The geology, geochemistry and geochronology of the El Abra Mine, Chile, and the adjacent Pajonal-El Abra suite of intrusions
Date
2008
Authors
Valente, Dianne Lee
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Abstract
The El Abra Porphyry Copper Deposit is a major deposit located 1650 km north of
Santiago in the El Loa Province, Northern Chile. It occurs within the Late Eocene-
Oligocene aged, north-south trending, Domeyko Cordillera which hosts a number
of major copper-porphyry deposits including Chuquicamata. The deposit is
spatially associated with the El Abra - Pajonal igneous suite consisting of eleven
calc-alkaline intrusions ranging in composition from alkali feldspar granite to
quartz monzodiorite.
El Abra - Pajonal suite whole-rock and mineral chemistry show that these
intrusions were emplaced between 43.4 - 35.5 Ma as a series of short-lived,
shallow-crustal chambers located at pressures less than 2 kbar. A long-lived, midcrustal
chamber located at pressures between 5 - 11.5 kbar underpinned these
chambers. Crystal fractionation and assimilation were the key magmatic processes
influencing the suites’ evolution within magma chambers at both crustal levels.
Pyroxene fractionation was initially dominant in the mid-crustal chamber, however
after ~41 Ma, decreasing whole-rock Fe, Mg. Dy. Y. Ni concentrations showed that
amphibole fractionation became progressively dominant reflecting increasing
magmatic water concentrations. Magma was tapped periodically from the midcrustal
chamber producing a series of upper-crustal chambers in which plagioclase
and amphibole were the dominant crystallizing phases. Plagioclase fractionation is
recognized by decreasing whole-roek Sr, Ba and A1 concentrations and large
negative Eu anomalies.
At 40.8 Ma, a mixing event occurred between an injected, mantle-derived, mafic
magma with the magma evolving in the mid-crustal chamber. The mafic magma is
interpreted to have provided a source for copper and sulfur in addition to providing
a heat source that promoted partial melting of the surrounding wall rock, composed
of amphibolites and meta-andesites. Magnetite assimilation was one process
causing the oxygen fugacity of the evolving mid-crustal magma to increase through
time. Due to the magmas' high oxygen fugacity, the sulfur species in the melt on
the basis of S concentrations in apatite was S , and therefore at sulfur-saturation, copper remained in the silicate melt. Assimilation of amphibolites and metaandesites
at the mid-crustal level also enhanced the water concentration of the
evolving magma through the break-down of amphibole. As the magma became
water-saturated, a fluid phase formed in the lower chamber and copper dissolved in
the silicate melt partitioned into that phase. Copper then precipitated from the
mineralizing fluid phase when it reached shallow crustal levels.
Differences in the averaged Cu concentrations between shallowly crystallized
plagioclase cores and rims show that as intermediate composition intrusions were
emplaced into shallow levels, minor mineralization events occurred. Zircon
0 / O values up to l%o greater than mantle-derived zircon, rare Cu-rich xenoliths
and the El Abra - Pajonal suite's zircon inheritance record suggest that assimilation
may have contributed additional copper to El Abra - Pajonal suite magmas as they
continued to evolve. However, the main mineralization event is associated with the
emplacement of the El Abra porphyry at 36.9 Ma. because the parental mid-crustal
magma to this intrusion was the most oxidized and hydrous of the suite and hence
the most efficient in extracting Cu from the silicate melt to the fluid phase. The
rapid emplacement of the El Abra porphyry into the upper crust aided precipitation
of copper from the exsolving fluid phase and helped to generate the highest
yielding hydrothermal fluid that is associated with this intrusion.
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