High-precision stepped-heating experiments were:performed to better charact
erize helium diffusion from apatite using Durango fluorapatite as a model s
ystem. At temperatures below 265 degrees C, helium diffusion from this apat
ite is a simple, thermally activated process that is independent of the cum
ulative fraction of helium released and also of the heating schedule used.
Across a factor of similar to 4 in grain size, helium diffusivity scales wi
th the inverse square of grain radius, implying that the physical grain is
the diffusion domain 1. Measurements on crystallographically: oriented thic
k sections indicate that helium diffusivity in Durango apatite is nearly is
otropic. The,best estimate of the activation energy for He diffusion from t
his apatite is E-a = 33 +/- 0.5 kcal/mol, with log(D-0) = 1.5 +/- 0.6 cm(2)
/s. The implied He closure temperature for a grain of 100 mu m radius is 68
degrees C assuming a 10 degrees C/Myr cooling rate; this figure varies by,
+/-5 degrees C for grains ranging from 50 to 150 mu m radius. When this ap
atite is heated to temperatures from 265 to 400 degrees C, a progressive an
d irreversible change in He diffusion:behavior occurs: Both the activation:
energy and frequency factor are reduced. This transition in behavior coinci
des closely with progressive annealing of radiation damage in Durango apati
te, suggesting that defects and defect annealing play a role in the diffusi
vity of helium through apatite.