E. Vindel et al., P-V-T-X-FO2 EVOLUTION FROM WOLFRAMITE TO SULFIDE DEPOSITIONAL STAGES IN INTRAGRANITIC W-VEINS - AN EXAMPLE FROM THE SPANISH CENTRAL SYSTEM, European journal of mineralogy, 7(3), 1995, pp. 675-688
The relative P-T-X conditions of the deposition of wolframite and sulp
hides in quartz veins has been investigated using representative W-pol
ymetallic sulphide veins hosted by peraluminous granites in the centra
l domain of the Spanish Central System. Ore-bearing quartz veins fall
into two groups: W-veins (wolframite-bearing quartz veins with minor a
mounts of sulphides) and sulphide (S) dominated veins (wolframite free
). The two vein types (S and W) have similar orientation, silicate and
sulphide mineralogy. A multidisciplinary approach based on a detailed
fluid-inclusion analysis in relation with a paragenetic reconstructio
n of vein fillings suggests a similar genesis and fluid history, as fo
llows: (i) an early fluid stage, lacking in S-veins, characterized by
CO2-H2O-NaCl rich vapours is at the origin of a strong K-mica alterati
on of the granite wall-rock, and of vein filling by milky quartz (QI)
- phengite I - (wolframite), at around 130 +/- 20 MPa and 525 +/- 25-d
egrees-C; (ii) a second stage characterized by H2O-CO2-CH4-NaCl fluids
with a low volatile-phase density, at the origin of the deposition of
: a) saccharoidal quartz (QII) (+ phengite II and minor amounts of sc
heelite in W-veins), and then, b) a chlorite-sulphide (pyrrhotite, sph
alerite and galena) assemblage. A progressive decrease of the CO2 cont
ent in fluids is recorded, CH4 being the major volatile species in the
latest inclusions spatially associated with sulphides. Pressure is ar
ound 130 +/- 30 MPa, and temperature decreases from 380-degrees to 330
-degrees-C throughout the course of the fluid trapping. iii) later flu
id inputs in the veins are shown by two types of secondary aqueous flu
id inclusions in healed microfissures, which display moderate Th (160-
degrees-220-degrees-C) and salinites. The two main stages (wolframite,
then sulphides) are characterized by a nearly isobaric cooling and di
lution of volatile rich fluids. The X-fO2 evolution indicates that flu
id chemistry was probably controlled during the first stage by graphit
e-fluid equilibrium, implying a fluid source external to the granite (
surrounding metamorphic series). The sulphide stage, which is ubiquito
us in most W deposits, appears clearly in this example as the latest s
tage of a primary hydrothermal cycle involving volatile bearing fluids
, and is not disconnected from the W stages.