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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 glacier cave is 1. a cave carved out of the ice inside a glacier, not to be confused with an ice cave. passages are formed by meltwater descending from the glacier surface via crevasses, or by melting on the glacier base. through caves may connect sinkholes (sometimes called moulins) to glacier snout resurgences, but due to ice movement most glacier caves are ephemeral. the most extensively explored glacier caves were the paradise caves on mount rainier, usa, whose passages extended for many kilometers, before the glacier wasted away and the caves were destroyed [9]. 2. cave in ice formed within or at the base of a glacier [10].?

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

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KarstBase a bibliography database in karst and cave science.

Featured articles from Cave & Karst Science Journals
Chemistry and Karst, White, William B.
Engineering challenges in Karst, Stevanović, Zoran; Milanović, Petar
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Featured articles from other Geoscience Journals
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 chemical-composition (Keyword) returned 25 results for the whole karstbase:
Showing 1 to 15 of 25
Mixing corrosion in CaCO3/1bCO2/1bH2O systems and its role in the karstification of limestone areas, 1981, Dreybrodt W,
Mixtures of two saturated H2O/1bCO2/1bCaCO3 solutions of different chemical composition gain renewed capability of dissolving calcite. This is an important mechanism in the solution processes of limestone during karstification. Using recent data on the kinetics of calcite dissolution, dissolution rates in mixture corrosion are calculated. In the region of the chemical composition of natural karst waters the solution rate is approximated by:R=-[alpha]([Ca2] - [Ca2]s where [Ca2], [Ca2]s are the concentrations of the Ca2 ion in the solution and at saturation, respectively. [alpha] ranges from 10-4 to 3[middle dot]10-4 cm s-1.This result is applied to the solution of limestone in karst water mixtures flowing in cylindrical conduits. The saturation length, i.e. the length xs which the solution has to travel to drop to 37% of its renewed dissolving capability, is calculated in the region of turbulent flow. This region starts at conduit radii R of several millimeters. At the onset of turbulent flow the saturation length is 260 m, increasing with R1.665. The increase of conduit radii is calculated from the dissolution rates of calcite solution to be on the order of 10-3 cm yr.-1.The results are discussed for a comprehensive model of karstification and cave development, which for the first time gives a realistic theoretical time region for cave development, in agreement to experience

C-14 activity of dissolved inorganic carbon (DIC) in water and in recent tufa samples in several karst areas of Yugoslavia and Czechoslovakia was measured. Groundwater from 11 karst springs were measured for their isotopic content (C-14, H-3, C-13), chemical composition (HCO3, Ca2, Mg2) and physico-chemical properties (temperature, pH). Seasonal variations of the C-14 activity of DIC in two karst springs in Plitvice Lakes area, Yugoslavia, were measured systematically from 1979-1987. C-14 activity of recent tufa samples from several locations downstream were also measured. The activity of DIC in karst spring water in both countries ranged from 63-87 pMC, which is attributed to differences in geologic structure of the recharge area, topsoil thickness and composition. Grouping of C-14 activities of DIC ca (824)% is evident. Tritium activity at all the springs indicated short mean residence time (1-10 yr). Concentration of HCO3, Ca2 and Mg2 in spring water varied with geomorphology. C-14 activity of streamwater and recent tufa increased downstream from karst springs due to the exchange between atmospheric CO2 and DIC

Specific chemical composition of karst groundwater in the Ophiolite Belt of the Yugoslav Inner Dinarides: A case for covered karst, 1990, Kresic Neven, Papic Petar,

Hydrochemical and hydrodynamical investigations are presented to explain tufa deposition rates along the flow path of the Huanglong Ravine, located in northwestern Sichuan province, China, on an altitude of about 3400 m asl. Due to outgassing of CO2 the mainly spring-fed stream exhibits, along a valley of 3.5 km, calcite precipitation rates up to a few mm/year. We have carried out in situ experiments to measure calcite deposition rates at rimstone dams, inside of pools and in the stream-bed. Simultaneously, the downstream evolution of water chemistry was investigated at nine locations with respect to Ca2 Mg2, Na, Cl-, SO42-, and alkalinity. Temperature, pH, and conductivity were measured in situ, while total hardness, Ca-T, and alkalinity have been determined immediately after sampling, performing standard titration methods. The water turned out to be of an almost pure Ca-Mg-HCO3 type. The degassing of CO2 causes high supersaturation with respect to calcite and due to calcite precipitation the Ca2 concentration decreases from 6 . 10(-3) mole/l upstream down to 2.5 . 10(-3) mole/l at the lower course. Small rectangular shaped tablets of pure marble were mounted under different flow regimes, i.e., at the dam sites with fast water flow as well as inside pools with still water. After the substrate samples had stayed in the water for a period of a few days, the deposition rates were measured by weight increase, up to several tens of milligrams. Although there were no differences in hydrochemistry, deposition rates in fast flowing water were higher by as much as a factor of four compared to still water, indicating a strong influence of hydrodynamics. While upstream rates amounted up to 5 mm/year, lower rates of about 1 mm/year were observed downstream. Inspection of the marble substrate surfaces by EDAX and SEM (scanning electron microscope) revealed authigeneously grown calcite crystals of about 10 mu m. Their shape and habit are indicative of a chemically controlled inorganic origin. By applying a mass transfer model for calcite precipitation taking into account the reaction rates at the surface given by Plummer et al. (1978), slow conversion of CO2 into H and HCO3-, and diffusional mass transport across a diffusion boundary layer, we have calculated the deposition rates from the hydrochemistry of the corresponding locations. The calculated rates agree within a factor of two with the experimental results. Our findings confirm former conclusions with respect to fast flow conditions: reasonable rates of calcite precipitation can be estimated in reducing the PWP-rate calculated from the chemical composition of the water by a factor of about ten, thus correcting for the influence of the diffusion boundary layer

The kinetics of the reaction CO2?>H? as one of the rate limiting steps for the dissolution of calcite in the system H2O-CO2-CaCO3, 1996, Dreybrodt W, Lauckner J, Liu Zh, Svensson U, Buhmann D,
Dissolution of CaCO3 in the system H2O-CO2-CaCO3 is controlled by three rate-determining processes: The kinetics of dissolution at the mineral surface, mass transport by diffusion, and the slow kinetics of the reaction H2O CO2 = H HCO3-. A theoretical model of Buhmann and Dreybrodt (1985a,b) predicts that the dissolution rates depend critically on the ratio V/A of the volume V of the solution and the surface area A of the reacting mineral. Experimental data verifying these predictions for stagnant solutions have been already obtained in the range 0.01 cm < V/A < 0.1 cm. We have performed measurements of dissolution rates in a porous medium of sized CaCO3 particles for V/A in the range of 2 . 10(-4) cm and 0.01 cm in a system closed with respect to CO2 using solutions pre-equilibrated with an initial partial pressure of CO2 of 1 . 10(-2) and 5 . 10(-2) atm. The results are in satisfactory agreement with the theoretical predictions and show that especially for V/A < 10(-3) cm dissolution is controlled entirely by conversion of CO2 into H and HCO3-, whereas in the range from 10(-3) cm up to 10(-1) cm both CO2-conversion and molecular diffusion are the rate controlling processes. This is corroborated by performing dissolution experiments using 0.6 mu molar solutions of carbonic anhydrase, an enzyme enhancing the CO2-conversion rates by several orders of magnitude. In these experiments CO2 conversion is no longer rate limiting and consequently the dissolution rates of CaCO3 increase significantly. We have also performed batch experiments at various initial pressures of CO2 by stirring sized calcite particles in a solution with V/A = 0.6 cm and V/A = 0.038 cm. These data also clearly show the influence of CO2-conversion on the dissolution rates. In all experiments inhibition of dissolution occurs close to equilibrium. Therefore, the theoretical predictions are valid for concentrations c less than or equal to 0.9 c(eq). Summarising we find good agreement between experimental and theoretically predicted dissolution rates. Therefore, the theoretical model can be used with confidence to find reliable dissolution rates from the chemical composition of a solution for a wide field of geological applications

Precipitation and alteration of late Cretaceous sedimentary apatites and siderites (Leonie Trough, Bavaria, Germany), 1998, Sattler C. D. , Halbach P. ,
Late Cretaceous sedimentary siderites and fluorapatites of the iron ore deposit 'Leonie' (Bavaria, Germany) have been investigated by geochemical and mineralogical methods to define their origin. The siderites consist to more than 90 mol% of FeCO3. This elemental composition relates to an early diagenetic fresh water depositional environment. The stable isotope geochemistry of carbon and oxygen (delta(18)O: parts per thousand SMOW; delta(13)C: -12 parts per thousand PDB) also supports a siderite genesis in meteoric waters, with carbon originating from oxidation of organic matter. The chemical composition of the fluorapatites is relatively pure and shows a very low elemental substitution for calcium and phosphate. This is the result of an intense epigenetic alteration of the primary carbonate fluorapatite and, thus, cannot be related to specific source aspects. Microscopic investigations and thermodynamic calculations reveal a precursory apatite precipitation before siderite was formed. This process is thought to have removed calcium from karst waters to a level which enables siderite to be precipitated. Because of the data and observations a siderite formation in a stagnant fresh water basin is postulated, while the apatite formation probably was initiated during a connection to the open ocean (Tethys) with temporary marine ingressions. The input of iron and partly of phosphorus and fluorine into the karst basins resulted from the draining of the uplifted easterly mountains of the igneous Bohemian Massif under the influence of a humid warm climate. During the postulated marine ingressions especially phosphorus and fluorine were brought into the system whereas most of the calcium and carbonate reached the karst troughs by dissolution of the Late Jurassic Maim limestones

A new device for collecting time-integrated water samples from springs and surface water bodies, 1998, Panno S. V. , Krapac I. G. , Keefer D. A. ,
A new device termed the 'seepage sampler' was developed to collect representative water samples from springs, streams, and other surface-water bodies. The sampler collects composite, time-integrated water samples over short (hours) or extended (weeks) periods without causing significant changes to the chemical composition of the samples. The water sample within the sampler remains at the ambient temperature of the water body and does not need to be cooled. Seepage samplers are inexpensive to construct and easy to use. A sampling program of numerous springs and/or streams can be designed at a relatively low cost through the use of these samplers. Transient solutes migrating through such flow systems, potentially unnoticed by periodic sampling, may be detected. In addition, the mass loading of solutes (e.g., agrichemicals) may be determined when seepage samplers are used in conjunction with discharge measurements

Changes in the isotopic and chemical composition of ground water resulting from a recharge pulse from a sinking stream, 1998, Katz B. G. , Catches J. S. , Bullen T. D. , Michel R. L. ,
The Little River, an ephemeral stream that drains a watershed of approximately ss km(2) in northern Florida, disappears into a series of sinkholes along the Cody Scarp and flows directly into the carbonate Upper Floridan aquifer, the source of water supply in northern Florida. The changes in the geochemistry of ground water caused by a major recharge pulse from the sinking stream were investigated using chemical and isotopic tracers and mass-balance modeling techniques, Nine monitoring wells were installed open to the uppermost part of the aquifer in areas near the sinks where numerous subterranean karst solution features were identified using ground penetrating radar. During high-flow conditions in the Little River, the chemistry of water in some of the monitoring wells changed, reflecting the mixing of river water with ground water. Rapid recharge of river water into some parts of the aquifer during high-flow conditions was indicated by enriched values of delta O-18 and delta deuterium (-1.67 to -3.17 per mil and -9.2 to -15.6 per mil, respectively), elevated concentrations of tannic acid, higher (more radiogenic) Sr-87/Sr-86 ratios, and lower concentrations of Rn-222, silica, and alkalinity compared to low-how conditions. The proportion of river water that mixed with ground water ranged from 0.10 to 0.67 based on binary mixing models using the tracers O-18, deuterium, tannic acid, silica, Rn-222, and Sr-87/Sr-86. On the basis of mass-balance modeling during steady-state how conditions, the dominant processes controlling carbon cycling in ground water are the dissolution of calcite and dolomite in aquifer material, and aerobic degradation of organic matter. (C) 1998 Elsevier Science B.V. All rights reserved

Oxidation of organic matter in a karstic hydrologic unit supplied through stream sinks (Loiret, France), 1998, Alberic P, Lepiller M,
The aim of this paper is to appraise the ability of the oxidation of riverine organic matter in the control of limestone dissolution, in a karst network. Biogeochemical processes during infiltration of river water into an alluvial aquifer have already been described for an average flow velocity of 4-5 m d(-1) (Jacobs, L. A., von Gunten, H. R., Keil, R, and Kuslys, M. (1988) Geochemical changes along a river-groundwater infiltration flow path: Glattfelden, Switzerland. Geochim. Cosmochim. Acta 52, 2693-2706; Von Gunten, H. R., Karametaxas, G., Krahenbuhl, U., Kuslys, M., Giovanoli R., Hoehn E. and Keil R. (1991) Seasonal biogeochemical cycles in riverborne groundwater. Geochim. Cosmochim. Acta 55, 3597-3609; Bourg, A. C. M. and Bertin, C. (1993) Quantitative appraisal of biogeochemical chemical processes during the infiltration of river water into an alluvial aquifer. Environ. Sci. Technol. 27, 661-666). Karstic drainage networks, such as in the River Loire-Val d'Orleans hydrologic system (Fig. 1), make possible flow velocities up to 200 m h(-1 a) and provide convenient access to different water samples several tens of km apart, at both extremities of the hydrologic unit (Chery, J.-L. (1983) Etude hydrochimique d'un aquifere karstique alimente par perte de cours d'eau (la Loire): Le systeme des calcaires de Beauce sous le val d'Orleans. These, Universite d'Orleans; Livrozet, E. (1984) Influence des apports de la Loire sur la qualite bacteriologique et chimique de l'aquifere karstique du val d'Orleans. These, Universite d'Orleans). Recharge of the karstic aquifer occurs principally from influent waters from stream sinks, either through coarse alluvial deposits or directly from outcrops of the regional limestone bedrock (Calcaires de Beauce). Recharge by seepage waters From the local catchment basin is small (Zunino, C., Bonnet, M. and Lelong, F. (1980) Le Val d'Orleans: un exemple d'aquifere a alimentation laterale. C. R. somm. Soc. Geol. Fr. 5, 195-199; Gonzalez R. (1992) Etude de l'organisation et evaluation des echanges entre la Loire moyenne et l'aquifere des calcaires de Beauce. These, Universite d'Orleans) and negligible in summer. This karstic hydrologic: system is the largest in France in terms of flow (tens to hundreds of m(3)/s) and provides the main water resource of the city of Orleans. Chemical compositions of influent waters (River Loire) and effluent waters (spring of the river Loiret) were compared, in particular during floods in summer 1992 and 1993 (Figs 2-4). Variation of chloride in the River Loire during the stream rise can be used as an environmental tracer of the underground flow (Fig. 2). Short transit times of about 3 days are detectable (Fig, 2) which are consistent with earlier estimations obtained with chemical tracers (Ref. in Chery, J.-L. (1983) These, Universite d'Orleans). Depending on the hydrological regime of the river, organic carbon discharge ranges between 3-7 and 2-13 mg/l for dissolved and particulate matter respectively (Fig. 3). Eutrophic characteristics and high algal biomasses are found in the River Loire during low water (Lair, N. and Sargos, D. (1993) A 10 year study at four sites of the middle course of the River Loire. I - Patterns of change in hydrological, physical and chemical variables in relation to algal biomass. Hudroecol. Appl. 5, 1-27) together with more organic carbon rich suspended particulate matter than during floods (30-40 C-org % dry weight versus 5-10%). Amounts of total organic carbon and dissolved oxygen (Fig. 3) dramatically decrease during the underground transport, whereas conversely, dissolved calcium, alkalinity and inorganic carbon increase (Fig. 4). Anoxia of outflows map start in April. Dissolution of calcium carbonates along the influent path outweighs closed system calcite equilibrium of inflow river waters (Table 3). The impact of organic matter oxidation on calcite dissolution may be traced by variations of alkalinity and total carbonates in water. Following, Jacobs, L. A., von Gunten, H. R., Keil, R. and Kuslys, M. (1988) Geochemical changes along a river-groundwater infiltration flow path: Glattfelden, Switzerland. Geochim. Cosmochim. Acta 52, 2693-2706), results are shown graphically (Fig. 5). Extent of reactions is controlled by the consumption of dissolved O-2 and nitrate for organic matter oxidation and by the release of Ca2 for calcite dissolution (Table 2). The karstic network is considered to behave like a biological reactor not exchanging with the atmosphere, with steady inhabitant microbial communities (Mariotti A., Landreau A, and Simon B. (1988) N-15 isotope biogeochemisrry and natural denitrification process in groundwater: Application to the chalk aquifer of northern France. Geochim. Cosmochim. Acta 52, 1869-1878; Gounot, A.-M. (1991) Ecologie microbienne des eaux ei des sediments souterrains. Hydrogeologie, 239-248). Thus, energy requirements only are considered, not carbon assimilation. Moreover, there is no necessity to invoke any delay for nitrification enhancement, as observed elsewhere, after waste water discharge into the river (Chesterikoff, A., Garban, B., Billen, G. and Poulin, M. (1992) Inorganic nitrogen dynamics in the River Seine downstream from Paris (France). Biogeochem. 17, 147-164). Main microbial processes are assumed to be aerobic respiration, nitrification and denitrification. Reactions with iron and manganese, real but not quantitatively important, were neglected. Sulphate reduction and methane formation, certainly not active, were not considered. Denitrification, which is suggested by low nitrate and ammonium concentrations and anoxia in the outflow, is known to be rapid enough to be achieved in a short time (Dupain, S. (1992) Denitrification biologique heterotrophe appliquee au traitement des eaux d'alimentation: Conditions de fonclionnement et mise au point d'un procede. These, Universite Claude Bernard, Lyon). Reaction are somewhat arbitrary but conform to general acceptance (Morel, M. M. and Hering, J. G. (1993) Principles and Applications of Aquatic Chemistry. Wiley, New York). Anaerobic ammonium oxidation (Mulder A., van de Graaf, A. A., Robertson, L: A. and Kuenen, J. G. (1995) Anaerobic ammonium oxidation discovered in a denitrifying fluidized bed reactor. FEMS Microbiol. Ecol. 16, 177-184). although possible, was not considered. In fact, C/N ratio of the reactive organic matter has only mild repercussions on the results; i.e. in the same range as the analytical errors for alkalinity and total carbonates. The objective was simply to roughly confront characteristics of outflowing waters and the calculation. Respective roles of aerobes and denitrifiers, for instance, are not certain. Several periods during low water or floods were selected with various ranges for calcium dissolution or nitrate and oxygen concentrations. The result is that in most cases simulation and data are in reasonable accordance (Fig. 5). Amounts of organic matter in River Loire are generally sufficient to sustain the process (Table 3. Particulate organic matter is probably the most reactive. The balance of oxidation of organic matter indicates that about 65 mu g C-org/l.h are oxidized during the transport without much variation with the river regime or organic discharge. It is concluded that limestone dissolution is directly dependent on organic matter oxidation, but variation occurs (7-29 mg CuCO3/l) with the level of bases that can be neutralized in the River Loire water. (C) 1998 Elsevier Science Ltd. All rights reserved

Searching for a 3-way model of spatial and seasonal variations in the chemical composition of karstic freshwaters, 1999, Barbieri P, Adami G, Reisenhofer E,
A procedure is described for the search of a three,way;principal components model, characterizing a data set concerning the spatial and temporal distribution of the physico-chemical parameters which govern the composition of waters collected from springs, ponds and;rivers of the Karst of Trieste. Ten physico-chemical parameters were determined-for eleven sampling sites and eleven sampling times. A:graphic method was applied in order to find the number of components in each of the three ways of the model, explaining a relatively high quantity of variation of the. data, with a limited number of components, i.e. with descriptive parsimony, and generating interpretable factors. The examination of 125 possible Tucker3 models, having from 1 to 5 components in each of the ways, allowed us to identify the model having two components in each of the three ways as the one satisfying the desired criteria. The chance of reducing to a simpler PARAFAC model has been successfully explored,and two trilinear components were then computed. The first one is mainly related to a spatial factor conditioning the considered waters, while the second is related to a seasonal factor

Chemical composition of landfill leachate in a karst area with a Mediterranean climate (Marbella, southern Spain), 1999, Vadillo I. , Carrasco F. , Andreo B. , De Torres A. , Bosch C. ,

Hydrochemical evidence for mixing of river water and groundwater during high-flow conditions, lower Suwannee River basin, Florida, USA, 1999, Crandall Ca, Katz Bg, Hirten Jj,
Karstic aquifers are highly susceptible to rapid infiltration of river water, particularly during periods of high flow. Following a period of sustained rainfall in the Suwannee River basin, Florida, USA, the stage of the Suwannee River rose from 3.0 to 5.88 m above mean sea level in April 1996 and discharge peaked at 360 m(3)/s. During these high-now conditions, water from the Suwannee River migrated directly into the karstic Upper Floridan aquifer, the main source of water supply for the area. Changes in the chemical composition of groundwater were quantified using naturally occurring geochemical tracers and mass-balance modeling techniques. Mixing of river water with groundwater was indicated by a decrease in the concentrations of calcium, silica, and Rn-222; and by an increase in dissolved organic carbon (DOC), tannic acid, and chloride, compared to low-flow conditions in water from a nearby monitoring well, Wingate Sink, and Little River Springs. The proportion (fraction) of river water in groundwater ranged from 0.13 to 0.65 at Wingate Sink and from 0.5 to 0.99 at well W-17258, based on binary mixing models using various tracers. The effectiveness of a natural tracer in quantifying mixing of river water and groundwater was related to differences in tracer concentration of the two end members and how conservatively the tracer reacted in the mixed water. Solutes with similar concentrations in the two end-member waters (Na, Mg, K, Cl, SO4, SiO2) were not as effective tracers for quantifying mixing of river water and groundwater as those with larger differences in end-member concentrations (Ca, tannic acid, DOC, Rn-222, HCO3)

Influence of contaminated Vistula River water on the groundwater entering the Zakrzowek limestone quarry, Cracow region, Poland, 2000, Motyka J. , Postawa A. ,
Chemical composition of water inflows in the Zakrzowek quarry, developed in fractured and karstified Upper Jurassic limestones, is controlled by infiltration of polluted water from the Vistula River and by infiltrating meteoric water. The river water TDS value is 2.5 g/dm(3). The quarry waters have 0.6-2.0 g/dm(3) TDS. Highly mineralised waters belong to Cl-Na type. With decreasing TDS the percentage of sulphates, calcium, magnesium and hydrocarbonates increases. This seems to result from various processes including dilution of polluted river water, leaching of aquifer rocks, and ion exchange. The transfer time of river water to the quarry is about 100-120 days. Concentration of contaminants contained in the river water declines during the migration through limestones to the quarry

Element geochemistry of weathering profile of dolomitite and its implications for the average chemical composition of the upper-continental crust - Case studies from the Xinpu profile, northern Guizho, 2000, Ji H. B. , Ouyang Z. , Wang S. J. , Zhou D. Q. ,
Geochemical behavior of chemical elements is studied in a dolomitite weathering profile in upland of karst terrain in northern Guizhou. Two stages can be recognized during the process of in situ weathering of dolomitite: the stage of sedentary accumulation of leaching residue of dolomitite and the stage of chemical weathering evolution of sedentary soil. Ni, Cr, Mo, W and Ti are the least mobile elements with reference to Al. The geochemical behavior of REE is similar to that observed in weathering of other types of rocks. Fractionation of REE is noticed during weathering, and the two layers of REE enrichments are thought to result from downward movement of the weathering front in response to changes in the environment. It is considered that the chemistry of the upper part of the profile, which was more intensively weathered, is representative of the mobile components of the upper curst at the time the dolomitite was formed, while the less weathered lower profile is chemically representative of the immobile constitution. Like glacial till and loess, the 'insoluble' materials in carbonate rocks originating from chemical sedimentation may also provide valuable information about the average chemical composition of the upper continental crust

Role of mixing corrosion in calcite-aggressive H2O-CO2-CaCO3 solutions in the early evolution of karst aquifers in limestone, 2000, Gabrovsek F, Dreybrodt W,
Two cave-forming mechanisms in limestone are discussed currently. First, when two H2O-CO2-CaCO3 solutions, saturated with respect to calcite but with different chemical compositions mix, renewed aggressiveness to limestone dissolution occurs. This process called mixing corrosion [Bogli, 1964, 1980], in combination with linear dissolution kinetics, has been suggested as cave forming. Second, it has been shown that solely the action of nonlinear dissolution kinetics can generate extended karst conduits. This paper combines both mechanisms. By digital modeling of the evolution of the aperture widths of a confluence of two fractures into a third one it is shown that the first mechanism does not create large cave conduits. The combination of mixing corrosion and nonlinear kinetics, however, considerably intensifies karstification, compared to that of nonlinear kinetics solely. The times to terminate early evolution of karst are significantly reduced when the CO2 concentrations of the inflowing solutions differ by no more than 30%. We discuss the underlying mechanisms by inspection of the time dependence of the evolution of aperture widths, flow rates through them, and of the renewed undersaturation of the mixed solution at the confluence of two fractures. Finally, the evolution of a karst aquifer on a two-dimensional percolation network is modeled when mixing corrosion is present, and compared to that on an identical net with identical nonlinear dissolution kinetics, but mixing corrosion excluded. Large differences in the morphology of the net of cave conduits are found and also a reduction of the time of their evolution. From these findings we conclude that climatic changes, which influence the p(CO2) in the soil, can divert the evolving cave patterns

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