Atacamite in the oxide zone of copper deposits in northern Chile: involvement of deep formation waters?
Author
dc.contributor.author
Cameron, Elion M.
Author
dc.contributor.author
Leybourne, Matthew I.
es_CL
Author
dc.contributor.author
Palacios Monasterio, Carlos
es_CL
Admission date
dc.date.accessioned
2013-12-26T17:07:44Z
Available date
dc.date.available
2013-12-26T17:07:44Z
Publication date
dc.date.issued
2007
Cita de ítem
dc.identifier.citation
Miner Deposita (2007) 42:205–218
en_US
Identifier
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DOI 10.1007/s00126-006-0108-0
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/125854
Abstract
dc.description.abstract
Atacamite, a copper hydroxychloride, is an
important constituent of supergene oxide zones of copper
deposits in northern Chile, whereas in similar deposits
elsewhere, it is rare. In Chile, it has generally been assumed
to be a primary constituent of the supergene zones. There
are two difficulties with this supposition. The first is that
atacamite requires saline water for its formation, whereas
supergene oxidation was caused by percolating, oxygenated
meteoric water, mainly rainwater. The second is that
atacamite dissolves rapidly or undergoes phase change
when exposed to fresh water. Supergene enrichment of
copper deposits in northern Chile extended over a long
period, 44 to 9 Ma, being terminated by the onset of
hyperaridity. During this period, there was at least intermittent
rainfall, exposing previously formed atacamite to
dissolution or phase change. Furthermore, atacamite-bearing
oxide zones in several deposits are directly overlain by
thick Miocene alluvial gravels; the stream waters that
transported these gravels would have permeated the oxide
zones. In some deposits, atacamite-bearing assemblages
occur both in the oxide zones and in contiguous gravels.
We suggest that atacamite-bearing oxide assemblages are
more likely to have been a replacement of preexisting oxide
phases after the onset of hyperaridity at about 9 Ma. A
hyperarid climate made possible evaporation and concentration
of chloride in meteoric waters. In this paper, we
discuss another source of saline waters to modify oxide
zones. Dewatering of the Domeyko Basin expelled brines
along faults, some of which had earlier guided the location
of porphyry deposits. At the Spence porphyry copper
deposit, saline waters, which δD vs δ18O isotope analyses
identify as basinal brines, are presently rising through the
deposit, then flowing away along the base of the covering
gravels. Compositions of these waters lie within the
stability fields of atacamite and brochantite, the two
minerals that comprise the oxide zone. Evidence is
presented for other porphyry deposits, Radomiro Tomic
and Gaby Sur, that basinal brines may have been involved
in the late formation of atacamite.