Raster Files for Utah Play Fairway Analysis

DOE Data Explorer

Wannamaker, Phil

2017-06-16

This submission contains raster files associated with several datasets that include earthquake density, Na/K geothermometers, fault density, heat flow, and gravity. Integrated together using spatial modeler tools in ArcGIS, these files can be used for play fairway analysis in regard to geothermal exploration.

Gas chemistry and thermometry of the Cerro Prieto, Mexico, geothermal field

USGS Publications Warehouse

Nehring, N.L.; D'Amore, F.

1984-01-01

Gas compositions of Cerro Prieto wells in 1977 reflected strong boiling in the reservoir around wells M-20 and M-25. This boiling zone appeared to be collapsing in 1982 when a number of wells in this area of the field were shut-in. In 1977 and 1982, gas compositions also showed boiling zones corresponding to faults H and L postulated by Halfman et al. (1982). Four gas geothermometers were applied, based on reservoir equilibria and calculated fugacities. The Fisher - Tropsch reaction predicted high temperatures and appeared to re-equilibrate slowly, whereas the H2S reaction predicted low temperatures and appeared to re-equilibrate rapidly. Hydrogen and NH3 reactions were intermediate. Like gas compositions, the geothermometers reflected reservoir processes, such as boiling. Surface gas compositions are related to well compositions, but contain large concentrations of N2 originating from air dissolved in groundwater. The groundwater appears to originate in the east and flow over the production field before mixing with reservoir gases near the surface. ?? 1984.

DOE Office of Scientific and Technical Information (OSTI.GOV)

Simmons, Stuart F.; Spycher, Nicolas; Sonnenthal, Eric

This report summarizes the results of Phase I work for a go/no go decision on Phase II funding. In the first objective, we assessed the extent to which fluid-mineral equilibria controlled deep water compositions in geothermal systems across the Great Basin. Six systems were evaluated: Beowawe; Desert Peak; Dixie Valley; Mammoth; Raft River; Roosevelt. These represent a geographic spread of geothermal resources, in different geological settings and with a wide range of fluid compositions. The results were used for calibration/reformulation of chemical geothermometers that reflect the reservoir temperatures in producing reservoirs. In the second objective, we developed a reactive -transportmore » model of the Desert Peak hydrothermal system to evaluate the processes that affect reservoir fluid geochemistry and its effect on solute geothermometry. This included testing geothermometry on “reacted” thermal water originating from different lithologies and from near-surface locations where the temperature is known from the simulation. The integrated multi-component geothermometer (GeoT, relying on computed mineral saturation indices) was tested against the model results and also on the systems studied in the first objective.« less

Constructing the deep temperature section of the Travale geothermal area in Italy, with the use of an electromagnetic geothermometer

NASA Astrophysics Data System (ADS)

Spichak, V. V.; Zakharova, O. K.

2015-01-01

The technology of electromagnetic geothermometer is applied for constructing the two-dimensional (2D) section of temperature in the Travale geothermal region in Italy up to a depth of 10 km. The joint analysis of this section, together with the previously constructed model of electric resistivity suggests that the heat transfer in the Travale region is rendered by the overheated vapor-gas fluids instead of liquid fluids as it was previously believed based on the interpretation of the resistivity model. Another important conclusion consists in the fact that, instead of two geothermal reservoirs, whose existence was previously tentatively inferred from the interpretation of the electromagnetic and seismic data, it is likely that there is a single deep reservoir with a shallow (near-surface) offshoot. From the constructed temperature distribution it can be seen that the temperature below a depth of 4 km exceeds 500°C, which indicates that drilling down to these depths could be useful for the subsequent exploitation of this geothermal reservoir.

Tularosa Basin Play Fairway Analysis: Water Chemistry

DOE Data Explorer

Adam Brandt

2015-12-15

This shapefile contains 409 well data points on Tularosa Basin Water Chemistry, each of which have a location (UTM), temperature, quartz and Potassium/Magnesium geothermometer; as well as concentrations of chemicals like Mn, Fe, Ba, Sr, Cs, Rb, As, NH4, HCO3, SO4, F, Cl, B, SiO2, Mg, Ca, K, Na, and Li.

Tularosa Basin Play Fairway Analysis: Partial Basin and Range Heat and Zones of Critical Stress Maps

DOE Office of Scientific and Technical Information (OSTI.GOV)

Adam Brandt

Interpolated maps of heat flow, temperature gradient, and quartz geothermometers are included as TIF files. Zones of critical stress map is also included as a TIF file. The zones are given a 5km diameter buffer. The study area is only a part of the Basin and Range, but it does includes the Tularosa Basin.

A new illite geothermometer

DOE Office of Scientific and Technical Information (OSTI.GOV)

Ballantyne, Judith M.; Moore, Joseph N.

1988-01-01

Sericite, either as illite or illite/smectite, is ubiquitous in geothermal systems. Theoretical Ca- and Na-smectite contents of non-expanding geothermal sericites have been calculated from published electron microprobe analyses. Geothermal sericites can be modeled as solid solutions of muscovite and smectite. For those sericites that fit the model, the amount of smectite in solid solution is related to temperature by the expression TºC = 1000/(0.45LogX{sub smectite} + 2.38) – 273. The temperature dependence of illite interlayer chemistry suggests a related temperature dependence of the K, Na and Ca content of geothermal fluids. The original data used by Fournier and Truesdell (1973)more » to derive the empirical Na-K-Ca geothermometer for geothermal fluids can be modeled equally well by an equation incorporating the equilibrium constant for the reaction of smectite to illite: T ºC = 1.145*10{sup 3}/([0.35LogNa + 0.175LogCa – 0.75LogK] + 1.51) – 273, where the concentration units are molalities. This supports the hypothesis that illite and illite/smectite are important controls on the concentrations of Na, K and Ca in geothermal fluids.« less

SE Great Basin Play Fairway Analysis

DOE Data Explorer

Adam Brandt

2015-11-15

This submission includes a Na/K geothermometer probability greater than 200 deg C map, as well as two play fairway analysis (PFA) models. The probability map acts as a composite risk segment for the PFA models. The PFA models differ in their application of magnetotelluric conductors as composite risk segments. These PFA models map out the geothermal potential in the region of SE Great Basin, Utah.

Oxygen and hydrogen isotope geochemistry of zeolites

NASA Technical Reports Server (NTRS)

Karlsson, Haraldur R.; Clayton, Robert N.

1990-01-01

Oxygen and hydrogen isotope ratios for natural samples of the zeolites analcime, chabazite, clinoptilolite, laumontite, mordenite, and natrolite have been obtained. The zeolite samples were classified into sedimentary, hydrothermal, and igneous groups. The ratios for each species of zeolite are reported. The results are used to discuss the origin of channel water, the role of zeolites in water-rock interaction, and the possibility that a calibrated zeolite could be used as a low-temperature geothermometer.

Program and Abstracts for Clay Minerals Society 28th Annual Meeting

NASA Technical Reports Server (NTRS)

1991-01-01

This volume contains abstracts that were accepted for presentation at the annual meeting. Some of the main topics covered include: (1) fundamental properties of minerals and methods of mineral analysis; (2) surface chemistry; (3) extraterrestrial clay minerals; (4) geothermometers and geochronometers; (5) smectite, vermiculite, illite, and related reactions; (6) soils and clays in environmental research; (7) kaolinite, halloysite, iron oxides, and mineral transformations; and (8) clays in lakes, basins, and reservoirs.

Estimation of deepwater temperature and hydrogeochemistry of springs in the Takab geothermal field, West Azerbaijan, Iran.

PubMed

Sharifi, Reza; Moore, Farid; Mohammadi, Zargham; Keshavarzi, Behnam

2016-01-01

Chemical analyses of water samples from 19 hot and cold springs are used to characterize Takab geothermal field, west of Iran. The springs are divided into two main groups based on temperature, host rock, total dissolved solids (TDS), and major and minor elements. TDS, electrical conductivity (EC), Cl(-), and SO4 (2-) concentrations of hot springs are all higher than in cold springs. Higher TDS in hot springs probably reflect longer circulation and residence time. The high Si, B, and Sr contents in thermal waters are probably the result of extended water-rock interaction and reflect flow paths and residence time. Binary, ternary, and Giggenbach diagrams were used to understand the deeper mixing conditions and locations of springs in the model system. It is believed that the springs are heated either by mixing of deep geothermal fluid with cold groundwater or low conductive heat flow. Mixing ratios are evaluated using Cl, Na, and B concentrations and a mass balance approach. Calculated quartz and chalcedony geothermometer give lower reservoir temperatures than cation geothermometers. The silica-enthalpy mixing model predicts a subsurface reservoir temperature between 62 and 90 °C. The δ(18)O and δD (δ(2)H) are used to trace and determine the origin and movement of water. Both hot and cold waters plot close to the local meteoric line, indicating local meteoric origin.

Characterization of Organic Materials in the Xenolithic Clasts in Sharps (H3.4) Meteorite Using Micro-Raman Spectroscopy

NASA Technical Reports Server (NTRS)

Chan, Q. H. S.; Zolensky, M. E.; Bodnar, R. J.; Kebukawa, Y.

2015-01-01

Graphitization of carbon is an irreversible process which alters the structure of graphitic materials in response to the increase in metamorphic grade (temperature and/or pressure). Carbonaceous materials offer a reliable geothermometer as their Raman spectra change systematically with increasing metamorphic grade. In this study, we identified carbonaceous materials in the xenolithic clasts in Sharps and interpreted their metamorphic history by revealing the structural organization (order) of the polyaromatic organic phases using micro-Raman spectroscopy.

Characterization of Organic Materials in the Xenolithic Clasts in Sharps (H3.4) Meteorite Using Microraman Spectroscopy

NASA Technical Reports Server (NTRS)

Chan, Q. H. S.; Zolensky, M. E.; Bodnar, R. J.; Kebukawa, Y.

2015-01-01

Graphitization of carbon is an irreversible process which alters the structure of graphitic materials in response to the increase in metamorphic grade (temperature and/or pressure). Carbonaceous materials offer a reliable geothermometer as their Raman spectra change systematically with increasing metamorphic grade [1-3]. In this study, we identified carbonaceous materials in the xenolithic clasts in Sharps and interpreted their metamorphic history by revealing the structural organization (order) of the polyaromatic organic phases using µ-Raman spectroscopy.

Techniques for the conversion to carbon dioxide of oxygen from dissolved sulfate in thermal waters

USGS Publications Warehouse

Nehring, N.L.; Bowen, P.A.; Truesdell, A.H.

1977-01-01

The fractionation of oxygen isotopes between dissolved sulfate ions and water provides a useful geothermometer for geothermal waters. The oxygen isotope composition of dissolved sulfate may also be used to indicate the source of the sulfate and processes of formation. The methods described here for separation, purification and reduction of sulfate to prepare carbon dioxide for mass spectrometric analysis are modifications of methods by Rafter (1967), Mizutani (1971), Sakai and Krouse (1971), and Mizutani and Rafter (1969). ?? 1976.

Delineating Spatial Patterns in the Yellowstone Hydrothermal System using Geothermometry

NASA Astrophysics Data System (ADS)

King, J.; Hurwitz, S.; Lowenstern, J. B.

2015-12-01

Yellowstone National Park is unmatched with regard to its quantity of active hydrothermal features. Origins of thermal waters in its geyser basins have been traced to mixing of a deep parent water with meteoric waters in shallow local reservoirs (Fournier, 1989). A mineral-solution equilibrium model was developed to calculate water-rock chemical re-equilibration temperatures in these shallow reservoirs. We use the GeoT program, which uses water composition data as input to calculate saturation indices of selected minerals; the "best-clustering" minerals are then statistically determined to infer reservoir temperatures (Spycher et al., 2013). We develop the method using water composition data from Heart Lake Geyser Basin (HLGB), for which both chemical and isotopic geothermometers predict a reservoir water temperature of 205°C ± 10°C (Lowenstern et al., 2012), and minerals found in drill cores in Yellowstone's geyser basins. We test the model for sensitivity to major element composition, pH, Total Inorganic Carbon (TIC) and selected minerals to optimize model parameters. Calculated temperatures are most accurate at pH values below 9.0, and closely match the equilibrium saturation indices of quartz, stilbite, microcline, and albite. The model is optimized with a TIC concentration that is consistent with the mass of diffuse CO2 flux in HLGB (Lowenstern et al., 2012). We then use water compositions from other thermal basins in Yellowstone in search of spatial variations in reservoir temperatures. We then compare the calculated temperatures with various SiO2 and cation geothermometers.

Zr and Hf diffusion in rutile

NASA Astrophysics Data System (ADS)

Cherniak, D. J.; Manchester, J.; Watson, E. B.

2007-09-01

Chemical diffusion of Zr and Hf under anhydrous conditions has been measured in synthetic and natural rutile. The sources of diffusant used were hafnon or zircon powders or a hafnon-rutile mixture. Experiments were run in crimped Pt capsules in air, or in sealed silica glass capsules with solid buffers (to buffer at NNO or QFM). Rutherford Backscattering Spectrometry (RBS) was used to measure Zr and Hf diffusion profiles. From these measurements, the following Arrhenius relations were obtained: For Zr diffusion parallel to c, over the temperature range 750-1100 °C DZr¦c = 9.8 × 10 - 15 exp(- 170 ± 30 kJ mol - 1 /RT) m 2 s - 1 For Hf diffusion parallel to c, over the temperature range 800-1000 °C DHf¦c = 9.1 × 10 - 15 exp(- 169 ± 36 kJ mol - 1 /RT) m 2 s - 1 For Hf diffusion normal to c, over the temperature range 750-1050 °C DHf⊥c = 2.5 × 10 - 12 exp(- 227 ± 62 kJ mol - 1 /RT) m 2 s - 1 . Diffusivities for experiments buffered at QFM and NNO are similar to those run in air. Diffusivities in synthetic and natural rutile are likewise similar, indicating that these findings can be applied directly in determining Zr diffusivities in rutile in natural systems. These data indicate that rutile should be moderately retentive of Zr chemical signatures, with Zr diffusivities within an order of magnitude of those for Pb in rutile over most geologic conditions. When applied in evaluation of the relative robustness of the recently developed Zr-in-rutile geothermometer [T. Zack, R. Moraes, A. Kronz, Temperature dependence of Zr in rutile: empirical calibration of a rutile thermometer, Contributions to Mineralogy and Petrology 148 (2004) 471-488., E.B. Watson, D.A. Wark, J.B. Thomas, Crystallization thermometers for zircon and rutile, Contributions to Mineralogy and Petrology 151 (2006) 413-433.], these findings suggest that Zr concentrations in rutile will be somewhat more likely to be affected by later thermal disturbance than the geothermometer based on Zr concentrations in titanite [L. Hayden, E.B.Watson, D.A. Wark, A thermobarometer for sphene, Abstract, 16th V.M. Goldschmidt Conference (2006).], and much less resistant to diffusional alteration subsequent to crystallization than the Ti-in-zircon geothermometer [E.B. Watson, D.A. Wark, J.B. Thomas, Crystallization thermometers for zircon and rutile, Contributions to Mineralogy and Petrology 151 (2006) 413-433., E.B.Watson, T.M.Harrison, Zircon thermometer reveals minimum melting conditions on earliest Earth, Science 308 (2005) 841-844.].

Comparison of early exploration at Platanares (Honduras) and Wairakei (New Zealand)

USGS Publications Warehouse

Truesdell, A.H.; Glover, R.B.; Janik, C.J.; Brown, K.L.; Goff, F.

1989-01-01

Early exploration at Wairakei, New Zealand, is compared with the present state of exploration of Platanares, Honduras. In retrospect, geothermometer temperatures favor Platanares (e.g., 220 vs. 190??C for Na-K-Ca), but two 600-m drill holes encountered lower temperatures (160??C). Wairakei, explored before the advent of chemical geothermometry, also had disappointing early drilling results (but better than Platanares; one of the first six holes hit T > 180??C). The Wairakei drilling program was nevertheless continued at full speed and by well 20 a successful drilling strategy was discovered.

Some petrological aspects of Imbrium stratigraphy

NASA Technical Reports Server (NTRS)

Ridley, W. I.

1977-01-01

Descriptions are given of the petrochemistry of two Apennine Front breccias, both ejected to the surface during excavation of Spur Crater. The first clast type is breccia number 15445, a spinel pyroxenite whose mineralogy and petrochemistry are consistent with the original rock type being a garnet pyroxenite. The second rock, breccia 15459, is plutonic norite, in which coarsely exsolved inverted pigeonite is associated with anorthitic plagioclase. Application of mineral geothermometers indicates crystallization of these rocks below 1100 C; hence their textures probably developed largely by solid state recrystallization during impact-metamorphism.

Exsolved silicate and oxide phases from clinopyroxenes in a single Hawaiian xenolith: Implications for oxidation state of the Hawaiian upper mantle

NASA Astrophysics Data System (ADS)

Sen, Gautam; Jones, Robert E.

1988-01-01

A single garnet-bearing clinopyroxenite xenolith from the Salt Lake crater on Oahu, Hawaii, contains two distinct types of clinopyroxene; one contains exsolved garnet, ilmenite, and magnetite, and the other contains exsolved hercynite-pleonaste spinel, orthopyroxene, and ilmenite. Application of mineral geothermometers, barometers, and oxygen barometers to this unusual combination of exsolved phases defines the following conditions of last mantle equilibration of this xenolith: P = 19 kbar, T =1153 °C, and log10fO2 = -9.7.

Mixing models and ionic geothermometers applied to warm (up to 60°C) springs: Jordan Rift Valley, Israel

USGS Publications Warehouse

Mazor, E.; Levitte, D.; Truesdell, A.H.; Healy, J.; Nissenbaum, A.

1980-01-01

No indications are available for the existence of above-boiling geothermal systems in the Jordan Rift Valley. Slightly higher than observed temperatures are concluded for a deep component at the springs of Hammat Gader (67°C), Gofra (68°C), the Russian Garden (40°C), and the Yesha well (53–65°C). These temperatures may encourage further developments for spas and bathing installations and, to a limited extent, for space heating, but are not favorable for geothermal power generation.

Geothermometry of Kilauea Iki lava lake, Hawaii

USGS Publications Warehouse

Helz, R.T.; Thornber, C.R.

1987-01-01

Data on the variation of temperature with time and in space are essential to a complete understanding of the crystallization history of basaltic magma in Kilauea Iki lava lake. Methods used to determine temperatures in the lake have included direct, downhole thermocouple measurements and Fe-Ti oxide geothermometry. In addition, the temperature variations of MgO and CaO contents of glasses, as determined in melting experiments on appropriate Kilauean samples, have been calibrated for use as purely empirical geothermometers and are directly applicable to interstitial glasses in olivine-bearing core from Kilauea Iki. The uncertainty in inferred quenching temperatures is ??8-10?? C. Comparison of the three methods shows that (1) oxide and glass geothermometry give results that are consistent with each other and consistent with the petrography and relative position of samples, (2) downhole thermo-couple measurements are low in all but the earliest, shallowest holes because the deeper holes never completely recover to predrilling temperatures, (3) glass geothermometry provides the greatest detail on temperature profiles in the partially molten zone, much of which is otherwise inaccessible, and (4) all three methods are necessary to construct a complete temperature profile for any given drill hole. Application of glass-based geothermometry to partially molten drill core recovered in 1975-1981 reveals in great detail the variation of temperature, in both time and space, within the partially molten zone of Kilauea Iki lava lake. The geothermometers developed here are also potentially applicable to glassy samples from other Kilauea lava lakes and to rapidly quenched lava samples from eruptions of Kilauea and Mauna Loa. ?? 1987 Springer-Verlag.

Geothermometry of Kilauea Iki lava lake, Hawaii

NASA Astrophysics Data System (ADS)

Helz, Rosalind Tuthill; Thornber, Carl R.

1987-10-01

Data on the variation of temperature with time and in space are essential to a complete understanding of the crystallization history of basaltic magma in Kilauea Iki lava lake. Methods used to determine temperatures in the lake have included direct, downhole thermocouple measurements and Fe-Ti oxide geothermometry. In addition, the temperature variations of MgO and CaO contents of glasses, as determined in melting experiments on appropriate Kilauean samples, have been calibrated for use as purely empirical geothermometers and are directly applicable to interstitial glasses in olivine-bearing core from Kilauea Iki. The uncertainty in inferred quenching temperatures is ±8-10° C. Comparison of the three methods shows that (1) oxide and glass geothermometry give results that are consistent with each other and consistent with the petrography and relative position of samples, (2) downhole thermo-couple measurements are low in all but the earliest, shallowest holes because the deeper holes never completely recover to predrilling temperatures, (3) glass geothermometry provides the greatest detail on temperature profiles in the partially molten zone, much of which is otherwise inaccessible, and (4) all three methods are necessary to construct a complete temperature profile for any given drill hole. Application of glass-based geothermometry to partially molten drill core recovered in 1975 1981 reveals in great detail the variation of temperature, in both time and space, within the partially molten zone of Kilauea Iki lava lake. The geothermometers developed here are also potentially applicable to glassy samples from other Kilauea lava lakes and to rapidly quenched lava samples from eruptions of Kilauea and Mauna Loa.

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

NASA Astrophysics Data System (ADS)

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.

Assessment of the geothermal resources of the Socialist Republic of Vietnam

DOE Office of Scientific and Technical Information (OSTI.GOV)

Flynn, T.; Tien, Phan Cu; Schochert, D.

1997-12-31

More than 125 thermal springs, with temperatures greater than 30{degrees}C have been identified and catalogued by the General Department of Geology of Vietnam. Subsurface data are limited and fewer than 10 areas have been identified, on the basis of chemical geothermometers, as capable of supporting electric power production. Six sites in south-central Vietnam have recently been selected for exploration to determine their development potential for electrical power generation. Selected criteria included surface features, chemical geothermometers, proximity to regional faults trends, and regional requirements for electric power. Site visits were conducted to a total of eight areas in south central Vietnammore » where collateral economic developments suggest the need for a local, reliable source of electricity. Physical and visual information on geothermal springs and wells in Vietnam was compared to Nevada`s geothermal resources. Surface geothermal manifestations in Vietnam appear remarkably similar to those in Nevada. Outcrops adjacent to the geothermal areas indicate that Mesozoic-age granites are the most likely basement rocks. Quaternary basalts mapped throughout the study area may be responsible for the thermal anomaly. Initial exploration efforts will focus on three of the six sites, which together may be able to produce 40 to 60 MWe. A cooperative research program with selected Vietnamese governmental agencies includes geologic mapping, surface geophysical and geochemical surveys, and a graduated schedule of drilling programs, ranging in depth from 100 to 1,000 m. Results will be used to define a detailed, deep drilling and testing program at the three prime sites. Development of geothermal power in this region will boost local economic recovery and add stability to the national electric grid.« less

Generation of Primary Kilauea Magmas: Constraints on Pressure, Temperature and Composition of Melts

NASA Astrophysics Data System (ADS)

Gudfinnsson, G. H.; Presnall, D. C.

2004-12-01

Picrite glasses from the submarine extension of Kilauea, Puna Ridge, which contain up to 15.0 wt% MgO, are the most magnesian glass samples reported from Hawaii. Their compositions form a distinct olivine fractionation trend. A comparison of this trend with phase relations of garnet lherzolite in the CaO-MgO-Al2O3-SiO2 (CMAS) and CaO-MgO-Al2O3-SiO2-Na2O-FeO (CMASNF) system indicates that melts parental to the Hawaiian picrites are produced by melting of a garnet lherzolite source at a pressure of 5 ± 1 GPa. The primary melt composition for Kilauea proposed by Clague et al. (1995), which has 18.4 wt% MgO, is close to the expected 5 GPa melt composition. By using the pressure-independent CMASNF geothermometer (Gudfinnsson and Presnall, 2001), we obtain a temperature of formation of 1450° C for the most magnesian Puna Ridge glass after correction for the presence of 0.4 wt% H2O and 0.7 wt% CO2. This assumes that the glass is not much modified after separation from the lherzolite source. However, comparison with phase relations in the CMAS system strongly suggests that the most magnesian Puna Ridge glasses are the product of some olivine fractionation, and therefore give temperature considerably lower than that of the source. When applied to the proposed Kilauea primary melt composition of Clague et al. (1995), the CMASNF geothermometer gives a melting temperature of 1596° C or about 1565° C after correction for the presence of volatiles. This compares well with the anhydrous solidus temperature of 1600 ± 15° C at 5 GPa for the fertile KR4003 lherzolite (Lesher et al., 2003), which has the complete garnet lherzolite phase assemblage present at the solidus at this pressure. This consistency supports use of phase relations from the CMAS system and the CMASNF geothermometer to the Puna Ridge picrite compositions. With the pressure and temperature of melting known, one can calculate the potential temperature of the Hawaiian mantle, provided certain conditions are met. The calculation assumes that the temperature at the point of melt segregation is close to the temperature of the solid adiabat. If extensive melting has occurred prior to the segregation, this will be incorrect. Secondly, it is assumed that the melting is occurring at the non-conducting part of the geotherm. Provided this is the case and the Kilauea primary melt composition truly represents a near-primary melt composition, we derive a potential temperature for the mantle beneath Kilauea of about 1500° C. The very high temperature and pressure conditions for magma generation at Hawaii appear to be unmatched by any other currently active volcanism on the Earth. Thus, of all the candidates for plume status, Hawaii appears to be the most robust.

Assessment of geothermal resources at Newcastle, Utah

USGS Publications Warehouse

Blackett, Robert E.; Shubat, Michael A.; Chapman, David S.; Forster, Craig B.; Schlinger, Charles M.

1989-01-01

Integrated geology, geophysics, and geochemistry studies in the Newcastle area of southwest Utah are used to develop a conceptual geologic model of a blind, moderate-temperature hydrothermal system. Studies using 12 existing and 12 new, thermal gradient test holes, in addition to geologic mapping, gravity surveys, and other investigations have helped define the thermal regime. Preliminary results indicate that the up-flow region is located near the west-facing escarpment of an adjacent mountain range, probably related to the bounding range-front fault. Chemical geothermometers suggest equilibration temperatures ranging from 140??C to 170??C. The highest temperature recorded in the system is 130??C from an exploration well drilled by the Unocal Corporation.

The First Finding of Sapphirine in Granulites of the Angara-Kan Block: Evidence of Ultra-High-Temperature Metamorphism in the SW Siberian Craton

NASA Astrophysics Data System (ADS)

Sukhorukov, V. P.; Gladkochub, D. P.; Turkina, O. M.

2018-04-01

This work reports the first discovery of sapphirine-bearing mineral parageneses in granulites of the Angara-Kan block, information on the mineral assemblage of rocks, and the mineral composition. Based on mineral geothermometers utilizing alumina content in orthopyroxene, reconstruction of the composition of ternary feldspar, and the titanium content in zircon, it was revealed that the peak temperatures of metamorphism reached 1100°C, after which the rocks underwent cooling under sub-isobaric conditions. It is assumed that the pulse of ultra-high-temperature metamorphism correlates with processes of extension and intraplate magmatism during the age interval of 1.78-1.75 Ga.

Kerogen maturation and incipient graphitization of hydrocarbon source rocks in the Arkoma Basin, Oklahoma and Arkansas: A combined petrographic and Raman spectrometric study

USGS Publications Warehouse

Spotl, C.; Houseknecht, D.W.; Jaques, R.C.

1998-01-01

Dispersed kerogen of the Woodford-Chattanooga and Atoka Formations from the subsurface of the Arkoma Basin show a wide range of thermal maturities (0.38 to 6.1% R(o)) indicating thermal conditions ranging from diagenesis to incipient rock metamorphism. Raman spectral analysis reveals systematic changes of both the first- and second-order spectrum with increasing thermal maturity. These changes include a pronounced increase in the D/O peak height ratio accompanied by a narrowing of the D peak, a gradual decrease in the D/O peak width ratio, and a shift of both peaks toward higher wave numbers. Second-order Raman peaks, though less intensive, also show systematic peak shifting as a function of R(o). These empirical results underscore the high potential of Raman spectrometry as a fast and reliable geothermometer of mature to supermature hydrocarbon source rocks, and as an indicator of thermal maturity levels within the anchizone.Dispersed kerogen of the Woodford-Chattanooga and Atoka Formations from the subsurface of the Arkoma Basin show a wide range of thermal maturities (0.38 to 6.1% Ro) indicating thermal conditions ranging from diagenesis to incipient rock metamorphism. Raman spectral analysis reveals systematic changes of both the first- and second-order spectrum with increasing thermal maturity. These changes include a pronounced increase in the D/O peak height ratio accompanied by a narrowing of the D peak, a gradual decrease in the D/O peak width ratio, and a shift of both peaks toward higher wave numbers. Second-order Raman peaks, though less intensive, also show systematic peak shifting as a function of Ro. These empirical results underscore the high potential of Raman spectrometry as a fast and reliable geothermometer of mature to supermature hydrocarbon source rocks, and as an indicator of thermal maturity levels within the anchizone.

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

USGS Publications Warehouse

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.

Empirical calibration of the clinopyroxene-garnet magnesium isotope geothermometer and implications

NASA Astrophysics Data System (ADS)

Li, Wang-Ye; Teng, Fang-Zhen; Xiao, Yilin; Gu, Hai-Ou; Zha, Xiang-Ping; Huang, Jian

2016-07-01

The large equilibrium Mg isotope fractionation between clinopyroxene and garnet observed in eclogites makes it a potential high-precision geothermometer, but calibration of this thermometer by natural samples is still limited. Here, we report Mg isotopic compositions of eclogite whole rocks as well as Mg and O isotopic compositions of clinopyroxene and garnet separates from 16 eclogites that formed at different temperatures from the Dabie orogen, China. The whole-rock δ26Mg values vary from -1.20 to +0.10 ‰. Among them, 11 samples display limited δ26Mg variations from -0.36 to -0.17 ‰, similar to those of their protoliths. The mineral separates exhibit very different δ26Mg values, from -0.39 to +0.39 ‰ for clinopyroxenes and from -1.94 to -0.81 ‰ for garnets. The clinopyroxene-garnet Mg isotope fractionation (Δ26Mgclinopyroxene-garnet = δ26Mgclinopyroxene-δ26Mggarnet) varies from 1.05 to 2.15 ‰. The clinopyroxene-garnet O isotope fractionation (Δ18Oclinopyroxene-garnet = δ18Oclinopyroxene-δ18Ogarnet) varies from -1.01 to +0.98 ‰. Equilibrium Mg isotope fractionation between clinopyroxene and garnet in the investigated samples is selected based on both the δ26Mgclinopyroxene versus δ26Mggarnet plot and the state of O isotope equilibrium between clinopyroxene and garnet. The equilibrium Δ26Mgclinopyroxene-garnet and corresponding temperature data obtained in this study, together with those available so far in literatures for natural eclogites, are used to calibrate the clinopyroxene-garnet Mg isotope thermometer. This yields a function of Δ26Mgclinopyroxene-garnet = (0.99 ± 0.06) × 106/ T 2, where T is temperature in Kelvin. The refined function not only provides the best empirically calibrated clinopyroxene-garnet Mg isotope thermometer for precise constraints of temperatures of clinopyroxene- and garnet-bearing rocks, but also has potential applications in high-temperature Mg isotope geochemistry.

Germanium enrichment in supergene settings: evidence from the Cristal nonsulfide Zn prospect, Bongará district, northern Peru

NASA Astrophysics Data System (ADS)

Mondillo, Nicola; Arfè, Giuseppe; Herrington, Richard; Boni, Maria; Wilkinson, Clara; Mormone, Angela

2018-02-01

Supergene nonsulfide ores form from the weathering of sulfide mineralization. Given the geochemical affinity of Ge to Si4+ and Fe3+, weathering of Ge-bearing sulfides could potentially lead to Ge enrichments in silicate and Fe-oxy-hydroxide minerals, although bulk rock Ge concentrations in supergene nonsulfide deposits are rarely reported. Here, we present the results of an investigation into Ge concentrations and deportment in the Cristal supergene Zn nonsulfide prospect (Bongará, northern Peru), which formed from the weathering of a preexisting Mississippi Valley-type (MVT) sulfide deposit. Material examined in this study originates from drillcore recovered from oxidized Zn-rich bodies 15-20 m thick, containing 5-45 wt% Zn and Ge concentrations 100 ppm. Microanalysis and laser ablation-ICP-MS show that precursor sphalerite is rich in both Fe (mean Fe = 8.19 wt%) and Ge (mean Ge = 142 ppm). Using the mineral geothermometer GGIMFis—geothermometer for Ga, Ge, In, Mn, and Fe in sphalerite—proposed by Frenzel et al. (Ore Geol Rev 76:52-78, 2016), sphalerite trace element data from the Cristal prospect suggest a possible formation temperature ( T GGIMFis) of 225 ± 50 °C, anomalously high for a MVT deposit. Germanium concentrations measured in both goethite (mean values 100 to 229 ppm, max 511 ppm) and hemimorphite (mean values 39 to 137 ppm, max 258 ppm) are similar to concentrations measured in hypogene sphalerite. Additionally, the Ge concentrations recorded in bulk rock analyses of sphalerite-bearing and oxidized samples are also similar. A persistent warm-humid climate is interpreted for the region, resulting in the development of an oxidation zone favoring the formation of abundant Zn hydrosilicates and Fe hydroxides, both able to incorporate Ge in their crystal structure. In this scenario, Ge has been prevented from dispersion during the weathering of the Ge-bearing sulfide bodies and remains in the resultant nonsulfide ore.

Chemical and mineralogical data and processing methods management system prototype with application to study of the North Caucasus Blybsky Metamorphic Complexes metamorphism PT-condition

NASA Astrophysics Data System (ADS)

Ivanov, Stanislav; Kamzolkin, Vladimir; Konilov, Aleksandr; Aleshin, Igor

2014-05-01

There are many various methods of assessing the conditions of rocks formation based on determining the composition of the constituent minerals. Our objective was to create a universal tool for processing mineral's chemical analysis results and solving geothermobarometry problems by creating a database of existing sensors and providing a user-friendly standard interface. Similar computer assisted tools are based upon large collection of sensors (geothermometers and geobarometers) are known, for example, the project TPF (Konilov A.N., 1999) - text-based sensor collection tool written in PASCAL. The application contained more than 350 different sensors and has been used widely in petrochemical studies (see A.N. Konilov , A.A. Grafchikov, V.I. Fonarev 2010 for review). Our prototype uses the TPF project concept and is designed with modern application development techniques, which allows better flexibility. Main components of the designed system are 3 connected datasets: sensors collection (geothermometers, geobarometers, oxygen geobarometers, etc.), petrochemical data and modeling results. All data is maintained by special management and visualization tools and resides in sql database. System utilities allow user to import and export data in various file formats, edit records and plot graphs. Sensors database contains up to date collections of known methods. New sensors may be added by user. Measured database should be filled in by researcher. User friendly interface allows access to all available data and sensors, automates routine work, reduces the risk of common user mistakes and simplifies information exchange between research groups. We use prototype to evaluate peak pressure during the formation of garnet-amphibolite apoeclogites, gneisses and schists Blybsky metamorphic complex of the Front Range of the Northern Caucasus. In particular, our estimation of formation pressure range (18 ± 4 kbar) agrees on independent research results. The reported study was partially supported by RFBR, research project No. 14-05-00615.

Examination of chloritization of biotite as a tool for reconstructing the physicochemical parameters of mineralization and associated alteration in the Zafarghand porphyry copper system, Ardestan, Central Iran: mineral-chemistry and stable isotope analyses

NASA Astrophysics Data System (ADS)

Aminroayaei Yamini, Maryam; Tutti, Faramarz; Aminoroayaei Yamini, Mohammad Reza; Ahmadian, Jamshid; Wan, Bo

2017-10-01

The chloritization of biotite and stable isotopes of silicate have been studied for the Zafarghand porphyry copper deposit, Ardestan, Iran. The studied area, in the central part of the Urumieh-Dokhtar magmatic belt, contains porphyry-style Cu mineralization and associated hydrothermal alteration within the Miocene (19-26 Ma, Zircon U-Pb age) granodioritc stock and adjacent andesitic to rhyodacitic volcanic rocks (ca. 56 Ma, zircon U-Pb age). The primary and secondary biotite that formed during potassic alteration in this porphyry and these volcanic host rocks are variably chloritized. Chloritization of biotite pseudomorphically is characterized by an increase in MgO, FeOt, and MnO, with decreasing in SiO2, K2O, and TiO2. Based on the Ti-in-biotite geothermometer of Henry et al. (Am Mineral 90:316-328, 2005) and Al-in-chlorite geothermometer of Cathelineau (Clay Miner 23:417-485, 1988), crystallization temperatures of primary biotite representative of magmatic conditions and later chloritization temperature range from 617° to 675 °C ± 24 °C and 177° to 346 °C, respectively. Calculated isotopic compositions of fluids that chloritized primary and secondary biotite display isotopic compositions of 1.1 to 1.7 per mil for δ18O and -19.9 to -20.5 per mil for δD consistent with meteoric water. Sericite, barren, and A-type-quartz veins from phyllic alteration were produced by mixed magmatic and meteoric water with δ18O values from -2.8 to 2.5 and δD values of ˜ -23 per mil; the narrow range of δD values of the propylitic epidote may be due to a meteoric water with δ18O values from 0.8 to 1.6 and δD values from -14.6 to -16.9 per mil.

An empirical NaKCa geothermometer for natural waters

USGS Publications Warehouse

Fournier, R.O.; Truesdell, A.H.

1973-01-01

An empirical method of estimating the last temperature of water-rock interaction has been devised. It is based upon molar Na, K and Ca concentrations in natural waters from temperature environments ranging from 4 to 340??C. The data for most geothermal waters cluster near a straight line when plotted as the function log ( Na K) + ?? log [ ??? (Ca) Na] vs reciprocal of absolute temperature, where ?? is either 1 3 or 4 3 depending upon whether the water equilibrated above or below 100??C. For most waters tested, the method gives better results than the Na K methods suggested by other workers. The ratio Na K should not be used to estimate temperature if ??? ( MCa) MNa is greater than 1. The Na K values of such waters generally yield calculated temperatures much higher than the actual temperature at which water interacted with the rock. A comparison of the composition of boiling hot-spring water with that obtained from a nearby well (170??C) in Yellowstone Park shows that continued water-rock reactions may occur during ascent of water even though that ascent is so rapid that little or no heat is lost to the country rock, i.e. the water cools adiabatically. As a result of such continued reaction, waters which dissolve additional Ca as they ascend from the aquifer to the surface will yield estimated aquifer temperatures that are too low. On the other hand, waters initially having enough Ca to deposit calcium carbonate during ascent may yield estimated aquifer temperatures that are too high if aqueous Na and K are prevented from further reaction with country rock owing to armoring by calcite or silica minerals. The Na-K-Ca geothermometer is of particular interest to those prospecting for geothermal energy. The method also may be of use in interpreting compositions of fluid inclusions. ?? 1973.

Model for origin and evolution of water at volcanoes in São Miguel, Azores (Portugal), based on geochemical and isotopic data set

NASA Astrophysics Data System (ADS)

Woitischek, Julia; Dietzel, Martin; Virgílio Cruz, J.; Inguaggiato, Salvatore; Leis, Albrecht; Böttcher, Michael E.

2016-04-01

A conceptual model is presented to better constrain the origin and evolution of discharges at Sete Cidades, Fogo and Furnas Volcano, using geochemical and isotopic analyses of rock and water as well as recalculated gas composition. The evolution of thermal water clearly reveals that Na-HCO3 and Na-SO4 type of springs have their origin in meteoric water as isotope data are close to the local meteoric water line (δ 18OH2O =-3 ± 1 ‰ V-SMOW; δ DH2O= -13 ± 7 ‰ V-SMOW) with exception of a Na-Cl spring named Ferraria, Sete Cidades area (δ 18OH2O = 0.45 ‰ V-SMOW ; δ DH2O= 4.18 ‰ V-SMOW). Analysed solutions are chemical evolved by evaporation, uptake of volcanic gas, leaching of local basaltic rocks, precipitation of solids, partly admixture of sea water and/or biological activity. Following the individual concentrations supports this model e.g.: HCO3 concentration and the recalculated isotopic composition of gaseous CO2 (δ 13CCO_2 = -4 ± 2.5 ‰ V-PDB) reflect evolved magmatic CO2 uptake and the subsequent leaching progress; High SO42- concentration of up to 16.5 mmol L-1 with δ 34SSO4 = 0.35 ± 0.3 ‰ (V-CDT) reflects magmatic origin which mainly control water chemistry of boiling pools of both Fogo and Furnas lake; δ 18OSO4 = 10.5 ‰ (V-SMOW) suggests organic origin and fits together with the observation of stromatolitic structures in the related precipitates; Molar Mg/Caratio (≈ 0.77) of all thermal discharges reflects leaching of analysed local basalt (Mg/Ca≈ 0.78). Furthermore, shallow and evolved outgassing effects can be distinguished. Equilibrium temperatures for various minerals given in SI vs. T plots and further geothermometers (e.g. Na-K, Na-K-Ca geothermometers) were discussed to estimate temperatures of reservoirs.

The fractionation of nickel between olivine and augite as a geothermometer

USGS Publications Warehouse

Hakli, T.A.; Wright, T.L.

1967-01-01

The coexisting olivine, clinopyroxene and glass of five samples collected from the Makaopuhi lava lake in Hawaii, at temperatures ranging from 1050 to 1160??C were analysed for nickel with an electron probe microanalyser. The results strongly suggest that the distribution of nickel between these three phase pairs well obeys the thermodynamic partition law, and that under favourable conditions, the distribution coefficients permit the estimation of the crystallisation temperature within an accuracy of 10-20??C. It is concluded that the application of the Makaopuhi data to plutonic and to other volcanic rocks should be carried out with caution because the effect of pressure and the changing composition of the phases upon the numerical values of the distribution coefficients is not known quantitatively. ?? 1967.

Favorable Geochemistry from Springs and Wells in Colorado

DOE Data Explorer

Richard E. Zehner

2012-02-01

This layer contains favorable geochemistry for high-temperature geothermal systems, as interpreted by Richard "Rick" Zehner. The data is compiled from the data obtained from the USGS. The original data set combines 15,622 samples collected in the State of Colorado from several sources including 1) the original Geotherm geochemical database, 2) USGS NWIS (National Water Information System), 3) Colorado Geological Survey geothermal sample data, and 4) original samples collected by R. Zehner at various sites during the 2011 field season. These samples are also available in a separate shapefile FlintWaterSamples.shp. Data from all samples were reportedly collected using standard water sampling protocols (filtering through 0.45 micron filter, etc.) Sample information was standardized to ppm (micrograms/liter) in spreadsheet columns. Commonly-used cation and silica geothermometer temperature estimates are included.

Studies of quaternary saline lakes-I. Hydrogen isotope fractionation in saline minerals

USGS Publications Warehouse

Matsuo, S.; Friedman, I.; Smith, G.I.

1972-01-01

Borax, gaylussite, nahcolite and trona were synthesized in aqueous solution at temperatures ranging from 8?? to 35??C. Except for borax, deuterium was always depleted in these hydrated minerals relative to the solutions from which they were crystallized. In borax, no significant fractionation was found. The fractionation factor of D H for the trona-water system exhibited a marked temperature dependence. By combining the deuterium contents of trona and the solution from which trona was crystallized, the following thermometer scale was obtained: In ( D H) trona ( D H)water = 1.420 ?? 104 T2 + 23.56 T (1). An attempt to establish a geothermometer based on C13 C12 fractionation between carbonate minerals and carbonate ions in aqueous solution was not successful. ?? 1972.

The timing and mechanism of depletion in Lewisian granulites

NASA Technical Reports Server (NTRS)

Cohen, A. S.; Onions, R. K.; Ohara, M. J.

1988-01-01

Large Ion Lithophile (LIL) depletion in Lewisian granulites is discussed. Severe depletions in U, Th, and other LIL have been well documented in Lewisan mafic and felsic gneisses, but new Pb isotopic analyses show little or no depletion in lithologies with high solidus temperatures, such as peridotite. This suggests that LIL transport in this terrane took place by removal of partial melts rather than by pervasive flooding with externally derived CO2. The Pb and Nd isotopic data gathered on these rocks show that the depletion and granulite metamorphism are distinct events about 250 Ma apart. Both fluid inclusions and cation exchange geothermometers date from the later metamorphic event and therefore have little bearing on the depletion event, suggesting a note of caution for interpretations of other granulite terranes.

Pyroxene-melt equilibria. [for lunar maria basalts

NASA Technical Reports Server (NTRS)

Nielsen, R. L.; Drake, M. J.

1979-01-01

A thermodynamic analysis of pyroxene-melt equilibria is performed through use of a literature survey of analyses of high-Ca pyroxene and coexisting silicate melt pairs and analyses of low-Ca pyroxene silicate melt pairs. Reference is made to a modified version of a model developed by Bottinga and Weill (1972) which more successfully accounts for variations in melt composition than does a model which considers the melt to be composed of simple oxides which mix ideally. By using a variety of pyroxene melt relations, several pyroxene-melt and low-Ca pyroxene-high-Ca pyroxene geothermometers are developed which have internally consistant precisions of approximately + or - 20 C. Finally, it is noted that these equations may have application in modeling the evolution of mineral compositions during differentiation of basaltic magmas.

Geochemical study of the Sakalol-Harralol geothermal field (Republic of Djibouti): Evidences of a low enthalpy aquifer between Manda-Inakir and Asal rift settings

NASA Astrophysics Data System (ADS)

Awaleh, Mohamed Osman; Boschetti, Tiziano; Soubaneh, Youssouf Djibril; Baudron, Paul; Kawalieh, Ali Dirir; Dabar, Omar Assowe; Ahmed, Moussa Mahdi; Ahmed, Samaleh Idriss; Daoud, Mohamed Ahmed; Egueh, Nima Moussa; Mohamed, Jalludin

2017-02-01

Eighty-six sodium bicarbonate to sodium chloride hot springs and four water wells in the Tadjourah Region of Djibouti were investigated for major, minor (B, Br, F, Sr, Li) chemistry and isotope composition of water and dissolved components (87Sr/86Sr, 11B/10B, 13C/12C and 14C of DIC, 34S/32S and 18O/16O of sulfate). The deep saline Na-Cl reservoir at 143 °C shows affinity with the shallow geothermal water from the "active" Asal rift. Asal water is a diluted and recycled seawater component with the major cation composition obliterated by equilibration with Stratoid basalt. Locally, the deep reservoir is differentiated in term of recharge, and re-equilibration with rocks and mixing. In particular, two spring groups reveal contributions from evaporites typical of the "passive" graben setting of the Afar. A model on 34S/32S and 18O/16O demonstrates the isotope imprint of magmatic SO2 disproportionation on dissolved and solid sulfate, whose values probably persists in a sedimentary environment without trace of seawater. On the other hand a seawater signature, modified by mixing and secondary fractionation effects, is partially maintained according to the boron isotope composition (up to + 27.4‰). Temperature estimation in low-enthalpy geothermal reservoirs is notoriously difficult, especially where mixing with fluids of differing genesis and/or conduction cooling take place. From a geothermometric point of view, the multi-method approach followed in this study (up-to-date theoretical and thermodynamic equations, ad-hoc silica geothermometers inferred from local rocks, checking of the results on a 18Oαsulfate-water vs. temperature diagram) provides some insights and perspectives on how to tackle the problem. Table S2. Sampling locations, T, pH, EC, TDS and hydrochemical types of the sampled waters. Table S3. Chemical analyses of thermal and cold waters from Sakalaol-Haralol geothermal field. Table S4. Mineral saturation indices of SHGF hot springs waters calculated at the sampling conditions. Table S5. Geothermometric estimations of the SHGF deep temperature calculated fromthe hot springwater samples. All displayed values are in °C. In the chemical geothermometer equations, aqueous silica (SiO2), Na and K concentration in ppm were used, whereas δ18O(SO4) and δ18O(H2O) values were used in the isotope geothermometer equations. Table S6. 14C age models. Fig. S1. Hierarchical cluster analysis (The pink line is "phenon line"). Fig. S2. Principal Component analysis results. Fig. S3. (1) Diagram showing the change in calculated saturation indices (Log(Q/K)) of carbonate minerals as a function of temperature for C1 thermal waters. (2) Diagram showing the change in calculated saturation indices (Log(Q/K)) of carbonate minerals as a function of temperature for C2 thermal waters. (3) Diagram showing the change in calculated saturation indices (Log(Q/K)) of carbonate minerals as a function of temperature for C3 thermal waters. (4) Diagram showing the change in calculated saturation indices (Log(Q/K)) of carbonate minerals as a function of temperature for C4 thermal waters (sample # 90). Fig. S4. Regional piezometric map adapted from the country piezomztric map (BGR, 1982).

A geochemical reconnaissance of the Alid volcanic center and geothermal system, Danakil depression, Eritrea

USGS Publications Warehouse

Lowenstern, J. B.; Janik, C.J.; Fournier, R.O.; Tesfai, T.; Duffield, W.A.; Clynne, M.A.; Smith, James G.; Woldegiorgis, L.; Weldemariam, K.; Kahsai, G.

1999-01-01

Geological and geochemical studies indicate that a high-temperature geothermal system underlies the Alid volcanic center in the northern Danakil depression of Eritrea. Alid is a very late-Pleistocene structural dome formed by shallow intrusion of rhyolitic magma, some of which vented as lavas and pyroclastic flows. Fumaroles and boiling pools distributed widely over an area of ~10 km2 on the northern half of Alid suggest that an active hydrothermal system underlies much of that part of the mountain. Geothermometers indicate that the fumarolic gases are derived from a geothermal system with temperatures >225??C. The isotopic composition of condensed fumarolic steam is consistent with these temperatures and implies that the source water is derived primarily from either lowland meteoric waters or fossil Red Sea water, or both. Some gases vented from the system (CO2, H2S and He) are largely magmatic in origin. Permeability beneath the volcanic center may be high, given the amount of intrusion-related deformation and the active normal faulting within the Danakil depression.Geological and geochemical studies indicate that a high-temperature geothermal system underlies the Alid volcanic center in the northern Danakil depression of Eritrea. Alid is a very late-Pleistocene structural dome formed by shallow intrusion of rhyolitic magma, some of which vented as lavas and pyroclastic flows. Fumaroles and boiling pools distributed widely over an area of approx. 10 km2 on the northern half of Alid suggest that an active hydrothermal system underlies much of that part of the mountain. Geothermometers indicate that the fumarolic gases are derived from a geothermal system with temperatures >225??C. The isotopic composition of condensed fumarolic steam is consistent with these temperatures and implies that the source water is derived primarily from either lowland meteoric waters or fossil Red Sea water, or both. Some gases vented from the system (CO2, H2S and He) are largely magmatic in origin. Permeability beneath the volcanic center may be high, given the amount of intrusion-related deformation and the active normal faulting within the Danakil depression.

The Hydrogeochemistry of Qingshui Geothermal Field, Northeastern Taiwan.

NASA Astrophysics Data System (ADS)

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 earth elements (REEs) were also measured in this study. The results normalized by North America Shale REEs (NASC) show a flat pattern and a distinct europium positive anomaly. It possibly indicates a chemical interaction between meteoric water and sedimentary rock, which excludes the possibility of an igneous source.

Isotopic and chemical composition of parbati valley geothermal discharges, North-West Himalaya, India

USGS Publications Warehouse

Giggenbach, W.F.; Gonfiantini, R.; Jangi, B.L.; Truesdell, A.H.

1983-01-01

The isotopic compositions of the waters discharged from Parbati Valley geothermal areas indicate a higher altitude meteoric origin, with discharge temperatures reflecting variations in the depth of penetration of the waters to levels heated by the existence of a 'normal' geothermal gradient. On the basis of mixing models involving silica, tritium, discharge temperatures and chloride contents, deep equilibration temperatures of 120-140??C were obtained for Manikaran, possibly reaching 160??C at even greater depth. Geothermometers based on sulfate-water 18O exchange and gas reactions point to similar temperatures. Exceptionally high helium contents of the discharges correspond to apparent crustal residence times of the waters in the order of 10-100 Ma; relative nitrogen-argon contents support a largely meteoric origin of the waters with a possible fossil brine, but no detectable magmatic component. ?? 1983.

Electron Spin Resonance (ESR) Studies of Returned Comet Nucleus Samples

NASA Technical Reports Server (NTRS)

Tsay, Fun-Dow; Kim, Soon Sam; Liang, Ranty H.

1997-01-01

Electron Spin Resonance (ESR) studies have been carried out on organic and inorganic free radicals generated by gamma-ray and/or UV-irradiation and trapped in ice matrices. It is suggested that the concentration of these free radicals together with their thermal stability can be used as an accurate built-in geothermometer and radiation probe for returned comet nucleus sample studies. ESR studies have also been carried out on paramagnetic (Mn(2+), Ti(3+), and Fe(3+)) and ferromagnetic (ferric oxide and metallic iron) centers known to be present in terrestrial and extraterrestrial samples. The presence or absence of these magnetic centers coupled with their characteristic ESR lineshape can be used to investigate the shock effects, quenching/cooling rate and oxidation-reduction conditions in the formation and subsequent evolution of returned comet nucleus samples.

Application of graphite as a geothermometer in hydrothermally altered metamorphic rocks of the Merelani-Lelatema area, Mozambique Belt, northeastern Tanzania

NASA Astrophysics Data System (ADS)

Malisa, Elias Pausen

1998-02-01

Upper Precambrian pelitic and psammitic gneisses in the Mozambique Belt are usually graphite rich. The determination of crystallisation temperatures around and in the hydrothermally altered rocks of the Merelani-Lelatema mining areas, northeastern Tanzania, were made by studying the lattice parameter C of graphite. In this way, the migration of the chromophore elements giving colour to the gemstones, e.g. tanzanite, green garnet and green tourmaline in the area, can be studied. Within the hydrothermally altered zone graphite gives temperatures that range from 523°C to 880°C. These temperatures are much higher than the 390-440°C obtained through fluid inclusion studies of tanzanite, which indicates that the graphite was not hydrothermally introduced. Furthermore the hydrothermal solutions are post-metamorphic.

DOE Office of Scientific and Technical Information (OSTI.GOV)

Spycher, Nicolas; Peiffer, Loic; Finsterle, Stefan

GeoT implements the multicomponent geothermometry method developed by Reed and Spycher (1984, Geochim. Cosmichim. Acta 46 513–528) into a stand-alone computer program, to ease the application of this method and to improve the prediction of geothermal reservoir temperatures using full and integrated chemical analyses of geothermal fluids. Reservoir temperatures are estimated from statistical analyses of mineral saturation indices computed as a function of temperature. The reconstruction of the deep geothermal fluid compositions, and geothermometry computations, are all implemented into the same computer program, allowing unknown or poorly constrained input parameters to be estimated by numerical optimization using existing parameter estimationmore » software, such as iTOUGH2, PEST, or UCODE. This integrated geothermometry approach presents advantages over classical geothermometers for fluids that have not fully equilibrated with reservoir minerals and/or that have been subject to processes such as dilution and gas loss.« less

Gas Geochemistry of the Dogger Geothermal Aquifer (Paris Basin, France)

DOE Office of Scientific and Technical Information (OSTI.GOV)

Criaud, A.; Fouillac, C.; Marty, B.

1987-01-20

The low enthalpy program developed in the Paris Basin provides the opportunity for studying the gas geochemistry of the calcareous aquifer of the Dogger. Hydrocarbons and CO{sub 2} are mainly biogenic, He displays high concentrations. He, Ar and N{sub 2} have multiple origins (radioactive decay, atmospheric migration, biochemical processes). The distribution of the gases in the zones of the basin varies in relation to the general chemistry, sedimentology and hydrodynamics. The gas geothermometers do not apply to this environment but useful estimations of the redox potential of the fluid can be derived from CO{sub 2}/CH{sub 4} and N{sub 2}/NH{sub 4}{supmore » +} ratios. H{sub 2} and H{sub 2}S are involved in corrosion processes and scaling in the pipes. 12 refs., 3 figs., 2 tabs.« less

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

USGS Publications Warehouse

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

Isotopic studies of epigenetic features in metalliferous sediment, Atlantis II Deep, Red Sea

USGS Publications Warehouse

Zierenberg, Robert A.; Shanks, Wayne C.

1988-01-01

The unique depositional environment of the Atlantis II Deep brine pool in the Red Sea produces a stratiform metalliferous deposit of greater areal extent than deposits formed by buoyant-plume systems typical of the midocean ridges because of much more efficient metal entrapment. Isotopic analyses of strontium, sulfur, carbon, and oxygen from the metalliferous sediments indicate that three major sources contribute dissolved components to the hydrothermal system: seawater, Miocene evaporites, and rift-zone basalt. An areally restricted magnetite-hematite-pyroxene assemblage formed at high temperatures, possibly in response to hydrothermal convection initiated by intrusion of basalt into the metalliferous sediment. A correlation between smectite Fe/(Fe+Mg) ratios and oxygen isotope temperatures suggests that smectite is a potentially important chemical geothermometer, and confirms geochemical calculations indicating that Mg-rich smectite is more stable than Fe-rich smectite at elevated temperatures.

Improved Geothermometry Through Multivariate Reaction-path Modeling and Evaluation of Geomicrobiological Influences on Geochemical Temperature Indicators: Final Report

DOE Office of Scientific and Technical Information (OSTI.GOV)

Mattson, Earl; Smith, Robert; Fujita, Yoshiko

2015-03-01

The project was aimed at demonstrating that the geothermometric predictions can be improved through the application of multi-element reaction path modeling that accounts for lithologic and tectonic settings, while also accounting for biological influences on geochemical temperature indicators. The limited utilization of chemical signatures by individual traditional geothermometer in the development of reservoir temperature estimates may have been constraining their reliability for evaluation of potential geothermal resources. This project, however, was intended to build a geothermometry tool which can integrate multi-component reaction path modeling with process-optimization capability that can be applied to dilute, low-temperature water samples to consistently predict reservoirmore » temperature within ±30 °C. The project was also intended to evaluate the extent to which microbiological processes can modulate the geochemical signals in some thermal waters and influence the geothermometric predictions.« less

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

NASA Astrophysics Data System (ADS)

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.

Untangling the History of Oceanic Peridotites Using Spinel Oxybarometry

NASA Astrophysics Data System (ADS)

Birner, S.; Warren, J. M.; Cottrell, E.; Davis, F. A.

2014-12-01

Comprehensive knowledge of the oxygen fugacity of the upper mantle is critical to understanding the processes associated with melt production, interaction, and extraction. Thus, it is important to understand how fO2 changes during a peridotite's thermal and petrologic history in the asthenospheric and lithospheric mantle, as metamorphic subsolidus reequilibration can result in changes to recorded fO2. A case study of Tongan forearc peridotites highlights the heterogeneity seen in mantle peridotites. We analyzed two dredges located 250 km apart along the trench: one dredge ranges in fO2 from 0.5 to 1 log unit above the QFM buffer, similar to analyses of supra-subduction zone xenoliths (e.g. Brandon and Draper, 1996; Wood and Virgo, 1989) while the other dredge ranges from QFM-0.75 to QFM+0.25 and exhibits high spinel Cr# (ranging from 0.45 to 0.75). Systematics between fO2, Ti concentration, olivine forsterite content, and Cr# within each dredge allow us to differentiate between the effects of melt extraction, melt interaction, and cooling. Because the spinel oxybarometry equation is dependent on temperature, it is important to be able to accurately determine the temperature recorded by peridotites. Though many geothermometers are available for mantle rocks, we assert that geothermometers based on Fe-Mg exchange between olivine and spinel are the most applicable to fO2 calculations, because the oxygen fugacity recorded by a mantle assemblage is primarily controlled by this exchange. Additionally, preliminary analyses of diffusion profiles across olivine-spinel grain boundaries provide insight into the cooling of peridotite in the oceanic lithosphere and its effects on oxygen fugacity. Mg-Fe exchange between olivine and spinel is controlled by the distribution coefficient, KD, which is dependent on both temperature and the proportion of Cr to other trivalent cations in spinel. We see an increase in olivine forsterite content towards the olivine-spinel interface, consistent with an increase in KD as cooling occurs. Limited data indicate that while spinel Cr# decreases as the interface is approached, no change is seen in spinel Fe3+/ΣFe ratios. As a result, the increased Fo# in olivine dominates the oxybarometry equation, resulting in higher oxygen fugacity values near the interface as cooling occurs.

Organic matter and metamorphic history of CO chondrites

NASA Astrophysics Data System (ADS)

Bonal, Lydie; Bourot-Denise, Michèle; Quirico, Eric; Montagnac, Gilles; Lewin, Eric

2007-03-01

The metamorphic grades of a series of eight CO3 chondrites (ALHA77307, Colony, Kainsaz, Felix, Lancé, Ornans, Warrenton and Isna) have been quantified. The method used was based on the structural grade of the organic matter trapped in the matrix, which is irreversibly transformed by thermal metamorphism. The maturation of the organic matter is independent with respect to the mineralogical context and aqueous alteration. This metamorphic tracer is thus valid whatever the chemical class of chondrites. Moreover, it is sensitive to the peak metamorphic temperature. The structural grade of the organic matter was used along with other metamorphic tracers such as petrography of opaque minerals, Fa and Fs silicate composition in type I chondrules, presolar grains and noble gas (P3 component) abundance. The deduced metamorphic hierarchy and the attributed petrographic types are the following: ALHA77307 (3.03) < Colony (3.1) < Kainsaz (3.6) < Felix (3.6 (1)) < Ornans (3.6 (2)) < Lancé (3.6 (3)) < Warrenton (3.7 (1)) < Isna (3.7 (2)). For most metamorphosed objects, the peak metamorphic temperature can be estimated using a geothermometer calibrated with terrestrial metasediments [Beyssac O., Goffe B., Chopin C., and Rouzaud J. N. (2002) Raman spectrum of carbonaceous material in metasediments: a new geothermometer. J. Metamorph. Geol., 20, 859-871]. A value of 330 °C was obtained for Allende (CV chondrite), Warrenton and Isna, consistent with temperatures estimated from Fe diffusion [Weinbruch S., Armstrong J., and Palme H. (1994). Constraints on the thermal history of the Allende parent body as derive from olivine-spinel thermometry and Fe/Mg interdiffusion in olivine. Geochim. Cosmochim. Acta58(2), 1019-1030.], from the Ni content in sulfide-metal assemblages [Zanda B., Bourot-Denise M., and Hewins R. (1995) Condensate sulfide and its metamorphic transformations in primitive chondrites. Meteorit. Planet. Sci.30, A605.] and from the d002 interlayer spacing in poorly graphitized carbon [Rietmeijer, F., and MacKinnon, I. (1985) Poorly graphitized carbon as a new cosmothermometer for primitive extraterrestrial materials. Nature, 315, 733-736]. The trapped noble gas and C content appear to be sensitive but not precise metamorphic tracers, indicating that the "Ornans paradox" does not exist. Major problems with the current petrologic types derived from Induced ThermoLuminescence are pointed out.

Raman spectral characteristics of magmatic-contact metamorphic coals from Huainan Coalfield, China

NASA Astrophysics Data System (ADS)

Chen, Shancheng; Wu, Dun; Liu, Guijian; Sun, Ruoyu

2017-01-01

Normal burial metamorphism of coal superimposed by magmatic-contact metamorphism makes the characteristics of the Raman spectrum of coal changed. Nine coal samples were chosen at a coal transect perpendicular to the intrusive dike, at the No. 3 coal seam, Zhuji Coal Mine, Huainan Coalfield, China, with different distances from dike-coal boundary (DCB). Geochemical (proximate and ultimate) analysis and mean random vitrinite reflectance (R0, %) indicate that there is a significant relationship between the values of volatile matter and R0 in metamorphosed coals. Raman spectra show that the graphite band (G band) becomes the major band but the disordered band (D band) disappears progressively, with the increase of metamorphic temperature in coals, showing that the structural organization in high-rank contact-metamorphosed coals is close to that of well-crystallized graphite. Evident relationships are observed between the calculated Raman spectral parameters and the peak metamorphic temperature, suggesting some spectral parameters have the potentials to be used as geothermometers for contact-metamorphic coals.

Preliminary evaluation of thermal and nonthermal waters at selected sites in Panama, Central America. Evaluacion preliminar de aguas termales y no termales de sitios seleccionados en Panama, Centroamerica

DOE Office of Scientific and Technical Information (OSTI.GOV)

Shevenell, L.

1989-11-01

Thirty-one thermal and nonthermal water samples were collected in Panama by the Instituto de Recursos Hidraulicos y Electrificacion and analyzed by the Earth and Space Sciences Division at Los Alamos National Laboratory to evaluate the geothermal potential of four different areas. Chemical and isotopic analyses were performed on each sample. Because samples from several areas were submitted, the chemistry of the samples is varied, with total dissolved solids of thermal fluids ranging from 900 to nearly 10,000 mg/{ell}. All water samples studied are meteoric in origin, and none of the thermal waters exhibit an {sup 18}O enrichment, which is characteristicmore » of high-temperature isotopic, exchange between water and rock. At all four areas, calculated geothermometer temperatures within a reservoir of less than 160{degrees}C. 4 refs., 4 figs., 6 tabs.« less

Chemical and isotopic prediction of aquifer temperatures in the geothermal system at Long Valley, California

USGS Publications Warehouse

Fournier, R.O.; Sorey, M.L.; Mariner, R.H.; Truesdell, A.H.

1979-01-01

Temperatures of aquifers feeding thermal springs and wells in Long Valley, California, estimated using silica and Na-K-Ca geothermometers and warm spring mixing models, range from 160/dg to about 220??C. This information was used to construct a diagram showing enthalpy-chloride relations for the various thermal waters in the Long Valley region. The enthalpy-chloride information suggests that a 282 ?? 10??C aquifer with water containing about 375 mg chloride per kilogram of water is present somewhere deep in the system. That deep water would be related to ??? 220??C Casa Diablo water by mixing with cold water, and to Hot Creek water by first boiling with steam loss and then mixing with cold water. Oxygen and deuterium isotopic data are consistent with that interpretation. An aquifer at 282??C with 375 mg/kg chloride implies a convective heat flow in Long Valley of 6.6 ?? 107 cal/s. ?? 1979.

A Review of Methods Applied by the U.S. Geological Survey in the Assessment of Identified Geothermal Resources

USGS Publications Warehouse

Williams, Colin F.; Reed, Marshall J.; Mariner, Robert H.

2008-01-01

The U. S. Geological Survey (USGS) is conducting an updated assessment of geothermal resources in the United States. The primary method applied in assessments of identified geothermal systems by the USGS and other organizations is the volume method, in which the recoverable heat is estimated from the thermal energy available in a reservoir. An important focus in the assessment project is on the development of geothermal resource models consistent with the production histories and observed characteristics of exploited geothermal fields. The new assessment will incorporate some changes in the models for temperature and depth ranges for electric power production, preferred chemical geothermometers for estimates of reservoir temperatures, estimates of reservoir volumes, and geothermal energy recovery factors. Monte Carlo simulations are used to characterize uncertainties in the estimates of electric power generation. These new models for the recovery of heat from heterogeneous, fractured reservoirs provide a physically realistic basis for evaluating the production potential of natural geothermal reservoirs.

Oxygen isotope fractionation between analcime and water - An experimental study

NASA Technical Reports Server (NTRS)

Karlsson, Haraldur R.; Clayton, Robert N.

1990-01-01

The oxygen isotope fractionation between analcime and water is studied to test the feasibility of using zeolites as low-temperature thermometers. The fractionation of oxygen isotopes between natural analcime and water is determined at 300, 350, and 400 C, and at fluid pressures ranging from 1.5 to 5.0 kbar. Also, isotope ratios for the analcime framework, the channel water, and bulk water are obtained. The results suggest that the channel water is depleted in O-18 relative to bulk water by a constant value of about 5 percent, nearly independent of temperature. The analcime-water fractionation curve is presented, showing that the exchange has little effect on grain morphology and does not involve recrystallization. The exchange is faster than any other observed for a silicate. The exchange rates suggest that zeolites in active high-temperature geothermal areas are in oxygen isotopic equilibrium with ambient fluids. It is concluded that calibrated zeolites may be excellent low-temperature oxygen isotope geothermometers.

Investigating Volcanic-Hydrothermal Systems in Dominica, Lesser Antilles: Temporal Changes in the Chemical Composition of Hydrothermal Fluids for Volcanic Monitoring Using Geothermometers

NASA Astrophysics Data System (ADS)

Onyeali, M. M. C.; Joseph, E. P.; Frey, H. M.

2017-12-01

Dominica has an abundance of volcanic activity, with nine potentially active volcanoes, many of which have highly active volcanic-hydrothermal systems. The waters are predominantly acid-sulphate in character (SO4=100-4200 mg/L, pH≤4), and likely formed because of dilution of acidic gases in near surface oxygenated groundwater. The waters are of primarily meteoric origin, but are likely affected by evaporation effects at/near the surface, with δ18O ranging from -1.75 to 10.67‰, and δD from -6.1 to 14.5‰. With updated water chemistry and isotopic data from five hydrothermal areas (Boiling Lake, Valley of Desolation, Sulphur Springs, Wotten Waven, Cold Soufriere) for the period 2014 to 2017, we will re-evaluate the characteristics of these systems, which were last reported in 2011. We will present updated reservoir temperatures using a variety of geothermometers and provide insight into water-rock interactions taking place in the reservoirs. Recent changes in chemistry of the waters have indicated that while the origin of the hydrothermal systems are still dominantly meteoric (δ18O = -3 to 8‰ and δD = -5 to 18‰), surface evaporation effects and variable amounts of mixing with shallow ground waters play an important role. Fumaroles appear to reflect a deeper source contribution as compared to thermal waters with differences in acidity, temperature, TDS, δ18O, and δD observed. The general composition of the waters for most of the hydrothermal systems studied indicate no significant changes, with the exception of the Boiling Lake, which experienced a draining event in November 2016 which lasted for 6 weeks. Decreases in temperature, pH, Na, K, and Cl were seen post draining, while SO4 remained relatively low (66 ppm), but showed a small increase. The chemistry of the Boiling Lake appears to show significant changes in response to changes in the groundwater system. Changes in the groundwater system at the lake observed during the 2004/2005 draining, which lasted for 6 months, were attributed to strain release from a nearby regional seismic event. Based on the changes observed during the recent draining events, there are likely other factors affecting the ground water system at the Boiling Lake. Of particular note is the drastic change in SO4 concentrations in the Boiling Lake, which went from 1830 ppm in 2003 to <100 ppm presently.

Subsurface temperatures and surface heat flow in the Michigan Basin and their relationships to regional subsurface fluid movement

USGS Publications Warehouse

Vugrinovich, R.

1989-01-01

Linear regression of 405 bottomhole temperature (BHT) measurements vs. associated depths from Michigan's Lower Peninsula results in the following equation relating BHT and depth: BHT(??C) = 14.5 + 0.0192 ?? depth(m) Temperature residuals, defined as (BHT measured)-(BHT calculated), were determined for each of the 405 BHT's. Areas of positive temperature residuals correspond to areas of regional groundwater discharge (determined from maps of equipotential surface) while areas of negative temperature residuals correspond to areas of regional groundwater recharge. These relationships are observed in the principal aquifers in rocks of Devonian and Ordovician age and in a portion of the principal aquifer in rocks of Silurian age. There is a similar correspondence between high surface heat flow (determined using the silica geothermometer) and regional groundwater discharge areas and low surface heat flow and regional groundwater recharge areas. Post-Jurassic depositional and tectonic histories suggest that the observed coupling of subsurface temperature and groundwater flow systems may have persisted since Jurassic time. Thus the higher subsurface palaeotemperatures (and palaeogeothermal gradients) indicated by recent studies most likely pre-date the Jurassic. ?? 1989.

Analysis geothermal prospect of Mt. Endut using geochemistry methods

NASA Astrophysics Data System (ADS)

Sobirin, R.; Permadi, A. N.; Akbar, A. M.; Wildan, D.; Supriyanto

2017-07-01

Mt. Endut geothermal area is located in Lebak district, Banten province, about 40 km to the south of the town of Rangkasbitung. There are four manifestations of hot springs i.e: Handeuleum hot springs, Cikawah 1, Cikawah 2, and Gajrug. Based on geochemical analysis using Na-K-Mg triangular diagrams, Cl-Li-B, and Cl-SO4-HCO3, it is known that Cikawah 1 hot springs is chloride type and the other springs are bicarbonate type. Reservoir temperature range is from 162°C to 180°C are predicted by SiO2 and NaK geothermometers. In general all hot springs are out flows, but there is an hypothesis that Cikawah 1 is the up flow. Because it is in partial equilibrium and chloride type. Mount Endut has a hydrothermal system with a fluid reservoir in the form of hot water or water dominated system. The geothermal prospect area of Mount Endut is located around the Cikawah manifestation to the western part of the Endut mountain. Further research is required by conducting geophysical surveys around the Mount Endut.

NaSi⇌CaAl exchange equilibrium between plagioclase and amphibole

NASA Astrophysics Data System (ADS)

Spear, Frank S.

1980-03-01

The exchange equilibrium between plagioclase and amphibole, 2 albite+tschermakite=2 anorthite+glaucophane, has been calibrated empirically using data from natural amphibolites. The partition coefficient, K D, for the exchange reaction is ( X an/ X ab)plag ·(Na, M4/Ca, M4)amph.. Partitioning is systematic between plagioclase and amphibole in suites collected from single exposures, but the solid solutions are highly non-ideal: values of In K D range from -3.0 at X an=0.30 to -1.0 at X an=0.90 in samples from a single roadcut. Changes in both K D and the topology of the ternary reciprocal exchange diagram occur with increasing metamorphic grade. Temperature dependence of In K D is moderate with Δ ¯H≃35 to 47 kcal at X an=0.25; pressure dependence is small with Δ ¯V≃ -0.24 cal/bar. Usefulness of this exchange equilibrium as a geothermometer is restricted by uncertainties in the calculation of the amphibole formula from a microprobe analysis, especially with regard to Na, M4 in amphibole, to approximately ±50 ° C.

Geochemistry of hot springs in the Ie Seu’um hydrothermal areas at Aceh Besar district, Indonesia

NASA Astrophysics Data System (ADS)

Idroes, R.; Yusuf, M.; Alatas, M.; Subhan; Lala, A.; Saiful; Suhendra, R.; Idroes, G. M.; Marwan

2018-03-01

Indonesia geothermal resources are the largest in the world, about 40 percent of the total geothermal resources worldwide with a potential energy of 28,617 MW. Geothermal energy is one of the renewable energy in the world that can be developed sustainably. This kind of energy is not only environmentally friendly but also highly prospective compared to fossil energy. One of the potential geothermal energy in Indonesia is Seulawah Agam geothermal field with some manifestation areas. The fluid type of Ie Seu’um manifestation was chloride (Cl-) obtained from the ternary diagram Cl--SO4 2--HCO3 -, using UV-Vis spectrophotometry, argentometry and acidimetry method. The reservoir range temperature was 188,7 ± 9,3°C calculated using geothermometer Na-K-Ca, Na-K Fournier and Na-K Giggenbach by applying Atomic Absorption Spectroscopy method. This data processing was carried out using liquid chemistry plotting spreadsheet version 3 powell geoscience Ltd.3 September 2012 by Powell & Cumming. The potential in the geothermal manifestation of Ie Seu’um was estimated about 50-100 MW (medium enthalpy).

Implications for organic maturation studies of evidence of a geologically rapid increase and stabilization of vitrinite reflectance at peak temperature: Cerro Prieto geothermal system, Mexico

USGS Publications Warehouse

Barker, C.E.

1991-01-01

A short-term rapid heating and cooling of the rock in well M-94 below 1300 m was caused by a pulse of hot water passing through the edge of the Cerro Prieto, Mexico, geothermal system. Below 1300 m, the peak paleotemperatures were about 225-250??C, but equilibrium well log temperatures indicate a decrease to 150-210??C at present. This hot water pulse sharply increased vitrinite reflectance to levels comparable to those measured in the central part of the system, even though studies of apatite fission-track annealing indicate that the duration of heating was only 100-101 yr in M-94, in contrast to 103-104 yr in the central part of the system. The quick change of the vitrinite reflectance geothermometer indicates that thermal maturation reactions can stabilize, after a geologically short period of heating, to a level consistent with peak temperature under moderate to high-temperature diagenesis in open, fluid-rich, geothermal systems. -from Author

Assessment of the origin and geothermal potential of the thermal waters by hydro-isotope geochemistry: Eskisehir province, Turkey.

PubMed

Yuce, Galip; Italiano, Francesco; Yasin, Didem; Taskiran, Lutfi; Gulbay, Ahmet Hilmi

2017-05-01

The thermal fluids vented over Eskisehir province have been investigated for their origin and to estimate the geothermal potential of the area. Thermal waters as well as bubbling and dissolved gases were collected and analysed for their chemical and isotopic features. Their isotopic composition varies in the range from -11.5 to -7.7 ‰ for δ 18 O, -84 and -57 ‰ for δ 2 H, and 0-7.2 TU for tritium. The gases (bubbling and dissolved) are mostly N 2 -dominated with a significant amount of CO 2 . The helium isotopic ratios are in the range of 0.2-0.66 R/Rac, indicate remarkable mantle-He contribution ranging between 2 and 10 % in the whole study area. Considering the estimated geothermal gradient about three times higher than the normal gradient, and the reservoir temperatures estimated to be between 50 and 100 °C using quartz and chalcedony geothermometers, a circulation model was built where possible mixing with shallow waters cool down the uprising geothermal fluids.

Fe-Ti oxide geothermometry: thermodynamic formulation and the estimation of intensive variables in silicic magmas

NASA Astrophysics Data System (ADS)

Ghiorso, Mark S.; Sack, O.

1991-10-01

A new thermodynamic formulation of the Fe-Ti oxide geothermometer/oxygen barometer is developed. The method is based upon recently calibrated models for spinel solid solutions in the quinary system (Fe2+, Mg)(Al,Fe3+,Cr)2O4-(Fe2+, Mg)2TiO4 by Sack and Ghiorso, and rhombohedral oxides in the quaternary system (Fe2+,Mg,Mn)TiO3-Fe2O3 (this paper). The formulation is internally consistent with thermodynamic models for (Fe2+,Mg)-olivine and -orthopyroxene solid solutions and end-member thermodynamic properties tabulated by Berman. The constituent expressions account for compositional and temperature dependent cation ordering and reproduce miscibility gap features in all of the component binaries. The calibration does not account for the excess Gibbs energy resulting from compositional and temperature dependent magnetic ordering in either phase. This limits application of the method to assemblages that equilibrated at temperatures above 600° C. Practical implementation of the proposed geothermometer/oxygen barometer requires minimal use of projection algorthms in accommodating compositions of naturally occurring phases. The new formulation is applied to the estimation of temperature and oxygen fugacity in a wide variety of intermediate to silicic volcanic rocks. In combination with previous work on olivine and orthopyroxene thermodynamics, equilibration pressures are computed for a subset of these volcanics that contain the assemblage quartz, oxides and either ferromagnesian silicate. The calculated log10 f O 2- T relations are reflected in coexisting ferromagnesian mineral assemblages. Volcanics with the lowest relative oxygen fugacity (Δlog10 f O 2) are characterized by the assemblage olivine-quartz, those with slightly higher Δ log10 f O 2 s, by the assemblage orthopyroxene-quartz. The sequence proceeds with the necessary phases biotite-feldspar, then hornblende-quartz-clinopyroxene, and finally at the highest Δ log10 f O 2 s, sphene-quartz-clinopyroxene. Quantitative analysis of these trends, utilizing thermodynamic data for the constituent phases, establishes that, in most cases, the T-log10 f O 2value computed from the oxides is consistent with the compositions of coexisting silicate phases, indicating that phenocryst equilibrium was achieved prior to eruption. There is, however, considerable evidence of oxide-silicate disequilibrium in samples collected from more slowly cooled domes and obsidians. In addition, T-log10 f O 2trends from volcanic rocks that contain biotite and orthopyroxene are interpreted to imply a condition of Fe2+-Mg exchange disequilibrium between orthopyroxene and coexisting ferromagnesian silicates and melt. It is suspected that many biotite-feldspar-quartz-orthopyroxene bearing low temperature volcanic rocks inherit orthopyroxene xenocrysts which crystallized earlier in the cooling history of the magma body.

Infrared Spectroscopy for Rapid Characterization of Drill Core and Cutting Mineralogy

NASA Astrophysics Data System (ADS)

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

2009-12-01

Water geochemistry can vary with depth and location within a geothermal reservoir, owing to natural factors such as changing rock type, gas content, fluid source and temperature. The interaction of these variable fluids with the host rock will cause well known changes in alteration mineral assemblages that are commonly factored into the exploration of hydrothermal systems for economic metals, but are less utilized with regard to mapping borehole geology for geothermal energy production. Chemistry of geothermal fluids and rock alteration products can impact production factors such as pipeline corrosion and scaling and early studies explored the use of both silica and chlorites as geothermometers. Infrared spectroscopy is particularly good at identifying a wide variety of alteration minerals, especially in discrimination among clay minerals, with no sample preparation. The technique has been extensively used in the remote identification of materials, but is not commonly used on drill core or chips. We have performed several promising pilot studies that suggest the power of the technique to sample continuously and provide mineral logs akin to geophysical ones. We have surveyed a variety of samples, including drill chip boards, boxed core, and drill cuttings from envelopes, sample bottles and chip trays. This work has demonstrated that core and drill chips can be rapidly surveyed, acquiring spectra every few to tens of cm of section, or the vertical resolution of the chip tray (typically 10 feet). Depending on the sample type we can acquire spectral data over thousands of feet depth at high vertical resolution in a fraction of the time that is needed for traditional analytical methods such as XRD or TEM with better accuracy than traditional geologic drill or chip logging that uses visual inspection alone. We have successfully identified layered silicates such as illite, kaolinite, montmorillonite chlorite and prehnite, zeolites, opal, calcite, jarosite and iron oxides 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.

Mg isotope systematics during magmatic processes: Inter-mineral fractionation in mafic to ultramafic Hawaiian xenoliths

NASA Astrophysics Data System (ADS)

Stracke, A.; Tipper, E. T.; Klemme, S.; Bizimis, M.

2018-04-01

Observed differences in Mg isotope ratios between bulk magmatic rocks are small, often on a sub per mill level. Inter-mineral differences in the 26Mg/24Mg ratio (expressed as δ26Mg) in plutonic rocks are on a similar scale, and have mostly been attributed to equilibrium isotope fractionation at magmatic temperatures. Here we report Mg isotope data on minerals in spinel peridotite and garnet pyroxenite xenoliths from the rejuvenated stage of volcanism on Oahu and Kauai, Hawaii. The new data are compared to literature data and to theoretical predictions to investigate the processes responsible for inter-mineral Mg isotope fractionation at magmatic temperatures. Theory predicts up to per mill level differences in δ26Mg between olivine and spinel at magmatic temperatures and a general decrease in Δ26Mgolivine-spinel (=δ26Mgolivine - δ26Mgspinel) with increasing temperature, but also with increasing Cr# in spinel. For peridotites with a simple petrogenetic history by melt depletion, where increasing depletion relates to increasing melting temperatures, Δ26Mgolivine-spinel should thus systematically decrease with increasing Cr# in spinel. However, most natural peridotites, including the Hawaiian spinel peridotites investigated in this study, are overprinted by variable extents of melt-rock reaction, which disturb the systematic primary temperature and compositionally related olivine-spinel Mg isotope systematics. Diffusion, subsolidus re-equilibration, or surface alteration may further affect the observed olivine-spinel Mg isotope fractionation in peridotites, making Δ26Mgolivine-spinel in peridotites a difficult-to-apply geothermometer. The available Mg isotope data on clinopyroxene and garnet suggest that this mineral pair is a more promising geothermometer, but its application is restricted to garnet-bearing igneous (garnet pyroxenites) and metamorphic rocks (eclogites). Although the observed δ26Mg variation is on a sub per mill range in bulk magmatic rocks, the clearly resolvable inter-mineral Mg isotope differences imply that crystallization or preferential melting of isotopically distinct minerals such garnet, spinel, and clinopyroxene should cause Mg isotope fractionation between bulk melt and residue. Calculated Mg isotope variations during partial mantle melting indeed predict differences between melt and residue, but these are analytically resolvable only for melting of mafic lithologies, that is, garnet pyroxenites. Contributions from garnet pyroxenite melts may thus account for some of the isotopically light δ26Mg observed in ocean island basalts and trace lithological mantle heterogeneity. Consequently, applications for high-temperature Mg isotope fractionations are promising and diverse, and recent advances in analytical precision may allow the full petrogenetic potential inherent in the sub per mill variations in δ26Mg in magmatic rocks to be exploited.

P-T Path and Nd-isotopes of Garnet Pyroxenite Xenoliths From Salt Lake Crater, Oahu

NASA Astrophysics Data System (ADS)

Ichitsubo, N.; Takahashi, E.; Clague, D. A.

2001-12-01

Abundant garnet pyroxenite and spinel lherzolite xenoliths are found in Salt Lake Crater (SLC) in Oahu, Hawaii [Jackson and Wright, 1970]. The SLC pyroxenite suite xenoliths (olivine-poor type) have complex exsolution textures that were probably formed during a slow cooling. In this study, we used digital image software to obtain modal data of exsolved phases in the host pyroxene using backscattered electron images (BEIs). The abundances of the exsolved phases were multiplied by the phase compositions determined by electron probe micro-analyzer (EPMA) to reconstruct pyroxene compositions prior to exsolution. In order to evaluate the error in this calculation, we recalculated the reconstructed pyroxene compositions using the different pyroxene pairs. Reconstructed clinopyroxenes in each sample have almost no variations (MgO, CaO +/-1wt %, FeO +/-0.5wt % and the other oxides ~+/-0.1wt %). Reconstructed orthopyroxenes are more variable in MgO, CaO (+/-2wt %) and FeO (+/-1wt %) than reconstructed clinopyroxenes, but the other oxides have only limited variations ( ~+/-0.5wt %). These compositions were used to calculate igneous stage (magmatic) P-T conditions based on the geothermometers and geobarometers of Wells [1977] and Brey and Kohler [1990] Following assumptions are made: (1) the reconstructed pyroxene compositions are the final record in the primary igneous stage, and (2) cores of the largest garnet grains in each sample record the primary igneous stage composition.. The recalculation using the different pairs of reconstructed pyroxenes show the uncertainty to be +/- 30° C and 0.1 GPa. These appear to be small compared to the large intrinsic errors of geothermometer and geobarometers (+/-20° -35° C and +/- 0.3-0.5 GPa). Estimated P-T conditions for garnet pyroxenites are 1.5-2.2 GPa, 1000° -1100° C in the final reequilibration stage and 2.2-2.6 GPa (at maximum), 1150° -1300° C (at minimum) in the igneous stage. The all samples show ca. 200° C cooling and 0.5 GPa decompression. This implies that the garnet pyroxenites cooled ca. 200° C to develop the observed complex exsolution and may have risen from about 70-80 km to 50-65 km depth. Glass pockets and fine minerals (olivine, pyroxene, spinel) occur in the SLC garnet pyroxenite xenoliths. Amphibole and phlogopite, which may have crystallized by metasomatism, are common accessory minerals in them. In order to study the nature of metasomatism as revealed by the glass pockets and fine aggregate of spinel and pyroxene, Nd-isotope study on the SLC xenoliths is under way.

Taking Yellowstone's Temperature: a New Clinopyroxene Geothermometer to Improve Timescales of Pre-eruptive Events

NASA Astrophysics Data System (ADS)

Brugman, K. K.; Till, C. B.

2017-12-01

The goal of our research is to quantify the time period between events in the magma chamber and eruption for the Scaup Lake rhyolite lava, as it erupted after a period of quiescence similar to what Yellowstone is experiencing today. The overarching goal of studies such as this that focus on past eruptions is to provide context and statistics that will ultimately improve volcano monitoring at different types of active volcanoes. The Scaup Lake flow contains zoned minerals (e.g., feldspar, zircon, clinopyroxene) that record multiple magma injection events shortly before they were erupted. Our previous work using nano-scale elemental concentration profiles from zoned clinopyroxene (cpx) as a diffusion dating tool reinforced our hypothesis that different minerals may not record the same series of pre-eruptive events, and that cpx crystal rims record older events in the Scaup Lake flow (on the order of 100s of years prior to eruption [Brugman et al., AGU OSPA talk, 2016]) than do feldspar rims (< 10 months and 10-40 years prior to eruption [Till et al., Geology, 2015]). In light of new temperature data, we have updated our diffusion dating results to better quantify pre-eruption timescales at Yellowstone.

Temperature fluctuation of the Iceland mantle plume through time

NASA Astrophysics Data System (ADS)

Spice, Holly E.; Fitton, J. Godfrey; Kirstein, Linda A.

2016-02-01

The newly developed Al-in-olivine geothermometer was used to find the olivine-Cr-spinel crystallization temperatures of a suite of picrites spanning the spatial and temporal extent of the North Atlantic Igneous Province (NAIP), which is widely considered to be the result of a deep-seated mantle plume. Our data confirm that start-up plumes are associated with a pulse of anomalously hot mantle over a large spatial area before becoming focused into a narrow upwelling. We find that the thermal anomaly on both sides of the province at Baffin Island/West Greenland and the British Isles at ˜61 Ma across an area ˜2000 km in diameter was uniform, with Al-in-olivine temperatures up to ˜300°C above that of average mid-ocean ridge basalt (MORB) primitive magma. Furthermore, by combining our results with geochemical data and existing geophysical and bathymetric observations, we present compelling evidence for long-term (>107 year) fluctuations in the temperature of the Iceland mantle plume. We show that the plume temperature fell from its initial high value during the start-up phase to a minimum at about 35 Ma, and that the mantle temperature beneath Iceland is currently increasing.

Fluid-inclusion technique for determining maximum temperature in calcite and its comparison to the vitrinite reflectance geothermometer

USGS Publications Warehouse

Barker, C.E.; Goldstein, R.H.

1990-01-01

The hypothesis that aqueous fluid inclusions in calcite can be used to establish maximum temperature (Tpeak) is tested. Fluid inclusion Th, mean random vitrinite reflectance (Rm), and present-day Tpeak from 46 diverse geologic systems that have been at Tpeak from 104 to 106 yr have been compiled. Present Tpeak ranged from 65 to 345??C, Th modes and means ranged from 59 to 350??C, and Rm data ranged from 0.4% to 4.6%, spanning the temperature and thermal maturity range associated with burial diagenesis, hydrothermal alteration, and low-grade metamorphism. Plots of Th and Tpeak data for systems thought to be currently at maximum temperature demonstrate close agreement between Th and present Tpeak in sedimentary basins. The relation suggests that Th of aqueous fluid inclusions in calcite may be a useful measure of maximum temperature. This study also compared Th to mean random vitrinite reflectance (Rm). Th correlates well with Rm and results in a curve similar to Rm vs. Tpeak calibrations determined by other workers. Strong correlation between Tpeak and Rm in these systems suggests that maximum temperature is the major control on thermal maturation. -after Authors

Hydrologic and geochemical monitoring in Long Valley Caldera, Mono County, California, 1985

USGS Publications Warehouse

Farrar, C.D.; Sorey, M.L.; Rojstaczer, S.A.; Janik, C.J.; Winnett, T.L.; Clark, M.D.

1987-01-01

Hydrologic and geochemical monitoring, to detect changes caused by magmatic and tectonic processes in the Long Valley caldera has continued through 1985. The monitoring included the collection of the following types of data: chemical and isotopic composition of water and gases from springs, wells, and steam vents; temperatures in wells, springs, and steam vents; flow rates of springs and streams; water levels in wells; and barometric pressure and precipitation at several sites. In addition, reservoir temperatures for the geothermal system were estimated from computations based on chemical geothermometers applied to fluid samples from wells and springs. Estimates of thermal water discharged from springs were made on the basis of boron and chloride fluxes in surface waters for selected sites in the Casa Diablo area and along the Mammoth-Hot Creek drainage. These data are presented in tables and graphs. The Long Valley area was relatively quiescent throughout 1985 in terms of geodetic changes and seismic activity. As a consequence , the hydrologic system varied mainly in response to seasonal influences of temperature, atmospheric pressure, and precipitation. However, spring flows near Casa Diablo were influenced by pumping at the geothermal production well field nearby. (Author 's abstract)

Hydrogeochemistry and reservoir model of Fuzhou geothermal field, China

NASA Astrophysics Data System (ADS)

Huang, H. F.; Goff, Fraser

1986-03-01

Fuzhou geothermal field is a low- to intermediate-temperature geothermal system consisting of meteoric water that circulates deeply along faults. The area of the field is about 9 km 2 but it is elongated in a NNW-trending direction. Fluids in the field are controlled by a series of four NNW extensional faults in Cretaceous granitic basement (Fuzhou fault zone). These faults feed warm waters into overlying permeable Quaternary sediments. The hydrothermal system consists of north and south parts whose chemical compositions are subtly different. In the northern part the system discharges sulfate/chloride waters with relatively low chloride concentrations, but in the south the system discharges chloride waters having relatively high chloride concentrations. Maximum wellhead temperatures are 97°C, which agrees with the chalcedony geothermometer in many cases. Based on the solubility of quartz, the deep-reservoir temperature cannot exceed 123 to 131°C. From heat and mass balance calculations, we conclude that the present total extracted capacity of fluid from the reservoir (20,000 tons/day) could be doubled without noticeable drawdown. We estimate the recoverable heat in the reservoir to be about 1.71 × 10 11 MJ.

Geochemistry and Temperatures Recorded by Zircon During the Final Stages of the Youngest Toba Tuff Magma Chamber, Sumatra, Indonesia

NASA Astrophysics Data System (ADS)

Gaither, T.; Reid, M. R.; Vazquez, J. A.

2009-12-01

The ~74 ka eruption of the Youngest Toba Tuff (YTT) in Sumatra, Indonesia, was one of the largest single volcanic eruptions in geologic history, on par with other voluminous silicic eruptions such as the Huckleberry Ridge Tuff of Yellowstone and the Bishop Tuff of Long Valley, California. We are exploring how zircon and other accessory mineral phases record compositional and thermal changes that occurred in the YTT magma, and the important clues these crystal scale records hold for magma chamber dynamics and processes that lead up to supervolcano eruptions. In this study, we report trace element (REE, U, Th, Ti, and Hf) characteristics, Ti-in-zircon crystallization temperatures, and apparent REE partition coefficients obtained for YTT zircon rims. Twenty-nine zircons from pumices with a compositional range of 70-76 wt% SiO2 were analyzed on the UCLA Cameca ims 1270 ion microprobe. The grains were mounted so that only the outermost ~1.5 microns of the crystals were analyzed. Median Zr/Hf ratios of 34 to 38 characterize zircons from the pumices; the high silica rhyolite grains have lower Zr/Hf. Chondrite-normalized REE patterns are strongly LREE-depleted. Positive Ce anomalies are large (Ce/Ce* ranges up to 88) and Eu/Eu* varies by a factor of four (0.05 to 0.21). Eu/Eu*, Nd/Yb, and Th/U decrease with decreasing Zr/Hf, showing that the variation in zircon rim compositions may be related by co-precipitation of feldspar and allanite along with zircon. Titanium contents also decrease with decreasing Zr/Hf, suggesting that the chemical differences could be related to temperature changes. REE partition coefficients calculated from zircon rim compositions and pumice glass compositions give a good fit to a lattice strain model. They are also quite similar to the partition coefficients of Sano et al. (2002) which have been shown to be successful at reproducing melt compositions in other settings. Temperatures of crystallization calculated using the Ti-in-zircon geothermometer (Watson et al., 1996), assuming a melt aTiO2 of 0.5, yield very low median values (even without a possible pressure correction of -40 to -80°C), ranging from 640-667°C. Virtually all of the zircon rims record temperatures lower than eruption temperatures of 700-780°C estimated for the YTT by Chesner (1998) using FeTi oxide equilibria. It is possible that the low zircon temperatures reflect uncertainties in the Ti-in-zircon geothermometer but they are nonetheless permissive of re-entrainment of zircon from a near-solidus mush close to the time of eruption. The analytically significant chemical variations within the individual zircon populations, especially those of Zr/Hf, Eu/Eu*, and Nd/Yb, suggest that crystals from distinct compositional domains were brought together during a final merging/coalescence of magma that catalyzed the eruption.

Relation of compositions of deep fluids in geothermal activity of Pleistocene-Holocene volcanic fields of Lesser Caucasus

NASA Astrophysics Data System (ADS)

Meliksetian, Khachatur; Lavrushin, Vassily; Shahinyan, Hrach; Aidarkozhina, Altin; Navasardyan, Gevorg; Ermakov, Alexander; Zakaryan, Shushan; Prasolov, Edward; Manucharyan, Davit; Gyulnazaryan, Shushan; Grigoryan, Edmond

2017-04-01

It is widely accepted, that geothermal activity in the conductive heat flow processes, such as volcanism and hydrothermal activity, is manifestation of the thermal mass transfer process in the Earth's crust, where geothermal and geochemical processes are closely connected. Therefore, geochemistry and isotope compositions of thermal mineral waters within and on periphery of volcanic clusters may represent key indicators for better understanding of geothermal activity in geodynamically active zones. Geochemical features of heat and mass transport in hydrothermal systems related to active volcanic and fault systems in continental collision related orogenic elevated plateaus such as Anatolian-Armenian-Iranian highlands are still poorly understood. In this contribution we attempt to fill these gaps in our knowledge of relations of geochemical and geothermal processes in collision zones. We present new data on chemical compositions, trace element geochemistry of thermal waters of Lesser Caucasus, (Armenia) as well as isotope analysis of free gases such as {}3He/{}4He, {}40Ar/{}36Ar, δ{}13?(CO{}2), nitrogen δ{}15N(N{}2) and oxygen and hydrogen isotopes in water phases (δD, δ{}18O). To reveal some specific features of formation of fluid systems related to thermal activity in the areas of collision related active volcanism and active geodynamics a complex geochemical (SiO{}2, K-Na, Na-Li, Li-Mg) and isotope geothermometers (δ{}18O(CaCO{}3) - δ{}18O(H{}2O)) were applied. The distribution of δ{}13?(??{}2) values in free gases of mineral waters of Armenia demonstrates that gases related to Quaternary volcanic fields are characterized by relatively light δ{}13?(CO{}2) values close to mantle derived gases, while on periphery of volcanic systems relatively heavy values of δ{}13?(CO{}2) indicate strong influence of metamorphic and sedimentary derived carbon dioxide. Distribution of nitrogen isotopes δ{}15N(N{}2) demonstrate an inverse correlation with δ{}13?(CO{}2) values and similarly to carbon dioxide indicate presence of metamorphic nitrogen on the periphery and strong influence of atmospheric (and mantle derived) nitrogen within volcanic fields. Results of geochemical and isotope investigations, as well as estimated temperatures of the formation of the mineral compositions of thermal waters demonstrate, that these studied hydrothermal systems originated within thermal anomaly fields associated with young (Pleistocene-Holocene) volcanic fields in Armenia. Basing on geochemical and isotope data, as well as on estimations of temperatures of water formation, calculated using various geothermometers, thermal anomaly fields, related to young volcanic activity and faults, within Armenian and neighboring areas of Lesser Caucasus are outlined. These results are used to reveal potential and promising areas for geothermal energy exploration in Armenia. This research is completed in framework of joint Armenian-Russian research grant funded by State Committee of Science of Armenia (grant #15RF-076) and Russian Foundation for Basic Research (grant#15-55-05069).

New geochemical investigations in Platanares and Azacualpa geothermal sites (Honduras)

NASA Astrophysics Data System (ADS)

Barberi, Franco; Carapezza, Maria Luisa; Cioni, Roberto; Lelli, Matteo; Menichini, Matia; Ranaldi, Massimo; Ricci, Tullio; Tarchini, Luca

2013-05-01

Platanares and Azacualpa geothermal sites of Honduras are located in an inner part of the Caribbean Plate far from the active volcanic front of Central America. Here geology indicates that there are not the conditions for the occurrence of shallow magmatic heat sources for high-enthalpy geothermal resources. Geothermal perspectives are related to the possibility of a deep circulation of meteoric water along faults and the storage of the heated fluid in fractured permeable reservoirs. Geochemical geothermometers indicate a temperature for the deeper part of the geothermal reservoir close to 200 °C for Platanares and of 150-170 °C for Azacualpa. Calcite scaling, with subordinate silica deposition has to be expected in both sites. CO2 soil flux investigations have been carried out in both areas and reveal the presence of positive anomalies likely corresponding to the presence at depth of fractured degassing geothermal reservoirs. Compared with the geothermal areas of Central Italy whose reservoirs are hosted in carbonate rocks, e.g. Latera (Chiodini et al., 2007), the CO2 soil flux measured in Honduras is significantly lower (mean of 17 g/m2day at Platanares and of 163 g/m2day at Azacualpa) probably because of the dominant silicate nature of the deep reservoirs.

Comparative thermometry on pelitic rocks and marbles of the Llano uplift, Texas

DOE Office of Scientific and Technical Information (OSTI.GOV)

Letargo, C.M.R.; Lamb, W.M.

1992-01-01

The Llano Uplift in central Texas is a Grenville-aged metamorphic complex consisting of amphibolite facies assemblages whose development has been attributed to the emplacement of granite plutons between 1.0--1.1 Ga. Temperatures have been obtained from garnet-biotite, garnet-ilmenite, and calcite-dolomite pairs as well as from various silicate equilibria. Application of these geothermometers yield consistent results and are thus indicative of peak conditions attending the amphibolite facies metamorphism. Temperature determined using garnet-biotite and garnet-ilmenite thermometry compare favorably with calcite-dolomite temperatures obtained from marbles in contact with granite plutons in the southeastern part of the uplift. The highest calcite-dolomite temperatures of [approximately]600 Cmore » are obtained from marbles containing an isobarically invariant assemblage consisting of calcite + dolomite + diopside + tremolite + forsterite. At pressures of 2--3 kbar, this isobarically invariant assemblage will be stable at a temperature range of [approximately]600--650 C. Also in close proximity to granites in the southeast uplift is the assemblage muscovite + quartz + k-feldspar + sillimanite [approximately] andalusite which indicate T 650 C and P 2.5 kbar. Assemblages consisting of garnet + sillimanite + quartz + plagioclase (GASP) and garnet + rutile + ilmenite + plagioclase + quartz (GRIPS) are currently being studied to provide additional constraints on pressures of amphibolite facies metamorphism.« less

Near-infrared laboratory spectroscopy of mineral chemistry: A review

NASA Astrophysics Data System (ADS)

Meer, Freek van der

2018-03-01

Spectroscopy is the science concerned with the investigation and measurement of spectra produced when materials interacts with or emits electromagnetic radiation. Commercial infrared spectrometer were designed from the 1950's onward and found their way into the pharmaceutical and chemical industries. In the 1970's and 1980's also natural sciences notably mineralogy and vegetation science started systematically to measure optical properties of leaves and minerals/rocks with spectrometers. In the last decade spectroscopy has made the step from qualitative observations of mineral classes, soil type and vegetation biomass to quantitative estimates of mineral, soil and vegetation chemistry. This resulted in geothermometers used to characterize metamorphic and hydrothermal systems and to the advent of foliar biochemistry. More research is still needed to bridge the gap between laboratory spectroscopy and field spectroscopy. Empirical studies of minerals either as soil or rock constituents (and vegetation parameters) derived from regression analysis of spectra against chemistry is important in understanding the physics of the interaction of electromagnetic radiation and matter which in turn is important in the design of future satellite missions. Physics based models and retrievals are needed to operationalize these relationships and implement them in future earth observation missions as these are more robust and easy to transfer to other areas and data sets.

Hydrogeochemistry Characteristics and Daily Variation of Geothermal Water in the Moxi Fault,Southwest of China

NASA Astrophysics Data System (ADS)

Qi, Jihong; Xu, Mo; An, Chenjiao; Zhang, Yunhui; Zhang, Qiang

2017-04-01

The Xianshuihe Fault with frequent earthquakes activities is the regional deep fault in China. The Moxi Fault is the southern part of the Xianshuihe Fault, where the strong activities of geothermal water could bring abundant information of deep crust. In this article, some typical geothermal springs were collected along the Moxi fault from Kangding to Shimian. Using the the Na-K-Mg equilibrium diagram, it explains the state of water-rock equilibrium, and estimates the reservoir temperature basing appropriate geothermometers. Basing on the relationship between the enthalpy and chlorine concentration of geothermal water, it analyze the mixing progress of thermal water with shallow groundwater. Moreover, the responses of variation of geothermal water to the solid tides are considered to study the hydrothermal activities of this fault. The Guanding in Kangding are considered as the center of the geothermal system, and the hydrothermal activities decrease southward extending. Geothermal water maybe is heated by the deep heat source of the Himalayan granites, while the springs in the south area perform the mixture with thermal water in the sub-reservoir of the Permian crystalline limestone. It improves the research of hydrothermal activities in the Moxi Fault, meanwhile using the variation of geothermal water maybe become a important method to study the environment of deep earth in the future.

Toward a new < 250 °C pyrrhotite-magnetite geothermometer for claystones

NASA Astrophysics Data System (ADS)

Aubourg, Charles; Pozzi, Jean-Pierre

2010-05-01

We investigate the effects of burial and moderate experimental heating on claystones from three regions with different degrees of maturation: immature (burial temperature ˜ 40 °C) of Bure Callovo-Oxfordian claystones in the Basin of Paris (France); early mature (burial temperature ˜ 85 °C) of Opalinus Lower Dogger claystones from the Mont Terri anticline in front of the Jura fold belt (Switzerland); and mature to overmature (burial temperature < 170 °C) of Chartreuse Callovian-Oxfordian claystones from Chartreuse Sub-Alpine chains. To have information about the nature of the magnetic assemblage, we perform low-temperature (10 K-300 K) investigation of an isothermal remanent magnetization. In a first set of laboratory heating experiments, we aim to impart a chemical remanent magnetization (CRM) at 95 °C for several weeks in Bure and Opalinus claystones. Thermal demagnetization of the CRM reveals that magnetite is formed by heating the Opalinus claystones while an assemblage of magnetite and iron sulphide is formed in Bure claystones. Further, we document the appearance of a magnetic transition at ˜ 35 K in Bure claystones after heating. We name this transition the P-transition and we propose that it is related to the formation of fine-grained pyrrhotite (Fe 7S 8). The P-transition is also detected in early mature to mature Opalinus and Chartreuse claystones. We conduct additional experimental heating of natural Opalinus claystones. One set of experiments is referred to as short-term heating (1 h) from 100 °C to 200 °C. It is dedicated to an investigation of the effect of short-lived heating processes in geology. A second set of heating experiments is designed to approach burial conditions using a gold capsule. In burial-like experiments, we heated Opalinus claystones from 150 °C to 250 °C for several weeks under a pressure of 100 MPa. In both experiments, we observe a correlative diminution of the pyrrhotite signature at 35 K with increasing temperature. We interpret this trend as the appearance of magnetite. We derive a parameter PM from the warming curve of a saturated isothermal remanent magnetization acquired at 10 K (ZFC). We report on a consistent evolution of PM with temperature in the range of 40 °C to 250 °C, including natural samples, heated samples at 95 °C, and burial-like heated samples. PM first increases between ˜ 40 °C up to ˜ 85 °C, implying that pyrrhotite gradually dominates the magnetic assemblage at low temperature. For temperatures above 85 °C, PM decreases up to 250 °C, implying that the formation of magnetite gradually overshadows the magnetic input of pyrrhotite. PM values obtained from mature to overmature claystones from the Chartreuse are lower than the PM values obtained from the burial-like heated Opalinus claystones, suggesting that the formation of magnetite is driven by kinetics. The continuous trend of the PM parameter suggests that the magnetic properties of pyrrhotite-magnetite claystones can be used to infer paleo-temperatures and we propose to name this geothermometer MagEval.

The Minimum Potential Temperature of the Hawaiian Mantle is About 1420°C

NASA Astrophysics Data System (ADS)

Gudfinnsson, G. H.; Presnall, D. C.

2002-12-01

Picritic glasses found in turbidite sands near the submarine part of Kilauea's East Rift Zone contain up to 15 wt.% MgO and are the most magnesian Hawaiian volcanic glasses reported to date (Clague et al., 1991, 1995). They have olivine phenocrysts as magnesian as Fo90.7, and when their compositions are plotted together on normative diagrams, they form a distinct olivine fractionation trend. Melt geothermometers indicate that the eruption temperatures of the picrite magmas were as high as about 1320°C. On the assumption that these glasses represent primary melt compositions that coexisted with a lherzolite phase assemblage, the CMASNF geothermometer (Gudfinnsson and Presnall, 2001) yields a maximum temperature of generation of about 1480°C, which corresponds roughly to a pressure of 2.5 GPa. This assumes that the melts were essentially free of H2O and CO2. However, both of these volatile components have the potential to lower significantly the solidus temperatures of mantle peridotite and alter the chemistry of primary melts. The approximately 0.4 wt.% H2O measured in the Hawaiian picrite glasses is probably below the saturation limit for H2O, and can be assumed to be close to the original H2O content of the picrite melts. The measured amount of CO2 in the glasses is low as most CO2 was probably lost by degassing at the time of eruption. The CO2 content of primary magmas at Kilauea has been determined as 0.7 wt.% (Gerlach and Graeber, 1985; Gerlach et al., 2001). Whereas the addition of CO2 tends to shift melts derived from peridotite toward greater alkalinity, the addition of H2O tends to move liquids toward the quartz normative side of the basalt tetrahedron. Results of CO2- and H2O-bearing melting experiments indicate that with the low amounts of H2O and CO2 expected in the primary melts of Kilauea their effect on the position of phase boundaries will be small. From phase relations involving melt in equilibrium with a garnet lherzolite phase assemblage in the system CaO-MgO-Al2O3-SiO2-CO2, we estimate that the solidus temperature of mantle lherzolite is lowered by about 10°C for each 1 wt.% increase in the amount of CO2 in the melt. The effect of H2O is to lower the solidus temperature about 40°C for each 1 wt.% increase in this component. This yields a minimum potential temperature (Tp) for Hawaii of about 1420°C, which is consistent with data indicating at most only a very slight increase of heat flow at Hawaii relative to Pacific crust of the same age (Stein and Stein, 1993). This Tp is 140-160°C higher than petrological estimates of the average Tp of the MORB source (McKenzie and Bickle, 1988; Presnall et al., 2002). Our data do not constrain the upper limit of Tp at Hawaii.

Apacheta, a new geothermal prospect in Northern Chile

DOE Office of Scientific and Technical Information (OSTI.GOV)

Urzua, Luis; Powell, Tom; Cumming, William B.

2002-05-24

The discovery of two high-temperature fumaroles, with gas geochemistry compatible with an economic geothermal system, established Apacheta as one of the most attractive geothermal exploration prospects in northern Chile. These remote fumaroles at 5,150 m elevation were first sampled in 1999 by ENAP and its partners, following up on the reports of a CODELCO water exploration well that flowed small amounts of dry steam at 4,540 m elevation in the valley 4.5 km east of the fumaroles. The prospect is associated with a Plio-Pleistocene volcanic complex located within a NW-trending graben along the axis of the high Andes. The regionalmore » water table is 4,200 masl. There are no hot springs, just the 88 degrees C steam well and the 109 degrees and 118 degrees C fumaroles with gas compositions that indicate reservoir temperatures of greater than or equal to 250 degrees C, using a variety of gas geothermometers. An MT-TDEM survey was completed in 2001-2002 by Geotermica del Norte (SDN), an ENAP-C ODELCO partnership, to explore the Apacheta geothermal concession. The survey results indicated that base of the low resistivity clay cap has a structural apex just west of the fumaroles, a pattern typically associated with shallow permeability within a high temperature geothermal resource. SGN plans to drill at least one exploration well in 2002-03 to characterize a possible economic resource at Apacheta.« less

Chemical Analyses of Ground Water in the Carson Desert near Stillwater, Churchill County, Nevada, 2005

USGS Publications Warehouse

Fosbury, DeEtta; Walker, Mark; Stillings, Lisa L.

2008-01-01

This report presents the chemical analyses of ground-water samples collected in 2005 from domestic wells located in the Stillwater area of the Carson Desert (fig. 1). These data were evaluated for evidence of mixing with nearby geothermal waters (Fosbury, 2007). That study used several methods to identify mixing zones of ground and geothermal waters using trace elements, chemical equilibria, water temperature, geothermometer estimates, and statistical techniques. In some regions, geothermal sources influence the chemical quality of ground water used for drinking water supplies. Typical geothermal contaminants include arsenic, mercury, antimony, selenium, thallium, boron, lithium, and fluoride (Webster and Nordstrom, 2003). The Environmental Protection Agency has established primary drinking water standards for these, with the exception of boron and lithium. Concentrations of some trace metals in geothermal water may exceed drinking water standards by several orders of magnitude. Geothermal influences on water quality are likely to be localized, depending on directions of ground water flow, the relative volumes of geothermal sources and ground water originating from other sources, and depth below the surface from which water is withdrawn. It is important to understand the areal extent of shallow mixing of geothermal water because it may have adverse chemical and aesthetic effects on domestic drinking water. It would be useful to understand the areal extent of these effects.

Oxygen isotope activities and concentrations in aqueous salt solutions at elevated temperatures: Consequences for isotope geochemistry

USGS Publications Warehouse

Truesdell, A.H.

1974-01-01

Studies of the effect of dissolved salts on the oxygen isotope activity ratio of water have been extended to 275??C. Dehydrated salts were added to water of known isotope composition and the solutions were equilibrated with CO2 which was sampled for analysis. For comparison similar studies were made using pure water. Results on water nearly coincide with earlier calculations. Salt effects diminish with increasing temperature only for solutions of MgCl2 and LiCl. Other salt solutions show complex behavior due to the temperature-dependent formation of ion pairs of changing character. Equilibrium fractionations (103 ln ??) between 1 molal solutions and pure water at 25, 100, and 275??C are: NaCl 0.0, -1.5, +1.0; KCl 0.0, -1.0, +2.0; LiCl -1.0, -0.6, -0.5; CaCl2 -0.4, -1.8, +0.8; MgCl2 -1.1, -0.7, -0.3; MgSO4 -1.1, +0.1, -; NaF (0.8 m) 0.0, -1.5, -0.3; and NH4Cl (0.55 m) 0.0, -1.2, -1.3. These effects are significant in the isotope study of hot saline fluids responsible for ore deposition and of fluids found in certain geothermal systems. Minor modification of published isotope geothermometers may be required. ?? 1974.

Spatial and Temporal Changes to Water Chemistry and Heat Flux of the Lake Rotomahana Hydrothermal System

NASA Astrophysics Data System (ADS)

Stucker, V. K.; Tivey, M.; Lupton, J. E.; Walker, S. L.; Fornari, D. J.; de Ronde, C. E. J.

2014-12-01

Lake Rotomahana (North Island, New Zealand) is a crater lake with prominent hydrothermal venting. Water column studies were conducted in 2011 and 2014 to complement magnetic, seismic, bathymetric and heat flux surveys, respectively. Results from the heat flow survey indicate that Lake Rotomahana is getting warmer relative to historic measurements, with individual stations within the lake releasing heat in excess of 60 Watts/m2. Helium sources are found at the lake floor at depths of ~50 meters and ~100m. Helium concentrations below 50 m depth have increased with high statistical significance over the three years between surveys and represent some of the highest concentrations ever measured at 6x107 ccSTP/g with an end-member 3He/4He value of 7.1 Ra. Hydrothermal activity comprises a significant portion of the inputs to Lake Rotomahana, as evidenced by δD and δ18O values, as well as ratios of conservative elements such as boron and chloride. Waters collected from lakeshore hot springs show geographic differences in geothermal source temperature using a Na-K geothermometer, with inferred reservoir temperatures ranging from 200 to 230°C. Lake Rotomahana was in part the focus of the 1886 Tarawera eruption; our results show both pre-eruption hydrothermal sites and newly created post-eruption sites are active and should be monitored for continued changes.

Thermodynamic assessment of the magmatic history of Blue Rock shield volcano, Jackson Co., Oregon: application of a new DNi (olivine-melt) geothermometer and other models

NASA Astrophysics Data System (ADS)

Crabtree, Stephen M.; Huber, Abigail; Beck, Karl

2017-05-01

Blue Rock is a basaltic shield volcano in the southern Oregon Cascades, north of Mt. McLoughlin, showing bulk phenocryst abundances ranging from 5 to 28 vol%, and a variety of groundmass textures. Compositional analyses of olivine and plagioclase phenocrysts and glomerocrysts allowed for the sequential application of a new {D}_{Ni}^{olivine-melt} thermometer, a plagioclase-melt hygrometer, and a viscosity model to define olivine-in conditions for a suite of lavas erupted from this edifice. Calculated olivine-in temperatures were compared to results from the anhydrous MELTS model, and the D (Mg) model of Beattie (1993). Model results were consistent with experimental data for hydrous arc basalts with respect to temperature (1053-1146 °C), dissolved-H2O contents (0.9-2.4 wt% H2O), and viscosity (1.9-2.2 log10 Pa s), confirming the utility of these models in assessing the thermodynamic properties of mafic, hydrous arc lavas over a broad range in crystallinity, requiring only the completion of bulk geochemical and microprobe analyses. These studies also reinforced the significant and predictable role of water, affecting the compositions of crystals grown during magmatic ascent, and allowed the definition of a reasonable multi-stage eruptive sequence consistent with the degassing of magmas on ascent in the formation of this small-scale basaltic edifice.

Chemical, isotopic, and gas compositions of selected thermal springs in Arizona, New Mexico, and Utah

USGS Publications Warehouse

Mariner, R.H.; Presser, T.S.; Evans, William C.

1977-01-01

Twenty-seven thermal springs in Arizona, New Mexico, and Utah were sampled for detailed chemical and isotopic analysis. The springs issue sodium chloride, sodium bicarbonate, or sodium mixed-anion waters of near neutral (6.2) to alkaline (9.2) pH. High concentrations of fluoride, more than 8 milligrams per liter, occur in Arizona in waters from Gillard Hot Springs, Castle Hot Springs, and the unnamed spring of Eagle Creek, and in New Mexico from springs along the Gila River. Deuterium compositions of the thermal waters cover the same range as those expected for meteoric waters in the respective areas. The chemical compositions of the thermal waters indicate that Thermo Hot Springs in Utah and Gillard Hot Springs in Arizona represent hydrothermal systems which are at temperatures higher than 125 deg C. Estimates of subsurface temperature based on the quartz and Na-K-Ca geothermometer differ by up to 60 deg C for Monroe, Joseph, Red Hill, and Crater hot springs in Utah. Similar conflicting estimates of aquifer temperature occur for Verde Hot Springs, the springs near Clifton and Coolidge Dam, in Arizona; and the warm springs near San Ysidro, Radium Hot Springs, and San Francisco Hot Springs, in New Mexico. Such disparities could result from mixing, precipitation of calcium carbonate, or perhaps appreciable concentrations of magnesium. (Woodard-USGS)

Geohydrology, geochemistry, geothermal potency of Rianiate Toba Lake North Sumatera

NASA Astrophysics Data System (ADS)

Nainggolan, Juliper; Sitepu, Cristin; Pardede, Sanggam; Diantoro, Markus

2017-09-01

This research was performed to determine the potency of Rianiate’s geothermal an alternative of energy source and determine the types of geothermal that was begun with the position’s measurement by using GPS (Global Position System), and then the direct observation of chemical and physical properties such as pH, surface’s temperature, color etc. The following steps were taking sample in four different springs indicated by spring 1, spring 2, spring 3, and spring 4. The chemical nature was measured by titrimetry method by using AAS, XRD, and gas Chromathology. The calculating of temperature of subsurface has done by using geothermometer and sequentially followed by geothermal potency’s calculation. The position of four springs are located about N: 02° 31,852’ and E: 098° 44. 021’ where were average height from sea’s level is 958 m. The highest surface’s temperature is 80 °C and the temperature under soil is about 130.5 °C described the average of geothermal. The calculation of content of chloride, sulfate, bicarbonations revealed that the water can be categorized as chloride type. The trilateral diagram Na/1000 - K/100 - √Mg of hot water is in the regime of immature water. From the calculation of Indonesia’s Standardized Geotherm, it was obtained that the estimated reservoir potency of Rianiate geotherm is 2,68 MWe.

Improved EPMA Trace Element Accuracy Using a Matrix Iterated Quantitative Blank Correction

NASA Astrophysics Data System (ADS)

Donovan, J. J.; Wark, D. A.; Jercinovic, M. J.

2007-12-01

At trace element levels below several hundred PPM, accuracy is more often the limiting factor for EPMA quantification rather than precision. Modern EPMA instruments equipped with low noise detectors, counting electronics and large area analyzing crystals can now routinely achieve sensitivities for most elements in the 10 to 100 PPM levels (or even lower). But due to various sample and instrumental artifacts in the x-ray continuum, absolute accuracy is often the limiting factor for ultra trace element quantification. These artifacts have various mechanisms, but are usually attributed to sample artifacts (e.g., sample matrix absorption edges)1, detector artifacts (e.g., Ar or Xe absorption edges) 2 and analyzing crystal artifacts (extended peak tails preventing accurate determination of the true background and ¡§negative peaks¡¨ or ¡§holes¡¨ in the x-ray continuum). The latter being first described3 by Self, et al. and recently documented for the Ti kÑ in quartz geo-thermometer. 4 Ti (ka) Ti (ka) Ti (ka) Ti (ka) Ti (ka) Si () O () Total Average: -.00146 -.00031 -.00180 .00013 .00240 46.7430 53.2563 99.9983 Std Dev: .00069 .00075 .00036 .00190 .00117 .00000 .00168 .00419 The general magnitude of these artifacts can be seen in the above analyses of Ti ka in a synthetic quartz standard. The values for each spectrometer/crystal vary systematically from ¡V18 PPM to + 24 PPM. The exact mechanism for these continuum ¡§holes¡¨ is not known but may be related to secondary lattice diffraction occurring at certain Bragg angles depending on crystal mounting orientation for non-isometric analyzing crystals5. These x-ray continuum artifacts can produce systematic errors at levels up to 100 PPM or more depending on the particular analytical situation. In order to correct for these inaccuracies, a ¡§blank¡¨ correction has been developed that applies a quantitative correction to the measured x-ray intensities during the matrix iteration, by calculating the intensity contribution from the systematic quantitative offset from a known (usually zero level) blank standard. Preliminary results from this new matrix iterated trace element blank correction demonstrate that systematic errors can be reduced to single digit PPM levels for many situations. 1B.W. Robinson, N.G. Ware and D.G.W. Smith, 1998. "Modern Electron-Microprobe Trace-Element Analysis in Mineralogy". In Cabri, L.J. and Vaughan, D.J., Eds. "Modern Approaches to Ore and Environmental Mineralogy", Short Course 27. Mineralogical Association of Canada, Ottawa 153-180 2Remond, G., Myklebust, R. Fialin, M. Nockolds, C. Phillips, M. Roques-Carmes, C. ¡§Decomposition of Wavelength Dispersive X-ray Spectra¡¨, Journal of Research of the National Institute of Standards and Technology (J. Res. Natl. Inst. Stand. Technol., v. 107, 509-529 (2002) 3Self, P.G., Norrish, K., Milnes, A.R., Graham, J. & Robinson, B.W. (1990): Holes in the Background in XRS. X-ray Spectrom. 19 (2), 59-61 4Wark, DA, and Watson, EB, 2006, TitaniQ: A Titanium-in-Quartz geothermometer: Contributions to Mineralogy and Petrology, 152:743-754, doi: 10.1007/s00410-006-0132-308

Geochemistry of water and gas discharges from the Mt. Amiata silicic complex and surrounding areas (central Italy)

NASA Astrophysics Data System (ADS)

Minissale, A.; Magro, G.; Vaselli, O.; Verrucchi, C.; Perticone, I.

1997-12-01

The Mt. Amiata volcano in central Italy is intimately related to the post-orogenic magmatic activity which started in Pliocene times. Major, trace elements, and isotopic composition of thermal and cold spring waters and gas manifestations indicate the occurrence of three main reservoir of the thermal and cold waters in the Mt. Amiata region. The deepest one is located in an extensive carbonate reservoir buried by thick sequences of low-permeability allochthonous and neo-autochthonous formations. Thermal spring waters discharging from this aquifer have a neutral Ca-SO 4 composition due to the presence of anhydrite layers at the base of the carbonate series and, possibly, to absorption of deep-derived H 2S with subsequent oxidation to SO 42- in a system where pH is buffered by the calcite-anhydrite pair ( Marini and Chiodini, 1994). Isotopic signature of these springs and N 2-rich composition of associated gas phases suggest a clear local meteoric origin of the feeding waters, and atmospheric O 2 may be responsible for the oxidation of H 2S. The two shallower aquifers have different chemical features. One is Ca-HCO 3 in composition and located in several sedimentary formations above the Mesozoic carbonates. The other one has a Na-Cl composition and is hosted in marine sediments filling many post-orogenic NW-SE-trending basins. Strontium, Ba, F, and Br contents have been used to group waters associated with each aquifer. Although circulating to some extent in the same carbonate reservoir, the deep geothermal fluids at Latera and Mt. Amiata and thermal springs discharging from their outcropping areas have different composition: Na-Cl and Ca-SO 4 type, respectively. Considering the high permeability of the reservoir rock, the meteoric origin of thermal springs and the two different composition of the thermal waters, self-sealed barriers must be present at the boundaries of the geothermal systems. The complex hydrology of the reservoir rocks greatly affects the reliability of geothermometers in liquid phase, which understimate the real temperatures of the discovered geothermal fields. More reliable temperatures are envisaged by using gas composition-based geothermometers. Bulk composition of the 67 gas samples studied seems to be the result of a continuous mixing between a N 2-rich component of meteoric origin related to the Ca-SO 4 aquifer and a deep CO 2-rich component rising largely along the boundaries of the geothermal systems. Nitrogen-rich gas samples have nearly atmospheric N 2/Ar (=83) and 15N/ 14N ( δ=0‰) ratios whereas CO 2-rich samples show anomalously high δ15N values (up to +6.13 ‰), likely related to N 2 from metamorphic schists lying below the carbonate formations. On the basis of average 13C/ 12C isotopic ratio ( δ13C around 0‰), CO 2 seems to originate mainly from thermometamorphic reactions in the carbonate reservoir and/or in carbonate layers embedded in the underlying metamorphic basement. Distribution of 3He/ 4He isotopic ratios indicates a radiogenic origin of helium in a tectonic environment that, in spite of the presence of many post-orogenic basins and mantle-derived magmatics, can presently be considered in a compressive phase.

Fluid-aided incorporation of Y into almandine-pyrope garnet via coupled dissolution-reprecipitation

NASA Astrophysics Data System (ADS)

Harlov, D. E.

2009-12-01

In nature almandine-pyrope garnet is a well-known host for a variety of trace elements including (Y+HREE), Sr, HFSE, as well as LREE such as Sm and Nd; all of which have important roles with regard to various geological processes (Kohn, 2009, GCA, 73, 170). For example, Y exchange between xenotime and garnet has been empirically calibrated as a geothermometer (Pyle and Spear, 2000, CMP, 138, 51). Sm/Nd and Lu/Hf dating, using garnet, is a well-known geochronometer (Thöni et al., 2008, Chem Geol, 254, 216). In general, REE + HFSE + Sr have been used to chart garnet growth and subsequently the evolution of the host rock (Konrad-Schmolke et al., 2008, EPSL, 272, 488). Incorporation of Y into garnet is probably the most widely studied trace element. These studies range from stress-induced redistribution of Y in garnet (Røhr et al, 2007, Am Mineral, 92, 1276) to Y zoning during garnet growth (Zeh, 2005, J Petrol, 47, 2335). While the incorporation of Y into garnet has generally been thought to occur either via diffusion or during garnet growth, more recent workers have suggested that incorporation of Y could also be fluid-aided. Fluid-aided incorporation of Y into garnet has been tested in the piston-cylinder apparatus (CaF2 assemblies, cylindrical graphite ovens) at 1000 MPa and 900 °C (8 days duration). Here, 10 mg of 50-200 µm size, inclusion-free, gem quality, fragments of the Gore Mountain garnet (Alm40-49, Py37-43, Gr13-16, Sp1) plus 5 mg 2N NaOH and 2 mg Y2O3 were loaded into a 3 mm diameter, 1 cm long, Au capsule that was then arc-welded shut and placed vertically in the CaF2 assembly such that the NiCr thermocouple tip came halfway up along the Au capsule length. Examination of the garnet fragments after the experiment indicates both high Y mobility and the partial alteration of the garnet in the form of a remobilized Y3Al5O12 component enriching those areas of the garnet along the grain rim. The enriched areas take the form of a series of intergrowths with sharp compositional boundaries, which appear to be defined by specific lattice planes as determined by the crystallographic axes of the garnet. These textures are the result of coupled dissolution-reprecipitation (Putnis, 2002, Min Mag, 66, 689), which essentially has resulted in the pseudomorphic partial replacement of a portion of the original garnet by a re-precipitated garnet now enriched in Y. The result from this study suggest that Y may be incorporated into garnet by the aid of fluids, which are both reactive with garnet and in which Y is mobile. In general, this result has strong implications with respect to incorporation of REE (and more specifically HREE) into garnet. It provides a mechanism by which garnet and other Y-bearing minerals, such as xenotime, may equilibrate hence enhancing their use as geothermometers. It also indicates that with respect to both Sm/Nd and Lu/Hf dating, the garnet geochronometer can be reset. More importantly, it implies that diffusion after or inclusion during garnet growth is not the only way by which trace elements may be incorporated into garnet.

Electron Spin Resonance (ESR) studies of returned comet nucleus samples

NASA Technical Reports Server (NTRS)

Tsay, Fun-Dow; Kim, Soon Sam; Liang, Ranty H.

1989-01-01

The most important objective of the Comet Nucleus Sample Returm Mission is to return samples which could reflect formation conditions and evolutionary processes in the early solar nebula. It is expected that the returned samples will consist of fine-grained silicate materials mixed with ices composed of simple molecules such as H2O, NH3, CH4 as well as organics and/or more complex compounds. Because of the exposure to ionizing radiation from cosmic-ray, gamma-ray, and solar wind protons at low temperature, free radicals are expected to be formed and trapped in the solid ice matrices. The kind of trapped radical species together with their concentration and thermal stability can be used as a dosimeter as well as a geothermometer to determine thermal and radiation histories as well as outgassing and other possible alternation effects since the nucleus material was formed. Since free radicals that are known to contain unpaired electrons are all paramagnetic in nature, they can be readily detected and characterized in their native form by the Electron Spin Resonance (ESR) method. In fact, ESR has been shown to be a non-destructive, highly sensitive tool for the detection and characterization of paramagnetic, ferromagnetic, and radiation damage centers in terrestrial and extraterrestrial geological samples. The potential use of ESR as an effective method in the study of returned comet nucleus samples, in particular, in the analysis of fine-grained solid state icy samples is discussed.

The influence of kinetics on the oxygen isotope composition of calcium carbonate

NASA Astrophysics Data System (ADS)

Watkins, James M.; Nielsen, Laura C.; Ryerson, Frederick J.; DePaolo, Donald J.

2013-08-01

Paleotemperature reconstructions rely on knowledge of the equilibrium separation of oxygen isotopes between aqueous solution and calcium carbonate. Although oxygen isotope separation is expected on theoretical grounds, the temperature-dependence remains uncertain because other factors, such as slow exchange of isotopes between dissolved CO2-species and water, can obscure the temperature signal. This is problematic for crystal growth experiments on laboratory timescales and for interpreting the oxygen isotope composition of crystals formed in natural settings. We present results from experiments in which inorganic calcite is precipitated in the presence of 0.25 μM dissolved bovine carbonic anhydrase (CA). The presence of dissolved CA accelerates oxygen isotope equilibration between the dissolved carbon species CO2, H2CO3, HCO3-, CO32- and water, thereby eliminating this source of isotopic disequilibrium during calcite growth. The experimental results allow us to isolate, for the first time, kinetic oxygen isotope effects occurring at the calcite-water interface. We present a framework of ion-by-ion growth of calcite that reconciles our new measurements with measurements of natural cave calcites that are the best candidate for having precipitated under near-equilibrium conditions. Our findings suggest that isotopic equilibrium between calcite and water is unlikely to have been established in laboratory experiments or in many natural settings. The use of CA in carbonate precipitation experiments offers new opportunities to refine oxygen isotope-based geothermometers and to interrogate environmental variables other than temperature that influence calcite growth rates.

Mineral and chemical composition of the Jezersko meteorite—A new chondrite from Slovenia

NASA Astrophysics Data System (ADS)

Miler, Miloš; Ambrožič, Bojan; Mirtič, Breda; Gosar, Mateja; Å turm, Sašo.; Dolenec, Matej; Jeršek, Miha

2014-10-01

The Jezersko meteorite is a newly confirmed stony meteorite found in 1992 in the Karavanke mountains, Slovenia. The meteorite is moderately weathered (W2), indicating short terrestrial residence time. Chondrules in partially recrystallized matrix are clearly discernible but often fragmented and have mean diameter of 0.73 mm. The meteorite consists of homogeneous olivine (Fa19.4) and low-Ca pyroxenes (Fs16.7Wo1.2), of which 34% are monoclinic, and minor plagioclase (Ab83An11Or6) and Ca-pyroxene (Fs6Wo45.8). Troilite, kamacite, zoned taenite, tetrataenite, chromite, and metallic copper comprise about 16.5 vol% of the meteorite. Phosphates are represented by merrillite and minor chlorapatite. Undulatory extinction in some olivine grains and other shock indicators suggests weak shock metamorphism between stages S2 and S3. The bulk chemical composition generally corresponds to the mean H chondrite composition. Low siderophile element contents indicate the oxidized character of the Jezersko parent body. The temperatures recorded by two-pyroxene, olivine-chromite, and olivine-orthopyroxene geothermometers are 854 °C, 737-787 °C, and 750 °C, respectively. Mg concentration profiles across orthopyroxenes and clinopyroxenes indicate relatively fast cooling at temperatures above 700 °C. A low cooling rate of 10 °C Myr-1 was obtained from metallographic data. Considering physical, chemical, and mineralogical properties, meteorite Jezersko was classified as an H4 S2(3) ordinary chondrite.

Temperature constraints on the Ginkgo flow of the Columbia River Basalt Group

NASA Astrophysics Data System (ADS)

Ho, Anita M.; Cashman, Katharine V.

1997-05-01

This study provides the first quantitative estimate of heat loss for a Columbia River Basalt Group flow. A glass composition-based geothermometer was experimentally calibrated for a composition representative of the 500-km-long Ginkgo flow of the Columbia River Basalt Group to measure temperature change during transport. Melting experiments were conducted on a bulk sample at 1 atm between 1200 and 1050 °C. Natural glass was sampled from the margin of a feeder dike near Kahlotus, Washington, and from pillow basalt at distances of 120 km (Vantage, Washington), 350 km (Molalla, Oregon), and 370 km (Portland, Oregon). Ginkgo basalt was also sampled at its distal end at Yaquina Head, Oregon (500 km). Comparison of the glass MgO content, K2O in plagioclase, and measured crystallinities in the experimental charges and natural samples tightly constrains the minimum flow temperature to 1085 ± 5 °C. Glass and plagioclase compositions indicate an upper temperature of 1095 ± 5 °C; thus the maximum temperature decrease along the flow axis of the Ginkgo is 20 °C, suggesting cooling rates of 0.02 0.04 °C/km. These cooling rates, substantially lower than rates observed in active and historic flows, are inconsistent with turbulent flow models. Calculated melt temperatures and viscosities of 240 750 Pa · s allow emplacement either as a fast laminar flow under an insulating crust or as a slower, inflated flow.

Qrtzgeotherm: An ActiveX component for the quartz solubility geothermometer

NASA Astrophysics Data System (ADS)

Verma, Mahendra P.

2008-12-01

An ActiveX component, QrtzGeotherm, to calculate temperature and vapor fraction in a geothermal reservoir using quartz solubility geothermometry was written in Visual Basic 6.0. Four quartz solubility equations along the liquid-vapor saturation curve: (i) a quadratic equation of 1/ T and pressure, (ii) a linear equation relating log SiO 2 to the inverse of absolute temperature ( T), (iii) a polynomial of T including logarithmic terms and (iv) temperature as a polynomial of SiO 2 including logarithmic terms are programmed. The QrtzGeotherm has input parameters: (i) HRes—the reservoir enthalpy (kJ/kg), (ii) SiO2TD—silica concentration in total discharge (ppm), (iii) GeoEq—number of quartz solubility equation and (iv) TempGuess—a guess value of the reservoir temperature (°C). The reservoir enthalpy Hres is assumed to be the same as the total discharge enthalpy HR. The output parameters are (i) TempRes—reservoir temperature (°C) and (ii) VapRes—reservoir vapor fraction. The first step is to calculate the total discharge concentration of silica SiO2TD from the concentration of silica SiO2Col of separated water, sampled after N-separations of vapor and water. To use QrtzGeotherm in MS-Excel, three functions SiO2TD, GeoResTemp and GeoResVap for an N-stage separation of geothermal reservoir fluid are written in Visual Basic for Application (VBA). Similarly, a demonstration program, QrtzGeothrm, is written in Visual Basic 6.0.

Multireaction equilibrium geothermometry: A sensitivity analysis using data from the Lower Geyser Basin, Yellowstone National Park, USA

USGS Publications Warehouse

King, Jonathan M.; Hurwitz, Shaul; Lowenstern, Jacob B.; Nordstrom, D. Kirk; McCleskey, R. Blaine

2016-01-01

A multireaction chemical equilibria geothermometry (MEG) model applicable to high-temperature geothermal systems has been developed over the past three decades. Given sufficient data, this model provides more constraint on calculated reservoir temperatures than classical chemical geothermometers that are based on either the concentration of silica (SiO2), or the ratios of cation concentrations. A set of 23 chemical analyses from Ojo Caliente Spring and 22 analyses from other thermal features in the Lower Geyser Basin of Yellowstone National Park are used to examine the sensitivity of calculated reservoir temperatures using the GeoT MEG code (Spycher et al. 2013, 2014) to quantify the effects of solute concentrations, degassing, and mineral assemblages on calculated reservoir temperatures. Results of our analysis demonstrate that the MEG model can resolve reservoir temperatures within approximately ±15°C, and that natural variation in fluid compositions represents a greater source of variance in calculated reservoir temperatures than variations caused by analytical uncertainty (assuming ~5% for major elements). The analysis also suggests that MEG calculations are particularly sensitive to variations in silica concentration, the concentrations of the redox species Fe(II) and H2S, and that the parameters defining steam separation and CO2 degassing from the liquid may be adequately determined by numerical optimization. Results from this study can provide guidance for future applications of MEG models, and thus provide more reliable information on geothermal energy resources during exploration.

Hydrogeochemical characteristics and genesis of the high-temperature geothermal system in the Tashkorgan basin of the Pamir syntax, western China

NASA Astrophysics Data System (ADS)

Li, Yiman; Pang, Zhonghe; Yang, Fengtian; Yuan, Lijuan; Tang, Pinghui

2017-11-01

High-temperature geothermal systems in China, such as those found in Tenchong and Tibet, are common. A similar system without obvious manifestations found in the Tashkorgan basin in the western Xinjiang Autonomous Region, however, was not expected. The results from borehole measurements and predictions with geothermometers, such as quartz, Na-K and Na-K-Mg, indicate that the reservoir temperature is approximately 250-260 °C. Geothermal water is high in Total Dissolved Solids (>2.5 g/L) and SiO2 content (>273 mg/L), and the water type is Cl·SO4-Na, likely resulting from water-rock interactions in the granodiorite reservoirs. Based on isotope analysis, it appears to be recharged by local precipitation and river water. Evidence from the relationships between major ions and the Cl and molar Na/Cl ratio suggests mixing between deep geothermal water and shallow cold groundwater during the upwelling process. Mixing ratios calculated by the relationship between Cl and SiO2 show that the proportion from cold end-members are 96-99% and 40-90% for riparian zone springs and geothermal water from boreholes, respectively. Active regional tectonic and Neo-tectonic movements in the Pamir syntax as well as radioactive elements in the granodiorite reservoir of the Himalayan stage provide basis for the high heat flow background (150-350 mW/m2). NNW trending fault systems intersecting with overlying NE faults provide circulation conduits with high permeability for geothermal water.

Paleogeothermal record of the Emeishan mantle plume: evidences from borehole Ro data in the Sichuan basin, SW China

NASA Astrophysics Data System (ADS)

Hu, S.

2013-12-01

The Emeishan basalt province located in the southwest of China is widely accepted to be a result of the eruption of a mantle plume at the time of middle-late Permian. If it was a mantle plume, the ambient sedimentary rocks must be heated up during the development of the mantle plume and this thermal effect must be recorded by some geothermometers in the country rocks. The vitrinite reflectance (Ro) data as a maximum paleotemperature recorder from boreholes in Sichuan basin was employed to expose the thermal regime related to the proposed Emeishan mantle plume. The Ro profiles from boreholes which drilled close to the Emeishan basalts shows a ';dog-leg' (break) style at the unconformity between the middle and the upper Permian, and the Ro profiles in the lower subsection (pre-middle Permian) shows a significantly higher slopes (gradients) than those in the upper subsection. In contrast, those Ro profiles from boreholes far away from the center of the basalt province have no break at the uncomformity. Based on the chemical kinetic model of Ro, the paleo-temperature gradients for the upper and the lower subsections in different boreholes, as well as the erosion at the unconformity between the middle and the upper Permian, were reconstructed to reveal the variations of the temperature gradients and erosion thickness with geological time and space. Both the thermal regime and the erosion thickness together with their spatial variation (structure) provide strong geothermal evidence for the existence of the Emeishan mantle plume in the middle-late Permian.

A geochemical model of the Platanares geothermal system, Honduras

USGS Publications Warehouse

Janik, C.J.; Truesdell, A.H.; Goff, F.; Shevenell, L.; Stallard, M.L.; Trujillo, P.E.; Counce, D.

1991-01-01

Results of exploration drilling combined with results of geologic, geophysical, and hydrogeochemical investigations have been used to construct a geochemical model of the Platanares geothermal system, Honduras. Three coreholes were drilled, two of which produced fluids from fractured Miocene andesite and altered Cretaceous to Eocene conglomerate at 450 to 680 m depth. Large volume artesian flows of 160-165??C, predominantly bicarbonate water are chemically similar to, but slightly less saline than widespread boiling hot-spring waters. The chemistry of the produced fluid is dominated by equilibrium reactions in sedimentary rocks at greater depths and higher temperatures than those measured in the wells. Chemical, isotope, and gas geothermometers indicate a deep fluid temperature of 200-245??C and reflect a relatively short residence time in the fractures feeding the wells. Chloride-enthalpy relations as well as isotopic and chemical compositions of well discharges, thermal springs, and local cold waters support a conceptual model of ascending high-temperature (minimum 225??C) parent fluid that has cooled conductively to form the 160-165??C shallow (to 680 m) fluid encountered by the wells. The hot-spring waters are formed by boiling and steam loss from more or less conductively cooled parent fluid. The more dilute boiling spring waters (Cl = ???32 mg/kg) have cooled from > 225??C to about 160??C by conduction and from 160??C to 98??C by boiling. The most concentrated boiling spring waters (Cl = 37 mg/kg) have cooled from > 225??C to about 200??C by conduction and from 200??C to 98??C by boiling. Intermediate concentrations reflect mixed cooling paths. ?? 1991.

3-Dimensional Geologic Modeling Applied to the Structural Characterization of Geothermal Systems: Astor Pass, Nevada, USA

DOE Office of Scientific and Technical Information (OSTI.GOV)

Siler, Drew L; Faulds, James E; Mayhew, Brett

2013-04-16

Geothermal systems in the Great Basin, USA, are controlled by a variety of fault intersection and fault interaction areas. Understanding the specific geometry of the structures most conducive to broad-scale geothermal circulation is crucial to both the mitigation of the costs of geothermal exploration (especially drilling) and to the identification of geothermal systems that have no surface expression (blind systems). 3-dimensional geologic modeling is a tool that can elucidate the specific stratigraphic intervals and structural geometries that host geothermal reservoirs. Astor Pass, NV USA lies just beyond the northern extent of the dextral Pyramid Lake fault zone near the boundarymore » between two distinct structural domains, the Walker Lane and the Basin and Range, and exhibits characteristics of each setting. Both northwest-striking, left-stepping dextral faults of the Walker Lane and kinematically linked northerly striking normal faults associated with the Basin and Range are present. Previous studies at Astor Pass identified a blind geothermal system controlled by the intersection of west-northwest and north-northwest striking dextral-normal faults. Wells drilled into the southwestern quadrant of the fault intersection yielded 94°C fluids, with geothermometers suggesting a maximum reservoir temperature of 130°C. A 3-dimensional model was constructed based on detailed geologic maps and cross-sections, 2-dimensional seismic data, and petrologic analysis of the cuttings from three wells in order to further constrain the structural setting. The model reveals the specific geometry of the fault interaction area at a level of detail beyond what geologic maps and cross-sections can provide.« less

Results of investigation at the Miravalles geothermal field, Costa Rica. Resultados de las investigaciones en el campo geotermico de Miravalles, Costa Rica; Parte 2, Muestreo de fluidos pozo abajo

DOE Office of Scientific and Technical Information (OSTI.GOV)

Grigsby, C.O.; Goff, F.; Trujillo, P.E. Jr.

Samples of the geothermal fluids in the Miravalles, Costa Rica, geothermal system were collected from production wellbores using downhole fluid samplers, from flowing wellheads using miniseparators, and from hot springs that discharge in the area. The reservoir fluid at Miravalles is a neutral-chloride-type water, but fumaroles and acid-sulfate springs are present within the main thermal area, and there are bicarbonate-rich hot springs that are clearly related to the neutral-chloride reservoir fluids. Dissolved gases are primarily a mixture of CO{sub 2} with air, but samples collected in the fumarolic areas also contain H{sub 2}S. Water-stable isotope analyses suggest local meteoric recharge,more » and the reservoir fluid shows oxygen isotopic shifts of about 2.5% due to high-temperature oxygen exchange between water and rock. Chemical geothermometer temperatures are consistent with the measured downhole temperature of 220{degrees} to 255{degrees}C. This pattern of neutral-chloride reservoir fluids with acid-sulfate springs near the source region and bicarbonate-rich chloride hot springs at the periphery of the system suggests a lateral outflow type of hydrothermal system. In addition to the geochemical evidence, temperature profiles from several of the wells show temperature reversals that are characteristic of lateral outflow plumes. We find no evidence for the underlying, higher temperature (300{degrees}C) system, which has been suggested by other investigators. 24 refs., 14 figs., 6 tabs.« less

Temporal variation in chemical composition of phenocrysts and magmatic temperature at Daisen volcano, southwest Japan

NASA Astrophysics Data System (ADS)

Tsukui, Masashi

1985-12-01

Daisen volcano, located in the San'in district, southwest Japan, started its activity in the middle Pleistocene and continued until at least ca. 20,000 yr B.P. The volcano is composed entirely of dacitic pyroclastic materials, lava domes and subordinate thick lava flows. Its activity is divided into two groups, Older (1.0-0.4 Ma) and Younger (0.4 Ma to ca. 17.000 yr B.P.). Chemical compositions of phenocrysts in the members of the Upper Tephra Group (the last 150,000 years) in the Younger Group were examined in detail by electron microprobe analysis. The compositions of phenocryst minerals change systematically and cyclically with the order of eruptions. Phenocrysts with less differentiated compositions were found in the products of eruptions 60,000 and 20,000 years ago. The variation patterns of inferred magma temperature (estimated by the Fe-Ti oxide geothermometer) with time are well correlated with those of the chemical compositions of phenocrysts. Orthopyroxene phenocrysts generally show both reversed and normal zoning in single rock specimens and the compositional range of rims is much smaller than that of the core, indicating that the process of re-equilibration of two compositionally distinct orthopyroxenes took place. These facts could be explained by injection of less differentiated, higher-temperature magmas from a deeper level into the shallower more differentiated magma reservoir. A relatively active (frequent and/or voluminous) injection episode seems to have taken place twice during the last 150,000 years; 60,000 and 20,000 years ago.

Vitrinite reflectance and Raman spectra of carbonaceous material as indicators of frictional heating on faults: Constraints from friction experiments

NASA Astrophysics Data System (ADS)

Furuichi, Hiroyuki; Ujiie, Kohtaro; Kouketsu, Yui; Saito, Tsubasa; Tsutsumi, Akito; Wallis, Simon

2015-08-01

Vitrinite reflectance (Ro) and Raman spectra of carbonaceous material (RSCM) are both widely used as indicators of the maximum attained temperatures in sedimentary and metamorphic rocks. However, the potential of these methods to estimate temperature increases associated with fault slip has not been closely studied. To examine this issue, friction experiments were conducted on a mixture of powdered clay-rich fault material and carbonaceous material (CM) at slip rates of 0.15 mm/s and 1.3 m/s in nitrogen (N2) gas with or without distilled water. After the experiments, we measured Ro and RSCM and compared to those in starting material. The results indicate that when fault material suffers rapid heating at >500 °C in ∼9 s at 1.3 m/s, Ro and the intensity ratio of D1 and D2 Raman bands of CM (ID2/ID1) markedly increase. Comminution with very small temperature rise in ∼32 min at 0.15 mm/s is responsible for very limited changes in Ro and ID2/ID1. Our results demonstrate that Ro and RSCM could be useful for the detection of frictional heating on faults when the power density is ≥0.52 MW/m2. However, the conventionally used Ro and RSCM geothermometers are inadequate for the estimation of peak temperature during seismic fault slip. The reaction kinetics incorporating the effects of rapid heating at high slip rates and studies of the original microtexture and composition of CM are required to establish a reliable thermometer for frictional heating on faults.

BACA Project: geothermal demonstration power plant. Final report

DOE Office of Scientific and Technical Information (OSTI.GOV)

Not Available

1982-12-01

The various activities that have been conducted by Union in the Redondo Creek area while attempting to develop the resource for a 50 MW power plant are described. The results of the geologic work, drilling activities and reservoir studies are summarized. In addition, sections discussing the historical costs for Union's involvement with the project, production engineering (for anticipated surface equipment), and environmental work are included. Nineteen geothermal wells have been drilled in the Redondo Creek area of the Valles Caldera: a prominent geologic feature of the Jemez mountains consisting of Pliocene and Pleistocene age volcanics. The Redondo Creek area ismore » within a complex longitudinal graben on the northwest flank of the resurgent structural dome of Redondo Peak and Redondo Border. The major graben faults, with associated fracturing, are geologically plausible candidates for permeable and productive zones in the reservoir. The distribution of such permeable zones is too erratic and the locations too imprecisely known to offer an attractive drilling target. Log analysis indicates there is a preferred mean fracture strike of N31W in the upper portion of Redondo Creek wells. This is approximately perpendicular to the major structure in the area, the northeast-striking Redondo Creek graben. The geothermal fluid found in the Redondo Creek reservoir is relatively benign with low brine concentrations and moderate H/sub 2/S concentrations. Geothermometer calculations indicate that the reservoir temperature generally lies between 500/sup 0/F and 600/sup 0/F, with near wellbore flashing occurring during the majority of the wells' production.« less

Pétrologie d'un complexe gabbroïque différencié dans le sillon du Boussouma (Burkina-Faso-Craton Ouest Africain)

NASA Astrophysics Data System (ADS)

Wenmega, U.; Tempier, P.

Boussouma birimian gabbroic complex is a genetic association of early ultramafic cumulates (retromorphic cortlandite and clinopyroxenite) overlain by tholeiitic rocks formed by massive or layered metagabbros and basic metavolcanites and pillow lavas. Intrusive later in birimian pyroclastic and schistosed volcanodetrictic rocks, this non deformed gabbroic complex, shows multiphased metamorphism surimposition, varying from amphibolite facies of low temperature to epizonal facies. The cristallogenetic sequence composed in cortlandite cumulates by spinel-olivine-orthopyroxene-clinopyroxene-brown hornblende ± plagioclase, joined to temperature (1300° C to 1100° C at 10 kb) furnished by geothermometer couple (orthopyroxene-augite), give a mantellic character to magma and indicate some high thermodynamic condition for cristallization of early cortlandite cumulate. The differenciation is accomplished by satured water and silica magma, in a magmatic chamber toward a slow sedimentation of early ferromagnesia cumulus (olivine-orthopyroxene) in cortlandite. The consequence of this fractionation, is the enrichment of clinopyroxene, brown hornblende, plagioclase, particularly in clinopyroxenites and gabbros facies. Comparatively to classic ophiolitic associations this complex is distinguishable from them by his intrusif character, later in birimian rocks series, by the absence of mantellic sequence (tectonites of harzburgite, lherzolite), by the absence of structural charriage characters in this complex, one criterion generally associated with subduction history of oceanic crust. About geotectonic context of this complex, his cristallogenetic, thermodynamic, geochemical characteristics could evoke one section of fringing basin crust, corresponding to ocean-continent transition zones, or one section of rift valley crust with immature evolution.

Implications of ground water chemistry and flow patterns for earthquake studies.

PubMed

Guangcai, Wang; Zuochen, Zhang; Min, Wang; Cravotta, Charles A; Chenglong, Liu

2005-01-01

Ground water can facilitate earthquake development and respond physically and chemically to tectonism. Thus, an understanding of ground water circulation in seismically active regions is important for earthquake prediction. To investigate the roles of ground water in the development and prediction of earthquakes, geological and hydrogeological monitoring was conducted in a seismogenic area in the Yanhuai Basin, China. This study used isotopic and hydrogeochemical methods to characterize ground water samples from six hot springs and two cold springs. The hydrochemical data and associated geological and geophysical data were used to identify possible relations between ground water circulation and seismically active structural features. The data for delta18O, deltaD, tritium, and 14C indicate ground water from hot springs is of meteoric origin with subsurface residence times of 50 to 30,320 years. The reservoir temperature and circulation depths of the hot ground water are 57 degrees C to 160 degrees C and 1600 to 5000 m, respectively, as estimated by quartz and chalcedony geothermometers and the geothermal gradient. Various possible origins of noble gases dissolved in the ground water also were evaluated, indicating mantle and deep crust sources consistent with tectonically active segments. A hard intercalated stratum, where small to moderate earthquakes frequently originate, is present between a deep (10 to 20 km), high-electrical conductivity layer and the zone of active ground water circulation. The ground water anomalies are closely related to the structural peculiarity of each monitoring point. These results could have implications for ground water and seismic studies in other seismogenic areas.

Implications of ground water chemistry and flow patterns for earthquake studies

USGS Publications Warehouse

Guangcai, W.; Zuochen, Z.; Min, W.; Cravotta, C.A.; Chenglong, L.

2005-01-01

Ground water can facilitate earthquake development and respond physically and chemically to tectonism. Thus, an understanding of ground water circulation in seismically active regions is important for earthquake prediction. To investigate the roles of ground water in the development and prediction of earthquakes, geological and hydrogeological monitoring was conducted in a seismogenic area in the Yanhuai Basin, China. This study used isotopic and hydrogeochemical methods to characterize ground water samples from six hot springs and two cold springs. The hydrochemical data and associated geological and geophysical data were used to identify possible relations between ground water circulation and seismically active structural features. The data for ??18O, ??D, tritium, and 14C indicate ground water from hot springs is of meteoric origin with subsurface residence times of 50 to 30,320 years. The reservoir temperature and circulation depths of the hot ground water are 57??C to 160??C and 1600 to 5000 m, respectively, as estimated by quartz and chalcedony geothermometers and the geothermal gradient. Various possible origins of noble gases dissolved in the ground water also were evaluated, indicating mantle and deep crust sources consistent with tectonically active segments. A hard intercalated stratum, where small to moderate earthquakes frequently originate, is present between a deep (10 to 20 km), high-electrical conductivity layer and the zone of active ground water circulation. The ground water anomalies are closely related to the structural peculiarity of each monitoring point. These results could have implications for ground water and seismic studies in other seismogenic areas. Copyright ?? 2005 National Ground Water Association.

Experimental study of Fe-Mg- and Ca-distribution between coexisting ortho- and clinopyroxenes at P=294 MPa, T=750 and 800° C

NASA Astrophysics Data System (ADS)

Fonarev, V. I.; Graphchikov, A. A.

1982-07-01

The Fe-Mg-Ca-distribution was investigated in synthesis experiments and with the mineral assemblage orthopyroxene+clinopyroxene+quartz. The phase compositions were identified by X-ray diffraction and, where possible, by electron microprobe. The attainment of equilibrium in the run products was signalled by the compositions from control runs (different solutions) becoming closely similar, by recycling runs, by the attainment of equilibrium from different directions (depending on the composition of starting phases), and by special kinetic experiments. The study produced the following results: (1) the Ca content of the clinopyroxenes decreases with increasing Fe (mol%) from 48.4 at X {Cpx/Fe}=5 to 39.8 at X {Cpx/Fe}=45 (800° C); from 47.6 at X {Cpx/Fe}= 10 to 41.7 at X {Cpx/Fe}=45 (750° C); increasing temperature expands the stability field of the less calcic clinopyroxenes. (2) The Ca content of orthopyroxenes increases slightly with Fe content from 1.8 at X {Opx/Fe}=20.5 to 3.2 at X {Opx/Fe}=75; the temperature effect on the Ca content under the T, P conditions of the experiment was not large. (3) Fe and Mg distribution between the coexisting ortho-and clinopyroxenes is largely temperature-dependent, particularly in the compositional range X {Opx/Fe}=15 75 mol%; as T increases, Fe redistributes from the rhombic to monoclinic mineral. Preliminary estimates of rock formation temperatures using the obtained data show that most of the known two-pyroxene geothermometers overstate the actual values by 50 150° C.

New evidence on the hydrothermal system in Long Valley caldera, California, from wells, fluid sampling, electrical geophysics, and age determinations of hot-spring deposits

USGS Publications Warehouse

Sorey, M.L.; Suemnicht, G.A.; Sturchio, N.C.; Nordquist, G.A.

1991-01-01

Data collected since 1985 from test drilling, fluid sampling, and geologic and geophysical investigations provide a clearer definition of the hydrothermal system in Long Valley caldera than was previously available. This information confirms the existence of high-temperature (> 200??C) reservoirs within the volcanic fill in parts of the west moat. These reservoirs contain fluids which are chemically similar to thermal fluids encountered in the central and eastern parts of the caldera. The roots of the present-day hydrothermal system (the source reservoir, principal zones of upflow, and the magmatic heat source) most likely occur within metamorphic basement rocks beneath the western part of the caldera. Geothermometer-temperature estimates for the source reservoir range from 214 to 248??C. Zones of upflow of hot water could exist beneath the plateau of moat rhyolite located west of the resurgent dome or beneath Mammoth Mountain. Lateral flow of thermal water away from such upflow zones through reservoirs in the Bishop Tuff and early rhyolite accounts for temperature reversals encountered in most existing wells. Dating of hot-spring deposits from active and inactive thermal areas confirms previous interpretations of the evolution of hydrothermal activity that suggest two periods of extensive hot-spring discharge, one peaking about 300 ka and another extending from about 40 ka to the present. The onset of hydrothermal activity around 40 ka coincides with the initiation of rhyolitic volcanism along the Mono-Inyo Craters volcanic chain that extends beneath the caldera's west moat. ?? 1991.

On the origin of the Neoproterozoic Peresopolis graphite deposit, Paraguay Belt, Brazil

NASA Astrophysics Data System (ADS)

Manoel, Talitta Nunes; Dexheimer Leite, Jayme Alfredo

2018-07-01

The Peresopolis graphite deposit is located northeast of Brasilândia Town in Mato Grosso State (Brazil). It consists of an 1800 m long, 200 m wide low-crystallinity graphite-bearing tabular layer that trends ENE and dips 65°ESE. The deposit is hosted in carbonaceous phyllites, which along with basal metadiamictites and upper metarenites make up the upper unit (Coxipó Formation) of the Cuiabá Group in the late Cryogenian to Cambrian Paraguay Belt (ca. 650-500Ma). The carbonaceous phyllites show a mineral assemblage consisting mostly of graphite-quartz-muscovite-albite and pyrite and dolomite to a lesser extent; alteration minerals include tosudite and kaolinite. XRD analysis confirmed the gangue material and defined the graphite as low-order crystallinity. Carbon isotope data for graphite ore returned a light and very restricted range of δ13Corg between -29 and -28‰ suggesting organic matter as the source of carbon. One hundred and sixty measurements of Raman graphite spectrum returned a well-fit between full width at half maximum parameter (FWHM) which allowed its use as a geothermometer. Resulting temperatures are in the range between 285 and 300 °C ± 30 °C, indicating low-to very-low metamorphic conditions for transformation of organic matter into amorphous graphite. The deposition of the organic matter should have taken place in an outer slope of a glaciomarine system and its transformation into the ore occurred because of deformation and low-grade metamorphism related to the development of the Neoproterozoic Brasiliano/Pan-African Orogeny (850-500Ma).

Possible TCRM acquisition of the Kilauea 1960 lava, Hawaii: failure of the Thellier paleointensity determination inferred from equilibrium temperature of the Fe-Ti oxide

NASA Astrophysics Data System (ADS)

Yamamoto, Y.

2006-08-01

Natural rock samples may not always be the ideal material for the Thellier-type method as they occasionally result in high paleointensities. The Kilauea 1960 lava, Hawaii, is one such example. Several previous studies have suggested that one of the possible causes for this undesirable behavior is an acquisition of thermochemical remanent magnetization (TCRM) during lava formation. In order to examine this possibility quantitatively, equilibrium temperatures of titanomagnetite grains, which are associated with samples previously subjected to Thellier experiments, are estimated by a Fe-Ti oxide geothermometer. The results show that two specimens from the rock magnetic group giving relatively ideal Thellier paleointensities have clustered equilibrium temperatures of about 800-900 and 700-800°C @. In contrast, two swarmed temperatures around 300 and 700°C were observed for the specimen from a group yielding high paleointensities. Although these are semi-quantitative estimates, when the time scales of Fe-Ti interdiffusion and lava cooling are taken into consideration, the last specimen could have acquired the TCRM during its formation. For such specimens, simple calculation predicts that TCRM/TRM (thermoremanent magnetization) ratios could be 1.19-1.72 for the blocking temperature range of 400-480°C, assuming a grain-growth model. The extent of this overestimation (20-70 %) is comparable to the magnitude of the observations. It is therefore suggested that attention be paid to titanomagnetite grains with well-developed ilmenite lamellae, as these could be potential sources of overestimations of Thellier paleointensities of up to a few tenths of percentage points.

Peak Metamorphic Temperature Profile across Eastern Belt Franciscan, Northern California Coast Ranges

NASA Astrophysics Data System (ADS)

Schmidt, W. L.; Platt, J. P.

2017-12-01

Previous work done on metamorphic temperatures across the lawsonite-albite to blueschist facies rocks of the Eastern Belt of the Franciscan accretionary complex has relied on a combination of many methods, and suggests that temperature broadly increases from west to east. The Taliaferro Metamorphic Complex is an exception to this pattern and shows higher pressures, and possibly higher temperatures, than its surroundings. The exact location and nature of the faults separating accreted packets in the Eastern Belt is somewhat controversial. A recently calibrated low-temperature laser Raman geothermometer for use on carbonaceous material provides a uniform method of estimating peak metamorphic temperature across the eastern Franciscan and is here used to identify the position of major tectonic boundaries. Temperatures were obtained from exposures in Thomes Creek, Cottonwood Creek, Grindstone Creek, and the middle fork of the Eel River. Peak T in the South Fork Mountain Schist, the highest grade and easternmost unit in the Franciscan, is 310-375°C, whereas in immediately underlying lawsonite-albite facies rocks below the Log Springs thrust, peak T is 270 - 300°C. The Taliaferro Metamorphic Complex reached a peak temperature of 336°C, whereas the surrounding lawsonite-albite facies rocks yield peak temperatures as low as 232°C. Preliminary temperature profiles clearly allow the major faults bounding the Taliaferro Metamorphic Complex and the South Fork Mountain Schist to be located. Extension of the temperature profile has the potential to reveal further detail within these units and the lower grade rocks surrounding them.

Mineral chemistry indicates the petrogenesis of rhyolite from the southwestern Okinawa Trough

NASA Astrophysics Data System (ADS)

Chen, Zuxing; Zeng, Zhigang; Wang, Xiaoyuan; Zhang, Yuxiang; Yin, Xuebo; Chen, Shuai; Ma, Yao; Li, Xiaohui; Qi, Hanyan

2017-12-01

To reveal the petrogenesis of rhyolite from the southwestern Okinawa Trough, the mineral chemistry of plagioclase, orthopyroxene, amphibole, quartz and Fe-Ti oxide phenocrysts were analyzed using an electron microprobe, and in suit Sr and Ba contents of plagioclase analysed by LA-ICPMS were chosen for fingerprinting plagioclases of different provenances. Results indicate an overall homogeneous composition for each of the mineral phases except for plagioclase phenocrysts which have a wide range of composition (An=39 88). Plagioclase crystals characterized by An contents of >70 are not in equilibrium with their whole-rock compositions, and coarse-sieved plagioclase phenocryst interiors record high An contents (>70) and Sr/Ba ratios (>7), which are similar to the those of plagioclase crystals in basalt. Therefore, these crystals must have been introduced to the rhyolitic magma from a more mafic source. Equilibrium temperatures estimated using orthopyroxene-liquid, iron-titanium oxide, titanium-in-quartz and amphibole geothermometers show consistent values ranging from 792 to 869°C. The equilibrium pressure calculated using amphibole compositions is close to 121 MPa which corresponds to an approximate depth of 4 km. The fO2 conditions estimated from Fe-Ti oxides and amphiboles plot slightly above the NNO buffer, which indicates that the rock formed under more oxidized conditions. Our results suggests that petrogenesis of the rhyolite due to basaltic magma ascend with the high An and Sr/Ba plaigoclases from deep magma chamber into the shallow chamber where the fractional crystallization and crustal assimilation happened. It also indicates that a two-layer magma chamber structure may occur under the southwestern Okinawa Trough.

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

NASA Astrophysics Data System (ADS)

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.

Geochemical and isotopic evidence on the recharge and circulation of geothermal water in the Tangshan Geothermal System near Nanjing, China: implications for sustainable development

NASA Astrophysics Data System (ADS)

Lu, Lianghua; Pang, Zhonghe; Kong, Yanlong; Guo, Qi; Wang, Yingchun; Xu, Chenghua; Gu, Wen; Zhou, Lingling; Yu, Dandan

2018-01-01

Geothermal resources are practical and competitive clean-energy alternatives to fossil fuels, and study on the recharge sources of geothermal water supports its sustainable exploitation. In order to provide evidence on the recharge source of water and circulation dynamics of the Tangshan Geothermal System (TGS) near Nanjing (China), a comprehensive investigation was carried out using multiple chemical and isotopic tracers (δ2H, δ18O, δ34S, 87Sr/86Sr, δ13C, 14C and 3H). The results confirm that a local (rather than regional) recharge source feeds the system from the exposed Cambrian and Ordovician carbonate rocks area on the upper part of Tangshan Mountain. The reservoir temperature up to 87 °C, obtained using empirical as well as theoretical chemical geothermometers, requires a groundwater circulation depth of around 2.5 km. The temperature of the geothermal water is lowered during upwelling as a consequence of mixing with shallow cold water up to a 63% dilution. The corrected 14C age shows that the geothermal water travels at a very slow pace (millennial scale) and has a low circulation rate, allowing sufficient time for the water to become heated in the system. This study has provided key information on the genesis of TGS and the results are instructive to the effective management of the geothermal resources. Further confirmation and even prediction associated with the sustainability of the system could be achieved through continuous monitoring and modeling of the responses of the karstic geothermal reservoir to hot-water mining.

Sea water - basalt interactions and genesis of the coastal thermal waters of Maharashtra, India

DOE Office of Scientific and Technical Information (OSTI.GOV)

Muthuraman, K.

1986-01-01

The thermal waters close to the western coastal belt of India (in Maharashtra State) generally discharge Na-Ca-Cl and Ca-Na-Cl types of waters through the basic lava flows of late Cretaceous-early Tertiary age. Experimental work to study the reactions between the dilute sea water and basalt conducted in static autoclaves at selected elevated temperatures, indicates the possibility of producing chloride waters with relatively high calcium, similar to these thermal waters. In view of the increase in Ca in the resultant solutions during sea water-basalt reactions at elevated temperatures, the base temperatures computed by Na-K-Ca geothermometry would be far lower than themore » actual temperatures of the system. At lower temperatures (around 100/sup 0/C) absorption by K by basalt is possible and, hence, alkali geothermometry also may not be reliable for such systems. Anhydrite saturation temperature seems to be a reliable geothermometer for such coastal thermal water systems involving a sea water component. The results of the computer processing of the chemistry of some of these thermal waters using ''WATEQ'' are discussed. Two of these waters are oversaturated with diopside, tremolite, calcite and aragonite, indicating a rather low temperature of origin. In two other cases, interaction with ultramafic rocks is indicated, as these waters are oversaturated with diopside, tremolite, talc, chrysotile, sepiolite and its precipitate. There is no clear evidence to show that the thermal waters of the west coast of India emerge directly from either marine evaporites or oil field waters. It is proposed that the majority of these thermal waters should have originated through interaction of an admixture of sea water and meteoric water with the local basalt flows at some elevated temperatures.« less

Trace and minor elements in sphalerite from metamorphosed sulphide deposits

NASA Astrophysics Data System (ADS)

Lockington, Julian A.; Cook, Nigel J.; Ciobanu, Cristiana L.

2014-12-01

Sphalerite is a common sulphide and is the dominant ore mineral in Zn-Pb sulphide deposits. Precise determination of minor and trace element concentrations in sulphides, including sphalerite, by Laser-Ablation Inductively-Coupled-Plasma Mass-Spectrometry (LA-ICP-MS) is a potentially valuable petrogenetic tool. In this study, LA-ICP-MS is used to analyse 19 sphalerite samples from metamorphosed, sphalerite-bearing volcanic-associated and sedimentary exhalative massive sulphide deposits in Norway and Australia. The distributions of Mn, Fe, Co, Cu, Ga, Se, Ag, Cd, In, Sn, Sb, Hg, Tl, Pb and Bi are addressed with emphasis on how concentrations of these elements vary with metamorphic grade of the deposit and the extent of sulphide recrystallization. Results show that the concentrations of a group of trace elements which are believed to be present in sphalerite as micro- to nano-scale inclusions (Pb, Bi, and to some degree Cu and Ag) diminish with increasing metamorphic grade. This is interpreted as due to release of these elements during sphalerite recrystallization and subsequent remobilization to form discrete minerals elsewhere. The concentrations of lattice-bound elements (Mn, Fe, Cd, In and Hg) show no correlation with metamorphic grade. Primary metal sources, physico-chemical conditions during initial deposition, and element partitioning between sphalerite and co-existing sulphides are dominant in defining the concentrations of these elements and they appear to be readily re-incorporated into recrystallized sphalerite, offering potential insights into ore genesis. Given that sphalerite accommodates a variety of trace elements that can be precisely determined by contemporary microanalytical techniques, the mineral has considerable potential as a geothermometer, providing that element partitioning between sphalerite and coexisting minerals (galena, chalcopyrite etc.) can be quantified in samples for which the crystallization temperature can be independently constrained.

Geothermal GIS coverage of the Great Basin, USA: Defining regional controls and favorable exploration terrains

USGS Publications Warehouse

Coolbaugh, M.F.; Sawatzky, D.L.; Oppliger, G.L.; Minor, T.B.; Raines, G.L.; Shevenell, L.; Blewitt, G.; Louie, J.N.

2003-01-01

A geographic information system (GIS) of geothermal resources, built last year for the state of Nevada, is being expanded to cover the Great Basin, USA. Data from that GIS is being made available to industry, other researchers, and the public via a web site at the Great Basin Center for Geothermal Energy, Reno, Nevada. That web site features a search engine, supports ArcExplorer?? for on-line map construction, and provides downloadable data layers in several formats. Though data collection continues, preliminary analysis has begun. Contour maps of geothermal temperatures, constructed using geothermometer temperatures calculated from a Great Basin geochemical database compiled by the Geo-Heat Center, reveal distinctive trends and patterns. As expected, magmatic-type and extensional-type geothermal systems have profoundly different associations, with magmatic-type systems following major tectonic boundaries, and extensional-type systems associating with regionally high heat flow, thin crust, active faulting, and high extensional strain rates. As described by earlier researchers, including Rowen and Wetlaufer (1981) and Koenig and McNitt (1983), high-temperature (> 100??C) geothermal systems appear to follow regional northeast trends, most conspicuously including the Humboldt structural zone in Nevada, the "Black Rock-Alvord Desert" trend in Oregon and Nevada, and the "Newcastle-Roosevelt" trend in Utah and Nevada. Weights-of-evidence analyses confirm a preference of high-temperature geothermal systems for young northeast-trending faults, but the distribution of geothermal systems correlates even better with high rates of crustal extension, as measured from global positioning system (GPS) stations in Nevada. A predictive map of geothermal potential based only on areas of high extensional strain rates and high heat flux does an excellent job of regionally predicting the location of most known geothermal systems in Nevada, and may prove useful in identifying blind systems.

Thermal maturation of carbonaceous material from Mbuji-Mayi Supergroup (Kasai, Democratic Republic of Congo).

NASA Astrophysics Data System (ADS)

Baludikay, Blaise K.; Storme, Jean-Yves; Baudet, Daniel; François, Camille; Javaux, Emmanuelle

2016-04-01

The Mbuji-Mayi Supergroup is a sedimentary sequence in DRC unaffected by regional metamorphism. It consists of two distinct successions: a lower, ~500 m thick siliciclastic sequence of the BI Group and an upper, ~1000 m thick carbonate sequence with stromatolitic build-ups and black shales of the BII Group directly overlain by basaltic lavas [1]. Radiometric data suggest a Latest Meso- to Early Neoproterozoic age [2, 3, 4, and 5]. A well preserved and diversified microfossil assemblage is reported including 54 taxa belonging to 32 genera. The potential Late Mesoproterozoic-Tonian index fossil Trachyhystrichosphaera aimika, is reported for the first time in central Africa, and co-occurs with other eukaryotes and prokaryotes [6]. Thermal maturation calculated on macerate residues, using geothermometer for low-grade metamorphism [7] reveals thermal palaeoenvironments of organic matter, ranging from 180 to 279° C (average = 249 ± 37 °C). The range of thermal maturity is similar, in both microfossils and amorphous organic matter. Raman reflectance (RmcRo %), which is also an index indicative of maturity [8], ranges from 1.05 to 2.55 % (average = 2.01 ± 0.42 %). So, organic matter from Mbuji-Mayi is likely into a maturation stage corresponding to oil window. References: [1] Raucq (1957) Ann. MRAC, série 8, Sc. géol. 18, 427. [2] Cahen & Snelling (1966) Publ. C., Amsterdam. [3] Cahen et al. (1984) Clarendon Press, Oxford. [4] Delpomdor et al. (2013) Pal.3 389, 4-34. [5] François et al. (in preparation). [6] Baludikay et al. (in review) Prec. Res. [7] Kouketsu et al. (2014) Island Arc 23, 33-50. [8] Liu et al. (2013) Geochemistry, Chi. Sc. Bul. 58 (11), 1285-1298.

Generation and evolution of hydrothermal fluids at Yellowstone: Insights from the Heart Lake Geyser Basin

NASA Astrophysics Data System (ADS)

Lowenstern, J. B.; Bergfeld, D.; Evans, W. C.; Hurwitz, S.

2012-01-01

We sampled fumaroles and hot springs from the Heart Lake Geyser Basin (HLGB), measured water and gas discharge, and estimated heat and mass flux from this geothermal area in 2009. The combined data set reveals that diverse fluids share an origin by mixing of deep solute-rich parent water with dilute heated meteoric water, accompanied by subsequent boiling. A variety of chemical and isotopic geothermometers are consistent with a parent water that equilibrates with rocks at 205°C ± 10°C and then undergoes 21% ± 2% adiabatic boiling. Measured diffuse CO2 flux and fumarole compositions are consistent with an initial dissolved CO2 concentration of 21 ± 7 mmol upon arrival at the caldera boundary and prior to southeast flow, boiling, and discharge along the Witch Creek drainage. The calculated advective flow from the basin is 78 ± 16 L s-1of parent thermal water, corresponding to 68 ± 14 MW, or ˜1% of the estimated thermal flux from Yellowstone. Helium and carbon isotopes reveal minor addition of locally derived crustal, biogenic, and meteoric gases as this fluid boils and degasses, reducing the He isotope ratio (Rc/Ra) from 2.91 to 1.09. The HLGB is one of the few thermal areas at Yellowstone that approaches a closed system, where a series of progressively boiled waters can be sampled along with related steam and noncondensable gas. At other Yellowstone locations, steam and gas are found without associated neutral Cl waters (e.g., Hot Spring Basin) or Cl-rich waters emerge without significant associated steam and gas (Upper Geyser Basin).

Insights into Andean slope hydrology: reservoir characteristics of the thermal Pica spring system, Pampa del Tamarugal, northern Chile

NASA Astrophysics Data System (ADS)

Scheihing, Konstantin W.; Moya, Claudio E.; Tröger, Uwe

2017-09-01

The thermal Pica springs, at ˜1,400 m above sea level (asl) in the Pampa del Tamarugal (Chile), represent a low-saline spring system at the eastern margin of the hyper-arid Atacama Desert, where groundwater resources are scarce. This study investigates the hydrogeological and geothermal characteristics of their feed reservoir, fostered by the interpretation of a 20-km east-west-heading reflection-seismic line in the transition zone from the Andean Precordillera to the Pampa del Tamarugal. Additional hydrochemical, isotope and hydrologic time-series data support the integrated analysis. One of the main factors that enabled the development of the spring-related vertical fracture system at Pica, is a disruption zone in the Mesozoic Basement caused by intrusive formations. This destabilized the younger Oligocene units under the given tectonic stress conditions; thus, the respective groundwater reservoir is made up of fractured Oligocene units of low to moderate permeability. Groundwater recharge takes place in the Precordillera at ˜3,800 m asl. From there groundwater flow covers a height difference of ˜3,000 m with a maximum circulation depth of ˜800-950 m, where the waters obtain their geothermal imprint. The maximal expected reservoir temperature, as confirmed by geothermometers, is ˜55 °C. Corrected mean residence times of spring water and groundwater plot at 1,200-4,300 years BP and yield average interstitial velocities of 6.5-22 m/year. At the same time, the hydraulic head signal, as induced by recharge events in the Precordillera, is transmitted within 20-24 months over a distance of ˜32 km towards the Andean foothills at Pica and Puquio Nunez.

Geothermal pilot study final report: creating an international geothermal energy community

DOE Office of Scientific and Technical Information (OSTI.GOV)

Bresee, J.C.; Yen, W.W.S.; Metzler, J.E.

The Geothermal Pilot Study under the auspices of the Committee on the Challenges of Modern Society (CCMS) was established in 1973 to apply an action-oriented approach to international geothermal research and development, taking advantage of the established channels of governmental communication provided by the North Atlantic Treaty Organization (NATO). The Pilot Study was composed of five substudies. They included: computer-based information systems; direct application of geothermal energy; reservoir assessment; small geothermal power plants; and hot dry rock concepts. The most significant overall result of the CCMS Geothermal Pilot Study, which is now complete, is the establishment of an identifiable communitymore » of geothermal experts in a dozen or more countries active in development programs. Specific accomplishments include the creation of an international computer file of technical information on geothermal wells and fields, the development of studies and reports on direct applications, geothermal fluid injection and small power plants, and the operation of the visiting scientist program. In the United States, the computer file has aready proven useful in the development of reservoir models and of chemical geothermometers. The state-of-the-art report on direct uses of geothermal energy is proving to be a valuable resource document for laypersons and experts in an area of increasing interest to many countries. Geothermal fluid injection studies in El Salvador, New Zealand, and the United States have been assisted by the Reservoir Assessment Substudy and have led to long-range reservoir engineering studies in Mexico. At least seven small geothermal power plants are in use or have been planned for construction around the world since the Small Power Plant Substudy was instituted--at least partial credit for this increased application can be assigned to the CCMS Geothermal Pilot Study. (JGB)« less

Chemical and isotopic equilibrium between CO 2 and CH 4 in fumarolic gas discharges: Generation of CH 4 in arc magmatic-hydrothermal systems

NASA Astrophysics Data System (ADS)

Fiebig, Jens; Chiodini, Giovanni; Caliro, Stefano; Rizzo, Andrea; Spangenberg, Jorge; Hunziker, Johannes C.

2004-05-01

The chemical and isotopic composition of fumarolic gases emitted from Nisyros Volcano, Greece, and of a single gas sample from Vesuvio, Italy, was investigated in order to determine the origin of methane (CH 4) within two subduction-related magmatic-hydrothermal environments. Apparent temperatures derived from carbon isotope partitioning between CH 4 and CO 2 of around 340°C for Nisyros and 470°C for Vesuvio correlate well with aquifer temperatures as measured directly and/or inferred from compositional data using the H 2O-H 2-CO 2-CO-CH 4 geothermometer. Thermodynamic modeling reveals chemical equilibrium between CH 4, CO 2 and H 2O implying that carbon isotope partitioning between CO 2 and CH 4 in both systems is controlled by aquifer temperature. N 2/ 3He and CH 4/ 3He ratios of Nisyros fumarolic gases are unusually low for subduction zone gases and correspond to those of midoceanic ridge environments. Accordingly, CH 4 may have been primarily generated through the reduction of CO 2 by H 2 in the absence of any organic matter following a Fischer-Tropsch-type reaction. However, primary occurrence of minor amounts of thermogenic CH 4 and subsequent re-equilibration with co-existing CO 2 cannot be ruled out entirely. CO 2/ 3He ratios and δ 13C CO 2 values imply that the evolved CO 2 either derives from a metasomatized mantle or is a mixture between two components, one outgassing from an unaltered mantle and the other released by thermal breakdown of marine carbonates. The latter may contain traces of organic matter possibly decomposing to CH 4 during thermometamorphism.

Hydrothermal heat discharge in the Cascade Range, northwestern United States

USGS Publications Warehouse

Ingebritsen, S.E.; Mariner, R.H.

2010-01-01

Hydrothermal heat discharge in the Cascade Range includes the heat discharged by thermal springs, by "slightly thermal" springs that are only a few degrees warmer than ambient temperature, and by fumaroles. Thermal-spring heat discharge is calculated on the basis of chloride-flux measurements and geothermometer temperatures and totals ~ 240 MW in the U.S. part of the Cascade Range, excluding the transient post-1980 discharge at Mount St. Helens (~80 MW as of 2004-5). Heat discharge from "slightly thermal" springs is based on the degree of geothermal warming (after correction for gravitational potential energy effects) and totals ~. 660. MW. Fumarolic heat discharge is calculated by a variety of indirect and direct methods and totals ~160 MW, excluding the transient mid-1970s discharge at Mount Baker (~80 MW) and transient post-1980 discharge at Mount St. Helens (>. 230. MW as of 2005). Other than the pronounced transients at Mount St. Helens and Mount Baker, hydrothermal heat discharge in the Cascade Range appears to be fairly steady over a ~25-year period of measurement. Of the total of ~. 1050. MW of "steady" hydrothermal heat discharge identified in the U.S. part of the Cascade Range, less than 50. MW occurs north of latitude 45??15' N (~0.1 MW per km arc length from 45??15' to 49??N). Much greater rates of hydrothermal heat discharge south of 45??15'N (~1.7 MW per km arc length from 40?? to 45??15'N) may reflect the influence of Basin and Range-style extensional tectonics (faulting) that impinges on the Cascades as far north as Mount Jefferson but is not evident farther north. ?? 2010.

Detection of Frictional Heating on Faults Using Raman Spectra of Carbonaceous Material

NASA Astrophysics Data System (ADS)

Ito, K.; Ujiie, K.; Kagi, H.

2017-12-01

Raman spectra of carbonaceous material (RSCM) have been used as geothermometer in sedimentary and metamorphic rocks. However, it remains poorly understood whether RSCM are useful for detecting past frictional heating on faults. To detect increased heating during seismic slip, we examine the thrust fault in the Jurassic accretionary complex, central Japan. The thrust fault zone includes 10 cm-thick cataclasite and a few mm-thick dark layer. The cataclasite is characterized by fragments of black and gray chert in the black carbonaceous mudstone matrix. The dark layer is marked by intensely cracked gray chert fragments in the dark matrix of carbonaceous mudstone composition, which bounds the fractured gray chert above from the cataclasite below. The RSCM are analyzed for carbonaceous material in the cataclasite, dark layer, and host rock <10 mm from cataclasite and dark layer boundaries. The result indicates that there is no increased carbonization in the cataclasite. In contrast, the dark layer and part of host rocks <2 mm from the dark layer boundaries show prominent increase in carbonization. The absent of increased carbonization in the cataclasite could be attributed to insufficient frictional heating associated with distributed shear and/or faulting at low slip rates. The dark layer exhibits the appearance of fault and injection veins, and the dark layer boundaries are irregularly embayed or intensely cracked; these features have been characteristically observed in pseudotachylytes. Therefore, the increased carbonization in the dark layer is likely resulted from increased heating during earthquake faulting. The intensely cracked fragments in the dark layer and cracked wall rocks may reflect thermal fracturing in chert, which is caused by heat conduction from the molten zone. We suggest that RSCM are useful for the detection of increased heating on faults, particularly when the temperature is high enough for frictional melting and thermal fracturing.

Exploration drilling and reservoir model of the Platanares geothermal system, Honduras, Central America

USGS Publications Warehouse

Goff, F.; Goff, S.J.; Kelkar, S.; Shevenell, L.; Truesdell, A.H.; Musgrave, J.; Rufenacht, H.; Flores, W.

1991-01-01

Results of drilling, logging, and testing of three exploration core holes, combined with results of geologic and hydrogeochemical investigations, have been used to present a reservoir model of the Platanares geothermal system, Honduras. Geothermal fluids circulate at depths ??? 1.5 km in a region of active tectonism devoid of Quaternary volcanism. Large, artesian water entries of 160 to 165??C geothermal fluid in two core holes at 625 to 644 m and 460 to 635 m depth have maximum flow rates of roughly 355 and 560 l/min, respectively, which are equivalent to power outputs of about 3.1 and 5.1 MW(thermal). Dilute, alkali-chloride reservoir fluids (TDS ??? 1200 mg/kg) are produced from fractured Miocene andesite and Cretaceous to Eocene redbeds that are hydrothermally altered. Fracture permeabillity in producing horizons is locally greater than 1500 and bulk porosity is ??? 6%. A simple, fracture-dominated, volume-impedance model assuming turbulent flow indicates that the calculated reservoir storage capacity of each flowing hole is approximately 9.7 ?? 106 l/(kg cm-2), Tritium data indicate a mean residence time of 450 yr for water in the reservoir. Multiplying the natural fluid discharge rate by the mean residence time gives an estimated water volume of the Platanares system of ??? 0.78 km3. Downward continuation of a 139??C/km "conductive" gradient at a depth of 400 m in a third core hole implies that the depth to a 225??C source reservoir (predicted from chemical geothermometers) is at least 1.5 km. Uranium-thorium disequilibrium ages on calcite veins at the surface and in the core holes indicate that the present Platanares hydrothermal system has been active for the last 0.25 m.y. ?? 1991.

Update on Production Chemistry of the Roosevelt Hot Springs Reservoir

DOE Office of Scientific and Technical Information (OSTI.GOV)

Simmons, Stuart; Kirby, Stefan; Allis, Rick

Analyses of production fluids from the Roosevelt Hot Springs reservoir were acquired from well sampling campaigns in 2015 and 2016. The resulting data have been recalculated to reservoir conditions by correcting for effects of steam loss, and the values are compared to legacy data from earlier reports to quantify changes with time in response to fluid production. The reservoir composition is similar to that at the start of reservoir exploitation, having near neutral pH, total dissolved solids of 7000-10,000 mg/kg, and ionic ratios of Cl/HCO3 ~50-100, Cl/SO4 ~50-100, and Na/K ~4-5. Cation, gas and silica geothermometers indicate a range ofmore » equilibration temperatures between 240 and 300 °C, but quartz-silica values are most closely consistent with measured reservoir temperatures and well enthalpies. The largest change in fluid composition is observed in well 54-3. The fluid has evolved from being fed by a single phase liquid to a twophase mixture of steam and liquid due to pressure draw down. The fluid also shows a 25% increase in reservoir chloride and a ~20° C decrement of cooling related to mixing with injected brine. The other production wells also show increase in chloride and decrease in temperature, but these changes diminish in magnitude with distance from injection well 14-2. Stable isotope compositions indicate that the reservoir water is largely meteoric in origin, having been modified by hydrothermal waterrock interaction. The water has also become progressively enriched in isotopic values in response to steam loss and mixing of injectate. N2-Ar-He and helium isotope ratios indicate a deep magmatic source region that probably supplies the heat for the hydrothermal system, consistent with recent Quaternary volcanism in the Mineral Mountains.« less

Chemical and stable-radiogenic isotope compositions of Polatlı-Haymana thermal waters (Ankara, Turkey)

NASA Astrophysics Data System (ADS)

Akilli, Hafize; Mutlu, Halim

2016-04-01

Complex tectono-magmatic evolution of the Anatolian land resulted in development of numerous geothermal areas through Turkey. The Ankara region in central Anatolia is surrounded by several basins which are filled with upper Cretaceous-Tertiary sediments. Overlying Miocene volcanics and step faulting along the margins of these basins played a significant role in formation of a number of low-enthalpy thermal waters. In this study, chemical and isotopic compositions of Polatlı and Haymana geothermal waters in the Ankara region are investigated. The Polatlı-Haymana waters with a temperature range of 24 to 43 °C are represented by Ca-(Na)-HCO3 composition implying derivation from carbonate type reservoir rocks. Oxygen-hydrogen isotope values of the waters are conformable with the Global Meteoric Water Line and point to a meteoric origin. The carbon isotopic composition in dissolved inorganic carbon (DIC) of the studied waters is between -21.8 and -1.34 permil (vs. VPDB). Marine carbonates and organic rocks are the main sources of carbon. There is a high correlation between oxygen (3.7 to 15.0 permil; VSMOW) and sulfur (-9.2 to 19.5 permil; VCDT) isotope compositions of sulfate in waters. The mixing of sulfate from dissolution of marine carbonates and terrestrial evaporite units is the chief process behind the observed sulfate isotope systematics of the samples. 87Sr/86Sr ratios of waters varying from 0.705883 to 0.707827 are consistent with those of reservoir rocks. The temperatures calculated by SO4-H2O isotope geothermometry are between 81 and 138 °C nearly doubling the estimates from chemical geothermometers.

Zircon-scale insights into the history of a Supervolcano, Bishop Tuff, Long Valley, California, with implications for the Ti-in-zircon geothermometer

USGS Publications Warehouse

Reid, M.R.; Vazquez, J.A.; Schmitt, A.K.

2011-01-01

Zircon has the outstanding capacity to record chronological, thermal, and chemical information, including the storage history of zoned silicic magma reservoirs like the one responsible for the Bishop Tuff of eastern California, USA. Our novel ion microprobe approach reveals that Bishop zircon rims with diverse chemical characteristics surround intermediate domains with broadly similar compositions. The highest Y, REE, U, and Th concentrations tend to accompany the largest excesses in Y + REE3+:P beyond what can be explained by xenotime substitution in zircon. Apparent Ti-in-zircon temperatures of <720??C for zircon rims are distinctly lower than most of the range in eruption temperatures, as estimated from FeTi-oxide equilibria and zircon solubility at quench. While permissive of crystallization of zircon at near-solidus conditions, the low Ti-in-zircon temperatures are probably better explained by sources of inaccuracy in the temperature estimates. After apparently nucleating from different melts, zircons from across the Bishop Tuff compositional spectrum may have evolved to broadly similar chemical and thermal conditions and therefore it is possible that there was no significant thermal gradient in the magma reservoir at some stage in its evolution. There is also no compelling evidence for punctuated heat ?? chemical influxes during the intermediate stages of zircon growth. Judging by the zircon record, the main volume of the erupted magma evolved normally by secular cooling but the latest erupted portion is characterized by a reversal in chemistry that appears to indicate perfusion of the magma reservoir by-or zircon entrainment in-a less evolved melt from the one in which the zircons had previously resided. ?? 2010 Springer-Verlag.

Generation and evolution of hydrothermal fluids at Yellowstone: Insights from the Heart Lake Geyser Basin

USGS Publications Warehouse

Lowenstern, J. B.; Bergfeld, D.; Evans, William C.; Hurwitz, S.

2012-01-01

We sampled fumaroles and hot springs from the Heart Lake Geyser Basin (HLGB), measured water and gas discharge, and estimated heat and mass flux from this geothermal area in 2009. The combined data set reveals that diverse fluids share an origin by mixing of deep solute-rich parent water with dilute heated meteoric water, accompanied by subsequent boiling. A variety of chemical and isotopic geothermometers are consistent with a parent water that equilibrates with rocks at 205°C ± 10°C and then undergoes 21% ± 2% adiabatic boiling. Measured diffuse CO2 flux and fumarole compositions are consistent with an initial dissolved CO2 concentration of 21 ± 7 mmol upon arrival at the caldera boundary and prior to southeast flow, boiling, and discharge along the Witch Creek drainage. The calculated advective flow from the basin is 78 ± 16 L s−1 of parent thermal water, corresponding to 68 ± 14 MW, or –1% of the estimated thermal flux from Yellowstone. Helium and carbon isotopes reveal minor addition of locally derived crustal, biogenic, and meteoric gases as this fluid boils and degasses, reducing the He isotope ratio (Rc/Ra) from 2.91 to 1.09. The HLGB is one of the few thermal areas at Yellowstone that approaches a closed system, where a series of progressively boiled waters can be sampled along with related steam and noncondensable gas. At other Yellowstone locations, steam and gas are found without associated neutral Cl waters (e.g., Hot Spring Basin) or Cl-rich waters emerge without significant associated steam and gas (Upper Geyser Basin).

Application of remote sensing analysis and MT method for identification geothermal prospect zone in Mt. Endut

NASA Astrophysics Data System (ADS)

Akbar, A. M.; Permadi, A. N.; Wildan, D.; Sobirin, R.; Supriyanto

2017-07-01

Mount Endut is located at Banten Province, 40 km southward Rangkasbitung City, with geographic UTM position between 9261000-9274000 N and 639000-652000 E. Preliminary survey at Mt. Endut was geological and geochemical survey in 2006, resistivity survey and MT survey in 2007 with 27 measurement point. All survey conducted by Pusat Sumber Daya Geologi (PSDG). According to result of premilinary survey, Mt. Endut is dominated by quartenary volcanic rock produced by Mt. Endut, which breakthrough tertiary sediment layer. NE to SW normal fault produced surface manifestation, namely Cikawah (CKW) hot spring and Handeleum (HDL) hot spring. According to SiO2 and NaK geothermometer, subsurface temperature of Mt Endut is ranging from 162 to 180 °C. Apparent resistivity maps show that thermal manifestation areas coincide with pronounced high anomaly due to resistive intrusion bodies contrast to conductive sedimentary basements. In order to delineate permeability zone, fracture fault density (FFD) analysis from remote sensing image is carry out. FFD analysis from lansdat 7 image shows the area on westward flank of Mt. Endut have high fracture fault density (162-276 m/km2), higher than it's surrounding area and can be assume that area is weak zone and have high permeability. That's structure density anomaly coincide with low resistivity from Magnetotelluric data. Resistivity structure from Magnetotelluric data shows western flank have low permeability layer (14-27 Ohmm) with average thickness 250 m. Below this layer there is layer with higher resistivity (37-100 Ohmm) with ±1000 m depth and interpreted as shallow reservoir. Massive resistif intrusive bodies act controlled the surface manifestation, and act as boundary and bounded the geothermal system in western part of Mt. Endut.

Geochemical features of the geothermal fluids from the Mapamyum non-volcanic geothermal system (Western Tibet, China)

NASA Astrophysics Data System (ADS)

Wang, Peng; Chen, Xiaohong; Shen, Licheng; Wu, Kunyu; Huang, Mingzhi; Xiao, Qiong

2016-06-01

Mapamyum geothermal field (MGF) in western Tibet is one of largest geothermal areas characterized by the occurrence of hydrothermal explosions on the Tibetan Plateau. The geochemical properties of hydrothermal water in the MGF system were investigated to trace the origin of the solutes and to determine the equilibrium temperatures of the feeding reservoir. The study results show that the geochemistry of hydrothermal waters in the MGF system is mainly of the Na-HCO3 type. The chemical components of hydrothermal waters are mainly derived from the minerals in the host rocks (e.g., K-feldspar, albite, Ca-montmorillonite, and Mg-montmorillonite). The hydrothermal waters are slightly supersaturated or undersaturated with respect to aragonite, calcite, dolomite, chalcedony and quartz (saturation indices close to 0), but are highly undersaturated with respect to gypsum and anhydrite (saturation indices < 0). Mixing models and Na-K-Mg ternary diagrams show that strong mixing between cold meteoric water and deeply-seated thermal fluids occurred during the upward flowing process. δD and δ18O data confirm that the meteoric water acts as the water source of the geothermal waters. An 220 °C equilibrated reservoir temperature of hydrothermal spring waters was calculated via both the Na-K-Mg ternary diagrams and the cationic chemical geothermometers. The logpCO2 of hydrothermal waters in the MGF system ranges from - 2.59 to - 0.57 and δ13C of the total dissolved inorganic carbon ranges from - 5.53‰ to - 0.94‰, suggesting that the carrier CO2 in hydrothermal water are mainly of a magmatic or metamorphic CO2 origin.

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

NASA Astrophysics Data System (ADS)

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.

The bulk isotopic composition of hydrocarbons in subaerial volcanic-hydrothermal emissions from different tectonic settings

NASA Astrophysics Data System (ADS)

Fiebig, J.; Tassi, F.; Vaselli, O.; Viveiros, M. F.; Silva, C.; Lopez, T. M.; D'Alessandro, W.; Stefansson, A.

2015-12-01

Assuming that methane and its higher chain homologues derive from a common source, carbon isotope patterns have been applied as a criterion to identify occurrences of abiogenic hydrocarbons. Based on these, it has been postulated that abiogenic hydrocarbon production occurs within several (ultra)mafic environments. More evolved volcanic-hydrothermal systems may also provide all the prerequisites necessary for abiogenic hydrocarbon production, such as availability of inorganic CO2, hydrogen and heat. We have investigated the chemical and isotopic composition of n-alkanes contained within subaerial hydrothermal discharges emitted from a range of hot spot, subduction and rift-related volcanoes to determine the origin of hydrocarbons in these systems. Amongst these are Nisyros (Greece), Vesuvio, Campi Flegrei, Ischia, Pantelleria and Vulcano (all Italy), Mt. Mageik and Trident (USA), Copahue (Argentina), Teide (Spain), Furnas and Fogo (Portugal). The carbon isotopic composition of methane emitted from these sites varies from -65 to -8‰ , whereas δ13C of ethane and propane exhibit a much narrower variation from -17‰ to -31‰. Methane that occurs most enriched in 13C is also characterized by relatively positive δD values ranging up to -80‰. Carbon isotope reversals between methane and ethane are only observed for locations exhibiting δ13C-CH4 values > -20‰, such as Teide, Pantelleria, Trident and Furnas. At Furnas, δ13C-CH4 varies by 50‰ within a relatively short distance of <50m between two vents, whereas δ13C-C2H6 varies by less than 2‰ only. For some of the investigated locations apparent carbon isotopic temperatures between methane and CO2 are in agreement with those derived from gas concentration geothermometers. At these locations methane, however seems to be in disequilibrium with ethane and propane. These findings imply that methane on the one hand and the C2+ hydrocarbons on the other hand often might derive from distinct sources.

Occurrence of Tourmaline in Metasedimentary Rocks of the Isua Supracrustal Belt, Greenland: Implications for Ribose Stabilization in Hadean Marine Sediments.

PubMed

Mishima, Shinpei; Ohtomo, Yoko; Kakegawa, Takeshi

2016-06-01

Abiotic formation of RNA was important for the emergence of terrestrial life, but the acknowledged difficulties of generating and stabilizing ribose have often raised questions regarding how the first RNA might have formed. Previous researchers have proposed that borate could have stabilized ribose; however, the availability of borate on the early Earth has been the subject of intense debate. In order to examine whether borate was available on the early Earth, this study examined metasedimentary rocks from the Isua Supracrustal Belt. Garnet, biotite, and quartz comprise the major constituents of the examined rocks. Field relationships and the chemical compositions of the examined rocks suggest sedimentary origin. The present study found that garnet crystals contain a number of inclusions of tourmaline (a type of borosilicate mineral). All tourmaline crystals are Fe-rich and categorized as schorl. Both garnet and tourmaline often contain graphite inclusions and this close association of tourmaline with garnet and graphite has not been recognized previously. Garnet-biotite and graphite geothermometers suggest that the tourmaline in garnet experienced peak metamorphic conditions (~500 °C and 5 kbar). The mineralogical characteristics of the tourmaline and the whole rock composition indicate that the tourmaline formed authigenically in the sediment during diagenesis and/or early metamorphism. Clay minerals in modern sediments have the capability to adsorb and concentrate borate, which could lead to boron enrichment during diagenesis, followed by tourmaline formation under metamorphic conditions. Clay minerals, deposited on the early Archean seafloor, were the precursors of the garnet and biotite in the examined samples. The studied tourmaline crystals were most likely formed in the same way as modern tourmaline in marine sediments. Therefore, boron enrichment by clays must have been possible even during the early Archean. Thus, similar enrichment could have been possible during the Hadean, providing a stabilization agent for ribose.

An Excel-based tool for evaluating and visualizing geothermobarometry data

NASA Astrophysics Data System (ADS)

Hora, John Milan; Kronz, Andreas; Möller-McNett, Stefan; Wörner, Gerhard

2013-07-01

Application of geothermobarometry based on equilibrium exchange of chemical components between two mineral phases in natural samples frequently leads to the dilemma of either: (1) relying on relatively few measurements where there is a high likelihood of equilibrium, or (2) using many analysis pairs, where a significant proportion may not be useful and must be filtered out. The second approach leads to the challenges of (1) evaluation of equilibrium for large numbers of analysis pairs, (2) finding patterns in the dataset where multiple populations exist, and (3) visualizing relationships between calculated temperatures and compositional and textural parameters. Given the limitations of currently-used thermobarometry spreadsheets, we redesign them in a way that eliminates tedium by automating data importing, quality control and calculations, while making all results visible in a single view. Rather than using a traditional spreadsheet layout, we array the calculations in a grid. Each color-coded grid node contains the calculated temperature result corresponding to the intersection of two analyses given in the corresponding column and row. We provide Microsoft Excel templates for some commonly-used thermometers, that can be modified for use with any geothermometer or geobarometer involving two phases. Conditional formatting and ability to sort according to any chosen parameter simplifies pattern recognition, while tests for equilibrium can be incorporated into grid calculations. A case study of rhyodacite domes at Parinacota volcano, Chile, indicates a single population of Fe-Ti oxide temperatures, despite Mg-Mn compositional variability. Crystal zoning and differing thermal histories are, however, evident as a bimodal population of plagioclase-amphibole temperatures. Our approach aids in identification of suspect analyses and xenocrysts and visualization of links between temperature and phase composition. This facilitates interpretation of whether heat transfer was accompanied by bulk mass transfer, and to what degree diffusion has homogenized calculated temperature results in hybrid magmas.

Reconstruction of limnology and microbialite formation conditions from carbonate clumped isotope thermometry.

PubMed

Petryshyn, V A; Lim, D; Laval, B L; Brady, A; Slater, G; Tripati, A K

2015-01-01

Quantitative tools for deciphering the environment of microbialite formation are relatively limited. For example, the oxygen isotope carbonate-water geothermometer requires assumptions about the isotopic composition of the water of formation. We explored the utility of using 'clumped' isotope thermometry as a tool to study the temperatures of microbialite formation. We studied microbialites recovered from water depths of 10-55 m in Pavilion Lake, and 10-25 m in Kelly Lake, spanning the thermocline in both lakes. We determined the temperature of carbonate growth and the (18)O/(16)O ratio of the waters that microbialites grew in. Results were then compared to current limnological data from the lakes to reconstruct the history of microbialite formation. Modern microbialites collected at shallow depths (11.7 m) in both lakes yield clumped isotope-based temperatures of formation that are within error of summer water temperatures, suggesting that clumped isotope analyses may be used to reconstruct past climates and to probe the environments in which microbialites formed. The deepest microbialites (21.7-55 m) were recovered from below the present-day thermoclines in both lakes and yield radioisotope ages indicating they primarily formed earlier in the Holocene. During this time, pollen data and our reconstructed water (18)O/(16)O ratios indicate a period of aridity, with lower lake levels. At present, there is a close association between both photosynthetic and heterotrophic communities, and carbonate precipitation/microbialite formation, with biosignatures of photosynthetic influences on carbonate detected in microbialites from the photic zone and above the thermocline (i.e., depths of generally <20 m). Given the deeper microbialites are receiving <1% of photosynthetically active radiation (PAR), it is likely these microbialites primarily formed when lower lake levels resulted in microbialites being located higher in the photic zone, in warm surface waters. © 2014 John Wiley & Sons Ltd.

Fluid inclusion gas chemistry as a potential minerals exploration tool: Case studies from Creede, CO, Jerritt Canyon, NV, Coeur d'Alene district, ID and MT, southern Alaska mesothermal veins, and mid-continent MVT's

USGS Publications Warehouse

Landis, G.P.; Hofstra, A.H.

1991-01-01

Recent advances in instrumentation now permit quantitative analysis of gas species from individual fluid inclusions. Fluid inclusion gas data can be applied to minerals exploration empirically to establish chemical (gas composition) signatures of the ore fluids, and conceptually through the development of genetic models of ore formation from a framework of integrated geologic, geochemical, and isotopic investigations. Case studies of fluid inclusion gas chemistry from ore deposits representing a spectrum of ore-forming processes and environments are presented to illustrate both the empirical and conceptual approaches. We consider epithermal silver-gold deposits of Creede, Colorado, Carlin-type sediment-hosted disseminated gold deposits of Jerritt Canyon, Nevada, metamorphic silver-base-metal veins of the Coeur d'Alene district, Idaho and Montana, gold-quartz veins in accreted terranes of southern Alaska, and the mid-continent base-metal sulfide deposits of Mississippi Valley-Type (MVT's). Variations in gas chemistry determine the redox state of the ore fluids, provide compositional input for gas geothermometers, characterize ore fluid chemistry (e.g., CH4CO2, H2SSO2, CO2/H2S, organic-rich fluids, gas-rich and gas-poor fluids), identify magmatic, meteoric, metamorphic, shallow and deep basin fluids in ore systems, locate upwelling plumes of magmatic-derived volatiles, zones of boiling and volatile separation, interfaces between contrasting fluids, and important zones of fluid mixing. Present techniques are immediately applicable to exploration programsas empirical studies that monitor fluid inclusion gas threshold concentration levels, presence or absence of certain gases, or changes in gas ratios. We suggest that the greater contribution of fluid inclusion gas analysis is in the integrated and comprehensive chemical dimension that gas data impart to genetic models, and in the exploration concepts based on processes and environments of ore formation derived from these genetic models. ?? 1991.

Development of the archean crust in the medina mountain area, wind river range, wyoming (U.S.A.)

USGS Publications Warehouse

Koesterer, M.E.; Frost, C.D.; Frost, B.R.; Hulsebosch, T.P.; Bridgwater, D.; Worl, R.G.

1987-01-01

Evidence for an extensive Archean crustal history in the Wind River Range is preserved in the Medina Mountain area in the west-central part of the range. The oldest rocks in the area are metasedimentary, mafic, and ultramafic blocks in a migmatite host. The supracrustal rocks of the Medina Mountain area (MMS) are folded into the migmatites, and include semi-pelitic and pelitic gneisses, and mafic rocks of probable volcanic origin. Mafic dikes intrude the older migmatites but not the MMS, suggesting that the MMS are distinctly younger than the supracrustal rocks in the migmatites. The migmatites and the MMS were engulfed by the late Archean granite of the Bridger, Louis Lake, and Bears Ears batholiths, which constitutes the dominant rock of the Wind River Range. Isotopic data available for the area include Nd crustal residence ages from the MMS which indicate that continental crust existed in the area at or before 3.4 Ga, but the age of the older supracrustal sequence is not yet known. The upper age of the MMS is limited by a 2.7 Ga RbSr age of the Bridger batholith, which was emplaced during the waning stages of the last regional metamorphism. The post-tectonic Louis Lake and Bears Ears batholiths have ages of 2.6 and 2.5 Ga, respectively (Stuckless et al., 1985). At least three metamorphic events are recorded in the area: (1) an early regional granulite event (M1) that affected only the older inclusions within the migmatites, (2) a second regional amphibolite event (M2) that locally reached granulite facies conditions, and (3) a restricted, contact granulite facies event (M3) caused by the intrusion of charnockitic melts associated with the late Archean plutons. Results from cation exchange geobarometers and geothermometers yield unreasonablu low pressures and temperatures, suggesting resetting during the long late Archean thermal evenn. ?? 1987.

Thermally induced cation redistribution in Fe-bearing oxy-dravite and potential geothermometric implications

NASA Astrophysics Data System (ADS)

Bosi, Ferdinando; Skogby, Henrik; Hålenius, Ulf

2016-05-01

Iron-bearing oxy-dravite was thermally treated in air and hydrogen atmosphere at 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 intersite geothermometry based on tourmaline. Overall, the experimental data (structural refinement, Mössbauer, infrared and optical absorption spectroscopy) show that heating Fe-bearing tourmalines results in disordering of Fe over Y and Z balanced by ordering of Mg at Y, whereas Al does not change appreciably. The Fe disorder depends on temperature, but less on redox conditions. The degree of Fe3+-Fe2+ reduction is limited despite strongly reducing conditions, indicating that the f O2 conditions do not exclusively control the Fe oxidation state at the present experimental conditions. Untreated and treated samples have similar short- and long-range crystal structures, which are explained by stable Al-extended clusters around the O1 and O3 sites. In contrast to the stable Al clusters that preclude any temperature-dependent Mg-Al order-disorder, there occurs Mg diffusion linked to temperature-dependent exchange with Fe. Ferric iron mainly resides around O2- at O1 rather than (OH)-, but its intersite disorder induced by thermal treatment indicates that Fe redistribution is the driving force for Mg-Fe exchange and that its diffusion rates are significant at these temperatures. With increasing temperature, Fe progressively disorders over Y and Z, whereas Mg orders at Y according to the order-disorder reaction: YFe + ZMg → ZFe + YMg. The presented findings are important for interpretation of the post-crystallization history of both tourmaline and tourmaline host rocks and imply that successful tourmaline geothermometers may be developed by thermal calibration of the Mg-Fe order-disorder reaction, whereas any thermometers based on Mg-Al disorder will be insensitive and involve large uncertainties.

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

NASA Astrophysics Data System (ADS)

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.

Raman spectra of carbonaceous materials in a fault zone in the Longmenshan thrust belt, China; comparisons with those of sedimentary and metamorphic rocks

NASA Astrophysics Data System (ADS)

Kouketsu, Yui; Shimizu, Ichiko; Wang, Yu; Yao, Lu; Ma, Shengli; Shimamoto, Toshihiko

2017-03-01

We analyzed micro-Raman spectra of carbonaceous materials (CM) in natural and experimentally deformed fault rocks from Longmenshan fault zone that caused the 2008 Wenchuan earthquake, to characterize degree of disordering of CM in a fault zone. Raman spectral parameters for 12 samples from a fault zone in Shenxigou, Sichuan, China, all show low-grade structures with no graphite. Low crystallinity and δ13C values (-24‰ to -25‰) suggest that CM in fault zone originated from host rocks (Late Triassic Xujiahe Formation). Full width at half maximum values of main spectral bands (D1 and D2), and relative intensities of two subbands (D3 and D4) of CM were variable with sample locations. However, Raman parameters of measured fault rocks fall on established trends of graphitization in sedimentary and metamorphic rocks. An empirical geothermometer gives temperatures of 160-230 °C for fault rocks in Shenxigou, and these temperatures were lower for highly sheared gouge than those for less deformed fault breccia at inner parts of the fault zone. The lower temperature and less crystallinity of CM in gouge might have been caused by the mechanical destruction of CM by severe shearing deformation, or may be due to mixing of host rocks on the footwall. CM in gouge deformed in high-velocity experiments exhibits slight changes towards graphitization characterized by reduction of D3 and D4 intensities. Thus low crystallinity of CM in natural gouge cannot be explained by our experimental results. Graphite formation during seismic fault motion is extremely local or did not occur in the study area, and the CM crystallinity from shallow to deep fault zones may be predicted as a first approximation from the graphitization trend in sedimentary and metamorphic rocks. If that case, graphite may lower the friction of shear zones at temperatures above 300 °C, deeper than the lower part of seismogenic zone.

Physical characteristics and quality of water from selected springs and wells in the Lincoln Point-Bird Island area, Utah Lake, Utah

USGS Publications Warehouse

Baskin, R.L.; Spangler, L.E.; Holmes, W.F.

1994-01-01

From February 1991 to October 1992, the U.S. Geological Survey, in cooperation with the Central Utah Water Conservancy District, investigated the hydrology of the Lincoln Point - Bird Island area in the southeast part of Utah Lake, Utah. The investigation included measurements of the discharge of selected springs and measurements of the physical and chemical characteristics of water from selected springs and wells in the LincolnPoint - Bird Island area. This report contains data for twenty-one distinct springs in the study area including two springs beneath the surface of Utah Lake at Bird Island. Data from this study, combined with data from previous studies, indicate that the location of springs in the Lincoln Point - Bird Island area probably is controlled by fractures that are the result of faulting. Measured discharge of springs in the Lincoln Point - Bird Island area ranged from less than 0.01 cubic foot per second to 0.84 cubic foot per second. Total discharge in the study area, including known unmeasured springs and seeps, is estimated to be about 5 cubic feet per second. Reported and measured temperatures of water from springs and wells in the Lincoln Point - Bird Island area ranged from 16.0 degrees Celsius to 36.5 degrees Celsius. Dissolved-solids con-centrations ranged from 444 milligrams per liter to 7,932 milligrams per liter, and pH ranged from 6.3 to 8.1. Physical and chemical characteristics of spring and well water from the west side of Lincoln Point were virtually identical to the physical and chemical characteristics of water from the submerged Bird Island springs, indicating a similar source for the water. Water chemistry, isotope analyses, and geothermometer calculations indicate deep circulation of water discharging from the springs and indicate that the source of recharge for the springs at Lincoln Point and Bird Island does not appear to be localized in the LincolnPoint - Bird Island area.

Geothermal Modeling of the Karoo Basin, South Africa, using Rock Magnetic Methods

NASA Astrophysics Data System (ADS)

Maré, L.; de Kock, M.; Cairncross, B.; Mouri, H.; Ferre, E. C.; Jackson, M. J.

2014-12-01

The viability of using magnetic fabric analyses as geothermometers in sedimentary basins was investigated and new constraints on regional-scale geotherms for the Karoo sedimentary Basin were identified. A comparative study of the variation in magnetic properties in eight boreholes located along a southwest to northeast traverse across the Karoo Basin was performed. The thermal impact of the intrusive Karoo Dolerite Suite on the surrounding sediments was determined using several magnetic experiments. The methods employed during the investigation include low field anisotropy of magnetic susceptibility, variation in magneto-stratigraphy using the classic baked contact test, the magnetic Alteration Index (A40) as well as looking at the possibility to use magnetite-pyrrhotite geothermometry.The experiments indicated the heating effect of the dolerite intrusions to be limited to short distances within the contact aureole. Boreholes that intersected dolerite sills indicated that the heating effect occurred no wider than half the sill thicknesses. However, due to the extensive network of sills and dykes in the Karoo Basin, an overall elevation in the geomagnetic temperatures of the stratigraphic sequence to temperatures above 150 °C was observed. This knowledge could have major implications for any potential shale-gas industry in South Africa.Temperatures calculated by the A40 method (minimum observed values) indicated a general increase from southwest to northeast in the thermal effect of intrusions on the Karoo sediments. This correlates with reported increased coal maturity from west to east. Several hypotheses exist for this geothermal variation including the influence that distance to magma source might have had. The most probable hypothesis however, relates to the different environmental settings that prevailed between the western and eastern parts of the basin during magma intrusion and the associated differences in thermal conductivity of low permeable marine shale in the west compared to the porous lacustrine sandstone and siltstone towards the east.

Stabilization of kerogen thermal maturation: Evidence from geothermometry and burial history reconstruction, Niobrara Limestone, Berthoud oil field, western Denver Basin, Colorado

DOE Office of Scientific and Technical Information (OSTI.GOV)

Barker, C.E.; Crysdale, B.L.

1990-05-01

The burial history of this fractured Niobrara Limestone reservoir and source rock offers a setting for studying the stabilization of thermal maturity because soon after peak temperature of approximately 100{degree}C was reached, exhumation lowered temperature to about 60-70{degree}C. Vitrinite reflectance (Rm = 0.6-0.7%) and published clay mineralogy data from the Niobrara Limestone indicate that peak paleotemperature was approximately 100{degree}C. Fluid inclusion data also indicate oil migration occurred at 100{degree}C. Burial history reconstruction indicates 100{degree}C was reached in the Niobrara Limestone only during minimum burial, which occurred at 70 Ma and 8000 ft depth. However, erosion beginning at 70 Ma andmore » continuing until 50 Ma removed over 3,000 ft of rock. This depth of erosion agrees with an Rm of 0.4% measured in surface samples of the Pierre Shale. The exhumation of the reservoir decreased temperature by about 30{degree}C to near the corrected bottom-hole temperature of 50-70{degree}C. Lopatin time-temperature index (TTI) analysis suggests the Niobrara Limestone as a source rock matured to the oil generation stage (TTI = 10) about 25 Ma, significantly later than maximum burial, and after exhumation caused cooling. The Lopatin TTI method in this case seems to overestimate the influence of heating time. If time is an important factor, thermal maturity should continue to increase after peak burial and temperature so that vitrinite reflectance will not be comparable to peak paleotemperatures estimated from geothermometers set at near-peak temperature and those estimated from burial history reconstruction. The agreement between geothermometry and the burial history reconstruction in Berthoud State 4 suggests that the influence of heating time must be small. The elapsed time available at near peak temperatures was sufficient to allow stabilization of thermal maturation in this case.« less

Magmatic-hydrothermal fluid interaction and mineralization in alkali-syenite nodules from the Breccia Museo pyroclastic deposit, Naples, Italy: Chapter 7 in Volcanism in the Campania Plain — Vesuvius, Campi Flegrei and Ignimbrites

USGS Publications Warehouse

Fedele, Luca; Tarzia, Maurizio; Belkin, Harvey E.; De Vivo, Benedetto; Lima, Annamaria; Lowenstern, Jacob

2007-01-01

The Breccia Museo, a pyroclastic flow that crops out in the Campi Flegrei volcanic complex (Naples, Italy), contains alkali-syenite (trachyte) nodules with enrichment in Cl and incompatible elements (e.g., U, Zr, Th, and rare-earth elements). Zircon was dated at ≈52 ka, by U-Th isotope systematics using a SHRIMP. Scanning electron microscope and electron microprobe analysis of the constituent phases have documented the mineralogical and textural evolution of the nodules of feldspar and mafic accumulations on the magma chamber margins. Detailed electron microprobe data are given for alkali and plagioclase feldspar, salite to ferrosalite clinopyroxene, pargasite, ferrogargasite, magnesio-hastingsite hornblende amphibole, biotite mica, Cl-rich scapolite, and a member (probable davyne-type) of the cancrinite group. Detailed whole rock, major and minor element data are also presented for selected nodules. A wide variety of common and uncommon accessory minerals were identified such as zircon, baddeleyite, zirconolite, pollucite, sodalite, titanite, monazite, cheralite, apatite, titanomagnetite and its alteration products, scheelite, ferberite, uraninite/thorianite, uranpyrochlore, thorite, pyrite, chalcopyrite, and galena. Scanning electron microscope analysis of opened fluid inclusions identified halite, sylvite, anhydrite, tungstates, carbonates, silicates, sulfides, and phosphates; most are probably daughter minerals. Microthermometric determinations on secondary fluid inclusions hosted by alkali feldspar define a temperature regime dominated by hypersaline aqueous fluids. Fluid-inclusion temperature data and mineral-pair geothermometers for coexisting feldspars and hornblende and plagioclase were used to construct a pressure-temperature scenario for the development and evolution of the nodules. We have compared the environment of porphyry copper formation and the petrogenetic environment constructed for the studied nodules. The suite of ore minerals observed in the nodules supports a potential for mineralization, which is similar to that observed in the alkaline volcanic systems of southern Italy (Pantelleria, Pontine Archipelago, Mt. Somma-Vesuvius).

On the Future of Thermochemical Databases, the Development of Solution Models and the Practical Use of Computational Thermodynamics in Volcanology, Geochemistry and Petrology: Can Innovations of Modern Data Science Democratize an Oligarchy?

NASA Astrophysics Data System (ADS)

Ghiorso, M. S.

2014-12-01

Computational thermodynamics (CT) has now become an essential tool of petrologic and geochemical research. CT is the basis for the construction of phase diagrams, the application of geothermometers and geobarometers, the equilibrium speciation of solutions, the construction of pseudosections, calculations of mass transfer between minerals, melts and fluids, and, it provides a means of estimating materials properties for the evaluation of constitutive relations in fluid dynamical simulations. The practical application of CT to Earth science problems requires data. Data on the thermochemical properties and the equation of state of relevant materials, and data on the relative stability and partitioning of chemical elements between phases as a function of temperature and pressure. These data must be evaluated and synthesized into a self consistent collection of theoretical models and model parameters that is colloquially known as a thermodynamic database. Quantitative outcomes derived from CT reply on the existence, maintenance and integrity of thermodynamic databases. Unfortunately, the community is reliant on too few such databases, developed by a small number of research groups, and mostly under circumstances where refinement and updates to the database lag behind or are unresponsive to need. Given the increasing level of reliance on CT calculations, what is required is a paradigm shift in the way thermodynamic databases are developed, maintained and disseminated. They must become community resources, with flexible and assessable software interfaces that permit easy modification, while at the same time maintaining theoretical integrity and fidelity to the underlying experimental observations. Advances in computational and data science give us the tools and resources to address this problem, allowing CT results to be obtained at the speed of thought, and permitting geochemical and petrological intuition to play a key role in model development and calibration.

Constraints of C-O-S isotope compositions and the origin of the Ünlüpınar volcanic-hosted epithermal Pb-Zn ± Au deposit, Gümüşhane, NE Turkey

NASA Astrophysics Data System (ADS)

Akaryali, Enver; Akbulut, Kübra

2016-03-01

The Eastern Pontide Orogenic Belt (EPOB) constitutes one of the best examples of the metallogenic provinces in on the Alpine-Himalayan belt. This study focuses on the genesis of the Ünlüpınar Pb-Zn ± Au deposit in the southern part of the Eastern Pontide Orogenic Belt. The main lithological units in the study area are the Early Carboniferous Kurtoğlu Metamorphic Complex the Late Carboniferous Köse Granitoid and the Early-Middle Jurassic Şenköy Formation. The studied deposit is hosted by the Şenköy Formation, which consists predominantly of basaltic-andesitic rocks and associated pyroclastic rocks that are calc-alkaline in composition. Silicic, sulfidic, argillic, chloritic, hematitic, carbonate and limonite are the most obvious alteration types observed in the deposit site. Ore microscopy studies exhibit that the mineral paragenesis in deposits includes pyrite, chalcopyrite, sphalerite, galena, gold, quartz and calcite. Electron microprobe analyses conducted on sphalerite indicate that the Zn/Cd ratio varies between 84 and 204, and these ratios point at a hydrothermal deposit related to granitic magmas. Fluid inclusion studies in calcite and quartz show that the homogenization temperature of the studied deposit ranges between 90-160 °C and 120-330 °C respectively. The values of sulfur isotope analysis of pyrite, sphalerite and galena minerals vary between 1.6‰ and 5.7‰, and the results of oxygen and carbon isotope analysis range between 8.4‰ and 18‰ and -5‰ and -3.6‰, respectively. The average formation temperature of the ore was calculated as 264 °C with a sulfur isotope geothermometer. All of the data indicate that the Ünlüpınar deposit is an epithermal vein-type mineralization that was formed depending on the granitic magmatism.

A reconnaissance geochemical study of La Primavera geothermal area, Jalisco, Mexico

USGS Publications Warehouse

Mahood, G.A.; Truesdell, A.H.; Templos, M.L.A.

1983-01-01

The Sierra La Primavera, a late Pleistocene rhyolitic caldera complex in Jalisco, Me??xico, contains fumaroles and large-discharge 65??C hot springs that are associated with faults related to caldera collapse and to later magma insurgence. The nearly-neutral, sodium bicarbonate, hot springs occur at low elevations at the margins of the complex, whereas the water-rich fumaroles are high and central. The Comisio??n Federal de Electricidad de Me??xico (CFE) has recently drilled two deep holes at the center of the Sierra (PR-1 and Pr-2) and one deep hole at the western margin. Temperatures as high as 285??C were encountered at 1160 m in PR-1, which produced fluids with 820 to 865 mg/kg chloride after flashing to one atmosphere. Nearby, PR-2 encountered temperatures to 307??C at 2000 m and yielded fluids with chloride contents fluctuating between 1100 and 1560 mg/kg after flashing. Neither of the high-temperature wells produced steam in commercial quantities. The well at the western margin of the Sierra produced fluids similar to those from the hot springs. The temperature reached a maximum of 100??C near the surface and decreased to 80??C at 2000 m. Various geothermometers (quartz conductive, Na/K, Na-K-Ca, ??18O(SO4-H2O) and D/H (steam-water) all yield temperatures of 170 ?? 20??C when applied to the hot spring waters, suggesting that these spring waters flow from a large shallow reservoir at this temperature. Because the hot springs are much less saline than the fluids recovered in PR-1 and PR-2, the mixed fluid in the shallow reservoir can contain no more than 10-20% deep fluid. This requires that most of the heat is transferred by steam. There is probably a thin vapor-dominated zone in the central part of the Sierra, through which steam and gases are transferred to the overlying shallow reservoir. Fluids from this reservoir cool from ???170??C to 65??C by conduction during the 5-7 km of lateral flow to the hot springs. ?? 1983.

Petrogenetic grids for sapphirine-bearing granulites

NASA Astrophysics Data System (ADS)

Podlesskii, Konstantin K.

2010-05-01

Phase relations involving sapphirine, garnet, spinel, orthopyroxene, olivine, cordierite, alumina silicates, corundum, and quartz have been calculated in the system FeO-MgO-Al2O3-SiO2 based on internally consitent thermodynamic properties of both the end-member minerals and the solid solutions (Gerya et al., 2004; Podlesskii et al., 2008). The derived P-T diagrams imply stable invariant points and stability fields of key assemblages that differ from those proposed by other authors (Kelsey et al., 2004; Harley 2008). The sapphirine + quartz assemblage, which is widely recognized as indicative of ultrahigh-temperature metamorphism, can be stable down to 835° C and ~6 kbar. The sapphirine + kyanite assemblage has been found stable at temperatures below 860° C and 11.3 kbar, whereas the sapphirine + forsterite assemblage may be stable below 800° C only under specific conditions of a very low activity of water. The existing constraints on the thermodynamic properties of sapphirine are considered insufficient to make decisive conclusions about metamorphic conditions. Granulites containing the sapphirine + quartz assemblage have been investigated with the microprobe to apply both the conventional thermobarometry and thermometry based on Ti contents of quartz (TitaniQ, Wark & Watson, 2006). The results demonstrate that, in some cases, this assemblage might have formed at relatively low temperatures during retrograde stages of metamorphism. The research has been supported by the RFBR grant 09-05-00193. References Gerya,T.V., Perchuk,L.L., & Podlesskii,K.K. In: Zharikov,V.A. & Fed'kin,V.V. (eds.) Experimental Mineralogy: Some Results on the Century's Frontier. Moscow: Nauka, Vol. 2, 188-206 (2004). Harley,S.L. Refining the P-T records of UHT crustal metamorphism. Journal of Metamorphic Geology, 26, 125-154 (2008). Kelsey,D.E., White,R.W., Holland,T.J.B., & Powell,R. Journal of Metamorphic Geology, 22, 559-578 (2004). Podlesskii,K.K., Aranovich,L.Y., Gerya,T.V., & Kosyakova,N.A. Sapphirine-bearing assemblages in the system MgO-Al2O3-SiO2: A continuing ambiguity. European Journal of Mineralogy, 20, 721-734 (2008). Wark,D.A. & Watson,E.B. TitaniQ: a titanium-in-quartz geothermometer. Contributions to Mineralogy and Petrology, 152, 743-754 (2006).

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

NASA Astrophysics Data System (ADS)

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 strong limitation to the exploitation of this geothermal resource, the occurrence of Li- and Ba-rich deposits associated with the hydrothermal fluids may attract financial investments, giving a pulse for the development of this remote region.

Chemical indicators of subsurface temperature applied to hot spring waters of Yellowstone National Park, Wyoming, U.S.A.

USGS Publications Warehouse

Fournier, R.O.; Truesdell, A.H.

1970-01-01

Under favorable conditions the chemistry of hot springs may give reliable indications of subsurface temperatures and circulation patterns. These chemical indicators can be classified by the type of process involved: {A table is presented}. All these indicators have certain limitations. The silica geothermometer gives results independent of the local mineral suite and gas partial pressures, but may be affected by dilution. Alkali ratios are strongly affected by the local mineral suite and the formation of complex ions. Carbonate-chloride ratios are strongly affected by subsurface PCO2. The relative concentration of volatiles can be very misleading in high-pressure liquid systems. In Yellowstone National Park most thermal waters issue from hot, shallow aquifers with pressures in excess of hydrostatic by 2 to 6 bars and with large flows (the flow of hot spring water from the Park is greater than 4000 liters per second). These conditions should be ideal for the use of chemical indicators to estimate aquifer temperatures. In five drill holes aquifer temperatures were within 2??C of that predicted from the silica content of nearby hot springs; the temperature level off at a lower value than predicted in only one hole, and in four other holes drilling was terminated before the predicted aquifer temperature was reached. The temperature-Na/K ratio relationship does not follow any published experimental or empirical curve for water-feldspar or water-clay reactions. We suspect that ion exchange reactions involving zeolites in the Yellowstone rocks result in higher Na/K ratios at given temperatures than result from feldspar or clay reactions. Comparison of SiO2 and Cl/(HCO3 + CO3) suggest that because of higher subsurface PCO2 in Upper Geyser Basin a given Cl/(HCO3 + CO3) ratio there means a higher temperature than in Lower Geyser Basin. No correlation was found in Yellowstone Park between the subsurface regions of highest temperature and the relative concentration of volatile components such as boron and ammonia. ?? 1971.

LEPER: Library of Experimental PhasE Relations

NASA Astrophysics Data System (ADS)

Davis, F.; Gordon, S.; Mukherjee, S.; Hirschmann, M.; Ghiorso, M.

2006-12-01

The Library of Experimental PhasE Relations (LEPER) seeks to compile published experimental determinations of magmatic phase equilibria and provide those data on the web with a searchable and downloadable interface. Compiled experimental data include the conditions and durations of experiments, the bulk compositions of experimental charges, and the identity, compositions and proportions of phases observed, and, where available, estimates of experimental and analytical uncertainties. Also included are metadata such as the type of experimental device, capsule material, and method(s) of quantitative analysis. The database may be of use to practicing experimentalists as well as the wider Earth science community. Experimentalists may find the data useful for planning new experiments and will easily be able to compare their results to the full body of previous experimentnal data. Geologists may use LEPER to compare rocks sampled in the field with experiments performed on similar bulk composition or with experiments that produced similar-composition product phases. Modelers may use LEPER to parameterize partial melting of various lithologies. One motivation for compiling LEPER is for calibration of updated and revised versions of MELTS, however, it is hoped that the availability of LEPER will facilitate formulation and calibration of additional thermodynamic or empirical models of magmatic phase relations and phase equilibria, geothermometers and more. Data entry for LEPER is occuring presently: As of August, 2006, >6200 experiments have been entered, chiefly from work published between 1997 and 2005. A prototype web interface has been written and beta release on the web is anticipated in Fall, 2006. Eventually, experimentalists will be able to submit their new experimental data to the database via the web. At present, the database contains only data pertaining to the phase equilibria of silicate melts, but extension to other experimental data involving other fluids or sub-solidus phase equilibria may be contemplated. Also, the data are at present limited to natural or near-natural systems, but in the future, extension to synthetic (i.e., CMAS, etc.) systems is also possible. Each would depend in part on whether there is community demand for such databases. A trace element adjunct to LEPER is presently in planning stages.

A Gradient in Cooling Rate Beneath the Moho at the Oman Ophiolite: Fresh Insights into Cooling Processes at Mid-Ocean Ridges from REE-Based Thermometry

NASA Astrophysics Data System (ADS)

Dygert, N. J.; Kelemen, P. B.; Liang, Y.

2015-12-01

The Wadi Tayin massif in the southern Oman ophiolite has a more than 10 km thick mantle section and is believed to have formed in a mid-ocean ridge like environment with an intermediate to fast spreading rate. Previously, [1] used major element geothermometers to investigate spatial variations in temperatures recorded in mantle peridotites and observed that samples near the paleo-Moho have higher closure temperatures than samples at the base of the mantle section. Motivated by these observations, we measured major and trace elements in orthopyroxene and clinopyroxene in peridotites from depths of ~1-8km beneath the Moho to determine closure temperatures of REE in the samples using the REE-in-two-pyroxene thermometer [2]. Clinopyroxene are depleted in LREE and have REE concentrations that vary depending on distance from the Moho. Samples nearer the Moho have lower REE concentrations than those deeper in the section (e.g., chondrite normalized Yb ranges from ~1.5 at the Moho to 4 at 8km depth), consistent with near fractional melting along a mantle adiabat. Orthopyroxene are highly depleted in LREE but measurements of middle to heavy REE have good reproducibility. We find that REE-in-two-pyroxene temperatures decrease with increasing distance from the Moho, ranging from 1325±10°C near the Moho to 1063±24°C near the base of the mantle section. Using methods from [3], we calculate cooling rates of >1000°C/Myr near the Moho, dropping to rates of <10°C/Myr at the bottom of the section. The faster cooling rate is inconsistent with conductive cooling models. Fast cooling of the mantle lithosphere could be facilitated by infiltration of seawater to or beneath the petrologic Moho. This can explain why abyssal peridotites from ultra-slow spreading centers (which lack a crustal section) have cooling rates comparable to those of Oman peridotites [3]. [1] Hanghøj et al. (2010), JPet 51(1-2), 201-227. [2] Liang et al. (2013), GCA 102, 246-260. [3] Dygert & Liang (2015), EPSL 420, 151-161.

The temperature of primary melts and mantle sources of komatiites, OIBs, MORBs and LIPs

NASA Astrophysics Data System (ADS)

Sobolev, Alexander

2015-04-01

There is general agreement that the convecting mantle, although mostly peridotitic in composition, is compositionally and thermally heterogeneous on different spatial scales. The amount, sizes, temperatures and compositions of these heterogeneities significantly affect mantle dynamics because they may diverge greatly from dominant peridotites in their density and fusibility. Differences in potential temperature and composition of mantle domains affect magma production and cannot be easily distinguished from each other. This has led to radically different interpretations of the melting anomalies that produce ocean-island basalts, large igneous provinces and komatiites: most scientists believe that they originate as hot, deep-sourced mantle plumes; but a small though influential group (e.g. Anderson 2005, Foulger, 2010) propose that they derive from high proportions of easily fusible recycled or delaminated crust, or in the case of komatiites contain large amount of H2O (e.g. Grove & Parman, 2004). The way to resolve this ambiguity is an independent estimation of temperature and composition of mantle sources of various types of magma. In this paper I report application of newly developed olivine-spinel-melt geothermometers based on partition of Al, Cr, Sc and Y for different primitive lavas from mid-ocean ridges, ocean-island basalts, large igneous provinces and komatiites. The results suggest significant variations of crystallization temperature for the same Fo of high magnesium olivines of different types of mantle-derived magmas: from the lowest (down to 1220 degree C) for MORB to the highest (up to over 1500 degree C) for komatiites and Siberian meimechites. These results match predictions from Fe-Mg olivine-melt equilibrium and confirm the relatively low temperature of the mantle source of MORB and higher temperatures in the mantle plumes that produce the OIB of Iceland, Hawaii, Gorgona, Archean komatiites and several LIPs (e.g Siberian and NAMP). The established liquidus temperatures and compositions of primary melts allow estimating potential temperatures and compositions of their mantle sources. The results strongly confirm mantle plume theory and presence of variable amounts of recycled crustal material in the mantle sources. This study has been founded by Russian Science Foundation grant 14-17-00491.

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

NASA Astrophysics Data System (ADS)

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 studies of carbonate rocks with thermal history. By contrast, Mg isotopes of dolomite are less prone to post-depositional resetting due to a number of properties including high Mg abundance and high thermodynamic stability, and Mg isotopes in dolomite may be a more robust recorder for original carbonate precipitates.

Equilibrium and non-equilibrium controls on the abundances of clumped isotopologues of methane during thermogenic formation in laboratory experiments: Implications for the chemistry of pyrolysis and the origins of natural gases

NASA Astrophysics Data System (ADS)

Shuai, Yanhua; Douglas, Peter M. J.; Zhang, Shuichang; Stolper, Daniel A.; Ellis, Geoffrey S.; Lawson, Michael; Lewan, Michael D.; Formolo, Michael; Mi, Jingkui; He, Kun; Hu, Guoyi; Eiler, John M.

2018-02-01

Multiply isotopically substituted molecules ('clumped' isotopologues) can be used as geothermometers because their proportions at isotopic equilibrium relative to a random distribution of isotopes amongst all isotopologues are functions of temperature. This has allowed measurements of clumped-isotope abundances to be used to constrain formation temperatures of several natural materials. However, kinetic processes during generation, modification, or transport of natural materials can also affect their clumped-isotope compositions. Herein, we show that methane generated experimentally by closed-system hydrous pyrolysis of shale or nonhydrous pyrolysis of coal yields clumped-isotope compositions consistent with an equilibrium distribution of isotopologues under some experimental conditions (temperature-time conditions corresponding to 'low,' 'mature,' and 'over-mature' stages of catagenesis), but can have non-equilibrium (i.e., kinetically controlled) distributions under other experimental conditions ('high' to 'over-mature' stages), particularly for pyrolysis of coal. Non-equilibrium compositions, when present, lead the measured proportions of clumped species to be lower than expected for equilibrium at the experimental temperature, and in some cases to be lower than a random distribution of isotopes (i.e., negative Δ18 values). We propose that the consistency with equilibrium for methane formed by relatively low temperature pyrolysis reflects local reversibility of isotope exchange reactions involving a reactant or transition state species during demethylation of one or more components of kerogen. Non-equilibrium clumped-isotope compositions occur under conditions where 'secondary' cracking of retained oil in shale or wet gas hydrocarbons (C2-5, especially ethane) in coal is prominent. We suggest these non-equilibrium isotopic compositions are the result of the expression of kinetic isotope effects during the irreversible generation of methane from an alkyl precursor. Other interpretations are also explored. These findings provide new insights into the chemistry of thermogenic methane generation, and may provide an explanation of the elevated apparent temperatures recorded by the methane clumped-isotope thermometer in some natural gases. However, it remains unknown if the laboratory experiments capture the processes that occur at the longer time and lower temperatures of natural gas formation.

Seismic valve as the main mechanism for sedimentary fluid entrapment within extensional basin: example of the Lodève Permian Basin (Hérault, South of France).

NASA Astrophysics Data System (ADS)

Laurent, D.; Lopez, M.; Chauvet, A.; Imbert, P.; Sauvage, A. C.; Martine, B.; Thomas, M.

2014-12-01

During syn-sedimentary burial in basin, interstitial fluids initially trapped within the sedimentary pile are easily moving under overpressure gradient. Indeed, they have a significant role on deformation during basin evolution, particularly on fault reactivation. The Lodève Permian Basin (Hérault, France) is an exhumed half graben with exceptional outcrop conditions providing access to barite-sulfides mineralized systems and hydrocarbon trapped into rollover faults of the basin. Architectural studies shows a cyclic infilling of fault zone and associated S0-parallel veins according to three main fluid events during dextral/normal faulting. Contrasting fluid entrapment conditions are deduced from textural analysis, fluid inclusion microthermometry and sulfide isotope geothermometer: (i) the first stage is characterized by an implosion breccia cemented by silicifications and barite during abrupt pressure drop within fault zone; (ii) the second stage consists in succession of barite ribbons precipitated under overpressure fluctuations, derived from fault-valve action, with reactivation planes formed by sulphide-rich micro-shearing structures showing normal movement; and (iii) the third stage is associated to the formation of dextral strike-slip pull-apart infilling by large barite crystals and contemporary hydrocarbons under suprahydrostatic pressure values. Microthermometry, sulfide and strontium isotopic compositions of the barite-sulfides veins indicate that all stages were formed by mixing between deep basinal fluids at 230°C, derived from cinerite dewatering, and formation water from overlying sedimentary cover channelized trough fault planes. We conclude to a polyphase history of fluid trapping during Permian synrift formation of the basin: (i) a first event, associated with the dextral strike-slip motion on faults, leads to a first sealing of the fault zone; (ii) periodic reactivations of fault planes and bedding-controlled shearing form the main mineralized ore bodies by the single action of fluid overpressure fluctuations, undergoing changes in local stress distribution and (iii) a final tectonic activation of fault linked to last basinal fluid and hydrocarbon migration during which shear stress restoration on fault plane is faster than fluid pressure build-up.

The Thermal Waters of Jordan

NASA Astrophysics Data System (ADS)

Sass, I.; Schäffer, R.

2012-04-01

In a recent field campaign all known natural hot spring areas of Jordan were investigated. Their hydrochemical properties including some fundamental isotopes were measured. Jordan's thermal springs can be classified into four thermal provinces (Nahr Al-Urdun, Hammamat Ma'in, Zara and Wadi Araba province), with similar hydrochemical and geologicalsettings. Thermal springs of Hammamat Ma'in and Zara province are situated on prominent faults. Reservoir temperature estimation with the Mg-corrected Na-K-Ca geothermometer indicates temperatures between 61 °C and 82 °C. Even taking into account the increased geothermal gradient at Dead Sea's east coast, the water's origin has to be considered mainly in deeper formations. Carbon dioxide, emitted by tertiary basalts situated close to the springs, may be responsible for gas lift. Mineralisation and δ18O-values indicate, that the spring water's origin is mostly fossil, i.e. not part of the global water cycle. It is shown, that ground water mining led to a shift within δ18O-ratio during the last 30 years due to a reduction of shallow water portion in addition to a dislocation of the catchment area. Ground water mining will impact the thermal spring productivity and quality anyway in the future. Present-day precipitation rates and catchment areas in Dead Sea region are by far not sufficient to explain relative high discharge. For the Hammamat Ma'in Province is documented, that discharge and maximal spring water temperatures are constant during the last 50 years, showing marginal seasonal oscillation and negligible influence by short-term climatic changes. The water characteristics of Hammamat Ma'in and Zara province are related. However, Zara waters feature systematically less ion concentration and lower temperatures due to a stronger influence of vadose water. The springs of Nahr Al-Urdun province are recharged mainly by shallow groundwater. Thus temperature and mineralisation is lower than at the springs at the Dead Sea. Thermal waters of Wadi Araba province show the lowest mineralisation due to their origin of mostly sandstones. The main ion's proportion and δ18O-ratio indicate a mixture of fossil and vadose groundwater.

Hydrogeochemical exploration of geothermal prospects in the Tecuamburro Volcano region, Guatemala

USGS Publications Warehouse

Janik, C.J.; Goff, F.; Fahlquist, L.; Adams, A.I.; Alfredo, Roldan M.; Chipera, S.J.; Trujillo, P.E.; Counce, D.

1992-01-01

Chemical and isotopic analyses of thermal and nonthermal waters and of gases from springs and fumaroles are used to evaluate the geothermal potential of the Tecuamburro Volcano region, Guatemala. Chemically distinct geothermal surface manifestations generally occur in separate hydrogeologic areas within this 400 km2 region: low-pressure fumaroles with temperatures near local boiling occur at 1470 m elevation in a sulfur mine near the summit of Tecuamburro Volcano; non-boiling acid-sulfate hot springs and mud pots are restricted to the Laguna Ixpaco area, about 5 km NNW of the sulfur mine and 350-400 m lower in elevation; steam-heated and thermal-meteoric waters are found on the flanks of Tecuamburro Volcano and several kilometers to the north in the andesitic highland, where the Infernitos fumarole (97??C at 1180 m) is the primary feature; neutral-chloride hot springs discharge along Rio Los Esclavos, principally near Colmenares at 490 m elevation, about 8-10 km SE of Infernitos. Maximum geothermometer temperatures calculated from Colmenares neutral-chloride spring compositions are ???180??C, whereas maximum subsurface temperatures based on Laguna Ixpaco gas compositions are ???310??C. An exploration core hole drilled to a depth of 808 m about 0.3 km south of Laguna Ixpaco had a bottom-hole temperature of 238??C but did not produce sufficient fluids to confirm or chemically characterize a geothermal reservoir. Hydrogeochemical data combined with regional geologic interpretations indicate that there are probably two hydrothermal-convection systems, which are separated by a major NW-trending structural boundary, the Ixpaco fault. One system with reservoir temperatures near 300??C lies beneath Tecuamburro Volcano and consists of a large vapor zone that feeds steam to the Laguna Ixpaco area, with underlying hot water that flows laterally to feed a small group of warm, chloriderich springs SE of Tecuamburro Volcano. The other system is located beneath the Infernitos area in the andesitic highland and consists of a lower-temperature (150-190??C) reservoir with a large natural discharge that feeds the Colmenares hot springs. ?? 1992.

Mg-Fe Isotope Systems of Mantle Xenoliths: Constrains on the Evolution of Siberian Craton

NASA Astrophysics Data System (ADS)

An, Y.; Kiseeva, E. S.; Sobolev, N. V.; Zhang, Z.

2017-12-01

Mantle xenoliths bring to the surface a variety of lithologies (dunites, lherzolites, harzburgites, wehrlites, eclogites, pyroxenites, and websterites) and represent snapshots of the geochemical processes that occur deep within the Earth. Recent improvements in the precision of the MC-ICP-MS measurements have allowed us to expand the amount of data on Mg and Fe isotopes for mantle-derived samples. For instance, to constrain the isotopic composition of the Earth based on the study of spinel and garnet peridotites (An et al., 2017; Teng et al., 2010), to trace the origin and to investigate the isotopic fractionation mechanism during metamorphic process using cratonic or orogenic eclogites (Li et al., 2011; Wang et al., 2012) and to reveal the metasomatism-induced mantle heterogeneity by pyroxenites (Hu et al., 2016). Numerous multi-stage modification events and mantle layering are detected in the subcontinental lithospheric mantle under the Siberian craton (Ashchepkov et al., 2008a; Sobolev et al., 1975, etc). Combined analyses of Mg and Fe isotopic systems could provide new constraints on the formation and evolution of the ancient cratonic mantle. In order to better constrain the magnitude and mechanism of inter-mineral Mg and Fe isotopic fractionations at high temperatures, systematic studies of mantle xenoliths are needed. For example, theoretical calculations and natural samples measurements have shown that large equilibrium Mg isotope fractionations controlled by the difference in coordination number of Mg among minerals could exist (Huang et al., 2013; Li et al., 2011). Thus, the Mg isotope geothermometer could help us trace the evolution history of ancient cratons. In this study we present Mg and Fe isotopic data for whole rocks and separated minerals (clinopyroxene (cpx) and garnet (grt)) from different types of mantle xenoliths (garnet pyroxenites, eclogites, grospydites and garnet peridotites) from a number of kimberlite pipes in Siberian craton (Udachnaya, Obnazhennaya, Mir, and Zagadochnaya). The large Mg and Fe isotope fractionations between clinopyroxene and garnet for various mantle rocks (Δ26Mg cpx-gnt= 0.360‰ 0.888‰, Δ56Fe cpx-gnt= 0.018‰ 0.348‰) indicate that the Siberian cratonic lithosphetic mantle has undergone multiple complex metasomatic and re-equilibration events.

Evolution of the blueschist and greenschist facies rocks of Sifnos, Cyclades, Greece

NASA Astrophysics Data System (ADS)

Matthews, Alan; Schliestedt, Manfred

1984-11-01

The metamorphism on the island of Sifnos is characterized by the Eocene development of a coherent highpressure blueschist terrane and an early Miocene greenschist facies overprint. This study documents the metamorphic evolution of the blueschist assemblages, still preserved in the northern parts of the island, and their subsequent transformation into greenschists in the central and southern parts. The oxygen isotope geothermometry is based on calibrations for quartz, pyroxenes and magnetite (Matthews et al. 1983a) augmented by revised calibrations for the minerals muscovite ( Δ Qz-Mu=1.55×106 T -2), epidote ( δ Qz-Ep= 1.56+1.92 Δ ps)106 T -2), and rutile ( Δ Qz-Ru=4.54×106 T -2). Oxygen isotope analyses of minerals from the Blueschist unit of northern Sifnos give consistent fractionations which are independent of rock type. An average temperature of 455° C was obtained, although the scatter in temperatures deduced from the various geothermometers suggests that equilibration occurs under slightly changing physicochemical conditions. Analyses of minerals and whole rocks shows that pervasive equilibration in the presence of a common metamorphic fluid has not occurred. The minerals and whole rocks of the greenschists of central Sifnos are systematically enriched in 18O relative to the blueschist assemblages. Chemical data indicate that the greenschist overprint was accompanied by a metasomatic enrichment of Ca2+ and CO2. The petrologic, isotopic and chemical evidence favour a metamorphism governed by the infiltration of 18O-CO2 enriched aqueous solutions. It is reasonable to assume that this is connected with the Miocene magmatic activity observed throughout the Cyclades. The marbles separating the Blueschist from the Greenschist unit probably acted as barriers to fluid infiltration into the blueschists and were responsible for their preservation. The pressure of the blueschist metamorphism is estimated at 14±2 kbar, corresponding to a depth of ca. 50 km. The structural style and stratigraphy of Sifnos are suggestive of the subduction of a continental margin sequence. It is clear that the considerable tectonic depression may be associated with continental collision and underthrusting.

Hydrogen and oxygen stable isotope signatures of goethite hydration waters by thermogravimetry-enabled laser spectroscopy

DOE Office of Scientific and Technical Information (OSTI.GOV)

Oerter, Erik; Singleton, Michael; Davisson, Lee

The hydrogen and oxygen stable isotope composition (δ 2H and δ 18O values) of mineral hydration waters can give information on the environment of mineral formation. Here we present and validate an approach for the stable isotope analysis of mineral hydration waters based on coupling a thermogravimetric analyzer with a laser-based isotope ratio infrared spectroscopy instrument (Picarro L-2130i), which we abbreviate as TGA-IRIS. TGA-IRIS generates δ 2H and δ 18O values of liquid water samples with precision for δ 2H of ± 1.2‰, and for δ 18O of ± 0.17‰. For hydration waters in goethite, precision for δ 2H rangesmore » from ± 0.3‰ to 1.6‰, and for δ 18O ranges from ± 0.17‰ to 0.27‰. The ability of TGA-IRIS to generate detailed water yield data and δ 2H and δ 18O values of water at varying temperatures allows for the differentiation of water in varying states of binding on mineral surfaces and within the mineral matrix. TGA-IRIS analyses of hydrogen isotopes in goethite yields δ 2H values that reflect the hydrogen of the OH – phase in the mineral and are comparable to that made by IRMS and found in the literature. In contrast, δ 18O values on goethite reflect the oxygen in OH – groups bound to Fe (Fe-OH group), and not the oxygen bound only to Fe (Fe-O group) in the mineral crystal lattice, and may not be comparable to literature δ 18O values made by IRMS that reflect the total O in the mineral. TGA-IRIS presents the possibility to isotopically differentiate the various oxygen reservoirs in goethite, which may allow the mineral to be used as a single mineral geothermometer. As a result, TGA-IRIS measurements of hydration waters are likely to open new avenues and possibilities for research on hydrated minerals.« less

Hydrogen and oxygen stable isotope signatures of goethite hydration waters by thermogravimetry-enabled laser spectroscopy

DOE PAGES

Oerter, Erik; Singleton, Michael; Davisson, Lee

2017-10-22

The hydrogen and oxygen stable isotope composition (δ 2H and δ 18O values) of mineral hydration waters can give information on the environment of mineral formation. Here we present and validate an approach for the stable isotope analysis of mineral hydration waters based on coupling a thermogravimetric analyzer with a laser-based isotope ratio infrared spectroscopy instrument (Picarro L-2130i), which we abbreviate as TGA-IRIS. TGA-IRIS generates δ 2H and δ 18O values of liquid water samples with precision for δ 2H of ± 1.2‰, and for δ 18O of ± 0.17‰. For hydration waters in goethite, precision for δ 2H rangesmore » from ± 0.3‰ to 1.6‰, and for δ 18O ranges from ± 0.17‰ to 0.27‰. The ability of TGA-IRIS to generate detailed water yield data and δ 2H and δ 18O values of water at varying temperatures allows for the differentiation of water in varying states of binding on mineral surfaces and within the mineral matrix. TGA-IRIS analyses of hydrogen isotopes in goethite yields δ 2H values that reflect the hydrogen of the OH – phase in the mineral and are comparable to that made by IRMS and found in the literature. In contrast, δ 18O values on goethite reflect the oxygen in OH – groups bound to Fe (Fe-OH group), and not the oxygen bound only to Fe (Fe-O group) in the mineral crystal lattice, and may not be comparable to literature δ 18O values made by IRMS that reflect the total O in the mineral. TGA-IRIS presents the possibility to isotopically differentiate the various oxygen reservoirs in goethite, which may allow the mineral to be used as a single mineral geothermometer. As a result, TGA-IRIS measurements of hydration waters are likely to open new avenues and possibilities for research on hydrated minerals.« less

Comparative geothermometry of recent Hawaiian eruptions

NASA Astrophysics Data System (ADS)

Helz, Rosalind Tuthill; Banks, Norman G.; Heliker, Christina; Neal, Christina A.; Wolfe, Edward W.

1995-09-01

In this paper we compare lava temperatures measured using Cr-Al thermocouples or infrared spectrometry with estimated quenching temperatures based on the glass geothermometry calibration of Helz and Thornber (1987). Comparative data are available for the April 1982 and September 1982 summit eruptions, the Pu'u O'o east rift eruption (1983-1986), all three eruptions at Kilauea, and the 1984 Mauna Loa eruption. The results show that quenching temperatures, based on the MgO contents of Kilauean glasses (TMgO), lie within ±10°C of field measurements using the infrared spectrometer for 85% of the samples. Where a Cr-Al thermocouple was used, 90% of the field measurements lie within +1° to -11°C of TMgO for samples with Tfield > 1130°C. Samples where Tfield < 1130°C show larger divergence. The uncertainty in TMgO by itself is ±10°C, so the level of agreement between field measurements and TMgO is very good for Kilauean lavas. Systematic comparison of field measurements of temperature with glass geothermometry for the 1984 Mauna Loa eruption suggests that, although the field and glass temperatures lie within ±10°C of each other, the Kilauean TMgO calibration is nevertheless not appropriate for Mauna Loa glasses and that actual quenching temperatures for Mauna Loa samples will lie 10°-20°C higher than would be predicted from the Kilauea calibration curve. Consideration of possible effects of variable volatile content suggest that in most cases these are small. Samples erupted early in an eruption may reflect preeruptive water contents different enough to affect TMgO significantly, but later spatter samples and all flow samples appear to have equilibrated at low enough water contents for the calibration to be applicable. We conclude that the MgO-based geothermometer can be applied to glassy Kilauean samples to give temperatures that generally will lie within ±10°C of a field measurement. Plots of glass MgO content versus time, if a suitable sample base is available, should give a thorough, quantitative record of the thermal history of any Kilauean eruption.

The Blacktail Creek Tuff: an analytical and experimental study of rhyolites from the Heise volcanic field, Yellowstone hotspot system

NASA Astrophysics Data System (ADS)

Bolte, Torsten; Holtz, Francois; Almeev, Renat; Nash, Barbara

2015-02-01

The magma storage conditions of the 6.62 Ma Blacktail Creek Tuff eruption, belonging to the Heise volcanic field (6.62-4.45 Ma old) of the Yellowstone hotspot system, have been investigated by combining thermobarometric and experimental approaches. The results from different geothermometers (e.g., Fe-Ti oxides, feldspar pairs, apatite and zircon solubility, and Ti in quartz) indicate a pre-eruptive temperature in the range 825-875 °C. The temperature estimated using two-pyroxene pairs varies in a range of 810-950 °C, but the pyroxenes are probably not in equilibrium with each other, and the analytical results of melt inclusion in pyroxenes indicate a complex history for clinopyroxene, which hosts two compositionally different inclusion types. One natural Blacktail Creek Tuff rock sample has been used to determine experimentally the equilibrium phase assemblages in the pressure range 100-500 MPa and a water activity range 0.1-1.0. The experiments have been performed at fluid-present conditions, with a fluid phase composed of H2O and CO2, as well as at fluid-absent conditions. The stability of the quartzo-feldspathic phases is similar in both types of experiments, but the presence of mafic minerals such as biotite and clinopyroxene is strongly dependent on the experimental approach. Possible explanations are given for this discrepancy which may have strong impacts on the choice of appropriate experimental approaches for the determination of magma storage conditions. The comparison of the composition of natural phases and of experimentally synthesized phases confirms magma storage temperatures of 845-875 °C. Melt water contents of 1.5-2.5 wt% H2O are required to reproduce the natural Blacktail Creek Tuff mineral assemblage at these temperatures. Using the Ti-in-quartz barometer and the Qz-Ab-Or proportions of natural matrix glasses, coexisting with quartz, plagioclase and sanidine, the depth of magma storage is estimated to be in a pressure range between 130 and 250 MPa.

Hydrogeochemistry and environmental impact of geothermal waters from Yangyi of Tibet, China

NASA Astrophysics Data System (ADS)

Guo, Qinghai; Wang, Yanxin; Liu, Wei

2009-02-01

The Yangyi geothermal field, located 72 km northwest to Lhasa City, capital of Tibet, has a high reservoir temperature up to at least 207.2 °C. The geothermal waters from both geothermal wells and hot springs belong to the HCO 3 (+CO 3)-Na type. Factor analysis of all the chemical constituents shows that they can be divided into two factors: F 1 factor receives the contributions of SO 42-, Cl -, SiO 2, As, B, Na +, K +, and Li +; whereas F 2 factor is explained by HCO 3-, F -, CO 32-, Ca 2+, and Sr 2+. The F 1 factor can be regarded as an indicator of the reservoir temperature distribution at Yangyi, but its variable correlation with the results of different geothermometers (Na-K, quartz and K-Mg) does not allow one to draw further inferences. Different from F 1, the F 2 factor is an indicator of a group of hydrogeochemical processes resulting from the CO 2 pressure decrease in geothermal water during its ascent from the deep underground, including transformation of HCO 3- to CO 32-, precipitation of Ca 2+ and Sr 2+, and release of F - from some fluoride-bearing minerals of reservoir rocks. The plot of enthalpy vs. chloride, prepared on the basis of Na-K equilibrium temperatures, suggests that a parent geothermal liquid (PGL) with Cl - concentration of 185 mg/L (that of sample YYT-8) and enthalpy of 1020 J/g (corresponding to a temperature of 236-237 °C, i.e., somewhat higher than that of sample YYT-6) is present in the geothermal reservoir of the Yangyi area, below both the Qialagai valley and the Bujiemu valley, although the samples less affected by mixing and cooling (YYT-6 and YYT-7) come from the second site. The discharge of geothermal waters with high contents of toxic elements such as B, As and F into the Luolang River, the only drinking water source for local residents, has caused slight pollution of the river water. Great care should therefore be taken in the geothermal water resource management at Yangyi.

Volatile emissions and gas geochemistry of Hot Spring Basin, Yellowstone National Park, USA

USGS Publications Warehouse

Werner, C.; Hurwitz, S.; Evans, William C.; Lowenstern, J. B.; Bergfeld, D.; Heasler, H.; Jaworowski, C.; Hunt, A.

2008-01-01

We characterize and quantify volatile emissions at Hot Spring Basin (HSB), a large acid-sulfate region that lies just outside the northeastern edge of the 640??ka Yellowstone Caldera. Relative to other thermal areas in Yellowstone, HSB gases are rich in He and H2, and mildly enriched in CH4 and H2S. Gas compositions are consistent with boiling directly off a deep geothermal liquid at depth as it migrates toward the surface. This fluid, and the gases evolved from it, carries geochemical signatures of magmatic volatiles and water-rock reactions with multiple crustal sources, including limestones or quartz-rich sediments with low K/U (or 40*Ar/4*He). Variations in gas chemistry across the region reflect reservoir heterogeneity and variable degrees of boiling. Gas-geothermometer temperatures approach 300????C and suggest that the reservoir feeding HSB is one of the hottest at Yellowstone. Diffuse CO2 flux in the western basin of HSB, as measured by accumulation-chamber methods, is similar in magnitude to other acid-sulfate areas of Yellowstone and is well correlated to shallow soil temperatures. The extrapolation of diffuse CO2 fluxes across all the thermal/altered area suggests that 410 ?? 140??t d- 1 CO2 are emitted at HSB (vent emissions not included). Diffuse fluxes of H2S were measured in Yellowstone for the first time and likely exceed 2.4??t d- 1 at HSB. Comparing estimates of the total estimated diffuse H2S emission to the amount of sulfur as SO42- in streams indicates ~ 50% of the original H2S in the gas emission is lost into shallow groundwater, precipitated as native sulfur, or vented through fumaroles. We estimate the heat output of HSB as ~ 140-370??MW using CO2 as a tracer for steam condensate, but not including the contribution from fumaroles and hydrothermal vents. Overall, the diffuse heat and volatile fluxes of HSB are as great as some active volcanoes, but they are a small fraction (1-3% for CO2, 2-8% for heat) of that estimated for the entire Yellowstone system.

Magma chamber cooling by episodic volatile expulsion as constrained by mineral vein distributions in the Butte, Montana Cu-Mo porphyry deposit

NASA Astrophysics Data System (ADS)

Daly, K.; Karlstrom, L.; Reed, M. H.

2016-12-01

The role of hydrothermal systems in the thermal evolution of magma chambers is poorly constrained yet likely significant. We analyze trends in mineral composition, vein thickness and overall volumetric fluid flux of the Butte, Montana porphyry Cu-Mo deposit to constrain the role of episodic volatile discharge in the crystallization of the source magma chamber ( 300 km3of silicic magma). An aqueous fluid sourced from injection of porphyritic dikes formed the Butte porphyry Cu network of veins. At least three separate pulses of fluid through the system are defined by alteration envelopes of [1] gray sericite (GS); [2] early-dark micaceous (EDM), pale-green sericite (PGS), and dark-green sericite (DGS); and [3] quartz-molybdenite (Qmb) and barren-quartz. Previous research using geothermometers and geobarometers has found that vein mineral composition, inferred temperatures and inferred pressures vary systematically with depth. Later fluid pulses are characterized by lower temperatures, consistent with progressive cooling of the source. We have digitized previously unused structural data from Butte area drill cores, and applied thermomechanical modeling of fluid release from the source magma chamber through time. Vein number density and vein thickness increase with depth as a clear function of mineralogy and thus primary temperature and pressure. We identify structural trends in the three fluid pulses which seem to imply time evolution of average vein characteristics. Pulses of Qmb-barren quartz and EDM-PGS-DGS (1st and 2nd in time) exhibit increasing vein number density (157 & 95 veins/50m, respectively) and thickness (300mm & 120mm, respectively) as a function of depth. EDM-PGS-DGS has a shallower peak in vein density (800m) than Qmb-barren quartz (>1600m). These data provide the basis for idealized mechanical models of hydrofractures, to predict driving pressures and to compare with existing source temperatures and total fluid volumes in order to estimate the total enthalpy of each fluid pulse. We then compare with models for conductive cooling and crystallization of the source magma chamber to estimate the importance of hydrothermal fluid expulsion in the total heat budget. Such models should also provide constraints on the timing and ultimately the origin of pulsed volatile release at Butte.

Crystal zoning in a large-volume ignimbrite: constraints on the thermal history of a supervolcano magma system

NASA Astrophysics Data System (ADS)

Matthews, N. E.; Pyle, D. M.; Wilson, C. J.

2009-12-01

Chemical zoning of crystals provides an important archive of information that allows for the reconstruction of complex thermal histories and changes in melt composition of the magma reservoir during crystallization. Here we investigate cathodoluminescence (CL) and Ti zonation in quartz crystals extracted from pumices from the Whakamaru and Rangitaiki ignimbrite units (part of the large-volume Whakamaru Group Ignimbrites), New Zealand, to reconstruct the thermal history of the parent magma chamber(s). CL intensity images are taken as a proxy for Ti content and temperature variation during crystal growth, and direct estimates of temperature are made using the TitaniQ geothermometer (Wark & Watson 2006 Cont. Min. Pet.) based on Ti concentration in quartz. These results are reviewed in comparison with temperatures from Fe-Ti oxide geothermometry. Quartz zoning is also compared to zonation in feldspars (using BSE imaging) from the same pumice clasts in order to establish the degree to which different crystal species record similar or contrasting magmatic histories. Quartz crystals in Whakamaru pumice display a variety of CL zoning patterns and resorption boundaries. Overgrowths typically appear to truncate CL growth zoning within the crystal core, indicating periods of resorption and subsequent re-growth - consistent with magma recharge causing a marked change in conditions (temperature and/or volatile saturation) and multi-stage crystallisation. Crystals typically display a dark (lower Ti) resorbed core, with an abrupt change to a CL-bright rim, although irregular textures and complex variations between crystals are observed. Core-to-rim profiles of Ti concentration in analysed quartz crystals show Ti variations within the range 50-225 ppm, corresponding to crystallisation temperatures of 733-935°C (assuming TiO2 activity in the melt of 0.6), with the lowest values recorded in the crystal core, increasing in a step-wise pattern towards the rim. These values are consistent with Fe-Ti oxide temperature data for the same pumice clasts which provide a temperature range of 660-933°C. It is inferred that the major steps in Ti content (and thus CL brightness) represent short-term temperature fluctuations due to magma chamber recharge and rejuvenation of a crystal mush, while rim temperatures are likely to record the magma temperature at the time of eruption.

Precursory signals preceding by a few months a major Vrancea earthquake: their possible role in devising a risk-preparedness strategy

NASA Astrophysics Data System (ADS)

Anghelache, M. A.; Chitea, F.; Marin, C.; Tudorache, A.; Mitrofan, H.

2010-05-01

Early warning systems for earthquakes, based on the P wave's arrival at the surface, are very useful in reducing the industrial facilities vulnerability - specifically by turning off gas and electrical power supplies. Early warning systems may also save human lives, if the population was formerly subject to a coherent program of education and training. However, as far as economic losses or social disruption are concerned, this type of very short-term warning systems remains poorly efficient. The present paper investigates what pre-event actions could be efficiently taken, provided that some longer in advance information was gained about the possibility of an extreme event occurrence in a particular area. In Vrancea seismic region (Romania), where 2-3 catastrophic (M≥7) earthquakes are known to occur each century, there is currently investigated the possibility of taking advantage of the hydrochemical precursory signals detected at some specific saline springs, which proved to be of deep-origin and to be suitable for chemical geothermometry diagnoses. Such anomalous Na-K-Mg geothermometer signatures have been continuously recorded for more than one year, prior to a significant (M=6) Vrancea seismic event. There seemed, in particular, that the concerned experimental data-points approached the transition between the pre- and post-earthquake regimes progressively, over a period of a few months. This circumstance could prove to be outstandingly favorable for launching - within a reasonable time-window before the anticipated large earthquake - appropriate sets of protection actions. The considered protection actions include mainly checking and improving the reaction-systems, with special emphasis on the reaction ability of the medical systems and verifying the infrastructure systems, especially in order to prevent critical contingencies like bottle-necks. A full collaboration between the earthquake-response professionals and the building occupants is necessary in order to develop a response plan addressing emergency protection methods (e.g.: shoring the valuable moveable heritage objects, propping equipment and materials which are liable to overturn etc). Security measures should also imply the training in counter theft, arson or any other criminal activity. Acknowledgements: The research was performed with financial support from the CNMP within 31036/ 2007 and 31024/2007 scientific projects.

Estimation and application of the thermodynamic properties of aqueous phenanthrene and isomers of methylphenanthrene at high temperature

NASA Astrophysics Data System (ADS)

Dick, Jeffrey M.; Evans, Katy A.; Holman, Alex I.; Jaraula, Caroline M. B.; Grice, Kliti

2013-12-01

Estimates of standard molal Gibbs energy (ΔGf°) and enthalpy (ΔHf°) of formation, entropy (S°), heat capacity (CP°) and volume (V°) at 25 °C and 1 bar of aqueous phenanthrene (P) and 1-, 2-, 3-, 4- and 9-methylphenanthrene (1-MP, 2-MP, 3-MP, 4-MP, 9-MP) were made by combining reported standard-state properties of the crystalline compounds, solubilities and enthalpies of phenanthrene and 1-MP, and relative Gibbs energies, enthalpies and entropies of aqueous MP isomers from published quantum chemical simulations. The calculated properties are consistent with greater stabilities of the β isomers (2-MP and 3-MP) relative to the α isomers (1-MP and 9-MP) at 25 °C. However, the metastable equilibrium values of the abundance ratios 2-MP/1-MP (MPR) and (2-MP + 3-MP)/(1-MP + 9-MP) (MPI-3) decrease with temperature, becoming <1 at ∼375-455 °C. The thermodynamic model is consistent with observations of reversals of these organic maturity parameters at high temperature in hydrothermal and metamorphic settings. Application of the model to data reported for the Paleoproterozoic Here’s Your Chance (HYC) Pb-Zn-Ag ore deposit (McArthur River, Northern Territory, Australia) indicates a likely effect of high-temperature equilibration on reported values of MPR and MPI-3, but this finding is contingent on the location within the deposit. If metastable equilibrium holds, a third aromatic maturity ratio, 1.5 × (2-MP + 3-MP)/(P + 1-MP + 9-MP) (MPI-1), can be used as a proxy for oxidation potential. Values of logaH2aq determined from data reported for HYC and for a sequence of deeply buried source rocks are indicative of more reducing conditions at a given temperature than those inferred from data reported for two sets of samples exposed to contact or regional metamorphism. These results are limiting-case scenarios for the modeled systems that do not account for effects of non-ideal mixing or kinetics, or external sources or transport of the organic matter. Nevertheless, quantifying the temperature dependence of equilibrium constants of organic reactions enables the utilization of organic maturity parameters as relative geothermometers at temperatures higher than the nominal limits of the oil window.

Fluid Geochemistry of the Capelinhos Vent Site. A Key to Understand the Lucky Strike Hydrothermal Vent Field (37°N, MAR).

NASA Astrophysics Data System (ADS)

Leleu, T.; Chavagnac, V.; Cannat, M.; Ceuleneer, G.; Castillo, A.; Menjot, L.

2015-12-01

The Lucky Strike hydrothermal field is situated at the mid-Atlantic ridge, south of the Azores, on top of a central volcano within the axial valley. The volcano is composed of a fossil lava lake surrounded by three volcanic cones. An Axial Magma Chamber (AMC) is reported 3.4km below the seafloor. The active venting sites are situated around the fossil lava lake and are directly linked to the heat supplied by the AMC. High temperature fluids from the Lucky Strike field were sampled in 2013, 2014 and 2015 in order to document the depth of the reaction zone, subsurface mixing, geographical control and magmatic degassing. A new active site named Capelinhos was discovered approximately 1.5km eastward from the lava lake, during exploration by ROV Victor6000 - MoMARsat cruise, 2013. It is composed of 10m-high chimneys discharging black smoker-type fluid. Fluid temperatures were 328°C in 2013 and decreased to 318°C in 2014 and 2015. Capelinhos fluids are Cl-depleted by 55% compared to seawater indicating phase separation at depth. In comparison, the other sites range from 6% enrichment (2608/Y3 site) to 22% depletion (Eiffel tower site). Si geothermobarometry of Y3 site estimates quartz equilibration at P=300 bars and T=360-380°C, coherent with Fe/Mn geothermometer (T=370±10°C). For Capelinhos, Fe/Mn suggests 398°C (±10°C) which is close to the critical point of seawater (P=300 bars and T=407°C). Other geothermobarometer uses Si/Cl vapor-like fluid to constrain depth of the top of reaction zone and predicts significant bias due to mixing along the up-flow zone. Application gives P=~370 bars, T=~435°C at Capelinhos and P=~390 bars, T=~440°C at Eiffel tower. This is further sustained by end-member 87Sr/86Sr=0.7038, which indicates little interaction of Capelinhos vent fluids with seawater-derived fluid, compared to other vapor-like sites with 87Sr/86Sr=0.7043. Because of its external location, Capelinhos site isn't influenced by the complex tectonic context of the lava lake.

Estimation of the geothermal potential of the Caldara di Manziana site in the Mts Sabatini Volcanic District (Central Italy) by integrating geochemical data and 3D-GIS modelling.

NASA Astrophysics Data System (ADS)

Ranaldi, Massimo; Lelli, Matteo; Tarchini, Luca; Carapezza, Maria Luisa; Patera, Antonio

2016-04-01

High-enthalpy geothermal fields of Central Italy are hosted in deeply fractured carbonate reservoirs occurring in thermally anomalous and seismically active zones. However, the Mts. Sabatini volcanic district, located north of Rome, has an interesting deep temperatures (T), but it is characterized by low to very low seismicity and permeability in the reservoir rocks (mostly because of hydrothermal self-sealing processes). Low PCO2 facilitates the complete sealing of the reservoir fractures, preventing hot fluids rising and, determining a low CO2 flux at the surface. Conversely, high CO2 flux generally reflects a high pressure of CO2, suggesting that an active geothermal reservoir is present at depth. In Mts. Sabatini district, the Caldara of Manziana (CM) is the only zone characterized by a very high CO2 flux (188 tons/day) from a surface of 0.15 km2) considering both the diffuse and viscous CO2 emission. This suggests the likely presence of an actively degassing geothermal reservoir at depth. Emitted gas is dominated by CO2 (>97 vol.%). Triangular irregular networks (TINs) have been used to represent the morphology of the bottom of the surficial volcanic deposits, the thickness of the impervious formation and the top of the geothermal reservoir. The TINs, integrated by T-gradient and deep well data, allowed to estimate the depth and the temperature of the top of the geothermal reservoir, respectively to ~-1000 m from the surface and to ~130°C. These estimations are fairly in agreement with those obtained by gas chemistry (818

Volatile behaviour and magmatic processes leading to the 1257 climatic eruption of Samalas (Indonesia)

NASA Astrophysics Data System (ADS)

Vidal, C. M.; Metrich, N.; Komorowski, J. C.; Pratomo, I.; Kartadinata, N.; Lavigne, F.

2017-12-01

The 1257 caldera-forming eruption of Samalas was one of most powerful eruptions of the Holocene (VEI 7). It blasted in the stratosphere tephra and gases which stand as the largest emissions of the Common Era. The sulphuric acid veil engendered a severe decrease of temperatures in the Northern hemisphere during 3 years, favouring crop failures and enhancing deadly famines across Europe in the mid-13th century. Petrological and mineralogical study of the Holocene products of the Rinjani-Samalas complex and their melt inclusions showed that the medieval eruption evacuated 40 km3 of chemically homogeneous trachydacite (64.0±0.4 wt% SiO2; 8.1±0.1 wt% Na2O+K2O, normalized on anhydrous basis). Its mineral paragenesis consists of plagioclase with patchy zoned calcic cores (An82-75) surrounded by sodic bands (An50-43), in association with amphibole (magnesio-hastingsite), orthopyroxene (Mg# 0.66-0.73), titano-magnetite, iron sulphide and apatite. Rare extremely calcic plagioclase (An91-92) records the early stage of crystallization. The trachydacitic magma derived from its parent high alumina basalt (HAB) through 80% of fractional crystallisation in the lower crust involving the peritectic formation of (cryptic) amphibole. Trachydacitic batches of magma were further extracted and transferred to shallow depth (3-4 km). The range of water contents and temperatures measured in melt inclusions (989±10°C 3.7±0.3 wt% H2O) and discrepancies with geothermometers (895-980°C) show that the magma batches crystallized in-situ but isolated under conditions of water-saturation. Volatile concentrations in melt inclusions, minerals, matrix glasses and whole-rocks of the Rinjani-Samalas suite show that prior to the 1257 eruption, volatiles were distributed between the trachydacitic melt, the exsolved C-H-O-S vapour phase, polymetallic sulphides, amphibole and apatite. A total of 158 Tg SO2, 227 Tg Cl and up to 1.3 Tg Br were released during the eruption. The good agreement with sulphur proxies derived from ice core records confirms that the pre-eruptive vapour phase contributed to 80% of the S yield, and suggests that the plume dynamics enhanced the stratospheric injection of climate-impacting gases.

Temporal Evolution of Volcanic and Plutonic Magmas Related to Porphyry Copper Ores Based on Zircon Geochemistry

NASA Astrophysics Data System (ADS)

Dilles, J. H.; Lee, R. G.; Wooden, J. L.; Koleszar, A. M.

2015-12-01

Porphyry Cu (Mo-Au) and epithermal Au-Ag ores are globally associated with shallow hydrous, strongly oxidized, and sulfur-rich arc intrusions. In many localities, long-lived magmatism includes evolution from early andesitic volcanic (v) and plutonic (p) rocks to later dacitic or rhyolitic compositions dominated by plutons. We compare zircon compositions from three igneous suites with different time spans: Yerington, USA (1 m.y., p>v), El Salvador, Chile (4 m.y., p>v), and Yanacocha, Peru (6 m.y., v>p). At Yerington granite dikes and ores formed in one event, at ES in 2 to 3 events spanning 3 m.y., and at Yanacocha in 6 events spanning 5 m.y. At both ES and Yanacocha, high-Al amphiboles likely crystallized at high temperature in the mid-crust and attest to deep magmas that periodically recharged the shallow chambers. At Yanacocha, these amphiboles contain anhydrite inclusions that require magmas were sulfur-rich and strongly oxidized (~NNO+2). The Ti-in-zircon geothermometer provides estimates of 920º to 620º C for zircon crystallization, and records both core to rim cooling and locally high temperature rim overgrowths. Ore-related silicic porphyries yield near-solidus crystallization temperatures of 750-650°C consistent with low zircon saturation temperatures. The latter zircons have large positive Ce/Ce* and small negative Eu/Eu*≥0.4 anomalies attesting to strongly oxidized conditions (Ballard et al., 2001), which we propose result from crystallization and SO2 loss to the magmatic-hydrothermal ore fluid (Dilles et al., 2015). The Hf, REE, Y, U, and Th contents of zircons are diverse in the magma suites, and Th/U vs Yb/Gd plots suggest a dominant role of crystal fractionation with lesser roles for both crustal contamination and mixing with high temperature deep-sourced mafic magma. Ce/Sm vs Yb/Gd plots suggest that magma REE contents at <900°C are dominated by early crystallization of hornblende and apatite, and late crystallization (~<780°C) of titanite. Magma mixing and crustal contamination are most evident in pre-ore magmas, whereas ore-forming intrusions at low temperatures are dominated by crystal fractionation. Thus, zircon provides evidence for cyclic crystallization and mafic recharge that enrich late silicic melts in incompatible ore components water, sulfur, chlorine and metals.

Geochemical assessment of hydrocarbon migration phenomena: Case studies from the south-western margin of the Dead Sea Basin

NASA Astrophysics Data System (ADS)

Sokol, Ella; Kozmenko, Olga; Smirnov, Sergey; Sokol, Ivan; Novikova, Sofya; Tomilenko, Anatoliy; Kokh, Svetlana; Ryazanova, Tatyana; Reutsky, Vadim; Bul'bak, Taras; Vapnik, Yevgeny; Deyak, Michail

2014-10-01

Calcite veins with fluid and solid bitumen inclusions have been discovered in the south-western shoulder of the Dead Sea rift within the Masada-Zohar block, where hydrocarbons exist in small commercial gas fields and non-commercial fields of heavy and light oils. The gas-liquid inclusions in calcite are dominated either by methane or CO2, and aqueous inclusions sometimes bear minor dissolved hydrocarbons. The enclosed flake-like solid bitumen matter is a residue of degraded oil, which may be interpreted as “dead carbon”. About 2/3 of this matter is soot-like amorphous carbon and 1/3 consists of n-C8sbnd C18 carboxylic acids and traces of n-alkanes, light dicarboxylic acids, and higher molecular weight (>C20) branched and/or cyclic carboxylic acids. Both bitumen and the host calcites show genetic relationship with mature Maastrichtian chalky source rocks (MCSRs) evident in isotopic compositions (δ13C, δ34S, and δ18O) and in REE + Y patterns. The bitumen precursor may have been heavy sulfur-rich oil which was generated during the burial compaction of the MCSR strata within the subsided blocks of the Dead Sea graben. The δ18O and δ13C values and REE + Y signatures in calcites indicate mixing of deep buried fluids equilibrated with post-mature sediments and meteoric waters. The temperatures of fluid generation according to Mg-Li-geothermometer data range from 55 °С to 90 °С corresponding to the 2.5-4.0 km depths, and largely overlap with the oil window range (60-90 °С) in the Dead Sea rift (Hunt, 1996; Gvirtzman and Stanislavsky, 2000; Buryakovsky et al., 2005). The bitumen-rich vein calcites originated in the course of Late Cenozoic rifting and related deformation, when tectonic stress triggers damaged small hydrocarbon reservoirs in the area, produced pathways, and caused hydrocarbon-bearing fluids to rise to the subsurface; the fluids filled open fractures and crystallized to calcite with entrapped bitumen. The reported results are in good agreement with the existing views of maturation, migration, and accumulation of hydrocarbons, as well as basin fluid transport processes in the Dead Sea area.

The role of hydrothermal processes in the granite-hosted Zr, Y, REE deposit at Strange Lake, Quebec/Labrador: Evidence from fluid inclusions

NASA Astrophysics Data System (ADS)

Salvi, Stefano; Williams-Jones, Anthony E.

1990-09-01

The Strange Lake Zr, Y, REE, Nb, and Be deposit is hosted by a small, high-level, Late-Proterozoic peralkaline granite stock that intruded into high-grade metamorphic gneisses on the Quebec-Labrador border. The stock is extensively altered. Early alteration is manifested by the replacement of arfvedsonite with aegirine. Later alteration involved Ca-Na exchange. Zr, Ti, Y, REEs, Nb, and Be are concentrated in Ca-bearing minerals that, together with quartz, commonly pseudomorph Na-bearing minerals. Fluid inclusions in pseudomorphs comprise several distinct types: high-salinity (13 to 24 wt% NaCl eq.), Ca-rich aqueous inclusions that homogenize to liquid between 135 and 195°C; mixed aqueousmethane inclusions; methane inclusions; and solid-bearing inclusions. Aqueous-methane inclusions represent heterogeneous entrapment of immiscible high-salinity aqueous liquid and methane. Bastnäsite (tentatively identified by SEM analysis) occurs as a daughter mineral. Other daughter or trapped minerals include a Y, HREE-bearing mineral, possibly gagarinite, and hematite, galena, sphalerite, fluorite, pyrochlore, kutnahorite (?), and griceite (?). The first three inclusion types also occur in quartz in pegmatites and veins together with lower-temperature, lower-salinity, Na-dominated aqueous inclusions. The entrapment temperature inferred for the aqueous inclusions from microthermometry and the Na-K-Ca geothermometer range from 155 to 195°C for the higher-salinity inclusions and 100 to 165°C for the low-salinity inclusions. A model is proposed in which the intrusion of a peralkaline granite to high crustal levels initiated a ground/formational water-dominated hydrothermal system in adjacent gabbroic, calc-silicate, and graphitic gneisses. Reaction of the high-salinity, Ca-rich liquid with the graphitic gneisses led to the production of an immiscible methane gas. Subsequent interaction of this liquid with the granite led to extensive replacement of sodic minerals by calcium analogues at temperatures of less than 200°C. Some time after the onset of Ca metasomatism the high-salinity liquid mixed with a Ca-poor, low-salinity, low-temperature liquid that had leached F and rare metals from the granite. Yttrium and REE mineral deposition occurred as a result of the decreased ligand concentration that accompanied fluorite deposition during mixing of the Ca-rich and Ca-poor aqueous liquids.

Fluid geochemistry of a deep-seated geothermal resource in the Puna plateau (Jujuy Province, Argentina)

NASA Astrophysics Data System (ADS)

Peralta Arnold, Y.; Cabassi, J.; Tassi, F.; Caffe, P. J.; Vaselli, O.

2017-05-01

This study focused on the geochemical and isotopic features of thermal fluids discharged from five zones located in the high altitude Puna plateau (Jujuy Province between S 22°20‧-23°20‧ and W 66°-67°), i.e. Granada, Vilama, Pairique, Coranzulí and Olaroz. Partially mature waters with a Na+-Cl- composition were recognized in all the investigated zones, suggesting that a deep hydrothermal reservoir hosted within the Paleozoic crystalline basement represents the main hydrothermal fluid source. The hydrothermal reservoirs are mainly recharged by meteoric water, although based on the δ18O-H2O and δD-H2O values, some contribution of andesitic water cannot be completely ruled out. Regional S-oriented faulting systems, which generated a horst and graben tectonics, and NE-, NW- and WE-oriented transverse structures, likely act as preferentially uprising pathways for the deep-originated fluids, as also supported by the Rc/Ra values (up to 1.39) indicating the occurrence of significant amounts of mantle He (up to 16%). Carbon dioxide, the most abundant compound in the gas phase associated with the thermal waters, mostly originated from a crustal source, although the occurrence of CO2 from a mantle source, contaminated by organic-rich material due to the subduction process, is also possible. Relatively small and cold Na+-HCO3--type aquifers were produced by the interaction between meteoric water and Cretaceous, Palaeogene to Miocene sediments. Dissolution of evaporitic surficial deposits strongly affected the chemistry of the thermal springs in the peripheral zones of the study area. Geothermometry in the Na-K-Ca-Mg system suggested equilibrium temperatures up to 200 °C for the deep aquifer, whereas lower temperatures (from 105 to 155 °C) were inferred by applying the H2 geothermometer, likely due to re-equilibrium processes during the thermal fluid uprising within relatively shallow Na-HCO3 aquifers. The great depth of the geothermal resource (possibly > 5000 m b.g.l.) is likely preventing further studies aimed to evaluate possible exploitation, although the occurrence of Li- and Ba-rich deposits associated may attract financial investments, giving a pulse for the development of this remote region.

Intensive Variables in Primary Kimberlite Magmas (Lac de Gras, N.W.T., Canada) and Application for Diamond Preservation

NASA Astrophysics Data System (ADS)

Fedortchouk, Y.; Canil, D.; Carlson, J. A.

2002-12-01

Crystallization temperatures (T) and oxygen fugacity (fO2) are not well constrained for kimberlites. Knowledge of these intensive variables of kimberlite melt is important for understanding the origin and evolution of kimberlites and prediction of diamond preservation in the magma. Difficulties in interpreting the equilibrium mineral assemblages in kimberlites and the high degree of secondary alteration usually complicate use of mineral geothermometers and oxygen barometers. Some of Lac de Gras (N.W.T., Canada) kimberlites are extremely fresh and provide opportunity to apply mineral thermobarometers. The presence of numerous chromite inclusions in the rims of olivine phenocrysts allows application of the olivine-spinel thermometer and oxygen barometer to constrain T and fO2 of the melt. We performed T and fO2 calculations on samples from three kimberlite pipes - the Leslie, Aaron and Grizzly. The T obtained from olivine - chromite pairs for crystallization of olivine phenocryst rims are 1050° to 1100°C +/- 50°C (calculated at 1 GPa). Few olivine - chromite pairs from Leslie and Grizzly record higher temperatures of 1250° - 1350°C. The cores of olivine phenocrysts usually lack chromite inclusions and their crystallization T and fO2 could not be estimated. The fO2 recorded by coexisting olivine and chromite are +0.3 to 1.0 +/- 0.4 log units more oxidized than the nickel-nickel oxide (NNO) buffer. The established fO2 of kimberlites would require fO2 in their mantle source to be higher than that of cratonic mantle and oceanic lithosphere producing MORB's but comparable to the source of subduction-related magmas. The T and fO2 for the Lac de Gras kimberlites constrain the path of any mantle material entrained in these magmas in fO2-T-P space and provide limits on diamond destructive processes. Diamonds are not stable in kimberlite magma and are oxidized to CO2 or converted into graphite. The former process is more favorable for their preservation. The results of out thermo-barometric calculations show that at any pressure the Lac de Gras kimberlites were above the Graphite (Diamond)-CCO buffer. Diamonds entrained in these kimberlites were moved into stability field of CO2 without graphitization, favoring better preservation of diamonds.

Spectroscopy `outside the box': Towards wider application of NMR to minerals and glasses with abundant paramagnetic cations - Fe, Ni, Co, and Cu silicates

NASA Astrophysics Data System (ADS)

Stebbins, J. F.

2017-12-01

Since the early applications of solid-state NMR (Nuclear Magnetic Resonance) to silicates in the early 1980's, this powerful method has been widely applied to problems of short- to medium-range structure, particularly for materials in which order/disorder is critical, such as crystalline solid solutions, glasses, and even melts. However, almost all such work has been on materials with low (< a few %) contents of ions with unpaired electron spins. Such spins interact strongly with NMR-observed nuclear spins, and can cause severe line broadening and loss of information, in some cases making spectra nearly unobservable. Many groups of minerals with abundant, paramagnetic transition metals (notably Fe2+) and rare earth cations, as well as wide, petrologically important ranges of glass composition have thus been excluded. Inspired by in-depth NMR studies of 31P, 7Li, and other nuclides in lithium-transition metal oxide and phosphate battery materials (C. Grey and others), and with some serendipitous discovery plus persistence to look far outside of "normal" parameter space, we have recently shown that high resolution, structurally informative spectra can actually be obtained for silicate, oxide, and phosphate solid solutions with moderate (0.1 up to 10%) contents of paramagnetic cations such as Fe2+, Ni2+, Co2+ and REE3+. Very recently we have extended this to observe some of the first quantitative NMR spectra of silicate minerals in which a paramagnetic transition metal is the major cation, obtaining useful data for a series of Cu2+ silicates, fayalite (Fe2SiO4) and Ni- and Co- equivalents of diopside (CaMSi2O6). New data for glasses of the latter compositions may be the first such accurate results for any transition metal-rich glass. Although we are still far from a detailed theoretical understanding of these data, the spectra for the glasses are quite different from those of the crystals, suggesting the possibility of medium-range ordering and clustering of NiO and CoO-rich regions. If this conclusion holds up, it may have major implications for thermodynamic models of activities of such components in melts, which in turn are important for a number of geothermometers and barometers based on mineral-melt partitioning.

Crystallization Temperatures of Lower Crustal Gabbros from the Oman Ophiolite and the Persistence of the 'Mush Zone' at Intermediate/Fast Spreading Ridges

NASA Astrophysics Data System (ADS)

VanTongeren, J. A.

2017-12-01

Oceanic crust is formed when mantle-derived magmas are emplaced at the ridge axis, a zone of intense rifting and extension. Magmas begin to cool and crystallize on-axis, forming what is termed the "Mush Zone", a region of partially molten rocks. Several attempts have been made to understand the nature of the Mush Zone at fast spreading mid-ocean ridges, specifically how much partial melt exists and how far off-axis the Mush Zone extends. Geophysical estimates of P-wave velocity perturbations at the East Pacific Rise show a region of low velocity approximately 1.5-2.5 km off-axis, which can be interpreted to be the result of higher temperature [e.g. Dunn et al., 2000, JGR] or the existence of partial melt. New petrological and geochemical data and methods allow for the calculation of the lateral extent of the Mush Zone in the lower oceanic crust on exposed sections collected from the Oman ophiolite, a paleo-fast/intermediate spreading center. I will present new data quantifying the crystallization temperatures of gabbros from the Wadi Khafifah section of lower oceanic gabbros from the Oman ophiolite. Crystallization temperatures are calculated with the newly developed plagioclase-pyroxene REE thermometer of Sun and Liang [2017, Contrib. Min. Pet.]. There does not appear to be any systematic change in the crystallization temperature of lower crustal gabbros with depth in the crust. In order to quantify the duration of crystallization and the lateral extent of the Mush Zone of the lower crust, crystallization temperatures are paired with estimates of the solidus temperature and cooling rate determined from the same sample, previously constrained by the Ca diffusion in olivine geothermometer/ geospeedometer [e.g. VanTongeren et al., 2008 EPSL]. There is no systematic variation in the closure temperature of Ca in olivine, or the cooling rate to the 800°C isotherm. These results show that gabbros throughout the lower crust of the Oman ophiolite remain in a partially molten state for an average of 10,000 years. Assuming a paleo-spreading rate similar to that of the East Pacific Rise, this translates to a "Mush Zone" of partially molten rock up to 1 km off-axis, slightly less than the low velocity zone observed geophysically on the East Pacific Rise.

Equilibrium and non-equilibrium controls on the abundances of clumped isotopologues of methane during thermogenic formation in laboratory experiments: Implications for the chemistry of pyrolysis and the origins of natural gases

USGS Publications Warehouse

Shuai, Yanhua; Douglas, Peter M.J.; Zhang, Shuichang; Stolper, Daniel A.; Ellis, Geoffrey S.; Lawson, Michael; Lewan, Michael; Formolo, Michael; Mi, Jingkui; He, Kun; Hu, Guoyi; Eiler, John M.

2018-01-01

Multiply isotopically substituted molecules (‘clumped’ isotopologues) can be used as geothermometers because their proportions at isotopic equilibrium relative to a random distribution of isotopes amongst all isotopologues are functions of temperature. This has allowed measurements of clumped-isotope abundances to be used to constrain formation temperatures of several natural materials. However, kinetic processes during generation, modification, or transport of natural materials can also affect their clumped-isotope compositions. Herein, we show that methane generated experimentally by closed-system hydrous pyrolysis of shale or nonhydrous pyrolysis of coal yields clumped-isotope compositions consistent with an equilibrium distribution of isotopologues under some experimental conditions (temperature–time conditions corresponding to ‘low,’ ‘mature,’ and ‘over-mature’ stages of catagenesis), but can have non-equilibrium (i.e., kinetically controlled) distributions under other experimental conditions (‘high’ to ‘over-mature’ stages), particularly for pyrolysis of coal. Non-equilibrium compositions, when present, lead the measured proportions of clumped species to be lower than expected for equilibrium at the experimental temperature, and in some cases to be lower than a random distribution of isotopes (i.e., negative Δ18 values). We propose that the consistency with equilibrium for methane formed by relatively low temperature pyrolysis reflects local reversibility of isotope exchange reactions involving a reactant or transition state species during demethylation of one or more components of kerogen. Non-equilibrium clumped-isotope compositions occur under conditions where ‘secondary’ cracking of retained oil in shale or wet gas hydrocarbons (C2-5, especially ethane) in coal is prominent. We suggest these non-equilibrium isotopic compositions are the result of the expression of kinetic isotope effects during the irreversible generation of methane from an alkyl precursor. Other interpretations are also explored. These findings provide new insights into the chemistry of thermogenic methane generation, and may provide an explanation of the elevated apparent temperatures recorded by the methane clumped-isotope thermometer in some natural gases. However, it remains unknown if the laboratory experiments capture the processes that occur at the longer time and lower temperatures of natural gas formation.

Geochemistry of thermal fluids in NW Honduras: New perspectives for exploitation of geothermal areas in the southern Sula graben

NASA Astrophysics Data System (ADS)

Capaccioni, Bruno; Franco, Tassi; Alberto, Renzulli; Orlando, Vaselli; Marco, Menichetti; Salvatore, Inguaggiato

2014-06-01

The results of a geochemical survey on thermal waters and, for the first time for this site, gas discharges in five geothermal sites (Azacualpa "La Cueva", Río Ulua, Río Gualcarque, El Olivar and Laguna de Agua Caliente) in NW Honduras are here presented and discussed. El Olivar and Laguna de Agua Caliente, in the southern part of the Sula graben are very close to a Quaternary basaltic field, whereas Azacualpa "La Cueva", Río Ulua and Río Gualcarque, located to the southwest of the Yojoa Lake, direcly emerge from the Cretaceous limestone deposits. The measured temperatures range between 37.5 and 104.8 °C. "Mature", alkaline, Na-SO4 thermal waters discharge from Azacualpa "La Cueva", while those from El Olivar and Laguna de Agua Caliente are "immature" and show a Na-HCO3 composition. Chemical equilibria of waters and gases from the Azacualpa "La Cueva" thermal springs indicate temperatures ranging from 150 to 200 °C. Conversely, gas discharges from El Olivar and Laguna de Agua Caliente have attained a partial chemical equilibrium in the liquid phase at slightly higher temperatures (200-250 °C), although gas-gas faster reactions involving CO seem to be adjusted in an isothermally separated vapor phase. Unlike Azacualpa, SiO2 geothermometer at El Olivar and Laguna de Agua Caliente indicates equilibrium temperatures for the liquid phase much lower than those calculated for the gas phase (≤ 120 °C). We conclude that thermal waters from the Azacualpa area likely represent the direct emergence of a water dominated reservoir having temperatures ≤ 150-200 °C. By contrast, at El Olivar and Laguna de Agua Caliente hot springs are supplied by a boiling shallow aquifer fed by a vapor phase rising from a steam-dominated zone. The above geochemical model is consistent with a geothermal reservoir hosted within the Cretaceous carbonate sequences of the Yojoa Group in the whole investigated sites. The reservoir extensively crops out in the Azacualpa area whereas the geothermal sites of the southern Sula graben (Laguna de Agua Caliente and El Olivar) are covered by the Oligocene-Miocene volcano-sedimentary sequences of the Matagalpa formation, possibly acting as efficient impermeable cap rocks. These results significantly differ from those reported by previous studies and emphasize that the southern Sula graben, in particular the El Olivar area, can represent among the investigated thermal springs, the most promising site for the exploitation of a high-enthalpy geothermal field.

Choice of 17O Abundance Correction Affects Δ47 and Thus Calibrations for Paleothermometry

NASA Astrophysics Data System (ADS)

Kelson, J.; Schauer, A. J.; Huntington, K. W.; Saenger, C.; Lechler, A. R.

2016-12-01

The clumped isotope composition of CO2 derived from carbonate (Δ47) varies with temperature, making it a valuable geothermometer with broad applications. However, its accuracy is limited by inter-laboratory discrepancies of carbonate reference materials and disagreement among Δ47-temperature calibrations. Here we use a suite of CO2-H2O equilibrations at known temperatures with a wide range in 13C and 18O compositions to show how the correction for the abundance of 17O impacts Δ47 and potentially explains these discrepancies. When a traditional value of 0.5164 is used for the fractionation between 17O and 18O (λ), corrected Δ47 in 23 °C CO2-H2O equilibrations exhibits a dependence on 13C composition that is equivalent to 20 ºC (Δ47 range of 0.06 ‰). In contrast, these discrepancies are effectively removed when λ=0.528, as in global meteoric waters. Furthermore, carbonate standards with identical formation temperatures have significantly different Δ47 when corrected using λ=0.5164, but agree within error when λ=0.528. The choice of λ affects the accuracy of all sample Δ47 values, unless the sample CO2, mass spectrometer reference gas, and equilibrated gases share the same 13C composition. The sensitivity of Δ47 to the choice of λ, and the apparent dependence on 13C when 0.5164 is used, are relevant to the abiogenic experiments used in Δ47-temperature calibrations given that precipitation methods involving CO2 bubbling produce carbonates depleted in 13C by tens of permil relative to methods that mix salts. We evaluate the influence of 17O correction on Δ47-temperature calibrations using a suite of 58 abiogenic carbonates precipitated at 4-85 ºC using CO2 bubbling and the mixing of salts. Aliquots of precipitated carbonates were digested at 25 and 90ºC, but all other preparatory and analytical variables were held constant. When corrected using λ=0.5164, various precipitation methods yield sub-parallel Δ47-temperature relationships with slopes of 0.034-0.044 (x 106/T2), but offset intercepts. Conversely, Δ47-temperature relationships overlap within error when λ=0.528. This suggests that the method used to correct for 17O abundance likely contributes to observed calibration discrepancies and that adopting λ=0.528 may reduce the uncertainty in Δ47 temperature reconstructions.

Morphological ripening of fluid inclusions and coupled zone-refining in quartz crystals revealed by cathodoluminescence imaging: Implications for CL-petrography, fluid inclusion analysis and trace-element geothermometry

NASA Astrophysics Data System (ADS)

Lambrecht, Glenn; Diamond, Larryn William

2014-09-01

Cathodoluminescence (CL) studies have previously shown that some secondary fluid inclusions in luminescent quartz are surrounded by dark, non-luminescent patches, resulting from fracture-sealing by late, trace-element-poor quartz. This finding has led to the tacit generalization that all dark CL patches indicate influx of low temperature, late-stage fluids. In this study we have examined natural and synthetic hydrothermal quartz crystals using CL imaging supplemented by in-situ elemental analysis. The results lead us to propose that all natural, liquid-water-bearing inclusions in quartz, whether trapped on former crystal growth surfaces (i.e., of primary origin) or in healed fractures (i.e., of pseudosecondary or secondary origin), are surrounded by three-dimensional, non-luminescent patches. Cross-cutting relations show that the patches form after entrapment of the fluid inclusions and therefore they are not diagnostic of the timing of fluid entrapment. Instead, the dark patches reveal the mechanism by which fluid inclusions spontaneously approach morphological equilibrium and purify their host quartz over geological time. Fluid inclusions that contain solvent water perpetually dissolve and reprecipitate their walls, gradually adopting low-energy euhedral and equant shapes. Defects in the host quartz constitute solubility gradients that drive physical migration of the inclusions over distances of tens of μm (commonly) up to several mm (rarely). Inclusions thus sequester from their walls any trace elements (e.g., Li, Al, Na, Ti) present in excess of equilibrium concentrations, thereby chemically purifying their host crystals in a process analogous to industrial zone refining. Non-luminescent patches of quartz are left in their wake. Fluid inclusions that contain no liquid water as solvent (e.g., inclusions of low-density H2O vapor or other non-aqueous volatiles) do not undergo this process and therefore do not migrate, do not modify their shapes with time, and are not associated with dark-CL zone-refined patches. This new understanding has implications for the interpretation of solids within fluid inclusions (e.g., Ti- and Al-minerals) and for the elemental analysis of hydrothermal and metamorphic quartz and its fluid inclusions by microbeam methods such as LA-ICPMS and SIMS. As Ti is a common trace element in quartz, its sequestration by fluid inclusions and its depletion in zone-refined patches impacts on applications of the Ti-in-quartz geothermometer.

Trace element composition and cathodoluminescence of kyanite and its petrogenetic implications

NASA Astrophysics Data System (ADS)

Müller, Axel; van den Kerkhof, Alfons M.; Selbekk, Rune S.; Broekmans, Maarten A. T. M.

2016-09-01

Kyanite crystals from fourteen localities worldwide were analysed for their abundances of the trace elements Na, Mg, K, Ca, Ti, V, Cr, Mn, and Fe and cathodoluminescence (CL) properties. Based on protolith type, metamorphic setting, and distinctive trace element fingerprints, a genetic classification of kyanite-bearing rocks is suggested: (A) Al-rich metasediments which commonly contain coarse-grained quartz-kyanite segregations; (B) metamorphosed granitic rocks, specifically granulites; (C) metamorphosed argillic alteration zones hosted originally in felsic igneous rocks; (D) metamorphosed argillic alteration zones hosted originally in mafic igneous rocks; and (E) metamorphosed mafic to ultramafic rocks, specifically eclogites. Vanadium and Cr concentrations reflect both protolith and host rock compositions and therefore may provide a geochemical fingerprint for the nature of the protolith. The incorporation of Fe into kyanite is largely controlled by oxygen fugacity during kyanite formation, and therefore, in most cases, its concentration cannot be related to that of the protolith. From our results, Ti concentration appears to be related to metamorphic grade, particularly formation temperature. If proven by further studies, Ti-in-kyanite may provide a useful geothermometer. Correlation of trace element abundances with CL spectra confirms that common red CL, which is composed of the spectral bands centred at 1.69 eV (734 nm), 1.75 eV (708 nm), and 1.80 eV (689 nm), is related to Cr3+ defects. CL spectra of most kyanites show in addition a low-intensity blue emission centred at 2.56 eV (485 nm). Correlation of the intensity of the blue emission with Ti suggests that it is related to or sensitized by Ti4+ or Ti3+ defects. Kyanites with >3200 µgg-1 Fe show generally no detectable CL due to the CL-quenching effect of Fe2+. Our findings provide new criteria in the exploration for and quality assessment of new kyanite deposits. The Ti content, one of the critical contaminants of kyanite products, besides Fe, Ca, and Mg, appears predictable from the observed correlation of Ti with formation temperature. Iron will be hard to predict because its incorporation is mainly controlled by the oxidizing conditions during kyanite formation and the estimation of these conditions requires advanced analytical methods. Magnesium and Ca are consistently low in all investigated samples. From a regional exploration viewpoint, group C and D kyanites have the lowest Ti and relative low Fe and, therefore, will be most refractory. Due to their attractive blue colour, kyanite-bearing rocks of group C have potential as ornamental or dimension stone.

Potential Temperatures of Sources of MORB, OIB and LIPs Based on AL Partitioning Between Olivine and Spinel

NASA Astrophysics Data System (ADS)

Sobolev, A. V.; Batanova, V. G.; Krasheninnikov, S.; Borisov, A.; Arndt, N.; Kuzmin, D.; Krivolutskaya, N.; Sushevskaya, N.

2013-12-01

Knowledge of potential temperatures of convecting mantle is required for the understanding the global processes on the Earth [1]. The common way to estimate these is the reconstruction of primary melt compositions and liquidus temperatures based on the Fe-Mg partitioning between olivine and melt. This approach requires knowledge of the compositions of primitive melts in equilibrium with olivine alone as well as composition of olivine equilibrium with primary melts. This information is in most cases unavailable or of questionable quality. Here we report a new approach to obtain crystallization temperatures of primary melts based on the olivine-spinel Al-Cr geothermometer [2]. The advantages of this approach are: (1) low rate of diffusion of Al in the olivine, which promises to preserve high magmatic temperatures and (2) common presence of spinel in assemblage with high-Mg olivine. In order to decipher influence of elevated Ti concentrations in spinel we have run several experiments at high temperatures (1400-1200 degree C), atmospheric pressure and controled oxygen fugacity. We also analysed over two thousand spinel inclusions and high-Mg host olivines from different MORB, OIB, LIP and Archean komatiites on the JXA-8230 EPMA at ISTerre, Grenoble, France. Concentrations of Al, Ti, Na, P, Zn, Cr, Mn, Ca, Co, Ni were determined with a precision of 10 ppm (2 standard errors) using a newly developed protocol [3]. When available, we also analysed matrix glass and glass inclusions in olivine and found that temperature estimations from olivine-spinel (Al-Cr) and olivine-melt (Fe-Mg) [4] equilibrium match within (+/-30 degree C). The results show contrasting crystallization temperatures of Mg-rich olivine of the same Fo content from different types of mantle-derived magmas, from the lowest (down to 1220 degree C) for MORB to the highest (up to 1550 degree C) for komatiites and Siberian meimechites. These results match predictions from Fe-Mg olivine-melt equilibrium and confirm the relatively low temperature of the convecting mantle source of MORB and higher temperatures in the mantle plumes that produce the OIB of Iceland, Hawaii, Gorgona, Archean komatiites and several LIPs (e.g. Siberian, Decan). [1] McKenzie & Bickle, 1988, J. Petr. 29, p 625-679. [2] Wan et al, 2008, Am. Min. 93, p1142-1147. [3] Batanova & Sobolev, 2013, Min. Mag.,p 667, DOI :10.1180/minmag2013.077.5.2 [4] Ford et al, 1983, J. Petr. 24, p 256-265.

The origin and geochemical characteristics of rutile in eluvial and fluvial-alluvial placers and quartz veins of the Menderes Massif from the Neoproterozoic Pan-African Belt, Western Turkey

NASA Astrophysics Data System (ADS)

Kuşcu, Mustafa; Cengiz, Oya; Işık, Kayhan; Gül, E. Kübra

2018-07-01

Rutile occur in important amounts within Quaternary detrital sediments, and quartz veins which cut down the Paleozoic aged Eşme formation in the Menderes Massif on the Neoproterozoic Pan-Afrikan Belt in the west of Turkey. As a result of erosion, transport and accumulation of rutile-bearing quartz veins in the mica schists of the Eşme formation outcropped between Eşme (Uşak) and Kula (Manisa), the placer rutile occurrences occur in terraces, fluvial-alluvial and eluvial deposits. This study investigates the element content of rutile, oxygen isotope ratios of rutile and quartz, and formation temperature of rutile related to titanium source rock. Field observations show that rutiles are located in quartz veins that cut the schists. After these veins were fragmented and eroded, blocks of quartz with rutile and rutile grains are transported into clastic sediments in slope debris (eluvial), terraces and recent fluvial-alluvial deposits. Whereas quartz, rutile, ilmenite, and albite are found in the paragenesis of the rutile-bearing quartz vein fragments, the placers forming the terraces and current fluvial-alluvial deposits contain quartz, albite, muscovite, orthoclase, kaolinite, rutile, dravite, ilmenite, and zircon. The rutile grains in the examined placers and quartz vein fragments have grain sizes ranging from mm fractions to 5-6 cm. The major oxide compositions of the rutile grains have average values of 94 wt.% TiO2, 1.5 wt.% Fe2O3, 0.5 wt.% SiO2, and 0.3 wt.% Al2O3. The rutile samples have average values Nb of 1424 ppm, V of 980 ppm, W of 192 ppm, Ta of 94 ppm, and Zr of 73 ppm. The rutiles in the study area are defined as iron-rich rutile "nigrine" due to high iron content. Quartz veins are host rocks of rutile grains in the terrace and fluvial-aluvial sediments. The rutile-bearing quartz veins may be sourced from the Lower-Middle Miocene aged granites which are intruded the rocks in the Menderes Massif. Based on the analysis results of the methods of Zr thermometer from Zr values containing rutile and quartz-rutile geothermometer from oxygen isotope results (13.5‰ and 6‰) of quartz and rutile samples, the formation temperature of the rutile-bearing quartz veins were found to be at temperatures of 537 °C and 561 °C, respectively. These temperatures indicate that the rutile-bearing quartz veins may be in a temperature range between pegmatitic and/or hydrothermal stages.

Two type of ultarabasic melts - alkaline picrite and meimechite. Was there a united general magma?

NASA Astrophysics Data System (ADS)

Asavin, A. M.

2009-04-01

The most interesting ultrabasic volcanic lavas in Maimecha Kotuj alkaline province province (South Taimur peninsula) are alkaline picrites and meimechites. These volcanites are extremely enriched in MgO (up to 32wt%) and consist of olivine phenocrysts and dark fine-grain groundmass, sometimes having similar nature of the komatiite spinifex-texture. Many authors believed that all series of ultrabasic lavas were formed from one primitive melt by fractionation of olivine crystals, or adding Ol xenocrysts into the liquid. This view supported the model of the one-stage large grade melting of the mantle. We can test the hypotheses by our materials (composition of the series meimechites and picrites groundmass and olivine and chromite phenocrysts). Points composition of groundmass and rock connected demonstrate the fractionation from picritic and meimechitic melts olivine. The main difference consist from the CaO, Al2O3 MgO ratio. And alkaline contents Na2O and K2O. We offer for explain this difference the mechanism of mixing primary meimechite liquids with carbonatic fluid-melt component. These special alkaline melt can bring CaO, Na2O, K2O, TiO2 in deep mantle regions and mixing with meimechites melts from the local picrite's generation region. These trends break down into two different fields in the plane Ln-Ab-Fo from the Ln-Fo-Ne-Q system. We would assume that the fields lie on different sides of the thermal barrier. The boundary may be regarded as Di-Ab cotectic projection on the plane Fo-Ak-Ab. We drew to the same conclusion when building the least-square calculation model of the relation between meimechite and picrite. This scheme is supported by overflow of the temperature of Ol equilibrium in the picritic and meimechitic melts. Temperature was determined by several Ol/Liq geothermometers (Ariskin, Leeman, Toplis et other researchers using Ol- melt equilibrium reaction) by the Mg, Fe, Ca, Mn and Cr content. It follows from these results that the one-stage model of mantle melting is not valid in this case. We can assume simultaneous and parallel process of mantle melting with the resulting formation of a set of picrite and meimechites dykes. The additional evidence of the chief role of the meimechite melt is the great field of the meimechites lavas and tuffs which exposed on the left board of the Maimecha rever. The picrites lavas practically is absent.

MIRA: A new approach to measuring Δ $47 in carbonates and geothermometry of MVT type deposits

NASA Astrophysics Data System (ADS)

Dennis, P. F.; Vinen, S. J.

2009-04-01

Clumped isotope thermometry is based on the thermodynamics of the order-disorder reaction for 18O and 13C: 13C16O16O16O + 12C18O16O16O = 13C18O16O16O + 12C16O16O16O At high temperatures 18O is randomly distributed between 12C and 13C in the carbonate anion. However, at lower temperatures there is a tendency for the 18O to cluster together with 13C. At low temperatures (T < 150oC) the degree of ordering, as measured by 47 of the CO2 that is produced by reaction of the carbonate with phosphoric acid ((13C18O16Osample/13C18O16Ostochastic)-1) is a potentially useful geothermometer (Eiler, 2007). However, for reliable temperature estimates to better than +/- 1oC at near earth surface temperatures requires measurement of 1000*47 to better than +/-0.005. Given that the 47 isotopologue occurs at a natural abundance of just 40ppm in CO2 this is a challenging measurement for stable isotope ratio mass spectrometry. We have developed a new instrument MIRA to accurately measure such small isotope ratios. MIRA is configured with a 50cm dispersion analyser, dual inlet, a high sensitivity Nier type source, 6 faraday collectors at m/z = 44, 45, 46, 47, 48 and 49 and ultra stable and linear detection and integration electronics. Using a dual inlet measurement precisions for 1000*47 are better than +/-0.01. To date isotopic clusters have just been used to estimate near surface and diagenetic temperatures to 75oC. We are using MIRA and the clumped isotope thermometer to assess formation temperatures (up to 150oC) and the timing of MVT Pb/Zn mineralisation in the Pennines, UK orefield. Because temperature estimates are based on an internal order-disorder reaction, they are independent of the isotopic composition of the formation waters making it possible independently to track changes in the ^18O composition of mineralising fluids. With sufficient resolution (+/- 2 - 5oC) we aim to map temperature distributions in order to better constrain the hydrothermal system. This is the first application of clumped isotopes to 'elevated' temperature thermometry. Eiler, J.M., 2007, 'Clumped-isotope' geochemistry - The study of naturally occurring multiply substituted isotopologues. Earth and Planetary Science Letters, 262, 309-327

Thermobarometry of mafic igneous rocks based on clinopyroxene-liquid equilibria, 0 30 kbar

NASA Astrophysics Data System (ADS)

Putirka, K.; Johnson, Marie; Kinzler, Rosamond; Longhi, John; Walker, David

1996-02-01

Models for estimating the pressure and temperature of igneous rocks from co-existing clino-pyroxene and liquid compositions are calibrated from existing data and from new data obtained from experiments performed on several mafic bulk compositions (from 8 30 kbar and 1100 1475° C). The resulting geothermobarometers involve thermodynamic expressions that relate temperature and pressure to equilibrium constants. Specifically, the jadeite (Jd; NaAlSi2O6) diopside/hedenbergite (DiHd; Ca(Mg, Fe) Si2O6) exchange equilibrium between clinopyroxene and liquid is temperature sensitive. When compositional corrections are made to the calibrated equilibrium constant the resulting geothermometer is (i) 104 T=6.73-0.26* ln [Jdpx*Caliq*FmliqDiHdpx*Naliq*Alliq] -0.86* ln [MgliqMgliq+Feliq]+0.52*ln [Caliq] an expression which estimates temperature to ±27 K. Compared to (i), the equilibrium constant for jadeite formation is more sensitive to pressure resulting in a thermobarometer (ii) P=-54.3+299* T104+36.4* T104 ln [Jdpx[Siliq]2*Naliq*Alliq] +367*[Naliq*Alliq] which estimates pressure to ± 1.4 kbar. Pressure is in kbar, T is in Kelvin. Quantities such as Naliq represent the cation fraction of the given oxide (NaO0.5) in the liquid and Fm=MgO+FeO. The mole fractions of Jd and diopside+hedenbergite (DiHd) components are calculated from a normative scheme which assigns the lesser of Na or octahedral Al to form Jd; any excess AlVI forms Calcium Tschermak’s component (CaTs; CaAlAlSiO6); Ca remaining after forming CaTs and CaTiAl2O6 is taken as DiHd. Experimental data not included in the regressions were used to test models (i) and (ii). Error on predictions of T using model (i) is ±40 K. A pressure-dependent form of (i) reduces this error to ±30 K. Using model (ii) to predict pressures, the error on mean values of 10 isobaric data sets (0 25 kbar, 118 data) is ±0.3 kbar. Calculating thermodynamic properties from regression coefficients in (ii) gives VJd f of 23.4 ±1.3 cm3/mol, close to the value anticipated from bar molar volume data (23.5 cm3/mol). Applied to clinopyroxene phenocrysts from Mauna Kea, Hawaii lavas, the expressions estimate equilibration depths as great as 40 km. This result indicates that transport was sufficiently rapid that at least some phenocrysts had insufficient time to re-equilibrate at lower pressures.

Oceanic crust within the paleozoic Granjeno Schist, northeastern Mexico. Remnants of the Rheic and paleo-Pacific Ocean.

NASA Astrophysics Data System (ADS)

Torres Sanchez, Sonia Alejandra; Augustsson, Carita; Rafael Barboza Gudiño, Jose; Jenchen, Uwe; Torres Sanchez, Dario; Aleman Gallardo, Eduardo; Abratis, Michael

2015-04-01

Late Paleozoic metamorphic rocks in Mexico are related to the Laurentia-Gondwana collision in Carboniferous time, during Pangaea amalgamation. Vestiges of the Mexican Paleozoic continental configuration are present in the Granjeno Schist, the metamorphic basement of the Sierra Madre Oriental. Field work and petrographic analysis reveal that the Granjeno Schist comprises metamorphic rocks with both sedimentary (psammite, pelite, turbidite, conglomerate, black shale) and igneous (tuff, lava flows, pillow lava and ultramafic bodies) protoliths. The chlorite geothermometer and the presence of phengite in the metasedimentary units as well as 40Ar/39Ar ages on metavolcanic and metaultramafic rocks indicate that the Granjeno Schist was metamorphosed under sub-greenschist to greenschist facies with temperatures ranging from 250-345°C with 2.5 kbar during Carboniferous time (330±30 Ma). The presence of metabasalt, metacumulate, serpentinite and talc bodies suggests an oceanic tectonic setting for the evolution of the Granjeno Schist. Serpetinite rocks have mesh, granular and ribbon textures which indicate recrystallization and metasomatic events. The serpentinite rocks are enriched in the very large incompatible elements Cs, U, and Zr and depleted in Ba, Sr, Pb, Zr and Ce. Normalized REE patterns (LaN/YbN = 0.51 - 19.95 and LaN/SmN = 0.72 - 9.08) of the serpentinite and talc/soapstone are characteristic of peridotite from both suprasubduction and mid-ocean ridge zones. Serpentinite from the Granjeno Schist have spinel content which can reveal different stages of evolution in host serpentinite. The composition of chromite indicates that they belong to podiform chromite that may have crystallized from mid-ocean ridge magma. Al-chromite in the serpentinite is characterized by #Cr 0.48 to 0.55, which indicates a depleted mantle source affected by 17 to 18% of partial melting. The ferritchromite has #Cr values of 0.93 to 1.00 which indicates a metamorphic origin. Our study suggests at least two serpentinization stages. The first serpentinization stage is related to an ocean-floor environment. At this stage, mesh-textured serpentinite formed under static conditions under subgreenschist to greenschist conditions. The second serpentinization stage occurred under greenschist to low amphibole conditions. During this stage Cr-spinel progressively was replaced by ferritchromite with magnetite rims due to regional metamorphism. Tectonic contact of the serpentinite with metavolcanic and metasedimentary rocks indicates lithospheric mantle slivers juxtaposed during the metamorphism of the Granjeno Schist during Pennsylvanian time. This metamorphic event occurred in an active continental margin. It represents the last events of the southern closure of the Rheic Ocean and Permo-Carboniferous convergence of Pacific plates on the western margin of Pangea.

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

DOE Office of Scientific and Technical Information (OSTI.GOV)

Ghanashayam Neupane; Earl D. Mattson; Travis L. McLing

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 nestedmore » 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 explicitly accounts for boiling, mixing, and CO2 degassing. RTEst modeling results indicate that the well water samples are mixed with up to 75% of the near surface groundwater. Relatively, Ca-(Mg)-HCO3 type water samples are more diluted than the Na-HCO3 type water samples. However, both water types result in similar reservoir temperatures, up to 150 °C. Samples in the vicinity of faults produced higher reservoir temperatures than samples away from the faults. Although both the silica-enthalpy mixing and RTEst models indicated promising geothermal reservoir temperatures, evaluation of the subsurface permeability and extent of the thermal anomaly is needed to define the hydrothermal potential of the Newdale geothermal resource.« less

Geochemical studies of abyssal lavas recovered by DSRV Alvin from Eastern Galapagos Rift, Inca Transform, and Ecuador Rift: 2. Phase chemistry and crystallization history

NASA Astrophysics Data System (ADS)

Perfit, Michael R.; Fornari, Daniel J.

1983-12-01

A diverse suite of lavas recovered by DSRV Alvin from the eastern Galapagos rift and Inca transform includes mid-ocean ridge tholeiitic basalts (MORB), iron- and titanium-enriched basalts (FeTi basalts), and abyssal andesites. Rock types transitional in character (ferrobasalts and basaltic andesites) were also recovered. The most mafic glassy basalts contain plagioclase, augite, and olivine as near-liquidus phases, whereas in more fractionated basalts, pigeonite replaces olivine and iron-titanium oxides crystallize. Plagioclase crystallizes after pyroxenes and iron-titanium oxides in andesites, possibly due to increased water contents or cooling rates. Apatite phenocrysts are present in some andesitic glasses. Ovoid sulfide globules are also common in many lavas. Compositional variations of phenocrysts in glassy lavas reflect changes in magma chemistry, temperature of crystallization, and cooling rate. The overall chemical variations parallel the chemical evolution of the lava suite and are similar to those in other fractionated tholeiitic complexes. Elemental partitioning between plagioclase-, pyroxene-, and olivine-glass pairs suggests that equilibration occurred at low pressure in a rather restricted temperature range. Various geothermometers indicate that the most primitive MORB began to crystallize between 1150° and 1200°C with fo2 < 10-7 atm. Coexisting iron-titanium oxides in more evolved lavas yield temperatures ˜1025°C to as low as 910°C withfo2 from 10-8 to 10-12 atm. PH 2 o could have been as high as 1 kbar during andesite crystallization. Compositions of the lavas from the Galapagos rift follow the experimentally determined (1 atm-QFM) liquid line of descent. Least squares calculations for the major elements indicate that the entire suite of lavas can be produced by fractional crystallization of successive residual liquids from a MORB parent magma. FeTi basalts represent 30-65 cumulative weight percent crystallization of plagioclase, augite, and olivine. An additional 30-50% fractionation of pyroxenes, plagioclase, titanomagnetite, and possible apatite is required to generate andesite from FeTi basalt liquids. The presence of partially resorbed mafic xenocrysts in some andesites, FeTi basalt inclusions in these xenocrysts, high-silica glass inclusions in basaltic andesites, and the transitional chemistry of basaltic andesites are evidence that some magma mixing occurred during crystal fractionation. The diversity of lava types recovered at single dive sites suggests that low-pressure fractional crystallization is a very efficient process beneath the eastern Galapagos rift and that isolated magma bodies must be present at shallow levels beneath the accretionary locus. Voluminous FeTi basalts erupted at the rift-transform intersection are genetically related to the rift lavas, but their restricted chemistry reflects different thermal and tectonic controls on their petrogenesis.

Igneous phenocrystic origin of K-feldspar megacrysts in granitic rocks from the Sierra Nevada batholith

USGS Publications Warehouse

Moore, J.G.; Sisson, T.W.

2008-01-01

Study of four K-feldspar megacrystic granitic plutons and related dikes in the Sierra Nevada composite batholith indicates that the megacrysts are phenocrysts that grew in contact with granitic melt. Growth to megacrystic sizes was due to repeated replenishment of the magma bodies by fresh granitic melt that maintained temperatures above the solidus for extended time periods and that provided components necessary for K-feldspar growth. These intrusions cooled 89-83 Ma, are the youngest in the range, and represent the culminating magmatic phase of the Sierra Nevada batholith. They are the granodiorite of Topaz Lake, the Cathedral Peak Granodiorite, the Mono Creek Granite, the Whitney Granodiorite, the Johnson Granite Porphyry, and the Golden Bear Dike. Megacrysts in these igneous bodies attain 4-10 cm in length. All have sawtooth oscillatory zoning marked by varying concentration of BaO ranging generally from 3.5 to 0.5 wt%. Some of the more pronounced zones begin with resorption and channeling of the underlying zone. Layers of mineral inclusions, principally plagioclase, but also biotite, quartz, hornblende, titanite, and accessory minerals, are parallel to the BaO-delineated zones, are sorted by size along the boundaries, and have their long axes preferentially aligned parallel to the boundaries. These features indicate that the K-feldspar megacrysts grew while surrounded by melt, allowing the inclusion minerals to periodically attach themselves to the faces of the growing crystals. The temperature of growth of titanite included within the K-feldspar megacrysts is estimated by use of a Zr-in-titanite geothermometer. Megacryst-hosted titanite grains all yield temperatures typical of felsic magmas, mainly 735-760 ??C. Titanite grains in the granodiorite hosts marginal to the megacrysts range to lower growth temperatures, in some instances into the subsolidus. The limited range and igneous values of growth temperatures for megacryst-hosted titanite grains support the interpretation that the megacrysts formed ag igneous sanidine phenocrysts, that intrusion temperatures varied by only small amounts while the megacrysts grew, and that megacryst growth ceased before the intrusions cooled below the solidus. Individual Ba-enriched zones were apparently formed by repeated surges of new, hotter granitic melt that replenished these large magma chambers. Each recharge of hot magron offset cooling, maintained the partially molten or mushy character of the chamber, stirred up crystals, and induced convective currents that lofted, settling megacrysts back up into the chamber. Because of repeated reheating of the magma chamber and prolonged maintenance of the melt, this process apparently continued long enough to provide the ideal environment for the growth of these extraordinarily large K-feldspar phenocrysts. ??2008 Geological Society of America.

Greenstone-hosted lode-gold mineralization at Dungash mine, Eastern Desert, Egypt

NASA Astrophysics Data System (ADS)

Zoheir, Basem; Weihed, Pär

2014-11-01

The auriferous quartz ± carbonate veins at Dungash mine, central Eastern Desert of Egypt, are confined to ∼E-trending dilation zones within variably foliated/sheared metavolcanic/volcaniclastic rocks. The vein morphology and internal structures demonstrate formation concurrent with a dextral shear system. The latter is attributed to flexural displacement of folded, heterogeneous rock blocks through transpression increment, late in the Neoproterozoic deformation history of the area. Geochemistry of the host metavolcanic/metavolcaniclastic rocks from the mine area suggests derivation from a low-K, calc-alkaline magma in a subduction-related, volcanic arc setting. In addition, chemistry of disseminated Cr-spinels further constrain on the back-arc basin setting and low-grade metamorphism, typical of gold-hosting greenstone belts elsewhere. Mineralogy of the mineralized veins includes an early assemblage of arsenopyrite-As-pyrite-gersdorffite ± pyrrhotite, a transitional pyrite-Sb-arsenopyrite ± gersdorffite assemblage, and a late tetrahedrite-chalcopyrite-sphalerite-galena-gold assemblage. Based on arsenopyrite and chlorite geothermometers, formation of gold-sulfide mineralization occurred between ∼365 and 280 °C. LA-ICP-MS measurements indicate the presence of refractory Au in arsenian pyrite (up to 53 ppm) and Sb-bearing arsenopyrite (up to 974 ppm). Abundant free-milling gold associated with the late sulfide assemblage may have been mobilized and re-distributed by circulating, lower temperature ore fluids in the waning stages of the hydrothermal system. Based on the isotopic values of vein quartz and carbonate, the calculated average δ18OH2O values of the ore fluids are 5.0 ± 1.4‰ SMOW for quartz, and 3.3 ± 1.4‰ for vein carbonate. The measured carbonate δ13C values correspond to ore fluids with δ13CCO2 = -6.7 ± 0.7‰ PDB. These results suggest a mainly metamorphic source for ore fluids, in good agreement with the vein morphology, textures and hydrothermal alteration. The calculated δ34SH2S values for early, transitional, and late sulfide assemblages define three distinct ranges (∼1.5-3.6‰), (∼0.4-1.0‰), and (-3.7‰ to -1.9‰), respectively. The systematic evolution towards lighter δ34S values may be attributed to recrystallization, or to ore fluid buffering under variable physicochemical conditions. The shear zone-related setting, mineralogy and isotopic characteristics of gold mineralization in Dungash mine are comparable with other orogenic gold deposits in the region (e.g., Barramiya deposit), which may suggest a regional setting controlling gold metallogeny of the region. This setting should guide future exploration programs in the central Eastern Desert province.

Kyanite-garnet gneisses of the Kåfjord Nappe - North Norwegian Caledonides: P-T conditions and monazite Th-U-Pb dating

NASA Astrophysics Data System (ADS)

Ziemniak, Grzegorz; Kośmińska, Karolina; Majka, Jarosław; Janák, Marian; Manecki, Maciej

2016-04-01

The Kåfjord Nappe is the part of the Skibotn Nappe Complex traditionally ascribed to the Upper Allochthon of the North Norwegian Caledonides. Pressure-temperature (P-T) conditions and metamorphic age of the Kåfjord Nappe are not well constrained, geochronological data are limited to a single Rb-Sr age of c. 440 Ma (Dangla et al. 1978). Metamorphic evolution of kyanite-garnet gneisses of the Kåfjord Nappe is presented here. The kyanite-garnet gneisses are associated with a few meters thick amphibolite lenses. The gneisses mainly consist of quartz, plagioclase, biotite, muscovite, garnet, kyanite, and rutile. Retrograde minerals are represented by sillimanite and chlorite. Garnet occurs as two textural types. Garnet-I forms euhedral porphyroblasts with multiple small inclusions. Profiles through garnet-I show chemical zonation in all components. The composition varies from Alm64-68Prp11-16Grs13-18Sps2-8 in the core to Alm68-70Prp17-18Grs10-13Sps1-3 in the rim. Garnet-II is subhedral to anhedral, its core is inclusion-rich, whereas rim contains only single inclusions. Chemical composition of garnet-II is similar to that of the garnet-I rim. P-T conditions have been estimated using the garnet-biotite-muscovite-plagioclase (GBPM) geothermobarometer (Holdaway, 2001; Wu, 2014). Calculated peak P-T metamorphic conditions are 610-625 °C and 7.6-8.2 kbar corresponding to the amphibolite facies conditions. Phase equilibrium modelling in the NCKFMMnASH system yields peak metamorphic conditions of c. 620 °C at 8 kbar. Growth conditions of garnet-I core modelled in the NCKFMMnASH system are c. 570 °C at 9.7 kbar. Chemical Th-U-total Pb monazite dating has been performed. Preliminary dating results from the kyanite-garnet gneiss of the Kåfjord Nappe yield an array of dates from 468 Ma to 404 Ma. There is a correlation between an increase of yttrium content and decrease of monazite single dates. Compositional maps confirm an increase of yttrium towards the rim of the monazite. This work is partially funded by AGH research grant no 11.11.140.319. References: Dangla, P., Damange, J. C., Ploquin, A., Quarnadel, J. M., Sonet, J., 1978. Donn'es geochronlogiques sur les Caledonides Scandinaves septentrionates (Troms, Norway du Nord). C. r. Acad. Sci. Paris, 286 D, 1653-1656. Holdaway, M. J., 2001. Recalibration of the GASP geobarometer in light of recent garnet and plagioclase activity models and versions of the garnet-biotite geothermometer. American Mineralogist, 86(10), 1117-1129. Wu, C. M., 2015. Revised empirical garnet-biotite-muscovite-plagioclase geobarometer in metapelites. Journal of Metamorphic Geology, 33(2), 167-176.

Petrologic evidence that most ocean islands derive from thermally driven mantle plumes

NASA Astrophysics Data System (ADS)

Putirka, K. D.

2006-12-01

Perhaps the most crucial test of the mantle plume hypothesis concerns whether hot spots are indeed hot. To conduct this test, olivine-liquid equilibria are used to estimate mantle potential temperatures (Tp) for 15 putative plume localities (using the GEOROC database). Ocean islands (OIB) were selected on the availability of rocks that attain olivine control (where olivine addition/removal alone controls rock composition) so that primitive FeO contents could be estimated. Several other variables in addition to FeO must also be known: Except at Iceland and Hawaii, where large numbers of olivine analyses allow individual estimates for the maximum forsterite contents (Fomax) of olivines, a single Fomax value, 91.5, is adopted for all OIB (and MORB; determined from a global database of olivine compositions); as a null hypothesis, MORB-like values for oxygen fugacity (QFM-1; Bezos and Humler, 2005) and the Fe-Mg exchange coefficient between olivine and liquid (0.31; calculated from Toplis, 2005, Herzberg and O'Hara, 1998) are adopted. Generalized differences in water contents between OIB and MORB (Dixon et al., 2002) are also accounted for. All temperatures are calculated at 1 GPa, using averages of existing (Beattie, 1993) and new (Putirka et al., 2006) olivine geothermometers. Except for Galapagos, primitive OIBs have nearly uniform FeO contents that are higher compared to MORB (at MgO>10 wt. %, mean OIB FeOt = 11.6 wt. %). These high FeO contents require higher mean temperatures of olivine-liquid equilibration for OIB, by an average of 150±20°C compared to MORB. Olivine equilibration temperatures do not depend on mantle source composition, so are independent of whether eclogite-type components occur in the mantle. If a peridotite bulk composition is assumed (to estimate melt fraction from partial melting experiments) olivine equilibration temperatures can be converted to Tp; OIB (Galapagos excepted) yield a mean Tp of 1583°C, compared to 1397°C for MORB. When inter- island compositional variation is accounted for, all OIB except Galapagos yield excess temperatures (Tp^{OIB} - Tp^{MORB}) of 133-280°C, with a mean of 186± 36°C. Galapagos lavas yield an excess temperature of 16°C; perhaps mixing has diluted its thermal signal, but in any event, its Tp is essentially identical to MORB. Nevertheless, most OIB (93% in this sample) exhibit large excess temperatures. Thermally driven mantle plumes, as proposed by Morgan (1971), thus appear to be common, not rare. A second implication, less certain than the first, involves the narrow standard deviation of ±36°C for Tp at OIB, which almost certainly reflects a lower limit to actual thermal variability. This narrow range indicates that all hot spots derive from a single thermal boundary layer.

Are ``Hot Spots'' Hot? - An Overview

NASA Astrophysics Data System (ADS)

Foulger, G. R.

2010-12-01

The term “hot spot” is taken variously to imply a) the presence of excessive volcanism, or b) that the melt formed in an unusually hot source. Case b) is intrinsic to the plume hypothesis. Temperature anomalies of 200-300 degrees Celsius are expected, though there is widespread downward-revision of this where observations do not support it. It is not self-evident that “hot spots” are hot in the sense of case b), despite the fact that this is widely assumed. Furthermore, a hot source is not strongly supported by observations, and is at odds with many data. The temperature of the mantle has been studied using many different methods. Global oceanic heat flow values were recently assessed, but reveal no evidence for elevated temperatures around proposed plume localities. Mapping surface heat flow is only sensitive to anomalies at the level of 100 degrees Celsius, however. Seismological methods include correlating velocity with crustal thickness at LIPs, measuring transition zone thickness, and mapping velocity, e.g., using tomography. The first of these does not find evidence for elevated temperatures. The latter two are both sensitive to the presence of partial melt and variations in rock composition, in addition to temperature, which is the weakest potential effect. They thus cannot be used as thermometers. In particular, it cannot be assumed that red = hot and blue = cold in tomographic cross sections. Petrological and geochemical approaches include the “global systematics”. This has now been shown to not work for estimating temperature and its application should be discontinued. Mineralogical phase relationships are applied by comparing data from laboratory melting experiments to observations. Olivine control-line analysis has been extensively used in attempts to measure the differences in melt-formation temperature between mid-ocean ridges and melting anomalies. Difficulties arise in choosing the correct olivine geothermometer and because picrite glass is lacking from any melting anomaly except Hawaii. The results must be compared with a measure of the temperature of “normal mantle”. This is usually taken to be the temperature of melt formation beneath mid-ocean ridges, but the correct choice is controversial. Furthermore, this cannot be assumed to represent the potential temperature of the mantle in general. The surface conduction layer may extend much deeper than the depth of extraction of MORB, so melt extracted from greater depths, e.g., from beneath the base of the lithosphere in old parts of the ocean basins, may form at higher temperatures. It is easier to assume that the mantle beneath “hot spots” is hot than it is to show unequivocally that it is true. This endeavor is perhaps the most direct way of testing the plume hypothesis, but it is also one of the most challenging.

Yttrium geothermometry: an approach to determine the oldest garnet growth recrystallization conditions from micaschists (Yunquera Unit, Betic Cordilleras, southern Spain

NASA Astrophysics Data System (ADS)

Esteban, J. J.; Cuevas, J.; Tubía, J. M.; Gil Ibarguchi, J. I.

2012-04-01

The garnet-xenotime geothermometry is nowadays been using as a tool to identify low-grade relic garnets and even to calculate garnet growth temperatures in metapelites that have undergone a polymetamorphic evolution (Pyle and Spear, 2000; Borghi et al., 2006). A prograde metamorphic evolution, under continuously increasing temperature, can induce garnet and accompanying phase's composition homogenization by intra-crystalline diffusion, leading to flat zoning profiles. Consequently, the application of conventional geothermobarometers on those mineral assemblages does establish minimum P-T conditions. Therefore, the less susceptible elements to diffusion processes, like trace elements, should be taken into account in order to reconstruct their metamorphic evolution. We studied a polymetamorphic micaschist recovered from the Yunquera Unit, one of the tectonic slices of the Internal Zone of the Betic Cordilleras (southern Spain) (Dürr, 1963). The Yunquera unit evidences three stages of recrystallization at different P-T conditions. According to conventional geothermobarometry (Esteban et al., 2005) the metamorphic peak, M2, is estimated at 1200-1300 MPa and 560-695 °C and the decompression path, M3, at 600 MPa and 700 °C. The lack of mineral paragenesis in apparent chemical equilibrium during M1, does not allow determining accurately its recrystallization conditions. Xenotime, identified by scanning electron microprobe, appears as matrix mineral and therefore the entire garnets are assumed to be in chemical equilibrium with it. Yttrium profiles of two garnets show a mean bell-shape compositional variation that differs significatively from the discontinuous profiles shown by Ca, Mg and Fe. This difference accounts for different diffusion rates for those elements and agree with the original Y-zoning preservation. A third Y-profile shows an oscillatory compositional variation. The internal part of garnets, bounded by sharp inclusion trails, are characterized by sawed bell-shape zoning in the range of ca. 500-2000 ppm of Y, that abruptly decreases to less than 500 ppm to the borders. Temperature distribution calculated from the garnet-xenotime geothermometer of Pyle and Spear (2000) is outlined by flat patterns, matching up with the cores of the garnets, and by a slightly increase to the rim. The metamorphic temperature calculated using the Y-concentration of the central portions of garnet cores is ca. 520 °C, whereas towards the rim the temperature does increase up to ca. 575-625 °C. The estimation of garnet recrystallization pressure is still a matter of discussion, furthermore when the hypothetical equilibrium paragenesis is absent. According to the presented data, we suggest that the oldest garnet growth generation did occur at ca. 520 °C and therefore, the preservation of original Y-zonings can be used for thermal history reconstructions, as Y-content in garnet is T-dependent.

Back arc basalts from Patagonia: sediment input in a distal subduction domain

NASA Astrophysics Data System (ADS)

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

2007-12-01

Cinder cones and lava flows from the Loncopue graben in N Patagonia (37 S) were sampled over a 180 km N-S transect. These mainly basaltic and trachybasaltic lava flows carry olivine with Cr-Al-rich spinel inclusions, while some more evolved flows carry clinopyroxene and plagioclase. Most of these rocks have between 5-8 percent MgO, and show highly variable K and LIL trace element concentrations. The rocks have up to 180 ppm Ni and 250 ppm Cr. Relative trace element abundance diagrams show negative Ta-Nb anomalies in most rocks, although their depths vary strongly. The REE patterns show LREE enrichment and most rocks have no Eu anomalies, indicating the absence of significant plagioclase fractionation. The basalts have constant U/Th values (~0.25) that are similar to those found in the nearby Copahue-Caviahue arc volcanics. Microprobe analyses of the main phases show olivine with Mg # of 80-87 and up to 2600 ppm Ni. Simulations with the Melts-pMelts programs and application of mineral-melt geothermometers suggest that most olivine phenocrysts crystallized at ~8-10 kbar pressure at temperatures of 1170-1220 oC and with 1-3 percent H2O in the melt. The Sr isotope compositions of 9 samples show a range from 0.7033 - 0.7043, which are negatively correlated with Nd isotope ratios (0.51273- 0.51292). Surprisingly, the most MgO-rich basalt has the most radiogenic Sr isotope ratio. The Pb isotope ratios, well outside the DMM range, correlate very poorly with either Sr isotope ratios or in Pb-Pb isotope graphs. The lack of correlation between degree of evolution and Sr isotope ratios as well as the primitive nature of the rocks and crystals suggest that crustal assimilation was not a major process impacting the composition of these small magma volumes. Incompatible trace element patterns of several samples resemble those of detrital sediment samples from the Pacific, which together with the isotopic data suggest that these magmas may carry a subducted sediment component. Trace element concentrations and ratios do not correlate with radiogenic isotope ratios, suggesting that more than one contaminant source impacted the mantle domain, e.g., fluids as well as sediment melts. Isotope and trace element ratios vary considerably between cinder cones that are only 10-15 km apart, suggesting that the underlying mantle is highly heterogeneous, enriched in subducted components in thin veins and patches. The Loncopue basalts seem to be transitional in composition between the very voluminous S-Patagonia back-arc basalts and the Copahue-Caviahue arc rocks to the north.

Data integration and conceptual modelling of the Larderello geothermal area, Italy

NASA Astrophysics Data System (ADS)

Manzella, Adele; Gola, Gianluca; Bertini, Giovanni; Bonini, Marco; Botteghi, Serena; Brogi, Andrea; De Franco, Roberto; Dini, Andrea; Donato, Assunta; Gianelli, Giovanni; Liotta, Domenico; Montanari, Domenico; Montegrossi, Giordano; Petracchini, Lorenzo; Ruggieri, Giovanni; Santilano, Alessandro; Scrocca, Davide; Trumpy, Eugenio

2017-04-01

The Larderello geothermal field, located in southern Tuscany (Italy), is one of the most important long-living hydrothermal system in the world. The inner zone of the Northern Apennines is characterized by high heat flow, well constrained by several hundred measurements deriving from both shallow boreholes and deep exploration wells. It is widely accepted that the interplay among extensional tectonics, thinning of the previously overthickened crust and lithosphere, and magmatism related to crustal melting and hybridism, controlled the NW-SE trending geothermal anomaly occurring in southern Tuscany. At Larderello, the geothermal exploitation started at the beginning of the last century from the shallow evaporite-carbonate reservoir (about 700 - 1000 m b.g.l. on average) hosting a super-heated steam with temperature ranging from 150°C to 260°C. A deep exploration program was carried out in the early 1980s. Deep boreholes found a super-heated steam-dominated system hosted in the metamorphic basement (about 2500 - 4000 m b.g.l), characterized by temperatures ranging from 300°C to 350°C. In the SW part of the Larderello area (Lago locality), a temperature exceeding 400°C was measured down to 3000 m b.s.l. The 2D and 3D seismic exploration activities provided evidences of a seismic marker, locally showing bright spot features, defining the top of a deeper reflective crustal interval, named as "K-horizon". The K-horizon has not yet been drilled, but some boreholes approached it. This seismic reflector exhibits interesting positive correlation with the maximum peak of the hypocentre distribution of low-magnitude earthquakes and, at the same time, its shape coincides with the thermal anomaly distribution, in plain view. The review and updating of the velocity and resistivity models suggest the existence of over-pressurized fluids, likely of magmatic and/or thermo-metamorphic origin, which originate the seismic velocity anomalies. The upward migration and storage of the fluids can be controlled by: i) structural conduits crossing a multi-layered crust affected by magmatic intrusions; ii) mechanisms controlling the fluid migration in different rheological settings; and iii) self-sealing processes of magmatic hypersaline fluids arising from the brittle/ductile transition. Our study is addressed to the better understanding of the structure of the deepest part of the Larderello geothermal field, by integrating structural, geological, geochemical and geophysical data. Based on downward temperature extrapolation, fluid inclusions and geothermometers analyses, the possible occurrence of super-hot fluids, in supercritical conditions, nearby the K-horizon is envisaged. The final goal is to achieve a comprehensive understanding of the geological structure and the physical conditions (pressure and temperature) of the deep reservoir including also the zone corresponding to the K-horizon, to characterize the supercritical geothermal system as well as the deep crustal processes that work in synergy leading to the regional anomaly.

The Pinkie Unit of the Southwestern Svalbard Caledonian Province and its bearing on distribution of the Torellian-Timanian basement in the High Arctic

NASA Astrophysics Data System (ADS)

Kośmińska, Karolina; Majka, Jarosław; Manecki, Maciej

2015-04-01

Here we present for the first time petrological characteristics of metapelites from the Pinkie Unit (Prins Karls Forland, western Svalbard). Rocks belonging to the Pinkie Unit are represented mainly by laminated quartzites, siliciclastic rocks (sometimes with garnet) and garnet-bearing mica schists. They are overthrust by the lower grade lithologies of the Grampian Group. The mineral composition confirmed by preliminary microscopic observations suggests that the Pinkie rocks were subjected to at least amphibolite facies metamorphism. The metamorphic zoning from chloritoid through staurolite, up to kyanite zone is apparent. This indicates Barrovian type metamorphism. The rocks are strongly deformed, M1 assemblages and D1 structures are overprinted by pervasive D2 mylonitic pattern. This study is focused on kyanite-bearing schists. They consist mainly of garnet, plagioclase, biotite, muscovite, kyanite, quartz and turmaline. Garnet forms anhedral crystals. Its chemical composition is characterized by Alm79-84Sps1-5Prp5-11Grs5-10. The profiles through the garnets are almost flat and they seem to be homogenized most probably during peak temperature at an early stage of retrogression. The Si content in muscovite varies from 3.06 to 3.13. Biotite is characterized by XFe in the range of 0.53 - 0.66. The garnet-biotite-muscovite-plagioclase (GBPM) geothermobarometer (Holdaway, 2001; Wu, 2014) has been used for estimation of pressure - temperature conditions. Preliminary calculations indicate peak metamorphic conditions at 8 - 9 kbar and 650 - 700°C. Our P-T calculations provide further evidence for the Barrovian type of metamorphism along the western coast of Svalbard. The correlation of the Pinkie Unit with other higher grade complexes within Southwestern Svalbard Caledonian Province is still difficult, but the studied rocks resemble the Isbjørnhamna Group of Wedel Jarlsberg Land. This is based on the metamorphic grade, mineral assemblage and probable protolith age (post-950Ma; Kośmińska, unpublished data). If this is a case, the Pinkie Unit will provide another evidence of the Torellian-Timanian (late Neoproterozoic, e.g. Majka et al. 2008) tectonothermal event within the Svalbard's Caledonides. In turn, it can bear important implications for Arctic tectonic reconstructions. This project is financed by NCN research project No 2013/11/N/ST10/00357. References: Holdaway M.J., 2001. Recalibration of the GASP geobarometer in light of recent garnet and plagioclase activity models and versions of the garnet-biotite geothermometer. American Mineralogist, 86, 1117-1129. Majka J., Mazur S., Czerny J., Manecki M., Holm D.K., 2008. Late Neoproterozoic amphibolite facies metamorphism of a pre-Caledonian basement block in southwest Wedel Jarlsberg Land, Spitsbergen: new evidence from U-Th-Pb dating of monazite. Geological Magazine, 145, 822-830. Wu C. M., 2014. Revised empirical garnet-biotite-muscovite-plagioclase (GBMP) geobarometer in metapelites. Journal of Metamorphic Geology. doi: 10.1111/jmg.12115

The Origin of Carbon-bearing Volatiles in Surprise Valley Hot Springs in the Great Basin: Carbon Isotope aud Water Chemistry Characterizations

NASA Technical Reports Server (NTRS)

Fu, Qi; Socki, Richard A.; Niles, Paul B.; Romanek, Christopher; Datta, Saugata; Darnell, Mike; Bissada, Adry K.

2013-01-01

There are numerous hydrothermal fields within the Great Basin of North America, some of which have been exploited for geothermal resources. With methane and other carbon-bearing compounds being observed, in some cases with high concentrations, however, their origins and formation conditions remain unknown. Thus, studying hydrothermal springs in this area provides us an opportunity to expand our knowledge of subsurface (bio)chemical processes that generate organic compounds in hydrothermal systems, and aid in future development and exploration of potential energy resources as well. While isotope measurement has long been used for recognition of their origins, there are several secondary processes that may generate variations in isotopic compositions: oxidation, re-equilibration of methane and other alkanes with CO2, mixing with compounds of other sources, etc. Therefore, in addition to isotopic analysis, other evidence, including water chemistry and rock compositions, are necessary to identify volatile compounds of different sources. Surprise Valley Hot Springs (SVHS, 41º32'N, 120º5'W), located in a typical basin and range province valley in northeastern California, is a terrestrial hydrothermal spring system of the Great Basin. Previous geophysical studies indicated the presence of clay-rich volcanic and sedimentary rocks of Tertiary age beneath the lava flows in late Tertiary and Quaternary. Water and gas samples were collected for a variety of chemical and isotope composition analyses, including in-situ pH, alkalinity, conductivity, oxidation reduction potential (ORP), major and trace elements, and C and H isotope measurements. Fluids issuing from SVHS can be classified as Na-(Cl)-SO4 type, with the major cation and anion being Na+ and SO4 2-, respectively. Thermodynamic calculation using ORP and major element data indicated that sulfate is the most dominant sulfur species, which is consistent with anion analysis results. Aquifer temperatures at depth estimated by both dissolved SiO2 and Na-K-Ca geothermometers are in the range of 125.0 to 135.4 oC, and higher than the values measured at orifices (77.3 to 90.0 oC). CO2 and homologs of straight chain alkanes (C1-C5) were identified in gas samples. Carbon isotope values of alkanes increase with carbon numbers. The 13C fractionation between CO2 and dissolved inorganic carbon suggests they are out of carbon isotope equilibrium. The hypothesis regarding the formation of carbon-bearing compounds in SVHS may involve two processes: 1) Under high heat flow conditions which are caused by regional faulting and crustal extension, original high molecular weight organic compounds (kerogens) in clay-rich rocks decomposed to generate methane and other alkane homologs. 2) The SVHS area is associated with outflow structures, and distant from the heat source. Anaerobic oxidation of methane (AOM) with sulfate at shallow depth (< 90 oC) is suggested as being responsible for the generation of CO2 in SVHS.

The Origin of Carbon-bearing Volatiles in Surprise Valley Hot Springs in the Great Basin: Carbon Isotope and Water Chemistry Characterizations

NASA Technical Reports Server (NTRS)

Fu, Qi; Socki, Richard A.; Niles, Paul B.; Romanek, Christopher; Datta, Saugata; Darnell, Mike; Bissada, Adry K.

2013-01-01

There are numerous hydrothermal fields within the Great Basin of North America, some of which have been exploited for geothermal resources. With methane and other carbon-bearing compounds being observed, in some cases with high concentrations, however, their origins and formation conditions remain unknown. Thus, studying hydrothermal springs in this area provides us an opportunity to expand our knowledge of subsurface (bio)chemical processes that generate organic compounds in hydrothermal systems, and aid in future development and exploration of potential energy resources as well. While isotope measurement has long been used for recognition of their origins, there are several secondary processes that may generate variations in isotopic compositions: oxidation, re-equilibration of methane and other alkanes with CO2, mixing with compounds of other sources, etc. Therefore, in addition to isotopic analysis, other evidence, including water chemistry and rock compositions, are necessary to identify volatile compounds of different sources. Surprise Valley Hot Springs (SVHS, 41 deg 32'N, 120 deg 5'W), located in a typical basin and range province valley in northeastern California, is a terrestrial hydrothermal spring system of the Great Basin. Previous geophysical studies indicated the presence of clay-rich volcanic and sedimentary rocks of Tertiary age beneath the lava flows in late Tertiary and Quaternary. Water and gas samples were collected for a variety of chemical and isotope composition analyses, including in-situ pH, alkalinity, conductivity, oxidation reduction potential (ORP), major and trace elements, and C and H isotope measurements. Fluids issuing from SVHS can be classified as Na-(Cl)-SO4 type, with the major cation and anion being Na+ and SO4(2-), respectively. Thermodynamic calculation using ORP and major element data indicated that sulfate is the most dominant sulfur species, which is consistent with anion analysis results. Aquifer temperatures at depth estimated by both dissolved SiO2 and Na-K-Ca geothermometers are in the range of 125.0 to 135.4 C, and higher than the values measured at orifices (77.3 to 90.0 C). CO2 and homologs of straight chain alkanes (C1-C5) were identified in gas samples. Carbon isotope values of alkanes increase with carbon numbers. The C-13 fractionation between CO2 and dissolved inorganic carbon suggests they are out of carbon isotope equilibrium. The hypothesis regarding the formation of carbon-bearing compounds in SVHS may involve two processes: 1) Under high heat flow conditions which are caused by regional faulting and crustal extension, original high molecular weight organic compounds (kerogens) in clay-rich rocks decomposed to generate methane and other alkane homologs. 2) The SVHS area is associated with outflow structures, and distant from the heat source. Anaerobic oxidation of methane (AOM) with sulfate at shallow depth (< 90 C) is suggested as being responsible for the generation of CO2 in SVHS.

Magnesium isotope fractionation in co-existing clino-pyroxene and garnet: implications for geothermometry and mantle source characterization

NASA Astrophysics Data System (ADS)

Chakrabarti, R.; Jacobsen, S. B.; Basu, A. R.

2011-12-01

It is now well established that the Mg isotopic composition of the bulk silicate Earth, as represented by olivines, peridotites and basalts is identical to bulk meteorites and the Moon. However, small differences have been documented between co-existing olivines and clino-pyroxenes in mantle xenoliths as well as co-existing hornblendes and biotites in granitoids; spinels show some of the heaviest δ26Mg (deviation of the 26Mg/24Mg ratio from the Dead Sea Metal standard). A recent study has documented a large Mg isotopic fractionation between co-existing omphacite and garnet (Δ26MgOMP-GT = δ26MgOMP - δ26MgGT ~1.14) from eclogites in the Dabie orogen of China. This large equilibrium Mg isotope fractionation is explained by the difference in coordination number of Mg in omphacite (six) and garnet (eight). We report stable Mg isotopic compositions of co-existing garnet and clino-pyroxenes from different mantle-derived rocks. Garnet-omphacite pairs analyzed are from an eclogite xenolith from the Roberts Victor kimberlite pipe, the ultra-high pressure Tso Morari eclogite from the Ladakh Himalayas and the Healdsburg eclogite from the Franciscan Subduction Complex, which have a wide range in estimated temperatures of equilibration. Although, the latter two eclogites were exhumed in orogenic belts, our selective picking of the mineral cores for analysis avoided retrograded compositions. We have also analyzed Cr-diopside and pyrope-rich garnet pairs from several southern African kimberlite pipes. These include granular garnet peridotite xenoliths (P = 30-40 kbar, T =950-10500C) as well as the deeper sheared xenoliths (P = 50-60 kbar, T = 13500C). Rapid quenching of the kimberlite-hosted xenoliths ensures minimal low temperature pervasive alteration of these samples. Also analyzed are samples from the Gore Mt. amphibolite and a wollastonite-diopside-garnet skarn from the Adirondacks with equilibration temperatures of 700-7260C. Minerals were separated by hand-picking under a binocular microscope. Mg was quantitatively separated from other matrix elements using cation exchange chromatography. All three Mg isotopes were simultaneously measured using the IsoProbe-P MC-ICPMS at Harvard University by sample-standard bracketing. Our results from 11 garnet-clinopyroxene mineral pairs with widely varying temperatures of equilibration indicate that δ26Mg in garnet (-0.6 to -2.3) is much lower than that in co-existing clino-pyroxenes (-0.1 to -0.6 and -1.3 in the wollastonite skarn). This result is consistent with theoretical predictions as well as recent results from the Dabie orogen. Δ26Mg between clino-pyroxene and garnet ranges from 0.7 to 2.3. Our results suggest a temperature dependence of Δ26Mg between clino-pyroxene and garnet in mantle-derived rocks which can potentially be used as a geothermometer. Large Mg isotopic fractionation between co-existing garnet and clino-pyroxenes has implications for source characterization (garnet peridotite versus eclogite) of mantle-derived melts.

High-temperature carbonates in the Stillwater Complex, Montana, USA

NASA Astrophysics Data System (ADS)

Aird, H. M.; Boudreau, A. E.

2012-12-01

The processes involved in the petrogenesis of the sulphide-hosted platinum-group-element (PGE) deposits of the Stillwater Complex are controversial, with theories ranging from the purely magmatic to those involving an aqueous fluid. To further constrain these models, we have been examining the trace phase assemblages in rocks away from the ore zones. High-temperature carbonates have been observed in association with sulphide minerals below the platiniferous J-M Reef of the Stillwater Complex. The carbonate assemblage consists of dolomite with exsolved calcite and is found in contact with sulphide minerals: chalcopyrite and pyrrhotite in the Peridotite Zone; and pyrrhotite with pentlandite, pyrite and chalcopyrite in Gabbronorite I of the Lower Banded Series. The minimal silicate alteration and the lack of greenschist minerals in association with the mineral assemblage are consistent with a high-temperature origin for the carbonates. The calcite-dolomite geothermometer [1] yields a minimum formation temperature of ~900°C for the unmixed assemblages. A reaction rim surrounds the carbonate-sulphide assemblages, showing an alteration of the host orthopyroxene to a more Ca-enriched, Fe-depleted composition. This is consistent with diffusive exchange between carbonates and pyroxenes at high temperatures, mediated by an aqueous fluid. The highly variable molar MnO/FeO ratios in both the high-temperature carbonates and their associated altered pyroxene rims also imply their interaction with a fluid. The carbonate assemblages are consistent with Stillwater fluid inclusion studies [2], showing that fluids comprising coexisting Cl-rich brine and carbonic fluid were trapped in pegmatitic quartz at 700-715°C, some of which also contained "accidental" calcite inclusions. The high Cl-content of apatite [3] found below the platiniferous J-M Reef is further evidence that a Cl-rich fluid was migrating through the rocks beneath the Reef. Carbonates have been shown to be stabilized by Cl-rich fluids [4]. The association of high-temperature carbonates with sulphides beneath the J-M reef supports the hydromagmatic theory which involves a late-stage chloride-carbonate fluid percolating upwards, dissolving PGE and sulphides and redepositing them at a higher stratigraphic level. [1] Anovitz, L.M., and Essene, E.J., 1987, Phase Equilibria in the System CaCO3-MgCO3-FeCO3: Journal of Petrology, v. 28, p. 389-414. [2] Hanley, J.J., Mungall, J.E., Pettke, T., Spooner, E.T.C., and Bray, C.J., 2008, Fluid and Halide Melt Inclusions of Magmatic Origin in the Ultramafic and Lower Banded Series, Stillwater Complex, Montana, USA: Journal of Petrology, v. 49, p. 1133-1160. [3] Boudreau, A.E., and McCallum, I.S., 1989, Investigations of the Stillwater Complex: Part V. Apatites as indicators of evolving fluid composition: Contributions to Mineralogy and Petrology, v. 102, p. 138-153. [4] Newton, R.C., and Manning, C.E., 2002, Experimental determination of calcite solubility in H2O-NaCl solutions at deep crust/upper mantle pressures and temperature: implications for metasomatic processes in shear zones: American Mineralogist, v. 87, p. 1401-1409.

Incipient rifting accompanied by the release of subcontinental lithospheric mantle volatiles in the Magadi and Natron basin, East Africa

NASA Astrophysics Data System (ADS)

Lee, Hyunwoo; Fischer, Tobias P.; Muirhead, James D.; Ebinger, Cynthia J.; Kattenhorn, Simon A.; Sharp, Zachary D.; Kianji, Gladys; Takahata, Naoto; Sano, Yuji

2017-10-01

Geochemical investigations of volatiles in hydrothermal systems are used to understand heat sources and subsurface processes occurring at volcanic-tectonic settings. This study reports new results of gas chemistry and isotopes (O, H, N, C, and He) of thermal spring samples (T = 36.8-83.5 °C; pH = 8.5-10.3) from the Magadi and Natron basin (MNB) in the East African Rift (EAR). Although a number of thermal springs are shown to ascend along normal faults and feed into major lakes (Magadi, Little Magadi, and Natron), volatile sources and fluxes of these fluids are poorly constrained. CO2 is the most abundant phase (up to 996.325 mmol/mol), and the N2-He-Ar abundances show a mixture of dissolved gases from deep (mantle-derived) and shallow (air/air saturated water) sources. The H2-Ar-CH4-CO2 geothermometers indicate that equilibrium temperatures range from 100 to 150 °C. δ18O (- 4.4 to - 0.2‰) and δD (- 28.9 to - 3.9‰) values of the MNB thermal waters still lie slightly to the right of the local meteoric water lines, reflecting minor evaporation. Each mixing relationship of N2 (δ15N = - 1.5 to 0.4‰; N2/3He = 3.92 × 106-1.33 × 109, except for an anomalous biogenic sample (δ15N = 5.9‰)) and CO2 (δ13C = - 5.7 to 1.6‰; CO2/3He = 7.24 × 108-1.81 × 1011) suggests that the predominant mantle component of the MNB volatiles is Subcontinental Lithospheric Mantle (SCLM). However, N2 is mostly atmospheric, and minor CO2 is contributed by the limestone end-member. 3He/4He ratios (0.64-4.00 Ra) also indicate a contribution of SCLM (R/Ra = 6.1 ± 0.9), with radiogenic 4He derived from a crustal source (R/Ra = 0.02). The MNB 4He flux rates (3.64 × 1011 to 3.34 × 1014 atoms/m2 s) are significantly greater than the reported mean of global continental flux values (4.18 × 1010 atoms/m2 s), implying that magma intrusions could supply mantle 4He, and related heating and fracturing release crustal 4He from the Tanzanian craton and Mozambique belt. Total flux values (mol/yr) of 3He, N2, and CO2 are 8.18, 4.07 × 107, and 5.31 × 109, which are 1.28%, 2.04%, and 0.24% of global fluxes, respectively. Our results suggest that the primary source of magmatic volatiles in the MNB is SCLM, with additional crustal contributions, which is different from the KRV volatiles that have more asthenospheric mantle components. Volatiles from SCLM in magmas stall in the crust to heat and fracture country rock, with accompanying crustal volatile release. These volatile signatures reveal that MORB-type mantle replaces a relatively small volume of SCLM during incipient rifting (< 10 Ma) in the EAR.

Variations in Melt Generation and Migration along the Aleutian Arc (Invited)

NASA Astrophysics Data System (ADS)

Plank, T. A.; Van Keken, P. E.

2013-12-01

The generation and ascent of mantle melt beneath volcanic arcs sets the course for how magmas differentiate to form the continental crust and erupt explosively from volcanoes. Although the basic framework of melting at subduction zones is understood to involve the convective influx of hot mantle (Tp ≥ 1300°C) and advective transport of water-rich fluids from the subducting slab, the P-T paths that melts follow during melt generation and migration are still not well known. The Aleutian Arc provides an opportunity to explore the conditions of mantle melting in the context of volcanoes that span an unusually large range in the depth to the slab, from Seguam island, with among the shallowest depths to the slab worldwide (~65 km, [1]) to Bogoslof island, behind the main volcanic front and twice the depth to the slab (~130 km). Here we combine thermal models tuned to Aleutian subduction parameters [after 2] with petrological estimates of the T and P of mantle-melt equilibration, using a major element geothermometer [3] and estimates of H2O and fO2 from olivine-hosted melt inclusion measurements [4] for basaltic magmas from 6 volcanoes in the central Aleutians (Korovin, Seguam, Bogoslof, Pakushin, Akutan, Shishaldin). We find mantle-melt equilibration conditions to vary systematically as a function of the depth to the slab, from 30 km and 1220°C (for Seguam) to 60 km and 1300°C (for Bogoslof). Such shallow depths, which extend up to the Moho, define a region perched well above the hot core of the mantle wedge predicted from thermal models, even considering the shallow depths of slab-mantle coupling (< 60 km) required to supply hot mantle beneath Seguam. Thus, even though the greatest melt production will occur in the hot core of the wedge (50-100 km depth), melts apparently ascend and re-equilibrate in the shallowest mantle. Volcanoes that overlie the greatest depth to the slab, and lie furthest from the wedge corner, stall at greater depths (~60 km), at the base of the conductive upper plate (i.e., lithosphere). The conductive lid and isotherms shallow toward the wedge corner. This leads to shallower depths of melt equilibration at shallower depths to the slab. A second effect is infiltration of melt into the thinning lithosphere, likely due to the increase in strain-rate toward the wedge corner, which favors melt segregation, migration, and shallow equilibration [5]. Such a process is developed most beneath Seguam, where melts collect at the Moho (~ 30km), but are still > 1200°C. Such equilibration depths in the uppermost mantle (30-60 km) and temperatures typical of the base of the conductive lid appear to characterize most modeled primary arc magmas [6], and point to a final re-setting point in the mantle that controls the composition of bulk arc crust. [1] Syracuse & Abers, 2006, G3. [2] Syracuse, van Keken, Abers, (2010) PEPI. [3] Lee, Luffi, Plank, Dalton, Leeman (2009) EPSL. [4] Zimmer et al. (2010) J.Pet. [5] Holzman & Kendall (2010). [6] Ruscitto et al. (2012) G3.

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

NASA Astrophysics Data System (ADS)

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 groundwater samples collected in proximity to structures that transmit thermal fluids, suggesting the brine may be thermal in nature. On the western side of the valley at the Lake City mud volcano, the deep brine-meteoric water mixture subsequently boils in the shallow subsurface, precipitates calcite, and re-equilibrates at about 130 °C. On the eastern side of the valley, meteoric fluid mixes to a greater extent with the deep brine, cools conductively without boiling, and the composition is modified as dissolved elements are sequestered by secondary minerals that form along the cooling and outflow path at temperatures <130 °C. Re-equilibration of geothermal fluids at lower temperatures during outflow explains why subsurface temperature estimates based on classical geothermometry methods are highly variable, and fail to agree with temperature estimates based on dissolved sulfate-oxygen isotopes and results of classical and multicomponent geothermometry applied to reconstructed deep well fluids. The proposed model is compatible with the idea suggested by others that thermal fluids on the western and eastern side of the valley have a common source, and supports the hypothesis that low temperature re-equilibration during west to east flow is the major control on hot spring fluid compositions, rather than dilution, evaporation, or differences in rock type.

Detailed thermal fingerprinting of obduction-related processes: insights from Northern New Caledonia

NASA Astrophysics Data System (ADS)

Vitale Brovarone, A.; Agard, P.; Monié, P.; Chauvet, A.

2012-04-01

Northern New Caledonia comprises large and continuous units of high-pressure metamorphic rocks formed in response to the Eocene subduction of a continental margin, classically viewed as a northern extension of the Norfolk ridge, below an oceanic island-arc system (well-exposed in southern New Caledonia) [1, 2]. Metamorphic conditions increase gradually towards the east, providing a continuous window on prograde metamorphism from low-grade, lawsonite-bearing assemblages to epidote-bearing eclogite [3, 4, 5]. Unfortunately, available P-T constraints are mostly restricted to metamafics, but are almost completely lacking in metasediments, which represent the dominant lithology in these mainly continental-derived units. This is due both to the lack of diagnostic mineral assemblages in the metasedimentary lower grade units and to the intense late retrogression affecting the higher-grade metasediments. We herein present an extensive thermometric dataset (encompassing the area from Hienghene to the south and from Koumac to Pouébo) obtained via Raman Spectroscopy of Carbonaceous Material (RSCM), which provides quantitative estimates of the peak metamorphic temperature of CM-bearing metasediments in the range ~200-650°C [6, 7]. Metamorphic conditions vary from about 200 °C in the lower-grade units and progressively increase toward the east to about 550 °C in the eclogite facies unit. Sharp metamorphic gaps are nevertheless found across some major tectonic boundaries (such as the Gendarmerie fault zone). Importantly, the main metamorphic units defined by means of our dataset do not always match with previous studies. This dataset also provides useful insights on the architecture of the high-pressure belt in Northern New Caledonia, where structures are poorly exposed due to thick vegetation. [1] Cluzel, D., Aitchison, J.C., Picard, C., 2001. Tectonic accretion and underplating of mafic terranes in the Late Eocene intraoceanic forearc of New Caledonia (Southwest Pacific): geodynamic implications. Tectonophysics 340 (1-2), 23-59. [2] Ulrich, M., Picard C., Guillot S., Chauvel C., Cluzel D., Meffre S. (2010) The New Caledonia Ophiolite : multiple Stage of melting and refertilisation process as indicators of ridge to subduction formation. Lithos. doi 10.1016/j.lithos.2009.12.011. [3] Brothers, R. N. & Blake, M. C., 1972. Tertiary plate tectonics and high-pressure metamorphism in New Caledonia. Tectonophysics, 17, 359-391. [4] Fitzherbert, J. A., Clarke, G. L. & Powell, R., 2003. Lawsonite- omphacite bearing metabasites of the Pam Peninsula, NE New Caledonia: Evidence for disrupted blueschist to eclogite facies conditions. Journal of Petrology, 44, 1805-1831. [5] Spandler, C., & Hermann, J., 2006. High-pressure veins in eclogite from New Caledonia and their significance for fluid migration in subduction zones. Lithos, 89 (1-2). pp. 135-153. ISSN 1872-6143 [6] Beyssac, O., Goffé, B., Chopin, C. & Rouzaud, J.N., 2002. Raman spectra of carbonaceous material in metasediments: a new geothermometer. J. Metamorph. Geol., 20, 859-871. [7] Lahfid, A., Beyssac, O., Deville, E., Negro, F., Chopin, C. & Goffé, B., 2010. Evolution of the Raman spectrum of carbonaceous material in low-grade metasediments of the Glarus Alps (Switzerland). Terra Nova, 22: 354-360. doi: 10.1111/j.1365-3121.2010.00956.x

Goechemical and Hydrogeochemical Properties of Cappadocia Geothermal Province

NASA Astrophysics Data System (ADS)

Furkan Sener, Mehmet; Sener, Mehmet; Uysal, Tonguc

2016-04-01

In order to determine the geothermal resource potential of Niǧde, Nevşehir and Aksaray provinces in Central Anatolian Volcanic Province (CAVP), geothermal fluids, surface water, and alteration rock samples from the Cappadocia volcanic zone in Turkey were investigated for their geochemical and stable isotopic characteristics in light of published geological and tectonic studies. Accordingly, the Cappadocia Geothermal Province (CGP) has two different geothermal systems located along tectonic zones including five active and two potential geothermal fields, which are located between Tuzgölü Fault Zone and Keçiboyduran-Melendiz Fault and north of Keçiboyduran-Melendiz Fault. Based on water chemistry and isotope compositions, samples from the first area are characterized by Ca-Mg-HCO3 ve Ca-HCO3 type mineral poor waters and Ca-Na-SO4 and Ca-Mg-SO4 type for the cold waters and the hot waters, respectively, whereas hot waters from the second area are Na-Cl-HCO3 and Ca-Na-HCO3 type mineral poor waters. According to δ18O and δ2H isotope studies, the geothermal waters are fed from meteoric waters. Results of silica geothermometer indicate that the reservoir temperature of Dertalan, Melendiz Mount, Keçiboyduran Mount, Hasan Mount (Keçikalesi), Ziga, Acıgöl, and Derinkuyu geothermal waters are 150-173 oC, 88-117 oC, 91-120 oC, 94-122 oC, 131-156 oC, 157-179 oC; 152-174 oC and 102-130 oC, respectively. The REE composition of geothermal fluids, surface water, and mineral precipitates indicate that temperature has a strong effect on REE fractionation of the sampled fluids. Eu- and Ce- anomalies (Eu/Eu*, Ce/Ce*) are visible in several samples, which are related to the inheritance from the host reservoir rocks and redox-controlled fractionation of these elements during water-rock interactions. REE and Yttrium geochemistry results of altered rock samples and water samples, which were taken from same locations exhibited quite similar features in each system. Hence, it was conclude that the same hydrothermal fluid in geothermal system was reached to the surface and interacted with the surface rocks. Our conceptual geothermal model for Cappadocia Geothermal Province based on our geochemical and hydrogeochemical data in combination with geological and geophysical information suggest that the geothermal resources in this region are controlled by primary (active fault) and secondary (buried fault) tectonic belts. Further, our geochemical data indicate the Paleozoic-Mesozoic marble and gneiss being the reservoir rocks. Geogradient and impending heat fluxes to the surface with a possible crustal thinning, which was developed after regional tectonic activities during the Late Pliocene-Quaternary period, constitutes the heat sources. In addition, our study suggest that the Quaternary tuff and ignimbrites of Cappadocia Volcanics represent the seal rock of the geothermal system. In conclusion this study provide evidence for a significant geothermal potential in the Cappadocia region with well-defined seal rocks. However, further studies are needed to resolve the geothermal fluid source problem. Keywords: Cappadocia, geothermal systems, geochemistry, rare earth elements, hydrogeochemistry, hydrothermal alteration.

Pressure-temperature-fluid evolution of the Mongolian Altai in the Central Asian Orogenic Belt: evidence from mineral equilibrium modeling and fluid inclusion studies on amphibolite-facies rocks from western Mongolia

NASA Astrophysics Data System (ADS)

Zorigtkhuu, O.-E.

2012-04-01

The Central Asian Orogenic Belt (CAOB), also known as Altaids, located between the Archean Siberian Craton to the north and the Tarim and North China Cratons to the south, is regarded as one of the largest accretionary and collisional orogen in the world. Detailed petrological studies on the CAOB therefore provide useful information of pressure-temperature (P-T) history of the orogeny as well as the tectonic evolution of East Asia. This study reports detailed petrological data, particularly the results of phase equilibrium modeling and fluid inclusion analysis, of pelitic schists and amphibolites from Bodonch area, southwestern Mongolia, which occupies a significant part of the Paleozoic history of the Altai Orogen in the southwestern margin of the CAOB, and discuss pressure-temperature-fluid evolution of the area. The dominant mineral assemblages of pelitic schist in Bodonch area are garnet + kyanite + staurolite + biotite + plagioclase, garnet + biotite + staurolite + cordierite, and garnet + biotite + sillimanite + plagioclase with quartz and ilmenite, while amphibolite contains calcic amphibole + quartz + plagioclase + garnet + ilmenite assemblage. Application of conventional garnet-biotite and garnet-cordierite geothermometers as well as GASP geobarometer gave metamorphic conditions of 615-635°C/8.2-8.9 kbar from kyanite-bearing pelitic schist samples. Slightly higher P-T condition of 640-690°C/6.3-10.7 kbar was obtained by mineral equilibrium modeling of garnet-kyanite-staurolite and garnet-staurolite-cordierite assemblages using Theriak-Domino software. The calculation was made in the system Na2O-CaO-K2O-FeO-MgO-Al2O3-SiO2-H2O (NCKFMASH). We constructed a clockwise P-T path staring from high-pressure amphibolite facies condition within the stability field of kyanite (approximately 650°C/9 kbar) possibly through the stability field of sillimanite by post-peak decompressional cooling. Our petrographical observations of fluid inclusions in pelitic schists identified primary, secondary and pseudosecondary fluid inclusions trapped in quartz grains. The melting temperatures of all the categories of inclusions lie in the narrow range of -57.5 to-56.6°C, close to the triple point of pure CO2. Homogenization of fluids occurs into liquid phase at temperature between -33.3 to +19.4 °C, which convert into densities in the range of 0.78 to 1.09 g/cm3. The estimated CO2 isochores for primary and pseudosecondary high-density inclusions is broadly consistent with the peak metamorphic condition of the studied area. The results, together with the primary and pseudosecondary nature of the inclusions, indicate CO2 was the dominant fluid component during the peak amphibolite-facies metamorphism of the study area. The common occurrences of carbonates and graphite in the study area suggest the origin of CO2 either by oxidation of organic carbon or devolatilization of carbonates in the protolith sedimentary rocks. Key words: P-T condition; geothermobarometry; mineral equilibrium modeling; fluid inclusion; Altai Orogeny; Central Asian Orogenic Belt; Mongolia

Mineralogy, alteration patterns, geochemistry, and fluid properties of the Ag-Au epithermal deposit Nová Baňa, Slovakia

NASA Astrophysics Data System (ADS)

Majzlan, Juraj; Berkh, Khulan; Kiefer, Stefan; Koděra, Peter; Fallick, Anthony E.; Chovan, Martin; Bakos, František; Biroň, Adrián; Ferenc, Štefan; Lexa, Jaroslav

2018-02-01

In this contribution, we report new data on mineralogy, alteration patterns, geochemistry, fluid properties and source of fluids for the deposit Nová Baňa, one of the smaller epithermal deposits in the Middle Miocene Štiavnica andesite stratovolcano (Western Carpathians, Slovakia). Ore veins and the associated rocks were studied in samples from outcrops and old mines, grab samples, and bore holes from the central part of the deposit (ore structures Althandel, Jozef, Jakub, Vavrinec), northern part (Freischurf), SE part (Gupňa) and SW part (Šibeničný vrch). Pervasive hydrothermal alteration transformed the rock-forming minerals into a mixture of adularia and fine-grained quartz, with lesser amount of pyrite, Ti oxides and Fe oxides. This assemblage was further altered to omnipresent interstratified illite/smectite that was used in this study as a geothermometer, corroborating the results from the fluid inclusion work. Ore minerals comprise predominantly pyrite, sphalerite, galena but all sulfides are relatively sparse in the samples studied. Minerals of precious metals are electrum, Ag-tetrahedrite, acanthite, members of the polybasite-pearceite and pyrargyrite-proustite solid solution, and rare miargyrite, Hg-Ag tetrahedrite, and diaphorite. In the central part, we have found also some stibnite. In the SE part of the deposit, acanthite, uytenbogaardtite, and petrovskaite occur and seem to be related to supergene enrichment of the ores. In bulk ore samples, Zn usually dominates over Pb and Cu. The average Ag:Au ratio for the entire deposit is 64:1. The concentrations of precious metals in the grab samples reach maxima of 50 ppm Au and 570 ppm Ag in the SE part and 116 ppm Au and 1110 ppm Ag in the central part of the deposit. Fluid inclusions show signs of trapping of a heterogeneous fluid. In the central, northern and SE parts of the deposit, homogenization temperatures of 190-260 °C and consistently low salinities of <5 wt% NaCl eq were recorded. In the SW part, primary fluid inclusions gave homogenization temperatures of 160-180 °C and similar low salinities. The secondary inclusions, however, show salinities up to 24 wt% NaCl eq., interpreted as fluid boiling almost to dryness. Isotopic composition of quartz and clay minerals is recalculated to fluid composition of -5.6 to -0.6 ‰ δ18Ofluid and -80 to -36 ‰ δDfluid, indicating mixed character of hydrothermal fluids falling between the compositions of magmatic and meteoric waters, with predominance of meteoric waters. Assuming hydrostatic pressure in the fluids, the measured data suggest paleodepths of ore formation of 50-170 m in the SW part of the ore deposit, 130-420 m in the SE and N parts, and a range of 120-470 m for the central part. These observations, comparison with other epithermal deposits in the Central Slovak volcanic field, and additional data from published literature show that Nová Baňa is a low- to intermediate sulfidation epithermal deposit, genetically associated to late rhyolitic volcanic activity in this area.

Carbon isotope exchange between CO2 and CH4 in hydrothermal fluids from the Tuscan-Roman and Campanian degassing systems (central-southern Italy)

NASA Astrophysics Data System (ADS)

Tassi, F.; Fiebig, J.; Nocentini, M.; Vaselli, O.

2010-12-01

The carbon isotope composition in CO2 and CH4 are commonly used as exploration tools and diagnostic indicators to investigate the origin of endogenous gases. At temperature <200 °C both proportions and isotope ratios of these two gases are considered to be largely controlled by processes (i.e. bacterial activity, thermal hydrolysis, and cracking of organic matter) that are mainly dictated by kinetics. Recent investigations on abiogenic generation of CH4 suggest that at temperatures as low as 100 °C, CH4 production from CO2 has halftimes in the order of 1 year. The present work is based on the d13C-CO2 and d13C-CH4 values of more than 83 gas discharges from the Tuscan-Roman and Campanian degassing systems (central-southern Italy). The main aims are to i) investigate the processes regulating the chemical and isotopic compositions of CO2 and CH4 and ii) verify the use of the CO2-CH4 carbon isotopic equilibrium for evaluating the temperature of deep hydrothermal reservoirs. Our results show that the d13C-CH4 values, with few exceptions related to local production of biogenic CH4 at shallow depth, are > -40 ‰ V-PDB. The most intriguing feature of the measured d13C-CH4 values is that they progressively decrease from the peri-Tyrrhenian area, where productive geothermal systems and active volcanoes are located, to East, i.e. approaching the CH4-rich reservoirs that mark the Adriatic side of the Italian peninsula. The d13C-CO2 values are substantially spanning from a thermometamorphic to a mantle degassing CO2 and do not show any preferential spatial distribution. Secondary carbon isotope fractionation caused by interaction with relatively shallow aquifers may contribute to the scatter of d13C-CO2 values, considering the high solubility of CO2 in liquid water. However, the CO2-CH4 isotopic compositions of fluids from the high temperature geothermal systems characterizing the Tyrrhenian coast of central-southern Italy, i.e. Larderello, Mt. Amiata, Manziana and Phlegrean Fields, provide apparent equilibrium temperatures in the range of those directly measured in production wells and/or estimated on the basis of the CH4-CO2 chemical geothermometer. These results are consistent with the fact that the carbon isotopic equilibrium in the CO2-CH4 system has to be preceded by that of the chemical exchange because the latter has a kinetic rate 400 times faster than the isotopic partitioning. The observed agreement between measured and/or inferred aquifer temperatures with apparent carbon isotopic equilibration supports recent findings that CO2 and CH4 can attain carbon isotopic equilibrium in high-enthalpy hydrothermal systems. The d13C-CH4 values of gas discharges located eastward, toward the Appennine sedimentary chain, are likely produced by mixing of high temperature fluids from the geothermal areas and a relatively cold deep aquifer characterized by biogenic CH4: The higher distance from the geothermal-volcanic systems, the higher fraction of low temperature fluids.

Archaean and Palaeoproterozoic metamorphic events in the Orekhov-Pavlograd compressional zone, Ukrainian Shield

NASA Astrophysics Data System (ADS)

Yurchenko, A. V.

2012-04-01

The Orekhov-Pavlograd zone (OPZ) is located between the Mesoarchaean-Neoarchaean Middle Dnieper Province and the Mesoarchaean-Palaeoproterozoic Azov Province in the eastern Ukrainian Shield. The OPZ consists of Archaean and Palaeoproterozoic high-grade metamorphic rocks. According U-Pb isotope analyses Archaean methaigneous rocks have age of 3.5-3.3 Ga, and latest AR events dated form both individual grains and metamorphic rims in the tonalite and the granitic vein occurred at about 2.88 Ga ego. Paleoproterozoic zircons from a hornblende granulite have a concordia age of 2.08 Ga [1]. P-T conditions of the 3.5-3.3 Ga processes calculated from the Ti content in zircon are of 730-760°C. Metamorphic event dated as 2.88 Ga is more preserved and detected in some amphibolites after mafic dykes. According to different methods of hornblende-plagioclase geothermometry along with Al- and Ti-geobarometry of hornblende, the amphibolites have formed at temperature of 735-749 °C and pressure of 5.2 to 7.8 kbar. P-T conditions of Paleoproterozoic metamorphic processes have been calculated for a Paleoproterozoic high-Al paragneiss and mafic rocks. On the base of the computer software THERIAK-DOMINO [2], near-isothermal decompression from ca. 8.5 to 6.0 kbar at 650 °C and then to 5.8 kbar at 740 °C has been determined for small irregular garnet grains (grs 4-7% and XMg 0.36-0.37) associated with the same biotite and plagioclase. P-T conditions obtained by means of the P-T pseudosection calculation are identical within errors to those defined by the Grt + Bt + Pl + Ozt geothermometer by [3] and the geobarometer by [4], T = 675 °C and P = 5.6 kbar. Temperature and pressure calculated for assemblage Grt-Pl-Opx-Amph-Ilm-Ru (mafic rock) by using the TWEEQU method shows: 1) high values of pressure and temperature (ca. 7 kbar and 800 °C) are linked with the first metamorphic event with Opx-Cpx assemblage, 2) moderate values (ca. 5 kbar and ca. 600 °C) are referred to the second metamorphic event when amphibole was crystallized instead of orthopyroxene. The latest metamorphic reworking took place at P = 3.3-4 kbar and T = ca. 600 °C. The resulting Paleoproterozoic P-T-t path suggests a clockwise P-T evolution of the OPZ area. Preferences: 1. S.B.Lobach-Zhuchenko, Yu.S.Egorova, A.V.Yurchenko, V.V.Balagansky, G.V.Artemenko, V.P.Chekulaev, N.A.Arestova, 2009. Mineralogical Journal (Kiev), 31 (1): 3-10. 2. de Capitani, C., 2005. THERIAK - DOMINO User's Guide, Version 1402005, http://titan. minpet.unibas.ch/minpet/theriak/theruser.html (04/2007). 3. Ferry, J.M., Spear, F.S., 1978. Experimental calibration of the partitioning of Fe and Mg between biotite and garnet. Contrib. Mineral. Petrol. 66, 113-117. 4. Koziol, A.M., Newton, R.C., 1989. Grossular activity-composition relationship in ternary garnets determined by reversed displaced-equilibrium experiments. Contrib. Mineral. Petrol. 103, 423-433.

Geochemical signature of permanent and ephemeral thermal springs in Val di Cornia, Central Italy

NASA Astrophysics Data System (ADS)

Pierotti, Lisa; Pennisi, Maddalena; Muti, Antonio; Gherardi, Fabrizio

2014-05-01

In the Val di Cornia area, several permanent thermal springs outflow. They belong to the hydrothermal system of Campiglia Marittima and have been exploited since longtime for the therapeutic properties of the discharged waters. With an average outflow of 250 L/sec, Calidario (36.3±0.2° C) is the most important permanent spring of the area. Periodically, i.e. about every 10 years, a number of ephemeral thermo-mineral springs in Bagnarello (46±0.2° C) and Monte Peloso (42.2±0.3° C) area, spontaneously reactivate over short time periods (several weeks to few months), with a maximum discharge of 150±20 L/sec. This phenomenon is generally induced by intensive rainfall events. In this contribution, we present new geochemical analyses of waters discharged from Calidario and the ephemeral springs reactivated at the beginning of 2001 and at the end of 2010. These new data are then compared to previous analyses to investigate geochemical variations over a 30-years period. Both ephemeral and permanent thermal springs have Ca-SO4 geochemical signature, typical of groundwaters circulating through the carbonate-evaporitic complexes of the Tuscan Nappe (Mesozoic age). Clear salinity trends are identified, with TDS increasing from Calidario to Monte Peloso and Bagnarello springs, up to a maximum of about 3000 ppm. Chemical speciation indicates that most of the thermal waters are close to saturation with respect to fluorite and gypsum/anhydrite, with solute geothermometers indicating possible equilibrium temperature of 50-55° C for Monte Peloso and Bagnarello waters, respectively. Higher temperatures, up to 75° C, were inferred by assuming equilibrium at depth with the aluminosilicates of the regional Basement (phyllitic formations of Paleozoic age), below the evaporites of the Tuscan Nappe (Triassic age). With δ18O and δ2H values of -6.4 (±0.2)o and -38.9 (±2.9)o respectively, the ephemeral springs have a steady stable isotope composition, comparable to permanent thermal springs. Based on these data, the main recharge area has been hypothesized in correspondence of outcropping carbonate formations in the hilly region NE of the area under study. The lack of tritium (3H) at Bagnarello suggests the existence of long underground residence times for the hydrothermal component, whereas the presence of measurable amounts of tritium at Calidario indicate the contribution of rapidly infiltrating meteoric waters. The 87Sr/86Sr ratio of ephemeral and permanent thermal springs (below 0.70804), significantly lower than local Ca-HCO3 groundwaters (0.70889), indicates a prolonged interaction with Mesozoic carbonate and evaporitic formations (0.70789). The δ34S-SO4 signature (+15.4o) mirrors the isotopic composition of local evaporites, reinforcing on the hypothesis of extensive thermal circulation through the Tuscan Nappe. Overall, the geochemical signature of the thermal springs of the Campiglia Marittima hydrothermal spring appears stable over the period 1984-present. Geochemical data support a regional groundwater circulation scheme where thermal waters move along a preferential NE-SW direction, flow at different depths within Mesozoic carbonate and evaporite formations, and emerge in correspondence of main faults.

Low grade metamorphism fluid circulation in a sedimentary environment thrust fault zone: properties and modeling

NASA Astrophysics Data System (ADS)

Trincal, Vincent; Lacroix, Brice; Buatier, Martine D.; Charpentier, Delphine; Labaume, Pierre; Lahfid, Abdeltif

2014-05-01

In fold-and-thrust belts, shortening is mainly accommodated by thrust faults that can constitute preferential pathways for fluid circulation. The present study focuses on the Pic de Port Vieux thrust, a second-order thrust related to major Gavarnie thrust in the Axial Zone of the Pyrenees. The fault juxtaposes lower Triassic red siltstones and sandstones in the hanging-wall and Upper Cretaceous limestone in the footwall. A dense network of synkinematic quartz-chlorite veins is present in outcrop and allows to unravel the nature of the fluid that circulated in the fault zone. The hanging wall part of fault zone comprises a core which consists of intensely foliated phyllonite; the green color of this shear zone is related to the presence of abundant newly-formed chlorite. Above, the damage zone consists of red pelites and sandstones. Both domains feature kinematic markers like S-C type shear structures associated with shear and extension quartz-chlorite veins and indicate a top to the south displacement. In the footwall, the limestone display increasing mylonitization and marmorization when getting close to the contact. In order to investigate the mineralogical and geochemical changes induced by deformation and subsequent fluid flow, sampling was conducted along a complete transect of the fault zone, from the footwall limestone to the red pelites of the hanging wall. In the footwall limestone, stable isotope and Raman spectroscopy analyzes were performed. The strain gradient is strongly correlated with a high decrease in δ18OV PDB values (from -5.5 to -14) when approaching the thrust (i.e. passing from limestone to marble) while the deformation temperatures estimated with Raman spectroscopy on carbon remain constant around 300° C. These results suggest that deformation is associated to a dynamic calcite recrystallization of carbonate in a fluid-open system. In the hanging wall, SEM observations, bulk chemical XRF analyses and mineral quantification from XRD analyses were conducted in order to compare the green phyllonites from the fault core zone with the red pelites from the damage zone. Quartz, muscovite 2M1, chlorite (clinochlore), calcite and rutile are present in all samples. Hematite occurs in the damage zone but is absent in the core zone. Synkinematic chlorites are abundant in the core and damage zones and are mainly located in veins, sometimes in association with quartz. The temperature of formation of these newly-formed chlorites is 300-350° C according to Inoue (2009) geothermometer. Mössbauer spectroscopic analyses were performed on bulk rock samples. In the damage zone, Fe3+/Fetotal vary between 0.7 and 0.8, whereas in the core zone Fe3+/Fetotal is about 0.35. This decrease in Fe3+ from the damage zone to the core zone can be related to the dissolution of hematite. In contrast, Fe3+/Fetotal in phyllosilicates is clearly related to the chlorite content relative to mica, as Fe2+ increases with chlorite content. All these data allow us to propose a model of fluid circulation in relation with the Pic de Port Vieux thrust activity. The origin of the fluid, its interactions with host-rock and the consequences on fault zone mineralizations will be discussed. Inoue, A., Meunier, A., Patrier-Mas, P., Rigault, C., Beaufort, D., Vieillard, P., 2009. Application of chemical geothermometry to low-temperature trioctahedral chlorites. Clay Clay Min. 57, 371-382.

Volatile budget of the Nornahraun eruption of the Bárðarbunga system, Iceland

NASA Astrophysics Data System (ADS)

Bali, Eniko; Sigmarsson, Olgeir; Jakobsson, Sigurdur; Gunnarsson, Haraldur

2015-04-01

Following two weeks of an intensive earthquake swarm coupled with approximately 60 cm E-W extension across the volcanic zone north of Vatnajökull glacier, a fissure eruption started on 29th of August 2014 in the Bárðarbunga volcanic system. The continuing eruption produced lava fountains and a lava field associated with minor tephra fallout. The lava is an almost aphyric, olivine tholeiite, containing 1 to 3 vol% of plagioclase and minor olivine and clinopyroxene phenocrysts (Gudfinnsson et al., this session). Fast cooled tephra was collected on 31st of August and 4th and 8th of September from the vicinity of the fissure. Phenocryst phases as well as groundmass glass have been handpicked and doubly polished and analysed for H2O and CO2 with FTIR-spectroscopy. The phenocrysts contain glassy silicate melt inclusions with or without a fluid bubble and some phenocrysts also contain free fluid inclusions. The fluid phase and the individual fluid inclusions were analysed by Raman Spectroscopy and the abundance of other volatiles (S, F, Cl) has been determined by electron microprobe from exposed inclusions and groundmass glass. The H2O content of melt inclusions varies between 0.1 and 0.5 wt% whereas the CO2 contents are between 900 ppm and detection limit indicating various entrapment conditions of the melt inclusions after fluid saturation. S contents in melt inclusions are as high as 1600 ppm whereas F and Cl contents in the same inclusions are low (~300 and ~90 ppm, respectively). Groundmass glass contains 0.1 wt% of H2O, ~400 ppm S and no CO2. F and Cl in groundmass glass is similar to those measured in the melt inclusions. Based on the Raman analyses individual fluid inclusions are pure CO2. The highest determined CO2 density was 0.642 g/cm3 (using the method by Kawakami et al., 2003). At a temperature of 1180 °C, which is assumed to be the equilibrium temperature of the basalt based on various geothermometers (Haddadi et al., this session), this CO2 density corresponds to an approximately 3 kbar entrapment pressure (~9 km entrapment depth). This means that the basalt became CO2 saturated at lower to mid-crustal levels. CO2 solubility at 1180 °C and 3 kbars pressure is at least 1500 ppm in basalt (calculated by Volatilecalc, Newman and Lowernstern, 2002). Consequently all melt inclusions analysed so far must have been trapped from partially degassed basalt but before (and deeper) than the onset of H2O and S degassing. Taking into account the current estimation of extrusion rate the estimated CO2 output by this eruption is 500 kg/s whereas SO2 output is on the order of 1000 kg/s. References: Gudfinnsson et al., this session: Petrography and petrology of the new fissure eruption of the Barðarbunga system, Iceland. Haddadi et al., this session: Determining intensive parameters through clinopyroxene-liquid equilibrium in Grímsvötn 2011 and Bárðarbunga 2014 basalts. Kawakami et al., (2003): Micro-Raman densimeter for CO2 inclusions in mantle-derived minerals. Appl. Spectrosc. 57, 1333-1339. Newman, S. Lowernstern, J.B. (2002): VolatileCalc: a silicate melt-H2O-CO2 solution model written in Visual Basic for excel. Comp Geosci, 28, 597-604.

Geochemistry and metamorphism of the Paleozoic metasedimentary basement of the Sierra Madre Oriental, NE Mexico. Possible paths from their depositional environment?

NASA Astrophysics Data System (ADS)

Torres Sanchez, Sonia Alejandra; Augustsson, Carita; Alonso Ramirez Fernandez, Juan; Rafael Barboza Gudiño, Jose; Jenchen, Uwe; Abratis, Michael

2013-04-01

We present depositional conditions and possible protholits for Late Paleozoic metasediment in Mexico that were related to the Laurentia-Gondwana collision in Carboniferous time, during Pangea amalgamation. The study aims to reconstruct the depositional and metamorphic evolution of the Granjeno Schist in northeastern Mexico to get a better control on the timing of subduction and collision processes involving the two supercontinents. Remnants of the Mexican Paleozoic continental configuration are present in the Granjeno Schist, the metamorphic basement of the Sierra Madre Oriental in northeastern Mexico. We apply field mapping, petrographic investigations, whole-rock and mineral chemical analysis, as well as U-Pb zircon dating of both metasedimentary and metavolcanic rocks. Field work and petrographic analysis reveal that the Granjeno Schist comprises intercalations of metamorphic rocks with both sedimentary (psammite, pelite, turbidite, conglomerate, black shale) and volcanic (tuff, lava flows, pillow lava and ultramafic bodies) protoliths. The chlorite geothermometer and the presence of phengite in the metasedimentary units as well as U-Pb zircon ages on metapsammite indicate that the Granjeno Schist was metamorphosed under sub-greenschist to greenschist facies with temperatures ranging from 250-345°C during the Carboniferous time (330±30 Ma). The geochemical composition of the metasedimentary rocks is in accordance with iron shale, wacke and quartz arenite protoliths. Some of the variations can be explained by the grain sizes (e. g., 69-74% and 78-96% SiO2 and 10-15% and 3-9% Al2O3 in metapelite and metapsammite, respectively). Our data suggest that the Granjeno Schist metasedimentary units represent a wide variety of clastic sediments derived from mixed felsic basic sources compositions (e. g., Ti/Nb 200-400). Furthermore, the trace element characteristics point to a continental island arc or active continental margin setting due to e. g., Th/Sc and Zr/Sc ratios of 5-8 and 0.3-0.5, respectively, both for metapelite and metapsammite. The metavolcanic rocks are associated with ocean-island basalt (OIB) or mid-ocean ridge basalts (MORB) due to the immobile trace element ratios Zr/Nb and Y/Nb in the ranges 4.91-8.06 and 0.74-1 for the IOB and >9.2 and >1.25 for the MORB, respectively. Detrital zircon ages for three metapsammites reveal that the major sources mainly are Grenvillian (1250-920 Ma) rocks. Such rocks can be found in the ca. 1 Ga Oaxaquia Complex in NE Mexico (Novillo Gneiss). Hence, short transport can be assumed. Maximum depositional ages are Neoproterozoic, Silurian and Devonian. They indicate that the volcanosedimentary deposition probably took place during Devonian time. Based on our results we suggest a plate-tectonic frame for Oaxaquia which is a modification of accepted models. Most models suggest that Oaxaquia was situated between Laurentia and Gondwana during collision in Carboniferous time. The zircon data indicate that the Granjeno Schist was deposited before the collision of Laurentia and Gondwana. The presence of ocean basalt floor, lava flows and serpentinite lenses intercalated with tuff and active continental margin sedimentary rocks necessitates a near-continental environment, such as a back-arc basin. Hence, we present the first evidence of a subduction zone predating the collision of Laurentia and Gondwana.

A new garnet-orthopyroxene thermometer developed: method, results and applications

NASA Astrophysics Data System (ADS)

Olivotos, Spyros-Christos; Kostopoulos, Dimitrios

2014-05-01

The Fe-Mg exchange reaction between garnet and orthopyroxene is a robust geothermometer that has extensively been used to retrieve metamorphic temperatures from granulitic and peridotitic/pyroxenitic lithologies with important implications on the thermal state of the continental lithosphere. More than 800 experimental mineral pairs from both simple and complex systems were gleaned from the literature covering the P-T range 0.5-15 GPa / 800-1800°C. Grt was treated as a senary (Py, Alm, Grs, Sps, Kno and Uv), whereas Opx as a septenary (En, Fs, Di, Hd, FeTs, MgTs and MgCrTs) solid solution. For Opx, Al in the M1 site was calculated following Carswell (1991) and Fe/Mg equipartitioning between sites was assumed. A mixing on sites model was employed to calculate mole fractions of components for both minerals. With regard to the excess free energy of solution and activity coefficients the formalism of Mukhopadhyay et al. (1993) was adopted treating both minerals as symmetric regular solutions. Calibration was achieved in multiple steps; in each step ΔS was allowed to vary until the standard deviation of the differences between experimental and calculated temperature for all experiments was minimised. The experiment with the largest absolute relative deviation in temperature was then eliminated and the process was repeated. The new thermometer reproduces the experimental data to within 50°C and is independent of P-T-X variations within the bounds of the calibrant data set. Application of our new calibration to metamorphosed crustal and mantle rocks that occur both as massifs and xenoliths in volcanics suggested the following results. Granulite terranes have recorded differences in temperature between peak and re-equilibration conditions in the range 100-340°C, primarily depending on the mechanism and rate of exhumation. Several provinces retain memory of discrete cooling pulses (e.g. Palni Hills, South Harris, Adirondacks, E. Antarctic Belt, Aldan Shield) whereas others are dominated by a single thermal event (Lisof Massif, SW Greenland, Eifel). UHT granulites appear to be more common than previously thought. There are a considerable number of localities in Europe that have recorded temperatures in excess of 950°C (South Harris, Schwarzwald, Pannonian Basin, Sudetes, Rogaland, Massif Central, Iberian Hercynian Belt), with the first four listed peaking over 1000°C. In settings such as South Harris, the model of Schmalholz & Podladchikov (2013) for heat generation within a crustal-scale shear zone is most appealing. Mafic/ultramafic xenoliths from Deccan conform to geotherms with surface heat flow between 60 and 90 mW.m-2 signifying a reduction in lithospheric thickness of the order of 43 km. Similar xenoliths from the Tariat Depression testify to a 20 km thinning beneath Mongolia. Mantle xenoliths from Canadian and Russian kimberlites demonstrate the great diamond potential of the Lac des Gras, Jericho, Udachnaya and Mir pipes but the limited potential of the Somerset Isl. and Obnazhennaya pipes. UHP mantle peridotites from the Dabie-SuLu orogen are characterised by the coldest geotherm identified so far (33mW.m-2) implying a minimum removal of 110 km from the lithospheric keel underneath E. China. References: Carswell, D. A., 1991. Min. Mag. 55, 19-31; Mukhopadhyay, B., et al., 1993. GCA 57, 277-283; Schmalholz, S. M., & Podladchikov, Y. Y., 2013. GRL 40, 1984-1988.

Phenocrysts and megacrysts of olivines from ultramafic lamprophyres of the Chadobets and Il'bokich uplifts, Southwestern Siberia

NASA Astrophysics Data System (ADS)

Smirnova, Maria; Sazonova, Lyudmila; Nosova, Anna; Kargin, Alexey; Shcherbakov, Vasiliy

2017-04-01

The study of composition and zoning of olivines from ultramafic lamprophyres of the SW Siberian craton allowed us to distinguish their main types (phenocrysts and megacrysts) and to estimate the possible P-T conditions of phenocryst crystallization. The studied rocks occur as sills and dikes in the Chadobets and Il'bokich uplifts of the Irkeneeva-Chadobets trough. The ultramafic lamprophyres of these uplifts are spaced around 80 km apart and differ in age by more than 150 Ma. The rocks of the Il'bokich Uplift are dated at Devonian, while the age of the Chadobets Complex is restricted to the Triassic. The episodes of these complexes formation were separated by the large flood basalt event. According to classification (Tappe et al., 2005), the studied rocks are aillikite and damtjernite. Olivine phenocrysts from the rocks of the Il'bokich and Chadobets complexes are represented by sub- and euhedral grains. They are composed of core, transitional zone, and rim. Olivine cores in the aillikites of the Il'bokich Complex are characterized by Mg# 89; CaO - 0.13-0.14 wt %; TiO2 around 0.03 wt %, Al - 200-380 ppm, and Cr - 130-340 ppm. The cores of phenocrysts from the Chadobets lamprophyres have Mg# 85-87, CaO varying within 0.1-0.2 wt %, and TiO2 - 0.02-0.05 wt %. The megacrysts differ from the phenocrysts of these rocks in the lower Mg# 83-84 and CaO - 0.08-0.14 wt % at higher TiO2 - 0.04-0.05 wt %. Al - 100-700 ppm, Cr - 20-65 ppm. The most striking difference between olivines of the two complexes is observed between their Mg#-Ni relations. The cores of olivine phenocrysts from the Il'bokich lamprophyres are characterized by the high Mg number (Mg# = 89) and Ni content (2800-3000 ppm), whereas olivine cores of the Chadobets aillikites have higher contents of Ni (3000-3500 ppm) at lowered (Mg# = 86-88). These characteristics reflect the compositions of their protolith. The temperature was estimated using monomineral olivine thermometer based on the contents of Cr and Al in olivine (De Hooge et al., 2010). This geothermometer was calibrated for a wide compositional range, including kimberlites, and correspondingly, may be used for alkaline-ultrabasic lamprophyres. At pressures above 4 GPa, olivine phenocrysts fall in the field of olivine-kimberlite melt equilibrium (Girnis et al., 1995). The Il'bokich olivine phenocrysts were formed at higher temperature than the Chadobets phenocrysts: from 1240 to 1340oC for the Il'bokich rocks and from 1080 to 1225oC for the Chadobets rocks. In the P-T diagram showing the geotherm of 40 mV/m2, olivines from the Il'bokich and Chadobets lamprophyres lie to the right of the geotherm, which excludes the presence of xenogenic lithospheric mantle olivine in these rocks. De Hoog J.C.M., Gall L., Cornell D.H. 2010. Trace-element geochemistry of mantle olivine and application to mantle petrogenesis and geothermobarometry // Chem. Geol. 270.1: 196-21. Girnis A.V., Brey G.P., Ryabchikov I.D. 1995. Origin of group 1A kimberlites: fluid-saturated melting experiments at 45-55 kbar // EPSL. 134.3: 283-296. Tappe S., Foley S.F., Jenner G.A. et al. 2006. Genesis of Ultramafic Lamprophyres and Carbonatites at Aillik Bay, Labrador: a Consequence of Incipient Lithospheric Thinning beneath the North Atlantic Craton // J. Petrology. 47 (7). 1261-1315.

The clumped isotope geothermometer in soil and paleosol carbonate

NASA Astrophysics Data System (ADS)

Quade, J.; Eiler, J.; Daëron, M.; Achyuthan, H.

2013-03-01

We studied both modern soils and buried paleosols in order to understand the relationship of temperature (T°C(47)) estimated from clumped isotope compositions (Δ47) of soil carbonates to actual surface and burial temperatures. Carbonates from modern soils with differing rainfall seasonality were sampled from Arizona, Nevada, Tibet, Pakistan, and India. T°C(47) obtained from these soils shows that soil carbonate forms in the warmest months of the year, in the late morning to afternoon, and probably in response to intense soil dewatering. T°C(47) obtained from modern soil carbonate ranges from 10.8 to 39.5 °C. On average, T°C(47) exceeds mean annual temperature by 10-15 °C due to summertime bias in soil carbonate formation, and to summertime ground heating by incident solar radiation. Secondary controls on T°C(47) are soil depth and shading. Site mean annual air temperature (MAAT) across a broad range (0-30 °C) of site temperatures is highly correlated with T°C(47) from soils, following the equation: MAAT(°C)=1.20(T°C(47)0)-21.72(r2=0.92) where T°C(47)0 is the effective air temperature at the site estimated from T°C(47). The effective air temperature represents the air temperature required to account for the T°C(47) at each site, after consideration of variations in T°C(47) with soil depth and ground heating. The highly correlated relationship in this equation should now permit mean annual temperature in the past to be reconstructed from T°C(47) in paleosol carbonate, assuming one is studying paleosols that formed in environments generally similar in seasonality and ground cover to our calibration sites. T°C(47)0 decreases systematically with elevation gain in the Himalaya, following the equation: elevation(m)=-229(T°C(47)0)+9300(r2=0.95) Assuming that temperature varied similarly with elevation in the past, this equation can be used to reconstruct paleoelevation from clumped isotope analysis of ancient soil carbonates. We also measured T°C(47) from long sequences of deeply buried (⩽5 km) paleosol carbonate in the Himalayan foreland in order to evaluate potential diagenetic resetting of clumped isotope composition. We found that paleosol carbonate faithfully records plausible soil T°C(47) down to 2.5-4 km burial depth, or ˜90-125 °C. Deeper than this and above this temperature, T°C(47) in paleosol carbonate is reset to temperatures >40 °C. We observe ˜40 °C as the upper limit for T°C(47) in modern soils from soil depths >25 cm, and therefore that T°C(47) >40 °C obtained from ancient soil carbonate indicates substantially warmer climate regimes compared to the present, or non-primary temperatures produced by resetting during diagenesis. If representative, this limits the use of T°C(47) to reconstruct ancient surface temperature to modestly buried (<3-4 km) paleosol carbonates. Despite diagenetic resetting of Δ47 values, δ18O and δ13C values of the same deeply buried paleosol carbonate appear unaltered. We conclude that solid-state reordering or recrystallization of clumping of carbon and oxygen isotopes can occur in the absence of open-system exchange of paleosol carbonate with significant quantities of water or other phases.

Experimental Determination of Fe-Mg Interdiffusion Coefficients in Orthopyroxene Using Pulsed Laser Ablation and Nanoscale Thin Films

NASA Astrophysics Data System (ADS)

Ter Heege, J. H.; Dohmen, R.; Becker, H.; Chakraborty, S.

2006-12-01

Fe-Mg interdiffusion in silicate minerals is of interest in petrological studies for determining the closure temperature of geothermometers and for determining cooling rates from compositional profiles. It is also relevant for studies of the physical properties of silicates, such as rheology or electrical conductivity, because knowledge of its dependence on oxygen fugacity can aid in the understanding of point defect chemistry. Compositionally zoned orthopyroxenes are common in meteorites, mantle rocks, lower crustal rocks and a variety of plutonic and volcanic igneous rocks. However, experimental difficulties have precluded direct determination of Fe-Mg diffusion rates in orthopyroxenes so far and the available information comes from (1) Mg tracer diffusion coefficients obtained from isotope tracer studies using enriched ^{25}MgO films [1], (2) calculations of interdiffusion rates based on the (diffusion-controlled) order-disorder kinetics measured in orthopyroxene [2], and (3) indirect estimates from the comparison of diffusion widths in coexisting garnets and olivines, in which Fe-Mg diffusion rates are relatively well known [e.g., 3]. We have directly measured Fe-Mg interdiffusion coefficients parallel to the [001] direction in two natural orthopyroxene single crystals (approximately En95Fs5 and En90Fs10) using diffusion couples consisting of an olivine thin film (Fo30Fa70, typically 20 - 50 nm thick) deposited under vacuum on pre-heated, polished and oriented pyroxene single crystals using a pulsed laser ablation deposition technique. Samples were annealed for 4 - 337 hours at 800 - 1100 °C under atmospheric pressure in a continuous flow of CO + CO2 to control the oxygen fugacity between 10-16 and 10^{-12} bar within the stability field of pyroxene. Film thickness and compositional profiles were measured using Rutherford backscattering Spectroscopy (RBS) on reference and annealed samples, and Fe concentration depth profiles were extracted from the RBS spectra and fitted numerically. At an oxygen fugacity of 10-16 bar, Fe-Mg interdiffusion coefficients in the Fs richer orthopyroxene vary between 4.10^{-22} m2/s and 2.10^{-20} m2/s for temperatures between 800 and 1000°C. Diffusion coefficients decrease by a factor of ~ 4 with decreasing oxygen fugacity between 10^{-12} and 10-16 bar at 1000 °C. Comparison of our data with other Fe-Mg diffusion data shows that these diffusion coefficients are (1) similar to Mg tracer diffusion coefficients measured in orthopyroxene at somewhat more reducing (e.g. fO2 = 10-16 to 10^{-19} bar) conditions at the same temperatures [1], (2) similar to Mg tracer diffusion in garnets measured at higher pressures of 10 kbar at an oxygen fugacity corresponding to the C-O equilibrium in graphite present systems [4], and (3) slower than Fe-Mg diffusion rates in olivine by a factor of ~10 at the same oxygen fugacities [5]. Further experiments to quantify the dependence on composition, temperature and oxygen fugacity are in progress. References: [1] Schwandt et al. (1998), Contr. Mineral. Petrol. 130: 390-396; [2] Ganguly and Tazzoli (1994), Am. Mineral. 79: 930-937; [3] Smith and Barron (1991), Am. Mineral. 76: 1950-1963; [4] Ganguly et al. (1998), Contr. Mineral. Petrol. 131: 171-180; [5] Chakraborty (1997), J. Geoph. Res. 102: 12317-12331.

Decoding recent mud-volcano activity in the westernmost Mediterranean: Evidence from sediment/porewater data and geochemical modeling

NASA Astrophysics Data System (ADS)

López-Rodríguez, Carmina; Martínez-Ruíz, Francisca; Mogollón, José M.; Comas, Menchu; Nieto, Fernando; Böning, Philipp; Pahnke, Katharina; Sapart, Célia; De Lange, Gert J.

2017-04-01

Recent studies have demonstrated the occurrence of active mud volcanism in the West Alboran Basin. Though most of the mud volcanoes (MVs) discovered in this region are dormant, a few structures evidence active hydrocarbon venting, as Carmen MV. This study focuses on sedimentological and geochemical investigations on one piston core, GP05PC, recovered from the summit of Carmen MV during the Gasalb-Pelagia cruise (2011). Although the full core consists of mud breccia sediments, a dramatic change occurs between enhanced methane concentrations in its lowermost and dissolved SO42- in its uppermost sediments. At the boundary of 150 cm, methane is oxidized and sulphate reduced. In the lowermost interval, the depletion of major elements (i.e., Ca2+ and Mg2+), the enrichment of trace species (i.e., Li+ and B) and the radiogenic 87Sr all point to a deep fluid source. The δ18Opw and δDpw compositions of pore water (5.7‰ and -10‰ VSMOW, respectively) together with the mineralogical results (presence of randomly insterstrafied (R0) illite-smectite minerals (I/S) to more illitic (>50% I) and ordered ones (R1-R3)) indicate smectite to illite transformation at greater depth and support smectite dehydration as the main porewater freshening mechanism. Water formation temperatures calculated through the application of empirical geo-thermometers (K-Na, K-Mg and K-Ca) together with the presence from I/S mixed layers (R3) suggest that fluids were generated at temperatures 100-200°C. This temperature indicates that, under a regional geothermal gradient, the fluid source originates from 8 km depth. From an adjacent borehole it is known that sedimentary units of Early to Middle Miocene age occur at that depth (Jurado and Comas et al., 1992). The δ13Cmethane and δDmethane composition of methane (-59‰ VPDB and -184‰ VSMOW, respectively) of the deepest sample also may be associated to a thermogenic origin. The absence of hemipelagic sediment draping, the distinctive seawater-like pore water composition in the uppermost part of the mud breccia together with the abrupt transition to the interval with typical deep-source fluid composition, all point to a very recent mud and associated gas-expulsion. Such outburst leads to the downward intrusion of seawater coincident with the episode of gas-bubble expulsion. A numerical transport-reaction model has been applied to the distinctively kink-shaped pore water Cl, SO42-CH4, and other profiles in core GP05PC, to derive the very recent timing for this eruption event (López-Rodríguez et al., 2017). References: Jurado, M. J. and Comas, M. C. (1992). Well log interpretation and seismic character of the Cenozoic sequence in the Northern Alboran Sea, Geo-Marine Letters, 12, 129-136. López-Rodríguez, C., Martínez-Ruíz, F., Mogollón, J.M., Comas, M. Nieto, F, Böning P.H., Pahnke, K., Sapart, C. and De Lange, G.J. (2017). Evidence for a 2000 AD +/- 3 yr mud/methane discharge event in the westernmost Mediterranean (based on sediment/pore water data and modelling). Manuscript submitted for publication.

Four magnetite generations in the Precambrian Varena Iron Ore deposit, SE Lithuania, as a result of rock-fluid interactions

NASA Astrophysics Data System (ADS)

Skridlaite, Grazina; Prusinskiene, Sabina; Siliauskas, Laurynas

2017-04-01

Iron ores in Precambrian crystalline basement of the Varena area, SE Lithuania, were discovered during the detail geological-geophysical exploration in 1982-1992. They are covered with 210-500 m thick sediments. The Varena Iron Ore deposit (VIOD) may yield from 71 to 219.6 million tons of iron ore according to different economic evaluations (Marfin, 1996). They were assumed to be of metasomatic and hydrothermal origin, however several other hypotheses explaining the VIOZ origin, e.g. as a layered mafic or carbonatite intrusions were also suggested. Magnetites of the VIOD were thoroughly investigated by the Cameca SX100 microprobe at the Warsaw University and by the Quanta 250 Energy Dispersive Spectroscopy (EDS) at the Nature Research Centre in Vilnius, Lithuania. Four generations of magnetite were distinguished in the studied serpentine-magnetite ores (D8 drilling) and were compared with the earlier studied and reference magnetites. The earliest, spinel inclusion-rich magnetite cores (Mag-1) have the highest trace element contents (in wt%): Si (0.032), Al (0.167-0.248), Mg (0.340-0.405), Ti (0.215-0.254), V (0.090-0.138) etc. They might have formed during an early metamorphism and/or related skarn formation. Voluminous second magnetite (Mag-2) replacing olivine, pyroxenes, spinel and other skarn minerals at c. 540o C (Magnetite-Ilmenite geothermometer) has much lower trace element abundances, probably washed out by hydrothermal fluids. The latest magnetites (Mag-3 and Mag-4) overgrow the earlier ones and occur near or within the sulfide veins (Mag-4). As was observed from microtextures, the Mag-3 and Mag-4 have originated from the late thermal reworking by dissolution-reprecipitation processes. To imply an origin of the studied magnetites, they were compared to the earlier studied magmatic-metamorphic (1058 drilling), presumably skarn (982 drilling) magnetites from the studied area and plotted in the major magnetite ore type fields according to Dupuis and Beaudoin (2011). They have similar trace element abundances as skarn magnetites, e.g. are in general Ti-poor. The Mag-1 is more than twice richer in Mg than the porphyry and Kiruna type iron ores. A slight enrichment in Al, Ti and V because of spinel and ilmenite inclusions may have caused the earliest Mag-1 to resemble the porphyry type ores, while the secondary Mag-2 has Al, Ca and Mn contents as low as the Kiruna type ores. Thus, we can consider that fluid-rock interactions have strongly affected chemical compositions of the studied magnetites. Even though there are no precise age constructions for the metamorphic, metasomatic and hydrothermal iron ore formation process, they likely started later than 1.80 Ga (metamorphism of the host rocks; Bogdanova et al., 2015) and lasted until c. 1.50 Ga, when the rocks were intruded by the within-plate AMCG magmatic bodies. Bogdanova, S., Gorbatschev, R., Skridlaite, G., Soesoo, A., Taran, L., Kurlovich, D., 2015. Precambrian Research, 259, 5-33. Dupuis, C., Beaudoin, G., 2011. Mineral Deposita 46, 319-335. Marfinas, S., 1996. Report on the results of the evaluation of the Varena Iron Ore deposit, 2nd book, Vilnius.

Element migration of pyrites during ductile deformation of the Yuleken porphyry Cu deposit (NW-China)

USGS Publications Warehouse

Hong, Tao; Xu, Xing-Wang; Gao, Jun; Peters, Stephen; Li, Jilei; Cao, Mingjian; Xiang, Peng; Wu, Chu; You, Jun

2017-01-01

The strongly deformed Yuleken porphyry Cu deposit (YPCD) occurs in the Kalaxiangar porphyry Cu belt (KPCB), which occupies the central area of the Central Asian Orogenic Belt (CAOB) between the Sawu’er island arc and the Altay Terrane in northern Xinjiang. The YPCD is one of several typical subduction-related deposits in the KPCB, which has undergone syn-collisional and post-collisional metallogenic overprinting. The YPCD is characterized by three pyrite-forming stages, namely a hydrothermal stage A (Py I), a syn-ductile deformation stage B (Py II) characterized by Cu-Au enrichment, and a fracture-filling stage C (Py III). In this study, we conducted systematic petrographic and geochemical studies of pyrites and coexist biotite, which formed during different stages, in order to constrain the physicochemical conditions of the ore formation. Euhedral, fragmented Py I has low Pb and high Te and Se concentration and Ni contents are low with Co/Ni ratios mostly between 1 and 10 (average 9.00). Py I is further characterized by enrichments of Bi, As, Ni, Cu, Te and Se in the core relative to the rim domains. Anhedral round Py II has moderate Co and Ni contents with high Co/Ni ratios >10 (average 95.2), and average contents of 46.5 ppm Pb and 5.80 ppm Te. Py II is further characterized by decreasing Bi, Cu, Pb, Zn, Ag, Te, Mo, Sb and Au contents from the rim to the core domains. Annealed Py III has the lowest Co content of all pyrite types with Co/Ni ratios mostly <0.1 (average 1.33). Furthermore, Py III has average contents of 3.31 ppm Pb, 1.33 ppm Te and 94.6 ppm Se. In addition, Fe does not correlate with Cu and S in the Py I and Py III, while Py II displays a negative correlation between Fe and Cu as well as a positive correlation between Fe and S. Therefore, pyrites which formed during different tectonic regimes also have different chemical compositions. Biotite geothermometer and oxygen fugacity estimates display increasing temperatures and oxygen fugacities from stage A to stage B, while temperature and oxygen fugacities decrease from stage B to stage C. The Co/Ni ratio of pyrite depends discriminates between the different mineralizing stages in the Yuleken porphyry copper deposit: Py II, associated with the deformation stage B and Cu-enrichment, shows higher Co/Ni ratios and enrichments of Pb, Zn, Mo, Te and Sb than the pyrites formed during the other two stages. The Co/Ni ratio of pyrite can not only apply to discriminate the submarine exhalative, magmatic or sedimentary origins for ore deposits but also can distinguish different ore-forming stages in a single porphyry Cu deposit. Thus, Co/Ni ratio of pyrites may act as an important exploration tool to distinguish pyrites from Cu-rich versus barren area. Furthermore, the distribution of Cu, Mo, Pb, Au, Bi, Sb and Zn in the variably deformed pyrite is proportional to the extent of deformation of the pyrites, indicating in accordance with variable physicochemical conditions different element migration behavior during the different stages of deformation and, thus, mineralisation.

Unshocked Equilibrated H Chondrites: A Common Low-Temperature Record from Fe-Mg Ordering in Orthopyroxene

NASA Astrophysics Data System (ADS)

Folco, L.; Mellini, M.; Pillinger, C. T.

1995-09-01

The study of the thermal metamorphism of ordinary chondrites through geothermometers can provide significant constraints on the parent body thermal models which remain controversial. We report here results from Fe-Mg ordering closure temperatures (Tc) of orthopyroxenes from eight unshocked equilibrated H-chondrites obtained by means of single crystal X-ray diffraction. The method is based on the fact that cation partitioning in orthopyroxene is sensitive to temperature [1], and makes use of the experimental calibration by Molin et al. [2]. The goal of the investigation is to check how petrographic types relate to cation ordering thermal records. Results: The orthopyroxenes show a very similar degree of Fe-Mg ordering (see Table 1.). The Tc's cluster within the 384+/-48 to 480+/-28 degrees C interval, and show no correlation with petrographic type. The lack of a correlation does not mean that the distribution is random, rather, it appears to be controlled in individual samples by the degree of equilibration. In fact, the higher the petrographic type, the more coherent the results of the grains from individual chondrites. The spread of Tc's in the least equilibrated chondrites could be either a memory of heterogeneous pre-metamorphic records related to individual chondrule histories, or an artefact due to crystal defects. Therefore (1) the thermal records, inferred from the Fe-Mg ordering, are nearly the same for all the equilibrated H-chondrites; (2) the most equilibrated chondrites record distinct Tc values within the larger common Tc range; (3) the spread of Tc in H4's maybe indicative of disequilibrium and merits further study. The closure temperature conveys information on the cooling rate close to its value, regardless of the temperature regimes when the ordering process started. Extrapolation to high temperatures can be made only if the cooling path is constrained. Since we have no data to establish the temperature when ordering began and to decide whether the cooling was linear, we have not attempted quantitative estimates of cooling rates. However we can say that as equilibrated H-chondrites carry similar Tc records, they cooled at similar rates through 380-480 degrees C. However, the k(sub)D's (i.e., the intracrystalline Fe-Mg distribution coefficient) range 0.029 to 0.054, suggesting that H-chondrites cooled in petrogenetic environments intermediate between those of volcanic [3] and granulitic rocks [3,4]. Conclusion: Our results provide the following constraints: (1) Equilibrated H-chondrites, regardless the petrographic type, were located in petrogenetic environments characterized by similar temperature-time conditions when cooling through 380-480 degrees C, and, in terms of terrestrial environments, intermediate between those of volcanic and granulitic facies. (2) Different petrographic types reflect distinct metamorphic thermal regimes. Thus, to account for constraint (1), petrographic type was determined at temperatures above the 380-480 degrees C interval. This implies that equilibrated H-chondrites were placed in different geological environments characterized by distinct temperature-time regimes when still above this temperature range. In the case of the least equilibrated chondrites, for which the two events could coincide. Acknowledgments: We thank EUROMET for providing us with the Frontier Mt. samples, and PNRA for supporting this study. References: [1] Saxena S. K. and Dal Negro A. (1983) Bull. Min ral., 106, 443-449. [2] Molin G. M. et al. (1991) EPSL, 105, 260-265. [3] Bertolo S. and Nimis P. (1993) EJM, 5, 707-719. [4] Tribaudino M. and Talarico F. (1992) EJM, 4, 453-463.

Thermodynamic modeling of non-ideal mineral-fluid equilibria in the system Si-Al-Fe-Mg-Ca-Na-K-H-O-Cl at elevated temperatures and pressures: Implications for hydrothermal mass transfer in granitic rocks

NASA Astrophysics Data System (ADS)

Dolejš, David; Wagner, Thomas

2008-01-01

We present the results of thermodynamic modeling of fluid-rock interaction in the system Si-Al-Fe-Mg-Ca-Na-H-O-Cl using the GEM-Selektor Gibbs free energy minimization code. Combination of non-ideal mixing properties in solids with multicomponent aqueous fluids represents a substantial improvement and it provides increased accuracy over existing modeling strategies. Application to the 10-component system allows us to link fluid composition and speciation with whole-rock mineralogy, mass and volume changes. We have simulated granite-fluid interaction over a wide range of conditions (200-600 °C, 100 MPa, 0-5 m Cl and fluid/rock ratios of 10-2-104) in order to explore composition of magmatic fluids of variable salinity, temperature effects on fluid composition and speciation and to simulate several paths of alteration zoning. At low fluid/rock ratios (f/r) the fluid composition is buffered by the silicate-oxide assemblage and remains close to invariant. This behavior extends to a f/r of 0.1 which exceeds the amount of exsolved magmatic fluids controlled by water solubility in silicate melts. With increasing peraluminosity of the parental granite, the Na-, K- and Fe-bearing fluids become more acidic and the oxidation state increases as a consequence of hydrogen and ferrous iron transfer to the fluid. With decreasing temperature, saline fluids become more Ca- and Na-rich, change from weakly acidic to alkaline, and become significantly more oxidizing. Large variations in Ca/Fe and Ca/Mg ratios in the fluid are a potential geothermometer. The mineral assemblage changes from cordierite-biotite granites through two-mica granites to chlorite-, epidote- and zeolite-bearing rocks. We have carried out three rock-titration simulations: (1) reaction with the 2 m NaCl fluid leads to albitization, chloritization and desilication, reproducing essential features observed in episyenites, (2) infiltration of a high-temperature fluid into the granite at 400 °C leads to hydrolytic alteration commencing with alkali-feldspar breakdown and leading to potassic, phyllic and argillic assemblages; this is associated with reduction and iron metasomatism as observed in nature and (3) interaction with a multicomponent fluid at 600 °C produces sodic-calcic metasomatism. Na, Ca and Fe are the most mobile elements whereas immobility of Al is limited by f/r ∼ 400. All simulations predict a volume decrease by 3.4-5.4%, i.e., porosity formation at f/r < 30. At higher fluid/rock ratios simulation (2) produces a substantial volume increase (59%) due to mineral precipitation, whereas simulation (3) predicts a volume decrease by 49% at the advanced albitization-desilication stage. Volume changes closely correlate with mass changes of SiO2 and are related to silica solubility in fluids. The combined effects of oxygen fugacity, fluid acidity and pH for breakdown of aqueous metal complexes and precipitation of ore minerals were evaluated by means of reduced activity products. Sharp increases in saturation indexes for oxidative breakdown occur at each alteration zone whereas reductive breakdown or involvement of other chloride complexes favor precipitation at high fluid/rock ratios only. Calculations of multicomponent aqueous-solid equilibria at high temperatures and pressures are able to accurately predict rock mineralogy and fluid chemistry and are applicable to diverse reactive flow processes in the Earth's crust.

Petrography and petrology of the Nornahraun eruption of the Bárðarbunga volcanic system, Iceland

NASA Astrophysics Data System (ADS)

Guðfinnsson, Guðmundur H.; Halldórsson, Sæmundur Ari; Bali, Enikő; Jakobsson, Sigurður; Sverrisdóttir, Guðrún; Höskuldssson, Ármann; Riishuus, Morten S.; Þórðarson, Þorvaldur; The 2014 Nornahraun Eruption Team

2015-04-01

The on-going fissure eruption north of Dyngjujökull is becoming the largest of its kind in Iceland since the 1783-84 Laki eruption. The erupted lava is olivine tholeiite, containing up to 5% normative olivine. It is relatively macrocryst-poor, initially containing less than 1% phenocrysts by volume, increasing to over 1% as the eruption has progressed. Plagioclase is the dominant macrocryst phase but olivine and augite are also present. In most of the samples, crystallization of the groundmass is substantial, with plagioclase and augite as the key groundmass minerals and minor olivine. It features subophitic texture, typical for olivine tholeiites, where the interstitial glass contains dendritic Fe-Ti oxide. During the first two months of the eruption, magma composition has been constant, displaying uniform major and trace element composition and nearly uniform isotopic compositions (Halldórsson et al. (a), this session). The major and trace element contents, in addition to the isotope ratios of lead, are indistinguishable from basalts in the Bárðarbunga volcanic system (Halldórsson et al. (b), this session). The compositional trends are consistent with crystallization along the ol-plag-cpx cotectic. Crystallization depth estimates, based on the pressure dependence of the cotectic (Yang et al., 1996), indicate that the magma equilibrated at a minimum depth between 6-9 km, consistent with depth estimates derived from CO2-bearing fluid inclusions trapped in plagioclase phenocrysts (Bali et al., this session). The bulk of the earthquakes associated with this volcano-tectonic episode are also in this range (e.g., Sigmundsson et al., 2015). Calculations with several different magma geothermometers suggest that the temperature of the magma as it rises to the surface is about 1170-1180°C, in good agreement with on-site measurements by thermal imaging cameras. The eruption has been characterized by steady, high emission of SO2. The sulfur-rich nature of the lava is also shown by the presence of sulfide globules in groundmass glass and sometimes as inclusions in groundmass minerals. The globules are always Fe-rich with considerable Cu and Ni contents and minor Co content. Sulfide globules are, however, missing in phenocryst phases crystallized at higher pressures, suggesting that sulfide saturation is a late process occurring during the crystallization of the groundmass minerals due to an increase in the sulfide content of the remaining melt. The presentation will contain more detailed petrographic observations and mineral chemistry of the eruption products that will be acquired with the newly installed EPMA (JEOL JXA-8230) at the Institute of Earth Sciences, University of Iceland. References: Bali et al., this session: Volatile budget of the Nornahraun eruption of the Bárðarbunga volcanic system, Iceland. Halldórsson et al. (a), this session: Geochemistry of the Nornahraun eruption of the Bárðarbunga volcanic system, Iceland. Halldórsson et al. (b), this session: Magma types and mantle sources of the Bárðarbunga volcanic system, Iceland Sigmundsson et al. (2015): Segmented lateral dyke growth in a rifting event at Bárðarbunga volcanic system, Iceland. Nature, in press. Yang et al. (1996): Experiments and models of anhydrous, basaltic olivine-plagioclase-augite saturated melts from 0.001 to 10 kbar. Contrib Mineral Petrol. 124 1-18.

Petrologic Applications of Tourmaline

NASA Astrophysics Data System (ADS)

London, D.; Morgan, G. B., VI; Wolf, M. B.; Guttery, B. M.

2011-12-01

Compositions of tourmaline reflect its chemical environment of formation. Schorl-dravite is an accessory in metapelites and persists up to the onset of anatexis. Amphibolites and marbles contain uvite, and magnesiofoitite-povandraite is distinctive of base-metal porphyries. In granitic pegmatites, schorl-dravite at the contacts evolves toward foitite and olenite (aluminous) components as Fe is depleted from the melt. Fractionation may bring residual melts to saturation in elbaite, an Li-rich component of tourmaline. Common tourmaline (schorl-dravite-olenite-foitite solid solution) possesses a wide P-T field of stability. Synthesis experiments put the upper thermal limit of common tourmaline at ~ 750°-850°C from 50 MPa to 10 GPa, and dravite has been synthesized as low as 350°C. The boron content of granitic melt or aqueous fluid in equilibrium with common tourmaline alone and with equivalent silicate mineral assemblages varies sharply with temperature according to a relationship of CB2O3melt,vapor ~ 0.0032e0.0087T(C). Common tourmaline is stable over an aSiO2 at and below saturation in Qtz; besides FeMg, its stability hinges principally on the solubility product [aAl2O3]3*[aB2O3]1.5 in vapor or melt. Surprisingly, increasing activities of H2O or fluoride components (both are present in tourmaline) destabilize common tourmaline in granitic melt, as both components form complexes with Al that reduce aAl2O3 in the melt. As a result, common tourmaline may survive anatexis when the aH2O attending melting is low. In contrast to common tourmaline, most attempts to synthesize elbaite have failed. Aluminous tourmaline containing 37 mol% Elb component has been synthesized recently, which is significant for understanding occurrences in pegmatites as well as for the potential appearance of synthetic elbaite on the gem market. Experimental calibration of δ11B between aqueous fluid and dravite at 50-500 MPa and 350°-750°C varies by only 6.1 % over this range of conditions (tourmaline is isotopically light with respect to the fluid), but it is pressure-dependent at least up to 200 MPa. This isotopic range is narrow in relation to vast tourmaline-producing magmatic-hydrothermal systems, such as the granites of Cornwall, UK. Preliminary experiments by Hervig et. al. (2002) report a large variation of Δ11B between aqueous fluid and granitic melt over small ranges of T, such that the isotopic composition of tourmaline should shift dramatically to higher (vapor) or lower (melt) values when crystallization occurs from a two-phase fluid system. Existing studies of consanguineous granite-pegmatite systems show nearly no variation of δ11B from common tourmaline in source granites to elbaite in the most fractionated pegmatites; the values correspond to those of tourmaline-melt, with little evidence for crystallization from vapor. Tourmaline may prove useful as a geothermometer in the same way as other AFM minerals, but the complexities of coupled substitutions in relation to the multitude of site occupancies in tourmaline will make experimental calibration a difficult, if not futile effort. Elemental fractionation between the polar ends of tourmaline, and its tendency for unidirectional growth, further complicate any quantitative treatment of its chemical composition.

Petrogenetic implications from ultramafic rocks and pyroxenites in ophiolitic occurrences of East Othris, Greece

NASA Astrophysics Data System (ADS)

Koutsovitis, P.; Magganas, A.

2012-04-01

Ultramafic rocks and pyroxenites in east Othris are included within ophiolitic units near the villages of Vrinena, Karavomilos, Pelasgia, Eretria, Agios Georgios, Aerino and Velestino. The first five ophiolitic occurrences are estimated to have been emplaced between the Oxfordian and Tithonian-Berriasian[1,2,3], while the latter two have been emplaced during the Eocene[4]. Ultramafic rocks include variably serpentinized harzburgites and lherzolites. Pyroxenites are usually found in the form of crosscutting veins within the harzburgites. Ultramafic rocks include depleted lherzolites, with Al2O3 ranging from 1.12 to 1.80 wt% and Cr from 3250 to 3290 ppm, as well as moderate to highly depleted serpentinized harzburgites, with Al2O3 ranging from 0.69 to 1.98 wt% and Cr from 2663 to 5582 ppm. Pyroxenites have generally higher Al2O3 ranging from 1.91 to 3.08 wt% and variable Cr ranging from 1798 to 3611 ppm. Lherzolites mostly include olivines (Fo=87.07-89.23) and clinopyroxenes (Mg#=85.71-90.12). Spinels from Eretria lherzolite (TiO2=0.02-0.08 wt%, Al2O3=36.06-42.45 wt%, Cr#=31.67-36.33) are compositionally similar with those of MORB peridotites[5], while those from Vrinena lherzolite (TiO2=0.16-0.43 wt%, Al2O3=6.90-22.12 wt%, Cr#=57.69-76.88) are similar to SSZ peridotites[5]. Serpentinized harzburgites include few olivines (Fo=90.51-91.15), enstatite porphyroclasts (Mg#=87.42-88.91), as well as fine grained enstatites of similar composition. Harzburgites from Pelasgia, Eretria and Agios Georgios include spinels (TiO2=0.03-0.08 wt%, Al2O3=23.21-31.58 wt%, Cr#=45.21-56.85) which do not clearly show if they are related with MORB or SSZ peridotites[5]. Spinels from Karavomilos harzburgite (TiO2=0.02-0.05 wt%, Al2O3=45.71-50.85 wt%, Cr#=16.84-22.32) are compositionally similar with MORB peridotites[5], whereas spinels from Vrinena harzburgite (TiO2=0.15-0.19 wt%, Al2O3=1.42-1.86 wt% Cr#=91.64-93.47) with SSZ peridotites[5]. Pyroxenites include clinopyroxenes (Mg#=84.25-91.78) but also enstatites (Mg#=88.37-91.47). Spinels have been analysed in pyroxenites from Aerino and Velestino (TiO2=0.79-1.07 wt%, Al2O3=10.88-18.46 wt% Cr#=60.74-70.78), indicating SSZ settings. Application of the olivine-spinel[6], olivine-augite[7], Cpx-Opx[8,9] geothermometers, yield equilibration temperatures of 961-1075 oC for lherzolites, 895-1084 oC for harzburgites and 990-1011 oC for pyroxenites. Our data indicate that the ophiolitic occurrences of Vrinena, Aerino and Velestino include ultramafic rocks and pyroxenites related to SSZ processes, while the other ophiolitic occurrences embrace ultramafic rocks which originated from a MORB-like setting, similar to west Othris ophiolites. It should be noted that even lherzolites have Cr and Y values similar to those of a highly depleted mantle source. A supra-subduction zone origin of the east Othris ophiolites, possibly with a slab rollback in the Pindos oceanic basin, may explain the different geotectonic environment affinities of the studied rocks.

Mantle temperatures, and tests of experimentally calibrated olivine-melt equilibria

NASA Astrophysics Data System (ADS)

Putirka, K. D.

2005-12-01

Because the ratio Mgol/Mgliq (Kd(Mg)) is sensitive to T, olivine-liquid Kd's have long been used as geothermometers, and more recently, maximum Fo contents from volcanic rocks have been used to estimate mantle potential temperatures. Such estimates by Putirka (2005, G3) indicate higher mantle equilibration temperatures at Hawaii, compared to temperatures derived from earlier calibrations. Several published models were thus tested for their ability to reproduce T for 862 experimental data. The Putirka (2005) models did not include P corrections, which are added here: lnKd(Mg)=-1.88 + 30.85P(GPa)/T(C) - 0.04[H2O]liq + 0.068[Na2O+K2O]liq + 3629.7/T(C) + 0.0087[SiO2]liq - 0.015[CaO]liq lnKd(Fe)= -2.92 - 0.05[H2O]liq + 0.0264[Na2O+K2O]liq + 2976.13/T(C) + 0.01847[SiO2]liq + 0.0171[Al2O3]liq - 0.039[CaO]liq + 33.17P(GPa)/T(C) In these expressions, Kd(Mg) and Kd(Fe) are the partition coefficients for Mg and Fe between olivine and liquid, expressed as cation fractions; compositional corrections are in weight percent. The models are calibrated from 785 experimental data (P = 0.0001-15.5 GPa; 1213-2353 K). In the tests, the expressions of Beattie (1993) performed exceptionally well for dry systems with MgOliq < 17 wt. %, with a standard error of estimate of 35 K, compared to an SEE of 59 K for Ford et al. (1983) and an SEE of 51 K for the inversion of the Kd(Mg) model above. Recalibration of the Beattie (1993) model over this composition range thus appears unnecessary. But Beattie (1993), Ford et al. (1983), and other models overestimate T for hydrous systems, and for compositions with MgOliq > 17 wt. %; new models are therefore needed. Over the greater compositional range, model 1 above can be inverted to yield T with a SEE of 56 K, and an average mean (systematic) error of +3 K for 856 experimental data; this compares to a systematic error of -26 K for Beattie (1993) and -36 K for Ford et al. (1983). For use in equation (1) of Putirka (2005), the models above are also more precise at both low and high MgO, and hydrous and non-hydrous systems compared to Beattie (1993) and Ford et al. (1983). Herzberg (pers. comm.) has modeled olivine-melt pairs for Hawaii and MOR's, which are in accord with Putirka (2005); these pairs are used to test for the effects of systematic model error on estimates of mantle temperatures. The Beattie (1993) and Ford (1983) models appear to predict too low a value for T (by 100-150 K), given comparisons of lnKd(Mg) v. 1/T(K) for experimental data, and the very low values for Kd(Mg) observed at Hawaii. The new calibrations indicate mantle equilibration temperatures of 1855 K at Hawaii and 1608 K at MOR's, in agreement with calculations by Putirka (2005). Excess temperatures at Hawaii thus likely exceed 200 K, as suggested by dynamic model predictions (Sleep, 1990; Schilling, 1991) for a thermal plume origin for the Hawaiian Islands and other hot spots.

Pressure - temperature estimates of a phengite eclogite from the Grapesvåre Nappe, Norrbotten, Swedish Caledonides

NASA Astrophysics Data System (ADS)

Bukała, Michał; Majka, Jarosław; Walczak, Katarzyna; Barnes, Christopher; Klonowska, Iwona

2017-04-01

The Seve Nappe Complex (SNC) of the Scandinavian Caledonides has well documented history of high pressure (HP) and ultra-high pressure (UHP) metamorphism (e.g. Klonowska et al. 2014). Eclogites of the SNC occur in two areas in Sweden, namely Jämtland and Norrbotten. The Jämtland eclogites and associated rocks are well studied and provide evidence for the Late Ordovician UHP metamorphism, whereas the Norrbotten eclogites, formed during the Late Cambrian/Early Ordovician, have not been studied in detail, especially in terms of pressure-temperature (P-T) conditions of their formation. Within the SNC in Norrbotten, eclogites are limited to two tectonic lenses - Vaimok and Tsäkkok (e.g. Albrecht, 2000). Within the Vaimok Lens three nappes have been distinguished: (1) the eclogite-free Lower Seve Nappe, (2) the Grapesvåre Nappe and (3) the Maddåive Nappe. The two latter nappes are eclogite-bearing. For this study eclogites were collected from the lowermost part of the Grapesvåre Nappe (from the highly heterogeneous Daunasvagge unit dominated by garnet-bearing mica schists, quartzites and marbles). Eclogite boudins (former dolerite dikes and sills) are usually highly altered due to retrogressive recrystallization. Rare fresh eclogites occur within large boudins (>5m in diameter) and display only minor alteration limited to the scarce veinlets composed of amphibole + feldspar + garnet + zoisite + biotite + rutile + titanite. Metamorphic peak conditions mineral assemblage consists of garnet + omphacite + phengite + quartz + rutile. For P-T estimates the geothermobarometric method of Ravna & Terry (2004) has been used. The garnet-clinopyroxene Fe2+-Mg exchange thermometer and the net-transfer reaction barometer based on the garnet-phengite-omphacite equilibrium yielded a maximum pressure of 26.7 kbar and temperature of 677°C. The obtained temperature might be underestimated due to uncertainties in Fe2+/Fe3+ ratio in pyroxene. Therefore Zr-in-rutile geothermometer by Tomkins et al. (2007) has also been used and calculcated temperatures are in a 715-762°C range. The obtained results are somewhat similar to scarce former P-T estimates of eclogites from Norrbotten provided by Santallier (1988) (i.e. T=690-730°C and Pmin=18.5-19.5 kbar) and Albrecht (2000) (i.e. T=650-720°C and P=18.9-27.5 kbar). However, as Albrecht (2000) claimed, pressure values might have been largely underestimated due to limitation of the used methods. Thus our study provides for the first time an evidence for near UHP metamorphism recorded by eclogites of the Grapesvåre Nappe, hence shedding a new light on evolution of the SNC in Norrbotten. We speculate that maximum pressures of metamorphism might have been higher (even approaching coesite stability field), but further studies are required to pinpoint the maximum PT conditions. This work is financially supported by the NCN "CALSUB" research project no. 2014/14/E/ST10/00321. References: Albrecht L.G. (2000) PhD thesis, Lund University. Klonowska I., Majka J., Janák M., Gee D.G., Ladenberger A. (2014) New Perspectives on the Caledonides of Scandinavia and Related Areas. Geological Society, London, Special Publications, 390: 321-336. Ravna E.J., Terry M.P. (2004) Journal of Metamorphic Geology 22: 579-592. Santallier D.S. (1988) Geologiska Föreningen i Stockholm Förhandlingar 110: 89-98. Tomkins H.S., Powell R., Ellis J.D. (2007) Journal of Metamorphic Geology 25: 703-713.

Formation of a paleothermal anomaly and disseminated gold deposits associated with the Bingham Canyon porphyry Cu-Au-Mo system, Utah

USGS Publications Warehouse

Cunningham, C.G.; Austin, G.W.; Naeser, C.W.; Rye, R.O.; Ballantyne, G.H.; Stamm, R.G.; Barker, C.E.

2004-01-01

The thermal history of the Oquirrh Mountains, Utah, indicates that hydrothermal fluids associated with emplacement of the 37 Ma Bingham Canyon porphyry Cu-Au-Mo deposit extended at least 10 km north of the Bingham pit. An associated paleothermal anomaly enclosed the Barneys Canyon and Melco disseminated gold deposits and several smaller gold deposits between them. Previous studies have shown the Barneys Canyon deposit is near the outer limit of an irregular distal Au-As geochemical halo, about 3 km beyond an intermediate Pb-Zn halo, and 7 km beyond a proximal pyrite halo centered on the Bingham porphyry copper deposit. The Melco deposit also lies near the outer limit of the Au-As halo. Analysis of several geothermometers from samples collected tip to 22 km north of the Bingham Canyon porphyry Cu-Au-Mo deposit indicate that most sedimentary rocks of the Oquirrh Mountains, including those at the gold deposits, have not been regionally heated beyond the "oil window" (less than about 150??C). For geologically reasonable heating durations, the maximum sustained temperature at Melco, 6 km north of the Bingham pit, and at Barneys Canyon, 7.5 km north of the pit, was between 100??C and 140??C, as indicated by combinations of conodont color alteration indices of 1.5 to 2, mean random solid bitumen reflectance of about 1.0 percent, lack of annealing of zircon fission tracks, and partial to complete annealing of apatite fission tracks. The pattern of reset apatite fission-track ages indicates that the gold deposits are located approximately on the 120??C isotherm of the 37 Ma paleothermal anomaly assuming a heating duration of about 106 years. The conodont data further constrain the duration of heating to between 5 ?? 104 and 106 years at approximately 120??C. The ??18O of quartzite host rocks generally increases from about 12.6 per mil at the porphyry to about 15.8 per mil approximately 11 km from the Bingham deposit. This change reflects interaction of interstitial clays in the quartzite with circulating meteoric water related to the Bingham Canyon porphyry system. The ??18O and ??13C values of limestone vary with respect to degree of recrystallization and proximity to open fractures. Recrystallized limestone at the Melco and Barneys Canyon gold deposits has the highest ??18O values (about 30???), whereas limestone adjacent to the porphyry copper deposit has the lowest values (about 10???). The high ??18O values for the recrystallized limestone at Barneys Canyon and Melco strongly suggest that mineralization was related to low temperature fluids with exceptionally high ??18OH2O values such as could be derived from water in a crater lake of an active volcano. The age of formation of the gold deposits has been interpreted to range from Jurassic to Eocene. The mineralized rocks at the Barneys Canyon and Melco deposits are likely the same age as the geochemically similar deposits that are present in north-striking, late faults that cut the Bingham Canyon porphyry. The patterns of apatite and zircon fission-track data, conodont color alteration indices, solid bitumen reflectivity, stable isotope data, and mineral zoning are consistent with the gold deposits being genetically related to formation of the 37 Ma Bingham porphyry deposit. We interpret the disseminated gold mineralization to be related to collapse of the Bingham Canyon hydrothermal system in which isotopically heavy, oxidizing, acidic waters, possibly from an internally draining acidic crater lake, mixed with and were entrained into reduced gold-bearing meteoric water fluids in the collapsing main-stage hydrothermal system. Most of this fluid mixing and cooling was probably located close to the hydrologic interface between the sedimentary basement rocks and overlying volcanic rocks. ??2004 by Economic Geology.

Temperature data from wells in Long Valley Caldera, California

USGS Publications Warehouse

Farrar, Christopher; DeAngelo, Jacob; Williams, Colin; Grubb, Frederick; Hurwitz, Shaul

2010-01-01

The 30-by-20-km Long Valley Caldera (LVC) in eastern California (fig.1) formed at 0.76 Ma in a cataclysmic eruption that resulted in the deposition of 600 km? of Bishop Tuff outside the caldera rim (Bailey, 1989). By approximately 0.6 Ma, uplift of the central part of the caldera floor and eruption of rhyolitic lava formed the resurgent dome. The most recent eruptive activity in the area occurred approximately 600 yr ago along the Mono-Inyo craters volcanic chain (Bailey, 2004; Hildreth, 2004). LVC hosts an active hydrothermal system that includes hot springs, fumaroles, mineral deposits, and an active geothermal well field and power plant at Casa Diablo along the southwestern boundary of the resurgent dome (Sorey and Lewis, 1976; Sorey and others, 1978; Sorey and others, 1991). Electric power generation began in 1985 with about 10 Mwe net capacity and was expanded to about 40 Mwe (net) in 1991 (Campbell, 2000; Suemnicht and others, 2007). Plans for further expansion are focused mainly on targets in the caldera?s western moat (Sass and Priest, 2002) where the most recent volcanic activity has occurred (Hildreth, 2004). LVC has been the site of extensive research on geothermal resources and volcanic hazards (Bailey and others, 1976; Muffler and Williams, 1976; Miller and others, 1982; Hill and others 2002). The first geothermal exploratory drilling was done in the shallow (< 200 m deep) hydrothermal system at Casa Diablo in the 1960?s (McNitt, 1963). Many more boreholes were drilled throughout the caldera in the 1970?s and 1980?s by private industry for geothermal exploration and by the U.S. Geological Survey (USGS) and Sandia National Laboratory for volcanic and geothermal research and exploration. Temperature logs were obtained in some of these wells during or immediately following drilling, before thermal equilibration was complete. Most of the temperature logs, however, were obtained weeks, months, or years after well completion and are representative of dynamic thermal equilibrium. The maximum reservoir temperature for LVC is estimated to be about 220?C on the basis of chemical geothermometers (Fournier and Truesdell, 1973) using analytical results from water samples collected from a large number of wells and springs across the caldera and around its periphery (Lewis, 1974; Mariner and Wiley, 1976; Farrar and others, 1985, 1987, 1989, White and Peterson, 1991). The deepest well in LVC (~3 km) is the Long Valley Exploratory Well (LVEW) drilled in the 1990?s with funding from the U.S. Department of Energy to investigate the potential for near-magmatic-temperature energy extraction and the occurrence of magma under the central part of the resurgent dome (Finger and Eichelberger, 1990; Finger and Jacobsen, 1999; Sackett and others, 1999). However, temperatures beneath the resurgent dome have proved disappointingly low and in LVEW reach a maximum of only 102 degrees C in a long isothermal section (2,100 to 3,000 m) in Mesozoic basement rocks (Farrar and others, 2003). Temperature data from well logs and geothermometry reveal that the highest temperatures in LVC are beneath the western moat. The hottest temperatures measured in LVC exceed 200 degrees C in two wells (44-16 and RDO-8) located in the western moat. Well 44-16 was drilled through the entire thickness of post-caldera volcanic fill and bottomed in Mesozoic basement. Well RDO-8 was drilled through post-caldera volcanic rocks and 305 m into the Bishop Tuff (Wollenberg and others, 1986). Temperatures in the hydrothermal system decrease toward the east by processes of conduction and dilution from cold groundwater recharge that occurs mostly around the caldera margin and beneath the resurgent dome. Reservoir temperatures at Casa Diablo (fig.1) are about 170?C (for example, MBP-3 and Mammoth-1), decreasing to about 100 degrees C in wells near Hot Creek Gorge (for example, MW-4 and CH-10B), and are generally less than 50?C in thermal springs near Lake

Metamorphic mineral assemblages of slightly calcic pelitic rocks in and around the Taconic Allochthon, southwestern Massachusetts and adjacent Connecticut and New York

USGS Publications Warehouse

Zen, E-an

1981-01-01

The mineral assemblages from metamorphosed slightly calcic pelitic rocks of the Taconic Range in southwestern Massachusetts and adjacent areas of Connecticut and New York were studied petrographically and chemically. These rocks vary in metamorphic grade from those below the chloritoid zone through the chloritoid and garnet zones into the kyanite-staurolite zone. Microprobe data on the ferromagnesian minerals show that the sequence of increasing Fe/ (Fe+Mg) value is, from the lowest, chlorite, biotite, hornblende, chloritoid, staurolite, garnet. Hornblende, epidote, garnet, and plagioclase are the most common minerals that carry significant calcium. Biotite is persistently deficient in alkali but is abnormally rich in octahedral aluminum to such an extent that the overall charge balance can be ascribed to an AI=K+ (Fe,Mg) diadochy. Muscovite contains small though persistent amounts of iron and magnesium in octahedral positions but has a variable K/Na ratio, which is potentially useful as a geothermometer. One low-grade muscovite is highly phengitic, but the white micas in rocks from metamorphic grades higher than chloritoid zone do not contain significant phengite components. Chlorite is persistently high in aluminum and so its ratio of divalent ions to aluminum is approximately that of garnet. Many garnets show pronounced zoning in manganese and less pronounced zoning in calcium. Garnet coexisting with hornblende contains a high proportion of the grossularitic component. The calcium content is significant in all the analyzed garnets, except those from a cummingtonite-bearing sample that is free of muscovite. This suggests that in slightly calcic pelitic rocks, calcium-free garnet cannot coexist with muscovite. Most of the mineral assemblages formed in the presence of excess quartz and muscovite. The phase-petrologic analysis, made with the aid of an eight-phase multisystematic model, shows the following major points: 1. Chloritoid and staurolite coexist in a definite interval of prograde metamorphism. 2. Biotite-chloritoid does not constitute an alternative assemblage to garnet-chlorite-muscovite, because the former combination is found predominantly in the presence of the latter combination. Because the garnet contains lime, all five phases are stable together in lowlime pelitic rocks. 3. The first appearance of staurolite in the area does not correspond to the reaction leading to the first intrinsic stable existence of this phase. Inasmuch as the first appearanc,e of staurolite is always in chlorite-bearing as semblages, I suggest that the mapped staurolite zone marker corresponds to a reaction whereby staurolitechlorite becomes stable. The probable lower grade chemical equivalent, for example, chloritoid-aluminum silicate, however, has not been found in the area of study. Several staurolite-forming reactions discussed in the literature are ruled out because of the relative siderophility of the minerals. A second staurolite isograd involves the reaction, chloritoid+chlorite+muscovite= staurolite+biotite. A third isograd involves staurolite+ chlorite=biotite+kyanite; this reaction is postulated on the basis of the observed assemblage biotite-kyanitesta urolite-garnet-muscoviteplagioclase-quartzilmenite. 4. In low-grade rocks, epidote is stable considerably before the first appearance of chloritoid. The nature of the high-aluminum phase in low-grade rocks that leads to the formation of chloritoid remains obscure. The epidote is always rich in ferric iron (pistacite content of about 1/ 4 to 1/3). Garnet-bearing assemblages (with or without epidote) are formed next as metamorphic grade increases. The next more calcium-rich silicate is hornblende, and despite the meager data on assemblages that include hornblende, the first intrinsic appearance of this phase has probably been recorded. At highstaurolite grade, the most calcium-rich assemblage in pelitic rocks is hornblende-garnet-biotite-plagioclase (bytownit

Thermochronological modeling of the age of Vologda crystalline basement of the Russian platform

NASA Astrophysics Data System (ADS)

Gerasimov, V. Yu.; Petrov, D. B.; Lebedev, V. A.

2010-05-01

The results of the complex petrological and isotope-geochronological study of the crystalline rock from the deep drilling hall of the south of Vologda segment are presented in this work. The crystalline basement of the platform in Vologda region lie in a depth 2.5 km and represented by high alumina mica schist. The thick sedimentary cover consists of vendian and phanerozoic sediments. Upper level covered by quaternary glacial deposits up to 50 m. A core sample from the borehole of Fedotovo village was obtained from the depth 2600 m. It is fine-medium grained metamorphic mica schist with sillimanite. The mineral assemblage represented by association: Pl-Bt-Ms-Sil-Qtz-Mag +Zrn +Mnz. The metamorphic schist of the crystalline basement contains several radio isotope sensors. There are two rock forming potassium reach mica, - biotite (Bt) and muscovite (Ms) and accessories monazite (Mnz), - the phosphate of REE enriched by Th and U. It was a reason why traditional K-Ar isotope dating method in the combination with electron microprobe U-Th-Pb dating method CHIME [Suzuki et al. 1991] was used for Vologda metapelite rocks dating. In addition to geochronology, the detailed petrological investigation using electron microprobe allowed also to determine thermodynamic parameters of metamorphic system with a help of the mineral thermobarometry and finally estimate the age of the metamorphic thermal event using experimental diffusion data of Ar and Pb in minerals [Gerasimov et al. 2004]. The temperature of the regional metamorphism was estimated using Bt+Mag+Qtz and Bt+Ms geothermometers [Glassley 1983, Hoisch 1989]. Taking into account the field of the sillimanite P-T stability it is possible to conclude that the peak of metamorphism was reached at temperature about ТоС=550+/-30° C and pressure Р=4+/-1 kbar. Isotope thermochronology of the sample demonstrate nearly Svecofenian age 1.7-1.8 Ga of Vologda crystalline basement. K-Ar isotope dating of black and white mica demonstrates regular progression of ages in a concordance with closure temperature of each mineral. The apparent Bt age is about 1670 Ma and Ms age is 1710 Ma. The estimation of closure temperature (Tc) for each of the minerals using Dodsn's theory [Dodson 1973] and DCT computer program with concordance procedure of cooling rate simulation for the two coexisting minerals demonstrate value 340° C and и 460° C for Bt and Ms respectively. The rate of cooling in this temperature range is about 3° C/Ma and time span between closure temperatures of the two micas is about 40 Ma. The value of the cooling rate is a very typical for regional metamorphism conditions. The linear extrapolation of the simulated time-temperature trend to the thermal peak of the regional metamorphism (estimated by mineral equilibriums at 550° C) demonstrates that cooling of the metamorphic system from the thermal peak to 460° C(closure temperature of Ms) takes about 30-40 Ma. It is a value of systematic thermochronological correction to the muscovite apparent K-Ar age which has to be added to estimate the age of regional metamorphism, after that we finally receive the age 1750+/-40 Ma. U-Th-Pb system of monazite grains was tested by electron microprobe JEOL 8200 in IGEM RAS using CHIME method. The analysis of 8 grains demonstrated averaged value of age 1790+/-55 Ma. It is in a very good agreement with K-Ar isotope dating results. Moreover, the estimation of monazite closure temperature using experimental data of Pb diffusion [Smith & Giletti 1997] shows the value Tc=540-560° C which almost exactly corresponds to the peak temperature of regional metamorphism. It is also an explanation of the very close results of dating in different isotope systems (conservative U-Th-Pb system of monazite and flexible K-Ar system) in the condition of slow cooling and demonstrates the thermochronological modeling effectiveness.

Thermal history of type-3 chondrites in the NASA antarctic collection

NASA Astrophysics Data System (ADS)

Bonal, L.; Quirico, E.; Montagnac, G.

2014-07-01

Chondrites are the most primitive meteorites. However, they were all modified in some ways by post-accretion geological processes operating on their asteroidal parent bodies. Hence, to decipher the formation(s) and origin(s) of their components, we must first understand how chondritic materials were modified in their asteroidal parent bodies. The modifications induced by secondary processes should not be underestimated and have to be precisely estimated before any interpretation of chondrite properties in terms of cosmochemistry. In particular, all chondrites contain some organic components that were potentially chemically and physically modified through post-accretion processes. A thin understanding of the induced evolution is required to allow for pertinent comparisons with other primitive extraterrestrial materials, such as cometary grains, to finally address questions such as the origin of organics in the Solar System. Type 3 chondrites experienced thermal metamorphism on their asteroidal parent body due to the radioactive decay of elements such as ^{26}Al. Temperatures higher than 300 °C were experienced on timescales of several thousands of years. Still, type 3 chondrites remain as unequilibrated rocks and common mineralogical thermometers cannot be applied. The polyaromatic carbonaceous matter is sensitive to thermal episodes (of long and short duration) experienced by the host meteorite. In particular, its structural order directly reflects the thermal history experienced on their parent bodies. The structural modification of the aromatic carbonaceous matter towards a higher order is irreversible, and independent of the mineralogy and degree of aqueous alteration. It is mainly controlled by the peak metamorphic temperature. Moreover, under the assumption of fairly similar organic precursors among chondrites of distinct groups, the structural order of polyaromatic organic matter allows for a direct comparison of their metamorphic grades. It is then possible to evaluate the metamorphic grade of the objects and to assign a petrologic type along a unique petrologic scale [1-4]. This technique has been successfully applied to type 3 Unequilibrated Ordinary Chondrites [1], carbonaceous CV chondrites [2], and CO chondrites [3]. The interpretation of the structural order of the polyaromatic carbonaceous matter in terms of thermal history is thus reliable. Raman spectroscopy enables the determination of the degree of structural order of the polyaromatic organic matter present in the matrix of chondrites. Both falls and finds, from Antarctica [4] and elsewhere, have been analyzed. It does not require a large amount of samples and is relatively easy to implement. Raman spectroscopy is particularly sensitive to the lowest petrologic types (3.0-3.2). The present NASA collection of Antarctic meteorites represents an incredible source of precious samples for our community. The present work finely characterizes the thermal history of most of the type 3 chondrites (UOCs, CVs, and COs) from that collection. At the present time, the objectives are threefold: (i) determination of reliable petrologic types indispensable for our community; (ii) identification of the most primitive type 3 chondrites (petrologic type ≤ 3.1); and (iii) identification of potential ''anomalous'' samples having experienced a slightly different thermal history. The JSC Meteorite Working Group generously allocated us with more than 150 chondrites (UOCs, CVs, and COs). The following points summarize the main results. (i) At the present time, the thermal histories of more than 100 samples have been characterized. (ii) The terrestrial weathering experienced by several chondrites (˜25 chondrites) has been too pervasive for the method to be applied. For these meteorites, as signatures of oxide minerals dominate Raman spectra of the matrix, the organic matter might have been significantly altered through oxidation. (iii) Real discrepancies with the preliminary JSC petrologic type attributions were found for several chondrites with mostly underestimations of the metamorphic grades. (iv) The structural grade of the polyaromatic carbonaceous matter is fairly homogeneous in most of the considered chondrites with a few exceptions, interpreted in terms of shock events. (v) Recently, there were some promising advances (e.g. [5,6]) in terms of interpretation of the structural order of the polyaromatic carbonaceous matter as a geothermometer for terrestrial rocks of low maturity grades. The used spectral tracers will be considered and the thermometry potentially applied to infer new constraints on the metamorphic temperature experienced by these type 3 chondrites.

Hydrogeologic framework and occurrence, movement, and chemical characterization of groundwater in Dixie Valley, west-central Nevada

USGS Publications Warehouse

Huntington, Jena M.; Garcia, C. Amanda; Rosen, Michael R.

2014-01-01

Dixie Valley, a primarily undeveloped basin in west-central Nevada, is being considered for groundwater exportation. Proposed pumping would occur from the basin-fill aquifer. In response to proposed exportation, the U.S. Geological Survey, in cooperation with the Bureau of Reclamation and Churchill County, conducted a study to improve the understanding of groundwater resources in Dixie Valley. The objective of this report is to characterize the hydrogeologic framework, the occurrence and movement of groundwater, the general water quality of the basin-fill aquifer, and the potential mixing between basin-fill and geothermal aquifers in Dixie Valley. Various types of geologic, hydrologic, and geochemical data were compiled from previous studies and collected in support of this study. Hydrogeologic units in Dixie Valley were defined to characterize rocks and sediments with similar lithologies and hydraulic properties influencing groundwater flow. Hydraulic properties of the basin-fill deposits were characterized by transmissivity estimated from aquifer tests and specific-capacity tests. Groundwater-level measurements and hydrogeologic-unit data were combined to create a potentiometric surface map and to characterize groundwater occurrence and movement. Subsurface inflow from adjacent valleys into Dixie Valley through the basin-fill aquifer was evaluated using hydraulic gradients and Darcy flux computations. The chemical signature and groundwater quality of the Dixie Valley basin-fill aquifer, and potential mixing between basin-fill and geothermal aquifers, were evaluated using chemical data collected from wells and springs during the current study and from previous investigations. Dixie Valley is the terminus of the Dixie Valley flow system, which includes Pleasant, Jersey, Fairview, Stingaree, Cowkick, and Eastgate Valleys. The freshwater aquifer in the study area is composed of unconsolidated basin-fill deposits of Quaternary age. The basin-fill hydrogeologic unit can be several orders of magnitude more transmissive than surrounding and underlying consolidated rocks and Dixie Valley playa deposits. Transmissivity estimates in the basin fill throughout Dixie Valley ranged from 30 to 45,500 feet squared per day; however, a single transmissivity value of 0.1 foot squared per day was estimated for playa deposits. Groundwater generally flows from the mountain range uplands toward the central valley lowlands and eventually discharges near the playa edge. Potentiometric contours east and west of the playa indicate that groundwater is moving eastward from the Stillwater Range and westward from the Clan Alpine Mountains toward the playa. Similarly, groundwater flows from the southern and northern basin boundaries toward the basin center. Subsurface groundwater flow likely enters Dixie Valley from Fairview and Stingaree Valleys in the south and from Jersey and Pleasant Valleys in the north, but groundwater connections through basin-fill deposits were present only across the Fairview and Jersey Valley divides. Annual subsurface inflow from Fairview and Jersey Valleys ranges from 700 to 1,300 acre-feet per year and from 1,800 to 2,300 acre-feet per year, respectively. Groundwater flow between Dixie, Stingaree, and Pleasant Valleys could occur through less transmissive consolidated rocks, but only flow through basin fill was estimated in this study. Groundwater in the playa is distinct from the freshwater, basin-fill aquifer. Groundwater mixing between basin-fill and playa groundwater systems is physically limited by transmissivity contrasts of about four orders of magnitude. Total dissolved solids in playa deposit groundwater are nearly 440 times greater than total dissolved solids in the basin-fill groundwater. These distinctive physical and chemical flow restrictions indicate that groundwater interaction between the basin fill and playa sediments was minimal during this study period (water years 2009–11). Groundwater in Dixie Valley generally can be characterized as a sodium bicarbonate type, with greater proportions of chloride north of the Dixie Valley playa, and greater proportions of sulfate south of the playa. Analysis of major ion water chemistry data sampled during the study period indicates that groundwater north and south of Township 22N differ chemically. Dixie Valley groundwater quality is marginal when compared with national primary and secondary drinking-water standards. Arsenic and fluoride concentrations exceed primary drinking water standards, and total dissolved solids and manganese concentrations exceed secondary drinking water standards in samples collected during this study. High concentrations of boron and tungsten also were observed. Chemical comparisons between basin-fill and geothermal aquifer water indicate that most basin-fill groundwater sampled could contain 10–20 percent geothermal water. Geothermal indicators such as high temperature, lithium, boron, chloride, and silica suggest that mixing occurs in many wells that tap the basin-fill aquifer, particularly on the north, south, and west sides of the basin. Magnesium-lithium geothermometers indicate that some basin-fill aquifer water sampled for the current study likely originates from water that was heated above background mountain-block recharge temperatures (between 3 and 15 degrees Celsius), highlighting the influence of mixing with warm water that was possibly derived from geothermal sources.

Determination of Uniaxial Compressive Strength of Ankara Agglomerate Considering Fractal Geometry of Blocks

NASA Astrophysics Data System (ADS)

Coskun, Aycan; Sonmez, Harun; Ercin Kasapoglu, K.; Ozge Dinc, S.; Celal Tunusluoglu, M.

2010-05-01

The uniaxial compressive strength (UCS) of rock material is a crucial parameter to be used for design stages of slopes, tunnels and foundations to be constructed in/on geological medium. However, preparation of high quality cores from geological mixtures or fragmented rocks such as melanges, fault rocks, coarse pyroclastic rocks, breccias and sheared serpentinites is often extremely difficult. According to the studies performed in literature, this type of geological materials may be grouped as welded and unwelded birmocks. Success of preparation of core samples from welded bimrocks is slightly better than unwelded ones. Therefore, some studies performed on the welded bimrocks to understand the mechanical behavior of geological mixture materials composed of stronger and weaker components (Gokceoglu, 2002; Sonmez et al., 2004; Sonmez et al., 2006; Kahraman, et al., 2008). The overall strength of bimrocks are generally depends on strength contrast between blocks and matrix; types and strength of matrix; type, size, strength, shape and orientation of blocks and volumetric block proportion. In previously proposed prediction models, while UCS of unwelded bimrocks may be determined by decreasing the UCS of matrix considering the volumetric block proportion, the welded ones can be predicted by considering both UCS of matrix and blocks together (Lindquist, 1994; Lindquist and Goodman, 1994; Sonmez et al., 2006 and Sonmez et al., 2009). However, there is a few attempts were performed about the effect of blocks shape and orientation on the strength of bimrock (Linqduist, 1994 and Kahraman, et al., 2008). In this study, Ankara agglomerate, which is composed of andesite blocks and surrounded weak tuff matrix, was selected as study material. Image analyses were performed on bottom, top and side faces of cores to identify volumetric block portions. In addition to the image analyses, andesite blocks on bottom, top and side faces were digitized for determination of fractal dimensions. To determine fractal dimensions of more than hundred andesite blocks in cores, a computer program namely FRACRUN were developed. Fractal geometry has been used as practical and popular tool to define particularly irregular shaped bodies in literature since the theory of fractal was developed by Mandelbrot (1967) (Hyslip and Vallejo, 1997; Kruhl and Nega, 1996; Bagde etal., 2002; Gulbin and Evangulova, 2003; Pardini, 2003; Kolay and Kayabali, 2006; Hamdi, 2008; Zorlu, 2009 and Sezer, 2009). Although there are some methods to determine fractal dimensions, square grid-cell count method for 2D and segment count method for 1D were followed in the algorithm of FRACRUN. FRACRUN has capable of determine fractal dimensions of many closed polygons on a single surface. In the study, a database composed of uniaxial compressive strength, volumetric block proportion, fractal dimensions and number of blocks for each core was established. Finally, prediction models were developed by regression analyses and compared with the empirical equations proposed by Sonmez et al. (2006). Acknowledgement This study is a product of ongoing project supported by TUBITAK (The Scientific and Technological Research Council of Turkey - Project No: 108Y002). References Bagde, M.N., Raina, A.K., Chakraborty, A.K., Jethwa, J.L., 2002. Rock mass characterization by fractal dimension. Engineering Geology 63, 141-155. Gokceoglu, C., 2002. A fuzzy triangular chart to predict the uniaxial compressive strength of the Ankara agglomerates from their petrographic composition. Engineering Geology, 66 (1-2), 39-51. Gulbin, Y.L., Evangulova, E.B., 2003. Morphometry of quartz aggregates in granites: fractal images referring to nucleation and growth processes. Mathematical Geology 35 (7), 819-833 Hamdi, E., 2008. A fractal description of simulated 3D discontinuity networks. Rock Mechanics and Rock Engineering 41, 587-599. Hyslip, J.P., Vallejo, L.E., 1997. Fractals analysis of the roughness and size distribution of granular materials. Engineering Geology 48, 231-244. Kahraman, S., Alber, M., Fener, M. and Gunaydin, O. 2008. Evaluating the geomechanical properties of Misis fault breccia (Turkey). Int. J. Rock Mech. Min. Sci, 45, (8), 1469-1479. Kolay, E., Kayabali, K., 2006. Investigation of the effect of aggregate shape and surface roughness on the slake durability index using the fractal dimension approach. Engineering Geology 86, 271-294. Kruhl, J.H., Nega, M., 1996. The fractal shape of sutured quartz grain boundaries: application as a geothermometer. Geologische Rundschau 85, 38-43. Lindquist E.S. 1994. The strength, deformation properties of melange. PhD thesis, University of California, Berkeley, 1994. 264p. Lindquist E.S. and Goodman R.E. 1994. The strength and deformation properties of the physical model m!elange. In: Nelson PP, Laubach SE, editors. Proceedings of the First North American Rock Mechanics Conference (NARMS), Austin, Texas. Rotterdam: AA Balkema; 1994. Pardini, G., 2003. Fractal scaling of surface roughness in artificially weathered smectite rich soil regoliths. Geoderma 117, 157-167. Sezer E., 2009. A computer program for fractal dimension (FRACEK) with application on type of mass movement characterization. Computers and Geosciences (doi:10.1016/j.cageo.2009.04.006). Sonmez H, Tuncay E, and Gokceoglu C., 2004. Models to predict the uniaxial compressive strength and the modulus of elasticity for Ankara Agglomerate. Int. J. Rock Mech. Min. Sci., 41 (5), 717-729. Sonmez, H., Gokceoglu, C., Medley, E.W., Tuncay, E., and Nefeslioglu, H.A., 2006. Estimating the uniaxial compressive strength of a volcanic bimrock. Int. J. Rock Mech. Min. Sci., 43 (4), 554-561. Zorlu K., 2008. Description of the weathering states of building stones by fractal geometry and fuzzy inference system in the Olba ancient city (Southern Turkey). Engineering Geology 101 (2008) 124-133.