LIST OF FIGURES

Fig. 1 Areas with exceeding of the health protection limit values for selected groups of pollutants, 2014
Fig. I.1 Major station networks of ambient air quality monitoring, 2014
Fig. I.2 The zones and agglomerations for ambient air quality assessment and evaluation of ambient air pollution level according to the Act No. 201/2012 Coll. On Clear Air Protection, as amended
Fig. II.1 The development of total emissions, 1990–2001
Fig. II.2 The development of total emissions, 2002–2013
Fig. II.3 The output of basic industrial products, 1990–2013
Fig. II.4 Fuel consumption in REZZO 3 sources, 1990–2014
Fig. III.1 Annual heating seasons in the CR expressed in degree days (D21) and their average for the period 1984–2013
Fig. III.2 Annual course of degree days in the territory of the CR in the heating season 2014 (I–V, IX–XII) in comparison with the average for 1984–2013
Fig. III.3 Temperature, dispersion conditions, and concentrations of PM10 and O3 in the agglomeration of Ostrava/Karviná/Frýdek-Místek, 2014
Fig. III.4 Annual course of the occurrence of dispersion conditions in the CR and agglomerations, 2014
Fig. IV.1.1 Field of the 36th highest 24-hour concentration of PM10, 2014
Fig. IV.1.2 Field of annual average concentration of PM10, 2014
Fig. IV.1.3 Numbers of exceedances of the limit value for 24-hour concentration of PM10, 2014
Fig. IV.1.4 Field of annual average concentration of PM2.5, 2014
Fig. IV.1.5 36th highest 24-hour concentrations and annual average concentrations of PM10 at selected stations with UB, SUB, T and I classification, 2004–2014
Fig. IV.1.6 36th highest 24-hour concentrations and annual average concentrations of PM10 at selected rural (R) stations, 2004–2014
Fig. IV.1.7 Annual average concentrations of PM2.5 in the ambient air at selected stations, 2004–2014
Fig. IV.1.8 Share of localities with the exceedance of the limit value for 24-hour concentration of PM10 and annual average concentrations of PM10 and PM2.5, 2000–2014
Fig. IV.1.9 Five-year average of annual average concentrations of PM10, 2010–2014
Fig. IV.1.10 Five-year average of annual average concentrations of PM2.5, 2010–2014
Fig. IV.1.11 Annual course of average monthly concentrations of PM10 (averages for the given type of station), 2014
Fig. IV.1.12 Annual course of average monthly concentrations of PM2.5 (averages for the given type of station), 2014
Fig. IV.1.13 Average monthly PM2.5/PM10 ratio, 2014
Fig. IV.1.14 Stations with the highest exceedance of LV for 24-hour concentrations of PM10, 2014
Fig. IV.1.15 Trends of PM10 annual characteristics in the Czech Republic, 2000–2014
Fig. IV.1.16 Trends of PM2.5 annual characteristics in the Czech Republic, 2005–2014
Fig. IV.1.17 Trends of selected characteristics of PM10 (index, year 2000 = 100), 2000–2014 and PM2.5 (index, year 2005 = 100), 2005–2014
Fig. IV.1.18 Total emissions of PM10 sorted out by NFR sectors, 2013
Fig. IV.1.19 The development of PM10 total emissions, 2007–2013
Fig. IV.1.20 Total emissions of PM2.5 sorted out by NFR sectors, 2013
Fig. IV.1.21 The development of PM2.5 total emissions, 2007–2013
Fig. IV.1.22 PM10 emission density from 5x5 km squares, 2013
Fig. IV.1.23 PM2.5 emission density from 5x5 km squares, 2013
Fig. IV.1.24 Numerical size distribution of aerosol particles (median, 25th and 75th percentile, 5th and 95th percentile) measured at the Košetice observatory over a period of five years (Zíková et al. 2014)
Fig. IV.1.25 Numerical size distribution of aerosol particles (median, 25th and 75th percentile, 5th and 95th percentile) measured at the station Ústí nad Labem-město for 7 size categories over the period of 2012–2014
Fig. IV.1.26 Average monthly concentrations of EC and OC at the Košetice observatory, 2009–2014
Fig. IV.1.27 Monthly variation of average concentrations of EC and OC at the Košetice observatory, 2009–2014
Fig. IV.1.28 Annual progression of concentrations of BC in PM1 measured at the Ústí nad Labem-centrum station, 2013–2014
Fig. IV.2.1 Field of annual average concentration of benzo[a]pyrene, 2014
Fig. IV.2.2 Annual average concentrations of benzo[a]pyrene in the ambient air at selected stations, 2004–2014
Fig. IV.2.3 Five-year average of annual average concentrations of benzo[a]pyrene, 2010–2014
Fig. IV.2.4 Trends of benzo[a]pyrene annual characteristics in the Czech Republic, 2006–2014
Fig. IV.2.5 Annual course of average monthly concentrations of benzo[a]pyrene (averages for the given type of station), 2014
Fig. IV.2.6 Average monthly concentrations of benzo[a]pyrene and PM10 particles at individual localities in winter months, 2014
Fig. IV.2.7 Concentrations of benzo[a]pyrene and PM10 particles at individual localities in winter months, 2010–2014
Fig. IV.2.8 24-hour concentrations at the stations with the highest annual concentrations of benzo[a]pyrene, 2014
Fig. IV.2.9 Total emissions of benzo[a]pyrene sorted out by NFR sectors, 2013
Fig. IV.2.10 The development of benzo[a]pyrene total emissions, 2007–2013
Fig. IV.2.11 Benzo[a]pyrene emission density from 5x5 km squares, 2013
Fig. IV.3.1 Field of annual average concentration of NO2, 2014
Fig. IV.3.2 Five-year average of annual average concentrations of NO2, 2010–2014
Fig. IV.3.3 Field of annual average concentration of NOx , 2014
Fig. IV.3.4 Annual course of average monthly concentrations of NO2 (averages for the given type of station), 2014
Fig. IV.3.5 Trends of NO2 and NOx annual characteristics in the Czech Republic, 2000–2014
Fig. IV.3.6 Trends of selected characteristics of NO2 and NOx (index, year 2000 = 100), 2000–2014
Fig. IV.3.7 Stations with the highest hourly concentrations of NO2, 2014
Fig. IV.3.8 24-hour concentrations at the stations with the highest annual concentrations of NOx , 2014
Fig. IV.3.9 19th highest hourly concentrations and annual average concentrations of NO2 at selected stations, 2004–2014
Fig. IV.3.10 Annual average concentrations of NOx at selected rural stations, 2004–2014
Fig. IV.3.11 Total emissions of NOx sorted out by NFR sectors, 2013
Fig. IV.3.12 The development of NOx total emissions, 2007–2013
Fig. IV.3.13 Nitrogen oxide emission density from 5x5 km squares, 2013
Fig. IV.4.1 Field of the 26th highest maximum daily 8-hour running average of ground-level ozone concentration in three-year average, 2012–2014
Fig. IV.4.2 26th highest values of maximum daily 8-hour running average of ground-level ozone concentrations (three-year average) at selected stations, 2004–2014
Fig. IV.4.3 Annual course of average monthly concentrations of max. 8-hour running average of O3 (averages for the given type of station), 2014
Fig. IV.4.4 Field of AOT40 exposure index values, average of 5 years, 2010–2014
Fig. IV.4.5 Numbers of exceedances of the limit value for the maximum daily 8-hour running average of ground-level ozone concentrations in three-year average, 2012–2014
Fig. IV.4.6 Trends of O3 annual characteristics in the Czech Republic, 2000–2014
Fig. IV.4.7 Trends of selected characteristics of O3 (index, year 2000 = 100), 2000–2014
Fig. IV.4.8 Exposure index AOT40 values at selected stations, average of 5 years 2004–2014
Fig. IV.4.9 Annual exposure index AOT40 values at selected stations, 2010–2014
Fig. IV.5.1 Field of annual average concentration of benzene, 2014
Fig. IV.5.2 Annual average concentrations of benzene at selected stations, 2004–2014
Fig. IV.5.3 Five-year average of annual average concentrations of benzene, 2010–2014
Fig. IV.5.4 Trends of benzene annual characteristics in the Czech Republic, 2005–2014
Fig. IV.5.5 24-hour concentrations at the stations with the highest annual benzene concentrations, 2014
Fig. IV.6.1 Field of annual average concentration of cadmium in the ambient air, 2014
Fig. IV.6.2 Field of annual average concentration of arsenic in the ambient air, 2014
Fig. IV.6.3 Five-year average of annual average concentrations of cadmium, 2010–2014
Fig. IV.6.4 Five-year average of annual average concentrations of arsenic, 2010–2014
Fig. IV.6.5 Annual average concentrations of lead in the ambient air at selected stations, 2004–2014
Fig. IV.6.6 Annual average concentrations of cadmium in the ambient air at selected stations, 2004–2014
Fig. IV.6.7 Annual average concentrations of arsenic in the ambient air at selected stations, 2004–2014
Fig. IV.6.8 Annual average concentrations of nickel in the ambient air at selected stations, 2004–2014
Fig. IV.6.9 Trends of heavy metals annual characteristics in the Czech Republic, 2006–2014
Fig. IV.6.10 Total emissions of arsenic sorted out by NFR sectors, 2013
Fig. IV.6.11 The development of arsenic total emissions, 2007–2013
Fig. IV.6.12 Total emissions of nickel sorted out by NFR sectors, 2013
Fig. IV.6.13 The development of nickel total emissions, 2007–2013
Fig. IV.6.14 Total emissions of cadmium sorted out by NFR sectors, 2013
Fig. IV.6.15 The development of cadmium total emissions, 2007–2013
Fig. IV.6.16 Total emissions of lead sorted out by NFR sectors, 2013
Fig. IV.6.17 The development of lead total emissions, 2007–2013
Fig. IV.6.18 Arsenic emission density from 5x5 km squares, 2013
Fig. IV.6.19 Nickel emission density from 5x5 km squares, 2013
Fig. IV.6.20 Cadmium emission density from 5x5 km squares, 2013
Fig. IV.6.21 Lead emission density from 5x5 km squares, 2013
Fig. IV.7.1 Field of the 4th highest 24-hour concentration of SO2, 2014
Fig. IV.7.2 4th highest 24-hour concentrations and 25th highest hourly concentrations of SO2 at selected stations, 2004–2014
Fig. IV.7.3 Trends of SO2 annual characteristics in the Czech Republic, 2000–2014
Fig. IV.7.4 Trends of selected characteristics of SO2 (index, year 2000 = 100), 2000–2014
Fig. IV.7.5 Field of annual average concentration of SO2, 2014
Fig. IV.7.6 Field of average concentration of SO2 in the winter period 2014/2015
Fig. IV.7.7 Annual average concentrations of SO2 at selected rural stations, 2004–2014
Fig. IV.7.8 Winter average concentrations of SO2 at selected rural stations, 2004/2005–2014/2015
Fig. IV.7.9 Total emissions of SO2 sorted out by NFR sectors, 2013
Fig. IV.7.10 The development of SO2 total emissions, 2007–2013
Fig. IV.7.11 Sulphur dioxide emission density from 5x5 km squares, 2013
Fig. IV.8.1 Maximum daily 8-hour running average concentrations of CO at selected stations, 2004–2014
Fig. IV.8.2 Total emissions of CO sorted out by NFR sectors, 2013
Fig. IV.8.3 The development of CO total emissions, 2007–2013
Fig. IV.8.4 Carbon moNOx ide emission density from 5x5 km squares, 2013
Fig. IV.9.1.1 Annual course of average monthly concentrations of VOC, 2014
Fig. IV.9.1.2 Total emissions of VOC sorted out by NFR sectors, 2013
Fig. IV.9.1.3 The development of VOC total emissions, 2007–2013
Fig. IV.9.2.1 Total emissions of NH3 sorted out by NFR sectors, 2013
Fig. IV.9.2.2 The development of NH3 total emissions, 2007–2013
Fig. IV.9.3.1 Total emissions of mercury sorted out by NFR sectors, 2013
Fig. IV.9.3.2 The development of mercury total emissions, 2007–2013
Fig. V.1 Trends of SO2, NO2, CO (2000–2014) and benzene (2005–2014) annual characteristics at urban and suburban stations in agglomerations
Fig. V.2 Trends of PM10 (2000–2014), PM2.5 (2005–2014) and benzo[a]pyrene (2006–2014) annual characteristics at urban and suburban stations in agglomerations
Fig. V.1.1 Number of exceedances of 24-hour PM10 limit value and the 36th highest 24-hour concentration PM10 at individual types of stations, agglomeration of Prague, 2006–2014
Fig. V.1.2 Number of days with concentrations of PM10 > 50 µg.m-3 in individual months, incl. total number of exceedances, agglomeration of Prague, 2014
Fig. V.1.3 Average annual PM2.5 concentrations, agglomeration of Prague, 2004–2014
Fig. V.1.4 Numbers of exceedances of the hourly limit value for NO2 at the traffic station Prague 2-Legerova (hot spot), agglomeration of Prague, 2003–2014
Fig. V.1.5 Average annual benzo[a]pyrene concentrations, agglomeration of Prague, 2000–2014
Fig. V.1.6 Numbers of exceedances of the limit value of O3 in the average for three years, agglomeration of Prague, 2006–2014
Fig. V.1.7 Field of the annual concentration of NO2, agglomeration of Prague, 2014
Fig. V.1.8 Field of the 36th highest 24-hour concentration of PM10, agglomeration of Prague, 2014
Fig. V.1.9 Emissions of selected pollutants listed according to REZZO, agglomeration of Prague
Fig. V.2.1 Average annual PM10 concentrations in selected localities and at individual types of stations, agglomeration of Brno, 2006–2014
Fig. V.2.2 Average monthly PM10 concentrations, Kuchařovice, 2005–2014
Fig. V.2.3 Average annual PM2.5 concentrations, agglomeration of Brno, 2006–2014
Fig. V.2.4 Number of exceedances of 24-hour PM10 limit value in selected localities and 36th highest 24-hour concentration of PM10 at individual types of stations, agglomeration of Brno, 2006–2014
Fig. V.2.5 Number of days with concentrations of PM10 > 50 µg.m-3 in individual months, incl. total number of exceedances, agglomeration of Brno, 2014
Fig. V.2.6 Average monthly NO2 and PM10 concentrations, locality Brno-Úvoz (hot spot)
Fig. V.2.7 Average annual NO2 concentrations in selected localities and at individual types of stations, agglomeration of Brno, 2006–2014
Fig. V.2.8 Average annual benzo[a]pyrene concentrations, agglomeration of Brno, 2006–2014
Fig. V.2.9 Field of the annual concentration of NO2, agglomeration of Brno, 2014
Fig. V.2.10 Field of the 36th highest 24-hour concentration of PM10, agglomeration of Brno, 2014
Fig. V.3.1 Average annual PM10 concentrations in selected localities and at individual types of stations, agglomeration of Ostrava/Karviná/Frýdek-Místek, 2006–2014
Fig. V.3.2 Average annual PM2.5 concentrations, agglomeration of Ostrava/Karviná/Frýdek-Místek, 2004–2014
Fig. V.3.3 Number of days with concentrations of PM10 > 50 µg.m-3 in individual months, incl. total number of exceedances, agglomeration of Ostrava/Karviná/Frýdek-Místek, 2014
Fig. V.3.4 Number of exceedances of 24-hour limit value for PM10 in selected localities and the 36th highest 24-hour concentrations of PM10 at individual types of stations, agglomeration of Ostrava/Karviná/Frýdek-Místek, 2006–2014
Fig. V.3.5 Average annual NO2 concentrations in selected localities and at individual types of stations, agglomeration of Ostrava/Karviná/Frýdek-Místek, 2006–2014
Fig. V.3.6 Average annual benzo[a]pyrene concentrations, agglomeration of Ostrava/Karviná/Frýdek-Místek, 2000–2014
Fig. V.3.7 Number of exceedances of the limit value of O3 in the average for three years, agglomeration of Ostrava/Karviná/Frýdek-Místek, 2006–2014
Fig. V.3.8 Field of the annual concentration of NO2, agglomeration of Ostrava/Karviná/Frýdek-Místek, 2014
Fig. V.3.9 Field of the 36th highest 24-hour concentration of PM10, agglomeration of Ostrava/Karviná/Frýdek-Místek, 2014
Fig. V.4.1 Relative representation of values of the air quality index calculated based on hourly concentrations of NO2, PM10 and O3 at urban and suburban automated stations, 2014
Fig. VI.1 SWRS areas and representative stations for PM10
Fig. VI.2 SWRS areas and representative stations for O3
Fig. VI.3 SWRS areas and representative stations for SO2
Fig. VI.4 SWRS areas and representative stations for NO2
Fig. VI.5 Smog situations and regulations for PM10 in the SWRS areas in which at least one smog situation was announced, 2014
Fig. VI.6 The episode with high ozone concentrations at the station Prague-Libuš, June 2014
Fig. VI.7 The episodes with high PM10 concentrations in the agglomeration of Ostrava/Karviná/Frýdek-Místek without Třinec area, December 2014
Fig. VII.1 Areas with exceeding of the health protection limit values, ground-level ozone excluded, 2014
Fig. VII.2 Areas with exceeding of the health protection limit values, incl. ground-level ozone, 2014
Fig. VII.3 Limit value exceedances in the Czech Republic, % of the area, 2006–2014
Fig. VII.4 Areas with exceeding of the ecosystems/vegetation protection limit values in national parks and protected landscape areas, ground-level ozone excluded, 2014
Fig. VII.5 Areas with exceeding of the ecosystems/vegetation protection limit values in national parks and protected landscape areas, including ground-level ozone, 2014
Fig. VIII.1 Development of concentrations of PM10, O3 and NO2 recalculated according to the number of urban inhabitants in 28 member states of the European Union, 2003–2012
Fig. VIII.2 Development of emissions in 28 member states of the European Union, 2003–2012
Fig. VIII.3 Annual average concentration of PM2.5 in Europe, 2012
Fig. VIII.4 Annual average concentration of benzo[a]pyrene in Europe, 2012
Fig. VIII.5 Annual average concentration of NO2 in Europe, 2012
Fig. VIII.6 The 26th highest maximum daily 8-hour average of O3 concentration in Europe, 2012
Fig. IX.1 Station networks monitoring atmospheric precipitation quality and atmospheric deposition, 2014
Fig. IX.2 Fields of annual wet deposition of sulphur (SO42- - S), 2014
Fig. IX.3 Fields of annual dry deposition of sulphur (SO2 - S), 2014
Fig. IX.4 Fields of annual total deposition of sulphur, 2014
Fig. IX.5 Fields of annual throughfall deposition of sulphur, 2014
Fig. IX.6 Fields of annual wet deposition of nitrogen (NO3- - N), 2014
Fig. IX.7 Fields of annual wet deposition of nitrogen (NH4+ - N), 2014
Fig. IX.8 Fields of annual total wet deposition of nitrogen, 2014
Fig. IX.9 Fields of annual dry deposition of nitrogen (NOx - N), 2014
Fig. IX.10 Fields of annual total deposition of nitrogen, 2014
Fig. IX.11 Fields of annual wet deposition of hydrogen ions, 2014
Fig. IX.12 Fields of annual dry deposition of hydrogen ions corresponding to SO2 and NOx deposition, 2014
Fig. IX.13 Fields of annual total deposition of hydrogen ions, 2014
Fig. IX.14 Fields of annual wet deposition of chloride ions, 2014
Fig. IX.15 Fields of annual wet deposition of lead ions, 2014
Fig. IX.16 Fields of annual dry deposition of lead, 2014
Fig. IX.17 Fields of annual wet deposition of cadmium ions, 2014
Fig. IX.18 Fields of annual dry deposition of cadmium, 2014
Fig. IX.19 Fields of annual wet deposition of nickel ions, 2014
Fig. IX.20 The development of annual deposition of sulphur (SO42- - S, SO2 - S), oxidated forms of nitrogen (NO3- - N, NOx - N) and hydrogen in the Czech republic, 1995–2014
Fig. IX.21 The development of the ratio of nitrate/sulphate concentrations in atmospheric deposition (expressed as µeq. l-1) at the CHMI stations, 1998–2014
Fig. IX.22 The development of annual wet deposition at selected stations, 1991–2014
Fig. X.1 Emissions of carbon dioxide structured by sectors, 1990–2013
Fig. X.2 Emissions of methane structured by sectors, 1990–2013
Fig. X.3 Emissions of nitrous oxide structured by sectors, 1990–2013
Fig. X.4 Emissions of F-gases, 1995–2013
Fig. X.5 Carbon dioxide emissions from the plants registered in EU ETS, 2005–2013
Fig. XI.1 Ties of the AQIS to data sources and co-operating systems, 2014
Fig. XI.2 Monitoring of basic pollutants in selected organisations – development
Fig. XII.1 Diagram showing the variogram parameters and the fitted spherical function
  Annex III
Fig. 1 Concentration wind roses expressing the dependence of average hourly concentrations of PM10 on wind direction and speed, locality Polom, 2014
Fig. 2 Seasonal concentration wind roses expressing the dependence of average hourly concentrations of PM10 on wind direction and speed, locality Polom, 2014
Fig. 3 Number of exceedances of the hourly PM10 concentration of 50 µg.m-3 depending on the time of day, locality Polom, 2014
Fig. 4 Number of exceedances of the hourly PM10 concentration of 50 µg.m-3 depending on the day of the week, locality Polom, 2014
Fig. 5 Number of exceedances of the hourly PM10 concentration of 50 µg.m-3 depending on the time of day, locality Krupka, winter period 2013/X–2014/III
Fig. 6 Number of exceedances of the hourly PM10 concentration of 50 µg.m-3 depending on the day of the week, locality Krupka, winter period 2013/X–2014/III
Fig. 7 Concentration wind roses expressing the dependence of average hourly concentrations of PM10 on wind direction and speed, locality Krupka, winter period 2013/X–2014/III
Fig. 8 Concentration wind roses expressing the dependence of average hourly concentrations of PM10 on wind direction and speed, locality Krupka, winter period 2014/X–2015/III
  Annex IV
Fig. 1 Field of the highest 24-hour concentration of PM10, 2014 (WHO)
Fig. 2 Field of the highest 24-hour concentration of PM2.5, 2014 (WHO)
Fig. 3 Field of the highest hourly concentration of NO2, 2014 (WHO)
Fig. 4 Field of the highest maximum daily 8-hour running average of ground-level ozone concentration, 2014 (WHO)
Fig. 5 Field of the highest 24-hour concentration of SO2, 2014 (WHO)