Anthropogenic fine aerosols dominate the wintertime regime over the northern Indian Ocean

K. Budhavant, S. Bikkina, A. Andersson, E. Asmi, J. Backman, Jutta Kesti, H. Zahid, S. Satheesh, Ö. Gustafsson
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引用次数: 19

Abstract

Abstract This study presents and evaluates the most comprehensive set to date of chemical, physical and optical properties of aerosols in the outflow from South Asia covering a full winter (Nov. 2014 – March 2015), here intercepted at the Indian Ocean receptor site of the Maldives Climate Observatory in Hanimaadhoo (MCOH). Cluster analysis of air-mass back trajectories for MCOH, combined with AOD and meteorological data, demonstrate that the wintertime northern Indian Ocean is strongly influenced by aerosols transported from source regions with three major wind regimes, originating from the Indo-Gangetic Plain (IGP), the Bay of Bengal (BoB) and the Arabian Sea (AS). As much as 97 ± 3% of elemental carbon (EC) in the PM10 was also found in the fine mode (PM2.5). Other mainly anthropogenic constituents such as organic carbon (OC), non-sea-salt (nss) -K+, nss-SO42− and NH4+ were also predominantly in the fine mode (70–95%), particularly in the air masses from IGP. The combination at this large-footprint receptor observatory of consistently low OC/EC ratio (2.0 ± 0.5), strong linear relationships between EC and OC as well as between nss-K+ and both OC and EC, suggest a predominance of primary sources, with a large biomass burning contribution. The particle number-size distributions for the air masses from IGP and BoB exhibited clear bimodal shapes within the fine fraction with distinct accumulation (0.1 μm < d < 1 μm) and Aitken (0.025 μm < d < 0.10 μm) modes. This study also supports that IGP is a key source region for the wider South Asia and nearby oceans, as defined by the criteria that anthropogenic AODs exceed 0.3 and absorption AOD > 0.03. Taken together, the aerosol pollution over the northern Indian Ocean in the dry season is dominated by a well-mixed long-range transported regime of the fine-mode aerosols largely from primary combustion origin.
在北印度洋上空,人为的细小气溶胶主导着冬季状态
本研究介绍并评估了迄今为止最全面的一组南亚外流气溶胶的化学、物理和光学特性,涵盖了整个冬季(2014年11月- 2015年3月),这些气溶胶在马尔代夫气候观测站位于哈尼马杜(MCOH)的印度洋受体站点拦截。结合AOD和气象数据,对MCOH气团反轨迹的聚类分析表明,冬季北印度洋受到来自印度-恒河平原(IGP)、孟加拉湾(BoB)和阿拉伯海(AS)三种主要风源区域输送的气溶胶的强烈影响。在细颗粒物(PM2.5)中,PM10中元素碳(EC)的含量也高达97±3%。其他主要人为成分如有机碳(OC)、非海盐(nss) -K+、nss- so42−和NH4+也以细态为主(70-95%),特别是来自IGP的气团。在这个大足迹受体观测站,持续的低OC/EC比率(2.0±0.5),EC和OC之间以及nss-K+与OC和EC之间的强线性关系,表明主要来源占主导地位,其中生物质燃烧贡献很大。IGP和BoB气团的颗粒数-尺寸分布在细段内呈现明显的双峰型,具有明显的累积模式(0.1 μm < d < 1 μm)和艾特肯模式(0.025 μm < d < 0.10 μm)。根据人为AOD超过0.3和吸收AOD > 0.03的标准,本研究还支持IGP是更广泛的南亚和附近海洋的关键源区。综上所述,旱季北印度洋上空的气溶胶污染主要是由主要来自一次燃烧的细态气溶胶的混合良好的远程输送状态所主导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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