Mixture Risk Drivers in Freshwater Sediments and Their Bioavailability Determined Using Passive Equilibrium Sampling.

The identification of mixture risk drivers is a great challenge for sediment assessment, especially when taking bioavailability into consideration. The bioavailable portion, which comprises the organic contaminants in pore water and the ones bound to organic carbon, was accessed by equilibrium partitioning to polydimethylsiloxane (PDMS). The exhaustive solvent and PDMS extracts were toxicologically characterized with a battery of in vitro reporter gene assays and chemically analyzed with liquid and gas chromatography coupled to high-resolution mass spectrometry. The bioavailable fractions of mixture effects and individual chemicals were mostly lower than 0.1, indicating that more than 90% of the substances are strongly bound and would not pose an immediate risk but could potentially be remobilized in the long term. Despite 655 organic chemicals analyzed, only 0.1-28% of the observed biological effects was explained by the detected compounds in whole sediments, while 0.009-3.3% was explained by bioavailable chemicals. The mixture effects were not only dominated by legacy pollutants (e.g., polycyclic aromatic hydrocarbons (PAHs) in the bioassay for activation of the aryl-hydrocarbon receptor (AhR) and oxidative stress response (AREc32)) but also by present-use chemicals (e.g., plastic additives for binding to the peroxisome proliferator-activated receptor γ (PPARγ)), with different fingerprints between whole sediments and bioavailable extracts. Our results highlight the necessity to involve different bioassays with diverse effect profiles and broader selection of contaminants along with bioavailability for the risk assessment of chemical mixtures in sediments.

Seasonal source analysis of nitrogen and carbon aerosols of PM2.5 in typical cities of Zhejiang, China.

Fine particulate matter (PM2.5) significantly impacts global air quality and human health due to its smaller particle size and larger specific surface area. Nitrogen and carbon aerosols, as the main components of PM2.5, play key roles in air pollution. This study identified the sources and seasonal variation of nitrogen and carbon aerosols in PM2.5 in typical cities of Zhejiang. The annual average PM2.5 concentrations of Hangzhou (HZ), Ningbo (NB), and Huzhou (HUZ) were 39.8 ± 19.1 µg m-|3, 40.0 ± 21.5 µg m-3, and 50.1 ± 22.6 µg m-3, respectively, which exceeded the Chinese air quality limit of 35.0 µg m-3. The results showed that the concentrations of nitrogen aerosols (NO3- and NH4+) in water-soluble inorganic ions were higher at 9.6 ± 4.6 µg m-3, 9.0 ± 4.5 µg m-3 and 11.5 ± 5.4 µg m-3 in HZ, NB and HUZ, respectively, especially in winter, accounting for over 60% of the total. The annual average δ15N values of PM2.5 were 6.2 ± 1.9‰, 6.4 ± 2.2‰ and 6.7 ± 1.9‰ in HZ, NB and HZ, respectively; the δ15N values in winter were relatively low. A Bayesian isotopic mixing model was employed to analyse the sources of nitrogen aerosols in winter; the results showed that nitrogen concentration was mainly affected by NH3 and NOX emitted by motor vehicle exhaust, coal combustion, biomass combustion, biogenic soil emissions, animal wastes and ocean evaporation (NB). In addition, the carbon component analysis of PM2.5 showed that the annual average mass concentration of TC accounted for 18.7%, 16.4% and 20.1% of PM2.5 in HZ, HUZ and NB, respectively. The same isotope model was used to analyse the sources of carbon aerosols; the results showed that carbon aerosols were mainly affected by the sources of motor vehicle exhaust, coal combustion, biomass combustion and dust. In the PM2.5 in Zhejiang, the most contributory sources of nitrogenous aerosols and carbon aerosols were motor vehicle exhaust sources.

Congener-specific composition of polychlorinated biphenyls (PCBs) in soil-air partitioning and the associated health risks.

The recent changes in the compositions of polychlorinated biphenyls (PCBs) after their restriction for 40 years may have various effects on human health. In order to characterize the congener-specific compositions of PCBs in the soil-air process and assess the associated human health risks, soil and air samples were simultaneously collected in winter and summer at two different functional locations. Homologue patterns suggest that long-range atmospheric transport might be the major source of soil and air residues of PCBs. The net deposition from air to soil was overwhelming for most PCB congeners. Variations in the occurrence and the homologue patterns of PCBs between the soil and air interface depended on chemical volatility, soil organic matter (OM) content, ambient temperature, topographical condition and atmospheric transport. Dioxin-like PCBs accounted for 11.0-70.3% and 2.31-54.8% of total PCB residues in soil and air, respectively. Non-carcinogenic and carcinogenic risks associated with exposure to soil and air PCBs were also estimated. Different PCB congeners showed different health effects, with the highest contribution from PCB-26. Additionally, the non-carcinogenic risk levels of PCBs were enhanced, while the carcinogenic risk levels decreased during the soil-air exchange process of PCBs with time. Our results highlight the soil-air interaction of PCBs in predicting their potential human exposure health risks.