The Nome Complex is a large metamorphic unit that sits along the southern boundary of the Arctic Alaska–Chukotka terrane, the largest of several microcontinental 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.

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.

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.

Results of sulfur and oxygen isotopic 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 greenschistfacies metamorphism and deformation at temperatures estimated from 390 to 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 isotopic 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 δ 34 S sulfide 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 in a restricted sulfide basin, and Rayleigh distillation. Low δ 34 S 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 δ 34 S values. It probably formed in an euxinic subbasin. 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 δ 34 S values (1.9‰–10.4‰), averaging ~8‰. The Galena and Quarry vein deposits display δ 34 S values that are similar to those of the stratabound Nelson deposit. Barite samples from the Aurora Creek–Christophosen, Wheeler North, and Quarry deposits have 34 S-enriched δ 34 S values between 25‰ and 30‰ that are consistent with derivation of the sulfur from coeval (Paleozoic) seawater sulfate. Given their δ 34 S values, it is likely that the Aurora Creek–Christophosen and Wheeler North deposits formed in closed subbasins with euxinic conditions that led to extreme Rayleigh distillation to produce the very large range and very high δ 34 S values. The Nelson deposit probably formed within an anoxic but not euxinic subbasin. 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 δ 18 O 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 (δ 34 S ≈ −5‰ to 25‰).

Abstract 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.

Abstract 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.