scholarly journals Analysis of a summer smog episode in the Berlin-Brandenburg region with a nested atmosphere -- chemistry model

2002 ◽  
Vol 2 (4) ◽  
pp. 259-270 ◽  
Author(s):  
S. E. Bauer ◽  
B. Langmann

Abstract. An analysis of a pollution episode in an urban atmosphere, using a complex model system is presented. The nested atmosphere-chemistry model system simulates the atmospheric conditions during a one week measurement campaign, called FLUMOB, in July 1994 in Berlin-Brandenburg, Germany. The analysis shows that naturally emitted hydrocarbons played the dominant role in the ozone formation in the investigated area. The composition of non-methane volatile organic compounds was made up to 70--80% by biogenically emitted hydrocarbons. During the analysed case, ozone formation was sensitive to hydrocarbon concentrations so that the ozone production was limited by the availability of hydrocarbons and thus especially by the amount which was biogenically emitted. Furthermore, it is shown that the FLUMOB episode was influenced by elevated concentrations of ozone in the free troposphere. In contrast to previous analyses, the importance of ozone produced outside of Europe is emphasized. In spite of the stagnant high pressure situation which occurred during the FLUMOB episode Germany was significantly influenced by long-range transport of ozone. This transport also influenced near surface ozone concentrations.

2002 ◽  
Vol 2 (3) ◽  
pp. 789-824 ◽  
Author(s):  
S. E. Bauer ◽  
B. Langmann

Abstract. An analysis of a pollution episode in an urban atmosphere, using a complex model system is presented. The nested atmosphere-chemistry model system simulates the atmospheric conditions during a one week measurement campaign, called FLUMOB, in July 1994 in Berlin-Brandenburg, Germany. The analysis shows that naturally emitted hydrocarbons played the dominant role in the ozone formation in the investigated area. The composition of non-methane volatile organic compounds was made up to 70--80% by biogenically emitted hydrocarbons. During the analysed case, ozone formation was sensitive to hydrocarbon concentrations so that the ozone production was limited by the availability of hydrocarbons and thus especially by the amount which was biogenically emitted. Furthermore, it is shown that the FLUMOB episode was influenced by elevated concentrations of ozone in the free troposphere. In contrast to previous analyses, the importance of ozone produced outside of Europe is emphasized. In spite of the stagnant high pressure situation which occurred during the FLUMOB episode Germany was significantly influenced by long-range transport of ozone. This transport also influenced near surface ozone concentrations.


2019 ◽  
Vol 12 (1) ◽  
pp. 363-370 ◽  
Author(s):  
Betsy M. Farris ◽  
Guillaume P. Gronoff ◽  
William Carrion ◽  
Travis Knepp ◽  
Margaret Pippin ◽  
...  

Abstract. During the 2017 Ozone Water Land Environmental Transition Study (OWLETS), the Langley mobile ozone lidar system utilized a new small diameter receiver to improve the retrieval of near-surface signals from 0.1 to 1 km in altitude. This new receiver utilizes a single 90 ∘ fiber-coupled, off-axis parabolic mirror resulting in a compact form that is easy to align. The single reflective surface offers the opportunity to easily expand its use to multiple wavelengths for additional measurement channels such as visible wavelength aerosol measurements. Detailed results compare the performance of the receiver to both ozonesonde and in situ measurements from a UAV platform, validating the performance of the near-surface ozone retrievals. Absolute O3 differences averaged 7 % between lidar and ozonesonde data from 0.1 to 1.0 km and yielded a 2.3 % high bias in the lidar data, well within the uncertainty of the sonde measurements. Conversely, lidar O3 measurements from 0.1 to 0.2 km averaged 10.5 % lower than coincident UAV O3. A more detailed study under more stable atmospheric conditions would be necessary to resolve the residual instrument differences reported in this work. Nevertheless, this unique added capability is a significant improvement allowing for near-surface observation of ozone.


2020 ◽  
Author(s):  
José M. Garrido-Pérez ◽  
Carlos Ordóñez ◽  
Ricardo García-Herrera ◽  
Jordan L. Schnell

<p>Daily maximum temperature is known to be the meteorological variable that mostly controls the afternoon near-surface ozone concentrations during summer. Air stagnation situations, characterised by stable weather conditions and poor ventilation, also lead to the accumulation of pollutants and regional ozone production close to the surface. This work evaluates the joint effect of daily maximum temperature and a simplified air stagnation index on surface ozone observations in eight regions of Europe during summer 1998-2015.</p><p>As expected, the correlations of MDA8 O<sub>3</sub> (maximum daily 8-h running average ozone) with temperature are higher than with stagnation for most regions. Nevertheless, stagnation can also be considered as a good predictor of ozone, especially in the regions of central/southern Europe, where the correlation coefficients between MDA8 O<sub>3</sub> and the percentage of stagnant area are within the range 0.50–0.70. MDA8 O<sub>3</sub> consistently increases over central/southern Europe under stagnant conditions, but this is not always the case in the north. Under non-stagnant conditions and daily maximum temperatures within 20-25 ºC (typical temperatures of fair weather conditions that allow photochemical production), northern Europe is affected by southerly advection that often brings aged air masses from more polluted areas, increasing the MDA8 O<sub>3</sub> mixing ratios.</p><p>We have also found that the ozone diurnal cycles in the central/southern regions exhibit large amplitudes, with above-average daytime and below-average night-time concentrations, when stagnation occurs. Stagnant nights are often associated with stable shallow planetary boundary layer and, presumably, enhanced dry deposition and chemical destruction of ozone. After sunrise, mixing with air from air from the residual layer, accumulation of ozone and precursors, and photochemical production seem to be the main mechanisms involved in the build-up of daytime ozone.</p><p>According to previous studies, some of the central/southern European regions where stagnation has a clear impact on ozone have undergone significant upward trends in air stagnation in the past and are also likely to experience increases in the future. However, our study has identified other regions with unclear responses of summer ozone to the occurrence of stagnation. This indicates that climate model projections of increases in stagnation should not directly be translated into enhanced summer ozone pollution if the sensitivity of this pollutant to stagnation has not been proved for a particular region.</p>


2020 ◽  
Author(s):  
Yury Shtabkin ◽  
Konstantin Moiseenko ◽  
Andrey Skorokhod ◽  
Elena Berezina

<p>Effect of photochemically active species emissions on near-surface air composition in industrial regions is non-local and in many cases can be traced in transcontinental scale. Largescaled plumes of polluted air defined by observations of tracer species on background stations and calculations with chemical-transport models are examples of this effect. In this work we use GEOS-Chem chemical transport model to make an assessment of influence have anthropogenic and biogenic emissions in Europe, European territory of Russia (ETR) and Siberia on total ozone generation taking into account common non-linear properties of O<sub>3</sub>–NO<sub>x</sub>–СО–VOC system. It is shown that increasing of ozone production rate due to regional anthropogenic emissions of NO<sub>x</sub> leads to substantial (up to 20 ppbv) increase of near-surface ozone concentrations in mid-latitudes traced up to 120E. The predominant role of long-range air transport against regional sources of photochemical ozone production was determined for the most part of European Russia and Siberia.<br>We also make a numerical assessment of ozone balance in Europe, ETR and Siberia. Annual ozone total mass in lower troposphere (from surface to 800 hPa) for Europe, ETR and Siberia depending on region is 1.5–2.4 Tg in warm period (1 April – 30 September) and 1.3–2.2 Tg in cold period (1 October - 31 March). Ozone production in chemical processes with a high degree of accuracy (about 99%) is balanced by total atmospheric transport, while absolute variations in O<sub>3 </sub>total mass do not exceed 0.5 Tg/year in Europe and 0.4 Tg/year in Siberia.<br>This work was supported by the Russian Foundation for Basic Research under grant 18-35-20031.</p>


2014 ◽  
Vol 14 (1) ◽  
pp. 115-132 ◽  
Author(s):  
P. Zanis ◽  
P. Hadjinicolaou ◽  
A. Pozzer ◽  
E. Tyrlis ◽  
S. Dafka ◽  
...  

Abstract. Observations show that the Mediterranean troposphere is characterized by a marked enhancement in summertime ozone, with a maximum over the eastern Mediterranean. This has been linked to enhanced photochemical ozone production and subsidence under cloud-free anticyclonic conditions. The eastern Mediterranean is among the regions with the highest levels of background tropospheric ozone worldwide. A 12 yr climatological analysis (1998–2009) of free-tropospheric ozone was carried out over the region based on the ECMWF (European Centre for Medium-Range Weather Forecasts) ERA-Interim reanalysis data and simulations with the EMAC (ECHAM5–MESSy) atmospheric chemistry–climate model. EMAC is nudged towards the ECMWF analysis data and includes a stratospheric ozone tracer. A characteristic summertime pool with high ozone concentrations is found in the middle troposphere over the eastern Mediterranean–Middle East (EMME) in the ERA-Interim ozone data, Tropospheric Emission Spectrometer (TES) satellite ozone data and simulations with EMAC. The enhanced ozone over the EMME during summer is a robust feature, extending down to lower free-tropospheric levels. The investigation of ozone in relation to potential vorticity and water vapour and the stratospheric ozone tracer indicates that the dominant mechanism causing the free-tropospheric ozone pool is the downward transport from the upper troposphere and lower stratosphere, in association with the enhanced subsidence and the limited horizontal divergence observed over the region. The implications of these high free-tropospheric ozone levels on the seasonal cycle of near-surface ozone over the Mediterranean are discussed.


Atmosphere ◽  
2020 ◽  
Vol 11 (2) ◽  
pp. 206
Author(s):  
Jieun Wie ◽  
Hyo-Jin Park ◽  
Hyomee Lee ◽  
Byung-Kwon Moon

This study examined the variability of near-surface (850 hPa) ozone during summer in East Asia using simulations from 12 models participating in the Chemistry–Climate Model Initiative (CCMI). The empirical orthogonal function (EOF) analysis of non-detrended ozone shows that the first (second) EOF mode is characterized by a monopole (dipole) structure that describe 83.3% (7.1%) of total variance. The corresponding the first principle component (PC1) time series exhibits a gradually increasing trend due to the rising anthropogenic emission, whereas PC2 shows interannual variation. To understand the drivers of this interannual variability, the detrended ozone is also analyzed. The two leading EOF patterns of detrended ozone, EOF1 and EOF2, explain 37.0% and 29.2% of the total variance, respectively. The regression results indicate that the positive ozone anomaly in East Asia associated with EOF1 is caused by the combination of net ozone production and transport from the upper atmosphere. In contrast, EOF2 is associated with the weakened western Pacific subtropical high during the La Niña decaying summer, which tends to decrease monsoon precipitation, thus increasing ozone concentration in China. Our results suggest that the El Niño-Southern Oscillation (ENSO) plays a key role in driving interannual variability in tropospheric ozone in East Asia.


2021 ◽  
Vol 258 ◽  
pp. 105653
Author(s):  
Anshika ◽  
Ravi Kumar Kunchala ◽  
Raju Attada ◽  
Ramesh K. Vellore ◽  
Vijay K. Soni ◽  
...  

2021 ◽  
Vol 13 (10) ◽  
pp. 1958
Author(s):  
Shelly Elbaz ◽  
Efrat Sheffer ◽  
Itamar M. Lensky ◽  
Noam Levin

Discriminating between woody plant species using a single image is not straightforward due to similarity in their spectral signatures, and limitations in the spatial resolution of many sensors. Seasonal changes in vegetation indices can potentially improve vegetation mapping; however, for mapping at the individual species level, very high spatial resolution is needed. In this study we examined the ability of the Israel/French satellite of VENμS and other sensors with higher spatial resolutions, for identifying woody Mediterranean species, based on the seasonal patterns of vegetation indices (VIs). For the study area, we chose a site with natural and highly heterogeneous vegetation in the Judean Mountains (Israel), which well represents the Mediterranean maquis vegetation of the region. We used three sensors from which the indices were derived: a consumer-grade ground-based camera (weekly images at VIS-NIR; six VIs; 547 individual plants), UAV imagery (11 images, five bands, seven VIs) resampled to 14, 30, 125, and 500 cm to simulate the spatial resolutions available from some satellites, and VENμS Level 1 product (with a nominal spatial resolution of 5.3 m at nadir; seven VIs; 1551 individual plants). The various sensors described seasonal changes in the species’ VIs at different levels of success. Strong correlations between the near-surface sensors for a given VI and species mostly persisted for all spatial resolutions ≤125 cm. The UAV ExG index presented high correlations with the ground camera data in most species (pixel size ≤125 cm; 9 of 12 species with R ≥ 0.85; p < 0.001), and high classification accuracies (pixel size ≤30 cm; 8 species with >70%), demonstrating the possibility for detailed species mapping from space. The seasonal dynamics of the species obtained from VENμS demonstrated the dominant role of ephemeral herbaceous vegetation on the signal recorded by the sensor. The low variance between the species as observed from VENμS may be explained by its coarse spatial resolution (effective ground spatial resolution of 7.5) and its non-nadir viewing angle (29.7°) over the study area. However, considering the challenging characteristics of the research site, it may be that using a VENμS type sensor (with a spatial resolution of ~1 m) from a nadir point of view and in more homogeneous and dense areas would allow for detailed mapping of Mediterranean species based on their seasonality.


2009 ◽  
Vol 9 (11) ◽  
pp. 3731-3743 ◽  
Author(s):  
M. Mena-Carrasco ◽  
G. R. Carmichael ◽  
J. E. Campbell ◽  
D. Zimmerman ◽  
Y. Tang ◽  
...  

Abstract. The impact of Mexico City (MCMA) emissions is examined by studying its effects on air quality, photochemistry, and on ozone production regimes by combining model products and aircraft observations from the MILAGRO experiment during March 2006. The modeled influence of MCMA emissions to enhancements in surface level NOx, CO, and O3 concentrations (10–30% increase) are confined to distances <200 km, near surface. However, the extent of the influence is significantly larger at higher altitudes. Broader MCMA impacts (some 900 km Northeast of the city) are shown for specific outflow conditions in which enhanced ozone, NOy, and MTBE mixing ratios over the Gulf of Mexico are linked to MCMA by source tagged tracers and sensitivity runs. This study shows that the "footprint" of MCMA on average is fairly local, with exception to reactive nitrogen, which can be transported long range in the form of PAN, acting as a reservoir and source of NOx with important regional ozone formation implications. The simulated effect of MCMA emissions of anthropogenic aerosol on photochemistry showed a maximum regional decrease of 40% in J[NO2→NO+O], and resulting in the reduction of ozone production by 5–10%. Observed ozone production efficiencies are evaluated as a function of distance from MCMA, and by modeled influence from MCMA. These tend to be much lower closer to MCMA, or in those points where modeled contribution from MCMA is large. This research shows that MCMA emissions do effect on regional air quality and photochemistry, both contributing large amounts of ozone and its precursors, but with caveat that aerosol concentrations hinder formation of ozone to its potential due to its reduction in photolysis rates.


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.


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