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1.
Formation of extensive phreatic caves in eogenetic karst aquifers is widely believed to require mixing of fresh and saltwater. Extensive phreatic caves also occur, however, in eogenetic karst aquifers where fresh and saltwater do not mix, for example in the upper Floridan aquifer. These caves are thought to have formed in their modern settings by dissolution from sinking streams or by convergence of groundwater flow paths on springs. Alternatively, these caves have been hypothesized to have formed at lower water tables during sea level low‐stands. These hypotheses have not previously been tested against one another. Analyzing morphological data and water chemistry from caves in the Suwannee River Basin in north‐central Florida and water chemistry from wells in the central Florida carbonate platform indicates that phreatic caves within the Suwannee River Basin most likely formed at lower water tables during lower sea levels. Consideration of the hydrological and geochemical constraints posed by the upper Floridan aquifer leads to the conclusion that cave formation was most likely driven by dissolution of vadose CO2 gas into the groundwater. Sea level rise and a wetter climate during the mid‐Holocene lifted the water table above the elevation of the caves and placed the caves tens of meters below the modern water table. When rising water tables reached the land surface, surface streams formed. Incision of surface streams breached the pre‐existing caves to form modern springs, which provide access to the phreatic caves. Phreatic caves in the Suwannee River Basin are thus relict and have no causal relationship with modern surficial drainage systems. Neither mixing dissolution nor sinking streams are necessary to form laterally extensive phreatic caves in eogenetic karst aquifers. Dissolution at water tables, potentially driven by vadose CO2 gas, offers an underappreciated mechanism to form cavernous porosity in eogenetic carbonate rocks. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

2.
Mixing dissolution, a process whereby mixtures of two waters with different chemical compositions drive undersaturation with respect to carbonate minerals, is commonly considered to form cavernous macroporosity (e.g. flank margin caves and banana holes) in eogenetic karst aquifers. On small islands, macroporosity commonly originates when focused dissolution forms globular chambers lacking entrances to the surface, suggesting that dissolution processes are decoupled from surface hydrology. Mixing dissolution has been thought to be the primary dissolution process because meteoric water would equilibrate rapidly with calcium carbonate as it infiltrates through matrix porosity and because pCO2 was assumed to be homogeneously distributed within the phreatic zone. Here, we report data from two abandoned well fields in an eogenetic karst aquifer on San Salvador Island, Bahamas, that demonstrate pCO2 in the phreatic zone is distributed heterogeneously. The pCO2 varied from less than log ?2.0 to more than log ?1.0 atm over distances of less than 30 m, generating dissolution in the subsurface where water flows from regions of low to high pCO2 and cementation where water flows from regions of high to low pCO2. Using simple geochemical models, we show dissolution caused by heterogeneously distributed pCO2 can dissolve 2.5 to 10 times more calcite than the maximum amount possible by mixing of freshwater and seawater. Dissolution resulting from spatial variability in pCO2 forms isolated, globular chambers lacking initial entrances to the surface, a morphology that is characteristic of flank margin caves and banana holes, both of which have entrances that form by erosion or collapse after cave formation. Our results indicate that heterogeneous pCO2, rather than mixing dissolution, may be the dominant mechanism for observed spatial distribution of dissolution, cementation and macroporosity generation in eogenetic karst aquifers and for landscape development in these settings. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

3.
Caves deliver freshwater from coastal carbonate landscapes to estuaries but how these caves form and grow remains poorly understood. Models suggest fresh and salt water mixing drives dissolution in eogenetic limestone, but have rarely been validated through sampling of mixing waters. Here we assess controls on carbonate mineral saturation states using new and legacy geochemical data that were collected in vertical profiles through three cenotes and one borehole in the Yucatan Peninsula. Results suggest saturation states are primarily controlled by carbon fluxes rather than mixing. Undersaturation predicted by mixing models that rely on idealized end members is diminished or eliminated when end members are collected from above and below actual mixing zones. Undersaturation due to mixing is limited by CO2 degassing from fresh water in karst windows, which results in calcite supersaturation. With respect to saline groundwater, controls on capacity for mixing dissolution were more varied. Oxidation of organic carbon increased pCO2 of saline groundwater in caves (pCO2 = 10–2.06 to 10–0.96 atm) relative to matrix porosity (10–2.39 atm) and local seawater (10–3.12 atm). The impact of increased pCO2 on saturation state, however, depended on the geochemical composition of the saline water and the magnitude of organic carbon oxidation. Carbonate undersaturation due to mixing was limited where gypsum dissolution (Cenote Angelita) or sulfate reduction (Cenote Calica) increased concentrations of common ions (Ca2+ or HCO3?, respectively). Maximum undersaturation was found to occur in mixtures including saline water that had ion concentrations and ratios similar to seawater, but with moderately elevated pCO2 (Cenote Eden). Undersaturation, however, was dominated by the initial undersaturation of the saline end member, mixing was irrelevant. Our results add to a growing body of literature that suggests oxidation of organic carbon, and not mixing dissolution, is the dominant control on cave formation and enlargement in coastal eogenetic karst aquifers. Copyright © 2016 John Wiley & Sons, Ltd.  相似文献   

4.
Growing evidence suggests microbial respiration of dissolved organic carbon (DOC) may be a principal driver of subsurface dissolution and cave formation in eogenetic carbonate rock. Analyses of samples of vadose zone gasses, and geochemical and hydrological data collected from shallow, uncased wells on San Salvador Island, Bahamas, suggest tidally varying water tables may help fuel microbial respiration and dissolution through oxygenation. Respiration of soil organic carbon transported to water tables generates dysaerobic to anaerobic groundwater, limiting aerobic microbial processes. Positive correlations of carbon dioxide (CO2), radon-222 (222Rn) and water table elevation indicate, however, that tidal pumping of water tables pulls atmospheric air that is rich in oxygen, and low in CO2 and 222Rn, into contact with the tidal capillary fringe during falling tides. Ratios of CO2 and O2 in vadose gas relative to the atmosphere indicate this atmospheric oxygen fuels respiration within newly-exposed, wetted bedrock. Deficits of expected CO2 relative to O2 concentrations indicate some respired CO2 is likely removed by carbonate mineral dissolution. Tidal pumping also appears capable of transferring oxygen to the freshwater lens, where it could also contribute to respiration and dissolution; dissolved oxygen concentrations at the water table are at least 5% saturated and decline to anaerobic conditions 1–2 m below. Our results demonstrate how tidal pumping of air to vadose zones can drive mineral dissolution reactions that are focused near water tables and may contribute to the formation of laterally continuous vuggy horizons and potentially caves. © 2020 John Wiley & Sons, Ltd.  相似文献   

5.
Florea LJ  Vacher HL 《Ground water》2007,45(4):439-446
Eogenetic karst lies geographically and temporally close to the depositional environment of limestone in warm marine water at low latitude, in areas marked by midafternoon thunderstorms during a summer rainy season. Spring hydrographs from such an environment in north-central Florida are characterized by smooth, months-long, seasonal maxima. The passage of Hurricanes Frances and Jeanne in September 2004 over three field locations shows how the eogenetic karst of the Upper Floridan Aquifer responds to unequivocal recharge events. Hydrographs at wells in the High Springs area, Rainbow Springs, and at Morris, Briar, and Bat Caves all responded promptly with a similar drawn-out rise to a maximum that extended long into the winter dry season. The timing indicates that the typical hydrograph of eogenetic karst is not the short-term fluctuations of springs in epigenic, telogenetic karst, or the smoothed response to all the summer thunderstorms, but rather the protracted response of the system to rainfall that exceeds a threshold. The similarity of cave and noncave hydrographs indicates distributed autogenic recharge and a free communication between secondary porosity and permeable matrix-both of which differ from the hydrology of epigenic, telogenetic karst. At Briar Cave, drip rates lagged behind the water table rise, suggesting that recharge was delivered by fractures, which control the cave's morphology. At High Springs, hydrographs at the Santa Fe River and a submerged conduit apparently connected to it show sharp maxima after the storms, unlike the other cave hydrographs. Our interpretation is that the caves, in general, are discontinuous.  相似文献   

6.
In the past few years the systematic study of caves intercepted by mine workings in southwest Sardinia has permitted us to observe morphologies due to rare speleogenetic and minerogenetic processes related to ancient hydrothermal activity. These relic morphologies are slowly being overprinted by recent speleogenetic processes that tend to obscure the hypogene origin of these caves. A combined geomorphological and mineralogical investigation has permitted a fairly detailed reconstruction of the various phases of evolution of these caves. Cave formation had already started in Cambrian times, but culminated in the Carboniferous, when most of the large voids still accessible today were formed. A key role in carbonate dissolution was played by sulphuric acid formed by the oxidation of the polymetallic ores present in the rocks since the Cambrian. During the Quaternary a variety of minerals formed inside the caves: calcite and aragonite, that yielded sequences of palaeo‐environmental interest, and also barite, phosgenite, hydrozincite, hemimorphite and many others. These minerals are in part due to a phreatic thermal hypogenic cave forming phase, and in part to later epigene overprinting in an oxidizing environment rich in polymetallic ores. Massive gypsum deposits, elsewhere typical of this kind of caves, are entirely absent due to dissolution during both the phreatic cave formation and the later epigenic stage. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   

7.
Under field conditions modern digital conductivity meters give standardized, rapid and reproducible measurements. Here we investigate the accuracy of their estimates of the composition of karst waters, as total hardness (TH, as mg/L CaCO3) for limestone and dolomite. These are the fundamental measures of process in carbonate karst geomorphology. PHREEQC theoretical curves for the dissolution of pure calcite/aragonite and dolomite in water at 25 °C are compared with water analyses from karst studies worldwide. Other principal ions encountered are sulphates, nitrates and chlorides (the ‘SNC’ group). From carbonate karsts, 2309 spring, well and stream samples were divided into uncontaminated (SNC < 10%), moderately contaminated (10 < SNC < 20%), and contaminated (SNC > 20%) classes. Where specific conductivity (SpC) is less than 600 µS/cm, a clear statistical distinction can be drawn between waters having little contamination and substantially contaminated waters with SNC > 20%. As sometimes claimed in manufacturers' literature, in ‘clean’ limestone waters TH is close to 1/2SpC, with a standard error of 2–3 mg/L. The slope of the best‐fit line for 1949 samples covering all SNC classes where SpC < 600 µS/cm is 1·86, very close to the 1·88 obtained for clean limestone waters; however, the value of the intercept is ten times higher. The regression line for clean limestone waters where SpC > 600 µS/cm helps to distinguish polluted waters from clean waters with possible endogenic sources of CO2. In the range 250 < SpC < 600 µS/cm, dolomite waters can be readily distinguished from limestone waters. Copyright © 2005 John Wiley & Sons, Ltd.  相似文献   

8.
Extreme heterogeneity of karst systems makes them very challenging to study. Various processes within the system affect its global response, usually measured at karst springs. Research conducted in caves provides a unique opportunity for in situ analysis of separate processes in karst underground. The aim of the present study was to research the water and air dynamics within a deep karst system. Air and water basic physical parameters across the Lukina jama–Trojama cave system (?1,431 m) were continuously monitored during a 1‐year period. Recorded hydrograph of the siphon lake at the bottom of the cave was used to interpret the characteristics of an unexplored phreatic/epiphreatic conduit network. Water origin in the siphon was determined based on temperature and electrical conductivity. Air temperature and humidity monitoring revealed a strong inflow of air of sub‐zero temperature into the upper portion of the cave during winter. Cave passage morphology was interpreted as the main determinant of air dynamics, which caused ice to accumulate extensively in the upper portions of the cave and caused the temperature on the top of the homothermic zone to be significantly below the mean outside temperature. Air dynamics also lowered the temperature of water flowing through the cave vadose zone and feeding the phreatic zone of the massif. The pronounced temperature difference between the phreatic zone and the top of the homothermic zone probably contributed to the thermal gradient observed in the cave, which is steeper than in ice‐free caves in the area. Our results enabled the development of a conceptual model that describes coupling between air and water dynamics in the cave system and its surroundings.  相似文献   

9.
Cave air PCO2 at two Irish sites varied dramatically on daily to seasonal timescales, potentially affecting the timing of calcite deposition and consequently climate proxy records derived from stalagmites collected at the same sites. Temperature-dependent biochemical processes in the soil control CO2 production, resulting in high summer PCO2 values and low winter values at both sites. Large Large-amplitude, high-frequency variations superimposed on this seasonal cycle reflect cave air circulation. Here we model stalagmite growth rates, which are controlled partly by CO2 degassing rates from drip water, by considering both the seasonal and high-frequency cave air PCO2 variations. Modeled hourly growth rates for stalagmite CC-Bil from Crag Cave in SW Ireland reach maxima in late December (0.063 μm h− 1) and minima in late June/early July (0.033 μm h− 1). For well-mixed ‘diffuse flow’ cave drips such as those that feed CC-Bil, high summer cave air PCO2 depresses summer calcite deposition, while low winter PCO2 promotes degassing and enhances deposition rates. In stalagmites fed by well-mixed drips lacking seasonal variations in δ18O, integrated annual stalagmite calcite δ18O is unaffected; however, seasonality in cave air PCO2 may influence non-conservative geochemical climate proxies (e.g., δ13C, Sr/Ca). Stalagmites fed by ‘seasonal’ drips whose hydrochemical properties vary in response to seasonality may have higher growth rates in summer because soil air PCO2 may increase relative to cave air PCO2 due to higher soil temperatures. This in turn may bias stalagmite calcite δ18O records towards isotopically heavier summer drip water δ18O values, resulting in elevated calcite δ18O values compared to the ‘equilibrium’ values predicted by calcite–water isotope fractionation equations. Interpretations of stalagmite-based paleoclimate proxies should therefore consider the consequences of cave air PCO2 variability and the resulting intra-annual variability in calcite deposition rates.  相似文献   

10.
The Bahama Islands contain many abandoned dissolution caves at elevations between two and seven metres above current sea level. The development of dissolution caves in tropical carbonate islands is dependent on the position and nature of the freshwater lens. Lens position is controlled by sea level, which in stable carbonate platforms like the Bahamas is a function of glacioeustatic sea level still stands. Caves in the Bahamas that are currently subaerial must have developed during past higher sea levels. During the Late Quaternary, sea levels higher than present have been relatively short-lived, and that limits the amount of time that a freshwater lens could be situated at the elevation required for the cave formation. The Bahama Islands are low-lying landforms where only aeolian ridges extend to elevations higher than six metres above current sea level. Past high sea level events greatly reduced the exposed land area of the Bahama Islands, thus also limiting both the catchment for and size of freshwater lenses. Caves must be younger than the rock in which they are developed; most subaerial Bahamian caves are found in limestones that are less than 150000 years old. Development of large dissolution caves under these limitations of time and lens size requires a powerful dissolutional mechanism. The mixing of discharging freshwater with tide-pulsed incoming marine water under the flanks of emergent dune ridges may have produced the conditions necessary. Bahamian caves formed by this process are phreatic chambers with complex interconnections and blind tubes. Their presence demonstrates that significant dissolution can occur rapidly as a result of the mixing of fresh and marine waters beneath small carbonate islands.  相似文献   

11.
In the present paper, we describe the genetic mechanism that causes the precipitation of raft cones in caves. These speleothems usually form in a hydrothermal and epiphreatic environment where dripwater, dripping repeatedly over the same spot, sinks calcite rafts that were floating on the water surface of a cave pool. In particular, the paper describes a new variety of raft cones that were recently discovered in the Paradise Chamber of the Sima de la Higuera Cave (Murcia, south‐eastern Spain) based on their morphological and morphometric characteristics. These speleothems, dubbed ‘double‐tower cones’, have a notch in the middle and look like two cones, one superimposed over the other. The genetic mechanism that gave rise to the double‐tower cones must include an intermediate stage of rapid calcite raft precipitation, caused by a drop in the water table and by changes in cave ventilation leading to greater carbon dioxide (CO2) degassing and evaporation over the surface of the thermal lake where these speleothems formed. Calcite rafts were deposited in Paradise Chamber, completely covering many of the cones. Later, conditions for slower calcite raft precipitation were restored and some of the cones continued to grow at the same points. When the water table finally fell below the level of Paradise Chamber, the tower cones became exposed, as the incongruent deposits of calcite rafts were dissolved and mobilized to lower cave levels. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   

12.
Phreatic overgrowths on speleothems (POS) are carbonate formations deposited at the water table of caves in unique karstic coastal settings having morphologies that can be directly related to sea level at the time of formation. The U‐Th ages of calcite and aragonite overgrowths collected from the modern water table in coastal caves on Mallorca (Cova de Cala Varques A and Cova des Pas de Vallgornera) were determined using high‐precision MC‐ICPMS techniques. U‐Th ages indicate that phreatic carbonate deposition occurred between ca 2·8 and at least 0·6 ka BP and are in accord with an archeologically estimated age of 3·7–3·0 ka BP for a drowned prehistoric construction at a depth of 1 m below current sea level in a cave from the same area. Speleothem δ13C and δ18O and chemical composition of cave pools provide supportive evidence that POS reflect mixing between seawater and brackish water table. Copyright © 2010 John Wiley & Sons, Ltd.  相似文献   

13.
We used the 3D continuum-scale reactive transport models to simulate eight core flood experiments for two different carbonate rocks. In these experiments the core samples were reacted with brines equilibrated with pCO2 = 3, 2, 1, 0.5 MPa (Smith et al., 2013 [27]). The carbonate rocks were from specific Marly dolostone and Vuggy limestone flow units at the IEAGHG Weyburn-Midale CO2 Monitoring and Storage Project in south-eastern Saskatchewan, Canada. Initial model porosity, permeability, mineral, and surface area distributions were constructed from micro tomography and microscopy characterization data. We constrained model reaction kinetics and porosity–permeability equations with the experimental data. The experimental data included time-dependent solution chemistry and differential pressure measured across the core, and the initial and final pore space and mineral distribution. Calibration of the model with the experimental data allowed investigation of effects of carbonate reactivity, flow velocity, effective permeability, and time on the development and consequences of stable and unstable dissolution fronts.The continuum scale model captured the evolution of distinct dissolution fronts that developed as a consequence of carbonate mineral dissolution and pore scale transport properties. The results show that initial heterogeneity and porosity contrast control the development of the dissolution fronts in these highly reactive systems. This finding is consistent with linear stability analysis and the known positive feedback between mineral dissolution and fluid flow in carbonate formations. Differences in the carbonate kinetic drivers resulting from the range of pCO2 used in the experiments and the different proportions of more reactive calcite and less reactive dolomite contributed to the development of new pore space, but not to the type of dissolution fronts observed for the two different rock types. The development of the dissolution front was much more dependent on the physical heterogeneity of the carbonate rock. The observed stable dissolution fronts with small but visible dissolution fingers were a consequence of the clustering of a small percentage of larger pores in an otherwise homogeneous Marly dolostone. The observed wormholes in the heterogeneous Vuggy limestone initiated and developed in areas of greater porosity and permeability contrast, following pre-existing preferential flow paths.Model calibration of core flood experiments is one way to specifically constrain parameter input used for specific sites for larger scale simulations. Calibration of the governing rate equations and constants for Vuggy limestones showed that dissolution rate constants reasonably agree with published values. However the calcite dissolution rate constants fitted to the Marly dolostone experiments are much lower than those suggested by literature. The differences in fitted calcite rate constants between the two rock types reflect uncertainty associated with measured reactive surface area and appropriately scaling heterogeneous distribution of less abundant reactive minerals. Calibration of the power-law based porosity–permeability equations was sensitive to the overall heterogeneity of the cores. Stable dissolution fronts of the more homogeneous Marly dolostone could be fit with the exponent n = 3 consistent with the traditional Kozeny–Carman equation developed for porous sandstones. More impermeable and heterogeneous cores required larger n values (n = 6–8).  相似文献   

14.
A simulation was undertaken within a climatic chamber to investigate limestone dissolution under varied carbonic acid (H2CO3) strengths as a possible analogue for future increases in atmospheric CO2 arising from global warming. Twenty‐eight samples cut from a block of Bath (Box Hill) limestone from Somerville College, Oxford, which had been removed during restoration after 150 years in an urban environment, were weighed and placed in closed bottles of thin plastic containing varying concentrations of H2CO3. Half of the stone samples were derived from exposed surfaces of the stone block (weathered) while the others were obtained from the centre of the block on unexposed surfaces (unweathered). The purpose of this was to compare dissolution of previously weathered versus unweathered surfaces in strong (pH 4·73) versus weak (pH 6·43) solutions of H2CO3. A temperature of c. 19 °C was maintained within the chamber representing a plausible future temperature in Oxford for the year 2200 given current warming scenarios. The simulation lasted 25 days with a few stone samples being removed midway. Stone samples show reduced weight in all cases but one. There was greater dissolution of stone samples in a strong H2CO3 solution as conveyed by higher concentrations of total hardness and Ca2+ in the water samples as well as enhanced microscopic dissolution features identified using SEM. The simulation confirms that enhanced atmospheric CO2 under global warming, given adequate moisture, will accelerate dissolution rates particularly of newly replaced limestone building stones. However, previously weathered surfaces, such as those on historical stone exposed for a century or more, appear to be less susceptible to the effects of such increased rainfall acidity. Conservation techniques which remove weathered surfaces, such as stone cleaning, may accelerate future decay of historical limestone structures by increasing their susceptibility to dissolution. Copyright © 2006 John Wiley & Sons, Ltd.  相似文献   

15.
This study is undertaken to understand how calcite precipitation and dissolution contributes to depth-related changes in porosity and permeability of gas-bearing sandstone reservoirs in the Kela 2 gas field of the Tarim Basin, Northwestern China. Sandstone samples and pore water samples are col-lected from well KL201 in the Tarim Basin. Vertical profiles of porosity, permeability, pore water chem-istry, and the relative volume abundance of calcite/dolomite are constructed from 3600 to 4000 m below the ground surface within major oil and gas reservoir rocks. Porosity and permeability values are in-versely correlated with the calcite abundance, indicating that calcite dissolution and precipitation may be controlling porosity and permeability of the reservoir rocks. Pore water chemistry exhibits a sys-tematic variation from the Na2SO4 type at the shallow depth (3600-3630 m), to the NaHCO3 type at the intermediate depth (3630―3695 m),and to the CaCl2 type at the greater depth (3728―3938 m). The geochemical factors that control the calcite solubility include pH, temperature, pressure, Ca2 concen-tration, the total inorganic carbon concentration (ΣCO2), and the type of pore water. Thermodynamic phase equilibrium and mass conservation laws are applied to calculate the calcite saturation state as a function of a few key parameters. The model calculation illustrates that the calcite solubility is strongly dependent on the chemical composition of pore water, mainly the concentration difference between the total dissolved inorganic carbon and dissolved calcium concentration (i.e., [ΣCO2] -[Ca2 ]). In the Na2SO4 water at the shallow depth, this index is close to 0, pore water is near the calcite solubility. Calcite does not dissolve or precipitate in significant quantities. In the NaHCO3 water at the intermedi-ate depth, this index is greater than 0, and pore water is supersaturated with respect to calcite. Massive calcite precipitation was observed at this depth interval and this intensive cementation is responsible for decreased porosity and permeability. In the CaCl2 water at the greater depth, pore water is un-der-saturated with respect to calcite, resulting in dissolution of calcite cements, as consistent with microscopic dissolution features of the samples from this depth interval. Calcite dissolution results in formation of high secondary porosity and permeability, and is responsible for the superior quality of the reservoir rocks at this depth interval. These results illustrate the importance of pore water chemis-try in controlling carbonate precipitation/dissolution, which in turn controls porosity and permeability of oil and gas reservoir rocks in major sedimentary basins.  相似文献   

16.
The precipitation of freshwater carbonates (tufa) along karstic rivers is enhanced by degassing of carbon dioxide (CO2) downstream of karstic springs. However, in most karstic springs CO2 degassing is not enough to force the precipitation of tufa sediments. Little is known about the role of dissolution of gypsum or dolomite in the hydrochemistry of these systems and how this affects the formation of tufa deposits. Here we present a monitoring study conducted over a year in Trabaque River (Spain). The river has typical karst hydrological dynamics with water sinking upstream and re‐emerging downstream of the canyon. Mixing of calcium–magnesium bicarbonate and calcium sulphate waters downstream of the sink enhances the dissolution of carbonates and potentially plays a positive role in the formation of tufa sediments. However, due to the common‐ion effect, dissolution of dolomite and/or gypsum causes precipitation of underground calcite cements as part of the incongruent dissolution of dolomite/dedolomitization process, which limits the precipitation of tufa sediments. Current precipitation of tufa is scant compared to previous Holocene tufa deposits, which likely precipitated from solutions with higher saturation indexes of calcite (SIcc values) than nowadays. Limited incongruent dissolution of dolomite/dedolomitization favours higher SIcc values. This circumstance occurs when waters with relatively high supersaturation of dolomite and low SO42? composition sink in the upper sector of the canyon. In such a scenario, the process of mixing waters enhances the exclusive dissolution of limestones, preventing the precipitation of calcite within the aquifer and favouring the increase of SIcc values downstream of the springs. Such conditions were recorded during periods of high water level of the aquifers and during floods. This research shows that the common‐ion effect caused by the dissolution of gypsum and/or dolomite rocks can limit [or favour] the precipitation of tufa sediments depending on the occurrence [or not] of incongruent dissolution of dolomite/dedolomitization. Copyright © 2016 John Wiley & Sons, Ltd.  相似文献   

17.
Uranium-series ages have been obtained for 87 speleothems collected from nine major cave systems in the Craven district of northern England. Large systems such as Ease Gill Caverns, the West Kingsdale caves, and Gaping Gill-Ingleborough Cave, which contain relict high-level tunnels, are found to be older than 350,000 years (the limit of the 230Th/234U dating method). There is little evidence to indicate a significant enlargement of these passages since this time. Estimates of the age of Victoria Cave from 234U/238U isotopic ratios suggest that the cave has been fully relict for more than 500,000 years. Ages of in situ speleothems immediately adjacent to local base level cave streams show that mean maximum downcutting rates in limestone channels are about 2 to 5 cm 1000 yr. These rates are significantly lower than those obtained from direct measurements on limestone bedrock in stream channels but are comparable to areal denudation rates based on solute budgets. Using the present elevation of caves with respect to adjacent valley floor levels, mean maximum valley entrenchment rates are found to range between 5 cm/ky and < 20cm/ky, which corresponds to 6 m to < 24 m of lowering per glacial/interglacial cycle. These rates suggest that upper beds of the limestone were incised to form the Yorkshire Dales between 1 and 2 million years ago. The results indicate that the erosional effects of individual glaciations are not as severe as previously proposed in the literature.  相似文献   

18.
Aggtelek National Park, Hungary, is a limestone karst upland characterized by karren, dolines and river caves. For a period of two years, climatic and carbonate dissolution variables were monitored at four depths in a 7·5 m shaft through the soil fill in the floor of a typical large (150 m diameter) doline. Results are compared to other monitoring stations in the shallow soils on side slopes. Runoff and groundwater flow are focused into the base of the doline soil fill, where moisture is maintained at 70–90 per cent field capacity and temperatures permit year-round production of soil CO2. The capacity to dissolve calcite (limestone) ranges from c. 3 g m−2 per year beneath thin soils on the driest slopes to 17–30 g m−2 per year in the top 1–2 m of doline fill and at its base 5–7 m below. © 1997 John Wiley & Sons, Ltd.  相似文献   

19.
The maze caves of the Northern Pennines are rectilinear joint-controlled networks of predominantly tall vertical rifts developed on one level towards the top of a ~20 m thick limestone bed; they were all intersected by underground mines and have no relationship to the present landscape. Passage walls commonly have large, non-directional scallops; speleothems are uncommon. The caves were previously identified as hypogene in origin, i.e. formed by groundwater ascending from depth, but reassessment of their origin using published data shows that they lack diagnostic hypogene features (rising wall channels, ceiling channels, ceiling cupolas and dome-pits), and the low permeability strata above and below the limestone bed greatly restrict vertical groundwater flow through the caves. Instead the maze caves were dissolved by the sulphuric acid released by oxidation of iron sulphides (and perhaps chalcopyrite) in the mineralized veins adjacent to all these caves; passage sizes decrease away from the veins and gypsum encrusts the walls of one cave. The maze caves were not formed by vertical groundwater flow, and dissolution was focussed in a relatively small area of limestone beneath an impermeable confining layer. The caves began to form when river incision due to the probably Late Cenozoic uplift of northern England exposed the iron sulphides to weathering and oxidation. The process that formed the maze caves is here termed supergene sulphuric acid speleogenesis, because generation of the acidity was due to near-surface supergene sulphide oxidation, and differentiated from hypogene sulphuric acid speleogenesis, where the source is at depth beneath the cave. To clarify usage of the term hypogene, it should be restricted to Palmer's geochemical definition (Speleogenesis: Evolution of Karst Aquifers, eds Klimchouk et al., National Speleological Society: Huntsville, AL, 2000; 77–90): dissolution by a deep-seated source of acidity. Caves dissolved by ascending groundwater containing carbonic acid with a near-surface origin, e.g. on the rising limb of a phreatic loop, are better identified as epigene. © 2020 John Wiley & Sons Ltd  相似文献   

20.
Carbon dioxide (CO2) concentrations in caves and parent soils in the Italian Alps have been studied along a 2100 m altitudinal range – corresponding to a mean annual temperature (MAT) range of 12°C – in order to investigate the relationship between MAT, soil pCO2 and cave air pCO2, and to test the influence of soil pCO2 on speleothem growth and fabric to ultimately gain insight into their palaeoclimatic significance in temperate climate settings. Our findings indicate that soil CO2 is linearly correlated to MAT and its mean annual concentration is described by the equation: soil CO2 (ppmv) = 1112 + 460 MAT. Soil pCO2 can also be exponentially correlated to actual evapotranspiration. The pCO2 in the aquifer is linearly correlated to MAT at the infiltration site and is more influenced by summer soil pCO2. Cave air CO2 in the innermost part of the caves exhibits a similar seasonal pattern, and commonly reaches concentrations of about 15% to 35%, with respect to the corresponding soil values, and is exponentially correlated to the MAT at the infiltration site. The combination of these parameters (soil pCO2, dripwater pCO2 and cave air pCO2) results in speleothem growth and controls their fabrics which are typical of four MAT/elevation belts broadly corresponding to the present‐day vegetation zones. In the lower montane zone [100–800 m above sea level (a.s.l.)] speleothems mostly consist of columnar fabric, in the upper montane zone (800–1600 m a.s.l.) both columnar and dendritic fabrics are common, the Subalpine zone (1600–2200 m a.s.l.) is characterized mostly by moonmilk deposits, whereas in the Alpine zone (above 2200 m a.s.l.) no speleothems are forming today. Therefore, fabric changes in fossil speleothem can potentially be used to reconstruct MAT changes in temperate climate karst areas. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

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