Global S&T Development Trend Analysis Platform of Resources and Environment
DOI | 10.5194/acp-17-2817-2017 |
Phenomenology of high-ozone episodes in NE Spain | |
Querol, Xavier1; Gangoiti, Gotzon2; Mantilla, Enrique3; Alastuey, Andres1; Cruz Minguillon, Maria1; Amato, Fulvio1; Reche, Cristina1; Viana, Mar1; Moreno, Teresa1; Karanasiou, Angeliki1; Rivas, Ioar1; Perez, Noemi1; Ripoll, Anna1; Brines, Mariola1; Ealo, Marina1; Pandolfi, Marco1; Lee, Hong-Ku4; Eun, Hee-Ram4; Park, Yong-Hee4; Escudero, Miguel5; Beddows, David6; Harrison, Roy M.6,9; Bertrand, Amelie7; Marchand, Nicolas7; Lyasota, Andrei8; Codina, Bernat8; Olid, Miriam8; Udina, Mireia8; Jimenez-Esteve, Bernat8; Soler, Maria R.8; Alonso, Lucio2; Millan, Millan3; Ahn, Kang-Ho4 | |
2017-02-23 | |
发表期刊 | ATMOSPHERIC CHEMISTRY AND PHYSICS
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ISSN | 1680-7316 |
EISSN | 1680-7324 |
出版年 | 2017 |
卷号 | 17期号:4 |
文章类型 | Article |
语种 | 英语 |
国家 | Spain; South Korea; England; France; Saudi Arabia |
英文摘要 | Ground-level and vertical measurements (performed using tethered and non-tethered balloons), coupled with modelling, of ozone (O-3), other gaseous pollutants (NO, NO2, CO, SO2) and aerosols were carried out in the plains (Vic Plain) and valleys of the northern region of the Barcelona metropolitan area (BMA) in July 2015, an area typically recording the highest O-3 episodes in Spain. Our results suggest that these very high O-3 episodes were originated by three main contributions: (i) the surface fumigation from high O-3 reservoir layers located at 1500-3000m a.g.l. (according to modelling and non-tethered balloon measurements), and originated during the previous day(s) injections of polluted air masses at high altitude; (ii) local/regional photochemical production and transport (at lower heights) from the BMA and the surrounding coastal settlements, into the inland valleys; and (iii) external (to the study area) contributions of both O-3 and precursors. These processes gave rise to maximal O-3 levels in the inland plains and valleys northwards from the BMA when compared to the higher mountain sites. Thus, a maximum O-3 concentration was observed within the lower tropospheric layer, characterised by an upward increase of O-3 and black carbon (BC) up to around 100-200m a.g.l. (reaching up to 300 mu g m(-3) of O-3 as a 10 s average), followed by a decrease of both pollutants at higher altitudes, where BC and O-3 concentrations alternate in layers with parallel variations, probably as a consequence of the atmospheric transport from the BMA and the return flows (to the sea) of strata injected at certain heights the previous day(s). At the highest altitudes reached in this study with the tethered balloons (900-1000m a.g.l.) during the campaign, BC and O-3 were often anti-correlated or unrelated, possibly due to a prevailing regional or even hemispheric contribution of O-3 at those altitudes. In the central hours of the days a homogeneous O-3 distribution was evidenced for the lowest 1 km of the atmosphere, although probably important variations could be expected at higher levels, where the high O-3 return strata are injected according to the modelling results and non-tethered balloon data. Relatively low concentrations of ultrafine particles (UFPs) were found during the study, and nucleation episodes were only detected in the boundary layer. Two types of O-3 episodes were identified: type A with major exceedances of the O-3 information threshold (180 mu g m(-3) on an hourly basis) caused by a clear daily concatenation of local/regional production with accumulation (at upper levels), fumigation and direct transport from the BMA (closed circulation); and type B with regional O-3 production without major recirculation (or fumigation) of the polluted BMA/regional air masses (open circulation), and relatively lower O-3 levels, but still exceeding the 8 h averaged health target. To implement potential O-3 control and abatement strategies two major key tasks are proposed: (i) meteorological forecasting, from June to August, to predict recirculation episodes so that NOx and VOC abatement measures can be applied before these episodes start; (ii) sensitivity analysis with high-resolution modelling to evaluate the effectiveness of these potential abatement measures of precursors for O-3 reduction. |
领域 | 地球科学 |
收录类别 | SCI-E |
WOS记录号 | WOS:000395109900004 |
WOS关键词 | WESTERN MEDITERRANEAN BASIN ; PHOTOCHEMICAL AIR-POLLUTION ; ATMOSPHERIC PROCESSES ; SOURCE APPORTIONMENT ; TROPOSPHERIC OZONE ; IBERIAN PENINSULA ; CLIMATE-CHANGE ; AREA ; TRANSPORT ; DYNAMICS |
WOS类目 | Environmental Sciences ; Meteorology & Atmospheric Sciences |
WOS研究方向 | Environmental Sciences & Ecology ; Meteorology & Atmospheric Sciences |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | http://119.78.100.173/C666/handle/2XK7JSWQ/30442 |
专题 | 地球科学 |
作者单位 | 1.CSIC, IDAEA, Inst Environm Assessment & Water Res, C Jordi Girona 18-26, ES-08034 Barcelona, Spain; 2.Univ Pais Vasco UPV EHU, Dept Ingn Quim & Medio Ambiente, Escuela Tecn Super Ingn Bilbao, Urkixo Zumarkalea S-N, Bilbao 48013, Spain; 3.CSIC, Unidad Asociada, CEAM, Parque Tecnol C Charles R Darwin 14, Valencia 46980, Spain; 4.Hanyang Univ, Dept Mech Engn, Ansan 425791, South Korea; 5.Acad Gen Mil, Ctr Univ Def Zaragoza, Ctra Huesca S-N, Zaragoza 50090, Spain; 6.Univ Birmingham, Div Environm Hlth & Risk Management, Sch Geog Earth & Environm Sci, Birmingham B15 2TT, W Midlands, England; 7.Aix Marseille Univ, CNRS, LCE, F-13331 Marseille, France; 8.Univ Barcelona, Fac Phys, Dept Astron & Meteorol, Marti i Franques 1, E-08028 Barcelona, Spain; 9.King Abdulaziz Univ, Ctr Excellence Environm Studies, Dept Environm Sci, Jeddah, Saudi Arabia |
推荐引用方式 GB/T 7714 | Querol, Xavier,Gangoiti, Gotzon,Mantilla, Enrique,et al. Phenomenology of high-ozone episodes in NE Spain[J]. ATMOSPHERIC CHEMISTRY AND PHYSICS,2017,17(4). |
APA | Querol, Xavier.,Gangoiti, Gotzon.,Mantilla, Enrique.,Alastuey, Andres.,Cruz Minguillon, Maria.,...&Ahn, Kang-Ho.(2017).Phenomenology of high-ozone episodes in NE Spain.ATMOSPHERIC CHEMISTRY AND PHYSICS,17(4). |
MLA | Querol, Xavier,et al."Phenomenology of high-ozone episodes in NE Spain".ATMOSPHERIC CHEMISTRY AND PHYSICS 17.4(2017). |
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