Probabilistic human health risk assessment of PCDD/Fs near municipal solid-waste incinerator using Monte Carlo analysis coupled with triangular fuzzy numbers.

PCDD/Fs are dioxins produced by waste incineration and pose risks to human health. We aimed to detail the health risks of airborne and soil PCDD/Fs near a municipal solid-waste incinerator (MSWI) for the surrounding population and develop a new model that improves upon existing methods. Thus, we conducted field sampling and then investigated a MSWI in the Pearl River Delta (2016-2018). Our results showed that the carcinogenic and non-carcinogenic risk values of PCDD/Fs exposed to residents in nearby areas were acceptable, with hazard index (HI) values lower than 1.0 and a total carcinogenic risk lower than 1.0E-6. Notably, the results raised concerns regarding higher non-carcinogenic risks in children than in adults. Comparative analysis of the frequency accumulation diagram, accumulated probability risk, and the absolute value of error (δ) between the 95% confidence interval (CI) and the 90% CI of the Monte Carlo stochastic simulation-triangular fuzzy number (MCSS-TFN) and the MCSS model, respectively, demonstrated that the MCSS-TFN exhibited less uncertainty than the MCSS model, regardless of the health risk value of PCDD/Fs in ambient air or in soil. This observation underscores the superiority of the MCSS-TFN model over other models in assessing the health risks associated with PCDD/Fs in situations with limited data. Our new method overcomes the limited dataset size and high uncertainty in assessing the health risks of dioxin substances, providing a more comprehensive understanding of their associated health risks than MCSS models.

Spatiotemporal response of the optical characteristics of dissolved organic matter to seasonality and land use in tropical island rivers.

Dissolved organic matter (DOM), a pivotal component in the global carbon cycle, plays a crucial role in maintaining the productivity and functionality of aquatic ecosystems. However, the driving factors of variations in the properties of riverine DOM in tropical islands still remain unclear. In this study, the spatiotemporal response of the optical characteristics of riverine DOM to seasonality and land use on Hainan Island in southern China was investigated. Our results revealed that DOM in the rivers of Hainan Island exhibited a relatively high proportion of fulvic acid and demonstrated strong terrestrial sources. The optical properties of DOM exhibited significant variations both seasonally and spatially. Land use exerted a dominant influence on riverine DOM. Specifically, during the wet season, riverine DOM exhibited larger molecular weight, increased chromophoric DOM (CDOM) abundance, and higher Fmax compared to the dry season. Furthermore, riverine DOM influenced by grassland and farmland showed higher CDOM abundance, Fmax, and humification degree in contrast to those impacted by forest and urban. Random forest and correlation analysis results indicated that grassland and farmland enhanced the Fmax of DOM by increasing levels of TP, NO3--N, Chl a, and NH4+-N in the dry season. However, during the wet season, the increased Fmax of DOM induced by grassland and farmland relied on the increments of Chl a and TP concentrations. This study improves our understanding of the spatiotemporal fluctuations of DOM in the rivers of Hainan Island, highlighting the effects of season and land use on DOM. It offers valuable support for improving water quality and contributes to enhancing human comprehension of the global carbon cycle.

Effects of multiwalled carbon nanotubes on the dissolved organic matter released by Prorocentrum donghaiense: Results of spectroscopic studies.

Many reports have investigated the effects of carbon nanotubes (CNTs) on the properties of terrestrial dissolved organic matter (DOM), which could significantly altered its binding affinity for contaminants. However, the effects of CNTs on algogenic DOM are largely unknown. To address this issue, the properties of algogenic DOM released by Prorocentrum donghaiense (P. donghaiense-DOM) under the stress from 0.1 to 10.0 mg/L graphitized multiwalled CNTs were nondestructively characterized by the use of UV-visible absorption and fluorescence excitation-emission matrices with parallel factor analysis. The results showed that the changes in the properties of P. donghaiense-DOM were highly dependent on the CNTs concentration. The properties of P. donghaiense-DOM under 0.1 mg/L CNTs treatment showed no obvious differences compared to the control. The addition of 0.5-10.0 mg/L CNTs changed the release pathways of P. donghaiense-DOM, resulting in significant alterations to the properties of P. donghaiense-DOM. The aromaticity, molecular weight, protein-like and humic-like components were enhanced under stress from 0.5 to 1.0 mg/L CNTs on day 4, which can be ascribed to the overproduction of extracellular DOM (EDOM) that occurred in response to the significant increase in intracellular ROS levels. CNTs at 5.0 and 10.0 mg/L significantly induced membrane damage to P. donghaiense on day 4, which led to the leakage of intracellular DOM (IDOM) and then increased the molecular weight and protein-like components but decreased the aromaticity and humic-like components. After the P. donghaiense recovered to its normal growth under 0.5-10.0 mg/L CNTs treatments, the changes in the properties of P. donghaiense-DOM were attributed to the release pathways of P. donghaiense-DOM that were governed by the production of EDOM and the leakage of IDOM in the stationary and declining phases, respectively.

[The new applications of NMR technology in the field of characterization of surface properties of the material].

Nuclear magnetic resonance (NMR) technology has been developed continuely because of its rapid, accurate and high resolution advantages, The technology has become an important method to analyze the soil properties, and to identify the structure of matters, food analysis, medical imaging fields. This study summarized two aspects of the important applications of NMR in the characterization of the surface properties of materials. First, the use of NMR techniques for the adsorption, desorption and diffusion behaviors of polymer on solid particles (mainly SiO2 particles). Sencond, to investigate the wettability and water uptake progress of contaminated soils using NMR techniques. This study summarized the important applications of NMR techniques in the characterization of surface properties. It also showed the unique application in the field of polymer materials and environment. This study introduced the measured method for the relaxation time of substance using acorn surface area analyzer in the liquid environment. It reflect the surface properties and structural features of substance. It also provided data support for the explanation of environmental behaviors of contaminants and thus, it played an important role in the environmental field. Compared to the conventional BET method, acorn surface area analyzer showed the advantages in terms of conditions and time measurement. Especially, traditional BET method cannot get the information of the specific surface area of substances in the liquid directly, but acorn surface area analyzer solved the difficult problem. It is a new breakthrough in the field of characterization of the surface properties of materials by NMR in the liquid. We analyzed the application of acorn surface area analyzer in pharmaceuticals, cosmetic materials, electronic products because acorn surface area analyzer could reflects the important characteristics of the surface properties and structural features of substance. And we provide the prospective of the applications of NMR techniques in organic matter of soils, drug and natural products detecting.

Differences in the uptake and translocation of differentially charged microplastics by the taproot and lateral root of mangroves.

The interception of microplastics (MPs) by mangrove roots plays an indispensable role in reducing the environmental risks of MPs. However, there remains limited research on the fate of the intercepted MPs. Hereby, the uptake and subsequent translocation of 0.2 µm and 2 µm PS MPs with different coating charge by the typical salt-secreting mangrove plants (Aegiceras corniculatum) were investigated. Compared to amino-functionalized PS with positive charge (PS-NH2), the visualized results indicated that the efficient uptake of carboxy-functionalized PS with negative charge (PS-COOH) was more dependent on taproots. But for the lateral roots, it only allowed the entry of PS-NH2 instead of PS-COOH. The specific uptake pathways of PS-NH2 on the lateral roots could attribute to the release of H+ and organic acids by root hairs, as well as the relative higher Zeta potential. After entering the Aegiceras corniculatum roots, the translocation of PS MPs was restricted by their particle sizes. Furthermore, the release of PS MPs from Aegiceras corniculatum leaf surfaces through the salt glands and stomata was observed. And the decline in the photochemical efficiency of leaves under PS MPs exposure also indirectly proved the foliar emission of PS MPs. Our study improved the understanding of the environmental behaviors and risks of the retained MPs in mangroves.

Health assessment based on exposure to microplastics in tropical agricultural soil.

Microplastic (MP) pollution of agricultural soils has caused global alarm over its widespread distribution and potential risks to terrestrial ecosystems and human health. This study assessed human health based on exposure to soil MPs through a comprehensive investigation of the factors influencing their occurrence and spatial distribution on Hainan Island, South China. The results showed that the abundance of soil MPs was 1128.6 ± 391.5 items·kg-1, whereas the normalized abundance of MPs based on using a power-law function was 19,261.4 items·kg-1. Regarding the extent of population exposure to agricultural soil MPs, the average daily exposure dose (pADD) model revealed that using mass as an indicator to assess the health risks associated with MP intake is more reliable than using abundance. However, abundance-based exposure assessments are also relevant because MPs with smaller particle sizes are more harmful to human health. Moreover, for adults, the normalized pADD values based on abundance and mass were 1.68E-02 item MPs·kg BW-1·d-1 and 7.23E-02 mg MPs·kg BW-1·d-1, respectively. Although the multidimensionality of MPs should be further aligned and quantified, the preliminary findings of this study contribute to the development of human health risk assessment frameworks for soil MPs.

An unrecognized entry pathway of submicrometre plastics into crop root: The split of hole in protective layer.

Threats to food safety caused by the continuous accumulation of plastic particles in the terrestrial environment is currently a worldwide concern. To date, descriptions of how plastic particles pass the external biological barrier of crop root have been vague. Here, we demonstrated that submicrometre polystyrene particles passed unimpededly the external biological barrier of maize through the split of holes in the protective layer. We identified plastic particles induced the apical epidermal cells of root tips become round, thereby expanding the intercellular space. It further pulled apart the protective layer between the epidermal cells, and eventually formed the entry pathway for plastic particles. The enhancement of oxidative stress level induced by plastic particles was the main reason for the deformation of the apical epidermal cells (increased roundness values: 15.5%), comparing to the control. Our findings further indicated that the presence of cadmium was conducive to the "holes" formation. Our results highlighted the critical insights into the fracture mechanisms of plastic particles for the external biological barriers of crop roots, providing a strong incentive to access the risk of plastic particles in agriculture security.

The role of pores in micro-zone distribution of Cd in a tropical paddy soil: Results from X-ray computed tomography combined energy dispersive spectroscopy analysis.

Accurate description of Cd micro-zone distribution and accumulation is the prerequisite for revealing Cd transfer and transformation processes. However, to date, the role of soil pores in the Cd micro-zone distribution characteristics in undisturbed soil is still unclear. In this study, the obvious heterogeneous distribution of Cd in and around the soil pores at the cross-sectional surface of the tropical undisturbed topsoil was visualized by the combination of X-ray micro-computed tomography and scanning electron microscope-energy dispersive spectroscopy. For both the air space and water-holding pores, the micro-zone distribution characteristics of Cd around the pores were dominated by pore sizes. For macropores and mesopores, Cd preferred to distribute in the micro-zone within 167.5-335 µm from pores. But for micropores, the highest content percentage of Cd was exhibited in the micro-zone within 67-167.5 µm from pores. The random forest model revealed that the occurrence of Fe (13.83%) and P (13.59%) contributed most to Cd micro-zone distribution around air space pores. While for water-holding pores, Fe occurrence (18.30%) contributed more significantly than P (11.92%) to Cd micro-zone distribution. Our study provided new insights into Cd retention mechanism, which is help for accessing Cd migration and transformation.

Phosphorus fractions and iron oxides responsible for the variations in the Cd retention capacity in tropical soil aggregates under different cropping patterns.

The environmental behavior of Cd in soil has been widely studied because of its close relationship with food security and soil environmental pollution. In this study, the roles of P fractions and Fe oxides in the retention of Cd in typical tropical soil from five cropping patterns were investigated. Although there was no evident relationship between the Cd adsorption capacity and soil aggregate particle sizes, strong spatial associations of P, Fe, and Cd at the soil aggregates were observed via energy dispersive spectroscopy analysis. Among five cropping patterns, citrus plantations exhibited highest ratios (calculated by pixel area) of P overlapped with Cd (8.61%) and Fe overlapped with Cd (9.53%) in the microaggregates. Furthermore, the random forest model revealed that humic P and labile organic P greatly contributed to the sorptivity of Cd2+ by < 0.053 mm (13.3%) and 0.25-0.053 mm (13.4%) soil aggregates, respectively. Compared with the P fractions in different-sized soil aggregates, the contribution of Fe oxides to the sorption of Cd2+ by soil aggregates was more significant. Amorphous ferric oxide had the most significant contribution to the sorptivity of Cd2+ by < 0.053 mm (26.0%), 0.25-0.053 mm (23.0%), 2.0-0.25 mm (25.1%), and > 2.0 mm (33.9%) soil aggregates.

Health risk assessment of trace metal(loid)s in agricultural soil using an integrated model combining soil-related and plants-accumulation exposures: A case study on Hainan Island, South China.

Traditional health risk assessment of trace metal(loid)s (TMs) in agricultural soil exclusively considers direct soil-related exposure and may underestimate the health risks they pose. In this study, the health risks of TMs were evaluated using an integrated model that combined soil-related and plant-accumulating exposures. A detailed investigation of common TMs (Cr, Pb, Cd, As, and Hg) coupled with probability risk analysis based on a Monte Carlo simulation was conducted on Hainan Island. Our results showed that, except for As, the non-carcinogenic risk (HI) and carcinogenic risk (CR) of the TMs were all within the acceptable ranges (HI < 1.0, and CR < 1E-06) for direct soil-related exposure to bio-accessible fractions and indirect exposure via plant accumulation (CR substantially lower than the warning threshold 1E-04). We identified crop food ingestion as the essential pathway for TM exposure and As as the critical toxic element in terms of risk control. Moreover, we determined that RfDo and SFo are the most suitable parameters for assessing As health risk severity. Our study demonstrated that the proposed integrated model combining soil-related and plant-accumulating exposures can avoid major health risk assessment deviations. The results obtained and the integrated model proposed in this study can facilitate future multi-pathway exposure research and could be the basis for determining agricultural soil quality criteria in tropical areas.

How surfactants affect the depuration of polycyclic aromatic hydrocarbons adsorbed on the mangrove leaf surfaces: insight from an in situ method.

The effects of sodium dodecyl benzene sulfonate (SDBS), polyoxyethylene (20) sorbitan monolaurate (Tween 20), and their mixtures on the depuration of anthracene (Ant) and fluoranthene (Fla) individually adsorbed on the Kandelia obovata (Ko) leaf surfaces were in situ investigated. The Ko original leaf-wax microstructures have been destroyed by SDBS, Tween 20, and their mixtures at or above their critical micelle concentration (CMC). The volatilization rate constants (kV) of the adsorbed PAHs decreased with surfactants at or above their CMC resulting from the plasticizing effect and a decrease in the polarity of the Ko leaf-waxes induced by surfactants. Moreover, the photolysis rate constants (kP) of the adsorbed PAHs decreased with SDBS while increased with Tween 20 and their mixtures at or above their CMC, which can be attributed to effects of surfactants on the light adsorption behavior of Ko leaf-waxes. Overall, the effects of surfactants on the depuration of the adsorbed PAHs were dependent not only on the physical-chemical properties of surfactants but also on the micro-environment of the substrates adsorbed the PAHs. These results are of great significance for further understanding the accumulation of PAHs and could expand our knowledge about the migration mechanism of PAHs from the atmosphere by mangrove leaf surface micro-zones.

Mangrove leaves: An undeniably important sink of MPs from tidal water and air.

Capturing microplastics (MPs) were one of the important characteristics for terrestrial plant. Whereas, role of mangrove leaves in capturing MPs from tidal water and air were still largely unexplored. Here, we detected the spatial distribution of MPs at both submerged (0.10-0.49 n/cm2) and non-submerged mangrove leaves (0.09-0.24 n/cm2) in the Beibu Gulf. Abundance of MPs on submerged mangrove leaves was significantly higher than that on non-submerged mangrove leaves in landward and middle zone (*p < 0.05). Almost no difference existed in the abundances of MPs detected on leaves of different mangrove species. Abundance of MPs on submerged mangrove leaves increased following the sequences of seaward zone (0.11 n/cm2) < middle zone (0.21 n/cm2) < landward zone (0.36 n/cm2). PE MPs with uncoloured/fiber characteristics dominated the MPs both on the non-submerged and submerged mangrove leaves. Furthermore, contribution of tidal water was significantly greater than that of atmospheric deposition on MPs retention on submerged mangrove leaves. Results of this work highlight the importance of tidal water and air in the spatial distribution of MPs at mangrove leaves, and the globally MPs gross reserves at mangrove leaves cannot be ignored in evaluating the MPs sink in mangrove wetland.

The distribution and retained amount of benzo[a]pyrene at the micro-zones of mangrove leaf cuticles: Results from a novel analytical method.

Plant leaf cuticles play a critical role in the accumulation and transport of atmospheric polycyclic aromatic hydrocarbons (PAHs). The relationship between the distribution and retained amount of PAHs on the leaf cuticles and the leaves micro-zone structures is still unclear. In this study, a confocal microscopic fluorescence spectral analysis (CMFSA) system with a spatial resolution of 200 nm was established as a direct and noninvasive means to determine the microscopic distribution and quantify the retained amount of benzo[a]pyrene (B[a]P) at Aegiceras corniculatum (Ac), Kandelia obovata (Ko) and Avicennia marina (Am) leaf cuticle micro-zones (0.096 mm2). The linear ranges for the established method were 10-1900 ng spot-1 for Ac, 15-1700 ng spot-1 for Ko and 30-1800 ng spot-1 for Am, and the detection limits were 0.06 ng spot-1 for Ac, 0.06 ng spot-1 for Ko and 0.07 ng spot-1 for Am. Notably, B[a]P formed clusters and unevenly distributed at the leaf cuticles. On the adaxial cuticles, B[a]P was mainly accumulated unevenly along the epidermis cell wall, and it was also distinctively distributed in the secretory cells around salt glands for Ac and Am. On the abaxial leaf cuticles, B[a]P was concentrated in the salt glands and stomata apart from being unevenly distributed in the epidermis cell wall. Moreover, the amount of B[a]P retained presented a negative correlation with the polarity of leaf cuticles, which resulted in the amount of B[a]P retained on the adaxial leaf cuticles being significantly higher than that on abaxial leaf cuticles. Our results provide a potential in situ method for investigating the distribution and retained amount of PAHs at plant leaf surface micro-zones, which would contribute to further studying and understanding the mechanism of migration and transformation of PAHs by plant leaves from a microscopic perspective.

Adsorption of bisphenol A on dispersed carbon nanotubes: Role of different dispersing agents.

Although the adsorption of organic contaminants on carbon nanotubes (CNTs) and the dispersion of CNTs have been extensively investigated separately, the adsorption behavior of organic contaminants on dispersed CNTs, which may be a missing link to understanding their environmental behavior and risks, remain unclear yet rarely studied. In this study, the effect of the dispersing agent structure on the adsorption characteristics of BPA (a representative organic contaminant) on dispersed CNTs were investigated using tannic acid (TA), sodium dodecylbenzenesulfonate (SDBS), and gallic acid (GA) as model dispersing agents. Our results showed that at low dispersing agent concentrations, adsorption of TA could lead to higher CNT suspension than adsorption of SDBS and GA due to greater steric hindrance. However, the presence of TA reduced the adsorption of BPA due to strong competitive adsorption on dispersed CNTs. At high concentrations of TA, the suspension of CNTs was reduced by the "bridging effect," in which adjacent dispersed CNTs form hydrogen bonds and re-aggregate. However, the adsorption of BPA dramatically increased due to the enhanced partition of BPA into pseudomicelles of TA on dispersed CNTs, as indicated by the significantly increased index of heterogeneity at high TA concentration. Transmission electron microscopy images confirmed the formation of TA pseudomicelles. This study highlights the key role of the dispersing agent structure on CNT dispersion and adsorption of organic contaminants. The high mobility and transport of CNT-adsorbed contaminants may lead to higher environmental risks compared with aggregated CNTs.

Simultaneous determination of dissolved phenanthrene and its metabolites by derivative synchronous fluorescence spectrometry with double scans method in aqueous solution.

A simple and sensitive derivative synchronous fluorescence spectrometry with double scans (DS-DSFS) method was developed for simultaneous determination of dissolved Phenanthrene (Phe) and its metabolites 1-hydroxy-2-naphthoic acid (1H2NA) and salicylic acid (SA) in aqueous solution. The value of 69 nm was selected as the optimal Δλ conditions for Phe and 1H2NA, and the Δλ value of 55 nm was selected for SA. The overlapping fluorescence emission spectra of Phe, 1H2NA and SA were resolved by DS-DSFS. The signals detected at wavelength of 296 nm for Phe, 352 nm for 1H2NA and 307 nm for SA vary linearly when the concentrations in the range of 4.0-1.0 × 103 µg L-1, 4.0-1.2 × 103 µg L-1 and 4.0-8.0 × 102 µg L-1, respectively. The detection limits were 0.08, 0.07 and 0.88 µg L-1 for Phe, 1H2NA and SA, with the relatively standard deviations less than 5.0%. The established method was successfully applied in the determination of Phe and the metabolites during the biodegradation of dissolved Phe in the lab. It was evidenced that the method has potential for the in situ investigation of PAH biodegradation.