AIR POLLUTION IN THE CZECH REPUBLIC IN 2002

Czech Hydrometeorological Institute - Air Quality Protection Division




 LIST OF FIGURES

Fig. –1 Scheme of ISKOs links to data sources and co-operating systems
Fig. 1.1 Total emissions of principal pollutants in the Czech Republic between 1990 and 2002
Fig. 1.2 Fuel consumption in REZZO 3 sources, 1992–2002
Fig. 1.3 Changes in residential heating in 2002 as compared to 1991
Fig. 1.4 Particulate emission density from 5x5 km squares, 2001
Fig. 1.5 Sulphur dioxide emission density from 5x5 km squares, 2001
Fig. 1.6 Nitrogen oxide emission density from 5x5 km squares, 2001
Fig. 1.7 CxHy emission density from 5x5 km squares, 2001
Fig. 2.1.1 Major station networks of ambient air quality monitoring, 2002
Fig. 2.1.2 Monitoring of principal pollutants in selected organisations – development
Fig. 2.2.1 4th highest 24-hour concentrations and annual average concentrations of SO2 in 1992–2002 at selected stations
Fig. 2.2.2 Field of the 4th highest 24-hour concentration of SO2 in 2002
Fig. 2.2.3 Stations with the highest hourly concentrations of SO2 in 2002
Fig. 2.2.4 Stations with the highest 24-hour concentrations of SO2 in 2002
Fig. 2.2.5 36th highest 24-hour concentrations and annual average concentrations of PM10 in 1994–2002 at selected stations
Fig. 2.2.6 Field of the 36th highest 24-hour concentration of PM10 in 2002
Fig. 2.2.7 Field of annual average concentration of PM10 in 2002
Fig. 2.2.8 Stations exceeding LV+MT for 24-hour concentrations of PM10 in 2002
Fig. 2.2.9 19th highest hourly concentrations and annual average concentrations of NO2 in 1992–2002 at selected stations
Fig. 2.2.10 Field of annual average concentration of NO2 in 2002
Fig. 2.2.11 Stations with the highest hourly concentrations of NO2 in 2002
Fig. 2.2.12 Annual average concentrations of lead in the ambient air in 1992–2002 at selected stations
Fig. 2.2.13 1/7/14-day average concentrations of lead in the ambient air at selected stations in 2002
Fig. 2.2.14 Maximum 8-hour moving average concentrations of CO in 1994–2002 at selected stations
Fig. 2.2.15 Stations with the highest values of maximum 8-hour moving average concentrations of CO in 2002
Fig. 2.2.16 Annual average concentrations of benzene in 1999–2002 at selected stations
Fig. 2.2.17 24-hour concentrations at the stations with the highest annual benzene concentrations in 2002
Fig. 2.2.18 26th highest values of maximum 8-hour moving average of ozone concentrations in 1992–2002 at selected stations
Fig. 2.2.19 Field of the 76th highest maximum daily 8-hour moving ozone concentration in 2000–2002
Fig. 2.2.20 Stations with the highest values of maximum daily 8-hour moving average concentrations of ozone in 2002
Fig. 2.2.21 Annual average concentrations of cadmium in the ambient air in 1992–2002 at selected stations
Fig. 2.2.22 Field of annual average concentration of cadmium in the ambient air in 2002
Fig. 2.2.23 1/7/14-day average concentrations of cadmium in the ambient air at selected stations in 2002
Fig. 2.2.24 Annual average concentrations of arsenic in the ambient air in 1992–2002 at selected stations
Fig. 2.2.25 Field of annual average concentration of arsenic in the ambient air in 2002
Fig. 2.2.26 1/7/14-day average concentrations of arsenic in the ambient air at selected stations in 2002
Fig. 2.2.27 Annual average concentrations of nickel in the ambient air in 1992–2002 at selected stations
Fig. 2.2.28 1/7/14-day average concentrations of nickel in the ambient air at selected stations in 2002
Fig. 2.2.29 Annual average concentrations of benzo(a)pyrene in 1997–2002 at selected stations
Fig. 2.2.30 Field of annual average concentration of benzo(a)pyrene in the ambient air in 2002
Fig. 2.2.31 24-hour concentrations at the stations with the highest annual concentrations of benzo(a)pyrene in 2002
Fig. 2.2.32 Areas/administrative units with deteriorated air quality with regard to health protection limit values, ozone excluded, 2002
Fig. 2.2.33 Winter average concentrations of SO2 in 1992/1993–2002/2003 at selected stations
Fig. 2.2.34 Field of average concentration of SO2 in the winter period 2001/2002
Fig. 2.2.35 Annual average concentrations of NOx in 1992–2002 at selected stations
Fig. 2.2.36 Field of annual average concentration of NOx in 2002
Fig. 2.2.37 AOT40 values of ozone in 1995–2002 at selected stations
Fig. 2.2.38 Field of AOT40 value of ozone in 2002
Fig. 2.2.39 Areas with deteriorated air quality with regard to SO2 and NOx limit values for the protection of ecosystems/vegetation pursuant to the Act No. 86/2002 Coll., 2002
Fig. 2.2.40 Areas with deteriorated air quality for ecosystems/vegetation, exceedence of limit value for AOT40, 2002
Fig. 2.3.1 Annual arithmetic means of concentrations at stations, SPM, 2002
Fig. 2.3.2 Fields of annual arithmetic means of concentrations with presentation of measured values at stations, nitrogen oxides, 2002
Fig. 2.3.3 95th percentiles of daily concentrations at stations, nitrogen oxides, 2002
Fig. 2.3.4 Annual assessment for 1982–2002 in Prague, Northwest Region and Moravian-Silesian Region
Fig. 2.3.5 Assessment of 1982/1983–2002/2002 winter seasons in Prague, Northwest Region and Moravian-Silesian Region
Fig. 2.4.1 Course of maximum daily temperatures, their long-term average and daily total precipitation at Prague-Libuš station, occurrence of ozone concentrations exceeding 180 μg.m-3 on the territory of the Czech Republic 1.6.2002–15.9.2002
Fig. 2.4.2 Spatial distribution of maximum hourly concentrations of NO2 a O3, 10. 7. 2002
Fig. 2.4.3 Distribution of maximum hourly ozone concentrations on the territory of the Czech Republic, 10 July 2002, and three-hour average ozone concentrations in Austria, 10 July 2002 at 16:00 CEST.
Fig. 2.4.4 Spatial distribution of maximum hourly concentrations of NO2 a O3, 23. 8.2002
Fig. 3.1 Station networks monitoring precipitation quality and atmospheric deposition, 2002
Fig. 3.2 Fields of annual wet deposition of sulphur (SO2-4 - S), 2002
Fig. 3.3 Fields of annual dry deposition of sulphur (SO2 - S), 2002
Fig. 3.4 Fields of annual total deposition of sulphur, 2002
Fig. 3.5 Fields of annual throughfall deposition of sulphur, 2002
Fig. 3.6 Fields of annual wet deposition of nitrogen (NO-3 - N), 2002
Fig. 3.7 Fields of annual wet deposition of nitrogen (NH+4 - N), 2002
Fig. 3.8 Fields of annual total wet deposition of nitrogen, 2002
Fig. 3.9 Fields of annual dry deposition of nitrogen (NOx - N), 2002
Fig. 3.10 Fields of annual total deposition of nitrogen, 2002
Fig. 3.11 Fields of annual wet deposition of hydrogen ions, 2002
Fig. 3.12 Fields of annual dry deposition of hydrogen ions corresponding to SO2 and NOx deposition, 2002
Fig. 3.13 Fields of annual total deposition of hydrogen ions, 2002
Fig. 3.14 Fields of annual wet deposition of fluoride ions, 2002
Fig. 3.15 Fields of annual wet deposition of lead ions, 2002
Fig. 3.16 Fields of annual dry deposition of lead, 2002
Fig. 3.17 Fields of annual wet deposition of cadmium ions, 2002
Fig. 3.18 Fields of annual dry deposition of cadmium, 2002
Fig. 3.19 Fields of annual wet deposition of nickel ions, 2002
Fig. 3.20 Annual wet deposition at selected stations between 1990 and 2002, the Czech Republic
Fig. 3.21 Annual deposition of sulphur and oxidated forms of nitrogen in the Czech Republic, 1995-2002