Low-molecular-weight organic acids may significantly influence the mobility of metal in environment, but the kinetics are not fully understood and have not been quantified. In this study, the thermodynamic and kinetic effects of citric acid (CA) on the adsorption of Cd(II) and Ni(II) on goethite were investigated using batch-adsorption and stirred-flow experiments. A charge distribution and multisite complexation model (CD-MUSIC) and a thermodynamically based multi-rate kinetic model were employed to describe the adsorption behaviors. Two ternary surface complexes, (≡FeO)₂CitMe and (≡FeOH)₂MeCit²⁻, were involved in the adsorption. In addition, CA differed in its effects on Cd(II) and Ni(II) adsorption, enhancing Cd(II) adsorption but inhibiting Ni(II) adsorption at high levels. Kinetically, in the presence of CA, the adsorption of Cd(II) was faster than that of Ni(II). Increasing CA concentration led to faster Cd(II) adsorption, but resulted in the dissolution of the adsorbed Ni(II), possibly due to the much higher complexation constants of Ni-CA than of Cd-CA in aqueous phase. This finding implied that, in the rhizosphere, high level of CA may lead to more dissolution of Ni(II) than Cd(II); while in acidic ferrosol, CA may alleviate Cd(II) mobility and toxicity. The proposed mechanistic model sheds light on ion partition in the soil environment and may improve predictions thereof.

Soil heavy metal contamination has increasingly become a serious environmental issue globally, nearing crisis proportions. There is an urgent need to find environmentally friendly materials to remediate heavy-metal contaminated soils. With the continuing maturation of research on using biochar (BC) for the remediation of contaminated soil, nano-biochar (nano-BC), which is an important fraction of BC, has gradually attracted increasing attention. Compared with BC, nano-BC has unique and useful properties for soil remediation, including a high specific surface area and hydrodynamic dispersivity. The efficacy of nano-BC for immobilization of non-degradable heavy-metal contaminants in soil systems, however, is strongly affected by plant rhizosphere processes, and there is very little known about the role that nano-BC play in these processes. The rhizosphere represents a dynamically complex soil environment, which, although having a small thickness, drives potentially large materials fluxes into and out of plants, notably agricultural foodstuffs, via large diffusive gradients. This article provides a critical review of over 140 peer-reviewed papers regarding nano-BC-rhizosphere interactions and the implications for the remediation of heavy-metal contaminated soils. We conclude that, when using nano-BC to remediate heavy metal-contaminated soil, the relationship between nano-BC and rhizosphere needs to be considered. Moreover, the challenges to extending our knowledge regarding the environmental risk of using nano-BC for remediation, as well as further research needs, are identified.

Quantifying source apportionment of potentially toxic elements (PTEs) in soils and associated human health risk (HHR) is essential for soil environment regulation and pollution risk mitigation. For this purpose, an integrated method was proposed, and applied to a dataset consisting of As, Cd, Cr, Cu, Hg, Ni, Pb, Se, and Zn in 273 soil surface samples. Positive matrix factorization (PMF) was used to quantitatively examine sources contributions of PTEs in soils; and the HHR arising from the identified source was determined by combining source profiles and health risk assessment; at last, sequential Gaussian simulation (SGS) was used to identify the areas with high HHR. Four sources were identified by PMF. Natural and agricultural sources affected all 9 PTEs contents with contributions ranging from 19.2% to 62.9%. 41.9% of Cd, 40.8% of Pb, 58.6% of Se, and 29.8% of Zn were controlled by industrial and traffic emissions. Metals smelting and mining explained 35.5%, 30.5%, and 24.9% of Cr, Cu, and Ni variations, respectively. Hg was dominated by atmospheric deposition from coal combustion and coking (58.7%). The mean values of the total non-carcinogenic risks of PTEs were 1.55 × 10⁻¹ and 9.40 × 10⁻¹ for adults and children, and the total carcinogenic risk of PTEs had an average value of 8.86 × 10⁻⁵. Based on source-oriented HHR calculation, natural and agricultural sources were the most important factor influencing HHR, explaining 51.0% and 49.1% of non-carcinogenic risks for children and adults, and 44.2% of carcinogenic risk. SGS indicated that 1.1% of the total area was identified as hazardous areas with non-carcinogens risk for children.

Heavy metal contamination has been threatening the health of human beings. To decrease the bio-toxicity of heavy metals, a thiol-functionalized nano-silica (SiO₂-SH) was adopted to remediate the soil contaminated by lead (Pb), cadmium (Cd) and copper (Cu). The remediation effect of SiO₂-SH on contaminated soils was investigated by the uptake of the heavy metals into lettuce and pakchoi in pot experiment. The bio-toxicity of the SiO₂-SH was evaluated, and its immobilization mechanisms were proposed by the fraction distribution of Cd, Pb and Cu. It was found that the SiO₂-SH can significantly reduce the uptake of Cd, Pb, Cu into pakchoi by 92.02%, 68.03%, 76.34% and into lettuce by 89.81%, 43.41%, 5.76%, respectively. The chemical species analyses of Cd, Pb, Cu indicate SiO₂-SH can transform the heavy metal in acid soluble states into reducible fraction and oxidizable fraction, thereby inhibiting the extraction of heavy metals into soil solution. The concentrations of microbial biomass carbon, organic matter, and cation exchange capacity of the soil increased while the soil bulk density decreased after remediation. Those changes demonstrate that SiO₂-SH not only has no bio-toxic impact on the soil environment but also improves the soil environment, which proves the prepared SiO₂-SH is environmental-friendly. The SiO₂-SH could be a promising amendment for heavy metal contaminated soils.

Microplastic (MP) pollution in the environment has aroused great concern. However, our knowledge of MP abundance and distribution in soil environment is scarce. This work investigated the MPs in the farmland and grassland at a remote area of China, namely, the eastern area of the Qinghai–Tibet Plateau (QTP). The average numbers of MPs were 53.2 ± 29.7 and 43.9 ± 22.3 items/kg in shallow and deep soil, respectively, from 35 soil samples. A remarkable difference in MP abundances was observed among soil samples from mulch farmland, greenhouses, farmland without covering, and grassland. The MPs were mostly in the form of a film and transparent in color in this study. The dominant polymers of MPs in the soil samples were polyester (PE) and polypropylene (PP). This study revealed the characteristics of MP distribution among different land use at the QTP, and MPs may stem from the fragmentation of plastic mulch in farmland soil. Notably, MP abundance increased with the increase in mulching time in facility agriculture. Additionally, human disturbances and increased mulching time in facility agriculture promote the fragmentation of soil MPs. This study provides important data for follow-up research on MPs in a plateau terrestrial ecosystem.

The interactive effects of elevated atmospheric CO₂ and nanoparticles (NPs) on the structure and function of soil bacterial community remain unknown. Here we compared the impacts of CeO₂ (nCeO₂) and Cr₂O₃ (nCr₂O₃) nanoparticles on the taxonomic compositions and functional attributes of bacterial communities under elevated CO₂ (eCO₂). The stimulated enzyme activities (dehydrogenase, acid phosphatase and urease), increased microbial biomass carbon (MBC), and higher bacterial alpha-diversity were observed under the combined effects of eCO₂ and NPs compared to the single NP treatment, indicating eCO₂ could mitigate the adverse effect of NPs on soil microorganisms. NPs and eCO₂ are important factors influencing the alpha- and beta-diversity (17% and 18% of variations were explained) as well as functional profile (20% and 26% of variations were explained) of bacterial communities. Rising CO₂ level promoted the resilience of NP-resistant bacterial populations, primarily the members of Alphaproteobacteria, Gammaproteobacteria and Bacteroidia, which are also characterized by the fast carbon use capability. Moreover, the significantly (P < 0.05) higher metabolic quotient (qCO₂), reduced available carbon and overrepresented carbon metabolism genes at eCO₂vs. ambient CO₂ (aCO₂) indicate the acceleration of available carbon turnover in NP-exposed soils. Correlation analysis revealed that mitigation of NPs toxicity by eCO₂ could be attributed to the remarkable decline of bioavailable metals disassociated from NPs and available carbon level, as well as promotion of the rapid carbon-metabolizing microbes. Our study pointed out the positive role of eCO₂ in alleviating the adverse effect of NPs on microbiological soil environment, and results can serve as important basis in establishing guidelines for lowering the ecotoxicity of NPs.

Propylparaben is widely used as a preservative in pharmaceuticals and personal care products and is ultimately excreted by the human body. Thus, propylparaben reaches sewage and enters the soil environment by sludge fertilization and wastewater irrigation. However, there are few existing studies on the toxicity and risks of such chemicals in terrestrial environments. In this study, a multispecies bioassay for propylparaben was performed and protective concentrations (PCs) were derived based on toxicity values by probabilistic ecological risk assessment. Acute and chronic bioassays were conducted on 11 species in eight taxonomic groups (Magnoliopsida, Liliopsida, Clitellata, Entognatha, Entomobryomorpha, Chromadorea, Chlorophyceae, Trebouxiophyceae). Based on the toxicity values calculated, the PC₉₅ values for acute and chronic SSDs were 13 and 6 mg/kg dry soil, respectively. Toxicity varied among taxa, with soil algae emerging as the most sensitive to propylparaben. This may be attributable to differences in exposure pathways among species. The exposure pathway of propylparaben can be altered by adsorption to soil particles. As parabens are presently under-regulated globally in terms of their environmental effects, our findings can serve as the basis to propose standard values for environmental protection.

Many reliable studies have provided evidence of microplastic ingestion by soil organisms. However, further research is required to determine the edible size of microplastics, especially given the ubiquity of microplastics and their adverse effects on the soil environment. Determining the size range of microplastics that can be ingested by soil organisms is crucial for the prediction of the exposure route and toxicity mechanisms of microplastics in soil. Springtails, organisms prevalent in a wide variety of soil ecosystems, can ingest or transport microplastics; however, direct evidence for this has not been reported. To address this knowledge gap, we designed dietary exposure experiments under laboratory conditions, using the springtail species Folsomia candida. The springtails were administered polyethylene microplastics in three different sizes (2, 34, and 66 μm) via their food for a short period of time; we further observed the intestinal presence of microplastics via fluorescence microscopy to determine the maximum edible size. We evaluated the effects of ingested microplastics on springtails by quantifying their moving behavior. The results show that the edible size of microplastics is < 66.0 ± 10.9 μm, and microplastics smaller than this can significantly reduce the velocity and distance of springtail movement by 74% ± 38% compared with the control group. Based on this finding, the broader fate and toxicity of microplastics in soil environments can be estimated. Furthermore, the average velocity and distance of springtail movement decreases in response to microplastic ingestion, highlighting the negative effects of microplastics on soil organisms.

The human pathogenic bacteria (HPB) in animal feces may disseminate to agricultural soils with their land application as organic fertilizer. However, the knowledge about the impacts of different sources and rates of animal manures on the temporal changes of soil HPB remains limited, which hamper our ability to estimate the potential risks of their land application. Here, we constructed an HPB database including 565 bacterial strains. By blasting the 16 S rRNA gene sequences against the database we explored the occurrence and fate of HPB in soil microcosms treated with two rates of swine, poultry or cattle manures. A total of 30 HPB were detected in all of manure and soil samples. Poultry manure at the high level obviously improved the abundance of soil HPB. The application of swine manure could introduce concomitant HPB into the soils. Of which, Pseudomonas syringae pv. syringae B728a and Escherichia coli APEC O78 may deserve more attention because of their survival for a few days in manured soils and being possible hosts of diverse antibiotic resistance genes (ARGs) as revealed by co-occurrence pattern. Bayesian source tracking analysis showed that the HPB derived from swine manure had a higher contribution to soil pathogenic communities than those from poultry or cattle manures in early days of incubation. Mantel test together with variation partitioning analysis suggested that bacterial community and soil physicochemical properties were the dominant factors determining the profile of HPB and contributed 64.7% of the total variations. Overall, our results provided experimental evidence that application of animal manures could facilitate the potential dissemination of HPB in soil environment, which should arouse sufficient attention in agriculture practice and management to avoid the threat to human health.

Perfluorooctanoic acid (PFOA) is an emerging persistent organic pollutant which has been identified at significant levels in soils. Existed ecotoxicological studies have mainly employed earthworms to evaluate the toxicity of PFOA. However, little information do we know about the toxicity of PFOA regarding soil microorganisms. Accordingly, the adverse effects of PFOA on microbial activity in a wheat soil under four fertilization treatments were investigated in this study. The microcalorimetric results revealed that the toxicity of PFOA on soil microbial activity in four treatments followed a descending sequence: Control (no fertilization), NK (no P fertilizer, but N and K fertilizers were used), PK (no N fertilizer, but P and K fertilizers were used), and NPK (N, P and K fertilizers were used). The soil sample with higher available P content had higher resistant to PFOA. There were significant differences in urease activity and alkaline phosphatase activity among the four fertilization treated soils. Molecular modeling studies clearly demonstrated that the binding of PFOA with alkaline phosphatase was more stable than with urease through electrostatic interaction, van der Waals force, and hydrogen bonds. These results are expected to provide more comprehensive information in toxicity of PFOA in soil environment.