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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 imported water is water coming from outside the ground-water basin under consideration [16].?

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


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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 mg (Keyword) returned 231 results for the whole karstbase:
Showing 226 to 231 of 231
An approach for collection of nearfield groundwater samples in submerged limestone caverns, 2013,
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Mills Aaron L. , Tysall Terrence N. , Herman Janet S.

Walls of submerged caves feeding Florida springs are often lined with a heavy mat of filamentous bacteria, many of which are able to oxidize reduced sulfur in groundwater migrating from the porous bedrock into the cave conduit. To determine changes in water chemistry as water passes through the microbial mat, a simple device made from standard well screen and sealed with a rubber stopper and controllable vents was installed in a hole drilled in the wall of the cave passage. The sampler was sealed in place with marine epoxy. we measured anions in water from the sampler and from the water-filled conduit taken just outside the sampler. Most anions measured viz., Cl, NO3, and PO43−, increased slightly between the matrix and conduit waters. However, traces of sulfide were measured in the water from the rock matrix, but not in the conduit. SO4 2−concentrations in the conduit were about twice that measured in the water from the sampler, about 22 and 11 mg SO42− L−1, respectively, providing further evidence that sulfur oxidation is an important process in the bacterial mats attached to the limestone surfaces in these caves. An additional use of the sampling device is to measure discharge from the local bedrock into the cave conduit.


Using isotopes of dissolved inorganic carbon species and water to separate sources of recharge in a cave spring, northwestern Arkansas, USA Blowing Spring Cave, 2013,
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Knierim Katherine J. , Pollock Erik, Hays Phillip D.

Blowing Spring Cave in northwestern Arkansas is representative of cave systems in the karst of the Ozark Plateaus, and stable isotopes of water (δ18O and δ2H) and inorganic carbon (δ13C) were used to quantify soil-water, bedrock-matrix water, and precipitation contributions to cave-spring flow during storm events to understand controls on cave water quality. water samples from recharge-zone soils and the cave were collected from March to May 2012 to implement a multicomponent hydrograph separation approach using δ18O and δ2H of water and dissolved inorganic carbon (δ13C–DIC). During baseflow, median δ2H and δ18O compositions were –41.6‰ and –6.2‰ for soil water and were –37.2‰ and –5.9‰ for cave water, respectively. Median DIC concentrations for soil and cave waters were 1.8 mg/L and 25.0 mg/L, respectively, and median δ 13C–DIC compositions were –19.9‰ and –14.3‰, respectively. During a March storm event, 12.2 cm of precipitation fell over 82 h and discharge increased from 0.01 to 0.59 m3 /s. The isotopic composition of precipitation varied throughout the storm event because of rainout, a change of 50‰ and 10‰ for δ2H and δ18O was observed, respectively. Although, at the spring, δ2H and δ18O only changed by approximately 3‰ and 1‰, respectively. The isotopic compositions of precipitation and pre-event (i.e., soil and bedrock matrix) water were isotopically similar and the two-component hydrograph separation was inaccurate, either overestimating (>100%) or underestimating (<0%) the precipitation contribution to the spring. During the storm event, spring DIC and δ13C–DIC de- creased to a minimum of 8.6 mg/L and –16.2‰, respectively. If the contribution from precipitation was assumed to be zero, soil water was found to contribute between 23 to 72% of the total volume of discharge. Although the assumption of negligible contributions from precipitation is unrealistic, especially in karst systems where rapid flow through conduits occurs, the hydrograph separation using inorganic carbon highlights the importance of considering vadose-zone soil water when analyzing storm chemohydrographs.  


SPELEOGENESIS BY THE SULFIDIC SPRINGS AT NORTHERN SIERRA DE CHIAPAS, MEXICO, BASED ON THEIR WATER CHEMISTRY, 2014,
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Rosaleslagarde L. , Boston P. J.

Conspicuous brackish sulfidic springs have been described at the northern Sierra the Chiapas, Mexico. These springs are produced by a mixture between regional and local groundwater flow paths. The regional groundwater has an average Total Dissolved Ions of 3081 mg/L so it has a brackish composition. This brackish water is saturated with respect to calcite and dolomite but undersaturated with respect to gypsum, anhydrite and halite. The mass balance and the discharge rate are used to quantify the mass and volume of minerals that are dissolved by the brackish spring water following Appelo and Postma (1993). This quantification will allow comparing the various speleogenetic mechanisms in the area. This is considering the composition of the spring water is relatively constant over time, as it is suggested by periodic measurements at the Cueva de Villa Luz springs during the last 10 years.
Sulfur isotopes in the water are consistent with anhydrite dissolution as the main source of the sulfate to the brackish spring water. Thus, the average 6 mol/L of sulfate in the brackish springs are produced by dissolution of 6 mol of anhydrite after subtracting the sulfate that could result from evapotranspiration of rainwater. Each liter of brackish water dissolved an average of 882 mg of anhydrite, which are equivalent to dissolving 0.36 cm3 of this mineral considering a density of 2.981 g/cm3. Additionally, using the average brackish water discharge rate of 144 L/s, an average of 57 g of anhydrite are being dissolved each second per every liter of brackish water. This is a minimal value because some of the sulfate in the water is used by sulfate-reducing bacteria in the subsurface to produce the hydrogen sulfide in the spring water. The anhydrite subject to dissolution is found interbedded in the Cretaceous carbonates, either from the subsurface at 4,000 m below sea level to the carbonate outcrops.
Similarly, we can calculate the volume of halite that is being dissolved by the brackish springs, considering chloride is a conservative element and subtracting the chloride concentration from the rainwater from that of the spring water following Appelo & Postma (1993). The 22 mol/L of chloride in the brackish water can result from dissolution in the subsurface of 22 moles or 1.3 g of halite per liter of brackish water. This mass of halite dissolved is equal to 0.59 cm3 considering a density of 2.168 g/cm3. Alternatively, 118 g of halite are dissolved per second per each liter of brackish water if we use the average discharge rate of 144 L/s.
Even when the brackish springs are oversaturated with respect to calcite and dolomite, their dissolution is still possible due to the common ion-effect of calcium after anhydrite dissolution and by mixing of waters with different compositions. A range of 10 to 80 % of brackish water from the regional aquifers mixes with fresh water from the local aquifer based on their water chemistry. Additionally, sulfuric acid speleogenesis occurs due to the oxidation of hydrogen sulfide to sulfuric acid.
Finally, the increase in the chloride concentration of the fresh water springs with respect to the concentration in rainwater was used to estimate that from the 4000 mm/y of annual precipitation, only 4%, 158 to 182 mm/y, recharge the aquifers. This low percentage is slightly higher than the 3.3% recharge in marls, marly limestone, silts and clays (Sanz et al., 2011), probably because of the relatively small area of carbonate outcrops over the entire region and the lack of recharge in altitudes higher than 1500 m above sea level.
Sulfuric acid is the most obvious speleogenetic mechanism occurring in the caves of the northern Sierra de Chiapas, Mexico due to the high hydrogen sulfide concentration in the spring water. In addition, the location of the springs at a zone of regional and local discharge where waters from different composition converge and mix, and the amount of mixing calculated suggests mixing is also an important speleogenetic mechanism. However, the depth and the time constrains at which these two hypogenic mechanisms occur is still unknown. The relatively low rainwater recharge rate suggests epigenesis is limited. Most likely, the porosity created by dissolution of anhydrite and halite in the subsurface is occluded by the precipitation of calcite. Chemical modeling and petrography will help to elucidate the order of the reactions occurring in the subsurface.


Groundwater geochemistry observations in littoral caves of Mallorca (western Mediterranean): implications for deposition of phreatic overgrowths on speleothems., 2014,
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Boop L. M. , Onac B. P. , Wynn J. G. , Fornós J. J. , Rodríguezhomar M. , Merino A.

Phreatic overgrowths on speleothems (POS) precipitate at the air-water interface in the littoral caves of Mallorca, Spain. Mainly composed of calcite, aragonite POS are also observed in specific locations. To characterize the geochemical environment of the brackish upper water column, water samples and salinity values were collected from water profiles (0-2.9 m) in April 2012 and March 2013 near aragonite POS in Cova des Pas de Vallgornera and calcite POS in Coves del Drac (hereafter, Vallgornera and Drac). Degassing of CO2 from the water was evidenced by the existence of lower dissolved inorganic carbon (DIC) concentration and enriched δ13CDIC values in a thin surface layer (the uppermost 0.4 m), which was observed in both profiles from Drac. This process is facilitated by the efficient exchange of cave air with the atmosphere, creating a CO2 partial pressure (pCO2) disparity between the cave water and air, resulting in the precipitation of calcite POS as CO2 degasses from the water. The degassed upper layer was not observed in either profile from Vallgornera, suggesting that less efficient cave ventilation restricts outgassing of CO2, which also results in accumulation of CO2 in the cave atmosphere. The presence of an existing uncorroded POS horizon, as well as higher concentrations and large amplitude fluctuations of cave air pCO2, may indicate that aragonite POS deposition is currently episodic in Vallgornera. Ion concentration data from monthly water samples collected in each cave between October 2012 and March 2013 indicate higher Mg:Ca, Sr:Ca, Ba:Ca and Sr:Mg ratios in Vallgornera. Salinity alone does not appear to be a viable proxy for ions that may promote aragonite precipitation or inhibit calcite precipitation. Instead, these ions may be contributed by more intense bedrock weathering or deep groundwater flow.


Sulphuric acid speleogenesis and landscape evolution: Montecchio cave, Albegna river valley (Southern Tuscany, Italy), 2014,
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Piccini L. : Dewaele J. , Galli E. , Polyak V. J. , Bernasconi S. M. , Asmerom Y.

Montecchio cave (Grosseto province, Tuscany, Italy) opens at 320 m asl, in a small outcrop of Jurassic limestone (Calcare Massiccio Fm.), close to the Albegna river. This area is characterised by the presence of several thermal springs and the outcropping of travertine deposits at different altitudes. The Montecchio cave, with passage length development of over 1700 m, is characterised by the presence of several sub-horizontal passages and many medium- and small-scale morphologies indicative of sulphuric acid speleogenesis (SAS). The thermal aquifer is intercepted at a depth of about 100 m below the entrance: the water temperature exceeds 30 °C and sulphate content is over 1300mg l−1. The cave hosts large gypsumdeposits from40 to 100mbelowthe entrance that are by-products of the reaction between sulphuric acid and the carbonate host rock. The lower part of the cave hosts over 1 m thick calcite cave raft deposits, which are evidence of long-standing, probably thermal, water in an evaporative environment related to significant air currents. Sulphur isotopes of gypsumhave negative δ34S values (from−28.3 to−24.2‰), typical of SAS. Calcite cave rafts and speleogenetic gypsumboth yield young U/Th ages varying from68.5 ka to 2 ka BP, indicating a rapid phase of dewatering followed by gypsumprecipitation in aerate environment. This fastwater table lowering is related to a rapid incision of the nearby Albegna river, andwas followed by a 20–30mfluctuation of the thermalwater table, as recorded in the calcite raft deposits and gypsum crusts.


Sulphuric acid speleogenesis and landscape evolution: Montecchio cave, Albegna river valley (Southern Tuscany, Italy), 2015,
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Piccini Leonardo, De Waele Jo, Galli Ermanno, Polyak Victor J. , Bernasconi Stefano M. Asmerom Yemane

Montecchio cave (Grosseto province, Tuscany, Italy) opens at 320 m asl, in a small outcrop of Jurassic limestone (Calcare Massiccio Fm.), close to the Albegna river. This area is characterised by the presence of several thermal springs and the outcropping of travertine deposits at different altitudes. The Montecchio cave, with passage length development of over 1700 m, is characterised by the presence of several sub-horizontal passages and many medium- and small-scale morphologies indicative of sulphuric acid speleogenesis (SAS). The thermal aquifer is intercepted at a depth of about 100 m below the entrance: the water temperature exceeds 30 °C and sulphate content is over 1300 mg l−1. The cave hosts large gypsumdeposits from40 to 100mbelowthe entrance that are by-products of the reaction between sulphuric acid and the carbonate host rock. The lower part of the cave hosts over 1 m thick calcite cave raft deposits, which are evidence of long-standing, probably thermal, water in an evaporative environment related to significant air currents.

Sulphur isotopes of gypsum have negative δ34S values (from−28.3 to−24.2‰), typical of SAS. Calcite cave rafts and speleogenetic gypsumboth yield young U/Th ages varying from68.5 ka to 2 ka BP, indicating a rapid phase of dewatering followed by gypsum precipitation in aerate environment. This fastwater table lowering is related to a rapid incision of the nearby Albegna river, and was followed by a 20–30 m fluctuation of the thermal water table, as recorded in the calcite raft deposits and gypsum crusts.


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