Synoptic circulation patterns and local sources associated to high concentrations of tropospheric ozone in rural and suburban areas in southwestern Spain

2019 ◽  
Vol 13 (1) ◽  
pp. 97-108
Author(s):  
Maria Cerrato-Alvarez ◽  
Marcelino Núñez-Corchero ◽  
Conrado Miró-Rodríguez ◽  
Eduardo Pinilla-Gil
1993 ◽  
Vol 29 (10) ◽  
pp. 3303-3315 ◽  
Author(s):  
James P. Hughes ◽  
Dennis P. Lettenmaier ◽  
Peter Guttorp

2017 ◽  
Vol 17 (15) ◽  
pp. 9311-9332 ◽  
Author(s):  
Jihoon Seo ◽  
Jin Young Kim ◽  
Daeok Youn ◽  
Ji Yi Lee ◽  
Hwajin Kim ◽  
...  

Abstract. The air quality of the megacities in populated and industrialized regions like East Asia is affected by both local and regional emission sources. The combined effect of regional transport and local emissions on multiday haze was investigated through a synthetic analysis of PM2. 5 sampled at both an urban site in Seoul, South Korea and an upwind background site on Deokjeok Island over the Yellow Sea during a severe multiday haze episode in late February 2014. Inorganic components and carbonaceous species of daily PM2. 5 samples were measured, and gaseous pollutants, local meteorological factors, and synoptic meteorological conditions were also determined. A dominance of fine-mode particles (PM2. 5 ∕ PM10  ∼  0.8), a large secondary inorganic fraction (76 %), high OC ∕ EC (> 7), and highly oxidized aerosols (oxygen-to-carbon ratio of  ∼  0.6 and organic-mass-to-carbon ratio of  ∼  1.9) under relatively warm, humid, and stagnant conditions characterize the multiday haze episode in Seoul; however, the early and late stages of the episode show different chemical compositions of PM2. 5. High concentrations of sulfate in both Seoul and the upwind background in the early stage suggest a significant regional influence on the onset of the multiday haze. At the same time, high concentrations of nitrate and organic compounds in Seoul, which are local and highly correlated with meteorological factors, suggest the contribution of local emissions and secondary formation under stagnant meteorological conditions to the haze. A slow eastward-moving high-pressure system from southern China to the East China Sea induces the regional transport of aerosols and potential gaseous precursors for secondary aerosols from the North China Plain in the early stage but provides stagnant conditions conducive to the accumulation and the local formation of aerosols in the late stage. A blocking ridge over Alaska that developed during the episode hinders the zonal propagation of synoptic-scale systems and extends the haze period to several days. This study provides chemical insights into haze development sequentially by regional transport and local sources, and shows that the synoptic condition plays an important role in the dynamical evolution of long-lasting haze in the Asian continental outflow region.


2020 ◽  
Vol 20 (11) ◽  
pp. 2519-2528
Author(s):  
Ariadna Huerta-Viso ◽  
Javier Crespo ◽  
Nuria Galindo ◽  
Eduardo Yubero ◽  
Jose Francisco Nicolás

2016 ◽  
Author(s):  
Osamu Uchino ◽  
Tetsu Sakai ◽  
Toshiharu Izumi ◽  
Tomohiro Nagai ◽  
Isamu Morino ◽  
...  

Abstract. To validate products of the Greenhouse gases Observing SATellite (GOSAT), we observed vertical profiles of aerosols, thin cirrus clouds, and tropospheric ozone with a mobile lidar system that consisted of a two-wavelength (532 and 1064 nm) polarization lidar and a tropospheric ozone Differential Absorption Lidar (DIAL). We used these lidars to make continuous measurements over Saga (33.24° N, 130.29° E) during 20–31 March 2015. High ozone and high aerosol concentrations were observed almost simultaneously in the altitude range 0.5–1.5 km from 03:00 to 20:00 Japan Standard Time on 22 March 2015. The maximum ozone volume mixing ratio was ~ 110 ppbv. The maxima of the aerosol extinction coefficient and optical depth at 532 nm were 1.2 km−1 and 2.1, respectively. Backward trajectory analysis indicated that an air mass with high ozone and aerosol concentrations could have been transported from Northeast Asia. Based on the lidar data and the ground-based in-situ measurements at Saga, this air mass could have been transported to the surface by vertical mixing when the planetary boundary layer developed in the daytime. This plume, which contained high ozone and aerosol pollutant concentrations, impacted surface air quality substantially. After some modifications of its physical and chemical parameters, the Meteorological Research Institute Chemistry-Climate Model, version 2 (MRI-CCM2) approximately reproduced the high-ozone volume-mixing ratio. The Model of Aerosol Species IN the Global AtmospheRe (MASINGAR) mk-2 successfully predicted high aerosol concentrations, but the predicted peak aerosol optical thickness was about one-third of the observed value.


2010 ◽  
Vol 10 (16) ◽  
pp. 7763-7773 ◽  
Author(s):  
X. Yang ◽  
J. A. Pyle ◽  
R. A. Cox ◽  
N. Theys ◽  
M. Van Roozendael

Abstract. In the last two decades, significant depletion of boundary layer ozone (ozone depletion events, ODEs) has been observed in both Arctic and Antarctic spring. ODEs are attributed to catalytic destruction by bromine radicals (Br plus BrO), especially during bromine explosion events (BEs), when high concentrations of BrO periodically occur. However, neither the exact source of bromine nor the mechanism for sustaining the observed high BrO concentrations is completely understood. Here, by considering the production of sea salt aerosol from snow lying on sea ice during blowing snow events and the subsequent release of bromine, we successfully simulate the BEs using a global chemistry transport model. We find that heterogeneous reactions play an important role in sustaining a high fraction of the total inorganic bromine as BrO. We also find that emissions of bromine associated with blowing snow contribute significantly to BrO at mid-latitudes. Modeled tropospheric BrO columns generally compare well with the tropospheric BrO columns retrieved from the GOME satellite instrument (Global Ozone Monitoring Experiment). The additional blowing snow bromine source, identified here, reduces modeled high latitude lower tropospheric ozone amounts by up to an average 8% in polar spring.


2016 ◽  
Vol 16 (21) ◽  
pp. 14025-14039 ◽  
Author(s):  
Dimitris Akritidis ◽  
Andrea Pozzer ◽  
Prodromos Zanis ◽  
Evangelos Tyrlis ◽  
Bojan Škerlak ◽  
...  

Abstract. We study the contribution of tropopause folds in the summertime pool of tropospheric ozone over the eastern Mediterranean and the Middle East (EMME) with the aid of the ECHAM5/MESSy Atmospheric Chemistry (EMAC) model. Tropopause fold events in EMAC simulations were identified with a 3-D labeling algorithm that detects folds at grid points where multiple crossings of the dynamical tropopause are computed. Subsequently the events featuring the largest horizontal and vertical extent were selected for further study. For the selection of these events we identified a significant contribution of the stratospheric ozone reservoir to the high concentrations of ozone in the middle and lower free troposphere over the EMME. A distinct increase of ozone is found over the EMME in the middle troposphere during summer as a result of the fold activity, shifting towards the southeast and decreasing altitude. We find that the interannual variability of near-surface ozone over the eastern Mediterranean (EM) during summer is related to that of both tropopause folds and ozone in the free troposphere.


2011 ◽  
Vol 45 (32) ◽  
pp. 5716-5724 ◽  
Author(s):  
Milica Arsić ◽  
Djordje Nikolić ◽  
Predrag Djordjević ◽  
Ivan Mihajlović ◽  
Živan Živković

2014 ◽  
Vol 14 (2) ◽  
pp. 1287-1316 ◽  
Author(s):  
E. von Schneidemesser ◽  
M. Vieno ◽  
P. S. Monks

Abstract. Ground-level ozone is recognized to be a threat to human health (WHO, 2003), have a deleterious impact on vegetation (Fowler et al., 2009), is also an important greenhouse gas (IPCC, 2007) and key to the oxidative ability of the atmosphere (Monks et al., 2009). Owing to its harmful effect on health, much policy and mitigation effort has been put into reducing its precursors – the nitrogen oxides (NOx) and non-methane volatile organic compounds (NMVOCs). The non-linear chemistry of tropospheric ozone formation, dependent mainly on NOx and NMVOC concentrations in the atmosphere, makes controlling tropospheric ozone complex. Furthermore, the concentration of ozone at any given point is a complex superimposition of in-situ produced or destroyed ozone and transported ozone on the regional and hemispheric-scale. In order to effectively address ozone, a more detailed understanding of its origins is needed. Here we show that roughly half (5 μg m−3) of the observed increase in urban (London) ozone (10 μg m−3) in the UK from 1998 to 2008 is owing to factors of local origin, in particular, the change in NO : NO2 ratio, NMVOC : NOx balance, NMVOC speciation, and emission reductions (including NOx titration). In areas with previously higher large concentrations of nitrogen oxides, ozone that was previously suppressed by high concentrations of NO has now been "unmasked", as in London and other urban areas of the UK. The remaining half (approximately 5 μg m−3) of the observed ozone increase is attributed to non-local factors such as long-term transport of ozone, changes in background ozone, and meteorological variability. These results show that a two-pronged approach, local action and regional-to-hemispheric cooperation, is needed to reduce ozone and thereby population exposure, which is especially important for urban ozone.


Sign in / Sign up

Export Citation Format

Share Document