B. Stieger, G. Spindler, B. Fahlbusch, K. Müller, A. Grüner, L. Poulain, L. Thöni, E. Seitler, M. Wallasch, H. Herrmann
{"title":"在德国Melpitz研究站用MARGA在线系统测量PM10离子和微量气体——一项为期五年的研究","authors":"B. Stieger, G. Spindler, B. Fahlbusch, K. Müller, A. Grüner, L. Poulain, L. Thöni, E. Seitler, M. Wallasch, H. Herrmann","doi":"10.1007/s10874-017-9361-0","DOIUrl":null,"url":null,"abstract":"<p>An hourly quantification of inorganic water-soluble PM<sub>10</sub> ions and corresponding trace gases was performed using the Monitor for AeRosols and Gases in ambient Air (MARGA) at the TROPOS research site in Melpitz, Germany. The data availability amounts to over 80% for the five-year measurement period from 2010 to 2014. Comparisons were performed for the evaluation of the MARGA, resulting in coefficients of determinations (slopes) of 0.91 (0.90) for the measurements against the SO<sub>2</sub> gas monitor, 0.84 (0.88), 0.79 (1.39), 0.85 (1.20) for the ACSM NO<sub>3</sub>\n <sup>?</sup>, SO<sub>4</sub>\n <sup>2?</sup> and NH<sub>4</sub>\n <sup>+</sup> measurements, respectively, and 0.85 (0.65), 0.88 (0.68), 0.91 (0.83), 0.86 (0.82) for the filter measurements of Cl<sup>?</sup>, NO<sub>3</sub>\n <sup>?</sup>, SO<sub>4</sub>\n <sup>2?</sup> and NH<sub>4</sub>\n <sup>+</sup>, respectively. A HONO comparison with a batch denuder shows large scatter (R<sup>2</sup> = 0.41). The MARGA HNO<sub>3</sub> is underestimated compared to a batch and coated denuder with shorter inlets (slopes of 0.16 and 0.08, respectively). Less NH<sub>3</sub> was observed in coated denuders for high ambient concentrations. Long-time measurements show clear daily and seasonal variabilities. Potential Source Contribution Function (PSCF) analysis indicates the emission area of particulate ions Cl<sup>?</sup>, NO<sub>3</sub>\n <sup>?</sup>, SO<sub>4</sub>\n <sup>2?</sup>, NH<sub>4</sub>\n <sup>+</sup>, K<sup>+</sup> and gaseous SO<sub>2</sub> to lie in eastern European countries, predominantly in wintertime. Coarse mode sea salt particles are transported from the North Sea to Melpitz. The particles at Melpitz are nearly neutralised with a mean molar ratio of 0.90 for the five-year study. A slight increase of the neutralization ratio over the last three years indicates a stronger decrease of the anthropogenically emitted NO<sub>3</sub>\n <sup>?</sup> and SO<sub>4</sub>\n <sup>2?</sup> compared to NH<sub>4</sub>\n <sup>+</sup>.</p>","PeriodicalId":611,"journal":{"name":"Journal of Atmospheric Chemistry","volume":"75 1","pages":"33 - 70"},"PeriodicalIF":3.0000,"publicationDate":"2017-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s10874-017-9361-0","citationCount":"38","resultStr":"{\"title\":\"Measurements of PM10 ions and trace gases with the online system MARGA at the research station Melpitz in Germany – A five-year study\",\"authors\":\"B. Stieger, G. Spindler, B. Fahlbusch, K. Müller, A. Grüner, L. Poulain, L. Thöni, E. Seitler, M. Wallasch, H. Herrmann\",\"doi\":\"10.1007/s10874-017-9361-0\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>An hourly quantification of inorganic water-soluble PM<sub>10</sub> ions and corresponding trace gases was performed using the Monitor for AeRosols and Gases in ambient Air (MARGA) at the TROPOS research site in Melpitz, Germany. The data availability amounts to over 80% for the five-year measurement period from 2010 to 2014. Comparisons were performed for the evaluation of the MARGA, resulting in coefficients of determinations (slopes) of 0.91 (0.90) for the measurements against the SO<sub>2</sub> gas monitor, 0.84 (0.88), 0.79 (1.39), 0.85 (1.20) for the ACSM NO<sub>3</sub>\\n <sup>?</sup>, SO<sub>4</sub>\\n <sup>2?</sup> and NH<sub>4</sub>\\n <sup>+</sup> measurements, respectively, and 0.85 (0.65), 0.88 (0.68), 0.91 (0.83), 0.86 (0.82) for the filter measurements of Cl<sup>?</sup>, NO<sub>3</sub>\\n <sup>?</sup>, SO<sub>4</sub>\\n <sup>2?</sup> and NH<sub>4</sub>\\n <sup>+</sup>, respectively. A HONO comparison with a batch denuder shows large scatter (R<sup>2</sup> = 0.41). The MARGA HNO<sub>3</sub> is underestimated compared to a batch and coated denuder with shorter inlets (slopes of 0.16 and 0.08, respectively). Less NH<sub>3</sub> was observed in coated denuders for high ambient concentrations. Long-time measurements show clear daily and seasonal variabilities. Potential Source Contribution Function (PSCF) analysis indicates the emission area of particulate ions Cl<sup>?</sup>, NO<sub>3</sub>\\n <sup>?</sup>, SO<sub>4</sub>\\n <sup>2?</sup>, NH<sub>4</sub>\\n <sup>+</sup>, K<sup>+</sup> and gaseous SO<sub>2</sub> to lie in eastern European countries, predominantly in wintertime. Coarse mode sea salt particles are transported from the North Sea to Melpitz. The particles at Melpitz are nearly neutralised with a mean molar ratio of 0.90 for the five-year study. A slight increase of the neutralization ratio over the last three years indicates a stronger decrease of the anthropogenically emitted NO<sub>3</sub>\\n <sup>?</sup> and SO<sub>4</sub>\\n <sup>2?</sup> compared to NH<sub>4</sub>\\n <sup>+</sup>.</p>\",\"PeriodicalId\":611,\"journal\":{\"name\":\"Journal of Atmospheric Chemistry\",\"volume\":\"75 1\",\"pages\":\"33 - 70\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2017-04-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1007/s10874-017-9361-0\",\"citationCount\":\"38\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Atmospheric Chemistry\",\"FirstCategoryId\":\"89\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s10874-017-9361-0\",\"RegionNum\":4,\"RegionCategory\":\"地球科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENVIRONMENTAL SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Atmospheric Chemistry","FirstCategoryId":"89","ListUrlMain":"https://link.springer.com/article/10.1007/s10874-017-9361-0","RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
Measurements of PM10 ions and trace gases with the online system MARGA at the research station Melpitz in Germany – A five-year study
An hourly quantification of inorganic water-soluble PM10 ions and corresponding trace gases was performed using the Monitor for AeRosols and Gases in ambient Air (MARGA) at the TROPOS research site in Melpitz, Germany. The data availability amounts to over 80% for the five-year measurement period from 2010 to 2014. Comparisons were performed for the evaluation of the MARGA, resulting in coefficients of determinations (slopes) of 0.91 (0.90) for the measurements against the SO2 gas monitor, 0.84 (0.88), 0.79 (1.39), 0.85 (1.20) for the ACSM NO3?, SO42? and NH4+ measurements, respectively, and 0.85 (0.65), 0.88 (0.68), 0.91 (0.83), 0.86 (0.82) for the filter measurements of Cl?, NO3?, SO42? and NH4+, respectively. A HONO comparison with a batch denuder shows large scatter (R2 = 0.41). The MARGA HNO3 is underestimated compared to a batch and coated denuder with shorter inlets (slopes of 0.16 and 0.08, respectively). Less NH3 was observed in coated denuders for high ambient concentrations. Long-time measurements show clear daily and seasonal variabilities. Potential Source Contribution Function (PSCF) analysis indicates the emission area of particulate ions Cl?, NO3?, SO42?, NH4+, K+ and gaseous SO2 to lie in eastern European countries, predominantly in wintertime. Coarse mode sea salt particles are transported from the North Sea to Melpitz. The particles at Melpitz are nearly neutralised with a mean molar ratio of 0.90 for the five-year study. A slight increase of the neutralization ratio over the last three years indicates a stronger decrease of the anthropogenically emitted NO3? and SO42? compared to NH4+.
期刊介绍:
The Journal of Atmospheric Chemistry is devoted to the study of the chemistry of the Earth''s atmosphere, the emphasis being laid on the region below about 100 km. The strongly interdisciplinary nature of atmospheric chemistry means that it embraces a great variety of sciences, but the journal concentrates on the following topics:
Observational, interpretative and modelling studies of the composition of air and precipitation and the physiochemical processes in the Earth''s atmosphere, excluding air pollution problems of local importance only.
The role of the atmosphere in biogeochemical cycles; the chemical interaction of the oceans, land surface and biosphere with the atmosphere.
Laboratory studies of the mechanics in homogeneous and heterogeneous transformation processes in the atmosphere.
Descriptions of major advances in instrumentation developed for the measurement of atmospheric composition and chemical properties.