Transboundary air pollution 133
3.4. Transboundary air pollution
Transboundary air pollution (generated in one country and impacting in others) makes a Main findings major contribution to acidification and summer smog (caused by tropospheric ozone), and also to eutrophication of soil and water and dispersion of hazardous substances. The main sources of this pollution are energy use and transport in which international shipping is of growing importance. The cost-effectiveness of measures to reduce emissions from ships has been demonstrated by the European Commission in its strategy to combat acidification. However, sufficient measures are yet to be implemented.
Major emission reductions for sulphur dioxide and nitrogen dioxide adopted under the Convention on Long-Range Transboundary Air Pollution (CLRTAP) and EU legislation have reduced the harmful effects of transboundary air pollution. Projected further reductions fall short of EU targets for 2000 and 2010 and further intiatives are needed in the framework of integrated abatement strategies.
Projections for 2010 suggest that, despite the projected emission reductions, areas of the EU and (especially) the Accession Countries will continue to be affected by acid and nitrogen deposition above the level defined as the ‘critical load’. Ecosystems in the EU still receive 7% acid deposition and 39% nitrogen deposition above their critical loads. European countries where over 70% of ecosystems will still be affected by excess nitrogen deposition include the Czech Republic, Lithuania, Poland, the Slovak Republic and Switzerland.
With respect to ozone, despite the considerable efforts in precursor emission reductions, the long-term objective for protection of crops is expected to be reached only in the north-west parts of Europe (Ireland, Scandinavia). The health-related ozone threshold concentration will continue to be exceeded 50 days per year. The highest number of exceedances will be found in the more densely-populated north-western part of Europe (Netherlands, Belgium and northern France).
Moreover, despite reductions in precursor emissions, smog will remain a health threat due to increases in ozone worldwide: this calls for action on a global scale to reduce emissions of carbon dioxide, nitrogen oxides and methane.
1. Transboundary air pollution: a complex The main effects are manifested in acidifica- problem tion of water and soil, summer smog caused by tropospheric ozone, eutrophication of 1.1. It is all intertwined soils and waters, and dispersion of hazardous Transboundary air pollution is a pan-Euro- substances (see also Chapter 3.3). The pean problem, requiring pan-European environmental impacts caused by the main solutions. The main causes are emissions pollutants SO2, NOx, VOCs, ammonia (NH3) from transport and energy usage of sulphur and toxic substances are summarised in dioxide (SO2), nitrogen oxides (NOx), Table 3.4.1. volatile organic compounds (VOCs) and various toxic materials such as heavy metals Main air pollutants and their environmental impacts and persistent organic pollutants (POPs). Table 3.4.1. These pollutants (particularly carbon mon- Environmental Impact Caused by oxide (CO) and methane (CH4)) can Acidification SO NO , NH remain in the atmosphere sufficiently long 2, x 3 to be transported thousands of kilometres Eutrophication NOx, NH3 and thus to spread over the whole of Europe, Ozone VOCs, NO across national borders, far from the original x sources of polluting emissions. Bioaccumulation of toxic substances Heavy metals, POPs 134 Environmental Issues
Table 3.4.1 is of course a simplified summary, change (see Chapter 3.1) and also reduce
which abstracts from a reality of complex SO2, NOx and CO emissions, with beneficial interactions. For instance, all the acidifying impacts on acidification, tropospheric ozone compounds are precursors of particulates and urban air quality (Figure 3.4.1). which are harmful to human health, and VOC species such as benzene also have toxic 1.2. Targets and policies at European level effects and contribute to the formation of The UNECE Convention on Long-Range
harmful particulates. VOC and NOx emission Transboundary Air Pollution (CLTRAP) controls vary in their effectiveness in reducing signed in Geneva in 1979 was the first multi- ozone concentrations. As a rule of thumb, lateral treaty concerning air pollution. It has ozone concentrations in highly polluted areas provided an important demonstration that are most efficiently reduced by a combination international co-operation can achieve
of NOx and VOC controls. In regions with low results. During its first 10-15 years, the
NOx concentrations, both NOx and VOC CLRTAP resulted in protocols aiming at a
control reduces ozone levels but NOx control reduction in acidifying emissions and abate- is more effective. In parts of north-west ment of ozone concentrations. Protocols on
Europe, reductions in NOx emissions alone heavy metals and persistent organic pollutants will actually increase ozone levels, although a (1998) aim at a reduction of emissions of
reduction in NOx emissions is still desirable to these toxic materials. A second protocol on
mitigate effects of acidification and NOx and NH3 emissions is under negotiation. eutrophication and to reduce ozone forma- tion on the hemispheric and global scale. Parties to the CLRTAP were committed to a
stabilisation of NOx emissions at the 1987 Further complicating factors are the multi- level by December 1994. The VOC protocol ple environmental impacts of human activi- signed in 1991 requires emissions to be ties. Thus, for example, energy-saving either stabilised or reduced by at least 30%
measures to reduce CO2 emissions and the from the base year (usually 1988) in 1999. ensuing pollutants released mitigate climate The second Sulphur Protocol signed in 1994
Figure 3.4.1 Multi-pollutants, multi-effects
Source: EEA
CO2 CH4 N2O
Climate change CO VOCs
NOX SO2 PM NH3 NOX Fewer droughts, floods, storms, and agricultural changes etc. Urban air Eutrophication quality
Reduced losses of fish Lower emissions lead Reduced ill health biodiversity and amenity
Energy Transport
Agriculture
Household Industry CH4 VOCs NH NO SO 3 X 2 CO NOX to multiple benefits Trophospheric Acidification Ozone
Reduced damage to forests, Reduced ill health, soils, fish and buildings agricultural losses Transboundary air pollution 135
has the objective to reduce the extent by EU air emissions reduction targets Table 3.4.2. which critical loads are exceeded in Europe by 60% in the year 2000; the various coun- SO2 NOx VOCs tries are required to reduce their emissions 5EAP 35% (1985-2000) 30% (1990-2000) 30% (1990-99) by different amounts. The Protocol also has obligatory clauses regarding emissions CLRTAP 62% (1980-2000) stabilise 1987 emission 30% (1987-99) standards, including application of ‘Best levels by 1994 Available Technology’ emission standards for COM(97)88 84% (1990-2010) 55% (1990-2010) new plants. A further requirement is a (proposed targets) reduction in sulphur content to 0.2% and to Source: European Commssion, 1997; UN-ECE CLRTAP, 1998 0.05% respectively in gas oil for stationary sources and in diesel fuel for road traffic. • Integrated Pollution Prevention and EU limit, guide or target values for air Control Directive. quality concentration levels of pollutants • Implementation of measures developed including SO2, NO2 and ozone are now through the Auto-Oil Programme: being revised through so-called ‘daughter • A two-step tightening of vehicle directives’ to the Air Quality Framework emission limit values for passenger Directive (96/62/EC). cars and light commercial vehicles with the first step in the year 2000 and The EU Fifth Environmental Action Pro- the second step in 2005; gramme (5EAP) set emission targets up to • new environmental specifications for the end of the century for reduction of petrol and diesel fuels to take effect acidifying compounds and ozone precursors. from the year 2000; very low-sulphur Further targets, up to 2010, were proposed fuels to be mandatory from 2005; in the 1997 Community Strategy to combat • provision made for earlier phase-in of acidification (European Commission, 1997; very low-sulphur fuels; Table 3.4.2). This strategy emphasised the • phase-out of leaded fuels by 2000. multi-pollutant multi-effect framework and • The Solvent Directive and the Directive showed that, in terms of cost-effectiveness, to reduce emissions from storage and there is more potential for reducing sulphur distribution of petrol aim at reduction of rather than nitrogen emissions; this is VOC emissions from stationary sources because SO2 is mainly emitted from a small and at all stages of the chain of petrol number of relatively controllable large storage, distribution and usage. sources (power plants) whereas NOx is also emitted from a wide range of smaller Guided by the work done by the WHO on sources, including vehicles. human-health effects and by UNECE on effects on vegetation, the Commission has New strategies for emission abatement face proposed new ozone reference levels (Table the challenge of satisfying protection re- 3.4.3). In addition to the long-term objective quirements from all inter-related effects for the protection of human health, thresh- caused by tropospheric ozone, acidification old values to inform both the general and and eutrophication. The Commission is informed population have been defined. For currently developing an ozone-abatement the protection of human health, short-term strategy. In line with the 5EAP, the aim is to concentrations (peak values over one to address the ‘symptoms’ by setting interim eight hours) are of concern. For protection and long-term air quality objectives and the of agricultural crops and forests, ozone ‘causes’ by developing strategies and meas- concentrations integrated over the growing ures to reduce polluting emissions and also season are of importance. to stimulate changes in society’s patterns of behaviour. The new strategy will be linked with provisional national emission ceilings 2. Trends in emissions for SO2, NOx, NH3 and VOC.
2.1. Emissions of sulphur dioxide (SO2)
More specific measures for abating precur- Since 1980, SO2 emissions in Europe have sor emissions are defined in a number of EU been reduced considerably: by approximately Directives: 50% over the period 1980-1996 (Figure 3.4.2) although in comparisons between countries, • Large Combustion Plants Directive. allowance should be made for differences in • Directives on Sulphur Content of Cer- initial emission rates and economic circum- tain Liquid Fuels. stances. In the EU, the 5EAP target of 35% 136 Environmental Issues
Table 3.4.3. Ozone air quality reference levels proposed in the working EU draft Ozone Directive
Source: Europaen Concern Description Metric Value Commission, 1999b 3 Health Long Term Objective Moving 8 hours average 120 mg/m * value for the protection concentration of human health
3 Alert threshold sensitive 1 hour average 180 mg/m population concentration
3 Alert threshold general 1 hour average 240 mg/m population concentration
3 Damage to crops and Long Term Objective AOT40, May-July, 08.00- 6 000 mg/m .h** vegetation value for the protection 20.00 CET of vegetation
3 Reference level AOT40, April-September, 20 000 mg/m .h concerning visible 08.00-20.00 CET damage on forests
Ozone concentrations integrated over a certain period of time are indicated as AOTxx-values where xx is a threshold value 3 expressed in ppb (1 ppb O3 = 2 µg/m O3). The AOT40, for example, is defined as the sum of all excess concentrations above the threshold of 40 ppb (80 µg/m3). It is calculated by subtracting 80 µg/m3 from all hourly concentrations and subsequently summing all positive values.
* In addition to the Long-term Objective, a Target value has been proposed: by the year 2011 a daily eight-hour maximum of 120 mg/m3 may not be exceeded more than 20-25 times per calendar year averaged over 3 years. Current legislation (92/ 72/EC) has the limit value 110 mg/m3 average over a fixed eight -hour period.
** In addition to the Long-term Objective, a Target value has been proposed: by the year 2011 the AOT40 value may not exceed 18 000 mg/m3.h averaged over 5 years. Current legislation (92/72/EC) has the limit value 65 mg/m3 average over 24 hours.
reduction from 1985 levels by the year 2000 tion in these countries. Since 1994, the 5EAP was met in 1994. EU emissions were reduced target of 35% reduction has also been met from 19 600 ktonnes in 1985 to 10 700 by Accession Countries, as result of the ktonnes in 1995. The reduction, which will general European overfulfilment of the 30% continue, is expected to meet the commit- emission reduction objective set by the First ments of the Second Sulphur Protocol. Sulphur Protocol. At present, the relative reduction in emissions from the Accession The decrease in emissions from the Acces- Countries is similar to that in the EU, while sion Countries is most notable since 1990, their total emissions amounts to approxi- largely caused by the economic reconstruc- mately one-quarter of EU emissions.
Figure 3.4.2 Sulphur dioxide emissions were strongly reduced between 1980 and 1996 (1980 = 100%)
In general, Parties to the 160 1985 LRTAP-Sulphur Protocol (on the left) have 140 achieved a larger reduction than other countries (on the 120 right). Data officially 100 submitted is in dark colour, estimates are in light colour. 80 emissions 2 60 Source: EMEP/MSC-W, Report 1/98 % SO 40
20
0
Italy Spain France Latvia EU 15 AustriaFinlandSweden Norway Estonia Ireland Iceland Poland Greece Germany Belgium HungaryDenmark Slovenia BulgariaPortugal Lithuania Romania Switzerland Liechtenstein Luxembourg Czech Republic The NetherlandsSlovak Republic United Kingdom
CRLTAP Party to 1985 LRTAP sulphur protocol Other countries Target Party to 1985 LRTAP sulphur protocol (estimated) Other countries (estimated) Transboundary air pollution 137
2.2. Emissions of nitrogen oxides (NOx) and and 1987 for the VOC Protocol. For the year
ammonia (NH3) 1995, Accession Countries reported emis- Emission targets for nitrogen oxides set in sions well on the way to complying with the the 5EAP are far more restrictive than the VOC Protocol, while VOC emission reduc- stabilisation at 1987 levels required by the tion in the EU amounted to 11% with
First NOx Protocol of the LRTAP Conven- respect to 1990 levels and 15% with respect tion. By 1994, the average NOx emission to 1987 levels. EU emissions were reported reduction for the EEA and the Accession to be 11 500 ktonnes in 1995, that is, six Countries was 13%, thus complying with the times higher than the reported emissions commitments of the First NOx Protocol from the Accession Countries (Figure 3.4.4).
(Figure 3.4.3). However, the EU (which had Therefore, as in the case of NOx emissions, it a reduction of 11%) is unlikely to achieve is unlikely that the 5EAP VOC target emis- the 5th EAP emission target for 2000 of a sion reduction can be reached by 1999. 30% reduction; in contrast, the Accession Countries have already met this target In contrast to other pollutants, a large pro- according to the most recent official emis- portion of VOCs are emitted by natural sion estimate. processes. Biogenic VOC emission strongly depends on temperature. During ozone smog Reported ammonia emissions decreased by episodes, the natural contribution might be 14% in the EEA and the Accession Coun- as high as 60% (Slanina et al., 1998) while on tries, from 5 000 ktonnes in 1990 to 4 300 an annual basis, biogenic emission contrib- ktonnes in 1996. Again, emission reductions utes 40% of total VOC emissions over Europe in Accession Countries are considerably (Simpson et al., 1999). higher (28%) than those reported from the EU (8%). At present, there are no emission targets for ammonia, but these are expected 3. Photochemical smog to be specified in the new multi-effect multi- pollutant directives and protocols. Photochemical smog, or simply summer smog, is formed in the lowest few kilometres of the 2.3. Emissions of volatile organic compounds atmosphere. It has adverse effects on human (VOCs) health, agricultural crops, natural vegeta- The requirements for reduction of emissions tion, and materials. The main component of of non-methane volatile organic compounds smog is ozone, although levels of other (VOCs) by 30% in 1999 are different on the aggressive oxidants are elevated as well. choice of the base year: 1990 for the 5EAP There is, however, only limited information
Compared with 1987 (=100%) emissions of nitrogen oxides in 1996 show a reduction in most countries. Figure 3.4.3
Parties to the 1988 NO 200 x Protocol of the Convention 180 on LRTAP are on the left in the diagram. Other 160 countries are on the right. 140 Data officially submitted is in a dark colour, estimates are 120 in a light colour. 100 emissions Source: EMEP/MSC-W x 80 Report 1/98
% NO 60
40
20
0
Italy Spain France Latvia EU 15 Estonia SwedenAustria Finland NorwayIreland Greece Poland Iceland GermanyBulgariaSlovakiaHungary Denmark LithuaniaRomania BelgiumSlovenia Portugal Switzerland LiechtensteinLuxembourg Czech Republic UnitedThe Kingdom Netherlands
CRLTAP Party to 1988 LRTAP NOx protocol Other countries Target Party to 1988 LRTAP NOx protocol (estimated) Other countries (estimated) 138 Environmental Issues
Figure 3.4.4 Compared with 1988 (=100%) most countries have achieved the reduction in VOC emissions
Parties to the CLRTAP VOC Protocol are on the left 160 (officially submitted data in 140 dark blue, estimates in light blue). Non-parties to the 120 Protocol are on the right 100 (officially submitted data in yellow, estimates in brown). 80 60 Source: EMEP MSC-W Report 1/98 % VOC emissions 40
20
0
Italy Spain France Latvia EU 15 Austria Sweden Finland Norway Poland IrelandIceland Greece BulgariaDenmark Germany Hungary LithuaniaSlovakiaRomania Belgium SloveniaPortugal Switzerland LiechtensteinLuxembourg Czech Republic The Netherlands United Kingdom
CRLTAP Party to 1988 LRTAP VOC protocol Other countries Target Party to 1988 LRTAP VOC protocol (estimated) Other countries (estimated)
available on concentrations and effects of the ozone situation during the relevant these other oxidants. As no significant effects growing season. The AOT is a practical have been observed at current ambient indicator for ozone effects on vegetation. It levels, no international guidelines have been must be realised, however, that it is only a set for the other photochemical oxidants first, crude estimate of the real ozone expo- found in summer smog. sure of vegetation. Due to its simplifications, the link between AOT and actual vegetation Ozone and its precursors have an atmos- damage might be weak. pheric residence time of several days or more. Under average summer conditions, air First of all, the AOT gives a potential but not pollutants are transported over distances of an actual exposure of vegetation. Under dry 400-500 km per day. Besides the and hot conditions, the plant protects itself transboundary character, summer smog may by closing its stomata. Although ozone show a more local character. For example, in concentrations are likely to be high under the Mediterranean Basin, air masses re- these conditions, the closed stomata prevent entering the source regions have been uptake of ozone and the damaging effects of shown to raise pollution levels (Millan et al., ozone will be small. In the AOT concept this 1997). can be included by adding a constraint on relative humidity. This makes it, however, High levels of ozone occur during short more complex and less transparent. periods of two to four days. Threshold values set for the protection of human health are In the newly proposed daughter directive on exceeded regularly over large parts of ozone, the integration time of AOT is clearly Europe. Smog episodes are often found defined: May to July using all one-hourly during summer over most parts of the values measured between 8 AM and 8 PM continent, during periods with clear skies, CET. This period may differ from the active increased solar radiation and elevated period of the plants. Daylight hours, defined temperatures (Map 3.4.1). The occurrence as solar radiation above a certain minimum and duration of these episodes varies might be more appropriate. Also the grow- strongly from one year to the next. ing season varies all over Europe and in places extends beyond the three months 3.1. Accumulated exposure specified in the directive. Based on a series of controlled exposure experiments, the concept of AOT40 (accu- The simple and clear definition of AOT mulated ozone hourly concentrations above suggests that monitoring will be easy. Unfor- 80 µg/m3) is chosen as an indicator for tunately, there are a number of complicating exposure of ecosystems. The great advantage factors which make the observed AOT value of the AOT concept is that it is indicative of sensitive to monitoring conditions: Transboundary air pollution 139
• the measuring height: monitoring ozone 30˚ 20˚ 10˚ 0˚ 10˚ 20˚ 30˚ 40˚ 50˚ 60˚ at a height of 1 m (crops) or at 10 m (at A r cti c O c ean Mean of daily crown level of trees) might result in a summer maximum 60˚ concentration of ozone factor of 2-3 difference in AOT; • missing data will lead to systematic 0 1000 km 60˚ underestimation of the AOT; an agreed n Exceedance in µg/m³ correction method will be required. of the threshold 120 µg/m³,
Ocea accumulated hourly values N orth in the EMEP 150 – grid For practical reasons, the time resolution S ea 50˚ more than 104 applied in the current atmospheric models is 50˚ ntic 92 – 104 e l a n n la h 80–92 six hours, which is too coarse to calculate an C 68–80 At AOT without further assumption on the a Se less than 68 diurnal variation of ozone. This problem will Black 40˚ Modelled from 1990 level emissions. be solved in the next generation of models. Meteorology from selected years. Notwithstanding these drawbacks, the 40˚ AOT40 is, according to current knowledge, M e d i Map 3.4.1 t e r The model indicates a clear the best indicator for vegetation exposure. r a a n e a n S e gradient over Europe: 30˚ summertime concentrations 3.2. Threshold values for ozone are exceeded 3 30˚ 0˚ 10˚ 20˚ 30˚ ranging from 60 mg/m in All EU threshold values set for ozone under the northern part to more the current Ozone Directive (92/72/EC) than 100 mg/m3 in the central part and in the have been exceeded since 1994, the year the Mediterranean region (1 ppb 3 Directive came into force. Thresholds set for of arable land is exposed to exceedance of O3 » 2 mg/m ). the protection of human health and vegeta- this WHO guideline. Source: Simpson et al., 1997 tion are exceeded in all Member States every year. Short-term thresholds for protection of For protection of forests, the WHO and vegetation and the threshold values for CLRTAP have set a guideline/critical level of public information are exceeded in most AOT40, 24 hours, April-September of 20.000 Member States. The threshold concentration µg/m3.h. Both monitoring and modelled for warning the population is exceeded only data indicate that Scandinavia, Ireland and occasionally (Beck et al., 1998). the UK are below the critical level most years. In the rest of Europe, the level is One of the 5EAP targets is that air quality exceeded by up to a factor of three. Calcula- guidelines recommended by the WHO tions indicate that about 35% of Europe’s should be mandatory by 1998. Routine monitoring (Hjellbrekke, 1997; de Leeuw and de Paus, 1998) indicates that the WHO 30˚ 20˚ 10˚ 0˚ 10˚ 20˚ 30˚ 40˚ 50˚ 60˚ value of 120 µg/m3 eight-hour average is A r cti c O c ean Accumulated excess exceeded in all EU Member States and in all of ozone concentration 60˚ other European states which report data. 0 1000 km Model calculations, allowing for estimation 60˚ of exceedance in the whole of the European n Concentration in µg/m³/h exceeding the threshold territory (Map 3.4.2) indicate that 99% of of 120 µg/m³/h in the EMEP 150 – grid EU inhabitants are exposed to at least one Ocea N orth exceedance per year. For the development of S ea 50˚ more than 12 000 abatement strategies, the AOT60 (accumu- 50˚ ntic
3 n e l a n 6000–12000 lated excess above 120 µg/m ) has been la C h
At taken as indicative of ozone health impacts. a Se Black 2 000 – 6 000 According to WHO recommendations, the 40˚ 40˚ AOT40 for daylight hours in May-July should 200 – 2 000 not exceed 6 000 µg/m3.h for the protection less than 200 M e d i t e areas with of natural vegetation and the prevention of r r a n e a no exceedance more than 5% crop yield loss (this is also the e a n S 30˚ Modelled from 1990 level emissions. critical level for ozone protection of crops Meteorology from selected years. 30˚ 0˚ 10˚ 20˚ 30˚ under CLRTAP). According to observations, this AOT40 parameter exceeds 6 000 µg/ Map 3.4.2 m3.h in most of the EU, with the exception Almost the entire population of Europe is exposed to ozone levels exceeding the WHO of northern parts of both Scandinavia and guideline for protection of human health. This map shows the average accumulated excess of ozone concentration above a level of 60 ppb (=120 mg/m3) modelled over five years. the UK (Hjellbrekke, 1997). Modelled results indicate that, averaged over five years, 94% Source: Simpson et al., 1997 140 Environmental Issues
coniferous forests and 70% of broadleaf Distribution of ozone concentrations over forests experience exceedances. Europe also differs considerably from year to year. While the mean daily maximum value is 3.3. Ozone levels vary from year to year and over highest in Italy and France, exceeding 104 Europe µg/m3 (see Map 3.4.1), the AOT60 is highest Ozone concentrations, particularly peak in northern France, Belgium and south values, vary considerably from year to year western Germany (see Map 3.4.2). due to specific meteorological conditions, whose occurrence is very variable in time Average ozone concentration in summer and space (Figure 3.4.5). Typical variations shows an increase from north-west to central from year to year for peak concentrations Europe. In mountainous regions, average (98 percentile) are 10-15%, while AOT40 ozone concentrations are higher than in may show variations of about a factor of lowland plains. There are indications, still to three. be confirmed over the long-term, that peak ozone levels are higher in southern Europe than in the north. Characteristics of ozone formation and transport in major Mediterra- Figure 3.4.5 Threshold values defined in the EU Ozone Directive (92/72/EC) are exceeded frequently and widely nean cities and coastal areas differ from those normally occurring in northern continental areas (Millan et al., 1997). This figure shows the number of days as a function of the minimum number of Exceedance of threshold 65 ug/m3 (24h) 3.4. Present trends in ozone are small, and hard Member States where at to detect least one exceedance of a 365 In the late 1990s, rural ozone levels are three threshold value was observed in 1997 (e.g. on 300 times higher than in the pre-industrial era. 174 days the threshold value Around the year 1880, average ozone levels of 110 mg/m3 was exceeded 200 at a rural site near Paris were about 20 µg/ in at least four Member 3 States). Note: information m , but by 1950, rural ozone levels had 3 3 on exceedances of 65 mg/ Number of days 100 increased to 30-40 µg/m , and to 60 µg/m m3 and 110 mg/m3 were around 1980. However, trends in rural ozone submitted by 14 Member 0 States only. in the last decade are statistically insignifi- 13579111315 cant (Beck et al., 1998). Studies are Source: de Leeuw and de Number of Member States underway to try to explain these trends from Paus, 1998 the analysis of the trends in the emissions of ozone precursors (Lindskog et al., 1998). Exceedance of threshold 180 ug/m3 (1h) 200 Trends in ozone episodes are even more difficult to assess because of annual variabil- 150 ity of peak ozone concentrations (Figure 3.4.6). A recent analysis of peak ozone data 100 submitted under the Ozone Directive (de Leeuw et al., 1997) showed for 68 stations
Number of days 50 over the period 1989-1997 a significant upward trend at only two stations and a 0 downward trend at 22 stations. For the 13579111315 majority of the 68 stations analysed, no Number of Member States significant trend was detected.
A detailed analysis of ozone data in the UK Exceedance of threshold 110 ug/m3 (8h) (PORG, 1997) showed a decrease in peak ozone levels. The hourly maximum ozone 300 concentrations, averaged per month over the period 1986-1995, are 40-60 µg/m3 below 200 that during the period 1972-1985. At nine out of 16 rural stations, there is however a 100 significant positive trend in annual mean
Number of days concentrations.
0 13579111315 Urban ozone showed downward trends in Number of Member States Central London between 1973 and 1992, while monthly means increased by 15% per Transboundary air pollution 141
year at a suburban station in Athens in the Ozone concentrations differ widely between Figure 3.4.6 period 1984-1989. monitoring stations
Ozone concentrations in ‘unpolluted’ air The reason for this masses arriving over the North Atlantic Median concentrations of ozone (50 percentile) difference is the local impact of NO sources: in urban region at the Irish station Mace Head ap- x 80 areas and especially in peared to increase over the 1990-1996 streets the locally emitted 3 period with 0.18 µg/m per year equivalent 60 traffic emissions result in a to 0.2% per year (PORG, 1997). Model temporary reduction of )
3 ozone levels. Further calculations on a global scale support the 40 downwind, ozone levels will findings of an ongoing change in chemical (ug/m resume previous high levels. composition of tropospheric background air 20 Source: de Leeuw et al., (Parrish et al., 1993; Collins et al., 1998; 1997 Berntsen et al., 1997; Hov and Flatøy, 1997). 0 Current daily mean concentrations of ozone 1989 1991 1993 1995 1997 are three to four times higher than in the Eupen (BE) Bottesford (GB) Mont St. Nicolas (LU) Wijnandsrade (NL) pre-industrial era mainly as a result of the Utrecht (NL) considerable growth in NOx emissions from industry and the transport sector. Peak concentrations of ozone (98 percentile) 180 4. Acidification 160 4.1. Critical loads ) 140 Acid deposition originates largely from man- 3
made emissions of sulphur dioxide (SO2), (ug/m 120 nitrogen oxides (NOx) and ammonia (NH3). Major sources of these pollutants are the 100 usage of fossil fuels for power generation, 80 transport and agricultural practice. Deposi- 1989 1991 1993 1995 1997 tion of these three primary components and Eupen (BE) Great Dun Fell (GB) Mont St. Nicolas (LU) Vredepeel (NL) their secondary-reaction products leads to Zegveld (NL) acidification (sulphur and nitrogen deposi- tion) and euthrophication (nitrogen deposi- tion). Acidification is causing damage to freshwater systems, forest soils and natural concept of ‘critical load’, defined as the ecosystems in large areas of Europe. The highest deposition of chemical compounds effects of acidification have been evident in that will not cause long-term harmful effects various different ways, including defoliation on the ecosystem structure and function, in and reduced vitality of trees, declining fish order to target emission reductions towards stocks and decreased diversity in acid-sensitive the actual damage. The critical load depends lakes, rivers and streams and changes in soil on characteristics of the soil and ecosystem chemistry. Nitrogen contributes also to the and varies strongly over Europe. Lake systems eutrophication of terrestrial and marine in Scandinavia are very sensitive (low critical ecosystems and it is an important precursor of load) whereas the Iberian Peninsula is less ground-level ozone. Along with these effects sensitive – partly because the deposition of on ecosystems, there are also corrosion effects base cations (e.g. Sahara dust) neutralises the on materials, cultural monuments and acid deposition to some extent. buildings. In addition, there is growing concern about the adverse health effects The effects of acidification on forests and related to secondary-reaction products of freshwater ecosystems and the effects of acidifying and eutrophying pollutants. eutrophication on terrestrial ecosystems are included in the present definition of critical Since the signature of the 1979 LRTAP loads. Other effects, such as corrosion Convention, significant reductions in harmful damage to monuments, eutrophication of emissions have been achieved. Increasing marine ecosystems, or health effects, are not attention is now being given to the analysis of included within the critical load approach. effects of emissions, in order to differentiate The new strategies for emission reduction reduction commitments according to the face the challenge of satisfying protection varying sensitivity of the natural environment. requirements from all these inter-related There is now an increasing focus on the effects. 142 Environmental Issues
30˚ 20˚ 10˚ 0˚ 10˚ 20˚ 30˚ 40˚ 50˚ 60˚ 4.2. Exceedances of critical loads Exceedance A r cti c O c ean Sulphur and nitrogen deposition combined of critical loads contributes to exceedance of critical loads for sulphur in 1996 60˚ (Maps 3.4.3, 3.4.4, and 3.4.5; excess deposi- 0 1000 km tion was calculated as the percentage of 60˚ Loads in eq/ha n ecosystems in each grid with acid deposition in the EMEP 150 – grid above the critical loads, for scenario calcula- more than 2 000 Ocea tions in preparation for the Second CLRTAP N orth S ea 50˚ Sulphur Protocol. The excess deposition
50˚ ntic over the fifth percentile was used as the main 1 000 – 2 000 e l a n n la C h criterion driving emission reductions.)
At a Se Black Pollution ‘hot spots’ can be identified, such 40˚ 400 – 1 000 as the so-called Black Triangle (Box 3.4.1). 40˚ Exceedances of critical loads of acidification 200 – 400 and eutrophication over Europe are at M e d i t e 40 – 200 r r a a present mostly dominated by nitrogen less than 40 n e S e a n deposition, the relative importance of which areas with 30˚ no exceedance is increasing, showing the need for a new 30˚ 0˚ 10˚ 20˚ 30˚ nitrogen protocol. There are different ways to determine critical loads and their 30˚ 20˚ 10˚ 0˚ 10˚ 20˚ 30˚ 40˚ 50˚ 60˚ exceedances, because the amount of nitro- Exceedance A r cti c O c ean of critical loads gen deposition that an ecosystem may for eutrophying 60˚ tolerate without harmful effects also depends nitrogen in 1996 on the level of the sulphur deposition and 0 1000 km 60˚ vice versa. The critical load function for each n separate ecosystem can be approximated Loads in eq/ha taking account of sulphur deposition, in the EMEP 150 – grid Ocea N orth S ea 50˚ acidifying nitrogen and eutrofying nitrogen. Exceedances are recorded for each particu- 50˚ ntic more than 1 000 lar ecosystem whenever the actual deposi- e l a n n la C h tions fall outside the function. At a Se Black 40˚ In preparation for the EU acidification 400 – 1 000 40˚ strategy, an ‘area of exceedance’ (AE) concept was developed for scenario analysis. 200 – 400 M e d i t e The alternative way to calculate exceedances 40 – 200 r r a a less than 40 n e a n S e was to consider the area occupied by the areas with 30˚ ecosystems, rather than the number of no exceedance 30˚ 0˚ 10˚ 20˚ 30˚ ecosystems with depositions exceeding their critical loads.
30˚ 20˚ 10˚ 0˚ 10˚ 20˚ 30˚ 40˚ 50˚ 60˚ Exceedance A r cti c O c ean Recently, a further refined measure for of critical loads evaluating ecosystem protection has been for acidifying nitrogen 60˚ in 1996 developed. The so-called ‘average accumu- lated exceedance’ (AAE) actually calculates 0 1000 km 60˚ n the exceedance of critical loads for all ecosystems in a given grid cell (Posch et al., Loads in eq/ha in the EMEP 150 – grid Ocea 1997). Exceedances of individual critical N orth S ea 50˚ loads are added for all ecosystems and
50˚ ntic averaged in terms of the area covered by more than 1 000 e l a n n la C h each individual ecosystem in the grid cell.
At a Se Black 40˚ 400 – 1 000 40˚ Map 3.4.3 200 – 400 M e d i t e 40 – 200 r Map 3.4.4 r a a less than 40 n e a n S e areas with 30˚ Map 3.4.5 no exceedance 30˚ 0˚ 10˚ 20˚ 30˚ Source: EMEP Transboundary air pollution 143
Box 3.4.1. Air pollution in the Black Triangle Time courses of total annual emissions and air Figure 3.4.7 On a Europe-wide scale, problems with acidifica- pollution by sulphur dioxide in the Black Triangle tion are most serious within the Black Triangle. Exceedances of critical loads show their European maximum over this area and they are primarily Annual emissions Air pollution concentration related to sulphur deposition, despite effective reductions in past years. The brown coal belt, which Czech part of Black Triangle Czech Republic forms the heart of the Black Triangle, stretches from German part of Black Triangle Germany Poland Lower Silesia (Poland) to Southern Saxony Polish part of Black Triangle (Germany) and Northern Bohemia (the Czech 1600 Republic). It covers a mountainous area with 6.4 3 1400 140 million inhabitants. Climate, soils, geomorphology, and geology vary substantially. Poor and acid soils 1200 120 are common and low levels of critical loads of sulphur characterise these areas. 1000 100 800 80 The long-term annual precipitation totals are in a range of 500 mm in the basin to 1 350 mm at 600 60 higher altitudes. Annually, there are more than 50 400 40 days of continuous fog and 70% of the days are cloudy. Situations of stagnant air often occur during 200 20 winter, causing accumulations and the highest Annual emissions / ktonnes 0 0 Air pollution concentration / ug/m concentrations of air pollutants. 1989 1990 1991 1992 1993 1994 1995 1996
The intensive exploitation of lignite began in the 19th century and the development of mining, heavy and chemical industry intensified after World War II. for emissions and air pollution. However, the Source: PHARE Topic link - The most dense concentration of large emission deposition of sulphur and other acidifying substances ETC/AQ sources in the Black Triangle region is in industrial in the Black Triangle area is still fairly high (Map 3.4.6). areas of Most, Chomutov and Ústí nad Labem in Sulphur deposition is expected to further decline from the Czech Republic and Zwickau, Chemnitz, about 9 g/m2/year in 1990 to 1 g/m2/year in 2010. Dresden, Plauen and Elsterber in Germany. The long-term exceedances of critical loads by Between 1989 and 1996, the air emissions from the atmospheric deposition of sulphur are highest on top largest Black Triangle sources were reduced of the mountains. These are the areas with the worst significantly (Figure 3.4.7). Sulphur dioxide forest damage. During the period 1972-1989, about emissions were reduced by 50% in Poland and the 50% of the coniferous forests in the Ore Mountains Czech Republic and to 30% in Germany. The disappeared. The most affected areas were on slopes nitrogen oxides emissions also decreased by 50% in facing south and south-east. The absolute the Czech Republic and Germany. The improve- deforestation rate decreased from 26.7 km2/year in ment of air quality in the Black Triangle region is the beginning of the period to 7.8 km2/year in 1989. the result of emission abatement of German and Only 26% of the Bohemian forest, 45% of the Czech sources, as well as the reconstruction of Saxonian forest, and 22% of the Silesian forest Turów Power Plant in Poland. There is also a remains undamaged (Hlobil and Holub, 1997). Air remarkable decrease of coal consumption by small pollution has changed the ecosystem in North sources and households, due to substitution with Bohemia, which resulted in soil acidification, loss of gas and other types of fuel. base cations, changes in plant community composition and forest damage. Deforestation Concentrations of sulphate and nitrates in negatively influences availability and quality of water precipitation show decreasing trends similar to those and soil erosion.
12˚ 13˚ 14˚ 15˚ 16˚ 17˚ Cottbus Deposition of sulphur GERMANY in the Black Triangle, POLAND 1997 Halle 0 50 km Leipzig
border of Black S Wroc aw Triangle Dresden y i 51˚ l Loads in eqH/ha/yr n 51˚ Gera Chemnitz e more than 3 000 o s Zwickau Wa brzych 2 000 – 3 000 x Ústí nad Dêcín i Labem Liberec a a 1 500 – 2 000 Most Trutnov 1 000 – 1 500 S 750 – 1 000 Karlovy m i a 500 – 750 Vary e Hradec less than 500 h Králové o Prague B Pardubice 50˚ 50˚ Map 3.4.6 The demarcation is that of Plzen CZECH REPUBLIC the EU PHARE-funded Black 12˚ 13˚ 14˚ 15˚ 16˚ 17˚ Triangle Project Source: Phare Topic Link/AQ