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depend on thermal activation, the probability
of ‘climbing’ a barrier of energy E being propor-
tional to exp(E/kT) at temperature T. The effect
of stress may be to reduce E for displacements in
favoured directions and increase it for opposite
movements, or merely give greater opportunity
for favoured displacements, imparting a statisti-
cal bias to the movements that occur. Of course,
macroscopic crystal deformation involves seq-
uences of atomic movements with different
barrier energies; the highest barriers are rate-
controlling and determine the activation energy
for the whole process. In fine grained mater-
ials, grain boundary effects become important.
Although superficially similar to frictional slid-
ing between grains, they involve individual
atomic displacements that accommodate boun-
dary fitting. Like diffusion or dislocation creep,
they are relaxation phenomena.
Pressure, P, makes all atomic movements
more difficult and so increases barrier energies.
This is often represented by writing E ¼E þPV
,
with the constant V
referred to as activation
volume. However, in a geophysical context it
is more convenient to relate E to melting point,
T
M
, by writing
E ¼ gkT
M
; (10:26)
where k is Boltzmann’s constant and g is a
dimensionless factor t hat is found to average
about 27 for common minerals (Poirier, 2000).
Equation (10.26) incorporates the pressure-
dependence of E because melting depends on
the same sort of atomic displacements as are
responsible for solid creep. As discussed in
Section 17.4, melting can be regarded as a free
proliferation of crystal dislocations, a liquid
being a crystal saturated with dislocations. The
increase in T
M
with pressure mirrors the increase
in E, so that the variation of inelastic deforma-
tion with depth in the Earth is modelled with
a theory of the variation of T
M
with P.
Progressive deformation of the mantle occurs
by steady state creep and can be represented by
a general equation (Weertman and Weertman,
1992)
d"=dt
_
" ¼ Bð=Þ
n
expðgT
M
=TÞ; (10:27)
where B is a constant. This equation incorporates
both temperature and pressure dependences,
by virtue of the pressure effect on T
M
, and allows
for a variety of mechanisms by the arbitrary
index, n. The familiar case of Newtonian visco-
sity requires n ¼1, with strain rate,
_
", propor-
tional to stress, . Crystal deformation by
diffusion of point defects (Nabarro–Herring
creep) is of this form. Dislocation-dominated
creep occurs in different regimes with different
values of n, between 1 and 6; n ¼3 is commonly
favoured.
Regarding a liquid as a fully dislocated solid,
we can consider fluid flow to be a special case of
dislocation-mediated steady-state creep, with no
essential distinction between solid and liquid,
except for the concentration of dislocations. In
this case, with n ¼1 in Eq. (10.27), viscosity, ,is
an unambiguous material property,
¼ =
": (10:28)
Its SI unit is the pascal-second (Pa s). While vali-
dity of the n ¼1 assumption is not as clear in the
Earth, we nevertheless refer to viscosity for all
layers below about 70 km, where the tempera-
ture is high enough for steady state creep to
occur. The uppermost 70 km (the lithosphere) is
too cool to be treated in this way and, depending
on the phenomenon to be analysed, may be
regarded as elastic (or perhaps subject to tran-
sient creep) or, for the uppermost layer, with
deformation analysed by a rock mechanics
approach, as in Chapter 11.
The homologous temperature, T/T
M
, appears
in the exponential term of the general creep law
(a) (b)
FIGURE 10.5 Displacements that produce (a) a screw
dislocation and (b) an edge dislocation. The cylinders
have been drawn as hollow to avoid difficulty with the
discontinuity in displacement on the dislocation axes,
which are cylinder axes.
146 ELASTIC AND INELASTIC PROPERTIES