scholarly journals Regional Differences of Primary Meteorological Factors Impacting O3 Variability in South Korea

Atmosphere ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 74 ◽  
Author(s):  
Yeomin Jeong ◽  
Hwa Woon Lee ◽  
Wonbae Jeon

Surface ozone (O3) is a harmful pollutant and effective strategies must be developed for its reduction. In this study, the impact of meteorological factors on the annual O3 variability for South Korea were analyzed. In addition, the regional differences of meteorological factors in six air quality regions in South Korea (Seoul Metropolitan Area, SMA; Central region, CN; Honam, HN; Yeongnam, YN; Gangwon, GW; Jeju, JJ) were compared. The analysis of ground observation data from 2001 to 2017 revealed that the long-term variability of O3 concentration in South Korea continuously increased since 2001, and the upward trend in 2010 to 2017 (Period 2, PRD2) was 29.8% higher than that in 2001 to 2009 (Period 1, PRD1). This was because the meteorological conditions during PRD2 became relatively favorable for high O3 concentrations compared to conditions during PRD1. In particular, the increase in the solar radiation (SR) and maximum temperature (TMAX) and the decrease in the precipitation (PRCP) and wind speed (WS) of South Korea in PRD2 were identified as the main causes for the rise in O3 concentrations. When meteorological factors and O3 variability were compared among the six air quality regions in South Korea during PRD1 and PRD2, significant differences were observed. This indicated that different meteorological changes occurred in South Korea after 2010 due to the different topographical characteristics of each region; thus, O3 variability also changed differently in each region. Interestingly, for the regions with almost similar meteorological changes after 2010, the O3 concentration changed differently depending on the difference in the distribution of emissions. These results indicate that the O3–meteorology relationship shows spatiotemporal differences depending on the topographical and emission distribution characteristics of each area and implies that it is necessary to fully consider such differences for efficient O3 reduction.

2013 ◽  
Vol 13 (24) ◽  
pp. 12215-12231 ◽  
Author(s):  
Z. S. Stock ◽  
M. R. Russo ◽  
T. M. Butler ◽  
A. T. Archibald ◽  
M. G. Lawrence ◽  
...  

Abstract. We examine the effects of ozone precursor emissions from megacities on present-day air quality using the global chemistry–climate model UM-UKCA (UK Met Office Unified Model coupled to the UK Chemistry and Aerosols model). The sensitivity of megacity and regional ozone to local emissions, both from within the megacity and from surrounding regions, is important for determining air quality across many scales, which in turn is key for reducing human exposure to high levels of pollutants. We use two methods, perturbation and tagging, to quantify the impact of megacity emissions on global ozone. We also completely redistribute the anthropogenic emissions from megacities, to compare changes in local air quality going from centralised, densely populated megacities to decentralised, lower density urban areas. Focus is placed not only on how changes to megacity emissions affect regional and global NOx and O3, but also on changes to NOy deposition and to local chemical environments which are perturbed by the emission changes. The perturbation and tagging methods show broadly similar megacity impacts on total ozone, with the perturbation method underestimating the contribution partially because it perturbs the background chemical environment. The total redistribution of megacity emissions locally shifts the chemical environment towards more NOx-limited conditions in the megacities, which is more conducive to ozone production, and monthly mean surface ozone is found to increase up to 30% in megacities, depending on latitude and season. However, the displacement of emissions has little effect on the global annual ozone burden (0.12% change). Globally, megacity emissions are shown to contribute ~3% of total NOy deposition. The changes in O3, NOx and NOy deposition described here are useful for quantifying megacity impacts and for understanding the sensitivity of megacity regions to local emissions. The small global effects of the 100% redistribution carried out in this study suggest that the distribution of emissions on the local scale is unlikely to have large implications for chemistry–climate processes on the global scale.


2020 ◽  
Vol 237 ◽  
pp. 03012
Author(s):  
Christoph Senff ◽  
Andrew Langford ◽  
Raul Alvarez ◽  
Tim Bonin ◽  
Alan Brewer ◽  
...  

Recently, two air quality campaigns were conducted in the southwestern United States to study the impact of transported ozone, stratospheric intrusions, and fire emissions on ground-level ozone concentrations. The California Baseline Ozone Transport Study (CABOTS) took place in May – August 2016 covering the central California coast and San Joaquin Valley, and the Fires, Asian, and Stratospheric Transport Las Vegas Ozone Study (FAST-LVOS) was conducted in the greater Las Vegas, Nevada area in May – June 2017. During these studies, nearly 1000 hours of ozone and aerosol profile data were collected with the NOAA TOPAZ lidar. A Doppler wind lidar and a radar wind profiler provided continuous observations of atmospheric turbulence, horizontal winds, and mixed layer height. These measurements allowed us to directly observe the degree to which ozone transport layers aloft were entrained into the boundary layer and to quantify the resulting impact on surface ozone levels. Mixed layer heights in the San Joaquin Valley during CABOTS were generally below 1 km above ground level (AGL), while boundary layer heights in Las Vegas during FAST-LVOS routinely exceeded 3 km AGL and occasionally reached up to 4.5 km AGL. Consequently, boundary layer entrainment was more often observed during FAST-LVOS, while most elevated ozone layers passed untapped over the San Joaquin Valley during CABOTS.


2019 ◽  
Author(s):  
Lang Wang ◽  
Amos P. K. Tai ◽  
Chi-Yung Tam ◽  
Mehliyar Sadiq ◽  
Peng Wang ◽  
...  

Abstract. Surface ozone (O3) is an important air pollutant and greenhouse gas. Land use and land cover (LULC) is one of the critical factors influencing ozone, in addition to anthropogenic emissions and climate. LULC change can on the one hand affect ozone biogeochemically, i.e., via dry deposition and biogenic emissions of volatile organic compounds (VOCs). LULC change can on the other hand alter regional- to large-scale climate through modifying albedo and evapotranspiration, which can lead to changes in surface temperature, hydrometeorology and atmospheric circulation that can ultimately impact ozone biogeophysically over local and remote areas. Such biogeophysical effects of LULC on ozone are largely understudied. This study investigates the individual and combined biogeophysical and biogeochemical effects of LULC on ozone, and explicitly examines the critical pathway for how LULC change impacts ozone pollution. A global coupled atmosphere–chemistry–land model is driven by projected LULC changes from the present day (2000) to future (2050) under RCP4.5 and RCP8.5 scenarios, focusing on the boreal summer. Results reveal that when considering biogeochemical effects only, surface ozone is predicted to have slight changes by up to 2 ppbv maximum in some areas due to LULC changes. It is primarily driven by changes in isoprene emission and dry deposition counteracting each other in shaping ozone. In contrast, when considering the integrated effect of LULC, ozone is more substantially altered by up to 6 ppbv over several regions, reflecting the importance of biogeophysical effects on ozone changes. Furthermore, large areas of these ozone changes are found over the regions without LULC changes where the biogeophysical effect is the only pathway for such changes. The mechanism is likely that LULC change induces a regional circulation response, in particular the formation of anomalous stationary high-pressure systems, shifting of moisture transport, and near-surface warming over the middle-to-high northern latitudes in boreal summer, owing to associated changes in albedo and surface energy budget. Such temperature changes then alter ozone substantially. We conclude that the biogeophysical effect of LULC is an important pathway for the influence of LULC change on ozone air quality over both local and remote regions, even in locations without significant LULC changes. Overlooking the impact of biogeophysical effect may cause evident underestimation of the impacts of LULC change on ozone pollution.


2021 ◽  
Author(s):  
Claire Lamotte ◽  
Jonathan Guth ◽  
Virginie Marécal ◽  
Giuseppe Salerno ◽  
Nicolas Theys ◽  
...  

<p><span>Volcanic eruptions are events that can eject several tons of material into the atmosphere. Among these emissions, sulfur dioxide is the main sulfurous volcanic gas. It can form sulfate aerosols that are harmful to health or, being highly soluble, it can condense in water particles and form acid rain. Thus, volcanic eruptions can have an environmental impact on a regional scale.</span></p><p><span>The Mediterranean region is very interesting from this point of view because it is a densely populated region with a strong anthropogenic activity, therefore polluted, in which Mount Etna is also located. Mount Etna is the largest passive SO<sub>2</sub> emitter in Europe, but it can also sporadically produce strong eruptive events. It is then likely that the additional input of sulfur compounds into the atmosphere by volcanic emissions may have effects on the regional atmospheric sulfur composition.</span></p><p><span>We are particularly investigating the eruption of Mount Etna on December 24, 2018 [Corradini et al, 2020]. This eruption took place along a 2 km long breach on the side of the volcano, thus at a lower altitude than its main crater. About 100 kt of SO<sub>2</sub> and 35 kt of ash were released in total, between December 24 and 30. With the exception of the 24th, the quantities of ash were always lower than the SO<sub>2.</sub></span></p><p><span>The availability of the TROPOMI SO<sub>2</sub><sub></sub></span><span>column </span><span>estimates, at fine </span><span>spatial</span><span> resolution </span><span>(7 km x 3.5 km at nadir) and </span><span>associated averaging kernels</span><span>,</span><span> during this eruptive period made it also an excellent case study. </span><span>It </span><span>allow</span><span>s</span><span> us to follow the evolution of SO<sub>2</sub> in the volcanic plume over several days.</span></p><p><span>Using the CNRM MOCAGE chemistry-transport model (CTM), we aim to quantify the impact of this volcanic eruption on atmospheric composition, sulfur deposition and air quality at the regional scale. The comparison of the model with the TROPOMI observation data allows us to assess the ability of the model to properly represent the plume. In spite of a particular meteorological situation, leading to a complex plume transport, MOCAGE shows a good agreement with TROPOMI observations. Thus, from the MOCAGE simulation, we can evaluate the impact of the eruption on the regional concentrations of SO<sub>2</sub> and sulfate aerosols, but also analyse the quantities of dry and wet deposition, and compare it to surface measurement stations.</span></p>


Author(s):  
Qinling Yan ◽  
Sanyi Tang ◽  
Zhen Jin ◽  
Yanni Xiao

Five epidemic waves of A(H7N9) occurred between March 2013 and May 2017 in China. However, the potential risk factors associated with disease transmission remain unclear. To address the spatial–temporal distribution of the reported A(H7N9) human cases (hereafter referred to as “cases”), statistical description and geographic information systems were employed. Based on long-term observation data, we found that males predominated the majority of A(H7N9)-infected individuals and that most males were middle-aged or elderly. Further, wavelet analysis was used to detect the variation in time-frequency between A(H7N9) cases and meteorological factors. Moreover, we formulated a Poisson regression model to explore the relationship among A(H7N9) cases and meteorological factors, the number of live poultry markets (LPMs), population density and media coverage. The main results revealed that the impact factors of A(H7N9) prevalence are manifold, and the number of LPMs has a significantly positive effect on reported A(H7N9) cases, while the effect of weekly average temperature is significantly negative. This confirms that the interaction of multiple factors could result in a serious A(H7N9) outbreak. Therefore, public health departments adopting the corresponding management measures based on both the number of LPMs and the forecast of meteorological conditions are crucial for mitigating A(H7N9) prevalence.


2009 ◽  
Vol 9 (12) ◽  
pp. 4115-4129 ◽  
Author(s):  
N. Unger ◽  
S. Menon ◽  
D. M. Koch ◽  
D. T. Shindell

Abstract. The development of effective emissions control policies that are beneficial to both climate and air quality requires a detailed understanding of all the feedbacks in the atmospheric composition and climate system. We perform sensitivity studies with a global atmospheric composition-climate model to assess the impact of aerosols on tropospheric chemistry through their modification on clouds, aerosol-cloud interactions (ACI). The model includes coupling between both tropospheric gas-phase and aerosol chemistry and aerosols and liquid-phase clouds. We investigate past impacts from preindustrial (PI) to present day (PD) and future impacts from PD to 2050 (for the moderate IPCC A1B scenario) that embrace a wide spectrum of precursor emission changes and consequential ACI. The aerosol indirect effect (AIE) is estimated to be −2.0 Wm−2 for PD-PI and −0.6 Wm−2 for 2050-PD, at the high end of current estimates. Inclusion of ACI substantially impacts changes in global mean methane lifetime across both time periods, enhancing the past and future increases by 10% and 30%, respectively. In regions where pollution emissions increase, inclusion of ACI leads to 20% enhancements in in-cloud sulfate production and ~10% enhancements in sulfate wet deposition that is displaced away from the immediate source regions. The enhanced in-cloud sulfate formation leads to larger increases in surface sulfate across polluted regions (~10–30%). Nitric acid wet deposition is dampened by 15–20% across the industrialized regions due to ACI allowing additional re-release of reactive nitrogen that contributes to 1–2 ppbv increases in surface ozone in outflow regions. Our model findings indicate that ACI must be considered in studies of methane trends and projections of future changes to particulate matter air quality.


2020 ◽  
Vol 20 (10) ◽  
pp. 6015-6036
Author(s):  
Soyoung Ha ◽  
Zhiquan Liu ◽  
Wei Sun ◽  
Yonghee Lee ◽  
Limseok Chang

Abstract. The Korean Geostationary Ocean Color Imager (GOCI) satellite has monitored the East Asian region in high temporal (e.g., hourly) and spatial resolution (e.g., 6 km) every day for the last decade, providing unprecedented information on air pollutants over the upstream region of the Korean Peninsula. In this study, the GOCI aerosol optical depth (AOD), retrieved at the 550 nm wavelength, is assimilated to enhance the quality of the aerosol analysis, thereby making systematic improvements to air quality forecasting over South Korea. For successful data assimilation, GOCI retrievals are carefully investigated and processed based on data characteristics such as temporal and spatial distribution. The preprocessed data are then assimilated in the three-dimensional variational data assimilation (3D-Var) technique for the Weather Research and Forecasting model coupled with Chemistry (WRF-Chem). For the Korea–United States Air Quality (KORUS-AQ) period (May 2016), the impact of GOCI AOD on the accuracy of surface PM2.5 prediction is examined by comparing with effects of other observations including Moderate Resolution Imaging Spectroradiometer (MODIS) sensors and surface PM2.5 observations. Consistent with previous studies, the assimilation of surface PM2.5 measurements alone still underestimates surface PM2.5 concentrations in the following forecasts, and the forecast improvements last only for about 6 h. When GOCI AOD retrievals are assimilated with surface PM2.5 observations, however, the negative bias is diminished and forecast skills are improved up to 24 h, with the most significant contributions to the prediction of heavy pollution events over South Korea.


2017 ◽  
Vol 17 (17) ◽  
pp. 10315-10332 ◽  
Author(s):  
Hyun Cheol Kim ◽  
Eunhye Kim ◽  
Changhan Bae ◽  
Jeong Hoon Cho ◽  
Byeong-Uk Kim ◽  
...  

Abstract. The impact of regional emissions (e.g., domestic and international) on surface particulate matter (PM) concentrations in the Seoul metropolitan area (SMA), South Korea, and its sensitivities to meteorology and emissions inventories are quantitatively estimated for 2014 using regional air quality modeling systems. Located on the downwind side of strong sources of anthropogenic emissions, South Korea bears the full impact of the regional transport of pollutants and their precursors. However, the impact of foreign emissions sources has not yet been fully documented. We utilized two regional air quality simulation systems: (1) a Weather Research and Forecasting and Community Multi-Scale Air Quality (CMAQ) system and (2) a United Kingdom Met Office Unified Model and CMAQ system. The following combinations of emissions inventories are used: the Intercontinental Chemical Transport Experiment-Phase B, the Inter-comparison Study for Asia 2010, and the National Institute of Environment Research Clean Air Policy Support System. Partial contributions of domestic and foreign emissions are estimated using a brute force approach, adjusting South Korean emissions to 50 %. Results show that foreign emissions contributed  ∼  60 % of SMA surface PM concentration in 2014. Estimated contributions display clear seasonal variation, with foreign emissions having a higher impact during the cold season (fall to spring), reaching  ∼  70 % in March, and making lower contributions in the summer,  ∼  45 % in September. We also found that simulated surface PM concentration is sensitive to meteorology, but estimated contributions are mostly consistent. Regional contributions are also found to be sensitive to the choice of emissions inventories.


2020 ◽  
Author(s):  
Soyoung Ha ◽  
Zhiquan Liu

<p>The Korean Geostationary Ocean Color Imager (GOCI) satellite has monitored the East Asian region in high temporal and spatial resolution every day for the last decade, providing unprecedented information on air pollutants over the upstream region of the Korean peninsula. In this study, the GOCI Aerosol optical depth (AOD), retrieved at 550 nm wavelength, is assimilated to ameliorate the analysis quality, thereby making systematic improvements on air quality forecasting in South Korea. For successful data assimilation, GOCI retrievals are carefully investigated and processed based on data characteristics. The preprocessed data are then assimilated in the three-dimensional variational data assimilation (3DVAR) technique for the Weather Research and Forecasting model coupled with Chemistry (WRF-Chem). Over the Korea-United States Air Quality (KORUS-AQ) period (May 2016), the impact of GOCI AOD on the accuracy of air quality forecasting is examined by comparing with other observations including Moderate Resolution Imaging Spectroradiometer (MODIS) sensors and fine particulate matter (PM2.5) observations at the surface. Consistent with previous studies, the assimilation of surface PM2.5 concentrations alone systematically underestimates surface PM2.5 and its positive impact lasts mainly for about 6 h. When GOCI AOD retrievals are assimilated with surface PM2.5 observations, however, the negative bias is diminished and forecasts are improved up to 24 h, with the most significant contributions to the prediction of heavy pollution events over South Korea. The talk will be finished with an introduction of our ongoing efforts on developing the assimilation capability for more sophisticated aerosol schemes such as Model for Simulating Aerosol Interactions and Chemistry (MOSAIC) and the Modal Aerosol Dynamics Model for Europe (MADE)-Volatility basis set (VBS).</p>


2011 ◽  
Vol 11 (6) ◽  
pp. 17699-17757 ◽  
Author(s):  
D. J. Allen ◽  
K. E. Pickering ◽  
R. W. Pinder ◽  
B. H. Henderson ◽  
K. W. Appel ◽  
...  

Abstract. A lightning-nitrogen oxide (NO) algorithm is developed for the regional Community Multiscale Air Quality Model (CMAQ) and used to evaluate the impact of lightning-NO emissions (LNOx) on tropospheric photochemistry over the Eastern United States during the summer of 2006. The scheme assumes flash rates are proportional to the model convective precipitation rate but then adjusts the flash rates locally to match monthly average observations. Over the Eastern United States, LNOx is responsible for 20–25 % of the tropospheric nitrogen dioxide (NO2) column. This additional NO2 reduces the low-bias of simulated NO2 columns with respect to satellite-retrieved Dutch Ozone Monitoring Instrument NO2 (DOMINO) columns from 41 to 14 %. It also adds 10–20 ppbv to upper tropospheric ozone and 1.5–4.5 ppbv to 8-h maximum surface layer ozone, although, on average, the contribution of LNOx to surface ozone is 1–2 ppbv less on poor air quality days. Biases between modeled and satellite-retrieved tropospheric NO2 columns vary greatly between urban and rural locations. In general, CMAQ overestimates columns at urban locations and underestimates columns at rural locations. These biases are consistent with in situ measurements that also indicate that CMAQ has too much NO2 in urban regions and not enough in rural regions. However, closer analysis suggests that most of the differences between modeled and satellite-retrieved urban to rural ratios are likely a consequence of the horizontal and vertical smoothing inherent in columns retrieved by the Ozone Monitoring Instrument (OMI). Within CMAQ, LNOx increases wet deposition of nitrate by 50 % and total deposition of nitrogen by 11 %. This additional deposition reduces the magnitude of the CMAQ low-bias in nitrate wet deposition with respect to National Atmospheric Deposition monitors to near zero. In order to obtain an upper bound on the contribution of uncertainties in chemistry to upper tropospheric NOx low biases, sensitivity calculations with updated chemistry were run for the time period of the Intercontinental Chemical Transport Experiment (INTEX-A) field campaign (summer 2004). After adjusting for possible interferences in NO2 measurements and averaging over the entire campaign, these updates reduced 7–9 km biases from 32 to 17 % and 9–12 km biases from 57 to 46 %. While these changes lead to better agreement, a considerable NO2 low-bias remains in the uppermost troposphere.


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