Geology topics

John F. Slack

Publications and source records attributed to John F. Slack.

At least 37 records · Page 2Linked to original sources

USGS2016

Geochemistry of host rocks in the Howards Pass district, Yukon-Northwest Territories, Canada: implications for sedimentary environments of Zn-Pb and phosphate mineralization

Detailed lithogeochemical data are reported here on early Paleozoic sedimentary rocks that host the large Howards Pass stratiform Zn-Pb deposits in Yukon-Northwest Territories. Redox-sensitive trace elements (Mo, Re, V, U) and Ce anomalies in members of the Duo Lake Formation record significant environmental changes. During the deposition of lower footwall units (Pyritic siliceous and Calcareous mudstone members), bottom waters were anoxic and sulphidic, respectively; these members formed in a marginal basin that may have become increasingly restricted with time. Relative to lower members, a major environmental change is proposed for deposition of the overlying Lower cherty mudstone member, which contains phosphorite beds up to ∼0.8 m thick in the upper part, near the base of the Zn-Pb deposits. The presence of these beds, together with models for modern phosphorite formation, suggests P input from an upwelling system and phosphorite deposition in an upper slope or outer shelf setting. The overlying Active mudstone member contains stratabound to stratiform Zn-Pb deposits within black mudstone and gray calcareous mudstone. Data for unmineralized black mudstone in this member indicate deposition under diverse redox conditions from suboxic to sulphidic. Especially distinctive in this member are uniformly low ratios of light to heavy rare earth elements that are unique within the Duo Lake Formation, attributed here to the dissolution of sedimentary apatite by downward-percolating acidic metalliferous brines. Strata that overlie the Active member (Upper siliceous mudstone member) consist mainly of black mudstone with thin (0.5–1.5 cm) laminae of fine-grained apatite, recording continued deposition on an upper slope or outer shelf under predominantly suboxic bottom waters. Results of this study suggest that exploration for similar stratiform sediment-hosted Zn-Pb deposits should include the outer parts of ancient continental margins, especially at and near stratigraphic transitions from marginal basin facies to overlying slope or shelf facies.

Mineralium Deposita↗

USGS2016

Re-Os systematics and age of pyrite associated with stratiform Zn-Pb mineralization in the Howards Pass district, Yukon and Northwest Territories, Canada

Stratiform Zn-Pb deposits hosted in unmetamorphosed carbonaceous and siliceous mudstones of the Ordovician to Silurian Duo Lake Formation define the Howards Pass district in Yukon Territory and Northwest Territories, western Canada. Collectively, the deposits are amongst the largest in the world, containing drill-indicated and inferred resources of 423 Mt at 4.84 % Zn and 1.59 % Pb. Sulphide textures include (a) fine-scale laminations of sphalerite, galena, and pyrite from <0.05 mm to 1 cm thick, interbedded with carbonaceous sedimentary rock; (b) layers of coarse sulphide that are structurally controlled by microfolds; and (c) veins that cut bedding and sulphide laminations. The finely interlaminated nature of sulphides with mudstone has been used as evidence for syngenetic mineralizing processes, whereas paleomagnetic data determined on coarse layered sulphides suggest a Middle Jurassic age of mineralization. Here, we present new rhenium-osmium (Re-Os) isotopic data for 12 pyrite separates obtained from 4 laminated sulphide-rich samples from the XY Central (XYC) and Don (DON) deposits and for 1 unmineralized organic-rich mudstone ∼20 m stratigraphically below the sulphide-bearing zone. Pyrite separates that lack mudstone inclusions (“pure”) from the XYC deposit contain 2.2 to 4.0 ppb Re and 93.4 to 123.4 ppt Os; pure pyrite from the DON deposit is significantly more enriched in Re and Os (34–37 ppb Re; 636.8–694.9 ppt Os). The 187 Re/ 188 Os values of pure pyrite separates from the XYC and DON deposits range from 137.6 to 197 and 182.1 to 201.4, respectively. Regression of all pure pyrite Re-Os data from both deposits yields an isochron age of 442 ± 14 Ma (MSWD = 7.4) and an initial 187 Os/ 188 Os (Os i ) value of 0.71 ± 0.07. The Re-Os age indicates that the early phase of pyrite precipitation (and by inference, sphalerite and galena) occurred during the early Silurian, consistent with biostratigraphic ages of the host rocks. The Os i value of ∼0.8 for earliest Silurian seawater recorded from organic-rich shale in the basal Silurian Global Stratotype Section and Point (GSSP) at Dobs Linn, Scotland is very similar to that provided by the Howards Pass pyrite regression and hence suggests a hydrogenous (seawater) source of Os for the pyrite. Therefore, two possible sources of Os are (1) the Zn- and Pb-bearing hydrothermal fluid that leached Os from footwall sedimentary rocks, which were deposited in seawater, or (2) directly from seawater during precipitation of the pyrite, which suggests that the Os content of the hydrothermal fluid was minor relative to that of seawater.

Northwest Territories, Yukon↗

USGS2015

Depositional conditions for the Kuna Formation, Red Dog Zn-PB-Ag-Barite District, Alaska, inferred from isotopic and chemical proxies

Water column redox conditions, degree of restriction of the depositional basin, and other paleoenvironmental parameters have been determined for the Mississippian Kuna Formation of northwestern Alaska from stratigraphic profiles of Mo, Fe/Al, and S isotopes in pyrite, C isotopes in organic matter, and N isotopes in bulk rock. This unit is important because it hosts the Red Dog and Anarraaq Zn-Pb-Ag ± barite deposits, which together constitute one of the largest zinc resources in the world. The isotopic and chemical proxies record a deep basin environment that became isolated from the open ocean, became increasingly reducing, and ultimately became euxinic. The basin was ventilated briefly and then became isolated again just prior to its demise as a discrete depocenter with the transition to the overlying Siksikpuk Formation. Ventilation corresponded approximately to the initiation of bedded barite deposition in the district, whereas the demise of the basin corresponded approximately to the formation of the massive sulfide deposits. The changes in basin circulation during deposition of the upper Kuna Formation may have had multiple immediate causes, but the underlying driver was probably extensional tectonic activity that also facilitated fluid flow beneath the basin floor. Although the formation of sediment-hosted sulfide deposits is generally favored by highly reducing conditions, the Zn-Pb deposits of the Red Dog district are not found in the major euxinic facies of the Kuna basin, nor did they form during the main period of euxinia. Rather, the deposits occur where strata were permeable to migrating fluids and where excess H 2 S was available beyond what was produced in situ by decomposition of local sedimentary organic matter. The known deposits formed mainly by replacement of calcareous strata that gained H 2 S from nearby highly carbonaceous beds (Anarraaq deposit) or by fracturing and vein formation in strata that produced excess H 2 S by reductive dissolution of preexisting barite (Red Dog deposits).

Alaska↗

USGS2015

Hydrothermal, biogenic, and seawater components in metalliferous black shales of the Brooks Range, Alaska: Synsedimentary metal enrichment in a carbonate ramp setting

Trace element and Os isotope data for Lisburne Group metalliferous black shales of Middle Mississippian (early Chesterian) age in the Brooks Range of northern Alaska suggest that metals were sourced chiefly from local seawater (including biogenic detritus) but also from externally derived hydrothermal fluids. These black shales are interbedded with phosphorites and limestones in sequences 3 to 35 m thick; deposition occurred mainly on a carbonate ramp during intermittent upwelling under varying redox conditions, from suboxic to anoxic to sulfidic. Deposition of the black shales at ~335 Ma was broadly contemporaneous with sulfide mineralization in the Red Dog and Drenchwater Zn-Pb-Ag deposits, which formed in a distal marginal basin. Relative to the composition of average black shale, the metalliferous black shales ( n = 29) display large average enrichment factors (>10) for Zn (10.1), Cd (11.0), and Ag (20.1). Small enrichments (>2–<10) are shown by V, Cr, Ni, Cu, Mo, Pd, Pt, U, Se, Y, and all rare earth elements except Ce, Nd, and Sm. A detailed stratigraphic profile over 23 m in the Skimo Creek area (central Brooks Range) indicates that samples from at and near the top of the section, which accumulated during a period of major upwelling and is broadly correlative with the stratigraphic levels of the Red Dog and Drenchwater Zn-Pb-Ag deposits, have the highest Zn/TOC (total organic carbon), Cu/TOC, and Tl/TOC ratios for calculated marine fractions (no detrital component) of these three metals. Average authigenic (detrital-free) contents of Mo, V, U, Ni, Cu, Cd, Pb, Ge, Re, Se, As, Sb, Tl, Pd, and Au show enrichment factors of 4.3 × 10 3 to 1.2 × 10 6 relative to modern seawater. Such moderate enrichments, which are common in other metalliferous black shales, suggest wholly marine sources (seawater and biogenic material) for these metals, given similar trends for enrichment factors in organic-rich sediments of modern upwelling zones on the Namibian, Peruvian, and Chilean shelves. The largest enrichment factors for Zn and Ag are much higher (1.4 × 10 7 and 2.9 × 10 7 , respectively), consistent with an appreciable hydrothermal component. Other metals such as Cu, Pb, and Tl that are concentrated in several black shale samples, and are locally abundant in the Red Dog and Drenchwater Zn-Pb-Ag deposits, may have a partly hydrothermal origin but this cannot be fully established with the available data. Enrichments in Cr (up to 7.8 × 10 6 ) are attributed to marine and not hydrothermal processes. The presence in some samples of large enrichments in Eu (up to 6.1 × 10 7 ) relative to modern seawater and of small positive Eu anomalies (Eu/Eu* up to 1.12) are considered unrelated to hydrothermal activity, instead being linked to early diagenetic processes within sulfidic pore fluids. Initial Os isotope ratios ( 187 Os/ 188 Os) calculated for a paleontologically based depositional age of 335 Ma reveal moderately unradiogenic values of 0.24 to 0.88 for four samples of metalliferous black shale. A proxy for the ratio of coeval early Chesterian seawater is provided by initial ( 187 Os/ 188 Os) 335 Ma ratios of four unaltered black shales of the coeval Kuna Formation that average 1.08, nearly identical to the initial ratio of 1.06 for modern seawater. Evaluation of possible sources of unradiogenic Os in the metalliferous black shales suggests that the most likely source was mafic igneous rocks that were leached by externally derived hydrothermal fluids. This unradiogenic Os is interpreted to have been leached by deeply circulating hydrothermal fluids in the Kuna basin, followed by venting of the fluids into overlying seawater. We propose that metal-bearing hydrothermal fluids that formed Zn-Pb-Ag deposits such as Red Dog or Drenchwater vented into seawater in a marginal basin, were carried by upwelling currents onto the margins of a shallow-water carbonate platform, and were then deposited in organic-rich muds, together with seawater- and biogenically derived components, by syngenetic sedimentary processes. Metal concentration in the black shales was promoted by high biologic productivity, sorption onto organic matter, diffusion across redox boundaries, a low sedimentation rate, and availability of H 2 S in bottom waters and pore fluids.

Alaska↗

USGS2015

Measurement of in situ sulfur isotopes by laser ablation multi-collector ICPMS: opening Pandora’s Box

Laser ablation multi-collector ICPMS is a modern tool for in situ measurement of S isotopes. Advantages of the technique are speed of analysis and relatively minor matrix effects combined with spatial resolution sufficient for many applications. The main disadvantage is a more destructive sampling mechanism relative to the ion microprobe technique. Recent advances in instrumentation allow precise measurement with spatial resolutions down to 25 microns. We describe specific examples from economic geology where increased spatial resolution has greatly expanded insights into the sources and evolution of fluids that cause mineralization and illuminated genetic relations between individual deposits in single mineral districts.

Procedia Earth and Planetary Science↗

USGS2015

Oxic to anoxic transition in bottom waters during formation of the Citronen Fjord sediment-hosted Zn-Pb deposit, North Greenland

Bulk geochemical data acquired for host sedimentary rocks to the Late Ordovician Citronen Fjord sediment-hosted Zn-Pb deposit in North Greenland constrain the redox state of bottom waters prior to and during sulphide mineralization. Downhole profiles for one drill core show trends for redox proxies (MnO, Mo, Ce anomalies) that suggest the local basin bottom waters were initially oxic, changing to anoxic and locally sulphidic concurrent with sulphide mineralization. We propose that this major redox change was caused by two broadly coeval processes (1) emplacement of debris-flow conglomerates that sealed off the basin from oxic seawater, and (2) venting of reduced hydrothermal fluids into the basin. Both processes may have increased H2S in bottom waters and thus prevented the oxidation of sulphides on the sea floor.

Conference Paper↗

USGS2014

The Late Cretaceous Middle Fork caldera, its resurgent intrusion, and enduring landscape stability in east-central Alaska

Dissected caldera structures expose thick intracaldera tuff and, uncommonly, cogenetic shallow plutons, while remnants of correlative outflow tuffs deposited on the pre-eruption ground surface record elements of ancient landscapes. The Middle Fork caldera encompasses a 10 km × 20 km area of rhyolite welded tuff and granite porphyry in east-central Alaska, &sim;100 km west of the Yukon border. Intracaldera tuff is at least 850 m thick. The K-feldspar megacrystic granite porphyry is exposed over much of a 7 km × 12 km area having 650 m of relief within the western part of the caldera fill. Sensitive high-resolution ion microprobe with reverse geometry (SHRIMP-RG) analyses of zircon from intracaldera tuff, granite porphyry, and outflow tuff yield U-Pb ages of 70.0 ± 1.2, 69.7 ± 1.2, and 71.1 ± 0.5 Ma (95% confidence), respectively. An aeromagnetic survey indicates that the tuff is reversely magnetized, and, therefore, that the caldera-forming eruption occurred in the C31r geomagnetic polarity chron. The tuff and porphyry have arc geochemical signatures and a limited range in SiO 2 of 69 to 72 wt%. Although their phenocrysts differ in size and abundance, similar quartz + K-feldspar + plagioclase + biotite mineralogy, whole-rock geochemistry, and analytically indistinguishable ages indicate that the tuff and porphyry were comagmatic. Resorption of phenocrysts in tuff and porphyry suggests that these magmas formed by thermal rejuvenation of near-solidus or solidified crystal mush. A rare magmatic enclave (54% SiO 2 , arc geochemical signature) in the porphyry may be similar to parental magma and provides evidence of mafic magma and thermal input. The Middle Fork is a relatively well preserved caldera within a broad region of Paleozoic metamorphic rocks and Mesozoic plutons bounded by northeast-trending faults. In the relatively downdropped and less deeply exhumed crustal blocks, Cretaceous–Early Tertiary silicic volcanic rocks attest to long-term stability of the landscape. Within the Middle Fork caldera, the granite porphyry is interpreted to have been exposed by erosion of thick intracaldera tuff from an asymmetric resurgent dome. The Middle Fork of the North Fork of the Fortymile River incised an arcuate valley into and around the caldera fill on the west and north and may have cut down from within an original caldera moat. The 70 Ma land surface is preserved beneath proximal outflow tuff at the west margin of the caldera structure and beneath welded outflow tuff 16–23 km east-southeast of the caldera in a paleovalley. Within &sim;50 km of the Middle Fork caldera are 14 examples of Late Cretaceous (?)–Tertiary felsic volcanic and hypabyssal intrusive rocks that range in area from <1 km 2 to &sim;100 km 2 . Rhyolite dome clusters north and northwest of the caldera occupy tectonic basins associated with northeast-trending faults and are relatively little eroded. Lava of a latite complex, 12–19 km northeast of the caldera, apparently flowed into the paleovalley of the Middle Fork of the North Fork of the Fortymile River. To the northwest of the Middle Fork caldera, in the Mount Harper crustal block, mid-Cretaceous plutonic rocks are widely exposed, indicating greater total exhumation. To the southeast of the Middle Fork block, the Mount Veta block has been uplifted sufficiently to expose a ca. 68–66 Ma equigranular granitic pluton. Farther to the southeast, in the Kechumstuk block, the flat-lying outflow tuff remnant in Gold Creek and a regionally extensive high terrace indicate that the landscape there has been little modified since 70 Ma other than entrenchment of tributaries in response to post–2.7 Ma lowering of base level of the Yukon River associated with advance of the Cordilleran ice sheet.

Alaska↗

USGS2014

Carbonate margin, slope, and basin facies of the Lisburne Group (Carboniferous-Permian) in northern Alaska

The Lisburne Group (Carboniferous-Permian) consists of a carbonate platform that extends for >1000 km across northern Alaska, and diverse margin, slope, and basin facies that contain world-class deposits of Zn and Ba, notable phosphorites, and petroleum source rocks. Lithologic, paleontologic, isotopic, geochemical, and seismic data gathered from outcrop and subsurface studies during the past 20 years allow us to delineate the distribution, composition, and age of the off-platform facies, and to better understand the physical and chemical conditions under which they formed. The southern edge of the Lisburne platform changed from a gently sloping, homoclinal ramp in the east to a tectonically complex, distally steepened margin in the west that was partly bisected by the extensional Kuna Basin (~200 by 600 km). Carbonate turbidites, black mudrocks, and radiolarian chert accumulated in this basin; turbidites were generated mainly during times of eustatic rise in the late Early and middle Late Mississippian. Interbedded black mudrocks (up to 20 wt% total organic carbon), granular and nodular phosphorite (up to 37 wt% P 2 O 5 ), and fine-grained limestone rich in radiolarians and sponge spicules formed along basin margins during the middle Late Mississippian in response to a nutrient-rich, upwelling regime. Detrital zircons from a turbidite sample in the western Kuna Basin have mainly Neoproterozoic through early Paleozoic U-Pb ages (~900-400 Ma), with subordinate populations of Mesoproterozoic and late Paleoproterozoic grains. This age distribution is similar to that found in slightly older rocks along the northern and western margins of the basin. It also resembles age distributions reported from Carboniferous and older strata elsewhere in northwestern Alaska and on Wrangel Island. Geochemical and isotopic data indicate that suboxic, denitrifying conditions prevailed in the Kuna Basin and along its margins. High V/Mo, Cr/Mo, and Re/Mo ratios (all marine fractions [MF]) and low MnO contents (<0.01 wt%) characterize Lisburne black mudrocks. Low Qmf/Vmf ratios (mostly 0.8-4.0) suggest moderately to strongly denitrifying conditions in suboxic bottom waters during siliciclastic and phosphorite sedimentation. Elevated to high Mo contents (31-135 ppm) in some samples are consistent with seasonal to intermittent sulfidic conditions in bottom waters, developed mainly along the basin margin. High d 15 N values (6-120) imply that the waters supplying nutrients to primary producers in the photic zone had a history of denitrification either in the water column or in underlying sediments. Demise of the Lisburne platform was diachronous and reflects tectonic, eustatic, and environmental drivers. Southwestern, south-central, and northwestern parts of the platform drowned during the Late Mississippian, coincident with Zn and Ba metallogenesis within the Kuna Basin and phosphogenesis along basin margins. This drowning was temporary (except in the southwest) and likely due to eutrophication associated with upwelling and sea-level rise enhanced by regional extension, which allowed suboxic, denitrifying waters to form on platform margins. Final drowning in the southcentral area occurred in the Early Pennsylvanian and also may have been linked to regional extension. In the northwest, platform sedimentation persisted into the Permian; its demise there appears to have been due to increased siliciclastic input. Climatic cooling may have produced additional stress on parts of the Lisburne platform biota during Pennsylvanian and Permian times.

Alaska↗

USGS2014

Reconstruction of an early Paleozoic continental margin based on the nature of protoliths in the Nome Complex, Seward Peninsula, Alaska

The Nome Complex is a large metamorphic unit that sits along the southern boundary of the Arctic Alaska–Chukotka terrane, the largest of several micro continental fragments of uncertain origin located between the Siberian and Laurentian cratons. The Arctic Alaska–Chukotka terrane moved into its present position during the Mesozoic; its Mesozoic and older movements are central to reconstruction of Arctic tectonic history. Accurate representation of the Arctic Alaska–Chukotka terrane in reconstructions of Late Proterozoic and early Paleozoic paleogeography is hampered by the paucity of information available. Most of the Late Proterozoic to Paleozoic rocks in the Alaska–Chukotka terrane were penetratively deformed and recrystallized during the Mesozoic deformational events; primary features and relationships have been obliterated, and age control is sparse. We use a variety of geochemical, geochronologic, paleontologic, and geologic tools to read through penetrative deformation and reconstruct the protolith sequence of part of the Arctic Alaska–Chukotka terrane, the Nome Complex. We confirm that the protoliths of the Nome Complex were part of the same Late Proterozoic to Devonian continental margin as weakly deformed rocks in the southern and central part of the terrane, the Brooks Range. We show that the protoliths of the Nome Complex represent a carbonate platform (and related rocks) that underwent incipient rifting, probably during the Ordovician, and that the carbonate platform was overrun by an influx of siliciclastic detritus during the Devonian. During early phases of the transition to siliciclastic deposition, restricted basins formed that were the site of sedimentary exhalative base-metal sulfide deposition. Finally, we propose that most of the basement on which the largely Paleozoic sedimentary protolith was deposited was subducted during the Mesozoic.

Alaska↗

USGS2014

Late Devonian–Mississippian(?) Zn-Pb(-Ag-Au-Ba-F) deposits and related aluminous alteration zones in the Nome Complex, Seward Peninsula, Alaska

Stratabound base-metal sulfide deposits and occurrences are present in metasedimentary rocks of the Neoproterozoic and Paleozoic Nome Complex on south-central Seward Peninsula, Alaska. Stratabound and locally stratiform deposits including Aurora Creek (Zn-Au-Ba-F), Wheeler North (Pb-Zn-Ag-Au-F), and Nelson (Zn-Pb- Cu-Ag), consist of lenses typically 0.5–2.0 m thick containing disseminated to semimassive sulfides. Host strata of the Aurora Creek and Wheeler North deposits are variably calcareous and graphitic siliciclastic metasedimentary rocks of Middle Devonian or younger age based on detrital zircon geochronology; the Nelson deposit is within Ordovician–Devonian marble (Till et al., this volume, Chapter 4). Deformed veins such as Quarry (Zn-Pb-Ag-Ba-F) and Galena (Pb-Zn-Ag-F) occur in a unit composed mainly of marble and schist; fossil and detrital zircon data indicate that this unit contains rocks of Ordovician, Silurian, and Devonian age. None of these Zn- and Pbrich deposits or occurrences has spatially associated metavolcanic or intrusive rocks. All were deformed and metamorphosed to blueschist facies and then retrograded to greenschist facies during the Jurassic and Early Cretaceous Brookian orogeny. Disseminated Cu-rich deposits including Copper King (Cu-Bi-Sb-Pb-Ag-Au) and Wheeler South (Cu-Ag-Au) occur in silicified carbonate rocks and have textures that indicate a pre- to syn-metamorphic origin. The Zn- and Pb-rich sulfide deposits and occurrences consist mainly of pyrite, sphalerite, and/or galena in a gangue of quartz and carbonate. Minor minerals include arsenopyrite, chalcopyrite, magnetite, pyrrhotite, tetrahedrite, barite, fluorite, and chlorite; gold and electrum are trace to minor constituents locally. Sphalerite is uniformly unzoned and commonly aligned in the dominant foliation. These textures, together with the presence of folded layers of barite at Aurora Creek and folded sulfi de layers at Wheeler North, indicate that mineralization in the stratabound deposits predated deformation and metamorphism. Electron microprobe (EMP) analyses of the carbonate gangue show three major compositions comprising siderite, ankerite, and lesser dolomite. The Cu-rich deposits differ in containing chalcopyrite and bornite in a quartzose matrix. Altered wall rocks surrounding the Zn- and Pb-rich deposits and occurrences have aluminous assemblages composed of muscovite + chloritoid + siderite + chlorite + quartz ± tourmaline ± ilmenite ± apatite ± monazite. Muscovite within these assemblages and in sulfide-rich samples is phengitic and locally enriched in barium; chloritoid at Aurora Creek is enriched in zinc. Minor minerals including pyrite, sphalerite, galena, chalcopyrite, barite, and hyalophane occur as fine-grained disseminations. These altered rocks vary from small lenses a few meters thick to large zones tens of meters in thickness that extend along strike, discontinuously, for 4 km or more. Whole-rock geochemical analyses of the altered rocks from deposit-proximal and deposit-distal settings reveal generally lower SiO 2 /Al 2 O 3 ratios and higher Fe 2 O 3 T /MgO ratios compared to those of unaltered clastic metasedimentary rocks of the Nome Complex and of average shale or graywacke. The deposit-proximal samples are also characterized by anomalously high Zn, Pb, Hg, and Sb, relative to the unaltered metasediments. These data, together with mass change calculations, suggest that the aluminous rocks formed as replacements of permeable graywacke in semi-conformable alteration zones, beneath the seafloor contemporaneously with Zn-and/or Pb-rich sulfide mineralization. Exposures of all three stratabound Zn-Pb deposits show evidence of deformation and recrystallization that occurred in a largely brittle deformational regime. This evidence includes small faults and veins that cut foliation and localized zones of breccia. Sulfide minerals, fluorite, quartz, chlorite, and carbonate minerals crystallized within these structures, which probably formed during Cretaceous deformation of the Nome Complex. Previous studies of the Zn-Pb(-Ag-Au-Ba-F) deposits and occurrences have invoked models of epigenetic veins, volcanogenic massive sulfides (VMS), or carbonate- replacement deposits (CRD). In contrast, our field and laboratory data (including sulfur isotopes; Shanks et al., this volume) suggest that these Zn- and/or Pb-rich deposits represent different levels of sediment-hosted, seafloor-hydrothermal systems, with stratabound and locally stratiform deposits such as Aurora Creek and Wheeler North having formed on the seafloor and/or in the shallow subsurface like many sedimentary-exhalative (SEDEX) deposits worldwide. The deformed veins such as Quarry and Galena are interpreted to have formed deep in the subsurface, possibly as feeders to overlying SEDEX deposits such as Aurora Creek. Formation of all of the Zn- and Pb-rich deposits and occurrences took place during episodic rifting of the continental margin between the Ordovician and Mississippian(?). Regional relationships are consistent with at least some of the deposits having formed in Late Devonian–Mississippian(?) time.

Alaska↗

USGS2014

Pb isotope geochemistry of stratabound Zn-Pb(-Ag-Au-Ba-F) deposits and occurrences in the Nome Complex, Seward Peninsula, Alaska: Metal sources and regional comparisons

A detailed study of the Pb isotope geochemistry of Zn-Pb(-Ag-Au-Ba-F) stratabound sulfide deposits within metasedimentary rocks of the Neoproterozoic to Mississippian(?) Nome Complex provides key information for understanding deposit genesis and crustal evolution. A total of 106 new analyses of galena (and other sulfi des) and metasedimentary rocks hosting the deposits shows that (1) Pb isotope signatures of the deposits are heterogeneous when considered as a group; (2) the stratabound Nelson deposit, and deformed veins at Quarry and Galena, are isotopically similar; (3) stratabound and locally stratiform lenses such as Wheeler North and Aurora Creek had different isotopic evolutions; and (4) the occurrence at Bluff and the postmetamorphic, undeformed Pb-Zn-Ag veins and replacements at Hannum, Independence, Foster, and Omilak show the highest values of 206 Pb/ 204 Pb in the region. Pb isotope data for the stratabound Zn-Pb deposits and occurrences do not lie along similar secondary or anomalous lead evolution lines, and there is no shared, two-stage lead line that would provide intersections with a primary or single-stage lead isotope growth curve. Lead isotopic characteristics of the Nelson stratabound deposit and the deformed veins at Quarry and Galena indicate that they largely shared metal and fluid sources. Quarry and Galena also display sufficient Pb isotopic contrast compared to Aurora Creek and Wheeler North to eliminate such veins as subsurface “feeders” for these stratabound deposits, if the deformed veins and deposits formed as closed isotopic systems (without a contribution from externally derived lead). The Pb isotope composition of galena from Aurora Creek formed by a multistage process. It is thus possible that the Aurora Creek deposit originally contained Pb isotope compositions that resembled those from Quarry and Galena. That early-formed Pb was probably remobilized and mixed with radiogenic lead contributed by Mesozoic hydrothermal fluids similar to those associated with the gold-quartz veins in the region. Values of 207 Pb/ 204 Pb and 206 Pb/ 204 Pb from each of the deposits and occurrences plot within the Pb isotope fields of the host metasedimentary rocks and Mesoproterozoic basement rocks of Seward Peninsula; Pb isotope compositions in the deposits thus reflect a local source control. The processes that generated the premetamorphic Zn-Pb(-Ag-Au-Ba-F) sulfide deposits in the Nome Complex differed from those that generated Zn-Pb-Ag deposits in the western Brooks Range, such as the giant Red Dog ore body. Taken as a group, the stratabound lenses and deformed veins in the Nome Complex did not form in a single, widespread, homogeneous hydrothermal system. The Brooks Range deposits, which consist of a range of host rock types and styles of mineralization distributed over a large area, have a high degree of regional Pb isotope homogeneity. The Wheeler North deposit is isotopically similar to Red Dog and related deposits and may have formed in a related hydrothermal system. A preliminary comparison of the Pb isotope compositions of sedimentary-exhalative (SEDEX)–type deposits within the Arctic Alaska–Chukotka terrane and deposits in crustal blocks of Laurussia shows: (1) noteworthy Pb isotopic overlap exists between some of Zn-Pb-Ag deposits in Ireland and the deposits in Arctic Alaska ; but (2) no exact isotopic match exists between any of the deposits in Arctic Alaska and any deposit in crustal blocks involved in the Paleozoic evolution of Laurussia.

Alaska↗

USGS2014

Sulfur and oxygen isotopic study of Paleozoic sediment-hosted Zn-Pb(-Ag-Au-Ba-F) deposits and associated hydrothermal alteration zones in the Nome Complex, Seward Peninsula, Alaska

Results of sulfur and oxygen isotope studies of sedimentary exhalative (SEDEX) Zn-Pb(-Ag-Au-Ba-F) deposits hosted in metamorphosed Paleozoic clastic and carbonate rocks of the Nome Complex, Seward Peninsula, Alaska, are consistent with data for similar deposits worldwide. Stable isotopic studies of the Nome Complex are challenging because the rocks have undergone Mesozoic blueschist- and greenschist-facies metamorphism and deformation at temperatures estimated from 390–490 °C. Studies of sulfur and oxygen isotopes in other areas suggest that, in the absence of chemical and mineralogical evidence for metasomatism, the principal effect of metamorphism is re-equilibration between individual minerals at the temperature of metamorphism, which commonly leads to a narrowing of the overall range of isotope values for a suite of rocks, but generally does not significantly modify the average whole rock value for that suite. Sulfur isotope studies of the stratabound and locally stratiform sulfide lenses at the Aurora Creek-Christophosen deposit, which is of possible Late Devonian-early Carboniferous age, show a large range of δ34Ssulfide values from -9.7 to 39.4‰, suggesting multiple sulfur sources and possibly complex processes of sulfide formation that may include bacterial sulfate reduction, thermochemical sulfate reduction, and Rayleigh distillation. Low δ34S values probably represent bacterial sulfide minerals remobilized from the host metasedimentary rocks either during the original seafloor mineralization or are related to a Cretaceous mineralizing event that produced Au-vein and base-metal replacement deposits; the latter process is supported by Pb isotope data. The Wheeler North deposit is similar to Aurora Creek-Christophosen but does not have negative δ34S values. It also probably formed in an euxinic sub-basin. The stratabound Nelson deposit, and the deformed veins at the Galena and Quarry deposits, may be older than the Aurora Creek-Christophosen and Wheeler North deposits. The Nelson deposit has a lower and narrower range of δ34S values (1.9 to 10.4‰), averaging about 8‰. The Galena and Quarry veins display δ34S values that are similar to those of the stratabound Nelson deposit. Barite samples from the Aurora Creek-Christophosen, Wheeler North, and Quarry deposits have 34S-enriched δ34S values between 25 and 30‰ that are consistent with derivation of the sulfur from coeval (Paleozoic) seawater sulfate. Given their δ34S values, it is likely that the Aurora Creek-Christophosen and Wheeler North deposits formed in closed sub-basins with euxinic conditions that led to extreme Rayleigh distillation to produce the very large range and very high δ34S values. The Nelson deposit probably formed within an anoxic but not euxinic sub-basin. At Nelson, sulfide was likely derived by a subsurface thermochemical sulfate reduction (TSR) reaction, similar to reactions that are inferred to have produced the sulfides in the Galena and Quarry deposits, which are interpreted as feeder veins for the stratabound deposits. Calculations of oxygen isotope temperatures are based on the assumption that evolved seawater with δ18O of 3‰ was the mineralizing and altering fluid related to the formation of the sulfide deposits. Temperatures of aluminous alteration and sulfide mineralization were between 109 and 209 °C, determined on the basis of oxygen isotope fractionations between the mineralizing fluid and proportionate amounts of quartz and muscovite in the rocks. These temperature estimates agree well with known temperatures of SEDEX mineralization worldwide. Sulfur isotope values also are generally consistent with the known ranges in SEDEX deposits worldwide (δ34S ≈ -5 to 25‰).

GSA Special Papers↗

USGS2014

The geobiology of sediment-hosted mineral deposits

The role of biological processes in the formation of sediment-hosted ore deposits has long been recognized. In this review, we focus on the biogeochemical cycling of C, Mn, Fe, and S as they relate to the formation of sediment-hosted Mn and Fe deposits, metalliferous black shales, clastic-dominated (CD) Pb-Zn deposits, and phosphorites. Biological mediation of ore-forming processes occurs over large spans of space and time. The most important step is oxygenic photosynthesis, a biological innovation dating from the Archean Eon that releases free oxygen into the surface oceans and atmosphere and delivers chemical potential, in the form of reduced carbon, to the seafloor. Photosynthetic oxygen is available to precipitate dissolved Fe 2 + and Mn 2 +, and therefore it augments the formation of sedimentary Mn and Fe deposits, and drives oxidative weathering of exposed crust, thereby delivering sulfate and transition metals to the ocean. Where reduced carbon accumulates in the deep oceans and on the seafloor, bacterial sulfate reduction produces hydrogen sulfide thereby facilitating the formation of metalliferous black shales, sediment-hosted Pb and Zn sulfide deposits, and phosphorites. Thus, an understanding of major biogeochemical processes and how they have evolved over time is required in order to refine genetic models for sediment-hosted ore deposits and to guide future mineral exploration. A close secular relationship between deposit formation and trends in major biogeochemical cycles provides a potentially powerful tool for mineral resource assessment. Sedimentary basins that formed during a time that is known to lack deposits of a particular metal can be eliminated during exploration programs, whereas others of permissive ages should be considered priorities. For example, sedimentary basins older than ca. 1.8 Ga are unlikely to contain large CD Pb-Zn deposits, and basins that formed between 1.6 and 0.6 Ga are not prospective for phosphorites. Recent technological advances in the application of nanometer-, micron-, and bulk-scale analytical techniques allow for imaging of complex biological structures and have provided new insights into the role of bacteria, not only in direct formation of mineral deposits, but also in leaching of metals from ore and mineralized rocks. Future exploration for, and exploitation of, mineral deposits may include offshore or land-based, low-grade, high-tonnage targets; understanding the role of bacteria in mineral growth, mineral dissolution, and redox transformations will aid in predicting where such deposits exist, and how metal extraction from ores can be enhanced.

Book chapter↗

USGS2013

Descriptive and geoenvironmental model for Co-Cu-Au deposits in metasedimentary rocks

Introduction This report is a revised model for a specific type of cobalt-copper-gold (Co-Cu-Au) deposit that will be evaluated in the next U.S. Geological Survey (USGS) assessment of undiscovered mineral resources in the United States (see Ferrero and others, 2012). Emphasis is on providing an up-to-date deposit model that includes both geologic and geoenvironmental aspects. The new model presented here supersedes previous USGS models by Earhart (1986) and Evans and others (1995), which are based solely on deposits in the Blackbird mining district of central Idaho. This report is a broader synthesis of information on 19 Co-Cu-Au deposits occurring in predominantly metasedimentary successions worldwide (table 1–1) that generally share common geologic, mineralogical, and geochemical features; preliminary summary versions were presented in Slack and others (2010) and Slack and others (2011), which are superseded by this report. As defined herein, the individual Co-Cu-Au deposits are located more than 500 meters from similar deposits and contain 0.1 percent or more by weight of Co in ore or mineralized rock; some deposits included in the database lack reported average Co grades, but they contain high Co concentrations, at least locally. Most of the deposits also have high As contents, present in Co arsenide and sulfarsenide minerals. Type examples of the Co-Cu-Au deposits are those in the Blackbird district, Skuterud in Norway, and Kouvervarra and Juomasuo in Finland. Some deposits in the database have low grades for Cu (for example, NICO in Canada) or Au (for example, Lemmonlampi in Finland), but these deposits are included because their geological, mineralogical, and alteration features are similar to those of the type examples. Several deposits included in the model are partly hosted by metavolcanic or metaigneous rocks (including granite), but regionally these deposits are within metasedimentary successions; no deposits are wholly within granite or other plutonic igneous intrusions. Despite having a lower average Co grade, the Mt. Cobalt deposit in Australia is included here because it has past Co production from higher-grade ore zones (Nisbet and others, 1983). The Black Pine deposit in the Idaho cobalt belt is included because it contains mineable Co- and Au-rich lenses within Cu-rich mineralized zones (Formation Metals, Inc., 2012). Six deposits that lack data for average Co grades are also included because each reportedly contains abundant Co (>0.1 weight percent Co), at least locally. Many of the deposits are noteworthy as possible resources of Ag, Bi, W, Ni, Y, REE, and (or) U. Detailed data on the deposits listed in table 1–1, including references, are available in appendix 1. Significantly, the grouping in this report of Co-Cu-Au deposits in metasedimentary rocks into a single model includes deposits that other workers have previously classified in different ways. For background information, a global overview of different types of Co deposits worldwide is given in Smith (2001). Additional geologically and compositionally similar deposits are known, but have average Co grades less than 0.1 percent. Most of these deposits contain cobalt-rich pyrite and lack appreciable amounts of distinct Co sulfide and (or) sulfarsenide minerals. Such deposits are not discussed in detail in the following sections, but these deposits may be relevant to the descriptive and genetic models presented below. Examples include the Scadding Au-Co-Cu deposit in Ontario, Canada; the Vähäjoki Co-Cu-Au deposit in Finland; the Tuolugou Co-Au deposit in Qinghai Province, China; the Lala Co-Cu-UREE deposit in Sichuan Province, China; the Guelb Moghrein Cu-Au-Co deposit in Mauritania; and the Great Australia Co-Cu, Greenmount Cu-Au-Co, and Monakoff Cu-Au-Co-UAg deposits in Queensland, Australia. Detailed information on these deposits is presented in appendix 2.

Scientific Investigations Report↗

USGS2012

Sulfur, carbon, hydrogen, and oxygen isotope geochemistry of the Idaho cobalt belt

Cobalt-copper ± gold deposits of the Idaho cobalt belt, including the deposits of the Blackbird district, have been analyzed for their sulfur, carbon, hydrogen, and oxygen isotope compositions to improve the understanding of ore formation. Previous genetic hypotheses have ranged widely, linking the ores to the sedimentary or diagenetic history of the host Mesoproterozoic sedimentary rocks, to Mesoproterozoic or Cretaceous magmatism, or to metamorphic shearing. The δ 34 S values are nearly uniform throughout the Blackbird dis- trict, with a mean value for cobaltite (CoAsS, the main cobalt mineral) of 8.0 ± 0.4‰ ( n = 19). The data suggest that (1) sulfur was derived at least partly from sedimentary sources, (2) redox reactions involving sulfur were probably unimportant for ore deposition, and (3) the sulfur was probably transported to sites of ore for- mation as H 2 S. Hydrogen and oxygen isotope compositions of the ore-forming fluid, which are calculated from analyses of biotite-rich wall rocks and tourmaline, do not uniquely identify the source of the fluid; plausible sources include formation waters, metamorphic waters, and mixtures of magmatic and isotopically heavy meteoric waters. The calculated compositions are a poor match for the modified seawaters that form vol- canogenic massive sulfide (VMS) deposits. Carbon and oxygen isotope compositions of siderite, a mineral that is widespread, although sparse, at Blackbird, suggest formation from mixtures of sedimentary organic carbon and magmatic-metamorphic carbon. The isotopic compositions of calcite in alkaline dike rocks of uncertain age are consistent with a magmatic origin. Several lines of evidence suggest that siderite postdated the emplacement of cobalt and copper, so its significance for the ore-forming event is uncertain. From the stable isotope perspective, the mineral deposits of the Idaho cobalt belt contrast with typical VMS and sedimentary exhalative deposits. They show characteristics of deposit types that form in deeper environments and could be related to metamorphic processes or magmatic processes, although the isotopic evidence for magmatic components is relatively weak.

Idaho↗

USGS2012

Volcanogenic massive sulfide occurrence model

Volcanogenic massive sulfide deposits, also known as volcanic-hosted massive sulfide, volcanic-associated massive sulfide, or seafloor massive sulfide deposits, are important sources of copper, zinc, lead, gold, and silver (Cu, Zn, Pb, Au, and Ag). These deposits form at or near the seafloor where circulating hydrothermal fluids driven by magmatic heat are quenched through mixing with bottom waters or porewaters in near-seafloor lithologies. Massive sulfide lenses vary widely in shape and size and may be podlike or sheetlike. They are generally stratiform and may occur as multiple lenses. Volcanogenic massive sulfide deposits range in size from small pods of less than a ton (which are commonly scattered through prospective terrains) to supergiant accumulations like Rio Tinto (Spain), 1.5 billion metric tons; Kholodrina (Russia), 300 million metric tons; Windy Craggy (Canada), 300 million metric tons; Brunswick No. 12 (Canada), 230 million metric tons; and Ducktown (United States), 163 million metric tons. Volcanogenic massive sulfide deposits range in age from 3.55 billion years to zero-age deposits that are actively forming in extensional settings on the seafloor, especially mid-ocean ridges, island arcs, and back-arc spreading basins. The widespread recognition of modern seafloor Volcanogenic massive sulfide deposits and associated hydrothermal vent fluids and vent fauna has been one of the most astonishing discoveries in the last 50 years, and seafloor exploration and scientific studies have contributed much to our understanding of ore-forming processes and the tectonic framework for volcanogenic massive sulfide deposits in the marine environment. Massive ore in volcanogenic massive sulfide deposits consists of greater than 40 percent sulfides, usually pyrite, pyrrhotite, chalcopyrite, sphalerite, and galena; non-sulfide gangue typically consists of quartz, barite, anhydrite, iron oxides, chlorite, sericite, talc, and their metamorphosed equivalents. Ore composition may be Pb-Zn-, Cu-Zn-, or Pb-Cu-Zn-dominated, and some deposits are zoned vertically and laterally. Many deposits have stringer or feeder zones beneath the massive zone that consist of crosscutting veins and veinlets of sulfides in a matrix of pervasively altered host rock and gangue. Alteration zonation in the host rocks surrounding the deposits are usually well-developed and include advanced argillic (kaolinite, alunite), argillic (illite, sericite), sericitic (sericite, quartz), chloritic (chlorite, quartz), and propylitic (carbonate, epidote, chlorite) types. An unusual feature of VMS deposits is the common association of stratiform "exhalative" deposits precipitated from hydrothermal fluids emanating into bottom waters. These deposits may extend well beyond the margins of massive sulfide and are typically composed of silica, iron, and manganese oxides, carbonates, sulfates, sulfides, and tourmaline.

Scientific Investigations Report↗

USGS2011

Whole-rock and sulfide-mineral geochemical data for samples from volcanogenic massive sulfide deposits of the Bonnifield district, east-central Alaska

This Open-File Report presents geochemical data for outcrop and drill-core samples from volcanogenic massive sulfide deposits and associated metaigneous and metasedimentary rocks in the Wood River area of the Bonnifield mining district, northern Alaska Range, east-central Alaska. The data consist of major- and trace-element whole-rock geochemical analyses, and major- and trace-element analyses of sulfide minerals determined by electron microprobe and laser ablation—inductively coupled plasma—mass spectrometry (LA-ICP-MS) techniques. The PDF consists of text, appendix explaining the analytical methods used for the analyses presented in the data tables, a sample location map, and seven data tables. The seven tables are also available as spreadsheets in several file formats. Descriptions and discussions of the Bonnifield deposits are given in Dusel-Bacon and others (2004, 2005, 2006, 2007, 2010).

Alaska↗

USGS2011

Depositional setting and geochemistry of phosphorites and metalliferous black shales in the Carboniferous-Permian Lisburne Group, Northern Alaska

Phosphatic rocks are distributed widely in the Lisburne Group, a mainly Carboniferous carbonate succession that occurs throughout northern Alaska. New sedimentologic, paleontologic, and geochemical data presented here constrain the geographic and stratigraphic extent of these strata and their depositional and paleogeographic settings. Our findings support models that propose very high oxygen contents of the Permo-Carboniferous atmosphere and oceans, and those that suggest enhanced phosphogenesis in iron-limited sediments; our data also have implications for Carboniferous paleogeography of the Arctic. Lisburne Group phosphorites range from granular to nodular, are interbedded with black shale and lime mudstone rich in radiolarians and sponge spicules, and accumulated primarily in suboxic outer- to middle-ramp environments. Age constraints from conodonts, foraminifers, and goniatite cephalopods indicate that most are middle Late Mississippian (early Chesterian; early late Visean). Phosphorites form 2- to 40-cm-thick beds of sand- to pebble-sized phosphatic peloids, coated grains, and (or) bioclasts cemented by carbonate, silica, or phosphate that occur through an interval =12 m thick. High gamma-ray response through this interval suggests strongly condensed facies related to sediment starvation and development of phosphatic hardgrounds. Phosphorite textures, such as unconformity-bounded coated grains, record multiple episodes of phosphogenesis and sedimentary reworking. Sharp bed bases and local grading indicate considerable redeposition of phosphatic material into deeper water by storms and (or) gravity flows. Lisburne Group phosphorites contain up to 37 weight percent P2O5, 7.6 weight percent F, 1,030 ppm Y, 517 ppm La, and 166 ppm U. Shale-normalized rare earth element (REE) plots show uniformly large negative Ce anomalies Ce/Ce*=0.11 + or - 0.03) that are interpreted to reflect phosphate deposition in seawater that was greatly depleted in Ce due to increased oxygenation of the atmosphere and oceans during the Carboniferous evolution of large vascular land plants. Black shales within the phosphorite sections have up to 20.2 weight percent Corg and are potential petroleum source rocks. Locally, these strata also are metalliferous, with up to 1,690 ppm Cr, 2,831 ppm V, 551 ppm Ni, 4,670 ppm Zn, 312 ppm Cu, 43.5 ppm Ag, and 12.3 ppm Tl; concentrations of these metals covary broadly with Corg, suggesting coupled redox variations. Calculated marine fractions (MF) of Cr, V, and Mo, used to evaluate the paleoredox state of the bottom waters, show generally high CrMF/MoMF and VMF/MoMF ratios that indicate deposition of the black shales under suboxic denitrifying conditions; Re/Mo ratios also plot mainly within the suboxic field and support this interpretation. Predominantly seawater and biogenic sources are indicated for Cr, V, Mo, Zn, Cd, Ni, and Cu in the black shales, with an additional hydrothermal contribution inferred for Zn, Cd, Ag, and Tl in some samples. Lisburne Group phosphorites formed in the Ikpikpuk Basin and along both sides of the mud- and chert-rich Kuna Basin, which hosts giant massive sulfide and barite deposits of the Red Dog district. Lisburne Group phosphatic strata are coeval with these deposits and formed in response to a nutrient-rich upwelling regime. Phosphate deposition occurred mainly in suboxic bottom waters based on data for paleoredox proxies (Cr, V, Mo, Re) within contemporaneous black shales. Recent global reconstructions are consistent with Carboniferous upwelling in northern Alaska, but differ in the type of upwelling expected (zonal versus meridional). Paleoenvironmental data suggest that meridional upwelling may better explain phosphorite deposition in the Lisburne Group.

Alaska↗