Polychlorinated biphenyls (PCBs), one type of lipophilic pollutant, are ubiquitous in daily life. PCBs exposure has been implicated in the alterations of gut microbial community which is profoundly associated with diverse metabolic disorders, including obesity. High-fat diet (H) is a dietary pattern characterized by a high percentage of fat. According to the theory that similarities can be easily solvable in each other, PCBs and H exposures are inevitably and objectively coexistent in a real living environment, prompting great concerns about their individual and combined effects on hosts. However, the effects of PCBs-H interactions on gut microbiota and obesity are still incompletely understood. In the present study, the effects of PCBs and/or H on the gut microbiota alteration and obesity risk in mice were examined and the interactions between PCBs and H were investigated. Obtained results showed that PCBs and/or H exposure induced prominent variations in the gut microbiota composition and diversity. Exposure to PCBs also resulted in higher body fat percentage, greater size of abdominal subcutaneous adipocytes and increased expression of proinflammatory cytokines including TNF-α, iNOS and IL-6. Such PCBs-induced changes could be further enhanced upon the co-exposure of H, implying that obese individuals may be vulnerable to PCBs exposure. Taken together, the present study is helpful for a better understanding of the gut microbiota variation influenced by PCBs and/or H exposure, and furthermore, provides a novel insight into the mechanism of PCBs-H interactions on host adiposity.

Pollutant emissions from incomplete combustion of raw coal in low-efficiency residential heating stoves greatly contribute to winter haze in China. Semi-coke coals and improved heating stoves are expected to lower air pollutant emissions and are vigorously promoted by the Chinese government in many national and local plans. In this study, the thermal performance and air pollutant emissions from semi-coke combustion in improved heating stoves were measured in a pilot rural county and compared to the baseline of burning raw coal to quantify the mitigation potential of air pollutant emissions. A total of five stove-fuel combinations were tested, and 27 samples from 27 different volunteered households were obtained. The heating efficiency of improved stoves increased, but fuel consumption appeared higher with more useful energy output compared to traditional stoves. The emission factors of PM2.5, SO2, and CO2 of semi-coke burning in specified improved stoves were lower than the baseline of burning raw coal chunk, but no significant NOx and CO decreases were observed. The total amount of PM2.5 and SO2 emissions per household in one heating season was lower, but CO, CO2, and NOx increased when semi-coke coal and specified improved stoves were deployed. Most differences were not statistically significant due to the limited samples and large variation, indicating that further evaluation would be needed to make conclusions that could be considered for policy.

This article exploits a new approach for synthesis of polysaccharide-based grafted sodium styrene sulfonate (SSS) super absorbent hydrogels (SAHs) in aqueous solution by γ-radiation under ambient conditions. Important optimal conditions for preparation of hydrogels with the best swelling ratio, such as gamma irradiation dose and the ratio of feed composition have been discussed. Characterization techniques such as the SEM/EDS, FTIR and DSC were used in describing the newly prepared hydrogels. The FTIR gave characteristic peaks for -SO₃Na group at 1042 and 988 cm⁻¹, showing successful grafting of SSS onto the polysaccharide base material. The dependence of swelling behaviors in various pH solutions and salts solutions were investigated in detail. The prepared hybrid hydrogel showed most optimum swelling capacity at neutral pH whereas equilibrium swelling of SAHs was achieved within 5 h. The swelling of SAHs influenced obviously to metal ion removal percentage in solution.

Urban development has led to an increase in urban runoff, accompanied with a decrease in water quality during rain events. One of the major causes of the decrease in water quality is the presence of trace organic contaminants in urban runoff. However, little is known about the sources of organic contaminants in urban runoff, especially related to land-use and temporal trends in those associated land uses. The objective of this study was to assess the occurrence and concentration trends of organic contaminants for a high-density residential site and commercial strip site in Madison, WI. Flow-weighted samples of urban stormwater runoff, collected with an auto-sampler, were composited and analyzed, producing mean organic contaminants concentrations for each storm event. The contaminants, which include pesticides, flame retardants, polycyclic aromatic hydrocarbons, corrosion inhibitors, among others, were extracted and analyzed by gas chromatography coupled with mass spectrometry or liquid chromatography coupled with tandem mass spectrometry. There were 30 organic contaminants that had greater than 50% detections in at least one of the sites, and those organic contaminants did provide information on similarities and differences of organic contaminants in urban runoff derived from different land uses. The sum of the total measured pesticides showed no significant difference between sites; this was likely due to the considerable green space and associated pesticide use in both sites. However, there were higher total concentrations of organophosphate flame retardants and corrosion inhibitors in the residential site. The reason for this is unknown and will require follow-up studies; however, several hypotheses are presented. Conversely, there were higher total concentrations of polycyclic aromatic hydrocarbons in the commercial site; this is most likely due to higher vehicle traffic in the commercial site. These data show that land-use may be important in determining the composition and concentrations of trace organic contaminants in urban stormwater runoff.

Benzylalkyldimethylethyl ammonium compounds are pervasive in natural environments and toxic at high concentrations. The changes in functional genes and microbial diversity in eutrophic lake samples exposed to benzyldimethyldodecyl ammonium chloride (BAC) were assessed. BAC exerted negative effects on bacteria abundance, particularly at concentrations of 100 μg L−1 and higher. A significant increase in the number of the quaternary ammonium compound-resistant gene qacA/B was recorded within the 10 μg L−1 treatment after the first day of exposure. Not all antibiotic resistance genes increased in abundance as the concentrations of BAC increased; rather, gene abundances were dependent on the gene type, concentrations of BAC, and contact time. The nitrogen fixation-related gene nifH and ammonia monooxygenase gene amoA were inhibited by high concentrations of BAC after the first day, whereas an increase of the nitrite reductase gene nirK was stimulated by exposure. Microbial communities within higher treatment levels (1000 and 10 000 μg L−1) exhibited significantly different community composition compared to other treatment levels and the control. Selective enrichment of Rheinheimera, Pseudomonas, and Vogesella were found in the higher treatment levels, suggesting that these bacteria have some resistance or degradation capacity to BAC. Genes related with RNA processing and modification, transcription, lipid transport and metabolism, amino acid transport and metabolism, and cell motility of microbial community function were involved in the process exposed to the BAC stress.

The present experiment was conducted to explicate the genotoxic effects of profenofos, an organophosphate insecticide, on the erythrocytes of silver barb (Barbonymus gonionotus). Silver barb were exposed to a solution of 10% and 50% of lethal concentrations (LC₅₀) of profenofos as sub-lethal concentrations at different days (1, 7, 15, and 30 d), along with a control (0% profenofos). Subsequent recovery patterns were assessed allowing the fish exposed to profenofos free water for the same period that they were exposed to profenofos. Our results revealed that with the progression of time and concentration, fish exposed to profenofos showed significantly (p < .05) higher level of erythrocytic nuclear abnormalities (ENA) such as micronuclei, bi-nuclei, degenerated nuclei, notched nuclei, nuclear bridge and nuclear buds, as well as erythrocytic cellular abnormalities (ECA) such as echinocytic, elongated, fusion, spindle, tear-drop and twin shaped cells. After exposure, the silver barb recovered spontaneously, and the abnormal erythrocytic parameters were normalized with a concentration- and duration-dependent fashion. Therefore, these abnormalities and their recovery can be used to assess the toxic levels of pesticides on aquatic organisms. There is great potential to use this technique as in vivo to predict susceptibility of aquatic animals to environmental pollution.

It is desirable to establish an environmentally benign platform for disposing biomass from the phytoremediation process while recovering energy is of importance. To this end, the biochemical methane potential (BMP) tests were conducted using four different biomass samples (i.e., sunflower: Helianthus annuus) that were obtained from the different remediation sites. In particular, this study laid great emphasis on evaluating the inhibition for the anaerobic digestion (AD) process induced by endogenous heavy metal (Cd, Cu, Ni, Pb, and Zn) content in biomass. Despite the high levels of heavy metal contents (Cd: 58.4, Cu: 23.0, Ni: 2.01, Pb: 9.88, and Zn: 146 mg kg⁻¹) in the substrate for the AD process, the overall performance was comparable relative to the case of the references. Therefore, this study signified that the inhibition derived from heavy metals was nearly negligible, which suggested that biomass from the phytoremediation site could be used as a substrate for the AD process.

Following the widespread assumption that a majority of ubiquitous marine microplastic particles originate from land-based sources, recent studies identify rivers as important pathways for microplastic particles (MPP) to the oceans. Yet a detailed understanding of the underlying processes and dominant sources is difficult to obtain with the existing accurate but extremely time-consuming methods available for the identification of MPP.Thus in the presented study, a novel approach applying short-wave infrared imaging spectroscopy for the quick and semi-automated identification of MPP is applied in combination with a multitemporal survey concept. Volume-reduced surface water samples were taken from transects at ten points along a major watercourse running through the South of Berlin, Germany, on six dates. After laboratory treatment, the samples were filtered onto glass fiber filters, scanned with an imaging spectrometer and analyzed by image processing.The presented method allows to count MPP, classify the plastic types and determine particle sizes. At the present stage of development particles larger than 450 μm in diameter can be identified and a visual validation showed that the results are reliable after a subsequent visual final check of certain typical error types. Therefore, the method has the potential to accelerate microplastic identification by complementing FTIR and Raman microspectroscopy. Technical advancements (e.g. new lens) will allow lower detection limits and a higher grade of automatization in the near future.The resulting microplastic concentrations in the water samples are discussed in a spatio-temporal context with respect to the influence (i) of urban areas, (ii) of effluents of three major Berlin wastewater treatment plants discharging into the canal and (iii) of precipitation events. Microplastic concentrations were higher downstream of the urban area and after precipitation. An increase in microplastic concentrations was discernible for the wastewater treatment plant located furthest upstream though not for the other two.

In order to understand the impacts of regional emission changes and local tourism on sulfur and nitrogen wet deposition in Jiuzhaigou National Nature Reserve of southwestern China, wet deposition was monitored at a background site (Rize) and a tourist-affected site (PE: park entrance) in the reserve during 2015–2016. The observation data were compared between Rize and PE and between 2010–2011 and 2015–2016 monitoring campaigns. Also, the observation data were used in the Positive Matrix Factorization (PMF) model to identify the major sources of sulfur and nitrogen wet deposition. The results show that although local tourism emissions had considerable contributions to NH₄⁺, NO₂⁻, NO₃⁻, and SO₄²⁻ concentrations in wet deposition (p < 0.05), most of the annual Volume Weighted Mean (VWM) concentrations of these four ions were likely from emissions outside Jiuzhaigou. Annual wet deposition fluxes of the four ions were also affected more by precipitation and regional emissions than by local emissions. Although annual precipitation was higher at Rize (818 mm) during 2015–2016 than at another background site near Long Lake (LL: 752 mm) during 2010–2011, the annual concentrations and fluxes of SO₄²⁻ and NO₃⁻ wet deposition decreased by 77% and 74% for SO₄²⁻ and by 12% and 19% for NO₃⁻, respectively, most likely due to regional emission reductions. Similar large reductions in SO₄²⁻ and NO₃⁻ concentrations have been also found in some other sites in southwestern China. In contrast, the annual concentration and flux of NH₄⁺ wet deposition at Rize during 2015–2016 were 1.4 and 1.2 times of that measured at LL during 2010–2011, respectively. The results of source apportionment analysis and tour bus emission estimates suggest that elevated NH₄⁺ wet deposition was possibly related to NH₃ emissions from local tour buses, but additional studies on NH₃ emissions from tour buses in the reserve are needed to confirm this.

Data from an in situ monitoring network and five ozone sondes are analysed during August of 2012, and a high tropospheric ozone episode is observed around the 8th of AUG. The Community Multi-scale Air Quality (CMAQ) model and its process analysis tool were used to study factors and mechanisms for high ozone mixing ratio at different levels of ozone vertical profiles. A sensitive scenario without chemical initial and boundary conditions (ICBCs) from MOZART4-GEOS5 was applied to study the impact of stratosphere-troposphere exchange (STE) on vertical ozone. The simulation results indicated that the first high ozone peak near the tropopause was dominated by STE. Results from process analysis showed that: in the urban area, the second peak at approximately 2 km above ground height was mainly caused by local photochemical production. The third peak (near surface) was mainly caused by the upwind transportation from the suburban/rural areas; in the suburban/rural areas, local photochemical production of ozone dominated the high ozone mixing ratio from the surface to approximately 3 km height. Furthermore, the capability of indicators to distinguish O3-precursor sensitivity along the vertical O3 profiles was investigated. Two sensitive scenarios, which had cut 30% anthropogenic NOX or VOC emissions, showed that O3-precursor indicators, specifically the ratios of O3/NOy, H2O2/HNO3 or H2O2/NOZ, could partly distinguish the O3-precursor sensitivity between VOCs-sensitive and NOx-sensitive along the vertical profiles. In urban area, the O3-precursor relationship transferred from VOCs-sensitive within the boundary layer to NOx-sensitive at approximately 1–3 km above ground height, further confirming the dominant roles of transportation and photochemical production in high O3 peaks at the near-ground layer and 2 km above ground height, respectively.