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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 lintel line is a line on the ground at a cave entrance perpendicularly beneath the outer edge of the rock above; may or may not coincide with the dripline [25]. see also dripline.?

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.

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Chemistry and Karst, White, William B.
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Geochemical and mineralogical fingerprints to distinguish the exploited ferruginous mineralisations of Grotta della Monaca (Calabria, Italy), Dimuccio, L.A.; Rodrigues, N.; Larocca, F.; Pratas, J.; Amado, A.M.; Batista de Carvalho, L.A.
Karst environment, Culver D.C.
Mushroom Speleothems: Stromatolites That Formed in the Absence of Phototrophs, Bontognali, Tomaso R.R.; D’Angeli Ilenia M.; Tisato, Nicola; Vasconcelos, Crisogono; Bernasconi, Stefano M.; Gonzales, Esteban R. G.; De Waele, Jo
Calculating flux to predict future cave radon concentrations, Rowberry, Matt; Marti, Xavi; Frontera, Carlos; Van De Wiel, Marco; Briestensky, Milos
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Your search for organic carbon (Keyword) returned 70 results for the whole karstbase:
Showing 1 to 15 of 70
Anomalous behaviour of specific electrical conductivity at a karst spring induced by variable catchment boundaries: the case of the Podstenjšek spring, Slovenia, , Ravbar, N. , Engelhardt, I. , Goldscheider, N.

Anomalous behaviour of specific electrical conductivity (SEC) was observed at a karst spring in Slovenia during 26 high-flow events in an 18-month monitoring period. A conceptual model explaining this anomalous SEC variability is presented and reproduced by numerical modelling, and the practical relevance for source protection zoning is discussed. After storm rainfall, discharge increases rapidly, which is typical for karst springs. SEC displays a first maximum during the rising limb of the spring hydrograph, followed by a minimum indicating the arrival of freshly infiltrated water, often confirmed by increased levels of total organic carbon (TOC). The anomalous behaviour starts after this SEC minimum, when SEC rises again and remains elevated during the entire high-flow period, typically 20–40 µS/cm above the baseflow value. This is explained by variable catchment boundaries: When the water level in the aquifer rises, the catchment expands, incorporating zones of groundwater with higher SEC, caused by higher unsaturated zone thickness and subtle lithologic changes. This conceptual model has been checked by numerical investigations. A generalized finite-difference model including high-conductivity cells representing the conduit network (“discrete-continuum approach”) was set up to simulate the observed behaviour of the karst system. The model reproduces the shifting groundwater divide and the nearly simultaneous increase of discharge and SEC during high-flow periods. The observed behaviour is relevant for groundwater source protection zoning, which requires reliable delineation of catchment areas. Anomalous behaviour of SEC can point to variable catchment boundaries that can be checked by tracer tests during different hydrologic conditions.

Quaternary Paleoclimatology of the Black Sea basin, 1979, Schrader Hans Joachim,
The occurrence of polyhaline, mesohaline and oligohaline diatom, silicoflagellate, ebridian and chrysomonad populations in late Quaternary Black Sea sediments (DSDP Leg 42B) forms the basis for reconstruction of surface water paleosalinities in the Black Sea basin over the last 3 million years. Four major periods with increased salinites are separated by extended freshwater periods. Based on paleosalinites, indicators of trophic freshwater conditions and changes in diatom species diversity, a correlation is made to the northern Europian glacial--interglacial stratigraphy and this correlation is used to place paleoenvironmental events into a chronostratigraphy. The `synchronous' late Quaternary occurrence of sediments rich in organic carbon in both the Eastern Mediterranean and the Black Sea supports this interpretation.Three different stages in the interaction between the Black Sea and the Eastern Mediterranean Sea are defined: Stage A (exchange of freshwater and marine water similar to the present day flux) during the Holocene, Eemian, Holsteinian and Pliocene; Stage B (freshwater conditions with only occasional marine spills) during the Saalian, the Waalian, the Tiglian and the Praetiglian; and Stage C (freshwater conditions with no inflow of marine waters) during the Weichselian, the Elsterian and Eburonian

In Cave Oxidation of Organic Carbon and the Occurrence of Rainwater Inflow Cave Systems in the Seasonally Arid Lowland Tropics, 1987, Williamson, Kerry A.

Recent studies have shown that in cave oxidation of organic carbon can play a significant role in cave initiation and development. The production and flux of organic carbon in different seasonally arid and tropical karsts and in perpetually humid tropical karst is described, with particular consideration of the role of large particle size organic carbon. The model developed is used to explain the extent of rainwater inflow cave development and the apparent scarcity of such forms in the perpetually humid tropics plus arrested development in the seasonally arid sub-tropics.

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

Carbonate chemistry of surface waters in a temperate karst region: the southern Yorkshire Dales, UK, 1992, Pentecost Allan,
A detailed study of surface water chemistry is described from an important limestone region in northern England. Major ions and pH were determined for 485 sites (springs, seeps, streams, rivers and lakes) during summertime. The saturation state of the waters with respect to calcite was determined as the calcite saturation ratio ([Omega]). An unexpectedly large number of samples were found to be supersaturated (65.5% of the 268 km of watercourses surveyed). As a consequence, several streams entering major cave systems were incapable of further limestone solution, at least during periods of low flow. Many waters were supersaturated from their source and some deposited travertine. A significant negative correlation was found between spring discharge and both ([Omega]) and pH. Supersaturation was caused primarily by atmospheric degassing, with some contribution from aquatic plant photosynthesis.The median total dissolved inorganic carbon and Ca concentrations were 2.49 and 1.35 millimoles 1-1 respectively. Calcium originated exclusively from limestone, and carbon dioxide mainly from the soil and dissolved limestone. South facing catchments provided springwaters with significantly higher levels of TDIC and Ca when compared with north facing catchments. The study suggests that acid rain made a measurable contribution to limestone dissolution.Carboniferous limestone denudation rates were estimated as 54 to 63 m3 km-2 a-1 (54 to 63 mm 1000 years-1). About 50% of the Mg came from limestone and the remainder, together with most K, Na, SO4 and Cl from precipitation.Concentrations of dissolved nutrients were low, medians for NO3, NH4, total PO4 and SiO3 were 24 [mu]mol, 1.4 [mu]mol, 0.64 [mu]mol and 15.5 [mu]mol 1-1 respectively. The concentration of a further 23 trace elements was determined

Radiocarbon concentration and origin of thermal Karst waters in the region of the Bukk Mountains, northeastern Hungary, 1995, Hertelendi E. , Veres M. , Futo I. , Svingor E. , Miko L. , Lenart L. , Deak J. , Suveges M. ,
Karst springs are abundant in Hungary, and many are thermal (temperatures >30 degrees C). As thermal springs are a significant part of Hungary's water resources, it is important to quantify their travel times in the karst systems. Thus, we chose to measure T and delta(18)O in the water and delta(13)C and C-14 in dissolved inorganic carbon (DIC) in water from 50 thermal and nonthermal springs and wells in the Bukk Mountains, northeastern Hungary, Environmental isotope data confirm the karst waterflow pattern implied by earlier studies. We found the water in warm springs and boreholes to be mixtures of cold young and old thermal water. We also determined short mean-residence times for some large cold springs. The C-14 activities measured in these springs indicate that the recharge area of the karst aquifer is open to the atmosphere, and atmospheric CO2 contributes to the C-14 activity of these groundwaters. We observed good correlation between C-14 and H-3 activities and we determined negative correlations between C-14 concentration and delta(13)C values and temperature. From the delta(18)O values of the oldest thermal waters, we attribute their origin to precipitation during colder temperatures than at present

Aufeis of the Firth River basin, Northern Yukon Canada: Insights into permafrost hydrogeology and Karst, 1997, Clark Id, Lauriol B,
The 31-km(2) aufeis ice sheet of the upper Firth River holds a wealth of information on groundwater hydrology in periglacial environments. Baseflow recession calculations, corrected for aufeis storage (12% of basin discharge), indicate specific groundwater recharge rates of up to 100 mm yr(-1) (up to 50% of runoff), suggesting a significant proportion of drainage from karst. The upper Firth River aufeis is a composite aufeis, with discrete baseflow contributions from different watersheds. Since the late Pleistocene, annual growth of the aufeis has exerted a strong control on lateral erosion and the local river channel geomorphology. Two groundwater recharge processes are distinguished on the basis of carbonate geochemistry and 8(13)C: (1) Methanogenic groundwaters, with C-13(DIC) up to -3.3 parts per thousand, are recharged through saturated soils underlain by permafrost; conditions which support anaerobic consumption of dissolved organic carbon (DOC) and produce up to 700 mu g-CH4 L-1 (calculated), and (2) Karst groundwaters, with C-13-depleted DIC, recharged through unsaturated soils and circulate through fissured talik in the carbonate bedrock. Most drainage from the region shows varying contributions of these two groundwaters, although a greater contribution from the methanogenic groundwaters occurs in north-facing watersheds. The 8(13)C values far cryogenic calcite precipitates in the ice indicate that the karst groundwaters are the major contribution to aufeis growth. The combined use of 8(13)C(DIC) and geochemistry may be a useful tool to quantify methanogenesis in northern watersheds

Geochemical evolution of a karst stream in Devils Icebox Cave, Missouri, USA, 1997, Wicks Carol M. , Engeln Joseph F. ,
A 3.7 km flowpath along the main stream channel in Devils Icebox Cave, Boone County, Missouri, was sampled on 23 January, 23 March and 18 September 1994. In January 1994, the water was oversaturated with respect to both calcite and dolomite, and only minor compositional changes were observed along the flowpath. In March 1994, the water was oversaturated with respect to calcite but undersaturated with respect to dolomite. Using a mass-balance approach, the composition of the stream water at downstream locations was predicted by dissolution of dolomite (a maximum of 0.16 mmol s-1) and by a minor amount of calcite precipitation (a maximum of 0.03 mmol s-1). In September 1994, there were increases in the Mg, Ca, and total inorganic carbon (TIC) mass fluxes that were due to the dissolution of dolomite (SIdolomiteSI is saturation index) and calcite (SIcalcite2 of the water should decrease downstream; however, we found an increase in the partial pressure of CO2 along the stream. The source of this additional CO2 is thought to be microbial degradation of bat guano. The decomposition of bat guano appeared to change the composition of the stream water during the period the bats are in the cave, and this change was reflected in the composition of the stream water collected in September 1994. Based on the length of the flowpath and on the average velocity of the water along the flowpath, the travel time of water in this karst stream is less than 4 days. The reactions that control the chemistry of the karst water must be those with equally short characteristic times: the dissolution of dolomite and calcite, CO2 exchange, and microbial degradation of organic matter

Interactions between ground water and surface water in the Suwannee River Basin, Florida, 1997, Katz B. G. , Dehan R. S. , Hirten J. J. , Catches J. S. ,
Ground water and surface water constitute a single dynamic system in most parts of the Suwannee River basin due to the presence of karst features that facilitate the interaction between the surface and subsurface. Low radon-222 concentrations (below background levels) and enriched amounts of oxygen-18 and deuterium in ground water indicate mixing with surface water in parts of the basin. Comparison of surface water and regional ground water flow patterns indicate that boundaries for ground water basins typically do not coincide with surface water drainage subbasins. There are several areas in the basin where around water flow that originates outside of the Suwannee River basin crosses surface water basin boundaries during both low-flow and high-flow conditions. In a study area adjacent to the Suwannee River that consists predominantly of agricultural land use, 18 wells tapping the Upper Floridan aquifer and 7 springs were sampled three times during 1990 through 1994 for major dissolved inorganic constituents, trace elements, and nutrients. During a period of above normal rainfall that resulted in high river stage and high ground water levels in 1991, the combination of increased amounts of dissolved organic carbon and decreased levels of dissolved oxygen in ground water created conditions favorable for the natural reduction of nitrate by denitrification reactions in the aquifer. As a result, less nitrate was discharged by ground water to the Suwannee River

Spheroidal dolomites in a Visean karst system - Bacterial induced origin?, 1997, Nielsen P. , Swennen R. , Dickson J. A. D. , Fallick A. E. , Keppens E. ,
Spheroidal dolomite crystals occur in the karstified top of a Dinantian dolomite sequence in eastern Belgium. The spheroidal dolomite crystals are best developed at the base of the karst system. The dolomite crystals are characterized by a spherulitic or dumb-bell inclusion pattern, and are overgrown by dolomite cements with a rhombohedral outline. They are considered to be bacterially related precipitates based on, (1) textural similarities with documented bacteriogenic precipitates, (2) the presence of 'bacterial' microspheres and framboidal pyrite embedded within the dolomite, and (3) their general geological setting. The geochemical characteristics of the dolomites and associated minerals support a bacterial origin. The ubiquity of framboidal pyrite, depleted in S-34 (delta(34)S = - 22.4 to - 25.5 parts per thousand CDT), testifies to a period of bacterial sulphate reduction. The isotopic composition of the spheroidal dolomites (delta(13)C = - 2.4 to - 3.2 parts per thousand PDB and delta(18)O = - 3.8 to - 3.4 parts per thousand PDB) suggest a contribution from oxidized organic carbon produced during bacterial sulphate reduction. Sulphate reduction may also result in a concomitant O-18 depletion if the system is nearly closed. It is however, evident from the sulphur isotopic composition of associated framboidal pyrite that the system was fairly open. The O-18 depletion of the spheroidal dolomite crystals (delta(18)O = - 3.8 to - 3.4 parts per thousand PDB) and their occurrence adjacent to, and within karst cavities suggests a mixing zone origin, with a significant proportion of freshwater in it. The rhombohedral cement-overgrowths have calculated delta(18)O values in the range of 0 to 5.3 parts per thousand PDB, which reflect precipitation from normal to slightly evaporated contemporaneous seawater

Spatial and Temporal Variations in the Dissolved Organic Carbon Concentrations in the Vadose Karst Waters of Marengo Cave, Indiana, 1998, Toth, V. A.
In order to better understand the organic content of microbands in speleothems, seasonal variations in the organic concentrations of vadose drip waters were examined in relation to climatic and environmental variables. Seasonal variations in the organic concentrations of the vadose waters were observed by documenting the fluctuations of Dissolved Organic Carbon (DOC) and its corresponding fluorescence. Tracer dye tests established that the larger drips depositing calcite in Marengo Cave were fed by waters with a short residence time. A strong seasonal variation in DOC concentrations and natural fluorescence was detected at quickly responding sites. Slow, constant drip sites displayed a weaker seasonality. Further investigation is required to distinguish low fluorescing DOC and to determine if the same fluorophors identified in the vadose water can be identified in the organics trapped in the recipient calcite. The overall conclusions are that fluorescence is well correlated with DOC when the fluorescence range is high but it is not a strong indicator of DOC at low fluorescence values; that the value of fluorescence as a predictor of DOC may vary significantly with individual sampling sites; and that the highest fluorescence values occur in springtime and the weakest in summer and fall.

Kinetics and mechanisms of precipitation of calcite as affected by P-CO2 and organic ligands at 25 degrees C, 1998, Lebron I. , Suarez D. L. ,
This study was conducted to develop a model for the precipitation rate of calcite under varying CO2 partial pressures and concentrations of dissolved organic carbon (DOG). Precipitation rates of calcite were measured in solutions with supersaturation values (Omega) between 1 and 20 and in the presence of 2 m(2)L(-1) of calcite. Experiments were run at partial pressures of CO2 (P-CO2) in the range of 0.035-10 kPa and DOC concentrations in the range of 0.02-3.50 mM. The effects of these two variables were quantified separately for the precipitation mechanisms of crystal growth and heterogeneous nucleation. We found an increase in precipitation rate (at constant Omega) when P-CO2 increased. For constant Omega, we also found a linear relationship between calcite precipitation rate and activity of CaHCO3, indicating that CaHCO3 species have an active role in the mechanism of calcite precipitation. These findings suggest that the increase in the precipitation rate with higher P-CO2 levels is likely caused by the increase in the negative charge on the calcite surface together with an increase in the activity of CaHCO3 species in solution. The mechanism of inhibition of calcite crystal growth by organic ligands has been shown to be surface coating of the crystals by DOG. The amount of DOC adsorbed on the surface of the calcite crystals follows a Langmuir isotherm for all the P-CO2 levels studied; however, the amount of DOC necessary to inhibit calcite precipitation increased. With increasing P-CO2, the negative charge on the crystal increases, which affects crystal growth, but also these increases in P-CO2 cause a decrease in the solution pH and increase in the ionic strength for constant Omega. Solution pH and ionic strength affect the structure and degree of dissociation of the organic functional groups, which in turn affects the and DOC concentration on the inhibition of crystal growth and heterogeneous nucleation. The effect of P-CO2 and DOC concentration on the precipitation rate of calcite is expressed in a precipitation rate model which reflects the contributions of crystal growth and heterogeneous nucleation. Copyright (C) 1998 Elsevier Science Ltd

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

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)

Depositional Facies and Aqueous-Solid Geochemistry of Travertine-Depositing Hot Springs (Angel Terrace, Mammoth Hot Springs, Yellowstone National Park, U.S.A.), 2000, Fouke Bw, Farmer Jd, Des Marais Dj, Pratt L, Sturchio Nc, Burns Pc, Discipulo Mk,
Petrographic and geochemical analyses of travertine-depositing hot springs at Angel Terrace, Mammoth Hot Springs, Yellowstone National Park, have been used to define five depositional facies along the spring drainage system. Spring waters are expelled in the vent facies at 71 to 73{degrees}C and precipitate mounded travertine composed of aragonite needle botryoids. The apron and channel facies (43-72{degrees}C) is floored by hollow tubes composed of aragonite needle botryoids that encrust sulfide-oxidizing Aquificales bacteria. The travertine of the pond facies (30-62{degrees}C) varies in composition from aragonite needle shrubs formed at higher temperatures to ridged networks of calcite and aragonite at lower temperatures. Calcite 'ice sheets', calcified bubbles, and aggregates of aragonite needles ('fuzzy dumbbells') precipitate at the air-water interface and settle to pond floors. The proximal-slope facies (28-54{degrees}C), which forms the margins of terracette pools, is composed of arcuate aragonite needle shrubs that create small microterracettes on the steep slope face. Finally, the distal-slope facies (28-30{degrees}C) is composed of calcite spherules and calcite 'feather' crystals. Despite the presence of abundant microbial mat communities and their observed role in providing substrates for mineralization, the compositions of spring-water and travertine predominantly reflect abiotic physical and chemical processes. Vigorous CO2 degassing causes a unit increase in spring water pH, as well as Rayleigh-type covariations between the concentration of dissolved inorganic carbon and corresponding {delta}13C. Travertine {delta}13C and {delta}18O are nearly equivalent to aragonite and calcite equilibrium values calculated from spring water in the higher-temperature ([~]50-73{degrees}C) depositional facies. Conversely, travertine precipitating in the lower-temperature (<[~]50{degrees}C) depositional facies exhibits {delta}13C and {delta}18O values that are as much as 4{per thousand} less than predicted equilibrium values. This isotopic shift may record microbial respiration as well as downstream transport of travertine crystals. Despite the production of H2S and the abundance of sulfide-oxidizing microbes, preliminary {delta}34S data do not uniquely define the microbial metabolic pathways present in the spring system. This suggests that the high extent of CO2 degassing and large open-system solute reservoir in these thermal systems overwhelm biological controls on travertine crystal chemistry

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