Studies of the chemical composition of atmospheric aerosols, rain water and snow in various regions of the globe quite often show the presence of pyridine and a number of its low mass derivatives. Nevertheless, the sources of those compounds in the environment have not yet been established and definitely require elucidation, supported by reliable experimental results. In the present work the chemical composition of peat combustion products as one of the important sources of atmospheric aerosol emission is studied by two-dimensional gas chromatography – high-resolution mass spectrometry with a focus on the detection of pyridine derivatives. Twenty-five compounds of this class were reliably identified and quantified in laboratory experiments on peat burning. Among them 3-hydroxypyridine predominates, while the rest analytes are mostly represented by alkyl derivatives: pyridine, 2-methylpyridine, 3-methylpyridine, 2,5-dimethylpyridine, 2,6-dimethylpyridine, 2-ethylpyridine, lutidines (in order of decreasing concentration). The distribution of these combustion products coincides with that obtained earlier in environmental studies carried out in Arctic, Central Russia and France. The experiments on peat thermal decomposition by pyrolysis GC-MS demonstrated that the maximum concentrations as well as the number of detected analytes were found under conditions of oxygen lack and a temperature of about 500 °C, i.e. characteristic conditions of peat wildfires. The observed levels of pyridines’ emission recalculated on the peat dry weight exceeded 200 mg kg⁻¹. Considering hundreds of millions tons of peat burning in megafires over 20,000 tons of pyridines penetrate the Earth atmosphere annually. The obtained results allow concluding that peat burning may be the major and still underestimated source of pyridine and lower alkylpyridines in the Earth atmosphere.

The 22ⁿᵈ Asia-Pacific Economic Cooperation (APEC) Conference was held near Yanqi Lake, Huairou, in Beijing, China during November 10-11, 2014. To guarantee haze-free days during the APEC Conference, the Beijing government and the governments of the surrounding provinces implemented a series of controls. Three months of Aethalometer 880 nm black carbon (BC) measurements were examined to understand the hourly fluctuations in BC concentrations that resulted from emission controls and meteorology changes. Measurements were collected at the University of Chinese Academy of Sciences near the APEC Conference site and in Central Beijing at the Institute of Remote Sensing and Digital Earth of the Chinese Academy of Sciences. Synoptic conditions are successfully represented through analysis of backward trajectories in six cluster groups. The clusters are identified based on air mass transport from various areas such as Inner Mongolia, Russia, three northeastern provinces, and Hebei industrial areas, to the measurement sites. Air pollution control measures during the APEC Conference significantly reduced BC at the conference site (Huairou) and in Central Beijing, with greater reductions in BC concentrations at the conference site than in Central Beijing. The highest BC concentrations in Huairou were associated with air masses originating from Central Beijing rather than from the Hebei industrial region. The success of the control measures implemented in Beijing and the surrounding regions demonstrates that BC concentrations can be effectively reduced to protect human health and mitigate regional climate forcing. This study also demonstrates the need for regional strategies to reduce BC concentrations, since urban areas like Beijing are sources as well as downwind receptors of emissions.

The Kuril Islands region is considered promising for development of salmon aquaculture. There are 41 salmon fish hatcheries in the Sakhalin Island and the Kuril Islands, 34 of them are hatcheries of the chum. Therefore, concentrations of six elements (Zn, Cu, Cd, Pb, As, and Hg) were determined in chum salmon were caught in this region. The contents of toxic elements (Cd, Pb, As, and Hg) don't exceed their maximum permissible concentrations (MPC) according to the Russian sanitary standards, but concentration of Pb are closely to MPC. Increased concentrations of Pb in wild chum have the natural origin. The unusual conditions of the Western Pacific are formed under the influence such factors as volcanism and upwelling.

Vast areas of Europe were contaminated by the fallout of ¹³⁷Cs and other radionuclides, as a result of the Chernobyl accident in 1986. The post-fallout redistribution of Chernobyl-derived ¹³⁷Cs was associated with erosion and sediment transport processes within the fluvial system. Bottom sediments from lakes and reservoirs can provide a valuable source of information regarding the post-fallout redistribution and fate of ¹³⁷Cs released by the Chernobyl accident. A detailed investigation of sediment-associated ¹³⁷Cs in the bottom sediments of a reservoir in a Chernobyl-affected area in Central Russia has been undertaken. A new approach, based on the vertical distribution of ¹³⁷Cs activity concentrations in the reservoir bottom sediment makes it possible to separate the initially deposited bottom sediment, where the ¹³⁷Cs activity reflects the direct fallout of Chernobyl-derived ¹³⁷Cs to the reservoir surface and its subsequent incorporation into sediment deposited immediately after the accident, from the sediment mobilized from the catchment deposited subsequently. The deposits representing direct fallout from the atmosphere was termed the “Chernobyl peak”. Its shape can be described by a diffusion equation and it can be distinguished from the remaining catchment-derived ¹³⁷Cs associated with sediment accumulated with sediments during the post-Chernobyl period. The ¹³⁷Cs depth distribution above the "Chernobyl peak" was used to provide a record of changes in the concentration of sediment-associated ¹³⁷Cs transported from the upstream catchment during the post-Chernobyl period. It was found that the ¹³⁷Cs activity concentration in the sediment deposited in the reservoir progressively decreased during the 30-year period after the accident due to a reduction in the contribution of sediment eroded from the arable land in the catchment. This reflects a reduction in both the area of cultivated land area and the reduced incidence of surface runoff from the slopes during spring snowmelt due to climate warming.

We investigated the profiles and levels of perfluoroalkyl carboxylic acid (PFCA) contamination in Pacific cod (Gadus macrocephalus) from the North Pacific Ocean. The mean concentrations of PFCAs containing 8 to 14 carbon atoms (C8–C14) in edible Pacific cod muscle ranged from 216 to 670 pg g⁻¹ wet weight in the Northeast Pacific Ocean (Seattle, Vancouver, Alaska, and Russia), from 819 to 1710 pg g⁻¹ wet weight in Japanese coastal waters (Hokkaido, Aomori, Iwate, Miyagi, Tottori, and Shimane), and from 288 to 892 pg g⁻¹ wet weight in Korean waters (Sokcho, Busan, and Yeosu). These results indicate there are geographical differences in the distribution of PFCAs. The long-chain PFCAs (C9–C14) contributed 96% of the total PFCA concentration across Japan, whereas they contributed only 33% of the total PFCA concentration in the USA and Canada. Long-chain PFCA concentrations in cod samples collected in Japanese and Korean waters were about three to four times those in samples from the USA, Canada, and Russia. Because seafood is considered an important dietary source of PFCAs, high concentrations of long-chain PFCAs in Pacific cod from Japanese and Korean waters may affect human dietary exposure and blood concentrations of long-chain PFCAs.

During the last 70 years 1, 2, 3, 4, 5, 6-Hexachlorocyclohexane (HCH) has been one of the most extensively used pesticides. Only the gamma-isomer has insecticidal properties. For the marketing of gamma-HCH (lindane) the other 85% HCH isomers which are formed as by-products during HCH production had to be separated and became finally hazardous waste. For each tonne of lindane 8–12 tonnes of waste HCH isomers were produced and production of the approximately 600,000 t of lindane has therefore generated 4.8 to 7.2 million tonnes of HCH/POPs waste. These waste isomers were mostly buried in uncontrolled dumps at many sites around the world. The stockpiles and the large contaminated sites can be categorized as “mega-sites”. Countries with HCH legacy problems include Albania, Argentina, Austria, Azerbaijan, Brazil, China, Croatia, Czech Republic, France, Germany, Hungary, India, Italy, Japan, Macedonia, Nigeria, Poland, Romania, Russia, Slovakia, South Africa, Spain, Switzerland, Turkey, The Netherlands, UK, Ukraine and the USA.As lindane and alpha- and beta-HCH have been listed as POPs in the Stockholm Convention since August 2010, the problem of stockpiles of HCH waste is now documented and globally acknowledged.This article describes briefly the legacy of HCH and lindane that has been created. Three of the mega-sites are being discussed and demonstrate the increase in pollution footprint over time. Recent developments in the EU (including the Sabinanigo project in Aragon/Spain) and on a global level are presented. A short overview is given on lack of activities and on actions of countries within their obligations as Parties of the Stockholm Convention. Furthermore, current country activities supported by the Global Environment Facility (GEF), the “financing mechanism” of the convention, are listed. Finally, conclusions and recommendations are formulated that will contribute to the solution of this problem over the next 25 years.

PM2.5 pollution is threatening human health and quality of life, especially in some densely populated regions of Asia and Africa. This paper used remotely sensed annual mean PM2.5 concentrations to explore the spatiotemporal evolution of global continental PM2.5 pollution from 2000 to 2014. The work employed an improved Bayesian space-time hierarchy model combined with a multiscale homogeneous subdivision method. The statistical results quantitatively demonstrated a ‘high-value increasing and low-value decreasing’ trend. Areas with annual PM2.5 concentrations of more than 70μg/m3 and less than 10μg/m3 expanded, while areas with of an annual PM2.5 concentrations of 10–25μg/m3 shrank. The most heavily PM2.5-polluted areas were located in northwest Africa, where the PM2.5 pollution level was 12.0 times higher than the average global continental level; parts of China represented the second most PM2.5-polluted areas, followed by northern India and Saudi Arabia and Iraq in the Middle East region. Nearly all (96.50%) of the highly PM2.5-polluted area (hot spots) had an increasing local trend, while 68.98% of the lightly PM2.5-polluted areas (cold spots) had a decreasing local trend. In contrast, 22.82% of the cold spot areas exhibited an increasing local trend. Moreover, the spatiotemporal variation in the health risk from exposure to PM2.5 over the global continents was also investigated. Four areas, India, eastern and southern China, western Africa and central Europe, had high health risks from PM2.5 exposure. Northern India, northeastern Pakistan, and mid-eastern China had not only the highest risk but also a significant increasing trend; the areas of high PM2.5 pollution risk are thus expanding, and the number of affected people is increasing. Northern and central Africa, the Arabian Peninsula, the Middle East, western Russia and central Europe also exhibited increasing PM2.5 pollution health risks.

Environmental pollution, local climatic conditions and their association with the prevalence and exacerbation of asthma are topics of intense current medical investigation.Air pollution in the area of Vladivostock was estimated both by the index of emission volumes of "air gaseous components" (nitrogen oxide and nitrogen dioxide, formaldehyde, hydrogen sulfide, carbon monoxide) in urban atmosphere and by mass spectrometric analysis of precipitates in snow samples. A total of 172 local asthma patients (101 controlled-asthma patients–CAP and 71 non-controlled asthma patients – nCAP) were evaluated with the use of spirometry and body plethysmography. Airway obstruction reversibility was evaluated with the use of an inhaled bronchodilator. Using discriminant analysis the association of environmental parameters with clinical indices of asthma patients is explored and thresholds of impact are established.CAP presented high sensitivity to large-size suspended air particles and to several of the studied climatic parameters. Discriminant analysis showed high values of Wilks’ lambda index (α = 0.69–0.81), which implies limited influence of environmental factors on the respiratory parameters of CAP. nCAP were more sensitive and susceptible to the majority of the environmental factors studied, including air suspended toxic metals particles (Cr, Zn and Ni). Air suspended particles showed higher tendency for pathogenicity in nCAP population than in the CAP, with a wider range of particle sizes being involved. Dust fractions ranging from 0 to 1 μm and from 50 to 100 μm were additionally implicated compared to CAP group. Considerably lowest thresholds levels of impact are calculated for nCAP.

In the summer of 2010, more than 6 hundred wildfires broke out in western Russia because of an unprecedented intense heat wave that resulted from strong atmospheric blocking. The present study evaluated the CO2 emissions using GOSAT (Greenhouse gases Observing SATellite) data from July 23 to August 18, 2010 for western Russia. The results demonstrated that the GOSAT CAI (Cloud and Aerosol Imager) was well-suited for the identification of smoke plumes and that the GOSAT FTS (Fourier-Transform Spectrometer) TIR (Thermal InfraRed) could be used to calculate the height of the plumes at approximately 800 hPa (1.58 km). Using GOSAT data, we estimated that the 2010 fires in western Russia emitted 255.76 Tg CO2. We also calculated the CO2 emissions by employing the Biomass Burning Model (BBM) for the same study site and obtained a similar result of 261.82–302.48 Tg CO2. The present study proposes a new method for the evaluation of CO2 emissions from a wildfire using remote sensing data, which could be used to improve the knowledge of the burning of biomass at a regional or a continental scale, to reduce the uncertainties in modeling greenhouse gases emissions, and to further understand how wildfires impact the atmospheric carbon cycle and global warming.

The purpose of this study was to investigate the levels of polychlorinated biphenyl (PCB), phthalic acid esters (PAE), polycyclic aromatic hydrocarbons (PAH) and organochlorine substances (OCP) in the Moscow River water. Some studies have reported the occurrence of these substances in the soil of the Moscow region; however, no study has yet established an overview for these compounds in the Moscow River water. In this study the Moscow River water contamination with PAEs, PAHs and OCPs was determined. Obtained results were associated with the resident area located on the river bank, and the possible contamination sources were considered. The obtained data were compared with the data on the contamination of the different world-wide rivers. This research indicates the further study necessity of the Moscow region to cover more contaminated sites and environmental compartments.