Geochemistry of geopressured hydrothermal waters in the Niigata Sedimentary Basin, Japan

Abstract   Geothermal waters in the Niigata Sedimentary Basin, central Japan, are divided into four groups based on their chemical composition (i.e. Na-SO₄-type, Na-SO₄-Cl-type, Na-Cl-type and Na-Cl-HCO₃-type). The Na-SO₄-type geothermal water forms as a consequence of water–rock interaction and generally occurs in the outer part of the basin. The Na-Cl-type geothermal water is further subdivided into the original Na-Cl-type geopressured thermal water and the mixed Na-Cl-type geothermal water, in terms of its geochemical and isotopic composition. The original Na-Cl-type geopressured thermal water originates from a geopressured hydrothermal system containing the altered fossil formation waters that are sealed at depth. It moves up to the upper part of the depositional succession or the ground, and generally does not mix with groundwater that is of meteoric origin. This type of water is cooled by heat conduction. The concentration of Cl^– in this type of thermal water is very similar to that in seawater. The δD and δ¹⁸O values are approximately constant and independent of temperature. The original Na-Cl-type geopressured thermal water is distributed mainly along anticlinal axes in folded Neogene formations. The mixed Na-Cl-type geothermal water is related to the expulsion activity of the geopressured hydrothermal system and occurs mostly along active faults. It is formed by shallow groundwater of meteoric origin being mixed with geopressured hydrothermal water when the geopressured hydrothermal system was expulsed along active faults by paroxysmal tectonic events.     

The hydrothermal system of Mendeleev Volcano,Kunashir Island,Kuril Islands: The geochemistry and the transport of magmatic components

This paper reports a detailed geochemical study of thermal occurrences as observed in the edifice and on the flanks of Mendeleev Volcano, Kunashir Island in August and September 2015. We showed that three main types of thermal water are discharged there (neutral chloride sodium, acid chloride sulfate, and acid sulfate types); these waters exhibit a zonality that is typical of volcano-hydrothermal island arc systems. Spontaneous and solfataric gases have relatively low ³He/⁴He ratios, ranging between 5.4Ra and 5.6Ra, and δ¹³C-CO₂ between –4.8‰ and –3.1‰, and contain a light isotope of carbon in methane (δ¹³C ≈ –40‰). Gas and isotope geothermometers yield relatively low temperatures around 200°C. The isotope compositions in all types of water are similar to that of local meteoric water. The distribution of microcomponents varies among different types. The isotope composition of dissolved Sr varies considerably, from 0.7034 as observed in Kunashir rocks on an average to 0.7052 in coastal springs, which may have resulted from admixtures of seawater. The total hydrothermal transport rates of magmatic Cl and SO₄, as observed for Mendeleev Volcano, are 7.8 t/d and 11.6 t/d, respectively. The natural outward transport of heat by the volcano’s hydrothermal system is estimated as 21 MW.     

Geochemistry of waters in the Valley of Ten Thousand Smokes region, Alaska

Meteoric waters from cold springs and streams outside of the 1912 eruptive deposits filling the Valley of Ten Thousand Smokes (VTTS) and in the upper parts of the two major rivers draining the 1912 deposits have similar chemical trends. Thermal springs issue in the mid-valley area along a 300-m lateral section of ash-flow tuff, and range in temperature from 21 to 29.8°C in early summer and from 15 to 17°C in mid-summer. Concentrations of major and minor chemical constituents in the thermal waters are nearly identical regardless of temperature. Waters in the downvalley parts of the rivers draining the 1912 deposits are mainly mixtures of cold meteoric waters and thermal waters of which the mid-valley thermal spring waters are representative. The weathering reactions of cold waters with the 1912 deposits appear to have stabilized and add only subordinate amounts of chemical constituents to the rivers relative to those contributed by the thermal waters. Isotopic data indicate that the mid-valley thermal spring waters are meteoric, but data is inconclusive regarding the heat source. The thermal waters could be either from a shallow part of a hydrothermal system beneath the 1912 vent region or from an incompletely cooled, welded tuff lens deep in the 1912 ash-flow sheet of the upper River Lethe area.Bicarbonate-sulfate waters resulting from interaction of near-surface waters and the cooling 1953–1968 southwest Trident plug issue from thermal springs south of Katmai Pass and near Mageik Creek, although the Mageik Creek spring waters are from a well-established, more deeply circulating hydrothermal system. Katmai caldera lake waters are a result of acid gases from vigorous drowned fumaroles dissolving in lake waters composed of snowmelt and precipitation.     

Isotopic geochemistry of acid thermal waters and volcanic gases from Zaō volcano in Japan

The chemical composition and D/H, and ratios have been determined for the acid hot waters and volcanic gases discharging from Zaō volcano in Japan. The thermal springs in Zaō volcano issue acid sulfate-chloride type waters (Zaō) and acid sulfate type waters (Kamoshika). Gases emitted at Kamoshika fumaroles are rich in CO₂, SO₂ and N₂, exclusive of H₂O. Chloride concentrations and oxygen isotope data indicate that the Zaō thermal waters issue a fluid mixture from an acid thermal reservoir and meteoric waters from shallow aquifers. The waters in the Zaō volcanic system have slight isotopic shifts from the respective local meteoric values. The isotopic evidence indicates that most of the water in the system is meteoric in origin. Sulfates in Zaō acid sulfate-chloride waters with δ³⁴S values of around +15‰, are enriched in ³⁴S compared to Zaō H₂S, while the acid sulfate waters at Kamoshika contain supergene light sulfate (δ³⁴S = + 4‰) derived from volcanic sulfur dioxide from the volcanic exhalations. The sulfur species in Zaō acid waters are lighter in δ³⁴S than those of other volcanic areas, reflecting the difference in total pressure.     

Hydrogen and oxygen isotope ratios in the waters of the Ngawha hydrothermal area,North Auckland

The ratios of D/H and O¹⁸/O¹⁶ in natural waters from streams, boreholes, soda springs, hot pools, ponds and larger bodies of water in the Ngawha hydrothermal area were determined. The results are considered in relation to the isotopic changes known to occur in water subjected to evaporation. Where applicable chemical and other work was also considered. It is assumed that stream water isotope composition is the mean value for the isotopic composition of meteoric waters. Measurements on waters taken from boreholes drilled to 65 feet and 350 feet and from the other water sources mentioned, indicate that they were of meteoric origin as judged by stream isotope composition. The waters from the soda springs appeared to be isotopically the same as the stream water, a finding consistent with the absence of evaporative surface. These borehole waters were similar but slightly different in O¹⁸ due probably to exchange between rock and water. Heavy isotope enrichment of the ponds and larger bodies of water appeared to be due to non-equilibrium evaporation at ambient temperature. The hot pools in the Ngawha springs area proper were enriched in the heavier isotopes probably due to non-equilibrium evaporation at the usual hot pool temperature of about 40°C and also to exchange of O¹⁸ between water and rock. The water from a further borehole drilled to approximately 2,000 feet appeared also to be of meteoric origin but was changed in O¹⁸ content to an extent consistent with the assumption that oxygen isotope exchange with rock had taken place at approximately 230°C. The results are used to illustrate possibilities for the use of oxygen and hydrogen isotope measurements in hydrothermal investigations.     

Chemical and isotopic signatures of the basement rocks from the Campi Flegrei geothermal field (Naples, southern Italy): inferences about the origin and evolution of its hydrothermal fluids

The Campi Flegrei (Naples, Campanian Plain, southern Italy) geothermal system is hosted by Quaternary volcanic rocks erupted before, during and after the formation of the caldera that represents one of the major structural features in the Neapolitan area. The volcanic products rest on a Mesozoic carbonate basement, cropping out north, east and south of the area. Chemical (major, minor and trace elements) and stable isotope (C, H, O) analyses were conducted on drill-core samples recovered from geothermal wells MF-1, MF-5, SV-1 and SV-3, at depths of ˜ 1100 to 2900 m. The study was complemented by petrographic and SEM examination of thin sections. The water which feeds the system is both marine and meteoric in origin. Mineral zonation typical of a high-temperature geothermal system exists in all the geothermal wells; measured temperatures in wells are as high as ˜ 400 °C. The chemical composition of the waters suggests the existence of two reservoirs: a shallow reservoir (depth < 2000 m) fed by seawater that boiled at 320 °C and became progressively diluted by steam-heated local meteoric water during its ascent; and a deeper reservoir (depth > 2000 m) of hypersaline water. The drill-cores are mainly hydrothermally altered volcanics of trachy-latitic affinity, but some altered pelites and limestones are also present. Published Na, Mg and K concentrations of selected geothermal waters indicate that the hydrothermal fluids are in equilibrium with their host rocks, with respect to K-feldspar, albite, sericite and chlorite. The measured δ¹⁸O_(SMOW) values of rocks range from +4.3 to + 16.5%. The measured δD_(SMOW) values range from − 79 to − 46%. The calculated isotopic composition of the fluids at equilibrium with the samples vary from + 1 to + 8.3%. δ¹⁸O and from − 52 to + 1%. δD. The estimated isotopic composition of the waters at equilibrium with the studied samples confirmed the existence of two distinct fluid types circulating in the geothermal system. The shallower has a marine water signature, while the deeper water has a signature consistent both with magmatic and meteoric origins. In the latter case, the recharge of this aquifer likely occurs at the outcrop of the Mesozoic Limestones surrounding the Campanian Plain; after infiltration, the water percolates through evaporitic layers, becoming hypersaline and D-depleted.     

Mineralogy and hydrogen isotope geochemistry of clay minerals in the Ohnuma geothermal area,Northeastern Japan

Mineralogical and hydrogen isotopic studies have been made on clay minerals occurring in the Ohnuma geothermal area, northeastern Japan. Here, clay minerals such as smectite, kaolinite, dickite, sericite, and chlorite were formed by hydrothermal alteration of Miocene rocks. A chemical equilibrium can be assumed to be attained from the fact that the amount of expandable layer in the interstratified chlorite/smectite decreases and the polytype of sericite changes from 1M to 2M₁ with increasing depth and temperature. The hydrogen isotopic composition (D/H) of the clay minerals is lighter than that of the geothermal and local meteoric waters by about 20–40‰. The hydrogen isotopic fractionation factors α_{mineral-water} are as follows: 0.972–0.985 for kaolinite and dickite, 0.973–0.977 for sericite, and 0.954–0.987 for chlorite. In the temperature range from 100 to 250°C, the hydrogen isotopic fractionation factors between these minerals and water are not sensitive to the temperature. α_{chlorite-water} depends on the kind of octahedrally coordinated cations which lie close to the hydroxyl groups; it becomes large with an increase of Mg content of chlorite.     

Volcanic lake systematics II. Chemical constraints

A database of 373 lake water analyses from the published literature was compiled and used to explore the geochemical systematics of volcanic lakes. Binary correlations and principal component analysis indicate strong internal coherence among most chemical parameters. Compositional variations are influenced by the flux of magmatic volatiles and/or deep hydrothermal fluids. The chemistry of the fluid entering a lake may be dominated by a high-temperature volcanic gas component or by a lower-temperature fluid that has interacted extensively with volcanic rocks. Precipitation of minerals like gypsum and silica can strongly affect the concentrations of Ca and Si in some lakes. A much less concentrated geothermal input fluid provides the mineralized components of some more dilute lakes. Temporal variations in dilution and evaporation rates ultimately control absolute concentrations of dissolved constituents, but not conservative element ratios.Most volcanic lake waters, and presumably their deep hydrothermal fluid inputs, classify as immature acid fluids that have not equilibrated with common secondary silicates such as clays or zeolites. Many such fluids may have equilibrated with secondary minerals earlier in their history but were re-acidified by mixing with fresh volcanic fluids. We use the concept of ‘degree of neutralization’ as a new parameter to characterize these acid fluids. This leads to a classification of gas-dominated versus rock-dominated lake waters. A further classification is based on a cluster analysis and a hydrothermal speedometer concept which uses the degree of silica equilibration of a fluid during cooling and dilution to evaluate the rate of fluid equilibration in volcano-hydrothermal systems.     

Geochemical Monitoring of Geothermal Waters (2002–2004) along the North Anatolian Fault Zone, Turkey: Spatial and Temporal Variations and Relationship to Seismic Activity

A total of nine geothermal fields located along an 800-km long E-W transect of the North Anatolian Fault Zone (NAFZ), Turkey were monitored for three years (2002–2004 inclusive; 3-sampling periods per year) to investigate any possible relationship between seismic activity and temporal variations in the chemistry and isotope characteristics of waters in the fields. The geothermal fields monitored in the study were, from west to east, Yalova, Efteni, Bolu, Mudurnu, Seben, Kur?unlu-Çank?r?, Hamamözü, Gözlek and Re?adiye. The chemical (major anion-cation contents) and isotopic (¹⁸O/¹⁶O, D/H, ³H) compositions of hot and cold waters of the geothermal sites were determined in order to both characterize the chemical nature of the individual fields and identify possible temporal variations associated with localized seismic activity. The geothermal waters associated with the NAFZ are dominantly Na-HCO₃, whereas the cold waters are of the Ca-HCO₃ type. The oxygen- and hydrogen-isotope compositions reveal that the hot waters are meteoric in origin as are their cold water counterparts. However, the lower δ¹⁸O, δD and ³H contents of the hot waters point to the fact that they are older than the cold waters, and that their host aquifers are recharged from higher altitudes with virtually no input from recent (post-bomb) precipitation. Although no major earthquakes (e.g., with M ≥ 5) were recorded along the NAFZ during the course of the monitoring period, variations in the chemical and isotopic compositions of some waters were observed. Indeed, the timing of the chemical/isotopic changes seems to correlate with the occurrence of seismic activity of moderate magnitude (3 < M < 5) close to the sampling sites. In this respect, Cl, ³H and Ca seem to be the most sensitive tracers of seismically-induced crustal perturbations, and the Yalova and Efteni fields appear to be the key localities where the effects of seismic activity on the geothermal fluids are most pronounced over the monitoring period. The present study has produced a ‘baseline’ database for future studies directed at characterizing the effects of moderate-major earthquakes on the composition of geothermal waters along the NAFZ. Future work involving longer monitoring periods with more frequent sampling intervals should lead to a better understanding of the underlying mechanism(s) producing the observed chemical and isotopic variations.     

The chemical and hydrologic structure of Poa´s Volcano, Costa Rica

Comparison of the chemical characteristics of spring and river water draining the flanks of Poa´s Volcano, Costa Rica indicates that acid chloride sulfate springs of the northwestern flank of the volcano are derived by leakage and mixing of acid brines formed in the summit hydrothermal system with dilute flank groundwater. Acid chloride sulfate waters of the Rio Agrio drainage basin on the northwestern flank are the only waters on Poa´s that are affected by leakage of acid brines from the summit hydrothermal system. Acid sulfate waters found on the northwestern flank are produced by the interaction of surface and shallow groundwater with dry and wet acid deposition of SO₂ and H₂SO₄ aerosols, respectively. The acid deposition is caused by a plume of acid gases that is released by a shallow magma body located beneath the active crater of Poa´s.No evidence for a deep reservoir of neutral pH sodium chloride brine is found at Poa´s. The lack of discharge of sodium chloride waters at Poa´s is attributed to two factors: (1) the presence of a relatively volatile-rich magma body degassing at shallow depths (< 1 km) into a high level summit groundwater system; and (2) the hydrologic structure of the volcano in which high rates of recharge combine with rapid lateral flow of shallow groundwater to prevent deep-seated sodium chloride fluids from ascending to the surface. The shallow depth of the volatile-rich magma results in the degassing of large quantities of SO₂ and HCl. These gases are readily hydrolyzed and quickly mix with meteoric water to form a reservoir of acid chloride-sulfate brine in the summit hydrothermal system. High recharge rates and steep hydraulic gradients associated with elevated topographic features of the summit region promote lateral flow of acid brines generated in the summit hydrothermal system. However, the same high recharge rates and steep hydraulic gradients prevent lateral flow of deep-seated fluids, thereby masking the presence of any sodium chloride brines that may exist in deeper parts of the volcanic edifice.Structural, stratigraphic, and topographic features of Poa´s Volcano are critical in restricting flow of acid brines to the northwestern flank of the volcano. A permeable lava-lahar sequence that outcrops in the Rio Agrio drainage basin forms a hydraulic conduit between the crater lake and acid chloride sulfate springs. Spring water residence times are estimated from tritium data and indicate that flow of acid brines from the active crater to the Rio Agrio source springs is relatively rapid (3 to 17 years). Hydraulic conductivity values of the lava-lahar sequence calculated from residence time estimates range from 10⁻⁵ to 10⁻⁷ m/s. These values are consistent with hydraulic conductivity values determined by aquifer tests of fractured and porous lava/pyroclastic sequences at the base of the northwestern flank of the volcano.Fluxes of dissolved rock-forming elements in Rio Agrio indicate that approximately 4300 and 1650 m³ of rock are removed annually from the northwest flank aquifer and the active crater hydrothermal system, respectively. Over the lifetime of the hydrothermal system (100's to 1000's of years), significant increases in aquifer porosity and permeability should occur, in marked contrast to the reduction in permeability that often accompanies hydrothermal alteration in less acidic systems. Average fluxes of fluoride, chloride and sulfur calculated from discharge and compositional data collected in the Rio Agrio drainage basin over the period 1988–1990 are approximately 2, 38 and 30 metric tons/day. These fluxes should be representative of minimum volatile release rates at Poa´s in the last 10 to 20 years.     

Chemical and stable isotopic models for boundary creek warm springs, southwestern Yellowstone National Park, Wyoming

Thermal springs of the Boundary Creek hydrothermal system in the southwestern part of Yellowstone Park outside the caldera boundary vary in chemical and isotopic composition, and temperature. The diversity may be accounted for by a combination of processes including boiling of a deep thermal water, mixing of the deep thermal water with cool meteoric water and/or with condensed steam or steam-heated meteoric water, and chemical reactions with surrounding rocks. Dissolved-silica, Na⁺, K⁺ and Ca²⁺ contents of the thermal springs could result from a thermal fluid with a temperature of 200 ± 20°C. Chloride-enthalpy and silica-enthalpy mixing models suggest mixing of 230°C, 220 mg/l Cl⁻ thermal water with cool, low-Cl⁻ components. A 350 to 390°C component with Cl⁻ ≥ 300 mg/l is possibly present in thermal springs inside the caldera but is not required to fit observed spring chemical and isotopic compositions. Irreversible mass transfer models in which a low-temperature water reacts with volcanic glass as it percolates downward and warms, can account for observed pH and dissolved-silica, K⁺, Na⁺, Ca²⁺ and Mg²⁺ concentrations, but produces insufficient Cl⁻ or F⁻ for measured concentrations in the warm springs. The ratio of a_Na/a_H, and Cl⁻ are best accounted for in mixing models. The water-rock interaction model fits compositions of acid-sulfate waters observed at Summit Lake and of low-Cl⁻ waters involved in mixing.The cold waters collected from southwestern Yellowstone Park have δD values ranging from −118 to −145 per mil and δ¹⁸O values of −15.9 to −19.4 per mil. Two samples from nearby Island Park have δD values of −112 and −114 per mil and δ¹⁸O values of −15.1 and −15.3 per mil. All samples of thermal water plot significantly to the right of the meteoric water line. The low Cl⁻ and variable δD values of the thermal waters indicate isotopic compositions are derived by extensive dilution with cold meteoric water and by steam separation on ascent to the surface. Many of the hot springs with higher δD values may contain in addition a significant amount of high-D, low-Cl⁻, acid-sulfate or steam-heated meteoric water. Mixing models, Cl⁻ content and isotopic compositions of thermal springs suggest that 30% or less of a deep thermal component is present. For example, the highest-temperature springs from Three Rivers, Silver Scarf and Upper Boundary Creek thermal areas contain up to 70% cool meteoric water and 30% hot water components, springs at Summit Lake and Middle Boundary Creek spring 57 are acid-sulfate or steam-heated meteoric water; springs 27 and 48 from Middle Boundary Creek and 49 from Mountain Ash contain in excess of 50% acid-sulfate water; and Three Rivers spring 46 and Phillips could result from mixing hot water with 55% cool meteoric water followed by mixing of acid-sulfate water. Extensive dilution by cool meteoric water increases the uncertainties in quantity and nature of the deep meteoric, thermal component.     

Hydrogeochemical outline of thermal waters and geothermometry applications in Anatolia (Turkey)

The chemical compositions of a total of 120 thermal water samples from four different tectonically distinct regions (Central, North, East and West Anatolia) of Turkey are presented and assessed in terms of geothermal energy potential of each region through the use of chemical geothermometers. Na–Ca–HCO₃ type waters are the dominant water types in all the regions except that Na–Cl type waters are typical for the coastal areas of West Anatolia and for a few inland areas of West and Central Anatolia where deep water circulation exists. The discharge temperature of the springs ranges up to 100°C, and the bottom-hole temperatures in drilled wells up to 232°C. Geothermometry applications yield reservoir temperatures of about 125°C for Central Anatolia, 110°C for North Anatolia, 136°C for East Anatolia and 251°C for West Anatolia, the latter agreeing with some of the bottom hole temperatures measured in drilled wells. The results reveal that the highest geothermal energy potential in Turkey is associated with the West Anatolian extensional tectonics which provides a regional, deep-seated heat source and a widespread graben system allowing deep circulation of waters. The North Anatolian region, bounded to the south by the dextral North Anatolian Fault along which most of the geothermal sites are located, has the lowest energy potential, probably due to the restriction of the heat source to local magmatic activities confined to pull-apart basins. The East Anatolian region (undergoing contemporary compression) and the Central Anatolian region (where the compressional regime in the east is converted to the extensional regime in the west) have moderate energy potential. Although the recently active volcanoes suggest the presence, at depth, of still cooling magma chambers that are potential heat sources, the lack of well-developed fault systems is probably responsible for the comparatively low energy potential of these regions. Almost all the thermal waters of Turkey are saturated with respect to calcite and, hence, have a significant calcite scaling potential which is particularly high for West Anatolian waters.     

Chemical and isotopic changes in the hydrology of the tauhara geothermal field due to exploitation at wairakei

Depressurisation of the Tauhara field due to massive withdrawal of deep chloride water from the adjacent Wairakei field for geothermal power has caused considerably hydrological and chemical changes at Tauhara. In the undisturbed state (1962), deep chloride water discharged as hot and boiling dilute chloride springs on the east and west flanks of the field (the Terrace and Spa areas, respectively), while steam from the two-phase zone of the deep system produced by absorption into near-surface groundwater, steam-heated sulphatebicarbonate waters and by mixing with chloride water, chloride-sulphate waters. By 1978–1981 the chloride waters had stopped discharging on the western flank, the steam flow towards the surface had greatly increased (by 5–10 fold) increasing the volume and temperature of the steam-heated waters, but the dilute chloride waters of the Terrace area had changed very little. Silica concentrations in the near-surface waters appear to be controlled by the solubility of amorphous silica, which is present in the surface zone rocks (e.g., Taupo pumice breccias). The increased steam flow led to enrichment in the ¹³O and D contents of the steam-heated waters by loss of secondary steam and enlargement of the area and intensity of steaming ground, the latter accompanied by hydrothermal eruptions in 1974 and 1981. Generation of the steam-heated waters has been modelled using mass, heat and isotope balances. The model is consistent with observed heat and cold groundwater flows and requires that a large proportion of the heat from adsorbed primary steam is released as secondary steam. Tritium contents show that the steam-heated waters have a mean residence time of 50–100 years. In the future, invasion of the deep system by cooler surface waters may reduce steam flow and lower surface aquifer temperatures.     

Chemical composition of thermal springs, cold springs, streams, and gas vents in the Mt. Amiata geothermal region (Tuscany, Italy)

A geochemical study of thermal and cold springs, stream waters and gas emissions has been carried out in the Mt. Amiata geothermal region.The cold springs and stream waters do not seem to have received significant contribution from hot deep fluids. On the contrary, the thermal springs present complex and not clearly quantifiable interactions with the hot fluids of the main geothermal reservoir.The liquid-dominated systems in the Mt. Amiata area, like most of the high-enthalpy geothermal fields in the world, are characterized by saline, NaCl fluids. The nature of the reservoir rock (carbonatic and anhydritic), and its widespread occurrence in central Italy, favor a regional circulation of “Ca-sulfate” thermal waters, which discharge from its outcrop areas. Waters of this kind, which have been considered recharge waters of the known geothermal fields, dilute, disperse and react with the deep geothermal fluids in the Mt. Amiata area, preventing the use of the main chemical geothermometers for prospecting purposes. The temperatures obtained from the chemical geothermometers vary widely and are generally cooler than temperatures measured in producing wells.Other thermal anomalies in central Italy, apart from those already known, might be masked by the above-mentioned circulation. A better knowledge of deep-fluid chemistry could contribute to the calibration of specific geothermometers for waters from reservoirs in carbonatic rocks.     

Hot springs of Rhodesia: Their noble gases,isotopic and chemical composition

Four of Rhodesia's hottest spring complexes (54–100°C) were studied. Tritium contents were very low, compared to adjacent rivers, indicating that the samples studied were indigenous, deep-seated water which had undergone negligible intermixing with surface water.The noble-gas measurements revealed: (1) the waters are meteoric; (2) the noble gases were kept in closed-system conditions in the ground; (3) paleotemperatures are 26–31°C; (4) the boiling Binga springs lost part of their noble gases.Independently, measurements of stable isotopes indicate the meteoric origin of the springs. The chemical composition of the waters clearly reflects their origin from two groups of rocks — one from Karroo sediments and one from crystalline rocks.     

Spatial and temporal changes in microbial diversity of the Marmara Sea sediments

Spatial (10 different locations) and temporal (2 years) changes in characteristics of the Marmara Sea Sediments were monitored to determine interactions between the chemical and microbial diversity. The sediments were rich in terms of hydrocarbon, nitrate, Ni and microbial cell content. Denitrifying, sulfate reducing, fermentative and methanogenic organisms were co-abundant in 15 cm below the sea floor. The local variations in the sediments’ characteristics were more distinctive than the temporal ones. The sulfate and nitrate contents were the main drivers of the changes in the microbial community compositions. N and P were limited for microbial growth in the sediments, and their levels determined the total cell abundance and activity. Seasonal shifts in temperatures of the shallow sediments were also reflected in the active cell abundances. It was concluded that the Marmara Sea is a promising ecosystem for the further investigation of the ecologically important microbial processes.     

INTEGRATED EXPLORATION FOR LOW-TEMPERATURE GEOTHERMAL RESOURCES IN THE HONEY LAKE BASIN,CALIFORNIA1

An integrated exploration study is presented to locate low-temperature geothermal reservoirs in the Honey Lake area of northern California. Regional studies to locate the geothermal resources included gravity, infra-red, water-temperature, and water-quality analyses. Five anomalies were mapped from resistivity surveys. Additional study of three anomalies by temperature-gradient and seismic methods was undertaken to define structure and potential of the geothermal resource. The gravity data show a graben structure in the area. Seismic reflection data indicate faults associated with surface-resistivity and temperature-gradient data. The data support the interpretation that the shallow reservoirs are replenished along the fault zones by deeply circulating heated meteoric waters.     

“Andesitic water”: a phantom of the isotopic evolution of water-silicate systems. Comment on “Isotopic shifts in waters from geothermal and volcanic systems along convergent plate boundaries and their origin” by W.F. Giggenbach

On account of the low porosity of the lithosphere, intracrustal fluids behave very differently from surface fluids, in that they are changing their geochemical and isotopic labels according to the geological environment. Given a heat source, meteoric waters can be supplied plentifully and their rates of throughput in geothermal systems are sufficiently high to exhaust the compositional signals of a given rock buffer. In contrast, fluids exsolved from magma, and subducted fluids, would be supplied at less than about one tenth of the meteoric rate over the life time of a system. Based on up-to-date flow models, the isotopic evolution of meteoric water interacting with crustal rock follows a curved to L-shaped track in the δD versus δ¹⁸O plot. Instantaneous (present-day) tie-lines between recharge and discharge are secants of such tracks and can have a range of slopes. At the start of an interaction, waters have δD and δ¹⁸O values approaching equilibrium with the original rock composition (water “W1”). Using known hydrogen isotope fractionation factors, W1 values generally plot in the region of “andesite” or “andesitic” waters of various authors. Since the W1 waters have δD values that are on average more positive, and also less variable than those of the meteoric recharges, most tracks and tie-lines have positive slopes, and the plotting of a large number of tie-lines will produce a focus on the field of W1 waters, regardless of the original water source.     

Fluid geochemistry of natural manifestations from the Southern Poroto–Rungwe hydrothermal system (Tanzania): Preliminary conceptual model

The South Poroto–Rungwe geothermal field, in the northern part of the Malawi rift, Tanzania divides in two main areas. The relatively high altitude northern area around the main Ngozi, Rungwe, Tukuyu and Kyejo volcanoes, is characterised by cold and gas-rich springs. In contrast, hot springs occur in the southern and low-altitude area between the Kyela and Livingstone faults. The isotopic signature of the almost stagnant, cold springs of the Northern district is clearly influenced by H₂O–CO_2(g) exchange as evidenced from negative oxygen-shifts in the order of few deltas permil. In contrast, the isotopic signature of waters discharged from the hot springs of the Southern district is markedly less affected by the H₂O–CO_2(g) interaction. This evidence is interpreted as an effect of the large, permanent outflow of these springs, which supports the hypothesis of a regional-scale recharge of the major thermal springs. Measurements of carbon isotope variations of the dissolved inorganic carbon of waters and CO_2(g) from the Northern and Southern springs support a model of CO_2(g)-driven reactivity all over the investigated area. Our combined chemical and isotopic results show that the composition of hot springs is consistent with a mixing between (i) cold surface fresh (SFW) and (ii) Deep Hot Mineralised (DHMW) Water, indicating that the deep-originated fluids also supply most of the aqueous species dissolved in the surface waters used as local potable water. Based on geothermometric approaches, the temperature of the deep hydrothermal system has been estimated to be higher than 110 °C up to 185 °C, in agreement with the geological and thermal setting of the Malawi rift basin. Geochemical data point to (i) a major upflow zone of geothermal fluids mixed with shallow meteoric waters in the Southern part of the province, and (ii) gas absorption phenomena in the small, perched aquifers of the Northern volcanic highlands.