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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

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