Characterization of ²⁴¹ Am and ¹³⁴Cs bioaccumulation in the king scallop Pecten maximus: investigation via three exposure pathways

In order to understand the bioaccumulation of ²⁴¹Am and ¹³⁴Cs in scallops living in sediments, the uptake and depuration kinetics of these two elements were investigated in the king scallop Pecten maximus exposed via seawater, food, or sediment under laboratory conditions. Generally, ²⁴¹Am accumulation was higher and its retention was stronger than ¹³⁴Cs. This was especially obvious when considering whole animals exposed through seawater with whole-body concentration factors (CF_7d) of 62 vs. 1, absorption efficiencies (A_0l) of 78 vs. 45 for seawater and biological half-lives (T_b½l) of 892 d vs. 22 d for ²⁴¹Am and ¹³⁴Cs, respectively. In contrast, following a single feeding with radiolabelled phytoplankton, the assimilation efficiency (AE) and T_b½l of ¹³⁴Cs were higher than those of ²⁴¹Am (AE: 28% vs. 20%; T_b½l: 14 d vs. 9 d). Among scallop tissues, the shells always contained the higher proportion of the total body burden of ²⁴¹Am whatever the exposure pathway. In contrast, the whole soft parts presented the major fraction of whole-body burden of ¹³⁴Cs, which was generally associated with muscular tissues. Our results showed that the two radionuclides have contrasting behaviors in scallops, in relation to their physico-chemical properties.     

Derivation of hazardous doses for amphibians acutely exposed to ionising radiation

Derivation of effect benchmark values for each taxonomic group, which has been difficult due to lack of experimental effects data, is required for more adequate protection of the environment from ionising radiation. Estimation of effects doses from nuclear DNA mass and subsequent species sensitivity distribution (SSD) analysis were proposed as a method for such a derivation in acute irradiation situations for assumed nuclear accident scenarios. As a case study, 5% hazardous doses (HD₅s), at which only 5% of species are acutely affected at 50% or higher lethality, were estimated on a global scale. After nuclear DNA mass data were obtained from a database, 50% lethal doses (LD₅₀s) for 4.8 and 36% of the global Anura and Caudata species, respectively, were estimated by correlative equations between nuclear DNA mass and LD₅₀s. Differences between estimated and experimental LD₅₀s were within a factor of three. The HD₅s obtained by the SSD analysis of these estimated LD₅₀s data were 5.0 and 3.1 Gy for Anura and Caudata, respectively. This approach was also applied to the derivation of regional HD₅s. The respective HD₅s were 6.5 and 3.2 Gy for Anura and Caudata inhabiting Japan. This HD₅ value for the Japanese Anura was significantly higher than the global value, while Caudata had no significant difference in global and Japanese HD₅s. These results suggest that this approach is also useful for derivation of regional benchmark values, some of which are likely different from the global values.     

Greenhouse gas emissions from a semi-arid tropical reservoir in northeastern Brazil

We estimated carbon dioxide (CO₂) and methane (CH₄) emissions by diffusion, ebullition, and degassing in turbines from a semi-arid hydropower reservoir in northeastern Brazil. Sampling sites were allocated within the littoral and deeper waters of one embayment, the main-stream, and at turbines. Annual carbon emissions were estimated at 2.3?×?10⁵?±?7.45?×?10⁴ t C year^?1, or in CO₂-equivalents (CO₂-eq) at 1.33?×?10⁶?±?4.5?×?10⁵ t CO₂-eq year^?1. Diffusion across the water surface was the main pathway accounting for 96% of total carbon emissions. Ebullition was limited to littoral areas. A slight accumulation of CO₂, but not of CH₄, in bottom waters close to the turbines inlet led to degassing emissions about 8?×?10³ t C year^?1. Emissions in littoral areas were higher than in main-stream and contribute to 40% of the total carbon. Carbon (C) emissions per electricity generated, at 60% of installed capacity, is 0.05 t C-CO₂-eq MWh^?1. The ratio increases to 0.09 t C-CO₂ MWh^?1, equating 80% of the emissions from natural gas and 40% of diesel or coal power plants. Retention time and benthic metabolism were identified as main drivers for carbon emissions in littoral areas, while water column mixing and rapid water flow are important factors preventing CH₄ accumulation and loss by degassing. Our results indicate that Itaparica Reservoir, located in the semi-arid region of Northeastern Brazil, acts as a source of GHGs. Management measurements are needed to prevent emissions to raise in the future.     

Characteristics of PM10, PM2.5, CO2 and CO monitored in interiors and platforms of subway train in Seoul, Korea

This study was performed to investigate the concentration of PM₁₀ and PM_2.5 inside trains and platforms on subway lines 1, 2, 4 and 5 in Seoul, KOREA. PM₁₀, PM_2.5, carbon dioxide (CO₂) and carbon monoxide (CO) were monitored using real-time monitoring instruments in the afternoons (between 13:00 and 16:00). The concentrations of PM₁₀ and PM_2.5 inside trains were significantly higher than those measured on platforms and in ambient air reported by the Korea Ministry of Environment (Korea MOE). This study found that PM₁₀ levels inside subway lines 1, 2 and 4 exceeded the Korea indoor air quality (Korea IAQ) standard of 150 μg/m³. The average percentage that exceeded the PM₁₀ standard was 83.3% on line 1, 37.9% on line 2 and 63.1% on line 4, respectively. PM_2.5 concentration ranged from 77.7 μg/m³ to 158.2 μg/m³, which were found to be much higher than the ambient air PM_2.5 standard promulgated by United States Environmental Protection Agency (US-EPA) (24 h arithmetic mean: 65 μg/m³). The reason for interior PM₁₀ and PM_2.5 being higher than those on platforms is due to subway trains in Korea not having mechanical ventilation systems to supply fresh air inside the train. This assumption was supported by the CO₂ concentration results monitored in tube of subway that ranged from 1153 ppm to 3377 ppm. The percentage of PM_2.5 in PM₁₀ was 86.2% on platforms, 81.7% inside trains, 80.2% underground and 90.2% at ground track. These results indicated that fine particles (PM_2.5) accounted for most of PM₁₀ and polluted subway air. GLM statistical analysis indicated that two factors related to monitoring locations (underground and ground or inside trains and on platforms) significantly influence PM₁₀ (p < 0.001, R² = 0.230) and PM_2.5 concentrations (p < 0.001, R² = 0.172). Correlation analysis indicated that PM₁₀, PM_2.5, CO₂ and CO were significantly correlated at p < 0.01 although correlation coefficients were different. The highest coefficient was 0.884 for the relationship between PM₁₀ and PM_2.5.     

Contribution of (222)Rn-bearing water to indoor radon and indoor air quality assessment in hot spring hotels of Guangdong, China

This study investigates the contribution of radon (²²²Rn)-bearing water to indoor ²²²Rn in thermal baths. The ²²²Rn concentrations in air were monitored in the bathroom and the bedroom. Particulate matter (PM, both PM₁₀ and PM_2.5) and carbon dioxide (CO₂) were also monitored with portable analyzers. The bathrooms were supplied with hot spring water containing 66-260 kBq m⁻³ of ²²²Rn. The results show that the spray of hot spring water from the bath spouts is the dominant mechanism by which ²²²Rn is released into the air of the bathroom, and then it diffuses into the bedroom. Average ²²²Rn level was 110-410% higher in the bedrooms and 510-1200% higher in the bathrooms compared to the corresponding average levels when there was no use of hot spring water. The indoor ²²²Rn levels were influenced by the ²²²Rn concentrations in the hot spring water and the bathing times. The average ²²²Rn transfer coefficients from water to air were 6.2 × 10⁻⁴-4.1 × 10⁻³. The 24-h average levels of CO₂ and PM₁₀ in the hotel rooms were 89% and 22% higher than the present Indoor Air Quality (IAQ) standard of China. The main particle pollutant in the hotel rooms was PM_2.5. Radon and PM₁₀ levels in some hotel rooms were at much higher concentrations than guideline levels, and thus the potential health risks to tourists and especially to the hotel workers should be of great concern, and measures should be taken to lower inhalation exposure to these air pollutants.     

Occupational exposure to radon and natural gamma radiation in the La Carolina, a former gold mine in San Luis Province, Argentina

Radon and gamma radiation level measurements were carried out inside the La Carolina mine, one of the oldest gold mining camps of southern South America, which is open for touristic visits nowadays. CR-39 track-etch detectors and thermoluminescent dosimeters of natural CaF₂ and LiF TLD-100 were exposed at 14 points along the mine tunnels in order to estimate the mean ²²²Rn concentration and the ambient dose equivalent during the summer season (November 2008 to February 2009). The values for the ²²²Rn concentration at each monitoring site ranged from 1.8 ± 0.1 kBq m⁻³ to 6.0 ± 0.5 kBq m⁻³, with a mean value of 4.8 kBq m⁻³, indicating that these measurements exceed in about three times the upper action level recommended by ICRP for workplaces. The correlations between radon and gamma radiation levels inside the mine were also investigated. Effective doses due to ²²²Rn and gamma rays inside the mine were determined, resulting in negligible values to tourists. Considering the effective dose to the mine tourist guides, values exceeding 20 mSv of internal contribution to the effective doses can be reached, depending on the number of working hours inside the mine.     

Chemical characteristics of precipitation and wet deposition of major ions in Liaozhong County of Liaoning Province,Northeast China

The chemical characteristics of precipitation were analyzed based on the chemical composition of principal ionic within acid rain（from February 2007 to January 2008）of Liaozhong Meteorological Station located in Malong Village in Liaozhong County of Northeast China,meteorological conditions on the corresponding period ground,and variation of several air pollutants concentration.The results indicated that:（1）The precipitation average pH value of all samples was4.76;the frequency of acid rain during the observation period was 70.7%;the frequency was 82.8%in summer and autumn.（2）In the chemical composition of precipitation,the primary anions were SO₄^2-and NO₃^-;the primary cations were NH₄⁺and Ca²⁺.（3）All concentration of anions was higher in summer and winter,but relatively low in spring and autumn.This showed that the relationship between regional rainfall acidification and pollution was not significant.（4）Rainwater acidity and nearly floor gaseous pollution concentration were different from each other,and pH and NO_x,CO,NO₂ and O₃concentrations showed significant negative correlation,but was not obvious with SO₂ concentration.However,the pH and alkaline pollutants,such as particulate,was positively correlative.     

Actual evapotranspiration and canopy resistance measurement of the savannah in the Kouilou basin (Congo-Brazzaville)

The aim of this work is to study the actual evapotranspiration and surface resistance of the savannah using the Bowen-ratio method for two contrasted periods, dry and rainy season. The reliability of this method has been assessed by comparison with the Monteith equation and the soil-water balance method in a 90% Loudetia arundinacea dominated savannah (Pointe Noire, Congo). Our results relate to the period from 18 September to 11 October 1998 (24 days): (a) from 18 to 29 September (“dry season”), the soil-water content was less than 70% of the soil-water content at field capacity (63–70% of R _FC; large soil-water stress; T/E _P from 0.2 to 0.4); (b) from 30 September to 11 October (“rainy season”) soil-water content close to 90–92% of RFC; no soil-water stress; T/E _P from 0.73 to 0.77). The mean daily surface resistance reulting from the Bowen-ratio method was 317 s m^?1, 355 s m^?1 during the “dry season” and 279 s m^?1 during the “rainy season”. The total actual evapotranspiration (E _a) resulting from the Bowen-ratio method, Penman-Monteith equation and soil-water balance method were, respectively of 58.6–57.8 and 56.2 mm, with the mean daily E_a of 2.4–2.4 and 2.3 mm day^?1 (2.4–1.5 and 2.2 mm day^?1 in “dry season” and of 2.5–3.4 and 2.5 mm day^?1 in “rainy season”). The Bowen-ratio method was used for the assessment of the actual evapotranspiration from the temperature and specific humidity differences, net radiation and the soil heat flux measurement: its advantages are a rapidity of installation, a temporal resolution of measurement in less than one hour and a good integration of the heterogeneousness of the savannah’s latent flux of vaporization. This method is adapted to eco-physiological studies in tropical conditions with reduced teams.     

Behavior and analysis of Cesium adsorption on montmorillonite mineral

The adsorption of Cs by montmorillonite and the effects of experimental conditions on adsorption were investigated by using ¹³⁴Cs as a radioactive tracer. Additionally, the Cs-adsorbed and the modified montmorillonite were analyzed by X-ray Diffractometer System (XRD) and Scanning Electron Microscopy (SEM). The results showed that the adsorption of Cs by montmorillonite was efficient in the initial concentration (C₀) of 30 μg/L Cs nitrate solution with 20 g/L montmorillonite at room temperature. In this condition, more than 98% Cs⁺ ions could be adsorbed at pH 8. The adsorption equilibrium was achieved within 5 min and the relationship between the concentration of Cs⁺ in aqueous solutions and adsorption capacities of Cs⁺ can be described by the Langmuir adsorption isotherm. The adsorption rate would decrease when temperature increase from 0 °C to 50 °C or in presence of coexistent K⁺, Na⁺ and Ca²⁺, while modification by (NH₄)₂SO₄, [Ag(NH₃)₂]⁺, [Cu(NH₃)₄]²⁺ or 450 °C could improve the adsorption abilities of montmorillonite for Cs⁺. However, more than 89% of adsorbed Cs⁺ on montmorillonite could be desorbed by 2 mol/L HNO₃ solutions. The XRD and SEM analysis further showed that the structure of the Cs-adsorbed or modified montmorillonite were different from that of the original one.     

A quantitative integrated assessment of pollution prevention achieved by Integrated Pollution Prevention Control licensing

This paper presents an innovative, quantitative assessment of pollution avoidance attributable to environmental regulation enforced through integrated licensing, using Ireland's pharmaceutical-manufacturing sector as a case study. Emissions data reported by pharmaceutical installations were aggregated into a pollution trend using an Environmental Emissions Index (EEI) based on Lifecycle Assessment methodologies. Complete sectoral emissions data from 2001 to 2007 were extrapolated back to 1995, based on available data. Production volume data were used to derive a sectoral production index, and determine ‘no-improvement’ emission trends, whilst questionnaire responses from 20 industry representatives were used to quantify the contribution of integrated licensing to emission avoidance relative to these trends. Between 2001 and 2007, there was a 40% absolute reduction in direct pollution from 27 core installations, and 45% pollution avoidance relative to hypothetical ‘no-improvement’ pollution. It was estimated that environmental regulation avoided 20% of ‘no-improvement’ pollution, in addition to 25% avoidance under business-as-usual. For specific emissions, avoidance ranged from 14% and 30 kt a^− 1 for CO₂ to 88% and 598 t a^− 1 for SO_x. Between 1995 and 2007, there was a 59% absolute reduction in direct pollution, and 76% pollution avoidance. Pollution avoidance was dominated by reductions in emissions of VOCs, SO_x and NO_x to air, and emissions of heavy metals to water. Pollution avoidance of 35% was attributed to integrated licensing, ranging from between 8% and 2.9 t a^− 1 for phosphorus emissions to water to 49% and 3143 t a^− 1 for SO_x emissions to air. Environmental regulation enforced through integrated licensing has been the major driver of substantial pollution avoidance achieved by Ireland's pharmaceutical sector — through emission limit values associated with Best Available Techniques, emissions monitoring and reporting requirements, and performance targets specified in environmental management plans. This compliant sector offers a positive, but not necessarily typical, case study of IPPC effectiveness.     

The influence of hot particle contamination on Sr and Cs transfers to milk and on time-integrated ingestion doses

Most models for transfers of radionuclides through the food chain typically assume that the radioactivity is initially deposited in chemically available forms. It is known, however, that releases of radionuclides in the form of hot particles may significantly influence their environmental transfers and uptake to the food chain. This study presents models for time changes in ⁹⁰Sr and ¹³⁷Cs in milk which incorporate hot particle contamination using observed rates of hot particle dissolution following the Chernobyl accident. A general equation is presented for the influence of hot particles on overall ingestion doses. As expected from previous work, fallout of hot particles significantly influences time changes in radionuclide activity concentrations in foodstuffs. It is also shown that incorporation of radionuclides in hot particles influences time-integrated ingestion doses. For a situation in which a large proportion (90–100%) of fallout is in slowly dissolving hot particles, time-integrated ingestion doses from ⁹⁰Sr and ¹³⁷Cs are reduced by a factor of approximately two compared to the case where all radioactivity is deposited in bioavailable forms. However, the influence of rapidly dissolving hot particles on time-integrated ingestion doses is relatively minor. Remaining significant uncertainties in dose estimates are discussed.     

Associations between short-term exposure to nitrogen dioxide and mortality in 17 Chinese cities: The China Air Pollution and Health Effects Study (CAPES)

Few multi-city studies in Asian developing countries have examined the acute health effects of ambient nitrogen dioxide (NO₂). In the China Air Pollution and Health Effects Study (CAPES), we investigated the short-term association between NO₂ and mortality in 17 Chinese cities. We applied two-stage Bayesian hierarchical models to obtain city-specific and national average estimates for NO₂. In each city, we used Poisson regression models incorporating natural spline smoothing functions to adjust for long-term and seasonal trend of mortality, as well as other time-varying covariates. We examined the associations by age, gender and education status. We combined the individual-city estimates of the concentration–response curves to get an overall NO₂–mortality association in China. The averaged daily concentrations of NO₂ in the 17 Chinese cities ranged from 26 μg/m³ to 67 μg/m³. In the combined analysis, a 10-μg/m³ increase in two-day moving averaged NO₂ was associated with a 1.63% [95% posterior interval (PI), 1.09 to 2.17], 1.80% (95% PI, 1.00 to 2.59) and 2.52% (95% PI, 1.44 to 3.59) increase of total, cardiovascular, and respiratory mortality, respectively. These associations remained significant after adjustment for ambient particles or sulfur dioxide (SO₂). Older people appeared to be more vulnerable to NO₂ exposure. The combined concentration–response curves indicated a linear association. Conclusively, this largest epidemiologic study of NO₂ in Asian developing countries to date suggests that short-term exposure to NO₂ is associated with increased mortality risk.     

Carbon isotopes and sulphur contents as indicators of atmospheric pollution from burning fossil fuels

This paper summarized the study carried out in Krakow, Poland in 1975-76 on the estimated local air pollution as measured by carbon isotopes and total sulphur measurement in plants. Good correlation was found between δ¹⁴C value and the total sulphur (measured by radionuclide excited X-ray fluorescence) in beech leaves collected in the late summer, indicating the common source of both pollutants. Sampling and measurement of σ¹³C in atmospheric CO₂ has shown that σ³C can be used as a pollution indicator only in the winter period when no fluctuations exist ddue to plant respiration. A method of CO₂ sampling using molecular sieve proved to be feasible for instantaneous sampling with no isotope fractionation. The highest pollution by fossil CO₂ was measured in winter (12.8% excess. During spring and summer the average contribution of fossil CO₂ was 4.5 to 5.6%.     

An improved method for Kr analysis by liquid scintillation counting and its application to atmospheric Kr determination

Atmospheric ⁸⁵Kr concentration at Fukuoka, Japan was determined by an improved ⁸⁵Kr analytical method using liquid scintillation counting (LSC). An average value of 1.54 ± 0.05 Bq m⁻³ was observed in 2008, which is about two times that measured in 1981 at Fukuoka, indicating a 29 mBq y⁻¹ rate of increase as an average for these 27 years. The analytical method developed involves collecting Kr from air using activated charcoal at liquid N₂ temperature and purifying it using He at dry ice temperature, followed by Kr separation by gas chromatography. An overall Kr recovery of 76.4 ± 8.1% was achieved when Kr was analyzed in 500-1000 l of air. The Kr isolated by gas chromatography was collected on silica gel in a quartz glass vial cooled to liquid N₂ temperature and the activity of ⁸⁵Kr was measured with a low-background LS counter. The detection limit of ⁸⁵Kr activity by the present analytical method is 0.0015 Bq at a 95% confidence level, including all propagation errors, which is equivalent with ⁸⁵Kr in 1.3 l of the present air under the analytical conditions of 72.1% counting efficiency, 0.1597 cps background count rate, and 76.4% Kr recovery.     

Effect of sample conditioning and chamber loading on rate of formaldehyde release from wood products in a desiccator test

Several variables may influence the observed rate of formaldehyde (CH₂O) offgassing from wood products in a small static test chamber. We studied the effect of sample conditioning at ≈100% relative humidity and chamber loading (sample size) on CH₂O release rate from particle board (PB) and plywood (PW). Samples of PB and PW were placed in glass desiccators with reservoirs of water at a loading of 21 m²/m³ (sample surface area per chamber volume). The rate of CH₂O offgassing from the PB did not change over several weeks under these conditions (0.24 μg/cm²/day), but the overall release rate from the PW decreased after 8 days. In another experiment, the loading of the desiccator had a major effect on the rate of CH₂O offgassing from PB over a loading range of 1 to 42 m²/m³. The same phenomenon was observed with different loadings of PW. The inverse of the observed release rate varied linearly with the chamber loading of PB or PW. At a loading which may be encountered in a house (0.25 m²/m³), the release rate coefficient for PB calculated from the above inverse relation was 22-fold higher than that measured at a more conventional test load of 21 m²/m³. These results indicate that great care should be exercised when using desiccator tests for assessing and comparing the potential strength of materials as sources of CH₂O in the indoor environment.     

Dependence of dose loads on bone surfaces of murine rodents on the level of 90Sr accumulation in the skeleton

The relationship between ⁹⁰Sr accumulation in the skeleton after single injection and the resulting dose load on bone surfaces was studied in laboratory mice. Radiation doses were measured by a thermoluminescent method. A positive correlation was revealed between the surface dose rate on the skull and mandible and ⁹⁰Sr specific radioactivity in these bones. The possibility to calculate ⁹⁰Sr incorporation into the bone tissue from dosimetric data was evaluated as an analytical approach allowing preservation of the bone material for subsequent studies. Conversion coefficients relating surface doses to ⁹⁰Sr specific radioactivity in bones were calculated. However, their values have to be specifically defined for cases of chronic ⁹⁰Sr input and with regard to bone anatomy and species-specific and ecological features of test animals.     

Seasonal variation in outdoor,indoor, and personal air pollution exposures of women using wood stoves in the Tibetan Plateau: Baseline assessment for an energy intervention study

Cooking and heating with coal and biomass is the main source of household air pollution in China and a leading contributor to disease burden. As part of a baseline assessment for a household energy intervention program, we enrolled 205 adult women cooking with biomass fuels in Sichuan, China and measured their 48-h personal exposure to fine particulate matter (PM_2.5) and carbon monoxide (CO) in winter and summer. We also measured the indoor 48-h PM_2.5 concentrations in their homes and conducted outdoor PM_2.5 measurements during 101 (74) days in summer (winter). Indoor concentrations of CO and nitrogen oxides (NO, NO₂) were measured over 48-h in a subset of ~ 80 homes. Women's geometric mean 48-h exposure to PM_2.5 was 80 μg/m³ (95% CI: 74, 87) in summer and twice as high in winter (169 μg/m³ (95% CI: 150, 190), with similar seasonal trends for indoor PM_2.5 concentrations (winter: 252 μg/m³; 95% CI: 215, 295; summer: 101 μg/m³; 95% CI: 91, 112). We found a moderately strong relationship between indoor PM_2.5 and CO (r = 0.60, 95% CI: 0.46, 0.72), and a weak correlation between personal PM_2.5 and CO (r = 0.41, 95% CI: − 0.02, 0.71). NO₂/NO ratios were higher in summer (range: 0.01 to 0.68) than in winter (range: 0 to 0.11), suggesting outdoor formation of NO₂ via reaction of NO with ozone is a more important source of NO₂ than biomass combustion indoors. The predictors of women's personal exposure to PM_2.5 differed by season. In winter, our results show that primary heating with a low-polluting fuel (i.e., electric stove or wood-charcoal) and more frequent kitchen ventilation could reduce personal PM_2.5 exposures. In summer, primary use of a gaseous fuel or electricity for cooking and reducing exposure to outdoor PM_2.5 would likely have the greatest impacts on personal PM_2.5 exposure.     

Direct N2O emission from agricultural soils in Poland between 1960 and 2009

Nitrogen fertilization (N) is commonly known as a main source of direct nitrous oxide (N₂O) emission from agricultural soils. An area of 38 % of the total land surface of Poland was covered by agricultural soils in 2009. In this paper, we aimed at analyzing data regarding the land exploitation for 13 selected subareas of Poland between 1960 and 2009. Seven out of the 13 subareas studied are located in the West (area A), and six subareas are located in southeast of Poland (area B). The total area covered by large farms (>20 ha) differed largely, between area A (10.6 %) and area B (0.9 %) in 2009. Both areas varied in terms of the amount of fertilizers used annually, average crop yield and crop structure. Average direct emissions of N₂O from agricultural soils were 1.66 ± 0.09 kg N₂O–N ha^?1 a^?1 for area A, 1.39 ± 0.07 kg N₂O–N ha^?1 a^?1 for area B and 1.46 ± 0.07 kg N₂O–N ha^?1 a^?1 for the whole country between 1960 and 2009.     

Influence of fertilizing on the Cs soil–plant transfer in a spruce forest of Southern Germany

Fertilization with 2.5 t/ha limestone: (83% CaCO₃, 8% MgO, 6% K₂O, 3% P₂O₅) reduces the ¹³⁷Cs transfer from spruce forest soil into plants like fern (Dryopteris carthusiana) and blackberry (Rubus fruticosus) by a factor of 2–5 during at least 11 years as measured by the aggregated transfer factor T_ag. In 1997 and 2006 these results were confirmed by additional measurements of the ¹³⁷Cs transfer factor TF, related to the root zone (O_h horizon), which were explained by the selective sorption of ¹³⁷Cs in the root zone by measurements of the Radiocaesium Interception Potential (RIP) in fertilized (RIP > 179 meq/kg) and non-fertilized soils (RIP < 74 meq/kg).     

Oxidative potential and chemical composition of PM2.5 in office buildings across Europe – The OFFICAIR study

In the frame of the OFFICAIR project, indoor and outdoor PM_2.5 samples were collected in office buildings across Europe in two sampling campaigns (summer and winter). The ability of the particles to deplete physiologically relevant antioxidants (ascorbic acid (AA), reduced glutathione (GSH)) in a synthetic respiratory tract lining fluid, i.e., oxidative potential (OP), was assessed. Furthermore, the link between particulate OP and the concentration of the PM constituents was investigated.The mean indoor PM_2.5 mass concentration values were substantially lower than the related outdoor values with a mean indoor/outdoor PM_2.5 mass concentration ratio of 0.62 and 0.61 for the summer and winter campaigns respectively. The OP of PM_2.5 varied markedly across Europe with the highest outdoor OP^AA m⁻³ and OP^GSH m⁻³ (% antioxidant depletion/m³ air) values obtained for Hungary, while PM_2.5 collected in Finland exhibited the lowest values. Seasonal variation could be observed for both indoor and outdoor OP^AA m⁻³ and OP^GSH m⁻³ with higher mean values during winter. The indoor/outdoor OP^AA m⁻³ and OP^GSH m⁻³ ratios were less than one with 4 and 17 exceptions out of the 40 cases respectively. These results indicate that indoor air is generally less oxidatively challenging than outdoors. Correlation analysis revealed that trace elements play an important role in determining OP, in particular, the Cu content. Indoor air chemistry might affect OP since weaker correlations were obtained for indoor PM_2.5. Our findings also suggest that office workers may be exposed to health relevant PM constituents to a different extent within the same building.