Emissions Scenarios - IPCC
Emissions Scenarios - IPCC
Emissions Scenarios - IPCC
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Scenario Driving Forces 153<br />
Nakicenovic, 1996; McDonald, 1999; Riahi and RoeM, 2000),<br />
which are linked with the acidification model RAINS for<br />
Europe and Asia, or the AIM (Morita et al., 1994) model for<br />
Asia. These models extend earlier energy sector models that<br />
dealt with a comparative costs assessment of isolated sulfur<br />
and carbon reductions and joint mitigation, such as the OECD<br />
GREEN model (Complainville and Martins, 1994) or the<br />
IIASA MESSAGE model (Grübler, 1998b; Nakicenovic et al,<br />
1998a). The state of knowledge and availability of models to<br />
study the joint benefits of sulfur and carbon emission<br />
reductions was reviewed in the 1995 <strong>IPCC</strong> SAR WGIII Report<br />
(Bruce et ai, 1996) and is expanding rapidly (CIRED et al,<br />
1997; Nakicenovic et al, 1997; Grübler, 1998c).<br />
3.6.5. Ozone Precursors<br />
<strong>IPCC</strong> Working Group I (WGI) SAR (Houghton et al, 1996)<br />
confirmed the importance of tropospheric ozone as a<br />
greenhouse gas. Ozone is produced in the troposphere in a<br />
complex chain of reactions that involve the ozone precursors<br />
nitrogen oxides (NO^,), non-CH^ hydrocarbons or volatile<br />
organic compounds (NMVOCs), and CO. Therefore, it is<br />
important to explore possible future developments of emissions<br />
of these substances to analyze the evolution of tropospheric<br />
ozone levels.<br />
3.6.5.1. Nitrogen Oxides<br />
N0^ are released through fossil fuel combustion (24 MtN per<br />
year around 1990), natural and anthropogenic soil release (12<br />
MtN per year), biomass burning (8 MtN per year), lightning (5<br />
MtN per year), NH3 oxidation (3 MtN per year), aircraft (0.4<br />
MtN/year), and transport from the stratosphere (0.1 MtN per<br />
year). These figures are mean estimates within a range; for fossil<br />
fuel combustion, aircraft emissions, and stratospheric input the<br />
ranges may be as narrow as 30%, but for natural sources the<br />
ranges may be up to a factor of 2 (Prather et ai, 1995). The<br />
uncertainties in the estimates are illustrated by comparison of<br />
the detailed emissions inventory of Olivier et al. (1996) with the<br />
1994 <strong>IPCC</strong> estimates - while global total emissions estimates by<br />
source are very similar, at the regional level emissions estimates<br />
show pronounced differences, particularly in Asia.<br />
Fossil fuel combustion in the electric power and transport<br />
sectors is the largest source. <strong>Emissions</strong> from fossil fuel use in<br />
North America and Europe have barely increased since 1979<br />
because fossil fuel consumption leveled off and air quality<br />
abatement was enacted, but in Asia emissions are believed to<br />
increase by 4% annually (Prather et ai, 1995). As a result of the<br />
first NOjj Protocol in Europe, N0^^ emissions in Europe had<br />
decreased from 1987 levels by 13% in 1994, but the European<br />
Union is unlikely to meet its target of the 5* European Action<br />
Plan of a 30% reduction (EEA, 1999). An important reason is<br />
that it is difficult to abate N0^ emissions in the growing<br />
transport sector. Perhaps critically, there are significant<br />
differences between the characteristics of abatement of SOj and<br />
NOj^ emissions. While both substances have regional<br />
acidification effects, a priority for SO2 abatement is induced by<br />
its important local health effects. Also, whereas SO^ emissions<br />
relate closely to the type of fuel, NO^^ emissions are more<br />
dependent on the combustion technology and condifions.<br />
Few scenarios for N0^, emissions exist beyond the studies for<br />
Europe, North America, and Japan (IS92 scenarios are a notable<br />
exception). New scenarios, such as those by Bouwman and van<br />
Vuuren (1999) and Collins et al. (1999) often still use IS92a as<br />
a "loose" baseline, with new abatement policies added as they<br />
were introduced in the OECD countries after 1992, according to<br />
current reduction plans (CRP). Collins et al. (1999) also explore<br />
a maximum feasible reduction scenaiio, in which European N0^,<br />
emissions decrease by 60% by 2015 and North American<br />
emissions by 5%. In the related CRP scenaiio of Bouwman and<br />
van Vuuren (1999), N0^, emissions in the developing countries<br />
are assumed to decrease also (by more than 10%) by 2015.<br />
These studies, however, should be used with care as the authors<br />
developed their somewhat arbitrary scenarios primarily for<br />
atmospheric chemistry analysis; they are not based on an indepth<br />
analysis of the characteristics of the emissions sources and<br />
potential policies in the various regions outside the OECD.<br />
3.6.5.2. Carbon Monoxide and Non-Methane Hydrocarbons<br />
Prather et al. (1995) estimates the total global emissions of CO<br />
at 1800 to 2700 MtC per year in the decade before 1994. The<br />
most important of the approximately 1000 TgC anthropogenic<br />
sources are technological (300 to 550 MtC per year) and<br />
biomass burning (300 to 700 MtC per year). Technological<br />
sources dominate in the northern hemisphere, and include<br />
transport, combustion, industrial processes, and refuse<br />
incineration. Biomass burning dominates in the southern<br />
hemisphere, and includes burning of agricultural waste,<br />
savanna burning, and deforestation. The detailed,<br />
geographically explicit EDGAR database (Olivier et al., 1996)<br />
has similar emissions estimates for CO. Other sources are<br />
biogenics (60 to 160 MtC per year), oceans (20 to 200 MtC per<br />
year), and oxidation of CH^ (400 to 1000 MtC per year) and of<br />
NMVOCs (200 to 600 MtC per year). To a large extent, this<br />
oxidation nray be considered anthropogenic in origin because<br />
many emissions sources of CH4 and NMVOCs are of an<br />
anthropogenic nature.<br />
Global emissions estimates of NMVOCs are also very<br />
uncertain. Prather et al. (1995) indicate a global total for<br />
anthropogenic NMVOCs of about 140 MtC per year, from road<br />
transport (25%), solvent use (14%), fuel production and<br />
distribution (13%), fuel consumption (34%), and the rest from<br />
uncontrolled burning and other sources. The EDGAR<br />
inventory by Olivier et al. (1996) suggests that global<br />
emissions may be higher (178 MtC per year) because of higher<br />
estimates of emissions from energy production and use. As<br />
with CO, emissions in the northern hemisphere are dominated<br />
by transport and industry, while in the southern hemisphere<br />
biomass and biofue! burning is often the dominant source. In<br />
Europe, emissions of NMVOCs are controlled under the 5*<br />
Environmental Action Programme of the European Union and