Isotopic composition (H,O, Cl,Sr) of ground brines of the Siberian Platform

New data on the geochemistry and isotopic composition of chloride brines of the Siberian Platform are presented. The distribution of stable isotopes (²H, ¹⁸O, and ³⁷Cl) in brines of the Tunguska, Angara-Lena, western part of the Yakutian and Olenek artesian basins and ⁸⁷Sr/⁸⁶Sr in brines of the western part of the Olenek artesian basin was studied in the context of the problem of genesis of highly mineralized groundwaters. Results of the study and comparative analysis of the geochemical and isotopic peculiarities of the Siberian Platform brines conform to the theory of brine formation through the interaction of connate waters with enclosing rocks.     

Hydrochemical characteristics and controlling factors for waters’ chemical composition in the Tarim Basin,Western China

This paper covers the chemical and isotopic composition of river water, groundwater from wells (15–25 m), saline spring water and stagnant surface water providing evidence for controlling factors of water composition and water evolution process in the Tarim Basin, Xinjiang, western China. Analytical data for major and minor ions of totaling 537 water samples were obtained from both years of teamwork and old reference materials. It is found that the ion background value ratio SO₄/Cl for river water (2.75) of the Tarim Basin is two times higher than that of the Qaidam Basin (0.88) and 18 times higher than seawater (0.14); K/Cl of these two basins (0.06 and 0.07) are all two times higher than seawater (0.02). This reveals that material sources of Lop Nur are relatively richer in potassium and sulfate, while poorer in chloride. Gradual changes of stable isotopic compositions in waters clearly indicate the effect of evaporation on water evolution of the basin. Besides evaporation and weathering of surrounding rocks, wide distribution of chloride type water, which commonly exist in saline springs/brines and seldom exist in other waters, indicates that hydrothermal Ca–Cl brines discharged from deep within the earth join water evolution of the basin.     

Geochemistry of ground ice,saline groundwater,and brines in the cryoartesian basins of the northeastern Siberian Platform

We present results of a comprehensive study of ground ice, saline waters, and brines in the cryoartesian basins of the northeastern Siberian Platform. The composition of major geochemical types of ground ice is considered. The specifics of the hydrogeochemical zonation of the cryoartesian basins are the regional distribution of chloride saline waters and brines. Study of stable isotopes (¹⁸O, D, ³⁷Cl, ⁸¹Br, and ⁸⁷Sr/⁸⁶Sr) led us to the conclusion that the chloride brines resulted either from the leaching of halogen rocks or from the metamorphism of bittern connate water. The drainage brine reserves (hydromineral resources) of the Udachnaya kimberlite pipe in the Olenek cryoartesian basin are assessed.     

The behavior of lithium and its isotopes in oilfield brines: evidence from the Heletz-Kokhav field, Israel

Twenty-four brine samples from the Heletz-Kokhav oilfield, Israel, have been analyzed for chemical composition and Li isotope ratios. The chemical composition of the brines, together with geological evidence, suggests derivation from (Messinian) seawater by evaporation that proceeded well into the gypsum stability field but failed to reach the stage of halite crystallization. The present salinity of the samples (18-47 g Cl/L) was achieved by dilution of the original evaporitic brine by local fresh waters. Like brines from other sedimentary basins, the Li/Cl ratios in the Heletz-Kokhav samples show a prominent Li enrichment (five-fold to eight-fold) relative to modern seawater. The isotopic ratios of Li, expressed in the δ ⁶Li notation, vary from −26.3 to −17.9‰, all values being significantly higher than that of modern seawater (−32‰) irrespective of their corresponding Li concentration (1.0-2.3 mg/L). The isotopic composition of Li and the Li/Cl ratio in the oilfield brines were acquired in two stages: (a) The original evaporated seawater gained isotopically light Li during the diagenetic interaction between the interstitial Messinian brine and the basin sediments. A parent brine with an elevated Li/Cl ratio was formed. The brine was later diluted in the oilfields. (b) The δ ⁶Li values of the final brines were determined during epigenetic interaction with the Heletz-Kokhav aquifer rocks. At the same time, the Li/Cl ratio inherited from stage (a) remained largely unchanged. This work represents the first use of lithium isotopic composition to elucidate the origin and evolution of formation waters in sedimentary basins.     

Palaeohydrodynamics of fluids in the Brent Group (Oseberg Field,Norwegian North Sea) from chemical and isotopic compositions of formation waters

Generally, the history of past sub-surface fluid movements is difficult to reconstruct. However, the composition of oil-field waters characterizes the origins and mixing processes that allow such a reconstruction. We have investigated present-day formation waters from Brent Group sedimentary rocks of the Oseberg Field in order to assess both their geochemical variations, and their origin(s). Water samples (sampled at the separator) produced from immediately above the oil–water contact and from the aquifer (water-saturated zone below the oil–water contact) were taken from 11 wells across the field. In addition, 3 trace water samples were extracted from oil produced from higher up in the oil column. The water samples were analysed for their chemical components and isotopic compositions. Conservative tracers such as Cl, Br, δD, and δ¹⁸O were used to evaluate the origin of the waters. All formation waters can be characterised as Na–Cl-brines. The separator samples are of aquifer origin, indicating that aquifer water, drawn up by the pressure reduction near the well, is produced from the lower few tens of metres of the oil-zone. By defining plausible endmembers, the waters can be described as mixtures of seawater (60–90%), meteoric water (10–30%), evaporated seawater (primary brines) (3–5%), and possibly waters which have dissolved evaporites (secondary brines). Alternatively, using multidimensional scaling, the waters can be described as mixtures of only 3 endmembers without presupposing their compositions. In fact, they are seawater, very dilute brine, and a secondary brine (confirming the power of this approach). Meteoric water was introduced into the reservoir during the end-Brent and early-Cretaceous periods of emergence and erosion, and partially replaced the marine pore fluids. Lateral chemical variations across the Oseberg Field are extremely small. The waters from closer to the erosion surfaces show slightly stronger meteoric water isotopic signatures. The primary and secondary brines are believed to come from Permian and Triassic evaporitic rocks in the deeply buried Viking Graben to the west, and to have been modified by water–rock interactions along their migration path. These primary basinal brines have not been detected in the oil–zone waters, suggesting that the brines entered the reservoir after the main phase of oil-migration. There are indications that these external fluids were introduced into the reservoir along faults. Present-day aquifer waters are mixtures of waters from different origins and hardly vary at a field-scale. They are different in composition to the water trapped in the present oil-zone. One of the oil-zone samples is a very dilute brine. It is thought to represent a simple mixture of seawater and meteoric water. Due to oil-emplacement, this geochemical signature was preserved in the waters trapped within the oil-zone. Another oil-zone water shows a very similar chemical signature to the aquifer waters, but the chlorine isotopic signature is similar to that of the dilute oil-zone water. This water is interpreted to represent a palaeo-aquifer water. That is, it was within the aquifer zone in the past, but was trapped by subsequent emplacement of more oil. These vertical differences can be explained by two features: (i) emergence of the Brent Group sedimentary rocks in the Early Cretaceous allowed ingress of meteoric water; (ii) subsequent rapid burial of Viking Graben rocks caused migration of petroleum and aqueous fluids into the adjacent, less deeply buried Oseberg Field.     

Brines in the Carboniferous Sydney Coalfield,Atlantic Canada

Formation waters within Upper Carboniferous sandstones in the sub-sea Prince and Phalen coal mines, Nova Scotia, originated as residual evaporative fluids, probably during the precipitation of Windsor Group (Lower Carboniferous) salts which underlie the coal measures. Salinity varies from 7800 to 176,000 mg/l, and the waters are Na–Ca–Cl brines enriched in Ca, Sr and Br and depleted in Na, K, Mg and SO₄ relative to the seawater evaporation curve. Br:Cl and Na:Cl ratios suggest that the brine composition corresponds to an evaporation ratio of as much as 30. The brines lie close to the meteoric line on H/O isotopic plots but with a compositional range of δ¹⁸O from −4.18 to −6.99 and of δD from −42.4 to −23.5, distant from modern meteoric or ocean water. Mine water composition contrasts with that of nearby salt-spring brines, which are inferred to have originated through dissolution of Windsor Group evaporites by modern meteoric waters. However, a contribution to the mine waters from halite dissolution and from Br in organic matter cannot be ruled out. Present concentrations of several elements in the brines can be explained by water–rock interaction. The original Windsor brines probably moved up into the overlying coal-measure sandstones along faults, prior to the Late Triassic. The high salinity and irregular salinity distribution in the Phalen sandstones suggests that the brines have undergone only modest dilution and are virtually immobile. In contrast, Prince waters show a progressive increase in salinity with depth and are inferred to have mixed with surface waters. Basinal brines from which these modern formation fluids were derived may have been important agents in base-metal and Ba mineralisation from the mid-Carboniferous onwards, as saline fluid inclusions are common in Zn–Pb sulphide deposits in the region.     

Formation of mineral and thermal waters of some artesian basins in Russia

Artesian basins contain the largest mineral water resources of the world. There are several types of mineral therapeutic water: sulfate, chloride, radon-rich, iron-rich waters, etc. Artesian basins occupy very large areas in Russia. However, genesis of water and brines is still not very clear. This is one of the most important hydrogeological problems that is being attempted to solve for many years. Most of the Russian hydrogeologists traditionally consider that these waters are of sedimentary origin. However, higher concentrations of bromine, iodine, iron, radon and other balneologically active components can be of different origin, for example, of infiltration or juvenile water. As an example, two areas will be considered – West-Siberian basin and East-European artesian area.West-Siberian artesian basin has very distinct latitudinal and vertical zonation. Latitudinal zonation is caused by climate changes from north to south. As for the vertical zonation, mineralization and chemical composition change in the vertical cross-section and from the periphery to the center within the same aquifer. The main mineral water resources of West-Siberian artesian basin are concentrated in Mesozoic rocks. Brackish waters and low-saturated brines without specific components are used for medical purposes. The most well-known spa is Karachi, which exploits chloride-hydrocarbonate brackish water. Sodium chloride bromine and iodine-bromine waters are used at other health resorts. It is possible to organize extraction of iodine from brines of Tcherkashinsko-Tobolskoe occurrence in Tumen region.East-European artesian area occupies most of the Russian Platform. The most widespread types of mineral water within the Russian Platform are sodium-chloride and magnesium-sulfate waters and brines. Such well-known spas, like Moscow mineral waters, Krainka, Staraya Russa and many others, belong to this type. Resources of these waters are definitely connected with sedimentogenic processes. The upper hydrodynamic zone contains iron-rich, hydrogen sulfide, and sometimes radon-rich water. Their formation is caused by the interaction between waters of infiltration and sedimentary genesis, or between infiltration waters and host rocks. One of the examples is Polustrovo iron-rich water. There are industrially valuable waters containing bromine and iodine.The resources of therapeutic water of sedimentary basins allow to increase balneological potential of spas in Russia.     

Origin of salinity in produced waters from the Palm Valley gas field,Northern Territory,Australia

The chemical composition and evolution of produced waters associated with gas production in the Palm Valley gas field, Northern Territory, has important implications for issues such as gas reserve calculations, reservoir management and saline water disposal. The occurrence of saline formation water in the Palm Valley field has been the subject of considerable debate. There were no occurrences of mobile water early in the development of the field and only after gas production had reduced the reservoir pressure, was saline formation water produced. Initially this was in small quantities but has increased dramatically with time, particularly after the initiation of compression in November 1996.The produced waters range from highly saline (up to 300,000 mg/L TDS), with unusual enrichments in Ca, Ba and Sr, to low salinity fluids that may represent condensate waters. The Sr isotopic compositions of the waters (⁸⁷Sr/⁸⁶Sr = 0.7041–0.7172) are also variable but do not correlate closely with major and trace element abundances. Although the extreme salinity suggests possible involvement of evaporite deposits lower in the stratigraphic sequence, the Sr isotopic composition of the high salinity waters suggests a more complex evolutionary history.The formation waters are chemically and isotopically heterogeneous and are not well mixed. The high salinity brines have Sr isotopic compositions and other geochemical characteristics more consistent with long-term residence within the reservoir rocks than with present-day derivation from a more distal pool of brines associated with evaporites. If the high salinity brines entered the reservoir during the Devonian uplift and were displaced by the reservoir gas into a stagnant pool, which has remained near the reservoir for the last 300–400 Ma, then the size of the brine pool is limited. At a minimum, it might be equivalent to the volume displaced by the reservoired gas.     

I and Cl in dilute hydrocarbon waters: Marine-cosmogenic, in situ, and anthropogenic sources

The long-lived halogen radioisotopes ¹²⁹I and ³⁶Cl provide valuable information regarding the source of fluids in hydrocarbon systems and in localized areas where infiltration of younger meteoric water has occurred. Despite the utility of these two isotopes in providing time-signatures for fluid end-members, considerable uncertainty remains regarding the interpretation of “intermediate-age” waters in hydrologic systems. These waters are likely the result of the combination of two or more halogen sources at some time in the past, each with its own characteristic concentration and isotopic composition. In order to unravel the evolution of these “intermediate-age” waters, the effect that infiltration of meteoric water has on the isotopic composition of older formation waters is modeled. Also evaluated is the effect that the timing of dilution has on ¹²⁹I and ³⁶Cl signatures observed in the present, specifically, the hypothesis that halogen isotopic signatures imparted by the mixing of brine and meteoric waters early in the development of a sedimentary basin are quantitatively different from those imparted by the mixing of old brines with recent meteoric waters.     

Br/Cl ratios and O, H, C, and B isotopic constraints on the origin of saline waters from eastern Canada

Saline groundwaters were recovered from undisturbed (Restigouche deposit) and active (Brunswick #12 mine) Zn-Pb volcanogenic massive sulfide deposits in the Bathurst Mining Camp (BMC), northern New Brunswick, Canada. These groundwaters, along with fresh to brackish meteoric ground and surface waters from the BMC, have been analyzed to determine their major, trace element and stable isotopic (O, H, C, and B) compositions. Saline groundwaters (total dissolved solids = 22-45 g/L) are characterized by relatively high Na/Ca ratios compared to brines from the Canadian Shield and low Na/Cl_molar and δ¹¹B isotopic compositions (−2.5‰ to 11.1‰) compared to seawater. Although saline waters from the Canadian Shield commonly have oxygen and hydrogen isotopic compositions that plot to the left of the global meteoric water line, those from the BMC fall close to the water line. Fracture and vein carbonate minerals at the Restigouche deposit have restricted carbon isotopic compositions of around −5‰ to −6‰. The carbon isotopic compositions of the saline waters at the Restigouche deposit (+12‰ δ¹³C_DIC) are the result of fractionation of dissolved inorganic carbon by methanogenesis. We suggest that, unlike previous models for shield brines, the composition of saline waters in the BMC is best explained by prolonged water-rock reaction, with no requirement of precursor seawater. We suggest that elevated Br/Cl ratios of saline waters compared to seawater may be explained by differential uptake of Br and Cl during groundwater evolution through water-rock reaction.     

Diagenetic and other highly mineralized waters in the Polish Carpathians

Highly mineralized waters of different chemical types and origin occur in the flysch formations and their bedrocks in the western part of the Polish Carpathians. The marine sedimentation water of the flysch formations is not preserved, as the most mineralized and the heaviest isotopic values of flysch waters are characterized by δ¹⁸O and δ²H values in the ranges of 5–7‰ and −(20–30)‰, respectively. Their origin is related to the dehydration of clay minerals during burial diagenesis, with molecules of marine water completely removed by molecules of released bound water. They are relatively enriched in Na⁺ in respect to the marine water, supposedly due to the release of Na⁺ during the illitization of smectites and preferable incorporation of other cations from the primary brine into newly formed minerals. In some parts of younger formations, i.e. in the Badenian sediments, brines occur with isotopic composition close to SMOW and Cl⁻ contents greatly exceeding the typical marine value of about 19.6 g/L, supposedly due to ultrafiltration. Most probably, the marine water of the flysch formations was similarly enriched chemically in its initial burial stages. Final Cl⁻ contents in diagenetic waters depend on different Cl⁻ contents in the primary brines and on relationships between diagenetic and further ultrafiltration processes. In some areas, diagenetic waters migrate to the surface along fault zones and mix with young local meteoric waters becoming diluted, with the isotope composition scattering along typical mixing lines. In areas with independent CO₂ flow from great depths, they form chloride CO₂-rich waters. Common CO₂-rich waters are formed in areas without near-surface occurrences of diagenetic waters. They change from the HCO₃–Ca type for modern waters to HCO₃–Mg–Ca, HCO₃–Na–Ca and other types with elevated TDS, Mg²⁺ and/or Na⁻ contents for old waters reaching even those of glacial age. Bedrocks of the flysch are represented by Mesozoic and Paleozoic mudstones, sandstones and carbonates, and in some areas by Badenian sediments. Brines of the Mesozoic and Paleozoic bedrocks are usually significantly enriched in Ca²⁺ and Mg²⁺ in comparison with the Badenian brines. By analogy to the deepest brines in the adjacent Upper Silesian Coal Basin, they are supposed to originate from paleometeoric waters of a hot climate.     

Origin and mixing history of brines,Palo Duro Basin,Texas, U.S.A.

Formation waters in the Palo Duro Basin, Texas, U.S.A. fall into four major groups based on integrated chemical and isotopic characteristics: (1) interbed brines within the major Permian evaporite aquitard; these are the most chemically concentrated and¹⁸O-rich fluids in the basin, and are interpreted as evaporatively concentrated sea water which has been hydrologically isolated since the Permian; (2) brines below the salt on the eastern side of the basin have ClBr, divalent cation, and isotopic systematics indicating a mixture of evaporatively concentrated sea water and meteoric water of δD= −20‰; (3) brines below the salt on the western side of the basin have chemical and isotopic systematics suggesting a mixture of two pulses of meteoric water, one with δD= −20‰ and the other with δD= −55‰; and (4) waters above the salt have the isotopic composition of meteoric waters. Diagenetic alteration of the cation chemistry has occurred for brines within and below the salt. Aquifers below the salt on the eastern side are interpreted as having been charged with dense Permian evaporite brines which subsequently mixed in various amounts with a basin-wide pulse of Triassic meteoric water. On the western side the descending Triassic meteoric waters became saline by dissolution of halite and are currently mixing with a Tertiary pulse of meteoric water initiated by the Laramide uplift to the west. The hydrochemistry suggests flow on the western side of the basin and static conditions on the eastern side. An unrecognized, approximately N-S permeability restriction, or discontinuity in the potentiometric flow surface, is inferred for major aquifers in the central area of the basin.     

The chemistry of bottled mineral and spring waters from Norway,Sweden, Finland and Iceland

Twenty-two bottled mineral and spring waters from Norway, Sweden, Finland and Iceland have been analysed for 71 inorganic chemical parameters with low detection limits as a subset of a large European survey of bottled groundwater chemistry (N = 884). The Nordic bottled groundwaters comprise mainly Ca–Na–HCO₃–Cl water types, but more distinct Ca–HCO₃, Na HCO₃ and Na–Cl water types are also offered. The distributions for most elements fall between groundwater from Fennoscandian Quaternary unconsolidated aquifers and groundwater from Norwegian crystalline bedrock boreholes. Treated tap waters have slightly lower median values for many parameters, but elements associated with plumbing have significantly higher concentrations in tap waters than in bottled waters. The small dataset is able to show that excessive fluoride and uranium contents are potential drinking water problems in Fennoscandia. Nitrate and arsenic displayed low to moderate concentrations, but the number of samples from Finland and Northern Sweden was too low to detect that elevated concentrations of arsenic occur in bedrock boreholes in some regions. The data shows clearly that water sold in plastic bottles is contaminated with antimony. Antimony is toxic and suspected to be carcinogenic, but the levels are well below the EU drinking water limit. The study does not provide any health-based arguments for buying bottled mineral and spring waters for those who are served with drinking water from public waterworks. Drinking water from crystalline bedrock aquifers should be analysed. In case of elevated concentrations of fluoride, uranium or arsenic, most bottled waters, but not all, will be better alternatives when treatment of the well water is not practicable.     

Identifying sources of salinization using hydrochemical and isotopic techniques, Konarsiah, Iran

Konarsiah salt diapir is situated in the Simply Folded Zone of the Zagros Mountain, south Iran. Eight small permanent brine springs emerge from the Konarsiah salt body, with average total dissolved solids of 326.7 g/L. There are numerous brackish to saline springs emerging from the alluvial and karst aquifers adjacent to the diapir. Concerning emergence of Konarsiah diapir in the study area, halite dissolution is the most probable source of salinity in the adjacent aquifers. However, other sources including evaporation and deep brines through deep Mangerak Fault are possible. The water samples of the study area were classified based on their water-type, salinity, and the trend of the ions concentration curves. The result of this classification is in agreement with the hydrogeological setting of the study area. The hydrochemical and isotopic evaluations show that the groundwater samples are the result of mixing of four end members; Gachsaran sulfate water, Sarvak and Asmari carbonate fresh waters, and diapir brine. The molar ratios of Na/Cl, Li/Cl, Br/Cl, and SO₄/Cl; and isotopic signature of the mixed samples justify a groundwater mixing model for the aquifers adjacent to the salt diapir. The share of brine in each adjacent aquifer was calculated using Cl mass balance. In addition, concentrations of 34 trace elements were determined to characterize the diapir brine and to identify the possible tracers of salinity sources in the mixed water samples. B, Mn, Rb, Sr, Cs, Tl, and Te were identified as trace elements evidencing contact of groundwater with the salt diapir.     

Cl-bearing lizardite in metamorphosed kimberlites from the Udachnaya Vostochnaya Pipe,Yakutia

Anhydrite-bearing dolomites and kimberlites from the contact zone of the Udachnaya Vostochnaya pipe, northern part of the Eastern Siberian Platform, were affected by low-grade metamorphism to the zeolite facies. The kimberlites are serpentinized and carbonatized and contain metasomes of anhydrite and saponite pockets. Twenty lizardite pseudomorphs after olivine (Fo _91–82) in the kimberlites were examined on an electron microprobe. The lizardite is rimmed by saponite and contains dolomite, calcite, magnetite, and anhydrite inclusions. Lizardite in the central parts of the pseudomorphs contains 1.5–1.9 wt % Cl and 6–9 wt % Fe₂O₃, and this mineral in the outer portions of the pseudomorphs bears 0.7–1.0 wt % Cl and 2–6 wt % Fe₂O₃ (the paper presents nine microprobe analyses and images showing the distribution of Cl, Mg, Al, Si, S, Ca, Ti, and Fe obtained in characteristic X-ray radiation). The amounts of Fe³⁺ in octahedrally and tetrahedrally coordinated sites of the Cl-bearing lizardite are roughly equal. Cl was borrowed in the course of serpentinization from the host Early Paleozoic evaporites and brines contained in them. The Cl concentration in our lizardite from the metamorphosed kimberlites from the Eastern Siberian Platform (continental lizardite) is much higher than the Cl concentration in oceanic lizardite from serpentine replacing peridotites (0.03–0.2 wt % Cl). This is likely explained by differences in the Cl concentrations in the metamorphic fluids, their salinity (3% for oceanic water and 65% for brines in the platform cover).     

Saline waters and residual brines in the Shiraz-Sarvistan basin,Iran

Origin of saline waters in the Shiraz-Sarvistan area, Iran, is determined by a combined isotopic (¹⁸O and D) and chemical characterization. Four types are recognized: (a) fresh water of the anticlinal carbonatic aquifer; (b) fresh and brackish runoff in the synclinal basins; (c) salt springs originating through dissolution of rock salt by type (a) fresh water; and (d) residual brines formed in synclinal closed drainage basins, through evaporation of former water types and loss of the relatively less-soluble salts.     

Isotope-geochemical systematics of kimberlites and related rocks from the Siberian Platform

Using the ICP-MS method we have studied the isotope systematics of Sr and Nd as well as trace element composition of a representative collection of kimberlites and related rocks from the Siberian Platform. The summarized literature and our own data suggest that the kimberlites developed within the platform can be divided into several petrochemical and geochemical types, whose origin is related to different mantle sources. The petrochemical classification of kimberlites is based on persistent differences of their composition in mg# and in contents of indicator oxides such as FeO_tot, TiO₂, and K₂O. The recognized geochemical types of kimberlites differ from one another in the level of concentration of incompatible elements as well as in their ratios.Most of isotope characteristics of kimberlites and related rocks of the Siberian Platform correspond to the earlier studied Type 1 basaltoid kimberlites from different provinces of the world: Points of isotopic compositions are in the field of primitive and weakly depleted mantle. An exception is one sample of the rocks from veins of the Ingashi field (Sayan area), which is characterized by the Sr and Nd isotopic composition corresponding to Type 2 micaceous kimberlites (orangeites).The most important feature of distribution of isotopic and trace-element compositions (incompatible elements) is their independence of the chemical rock composition. It is shown that the kimberlite formation is connected with, at least, two independent sources, fluid and melt, responsible for the trace-element and chemical compositions of the rock. It is supposed that, when rising through the heterogeneous lithosphere of the mantle, a powerful flow of an asthenosphere-derived fluid provoked the formation of local kimberlite chambers there. Thus, the partial melting of the lithosphere mantle led to the formation of contrasting petrochemical types of kimberlites, while the geochemical specialization of kimberlites is due to the mantle fluid of asthenosphere origin, which drastically dominated in the rare-metal balance of a hybrid magma of the chamber.     

Specifics of the late cenozoic geochemical evolution of chloride calcium brines in the Olenek cryoartesian basin

One of the probable mechanisms that controls the composition of highly mineralized chloride groundwaters is studied using physicochemical numerical simulations of equilibria in water–rock systems. Concentrated brines in the Olenek cryoartesian basin in the northeastern Siberian Platform are determined to be undersaturated with respect of major rock-forming minerals, which suggests that the metamorphosed sedimentary brines should have been diluted by meteoric waters during a certain evolutionary episode of the permafrost zone of the basin in the Late Pleistocene and Holocene.     

Geochemistry and origin of saline groundwaters in the Fennoscandian Shield

Chemical and isotopic analyses of water from drill holes and mines throughout the Fennoscandian Shield show that distinct layers of groundwater are present. An upper layer of fresh groundwater is underlain by several sharply differentiated saline layers, which may differ in salinity, relative abundance of solutes, and O, H, Sr and S isotope signature. Saline groundwater can be classified into four major groups based on geochemistry and presumed origin. Brackish and saline waters from 50–200 m depth in coastal areas around the Baltic Sea exhibit distinct marine chemical and isotopic fingerprints, modified by reactions with host rocks. These waters represent relict Holocene seawater. Inland, three types of saline groundwater are observed: an uppermost layer of brackish and saline water from 300–900 m depth; saline water and brines from 1000–2000 m depth; and superdeep brines which have been observed to a depth of at least 11 km in the drill hole on the Kola Peninsula, U.S.S.R. Electrical and seismic studies in shield areas suggest that such brines are commonly present at even greater depths. The salinity of all inland groundwaters is attributed predominantly to water-rock interaction. The main solutes are Cl, Ca, Na and Mg in varying proportions, depending on the host rock lithology. The abundance of dissolved gases increases with depth but varies from site to site. The main gas components are N₂, CH₄ (up to 87 vol.%) and locally H₂. The δ¹³C value for methane is highly variable (−25 to −46%), and it is suggested that hydrothermal or metamorphic gases trapped within the surrounding rocks are the most obvious source of CH₄. The uppermost saline water has meteoric oxygen-hydrogen isotopic compositions, whereas values from deeper water plot above the meteoric water line, indicating considerably longer mean residence time and effective low temperature equilibration with host rocks. Geochemical and isotopic results from some localities demonstrate that the upper saline water cannot have been formed through simple mixing between fresh water and deep brines but rather is of independent origin. The source of water itself has not been satisfactorily verified although superdeep brines at least may contain a significant proportion of relict Precambrian hydrothermal or metamorphic fluids.     

Hydrogeochemical and isotopic characteristics of the Ilica geothermal system (Erzurum,Turkey)

In this paper, the hydrochemical isotopic characteristics of samples collected from geothermal springs in the Ilica geothermal field, Eastern Anatolia of Turkey, are examined and described. Low-temperature geothermal system of Ilica (Erzurum, Turkey) located along the Eastern Anatolian fault zone was investigated for hydrogeochemical and isotopic characteristics. The study of ionic and isotopic contents shows that the thermal water of Ilica is mainly, locally fed by groundwater, which changes chemically and isotopically during its circulation within the major fault zone reaching depths. The thermal spring has a temperature of 29–39 °C, with electrical conductivity ranging from 4,000 to 7,510 µS/cm and the thermal water is of Na–HCO₃–Cl water type. The chemical geothermometers applied in the Ilica geothermal waters yielded a maximum reservoir temperature of 142 °C according to the silica geothermometers. The thermal waters are undersaturated with respect to gypsum, anhydrite and halite, and oversaturated with respect to dolomite. The dolomite mineral possibly caused scaling when obtaining the thermal waters in the study area. According to the enthalpy chloride-mixing model, cold water to the thermal water-mixing ratio is changing between 69.8 and 75 %. The δ¹⁸O–δ²H compositions obviously indicate meteoric origin of the waters. Thermal water springs derived from continental precipitation falling on to higher elevations in the study area. The δ¹³C ratio for dissolved inorganic carbonate in the waters lies between 4.63 and 6.48 ‰. In low-temperature waters carbon is considered as originating from volcanic (mantle) CO₂.