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Poul Emsbo

Publications and source records attributed to Poul Emsbo.

36 records · Page 2Linked to original sources

Sedimentary exhalative (sedex) zinc-lead-silver deposit model

This report draws on previous syntheses and basic research studies of sedimentary exhalative (sedex) deposits to arrive at the defining criteria, both descriptive and genetic, for sedex-type deposits. Studies of the tectonic, sedimentary, and fluid evolution of modern and ancient sedimentary basins have also been used to select defining criteria. The focus here is on the geologic characteristics of sedex deposit-hosting basins that contain greater than 10 million metric tons of zinc and lead. The enormous size of sedex deposits strongly suggests that basin-scale geologic processes are involved in their formation. It follows that mass balance constraints of basinal processes can provide a conceptual underpinning for the evaluation of potential ore-forming mechanisms and the identification of geologic indicators for ore potential in specific sedimentary basins. Empirical data and a genetic understanding of the physicochemical, geologic, and mass balance conditions required for each of these elements are used to establish a hierarchy of quantifiable geologic criteria that can be used in U.S. Geological Survey national assessments. In addition, this report also provides a comprehensive evaluation of environmental considerations associated with the mining of sedex deposits.

Scientific Investigations Report↗

Sulfate and sulfide sulfur isotopes (δ34S and δ33S) measured by solution and laser ablation MC-ICP-MS: An enhanced approach using external correction

Isotope ratio measurements using a multi-collector inductively coupled plasma mass spectrometer (MC-ICP-MS) commonly use standard-sample bracketing with a single isotope standard for mass bias correction for elements with narrow-range isotope systems measured by MC-ICP-MS, e.g. Cu, Fe, Zn, and Hg. However, sulfur (S) isotopic composition (δ 34 S) in nature can range from at least − 40 to + 40‰, potentially exceeding the ability of standard-sample bracketing using a single sulfur isotope standard to accurately correct for mass bias. Isotopic fractionation via solution and laser ablation introduction was determined during sulfate sulfur (S sulfate ) isotope measurements. An external isotope calibration curve was constructed using in-house and National Institute of Standards and Technology (NIST) S sulfate isotope reference materials (RM) in an attempt to correct for the difference. The ability of external isotope correction for S sulfate isotope measurements was evaluated by analyzing NIST and United States Geological Survey (USGS) S sulfate isotope reference materials as unknowns. Differences in δ 34 S sulfate between standard-sample bracketing and standard-sample bracketing with external isotope correction for sulfate samples ranged from 0.72‰ to 2.35‰ over a δ 34 S range of 1.40‰ to 21.17‰. No isotopic differences were observed when analyzing S sulfide reference materials over a δ 34 S sulfide range of − 32.1‰ to 17.3‰ and a δ 33 S range of − 16.5‰ to 8.9‰ via laser ablation (LA)-MC-ICP-MS. Here, we identify a possible plasma induced fractionation for S sulfate and describe a new method using external isotope calibration corrections using solution and LA-MC-ICP-MS.

Chemical Geology↗

Rare earth elements in sedimentary phosphate deposits: Solution to the global REE crisis?

The critical role of rare earth elements (REEs), particularly heavy REEs (HREEs), in high-tech industries has created a surge in demand that is quickly outstripping known global supply and has triggered a worldwide scramble to discover new sources. The chemical analysis of 23 sedimentary phosphate deposits (phosphorites) in the United States demonstrates that they are significantly enriched in REEs. Leaching experiments using dilute H 2 SO 4 and HCl, extracted nearly 100% of their total REE content and show that the extraction of REEs from phosphorites is not subject to the many technological and environmental challenges that vex the exploitation of many identified REE deposits. Our data suggest that phosphate rock currently mined in the United States has the potential to produce a significant proportion of the world's REE demand as a byproduct. Importantly, the size and concentration of HREEs in some unmined phosphorites dwarf the world's richest REE deposits. Secular variation in phosphate REE contents identifies geologic time periods favorable for the formation of currently unrecognized high-REE phosphates. The extraordinary endowment, combined with the ease of REE extraction, indicates that such phosphorites might be considered as a primary source of REEs with the potential to resolve the global REE (particularly for HREE) supply shortage.

Gondwana Research↗

Precise determination of δ 88 Sr in rocks, minerals, and waters by double-spike TIMS: A powerful tool in the study of chemical, geologic, hydrologic and biologic processes

We present strontium isotopic ( 88 Sr/ 86 Sr and 87 Sr/ 86 Sr) results obtained by 87 Sr– 84 Sr double spike thermal ionization mass-spectrometry (DS-TIMS) for several standards as well as natural water samples and mineral samples of abiogenic and biogenic origin. The detailed data reduction algorithm and a user-friendly Sr-specific stand-alone computer program used for the spike calibration and the data reduction are also presented. Accuracy and precision of our δ 88 Sr measurements, calculated as permil (‰) deviations from the NIST SRM-987 standard, were evaluated by analyzing the NASS-6 seawater standard, which yielded δ 88 Sr = 0.378 ± 0.009‰. The first DS-TIMS data for the NIST SRM-607 potassium feldspar standard and for several US Geological Survey carbonate, phosphate, and silicate standards (EN-1, MAPS-4, MAPS-5, G-3, BCR-2, and BHVO-2) are also reported. Data obtained during this work for Sr-bearing solids and natural waters show a range of δ 88 Sr values of about 2.4‰, the widest observed so far in terrestrial materials. This range is easily resolvable analytically because the demonstrated external error (±SD, standard deviation) for measured δ 88 Sr values is typically ≤0.02‰. It is shown that the “true” 87 Sr/ 86 Sr value obtained by the DS-TIMS or any other external normalization method combines radiogenic and mass-dependent mass-fractionation effects, which cannot be separated. Therefore, the “true” 87 Sr/ 86 Sr and the δ 87 Sr parameter derived from it are not useful isotope tracers. Data presented in this paper for a wide range of naturally occurring sample types demonstrate the potential of the δ 88 Sr isotope tracer in combination with the traditional radiogenic 87 Sr/ 86 Sr tracer for studying a variety of biological, hydrological, and geological processes.

Journal of Analytical Atomic Spectrometry↗

In situ quantification of Br and Cl in minerals and fluid inclusions by LA-ICP-MS: a powerful tool to identify fluid sources

Bromine and chlorine are important halogens for fluid source identification in the Earth's crust, but until recently we lacked routine analytical techniques to determine the concentration of these elements in situ on a micrometer scale in minerals and fluid inclusions. In this study, we evaluate the potential of in situ Cl and Br measurements by LA-ICP-MS through analysis of a range of scapolite grains with known Cl and Br concentrations. We assess the effects of varying spot sizes, variable plasma energy and resolve the contribution of polyatomic interferences on Br measurements. Using well-characterised natural scapolite standards, we show that LA-ICP-MS analysis allows measurement of Br and Cl concentrations in scapolite, and fluid inclusions as small as 16 μm in diameter and potentially in sodalite and a variety of other minerals, such as apatite, biotite, and amphibole. As a demonstration of the accuracy and potential of Cl and Br analyses by LA-ICP-MS, we analysed natural fluid inclusions hosted in sphalerite and compared them to crush and leach ion chromatography Cl/Br analyses. Limit of detection for Br is ~8 μg g −1 , whereas relatively high Cl concentrations (> 500 μg g −1 ) are required for quantification by LA-ICP-MS. In general, our LA-ICP-MS fluid inclusion results agree well with ion chromatography (IC) data. Additionally, combined cathodoluminescence and LA-ICP-MS analyses on natural scapolites within a well-studied regional metamorphic suite in South Australia demonstrate that Cl and Br can be quantified with a ~25 μm resolution in natural minerals. This technique can be applied to resolve a range of hydrothermal geology problems, including determining the origins of ore forming brines and ore deposition processes, mapping metamorphic and hydrothermal fluid provinces and pathways, and constraining the effects of fluid–rock reactions and fluid mixing.

Chemical Geology↗

Genesis of the Touissit-Bou Beker Mississippi Valley-type district (Morocco-Algeria) and its relation to the Africa-Europe collision

The Mississippi Valley-type deposits of the Touissit-Bou Beker district are hosted by a 25 m thick sequence of diagenetically and hydrothermally dolomitized carbonate platform rocks of Aalenian-Bajocian age. The sulfide mineralization consists principally of galena and sphalerite and occurs as open-space fillings of voids and moderate to massive replacement of the medium- to coarse-grained host dolostone. Five types of dolomite have been distinguished, two of which (D 1 and D 2 ) are of replacement origin, whereas HD 1 , HD 2 , HD 3 occurring as open-space filling are of hydrothermal affiliation. Main ore controls include stratigraphy and lithology, carbonate dissolution, paleogeography, faults or faulted rocks, and availability of organic matter. Fluid inclusion data, along with Na-Cl-Br leachate, indicate that the ore-forming fluids correspond to evolved NaCl-CaCl 2 -KCl-MgCl 2 basin-derived hot (100° ± 20°C) saline brines (>20 wt % NaCl equiv) that acquired their high salinities and Ca/Na ratios through evaporation of seawater, and subsequent dolomitization and fluid-rock interactions. Stable isotope data for replacement and hydrothermal dolomites are tightly clustered and overlapping, with δ 18 O and δ 13 C values from 20.5 to 21.2 and 0.2 to 0.7‰, respectively. Similarly, sulfides yield δ 34 S values between 11.2 and 1.9‰, whereas those corresponding to the nearby Triassic gypsum cluster yield around 14‰. Altogether, these isotopic compositions are consistent with a basinal-type fluid with reduced sulfur very likely being derived through thermochemical reduction of dissolved sulfate, resulting in metal precipitation, and carbon of mainly marine Aalenian-Bajocian carbonate origin with a minor biogenic component. 87 Sr/ 86 Sr values of replacement dolostone are similar to those of ore-related hydrothermal dolomites, ranging from 0.70746 to 0.70833 and from 0.70769 to 0.70828, respectively, and are different from those of the Visean rhyodacite (0.71849–0.72167). Lead isotope ratios ( 206 Pb/ 204 Pb = 18.319–18.390; 207 Pb/ 204 Pb = 15.620–15.680; 208 Pb/ 204 Pb = 38.452–38.650) of sulfides are consistent with Pb being derived from the Visean rhyodacite and associated volcaniclastic rocks. The intimate link between faults and mineralization suggests the strong possibility of brine flow along both ENE-trending regional-scale faults and NW-SW-trending local-scale faults. The data suggest that MVT mineralization was emplaced during the late Neogene-Quaternary (i.e., ca. 15–0 Ma), possibly as a result of subsurface gravity-driven fluid flow in response to the collision between the African and Eurasian plates.

Touissit-bou Beker District↗

Testing the limits of Paleozoic chronostratigraphic correlation via high-resolution (<500 k.y.) integrated conodont, graptolite, and carbon isotope (δ 13 C carb ) biochemostratigraphy across the Llandovery–Wenlock (Silurian) boundary: Is a unified Phanerozoic time scale achievable?

The resolution and fidelity of global chronostratigraphic correlation are direct functions of the time period under consideration. By virtue of deep-ocean cores and astrochronology, the Cenozoic and Mesozoic time scales carry error bars of a few thousand years (k.y.) to a few hundred k.y. In contrast, most of the Paleozoic time scale carries error bars of plus or minus a few million years (m.y.), and chronostratigraphic control better than ??1 m.y. is considered "high resolution." The general lack of Paleozoic abyssal sediments and paucity of orbitally tuned Paleozoic data series combined with the relative incompleteness of the Paleozoic stratigraphic record have proven historically to be such an obstacle to intercontinental chronostratigraphic correlation that resolving the Paleozoic time scale to the level achieved during the Mesozoic and Cenozoic was viewed as impractical, impossible, or both. Here, we utilize integrated graptolite, conodont, and carbonate carbon isotope (??13Ccarb) data from three paleocontinents (Baltica, Avalonia, and Laurentia) to demonstrate chronostratigraphic control for upper Llando very through middle Wenlock (Telychian-Sheinwoodian, ~436-426 Ma) strata with a resolution of a few hundred k.y. The interval surrounding the base of the Wenlock Series can now be correlated globally with precision approaching 100 k.y., but some intervals (e.g., uppermost Telychian and upper Shein-woodian) are either yet to be studied in sufficient detail or do not show sufficient biologic speciation and/or extinction or carbon isotopic features to delineate such small time slices. Although producing such resolution during the Paleozoic presents an array of challenges unique to the era, we have begun to demonstrate that erecting a Paleozoic time scale comparable to that of younger eras is achievable. ?? 2010 Geological Society of America.

Geological Society of America Bulletin↗

Evolution of Ore Deposits and Technology Transfer Project: Isotope and Chemical Methods in Support of the U.S. Geological Survey Science Strategy, 2003-2008

Principal functions of the U.S. Geological Survey (USGS) Mineral Resources Program are providing assessments of the location, quantity, and quality of undiscovered mineral deposits, and predicting the environmental impacts of exploration and mine development. The mineral and environmental assessments of domestic deposits are used by planners and decisionmakers to improve the stewardship of public lands and public resources. Assessments of undiscovered mineral deposits on a global scale reveal the potential availability of minerals to the United States and other countries that manufacture goods imported to the United States. These resources are of fundamental relevance to national and international economic and security policy in our globalized world economy. Performing mineral and environmental assessments requires that predictions be made of the likelihood of undiscovered deposits. The predictions are based on geologic and geoenvironmental models that are constructed for the diverse types of mineral deposits from detailed descriptions of actual deposits and detailed understanding of the processes that formed them. Over the past three decades the understanding of ore-forming processes has benefited greatly from the integration of laboratory-based geochemical tools with field observations and other data sources. Under the aegis of the Evolution of Ore Deposits and Technology Transfer Project (referred to hereinafter as the Project), a 5-year effort that terminated in 2008, the Mineral Resources Program provided state-of-the-art analytical capabilities to support applications of several related geochemical tools to ore-deposit-related studies. The analytical capabilities and scientific approaches developed within the Project have wide applicability within Earth-system science. For this reason the Project Laboratories represent a valuable catalyst for interdisciplinary collaborations of the type that should be formed in the coming years for the United States to meet its natural-resources and natural-science needs. This circular presents an overview of the Project. Descriptions of the Project laboratories are given first including descriptions of the types of chemical or isotopic analyses that are made and the utility of the measurements. This is followed by summaries of select measurements that were carried out by the Project scientists. The studies are grouped by science direction. Virtually all of them were collaborations with USGS colleagues or with scientists from other governmental agencies, academia, or the private sector.

Circular↗

Geologic Criteria for the Assessment of Sedimentary Exhalative (Sedex) Zn-Pb-Ag Deposits

Sedex deposits account for more than 50 percent of the world's zinc and lead reserves and furnish more than 25 percent of the world's production of these two metals. This report draws on previous syntheses as well as on topical studies of deposits in sedex basins to determine the characteristics and processes that produced sedex deposits. This analysis also uses studies of the tectonic, sedimentary, and fluid evolution of modern and ancient sedimentary basins and mass balance constraints to identify the hydrothermal processes that are required to produce sedex deposits. This report demonstrates how a genetic model can be translated into geologic criteria that can be used in the U.S. Geological Survey National Assessments for sedex zinc-lead-silver deposits to define permissive tracts, assess the relative prospectivity of permissive tracts, and map favorability within permissive tracts.

Open-File Report↗

Composition and source of salinity of ore-bearing fluids in Cu-Au systems of the Carajás Mineral Province, Brazil

The composition and Cl/Br &ndash; NaCl ratios of highly saline aqueous inclusions from large tonnage (> 100 t) IOCG deposits (Sossego, Alvo 118, and Igarap&eacute; Bahia) and a Paleoproterozoic intrusion-related Cu-Au-(Mo-W-Bi-Sn) deposit (Breves; < 50 Mt)) in the Caraj&aacute;s Mineral Province have been analysed by LA-ICP-MS and ion chromatography. In both Cu-Au systems, brine inclusions are Ca-dominated (5 to 10 times more than in porphyry Cu-Au fluids), and contain percent level concentrations of Na and K. IOCG inclusion fluids, however, contain higher Sr, Ba, Pb, and Zn concentrations, but significantly less Bi, than the intrusion-related Breves inclusion fluids. Cu is consistently below detection limits in brine inclusions from the IOCG and intrusion-related systems and Fe was not detected in the latter. Cl/Br and Na/Cl ratios of the IOCG inclusion fluids range from entirely evaporative brines (bittern fluids; e.g. Igarap&eacute; Bahia and Alvo 118) to values that indicate mixing with magma-derived brines. Cl/Br and Na/Cl ratios of the Breves inclusion fluids strongly suggest the involvement of magmatic brines, but that possibly also incorporated bittern fluids. Collectively, these data demonstrate that residual evaporative and magmatic brines were important components of the fluid regime involved in the formation of Cu-Au systems in the Caraj&aacute;s Mineral Province.

Carajás Mineral Province↗

The source of Witwatersrand gold: Evidence from uraninite chemistry

An in-situ LA-ICP-MS study of different generations of uraninite from the Mesoarchaean Witwatersrand gold palaeoplacer deposits revealed unusually high Au concentrations in rounded, detrital uraninite grains but no detectable Au in secondary, hydrothermally mobilised uraninite. A Au-enriched uraninite-bearing magmatic host is suggested as a significant source for detrital gold in the Witwatersrand sediments.

Conference Paper↗

Reply to discussion on “Tectonic controls of Mississippi Valley-type lead–zinc mineralization in orogenic forelands”

Bradley and Leach (2003) focused on the tectonics of a subset of Mississippi Valley-type (MVT) lead–zinc deposits. Age assignments followed those given in a review of MVT deposits worldwide (Leach et al. 2001)—a paper that provoked a discussion by Kesler and Carrigan (2002) and reply by Leach et al. (2002), similar to the present exchange. While the new discussion by Kesler et al. (2004) does address tectonic issues, it also continues the old debate about the pros and cons of Rb–Sr isotopic and paleomagnetic dating of MVT deposits. We address these dating techniques first.

Mineralium Deposita↗

Nature of hydrothermal fluids at the shale-hosted Red Dog Zn-Pb-Ag deposits, Brooks Range, Alaska

The Red Dog Zn-Pb-Ag district in the western Brooks Range, northern Alaska, contains numerous shale-hosted Zn-Pb sulfide and barite deposits in organic-rich siliceous mudstone and shale, chert, and carbonate rocks of the Carboniferous Kuna Formation. The giant Red Dog shale-hosted deposits consist of a cluster of four orebodies (Main, Qanaiyaq, Aqqaluk, and Paalaaq) that lie within distinct thrust panels that offset a single ore deposit during the Mesozoic Brookian orogeny. These Zn-Pb-Ag-barite orebodies contain one of the world's largest reserves and resources of zinc. Fluid inclusions in samples of vein sphalerite, which accounts for about 20 percent of the ore in the Main deposit, and quartz that composes the bulk of the extensive silicification in the ore deposit, were studied by microthermometry, Raman spectrometry, and ion chromatography. The study of fluid inclusions in the vein sphalerite was limited by the intense postore deformation of the ore deposits. However, four primary aqueous fluid inclusion assemblages in vein sphalerite yield temperatures of homogenization of 115&deg; to 120&deg;C, 123&deg; to 127&deg;C, 110&deg; to 120&deg;C and 175&deg; to 180&deg;C. More abundant final-melting temperatures indicate that the fluid inclusions in sphalerite have salinities of about 14 to 19 wt percent NaCl equiv. The fluid inclusion electrolyte data show that the ore fluid responsible for the vein sphalerite derived its salinity from the evaporation of seawater. Considering the salinity of the fluid inclusions together with the electrolyte data, it is possible that the evaporative brine was initially about 30 wt percent saline fluid and that it mixed with a more dilute fluid somewhere along its flow path. The temperature, salinity, and electrolyte composition of vein sphalerite in the Red Dog deposits are remarkably similar to those characteristics in sphalerite veins near the Century zinc deposit, Australia. Together, these data compose the majority of information on the temperature and composition of sphalerite in deposits of this type. On the basis of data describing fluid inclusions in sphalerite and the geologic setting of the ore deposits, a "reflux brine" model is suggested for the Red Dog deposits. In this model, brines were produced in evaporative environments in supratidal carbonate facies of the Lisburne Group less than 100 km from the Red Dog deposits. These reflux brines may have infiltrated the underlying rocks of Endicott Group or fractured metasedimentary basement rocks. In the absence of a local heat source at the Red Dog deposits, the temperature of the ore fluids (~100&deg; to <200&deg;C) requires that the fluids circulated at depths between ~ 2.4 and 7.4 km. In the Red Dog area, the metalliferous fluids ascended into the organic-rich rocks of the Kuna Formation, probably along zones of active extensional faults or breaches in the shale aquitards overlying the aquifers in the Endicott Group. Fluid inclusions were also studied in the abundant quartz that constitutes the majority of the silica rock in the ore deposits. This postore quartz extensively replaced barite and was traditionally thought to be part of the main ore event. Primary fluid inclusion assemblages contain two-phase aqueous inclusions, single-phase inclusions of dense methane, or both. Primary assemblages that contain single-phase, dense-methane inclusions together with two-phase aqueous inclusions yield consistent homogenization temperatures that provide unequivocal evidence for the coeval trapping of immiscible gas and aqueous fluids. The densities of the methane inclusions, together with the temperature of homogenization of coexisting aqueous fluid inclusions, show that these fluid inclusions were trapped between pressures of 800 and 3,400 bars and temperatures between 187&deg; and 214&deg;C. The pressures obtained provide unequivocal evidence that the quartz formed after ore deposition in the Carboniferous because such high fluid pressures could only have been produced from thrust loading during the Mesozoic Brookian orogeny. The observed large variation in pressure is best explained by transient fluid pressures from hydrostatic to lithostatic conditions during thrust loading. The 3,400 bars pressure corresponds with about 12 km of lithostatic burial, whereas the lower pressures (800 bars) correspond with about 8 km of hydrostatic pressure. Because of their low salinity (0-5 wt % NaCl equiv) the electrolyte compositions of the quartz fluid inclusions do not constrain their origin.

Alaska↗

Origin of high-grade gold ore, source of ore fluid components, and genesis of the Meikle and neighboring Carlin-type deposits, Northern Carlin Trend, Nevada

The Meikle mine exploits one of the world’s highest grade Carlin-type gold deposits with reserves of ca. 220 t gold at an average grade of 24.7 g/t. Locally, gold grades exceed 400 g/t. Several geologic events converged at Meikle to create these spectacular gold grades. Prior to mineralization, a Devonian hydrothermal system altered the Bootstrap limestone to Fe-rich dolomite. Subsequently the rocks were brecciated by faulting and Late Jurassic intrusive activity. The resulting permeability focused flow of late Eocene Carlin-type ore fluids and allowed them to react with the Fe-rich dolomite. Fluid inclusion data and mineral assemblages indicate that these fluids were hot (ca. 220°C),of moderate salinity (<6 wt % NaCl equiv), acidic, and H 2 S rich. Gold-rich pyrite formed by dissolution of dolomite and sulfidation of its contained Fe. Where dissolution and replacement were complete, ore-stage pyrite and other insoluble minerals were all that remained. Locally, these minerals accumulated as internal sediments in dissolution cavities to form ore with gold grades >400 g/t. Petrographic observations, geochemical data, and stable isotope results from the Meikle mine and other deposits at the Goldstrike mine place important constraints on genetic models for Meikle and other Carlin-type gold deposits on the northern Carlin trend. The ore fluids were meteoric water ( δ D = –135‰, δ 18 O = –5‰) that interacted with sedimentary rocks at a water/rock ratio of ca. 1 and temperatures of ca. 220°C. The absence of significant silicification suggests that there was little cooling of the ore fluids during mineralization. These two observations strongly suggest that ore fluids were not derived from deep sources but instead flowed parallel to isotherms. The gold was transported by H 2 S ( δ 34 S = 9‰), which was derived from Paleozoic sedimentary rocks. The presence of auriferous sedimentary exhalative mineralization in the local stratigraphic sequence raises the possibility that preexisting concentrations of gold contributed to the Carlin-type deposits. Taken together our observations suggest that meteoric water evolved to become an ore fluid by shallow circulation through previously gold- and sulfur-enriched rocks. Carlin-type gold deposits formed where these fluids encountered permeable, reactive Fe-rich rocks.

Nevada↗

Origin and significance of postore dissolution collapse breccias cemented with calcite and barite at the Meikle gold deposit, Northern Carlin trend, Nevada

The final event in a complicated hydrothermal history at the Meikle gold deposit was gold deficient but caused extensive postore dissolution of carbonate, collapse brecciation, and precipitation of calcite and barite crystals in the resulting cavities. Although previously interpreted to be part of the Carlin-type hydrothermal system, crosscutting relationships and U-Th-Pb geochronology constrain this hydrothermal event to late Pliocene time (ca. 2 Ma), nearly 36 Ma after ore formation. Mineralogic, fluid inclusion, and stable isotope data indicate that postore hydrothermal fluids were reduced, H 2 S-rich, unevolved meteoric waters ( δ 18 O = –17‰) of low temperature (ca. 65°C). The δ 18 O values of barite and calcite indicate that these minerals were in isotopic equilibrium, requiring that barite SO 4 was derived from the oxidation of reduced sulfur; however, preexisting sulfides in breccia cavities were not oxidized. The δ 34 S (15‰) values of barite are higher than those of local bulk sulfide and supergene alunite indicating that SO 4 was not derived from supergene oxidation of local sulfide minerals. The 15 per mil δ 34 S value suggests that the H 2 S in the fluids may have been leached from sulfur-rich organic matter in the local carbonaceous sedimentary rocks. A reduced H 2 S-rich fluid is also supported by the bright cathodoluminescence of calcite which indicates that it is Mn rich and Fe poor. Calcite has a narrow range of δ 13 C values (0.3–1.8‰) that are indistinguishable from those of the host Bootstrap limestone, indicating that CO 2 in the fluid was from dissolution of the local limestone. These data suggest that dissolution and brecciation of the Bootstrap limestone occurred where H 2 S-rich fluids encountered more oxidizing fluids and formed sulfuric acid (H 2 SO 4 ). Intense fracturing in the mine area by previous structural and hydrothermal events probably provided conduits for the descent of oxidized surface water which mixed with the underlying H 2 S-rich waters to form the dissolving acid. The surface-derived fluid apparently contained sufficient oxygen to produce H 2 SO 4 from H 2 S but not enough to alter pyrite to Fe oxide. Although H 2 S is an important gold-transporting ligand, the temperature was too low to transport a significant amount of gold. The presence of analogous calcite- and barite-lined cavities in other Carlin-type deposits suggests that the generation (and oxidation) of H 2 S-rich meteoric waters was a common phenomenon in north-central Nevada. Previous sulfur isotope studies have also shown that the Paleozoic sedimentary rocks were the principal source of H 2 S in Devonian sedimentary exhalative-type, Jurassic intrusion-related, Eocene Carlin-type, and Miocene low-sulfidation gold deposits in the region. The similar sulfur source in all of these systems suggests that basin brines, magmatic fluids, and meteoric waters all evolved to be H 2 S-rich ore fluids by circulation through Paleozoic sedimentary rocks. Thus, although not directly related to gold mineralization, the recent hydrologic history of the deposit provides important clues to earlier ore-forming processes that were responsible for gold mineralization.

Nevada↗