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Seasonal variations in aerosol particle composition at the puy-de-D?me research station in France

机译:Puy-de-d的气溶胶颗粒组成的季节变异?ME在法国的研究站

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Detailed investigations of the chemical and microphysical properties of atmospheric aerosol particles were performed at the puy-de-D?me (pdD) research station (1465 m) in autumn (September and October 2008), winter (February and March 2009), and summer (June 2010) using a compact Time-of-Flight Aerosol Mass Spectrometer (cToF-AMS). Over the three campaigns, the average mass concentrations of the non-refractory submicron particles ranged from 10 μg m3 up to 27 μg m3. Highest nitrate and ammonium mass concentrations were measured during the winter and during periods when marine modified airmasses were arriving at the site, whereas highest concentrations of organic particles were measured during the summer and during periods when continental airmasses arrived at the site. The measurements reported in this paper show that atmospheric particle composition is strongly influenced by both the season and the origin of the airmass. The total organic mass spectra were analysed using positive matrix factorisation to separate individual organic components contributing to the overall organic particle mass concentrations. These organic components include a low volatility oxygenated organic aerosol particle (LV-OOA) and a semi-volatile organic aerosol particle (SV-OOA). Correlations of the LV-OOA components with fragments of m/z 60 and m/z 73 (mass spectral markers of wood burning) during the winter campaign suggest that wintertime LV-OOA are related to aged biomass burning emissions, whereas organic aerosol particles measured during the summer are likely linked to biogenic sources. Equivalent potential temperature calculations, gas-phase, and LIDAR measurements define whether the research site is in the planetary boundary layer (PBL) or in the free troposphere (FT)/residual layer (RL). We observe that SV-OOA and nitrate particles are associated with air masses arriving from the PBL where as particle composition measured from RL/FT airmasses contain high mass fractions of sulphate and LV-OOA. This study provides unique insights into the effects of season and airmass variability on regional aerosol particles measured at an elevated site.
机译:在Puy-de-d?Me(PDD)研究站(2008年9月和2008年9月),冬季(2009年2月)和夏季(2010年6月)使用紧凑的飞行时间气溶胶质谱仪(CTOF-AMS)。在三个竞选中,非耐火亚微米颗粒的平均质量浓度范围为10μgm3,高达27μgm3。在冬季测量最高的硝酸盐和铵质量浓度,期间在船舶到达现场时,虽然夏季,但在夏季,当欧式气候达到现场时,测量最高浓度的有机颗粒。本文报道的测量表明,大气颗粒组成受到空气司司季节和起源的强烈影响。使用阳性基质分子分析总有机质谱以分离有助于整体有机颗粒质量浓度的单独有机组分。这些有机组分包括低挥发性含氧有机气溶胶颗粒(LV-OOA)和半挥发性有机气溶胶颗粒(SV-OOA)。冬季运动期间M / Z 60和M / Z 73碎片的LV-OOA组分的相关性表明,冬季LV-OOA与年龄的生物质燃烧排放有关,而测量有机气溶胶颗粒在夏天可能与生物来源有关。等效潜在的温度计算,气相和激光雷达测量定义了研究现场是否在行星边界层(PBL)中或在自由的对流层(FT)/残余层(RL)中。我们观察到SV-OOA和硝酸盐颗粒与从PBL到达的空气质量相关,其中从RL / FT气体测量的颗粒组合物含有高硫酸盐和LV-OOA。本研究提供了对在升高部位测量的季节气溶胶颗粒上的季节和空气变异性的独特见解。

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