Metal enrichment of road dust is well characterized but available data on the bioaccessibility of metals in particle size fractions relevant to human respiratory health remain limited. The study goal was to investigate the bioaccessibility of platinum group elements (PGE), which are used as catalysts in automotive exhaust converters, in the inhalable fraction of road dust. Street sweepings were provided by the City of Toronto, Canada, collected as part of its Clean Roads to Clean Air program.The particle size relevance of road dust for inhalation exposures was confirmed using a laser diffraction particle size analyzer (mean Dx(50): 9.42 μm). Total PGE were determined in both bulk and inhalable fractions using nickel sulfide (NiS) fire-assay and instrumental neutron-activation analysis (INAA). PGE lung solubility was examined for the inhalable fraction using Gamble’s extraction. Sample digests were co-precipitated with Te-Sn, to pre-concentrate and isolate PGE, prior to their measurement using inductively coupled plasma mass spectrometry (ICP-MS).Total PGE concentrations were enriched in the inhalable fraction of road sweepings. Geomean concentrations in the inhalable fraction were: palladium (Pd) (152 μg/kg), platinum (Pt) (55 μg/kg), rhodium (Rh) (21 μg/kg) and iridium (Ir) (0.23 μg/kg). Osmium (Os) concentrations were below the limit of detection (LOD). Bioaccessible PGEs (n = 16) using Gamble’s solution were below LOD for Ir and ruthenium (Ru). For the remainder, the geomean % bioaccessibility was highest for platinum (16%), followed by rhodium (14%) and palladium (3.4%). This study provides evidence that PGE in road dust are bioaccessible in the human lung.

Analysis of observed PM₂.₅ in Beijing since 2009 reveals that winter haze over North China Plain (NCP) peaked in 2012 and 2013 and there was an improvement in air quality until 2016. The variation of wintertime PM₂.₅ from 2009 to 2016 is influenced by both emission changes and meteorology conditions, and we quantified the relative contributions from these two aspects. Sensitivity simulation by GEOS-Chem suggested that emission reductions over NCP in 2013–2017 caused 10% decrease of regional mean PM₂.₅ concentration in 2016 winter compared to 2012 winter level. We removed emission influence on PM₂.₅ to get PM₂.₅ that influenced by meteorology (met-influenced PM₂.₅). For met-influenced PM₂.₅, compared to original-observed PM₂.₅(the US Embassy data), percentage of clean days (daily PM₂.₅ ≤ 75 μg m⁻³) decreases while that of polluted (75 μg m⁻³ < daily PM₂.₅ ≤150 μg m⁻³) and heavily polluted (150 μg m⁻³ < daily PM₂.₅ ≤ 250 μg m⁻³) days increases. However, proportion of extremely polluted (daily PM₂.₅ > 250 μg m⁻³) days stays unchanged, even if emission reduction is doubled, indicating that the extremely polluted situation over NCP is dominated by meteorological conditions, and emission control from 2013 to 2017 has little effects on the extremely polluted days. We developed an effective haze day index (HDI) to represent the weather conditions conducive to haze days. HDI is constructed based on the normalized near surface meridional wind (V850), temperature difference (δT) between near surface (850 hPa) and upper atmosphere (250 hPa), and the relative humidity at 1000 hPa (RH1000). HDI is skillful to detect 72% of the severe haze days (daily PM₂.₅ > 150 μg m⁻³). On average, the anomalously high V850 is the main cause of severe haze, while in 2012 winter, RH1000 favorable for secondary aerosols’ formation is the largest contributor to haze.

Black carbon and total organic carbon (TOC) along with organochlorines (OCs) were analyzed in soils from four sampling zones of Lesser Himalayan Region based on source proximity/anthropogenic influences along the altitude. CTO-375 method was used for BC analysis while OCs were analyzed by GC-MS/MS system. BC and TOC ranged between 0.16–1.77 and 6.8–41.3 mg g−1 while those of OCPs and PCBs ranged between 0.69 and 5.77 and 0.12–2.55 ng g−1, respectively. ∑DDTs were the dominant (87.9%) among OCPs while tri- and tetra- (65.5%) homologue groups among PCBs. Hexa-PCBs, however also showed higher contribution (20.4%) in the region. Source diagnostic ratios of DDE + DDD/DDT (0.1–1.53) indicated both fresh and old input while α-HCH/γ-HCH (0.19–2.49) showed presence of lindane in the region. Higher concentration of OCs were observed in Zone C at altitudinal range of 737–975 masl that are close to the human influences and potential sources of POPs. The results of linear regression analysis revealed potential input of BC in soil distribution of OC concentrations in the region.

The Red River Delta is a major agricultural production area of Vietnam with year-round use of pesticides for paddy rice cultivation and other production systems. The delta is protected from flooding, storm surges and saline water intrusion by a sophisticated river and sea-dyke system. Little is known about the effects of such a dyke system on pesticide pollution in the enclosed landscape. Our aim was to address this gap by i) determining pesticide prevalence in soils and sediments within a dyked agricultural area, and by ii) assessing whether and to which degree this dyke system might affect the spatial distribution of pesticides. After sampling paddy rice fields (topsoil) and irrigation ditches (sediment) perpendicular to the dyke in Giao Thuy district, we analysed 12 of the most commonly used pesticides in this area. In soils, we detected most frequently isoprothiolane (100% detection frequency), chlorpyrifos (85%) and propiconazole (41%) while in sediments isoprothiolane (71%) and propiconazole (71%) were most frequently found. Maximum concentrations reached 42.6 μg isoprotiolane kg⁻¹ in soil, and 35.1 μg azoxystrobin kg⁻¹ in sediment. Our results supported the assumption that the dyke system influenced residue distribution of selected pesticides. More polar substances increasingly accumulated in fields closer to the sea-dyke (R² = 0.92 for chlorpyrifos and 0.51 for isoprothiolane). We can thus support initiatives from local authorities to use the distance to dykes as a mean for deliniating zones of different environmental pollution; yet, the degree at which dykes influence pesticide accumulation appear to be compound specific.

Polar regions are fragile ecosystems threatened by both long-range pollution and local human contamination. In this context, the environmental distribution of the Personal Care Products (PCPs) represent a major knowledge gap. Following preliminary Antarctic studies, Fragrance Materials (FMs) were analyzed in the seawater and snow collected in the area of Ny-Ålesund, Svalbard, to investigate local and long-range contamination. Polycyclic Aromatic Hydrocarbons (PAHs), including Retene, were determined in parallel to help the identification of the governing processes. Concentrations of FMs up to 72 ng L⁻¹ were detected in the surface snow near the settlement and at increasing distances, in relation to the prevailing winds. PAHs follow a similar scheme, with levels of Retene up to 1.8 μg L⁻¹, likely deriving from the occurrence of this compound in the coal dust due to the previous mining activities in the area. The snow seasonal deposition of FMs and PAHs was estimated in a snowpit dug at the top of the Austre Brøggerbreen glacier, indicating the long-range atmospheric transport (LRAT) of these compounds.

The increasing adoption of intelligent transportation system (ITS) data in smart-city initiatives worldwide has offered unprecedented opportunities for improving transportation air quality management. In this paper, we demonstrate the effective use of ITS and other traffic data to develop a link-level and hourly-based dynamic vehicle emission inventory. Our work takes advantage of the extensive ITS infrastructure deployed in Nanjing, China (6600 km2) that offers high-resolution, multi-source traffic data of the road network. Improved than conventional emission inventories, the ITS data empower the strength of revealing significantly temporal and spatial heterogeneity of traffic dynamics that pronouncedly impacts traffic emission patterns. Four urban districts account for only 4% of the area but approximately 30%–40% of vehicular emissions (e.g., CO2 and air pollutants). Owing to the detailed resolution of road network traffic, two types of emission hotspots are captured by the dynamic emission inventory: those in the urban area dominated by urban passenger traffic, and those along outlying highway corridors reflecting inter-city freight transportation (especially in terms of NOX). Fine-grained quantification of emissions reductions from traffic restriction scenarios is explored. ITS data-driven emission management systems coupled with atmospheric models offer the potential for dynamic air quality management in the future.

Although the aggregation of graphene oxide (GO) has been widely researched, the influence of the GO size on the homoaggregation behavior and its interaction with environmental media are still unexplored. In this work, critical coagulation concentration (CCC) values for GO with different sizes, from micro to nanosheet, were measured with NaCl and CaCl₂ electrolytes, and the results indicated that GO with the largest size presented the smallest CCC value. Aluminum oxide (Al₂O₃) was selected as a natural solid particle representative to mimic the interaction between GO and environmental media. Batch experiments were conducted in solution with different pH and ionic strength. Results indicated that the attachment capacity of large GO onto Al₂O₃ particles was greater than that of small GO. The experimental data were well fitted with Freundlich model. The electrostatic attraction and hydrogen-bonding interaction dominated the interaction process between GO and Al₂O₃. These findings are important for better understanding in the environmental fate and transport of GO.

As a result of human activities, the pollution of metals is becoming ubiquitous in the environment. Among various toxicological mechanisms of action, metals have been considered as endocrine-disrupting chemicals (EDCs) through interference with steroid receptors. However, information regarding the potential endocrine disruption of metals on glucocorticoid receptor (GR) and mineralocorticoid receptor (MR) is especially scarce. In this study, a total of 16 metals were assessed for their GR/MR activities using luciferase reporter gene assay. None of the tested metals exhibited GR or MR agonistic activity, but a total of 7 and 5 candidate metals showed obvious GR and MR antagonistic properties, respectively. All 7 GR antagonistic metals [ BaCl₂, CoCl₂, CuCl₂, Pb(NO₃)₂, LiCl, SnCl₂ and ZnCl₂] inhibited glucocorticoid-responsive gene GILZ expression in J774A.1 cells. Further investigations indicated that the 5 MR antagonistic metals [ CdCl₂, Pb(NO₃)₂, LiCl, MnCl₂ and SnCl₂] antagonized aldosterone-inhibited hepatocellular carcinoma cell proliferation. Among these metals, Pb(NO₃)₂, LiCl, and SnCl₂ showed both anti-glucocorticoid and anti-mineralocorticoid activities. Comprehensive screening and evaluation of GR and MR antagonists and agonists among metals should be considered to better understand the ecological and health risks of metals.

Microcystin-LR (MC-LR) is the most abundant toxicant among microcystin variants produced by cyanobacteria. MC-induced toxicity is broadly reported to pose a threat to aquatic animals and humans and has been associated with the dysfunction of some organs such as liver and kidney. However, MC-induced neurotoxicity has not been well characterized after long-term exposure. This study was designed to investigate the neurotoxic effects after chronic oral administration of MC-LR. In our trial, C57/BL6 mice received MC-LR at 0, 1, 5, 10, 20 and 40 μg/L in drinking water for twelve months. Our data demonstrated that mitochondrial DNA (mtDNA) damage was evident in the damaged neurons as a result of chronic exposure. Histopathological abnormalities and mtDNA damage were observed in the hippocampus and cerebral cortex. Furthermore, MC-LR exerted distinct effects on these two brain regions. The hippocampus was more susceptible to the treatment of MC-LR compared with the cerebral cortex. However, no strong relationships were observed between the genotoxic effects and exposure doses. In conclusion, this study has provided a mtDNA-related mechanism for underlying chronic neurotoxicity of MC-LR and suggested the presence of differential toxicant effects on the hippocampus and cerebral cortex.

The mutual influences of C₆₀ fullerene (C₆₀) and heavy metal ions (Cd, Cu, and Pb) on the uptake, transportation, and accumulation of these coexisting pollutants in four rice cultivars planted in agricultural soil were investigated during the whole life cycle of rice. The biomass of the rice plants was not affected significantly by the presence of C₆₀. C₆₀ exposure exerted different impacts on the bioaccumulation of Cd, Cu, and Pb in various rice tissues. For example, the bioaccumulation of Cd in rice 9311 panicles was significantly decreased (p < .05) when it was exposed to 1000 mg/kg C₆₀, whereas the changes of Cu and Pb levels in panicles were not statistically significant. C₆₀ was absorbed by rice roots and transported to the stems and panicles, and it tended to form aggregates in rice tissues. C₆₀ concentrations in the roots, stems, and panicles of the four rice cultivars that were harvested after a 130-day exposure to 600 mg/kg C₆₀ were 40–292, 4.4–24.5 and 0.077–1.2 mg/kg (dry weight), respectively. C₆₀ and heavy metal ions exhibited different uptake and transportation mechanisms, which depended on the rice cultivar, soil heavy metal ion concentration, and C₆₀ exposure time and concentration. For example, the average C₆₀ in the four rice cultivars was increased sharply, from 47.4 to 196.3 mg/kg from the tillering to booting stages, whereas Cd levels increased only slightly, from 23.1 to 25.9 mg/kg. The study demonstrated that the bioaccumulation of C₆₀ and heavy metal ions under co-contamination scenario differs from under single contaminant. The accumulation of C₆₀ in rice panicles may increase the concern of food safety.