The high retentivity of monazite for Pb, its high U and Th concentrati
ons, and its emergence in staurolite-zone metapelites suggests its use
as a prograde thermochronometer. However, the monazite-producing reac
tions in pelites are as yet incompletely understood. We have investiga
ted by experiment the suggestion that rhabdophane (LREEPO(4).nH(2)O) s
hould be considered as an important reactant in monazite-producing rea
ctions in pelitic compositions. Results of our combined hydrothermal a
nd 1-bar heating experiments preclude rhabdophane from being the immed
iate precursor to neoformed monazite in lower amphibolite-facies metam
orphic sequences and restrict rhabdophane occurrence to the uppermost
portion of the crust. Dehydration of rhabdophane to form monazite appe
ars to occur in a manner that may be analogous to the dehydration equi
libria of zeolite minerals. Dry, 1-bar heating experiments indicate th
at La-rhabdophane persists (metastably?) to temperatures approaching 5
00 degrees C. XRD and visible-near-infrared spectroscopy examination o
f La-rhabdophane heated isothermally in air at temperatures ranging fr
om 200 degrees to 700 degrees C indicate that structural water is larg
ely retained up to 500 degrees C over heating intervals of up to 24 hr
. Structural modifications involving H2O appear to take place between
300 degrees and 500 degrees C. Partial decomposition of La-rhabdophane
to La-monazite is observed at 600 degrees C while rapid and complete
reaction to La-monazite occurs at 700 degrees C. Experiments conducted
under elevated water pressure (0.5-2 kbar) at temperatures between 20
0 degrees and 600 degrees C have not encountered conditions under whic
h rhabdophane is stable relative to La-monazite+H2O, The low rhabdopha
ne dehydration temperatures relative to the temperatures inferred for
monazite formation in metapelites indicate that rhabdophane does not c
onvert directly to monazite during pelite metamorphism. Rather, the ''
monazite LREE component'' produced by rhabdophane breakdown must be in
corporated in intermediate phases such as allanite and, perhaps more l
ikely, LREE-oxides prior to monazite formation.