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Emissions Scenarios - IPCC

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Summary Discussions and Recommendations<br />

MtN by 2100 in SRES compared to 5.4 to 10.8 MtN in the IS92<br />

scenarios. (Note that natm-al sources are excluded in this<br />

comparison.)<br />

6.3.2.3. Halocarbons and Halogenated Compounds<br />

The emissions of halocarbons (chlorofluorocarbons (CFCs),<br />

hydrochlorofluorocarbons (HCFCs), halons, methylbromide,<br />

and hydrofluorocarbons (HFCs)) and other halogenated<br />

compounds (polyfluorocaitons (PFCs) and sulfur hexafluoride<br />

(SFg)) across the SRES scenarios are described in detail on a<br />

substance-by-substance basis in Chapter 5 and Fenhaim (2000).<br />

However, none of the six SRES models has its own projections<br />

for emissions of ozone depleting substances (ODSs), their<br />

detailed driving forces, and their substitutes. Hence, a different<br />

approach for scenario generation was adopted.<br />

First, for ODSs, an external scenario, the Montreal Protocol<br />

scenario (A3, maximum allowed production) from<br />

WMO/UNEP (1998) is used as direct input to SRES. In this<br />

scenario corresponding emissions decline to zero by 2100 as a<br />

result of international environmental agreements, a<br />

development not yet anticipated in some of the IS92 scenarios<br />

(Pepper et ai, 1992). For the other gas species, most notably<br />

for CFC and HCFC substitutes, a simple methodology of<br />

developing different emissions trajectories consistent with the<br />

aggregate SRES scenario driving force assumptions<br />

(population, GDP, etc.) was developed. <strong>Scenarios</strong> are equally<br />

further differentiated as to assumed future technological<br />

change and control rates for these gases, varied across the<br />

scenarios consistently within the interpretation of the SRES<br />

storylines presented in Chapter 4. The literature, as well as the<br />

scenario methodology and data, are documented in more detail<br />

in Fenhann (2000) and are summarized in Chapter 5.<br />

Second, different assumptions about CFC applications as well<br />

as substitute candidates were developed. These were initially<br />

based on Kroeze and Reijnders (1992) and information given<br />

in Midgley and McCulloch (1999), but updated with the most<br />

recent information from the Joint <strong>IPCC</strong>/TEAP Expert Meeting<br />

on Options for the Limitation of <strong>Emissions</strong> of HFCs and PFCs<br />

(WMO/UNEP, 1999) as described below. An important<br />

assumption, on the basis of the latest information from the<br />

industry, is that relatively few Montreal gases will be replaced<br />

fully by HFCs. Current indications are that substitution rates of<br />

CFCs by HFCs will be less than 50% (McCulloch and<br />

Midgley, 1998). In Fenhann (2000) a further technological<br />

development is assumed that would result in about 25% of the<br />

CFCs ultimately being substituted by HFCs (see Table 5-9 in<br />

Chapter 5). This low percentage not only reflects the<br />

introduction of non-HFC substitutes, but also the notion that<br />

smaller amounts of halocarbons will be used in many<br />

applications when changing to HFCs (efficiency gains with<br />

technological change). A general assumption is that the present<br />

trend, not to substitute with high GWP substances (including<br />

PFCs and SFg), will continue. As a result of this assumption,<br />

the emissions reported here may be underestimates. This<br />

substitution approach is used in all four scenarios, and the<br />

311<br />

technological options adopted are those known at present.<br />

Further substhution away from HFCs is assumed to require a<br />

climate policy and is therefore not considered in SRES<br />

scenarios. Policy measures that may indirectly induce lower<br />

halocai-bon emissions in the scenarios are adopted for reasons<br />

other than climate change. For one scenario (A2) no<br />

reductions were assumed, whereas in the other scenarios<br />

intermediary reduction rates and levels were assumed.<br />

Expressed in HFC-134a equivalents (based on SAR<br />

equivalents), HFCs in the SRES scenarios range between 843<br />

and 2123 kt HFC-134a equivalent by 2100, compared to 1188<br />

to 2375 kt HFC-134a equivalent in IS92. The range of<br />

emissions of HFCs in the SRES scenario is initiaUy generally<br />

lower than in earlier <strong>IPCC</strong> scenarios because of new insights<br />

about the availability of alternatives to HFCs as replacements<br />

for substances controlled by the Montreal Protocol. In two of<br />

the four scenarios in the report, HFC emissions increase<br />

rapidly in the second half of the 2P' century, while in two<br />

others the growth of emissions is significantly slowed down or<br />

reversed in that period.<br />

Aggregating all the different halocarbons (CFCs, HCFCs,<br />

HFCs) as well as halogenated compounds (PFCs and SFg) into<br />

MtC-equivalents (using SAR GWPs) indicates a range between<br />

386 and 1096 MtC-equivalent by 2100 for the SRES scenarios.<br />

This compares (see Table 6-2b) with a range of 746 to 875<br />

MtC-equivalent for IS92 (which, however, does not include<br />

PFCs and SFg). (The comparable SRES range, excluding PFCs<br />

and SFg, is between 299 and 753 MtC-equivalent by 2100.)<br />

The scenarios presented here indicate a wider range of<br />

uncertainty compared to IS92, particularly toward lower<br />

emissions (because of the technological and substitution<br />

reasons discussed above).<br />

The effect on climate of each of the substances aggregated to<br />

MtC-equivalents given in Table 6-2b varies greatly, because of<br />

differences in both atmospheric lifetime and the radiative effect<br />

per molecule of each gas. The net effect on climate of these<br />

substances is best determined by a calculation of their radiative<br />

forcing - which is the amount by which these gases enhance<br />

the anthropogenic greenhouse effect. The net radiative effect of<br />

all halocarbons, PFCs, and SFg from 1990 to 2100, including a<br />

current estimate of the radiative effect of stratospheric ozone<br />

depletion and subsequent recovery, ranges from 6% to 9% of<br />

the total radiative forcing from all GHGs and SO^. Preliminary<br />

calculations indicate that the net radiafive effect of PFCs and<br />

SFg in SRES scenarios will be no greater, relative to total<br />

anthropogenic forcing, by 2100 than it is at present.<br />

6.3.3. Sulfur Dioxide <strong>Emissions</strong><br />

<strong>Emissions</strong> of sulfur portray even more dynamic pattems in<br />

time and space than the COj emissions shown in Figures 6-5<br />

and 6-6. Factors other than climate change (namely regional<br />

and local air quality, and transformations in the structure of the<br />

energy system and end use) intervene to limit future emissions.<br />

Figure 6-10 shows the range of global sulfur emissions for all

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