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Long-term (2001–2012) trends of carbonaceous aerosols from a remote island in the western North Pacific: an outflow region of Asian pollutants

机译:北太平洋西部偏远岛的长期(2001-2012)碳质气溶胶趋势:亚洲污染物的流出区域

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The present study reports on long-term trends of carbonaceous aerosols in total suspended particulate (TSP) samples collected at Chichijima in the western North Pacific during 2001–2012. Seasonal variations of elemental carbon (EC), organic carbon (OC), and water-soluble organic carbon (WSOC) concentrations showed maxima in winter to spring and minima in summer. These seasonal differences in the concentrations of carbonaceous aerosols were associated with the outflows of polluted air masses from East Asia, which are clearly distinguishable from pristine air masses from the central Pacific. The higher concentrations of carbonaceous aerosols during winter to spring are associated with long-range atmospheric transport of East Asian continental polluted air masses, whereas lower concentrations may be due to pristine air masses from the central Pacific in summer. The annual trends of OC?∕?EC (+0.46?%?yr?1), WSOC (+0.18?%?yr?1) and WSOC?∕?OC (+0.08?%?yr?1) showed significant (p????0.05) increases during the period of 2001–2012, suggesting that photochemical formation of WSOC and its contributions to secondary organic aerosols (SOAs) have increased over the western North Pacific via long-range atmospheric transport. We found a significant increase (+0.33?%?yr?1) in nss-K+?∕?EC ratios, demonstrating that concentrations of biomass-burning-derived carbonaceous aerosols have increased, while those of primary fossil-fuel-derived aerosols have decreased over the western North Pacific. Further, secondary biogenic emissions are also important over the western North Pacific as inferred from a significant increase (+0.14?%?yr?1) in the concentrations of methanesulfonate (MSA?, a tracer for biogenic sources). This point was further supported by a moderate correlation (r?=?0.40) between WSOC and MSA?. We also found a significant increase in OC?∕?TC (total carbon) and WSOC?∕?TC ratios, further suggesting that photochemical formation of WSOC and its contributions to SOAs have increased over the western North Pacific during 2001–2012 via long-range atmospheric transport from East Asia.
机译:本研究报告了2001 - 2012年西北太平洋在北太平洋西部Chichijima收集的总悬浮颗粒(TSP)样品中碳质气溶胶的长期趋势。元素碳(EC),有机碳(OC)和水溶性有机碳(WSOC)浓度的季节性变化在冬季冬季显示了最大的Maxima。这些碳质气溶胶浓度的季节性差异与来自东亚的污染空气群众的流出有关,这些空气群众从中部地区的原始空气群众明显区别。冬季含有较高浓度的碳质气溶胶到春天与东亚大陆污染空气群众的远程大气运输有关,而较低的浓度可能是由于夏季中央太平洋的原始空气群众。 oc的年趋势?/?eC(+0.46?%?Yr?1),WSOC(+0.18?%?YR?1)和WSOC?oc(+0.08?%?YR?1)显示出显着( P ???? 0.05)在2001 - 2012年期间增加,表明WSOC的光化学形成及其对二次有机气溶胶(SOA)的贡献通过远程大气运输,在西北太平洋方面增加了。在NSS-K + + /α/α的比率中发现了显着增加(+0.33?%?YR?1),证明了生物质燃烧衍生的碳质气溶胶的浓度增加,而原发性化石燃料衍生的气溶胶具有在西北太平洋西部减少。此外,二次生物排放在西北太平洋中也重要,从甲磺酸盐浓度(MSA磺酸盐浓度(MSA〜2,生物源的示踪剂)中推断出来。通过WSOC和MSA之间的中等相关性(R?= 0.40)进一步支持该点?我们还发现OC的显着增加(总碳)和WSOC?/?TC比率,进一步表明WSOC的光化学形成及其对SOA的贡献在2001 - 2012年期间通过长期增加了西北太平洋来自东亚的大气运输范围。

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