To evaluate the ozone (O3) sensitivity among peach tree (Prunus persica) cultivars widely planted in Beijing region and explore the possible eco-physiological response mechanisms, thirteen cultivars of peach seedlings were exposed to either charcoal-filtered air or elevated O3 (E-O3, non-filtered ambient air plus 60 ppb) for one growing season in open-top chambers. Leaf structure, stomatal structure, gas exchange and chlorophyll a fluorescence, photosynthetic pigments, antioxidant defense system and lipid peroxidation were measured in three replicated chambers. Results showed that E-O3 significantly reduced abaxial epidemis thickness, but no effects on the thicknesses of adaxial epidemis, palisade parenchyma and spongy parenchyma. Stomatal area, density and conductance were not significantly affected by E-O3. E-O3 significantly accelerated leaf senescence, as indicated by increased lipid peroxidation and more declines in light-saturated photosynthetic rate and pigments contents. The reduced ascorbate content (ASC) was decreased but antioxidant enzyme activity (CAT, APX and SOD) and total antioxidant capacity (TAC) were significantly increased by E-O3 among cultivars. The cultivars with visible symptoms also had more reductions in net photosynthetic rate than those without visible symptoms. Ozone sensitivity among cultivars was strongly linked to leaf mass per area (LMA), antioxidant enzymes activity e.g. SOD, APX rather than stomatal parameters (stomatal area, density and conductance) and ASC. Results could provide a theoretical basis for selecting and breeding the ozone-resistant cultivars of peach trees grown in high O3-polluted regions.

We investigated whether local-scale decontamination (removal of the litter layer, superficial soil layer, and understory) in a secondary forest contaminated by the Fukushima nuclear power plant accident reduced 137Cs contamination of the soil and litter. We also measured 137Cs concentrations in plants and in the web-building spider Nephila clavata (Nephilidae: Arachnida), as an indicator species, to examine 137Cs contamination in arthropods. One month after decontamination, the total 137Cs contamination (soil + litter) was reduced by 20% (100 kBq·m−2) relative to that in an adjacent untreated (i.e., contaminated) area, which was however not statistically significant. Four months after decontamination, 137Cs in the decontaminated area had increased to a level similar to those in the untreated area, and the air radiation dose in the decontaminated area was about 2.1 μSv·h−1, significantly higher than that in the untreated area (1.9 μSv·h−1). This may have been attributed to a torrential rain event. Although no statistically significant reduction was observed, most spiders had a lower 137Cs contamination than that before the decontamination. This implied that the decontamination may have reduced 137Cs transfer from soil via litter to N. clavata through the detrital food chains, but may not have reduced the amount of 137Cs transfer through grazing food chains because the concentration of 137Cs in living tree leaves was not reduced by the decontamination. In autumn, about 2 kBq·m−2 of 137Cs was supplied from foliage to the ground by litterfall. The results suggested that removal of the litter and superficial soil layers in a contaminated forest may be ineffective. The present study suggests that the local-scale decontamination in a secondary forest had no effect on the reduction of 137Cs contamination in the treated area.

Three novel organic vermiculites (VER) modified by amphoteric surfactants (BS, SB and PBS) with different negatively charged groups (carboxylate, sulfonate and phosphate) were demonstrated and used for removal of bisphenol A (BPA) and tetrabromobisphenol A (TBBPA). The difference in the structure and surface properties of modified vermiculites were investigated using a series of characterization methods. BS and SB surfactant mainly adsorbed on the surface and hard to intercalate into the interlayer of VER, while both adsorption and intercalation occurred in PBS modification. This difference resulted in different packing density of surfactant and hydrophobicity according to the results of contact angle, and affect the adsorption capacities ultimately. The adsorption of two pollutants onto these modified vermiculites were very fast and well fitted with pseudo-second-order kinetic model and Langmuir isotherm. PBS-VER exhibited the highest adsorption capacity (92.67 and 88.87 mg g−1 for BPA and TBBPA, respectively) than other two modified vermiculites in this order PBS-VER > BS-VER > SB-VER. The ionic strength (Na+, Ca2+) and coexisting compounds (Pb2+, humic acid) have different effects on the adsorption. PBS-VER had a good reusability and could remove ionic (methylene blue and orange G) and molecular (BPA) pollutants simultaneously and effectively due to the function of amphoteric hydrophilic groups and alkyl chains. The results might provide novel information for developing low-cost and effective adsorbents for removal of neutral and charged organic pollutants.

Based on detailed data from Chengdu Plain (CP) from 6 January to 16 January, two typical haze episodes were analyzed to clarify the haze formation mechanism in winter. Weather conditions, chemical compositions, secondary pollutant transformation, optical properties of aerosols, the potential source contribution function (PSCF) and source apportionment were studied. The planetary boundary layer (PBL) height decreased distinctly during the haze episodes and restrained air pollutant vertical dispersion. As the haze worsened, the value of PBL × PM2.5 increased notably. The [NO3−]/[SO42−] ratio was 0.61, 0.76 and 0.88 during a non-haze period, episode 1 and episode 2, respectively, indicating that the mobile source of the air pollution is increasingly predominant in Chengdu. Water vapor also played a vital role in the formation of haze by accelerating the chemical transformation of secondary pollutants, leading to the hygroscopic growth of aerosols. The PSCF and backward trajectories of the air masses indicated that the pollution mainly came from the south. The secondary inorganic aerosols, vehicle emissions, coal combustion, biomass burning, industry, and dust contributed 34.1%, 24.1%, 12.7%, 12.3%, 7.6%, and 7.2% to PM2.5 masses in episode 1 and 28.9%, 23.1%, 9.4%, 9.5%, 20.3% and 7.5% in episode 2.

Mineral phosphorus (P) fertilizers contain contaminants that are potentially hazardous to humans and the environment. Frequent mineral P fertilizer applications can cause heavy metals to accumulate and reach undesirable concentrations in agricultural soils. There is particular concern about Cadmium (Cd) and Uranium (U) accumulation because these metals are toxic and can endanger soil fertility, leach into groundwater, and be taken up by crops. We determined total Cd and U concentrations in more than 400 topsoil and subsoil samples obtained from 216 agricultural sites across Switzerland. We also investigated temporal changes in Cd and U concentrations since 1985 in soil at six selected Swiss national soil monitoring network sites. The mean U concentrations were 16% higher in arable topsoil than in grassland topsoil. The Cd concentrations in arable and grassland soils did not differ, which we attribute to soil management practices and Cd sources other than mineral P fertilizers masking Cd inputs from mineral P fertilizers. The mean Cd and U concentrations were 58% and 9% higher, respectively, in arable topsoil than in arable subsoil, indicating that significant Cd and U inputs to arable soils occurred in the past. Geochemical mass balances confirmed this, indicating an accumulation of 52% for Cd and 6% for U. Only minor temporal changes were found in the Cd concentrations in topsoil from the six soil-monitoring sites, but U concentrations in topsoil from three sites had significantly increased since 1985. Sewage sludge and atmospheric deposition were previously important sources of Cd to agricultural soils, but today mineral P fertilizers are the dominant sources of Cd and U. Future Cd and U inputs to agricultural soils may be reduced by using optimized management practices, establishing U threshold values for mineral P fertilizers and soils, effectively enforcing threshold values, and developing and using clean recycled P fertilizers.

Urban soil contamination with trace metals is a major obstacle to the development of urban agriculture as crops grown in urban gardens are prone to accumulate trace metals up to toxic levels for human consumption.Phytoextraction is considered as a potentially cost-effective alternative to conventional methods such as excavation. Field trials of phytoextraction with Noccaea caerulescens were conducted on urban soils contaminated with Cd, Cu, Pb, and Zn (respectively around 2, 150–200, 400–500, and 400–700 μg g−1 of dry soil). Metallicolous (Ganges population) and non-metallicolous (NMET) populations were compared for biomass production and trace metal uptake. Moreover, we tested the effect of compost and fertilizer addition. Maximal biomass of 5 t ha−1 was obtained with NMET populations on some plots. Compared to Ganges— the high Cd-accumulating ecotype from South of France often used in phytoextraction trials— NMET populations have an advantage for biomass production and for Zn accumulation, with an average Zn uptake of 2.5 times higher. The addition of compost seems detrimental due to metal immobilization in the soil with little or no effect on plant growth. In addition to differences between populations, variations of growth and metal accumulation were mostly explained by soil Cd and Zn concentrations and texture.Our field trials confirm the potential of using N. caerulescens for both Cd and Zn remediation of moderately contaminated soils—with uptake values of up to 200 g Cd ha−1 and 47 kg Zn ha−1—and show the interest of selecting the adequate population according to the targeted metal.

Organophosphate flame retardants (PFRs) can be rapidly metabolized in the body, and recent studies have shown that the di-alkyl phosphates (DAPs) are important metabolites. The accumulation and distribution of 8 PFRs and their 4 DAPs metabolites were first investigated in whole-body samples and various tissues of three freshwater fish species (topmouth gudgeon, crucian carp and loach) with different feeding habits from locations around Beijing, China. Concentrations of ΣPFRs in whole-body samples across all sampling locations ranged from 264.7 to 1973 ng g−1 lipid weight (lw), while all the paired DAP metabolites were detected in the total range from 35.3 to 510 ng g−1 lw. The calculated log bioconcentration factors (BCFs) of PFRs in whole fish were correlated with their log KOW (P < 0.05). The metabolite/parent ratios (MPRs) of ΣDAPs were calculated and ranged from 0.10 to 1.12 in whole-fish of all species. The MPRs of BBOEP/TBOEP were the highest. With respect to their distribution in different tissues, both the parent PFRs and metabolites were found at relatively higher levels in the liver than in other tissues (muscle, intestine, kidney and ovary), which was markedly different from those observed in avian species in previous studies. The accumulation of PFRs and DAPs in various tissues was not significantly correlated with the lipid content. The highest PFRs level in the liver may be related to the active hepatic accumulation processes. Meanwhile, the MPRs for all 4 pairs were the highest in the kidney relative to the other tissues. To the best of our knowledge, this is the first study of DAPs in the wild animals, and our study may improve the understanding of the accumulation and metabolism of PFRs in the body.

Samples of lichens, snow and particulate matter (PM10, 24 h) are used for the source identification of air pollution in the heavily industrialized region of Ostrava, Upper Silesia, Czech Republic. An integrated approach that uses different environmental samples for metal concentration and Pb isotope analyses was applied. The broad range of isotope ratios in the samples indicates a combination of different pollution sources, the strongest among them being the metallurgical industry, bituminous coal combustion and traffic. Snow samples are proven as the most relevant indicator for tracing metal(loid)s and recent local contamination in the atmosphere. Lichens can be successfully used as tracers of the long-term activity of local and remote sources of contamination. The combination of PM10 with snow can provide very useful information for evaluation of current pollution sources.