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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. ...

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. ...

Speleology in Kazakhstan

Shakalov on 11 Jul, 2012
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 calcite is 1. the commoner, more stable, mineral form of calcium carbonate, caco3. it is the dominant component of all limestones and, due to its dissolution and reprecipitation by natural waters at normal temperatures, it is also the dominant mineral of chemical cave deposits including stalactites and stalagmites. it is white or colorless when pure but may be stained, most commonly to yellows and browns, by included impurities such as iron oxides. its uninterrupted growth in a pool may allow development of good crystals, shaped as elongate scalenohedral pyramids of trigonal habit. growth in stalactites and stalagmites is either in masses of fine parallel or radiating needles, or in a mosaic of larger rhombic crystals, easily identified by their well developed cleavage surfaces. calcite is also the dominant vein mineral in limestones [9]. 2. a mineral composed of calcium carbonate (caco3) like aragonite but differing in crystal form; the principal constituent of limestone and other speleothems [10].?

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Featured articles from Cave & Karst Science Journals
Chemistry and Karst, White, William B.
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Geochemical and mineralogical fingerprints to distinguish the exploited ferruginous mineralisations of Grotta della Monaca (Calabria, Italy), Dimuccio, L.A.; Rodrigues, N.; Larocca, F.; Pratas, J.; Amado, A.M.; Batista de Carvalho, L.A.
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
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Your search for water-rock interaction (Keyword) returned 25 results for the whole karstbase:
Showing 1 to 15 of 25
RELATION OF MINERALIZATION TO WALL-ROCK ALTERATION AND BRECCIATION, MASCOT JEFFERSON-CITY MISSISSIPPI-VALLEY-TYPE DISTRICT, TENNESSEE, 1994, Haynes F. M. , Keslr S. E. ,
This study was undertaken to assess the relation of Mississippi Valley-type mineralization to wall-rock alteration and brecciation in the Mascot-Jefferson City district, the largest part of the East Tennessee Mississippi Valley-type ore field. The main question of interest was whether the Mississippi Valley-type-forming brines created or greatly enlarged the breccia system that hosts the ore or whether the breccia system was a preexisting paleoaquifer that simply controlled movement of the mineralizing brines. A secondary, and closely related, question was whether brine-wall rock interaction deposited Mississippi Valley-type ore. The breccia system that hosts the East Tennessee ore field began as karst breccias which formed in the upper part of the Late Cambrian-Early Ordovician Knox Group during Middle Ordovician emergence. Brecciation, which was most common at the paleosurface and in a limestone-rich zone about 200 m below the surface, took place when limestone solution caused collapse of primary dolostone layers. Mississippi Valley-type mineralization, consisting of sphalerite and sparry dolomite, fills interstices in the breccias that formed in the limestone-rich part of the Knox Group. Ore is associated with ''recrystalline dolomite'' that replaced limestone and there is an inverse correlation between the original limestone and sphalerite abundance suggesting that the ore-forming fluids reacted strongly with limestone wall rock, possibly dissolving it where alteration was most intense. The assessment of a relation between alteration and Mississippi Valley-type mineralization was based on 3,533 surface drill holes covering the 110-km2 Mascot-Jefferson City district, each of which provided stratigraphic data and quantified estimates of mineralization intensity and alteration intensity. These data show clearly that as much as 50 percent of the limestone in the mineralized breccia section was lost over enormous areas that extend far beyond significant mineralization. The intensity of this effect clearly decreases downdip (toward the east), away from the probable source of meteoric karst-forming waters. These relations, combined with isotopic analyses and reaction path calculations, suggest that breccia formation and limestone dissolution took place during the original karst breccia formation. In contrast, later Mississippi Valley-type mineralization was associated with replacement of limestone by recrystalline dolomite. The main effect of dolomitization on the chemistry of the Mississippi Valley-type brines, an increase in their Ca/Mg ratio, would not cause sulfide precipitation. Thus, it appears unlikely that Mississippi Valley-type-forming brines created much of their ore-hosting breccias or that water-rock interaction was a major cause of Mississippi Valley-type ore deposition

MICROBIOLOGICAL ACTIVITY IN THERMOGLACIAL KARST SPRINGS, SOUTH SPITSBERGEN, 1994, Lauritzen S. E. , Bottrell S. ,
Along the Hornsund fault zone, South Spitsbergen (76-degrees-60'N), thermokarstic springs smell of H2S and display either growth of, or eject fragments of, organic slime. The temperature in individual springs varies between 4 and 15-degrees-C. Their rate of discharge is approximately 1 L s-1 to 18 m3 s-1, corresponding to a minimum temperature of 30-degrees-C within the base of the aquifer. The water, which contains a few ppm SO4(2-), 0.5 ppm S2-, and several thousand ppm NaCl, appears to be a mixture of turbid glacial meltwater and hot brine. Water chemistry and stable isotopes indicate that the salinity is not the result of simple dilution of modern seawater from the brackish zone beneath the coastal karst aquifer, but rather originates from a deep thermal brine component where concentrations and isotopic composition of various species are controlled by water-rock interaction in the source area of the brine. A value of DELTAdeltaS-34 of up to about 30 parts per thousand indicates that sulfide is a bioreduction product of sulfate. Scanning electron microscope (SEM) studies revealed bacteria and fungal hypha in the organic slime, and larger spherical particles (approximately 3.8 mum diameter) that display high concentrations of Fe and S. These findings demonstrate the presence of sulfate-reducing bacteria within the subpermafrost aquifer

HYDROGEOCHEMISTRY OF GRAND-CAYMAN, BRITISH-WEST-INDIES - IMPLICATIONS FOR CARBONATE DIAGENETIC STUDIES, 1995, Ng K. C. , Jones B. ,
Groundwater in the dolostone aquifers of the Bluff Group (Oligocene-Miocene) on Grand Cayman is divided into fresh, lightly and highly brackish, and saline (Type I and II) zones according to chemical characteristics that were determined during a 3 year (1985-1988) monitoring program. Brackish and Type I saline waters display the greatest variation in chemical properties whereas the Type II saline water has the most stable chemical characteristics. Most groundwaters from these dolostone aquifers are thermodynamically capable of precipitating calcite and/or dolomite. The saturation indices for these minerals, however, vary through time and space even in the context of small water lens. Simple mixing of fresh and sea water cannot explain the chemistry of the water found in the joint and karst controlled dolostone aquifers of Grand Cayman. Deviation from a simple mixing model is due to variations caused by tidal fluctuation, the rate of rain water recharge, influx of Ca-rich groundwater from the surrounding limestone aquifers, influx of CO2-rich surface water from sinkholes and swamps, and water-rock interactions (dissolution and precipitation of calcite and dolomite). Sustained groundwater abstraction from a lens can significantly alter the hydrochemistry of the water lens. This suggests that hydrochemical characterization of small fresh water lenses, like those on Grand Cayman, cannot be based on spot or short-term sampling. Interpretation of such fluids in terms of calcite-dolomite precipitation and/or dissolution must be treated with caution if the data base has not been derived from long-term monitoring

Geochemistry of the Springfield Plateau aquifer of the Ozark Plateaus Province in Arkansas, Kansas, Missouri and Oklahoma, USA, 2000, Adamski Jc,
Geochemical data indicate that the Springfield Plateau aquifer, a carbonate aquifer of the Ozark Plateaus Province in central USA, has two distinct hydrochemical zones. Within each hydrochemical zone, water from springs is geochemically and isotopically different than water from wells. Geochemical data indicate that spring water generally interacts less with the surrounding rock and has a shorter residence time, probably as a result of flowing along discrete fractures and solution openings, than water from wells. Water type throughout most of the aquifer was calcium bicarbonate, indicating that carbonate-rock dissolution is the primary geochemical process occurring in the aquifer. Concentrations of calcium, bicarbonate, dissolved oxygen and tritium indicate that most ground water in the aquifer recharged rapidly and is relatively young (less than 40 years). In general, field-measured properties, concentrations of many chemical constituents, and calcite saturation indices were greater in samples from the northern part of the aquifer (hydrochemical zone A) than in samples from the southern part of the aquifer (hydrochemical zone B). Factors affecting differences in the geochemical composition of ground water between the two zones are difficult to identify, but could be related to differences in chert content and possibly primary porosity, solubility of the limestone, and amount and type of cementation between zone A than in zone B. In addition, specific conductance, pH, alkalinity, concentrations of many chemical constituents and calcite saturation indices were greater in samples from wells than in samples from springs in each hydrochemical zone. In contrast, concentrations of dissolved oxygen, nitrite plus nitrate, and chloride generally were greater in samples from springs than in samples from wells. Water from springs generally flows rapidly through large conduits with minimum water-rock interactions. Water from wells flow through small fractures, which restrict how and increase water-rock interactions. As a result, springs tend to be more susceptible to surface contamination than wells. The results of this study have important implications for the geochemical and hydrogeological processes of similar carbonate aquifers in other geographical locations. Copyright (C) 2000 John Wiley & Sons, Ltd

Water quality impacts and palaeohydrogeology in the Yorkshire Chalk aquifer, UK, 2001, Elliot T, Chadha Ds, Younger Pl,
A large hydrochemical data-set for the East Yorkshire Chalk aquifer has been assessed. Controls on the distribution of water qualities reflect: water-rock interactions (affecting especially the carbonate system and associated geochemistry); effects of land-use change (especially where the aquifer is unconfined); saline intrusion and aquifer refreshening (including ion exchange effects); and overexploitation (in the semi-confined and confined zones of the aquifer). Both Sr and I prove useful indicators of groundwater esidence times, and I/Cl ratios characterize two sources of saline waters. The hydrochemical evidence clearly reveals the importance both of recent management decisions and palaeohydrogeology in determining the evolution and distribution of groundwater salinity within the artesian and confined zones of the aquifer. Waters encountered in the aquifer are identified as complex (and potentially dynamic) mixtures between recent recharge waters, modern seawater, and ancient seawater which entered the aquifer many millennia ago

Gypsum Karst in the Western Ukraine: Hydrochemistry and Solution Rates, 2001, Klimchouk A. B. , Aksem S. D.
Gypsum karst in the Western Ukraine underlies a large territory of more than 20,000 km2 and is represented by a range of stages (evolutionary types), from deep-seated through subjacent to entrenched. Correspondingly, hydrogeological settings of karst development, circulation patterns, and chemical characteristics of groundwaters differ substantially between the respective areas. Based on 1,800 analyses, the paper summarises hydrochemistry of the gypsum-hosting Miocene aquifer. Most of the sampling has been performed in conjunction with a regime study of gypsum-solution rates by means of standard tablets. This study included 53 tablet stations representing varying conditions of water-rock interaction, where 644 weight-loss measurements have been made during 1984-1992. The highest rates are characteristic of entrenched karst, although active dissolution there is localised along well-defined sinking streams with short underground courses, rare vertical-percolation paths, and the water table. Lower, but still quite substantial, rates are characteristic for subjacent and deep-seated (confined) karst. However, the overall dissolution removal is higher there, due to higher rates of flow through the gypsum and the larger area of rock/solvent contact. The results are generalised in order to derive the approximate solution rates that characterise major situations and that are suitable for modelling purposes.

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

Geochemistry of red residua underlying dolomites in karst terrains of Yunnan-Guizhou Plateau II. The mobility of rare earth elements during weathering, 2004, Ji H. B. , Wang S. J. , Ouyang Z. Y. , Zhang S. , Sun C. X. , Liu X. M. , Zhou D. Q. ,
The aim of this study is to characterize the evolution of the rare earth elements (REE) in the Pingba red residua on karst terrain of Yunnan-Guizhou Plateau. The in-situ weathering and the two-stage development of the profile had been inferred from REE criterions. The REE were significantly fractionated, and Ce was less mobilized and separated from the other REEs at the highly enriched top of the profile. This is consistent with the increase of oxidation degree in the regolith. And it is also suggested that the wet/dry climate change during chemical weathering caused Ce alternative change between enrichment and invariance in the upper regolith. Chondrite-normalized REE distribution patterns for samples from dolomites and the lower regolith are characteristic of MREE enrichment and remarkable negative Ce-anomalies patterns (similar to the convex-up REE patterns). The following processes are interpreted for the patterns in this study: (1) the accumulation of MRRE-rich minerals in dolomite dissolution, (2) water-rock interaction in the weathering front, and (3) more leaching MREE from the upper part of the profile. The latter two explanations are considered as the dominant process for the formation of the REE patterns. Samples from the soil horizon exhibit typical REE distribution patterns of the upper crust, i.e., La-N/Yb-N = 10 and Eu/Eu* = 0.65. All data indicate that the leaching process is very important for pedogenesis in this region. The experiments demonstrating that abnormal enrichment of REE at the upper regolith-bedrock interface is caused by a combination of volume change, accumulation of REE-bearing minerals, leaching of REE from the upper regolith, and water-rock interaction during rock-soil alteration processes. Our results support the conclusion that the weathering profile represents a large, continental elemental storage reservoir, whereas REE enrichment occurs under favorable conditions in terms of stable tectonics, low erosion and rapid weathering over sufficiently long time. (C) 2003 Elsevier B.V. All rights reserved

Hydrochemical variations during flood pulses in the south-west China peak cluster karst: impacts of CaCO3-H2O-CO2 interactions, 2004, Liu Z. H. , Groves C. , Yuan D. X. , Meiman J. , Jiang G. H. , He S. Y. , Li Q. A. ,
High-resolution measurements of rainfall, water level, pH, conductivity, temperature and carbonate chemistry parameters of groundwater at two adjacent locations within the peak cluster karst of the Guilin Karst Experimental Site in Guangxi Province, China, were made with different types of multiparameter sonde. The data were stored using data loggers recording with 2 min or 15 min resolution. Waters from a large, perennial spring represent the exit for the aquifer's conduit flow, and a nearby well measures water in the conduit-adjacent, fractured media. During flood pulses, the pH of the conduit flow water rises as the conductivity falls. In contrast, and at the same time, the pH of groundwater in the fractures drops, as conductivity rises. As Ca2 and HCO3- were the dominant (>90%) ions, we developed linear relationships (both r(2) > 0.91) between conductivity and those ions, respectively, and in turn calculated variations in the calcite saturation index (SIc) and CO2 partial pressure (PCO2) of water during flood pulses. Results indicate that the PCO2 of fracture water during flood periods is higher than that at lower flows, and its SIc is lower. Simultaneously, PCO2 of conduit water during the flood period is lower than that at lower flows, and its SIc also is lower. From these results we conclude that at least two key processes are controlling hydrochemical variations during flood periods: (i) dilution by precipitation and (ii) water-rock-gas interactions. To explain hydrochemical variations in the fracture water, the water-rock-gas interactions may be more important. For example, during flood periods, soil gas with high CO2 concentrations dissolves in water and enters the fracture system, the water, which in turn has become more highly undersaturated, dissolves more limestone, and the conductivity increases. Dilution of rainfall is more important in controlling hydrochemical variations of conduit water, because rainfall with higher pH (in this area apparently owing to interaction with limestone dust in the lower atmosphere) and low conductivity travels through the conduit system rapidly. These results illustrate that to understand the hydrochemical variations in karst systems, considering only water-rock interactions is not sufficient, and the variable effects of CO2 on the system should be evaluated. Consideration of water-rock-gas interactions is thus a must in understanding variations in karst hydrochemistry. Copyright (C) 2004 John Wiley Sons, Ltd

Significance and dynamics of drip water responding to rainfall in four caves of Guizhou, China, 2005, Zhou Y. C. , Wang S. J. , Xie X. N. , Luo W. J. , Li T. Y. ,
In rainy season, NaCl is adopted to trace sources of cave drip water, time scales of drip water responding to precipitation, and processes of water dynamics in four caves of Pearl watershed in Guizhou, China (Liang-feng cave in Libo, Qixing cave in Duyun, Jiangjun cave in Anshun and Xiniu cave in Zhenning). Because of the variety of karst cave surroundings, interconnections of water transporting ways, water dynamics processes etc., time scales of drip-water in four caves responding to rainfall is 0-40 d. According to the characteristics of water transport in cave roof, pathways of water movement, types of water head etc., drip water of four caves can be divided into five hydrodynamics types. The differences of time scales, and ways of water-soil and water-rock interaction during water transporting in cave roof make it difficult to correctly measure speleothem record and trace material sources. In addition, there exist great differences in water dynamic conditions among the four caves. So the interpretation of the paleoenvironment records of speleothem must be supported by the understanding of hydrodynamics conditions of different drip sites. Based on the data got from drip sites in four caves, drip conductivity accords with precipitation, which indicates that element contents in speleothem formed by drip water record the change of karst paleoenvironment. But results of multi-points study are needed to guarantee the correctness of interpretation

Hydrochemistry and solution rates in gypsum karst: case study from the Western Ukraine, 2005, Klimchouk A. B. , Aksem S. D. ,
The gypsum karst in the Western Ukraine spreads through a large territory covering more than 20,000 km(2) and is represented by a range of stages (evolutionary types), from deep-seated through subjacent to entrenched. Correspondingly, hydrogeological settings of karst development, circulation patterns and chemical characteristics of groundwaters differ substantially between the respective areas. Based on 1,800 analyses, this paper summarises hydrochemistry of the gypsum-hosting Miocene aquifer. The majority of sampling has been performed in conjunction with a study regime of gypsum solution rates by means of standard tablets. In this study, which included 53 tablet stations representing varying conditions of water-rock interaction, 644 weight-loss measurements were made over the period 1984-1992. The highest rates are characteristic of entrenched karst although active dissolution is localised along well-defined sinking streams with short underground courses, rare vertical percolation paths and the water table. Lower but still quite substantial rates are characteristic of subjacent and deep-seated (confined) karst. However, the overall dissolution removal is greater due to higher flow through the gypsum and the larger area of rock-solvent contact. The results are generalised in order to derive the approximate solution rates characterising major situations and to be suitable for modeling purposes

Strontium isotope characterization and major ion geochemistry of karst water flow, Shentou, northern China, 2006, Wang Yanxin, Guo Qinghai, Su Chunli, Ma Teng,
SummaryKarst water is the most important source of water supply for Shanxi province, northern China. The Shentou springs are representative of the 19 major karst springs at Shanxi. The total area of the Shentou karst water system is 5316 km2, the Middle Ordovician limestone being its major karst aquifer. In this study, data about the strontium isotope geochemistry and major ion hydrochemistry were analyzed to understand the flow patterns and hydrogeochemical processes of karst water at Shentou. The contour map of TDS value of karst water and that of Sr concentration are similar, showing the general tendency of increase from the northern, western and southern boundary to the discharge area. The average values of 87Sr/86Sr ratios of karst water decrease from recharge (0.7107) to discharge area (0.7102), evolving towards those of limestone hostrocks. Comparison of 87Sr/86Sr ratios with Sr content suggests that isotopic compositions of some karst water samples from the recharge and flow through area should be the result of interaction between aquifer limestone matrix and strontium-poor recharge waters of meteoric origin. However, for samples from the discharge area that are plotted above the mixing line, mixing with groundwater in the Quaternary aquifers with high 87Sr/86Sr ratios may be another factor controlling Sr isotope chemistry. Two major groundwater flow paths were discerned from hydrogeological and geochemical data. Along both flow paths, the 87Sr/86Sr ratios of karst water show a general tendency of decrease. Geochemical modeling of the major ion geochemistry of karst water using PHREEQC also indicates that the chemistry of springs should be affected by the incorporation of groundwater in Quaternary aquifer. The effect of the mixing action on the spring hydrochemistry in flow path 1 is more remarkable than that in flow path 2, according to different mixing ratios in both paths (30% in flow path 1 and 5% in flow path 2)

Evidence against the Dorag (mixing-zone) model for dolomitization along the Wisconsin arch - A case for hydrothermal diagenesis , 2006, Luczaj, J. A.

Ordovician carbonates near the Wisconsin arch represent the type locality in ancient rocks for the Dorag, or mixing-zone, model for dolomitization. Field, petrographic, and geochemical evidence suggests a genetic link between the pervasive dolomite, trace Mississippi Valley–type (MVT) minerals, and potassium (K)-silicate minerals in these rocks, which preserve a regional hydrothermal signature. Constraints were placed on the conditions of water-rock interaction using fluid-inclusion methods, cathodoluminescence and plane-light petrography, stable isotopic analyses, and organic maturity data. Homogenization temperatures of two-phase aqueous fluid inclusions in dolomite, sphalerite, and quartz range between 65 and 120°C. Freezing data suggest a Na-Ca-Mg-Cl-H2O fluid with salinities between 13 and 28 wt.% NaCl equivalent. The pervasive dolomitization of Paleozoic rocks on and adjacent to the Wisconsin arch was the result of water-rock interaction with dense brines at elevated temperatures, and it was coeval with regional trace MVT mineralization and K-silicate diagenesis. A reevaluation of the Dorag (mixing-zone) model for dolomitization, in conjunction with convincing new petrographic and geochemical evidence, has ruled out the Dorag model as the process responsible for pervasive dolomitization along the Wisconsin arch and adds to the abundant body of literature that casts serious doubt about the viability of the Dorag model in general.

John Luczaj is an assistant professor of earth science in the Department of Natural and Applied Sciences at the University of Wisconsin–Green Bay. He earned his B. S. degree in geology from the University of Wisconsin–Oshkosh. This was followed by an M.S. degree in geology from the University of Kansas. He holds a Ph.D. in geology from Johns Hopkins University in Baltimore, Maryland. His recent interests include the investigation of water-rock interaction in Paleozoic sedimentary rocks in the Michigan Basin and eastern Wisconsin. Previous research activities involve mapping subsurface uranium distributions, reflux dolomitization, and U-Pb dating of Permian Chase Group carbonates in southwestern Kansas.


Fractured hydrothermal dolomite reservoirs in the Devonian Dundee Formation of the central Michigan Basin, 2006, Luczaj J. A. , Harrison Iii. W. B. , Williams N. S.

The Middle Devonian Dundee Formation is the most prolific oilproducing unit in the Michigan Basin, with more than 375 million bbl of oil produced to date. Reservoir types in the Dundee Formation can be fracture controlled or facies controlled, and each type may have been diagenetically modified. Although fracture-controlled reservoirs produce more oil than facies-controlled reservoirs, little is known about the process by which they were formed and diagenetically modified. In parts of the Dundee, preexisting sedimentary fabrics have been strongly overprinted by medium- to coarse-grained dolomite. Dolomitized intervals contain planar and saddle dolomite, with minor calcite, anhydrite, pyrite, and uncommon fluorite. Fluid inclusion analyses of two-phase aqueous inclusions in dolomite and calcite suggest that some water-rock interaction in these rocks occurred at temperatures as high as 120–150jC in the presence of dense Na-Ca-Mg-Cl brines. These data, in conjunction with published organic maturity data and burial reconstructions, are not easily explained by a long-term burial model and have important implications for the thermal history of the Michigan Basin. The data are best explained by a model involving short-duration transport of fluids and heat from deeper parts of the basin along major fault and fracture zones connected to structures in the Precambrian basement. These data give new insight into the hydrothermal processes responsible for the formation of these reservoirs. 


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