Geothermal Reservoir Temperatures in Southeastern Idaho using Multicomponent Geothermometry

Energy Technology Data Exchange (ETDEWEB)

Neupane, Ghanashyam [Idaho National Lab. (INL) and Center for Advanced Energy Studies, Idaho Falls, ID (United States); Mattson, Earl D. [Idaho National Lab. (INL) and Center for Advanced Energy Studies, Idaho Falls, ID (United States); McLing, Travis L. [Idaho National Lab. (INL), Idaho Falls, ID (United States). Center for Advanced Energy Studies; Palmer, Carl D. [Univ. of Idaho, Idaho Falls, ID (United States); Smith, Robert W. [Univ. of Idaho and Center for Advanced Energy Studies, Idaho Falls, ID (United States); Wood, Thomas R. [Univ. of Idaho and Center for Advanced Energy Studies, Idaho Falls, ID (United States); Podgorney, Robert K. [Idaho National Lab. (INL) and Center for Advanced Energy Studies, Idaho Falls, ID (United States)

2015-03-01

Southeastern Idaho exhibits numerous warm springs, warm water from shallow wells, and hot water within oil and gas test wells that indicate a potential for geothermal development in the area. Although the area exhibits several thermal expressions, the measured geothermal gradients vary substantially (19 – 61 ºC/km) within this area, potentially suggesting a redistribution of heat in the overlying ground water from deeper geothermal reservoirs. We have estimated reservoir temperatures from measured water compositions using an inverse modeling technique (Reservoir Temperature Estimator, RTEst) that calculates the temperature at which multiple minerals are simultaneously at equilibrium while explicitly accounting for the possible loss of volatile constituents (e.g., CO2), boiling and/or water mixing. Compositions of a selected group of thermal waters representing southeastern Idaho hot/warm springs and wells were used for the development of temperature estimates. The temperature estimates in the the region varied from moderately warm (59 ºC) to over 175 ºC. Specifically, hot springs near Preston, Idaho resulted in the highest temperature estimates in the region.

Geothermal Reservoir Temperatures in Southeastern Idaho using Multicomponent Geothermometry

International Nuclear Information System (INIS)

Neupane, Ghanashyam; Mattson, Earl D.; McLing, Travis L.; Smith, Robert W.; Wood, Thomas R.; Podgorney, Robert K.

2015-01-01

Southeastern Idaho exhibits numerous warm springs, warm water from shallow wells, and hot water within oil and gas test wells that indicate a potential for geothermal development in the area. Although the area exhibits several thermal expressions, the measured geothermal gradients vary substantially (19 - 61 °C/km) within this area, potentially suggesting a redistribution of heat in the overlying ground water from deeper geothermal reservoirs. We have estimated reservoir temperatures from measured water compositions using an inverse modeling technique (Reservoir Temperature Estimator, RTEst) that calculates the temperature at which multiple minerals are simultaneously at equilibrium while explicitly accounting for the possible loss of volatile constituents (e.g., CO2), boiling and/or water mixing. Compositions of a selected group of thermal waters representing southeastern Idaho hot/warm springs and wells were used for the development of temperature estimates. The temperature estimates in the the region varied from moderately warm (59 °C) to over 175 °C. Specifically, hot springs near Preston, Idaho resulted in the highest temperature estimates in the region.

Intracrystalline "geothermometry" assessed on clino and orthopyroxene bearing synthetic rocks

Science.gov (United States)

Murri, M.; Cámara, F.; Adam, J.; Domeneghetti, M. C.; Alvaro, M.

2018-04-01

Recent discussion on the application of intracrystalline "geothermometers" based on the Fe-Mg order-disorder reaction in pyroxene in natural rocks, indicates that the available calibration equations for clino and orthopyroxenes (cpx and opx), which express the equilibrium intracrystalline Fe-Mg distribution coefficient kD(Fe-Mg) as a function of temperature, require independent validation. In this paper, we tested the available experimental calibrations for clino and orthopyroxenes by determining the site occupancies of these minerals in synthetic samples grown from a hydrous nepheline basanite in a piston-cylinder apparatus at 1050 °C at 2.0 GPa to 1170 °C at 3.0 GPa, and quenched very rapidly by shutting off the power. The site occupancies were determined by single crystal X-ray diffraction (SC-XRD) and used to calculate the closure temperature, TC, of cation ordering using available calibrations of kD(Fe-Mg) vs. T. The calculated TC values of both clino and orthopyroxenes were found to be close to the temperatures at which they were quenched, in line with expected kinetic behavior, when calibrations for cpx (Murri et al., 2016) and opx (Stimpfl et al., 2005) based on SC-XRD structure refinements were used. In particular, the smallest discrepancy between calculated and actual temperature is of the order of a few degrees (12 °C for cpx and 4 °C for opx), and the largest is of the order of tens of degrees (22 °C for cpx and 55 °C for opx). On the other hand, much lower TCs were obtained when calibrations based on Mössbauer determination of site occupancies were used. These results confirm that the two methods (i.e. SC-XRD and Mössbauer) give inherently different site occupancy data and that the same methodology should thus be used for both calibration and natural samples in the determination of cooling rate of host rocks.

PREDIKSI TEMPERATUR RESERVOAR PANASBUMI DENGAN MENGGUNAKAN METODA GEOTERMOMETER KIMIA FLUIDA

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Yoga Aribowo

2012-02-01

Full Text Available In the preliminary study of Geothermal field development, one the most important thing to observe istemperature capacity of the geothermal reservoirs. One of several method to get subsurface temperature datathat low cost and reliable is geothermometry method. With just surface investigation of the geothermal prospectand fluid geochemistry analysis, it is possible to make a prediction how hot reservoir fluids are. The subsurfacetemperature prediction is based on physical and chemical properties of some chemical constituent. Temperaturedependant solubility of many chemical consituent of geothermal fluids such as silica, chloride, and Na.

Oxygen isotope fractionation in uranium oxides

International Nuclear Information System (INIS)

Zheng Yongfei

1995-01-01

Thermodynamic oxygen isotope factors for uranium oxides have been calculated by means of the modified increment method. The sequence of 18 O-enrichment in the uranium oxides with respect to the common rock-forming minerals is predicted as follows: spinel 3 < illite. Two sets of self-consistent fractionation factors between the uranium oxides and water and between the uranium oxides and the other minerals have been obtained for 0∼1200 degree C. The theoretical results are applicable to the isotopic geothermometry of uranium ores when pairing with other gangue minerals in hydrothermal uranium deposits

Magma heating by decompression-driven crystallization beneath andesite volcanoes.

Science.gov (United States)

Blundy, Jon; Cashman, Kathy; Humphreys, Madeleine

2006-09-07

Explosive volcanic eruptions are driven by exsolution of H2O-rich vapour from silicic magma. Eruption dynamics involve a complex interplay between nucleation and growth of vapour bubbles and crystallization, generating highly nonlinear variation in the physical properties of magma as it ascends beneath a volcano. This makes explosive volcanism difficult to model and, ultimately, to predict. A key unknown is the temperature variation in magma rising through the sub-volcanic system, as it loses gas and crystallizes en route. Thermodynamic modelling of magma that degasses, but does not crystallize, indicates that both cooling and heating are possible. Hitherto it has not been possible to evaluate such alternatives because of the difficulty of tracking temperature variations in moving magma several kilometres below the surface. Here we extend recent work on glassy melt inclusions trapped in plagioclase crystals to develop a method for tracking pressure-temperature-crystallinity paths in magma beneath two active andesite volcanoes. We use dissolved H2O in melt inclusions to constrain the pressure of H2O at the time an inclusion became sealed, incompatible trace element concentrations to calculate the corresponding magma crystallinity and plagioclase-melt geothermometry to determine the temperature. These data are allied to ilmenite-magnetite geothermometry to show that the temperature of ascending magma increases by up to 100 degrees C, owing to the release of latent heat of crystallization. This heating can account for several common textural features of andesitic magmas, which might otherwise be erroneously attributed to pre-eruptive magma mixing.

Conodont geothermometry in pyroclastic kimberlite: constraints on emplacement temperatures and cooling histories

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Pell, Jennifer; Russell, James K.; Zhang, Shunxin

2018-03-01

Kimberlite pipes from Chidliak, Baffin Island, Nunavut, Canada host surface-derived Paleozoic carbonate xenoliths containing conodonts. Conodonts are phosphatic marine microfossils that experience progressive, cumulative and irreversible colour changes upon heating that are experimentally calibrated as a conodont colour alteration index (CAI). CAI values permit us to estimate the temperatures to which conodont-bearing rocks have been heated. Conodonts have been recovered from 118 samples from 89 carbonate xenoliths collected from 12 of the pipes and CAI values within individual carbonate xenoliths show four types of CAI distributions: (1) CAI values that are uniform throughout the xenolith; (2) lower CAIs in core of a xenolith than the rim; (3) CAIs that increase from one side of the xenolith to the other; and, (4) in one xenolith, higher CAIs in the xenolith core than at the rim. We have used thermal models for post-emplacement conductive cooling of kimberlite pipes and synchronous heating of conodont-bearing xenoliths to establish the temperature-time history of individual xenoliths within the kimberlite bodies. Model results suggest that the time-spans for xenoliths to reach the peak temperatures recorded by CAIs varies from hours for the smallest xenoliths to 2 or 3 years for the largest xenoliths. The thermal modelling shows the first three CAI patterns to be consistent with in situ conductive heating of the xenoliths coupled to the cooling host kimberlite. The fourth pattern remains an anomaly.

Geochemistry and hydrothermal alteration at selected Utah hot springs. Final report: Volume 3 (revised)

Energy Technology Data Exchange (ETDEWEB)

Parry, W.T.; Benson, N.L.; Miller, C.D.

1976-07-01

Application of Na-K-Ca geothermometry to warm springs in Utah indicates several areas with sufficiently high apparent temperatures to be of interest as geothermal exploration targets. A zone of warm springs in the Bonneville Basin show Na-K-Ca temperatures from 150/sup 0/C to 233/sup 0/C. Examination of Great Salt Lake, Bonneville sediment pore water, and Jordan Valley well-water chemistry indicates that mixing a small percent of these fluids with warm spring water can cause substantial errors in Na-K-Ca temperature estimates. Other saline deposits which may influence Na-K-Ca temperature estimates are the Paradox formation in southeastern Utah, the Muddy Creek formation in southwestern Utah, the Arapien shale in central Utah, the Preuss formation in northeastern Utah, and Playa salts in much of western Utah. The Roosevelt KGRA is the most attractive target identified by Na-K-Ca geothermometry. Hydrothermal alteration, heavy metal distribution, and water chemistry provide additional characterization of the Roosevelt system. Chemistry of a cool water seep (25/sup 0/C) shows Na-K-Ca temperature of 241/sup 0/C and SiO/sub 2/ temperature of 125/sup 0/C. A Phillips well flowing from below 1500' (457m) shows Na-K-Ca temperature of 262/sup 0/C, SiO/sub 2/ temperature of 262/sup 0/C, and K of 1.5 times the surface spring value. The near surface alteration assemblage is best explained in terms of a decrease in pH of near surface fluids as sulfide oxidizes. Increasing potassium and pH with depth indicates that a K-feldspar stable zone may be intersected with deeper drilling. Geology and alteration were mapped in the Monroe KGRA. (JGB)

Pre-eruptive conditions of dacitic magma erupted during the 21.7 ka Plinian event at Nevado de Toluca volcano, Central Mexico

Science.gov (United States)

Arce, J. L.; Gardner, J. E.; Macías, J. L.

2013-01-01

The Nevado de Toluca volcano in Central Mexico has been active over the last ca. 42 ka, during which tens of km3 of pyroclastic material were erupted and two important Plinian-type eruptions occurred at ca. 21.7 ka (Lower Toluca Pumice: LTP) and ca. 10.5 ka (Upper Toluca Pumice: UTP). Samples from both the LTP and UTP contain plagioclase, amphibole, iron-titanium oxides, and minor anhedral biotite, set in a vesicular, rhyolitic, glassy matrix. In addition, UTP dacites contain orthopyroxene. Analysis of melt inclusions in plagioclase phenocrysts yields H2O contents of 2-3.5 wt.% for LTP and 1.3-3.6 wt.% for UTP samples. Ilmenite-ulvospinel geothermometry yields an average temperature of ~ 868 °C for the LTP magma (hotter than the UTP magma, ~ 842 °C; Arce et al., 2006), whereas amphibole-plagioclase geothermometry yields a temperature of 825-859 °C for the LTP magma. Water-saturated experiments using LTP dacite suggest that: (i) amphibole is stable above 100 MPa and below 900 °C; (ii) plagioclase crystallizes below 250-100 MPa at temperatures of 850-900 °C; and (iii) pyroxene is stable only below pressures of 200-100 MPa and temperatures of 825-900 °C. Comparison of natural and experimental data suggests that the LTP dacitic magma was stored at 150-200 MPa (5.8-7.7 km below the volcano summit). No differences in pressure found between 21.7 ka and 10.5 ka suggest that these two magmas were stored at similar depths. Orthopyroxene produced in lower temperature LTP experiments is compositionally different to those found in UTP natural samples, suggesting that they originated in two different magma batches. Whole-rock chemistry, petrographic features, and mineral compositions suggest that magma mixing was responsible for the generation of the dacitic Plinian LTP eruption.

Application of thermodynamics to silicate crystalline solutions

Science.gov (United States)

Saxena, S. K.

1972-01-01

A review of thermodynamic relations is presented, describing Guggenheim's regular solution models, the simple mixture, the zeroth approximation, and the quasi-chemical model. The possibilities of retrieving useful thermodynamic quantities from phase equilibrium studies are discussed. Such quantities include the activity-composition relations and the free energy of mixing in crystalline solutions. Theory and results of the study of partitioning of elements in coexisting minerals are briefly reviewed. A thermodynamic study of the intercrystalline and intracrystalline ion exchange relations gives useful information on the thermodynamic behavior of the crystalline solutions involved. Such information is necessary for the solution of most petrogenic problems and for geothermometry. Thermodynamic quantities for tungstates (CaWO4-SrWO4) are calculated.

A conceptual geochemical model of the geothermal system at Surprise Valley, CA

Science.gov (United States)

Fowler, Andrew P. G.; Ferguson, Colin; Cantwell, Carolyn A.; Zierenberg, Robert A.; McClain, James; Spycher, Nicolas; Dobson, Patrick

2018-03-01

Characterizing the geothermal system at Surprise Valley (SV), northeastern California, is important for determining the sustainability of the energy resource, and mitigating hazards associated with hydrothermal eruptions that last occurred in 1951. Previous geochemical studies of the area attempted to reconcile different hot spring compositions on the western and eastern sides of the valley using scenarios of dilution, equilibration at low temperatures, surface evaporation, and differences in rock type along flow paths. These models were primarily supported using classical geothermometry methods, and generally assumed that fluids in the Lake City mud volcano area on the western side of the valley best reflect the composition of a deep geothermal fluid. In this contribution, we address controls on hot spring compositions using a different suite of geochemical tools, including optimized multicomponent geochemistry (GeoT) models, hot spring fluid major and trace element measurements, mineralogical observations, and stable isotope measurements of hot spring fluids and precipitated carbonates. We synthesize the results into a conceptual geochemical model of the Surprise Valley geothermal system, and show that high-temperature (quartz, Na/K, Na/K/Ca) classical geothermometers fail to predict maximum subsurface temperatures because fluids re-equilibrated at progressively lower temperatures during outflow, including in the Lake City area. We propose a model where hot spring fluids originate as a mixture between a deep thermal brine and modern meteoric fluids, with a seasonally variable mixing ratio. The deep brine has deuterium values at least 3 to 4‰ lighter than any known groundwater or high-elevation snow previously measured in and adjacent to SV, suggesting it was recharged during the Pleistocene when meteoric fluids had lower deuterium values. The deuterium values and compositional characteristics of the deep brine have only been identified in thermal springs and

Current status of thermoluminescence studies on minerals and rocks

International Nuclear Information System (INIS)

Sankaran, A.V.; Nambi, K.S.V.; Sunta, C.M.

1982-01-01

The usefulness of thermoluminescence (TL) in geological studies is being increasingly recognized, as may be judged from the considerable volume of literature accumulated over the past couple of decades; besides, a number of seminars, conferences and specialists' meetings have also been held on the subject of applied TL. However, these publications lie scattered over several periodicals and conference proceedings and an interested worker finds it difficult to obtain the gist of the contributions in one place. The present authors felt a need for this and have, therefore, attempted to bring together in this Report the current status of TL research about different minerals; applications in the fields of geochronology, ore-prospecting, stratigraphic correlation, geothermometry and other useful areas are also included. (author)

Carbon isotope geothermometry of graphite-bearing marbles from Central Dronning Maud Land, East Antarctica

International Nuclear Information System (INIS)

Wand, U.; Muehle, K.

1988-01-01

In order to estimate the peak metamorphic temperatures in high-grade regional metamorphic marbles from central Dronning Maud Land (East Antarctica), 13 C/ 12 C isotope ratios have been measured for coexisting carbonate and graphite pairs. The δ 13 C values of carbonates (calcite ± dolomite) and graphite vary from -0.1 to +4.6 permill (PDB) and from -3.3 to +1.7 permill, respectively. The isotopic fractionation between carbonate and graphite ranges from 2.9 to 4.0 permill and is similar to the Δ 13 C (carb-gr) values observed in other East Antarctic and non-Antarctic granulite-facies marbles. The metamorphic temperatures calculated using the equation of VALLEY and O'NEIL (1981) for calcite-graphite pairs are predominantly in the range 700 0 - 800 0 C (x n=5 ± s = 730 0 ± 30 0 C) and agree well with metamorphic temperatures derived from mineral chemical studies in this East Antarctic region. (author)

Deep Geothermal Reservoir Temperatures in the Eastern Snake River Plain, Idaho using Multicomponent Geothermometry

Energy Technology Data Exchange (ETDEWEB)

Ghanashyam Neupane; Earl D. Mattson; Travis L. McLing; Carl D. Palmer; Robert W. Smith; Thomas R. Wood

2014-02-01

The U.S. Geological survey has estimated that there are up to 4,900 MWe of undiscovered geothermal resources and 92,000 MWe of enhanced geothermal potential within the state of Idaho. Of particular interest are the resources of the Eastern Snake River Plain (ESRP) which was formed by volcanic activity associated with the relative movement of the Yellowstone Hot Spot across the state of Idaho. This region is characterized by a high geothermal gradient and thermal springs occurring along the margins of the ESRP. Masking much of the deep thermal potential of the ESRP is a regionally extensive and productive cold-water aquifer. We have undertaken a study to infer the temperature of the geothermal system hidden beneath the cold-water aquifer of the ESRP. Our approach is to estimate reservoir temperatures from measured water compositions using an inverse modeling technique (RTEst) that calculates the temperature at which multiple minerals are simultaneously at equilibrium while explicitly accounting for the possible loss of volatile constituents (e.g., CO2), boiling and/or water mixing. In the initial stages of this study, we apply the RTEst model to water compositions measured from a limited number of wells and thermal springs to estimate the regionally extensive geothermal system in the ESRP.

Fluid geochemistry and geothermometry applications of the Kangding high-temperature geothermal system in eastern Himalayas

International Nuclear Information System (INIS)

Guo, Qi; Pang, Zhonghe; Wang, Yingchun; Tian, Jiao

2017-01-01

High-temperature geothermal systems hold an enormous capacity for generating geothermal energy. The Kangding area is a typical high-temperature geothermal field in the Himalayan Geothermal Belt. Hydrogeochemical, gas geochemical and isotopic investigations were performed to identify and qualify the main hydrogeochemical processes affecting thermal water composition, including mixing and degassing, and then to estimate a reliable reservoir temperature. Nine water samples and four geothermal gas samples were collected and analysed for chemical and isotopic components. The results demonstrate the alkaline deep geothermal water is the mixtures of approximately 75% snow-melt water and 25% magmatic water. It is enriched in Na, K, F, Li and other trace elements, indicating the granite reservoir nature. The shallow geothermal water is the mixtures of approximately 30% upward flow of deep geothermal water and 70% meteoric cold water. High concentrations of Ca, Mg and HCO_3 indicate the limestone reservoir nature. There is no remarkable oxygen isotope shift in the geothermal water since the rapid circulation is difficult to trigger off strong water-rock interaction. CO_2 is the predominant geothermal gas, accounting for more than 97% of total gases in volume percentage. The concentration of CO_2 degassing ranged from 0.4 mol L"−"1 to 0.8 mol L"−"1 via geothermometrical modelling. As a result, the geothermal water pH increased from 6.0 to 9.0, and approximately 36% of the total SiO_2 re-precipitate. The sources of CO_2 are the metamorphism of limestone and magmatic degassing based on the composition of carbon isotope. The appropriate geothermometers of Na-K and Na-Li yield reservoir temperature of 280 °C. The geothermometrical modelling, developed to eliminate the effects of CO_2 degassing, yields temperature of 250 °C. The silica-enthalpy mixing model yields temperature of 270 °C with no steam separation before mixing. - Highlights: • Water and gas geochemical and isotopic differences between deep and shallow geothermal water. • Estimation of recharge sources and circulations for different geothermal waters. • Identification and qualification of main hydrogeochemical processes including mixing and degassing during the ascent of geothermal waters to the surface. • Comprehensive geothermometrical constraints for reservoir temperature in a very narrow range.

Origin of sulphur compounds and application of isotope geothermometry in selected geothermal systems of China

International Nuclear Information System (INIS)

Pang Zhonghe

2005-01-01

Geothermal and groundwater samples from East of Heber (EH) Province in the North China Basin and South of Fujian (SF) Province in Southeast of China were studied using sulphur and water isotopes. EH is located in a Mesozoic-Cenozoic sedimentary basin while SF is composed of small fault-block basins formed in Quaternary period. These systems belong to non-volcanic geothermal environments. Samples were collected from exploratory and production geothermal wells: 11 wells in EH and 17 wells in SF. The samples were analyzed for oxygen-18 (δ 18 O) and deuterium (δ 2 H) in water, sulfur-34 (δ 34 S) and oxygen-18 ((δ 18 O) in aqueous sulphate (SO 4 ). Chemical composition of the water samples was also determined. Results show that aqueous sulphate in the saline thermal waters of SF is of marine origin. The aqueous sulphate in EH waters is of non-marine origin. Reservoir temperature estimated using the oxygen isotope geothermometer is not compatible to those by chemical geothermometers or by down-hole measurements in the sedimentary environment for EH, different from that for the SF samples where aqueous sulphate seems to have reached equilibrium with thermal waters in the main up-flow zone. (author)

Mineralogy and geothermometry of high-temperature rhyolites from the central and western Snake River Plain

Science.gov (United States)

Honjo, N.; Bonnichsen, B.; Leeman, W.P.; Stormer, J.C.

1992-01-01

Voluminous mid-Miocene rhyolitic ash-flow tuffs and lava flows are exposed along the northern and southern margins of the central and western Snake River Plain. These rhyolites are essentially anhydrous with the general mineral assemblage of plagioclase ??sanidine ?? quartz + augite + pigeonite ?? hypersthene ?? fayalitic olivine + Fe-Ti oxides + apatite + zircon which provides an opportunity to compare feldspar, pyroxene, and Fe-Ti oxide equilibration temperatures for the same rocks. Estimated pyroxene equilibration temperatures (based on the geothermometers of Lindsley and coworkers) range from 850 to 1000??C, and these are well correlated with whole-rock compositions. With the exception of one sample, agreement between the two-pyroxene thermometers tested is well within 50??C. Fe-Ti oxide geothermometers applied to fresh magnetite and ilmenite generally yield temperatures about 50 to 100??C lower than the pyroxene temperatures, and erratic results are obtained if these minerals exhibit effects of subsolidus oxidation and exsolution. Results of feldspar thermometry are more complicated, and reflect uncertainties in the thermometer calibrations as well as in the degree of attainment of equilibrium between plagioclase and sanidine. In general, temperatures obtained using the Ghiorso (1984) and Green and Usdansky (1986) feldspar thermometers agree with the pyroxene temperatures within the respective uncertainties. However, uncertainties in the feldspar temperatures are the larger of the two (and exceed ??60??C for many samples). The feldspar thermometer of Fuhrman and Lindsley (1988) produces systematically lower temperatures for many of the samples studied. The estimated pyroxene temperatures are considered most representative of actual magmatic temperatures for these rhyolites. This range of temperatures is significantly higher than those for rhyolites from many other suites, and is consistent with the hypothesis that the Snake River Plain rhyolitic magmas formed by partial fusion of relatively dry (e.g. granulitic) crustal lithologies. ?? 1992 Springer-Verlag.

Chemistry and geothermometry of brine produced from the Salton Sea Scientific drill hole, Imperial Valley, California

Science.gov (United States)

Thompson, J.M.; Fournier, R.O.

1988-01-01

The December 29-30, 1985, flow test of the State 2-14 well, also known as the Salton Sea Scientific drill hole, produced fluid from a depth of 1865-1877 m at a reservoir temperature of 305????5??C. Samples were collected at five different flashing pressures. The brines are Na-Ca-K-Cl-type waters with very high metal and low SO4 and HCO3 contents. Compositions of the flashed brines were normalized relative to the 25??C densities of the solutions, and an ionic charge balance was achieved by adjusting the Na concentration. Calculated Na/K geothermometer temperatures, using equations suggested by different investigators, range from 326?? to 364??C. The Mg/K2 method gives a temperature of about 350??C, Mg/Li2 about 282??, and Na/Li 395??-418??C. -from Authors

A geochemical case history of the HGP-A well 1976-1982

International Nuclear Information System (INIS)

Thomas, D.M.

1982-01-01

The Hawaii Geothermal Project Well-A, located on the island of Hawaii, was completed in 1976 to a depth of 1966 meters. The bottomhole temperature, under shut-in conditions, is 360 0 C and at full discharge is capable of producing about 45,500 kg/hr of a mixed fluid composed of 48% steam and 52% liquid. The major element chemistry of the fluids suggests that recharge to the reservoir is largely fresh meteoric water with no more than 10% to 15% of the recharge being from sea water. Extensive water-rock equilibration has occured; however neither Na-K-Ca nor silica geothermometry calculations have been able to yield reasonable reservoir temperatures. Isotopic data suggest that the circulation rate and residence times of fluids in the reversoir are on the order of a few thousand years. Helium isotopic data also indicate that the heat source for this reservoir is very young or very large

Bibliographical review about Na/Li geo-thermometry and lithium isotopes applied to worldwide geothermal waters. Final report

International Nuclear Information System (INIS)

Sanjuan, B.; Millot, R.

2009-09-01

This study is performed within the framework of the FP6 European project HITI (High Temperature Instruments for supercritical geothermal reservoir characterization and exploitation). This research project, co-funded by EU and the different partners, aims to provide geophysical and geochemical sensors and methods to evaluate deep geothermal wells up to supercritical conditions (T > 370 deg. C), which are more cost-effective than those of the conventional wells. A deep geothermal well is currently being drilled for this purpose into the Krafla area, Iceland, as part of the IDDP ('Iceland Deep Drilling Project') and with joint funding from Icelandic industry and science Institutes. Another deep well will be drilled in the Reykjanes peninsula, Iceland, within the framework of the same project. This study, a bibliographical review about the Na/Li geo-thermometer and lithium isotopes applied on the world geothermal waters, is the first step of the task envisaged by BRGM to use and validate the sodium-lithium (Na-Li) chemical geo-thermometer on Icelandic geothermal waters at temperatures ranging from 25 to 500 deg. C. In this study, more than 120 temperature and chemical data from world geothermal and oil-fields, sedimentary basins, oceanic ridges, emerged rifts and island arcs have been collected and investigated. These additional data have allowed to confirm and refine the three existing Na/Li thermometric relationships. Moreover, a new Na/Li thermometric relationship relative to the processes of seawater or dilute seawater-basalt interaction occurring in the oceanic ridges and emerged rifts is proposed. Even if the running of Na/Li is still poorly understood, the existence of a new thermometric relationship confirms that the Na/Li ratios not only depend on the temperature but also on other parameters such as the fluid salinity and origin, or the nature of the reservoir rocks in contact with the geothermal fluids. For most of the geothermal waters in contact with volcanic rocks or granite in the deep reservoir, rock leaching and hydrothermal alteration (illite or smectite precipitation) are probably the main processes controlling the Li concentrations. Additional field and laboratory studies as well as a thermodynamic approach based on mineral dissolution-precipitation equilibrium reactions could help to support and confirm this assumption. The scarcity of the δ 7 Li values analysed in the geothermal and oil-field fluids and the presently available data indicate that it is necessary to acquire additional data in both fluids and rocks to better understand the Li behaviour in the processes of water-rock interaction. However, as the dissolved Li during these processes seems to be controlled by several influent factors, it is recommended to study the Li behaviour at different temperatures for a same type of process of water-rock interactions. Among possible applications, the determination of δ 7 Li values in geothermal waters shows that these data can be used to determine the nature of the reservoir rocks in contact with these waters and indirectly estimate the depth of these reservoirs. The Na/Li geo-thermometer, which is often less accurate than other classical geo-thermometers but can be more reliable in many cases, is then very useful for geothermal exploration. In order to improve the use of this geo-thermometer, additional developments in different environments and regions are necessary and it is essential to well define the environment in which it will be applied before its use. Experimental works in laboratory relative to water-rock interaction processes as a function of temperature integrating chemical, isotopic and mineralogical analyses should allow to improve the knowledge and to understand the running of this geo-thermometer. (authors)

The Effect of Element Substitution on Ti-in-Zircon Geothermometry in Volcanic Zircons from Mount Pinatubo, Philippines

Science.gov (United States)

Lee, S. L.; Hattori, K.

2017-12-01

Despite the extensive application of the Ti-in-zircon geothermometer, its accuracy in natural systems remains uncertain. In order to investigate the parameters contributing to Ti in zircon, we examined zircons from dacitic eruption products of Mount Pinatubo, Philippines, from the Pliocene (>2.5-2.7 Ma), 35000BP and 1991AD. All samples are unaltered and quenched from magmas at 790-825°C (Fe-Ti-oxide thermometry). Furthermore, the magma conditions of 1991 samples are well characterized: 780°C (cummingtonite rims on hornblende, Fe-Ti-oxide thermometry), 2 kbar pressure, 5.5-6.5 wt.% H2O and fO2 of NNO+1.6. Calculated zircon saturation temperatures are 760, 744 and 738°C (oldest to youngest). Zircon Ti concentrations are low (2.0-8.8 ppm), show positive covariation with U (35.6-639 ppm), Th (18.7-696 ppm), ∑REE (237-1310 ppm) and Y (247-1770 ppm), and negative covariation with Hf (7610-12000 ppm). The Ti-in-zircon geothermometer by Ferry and Watson (2007) yields mean temperatures of 690, 666 and 663°C (oldest to youngest), using TiO2 activity=0.6, SiO2 activity=1 and -40°C pressure correction. Therefore, temperatures calculated using this method are underestimated by >100°C. We suggest that elements in the Zr site impact the substitution of Ti in the Si site of zircon. Ti shows a positive covariation with Zr/Hf (37.0-57.3, r2=0.551). The ionic radius of Hf4+ is smaller than Zr4+, whereas cations like U4+, Th4+, REE3+ and Y3+ are larger. The departure from the ideal crystal configuration is evaluated using the parameter Zr/(Hf-x), whereby x=U4+, Th4+, ∑REE and Y3+. Ti contents are more strongly correlated with the parameter than Zr/Hf (r2=0.559, 0.565, 0.608, 0.616; respectively). This suggests that large cations replacing Zr strain the lattice, reducing the amount of Ti incorporated into zircon. This further suggests that ZrSiO4 activity is less than 1 in natural rocks, resulting in the systematic underestimation of Ti-in-zircon temperatures.

Bibliographical review about Na/Li geo-thermometry and lithium isotopes applied to worldwide geothermal waters. Final report

Energy Technology Data Exchange (ETDEWEB)

Sanjuan, B.; Millot, R.

2009-09-15

This study is performed within the framework of the FP6 European project HITI (High Temperature Instruments for supercritical geothermal reservoir characterization and exploitation). This research project, co-funded by EU and the different partners, aims to provide geophysical and geochemical sensors and methods to evaluate deep geothermal wells up to supercritical conditions (T > 370 deg. C), which are more cost-effective than those of the conventional wells. A deep geothermal well is currently being drilled for this purpose into the Krafla area, Iceland, as part of the IDDP ('Iceland Deep Drilling Project') and with joint funding from Icelandic industry and science Institutes. Another deep well will be drilled in the Reykjanes peninsula, Iceland, within the framework of the same project. This study, a bibliographical review about the Na/Li geo-thermometer and lithium isotopes applied on the world geothermal waters, is the first step of the task envisaged by BRGM to use and validate the sodium-lithium (Na-Li) chemical geo-thermometer on Icelandic geothermal waters at temperatures ranging from 25 to 500 deg. C. In this study, more than 120 temperature and chemical data from world geothermal and oil-fields, sedimentary basins, oceanic ridges, emerged rifts and island arcs have been collected and investigated. These additional data have allowed to confirm and refine the three existing Na/Li thermometric relationships. Moreover, a new Na/Li thermometric relationship relative to the processes of seawater or dilute seawater-basalt interaction occurring in the oceanic ridges and emerged rifts is proposed. Even if the running of Na/Li is still poorly understood, the existence of a new thermometric relationship confirms that the Na/Li ratios not only depend on the temperature but also on other parameters such as the fluid salinity and origin, or the nature of the reservoir rocks in contact with the geothermal fluids. For most of the geothermal waters in contact with volcanic rocks or granite in the deep reservoir, rock leaching and hydrothermal alteration (illite or smectite precipitation) are probably the main processes controlling the Li concentrations. Additional field and laboratory studies as well as a thermodynamic approach based on mineral dissolution-precipitation equilibrium reactions could help to support and confirm this assumption. The scarcity of the {delta}{sup 7}Li values analysed in the geothermal and oil-field fluids and the presently available data indicate that it is necessary to acquire additional data in both fluids and rocks to better understand the Li behaviour in the processes of water-rock interaction. However, as the dissolved Li during these processes seems to be controlled by several influent factors, it is recommended to study the Li behaviour at different temperatures for a same type of process of water-rock interactions. Among possible applications, the determination of {delta}{sup 7}Li values in geothermal waters shows that these data can be used to determine the nature of the reservoir rocks in contact with these waters and indirectly estimate the depth of these reservoirs. The Na/Li geo-thermometer, which is often less accurate than other classical geo-thermometers but can be more reliable in many cases, is then very useful for geothermal exploration. In order to improve the use of this geo-thermometer, additional developments in different environments and regions are necessary and it is essential to well define the environment in which it will be applied before its use. Experimental works in laboratory relative to water-rock interaction processes as a function of temperature integrating chemical, isotopic and mineralogical analyses should allow to improve the knowledge and to understand the running of this geo-thermometer. (authors)

Geothermometry, geochronology, and mass transfer associated with hydrothermal alteration of a rhyolitic hyaloclastite from Ponza Island, Italy

Science.gov (United States)

Altaner, S.P.; Ylagan, R.F.; Savin, S.M.; Aronson, J.L.; Belkin, H.E.; Pozzuoli, A.

2003-01-01

A rhyolitic hyaloclastite from Ponza Island, Italy, was hydrothermally altered, producing four distinct alteration zones based on X-ray diffraction mineralogy and field textures: (1) nonpervasive argillic zone; (2) propylitic zone; (3) silicic zone; and (4) sericitic zone. The unaltered hyaloclastite is volcanic breccia with clasts of vesiculated obsidian in a matrix of predominantly pumice lapilli. Incomplete alteration of the hyaloclastite resulted in the nonpervasive argillic zone, characterized by smectite and disordered opal-CT. The other three zones exhibit more complete alteration of the hyaloclastite. The propylitic zone is characterized by mixed-layer illite-smectite (I-S) with 10 to 85% I, mordenite, opal-C, and authigenic K-feldspar (akspar). The silicic zone is characterized by I-S with ???90% I, pure illite, quartz, akspar, and occasional albite. The sericitic zone consists primarily of I-S with ???66% I, pure illite, quartz, and minor akspar and pyrite. K/Ar dates of I-S indicate hydrothermal alteration occurred at 3.38 ?? 0.08 Ma. Oxygen isotope compositions of I-S systematically decrease from zones 1 to 4. In the argillic zone, smectite has ??18 O values of 21.7 to 22.0??? and I-S from the propylitic, silicic, and sericitic zones ranges from 14.5 to 16.3???, 12.5 to 14.0???, and 8.6 to 11.9???, respectively. ??18 O values for quartz from the silicic and sericitic zones range from 12.6 to 15.9???. By use of isotope fractionation equations and data from authigenic quartz-hosted primary fluid inclusions, alteration temperatures ranged from 50 to 65 ??C for the argillic zone, 85 to 125 ??C for the propylitic zone, 110 to 210 ??C for the silicic zone, and 145 to 225 ??C for the sericitic zone. Fluid inclusion data and calculated ??18 O water values indicate that hydrothermal fluids were seawater dominated. Mass-transfer calculations indicate that hydrothermal alteration proceeded in a relatively open chemical system and alteration in the sericitic zone involved the most extensive loss of chemical species, especially Si. Systematic gains in Mg occur in all alteration zones as a result of I-S clay mineral formation, and systematic losses of Na, Ca, and K occur in most zones. With the exception of Ca, calculations of mass transfer associated with hydrothermal alteration on Ponza agree with chemical fluxes observed in laboratory experiments involving hydrothermal reactions of rhyolite and seawater. The anomalous Ca loss at Ponza may be due to hydrothermal formation of anhydrite and later low-temperature dissolution. On the basis of Mg enrichments derived from circulating seawater, we estimate the following minimum water/rock ratios: 9, 3, 6, and 9 for the argillic, propylitic, silicic, and sericitic zones, respectively. Hydrothermal fluid pH for the propylitic and silicic zones was neutral to slightly basic and relatively acidic for the sericitic zone as a result of condensation of carbonic and perhaps other acids. Copyright ?? 2003 Elsevier Science Ltd.

Constraints on the depositional age and tectonometamorphic evolution of marbles from the Biharia Nappe System (Apuseni Mountains, Romania

Directory of Open Access Journals (Sweden)

Reiser Martin Kaspar

2017-04-01

Full Text Available Basement rocks from the Biharia Nappe System in the Apuseni Mountains comprise several dolomite and calcite marble sequences or lenses which experienced deformation and metamorphic overprint during the Alpine orogeny. New Sr, O and C-isotope data in combination with considerations from the lithological sequences indicate Middle to Late Triassic deposition of calcite marbles from the Vulturese-Belioara Series (Biharia Nappe s.str.. Ductile deformation and large-scale folding of the siliciclastic and carbonatic lithologies is attributed to NW-directed nappe stacking during late Early Cretaceous times (D2. The studied marble sequences experienced a metamorphic overprint under lower greenschist- facies conditions (316-370 °C based on calcite - dolomite geothermometry during this tectonic event. Other marble sequences from the Biharia Nappe System (i.e. Vidolm and Baia de Arieș nappes show similarities in the stratigraphic sequence and their isotope signature, together with a comparable structural position close to nappe contact. However, the dataset is not concise enough to allow for a definitive attribution of a Mesozoic origin to other marble sequences than the Vulturese-Belioara Series.

Rock geochemistry related to mineralization processes in geothermal areas

Science.gov (United States)

Kausar, A. Al; Indarto, S.; Setiawan, I.

2018-02-01

Abundant geothermal systems in Indonesia suggest high heat and mass transfer associated with recent or paleovolcanic arcs. In the active geothermal system, the upflow of mixed fluid between late stage hydrothermal and meteoric water might contain mass of minerals associated with epithermal mineralisation process as exemplified at Lihir gold mine in Papua New Guinea. In Indonesia, there is a lack of study related to the precious metals occurrence within active geothermal area. Therefore, in this paper, we investigate the possibility of mineralization process in active geothermal area of Guci, Central Java by using geochemical analysis. There are a lot of conducted geochemical analysis of water, soil and gas by mapping the temperature, pH, Hg and CO2 distribution, and estimating subsurface temperature based on geothermometry approach. Then we also apply rock geochemistry to find minerals that indicate the presence of mineralization. The result from selected geothermal area shows the presence of pyrite and chalcopyrite minerals on the laharic breccias at Kali Putih, Sudikampir. Mineralization is formed within host rock and the veins are associated with gold polymetallic mineralization.

Variations of geothermometry and chemical-isotopic compositions of hot spring fluids in the Rehai geothermal field, southwestern China

Science.gov (United States)

Du, Jianguo; Liu, Congqiang; Fu, Bihong; Ninomiya, Yoshiki; Zhang, Youlian; Wang, Chuanyuan; Wang, Hualiu; Sun, Zigang

2005-04-01

Geothermal variations, origins of carbon-bearing components and reservoir temperatures in the Rehai geothermal field (RGF) of Tengchong volcanic area, Yunnan Province, southwestern China, are discussed on the basis of carbon isotope compositions, combined with helium isotope ratios and geothermal data from 1973 to 2000. δ 13C values of CO 2, CH 4, HCO 3-, CO 3= and travertine in the hot springs range from -7.6‰ to -1.18‰, -56.9‰ to -19.48‰, -6.7‰ to -4.2‰, -6.4‰ to -4.2‰ and -27.1‰ to +0.6‰, respectively. The carbon dioxide probably has a mantle/magma origin, but CH 4 and He have multiple origins. HCO 3- and CO 3= in RGF thermal fluids are predominantly derived from igneous carbon dioxide, but other ions originate from rocks through which the fluids circulate. The 13C values of CO 2, HCO 3- (aq) and CO 3= (aq) illustrate that isotopic equilibriums between CO 2 and HCO 3- (aq), and CO 3= (aq) and between DIC and travertine were not achieved, and no carbon isotope fractionation between HCO 3- (aq) and CO 3= (aq) of the hot springs in RGF was found. Using various geothermometers, temperatures of the geothermal reservoirs are estimated in a wide range from 69 °C to 450 °C that fluctuated from time to time. The best estimate of subsurface reservoir temperature may be 250-300 °C. Contributions of mantle fluids and shallow crust fluids in Rehai geothermal field varied with time, which resulted in variations of chemical and isotopic compositions and reservoir temperatures.

Geothermometry obtained from the calcite twin and fluid inclusions in barite (Irankuh Pb-Zn deposit, Southwest of Isfahan

Directory of Open Access Journals (Sweden)

Alijan Aftabi

2017-03-01

Full Text Available The Irankuh mining district is located 20 km southwest of Isfahan and is geologically situated in Sanandaj - Sirjan zone and the lower Cretaceous sequence of Isfahan-Malayer ore mineralization area. The ore minerals are emplaced in the faulted contact of Jurassic shale and Cretaceous carbonates and include pyrite, galena, sphalerite, calcite, barite, dolomite, quartz as well as minor marcasite, smithsonite, cerussite, gypsum, malachite, hematite and goethite. The mineralization is mainly occurred as hydrothermal veins and veinlets associated with fractures and faults, suggesting the deposit is likely to be of epigenetic type. A comparison between geothermometric results obtained from calcite twins and fluid inclusions showed a similar temperature range for the mineralization (less than 170ºc. Fluid inclusion studies indicate the temperature, salinity and density ranges of 80-166ºc, 5.39-20.94 wt.% NaCl and 0.95-1.12, respectively. The obtained data share many similarities with those of the MVT deposits

Geothermometry obtained from the calcite twin and fluid inclusions in barite (Irankuh Pb-Zn deposit, Southwest of Isfahan)

OpenAIRE

Alijan Aftabi; Hengameh Hosseini-Dinani

2017-01-01

The Irankuh mining district is located 20 km southwest of Isfahan and is geologically situated in Sanandaj - Sirjan zone and the lower Cretaceous sequence of Isfahan-Malayer ore mineralization area. The ore minerals are emplaced in the faulted contact of Jurassic shale and Cretaceous carbonates and include pyrite, galena, sphalerite, calcite, barite, dolomite, quartz as well as minor marcasite, smithsonite, cerussite, gypsum, malachite, hematite and goethite. The mineralization is mainly occu...

Silicate geothermometry as an indicator of water-rock interaction processes in the serpentinized mafic-ultramafic intrusion of Ylivieska

International Nuclear Information System (INIS)

Ruskeeniemi, T.; Blomqvist, R.; Vuorela, P.; Frape, S.K.; Blyth, A.

1996-01-01

The aim of the study was to use oxygen and hydrogen isotopes to examine the origin of different generations of serpentine. Of special interest was the study of low-temperature generations that may be correlated with the present meteoric waters. The research was commenced with drill core logging in order to obtain insight into the fracture minerals and their distribution in a mafic-ultramafic intrusion. (39 refs., 17 figs., 5 tabs.)

Hydrogeochemistry and geothermometry of deep thermal water in the carbonate formation in the main urban area of Chongqing, China

Science.gov (United States)

Yang, Pingheng; Cheng, Qun; Xie, Shiyou; Wang, Jianli; Chang, Longran; Yu, Qin; Zhan, Zhaojun; Chen, Feng

2017-06-01

Many geothermal reservoirs in Chongqing in southwestern China are located in carbonate rock aquifers and exploited through drilling. Water samples from 36 geothermal wells have been collected in the main urban area of Chongqing. Chemical types of the thermal water samples are Ca·Mg-SO4 and Ca-SO4. High contents of Ca2+ and SO42- in the thermal water samples are derived from the dissolution of evaporates. Furthermore, the HCO3- concentration is constrained by the common ion effect. Drilling depth has no effect on the physical and chemical characteristics according to the results of a t-test. The geothermal reservoir's temperature can be estimated to be 64.8-93.4 °C (average 82 °C) using quartz and improved SiO2 geothermometers. Values of δD and δ18O for the thermal water samples indicate that the thermal water resources originate from local precipitation with a recharge elevation between 838 and 1130 m and an annual air temperature between 10.4 and 13.9 °C. A conceptual model of regional scale groundwater flow for the thermal water is proposed. The thermal water mainly originates from the meteoric water recharged in the elevated areas of northeastern Tongluoshan and Huayingshan by means of percolation through exposed carbonate before becoming groundwater. The groundwater is heated at depth and moves southwest along the fault and the anticlinal core in a gravity-driven regime. The thermal water is exposed in the form of artesian hot springs in river cutting and low-elevation areas or in wells.

Origin, evolution and geothermometry of the thermal waters in the Gölemezli Geothermal Field, Denizli Basin (SW Anatolia, Turkey)

Science.gov (United States)

Alçiçek, Hülya; Bülbül, Ali; Brogi, Andrea; Liotta, Domenico; Ruggieri, Giovanni; Capezzuoli, Enrico; Meccheri, Marco; Yavuzer, İbrahim; Alçiçek, Mehmet Cihat

2018-01-01

The Gölemezli Geothermal Field (GGF) is one of the best known geothermal fields in western Anatolia (Turkey). The exploited fluids are of meteoric origin, mixed with deep magmatic fluids, which interacted with the metamorphic rocks of the Menderes Massif. The geothermal fluids are channeled along Quaternary faults belonging to the main normal faults system delimiting the northern side of the Denizli Basin and their associated transfer zones. In this study, hydrochemical and isotopic analyses of the thermal and cold waters allow us to determine water-rock interactions, fluid paths and mixing processes. Two groups of thermal waters have been distinguished: (i) Group 1A, comprising Na-SO4 type and Ca-SO4 type and (ii) Group 1B, only consisting Ca-HCO3 type waters. Differently, two groups were recognized in the cold waters: (i) Group 2A, corresponding to Ca-HCO3 type and (ii) Group 2B, including Mg-HCO3 type. Their geochemical characteristics indicate interactions with the Paleozoic metamorphic rocks of the Menderes Massif and with the Neogene lacustrine sedimentary rocks. Dissolution of host rock and ion-exchange reactions modify thermal water composition in the reservoir of the GGF. High correlation in some ionic ratios and high concentrations of some minor elements suggest an enhanced water-rock interaction. None of the thermal waters has been reached a complete chemical re-equilibrium, possibly as a result of mixing with cold water during their pathways. Geothermal reservoir temperatures are calculated in the range of 130-210°C for the Gölemezli field. Very negative δ18O and δ2H isotopic ratios are respectively between -8.37 and -8.13‰ and -61.09 and -59.34‰ for the SO4-rich thermal waters, and ca. - 8.40 and -8.32‰ and - 57.80 and -57.41‰ for the HCO3-rich thermal waters. Low tritium (link existing between fractures and fluid convection in the extensional settings. In this view, the GGF is a very good example of geothermal field associated to active tectonic setting and magmatism, as it is the case of the other geothermal fields occurring in the Denizli Basin.

Resource investigation of low- and moderate-temperature geothermal areas in Paso Robles, California

Energy Technology Data Exchange (ETDEWEB)

Campion, L.F.; Chapman, R.H.; Chase, G.W.; Youngs, L.G.

1983-01-01

Ninety-eight geothermal wells and springs were identified and plotted, and a geologic map and cross sections were compiled. Detailed geophysical, geochemical, and geological surveys were conducted. The geological and geophysical work delineated the basement highs and trough-like depressions that can exercise control on the occurrence of the thermal waters. The Rinconada fault was also evident. Cross sections drawn from oil well logs show the sediments conforming against these basement highs and filling the depressions. It is along the locations where the sediments meet the basement highs that three natural warm springs in the area occur. Deep circulation of meteoric waters along faults seems to be a reasonable source for the warm water. The Santa Margarita, Pancho Rico, and Paso Robles Formations would be the first permeable zones that abut the faults through which water would enter. Temperatures and interpretation of well logs indicate the warmest aquifer at the base of the Paso Robles Formation. Warm water may be entering higher up in the section, but mixing with water from cooler zones seems to be evident. Geothermometry indicates reservoir temperatures could be as high as 91/sup 0/C (196/sup 0/F).

Geology of the Pavana geothermal area, Departamento de Choluteca, Honduras, Central America: Field report

Energy Technology Data Exchange (ETDEWEB)

Eppler, D.B.; Heiken, G.; Wohletz, K.; Flores, W.; Paredes, J.R.; Duffield, W.A.

1987-09-01

The Pavana geothermal area is located in southern Honduras near the Gulf of Fonseca. This region is underlain by late Tertiary volcanic rocks. Within ranges near the geothermal manifestations, the rock sequences is characterized by intermediate to mafic laharic breccias and lavas overlain by silicic tuffs and lavas, which are in turn overlain by intermediate to mafic breccias, lavas, and tuffs. The nearest Quaternary volcanoes are about 40 km to the southwest, where the chain of active Central American volcanoes crosses the mouth of the Gulf of Fonseca. Structure of the Pavana area is dominated by generally northwest-trending, southwest-dipping normal faults. This structure is topographically expressed as northwest-trending escarpments that bound blocks of bedrock separated by asymmetric valleys that contain thin alluvial deposits. Thermal waters apparently issue from normal faults and are interpreted as having been heated during deep circulation along fault zones within a regional environment of elevated heat flow. Natural outflow from the main thermal area is about 3000 l/min of 60/sup 0/C water. Geothermometry of the thermal waters suggests a reservoir base temperature of about 150/sup 0/C.

Assembling of a low energy ion beam analysis facility and use of Nuclear Microprobe techniques in geological studies

International Nuclear Information System (INIS)

Utui, R.

1996-11-01

In this work, both PIXE and ion beam induced luminescence, or just Ionoluminescence (IL) were used for geochemical studies. The possibility of rapid absolute quantification of elements in the ppm level by PIXE combined with the yet higher sensitivity of IL to transition metals and Rare Earth Elements (REE) activators, in the absence of quenching phenomena, allow for a synergic use of the two methods in geological applications with enhanced sensitivity. IL and PIXE were combined for studying REE distribution in apatite minerals and ion beam induced damage in inorganic material in general with emphasis to synthetically grown zircon crystals doped with REE. Due to the sensitivity of IL to changes in chemical bonding in the material, beam damage effects can be studied even at low integrated doses, through wavelength shift or fading of the induced light. Micro PIXE technique was used for studying profile concentrations of trace elements in pyrite grains and of elements used as geothermometers. Geothermometry allowed to assess the cooling rates in iron meteorites and the mineralization conditions in metamorphic rocks, attempting to describe the tectonic history of the terranes, with application in petrologic studies and geological prospecting. 148 refs

Assembling of a low energy ion beam analysis facility and use of Nuclear Microprobe techniques in geological studies

Energy Technology Data Exchange (ETDEWEB)

Utui, R

1996-11-01

In this work, both PIXE and ion beam induced luminescence, or just Ionoluminescence (IL) were used for geochemical studies. The possibility of rapid absolute quantification of elements in the ppm level by PIXE combined with the yet higher sensitivity of IL to transition metals and Rare Earth Elements (REE) activators, in the absence of quenching phenomena, allow for a synergic use of the two methods in geological applications with enhanced sensitivity. IL and PIXE were combined for studying REE distribution in apatite minerals and ion beam induced damage in inorganic material in general with emphasis to synthetically grown zircon crystals doped with REE. Due to the sensitivity of IL to changes in chemical bonding in the material, beam damage effects can be studied even at low integrated doses, through wavelength shift or fading of the induced light. Micro PIXE technique was used for studying profile concentrations of trace elements in pyrite grains and of elements used as geothermometers. Geothermometry allowed to assess the cooling rates in iron meteorites and the mineralization conditions in metamorphic rocks, attempting to describe the tectonic history of the terranes, with application in petrologic studies and geological prospecting. 148 refs.

Oxygen isotope exchange rate between dissolved sulfate and water at hydrothermal temperatures

International Nuclear Information System (INIS)

Chiba, H.; Sakai, H.

1985-01-01

Oxygen isotope exchange rate between dissolved sulfate and water was experimentally determined at 100, 200 and 300 deg C. The isotope exchange rate is strongly dependent on temperature and pH of the solution. Combining the temperature and pH dependence of the reaction rate, the exchange reaction was estimated to be first-order with respect to sulfate. The logarithm of apparent rate constant of exchange reaction at a given temperature is a function of the pH calculated at the experimental temperatures. From the pH dependence of the apparent rate constant, it was deduced that the isotope exchange reaction between dissolved sulfate and water proceeds through collision between H 2 SO 4 0 and H 2 O at low pH, and between HSO 4 - and H 2 O at intermediate pH. The isotope exchange rate obtained indicates that oxygen isotope geothermometry utilizing the studied isotope exchange is suitable for temperature estimation of geothermal reservoirs. The extrapolated half-life of this reaction to oceanic temperature is about 10 9 years, implying that exchange between oceanic sulfate and water cannot control the oxygen isotope ratio of oceanic sulfates. (author)

Near-surface clay authigenesis in exhumed fault rock of the Alpine Fault Zone (New Zealand); O-H-Ar isotopic, XRD and chemical analysis of illite and chlorite

Science.gov (United States)

Boles, Austin; Mulch, Andreas; van der Pluijm, Ben

2018-06-01

Exhumed fault rock of the central Alpine Fault Zone (South Island, New Zealand) shows extensive clay mineralization, and it has been the focus of recent research that aims to describe the evolution and frictional behavior of the fault. Using Quantitative X-ray powder diffraction, 40Ar/39Ar geochronology, hydrogen isotope (δD) geochemistry, and electron microbeam analysis, we constrain the thermal and fluid conditions of deformation that produced two predominant clay phases ubiquitous to the exposed fault damage zone, illite and chlorite. Illite polytype analysis indicates that most end-member illite and chlorite material formed in equilibrium with meteoric fluid (δD = -55 to -75‰), but two locations preserve a metamorphic origin of chlorite (δD = -36 to -45‰). Chlorite chemical geothermometry constrains crystal growth to T = 210-296 °C. Isotopic analysis also constrains illite growth to T < 100 °C, consistent with the mineralogy, with Ar ages <0.5 Ma. High geothermal gradients in the study area promoted widespread, near-surface mineralization, and limited the window of clay authigenesis in the Alpine Fault Zone to <5 km for chlorite and <2 km for illite. This implies a significant contrast between fault rock exposed at the surface and that at depth, and informs discussions about fault strength, clays and frictional behavior.

A Geological and Geophysical Study of the Geothermal Energy Potential of Pilgrim Springs, Alaska

Energy Technology Data Exchange (ETDEWEB)

Turner, Donald L.; Forbes, Robert B. [eds.

1980-01-01

The Pilgrim Springs geothermal area, located about 75 km north of Nome, was the subject of an intensive, reconnaissance-level geophysical and geological study during a 90-day period in the summer of 1979. The thermal springs are located in a northeast-oriented, oval area of thawed ground approximately 1.5 km{sup 2} in size, bordered on the north by the Pilgrim River. A second, much smaller, thermal anomaly was discovered about 3 km northeast of the main thawed area. Continuous permafrost in the surrounding region is on the order of 100 m thick. Present surface thermal spring discharge is {approx} 4.2 x 10{sup -3} m{sup 3} s{sup -1} (67 gallons/minute) of alkali-chloride-type water at a temperature of 81 C. The reason for its high salinity is not yet understood because of conflicting evidence for seawater vs. other possible water sources. Preliminary Na-K-Ca geothermometry suggests deep reservoir temperatures approaching 150 C, but interpretation of these results is difficult because of their dependence on an unknown water mixing history. Based on these estimates, and present surface and drill hole water temperatures, Pilgrim Springs would be classified as an intermediate-temperature, liquid-dominated geothermal system.

Geochemistry of Precambrian carbonatite complexes of India : present status of, and gaps in our knowledge

Energy Technology Data Exchange (ETDEWEB)

Udas, G R [Department of Atomic Energy, Hyderabad (India). Atomic Minerals Div.

1974-01-01

Carbonatites of Precambrian age occur at Newania and Mundwara in Rajasthan, Sevathur and Hogenakal in Tamil Nadu, Kunavaram in Andhra Pradesh, and Kollegal in Karnataka. The Newia carvonatite is 952 +- 24 m.v. old (K-Ar age of an alkali amplibole), and the Sevathur carbontite is 720 +- 30 m.y. old (K-Ar age of a biotite). Although comprehensive geochemical studies involving major, minor, and trace elements, and carbon, oxygen and strontium isotopes have been undertaken on the 37.5 +- 2.5 m.y. old Eocene carbonatite complex at Amba Dongar, Gujarat, geochemical studies on the Precambrian carbonatites of India have been confined only to routine determinations of selected elements like Sr, Ba, Y, Ce, La, Nb, Zr, Th, Mn, Ti, F and P to demonstrate their carbonatitic affinites. Except for two K-Ar ages, and for some limited trace element data, no attempts have been made to elucidate the chronologic and petrogenetic evolution of these Precambrian carbonatites by the application of Rb-Sr, K-Ar, and U-Pb geochronometry, critical element ratios, stable and radiogenic isotope abundances, and geothermometry. Basic researches aimed at formulating geochemical criteria for locating commercially exploitable economic Precambrian carbonatite complexes are yet to be initiated in India. (auth)

Oxygen isotope studies of the Salton Sea geothermal field

International Nuclear Information System (INIS)

Olson, E.R.

1978-01-01

Interbedded shales and sandstones were drilled to a depth of 1588 metres in Sinclair Number Four Well, Salton Sea Geothermal Field. Bottom hole temperatures are approximately 290 0 C. The oxygen dels of hydrothermal and detrital calcite have a systematic relationship at any depth in the geothermal reservoir. Typical values are: vein calcite, +6 0 / 00 ; calcite in white sandstone, +10 0 / 00 ; calcite in dark gray shale, +11 0 / 00 ; calcite in light gray shale, +17 0 / 00 ; calcite in red-brown shale, +20 0 / 00 . This succession represents decreasing water-rock interaction that is also indicated by the clay mineralogy of the shales. Permeability has a marked effect on the equilibration of water and rocks at any given temperature. Original differences in permeability have resulted in partial preservation of original detrital sedimentary compositions. The fluids in the Salton Sea Geothermal Field are probabaly partially evaporated Colorado River water, and their oxygen del values vary as much as 4 0 / 00 throughout the field. Truesdell's (1974) data suggest that dissolved salts may make the water oxygen activity del as much as 6 0 / 00 greater than the concentration del in the geothermal reservoir. Such an uncertainty is a serious impediment to precise isotope geothermometry in this system.(auth.)

Crystal chemistry of iron in low-temperature chlorites, implications for geo-thermometry and the determination of redox paleo-conditions in uranium deposits

International Nuclear Information System (INIS)

Rigault, Cecile

2010-01-01

In contexts of uranium deposits, redox conditions constitute the main factor controlling the uranium deposition. Often observed in these deposits, chlorites are the unique clay mineral which can be able to record in their structure the redox conditions through their Fe"3"+/SFe ratio. However, the common presence of several populations of chlorites makes difficult to understand the message carried out by these minerals. Thanks to μ-XANES spectroscopy, we are now able to measure on thin sections the Fe"3"+/SFe ratio in chlorites with an accuracy of 5 %. Measurements show that it can reach 60 % in di-tri-octahedral chlorites and 5 % to more than 40 % for tri-octahedral chlorites. In hydrothermal contexts where chlorites crystallize through a dissolution-recrystallization process, their Fe"3"+/SFe ratio decreases with the increase of the global Fe content. Diagenetic chlorites observed resulting from the polymorphic transformation of berthierine have a different behavior because there is no link between their total iron content and their Fe"3"+/SFe ratio: their chemistry is directly inherited from the one of the precursor mineral because this transformation does not allow a reorganization of cations in the structure. This transformation explains that thermodynamic models cannot work for these phases. For the use of chlorites as makers of redox paleo-conditions in contexts of uranium deposits where diagenetic and hydrothermal chlorites can be present, it is decisive to determine their origin, for example analyzing their polytype: Ib (b=90 degrees) for chlorites crystallized from solid-state transformation and IIb for chlorites crystallized through dissolution-recrystallization process. (author)

Solute geochemistry of the Snake River Plain regional aquifer system, Idaho and eastern Oregon

International Nuclear Information System (INIS)

Wood, W.W.; Low, W.H.

1987-01-01

Three geochemical methods were used to determine chemical reactions that control solute concentrations in the Snake River Plain regional aquifer system: (1) calculation of a regional solute balance within the aquifer and of mineralogy in the aquifer framework to identify solute reactions, (2) comparison of thermodynamic mineral saturation indices with plausible solute reactions, and (3) comparison of stable isotope ratios of the groundwater with those in the aquifer framework. The geothermal groundwater system underlying the main aquifer system was examined by calculating thermodynamic mineral saturation indices, stable isotope ratios of geothermal water, geothermometry, and radiocarbon dating. Water budgets, hydrologic arguments, and isotopic analyses for the eastern Snake River Plain aquifer system demonstrate that most, if not all, water is of local meteoric and not juvenile or formation origin. Solute balance, isotopic, mineralogic, and thermodynamic arguments suggest that about 20% of the solutes are derived from reactions with rocks forming the aquifer framework. Reactions controlling solutes in the western Snake river basin are believed to be similar to those in the eastern basin but the regional geothermal system that underlies the Snake river Plain contains total dissolved solids similar to those in the overlying Snake River Plain aquifer system but contains higher concentrations of sodium, bicarbonate, silica, fluoride, sulfate, chloride, arsenic, boron, and lithium, and lower concentrations of calcium, magnesium, and hydrogen. 132 refs., 30 figs., 27 tabs

Geochemical and petrological study of the anphibolites from Cassia Region, MG

International Nuclear Information System (INIS)

Correia, C.T.; Girardi, V.A.V.

1989-01-01

The orthoamphibolites of the Cassia Region, Minas Gerais State, belong to two different groups distinguished by their TiO 2 contents (average contents 2.67% respectively). (La, Nb, V, Zr, Ce, and Zn). The titanium-poor group is slightly enriched in SiO 2 . The remarkable differences in incompatible element ratios between ATi and BTi(e.g., 4-,5 and 11-fold for Ce/Y, Zr/Nb and Y/La, respectively) indicate that the parent basaltic rocks of both groups were not derived either by fractional crystallizatin or by partial melting from a homogeneous source. It is suggested that the parent basilitic rocks of ATi and BTi were related to chemically hetrogeneous mantles materials. The clear discrimination of both groups in the Ti-Zr-Y diagram is attributed to geochemical characteristics of their genesis and does not necessarily indicate different environments. Metamorphic grade in the Cassia region increases from SSW to NNE. In the amphibolites, progresssive metamorphism is indicated by increase in the anorthite content of plagioclase; by changes of colour and composition of the amphiboles, which vary from tschermakitic hornblendes (green) to edenitic hornblendes (brownish-green to brown); and by increase in the pyrope content of garnet. The temperatures obtained through geothermometry of the amplhibolities vary from 650 0 C to slightly greater than 725 0 C. Minimum pressures are estimated around 6.5Kb [pt

Evolution of the Cerro Prieto geothermal system as interpreted from vitrinite reflectance under isothermal conditions

Energy Technology Data Exchange (ETDEWEB)

Barker, C.E. (US Geological Survey, Denver, CO); Pawlewicz, M.J.; Bostick, N.H.; Elders, W.A.

1981-01-01

Temperature estimates from reflectance data in the Cerro Prieto system correlate with modern temperature logs and temperature estimates from fluid inclusion and oxygen isotope geothermometry indicating that the temperature in the central portion of the Cerro Prieto System is now at its historical maximum. Isoreflectance lines formed by contouring vitrinite reflectance data for a given isothermal surface define an imaginary surface that indicates an apparent duration of heating in the system. The 250/sup 0/C isothermal surface has a complex dome-like form suggesting a localized heat source that has caused shallow heating in the central portion of this system. Isoreflectance lines relative to this 250/sup 0/C isothermal surface define a zone of low reflectance roughly corresponding to the crest of the isothermal surface. Comparison of these two surfaces suggest that the shallow heating in the central portion of Cerro Prieto is young relative to the heating (to 250/sup 0/C) on the system margins. Laboratory and theoretical models of hydrothermal convection cells suggest that the form of the observed 250/sup 0/C isothermal surface and the reflectance surface derived relative to it results from the convective rise of thermal fluids under the influence of a regional hydrodynamic gradient that induces a shift of the hydrothermal heating effects to the southwest.

Mineralogy, fluid inclusion petrography, and stable isotope geochemistry of Pb-Zn-Ag veins at the Shizhuyuan deposit, Hunan Province, southeastern China

Science.gov (United States)

Wu, Shenghua; Mao, Jingwen; Yuan, Shunda; Dai, Pan; Wang, Xudong

2018-01-01

The Shizhuyuan polymetallic deposit is located in the central part of the Nanling region, southeastern China, and consists of proximal W-Sn-Mo-Bi skarns and greisens and distal Pb-Zn-Ag veins. The sulfides and sulfosalts in the distal veins formed in three distinct stages: (1) an early stage of pyrite and arsenopyrite, (2) a middle stage of sphalerite and chalcopyrite, and (3) a late stage of galena, Ag-, Sn-, and Bi-bearing sulfides and sulfosalts, and pyrrhotite. Combined sulfide and sulfosalt geothermometry and fluid inclusion analyses indicate that the early stage of mineralization occurred at a temperature of 400 °C and involved boiling under hydrostatic pressure ( 200 bar), with the temperature of the system dropping during the late stage to 200 °C. Laser Raman analysis indicates that the fluid inclusions within the studied minerals are dominated by H2O, although some contain carbonate solids and CH4 gas. Vein-hosted sulfides have δ34S values of 3.8-6.3‰ that are interpreted as indicative of a magmatic source of sulfur. The mineralization process can be summarized as follows: an aqueous fluid exsolved on final crystallization of the Qianlishan pluton, ascended along fracture zones, cooled to <400 °C, and boiled under hydrostatic conditions, and with decreasing temperature and sulfur fugacity, sulfide and sulfosalt minerals precipitated successively from the Ag-Cu-Zn-Fe-Pb-Sb-As-S-bearing fluid system.

Origin of fumarolic fluids from Tupungatito Volcano (Central Chile): interplay between magmatic, hydrothermal, and shallow meteoric sources

Science.gov (United States)

Benavente, Oscar; Tassi, Franco; Gutiérrez, Francisco; Vaselli, Orlando; Aguilera, Felipe; Reich, Martin

2013-08-01

Tupungatito is a poorly known volcano located about 100 km eastward of Santiago (Chile) in the northernmost sector of the South Volcanic Zone. This 5,682 m high volcano shows intense fumarolic activity. It hosts three crater lakes within the northwestern portion of the summit area. Chemical compositions of fumarolic gases and isotopic signatures of noble gases (3He/4He and 40Ar/36Ar are up to 6.09 Ra and 461, respectively), and steam (δ18O and δD) suggest that they are produced by mixing of fluids from a magmatic source rich in acidic gas compounds (SO2, HCl, and HF), and meteoric water. The magmatic-hydrothermal fluids are affected by steam condensation that controls the outlet fumarolic temperatures (contamination from the subducting slab, (2) the sedimentary basement, and (3) limited contribution from crustal sediments. Gas geothermometry based on the kinetically rapid H2-CO equilibria indicates equilibrium temperatures 200 °C and redox conditions are consistent with those inferred by the presence of the SO2-H2S redox pair, typical of fluids that have attained equilibrium in magmatic environment. A comprehensive conceptual geochemical model describing the circulation pattern of the Tupungatito hydrothermal-magmatic fluids is proposed. It includes fluid source regions and re-equilibration processes affecting the different gas species due to changing chemical-physical conditions as the magmatic-hydrothermal fluids rise up toward the surface.

Origins of secondary silica within Yucca Mountain, Nye County, southwestern Nevada

International Nuclear Information System (INIS)

Moscati, R.J.; Whelan, J.F.

1996-01-01

The accuracy of predictions of the hydrologic response of Yucca Mountain to future climate depends largely on how well relations between past climate and hydrology can be resolved. To advance this reconstruction, secondary minerals in and near Yucca Mountain, deposited by ground waters that originated both as surficial recharge at Yucca Mountain and from regional aquifers, are being studied to determine past ground-water sources and chemistries. Preliminary data on stable oxygen isotopes indicate that, although silica (opal, quartz, and chalcedony) and calcite and have formed in similar settings and from somewhat similar fluids, the authors have found no compelling evidence of coprecipitation or formation from identical fluids. If verified by further analyses, this precludes the use of silica-calcite mineral pairs for precise geothermometry. The preliminary data also indicate that opal and calcite occurrences in pedogenic and unsaturated-zone settings are invariably compatible with formation under modern ambient surface or subsurface temperatures. Silica and calcite stable-isotope studies are being integrated with soil geochemical modeling. This modeling will define the soil geochemical condition (climate) leading to opal or calcite deposition and to the transfer functions that may apply at the meteorologic soil unsaturated-zone interfaces. Additional study of pedogenic and unsaturated-zone silica is needed to support these models. The hypothesis that the transformation of vapor-phase tridymite to quartz requires saturated conditions is being tested through stable oxygen-isotope studies of lithophysal tridymite/quartz mixtures. Should this hypothesis be verified, mineralogic analysis by X-ray diffraction theoretically would permit reconstruction of past maximum water-table elevations

Heat flow at the Platanares, Honduras, geothermal site

Science.gov (United States)

Meert, Joseph G.; Smith, Douglas L.

1991-03-01

Three boreholes, PLTG-1, PLTG-2 and PLTG-3, were drilled in the Platanares, Honduras geothermal system to evaluate the geothermal energy potential of the site. The maximum reservoir temperature was previously estimated at 225-240°C using various types of chemical and isotopic geothermometry. Geothermal gradients of 139-239°C/km, calculated from two segments of the temperature-depth profile for borehole PLTG-2, were used to project a minimum depth to the geothermal reservoir of 1.2-1.7 km. Borehole PLTG-1 exhibited an erratic temperature distribution attributed to fluid movement through a series of isolated horizontal and subhorizontal fractures. The maximum measured temperature in borehole PLTG-1 was 150.4°C, and in PLTG-2 the maximum measured temperature was 104.3°C. PLTG-3 was drilled after this study and the maximum recorded temperature of 165°C is similar to the temperature encountered in PLTG-1. Heat flow values of 392 mWm -2 and 266 mWm -2 represent the first directly-measured heat flow values for Honduras and northen Central America. Radioactive heat generation, based on gamma-ray analyses of uranium, thorium and potassium in five core samples, is less than 2.0 μWm -3 and does not appear to be a major source of the high heat flow. Several authors have proposed a variety of extensional tectonic environments for western Honduras and these heat flow values, along with published estimates of heat flow, are supportive of this type of tectonic regime.

Petrology of the 1995/2000 Magma of Copahue, Argentina

Science.gov (United States)

Goss, A.; Varekamp, J. C.

2001-05-01

Phreatomagmatic eruptions of Copahue in July/August,1995 and July/August 2000 produced mixed juvenile clasts, silica-rich debris from the hydrothermal system, and magmatic scoria with 88 percent SiO2. These high-SiO2 clasts carry an as yet unidentified (crystobalite?), euhedral silica phase in great abundance, which is riddled with tan, primary melt inclusions. The mixed clasts have bands of mafic material with small euhedral olivine, clinopyroxene, and plagioclase that are mixed with an intermediate magma with coarser, resorbed phenocrysts of olivine, plagioclase, clino- and ortho- pyroxene, and rare occurrences of the silica phase. These ejecta are intimate mixtures of a relatively felsic magma similar to Pleistocene Copahue lavas and a mafic basaltic andesite, with minor contributions of a magma contaminated with silica-rich hydrothermal wallrock material. Two-pyroxene geothermometry indicates crystallization temperatures of 1020 deg - 1045 deg C. Glass inclusions (59-63 percent SiO2) in plagioclase and olivine crystals yield very low volatile contents in the melt (0.4-1.5 percent H2O). The 1995/2000 magmas resided at shallow level and degassed into the active volcano-hydrothermal system which discharges acid fluids into the Copahue crater lake and hot springs. More mafic magma intruded this shallow batch and the mixture rose into the hydrothermal system and assimilated siliceous wall rock. A Ti-diffusion profile in a magnetite crystal suggests that the period between magma mixing and eruption was on the order of 4-10 weeks, and the temperature difference between resident and intruding magma was about 50-60 oC.

Experimental cation redistribution in the tourmaline lucchesiite, CaFe2 + 3Al6(Si6O18)(BO3)3(OH)3O

Science.gov (United States)

Bosi, Ferdinando; Skogby, Henrik; Hålenius, Ulf; Ciriotti, Marco E.

2018-02-01

Natural Mg-rich lucchesiite was thermally treated in air and hydrogen atmosphere up to 800 °C to study potential changes in Fe-, Mg- and Al ordering over the octahedrally coordinated Y- and Z-sites, and to explore possible applications to intracrystalline geothermometry based on tourmaline. Overall, the experimental data (structural refinement, Mössbauer, infrared and optical absorption spectroscopy) show that thermal treatment of lucchesiite results in an increase of Fetot contents at Z balanced by an increase of Mg and Al at Y. This process is accompanied by a significant deprotonation of the O3 anion site. The Fe order-disorder reaction depends more on temperature, than on redox conditions. During heat treatment in H2, reduction of Fe3+ to Fe2+ was not observed despite strongly reducing conditions, indicating that the f O2 conditions do not exclusively control the Fe oxidation state at the present experimental conditions. On the basis of this and previous studies, the intersite order-disorder process induced by thermal treatment indicates that Fe redistribution is an important factor for Fe-Mg-Al-exchange and is significant at temperatures around 800 °C. As a result, Fe-Mg-Al intersite order-disorder is sensitive to temperature variations, whereas geothermometers based solely on Mg-Al order-disorder appear insensitive and involve large uncertainties. The presented findings are important for interpretation of the post-crystallization history of both tourmaline and tourmaline host rocks, and indicate that successful tourmaline geothermometers may be developed by thermal calibration of the Fe-Mg-Al order-disorder reaction.

Thermal waters along the Konocti Bay fault zone, Lake County, California: a re-evaluation

Science.gov (United States)

Thompson, J.M.; Mariner, R.H.; White, L.D.; Presser, T.S.; Evans, William C.

1992-01-01

The Konocti Bay fault zone (KBFZ), initially regarded by some as a promising target for liquid-dominated geothermal systems, has been a disappointment. At least five exploratory wells were drilled in the vicinity of the KBFZ, but none were successful. Although the Na-K-Ca and Na-Li geothermometers indicate that the thermal waters discharging in the vicinity of Howard and Seigler Springs may have equilibrated at temperatures greater than 200??C, the spring temperatures and fluid discharges are low. Most thermal waters along the KBFZ contain >100 mg/l Mg. High concentrations of dissolved magnesium are usually indicative of relatively cool hydrothermal systems. Dissolution of serpentine at shallow depths may contribute dissolved silica and magnesium to rising thermal waters. Most thermal waters are saturated with respect to amorphous silica at the measured spring temperature. Silica geothermometers and mixing models are useless because the dissolved silica concentration is not controlled by the solubility of either quartz or chalcedony. Cation geothermometry indicates the possibility of a high-temperature fluid (> 200??C) only in the vicinity of Howard and Seigler Springs. However, even if the fluid temperature is as high as that indicated by the geothermometers, the permeability may be low. Deuterium and oxygen-18 values of the thermal waters indicate that they recharged locally and became enriched in oxygen-18 by exchange with rock. Diluting meteoric water and the thermal water appear to have the same deuterium value. Lack of tritium in the diluted spring waters suggest that the diluting water is old. ?? 1992.

DYNAMIC MIXING MODEL OF THE CHIGNAHUAPAN THERMAL SPRING IN THE GEOTHERMAL ZONE OF THE ACOCULCO CALDERA, PUEBLA, MEXICO

Science.gov (United States)

Gutierrez-Cirlos, A.; Torres-Rodriguez, V.

2009-12-01

The Acoculco Caldera, of Pliocenic age, is located within the limits of the Transmexican Volcanic Belt (CVT) and the Sierra Madre Oriental (SMOr). The Acoculco geothermal zone consists of a 790m thick igneous sequence, related to a volcanic complex formed by andesites and rhyolitic domes emplaced in an 18 Km diameter annular fracture. It unconformably overlies a 5000 m thick section of folded and faulted Jurassic-Cretaceous carbonate rocks. The Chignahuapan Spring, located in the extreme eastern part of the Geothermal Zone of the Acoculco Caldera, yields temperatures of 49°C and discharges an estimated of 98 lps from the karstified Lower Cretaceous limestone. Both major and trace element geochemical analysis were carried out, and results were interpreted using Piper and Stiff diagrams, as well as geothermometry. The results indicate that water belongs to the calcium-bicarbonate type and yield temperatures in a range of 70-80°C at depth, which suggest an extensive lateral flow from the main reservoir and mixing with shallow groundwaters. The spring suffers significant variations in its temperature throughout the year, especially during the rainy season, when water temperature decreases up to 10°C. Analyzing the hot spring water temperature data from of the last 10 years and comparing it with the precipitation and air temperature curves of the region, we expect to develop a dynamic mixing model which depicts the relation between these factors and the importance of each one in the water temperature variation. We also look forward to be able to forecast water temperature trends for the next several years and correlate it with climate change in the area.

Final Scientific/Technical Report – DE-EE0002960 Recovery Act. Detachment faulting and Geothermal Resources - An Innovative Integrated Geological and Geophysical Investigation of Pearl Hot Spring, Nevada

Energy Technology Data Exchange (ETDEWEB)

Stockli, Daniel F. [Univ. of Texas, Austin, TX (United States)

2015-11-30

The Pearl Host Spring Geothermal Project funded by the DoE Geothermal Program was a joint academic (KU/UT & OU) and industry collaboration (Sierra and Ram Power) to investigate structural controls and the importance of low-angle normal faults on geothermal fluid flow through a multifaceted geological, geophysical, and geochemical investigation in west-central Nevada. The study clearly showed that the geothermal resources in Clayton Valley are controlled by the interplay between low-angle normal faults and active deformation related to the Walker Lane. The study not only identified potentially feasible blind geothermal resource plays in eastern Clayton Valley, but also provide a transportable template for exploration in the area of west-central Nevada and other regional and actively-deforming releasing fault bends. The study showed that deep-seated low-angle normal faults likely act as crustal scale permeability boundaries and could play an important role in geothermal circulation and funneling geothermal fluid into active fault zones. Not unique to this study, active deformation is viewed as an important gradient to rejuvenated fracture permeability aiding the long-term viability of blind geothermal resources. The technical approach for Phase I included the following components, (1) Structural and geological analysis of Pearl Hot Spring Resource, (2) (U-Th)/He thermochronometry and geothermometry, (3) detailed gravity data and modeling (plus some magnetic and resistivity), (4) Reflection and Refraction Seismic (Active Source), (5) Integration with existing and new geological/geophysical data, and (6) 3-D Earth Model, combining all data in an innovative approach combining classic work with new geochemical and geophysical methodology to detect blind geothermal resources in a cost-effective fashion.

Insights from gas and water chemistry on the geothermal system of the Domuyo volcanic complex (Patagonia, Argentina)

Science.gov (United States)

Tassi, F.; Liccioli, C.; Chiodini, G.; Agusto, M.; Caselli, A. T.; Caliro, S.; Vaselli, O.; Pecoraino, G.

2015-12-01

This study focuses on the geochemistry of geothermal fluids discharging from the western flank of the Domuyo volcanic complex (Argentina), which is hosted within an extensional basins that interrupts the Andes at latitudes comprises between 35° and 39°S. The analytical results of gas and water samples collected during three sampling campaigns (2013, 2014 and 2015) are presented and discussed in order to: i) evaluate the equilibrium temperature(s) of the main fluid reservoir, ii) provide information on the origin of the fluid discharges and the secondary processes controlling their chemistry. Geothermometry based on the chemical composition of thermal waters indicates a maximum equilibrium temperature of 220 °C. This temperature, coupled with the measured amount of discharged Cl, suggest that the total energy released from this system is 1.1±0.2 GW. Atmospheric gases from a thick shallow aquifer contaminate most gas emissions, masking the chemical features of the deep fluid component, with the only exception of a jet fumarole located at 3,000 m a.s.l. (Bramadora). The H2O-CO2-CH4-H2-CO-C3H6-C3H8 composition of this gas emission was used to construct a geochemical conceptual model showing that the hydrothermal reservoir is liquid-dominated and thermally stratified, with temperatures ranging from 180 to 270 °C. The helium isotopic ratios (up to 6.8 Ra) and the δ13C-CO2 values (from -7.05 to -7.75 ‰ V-PDB) indicate that mantle degassing represents the dominant primary source for this dormant volcano. These results highlight the huge potential of this system as energy resource for the region. Accordingly, the regional authorities have recently planned and approved an investigation project aimed to provide further insights into the fluid geochemistry and the geostructural assessment in this promising area.

Petrographic study and preliminary conceptual model of the Ixtlan de los Hervores geothermal zone, Michoacan, Mexico; Estudio petrografico y modelo conceptual preliminar de la zona geotermica de Ixtlan de los Hervores, Michoacan, Mexico

Energy Technology Data Exchange (ETDEWEB)

Viggiano-Guerra, Julio C; Gutierrez-Negrin, Luis C.A [Comision Federal de Electricidad (Mexico)

2007-10-15

Petrographic studies of cuttings from the shallow well Ixtlan 2, drilled in the Ixtlan de los Hervores geothermal zone, State of Michoacan, Mexico, at a maximum depth of 159 meters, together with results of previous exploration studies, allow to delineate a preliminary conceptual model of the probable geothermal system. It is formed by a wide-fracture zone system, with low topographic relief and shallow water level. Its hydrothermal fluids are of sodium-chloride type, neutral pH, silica oversaturated in the discharge and with temperatures between 125 and 225 degrees Celsius, based on the geothermometry and the hydrothermal mineral assemblage encountered in the well. The assemblage of laumontite + quartz + calcite + chlorite/smectite + pyrite is typical for the zeolitic facies, beneath of which it is possible to encounter the epidote-wairakite facies, with higher temperatures. The favorable conditions of the zone allow to recommend continuation of exploration in the same. [Spanish] El estudio petrografico de muestras de canal de la perforacion del pozo somero Ixtlan 2, con una profundidad maxima de 159 metros y ubicado en la zona geotermica de Ixtlan de Los Hervores, Michoacan, Mexico, aunado a los resultados de estudios previos de exploracion superficial, han permitido la configuracion de un modelo conceptual preliminar del probable yacimiento geotermico. Se trata de un sistema zona de fractura ancha, bajo relieve y nivel freatico somero, con fluidos hidrotermales de tipo clorurado-sodico, pH neutro, sobresaturados de silice en la descarga, y con temperatura entre 125 y 225 grados Celsius, de acuerdo con la geotermometria + cuarzo + calcita + clorita/esmectita + pirita es tipica de la facies zeolitica, debajo de la cual podria hallarse la facies de epidota-wairakita, con temperaturas mas altas. Las condiciones favorables de la zona permiten recomendar la continuacion de la exploracion en la misma.

Potential for a significant deep basin geothermal system in Tintic Valley, Utah

Science.gov (United States)

Hardwick, C.; Kirby, S.

2014-12-01

The combination of regionally high heat flow, deep basins, and permeable reservoir rocks in the eastern Great Basin may yield substantial new geothermal resources. We explore a deep sedimentary basin geothermal prospect beneath Tintic Valley in central Utah using new 2D and 3D models coupled with existing estimates of heat flow, geothermometry, and shallow hydrologic data. Tintic Valley is a sediment-filled basin bounded to the east and west by bedrock mountain ranges where heat-flow values vary from 85 to over 240 mW/m2. Based on modeling of new and existing gravity data, a prominent 30 mGal low indicates basin fill thickness may exceed 2 km. The insulating effect of relatively low thermal conductivity basin fill in Tintic Valley, combined with typical Great Basin heat flow, predict temperatures greater than 150 °C at 3 km depth. The potential reservoir beneath the basin fill is comprised of Paleozoic carbonate and clastic rocks. The hydrology of the Tintic Valley is characterized by a shallow, cool groundwater system that recharges along the upper reaches of the basin and discharges along the valley axis and to a series of wells. The east mountain block is warm and dry, with groundwater levels just above the basin floor and temperatures >50 °C at depth. The west mountain block contains a shallow, cool meteoric groundwater system. Fluid temperatures over 50 °C are sufficient for direct-use applications, such as greenhouses and aquaculture, while temperatures exceeding 140°C are suitable for binary geothermal power plants. The geologic setting and regionally high heat flow in Tintic Valley suggest a geothermal resource capable of supporting direct-use geothermal applications and binary power production could be present.

Back-arc basalts from the Loncopue graben (Province of Neuquen, Argentina)

Science.gov (United States)

Varekamp, J. C.; Hesse, A.; Mandeville, C. W.

2010-11-01

Young basaltic back-arc volcanoes occur east of the main Andes chain at about 37.5°-39°S in the Loncopue graben, Province of Neuquen, Argentina. These olivine-rich basalts and trachybasalts have up to 8% MgO, with high Ni and Cr contents, but highly variable incompatible element concentrations. Mafic lava flows and cinder cones at the southern end of the graben lack phenocrystic plagioclase. The northern samples have relative Ta-Nb depletions and K, Pb and LREE enrichment. These samples strongly resemble rocks of the nearby arc volcanoes Copahue and Caviahue, including their Fe-Ti enrichment relative to the main Andes arc rocks. The Sr, Nd and Pb isotope ratios show that the source regions of these back-arc basalts are enriched in subducted components that were depleted in the aqueous mobile elements such as Cs, Sr and Ba as a result of prior extractions from the subducted complex below the main arc. Some mafic flows show slightly low 206Pb/ 204Pb and 143Nd/ 144Nd values as well as incompatible trace element ratios similar to southern Patagonia plateau back-arc basalts, suggesting contributions from an EM1 mantle source. Geothermometry and barometry suggest that the basalts crystallized and fractionated small amounts of olivine and spinel at ˜ 35 km depth at temperatures of 1170-1220 °C, at about QFM + 0.5 to QFM + 1 with 1-2% H 2O, and then rose rapidly to the surface. The Loncopue graben back-arc basalts are transitional in composition between the South Patagonia back-arc plateau basalts and the Caviahue and Copahue arc volcanoes to the northwest. The EM1 source endmember is possibly the subcontinental lithospheric mantle. Strong variations in incompatible element enrichment and isotopic compositions between closely spaced cinder cones and lava flows suggest a heterogeneous mantle source for the Loncopue graben volcanics.

Current and future geothermal research in New Zealand

International Nuclear Information System (INIS)

Graham, I.J.; Browne, P.; Christenson, B.W.; Hunt, T.M.; Weir, G.

2000-01-01

Research programs by Crown Research Institutes (Geological and Nuclear Sciences Ltd. and Industrial Research Ltd.), university departments (Auckland, Massey and Victoria), power companies and private consultancies aim to obtain a better understanding of currently producing geothermal fields in New Zealand, and of deep geothermal systems which might have potential for future resource development. Research is also being directed at industrial and environmental issues related to exploitation, water-rock alteration processes, changes in shallow geothermal systems with time, and mineralisation as it relates to epithermal ore formation. The chemical and physical environment of geothermal reservoirs in the Taupo Volcanic Zone (e.g. Thames, Kawerau, Ohaaki, Ngatamariki, Wairakei, Tongariro, Tauhara and Tokaanu-Waihi) is being quantified with the aim of developing a suite of magma to ambient production scenarios using numerical, reactive transport models. A variety of geological, geochemical and geophysical techniques including fluid inclusion geothermometry, stable isotope analysis, electromagnetic, micro-seismic and magnetotelluric analysis is providing high quality input data. Through experimentation and computer modelling, criteria for assessing the optimal depths for re-injection of production effluents are being developed, and related problems such as silica and calcite scaling, pipeline insulation and chemical corrosion investigated. Paths, flow mechanisms and flow rates of re-injection plumes are being modelled using electrical resistivity, micro-gravity and radioisotope tracer methods. Environmental effects related to testing and development, presently causing concern amongst local authorities and the public, are being quantitatively assessed, and recommendations made to mitigate them. The mechanical and petrological properties of rocks in shallow aquifers undergoing ground subsidence are being determined, and the extent and style of ground deformation investigated

Granitoid-associated gold mineralization in Egypt: a case study from the Atalla mine

Science.gov (United States)

Zoheir, Basem; Deshesh, Fatma; Broman, Curt; Pitcairn, Iain; El-Metwally, Ahmed; Mashaal, Shabaan

2018-06-01

Gold-bearing sulfide-quartz veins cutting mainly through the Atalla monzogranite intrusion in the Eastern Desert of Egypt are controlled by subparallel NE-trending brittle shear zones. These veins are associated with pervasive sericite-altered, silicified, and ferruginated rocks. The hosting shear zones are presumed as high-order structures of the Najd-style faults in the Central Eastern Desert ( 615-585 Ma). Ore minerals include an early pyrite-arsenopyrite (±pyrrhotite) mineralization, partly replaced by a late pyrite-galena-sphalerite-chalcopyrite (±gold/electrum ± tetrahedrite ± hessite) assemblage. Gold occurs as small inclusions in pyrite and arsenopyrite, or more commonly as intergrowths with galena and sphalerite/tetrahedrite in microfractures. Arsenopyrite geothermometry suggests formation of the early Fe-As-sulfide mineralization at 380-340 °C, while conditions of deposition of the late base metal-gold assemblage are assumed to be below 300 °C. Rare hessite, electrum, and Bi-galena are associated with sphalerite and gold in the late assemblage. The early and late sulfide minerals show consistently a narrow range of δ34S ‰ (3.4-6.5) that overlaps with sulfur isotopic values in ophiolitic rocks. The Au-quartz veins are characterized by abundant CO2 and H2O ± CO2 ± NaCl inclusions, where three-dimensional clusters of inclusions show variable aqueous/carbonic proportions and broad range of total (bimodal) homogenization temperatures. Heterogeneous entrapment of immiscible fluids is interpreted to be caused by unmixing of an originally homogenous, low salinity ( 2 eq. mass % NaCl) aqueous-carbonic fluid, during transition from lithostatic to hydrostatic conditions. Gold deposition occurred generally under mesothermal conditions, i.e., 1.3 kbar and 280 °C, and continued during system cooling to chemistry of the ore fluids.

Magnetic properties and phase transformations of iron sulfides synthesized under the hydrothermal method

Science.gov (United States)

Li, S. H.; Chen, Y. H.

2016-12-01

The iron sulfide nano-minerals possess advantages of high abundance, low cost, and low toxicity. These advantages make them be competitive in the magnetic, electronic, and photoelectric applications. Mackinawite can be used in soil or water remediations. Greigite is very important for paleomagnetic and geochemical environment studies and the anode materials for lithium ion batteries. Besides, greigite is also utilized for hyperthermia and biomedicine. Pyrrhotite can be applied as geothermometry. Due to the above-mentioned reasons, iron sulfide minerals have specific significances and they must be further investigated, like their phase transformations, magnetic properties, and etc. In this study, the iron sulfide minerals were synthesized by using a hydrothermal method. The ex-situ and in-situ X-ray diffraction (XRD) was used to examine the crystal structure and phase transformation of iron sulfide minerals. The Transmission electron microscopy (TEM) and superconducting quantum interference device (SQUID) were carried out to investigate their morphology and magnetic properties, respectively. The results suggested that the phase transformation sequence was followed the order: mackinawite → greigite → (smythite) → pyrrhotite. Two pure mineral phases of greigite and pyrrhotite were obtained under the hydrothermal conditions. The morphology of the pure greigite is granular aggregates with a particle size of approximately 30 nm and pyrrhotite presented a hexagonal sheet stacking with a particle size of thousands nanometers. The greigite had a ferri-magnetic behavior and pyrrhotite was weak ferro-magnetic. Both of them had a pseudo-single magnetic domain (PSD) based on the Day's plot from SQUID data. The complete phase-transformation pathways and high magnetization of iron sulfide minerals are observed in this study and these kind of iron sulfide minerals are worthy to further study.

Deep groundwater circulation and associated methane leakage in the northern Canadian Rocky Mountains

International Nuclear Information System (INIS)

Grasby, S.E.; Ferguson, G.; Brady, A.; Sharp, C.; Dunfield, P.; McMechan, M.

2016-01-01

Concern over potential impact of shale gas development on shallow groundwater systems requires greater understanding of crustal scale fluid movement. We examined natural deeply circulating groundwater systems in northeastern British Columbia adjacent to a region of shale gas development, in order to elucidate origin of waters, depths of circulation, and controls on fluid flow. These systems are expressed as thermal springs that occur in the deformed sedimentary rocks of the Liard Basin. Stable isotope data from these springs show that they originate as meteoric water. Although there are no thermal anomalies in the region, outlet temperatures range from 30 to 56 °C, reflecting depth of circulation. Based on aqueous geothermometry and geothermal gradients, circulation depths up to 3.8 km are estimated, demonstrating connection of deep groundwater systems to the surface. Springs are also characterised by leakage of thermogenic gas from deep strata that is partly attenuated by methanotrophic microbial communities in the spring waters. Springs are restricted to anomalous structural features, cross cutting faults, and crests of fault-cored anticlines. On a regional scale they are aligned with the major tectonic features of the Liard Line and Larsen Fault. This suggests that while connection of surface to deep reservoirs is possible, it is rare and restricted to highly deformed geologic units that produce permeable pathways from depth through otherwise thick intervening shale units. Results allow a better understanding of potential for communication between deep shale gas units and shallow aquifer systems. - Highlights: • Deep groundwater systems were studied near active shale gas development. • Natural fracture systems allow circulation of meteoric water to depths of 3.8 km. • Deep circulation systems occur, but are rare in even highly deformed rocks.

Modes and implications of mantle and lower-crust denudation at slow-spreading mid-ocean ridges

Science.gov (United States)

Schroeder, Timothy John

Slow-spreading mid-ocean ridges (Cann, 1993, Cannat, 1993). Extension at mid-ocean ridges is most commonly manifested by slip on high angle (˜60°) normal faults that dip into, and define the rift valley walls (Smith and Cann, 1993). Less commonly, extension occurs by long periods of slip along low-angle normal faults that penetrate to structurally deep levels of oceanic lithosphere and denude gabbro and/or pendotite to the seafloor in domal massifs termed "oceanic core complexes" (Dick et al., 1981; Dick et al., 1991; Tucholke et al., 1998; Mutter and Karson, 1992; Cann et al., 1997; MacLeod et al., 2002). This dissertation addresses processes and implications of tectonic extension at two oceanic core complexes. Atlantis Massif (30°N, Mid-Atlantic Ridge) is formed dominantly of serpentinized peridotite with lesser gabbro, and Atlantis Bank (57°E, Southwest Indian Ridge) is dominated by gabbro. Localization of brittle strain at Atlantis Massif occurred by reaction-softening processes associated with metasomatic alteration of peridotite and serpentmite to amphibole-, chlorite- and talc-bearing assemblages. Ductile strain at Atlantis Massif and Atlantis Bank is localized into intervals of highly-fractionated, oxide-rich gabbro. Two-oxide geothermometry of gabbro indicates that it was not penetratively deformed below ˜500°C. Denuded peridotite at Atlantis Massif is host to hydrothermal circulation driven in part by exothermic serpentinization reactions. Serpentinization decreases the seismic velocity of peridotite and leads to acquisition of a magnetic signature. Venting of highly-alkaline, methane- and hydrogen-rich serpentinization-derived fluids leads to lithification of seafloor carbonate ooze by precipitation of carbonate cement in a zone of mixing with "normal" seawater. This process may be the primary depositional mechanism of ophicalcite deposits and likely occurs wherever peridotite is exposed near the Earth's surface and is fractured to permit water

Decompression Induced Crystallization of Basaltic Andesite Magma: Constraints on the Eruption of Arenal Volcano, Costa Rica.

Science.gov (United States)

Szramek, L. A.; Gardner, J. E.; Larsen, J. F.

2004-12-01

Arenal Volcano is a small stratovolcano located 90 km NW of San Jose, Costa Rica. In 1968 current activity began with a Plinian phase, and has continued to erupt lava flows and pyroclastic flows intermittently since. Samples from the Plinian, pyroclastic flow, strombolian, and effusive phases have been studied texturally. Little variation in crystallinity occurs amongst the different phases. Number density of crystals, both 2D and 3D are 50-70 mm-2 and 30,000-50,000 mm-3 in the Plinian sample, compared to the lesser values in other eruptive types. Characteristic crystal size also increases as explosivity decreases. Two samples, both lava flows collected while warm, overlap with the Plinian sample. This suggests that the variations seen may be a result of cooling history. Plagioclase differs between the Plinian sample, in which they are only tabular in shape, and the other eruptive types, which contain both tabular and equant crystals. To link decompression paths of the Arenal magma to possible pre-eruptive conditions, we have carried out hydrothermal experiments. The experiments were preformed in TZM pressure vessels buffered at a fugacity of Ni-NiO and water saturation. Phase equilibria results in conjunction with mineral compositions and temperature estimates by previous workers from active lava flows and two-pyroxene geothermometry, constrain the likely pre-eruptive conditions for the Arenal magma to 950-1040° C with a water pressure of 50-80 MPa. Samples that started from conditions that bracket our estimated pre-eruptive conditions were decompressed in steps of 5-30 MPa and held for various times at each step until 20 MPa was reached, approximating average decompression rates of 0.25, 0.025, 0.0013 MPa/s. Comparison of textures found in the natural samples to the experimentally produced textures suggest that the Plinian eruption likely was fed by magma ascending at 0.05-1 m/s, whereas the less explosive phases were fed by magma ascending at 0.05 m/s or less.

Potential hydrothermal resource temperatures in the Eastern Snake River Plain, Idaho

Energy Technology Data Exchange (ETDEWEB)

Ghanashayam Neupane; Earl D. Mattson; Cody J. Cannon; Trevor A. Atkinson; Travis L. McLing; Thomas R. Wood; Patrick F. Dobson; Mark E. Conrad

2016-02-01

The Eastern Snake River Plain (ESRP) in southern Idaho is a region of high heat flow. Sustained volcanic activities in the wake of the passage of the Yellowstone Hotspot have turned this region into an area with great potential for geothermal resources as evidenced by numerous hot springs scattered along the margins of the plain and several hot-water producing wells and hot springs within the plain. Despite these thermal expressions, it is hypothesized that the pervasive presence of an overlying groundwater aquifer in the region effectively masks thermal signatures of deep-seated geothermal resources. The dilution of deeper thermal water and re-equilibration at lower temperature are significant challenges for the evaluation of potential resource areas in the ESRP. Over the past several years, we collected approximately 100 water samples from springs/wells for chemical analysis as well as assembled existing water chemistry data from literature. We applied several geothermometric and geochemical modeling tools to these chemical compositions of ESRP water samples. Geothermometric calculations based on principles of multicomponent equilibrium geothermometry with inverse geochemical modeling capability (e.g., Reservoir Temperature Estimator, RTEst) have been useful for the evaluation of reservoir temperatures. RTEst geothermometric calculations of ESRP thermal water samples indicated numerous potential geothermal areas with elevated reservoir temperatures. Specifically, areas around southern/southwestern side of the Bennett Hills and within the Camas Prairies in the western-northwestern regions of the ESRP and its margins suggest temperatures in the range of 140-200°C. In the northeastern portions of the ESRP, Lidy Hot Springs, Ashton, Newdale, and areas east of Idaho Falls have expected reservoir temperature =140 °C. In the southern ERSP, areas near Buhl and Twin Falls are found to have elevated temperatures as high as 160 °C. These areas are likely to host

Amphibole and felsic veins from the gabbroic oceanic core complex of Atlantis Bank (Southwest Indian Ridge, IODP Hole U1473A): when the fluids meets the melts

Science.gov (United States)

Sanfilippo, A.; Tribuzio, R.; Antonicelli, M.; Zanetti, A.

2017-12-01

We present a petrological/geochemical investigation of brown amphibole and felsic veins drilled during IODP 360 expedition at Atlantis Bank, a gabbroic oceanic core complex from Southwest Indian Ridge. The main purpose of this study is to unravel the role of seawater and magmatic components in the origin of these veins. Brown amphibole veins were collected at 90-170 mbsf. These veins typically include minor modal amounts of plagioclase and are associated with alteration halos made up of brown amphibole and whitish milky plagioclase in host gabbros. Two sets of late magmatic felsic veins, which mostly consist of plagioclase and minor brown amphibole, were selected. Amphibole-plagioclase geothermometry (Holland and Blundy, 1994) documents that crystallization of brown amphibole and felsic veins occurred in the 850-700 °C interval. In the brown amphibole veins, amphibole and plagioclase have relatively low concentrations of incompatible trace elements and significant Cl (0.2-0.3 wt%). The development of these veins at near surface levels is therefore attributed to seawater-derived fluids migrating downward through cracks developing in the exhuming gabbro. To explain the high temperature estimates for the development of these shallow veins, however, the seawater-derived fluids must have interacted not only with the gabbros, but also with a high temperature magmatic component. This petrogenetic hypothesis is consistent with oxygen and hydrogen isotopic compositions of amphiboles from shallow veins in adjacent Hole 735B gabbros (Alt and Bach, 2006). Trace element compositions of amphibole and plagioclase from the felsic veins show formation by silicate melts rich in incompatible elements. In addition, Cl concentrations in amphibole from the felsic veins are low, thereby indicating that the melts feeding these veins had low or no seawater component. We cautiously propose that: (i) the felsic veins were generated by SiO2-rich melts residual after crystallization of Fe

Dual stable isotopes of CH 4 from Yellowstone hot-springs suggest hydrothermal processes involving magmatic CO 2

Energy Technology Data Exchange (ETDEWEB)

Moran, James J.; Whitmore, Laura M.; Jay, Zackary J.; Jennings, Ryan deM.; Beam, Jacob P.; Kreuzer, Helen W.; Inskeep, William P.

2017-07-01

Volcanism and post-magmatism contribute both significant annual CH₄ fluxes to the atmosphere (on par with other natural sources such as forest fire and wild animal emissions) and have been implicated in past climate-change events. The Yellowstone hot spot is one of the largest volcanic systems on Earth and is known to emit methane in addition to other greenhouse gases (e.g. carbon dioxide) but the ultimate source of this methane flux has not been elucidated. Here we use dual stable isotope analysis (δ²H and δ¹³C) of CH₄(g) sampled from ten high-temperature geothermal pools in Yellowstone National Park to show that the predominant flux of CH4(g) is abiotic. The average δ¹³C and δ²H values of CH₄(g) emitted from hot springs (-26.7 (±2.4) and -236.9 (±12.0) ‰, respectively) are not consistent with biotic (microbial or thermogenic) methane sources, but are within previously reported ranges for abiotic methane production. Correlation between δ¹³C_CH4 and δ¹³C-dissolved inorganic C (DIC) also suggests that CO₂ is a parent C source for the observed CH₄(g). Moreover, CH₄-CO₂ isotopic geothermometry was used to estimate CH₄(g) formation temperatures ranging from ~ 250 - 350°C, which is just below the temperature estimated for the hydrothermal reservoir and consistent with the hypothesis that subsurface, rock-water interactions are responsible for large methane fluxes from this volcanic system. An understanding of conditions leading to the abiotic production of methane and associated isotopic signatures are central to understanding the evolutionary history of deep carbon sources on Earth.

Assessing Past Fracture Connectivity in Geothermal Reservoirs Using Clumped Isotopes: Proof of Concept in the Blue Mountain Geothermal Field, Nevada USA

Science.gov (United States)

Huntington, K. W.; Sumner, K. K.; Camp, E. R.; Cladouhos, T. T.; Uddenberg, M.; Swyer, M.; Garrison, G. H.

2015-12-01

geothermometry to assess fracture connectivity and geothermal reservoir characteristics in the past—with the potential to help optimize resource production and injection programs and better understand structural controls on mass and heat transfer in the subsurface.

Magmatic controls on eruption dynamics of the 1950 yr B.P. eruption of San Antonio Volcano, Tacaná Volcanic Complex, Mexico-Guatemala

Science.gov (United States)

Mora, Juan Carlos; Gardner, James Edward; Macías, José Luis; Meriggi, Lorenzo; Santo, Alba Patrizia

2013-07-01

San Antonio Volcano, in the Tacaná Volcanic Complex, erupted ~ 1950 yr. B.P., with a Pelean type eruption that produced andesitic pyroclastic surges and block-and-ash flows destroying part of the volcano summit and producing a horse-shoe shaped crater open to the SW. Between 1950 and 800 yr B.P. the eruption continued with effusive andesites followed by a dacite lava flow and a summit dome, all from a single magma batch. All products consist of phenocrysts and microphenocrysts of zoned plagioclase, amphibole, pyroxene, magnetite ± ilmenite, set in partially crystallized groundmass of glass and microlites of the same mineral phases, except for the lack of amphibole. Included in the andesitic blocks of the block-and-ash flow deposit are basaltic andesite enclaves with elongated and ellipsoidal forms and chilled margins. The enclaves have intersertal textures with brown glass between microphenocrysts of plagioclase, hornblende, pyroxene, and olivine, and minor proportions of phenocrysts of plagioclase, hornblende, and pyroxene. A compositional range obtained of blocks and enclaves resulted from mixing between andesite (866 °C ± 22) and basaltic andesite (enclaves, 932 °C ± 22), which may have triggered the explosive Pelean eruption. Vestiges of that mixing are preserved as complex compositional zones in plagioclase and clinopyroxene-rich reaction rims in amphibole in the andesite. Whole-rock chemistry, geothermometry, experimental petrology and modeling results suggest that after the mixing event the eruption tapped hybrid andesitic magma (≤ 900 °C) and ended with effusive dacitic magma (~ 825 °C), all of which were stored at ~ 200 MPa water pressure. A complex open-system evolution that involved crustal end-members best explains the generation of effusive dacite from the hybrid andesite. Amphibole in the dacite is rimmed by reaction products of plagioclase, orthopyroxene, and Fe-Ti oxides produced by decompression during ascent. Amphibole in the andesite

Resetting of Mg isotopes between calcite and dolomite during burial metamorphism: Outlook of Mg isotopes as geothermometer and seawater proxy

Science.gov (United States)

Hu, Zhongya; Hu, Wenxuan; Wang, Xiaomin; Lu, Yizhou; Wang, Lichao; Liao, Zhiwei; Li, Weiqiang

2017-07-01

Magnesium isotopes are an emerging tool to study the geological processes recorded in carbonates. Calcite, due to its ubiquitous occurrence and the large Mg isotope fractionation associated with the mineral, has attracted great interests in applications of Mg isotope geochemistry. However, the fidelity of Mg isotopes in geological records of carbonate minerals (e.g., calcite and dolomite) against burial metamorphism remains poorly constrained. Here we report our investigation on the Mg isotope systematics of a dolomitized Middle Triassic Geshan carbonate section in eastern China. Magnesium isotope analysis was complemented by analyses of Sr-C-O isotopic compositions, major and trace element concentrations, and petrographic and mineralogical features. Multiple lines of evidence consistently indicated that post-depositional diagenesis of carbonate minerals occurred to the carbonate rocks. Magnesium isotope compositions of the carbonate rocks closely follow a mixing trend between a high δ26Mg dolomite end member and a low δ26Mg calcite end member, irrespective of sample positions in the section and calcite/dolomite ratio in the samples. By fitting the measured Mg isotope data using a two-end member mixing model, an inter-mineral Δ26Mgdolomite-calcite fractionation of 0.72‰ was obtained. Based on the experimentally derived Mg isotope fractionation factors for dolomite and calcite, a temperature of 150-190 °C was calculated to correspond to the 0.72‰ Δ26Mgdolomite-calcite fractionation. Such temperature range matches with the burial-thermal history of the local strata, making a successful case of Mg isotope geothermometry. Our results indicate that both calcite and dolomite had been re-equilibrated during burial metamorphism, and based on isotope mass balance of Mg, the system was buffered by dolomite in the section. Therefore, burial metamorphism may reset Mg isotope signature of calcite, and Mg isotope compositions in calcite should be dealt with caution in

An experimental investigation of Na incorporation in cordierite in low P/high T metapelites

Science.gov (United States)

Tropper, Peter; Wyhlidal, Stefan; Haefeker, Udo A.; Mirwald, Peter W.

2018-04-01

contents could reflect this disequilibrium behaviour. Preliminary geothermometric calculations using the data from the W experiments are in very good agreement with T estimates from conventional geothermometry in metapelitic contact aureoles as well as high-grade migmatic gneisses from the literature.

Long term storage of explosively erupted magma at Nevado de Toluca volcano, Mexico

Science.gov (United States)

Arce, J. L.; Gardner, J.; Macias, J. L.

2007-12-01

Dacitic magmas production is common in subduction-related volcanoes, occurring in those with a long period of activity as a result of the magmatic evolution. However, in this evolution many factors (i.e. crystal fractionation, assimilation, magma mixing) can interact to produce dacites. Nevado de Toluca volcano (4,680 masl; 19°09'N; 99°45'W) Central Mexico has recorded a long period of time producing dacites explosively, at least during 42 ka of activity, involving several km3 of magma, with two important Plinian-type eruptions occurred at ~21.7 ka (Lower Toluca Pumice) and ~10.5 ka (Upper Toluca Pumice). Questions like, what was the mechanism responsible to produce voluminous dacitic magma and how the volatiles and pressure changed in the Nevado de Toluca system, remain without answers. Dacites from the Lower Toluca Pumice (LTP) contain plagioclase, amphibole, iron-titanium oxides, and minor resorbed biotite, set in a glassy-vesicular matrix and the Upper Toluca Pumice (UTP) dacites contain the same mineral phases plus orthopyroxene. Ilmenite- ulvospinel geothermometry yielded a temperature of ~860°C for the LTP dacite, a little hotter than the UTP (~ 840°C). Based on hydrothermal experiments data, amphibole is stable above 100 MPa under 900°C, while plagioclase crystallizes up to 250-100 MPa at temperatures of 850-900°C. Pyroxene occurs only at pressures of 200-100 MPa with its respective temperatures of 825-900°C. Water contents in the LTP magma (2-3.5 wt %) are similar to that calculated for the UTP magma (1.3-3.6 wt %). So, there are only small changes in temperature and pressure from ~21.7 ka to 10.5 ka. It is noteworthy that orthopyroxene is absent in the LTP, however reaction-rimmed biotite (probably xenocrystic) is commonly observed in all dacites. Hence, almost all dacitic magmas seem to be stored at relatively similar pressures, water contents, and temperatures. All of these data could suggest repetitive basic magma injections producing the

Thermal springs, fumaroles and gas vents of continental Yemen: Their relation with active tectonics, regional hydrology and the country's geothermal potential

International Nuclear Information System (INIS)

Minissale, Angelo; Mattash, Mohamed A.; Vaselli, Orlando; Tassi, Franco; Al-Ganad, Ismail N.; Selmo, Enrico; Shawki, Nasr M.; Tedesco, Dario; Poreda, Robert; Ad-Dukhain, Abdassalam M.; Hazzae, Mohammad K.

2007-01-01

Most thermal springs of continental Yemen (about 65 emergences at 48 sampling sites) and a couple of fumaroles and boiling water pools have been sampled and analyzed for chemical and isotopic composition in the liquid phase and the associated free-gas phase. Whatever the emergence, all the water discharges have an isotopic signature of meteoric origin. Springs seeping out from high altitudes in the central volcanic plateau show a prevalent Na-HCO 3 -composition, clearly affected by an anomalous flux of deep CO 2 deriving from active hydrothermal systems located in the Jurassic Amran Group limestone sequence and/or the Cretaceous Tawilah Group, likely underlying the 2000-3000 m thick volcanic suite. At lower elevations, CO 2 also affects the composition of some springs emerging at the borders of the central volcanic plateau. Although mixing to a limited extent with organic CO 2 infiltrating together with the meteoric recharge waters cannot be ruled out, all the CO 2 -rich gas samples have a δ 13 C-CO 2 signature that falls in the range of mantle CO 2 (-3 13 C 3 He/ 4 He (1 a 2 -rich springs and also some mixed N 2 -CO 2 gas vents in the far east Hadramaut region support the presence of mantle magmas and related hydrothermal systems residing at the crust level in several areas of Yemen. This well agrees with the presence of Quaternary basaltic magmatic activity along the Gulf of Aden, as well as inside the central Yemen volcanic plateau. Presently, the thermal springs of Yemen are prevalently used for spas and/or bathing. Nevertheless, liquid- and gas-geothermometry and geological considerations suggest that there are at least three areas (Al Lisi, Al Makhaya and Damt) inside the Yemen volcanic plateau (around Dhamar) that may be promising prospects for the future development of geothermal energy in Yemen. Alternatively, they could be used as a source of energy for small-to-medium scale agriculture and/or industrial purposes. Moreover, most of the thermal water

A geothermal resource in the Puna plateau (Jujuy Province, Argentina): New insights from the geochemistry of thermal fluid discharges

Science.gov (United States)

Peralta Arnold, Yesica; Cabassi, Jacopo; Tassi, Franco; Caffe, Pablo; Vaselli, Orlando

2017-04-01

Several hydrothermal mineralization and thermal fluid discharges are distributed in the high altitude Puna plateau at the eastern border of the Central Volcanic Zone of the Andes in the Jujuy Province, a region where volcanic explosive activity developed from Oligocene-Miocene to Neogene produced giant calderas and huge ignimbrite deposits. This study presents the geochemical and isotopic composition of thermal fluids discharged from Granada, Vilama, Pairique, Coranzulì and Olaroz zones, which are located between S 22°20'- 23°20' and W 66°- 67°. This aim is to provide insights into the physicochemical features of the deep fluid circulating system in order to have a preliminary indication about the geothermal potential in this area. The occurrence of partially mature Na+-Cl- waters suggests that a deep (>5,000 m b.g.l.) hydrothermal reservoir, hosted within the Paleozoic crystalline basement, represents the main fluid source. Regional tectonics, dominated by S-oriented faulting systems that produced a horst and graben tectonics, as well as NE-, NW- and WE-oriented transverse structures, favour the uprising of the deep-originated fluids, including a significant amount (up to 16%) of mantle He. The dry gas phase mainly consists of CO2 mostly produced from subducted C-bearing organic-rich material. The interaction between meteoric water and Cretaceous, Palaeogene to Miocene sediments at shallow depth gives rise to relatively cold Na+-HCO3-type aquifers. Dissolution of evaporitic surficial deposits (salares), produced by the arid climate of the region, strongly affects the chemistry of the thermal springs in the peripheral zones of the study area. Geothermometry in the Na-K-Ca-Mg system suggests equilibrium temperatures up to 200 °C for the deep aquifer, whereas the H2 geothermometer equilibrates at lower temperatures (from 105 to 155 °C), likely corresponding to those of the shallower aquifer. Although the great depth of the main fluid reservoir represents a

Genesis of the Abu Marawat gold deposit, central Eastern Desert of Egypt

Science.gov (United States)

Zoheir, Basem A.; Akawy, Ahmed

2010-06-01

-in-chlorite geothermometry of chlorite associated with sulphides in the mineralised quartz veins. Fracturing enhanced fluid circulation through the wallrock and related BIF, allowing reaction of the S-bearing ore fluid with iron oxides. This caused pyrite formation and concomitant Au precipitation, enhanced by fluid immiscibility as H 2S partitioned preferentially into the carbonic phase. The ore fluids may have originated from granitoid intrusions (likely the post-Hammamat felsites, whereas gold and base metals might have been leached from the Abu Marawat basic metavolcanics.

Lithospheric strength in the active boundary between the Pacific Plate and Baja California microplate constrained from lower crustal and upper mantle xenoliths

Science.gov (United States)

Chatzaras, Vasileios; van der Werf, Thomas; Kriegsman, Leo M.; Kronenberg, Andreas; Tikoff, Basil; Drury, Martyn R.

2017-04-01

The lower crust is the most poorly understood of the lithospheric layers in terms of its rheology, particularly at active plate boundaries. We studied naturally deformed lower crustal xenoliths within an active plate boundary, in order to link their microstructures and rheological parameters to the well-defined active tectonic context. The Baja California shear zone (BCSZ), located at the western boundary of the Baja California microplate, comprises the active boundary accommodating the relative motion between the Pacific plate and Baja California microplate. The basalts of the Holocene San Quintin volcanic field carry lower crustal and upper mantle xenoliths, which sample the Baja California microplate lithosphere in the vicinity of the BCSZ. The lower crustal xenoliths range from undeformed gabbros to granoblastic two-pyroxene granulites. Two-pyroxene geothermometry shows that the granulites equilibrated at temperatures of 690-920 oC. Phase equilibria (P-T pseudosections using Perple_X) indicate that symplectites with intergrown pyroxenes, plagioclase, olivine and spinel formed at 3.6-5.4 kbar, following decompression from pressures exceeding 6 kbar. FTIR spectroscopy shows that the water content of plagioclase varies among the analyzed xenoliths; plagioclase is relatively dry in two xenoliths while one xenolith contains hydrated plagioclase grains. Microstructural observations and analysis of the crystallographic texture provide evidence for deformation of plagioclase by a combination of dislocation creep and grain boundary sliding. To constrain the strength of the lower crust and upper mantle near the BCSZ we estimated the differential stress using plagioclase and olivine grain size paleopiezomtery, respectively. Differential stress estimates for plagioclase range from 10 to 32 MPa and for olivine are 30 MPa. Thus the active microplate boundary records elevated crustal temperatures, heterogeneous levels of hydration, and low strength in both the lower crust and

The Hydrogeochemistry of Qingshui Geothermal Field, Northeastern Taiwan.

Science.gov (United States)

Yu-Wen, Chen; Cheng-Kuo, Lin; Wayne, Lin; Yu-Te, Chang; Pei-Shan, Hsieh

2015-04-01

The Qingshui geothermal field is located at the upstream valley of Lanyang Creek, northeastern Taiwan. It is renowned as a geothermal field. The previous studies demonstrated a higher geothermal gradient, 100oC/km warmer than a normal geotherm. However, Qingshui geothermal field has not been well developed due to the higher mining costs. In the recent years, the Taiwan government has been focusing on developing alternative and renewable energy and initiated a 10 year project, Nation Energy Program. This study is part of this project In general, it is very difficult to collect deep downhole samples without considerable change of hydro- and gas- chemistry of water under high temperature and pressure. A new sampling tool, GTF Sampler, was designed by the research team, Green Energy and Environment Laboratories, Industrial Technology Research Institute. This tool can simultaneously collect high quality geothermal water and gas sample and moreover, the sampling depth can reach up to 800 meters. Accordingly, a more accurate measurements can be conducted in the laboratory. In this study, 10 geothermal samples were collected and measured. The results demonstrate that geothermal water samples are characterized with Na(K)-HCO3 water type and located at the mature water area in Giggenbach Na-K-Mg diagram. Several geothermometers, including silica and cation geothermometry, were used to estimate potential temperature in the geothermal reservoir systems. In general, the geothermoters of Na-K and Na-K-Ca obtain reservoir temperatures between 120-190oC and 130-210oC, respectively, but the silica geothermometer indicates a lower reservoir temperature between 90 and 170oC. There is no big difference among them. It is worth to note that all calculated temperatures are lower than those of in-situ downhole measurements; therefore, more detailed and advanced researches would be needed for the inconsistency. To examine the argument about igneous heat source in the previous studies, rare

Explosive to Effusive Transition in Intermediate Volcanism: An Analysis of Changing Magma System Conditions in Dominica

Science.gov (United States)

Bersson, J.; Waters, L. E.; Frey, H. M.; Nicolaysen, K. P.; Manon, M. R. F.

2017-12-01

The oscillation between explosive and effusive intermediate (59-62 wt% SiO2) volcanism in the Roseau Valley on Dominica, an island in the Lesser Antilles Arc, provides an opportunity to investigate temporal changes in the magmatic system. Here, we test the relationship between the Roseau ignimbrites (1-65 ka) and the Micotrin dome ( 1.1 ka) which are proposed to originate from the same magmatic system, with a detailed petrologic analysis of phenocrysts to determine commonalities or changes in pre-eruptive conditions (i.e., intensive variables). The ignimbrites are saturated in five phenocrysts (plagioclase + orthopyroxene + clinopyroxene + ilmenite + magnetite ± amphibole ± quartz), and the lava dome contains the same assemblage, but with notable differences: amphiboles are entirely reacted, and quartz occurs in greater abundance. Plagioclase in the ignimbrites ranges in composition from An46-93, and those in the dome range from An46-85. Two Fe-Ti oxide geo-thermometry reveal pre-eruptive temperatures from 730-820°C for three different ignimbrite units, whereas the pre-eruptive temperature for the dome is slightly hotter (850±23°C). Values of fO2 (relative to NNO) derived from Fe-Ti oxide oxygen-barometry range from +0.3 to +1.32 ΔNNO for the ignimbrites, which overlap with those from the dome (+0.5 to +0.9 ΔNNO). Pre-eruptive temperatures, plagioclase compositions, whole rock and glass compositions are incorporated into a plagioclase-liquid hygrometer to determine pre-eruptive melt H2O contents for each sample. H2O contents for ignimbrites range from 7.1-9.3 wt%, and those from the lava dome range from 6.7-7.1 wt%. Application of a H2O solubility model shows that water contents for the Roseau magmas correspond to pressures of 3-5 kbar. The most notable difference between the explosive and effusive magmas is that the lava dome has a higher pre-eruptive temperature than the ignimbrites. However, the results collectively suggest that more recent volcanism in

A geochemical approach for assessing the possible uses of the geothermal resource in the eastern sector of the Sabatini Volcanic District (Central Italy)

Science.gov (United States)

Cinti, Daniele; Tassi, Franco; Procesi, Monia; Brusca, Lorenzo; Cabassi, Jacopo; Capecchiacci, Francesco; Delgado Huertas, Antonio; Galli, Gianfranco; Grassa, Fausto; Vaselli, Orlando; Voltattorni, Nunzia

2017-04-01

, permeate. Accordingly, gas geothermometry in the CH4-CO2-H2 and H2S-CO2-H2 systems suggests equilibrium temperatures <200 °C, i.e. significantly lower than those measured in fluids from deep geothermal wells (300 °C). Although mitigated by the short distance from the Apennine range, the thermal anomaly recognized by fluid geochemistry in the eastern SVD makes this area suitable for direct exploitation of the geothermal resource.

Thermal springs, fumaroles and gas vents of continental Yemen: Their relation with active tectonics, regional hydrology and the country's geothermal potential

Energy Technology Data Exchange (ETDEWEB)

Minissale, Angelo [CNR - Italian Council for Research, Institute of Geosciences and Earth Resources of Florence, Via La Pira 4, 50121 Florence (Italy)]. E-mail: minissa@igg.cnr.it; Mattash, Mohamed A. [Ministry of Oil and Mineral Resources, Geological Survey and Minerals Resources Board, P.O. Box 297, Sana' a (Yemen); Vaselli, Orlando [Department of Earth Sciences, Via La Pira 4, 50121 Firenze (Italy); CNR - Italian Council for Research, Institute of Geosciences and Earth Resources of Florence, Via La Pira 4, 50121 Firenze (Italy); Tassi, Franco [Department of Earth Sciences, Via La Pira 4, 50121 Firenze (Italy); Al-Ganad, Ismail N. [Ministry of Oil and Mineral Resources, Geological Survey and Minerals Resources Board, P.O. Box 297, Sana' a (Yemen); Selmo, Enrico [Department of Earth Sciences, Parco Area delle Scienze 157A, 43100 Parma (Italy); Shawki, Nasr M. [Department of Geology, University of Ta' iz, P.O. Box 5679, Ta' iz (Yemen); Tedesco, Dario [Department of Environmental Sciences, Second University of Naples, Via Vivaldi 43, 81100 Caserta (Italy); Poreda, Robert [Department of Earth and Environmental Sciences, 227 Hutchinson Hall, Rochester, NY 14627 (United States); Ad-Dukhain, Abdassalam M. [Ministry of Oil and Mineral Resources, Geological Survey and Minerals Resources Board, P.O. Box 297, Sana' a (Yemen); Hazzae, Mohammad K. [Ministry of Oil and Mineral Resources, Geological Survey and Minerals Resources Board, P.O. Box 297, Sana' a (Yemen)

2007-04-15

Most thermal springs of continental Yemen (about 65 emergences at 48 sampling sites) and a couple of fumaroles and boiling water pools have been sampled and analyzed for chemical and isotopic composition in the liquid phase and the associated free-gas phase. Whatever the emergence, all the water discharges have an isotopic signature of meteoric origin. Springs seeping out from high altitudes in the central volcanic plateau show a prevalent Na-HCO{sub 3}-composition, clearly affected by an anomalous flux of deep CO{sub 2} deriving from active hydrothermal systems located in the Jurassic Amran Group limestone sequence and/or the Cretaceous Tawilah Group, likely underlying the 2000-3000 m thick volcanic suite. At lower elevations, CO{sub 2} also affects the composition of some springs emerging at the borders of the central volcanic plateau. Although mixing to a limited extent with organic CO{sub 2} infiltrating together with the meteoric recharge waters cannot be ruled out, all the CO{sub 2}-rich gas samples have a {delta} {sup 13}C-CO{sub 2} signature that falls in the range of mantle CO{sub 2} (-3 < {delta} {sup 13}C < -7 per mille V-PDB). The relatively high {sup 3}He/{sup 4}He (1 < R/R {sub a} < 3.2) ratios measured in all the CO{sub 2}-rich springs and also some mixed N{sub 2}-CO{sub 2} gas vents in the far east Hadramaut region support the presence of mantle magmas and related hydrothermal systems residing at the crust level in several areas of Yemen. This well agrees with the presence of Quaternary basaltic magmatic activity along the Gulf of Aden, as well as inside the central Yemen volcanic plateau. Presently, the thermal springs of Yemen are prevalently used for spas and/or bathing. Nevertheless, liquid- and gas-geothermometry and geological considerations suggest that there are at least three areas (Al Lisi, Al Makhaya and Damt) inside the Yemen volcanic plateau (around Dhamar) that may be promising prospects for the future development of geothermal energy

Constraints on the rheology of the lower crust in a strike-slip plate boundary: evidence from the San Quintín xenoliths, Baja California, Mexico

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T. van der Werf

2017-12-01

Full Text Available The rheology of lower crust and its transient behavior in active strike-slip plate boundaries remain poorly understood. To address this issue, we analyzed a suite of granulite and lherzolite xenoliths from the upper Pleistocene–Holocene San Quintín volcanic field of northern Baja California, Mexico. The San Quintín volcanic field is located 20 km east of the Baja California shear zone, which accommodates the relative movement between the Pacific plate and Baja California microplate. The development of a strong foliation in both the mafic granulites and lherzolites, suggests that a lithospheric-scale shear zone exists beneath the San Quintín volcanic field. Combining microstructural observations, geothermometry, and phase equilibria modeling, we estimated that crystal-plastic deformation took place at temperatures of 750–890 °C and pressures of 400–560 MPa, corresponding to 15–22 km depth. A hot crustal geotherm of 40 ° C km−1 is required to explain the estimated deformation conditions. Infrared spectroscopy shows that plagioclase in the mafic granulites is relatively dry. Microstructures are interpreted to show that deformation in both the uppermost lower crust and upper mantle was accommodated by a combination of dislocation creep and grain-size-sensitive creep. Recrystallized grain size paleopiezometry yields low differential stresses of 12–33 and 17 MPa for plagioclase and olivine, respectively. The lower range of stresses (12–17 MPa in the mafic granulite and lherzolite xenoliths is interpreted to be associated with transient deformation under decreasing stress conditions, following an event of stress increase. Using flow laws for dry plagioclase, we estimated a low viscosity of 1.1–1.3×1020 Pa ⋅ s for the high temperature conditions (890 °C in the lower crust. Significantly lower viscosities in the range of 1016–1019 Pa ⋅ s, were estimated using flow laws for wet plagioclase. The

Constraints on the rheology of the lower crust in a strike-slip plate boundary: evidence from the San Quintín xenoliths, Baja California, Mexico

Science.gov (United States)

van der Werf, Thomas; Chatzaras, Vasileios; Marcel Kriegsman, Leo; Kronenberg, Andreas; Tikoff, Basil; Drury, Martyn R.

2017-12-01

The rheology of lower crust and its transient behavior in active strike-slip plate boundaries remain poorly understood. To address this issue, we analyzed a suite of granulite and lherzolite xenoliths from the upper Pleistocene-Holocene San Quintín volcanic field of northern Baja California, Mexico. The San Quintín volcanic field is located 20 km east of the Baja California shear zone, which accommodates the relative movement between the Pacific plate and Baja California microplate. The development of a strong foliation in both the mafic granulites and lherzolites, suggests that a lithospheric-scale shear zone exists beneath the San Quintín volcanic field. Combining microstructural observations, geothermometry, and phase equilibria modeling, we estimated that crystal-plastic deformation took place at temperatures of 750-890 °C and pressures of 400-560 MPa, corresponding to 15-22 km depth. A hot crustal geotherm of 40 ° C km-1 is required to explain the estimated deformation conditions. Infrared spectroscopy shows that plagioclase in the mafic granulites is relatively dry. Microstructures are interpreted to show that deformation in both the uppermost lower crust and upper mantle was accommodated by a combination of dislocation creep and grain-size-sensitive creep. Recrystallized grain size paleopiezometry yields low differential stresses of 12-33 and 17 MPa for plagioclase and olivine, respectively. The lower range of stresses (12-17 MPa) in the mafic granulite and lherzolite xenoliths is interpreted to be associated with transient deformation under decreasing stress conditions, following an event of stress increase. Using flow laws for dry plagioclase, we estimated a low viscosity of 1.1-1.3×1020 Pa ṡ s for the high temperature conditions (890 °C) in the lower crust. Significantly lower viscosities in the range of 1016-1019 Pa ṡ s, were estimated using flow laws for wet plagioclase. The shallow upper mantle has a low viscosity of 5.7×1019 Pa ṡ s

Alaska Open-File Report 127 Assessment of Thermal Springs Sites in Southern Southeastern Alaska - Preliminary Results and Evaluation

Energy Technology Data Exchange (ETDEWEB)

Motyka, Roman J.; Moorman, Mary A.; Reeder, John W.

1980-06-01

Information has been gathered on 13 reported thermal-spring sites, 12 in southern Southeastern Alaska and one in western British Columbia. Five of the reported sites could not be substantiated by DGGS. The eight known thermal spring sites are associated with grainitic terrain and, except for Baker Island Hot Springs, occur within or near intensively fractured Cretaceous-age pluons of the Coast Range Batholith. Thermal-spring surface temperatures range from 21 C (Twin Lakes) to 91.5 C (Bailey Bay). The greatest discharge occurs at Chief Shakes hot springs (450 1pm). Bell Island Hot Springs, which has about a 100-1 pm discharge and a 70 C temperature, has had the most development. Two previously unreported thermal-spring sites, Barnes Lake warm springs and Bradfield hot springs, have a low rate of discharge and respective surface temperatures of about 25 and 54 C. The known thermal springs probably originate from circulation of meteoric waters through deep-seated fracture and fault systems. The chemical constituents of the alkali-sulfate to alkali-chloride thermal waters are probably derived from interaction of the deeply circulating meteoric waters with the granitic wall rocks. Chemical geothermometry suggests subsurface temperatures of 55 to 151 C. If waters are being heated solely by conduction from wall rocks, circulation depths must be about 1.5 to 5 km, assuming geothermal gradients of 30 to 50 C/km. Variations in temperature, discharge, and chemistry were noted at several thermal springs for which previous records are available. A major decrease in silica and potassium concentrations at Chief Shakes hot springs is suggested by comparing recent analyses of water chemistry to Waring's (1917) original analysis. The rate of discharge at Bell Island Hot Springs may have increased by a factor of two since Waring's visit to the springs. Subsurface reservoirs associated with thermal springs in southern Southeastern Alaska are of low temperature and are

Development of Genetic Occurrence Models for Geothermal Prospecting

Science.gov (United States)

Walker, J. D.; Sabin, A.; Unruh, J.; Monastero, F. C.; Combs, J.

2007-12-01

, including high heat flow, anomalous temperature water wells, high-temperature indications from aqueous geothermometry and geochemistry, Pliocene or younger ages from low-temperature thermochronometers, as well as more obvious factors such as geysers and fumaroles (which by definition will be missing for blind resources). Our occurrence-model strategy inverts the current approach that relies first on obvious evidence of geothermal activity. We evaluated our approach by retrospectively applying the protocol to the characteristics of producing geothermal fields, and in all cases, known resource areas fit the parameters identified from a genetic perspective.

Chemical and isotopic characteristics of geothermal fluids from Sulphur Springs, Saint Lucia

Science.gov (United States)

Joseph, Erouscilla P.; Fournier, Nicolas; Lindsay, Jan M.; Robertson, Richard; Beckles, Denise M.

2013-03-01

Sulphur Springs is a vigorous, geothermal field associated with the active Soufrière Volcanic Centre in southern Saint Lucia, Lesser Antilles island arc. The 'Sulphur Springs Park' is an important tourist attraction (touted as the 'world's only drive-through volcano') with some of the hot pools being developed into recreational pools. Some 200,000 people visit the park each year. Since 2001, the hydrothermal fluids of Sulphur Springs have been sampled as part of an integrated volcanic monitoring programme for the island. Gas and water samples were analysed to characterise the geochemistry of the hydrothermal system, and to assess the equilibrium state and subsurface temperatures of the reservoir. This has also enabled us, for the first time, to establish baseline data for future geochemical monitoring. The gases are of typical arc-type composition, with N2 excess and low He and Ar content. The dry gas composition is dominated by CO2 (ranging from 601-993 mmol/mol), with deeper magmatic sourced H2S-rich vapour undergoing boiling and redox changes in the geothermal reservoir to emerge with a hydrothermal signature in the fumarolic gases. Fluid contributions from magmatic degassing are also evident, mainly from the moderate to high contents of HCl and deeply-sourced H2S gas, respectively. Sulphur Springs hydrothermal waters have acid-sulphate type compositions (SO4 = 78-4008 mg/L; pH = 3-7), and are of primarily meteoric origin which have been affected by evaporation processes based on the enrichment in both δ18O and δD (δ18O = - 1 to 15‰ and δD = - 9 to 14‰ respectively) in relation to the global meteoric water line (GMWL). These waters are steam-heated water typically formed by absorption of H2S-rich gases in the near surface oxygenated groundwaters. Reservoir temperatures calculated from the evaluation of gas equilibria in the CO2-CH4-H2 system reveal higher temperatures (190 to 300 °C) than those derived from quartz geothermometry (95 to 169 °C), which

Groundwater evolution in the Continental Intercalaire aquifer of southern Algeria and Tunisia: trace element and isotopic indicators

International Nuclear Information System (INIS)

Edmunds, W.M.; Guendouz, A.H.; Mamou, A.; Moulla, A.; Shand, P.; Zouari, K.

2003-01-01

The geochemical processes taking place along an 800 km flow line in the non-carbonate Continental Intercalaire aquifer (CI) aquifer in North Africa are described using chemical (major and trace element) and isotopic indicators. The aquifer is hydraulically continuous from the Atlas Mountains in Algeria to the Chotts of Tunisia and the geochemical evidence corroborates this. The highest discharge temperature is 73 deg. C but silica geothermometry indicates a maximum temperature of 94 deg. C at depth. Chloride concentrations increase from 200 to 800 mg l -1 and the Br/Cl ratios confirm the dissolution of non-marine evaporites or interstitial waters as the main source of salinity. Fluoride concentrations are low and are likely to be derived from rainfall, recording oscillations in source. Radiocarbon ages, except near outcrop, are at or near detection limits and the δ 18 O and δ 2 H values indicate a cooler recharge regime with rainfall having lower primary evaporation than today. This is shown by the fact that mean isotope ratios of CI waters are around 3 per mille lighter than the present-day weighted mean value for rain. Major ion ratios and most trace elements indicate that despite the complex structure and stratigraphy, uniform evolution with continuous water-rock interaction takes place along the flow lines, which are only disturbed near the Tunisian Chotts by groundwater converging from additional flow lines. The ageing of the water can also be followed by the smooth increase in several indicator elements such as Li, K and Mn which are least affected by solubility controls. Similarly the influence of marine facies in the Tunisian sector may be recognised by the changing Mg/Ca and higher Br/Cl as well as trace element indicators. The groundwaters are oxidising up to 300 km from outcrop (dissolved O 2 has persisted for at least 20 ka) and within this zone the concentrations of several elements forming oxy-anions, such as U and Cr, increase and NO 3 remains

Infrared Spectroscopy for Rapid Characterization of Drill Core and Cutting Mineralogy

Science.gov (United States)

Calvin, W. M.; Kratt, C.; Kruse, F. A.

2009-12-01

and hydroxides in geothermal drill samples. We are currently developing automated analysis techniques to convert this detailed spectral logging data into high-vertical-resolution mineral depth profiles that can be linked to lithology, stratigraphy, fracture zones and potential for geothermal production. Also in development are metrics that would link mapped mineralogy to known geothermometers such as Na-K, Mg depletion, discrimination among illite, montmorillonite, and beidellite, and kaolinite crystallinity. Identification of amorphous and crystalline silica components (chalcedony, crystobalite and quartz) can also constrain silica geothermometry. The degree of alteration and some mineral types have been shown to be a proxy for host rock permeability, natural circulation, and the potential for reservoir sealing. Analysis of alteration intensity is also under way. We will present a synthesis of results to date.

Sulfur isotope study of the Velardeña skarn (Zn-Pb), Durango, Mexico

Science.gov (United States)

Jimenez, A.

2012-04-01

outside the common range of magmatic sulfur; it corresponds to a sphalerite crystal with δ34S of -3.9 ‰. This negative value could be explained by the incorporation of sulfur leached from the sedimentary host rocks. Pyrite and galena in paragenesis were analyzed from one sample (CO-9F); the isotope fractionation equation of Ohmoto and Rye (1979) was applied for geothermometry purposes. This calculation yields a temperature of 346° ±25° C, from fractionation Δpyrite-galena of 2.66 ‰.

Mixing effects on geothermometric calculations of the Newdale geothermal area in the Eastern Snake River Plain, Idaho

Energy Technology Data Exchange (ETDEWEB)

Ghanashayam Neupane; Earl D. Mattson; Travis L. McLing; Cody J. Cannon; Thomas R. Wood; Trevor A. Atkinson; Patrick F. Dobson; Mark E. Conrad

2016-02-01

The Newdale geothermal area in Madison and Fremont Counties in Idaho is a known geothermal resource area whose thermal anomaly is expressed by high thermal gradients and numerous wells producing warm water (up to 51 °C). Geologically, the Newdale geothermal area is located within the Eastern Snake River Plain (ESRP) that has a time-transgressive history of sustained volcanic activities associated with the passage of Yellowstone Hotspot from the southwestern part of Idaho to its current position underneath Yellowstone National Park in Wyoming. Locally, the Newdale geothermal area is located within an area that was subjected to several overlapping and nested caldera complexes. The Tertiary caldera forming volcanic activities and associated rocks have been buried underneath Quaternary flood basalts and felsic volcanic rocks. Two southeast dipping young faults (Teton dam fault and an unnamed fault) in the area provide the structural control for this localized thermal anomaly zone. Geochemically, water samples from numerous wells in the area can be divided into two broad groups – Na-HCO3 and Ca-(Mg)-HCO3 type waters and are considered to be the product of water-rhyolite and water-basalt interactions, respectively. Each type of water can further be subdivided into two groups depending on their degree of mixing with other water types or interaction with other rocks. For example, some bivariate plots indicate that some Ca-(Mg)-HCO3 water samples have interacted only with basalts whereas some samples of this water type also show limited interaction with rhyolite or mixing with Na-HCO3 type water. Traditional geothermometers [e.g., silica variants, Na-K-Ca (Mg-corrected)] indicate lower temperatures for this area; however, a traditional silica-enthalpy mixing model results in higher reservoir temperatures. We applied a new multicomponent equilibrium geothermometry tool (e.g., Reservoir Temperature Estimator, RTEst) that is based on inverse geochemical modeling which

Geochemical exploration of a promissory Enhanced Geothermal System (EGS): the Acoculco caldera, Mexico.

Science.gov (United States)

Peiffer, Loic; Romero, Ruben Bernard; Pérez-Zarate, Daniel; Guevara, Mirna; Santoyo Gutiérrez, Edgar

2014-05-01

The Acoculco caldera (Puebla, Mexico) has been identified by the Mexican Federal Electricity Company (in Spanish 'Comisión Federal de Electricidad', CFE) as a potential Enhanced Geothermal System (EGS) candidate. Two exploration wells were drilled and promising temperatures of ~300° C have been measured at a depth of 2000 m with a geothermal gradient of 11oC/100m, which is three times higher than the baseline gradient measured within the Trans-Mexican Volcanic Belt. As usually observed in Hot Dry Rock systems, thermal manifestations in surface are scarce and consist in low-temperature bubbling springs and soil degassing. The goals of this study were to identify the origin of these fluids, to estimate the soil degassing rate and to explore new areas for a future detailed exploration and drilling activities. Water and gas samples were collected for chemical and isotopic analysis (δ18O, δD, 3He/4He, 13C, 15N) and a multi-gas (CO2, CH4, H2S) soil survey was carried out using the accumulation chamber method. Springs' compositions indicate a meteoric origin and the dissolution of CO2 and H2S-rich gases, while gas compositions reveal a MORB-type origin mixed with some arc-type contribution. Gas geothermometry results are similar to temperatures measured during well drilling (260° C-300° C). Amongst all measured CO2 fluxes, only 5% (mean: 5543 g m-2 day-1) show typical geothermal values, while the remaining fluxes are low and correspond to biogenic degassing (mean: 18 g m-2 day-1). The low degassing rate of the geothermal system is a consequence of the intense hydrothermal alteration observed in the upper 800 m of the system which acts as an impermeable caprock. Highest measured CO2 fluxes (above > 600 g m-2 day-1) have corresponding CH4/CO2 flux ratios similar to mass ratios of sampled gases, which suggest an advective fluid transport. To represent field conditions, a numerical model was also applied to simulate the migration of CO2 towards the surface through a

The high-K calc-alkalic Serra da Lagoinha batholith, States of Ceara and Paraiba (Northeastern region, Brazil): coexistence and mixing of dioritic and quartz monzonitic to granitic magmas

International Nuclear Information System (INIS)

Mariano, Gorki; Sobreira, Mauricio de Nassau de Mattos

1999-01-01

The Serra da Lagoinha batholith (SLB) has an outcrop area of 200 km 2 is located in the Borborema Province, northeastern Brazil, and intrudes schists and phylites at the border of the Cachoeirinha-Salgueiro fold belt. Its southern border is defined by a major curved NE-SW sinistral transcurrent shear zone (Boqueirao dos Cochos) connecting the E-W dextral shear zones of Patos to the north and Pernambuco to the south. The SLB has three lithologic domains: the felsic porphyritic domain composed of K-feldspar megacrystic monzonitic, quartz monzonitic, quartz monzodioritic, granitic to granodioritic rocks; the k-dioritic domain composed of biotite (quartz) dioritic to tonalitic rocks and the hybrid domain composed of monzonitic and biotite (quartz) dioritic rocks. Field evidences show that these lithologic domains were produced by the coexistence and mixing of K-diorites with potassic monzonitic to granodioritic magmas. The mafic rocks are enriched in Nb, ba, and Zr and LREE in relation to the felsic porphyritic rocks. The REE patterns for mafic and felsic rocks are similar and enriched in the LREE in relation to the HREE, with (La/Yb) N varying from 22.43 to 36.10 for the felsic and from 27.21 to 58.87 for the mafic rocks. Al Τ in amphibole geobarometer (Hollister 1987) shows that amphibole crystallization in the SLB occurred at approximately 4.5 kbar. Geothermometry based on the coexistence of amphibole and plagioclase, (Blundy and Holland 1990) gives a temperature of 742 deg C. Whole rock Oxygen isotope data showed average values for mafic of δ 18 O = + 7.9 permil SMOW and for the felsic rocks of δ 18 O + 9.1 permil SMOW , suggesting either isotopic equilibrium of coexistent magmas of distinct sources or crystal fractionation process controlling the evolution from mafic to felsic rocks. Quartz corrected values for the felsic porphyritic rocks averaged δ 18 O = + 9.2 permil, suggesting that the whole rock data represent magmatic values. Sm-Nd systematics show T

Modelling the interplate domain in thermo-mechanical simulations of subduction: Critical effects of resolution and rheology, and consequences on wet mantle melting

Science.gov (United States)

Arcay, Diane

2017-08-01

surface temperature inferred from geothermometry, and 10-40 kJ/mol to reproduce the shallow hot mantle wedge core inferred from conditions of last equilibration of near-primary arc magmas and seismic tomographies. Therefore, an extra process controlling mantle wedge dynamics is needed to satisfy simultaneously the aforementioned observations. A mantle viscosity reduction, by a factor 4-20, caused by metasomatism in the mantle wedge is proposed. From these results, I conclude that the subduction channel down-dip extent, zcoup , should depend on the subduction setting, to be consistent with the observed variability of sub-arc depths of the subducting plate surface.

An evolving magmatic-hydrothermal system in the formation of the Mesozoic Meishan magnetite-apatite deposit in the Ningwu volcanic basin, eastern China

Science.gov (United States)

Liu, Wen-Hao; Jiang, Man-Rong; Zhang, Xiao-Jun; Xia, Yan; Algeo, Thomas J.; Li, Huan

2018-06-01

The Meishan iron deposit contains 338 Mt of iron-ore reserves at 39% Fe and represents the largest magnetite-apatite deposit in the Ningwu Basin of eastern China. Controversy has long existed about whether this deposit had a hydrothermal or iron-oxide melt origin. Iron mineralization is genetically related to plutons that are composed of gabbro-diorite, which were emplaced at 130 ± 1 Ma. These rocks have SiO2 contents of 51.72-54.60 wt%, Na2O contents of 3.47-4.04 wt%, K2O contents of 2.02-2.69 wt%, and K2O/Na2O ratios of 0.51-0.73. These rocks are enriched in LILEs and LREEs and depleted in Nb, Ta, and Ti, which indicates that the magma originated through partial melting of an enriched lithospheric mantle source in a subduction environment. A pattern of decreasing initial Sr isotopic ratios and increasing εNd(t) values with time in Early Cretaceous magmatic rocks of the Ningwu Basin may indicate incorporation of increasing proportions of asthenospheric mantle material into the source magma, which is consistent with the processes of lithospheric thinning and asthenospheric upwelling in eastern China related to Mesozoic subduction of the Paleo-Pacific Plate. Two stages of magnetite are found in the gabbro-diorite: (1) early-crystallized magnetite as euhedral-subhedral crystals in larger clinopyroxene crystals, and (2) later-crystallized magnetite and accompanying ilmenite grains in the voids between plagioclase and clinopyroxene crystals. The formation of magnetite before clinopyroxene, combined with the results of Fe-Ti oxide geothermometry and analysis of magnetite V content, indicates that the oxygen fugacity of the source magma was greater than ΔFMQ +2.2 at an early stage (>640 °C) but decreased to ΔFMQ -2.66 as abundant magnetite crystallized at a later stage (∼489 °C). The early crystallization of magnetite at a high oxygen fugacity does not support a Fenner evolution trend for the primitive magma and diminishes the likelihood of liquid immiscibility

Gas geochemistry of the magmatic-hydrothermal fluid reservoir in the Copahue-Caviahue Volcanic Complex (Argentina)

Science.gov (United States)

Agusto, M.; Tassi, F.; Caselli, A. T.; Vaselli, O.; Rouwet, D.; Capaccioni, B.; Caliro, S.; Chiodini, G.; Darrah, T.

2013-05-01

Copahue volcano is part of the Caviahue-Copahue Volcanic Complex (CCVC), which is located in the southwestern sector of the Caviahue volcano-tectonic depression (Argentina-Chile). This depression is a pull-apart basin accommodating stresses between the southern Liquiñe-Ofqui strike slip and the northern Copahue-Antiñir compressive fault systems, in a back-arc setting with respect to the Southern Andean Volcanic Zone. In this study, we present chemical (inorganic and organic) and isotope compositions (δ13C-CO2, δ15N, 3He/4He, 40Ar/36Ar, δ13C-CH4, δD-CH4, and δD-H2O and δ18O-H2O) of fumaroles and bubbling gases of thermal springs located at the foot of Copahue volcano sampled in 2006, 2007 and 2012. Helium isotope ratios, the highest observed for a Southern American volcano (R/Ra up to 7.94), indicate a non-classic arc-like setting, but rather an extensional regime subdued to asthenospheric thinning. δ13C-CO2 values (from - 8.8‰ to - 6.8‰ vs. V-PDB), δ15N values (+ 5.3‰ to + 5.5‰ vs. Air) and CO2/3He ratios (from 1.4 to 8.8 × 109) suggest that the magmatic source is significantly affected by contamination of subducted sediments. Gases discharged from the northern sector of the CCVC show contribution of 3He-poor fluids likely permeating through local fault systems. Despite the clear mantle isotope signature in the CCVC gases, the acidic gas species have suffered scrubbing processes by a hydrothermal system mainly recharged by meteoric water. Gas geothermometry in the H2O-CO2-CH4-CO-H2 system suggests that CO and H2 re-equilibrate in a separated vapor phase at 200°-220 °C. On the contrary, rock-fluid interactions controlling CO2, CH4 production from Sabatier reaction and C3H8 dehydrogenation seem to occur within the hydrothermal reservoir at temperatures ranging from 250° to 300 °C. Fumarole gases sampled in 2006-2007 show relatively low N2/He and N2/Ar ratios and high R/Ra values with respect to those measured in 2012. Such compositional and

Deposition of talc - kerolite-smectite - smectite at seafloor hydrothermal vent fields: Evidence from mineralogical, geochemical and oxygen isotope studies

Science.gov (United States)

Dekov, V.M.; Cuadros, J.; Shanks, Wayne C.; Koski, R.A.

2008-01-01

Talc, kerolite-smectite, smectite, chlorite-smectite and chlorite samples from sediments, chimneys and massive sulfides from six seafloor hydrothermal areas have been analyzed for mineralogy, chemistry and oxygen isotopes. Samples are from both peridotite- and basalt-hosted hydrothermal systems, and basaltic systems include sediment-free and sediment-covered sites. Mg-phyllosilicates at seafloor hydrothermal sites have previously been described as talc, stevensite or saponite. In contrast, new data show tri-octahedral Mg-phyllosilicates ranging from pure talc and Fe-rich talc, through kerolite-rich kerolite-smectite to smectite-rich kerolite-smectite and tri-octahedral smectite. The most common occurrence is mixed-layer kerolite-smectite, which shows an almost complete interstratification series with 5 to 85% smectitic layers. The smectite interstratified with kerolite is mostly tri-octahedral. The degree of crystal perfection of the clay sequence decreases generally from talc to kerolite-smectite with lower crystalline perfection as the proportion of smectite layers in kerolite-smectite increases. Our studies do not support any dependence of the precipitated minerals on the type/subtype of hydrothermal system. Oxygen isotope geothermometry demonstrates that talc and kerolite-smectite precipitated in chimneys, massive sulfide mounds, at the sediment surface and in open cracks in the sediment near seafloor are high-temperature (> 250????C) phases that are most probably the result of focused fluid discharge. The other end-member of this tri-octahedral Mg-phyllosilicate sequence, smectite, is a moderate-temperature (200-250????C) phase forming deep within the sediment (??? 0.8??m). Chlorite and chlorite-smectite, which constitute the alteration sediment matrix around the hydrothermal mounds, are lower-temperature (150-200????C) phases produced by diffuse fluid discharge through the sediment around the hydrothermal conduits. In addition to temperature, other two

Fluid geochemistry and soil gas fluxes (CO2-CH4-H2S) at a promissory Hot Dry Rock Geothermal System: The Acoculco caldera, Mexico

Science.gov (United States)

Peiffer, L.; Bernard-Romero, R.; Mazot, A.; Taran, Y. A.; Guevara, M.; Santoyo, E.

2014-09-01

The Acoculco caldera has been recognized by the Mexican Federal Electricity Company (CFE) as a Hot Dry Rock Geothermal System (HDR) and could be a potential candidate for developing an Enhanced Geothermal System (EGS). Apart from hydrothermally altered rocks, geothermal manifestations within the Acoculco caldera are scarce. Close to ambient temperature bubbling springs and soil degassing are reported inside the caldera while a few springs discharge warm water on the periphery of the caldera. In this study, we infer the origin of fluids and we characterize for the first time the soil degassing dynamic. Chemical and isotopic (δ18O-δD) analyses of spring waters indicate a meteoric origin and the dissolution of CO2 and H2S gases, while gas chemical and isotopic compositions (N2/He, 3He/4He, 13C, 15N) reveal a magmatic contribution with both MORB- and arc-type signatures which could be explained by an extension regime created by local and regional fault systems. Gas geothermometry results are in agreement with temperature measured during well drilling (260 °C-300 °C). Absence of well-developed water reservoir at depth impedes re-equilibration of gases upon surface. A multi-gas flux survey including CO2, CH4 and H2S measurements was performed within the caldera. Using the graphical statistical analysis (GSA) approach, CO2 flux measurements were classified in two populations. Population A, representing 95% of measured fluxes is characterized by low values (mean: 18 g m- 2 day- 1) while the remaining 5% fluxes belonging to Population B are much higher (mean: 5543 g m- 2 day- 1). This low degassing rate probably reflects the low permeability of the system, a consequence of the intense hydrothermal alteration observed in the upper 800 m of volcanic rocks. An attempt to interpret the origin and transport mechanism of these fluxes is proposed by means of flux ratios as well as by numerical modeling. Measurements with CO2/CH4 and CO2/H2S flux ratios similar to mass ratios

Magmatic-vapor expansion and the formation of high-sulfidation gold deposits: Chemical controls on alteration and mineralization

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Henley, R.W.; Berger, B.R.

2011-01-01

from any external contemporary hydrothermal activity. Subsequent fracturing is localized by the embrittled wallrock to provide high-permeability fracture arrays that constrain vapor expansion with minimization of heat loss. The Sulfide Stage vein sequence is then a consequence of destabilization of metal-vapor species in response to depressurization and decrease in vapor density. The geology, mineralogy, fluid inclusion and stable isotope data and geothermometry for high-sulfidation, bulk-tonnage and lode deposits are quite different from those for epithermal gold-silver deposits such as McLaughlin, California that formed near-surface in groundwater-dominated hydrothermal systems where magmatic fluid has been diluted to less than about 30%. High sulfidation gold deposits are better termed 'Solfataric Gold Deposits' to emphasize this distinction. The magmatic-vapor expansion hypothesis also applies to the phenomenology of acidic geothermal systems in active volcanic systems and equivalent magmatic-vapor discharges on the flanks of submarine volcanoes. ?? 2010.

Estimating the Prospectivity of Geothermal Resources Using the Concept of Hydrogeologic Windows

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Bielicki, Jeffrey; Blackwell, David; Harp, Dylan; Karra, Satish; Kelley, Richard; Kelley, Shari; Middleton, Richard; Person, Mark; Sutula, Glenn; Witcher, James

2016-04-01

In this Geothermal Play Fairways Analysis project we sought to develop new ways to analyze geologic, geochemical, and geophysical data to reduce the risk and increase the prospects of successful geothermal exploration and development. We collected, organized, and analyzed data from southwest New Mexico in the context of an integrated framework that combines the data for various signatures of a geothermal resource into a cohesive analysis of the presence of heat, fluid, and permeability. We incorporated data on structural characteristics (earthquakes, geophysical logs, fault location and age, basement depth), topographic and water table elevations, conservative ion concentrations, and thermal information (heat flow, bottom hole temperature, discharge temperature, and basement heat generation). These data were combined to create maps that indicate structural analysis, slope, geothermometry, and heat. We also mapped discharge areas (to constrain elevations where groundwater may be discharged through modern thermal springs or paleo-thermal springs) and subcrops: possible erosionally- or structurally-controlled breaches in regional-scale aquitards that form the basis of our hydrogeologic windows concept. These two maps were particularly useful in identifying known geothermal systems and narrowing the search for unknown geothermal prospects. We further refined the "prospectivity" of the areas within the subcrops and discharge areas by developing and applying a new method for spatial association analysis to data on known and inferred faults, earthquakes, geochemical thermometers, and heat flow. This new methodology determines the relationships of the location and magnitudes of observations of these data with known geothermal sites. The results of each of the six spatial association analyses were weighted between 0 and 1 and summed to produce a prospectivity score between 0 and 6, with 6 indicating highest geothermal potential. The mean value of prospectivity for all

Geological and hydrogeochemical explorations for geothermal resources in eastern Sabalan, NW Iran.

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Masoumi, Roohangiz

2017-04-01

Geological considerations in the east of Sabalan volcano indicate that the calc-alkaline volcanic-sedimentary units constitute the great volume of the geothermal reservoir in the study district. The rocks suffered argillic alteration acted as cap rocks for this reservoir. In some localities in the study district siliceous (chalcedony and opal) sinters were developed around the orifice of the hot springs. The geothermal fluids in the study district, in terms of physico-chemical parameters, have characteristics which differ from other geothermal fields around the Mount Sabalan particularly in the southern and northwestern districts. These differences are: (a) the measured pH values of the geothermal fluids range from approximately 4.5 to 8.8 signifying a variation from acidity to alkalinity; (b) the measured TDS values of these waters, in comparison with the average TDS values for most types of geothermal systems, are low and the minimum values were recorded in the Viladara area; (c) estimation of concentration values of anions and cations in the selected spring water samples indicate that they have chiefly chloride and bicarbonate anions however, samples from the Sardabeh area contain relatively high sulfate (SO42-) content. The concentration values of rare elements in these waters are noticeable. Selenium has the highest concentration value (170 mg/l) among the rare elements. The maximum concentration values of boron and arsenic were measured to be 7 mg/l and 10 mg/l, respectively. The rest of rare elements have relatively low concentration values in the studied samples. The calculation of solute-based geothermometry was done on the basis of Na-Li, Na-K, Na-K, Ca, and silica for the water samples. The results of all these procedures for estimation of temperature of the geothermal reservoir in the east of Mount Sabalan were relatively very close to one another. Nevertheless, the temperatures determined by the Na-Li and Na-K geothermometric methods are 225°C and 239

Composition and origin of rhyolite melt intersected by drilling in the Krafla geothermal field, Iceland

Science.gov (United States)

Zierenberg, R.A.; Schiffman, P.; Barfod, G.H.; Lesher, C.E.; Marks, N.E.; Lowenstern, Jacob B.; Mortensen, A.K.; Pope, E.C.; Bird, D.K.; Reed, M.H.; Friðleifsson, G.O.; Elders, W.A.

2013-01-01

The Iceland Deep Drilling Project Well 1 was designed as a 4- to 5-km-deep exploration well with the goal of intercepting supercritical hydrothermal fluids in the Krafla geothermal field, Iceland. The well unexpectedly drilled into a high-silica (76.5 % SiO2) rhyolite melt at approximately 2.1 km. Some of the melt vesiculated while extruding into the drill hole, but most of the recovered cuttings are quenched sparsely phyric, vesicle-poor glass. The phenocryst assemblage is comprised of titanomagnetite, plagioclase, augite, and pigeonite. Compositional zoning in plagioclase and exsolution lamellae in augite and pigeonite record changing crystallization conditions as the melt migrated to its present depth of emplacement. The in situ temperature of the melt is estimated to be between 850 and 920 °C based on two-pyroxene geothermometry and modeling of the crystallization sequence. Volatile content of the glass indicated partial degassing at an in situ pressure that is above hydrostatic (~16 MPa) and below lithostatic (~55 MPa). The major element and minor element composition of the melt are consistent with an origin by partial melting of hydrothermally altered basaltic crust at depth, similar to rhyolite erupted within the Krafla Caldera. Chondrite-normalized REE concentrations show strong light REE enrichment and relative flat patterns with negative Eu anomaly. Strontium isotope values (0.70328) are consistent with mantle-derived melt, but oxygen and hydrogen isotope values are depleted (3.1 and −118 ‰, respectively) relative to mantle values. The hydrogen isotope values overlap those of hydrothermal epidote from rocks altered by the meteoric-water-recharged Krafla geothermal system. The rhyolite melt was emplaced into and has reacted with a felsic intrusive suite that has nearly identical composition. The felsite is composed of quartz, alkali feldspar, plagioclase, titanomagnetite, and augite. Emplacement of the rhyolite magma has resulted in partial melting of

Integrated Field Analyses of Thermal Springs

Science.gov (United States)

Shervais, K.; Young, B.; Ponce-Zepeda, M. M.; Rosove, S.

2011-12-01

A group of undergraduate researchers through the SURE internship offered by the Southern California Earthquake Center (SCEC) have examined thermal springs in southern Idaho, northern Utah as well as mud volcanoes in the Salton Sea, California. We used an integrated approach to estimate the setting and maximum temperature, including water chemistry, Ipad-based image and data-base management, microbiology, and gas analyses with a modified Giggenbach sampler.All springs were characterized using GISRoam (tmCogent3D). We are performing geothermometry calculations as well as comparisons with temperature gradient data on the results while also analyzing biological samples. Analyses include water temperature, pH, electrical conductivity, and TDS measured in the field. Each sample is sealed and chilled and delivered to a water lab within 12 hours.Temperatures are continuously monitored with the use of Solinst Levelogger Juniors. Through partnership with a local community college geology club, we receive results on a monthly basis and are able to process initial data earlier in order to evaluate data over a longer time span. The springs and mudpots contained microbial organisms which were analyzed using methods of single colony isolation, polymerase chain reaction, and DNA sequencing showing the impact of the organisms on the springs or vice versa. Soon we we will collect gas samples at sites that show signs of gas. This will be taken using a hybrid of the Giggenbach method and our own methods. Drawing gas samples has proven a challenge, however we devised a method to draw out gas samples utilizing the Giggenbach flask, transferring samples to glass blood sample tubes, replacing NaOH in the Giggenbach flask, and evacuating it in the field for multiple samples using a vacuum pump. We also use a floating platform devised to carry and lower a levelogger, to using an in-line fuel filter from a tractor in order to keep mud from contaminating the equipment.The use of raster

Beyond temperature: Clumped isotope signatures in dissolved inorganic carbon species and the influence of solution chemistry on carbonate mineral composition

Science.gov (United States)

Tripati, Aradhna K.; Hill, Pamela S.; Eagle, Robert A.; Mosenfelder, Jed L.; Tang, Jianwu; Schauble, Edwin A.; Eiler, John M.; Zeebe, Richard E.; Uchikawa, Joji; Coplen, Tyler B.; Ries, Justin B.; Henry, Drew

2015-01-01

“Clumped-isotope” thermometry is an emerging tool to probe the temperature history of surface and subsurface environments based on measurements of the proportion of 13C and 18O isotopes bound to each other within carbonate minerals in 13C18O16O22- groups (heavy isotope “clumps”). Although most clumped isotope geothermometry implicitly presumes carbonate crystals have attained lattice equilibrium (i.e., thermodynamic equilibrium for a mineral, which is independent of solution chemistry), several factors other than temperature, including dissolved inorganic carbon (DIC) speciation may influence mineral isotopic signatures. Therefore we used a combination of approaches to understand the potential influence of different variables on the clumped isotope (and oxygen isotope) composition of minerals.We conducted witherite precipitation experiments at a single temperature and at varied pH to empirically determine 13C-18O bond ordering (Δ47) and δ18O of CO32- and HCO3- molecules at a 25 °C equilibrium. Ab initio cluster models based on density functional theory were used to predict equilibrium 13C-18O bond abundances and δ18O of different DIC species and minerals as a function of temperature. Experiments and theory indicate Δ47 and δ18O compositions of CO32- and HCO3- ions are significantly different from each other. Experiments constrain the Δ47-δ18O slope for a pH effect (0.011 ± 0.001; 12 ⩾ pH ⩾ 7). Rapidly-growing temperate corals exhibit disequilibrium mineral isotopic signatures with a Δ47-δ18O slope of 0.011 ± 0.003, consistent with a pH effect.Our theoretical calculations for carbonate minerals indicate equilibrium lattice calcite values for Δ47 and δ18O are intermediate between HCO3− and CO32−. We analyzed synthetic calcites grown at temperatures ranging from 0.5 to 50 °C with and without the enzyme carbonic anhydrase present. This enzyme catalyzes oxygen isotopic exchange between DIC species and is present in many

Beyond temperature: Clumped isotope signatures in dissolved inorganic carbon species and the influence of solution chemistry on carbonate mineral composition

Science.gov (United States)

Tripati, Aradhna K.; Hill, Pamela S.; Eagle, Robert A.; Mosenfelder, Jed L.; Tang, Jianwu; Schauble, Edwin A.; Eiler, John M.; Zeebe, Richard E.; Uchikawa, Joji; Coplen, Tyler B.; Ries, Justin B.; Henry, Drew

2015-10-01

;Clumped-isotope; thermometry is an emerging tool to probe the temperature history of surface and subsurface environments based on measurements of the proportion of 13C and 18O isotopes bound to each other within carbonate minerals in 13C18O16O22- groups (heavy isotope ;clumps;). Although most clumped isotope geothermometry implicitly presumes carbonate crystals have attained lattice equilibrium (i.e., thermodynamic equilibrium for a mineral, which is independent of solution chemistry), several factors other than temperature, including dissolved inorganic carbon (DIC) speciation may influence mineral isotopic signatures. Therefore we used a combination of approaches to understand the potential influence of different variables on the clumped isotope (and oxygen isotope) composition of minerals. We conducted witherite precipitation experiments at a single temperature and at varied pH to empirically determine 13C-18O bond ordering (Δ47) and δ18O of CO32- and HCO3- molecules at a 25 °C equilibrium. Ab initio cluster models based on density functional theory were used to predict equilibrium 13C-18O bond abundances and δ18O of different DIC species and minerals as a function of temperature. Experiments and theory indicate Δ47 and δ18O compositions of CO32- and HCO3- ions are significantly different from each other. Experiments constrain the Δ47-δ18O slope for a pH effect (0.011 ± 0.001; 12 ⩾ pH ⩾ 7). Rapidly-growing temperate corals exhibit disequilibrium mineral isotopic signatures with a Δ47-δ18O slope of 0.011 ± 0.003, consistent with a pH effect. Our theoretical calculations for carbonate minerals indicate equilibrium lattice calcite values for Δ47 and δ18O are intermediate between HCO3- and CO32-. We analyzed synthetic calcites grown at temperatures ranging from 0.5 to 50 °C with and without the enzyme carbonic anhydrase present. This enzyme catalyzes oxygen isotopic exchange between DIC species and is present in many natural systems. The two

Geochemistry of the thermal springs from Piedras de Lumbre Zone, Chihuahua, Mexico; Geoquimica de los manantiales termales de la zona de Piedras de Lumbre, Chihuahua, Mexico

Energy Technology Data Exchange (ETDEWEB)

Tello Hinojosa, Enrique [Gerencia de Proyectos Geotermoelectricos de la Comision Federal de Electricidad, Morelia (Mexico)

1996-01-01

Chemical analysis of water produced by 12 hot springs in the geothermal areas of Recubichi and Piedras de Lumbre, Chihuahua, Mexico were carried out in order to establish the geochemical characteristic of the groundwater and to know their interaction with deeper geothermal fluids. We made two sampling of water and gases in 1984 and 1995. The chemical composition of waters produced by the springs is of sulfate alkaline type. It was found, according to the Na:K:Mg relative content that most hot springs are located in the partial equilibrium zone, whereas the lowest temperature hot springs shift toward the groundwaters domain. The temperature estimated from gas geothermometry was 187 degrees celsius. It was found that the He has a deep origin, whereas the N{sub 2} is of atmospheric origin. Methane was not detected, suggesting that equilibria between gases and the liquid phase was reached at temperatures over 150 degrees celsius. The chemical compositions for the springs at Recubichi and Piedras de Lumbre zones are similar, so, it suggests that they have the same origin. The water quality of the springs for agricultural use, is classified between C2-S2 and C2-S3 types, that suggest that this water can be used for irrigation. The arsenic element was not detected and the concentration for the boron element is lower that 0.175 ppm. [Espanol] Los analisis quimicos de agua de 12 manantiales y 4 fumarolas de las zonas de Recubichi y Piedras de Lumbre, Chihuahua, Mexico fueron estudiados con el fin de conocer las caracteristicas geoquimicas del acuifero somero y su interaccion con fluidos geotermicos. Se realizaron 2 muestreos tanto de agua como de gases en 1984 y 1995. En ambos muestreos se encontro que la composicioon quimica del agua de todos los manantiales es del tipo sulfatado-sodico. De acuerdo con el contenido relativo de Na:K:Mg el agua de los manantiales mas calientes (93 grados celsius), se ubica en la zona de equilibrio parcial, mientras que en los de menor

Geochemistry of the thermal springs from San Antonio El Bravo zone, Chihuahua, Mexico; Geoquimica de manantiales termales de la zona de San Antonio El Bravo, Chihuahua, Mexico

Energy Technology Data Exchange (ETDEWEB)

Tello Hinojosa, Enrique [Gerencia de Proyectos Geotermoelectricos de la Comision Federal de Electricidad, Morelia (Mexico)

1996-05-01

Isotopic and chemical analysis o water produced by 14 springs in the San Antonio El Bravo, Chihuahua, Mexico geothermal area, were carried out in order to establish the geochemical characteristics of the groundwater and to know their interaction with deeper geothermal fluids. We made two samplings of water and gases in 1984 and 1995. The chemical composition of waters produced by the springs in of sodium-bicarbonate-chloride type. It was found, according to the Na:K:Mg relative content, that most hot springs are located in the partial equilibrium zone, whereas the lowest temperature hot springs shift toward the groundwaters domain. The temperature estimated from gas geothermometry was 129 degrees celsius. The isotopic composition at Ojo Caliente and Infiernito springs presents enrichment in {delta}{sup 18}O, product rock-water interaction at high temperature. The Agua Roque spring is located in the line of meteoric waters. Analysis of metals was carried out too, the concentration of gold element is 0.09 mg/l in Ojo Caliente and Infiernito springs, whereas silver, aluminum and iron elements were not detected. The water quality of the springs for agricultural use, is classified between C2-S1, C3-S1, C3- S2, C4-S3 and C4-S4 types, that suggests that only the water from Agua Roque can be used for irrigation. The arsenic element was not detected but the concentration of the boron element is high for irrigation use (2.39 ppm). [Espanol] Los analisis quimicos e isotopicos de agua de 14 manantiales de la zona de San Antonio El Bravo. Chihuahua, Mexico, fueron realizados con el fin de conocer las caracteristicas geoquimicas del acuifero somero y su interaccion con fluidos geotermicos. Se realizaron 2 muestreos tanto de agua como de gases en 1984 y 1995. En ambos muestreos se encontro que la composicion quimica del agua de todos los manantiales es del tipo bicarbonatado-clorurado-sodico. De acuerdo con el contenido relativo de Na:K:Mg el agua de los manantiales mas calientes

Study of REE behaviors, fluid inclusions, and O, S stable Isotopes in Zafar-abad iron skarn deposit, NW Divandarreh, Kordestan province

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Mehrdad Barati

2014-10-01

Full Text Available Introduction The Zafar-abad iron ore deposit, situated in the NW part of Divandarreh (lat. 36°01'14" and long. 46°58'22". The ore body is located on the northern margin of the Sanandaj-Sirjan igneous metamorphic zone. The Zafar-abad Fe-skarn deposit is one of the important, medium- size mineral deposits in western Iran. REE patterns of skarn magnetite were among others studied in Skarn deposit by (Taylor, 1979 Hydrothermal alteration and fluid-rock interaction significantly affect total contents of REE and their patterns in fluids. Moreover, fractionation of REE by chemical complication, adsorption effects and redox reactions are characteristic processes determining REE behavior during crystallization. Stable isotope data for oxygen and sulfur have been widely used with great success to trace the origin and evolution history of paleo-hydrothermal fluids of meteoric, magmatic, and metamorphic. Materials and methods The present study investigates REE and stable Isotope geochemistry of magnetite and pyrite in Zafar-abad deposit and temperature of trapped fluid inclusions based on geothermometry analysis. In order to study the major, trace and REE compositions of Zafar-abad magnetite, twelve samples were collected from surface of ore exposures. The emphasis during sampling was on ores with primary textures. Discussion The Zafar-abad district is situated in Mesozoic and Cenozoic sedimentary, meta-sedimentary and meta-igneous rocks in Sanandaj-Sirjan igneous metamorphic zone. Sedimentary sequences dominantly composed of calcareous and conglomerate rocks. Various meta-sedimentary rocks are intercalated with the sedimentary rocks, and comprise biotite and muscovite-rich schist, calc-schist, calc-silicate rock. Several distinct ductile tectonic fabrics have been identified around the Zafar-abad deposit. The main ore body at Zafar-abad is in the form of a roughly horizontal, discordant, lens to tabular-shaped body plunging 10° NW, where it appears to