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Summertime surface PMsub1/sub aerosol composition and size by source region at the Lampedusa island in the central Mediterranean Sea

机译:夏季表面PM 1 气溶胶组成和灯具区域在中央地中海的灯罩岛源区

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摘要

Measurements of aerosol composition and size distributions were taken duringthe summer of 2013 at the remote island of Lampedusa in the southern centralMediterranean Sea. These measurements were part of the ChArMEx/ADRIMED(Chemistry and Aerosol Mediterranean Experiment/Aerosol Direct RadiativeForcing on the Mediterranean Climate) framework and took place duringSpecial Observation Period 1a (SOP-1a) from 11 June to 5 July 2013. From compact time-of-flight aerosol mass spectrometer (cToF-AMS)measurements in the size range below 1 µm in aerodynamic diameter(PM1), particles were predominately comprised of ammonium and sulfate. Onaverage, ammonium sulfate contributed 63 % to the non-refractory PM1mass, followed by organics (33 %). The organic aerosol was generally veryhighly oxidized (f44 values were typically between 0.25 and 0.26). Thecontribution of ammonium sulfate was generally higher than organic aerosolin comparison to measurements taken in the western Mediterranean but isconsistent with studies undertaken in the eastern basin. Source apportionment of organics using a statistical (positive matrixfactorization) model revealed four factors: a hydrocarbon-like organicaerosol (HOA), a methanesulfonic-acid-related oxygenated organic aerosol(MSA-OOA), a more oxidized oxygenated organic aerosol (MO-OOA) and a lessoxidized oxygenated organic aerosol (LO-OOA). The MO-OOA was thedominant factor for most of the campaign (53 % of the PM1 OA mass). It waswell correlated with SO42-, highly oxidized and generally moredominant during easterly air masses originating from the easternMediterranean and central Europe. The LO-OOA factor had a very similarcomposition to the MO-OOA factor but was more prevalent during westerlywinds, with air masses originating from the Atlantic Ocean, the westernMediterranean and at high altitudes over France and Spain from mistralwinds. The MSA-OOA factor contributed an average 12 % to the PM1 OA andwas more dominant during the mistral winds. The HOA, representing observedprimary organic aerosol, only contributed 8 % of the average PM1 OA duringthe campaign. Even though Lampedusa is one of the most remote sites in the Mediterranean,PM1 concentrations (10 ± 5 µg m−3) were comparable to thoseobserved in coastal cities and sites closer to continental Europe. Cleanerconditions corresponded to higher wind speeds. Nucleation and growth of newaerosol particles was observed during periods of north-westerly winds. From aclimatology analysis from 1999 to 2012, these periods were much moreprevalent during the measurement campaign than during the preceding 13 years.These results support previous findings that highlight the importanceof different large-scale synoptic conditions in determining the regional andlocal aerosol composition and oxidation and also suggest that a non-pollutedsurface atmosphere over the Mediterranean is rare.
机译:气溶胶成分和粒度分布的测量是在2013年夏天duringthe在兰佩杜萨南部centralMediterranean海上孤岛。这些测量结果(化学与气溶胶地中海实验/气溶胶直接RadiativeForcing地中海气候)框架ChArMEx / ADRIMED的一部分,发生duringSpecial观察周期1A(SOP-1A)从6月11日至2013年5月从紧凑的时间的的尺寸范围内小于1微米的中值空气动力学直径(PM1) - 飞行气溶胶质谱仪(cToF-AMS)的测量,粒子主要由铵和硫酸的。 Onaverage,硫酸铵贡献63%到非耐火PM1mass,随后有机物(33%)。将有机气溶胶通常veryhighly氧化(F44值分别通常为0.25和0.26之间)。硫酸铵Thecontribution一般比有机aerosolin相比,在地中海西部进行测量,但在盆地东部进行的研究isconsistent更高。使用统计(正matrixfactorization)模型有机物源解析揭示四个因素:烃类organicaerosol(HOA),一甲酸有关的含氧有机气溶胶(MSA-OOA),更氧化的含氧有机气溶胶(MO-OOA )和lessoxidized含氧有机气溶胶(LO-OOA)。该MO-OOA对于大多数运动(PM1的质量OA的53%)的thedominant因素。它waswell从easternMediterranean和欧洲中部偏东气团始发期间SO42-相关,高度氧化和一般moredominant。在LO-OOA因素westerlywinds过程中有一个非常similarcomposition到MO-OOA因素,但较普遍,与来自大西洋,westernMediterranean气团始发和在高海拔超过法国和西班牙从mistralwinds。在MSA-OOA因子贡献的平均12%至PM1 OA andwas在西北风的风更占优势。的110A,表示observedprimary有机气溶胶,只贡献平均PM1 OA的8%duringthe运动。即使兰佩杜萨是地中海最远程站点中的一个,PM1浓度(10±5微克M-3)分别相当于在沿海城市和位点更靠近欧洲大陆thoseobserved。 Cleanerconditions对应更高的风速。成核和newaerosol颗粒的生长过程中西北风的时期进行了观察。从aclimatology分析1999年至2012年,这些周期比在前述13个years.These结果支持以前的发现,即突出importanceof不同大规模天气条件在确定区域andlocal气溶胶组合物和氧化,并且还测量活动期间多moreprevalent建议非pollutedsurface气氛地中海的是罕见的。

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