Heze city, a medium-size city in Shandong province, Eastern China. Ambient PM2.5 samples were collected in urban area of Heze from August 2015 to April 2016, and chemical species and sources of PM2.5 were investigated in this paper. The results indicated that the average concentration of PM2.5 was 100.9 μg/m3 during the sampling period, and the water-soluble ions, carbonaceous species included elemental carbon (EC) and organic carbon (OC), as well as elements contributed 32.7–51.7%, 16.3% and 12.5%, respectively, to PM2.5. Pearson's correlation analysis showed that the existing form of NH4+ was more complex and diverse in spring/summer, and ammonium nitrate, ammonium sulfate and ammonium hydrogen sulfate might be major form of NH4+ in autumn/winter. Correlation analysis between PM2.5 and SO42−/NO3−, PM2.5 and OC/EC during different seasons suggested that mobile sources might make an important impact on the increase of PM2.5 concentrations in spring/summer, and stationary sources might play a critical role on the increase of PM2.5 concentrations in autumn/winter. Seven factors were selected in Positive Matrix Factorization (PMF) models analysis based on the Error Estimation (EE) diagnostics during different seasons. Secondary source had the highest contribution to PM2.5 in Heze for the whole year, and followed by coal combustion, vehicle exhaust, soil dust, construction dust, biomass burning and metal manufacturing, and their annual contributions to PM2.5 were 26.5%, 17.2%, 16.5%, 11.5%, 7.7%, 7.0% and 3.8%, respectively. The air masses that were originated from Mongolia reflected the features of large-scale and long-distance air transport; while the air masses that began in Jiangsu, Shandong and Henan showed the features of small-scale and short-distance. Shandong, Henan and Jiangsu were identified as the major potential sources-areas of PM2.5 by using potential source contribution function (PSCF) and concentration-weighted trajectory (CWT) models.

The impacts of iron oxide nanoparticles (γ-Fe2O3 NPs) and ferric ions (Fe³⁺) on plant growth and molecular responses associated with the transformation and transport of Fe²⁺ were poorly understood. This study comprehensively compared and evaluated the physiological and molecular changes of Citrus maxima plants as affected by different levels of γ-Fe2O3 NPs and Fe³⁺. We found that γ-Fe2O3 NPs could enter plant roots but no translocation from roots to shoots was observed. 20 mg/L γ-Fe2O3 NPs had no impact on plant growth. 50 mg/L γ-Fe2O3 NPs significantly enhanced chlorophyll content by 23.2% and root activity by 23.8% as compared with control. However, 100 mg/L γ-Fe2O3 NPs notably increased MDA formation, decreased chlorophyll content and root activity. Although Fe³⁺ ions could be used by plants and promoted the synthesis of chlorophyll, they appeared to be more toxic than γ-Fe2O3 NPs, especially for 100 mg/L Fe³⁺. The impacts caused by γ-Fe2O3 NPs and Fe³⁺ were concentration-dependent. Physiological results showed that γ-Fe2O3 NPs at proper concentrations had the potential to be an effective iron nanofertilizer for plant growth. RT-PCR analysis showed that γ-Fe2O3 NPs had no impact on AHA gene expression. 50 mg/L γ-Fe2O3 NPs and Fe³⁺ significantly increased expression levels of FRO2 gene and correspondingly had a higher ferric reductase activity compared to both control and Fe(II)-EDTA exposure, thus promoting the iron transformation and enhancing the tolerance of plants to iron deficiency. Relative levels of Nramp3 gene expression exposed to γ-Fe2O3 NPs and Fe³⁺ were significantly lower than control, indicating that all γ-Fe2O3 NPs and Fe³⁺ treatments could supply iron to C. maxima seedlings. Overall, plants can modify the speciation and transport of γ-Fe2O3 NPs or Fe³⁺ for self-protection and development by activating many physiological and molecular processes.

Crotonaldehyde is an ubiquitous hazardous pollutant in the environment which can be produced naturally, artificially and endogenously. Acute exposure of crotonaldehyde was reported to induce severe lung injury in humans and experimental animals. However, the exact toxicity mechanisms of crotonaldehyde in organisms have not been fully explored. In the present study, we explored the role autophagy played in the cytotoxicity induced by crotonaldehyde in human bronchial epithelial cells (BEAS-2B), and the pathways that mediated autophagy, including the phosphatidylinositol 3-kinase (PI3K) pathway, the AMP-activated protein kinase (AMPK) pathway and the mitogen-activated protein kinase (MAPK) pathways, were examined and validated. We found that crotonaldehyde induced cytotoxicity and autophagy simultaneously in BEAS-2B cells, and blockage of autophagic flux significantly elevated the viability of BEAS-2B exposed to high concentrations of crotonaldehyde. Crotonaldehyde down-regulated the activity of PI3K pathway, and elevated the activities of AMPK and MAPK pathways. Pretreatment of specific agonist or antagonist of these pathways could inhibit autophagy and partly improve the viability. These results suggested that acute exposure of crotonaldehyde induced cell death mediated by autophagy, which might be helpful to elucidate the toxicity mechanisms of crotonaldehyde and contribute to environmental and human health risk assessment.

Filamentous plastic litter collected from two beaches in south west England has been characterized by FTIR and XRF. The majority of samples were constructed of polyethylene and consisted of twisted or braided strands of a variety of colours that appeared to be derived from commercial fishing nets. A number of different elements were detected among the samples but, from an environmental perspective, the regular occurrence of Cr and Pb and the occasional or isolated occurrence of Br, Cd and Se were of greatest concern. The highest total concentrations of Br (2420 μg g⁻¹), Cd (1460 μg g⁻¹), Cr (909 μg g⁻¹), Pb (3770 μg g⁻¹) and Se (240 μg g⁻¹) were always encountered among orange samples and are attributed to the presence of lead chromates and cadmium sulphoselenide as colourants and to brominated compounds as flame retardants. Element bioaccessibility was evaluated by ICP-MS following an acidic extraction test that mimics the digestive tract of seabirds, with maximum values after a seven-day incubation period and relative to respective total concentrations of 0.2–0.4% for Cd, Cr and Pb and about 7% for Br. In addition to the well-documented impacts on wildlife through entrapment, filamentous plastic waste may act as a significant source of hazardous chemicals into the marine foodchain through ingestion.

Extracellular polymeric substances (EPS) isolated from bacteria, are abound of functional groups which can react with metals and consequently influence the immobilization of metals. In this study, we combined with Zn K-edge Extended X-ray Absorption Fine Structure (EXAFS), Fourier Transform Infrared (FTIR) spectroscopy, and High-Resolution Transmission Electron Microscopy (HRTEM) techniques to study the effects of EPS isolated from Bacillus subtilis and Pseudomonas putida on Zn sorption on γ-alumina. The results revealed that Zn sorption on aluminum oxide was pH-dependent and significantly influenced by bacterial EPS. At pH 7.5, Zn sorbed on γ-alumina was in the form of Zn-Al layered doubled hydroxide (LDH) precipitates, whereas at pH 5.5, Zn sorbed on γ-alumina was as a Zn-Al bidentate mononuclear surface complex. The amount of sorbed Zn at pH 7.5 was 1.3–3.7 times higher than that at pH 5.5. However, in the presence of 2 g L−1 EPS, regardless of pH conditions and EPS source, Zn + EPS + γ-alumina ternary complex was formed on the surface of γ-alumina, which resulted in decreased Zn sorption (reduced by 8.4–67.8%) at pH 7.5 and enhanced Zn sorption (increased by 10.0–124.7%) at pH 5.5. The FTIR and EXAFS spectra demonstrated that both the carboxyl and phosphoryl moieties of EPS were crucial in this process. These findings highlight EPS effects on Zn interacts with γ-alumina.

Bromide is a conservative tracer that is often applied with non-conservative solutes such as pesticides to estimate their retardation in the soil. It has been applied in concentrations of up to 250 g Br L−1, levels at which the growth of single-celled organisms can be inhibited. Bromide applications may therefore affect the biodegradation of non-conservative solutes in soil.The present study investigated the effect of potassium bromide (KBr) on the mineralisation of three pesticides – glyphosate, MCPA and metribuzin – in four agricultural A-horizon soils. KBr was added to soil microcosms at concentrations of 0, 0.5, 2.5 and 5 g Br− L−1 in the soil solution. The study concluded that KBr had a negative effect on pesticide mineralisation. The inhibitory effect varied depending on the KBr concentration, the type of pesticide and the type of soil. Furthermore, 16 S amplicon sequencing revealed that the KBr treatment generally reduced the abundance of bacteroidetes and proteobacteria on both an RNA and DNA level.Therefore, in order to reduce the effect of KBr on the soil bacterial community and consequently also on xenobiotic degradation, it is recommended that KBr be applied in a concentration that does not exceed 0.5 g Br− L−1 in the soil water.

Accurate measurement of ammonia (NH3) emissions from livestock pens is challenging. Two micrometeorological techniques, the integrated horizontal flux (IHF) and the backward Lagrangian stochastic (bLS) dispersion technique were used to measure NH3 emissions from an isolated cattle pen (20 × 20 m) in Victoria, Australia. The bLS technique is simple and insensitive to the presence of animals, but typically gives discontinuous measurements due to the need for target wind directions and wind conditions above accepted thresholds. In contrast, the IHF technique as implemented here gives near-continuous measurements with no restriction on wind directions. However, IHF needs more complex field measurements, and there are ambiguities when applied to an animal pen due to the presence of animals. Over the 29 days of our experiment, we collected 124 coincidental bLS and IHF emission measurements from the pen (30−min each). We found no statistical difference in the bLS and IHF calculations when the IHF turbulent flux correction factor (TFcor) was set to 15%. Our results confirm that the IHF and bLS techniques, using independent sensors and having very different equipment layouts, gives nearly equivalent results. This suggests the choice of the two methods in future experiments can focus on their different strengths and weaknesses.

Polybrominated diphenyl ethers (PBDEs) are still present in sewage sludge and sludge-amended soil, even though commercial PBDEs were prohibited or voluntarily phased out several years ago. In this study, levels and compositional profiles of seven major PBDE congeners in sludge are assessed in relation to their usage patterns in commercial products, and years of being banned and phased out in North America, Europe, and Asia. Annual accumulations and future long-term changes of PBDE in sludge-amended soil are estimated. BDE-209 has the highest concentration, followed by BDE-99 and BDE-47. The highest concentrations, up to 23,500 ng g−1, of PBDEs in sludge were found in North America until 2004–2007, whereas since then sludge PBDE concentrations, up to 6600 ng g−1 have been higher in Asia than on the other two continents. The amount of sludge applied and the soil organic matter content play important roles in determining PBDE concentrations in sludge-amended soil. The estimated concentrations of BDE-47, -99, and -209 in soils receiving sludge applications during the past 15 years are 40–300 times higher than in soils after the initial sludge application. The accumulated concentrations of BDE-47 and BDE-99 are expected to decrease by 99% between 2016 and 2100, whereas the decrease in the BDE-209 concentration is predicted to be approximately 87%.

Hexachlorobenzene (HCB) and pentachlorobenzene (PeCBz) have been listed as unintentional POPs in the annex of the Stockholm Convention and thus, attracted attention by government and researchers. Since the intentional production and use has ceased in most countries, the unintentional releases to the environment have increased. This study gathered 206 and 78 emission factors (EFs) of unintentional HCB and PeCBz from scientific publications and governmental reports, respectively. Most of the EFs referred to the release vector “air” (EFAir) and to a less extent to “product” (EFProduct). EFs were proposed for different source categories/classes used in the Toolkit according to the technologies that released the HCB or PeCBz. Overall, lowest and highest EFAir for HCB were found in the metallurgical industry range from 1 μg/t in well controlled plants (coke, iron and steel) up to 40,000 μg/t (secondary zinc). EFs for PeCBz were in similar order of magnitude. Due to lack of data, EFs to water, land or residue cannot be proposed. Using linear regression and statistical analysis such as Pearson correlation, we found strongest correlation of EFAir between HCB and PeCBz (R2 = 0.79, P < 0.01) and weaker, but still significant, correlations for EFAir between PCDD/PCDFTEQ and HCB (R2 = 0.56; P < 0.01) or PeCBz (R2 = 0.31 P < 0.01) for various thermal processes.

The recent discovery of pyrethroid-resistant Hyalella azteca populations in California, USA suggests there has been significant exposure of aquatic organisms to these terrestrially-applied insecticides. Since resistant organisms are able to survive in relatively contaminated habitats they may experience greater pyrethroid bioaccumulation, subsequently increasing the risk of those compounds transferring to predators. These issues were evaluated in the current study following toxicity tests in water with permethrin which showed the 96-h LC50 of resistant H. azteca (1670 ng L⁻¹) was 53 times higher than that of non-resistant H. azteca (31.2 ng L⁻¹). Bioaccumulation was compared between resistant and non-resistant H. azteca by exposing both populations to permethrin in water and then measuring the tissue concentrations attained. Our results indicate that resistant and non-resistant H. azteca have similar potential to bioaccumulate pyrethroids at the same exposure concentration. However, significantly greater bioaccumulation occurs in resistant H. azteca at exposure concentrations non-resistant organisms cannot survive. To assess the risk of pyrethroid trophic transfer, permethrin-dosed resistant H. azteca were fed to fathead minnows (Pimephales promelas) for four days, after which bioaccumulation of permethrin and its biotransformation products in fish tissues were measured. There were detectable concentrations of permethrin in fish tissues after they consumed dosed resistant H. azteca. These results show that bioaccumulation potential is greater in organisms with pyrethroid resistance and this increases the risk of trophic transfer when consumed by a predator. The implications of this study extend to individual fitness, populations and food webs.