Ionizing radiation causes a variety of effects, including DNA damage associated to cancers. However, the effects in progeny from irradiated parents is not well documented. Using zebrafish as a model, we previously found that parental exposure to ionizing radiation is associated with effects in offspring, such as increased hatching rates, deformities, increased DNA damage and reactive oxygen species. Here, we assessed short (one month) and long term effects (one year) on gene expression in embryonic offspring (5.5 h post fertilization) from zebrafish exposed during gametogenesis to gamma radiation (8.7 or 53 mGy/h for 27 days, total dose 5.2 or 31 Gy) using mRNA sequencing. One month after exposure, a global change in gene expression was observed in offspring from the 53 mGy/h group, followed by embryonic death at late gastrula, whereas offspring from the 8.7 mGy/h group was unaffected. Interestingly, one year after exposure newly derived embryos from the 8.7 mGy/h group exhibited 2390 (67.7% downregulated) differentially expressed genes. Overlaps in differentially expressed genes and enriched biological pathways were evident between the 53 mGy/h group one month and 8.7 mGy/h one year after exposure, but were oppositely regulated. Pathways could be linked to effects in adults and offspring, such as DNA damage (via Atm signaling) and reproduction (via Gnrh signaling). Comparison with gene expression analysis in directly exposed embryos indicate transferrin a and cytochrome P450 2x6 as possible biomarkers for radiation response in zebrafish. Our results indicate latent effects following ionizing radiation exposure from the lower dose in parents that can be transmitted to offspring and warrants monitoring effects over subsequent generations.

Outdoor air pollution is considered as the most serious environmental problem for human health, associated with some million deaths worldwide per year. Cities have to cope with the challenges due to poor air quality impacting human health and citizen well-being. According to an analysis in the framework of this study, the annual mean concentrations of tropospheric ozone (O₃) have been increasing by on average 0.16 ppb year⁻¹ in cities across the globe over the time period 1995–2014. Green urban infrastructure can improve air quality by removing O₃. To efficiently reduce O₃ in cities, it is important to define suitable urban forest management, including proper species selection, with focus on the removal ability of O₃ and other air pollutants, biogenic emission rates, allergenic effects and maintenance requirements. This study reanalyzes the literature to i) quantify O₃ removal by urban vegetation categorized into trees/shrubs and green roofs; ii) rank 95 urban plant species based on the ability to maximize air quality and minimize disservices, and iii) provide novel insights on the management of urban green spaces to maximize urban air quality. Trees showed higher O₃ removal capacity (3.4 g m⁻² year⁻¹ on average) than green roofs (2.9 g m⁻² year⁻¹ as average removal rate), with lower installation and maintenance costs (around 10 times). To overcome present gaps and uncertainties, a novel Species-specific Air Quality Index (S-AQI) of suitability to air quality improvement is proposed for tree/shrub species. We recommend city planners to select species with an S-AQI>8, i.e. with high O₃ removal capacity, O₃-tolerant, resistant to pests and diseases, tolerant to drought and non-allergenic (e.g. Acer sp., Carpinus sp., Larix decidua, Prunus sp.). Green roofs can be used to supplement urban trees in improving air quality in cities. Urban vegetation, as a cost-effective and nature-based approach, aids in meeting clean air standards and should be taken into account by policy-makers.

In parallel to technological advances and ever-increasing use of nanoparticles in industry, agriculture and consumer products, the potential ecotoxicity of nanoparticles and their potential accumulation in ecosystems is of increasing concern. Because scientific reports raise a concern regarding nanoparticle toxicity to plants, understanding of their bioaccumulation has become critical and demands more research. Here, the synthesis of isotopically-labeled nanoparticles of silver, copper and zinc oxide is reported; it is demonstrated that while maintaining the basic properties of the same unlabeled (“regular”) nanoparticles, labeled nanoparticles enable more sensitive tracing of nanoparticles within plants that have background elemental levels. This technique is particularly useful for working with elements that are present in high abundance in natural environments. As a benchmark, labeled and unlabeled metal nanoparticles (Ag-NP, Cu-NP, ZnO-NP) were synthesized and compared, and then exposed in a series of growth experiments to Arabidopsis thaliana; the NPs were traced in different parts of the plant. All of the synthesized nanoparticles were characterized by TEM, EDS, DLS, ζ-potential and single particle ICP-MS, which provided essential information regarding size, composition, morphology and surface charge of nanoparticles, as well as their stability in suspensions. Tracing studies with A. thaliana showed uptake/retention of nanoparticles that is more significant in roots than in shoots. Single particle ICP-MS, and scanning electron micrographs and EDS of plant roots showed presence of Ag-NPs in particular, localized areas, whereas copper and zinc were found to be distributed over the root tissues, but not as nanoparticles. Thus, nanoparticles in any natural matrix can be replaced easily by their labeled counterparts to trace the accumulation or retention of NPs. Isotopically-labeled nanoparticles enable acquisition of specific results, even if there are some concentrations of the same elements that originate from other (natural or anthropogenic) sources.

Traffic emissions are a complex and variable cocktail of toxic chemicals. They are the major source of atmospheric pollution in the parts of cities where people live, commute and work. Reducing exposure requires information about the distribution and nature of emissions. Spatially and temporally detailed data are required, because both the rate of production and the composition of emissions vary significantly with time of day and with local changes in wind, traffic composition and flow. Increasing computer processing power means that models can accept highly detailed inputs of fleet, fuels and road networks. The state of the science models can simulate the behaviour and emissions of all the individual vehicles on a road network, with resolution of a second and tens of metres. The chemistry of the simulated emissions is also highly resolved, due to consideration of multiple engine processes, fuel evaporation and tyre wear. Good results can be achieved with both commercially available and open source models. The extent of a simulation is usually limited by processing capacity; the accuracy by the quality of traffic data. Recent studies have generated real time, detailed emissions data by using inputs from novel traffic sensing technologies and data from intelligent traffic systems (ITS). Increasingly, detailed pollution data is being combined with spatially resolved demographic or epidemiological data for targeted risk analyses.

The bioaccumulative, persistent and toxic properties of long-chain perfluoroalkyl acids (PFAAs) resulted in strict regulations on PFAAs, especially in developed countries. Consequently, the industry manufacturing of PFAAs shifts from long-chain to short-chain. In order to better understand the pollution situation of PFAAs in marine environment under this new circumstance, the occurrence of 17 linear PFAAs was investigated in 30 surface seawater samples from the North Pacific to Arctic Ocean (123°E to 24°W, 32 to 82°N) during the sixth Chinese Arctic Expedition in 2014. Total concentrations of PFAAs (∑PFAAs) were between 346.9 pg per liter (pg/L) to 3045.3 pg/L. The average concentrations of ∑PFAAs decreased in the order of East China Sea (2791.4 pg/L, n = 2), Sea of Japan (East Sea) (832.8 pg/L, n = 6), Arctic Ocean (516.9 pg/L, n = 7), Chukchi Sea (505.2 pg/L, n = 4), Bering Sea (501.2 pg/L, n = 8) and Sea of Okhotsk (417.7 pg/L, n = 3). C4 to C9 perfluoroalkyl carboxylic acids (PFCAs) were detected in more than 80% of the surface water samples. Perfluorobutanoic acid (PFBA) was the most prevalent compound and perfluorooctanoic acid (PFOA) was the second abundant homolog. The concentration of individual PFAAs in the surface seawater of East China Sea was much higher than other sampling seas. As the spatial distribution of PFAAs in the marine environment was mainly influenced by the river inflow from the basin countries, which proved the large input from China. Furthermore, the marginal seas of China were found with the greatest burden of PFOA comparing the pollution level in surface seawater worldwide. PFBA concentration in the surrounding seas of China was also high, but distributed more evenly with an obvious increase in recent years. This large-scale monitoring survey will help the improvement and development of PFAAs regulations and management, where production shift should be taken into consideration.

The sources of aerosol ammonium (NH4+) are of interest because of the potential of NH4+ to impact the Earth's radiative balance, as well as human health and biological diversity. Isotopic source apportionment of aerosol NH4+ is challenging in the urban atmosphere, which has excess ammonia (NH3) and where nitrogen isotopic fractionation commonly occurs. Based on year-round isotopic measurements in urban Beijing, we show the source dependence of the isotopic abundance of aerosol NH4+, with isotopically light (−33.8‰) and heavy (0 to +12.0‰) NH4+ associated with strong northerly winds and sustained southerly winds, respectively. On an annual basis, 37–52% of the initial NH3 concentrations in urban Beijing arises from fossil fuel emissions, which are episodically enhanced by air mass stagnation preceding the passage of cold fronts. These results provide strong evidence for the contribution of non-agricultural sources to NH3 in urban regions and suggest that priority should be given to controlling these emissions for haze regulation. This study presents a carefully executed application of existing stable nitrogen isotope measurement and mass-balance techniques to a very important problem: understanding source contributions to atmospheric NH3 in Beijing. This question is crucial to informing environmental policy on reducing particulate matter concentrations, which are some of the highest in the world. However, the isotopic source attribution results presented here still involve a number of uncertain assumptions and they are limited by the incomplete set of chemical and isotopic measurements of gas NH3 and aerosol NH4+. Further field work and lab experiments are required to adequately characterize endmember isotopic signatures and the subsequent isotopic fractionation process under different air pollution and meteorological conditions.

Cometabolism mechanisms of organic pollutants in environmental microbes have not been fully understood. In this study, a global analysis of Mycobacterium sp. strain A1-PYR transcriptomes on different PAH substrates (single or binary of pyrene (PYR) and phenanthrene (PHE)) was conducted. Comparative results demonstrated that expression levels of 23 PAH degradation enzymes were significantly higher in the binary substrate than in the PYR-only one. These enzymes constituted an integrated enzymatic system to actualize all transformation steps of PYR, and most of their encoded genes formed a novel gene cascade in the genome of strain A1-PYR. The roles of different genotypes of enzymes in PYR cometabolism were also discriminated even though all of their gene sequences were presented in the genome of this strain. NidAB and PdoA2B2 instead of NidA3B3 served the initial oxidization of PAHs, and PcaL replaced PcaCD to catalyze the formation of 3-oxoadipate. Novel genes associated with PYR cometabolism was also predicted by the relationships between their transcription profiles and PYR removal. The results showed that ABC-type transporters probably played important roles in the transport of PAHs and their metabolites through cell membrane, and [4Fe-4S] ferredoxin might be essential for dioxygenases (NidAB and PdoA2B2) to achieve oxidative activities. This study provided molecular insight in that microbial degrader subtly cometabolized recalcitrant PAHs with relatively more degradable ones.

Along the arid Arava, southern Israel, acacia trees (Acacia raddiana and Acacia tortilis) are considered keystone species. Yet they are threatened by the ongoing aquifer depletion for agriculture, the conversion of natural land to agricultural land, seed infestation by bruchid beetles, and the reduction in precipitation level in the region. In the acacia dominated Evrona reserve (southern Arava), adding to these threats are recurrent oil spills from an underground pipeline. We report here a study of the effects of contaminated soils, from a recent (December 2014) and a much older (1975) oil spills.The effects of local petroleum oil-contaminated soils on germination and early growing stages of the two acacia species were studied by comparisons with uncontaminated (control) soils from the same sites. For both acacia species, germination was significantly reduced in the 2014 oil-contaminated soils, whereas delayed in the 1975 oil-contaminated soil. There was no significant effect of oil volatile compounds on seed germination. At 105 days post transplanting (DPT), height, leaf number, stem diameter, and root growth were significantly smaller in the oil-contaminated soils. While photosynthetic performance (quantum yield of photosystem II) did not differ considerably between treatments, reductions of chlorophylls content and protein content were found in seedlings growing in the contaminated soils. Significant increases in superoxide dismutase (SOD) and ascorbate peroxidase (APX) activities were found in roots of seedlings growing in oil-contaminated soils. These results demonstrate that seed germination and seedling growth of both acacia species were strongly restricted by oil contamination in soils, from both recent (2014) and a 40-year old (1975) oil spills.Such long-term effects of oil spills on local acacia seedlings could shift the structure of local acacia communities. These results should be taken into account by local authorities aiming to clean up and restore such polluted areas.

Hourly concentrations of water-soluble inorganic ions (Na⁺, NH₄⁺, K⁺, Mg²⁺, Ca²⁺, Cl⁻, NO₃⁻ and SO₄²⁻) in PM₂.₅ and related reactive gases were measured with a Gas and Aerosol Collector combined with Ion Chromatography (GAC-IC) in urban Chengdu from April 17 to May 27, 2017, during which both haze and dust episodes occurred frequently. Nitrate was the most abundant ion in PM₂.₅ and substantially increased during haze pollution with the NO₃⁻/SO₄²⁻ mass ratio increasing from 0.78 during clean period to 1.1 during haze period. Aerosols in Chengdu were generally ammonium-rich, wherein ammonium nitrate was primarily formed through homogeneous gas-phase reactions and limited by the availability of HNO₃, indicating that preferentially reducing the emissions of NOx could make for mitigating spring haze pollution in Chengdu. Backward trajectory clustering coupled with measured species and a potential source contribution function (PSCF) for PM₂.₅, PM₁₀/PM₂.₅, sulfate, nitrate, ammonium, and Ca²⁺ indicated that regionally transported pollutants from the southern and southeastern Sichuan Basin strongly contributed to springtime PM₂.₅ pollution in Chengdu, but long-distance transport from northwestern China also contributed to dust pollution. Moreover, the treatment of urban fugitive dust in southern Sichuan is also important for reducing coarse particles in Chengdu. Therefore, the improvement of air quality in Chengdu, even in the Sichuan Basin, requires the regional joint emission reduction of particles and gaseous precursors across the entire Sichuan Basin, especially for cities located in southeastern Sichuan Basin.

A study was conducted in which the effluent at four small to medium sized sewage treatment plants (STP) in North Rhine-Westphalia, Germany was monitored for three pharmaceutical compounds (carbamazepine, diclofenac, metoprolol) over a period of four years. Grab sampling and auto sampling campaigns were accomplished with respect to various weather conditions in the catchment area. Flow volumes and hydraulic retention times (HRT) from various sampling dates which provide information on processes causing emission changes were additionally taken into account. Monitoring results showed that concentration scattering in the effluent is related to HRT in the sewage treatment plants. Dilution effects following rain events in the catchment area were analysed for the three investigated substances. Short-term emission changes explained by dilution only could be well determined by the mathematical relation between discharge and concentration, and for carbamazepine to be solely determined by the dilution effects at all HRTs. For metoprolol, a clear decrease in concentrations was observed at HRTs above 80 h, and a significant contribution of biodegradation was supported by independent biodegradation tests. For three out of the four STPs, a decrease in concentrations of diclofenac was observed at hydraulic retention times above 80 h, indicating removal, whereas the relationship between concentration and HRT of the other STP could be explained by dilution only. The study shows that emissions can vary with weather conditions, hampering the assessment of emissions and estimation of concentrations in surface waters from generic removal rates only. Furthermore, it illustrates the importance of HRT of rather stable substances in wastewater treatment.