Whereas air pollution in many Chinese cities has reached epidemic levels in recent years, limited research has explored the spatial and temporal patterns of fine air particles such as PM2.5, or particulate matter with diameter smaller than 2.5 μm, using nationally representative data. This article applied spatial statistical approaches including spatial interpolation and spatial regression to the analysis of ground-level PM2.5 observations for 190 Chinese cities in 2014 obtained from the Chinese Air Quality Online Monitoring Platform. Results of this article suggest that most Chinese cities included in the dataset recorded severe levels of PM2.5 in excess of the WHO’s interim target and cities in the North China Plain had the highest levels of PM2.5 regardless of city size. Spatially interpolated maps of PM2.5 and population-weighted PM2.5 indicate vast majority of China’s land and population was exposed to disastrous levels of PM2.5 concentrations. The regression results suggest that PM2.5 in a city was positively related to its population size, amount of atmospheric pollutants, and emissions from nearby cities, but inversely related to precipitation and wind speed. Findings from this research can shed new light on the complex spatiotemporal patterns of PM2.5 throughout China and provide insights into policies aiming to mitigate air pollution in China.

This study applies remote sensing technology to assess and examine the spatial and temporal Brightness Temperature (BT) profile in the city of Tel-Aviv, Israel over the last 30 years using Landsat imagery. The location of warmest and coldest zones are constant over the studied period. Distinct diurnal and temporal BT behavior divide the city into four different segments. As an example of future application, we applied mixed regression models with daily random slopes to correlate Landsat BT data with monitored air temperature (Tair) measurements using 14 images for 1989–2014. Our preliminary results show a good model performance with R² = 0.81. Furthermore, based on the model's results, we analyzed the spatial profile of Tair within the study domain for representative days.

A pot experiment was conducted to investigate the effects of biochars on the availability of heavy metals (Cd, Cu, Mn, Ni, Pb, and Zn) to ryegrass in an alkaline contaminated soil. Biochars only slightly decreased or even increased the availability of heavy metals assesses by chemical extractant (a mixture of 0.05 mol L−1 ethylenediaminetetraacetic acid disodium, 0.01 mol L−1 CaCl2, and 0.1 mol L−1 triethanolamine). The significantly positive correlation between most chemical-extractable heavy metals and the ash content in biochars indicated the positive role of ash in this extraction. Biochars significantly reduced the plant uptake of heavy metals, excluding Mn. The absence of a positive correlation between the chemical-extractable heavy metals and the plant uptake counterparts (except for Mn) indicates that chemical extractability is probably not a reliable indicator to predict the phytoavailability of most heavy metals in alkaline soils treated with biochars. The obviously negative correlation between the plant uptake of heavy metals (except for Mn) and the (O + N)/C and H/C indicates that biochars with more polar groups, which were produced at lower temperatures, had higher efficiency for reducing the phytoavailability of heavy metals. The significantly negative correlations between the plant uptake of Mn and ryegrass biomass indicated the “dilution effect” caused by the improvement of biomass. These observations will be helpful for designing biochars as soil amendments to reduce the availability of heavy metals to plants in soils, especially in alkaline soils.

There is mounting evidence indicating that microcystins (MCs) are heptapeptide toxins. Recent studies have also shown that MCLR can transfer from mother to offspring, but it is unclear whether maternal MCLR can influence the liver of offspring or not. In this study, pregnant SD rats were injected intraperitoneally with a saline solution (control) or 10 μg/kg MCLR per day from gestational day 8 (GD8) to postnatal day 15 (PD15) for a total of 4 weeks. 2-DE and MALDI-TOF-TOF mass spectrometry were used to screen for MCLR target proteins in the livers of rat pups. Our results demonstrated that MCLR could accumulate in the livers of neonatal rats. Proteomics studies also showed that MCLR significantly influenced many proteins, including those involved in the cytoskeleton, metabolism and particularly oxidative stress. In addition, MCLR induced cellular structural damage and resulted in the production of intracellular reactive oxygen species (ROS) and lipid peroxidation. Moreover, protein phosphatase (PP) activity was inhibited and some serum biochemistry parameters were altered. These results suggest an early molecular mechanism behind the hepatotoxicity induced by maternal MC exposure and highlight the importance of monitoring MC concentrations in new-born mammals.

The presence of polycyclic aromatic hydrocarbons (PAHs) in biochars hinders their environmental use. The aim of this study was to determine the freely dissolved (Cfree) PAH content in soil amended with biochar in a long-term (851 days) field experiment. Biochar was added to the soil at a rate of 30 and 45 t/ha. The addition of biochar to the soil resulted in a decrease in Σ13 Cfree PAHs by 25 and 22%, in the soil with the addition of biochar at the rate of 30 and 45 t/ha, respectively. As far as individual PAHs are concerned, in most cases a reduction in Cfree was also observed (from 3.6 to 66%, depending on the biochar rate). During the first 105 days of the experiment, the content of Σ13 Cfree in the biochar-amended soil significantly decreased by 26% (30 t/ha) and 36% (45 t/ha). After this period of time until the end of the experiment, no significant changes in Cfree were observed, regardless of the biochar rate. However, the behavior of individual PAH groups differed depending on the number of rings and experimental treatment. Ultimately, after 851 days of the experiment the content of Σ13 Cfree PAHs was lower by 29% (30 t/ha) and 35% (45 t/ha) compared to the beginning of the study as well as lower by 40% (30 t/ha) and 42% (45 t/ha) than in the control soil. The log KTOC coefficients calculated for the biochar-amended soils were higher immediately after adding biochar and subsequently they gradually decreased, indicating the reduced strength of the interaction between biochar and the studied PAHs. The obtained results show that the addition of biochar to soil does not create a risk in terms of the content of Cfree PAHs.

Measurement of atmospheric mercury speciation was conducted in a coastal city of the Yangtze River Delta, China from July 2013 to January 2014, in conjunction with air pollutants and meteorological parameters. The mean concentrations of gaseous elemental mercury (GEM), particulate bound mercury (HgP) and reactive gaseous mercury (RGM) were 3.26 ± 1.63 ng m−3, 659 ± 931 pg m−3, and 197 ± 246 pg m−3, respectively. High percentages of HgP during haze days were found, due to the increase in direct emissions and gas-particle partitioning of RGM. The average gas-particle partitioning coefficients (Kp) during moderate or severe haze days (PM2.5 > 150 μg m−3) were obviously decreased. GEM and HgP were positively correlated with PM2.5, SO2, NO2 and CO, suggesting a significant contribution of anthropogenic sources. Elevated HgP concentrations in cold seasons and in the morning were observed while RGM exhibited different seasonal and diurnal pattern. The ratio of HgP/SO2 and Pearson correlation analysis suggested that coal combustion was the main cause of increasing atmospheric Hg concentrations. The monitoring site was affected by local, regional and interregional sources. The back trajectory analysis suggested that air mass from northwest China and Huabei Plain contributed to elevated atmospheric Hg in winter and autumn, while southeast China with clean air masses were the major contributor in summer.

In the situation of increasing agricultural utilization of residues from biogas production (RBP) it is important to determine the concentration of contaminants, which could occur in these materials. The group of contaminants that requires special attention are polycyclic aromatic hydrocarbons (PAH). The objective of the study was to determine the total and freely dissolved (Cfree) of PAHs in RBP from 6 different biogas plants operating under various temperature conditions and without or with the separation into the solid and liquid fractions. The freely dissolved PAHs were determined using polyoxymethylene (POM method). The total content of the Σ16 PAHs in RBP varied from 449 to 6147 μg/kgdw, while that of Cfree PAHs was at the level from 57 to 653 ng/L. No significant differences were noted in the content of the Σ16 PAHs (total) between the solid and the liquid fractions. This indicates that in the course of the separation, the PAHs are distributed proportionally between the fractions. However in the case of Cfree, PAHs content in the solid fraction was over twice as high as in the liquid fraction. This was probably due to the greater affinity of the particles present in the liquid fraction to the analysed PAHs than to the particles of the solid fraction. Higher affinity to liquid fraction was also confirmed by the distribution coefficients KTOC determined on the basis of Cfree.

We observed PM2.5, PM10 concentration, aerosol optical depth (AOD), and Ångström exponents (α) in three typical stations, the Beijing city, the Xianghe suburban and the Xinglong background station in the Beijing metropolitan region, from 2009 to 2010, synchronously. The annual means of PM2.5 (PM10) were 62 ± 45 (130 ± 88) μg m−3 and 79 ± 61 (142 ± 96) μg m−3 in the city and suburban region, which were much higher than the regional background (PM2.5: 36 ± 29 μg m−3). The annual means of AOD were 0.53 ± 0.47 and 0.54 ± 0.46 and 0.24 ± 0.22 in the city, suburban and the background region, respectively. The annual means of Ångström exponents were 1.11 ± 0.31, 1.09 ± 0.31 and 1.02 ± 0.31 in three typical stations. Meanwhile, the rates of PM2.5 accounting for PM10 were 44%–54% and 46%–70% in the city and suburban region during four seasons. The pollution of fine particulate was more serious in winter than other seasons. The linear regression functions of PM2.5 (y) and ground-observed AOD (x) were similarly with high correlation coefficient in the three typical areas, which were y = 74x + 18 (R2 = 0.58, N = 337, in the City), y = 80x + 25 (R2 = 0.55, N = 306, in the suburban) and y = 87x + 9 (R2 = 0.64, N = 350, in the background). The functions of PM10 (y) and ground-observed AOD (x) were y = 112x + 57 (R2 = 0.54, N = 337, in the city) and y = 114x + 68 (R2 = 0.47, N = 304, in the suburban). But the functions had large differences in four seasons. The correlations between PM2.5, PM10 and MODIS AOD were similar with the correlations between PM2.5, PM10 and the ground-observed AOD. With MODIS C6 AOD, the distributions of PM2.5 and PM10 concentration were retrieved by the seasonal functions. The absolute retrieval errors of seasonal PM2.5 distribution were less than 5 μg m−3 in the pollutant city and suburb, and less than 7 μg m−3 in the clean background.

Stable Pb isotope ratios (Pb-IRs) have been recognized as an efficient tool for identifying sources. This study carried out at Kabwe mining area, Zambia, to elucidate the presence or absence of Pb isotope fractionation in goat and chicken, to evaluate the reliability of identifying Pb pollution sources via analysis of Pb-IRs, and to assess whether a threshold for blood Pb levels (Pb-B) for biological fractionation was present. The variation of Pb-IRs in goat decreased with an increase in Pb-B and were fixed at certain values close to those of the dominant source of Pb exposure at Pb-B > 5 μg/dL. However, chickens did not show a clear relationship for Pb-IRs against Pb-B, or a fractionation threshold. Given these, the biological fractionation of Pb isotopes should not occur in chickens but in goats, and the threshold for triggering biological fractionation is at around 5 μg/dL of Pb-B in goats.

Over recent decades, efforts have been made to reduce human exposure to atmospheric pollutants including polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs) through emission control and abatement. Along with the potential changes in their concentrations resulting from these efforts, profiles of emission sources may have also changed over such extended timeframes. However relevant data are quite limited in the Southern Hemisphere. We revisited two sampling sites in an Australian city, where the concentration data in 1994/5 for atmospheric PAHs and PCBs were available. Monthly air samples from July 2013 to June 2014 at the two sites were collected and analysed for these compounds, using similar protocols to the original study. A prominent seasonal pattern was observed for PAHs with elevated concentrations in cooler months whereas PCB levels showed little seasonal variation. Compared to two decades ago, atmospheric concentrations of ∑13 PAHs (gaseous + particle-associated) in this city have decreased by approximately one order of magnitude and the apparent halving time (t1/2) was estimated as 6.2 ± 0.56 years. ∑6iPCBs concentrations (median value; gaseous + particle-associated) have decreased by 80% with an estimated t1/2 of 11 ± 2.9 years. These trends and values are similar to those reported for comparable sites in the Northern Hemisphere. To characterise emission source profiles, samples were also collected from a bushfire event and within a vehicular tunnel. Emissions from bushfires are suggested to be an important contributor to the current atmospheric concentrations of PAHs in this city. This contribution is more important in cooler months, i.e. June, July and August, and its importance may have increased over the last two decades.