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Abstract Urban residents spend the majority of time in indoor environments, which, however, may not be a safe haven for staying away from outdoor air pollution, especially in China. To examine this hypothesis, the particle mass concentrations (0.056–18 μm) and number concentrations (14–660 nm) were simultaneously measured in and outside of three typical urban indoor settings (n = 9), i.e., school, office and residence in Guangzhou, China from October–November 2014 (dry weather season) and June–August 2015 (wet weather season). The indoor and outdoor particle number concentrations were positively correlated with each other at all three sampling settings for both dry and wet weather seasons (r 2 = 0.13–0.65, p < 0.001). The infiltration factors and indoor/outdoor ratios of particles (14–660 nm) were estimated at 0.30–0.75 and 0.85–1.5, respectively, which were comparable to or higher than those (0.12–0.76 and 0.03–1.1) found in cites of other countries under infiltration conditions. Furthermore, the average infiltration factor of fine particle numbers (50–660 nm) in an office was 0.61 during a severe haze episode, indicating that approximately 60% of outdoor particles penetrated indoors. All findings suggested an efficient transport of outdoor particle sources into indoor environment, confirming that exposure of the general public to indoor particles in China should not be overlooked due to effective infiltration of outdoor particles and frequent heavy haze episodes. Graphical abstract Image 1 Highlights • Indoor and outdoor particle number concentrations were significantly correlated. • Particle infiltration factors in Guangzhou were greater than those in other cities. • Indoor microenvironments with great infiltration of outdoor particles is not safe. [ABSTRACT FROM AUTHOR]

Human and ecological risks of BDE-209 have drawn much attention, particularly with growing e-waste recycling activities in developing countries. To further address the issue of BDE-209 biotransformation, a laboratory-controlled study was conducted. Female Sprague-Dawley rats were dosed orally by gavage at a daily dose of 1 mg kg −1 body weight for 7 d and a depuration period of 22 d, to characterize absorption, distribution, metabolism, and elimination dynamics of BDE-209 during multi-dose exposures simulating short-term oral exposure of e-waste workers. The concentrations of BDE-209 in all tissues increased exponentially during the 7-d exposure period, indicating that multi-dose exposure could lead to increased accumulation of BDE-209 in rats. The liver accumulated the greatest amount of BDE-209 on a wet-weight basis, while adipose tissue had the highest concentration by the end of the 22-d depuration period. Half-lives of BDE-209, 207, and 197 during depuration were 1.1 ± 0.1, 2.7 ± 0.3, and 10.5 ± 3.1 d in serum and 0.9 ± 0.1, 2.2 ± 0.2, and 11.8 ± 2.3 d in liver, i.e., the half-life increased with decreasing level of bromination from deca- to octa-BDEs and was similar in both serum and liver. By contrast, the half-life of the debromination metabolite BDE-207 (21.7 ± 7.7 d) was longer in small intestine than in serum and liver, suggesting slower depletion of BDE-209 metabolites in small intestine. The metabolism of BDE-209 was not responsible for the occurrence of low brominated BDE congeners and OH and MeO-PBDEs in human tissues. [ABSTRACT FROM AUTHOR]

Abstract: Rainwater samples were simultaneously collected from three locations in Guangzhou, a mega metropolitan center in South China, during the entire year of 2010, and analyzed for particulate matter (PM), total organic carbon and polycyclic aromatic hydrocarbons (PAHs), with the objectives of assessing the seasonality of washout effects and efficiency for removal of pollutants from the atmosphere by wet deposition. The contents of PM, particulate organic carbon, and dissolved organic carbon were in the ranges of 0.74–420 (average: 8.1 mg L−1), 0.16–40 (average: 1.3 mg L−1), and 0.34–6.9 mg L−1 (average: 1.4 mg L−1), respectively. Concentrations of Σ15PAH (sum of the 16 priority PAH compounds defined by the United States Environmental Protection Agency minus naphthalene) in wet deposition samples ranged from 39 to 1580 ng L−1 with an average of 170 ng L−1. The PAH concentration levels were slightly abated compared to those acquired previously in Guangzhou during the year of 2005, probably indicating a favorable change of energy consumption patterns in the region. There were moderately significant negative correlations between washout ratios and rainfall intensities (0–4.3 mm h−1). The total annual fluxes of wet and dry depositions combined for PM and PAHs in the urban area of Guangzhou were 34 g m−2 yr−1 and 6.0 × 102 μg m−2 yr−1 with 50 and 57% being contributed from wet deposition, respectively. The monthly capacity for removal (CR) of PM and PAHs (calculated as the wet deposition flux dividing the total flux) varied widely with different months, and was lower during the dry weather season (January–March and October–December) than during the wet weather season (April–September). Finally, the air quality index related to PM10 was negatively correlated to CR values of PM and PAHs, indicating the need to control the emissions of anthropogenically derived pollutants during the dry weather season. [Copyright &y& Elsevier]

Biomass fuels remain main energy sources in many remote rural regions, but potential health hazards from exposure to biomass combustion fumes have not been adequately assessed. Combustion of biomass fuels generates abundant polycyclic aromatic hydrocarbons (PAHs); hence residential exposure to PAHs can be used to evaluate the potential health risk to remote rural populations. The present study selected rural Tibetans to address the above-mentioned issue. Samples of indoor air and dust, human urine and local foods (Tsampa flour and buttered tea) were collected from five rural households in Langkazi County, an agricultural and pasturing region in Tibet of China in the summer season, which represented the best-case scenario as no heating was required. Residential exposure to PAHs by adults amounted to benzo[ a ]pyrene equivalent (BaP eq ) dosages of 110–760, 1.2–50 and 0.5–23 ng d −1 for ingestion, inhalation and dermal contact, respectively. Daily intakes of naphthalene, fluorene, phenanthrene and pyrene estimated from urinary monohydroxy PAH metabolites and from diet and inhalation exposure to PAHs were comparable (3.9, 1.9, 12 and 3.3 μg d −1 versus 9.5, 2.5, 5.1 and 1.1 μg d −1 ), indicating the utility of external exposure in assessing daily intake of PAHs. The median incremental lifetime cancer risk was 32 × 10 −6 (95% confidence interval: 0.7–73 × 10 −6 ) for ingestion and 2.4 × 10 −6 (95% confidence interval: 0.02–12 × 10 −6 ) for inhalation and dermal contact combined, indicating moderate to slight potential cancer risk. Diet is the dominant source of health hazards for rural Tibetans, but cooking fumes also present a meaningful concern. The present study demonstrates that the pristine lifestyles of remote rural residents may be of global health concern, and merit further investigations. [ABSTRACT FROM AUTHOR]

[Display omitted] • Particles release from erasers and pen grips upon dermal contact. • Particles derived from erasers and pen grips are mainly smaller than 1 μm. • Migrated particles mediate dermal contact of plasticizers to erasers and pen grips. Dermal exposure to chemicals released from daily consumer products is a rising concern, particularly for children who are susceptible to unintentional hand-to-mouth transfer and related chemical exposure risk. However, chemical transfer induced by tiny particles of intact products has yet to be adequately addressed. The objective of the present study was to determine the potentiality of particles release from intact erasers and pen grips upon dermal contact by measuring the migration rates of the embedded plasticizers (phthalates and its alternatives). The results showed that billions of particles were released from erasers (0.6–1.2 × 109) and pen grips (0.2–1.6 × 108) upon dermal contact at ambient temperature, with sizes mainly smaller than 1 μm. The composition of eraser leachates was identical to that of the corresponding bulk eraser, as confirmed by Fourier-transform infrared spectroscopy and pyrolysis. Migrated hydrophobic plasticizers may be used as indicators of particle release from erasers and pen grips. The potentiality of particle release was negatively correlated with the total plasticizer contents (r = −0.51; p < 0.05) for both erasers and pen grips. These findings indicated that particles directly released from school supplies and accessories could be a non-negligible source of human exposure to plasticizers. [ABSTRACT FROM AUTHOR]

Abstract Bioaccessibility of particle-bound hydrophobic organic contaminants and related particle size effects are significant for assessing the potential human health risk via inhalation exposure, but have not been clearly evaluated. To fill this knowledge gap, the present study developed an in vitro method to estimate the inhalation bioaccessibility of particulate polycyclic aromatic hydrocarbons (PAHs) using simulated human lung fluids, i.e. , a modified Gamble's solution (MGS) and artificial lysosomal fluid (ALF) with Tenax as the absorption media. Assay parameters, namely incubation time (10 d) and influence of filter use, were optimized for establishing the in vitro method. The results showed that the bioaccessibility of PAHs increased with increasing particle size, but other factors, such as total organic carbon and chemical hydrophobicity, also played a large role in the fate of these compounds. The results from this portion of the present study were then used to evaluate human health risk, which showed that the risk of these particle-bound PAHs by incorporating size-dependent PAHs bioaccessibility and deposition efficiency in the human respiratory tract into inhalation exposure risk calculations was reduced by >90% when compared to using total concentration. This suggested that the inhalation bioaccessibility and deposition efficiency of hydrophobic organic chemicals should be included in human health risk assessment. Graphical abstract Unlabelled Image Highlights • An in vitro method was developed for evaluating the IBAF of particle-bound HOCs. • The inhalation bioaccessibility of PAHs decreased with increasing hydrophobicity. • The IBAF of particle-bound HOCs is significant to human health risk assessment. [ABSTRACT FROM AUTHOR]

Cultivation of microalgae in anaerobically digested effluent is beneficial for removal of nutrients, such as nitrogen and phosphorus, and heavy metals at reduced cost and generation of biomass to produce biofuels. In the present study, four strains of oleaginous microalgae, separated from fresh water in South China, were evaluated for their ability to remove nitrogen and phosphorus. The results showed that Scenedesmus sp. (GN 171) was capable of removing nitrogen and phosphorous in BG-11 medium at the rates of 97% and 99%. Two types of anaerobically digested effluents, i.e., grass anaerobically digested effluent and molasses wastewater anaerobically digested effluent, were chosen as the nutrient sources. These anaerobically digested effluents diluted in BG-11 medium or with tap water were used as the substitute medium to cultivate GN 171; other pretreatment methods, such as sterilization and dilution ratio, were also taken into consideration. A ratio of 1/3 for unsterilized grass anaerobically digested effluent/tap water mixture (designated as G4) was the optimal proportion for growth of GN 171 and removal of nitrogen and phosphorus at a large scale. The dry weight of GN 171 reached 3.2 g L −1 , and the total lipid, carbohydrate and protein contents were 34%, 30% and 16% in G4. The efficacies for removal of total nitrogen, ammonia nitrogen, phosphorus and selected heavy metals were generally satisfactory. It seems possible to use ADE, rather than any artificial medium, as the sole nutrient source for microalgae production. [ABSTRACT FROM AUTHOR]

The partition coefficient (K pew) of an analyte between low-density polyethylene (LDPE) film and water is a critical parameter for measuring freely dissolved concentrations of the analyte with PE passive sampling devices. Measuring log K pew for super hydrophobic organic chemicals (HOCs) have been proven extremely difficult. The present study developed a large volume model for measuring log K pew of super HOCs, i.e., novel halogenated flame retardants (NHFRs). Results showed that the measured log K pew values of selected PAHs and PCBs obtained by the large volume model were in line with those from the co-solvent model and the literature data within less 0.3 log units of difference, while those of NHFRs (6.27–7.34) except for hexachlorocyclopentadienyldibromocyclooctane (HCDBCO) and Decabromodiphenyl ethane (DBDPE) were significantly lower than those (6.51–8.89) from the co-solvent model. A curvilinear relationship was observed between log K pew and log K ow of all target compounds, with the turning point at log K ow = ∼8.0 in the large volume model, but that was not found for the co-solvent model. These can be attributed to the large molecular volumes (> 450 Å3) for NHFRs, which require high Gibbs free energy to penetrate into the inside structures of LDPE in the large volume model. However, the solvent swelling effects in the co-solvent model needs to be investigated. Therefore, the large volume model is robust to determine the K pew values of super HOCs for facilitating the application of aquatic passive sampling techniques. • The large volume model is feasible to measure the K pew values of super HOCs. • The K pew values of HOCs from the co-solvent model were greater than other models. • The K pew values of NHFRs decreased with increasing molecular volumes. [ABSTRACT FROM AUTHOR]

Passive sampling techniques have been widely used to determine the dissolved concentration profiles of hydrophobic organic compounds (HOCs) in sediment porewater. However, the effects of having a protection for the passive sampler on profiling HOCs concentrations in sediment porewater, especially in deep sediment, have remained unclear. To address this issue, low density polyethylene passive samplers with and without protectors, which consisted of glass fiber filter and porous stainless steel shield, were simultaneously deployed in sediment of the Dongjiang River, South China. The results showed that the protectors retarded the dissipation of performance reference compounds (PRCs) from the sampler by a factor of 2–9. The protectors seemed to exert a negligible effect on the measured concentrations of PAHs, BDE-47, and BDE-99 in surficial sediment porewater (0–14 cm depth) from both samplers. However, the sediment porewater concentration profiles of PAHs and BDE-47 from the sampler with protectors were in agreement with those normalized by dry weight in deep sediment (16–34 cm depth), indicating that a diffusion layer established by the protectors may minimize the probability of local depletion of the target analytes in deep sediment. In addition, the log K oc values of PAHs, BDE-47, and BDE-99 exhibited a slight increasing trend with sediment depth. This finding suggested that in situ passive sampling techniques could be a feasible tool in determining the site-specific log K oc values of HOCs at different sediment depths. Image 1 • Protectors significantly retarded the dissipation of PRCs. • Protectors did not affect the measured concentrations of PAHs in surficial porewater. • PAHs profile from the sampler with protectors was similar to that in deep sediment. [ABSTRACT FROM AUTHOR]