
211 The radiative forcing due to an increase in carbon dioxide
The final stage in the calculation of the radiative forcing is to integrate the spectral
results over frequency, i.e. to calculate the areas under the curves in Figure 8.6(b).
3
(See
Problem 8.9.) The fact that these areas depend only weakly on β shows that the approximate
logarithmic dependence carries over to the radiative forcing F, which therefore takes the
form
F =−
∞
0
F
↑
ν
dν ≈ A ln β, (8.30)
where A is a constant, in agreement with the form of equation (8.24). Note that the
logarithmic dependence does not depend on the detailed structure of the spectral lines, but
just on the fact that the tropospheric transmittance varies rapidly in frequency between 0 and
1 on each flank of the absorption band, so that the most significant values of the transmittance
change (almost proportional to ln β) are attained in a narrow range of frequencies there.
The integral is dominated by contributions from frequencies in these flank regions.
For comparison with Section 8.2, it is convenient to put U = ln ρ
0
,whereρ
0
= ρ
a
(0)
is the CO
2
density at the ground. The change from ρ
0
to βρ
0
then corresponds to the finite
change U = ln β,soequation (8.30) gives F ≈ A U.Thisimpliesthatequation (8.7)
holds without the ‘small perturbation’ assumption, given ∂Q/∂U = A.
The CO
2
case should be contrasted with that of absorbers such as the chlorofluorocarbons,
which are optically thin at all frequencies, so that T
ν
is always close to 1 (i.e. it is always
close to the right-hand end of the range shown in Figure 8.4), and D
max
is never attained
at any ν. In this case we can show (e.g. by putting T
ν
= 1 − A
ν
,whereA
ν
1) that
D(T
ν
) ∼ (β − 1)(1 − T
ν
). Therefore for such absorbers the radiative forcing is linear, not
logarithmic, in β: this is confirmed by detailed calculations.
Of course, our simple slab model is an extremely crude representation of the real
troposphere. However, it can be extended to a multi-level model in which the temperature
follows a specified lapse rate; the argument that we have used is applied at each level
within the troposphere, and then a vertical integral performed. Approximate logarithmic
dependence of the SOLR at each frequency is found, and essentially the same results follow.
Further reading
A good introduction to the physics of climate change is given by Hartmann (1994). The
advanced but readable book by Pierrehumbert (2010) covers the material of this chapter
in more detail, and goes much further – including, for example, the physics of climate
change in the Earth’s distant past and on other planets. The Fourth Assessment Report of
the Intergovernmental Panel on Climate Change, Working Group I (Solomon et al. (2007)),
gives a wealth of up-to-date information on climate change and the physical processes
contributing to it. Houghton (2009) provides an authoritative overview of the current
3
This is almost identical to integrating the unsmoothed functions, since the smoothing just reorders them with
respect to frequency. The Planck function is not reordered; however, it only varies slowly with frequency. Note
also that other CO
2
absorption bands are present, as shown by Figure 3.14, but these are less important because
B
ν
is much smaller for the frequencies and temperatures involved.