D. Selby et al., Hydrothermal alteration and fluid chemistry of the Endako porphyry molybdenum deposit, British Columbia, ECON GEOL B, 95(1), 2000, pp. 183-201
Citations number
88
Categorie Soggetti
Earth Sciences
Journal title
ECONOMIC GEOLOGY AND THE BULLETIN OF THE SOCIETY OF ECONOMIC GEOLOGISTS
Hydrothermal alteration and fluid chemistry data of the early Cretaceous En
dako porphyry molybdenum deposit, British Columbia, provide new information
on the hydrothermal fluids associated with low-fluorine molybdenite minera
lization. Molybdenite mineralization and hydrothermal alteration occur as e
arly quartz +/- molydenite stockwork veins with K feldspar-bearing salvages
and paragenetically later quartz-molybdenite ribbon veins with sericite-be
aring selvages. Late hydrothermal alteration is associated with the develop
ment of kaolinite and postore (Tertiary age) calcite veins.
Fluid inclusions in early-formed quartz +/- molybdenite stockwork veins wit
h K feldspar-bearing alteration assemblages are dominated by moderate salin
ity (5 to 15 wt % NaCl equiv), liquid-rich (type 1) and rare high-salinity
(30 to 45 wt % NaCl equiv), halite-bearing (type 3) fluid inclusions. Type
1 and type 3 fluid inclusions in early veins homogenize between 390 degrees
and 430 degrees C and 375 degrees and 420 degrees C, respectively. Seconda
ry fluid inclusions (type 2) of low salinity (1 to 5 wt % NaCl equiv) in th
ese early veins are minor, and homogenize between 130 degrees and 285 degre
es C. Fluid inclusions in quartz-molybdenite ribbon veins with sericite-bea
ring alteration assemblages are dominated by moderate-salinity, liquid-rich
(type 1) inclusions, with minor type 2 fluid inclusions. Type 1 fluid incl
usions of ribbon veins homogenize between 360 degrees and 400 degrees C. Fl
uid inclusions in postore cal cite veins are of only type 2 fluid inclusion
s, which homogenize at 209 degrees C. Hydrothermal fluids recorded by type
I and type 3 fluid inclusions in early veins were trapped under lithostatic
to hydrostatic conditions between 0.3 and less than or equal to 2.0 kbar,
and 360 degrees and 560 degrees C. Postore fluids recorded by type 2 fluid
inclusions were trapped under conditions less than or equal to 0.5 kbar, an
d between 190 degrees and 300 degrees C.
Quartz stockwork and ribbon Veins possess delta(18)O values of 8.4 +/- 0.2
(n = 9) and 8.4 +/- 0.6 (n = 13), respectively. Hydrothermal K feldspar and
biotite from K feldspar alteration assemblages possess delta(18)O values o
f 6.8 +/- 0.4 (n = 7) and 3.5 +/- 0.8 (n = 8), respectively. Oxygen isotope
geothermometry of quartz-biotite and quartz-K feldspar pairs from K feldsp
ar alteration assemblages yield temperatures between 200 degrees and 490 de
grees C, which is similar to the trapping temperatures of hydrothermal flui
ds determined from fluid inclusion studies associated with molybdenite mine
ralization, the development of kaolinite, and calcite veins. The oxygen iso
tope temperatures of the quartz-biotite and quartz-K feldspar pairs suggest
that K feldspar and biotite either record the approximate O-18 composition
of hydrothermal fluids associated with K feldspar alteration or have under
gone O-18 exchange with late-stage hydrothermal fluids. Hydrogen isotope co
mposition of quartz stockwork and ribbon veins fluid inclusion waters range
between -105 and -113 per mil.
Solute chemistry studies of fluid inclusion waters indicate that ore formin
g fluids from Endako have low Br/Cl and Br/Na ratios, and high I/Cl and I/B
r ratios in comparison to Porgera (epithermal), Babine Lake (porphyry Cu),
and St. Austell, Capitan Pluton (vein) deposits associated with magmatic pr
ocesses. Na/K ratios of fluid inclusion waters yield temperatures (308 degr
ees to 429 degrees C) similar to those determined from type 1 and type 3 fl
uid inclusions and stable isotope thermometry.
Results from fluid inclusion and solute chemistry studies indicate the invo
lvement of hydrothermal fluids exsolved from a crystallizing melt in the fo
rmation of the Endako molybdenum deposit. However, oxygen and hydrogen isot
ope values deviate from the generally accepted magmatic compositions, which
suggests the early involvement of meteoric water in the ore-forming fluids
and ore genesis.