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On the nature of sea salt aerosol at a coastal megacity: Insights from Manila, Philippines in Southeast Asia

机译:关于海盐气溶胶的性质,在沿海特征:来自菲律宾在东南亚马尼拉的见解

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摘要

This study utilizes multiple aerosol datasets collected in Metro Manila, Philippines to investigate sea salt aerosol characteristics. This coastal megacity allows for an examination of the impacts of precipitation and mixing of different air masses on sea salt properties, including overall concentration and size-resolved composition, hygroscopicity, and morphology. Intensive size-resolved measurements with a Micro-Orifice Uniform Deposit Impactor (MOUDI) between July-December 2018 revealed the following major results: (i) sea salt levels exhibit wide variability during the wet season, driven primarily by precipitation scavenging; (ii) ssNa(+) and Cl- peaked in concentration between 1.8 and 5.6 mu m, with Cl- depletion varying between 21.3 and 90.7%; (iii) mixing of marine and anthropogenic air masses yielded complex non-spherical shapes with species attached to the outer edges and Na+ uniformly distributed across particles unlike Cl-; (iv) there was significant contamination of sea salt aerosol by a variety of crustal and anthropogenic pollutants (Fe, Al, Ba, Mn, Pb, NO3-, V, Zn, NH4+); (v) categorization of samples in five different pollutant type categories (Background, Clean, Fire, Continental Pollution, Highest Rain) revealed significant differences in overall Cl- depletion with enhanced depletion in the submicrometer range versus the supermicrometer range; (vi) kappa values ranged from 0.02 to 0.31 with a bimodal profile across all stages, with the highest value coincident with the highest sea salt volume fraction in the 3.2-5.6 mu m stage, which is far lower than pure sea salt due to the significant influence of organics and black carbon. Analysis of longer term PM2.5 (particulate matter with aerodynamic diameter less than 2.5 mu m) and PMcoarse (= PM10 - PM2.5) data between August 2005 and October 2007 confirmed findings from the MOUDI data that more Cl- depletion occurred both in the wet season versus the dry season and on weekdays versus weekend days. This study demonstrates the importance of accounting for two factors in future studies on sea salt: (i) non-sea salt (nss) sources of Na+ impact calculations such as for Cl- depletion that typically assume that total Na+ concentration is derived from sa and (ii) considering precipitation data over a larger spatial domain rather than a point measurement at the study site to investigate wet scavenging.
机译:本研究利用了菲律宾地铁马尼拉地铁马尼拉的多个气溶胶数据集来研究海盐气溶胶特性。这种沿海特征允许检查不同空气质量对海盐性质的降水和混合的影响,包括整体浓度和尺寸分辨的组成,吸湿性和形态。 2018年7月至12月至12月12日至12月之间的微孔均匀沉积物(Moudi)的密集尺寸分辨测量揭示了以下主要结果:(i)海盐水平在潮湿的季节期间呈现广泛的变化,主要通过降水扫处理来驱动; (ii)SSNA(+)和浓度为1.8和5.6μm的CL-耗尽在21.3和90.7%之间变化; (iii)母船和人为气质的混合产生复杂的非球形形状,其物种与外边缘附着的物种和均匀分布在颗粒上不同于Cl-; (iv)各种地壳和人为污染物(Fe,Al,Ba,Mn,Pb,No3-,V,Zn,NH4 +),对海盐气溶胶污染的显着污染; (v)五种不同污染物类型类别的样品分类(背景,清洁,火,欧式污染,最高雨)揭示了在超级计量范围内具有增强的耗尽的整体CL-耗尽显着差异; (vi)κ值范围为0.02至0.31,所有阶段的双峰曲线均可,最高值与3.2-5.6 mu m阶段的最高海盐体积分数重合,这远远低于纯海盐有机物和黑碳的显着影响。延长术语PM2.5(具有空气动力直径小于2.5亩的颗粒物)和2005年8月至2007年10月之间的PMCOARSE(= PM10-PM2.5)数据确认了来自MOWI数据的调查结果,即在此中发生更多的CL-耗尽湿季与旱季和平日与周末日。本研究表明,在未来的海盐研究中核算了两个因素的重要性:(i)Na +抗冲击计算的非海盐(NSS)来源,例如通常假设总Na +浓度来自盐; (ii)考虑到更大的空间域中的降水数据而不是研究现场的点测量来调查湿扫失。

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  • 来源
    《Atmospheric environment》 |2019年第11期|116922.1-116922.14|共14页
  • 作者单位

    Univ Arizona Dept Chem & Environm Engn POB 210011 Tucson AZ 85721 USA;

    Univ Arizona Dept Chem & Environm Engn POB 210011 Tucson AZ 85721 USA;

    Univ Arizona Dept Chem & Environm Engn POB 210011 Tucson AZ 85721 USA;

    Manila Observ Quezon City 1101 Philippines|Ateneo Manila Univ Sch Sci & Engn Dept Phys Quezon City 1108 Philippines;

    Manila Observ Quezon City 1101 Philippines|Univ Philippines Inst Environm Sci & Meteorol Quezon City 1101 Philippines;

    Ateneo Manila Univ Sch Sci & Engn Dept Phys Quezon City 1108 Philippines;

    Manila Observ Quezon City 1101 Philippines|Ateneo Manila Univ Sch Sci & Engn Dept Phys Quezon City 1108 Philippines;

    Univ Arizona Dept Chem & Environm Engn POB 210011 Tucson AZ 85721 USA;

    Manila Observ Quezon City 1101 Philippines;

    Univ Arizona Dept Chem & Environm Engn POB 210011 Tucson AZ 85721 USA;

    Univ Arizona Dept Chem & Environm Engn POB 210011 Tucson AZ 85721 USA;

    Univ Calif Irvine Dept Civil & Environm Engn Irvine CA USA;

    Manila Observ Quezon City 1101 Philippines|Ateneo Manila Univ Sch Sci & Engn Dept Phys Quezon City 1108 Philippines;

    Univ Arizona Dept Chem & Environm Engn POB 210011 Tucson AZ 85721 USA;

    Univ Arizona Dept Chem & Environm Engn POB 210011 Tucson AZ 85721 USA|Univ Arizona Dept Hydrol & Atmospher Sci Tucson AZ 85721 USA;

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