The weathering of chlorite in hydrothermally-altered basalt was studied with XRD, TEM and electron microprobe to determine the type and orientation of secondary minerals. Optical examination indicated chlorite assemblages to have altered in two distinct microsites: one microsite near micro-fissures traversing the regolith units, and the other away from the continuous passages. In this paper, weathering mechanisms and products of chlorite present in microsites distant from the micro-fissures are reported. In all the regolith units the original chlorite grain remained intact and was pseudomorphed by secondary products. In the saprock, chlorite altered to corrensite with possible random interstratifications of chlorite and corrensite and corrensite and vermiculite. In the saprolite, corrensite altered to vermiculite. Parallelism of two axes of the products with the host indicated topotactic alteration. In the fine saprolite, vermiculite was found to alter to kaolinite via a randomly interstratified kaolinite-vermiculite stage with a high proportion of kaolinite. Goethite crystallized in between packets of kaolinite, vermiculite and kaolinite-vermiculite. Though the disruption of the crystal structure of vermiculite is necessary in its alteration to kaolinite, the reaction was such as to maintain parallelism of the c axis. The alteration of chlorite to vermiculite was characterized by the loss of Mg and Fe and minor Al, all ions considered to be lost from the brucite-like sheet of chlorite. The Fe released during the alteration of vermiculite to kaolinite is likely to have migrated to micropores to form goethite. The presence of interstratifications of the end-members of layer silicates involved in the reaction sequence suggests that interstratifications are common during layer silicate weathering in environments where space is limited and consequently solution and ionic transport passages are restrictive.
Economically significant and geologically complex veined Cu-Co-Au mineralization was recently discovered at Carlow Castle in the Pilbara region of northwestern Western Australia. The inferred resource estimate for Carlow Castle as of March 2019 is 7.7 million tonnes (Mt) at 1.06 g/t Au, 0.51% Cu, and 0.08% Co, making it one of Australia’s most significant known Cu-Co-Au deposits. Here we provide the first account and scientific analysis of Carlow Castle. This analysis suggests that it is a hydrothermal Cu-Co-Au deposit, with mineralization hosted in sulfide-rich quartz-carbonate veins. The ore is hosted in veins that occur within a pervasively chloritized shear zone through the regionally significant Regal thrust. At Carlow Castle the shear zone associated with this thrust occurs within the Ruth Well Formation, an Archean mafic volcano-sedimentary sequence. Within the mineralized veins the dominant ore minerals are pyrite (FeS2), chalcopyrite (CuFeS2), chalcocite (Cu2S), cobaltite (CoAsS), and electrum (Au,Ag). The genesis of the Carlow Castle deposit is still under investigation; however, the origin of the Cu-Co-Au mineralization is most likely related to the migration of metalliferous fluids along the Regal thrust. Based on Carlow Castle’s stratigraphic position within the Pilbara craton and the craton’s relative stability since the Archean, an Archean age of mineralization is most likely. The distinct Cu-Co-Au enrichment at Carlow Castle makes it unique among Archean ore deposits generally, as the majority of Cu-Co deposits are of maximum Proterozoic age. Therefore, understanding the genesis of the Carlow Castle deposit has important implications for understanding the unique processes through which Cu-Co-Au mineralization outside of basin-hosted ore deposits may be formed, particularly in Archean terranes.
Globally, significant examples of hydrothermal Cu-Co mineralization are rare within Archean greenstone belts, especially relative to the endowment of these terranes with other world-class hydrothermal ore deposits, particularly Au deposits. Using U-Pb geochronology of hydrothermal apatite, this study provides the first absolute age constraints on the timing of mineralization for the Carlow Castle Cu-Co-Au deposit. Carlow Castle is a complex, shear zone-hosted, veined Cu-Co-Au mineral system situated within the Paleo-Mesoarchean Roebourne greenstone belt of the Pilbara craton of northwestern Western Australia. Although U-Pb geochronology of this deposit is challenging due to low levels of radiogenic Pb in synmineralization apatite, mineralization is best estimated at 2957 ± 67 Ma (n = 61). Additionally, analysis of alteration phases associated with Carlow Castle mineralization suggests that it is dominated by a propylitic assemblage that is characteristic of alkaline fluid chemistry and peak temperatures >300°C. Within proximal portions of the northwest Pilbara craton, the period of Carlow Castle’s formation constrained here is associated with significant base-metal volcanogenic massive sulfide mineralization and magmatic activity related to back-arc rifting. This rifting and associated magmatic activity are the most likely source of Carlow Castle’s unique Cu-Co-Au mineralization. Carlow Castle’s Meso-archean mineralization age makes it among the oldest discovered Cu-Co-Au deposits globally, and unique in the broader context of hydrothermal Cu-Co-Au deposits. Globally, hydrothermal Cu-Co mineralization occurs almost exclusively as Proterozoic and Phanerozoic stratiform sediment-hosted Cu-Co deposits due to the necessity of meteorically derived oxidized ore fluids in their formation. This research therefore has implications for exploration for atypical Cu-Co deposits and Cu-Co metallogenesis through recognition of comparably uncommon magmatic-hydrothermal Cu-Co-Au ore-forming processes and, consequently, the potential for analogous Cu-Co-Au mineralization in other Archean greenstone belts.
Deposition of Al-Fe-Si-rich clay is pivotal to pavement construction by eucalypts and leads to profound chemical and physical changes in relevant soil profiles. Microbial associates of roots are likely to be involved in clay genesis, with parent eucalypts supplying the required key mineral elements and carbon sources. Acquisition of the Al and Fe incorporated into clay derives principally from hydraulic uplift from ground water via deeply penetrating tap roots.
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