scholarly journals Updating sea spray aerosol emissions in the Community Multiscale Air Quality (CMAQ) model version 5.0.2

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.

2015 ◽  
Vol 8 (5) ◽  
pp. 3905-3939 ◽  
Author(s):  
B. Gantt ◽  
J. T. Kelly ◽  
J. O. Bash

Abstract. Sea spray aerosols (SSA) impact the particle mass concentration and gas-particle partitioning in coastal environments, with implications for human and ecosystem health. Despite their importance, the emission magnitude of SSA remains highly uncertain with global estimates varying by nearly two orders of magnitude. In this study, the Community Multiscale Air Quality (CMAQ) model was updated to enhance fine mode SSA emissions, include sea surface temperature (SST) dependency, and reduce coastally-enhanced emissions. Predictions from the updated CMAQ model and those of the previous release version, CMAQv5.0.2, were evaluated using several regional and national observational datasets in the continental US. The updated emissions generally reduced model underestimates of sodium, chloride, and nitrate surface concentrations for an inland site of 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 southeast 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 modest improvement in the predicted surface concentration of sodium and nitrate at several central and southern California coastal sites. This SSA emission update enabled a more realistic simulation of the atmospheric chemistry in environments where marine air mixes with urban pollution.


Atmosphere ◽  
2021 ◽  
Vol 12 (2) ◽  
pp. 264 ◽  
Author(s):  
Giovanni Lonati ◽  
Federico Riva

The impact of the reduced atmospheric emissions due to the COVID-19 lockdown on ambient air quality in the Po Valley of Northern Italy was assessed for gaseous pollutants (NO2, benzene, ammonia) based on data collected at the monitoring stations distributed all over the area. Concentration data for each month of the first semester of 2020 were compared with those of the previous six years, on monthly, daily, and hourly bases, so that pre, during, and post-lockdown conditions of air quality could be separately analyzed. The results show that, as in many other areas worldwide, the Po Valley experienced better air quality during 2020 spring months for NO2 and benzene. In agreement with the reductions of nitrogen oxides and benzene emissions from road traffic, estimated to be −35% compared to the regional average, the monthly mean concentration levels for 2020 showed reductions in the −40% to −35% range compared with the previous years, but with higher reductions, close to −50%, at high-volume-traffic sites in urban areas. Conversely, NH3 ambient concentration levels, almost entirely due the emissions of the agricultural sector, did not show any relevant change, even at high-volume-traffic sites in urban areas. These results point out the important role of traffic emissions in NO2 and benzene ambient levels in the Po Valley, and confirm that this region is a rather homogeneous air basin with urban area hot-spots, the contributions of which add up to a relatively high regional background concentration level. Additionally, the relatively slow response of the air quality levels to the sudden decrease of the emissions due to the lockdown shows that this region is characterized by a weak exchange of the air masses that favors both the build-up of atmospheric pollutants and the development of secondary formation processes. Thus, air quality control strategies should aim for structural interventions intended to reduce traffic emissions at the regional scale and not only in the largest urban areas.


Atmosphere ◽  
2021 ◽  
Vol 12 (4) ◽  
pp. 431
Author(s):  
Ayako Yoshino ◽  
Akinori Takami ◽  
Keiichiro Hara ◽  
Chiharu Nishita-Hara ◽  
Masahiko Hayashi ◽  
...  

Transboundary air pollution (TAP) and local air pollution (LAP) influence the air quality of urban areas. Fukuoka, located on the west side of Japan and affected by TAP from the Asian continent, is a unique example for understanding the contribution of LAP and TAP. Gaseous species and particulate matter (PM) were measured for approximately three weeks in Fukuoka in the winter of 2018. We classified two distinctive periods, LAP and TAP, based on wind speed. The classification was supported by variations in the concentration of gaseous species and by backward trajectories. Most air pollutants, including NOx and PM, were high in the LAP period and low in the TAP period. However, ozone was the exception. Therefore, our findings suggest that reducing local emissions is necessary. Ozone was higher in the TAP period, and the variation in ozone concentration was relatively small, indicating that ozone was produced outside of the city and transported to Fukuoka. Thus, air pollutants must also be reduced at a regional scale, including in China.


2010 ◽  
Vol 10 (15) ◽  
pp. 7415-7423 ◽  
Author(s):  
B. Gantt ◽  
N. Meskhidze ◽  
A. G. Carlton

Abstract. The contribution of marine organic emissions to the air quality in coastal areas of the western United States is studied using the latest version of the US Environmental Protection Agency (EPA) regional-scale Community Multiscale Air Quality (CMAQv4.7) modeling system. Emissions of marine isoprene, monoterpenes, and primary organic matter (POM) from the ocean are implemented into the model to provide a comprehensive view of the connection between ocean biology and atmospheric chemistry and air pollution. Model simulations show that marine organics can increase the concentration of PM2.5 by 0.1–0.3 μg m−3 (up to 5%) in some coastal cities such as San Francisco, CA. This increase in the PM2.5 concentration is primarily attributed to the POM emissions, with small contributions from the marine isoprene and monoterpenes. When marine organic emissions are included, organic carbon (OC) concentrations over the remote ocean are increased by up to 50% (25% in coastal areas), values consistent with recent observational findings. This study is the first to quantify the air quality impacts from marine POM and monoterpenes for the United States, and it highlights the need for inclusion of marine organic emissions in air quality models.


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):  
Efisio Solazzo ◽  
Roberto Bianconi ◽  
Christian Hogrefe ◽  
Gabriele Curci ◽  
Ummugulsum Alyuz ◽  
...  

Abstract. Through the comparison of several regional-scale chemistry transport modelling systems that simulate meteorology and air quality over the European and American continents, this study aims at i) apportioning the error to the responsible processes using time-scale analysis, ii) helping to detect causes of models error, and iii) identifying the processes and scales most urgently requiring dedicated investigations. The analysis is conducted within the framework of the third phase of the Air Quality Model Evaluation International Initiative (AQMEII) and tackles model performance gauging through measurement-to-model comparison, error decomposition and time series analysis of the models biases for several fields (ozone, CO, SO2, NO, NO2, PM10, PM2.5, wind speed, and temperature). The operational metrics (magnitude of the error, sign of the bias, associativity) provide an overall sense of model strengths and deficiencies, while apportioning the error to its constituent parts (bias, variance and covariance) can help to assess the nature and quality of the error. Each of the error components is analysed independently and apportioned to specific processes based on the corresponding timescale (long scale, synoptic, diurnal, and intra-day) using the error apportionment technique devised in the former phases of AQMEII. The application of the error apportionment method to the AQMEII Phase 3 simulations provides several key insights. In addition to reaffirming the strong impact of model inputs (emissions and boundary conditions) and poor representation of the stable boundary layer on model bias, results also highlighted the high inter-dependencies among meteorological and chemical variables, as well as among their errors. This indicates that the evaluation of air quality model performance for individual pollutants needs to be supported by complementary analysis of meteorological fields and chemical precursors to provide results that are more insightful from a model development perspective. The error embedded in the emissions is dominant for primary species (CO, PM, NO) and largely outweighs the error from any other source. The uncertainty in meteorological fields is most relevant to ozone. Some further aspects emerged whose interpretation requires additional consideration, such as, among others, the uniformity of the synoptic error being region and model-independent, observed for several pollutants; the source of unexplained variance for the diurnal component; and the type of error caused by deposition and at which scale.


2016 ◽  
Vol 189 ◽  
pp. 277-290 ◽  
Author(s):  
Spyros N. Pandis ◽  
Ksakousti Skyllakou ◽  
Kalliopi Florou ◽  
Evangelia Kostenidou ◽  
Christos Kaltsonoudis ◽  
...  

Five case studies (Athens and Paris in Europe, Pittsburgh and Los Angeles in the United States, and Mexico City in Central America) are used to gain insights into the changing levels, sources, and role of atmospheric chemical processes in air quality in large urban areas as they develop technologically. Fine particulate matter is the focus of our analysis. In all cases reductions of emissions by industrial and transportation sources have resulted in significant improvements in air quality during the last few decades. However, these changes have resulted in the increasing importance of secondary particulate matter (PM) which dominates over primary in most cases. At the same time, long range transport of secondary PM from sources located hundreds of kilometres from the cities is becoming a bigger contributor to the urban PM levels in all seasons. “Non-traditional” sources including cooking, and residential and agricultural biomass burning contribute an increasing fraction of the now reduced fine PM levels. Atmospheric chemistry is found to change the chemical signatures of a number of these sources relatively fast both during the day and night, complicating the corresponding source apportionment.


2009 ◽  
Vol 12 (2) ◽  
pp. 111-120
Author(s):  
Nghiem Hoang Le ◽  
Oanh Thi Kim Nguyen

Long range transport of ozone and its precursors can significantly impact the air quality in downwind regions. The problem of regional transport of ozone has been studied for more than three decades in Europe and U.S but not yet in Southeast Asia. This study investigated the regional scale distribution of tropospheric ozone over the Continental South East Asia Region (CSEA) of Thailand, Burma, Cambodia, Lao and Vietnam. The Models-3 Community Multi-scale Air Quality (CMAQ modeling system, driven by the NCAR/Penn State Fifth-Generation Mesoscale Model (MM5), is used for the purpose. The model domain covers the longitude range from 91'E to 111°E and the latitude range from 5°N to 25°N. Two most recent ozone episodes of March 24-26, 2004 and January 2-4, 2005 were selected which represent the typical meteorological conditions for high ozone concentrations periods of a year. The episode analysis was made based on available data from 10 and 4 monitoring stations located in Bangkok of Thailand and Ho Chi Minh City (HCMC) of Vietnam, respectively. The episodes were characterized with hourly ozone levels above the National Ambient Air Quality Standards of Thailand and Vietnam of 100 ppb at a number of the monitoring stations. The maximum ground level concentrations of ozone for March 2004 and January 2005 episodes reached 173 ppb and 157 ppb, respectively, in the urban plume of the Bangkok Metropolitan Region (BMR). The simulations were performed with 0.5o 0.5° emission input data which was prepared from the regional anthropogenic emission inventory used in the Transport and Chemical Evolution over the Pacific (TRACE-P), and the biogenic emissions obtained from the Global Emissions Inventory Activity (GEIA). The simulated overall picture of ground level ozone concentrations over CSEA domain shows that the concentrations were high at the downwind areas at a considerable distance from large urban areas such as BMR and HCMC. During March 2004 episode the ozone plume moved northeastward following the Southwesterly monsoon and the maximum width of the modeled plume with the ozone above 100 ppb was about 70 km from BMR. For HCMC the ozone plume moved northward and the concentration in the city plume was lower with the width of isopleth of 50ppb of around 40 km. During the Jan 2005 episode the ozone plume moved southwestward following the Northeasterly monsoon and the width of the modeled plume with the ozone concentration above 100 ppb in BMR was 50 km while for HCMC the width of the 40ppb isopleth was about 30 km. The model performance was evaluated on the available observed hourly ozone concentrations. The model system was shown to be able to reproduce the peak ozone levels that occurred during the episodes at these two large urban areas, and capture the day by day variations during the selected episodes. The performance statistics MNBE, NGE, and UPA for the simulated ozone concentrations are within U.S. EPA guidance criteria and are comparable to those reported previous for other regional ozone simulations. It is shown that the MM5/CMAQ system is the suitable modeling tools for ozone prediction over the CSEA.


Author(s):  
Janet E. Nichol ◽  
Muhammad Bilal ◽  
Majid Nazeer ◽  
Man Sing Wong

AbstractThis chapter depicts the state of the art in remote sensing for urban pollution monitoring, including urban heat islands, urban air quality, and water quality around urban coastlines. Recent developments in spatial and temporal resolutions of modern sensors, and in retrieval methodologies and gap-filling routines, have increased the applicability of remote sensing for urban areas. However, capturing the spatial heterogeneity of urban areas is still challenging, given the spatial resolution limitations of aerosol retrieval algorithms for air-quality monitoring, and of modern thermal sensors for urban heat island analysis. For urban coastal applications, water-quality parameters can now be retrieved with adequate spatial and temporal detail even for localized phenomena such as algal blooms, pollution plumes, and point pollution sources. The chapter reviews the main sensors used, and developments in retrieval algorithms. For urban air quality the MODIS Dark Target (DT), Deep Blue (DB), and the merged DT/DB algorithms are evaluated. For urban heat island and urban climatic analysis using coarse- and medium- resolution thermal sensors, MODIS, Landsat, and ASTER are evaluated. For water-quality monitoring, medium spatial resolution sensors including Landsat, HJ1A/B, and Sentinel 2, are evaluated as potential replacements for expensive routine ship-borne monitoring.


2021 ◽  
Author(s):  
Peter Huszar ◽  
Jan Karlický ◽  
Jana Marková ◽  
Tereza Nováková ◽  
Marina Liaskoni ◽  
...  

Abstract. Urban areas are hot-spots of intense emissions and they influence air-quality not only locally but on regional or even global scales. The impact of urban emissions over different scales depends on the dilution and chemical transformation of the urban plumes which are governed by the local and regional scale meteorological conditions. These are influenced by the presence of urbanized land-surface via the so called urban canopy meteorological forcing (UCMF). In this study, we investigate for selected central European cities (Berlin, Budapest, Munich, Prague, Vienna and Warsaw), how the urban emission impact (UEI) is modulated by the UCMF for present day climate conditions (2015–2016) using three regional climate-chemistry models: the regional climate models RegCM and WRF-Chem (its meteorological part), the chemistry transport model CAMx coupled to either RegCM and WRF and the “chemical” component of WRF-Chem. The UCMF was calculated by replacing the urbanized surface by rural one while the UEI was estimated by removing all anthropogenic emissions from the selected cities. We analyzed the urban emissions induced changes of near surface concentrations of NO2, O3 and PM2.5. We found increases of NO2 and PM2.5 concentrations over cities by 4–6 ppbv, and 4–6 μgm−3, respectively meaning that about 40–60 % and 20–40 % of urban concentrations of NO2 and PM2.5 are caused by local emissions and the rest is the result of emissions from surrounding rural areas. We showed that if UCMF is included, the UEI of these pollutants is about 40–60 % smaller, or in other words, the urban emission impact is overestimated if urban canopy effects are not taken into account. In case of ozone, models due to UEI usually predict decreases around −2 to −4 ppbv (about 10–20 %), which is again smaller if UCMF is considered (by about 60 %). We further showed that the impact on extreme (95th percentile) air-pollution is much stronger, as well as the modulation of UEI is larger for such situations. Finally, we evaluated the contribution of the urbanization induced modifications of vertical eddy-diffusion to the modulation of UEI, and found that it alone is able to explain the modelled decrease of the urban emission impact if the effects of UCMF are considered. In summary, our results showed that the meteorological changes resulting from urbanization have to be included in regional model studies if they intend to quantify the regional fingerprint of urban emissions. Ignoring these meteorological changes can lead to strong overestimation of UEI.


Sign in / Sign up

Export Citation Format

Share Document