The
Coastal Cordillera metallogenic province of northern Chile
comprises several styles of mineralization, including stratabound
Cu–(Ag), iron oxide–copper–gold (IOCG), iron
oxide–apatite (IOA), and porphyry Cu deposits. Stratabound
Cu–(Ag) or “Manto-type” deposits from the Coastal
Cordillera of northern Chile formed during two main periods, i.e.,
the Late Jurassic and Early Cretaceous. These deposits are hosted
in volcanic and volcano sedimentary rocks, and some of them are characterized
by the presence of solid hydrocarbons (bitumen), which are closely
associated with pyrite and Cu–(Fe) sulfides. Although pyrite
is ubiquitous and in some cases abundant in this deposit type, its
trace element content and mineralogical form of incorporation, i.e.,
nanoscale inclusions or solid solution, remains largely unknown. In
this study, we focus on pyrite from bitumen-bearing stratabound Cu–(Ag)
deposits from northern Chile to assess the formation conditions of
these deposits by using a combination of electron probe microanalysis
(EPMA) and laser ablation inductively coupled plasma mass spectrometry
(LA-ICP-MS). Our results show that pyrite from stratabound Cu–(Ag)
deposits hosts significant concentrations of Cu, As, Mn, Pb, Tl, Co,
Ni, V, and Mo that range from a few parts per million (ppm) to weight
percent (wt %) levels. Among all elements analyzed, Cu, As, Mn, and
Tl are the most abundant, reaching concentrations up to ∼2.8
(Cu), ∼0.25 (As), ∼2.4 (Mn), and ∼0.09 wt % (Tl).
These elements occur dominantly in solid solution, although LA-ICP-MS
depth profiles suggest the presence of micro- to nanosized mineral
inclusions. Pyrite from stratabound Cu–(Ag) deposits is characterized
by distinctively lower Co/Ni (∼0.1 to 10) and Co/Cu ratios
(∼0.0001 to 10) and higher Ag/Co values (∼0.001 to 10)
than pyrite from Cretaceous iron oxide-apatite (IOA) and IOCG deposits
from the Coastal Cordillera metallogenic province. We interpret these
variations as resulting from differences in physicochemical parameters
of the pyrite-forming fluid, i.e., temperature, redox conditions,
and source of metals/sulfur. Based on our data we conclude that pyrite
from the studied stratabound Cu–(Ag) deposits formed at relatively
low temperatures (100 to ∼300 °C), reducing conditions,
and with a strong sedimentary component as reflected in its trace
element geochemistry. Therefore, our data supports the use of the
trace element content of pyrite to fingerprint the formation conditions
of ore mineralization in different deposit types with possible applications
as a vectoring tool within the Coastal Cordillera metallogenic province
and elsewhere.