An alarming rise of micro-nano plastics (MNPs) in environment is currently causing the biggest threat to biotic and abiotic components around the globe. These pollutants, apart from being formed through fragmentation of larger plastic pieces and are also manufactured for commercial usage. MNPs enter agro-ecosystem, wildlife, and human body through the food chain, ingestion or through inhalation, causing blockage in the blood-brain barrier, lower fertility, and behavioural abnormalities among other problems. Hence, it becomes essential to develop novel procedures for remediation of MNPs. Among the numerous existing methods, microbial remediation promises to degrade/recover MNPs via a green route. Since microbial remediation processes mostly depend upon biotic and abiotic factors such as (temperature, pH, oxidative stress, etc.), it becomes easy to influence changes in the plastic pollutants. Hence, with the help of recent technologies, a complete degradation/removal of MNPs can be expected by utilizing the respective carbon content as energy sources for growth of microorganisms. In this review, considering the urgent environmental need, the impact of micro-nano plastics on ecosystem along with its corresponding degradation mechanisms has been brought out. Also, importance of the various recent research approaches in MNPs remediation is highlighted. Finally, the role of enzyme and membrane technology, nanoparticle technology, and metagenomics in remediation of MNPs are discussed for the first time in detail to bring out a novel remedy for the environment.

Sludge is an inevitable by-product of municipal wastewater treatment processes, and its high moisture content poses a major challenge for its subsequent treatment and disposal. Previous studies have explored the effects of applying modified corn-core powder (MCCP) on dewatering sludge. Here, we characterized the effects of applying both MCCP and sludge-based biochar (SBB) on dewatering sludge. Analysis of the anti-shear ability of SBB revealed that SBB was a skeleton builder with high compressive strength, demonstrating that SBB could maintain the permeability of sludge under high-pressure filtration processes and facilitate the flow of bound water. Dissipative particle dynamics (DPD) was used to simulated the sludge flocculating process and verify the feasibility of the experiment. As the simulation progressed, the reaction in the sludge network reached equilibrium and the simulated structure of the sludge became loose. The dewatering performance and physicochemical properties of the treated sludge were studied to further characterize the effect of this combined technology. Compared with MCCP-sludge, MCCP&SBB-sludge, which was treated by 20% DS (mass of dry solids in sludge) of SBB and 20% DS of MCCP, achieved superior dewaterability. This combined method reduced the specific resistance of filtration by 76% and enlarged the net sludge solids yield by 138%. Further study of the properties of MCCP&SBB-sludge revealed a loose structure that resembled the structure recovered by the simulation, suggesting that the DPD simulation method simulated the sludge flocculating process successfully. Therefore, the combined application of MCCP and SBB was superior for sludge dewatering because of the synergistic effects of MCCP and SBB.

No information is available on the long-term effects on thyroid and growth hormones of children exposed to phthalate-tainted products, despite the infamous 2011 Taiwan phthalate episode. We investigated estimated daily intake levels and their long-term effects on serum thyroid and growth hormone levels in children.We recruited 166 children (2–18 years old) in three visits who provided specimens and filled out a questionnaire from the Risk Assessment of Phthalate Incident in Taiwan (RAPIT) project study from 2012 to 2016. Morning spot urine samples were analyzed for nine phthalate metabolites. Serum thyroid (triiodothyronine [T₃], thyroxine [T₄], and free T₄) and growth hormone (insulin-like growth factor-1 [IGF-1] and its binding protein 3 [IGF-BP3]) levels were measured. A generalized estimating equation model was used to evaluate associations between phthalate metabolite levels and children’s thyroid and growth hormone levels.The median metabolite levels of monomethyl phthalate (MMP), Σdibutyl phthalate (DBP), and Σdi-(2-ethylhexyl) phthalate (DEHP) at visits 1, 2, and 3 were 6.59, 10.5, and 21.0 ng/mL, 0.15, 0.24, and 0.20 nmol/mL, and 0.15, 0.17, and 0.12 nmol/mL, respectively. After adjusting for potential confounding factors, we found that levels of urinary MMP were negatively associated with T₃ (β = −0.013, p = 0.047), T₄ (β = −0.016, p = 0.006), free T₄ (β = −0.012, p = 0.002), and IGF-BP3 (β = −0.025, p = 0.003). Urinary mono-ethyl phthalate (MEP) was negatively associated with IGF-1 (β = −0.027, p = 0.029) and IGF-BP3 (β = −0.016, p = 0.018). In addition, serum free T₄ was positively associated with urinary mono-2-ethyl-5-hydroxy hexyl phthalate (MEHHP) (β = 0.016, p = 0.043), mono-2-ethyl-5-oxohexyl phthalate (MEOHP) (β = 0.015, p = 0.024), and ΣDEHPm (β = 0.019, p = 0.020).Our findings support the hypothesis that specific phthalates disturb the hemostasis of thyroid and growth hormone levels in children exposed to phthalate-tainted products.

Anaerobic reductive treatment technologies offer cost-effective and large-scale treatment of chlorinated compounds, including polychlorinated dibenzo-p-dioxins and furans (PCDD/Fs). The information about the degradation rates of these compounds in natural settings is critical but difficult to obtain because of slow degradation processes. Establishing a relationship between biotransformation rate and abundance of biomarkers is one of the most critical challenges faced by the bioremediation industry. When solved for a given contaminant, it may result in significant cost savings because of serving as a basis for action. In the current review, we have summarized the studies highlighting the use of biomarkers, particularly DNA and RNA, as a proxy for reductive dechlorination of chlorinated ethenes. As the use of biomarkers for predicting biotransformation rates has not yet been executed for PCDD/Fs, we propose the extension of the same knowledge for dioxins, where slow degradation rates further necessitate the need for developing the biomarker-rate relationship. For this, we have first retrieved and calculated the bioremediation rates of different PCDD/Fs and then highlighted the key sequences that can be used as potential biomarkers. We have also discussed the implications and hurdles in developing such a relationship. Improvements in current techniques and collaboration with some other fields, such as biokinetic modeling, can improve the predictive capability of the biomarkers so that they can be used for effectively predicting biotransformation rates of dioxins and related compounds. In the future, a valid and established relationship between biomarkers and biotransformation rates of dioxin may result in significant cost savings, whilst also serving as a basis for action.

Perfluorohexane sulfonate (PFHxS) has been newly recommended to be added into the Stockholm Convention on persistent organic pollutants (POPs). As one of the major perfluoroalkyl pollutants, its long half-time in human serum and neurotoxicity are cause for significant concern. Although mechanochemical degradation has been evaluated as a promising ecofriendly technology to treat pollutants, the extraordinary stability of poly- and perfluoroalkyl substances (PFASs) raises harsh requirements for co-milling reagents. In the present study, zero-valent iron (ZVI) and ferrate(VI) were for the first time used as the co-milling reagents to degrade PFHxS. When ZVI and ferrate(VI) were used alone, both the degradation and defluorination efficiencies were low. However, after milling at the optimum ratio (ferrate(VI):ZVI = 1:2) for 4 h, the synergistic effect of ZVI and ferrate(VI) resulted in almost complete degradation (100%) and defluorination (95%). Two points can account for this excellent performance: (1) the mechanochemical energy input in the system initiates and prominently promotes related reactions; and (2) the active species generated from the reactions among ZVI, ferrate(VI) and other high-valent iron species will accelerate the process of electron transfer. The sulfonate group comprises the favorable attack sites, as corroborated by both the identified intermediates and quantum chemical calculations. The homolysis of the C–S bond is not only the triggering step, but also the rate-limiting step. In summary, the present work confirms the feasibility and underlying mechanism of the ZVI–ferrate(VI) co-milling system to defluorinate PFHxS, which might be a promising technology to treat PFASs in solid wastes.

F–53B and PFOS are two per- and polyfluoroalkyl substances (PFASs) widely utilized in the metal plating industry as mist suppressants. Recent epidemiological studies have linked PFASs to cardiovascular diseases and alterations in heart geometry. However, we still have limited understanding of the effects of F–53B and PFOS on the developing heart. In this study, we employed a human embryonic stem cell (hESC)-based cardiac differentiation system and whole transcriptomics analyses to evaluate the potential developmental cardiac toxicity of F–53B and PFOS. We utilized F–53B and PFOS concentrations of 0.1–60 μM, covering the levels detected in human blood samples. We demonstrated that both F–53B and PFOS inhibited cardiac differentiation and promoted epicardial specification via upregulation of the WNT signaling pathway. Most importantly, the effects of F–53B were more robust than those of PFOS. This was because F–53B treatment disrupted the expression of more genes and led to lower cardiac differentiation efficiency. These findings imply that F–53B may not be a safe replacement for PFOS.

Sites contaminated by mercury (Hg) from artisanal small-scale gold mine tailings have been found near agricultural land. For the active implementation of the Minamata Convention on Mercury, development of technology for the remediation of Hg contaminated sites is required. This study examined the conditions for the thermal treatment of Hg contaminated tailings at reduced temperature by introducing SnCl₂ as an additive. Thermogravimetric analysis (TGA) was used to identify the possibility of converting typical Hg compounds (HgO, HgS) in the environment to HgCl₂. The operation conditions for thermal treatment such as temperature, retention time, and ratio of [Cl₂]/[Hg] were derived from lab scale experiments using commercial Hg compounds (HgO, HgS), additive (SnCl₂), and tailings. The tailings with Hg content of 26.39 mg-Hg/kg were reduced to 3.87 mg-Hg/kg and 4.57 μg-g/L of leaching concentration through the application of the Korea standard leaching test. Both concentrations were below the standard limit of soil pollution and hazardous waste classification criteria. The sequential extraction procedure was applied to evaluate the Hg stability of residual tailings. The results show that this method will be effective for remediation of small scale Hg contaminated areas.

The new-generation geostationary satellites feature higher radiometric, spectral, and spatial resolutions, thereby making richer data available for the improvement of PM₂.₅ predictions. Various aerosol optical depth (AOD) data assimilation methods have been developed, but the accurate representation of the AOD-PM₂.₅ relationship remains challenging. Empirical statistical methods are effective in retrieving ground-level PM₂.₅, but few have been evaluated in terms of whether and to what extent they can help improve PM₂.₅ predictions. Therefore, an empirical and statistics-based scheme was developed for optimizing the estimation of the initial conditions (ICs) of aerosol in WRF-Chem (Weather Research and Forecasting/Chemistry) and for improving the PM₂.₅ predictions by integrating Himawari-8 data and ground observations. The proposed method was evaluated via two one-year experiments that were conducted in parallel over eastern China. The contribution of the satellite data to the model performance was evaluated via a 2-week control experiment. The results demonstrate that the proposed method improved the PM₂.₅ predictions throughout the year and mitigated the underestimation during pollution episodes. Spatially, the performance was highly correlated with the amount of valid data.

The long-term and large-scale utilization of fertilizers and pesticides in facility agriculture leads to groundwater pollution. However, the coexistence and interactions between organic fertilizers (i.e., organic matter), toxic metals, and pesticides in shallow groundwater have seldom been studied. Thus, the study sought to characterize said interactions via fluorescence, ultraviolet–visible spectroscopy (UV–Vis), and Fourier-transform infrared spectroscopy coupled with two-dimensional correlation spectroscopy and chemometric techniques. The results indicated that groundwater DOM was comprised of protein-, polysaccharide-, and lignin-like substances derived from organic fertilizers. Protein-like substances accounted for the binding of Co, Ni, and Fe, while polysaccharide- and lignin-like substances were mainly responsible for Cr and Mo complexation. Moreover, lignin- and polysaccharide-like substances played a key role in the binding of pesticides (i.e., dichlorodiphenyltrichloroethane [DDT], endosulfan, γ-hexachlorocyclohexane [γ-HCH], monocrotophos, chlorpyrifos, and chlorfenvinphos), rendering the conversion of γ-HCH to β-hexachlorocyclohexane (β-HCH) and the degradation of DDT to dichlorobenzene dichloroethylene (DDE) ineffective. However, the presence of protein-like substances in groundwater benefited the degradation and conversion of γ-HCH and α-endosulfan. Redundancy analyses showed that lignin- and polysaccharide-like matter had the most impacts on the coexistence of DOM with toxic metals and pesticides.

Aspergillus fumigatus is the primary agent of invasive aspergillosis (IA) causing high morbidity and mortality in immunocompromised patients. Triazole resistance in A. fumigatus and its sources have gained wide attention. For several years, environmental fungicides use has been proposed as the major cause for triazole resistance in A. fumigatus. However, there are few studies on azole-resistant A. fumigatus (ARAF) selected by triazole fungicides in agricultural systems. We studied the possible emergence of ARAF in the field after exposure to triazole fungicide tebuconazole. Our results showed that exposure to tebuconazole in soil selects for resistance to triazoles in A. fumigatus. The probability of ARAF developing in soils depends upon the concentrations of tebuconazole after application. We suggest that tebuconazole applications should be minimized to reduce selective pressure for the generation of ARAFs.