We evaluated the short-term effect of mixtures of ambient air pollutants on respiratory and circulatory morbidity in four Colombian cities.Daily Emergency Department (ED) visit records for respiratory and circulatory selected diagnosis and daily concentrations for six criteria air pollutant were obtained in four of the five major cities in Colombia: Bucaramanga, Bogota, Cali, and Medellin during 2011–2014. Using conditional Poisson time series analysis with fixed effects, we assessed the effect of air pollutants on health outcomes using single-pollutant, two-pollutant and specific mixtures-of-pollutant models controlling for meteorology and time trends. The percentages of change in the rate of ED visits and their 95% confidence interval were estimated for the joint effect of pollutants.In single-pollutant models increases in gases concentrations were associated with increases in ED visits for respiratory and circulatory diseases. The two-pollutant models for respiratory diseases showed that the effect of NO₂ alone (% change 2.86 95% CI 1.87–3.85) is higher than the joint effect of any of its combinations except for its combination with SO₂ (% change 3.05 95%CI 1.04–5.05). The two-pollutant models for circulatory diseases showed synergistic effects between NO₂ and PM₂.₅ (% change 2.13 95%CI 0.001–4.26). Specific mixtures models showed that the mixture of “traffic-related pollutants” has the higher joint effect on circulatory morbidity and respiratory morbidity.The results show the dominant effect of NO₂ in air pollution mixtures on respiratory and circulatory morbidity, and the synergistic effect of NO₂ and SO₂ in air pollution mixtures on respiratory morbidity.

As the second largest economy in the world, China experiences severe particulate matter (PM) pollution in many of its cities. Meteorological factors are critical in determining both areal and temporal variations in PM pollution levels; understanding these factors and their interactions is critical for accurate forecasting, comprehensive analysis, and effective reduction of this pollution. This study analyzed areal and temporal variations in concentrations of PM₂.₅, PM₁₀, and PMcₒₐᵣₛₑ (PM₁₀ - PM₂.₅) and PM₂.₅ to PM₁₀ ratios (PM₂.₅/PM₁₀) and their relationships with meteorological conditions in 366 Chinese cities from January 1, 2015 to December 31, 2017. On the national scale, PM₂.₅ and PM₁₀ decreased from 48 to 42 μg m⁻³ and from 88 to 84 μg m⁻³, respectively, and the annual mean concentrations were 45 μg m⁻³ (PM₂.₅) and 84 μg m⁻³ (PM₁₀) during the time period (2015–2017). In most regions, largest PM concentrations occurred in winter. However, in northern China, in spring PMcₒₐᵣₛₑ concentrations were highest due to dust. The PM₂.₅/PM₁₀ ratio was higher in southern than in northern China. There were large regional disparities in PM diurnal variations. Generally, PM concentrations were negatively correlated with precipitation, relative humidity, air temperature, and wind speed, but were positively correlated with surface pressure. The sunshine duration showed negative and positive impacts on PM in northern and southern cities, respectively. Meteorological factors impacted particulates of different size differently in different regions and over different periods of time.

Pollutants, which are usually transported from urban cities to remote glacier basins, and aerosol impurities affect the earth's temperature and climate by altering the radiative properties of the atmosphere. This work focused on the physicochemical properties of atmospheric pollutants across the urban and remote background sites in northwest China. Information on individual particles was obtained using transmission electron microscopy (TEM) and energy dispersive X-ray spectrometry (EDX). Particle size and age-dependent mixing structures of individual particles in clean and polluted air were investigated. Aerosols were classified into eight components: mineral dust, black carbon (soot)/fly ash, sulfates, nitrates, NaCl salt, ammonium, organic matter, and metals. Marked spatial and seasonal changes in individual particle components were observed in the study area. Aerosol particles were generally found to be in the mixing state. For example, salt-coated particles in summer accounted for 31.2–44.8% of the total particles in urban sites and 37.5–74.5% of the total particles in background sites, while in winter, almost all urban sites comprised >50%, which implies a significant effect on the radiative forcing in the study area. We found that in PM₂.₅ section, the internally mixed black carbon/organic matter particles clearly increased with diameter. Moreover, urban cities were characterized by atmospheric particles sourced from anthropogenic activities, whereas background locations exhibited much lower aerosol concentrations and increased particle density, originating from natural crustal sources (e.g., mineral dust and NaCl salt), which, together with air mass trajectory analysis, indicates a potential spatial transport process and routes of atmospheric transport from urban cities to background locations. Thus, this work is of importance in evaluating atmospheric conditions in northwest China and northeast Tibetan Plateau regions, to discover the transport processes and facilitate improvements in climatic patterns concerning atmospheric impurities.

While migratory seabirds dominate ecotoxicological studies within the Arctic, there is limited knowledge about exposure and potential effects from circulating legacy and emerging contaminants in species who reside in the high-Arctic all year round. Here, we focus on the case of the Mandt's Black guillemot (Cepphus grylle mandtii) breeding at Kongsfjorden, Svalbard (79.00°N, 11.66°E) and investigate exposure to legacy and emerging contaminants in relation to individual physiological status, i.e. body condition, oxidative stress and relative telomere length. Despite its benthic-inshore foraging strategy, the Black guillemot displayed overall similar contaminant concentrations in blood during incubation (∑PCB11 (15.7 ng/g w.w.) > ∑PFAS5 (9.9 ng/g w.w.) > ∑Pesticides9 (6.7 ng/g w.w.) > ∑PBDE4 (2.7 ng/g w.w.), and Hg (0.3 μg/g d.w.) compared to an Arctic migratory seabird in which several contaminant-related stress responses have been observed. Black guillemots in poorer condition tended to display higher levels of contaminants, higher levels of reactive oxygen metabolites, lower plasmatic antioxidant capacity, and shorter telomere lengths; however the low sample size restrict any strong conclusions. Nevertheless, our data suggests that nonlinear relationships with a threshold may exist between accumulated contaminant concentrations and physiological status of the birds. These findings were used to build a hypothesis to be applied in future modelling for describing how chronic exposure to contaminants may be linked to telomere dynamics.

The high acidity of mercury ions (Hg²⁺) contained wastewater can complicate its safe disposal. MgAl-LDHs supported [SnS₄]⁴⁻ clusters were synthesized for Hg²⁺ removal from acid wastewater. The active sites of [SnS₄]⁴⁻ clusters were inserted into the interlayers of MgAl-LDHs using an ion-exchange method. The experimental results indicated that [SnS₄]⁴⁻/MgAl-LDHs composite can obtain higher than 99% Hg²⁺ removal efficiency under low pH values. The maximum mercury adsorption capacity is 360.6 mg g⁻¹. It indicated that [SnS₄]⁴⁻ clusters were the primary active sites for mercury uptake, existing as stable Hg₂(SnS₄) on the surface of the composite. Under low pH values, such a composite seems like a “net” for HgSO₄ molecules, exhibiting great potential for mercury removal from acid solutions. Moreover, the co-exist metal ions such as Zn²⁺, Na⁺, Cd²⁺, Cr³⁺, Pb²⁺, Co²⁺, and Ni²⁺ have no significant influences on Hg²⁺ removal. The adsorption isotherms and kinetics were also studied, indicating that the adsorption mechanism follows a monolayer chemical adsorption model. The [SnS₄]⁴⁻/MgAl-LDHs composite exhibits a great potential for Hg²⁺ removal from acid wastewater.

A comprehensive analysis of 15 target chemical compounds (pharmaceuticals and personal care product, perfluoroalkyl compounds and industrial chemicals) were carried out to determine their concentrations in selected commercially exploited, wild caught small and medium sized pelagic fish species and their organs (Thyrsites atun (snoek), Sarda orientalis (bonito), Pachymetopon blochii (panga) and Pterogymnus laniarius (hottentot)) obtained from Kalk Bay harbour, Cape Town. Solid phase extraction (SPE) method based on Oasis HLB cartridges were used to concentrate and clean-up the samples. Liquid chromatography–mass spectrometry analysis of these chemical compounds revealed the simultaneous presence of at least 12 compounds in different parts of the selected fish species in nanogram-per-gram dry weight (ng/g dw) concentrations. The results revealed that perfluorodecanoic acid, perfluorononanoic acid and perfluoroheptanoic acid were the most predominant among the perfluorinated compounds and ranged between: (20.13–179.2 ng/g), (21.22–114.0 ng/g) and (40.06–138.3 ng/g). Also, diclofenac had the highest concentration in these edible fish species out of all the pharmaceuticals detected (range: 551.8–1812 ng/g). The risk assessment values were above 0.5 and 1.0 for acute and chronic risk respectively which shows that these chemicals have a high health risk to the pelagic fish, aquatic organisms and to humans who consume them. Therefore, there is an urgent need for a precautionary approach and the adequate regulation of the use and disposal of synthetic chemicals that persist in aquatic/marine environment in this province and other parts of South Africa, to prevent impacts on the sustainability of our marine environment, livelihood and lives.

High performance activated carbon (HPAC) supported nanoscale zerovalent iron (nZVI) was prepared and used for recovery of silver. This composite material was characterized by Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and X-ray diffraction (XRD). The removal amount of Ag+ increased with pH values and temperature. The removal process achieved equilibrium within 40 min and the maximum removal capacity was 986.5 mg/g at 298 K. The composite material showed fast adsorption rate and high adsorption capacity because the presence of high surface area activated carbon could effectively inhibit aggregation of nanoscale zerovalent iron, thus enhancing its reactivity. The Ag+ removal followed pseudo-second-order kinetic model and Langmuir isotherm model. XPS and XRD characterizations were performed to elucidate removal mechanism. It could be concluded that both coordination adsorption and reductive precipitation contributed to removal of Ag+ on the nZVI/HPAC.

Anthropogenic Pb emitted from East Asia, particularly China, is often long-range transported to the east by the prevailing westerlies. To characterize the geographical properties of varying atmospheric Pb concentrations by transboundary and domestic source(s)-related Pb in Korea, closely adjacent to China, the Al and Pb concentrations and the stable Pb isotopic composition were determined in the total suspended particles (TSP) collected at urban (IC), rural (TA), and remote background (JJ) sites in western Korea from August 2015 to October 2016. The annual average Pb concentrations were significantly higher in urban and rural areas (IC, 16.2 ng m⁻³ and TA, 11.1 ng m⁻³) than in remote area (JJ, 6.41 ng m⁻³), showing pronounced seasonal variations with relatively higher concentrations in winter and spring and lower concentrations in summer and autumn. Significantly high enrichment factors (EF) for Pb indicate that anthropogenic contributions are important for this toxic element in TSP. Coupling the Pb isotopic signatures with the air mass back trajectories identified the major potential source regions for individual samples. The results show that during winter, China was the dominant contributor, accounting for 92%, 82%, and 100% of the sampling periods at IC, TA, and JJ, respectively. The Chinese contribution decreased in summer and autumn, whereas the Korean contribution increased, according to the East Asian monsoon system. The Pb concentrations increased by 2.2 (IC), 1.2 (TA) and 1.4 (JJ) times when the Chinese contribution was dominant, compared to the Korea-dominant periods. The Pb isotopic systematics for the samples characterized by the dominant Korean contribution differed substantially between the three sites, implying that the relative importance of various domestic sources varied with geographical areas in western Korea.

As one of the highest energy consuming and polluting industries, the power generation industry is an important source of particulate matter emissions. Recently, implementation of ultra-low emission technology has changed the emission characteristic of fine particulate matter (PM2.5). In this study, PM2.5 emitted from four typical power plants in China was sampled using a dilution channel sampling system, and analyzed for elements, water-soluble ions and carbonaceous fractions. The results showed that PM2.5 concentrations emitted from the four power plants were 0.78 ± 0.16, 0.63 ± 0.09, 0.29 ± 0.07 and 0.28 ± 0.01 mg m−3, respectively. Emission factors were 0.004–0.005 g/kg coal, nearly 1–2 orders of magnitude lower than those reported in previous studies. The highest proportions of PM2.5 consisted of organic carbon (OC), SO42−, elemental carbon (EC), NH4+, Al and Cl−. Coefficients of divergence (CDs) were in the ranges 0.22–0.41 (for an individual plant), 0.43–0.69 (among different plants), and 0.60–0.99 (in previous studies). The results indicated that the source profiles of each tested power plant were relatively similar, but differed from those in previous studies. Enrichment factors showed elevated Se and Hg, in accordance with the source markers Se and As. Comparing source profiles with previous studies, the proportion of OC, EC and NH4+ were higher, while the proportion of Al in PM2.5 were relatively lower. The OC/EC ratio became concentrated at ∼5. Results from this study can be used for source apportionment and emission inventory calculations after implementation of ultra-low emission technologies.

Ambient particulate pollution, especially PM₂.₅, has adverse impacts on health and welfare. To manage and control PM₂.₅ pollution, it is of great importance to determine the factors that affect PM₂.₅ levels. Previous studies commonly focused on a single or several cities. This study aims to analyze the impacts of meteorological and socio-economic factors on daily concentrations of PM₂.₅ in 109 Chinese cities from January 1, 2015 to December 31, 2015.To evaluate potential risk factors associated with the spatial and temporal variations in PM₂.₅ levels, we developed a Bayesian spatio-temporal model in which the potential temporal autocorrelation and spatial autocorrelation of PM₂.₅ levels were taken into account to ensure the independence of the error term of the model and hence the robustness of the estimated parameters.Daily concentrations of PM₂.₅ peaked in winter and troughed in summer. The annual average concentration reached its highest value (79 μg/m³) in the Beijing-Tianjin-Hebei area. The city-level PM₂.₅ was positively associated with the proportion of the secondary industry, the total consumption of liquefied petroleum gas and the total emissions of industrial sulfur dioxide (SO₂), but negatively associated with the proportion of the primary industry. A reverse U-shaped relationship between population density and PM₂.₅ was found. The city-level and daily-level of weather conditions within a city were both associated with PM₂.₅.PM₂.₅ levels had significant spatio-temporal variations which were associated with socioeconomic and meteorological factors. Particularly, economic structure was a determinant factor of PM₂.₅ pollution rather than per capita GDP. This finding will be helpful for the intervention planning of particulate pollution control when considering the environmental and social-economic factors as part of the strategies.