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Source attribution of climatically important aerosol properties measured at Paposo (Chile) during VOCALS

机译:在VOCALS期间在波波索(智利)测量的气候重要气溶胶特性的来源归因

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pstrongAbstract./strong Measurements of submicron aerosol composition, light scattering, and size distribution were made from 17 October to 15 November 2008 at the elevated Paposo site (25?° 0.4' S, 70?° 27.01' W, 690 m a.s.l.) on the Chilean coast as part of the VOCALS* Regional Experiment (REx). Based on the chemical composition measurements, a receptor modeling analysis using Positive Matrix Factorization (PMF) was carried out, yielding four broad source categories of the aerosol mass, light scattering coefficient, and a proxy for cloud condensation nucleus (CCN) concentration at 0.4% supersaturation derived from the size distribution measurements assuming an observed soluble mass fraction of 0.53. The sources resolved were biomass burning, marine, an urban-biofuels mix and a somewhat ambiguous mix of smelter emissions and mineral dust. The urban-biofuels mix is the most dominant aerosol mass component (52%) followed by biomass burning (25%), smelter/soil dust (12%) and marine (9%) sources. The average (mean?±std) submicron aerosol mass concentration, aerosol light scattering coefficient and proxy CCN concentration were, 8.77?±5.40 ??g msup−3/sup, 21.9?±11.0 Mmsupa??1/sup and 548?±210 cmsupa??3/sup, respectively. Sulfate is the dominant identified submicron species constituting roughly 40% of the dry mass (3.64?±2.30 ??g msup−3/sup), although the indentified soluble species constitute only 53% of the mass. Much of the unidentified mass is likely organic in nature. The relative importance of each aerosol source category is different depending upon whether mass, light scattering, or CCN concentration is being considered, indicating that the mean size of aerosols associated with each source are different. Marine aerosols do not appear to contribute to more than 10% to either mass, light scattering, or CCN concentration at this site. Back trajectory cluster analysis proved consistent with the PMF source attribution. brbr *VOCALS VAMOS** Ocean-Cloud-Atmosphere-Land Study (VOCALS) brbr **VAMOS Variability of American Monsoon System/p.
机译:> >摘要。从2008年10月17日至11月15日,在高位的Paposo站点(25?°0.4'S,70?°27.01)进行了亚微米气溶胶成分,光散射和尺寸分布的测量。作为VOCALS *区域实验(REx)的一部分,位于智利海岸690 m asl)。根据化学成分测量,使用正矩阵分解(PMF)进行了受体建模分析,得出了气溶胶质量,光散射系数和0.4%的云凝结核(CCN)浓度的四个主要来源类别。假设观察到的可溶质量分数为0.53,则从尺寸分布测量得出过饱和。解决的来源是生物质燃烧,海洋,城市生物燃料混合以及冶炼厂排放物和矿物粉尘的含混不清。城市生物燃料的混合是最主要的气溶胶质量成分(52%),其次是生物质燃烧(25%),冶炼厂/土壤粉尘(12%)和海洋(9%)来源。亚微米气溶胶的平均浓度(平均值±std),气溶胶光散射系数和代理CCN浓度分别为8.77±5.40 g·mg减-3、21.9±11.0 Mm·a分别为?? 1 和548?±210 cm a ?? 3 。硫酸盐是确定的占主导地位的亚微米物质,约占干燥质量的40%(3.64?±2.30 g g m s负3),尽管确定的可溶物质仅占质量的53%。本质上,许多未知的物质很可能是有机的。根据是否考虑质量,光散射或CCN浓度,每种气溶胶来源类别的相对重要性都不同,这表明与每种来源相关的气溶胶的平均大小是不同的。在该位置,海洋气溶胶对质量,光散射或CCN浓度的贡献似乎均不超过10%。反向轨迹聚类分析证明与PMF源归因一致。 * VOCALS VAMOS **海洋-云-大气-陆地研究(VOCALS) **美国季风系统的VAMOS变异性

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