MOdèle De Chimie Atmosphérique À Grande Echelle Research Articles

Interpol-IAGOS: a new method for assessing long-term chemistry–climate simulations in the UTLS based on IAGOS data, and its application to the MOCAGE CCMI REF-C1SD simulation

Abstract. A wide variety of observation data sets are used to assess long-term simulations provided by chemistry–climate models (CCMs) and chemistry-transport models (CTMs). However, the upper troposphere–lower stratosphere (UTLS) has hardly been assessed in these modelling exercises yet. Observations performed in the framework of IAGOS (In-service Aircraft for a Global Observing System) combine the advantages of in situ airborne measurements in the UTLS with an almost-global-scale sampling, a ∼20-year monitoring period and a high frequency. Even though a few model assessments have been made using the IAGOS database, none of them took advantage of the dense and high-resolution cruise data in their whole ensemble yet. The present study proposes a method to compare this large IAGOS data set to long-term simulations used for chemistry–climate studies. As a first application, the REF-C1SD reference simulation generated by the MOCAGE (MOdèle de Chimie Atmosphérique à Grande Echelle) CTM in the framework of Chemistry-Climate Model Initiative (CCMI) phase I has been evaluated during the 1994–2013 period for ozone (O3) and the 2002–2013 period for carbon monoxide (CO). The concept of the new comparison software proposed here (so-called Interpol-IAGOS) is to project all IAGOS data onto the 3-D grid of the model with a monthly resolution, since generally the 3-D outputs provided by chemistry–climate models for multi-model comparisons on multi-decadal timescales are archived as monthly means. This provides a new IAGOS data set (IAGOS-DM) mapped onto the model's grid and time resolution. To get a model data set consistent with IAGOS-DM for the comparison, a subset of the model's outputs is created (MOCAGE-M) by applying a mask that retains only the model data at the available IAGOS-DM grid points. Climatologies are derived from the IAGOS-DM product, and good correlations are reported between with the MOCAGE-M spatial distributions. As an attempt to analyse MOCAGE-M behaviour in the upper troposphere (UT) and the lower stratosphere (LS) separately, UT and LS data in IAGOS-DM were sorted according to potential vorticity. From this, we derived O3 and CO seasonal cycles in eight regions well sampled by IAGOS flights in the northern midlatitudes. They are remarkably well reproduced by the model for lower-stratospheric O3 and also good for upper-tropospheric CO. Along this model evaluation, we also assess the differences caused by the use of a weighting function in the method when projecting the IAGOS data onto the model grid compared to the scores derived in a simplified way. We conclude that the data projection onto the model's grid allows us to filter out biases arising from either spatial or temporal resolution, and the use of a weighting function yields different results, here by enhancing the assessment scores. Beyond the MOCAGE REF-C1SD evaluation presented in this paper, the method could be used by CCMI models for individual assessments in the UTLS and for model intercomparisons with respect to the IAGOS data set.

Estimation of the error covariance matrix for IASI radiances and its impact on the assimilation of ozone in a chemistry transport model

Abstract. In atmospheric chemistry retrievals and data assimilation systems, observation errors associated with satellite radiances are chosen empirically and generally treated as uncorrelated. In this work, we estimate inter-channel error covariances for the Infrared Atmospheric Sounding Interferometer (IASI) and evaluate their impact on ozone assimilation with the chemistry transport model MOCAGE (Modèle de Chimie Atmosphérique à Grande Echelle). The method used to calculate observation errors is a diagnostic based on the observation and analysis residual statistics already adopted in many numerical weather prediction centres. We used a subset of 280 channels covering the spectral range between 980 and 1100 cm−1 to estimate the observation-error covariance matrix. This spectral range includes ozone-sensitive and atmospheric window channels. We computed hourly 3D-Var analyses and compared the resulting O3 fields against ozonesondes and the measurements provided by the Microwave Limb Sounder (MLS) and by the Ozone Monitoring Instrument (OMI). The results show significant differences between using the estimated error covariance matrix with respect to the empirical diagonal matrix employed in previous studies. The validation of the analyses against independent data reports a significant improvement, especially in the tropical stratosphere. The computational cost has also been reduced when the estimated covariance matrix is employed in the assimilation system, by reducing the number of iterations needed for the minimizer to converge.

Aerosol data assimilation in the MOCAGE chemical transport model during the TRAQA/ChArMEx campaign: lidar observations

Abstract. This paper presents the first results about the assimilation of CALIOP (Cloud-Aerosol Lidar with Orthogonal Polarization) extinction coefficient measurements onboard the CALIPSO (Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations) satellite in the MOCAGE (MOdèle de Chimie Atmosphérique à Grande Echelle) chemistry transport model of Météo-France. This assimilation module is an extension of the aerosol optical depth (AOD) assimilation system already presented by Sič et al. (2016). We focus on the period of the TRAQA (TRAnsport à longue distance et Qualité de l’Air dans le bassin méditerranéen) field campaign that took place during summer 2012. This period offers the opportunity to have access to a large set of aerosol observations from instrumented aircraft, balloons, satellite and ground-based stations. We evaluate the added value of CALIOP assimilation with respect to the model free run by comparing both fields to independent observations issued from the TRAQA field campaign. In this study we focus on the desert dust outbreak which happened during late June 2012 over the Mediterranean Basin (MB) during the TRAQA campaign. The comparison with the AERONET (Aerosol Robotic Network) AOD measurements shows that the assimilation of CALIOP lidar observations improves the statistics compared to the model free run. The correlation between AERONET and the model (assimilation) is 0.682 (0.753); the bias and the root mean square error (RMSE), due to CALIOP assimilation, are reduced from −0.063 to 0.048 and from 0.183 to 0.148, respectively. Compared to MODIS (Moderate-resolution Imaging Spectroradiometer) AOD observations, the model free run shows an underestimation of the AOD values, whereas the CALIOP assimilation corrects this underestimation and shows a quantitative good improvement in terms of AOD maps over the MB. The correlation between MODIS and the model (assimilation) during the dust outbreak is 0.47 (0.52), whereas the bias is −0.18 (−0.02) and the RMSE is 0.36 (0.30). The comparison of in situ aircraft and balloon measurements to both modelled and assimilated outputs shows that the CALIOP lidar assimilation highly improves the model aerosol field. The evaluation with the LOAC (Light Optical Particle Counter) measurements indicates that the aerosol vertical profiles are well simulated by the direct model but with a general underestimation of the aerosol number concentration, especially in the altitude range 2–5 km. The CALIOP assimilation improves these results by a factor of 2.5 to 5. Analysis of the vertical distribution of the desert aerosol concentration shows that the aerosol dust transport event is well captured by the model but with an underestimated intensity. The assimilation of CALIOP observations allows the improvement of the geographical representation of the event within the model as well as its intensity by a factor of 2 in the altitude range 1–5 km.

Benefit of ozone observations from Sentinel-5P and future Sentinel-4 missions on tropospheric composition

Abstract. We present an observing simulated system experiment (OSSE) dedicated to evaluate the potential added value from the Sentinel-4 and the Sentinel-5P observations on tropospheric ozone composition. For this purpose, the ozone data of Sentinel-4 (Ultraviolet Visible Near-infrared) and Sentinel-5P (TROPOspheric Monitoring Instrument) on board a geostationary (GEO) and a low-Earth-orbit (LEO) platform, respectively, have been simulated using the DISAMAR inversion package for the summer 2003. To ensure the robustness of the results, the OSSE has been configured with conservative assumptions. We simulate the reality by combining two chemistry transport models (CTMs): the LOng Term Ozone Simulation – EURopean Operational Smog (LOTOS-EUROS) and the Transport Model version 5 (TM5). The assimilation system is based on a different CTM, the MOdèle de Chimie Atmosphérique à Grande Echelle (MOCAGE), combined with the 3-D variational technique. The background error covariance matrix does not evolve in time and its variance is proportional to the field values. The simulated data are formed of six eigenvectors to minimize the size of the dataset by removing the noise-dominated part of the observations. The results show that the satellite data clearly bring direct added value around 200 hPa for the whole assimilation period and for the whole European domain, while a likely indirect added value is identified but not for the whole period and domain at 500 hPa, and to a lower extent at 700 hPa. In addition, the ozone added value from Sentinel-5P (LEO) appears close to that from Sentinel-4 (GEO) in the free troposphere (200–500 hPa) in our OSSE. The outcome of our study is a result of the OSSE design and the choice within each of the components of the system.

Assimilation of IASI Ozone‐Sensitive Channels in Preparation for an Enhanced Coupling Between Numerical Weather Prediction and Chemistry Transport Models

AbstractIn this study, IASI ozone‐sensitive channels have been assimilated in 1D‐Var data assimilation combined with realistic ozone background coming from a MOCAGE (Modèle de Chimie Atmosphérique à Grande Echelle) Chemistry Transport Model (CTM) as a first stage of coupling between Numerical Weather Prediction (NWP) and MOCAGE CTM at Météo‐France for global model ARPEGE (Action de Recherche Petite Echelle Grande Echelle). To evaluate the impact of ozone‐sensitive channels on analyses, databases of 161 temperatures, humidity, and ozone radiosondes across the globe during a 1‐year period have been considered. Ozone forecast from MOCAGE CTM was evaluated with radiosondes and used as input for the Radiative Transfer Model (RTM) RTTOV. Statistics of IASI observations minus simulations show that the use of ozone from MOCAGE CTM allows to better simulate IASI ozone‐sensitive channels. The Desroziers method is used to diagnose observation error covariance matrix and estimate realistic ozone observation standard errors taking into account cross‐correlations between IASI channels. The background error covariance matrix for ozone is estimated using radiosondes. A control run assimilating 123 IASI operational channels is compared to an experiment which assimilates, in addition, 15 IASI ozone‐sensitive channels. Results show potential benefits of IASI ozone‐sensitive channels combined with realistic ozone from MOCAGE CTM to improve temperature, humidity and ozone analyses simultaneously. This work is an encouraging first step for the enhancing of the coupling between the global model ARPEGE and MOCAGE CTM.

Multi-year assimilation of IASI and MLS ozone retrievals: variability of tropospheric ozone over the tropics in response to ENSO

Abstract. The Infrared Atmospheric Sounder Instrument (IASI) allows global coverage with very high spatial resolution and its measurements are promising for long-term ozone monitoring. In this study, Microwave Limb Sounder (MLS) O3 profiles and IASI O3 partial columns (1013.25–345 hPa) are assimilated in a chemistry transport model to produce 6-hourly analyses of tropospheric ozone for 6 years (2008–2013). We have compared and evaluated the IASI-MLS analysis and the MLS analysis to assess the added value of IASI measurements. The global chemical transport model MOCAGE (MOdèle de Chimie Atmosphérique à Grande Echelle) has been used with a linear ozone chemistry scheme and meteorological forcing fields from ERA-Interim (ECMWF global reanalysis) with a horizontal resolution of 2° × 2° and 60 vertical levels. The MLS and IASI O3 retrievals have been assimilated with a 4-D variational algorithm to constrain stratospheric and tropospheric ozone respectively. The ozone analyses are validated against ozone soundings and tropospheric column ozone (TCO) from the OMI-MLS residual method. In addition, an Ozone ENSO Index (OEI) is computed from the analysis to validate the TCO variability during the ENSO events. We show that the assimilation of IASI reproduces the variability of tropospheric ozone well during the period under study. The variability deduced from the IASI-MLS analysis and the OMI-MLS measurements are similar for the period of study. The IASI-MLS analysis can reproduce the extreme oscillation of tropospheric ozone caused by ENSO events over the tropical Pacific Ocean, although a correction is required to reduce a constant bias present in the IASI-MLS analysis.

Aerosol data assimilation in the chemical transport model MOCAGE during the TRAQA/ChArMEx campaign: aerosol optical depth

Abstract. In this study, we describe the development of the aerosol optical depth (AOD) assimilation module in the chemistry transport model (CTM) MOCAGE (Modèle de Chimie Atmosphérique à Grande Echelle). Our goal is to assimilate the spatially averaged 2-D column AOD data from the National Aeronautics and Space Administration (NASA) Moderate-resolution Imaging Spectroradiometer (MODIS) instrument, and to estimate improvements in a 3-D CTM assimilation run compared to a direct model run. Our assimilation system uses 3-D-FGAT (first guess at appropriate time) as an assimilation method and the total 3-D aerosol concentration as a control variable. In order to have an extensive validation dataset, we carried out our experiment in the northern summer of 2012 when the pre-ChArMEx (CHemistry and AeRosol MEditerranean EXperiment) field campaign TRAQA (TRAnsport à longue distance et Qualité de l'Air dans le bassin méditerranéen) took place in the western Mediterranean basin. The assimilated model run is evaluated independently against a range of aerosol properties (2-D and 3-D) measured by in situ instruments (the TRAQA size-resolved balloon and aircraft measurements), the satellite Spinning Enhanced Visible and InfraRed Imager (SEVIRI) instrument and ground-based instruments from the Aerosol Robotic Network (AERONET) network. The evaluation demonstrates that the AOD assimilation greatly improves aerosol representation in the model. For example, the comparison of the direct and the assimilated model run with AERONET data shows that the assimilation increased the correlation (from 0.74 to 0.88), and reduced the bias (from 0.050 to 0.006) and the root mean square error in the AOD (from 0.12 to 0.07). When compared to the 3-D concentration data obtained by the in situ aircraft and balloon measurements, the assimilation consistently improves the model output. The best results as expected occur when the shape of the vertical profile is correctly simulated by the direct model. We also examine how the assimilation can influence the modelled aerosol vertical distribution. The results show that a 2-D continuous AOD assimilation can improve the 3-D vertical profile, as a result of differential horizontal transport of aerosols in the model.

Modelling of primary aerosols in the chemical transport model MOCAGE: development and evaluation of aerosol physical parameterizations

Abstract. This paper deals with recent improvements to the global chemical transport model of Météo-France MOCAGE (Modèle de Chimie Atmosphérique à Grande Echelle) that consists of updates to different aerosol parameterizations. MOCAGE only contains primary aerosol species: desert dust, sea salt, black carbon, organic carbon, and also volcanic ash in the case of large volcanic eruptions. We introduced important changes to the aerosol parameterization concerning emissions, wet deposition and sedimentation. For the emissions, size distribution and wind calculations are modified for desert dust aerosols, and a surface sea temperature dependant source function is introduced for sea salt aerosols. Wet deposition is modified toward a more physically realistic representation by introducing re-evaporation of falling rain and snowfall scavenging and by changing the in-cloud scavenging scheme along with calculations of precipitation cloud cover and rain properties. The sedimentation scheme update includes changes regarding the stability and viscosity calculations. Independent data from satellites (MODIS, SEVIRI), the ground (AERONET, EMEP), and a model inter-comparison project (AeroCom) are compared with MOCAGE simulations and show that the introduced changes brought a significant improvement on aerosol representation, properties and global distribution. Emitted quantities of desert dust and sea salt, as well their lifetimes, moved closer towards values of AeroCom estimates and the multi-model average. When comparing the model simulations with MODIS aerosol optical depth (AOD) observations over the oceans, the updated model configuration shows a decrease in the modified normalized mean bias (MNMB; from 0.42 to 0.10) and a better correlation (from 0.06 to 0.32) in terms of the geographical distribution and the temporal variability. The updates corrected a strong positive MNMB in the sea salt representation at high latitudes (from 0.65 to 0.16), and a negative MNMB in the desert dust representation in the African dust outflow region (from −1.01 to −0.22). The updates in sedimentation produced a modest difference; the MNMB with MODIS data from 0.10 in the updated configuration went to 0.11 in the updated configuration only without the sedimentation updates. Yet, the updates in the emissions and the wet deposition made a stronger impact on the results; the MNMB was 0.27 and 0.21 in updated configurations only without emission, and only without wet deposition updates, respectively. Also, the lifetime, the extent, and the strength of the episodic aerosol events are better reproduced in the updated configuration. The wet deposition processes and the differences between the various configurations that were tested greatly influence the representation of the episodic events. However, wet deposition is not a continuous process; it has a local and episodic signature and its representation depends strongly on the precipitation regime in the model.

Validation of nine years of MOPITT V5 NIR using MOZAIC/IAGOS measurements: biases and long-term stability

Abstract. Validation results from a comparison between Measurement Of Pollution In The Troposphere (MOPITT) V5 Near InfraRed (NIR) carbon monoxide (CO) total column measurements and Measurement of Ozone and Water Vapour on Airbus in-service Aircraft (MOZAIC)/In-Service Aircraft for a Global Observing System (IAGOS) aircraft measurements are presented. A good agreement is found between MOPITT and MOZAIC/IAGOS measurements, consistent with results from earlier studies using different validation data and despite large variability in MOPITT CO total columns along the spatial footprint of the MOZAIC/IAGOS measurements. Validation results improve when taking the large spatial footprint of the MOZAIC/IAGOS data into account. No statistically significant drift was detected in the validation results over the period 2002–2010 at global, continental and local (airport) scales. Furthermore, for those situations where MOZAIC/IAGOS measurements differed from the MOPITT a priori, the MOPITT measurements clearly outperformed the MOPITT a priori data, indicating that MOPITT NIR retrievals add value to the MOPITT a priori. Results from a high spatial resolution simulation of the chemistry-transport model MOCAGE (MOdèle de Chimie Atmosphérique à Grande Echelle) showed that the most likely explanation for the large MOPITT variability along the MOZAIC-IAGOS profile flight path is related to spatio-temporal CO variability, which should be kept in mind when using MOZAIC/IAGOS profile measurements for validating satellite nadir observations.

Monitoring the lowermost tropospheric ozone with thermal infrared observations from a geostationary platform: performance analyses for a future dedicated instrument

Abstract. In this paper, we present performance analyses for a concept geostationary observing system called MAGEAQ (Monitoring the Atmosphere from Geostationary orbit for European Air Quality). The MAGEAQ mission is designed to include a TIR (thermal infrared) spectrometer and a broadband VIS (visible) radiometer; in this work we study only the TIR component (MAGEAQ-TIR). We have produced about 20 days of MAGEAQ-TIR tropospheric ozone pseudo-observations with a full forward and inverse radiative transfer pseudo-observations simulator. We have studied the expected sensitivity of MAGEAQ-TIR and we have found that it is able to provide a full single piece of information for the ozone column from surface to 6 km (about 1.0 DOF (degrees of freedom) and maximum sensitivity at about 3.0 km, on average), as well as a partially independent surface–3 km ozone column (about 0.6 DOF and maximum sensitivity at about 2.5 km, on average). Then, we have compared the tropospheric ozone profiles and the lower (surface–6 km) and lowermost (surface–3 km) tropospheric ozone column pseudo-observations to the target pseudo-reality, produced with the MOCAGE (MOdèle de Chimie Atmosphérique à Grande Echelle) chemistry and transport model. We have found very small to not significant average biases (< 1% in absolute value, for the surface–6 km TOC (tropospheric ozone column), and about −2 to −3 %, for the surface–3 km TOC) and small RMSEs (root mean square errors; about 1.3 DU (5%), for the surface–6 km TOC, and about 1.5 DU (10%), for the surface–3 km TOC). We have tested the performance of MAGEAQ-TIR at some selected small (0.2° × 0.2°) urban and rural locations. We have found that, while the vertical structures of the lower tropospheric ozone pseudo-reality are sometimes missed, MAGEAQ-TIR's lower and lowermost column pseudo-observations follow stunningly good the MOCAGE column pseudo-reality, with correlation coefficients reaching values of 0.9 or higher. Unprecedented retrieval performance for the lowermost tropospheric ozone column is shown. In any case, our MAGEAQ-TIR pseudo-observations are only partially able to replicate the MOCAGE pseudo-reality variability and temporal cycle at the very lowest layers (surface and 1 km altitude), especially at southern European urban locations, where the photochemistry signal is partially missed or shifted at higher altitudes. Temporal artifacts on the daily cycle are sometimes observed. Stratospheric-to-tropospheric exchanges during short time periods (of the order of 1 day) are detected by the MAGEAQ-TIR pseudo-observations.

Analysis of a rapid increase of stratospheric ozone during late austral summer 2008 over Kerguelen (49.4° S, 70.3° E)

Abstract. This paper reports on an increase of ozone event observed over Kerguelen (49.4° S, 70.3° E) in relationship with large-scale isentropic transport. This is evidenced by ground-based observations (co-localised radiosonde and SAOZ experiments) together with satellite global observations (Aura/MLS) assimilated into MOCAGE, a Méteo-France model. The study is based on the analyses of the first ozonesonde experiment never recorded at the Kerguelen site within the framework of a French campaign called ROCK that took place from April to August 2008. Comparisons and interpretations of the observed event are supported by co-localised SAOZ observations, by global mapping of tracers (O3, N2O and columns of O3) from Aura/MLS and Aura/OMI experiments, and by model simulations of Ertel Potential Vorticity initialised by the ECMWF (European Centre for Medium-Range Weather Forecasts) data reanalyses. Satellite and ground-based observational data revealed a consistent increase of ozone in the local stratosphere by mid-April 2008. Additionally, Ozone (O3) and nitrous oxide (N2O) profiles obtained during January–May 2008 using the Microwave Limb Sounder (MLS) aboard the Aura satellite are assimilated into MOCAGE (MOdèle de Chimie Atmosphérique à Grande Echelle), a global three-dimensional chemistry transport model of Météo-France. The assimilated total O3 values are consistent with SAOZ ground observations (within ±5%), and isentropic distributions of O3 match well with maps of advected potential vorticity (APV) derived from the MIMOSA model, a high-resolution advection transport model, and from the ECMWF reanalysis. The event studied seems to be related to the isentropic transport of air masses that took place simultaneously in the lower- and middle-stratosphere, respectively from the polar region and from the tropics to the mid-latitudes. In fact, the ozone increase observed by mid April 2008 resulted simultaneously: (1) from an equator-ward departure of polar air masses characterised with a high-ozone layer in the lower stratosphere (near the 475 K isentropic level), and (2) from a reverse isentropic transport from the tropics to mid- and high-latitudes in the upper stratosphere (nearby the 700 K level). The increase of ozone observed over Kerguelen from the 16-April ozonesonde profile is thus attributed to a concomitant isentropic transport of ozone in two stratospheric layers: the tropical air moving southward and reaching over Kerguelen in the upper stratosphere, and the polar air passing over the same area but in the lower stratosphere.

Cross-tropopause fluxes of ozone using assimilation of MOZAIC observations in a global CTM

Ozone measurements from Measurements of OZone and wAter vapour by aIrbus in-service airCraft (MOZAIC) have been assimilated into the global chemical transport model of Meteo France known as Modele de Chimie Atmospherique a Grande Echelle (MOCAGE). The assimilation makes improvements to the free model simulations of ozone in the upper troposphere and lower stratosphere, which are generally overestimated in the tropical region and underestimated in mid-latitudes. The tropical–subtropical gradient of ozone is also improved following assimilation and comparison with vertical profiles from ozonesondes suggests that the assimilation leads to a better representation of the vertical gradient around the tropopause. We use the assimilated fields to calculate a value for the flux of ozone across the tropopause. The net flux of ozone from stratosphere to troposphere is found to be 451 Tg yr -1 before assimilation and 383 Tg yr -1 after assimilation. The downward flux of ozone in the mid-latitudes exhibits an annual cycle with maximum flux occurring in early spring and minimum flux in autumn. DOI: 10.1111/j.1600-0889.2006.00243.x

Observed and modelled “chemical weather” during ESCOMPTE

The new MOdèle de Chimie Atmosphérique à Grande Echelle (MOCAGE) three-dimensional multiscale chemistry and transport model (CTM) has been applied to study heavy pollution episodes observed during the ESCOMPTE experiment. The model considers the troposphere and lower stratosphere, and allows the possibility of zooming from the planetary scale down to the regional scale over limited area subdomains. Like this, it generates its own time-dependent chemical boundary conditions in the vertical and in the horizontal. This paper focuses on the evaluation and quantification of uncertainties related to chemical and transport modelling during two intensive observing periods, IOP2 and IOP4 (June 20–26 and July 10–14, 2001, respectively). Simulations are compared to the database of four-dimensional observations, which includes ground-based sites and aircraft measurements, radiosoundings, and quasi-continuous measurements of ozone by LIDARs. Thereby, the observed and modelled day-to-day variabilities in air composition both at the surface and in the vertical have been assessed. Then, three sensitivity studies are conducted concerning boundary conditions, accuracy of the emission dataset, and representation of chemistry. Firstly, to go further in the analysis of chemical boundary conditions, results from the standard grid nesting set-up and altered configurations, relying on climatologies, are compared. Along with other recent studies, this work advocates the systematic coupling of limited-area models with global CTMs, even for regional air quality studies or forecasts. Next, we evaluate the benefits of using the detailed high-resolution emissions inventory of ESCOMPTE: improvements are noticeable both on ozone reactivity and on the concentrations of various species of the ozone photochemical cycle especially primary ones. Finally, we provide some insights on the comparison of two simulations differing only by the parameterisation of chemistry and using two state-of-the-art chemical schemes for regional photochemical modelling. Regional air quality modelling is found to be highly sensitive to the emission inventory dataset and also to the vertical and horizontal boundary conditions and detailed representation of chemistry. Interestingly enough, they infer the same range of errors compared to total model errors.