scholarly journals The impact of observation nudging on simulated meteorology and ozone concentrations during DISCOVER-AQ 2013 Texas campaign

2016 ◽  
Vol 16 (5) ◽  
pp. 3127-3144 ◽  
Author(s):  
Xiangshang Li ◽  
Yunsoo Choi ◽  
Beata Czader ◽  
Anirban Roy ◽  
Hyuncheol Kim ◽  
...  
Keyword(s):  
Air Quality ◽  
Low Cost ◽  
Surface Ozone ◽  
Chemical Transport ◽  
Early Morning ◽  
Small Scale ◽  
Boundary Layer Height ◽  
Ozone Concentrations ◽  
Houston Ship Channel ◽  
The Impact

Abstract. Accurate meteorological fields are imperative for correct chemical transport modeling. Observation nudging, along with objective analysis, is generally considered a low-cost and effective technique to improve meteorological simulations. However, the meteorological impact of observation nudging on chemistry has not been well characterized. This study involved two simulations to analyze the impact of observation nudging on simulated meteorology and ozone concentrations during the 2013 Deriving Information on Surface conditions from Column and Vertically Resolved Observations Relevant to Air Quality (DISCOVER-AQ) Texas campaign period, using the Weather Research and Forecasting (WRF) and Community Multiscale Air Quality (CMAQ) models. The results showed improved correlations between observed and simulated parameters. For example, the index of agreement (IOA) improved by about 9 % for surface temperature and 6–11 % for surface zonal (U-WIND) and meridional (V-WIND) winds when observation nudging was employed. Analysis of a cold front event indicated that nudging improved the timing of wind transition during the front passage. Observation nudging also reduced the model biases for the planetary boundary layer height predictions. Additionally, the IOA for CMAQ simulated surface ozone improved by 6 % during the simulation period. The high-ozone episode on 25 September was a post-front ozone event in Houston. The small-scale morning wind shifts near the Houston Ship Channel combined with higher aloft ozone early morning likely caused the day's ozone exceedance. While observation nudging did not recreate the wind shifts on that day and failed to reproduce the observed high ozone, analyses of surface and aircraft data found that observation nudging helped the model yield improved ozone predictions. In a 2 h period during the event, substantially better winds in the sensitivity case noticeably improved the ozone. The average IOA for ozone in the period increased from just over 0.4 to near 0.7. Further work on improving the capability of nudging to reproduce local meteorological events such as stagnations and wind reversals could enhance a chemical transport model's skill for predicting high-ozone events.

scholarly journals The impact of observation nudging on simulated meteorology and ozone concentrations during DISCOVER-AQ 2013 Texas campaign

2015 ◽  
Vol 15 (19) ◽  
pp. 27357-27404 ◽  
Author(s):  
X. Li ◽  
Y. Choi ◽  
B. Czader ◽  
H. Kim ◽  
B. Lefer ◽  
...  
Keyword(s):  
Air Quality ◽  
Low Cost ◽  
Surface Ozone ◽  
Small Scale ◽  
Ozone Concentrations ◽  
Simulated Surface ◽  
Houston Ship Channel ◽  
Meteorological Impact ◽  
Height Predictions ◽  
The Impact

Abstract. Air quality modeling demands accurate meteorological simulations. Observation nudging, also known as objective analysis (OA), is generally considered a low-cost and effective technique to improve meteorological simulations. However the meteorological impact of OA on chemistry has not been well characterized. This study involved two simulations (with/without OA) to analyze the impact of OA on the simulated meteorology and ozone concentrations during the Deriving Information on Surface conditions from Column and Vertically Resolved Observations Relevant to Air Quality (DISCOVER-AQ) Texas campaign period in September 2013, using Weather Research and Forecasting (WRF) and Community Multiscale Air Quality (CMAQ) models. The results showed improved correlations between observed and simulated parameters from the OA case. The index of agreement (IOA) improved by about 9 % for surface temperature and 6–11 % for surface zonal (U-WIND) and meridional (V-WIND) winds when OA was employed. Analysis of a cold front event indicated that OA improved the timing of wind transition during front passage. Employing OA also reduced the model biases in the planetary boundary height predictions. For CMAQ simulated surface ozone during the whole simulated period, IOA improved by 6 % in the OA case. The high ozone episode on 25 September was a typical post-front ozone event in Houston. The small-scale morning wind-shifts near the Houston Ship Channel combined with higher aloft ozone from recirculation likely caused the day's ozone exceedance. While OA did not reproduce the wind shifts on that day and failed to reproduce the observed surface and aloft high ozone, analyses of surface and aircraft data found that OA results matched better with observations. In a two-hour period during the event, substantially better winds in OA noticeably improved the ozone. Further work on improving OA's capability to reproduce local meteorological events could enhance a chemistry model's ability to predict high ozone events.

scholarly journals Sensitivity of Surface Ozone Simulation to Cumulus Parameterization

2008 ◽  
Vol 47 (5) ◽  
pp. 1456-1466 ◽  
Author(s):  
Zhining Tao ◽  
Allen Williams ◽  
Ho-Chun Huang ◽  
Michael Caughey ◽  
Xin-Zhong Liang
Keyword(s):  
Cloud Cover ◽  
Surface Ozone ◽  
Meteorological Conditions ◽  
Cumulus Parameterization ◽  
Daily Maximum ◽  
Boundary Layer Height ◽  
Ozone Concentrations ◽  
Simulated Precipitation ◽  
Cumulus Schemes ◽  
The Impact

Abstract Different cumulus schemes cause significant discrepancies in simulated precipitation, cloud cover, and temperature, which in turn lead to remarkable differences in simulated biogenic volatile organic compound (BVOC) emissions and surface ozone concentrations. As part of an effort to investigate the impact (and its uncertainty) of climate changes on U.S. air quality, this study evaluates the sensitivity of BVOC emissions and surface ozone concentrations to the Grell (GR) and Kain–Fritsch (KF) cumulus parameterizations. Overall, using the KF scheme yields less cloud cover, larger incident solar radiation, warmer surface temperature, and higher boundary layer height and hence generates more BVOC emissions than those using the GR scheme. As a result, the KF (versus GR) scheme produces more than 10 ppb of summer mean daily maximum 8-h ozone concentration over broad regions, resulting in a doubling of the number of high-ozone occurrences. The contributions of meteorological conditions versus BVOC emissions on regional ozone sensitivities to the choice of the cumulus scheme largely offset each other in the California and Texas regions, but the contrast in BVOC emissions dominates over that in the meteorological conditions for ozone differences in the Midwest and Northeast regions. The result demonstrates the necessity of considering the uncertainty of future ozone projections that are identified with alternative model physics configurations.

scholarly journals Solar “brightening” impact on summer surface ozone between 1990 and 2010 in Europe – a model sensitivity study of the influence of the aerosol–radiation interactions

2018 ◽  
Vol 18 (13) ◽  
pp. 9741-9765 ◽  
Author(s):  
Emmanouil Oikonomakis ◽  
Sebnem Aksoyoglu ◽  
Martin Wild ◽  
Giancarlo Ciarelli ◽  
Urs Baltensperger ◽  
...  
Keyword(s):  
Air Quality ◽  
Surface Ozone ◽  
Biogenic Emissions ◽  
Base Case ◽  
Air Quality Model ◽  
Quality Model ◽  
Ozone Concentrations ◽  
Photolysis Rates ◽  
Ozone Trends ◽  
The Impact

Abstract. Surface solar radiation (SSR) observations have indicated an increasing trend in Europe since the mid-1980s, referred to as solar “brightening”. In this study, we used the regional air quality model, CAMx (Comprehensive Air Quality Model with Extensions) to simulate and quantify, with various sensitivity runs (where the year 2010 served as the base case), the effects of increased radiation between 1990 and 2010 on photolysis rates (with the PHOT1, PHOT2 and PHOT3 scenarios, which represented the radiation in 1990) and biogenic volatile organic compound (BVOC) emissions (with the BIO scenario, which represented the biogenic emissions in 1990), and their consequent impacts on summer surface ozone concentrations over Europe between 1990 and 2010. The PHOT1 and PHOT2 scenarios examined the effect of doubling and tripling the anthropogenic PM2.5 concentrations, respectively, while the PHOT3 investigated the impact of an increase in just the sulfate concentrations by a factor of 3.4 (as in 1990), applied only to the calculation of photolysis rates. In the BIO scenario, we reduced the 2010 SSR by 3 % (keeping plant cover and temperature the same), recalculated the biogenic emissions and repeated the base case simulations with the new biogenic emissions. The impact on photolysis rates for all three scenarios was an increase (in 2010 compared to 1990) of 3–6 % which resulted in daytime (10:00–18:00 Local Mean Time – LMT) mean surface ozone differences of 0.2–0.7 ppb (0.5–1.5 %), with the largest hourly difference rising as high as 4–8 ppb (10–16 %). The effect of changes in BVOC emissions on daytime mean surface ozone was much smaller (up to 0.08 ppb, ∼ 0.2 %), as isoprene and terpene (monoterpene and sesquiterpene) emissions increased only by 2.5–3 and 0.7 %, respectively. Overall, the impact of the SSR changes on surface ozone was greater via the effects on photolysis rates compared to the effects on BVOC emissions, and the sensitivity test of their combined impact (the combination of PHOT3 and BIO is denoted as the COMBO scenario) showed nearly additive effects. In addition, all the sensitivity runs were repeated on a second base case with increased NOx emissions to account for any potential underestimation of modeled ozone production; the results did not change significantly in magnitude, but the spatial coverage of the effects was profoundly extended. Finally, the role of the aerosol–radiation interaction (ARI) changes in the European summer surface ozone trends was suggested to be more important when comparing to the order of magnitude of the ozone trends instead of the total ozone concentrations, indicating a potential partial damping of the effects of ozone precursor emissions' reduction.

scholarly journals Modeling the impact of solar brightening on summer surface ozone over Europe between 1990 and 2010

2018 ◽  
Author(s):  
Emmanouil Oikonomakis ◽  
Sebnem Aksoyoglu ◽  
Martin Wild ◽  
Giancarlo Ciarelli ◽  
Urs Baltensperger ◽  
...  
Keyword(s):  
Air Quality ◽  
Surface Ozone ◽  
Biogenic Emissions ◽  
Base Case ◽  
Air Quality Model ◽  
Quality Model ◽  
Ozone Concentrations ◽  
Photolysis Rates ◽  
Ozone Trends ◽  
The Impact

Abstract. Surface solar radiation (SSR) observations have indicated an increasing trend in Europe since the mid-1980s, referred to as solar brightening. In this study, we used the regional air quality model, CAMx (Comprehensive Air Quality Model with extensions) to simulate and quantify, with various sensitivity runs (where the year 2010 served as the base case), the effects of increased radiation on photolysis rates (PHOT1, PHOT2 and PHOT3 scenarios) and biogenic volatile organic compounds (BVOCs) emissions (BIO scenario), and their consequent impacts on summer surface ozone concentrations over Europe between 1990 and 2010. The PHOT1 and PHOT2 scenarios examined the effect of doubling and tripling the anthropogenic PM2.5 concentrations, respectively, while the PHOT3 investigated the impact of an increase in just the sulfate concentrations by a factor of 3.4 (as in 1990), applied only to the calculation of photolysis rates. In the BIO scenario, we reduced the 2010 SSR by 3 % (keeping plant cover and temperature the same), re-calculated the biogenic emissions and repeated the base case simulations with the new biogenic emissions. The impact on photolysis rates for all three scenarios was an increase (in 2010 compared to 1990) of 3–6 % which resulted in daytime (10:00–18:00 Local Mean Time (LMT)) mean surface ozone differences of 0.2–0.7 ppb (0.5–1.5 %), with the largest hourly difference rising as high as 4–8 ppb (10–16 %). The effect of changes in BVOCs emissions on daytime mean surface ozone was much smaller (up to 0.08 ppb, ~ 0.2 %), as isoprene and terpene (monoterpene and sesquiterpene) emissions increased only by 2.5–3 % and 0.7 %, respectively. Overall, the impact of the SSR changes on surface ozone was greater via the effects on photolysis rates compared to the effects on BVOCs emissions, and the sensitivity test of their combined impact (PHOT3 + BIO = COMBO scenario) showed nearly additive effects. In addition, all the sensitivity runs were repeated on a second base case with increased NOx emissions to account for any potential underestimation of modeled ozone production; the results did not change significantly in magnitude, but the spatial coverage of the effects was profoundly extended. Finally, the role of the solar brightening in the European summer surface ozone trends was suggested to be more important when comparing to the order of magnitude of the ozone trends instead of the total ozone concentrations, indicating a potential partial damping of the effects of ozone precursor emissions reduction.

scholarly journals Developing Relative Humidity and Temperature Corrections for Low-Cost Sensors Using Machine Learning

Sensors ◽  
2021 ◽  
Vol 21 (10) ◽  
pp. 3338
Author(s):  
Ivan Vajs ◽  
Dejan Drajic ◽  
Nenad Gligoric ◽  
Ilija Radovanovic ◽  
Ivan Popovic
Keyword(s):  
Machine Learning ◽  
Air Quality ◽  
Relative Humidity ◽  
Low Cost ◽  
Quality Monitoring ◽  
Air Quality Monitoring ◽  
Lower Accuracy ◽  
Wide Range ◽  
The Impact ◽  
Monitoring Stations

Existing government air quality monitoring networks consist of static measurement stations, which are highly reliable and accurately measure a wide range of air pollutants, but they are very large, expensive and require significant amounts of maintenance. As a promising solution, low-cost sensors are being introduced as complementary, air quality monitoring stations. These sensors are, however, not reliable due to the lower accuracy, short life cycle and corresponding calibration issues. Recent studies have shown that low-cost sensors are affected by relative humidity and temperature. In this paper, we explore methods to additionally improve the calibration algorithms with the aim to increase the measurement accuracy considering the impact of temperature and humidity on the readings, by using machine learning. A detailed comparative analysis of linear regression, artificial neural network and random forest algorithms are presented, analyzing their performance on the measurements of CO, NO2 and PM10 particles, with promising results and an achieved R2 of 0.93–0.97, 0.82–0.94 and 0.73–0.89 dependent on the observed period of the year, respectively, for each pollutant. A comprehensive analysis and recommendations on how low-cost sensors could be used as complementary monitoring stations to the reference ones, to increase spatial and temporal measurement resolution, is provided.

scholarly journals Modelling the impact of megacities on local, regional and global tropospheric ozone and the deposition of nitrogen species

2013 ◽  
Vol 13 (24) ◽  
pp. 12215-12231 ◽  
Author(s):  
Z. S. Stock ◽  
M. R. Russo ◽  
T. M. Butler ◽  
A. T. Archibald ◽  
M. G. Lawrence ◽  
...  
Keyword(s):  
Air Quality ◽  
Urban Areas ◽  
Climate Model ◽  
Surface Ozone ◽  
Global Scale ◽  
Chemical Environment ◽  
Ozone Production ◽  
The Uk ◽  
The Impact ◽  
Local Emissions

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.

Temporal patterns and trends of surface ozone concentrations over Portugal

2021 ◽  
Author(s):  
Carla Gama ◽  
Alexandra Monteiro ◽  
Myriam Lopes ◽  
Ana Isabel Miranda
Keyword(s):  
Air Quality ◽  
Iberian Peninsula ◽  
Human Health ◽  
Temporal Variability ◽  
Urban Areas ◽  
Surface Ozone ◽  
Quality Data ◽  
Ozone Concentrations ◽  
Long Term Study

<p>Tropospheric ozone (O<sub>3</sub>) is a critical pollutant over the Mediterranean countries, including Portugal, due to systematic exceedances to the thresholds for the protection of human health. Due to the location of Portugal, on the Atlantic coast at the south-west point of Europe, the observed O<sub>3</sub> concentrations are very much influenced not only by local and regional production but also by northern mid-latitudes background concentrations. Ozone trends in the Iberian Peninsula were previously analysed by Monteiro et al. (2012), based on 10-years of O<sub>3</sub> observations. Nevertheless, only two of the eleven background monitoring stations analysed in that study are located in Portugal and these two stations are located in Porto and Lisbon urban areas. Although during pollution events O<sub>3</sub> levels in urban areas may be high enough to affect human health, the highest concentrations are found in rural locations downwind from the urban and industrialized areas, rather than in cities. This happens because close to the sources (e.g., in urban areas) freshly emitted NO locally scavenges O<sub>3</sub>. A long-term study of the spatial and temporal variability and trends of the ozone concentrations over Portugal is missing, aiming to answer the following questions:</p><p>-           What is the temporal variability of ozone concentrations?</p><p>-           Which trends can we find in observations?</p><p>-           How were the ozone spring maxima concentrations affected by the COVID-19 lockdown during spring 2020?</p><p>In this presentation, these questions will be answered based on the statistical analysis of O<sub>3</sub> concentrations recorded within the national air quality monitoring network between 2005 and 2020 (16 years). The variability of the surface ozone concentrations over Portugal, on the timescales from diurnal to annual, will be presented and discussed, taking into account the physical and chemical processes that control that variability. Using the TheilSen function from the OpenAir package for R (Carslaw and Ropkins 2012), which quantifies monotonic trends and calculates the associated p-value through bootstrap simulations, O<sub>3</sub> concentration long-term trends will be estimated for the different regions and environments (e.g., rural, urban).  Moreover, taking advantage of the unique situation provided by the COVID-19 lockdown during spring 2020, when the government imposed mandatory confinement and citizens movement restriction, leading to a reduction in traffic-related atmospheric emissions, the role of these emissions on ozone levels during the spring period will be studied and presented.</p><p> </p><p>Carslaw and Ropkins, 2012. Openair—an R package for air quality data analysis. Environ. Model. Softw. 27-28,52-61. https://doi.org/10.1016/j.envsoft.2011.09.008</p><p>Monteiro et al., 2012. Trends in ozone concentrations in the Iberian Peninsula by quantile regression and clustering. Atmos. Environ. 56, 184-193. https://doi.org/10.1016/j.atmosenv.2012.03.069</p>

scholarly journals Entrainment and Mixing of Transported Ozone Layers: Implications for Surface Air Quality in the Western U.S.

2020 ◽  
Vol 237 ◽  
pp. 03012
Author(s):  
Christoph Senff ◽  
Andrew Langford ◽  
Raul Alvarez ◽  
Tim Bonin ◽  
Alan Brewer ◽  
...  
Keyword(s):  
Boundary Layer ◽  
Air Quality ◽  
Mixed Layer ◽  
Las Vegas ◽  
Surface Ozone ◽  
Ground Level ◽  
San Joaquin Valley ◽  
Fire Emissions ◽  
Ozone Transport ◽  
The Impact

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.

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 Impacts of changes in land use and land cover on atmospheric chemistry and air quality over the 21st century

2011 ◽  
Vol 11 (5) ◽  
pp. 15469-15495 ◽  
Author(s):  
S. Wu ◽  
L. J. Mickley ◽  
J. O. Kaplan ◽  
D. J. Jacob
Keyword(s):  
Land Use ◽  
Air Quality ◽  
Land Use Change ◽  
Land Cover ◽  
21St Century ◽  
Secondary Organic Aerosols ◽  
Surface Ozone ◽  
Organic Aerosols ◽  
Ozone Concentrations ◽  
Anthropogenic Land Use

Abstract. The effects of future land use and land cover change on the chemical composition of the atmosphere and air quality are largely unknown. To investigate the potential effects associated with future changes in vegetation driven by atmospheric CO2 concentrations, climate, and anthropogenic land use over the 21st century, we performed a series of model experiments combining a general circulation model with a dynamic global vegetation model and an atmospheric chemical-transport model. Our results indicate that climate- and CO2-induced changes in vegetation composition and density could lead to decreases in summer afternoon surface ozone of up to 10 ppb over large areas of the northern mid-latitudes. This is largely driven by the substantial increases in ozone dry deposition associated with changes in the composition of temperate and boreal forests where conifer forests are replaced by those dominated by broadleaf tree types, as well as a CO2-driven increase in vegetation density. Climate-driven vegetation changes over the period 2000–2100 lead to general increases in isoprene emissions, globally by 15 % in 2050 and 36 % in 2100. These increases in isoprene emissions result in decreases in surface ozone concentrations where the NOx levels are low, such as in remote tropical rainforests. However, over polluted regions, such as the northeastern United States, ozone concentrations are calculated to increase with higher isoprene emissions in the future. Increases in biogenic emissions also lead to higher concentrations of secondary organic aerosols, which increase globally by 10 % in 2050 and 20 % in 2100. Surface concentrations of secondary organic aerosols are calculated to increase by up to 1 μg m−3 for large areas in Eurasia. When we use a scenario of future anthropogenic land use change, we find less increase in global isoprene emissions due to replacement of higher-emitting forests by lower-emitting cropland. The global atmospheric burden of secondary organic aerosols changes little by 2100 when we account for future land use change, but both secondary organic aerosols and ozone show large regional changes at the surface.

Sign in / Sign up

Export Citation Format

Share Document