Photolysis of polycyclic aromatic hydrocarbons adsorbed on spruce [Picea abies (L) Karst] needles under sunlight irradiation

Photolysis of polycyclic aromatic hydrocarbons (PAHs) sorbed on surfaces of spruce [Picea abies (L.) Karst.] needles under sunlight irradiation was investigated. PAHs were produced by combustion of polyvinyl chloride (PVC), wood, high-density polyethylene (HDPE), and styrene in a stove. The factors of sunlight irradiation on the surfaces of spruce needles were taken into consideration when investigating the kinetic parameters. The photolysis of the 18 PAHs under study follows first-order kinetics. The photolysis half-lives range from 15 h for dibenzo(a,h)anthracene to 75 h for phenanthrene. Photolysis of some PAHs on surfaces of spruce needles may play an important role on the fate of PAHs in the environment.     

Investigations on the binding mechanism of the herbicide simazine to dissolved organic matter in leachates of compost

14C-labelled simazine was composted together with biowaste on a pilot (m3) scale. The herbicide was quickly bound to the compost matrix. By aqueous extraction of 29 and 200 days old compost (equivalent to thermophilic and mesophilic phase of composting) only 4.2% and 3.1% respectively of the radioactivity in the compost samples could be extracted with water. Analysis of the extracts using high-performance size exclusion chromatography (HPSEC) revealed that the dissolved organic matter (DOM) had molecular weights ranging between 2 and 28 kDa. The amount of DOM-associated radioactivity increased from 53% (day 29) to 65% (day 200) of total extractable radioactivity. The type of binding of the 14C-labelled residues and the DOM was elucidated by silylation of humic matter and subsequent HPSEC. The data demonstrated that besides polar metabolites also intact simazine was bound to the DOM. A distinct shift from rather weak interactions to strong covalent linkages of simazine and its metabolites with increasing age of the compost was observed. The results showed that only low amounts of free simazine and its degradates can be extracted with water. We concluded that the shift towards stable covalent linkages is equivalent to a detoxification of the contaminant in aged compost. Consequently, the use of the analysed compost in its mature stage should not pose an environmental risk to the groundwater or the subsoil.     

Regional analysis of global change impacts: Concepts, tools and first results

The paper introduces an approach for the analysis of global change impacts on river basins or regions. This approach is quite general and can be transferred to any region or river basin of interest on earth. The first application of the approach was in the Elbe river basin, with primary focus on the hydrologic model part and on the integration of crop growth and nitrogen dynamics. Finally, concepts for the integration of socio-economic aspects in the analysis are introduced.     

The European Water Framework Directive beyond 2010: let actions speak louder than words

The first generation of WFD River Basin Management Plans is now available. This is a formidable achievement and a great step towards addressing Europe's deteriorated river systems. However, plans are only words: only the actual implementation of the selected measures will result in achievement of good ecological and chemical status. The WFD Lille 2010 Conference pointed out that a lot of new, but so far unused scientific knowledge is available to improve the effectiveness of selected measures or to inspire the introduction of complementary measures. Furthermore, the complexity in terms of the functioning of the water system, its interaction with the socio-economic system and the uncertain consequences of climate change, urges a 'learning-by-doing' approach. This approach should be applied in well-designed, -coordinated and -monitored learning catchments.     

Thorium and uranium contents in human urine: influence of age and residential area

Inductively coupled plasma mass spectrometry (ICP-MS) has been used for the determination of (232)Th and (238)U in urine of unexposed Jordanian subjects living in six cities. The range of (232)Th excretion in all subjects was found to be 1.4-640 microBq d(-1) with an average of 34.8 microBq d(-1) (geometric mean 15.8 microBq d(-1)). Results showed no statistically significant correlation with age and residential area. The average value obtained is in agreement with levels considered normal in some recent publications. The average value of (238)U in all samples was found to be 3955 microBq d(-1) (geometric mean 1107 microBq d(-1)), which is higher than reported figures from Germany and India, but in agreement with those figures given in ICRP publication, number 23. The mean values of the different groups were found to be proportional to age up to 60 years. A noticeable drop is observed for subjects greater than 60 years old.     

Regional dependence of urinary uranium baseline levels in non-exposed subjects with particular reference to volunteers from Northern Italy

Knowledge of the level of natural uranium (U) in the human body is fundamental in order to estimate the potentially hazardous incorporation in accidentally exposed subjects. A constant monitoring of exposed workers needs reliable reference baseline values, which can be determined by measuring the U concentration in urine. ICPMS has proven to be a fast, reliable and highly sensitive technique for this purpose. Non-uniformity in the distribution of U levels in various regions and differences in dietary habits account for the significant regional variations of U concentration in urine in non-exposed subjects. In this paper, the determination of daily uranium urinary excretion levels in a group of 12 non-exposed subjects from Northern Italy is presented and compared to data present in the published literature and to values obtained in a larger group of German volunteers. The urinary U output values observed in the Italian subset are generally higher than the corresponding levels measured in other groups. This could be the result of a higher intake of U from liquids, as assessed by the determination of U concentration in drinking waters.     

Critical evaluation of PAH source apportionment tools using data from the Swiss soil monitoring network

In this study a large dataset on the polycyclic aromatic hydrocarbon (PAH) content of Swiss soils was analysed to evaluate two source apportionment tools, i.e., characteristic PAH ratios/molecular markers and a linear mixing model. Population density and total organic carbon (TOC) content were identified by a multiple regression model as independently and positively influencing the PAH concentrations in Swiss background soil. Specifically, TOC was more strongly positively correlated with the sum of light PAH (naphthalene to phenanthrene) than with the sum of heavy PAH (anthracene to benzo[ghj]perylene), whereas population density was more strongly positively correlated with the sum of heavy PAH than with light PAH. In addition, the sum of the heavy PAH as well as the total sum correlated negatively with sample site altitude. It is therefore hypothesised that heavy PAH are less mobile, whereas light PAH were closer to equilibrium with TOC in the soil. Similar results were found for polychlorinated biphenyls (PCB). The characteristic ratios and molecular markers pointed to pyrogenic origin of PAH in Swiss background soil but did not allow for further differentiation of individual fuel contributions, even though attempts to take environmental fractionation processes into account were made. The comparison of three soil profiles identified with a linear mixing model from the pattern of 16 PAH with >300 PAH emission profiles from the literature suggested urban dust, wood combustion and binders from asphalt as PAH sources. However, also here, environmental fractionation processes probably obscured source characteristic PAH ratios and fingerprints, which thus need to be interpreted with caution.     

Stable isotopes (δ18O and δ13C) in Spirula spirula shells from three major oceans indicate developmental changes paralleling depth distributions

Stable isotopes (δ¹⁸O and δ¹³C) were measured in successive chambers of the aragonitic shells of the small deep-sea squid Spirula spirula (Linnaeus 1758) (class Cephalopoda, subclass Coleoidea, order Sepioidea, family Spirulidae) to determine whether their depth distributions change with age. The spiral shells, ranging in diameter from 18 to 23 mm (30–38 chambers), were collected between 2000 and 2006 from beaches in six widely separated locations in three oceans, the Atlantic (Tobago and Canary Islands), Indian (Madagascar, Maldives, and Perth, Australia), and Pacific Oceans (Ulladulla, Australia). The patterns for both isotopes were highly correlated in specimens from all six sites. The δ¹⁸O data suggest that after hatching at depths >1,000 m at temperatures of 4–6°C, the squid migrate into shallower, warmer waters at 12–14°C at depths of 400–600 m. Subsequently, the increasing δ¹⁸O values suggest a migration back into somewhat cooler, deeper habitats. The δ¹³C values also revealed three ontogenetic stages in all six specimens, including a major shift from positive to negative values, which probably corresponds to sexual maturation, the initiation of reproduction, and concomitant changes in diet. In three of the six specimens (from Tobago, Canary Islands, and Maldives) a fourth embryonic stage (not detected in the oxygen data) was accompanied by markedly less positive δ¹³C values in the first few chambers. These data, combined with the scanty life history information from previous studies of S. spirula, can be used to compare the habitat requirements of related extant and fossil cephalopod genera. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.