scholarly journals Evaluation of nitrogen oxides sources and sinks and ozone production in Colombia and surrounding areas

2019 ◽  
Author(s):  
Johannes G. M. Barten ◽  
Laurens N. Ganzeveld ◽  
Auke J. Visser ◽  
Rodrigo Jiménez ◽  
Maarten C. Krol

Abstract. In Colombia, industrialization and a shift towards intensified agriculture have led to increased emissions of air pollutants. However, the baseline state of air quality in Colombia is relatively unknown. In this study we aim to assess the baseline state of air quality in Colombia with a focus on the spatial and temporal variability in emissions and atmospheric burden of nitrogen oxides (NOx = NO + NO2) and evaluate surface NOx, ozone (O3) and carbon monoxide (CO) mixing ratios. We quantify the magnitude and spatial distribution of the four major NOx sources (lightning, anthropogenic activities, soil biogenic emissions and biomass burning), by integrating global NOx emission inventories into the mesoscale meteorology and atmospheric chemistry model WRF-Chem. The comparison with in situ measurements is bound to urban areas whereas the use of remote sensing data allows to also evaluate air quality in remote regions. WRF-Chem was set up for a domain centered over Colombia with a similar resolution as OMI observed NO2 vertical columns as well as the EDGAR anthropogenic emission inventory, both providing information on a ~20 km resolution. However, this apparently poses a challenge regarding comparison with these urban observations. Air mass factors were recalculated based on the vertical distribution of NO2 within WRF-Chem, with respect to the coarse (1° x 1°) a priori profiles. The main reason for recalculation is a more consistent satellite-model comparison but it also reduced the mean bias. WRF-Chem was, on average, able to provide good estimates for tropospheric NO2 columns with an averaged difference of 0.02 x 1015 molecules cm-2, which is

2020 ◽  
Vol 20 (15) ◽  
pp. 9441-9458
Author(s):  
Johannes G. M. Barten ◽  
Laurens N. Ganzeveld ◽  
Auke J. Visser ◽  
Rodrigo Jiménez ◽  
Maarten C. Krol

Abstract. In Colombia, industrialization and a shift towards intensified agriculture have led to increased emissions of air pollutants. However, the baseline state of air quality in Colombia is relatively unknown. In this study we aim to assess the baseline state of air quality in Colombia with a focus on the spatial and temporal variability in emissions and atmospheric burden of nitrogen oxides (NOx = NO + NO2) and evaluate surface NOx, ozone (O3) and carbon monoxide (CO) mixing ratios. We quantify the magnitude and spatial distribution of the four major NOx sources (lightning, anthropogenic activities, soil biogenic emissions and biomass burning) by integrating global NOx emission inventories into the mesoscale meteorology and atmospheric chemistry model, namely Weather Research and Forecasting (WRF) coupled with Chemistry (collectively WRF-Chem), at a similar resolution (∼25 km) to the Emission Database for Global Atmospheric Research (EDGAR) anthropogenic emission inventory and the Ozone Monitoring Instrument (OMI) remote sensing observations. The model indicates the largest contribution by lightning emissions (1258 Gg N yr−1), even after already significantly reducing the emissions, followed by anthropogenic (933 Gg N yr−1), soil biogenic (187 Gg N yr−1) and biomass burning emissions (104 Gg N yr−1). The comparison with OMI remote sensing observations indicated a mean bias of tropospheric NO2 columns over the whole domain (WRF-Chem minus OMI) of 0.02 (90 % CI: [−0.43, 0.70]) ×1015 molecules cm−2, which is <5 % of the mean column. However, the simulated NO2 columns are overestimated and underestimated in regions where lightning and biomass burning emissions dominate, respectively. WRF-Chem was unable to capture NOx and CO urban pollutant mixing ratios, neither in timing nor in magnitude. Yet, WRF-Chem was able to simulate the urban diurnal cycle of O3 satisfactorily but with a systematic overestimation of 10 parts per billion (ppb) due to the equally large underestimation of NO mixing ratios and, consequently, titration. This indicates that these city environments are in the NOx-saturated regime with frequent O3 titration. We conducted sensitivity experiments with an online meteorology–chemistry single-column model (SCM) to evaluate how WRF-Chem subgrid-scale-enhanced emissions could explain an improved representation of the observed O3, CO and NOx diurnal cycles. Interestingly, the SCM simulation, showing especially a shallower nocturnal inversion layer, results in a better representation of the observed diurnal cycle of urban pollutant mixing ratios without an enhancement in emissions. This stresses that, besides application of higher-resolution emission inventories and model experiments, the diurnal cycle in boundary layer dynamics (and advection) should be critically evaluated in models such as WRF-Chem to assess urban air quality. Overall, we present a concise method to quantify air quality in regions with limited surface measurements by integrating in situ and remote sensing observations. This study identifies four distinctly different source regions and shows their interannual and seasonal variability during the last 1.5 decades. It serves as a base to assess scenarios of future air quality in Colombia or similar regions with contrasting emission regimes, complex terrain and a limited air quality monitoring network.


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.


2016 ◽  
Vol 189 ◽  
pp. 407-437 ◽  
Author(s):  
Christian Ehlers ◽  
Dieter Klemp ◽  
Franz Rohrer ◽  
Djuro Mihelcic ◽  
Robert Wegener ◽  
...  

The analysis of the individual composition of hydrocarbon (VOC) mixtures enables us to transform observed VOC-concentrations into their respective total VOC-reactivity versus OH radicals (RVOC = Σ(kOH+VOCi × [VOCi])). This is particularly useful because local ozone production essentially depends on this single parameter rather than on the details of the underlying hydrocarbon mixture (Klemp et al., Schriften des Forschungszentrums Jülich, Energy & Environment, 2012, 21). The VOC composition also enables us to pin down the major emission source of hydrocarbons in urban areas to be petrol cars with temporarily reduced catalyst efficiency (the so-called cold-start situation) whereas the source of nitrogen oxides (NOx = NO + NO2) is expected to be nowadays dominated by diesel cars. The observations in the vicinity of main roads in German cities show a decrease in the ratio of OH reactivities of VOC and NO2 (RVOC/RNO2) by a factor of 7.5 over the time period 1994–2014. This is larger than the expected decrease of a factor of 2.9 taking estimated trends of VOC and NOx traffic emissions in Germany (Umweltbundesamt Deutschland, National Trend Tables for the German Atmospheric Emission Reporting, 2015), during this time period. The observed reduction in the RVOC/RNO2 ratio leads to a drastic decrease in local ozone production driven by the reduction in hydrocarbons. The analysis reveals that the overall reduction of ozone production benefits from the low decrease of NOx emissions from road traffic which is a consequence of the eventual absence of catalytic converters for nitrogen oxide removal in diesel cars up to now.


2013 ◽  
Vol 21 (3) ◽  
pp. 149-179 ◽  
Author(s):  
Mohanad El-Harbawi

The objective of this paper is to provide a comprehensive theoretical review with regard to history, existing approaches, recent developments, major research, associated computational methods, and applications of air quality models. A wide range of topics is covered, focusing on sources of air pollution, primary and secondary pollutants, atmospheric chemistry, atmospheric chemical transport models, computer programs for dispersion modelling, online and offline air quality modelling, data assimilation, parallel computing, applications of geographic information system in air quality modelling, air quality index, as well as the use of satellite and remote sensing data in air quality modelling. Each of these elements is comprehensively discussed, covered, and reviewed with respect to various literature and methods related to air quality modelling and applications. Several major commercial and noncommercial dispersion packages are extensively reviewed and detailed advantages and limitations of their applications are highlighted. The paper includes several comparison summaries among various models used in air quality study. Furthermore, the paper provides useful web sites, where readers can obtain further information regarding air quality models and (or) software. Lastly, current generation of air quality models and future directions are also discussed. This paper may serve as a compendium for scientists who work in air quality modelling field. Some topics are generally treated; therefore, the paper may also be used as a reference source by many scientists working with air quality modelling.


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.


2019 ◽  
Vol 177 (2) ◽  
pp. 7-11
Author(s):  
Zdzisław CHŁOPEK ◽  
Jakub LASOCKI ◽  
Katarzyna STRZAŁKOWSKA ◽  
Dagna ZAKRZEWSKA

In the large urban areas, in middle latitudes, as in case of Poland, the cause of poor air quality is immission: in winter particulate matter PM10 and PM2.5, in summer – ozone and nitrogen oxides (or nitrogen dioxide). In the whole country, road transport is significantly responsible for the emission of nitrogen oxides (30%), carbon monoxide (20%) and less for emission of particulate matter (a few percent). In the case of other pollutants, the emission of non-metallic organic compounds is less than 10% (including polycyclic organic compounds – just over 0.5%), and sulfur oxides – only 0.03%! To analyze impact of automotive industry on air quality, pollutant emission data from two stations in Krakow were selected. These stations are known for poor air quality – the stations are: Dietla Street – with a high level of traffic and Kurdwanów – place located far from traffic routes. It was found that other objects than automotive vehicles are the dominant source of dust. These are industrial sources and – above all – energy sources, especially individual heating installations. Particularly large dust pollution occurs in winter and it is not always in areas with intense traffic. There was a strong dependence between immission of pollutants and road traffic, however, this dependence is not dominant in assessing the risk of air quality in urban agglomerations.


2015 ◽  
Vol 8 (11) ◽  
pp. 3733-3746 ◽  
Author(s):  
B. Gantt ◽  
J. T. Kelly ◽  
J. O. Bash

Abstract. Sea spray aerosols (SSAs) impact the particle mass concentration and gas-particle partitioning in coastal environments, with implications for human and ecosystem health. Model evaluations of SSA emissions have mainly focused on the global scale, but regional-scale evaluations are also important due to the localized impact of SSAs on atmospheric chemistry near the coast. In this study, SSA emissions in the Community Multiscale Air Quality (CMAQ) model were updated to enhance the fine-mode size distribution, include sea surface temperature (SST) dependency, and reduce surf-enhanced emissions. Predictions from the updated CMAQ model and those of the previous release version, CMAQv5.0.2, were evaluated using several coastal and national observational data sets in the continental US. The updated emissions generally reduced model underestimates of sodium, chloride, and nitrate surface concentrations for coastal sites in the Bay Regional Atmospheric Chemistry Experiment (BRACE) near Tampa, Florida. Including SST dependency to the SSA emission parameterization led to increased sodium concentrations in the southeastern US and decreased concentrations along parts of the Pacific coast and northeastern US. The influence of sodium on the gas-particle partitioning of nitrate resulted in higher nitrate particle concentrations in many coastal urban areas due to increased condensation of nitric acid in the updated simulations, potentially affecting the predicted nitrogen deposition in sensitive ecosystems. Application of the updated SSA emissions to the California Research at the Nexus of Air Quality and Climate Change (CalNex) study period resulted in a modest improvement in the predicted surface concentration of sodium and nitrate at several central and southern California coastal sites. This update of SSA emissions enabled a more realistic simulation of the atmospheric chemistry in coastal environments where marine air mixes with urban pollution.


2017 ◽  
Vol 7 (15) ◽  
pp. 8-17 ◽  
Author(s):  
Modise Wiston

Background. Air pollution is an important issue in developed and industrialized countries. The most common sources of air pollution are anthropogenic activities such as construction dust, vehicular emissions and mining. For low- and middle-income countries, biomass burning and indoor heating are the leading sources of air pollution. As more of the world undergoes development and human populations increase, industrialization is also increasing, along with the potential for air pollution. Objectives. This article reviews the status of air pollution to raise awareness of air quality and human health in Botswana. Discussion. Since independence, Botswana has experienced one of the highest economic development growth rates in the world. These changes have occurred as a result of economic growth and resource utilization associated with increased industrialization. However, there is growing worldwide concern about the effect and impact of pollution due to industrial growth. Botswana is ranked amongst the most polluted countries with serious air pollution, despite a population of just over 2 million. Conclusions. Rapid development and increased urbanization have had a major environmental impact around the world. This increased growth has the potential to lead to air quality degradation. Significant health threats are posed by industrial and vehicular emissions, especially in urban and peri-urban areas where the population is most concentrated. It is important that the linkage between air pollution and health effects is fully examined across all scales of life, especially in developing countries. In addition, programs should be devised to educate the public about the pollution impacts on health. Competing Interests: The authors declare no financial competing interests.


2019 ◽  
Author(s):  
Matthias Karl ◽  
Sam-Erik Walker ◽  
Sverre Solberg ◽  
Martin O. P. Ramacher

Abstract. This paper describes the CityChem extension of the Eulerian urban dispersion model EPISODE. The development of the CityChem extension was driven by the need to apply the model in lower latitude cities with higher insolation than in northern European cities. The CityChem extension offers a more advanced treatment of the photochemistry in urban areas and entails specific developments within the sub-grid components for a more accurate representation of the dispersion in the proximity of urban emission sources. The WMPP (WORM Meteorological Pre-Processor) is used in the point source sub-grid model to calculate the wind speed at plume height. The simplified street canyon model (SSCM) is used in the line source sub-grid model to calculate pollutant dispersion in street canyons. The EPISODE-CityChem model integrates the CityChem extension in EPISODE, with the capability of simulating photochemistry and dispersion of multiple reactive pollutants within urban areas. The main focus of the model is the simulation of the complex atmospheric chemistry involved in the photochemical production of ozone in urban areas. EPISODE-CityChem was evaluated with a series of tests and with a first application to the air quality situation in the city of Hamburg, Germany. A performance analysis with the FAIRMODE DELTA Tool for the air quality in Hamburg showed that the model fulfils the model performance objectives for NO2 (hourly), O3 (daily max. of the 8-h running mean) and PM10 (daily mean) set forth in the Air Quality Directive, qualifying the model for use in policy applications. Observed levels of annual mean ozone at the five urban background stations in Hamburg are captured by the model within 15 %. Envisaged applications of the EPISODE-CityChem model are urban air quality studies, emission control scenarios in relation to traffic restrictions and the source attribution of sector-specific emissions to observed levels of air pollutants at urban monitoring stations.


2016 ◽  
Author(s):  
Gina M. Mazzuca ◽  
Xinrong Ren ◽  
Christopher P. Loughner ◽  
Mark Estes ◽  
James H. Crawford ◽  
...  

Abstract. An observation-constrained box model based on the Carbon Bond mechanism, Version 5 (CB05), was used to study photochemical processes along the NASA P-3B flight track and spirals over eight surface sites during the September 2013 Houston, Texas deployment of the NASA DISCOVER-AQ campaign. Data from this campaign provided an opportunity to examine and improve our understanding of atmospheric photochemical oxidation processes related to the formation of secondary air pollutants such as ozone (O3). O3 production and its sensitivity to NOx and VOCs were calculated at different locations and times of day. Ozone production efficiency (OPE), defined as the ratio of the ozone production rate to the NOx oxidation rate, was calculated using the observations and the simulation results of the box and Community Multiscale Air Quality (CMAQ) models. Correlations of these results with other parameters, such as radical sources and NOx mixing ratio, were also evaluated. It was generally found that O3 production tends to be more VOC sensitive in the morning along with high ozone production rates, suggesting that control of VOCs may be an effective way to control O3 in Houston. In the afternoon, O3 production was found to be mainly NOx sensitive with some exceptions. O3 production at near major emissions sources such as Deer Park was mostly VOC sensitive for the entire day, other urban areas near Moody Tower and Channelview were VOC sensitive or in the transition regime, and areas farther from downtown Houston such as Smith Point and Conroe were mostly NOx sensitive for the entire day. It was also found that the control of NOx emissions has reduced O3 concentrations over Houston, but led to larger OPE values. The results from this work strengthen our understanding of O3 production; they indicate that controlling NOx emissions will provide air quality benefits over the greater Houston metropolitan area in the long run, but in selected areas controlling VOC emissions will also be beneficial.


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