Community news

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. ...

Did you know?

That single outlet is a stream cutting through a divide (tributary basin) or outflow to the sea (major basin) [16].?

Checkout all 2699 terms in the KarstBase Glossary of Karst and Cave Terms

What is Karstbase?

Search KARSTBASE:

keyword
author

Browse Speleogenesis Issues:

KarstBase a bibliography database in karst and cave science.

Featured articles from Cave & Karst Science Journals
Chemistry and Karst, White, William B.
See all featured articles
Featured articles from other Geoscience Journals
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;
See all featured articles from other geoscience journals

Search in KarstBase

Your search for barite (Keyword) returned 25 results for the whole karstbase:
Showing 1 to 15 of 25
Strontium geochemical evidence for the origin of the barite deposits from Sardinia, Italy, 1984, Barbieri M, Masi U, Tolomeo L,
Sr content of 137 samples of barite, 81 samples of fluorite, and 65 samples of calcite from 27 post-Cambrian karst and hydrothermal deposits. Karst calcites have an average Sr content of 26 ppm, quite similar to that of the hydrothermal calcites. Hydrothermal fluorites show an average content of 56 ppm. Forty-five percent of the karst barites have an Sr content over 6,000 ppm, while as much as 83.8 percent of the hydrothermal barites contain more than 6,000 ppm Sr. The Sr isotope composition of the Cambrian stratiform barites (0.70867 or - 3) is similar to that of Cambrian seawater, suggesting that the bulk of the Sr was provided by this source. The Sr isotope ratios of the karst barite (average 87 Sr/ 86 Sr = 0.70947 or - 1) indicate that Sr was not only derived by recycling of the stratiform barite but was also provided by the noncarbonate fraction of the Cambrian wall rocks. The Sr isotope composition of the hydrothermal barites ranges from 0.70990 or - 4 to 0.71837 or - 4, suggesting that the Sr derived mainly from a high 87 Sr/ 86 Sr ratio source.--Modified journal abstract

Geologic and geochemical controls of mineralization in the southeast Missouri barite district, 1987, Kaiser C. J. , Kelly W. C. , Wagner R. J. , Shanks W. C.

Oxygen, sulfur, and strontium isotope and fluid inclusion studies of barite deposits from the Iglesiente-Sulcis mining district, Southwestern Sardinia, Italy, 1989, Cortecci G, Fontes Jc, Maiorani A, Perna G, Pintus E, Turi B,

LATE TO POSTHERCYNIAN HYDROTHERMAL ACTIVITY AND MINERALIZATION IN SOUTHWEST SARDINIA (ITALY), 1992, Boni M, Iannace A, Koppel V, Fruhgreen G, Hansmann W,
Several kinds of base metal deposits occur in the lower Paleozoic of southwest Sardinia (Iglesiente-Sulcis mineral district). This paper deals with those deposits which are generally referred to as Permo-Triassic, because they accompany and postdate the Hercynian orogeny and are related to magmatic activity. A large number of previously published geochemical data, integrated with additional new data (Sr, Pb, O, C, and S isotopes), are reviewed and discussed in the frame of the late to post-Hercynian geologic evolution of southwest Sardinia. According to geological and mineralogical characteristics, three types of deposits can be distinguished: (1) skarn ores related to late Hercynian leucogranitic intrusions, (2) high-temperature veins, and (3) low-temperature veins and karst filling. Pervasive epigenetic dolomitization phenomena are geochemically related to the low-temperature deposits. Sr and Pb isotopes of the first and second types (0.7097-0.7140 Sr-87/Sr-86; 17.97-18.29 Pb-206/Pb-204; 38.11-38.45 Pb-208/Pb-204) are distinctly more radiogenic than those of the third type (0.7094-0.7115 Sr-87/Sr-86; 17.86-18.05 Pb-206/Pb-204; 37.95-38.19 Pb-208/Pb-204) which, in turn, are closer to Paleozoic ores and carbonates. Fluid inclusion data indicate that the fluids responsible for mineralization of the first and second types of deposits were hot and dilute (T(h)= 370-degrees-140-degrees-C; <5 wt % NaCl equiv). In contrast, relatively colder and very saline fluids (T(h)= 140-degrees-70-degrees-C; >20 wt % NaCl equiv) were responsible for the third type of mineralization, as well for epigenetic dolomitization of the Cambrian host rocks. O isotopes measured in minerals from the first two types (deltaO-18SMOW = 12.8-18.9 parts per thousand) are O-18 depleted with respect to the third type (deltaO-18SMOW = 15.9-22.1 parts per thousand). These data, coupled with fluid inclusion formation temperatures, indicate that the fluids responsible for the first two types of mineralization were O-18 enriched with respect to those of the third type and related hydrothermal phenomena. The deltaS-34CDT in sulfides of the first two types vary between 3.7 and 10.73 per mil, whereas the values of the third type range from 12.0 to 17.9 per mil. Late to post-Hercynian mineralization is thus explained as the result of three distinct, though partly superimposed, hydrothermal systems. System 1 developed closer to the late Hercynian leucogranitic intrusions and led to the formation of the first and subsequently the second type of mineralization. The relatively hot and diluted fluids had a heated meteoric, or even partly magmatic, origin. Metals were leached from an external, radiogenic source, represented either by Hercynian leucogranites or by Paleozoic metasediments. Sulfur had a partly magmatic signature. System 2 was characterized by very saline, colder fluids which promoted dolomitization, silicification, and vein and karst mineralization. These fluids share the typical characteristics of formation waters, even though their origins remain highly speculative. The hydrothermal system was mainly rock dominated, with only a minor participation of the external radiogenic source of metals. Sulfur was derived by recirculation of pre-Hercynian strata-bound ores. System 3 records the invasion of fresh and cold meteoric waters which precipitated only minor ore and calcite gangue. It may represent the further evolution of system 2, possibly spanning a time well after the Permo-Triassic. The timing of all these phenomena is still questionable, due to the poor geologic record of the Permo-Triassic in southwest Sardinia. Nevertheless, the hypothesized scenario bears many similarities with hydrothermal processes documented throughout the Hercynian in Europe and spanning the same time interval. A comparison with the latter mineralization and hydrothermal activities leads to the hypothesis that the first two types of mineralization are linked to late Hercynian magmatic activity, whereas the third type may be related to either strike-slip or tensional tectonics which, throughout Europe mark the transition from the Hercynian orogeny to the Alpine cycle

CHEMICAL-REACTION PATH MODELING OF ORE DEPOSITION IN MISSISSIPPI VALLEY-TYPE PB-ZN DEPOSITS OF THE OZARK REGION UNITED-STATES MIDCONTINENT, 1994, Plumlee G. S. , Leach D. L. , Hofstra A. H. , Landis G. P. , Rowan E. L. , Viets J. G. ,
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

Grottes hydrothermales dans le nord-ouest de la Namibie : splogense et implications dans le dveloppement des karsts en climat aride, 1996, Martini J. E. J. , Marais J. C. E.
The authors investigated ten caves in Western Namibia, which is characterised by a semi- to hyper-arid climate. They seem to have formed in the past under hydrothermal conditions, which are evidenced by circular embayments, ceiling alveoles, avens, deposits of dog-tooth calcite and barite. The latter has been observed in one cave only. Fluid inclusions in calcite and barite indicate very low salinity and temperatures generally below + 70? C. It is proposed that the caves formed by mixing of hydrothermal solutions of deep origin with more surficial ground water in the vicinity of karst springs. Such ground water circulation patterns, close to the water-table, are suggested in several cases by the horizontal extension in caves, forming definite levels of passage networks cutting across the country rock stratigraphy. The alveolar avens developed upwards from these horizontal passages and seem to have formed subaerally by water evaporation from warm pools at the bottom, with condensation and corrosion above, against cooler rock. The suggested genetic processes are in agreement with models proposed by other authors. It is suggested that in arid climates, conditions are more favourable for development of this type of deep karst water circulation than under wetter conditions. It could possibly even be the predominant process of speleogenesis in very arid conditions. By extension, this concept - mixing of water of deep origin, not necessarily significantly hydrothermal with surficial ground water - could explain the peculiar nature of most of the Namibian caves. The latter are typically characterised by the development of very large chambers and phreatic networks, but with restricted extension and not forming well integrated systems.

Brittle tectonics and major dextral strike-slip zone in the Buda karst (Budapest, Hungary), 1999, Benkovics L, Obert D, Bergerat F, Mansy Jl, Dubois M,
Three large (kilometric-scale) caves were studied in the Buda hills and the main directions of cave corridors, fault planes and mineralized veins were measured. Different stages of mineralizations are recognised: calcite scaleno-hedrons, baryte, silica, gypsum. New investigations of fluid inclusions in the baryte suggest a crystallization temperature of 50 degrees C and a freshwater fluid source. Microtectonic analysis allows the reconstruction of the successive tectonic events: (1) a NE-SW extensional phase at the Late Eocene-Early Oligocene limit (phase I), (2) a strike-slip phase with NW-SE compression and NE-SW extension during the Late Oligocene-Early Miocene (phase II), (3) a NW-SE transtensional phase (phase III) and finally (4) a NE-SW extensional phase of Quaternary age (phase IV). The major phase is the strike-slip one, characterized by an important dextral strike-slip zone: the Ferenc-hegy zone. (C) Elsevier, Paris

Vein and Karst Barite Deposits in the Western Jebilet of Morocco: Fluid Inclusion and Isotope (S, O, Sr) Evidence for Regional Fluid Mixing Related to Central Atlantic Rifting, 2000, Valenza Katia, Moritz Robert, Mouttaqi Abdellah, Fontignie Denis, Sharp Zachary,
Numerous vein and karst barite deposits are hosted by Hercynian basement and Triassic rocks of the western Jebilet in Morocco. Sulfur, oxygen, and strontium isotope analyses of barite, combined with fluid inclusion microthermometry on barite, quartz, and calcite were used to reveal the nature and source of the ore-forming fluids and constrain the age of mineralization. The{delta} 34S values of barite between 8.9 and 14.7 per mil are intermediate between the sulfur isotope signatures of Triassic evaporites and Triassic-Jurassic seawater and lighter [IMG]f1.gif' BORDER='0'>, probably derived from the oxidation of dissolved H2S and leaching of sulfides in the Hercynian basement. The 87Sr/86Sr ratios of barite between 0.7093 and 0.7130 range between the radiogenic strontium isotope compositions of micaceous shale and sandstone and the nonradiogenic isotopic signature of Triassic to Jurassic seawater and Cambrian limestone. The{delta} 18O values of barite between 11 and 15 per mil (SMOW) support mixing between two or more fluids, including Late Triassic to Jurassic seawater or a water dissolving Triassic evaporites along its flow path, hot basinal, or metamorphic fluids with{delta} 18O values higher than 0 per mil and/or meteoric fluids with{delta} 18O values lower than 0 per mil. The general trend of decreasing homogenization temperatures and initial ice melting temperatures with increasing salinities of H2O-NaCl {} CaCl2 fluid inclusions trapped in barite, quartz, and calcite indicates that a deep and hot basinal fluid with salinities lower than 6 wt percent NaCl equiv might have mixed with a cooler surficial solution with a mean salinity of 20 wt percent NaCl equiv. Calcium was leached from the Cambrian limestone and the clastic and mafic volcanic rocks of the Hercynian basement. Alkali feldspars and micas contained in the Cambrain sandstones provided most of the Ba to the hydrothermal system. Vein and karst deposits are modeled as a two-component mixing process in which the temperature and the S and Sr isotope composition of the end members changed during the 220 to 155 Ma interval. The hot basinal fluid remained volumetrically dominant during the entire mineralization process. Differences in mean S, O, and Sr isotope compositions among the barite families are interpreted as reflecting differences in mineralization age. Most barite deposits formed before the Kimmeridgian, except for north-south-oriented vein barite, karst barite, and barite cement in the conglomeratic Upper Jurassic, which were deposited later, possibly around 155 Ma. Similar genetic processes have been described for late Paleozoic to Mesozoic F-Ba vein deposits in western Europe. The vein and karst barite in the western Jebilet of Morocco reveals a wide-scale regional mineralization event related to Central Atlantic rifting

Sedimentology and geochemistry of fluvio-lacustrine tufa deposits controlled by evaporite solution subsidence in the central Ebro Depression, NE Spain, 2000, Arenas C, Gutierrez F, Osacar C, Sancho C,
The Urrea de Jalon tufa deposits constitute the 20- to 50-m-thick caprock (0.3 km(2)) of an isolated mesa. They disconformably overlie horizontal strata of the Tertiary Ebro Basin (NE Spain), which contains a thick succession of lacustrine gypsum and marls, followed by limestones, marls and, locally, fluvial sandstones and mudstones. The tufa deposits show a complex, large-scale framework of basin-like structures with centripetal dips that decrease progressively from the base to the top of the tufa succession, and beds that thicken towards the centre of the structure (cumulative wedge-out systems). These geometries reveal that the tufa deposits were affected by differential synsedimentary subsidence. Distinct onlapping depressions reflect time migration of the subsiding areas. The studied carbonates are composed mostly of low-Mg calcite, with minor quartz. Some samples have anomalously high contents of Fe, Mn and Ba that may exceed 1% (goethite, haematite and barite are present). Carbonate facies are: (a) macrophyte encrustation deposits; (b) bryophyte build-ups; (c) oncolite and coated grain rudstones; (d) non-concentric stromatolite-like structures; (e) massive or bioturbated biomicrites; and (f) green and grey marls. Facies a and c show a great variety of microbial-related forms. These facies can be arranged in dm- to 2-m-thick vertical associations representing: (i) fluvial-paludal sequences with bryophyte growths; (ii) pond-influenced fluvial sequences; and (iii) lacustrine-palustrine sequences. The Urrea de Jalon tufa deposits formed in a fluvio-lacustrine environment that received little alluvial sediment supply. Isotope compositions (delta(13)C and delta(18)O) reveal meteoric signatures and accord with such a hydrologically open system of fresh waters. The Fe, Mn and Ba contents suggest an additional supply of mineralized waters that could be related to springs. These would have been discharge points in the Ebro Depression of a regional aquifer of the Iberian Ranges. Rising groundwater caused the solution of the underlying evaporites and the synsedimentary subsidence of the tufa deposits

Origin and Significance of Postore Dissolution Collapse Breccias Cemented with Calcite and Barite at the Meikle Gold Deposit, Northern Carlin Trend, Nevada, 2003, Emsbo P, Hofstra Ah,
The final event in a complicated hydrothermal history at the Meikle gold deposit was gold deficient but caused extensive postore dissolution of carbonate, collapse brecciation, and precipitation of calcite and barite crystals in the resulting cavities. Although previously interpreted to be part of the Carlin-type hydrothermal system, crosscutting relationships and U-Th-Pb geochronology constrain this hydrothermal event to late Pliocene time (ca. 2 Ma), nearly 36 Ma after ore formation. Mineralogic, fluid inclusion, and stable isotope data indicate that postore hydrothermal fluids were reduced, H2S-rich, unevolved meteoric waters ({delta}18O = -17{per thousand}) of low temperature (ca. 65{degrees}C). The{delta} 18O values of barite and calcite indicate that these minerals were in isotopic equilibrium, requiring that barite SO4 was derived from the oxidation of reduced sulfur; however, preexisting sulfides in breccia cavities were not oxidized. The{delta} 34S (15{per thousand}) values of barite are higher than those of local bulk sulfide and supergene alunite indicating that SO4 was not derived from supergene oxidation of local sulfide minerals. The 15 per mil {delta}34S value suggests that the H2S in the fluids may have been leached from sulfur-rich organic matter in the local carbonaceous sedimentary rocks. A reduced H2S-rich fluid is also supported by the bright cathodoluminescence of calcite which indicates that it is Mn rich and Fe poor. Calcite has a narrow range of {delta}13C values (0.3-1.8{per thousand}) that are indistinguishable from those of the host Bootstrap limestone, indicating that CO2 in the fluid was from dissolution of the local limestone. These data suggest that dissolution and brecciation of the Bootstrap limestone occurred where H2S-rich fluids encountered more oxidizing fluids and formed sulfuric acid (H2SO4). Intense fracturing in the mine area by previous structural and hydrothermal events probably provided conduits for the descent of oxidized surface water which mixed with the underlying H2S-rich waters to form the dissolving acid. The surface-derived fluid apparently contained sufficient oxygen to produce H2SO4 from H2S but not enough to alter pyrite to Fe oxide. Although H2S is an important gold-transporting ligand, the temperature was too low to transport a significant amount of gold. The presence of analogous calcite- and barite-lined cavities in other Carlin-type deposits suggests that the generation (and oxidation) of H2S-rich meteoric waters was a common phenomenon in north-central Nevada. Previous sulfur isotope studies have also shown that the Paleozoic sedimentary rocks were the principal source of H2S in Devonian sedimentary exhalative-type, Jurassic intrusion-related, Eocene Carlin-type, and Miocene low-sulfidation gold deposits in the region. The similar sulfur source in all of these systems suggests that basin brines, magmatic fluids, and meteoric waters all evolved to be H2S-rich ore fluids by circulation through Paleozoic sedimentary rocks. Thus, although not directly related to gold mineralization, the recent hydrologic history of the deposit provides important clues to earlier ore-forming processes that were responsible for gold mineralization

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

'Sour gas' hydrothermal jarosite: ancient to modem acid-sulfate mineralization in the southern Rio Grande Rift, 2005, Lueth V. W. , Rye R. O. , Peters L. ,
As many as 29 mining districts along the Rio Grande Rift in southern New Mexico contain Rio Grande Rift-type (RGR) deposits consisting of fluorite-barite sulfide-jarosite, and additional RGR deposits occur to the south in the Basin and Range province near Chihuahua, Mexico. Jarosite occurs in many of these deposits as a late-stage hydrothermal mineral coprecipitated with fluorite, or in veinlets that crosscut barite. In these deposits, many of which are limestone-hosted, jarosite is followed by natrojarosite and is nested within silicified or argillized wallrock and a sequence of fluorite-barite sulfide and late hematite-gypsum. These deposits range in age from similar to 10 to 0.4 Ma on the basis of Ar-40/Ar-39 dating of jarosite. There is a crude north-south distribution of ages, with older deposits concentrated toward the south. Recent deposits also occur in the south, but are confined to the central axis of the rift and are associated with modem geothermal systems. The duration of hydrothermal jarosite mineralization in one of the deposits was approximately 1.0 my. Most Delta(18)O(SO4)-OH values indicate that jarosite precipitated between 80 and 240 degrees C, which is consistent with the range of filling temperatures of fluid inclusions in late fluorite throughout the rift, and in jarosite (180 degrees C) from Pena Blanca, Chihuahua, Mexico. These temperatures, along with mineral occurrence, require that the jarosite have had a hydrothermal origin in a shallow steam-heated environment wherein the low pH necessary for the precipitation of jarosite was achieved by the oxidation of H2S derived from deeper hydrothermal fluids. The jarosite also has high trace-element contents (notably As and F), and the jarosite parental fluids have calculated isotopic signatures similar to those of modem geothermal waters along the southern rift; isotopic values range from those typical of meteoric water to those of deep brine that has been shown to form from the dissolution of Permian evaporite by deeply circulating meteoric water. Jarosite delta(34)S values range from -24 parts per thousand to 5 parts per thousand, overlapping the values for barite and gypsum at the high end of the range and for sulfides at the low end. Most delta(34)S values for barite are 10.6 parts per thousand to 13.1 parts per thousand and many delta(34)S values for gypsum range from 13.1 parts per thousand to 13.9 parts per thousand indicating that a component of aqueous sulfate was derived from Permian evaporites (delta(34)S = 12 2 parts per thousand). The requisite H2SO4 for jarosite formation was derived from oxidation of H2S which was likely largely sour gas derived from the thermochemical reduction of Permian sulfate. The low delta(34)S values for the precursor H2S probably resulted from exchange deeper in the basin with the more abundant Permian SO42-- at similar to 150 to 200 degrees C. Jarosite formed at shallow levels after the PH buffering capacity of the host rock (typically limestone) was neutralized by precipitation of earlier minerals. Some limestone-hosted deposits contain caves that may have been caused by the low pH of the deep basin fluids due to the addition of deep-seated HF and other magmatic gases during periods of renewed rifting. Caves in other deposits may be due to sulfuric acid speleogenesis as a result of H2S incursion into oxygenated groundwaters. The isotopic data in these 'sour gas' jarosite occurrences encode a recod of episodic tectonic or hydrologic processes that have operated in the rift over the last 10 my. (c) 2004 Elsevier B.V. All rights reserved

Mineralogical and Stable Isotope Studies of Kaolin Deposits: Shallow Epithermal Systems of Western Sardinia, Italy, 2005, Simeone R. , Dilles J. H. , Padalino G. , Palomba M. ,
Large kaolin deposits hosted by Miocene silicic pyroclastic rocks in northwestern Sardinia represent hydrothermal alteration formed within 200 m of the Miocene paleosurface. Boiling hydrothermal fluids ascended steeply dipping faults that are enveloped by altered rock. The broadly stratiform kaolin deposits constitute advanced argillic alteration that was produced in a steam-heated zone near the paleosurface overlying the deeper hydrothermal systems. The deeper zones represent two distinct types of epithermal systems: weakly acidic (inferred low-sulfidation) systems at Tresnuraghes and acidic (high-sulfidation) systems at Romana. Tresnuraghes is characterized at depth by chalcedony {} quartz {} barite veins within a 50-m-wide zone of K-feldspar-quartz-illite alteration and overlying local occurrences of chalcedony sinter, which define the paleosurface. Kaolin deposits near the paleosurface are characterized by zonation outward and downward from an inner shallow zone of kaolinite 1T-opal {} dickite {} alunite (<20-{micro}m-diam grains) to an outer deeper kaolinite 1M-montmorillonite-cristobalite. This zonation indicates formation by descending acidic fluids. The system evolved from ascending weakly acidic or neutral fluids that boiled to produce H2S-rich vapor, which condensed and oxidized within the near-surface vadose zone to form steam-heated acid-sulfate waters and kaolin alteration. At Romana, veins at depth contain chalcedony or quartz and minor pyrite and are enclosed in up to 20-m-wide zones of kaolinite 1T-quartz alteration. Near hydrothermal vents along the paleosurface, chalcedonic silica is enclosed within a zone of kaolinite 1T-alunite (<50-{micro}m-diam grains)-quartz-opal {} dickite {} cristobalite. Kaolin quarries near the paleosurface display outward and downward zoning to kaolinite 1T-opal {} cristobalite and then to montmorillonite-kaolinite 1T {} opal, consistent with formation by descending low pH fluid. The siliceous and advanced argillic alteration along steep conduits formed from acidic ascending magmatic-hydrothermal fluids, whereas the near-surface kaolin formed from steam-heated meteoric waters. Alteration mineral assemblages and stable isotope data provide evidence of the temperature and source of hydrothermal fluids. Barite from Tresnuraghes (average{delta} 18O = 17.1{per thousand},{delta} 34S = 18.8{per thousand}), one alunite sample from Romana ({delta}18O = 12.0{per thousand},{delta} D = -3{per thousand},{delta} 34S = 16.7{per thousand}), and quartz from both localities ({delta}18O = 15.9-22.0{per thousand}) formed in hydrothermal feeders. Source fluids were likely mixtures of meteoric water and minor magmatic fluid, similar to other epithermal systems. Kaolinite-dickite minerals from the kaolin deposits ({delta}18O = 16.6-21.4{per thousand},{delta} D = -43 to -53{per thousand}) formed from steam-heated meteoric water having{delta} D = - 20 per mil, consistent with the presence of anomalous Hg and fine-grained Na- and Fe-poor alunite. The laterally extensive kaolin deposits in Sardinia, and possibly similar deposits elsewhere in the world, appear to represent the uppermost parts of large hydrothermal systems that may be prospects for gold at depth

Fluid inclusion study of a sedimentary basin: an example of Culberson sulfur and barite deposit, Texas, 2006, Lu H. Z. ,
The Culberson sulfur-barite deposit is located in Culberson county, West Texas. Geologically, it is occurred ill Delaware sedimentary, petroleum and natural gas basin. There are several sulfur-barite deposits occurring in the basin, Culberson is the largest one. Culberson deposit is hosted by Upper Permian Castile and Salado formation. The Castile and Salodo formation consist of limestone with thin layers of evaporate and organic materials. Natural sulfur and barite is formed post diagenesis, filled into the palco karst and replaced the internal layers of anhydrite. Two generation fluid inclusions are found: I. Fluid inclusion formed during the diagenesis, and II. Fluid inclusion trapped during the authigenic calcite, barite overgrowth. According to the phases and composition at room temperature, the fluid inclusions could be divided into: one phase liquid inclusion; two phases vapor and liquid inclusion, and oil inclusion. In a same growth zone of calcite, several types of fluid inclusions, such as one phase liquid, different vapor/liquid ratio inclusions and oil inclusions occurred. These inclusions are hardly to he used to gel the temperature of homogenization, since they are formed in heterogeneous trapping or an immiscibility environment. The eutectic temperatures of fluid inclusions range from -18 to -24 degrees C, indicating life fluid belongs to a NaCl-H2O system, with the salinity ranges from 2% to 10%, and co-existing with the oil inclusions, these show that the ore forming fluid is an oil filed brine and with temperature less than 100 degrees C

Reactive transport modeling and hydrothermal karst genesis: The example of the Rocabruna barite deposit (Eastern Pyrenees), 2006, Corbella M, Ayora C, Cardellach E, Soler A,
In western Europe and North Africa, many sulfide and barite deposits appear to be related to the pre-Triassic paleosurface. Some of these mineralizations have traditionally been interpreted as the result of mineral fillings of previously formed karstic cavities. However, reactive transport modeling suggests that those minerals may have originated at depth and simultaneous with the cavity in the carbonate rocks. Numerical simulations using the Rocabruna deposit as an example recreate the genesis of such cavities and their filling by new minerals in a hydrothermal environment. Two warm (T = 150 [deg]C) fluids with different compositions but both saturated with dolomite were allowed to mix at a fracture intersection; the resulting solution strongly corroded the dolomite host rock and was able to create large voids in a hundred thousand year time scale. Our results show that equidimensional cavities originate from mixtures with equal fluxes of the contributing fluids, but elongated dissolution zones appear when the flux ratios were different from unity and the slowest flow direction coincided with the longest dimension of the void. Moreover, when the fluid mixture was dominated by a diluted and slightly alkaline groundwater instead of a 50-50 mixture with an acidic brine, dolomite dissolution or corrosion was more effective. Sulfide minerals precipitate around cavity walls replacing the host dolostone as the dolomite dissolution reaction couples with that of sulfide precipitation. This coupling produces some porosity, which is negligible compared to that caused by the mixing itself. Barite may also precipitate inside the forming cavity, but as the sulfate mineral precipitation reaction is not coupled with that of dolomite dissolution, barite grows in open space

Results 1 to 15 of 25
You probably didn't submit anything to search for