1.4 The law of radioactive
decay
The rate of decay of a radioactive parent
nuclide to a stable daughter product is proportional to the number of atoms, n, present at any time t (Rutherford and
Soddy, 1902):
dn
!
)) = 8 n [1.1]
dt
where 8 is the constant of proportionality, which is
characteristic of the radionuclide in question and is called the decay constant
(expressed in units of reciprocal time). The decay constant states the
probability that a given atom of the radionuclide will decay within a stated
time. The term dn/dt is the rate of change of the
number of parent atoms, and is negative because this rate decreases with time.
Rearranging equation [1.1], we obtain:
dn
)) = ! 8 n [1.2]
dt
This expression is integrated from t = 0 to t, given that the number of atoms present at time t = 0 is n0.
n / t/
| dn |
|
)) = ! 8 | dt [1.3]
|
n |
/ n0 /t=0
Hence: n
ln ))
= !
8 t [1.4]
n0
which can also be written as:
n
= n0 e!8t [1.5]
A useful way of referring to the rate of decay
of a radionuclide is the ‘half-life’, t1/2,
which is the time required for half of the parent atoms to decay. Substituting n=n0/2
and t = t1/2 into equation [1.5], and taking the natural log of
both sides, we obtain:
ln
2 0.693
t1/2 = )))
= )))) [1.6]
8 8
The number of radiogenic daughter atoms formed,
D*, is equal to the number
of parent atoms consumed:
D* = n0
! n [1.7]
but n0
= n e8t (from equation [1.5]); so substituting for n0 in equation [1.7] yields:
D* = n e8t ! n [1.8]
i.e:
D* = n (e8t ! 1) [1.9]
If the number of daughter atoms at time t = 0 is D0 , then the total
number of daughter atoms after time t
is given as:
D = D0 +
n (e8t ! 1) [1.10]
This equation is the fundamental basis of most geochronological dating tools.
In
the uranium series decay chains, the daughter products of radioactive decay
(other than three Pb isotopes) are themselves
radioactive. Hence the rate of decay of such a daughter product is given by the
difference between its production rate from the parent and its own decay rate:
dn2/dt =
n1 81 !
n2 82 [1.11]
where n1
and 81 are the abundance and decay
constant of the parent, and n2
and 82 correspond to the daughter.
But
equation [1.5] can be substituted for n1
in equation [1.11] to yield:
dn2/dt =
n1,initial e!81 t 81 !
n2 82 [1.12]
This equation is integrated for a chosen set of
initial conditions, the simplest of which sets n2=0 at t=0.
Then:
81
n2 82
= )))))
n1,initial (e!81 t ! e!82 t) [1.13]
82 ! 81
This type of solution was first demonstrated by
Bateman (1910) and is named after him. Recently, Catchen
(1984) examined more general initial conditions for these equations, leading to
more complex solutions.
1.4.1 Uniformitarianism
When using radioactive decay to measure the
ages of rocks we must apply the classic principle of uniformitarianism
(Hutton, 1788), by assuming that the decay constant of the parent radionuclide
has not changed during the history of the Earth. It is therefore important to
outline some evidence that this assumption is justified.
The
decay constant of a radionuclide depends on nuclear constants, such as a (= elementary charge2/Plank’s
constant/velocity of light). Shlyakhter (1976) argued
that the neutron capture cross-section of a nuclide is very sensitively
dependent on nuclear constants. Because neutron absorbers (such as 143Nd
and 145Nd) in the 1.8 Byr-old Oklo natural reactor give rise to the expected abundance
increases in the product isotopes (Fig. 1.13) this constrains nuclear constants
to have remained more or less invariant over the last 2 Byr.
The
possibility that physical conditions (e.g. pressure and temperature) could
affect radionuclide decay constants must also be examined. Because radioactive
decay is a property of the nucleus, which is shielded from outside influence by
orbital electrons, it is very unlikely that physical conditions influence " or $ decay, but electron capture decay
could be affected. Hensley et al.
(1973) demonstrated that the electron capture decay of 7Be to 7Li
is increased by 0.59% when BeO is subjected to 270 " 10 kbars
pressure in a diamond anvil. This raises the question of whether the electron
capture decay of 40K to 40Ar could be pressure dependant,
affecting K)Ar dates. In fact this is very unlikely, because
at high pressure-temperature conditions at depth in the Earth, K)Ar
systems will be chemically open and unable to yield dates at all, while at crustal depths the pressure dependence of 8 will be negligible compared with
experimental errors.
There
are a few ways in which the invariance of decay constants has been
experimentally verified. Uranium series dates have been calibrated against
coral growth bands back to one thousand years (section 12.4.2), the radiocarbon
method has been calibrated against tree rings (dendrochronology)
back to 10 kyr (section 14.1.4), and K-Ar ages have been calibrated against sea floor spreading
rates over periods of several Myr (section 10.4). In
addition, age agreements between systems with very different
decay constants also provides supporting evidence.
There
have been many attempts to test the consistency of different decay constants by
comparing ages for geologically ‘well behaved’ systems using different dating
methods (e.g. Begemann et al., 2001). As well as
verifying the uniformitarian assumption, such
geological decay constant comparisons allow the values for poorly known decay
schemes to be optimised by comparison with better-known decay schemes. At
present, the uranium decay constants are the most well
established, and therefore the basis for most comparisons. However, a promising
new calibration is the ‘astronomical timescale’, based on the tuning of glacial
cycles to the Earth’s orbital motions (section 10.4).
The best approach to the improvement
of decay constants is new and better measurement. Where this is not possible, a
useful alternative is acceptance by the geological community of a ‘recommended
value’. The most successful application of this procedure was the IUGS Subcommission on Geochronology (Steiger
and Jager, 1977). The recommendations served as a
useful standard for 20 years but are now in need of revision. Therefore, Table
1.1 presents these values where applicable, together with a compilation of the best
decay constant determinations obtained since that time, by various methods. Full
references and further details are given in the appropriate chapters.
Table 1.1 Summary of decay constants and half
lives of long-lived nuclides
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
Nuclide S & J 1977 ‘Best
value’ Half life Reference
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
40K (40Ar) 5.81
E-11 11.93
Byr Beckinsale and
Gale (1969)
40K (40Ca) 4.962 E-10 1.397 Byr
40K (total) 5.543
E-10 1.25
Byr
87Sr 1.42 E-11 1.402 E-11 49.44 Byr Minster
et al. (1982)
147Sm 6.54 E-12 106.0
Byr Lugmair and Marti (1978)
176Lu 1.867 E-11 37.1
Byr Scherer
et al. (2001)
186Re 1.666 E-11 41.6
Byr Smoliar et al. (1996)
190Pt 1.477 E-12 469.3
Byr Brandon
et al. (1999)
230Th 9.1577 E-6 75.69 kyr Cheng et al. (2000)
232Th 4.9475 E-11 14.01 Byr Jaffey et al. (1971)
231Pa 2.116 E-5 32.76 kyr Robert
et al. (1969)
234U 2.826 E-6 245.25 kyr Cheng
et al. (2000)
235U 9.8485 E-10 unchanged 703.8
Myr Jaffey et al. (1971)
238U 1.55125
E-10 unchanged 4468.0 Myr Jaffey
et al. (1971)
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
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