The weekend effect
Why is it that when pollution emissions fall, ozone levels often
rise, asks Peter Borrell. It's an issue that bedevils European air
quality policy-makers
At weekends, during much of the summer in North-western Europe,
the concentration of ozone (O3) in
the boundary layer (the lowest km or so of the atmosphere) rises
appreciably above its general weekday value. This is despite the
fact that emissions of its chemical precursors - from car exhaust
fumes and industrial smoke - diminish. This 'weekend effect'
indicates the complexity of photo-oxidant formation in the
troposphere (approximately the lowest 15km of the atmosphere). It
also highlights the difficult task facing the would-be European
policy-maker seeking to reduce the concentrations of air pollutants.
Ozone occurs naturally in the troposphere as a product of the
sunlight-induced photo-oxidation of methane, carbon monoxide and
volatile organic hydrocarbons (VOCs), in the presence of nitrogen
oxides (NOx), (see
Box). Some is also brought down from the stratosphere by
vigorous frontal systems and convective storms, or (much more
slowly) by diffusion.
Pre-industrial background levels of tropospheric ozone are
thought to have been less than 40µg m-3. This figure has doubled in the past
century to between 60 and 80µg m-3. Much higher concentrations can be
found in the summer smog episodes that often attend periods of
static high pressure, with ozone concentrations reaching 300µg m-3 or more in some areas. Such
concentrations lead to ozone exposures in excess of the eight-hour
average concentration of 120µg m-3
recommended by the World Health Organisation (WHO) to protect human
health.
These photo-oxidant problems are not confined to Europe: summer
smog was first recognised as a problem in the Los Angeles basin in
the 1950s and the US has a long history of trying to cope with the
problem at both state and federal levels. The problem is also
endemic in many conurbations in developing countries where emissions
from industry and heavy traffic combine with tropical sunlight to
produce high concentrations of ozone and other photo-oxidants.
Various experiments, mostly in Germany, have looked at the
effects of short-term emission reduction on ozone concentrations. In
one case, traffic in and around the city of Heilbronn was
drastically curtailed for a summer weekend. Hardly any reduction in
ozone was observed, and the conclusion from all such studies is that
temporary ozone abatement measures are not effective in small areas.
In other words, regional rather than local measures are required to
reduce ozone, though even the strongest regional abatement measures
have only a small effect on peak episode concentrations.
Summer weekends bring a reduction of some 20 to 30 per cent in
industrial and vehicle emissions compared with weekdays. Figure
1 shows the daily summer averages for ozone exposures in
Belgium. Despite the known weekend decrease in emissions, average
ozone exposures increased at weekends for rural, suburban and urban
sites. The effect is well documented; data from European urban
background stations indicate that ozone concentrations on weekend
days in summer are, on average, 10 per cent higher than on working
days while emissions are estimated to be lower by 30 per cent or
more. Similar effects are seen in California.
|
Fig 1. The 'weekend
effect' can readily be seen in these daily AOT60 exposure
index values for Belgium averaged between 1987 and
1996 (Gerwin Dumont, VMM, Belgium)
|
But another case shows the varied nature of the problem: in the
neighbourhood of Vienna, Austria, ozone levels remain about the same
throughout the week in the summer months; there is no weekend
effect.
European policy development must take account of regions with
differing climates and population densities. Also, while some of the
problems appear to be local to individual cities or small regions,
air movements during episodes of stagnant high pressure can
transport ozone and other pollutants over hundreds of km, so that a
consistent policy is required for the whole continent.
Tropospheric ozone |
Tropospheric ozone may
either be formed by photochemical oxidation, as
indicated below, or it may be brought down from the
stratosphere to the troposphere by vertical atmospheric
mixing, usually in vigorous frontal systems or severe
convective storms.
The photo-oxidation of
organic compounds occurs through a series of reactions
usually initiated by the hydroxyl radical, the principal
agent of attack on trace substances in the atmosphere.
As an example, consider the oxidation of CH4. The initial attack by
hydroxyl radical forms a methyl radical which in turn
reacts with O2 to give
a methyl peroxy radical: |
CH4 + HO• |
→ |
•CH3 + H2O |
(1)
|
•CH3 + O2 |
→ |
CH3O2• |
(2)
|
In a continental atmosphere
during the day, CH3O2• will probably
react with NO to form a methoxy radical, which in turn
reacts with O2 to form
formaldehyde, HCHO, and a hydroperoxy radical. This
reacts with further NO, forming NO2 and regenerating an
HO• radical: |
CH3O2• + NO |
→ |
CH3O• + NO2 |
(3)
|
CH3O• + O2 |
→ |
HCHO + HO2• |
(4)
|
HO2• + NO |
→ |
HO• + NO2 |
(5)
|
The reaction sequence
(1) to (5) constitutes a chain
reaction with HO• as the chain carrier.
During the day, the NO2 formed in reactions
(3) and (5) can be photolysed, forming
an oxygen atom that adds to O2 to form ozone,
regenerating NO in the process: |
NO2 + λ (400 nm) |
→ |
NO + O |
(6)
|
O + O2 |
→ |
O3 |
(7)
|
Reactions (6) and
(7) can be reversed by the rapid reaction of NO
with ozone: |
NO + O3 |
→ |
NO2 + O2 |
(8)
|
Reactions (6) to
(8), with their dependence on the concentration
of NOx ([NO]
+ [NO2]) and the light
intensity, determine the local concentration of ozone.
Overall, the oxidation of methane, CO and VOCs in the
continental boundary layer in summer under anticyclonic
conditions generates ozone, provided enough NOx is present.
The OH/HO2
chain is terminated by removal of hydroperoxy radicals
in reactions such as: |
HO2• + HO2• + M |
→ |
H2O2 + O2 + M |
(9)
|
while hydroxyl radicals and
NO2 are removed by
reactions such as: |
HO• + NO2 + M |
→ |
HNO3 + M |
(10) |
The chain lengths of both
series (OH/HO2 and
NO/NO2) are short and
the formation of ozone relies on a continuing supply of
precursors. | |
Why non-linearity?
From a chemical point of view, the source of ozone's 'non-linear'
behaviour lies in the sequence of reactions by which it is formed
(see Box). In a polluted atmosphere, VOC is oxidised to a
carbonyl compound; hydroxyl (OH) and hydroperoxy (HO2) free radicals are consumed, but then
regenerated in a short chain reaction; and NO is converted to NO2. The photolysis of NO2 by sunlight leads directly to ozone
formation, regenerating NO in the process.
|
Fig 2. The change in
NOx and ozone
concentrations in a parcel of air passing over a source region
from left to right |
Figure 2 illustrates the effects of these processes on a
parcel of air passing over a city. The principal source of emissions
is in the city centre, where NOx concentrations are high. The
ozone concentration is kept low by the reaction with NO in the
so-called 'titration reaction'.
NO + O3 → NO2 + O2
Also, in NOx-rich
areas, some of the hydroxyl radicals, which would otherwise
contribute to VOC oxidation and ozone production, are consumed by
reacting with NO2 to form HNO3.
Away from the town centre, the NOx concentration diminishes (it
is lost to the ground or reacts with alkyl radicals to form other
nitrogen compounds); the excess NO2 is photolysed; and the ozone
concentration increases. In this way, surrounding suburbs and rural
areas are generally subjected to higher ozone exposures than city
centres.
Scientists have attempted to characterise local regions as
'NOx-limited' and
'VOC-limited' with respect to the reduction of photo-oxidant
formation. The regime in a particular region will depend principally
on the concentration of NOx and the VOC/NOx ratio. In a city centre for
example, where NOx
concentrations are high, a reduction in VOC is likely to be more
effective in reducing photo-oxidant concentrations than cutting
NOx, and the centre is
said to be 'VOC-limited'. Conversely in the surrounding countryside,
where the NOx
concentration is much lower (Fig 2), cutting NOx emissions is likely to be
more effective than reducing VOC emissions; it is thus 'NOx-limited'.
The formation of photo-oxidants in general, and of ozone in
particular, is therefore a highly non-linear process with the rates
of formation depending on the concentrations of precursors in
complex ways. The general weekend effect apparently indicates a
VOC-limited regime with an excess of NO2 keeping the ozone formation low on
weekdays via the titration reaction. At weekends, when emissions are
reduced, the NOx falls
and the O3 concentration rises.
A lot of work has attempted to characterise particular regions
experimentally as NOx- or
VOC-limited, although this will vary with time and weather. Might
one way to characterise such areas simply be to look for a positive
weekend signal in ozone concentrations?
Policy development
On a European scale the effect of non-linearity is shown in
Fig 3 produced by model calculations made for EMEP, the
cooperative programme for evaluating and monitoring the long-range
transmission of air pollutants in Europe. It shows that, over most
of the continent, the reduction of NOx concentrations by 50 per
cent would reduce ozone concentrations, although usually by less
than 50 per cent. However, the green region (Fig 3) over
North-western Europe indicates that such a reduction would lead to
an increase in ozone exposure.
|
Fig 3. Percentage
reductions in the modelled mean of daily maximum ozone values
for the summer months in Europe (David
Simpson, EMEP; IVL, Göteborg. Reprinted with permission from
AGU, J. Geophys. Res., 1995, 100,
22891) |
The unexpected effects of non-linearity are mainly associated
with high NOx
concentrations and these occur in most city centres and, as Fig
4 clearly shows, generally in North-western Europe and in the
Po Valley in Italy. These data for NO2 were obtained from satellite
measurements and illustrate the potential power of satellite data
for monitoring tropospheric pollution in the future.
|
Fig 4. Tropospheric
column densities of NO2 in
the summer of 1997 obtained from GOME data on the ERS-2
satellite (Andreas Richter and John Burrows,
IUP, Bremen) |
Policy-makers taking into account the effects of non-linearity
need to consider the following:
- reductions in VOC and NOx emissions will not produce
proportionate decreases in ozone exposures;
- small or moderate decreases in NOx may actually increase
ozone concentrations and exposures in regions of high pollution;
- in the long term it will be necessary to reduce both NOx and VOC appreciably to
secure worthwhile reductions in ozone;
- in the short term it may be necessary to identify regions as
NOx- or VOC-limited in
order to maximise the cost effectiveness of strategies;
- measures that offer benefits at the regional or European scale
may be locally counter-productive; and
- different strategies will probably be necessary for different
geographical regions and perhaps for different regions within one
country.
This last point was unfortunately not fully appreciated in the
early US attempts to extend the experience from Los Angeles (largely
VOC-limited) to areas with appreciable natural VOC concentrations
(leading to an NOx-limited regime). Measures to
limit VOC emissions in such areas produced little or no effect on
ozone pollution.
The first international effort to curb air pollution in Europe as
a whole was the 1983 Convention on Long Range Transboundary Air
Pollution (CLRTAP) produced under the auspices of the UN Economic
Commission for Europe, of which EMEP is the monitoring arm. The
convention concentrates on the reduction of emissions and now has
protocols for reducing sulfur, nitrogen oxides, VOCs, ammonia and
heavy metals. One outcome has been the large reduction in the
emission of sulfur dioxide in Western Europe over the past 15 years;
it is to be hoped that the newer protocols will be equally
effective.
The approach adopted by the European Union in its own clean air
'framework' directive, and in the ozone daughter directive, is to
set a limit value for exposure for a particular component; to set
time schedules for the countries to reduce exposures below the limit
value; and to require the countries to report exceedances and the
measures being taken to reduce them below the limit value.
Ozone poses particular problems in this respect. Not only is it a
secondary pollutant with a non-linear response to precursor emission
reductions, but the measures required to reduce emissions will be
increasingly costly. In recognition of these problems, the EU 1999
position paper proposed setting a two level objective for ozone:
- a long-term objective, based on the WHO value for exposure;
and
- a target value to serve as an interim objective.
This two step approach recognises the impracticability of
reaching the long-term objective in the foreseeable future; in the
meantime, the target value with somewhat less stringent requirements
will set practical goals for the immediate future.
The new EU ozone directive follows the WHO guidelines and deals
with summer smog by setting a limit for the maximum eight-hour
average concentration for ozone of 120µg m-3 (ca 60ppb).
The directive also deals with a second facet of the ozone
problem; that of low level continuous exposure to ozone, which is
known to affect vegetation and crop growth. Exposure is expressed in
terms of an index, AOT40, which is the product of the exposure time
in hours and the ozone concentration above a threshold of 40ppb
(ca 80µg m-3). The limit
set by the directive is 3ppm hours (6000µg m-3 hours).
Unfortunately, measurements appear to show that the ozone
concentrations arriving at the western edge of Europe in summer are
between 60 and 80µg m-3 (30 and
40ppb mixing ratio) and may be increasing. Clearly such levels make
it questionable whether it will ever be possible to conform to the
directive's long-term vegetation-related objective.
EU National Emission Ceilings address the measures necessary to
meet the target and long-term values. This imposes emission ceilings
for SO2, NOx, VOCs and NH3, to meet the interim targets for
ozone, and takes into account the effects of non-linearity. It is
now the business of the countries to implement the necessary
regulations and confront the potential economic and political
problems. The EU has emphasised the general nature of air pollution
and is developing an ongoing review and legislative process in the
CAFE (Clean Air for Europe) initiative.
Taken as a whole, the efforts being made should help to contain
the problems for the next few years but the complexities involved in
the troposphere in general, and ozone in particular, will make for
interesting challenges in the new century.
Peter Borrell, with his wife Patricia, runs P&PMB
Consultants, Newcastle-under-Lyme, Staffordshire ST5 2QJ; e-mail: pborrell@luna.co.uk
Acknowledgements: Thanks to Bill Sturgess (UEA, Norwich)
for encouraging me to write this article, Markus Amann (IIASA,
Austria), David Simpson (IVL, Göteberg; EMEP) and Patricia Borrell
for commenting on the manuscript, and Gerwin Dumont (VMM, Belgium),
David Simpson (IVL, Göteborg), John Burrows and Andreas Richter
(IUP, Bremen) for supplying information and figures.
Further reading
- P. Bruckmann and W. Wichmann-Fiebig, The weekend effect
and ozone in Europe, EUROTRAC newsletter no.19,
2-9, 1997.
- M. Roemer, Trends of ozone and precursors in
Europe, TNO report R2001/244. Apeldoorn, The Netherlands,
2001.
- S. Reis et al, Atmos. Environ., 2000,
34, 4701.
- A. Neftel and T. Staffelbach, Proc. EUROTRAC symposium
'98, Vol 2, p656, (eds. P. M. Borrell and P. Borrell).
Boston & Southampton: WIT Press, 1999.
- National Research Council, Rethinking the ozone problem
in urban and regional air pollution. Washington, DC:
National Academic Press, 1999.
- European Union, Ozone Position Paper, EU, Luxembourg, 1999.
- European Union Air Quality: www.europa.eu.int/comm/environment/air/background.htm
- The Clean Air for Europe Programme: www.europa.eu.int/comm/environment/air/cafe.htm
- UN-ECE Convention on Long Range Transboundary Air Pollution:
www.unece.org/env/lrtap/multi_h1.htm
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