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At least 37 records · Page 2Linked to original sources
USGS2008

Gold deposits and occurrences of the Greater Caucasus, Georgia Republic: Their genesis and prospecting criteria

The south-central part of the Greater Caucasus region, Georgia Republic, represents an extremely prospective region for significant orogenic gold deposits. Gold-bearing quartz veins are concentrated in two extensive WNW-trending belts, the Mestia-Racha and Svaneti districts, within the northern margin of the Southern Slope Zone of the Great Caucasus orogen. This metalliferous region is dominated by Early to Middle Jurassic slates, which are part of a terrane that likely accreted to the continental margin from late Paleozoic to Jurassic. The slates were subsequently intruded by both Middle to Late Jurassic and Neogene granitoids. Quartz veins in the more carbonaceous slate units are most consistently enriched in As, Au, Hg, Sb, and W, and show mineralization styles most consistent with typical orogenic gold deposits. Quartz veins in the Mestia-Racha district were mined in Soviet times for As, Sb, and W, but many of these are now being recognized as gold resource targets. The veins occur in the footwall of a thrust fault between the Southern Slope zone and an earlier accreted terrane, the Main Zone, to the north. Many veins in the district continue along strike for > 1??km and some cut Neogene intrusions, constraining ore formation to the most recent 4 to 5??million years. Gold deposition thus correlates with final collision of the Arabian plate to the south and uplift of the ore-hosting Greater Caucasus. The Zopkhito deposit, previously mined for antimony, contains an estimated 55??t Au at a cutoff grade of 0.5??g/t. The veins are localized in an area where smaller-order structures show a major change in strike from N-S to more E-W trends. A pyrite-arsenopyrite ore stage includes gold concentrated in both sulfide phases; it is overprinted by a later stibnite-dominant stage. Fluid-inclusion studies of ore samples from the Zopkhito deposit indicate minimum trapping temperatures of 300 to 350????C and 200 to 300????C for the two stages, respectively, and minimum trapping pressures of 0.2 to 0.5??kbar. Ore-forming fluids, with approximately 5 to 20??mol% non-aqueous gas, evolved from N2-dominant to CO2-dominant during evolution of the hydrothermal system. ??34S values of + 1 to + 4??? for ore-related sulfides at Zopkhito are consistent with a sedimentary rock source for the sulfur, and ??18O quartz measurements of 16 to 21??? are consistent with either a magmatic or metamorphic fluid. More than 60 gold-bearing lodes and placers in the Svaneti district occur along the thrust between the Southern Slope and Main Zones. Lode gold potential was first recognized in the historic placer district in the 1980s, with many auriferous quartz veins cutting Middle Jurassic igneous rocks. Brecciated veins in the 18??t Au Lukhra deposit cut a small granodioritic to dioritic stock; the latter intrudes Devonian schist immediately north of the thrust. Presently, there are three recognized ore zones in the deposit, with the most significant occurring over an area 140??m in length and 12??m-wide, with typical grades of 7 to 9??g/t Au. Reconnaissance fluid-inclusion studies of ore samples from the Lukhra deposit indicate minimum trapping temperatures of 220????C. Measurements of ??18Oquartz of about 10??? suggest buffering of isotopic composition by the igneous host rocks.

Ore Geology Reviews↗
USGS2011

Magmatic-vapor expansion and the formation of high-sulfidation gold deposits: Structural controls on hydrothermal alteration and ore mineralization

High-sulfidation copper–gold lode deposits such as Chinkuashih, Taiwan, Lepanto, Philippines, and Goldfield, Nevada, formed within 1500 m of the paleosurface in volcanic terranes. All underwent an early stage of extensive advanced argillic silica–alunite alteration followed by an abrupt change to spatially much more restricted stages of fracture-controlled sulfide–sulfosalt mineral assemblages and gold–silver mineralization. The alteration as well as ore mineralization stages of these deposits were controlled by the dynamics and history of syn-hydrothermal faulting. At the Sulfate Stage, aggressive advanced argillic alteration and silicification were consequent on the in situ formation of acidic condensate from magmatic vapor as it expanded through secondary fracture networks alongside active faults. The reduction of permeability at this stage due to alteration decreased fluid flow to the surface, and progressively developed a barrier between magmatic-vapor expansion constrained by the active faults and peripheral hydrothermal activity dominated by hot-water flow. In conjunction with the increased rock strength resulting from alteration, subsequent fault-slip inversion in response to an increase in compressional stress generated new, highly permeable fractures localized by the embrittled, altered rock. The new fractures focused magmatic-vapor expansion with much lower heat loss so that condensation occurred. Sulfide Stage sulfosalt, sulfide, and gold–silver deposition then resulted from destabilization of vapor phase metal species due to vapor decompression through the new fracture array. The switch from sulfate to sulfide assemblages is, therefore, a logical consequence of changes in structural permeability due to the coupling of alteration and fracture dynamics rather than to changes in the chemistry of the fluid phase at its magmatic source.

Ore Geology Reviews↗
USGS2011

Effects of intrusions on grades and contents of gold and other metals in volcanogenic massive sulfide deposits

The reason some VMS deposits contain more gold or other metals than others might be due to the influence of intrusions. A new approach examining this possibility is based on examining the information about many VMS deposits to test statistically if those with associated intrusions have significantly different grades or amounts of metals. A set of 632 VMS deposits with reported grades, tonnages, and information about the observed presence or absence of subvolcanic or plutonic intrusive bodies emplaced at or after VMS mineralization is statistically analyzed. Deposits with syn-mineralization or post-mineralization intrusions nearby have higher tonnages than deposits without reported intrusions, but the differences are not statistically significant. When both kinds of intrusions are reported, VMS deposit sizes are significantly higher than in the deposits without any intrusions. Gold, silver, zinc, lead, and copper average grades are not significantly different in the VMS deposits with nearby intrusions compared to deposits without regardless of relative age of intrusive. Only zinc and copper contents are significantly higher in VMS deposits with both kinds of intrusive reported. These differences in overall metal content are due to significantly larger deposit sizes of VMS deposits where both intrusive kinds are observed and reported, rather than any difference in metal grades.

Ore Geology Reviews↗
USGS2015

Critical metals in manganese nodules from the Cook Islands EEZ, abundances and distributions

The Cook Islands (CIs) Exclusive Economic Zone (EEZ) encompasses 1,977,000 km 2 and includes the Penrhyn and Samoa basins abyssal plains where manganese nodules flourish due to the availability of prolific nucleus material, slow sedimentation rates, and strong bottom currents. A group of CIs nodules was analyzed for mineralogical and chemical composition, which include many critical metals not before analyzed for CIs nodules. These nodules have varying sizes and nuclei material; however all are composed predominantly of δ-MnO 2 and X-ray amorphous iron oxyhydroxide. The mineralogy, Fe/Mn ratios, rare earth element contents, and slow growth rates (mean 1.9 mm/10 6 years) reflect formation primarily by hydrogenetic precipitation. The paucity of diagenetic input can be explained by low primary productivity at the surface and resultant low organic matter content in seafloor sediment, producing oxic seafloor and sub-seafloor environments. The nodules contain high mean contents of Co (0.41%), Ni (0.38%), Ti (1.20%), and total rare earth elements plus yttrium (REY; 0.167%), and also high contents of Mo, Nb, V, W, and Zr. Compiled data from a series of four cruises by the Japan International Cooperation Agency and the Mining agency of Japan from 1985 to 2000 were used to generate a map that defines the statistical distribution of nodule abundance throughout the EEZ, except the Manihiki Plateau. The abundance distribution map shows a belt of high nodule abundance (19–45 kg/m 2 ) that starts in the southeast corner of the EEZ, runs northwest, and also bifurcates into a SW trending branch. Small, isolated areas contain abundances of nodules of up to 58 kg/m 2 . Six ~ 20,000 km 2 areas of particularly high abundance were chosen to represent potential exploration areas, and maps for metal concentration were generated to visualize metal distribution and to extrapolate estimated metal tonnages within the six sites and the EEZ as a whole. Grades for Mn, Cu, and Ni are low in CIs nodules in areas of high abundance; however, Ti, Co, and REY show high contents where nodule abundances are high. Of the six areas identified to represent a range of metal contents, one at the northern end of the N-S abundance main belt optimizes the most metals and would yield the highest dry metric tons for Mn (61,002,292), Ni (1,247,834), Mo (186,166), V (356,247), W (30,215), and Zr (195,323). When compared with the Clarion–Clipperton Zone, the CIs nodules show higher nodule abundances (> 25 kg/m 2 over ~ 123,844 km 2 ), and are more enriched in the green-tech, high-tech, and energy metals Co, Ti, Te, Nb, REY, Pt, and Zr. The CIs EEZ shows a significant resource potential for these critical metals due to their high prices, high demand, and the high nodule abundance, which will allow for a smaller footprint for a 20-year mine site and therefore smaller environmental impact.

Ore Geology Reviews↗
USGS2017

Genetic and grade and tonnage models for sandstone-hosted roll-type uranium deposits, Texas Coastal Plain, USA

The coincidence of a number of geologic and climatic factors combined to create conditions favorable for the development of mineable concentrations of uranium hosted by Eocene through Pliocene sandstones in the Texas Coastal Plain. Here 254 uranium occurrences, including 169 deposits, 73 prospects, 6 showings and 4 anomalies, have been identified. About 80 million pounds of U 3 O 8 have been produced and about 60 million pounds of identified producible U 3 O 8 remain in place. The development of economic roll-type uranium deposits requires a source, large-scale transport of uranium in groundwater, and deposition in reducing zones within a sedimentary sequence. The weight of the evidence supports a source from thick sequences of volcanic ash and volcaniclastic sediment derived mostly from the Trans-Pecos volcanic field and Sierra Madre Occidental that lie west of the region. The thickest accumulations of source material were deposited and preserved south and west of the San Marcos arch in the Catahoula Formation. By the early Oligocene, a formerly uniformly subtropical climate along the Gulf Coast transitioned to a zoned climate in which the southwestern portion of Texas Coastal Plain was dry, and the eastern portion humid. The more arid climate in the southwestern area supported weathering of volcanic ash source rocks during pedogenesis and early diagenesis, concentration of uranium in groundwater and movement through host sediments. During the middle Tertiary Era, abundant clastic sediments were deposited in thick sequences by bed-load dominated fluvial systems in long-lived channel complexes that provided transmissive conduits favoring transport of uranium-rich groundwater. Groundwater transported uranium through permeable sandstones that were hydrologically connected with source rocks, commonly across formation boundaries driven by isostatic loading and eustatic sea level changes. Uranium roll fronts formed as a result of the interaction of uranium-rich groundwater with either (1) organic-rich debris adjacent to large long-lived fluvial channels and barrier–bar sequences or (2) extrinsic reductants entrained in formation water or discrete gas that migrated into host units via faults and along the flanks of salt domes and shale diapirs. The southwestern portion of the region, the Rio Grande embayment, contains all the necessary factors required for roll-type uranium deposits. However, the eastern portion of the region, the Houston embayment, is challenged by a humid environment and a lack of source rock and transmissive units, which may combine to preclude the deposition of economic deposits. A grade and tonnage model for the Texas Coastal Plain shows that the Texas deposits represent a lower tonnage subset of roll-type deposits that occur around the world, and required aggregation of production centers into deposits based on geologic interpretation for the purpose of conducting a quantitative mineral resource assessment.

Texas↗
USGS2017

Undiscovered porphyry copper resources in the Urals—A probabilistic mineral resource assessment

A probabilistic mineral resource assessment of metal resources in undiscovered porphyry copper deposits of the Ural Mountains in Russia and Kazakhstan was done using a quantitative form of mineral resource assessment. Permissive tracts were delineated on the basis of mapped and inferred subsurface distributions of igneous rocks assigned to tectonic zones that include magmatic arcs where the occurrence of porphyry copper deposits within 1 km of the Earth's surface are possible. These permissive tracts outline four north-south trending volcano-plutonic belts in major structural zones of the Urals. From west to east, these include permissive lithologies for porphyry copper deposits associated with Paleozoic subduction-related island-arc complexes preserved in the Tagil and Magnitogorsk arcs, Paleozoic island-arc fragments and associated tonalite-granodiorite intrusions in the East Uralian zone, and Carboniferous continental-margin arcs developed on the Kazakh craton in the Transuralian zone. The tracts range from about 50,000 to 130,000 km 2 in area. The Urals host 8 known porphyry copper deposits with total identified resources of about 6.4 million metric tons of copper, at least 20 additional porphyry copper prospect areas, and numerous copper-bearing skarns and copper occurrences. Probabilistic estimates predict a mean of 22 undiscovered porphyry copper deposits within the four permissive tracts delineated in the Urals. Combining estimates with established grade and tonnage models predicts a mean of 82 million metric tons of undiscovered copper. Application of an economic filter suggests that about half of that amount could be economically recoverable based on assumed depth distributions, availability of infrastructure, recovery rates, current metals prices, and investment environment.

Urals↗
USGS2017

Origin and evolution of mineralizing fluids and exploration of the Cerro Quema Au-Cu deposit (Azuero Peninsula, Panama) from a fluid inclusion and stable isotope perspective

Cerro Quema is a high sulfidation epithermal Au-Cu deposit with a measured, indicated and inferred resource of 35.98 Mt. @ 0.77 g/t Au containing 893,600 oz. Au (including 183,930 oz. Au equiv. of Cu ore). It is characterized by a large hydrothermal alteration zone which is interpreted to represent the lithocap of a porphyry system. The innermost zone of the lithocap is constituted by vuggy quartz with advanced argillic alteration locally developed on its margin, enclosed by a well-developed zone of argillic alteration, grading to an external halo of propylitic alteration. The mineralization occurs in the form of disseminations and microveinlets of pyrite, chalcopyrite, enargite, tennantite, and trace sphalerite, crosscut by quartz, barite, pyrite, chalcopyrite, sphalerite and galena veins. Microthermometric analyses of two phase (L + V) secondary fluid inclusions in igneous quartz phenocrysts in vuggy quartz and advanced argillically altered samples indicate low temperature (140–216 °C) and low salinity (0.5–4.8 wt% NaCl eq.) fluids, with hotter and more saline fluids identified in the east half of the deposit (Cerro Quema area). Stable isotope analyses (S, O, H) were performed on mineralization and alteration minerals, including pyrite, chalcopyrite, enargite, alunite, barite, kaolinite, dickite and vuggy quartz. The range of δ 34 S of sulfides is from − 4.8 to − 12.7‰, whereas δ 34 S of sulfates range from 14.1 to 17.4‰. The estimated δ 34 S ΣS of the hydrothermal fluid is − 0.5‰. Within the advanced argillic altered zone the δ 34 S values of sulfides and sulfates are interpreted to reflect isotopic equilibrium at temperatures of ~ 240 °C. The δ 18 O values of vuggy quartz range from 9.0 to 17.5‰, and the δ 18 O values estimated for the vuggy quartz-forming fluid range from − 2.3 to 3.0‰, indicating that it precipitated from mixing of magmatic fluids with surficial fluids. The δ 18 O of kaolinite ranges from 12.7 to 18.1‰ and δD from − 103.3 to − 35.2‰, whereas the δ 18 O of dickite varies between 12.7 and 16.3‰ and δD from − 44 to − 30. Based on δ 18 O and δD, two types of kaolinite/dickite can be distinguished, a supergene type and a hypogene type. Combined, the analytical data indicate that the Cerro Quema deposit formed from magmatic-hydrothermal fluids derived from a porphyry copper-like intrusion located at depth likely towards the east of the deposit. The combination of stable isotope geochemistry and fluid inclusion analysis may provide useful exploration vectors for porphyry copper targets in the high sulfidation/lithocap environment.

Azuero Peninsula↗
USGS2017

Formation of Fe-Mn crusts within a continental margin environment

This study examines Fe-Mn crusts that form on seamounts along the California continental-margin (CCM), within the United States 200 nautical mile exclusive economic zone. The study area extends from approximately 30° to 38° North latitudes and from 117° to 126° West longitudes. The area of study is a tectonically active northeast Pacific plate boundary region and is also part of the North Pacific Subtropical Gyre with currents dominated by the California Current System. Upwelling of nutrient-rich water results in high primary productivity that produces a pronounced oxygen minimum zone. Hydrogenetic Fe-Mn crusts forming along the CCM show distinct chemical and mineral compositions compared to open-ocean crusts. On average, CCM crusts contain more Fe relative to Mn than open-ocean Pacific crusts. The continental shelf and slope release both Fe and Mn under low-oxygen conditions. Silica is also enriched relative to Al compared to open-ocean crusts. This is due to the North Pacific silica plume and enrichment of Si along the path of deep-water circulation, resulting in Si enrichment in bottom and intermediate waters of the eastern Pacific. The CCM Fe-Mn crusts have a higher percentage of birnessite than open-ocean crusts, reflecting lower dissolved seawater oxygen that results from the intense coastal upwelling and proximity to zones of continental slope pore-water anoxia. Carbonate fluorapatite (CFA) is not present and CCM crusts do not show evidence of phosphatization, even in the older sections. The mineralogy indicates a suboxic environment under which birnessite forms, but in which pH is not high enough to facilitate CFA deposition. Growth rates of CCM crusts generally increase with increasing water depth, likely due to deep-water Fe sources mobilized from reduced shelf and slope sediments. Many elements of economic interest including Mn, Co, Ni, Cu, W, and Te have slightly or significantly lower concentrations in CCM crusts relative to crusts from the Pacific Prime Crust Zone and other open-ocean basins. However, concentrations of total rare earth elements and yttrium average only slightly lower contents and in the future may be a strategic resource for the U.S.

California↗
USGS2017

Re-Os systematics and geochemistry of cobaltite (CoAsS) in the Idaho cobalt belt, Belt-Purcell Basin, USA: Evidence for middle Mesoproterozoic sediment-hosted Co-Cu sulfide mineralization with Grenvillian and Cretaceous remobilization

We report the first study of the Re-Os systematics of cobaltite (CoAsS) using disseminated grains and massive sulfides from samples of two breccia-type and two stratabound deposits in the Co-Cu-Au Idaho cobalt belt (ICB), Lemhi subbasin to the Belt-Purcell Basin, Idaho, USA. Using a 185 Re + 190 Os spike solution, magnetic and non-magnetic fractions of cobaltite mineral separates give reproducible Re-Os analytical data for aliquot sizes of 150 to 200 mg. Cobaltite from the ICB has highly radiogenic 187 Os/ 188 Os ratios (17–45) and high 187 Re/ 188 Os ratios (600–1800) but low Re and total Os contents (ca. 0.4–4 ppb and 14–64 ppt, respectively). Containing 30 to 74% radiogenic 187 Os, cobaltite from the ICB is amenable to Re-Os age determination using the isochron regression approach. Re-Os data for disseminated cobaltite mineralization in a quartz-tourmaline breccia from the Haynes-Stellite deposit yield a Model 1 isochron age of 1349 ± 76 Ma (2σ, n = 4, mean squared weighted deviation MSWD = 2.1, initial 187 Os/ 188 Os ratio = 4.7 ± 2.2). This middle Mesoproterozoic age is preserved despite a possible metamorphic overprint or a pulse of metamorphic-hydrothermal remobilization of pre-existing cobaltite that formed along fold cleavages during the ca. 1190–1006 Ma Grenvillian orogeny. This phase of remobilization is tentatively identified by a Model 3 isochron age of 1132 ± 240 Ma (2σ, n = 7, MSWD = 9.3, initial 187 Os/ 188 Os ratio of 9.0 ± 2.9) for cobaltite in the quartz-tourmaline breccia from the Idaho zone in the Blackbird mine. All Mesoproterozoic cobaltite mineralization in the district was affected by greenschist- to lower amphibolite-facies (garnet zone) metamorphism during the Late Jurassic to Late Cretaceous Cordilleran orogeny. However, the fine- to coarse-grained massive cobaltite mineralization from the shear zone-hosted Chicago zone, Blackbird mine, is the only studied deposit that has severely disturbed Re-Os systematics with evidence for a linear trend of mixing with (metamorphic?) fluids. The new Re-Os ages and extremely high initial 187 Os/ 188 Os ratios of cobaltite reported here favor a magmatic-hydrothermal genetic model for a multi-stage REE-Y-Co-Cu-Au mineralization occurring at ca. 1370 to 1349 Ma, and related to the emplacement of the Big Deer Creek granite pluton at ca. 1377 Ma. In our model, deposition of paragenetically early xenotime and gadolinite was followed by an influx of Mesoproterozoic evaporitic brines and magmatic-hydrothermal fluids containing metals and reduced sulfur derived from mafic and oceanic island-arc Archean to Paleoproterozoic rocks in the Laurentian basement. Cobaltite mineralization occurred upon cooling of these fluids at an inferred temperature of 300 °C or below.

Idaho↗
USGS2017

Fractional crystallization-induced variations in sulfides from the Noril’sk-Talnakh mining district (polar Siberia, Russia)

The distribution of platinum-group elements (PGE) within zoned magmatic ore bodies has been extensively studied and appears to be controlled by the partitioning behavior of the PGE during fractional crystallization of magmatic sulfide liquids. However, other chalcophile elements, especially TABS (Te, As, Bi, Sb, and Sn) have been neglected despite their critical role in forming platinum-group minerals (PGM). TABS are volatile trace elements that are considered to be mobile so investigating their primary distribution may be challenging in magmatic ore bodies that have been somewhat altered. Magmatic sulfide ore bodies from the Noril’sk-Talnakh mining district (polar Siberia, Russia) offer an exceptional opportunity to investigate the behavior of TABS during fractional crystallization of sulfide liquids and PGM formation as the primary features of the ore bodies have been relatively well preserved. In this study, new petrographic (2D and 3D) and whole-rock geochemical data from Cu-poor to Cu-rich sulfide ores of the Noril’sk-Talnakh mining district are integrated with published data to consider the role of fractional crystallization in generating mineralogical and geochemical variations across the different ore types (disseminated to massive). Despite textural variations in Cu-rich massive sulfides (lenses, veins, and breccias), these sulfides have similar chemical compositions, which suggests that Cu-rich veins and breccias formed from fractionated sulfide liquids that were injected into the surrounding rocks. Numerical modeling using the median disseminated sulfide composition as the initial sulfide liquid composition and recent DMSS/liq and DISS/liq predicts the compositional variations observed in the massive sulfides, especially in terms of Pt, Pd, and TABS. Therefore, distribution of these elements in the massive sulfides was likely controlled by their partitioning behavior during sulfide liquid fractional crystallization, prior to PGM formation. Our observations indicate that in the Cu-poor massive sulfides the PGM formed as the result of exsolution from sulfide minerals whereas in the Cu-rich massive sulfides the PGM formed by crystallization from late-stage fractionated sulfide liquids. We suggest that the significant amount of Sn-bearing PGM may be related to crustal contamination from granodiorite, whereas As, Bi, Te, and Sb were likely added to the magma along with S from sedimentary rocks. Large PGM that are scarce and randomly distributed may account for most of the whole-rock Pt budget. Based on our results, we propose a holistic genetic model for the formation of the magmatic sulfide ore bodies of the Noril’sk-Talnakh mining district.

Siberia↗
USGS2017

Noble gas data from Goldfield and Tonopah epithermal Au-Ag deposits, ancestral Cascades Arc, USA: Evidence for a primitive mantle volatile source

The He, Ne, and Ar isotopic composition of fluid inclusions in ore and gangue minerals were analyzed to determine the source of volatiles in the high-grade Goldfield and Tonopah epithermal Au-Ag deposits in southwestern Nevada, USA. Ar and Ne are mainly atmospheric, whereas He has only a minor atmospheric component. Corrected 3 He/ 4 He ratios (with atmospheric He removed) range widely from 0.05 to 35.8 times the air 3 He/ 4 He ratio (R A ), with a median of 1.43 R A . Forty-one percent of measured 3 He/ 4 He ratios are ≥4 R A , corresponding to ≥50% mantle He assuming a mantle ratio of 8 R A . These results suggest that mafic magmas were part of the magmatic-hydrothermal system underlying Goldfield and Tonopah, and that associated mantle-sourced volatiles may have played a role in ore formation. The three highest corrected 3 He/ 4 He ratios of 17.0, 23.7, and 35.8 R A indicate a primitive mantle He source and are the highest yet reported for any epithermal-porphyry system and for the Cascades arc region. Compiled 3 He/ 4 He measurements from epithermal-porphyry systems in subduction-related magmatic arcs around the world (n = 209) display a statistically significant correlation between 3 He/ 4 He and Au-Ag grade. The correlation suggests that conditions which promote higher fluid inclusion 3 He/ 4 He ratios (abundance of mantle volatiles and focused upward volatile transport) have some relation to conditions that promote higher Au-Ag grades (focused flow of metal-bearing fluids and efficient chemical traps). Results of this and previous investigations of He isotopes in epithermal-porphyry systems are consistent with the hypothesis posed in recent studies that mafic magmas serve an important function in the formation of these deposits.

Cascades Arc↗
USGS2017

Element migration of pyrites during ductile deformation of the Yuleken porphyry Cu deposit (NW-China)

The strongly deformed Yuleken porphyry Cu deposit (YPCD) occurs in the Kalaxiangar porphyry Cu belt (KPCB), which occupies the central area of the Central Asian Orogenic Belt (CAOB) between the Sawu’er island arc and the Altay Terrane in northern Xinjiang. The YPCD is one of several typical subduction-related deposits in the KPCB, which has undergone syn-collisional and post-collisional metallogenic overprinting. The YPCD is characterized by three pyrite-forming stages, namely a hydrothermal stage A (Py I), a syn-ductile deformation stage B (Py II) characterized by Cu-Au enrichment, and a fracture-filling stage C (Py III). In this study, we conducted systematic petrographic and geochemical studies of pyrites and coexist biotite, which formed during different stages, in order to constrain the physicochemical conditions of the ore formation. Euhedral, fragmented Py I has low Pb and high Te and Se concentration and Ni contents are low with Co/Ni ratios mostly between 1 and 10 (average 9.00). Py I is further characterized by enrichments of Bi, As, Ni, Cu, Te and Se in the core relative to the rim domains. Anhedral round Py II has moderate Co and Ni contents with high Co/Ni ratios >10 (average 95.2), and average contents of 46.5 ppm Pb and 5.80 ppm Te. Py II is further characterized by decreasing Bi, Cu, Pb, Zn, Ag, Te, Mo, Sb and Au contents from the rim to the core domains. Annealed Py III has the lowest Co content of all pyrite types with Co/Ni ratios mostly <0.1 (average 1.33). Furthermore, Py III has average contents of 3.31 ppm Pb, 1.33 ppm Te and 94.6 ppm Se. In addition, Fe does not correlate with Cu and S in the Py I and Py III, while Py II displays a negative correlation between Fe and Cu as well as a positive correlation between Fe and S. Therefore, pyrites which formed during different tectonic regimes also have different chemical compositions. Biotite geothermometer and oxygen fugacity estimates display increasing temperatures and oxygen fugacities from stage A to stage B, while temperature and oxygen fugacities decrease from stage B to stage C. The Co/Ni ratio of pyrite depends discriminates between the different mineralizing stages in the Yuleken porphyry copper deposit: Py II, associated with the deformation stage B and Cu-enrichment, shows higher Co/Ni ratios and enrichments of Pb, Zn, Mo, Te and Sb than the pyrites formed during the other two stages. The Co/Ni ratio of pyrite can not only apply to discriminate the submarine exhalative, magmatic or sedimentary origins for ore deposits but also can distinguish different ore-forming stages in a single porphyry Cu deposit. Thus, Co/Ni ratio of pyrites may act as an important exploration tool to distinguish pyrites from Cu-rich versus barren area. Furthermore, the distribution of Cu, Mo, Pb, Au, Bi, Sb and Zn in the variably deformed pyrite is proportional to the extent of deformation of the pyrites, indicating in accordance with variable physicochemical conditions different element migration behavior during the different stages of deformation and, thus, mineralisation.

Ore Geology Reviews↗
USGS2017

Experimental investigation on thermochemical sulfate reduction in the presence of 1-pentanethiol at 200 and 250 °C: Implications for in situ TSR processes occurring in some MVT deposits

Organic sulfur compounds are ubiquitous in natural oil and gas fields and moderate-low temperature sulfide ore deposits. Previous studies have shown that organic sulfur compounds are important in enhancing the rates of thermochemical sulfate reduction (TSR) reactions, but the details of these reaction mechanisms remain unclear. In order to assess the extent of sulfate reduction in the presence of labile sulfur species at temperature conditions near to those where TSR occurs in nature, we conducted a series of experiments using the fused silica capillary capsule (FCSS) method. The tested systems containing labile sulfur species are MgSO 4 + 1-pentanethiol (C 5 H 11 SH) + 1-octene (C 8 H 16 ), MgSO 4 + 1-octene (C 8 H 16 ), MgSO 4 + 1-pentanethiol (C 5 H 11 SH), 1-pentanethiol (C 5 H 11 SH)+H 2 O, and MgSO 4 + 1-pentanethiol (C 5 H 11 SH) + ZnBr 2 systems. Our results show that: (1) intermediate oxidized carbon species (ethanol and acetic acid) are formed during TSR simulation experiments when 1-pentanethiol is present; (2) in the presence of ZnBr 2 , 1-pentanethiol can be oxidized by sulfate to CO 2 at 200 °C, which is within the temperature range observed in natural TSR; and (3) the precipitation of sulfide minerals may significantly promote the rate of TSR, indicating that the rates of in situ TSR reactions in ore deposits could be much faster than previously thought. This may be important for understanding the possibility of in situ TSR as a mechanism for the precipitation of metal sulfides in some ore deposits. These findings provide important experimental evidence for understanding the role of organic sulfur compounds in TSR reactions and the pathway of TSR reactions initiated by organic sulfur compounds under natural conditions.

Ore Geology Reviews↗
USGS2018

Intermediate sulfidation type base metal mineralization at Aliabad-Khanchy, Tarom-Hashtjin metallogenic belt, NW Iran

The Aliabad-Khanchy epithermal base metal deposit is located in the Tarom-Hashtjin metallogenic belt (THMB) of northwest Iran. The mineralization occurs as Cu-bearing brecciated quartz veins hosted by Eocene volcanic and volcaniclastic rocks of the Karaj Formation. Ore formation can be divided into five stages, with most ore minerals, such as pyrite and chalcopyrite being formed in the early stages. The main wall-rock alteration is silicification, and chlorite, argillic and propylitic alteration. Microthermometric measurements of fluid inclusion assemblages show that the ore-forming fluids have eutectic temperatures between −30 and −52 °C, trapping temperatures of 150–290 °C, and salinities of 6.6–12.4 wt% NaCl equiv. These data demonstrate that the ore-forming fluids were medium- to high-temperature, medium- to low-salinity, and low-density H 2 O–NaCl–CaCl 2 fluids. Calculated δ 18 O values indicate that ore-forming hydrothermal fluids had δ 18 O water ranging from +3.6‰ to +0.8‰, confirming that the ore–fluid system evolved from dominantly magmatic to dominantly meteoric. The calculated 34 S H2S values range from −8.1‰ to −5.0‰, consistent with derivation of the sulfur from either magma or possibly from local volcanic wall-rock. Combined, the fluid inclusion and stable isotope data indicate that the Aliabad-Khanchy deposit formed from magmatic-hydrothermal fluids. After rising to a depth of between 790 and 500 m, the fluid boiled and subsequent hydraulic fracturing may have led to inflow and/or mixing of early magmatic fluids with circulating groundwater causing deposition of base metals due to dilution and/or cooling. The Aliabad-Khanchy deposit is interpreted as an intermediate-sulfidation style of epithermal mineralization. Our data suggest that the mineralization at Aliabad-Khanchy and other epithermal deposits of the THMB formed by hydrothermal activity related to shallow late Eocene magmatism. The altered Eocene volcanic and volcaniclastic rocks, especially at the intersection of subvolcanic stocks with faults were the most favorable sites for epithermal ore bodies in the THMB.

Ore Geology Reviews↗
USGS2018

Two-event lode-ore deposition at Butte, USA: 40Ar/39Ar and U-Pb documentation of Ag-Au-polymetallic lodes overprinted by younger stockwork Cu-Mo ores and penecontemporaneous Cu lodes

The ore-genesis model for world-class deposits of the Butte mining district, Montana, USA, is deep pre-Main Stage porphyry Cu-Mo and overlying Main Stage Ag-Zn-Cu zoned-lode deposits, both of which formed from hydrothermal fluids driven by minor volumes of rhyolitic magma. The lode-specific model is that hydrothermal processes diminished in intensity outward from district center along lode veins, synchronously forming metal zones. The accepted models are controverted by new geologic and multi-method geochronologic studies. The new data reveal the following sequence of events: (1) Thermal study of country rock indicates that the 76.9-Ma Butte Granite cooled to 350–400 °C by 4 m.y. after emplacement. (2) Five quartz porphyry rhyolite dikes were emplaced at 67–65 Ma and another at 60 Ma (SHRIMP U-Pb) into the cooled Butte Granite without resetting 40 Ar/ 39 Ar ages in country rock. (3) Fifty-eight white mica and K-feldspar samples from alteration envelopes adjacent to Ag-Au-polymetallic lodes in outer parts of the district, Zn-rich lodes in intermediate parts, and Cu-rich lodes in the district center yield 40 Ar/ 39 Ar ages of 73–70 Ma for Ag-rich lodes, 65–64 Ma for Cu-rich lodes, and complex age spectra of 69–65 Ma for Zn-rich lodes. The data show that Ag-Au-polymetallic lodes occupied cross-district fractures by about 73 Ma, forming the greater Butte mining district. At 67–65 Ma, minor quartz porphyry dikes were emplaced into central and eastern parts of the rejuvenated fracture system but without evidence of related cupola or volcanic rocks or of thermal disturbance in the country rock. At 64.5 Ma, overlapping hydrothermal cells formed two stockwork Cu-Mo domes in deep parts of the fracture system. At 65–64 Ma and closely related to late-stage stockwork Cu-Mo activity, a penecontemporaneous hydrothermal pulse formed a high-sulfidation hydrothermal plume that (1) utilized the large re-opened fractures to cannibalize and remobilize Cu from autologous, stockwork, and older Ag-Au-polymetallic lodes, (2) deposited the rich, high-sulfidation Cu lodes, and (3) mobilized metals from early Ag-Au-polymetallic veins in middle parts of the district, transported the metals outward and redeposited them, enriching early veins, especially in the intermediate Zn plus Cu areas. Metals zones in lodes of the Butte district are the result of an intensely focused, Cu-rich hydrothermal plume that variably reworked the center of significantly larger, 10 m.y. older, Ag-Au-polymetallic lodes.

Montana↗
USGS2019

Testing the potential role of brine reflux in the formation of sedimentary exhalative (Sedex) ore deposits

Sedimentary exhalative (sedex) ore deposits are the world’s largest Zn-Pb deposits. While the geologic processes that formed these deposits are generally well understood, the fundamental hydrologic processes that drove these massive hydrothermal systems remain an area of debate. We use numerical modeling to test an emerging hypothesis, supported by recent ore genesis research and sedex basin analysis, that brine reflux flow systems produced and drove the fluids that formed sedex deposits. A previous numerical model of brine reflux, developed to study dolomitization, is adapted to a sedimentary basin with geologic features essential for sedex formation. We simulate the flow of evaporated brines through the basin and the evolution of salinity, temperature, and flow rates, and find that modeled values for these parameters for brines discharging to the seafloor exceed previously established physiochemical thresholds for ore formation (>170 g/L, >80°C, and total discharge volumes >107 m3 per meter perpendicular to the 2D model section). Sensitivity testing of this modest-sized basin highlights the large effect that aspects of the hydrogeologic framework can have on mineralizing potential of the reflux brines. Finally, modeling alternating periods of active and inactive evaporation produces pulsed brine reflux systems capable of producing multiple deposits of different age as observed in many sedex basins. The modeling thus supports the hypothesis that seawater evaporation on the basin margin significantly inboard of sedex deposits may be responsible for their formation. Sensitivity testing suggests that numerical models with more detailed, basin-specific geologic frameworks might be useful for assessing the mineral potential of sedimentary basins.

Ore Geology Reviews↗
USGS2018

Timing and genesis of ore formation in the Qarachilar Cu-Mo-Au deposit, Ahar-Arasbaran metallogenic zone, NW Iran: Evidence from geology, fluid inclusions, O–S isotopes and Re–Os geochronology

In the Qarachilar Cu-Mo-Au deposit of the Ahar–Arasbaran metallogenic zone (AAMZ), northwest Iran, mineralization occurs as three quartz-sulfide veins that cut granodiorite-quartz monzodiorite rocks of the Qaradagh batholith (QDB). Ore formation can be divided into three stages, with chalcopyrite, molybdenite, and gold-bearing pyrite appearing mainly in the first two stages. The main wall-rock alteration is silicification, and intermediate argillic, carbonate, and propylitic alteration. Fluid inclusion microthermometry indicates trapping of medium- to high-salinity (9.2–55 wt% NaCl equiv.) fluids at Qarachilar. Fluid inclusion trapping conditions are estimated to be 190 °C–530 °C and 0.1–3 kbar. The variable phase ratios as well as spatial coexisting of liquid- and vapor-rich two-phase and halite-bearing multiphase fluid inclusions homogenizing over the same temperatures are consistent with fluid boiling during ore formation. Obtained δ 18 O H2O values of quartz from ore-stage veins are +5.7‰ to +9.7‰, signifying that the ore–fluid system was predominantly magmatic water. The average calculated δ 34 S H2S values are 1 ± 1‰ for pyrite, chalcopyrite and molybdenite, consistent with a magmatic source for sulfur. Combined, the fluid inclusion and stable isotope data indicate that the ore-forming fluids at Qarachilar were magmatic in origin and were subsequently cooled and diluted by meteoric water. Fluid boiling and mixing facilitated hydrothermal alteration and mineralization. Molybdenite Re–Os dating shows that mineralization occurred at 42.35 ± 0.16 Ma, coincident with formation of porphyry Cu-Mo mineralization at Agarak deposit, and Hanqasar, Aygedzor and Dastakert prospects in the Lesser Caucasus. However, Qarachilar is older than all porphyry Cu-Mo mineralization in the AAMZ and Urumieh-Dokhtar magmatic arc (UDMA), which suggests that collision between Arabia and Eurasia were oblique and thus diachronous. Our data suggest that mineralization at Qarachilar is related to collisional Eocene magmatic–hydrothermal activity related to Neo-Tethys subduction, and shares a number of similarities with the vein-type Cu-Mo-Au mineralization related to Cu-Mo porphyries.

Ore Geology Reviews↗