Untersuchungskonzept zur Charakterisierung toxischer Stoffe in belastetem Wasser

Zusammenfassung  Zur ?kotoxikologischen Beurteilung von belastetem Wasser werden h?ufig einfache Biotests eingesetzt. Nicht selten werden dabei toxische Effekte festgestellt. Es stellt sich dann die Frage nach den verantwortlichen Wasserinhalts-stoffen. Durch Festphasenextraktion (SPE) werden diese angereichert, gewonnen und dünnschichtchromatographisch unter Verwendung der automatisierten Mehrfachentwicklung aufgetrennt. Von der DC-Platte wird ein Streifen abgetrennt und darauf direkt die biologische Detektion mit Mikroorganismen (Bacillus subtilis, Leuchtbakterien) durchgeführt. Dadurch k?nnen toxische Banden erkannt werden, Auf dem DC-Plattenrest wird von der toxischen Bande mit einem DC-scanner ein UV-Spektrum aufgenommen, die entsprechende Bande herausgekratzt, der toxische Stoff eluiert und infrarotspektroskopisch untersucht. Durch Spektrenvergleich gelingt es meistens, den Stoff zu charakterisieren. In der vorliegenden Arbeit wird am Beispiel eines Zitzengummieluates das Analysenkonzept vorgestelit. Es zeigte sich, dass dieser Gummiartikel einen Vulkanisationsbeschleuniger (2-Mercaptobenzothiazol) freisetzt. Online-Publikation am: 21.12.1999     

Absch?tzung der Quecksilberexposition

Zusammenfassung  Ein quecksilberkontaminierter Altstandort dient als Beispiel für eine umweltmedizinische Beurteilung der Belastung der im Umfeld wohnenden Personen durch Quecksilberimmissionen. Dabei wird die innere Exposition für sieben verschiedene Altersgruppen bezüglich der KontaktmedienBoden, Luft undNahrungsmittel anhand von konventionell festgelegten Szenarien abgesch?tzt und ein Vergleich mit den epidemiologischen Ergebnissen eines Humanmonitorings angestrebt. Die standortspezifisch und pfadspezifisch durchgeführte Expositionsabsch?tzung stützt sich auf cine Vielzahl von unterschiedlichen Probenehmern sowie auf über mehrere Jahre durchgeführte Konzentrationsmessungen in den aufnahmerelevanten Kompartimenten. Sowohl die Berechnungen als auch die epidemiologischen Untersuchungen zeigen eine leichte Erh?hung der Quecksilberexposition, gemessen an strengen Richtwerten.      

Temporal variations of atmospheric aerosol in four European urban areas

Purpose

The concentrations of PM₁₀ mass, PM_2.5 mass and particle number were continuously measured for 18 months in urban background locations across Europe to determine the spatial and temporal variability of particulate matter.

Methods

Daily PM₁₀ and PM_2.5 samples were continuously collected from October 2002 to April 2004 in background areas in Helsinki, Athens, Amsterdam and Birmingham. Particle mass was determined using analytical microbalances with precision of 1 ??g. Pre- and post-reflectance measurements were taken using smoke-stain reflectometers. One-minute measurements of particle number were obtained using condensation particle counters.

Results

The 18-month mean PM₁₀ and PM_2.5 mass concentrations ranged from 15.4 ??g/m³ in Helsinki to 56.7 ??g/m³ in Athens and from 9.0 ??g/m³ in Helsinki to 25.0 ??g/m³ in Athens, respectively. Particle number concentrations ranged from 10,091 part/cm³ in Helsinki to 24,180 part/cm³ in Athens with highest levels being measured in winter. Fine particles accounted for more than 60% of PM₁₀ with the exception of Athens where PM_2.5 comprised 43% of PM₁₀. Higher PM mass and number concentrations were measured in winter as compared to summer in all urban areas at a significance level p?Conclusions Significant quantitative and qualitative differences for particle mass across the four urban areas in Europe were observed. These were due to strong local and regional characteristics of particulate pollution sources which contribute to the heterogeneity of health responses. In addition, these findings also bear on the ability of different countries to comply with existing directives and the effectiveness of mitigation policies.     

Monitoring, modelling and environmental exposure assessment of industrial chemicals in the aquatic environment

Monitoring and laboratory data play integral roles alongside fate and exposure models in comprehensive risk assessments. The principle in the European Union Technical Guidance Documents for risk assessment is that measured data may take precedence over model results but only after they are judged to be of adequate reliability and to be representative of the particular environmental compartments to which they are applied. In practice, laboratory and field data are used to provide parameters for the models, while monitoring data are used to validate the models' predictions. Thus, comprehensive risk assessments require the integration of laboratory and monitoring data with the model predictions. However, this interplay is often overlooked. Discrepancies between the results of models and monitoring should be investigated in terms of the representativeness of both. Certainly, in the context of the EU risk assessment of existing chemicals, the specific requirements for monitoring data have not been adequately addressed. The resources required for environmental monitoring, both in terms of manpower and equipment, can be very significant. The design of monitoring programmes to optimise the use of resources and the use of models as a cost-effective alternative are increasing in importance. Generic considerations and criteria for the design of new monitoring programmes to generate representative quality data for the aquatic compartment are outlined and the criteria for the use of existing data are discussed. In particular, there is a need to improve the accessibility to data sets, to standardise the data sets, to promote communication and harmonisation of programmes and to incorporate the flexibility to change monitoring protocols to amend the chemicals under investigation in line with changing needs and priorities.     

Resistant sorption of in situ chlorobenzenes and a polychlorinated biphenyl in river Rhine suspended matter

The desorption kinetics of in situ chlorobenzenes (dichlorobenzenes, pentachlorobenzene and hexachlorobenzene) and 2,4,4^′-trichlorobiphenyl (PCB-28) were measured with a gas-purge technique for river Rhine suspended matter sampled in Lobith, The Netherlands. This suspended matter is the main source of sediment accumulation in lake Ketelmeer. In lake Ketelmeer sediment earlier observations showed that slow and very slow fractions dominate the desorption profile.

For the river Rhine suspended matter, only for PCB-28 a fast desorbing fraction of around 1.6% could be detected. The observed rate constants were on the average 0.2 h⁻¹ for fast desorption, 0.004 h⁻¹ for slow desorption, and 0.00022 h⁻¹ for very slow desorption. These values are in agreement with previous findings for the sediment from lake Ketelmeer and with available literature data on fast, slow, and very slow desorption kinetics.

The results from this study show the similarity of desorption profiles between river Rhine suspended matter, and the top layer sediment from lake Ketelmeer. This indicates that slow and very slow fractions are already present in material forming the top layer of lake Ketelmeer, and were not formed after deposition of this material in the lake. The absence of detectable fast fractions for most compounds could be caused by the absence of recent pollution of the suspended matter. But, the observations may also be explained by a rapid disappearance of compounds from the fast fraction due to a combination of a high affinity of very slow sites for these compounds, and their relatively high volatility.     

中国西部本底大气中CO的连续测量

在中国西北部的瓦里关全球基准站(36°17'N,100°54'E,3810m asl)建立了气相色谱-汞置换法大气CO连续测量系统.组装调试和运行标定表明,色谱方法的基线稳定,分离度高,检测方法可靠,系统具有高自动化的操作性能和严格的质量控制,其设计完全符合世界气象组织(WMO)全球大气本底测量的要求.根据采样现场大气CO浓度的变化,采用经国际比对的CO标准气系列,用峰高外标法设定可调整的标准工作曲线计算环境CO浓度,系统对CO的检测限低至1×10^-9(V/V),检测精度小于0.1%,准确度在±0.05%以内,可提供我国本底地区近地层大气CO连续而精确的现场测量结果.