RESUMEN
Residential wood combustion contributing to airborne particulate matter (PM10) was studied for 1 year at two sites in the village of Melpitz. Significant excess pollution was observed at the Melpitz center compared to that at the TROPOS research station Melpitz reference site, situated only 700 m away. Local concentration increments at the village site for the combustion PM constituents organic carbon, elemental carbon, levoglucosan, and benzo[a]pyrene were determined under appropriate wind directions, and their winter mean values were 0.7 µg m-3, 0.3 µg m-3, 0.1 µg m-3, and 0.4 ng m-3, representing relative increases over the regional background concentration of 24, 70, 61, and 107%, respectively. Yearly, weekly, and diurnal profiles of village increments suggest residential heating as the dominant source of this excess pollution, mainly originating from wood combustion. Receptor modeling using positive matrix factorization quantified 4.5 µg m-3 wood combustion PM at the village site, representing an increment of 1.9 µg m-3 and an increase of â¼75% over the 2.6 µg m-3 regional background wood combustion PM. This increment varied with season, temperature, and boundary layer height and reached daily mean values of 4-6 µg m-3 during unfavorable meteorological conditions. Potential health effects were estimated and resulted in an all-cause mortality from short-term exposure to wood combustion PM of 2.1 cases per 100,000 inhabitants and year for areas with similar wood smoke levels as observed in Melpitz. The excess cancer risk from the concentrations of polycyclic aromatic hydrocarbons was 6.4 per 100,000. For both health metrics, the very local contributions from the village itself were about 40-50%, indicating a strong potential for mitigation through local-scale policies. A compilation of literature data demonstrates wood combustion to represent a major source of PM pollution in Germany, with average winter-time contributions of 10-20%. The present study quantifies the negative impacts of heating with wood in rural residential areas, where the continuous monitoring of air quality is typically lacking. Further regulation of this PM source is warranted in order to protect human health.
RESUMEN
Phytoscreening of phytoremediation-based plantings is discussed as a promising monitoring tool in literature. We developed and applied an analytical procedure for the in vivo sampling of methyl tert-butyl ether (MTBE) in the common reed (Phragmites australis) from a phytoremediation site highly polluted with MTBE. The approach uses solid-phase microextraction (SPME) with the SPME fibre directly introduced into the aerenchyma of the plant stem. For optimising the analytical procedure and estimating the capability of the proposed method, laboratory tests on the microcosm scale and field studies over one vegetation period were carried out. Furthermore, the results of in vivo SPME sampling were compared with those obtained with the traditional approach for analysing plants using dynamic headspace analysis. The MTBE signals detected within the plants were also correlated with the concentration in the water phase. The discussion of results showed the feasibility of the proposed method for a qualitative phytoscreening of volatile organic compounds present in wetland plants.
Asunto(s)
Éteres Metílicos/análisis , Poaceae/química , Microextracción en Fase Sólida/métodos , Compuestos Orgánicos Volátiles/análisis , Contaminantes Químicos del Agua/análisis , Biodegradación Ambiental , Monitoreo del Ambiente/métodos , HumedalesRESUMEN
In order to investigate the fate of volatile pollutants such as methyl tert-butyl ether (MTBE) and benzene during the treatment of contaminated water using constructed wetlands, appropriate analytical methods for the analysis of wetland marsh plants, in our case common reed (Phragmites australis), are required. Different sampling procedures and different headspace (HS) based sample preparation techniques were examined to select and establish the most suited procedure for determining the target analytes in plant material. Static HS, dynamic HS and HS solid phase microextraction (SPME) in combination with GC-MS were optimized and evaluated regarding the extraction yields and their capability for quantitative analysis. Only dynamic HS analysis at 80 degrees C for 45min with trapping the analytes on Tenax TA/Chromosorb-106 desorption tubes and the subsequent thermodesorption GC-MS permits the quantitative analysis of MTBE and benzene in reed in a concentration range from 4ng up to 4mug per sample weight (approximately 1g). Static HS and HS SPME analyses were found to be less reliable due to the lack of suitable reference materials. Therefore, these methods do not permit the accurate quantification of pollutant content. Additionally, the HS SPME method is characterized by a restricted linear range of calibration curves. The optimized dynamic HS method was successfully applied for the quantitative analysis of MTBE and benzene within the plants. Their distribution within the plant depending on its height shows a different behavior due to differences in degradability of both substances. While a strong decrease of the concentration of benzene with increasing height of plant was found, the decrease of the concentration of MTBE was not as obvious as observed for benzene. Furthermore, the assessment of plant uptake during phytoremediation was demonstrated by analyzing complete plants for the constructed wetlands investigated.