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A method to generate near real time UV-Index maps of Austria

A method is presented that combines individual ground based ultraviolet (UV) measurements and satellite data from MSG (Meteosat Second Generation) to generate a UV-Index map all over the region of Austria. Cloud modification factors (CMFs) gathered from satellite images give an area wide information of the cloud situation but compared to ground based measurements significant discrepancies have been found. These discrepancies are especially large for high mountain stations but also for low altitude sites differences between satellite derived and ground based data in the order of 15% have been found. To overcome these discrepancies a correction procedure based on the correlation of both data sets at the pixel of the measurement stations is developed. The uncertainty of the final UV-Index map is evaluated exemplarily for the pixel of the measurement sites Bad Vöslau and München by eliminating the information of both sites from the UV-Index map generation process and comparing afterwards calculated and measured results. More than 5000 maps for all weather conditions have been evaluated leading to a mean agreement of 1.02 (standard deviation ±0.31, Bad Vöslau) and 1.01 (standard deviation ±0.34, München) between calculated and measured UV-Indexes.
Seasonal variation of nocturnal temperatures between 1 and 105 km altitude at 54° N observed by lidar

Temperature soundings are performed by lidar at the mid-latitude station of Kühlungsborn (Germany, 54° N, 12° E). The profiles cover the complete range from the lower troposphere (~1 km) to the lower thermosphere (~105 km) by simultaneous and co-located operation of a Rayleigh-Mie-Raman lidar and a potassium resonance lidar. Observations have been done during 266 nights between June 2002 and July 2007, each of 3–15 h length. This large and unique data set provides comprehensive information on the altitudinal and seasonal variation of temperatures from the troposphere to the lower thermosphere. The remaining day-to-day-variability is strongly reduced by harmonic fits at constant altitude levels and a representative data set is achieved. This data set reveals a two-level mesopause structure with an altitude of about 86–87 km (~144 K) in summer and ~102 km (~170 K) during the rest of the year. The average stratopause altitude is ~48 km throughout the whole year, with temperatures varying between 258 and 276 K. From the fit parameters amplitudes and phases of annual, semi-annual, and quarter-annual variations are derived. The amplitude of the annual component is largest with amplitudes of up to 30 K in 85 km, while the quarter-annual variation is smallest and less than 3 K at all altitudes. The lidar data set is compared with ECMWF temperatures below about 70 km altitude and reference data from the NRLMSISE-00 model above. Apart from the temperature soundings the aerosol backscatter ratio is measured between 20 and 35 km. The seasonal variation of these values is presented here for the first time.
Polar organic tracers in PM2.5 aerosols from forests in eastern China

Photooxidation products of biogenic volatile organic compounds, mainly isoprene and monoterpenes, are significant sources of atmospheric particulate matter in forested regions. The objectives of this study were to examine time series and diel variations of polar organic tracers for the photooxidation of isoprene and α-pinene to investigate whether they are linked with meteorological parameters or trace gases, and to determine their carbon contributions. In addition, the biogenic secondary organic carbon contributions from isoprene were estimated. PM2.5 (particulate matter with an aerodynamic diameter <2.5 μm) aerosol samples were collected from forests in eastern China and compared with data from forested sites in Europe and America. Aerosol sampling was conducted at four sites located along a gradient of ecological succession in four different regions, i.e. Changbai Mountain Nature Reserve (boreal-temperate), Chongming National Forest Park (temperate), Dinghu Mountain Nature Reserve (subtropical) and Jianfengling Nature Reserve in Hainan (tropical) during summer periods when the meteorological conditions are believed to be favorable for photochemical processes. Fifty PM2.5 samples were collected; eighteen organic compounds, organic carbon (OC), elemental carbon and trace gases were measured. Results indicate that the concentration trends of the secondary organic compounds reflected those of the trace gases and meteorological parameters. Very good correlations between the sum concentrations of isoprene oxidation products and atmospheric SO2, O3, NO2, NOx, as well as CO2, at the Changbai site were found. The secondary OC due to isoprene was relatively high in tropical Hainan (0.27 μgC/m3) where isoprene-emitting broadleaf species are dominant, but was comparable in boreal Changbai (0.32 μgC/m3) where coniferous species are prevalent. The contribution of malic acid, which may have both biogenic and anthropogenic sources, to the OC mass was comparable at the four sites.
Significant impact of the East Asia monsoon on ozone seasonal behavior in the boundary layer of Eastern China and the west Pacific region

The impact of the East Asia monsoon on the seasonal behavior of O3 in the boundary layer of Eastern China and the west Pacific region was analyzed for 2004–2006 by means of full-year nested chemical transport model simulations and continuous observational data obtained from three inland mountain sites in central and eastern China and three oceanic sites in the west Pacific region. The basic common features of O3 seasonal behaviors over all the monitoring sites are the pre- and post-monsoon peaks with a summer trough. Such bimodal seasonal patterns of O3 are predominant over the region with strong summer monsoon penetration, and become weaker or even disappear outside the monsoon region. The seasonal/geographical distribution of the pre-defined monsoon index indicated that the East Asia summer monsoon is responsible for the bimodal seasonal O3 pattern, and also partly account for the differences in the O3 seasonal variations between the inland mountain and oceanic sites. Over the inland mountain sites, the O3 concentration increased gradually from the beginning of the year, reached a maximum in June, decreased rapidly to the summer valley in July or August, and then peaked in September or October, thereafter decreased gradually again. Over the oceanic sites, O3 abundance showed a similar increasing trend beginning in January, but then decreased gradually from the end of March, followed by a wide trough with the minimum in July and August and a small peak in October or November. A sensitivity analysis performed by setting China-emission to zero revealed that the chemically produced O3 from China-emission contributed substantially to the O3 abundance, particularly the pre- and post-monsoon O3 peaks, over China mainland. We found that China-emission contributed more than 40% to total boundary layer O3 during summertime (60–70% in July) and accounted for about 40 ppb of each peak value over the inland region if without considering the effect of the nonlinear chemical productions. In contrast, over the oceanic region in the high monsoon index zone, the contribution of China-emission to total boundary layer O3 was always less than 20% (<10 ppb), and less than 10% in summer.
Characterizing ozone production and response under different meteorological conditions in Mexico City

Photochemistry in polluted atmospheres, particularly the formation of ozone (O3), depends not only on pollutant emissions, but also on meteorological conditions. In this study a 3-D chemical transport model CAMx was employed to investigate the O3 formation and its response to emissions reduction under three distinctively different meteorological conditions in the Mexico City Metropolitan Area during the MCMA-2003 field measurement campaign. The O3 formation characteristics and sensitivity to emissions change were found to be weakly dependent on the meteorological conditions. The evolution of O3 formation and its sensitivity to NOx and VOC levels were also examined along the photochemical plume transport pathway. The midday O3 production was found to undergo a rapid increase in a narrow range of chemical aging, while downwind plumes were characterized with low and constant O3 production, and plumes along their transport pathway were characterized by a combination of the two. The O3 formation was more VOC sensitive near the source area, but as the plume became chemically aged, O3 formation became progressively VOC insensitive and more NOx sensitive.
Carbonyl sulfide in air extracted from a South Pole ice core: a 2000 year record

In this study, we present carbonyl sulfide (COS) measurements from an ice core drilled near South Pole, East Antarctica (SPRESSO). The samples are from 135–291 m, with estimated mean COS ages ranging from 278 to 2155 years before present (defined as 2000 C.E.). When combined with the previous records of COS from Antarctic ice cores and firn air, the current data provide a continuous record of COS extending beyond the last two millennia. The general agreement between ice cores, firn air, and modern air measurements supports the idea that polar ice is a valid archive for paleoatmospheric COS. The average COS mixing ratio of the SPRESSO data set is (331±18) ppt (parts per trillion in mol/mol, ±1σ, n=100), excluding 6 outliers. These data confirm earlier firn air and ice core measurements indicating that the late 20th century COS levels of 500 ppt are greatly increased over preindustrial levels and represent the highest atmospheric levels over the past 2000 years. The data also provide evidence of climate-related variability on centennial time-scales, with relative maxima at the peaks of Medieval Climate Anomaly and Little Ice Age. There is evidence for a long-term increasing trend in COS of 1.8 ppt per 100 years. Further ice core studies will be needed to determine whether this trend reflects secular variability in atmospheric COS, or a slow post-depositional chemical loss of COS in the ice core.
Large-scale planetary disturbances in stratospheric temperature at high-latitudes in the southern summer hemisphere

The global structure and propagation of large-scale (periods >5 days) waves in the Southern Hemisphere summer (December 2006–February 2007) at 60° S–75° S latitude are examined using temperature data from GPS radio occultation measurements by COSMIC/FORMOSAT 3 satellite constellation at 20 km and 30 km altitude. Spectral analysis has revealed eastward propagating planetary scale perturbations with wavenumbers 1 and 2 and periods of 10, 16 and 23 days, and stationary waves with wavenumbers 1 and 2. The results obtained show a very dynamically active Antarctic summer stratosphere. The novel aspect of the work is in the use of the GPS COSMIC data providing multiple local times each day, thus allowing large-scale wave analysis at high Southern latitudes and revealing planetary wave activity not normally observed in summer, but more consistent with late winter and spring conditions in the stratosphere.
Evaluation of the MERIS aerosol product over land with AERONET

The Medium Resolution Imaging Spectrometer (MERIS) launched in February 2002 on-board the ENVISAT spacecraft is making global observations of top-of-atmosphere (TOA) radiances. Aerosol optical properties are retrieved over land using Look-Up Table (LUT) based algorithm and surface reflectances in the blue and the red spectral regions. We compared instantaneous aerosol optical thicknesses retrieved by MERIS in the blue and the red at locations containing sites within the Aerosol Robotic Network (AERONET). Between 2002 and 2005, a set of 500 MERIS images were used in this study. The result shows that, over land, MERIS aerosol optical thicknesses are well retrieved in the blue and poorly retrieved in the red, leading to an underestimation of the Angstrom coefficient. Correlations are improved by applying a simple criterion to avoid scenes probably contaminated by thin clouds. To investigate the weakness of the MERIS algorithm, ground-based radiometer measurements have been used in order to retrieve new aerosol models, based on their Inherent Optical Properties (IOP). These new aerosol models slightly improve the correlation, but the main problem of the MERIS aerosol product over land can be attributed to the surface reflectance model in the red.
Traffic restrictions in Beijing during the Sino-African Summit 2006: aerosol size distribution and visibility compared to long-term in situ observations

Based on the long-term in-situ observations of aerosol particle number size distributions and meteorological parameters, the measures of traffic restriction during the Sino-African Summit (4–6 November 2006) in Beijing, China have been found to be efficient in reducing the number concentration of aerosol particles, in particular Aitken and accumulation mode particles, and in improving the visibility when local emissions dominated. The influence of traffic restrictions on the particle concentrations differed for different particle sizes. More significant effects on fine particles with diameters ranging from 40 to 500 nm have been found. Based on statistical analysis of long-term observations, under comparable weather conditions, the number concentrations of the particles in Aitken and accumulation modes seemingly were reduced by 20–60% when the traffic restrictions were in place. This change may be mainly due to the reduction of secondary particle contributions. However, it is worth to notice that the reduction of 60% might overestimate the effect of the measures of traffic control, due to the inherent data shortage with very high wind speeds in the comparison data population. Our size-dependent aerosol data also indicate that measures led to reductions in particulate air pollution in the optically most important diameter range, whereas further vehicle restriction measures might lead to an increase in ultrafine particle formation if the condensational sink further decreased. Assuming that there were no traffic restrictions and with normal levels of the vehicle emissions, the visibilities during the Summit would have been lower by about 20–45%. The fact that over 95% cases with visibility range lower than 5 km during 2004 to 2007 occurred when the local wind speed was lower than 3 m s−1 may suggest that the importance of the emission restrictions is highest when the wind speed is lower than 3 m s−1, concerning the improvement of serious low visibility situations in Beijing.
High spatial resolution measurements of NO2 applying Topographic Target Light scattering-Differential Optical Absorption Spectroscopy (ToTaL-DOAS)

Topographic Target Light scattering – Differential Optical Absorption Spectroscopy (ToTaL-DOAS), also called Target-DOAS, is a novel experimental procedure to retrieve trace gas concentrations present in the low atmosphere. Scattered sunlight (diffuse or specular) reflected from natural or artificial targets located at different distances are analyzed to retrieve the spatial distribution of the concentration of different trace gases like NO2, SO2 and others. We report high spatial resolution measurements of NO2 mixing ratios in the city of Montevideo (Uruguay) observing three buildings as targets with a Mini-DOAS instrument. Our instrument was 146 m, 196 m, and 280 m apart from three different buildings located along a main Avenue. We obtain temporal variation of NO2 mixing ratios between 30 ppb and 65 ppb from measurements of November 2007 and mixing ratios up to 50 ppb from measurements of August and September 2008. Our measurements demonstrate that ToTaL-DOAS observations can be made over relative short distances. In polluted air masses, the retrieved absorption signal was found to be sufficiently strong to allow measurements over distances in the range of several tens of meters.