminated rice straw, providing an economic and feasible technology for the achievement of harmlessness and recovery of contaminated rice straw.

Impact of Vanadium-Containing Stone Coal Smelting on Trace Metals in an Agricultural Soil-Vegetable System: Accumulation, Transfer, and Health Risks.

Dietary exposure to trace metals (TMs) through vegetable consumption has been identified as a potential risk to human health. Fifty-one paired agricultural soil and leaf vegetable samples were collected around V-containing stone coal smelting sites in Hunan Province, China, to study the contamination and transfer characteristics of TMs (Cd, Cr, Cu, Pb, V, and Zn) in the soil-vegetable system. The health risk to local residents through vegetable ingestion was evaluated using Monte Carlo simulations. The results showed that 96.2%, 23.1%, 53.8%, 30.8%, 96.2%, and 69.2% of the soil samples had Cd, Cr, Cu, Pb, V, and Zn contents exceeding their related maximum allowable values, respectively. Cadmium and V were the primary pollutants based on the Igeo values. Moreover, 46.9% and 48.4% of vegetable samples exceeded the maximum permissible levels for Cd and Pb, respectively. There was a negative correlation between the bioaccumulation factors for Cd and V of the vegetable and soil physicochemical properties, including pH, organic matter, and free Fe2O3 content. Ingestion of garland chrysanthemum and pak choi posed high health risks, and Cd, V, and Pb were the primary contributors. These findings will help design strategies to minimize contamination and human exposure to soil-vegetable systems caused by V-containing stone coal smelting.

[Characteristics and Risk Assessment of Heavy Metals in the Soil Around Copper Smelting Sites].

Copper smelting can cause heavy metal pollution in surrounding soil and threaten human health. This study examined the characteristics, distribution, and health risk of heavy metals in soil with different land uses around 40 copper smelting sites at home and abroad by collecting published literature data. The results showed that the mean values of ω(As), ω(Cd), ω(Cu), ω(Pb), and ω(Zn) in the soil around the copper smelting sites were 196, 10.5, 1948, 604, and 853 mg·kg-1, respectively. The order of Igeo was Cd(5.63)>Cu(3.88)>As(2.96)>Pb(2.30)>Zn(1.27), and the accumulation of Cd and Cu was the most serious. High Nemero index (NIPI) values were found in the soil around smelting sites with a long history of smelting, outdated process, and insufficient environmental protection measures. Significant correlations were found between the concentrations of heavy metals in the soil, which decreased with the sampling distance. The heavy metals mainly accumulated within 2-3 km from the smelting sites. Compared with the smelting history, scale, and process, land use type had a lower effect on soil heavy metal concentrations. The heavy metals in the soil around copper smelters may pose carcinogenic and non-carcinogenic risks on residents. The high health risks were mainly caused by As and Pb in smelting production areas, and Pb in woodland. These results may guide the risk prevention of heavy metal pollution in the soil around smelting sites.

[Potential of Intercropping Pennisetum purpureum Schum with Melia azedarach L. and Broussonetia papyrifera for Phytoremediation of Heavy-metal Contaminated Soil around Mining Areas].

In order to study the potential of intercropping Pennisetum purpureum Schum with Melia azedarach L. and Broussonetia papyrifera for phytoremediation of heavy-metal contaminated soil around mining areas, a pot experiment was conducted to investigate the effects of intercropping on plant biomass, heavy metal accumulation, dynamic changes in heavy metal content in soil solution, and response characteristics of the rhizosphere microbial community. The results indicated that the shoot biomass of P. purpureum and M. azedarach from their intercropping system (KX) was increased by 26.5% and 13.2%, respectively, and the shoot biomass of B. papyrifera from the intercropping system of P. purpureum and B. papyrifera (GX) was increased by 13.5% compared with their corresponding monoculture systems. The shoot Cd content of M. azedarach in the KX treatment was significantly increased by 24.9% (P<0.05), and their Cd and Pb accumulation in shoots were also significantly increased. The shoot contents and accumulations of Cd and Pb from P. purpureum in the GX treatment were significantly increased; however, those in B. papyrifera shoots were decreased. The total accumulations of Cd and Pb in each pot from intercropping systems were higher than that from the monoculture treatment, with that from the KX treatment being the highest at 1065 µg·pot-1. During the 150-day cultivation process, the pH value and dissolved organic carbon (DOC) content in the soil solution under the intercropping systems of KX and GX were higher than those of original soil (CK). After 150 d cultivation, the DOC contents of the soil solution under the KX and GX treatments were significantly increased by 40.5% and 33.1% in comparison with that under CK (P<0.05), respectively. Compared with those from CK and P. purpureum and B. papyrifera monoculture treatments, the Cd content in soil solution from the KX treatment was significantly decreased by 56.1%, 35.5%, and 46.5%, and that in the GX treatment was decreased by 54.5%, 33.2%, and 44.6% (P<0.05), respectively. The Shannon and Chao1 indices of rhizosphere microorganisms under the intercropping systems were significantly higher than those under CK. The number of unique OTUs in intercropping systems was significantly higher than that in CK and the M. azedarach and B. papyrifera monocultures. Intercropping improved the abundance of dominant bacteria such as Actinobacteriota and Acidobacteriota, and the abundance of Actinobacteriota increased by 31.6%, 20.9%, and 25.3% in the KX treatment and by 32.3%, 21.5%, and 25.9% in the GX treatment, respectively, in comparison with those in CK and the P. purpureum and M. azedarach monocultures. It was concluded that intercropping P. purpureum with wood plants could increase their shoot biomass and the accumulations of Cd and Pb, as well as soil environmental quality, whereas the availability and migration risk of heavy metals in soil were reduced. Moreover, the intercropping of P. purpureum and M. azedarach was more beneficial to the remediation of polymetallic-contaminated soil around mining areas.

Leaching and characterization studies of heavy metals in contaminated soil using sequenced reagents of oxalic acid, citric acid, and a copolymer of maleic and acrylic acid instead of ethylenediaminetetraacetic acid.

In this work, the removal performance of three environmentally friendly reagents, oxalic acid (OA), citric acid (CA), and a copolymer of maleic and acrylic acid (PMAA), on heavy metals in polluted soil was studied at the optimum conditions and compared their sequenced performance. The results showed that the consecutive washing with the individual acids significantly improved the removal percentage of heavy metals in the soil compared to that of EDTA (10.2%, 71.3%, 29.8%, 61.6%, and 52.4% removal for As, Cd, Cu, Pb, and Zn, respectively). The removal of As, Cd, Cu, Pb, and Zn in the sequence of CA-OA was 65.6%, 79%, 59.1%, 64.6%, and 63.5%, respectively. In addition, the organic acids had little influence on the soil physicochemical properties after washing with slight reductions of acidity (pH) and soil organic matter (SOM), which are the major determinants of the usability of washed soils for plant growth. The germination rate of Sorghum bicolor in CA-OA-washed soils reached over 70% on the 7th day. CA-OA-washed soils collectively stand out in using washed soils for plant growth with the following advantages: simultaneous removal of cationic and anionic metals, less harmful impact on soil properties, and successful support for the germination of crops. Based on the findings, we recommend the CA-OA sequence as the best alternative to EDTA with higher metal removal efficiency and germination success.

Contamination vertical distribution and key factors identification of metal(loid)s in site soil from an abandoned Pb/Zn smelter using machine learning.

Soil heterogeneity makes the vertical distribution of metal(loid)s in site soil vary considerably and poses a challenge for identifying the key factors of metal(loid)s migration in site soil profiles. In this study, a machine learning (ML) model was developed to study a typical abandoned Pb/Zn smelter using 267 site soils from 46 drilling points. Results showed that a well-trained ML model could be used to identify the key factors in determining the contamination vertical distribution and predict the metal(loid)s contents in subsurface soil. As, Cd, Pb, and Zn were the primary pollutants and their vertical migration depth arrived to 4-6 m. Based on the predictive performance of different ML algorithms, the extreme gradient boosting (XGB) was selected as the best model to produce accurate predictions for the most metal(loid)s content. Contents of As, Cd, Pb, and Zn in the heavily contaminated zones declined with an increase of soil depth. The metal(loid) contents in surface soil of 0-2 m could be readily used to predict the content of Cd, Cr, Hg, and Zn in subsurface soil from 2 m to 10 m. Based on the metal-specific XGB models, sulfur content, functional area, and soil texture were identified as key factors affecting the vertical distribution of As, Cd, Pb, and Zn in site soil. Results suggested the ML method is helpful to manage the potential environmental risks of metal(loid)s in Pb/Zn smelting site.

[Effect of Butyl Xanthate on Pb2+ and Cd2+ Adsorption by Soil Around a Dressing Plant].

Flotation agents can enter the soil and water environment around mining areas through beneficiation wastewater discharge and overflow from tailings ponds. The adsorption of Pb2+ and Cd2+ on soil around a lead-zinc dressing plant was investigated in the presence of potassium butyl xanthate (PBX). Batch experiments were conducted with different initial pH, PBX, Pb2+, and Cd2+solution concentrations. The fractions of lead and cadmium were altered after treatment with different concentrations of PBX. The results showed that adsorption of Pb2+and Cd2+ on soil was seriously inhibited by PBX. When PBX concentration was 40 mg·L-1, the adsorption capacity of Pb2+ and Cd2+ decreased from 3540 mg·kg-1 and 387 mg·kg-1 to 3085 mg·kg-1 and 100 mg·kg-1, respectively. The Pb2+ and Cd2+ adsorption kinetic process was best fitted by the quasi-second-order kinetic model, which indicated that the adsorption process of Pb2+ and Cd2+ on soil was mainly chemical adsorption. The formation of a hydrophobic and insoluble complex and competitive adsorption between PBX, Pb2+, and Cd2+ on the soil surface was the main reason for reducing the adsorption capacity. The results showed that PBX could increase the mobility of Pb2+ and Cd2+ on soil. The degree of impact improved with increasing initial concentration of PBX and pH but decreased with increasing initial concentration of Pb2+ and Cd2+, and the adsorption isotherms conformed to the Freundlich isotherm. Under low PBX content (100 mg·kg-1), exchangeable and reducible cadmium contents in the soil increased, which could lead to the activation of cadmium in soil. However, the addition of PBX to the treated soil could reduce the content of exchangeable and reducible lead. As the concentration of PBX increased, the reduction effect also increased, which was related to the stronger complex stability of Pb(C4H9OCS2)2 than that of Cd(C4H9OCS2)2. The results showed that residual flotation reagents in beneficiation wastewater may increase the potential ecological risk of heavy metals such as Pb and Cd in soil, and the prevention and control of the potential ecological risk should be strengthened.

Pollution and Risk Assessments of Heavy Metal(loid)s in the Soil around Lead-Zinc Smelteries via Data Integration Analysis.

Pb-Zn smelting is a major cause of heavy metal(loid) contaminations in soils. We collected data on heavy metal(loid)s in the soils near Pb-Zn smelteries globally from 54 peer-reviewed reports to study the metals' distribution, pollution index, and potential ecological and health risks. We observed that 90% of the studied Pb-Zn smelteries were distributed in Asia and Europe. Heavy metal(loid)s were mainly deposited within a 2 km distance to the smelteries, with mean concentrations (mg/kg) of 208.3 for As, 26.6 for Cd, 191.8 for Cu, 4192.6 for Pb, and 4187.7 for Zn, respectively. Cd and Pb concentrations in the soil exceeded their corresponding upper continental crust values several hundred folds, suggesting severe contamination. The smelting area had the highest heavy metal(loid) contamination in soil, followed by the forest land, farmland, and living area. Compared with the soil environmental standard values from various countries, As, Cd, Pb, and Zn were considered priority pollutants for protecting the ecosystem and human health. Likewise, As, Cd, and Pb were suggested as the priority pollutants for protecting groundwater safety. The potential ecological and health risks of heavy metal(loid)s in the soil within 2 km of Pb-Zn smelteries were severe and should be of concern.

Phytoextraction potential of arsenic and cadmium and response of rhizosphere microbial community by intercropping with two types of hyperaccumulators.

Intercropping with hyperaccumulators/accumulators is a promising alternative to enhance phytoextraction of heavy metal(loid)s in contaminated soil. In this research, a pot experiment was conducted to evaluate the influences of intercropping As hyperaccumulator Pteris vittata L. with Cd hyperaccumulator Sedum alfredii Hance or accumulator Hylotelephium spectabile (Boreau) H. Ohba on the plant growth, As and Cd phytoextraction, and rhizosphere bacterial microbiota. The results indicated that intercropping can promote the growth of plants. The total biomass of P. vittata, S. alfredii, and H. spectabile in intercropping systems was improved by 19.9-34.1%, 16.8%, and 11.5%, respectively, in comparison with corresponding plant monoculture. The As content in rhizoid and frond of P. vittata when intercropped with S. alfredii was significantly increased by 28.3% and 19.0% (P < 0.05), respectively, as compared with P. vittata monoculture, and this treatment acquired the maximum As and Cd accumulation with 2032 µg·pot-1 and 397 µg·pot-1, respectively. Intercropping enhanced the soil bacterial community diversity. The genera of Lysobacter in P. vittata rhizosphere and Massilia and Arthrobacter in S. alfredii rhizosphere had higher abundance in the intercropping system of P. vittata and S. alfredii. There were significantly positive correlation relationships between Massilia and Arthrobacter with plant Cd content and Lysobacter with plant As content, indicating that they may play important roles in As and Cd phytoextraction. The results suggested that intercropping P. vittata with S. alfredii could be a potential strategy for phytoextraction of As and Cd from co-contaminated soil.

Pollution characteristics and environmental availability of toxic elements in soil from an abandoned arsenic-containing mine.

Understanding the pollution characteristics and assessing the ecological risk of toxic metals in mine soil are crucial to controlling and managing risks in abandoned mine areas. In this study, the profile soil pollution characteristics and modified ecological risk of As, Cd, Hg, Pb, Sb, and Tl for both the different mining functional areas and the downstream impacted areas at a large-scale abandoned arsenic-containing mine were studied. Results showed that both the profile soils at the mining functional areas and the surface layer in downstream sites are heavily polluted by As, Cd, Hg, Sb, and Tl. As, Hg, Sb, and Tl mainly accumulated on soils with a depth of 0-1.5 m. In contrast, these metals in the mining site were gradually increased with soil depth above the bedrock strata. Cd and Pb were mainly concentrated at depth of 2.5-3.5 m in the smelting with by-product processing site. The speciation of metals in the profile soils mainly occurred in residual fraction. However, high levels of potential mobile As and Sb were found in mining soils and smelting surface soils, as well as Tl in deep soils at mining functional sites and top soils at downstream sites, with their mean contents in these areas arrived to 2950 mg kg-1, 9.64 mg kg-1, and 0.98 mg kg-1, respectively. In addition, the modified ecological risk assessment (NIRIm) values revealed a substantial ecological risk of As, Cd, Hg, and Sb in both the entire profile soils at the mining, smelting sites and topsoil (0-1.5 m) at the adjacent downstream site. In summary, the pollution characteristics and potential ecological risk of toxic metals in profile soils from the different functional sites at arsenic-containing mine were significantly different and suitable control strategies for available toxic elements should be adopted in the different functional sites of mine.

Diorganotin(IV) complexes based on tridentate ONO ligands as potential anticancer agents.

Eight new diorganotin(IV) complexes (1a-2d), namely {[X-C6H4(O)C=N-N=C(Me)COO]R2Sn(CH3OH)}n (1a, 2a), {[X-C6H4(O)C=N-N=C(Me)COO]R2Sn(CH3OH)}2 (1b, 1c, 1d, 2b), and {[X-C6H4(O)C=N-N=C(Me)COO]R2Sn}2 (2c, 2d) (X = H-, p-Me-, p-OH-, p-NO2-; R = o-Cl-C6H4CH2- or o-Me-C6H4CH2-), have been synthesized by microwave "one-pot" reaction with arylformylhydrazine, pyruvic acid, and the corresponding R2SnCl2. All the complexes have been characterized by FT-IR (Fourier transform infrared spectroscopy), multinuclear NMR (1H, 13C, and 119Sn nuclear magnetic resonance spectroscopies), HRMS (high-resolution mass spectroscopy) and single-crystal X-ray structural analysis. The antiproliferative activity of all complexes was tested against the cancer cell lines NCI-H460, MCF-7 and HepG2. The diorganotin complex 1c has been shown to be more potent antitumor agents against HepG2 than other complexes and cisplatin. Flow cytometry analysis observation demonstrated that complex 1c mediated cell apoptosis of HepG2 cells and arrested cell cycle in the S phase. The single cell gel electrophoreses assay results show that the 1c induce DNA damage. The DNA binding activities of the 1c were studied by UV-visible absorption spectrometry, fluorescence competitive, circular dichroism measurements, and molecular docking, results shown 1c can be well embedded in the groove and cleave DNA.