ALBERT

Description: Exploration geochemical and mineralogical studies by the U.S. Geological Survey at the Pebble porphyry Cu-Au-Mo deposit were designed to (1) determine whether the concealed deposit can be detected with surface samples, (2) better understand the processes of metal migration from the deposit to the surface, and (3) test existing methods for assessing concealed mineral resources and/or develop new ones. Surface water (ponds, streams, and springs), pond and stream sediment, soils subjected to various leaching techniques, and glacial till samples were collected. The tilted nature of the undisturbed orebody, varying depth of cover, and later glacial processes, strongly influence the geochemical responses and processes active on the various sample media. The multimedia approach aids in identifying possible processes that caused the significant geochemical variations within and among the various media. These processes include the following: In the Pebble West zone, thin cover and local exposure of the orebody have facilitated the oxidation of pyrite and other sulfides, and associated ferrous-ferric iron reactions, resulting in the local natural acidification of ponds observed in the West zone, and in associated metal anomalies in waters, sediments, and soils. In contrast, the East zone is concealed by both glacial deposits and underlying thick cover rocks, which precludes the oxidation of sulfides in the underlying orebody. Low-level geochemical anomalies in circumneutral spring and pond waters from the East zone are discernible only by using high resolution-inductively coupled plasma-mass spectrometry with lower limits of determination two and perhaps three orders of magnitude lower than traditional methods. A variety of partial leaches of soils over the East zone reveal geochemical anomalies in a similar suite of elements that may be related to upwelling waters from depth along graben-bounding faults. The indicator minerals gold, jarosite, and andradite in till reveal a displaced mineralogical anomaly to the west and south of the Pebble orebody, as ore-related minerals were scraped from the orebody and deposited in till downice of the deposit. Geochemical anomalies in pond water and sediment over the displaced till are attributed to the ore-related minerals in till. This orientation study demonstrates the strong control of local geologic and geochemical settings on the effectiveness of different traditional and newer reconnaissance geochemical exploration techniques and thus has important implications for exploration.

Description: Review and analysis of initial lead isotope ratios from Archean volcanic-hosted massive sulfide (VHMS) and lode gold deposits and of neodymium isotopes from igneous rocks from the geologic provinces that host these deposits identifies systematic spatial and temporal patterns, both within and between the provinces. The Abitibi-Wawa subprovince of the Superior province is characterized by highly juvenile lead and neodymium. Most other Archean provinces, however, are characterized by more evolved isotopes, although domains within them can be characterized by juvenile isotope ratios. The analysis indicates that the endowment (measured as the quantity of metal contained in geologic resources per unit surface area) of VHMS and komatiite-associated nickel sulfide deposits is related to the isotopic character and, therefore, the tectonic history of provinces that host these deposits. Provinces with extensive juvenile crust have significantly higher endowment of VHMS deposits, possibly as a consequence of higher heat flow and extension-related faults. Provinces with evolved crust have higher endowment of komatiite-associated nickel sulfide deposits, possibly because such crust provided either a source of sulfur or a stable substrate for komatiite emplacement. In any case, initial radiogenic isotope ratios can be useful in predicting the endowment of Archean terranes for VHMS and komatiite-associated nickel sulfide deposits. Limited data suggest similar relationships may hold in younger terranes. Lead isotope data may provide constraints on supercraton reconstructions in the Archean as lead isotope systematics appear to be highly provincial. Similar isotope systematics between the Superior province and the Eastern Goldfields superterrane may indicate a linkage during the Neoarchean, consistent with the similar geologic and metallogenic histories of these provinces.

Description: The Jbel Tirremi fluorite-barite ± sulfide deposit in northeastern Morocco is hosted in a Jurassic-aged structurally high carbonate platform known as the Jbel Tirremi dome. The host rocks consist of unmetamorphosed, flat-lying early Jurassic dolomitized limestones, locally intruded by Eocene lamprophyre dikes. The orebodies consist mostly of fluorite and barite, and occur as open-space fillings and partial to massive replacement of the enclosing medium- to coarse-grained dolomitized limestones. The ore mineralogy is dominated by fluorite of different colors and habits, barite, and, to a lesser extent, sulfides. Rare earth element compositions along with fluid inclusion, halogen and isotopic data suggest that the fluorite barite mineralization and the spatially associated Eocene alkaline magmatism are petrogenetically unrelated, pointing instead to the regional circulation of hydrothermal basinal brines mixed to various degrees with meteoric water in a dominantly closed rock-buffered system at progressively higher temperatures and fluid/rock ratios. In this respect, fluid inclusion microthermometric measurements show that the ore-bearing hydrothermal system developed in two separate stages of fluorite-barite mineralization, as also revealed by isotopic data. Both stages precipitated from saline fluids at shallow crustal levels (i.e., 〈5 km), and were related, in varying degrees, to different stages of basin evolution and salt dome growth (salt mobilization and mineralization). During the first stage, the ore fluid was a highly saline aqueous brine with a total salinity up to 44.2 wt % NaCl + KCl equiv, at temperatures ≥82°C and possibly up to 218°C, whereas in the second stage the mineralizing fluid had a similar temperature range, but lower salinities (~20–10 wt % NaCl equiv). The recorded high salinities are interpreted to represent the involvement of a mixture of halite dissolution water and evaporated seawater component. Oxygen ( 18 O = 21.7 to 29.6 V-SMOW) and carbon ( 13 C = –7.9 to 0.2 V-PDB) isotope data along with strontium ( 87 Sr/ 86 Sr = 0.70300–070789) and lead ( 206 Pb/ 204 Pb = 17.961–20.96, 207 Pb/ 204 Pb = 15.511–15.697, 208 Pb/ 204 Pb = 37.784–39.993) isotope ratios suggest the involvement of a mixture of oil-bearing fluids, basinal brines, and meteoric fluids that interacted extensively with the early Jurassic host carbonates, the underlying Triassic salt-bearing diapir, associated siliciclastic rocks, and the highly fractionated and greisenized Hercynian granitic crystalline basement, resulting in the release of fluoride, metals, and other constituents to form the Jbel Tirremi deposit. Petroleum-bearing fluid, released from overpressured portions of the Guercif Basin at lithostatic pressures, and bittern brines dominated the first stage of mineralization. Mixing of saline, oxidized, CaCl 2 - and sulfate-rich bittern brine with oil-bearing fluid resulted in fluorite precipitation of stage I. Conversely, during the second stage of mineralization, the hydrothermal system was open to the influx of oxidized meteoric water as a consequence of the upward migration of the Triassic salt-bearing diapir and associated pressure decrease. The shift from stage I to stage II is associated with the evolution of the system from lithostatic to mostly hydrostatic pressure conditions. Stage I mineralization is thought to have occurred during the Late Miocene in response to rapid sedimentation and high subsidence rates and subsequent hydrocarbon migration associated with the outward migration of the Rif thrust front. Conversely, stage II mineralization occurred coevally with the uplift phase during Tortonian time.

Description: High-grade iron ore of the 4EE orebody of the 4E deposit (〉200 Mt at 63.5 wt % Fe) occurs as a southerly dipping sheet within banded iron formation (BIF) of the Paleoproterozoic Dales Gorge and Joffre members of the Brockman Iron Formation. Structural reconstruction of the 4E deposit shows that reactivation of the 18E fault and development of the NW-striking, steeply SW dipping 4E and 4EE normal faults resulted in preservation of the 4EE orebody below the 4E deposit, and 400 m below the modern topographic surface. Three hypogene alteration zones between low-grade BIF and high-grade iron ore are observed: (1) distal magnetite-quartz-dolomite-stilpnomelane-hematite ± pyrite, (2) intermediate magnetite-dolomite-hematite-chlorite-quartz-stilpnomelane, and (3) proximal hematite-dolomite-chlorite ± pyrite ± magnetite. Hydrothermal alteration is temporally and spatially constrained by NW-trending dolerite dikes that intruded the 4E and 4EE faults prior to hypogene alteration. Six vein types (V 1 –V 6 ) are recognized at the 4E deposit. The veins both cut and parallel the primary BIF layers and were emplaced contemporaneously with the hydrothermal alteration zones that record the transformation of low-grade BIF to high-grade iron ore. Our integrated structural-hydrothermal alteration and fluid flow model proposes that during early stage 1a, hypogene fluid flow in the 4E orebody occurred during a period of continental extension and enhanced heat flow within sedimentary basins to the south of the Paraburdoo Range. Heated basinal brines were focused by the NW-striking, steeply SW dipping 4E and 4EE normal faults and reacted with BIF of the Dales Gorge and Joffre members. The warm to hot (160°–255°C), Ca-rich (26.6–31.9 equiv wt % CaCl 2 ) basinal brine interacted with magnetite-chert layers, transforming them into magnetite-quartz-dolomite-stilpnomelane-hematite-pyrite BIF. The iron-rich brine (up to 2.8 wt % Fe) likely originated from evaporated seawater that had lost Mg and Na and gained Li and Ca through fluid-rock reactions with volcaniclastic rocks and carbonate successions within the Wittenoom Formation. The first incursion of deeply circulating, low-salinity (5.8–9.5 wt % NaCl equiv), heated (106°–201°C) modified meteoric water is recorded in late stage 1a minerals. This modified meteoric water had lost some of its Na through wall rock interaction with plagioclase, possibly by interaction with dolerite of the Weeli Wooli Formation that directly overlies the Joffre and Dales Gorge members. Stage 1b involved continuing reactions between the hydrothermal fluids and the magnetite-quartz-dolomite-stilpnomelane-hematite-pyrite BIF, and produced both the intermediate magnetite-dolomite-hematite-chlorite-pyrite and the proximal hematite-dolomite-magnetite-stilpnomelane alteration assemblages. Microplaty (10–80 μ m), platy (100–250 μ m), and anhedral hematite increasingly replace magnetite in the intermediate alteration zone, forming the proximal alteration zones that consist of microplaty, platy, anhedral hematite and magnetite. The intermediate and proximal alteration zones represent the mixing of a hot (250°–400°C), high-salinity, Ca-rich (30–40 wt % CaCl 2 equiv), Sr-rich basinal brine with low-temperature and low-salinity (~5 wt % NaCl equiv) modified meteoric water that was heated (~100°–200°C) during its descent into the upper crust. Heterogeneous mixing of the two end-member fluids resulted in the trapping of primary fluid inclusion assemblages containing a wide range of trapping temperatures (up to 200°C) and salinities (up to 25 wt % NaCl equiv). Stage 1c of the hypogene hydrothermal fluid is characterized by low-temperature (〈110°C), low-salinity (~5 wt % NaCl) meteoric water that interacted with the proximal hematite-dolomite-magnetite-stilpnomelane–altered BIF, leaving a porous, hematite-apatite high-grade ore. Supergene alteration affected the orebody since the Cretaceous and produced a hematite-goethite alteration assemblage, resulting in destruction of the hypogene alteration zones that are only preserved below the depth of modern weathering. Discovery of the concealed 4EE orebody of the 4E deposit demonstrates that structural geology plays a critical role in the exploration for high-grade iron orebodies. Structural reconstruction should be considered a critical exploration activity in structurally complex terranes where concealed orebodies may exist.

Description: Sea-floor imagery, volcanic rock, massive sulfide, and hydrothermal plume samples ( 3 He, pH, dissolved Fe and Mn, and particulate chemistry) have been collected from the Rumble II West volcano, southern Kermadec arc, New Zealand. Rumble II West is a caldera volcano with an ~3-km-diameter summit depression bounded by ring faults with a resurgent central cone. Rocks recovered to date are predominantly mafic in composition (i.e., basalt to basaltic andesite) with volumetrically lesser intermediate rocks (i.e., andesite). On the basis of its size, geometry, volcanic products, and composition, Rumble II West can be classified as a mafic caldera volcano. Rumble II West has a weak hydrothermal plume signature characterized by a small but detectable 3 He anomaly (25%). Time-series light scattering data though, obtained from vertical casts and tow-yos, do show that hydrothermal activity has increased in intensity between 1999 and 2011. Massive sulfides recovered from the eastern caldera wall and eastern flank of the central cone are primarily comprised of barite and chalcopyrite, with lesser sphalerite, pyrite, and traces of galena. The weak hydrothermal plume signal indicates that the volcano is in a volcanic-hydrothermal quiescent stage compared to other volcanoes along the southern Kermadec arc, although the preponderance of barite with massive sulfide mineralization indicates higher temperature venting in the past. Of the volcanoes along the Kermadec-Tonga arc known to host massive sulfides (i.e., Clark, Rumble II West, Brothers, Monowai, Volcano 19, and Volcano 1), the majority (five out of six) are dominantly mafic in composition and all but one of these mafic volcanoes form moderate-size to large calderas. To date, mafic calderas have been largely ignored as hosts to sea-floor massive sulfide deposits. That 75% of the presently known massive sulfide-bearing calderas along the arc are mafic in composition (the dacitic Brothers volcano is the exception) has important implications for sea-floor massive sulfide mineral exploration in the modern oceans and ancient rock record on land.

Description: The Monowai volcanic center is located at the midpoint along the ~2,530-km-long Tonga-Kermadec arc system. The Monowai volcanic center is comprised of a large elongate caldera (Monowai caldera area ~35 km 2 ; depth to caldera floor 1,590 m), which has formed within an older caldera some 84 km 2 in area. To the south of this nested caldera system is a large composite volcano, Monowai cone, which rises to within ~100 m of the sea surface and which has been volcanically active for the past several decades. Mafic volcanic rocks dominate the Monowai volcanic center; basalts are the most common rock type recovered from the cone, whereas basaltic andesites are common within the caldera. Hydrothermal plume mapping has shown at least three major hydrothermal systems associated with the caldera and cone: (1) the summit of the cone, (2) low-temperature venting (〈60°C; Mussel Ridge) on the southwestern wall of the caldera, and (3) a deeper caldera source with higher temperature venting that has yet to be observed. The cone summit plume shows large anomalies in pH (a shift of –2.00 pH units) and 3 He (≤358%), and noticeable H 2 S (up to 32 μ m), and CH 4 (up to 900 nm). The summit plume is also metal rich, with elevated total dissolvable Fe (TDFe up to 4,200 nm), TDMn (up to 412 nm), and TDFe/TDMn (up to 20.4). Particulate samples have elevated Fe, Si, Al, and Ti consistent with addition to the hydrothermal fluid from acidic water-rock reaction. Plumes extending from ~1,000- to 1,400-m depth provide evidence for a major hydrothermal vent system in the caldera. The caldera plume has lower values for TDFe and TDMn, although some samples show higher TDMn concentrations than the cone summit plume; caldera plume samples are also relatively gas poor (i.e., no H 2 S detected, pH shift of –0.06 pH units, CH 4 concentrations up to 26 nm). The composition of the hydrothermal plumes in the caldera have higher metal contents than the sampled vent fluids along Mussel Ridge, requiring that the source of the caldera plumes is at greater depth and likely of higher temperature. Minor plumes detected as light scattering anomalies but with no 3 He anomalies down the northern flank of the Monowai caldera most likely represent remobilization of volcanic debris from the volcano flanks. We believe the Monowai volcanic center is host to a robust magmatic-hydrothermal system, with significant differences in the style and composition of venting at the cone and caldera sites. At the cone, the large shifts in pH, very high 3 He% values, elevated TDFe and TDFe/TDMn, and the H 2 S- and CH 4 -rich nature of the plume fluids, together with elevated Ti, P, V, S, and Al in hydrothermal particulates, indicates significant magmatic volatile ± metal contributions in the hydrothermal system coupled with aggressive acidic water-rock interaction. By contrast, the caldera has low TDFe/TDMn in hydrothermal plumes; however, elevated Al and Ti contents in caldera particulate samples, combined with the presence of alunite, pyrophyllite, sulfide minerals, and native sulfur in samples from Mussel Ridge suggest past, and perhaps recent, acid volatile-rich venting and active Fe sulfide formation in the subsurface.

Description: Aeromagnetic data are used to better understand the geology and mineral resources near the Late Cretaceous Pebble porphyry Cu-Au-Mo deposit in southwestern Alaska. The reduced-to-pole (RTP) transformation of regional-scale aeromagnetic data shows that the Pebble deposit is within a cluster of magnetic anomaly highs. Similar to Pebble, the Iliamna, Kijik, and Neacola porphyry copper occurrences are in magnetic highs that trend northeast along the crustal-scale Lake Clark fault. A high-amplitude, short- to moderate-wavelength anomaly is centered over the Kemuk occurrence, an Alaska-type ultramafic complex. Similar anomalies are found west and north of Kemuk. A moderate-amplitude, moderate-wavelength magnetic low surrounded by a moderate-amplitude, short-wavelength magnetic high is associated with the gold-bearing Shotgun intrusive complex. The RTP transformation of the district-scale aeromagnetic data acquired over Pebble permits differentiation of a variety of Jurassic to Tertiary magmatic rock suites. Jurassic-Cretaceous basalt and gabbro units and Late Cretaceous biotite pyroxenite and granodiorite rocks produce magnetic highs. Tertiary basalt units also produce magnetic highs, but appear to be volumetrically minor. Eocene monzonite units have associated magnetic lows. The RTP data do not suggest a magnetite-rich hydrothermal system at the Pebble deposit. The 10-km upward continuation transformation of the regional-scale data shows a linear northeast trend of magnetic anomaly highs. These anomalies are spatially correlated with Late Cretaceous igneous rocks and in the Pebble district are centered over the granodiorite rocks genetically related to porphyry copper systems. The spacing of these anomalies is similar to patterns shown by the numerous porphyry copper deposits in northern Chile. These anomalies are interpreted to reflect a Late Cretaceous magmatic arc that is favorable for additional discoveries of Late Cretaceous porphyry copper systems in southwestern Alaska.

Description: The Spotted Quoll PGE-bearing Ni deposit in the Forrestania greenstone belt in the Archean Yilgarn block in Western Australia is a komatiite-associated massive sulfide orebody tectonically displaced from its original host. The brecciated ore contains clasts of quartz and garnet schist and is located along a shear zone overlain by banded iron formation (BIF) and underlain by BIF and quartz-biotite metasediments. The deformation of the ore has destroyed its magmatic textures and it has been sheared and recrystallized at amphibolite facies. Then the deformed ore has been subjected to a hydrothermal event that concentrated the PGE with Au and As, often at the edge of the Ni ore. The PGE are distributed between PGM and in solid solution in Ni sulfarsenides, and Pd also occurs in pentlandite. The PGM include sudburyite (PdSb), sperrylite (PtAs 2 ), and irarsite (IrAsS). All six PGE and minor Au are hosted in gersdorffite (NiAsS). Two generations of gersdorffite have been recognized. A higher temperature magmatic euhedral Co-rich gersdorffite encloses Ir-, Pt- and Rh-bearing PGM surrounded by halos of Rh-, Ir-, and Os-rich gersdorffite. A lower temperature Ni-rich gersdorffite forms anhedral grains and rims on grains of nickeline (NiAs). In this low-temperature gersdorffite PGE are concentrated toward the mineral edges. Sudburyite and gold occur associated predominantly with nickeline. The PGE and gold are now predominantly associated with sulfarsenides that are the controlling factor for their distribution.

Description: Equilibration between sulfide liquid and olivine is expressed in terms of the exchange coefficient for Fe and Ni, K D = (X NiS /X FeS ) sulfide_liquid /(X NiO /X FeO ) olivine . The positive dependence of K D on Ni + Cu content of sulfide liquid, as well as on f O 2 , has been demonstrated experimentally and gives rise to a critical nonlinearity in the relationship between sulfide and olivine-saturated silicate liquid compositions. Measured K D values for olivine-sulfide pairs from disseminated magmatic sulfide ores at Betheno (Western Australia) and Mirabela (Brazil) are consistent with independent estimates of f O 2 , and fall within the range where the composition dependence of K D is strong. This effect has been modeled quantitatively, using an empirical best fit to available experimental data as a parameterization of the K D variability, and calculating the equilibrium distribution of Fe, Ni, and Mg between coexisting olivine, silicate melt, and sulfide liquid as a function of the silicate/sulfide mass ratio R. It is shown that the composition dependence of K D is a key factor in giving rise to extremely Ni rich sulfides as exemplified by Betheno and Mirabela, where coexisting olivine is also Ni rich. Highly Ni enriched sulfides with anomalously high Ni/Cu ratios may be more common in nature than is commonly recognized and do not need to be explained by hydrothermal alteration processes.

Description: Laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) spot analysis and element mapping coupled with high-resolution focused ion beam-scanning electron microscopy (FIB-SEM) imaging has been performed on Au-hosting sulfides from a Proterozoic orogenic gold deposit, Tanami gold province, north-central Australia. Gold distribution patterns in the arsenopyrite-pyrite assemblage, which probably crystallized toward the end of the Au-forming event, suggest a process of initial scavenging of Au into arsenopyrite and subsequent remobilization of that Au following brittle fracture. Gold expelled from the sulfide lattice during the remobilization event is reconcentrated around the margins of the same arsenopyrite grains and within swarms of crosscutting microfractures. The distribution of Pb, Bi, and Ag closely mimic Au, indicating that these elements were also reconcentrated. Preservation of oscillatory zonation patterns for Co, Ni, Sb, Se, and Te in arsenopyrite imply, however, that no significant degree of sulfide recrystallization took place. Residual concentrations of invisible gold (in grain centers) are 〈5 ppm in arsenopyrite and 〈1 ppm in coexisting pyrite. The presence of submicron-sized pores is suggestive of a fluid-driven process rather than solid state diffusion. Micron-scale (2–10 μ m) remobilized gold is accompanied by fine particles (200 nm–2 μ m) and nanoparticles (〈200 nm) of gold. The extensive variation of Au concentrations within single arsenopyrite grains underlines the significance of textures when using trace element data to understand how gold ores evolved.