The measurements of dew formation efficiency and chemistry were performed in Poland in September 2009, as a part of a longer, two-year sampling campaign. Pairs of sites, representing centers of major Polish cities and rural conditions in three different regions, were compared. With the aim to get more detailed landuse-oriented characteristics of dew, two additional sites were set close to Wroclaw. Collection of dew at each site was made by means of flat, insulated, passive radiative condenser, 1 m2 in area. The analysis has included a number of physico-chemical variables, i.e.: dew water volume, pH, conductivity (σ), concentration of some major anions: F−, Cl−, NO2−, NO3−, SO42−, PO43− and cations: Na+, K+, Mg2+, Ca2+, NH4+. The dew formation efficiency at the rural stations is about two times higher than in the nearby city centres and such regularity is complex in its origin. The results show generally low contamination of dew (16.8–132.6 μS cm−1) in comparison to literature examples, but definitely more acidic (pH ∼5.0). The urban dew is characterized about two times higher contamination than nearby rural and independently of the place of collection the dominant ions are NO3−, SO42− and Ca2+, all anthropogenic in origin. The sources of dew pollution have mostly regional character or alternatively urban emissions effectively contaminate dew even several tens of kilometers away. The urban dew pH is higher than rural, but dew is potentially acidic and corrosive at the level of urban canopy.

Two primary schools and one kindergarten were selected in the city of Kozani, Greece in order to investigate the school environment, the indoor air pollutants that children are exposed to and possible health risks at school. In each school three classrooms and one outdoor position were monitored from Monday to Friday, in both non-heating (26/09/2011–14/10/2011) and heating (23/01/2012–10/02/2012) period. Temperature, relative humidity and CO2, were continuously monitored. Formaldehyde, benzene, trichloroethylene, pinene, limonene, NO2 and O3 were measured with diffusive samplers. CO was monitored every day (30 min/day). Radon was measured for four weeks with short term radon detectors. PM2.5 was gravimetrically determined while PM2.5 and PM10 fractions were measured using the optical light scattering technique. Building material emission testing for VOCs was performed using the Field and Laboratory Emission Cell (FLEC). The ventilation rate for each classroom was calculated based on the CO2 measurements.Results indicated that indoor air concentrations of the measured pollutants were within accepted limits with indicative ranges 1.5–9.4 μg/m3 for benzene, 2.3–28.5 μg/m3 for formaldehyde, 4.6–43 μg/m3 for NO2 and 0.1–15.6 μg/m3 for O3. Emissions from building materials seem to have a significant contribution to the indoor air quality. Very low ventilation rates (0.1–3.7 L/s per person) were observed, indicating inadequate ventilation and possible indoor air quality problems requiring intervention measures. The estimated average lifetime cancer risks for benzene, formaldehyde and trichloroethylene were very low.

PM2.5 and PM10 samples were collected in a rural area from December 2014 to August 2015 near a coal-fired power plant on the southeast coast of China. The total mercury concentrations in PM2.5 ranged from 116.2 to 1070.9 pg/m3 and in PM10 from 173.4 to 1456.8 pg/m3, with averages of 309.5 ± 94.9 and 387.5 ± 133.5 pg/m3, respectively. These were much higher than those found in many foreign cities. The concentrations of mercury in PM2.5 and PM10 varied seasonally, with the highest average concentration in winter. This was probably due to the seasonal variation of meteorological conditions and concentration of particulates. The highest mass-based concentration of mercury in PM2.5 and PM10 was observed in spring. This result might be related to the prevailing sea winds in spring. The spatial variation of particulate mercury conformed to the concentration distribution characteristics of pollutant discharged from coal-fired power plant elevated source at the downwind area. The seasonal variation in the concentrations of the four mercury species (including exchangeable particulate mercury: EXPM, HCl-soluble particulate mercury: HPM, elemental particulate mercury: EPM, and residual particulate mercury: RPM) were all identical to the seasonal variation of total particulate mercury (TPM) in PM2.5 and PM10 (winter > spring > summer). Owing to the variation of meteorological conditions, the proportion of different mercury species in TPM followed different seasonal trends. In contrast to RPM, the percentage of both HPM and EPM in PM2.5 was higher than in PM10.

Spatial distributions and temporal variations of trace metals in Korean coastal sediments were investigated by determining seven metals (As, Cd, Cr, Cu, Hg, Pb, and Zn) in sediment collected from 71 stations between 2004 and 2010 (n=491). High metal concentrations were found in the southeastern coast, where there are many cities and industrial complexes, indicating that metal concentrations in Korean coastal sediment are significantly influenced by human activities associated with urbanization and industrialization. However, metal concentrations in sediment did not markedly vary temporally, which was because the coast is managed sustainably and because of the characteristics of the sediment environments. Based on the sediment quality guidelines and geoaccumulation index, Korean coastal sediments are practically unpolluted with Cd, Cr, Cu, Hg, Pb and Zn but moderately polluted with As. More intensive monitoring is required to determine the potential As sources and to understand the As geochemical cycles in Korean coastal sediments.

In this work, a hydrocarbon-degrading bacterium Y-1 isolated from petroleum contaminated soil in the Dagang Oilfield was investigated for its potential effect in biodegradation of crude oil. According to the analysis of 16S rRNA sequences, strain Y-1 was identified as Bacillus licheniformis. The growth parameters such as pH, temperature, and salinity were optimised and 60.2% degradation of crude oil removal was observed in 5days. The strain Y-1 showed strong tolerance to high salinity, alkalinity, and temperature. Emplastic produced by strain Y-1 at high temperatures could be applied as biosurfactant. Gas chromatography analysis demonstrated that the strain Y-1 efficiently degraded different alkanes from crude oil, and the emplastic produced by strain Y-1 promoted the degradation rates of long-chain alkanes when the temperature increased to 55°C. Therefore, strain Y-1 would play an important role in the area of crude oil contaminant bioremediation even in some extreme conditions.

We inserted 190 FTIR spectra of plastic samples in a digital database and submitted it to Independent Component Analysis (ICA) to extract the “pure” plastic polymers present. These identified plastics were polypropylene (PP), high density polyethylene (HDPE), low density polyethylene (LDPE), high density polyethylene terephthalate (HDPET), low density polyethylene terephthalate (LDPET), polystyrene (PS), Nylon (NL), polyethylene oxide (OPE), and Teflon (TEF) and they were used to establish the similarity with unknown plastics using the correlation coefficient (r), and the crosscorrelation function (CC). For samples with r<0.8 we determined the Mahalanobis Distance (MD) as additional tool of identification. For instance, for the four plastic fragments found in the Carretta carretta, one plastic sample was assigned to OPE due to its r=0.87; for all the other three plastic samples, due to the r values ranging between 0.83 and0.70, the support of MD suggested LDPET and OPE as co-polymer constituents.

Rare earth elements (REE) are a homogenous group of 17 chemical elements in the periodic table that are key to many modern industries including chemicals, consumer electronics, clean energy, transportation, health care, aviation, and defense. Moreover, in recent years, they have been used in agriculture. One of the consequences of their worldwide use is the possible increase of their levels in various environmental compartments. This review addresses major topics concerning the study of REE in the soil environment, with special attention to the latest research findings. The main sources of REE to soils, the contents of REE in soils worldwide, and relevant information on the effects of REE to plants were explored. Ecological and human health risk issues related to the presence of REE in soils were also discussed. Although several findings reported positive effects of REE on plant growth, many questions about their biological role remain unanswered. Therefore, studies concerning the actual mechanism of action of these elements on cellular and physiological processes should be further refined. Even more urgent is to unveil their chemical behavior in soils and the ecological and human health risks that might be associated with the widespread use of REE in our modern society.

The elevated concentration of arsenic (As) in the groundwaters of many countries worldwide has received much attention during recent decades. This article presents an overview of the natural geochemical processes that mobilize As from aquifer sediments into groundwater and provides a concise description of the distribution of As in different global groundwater systems, with an emphasis on the highly vulnerable regions of Southeast Asia, the USA, Latin America, and Europe. Natural biogeochemical processes and anthropogenic activities may lead to the contamination of groundwaters by increased As concentrations. The primary source of As in groundwater is predominantly natural (geogenic) and mobilized through complex biogeochemical interactions within various aquifer solids and water. Sulfide minerals such as arsenopyrite and As-substituted pyrite, as well as other sulfide minerals, are susceptible to oxidation in the near-surface environment and quantitatively release significant quantities of As in the sediments. The geochemistry of As generally is a function of its multiple oxidation states, speciation, and redox transformation. The reductive dissolution of As-bearing Fe(III) oxides and sulfide oxidation are the most common and significant geochemical triggers that release As from aquifer sediments into groundwaters. The mobilization of As in groundwater is controlled by adsorption onto metal oxyhydroxides and clay minerals. According to recent estimates, more than 130 million people worldwide potentially are exposed to As in drinking water at levels above the World Health Organization’s (WHO's) guideline value of 10 μg/L. Hence, community education to strengthen public awareness, the involvement and capacity building of local stakeholders in targeting As-safe aquifers, and direct action and implementation of best practices in identifying safe groundwater sources for the installation of safe drinking water wells through action and enforcement by local governments and international water sector professionals are urgent necessities for sustainable As mitigation on a global scale.

This study reviews recent research on volatile organic compound (VOC) emissions from motorized vehicle sources by means of online mass spectrometry. Chemical ionization is a powerful tool that usually permits soft ionization of chemical species and it allows the time-resolved measurement of multiple VOCs, even in complex samples where many kinds of VOCs coexist. The vehicular exhaust gasses are investigated using H₃O⁺, NO⁺, Hg⁺, and CH₃C(O)O⁻ as a reagent ion in online chemical ionization mass spectrometry. The proton transfer using H₃O⁺ as a reagent ion was used for the detection of nitro-organic compounds such as nitromethane and nitrophenol. The time-resolved measurement of the nitro-organic compounds in the laboratory experiments with a chassis dynamometer system revealed their emission properties, such as the dependence of the emissions as a function of vehicular velocity and acceleration/deceleration, as well as the effect of various types of exhaust gas treatment. The data regarding the nitromethane and nitrophenol emissions obtained in the field measurements were consistent with the results of the laboratory experiments done with a chassis dynamometer system. In the experiments involving evaporative emissions from gasoline-powered cars, NO⁺ was used as a reagent ion. Online measurements showed that the adsorption of hydrocarbons in a sealed housing evaporative determination unit could result in emissions being underestimated, if the concentrations are monitored only before and after a diurnal breathing loss test. The composition analysis gave an estimated ozone formation potential (OFP) approximately 20 % higher for breakthrough emissions and refueling emissions than for the gasoline that was tested, but the OFP for the permeation emissions was almost the same as the OFP for the test fuel.

Reliable assessment of water quality is a critical issue for estuaries. Nutrient concentrations show significant spatial distinctions between areas under the influence of fresh-sea water interaction and anthropogenic effects. For this situation, given the limitations of general mean estimation approaches, a new method for surfaces with non-homogeneity (MSN) was applied to obtain optimized linear unbiased estimations of the mean nutrient concentrations in the study area in the Yangtze estuary from 2011 to 2013. Other mean estimation methods, including block Kriging (BK), simple random sampling (SS) and stratified sampling (ST) inference, were applied simultaneously for comparison. Their performance was evaluated by estimation error. The results show that MSN had the highest accuracy, while SS had the highest estimation error. ST and BK were intermediate in terms of their performance. Thus, MSN is an appropriate method that can be adopted to reduce the uncertainty of mean pollutant estimation in estuaries.