As ZnO nanoparticles have been applied in many fields, their biological risks on human health, of course, are worthy of our attention. Whether ZnO NPs have the risk and how colonic cells respond to the invaded ZnO NPs are still unknown. Herein, we evaluated the biological effects of ZnO NPs on colonic mucosal cells by in vitro and in vivo methods. IMCE cells, with APC mutation but phenotypically normal, demonstrated hyperproliferation through activating the CXCR2/NF-κB/STAT3/ERK and AKT pathways when exposed to ZnO NPs for 24 h. Long-term exposure of ZnO NPs resulted in the malignant transformation of IMCE cells, showing the morphological changes, anchorage-independent cell growth ability. Importantly, IMCE cells exposed to ZnO NPs subcutaneously grew and induced tumorigenesis in nude mice. In conclusion, exposure of ZnO NPs could induce malignant transformation of colonic mucosal cells through the CXCR2/NF-κB/STAT3/ERK and AKT pathways. We suggest that it was necessary to consider using the precautionary principle for gastrointestinal contact nanomaterials.

Lockdown measures to contain COVID-19 pandemic has resulted in a considerable change in air pollution worldwide. We estimate the temporal and diurnal changes of the six criteria air pollutants, including particulate matter (PM₂.₅ and PM₁₀) and gaseous pollutants (NO₂, O₃, CO, and SO₂) during lockdown (25ᵗʰ March – 3ʳᵈ May 2020) across regions of India using the observations from 134 real-time monitoring sites of Central Pollution Control Board (CPCB). Significant reduction in PM₂.₅, PM₁₀, NO₂, and CO has been found in all the regions during the lockdown. SO₂ showed mixed behavior, with a slight increase at some sites but a comparatively significant decrease at other locations. O₃ also showed a mixed variation with a mild increase in IGP and a decrease in the South. The absolute decrease in PM₂.₅, PM₁₀, and NO₂ was observed during peak morning traffic hours (08–10 Hrs) and late evening (20–24 Hrs), but the percentage reduction is almost constant throughout the day. A significant decrease in day-time O₃ has been found over Indo Gangetic plain (IGP) and central India, whereas night-time O₃ has increased over IGP due to less O₃ loss. The most significant reduction (∼40–60%) was found in PM₂.₅ and PM₁₀. The highest decrease in PM was found for the north-west and IGP followed by South and central regions. A considerable reduction (∼30–70%) in NO₂ was found except for a few sites in the central region. A similar pattern was observed for CO having a ∼20–40% reduction. The reduction observed for PM₂.₅, PM₁₀, NO₂, and enhancement in O₃ was proportional to the population density. Delhi’s air quality has improved with a significant reduction in primary pollutants, however, an increase in O₃ was observed. The changes reported during the lockdown are combined effect of changes in the emissions, meteorology, and atmospheric chemistry that requires detailed investigations.

Data from National Health and Nutrition Examination Survey for 2003–2014 for US children aged 6–11 years (N = 2097), adolescents aged 12–19 ears (N = 2642), and adults aged ≥ 20 years (N = 9170) were analyzed to investigate the effects of dietary, demographic, disease, lifestyle, and other factors on concentrations of nine metabolites of polycyclic aromatic hydrocarbons (PAH) in urine. PAHs analyzed were: 1-hydroxynaphthalene, 2-hydroxynaphthalene, 2-hydroxyfluorene, 3-hydroxyfluorene, 9-hydroxyfluorene, 1-hydroxyphenanthrene, 2-hydroxyphenanthrene, 3-hydroxyphenanthrene, and 1-hydroxypyrene. Adults with diabetes were found to have higher adjusted levels of 1-hydroxynaphthalene (4139 vs. 3622 ng/L, p < 0.01) than nondiabetics. Adults with albuminuria had higher adjusted levels of 1-hydroxynaphthalene (4140 vs.3621 ng/L, p < 0.01) and 2-hydroxynaphthalene (6039 vs. 5468 ng/L, p < 0.01) than those without albuminuria. Children with albuminuria had lower adjusted levels of 9-hydroxyfluorene (162 vs. 187 ng/L, p = 0.04), 1-hydroxyphenanthrene (92 vs. 108 ng/L, p < 0.01), and 1-hydroxypyrene (118 vs. 138 ng/L, p < 0.01) than those without albuminuria. The ratios of smoker to nonsmoker adjusted levels for adults varied from a low of 1.4 for 2-hydroxyphenanthrene to a high of 5.6 for 3-hydroxyfluorene. Exposure to environmental tobacco smoke at home was associated with higher levels of most OH-PAHs among children, adolescents, and adults. Consumption of red meat not processed at high temperatures was associated with increased levels of 1-hydroxypyrene (β = 0.00040, p = 0.01), 1-, 2-, and 3-hydroxyphenanthrene, 3-, and 9-hydroxyfluorene. Consumption of red meat processed at high temperatures was associated with increased levels of 2-hydroxynaphthalene (β = 0.00046, p = 0.02) among adults. Consumption of fish processed at high temperatures was associated with decreased levels of 1-hydroxynaphtahlene (β = − 0.00088, p < 0.01), 2-, 3-, and 9-hydroxyfluorene, 1-, 2-, and 3-hydroxyphenanthrene. Among adults, alcohol consumption and caffeine may be associated with increased levels of certain OH-PAHs. Oxidative stress and inflammation associated with exposure to PAHs are associated with albuminuria and have the potential to lead to the development of diabetes.

Soils in urban and industrial areas, especially in larger metropolitan areas such as the Ruhr area, Germany, are commonly characterized by severe anthropogenic overprinting due to urbanization processes including land development measures. Such urban soils often contain various anthropogenic substrate admixtures, like ash, coal, tailings, building rubble, industrial waste materials, as well as urban dust, soot, fly ash, and others. These admixtures often carry higher contents of pollutants such as polycyclic aromatic hydrocarbons (PAH). Whereas elevated PAH concentrations are commonly attributed to non-point pyrogenic carbon sources like soot and particulate matter, petrogenic PAH sources are still largely neglected in this context.In this study, an extended sample set of 62 samples of PAH source materials and urban soils containing anthropogenic substrate components was investigated by combining extended PAH analysis of 59 PAH, alkylated PAH distributions and benzene polycarboxylic acid (BPCA) analysis with regard to petrogenic and pyrogenic PAH source identification. For more reliability of source apportionment by a more integrative signal, the alkylated PAH distributions of different PAH groups were combined according to their degrees of alkylation. Based on this combination, a new PAH alkylation index (ΣC0/(ΣC0+ΣC2)) was derived, which considers, in contrast to commonly used single PAH ratios, a series of non-alkylated and alkylated PAH.By comparison of this PAH alkylation index with the degree of aromatic condensation a new robust and economic method for identifying petrogenic, pyrogenic and mixed PAH sources within soil samples and sediments was developed. It is shown that coal and coal ash particles are a not negligible PAH source in urban soils of mining-dominated regions and can make up a large proportion of the anthropogenic substrate components encountered.Further analyses of samples with defined levels of petrogenic and pyrogenic PAH are necessary to finally evaluate the usefulness of this proposed new PAH-BPCA approach.

In Dhaka, Bangladesh, fine particulate matter (PM₂.₅) air pollution shows strong seasonal trends, with significantly higher mean concentrations during winter than during the monsoon (winter = 178.1 μg/m³ vs. monsoon = 30.2 μg/m³). Large-scale open burning of post-harvest agricultural waste across the Indo-Gangetic Plain is a major source of PM₂.₅ air pollution in northern India during the non-monsoon period. This study evaluates the extent to which the seasonal differences in PM₂.₅ pollution concentrations in Dhaka are accounted for by biomass-burning vs. fossil-fuel combustion sources. To assess this, an index was developed based on elemental potassium (K) as a marker for biomass particulate matter, after adjusting for soil-associated K contributions. Alternatively, particulate sulfur was employed as a tracer index for fossil-fuel combustion PM₂.₅. By simultaneously regressing total PM₂.₅ on S and adjusted K, the PM₂.₅ mass for each day was apportioned into: 1) fossil-fuels combustion associated PM₂.₅; 2) biomass-burning associated PM₂.₅; and, 3) all other PM₂.₅. The results indicated that fossil-fuel combustion contributed 21.6% (19.5 μg/m³), while biomass contributed 40.2% (36.3 μg/m³) of overall average PM₂.₅ from September 2013 to December 2017. However, the mean source contributions varied by season: PM₂.₅ in Dhaka during the monsoon season was dominated by fossil-fuels sources (44.3%), whereas PM₂.₅ mass was dominated by biomass-burning (41.4%) during the remainder of the year. The contribution to PM₂.₅ and each of its source components by transport of pollution into Dhaka during non-monsoon time was also evaluated by: 1) Conditional bivariate (CBPF) and pollution rose plots; 2) Concentration weighted trajectories (CWT), and; 3) NASA satellite photos to identify aerosol loading and fire locations on high pollution days. The collective evidence indicates that, while the air pollution in Dhaka is contributed to by both local and transboundary sources, the highest pollution days were dominated by biomass-related PM₂.₅, during periods of crop-burning in the Indo-Gangetic Plain.

Biochar produced from water hyacinths (Eichhornia crassipes) has been demonstrated to be an effective adsorbent for the removal of certain heavy metals and as a means of control for this highly invasive species. This study involved examined the Cd²⁺ sorption dynamics of an alginate encapsulated water hyacinth biochar (BAC) generated at different temperatures and modified using ferric/ferrous sulfate (MBAC). The maximum Cd²⁺ sorption occurred at a pH of 6 and at a solution temperature of 37 °C. Sorption equilibria for the biochar-alginate capsule (BAC) and modified biochar-alginate capsule (MBAC) treatments fit both the Langmuir (R² = 0.876 to 0.99) and Freundlich (R² = 0.849 to 0.971) equations. Langmuir isotherms had a better fit than the Freundlich isotherms, with maximum sorption capacities ranging from 24.2 to 45.8 mg Cd²⁺ g⁻¹. Larger KL values in Freundlich modeling suggest strong bonding of the BAC and MBAC sorbents to Cd²⁺, with values of KL in the MBAC treatments ranging between 31 and 178% greater than the BAC treatments. Cd²⁺ sorption followed pseudo first-order kinetics (R² = 0.926 to 0.991) with greater efficiency of removal using treatments with biochar generated at temperatures >500 °C. Results from this study highlight the potential for biochar-alginate capsules derived from water hyacinth to be effective for the removal of Cd²⁺ from wastewaters.

Tris (1,3-dichloro-2-propyl) phosphate (TDCPP) is a type halogenated organophosphate flame retardants (OPFRs), which has been identified as contaminants of emerging concern (CECs). The use and production of OPFRs began to increase gradually when brominated flame retardants (BFRs) were banned. Halogenated OPFRs, especially TDCPP have been considered to lead to mutagenicity and carcinogenesis and major concerns have been raised regarding their toxicity. In this study, the toxicity effects and mechanisms of TDCPP were summarized and ecological risk assessment was made regarding its potential impact on freshwater organisms. TDCPP has been widely detected in ecosystems throughout the world, with observed toxicity effects on both humans and freshwater organisms. Inhalation of the dust was found to be the main exposure for humans. TDCPP could be metabolized in the human body, and medium stability was achieved in human body with the main metabolite BDCPP. Aside from mutagenicity and carcinogenesis, TDCPP was also found to have the potential for endocrine disruption and impairing the human reproductive system. Furthermore, this study reviewed the results of previous toxicity experiments, including acute toxicity, growth and development toxicity, neurotoxicity, and hepatotoxicity in freshwater organisms. Risk assessment was made using the safety threshold method by comparing the toxicity data with the exposure data in freshwater. HC₅ (hazardous concentration for 5% of organisms) derived based on traditional endpoints of acute toxicity LC₅₀ (median lethal concentration) or EC₅₀ (concentration for 50% of maximal effect) was 877 μg/L. This value was much higher than the exposure concentration levels in the surface water with EXD₉₀ (exposure data with cumulative probability 90%) of 65.22 ng/L. However, based on the growth and development toxicity data, the derived HC₅ was 33.33 ng/L and the calculated MOS (margin of safety) was below 1. Therefore, the results validated the fact that the ecological risk of TDCPP could not be neglected for its growth and development toxicity.

This work discusses the identification of the transformation products (TPs) generated during the photolytic degradation of dextromethorphan (DXM) and its metabolite dextrorphan (DXO), under simulated solar radiation in aqueous solutions (Milli-Q water and river water) in order to determinate its behavior into the aquatic environment. Tentative identification of the TPs was performed by liquid chromatography/quadrupole time-of-flight mass spectrometry (LC/QTOF-MS), following a suspect screening approach. The use of high resolution-mass spectrometry (HRMS) allowed the tentative identification of DXM and DXO photoproducts based on the structure proposed by an in silico software, the accurate mass measurement, the MS/MS fragmentation pattern and the molecular formula finding. A total of 19 TPs were found to match some of the accurate masses included in a suspect list, and they were all tentatively identified by their characteristic MS-MS fragments. Most of the TPs identified showed a minor modified molecular structure like the introduction of hydroxyl groups, or demethylation. The time-evolution of precursors and TPs were monitored throughout the experiments, and degradation kinetics were presented for each analyte. Finally, the occurrence of DXM, DXO, and their tentatively proposed photodegradation TPs was evaluated in both surface and wastewater. In all real matrices, the results showed that the highest concentration was detected for DXO, followed by TP-244 (N-desmethyldextrorphan) and DXM.

Previous research has shown that Stenotrophomonas has the ability to reduce Cr(VI). In this study, we determined whether the reduction capacity of Cr(VI) is conserved in Stenotrophomonas rhizophila DSM14405ᵀ, a plant-growth-promoting rhizobacterium (PGPR). Our results show that S. rhizophila DSM14405ᵀ displays high Cr(VI) resistance at a minimal inhibitory concentration of 1000 mg/L. Furthermore, it completely reduced 50 mg/L Cr(VI) in 28 h at pH 7.5 at 30 °C. The results of X-ray photoelectron spectroscopy and high performance liquid chromatography coupled to inductively coupled plasma mass spectrometry analysis confirmed the ability of S. rhizophila DSM14405ᵀ to convert Cr(VI) to Cr(III), and indicated the adsorption and intracellular accumulation of Cr(III). Transcriptomic analysis revealed that in the presence or absence of Cr(VI), transcriptomes upon short-term exposure showed more differentially expressed genes than those after long-term exposure. GO and KEGG analyses showed that most of the differentially expressed genes were related to Cr(VI) resistance, including genes related to iron homeostasis, central metabolism, DNA repair and anti-oxidative stress, and sulfur metabolism. Highly Cr(VI)-resistant and reductive abilities of this PGPR strain render it a suitable candidate for combined plant-microbe remediation of chromium contaminants from soil.

The radial transport of cadmium (Cd) is essential for Cd influx in roots. The role of radial transport pathway on the Cd translocation from root to shoot among wheat genotypes are still poorly understood. This study explored the role of apoplastic and symplastic pathway on root Cd uptake and root-to-shoot translocation in Zhenmai 10 (ZM10, high Cd in grains) and Aikang 58 (AK58, low Cd in grains). Under Cd treatment, the deposition of Casparian strips (CSs) and suberin lamellae (SL) initiated closer to the root apex in ZM10 than that in AK58, which resulted in the lower Cd concentration in apoplastic fluid of ZM10. Simultaneously, Cd-induced expression levels of genes related to Cd uptake in roots were significantly higher in AK58 by contrast with ZM10, contributing to the symplastic Cd accumulation in AK58 root. Moreover, the addition of metabolic inhibitor CCCP noticeably decreased the Cd accumulation in root of both genotypes. Intriguingly, compared to ZM10, greater amounts of Cd were sequestrated in the cell walls and vacuoles in roots of AK58, limiting the translocation of Cd from root to shoot. Furthermore, the elevated TaHMA2 expression in ZM10 indicates that ZM10 had a higher capacity of xylem loading Cd than AK58. All of these results herein suggest that the radial transport is significant for Cd accumulation in roots, but it cannot explain the difference in root-to-shoot translocation of Cd in wheat genotypes with contrast Cd accumulation in grains.