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Speleology in Kazakhstan

Shakalov on 04 Jul, 2018
Hello everyone!   I pleased to invite you to the official site of Central Asian Karstic-Speleological commission ("Kaspeko")   There, we regularly publish reports about our expeditions, articles and reports on speleotopics, lecture course for instructors, photos etc. ...

New publications on hypogene speleogenesis

Klimchouk on 26 Mar, 2012
Dear Colleagues, This is to draw your attention to several recent publications added to KarstBase, relevant to hypogenic karst/speleogenesis: Corrosion of limestone tablets in sulfidic ground-water: measurements and speleogenetic implications Galdenzi,

The deepest terrestrial animal

Klimchouk on 23 Feb, 2012
A recent publication of Spanish researchers describes the biology of Krubera Cave, including the deepest terrestrial animal ever found: Jordana, Rafael; Baquero, Enrique; Reboleira, Sofía and Sendra, Alberto. ...

Caves - landscapes without light

akop on 05 Feb, 2012
Exhibition dedicated to caves is taking place in the Vienna Natural History Museum   The exhibition at the Natural History Museum presents the surprising variety of caves and cave formations such as stalactites and various crystals. ...

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That albedo is the ratio of reflected radiation to total radiation on a natural surface [16].?

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Featured articles from Cave & Karst Science Journals
Chemistry and Karst, White, William B.
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Karst environment, Culver D.C.
Mushroom Speleothems: Stromatolites That Formed in the Absence of Phototrophs, Bontognali, Tomaso R.R.; D’Angeli Ilenia M.; Tisato, Nicola; Vasconcelos, Crisogono; Bernasconi, Stefano M.; Gonzales, Esteban R. G.; De Waele, Jo
Calculating flux to predict future cave radon concentrations, Rowberry, Matt; Marti, Xavi; Frontera, Carlos; Van De Wiel, Marco; Briestensky, Milos
Microbial mediation of complex subterranean mineral structures, Tirato, Nicola; Torriano, Stefano F.F;, Monteux, Sylvain; Sauro, Francesco; De Waele, Jo; Lavagna, Maria Luisa; D’Angeli, Ilenia Maria; Chailloux, Daniel; Renda, Michel; Eglinton, Timothy I.; Bontognali, Tomaso Renzo Rezio
Evidence of a plate-wide tectonic pressure pulse provided by extensometric monitoring in the Balkan Mountains (Bulgaria), Briestensky, Milos; Rowberry, Matt; Stemberk, Josef; Stefanov, Petar; Vozar, Jozef; Sebela, Stanka; Petro, Lubomir; Bella, Pavel; Gaal, Ludovit; Ormukov, Cholponbek;
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Your search for galena (Keyword) returned 19 results for the whole karstbase:
Showing 1 to 15 of 19
Stalactites and Helictites of Marcasite, Galena, and Sphalerite in Illinois and Wisconsin, 1979, Peck, Stewart B

The Coxco Deposit; a Proterozoic mississippi valley-type deposit in the McArthur River District, Northern Territory, Australia, 1983, Walker R. N. , Gulson B. , Smith J. ,
Strata-bound dolomite-hosted lead-zinc deposit. Crusts of colloform sphalerite, galena, pyrite, and marcasite (stage I mineralization) were deposited on the surfaces of the karst-produced solution cavities. Reduced sulfur was produced by sulfate-reducing bacteria within the karst system. A second stage of mineralization consisting of coarsely crystalline sphalerite, galena, pyrite, and marcasite occurs in veins and as the matrix for dolomite breccias.--Modified journal abstract

The lead-zinc ore deposits of the Siding-Gudan mineral subdistrict Guangxi are part of the large Nanling district of South China, and hosted in Devonian carbonate rocks. The ore bodies occur significantly along main faults and fault zones, and concentrate up to 300 meters above the Cambrian/Devonian unconformity. Connected with hydrothermal karst, size and volume of the ore bodies increase in proximity to this unconformity. Moving from the unaffected host rocks to the center of the ore bodies, four zones can be discriminated by the mineral assemblage (pyrite, sphalerite, galena) as well as by the degree of ordering, Ca/Mg, and Fe/Mn ratios of different dolomites. Homogenization temperatures range from 80-100-degrees-C (Presqu'ile dolomite) to 230-260-degrees-C (massive sphalerite). The sulfides reveal delta-S-34 = -20 to parts per thousand, and fluid inclusions display a salinity of 5-12 wt % equivalent NaCl. The diagenetic and hydrothermal history is similar to that of classic Mississippi Valley Type (MVT) sulfide mineral deposits as, for example, Pine Point in Canada. Mineralization and remobilization of the sulfides took place during a wide time span from late Paleozoic through Mesozoic. Both processes are considered as an interaction of saline basinal brines ascended from the adjoining dewatering trough, and magmatic-hydrothermal fluids of several magmatic-tectonic events

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 Ouachita 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 CO2 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 H2S and metal contents. Paleokarst features may have allowed the regional brine to rise stratigraphically and mix with locally derived, H2S-rich fluids

Occurrence and significance of stalactites within the epithermal deposits at Creede, Colorado, 1996, Campbell Wr, Barton Pb,
In addition to the common and abundant features in karst terranes, stalactites involving a wide variety of minerals have also been found in other settings, including epigenetic mineral deposits, bur these are almost always associated with supergene stages. Here we describe a different mode of occurrence from the Creede epithermal ore deposits, in Colorado, wherein stalactites of silica, sphalerite, galena, or pyrite formed in a vapor-dominated setting, below the paleo-water table, and except possibly for pyrite, as part of the hypogene mineralization. Axial cavities may, or may not, be present. No stalagmites have been recognized. The stalactites are small, from a few millimeters to a few centimeters long and a few millimeters in outer diameter. They represent only a small fraction of one percent of the total mineralization, and are covered by later crystals. Their growth orientation usually is unobservable; however, the parallel arrangement of all stalactites in a given specimen, consistency with indicators of gravitational settling, and the common presence of axial structures make the stalactitic interpretation almost unavoidable. In contrast with common carbonate stalactites, the growth mechanism for th sulfide and silica stalactites requires extensive evaporation. Stalactitic forms have also been reported from other deposits, mostly epithermal or Mississippi Valley-type occurrences, but we caution that stalactite-like features can form by alternative processes

Origin of iron-rich Mississippi Valley-type deposits, 2001, Marie James St, Kesler Stephen E. , Allen Cameron R. ,
The abundance of iron in Mississippi Valley-type lead-zinc deposits and districts varies greatly; some deposits contain large amounts and others are almost free of iron. Iron in Mississippi Valley-type deposits is largely paragenetically early pyrite or marcasite that was replaced by sphalerite and galena, often in the central part of the deposit or district. Sedimentary exhalative and Irish-type base metal deposits, which also form from basinal brines, have similar variations in iron content. Calculated metal contents of brines in equilibrium with galena, sphalerite, and pyrite show that iron is significantly more abundant than lead and zinc in high-temperature (>200 {degrees}C), relatively acid brines with low sulfur contents, whereas zinc dominates under most other conditions, including brines with high temperatures and high sulfur contents. These results suggest that iron-rich Mississippi Valley-type deposits form from brines expelled from the deepest, hottest parts of sedimentary basins

Results from the Big Spring basin water quality monitoring and demonstration projects, Iowa, USA, 2001, Rowden R. D. , Liu H. B. , Libra R. D. ,
Agricultural practices, hydrology, and water quality of the 267-km(2) Big Spring groundwater drainage basin in Clayton County, Iowa, have been monitored since 1981. Land use is agricultural; nitrate-nitrogen (-N) and herbicides are the resulting contaminants in groundwater and surface water. Ordovician Galena Group carbonate rocks comprise the main aquifer in the basin. Recharge to this karstic aquifer is by infiltration, augmented by sinkhole-captured runoff. Groundwater is discharged at Big Spring, where quantity and quality of the discharge are monitored. Monitoring has shown a threefold increase in groundwater nitrate-N concentrations from the 1960s to the early 1980s. The nitrate-N discharged from the basin typically is equivalent to over one-third of the nitrogen fertilizer applied, with larger losses during wetter years. Atrazine is present in groundwater all year; however, contaminant concentrations in the groundwater respond directly to recharge events, and unique chemical signatures of infiltration versus runoff recharge are detectable in the discharge from Big Spring. Education and demonstration efforts have reduced nitrogen fertilizer application rates by one-third since 1981. Relating declines in nitrate and pesticide concentrations to inputs of nitrogen fertilizer and pesticides at Big Spring is problematic. Annual recharge has varied five-fold during monitoring, overshadowing any water-quality improvements resulting from incrementally decreased inputs

Mineralogy and geochemistry of trace elements in bauxites: the Devonian Schugorsk deposit, Russia, 2001, Mordberg L. E. , Stanley C. J. , Germann K. ,
Processes of mineral alteration involving the mobilization and deposition of more than 30 chemical elements during bauxite formation and epigenesis have been studied on specimens from the Devonian Schugorsk bauxite deposit, Timan, Russia. Chemical analyses of the minerals were obtained by electron microprobe and element distribution in the minerals was studied by element mapping. Interpretation of these data also utilized high-resolution BSE and SE images. The main rock-forming minerals of the Vendian parent rock are calcite, dolomite, feldspar, aegirine, riebeckite, mica, chlorite and quartz; accessory minerals are pyrite, galena, apatite, ilmenite, monazite, xenotime, zircon, columbite, pyrochlore, chromite, bastnaesite and some others. Typically, the grain-size of the accessory minerals in both parent rock and bauxite is from 1 to 40 {micro}m. However, even within these rather small grains, the processes of crystal growth and alteration during weathering can be determined from the zonal distribution of the elements. The most widespread processes observed are: (1) Decomposition of Ti-bearing minerals such as ilmenite, aegirine and riebeckite with the formation of leucoxene', which is the main concentrator of Nb, Cr, V and W. Crystal growth can be traced from the zonal distribution of Nb (up to 16 wt.%). Vein-like leucoxene' is also observed in association with organics. (2) Weathering of columbite and pyrochlore: the source of Nb in leucoxene' is now strongly weathered columbite, while the alteration of pyrochlore is expressed in the growth of plumbopyrochlore rims around Ca-rich cores. (3) Dissolution of sulphide minerals and apatite and the formation of crandallite group minerals: crandallite' crystals of up to 40 {micro}m size show a very clear zonation. From the core to the rim of a crystal, the following sequence of elements is observed: Ca [->] Ba [->] Ce [->] Pb [->] Sr [->] Nd. Sulphur also shows a zoned but more complicated distribution, while the distribution of Fe is rather variable. A possible source of REE is bastnaesite from the parent rock. More than twelve crandallite type cells can be identified in a single crandallite' grain. (4) Alteration of stoichiometric zircon and xenotime with the formation of metamict solid solution of zircon and xenotime: altered zircon rims also bear large amounts of Sc (up to 3.5 wt.%), Fe, Ca and Al in the form of as yet unidentified inclusions of 1-2 {micro}m. Monazite seems to be the least altered mineral of the profile. In the parent rock, an unknown mineral of the composition (wt.%): ThO2 - 54.8; FeO - 14.6; Y2O5 -2.3; CaO - 2.0; REE - 1.8; SiO2 - 12.2; P2O5 - 2.8; total - 94.2 (average from ten analyses) was determined. In bauxite, another mineral was found, which has the composition (wt.%): ThO2 - 24.9; FeO - 20.5; Y2O5 - 6.7; CaO - 2.0; ZrO - 17.6; SiO2 - 8.8; P2O5 - 5.4; total - 89.3 (F was not analysed; average from nine analyses). Presumably, the second mineral is the result of weathering of the first one. Although the Th content is very high, the mineral is almost free of Pb. However, intergrowths of galena and pyrite are observed around the partially decomposed crystals of the mineral. Another generation of galena is enriched in chalcophile elements such as Cu, Cd, Bi etc., and is related to epigenetic alteration of the profile, as are secondary apatite and muscovite

Formation of Willemite in Hydrothermal Environments, 2003, Brugger J, Mcphail Dc, Wallace M, Waters J,
Willemite (zinc silicate) is the main zinc mineral in some carbonate-hosted ore deposits (e.g., Franklin, New Jersey; Vazante, Brazil; Beltana, South Australia; Kabwe, Zambia). Recent interest in these unconventional zinc deposits has increased because of high zinc grades that exceed 40 wt percent, relatively low environmental impact of ore processing owing to the lack of acid-generating sulfides in the waste, and advances in ore processing technologies. In the past, most metallogenic studies proposed formation of willemite deposits by supergene or hypogene alteration of preexisting sulfide deposits. However, recent data on the Vazante, Beltana, and Kabwe deposits indicate willemite crystallization at temperatures in excess of 150{degrees}C, raising the possibility of primary precipitation from hydrothermal fluids. We use numerical geochemical modeling to examine the formation of willemite under hydrothermal conditions. Activity-activity diagrams reveal that, in the presence of dissolved sulfur and quartz, willemite instead of sphalerite will precipitate under oxidizing (e.g., hematite-stable, sulfate-predominant) and alkaline (pH higher than K feldspar-muscovite-quartz) conditions. Willemite also becomes more stable, relative to sphalerite, at high temperature, and willemite can coexist with magnetite at 300{degrees}C. The stabilities and solubilities of sphalerite, willemite, smithsonite, hydrozincite, and zincite were calculated for wide ranges of temperature (25{degrees}-300{degrees}C), chloride concentration, dissolved sulfur and carbon concentrations, pH, quartz saturation, and oxidation potential. Plots of the solubility of the different minerals as a function of two variables (e.g., temperature and redox state; pH and redox state) allow us to predict the effects of changing chemical conditions, which in turn permits an estimate of the efficiency of particular precipitation processes. Cooling is an effective process for precipitating sphalerite but not willemite, whereas pH increase (e.g., by acidic fluids reacting with carbonates) is effective for precipitating willemite but not sphalerite. Dynamic geochemical models that simulate physicochemical processes are used to understand the formation of the Beltana willemite deposit in the Adelaide geosyncline of South Australia. This small, high grade deposit (850,000 t at 36% Zn) is hosted in dolomite of the Cambrian Ajax Limestone, next to a tectonic contact with the diapiric, halite-bearing clastic sediments of the Callanna Group. The orebody is associated with hematite alteration and is characterized by the total absence of sulfides; willemite is the only zinc ore mineral, and the arsenate hedyphane (Ca2Pb3[AsO4]3Cl) is the main lead mineral. The model results show that willemite will precipitate in response to water-rock interaction and fluid mixing processes at temperatures above 120{degrees}C. The presence of arsenate in the hydrothermal fluid is likely to have been important at Beltana; in arsenate-absent models sulfate is reduced to sulfide by the precipitation of ferrous iron as hematite, resulting in the precipitation of sphalerite and galena. In contrast, in models including arsenate the reduction of sulfate to sulfide is inhibited and willemite is predicted to precipitate

Carbonate-Hosted Zn-Pb Deposits in Upper Silesia, Poland: Origin and Evolution of Mineralizing Fluids and Constraints on Genetic Models, 2003, Heijlen Wouter, Muchez Philippe, Banks David A. , Schneider Jens, Kucha Henryk, Keppens Eddy,
Microthermometric and crush-leach analyses of fluid inclusions in ore and gangue minerals of the Upper Silesian Zn-Pb deposits, Poland, along with first results of Rb-Sr geochronology on sulfides, provide important constraints on the paleohydrogeologic and metallogenetic models for the origin of these ores. The analyzed samples comprise two generations of dolomite, two generations of sphalerite, galena, and late calcite. The two dolomite generations and the late calcite were also analyzed for their oxygen and carbon isotope compositions, allowing a characterization of the mineralizing fluids. The ore-forming fluids represent highly saline (20-23 wt % CaCl2 equiv) Na-Ca-Cl brines, episodically introduced into the Triassic host carbonates. They had an oxygen isotope composition of ~0 per mil V-SMOW. Their Na-Cl-Br content (molar Na/Br and Cl/Br ratios between 99 and 337 and between 248 and 560, respectively) suggests that they originated by evaporation of seawater, which most likely occurred in the Permian-Triassic. The relative concentrations of potassium (molar K/Cl between 0.0147 and 0.0746) and lithium (molar Li/Cl between 0.0004 and 0.0031) further indicate that the fluids significantly interacted with siliciclastic rocks. The ionic and calculated oxygen isotope compositions of the fluids indicate that they were more evolved than present-day brines in the Upper Silesian coal basin, and the present-day brines show more extensive mixing with low-salinity fluids. The first results of direct Rb-Sr dating of ore-stage sulfides yield an isochron model age of 135 {} 4 Ma for the mineralizing event. This is consistent with hydrothermal activity and ore formation in Upper Silesia occurring in response to Early Cretaceous crustal extension preceding the opening of the northern Atlantic Ocean. The data presented support a model in which bittern brines migrated down into the deep subsurface and evolved into mineralizing fluids owing to extensive water-rock interaction. They were episodically expelled along deeply penetrating faults during the Early Cretaceous to form Zn-Pb deposits in the overlying Mesozoic carbonate rocks

The Padaeng Supergene Nonsulfide Zinc Deposit, Mae Sod, Thailand, 2003, Reynolds Neal A. , Chisnall Tony W. , Kaewsang Kriangsak, Keesaneyabutr Chanan, Taksavasu Taksorn,
The Padaeng deposit near Mae Sod in western Thailand was the first supergene nonsulfide zinc deposit in the world to be developed as a large modern mining operation. The mine and associated zinc smelter, operated by Padaeng Industry Public Company Ltd. since 1984, went into production with reserves of 4.59 Mt at a grade of 28.9 percent zinc with a 10 percent zinc cutoff. Current resources are 5.14 Mt at a grade of 12.0 percent zinc with a 3 percent zinc cutoff. The Padaeng deposit is hosted by a mixed carbonate-clastic sequence of Middle Jurassic age. The deposit occurs in the hanging wall of the Padaeng fault, a major northwest-trending structure that was active through Cretaceous and Tertiary tectonism and uplift. Nonsulfide zinc ore comprises dominant hemimorphite with minor smithsonite and hydrozincite. Strata-bound ore zones occur within a northwest-dipping, deeply weathered, dolomitic sandstone; steeply dipping and irregular karstic zones in underlying massive, silty dolomite are controlled by north-trending fracture zones. Sulfide zinc-lead mineralization of Mississippi Valley type occured extensively in the vicinity of the Padaeng mine, most notably the small resources at Pha De and Hua Lon. Mineral deposits are typically sphalerite rich with minor galena and pyrite, forming small-scale open-space fillings, veins, and replacements within hydrothermal dolomite. Mineralization is dominantly strata bound within a horizon of intense hydrothermal dolomitization that forms the stratigraphic hanging wall to the nonsulfide ore zones at Padaeng. The only significant sulfide at the Padaeng mine is within this unit. Only trace sulfide occurs peripheral to, or down dip of, strata-bound or steeply dipping, nonsulfide orebodies. Sulfide mineralization is believed to have accompanied Cretaceous uplift and deformation, related to the onset of oblique subduction beneath the western margin of the Shan-Thai terrane. The nonsulfide deposit is believed to have formed when a substantial body of sulfide ore was uplifted on the margin of the Mae Sod Tertiary intermontane basin, commencing in the middle to late Miocene. Zinc-bearing acidic supergene fluids, generated by oxidation of the precursor sulfide body, reacted with carbonate in the underlying stratigraphic section to precipitate hemimorphite and smithsonite. Fluids were channeled by permeable dolomitic sandstones and by steep fracture and fault zones. Acidic fluids promoted deep weathering and karst formation, allowing mineralization to extend down dip in sandstone units for at least 150 m and vertically for a similar distance in steep structural zones. Transport of zinc out of the precursor sulfide body was facilitated by a falling water table, owing to uplift of the Padaeng fault block and a change from wet tropical to monsoonal or semiarid climatic conditions. There is no evidence for significant in situ replacement of sulfide deposits, and the leached remnants of the precursor sulfide body have been removed by erosion. The supergene process of dissolution and reprecipitation of zinc in the host rocks increased zinc grades and separation of zinc from lead, producing an economically attractive deposit. Successful exploration for this type of deposit requires a good understanding of the controls on primary sulfide mineralization and a good knowledge of local neotectonism, uplift history, hydrogeology, climatic evolution, and weathering history

Geology and Geochemistry of the Reocin Zinc-Lead Deposit, Basque-Cantabrian Basin, Northern Spain, 2003, Velasco Francisco, Herrero Jose Miguel, Yusta Inaki, Alonso Jose Antonio, Seebold Ignacio, Leach David,
The Reocin Zn-Pb deposit, 30 km southwest of Santander, Spain, occurs within Lower Cretaceous dolomitized Urgonian limestones on the southern flank of the Santillana syncline. The Reocin deposit is one of the largest known strata-bound, carbonate-hosted, zinc-lead deposits in Europe. The total metal endowment of the deposit, including past production and remaining reserves, is 62 Mt of ore grading 8.7 percent Zn and 1.0 percent Pb. The epigenetic mineralization consists of sphalerite and galena, with lesser marcasite and trace pyrite with dolomite as gangue. Microprobe analyses of different generations of dolomite revealed nonstoichiometric compositions with various amounts of iron (up to 14 mol % of FeCO3). Replacement of host dolomite, open-space filling of fractures, and cementation of breccias derived from dissolution collapse are the principal types of ore occurrence. Detailed cross-section mapping indicates a stratigraphic and structural control on the deposit. A stratiform morphology is present in the western part of the orebody (Capa Sur), whereas mineralization in the eastern part is highly discordant but strata bound (Barrendera). Stratigraphic studies demonstrate that synsedimentary tectonic activity, related to the rifting of the North Atlantic (Bay of Biscay), was responsible for variation in sedimentation, presence of unconformities (including paleokarsts), local platform emergence and dolomitization along the N60 fault trend. In the Reocin area, two stages of dolomitization are recognized. The first stage is a pervasive dolomitization of the limestone country rocks that was controlled by faulting and locally affected the upper part of the Aptian and the complete Albian sequence. The second dolomitization event occurred after erosion and was controlled by karstic cavities. This later dolomitization was accompanied by ore deposition and, locally, filling of dolomite sands and clastic sediments in karstic cavities. The circulation of hydrothermal fluids responsible for sulfide deposition and the infilling of karst cavities were broadly contemporaneous, indicating a post-Albian age. Vitrinite reflectance data are consistent with previously measured fluid inclusion temperatures and indicate temperatures of ore deposition that were less than 100{degrees}C. Carbon and oxygen isotopic data from samples of regional limestone, host-rock dolostone and ore-stage dolomite suggest an early hydrothermal alteration of limestone to dolostone. This initial dolomitization was followed by a second period of dolomite formation produced by the mixing of basinal metal-rich fluids with local modified seawater. Both dolomitization events occurred under similar conditions from fluids exhibiting characteristics of basinal brines. The{delta} 34S values of sulfides are between -1.8 and .5 per mil, which is consistent with thermochemical sulfate reduction involving organic matter as the main source of reduced sulfur. Galena lead isotope compositions are among the most radiogenic values reported for Zn-Pb occurrences in Europe, and they are distinct from values reported for galena from other Basque-Cantabrian deposits. This suggests that a significant part of the lead was scavenged from the local underlying Asturian sediments. The stratigraphic and structural setting, timing of epigenetic mineralization, mineralogy, and isotopic geochemistry of sulfide and gangue minerals of the Reocin deposit are consistent with the features of most of Mississippi Valley-type ore deposits

Basin fluid flow, base-metal sulphide mineralization and the development of dolomite petroleum reservoirs, 2004, Gregg Jay M. ,
Saline basinal fluids, at temperatures from 60 to 250 {degrees}C, have affected almost every sedimentary basin in the world including rocks from Palaeoproterozoic to Cenozoic age. These fluids commonly precipitate base-metal sulphides (pyrite, sphalerite, galena, etc.) and associated minerals (barite, fluorite, calcite, dolomite, etc.) ranging in volume from trace amounts to large economic ore deposits. Such deposits are commonly referred to as Mississippi Valley-type (MVT) after the large Palaeozoic deposits of this kind found in the Mississippi Valley of North America. They are primarily hosted by platform carbonates, typically dolomite, and are usually associated with hydrocarbons. Dolomites not affected by mineralizing fluids commonly display micron- to decimicron-size planar textures, and have well-developed micro- and mesoporosity networks dominated by intercrystal and vug porosity. However, these and other carbonate rocks affected by basinal fluids may undergo massive geochemical and textural alteration. This occurs even when the affected rocks are distal from the main loci of sulphide mineralization. Alteration includes: dolomitization of limestone; neomorphic recrystallization of existing dolomite; and precipitation at intervals of large volumes of open-space-filling dolomite, calcite and quartz cements alternating with dissolution. Dolomitization of limestone and/or neomorphic recrystallization of dolomite, at elevated temperatures, commonly results in centimicron and larger size crystals, and development of nonplanar textures that increase pore-throat tortuosity. Open-space-filling dolomite, calcite and quartz cementation causes a dramatic reduction of porosity and blockage of pore throats. Periods of carbonate dissolution, proximal to intense sulphide mineralization, result in the development of large-scale macroporosity such as breccias that are commonly superimposed on karst and tectonic fractures. Exposure to mineralizing basinal fluids substantially alters porosity and permeability distribution, and thus the potential reservoir properties of the dolomite. The resulting reservoir may have little resemblance to its precursor. Understanding the epigenetic history of a dolomite is critical, therefore, as this will ultimately affect its development strategy and production history

Isotope geochemistry of the mafic dikes from the Vazante nonsulfide zinc deposit, Brazil, 2007, Babinski M. , Monteiro L. V. S. , Fetter A. H. , Bettencourt J. S. , Oliveir T. F.
The Vazante Group, located in the northwestern part of Minas Gerais, hosts the most important zinc mine in Brazil, the Vazante Mine, which represents a major known example of a hypogene nonsulfide zinc deposit. The main zinc ore is represented by willemite and differs substantially from other deposits of the Vazante-Paracatu region, which are sulfide-dominated zinc-lead ore. The age of the Vazante Group and the hosted mineralization is disputable. Metamorphosed mafic dikes (metabasites) that cut the metasedimentary sequence and are affected by hydrothermal processes recently were found and may shed light on the geochronology of this important geological unit. Zircon crystals recovered from the metabasites are xenocrystic grains that yield U?Pb conventional ages ranging from 2.1 to 2.4 Ga, so the basement of the Vazante Group is Paleoproterozoic or has metasedimentary rocks whose source area was Paleoproterozoic. Pb isotopes determined for titanite separated from the metabasites have common, nonradiogenic Pb compositions, which prevents determination of their crystallization age. However, the Pb signatures observed for the titanite crystals are in agreement with those determined for galena from the carbonate-hosted Zn?Pb deposits hosted by the Vazante Group, including galena from minor sulfide ore bodies of the Vazante deposit. These similarities suggest that the metalliferous fluids that affected the metabasites may have been those responsible for galena formation, which could imply a similar lead source for both nonsulfide and sulfide zinc deposits in the Vazante?Paracatu district. This common source could be related to deep-seated, basin-derived, metalliferous fluids associated with a long-lived hydrothermal system related to diagenesis and deformation of the Vazante Group during the Neoproterozoic.

Geochemical/isotopic evolution of Pb-Zn deposits in the Central and Eastern Taurides, Turkey, 2011, Hanilci N. , Ozturk H.

The Central and Eastern Taurides contain numerous carbonate-hosted Pb-Zn deposits, mainly in Devonian and Permian dolomitized reefal-stramatolitic limestones, and in massive Jurassic limestones. We present and compare new fluid inclusion and isotopic data from these ore deposits, and propose for the first time a Mississippi Valley-type (MVT) mode of origin for them. Fluid inclusion studies reveal that the ore fluids were highly saline (13-26% NaCl equiv.), chloride-rich (CaCl2) brines, and have average homogenization temperatures of 112°C, 174.5°C, and 211°C for the Celal Dag, Delikkaya, and Ayrakl deposits, respectively. Furthermore, the ?34S values of carbonate-hosted Pb-Zn deposits in the Central and Eastern Taurides vary between -5.4‰ and +13.70‰. This indicates a possible source of sulphur from both organic compounds and crustal materials. In contrast, stable sulphur isotope data (average ?34S -0.15‰) for the Cadrkaya deposit, which is related to a late Eocene-Oligocene (?) granodioritic intrusion, indicates a magmatic source. The lead isotope ratios of galena for all investigated deposits are heterogeneous. In particular, with the exception of the Sucat district, all deposits in the Eastern (Delikkaya, Ayrakl, Denizovas, Cadrkaya) and Central (Katranbasi, Kucuksu) Taurides have high radiogenic lead isotope values (206Pb/204Pb between 19.058 and 18.622; 207Pb/204Pb between 16.058 and 15.568; and 208Pb/204Pb between 39.869 and 38.748), typical of the upper continental crust and orogenic belts. Fluid inclusion, stable sulphur, and radiogenic lead isotope studies indicate that carbonate-hosted metal deposits in the Eastern (except for the Cadrkaya deposit) and the Central Taurides are similar to MVT Pb-Zn deposits described elsewhere. The primary MVT deposits are associated with the Late Cretaceous-Palaeocene closure of the Tethyan Ocean, and formed during the transition from an extensional to a compressional regime. Palaeogene nappes that typically limit the exposure of ore bodies indicate a pre-Palaeocene age of ore formation. Host rock lithology, ore mineralogy, fluid inclusion, and sulphur + lead isotope data indicate that the metals were most probably leached from a crustal source such as clastic rocks or a crystalline massif, and transported by chloride-rich hydrothermal solutions to the site of deposition. Localization of the ore deposits on autochthonous basement highs indicates long-term basinal fluid migration, characteristic of MVT depositional processes. The primary MVT ores were oxidized in the Miocene, resulting in deposition of Zn-carbonate and Pb-sulphate-carbonate during karstification. The ores underwent multiple cycles of oxidation and, in places, were re-deposited to form clastic deposits. Modified deposits resemble the 'wall-rock replacement' and the 'residual and karst fill' of non-sulphide zinc deposits and are predominantly composed of smithsonite

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