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Speleology in Kazakhstan

Shakalov on 04 Jul, 2018
Hello everyone!   I pleased to invite you to the official site of Central Asian Karstic-Speleological commission ("Kaspeko")   There, we regularly publish reports about our expeditions, articles and reports on speleotopics, lecture course for instructors, photos etc. ...

New publications on hypogene speleogenesis

Klimchouk on 26 Mar, 2012
Dear Colleagues, This is to draw your attention to several recent publications added to KarstBase, relevant to hypogenic karst/speleogenesis: Corrosion of limestone tablets in sulfidic ground-water: measurements and speleogenetic implications Galdenzi,

The deepest terrestrial animal

Klimchouk on 23 Feb, 2012
A recent publication of Spanish researchers describes the biology of Krubera Cave, including the deepest terrestrial animal ever found: Jordana, Rafael; Baquero, Enrique; Reboleira, Sofía and Sendra, Alberto. ...

Caves - landscapes without light

akop on 05 Feb, 2012
Exhibition dedicated to caves is taking place in the Vienna Natural History Museum   The exhibition at the Natural History Museum presents the surprising variety of caves and cave formations such as stalactites and various crystals. ...

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That saltation load is the solid matter transported by streams [16].?

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Featured articles from Cave & Karst Science Journals
Chemistry and Karst, White, William B.
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Karst environment, Culver D.C.
Mushroom Speleothems: Stromatolites That Formed in the Absence of Phototrophs, Bontognali, Tomaso R.R.; D’Angeli Ilenia M.; Tisato, Nicola; Vasconcelos, Crisogono; Bernasconi, Stefano M.; Gonzales, Esteban R. G.; De Waele, Jo
Calculating flux to predict future cave radon concentrations, Rowberry, Matt; Marti, Xavi; Frontera, Carlos; Van De Wiel, Marco; Briestensky, Milos
Microbial mediation of complex subterranean mineral structures, Tirato, Nicola; Torriano, Stefano F.F;, Monteux, Sylvain; Sauro, Francesco; De Waele, Jo; Lavagna, Maria Luisa; D’Angeli, Ilenia Maria; Chailloux, Daniel; Renda, Michel; Eglinton, Timothy I.; Bontognali, Tomaso Renzo Rezio
Evidence of a plate-wide tectonic pressure pulse provided by extensometric monitoring in the Balkan Mountains (Bulgaria), Briestensky, Milos; Rowberry, Matt; Stemberk, Josef; Stefanov, Petar; Vozar, Jozef; Sebela, Stanka; Petro, Lubomir; Bella, Pavel; Gaal, Ludovit; Ormukov, Cholponbek;
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Your search for isotope fractionation (Keyword) returned 10 results for the whole karstbase:
Several kinds of base metal deposits occur in the lower Paleozoic of southwest Sardinia (Iglesiente-Sulcis mineral district). This paper deals with those deposits which are generally referred to as Permo-Triassic, because they accompany and postdate the Hercynian orogeny and are related to magmatic activity. A large number of previously published geochemical data, integrated with additional new data (Sr, Pb, O, C, and S isotopes), are reviewed and discussed in the frame of the late to post-Hercynian geologic evolution of southwest Sardinia. According to geological and mineralogical characteristics, three types of deposits can be distinguished: (1) skarn ores related to late Hercynian leucogranitic intrusions, (2) high-temperature veins, and (3) low-temperature veins and karst filling. Pervasive epigenetic dolomitization phenomena are geochemically related to the low-temperature deposits. Sr and Pb isotopes of the first and second types (0.7097-0.7140 Sr-87/Sr-86; 17.97-18.29 Pb-206/Pb-204; 38.11-38.45 Pb-208/Pb-204) are distinctly more radiogenic than those of the third type (0.7094-0.7115 Sr-87/Sr-86; 17.86-18.05 Pb-206/Pb-204; 37.95-38.19 Pb-208/Pb-204) which, in turn, are closer to Paleozoic ores and carbonates. Fluid inclusion data indicate that the fluids responsible for mineralization of the first and second types of deposits were hot and dilute (T(h)= 370-degrees-140-degrees-C; <5 wt % NaCl equiv). In contrast, relatively colder and very saline fluids (T(h)= 140-degrees-70-degrees-C; >20 wt % NaCl equiv) were responsible for the third type of mineralization, as well for epigenetic dolomitization of the Cambrian host rocks. O isotopes measured in minerals from the first two types (deltaO-18SMOW = 12.8-18.9 parts per thousand) are O-18 depleted with respect to the third type (deltaO-18SMOW = 15.9-22.1 parts per thousand). These data, coupled with fluid inclusion formation temperatures, indicate that the fluids responsible for the first two types of mineralization were O-18 enriched with respect to those of the third type and related hydrothermal phenomena. The deltaS-34CDT in sulfides of the first two types vary between 3.7 and 10.73 per mil, whereas the values of the third type range from 12.0 to 17.9 per mil. Late to post-Hercynian mineralization is thus explained as the result of three distinct, though partly superimposed, hydrothermal systems. System 1 developed closer to the late Hercynian leucogranitic intrusions and led to the formation of the first and subsequently the second type of mineralization. The relatively hot and diluted fluids had a heated meteoric, or even partly magmatic, origin. Metals were leached from an external, radiogenic source, represented either by Hercynian leucogranites or by Paleozoic metasediments. Sulfur had a partly magmatic signature. System 2 was characterized by very saline, colder fluids which promoted dolomitization, silicification, and vein and karst mineralization. These fluids share the typical characteristics of formation waters, even though their origins remain highly speculative. The hydrothermal system was mainly rock dominated, with only a minor participation of the external radiogenic source of metals. Sulfur was derived by recirculation of pre-Hercynian strata-bound ores. System 3 records the invasion of fresh and cold meteoric waters which precipitated only minor ore and calcite gangue. It may represent the further evolution of system 2, possibly spanning a time well after the Permo-Triassic. The timing of all these phenomena is still questionable, due to the poor geologic record of the Permo-Triassic in southwest Sardinia. Nevertheless, the hypothesized scenario bears many similarities with hydrothermal processes documented throughout the Hercynian in Europe and spanning the same time interval. A comparison with the latter mineralization and hydrothermal activities leads to the hypothesis that the first two types of mineralization are linked to late Hercynian magmatic activity, whereas the third type may be related to either strike-slip or tensional tectonics which, throughout Europe mark the transition from the Hercynian orogeny to the Alpine cycle

Controls on bacterial sulphate reduction in a dual porosity aquifer system: the Lincolnshire Limestone aquifer, England, 2000, Bottrell Sh, Moncaster Sj, Tellam Jh, Lloyd Jw, Fisher Qj, Newton Rj,
Chemical and sulphur isotopic analyses are presented of fissure-waters and pore-waters in the deep confined zone of a dual porosity carbonate aquifer. Some of the fissure-waters show good evidence for bacterial sulphate reduction, with low concentrations of sulphide present which is strongly to moderately depleted in 34S relative to sulphate. The sulphur geochemistry is best interpreted as mixing between: (i) a reduced water with sulphide ~60[per mille sign] depleted in 34S relative to sulphate; and (ii) a sulphate-rich water from up-dip in the aquifer. In addition, sulphide oxidation occurs where sufficiently oxidizing water is drawn in by abstractions. The large isotope fractionation factor associated with the sulphidic waters is probably the result of redox cycling of sulphur with little net reduction, rather than a true kinetic fractionation factor. By contrast, pore-waters in the 'sulphate reducing zone' show little or no evidence for the effects of sulphate reduction, despite the fact that the pore-waters represent a significant reservoir of sulphate for reduction. Some pore-waters have been modified recognizably by diffusional exchange with the fissure-waters, but the aquifer matrix has not been colonized by sulphate reducing bacteria, probably because porethroats in the limestone are too small for bacteria to pass. Physical exclusion of bacteria from the aquifer matrix and limited diffusional exchange are likely to exert fundamental controls on bacterial redox processes in dual porosity aquifer systems and other systems with low permeability due to small pore interconnections

C and O stable isotope variability in recent freshwater carbonates (River Krka, Croatia), 2004, Lojen S. , Dolenec T. , Vokal B. , Cukrov N. , Mihelcic G. , Papesch W. ,
Three types of recent carbonate precipitates from the River Krka, Croatia, were analysed: (1) bulk tufa from four main cascades in a 34 km long section of the river flow through the Krka National Park; (2) a laminar stromatolite-like incrustation formed in the tunnel of a hydroelectric power plant close to the lowest cascade; and (3) recent precipitates collected on artificial substrates during winter, spring and summer periods. Stable isotope compositions of carbon (delta(13)C) and oxygen (delta(18)O) in the carbonate and organic carbon (delta(13)C(org)) were determined and compared with delta(18)O of water and delta(13)C of dissolved inorganic carbon (DIC). The source of DIC, which provides C for tufa precipitation, was determined from the slope of the line ([DIC]/[DIC0]-1) vs. (delta(13)C-DIC x ([DIC]/[DIC0])) (Sayles & Curry, 1988). The delta(13)C value of added DIC was -13.6parts per thousand, corresponding to the dissolution of CO2 with delta(13)C between -19.5 and -23.0parts per thousand Vienna Pee Dee Belemnite (VPDB). The observed difference between the measured and calculated equilibrium temperature of precipitation of bulk tufa barriers indicates that the higher the water temperature, the larger the error in the estimated temperature of precipitation. This implies that the climatic signals may be valid only in tufas precipitated at lower and relatively stable temperatures. The laminar crust comprising a continuous record of the last 40 years of precipitation shows a consistent trend of increasing delta(13)C and decreasing delta(18)O. The lack of covariation between delta(13)C and delta(18)O indicates that precipitation of calcite was not kinetically controlled for either of the elements. delta(13)C and delta(18)O of precipitates collected on different artificial substrates show that surface characteristics both of substrates and colonizing biota play an important role in C and O isotope fractionation during carbonate precipitation

Isotope records in submarine speleothems from the Adriatic coast, Croatia, 2005, Suric Masa, Horvatincic Nada, Suckow Axel, Juracic Mladen, Baresic Jadranka,
Isotope studies, using 14C dating, {delta}13C and {delta}18O measurements, were performed at eight speleothems taken from three submerged caves situated along the eastern Adriatic coast, Croatia. The speleothems were taken from 17 m to 38.5 m depth below mean sea level. The samples consist of four stalagmites and four stalactites in position of growth, covered with marine biogenic overgrowth, and the length of speleothems ranges from ~80 mm to ~190 mm. The youngest (surface) and the oldest (base) layers of speleothems were radiocarbon dated and the 14C ages range from 21,600 cal B.P. to 37,000 yr B.P. During that period the global sea level was more than 40 m below the recent one, so presently submerged objects were under the subaerial conditions necessary for speleothem deposition. 14C ages of the youngest layer range from 21,600 to 32,200 cal B.P. for different submerged speleothems. This indicates the time when the speleothem growth ceased, most probably due to flooding of the cave with either fresh or brackish water. Speleothem growth during the Last Glacial Maximum (30-19 kyr ago) and different time of growth cessation for the different speleothem samples suggest that climate change was not the reason for cessation of deposition. Samples for {delta}13C and {delta}18O measurements were taken from six submerged speleothems with sampling distances of ca. 5-10 mm from the surface to the base of speleothems. Most of the {delta}13C values are in the range from -10.5{per thousand} to -8.5{per thousand}, with few exceptions to -6{per thousand}. These values are typical for Dinaric karst, and very different values for marine biogenic overgrowth indicate that no isotopic exchange took place during the submerged period. {delta}18O values range from -6.7{per thousand} to -4.1{per thousand}. A weak correlation between {delta}13C and {delta}18O values indicates possible kinetic isotope fractionation during the calcite precipitation. If the {delta}18O record is interpreted as climatic signal, it suggests similar climatic conditions for the late Pleistocene and the Holocene, especially no significant differences in temperature and/or moisture transport

The Upper Valanginian (Early Cretaceous) positive carbonisotope event recorded in terrestrial plants, 2005, Grocke D. R. , Price G. D. , Robinson S. A. , Baraboshkin E. Y. , Mutterlose J. , Ruffell A. H.

Our understanding of the ancient ocean-atmosphere system has focused on oceanic proxies. However, the study of terrestrial proxies is equally necessary to constrain our understanding of ancient climates and linkages between the terrestrial and oceanic carbon reservoirs. We have analyzed carbon–isotope ratios from fossil plant material through the Valanginian and Lower Hauterivian from a shallow-marine, ammonite-constrained succession in the Crimean Peninsula of the southern Ukraine in order to determine if the Upper Valanginian positive carbon–isotope excursion is expressed in the atmosphere.d 13 Cplantvalues fluctuate around 23xto 22xfor the Valanginian–Hauterivian, except during the Upper Valanginian where d 13 C plantvalues record a positive excursion to ~ 18x. based upon ammonite biostratigraphy from Crimea, and in conjunction with a composite Tethyan marined 13 Ccarb curve, several conclusions can be drawn: (1) thed 13 Cplantrecord indicates that the atmospheric carbon reservoir was affected; (2) the defined ammonite correlations between Europe and Crimea are synchronous; and (3) a change in photosynthetic carbon–isotope fractionation, caused by a decrease in atmosphericpCO2, occurred during the Upper Valanginian positived 13 C excursion. Our new data, combined with other paleoenvironmental and paleoclimatic information, indicate that the Upper Valanginian was a cool period (icehouse) and highlights that the Cretaceous period was interrupted by periods of cooling and was not an equable climate as previously thought.

Modification and preservation of environmental signals in speleothems, 2006, Fairchild Ij, Smith Cl, Baker A, Fuller L, Spotl C, Mattey D, Mcdermott F, Eimp,
Speleothems are primarily studied in order to generate archives of climatic change and results have led to significant advances in identifying and dating major shifts in the climate system. However, the climatological meaning of many speleothem records cannot be interpreted unequivocally, this is particularly so for more subtle shifts and shorter time periods, but the use of multiple proxies and improving understanding of formation mechanisms offers a clear way forward. An explicit description of speleothem records as time series draws attention to the nature and importance of the signal filtering processes by which the weather, the seasons, and longer-term climatic and other environmental fluctuations become encoded in speleothems. We distinguish five sources of variation that influence speleothem geochemistry, i.e. atmospheric, vegetation/soil, karstic aquifer, primary speleothem crystal growth and secondary alteration, and give specific examples of their influence. The direct role of climate diminishes progressively through these five factors. We identify and review a number of processes identified in recent and current work that bear significantly on the conventional interpretation of speleothem records, for example: (1) speleothem geochemistry can vary seasonally and hence a research need is to establish the proportion of growth attributable to different seasons and whether this varies over time; (2) whereas there has traditionally been a focus on monthly mean delta O-18 data of atmospheric moisture, current work emphasizes the importance of understanding the synoptic processes that lead to characteristic isotope signals, since changing relative abundance of different weather types might control their variation on the longer-term; (3) the ecosystem and soil zone overlying the cave fundamentally imprint the carbon and trace element signals and can show characteristic variations with time; (4) new modelling on aquifer plumbing allows quantification of the effects of aquifer mixing; (5) recent work has emphasized the importance and seasonal variability Of CO2-degassing leading to calcite precipitation upflow of a depositional site on carbon isotope and trace element composition of speleothems; (6) although much is known about the chemical partitioning between water and stalagmites, variability in relation to crystal growth mechanisms and kinetics is a research frontier; (7) aragonite is susceptible to conversion to calcite with major loss of chemical information, but the controls on the rate of this process are obscure. Analytical factors are critical in generating high-resolution speleothem records. A variety of methods of trace element analysis is available, but standardization is a common problem with the most rapid methods. New stable isotope data on Irish stalagmite CC3 compares rapid laser-ablation techniques with the conventional analysis of micromilled powders and ion microprobe methods. A high degree of comparability between techniques for delta O-18 is found on the millimeter to centimeter scale, but a previously described high-amplitude oxygen isotope excursion around 8.3 ka is identified as an analytical artefact related to fractionation of the laser-analysis associated with sample cracking. High-frequency variability of not less than 0.5 parts per thousand may be an inherent feature of speleothem delta O-18 records. (c) 2005 Elsevier B.V. All rights reserved

Pleistocene speleothems of Mallorca: implications for palaeoclimate and carbonate diagenesis in mixing zones, 2006, Csoma Ae, Goldstein Rh, Pomar L,
The Pleistocene speleothems of Sa Bassa Blanca cave, Mallorca, are excellent indicators of palaeoclimate variations, and are samples that allow evaluation of the products and processes of mixing-zone diagenesis in an open-water cave system. Integrated stratigraphic, petrographic and geochemical data from a horizontal core of speleothem identified two main origins for speleothem precipitates: meteoric-marine mixing zone and meteoric-vadose zone. Mixing-zone precipitates formed at and just below the water-air interface of cave pools during interglacial times, when the cave was flooded as a result of highstand sea-level. Mixing-zone precipitates include bladed and dendritic high-Mg calcite, microporous-bladed calcite with variable Mg content, and acicular aragonite; their presence suggests that calcium-carbonate cementation is significant in the studied mixing-zone system. Fluid inclusion salinities, delta(13)C and delta(18)O compositions of the mixing-zone precipitates suggest that mixing ratio was not the primary control on whether precipitation or dissolution occurred, rather, the proximity to the water table and degassing of CO2 at the interface, were the major controls on precipitation. Thus, simple two-end-member mixing models may apply only in mixing zones well below the water table. Meteoric-vadose speleothems include calcite and high-Mg calcite with columnar and bladed morphologies. Vadose speleothems precipitated during glacial stages when sea level was lower than present. Progressive increase in delta(13)C and delta(18)O of the vadose speleothems resulted from cooling temperatures and more positive seawater delta(18)O associated with glacial buildup. Such covariation could be considered as a valid alternative to models predicting invariant delta(18)O and highly variable delta(13)C in meteoric calcite. Glacio-eustatic oscillations of sea-level are recorded as alternating vadose and mixing-zone speleothems. Short-term climatic variations are recorded as alternating aragonite and calcite speleothems precipitated in the mixing zone. Fluid-inclusion and stable-isotope data suggest that aragonite, as opposed to calcite, precipitated during times of reduced meteoric recharge


Nanisivik (Inuit – “the place where they find things’) zinc/lead mine is located at Lat. 73o N in northwestern Baf?n Island. The host rock is a Proterozoic platform carbonate 260-800 m thick, medium to massively bedded and pervasively dolomitized. It rests on mixed shales and shaly dolomites, and is overlain by 150+ m of further shales functioning as an aquitard. These formations were buried by later Proterozoic strata, uplifted, eroded and buried again in a Cambrian sedimentary basin. The ore-grade deposits are contained within a horst block of the dolomites dipping NW at 15o across it. Graben to the north and south are roofed in the overlying shales. The principal deposit, the Main Ore, is of zinc, lead and iron sul?de precipitates plus gangue minerals, chie?y secondary dolomite. It extends for three km E-W along the horst. It is horizontal, at ~300 m above sea level and terminated at both ends by modern valley entrenchments. The Main Ore body is consistently ~100 m in width and ?ve-seven m in depth. This wide ceiling is a nearly planar, horizontal corrosion bevel. The sulfdes scarcely extend above it anywhere. Within the Main Ore two or more generations of tapered ?ns of dolomite in situ extend from both south (updip) and north (downdip) walls into the cavity. Fin surfaces truncate the bedding. Edges of ?ns are sinuous, some meandering with a wavelength of ~50 m. Very sharp, horizontal corrosion notches 20-30 cm high extend into the dolomite walls for at least 20 m (the limit of deep crosscuts in the mine). They are ?lled with layered pyrites which continue out into the ore body as regular sheets truncating earlier, dipping mineral layers until they themselves are truncated by later fillings. One exceptional notch, one meter deep, is at least 350 m in breadth. The ore displays four sedimentary modes: (i) regular layers settled or precipitated onto the cavity floor; (ii) chaotic polymict breccias suggestive of channel cut-and-?ll episodes; (iii) the horizontal pyrite sheets in corrosion notches; (iv) minor metasomatic replacements of dolomite. The ore cavity was created by paragenesis in a channel ?ow mode, with ore and gangue deposition on the floor taking place in tandem with dissolutional cavity creation upwards,. Principal deposition took place when a fluid interface could be rigorously maintained. Fluid inclusions indicate derivation of the metals from exchange reactions with metalliferous sediments (the underlying shales), indicating low water/rock ratios and moderate temperatures. The ore fluids were similar to oil field brines. Sulfur isotope fractionations indicate temperatures of 90-150 +/-40o C, suggesting that the Main Ore formed along a gas/brine interface at a depth of at least 1600 m as a consequence of ?uid expulsion in the subsiding Cambrian sedimentary basin.

U-series dating and isotope geochemical study of the Gellrt Hill (Budapest) travertine, 2009, Kele S. , Scheuer G. , Demny A. , Shen Ch. C. , Chiang H. W.

Travertine is quite a common formation in the area of Budapest (Hungary) indicating strong hydrothermal activity during the Pliocene and Quaternary. It covers former terraces of the Danube River and older geomorphologic horizons; thus, it is an important archive to date fluvial terraces and tectonic movements. Despite numerous investigations performed on these deposits, only few radiometric data are available so far and the absence of the exact timing information hindered paleoclimatic interpretation. The area of Gellért Hill consists mainly of Upper Triassic dolomite, but Quaternary travertine can also be found. In this study a detailed petrographic and stable isotope geochemical study of four travertine sites (1. Ifjúsági Park; 2. Számadó u. (Street); 3. Kelenhegyi u. (Street); 4. Somlói u. (Street)) of the Gellért Hill area is presented, along with analyses on the recent carbonate deposits of Gellért Hill and Sárosfürdõ. The travertine of Ifjúsági Park and Számadó u. are spring cone deposits, while the travertine of the Kelenhegyi u. represents a shallow-water depositional environment. based on the paleontological studies of Jánossy (in Scheuer and Schweitzer, 1988) the Gellért Hill travertine was thought to have been formed during the Lower Pleistocene; however, no radiometric age dating had been performed on these deposits prior our study. Our U/Th analyses yielded ages of 250±44 ky for the Ifjúsági Park travertine (220 m asl) and 180±49 ky for the Számadó u. travertine (195 m asl). These new U/Th ages are in contradiction with the previously assumed Lower Pleistocene age, implying gradual relative decrease in the paleokarst water-level and proving that the elevation of the individual travertine deposits not necessarily show their relative age. The uplift rates of Gellért Hill calculated from the U/Th age data and elevation of travertine occurrences range between 0.47 and 0.52 mm/yr, which is significantly higher than the uplift rates calculated for the Rózsadomb area (0.20 0.25 mm/yr; Kele et al., submitted). The difference in the incision rates between the individual sub-areas suggests that selective uplift was characteristic for the Buda Hills during the Middle Pleistocene; thus, up-scaling reconstruction of paleokarst waterlevel for the whole area from a given locality is not possible. Oxygen isotope analyses of recent carbonate deposits of Gellért Hill, Sárosfürdõ and Rudas Spa revealed that these calcites precipitated under non-equilibrium conditions, and the measured calcitewater oxygen isotope fractionation show the same positive shift relative to "equilibrium values" as was observed in the case of the recently-forming Egerszalók travertine (Kele et al. 2008). Assuming that the water of the paleo-springs of Gellért Hill derived from precipitation infiltrated during interstadial periods of the Pleistocene and considering non-equilibrium deposition (i.e. using the empirical calcite-water oxygen isotope fractionation of Kele et al. 2008), their calculated paleotemperature could range between 22 (±4) °C and 49 (±6) °C. based on the 18Otravertine differences the Ifjúsági Park and the Számadó u. spring cone type travertine was deposited from the highest temperature water, while from the lowest temperature water the travertine of Kelenhegyi u. was formed.

Empirical equations for the temperature dependence of calcite-water oxygen isotope fractionation from 10 to 708C, 2010, Demeґny A. , Kele S. , Sikloґsy Z.

Although the temperature dependence of calcite-water oxygen isotope fractionation seems to have been well established by numerous empirical, experimental and theoretical studies, it is still being discussed, especially due to the demand for increased accuracy of paleotemperature calculations. Experimentally determined equations are available and have been verified by theoretical calculations (considered as representative of isotopic equilibrium); however, many natural formations do not seem to follow these relationships implying either that existing fractionation equations should be revised, or that carbonate deposits are seriously affected by kinetic and solution chemistry effects, or late-stage alterations. In order to test if existing fractionation-temperature relationships can be used for natural deposits, we have studied calcite formations precipitated in various environments by means of stable isotope mass spectrometry: travertines (freshwater limestones) precipitating from hot and warm waters in open-air or quasi-closed environments, as well as cave deposits formed in closed systems. Physical and chemical parameters as well as oxygen isotope composition of water were monitored for all the investigated sites. Measuring precipitation temperatures along with oxygen isotope compositions of waters and calcites yielded empirical environment-specific fractionation– temperature equations: [1] 1000 _ lnaј17599/T – 29.64 [for travertines with a temperature range of 30 to 70-C] and [2] 1000 _ lnaј17500/T – 29.89 [for cave deposits for the range 10 to 25-C]. Finally, based on the comparison of literature data and our results, the use of distinct calcite-water oxygen isotopic fractionation relationships and application strategies to obtain the most reliable paleoclimate information are evaluated.

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