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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. ...

Did you know?

That glaciokarst is 1. a karst landscape that was glaciated during the cold periods of the pleistocene and displays major landforms of relict glacial origin. bare rock scars, locally with glacial striations, and limestone pavements are characteristic, due to the lack of rapid soil formation on the limestones since glacial stripping. dolines within a glaciokarst are mostly small and immature, as are caves, except where pre-glacial passages are intercepted. glaciokarst is almost synonymous with alpine karst, and some of the finest is developed on the high plateaus of the calcareous alps, south of salzburg, austria [9]. 2. a glaciated limestone region possessing both glacial and karst characteristics [10]. (french.) karst glaciaire; (german.) gebiet mit karst und glazial-formen; (greek.) pagheto-karst; (spanish.) glaciokarst; (turkish.) buzul karsti; (yugoslavian.) glaciokrs, glaciokras, glaciokarst. see also alpine karst; nival karst.?

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Featured articles from Cave & Karst Science Journals
Chemistry and Karst, White, William B.
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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;
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Your search for fluid inclusions (Keyword) returned 43 results for the whole karstbase:
Showing 1 to 15 of 43
Identification of the origin of oreforming solutions by the use of stable isotopes, 1977, Sheppard S. M. F. ,
SynopsisThe four major different types of water -- magmatic, metamorphic, sea water and/or connate, and meteoric water -- have characteristic hydrogen (D/H) and oxygen (18O/16O) isotope ratios. Applied to the analysis of isotopic data on hydrothermal minerals, fluid inclusions and waters from active geothermal systems, these ratios indicate that waters of several origins are involved with ore deposition in the volcanic and epizonal intrusive environment. Water of a single origin dominates main-stage mineralization in some deposits: magmatic -- Casapalca, Peru (Ag-Pb-Zn-Cu); meteoric -- Butte, Montana (Cu-Zn-Mn), epithermal deposits, e.g. Goldfield, Tonopah, Nevada (Ag-Au), Pachuca, Mexico (Ag-Au), San Juan Mountains District, Colorado (Ag-Au-Pb-Zn); sea water -- Troodos, Cyprus (Fe-Cu), Kuroko, Japan (Fe-Cu-Pb-Zn). Solutions of more than one origin are important in certain deposits (magmatic and meteoric -- porphyry copper and molybdenum deposits) and are present in many. In the porphyry Cu-Mo deposits the initial major ore transportation and alteration processes (K-feldspar-biotite alteration) are magmatic-hydrothermal events that occur at 750-500{degrees}C. These fluids are typically highly saline Na-K-Ca-Cl-rich brines (more than 15 wt % equivalent NaCl). The convecting meteoric-hydrothermal system that develops in the surrounding country rocks with relatively low integrated water/rock ratios (less than 0.5 atom % oxygen) subsequently collapses in on a waning magmatic-hydrothermal system at about 350-200{degrees}C. These fluids generally have moderate to low salinities (less than 15 wt % equivalent NaCl). Differences among these deposits are probably in part related to variations in the relative importance of the meteoric-hydrothermal versus the magmatic-hydrothermal events. The sulphur comes from the intrusion and possibly also from the country rocks. Deposits in which meteoric or sea water is the dominant constituent of the hydrothermal fluids come from epizonal intrusive and sub-oceanic environments where the volcanic country rocks are fractured or well jointed and highly permeable. Integrated water/rock ratios are typically high, with minimum values of 0.5 or higher (atom % oxygen) -- the magmatic water contribution is often drowned out'. Salinities are low to very low (less than 10 wt % equivalent NaCl), and temperatures are usually in the range 350-150{degrees}C. The intrusion supplies the energy to drive the large-scale convective circulation system. The sulphur comes from the intrusion, the country rocks and/or the sea water. Argillic alteration, which occurs to depths of several hundred metres, generated during supergene weathering in many of these deposits is isotopically distinguishable from hydrothermal clays

Secondary Origin of the Radial Fabric in Stalactitic Carbonate., 1983, Broughton Paul L.
The growth surfaces of most stalactites are interpreted as numerous syntaxial overgrowth crystallites. These coalesce immediately behind the growth surface, often trapping portions of the water film as fluid-filled cavities. The fluid inclusions represent former inter-crystallite spaces and characterize the widely misinterpreted "growth ring". Complete crystallite coalescence generates inclusions-free calcite, whereas inhibition of lateral coalescence of the overgrowth crystallites generates layers of acicular calcite. It is generally only during periods of cave flooding that the crystallites merge and overgrow each other and precipitation eventually occurs upon large, planar crystal faces. Stalactitic carbonate growth is secondary, from a multi-crystalline precursor that is, in a sense, a largo skeletal crystal. The precursor crystallites are in lattice continuity with the substrate and with adjacent crystallites. Crystal boundaries arise from lateral lattice mismatch on the curved growth surface. It is not competitive growth as the secondary columnar crystals do not interfere with each other.

Petrographic and geochemical evidence for origin of paleospeleothems, New Mexico; implications for the application of fluid inclusions to studies of diagenesis, 1990, Goldstein Robert H. ,

DIAGENESIS AND MINERALIZATION PROCESSES IN DEVONIAN CARBONATE ROCKS OF THE SIDING-GUDAN LEAD-ZINC MINERAL SUBDISTRICT, GUANGXI, SOUTHWEST CHINA, 1991, Schneider W. , Geng A. Q. , Liu X. Z. ,
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

Palaeoclimate determination from cave calcite deposits, 1992, Gascoyne M,
Calcite deposits formed in limestone caves have been found to be an excellent repository of palaeoclimatic data for terrestrial environments. The very presence of a relict deposit indicates non-glacial conditions at the time of formation, and both 14C and uranium-series methods can be used to date the deposit and, hence, the age of these climatic conditions. Variations in 13C and 18O content of the calcite, in 2H and 18O content of fluid inclusions, in trace element concentrations and, more recently, in pollen assemblages trapped in the calcite, are all potentially available as synchronous palaeoclimatic indicators. Previous work has tended to concentrate mainly on abundance of deposits as a palaeoclimatic indicator for the last 300,000 years. This literature is briefly reviewed here, together with the theory and methods of analysis of the U-series and stable isotopic techniques. The combined use of U-series ages and 13C and 18O variations in cave calcites illustrates the potential for palaeoclimate determination. Previously unpublished results of stable isotopic variations in dated calcites from caves in northern England indicate the level of detail of stable isotopic variations and time resolution that can be obtained, and the complexity of interpretation that may arise. Tentative palaeoclimatic signals for the periods 90-125 ka and 170-300 ka are presented. More comprehensive studies are needed in future work, especially in view of the difficulty in obtaining suitable deposits and the ethics of cave deposits conservation

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

The role of evaporites in the genesis of base metal sulphide mineralisation in the Northern Platform of the Pan-African Damara Belt, Namibia: geochemical and fluid inclusion evidence from carbonate wa, 2000, Chetty D, Frimmel He,
The Otavi Mountain Land is a base metal sulphide ore province in northern Namibia where deposits are hosted by platform carbonates of the Otavi Group in a foreland fold-and-thrust belt on the northern edge of the Pan-African Damara Belt. Deposits have been classified as the Berg Aukas- or Tsumeb-types, based on differences in ore association? stratigraphic position and geochemistry of ores and gangue carbonates. Mineralisation at these deposits is accompanied by carbonate alteration in the form of dolomite and calcite veins, carbonate recrystallisation, calcitisation and carbonate silicification. Based on cathodoluminescence imaging, trace and rare earth element (REE), O and C isotope, and fluid inclusion data, a series of carbonate generations, constituting wall rock alteration around the Tsumeb and Kombat (Tsumeb-type) and Berg Aukas (Berg Aukas-type) deposits, was established. Similar data obtained on the recently discovered Khusib Springs deposit indicate a strong affinity to Tsumeb-type deposits. Tsumeb-type deposits are distinguished from Berg Aukas-type deposits by having trace element and REE concentrations that are significantly higher in the alteration products compared to the carbonate host rocks. Only around Tsumeb-type deposits a relative enrichment in light REE is noted for the hydrothermal carbonate generations that are cogenetic with the main stage of mineralisation. Microthermometric results from fluid inclusions in carbonate alteration phases and associated quartz indicate relatively high salinity (17-33 wt% NaCl equivalent) for the main mineralising and subsequent sulphide remobilisation stages at the deposits investigated. Estimated mineralisation temperatures are significantly higher for Tsumeb-type deposits (370-405 degrees C) with early sulphide remobilisation in Tsumeb at 275 degrees C, whereas they are lower at Berg Aukas (up to 255 degrees C). Fluid inclusion leachate analysis suggests that most of the observed salinity can be ascribed to dissolved, predominantly Ca- and Mg-carbonates and chlorides with subordinate NaCl. Na-Cl-Br leachate systematics indicate a derivation of the fluid salinity from the interaction with evaporitic rocks en route. Tsumeb-type mineralisation is interpreted to be derived from fluids expelled during Pan-African orogeny in the more intensely deformed internal zones of the Damara Belt further south. When the high salinity fluids reached the carbonate platform after having scavenged high concentrations of base metals, base metal sulphide precipitation occurred in zones of high porosity, provided by karst features in the carbonate sequence. Results obtained for the Berg Aukas-type deposits emphasise their derivation from basinal brines, similar to Mississippi Valley-type deposits, and confirm that mineralisation of the Berg Aukas- and Tsumeb-types are both spatially and temporally distinct

Geochemical study of calcite veins in the Silurian and Devonian of the Barrandian Basin (Czech Republic): evidence for widespread post-Variscan fluid flow in the central part of the Bohemian Massif, 2000, Suchy V. , Heijlen W. , Sykorova I. , Muchez Ph. , Dobes P. , Hladikova J. , Jackova I. , Safanda J. , Zeman A.

Carbonate fracture cements in limestones have been investigated by fluid inclusion and stable isotope analysis to provide insight into fluid evolution and deformation conditions of the Barrandian Basin (Silurian–Devonian) of the Czech Republic. The fractures strike generally north–south and appear to postdate major Variscan deformation. The most common fracture cement is calcite that is locally accompanied by quartz, natural bitumen, dolomite, Mn-oxides and fluorite. Three successive generations of fracture-filling calcite cements are distinguished based on their petrographical and geochemical characteristics. The oldest calcite cements (Stage 1) are moderate to dull brown cathodoluminescent, Fe-rich and exhibit intense cleavage, subgrain development and other features characteristic of tectonic deformation. Less tectonically deformed, variable luminescent Fe-poor calcite corresponds to a paragenetically younger Stage 2 cement. First melting temperatures, Te, of two-phase aqueous inclusions in Stages 1 and 2 calcites are often around 2208C, suggesting that precipitation of the cements occurred from H2O–NaCl fluids. The melting temperature, Tm, has values between 0 and 25.88C, corresponding to a low salinity between 0 and 8.9 eq. wt% NaCl. Homogenization temperatures, Th, from calcite cements are interpreted to indicate precipitation at about 708C or less. No distinction could be made between the calcite of Stages 1 and 2 based on their fluid inclusion characteristics. In some Stage 2 cements, inclusions of highly saline (up to 23 eq. wt% NaCl) brines appear to coexist with low-salinity inclusions. The low salinity fluid possibly contains Na-, K-, Mg- and Ca-chlorides. The high salinity fluid has a H2O–NaCl–CaCl2 composition. Blue-to-yellow-green fluorescing hydrocarbon inclusions composed of medium to higher API gravity oils are also identified in some Stages 1 and 2 calcite cements. Stage 1 and 2 calcites have d 18O values between 213.2‰ and 27.2‰ PDB. The lower range of the calculated d 18O values of the ambient fluids (23.5‰ to 1 2.7‰ SMOW) indicate precipitation of these cements from deeply circulating meteoric waters. The presence of petroleum hydrocarbon inclusions in some samples is interpreted to reflect partial mixing with deeper basinal fluids. The paragenetically youngest Stage 3 calcite cement has only been encountered in a fewveins.These calcites are characterised by an intensely zoned luminescence pattern, with bright yellow and non-luminescent zones. Inclusions of Mn-oxides and siliceous sinters are commonly associated with Stage 3 calcite, which is interpreted to have precipitated from shallower meteoric waters. Regional structural analysis revealed that the calcite veins of the Barrandian basin belong to a large-scale system of north–south-trending lineaments that run through the territory of the Czech Republic. The veins probably reflect episodes of fluid migration that occurred along these lineaments during late stages of the Variscan orogeny


Sedimentologic, diagenetic and tectonic evolution of the Saint-Flavien gas reservoir at the structural front of the Quebec Appalachians, 2003, Bertrand R, Chagnon A, Malo M, Duchaine Y, Lavoie D, Savard Mm,
The Beekmantown Group (Lower Ordovician) of the Saint-Flavien reservoir has produced 162x106 m3 (5.7 bcf) of natural gas between 1980 and 1994. The conversion of the field into gas storage was initiated in 1992 and the pool became operational in 1998. Integration of structural and sedimentologic features, carbonate and organic matter petrography and geochemistry for 13 drill holes is used to define a tectonic-sedimentologic-diagenetic model for porosity evolution in these reservoir dolostones. The Beekmantown Group consists of numerous fifth-order shallowing-upward cycles 1.0 to 7.0 m thick (average of 2.4 m). Each cycle consists of a basal shale deposited during the initial flooding of the platform which was subsequently covered by a shoaling succession of subtidal and intertidal limestones to intertidal dolostones. Early dolomitization has produced intercrystalline porosity and preserved some moldic pores in the intertidal facies. Near surface, post-dolomite karstification has created vugs that were subsequently filled by early marine calcite fibrous cement based on the {delta}18O and {delta}13C ratios of calcite. Early burial elements consist of horizontal stylolites, pyrite and sphalerite. Late migrated bitumen was thermally altered or vaporized as native coke under deep burial conditions exceeding 240{degrees}C, partly due to overthrusting of Appalachian nappes. Under these conditions, breccias and fractures were generated and subsequently filled with K-feldspar, quartz, illite, and xenomorphic and poikilotopic calcite. The {delta}18O of the poikilotopic calcite and homogenization temperature of coeval fluid inclusions indicate formation under high temperatures (Th about 260{degrees}C). Horizontal shear zones and marcasite-rich vertical stylolites were produced during folding and thrusting. Dissolution has preferentially affected late fracture-filling calcite and generated most of the actual porosity during or soon after the Taconian Orogeny. The relationship between the occurrence of smectite and this type of porosity indicates the low temperature condition of this dissolution (T <100{degrees}C). Porosity in the Saint-Flavien reservoir has been mostly produced by fracture-controlled, late to post-Taconian dissolution of early to late calcite in the intertidal dolomitic slightly porous facies at the top of rhythmic cycles that compose the Beekmantown Group

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

Fluid inclusion and stable isotopic evidence for early hydrothermal karstification in vadose caves of the Nizke Tatry Mountains (Western Carpathians), 2004, Orvosova M. , Hurai V. , Simon K. , Wiegerova V. ,
Hydrothermal paleokarst cavities with calcite crystals up to 20 cm in diameter were found in two caves of the Nizke Tarry Mountains developed in Triassic limestone and dolomite of the Guttenstein type. In both caves, older zones of tectonic and hydrothermal activity have been overprinted by vadose speleogenesis. According to fluid inclusion microthermometry data, prismatic-scalenoliedral calcite from the Silvo ova Diera Cave has precipitated at temperatures between similar to60 and 101degreesC from low salinity aqueous solutions (less than or equal to0.7 wt. % NaCl eq.). Carbon and oxygen isotope profiling revealed significant delta(13)C decrease accompanied by slight delta(18)O increase during growth of calcite crystals. The negatively correlated carbon and oxygen isotope data cannot be interpreted in terms of any geologically reasonable models based on equilibrium isotopic fractionation. Fluid inclusion water exhibits minor decrease of deltaD values from crystal core (-31 %o SMOW) to rim (-41 %(0) SMOW). Scalenohedral calcite from the NovA Stanisovska Cave has precipitated at slightly higher temperatures 63-107degreesC from aqueous solutions with salinity : less than or equal to2.7 % NaCl eq. The positively correlated trend of delta(13)C and delta(18)O values is similar to common hydrothermal carbonates. The fluid inclusion water deltaD values differ significantly between the crystal core (-50 %(0) SMOW) and rim (- 11 %o SMOW). The calcite crystals are interpreted as representing a product of an extinct hydrothermal system, which was gradually replaced by shallow circulation of meteoric water. Fossil hydrothermal fluids discharged along Alpine uplift-related NNW-SSE-trending faults in Paleogene-pre-Pliocene times. Increased deuterium concentration in the inclusion water compared to recent meteoric precipitation indicates a warmer climate during the calcite crystallization

Concepts and models of dolomitization: a critical reappraisal, 2004, Machel Hans G. ,
Despite intensive research over more than 200 years, the origin of dolomite, the mineral and the rock, remains subject to considerable controversy. This is partly because some of the chemical and/or hydrological conditions of dolomite formation are poorly understood, and because petrographic and geochemical data commonly permit more than one genetic interpretation. This paper is a summary and critical appraisal of the state of the art in dolomite research, highlighting its major advances and controversies, especially over the last 20-25 years. The thermodynamic conditions of dolomite formation have been known quite well since the 1970s, and the latest experimental studies essentially confirm earlier results. The kinetics of dolomite formation are still relatively poorly understood, however. The role of sulphate as an inhibitor to dolomite formation has been overrated. Sulphate appears to be an inhibitor only in relatively low-sulphate aqueous solutions, and probably only indirectly. In sulphate-rich solutions it may actually promote dolomite formation. Mass-balance calculations show that large water/rock ratios are required for extensive dolomitization and the formation of massive dolostones. This constraint necessitates advection, which is why all models for the genesis of massive dolostones are essentially hydrological models. The exceptions are environments where carbonate muds or limestones can be dolomitized via diffusion of magnesium from seawater rather than by advection. Replacement of shallow-water limestones, the most common form of dolomitization, results in a series of distinctive textures that form in a sequential manner with progressive degrees of dolomitization, i.e. matrix-selective replacement, overdolomitization, formation of vugs and moulds, emplacement of up to 20 vol% calcium sulphate in the case of seawater dolomitization, formation of two dolomite populations, and -- in the case of advanced burial -- formation of saddle dolomite. In addition, dolomite dissolution, including karstification, is to be expected in cases of influx of formation waters that are dilute, acidic, or both. Many dolostones, especially at greater depths, have higher porosities than limestones, and this may be the result of several processes, i.e. mole-per-mole replacement, dissolution of unreplaced calcite as part of the dolomitization process, dissolution of dolomite due to acidification of the pore waters, fluid mixing (mischungskorrosion), and thermochemical sulphate reduction. There also are several processes that destroy porosity, most commonly dolomite and calcium sulphate cementation. These processes vary in importance from place to place. For this reason, generalizations about the porosity and permeability development of dolostones are difficult, and these parameters have to be investigated on a case-by-case basis. A wide range of geochemical methods may be used to characterize dolomites and dolostones, and to decipher their origin. The most widely used methods are the analysis and interpretation of stable isotopes (O, C), Sr isotopes, trace elements, and fluid inclusions. Under favourable circumstances some of these parameters can be used to determine the direction of fluid flow during dolomitization. The extent of recrystallization in dolomites and dolostones is much disputed, yet extremely important for geochemical interpretations. Dolomites that originally form very close to the surface and from evaporitic brines tend to recrystallize with time and during burial. Those dolomites that originally form at several hundred to a few thousand metres depth commonly show little or no evidence of recrystallization. Traditionally, dolomitization models in near-surface and shallow diagenetic settings are defined and/or based on water chemistry, but on hydrology in burial diagenetic settings. In this paper, however, the various dolomite models are placed into appropriate diagenetic settings. Penecontemporaneous dolomites form almost syndepositionally as a normal consequence of the geochemical conditions prevailing in the environment of deposition. There are many such settings, and most commonly they form only a few per cent of microcrystalline dolomite(s). Many, if not most, penecontemporaneous dolomites appear to have formed through the mediation of microbes. Virtually all volumetrically large, replacive dolostone bodies are post-depositional and formed during some degree of burial. The viability of the many models for dolomitization in such settings is variable. Massive dolomitization by freshwater-seawater mixing is a myth. Mixing zones tend to form caves without or, at best, with very small amounts of dolomite. The role of coastal mixing zones with respect to dolomitization may be that of a hydrological pump for seawater dolomitization. Reflux dolomitization, most commonly by mesohaline brines that originated from seawater evaporation, is capable of pervasively dolomitizing entire carbonate platforms. However, the extent of dolomitization varies strongly with the extent and duration of evaporation and flooding, and with the subsurface permeability distribution. Complete dolomitization of carbonate platforms appears possible only under favourable circumstances. Similarly, thermal convection in open half-cells (Kohout convection), most commonly by seawater or slightly modified seawater, can form massive dolostones under favourable circumstances, whereas thermal convection in closed cells cannot. Compaction flow cannot form massive dolostones, unless it is funnelled, which may be more common than generally recognized. Neither topography driven flow nor tectonically induced ( squeegee-type') flow is likely to form massive dolostones, except under unusual circumstances. Hydrothermal dolomitization may occur in a variety of subsurface diagenetic settings, but has been significantly overrated. It commonly forms massive dolostones that are localized around faults, but regional or basin-wide dolomitization is not hydrothermal. The regionally extensive dolostones of the Bahamas (Cenozoic), western Canada and Ireland (Palaeozoic), and Israel (Mesozoic) probably formed from seawater that was pumped' through these sequences by thermal convection, reflux, funnelled compaction, or a combination thereof. For such platform settings flushed with seawater, geochemical data and numerical modelling suggest that most dolomites form(ed) at temperatures around 50-80 {degrees}C commensurate with depths of 500 to a maximum of 2000 m. The resulting dolostones can be classified both as seawater dolomites and as burial dolomites. This ambiguity is a consequence of the historical evolution of dolomite research

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