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The impacts of precursor reduction and meteorology on ground-level ozone in the Greater Toronto Area

机译:前驱物减少和气象学对大多伦多地区地面臭氧的影响

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摘要

Tropospheric ozone (O) is a major component of photochemical smog andis a known human health hazard, as well as a damaging factor for vegetation.Its precursor compounds, nitrogen oxides (NO) and volatile organiccompounds (VOCs), have a variety of anthropogenic and biogenic sources andexhibit non-linear effects on ozone production. As an update to previousstudies on ground-level ozone in the Greater Toronto Area (GTA), we presentan analysis of NO, VOC and O data from federal and provincialgovernmental monitoring sites in the GTA from 2000 to 2012. We show that, overthe study period, summertime 24 h VOC reactivity and NO midday(11:00–15:00) concentrations at all sites decreased significantly; since2000, all sites experienced a decrease in NO of 28–62% and inmeasured VOC reactivity of at least 53–71%. Comparing 2002–2003 to2011–2012, the summed reactivity of OH towards NO and a suite ofmeasured VOCs decreased from 8.6 to 4.6 s. Ratios of reactiveVOC pairs indicate that the effective OH concentration experienced byprimary pollutants in the GTA has increased significantly over the studyperiod. Despite the continuous decrease in precursor levels, ozoneconcentrations are not following the same pattern at all stations; it wasfound that the Canada-wide Standard for ozone continues to be exceeded atall monitoring stations. Additionally, while the years 2008–2011 hadconsistently lower ozone levels than previous years, 2012 experienced one ofthe highest recorded summertime ozone concentrations and a large number ofsmog episodes. We demonstrate that these high ozone observations in 2012 maybe a result of the number of days with high solar radiation, the number ofstagnant periods and the transport of high ozone levels from upwind regions.
机译:对流层臭氧(O)是光化学烟雾的主要成分,是已知的人类健康危害以及对植被的破坏因素,其前体化合物,氮氧化物(NO)和挥发性有机化合物(VOC)具有多种人为和有害物质。生物来源并表现出对臭氧生产的非线性影响。作为对大多伦多地区(GTA)地面臭氧的先前研究的更新,我们提出了2000年至2012年来自GTA联邦和省政府监测站点的NO,VOC和O数据的分析。我们表明,在研究期间,夏季所有地点的24小时VOC反应性和中午(11:00-15:00)的NO浓度均显着下降;自2000年以来,所有站点的NO降低了28-62%,测得的VOC反应性至少达到了53-71%。与2002–2003年至2011–2012年相比,OH对NO的总反应性和一系列测得的VOC从8.6 s下降到4.6 s。反应性VOC对的比率表明,在整个研究期间,GTA中主要污染物经历的有效OH浓度已显着增加。尽管前体水平不断下降,但所有站的臭氧浓度并没有遵循相同的模式。据发现,所有监测站的臭氧标准都继续超出加拿大范围。此外,虽然2008-2011年的臭氧水平一直低于往年,但2012年的夏季臭氧浓度和大量烟雾事件是有记录以来最高的之一。我们证明,2012年这些较高的臭氧观测值可能是由于太阳辐射高的天数,停滞期的数量以及来自上风地区的高臭氧水平的输送所致。

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