As the climate in California warms and wildfires become larger and more severe, satellite-based observational tools are frequently used for studying impact of those fires on air quality. However little objective work has been done to quantify the skill these satellite observations of smoke plumes have in predicting impacts to PM2.5 concentrations at ground level monitors, especially those monitors used to determine attainment values for air quality under the Clean Air Act. Using PM2.5 monitoring data from a suite of monitors throughout the Central California area, we found a significant, but weak relationship between satellite-observed smoke plumes and PM2.5 concentrations measured at the surface. However, when combined with an autoregressive statistical model that uses weather and seasonal factors to identify thresholds for flagging unusual events at these sites, we found that the presence of smoke plumes could reliably identify periods of wildfire influence with 95% accuracy.

Nano silver and nano zinc-oxide monthly concentrations in surface waters across Europe were modeled at ∼6 × 9 km spatial resolution. Nano-particle loadings from households to rivers were simulated considering household connectivity to sewerage, sewage treatment efficiency, the spatial distribution of sewage treatment plants, and their associated populations. These loadings were used to model temporally varying nano-particle concentrations in rivers, lakes and wetlands by considering dilution, downstream transport, water evaporation, water abstraction, and nano-particle sedimentation. Temporal variability in concentrations caused by weather variation was simulated using monthly weather data for a representative 31-year period. Modeled concentrations represent current levels of nano-particle production. Two scenarios were modeled. In the most likely scenario, half the river stretches had long-term average concentrations exceeding 0.002 ng L−1 nano silver and 1.5 ng L−1 nano zinc oxide. In 10% of the river stretches, these concentrations exceeded 0.18 ng L−1 and 150 ng L−1, respectively. Predicted concentrations were usually highest in July.

Rapid monitoring and discriminating different anthropogenic pollution is a key scientific issue. To detect the applicability and sensitivity of magnetic measurements for evaluating different industrial pollution in urban environment, characteristics of topsoil from three typical fast developing industrial cities (Jinchang, Baiyin and Jiayuguan in Gansu province, northwestern China) were studied by magnetic and geochemical analyses. The results showed that magnetic susceptibility was enhanced near industrial areas, and PSD-MD magnetite dominated the magnetic properties. Magnetic concentration parameters (χlf, SIRM, and χARM) showed different correlations with heavy metals and PLI in the three cities, indicating significantly different magnetic response to different pollution sources. Principal component analysis showed that ferrimagnetic minerals coexist with heavy metals of Fe, As, Cu, Pb, and Zn in Baiyin and Fe, V, Cu, Mn, Pb, and Cr in Jiayuguan. Fuzzy cluster analysis and regression analysis further indicated that the sensitivity of magnetic monitoring to fuel dust is higher than that to mineral dust near non-ferrous metal smelters, and fossil fuel consumption is an important factor for increasing magnetite content. In all the three cities, the sensitivity of magnetic monitoring to pollutants from steel plants is much higher than that from non-ferrous metal plants. Therefore, magnetic proxies provide a rapid means for detecting heavy metal contamination caused by multi-anthropogenic pollution sources in a large scale area, however, the sensitivity was controlled by pollution sources.

Both China and UNEP recommend replacing raw coal chunks with coal briquettes in household sector as clean coal technology (CCT), which has been confirmed by the decreased emissions of particulate matter and black carbon. However, the clean effect has never been systematically checked by other pollutants like polycyclic aromatic hydrocarbons (PAHs). In this study, 5 coals with different geological maturities were processed as both chunks and briquettes and burned in 3 typical coal stoves for the measurement of emission factors (EFs) of particle-bound PAHs. It was found that the EFs of 16 parent PAHs, 26 nitrated PAHs, 6 oxygenated PAHs, and 8 alkylated PAHs for coal briquettes were 6.90 ± 7.89, 0.04 ± 0.03, 0.65 ± 0.40, and 72.78 ± 18.23 mg/kg, respectively, which were approximately 3.1, 3.7, 1.9, and 171 times those for coal chunks, respectively. Such significant increases in PAH emissions increased human health risk and challenged the policy of CCT.

Accurate measurements of wet mercury (Hg) deposition are critically important for the assessment of ecological responses to pollutant loading. The Hg in wet deposition was measured over a 3-year period in the southeastern Tibetan Plateau. The volume-weighted mean (VWM) total Hg (HgT) concentration was somewhat lower than those reported in other regions of the Tibetan Plateau, but the VWM methyl-Hg concentration and deposition flux were among the highest globally reported values. The VWM HgT concentration was higher in non-monsoon season than in monsoon season, and wet HgT deposition was dominated by the precipitation amount rather than the scavenging of atmospheric Hg by precipitation. The dominant Hg species in precipitation was mainly in the form of dissolved Hg, which indicates the pivotal role of reactive gaseous Hg within-cloud scavenging to wet Hg deposition. Moreover, an increasing trend in precipitation Hg concentrations was synchronous with the recent economic development in South Asia.

The implications of biochar aging regarding their material properties as well as their interactions with other contaminants are not vivid. We report the role of biochar aging on sorption behavior of di-alkyl phthalates (PAEs). Biochars used in this study were produced from peanut-shell and their aging was simulated by chemical oxidation. The structural composition and morphology of the obtained biochars, before and after oxidation with HNO3/H2SO4, were analyzed by element composition, XPS, DRIFT, and SEM/EDX. Several experimental results unequivocally showed oxygen enrichment in the mixed acid treated samples compared to their precursors. Despite surface area reduction and pore destruction, increased PAEs sorption on oxidized biochar surfaces portrayed existence of strong PAEs binding sites. The adsorption of PAEs on oxidized biochar surface is a cumulative influence of hydrophobic interactions and pi–pi electron donor–acceptor interactions. Our results suggest that imminent aging of biochar upon environmental exposure may change their sorbent properties.

This study reports the occurrence and distribution of organophosphorus flame retardants and plasticizers (OPEs) in the Elbe and Rhine rivers. A special focus of this investigation concerns the potential impacts of a major flood event in 2013 on the OPE patterns and levels in the Elbe River. In this river, 6 of 13 OPEs were detected, with tris-ethyl-phosphate (TEP, 168 ± 44 ng/L), tris-1,3-dichloro-2-propyl-phosphate (TDCPP, 155 ± 14 ng/L) and tris-1-chloro-2-propyl phosphate (TCPP, 126 ± 14 ng/L) identified as the dominant compounds. Relative to previous studies, an increase in the concentrations and relative contributions of TDCPP to the total level of OPEs was observed, which was likely caused by its increased use as a replacement for the technical pentaBDE formulation. During the flood event, the concentrations of OPEs were similar to the normal situation, but the mass fluxes increased by a factor of approximately ten (∼16 kg/d normal versus ∼160 kg/d flood peak). No input hotspots were identified along the transects of the Elbe and Rhine rivers, and the mass flux of OPEs appeared to be driven by water discharge.

We investigated the occurrence and distribution of microplastics in surface water from the Three Gorges Reservoir. Nine samples were collected via trawl sampling with a 112 μmmesh net. The abundances of microplastics were from 3407.7 × 103 to 13,617.5 × 103 items per square kilometer in the main stream of the Yangtze River and from 192.5 × 103 to 11,889.7 × 103 items per square kilometer in the estuarine areas of four tributaries. The abundance of microplastics in the main stream of the Yangtze River generally increased as moving closer to the Three Gorges Dam. The microplastics are made exclusively of polyethylene (PE), polypropylene (PP), and polystyrene (PS). Together with microplastics, high abundance of coal/fly ash was also observed in the surface water samples. Comparing with previously reported data, microplastics in the TGR were approximately one to three orders of magnitudes greater, suggesting reservoirs as potential hot spot for microplastic pollution.

Most studies of metals exposure focus on the heavy metals. There are many other metals (the transition, alkali and alkaline earth metals in particular) in common use in electronics, defense industries, emitted via combustion and which are naturally present in the environment, that have received limited attention in terms of human exposure. We analysed samples of whole blood (172), urine (173) and drinking water (172) for antimony, beryllium, bismuth, cesium, gallium, rubidium, silver, strontium, thallium, thorium and vanadium using ICPMS. In general most metals concentrations were low and below the analytical limit of detection with some high concentrations observed. Few factors examined in regression models were shown to influence biological metals concentrations and explained little of the variation. Further study is required to establish the source of metals exposures at the high end of the ranges of concentrations measured and the potential for any adverse health impacts in children.

A total of 45 children's toys and jewelry were tested for total and bioaccessible metal concentrations. Total As, Cd, Sb, Cr, Ni, and Pb concentrations were 0.22–19, 0.01–139, 0.1–189, 0.06–846, 0.14–2894 and 0.08–860,000 mg kg−1. Metallic products had the highest concentrations, with 3–7 out of 13 samples exceeding the European Union safety limit for Cd, Pb, Cr, or Ni. However, assessment based on hazard index >1 and bioaccessible metal showed different trends. Under saliva mobilization or gastric ingestion, 11 out of 45 samples showed HI >1 for As, Cd, Sb, Cr, or Ni. Pb with the highest total concentration showed HI <1 for all samples while Ni showed the most hazard with HI up to 113. Our data suggest the importance of using bioaccessibility to evaluate health hazard of metals in children's toys and jewelry, and besides Pb and Cd, As, Ni, Cr, and Sb in children's products also deserve attention.