scholarly journals Avoiding high ozone pollution in Delhi, India

2021 ◽  
Author(s):  
Ying Chen ◽  
Gufran Beig ◽  
Scott Archer-Nicholls ◽  
Will Drysdale ◽  
W. Joe F. Acton ◽  
...  
Keyword(s):  
Air Quality ◽  
Surface Ozone ◽  
Light Extinction ◽  
Ozone Pollution ◽  
Ozone Photochemistry

Quantify the influence of aerosol light extinction on surface ozone photochemistry, highlight controlling VOC for improving air quality in Delhi.

scholarly journals Impacts of future land use and land cover change on mid-21<sup>st</sup>-century surface ozone air quality: Distinguishing between the biogeophysical and biogeochemical effects

2019 ◽  
Author(s):  
Lang Wang ◽  
Amos P. K. Tai ◽  
Chi-Yung Tam ◽  
Mehliyar Sadiq ◽  
Peng Wang ◽  
...  
Keyword(s):  
Land Use ◽  
Air Quality ◽  
Land Cover ◽  
Dry Deposition ◽  
Surface Ozone ◽  
Boreal Summer ◽  
Ozone Pollution ◽  
Lulc Change ◽  
Lulc Changes ◽  
The Impact

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.

scholarly journals Vegetation feedbacks during drought exacerbate ozone air pollution extremes in Europe

2020 ◽  
Author(s):  
Meiyun Lin ◽  
Larry Horowitz ◽  
Yuanyu Xie ◽  
Fabien Paulot ◽  
Sergey Malyshev ◽  
...  
Keyword(s):  
Air Pollution ◽  
Air Quality ◽  
Drought Stress ◽  
Dry Deposition ◽  
Surface Ozone ◽  
Ozone Pollution ◽  
Ozone Uptake ◽  
Vegetation Feedbacks ◽  
Ozone Episodes ◽  
Pollution Episodes

&lt;p&gt;This study highlights a previously under-appreciated &amp;#8220;climate penalty&amp;#8221; feedback mechanism - namely, substantial reductions of ozone uptake by water stressed vegetation &amp;#8211; as a missing piece to the puzzle of why European ozone pollution episodes have not decreased as expected in recent decades, despite marked reductions in regional emissions of ozone precursors due to regulatory changes. The most extreme ozone pollution episodes are linked to heatwaves and droughts, which are increasing in frequency and intensity over Europe, with severe impacts on natural and human systems. Under drought stress, plants close their stomata to reduce water loss, consequently limiting the ozone uptake by vegetation (a component of dry deposition), leading to increased surface ozone concentrations. Such land-biosphere feedbacks are often overlooked in prior air quality projections, owing to a lack of process-based model formulations. Here, we use six decades of observations and Earth system model simulations (1960-2018) with an interactive dry deposition scheme to show that declining ozone removal by water-stressed vegetation in the warming climate exacerbate ozone air pollution over Europe. Incorporated into a dynamic vegetation land &amp;#8211; atmospheric chemistry &amp;#8211; climate model, the dry deposition scheme mechanistically describes the response of ozone deposition to atmospheric CO&lt;sub&gt;2&amp;#160;&lt;/sub&gt;concentration, canopy air vapor pressure deficit, and soil water availability. Our observational and modeling analyses reveal drought stress causing as much as 70% reductions in ozone removal by forests. Reduced ozone removal by water-stressed vegetation worsens peak ozone episodes during European mega-droughts, such as the 2003 event, offsetting much of the air quality improvements gained from regional emission controls. Accounting for vegetation feedbacks leads to a three-fold increase in high surface ozone events above 80 ppbv (8-hour average) and a 20% increase in the sensitivity of ozone pollution extremes (95&lt;sup&gt;th&amp;#160;&lt;/sup&gt;percentile) to increasing temperature. As the frequency of hot and dry summers is expected to increase in the coming decades, this ozone climate penalty could be severe and therefore needs to be considered when designing clean air policy in the European Union.&amp;#160;&lt;/p&gt;&lt;p&gt;Notes: This study is currently under review for possible publication in Nature Climate Change.&amp;#160;&lt;/p&gt;

scholarly journals Evaluation of regional simulation of surface ozone over Southeast Asia using ground-based observation at two existing Global Atmospheric Watch stations

2021 ◽  
Vol 880 (1) ◽  
pp. 012006
Author(s):  
Didin Agustian Permadi ◽  
Nguyen Thi Kim Oanh
Keyword(s):  
Air Quality ◽  
Urban Areas ◽  
Emission Inventory ◽  
Surface Ozone ◽  
Wrf Model ◽  
Ambient Air ◽  
Quality Standard ◽  
Ozone Pollution ◽  
Ozone Precursors ◽  
Remote Sites

Abstract High level of ground level ozone concentrations was found in most of Southeast Asian (SEA) large cities and often exceeded the national ambient air quality standard. Ozone and PM10 are among of the critical air quality parameters that cause the unhealthy air quality index. Effort to mitigate ozone pollution is greatly complicated due to the photochemistry processes therefore photochemical smog modelling has been widely used. Surface ozone simulation in SEA was done using CHIMERE and weather research forecast (WRF) model. Emission inventory of ozone precursors was done for three countries in the domain, i.e. Indonesia, Thailand and Cambodia. Modelling performance evaluation for meteorological parameters and ozone at the SEA big cities was done in another study. This paper focused on the model evaluation conducted at the two remote sites represented by 2 (two) global atmospheric watch (GAW) remote stations of Bukit Kototabang (BKT) and Danum Valley (DNV). Evaluation result showed an overestimation of observed ozone in BKT while a contradictive result was seen in DNV station which was due to the ozone chemistry and inaccurate estimation of emissions (both anthropogenic and biogenic emission). The evaluation conducted at the remote sites was not even better than that conducted previously at the urban areas. Statistically, only mean normalized gross error and unpaired peak accuracy values that satisfy the criteria for surface ozone modelling suggesting major improvement required for ozone precursors emission inventory data.

scholarly journals What have we missed when studying the impact of aerosols on surface ozone via changing photolysis rates?

2020 ◽  
Vol 20 (18) ◽  
pp. 10831-10844 ◽  
Author(s):  
Jinhui Gao ◽  
Ying Li ◽  
Bin Zhu ◽  
Bo Hu ◽  
Lili Wang ◽  
...  
Keyword(s):  
Source Apportionment ◽  
Surface Ozone ◽  
Vertical Direction ◽  
Light Extinction ◽  
Chemical Production ◽  
Long Distance ◽  
Source Regions ◽  
Photolysis Rate ◽  
Ozone Photochemistry ◽  
The Impact

Abstract. Previous studies have emphasized that the decrease in photolysis rate at the surface induced by the light extinction of aerosols could weaken ozone photochemistry and then reduce surface ozone. However, quantitative studies have shown that weakened photochemistry leads to a much greater reduction in the net chemical production of ozone, which does not match the reduction in surface ozone. This suggests that in addition to photochemistry, some other physical processes related to the variation of ozone should also be considered. In this study, the Weather Research and Forecasting with Chemistry (WRF-Chem) model coupled with the ozone source apportionment method was applied to determine the mechanism of ozone reduction induced by aerosols over central East China (CEC). Our results showed that weakened ozone photochemistry led to a significant reduction in ozone net chemical production, which occurred not only at the surface but also within the lowest several hundred meters in the planetary boundary layer (PBL). Meanwhile, a larger ozone gradient was formed in the vertical direction, which led to the high concentrations of ozone aloft being entrained by turbulence from the top of the PBL to the surface and partly counteracting the reduction in surface ozone. In addition, contribution from dry deposition was weakened due to the decrease in surface ozone concentration. The reduction in the ozone's sink also slowed down the rate of the decrease in surface ozone. Ozone in the upper layer of the PBL was also reduced, which was induced by much ozone aloft being entrained downward. Therefore, by affecting the photolysis rate, the impact of aerosols was a reduction in ozone not only at the surface but also throughout the entire PBL during the daytime over CEC in this study. The ozone source apportionment results showed that 41.4 %–66.3 % of the reduction in surface ozone came from local and adjacent source regions, which suggested that the impact of aerosols on ozone from local and adjacent regions was more significant than that from long-distance regions. The results also suggested that while controlling the concentration of aerosols, simultaneously controlling ozone precursors from local and adjacent source regions is an effective way to suppress the increase in surface ozone over CEC at present.

scholarly journals The influence of European pollution on ozone in the Near East and northern Africa

2008 ◽  
Vol 8 (1) ◽  
pp. 1913-1950 ◽  
Author(s):  
B. N. Duncan ◽  
J. J. West ◽  
Y. Yoshida ◽  
A. M. Fiore ◽  
J. R. Ziemke
Keyword(s):  
Boundary Layer ◽  
Air Quality ◽  
Near East ◽  
Surface Ozone ◽  
Northern Africa ◽  
Ozone Production ◽  
Ozone Pollution ◽  
East European ◽  
European Health ◽  
Ozone Precursor

Abstract. We present a modeling study of the long-range transport of pollution from Europe, showing that European emissions regularly elevate surface ozone by as much as 20 ppbv in summer in northern Africa and the Near East. European emissions cause 50–150 additional violations per year (i.e., above those that would occur without European pollution) of the European health standard for ozone (8-h average >120 μg/m3 or ~60 ppbv) in northern Africa and the Near East. We estimate that 19 000 additional mortalities occur annually in these regions from exposure to European ozone pollution and 50 000 additional deaths globally; the majority of the additional deaths occurs outside of Europe. Much of the pollution from Europe is exported southward at low altitudes in summer to the Mediterranean Sea, northern Africa and the Near East, regions with favorable photochemical environments for ozone production. Our results suggest that assessments of the human health benefits of reducing ozone precursor emissions in Europe should include effects outside of Europe, and that comprehensive planning to improve air quality in northern Africa and the Near East likely needs to address European emissions. We also show that the tropospheric ozone column data product derived from the OMI and MLS instruments is currently of limited value for air quality applications as the portion of the column above the boundary layer and below the tropopause is large and variable, effectively obscuring the boundary layer signal.

scholarly journals Skill in forecasting extreme ozone pollution episodes with a global atmospheric chemistry model

2014 ◽  
Vol 14 (15) ◽  
pp. 7721-7739 ◽  
Author(s):  
J. L. Schnell ◽  
C. D. Holmes ◽  
A. Jangam ◽  
M. J. Prather
Keyword(s):  
Air Quality ◽  
Atmospheric Chemistry ◽  
Climate Models ◽  
Transport Model ◽  
Surface Ozone ◽  
The United States ◽  
Ozone Pollution ◽  
Mapping Algorithm ◽  
The Individual ◽  
Pollution Episodes

Abstract. From the ensemble of stations that monitor surface air quality over the United States and Europe, we identify extreme ozone pollution events and find that they occur predominantly in clustered, multiday episodes with spatial extents of more than 1000 km. Such scales are amenable to forecasting with current global atmospheric chemistry models. We develop an objective mapping algorithm that uses the heterogeneous observations of the individual surface sites to calculate surface ozone averaged over 1° by 1° grid cells, matching the resolution of a global model. Air quality extreme (AQX) events are identified locally as statistical extremes of the ozone climatology and not as air quality exceedances. With the University of California, Irvine chemistry-transport model (UCI CTM) we find there is skill in hindcasting these extreme episodes, and thus identify a new diagnostic using global chemistry–climate models (CCMs) to identify changes in the characteristics of extreme pollution episodes in a warming climate.

scholarly journals What have we missed when studying the impact of aerosols on surface ozone via changing photolysis rates?

2020 ◽  
Author(s):  
Jinhui Gao ◽  
Ying Li ◽  
Bin Zhu ◽  
Bo Hu ◽  
Lili Wang ◽  
...  
Keyword(s):  
Source Apportionment ◽  
Surface Ozone ◽  
Vertical Direction ◽  
Light Extinction ◽  
Chemical Production ◽  
Long Distance ◽  
Source Regions ◽  
Photolysis Rate ◽  
Ozone Photochemistry ◽  
The Impact

Abstract. Previous studies have emphasized that the decrease in photolysis rate at the surface induced by the light extinction of aerosols could weaken ozone photochemistry and then reduce surface ozone. However, quantitative studies have shown that weakened photochemistry leads to a much greater reduction in the net chemical production of ozone, which does not match the reduction in surface ozone. This suggested that in addition to photochemistry, some other physical processes related to the variation of ozone should also be considered. In this study, the Weather Research and Forecasting with Chemistry (WRF-Chem) model coupled with the ozone source apportionment method was applied to determine the mechanism of ozone reduction induced by aerosols over Central East China (CEC). Our results showed that weakened ozone photochemistry led to a significant reduction in ozone net chemical production, which occurred not only at the surface but also within the lowest several hundred meters in the planetary boundary layer (PBL). Meanwhile, a larger ozone gradient was formed in vertical direction, which led to the high concentrations of ozone aloft being entrained by turbulence from the top of the PBL to the surface and partly counteracting the reduction in surface ozone. In addition, ozone in the upper layer of the PBL was also reduced, which was also induced by much ozone aloft being entrained downward. Therefore, by affecting the photolysis rate, the impact of aerosols was a reduction in ozone not only at the surface but also throughout the entire PBL during the daytime over the CEC in this study. The ozone source apportionment results showed that 41.4 %–66.3 % of the reduction in surface ozone came from local and adjacent source regions, which suggested that the impact of aerosols on ozone from local and adjacent regions was more significant than that from long-distance regions. The results also suggested that while controlling the concentration of aerosols, simultaneously controlling ozone precursors from local and adjacent source regions is an effective way to suppress the increase in surface ozone over CEC at present.

scholarly journals Skill in forecasting extreme ozone pollution episodes with a global atmospheric chemistry model

2014 ◽  
Vol 14 (5) ◽  
pp. 6261-6310 ◽  
Author(s):  
J. L. Schnell ◽  
C. D. Holmes ◽  
A. Jangam ◽  
M. J. Prather
Keyword(s):  
Air Quality ◽  
Atmospheric Chemistry ◽  
Climate Models ◽  
Transport Model ◽  
Surface Ozone ◽  
The United States ◽  
Ozone Pollution ◽  
Mapping Algorithm ◽  
The Individual ◽  
Pollution Episodes

Abstract. From the ensemble of stations that monitor surface air quality over the United States and Europe, we identify extreme ozone pollution events and find that they occur predominantly in clustered, multi-day episodes with spatial extents of more than 1000 km. Such scales are amenable to forecasting with current global atmospheric chemistry models. We develop an objective mapping algorithm that uses the heterogeneous observations of the individual surface sites to calculate surface ozone averaged over 1° by 1° grid cells, matching the resolution of a global model. Air quality extreme (AQX) events are identified locally as statistical extremes of the ozone climatology and not as air quality exceedances. With the University of California, Irvine chemistry-transport model (CTM) we find there is skill in hindcasting these extreme episodes, and thus identify a new diagnostic using global chemistry-climate models (CCM) to identify changes in the characteristics of extreme pollution episodes in a warming climate.

scholarly journals The long-term trend and production sensitivity change in the US ozone pollution from observations and model simulations

2020 ◽  
Vol 20 (5) ◽  
pp. 3191-3208 ◽  
Author(s):  
Hao He ◽  
Xin-Zhong Liang ◽  
Chao Sun ◽  
Zhining Tao ◽  
Daniel Q. Tong
Keyword(s):  
United States ◽  
Air Quality ◽  
Surface Ozone ◽  
The United States ◽  
Early Morning ◽  
Ozone Pollution ◽  
Late Afternoon ◽  
The Past ◽  
The Us

Abstract. We investigated the ozone pollution trend and its sensitivity to key precursors from 1990 to 2015 in the United States using long-term EPA Air Quality System (AQS) observations and mesoscale simulations. The modeling system, a coupled regional climate–air quality model (CWRF-CMAQ; Climate-Weather Research Forecast and the Community Multiscale Air Quality), captured well the summer surface ozone pollution during the past decades, having a mean slope of linear regression with AQS observations of ∼0.75. While the AQS network has limited spatial coverage and measures only a few key chemical species, CWRF-CMAQ provides comprehensive simulations to enable a more rigorous study of the change in ozone pollution and chemical sensitivity. Analysis of seasonal variations and diurnal cycle of ozone observations showed that peak ozone concentrations in the summer afternoon decreased ubiquitously across the United States, up to 0.5 ppbv yr−1 in major non-attainment areas such as Los Angeles, while concentrations at certain hours such as the early morning and late afternoon increased slightly. Consistent with the AQS observations, CMAQ simulated a similar decreasing trend of peak ozone concentrations in the afternoon, up to 0.4 ppbv yr−1, and increasing ozone trends in the early morning and late afternoon. A monotonically decreasing trend (up to 0.5 ppbv yr−1) in the odd oxygen (Ox=O3+NO2) concentrations are simulated by CMAQ at all daytime hours. This result suggests that the increased ozone in the early morning and late afternoon was likely caused by reduced NO–O3 titration, driven by continuous anthropogenic NOx emission reductions in the past decades. Furthermore, the CMAQ simulations revealed a shift in chemical regimes of ozone photochemical production. From 1990 to 2015, surface ozone production in some metropolitan areas, such as Baltimore, has transited from a VOC-sensitive environment (>50 % probability) to a NOx-sensitive regime. Our results demonstrated that the long-term CWRF-CMAQ simulations can provide detailed information of the ozone chemistry evolution under a changing climate and may partially explain the US ozone pollution responses to regional and national regulations.

scholarly journals Comment on “Simulation of Surface Ozone Pollution in the Central Gulf Coast Region Using WRF/Chem Model: Sensitivity to PBL and Land Surface Physics”

2011 ◽  
Vol 2011 ◽  
pp. 1-3 ◽  
Author(s):  
Jonathan E. Pleim
Keyword(s):  
Boundary Layer ◽  
Air Quality ◽  
Land Surface ◽  
Gulf Coast ◽  
Surface Ozone ◽  
Air Quality Modeling ◽  
Weather Research And Forecasting ◽  
Ozone Pollution ◽  
Quality Modeling ◽  
Gulf Coast Region

A recently published meteorology and air quality modeling study has several serious deficiencies deserving comment. The study uses the weather research and forecasting/chemistry (WRF/Chem) model to compare and evaluate boundary layer and land surface modeling options. The most serious of the study's deficiencies is reporting WRF/Chem results for both meteorological and chemical quantities using the asymmetric convective model version 2 (ACM2). While the ACM2 is a valid model option for WRF, it has not yet been implemented for the chemical portion of the WRF/Chem model. Hence, the reported air quality modeling results using ACM2 are invalid. Furthermore, publication of these results gives the erroneous impression that the ACM2 model is not well suited for air quality applications when, in fact, it is the default boundary layer model in the community multiscale air quality (CMAQ) model.

Sign in / Sign up

Export Citation Format

Share Document