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首页> 外文期刊>Atmospheric environment >Airborne investigation of the aerosols-cloud interactions in the vicinity and within a marine stratocumulus over the North Sea during EUCAARI (2008)
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Airborne investigation of the aerosols-cloud interactions in the vicinity and within a marine stratocumulus over the North Sea during EUCAARI (2008)

机译:EUCAARI(2008)期间对北海附近和海洋平流积云内气溶胶-云相互作用的空中研究。

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摘要

Within the European Aerosol Cloud Climate and Air Quality Interactions (EUCAARI) project, the Meteo France research aircraft ATR-42 was operated from Rotterdam (Netherlands) airport during May 2008, to perform scientific flights dedicated to the investigation of aerosol-cloud interactions. The objective of this study is to illustrate the impact of cloud processing on the aerosol particle physical and chemical properties. The presented results are retrieved from measurements during flight operation with two consecutive flights, first from Rotterdam to Newcastle (United Kingdom) and subsequently reverse along the same waypoints back to Rotterdam using data measured with compact Time of Flight Aerosol Mass Spectrometer (cToF-AMS) and Scanning Mobility Particle Sizer (SMPS). Cloud-related measurements during these flights were performed over the North Sea within as well as in close vicinity of a marine stratocumulus cloud layer. Particle physical and chemical properties observed in the close vicinity, below and above the stratocumulus cloud, show strong differences: (1) the averaged aerosol size distributions, observed above and below the cloud layer, are of bimodal character with pronounced minima between Aitken and accumulation mode, very likely due to cloud processing. (2) the chemical composition of aerosol particles is strongly dependent on the position relative to the cloud layer (vicinity or below/above cloud). In general, the nitrate and organic relative mass fractions decrease with decreasing distance to the cloud, in the transit from cloud-free conditions towards the cloud boundaries. This relative mass fraction decrease ranges from a factor of three to ten, thus leading to an increase of the sulfate and ammonium relative mass concentrations while approaching the cloud layer. (3), the chemical composition of cloud droplet residuals, analyzed downstream of a Counterflow virtual Impactor (CVI) inlet indicates increased fractions of mainly soluble chemical compounds such as nitrate and organics, compared to non cloud processed particles. Finally, a net overbalance of nitrate aerosol has been revealed by comparing cloud droplet residual and non cloud processed aerosol chemical compositions. Conclusively, this study highlights gaps concerning the sampling strategy that need to be addressed for the future missions.
机译:在欧洲气溶胶云气候与空气质量相互作用(EUCAARI)项目中,法国气象卫星研究飞机ATR-42在2008年5月从鹿特丹(荷兰)机场运行,进行了专门研究气溶胶-云相互作用的科学飞行。这项研究的目的是说明云处理对气溶胶颗粒物理和化学性质的影响。在连续两次飞行的飞行操作过程中,从测量结果中检索出结果,首先是从鹿特丹到纽卡斯尔(英国),然后使用紧凑的飞行时间气溶胶质谱仪(cToF-AMS)沿相同的航路点返回鹿特丹。和扫描迁移率粒度仪(SMPS)。在这些飞行过程中,与云有关的测量是在北海以及海洋平积云层附近进行的。在层状积云附近,上方和下方观察到的粒子物理和化学性质显示出很强的差异:(1)在云层上方和下方观察到的平均气溶胶粒径分布具有双峰特征,在艾肯和积聚之间具有明显的最小值模式,很可能是由于云处理。 (2)气溶胶颗粒的化学成分在很大程度上取决于相对于云层的位置(附近或云层上方/上方)。通常,在从无云条件向云边界过渡的过程中,硝酸盐和有机物的相对质量分数随与云的距离减小而降低。该相对质量分数的降低范围是三倍至十倍,因此导致硫酸盐和铵的相对质量浓度在接近云层时增加。 (3),在逆流虚拟撞击器(CVI)入口的下游分析了云滴残留物的化学成分,与未经云处理的颗粒相比,主要溶解性化合物(如硝酸盐和有机物)的分数增加了。最后,通过比较云滴残留物和未经云处理的气溶胶化学成分,揭示了硝酸盐气溶胶的净过剩。总之,本研究突出了与未来任务有关的采样策略方面的空白。

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  • 来源
    《Atmospheric environment》 |2013年第12期|288-303|共16页
  • 作者单位

    Laboratoire de Meteorologie Physique, CNRS, Universite Blaise Pascal, UMR6016, Aubiere cedex, France,NASA Langley Research Center, Hampton, VA 23666, USA,NASA Langley Research Center, 21 Langley Blvd, MS 483, Bldg 1250, Room 125, Hampton, VA 23681, USA;

    Laboratoire de Meteorologie Physique, CNRS, Universite Blaise Pascal, UMR6016, Aubiere cedex, France,Institute for Physics of the Atmosphere, Johannes Gutenberg University, Mainz, Germany;

    Laboratoire de Meteorologie Physique, CNRS, Universite Blaise Pascal, UMR6016, Aubiere cedex, France;

    Centre National de Recherches Meteorologiques, URA 1357, Meteo-France, Toulouse, France;

    Centre National de Recherches Meteorologiques, URA 1357, Meteo-France, Toulouse, France;

    Norwegian Institute for Air Research, Kjeller, Norway;

    Laboratoire de Meteorologie Physique, CNRS, Universite Blaise Pascal, UMR6016, Aubiere cedex, France,Departement of Atmospheric and Oceanic Sciences, McGill University, Montreal, Canada;

    Centre National de Recherches Meteorologiques, URA 1357, Meteo-France, Toulouse, France;

    Centre National de Recherches Meteorologiques, URA 1357, Meteo-France, Toulouse, France;

    Centre National de Recherches Meteorologiques, URA 1357, Meteo-France, Toulouse, France,Laboratoire des Science du Climat et de l'Environnement, CNRS, France;

    Centre National de Recherches Meteorologiques, URA 1357, Meteo-France, Toulouse, France;

    Laboratoire de Glaciologie et Geophysique de l'Environnement, UMR 5183, Universite de Grenoble 1/CNRS, Grenoble, France;

    Centre National de Recherches Meteorologiques, URA 1357, Meteo-France, Toulouse, France;

    Centre National de Recherches Meteorologiques, URA 1357, Meteo-France, Toulouse, France;

    Laboratoire de Meteorologie Physique, CNRS, Universite Blaise Pascal, UMR6016, Aubiere cedex, France;

    Laboratoire de Meteorologie Physique, CNRS, Universite Blaise Pascal, UMR6016, Aubiere cedex, France;

    Laboratoire de Meteorologie Physique, CNRS, Universite Blaise Pascal, UMR6016, Aubiere cedex, France;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Aerosols; CCN; In-situ measurements; Stratocumulus; Activation;

    机译:气溶胶;CCN;现场测量;层积云;激活;

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