Biogenic volatile organic compounds (BVOC) emitted from vegetation are important for the formation of secondary pollutants such as ozone and secondary organic aerosols (SOA) in the atmosphere. Therefore, BVOC emission are an important input for air quality models. To model these emissions with high spatial resolution, the accuracy of the underlying vegetation inventory is crucial. We present a BVOC emission model that accommodates different vegetation inventories and uses satellite-based measurements of greenness instead of pre-defined vegetation periods. This approach to seasonality implicitly treats effects caused by water or nutrient availability, altitude and latitude on a plant stand. Additionally, we test the influence of proposed seasonal variability in enzyme activity on BVOC emissions. In its present setup, the emission model calculates hourly emissions of isoprene, monoterpenes, sesquiterpenes and the oxygenated volatile organic compounds (OVOC) methanol, formaldehyde, formic acid, ethanol, acetaldehyde, acetone and acetic acid. In this study, emissions based on three different vegetation inventories are compared with each other and diurnal and seasonal variations in Europe are investigated for the year 2006. Two of these vegetation inventories require information on tree-cover as an input. We compare three different land-cover inventories (USGS GLCC, GLC2000 and Globcover 2.2) with respect to tree-cover. The often-used USGS GLCC land-cover inventory leads to a severe reduction of BVOC emissions due to a potential miss-attribution of broad-leaved trees and reduced tree-cover compared to the two other land-cover inventories. To account for uncertainties in the land-cover classification, we introduce land-cover correction factors for each relevant land-use category to adjust the tree-cover. The results are very sensitive to these factors within the plausible range. For June 2006, total monthly BVOC emissions decreased up to −27% with minimal and increased up to +71% with maximal factors, while in January 2006, the changes in monthly BVOC emissions were −54 and +56% with minimal and maximal factors, respectively. The new seasonality approach leads to a reduction in the annual emissions compared with non-adjusted data. The strongest reduction occurs in OVOC (up to −32%), the weakest in isoprene (as little as −19%). If also enzyme seasonality is taken into account, however, isoprene reacts with the steepest decrease of annual emissions, which are reduced by −44% to −49%, annual emissions of monoterpenes reduce between −30 and −35%. The sensitivity of the model to changes in temperature depends on the climatic zone but not on the vegetation inventory. The sensitivity is higher for temperature increases of 3 K (+31% to +64%) than decreases by the same amount (−20 to −35%). The climatic zones "Cold except summer" and "arid" are most sensitive to temperature changes in January for isoprene and monoterpenes, respectively, while in June, "polar" is most sensitive to temperature for both isoprene and monoterpenes. ...

Abstract. The results of a comparison exercise of radiative transfer models (RTM) of various international research groups for Multiple AXis Differential Optical Absorption Spectroscopy (MAX-DOAS) viewing geometry are presented. Besides the assessment of the agreement between the different models, a second focus of the comparison was the systematic investigation of the sensitivity of the MAX-DOAS technique under various viewing geometries and aerosol conditions. In contrast to previous comparison exercises, box-air-mass-factors (box-AMFs) for different atmospheric height layers were modelled, which describe the sensitivity of the measurements as a function of altitude. In addition, radiances were calculated allowing the identification of potential errors, which might be overlooked if only AMFs are compared. Accurate modelling of radiances is also a prerequisite for the correct interpretation of satellite observations, for which the received radiance can strongly vary across the large ground pixels, and might be also important for the retrieval of aerosol properties as a future applicationCorrespondence to: T. Wagner (thomas.wagner@iup.uni-heidelberg.de) of MAX-DOAS. The comparison exercises included different wavelengths and atmospheric scenarios (with and without aerosols). The strong and systematic influence of aerosol scattering indicates that from MAX-DOAS observations also information on atmospheric aerosols can be retrieved. During the various iterations of the exercises, the results from all models showed a substantial convergence, and the final data sets agreed for most cases within about 5%. Larger deviations were found for cases with low atmospheric optical depth, for which the photon path lengths along the line of sight of the instrument can become very large. The differences occurred between models including full spherical geometry and those using only plane parallel approximation indicating that the correct treatment of the Earth's sphericity becomes indispensable. The modelled box-AMFs constitute an universal data base for the calculation of arbitrary (total) AMFs by simple convolution with a given trace gas concentration profile. Together with the modelled radiances and the specified settings for the various exercises, they can serve as test cases for future RTM developments.Published by Copernicus GmbH on behalf of the European Geosciences Union.

Abstract. Measurements of airborne particles with aerodynamic diameter of 10 µm or less (PM 10 ) and meteorological observations are available from 13 stations distributed throughout Switzerland and representing different site types. The effect of all available meteorological variables on PM 10 concentrations was estimated using Generalized Additive Models. Data from each season were treated separately. The most important variables affecting PM 10 concentrations in winter, autumn and spring were wind gust, the precipitation rate of the previous day, the precipitation rate of the current day and the boundary layer depth. In summer, the most important variables were wind gust, Julian day and afternoon temperature. In addition, temperature was important in winter. A "weekend effect" was identified due to the selection of variable "day of the week" for some stations. Thursday contributes to an increase of 13% whereas Sunday contributes to a reduction of 12% of PM 10 concentrations compared to Monday on average over 9 stations for the yearly data. The estimated effects of meteorological variables were removed from the measured PM 10 values to obtain the PM 10 variability and trends due to other factors and processes, mainly PM 10 emissions and formation of secondary PM 10 due to trace gas emissions. After applying this process, the PM 10 variability was much lower, especially in winter where the ratio of adjusted over measured mean squared error was 0.27 on average over all considered sites. Moreover, PM 10 trends in winter were more negative after the adjustment for meteorology and they ranged between −1.25 µg m

Abstract. The trends and variability of PM10, PM2.5 and PMcoarse concentrations at seven urban and rural background stations in five European countries for the period between 1998 and 2010 were investigated. Collocated or nearby PM measurements and meteorological observations were used in order to construct Generalized Additive Models, which model the effect of each meteorological variable on PM concentrations. In agreement with previous findings, the most important meteorological variables affecting PM concentrations were wind speed, wind direction, boundary layer depth, precipitation, temperature and number of consecutive days with synoptic weather patterns that favor high PM concentrations. Temperature has a negative relationship to PM2.5 concentrations for low temperatures and a positive relationship for high temperatures. The stationary point of this relationship varies between 5 and 15 °C depending on the station. PMcoarse concentrations increase for increasing temperatures almost throughout the temperature range. Wind speed has a monotonic relationship to PM2.5 except for one station, which exhibits a stationary point. Considering PMcoarse, concentrations tend to increase or stabilize for large wind speeds at most stations. It was also observed that at all stations except one, higher PM2.5 concentrations occurred for east wind direction, compared to west wind direction. Meteorologically adjusted PM time series were produced by removing most of the PM variability due to meteorology. It was found that PM10 and PM2.5 concentrations decrease at most stations. The average trends of the raw and meteorologically adjusted data are −0.4 μg m−3 yr−1 for PM10 and PM2.5 size fractions. PMcoarse have much smaller trends and after averaging over all stations, no significant trend was detected at the 95% level of confidence. It is suggested that decreasing PMcoarse in addition to PM2.5 can result in a faster decrease of PM10 in the future. The trends of the 90th quantile of PM10 and PM2.5 concentrations were examined by quantile regression in order to detect long term changes in the occurrence of very large PM concentrations. The meteorologically adjusted trends of the 90th quantile were significantly larger (as an absolute value) on average over all stations (−0.6 μg m−3 yr−1).

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