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D. L. Leach

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

At least 37 records · Page 2Linked to original sources

Genetic characteristics of fluid inclusions in sphalerite from the Silesian-Cracow ores, Poland

Fluid inclusion studies in sphalerite from early-stage Zn-Pb mineralization in the Silesian-Cracow region (southern Poland), yielded homogenization temperatures (Th) from 80 to 158??C. Vertical thermal gradient of the parent fluids was 6 to 10??C, and the ore crystallization temperature ranges varied from <10??C at deep levels to 25??C at shallow levels. The peculiarities of formation of primary and secondary fluid inclusions from organic-matter-bearing water-dominated medium, position of the inclusions in crystals, features of secondary inclusions, the inclusion refilling phenomena, their formation on recrystallization of ores, and Th distribution in single fissure fillings were considered. The ore-forming fluids were liquid-hydrocarbon-bearing aqueous solutions of Na-Ca-Cl type with lower Ca contents in the south and higher Ca contents in the north of the region. The ore-forming fluids had salinities from nul to about 23 weight percent of NaCl equivalent. Three types of fluids were recognized, that mixed during ore precipitation: a) ascending fluids of low-to-moderate salinity and high, b) formation brines of high salinity and moderate Th, and c) descending waters of low salinity and low-to-moderate Th.

Prace - Panstwowego Instytutu Geologicznego↗

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↗

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↗

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↗

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↗

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↗

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↗

Constraints from fluid inclusions on sulfide precipitation mechanisms and ore fluid migration in the Viburnum Trend lead district, Missouri

Measurements on fluid inclusions in hydrothermal dolomite cements place constraints on sulfide precipitation mechanisms and on the thermal-hydrologic processes which formed the Viburnum Trend Mississippi Valley-type lead district. Homogenization temperatures and freezing point depressions were determined for fluid inclusions in Bonneterre Dolomite-hosted dolomite cements in mine samples, as well as drill core from up to 13 km outside of the district. A well-defined cathodoluminescent zonation distinguishes dolomite growth zones in the Vi-burnurn Trend as older or younger than main-stage mineralization (octahedral galena) and facilitates correlation with other dolomites outside the Viburnum Trend.Homogenization temperatures and salinities in samples from mines are not systematically different from those of samples outside of the district. Medians of homogenization temperature distributions differ by not more than 25 degrees C, so that a temperature gradient, if present, should not have exceeded approximately 25 degrees C within the study area. These observations are interpreted to indicate that the Viburnum Trend was not strongly thermally anomalous with respect to surrounding country rock and that fluid flow occurred on a broad scale through not only the Lamotte Sandstone but through the overlying Cambrian carbonates as well.The absence of a significant, recognizable decrease in temperature either vertically within the section or east-west across the district, coupled with the minor amount of silica in the district, argues against cooling as a primary cause of sulfide precipitation. Fluids whose primary aquifer was the Lamotte Sandstone, predominantly a quartz arenite, should have been in equilibrium with quartz. Quartz in the Viburnum Trend occurs as a minor, drusy, vug-lining phase, but the district lacks the intense silicification found in other Mississippi Valley-type districts such as Tri-State (Oklahoma, Kansas, Missouri). Quartz solubility is strongly temperature dependent and, under equilibrium conditions, a decrease of 10 degrees C or more should have precipitated at least as many moles of silica as galena (assuming a galena solubility of between 1 and 10 ppm). Clearly this is not the case, as galena is far more abundant than quartz in the Viburnum Trend.Ice final-melting temperatures (T m ) in fluid inclusions generally range from -14 degrees to -27 degrees C for primary dolomite-hosted inclusions. Using these T m values and cation ratios for the inclusion fluids, absolute concentrations for the individual cations and chloride were calculated using the thermochemical model of Spencer et al. (1990). The corresponding high but variable salinities, 3.9 to 5.9 chloride molality, are evidence for the presence of more than one distinct fluid during mineralization.In a reduced sulfur mineralization model with Pb carried as chloride complexes, dilution is also a possible sulfide precipitation mechanism. The difference in Pb solubility (for an equal quantity of reduced sulfur) in the extremes of the chloride concentration range, 3.9 vs. 5.9 molal, reaches 1 ppm only for pH values below approximately 4.5. Accepting 1 ppm as a minimum metal concentration for a viable ore-forming fluid, dilution only appears capable of precipitating sulfides in a fluid with pH near the lower limit of values considered geologically reasonable or attainable.Dolomite cements hosting warm (approximately 105 degrees -125 degrees C) saline fluid inclusions are ubiquitous in the porous dolomitic facies of the Bonneterre Dolomite. Based on stratigraphic reconstructions, however, it is unlikely that the Bonneterre was buried deeper than 1.5 km. The distribution of warm inclusions beyond the Viburnum Trend district implies that fluid migration was regional in scale. Fluid inclusion temperatures inconsistent with typical basement heat-flow-controlled geothermal gradients (25 degrees -35 degrees C/km) may be explained by long-distance migration of warm, basin-derived brines. Elevated temperatures observed in fluid inclusions at shallow stratigraphic depths are consistent with a gravity flow hydrologic system characterized by rapid flow rates and the capacity for advective heat transport.

Economic Geology↗