Hydrogen isotope investigations on hydrothermal quartz reveal two H-reservo
irs: (i) trapped fluid inclusions, and (ii) structurally bound water in hom
ogenously distributed small clusters or bubbles. Varying mixing ratios of t
he two reservoirs are sampled by means of mechanical and thermal decrepitat
ion applied to different grain size fractions. A two-component mixing calcu
lation results in an isotopic characterisation of the two H-reservoirs, whi
ch fractionate hydrogen isotopes close to the known MOH-H2O system, with wa
ter being enriched in deuterium. Temperature controls both the internal fra
ctionation as well as the abundance ratio of inclusion water to bonded wate
r. At high temperatures, fractionation is small but bound water becomes mor
e abundant, comprising a significant amount of water from both thermal and
mechanical extraction techniques. Hence, the isotope composition of the ext
racted water does not reflect the original hydrogen isotope composition of
the hydrothermal fluid especially at temperatures higher than 200 degreesC.
Previously reported deltaD data of fluid inclusion, which were used to elu
cidate the origin of the hydrothermal fluid, tend to be too low. (C) 2001 E
lsevier Science B.V. All rights reserved.