Numerous studies have evaluated the effects of long-term exposure to ambient air pollution on hypertension. However, little information exists regarding its effects on prehypertension, a very common, but understudied cardiovascular indicator. We evaluated data from 24,845 adults (ages 18–74 years) living in three Northeastern Chinese cities in 2009. Blood pressure (BP) was measured by trained observers using a standardized mercuric-column sphygmomanometer. Three-year (from 2006 to 2008) average concentrations of particles with an aerodynamic diameter ≤10 μm (PM10), sulfur dioxide (SO2), nitrogen dioxides (NO2), and ozone (O3) were calculated using data from monitoring stations. Effects were analyzed using generalized additive models and two-level regression analyses, controlling for covariates. We found positive associations of all pollutants with prehypertension (e.g. odds ratio (OR) was 1.17 (95% confidence interval (CI), 1.09–1.25) per interquartile range (IQR) of PM10) in a fully adjusted model, as compared to normotensive participants. These associations were stronger than associations with hypertension (e.g. OR was 1.03 (95% CI, 1.00, 1.07) per IQR of PM10). We have also found positive associations of all studied pollutants with systolic and diastolic BP: e.g., associations with PM10 per IQR were 1.24 mmHg (95% CI, 1.03–1.45) for systolic BP and 0.47 mmHg (95% CI, 0.33–0.61) for diastolic BP. Further, we observed that associations with BP were stronger in women and in older participants (systolic BP only). In conclusion, long-term exposure to ambient air pollution was more strongly associated with prehypertension than with hypertension, especially among females and the elderly. Thus, interventions to reduce air pollution are of great significance for preventing future cardiovascular events, particularly among individuals with prehypertension.

An on-line source-tagged model coupled with an air quality model (Nested Air Quality Prediction Model System, NAQPMS) was applied to estimate source contributions of primary and secondary sulfate, nitrate and ammonium (SNA) during a representative winter period in Shanghai. This source-tagged model system could simultaneously track spatial and temporal sources of SNA, which were apportioned to their respective primary precursors in a simulation run. The results indicate that in the study period, local emissions in Shanghai accounted for over 20% of SNA contributions and that Jiangsu and Shandong were the two major non-local sources. In particular, non-local emissions had higher contributions during recorded pollution periods. This suggests that the transportation of pollutants plays a key role in air pollution in Shanghai. The temporal contributions show that the emissions from the “current day” (emission contribution from the current day during which the model was simulating) contributed 60%–70% of the sulfate and ammonium concentrations but only 10%–20% of the nitrate concentration, while the previous days’ contributions increased during the recorded pollution periods. Emissions that were released within three days contributed over 85% averagely for SNA in January 2013. To evaluate the source-tagged model system, the results were compared by sensitivity analysis (emission perturbation of −30%) and backward trajectory analysis. The consistency of the comparison results indicated that the source-tagged model system can track sources of SNA with reasonable accuracy.

High energy electron-impact ionizers have found applications mainly in industry to reduce off-gas emissions from waste gas streams at low cost and high efficiency because of their ability to oxidize many airborne organic pollutants (e.g., volatile organic compounds (VOCs)) to CO2 and H2O. Applications of air ionizers in indoor air quality management are limited due to poor removal efficiency and production of noxious side products, e.g., ozone (O3). In this paper, we provide a critical evaluation of the pollutant removal performance of air ionizing system through comprehensive review of the literature. In particular, we focus on removal of VOCs and odorants. We also discuss the generation of unwanted air ionization byproducts such as O3, NOx, and VOC oxidation intermediates that limit the use of air-ionizers in indoor air quality management.

The spatial distribution, compositional profiles, and enantiomer fractions (EFs) of organochlorine pesticides (OCPs), including hexachlorocyclohexanes (HCHs), dichlorodiphenyltrichloroethanes (DDTs), and chlordanes (CHLs), in the surface sediments in the Bering Sea, Chukchi Sea and adjacent areas were investigated. The total concentrations of DDTs, HCHs and CHLs varied from 0.64 to 3.17 ng/g dw, 0.19–0.65 ng/g dw, and 0.03–0.16 ng/g dw, respectively. No significant difference was observed between the Bering Sea and Chukchi Sea for most pollutants except for trans-CHL, ΣCHLs (sum of trans- and cis-chlordane) and p,p'-DDD. Concentration ratios (e.g., α-HCH/γ-HCH, o,p'-DDT/p,p'-DDT) indicated that the contamination in the studied areas may result from inputs from multiple sources (e.g., historical usage of technical HCHs as well as new input of dicofol). Chiral analysis showed great variation in the enantioselective degradation of OCPs, resulting in excess of (+)-enantiomer for α-HCH in thirty of the 32 detectable samples, preferential depletion of (−)-enantiomer for o,p'-DDT in nineteen of the 35 detectable samples, and nonracemic in most samples for trans- and cis-chlordane. The ecological risks of the individual OCPs as well as the mixture were assessed based on the calculation of toxic units (TUs), and the results showed the predominance of DDT and γ-HCH in the mixture toxicity of the sediment. Overall, the TUs of OCPs in sediments from both the Bering and Chukchi Seas are less than one, indicating low ecological risk potential.

Traditional tea (Camellia sinensis) and herbal tea are being consumed across the world. However, long term consumption of tea can increase the chances of fluorosis owing to the presence of fluoride (F) in teas. Therefore, it is imperative to assess the health risk associated with tea consumption. The main objectives of this study were to: 1) estimate total F in 47 popular teas, including traditional and herbal teas and F concentrations in 1% (w/v) infusion of 5 min, and 2) assess the exposure risks of F from tea consumption in children and adults. The data showed that total F was the least in herbal teas (33–102 mg/kg) and their infusions (0.06–0.69 mg/L) compared to traditional teas (296–1112 mg/kg) and their infusions (1.47–6.9 mg/L). During tea infusion, 6–96% and 18–99% of the F was released into the water from herbal and traditional teas, respectively. Ten samples of traditional teas, including five green teas had chronic daily intake (CDI) values of F > 0.05 mg/d/kg bw, the stipulated permissible limits of F intake from all sources. Although the F from teas posed no immediate health hazards with hazard quotient <1, some tea samples could potentially contribute >4 mg F/d, thereby adding to the overall F burden. Therefore, together with F from food and water sources, daily F consumptions from teas might increase its health risks to humans. So, caution should be excised when drinking teas containing high F.

Sulfur dioxide (SO2) is a major component of magmatic gas discharges. Once emitted in the atmosphere it can affect the air and land environment at different spatial and temporal scales, with harmful effects on human health and plant communities.We used a dense dataset of continuous SO2 flux and meteorological measurements collected at Vulcano over an 8-year period spanning from May 2008 to February 2016 to model air SO2 concentrations over the island. To this end, we adopted the DISGAS (DISpersion of GAS) numerical code coupled with the Diagnostic Wind Model (DWM). SO2 concentrations in air were determined for three different SO2 emission rates: a reference SO2 flux of ∼18 t/d (the median of more than 800 measurements), an enhanced SO2 flux of 40 t/d (average of all measurements plus 1 σ), and a maximum SO2 flux of 106 t/d (maximum value measured in the investigated period). Maximum SO2 concentrations in air were estimated at the crater, near the high-T fumarole field that is the source of the gas, and ranged from 2000 ppb to ∼24,000 ppb for the reference flux, from 2000 ppb to 51,000 ppb for the enhanced flux and from 5000 ppb to 136,000 ppb for the maximum flux, with peak values in limited areas at the bottom of the crater. These concentrations pose a hazard for people visiting the crater, for sensitive individuals in particular. Based on estimated SO2 concentrations in air, we also consider the phytotoxic effects of SO2 on local vegetation.

Photo-reduction of Ag+ to silver nanoparticle (AgNPs) by dissolved organic matter (DOM) is a possible source of naturally occurring AgNPs. However, how this photo-reduction process is influenced by ubiquitous metal ions is still not well understood. In addition, in previous studies, the formation of AgNPs in DOM solution was usually monitored by UV-Vis spectroscopy, and there is still lack of quantitative analysis for the formed AgNPs. In the present study, the role of Fe2+/Fe3+ at environmental concentration level on this photochemical process was investigated, and the enhanced formation of AgNPs by Fe2+/Fe3+ was probed and quantified by using UV-Vis spectroscopy, transmission electron microscopy, and liquid chromatography-inductively coupled plasma mass spectrometry. It was demonstrated that while Fe3+ can oxidize AgNPs to release Ag+, Fe2+ can reduce Ag+ into AgNPs. However, the DOM-induced reduction of Fe3+ makes iron an effective electron shuttle between DOM and Ag+, and both Fe2+ and Fe3+ enhanced AgNP formation. The impacts of environmentally relevant factors, including DOM concentration and solution pH, on this process were studied comprehensively, which showed that the catalytic role of iron was more significant at higher DOM concentration and lower pH. This iron-enhanced formation of AgNPs in photo-irradiated Ag+-DOM solution have great environmental implications on the formation of natural AgNPs and the transformation of engineered AgNPs in acidic surface water with high iron content.

Potential utilities of instrumented lightweight unmanned aerial vehicles (UAVs) to quickly characterize tropospheric ozone pollution and meteorological factors including air temperature and relative humidity at three-dimensional scales are highlighted in this study. Both vertical and horizontal variations of ozone within the 1000 m lower troposphere at a local area of 4 × 4 km² are investigated during summer and autumn times. Results from field measurements show that the UAV platform has a sufficient reliability and precision in capturing spatiotemporal variations of ozone and meteorological factors. The results also reveal that ozone vertical variation is mainly linked to the vertical distribution patterns of air temperature and the horizontal transport of air masses from other regions. In addition, significant horizontal variations of ozone are also observed at different levels. Without major exhaust sources, ozone horizontal variation has a strong correlation with the vertical convection intensity of air masses within the lower troposphere. Higher air temperatures are usually related to lower ozone horizontal variations at the localized area, whereas underlying surface diversity has a week influence. Three-dimensional ozone maps are obtained using an interpolation method based on UAV collected samples, which are capable of clearly demonstrating the diurnal evolution processes of ozone within the 1000 m lower troposphere.

Glyphosate is one of the most used herbicides in agricultural lands worldwide. Wind-eroded sediment and dust, as an environmental transport pathway of glyphosate and of its main metabolite aminomethylphosphonic acid (AMPA), can result in environmental- and human exposure far beyond the agricultural areas where it has been applied. Therefore, special attention is required to the airborne transport of glyphosate and AMPA. In this study, we investigated the behavior of glyphosate and AMPA in wind-eroded sediment by measuring their content in different size fractions (median diameters between 715 and 8 μm) of a loess soil, during a period of 28 days after glyphosate application. Granulometrical extraction was done using a wind tunnel and a Soil Fine Particle Extractor. Extractions were conducted on days 0, 3, 7, 14, 21 and 28 after glyphosate application. Results indicated that glyphosate and AMPA contents were significantly higher in the finest particle fractions (median diameters between 8 and 18 μm), and lowered significantly with the increase in particle size. However, their content remained constant when aggregates were present in the sample. Glyphosate and AMPA contents correlated positively with clay, organic matter, and silt content. The dissipation of glyphosate over time was very low, which was most probably due to the low soil moisture content of the sediment. Consequently, the formation of AMPA was also very low. The low dissipation of glyphosate in our study indicates that the risk of glyphosate transport in dry sediment to off-target areas by wind can be very high. The highest glyphosate and AMPA contents were found in the smallest soil fractions (PM10 and less), which are easily inhaled and, therefore, contribute to human exposure.

Influence of multiwalled carbon nanotubes with outer diameters > 50 nm (MW) and a surfactant sodium dodecyl benzene sulfonate (SDBS) on bioaccumulation and translocation of pyrene and 1-methylpyrene (1-CH3-pyrene) in maize seedlings in single-(F1) and bi-(F2) compound systems was investigated. Pyrene concentration in shoots was detected in all treatments in F1 and F2, ranging in 10.43–60.28 ng/g and 21.46–40.21 ng/g, respectively, and its translocation factors (TFs) ranged in 0.12–0.19 and 0.07–0.16. However, no 1-CH3-pyrene in shoots was detected from F1 and F2, indicating almost 100% suppression on its translocation from roots to shoots. SDBS at 100 mg/kg significantly enhanced pyrene bioaccumulation in roots and shoots by 43.5% and 77.4% in F1, and 21.7% in roots in F2, while showed insignificant effect on shoot concentration in F2. In contrast, SDBS at 100 mg/kg exerted no significant effect on root 1-CH3-pyrene concentration in F1 and F2. With increasing amendment level of MW from 50 to 3000 mg/kg, both pyrene and 1-CH3-pyrene concentrations in roots and shoots sharply decreased, indicating an increasing suppression on their bioaccumulation and translocation in plant. As for 3000 mg/kg MW + 100 mg/kg SDBS, root concentrations of pyrene and 1-CH3-pyrene in F1 were significantly reduced by 53.4% and 100%, while shoot concentration of pyrene was not affected, generally consistent with the trend of the corresponding bioaccumulation factors (BCFroot) and TFs. As for F2 with the same treatment, root 1-CH3-pyrene concentration declined by 68.6%, whereas pyrene bioaccumulation in roots and shoots was insignificantly affected, which were also in agreement with their BCFroot and TFs. Results of this work highlight the combined impacts of soil amendment with carbon nanotubes and surfactant on bioaccumulation and translocation of pyrene and 1-CH3-pyrene in maize seedlings in multi-pollutant exposure systems, which is important for soil pollution control and food safety assessment.