Chicken organs, animal feed, droppings, and ambient air were sampled at a farm in Beijing to determine the concentrations of hexachlorocyclohexane isomers (HCHs) and dichlorodiphenyltrichloroethane and metabolites (DDTs). Mean fresh weight concentrations of HCHs and DDTs were 0.122 ± 0.061 ng/g and 0.051 ± 0.038 ng/g in the muscles. These values are 1-2 orders of magnitude lower than those reported in China in 1980. Contaminated feed was the main source of HCHs and DDTs. Only 12.8% of HCH and 3.3% of DDT of the amount consumed were excreted. Accumulated quantities of HCHs and DDTs increased during growth. However, concentrations of HCHs and DDTs did not increase because of dilution from rapid growth. Based on the observed residual levels in mature chicken and the average diet of residents of China, the contributions from chicken and egg consumption to per capita daily intake of HCHs and DDTs were 487% and 88% of those of fish consumption.

A biomonitoring network with leafy vegetables was established near a chlor-alkali plant in order to compare the accumulation of mercury to the atmospheric total gaseous mercury (TGM) concentration. Based on data obtained in the reference area the 'normal' mercury concentration in vegetables is between 0.6 and 5.4 μg kg⁻¹ FW. The effect detection limits (EDLs) are between 1.2 and 11.0 μg kg⁻¹ FW and the biological detection limits (BDLs), the lowest [TGM] that can be detected significantly, are between 3 and 4 ng m⁻³. The accumulation rate is lowest for lettuce and high for curly kale that proved to be an excellent accumulator and as such it is very useful for biomonitoring purposes. A comparison made in the 1980s between biomonitoring results with grass and the mercury concentration in leafy vegetables from private gardens nearby proved to be valid when applied to the current biomonitoring results with vegetables. Leafy vegetables are an important component in the transfer of atmospheric mercury through the terrestrial food chain.

The troposphere is subject to continuous inputs, production and removal processes of ozone and its precursors from natural processes and human activities acting together within a very complex system. In order to assess the behaviour of background ozone in the Mediterranean area, a description of trends, seasonal and diurnal behaviours of free tropospheric ozone is provided. In the Mediterranean area and southern Europe the background tropospheric ozone concentration appears significantly affected by three main air mass transport processes: (i) transport of polluted air masses on regional and long-range scales, (ii) downward transport of stratospheric air masses, and (iii) transport of mineral dust from the Sahara desert. In this review of the literature of the last two decades, we present an overview of these phenomena, mainly monitored at high baseline mountain stations representative of background atmospheric conditions. How background ozone is influenced by vertical and horizontal transport processes in the southern Europe and the Mediterranean area.

Chlorobenzene-contaminated groundwater was used to assess pulsed gas sparging as a minimum effort aeration strategy to enhance intrinsic natural attenuation. In contrast to existing biosparging operations, oxygen was supplied at minimum rate by reducing the gas injection frequency to 0.33 day⁻¹. Field tests in a model aquifer were conducted in a 12 m long reactor, filled with indigenous aquifer material and continuously recharged with polluted groundwater over 3 years. The closed arrangement allowed yield balances, cost accounting as well as the investigation of spatial distributions of parameters which are sensitive to the biodegradation process. Depending on the injection frequency and on the gas chosen for injection (pure oxygen or air) oxygen-deficient conditions prevailed in the aquifer. Despite the limiting availability of dissolved oxygen in the groundwater, chlorobenzene degradation under oxygen-deficient conditions proved to be more effective than under conditions with dissolved oxygen being available in high concentrations. Minimum rate gas sparging resulted in sustained biodegradation of chlorobenzene in a polluted groundwater aquifer.

Emission data needed as input for the operation of atmospheric models should not only be spatially and temporally resolved. Another important feature is the effective emission height which significantly influences modelled concentration values. Unfortunately this information, which is especially relevant for large point sources, is usually not available and simple assumptions are often used in atmospheric models. As a contribution to improve knowledge on emission heights this paper provides typical default values for the driving parameters stack height and flue gas temperature, velocity and flow rate for different industrial sources. The results were derived from an analysis of the probably most comprehensive database of real-world stack information existing in Europe based on German industrial data. A bottom-up calculation of effective emission heights applying equations used for Gaussian dispersion models shows significant differences depending on source and air pollutant and compared to approaches currently used for atmospheric transport modelling.

Mean hexachlorobenzene (HCB) and hexachlorocyclohexane (HCH) concentrations, measured in seawater and air samples, confirmed the decline in levels of these compounds in Antarctic air and water. However, low α/γ-HCH ratios in air at the beginning of the sampling period suggest a predominance of fresh lindane entering the Antarctic atmosphere during the Austral spring probably due to current use in the Southern Hemisphere. Water-air fugacity ratios demonstrate the potential for HCH gas deposition to coastal Antarctic seas, while the water-air fugacity ratios for HCB imply that volatilization does not account for the observed decrease of HCB in surface seawater. HCH concentrations found in krill samples were correlated with seawater concentrations indicative of bioconcentration of HCHs from seawater. Hexachlorocyclohexanes (HCHs) continue to decline in Antarctic air, but fugacity ratios demonstrate that Antarctic coastal waters remain a sink for HCHs, which bioconcentrate in krill via direct uptake from water.

The constructions of Cultural and Architecture Patrimony are influenced by pollutants. Many of degenerative processes in the materials which constitute them have their origin in pollutants. That is the reason why a physical-chemical characterisation of the particulate pollutants in the air has been carried out. The deposition and, as a consequence of that, the interaction of the pollutants with the different materials of the monuments depend on the reactivity of the chemical elements that form the atmospheric particulate. Studies of both, bulk dust deposition and total suspended matter, a mineralogical and chemical characterisation of them have been made. Lastly, starting from these data, it can be established that the interactions and degenerative processes are taking place in the monuments of the studied locations. In the present work, the methodology carried out in the study of the particulate atmospheric pollutants, which are capable of accumulating on monuments and buildings with artistic and historical interest in the area of Castellon, is displayed. By means of a network of captors, important samples of sedimentary and suspension atmospheric pollutants, total suspension particles (TSP) were obtained. Firstly, by gravimetric methods, we have obtained the concentration levels of these kinds of pollutants in milligrams per day in busk dust samples and micrograms per cubic meter in TSP. Due to the fact that the corrosivity of these pollutants fundamentally depends on their compositions, the study has been completed with a mineralogical and chemical characterisation. By X-ray diffraction and scanning electron microscopy, we have analysed the particles of the two kinds of samples. The chemical analysis was carried out by inductively coupled plasma-atomic spectroscopy and inductively coupled plasma-mass spectrometry (multielement analysis techniques) in TSP samples and in the soluble fraction of the depositing particulate matter. The results have shown as main compounds: clay minerals, calcite, and carbonaceous matter coming from non-perfect combustion of vehicles. The chemical analysis indicates a high Ca/S ratio and high levels of concentration in chemical elements associated to this representative industrial cluster of ceramics industry in Europe.

The use of inks containing organic solvents by the offset printing process implies in the release of volatile organic compounds to the work environment. Many of these compounds such as benzene, toluene, ethylbenzene, and the xylene isomers (well known by the acronym BTEX) are extremely toxic. In this study, the BTEX concentrations were determined in two different printing plants that use distinct types of inks: the conventional and the so-called ecological, which is manufactured based on vegetal oil. Concentration ranges were 43-84, 15-3,480, 2-133, 5-459, and 2-236 μg m⁻³ for benzene, toluene, ethylbenzene, m + p-xylene, and o-xylene, respectively, for the conventional printing plant. At the ecological printing plant, concentration ranges were below limit of detection (<LD)-31, <LD-618, <LD-1,690, <LD-10,500, <LD-3,360 μg m⁻³ for benzene, toluene, ethylbenzene, m + p-xylene, and o-xylene, respectively. BTEX concentrations are lower at the ecological printing environment than in the conventional, where mineral oil-based inks are used. However, the worker who cleans the printing matrices is exposed to high concentrations of ethylbenzene and xylenes, due probably to the cleaning product's composition (containing high amounts of BTEX). Although the BTEX concentrations found in both printing work environments were below the limits considered by the Brazilian Law for Activities and Unhealthy Operations (NR-15), the exposure to such vapors characterizes risk to the workers' health for some of the evaluated samples, mainly the personal ones.

Municipal solid waste (MSW) source-classified collection represents an advancement in resource recycling and secondary pollution control in China. Comparative experiments were performed to assess the effect of a newly-established MSW source-classified collection system on polycyclic aromatic hydrocarbons (PAHs) in bottom ash from an incinerator (BA), fly ash from a boiler (FAB) and fly ash from a bag filter (FABF) of a full-scale MSW incinerator in China. Compared with FAB or FABF, PAHs were mainly concentrated in BA with a range of 1,961.0-2,420.2 μg/kg. Total amounts of 16 high priority PAHs in BA, FAB and FABF from the classified MSW incineration were significantly reduced by 19.0%, 42.4% and 59.8% respectively in comparison with those from the traditional mixed MSW incineration. Moreover, the toxic equivalent quantity (B[a]Peq) of carcinogenic PAHs in these three kinds of residues from the classified MSW incineration were significantly decreased, with the maximum decrease observed in FABF. As a result of source-classification with effective presorting and dewatering, plastics and metals in the MSW were lower, but combustibles and heat values of the MSW increased. Due to variations of the characteristics of the feed waste, complete combustion conditions including continuous higher incineration temperature, lower CO concentration and higher air excess ratio were observed during the process of classified MSW incineration. Incineration temperature and CO concentration showed a negative and positive correlation, respectively, with total PAHs, indicating that incomplete combustion products such as PAHs could be reduced by controlling combustion conditions directly related to properties of the feed waste. The newly established MSW source-classified collection process could be a feasible method for reducing PAHs formation and emission in residues from MSW incineration.

The radiation dose and environmental health risk of radon concentration in the Lantian karst cave of China to guides and visitors were estimated based on the continuous radon concentration monitoring. Distinct seasonal variations were observed in the radon concentration of the air inside the cave. The maximum concentration occurred in the summer, whereas the minimum radon concentration occurred during the winter. The annual average radon concentration in the caves investigated is slightly higher than the upper bound of radon action level for underground space used in China and less than the upper bound of radon action level recommended by the International Commission on Radiation Protection (ICRP) for workplaces. The annual effective dose to tour guides working in two investigated caves varies from 4.1 to 16.5mSv, depending on different equilibrium factors together with different dose conversion factors proposed in the literature. The annual maximum time that a tour guide or other worker can safely be inside the cave is estimated to be 1,250 or 2,246h, depending on whether one bases this on the high or mean radon concentration, with an equilibrium factor of one in both cases. Given the synergistic effects of smoking, tour guides who are smokers should be in the cave only 10-20% of these hours. In all cases, the annual effective doses to visitors are well below the 1mSv maximum suggested dose for a member of the public for 1 year.