scholarly journals Influence of the wintertime North Atlantic Oscillation on European tropospheric composition: an observational and modelling study

2018 ◽  
Vol 18 (11) ◽  
pp. 8389-8408 ◽  
Author(s):  
Richard J. Pope ◽  
Martyn P. Chipperfield ◽  
Stephen R. Arnold ◽  
Norbert Glatthor ◽  
Wuhu Feng ◽  
...  

Abstract. We have used satellite observations and a simulation from the TOMCAT chemistry transport model (CTM) to investigate the influence of the well-known wintertime North Atlantic Oscillation (NAO) on European tropospheric composition. Under the positive phase of the NAO (NAO-high), strong westerlies tend to enhance transport of European pollution (e.g. nitrogen oxides, NOx; carbon monoxide, CO) away from anthropogenic source regions. In contrast, during the negative phase of the NAO (NAO-low), more stable meteorological conditions lead to a build-up of pollutants over these regions relative to the wintertime average pollution levels. However, the secondary pollutant ozone shows the opposite signal of larger values during NAO-high. NAO-high introduces Atlantic ozone-enriched air into Europe, while under NAO-low westerly transport of ozone is reduced, yielding lower values over Europe. Furthermore, ozone concentrations are also decreased by chemical loss through the reaction with accumulated primary pollutants such as nitric oxide (NO) in NAO-low. Peroxyacetyl nitrate (PAN) in the upper troposphere–lower stratosphere (UTLS) peaks over Iceland and southern Greenland in NAO-low, between 200 and 100 hPa, consistent with the trapping by an anticyclone at this altitude. Model simulations show that enhanced PAN over Iceland and southern Greenland in NAO-low is associated with vertical transport of polluted air from the mid-troposphere into the UTLS. Overall, this work shows that NAO circulation patterns are an important governing factor for European wintertime composition and air pollution.

2017 ◽  
Author(s):  
Richard J. Pope ◽  
Martyn P. Chipperfield ◽  
Stephen R. Arnold ◽  
Norbert Glatthor ◽  
Wuhu Feng ◽  
...  

Abstract. We have used satellite observations and a simulation from the TOMCAT chemistry transport model (CTM) to investigate the influence of the well-known winter-time North Atlantic Oscillation (NAO) on European tropospheric composition. Under the positive phase of the NAO (NAO+), strong westerlies tend to enhance transport of European pollution (e.g. nitrogen oxides, NOx, carbon monoxide, CO) away from anthropogenic source regions. In contrast, during the negative phase of the NAO (NAO−), more stable meteorological conditions lead to a build up of pollutants over these regions, relative to the winter-time average pollution levels. However, the secondary pollutant ozone shows the opposite signal of larger values during NAO+. NAO+ introduces Atlantic ozone-enriched air into Europe while under NAO− westerly transport of ozone is reduced yielding lower values over Europe. Furthermore, ozone concentrations are also decreased by chemical loss through the reaction with accumulated primary pollutants such as nitric oxide (NO) in NAO−. Peroxyacetyl nitrate (PAN), in the upper troposphere-lower stratosphere (UTLS) peaks over Iceland/Southern Greenland in NAO−, between 200–100 hPa, consistent with the trapping by an anticyclone at this altitude. Model simulations show enhanced PAN over Iceland/Southern Greenland in NAO− is associated with vertical transport of polluted air from the troposphere into the UTLS. Overall, this work shows that NAO circulation patterns are an important governing factor for European winter-time composition and air pollution.


2010 ◽  
Vol 10 (3) ◽  
pp. 1345-1359 ◽  
Author(s):  
G. G. Pfister ◽  
L. K. Emmons ◽  
D. P. Edwards ◽  
A. Arellano ◽  
T. Campos ◽  
...  

Abstract. We analyze the transport of pollution across the Pacific during the NASA INTEX-B (Intercontinental Chemical Transport Experiment Part B) campaign in spring 2006 and examine how this year compares to the time period for 2000 through 2006. In addition to aircraft measurements of carbon monoxide (CO) collected during INTEX-B, we include in this study multi-year satellite retrievals of CO from the Measurements of Pollution in the Troposphere (MOPITT) instrument and simulations from the chemistry transport model MOZART-4. Model tracers are used to examine the contributions of different source regions and source types to pollution levels over the Pacific. Additional modeling studies are performed to separate the impacts of inter-annual variability in meteorology and dynamics from changes in source strength. Interannual variability in the tropospheric CO burden over the Pacific and the US as estimated from the MOPITT data range up to 7% and a somewhat smaller estimate (5%) is derived from the model. When keeping the emissions in the model constant between years, the year-to-year changes are reduced (2%), but show that in addition to changes in emissions, variable meteorological conditions also impact transpacific pollution transport. We estimate that about 1/3 of the variability in the tropospheric CO loading over the contiguous US is explained by changes in emissions and about 2/3 by changes in meteorology and transport. Biomass burning sources are found to be a larger driver for inter-annual variability in the CO loading compared to fossil and biofuel sources or photochemical CO production even though their absolute contributions are smaller. Source contribution analysis shows that the aircraft sampling during INTEX-B was fairly representative of the larger scale region, but with a slight bias towards higher influence from Asian contributions.


2009 ◽  
Vol 9 (4) ◽  
pp. 17817-17849 ◽  
Author(s):  
G. G. Pfister ◽  
L. K. Emmons ◽  
D. P. Edwards ◽  
A. Arellano ◽  
G. Sachse ◽  
...  

Abstract. We analyze the transport of pollution across the Pacific during the NASA INTEX-B (Intercontinental Chemical Transport Experiment Part B) campaign in spring 2006 and examine how this year compares to the time period for 2000 through 2006. In addition to aircraft measurements of carbon monoxide (CO) collected during INTEX-B, we include in this study multi-year satellite retrievals of CO from the Measurements of Pollution in the Troposphere (MOPITT) instrument and simulations from the chemistry transport model MOZART-4. Model tracers are used to examine the contributions of different source regions and source types to pollution levels over the Pacific. Additional modeling studies are performed to separate the impacts of inter-annual variability in meteorology and dynamics from changes in source strength. Interannual variability in the tropospheric CO burden over the Pacific and the US as estimated from the MOPITT data range up to 7% and a somewhat smaller estimate (5%) is derived from the model. When keeping the emissions in the model constant between years, the year-to-year changes are reduced to (2%), but show that in addition to changes in emissions, variable meteorological conditions also impact transpacific pollution transport. We estimate that about 1/3 of the variability in the tropospheric CO loading over the contiguous US is explained by changes in emissions and about 2/3 by changes in meteorology and transport. Biomass burning sources are found to be a larger driver for inter-annual variability in the CO loading compared to fossil and biofuel sources or photochemical CO production even though their absolute contributions are smaller. Source contribution analysis shows that the aircraft sampling during INTEX-B was fairly representative of the larger scale region, but with a slight bias towards higher influence from Asian contributions.


2021 ◽  
Author(s):  
Pedro Jiménez-Guerrero ◽  
Nuno Ratola

AbstractThe atmospheric concentration of persistent organic pollutants (and of polycyclic aromatic hydrocarbons, PAHs, in particular) is closely related to climate change and climatic fluctuations, which are likely to influence contaminant’s transport pathways and transfer processes. Predicting how climate variability alters PAHs concentrations in the atmosphere still poses an exceptional challenge. In this sense, the main objective of this contribution is to assess the relationship between the North Atlantic Oscillation (NAO) index and the mean concentration of benzo[a]pyrene (BaP, the most studied PAH congener) in a domain covering Europe, with an emphasis on the effect of regional-scale processes. A numerical simulation for a present climate period of 30 years was performed using a regional chemistry transport model with a 25 km spatial resolution (horizontal), higher than those commonly applied. The results show an important seasonal behaviour, with a remarkable spatial pattern of difference between the north and the south of the domain. In winter, higher BaP ground levels are found during the NAO+ phase for the Mediterranean basin, while the spatial pattern of this feature (higher BaP levels during NAO+ phases) moves northwards in summer. These results show deviations up to and sometimes over 100% in the BaP mean concentrations, but statistically significant signals (p<0.1) of lower changes (20–40% variations in the signal) are found for the north of the domain in winter and for the south in summer.


2015 ◽  
Vol 15 (23) ◽  
pp. 33897-33929 ◽  
Author(s):  
H. Lee ◽  
O. V. Kalashnikova ◽  
K. Suzuki ◽  
A. Braverman ◽  
M. J. Garay ◽  
...  

Abstract. The Multi-angle Imaging SpectroRadiometer (MISR) Joint Aerosol (JOINT_AS) Level 3 product provides a global, descriptive summary of MISR Level 2 aerosol optical depth (AOD) and aerosol type information for each month between March 2000 and the present. Using Version 1 of JOINT_AS, which is based on the operational (Version 22) MISR Level 2 aerosol product, this study analyzes, for the first time, characteristics of observed and simulated distributions of AOD for three broad classes of aerosols: non-absorbing, absorbing, and non-spherical – near or downwind of their major source regions. The statistical moments (means, standard deviations, and skewnesses) and distributions of AOD by components derived from the JOINT_AS are compared with results from the SPectral RadIatioN-TrAnSport (SPRINTARS) model, a chemistry transport model (CTM) with very high spatial and temporal resolution. Overall, the AOD distributions of combined MISR aerosol types show good agreement with those from SPRINTARS. Marginal distributions of AOD for each aerosol type in both MISR and SPRINTARS show considerable high positive skewness, which indicates the importance of including extreme AOD events when comparing satellite retrievals with models. The MISR JOINT_AS product will greatly facilitate comparisons between satellite observations and model simulations of aerosols by type.


2009 ◽  
Vol 26 (6) ◽  
pp. 1135-1143 ◽  
Author(s):  
Maria Raffaella Vuolo ◽  
Laurent Menut ◽  
Hélène Chepfer

Abstract A sensitivity study is performed with the CHIMERE-DUST chemistry transport model in order to evaluate the modeled mineral dust spread due to the horizontal transport scheme accuracy. Three different schemes are implemented in the model: the simple first-order UPWIND scheme, the second-order Van Leer scheme, and the third-order parabolic piecewise method (PPM) scheme. The results showed that a large part of the uncertainty in dust modeling may be due to the transport scheme only. Compared to the PPM scheme, it is shown that, over a large domain encompassing western Africa and the North Atlantic, a significant increase in the dust plume extension is locally diagnosed (+25% with Van Leer and +48% with UPWIND) and linked to a decrease in the dust maxima (−17% with Van Leer and −32% with UPWIND) to PPM. Far from the sources, hourly surface concentration differences may be up to 30 μg m−3 in Europe, highlighting the high uncertainty of dust modeling for air quality use.


2017 ◽  
Author(s):  
Lars Norin ◽  
Abhay Devasthale ◽  
Tristan S. L'Ecuyer

Abstract. For a high latitude country like Sweden snowfall is an important contributor to the regional water cycle. Furthermore, snowfall impacts surface properties, affects atmospheric thermodynamics, has implications for traffic and logistics management, disaster preparedness, and also impacts climate through changes in surface albedo and turbulent heat fluxes. For Sweden it has been shown that large-scale atmospheric circulation patterns, or weather states, are important for precipitation variability. Although the link between atmospheric circulation patterns and precipitation has been investigated for rainfall there are no studied focused on the sensitivity of snowfall to weather states over Sweden. In this work we investigate the response of snowfall to eight selected weather states. These weather states consist of four dominant wind directions together with cyclonic and anti-cyclonic circulation patterns and enhanced positive and negative phases of the North Atlantic oscillation. The presented analysis is based on multiple data sources, such as ground-based radar measurements, satellite observations, spatially-interpolated in situ observations, and reanalysis data. The data from these sources converge to underline the sensitivity of falling snow over Sweden to the different weather states. In this paper we examine both average snowfall intensities and snowfall accumulations associated with the different weather states. It is shown that even though the heaviest snowfall intensities occur during conditions with winds from the southwest, the largest contribution to snowfall accumulation arrives from winds from the southeast. Large differences in snowfall due to variations in the North Atlantic oscillation are shown as well as a strong effect of cyclonic and anti-cyclonic circulation patterns. Satellite observations are used to reveal the vertical structures of snowfall during the different weather states.


Author(s):  
C Giannakopoulos ◽  
P Good ◽  
K S Law ◽  
D E Shallcross ◽  
K-Y Wang

A three-dimensional chemistry-transport model has been used to assess the impacts of aircraft traffic in the upper troposphere. Aircraft engines emit NOx, which has the potential to perturb the chemical composition at the flight altitude paths, i.e. at a 10–12 km height for subsonic flights. The model used includes a comprehensive chemistry scheme, so perturbations to other species apart from NOx could also be examined. More specifically, the model showed that the monthly mean increase for NOx due to aircraft is around 60 pptv (parts per trillion volume (30 per cent increase) and for HNO3 it is 100 pptv (30 per cent increase). Consequently, O3 is enhanced by 2500 pptv (5 per cent increase) due to aircraft traffic. To assess the regional and temporal variations in the perturbations, a time series analysis above a central European grid cell located at 47 °N 18 °E has also been performed. The analysis has indicated that the local perturbations can be much larger than the monthly mean values and can reach 200 pptv for NOx, 150 pptv for HNO3 and 5000 pptv for O3.


2005 ◽  
Vol 5 (7) ◽  
pp. 1815-1834 ◽  
Author(s):  
L. J. Labrador ◽  
R. von Kuhlmann ◽  
M. G. Lawrence

Abstract. The impact of different assumptions concerning the source magnitude as well as the vertical placement of lightning-produced nitrogen oxides is studied using the global chemistry transport model MATCH-MPIC. The responses of NOx, O3, OH, HNO3 and peroxyacetyl-nitrate (PAN) are investigated. A marked sensitivity to both parameters is found. NOx burdens globally can be enhanced by up to 100% depending on the vertical placement and source magnitude strength. In all cases, the largest enhancements occur in the tropical upper troposphere, where lifetimes of most trace gases are longer and where they thus become more susceptible to long-range transport by large-scale circulation patterns. Comparison with observations indicate that 0 and 20 Tg(N)/yr production rates of NOx from lightning are too low and too high, respectively. However, no single intermediate production rate or vertical distribution can be singled out as best fitting the observations, due to the large scatter in the datasets. This underscores the need for further measurement campaigns in key regions, such as the tropical continents.


2017 ◽  
Author(s):  
Heiko Bozem ◽  
Tim M. Butler ◽  
Mark G. Lawrence ◽  
Hartwig Harder ◽  
Monica Martinez ◽  
...  

Abstract. Ozone (O3) is an important atmospheric oxidant, a greenhouse gas, and a hazard to human health and agriculture. Here we describe airborne in-situ measurements and model simulations of O3 and its precursors during tropical and extratropical field campaigns over South America and Europe, respectively. Using the measurements, net ozone formation/destruction tendencies are calculated and compared to 3D chemistry-transport model simulations. In general, observation-based net ozone tendencies are positive in the continental boundary layer and the upper troposphere at altitudes above ~ 6 km in both environments. On the other hand, in the marine boundary layer and the middle troposphere, from the top of the boundary layer to about 6–8 km altitude, net O3 destruction prevails. The ozone tendencies are controlled by ambient concentrations of nitrogen oxides (NOx). In regions with net ozone destruction the available NOx is below the threshold value at which production and destruction of O3 balance. While threshold NO values increase with altitude, in the upper troposphere NOx concentrations are generally higher, probably due to the integral effect of convective precursor transport from the boundary layer and NOx produced by lightning. Two case studies indicate that in fresh convective outflow of electrified thunderstorms net ozone production is enhanced by a factor 5–6 compared to the undisturbed upper tropospheric background. The chemistry-transport model MATCH-MPIC generally reproduces the pattern of observation-based net ozone tendencies, but mostly underestimates the magnitude of the net tendency (for both net ozone production and destruction).


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