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D. L. Leach

Publications and source records attributed to D. L. Leach.

At least 19 recordsLinked to original sources
USGS2009

Genesis of the Assif El Mal Zn-Pb (Cu, Ag) vein deposit. An extension-related Mesozoic vein system in the High Atlas of Morocco. Structural, mineralogical, and geochemical evidence

The Assif El Mal Zn-Pb (Cu-Ag) vein system, located in the northern flank of the High Atlas of Marrakech (Morocco), is hosted in a Cambro-Ordovician volcaniclastic and metasedimentary sequence composed of graywacke, siltstone, pelite, and shale interlayered with minor tuff and mudstone. Intrusion of synorogenic to postorogenic Late Hercynian peraluminous granitoids has contact metamorphosed the host rocks giving rise to a metamorphic assemblage of quartz, plagioclase, biotite, muscovite, chlorite, amphibole, chloritoid, and garnet. The Assif El Mal Zn-Pb (Cu-Ag) mineralization forms subvertical veins with ribbon, fault breccia, cockade, comb, and crack and seal textures. Two-phase liquid-vapor fluid inclusions that were trapped during several stages occur in quartz and sphalerite. Primary inclusion fluids exhibit T h mean values ranging from 104??C to 198??C. Final ice-melting temperatures range from -8.1??C to -12.8??C, corresponding to salinities of ???15 wt.% NaCl equiv. Halogen data suggest that the salinity of the ore fluids was largely due to evaporation of seawater. Late secondary fluid inclusions have either Ca-rich, saline (26 wt.% NaCl equiv.), or very dilute (3.5 wt.% NaCl equiv.) compositions and homogenization temperatures ranging from 75??C to 150??C. The ?? 18 O and ??D fluid values suggest an isotopically heterogeneous fluid source involving mixing between connate seawater and black-shale-derived organic waters. Low ?? 13 C VPDB values ranging from -7.5??? to -7.7??? indicate a homogeneous carbon source, possibly organic matter disseminated in black shale hosting the Zn-Pb (Cu-Ag) veins. The calculated ?? 34 S H2S values for reduced sulfur (22.5??? to 24.3???) are most likely from reduction of SO 4 2- in trapped seawater sulfate or evaporite in the host rocks. Reduction of sulfate probably occurred through thermochemical sulfate reduction in which organic matter was oxidized to produce CO 2 which ultimately led to precipitation of saddle dolomite with isotopically light carbon. Lead isotope compositions are consistent with fluid-rock interaction that leached metals from the immediate Cambro-Ordovician volcaniclastic and metasedimentary sequence or from the underlying Paleo-Neoproterozoic crustal basement. Geological constraints suggest that the vein system of Assif El Mal formed during the Jurassic opening of the central Atlantic Ocean. ?? Springer-Verlag 2009.

Mineralium Deposita↗
USGS2008

Reactive flow models of the Anarraaq Zn-Pb-Ag deposit, Red Dog district, Alaska

The Red Dog ore deposit district in the Brooks Range of northern Alaska is host to several high-grade, shale-hosted Zn + Pb deposits. Due to the complex history and deformation of these ore deposits, the geological and hydrological conditions at the time of formation are poorly understood. Using geological observations and fluid inclusion data as constraints, numerical heat and fluid flow simulations of the Anarraaq ore deposit environment and coupled reactive flow simulations of a section of the ore body were conducted to gain more insight into the conditions of ore body formation. Results suggest that the ore body and associated base metal zonation may have formed by the mixing of oxidized, saline, metal-bearing hydrothermal fluids (<200??C) with reducing, HS-rich pore fluids within radiolarite-rich host rocks. Sphalerite and galena concentrations and base metal sulfide distribution are primarily controlled by the nature of the pore fluids, i.e., the extent and duration of the HS- source. Forward modeling results also predict the distribution of pyrite and quartz in agreement with field observations and indicate a reaction front moving from the initial mixing interface into the radiolarite rocks. Heuristic mass calculations suggest that ore grades and base metal accumulation comparable to those found in the field (18% Zn, 5% Pb) are predicted to be reached after about 0.3 My for initial conditions (30 ppm Zn, 3 ppm Pb; 20% deposition efficiency). ?? Springer-Verlag 2008.

Mineralium Deposita↗
USGS2004

Sulfur and oxygen isotopes in barite deposits of the western Brooks Range, Alaska, and implications for the origin of the Red Dog massive sulfide deposits

Sulfur and oxygen isotope analyses have been obtained for barite samples from the giant stratiform sulfide barite deposits at Red Dog in the western Brooks Range of Alaska, from stratiform barite deposits elsewhere in the Red Dog district, and from stratiform and vein and breccia barite occurrences in the central Brooks Range. Twelve of the 15 deposits studied lie within middle to Upper Mississippian black shale and chert units. The data reveal two different patterns on ?? 34S versus ??18O plots. The first, which is best illustrated by the barite deposit at Anarraaq, shows linear trends with slopes that vary with barite texture. For most samples, ??34S and ??18O values are both higher than the values characteristic of Mississippian marine sulfate. The second pattern, which is evident at the Red Dog deposits, shows no correlation between ??34S and ??18. In most samples, ??18O is below the value for Mississippian marine sulfate. Comparisons with sulfate in modern marine environments suggest a possible model for the mineralizing process. Anarraaq-type barite formed at sea-floor vents where ascending fluids carrying barium and methane encountered sulfate-bearing pore waters or bottom waters. Barite deposition was accompanied by the reduction of sulfate to H2S by means of microbially mediated anaerobic methane oxidation. Red Dog-type barite was formed in a manner similar to Anarraaq-type barite but was over-printed by a massive sulfide-forming event. Red Dog sulfides precipitated where metal-bearing hydrothermal fluids encountered pore waters that had been charged with H2S by anaerobic methane oxidation. Textural and isotopic evidence indicates that the sulfide bodies grew by consuming the available H2S and then by reductively dissolving barite. Dissolution of barite caused barium to be released to higher stratigraphic levels where it was reprecipitated on encountering sulfate. Isotopic evidence is pre sented for a link between methane venting and barite formation and raises the possibility that the coexistence of barite and sulfide at Red Dog, and the occurrence elsewhere in the district of barite-only and sulfide-only deposits, can be explained by a spectrum of vent types in the Mississippian basin analogous to the spectrum that is observed today along the modern continental margins. Authigenic barite formed at some but not all methane seeps, perhaps owing to differences in the barium content of vent fluids, differences in the relative proportion of aqueous fluid and gas emanating from vents, or differences in sulfate availability in local bottom waters. Some barite-forming seeps were later replaced by sulfides (Red Dog deposits) whereas others were not (e.g., Anarraaq barite horizon, Gull Creek, Moil). At sulfide occurrences where there is little evidence of preexisting barite (e.g., Anarraaq, Wulik, Suds), methane venting is indicated by fossils suggestive of chemosynthetic fauna. Mammiform sedimentary structures that are widespread in black chert at the top of the Kuna Formation may represent seeps that supported neither authigenic mineral formation nor chemosynthetic megafauna. ?? 2004 by Economic Geology.

Economic Geology↗
USGS2004

Textural, compositional, and sulfur isotope variations of sulfide minerals in the Red Dog Zn-Pb-Ag deposits, Brooks Range, Alaska: Implications for Ore Formation

The Red Dog Zn-Pb deposits are hosted in organic-rich mudstone and shale of the Mississippian Kuna Formation. A complex mineralization history is defined by four sphalerite types or stages: (1) early brown sphalerite, (2) yellow-brown sphalerite, (3) red-brown sphalerite, and (4) late tan sphalerite. Stages 2 and 3 constitute the main ore-forming event and are volumetrically the most important. Sulfides in stages 1 and 2 were deposited with barite, whereas stage 3 largely replaces barite. Distinct chemical differences exist among the different stages of sphalerite. From early brown sphalerite to later yellow-brown sphalerite and red-brown sphalerite, Fe and Co content generally increase and Mn and Tl content generally decrease. Early brown sphalerite contains no more than 1.9 wt percent Fe and 63 ppm Co, with high Mn (up to 37 ppm) and Tl (126 ppm), whereas yellow-brown sphalerite and red-brown sphalerite contain high Fe (up to 7.3 wt %) and Co (up to 382 ppm), and low Mn (<27 ppm) and Tl (<37 ppm). Late tan sphalerite has distinctly lower Fe (< 0.9 wt %) and higher Tl (up to 355 ppm), Mn (up to 177 ppm), and Ge (426 ppm), relative to earlier sphalerite. Wide ranges in concentrations of Ag, Cu, Pb, and Sb characterize all sphalerite types, particularly yellow-brown sphalerite and red-brown sphalerite, and most likely reflect submicroscopic inclusions of galena, chalcopyrite and/or tetrahedrite in the sphalerite. In situ ion microprobe sulfur isotope analyses show a progression from extremely low ??34S values for stage 1 (as low as -37.20???) to much higher values for yellow-brown sphalerite (mean of 3.3???; n = 30) and red-brown sphalerite (mean of 3.4; n = 20). Late tan sphalerite is isotopically light (-16.4 to -27.2???). The textural, chem ical, and isotopic data indicate the following paragenesis: (1) deposition of early brown sphalerite with abundant barite, minor pyrite, and trace galena immediately beneath the sea floor in unconsolidated mud; (2) deposition of yellow-brown sphalerite during subsea-floor hydrothermal recrystallization and coarsening of preexisting barite; (3) open-space deposition of barite, red-brown sphalerite and other sulfides in veins and coeval replacement of barite; and (4) postore sulfide deposition, including the formation of late tan sphalerite breccias. Stage 1 mineralization took place in a low-temperature environment where fluids rich in Ba mixed with pore water or water-column sulfate to form barite, and metals combined with H2S derived from bacterial sulfate reduction to form sulfides. Higher temperatures and salinities and relatively oxidized ore-stage fluids (stages 2 and 3) compared with stage 1 were probably important controls on the abundances and relative amounts of metals in the fluids and the resulting sulfide chemistry. Textural observations and isotopic data show that preexisting barite was reductively dissolved, providing a source of H2S for sulfide mineral formation. In stage 3, the continued flow of hydrothermal fluids caused thermal alteration of organic-rich mudstones and a build-up of methane that led to fluid overpressuring, hydrofracturing, and vein formation. Barite, red-brown sphalerite, and other sulfides were deposited in the veins, and preexisting barite was pervasively replaced by red-brown sphalerite. Hydrothermal activity ceased until Jurassic time when thrusting and large-scale fluid flow related to the Brookian orogeny remobilized and formed late tan sphalerite in tectonic breccias. ?? 2004 by Economic Geology.

Economic Geology↗
USGS2004

Paleomagnetism of the Red Dog Zn-Pb massive sulfide deposit in northern Alaska

Paleomagnetic methods have isolated two ancient magnetizations in and around the Paleozoic shale-hosted Red Dog ore deposit in northern Alaska. A high-latitude, westerly magnetization carried by magnetite, termed characteristic remanent magnetization A, was found in rocks that have barite and/or substantial quartz replacement of barite. An intermediate- to low-latitude, southerly magnetization (characteristic remanent magnetization B) is carried by pyrrhotite and was found in rocks dominated by galena and sphalerite. The ages the two components are constrained by their relationship with geochemistry, radiometric age dating, and hypotheses for the Mesozoic tectonic history of the Brooks Range. Characteristic remanent magnetization A fails the fold test so it must postdate the end of Brookian orogenesis (??? 150 Ma). It is always found with replacement quartz that has a radiometric date (white mica from a vug, 39Ar/40Ar) of 126 Ma. The paleolatitude for characteristic remanent magnetization B is too shallow to be Mesozoic or younger, regardless of the model for the tectonic origin of northern Alaska, and must predate Brookian orogenesis. Geologic mapping suggests that most of the ore is syngenetic, formed at 330 to 340 Ma, and a radiometric date (Re-Os on pyrite) yields an age of 338 Ma. Since characteristic remanent magnetization B predates deformation, is found in mineralized rocks and is carried by pyrrhotite, it was probably acquired during the mineralizing process as well. The combined radiometric ages and paleomagnetic data sets can be best interpreted by assuming that northern Alaska was part of an accreted terrane that was translated northward by about 30?? into its current location relative to the rest of North America and then rotated counterclockwise by 50?? to 70??. This tectonic interpretation yields plausible magnetization ages for both characteristic remanent magnetization A and B. Geologic evidence, isotopic ages, and paleomagnetic data indicate formation of the deposit at a paleolatitude that is much lower than today. ?? 2004 by Economic Geology.

Economic Geology↗
USGS2004

Re-Os sulfide geochronology of the Red Dog sediment-hosted Zn-Pb-Ag deposit, Brooks Range, Alaska

The Red Dog sediment-hosted deposit in the De Long Mountains of northern Alaska is the largest Zn producer in the world. Main stage mineralization is characterized by massive sulfide ore and crosscutting subvertical veins. Although the vein mineralization is clearly younger than the massive ore, the exact temporal relationship between the two is unclear. Re-Os geochronology of pyrite is used to determine the absolute age of main stage ore at Red Dog. A 10-point isochron on both massive and vein pyrite yields an age of 338.3 ?? 5.8 Ma and is interpreted to represent the age of main stage ore. The Re-Os data indicate that both massive and vein ore types are coeval within the resolution of the technique. Formation of the Red Dog deposit was associated with extension along a passive continental margin, and therefore the Re-Os age of main stage ore constrains the timing of rifting as well as the age of the host sedimentary rocks. Sphalerite from both massive and vein ore yields imprecise ages and shows a high degree of scatter compared to pyrite. We suggest that the Re-Os systematics of sphalerite can be disturbed and that this mineral is not reliable for Re-Os geochronology. ?? 2004 by Economic Geology.

Economic Geology↗
USGS2003

Tectonic controls of Mississippi Valley-type lead-zinc mineralization in orogenic forelands

Most of the world's Mississippi Valley-type (MVT) zinc-lead deposits occur in orogenic forelands. We examine tectonic aspects of foreland evolution as part of a broader study of why some forelands are rich in MVT deposits, whereas others are barren. The type of orogenic foreland (collisional versus Andean-type versus inversion-type) is not a first-order control, because each has MVT deposits (e.g., Northern Arkansas, Pine Point, and Cevennes, respectively). In some MVT districts (e.g., Tri-State and Central Tennessee), mineralization took place atop an orogenic forebulge, a low-amplitude (a few hundred meters), long-wavelength (100-200 km) swell formed by vertical loading of the foreland plate. In the foreland of the active Banda Arc collision zone, a discontinuous forebulge reveals some of the physiographic and geologic complexities of the forebulge environment, and the importance of sea level in determining whether or not a forebulge will emerge and thus be subject to erosion. In addition to those on extant forebulges, some MVT deposits occur immediately below unconformities that originated at a forebulge, only to be subsequently carried toward the orogen by the plate-tectonic conveyor (e.g., Daniel's Harbour and East Tennessee). Likewise, some deposits are located along syn-collisional, flexure-induced normal and strike-slip faults in collisional forelands (e.g., Northern Arkansas, Daniel's Harbour, and Tri-State districts). These findings reveal the importance of lithospheric flexure, and suggest a conceptual tectonic model that accounts for an important subset of MVT deposits-those in the forelands of collisional orogens. The MVT deposits occur both in flat-lying and in thrust-faulted strata; in the latter group, mineralization postdated thrusting in some instances (e.g., Picos de Europa) but may have predated thrusting in other cases (e.g., East Tennessee).

Mineralium Deposita↗
USGS2003

Coupled heat and fluid flow modeling of the Carboniferous Kuna Basin, Alaska: Implications for the genesis of the Red Dog Pb-Zn-Ag-Ba ore district

The Red Dog deposit is a giant 175 Mton (16% Zn, 5% Pb), shale-hosted Pb-Zn-Ag-Ba ore district situated in the Carboniferous Kuna Basin, Western Brooks Range, Alaska. These SEDEX-type ores are thought to have formed in calcareous turbidites and black mudstone at elevated sub-seafloor temperatures (120-150??C) within a hydrogeologic framework of submarine convection that was structurally organized by large normal faults. The theory for modeling brine migration and heat transport in the Kuna Basin is discussed with application to evaluating flow patterns and heat transport in faulted rift basins and the effects of buoyancy-driven free convection on reactive flow and ore genesis. Finite element simulations show that hydrothermal fluid was discharged into the Red Dog subbasin during a period of basin-wide crustal heat flow of 150-160 mW/m2. Basinal brines circulated to depths as great as 1-3 km along multiple normal faults flowed laterally through thick clastic aquifers acquiring metals and heat, and then rapidly ascended a single discharge fault zone at rates ??? 5 m/year to mix with seafloor sulfur and precipitate massive sulfide ores. ?? 2003 Elsevier Science B.V. All rights reserved.

Conference Paper↗
USGS1998

Evidence for Proterozoic and late Cretaceous-early Tertiary ore-forming events in the Coeur d'Alene district, Idaho and Montana

New 40 Ar/ 39 Ar age spectra on sericite and lead isotope data on tetrahedrite, siderite, galena, bournonite, and stibnite, together with previously published isotopic, geochemical, and geologic studies provide evidence for two major vein-forming events in the Coeur d'Alene district and surrounding areas of the Belt basin. The data suggest that the zinc- and lead-rich veins (e.g., Bunker Hill and Star-Morning mines) formed in the Proterozoic (1.0 Ga), whereas the silver-rich veins (e.g., Silver belt mines), antimony veins (e.g., U.S. Antimony mine), and gold-bearing quartz veins (Murry subdistrict) formed in Late Cretaceous to early Tetitary time.

Economic Geology↗
USGS1997

Evidence for hot Mississippi Valley-type brines in the Reelfoot Rift complex, south-central United States, in Late Pennsylvanian-Early Permian

Petrographic and fluid inclusion studies of sparry dolomite cement from Upper Cambrian to Lower Ordovician rocks and conodont thermal-alteration indices provide evidence that hot mississippi valley-type brines were once present in the Reelfoot Rift complex. The cathodoluminescent microstratigraphy of sparry dolomite cement in the Reelfoot Rift resembles that of sparry dolomite cement associated with widespread mississippi valley-type deposition in the Ozark region. If correlative cathodoluminescent zones in the sparry dolomite from the Ozark and Reelfoot Rift regions indicate broadly contemporaneous dolomite deposition, then the results show that the Ozark MVT-type hydrothermal system extended into the Reelfoot region and onto the western flank of the Nashville Dome. Independent evidence supports migration of MVT-type brines into the Ozark region from the Reelfoot Rift complex in late Paleozoic time.

Professional Paper↗
USGS1996

Paragenetic and minor- and trace-element studies of Mississippi Valley-type ore deposits of the Silesian-Cracow district, Poland

Paragenetic and minor- and trace-element studies were conducted on samples of epigenetic ore and gangue minerals collected from mines and drill core in the Silesian-Cracow (S-C) district of southern Poland. Four discrete mineral suites representing four mineralizing stages can be identified throughout the district. The earliest epigenetic minerals deposited during stage 1 consist of a late dolomite cement together with minor pyrite and marcasite. Stage 2 was the first ore-forming stage and included repetitive deposition of sphalerite and galena in a variety of morphologies. Stage 3 abruptly followed the first ore stage and deposited marcasite and pyrite with variable amounts of late sphalerite and galena. In the samples studied, minerals deposited during stage 3 are predominately marcasite-pyrite with minor sphalerite and galena in the Pomorzany and Olkusz mines, whereas, at the Trzebionka mine, stage 3 mineralization deposited mostly galena and sphalerite with little marcasite or pyrite. Stage 4 minerals include contains barite, followed by calcite, with very minor pyrite and a rare, late granular sphalerite. Compared to other major Mississippi Valley-type (MVT) districts of the world, the Silesian-Cracow district contains sphalerite with the second largest range in Ag concentrations and the largest range in Fe and Cd concentrations of any district. Unlike in other districts, very wide ranges in minor- and trace-element concentrations are also observed in paragenetically equivalent samples collected throughout the district. This wide range indicates that the minor- and trace-element content of the ore-forming environment was highly variable, both spatially and temporally, and suggests that the hydrologic system that the ore fluids traversed from their basinal source was very complex. Throughout the district, a significant increase in Tl, Ge, and As concentrations is accompanied by a lightening of sulfur isotopes between stage 2 and stage 3 minerals. This change appears to record a major district-scale hydrologic event that probably reflects the introduction of fluids with significantly different geochemistry than that of earlier ore-forming fluids.

Prace - Panstwowego Instytutu Geologicznego↗
USGS1996

Sulfur isotope geochemistry of ore and gangue minerals from the Silesian-Cracow Mississippi Valley-type ore district, Poland

Studies of the sulfur isotopic composition of ore and gangue minerals from the Silesian-Cracow Zn-Pb district were conducted to gain insights into processes that controlled the location and distribution of the ore deposits. Results of this study show that minerals from the Silesian-Cracow ore district have the largest range of sulfur isotope compositions in sulfides observed from any Mississippi Valley-type ore district in the world. The ??34S values for sulfide minerals range from +38 to -32 per mil for the entire paragenetic sequence but individual stages exhibit smaller ranges. There is a well developed correlation between the sulfur isotope composition and paragenetic stage of ore deposition. The first important ore stage contains mostly positive ??34S values, around 5 per mil. The second stage of ore formation are lower, with a median value of around -5 to -15 per mil, and with some values as low as -32 per mil. Late stage barite contains isotopically heavy sulfur around +32 per mil. The range in sulfur isotope compositions can be explained by contributions of sulfur from a variety of source rocks together with sulfur isotope fractionations produced by the reaction paths for sulfate reduction. Much of the variation in sulfur isotope compositions can be explained by bacterial reduction of sedimentary sulfate and disequilibrium reactions by intermediate-valency sulfur species, especially in the late-stage pyrite and sphalerite. Organic reduction of sulfate and thermal release of sulfur from coals in the Upper Silesian Coal Basin may have been important contributors to sulfur in the ore minerals. The sulfur isotopic data, ore mineral textures, and fluid inclusion data, are consistent with the hypothesis that fluid mixing was the dominant ore forming mechanism. The rather distinct lowering of ?? 34S values in sulfides from stage 2 to stage 3 is believed to reflect some fundamental change in the source of reduced sulfur and/or hydrology of the ore-forming environment. A change in the hydrology of the ore forming environment could be accomplished by extensional faulting that was coeval with ore formation. Late stage barite contains high values of ??34S which may reflect the final collapse of the hydrothermal system.

Prace - Panstwowego Instytutu Geologicznego↗
USGS1994

Chemical reaction path modeling of ore deposition in Mississippi Valley-type Pb-Zn deposits of the Ozark region, US midcontinent

The Ozark region of the U.S. midcontinent is host to a number of Mississippi Valley-type districts, including the world-class Viburnum Trend, Old Lead Belt, and Tri-State districts and the smaller Southeast Missouri barite, Northern Arkansas, and Central Missouri districts. There is increasing evidence that the Ozark Mississippi Valley-type districts formed locally within a large, interconnected hydrothermal system that also produced broad fringing areas of trace mineralization, extensive subtle hydrothermal alteration, broad thermal anomalies, and regional deposition of hydrothermal dolomite cement. The fluid drive was provided by gravity flow accompanying uplift of foreland thrust belts during the Late Pennsylvanian to Early Permian Ouaehita orogeny.In this study, we use chemical speciation and reaction path calculations, based on quantitative chemical analyses of fluid inclusions, to constrain likely hydrothermal brine compositions and to determine which precipitation mechanisms are consistent with the hydrothermal mineral assemblages observed regionally and locally within each Mississippi Valley-type district in the Ozark region. Deposition of the regional hydrothermal dolomite cement with trace sulfides likely occurred in response to near-isothermal effervescence of CO 2 from basinal brines as they migrated to shallower crustal levels and lower confining pressures. In contrast, our calculations indicate that no one depositional process can reproduce the mineral assemblages and proportions of minerals observed in each Ozark ore district; rather, individual districts require specific depositional mechanisms that reflect the local host-rock composition, structural setting, and hydrology.Both the Northern Arkansas and Tri-State districts are localized by normal faults that likely allowed brines to rise from deeper Cambrian-Ordovician dolostone aquifers into shallower carbonate sequences dominated by limestones. In the Northern Arkansas district, jasperoid preferentially replaced limestones in the mixed dolostone-limestone sedimentary packages. Modeling results indicate that the ore and alteration assemblages in the Tri-State and Northern Arkansas districts resulted from the flow of initially dolomite-saturated brines into cooler limestones. Adjacent to fluid conduits where water/rock ratios were the highest, the limestone was replaced by dolomite. As the fluids moved outward into cooler limestone, jasperoid and sulfide replaced limestone. Isothermal boiling of the ore fluids may have produced open-space filling of hydrothermal dolomite with minor sulfides in breccia and fault zones. Local mixing of the regional brine with locally derived sulfur undoubtedly played a role in the development of sulfide-rich ore runs.Sulfide ores of the Central Missouri district are largely open-space filling of sphalerite plus minor galena in dolostone karst features localized along a broad anticline. Hydrothermal solution collapse during ore deposition was a minor process, indicating dolomite was slightly undersaturated during ore deposition. No silicification and only minor hydrothermal dolomite is present in the ore deposits. The reaction path that best explains the features of the Central Missouri sulfide deposits is the near-isothermal mixing of two dolomite-saturated fluids with different H 2 S and metal contents. Paleokarst features may have allowed the regional brine to rise stratigraphically and mix with locally derived, H 2 S-rich fluids. The Viburnum Trend and Old Lead Belt ores are galena rich with lesser amounts of sphalerite; they replace the most permeable dolostone facies in the Bonneterre Dolomite. Hydrothermal dissolution of host dolostone was concurrent with sulfide deposition, but dolomite deposition occurred episodically between periods of sulfide deposition. The important ore controls in these districts are a variety of sedimentary and geologic features that allowed cross-stratigraphic fluid flow and provided opportunities for fluid mixing. The reaction path which best reproduces the broad features of the Viburnum Trend and Old Lead Belt ores is one in which a dolomite-saturated, lead-rich, zinc- and H 2 S-poor brine mixes with a less saline, H 2 S-rich fluid. The brine became enriched in K, Mg, and Pb and depleted in H 2 S as it flowed through sandstone and redbed aquifers prior to entering the district. This mixing model is consistent with the abundant fluid inclusion and stable isotope evidence for fluid mixing in the districts. Small amounts of cooling associated with the mixing may have contributed to sulfide deposition.

Alabama, Arkansas, Illinois, Indiana, Kansas, Kent↗
USGS1991

Strontium isotopic constraints on the origin of ore-forming fluids of the Viburnum Trend, southeast Missouri

We have measured 87 Sr 86 Sr "> 87Sr86Sr and Rb and Sr concentrations in several minerals, primarily sulfides, spanning the paragenesis of hydrothermal mineralization in the Viburnum Trend in southeast Missouri. Separate measurements were made for fluid inclusions opened by crushing or thermal decrepitation and for the solids. For comparison, measurements were also made on samples of probable local aquifers, the Bonneterre Formation and the Lamotte Sandstone. For some of the samples, concentrations of K, Ca, Cl, Na, and Mg are also reported. In several cases 87 Sr 86 Sr ratios "> 87Sr86Srratios are different (higher) in the solids than in the fluid inclusions. We have investigated the possibility that either type of sample gives spurious results, e.g., that the fluid inclusions are secondary or contaminated by host dolomite, or that Sr in the solids reflects a detrital rather than an authigenic source. Consideration of mass balance, overall solute chemistry, and examination of non-sulfide dissolution residue, however, suggests that both types of sample reflect primary fluid Sr composition. We thus adopt the working hypothesis that Sr isotopic composition in fluids at the time of hydrothermal mineralization was highly variable. The observed results for the Viburnum Trend do not conform well to expected trends for Mississippi Valley-type (MVT) mineralization based primarily on analyses of gangue carbonates, barite, and fluorite. Fluid inclusion Sr in some of the Viburnum Trend samples is more radiogenic than in the host dolomite but only moderately so; in other samples, notably main-stage octahedral galena, fluid inclusion Sr composition is within the range observed for the host dolomite. In contrast, Sr in some of the sulfides is very radiogenic, much more so than previously reported for MVT minerals, and is very radiogenic early in the paragenesis (pyrite, chalcopyrite, sphalerite), less radiogenic during main-stage ore deposition, and again more radiogenic in later paragenetic stages.

Geochimica et Cosmochimica Acta↗
USGS1991

Origin of late dolomite cement by CO2-saturated deep basin brines: evidence from the Ozark region, central United States

Studies of fluid inclusions in regionally extensive late dolomite cement (LDC) throughout the Ozark region show that CO 2 effervescence was widespread during dolomite precipitation. On the basis of quantitative analyses of inclusion fluids, reaction-path modeling shows that LDC with trace amounts of sulfides can be deposited by effervescence of a CO 2 -saturated basin brine as it migrates to shallower levels and lower confining pressures. This precipitation mechanism best explains occurrences of LDC in the Ozark region and may account for LDC found in sedimentary basins worldwide.

Geology↗
USGS1990

Genetic implications of regional and temporal trends in ore fluid geochemistry of Mississippi Valley-type deposits in the Ozark region

Fluids extracted from aqueous fluid inclusions in epigenetic gangue and ore minerals record the migration of huge volumes of highly saline fluids throughout the stratigraphic section of the Ozark region. The extracted fluids share many similarities regionally, but there are significant temporal differences which define two geochemically distinct end-member ore-forming fluids that we refer to as the Viburnum Trend main stage or Viburnum Trend type and the Tri-State type.Viburnum Trend-type fluids are enriched in potassium and are associated only with deposits close to the basal Lamotte Sandstone. The main-stage octahedral galena ore of the Viburnum Trend and much of the Old Lead Belt ore is thought to be derived from this type of ore fluid. Galena deposited by Viburnum Trend-type fluids contains less radiogenic lead than galena deposited by Tri-State-type fluids. Sulfides deposited by Viburnum Trend-type fluids also contain isotopically heavier sulfur and significant amounts of copper, cobalt, nickel, and silver.Tri-State-type fluids have a low potassium content when compared with Viburnum Trend-type fluids and are characteristic of deposits where ore-forming fluids migrated through large volumes of carbonate rock. These fluids are thought to have formed the ore deposits of the Tri-State, Northern Arkansas, and Central Missouri districts, the cubic galena-stage ore of the Viburnum Trend, and the many trace occurrences of sphalerite throughout the Ozark region. Galena deposited by Tri-State-type fluids has more radiogenic lead and the sulfides have isotopically lighter sulfur than sulfides deposited by Viburnum Trend-type fluids. A systematic south to north increase of potassium in the Tri-State-type fluids suggests that they migrated from a southerly source such as the Arkoma basin.Possible explanations for the origins of these two end-member fluids include: (1) a single parent brine evolved into two distinct fluids due to reactions with geochemically distinct aquifers during migration, (2) the two distinct fluids reflect normal fluid evolution within a single source basin of a bittern and of later halite dissolution, and (3) the Viburnum Trend and Tri-State-type brines migrated to southeast Missouri from two different source basins. Our data does not preclude any of these possibilities; however, the geochemical similarity of the Viburnum Trend end-member fluid to a bittern may be accounted for by water-rock modifications of the brine during migration. Other evidence strongly supports a southerly source for the ore-forming brines thus limiting possible sources for the Viburnum Trend-type fluid to the Arkoma and/or Black Warrior basins of the Ouachita foreland trough. Viburnum Trend-type fluid flow was probably funneled northward through basal sandstones within the Reelfoot rift and water-rock modifications occurring there may have resulted in its unique geochemistry.

Economic Geology↗