Resilience of epilithic algal assemblages in atmospherically and experimentally acidified boreal lakes

Algal assemblages can be highly responsive to environmental changes in recovering acidified lakes. We compared epilithic algal assemblages in boreal lakes during chemical recovery from atmospheric (Killarney Park, Ontario) and experimental (Lake 302S, Experimental Lakes Area, Ontario) acidification to assess the impact of spatial and temporal scale of severe acidification on taxonomic resilience (i.e. recovery rate). Resilience was measured as the distance traveled by lakes in ordination space during pH recovery based on canonical correspondence analysis. Resilience was relatively negligible in the Killarney lakes, suggesting that eight years of experimental acidification in Lake 302S had less impact on biological recovery than did decades of regional acidification. Increases in dissolved organic carbon, dissolved inorganic carbon, and calcium best explained temporal variance of epilithic species abundances in the recovering acidified lakes. In Lake 302S, contrasting trajectories of taxonomic resilience and resistance, i.e. displacement from reference conditions following a perturbation, indicated that ecological factors affecting epilithon differed at corresponding pH levels during recovery and acidification. Our findings reveal that modeling of ecosystem recovery from severe acidification must account for the spatial and temporal scale of the perturbation, and biological delay responses that result in differences between recovery and acidification trajectories.     

Anthropogenic NOx emissions alter the intrinsic water-use efficiency (WUEi) for Quercus cerris stands under Mediterranean climate conditions

We investigated the effect of N deposition (Ndep) on intrinsic water-use efficiency (WUE_i), the ratio of photosynthesis (A) to stomatal conductance (g_s), for two Quercus cerris stands at different distances to an oil refinery in Southern Italy. We used δ¹³C in tree rings for assessing changes in WUE_i; while the influence of climate and NO_x emission was explored through δ¹⁸O and δ¹⁵N, respectively. Differences in WUE_i between the two sites were significant, with trees exposed to different degrees of NO_x emissions showing an abrupt increase with the onset of pollution. Assuming similar g_s at the two sites, as inferred through δ¹⁸O, the higher N availability at the polluted site caused the shift of the A/g_s ratio in favour of A. Overall, our result suggests that an increase of Ndep may enhance tree WUE under a scenario of reduction of precipitation predicted for Mediterranean area.     

Quecksilbergasfeinreinigung mittels metall- und salzpartikelbelegter Tr?germaterialien (G/S-Reaktor) ?kotoxizit?t von Quecksilber und seiner Verbindungen

Zusammenfassung  Bei einer genauen Kenntnis der vorliegenden Quecksilberverbindungen und ihrem Verhalten im Rauchgaspfad thermischer Anlagen k?nnen durch entsprechende technische Ma?nahmen die Abscheideeffizienzen in trockenen, quasitrockenen und nassen Rauchgasreinigungsanlagen erheblich gesteigert werden, so da? der derzeit gesetzlich vorgeschriebene Emissionsgrenzwert von 50 μg/m³ [i.N.tr.] eingehalten und unterschritten wird. Die in den letzten Jahren unternommenen Aktivit?ten und Fortschritte bei der Reduzierung des Quecksilberaussto?es von thermischen Anlagen werden zusammenfassend dargestellt. Am Beispiel von tr?gerimmobilisierten metall- und/oder metallsalzpartikelbelegten Tr?germaterialien (G/S-Reaktoren) wird die selektive Entfernung des Quecksilbers bzw. dessen Verbindungen experimentell und theoretisch im Rauchgaspfad verdeutlicht. Aus der selektiven Abtrennung von Quecksilber und seinen Verbindungen in der Gasphase resultieren auch entsprechende ?kologische und ?konomische Vorteile, die den allgemein erkennbaren Trend der artspezifischen Abtrennung von Schadstoffen mit einer m?glichen Rückführung des Wertstoffes Quecksilber in den Wirtschaftskreislauf unterstützen.      

Quantitative determination of de-conjugated chrysene metabolites in fish bile by HPLC-fluorescence and GC--MS

Two analytical methods have been evaluated for quantitative determination of de-conjugated chrysene metabolites in fish bile. High performance liquid chromatography-fluorescence (HPLC-F) and gas chromatography-mass spectrometry (GC--MS) were compared regarding instrumental and overall limits of detection (LOD) as well as recoveries for the following nine chrysene compounds: 1-, 2,- 3-, 4- and 6-hydroxychrysene (1-, 2-, 3-, 4- and 6-OH-chr), 1,2-dihydroxy-1,2-dihydrochrysene (1,2-DHD-chr), 3,4-dihydroxy-3,4-dihydrochrysene (3,4-DHD-chr), 5,6-dihydroxy-5,6-dihydrochrysene (5,6-DHD-chr) and chrysene. Instrumental LODs were comparable for the two methods whereas the overall LOD was better for HPLC-F. Recoveries varied per chrysene compound for both HPLC-F (62-107%) and GC-MS (48-124%). In vivo formed chrysene metabolites were studied in the bile of Atlantic cod (Gadus morhua) exposed to chrysene (1 mg/kg) via intra-peritoneal (i.p.) and inter-muscular (i.m.) injection. Total amounts of chrysene metabolites were three times higher in i.p. compared to i.m. exposed cod bile, but the relative distribution of determined metabolites was very similar. 1,2-DHD-chr was the most prominent metabolite in de-conjugated bile and constituted more than 88% of the total chrysene metabolites. Additional chrysene metabolites formed were 3,4-DHD-chr and 1-, 2-, 3- and 4-OH-chr. K-region chrysene metabolites (oxidation at carbons 5 and 6) were not detected and seem to be a less favoured biotransformation route. The two methods were applied and evaluated for analysis of chrysene metabolites in two bile reference materials (BCR 720 and 721) and a limited number of field exposed cods.     

Identification of soil contamination hotspots with veterinary antibiotics using heavy metal concentrations and leaching data—a field study in China

In regions with high livestock densities, the usage of antibiotics and metals for veterinary purposes or as growth promoters poses a risk in manured soils. We investigated to which degree the concentrations and depth distributions of Cu, Zn, Cr and As could be used as a tracer to discover contaminations with sulfonamides, tetracyclines and fluoroquinolones. Besides, we estimated the potential vertical translocation of antibiotics and compared the results to measured data. In the peri-urban region of Beijing, China, soil was sampled from agricultural fields and a dry riverbed contaminated by organic waste disposal. The antibiotic concentrations reached 110 μg kg^?1 sulfamethazine, 111 μg kg^?1 chlortetracycline and 62 μg kg^?1 enrofloxacin in the topsoil of agricultural fields. Intriguingly, total concentrations of Cu, Zn, Cr and As were smaller than 65, 130, 36 and 10 mg kg^?1 in surface soil, respectively, therewith fulfilling Chinese quality standards. Correlations between sulfamethazine concentrations and Cu or Zn suggest that in regions with high manure applications, one might use the frequently existing monitoring data for metals to identify potential pollution hotspots for antibiotics in topsoils. In the subsoils, we found sulfamethazine down to ≥2 m depth on agricultural sites and down to ≥4 m depth in the riverbed. As no translocation of metals was observed, subsoil antibiotic contamination could not be predicted from metal data. Nevertheless, sulfonamide stocks in the subsoil could be estimated with an accuracy of 35–200 % from fertilisation data and potential leaching rates. While this may not be sufficient for precise prediction of antibiotic exposure, it may very well be useful for the pre-identification of risk hotspots for subsequent in-depth assessment studies.     

Evaluating Controlling Factors to Ali/(Ca + Mg) Molar Ratio in Acidic Soil Water, Southern and Southwestern China: Multivariate Approach

Al_i/(Ca + Mg) molar ratio in soil water has been used as an indicator to the effects of acid deposition on terrestrial ecosystems. However, the main factors controlling this ratio have not been well documented in southern and southwestern China. In this study, we presented the variation in inorganic aluminum (Al_i) and Al_i/(Ca + Mg) molar ratio in different sites and soil horizons based on two to three years monitoring data, and evaluated the main factors controlling Al_i/(Ca + Mg) molar ratio using principle component analysis (PCA) and partial least square (PLS) regression. Monitoring data showed although Al_i/(Ca + Mg) molar ratios in most soil water were lower than assumed critical 1.0, higher molar ratios were found in some soil water at TSP and LXH site. Besides acid loading, both soil properties and soil water chemistry affected the value of Al_i/(Ca + Mg) molar ratio in soil water. Partial least square (PLS) indicated that they had different relative importance in different soil horizons. In A-horizon, soil aluminum saturation (AlS) had higher influence on Al_i/(Ca + Mg) molar ratio than soil water chemistry did; higher soil aluminum saturation (AlS) led to higher Al_i/(Ca + Mg) molar ratio in soil water. In the deeper horizons (i.e., B₁-, B₂- and BC-horizon), inorganic aluminum (Al_i) in soil water had more and more important role in regulating Al_i/(Ca + Mg) molar ratio. On regional scale, soil aluminum saturation (AlS) as well as cation exchange capacity (CEC) was the dominant factor controlling Al_i/(Ca + Mg) molar ratio. This should be paid enough attention on when making regional acid rain control policy in China.     

EcoEffect for outdoor environments; the process of tool development

Numerous evaluation tools for the built environment have been developed in recent decades only some however integrate the outdoor environment. In EcoEffect, a Swedish assessment system, the outdoor environment is one of five areas covered. The purpose of this article is to describe and discuss various issues that evolved during the testing and developing phase of the EcoEffect Outdoor tool. The tool is designed to cover all important health risks to people in an outdoor environment, to show the relationship between circumstances in the outdoor environment and the levels specified in Swedish legislation and to enable a speedy and accurate assessment of the outdoor environment on a property. The work has been carried out in cooperation with experts, residents and representatives of the construction and property sectors. The tool has been tested on existing properties, discussed in focus groups, and has been subject to theoretical development. The results have provided a basis for changing both the EcoEffect Outdoors tool and the framework of the EcoEffect system. Important conclusions here include the notion that a clear account should be given of the fundamental values of the tool, that environmental impact should be reported in the same way throughout the whole assessment process and that the tool has to adhere to both scientific and practical validity to be useful for the building sector.     

Prüfung und Bewertung der Auswirkungen von Pflanzenschutzmitteln auf terrestrische Organismen nach der EG-Richtlinie 91/414/EWG

EU Directive 91/414/EEC describes the authorization procedure for plant protection products. According to annex VI of this directive, the EU member states have to ensure that a plant protection product does not have unacceptable effects on the environment. The data requirements and the function of laboratory and field tests in the assessment procedure are discussed for the terrestrial compartment.