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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 covered karren is any karren that is covered by soil. draining water is oversaturated with respect to co2 so that corrosion is extensive [3]. see also wave karren; root karren; cavernous karren.?

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

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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.
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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 sea-water (Keyword) returned 21 results for the whole karstbase:
Showing 1 to 15 of 21
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

Palaeogeographic environment during the desiccation of the Black Sea, 1983, Kojumdgieva Emilia,
During the latest Chersonian (about 10.3 m.y. ago) tectonic movements took place leading to an elevation of the Crimean-Caucasian chain and to an isolation of the Fore-Caucasian part of the Black Sea Basin. This part of the basin had been draining the rivers of the Russian Platform and after the isolation it became desalinized, while the main part of the Black Sea Basin was almost desiccated and evaporites, mainly dolomites, formed in it due to the predominant calcium---magnesium---carbonate composition of the Chersonian Sea waters. These dolomites are found in the drillings of DSDP Leg 42B and are confirmed geophysically.The tectonic movements during the latest Chersonian led to the formation of a series of grabens along which the Mediterranean Sea invaded the north Aegean area and a little later (during the Early Maeotian) the Black Sea

Regional dolomitization of subtidal shelf carbonates: Burlington and Keokuk Formations (Mississippian), Iowa and Illinois, 1987, Harris David C. , Meyers William J. ,
Cathodoluminescent petrography of crinoidal limestones and dolomites from the Mississippian (Osagean) Burlington and Keokuk Formations in Iowa and Illinois has revealed a complex diagenetic history of calcite cementation, dolomitization, chertification and compaction. Dolomite occurs abundantly in subtidal, open-marine facies throughout the study area. Three luminescently and chemically distinct generations of dolomite can be recognized regionally. Dolomite I, the oldest generation, is luminescent, thinly zoned, and occurs mainly as a replacement of lime mud. Dolomite II has dull red unzoned luminescence, and occurs mainly as a replacement of dolomite I rhombs. Dolomite III is non-luminescent, and occurs as a syntaxial cement on, and replacement of, older dolomite I and II rhombs. Petrography of these dolomite generations, integrating calcite cement stratigraphy, chertification and compaction histories has established the diagenetic sequence. Dolomites I and II pre-date all calcite cements, most chert, intergranular compaction and styloites. Dolomite III precipitation occurred within the calcite cement sequence, after all chert, and after at least some stylolitization. The stratigraphic limit of these dolomites to rocks older than the St Louis Limestone (Meramecian) suggests that dolomitization took place before or during a regional mid-Meramecian subaerial unconformity. A single dolomitization model cannot reasonably explain all three generations of dolomite in the Burlington and Keokuk limestones. Petrographic and geochemical characteristics coupled with timing constraints suggest that dolomite I formed in a sea water-fresh water mixing zone associated with a meteoric groundwater system established beneath the pre-St Louis unconformity. Dolomite II and III may have formed from externally sourced warm brines that replaced precursor dolomite at shallow burial depths. These models therefore suggest that the required Mg for dolomite I was derived mainly from sea water, whereas that for dolomites II and III was derived mainly from precursor Burlington--Keokuk dolomites through replacement or pressure solution

Chemical hydrogeology in natural and contaminated environments, 1989, Back W, Baedecker Mj,
Chemical hydrogeology, including organic and inorganic aspects, has contributed to an increased understanding of groundwater flow systems, geologic processes, and stressed environments. Most of the basic principles of inorganic-chemical hydrogeology were first established by investigations of organic-free, regional-scale systems for which simplifying assumptions could be made. The problems of groundwater contamination are causing a shift of emphasis to microscale systems that are dominated by organic-chemical reactions and that are providing an impetus for the study of naturally occurring and manmade organic material. Along with the decrease in scale, physical and chemical heterogeneity become major controls.Current investigations and those selected from the literature demonstrate that heterogeneity increases in importance as the study site decreases from regional-scale to macroscale to microscale. Increased understanding of regional-scale flow systems is demonstrated by selection of investigations of carbonate and volcanic aquifers to show how application of present-day concepts and techniques can identify controlling chemical reactions and determine their rates; identify groundwater flow paths and determine flow velocity; and determine aquifer characteristics. The role of chemical hydrogeology in understanding geologic processes of macroscale systems is exemplified by selection of investigations in coastal aquifers. Phenomena associated with the mixing zone generated by encroaching sea water include an increase in heterogeneity of permeability, diagenesis of minerals, and formation of geomorphic features, such as caves, lagoons, and bays. Ore deposits of manganese and uranium, along with a simulation model of ore-forming fluids, demonstrate the influence of heterogeneity and of organic compounds on geochemical reactions associated with genesis of mineral deposits. In microscale environments, importance of heterogeneity and consequences of organic reactions in determining the distributions and concentrations cf. constituents are provided by several studies, including infiltration of sewage effluent and migration of creosote in coastal plain aquifers. These studies show that heterogeneity and the dominance of organically controlled reactions greatly increase the complexity of investigations

Limestone caves form along ground-water paths of greatest discharge and solutional aggressiveness. Flow routes that acquire increasing discharge accelerate in growth, while others languish with negligible growth. As discharge increases, a maximum rate of wall retreat is approached, typically about 0.01-0.1 cm/yr, determined by chemical kinetics but nearly unaffected by further increase in discharge. The time required to reach the maximum rate is nearly independent of kinetics and varies directly with flow distance and temperature and inversely with initial fracture width, discharge, gradient, and P(CO2). Most caves require 10(4) - 10(5) yr to reach traversable size. Their patterns depend on the mode of ground-water recharge. Sinkhole recharge forms branching caves with tributaries that join downstream as higher-order passages. Maze caves form where (1) steep gradients and great undersaturation allow many alternate paths to enlarge at similar rates or (2) discharge or renewal of undersaturation is uniform along many alternate routes. Flood water can form angular networks in fractured rock, anastomotic mazes along low-angle partings, or spongework where intergranular pores are dominant. Diffuse recharge also forms networks and spongework, often aided by mixing of chemically different waters. Ramiform caves, with sequential outward branches, are formed mainly by rising thermal or H2S-rich water. Dissolution rates in cooling water increase with discharge, CO2 content, temperature, and thermal gradient, but only at thermal gradients of more than 0.01-degrees-C/m can normal ground-water CO2 form caves without the aid of hypogenic acids or mixing. Artesian flow has no inherent tendency to form maze caves. Geologic structure and stratigraphy influence cave orientation and extent, but alone they do not determine branch-work versus maze character

From a geographical point of view, the atoll of Mururoa belongs to the Tuamotu archipelago. In its largest dimension Mururoa (28 x 10 km) is oriented N080-degrees-E, a direction which is different from that of the other atolls of the Tuamotu, generally oriented parallel to the Pacific plate motion, N130-degrees-E. The atoll of Mururoa is built on a submarine plateau of 130 km long and 30 km wide. The western side of this plateau is 90 km long and N080-degrees-E oriented, the eastern one 40 km long and N095-degrees-E oriented. Three deep main structures of the atoll are revealed by strong aeromagnetic anomalies elongated and oriented once more N080-degrees-E. They represent ancient riftzones, similar to the present time Hawaiian ones. The most important of them, situated at southern end of the atoll, is the prolongation of the eastern plateau. The principal petrographic facies have been defined from the numerous drill holes bored in the upper 1,100 m. From the base to the top are represented volcanic deposits, a volcano-sedimentary serie of both carbonate and volcanic origin and finally reefal carbonates (limestones and dolomites). The volcanic facies represent successively submarine, transitional and aerial volcanic activity. They are commonly affected by early stage of hydrothermalism, due to lava-sea-water chemical interaction, and are frequently supported by differentiated dykes, occasionally interrupted by reefal limestones. The main geometrical distribution of the facies through the atoll and the radiochronology lead to the following model of formation : during early stages of the atoll building two main separate edifices emerged before joining and forming a single volcano. This double structure was similar to the present time morphology of Tahiti. The volcanic activity ceased 10.6 Ma ago, an age which perfectly suits a hot spot origin, at present located to the south-east of Pitcairn island

Dissolution of carbonate minerals in the coastal halocline is taking place in the karst terrain along the northeastern coast of the Yucatan Peninsula. The dissolution is being accelerated in cenotes (sinkholes) where sulfate reduction and oxidation of the produced sulfide is occurring. Hydrogen-sulfide concentrations ranged from 0.06 to 4 mmolal within the halocline in two sinkholes. Relative to concentrations expected by conservative mixing, fluids with high hydrogen-sulfide concentrations were correlated with low sulfate concentrations, high alkalinities, low pH values, and heavy sulfur isotope values for sulfate. Hydrogen-sulfide concentrations were less than those predicted from sulfate reduction, calculated from deficiencies in measured sulfate concentrations, indicating mobility and loss of aqueous sulfide. Fluids with low hydrogen-sulfide concentrations were correlated with very high calcium concentrations, high strontium and sulfate concentrations, slightly elevated alkalinities, low pH values, and sea-water sulfur isotope values for sulfate. Gypsum dissolution is supported by the sulfur isotopes as the major process producing high sulfate concentrations. However, oxidation of aqueous sulfide to sulfuric acid, resulting in carbonate-mineral dissolution is needed to explain the calcium concentrations, low pH values, and only slightly elevated alkalinities. The halocline may trap hydrogen sulfide that has been stripped from the underlying anoxic salt water. The halocline can act as a stable, physical boundary, holding some of the hydrogen sulfide until it is oxidized back to sulfuric acid through interaction with the overlying, oxygenated fresh water or through the activity of sulfide-oxidizing bacteria

Marine carbonate cements, which are superficially like travertines from meteoric caves, are coating and binding some intertidal sedimentary rock surfaces occurring in coastal Abu Dhabi, the United Arab Emirates, (UAE). Near Jebel Dhana these surficial cements can be up to 3 cm thick and envelope beach rock surfaces and fossils. They are also present both as thin coats and a fracture-fill cement in the intertidal hard grounds associated with the Khor Al Bazam algal flats. The thickness, microscopic characteristics, and morphology of the marine cement coatings from Jebel Dhana indicates incremental deposition of aragonite in conjunction with traces of sulfate minerals. Most of these cement coatings are micritic, but the layers which encrust the hard grounds from the algae flat of the Khor al Bazam have a more radial and fibrous micro-structure and are composed solely of aragonite. The stable isotopic composition of coatings from Jebel Dhana (delta(18)O = .35, delta(13)C = .00) falls within the compositional range for modem marine non skeletal aragonite and suggests that the marine travertine-like cements precipitate from the agitated slightly hypersaline Arabian Gulf sea water during repeated cycles of exposure, evaporation and immersion. Similar cement coatings and microfabrics are present in the tepee structured and brecciated sediments of the Guadalupe Mountains (Permian) and the Italian Alps (Triassic), in Holocene algal head cements from the Great Salt Lace, and in similar Tertiary algal heads in the Green River Formation of the western US. The petrographic similarity of these ancient ''flow stone'' like cements with Recent hypersaline marine cement coatings suggests that high rates of carbonate cementation and hypersaline conditions contribute to tepee formation and cavity fill

The Wilde Kirche reef complex (Early-Late Rhaetian) grew as an isolated carbonate structure within the shallow Kossen Basin. At the Triassic/Jurassic boundary a single brief(c. 10-50 ka) period of subaerial exposure occurred. The preserved karst profile (70 m thick) displays a vadose zone, enhanced dissolution at a possible palaeo-watertable (5-15m below the exposure surface), and a freshwater phreatic zone. Karst porosity was predominantly biomouldic. primary cavities and biomoulds were enlarged and interconnected in the freshwater phreatic zone; cavity networks developed preferentially in patch reef facies. Resubmegence of the reef complex allowed minor modification of the palaeokarst surface by sea floor dissolution and Fe-Mn crust deposition on a sediment-starved passive margin. Fibrous calcite (FC), radiaxial fibrous calcite (RFC) and fascicular optic calcite (FOC) cements preserved as low Mg calcite (LMC) are abundant in primary and karst dissolution cavities. FC cement is restricted to primary porosity, particularly as a synsedimentary cement at the windward reef margin. FC, RFC and FOC contain microdolomite inclusions and show patchy non-/bright cathodoluminescence. delta(18)O values ofnon-luminescent portions (interpreted as near original) are -1.16 to -1.82 parts per thousand (close to the inferred delta(18)O of calcite precipitated from Late Triassic sea water). delta(13)C values are constant ( to .2 parts per thousand). These observations suggest FC, RFC and FOC were originally marine high Mg calcite (HMC) precipitates, and that the bulk of porosity occlusion occurred not in the karst environment but in the marine environment during and after marine transgression. The HMC to LMC transition may have occurred in contact with meteoric water only in the case of FC cement. The most altered (brightly luminescent) portions of RFC/FOC cements yield delta(18)O = -2.44 to -5.8 parts per thousand, suggesting HMC to LMC alteration at up to 34 degrees C, in the shallow burial environment at depths of 180-250 m. Abundant equant cements with delta(18)O = -4.1 to -7.1 parts per thousand show crisp, uniform or zoned dull luminescence. They are interpreted as unaltered cements precipitated at 33-36 degrees C at 200-290 m burial depth, from marine-derived fluids under a slightly enhanced geothermal gradient. Fluids carrying the equant cements may have induced the HMC to LMC transition in the fibrous cements

A range of hydrodynamic dispersion coefficients was estimated for fracture-fluid and combined fracture and pore-fluid now within the halocline of the limestone aquifer forming the surface of the northern Yucatan Peninsula. The coefficients are fit parameters in a model reproducing observed halocline profiles in a sinkhole and in a borehole near the northeastern coast. Fitted coefficients range from 10(-7) to 10(-4) cm(2)/sec, of which molecular diffusion, without transverse (vertical) dispersion, can account for 10(-7) to 10(-5) cm(2)/sec. The mechanical stability of the vertical density gradient in the halocline dampens transverse dispersion in pore fluids and in fracture fluids that are transitional between laminar and turbulent flow. The dampening is proportional to the ratio of the energy needed for the fluid to rise and displace a less dense fluid to the vertical component of the kinetic energy of the fluid. The ratio of these two energies is at a maximum during the initial stage of development of a halocline and decreases as the halocline widens

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 and water dynamics: Application to short time-scale flood phenomena in a small Mediterranean catchment .1. Alkalis, alkali-earths and Sr isotopes, 1997, Benothman D, Luck Jm, Tournoud Mg,
We report major, trace elements and Sr isotope data for water samples taken regularly during a four-day-long September flood of a Mediterranean river, the Vene (Herault, S. France). The objective is to combine all these data into a dynamic model that describes the origin(s) and movements of waters and their loads. This river drains the runoff from a small, mainly carbonate, partly karstified watershed with Miocene and Jurassic lithologies. The watershed is also impacted by both agricultural and urban activities. Both the dissolved and the particulate loads were analyzed. Concentrations of the dissolved components show major remobilization of almost all elements during the first few hours of the flood (water treatment plants and aerosol scavenging), followed by a sharp concentration decrease. Some major species return to their previous summer values (Ca, HCO3) while others reach low 'background' levels (Na, K, Cl, SO4). Some trace elements (Rb, Sr, Cs) show similar behaviour but (Ba) appears somewhat unaffected. Trace element concentrations and ratios define two main periods (three in the suspended particulate matter). Ratios do not allow distinguishing between the three main sources for the dissolved load in the first period (Miocene, Jurassic, water treatment plants), but clearly show the Jurassic karst influence later on. The Sr-87/Sr-86 Of the suspended particulate matter is more variable and more radiogenic than in the dissolved phase. Variations in concentration ratios and Sr isotope composition in particulates indicate the large and variable contribution of Miocene silicates with some carbonate. However, there is a need for another component with [Rb]/[Sr] higher than bedrocks, internal or external to the watershed, possibly due to differential erosion. Dissolved Ca and Mg fluxes during the flood were calculated at 0.26 ton and 0.029 ton/km(2), respectively. Even though the carbonate nature of the watershed restricts variability in Sr isotope composition in the dissolved load, we distinguish several endmembers: seawater(approximate to marine rain), Miocene marls, Jurassic limestones, water treatment plants (and possibly another attributable to fertilizers). Combined with major and trace element variational Sr isotope fluctuations indicate time-varying proportions of different water endmembers at the outflow and suggest a general dynamic model. Based on PCA (principal component analysis), a 3D representation allows to visualize the geochemical evolution of the Vene waters. In particular, Sr isotopes clearly indicate that the inflow of karstic waters during the flood was not continuous but occurred as a series of marked oscillations between flowing waters with chemical signature of Miocene lithologies and increasing flushes of deeper waters that interacted with Jurassic lithologies. (C) 1997 Elsevier Science B.V

Sea water intrusion in coastal karst springs: Example of the Blaz spring (Croatia), 1997, Bonacci O, Rojebonacci T,
Brackish karst springs are common along every karstic sea shore consisting of limestone and dolomite. On the Croatian sea coast there are more than 300 permanent or temporary brackish karst springs. From the standpoint of water supply, the problem of karst spring water salinization is quite significant because large quantities of high quality fresh water are not available to be used either as drinking water or for industrial and agricultural purposes. The salinity of brackish karst springs situated along the Adriatic coast varies from 10 to more than 18 000 mg Cl 1(-1) with an unfavourable distribution during the year. In the wet winter period, when water quantities in the region are abundant, the salinity is exceedingly low. In the warm and dry summer period the chloride concentration is high. At that season, when a shortage of flesh water in the region occurs, especially due to tourism, karst spring water is so salty that it cannot be used at all. The mechanism of sea water intrusion is relatively well known but the problem of karst springs desalinization has not been solved in practice. The Ghyben-Herzberg relationship is formulated exclusively on the basis of hydrostatic equilibrium, and its use under dynamic conditions is limited. The dynamics of fresh water circulation towards karst spring exits are very specific for each individual spring. Using numerous hydrological, hydrometric, hydrogeological and speleological investigations of the brackish Blaz (Croatia) karst spring, this paper gives the plausible position and dimensions of the main karst conduits through which sea water penetrates into the spring exit

Geological factors affecting the chemical characteristics of the thermal waters of the carbonate karstified aquifers of Northern Vietnam, 2000, Drogue C, Cat Nn, Dazy J,
In northern Vietnam, exposed carbonate rock formations cover an area of more than 50,000 km(2). Their accumulated thickness from the Cambrian to the Triassic is in some places as much as 3000 m. Numerous thermal waters (springs and wells) occur in these strongly karstified carbonate massifs. This is the result of significant ancient and present orogenic activity, as the region demonstrates by its strong seismic activity. These karstic formations are water-bearing and strongly recharged by rainfall of between 1600 mm and 2600 mm per year in 90% of the area concerned. In view of the average annual air temperatures ( 17 degreesC-25 degreesC according to the region), 23 sample springs or wells were chosen with water temperatures of between 29 degreesC and 68 degreesC. Hydrochemical characteristics of these thermal waters emerging in different carbonate-rock units were examined by chemical analyses of major ions. In this large region, thermal waters are divided into four hydrochemical types: the Na-Cl type resulting from the intrusion of sea water for distances of up to several kilometres inland and depths of 1000 m, the Ca-SO4 type, probably resulting from the leaching of deposits of metallic sulphides that are widely distributed in these carbonate-rock units, and finally the Ca-HCO3 and Mg-HCO3 types which are chemically similar to fresh karstic waters in limestones and dolostones. The occurrence of these thermal groundwaters as well as their chemical characteristics seem to indicate the existence of large-scale deepseated groundwater flow systems in the karstic aquifers

Diagenetic History of Pipe Creek Jr. Reef, Silurian, North-Central Indiana, U.S.A, 2000, Simo J. A. , Lehmann Patrick J. ,
Calcite cements in the Silurian (Ludlovian) Pipe Creek Jr. Reef, north-central Indiana, are compositionally zoned with characteristic minor-element concentrations and stable-isotope signatures, and were precipitated in different diagenetic environments. Superposition and crosscutting relationships allow us to group cement zones and to relate them to the sequence stratigraphic evolution of the reef. Pipe Creek Jr. Reef grew in normal marine waters, with the reef top high (greater than 50 m) above the platform floor. Flank facies are volumetrically important and are preserved largely as limestone, in contrast to most dolomitized Silurian reefs in the midcontinent. Syndepositional marine cements fill primary porosity and synsedimentary fractures and are interlayered with marine internal sediment. Now low-magnesium calcite, their isotopic compositions are similar to those of depositional grains and cements estimated to have precipitated from Ludlovian sea waters. Depositional porosity was reduced by 75% by the precipitation of these syndepositional cements, which stabilized the steeply dipping flank slope. Postdepositional, clear calcite cements are interpreted as shallow-phreatic and burial cements on the basis of their relationship to periods of karstification and fracturing. Shallow-phreatic cements, with concentric cathodoluminescent (CL) zonation, precipitated in primary pores and are postdated by fractures and caves filled with Middle Devonian sandstone. CL zonal boundaries are sharp, and some, near a major stratigraphic unconformity, show evidence of dissolution. The volumetric abundance of the individual CL zones varies in the reef, indicating a complex superposition of waters of varying chemistry and rock-water interaction that are probably related to relative sea-level changes. This important aspect of the reef stratigraphy is recorded only by the diagenetic succession, because evidence of earlier sea-level changes is removed by a major later regional unconformity. Burial cements are the youngest diagenetic feature recognized, and they rest conformably or unconformably over older cements. They exhibit both concentric CL zonation and sectoral zoning, they are ferroan to nonferroan, and they contain thin sulfide zones along growth-band boundaries. Their isotopic compositions do not overlap with shallow-phreatic or marine cement values. Degraded oil postdates burial cements, and is composed of the same sterane class as the Devonian-age Antrim Shale, the probable source rock. This source contrasts with that of reef reservoirs in the Michigan Basin, where Silurian strata are commonly the hydrocarbon source

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