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.

Geothermal Geodatabase for Routt Hot Springs, Routt County, Colorado

DOE Data Explorer

Richard Zehner

2012-11-01

This geodatabase was built to cover several geothermal targets developed by Flint Geothermal in 2012 during a search for high-temperature systems that could be exploited for electric power development. Several of the thermal springs and wells in the Routt Hot Spring and Steamboat Springs areahave geochemistry and geothermometry values indicative of high-temperature systems. Datasets include: 1. Results of reconnaissance shallow (2 meter) temperature surveys 2. Air photo lineaments 3. Groundwater geochemistry 5. Georeferenced geologic map of Routt County 6. Various 1:24,000 scale topographic maps

Chemistry Data for Geothermometry Mapping of Deep Hydrothermal Reservoirs in Southeastern Idaho

DOE Data Explorer

Earl Mattson

2016-01-18

This dataset includes chemistry of geothermal water samples of the Eastern Snake River Plain and surrounding area. The samples included in this dataset were collected during the springs and summers of 2014 and 2015. All chemical analysis of the samples were conducted in the Analytical Laboratory at the Center of Advanced Energy Studies in Idaho Falls, Idaho. This data set supersedes #425 submission and is the final submission for AOP 3.1.2.1 for INL. Isotopic data collected by Mark Conrad will be submitted in a separate file.

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

USGS Publications Warehouse

Wood, Warren W.; Low, Walton H.

1988-01-01

Geothermometry calculations of selected ground-water samples from known geothermal areas throughout the basin suggest that the geother- mal system is large in areal extent but has relatively low temperatures. Approximately half of the silica-quartz calculated water temperatures are greater than 90 °C. Radiocarbon dating of geothermal water in the Salmon Falls and Bruneau-Grand View areas in the south central part of the Snake River basin suggests that residence time of the geother- mal water is about 17,700 years.

An integrated study on microtectonics, geothermometry and thermochronology of the Çataldaǧ Core Complex (NW Turkey): Implications for cooling, deformation and uplift history

NASA Astrophysics Data System (ADS)

Kamaci, Omer; Altunkaynak, Safak

2017-04-01

We present an integrated study on structure, microstructure, geothermometry and thermochronology of the Çataldaǧ Core Complex (ÇCC) in NW Turkey in order to understand the cooling, deformation and uplift mechanisms. ÇCC is formed from an Eo-Oligocene granite-gneiss-migmatite complex (GGMC) and an Early Miocene I-type granodioritic body (ÇG: Çataldaǧ granodiorite) which were exhumed as a dome-shaped core complex in the footwall of a ring-shaped low-angle detachment zone (The Çataldaǧ Detachment Fault Zone; ÇDFZ) in the Early Miocene. New U-Pb zircon (LA-ICPMS) and monazite ages of GGMC yielded magmatic ages of 33.8 and 30.1 Ma (Latest Eocene-Early Oligocene). 40Ar/39Ar muscovite, biotite and K-feldspar from the GGMC yielded the deformation age span 21.38±0,05 Ma and 20.81±0.04 Ma, which is also the emplacement age (20.84±0.13 Ma and 21.6±0.04 Ma) of ÇG. ÇDFZ is responsible for mainly top-to-the-north sense kinematic processes. The microstructural features of quartz, feldspar and mica indicate that the ÇCC has undergone continuous deformations during its cooling, from submagmatic to cataclastic conditions. Five microstructural grades have been classified under ductile (DZ) and ductile-to-brittle shear zone (SZ), according to the estimated deformation temperature and intensity of the strain. Microcline twinning, marginally replacement myrmekite and flame-perthite are predominant features for feldspar while chessboard extinction, grain boundary migration and subgrain rotation recrystallization is common for quartz in the DZ which has a deformation temperature range of >600°C to 400°C. Grain size reduction is an important factor for the ductile to brittle shear zone (SZ). Feldspar is represented by bulging recrystallization (BLG), feldspar-fish and domino-type microfracture/microfaulting and quartz show more elongated structures such as ribbons with high aspect ratios. Mineral-fish (muscovite, biotite and feldspar) structures indicate a temperature range of 500°C to <250°C. The GGMC and ÇG, which were formed in different periods, suffered continuous ductile-to-brittle deformation and uplifted together along ÇDFZ during Early Miocene when the first major period of N-S extension began in the western Anatolia. Microstructural grades, two-feldspar geothermometry and geochronological data indicate that the GGMC and ÇG, which were formed in different periods, suffered continuous ductile-to-brittle deformation and uplifted together along ÇDFZ during Early Miocene when the first major period of N-S extension began in the western Anatolia.

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

Fluid inclusion and vitrinite-reflectance geothermometry compared to heat-flow models of maximum paleotemperature next to dikes, western onshore Gippsland Basin, Australia

USGS Publications Warehouse

Barker, C.E.; Bone, Y.; Lewan, M.D.

1999-01-01

Nine basalt dikes, ranging from 6 cm to 40 m thick, intruding the Upper Jurassic-Lower Cretaceous Strzelecki Group, western onshore Gippsland Basin, were used to study maximum temperatures (Tmax) reached next to dikes. Tmax was estimated from fluid inclusion and vitrinitereflectance geothermometry and compared to temperatures calculated using heat-flow models of contact metamorphism. Thermal history reconstruction suggests that at the time of dike intrusion the host rock was at a temperature of 100-135??C. Fracture-bound fluid inclusions in the host rocks next to thin dikes ( 1.5, using a normalized distance ratio used for comparing measurements between dikes regardless of their thickness. In contrast, the pattern seen next to the thin dikes is a relatively narrow zone of elevated Rv-r. Heat-flow modeling, along with whole rock elemental and isotopic data, suggests that the extended zone of elevated Rv-r is caused by a convection cell with local recharge of the hydrothermal fluids. The narrow zone of elevated Rv-r found next to thin dikes is attributed to the rise of the less dense, heated fluids at the dike contact causing a flow of cooler groundwater towards the dike and thereby limiting its heating effects. The lack of extended heating effects suggests that next to thin dikes an incipient convection system may form in which the heated fluid starts to travel upward along the dike but cooling occurs before a complete convection cell can form. Close to the dike contact at X/D 1.5. ?? 1998 Elsevier Science B.V. All rights reserved.

Native iron in the continental lower crust - Petrological and geophysical implications

NASA Technical Reports Server (NTRS)

Haggerty, S. E.; Toft, P. B.

1985-01-01

Lower crustal granulite xenoliths recovered from a kimberlite pipe in western Africa contain native iron (Fe) as a decomposition product of garnet and ilmenite. Magnetic measurements show that less than 0.1 percent (by volume) of iron metal is present. Data from geothermometry and oxygen geobarometry indicate that the oxide and metal phases equilibrated between iron-wuestite and magnetite-wuestite buffers, which may represent the oxidation state of the continental lower crust, and the depleted lithospheric upper mantle. Ferromagnetic native iron could be stable to a depth of about 95 kilometers and should be considered in the interpretation of long-wavelength static magnetic anomalies.

Native iron in the continental lower crust - Petrological and geophysical implications

NASA Astrophysics Data System (ADS)

Haggerty, S. E.; Toft, P. B.

1985-08-01

Lower crustal granulite xenoliths recovered from a kimberlite pipe in western Africa contain native iron (Fe) as a decomposition product of garnet and ilmenite. Magnetic measurements show that less than 0.1 percent (by volume) of iron metal is present. Data from geothermometry and oxygen geobarometry indicate that the oxide and metal phases equilibrated between iron-wuestite and magnetite-wuestite buffers, which may represent the oxidation state of the continental lower crust, and the depleted lithospheric upper mantle. Ferromagnetic native iron could be stable to a depth of about 95 kilometers and should be considered in the interpretation of long-wavelength static magnetic anomalies.

Fluid inclusion geothermometry

USGS Publications Warehouse

Cunningham, C.G.

1977-01-01

Fluid inclusions trapped within crystals either during growth or at a later time provide many clues to the histories of rocks and ores. Estimates of fluid-inclusion homogenization temperature and density can be obtained using a petrographic microscope with thin sections, and they can be refined using heating and freezing stages. Fluid inclusion studies, used in conjunction with paragenetic studies, can provide direct data on the time and space variations of parameters such as temperature, pressure, density, and composition of fluids in geologic environments. Changes in these parameters directly affect the fugacity, composition, and pH of fluids, thus directly influencing localization of ore metals. ?? 1977 Ferdinand Enke Verlag Stuttgart.

Development of inverted metamorphic isograds in the western metamorphic belt, Juneau, Alaska

USGS Publications Warehouse

Himmelberg, G.R.; Brew, D.A.; Ford, A.B.

1991-01-01

An inverted metamorphic gradient is preserved in the western metamorphic belt near Juneau, Alaska. Detailed mapping of pelitic single-mineral isograds, systematic changes in mineral assemblages, and silicate geothermometry indicate that thermal peak metamorphic conditions increase structurally upward over a distance of about 8 km. Silicate geobarometry suggests that the thermal peak metamorphism occurred under pressures of 9-11 kbar. Our preferred interpretation of the cause of the inverted gradient is that it formed during compression of a thickened wedge of relatively wet and cool rocks in response to heat flow associated with the formation and emplacement of tonalite sill magma. -from Authors

A CO2-Silica Geothermometer for Low Temperature Geothermal Resource Assessment, with Application to Resources in the Safford Basin, Arizona

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

Witcher, James C.; Stone, Claudia

1983-11-01

Geothermics is the study of the earth's heat energy, it's affect on subsurface temperature distribution, it's physical and chemical sources, and it's role in dynamic geologic processes. The term, geothermometry, is applied to the determination of equilibrium temperatures of natural chemical systems, including rock, mineral, and liquid phases. An assemblage of minerals or a chemical system whose phase composition is a function of temperature and pressure can be used as a geothermometer. Thus a geothermometer is useful to determine the formation temperature of rock or the last equilibrium temperature of a flowing aqueous solution such as ground water and hydrothermalmore » fluids.« less

Application of thermodynamics to silicate crystalline solutions

NASA Technical Reports Server (NTRS)

Saxena, S. K.

1972-01-01

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

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

NASA Astrophysics Data System (ADS)

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

2013-01-01

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

New Peak Temperature Constraints Using RSCM Geothermometry on Lucia Subterrane in Franciscan Complex (California, USA): Detection of Thermal Anomalies in Gold-Bearing Quartz Veins Surrounding.

NASA Astrophysics Data System (ADS)

Lahfid, A.; Delchini, S.; Lacroix, B.

2015-12-01

The occurrence of deposits hosted by carbonaceous materials-rich metasediments is widespread. Therefore, we aims in this study to investigate the potential of the Raman Spectroscopy of Carbonaceous Material (RSCM) geothermometry to detect thermal anomalies in hydrothermal ore deposits environment and to demonstrate the ability of warm fluids, migrating through the sedimentary sequence to locally disturb the thermal gradient and associated peak temperatures. For this purpose, we have chosen the Lucia subterrane in the Franciscan Complex (California, USA), which includes gold-bearing quartz veins that witness a hydrothermal overprint (Underwood et al., 1995).The sediments in this zone essentially comprise greywacke and shale-matrix mélange (e.g. Frey and Robinson, 1999), which have undergone high-pressure, low-temperature metamorphism. The thermal history of the Lucia subterrane has been previously proposed by Underwood et al. (1995), essentially using vitrinite reflectance method (Rm). Rm values increase from the south to the north; they vary between 0.9 and 3.7 % (~150-280°C). All these results suggest that the Lucia subterrane underwent a regional increase of thermal gradient toward the north. Anomalous Rm values from 4.5% to 4.9% (~305-315°C) are recorded near Cape San Martin. These highest temperatures estimated are likely, associated with a late hydrothermal event (Underwood et al., 1995). Estimated Raman temperatures 1) confirmed the increase in the metamorphic grade towards the north already shown by Underwood et al. (1995), using classical methods like mineralogy and vitrinite reflectance and 2) exhibit anomalous values (temperatures reach 350°C). These anomalies are probably due to the later hydrothermal event. This result suggests that RSCM could be used as a reliable tool to determine thermal anomalies caused by hot fluid-flow.

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

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.

Interpretation of Na-K-Mg relations in geothermal waters

USGS Publications Warehouse

Fournier, R.O.

1990-01-01

When using a Na-K-???Mg triangular diagram as an aid in the interpretation of a geothermal water, the estimated temperature of last water-rock equilibration may change by as much as 50??C, depending on which of the many Na/K geothermometers one assumes is correct. A particular geothermometer may work well in one place and not in another because of differences in the mineralogy of the phases that are in contact with the reservoir fluid. The position of the full equilibrium line that is used for geothermometry and for assessing degrees of departure from equilibrium also changes as the assumed K/???Mg geothermometer equation changes. The degree of ambiguity can be evaluated by utilizing the results of all the recently published Na/K geothermometers on a single Na-K-???Mg triangular plot.

Pre-eruptive storage conditions of the Holocene dacite erupted from Kizimen Volcano, Kamchatka

USGS Publications Warehouse

Browne, B.; Izbekov, P.; Eichelberger, J.; Churikova, T.

2010-01-01

This study describes an investigation of the pre-eruptive conditions (T, P and fO2) of dacite magma erupted during the KZI cycle (12,000-8400 years ago) of Kizimen Volcano, Kamchatka, the earliest, most voluminous and most explosive eruption cycle in the Kizimen record. Hydrothermal, water-saturated experiments on KZI dacite pumice coupled with titanomagnetite-ilmenite geothermometry calculations require that the KZI dacite existed at a temperature of 823 ?? 20??C and pressures of 125-150 MPa immediately prior to eruption. This estimate corresponds to a lithologic contact between Miocene volcaniclastic rocks and Pliocene-Pleistocene volcanic rocks located at a depth of 5-6 km beneath the Kizimen edifice, which may have facilitated the accumulation of atypically large volumes of gas-rich dacite during the KZI cycle.

Thermomagmatic evolution of Mesoproterozoic crust in the Blue Ridge of SW Virginia and NW North Carolina: Evidence from U-Pb geochronology and zircon geothermometry

USGS Publications Warehouse

Tollo, Richard P.; Aleinikoff, John N.; Wooden, Joseph L.; Mazdab, Frank K.; Southworth, Scott; Fanning, Mark C.

2010-01-01

New geologic mapping, petrology, and U-Pb geochronology indicate that Mesoproterozoic crust near Mount Rogers consists of felsic to mafic meta-igneous rocks emplaced over 260 m.y. The oldest rocks are compositionally diverse and migmatitic, whereas younger granitoids are porphyritic to porphyroclastic. Cathodoluminescence imaging indicates that zircon from four representative units preserves textural evidence of multiple episodes of growth, including domains of igneous, metamorphic, and inherited origin. Sensitive high-resolution ion microprobe (SHRIMP) trace-element analyses indicate that metamorphic zircon is characterized by lower Th/U, higher Yb/Gd, and lower overall rare earth element (REE) concentrations than igneous zircon. SHRIMP U-Pb isotopic analyses of zircon define three episodes of magmatism: 1327 ± 7 Ma, 1180–1155 Ma, and 1061 ± 5 Ma. Crustal recycling is recorded by inherited igneous cores of 1.33–1.29 Ga age in 1161 ± 7 Ma meta-monzogranite. Overlapping ages of igneous and metamorphic crystallization indicate that plutons of ca. 1170 and 1060 Ma age were emplaced during episodes of regional heating. Local development of hornblende + plagioclase + quartz ± clinopyroxene indicates that prograde metamorphism at 1170–1145 Ma and 1060–1020 Ma reached upper-amphibolite-facies conditions, with temperatures estimated using Ti-in-zircon geothermometry at ~740 ± 40 °C during both episodes. The chemical composition of 1327 ± 7 Ma orthogranofels from migmatite preserves the first evidence of arc-generated rocks in the Blue Ridge, indicating a subduction-related environment that may have been comparable to similar-age systems in inliers of the Northern Appalachians and the Composite Arc belt of Canada. Granitic magmatism at 1180–1155 Ma and ca. 1060 Ma near Mount Rogers was contemporaneous with anorthosite-mangerite-charnockite-granite (AMCG) plutonism in the Northern Appalachian inliers and Canadian Grenville Province. Metamorphism at ca. 1160 and 1060 Ma correlates temporally with the Shawinigan orogeny and Ottawan phase of the Grenvillian orogeny, respectively, suggesting that the Blue Ridge was part of Rodinia dating back to ca. 1180 Ma.

Spectral reflectance properties of carbon-bearing materials

NASA Technical Reports Server (NTRS)

Cloutis, Edward A.; Gaffey, Michael J.; Moslow, Thomas F.

1994-01-01

The 0.3-2.6 micrometers spectral reflectance properties of carbon polymorphs (graphite, carbon black, diamond), carbides (silicon carbide, cementite), and macromolecular organic-bearing materials (coal, coal tar extract, oil sand, oil shale) are found to vary from sample to sample and among groups. The carbon polymorphs are readily distinguishable on the basis of their visible-near infrared spectral slopes and shapes. The spectra of macromolecular organic-bearing materials show increases in reflectance toward longer wavelengths, exceeding the reflectance rise of more carbon-rich materials. Reflectance spectra of carbonaceous materials are affected by the crystal structure, composition, and degree of order/disorder of the samples. The characteristic spectral properties can potentially be exploited to identify individual carbonaceous grains in meteorites (as separates or in situ) or to conduct remote sensing geothermometry and identification of carbonaceous phases on asteroids.

Origin of a rhyolite that intruded a geothermal well while drilling at the Krafla volcano, Iceland

USGS Publications Warehouse

Elders, W.A.; Fridleifsson, G.O.; Zierenberg, R.A.; Pope, E.C.; Mortensen, A.K.; Gudmundsson, A.; Lowenstern, J. B.; Marks, N.E.; Owens, L.; Bird, D.K.; Reed, M.; Olsen, N.J.; Schiffman, P.

2011-01-01

Magma flowed into an exploratory geothermal well at 2.1 km depth being drilled in the Krafla central volcano in Iceland, creating a unique opportunity to study rhyolite magma in situ in a basaltic environment. The quenched magma is a partly vesicular, sparsely phyric, glass containing ~1.8% of dissolved volatiles. Based on calculated H2O-CO2 saturation pressures, it degassed at a pressure intermediate between hydrostatic and lithostatic, and geothermometry indicates that the crystals in the melt formed at ~900 ??C. The glass shows no signs of hydrothermal alteration, but its hydrogen and oxygen isotopic ratios are much lower than those of typical mantle-derived magmas, indicating that this rhyolite originated by anhydrous mantle-derived magma assimilating partially melted hydrothermally altered basalts. ?? 2011 Geological Society of America.

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

Geothermal Geodatabase for Rico Hot Springs Area and Lemon Hot Springs, Dolores and San Miguel Counties, Colorado

DOE Data Explorer

Richard Zehner

2012-11-01

This geodatabase was built to cover several geothermal targets developed by Flint Geothermal in 2012 during a search for high-temperature systems that could be exploited for electric power development. Several of the thermal springs have geochemistry and geothermometry values indicative of high-temperature systems. In addition, the explorationists discovered a very young Climax-style molybdenum porphyry system northeast of Rico, and drilling intersected thermal waters at depth. Datasets include: 1. Structural data collected by Flint Geothermal 2. Point information 3. Mines and prospects from the USGS MRDS dataset 4. Results of reconnaissance shallow (2 meter) temperature surveys 5. Air photo lineaments 6. Areas covered by travertine 7. Groundwater geochemistry 8. Land ownership in the Rico area 9. Georeferenced geologic map of the Rico Quadrangle, by Pratt et al. 10. Various 1:24,000 scale topographic maps

Shallow-storage conditions for the rhyolite of the 1912 eruption at Novarupta, Alaska

USGS Publications Warehouse

Coombs, Michelle L.; Gardner, James E.

2001-01-01

Recent studies have proposed contrasting models for the plumbing system that fed the 1912 eruption of Novarupta, Alaska. Here, we investigate the conditions under which the rhyolitic part of the erupted magma last resided in the crust prior to eruption. Geothermometry suggests that the rhyolite was held at ∼800-850 °C, and analyses of melt inclusions suggest that it was fluid saturated and contained ∼4 wt% water. Hydrothermal, water-saturated experiments on rhyolite pumice reveal that at those temperatures the rhyolite was stable between 40 and 100 MPa, or a depth of 1.8-4.4 km. These results suggest that pre-eruptive storage and crystal growth of the rhyolite were shallow; if the rhyolite ascended from greater depths, it did so slowly enough for unzoned phenocrysts to grow as it passed through the shallow crust.

Thermal Efficiency of Lava Tubes of the Pu'u O'o-Kupaianaha Eruption, Kilauea Volcano, Hawaii

NASA Astrophysics Data System (ADS)

Helz, R. T.; Heliker, C.; Hon, K.; Mangan, M. T.

2002-12-01

We have applied glass geothermometry to a suite of very glassy lava samples collected from the upper (pond) and lower (coast) ends of the Episode 48 tube system, throughout the lifetime of the Kupaianaha pond, and also to a small suite of skylight samples collected from various tubes active between 1987 and 1993. The results for the pond-coast pairs are: (1) From November 1986 through January 1988 (15 months), the average change in glass quenching temperature from pond to coast (for 12 pairs) is 12.4°C. The average increase in crystallinity (inferred from observed enrichment of TiO2 and K2O in the coastal glasses) is 11-12% by weight. (2) For the 23 months from February 1988 through November 1989, the average change in inferred quenching temperature (for 25 pairs) is 8.4°C. The average increase in crystallinity is 4-5% by weight. Within this part of the data set, pond and coastal temperatures rise and fall together much of the time, even though these temporal fluctuations are at or below the limit of resolution of glass geothermometry (ΔT < 3 degrees). (3) The minimum difference in temperature for any pond-coast pair is 7°C. Twenty-four (out of 37) pairs have ΔT = 7-9°C, over the three year period. About half of the skylight samples have glass MgO contents consistent with their linear position along the tube system. In other samples, the skylight glasses are displaced to lower MgO contents, suggesting that such samples are not consistently as well-quenched as the pond and littoral spatter samples. For the data from 1992-93, the new tube system was 2 km shorter than the earlier, Kupaianaha-fed tubes. The best-documented ΔT of 6°C for some 1993 samples observed for this 10-km long tube, gives exactly the same temperature decrease with distance (0.6°/km) as the limiting ΔT of 7°C observed for the 12-km Kupaianaha tube systems. This cooling rate may represent the limiting thermal efficiency of tubes of the current Kilauea East Rift eruption.

Alum Innovative Exploration Project (Ram Power Inc.)

DOE Data Explorer

Miller, Clay

2010-01-01

Data generated from the Alum Innovative Exploration Project, one of several promising geothermal properties located in the middle to upper Miocene (~11-5 Ma, or million years BP) Silver Peak-Lone Mountain metamorphic core complex (SPCC) of the Walker Lane structural belt in Esmeralda County, west-central Nevada. The geothermal system at Alum is wholly concealed; its upper reaches discovered in the late 1970s during a regional thermal-gradient drilling campaign. The prospect boasts several shallow thermal-gradient (TG) boreholes with TG >75oC/km (and as high as 440oC/km) over 200-m intervals in the depth range 0-600 m. Possibly boiling water encountered at 239 m depth in one of these boreholes returned chemical- geothermometry values in the range 150-230oC. GeothermEx (2008) has estimated the electrical- generation capacity of the current Alum leasehold at 33 megawatts for 20 years; and the corresponding value for the broader thermal anomaly extending beyond the property at 73 megawatts for the same duration.

In search of early life: Carbonate veins in Archean metamorphic rocks as potential hosts of biomarkers

NASA Astrophysics Data System (ADS)

Peters, Carl A.; Piazolo, Sandra; Webb, Gregory E.; Dutkiewicz, Adriana; George, Simon C.

2016-11-01

The detection of early life signatures using hydrocarbon biomarkers in Precambrian rocks struggles with contamination issues, unspecific biomarkers and the lack of suitable sedimentary rocks due to extensive thermal overprints. Importantly, host rocks must not have been exposed to temperatures above 250 °C as at these temperatures biomarkers are destroyed. Here we show that Archean sedimentary rocks from the Jeerinah Formation (2.63 billion yrs) and Carawine Dolomite (2.55 billion yrs) of the Pilbara Craton (Western Australia) drilled by the Agouron Institute in 2012, which previously were suggested to be suitable for biomarker studies, were metamorphosed to the greenschist facies. This is higher than previously reported. Both the mineral assemblages (carbonate, quartz, Fe-chlorite, muscovite, microcline, rutile, and pyrite with absence of illite) and chlorite geothermometry suggest that the rocks were exposed to temperatures higher than 300 °C and probably ∼400 °C, consistent with greenschist-facies metamorphism. This facies leads to the destruction of any biomarkers and explains why the extraction of hydrocarbon biomarkers from pristine drill cores has not been successful. However, we show that the rocks are cut by younger formation-specific carbonate veins containing primary oil-bearing fluid inclusions and solid bitumens. Type 1 veins in the Carawine Dolomite consist of dolomite, quartz and solid bitumen, whereas type 2 veins in the Jeerinah Formation consist of calcite. Within the veins fluid inclusion homogenisation temperatures and calcite twinning geothermometry indicate maximum temperatures of ∼200 °C for type 1 veins and ∼180 °C for type 2 veins. Type 1 veins have typical isotopic values for reprecipitated Archean sea-water carbonates, with δ13CVPDB ranging from - 3 ‰ to 0‰ and δ18OVPDB ranging from - 13 ‰ to - 7 ‰, while type 2 veins have isotopic values that are similar to hydrothermal carbonates, with δ13CVPDB ranging from - 18 ‰ to - 4 ‰ and δ18OVPDB ranging from - 18 ‰ to - 12 ‰. Evidently, the migration and entrapment of hydrocarbons occurred after peak metamorphism under temperatures congruous with late catagenesis and from fluids of different compositions. The relatively high temperatures of vein formation and the known geotectonic history of the rocks analysed suggest a probable minimum age of 1.8 billion yrs (Paleoproterozoic). Our results demonstrate that post peak-metamorphic veins provide an exciting opportunity in the search for evidence of early life. The integration of petrological and organic geochemical techniques is crucial for any future studies that use biomarkers to reconstruct the early biosphere.

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

NASA Astrophysics Data System (ADS)

Reiser, Martin Kaspar; Schuster, Ralf; Tropper, Peter; Fügenschuh, Bernhard

2017-04-01

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

Rock geochemistry related to mineralization processes in geothermal areas

NASA Astrophysics Data System (ADS)

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

2018-02-01

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

Washington Play Fairway Analysis Geothermal GIS Data

DOE Data Explorer

Corina Forson

2015-12-15

This file contains file geodatabases of the Mount St. Helens seismic zone (MSHSZ), Wind River valley (WRV) and Mount Baker (MB) geothermal play-fairway sites in the Washington Cascades. The geodatabases include input data (feature classes) and output rasters (generated from modeling and interpolation) from the geothermal play-fairway in Washington State, USA. These data were gathered and modeled to provide an estimate of the heat and permeability potential within the play-fairways based on: mapped volcanic vents, hot springs and fumaroles, geothermometry, intrusive rocks, temperature-gradient wells, slip tendency, dilation tendency, displacement, displacement gradient, max coulomb shear stress, sigma 3, maximum shear strain rate, and dilational strain rate at 200m and 3 km depth. In addition this file contains layer files for each of the output rasters. For details on the areas of interest please see the 'WA_State_Play_Fairway_Phase_1_Technical_Report' in the download package. This submission also includes a file with the geothermal favorability of the Washington Cascade Range based off of an earlier statewide assessment. Additionally, within this file there are the maximum shear and dilational strain rate rasters for all of Washington State.

Geothermal Reservoir Temperatures in Southeastern Idaho using Multicomponent Geothermometry

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

Neupane, Ghanashyam; Mattson, Earl D.; McLing, Travis L.

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

Improvements in geothermometry. Final technical report. Rev

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

Potter, J.; Dibble, W.; Parks, G.

1982-08-01

Alkali and alkaline earth geothermometers are useful for estimating geothermal reservoir temperatures, though a general theoretical basis has yet to be established and experimental calibration needs improvement. Equilibrium cation exchange between feldspars provided the original basis for the Na-K and Na-K-Ca geothermometers (Fournier and Truesdell, 1973), but theoretical, field and experimental evidence prove that neither equilibrium nor feldspars are necessary. Here, evidence is summarized in support of these observations, concluding that these geothermometers can be expected to have a surprisingly wide range of applicability, but that the reasons behind such broad applicability are not yet understood. Early experimental work provedmore » that water-rock interactions are slow at low temperatures, so experimental calibration at temperatures below 150/sup 0/ is impractical. Theoretical methods and field data were used instead for all work at low temperatures. Experimental methods were emphasized for temperatures above 150/sup 0/C, and the simplest possible solid and solution compositions were used to permit investigation of one process or question at a time. Unexpected results in experimental work prevented complete integration of the various portions of the investigation.« less

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.

McGee Mountain Geoprobe Survey, Humboldt County, Nevada

DOE Data Explorer

Richard Zehner

2010-01-01

This shapefile contains location and attribute data for a Geoprobe temperature survey conducted by Geothermal Technical Partners, Inc. during 2010. The purpose of direct push technology (“DPT”) probe activity at the McGee Mtn. Project, Nevada was to 1) determine bottom hole temperatures using nominal 1.5 inch probe tooling to place resistance temperature detectors (“RTD”) and 2) take water samples, if possible, to characterize the geothermometry of the system. A total of 23 holes were probed in five days for a cumulative total of 857.5 ft. at 21 sites at McGee Mountain. The probed holes ranged in depth from a maximum of 75 ft to a minimum of 10 ft and averaged 37.3ft. The average temperature of the 23 holes was 18.9⁰C, with a range of 12.0⁰C at site MMTG#1b to 42.0⁰C at site MMTG#19. . No water was encountered in any of the probed holes, with the exception of MMTG#10, and no water was collected for sampling. Zip file containing Arcview shapefile in UTM11 NAD83 projection. 5kb file size.

Hot springs, geochemistry, and regional heat flow of northcentral Mexico

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

Swanberg, C.A.; Marvin, P.R.; Salazar S., L.

1981-10-01

To date we have found, sampled and performed chemical analyses on 21 hot springs (T > 30/sup 0/C), 4 hot wells (T > 30/sup 0/C) and 15 warm springs (T = 25 to 30/sup 0/C) from the states of Chihuahua, Coahuila and Sonora, Mexico. Also in order to establish background chemistry, an additional 250 cold wells and springs (T = 12 to 25/sup 0/C) were sampled and analyzed and several hundred water analyses from the several thousand provided by various Mexican agencies were included. The technique of silica geothermometry was used to estimate the regional heat flow of northcentral Mexico.more » Both the traditional heat flow and the silica heat flow values are generally high and show considerable scatter as is typical of areas having Tertiary and Quaternary volcanic and tectonic activity. Specific areas of high heat flow (> 2.5 HFU) include the Presidio and Los Muertos Bolsons, the Cuidad Chihuahua-Chuatemoc area, the Delicias area, and the area south of the San Bernardino Bolson of southeast Arizona. Areas of lower heat flow (2.0 to 2.5 HFU) include the Jimenez-Camargo region and the area between the Los Muertos and Presidio Bolsons.« less

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

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

Eppler, D.B.; Heiken, G.; Wohletz, K.

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

The lateral boundary of a metamorphic core complex: The Moutsounas shear zone on Naxos, Cyclades, Greece☆

PubMed Central

Cao, Shuyun; Neubauer, Franz; Bernroider, Manfred; Liu, Junlai

2013-01-01

We describe the structure, microstructures, texture and paleopiezometry of quartz-rich phyllites and marbles along N-trending Moutsounas shear zone at the eastern margin of the Naxos metamorphic core complex (MCC). Fabrics consistently indicate a top-to-the-NNE non-coaxial shear and formed during the main stage of updoming and exhumation between ca. 14 and 11 Ma of the Naxos MCC. The main stage of exhumation postdates the deposition of overlying Miocene sedimentary successions and predates the overlying Upper Miocene/Pliocene conglomerates. Detailed microstructural and textural analysis reveals that the movement along the Moutsounas shear zone is associated with a retrograde greenschist to subgreenschist facies overprint of the early higher-temperature rocks. Paleopiezometry on recrystallized quartz and calcite yields differential stresses of 20–77 MPa and a strain rate of 10−15–10−13 s−1 at 350 °C for quartz and ca. 300 °C for calcite. Chlorite geothermometry of the shear zone yields two temperature regimes, 300–360 °C, and 200–250 °C. The lower temperature group is interpreted to result from late-stage hydrothermal overprint. PMID:26523079

Mixing of magmatic volatiles with groundwater and interaction with basalt on the summit of Kilauea Volcano, Hawaii

NASA Astrophysics Data System (ADS)

Hurwitz, Shaul; Goff, Fraser; Janik, Cathy J.; Evans, William C.; Counce, Dale A.; Sorey, Michael L.; Ingebritsen, Steven E.

2003-01-01

We interpret new chemical and isotopic data from samples collected between October 1998 and March 2002 from the NSF well (also called the Keller well), the only deep well on the summit of Kilauea Volcano, Hawaii. Sample collection followed cleaning of the well, which renewed access to the hydrothermal system very close to the loci of magmatic and fumarolic activity. The chemical and isotopic compositions of the new samples differ remarkably from data published previously. On the basis of the S/Cl ratio and carbon and helium isotopes we conclude that the thermal fluids formed by condensation of magmatic gas into shallow meteoric groundwater. Gas condensation was followed by a complex pattern of basalt dissolution accompanied by an increase of fluid pH and precipitation of secondary minerals. Geochemical modeling and geothermometry imply that the fluids equilibrated with an assemblage of secondary minerals at temperatures between 90 and 140°C. The significantly different chemical composition of the NSF well fluids from that of springs along the southern coast of the island indicates that mass transport from the summit region toward the lower flanks of the volcano is limited.

Structural analysis and deformation characteristics of the Yingba metamorphic core complex, northwestern margin of the North China craton, NE Asia

NASA Astrophysics Data System (ADS)

Yin, Congyuan; Zhang, Bo; Han, Bao-Fu; Zhang, Jinjiang; Wang, Yang; Ai, Sheng

2017-01-01

The presence of the Yingba (Yinggete-Bagemaode) metamorphic core complex (MCC) is confirmed near the Sino-Mongolian border in China. We report its structural evolution and the rheological features of ductile shear zones within this complex. Three deformations (Ds, Dm, and Db) since the Late Jurassic are identified. Ds is characterized by ductile structures that resulted from early NW-oriented, low-angle, extensional ductile shearing. Dm is associated with partial melting and magmatic diapirism, which accelerated the formation of the dome-like geometry of the Yingba MCC. Synchronously with or slightly subsequently to Ds and Dm, the Yingba MCC was subjected to brittle, extensional faulting (Db), which was accompanied by the exhumation of the lower crust and the formation of supracrustal basins. The ductile shearing (Ds) developed under greenschist-to amphibolite-facies metamorphic conditions (400-650 °C), as indicated by microstructures in quartz and feldspar, quartz [c] axis fabrics, and two-feldspar geothermometry. The mean kinematic vorticity estimates of 48-62% show a pure shear-preferred flow during Ds. The Yingba MCC provides an excellent sample that recorded an intermediate to high temperature shearing, which also implies the widely extensional regime in northeastern Asia at that time.

Derivation and calibration of semi-empirical gas geothermometers for Mahanagdong Geothermal Project, Philippines

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

Sanchez, D.R.

1996-12-31

The dissolved CO{sub 2}, H{sub 2}S, and H{sub 2} gases in Mahanagdong aquifer fluids are controlled by specific gas-mineral equilibria. At temperature range of 250 to 310 {degrees}C, CO{sub 2} is buffered by clinozoisite + K-feldspar + calcite + muscovite (illite) + quartz mineral assemblage. For H{sub 2}S and H{sub 2} dissolved gases, they are more likely buffered by pyrrhotite + pyrite + magnetite mineral assemblage at similar temperature range. Calibration of five Mahanagdong (MG) gas geothermometers is presented, three of which used CO{sub 2}, H{sub 2}S, and H{sub 2} concentration in steam. The remaining two use CO{sub 2}/H{sub 2}more » and H{sub 2}S/H{sub 2} ratios. The calibration is based on the relation between gas content of drillhole discharges and measured aquifer temperatures. After establishing the gas content in the aquifer, gas concentrations were computed in steam after adiabatic boiling to atmospheric condition (100 {degrees}C), to obtain gas geothermometry functions. These functions could also be used in evaluating fraction of steam condensation and temperature of phase separation. A demonstration given the Mahanagdong fumarole data, indicates that there is generally a fair relation between computed temperatures using Mahanagdong gas geothermometers and the actual field trend`s temperatures.« less

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

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

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

2014-02-01

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

A critical examination of the Emperor and Hawaiian volcanic chains

NASA Astrophysics Data System (ADS)

Nathenson, M.; Foulger, G. R.; Anderson, D. L.; Julian, B. R.; Natland, J. H.

2003-12-01

The Emperor and Hawaiian volcanic chains are usually assumed to represent a single entity, and to be an exemplary fit to the plume model. However, many features do not conform to this hypothesis. These include: 1) the great "bend" does not result from a change in direction of motion of the Pacific plate, since no such change occurred, 2) southerly motion of ~ 800 km of the melt locus occurred during formation of the Emperor chain, and stopped at the time of the great bend, 3) the chain apparently commenced near a ridge, 4) there is no Hawaiian "plume head", 5) the melt volume flux varies greatly along the chains and has increased by an order of magnitude during the last 5 Myr, 6) there is no significant heatflow anomaly around the bathymetric swell, 7) there is no measurable thermal rejuvenation near Hawaii, 8) low temperatures relative to those required for a plume are estimated from geothermometry, 9) there is no petrological or geochemical evidence that requires a deep melt source, and 10) seismic evidence indicates relatively normal wave speeds throughout the mantle beneath Hawaii. A large number of seamounts unaffiliated with volcanic chains have similar geochemistry to Hawaii. A fully quantified hypothesis for Hawaii that can explain these features is long overdue.

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

NASA Astrophysics Data System (ADS)

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

2018-03-01

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

The pre-Cainozoic basement delineation by magnetotelluric methods in the western part of the Liptovská kotlina Depression (Western Carpathians, Slovakia)

NASA Astrophysics Data System (ADS)

Fendek, Marián; Grand, Tomáš; Daniel, Slavomír; Blanárová, Veronika; Kultan, Vincent; Bielik, Miroslav

2017-08-01

The geology and hydrogeology of the Liptovská Kotlina Depression were studied by means of new geophysical methods. Controlled source audio-frequency magnetotellurics enabled us to delineate the relief of the pre-Cainozoic basement in the western part of the Liptovská Kotlina Depression into two segments with different lithostratigraphic units. Our complex findings disprove the interconnection between the Bešeňová and Lúčky water bearing structures located in the study area. The results were interpreted in the form of a resistivity cross section and resistivity model. The geological interpretation of the obtained results, taking into account the other geophysical and geological constrains showed that the pre-Cainozoic basement has a tectonically disrupted, broken relief. The Bešeňová and Lúčky structures appear to be isolated by the Palaeogene sediments (sandstone, claystone) and in the deeper part also by marly carbonates and marlstones of the Jurassic age belonging to the Fatricum. It was confirmed that the structural connectivity of geothermal aquifers in the area between the Bešeňová and Lúčky-Kaľameny should not exist. The assumption of different circulation depth was also confirmed by geothermometry and existing radiocarbon analyses applied on groundwater in both areas.

Comparative study of the silica and cation geothermometry of the Malawi hot springs: Potential alternative energy source

NASA Astrophysics Data System (ADS)

Dulanya, Zuze; Morales-Simfors, Nury; Sivertun, Åke

2010-06-01

Malawi is one of the poorest countries in the world and one of the most densely populated in south-eastern Africa. Its major power source is hydro-electricity. During the past few years, the power generation capacity has been reduced, which has impacted negatively on the socio-economic development of the country. The country holds an enormous potential to generate geothermal energy due to the country's position within the Great African Rift valley. This could contribute to economic growth, poverty reduction and technological development in Malawi. The paper presents findings of research on comparisons between silica (quartz and chalcedony) and cation geothermometers (Na-K, Na-K-Ca and K-Mg) of hot springs in the Malawi Rift, in order to deduce the temperature at depth of selected hot springs. The saturation indices of most springs have a bearing on the geology of the areas where these hot springs are found. The Na-K geothermometers are, in general, higher than the Na-K-Ca geothermometer and the K-Mg geothermometer shows temperatures that are too low to be considered. The difference in the results between the different geothermometers may indicate shallow conditions of mixing with groundwater. Results also indicate that some hot springs have sufficient heat-generating capabilities and warrant further exploration work to assess their suitability for energy generation.

Moderate-temperature zeolitic alteration in a cooling pyroclastic deposit

USGS Publications Warehouse

Levy, S.S.; O'Neil, J.R.

1989-01-01

The locally zeolitized Topopah Spring Member of the Paintbrush Tuff (13 Myr.), Yucca Mountain, Nevada, U.S.A., is part of a thick sequence of zeolitized pyroclastic units. Most of the zeolitized units are nonwelded tuffs that were altered during low-temperature diagenesis, but the distribution and textural setting of zeolite (heulandite-clinoptilolite) and smectite in the densely welded Topopah Spring tuff suggest that these hydrous minerals formed while the tuff was still cooling after pyroclastic emplacement and welding. The hydrous minerals are concentrated within a transition zone between devitrified tuff in the central part of the unit and underlying vitrophyre. Movement of liquid and convected heat along fractures from the devitrified tuff to the ritrophyre caused local devitrification and hydrous mineral crystallization. Oxygen isotope geothermometry of cogenetic quartz confirms the nondiagenetic moderate temperature origin of the hydrous minerals at temperatures of ??? 40-100??C, assuming a meteoric water source. The Topopah Spring tuff is under consideration for emplacement of a high-level nuclear waste repository. The natural rock alteration of the cooling pyroclastic deposit may be a good natural analog for repository-induced hydrothermal alteration. As a result of repository thermal loading, temperatures in the Topopah Spring vitrophyre may rise sufficiently to duplicate the inferred temperatures of natural zeolitic alteration. Heated water moving downward from the repository into the vitrophyre may contribute to new zeolitic alteration. ?? 1989.

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

NASA Astrophysics Data System (ADS)

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

2018-06-01

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

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

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

Barker, C.E.; Pawlewicz, M.J.; Bostick, N.H.

1981-01-01

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

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.

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

NASA Astrophysics Data System (ADS)

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

2018-01-01

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

Geology and geothermal potential of the tecuamburro volcano area, Guatemala

USGS Publications Warehouse

Duffield, W.A.; Heiken, G.H.; Wohletz, K.H.; Maassen, L.W.; Dengo, G.; McKee, E.H.; Castaneda, O.

1992-01-01

Tecuamburro, an andesitic stratovolcano in southeastern Guatemala, is within the chain of active volcanoes of Central America. Though Tecuamburro has no record of historic eruptions, radiocarbon ages indicate that eruption of this and three other adjacent volcanoes occurred within the past 38,300 years. The youngest eruption produced a dacite dome. Moreover, powerful steam explosions formed a 250 m wide crater about 2900 years ago near the base of this dome. The phreatic crater contains a pH-3 thermal lake. Fumaroles are common along the lake shore, and several other fumaroles are located nearby. Neutral-chloride hot springs are at lower elevations a few kilometers away. All thermal manifestations are within an area of about 400 km2 roughly centered on Tecuamburro Volcano. Thermal implications of the volume, age, and composition of the post-38.3 ka volcanic rocks suggest that magma, or recently solidified hot plutons, or both are in the crust beneath these lavas. Chemical geothermometry carried out by other workers suggests that a hydrothermal-convection system is centered over this crustal heat source. Maximum temperatures of about 300??C are calculated for samples collected in the area of youngest volcanism, whereas samples from outlying thermal manifestations yield calculated temperatures <- 165??C. An 808 m deep drill hole completed in 1990 to partly test the geothermal model developed from surface studies attained a maximum temperature of almost 240??C. Thus, the possibility of a commercial-grade hydrothermal resource in the area seems high. ?? 1992.

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.

Sapphirine-bearing granulites from the Tongbai orogen, China: Petrology, phase equilibria, zircon U-Pb geochronology and implications for Paleozoic ultrahigh temperature metamorphism

NASA Astrophysics Data System (ADS)

Xiang, Hua; Zhong, Zeng-Qiu; Li, Ye; Qi, Min; Zhou, Han-Wen; Zhang, Li; Zhang, Ze-Ming; Santosh, M.

2014-11-01

We report here for the first time the occurrence of sapphirine-bearing granulites within the Qinling Group of the Qinling-Tongbai orogen and provide robust evidence for extreme crustal metamorphism at ultrahigh-temperature (UHT) conditions. We document the UHT indicator of sapphirine and spinel in a mafic granulite consisting of orthopyroxene, biotite, plagioclase, amphibole and rutile/ilmenite. The ferromagnesian minerals in the sapphirine-bearing granulite have high XMg [Mg/(Mg + Fe)] (orthopyroxene XMg = 0.84-0.95; biotite XMg = 0.81; amphibole XMg = 0.87-0.96). The phase equilibria modeling demonstrates that the early spinel-bearing assemblage is stable at 923-950 °C and 6.7-8.9 kbar, and the peak assemblage of Opx + Pl + Spr/Spl + Amp + Bt + Ilm (+ melt) defines a field at 922-947 °C and 8.4-10.2 kbar. Rutiles have variable Zr concentrations but mostly cluster at ca. 1,500 and 3400 ppm. Zr-in-rutile geothermometry yielded high temperatures of up to 890-940 °C. Zircon U-Pb dating of the granulite constrains the timing of the immediate post-peak and retrograde metamorphic stages as 429 ± 7 Ma and 412 ± 4 Ma, respectively. The UHT metamorphism, together with extensive occurrence of coeval magmatic suites suggests that the Tongbai orogen experienced a Paleozoic Andean-type orogeny probably derived from mid-oceanic ridge subduction of the Qinling Ocean.

Origin and diagenesis of clay minerals in relation to sandstone paragenesis: An example in eolian dune reservoirs and associated rocks, Permian upper part of the Minnelusa Formation, Powder River basin, Wyoming

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

Pollastro, R.M.; Schenk, C.J.

Eolian dune sandstones are the principal reservoir rocks in the Permian upper part of the Minnelusa Formation, Powder River basin, Wyoming. These sandstones formed as shorelines retreated and dunes migrated across siliciclastic sabkhas. Sandstones are mainly quartzarenites; on average, clay minerals constitute about 5 wt.% the whole rock. Although present in minor amounts, clay minerals play an important role in the diagenetic evolution of these sandstones. Allogenic clay minerals are present in shaly rock fragments and laminae. Early infiltration of clays into porous sabkha sands commonly form characteristic menisei or bridges between framework grains or, when more extensive, form coatingsmore » or rims on grain surfaces. Authigenic clays include nearly pure smectite, mixed-layer illite/smectite (I/S), and late diagenetic illite and corrensite; these clay minerals are present as pore-lining cements. In addition to the deposition and neoformation of clay minerals throughout sandstone paragenesis, the conversion of smectite to illite occurred as temperatures increased with progressive burial. A temperature of 103C is calculated at a present depth of 3,200 m using a geothermal gradient of 30C/km and a mean annual surface temperature of 7C. After correction for uplift and erosion (250 m), the maximum calculated temperature for the conversion of all random I/S to ordered I/S is 100C. This calculated temperature is in excellent agreement with temperatures of 100-110C implied from I/S geothermometry.« less

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

USGS Publications Warehouse

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

1992-01-01

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

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.

Petrology of the 1995/2000 Magma of Copahue, Argentina

NASA Astrophysics Data System (ADS)

Goss, A.; Varekamp, J. C.

2001-05-01

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

The hydrothermal system of the Domuyo volcanic complex (Argentina): A conceptual model based on new geochemical and isotopic evidences

NASA Astrophysics Data System (ADS)

Tassi, F.; Liccioli, C.; Agusto, M.; Chiodini, G.; Vaselli, O.; Calabrese, S.; Pecoraino, G.; Tempesti, L.; Caponi, C.; Fiebig, J.; Caliro, S.; Caselli, A.

2016-12-01

The Domuyo volcanic complex (Neuquén Province, Argentina) hosts one of the most promising geothermal systems of Patagonia, giving rise to thermal manifestations discharging hot and Cl--rich fluids. This study reports a complete geochemical dataset of gas and water samples collected in three years (2013, 2014 and 2015) from the main fluid discharges of this area. The chemical and isotopic composition (δD-H2O and δ18O-H2O) of waters indicates that rainwater and snow melting are the primary recharge of a hydrothermal reservoir located at relative shallow depth (400-600 m) possibly connected to a second deeper (2-3 km) reservoir. Reactive magmatic gases are completely scrubbed by the hydrothermal aquifer(s), whereas interaction of meteoric waters at the surface causes a significant air contamination and dilution of the fluid discharges located along the creeks at the foothill of the Cerro Domuyo edifice. Thermal discharges located at relatively high altitude ( 3150 m a.s.l.), namely Bramadora, are less affected by this process, as also shown by their relatively high R/Ra values (up to 6.91) pointing to the occurrence of an actively degassing magma batch located at an unknown depth. Gas and solute geothermometry suggests equilibrium temperatures up to 220-240 °C likely referred to the shallower hydrothermal reservoir. These results, confirming the promising indications of the preliminary surveys carried out in the 1980‧s, provide useful information for a reliable estimation of the geothermal potential of this extinct volcanic system, although a detailed geophysical measurements is required for the correct estimation of depth and dimensions of the fluid reservoir(s).

Silver Peak Innovative Exploration Project (Ram Power Inc.)

DOE Data Explorer

Miller, Clay

2010-01-01

Data generated from the Silver Peak Innovative Exploration Project, in Esmeralda County, Nevada, encompasses a “deep-circulation (amagmatic)” meteoric-geothermal system circulating beneath basin-fill sediments locally blanketed with travertine in western Clayton Valley (lithium-rich brines from which have been mined for several decades). Spring- and shallow-borehole thermal-water geochemistry and geothermometry suggest that a Silver Peak geothermal reservoir is very likely to attain the temperature range 260- 300oF (~125-150oC), and may reach 300-340oF (~150-170oC) or higher (GeothermEx, Inc., 2006). Results of detailed geologic mapping, structural analysis, and conceptual modeling of the prospect (1) support the GeothermEx (op. cit.) assertion that the Silver Peak prospect has good potential for geothermal-power production; and (2) provide a theoretical geologic framework for further exploration and development of the resource. The Silver Peak prospect is situated in the transtensional (regional shearing coupled with extension) Walker Lane structural belt, and squarely within the late Miocene to Pliocene (11 Ma to ~5 Ma) Silver Peak-Lone Mountain metamorphic core complex (SPCC), a feature that accommodated initial displacement transfer between major right-lateral strike- slip fault zones on opposite sides of the Walker Lane. The SPCC consists essentially of a ductiley-deformed lower plate, or “core,” of Proterozoic metamorphic tectonites and tectonized Mesozoic granitoids separated by a regionally extensive, low-angle detachment fault from an upper plate of severely stretched and fractured structural slices of brittle, Proterozoic to Miocene-age lithologies. From a geothermal perspective, the detachment fault itself and some of the upper-plate structural sheets could function as important, if secondary, subhorizontal thermal-fluid aquifers in a Silver Peak hydrothermal system.

Silica-undersaturated reaction zones at a crust-mantle interface in the Highland Complex, Sri Lanka: Mass transfer and melt infiltration during high-temperature metasomatism

NASA Astrophysics Data System (ADS)

Fernando, G. W. A. R.; Dharmapriya, P. L.; Baumgartner, Lukas P.

2017-07-01

Sri Lanka is a crucial Gondwana fragment mostly composed of granulitic rocks in the Highland Complex surrounded by rocks with granulite to amphibolite grade in the Vijayan and Wanni Complex that were structurally juxtaposed during Pan-African orogeny. Fluids associated with granulite-facies metamorphism are thought to have controlled various lower crustal processes such as dehydration/hydration reactions, partial melting, and high-temperature metasomatism. Chemical disequilibrium in the hybrid contact zone between a near peak post-tectonic ultramafic enclave and siliceous granulitic gneiss at Rupaha within the Highland Complex produced metasomatic reaction zones under the presence of melt. Different reaction zones observed in the contact zone show the mineral assemblages phlogopite + spinel + sapphirine (zone A), spinel + sapphirine + corundum (zone B), corundum ( 30%) + biotite + plagioclase zone (zone C) and plagioclase + biotite + corundum ( 5%) zone (zone D). Chemical potential diagrams and mass balance reveal that the addition of Mg from ultramafic rocks and removal of Si from siliceous granulitic gneiss gave rise to residual enrichment of Al in the metasomatized mineral assemblages. We propose that contact metasomatism between the two units, promoted by melt influx, caused steady state diffusional transport across the profile. Corundum growth was promoted by the strong residual Al enrichment and Si depletion in reaction zone whereas sapphirine may have been formed under high Mg activity near the ultramafic rocks. Modelling also indicated that metasomatic alteration occurred at ca. 850 °C at 9 kbar, which is consistent with post-peak metamorphic conditions reached during the initial stage of exhumation in the lower crust and with temperature calculations based on conventional geothermometry.

Low-temperature geothermal potential of the Ojo Caliente warm springs area, northern New Mexico

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

Vuataz, F.D.; Stix, J.; Goff, F.

1984-05-01

A detailed geochemical investigation of 17 waters (thermal and cold, mineralized and dilute) was performed in the Ojo Caliente-La Madera area. Two types of thermomineral waters have separate and distinctive geologic, geochemical, and geothermal characteristics. The water from Ojo Caliente Resort emerges with temperatures less than or equal to 54/sup 0/C from a Precambrian metarhyolite. Its chemistry, typically Na-HCO/sub 3/, has a total mineralization of 3600 mg/l. Isotopic studies have shown that the thermal water emerges from the springs and a hot well without significant mixing with the cold shallow aquifer of the valley alluvium. However, the cold aquifer adjacentmore » to the resort does contain varying amounts of thermal water that originates from the warm spring system. Geothermometry calculations indicate that the thermal water may be as hot as 85/sup 0/C at depth before its ascent toward surface. Thermodynamic computations on the reaction states of numerous mineral phases suggest that the thermal water will not cause major scaling problems if the hot water is utilized for direct-use geothermal applications. By means of a network of very shallow holes, temperature and electrical conductivity anomalies have been found elsewhere in the valley around Ojo Caliente, and resistivity soundings have confirmed the presence of a plume of thermal water entering the shallow aquifer. The group of lukewarm springs around La Madera, with temperatures less than or equal to 29/sup 0/C, chemical type of NaCaMg-HCO/sub 3/Cl and with a total mineralization less than or equal to 1500 mg/l behaves as a different system without any apparent relation to the Ojo Caliente system. Its temperature at depth is not believed to exceed 35 to 40/sup 0/C.« less

Idetification of the chemical sedimentary protolish of the early Paleoproterozoic banded iron formation from Wuyang area, in the southern margin of the North China Craton

NASA Astrophysics Data System (ADS)

Lan, C.; Zhao, T.

2016-12-01

The Paleoproterozoic banded iron formation (BIF) from Wuyang area in the southern margin of the North China Craton (NCC) were metamorphosed under granulite facies, and are characterized with an assemblage of clinopyroxene, magnetite and orthopyroxene. Two types of iron ores can be identified on the basis of macro- and micro-textures: banded quartz-clinopyroxene (±othopyroxene) -magnetite ores and massive clinopyroxene-magnetite ores. Two-pyroxene geothermometry indicates that the primary counterparts of these ores have undergone metamorphism with a peak temperature of about 762±9°. Both the banded and massive ores have also similarly BIF-like REE+Y features, and thus are proposed to have all formed from chemical sediments. Similarly, clinopyroxenes from both types have BIF-like rare earth element compositions and are rich in Fe (16-23 wt.% FeOtotoal), further suggesting that they are primary Fe-Mg-Ca-rich chemical sediments during metamorphism. Slight enrichments of TiO2, Al2O3, Zr, Hf, Ta and Th of the Wuyang IF suggest relatively low detritus input. The massive ore have magnetite containing V, Cr and Ti much higher than those of the banded ores, suggesting that they may have undergone stronger secondary alteration possibly related to the intrusion of nearby pyroxenite plutons. Different ores have seawater-like REE+Y patterns with LREE depletions and positive anomalies of La, Eu, and Y, showing that granulite facies metamorphism did not essentially modify the primary compositions of the Wuyang IF deposited from paleo-seawater. Our results suggest less than 0.1% contribution from high-temperature hydrothermal fluids.

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

NASA Astrophysics Data System (ADS)

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

2016-12-01

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

Recent exploration and development of geothermal energy resources in the Escalante desert region, Southwestern Utah

USGS Publications Warehouse

Blackett, Robert E.; Ross, Howard P.

1994-01-01

Development of geothermal resources in southwest Utah's Sevier thermal area continued in the early 1990s with expansion of existing power-generation facilities. Completion of the Bud L. Bonnett geothermal power plant at the Cove Fort-Sulphurdale geothermal area brought total power generation capacity of the facility to 13.5 MWe (gross). At Cove Fort-Sulphurdate, recent declines in steam pressures within the shallow, vapor-dominated part of the resource prompted field developers to complete additional geothermal supply wells into the deeper, liquid-dominated portion of the resource. At Roosevelt Hot Springs near Milford, Intermountain Geothermal Company completed an additional supply well for Utah Power and Light Company's single-flash, Blundell plant. with the increased geothermal fluid supply from the new well, the Blundell plant now produces about 26 MWe (gross). The authors conducted several geothermal resource studies in undeveloped thermal areas in southwest Utah. Previous studies at Newcastle revealed a well-defined, self-potential minimum coincident with the intersection of major faults and the center of the heatflow anomaly. A detailed self-potential survey at Wood's Ranch, an area in northwest Iron County where thermal water was encountered in shallow wells, revealed a large (5,900 ?? 2,950 feet [1,800 ?? 900 m]) northeast-oriented self-potential anomaly which possibly results from the flow of shallow thermal fluid. Chemical geothermometry applied to Wood's Ranch water samples suggest reservoir temperatures between 230 and 248??F (110 and 120??C). At the Thermo Hot Springs geothermal area near Minersville, detailed self-potential surveys have also revealed an interesting 100 mV negative anomaly possibly related to the upward flow of hydrothermal fluid.

The effect of water on recrystallization behavior and grain boundary morphology in calcite observations of natural marble mylonites

NASA Astrophysics Data System (ADS)

Schenk, Oliver; Urai, Janos L.; Evans, Brian

2005-10-01

Fluids are inferred to play a major role in the deformation and recrystallization of many minerals (e.g. quartz, olivine, halite, feldspar). In this study, we sought to identify the effect of fluids on grain boundary morphology and recrystallization processes in marble mylonites during shear zone evolution. We compared the chemistry, microstructure and mesostructure of calcite marble mylonites from the Schneeberg Complex, Southern Tyrole, Italy, to that from the Naxos Metamorphic Core Complex, Greece. These two areas were selected for comparison because they have similar lithology and resemble each other in chemical composition. In addition, calcite-dolomite geothermometry indicates similar temperatures for shear zone formation: 279±25 °C (Schneeberg Complex) and 271±15 °C (Naxos high-grade core). However, the two settings are different in the nature of the fluids present during the shear zone evolution. In the Schneeberg mylonites, both the alteration of minerals during retrograde metamorphism in the neighboring micaschists and the existence of veins suggest that aqueous fluids were present during mylonitization. The absence of these features in the Naxos samples indicates that aqueous fluids were not as prevalent during deformation. This conclusion is also supported by the stable isotope signature. Observations of broken and planar surfaces using optical and scanning electron microscopes did not indicate major differences between the two mylonites: grain boundaries in both settings display pores with shapes controlled by crystallography, and have pore morphologies that are similar to observations from crack and grain-boundary healing experiments. Grain size reduction was predominantly the result of subgrain rotation recrystallization. However, the coarse grains inside the wet protomylonites (Schneeberg) are characterized by intracrystalline shear zones.

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.

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

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

Moran, James J.; Whitmore, Laura M.; Jay, Zackary J.

Volcanism and post-magmatism contribute both significant annual CH 4 fluxes to the atmosphere (on par with other natural sources such as forest fire and wild animal emissions) and have been implicated in past climate-change events. The Yellowstone hot spot is one of the largest volcanic systems on Earth and is known to emit methane in addition to other greenhouse gases (e.g. carbon dioxide) but the ultimate source of this methane flux has not been elucidated. Here we use dual stable isotope analysis (δ 2H and δ 13C) of CH 4(g) sampled from ten high-temperature geothermal pools in Yellowstone National Parkmore » to show that the predominant flux of CH4(g) is abiotic. The average δ 13C and δ 2H values of CH 4(g) emitted from hot springs (-26.7 (±2.4) and -236.9 (±12.0) ‰, respectively) are not consistent with biotic (microbial or thermogenic) methane sources, but are within previously reported ranges for abiotic methane production. Correlation between δ 13C CH4 and δ 13C-dissolved inorganic C (DIC) also suggests that CO 2 is a parent C source for the observed CH 4(g). Moreover, CH 4-CO 2 isotopic geothermometry was used to estimate CH 4(g) formation temperatures ranging from ~ 250 - 350°C, which is just below the temperature estimated for the hydrothermal reservoir and consistent with the hypothesis that subsurface, rock-water interactions are responsible for large methane fluxes from this volcanic system. An understanding of conditions leading to the abiotic production of methane and associated isotopic signatures are central to understanding the evolutionary history of deep carbon sources on Earth.« less

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

NASA Astrophysics Data System (ADS)

Hardwick, C.; Kirby, S.

2014-12-01

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

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.

Updating of the geological and geothermal research on Milos island

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

Fytikas, M.

1989-01-01

The oldest geologic formations outcropping in Milos are an Alpine age crystalline basement and a transgressive marine Neogene sequence. The island is mainly volcanic. It belongs to the Aegean Active Arc, within which the Milos archipelago shows the most important volcanism in terms of quantity, variety of products and duration of activity (3.5-0.8 M.a.). There are no large central volcanic edifices but different, frequently coeval eruption centres. The initial and intermediate phases of activity were mainly pyroclastic and submarine, whereas the last one (0.1 M.a.) was subaerial and formed tuff rings, surge deposits and lava flows, all of homogenous rhyoliticmore » composition. Recent detailed studies have addressed the mechanism of feeding and the type of magmatic chambers beneath Milos. Distention tectonics have two main phases: an earlier one (Pliocene) with NE-SW direction and a much more intense recent (Quaternary) one, trending NW-SE. The geological, tectonic and magmatic activity favoured the formation of a high enthalpy geothermal field. Many fossil and active thermal manifestations exist: hot springs, fumaroles, hot grounds, phreatic explosion craters. The hydrothermal alteration of the volcanites produced, by self sealing, a perfect cover for the geothermal fluids. Geothermometry of the surface fluids indicated high values for the source temperatures and very high geothermal gradients in central and eastern Milos. Geothermally anomalous zones, defined by two different methods, together with superficial geological and tectonic information, permitted the location of sites for deep drilling. Five exploratory wells 1000-1400m deep gave satisfactory results of flow rate (40-120 t/h), temperature (300-320{sup 0}C) and enthalpy.« less

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

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

Stockli, Daniel F.

2015-11-30

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

Ti-in-biotite geothermometry in non-graphitic, peraluminous metapelites from Crni vrh and Resavski humovi (Central Serbia)

NASA Astrophysics Data System (ADS)

Erić, Suzana; Logar, Mihovil; Milovanović, Dragan; Babič, Danilo; Adnađević, Borivoj

2009-02-01

The study discusses the application of the Ti-in-biotite geothermometer of Henry et al. (2005) to the example of biotites from non-graphitic peraluminous micaschists of Central Serbia. Three petrographically different micaschists were distinguished on the basis of the following mineral assemblages: CV1 (St-Grt-Bt-Ms-Pg-Pl-Qtz), CV2 (Grt-St-Ky-Bt-Ms-Pl-Qtz) and RH (Grt-St-Bt-Ms-Pl-Qtz). Applying different geothermobarometers it was estimated that the studied micaschists were metamorphosed at average temperatures and pressures of 530 °C and 520 MPa (CV1incl), 580 °C and 670 MPa (CV1), 630 °C and 700 MPa (CV2) and 550 °C, 680 MPa (RH). The average temperatures obtained by the Ti-in-biotite method revealed uniform values for CV1 and CV2 micaschists and these values are very similar to the temperatures obtained by other methods. In contrast, the application of Ti-in-biotite geothermometer for RH micaschist yields the temperature difference of 85-110 °C. The variability of temperature is interpreted as a result of a positive correlation of Ti contents and XMg values in RH biotite, which is in disagreement with the principles of the Ti-in-biotite method. The positive Ti-XMg correlation is a result of the compositional variability shown by RH biotites from different samples, which can possibly be related to compositional inhomogeneities of the pelitic protolith. On the other hand, the Ti-in-biotite geothermometer for CV2 biotite gave very uniform temperatures despite variable Ti contents (Ti = 0.260, sd = 0.018 apfu). This is explained as result of the low sensitivity of Ti-in-biotite geothermometer for high Ti concentrations (> 0.25 apfu).

Microstructural, textural and thermal evolution of an exhumed strike-slip fault and insights into localization and rheological transition

NASA Astrophysics Data System (ADS)

Cao, Shuyun; Neubauer, Franz; Liu, Junlai; Bernroider, Manfred; Genser, Johann

2016-04-01

The presence of deep exhumed crustal rocks with a dominant but contrasting mineralogy results in shear concentration in the rheological weakest layer, which exhibits contrasting patterns of fabrics and thermal conditions during their formation. We tested a combination of methodologies including microstructural and textural investigations, geochronology and geothermometry on deformed rocks from exhumed strike-slip fault, Ailao Shan-Red River, SE, Asian. Results indicate that the exhumed deep crustal rocks since late Oligocene (ca. 28 Ma) to Pliocene (ca. 4 Ma) typically involve dynamic microstructural, textural and thermal evolution processes, which typically record a progressive deformation and syn-kinematic reactions from ductile to semi-ductile and brittle behavior during exhumation. This transformation also resulted in dramatic strength reduction that promoted strain localization along the strike-slip and transtensional faults. Detailed analysis has revealed the co-existence of microfabrics ranging from high-temperatures (granulite facies conditions) to overprinting low-temperatures (lower greenschist facies conditions). The high-temperature microstructures and textures are in part or entirely altered by subsequent, overprinting low-temperature shearing. In quartz-rich rocks, quartz was deformed in the dislocation creep regime and records transition of microfabrics and slip systems during decreasing temperature, which lasted until retrogression related to final exhumation. As a result, grain-size reduction associated by fluids circulating within the strike-slip fault zone at brittle-ductile transition leads to rock softening, which resulted in strain localization, weak rock rheology and the overall hot thermal structure of the crust. Decompression occurred during shearing and as a result of tectonic exhumation. All these results demonstrate that the ductile to ductile-brittle transition involves a combination of different deformation mechanisms, rheological transition features and feedbacks between deformation, decreasing temperature and fluids.

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

NASA Astrophysics Data System (ADS)

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

2009-12-01

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

Origin of ultramafic xenoliths containing exsolved pyroxenes from Hualalai Volcano, Hawaii

USGS Publications Warehouse

Bohrson, W.A.; Clague, D.A.

1988-01-01

Hualalai Volcano, Hawaii, is best known for the abundant and varied xenoliths included in the historic 1800 Kaupulehu alkalic basalt flow. Xenoliths, which range in composition from dunite to anorthosite, are concentrated at 915-m elevation in the flow. Rare cumulate ultramafic xenoliths, which include websterite, olivine websterite, wehrlite, and clinopyroxenite, display complex pyroxene exsolution textures that indicate slow cooling. Websterite, olivine websterite, and one wehrlite are spinel-bearing orthopyroxene +olivine cumulates with intercumulus clinopyroxene +plagioclase. Two wehrlite samples and clinopyroxenite are spinel-bearing olivine cumulates with intercumulus clinopyroxene+orthopyroxene + plagioclase. Two-pyroxene geothermometry calculations, based on reconstructed pyroxene compositions, indicate that crystallization temperatures range from 1225?? to 1350?? C. Migration or unmixing of clinopyroxene and orthopyroxene stopped between 1045?? and 1090?? C. Comparisons of the abundance of K2O in plagioclase and the abundances of TiO2 and Fe2O3in spinel of xenoliths and mid-ocean ridge basalt, and a single 87Sr/ 86Sr determination, indicate that these Hualalai xenoliths are unrelated to mid-ocean ridge basalt. Similarity between the crystallization sequence of these xenoliths and the experimental crystallization sequence of a Hawaiian olivine tholeiite suggest that the parental magma of the xenoliths is Hualalai tholeiitic basalt. Xenoliths probably crystallized between about 4.5 and 9 kb. The 155??-230?? C of cooling which took place over about 120 ka - the age of the youngest Hualalai tholeiitic basalt - yield maximum cooling rates of 1.3??10-3-1.91??10-3 ??C/yr. Hualalai ultramafic xenoliths with exsolved pyroxenes crystallized from Hualalai tholeiitic basalt and accumulated in a magma reservoir located between 13 and 28 km below sealevel. We suspect that this reservoir occurs just below the base of the oceanic crust at about 19 km below sealevel. ?? 1988 Springer-Verlag.

13C 12C exchange between calcite and graphite: A possible thermometer in Grenville marbles

USGS Publications Warehouse

Valley, J.W.; O'Neil, J.R.

1981-01-01

The fractionation of 13C between calcite and graphite, ??(Cc-Gr). is consistently small (2.6-4.8 permil) in 34 assemblages from upper amphibolite- and granulite-facies marbles of the Grenville Province. In 25 samples from the Adirondack Mountains, New York, it decreases regularly with increasing metamorphic temperature. The fractionations are independent of absolute ??13C values of calcite (-2.9 to +5.0). For T = 600-800??C, the Adirondack data are described by ??(Cc-Gr) = -0.00748T (??C) + 8.68. This good correlation between ?? and T suggests that carbon isotope equilibrium was attained in these high-grade marbles and that the theoretical calculations of this fractionation by Bottinga are approximately 2 permil too large in this temperature range. Because of the relatively high temperature sensitivity suggested by these results and by Bottinga's calculations, and the pressure independence of isotope fractionation, ??(Cc-Gr) may provide a very good thermometer for high-grade marbles. Comparison of this field calibration for ??(Cc-Gr) vs temperature with results from other terranes supports the utility of ??(Cc-Gr) for geothermometry and suggests that graphite is much more sluggish to exchange than calcite, that exchange between calcite and graphite occurs at temperatures as low as 300??C, and that equilibrium may normally be attained only when peak metamorphic temperatures are greater than 500-600??C. Because 13C exchange is an unavoidable metamorphic process at temperatures above 300??C, high values of ??13C(Gr) in moderate- to high-grade carbonate-bearing rocks do not provide a sufficient criterion to infer an abiogenic origin for the graphite. ?? 1981.

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.

Strength of the Subduction Plate Interface beneath the Seismogenic Zone: A Microstructural Investigation of Deformation Mechanisms within a Phyllosilicate- and Amphibole-rich Shear Zone

NASA Astrophysics Data System (ADS)

Seyler, C.; Kirkpatrick, J. D.; Šilerová, D.

2017-12-01

Localization of strain at plate boundaries requires rheological weakening of the lithosphere. The rheology of the subduction plate interface is dictated by the dominant grain-scale deformation mechanisms. However, little is known about the deformation mechanisms within phases commonly found in subduction zones, such as phyllosilicates and amphiboles. We investigate the Leech River Shear Zone on Vancouver Island, British Columbia to explore deformation processes downdip of the seismogenic zone and evaluate the bulk rheology of the plate interface. This shear zone juxtaposes a metamorphosed accretionary prism against a metabasaltic oceanic plateau, representing a paleo-plate interface from the ancient Cascadia subduction zone. Preliminary geothermometry results record a prograde deformation temperature of 573.6±11.2 ˚C in the overriding accretionary wedge, and the hornblende-chlorite-epidote-plagioclase mineral assemblage suggests upper greenschist to lower amphibolite facies metamorphism of the downgoing oceanic crust. Detailed mapping of the plate interface documents a 200 m wide mylonitic shear zone developed across the lithologic contact. Asymmetric shear fabrics, isoclinal folding, boudinage, and a steeply plunging, penetrative stretching lineation are consistent with sinistral-oblique subduction. Numerous discordant quartz veins are variably sheared into sigmoidal shapes as well as isoclinally folded and boudinaged, indicating cyclical synkinematic fracture and vein formation. At the grain-scale, interconnected, anastomosing layers of muscovite, chlorite, and graphite in the accretionary prism rocks likely deformed through kinking and dislocation glide. Framework minerals such as quartz and feldspar deformed by dislocation creep. In the metabasalt, hornblende and chlorite form a continuous S—C fabric in which asymmetric hornblende porphyroclasts deformed by rigid grain rotation and dissolution-precipitation creep. The strength of the subduction plate interface beneath the seismogenic zone was therefore controlled by multiple syn-kinematic mechanisms, with overall strength dominated by the rheology of phyllosilicates and amphibole, generating very low viscosities at the plate interface and enhancing strain localization.

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

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

Ghanashayam Neupane; Earl D. Mattson; Cody J. Cannon

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

Synthesis of monticellite-forsterite and merwinite-forsterite symplectites in the CaO-MgO-SiO2 model system: influence of temperature and water content on microstructure evolution

NASA Astrophysics Data System (ADS)

Remmert, P.; Heinrich, W.; Wunder, B.; Morales, L.; Wirth, R.; Rhede, D.; Abart, R.

2018-01-01

Homogeneous single crystals of synthetic monticellite with the composition {Ca}_{0.88}{Mg}_{1.12}{SiO}_4 (Mtc I) were annealed in a piston-cylinder apparatus at temperatures between 1000 and 1200°C, pressures of 1.0-1.4 GPa, for run durations from 10 min to 24 h and applying bulk water contents ranging from 0.0 to 0.5 wt% of the total charge. At these conditions, Mtc I breaks down to a fine-grained, symplectic intergrowth. Thereby, two types of symplectites are produced: a first symplectite type (Sy I) is represented by an aggregate of rod-shaped forsterite immersed in a matrix of monticellite with end-member composition (Mtc II), and a second symplectite type (Sy II) takes the form of a lamellar merwinite-forsterite intergrowth. Both symplectites may form simultaneously, where the formation of Sy I is favoured by the presence of water. Sy I is metastable with respect to Sy II and is successively replaced by the latter. For both symplectite types, the characteristic spacing of the symplectite phases is independent of run duration and is only weeakly influenced by the water content, but it is strongly temperature dependent. It varies from about 400 nm at 1000°C to 1200 nm at 1100°C in Sy I, and from 300 nm at 1000°C to 700 nm at 1200°C in Sy II. A thermodynamic analysis reveals that the temperature dependence of the characteristic spacing of the symplectite phases is due to a relatively high activation energy for chemical segregation by diffusion within the reaction front as compared to the activation energy for interface reactions at the reaction front. The temperature dependence of the characteristic lamellar spacing and the temperature-time dependence of overall reaction progress have potential for applications in geo-thermometry and geo-speedometry.

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.

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.

Recent volcanic history of Irazu volcano, Costa Rica: alternation and mixing of two magma batches, and pervasive mixing

USGS Publications Warehouse

Alvarado, Guillermo E.; Carr, Michael J.; Turrin, Brent D.; Swisher, Carl C.; Schmincke, Hans-Ulrich; Hudnut, Kenneth W.

2006-01-01

40Ar/39Ar dates, field observations, and geochemical data are reported for Irazú volcano, Costa Rica. Volcanism dates back to at least 854 ka, but has been episodic with lava shield construction peaks at ca. 570 ka and 136–0 ka. The recent volcanic record on Irazú volcano comprises lava flows and a variety of Strombolian and phreatomagmatic deposits, with a long-term trend toward more hydrovolcanic deposits. Banded scorias and hybridized rocks reflect ubiquitous magma mixing and commingling. Two distinct magma batches have been identified. One magma type or batch, Haya, includes basalt with higher high field strength (HFS) and rare-earth element contents, suggesting a lower degree melt of a subduction modified mantle source. The second batch, Sapper, has greater enrichment of large ion lithophile elements (LILE) relative to HFS elements and rare-earth elements, suggesting a higher subduction signature. The recent volcanic history at Irazú records two and one half sequences of the following pattern: eruptions of the Haya batch; eruptions of the Sapper batch; and finally, an unusually clear unconformity, indicating a pause in eruptions. In the last two sequences, strongly hybridized magma erupted after the eruption of the Haya batch. The continuing presence of two distinct magma batches requires two active magma chambers. The common occurrence of hybrids is evidence for a small, nearer to the surface chamber for mixing the two batches. Estimated pre-eruptive temperatures based on two-pyroxene geothermometry range from ∼1000–1176 °C in basalts to 922 °C in hornblende andesites. Crystallization occurred mainly between 4.6 and 3 kb as measured by different geobarometers. Hybridized rocks show intermediate pressures and temperatures. High silica magma occurs in very small volumes as banded scorias but not as lava flows. Although eruptions at Irazú are not often very explosive, the pervasiveness of magma mixing presents the danger of larger, more explosive hybrid eruptions.

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.

Origin of ultramafic xenoliths containing exsolved pyroxenes from Hualalai Volcano, Hawaii

NASA Astrophysics Data System (ADS)

Bohrson, Wendy A.; Clague, David A.

1988-10-01

Hualalai Volcano, Hawaii, is best known for the abundant and varied xenoliths included in the historic 1800 Kaupulehu alkalic basalt flow. Xenoliths, which range in composition from dunite to anorthosite, are concentrated at 915-m elevation in the flow. Rare cumulate ultramafic xenoliths, which include websterite, olivine websterite, wehrlite, and clinopyroxenite, display complex pyroxene exsolution textures that indicate slow cooling. Websterite, olivine websterite, and one wehrlite are spinel-bearing orthopyroxene +olivine cumulates with intercumulus clinopyroxene +plagioclase. Two wehrlite samples and clinopyroxenite are spinel-bearing olivine cumulates with intercumulus clinopyroxene+orthopyroxene + plagioclase. Two-pyroxene geothermometry calculations, based on reconstructed pyroxene compositions, indicate that crystallization temperatures range from 1225° to 1350° C. Migration or unmixing of clinopyroxene and orthopyroxene stopped between 1045° and 1090° C. Comparisons of the abundance of K2O in plagioclase and the abundances of TiO2 and Fe2O3in spinel of xenoliths and mid-ocean ridge basalt, and a single 87Sr/ 86Sr determination, indicate that these Hualalai xenoliths are unrelated to mid-ocean ridge basalt. Similarity between the crystallization sequence of these xenoliths and the experimental crystallization sequence of a Hawaiian olivine tholeiite suggest that the parental magma of the xenoliths is Hualalai tholeiitic basalt. Xenoliths probably crystallized between about 4.5 and 9 kb. The 155° 230° C of cooling which took place over about 120 ka — the age of the youngest Hualalai tholeiitic basalt — yield maximum cooling rates of 1.3×10-3 1.91×10-3 °C/yr. Hualalai ultramafic xenoliths with exsolved pyroxenes crystallized from Hualalai tholeiitic basalt and accumulated in a magma reservoir located between 13 and 28 km below sealevel. We suspect that this reservoir occurs just below the base of the oceanic crust at about 19 km below sealevel.

Relict chondrules in primitive achondrites: Remnants from their precursor parent bodies

NASA Astrophysics Data System (ADS)

Schrader, Devin L.; McCoy, Timothy J.; Gardner-Vandy, Kathryn

2017-05-01

We studied the petrography, analyzed the chemical compositions, constrained the closure temperatures (via geothermometry), and determined the oxidation states of relict chondrules in Campo del Cielo (IAB iron meteorite), Graves Nunataks (GRA) 98028 (acapulcoite), and Netschaëvo (IIE iron meteorite) to constrain their formation conditions and investigate links to known meteorite groups. Despite having been thermally metamorphosed, mineral phases within relict chondrules retain information about their precursor compositions. The sizes and textures of relict chondrules, and silicate and chromite compositions indicate that Campo del Cielo, GRA 98028, and Netschaëvo had distinct parent bodies that were similar to, but different from, known chondrite groups. To determine the utility of relict chondrule sizes in thermally metamorphosed meteorites, we determined the chondrule size distributions in the LL chondrites Semarkona (LL3.00), Soko-Banja (LL4), Siena (LL5), and Saint-Séverin (LL6), and the H chondrites Clovis (No. 1) (H3.6), Kesen (H4), Arbol Solo (H5), and Estacado (H6). As expected, mean chondrule diameters increase with degree of thermal metamorphism. We find that Campo del Cielo and GRA 98028 were reduced during thermal metamorphism, consistent with previous studies, indicating that their precursors were initially more FeO-rich than their current compositions. In contrast to previous studies, we find no evidence for reduction of silicates in Netschaëvo. Normal zoning of olivine in Netschaëvo is consistent with crystallization and suggests its silicates are near their primary FeO-contents. The presence of elongated chromite grains along olivine grain boundaries in Netschaëvo indicates formation during thermal metamorphism under oxidizing conditions. Due to the absence of reduction and the composition of chromite being distinct from that of metamorphosed H chondrites, we conclude that Netschaëvo, and by extension the IIE iron meteorites, are not from the H chondrite parent body.

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

NASA Astrophysics Data System (ADS)

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

2010-11-01

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

Structures, microfabrics and textures of the Cordilleran-type Rechnitz metamorphic core complex, Eastern Alps☆

PubMed Central

Cao, Shuyun; Neubauer, Franz; Bernroider, Manfred; Liu, Junlai; Genser, Johann

2013-01-01

Rechnitz window group represents a Cordilleran-style metamorphic core complex, which is almost entirely located within nearly contemporaneous Neogene sediments at the transition zone between the Eastern Alps and the Neogene Pannonian basin. Two tectonic units are distinguished within the Rechnitz metamorphic core complex (RMCC): (1) a lower unit mainly composed of Mesozoic metasediments, and (2) an upper unit mainly composed of ophiolite remnants. Both units are metamorphosed within greenschist facies conditions during earliest Miocene followed by exhumation and cooling. The internal structure of the RMCC is characterized by the following succession of structure-forming events: (1) blueschist relics of Paleocene/Eocene age formed as a result of subduction (D1), (2) ductile nappe stacking (D2) of an ophiolite nappe over a distant passive margin succession (ca. E–W to WNW–ESE oriented stretching lineation), (3) greenschist facies-grade metamorphism annealing dominant in the lower unit, and (4) ductile low-angle normal faulting (D3) (with mainly NE–SW oriented stretching lineation), and (5) ca. E to NE-vergent folding (D4). The microfabrics are related to mostly ductile nappe stacking to ductile low-angle normal faulting. Paleopiezometry in conjunction with P–T estimates yield high strain rates of 10− 11 to 10− 13 s− 1, depending on the temperature (400–350 °C) and choice of piezometer and flow law calibration. Progressive microstructures and texture analysis indicate an overprint of the high-temperature fabrics (D2) by the low-temperature deformation (D3). Phengitic mica from the Paleocene/Eocene high-pressure metamorphism remained stable during D2 ductile deformation as well as preserved within late stages of final sub-greenschist facies shearing. Chlorite geothermometry yields two temperature groups, 376–328 °C, and 306–132 °C. Chlorite is seemingly accessible to late-stage resetting. The RMCC underwent an earlier large-scale coaxial deformation accommodated by a late non-coaxial shear with ductile low-angle normal faulting, resulting in subvertical thinning in the extensional deformation regime. The RMCC was rapidly exhumed during ca. 23–18 Ma. PMID:27065502

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

NASA Astrophysics Data System (ADS)

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

2017-12-01

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

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.

Basanite-nephelinite suite from early Kilauea: Carbonated melts of phlogopite-garnet peridotite at Hawaii's leading magmatic edge

USGS Publications Warehouse

Sisson, T.W.; Kimura, Jun-Ichi; Coombs, M.L.

2009-01-01

A basanite-nephelinite glass suite from early submarine Kilauea defines a continuous compositional array marked by increasing concentrations of incompatible components with decreasing SiO2, MgO, and Al2O3. Like peripheral and post-shield strongly alkalic Hawaiian localities (Clague et al. in J Volcanol Geotherm Res 151:279-307, 2006; Dixon et al. in J Pet 38:911-939, 1997), the early Kilauea basanite-nephelinite glasses are interpreted as olivine fractionation products from primary magnesian alkalic liquids. For early Kilauea, these were saturated with a garnet-phlogopite-sulfide peridotite assemblage, with elevated dissolved CO2 contents responsible for the liquids' distinctly low-SiO2 concentrations. Reconstructed primitive liquids for early Kilauea and other Hawaiian strongly alkalic localities are similar to experimental 3 GPa low-degree melts of moderately carbonated garnet lherzolite, and estimated parent magma temperatures of 1,350-1,400??C (olivine-liquid geothermometry) match the ambient upper mantle geotherm shortly beneath the base of the lithosphere. The ???3 GPa source regions were too hot for stable crystalline carbonate and may have consisted of ambient upper mantle peridotite containing interstitial carbonate-silicate or carbonatitic liquid, possibly (Dixon et al. in Geochem Geophys Geosyst 9(9):Q09005, 2008), although not necessarily, from the Hawaiian mantle plume. Carbonate-enriched domains were particularly susceptible to further melting upon modest decompression during upward lithospheric flexure beneath the advancing Hawaiian Arch, or by conductive heating or upward drag by the Hawaiian mantle plume. The early Kilauea basanite-nephelinite suite has a HIMU-influenced isotopic character unlike other Hawaiian magmas (Shimizu et al. in EOS Tran Amer Geophys Union 82(47): abstr V12B-0962, 2001; Shimizu et al. in Geochim Cosmochim Acta 66(15A):710, 2002) but consistent with oceanic carbonatite involvement (Hoernle et al. in Contrib Mineral Petrol 142:520-542, 2002). It may represent the melting products of a fertile domain in the ambient upper mantle impinged upon and perturbed by the sustained plume source that feeds later shield-stage magmatism. ?? US Government 2009.

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.

Tectonothermal evolution of the Triassic flysch in the Bayan Har Orogen, Tibetan plateau

NASA Astrophysics Data System (ADS)

Wang, Hejing; Rahn, Meinert; Zhou, Jian

2018-01-01

The Bayan Har Orogen comprises a major part of the "Qingzang-Dianxi fold region" in western China. It preserves important information of the tectono-thermal evolution covering the time span from the closure of the Paleo-Tethys Ocean up to the formation of the Himalayas. Low temperature metamorphic indicators, such as mineral assemblages, illite "crystallinity" (IC), chlorite "crystallinity" (CC), illite polytype, b-cell dimension of K-white micas, geothermometry of selected minerals were analyzed. The values of Kübler index (KI) of the Triassic flysch in the Bayan Har Orogen range from 0.23-1.63°Δ2θ while Árkai index (ÁI) in a range of 0.21-0.60°Δ2θ. Iso-thermal zones mapped with KI describe a pair of anchizones and an anchiregion within the Bayan Har Orogen: the "Giant Yushu Anchizone" in the southwest (extending > 750 km long and 100 km wide), the "Zaling-Eling-Lakes Anchizone" in the center (about 150 km long and 40 km wide) and the "Xing-Tong-Zhe Anchiregion" in the northeast (covering an area of roughly 60,000 km2). They are separated by diagenetic zones. Peak metamorphic conditions are estimated around 280-330 °C and a low to intermediate (N. New Hampshire) pressure type. A slight change with increasing then decreasing pressure was observed from SW to NE. The relationship between anchimetamorphic pattern of Triassic flysch and large-scale folds and faults indicates syn- to post structural metamorphism. Compression at the end of the Triassic, induced by the interaction of the Tarim, North China and Indian blocks caused the closure of the Paleo-Tethys Ocean and led to the folding of the Triassic flysch within the Paleo-Tethys Ocean basin. Anchimetamorphism may have been caused by crustal thickening of > 10 km due to an accretionary wedge setting and a temperature increase in those rocks due to burial. Such a regional metamorphic pattern would provide important information for reconstruction of palaeotectonic-palaeogeograph and the evolutionary history of Tibetan plateau.

Fluid evolution of Au-Cu zones in Um Balad area, North Eastern Desert of Egypt: Implications from mineral chemistry and fluid inclusions

NASA Astrophysics Data System (ADS)

Abd El Monsef, Mohamed; Salem, Ibrahim; Slobodník, Marek; Ragab, Ahmed

2018-07-01

Scanning electron microscope (SEM), Electron microprobe (EMPA) and fluid inclusion studies of the ore body, as well as geochemical analyses of country rocks were performed to determine the nature and characteristics of the mineralizing fluid responsible for Au-Cu deposits in Um Balad area, Northern Eastern Desert of Egypt. The Um Balad Au-Cu deposits are confined to well developed-quartz veins and veinlets cutting through the hosting country rocks. Petrographic and geochemical investigations of the hosting rocks distinguished between two main rock units; 1) metagabbro-diorite rocks with tholeiitic nature derived in island arc/continental margin tectonic regime, and 2) granodiorite rocks formed from calc-alkaline magma in continental margin regime. Wallrock alterations are represented by propylitic and argillic types. The mineralized quartz veins are striking in NE-SW direction and dipping between (35°-45°) in SE direction, other mineralized mafic dykes enriched with auriferous quartz veinlets are trending NE-SW and dipping 70°/SE. The main ore minerals are represented by gold, chalcopyrite, pyrite, sphalerite, malachite, covellite and goethite. While, geffroyite, cuprite, chrysocolla, pseudomalachite, britholite, wolframite, scheelite, hematite and rutile are detected as minor constituents. Fluid inclusions microthermometry and isochore calculations combined with chlorite geothermometry revealed that the Um Balad deposits were formed at temperature ranging from 305 °C to 325 °C and pressure between (100-500 bar). The mineralization had been developed in the shallow levels, beneath the water table at depth of 350-1760 m, rather than common mesothermal vein-type deposits in Egypt. Magmatic water have been suggested as the main source for the mineralized fluid. The transportation of the gold metal seems to be happen as bisulfide complexes in moderately acidic environment. The deposition was resulted from combination of changes in physico-chemical parameters, temperature and pressure plus the instability of the reduced sulfur complexes. A contamination with metamorphic and/or meteoric water was also proposed that has strong influence during the depositional process.

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

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

Moran, James J.; Whitmore, Laura M.; Jay, Zackary J.

Volcanism and post-magmatism contribute significant annual methane (CH 4) fluxes to the atmosphere (on par with other natural sources such as forest fire and wild animal emissions) and have been implicated in past climate-change events. The Yellowstone hot spot is one of the largest volcanic systems on Earth and is known to emit CH 4 (as well as carbon dioxide (CO 2) and other gases), but the ultimate sources of this CH 4 flux have not been elucidated. In this paper, we use dual stable isotope analysis (δ 2H and δ 13C) of CH 4 sampled from ten high-temperature geothermalmore » pools in Yellowstone National Park along with other isotopic and gas analyses to evaluate potential sources of methane. The average δ 13C and δ 2H values of CH 4 emitted from hot springs ( 26.7 (± 2.4) and - 236.9 (± 12.0) ‰, respectively) are inconsistent with microbial methanogenesis but do not allow distinction between thermogenic and abiotic sources. Correlation between δ 13C CH4 and δ 13C of dissolved inorganic C (DIC) is consistent with DIC as the parent C source for the observed CH 4, or with equilibration of CH 4 and DIC. Methane formation temperatures estimated by isotopic geothermometry based on δ 13C CH4 and δ 13C CO2 ranged from ~ 250–350 °C, which is just below previous temperature estimates for the hydrothermal reservoir. Further, the δ 2H H2O of the thermal springs and the measured δ 2H CH4 values are consistent with equilibration between the source water and the CH 4 at the formation temperatures. Though the ultimate origin of the CH 4 could be attributed to either abiotic of themorgenic processes with subsequent isotopic equilibration, the C 1/C 2+ composition of the gases is more consistent with abiotic origins for most of the samples. Finally, our data support the hypothesis that subsurface rock-water interactions are responsible for at least a significant fraction of the CH 4 flux from the Yellowstone National Park volcanic system.« less

The Influence of Grain Boundary Fluids on the Recrystallization Behavior in Calcite: A Comparison of "dry" and "wet" Marble Mylonites

NASA Astrophysics Data System (ADS)

Schenk, O.; Urai, J.; Evans, B.

2003-12-01

Carbonate rocks are able to accumulate large amounts of strain and deform crystal-plastically even at low p-T conditions and thus, marble sequences are often the site of strain localization in the upper crust during late-stage deformation in mountain building processes. In this study we sought to identify the effect of fluids on grain boundary morphology and recrystallization processes in marble mylonites during shear zone evolution, as fluids play a major role in the flow behavior of many rock materials during deformation (e.g. quartz, olivine, halite, feldspar). We compared calcite marble mylonites from two geological settings: (a) Schneeberg Complex, Southern Tyrole, Italy and (b) Naxos Metamorphic Core Complex, Greece. The shear zones of the selected areas are suitable for comparison, because they consist of similar lithology and the marble mylonites resemble each other in chemical composition. In addition, calcite-dolomite solvus geothermometry and TEM observations indicate similar p-T conditions for the shear zones formation. However, the two settings are different in the availability of fluids during the shear zone evolution: In the Schneeberg mylonites, both the alteration of minerals during retrograde metamorphism of neighboring micaschists and the existence of veins suggest that fluids were present during mylonitization. The absence of these features in the Naxos samples indicates that fluids were not present during deformation of these mylonites. This difference is also supported by the signature of stable isotopes. Microstructural investigations using optical and scanning electron microscopes on broken and planar surfaces did not indicate major differences between wet and dry mylonites: Grain boundaries of both types of samples display pores with shapes controlled by crystallography, and pore morphologies that are similar to observations from crack and grain-boundary healing experiments. Grain size reduction was predominantly the result of subgrain rotation recrystallization. However, the coarse grains inside the wet protomylonites (Schneeberg) are characterized by intracrystalline shear zones. With the exception of the intracrystalline shear zones, there were no obvious microstructural signatures that were obvious indicators of the presence of fluids, at least for these two field examples.

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

DOE PAGES

Moran, James J.; Whitmore, Laura M.; Jay, Zackary J.; ...

2017-05-16

Volcanism and post-magmatism contribute significant annual methane (CH 4) fluxes to the atmosphere (on par with other natural sources such as forest fire and wild animal emissions) and have been implicated in past climate-change events. The Yellowstone hot spot is one of the largest volcanic systems on Earth and is known to emit CH 4 (as well as carbon dioxide (CO 2) and other gases), but the ultimate sources of this CH 4 flux have not been elucidated. In this paper, we use dual stable isotope analysis (δ 2H and δ 13C) of CH 4 sampled from ten high-temperature geothermalmore » pools in Yellowstone National Park along with other isotopic and gas analyses to evaluate potential sources of methane. The average δ 13C and δ 2H values of CH 4 emitted from hot springs ( 26.7 (± 2.4) and - 236.9 (± 12.0) ‰, respectively) are inconsistent with microbial methanogenesis but do not allow distinction between thermogenic and abiotic sources. Correlation between δ 13C CH4 and δ 13C of dissolved inorganic C (DIC) is consistent with DIC as the parent C source for the observed CH 4, or with equilibration of CH 4 and DIC. Methane formation temperatures estimated by isotopic geothermometry based on δ 13C CH4 and δ 13C CO2 ranged from ~ 250–350 °C, which is just below previous temperature estimates for the hydrothermal reservoir. Further, the δ 2H H2O of the thermal springs and the measured δ 2H CH4 values are consistent with equilibration between the source water and the CH 4 at the formation temperatures. Though the ultimate origin of the CH 4 could be attributed to either abiotic of themorgenic processes with subsequent isotopic equilibration, the C 1/C 2+ composition of the gases is more consistent with abiotic origins for most of the samples. Finally, our data support the hypothesis that subsurface rock-water interactions are responsible for at least a significant fraction of the CH 4 flux from the Yellowstone National Park volcanic system.« less

Constraining the thermal structure beneath Lusi: insights from temperature record in erupted clasts

NASA Astrophysics Data System (ADS)

Malvoisin, Benjamin; Mazzini, Adriano; Miller, Stephen

2016-04-01

Sedimentary units beneath Lusi from surface to depth are the Pucangan formation, the Upper Kalibeng formation where shales and then volcanoclastic clasts are found, the Kujung-Propuh-Tuban formation composed of carbonates and the Ngimbang formation composed of shales. Water and gas geochemistry as well as surface deformation indicate that Lusi is a hydrothermal system rooted at >4 km depth. However, the thermal structure beneath Lusi is still poorly constrained whereas it has first-order impacts on the physical and chemical processes observed during the eruption. In the framework of the Lusi Lab project (ERC grant n° 308126) and of a project of the Swiss National Science Foundation (n°160050) we studied erupted clasts collected at the crater site to determine their source and temperature record. Three types of clasts were studied based on morphological and mineralogical basis. The first type is limestones mainly composed of Ca- and Fe-bearing carbonates. The clasts of the second type are light grey shales (LGS) containing carbonaceous matter, illite/smectite mixture, plagioclase and quartz. The third type is also a shale with a black colour containing hydrocarbons (black shales, BS) and with the additional presence of Na-rich plagioclase, biotite and chlorite. The presence of these latter minerals indicates hydrothermal activity at relatively high temperature. Better constraints on temperature were obtained by using both Raman spectroscopic carbonaceous material thermometry (RSCM) and chlorite geothermometry. Temperatures below 200°C were determined for the LGS with RSCM. BS recorded two temperatures. The first one, around 170°C, is rather consistent with an extrapolation of the geothermal gradient measured before the eruption up to 4,000 m depth. Combined with mineralogical observations, this suggests that BS originate from the Ngimbang formation. The second recorded higher temperature around 250°C indicates heating, probably through interaction with high temperature hydrothermal fluids. Calculations performed for such a heating indicate that associated clay dehydration is sufficient to provide the water released during the eruption and that heating-induced overpressure could favor fluid ascent. These results confirm the hydrothermal scenario in which Lusi eruption is fed by high temperature fluid circulation from the neighboring Arjuno-Welirang volcanic complex.

Dual stable isotopes of CH4 from Yellowstone hot-springs suggest hydrothermal processes involving magmatic CO2

NASA Astrophysics Data System (ADS)

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

2017-07-01

Volcanism and post-magmatism contribute significant annual methane (CH4) fluxes to the atmosphere (on par with other natural sources such as forest fire and wild animal emissions) and have been implicated in past climate-change events. The Yellowstone hot spot is one of the largest volcanic systems on Earth and is known to emit CH4 (as well as carbon dioxide (CO2) and other gases), but the ultimate sources of this CH4 flux have not been elucidated. Here we use dual stable isotope analysis (δ2H and δ13C) of CH4 sampled from ten high-temperature geothermal pools in Yellowstone National Park along with other isotopic and gas analyses to evaluate potential sources of methane. The average δ13C and δ2H values of CH4 emitted from hot springs (26.7 (± 2.4) and - 236.9 (± 12.0) ‰, respectively) are inconsistent with microbial methanogenesis but do not allow distinction between thermogenic and abiotic sources. Correlation between δ13CCH4 and δ13C of dissolved inorganic C (DIC) is consistent with DIC as the parent C source for the observed CH4, or with equilibration of CH4 and DIC. Methane formation temperatures estimated by isotopic geothermometry based on δ13CCH4 and δ13CCO2 ranged from 250-350 °C, which is just below previous temperature estimates for the hydrothermal reservoir. Further, the δ2HH2O of the thermal springs and the measured δ2HCH4 values are consistent with equilibration between the source water and the CH4 at the formation temperatures. Though the ultimate origin of the CH4 could be attributed to either abiotic of themorgenic processes with subsequent isotopic equilibration, the C1/C2 + composition of the gases is more consistent with abiotic origins for most of the samples. Thus, our data support the hypothesis that subsurface rock-water interactions are responsible for at least a significant fraction of the CH4 flux from the Yellowstone National Park volcanic system.

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

NASA Astrophysics Data System (ADS)

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

2015-12-01

Subsurface fluid flow is strongly influenced by faults and fractures, yet the transmissivity of faults and fractures changes through time due to deformation and cement precipitation, making flow paths difficult to predict. Here we assess past fracture connectivity in an active hydrothermal system in the Basin and Range, Nevada, USA, using clumped isotope geochemistry and cold cathodoluminescence (CL) analysis of fracture filling cements from the Blue Mountain geothermal field. Calcite cements were sampled from drill cuttings and two cores at varying distances from faults. CL microscopy of some of the cements shows banding parallel to the fracture walls as well as brecciation, indicating that the cements record variations in the composition and source of fluids that moved through the fractures as they opened episodically. CL microscopy, δ13C and δ18O values were used to screen homogeneous samples for clumped isotope analysis. Clumped isotope thermometry of most samples indicates paleofluid temperatures of around 150°C, with several wells peaking at above 200°C. We suggest that the consistency of these temperatures is related to upwelling of fluids in the convective hydrothermal system, and interpret the similarity of the clumped isotope temperatures to modern geothermal fluid temperatures of ~160-180°C as evidence that average reservoir temperatures have changed little since precipitation of the calcite cements. In contrast, two samples, one of which was associated with fault gauge observed in drill logs, record significantly cooler temperatures of 19 and 73°C and anomalous δ13C and δ18Owater values, which point to fault-controlled pathways for downwelling meteoric fluid. Finally, we interpret correspondence of paleofluid temperatures and δ18Owater values constrained by clumped isotope thermometry of calcite from different wells to suggest past connectivity of fractures among wells within the geothermal field. Results show the ability of clumped isotope geothermometry to assess fracture connectivity and geothermal reservoir characteristics in the past—with the potential to help optimize resource production and injection programs and better understand structural controls on mass and heat transfer in the subsurface.

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.

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.

Basanite-nephelinite suite from early Kilauea: carbonated melts of phlogopite-garnet peridotite at Hawaii's leading magmatic edge

NASA Astrophysics Data System (ADS)

Sisson, T. W.; Kimura, J.-I.; Coombs, M. L.

2009-12-01

A basanite-nephelinite glass suite from early submarine Kilauea defines a continuous compositional array marked by increasing concentrations of incompatible components with decreasing SiO2, MgO, and Al2O3. Like peripheral and post-shield strongly alkalic Hawaiian localities (Clague et al. in J Volcanol Geotherm Res 151:279-307, 2006; Dixon et al. in J Pet 38:911-939, 1997), the early Kilauea basanite-nephelinite glasses are interpreted as olivine fractionation products from primary magnesian alkalic liquids. For early Kilauea, these were saturated with a garnet-phlogopite-sulfide peridotite assemblage, with elevated dissolved CO2 contents responsible for the liquids’ distinctly low-SiO2 concentrations. Reconstructed primitive liquids for early Kilauea and other Hawaiian strongly alkalic localities are similar to experimental 3 GPa low-degree melts of moderately carbonated garnet lherzolite, and estimated parent magma temperatures of 1,350-1,400°C (olivine-liquid geothermometry) match the ambient upper mantle geotherm shortly beneath the base of the lithosphere. The ~3 GPa source regions were too hot for stable crystalline carbonate and may have consisted of ambient upper mantle peridotite containing interstitial carbonate-silicate or carbonatitic liquid, possibly (Dixon et al. in Geochem Geophys Geosyst 9(9):Q09005, 2008), although not necessarily, from the Hawaiian mantle plume. Carbonate-enriched domains were particularly susceptible to further melting upon modest decompression during upward lithospheric flexure beneath the advancing Hawaiian Arch, or by conductive heating or upward drag by the Hawaiian mantle plume. The early Kilauea basanite-nephelinite suite has a HIMU-influenced isotopic character unlike other Hawaiian magmas (Shimizu et al. in EOS Tran Amer Geophys Union 82(47): abstr V12B-0962, 2001; Shimizu et al. in Geochim Cosmochim Acta 66(15A):710, 2002) but consistent with oceanic carbonatite involvement (Hoernle et al. in Contrib Mineral Petrol 142:520-542, 2002). It may represent the melting products of a fertile domain in the ambient upper mantle impinged upon and perturbed by the sustained plume source that feeds later shield-stage magmatism.

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

NASA Astrophysics Data System (ADS)

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

2004-12-01

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

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.

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.

Isotopic and geothermometric constraints on the structural and metamorphic evolution of Homestake gold deposit, Black Hills, South Dakota (USA)

NASA Astrophysics Data System (ADS)

Terry, M.; Dahl, P.; Frei, R.

2003-04-01

The Homestake Deposit, located in the northern Black Hills and host for 40 million ounces of gold, shows evidence for extensive remobilization of gold related to regional metamorphism deformation associated with the Early Proterozoic assembly of supercontinent Laurentia. Field and petrographic evidence for gold remobilization includes the occurrence of abundant quartz veins associated with selvages of chlorite-siderite-ankerite-pyrrhotite-arsenopyrite-gold in the Homestake Fm. The deposit is located on the western limb of a major anticlinorium that coincides with a vertical N-S-striking garnet isograd, and garnet-biotite geothermometry of metapelites sampled across the anticlinorium indicates a steep metamorphic field gradient of 150^oC/km (east side warmer). This gradient is mirrored by a pronounced fractionation of oxygen isotopes observed in the vein quartz, with δ18O ranging from 10 to 18 ppm. The isograd is parallel with a major N-S-striking shear zone, and kinematic indicators predominantly indicate oblique sinistral motion with east-side up. Garnet was separated from a subsurface sample of the Homestake Fm. collected from the nose of the so-called "main ledge" synform and subjected to Pb stepwise leaching (PbSL) to determine the age of garnet growth and thus metamorphism. PbSL analysis revealed a 207Pb/206Pb age of 1746 ± 10 Ma (± 2σ). Recent work in the southern Black Hills indicates that almandine does not contain sufficient Pb to be dated directly by this method; instead, the PbSL result represents the bulk age of abundant allanite inclusions observed in the garnet. Thus, 1746 Ma is interpreted as a maximum age of prograde garnet growth during regional thermotectonism. Mineral assemblages from selvages in Main Ledge indicate that mineralization occurred at or after peak metamorph, which indicates that 1746 Ma also represents a maximum age for gold remobilization. A minimum 1715 Ma age of these events is indicated by published ages of post-tectonic leucogranite in the Black Hills. Regionally, the N-S orientation, 1746--1715 Ma timing, and sinistral-transpressive motion combine to suggest that this major shear zone in the northern Black Hills represents a northerly extension of the Hartville fault, which is exposed in SE Wyoming, ˜200 km SSW. Correlation of these shear zones would have important implications for Proterozoic terrane assembly in this part of Laurentia.

Patchy distribution of magma that fed the Bishop Tuff supereruption: Evidence from matrix glass major and trace-element compositions

NASA Astrophysics Data System (ADS)

Gualda, G. A. R.; Ghiorso, M. S.; Hurst, A. A.; Allen, M. C.; Bradshaw, R. W.

2017-12-01

For more than 40 years, the Bishop Tuff has been the archetypical example of a singular, zoned magma body that fed a supereruption. Early-erupted material is pyroxene-free and crystal poor (<20 wt. %), presumably erupted from the upper parts of the magma body; late-erupted material is orthopyroxene and clinopyroxene-bearing, commonly more crystal rich (up to 30 wt. % crystals), and presumably tapped magma from the lower portions of the magma body. Fe-Ti oxide compositions suggest higher crystallization temperatures for late-erupted magmas (as high as 820 °C) than for early-erupted magmas (as low as 700 °C). Pressures and temperatures derived from major element compositions of glass inclusions led Gualda & Ghiorso (2013, CMP) to suggest an alternative model of lateral juxtaposition of two main magma bodies - each one feeding early-erupted and late-erupted units. Chamberlain et al. (2015, JPet) and Evans et al. (2016, AmMin) recently disputed this interpretation. We present a large dataset of matrix glass compositions for 161 pumice clasts that span the stratigraphy of the deposit. We calculate crystallization pressures based on major-element glass compositions using rhyolite-MELTS geobarometry, and crystallization temperatures based on Zr in glass using zircon saturation geothermometry. We apply the same methods to 1538 major-element and 615 trace-element analyses from Chamberlain et al. The results overwhelmingly demonstrate that there is no difference in crystallization temperature or pressure between early and late-erupted magmas. Crystallization pressures and temperatures are unimodal, with modes of 150 MPa and 730 °C (calibration of Watson & Harrison). Our results strongly support lateral juxtaposition of two main magma bodies. Smaller units recognized by Chamberlain et al. crystallized at the same pressures as the main bodies - this suggests the coexistence of larger and smaller magma bodies at the time of the Bishop Tuff supereruption. We compare our findings for the Bishop Tuff with results for very large and supereruptions elsewhere in the world. We argue that supereruptions typically mobilize a complex patchwork of magma bodies that reside within specific levels of the crust. They reveal moments of high-melt productivity in the crust, unlike what we observe in the Earth today.

Geochemical and textural characterization of phosphate accessory phases in the vein assemblage and metasomatically altered Llallagua tin porphyry

NASA Astrophysics Data System (ADS)

Betkowski, Wladyslaw B.; Rakovan, John; Harlov, Daniel E.

2017-09-01

Petrographic and geochemical characterization of phosphate accessory minerals represents a powerful tool in understanding the mineralization and metasomatic history of one of the world's biggest tin deposits, the Siglo XX mine, Salvadora stock, Llallagua, Bolivia. The Llallagua tin deposit lies in a hydrothermally altered porphyry stock that is part of the subduction-related Bolivian tin belt. Despite numerous studies, there is still a debate over the timing and characteristics of mineralization history of the deposit. Primary igneous fluorapatite and monazite (for the first time) were recognized in the altered porphyry. The igneous monazite is enriched in Th, unlike the hydrothermal monazite that is recognized for its low Th concentration. Fluorapatite, monazite, and xenotime also coexist with cassiterite within the hydrothermal vein assemblage. Fluorapatite and xenotime are essentially pristine. Monazite, however, shows various degrees of alteration in the form of regenerative mineral replacement (RMR). This exemplifies differential reactivity and selective mineral replacement/alteration of three accessory phosphate minerals, that are all important geochemical tracers of magmatic and hydrothermal processes, and which can all be used as geochronometers. Mineral textures and composition in the altered porphyry and vein assemblages have been evaluated. Monazite-xenotime geothermometry indicates monazite crystallization beginning around 550 °C. Monazite continues to grow as temperatures gradually decrease to about 300 °C, when most of cassiterite precipitation occurred in the samples studied. The primary mechanism of phosphate alteration has been identified as a coupled dissolution-reprecipitation process, which led to REE exchange in the igneous fluorapatite and hydrothermal monazite. In Type I local alteration, La and Pr-Nd show continuity across the pre- and post- alteration concentric zones indicating that they were not affected by alteration. This is an example of a selective elemental exchange during coupled dissolution-precipitation. Type II, pervasive post-growth alteration, is evident by the presence of micro-porosity and the formation of secondary, reaction induced minerals. Release of HREE from the monazite goes into the formation of void filling xenotime inclusions; the first documentation of this metasomatic alteration product in monazite. A well-documented discrepancy exists among ages determined from the zircon, fluorapatite, monazite, and altered porphyry minerals. These observations, regarding selective alteration of fluorapatite and monazite, may help to elucidate the reasons for this discrepancy.

The length of channelized lava flows: Insight from the 1859 eruption of Mauna Loa Volcano, Hawai‘i

NASA Astrophysics Data System (ADS)

Riker, Jenny M.; Cashman, Katharine V.; Kauahikaua, James P.; Montierth, Charlene M.

2009-06-01

The 1859 eruption of Mauna Loa Volcano, Hawai'i, produced paired 'a'ā and pāhoehoe flows of exceptional length (51 km). The 'a'ā flow field is distinguished by a long (> 36 km) and well-defined pāhoehoe-lined channel, indicating that channelized lava remained fluid to great distances from the vent. The 1859 eruption was further unusual in initiating at a radial vent on the volcano's northwest flank, instead of along the well-defined rift zone that has been the source of most historic activity. As such, it presents an opportunity both to examine controls on the emplacement of long lava channels and to assess hazards posed by future flank eruptions of Mauna Loa. Here we combine evidence from historical chronicles with analysis of bulk compositions, glass geothermometry, and microlite textures of samples collected along the 1859 lava flows to constrain eruption and flow emplacement conditions. The bulk compositions of samples from the 'a'ā and pāhoehoe flow fields are bimodally distributed and indicate tapping of two discrete magma bodies during eruption. Samples from the pāhoehoe flow field have bulk compositions similar to those of historically-erupted lavas (< 8 wt.% MgO); lava that fed the 'a'ā channel is more primitive (> 8 wt.% MgO), nearly aphyric, and was erupted at high temperatures (1194-1216 °C). We suggest that the physical properties of proximal channel-fed lava (i.e., high-temperature, low crystallinity, and low bulk viscosity) promoted both rapid flow advance and development of long pāhoehoe-lined channels. Critical for the latter was the large temperature decrease (~ 50 °C) required to reach the point at which plagioclase and pyroxene started to crystallize; the importance of phase constraints are emphasized by our difficulty in replicating patterns of cooling and crystallization recorded by high-temperature field samples using common models of flow emplacement. Placement of the 1859 eruption within the context of historic activity at Mauna Loa suggests that the formation of radial vents and eruptions of high-temperature magma may not only be linked, but may also be a consequence of periods of high magma supply (e.g., 1843-1877). Flank eruptions could therefore warrant special consideration in models and hazard mitigation efforts.

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

NASA Astrophysics Data System (ADS)

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

2013-03-01

Sulphur Springs is a vigorous, geothermal field associated with the active Soufrière Volcanic Centre in southern Saint Lucia, Lesser Antilles island arc. The 'Sulphur Springs Park' is an important tourist attraction (touted as the 'world's only drive-through volcano') with some of the hot pools being developed into recreational pools. Some 200,000 people visit the park each year. Since 2001, the hydrothermal fluids of Sulphur Springs have been sampled as part of an integrated volcanic monitoring programme for the island. Gas and water samples were analysed to characterise the geochemistry of the hydrothermal system, and to assess the equilibrium state and subsurface temperatures of the reservoir. This has also enabled us, for the first time, to establish baseline data for future geochemical monitoring. The gases are of typical arc-type composition, with N2 excess and low He and Ar content. The dry gas composition is dominated by CO2 (ranging from 601-993 mmol/mol), with deeper magmatic sourced H2S-rich vapour undergoing boiling and redox changes in the geothermal reservoir to emerge with a hydrothermal signature in the fumarolic gases. Fluid contributions from magmatic degassing are also evident, mainly from the moderate to high contents of HCl and deeply-sourced H2S gas, respectively. Sulphur Springs hydrothermal waters have acid-sulphate type compositions (SO4 = 78-4008 mg/L; pH = 3-7), and are of primarily meteoric origin which have been affected by evaporation processes based on the enrichment in both δ18O and δD (δ18O = - 1 to 15‰ and δD = - 9 to 14‰ respectively) in relation to the global meteoric water line (GMWL). These waters are steam-heated water typically formed by absorption of H2S-rich gases in the near surface oxygenated groundwaters. Reservoir temperatures calculated from the evaluation of gas equilibria in the CO2-CH4-H2 system reveal higher temperatures (190 to 300 °C) than those derived from quartz geothermometry (95 to 169 °C), which appeared to be affected by dilution with meteoric waters. Generally, no significant variations in fluid geochemistry of the hydrothermal system were observed between 2001 and 2006, and we propose that there were no changes in the state of volcanic activity during this period.

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

NASA Astrophysics Data System (ADS)

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

2018-04-01

The aim of this experimental study was to investigate the incorporation of Na in cordierite in metapelites as a function of temperature and pressure using natural quartzphyllite rocks as starting materials. The experiments were performed in a hydrothermal apparatus as well as a piston-cylinder apparatus with two natural quartzphyllite samples, which represent the protolith rocks of the hornfelses from the Brixen Granite contact aureole near Franzensfeste. Sample W shows high muscovite contents (57 wt%) and only accessory plagioclase while sample SP5 has high plagioclase (16 wt%) and lower muscovite contents (20 vol%). The experiments were done dry at pressures of 0.15, 0.3 and 0.6 GPa in a temperature range of 550 °C to 780 °C. The Na content of the newly formed cordierites shows a systematic variation and decreases linearly with increasing temperatures and no influence of pressure and melting on the Na contents of cordierite was observed. The experiments also show that the difference in mineral assemblage considerably shifts the obtained Na contents of cordierite. The P-independent temperature correlations for both sets of experiments can be described with the linear relationships: T (°C) = (Na [apfu] - 0.4052)/(-0.000487); R2 = 0.96; (±20 °C, calibration W) and T (°C) = (Na [apfu] - 0.3671)/(-0.000383); R2 = 0.94; (±15 °C, calibration SP5). The difference between the two temperatures is large and the SP5 experiments yield temperatures that are up to 100 °C higher. This is not unexpected since theoretical phase relations in the system NMASH predict different Na contents depending on the buffering assemblage (plagioclase vs. paragonite). On the other hand these T differences could also reflect disequilibrium behaviour in the SP5 experiments. Detailed micro-Raman spectroscopic investigations reveal that cordierites from both experiments show disordered structures but the SP5 experiments show a much higher degree of Si-Al disorder and the elevated Na contents could reflect this disequilibrium behaviour. Preliminary geothermometric calculations using the data from the W experiments are in very good agreement with T estimates from conventional geothermometry in metapelitic contact aureoles as well as high-grade migmatic gneisses from the literature.

Mineral chemistry of Pangidi basalt flows from Andhra Pradesh

NASA Astrophysics Data System (ADS)

Nageswara Rao, P. V.; Swaroop, P. C.; Karimulla, Syed

2012-04-01

This paper elucidates the compositional studies on clinopyroxene, plagioclase, titaniferous magnetite and ilmenite of basalts of Pangidi area to understand the geothermometry and oxybarometry conditions. Petrographic evidence and anorthite content (up to 85%) of plagioclase and temperature estimates of clinopyroxene indicate that the clinopyroxene is crystallized later than or together with plagioclase. The higher An content indicates that the parent magma is tholeiitic composition. The equilibration temperatures of clinopyroxene (1110-1190°C) and titaniferous magnetite and ilmenite coexisting mineral phases (1063-1103°C) are almost similar in lower basalt flow and it is higher for clinopyroxene (900-1110°C) when compared to titaniferous magnetite and ilmenite coexisting mineral phases (748-898°C) in middle and upper basalt flows. From this it can be inferred that the clinopyroxene is crystallized earlier than Fe-Ti oxide phases reequilibration, which indicates that the clinopyroxene temperature is the approximate eruption temperature of the present lava flows. The wide range of temperatures (900-1190°C) attained by clinopyroxene may point out that the equilibration of clinopyroxene crystals initiated from depth till closer to the surface before the melt erupted. Pangidi basalts follow the QFM buffer curve which indicates the more evolved tholeiitic composition. This suggests the parent tholeiitic magma suffered limited fractionation at high temperature under increasing oxygen fugacity in lower basalt flow and more fractionation at medium to lower temperatures under decreasing oxygen fugacity conditions during cooling of middle and upper basalt flows. The variation of oxygen fugacity indicates the oxidizing conditions for lower basalt flow (9.48-10.3) and extremely reducing conditions for middle (12.1-15.5) and upper basalt (12.4-15.54) flows prevailed at the time of cooling. Temperature vs. (FeO+Fe2O3)/(FeO+Fe2O3 +MgO) data plots for present basalts suggested the lower basaltic flow is formed at higher temperatures while the middle and upper basalt flows at medium to lower temperatures. The lower basalt flow is represented by higher temperatures which shows high modal values of opaques and glass whereas the medium to lower temperatures of middle and upper flow are caused by vesicular nature which contain larger content of gases and humid to semi-arid conditions during cooling.

Comparison of Geothermobarometers with Different Closure Behavior to Constrain P-T Paths

NASA Astrophysics Data System (ADS)

Hora, J.; Simon, K.; Kronz, A.; Xiao, Y.; Worner, G.

2014-12-01

Temperatures obtained from geothermobarometers depend not only on minerals reaching equilibrium, but also on preservation of those compositions through subsequent thermal history. In the case of step-function cooling histories (volcanic systems), each of several geothermometry equations (with P-dependence) can be treated as a line in P-T space for a given composition. In the absence of independent P-constraint, intersection of those lines corresponds to the simultaneous solution of the equations involved and is indicative of crystallization and storage conditions. Multiple calibrations of a given thermometer can be evaluated by their degree of match. For protracted plutonic or metamorphic cooling histories, a single intersection is not expected - instead, calculated temperatures will reflect a sequence of mineral closure based on diffusivity of the element(s) of interest in the various phases. We apply this multi-thermometer approach to quartz, rutile, and titanite formed along the retrograde path in gneiss and eclogite at Bixiling, Dabie UHP terrane, China. Using the Huang and Audetat (2012) Ti-in-quartz thermometer calibration, all available Zr-in-rutile equations intersect at approximately 7-10 kbar and 560-580°C. Zr-in-rutile calibrations diverge at higher P, and intersect the Thomas et al. (2010) Ti-in-quartz calibration over a broader range of 13-16 kbar and 550-600°C. Regardless of which intersection is used, it appears that both of these minerals have reequilibrated far below the previously reported peak conditions of >30 kbar and >750°C. Titanite, where diffusion is slower, is present in the gneiss unit as late-stage overgrowths on rutile, but records T that are approximately 150°C higher than the rutile inclusions at all P. This appears to be consistent with all minerals forming above 750°C and possibly much higher P, with quartz and rutile being reset along the retrograde path due to more rapid diffusion. When crystal sizes are taken into account, rutile and quartz are predicted to close to Zr and Ti exchange at similar T ≈ 600-650°C. Intersections of P-T lines among two or more minerals with similar closure behavior may reflect P,T at points along a retrograde path or can be used to constrain cooling rate, and may have advantages relative to using a single thermobarometer.

How to Simulate the Interplate Domain in Thermo-mechanical Experiments of Subduction ? Critical Effects of Resolution and Rheology, and Consequences on Wet Mantle Melting

NASA Astrophysics Data System (ADS)

Arcay, D.

2017-12-01

Oceanic plate subduction implies tight interactions between converging lithospheres and surrounding mantle. Plate-mantle couplings can be modeled using thermo-chemical codes of mantle convection. But how to model correctly with a continuous fluid approach the subduction interface, characterised by strong and localised discontinuities? The present study aims at better deciphering the different mechanisms involved in the functioning of the subduction interplate, simply modeled by a weak crust layer, free to evolve. Pseudo-brittle and non-Newtonian behaviours are modelled. This study shows first that the numerical resolution is critical. If the subducting plate is 100 Myr old, subduction occurs for any crust strength. The stiffer the crust is, the shallower the interplate down-dip extent is and the hotter the fore-arc base is. Conversely, imposing a very weak subduction channel leads to an extreme mantle wedge cooling and inhibits mantle melting in wet conditions. If the incoming plate is 20 Myr old, subduction occurs only if the crust is either stiff and denser than the mantle, or weak and buoyant. These conditions lead notably to (1) fore-arc lithosphere cooling, and (2) partial or complete hindrance of wet mantle melting. Finally, subduction plane dynamics is intimately linked to the regime of subduction-induced corner flow: either focussed towards the mantle wedge tip and strongly warming the subduction plate, or, diffuse and favoring global cooling by the lengthening of the subduction plane. The thermal states simulated within the mantle wedge are compared with observations to decipher the best rheological ranges modelling the subduction channel. Two intervals of crustal activation energy are underlined: 345-385 kJ/mol to reproduce the slab surface temperature range inferred from geothermometry, and 415-455 kJ/mol to reproduce the hot mantle wedge core suggested by seismic tomographies. As these two intervals do not overlap, an extra process involved in subduction dynamics is needed. A moderate mantle viscosity reduction, caused by metasomatism in the mantle wedge, is proposed. From these results, it can be inferred that the subduction channel down-dip extent should vary with the subduction setting, consistently with the worldwide variability of sub-arc depths of the subducting plate surface.

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.

Metal endowment reflected in chemical composition of silicates and sulfides of mineralized porphyry copper systems, Urumieh-Dokhtar magmatic arc, Iran

NASA Astrophysics Data System (ADS)

Zarasvandi, Alireza; Rezaei, Mohsen; Raith, Johann G.; Pourkaseb, Houshang; Asadi, Sina; Saed, Madineh; Lentz, David R.

2018-02-01

The present work attempts to discriminate between the geochemical features of magmatic-hydrothermal systems involved in the early stages of mineralization in high grade versus low grade porphyry copper systems, using chemical compositions of silicate and sulfide minerals (i.e., plagioclase, biotite, pyrite and chalcopyrite). The data indicate that magmatic plagioclase in all of the porphyry copper systems studied here has high An% and Al content with a significant trend of evolution toward AlAl3SiO8 and □Si4O8 endmembers, providing insight into the high melt water contents of the parental magmas. Comparably, excess Al and An% in the high grade deposits appears to be higher than that of selected low grade deposits, representing a direct link between the amounts of exsolving hydrothermal fluids and the potential of metal endowment in porphyry copper deposits (PCDs). Also, higher Al contents accompanied by elevated An% are linked to the increasing intensity of disruptive alteration (phyllic) in feldspars from the high grade deposits. As calculated from biotite compositions, chloride contents are higher in the exsolving hydrothermal fluids that contributed to the early mineralization stages of highly mineralized porphyry systems. However, as evidenced by scattered and elevated log (fH2O)/(fHF) and log (fH2O)/(fHCl) values, chloride contents recorded in biotite could be influenced by post potassic fluids. Geothermometry of biotite associated with the onset of sulfide mineralization indicates that there is a trend of increasing temperature from high grade to low grade porphyry systems. Significantly, this is coupled with a sharp change in copper content of pyrite assemblages precipitated at the early stages of mineralization such that Cu decreased with increasing temperature. Based on EMPA and detailed WDS elemental mapping, trace elements do not exhibit complex compositional zoning or solid solution in the sulfide structure. Nevertheless, significant amounts of Cu and Au are contained in pyrite assemblages as micro- to nano-sized inclusions, especially in the high grade fertile porphyry deposits. However, unexpectedly high concentrations of Te, Se, and Re may be associated with early stage of sulfide mineralization, especially when there is no epithermal lithocap. This may highlight the significance of trace metals partitioning in the sulfides formed at the early stages of mineralization in PCDs.

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

NASA Astrophysics Data System (ADS)

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

2018-06-01

Gold-bearing sulfide-quartz veins cutting mainly through the Atalla monzogranite intrusion in the Eastern Desert of Egypt are controlled by subparallel NE-trending brittle shear zones. These veins are associated with pervasive sericite-altered, silicified, and ferruginated rocks. The hosting shear zones are presumed as high-order structures of the Najd-style faults in the Central Eastern Desert ( 615-585 Ma). Ore minerals include an early pyrite-arsenopyrite (±pyrrhotite) mineralization, partly replaced by a late pyrite-galena-sphalerite-chalcopyrite (±gold/electrum ± tetrahedrite ± hessite) assemblage. Gold occurs as small inclusions in pyrite and arsenopyrite, or more commonly as intergrowths with galena and sphalerite/tetrahedrite in microfractures. Arsenopyrite geothermometry suggests formation of the early Fe-As-sulfide mineralization at 380-340 °C, while conditions of deposition of the late base metal-gold assemblage are assumed to be below 300 °C. Rare hessite, electrum, and Bi-galena are associated with sphalerite and gold in the late assemblage. The early and late sulfide minerals show consistently a narrow range of δ34S ‰ (3.4-6.5) that overlaps with sulfur isotopic values in ophiolitic rocks. The Au-quartz veins are characterized by abundant CO2 and H2O ± CO2 ± NaCl inclusions, where three-dimensional clusters of inclusions show variable aqueous/carbonic proportions and broad range of total (bimodal) homogenization temperatures. Heterogeneous entrapment of immiscible fluids is interpreted to be caused by unmixing of an originally homogenous, low salinity ( 2 eq. mass % NaCl) aqueous-carbonic fluid, during transition from lithostatic to hydrostatic conditions. Gold deposition occurred generally under mesothermal conditions, i.e., 1.3 kbar and 280 °C, and continued during system cooling to < 200 °C and pressure decrease to 0.1 kbar. Based on the vein textures, sulfur isotope values, composition of ore fluids, and conditions of ore formation, we suggest that the Atalla monzogranite intrusion acted only as a competent structural host for ore deposition from shear-related, metal-rich fluids migrated up from depth. This model is also presumed for most granitoid-associated Au deposits in the region, considering the similarity in their structural control, alteration pattern and mineralogy, and chemistry of the ore fluids.

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

NASA Astrophysics Data System (ADS)

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

2017-12-01

The oscillation between explosive and effusive intermediate (59-62 wt% SiO2) volcanism in the Roseau Valley on Dominica, an island in the Lesser Antilles Arc, provides an opportunity to investigate temporal changes in the magmatic system. Here, we test the relationship between the Roseau ignimbrites (1-65 ka) and the Micotrin dome ( 1.1 ka) which are proposed to originate from the same magmatic system, with a detailed petrologic analysis of phenocrysts to determine commonalities or changes in pre-eruptive conditions (i.e., intensive variables). The ignimbrites are saturated in five phenocrysts (plagioclase + orthopyroxene + clinopyroxene + ilmenite + magnetite ± amphibole ± quartz), and the lava dome contains the same assemblage, but with notable differences: amphiboles are entirely reacted, and quartz occurs in greater abundance. Plagioclase in the ignimbrites ranges in composition from An46-93, and those in the dome range from An46-85. Two Fe-Ti oxide geo-thermometry reveal pre-eruptive temperatures from 730-820°C for three different ignimbrite units, whereas the pre-eruptive temperature for the dome is slightly hotter (850±23°C). Values of fO2 (relative to NNO) derived from Fe-Ti oxide oxygen-barometry range from +0.3 to +1.32 ΔNNO for the ignimbrites, which overlap with those from the dome (+0.5 to +0.9 ΔNNO). Pre-eruptive temperatures, plagioclase compositions, whole rock and glass compositions are incorporated into a plagioclase-liquid hygrometer to determine pre-eruptive melt H2O contents for each sample. H2O contents for ignimbrites range from 7.1-9.3 wt%, and those from the lava dome range from 6.7-7.1 wt%. Application of a H2O solubility model shows that water contents for the Roseau magmas correspond to pressures of 3-5 kbar. The most notable difference between the explosive and effusive magmas is that the lava dome has a higher pre-eruptive temperature than the ignimbrites. However, the results collectively suggest that more recent volcanism in the Roseau Valley (<5 ka) has hotter pre-eruptive temperatures, regardless of eruptive style, and that these intermediate magmas originate from sources in the deep crust (>5 kb). Understanding the magmatic system beneath Micotrin is important, as the capital of Roseau (pop. 15,000), is at the foot of the valley, built on old pyroclastic deposits.

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

NASA Astrophysics Data System (ADS)

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

2013-07-01

San Antonio Volcano, in the Tacaná Volcanic Complex, erupted ~ 1950 yr. B.P., with a Pelean type eruption that produced andesitic pyroclastic surges and block-and-ash flows destroying part of the volcano summit and producing a horse-shoe shaped crater open to the SW. Between 1950 and 800 yr B.P. the eruption continued with effusive andesites followed by a dacite lava flow and a summit dome, all from a single magma batch. All products consist of phenocrysts and microphenocrysts of zoned plagioclase, amphibole, pyroxene, magnetite ± ilmenite, set in partially crystallized groundmass of glass and microlites of the same mineral phases, except for the lack of amphibole. Included in the andesitic blocks of the block-and-ash flow deposit are basaltic andesite enclaves with elongated and ellipsoidal forms and chilled margins. The enclaves have intersertal textures with brown glass between microphenocrysts of plagioclase, hornblende, pyroxene, and olivine, and minor proportions of phenocrysts of plagioclase, hornblende, and pyroxene. A compositional range obtained of blocks and enclaves resulted from mixing between andesite (866 °C ± 22) and basaltic andesite (enclaves, 932 °C ± 22), which may have triggered the explosive Pelean eruption. Vestiges of that mixing are preserved as complex compositional zones in plagioclase and clinopyroxene-rich reaction rims in amphibole in the andesite. Whole-rock chemistry, geothermometry, experimental petrology and modeling results suggest that after the mixing event the eruption tapped hybrid andesitic magma (≤ 900 °C) and ended with effusive dacitic magma (~ 825 °C), all of which were stored at ~ 200 MPa water pressure. A complex open-system evolution that involved crustal end-members best explains the generation of effusive dacite from the hybrid andesite. Amphibole in the dacite is rimmed by reaction products of plagioclase, orthopyroxene, and Fe-Ti oxides produced by decompression during ascent. Amphibole in the andesite, however, lacks such rims. Because the andesite was at 866 ± 22 °C and the dacite was at ~ 825 °C, the reaction rims indicate that the andesitic magma ascended at 0.023 m s- 1 during the explosive phase of the eruption, whereas the dacitic magma rose more slowly at ~ 0.002-0.004 m s- 1.

Development of Genetic Occurrence Models for Geothermal Prospecting

NASA Astrophysics Data System (ADS)

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

2007-12-01

Exploration for utility-grade geothermal resources has mostly relied on identifying obvious surface manifestations of possible geothermal activity, e.g., locating and working near steaming ground or hot springs. This approach has lead to the development of over 130 resources worldwide, but geothermal exploration done in this manner is akin to locating hydrocarbon plays by searching for oil seeps. Confining exploration to areas with such features will clearly not discover a blind resource, that is, one that does not have surface expression. Blind resources, however, constitute the vast majority of hydrocarbon plays; this may be the case for geothermal resources as well. We propose a geothermal exploration strategy for finding blind systems that is based on an understanding of the geologic processes that transfer heat from the mantle to the upper crust and foster the conditions for hydrothermal circulation or enhanced geothermal exploration. The strategy employs a genetically based screening protocol to assess potential geothermal sites. The approach starts at the plate boundary scale and progressively focuses in on the scale of a producing electrical-grade field. Any active margin or hot spot is a potential location for geothermal resources. Although Quaternary igneous activity provides a clear indication of active advection of hot material into the upper crust, it is not sufficient to guarantee a potential utility-grade resource. Active faulting and/or evidence of high strain rates appear to be the critical features associated with areas of utility-grade geothermal potential. This is because deformation on its own can advect sufficient heat into the upper crust to create conditions favorable for geothermal exploitation. In addition, active deformation is required to demonstrate that open pathways for circulation of geothermal fluids are present and/or can be maintained. The last step in the screening protocol is to identify any evidence of geothermal activity, including high heat flow, anomalous temperature water wells, high-temperature indications from aqueous geothermometry and geochemistry, Pliocene or younger ages from low-temperature thermochronometers, as well as more obvious factors such as geysers and fumaroles (which by definition will be missing for blind resources). Our occurrence-model strategy inverts the current approach that relies first on obvious evidence of geothermal activity. We evaluated our approach by retrospectively applying the protocol to the characteristics of producing geothermal fields, and in all cases, known resource areas fit the parameters identified from a genetic perspective.

What do the Variscan structures in the Central Pyrenees tell us about the Mesozoic Iberian margin and the Pyrenean orogenic prism?

NASA Astrophysics Data System (ADS)

Lemirre, Baptiste; Cochelin, Bryan; de Saint Blanquat, Michel; Denele, Yoann; Lahfid, Abdeltif; Duchene, Stephanie

2017-04-01

The formation of the Pyrenean mountain belt since late Variscan times is responsible of the exhumation of the basement in the central part of the belt. This basement is mainly made of Proterozoic to Paleozoic rocks involved in the Variscan orogeny. Following the publication of the ECORS deep seismic profile of the Central Pyrenees in 1989, it has been proposed that the Pyrenees are an asymmetrical double verging belt implying crustal nappe stacking resulting from the inversion of the Iberian margin. Such alpine deformation implies important Meso-Cenozoic bloc rotations and internal deformation, overprinting the earlier Variscan deformations that would define the basement. In order to constrain how the crust was affected by both Variscan and Alpine orogenies, we present a structural and petrological study along the trace of the ECORS profile in the axial zone. The section is composed of Precambrian to Carboniferous low-grade metasedimentary rocks intruded by large late-Variscan calc-alkaline plutons. We highlight a transpressional event which can be divided into three progressive stages: (1) a N-S folding, producing regional-scale open to southward verging anticlines and synclines, prior to the metamorphic peak; (2) a strong N-S horizontal shortening synchronous to the maximum temperature recorded which increases from 500 °C in the north, to 350 °C in the south (Raman Spectroscopy of Carbonaceous Materials geothermometry combined with a petrological study). This deformation induces vertical stretching, isoclinal folding and formation of a steep pervasive cleavage defined by biotite and chlorite; (3) a strain localization into retrogressive reverse mylonitic shear zones, responsible for limited vertical offset of the sedimentary pile and a maximum offset of the isotherms of 50 °C. The presence of undeformed and unconformable Permian deposits at the top of the pile underlines the Variscan age of, at least, the two first stages of pervasive deformation. The continuity of Variscan structures, stratigraphy and isotherms all along the cross-section allows us to consider that the Axial Zone (the Iberian north margin) was only moderately affected by Cretaceous rifting, contrary to the European one. For the same reasons, we propose that the Axial Zone was neither affected by an intense pervasive deformation nor by large-scale internal rotation and vertical offset during the Alpine orogeny.

Preeruption conditions and timing of dacite-andesite magma mixing in the 2.2 ka eruption at Mount Rainier

NASA Astrophysics Data System (ADS)

Venezky, D. Y.; Rutherford, M. J.

1997-01-01

Analytical, field, and experimental evidence demonstrate that the Mount Rainier tephra layer C (2.2 ka) preserves a magma mixing event between an andesitic magma (whole rock SiO2 content of 57-60 wt %) and a dacitic magma (whole rock SiO2 content of 65±1 wt %). The end-member andesite (a mix of an injected and chamber andesite) and dacite can be characterized on the basis of the homogeneity of the matrix glass and phenocryst rim compositions. Many pumices, however, contain mixtures of the end-members. The end-member dacite contains a microlite-free matrix glass with 74-77 wt % SiO2, orthopyroxene rims of Mg57-64, clinopyroxene rims of Mg66-74, and plagioclase rim anorthite contents of An45-65. The temperature and oxygen fugacity, from Fe-Ti oxide compositions, are 930±10°C and 0.5-0.75 log units above NNO. The mixed andesite contains Mg73-84 orthopyroxene rims, Mg73-78 clinopyroxene rims, An78-84 plagioclase rims, and Mg67-74 amphibole rims. The temperature from Fe-Ti oxides, hornblendeplagioclase, and two-pyroxene geothermometry is 1060±15°C, and the oxygen fugacity is approximately one log unit above NNO for the injected andesite. The chamber andesite is estimated to be a magma with a ˜64-65 wt % SiO2 melt at 980°C and a NNO oxygen fugacity. We conclude that the andesitic and dacitic magmas are from separate magma storage regions (at >7 km and ˜2.4 km) due to differences in the bimodal whole rock, matrix glass, and phenocryst compositions and the presence or absence of stable hornblende. The time involved from the mixing event through the eruption is limited to a period of 4-5 days based on Fe-Ti oxide reequilibration, phenocryst growth rates, and hornblende breakdown. The eruption sequence is interpreted as having been initiated by an injection of the 1060±15°C andesitic magma into the ˜980°C (>7 km) andesite storage region. The mixed andesitic magma then intersected a shallow, ˜2.4 km, dacitic storage system on its way toward the surface. The eruption became more dacitic over time, and the final products some show evidence of partial reequilibration between the andesite and dacite.

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

NASA Astrophysics Data System (ADS)

Zoheir, Basem A.; Akawy, Ahmed

2010-06-01

Gold mineralisation at the Abu Marawat mine, central Eastern Desert of Egypt, is related to a system of massive and sheared, milky quartz veins cutting a sequence of Neoproterozoic island arc metavolcanic/volcaniclastic rocks and related banded iron formation (BIF). Sulphide-bearing quartz veins and related hydrothermal breccia bodies display a range of textures including sheared, boudinaged and recrystallised quartz, open space filling and microbreccia. These variable textures imply a complex history of crack-seal mechanism characterising the relation between mineral deposition and a major N-S-trending shear zone, during a late brittle-ductile deformation event which affected the area at about 550 Ma. Gold-base metal mineralisation is associated with brecciation and fracturing of the iron ore bands, close to silicified shears and related quartz veins. The auriferous quartz lodes are characterised by the occurrence of visible pyrite-chalcopyrite ± pyrrhotite ± sphalerite ± galena mineralisation. Gold is refractory in pyrite and chalcopyrite, but rare visible gold/electrum and telluride specks were observed in a few samples. Hydrothermal alteration includes pervasive silicification, pyritisation, sericitisation, carbonatisation confined to a delicate set of veins and altered shears, and a more widespread propylitic alteration assemblage (quartz + chlorite + pyrite + calcite ± epidote). Fluid inclusion petrography and microthermometric studies suggest heterogeneous trapping of a low-salinity (1.4-6.7 wt.% eq. NaCl) aqueous solution and a carbonic fluid. Evidence for fluid immiscibility during ore formation includes variable liquid/vapour ratios in inclusions along individual trails and bulk inclusion homogenisation into liquid and occasionally to vapour at comparable temperatures. The trapping conditions of intragranular aqueous-carbonic inclusions approximate 264-378 °C at 700-1300 bar. Similar temperature estimates have been obtained from Al-in-chlorite geothermometry of chlorite associated with sulphides in the mineralised quartz veins. Fracturing enhanced fluid circulation through the wallrock and related BIF, allowing reaction of the S-bearing ore fluid with iron oxides. This caused pyrite formation and concomitant Au precipitation, enhanced by fluid immiscibility as H 2S partitioned preferentially into the carbonic phase. The ore fluids may have originated from granitoid intrusions (likely the post-Hammamat felsites, whereas gold and base metals might have been leached from the Abu Marawat basic metavolcanics.

Mantle to Surface Fluid Transfer Above a Flat Slab Subduction Zone: Isotopic Evidence from Hot Springs in the Cordillera Blanca, Peru

NASA Astrophysics Data System (ADS)

Newell, D. L.; Jessup, M. J.; Hilton, D. R.; Shaw, C. A.; Hughes, C. A.

2015-12-01

Thermal springs in the Cordillera Blanca, Peru, provide geochemical evidence for deeply circulated hydrothermal fluids that carry significant mantle-derived helium. The Cordillera Blanca is a ~200 km-long NNW-SSE trending mountain range in the Peruvian Andes located above an amagmatic flat-slab subduction segment. The west side of the range is bounded by the Cordillera Blanca detachment that preserves a progression of top to the west ductile shear to brittle normal faulting since ~5 Ma. We report aqueous and stable isotope geochemical results from fluid and gas samples collected in 2013 and 2015 from 13 hot springs emanating from the Cordillera Blanca detachment and associated hanging wall faults. Most springs are vigorously bubbling (degassing), and range in temperature, pH, and conductivity from 17-89 °C, 5.95-8.87, and 0.17-21.5 mS, respectively. The hottest springs issue directly from the northern segment of the detachment. Geochemically, springs are CO2-rich, alkaline-chloride to alkaline-carbonate waters, with elevated trace metal contents including Fe, Cu, As, Zn, Sb, and Tl. Notably, As contents are ≤11 ppm, indicating that thermal waters may be adversely impacting local water quality. Water δ18O and δD, trends in elemental chemistry, and cation geothermometry collectively demonstrate mixing of hot (200-260 °C) saline fluid with cold meteoric recharge along the fault. Helium isotope ratios (3He/4He) for dissolved gases in the hot springs range from 0.62 to 1.98 RC/RA, indicating the presence of ~25% mantle-derived helium, assuming mixing of an asthenospheric end-member with the crustal helium reservoir. CO2/3He and carbon stable isotope ratios indicate a carbon source derived from mixing of crustal sources with minor mantle carbon. Overall, the volatile signature overlaps with orogen-wide datasets where crustal overprinting has modified mantle contributions at active arc volcanoes. Given the long duration since active magmatism in the Cordillera Blanca region, we suggest that mantle helium was mobilized from the continental mantle-lithosphere by metasomatic fluids derived from slab dehydration. These spring data thus reveal a mantle to surface connection and highlight the role of detachment faults in compressional orogens for fluid transfer in the crust.

Mixing of Magmatic Volatiles With Meteoric Groundwater in the Summit of Kilauea Volcano, Hawaii

NASA Astrophysics Data System (ADS)

Hurwitz, S.; Goff, F.; Janik, C. J.; Evans, W. C.; Counce, D. A.; Sorey, M. L.; Ingebritsen, S. E.

2001-12-01

Water samples were collected from the only deep well (Keller Well-NSF Well) on the summit of Kilauea volcano, Hawaii. The well was drilled in 1973 to a depth of 1262 m, but sat idle until 1998 when a drilling rig was used to remove mud and renew access to the hydrothermal system at a location very close to summit fumarolic activity. The chemistry and isotopic composition of fluid samples collected in 1998-2001 differ significantly from those of samples collected before 1998 and reported in previous studies. The water from the well is rich in sulfate and has a near-neutral pH. The major element chemistry differs significantly from seawater composition and from that of hydrothermal fluids from Kilauea's east rift zone. The well water has a low chloride concentration relative to typical magmatic-hydrothermal fluids and a high sulfate to bicarbonate ratio (approximately 4:1). Based on the S/Cl mass ratio and on carbon and helium isotopes in the well fluids, summit fumaroles and the parental Kilauea magma, we conclude that the hydrothermal fluids sampled from the well formed by condensation of magmatic volatiles into shallow, mainly meteoric groundwater. The oxygen and deuterium isotopic composition indicate that the meteoric component was recharged on the eastern margin of the caldera. Steam condensation and gas dissolution beneath the crater formed an acidic fluid that dissolved the host basalt at high temperatures. The hydrothermal fluid was then modified by cooling and precipitation of secondary minerals along a flow path away from the crater towards the well. Geochemical modeling based on fluid chemistry and geothermometry suggests that the well fluids equilibrated with an assemblage of secondary minerals at temperatures between 90 and 140oC. The C/S ratios in the well water, the parental magma, and the gas plume emanating from the caldera indicate that most of the sulfur degassed from the magma is scrubbed by groundwaters beneath the summit. However, based on the mean sulfate concentration in the well water and on the estimated mean annual water recharge in the caldera region, we conclude that the sulfate concentration in groundwater beneath Kilauea's summit must be an order of magnitude higher than that found in the well water.

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

NASA Astrophysics Data System (ADS)

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

2017-12-01

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

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

NASA Astrophysics Data System (ADS)

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

2017-04-01

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

Washington Geothermal Play Fairway Analysis Heat, Permeability, and Fracture Model Data

DOE Data Explorer

Steely, Alex; Forson, Corina; Cladouhos, Trenton; Swyer, Mike; Davatzes, Nicholas; Anderson, Megan; Ritzinger, Brent; Glen, Jonathan; Peacock, Jared; Schermerhorn, William

2017-12-07

This submission contains raster and vector data for the entire state of Washington, with specific emphasis on the three geothermal play fairway sites: Mount St. Helens seismic zone (MSHSZ), Wind River valley (WRV), and Mount Baker (MB). Data are provided for 3 major geothermal models: heat, permeability, and fluid-filled fractures, and an additional infrastructure model. Both of the permeability and fluid-filled-fracture models are produced at 200 m and at 2 km depths; the heat model is only produced at the 200 m depth. Values are provided for both model favorability and model confidence. A combined model at 200m and 2 km depths is provided for favorability, confidence, and exploration risk. Raster data are provided in GeoTiff format and have a statewide coverage. Cell size is 104.355 ft; file type is unsigned 8-bit integer (0-255); 0 represents no favorability or confidence; 255 represents maximum favorability or confidence. The NAD83(HARN)/Washington South (ftUS) projection is used (EPSG:2927). Vector data are provided in shapefile or comma-delimited text file formats. Geographic coordinates, where provided, are in WGS84. A readme file accompanies each folder and provides an overview and description of the enclosed data. The heat model combines 5 intermediate raster layers (which are included in the download package): temperature gradient wells, young volcanic vents, hot springs, young intrusive volcanic rocks, and geothermometry. The permeability model combines 8 intermediate raster layers: density of mapped faults, 2D dilation tendency of mapped faults, 2D slip tendency of mapped faults, seismicity, 3D dilation tendency, 3D slip tendency, 3D maximum coulomb shear stress, and 3D slip gradients. The fluid-filled fracture model combines up to 4 intermediate rasters: resistivity from magneto-telluric 3D inversions, seismicity, Vp/Vs anomalies from passive seismic tomography, and Vs anomalies from ambient-noise tomography. A statewide infrastructure model is also provided that formalizes land-use constraints and restrictions relevant for geothermal prospecting and development. This model combines 10 intermediate rasters: areas off limits to drilling, existing or proposed geothermal leases, DNR-owned land, land-use restrictions along the Columbia River Gorge, areas inundated by water, availability of potential process water, proximity to existing roads, proximity to transmission lines, distance from urban areas, and snow-related elevation restrictions. Supporting vector data for the development of each raster layer is provided. For details on the areas of interest and modeling process please see the 'WA_State_Play_Fairway_Phase_2_Technical_Report' in the download package.

Zr-in-rutile resetting in aluminosilicate bearing ultra-high temperature granulites: Refining the record of cooling and hydration in the Napier Complex, Antarctica

NASA Astrophysics Data System (ADS)

Mitchell, Ruairidh J.; Harley, Simon L.

2017-02-01

The relative validity and closure temperature of the Zr-in-rutile thermometer for recording UHT metamorphism are process dependent and hotly debated. We present an integrated petrological approach to Zr-in-rutile thermometry including phase equilibrium (pseudosection) modelling in complex chemical systems with updated mineral a-X models and systematic in-situ microanalysis of rutile. This study is centred on high-pressure rutile bearing UHT granulites from Mt. Charles, Napier Complex, Antarctica. P-T phase equilibrium modelling of two garnet bearing granulites (samples 49677, 49701) constrains an overall post-peak near isobaric cooling (IBC) evolution for the Napier Complex at Mt. Charles; from 14 kbar, 1100 °C with moderate decompression to 11 kbar, 800-900 °C. Local hydration on cooling over this temperature range is recorded in a kyanite bearing granulite (sample 49688) with an inferred injection of aqueous fluid equivalent to up to 9 mol% H2O from T-MH2O modelling. Further late stage cooling to < 740 °C is recorded by voluminous retrograde mica growth and partial preservation of a ky-pl-kfs-bt-liq bearing equilibrium assemblage. Overall, Zr-in-rutile temperatures at 11 kbar (Tomkins et al., 2007) are reset to between 606 °C and 780 °C across all samples, with flat core-rim Zr concentration profiles in all rutiles. However, zircon precipitates as inclusions, needle exsolutions, or rods along rutile grain boundaries are recrystallised from rutiles in qz/fsp domains. Reintegrating the Zr-in-rutile concentration 'lost' via the recrystallisation of these zircon precipitates (e.g. Pape et al., 2016) can recover maximum concentrations of up to 2.2 wt% and thus maximum peak temperatures of 1149 °C at 11 kbar. Rutile Nb-Ta signatures and rounded rutile grains without zircon precipitates in hydrated mica domains in sample 49688 provide evidence for fluid-mediated mobility of Zr and Nb during retrograde cooling in hydrated lithologies. Aqueous fluid supplemented excess H2O liberated by melt crystallisation, interacting with rutile on cooling of sample 49688 to reset Zr-in-rutile temperatures (606-780 °C) at the Mt. Charles locality. The wide range of geochemical and petrological characteristics of Napier Complex rutile highlights that Zr-in-rutile reintegration and a broad petrological approach are required for successful interpretation of Zr-in-rutile geothermometry for long-lived regional UHT metamorphism.

Oxygen Isotopes and the Cooling History of the Mount Barcroft Area, Central White Mountains, Easternmost California

NASA Astrophysics Data System (ADS)

Ernst, W. G.; Rumble, D.

2001-12-01

The White-Inyo Range + Owens Valley marks the western limit of the Basin and Range province, directly east of the Sierra Nevada. At Mount Barcroft, mid-Mesozoic, alkaline, bimodal White Mountain Peak metavolcanic + metaclastic rocks on the N are separated from Lower Cambrian siliciclastic + carbonate metasedimentary strata on the S by the NE-trending Middle Jurassic Barcroft mafic granodioritic pluton. It consists of mineralogically/chemically intergradational gabbro/diorite, granodiorite, metadiorite, and alaskite. Eastward, the section is intruded by the Late Cretaceous, ternary-minimum McAfee Creek Granite. Ignoring altered dikes, bulk-rock analyses of plutonic rocks indicate that metaluminous, I-type rocks of the Barcroft comagmatic suite possess an av(12) d18O value of 7.5. Slightly peraluminous, apparently S-type granitic rocks sensu stricto of the McAfee Creek series have an av(8) d18O value of 8.6. Evidence is lacking for large-scale bulk-rock interaction with near-surface waters, suggesting intermediate crustal depths of intrusion and cooling for these plutons. Coexisting Barcroft minerals exhibit consistent oxygen isotopic partitioning from high to low d18O in the sequence quartz > plagioclase > K-feldspar >> amphibole = biotite. Wall-rock quartz and biotite are richer in 18O than analogous phases in the plutonic rocks, and show slightly greater fractionations than igneous counterparts. Along its borders, late-stage exchange with heated aqueous fluids, derived from recrystallized wall rocks due to emplacement of the Middle Jurassic magma, increased 18O/16O ratios of dikes, and some Barcroft igneous plagioclase and subsolidus tremolite-actinolite. Oxygen isotope geothermometry for Barcroft quartz-amphibole and quartz-biotite pairs yields broadly similar temperatures; the combined average of 13 pairs is 519oC. A single quartz-biotite pair analyzed from a Lower Cambrian quartzite within the inner metamorphic aureole of the Barcroft pluton yields a temperature of 511oC, in agreement with values based on wall-rock metamorphic parageneses. Barcroft quartz, feldspars, biotite, and clinoamphiboles were subjected to exchange with deuteric fluid, and re-equilibrated under subsolidus conditions. Quartz-plagioclase pairs from two Barcroft granodiorites possess similar temperatures of 519 and 515oC, so also re-equilibrated at subsolidus temperatures. Areal distributions for quartz-plagioclase, quartz-clinoamphibole, and quartz-biotite pairs reveal that annealing temperatures are lowest in axial portions of the Barcroft granodioritic pluton. Late Cretaceous emplacement of the McAfee Creek Granite had little effect on d18O values of Barcroft minerals and bulk rocks.

Geochemical and isotopic evidence for the petrogenesis and emplacement tectonics of the Serra dos Órgãos batholith in the Ribeira belt, Rio de Janeiro, Brazil

NASA Astrophysics Data System (ADS)

Machado, Rômulo; Philipp, Ruy Paulo; McReath, Ian; Peucat, Jean Jacques

2016-07-01

The Serra dos Órgãos batholith in the State of Rio de Janeiro (Brazil) is a NE-SW-trending elongated body that occupies ca. 5000 km2 in plan view. It is a foliated intrusion, especially at its borders and is crosscut by syn-magmatic shear zones, with foliations that are moderately-to steeply-dipping to the northwest and moderately-to shallow-dipping in the center and to the southeast, in a configuration of a large laccolith. It was emplaced between 560 and 570 Ma, during an extensional episode that was part of a series of events that comprise the Brasiliano Orogeny in SE Brazil, and which includes deformation, metamorphism and granite intrusion during the interval between 630 and 480 Ma. The two main rock types in the batholith are biotite-hornblende monzogranite, and biotite leucogranite, with subordinate tonalite, granodiorite, diorite, quartz diorite (enclaves), aplite and pegmatite. Harker-type diagrams help show two rock groups with similar trends of evolution: a dioritic and a granitic. The first one is tholeiitic, whereas the second is calc-alkaline, with medium-to high-K calc-alkaline affinity and metaluminous to slightly peraluminous character. In both groups strong decrease in Al2O3, MgO, FeOT and CaO relative to silica contents are observed, which is compatible with trends of fractional crystallization involving clinopyroxene and/or hornblende, plagioclase, opaque minerals, apatite, microcline and biotite. The Sr and Nd isotopic data suggest recycling of a Paleoproterozoic crust as an important petrological process to generate the batholith rocks. Geothermometry (amphibole composition) and geobarometry (saturation in zircon and apatite) indicate that most of the batholith solidified at mid to lower crustal levels at about 750 °C and between 5 and 5.5 kbar. We consider that Serra dos Órgãos crustal protoliths underwent melting caused by the interaction with hotter mafic magma at the base of the crust. These two magmas, with distinct initial compositions and rheology, probably underwent mixing and mingling. This process continued during the rise of the magma through the crust, which was accompanied by magmatic differentiation. The main feature that characterizes the post-collisional Serra dos Órgãos granite magmatism is the connection with high angle ductile shear zones of continental scale and presence to a greater or lesser extent of mafic magmas.

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.

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

NASA Astrophysics Data System (ADS)

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

2017-04-01

The Sabatini Volcanic District (SVD) hosts a hydrothermal reservoir heated by the post-magmatic activity that affected the peri-Tyrrhenian sector of central Italy, giving rise to a number of thermal and mineral discharges. In this study, a complete geochemical and isotopic dataset based on the composition of 215 water and 9 bubbling gases, collected from the eastern sector of this huge hydrothermal system, is reported. The main aims are to (i) investigate the fluid sources and the main chemical-physical processes controlling the fluid chemistry and (ii) construct a conceptual fluid circulation model to provide insights into the possible use(s) of the geothermal resource. The fluid discharges are fed by two main aquifers, characterized by: (1) a Ca-HCO3 to Ca(Na)-HCO3 composition, typical of a shallow hydrological circuit within volcanic and sedimentary formations, and (2) a Ca-HCO3(SO4) to Na(Ca)-HCO3(Cl) composition, produced by the interaction of CO2-rich fluids with Mesozoic and Triassic carbonate-evaporite rocks. A thick sequence of low-permeability volcanic products represents a physical barrier between the two fluid reservoirs. As commonly occurring in central-southern Italy, CO2 is mainly produced by thermo-metamorphic decarbonation within the carbonate-evaporite reservoir, with minor contribution of mantle CO2. A dominant crustal source is also indicated by the relatively low R/Ra values (0.07-1.04). Methane and light hydrocarbons are mostly thermogenic, whereas H2S derives from thermogenic reduction of the Triassic anhydrites. Slightly positive 15N/14N values suggest minor N2 contribution from deep sedimentary sources. On the whole, a comparison of these geochemical features with those of the thermal fluids from the western portion of SVD highlights an eastward increasing influence of the shallow aquifer on the deep-originated fluids, likely caused by the proximity of the Apennine range from where the meteoric water, recharging the hydrothermal system, permeate. Accordingly, gas geothermometry in the CH4-CO2-H2 and H2S-CO2-H2 systems suggests equilibrium temperatures <200 °C, i.e. significantly lower than those measured in fluids from deep geothermal wells (300 °C). Although mitigated by the short distance from the Apennine range, the thermal anomaly recognized by fluid geochemistry in the eastern SVD makes this area suitable for direct exploitation of the geothermal resource.

Rapid thermal rejuvenation of high-crystallinity magma linked to porphyry copper deposit formation; evidence from the Koloula Porphyry Prospect, Solomon Islands

NASA Astrophysics Data System (ADS)

Tapster, S.; Condon, D. J.; Naden, J.; Noble, S. R.; Petterson, M. G.; Roberts, N. M. W.; Saunders, A. D.; Smith, D. J.

2016-05-01

Magmas containing the components needed to form porphyry copper deposits are relatively common within arcs, yet mineralising events are uncommon within the long-lived magmatic systems that host them. Understanding what causes the transition from barren to productive intrusions is critical to the development of conceptual deposit models. We have constrained the tempo of pre- and syn-mineralisation magmatic events in relationship to the thermal evolution of the plutonic body that underlies one of the world's youngest exposed plutonic-porphyry systems, the Inamumu Zoned Pluton, Koloula Porphyry Prospect, Solomon Islands. High precision ID-TIMS U-Pb dates of texturally and chemically characterised zircons indicate pluton emplacement over <150 kyr was superseded after ca. 50 kyr by two discrete episodes of mineralising porphyritic melt emplacement. Their associated hydrothermal systems initiated within ca. 30 kyrs of each other. Zircon populations within evolved intrusions contain resorbed cores that were recycled from the deeper magmatic system, yet their youngest dates are statistically indistinguishable from those yielded by crystals lacking resorption. Comparisons of Ti-in-zircon proxy temperatures, modelled zircon saturation temperatures and temperature-crystallinity relationships suggest that prior to being heated and emplaced within the shallow level pluton, magmas were stored at depth in a high-crystallinity (>50% crystals) state, past the point of rheological lock-up. We estimate that thermal rejuvenation of the deeper high-crystallinity magma and generation of a mobile melt fraction may have occurred ≤10 kyr before its transport and emplacement within the porphyry environment. The underlying pluton likely cooled and returned to high-crystallinity states prior to subsequent remobilisation-emplacement events. Titanium-in-zircon geothermometry and whole-rock geochemistry suggest pre-mineralisation intrusions were remobilised by mixing of a silicic magma with a high-temperature, less-evolved melt. In contrast, syn-mineralisation melts were most likely remobilised by the percolation of hot volatiles exsolved from contemporaneous less-evolved intrusions cooling beneath the crystalline silicic magma. The evidence for the rapid thermal rejuvenation and long term storage of highly crystalline silicic magmas is consistent with previous studies that indicate two components of exsolved volatiles contribute to ore forming fluids. We conclude that the liberation of crystal-rich porphyry copper deposit forming magmas, and the addition of the chemical components required for ore formation, are intrinsically linked to the volatiles released during the recharge of less-evolved melt into a highly crystalline silicic magma.

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

FeTi oxide mineralogy and the origin of normal and reverse remanent magnetization in dacitic pumice blocks from Mt. Shasta, California

USGS Publications Warehouse

Lawson, C.A.; Nord, G.L.; Champion, D.E.

1987-01-01

Detailed mineralogical analyses and rock magnetic experiments have made it possible to directly identify the FeTi oxide phases responsible for the normal and reverse magnetic components of two dacitic pumice blocks from Mt. Shasta, California. Both samples contain a normal component carried by 100 ??m size multi-domain (MD) titanomagnetite (Usp11-24). One sample also contains a second normal component carried by < 10 ??m size pseudo-single domain (PSD) or single domain (SD) Ti-free magnetite (Usp1) found in the dacitic glass. The MD titanomagnetite and PSD or SD magnetite dominate the strong field magnetic signal, but only the PSD or SD magnetite has any influence on the remanence signal. Unlike the strong field signal, the remanence signal of both samples is dominated by a reverse NRM component. This reverse component is carried by 100 ??m size ferrian ilmenite (Ilm53-65). The compositions of the ilmenites in both samples are within the range of compositions (Ilm50-75) known to have the ability to acquire self-reversing thermoremanent magnetizations (TRM). The results of the Lowric-Fuller test indicate that the remanence signal is dominated by PSD or SD carriers. Because one sample contains only large MD titanomagnetite and no SD Ti-free magnetite (in addition to ferrian ilmenite), the ferrian ilmenite must be a PSD or SD carrier. Oxide and pyroxene geothermometry indicate the FeTi oxides in the pumice crystallized at temperatures between 880 and 945??C. This temperature range is within the disordered region of the ilmenite-hematite phase diagram for Ilm53-65. Previous work on synthetic Ilm70 and Ilm80 has shown that cooling through the order-disorder transition into the ordered region develops a transformation-induced microstructure consisting of cation-ordered domains with disordered domain boundaries. An Ilm58-59 grain from one of the Mt. Shasta samples was examined in the transmission electron microscope and was found to contain 100-200 A?? diameter cation-ordered domains. These domains arose during cooling through the transition temperature, which is estimated at 800??C for Ilm58-59. The presence of the disordered domain boundaries provides an explanation for the magnetic behavior of the ferrian ilmenite. (1) The disordered boundaries are the higher Curie point phase necessary for the operation of the self-reversal mechanism. (2) The disordered domain boundaries either inhibit the formation of magnetic domain walls or restrict magnetic domain wall movement accounting for the PSD or SD behavior of the ferrian ilmenite. ?? 1987.

Cooling and crystallization of lava in open channels, and the transition of Pāhoehoe Lava to 'A'ā

NASA Astrophysics Data System (ADS)

Cashman, Katharine V.; Thornber, Carl; Kauahikaua, James P.

Samples collected from a lava channel active at Kīlauea Volcano during May 1997 are used to constrain rates of lava cooling and crystallization during early stages of flow. Lava erupted at near-liquidus temperatures ( 1150 °C) cooled and crystallized rapidly in upper parts of the channel. Glass geothermometry indicates cooling by 12-14 °C over the first 2km of transport. At flow velocities of 1-2m/s, this translates to cooling rates of 22-50 °C/h. Cooling rates this high can be explained by radiative cooling of a well-stirred flow, consistent with observations of non-steady flow in proximal regions of the channel. Crystallization of plagioclase and pyroxene microlites occurred in response to cooling, with crystallization rates of 20-50% per hour. Crystallization proceeded primarily by nucleation of new crystals, and nucleation rates of 104/cm3s are similar to those measured in the 1984 open channel flow from Mauna Loa Volcano. There is no evidence for the large nucleation delays commonly assumed for plagioclase crystallization in basaltic melts, possibly a reflection of enhanced nucleation due to stirring of the flow. The transition of the flow surface morphology from pāhoehoe to 'a'ā occurred at a distance of 1.9km from the vent. At this point, the flow was thermally stratified, with an interior temperature of 1137 °C and crystallinity of 15%, and a flow surface temperature of 1100 °C and crystallinity of 45%. 'A'ā formation initiated along channel margins, where crust was continuously disrupted, and involved tearing and clotting of the flow surface. Both observations suggest that the transition involved crossing of a rheological threshold. We suggest this threshold to be the development of a lava yield strength sufficient to prevent viscous flow of lava at the channel margin. We use this concept to propose that 'a'ā formation in open channels requires both sufficiently high strain rates for continued disruption of surface crusts and sufficient groundmass crystallinity to generate a yield strength equivalent to the imposed stress. In Hawai'i, where lava is typically microlite poor on eruption, these combined requirements help to explain two common observations on 'a'ā formation: (a) 'a'ā flow fields are generated when effusion rates are high (thus promoting crustal disruption); and (b) under most eruption conditions, lava issues from the vent as pāhoehoe and changes to 'a'ā only after flowing some distance, thus permitting sufficient crystallization.

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

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

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

1980-06-01

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

The growth history of the Lago Della Vacca (Southern Adamello Massive, Italy) intrusion from field observations, thermal and rheological modelling

NASA Astrophysics Data System (ADS)

Rust, A.; Annen, C.; Blundy, J. D.; Caricchi, L.

2010-12-01

The Lago Della Vacca granitoid is an intrusive body emplaced at about 4-6 km in up to 1 My. The core of the body is characterised by the presence of dyke-like structures, enclave-swarms and randomly distributed enclaves, which appear undeformed. Enclaves become oblate with the short axis perpendicular to the foliation, which, in turn follows the margin of the plutonic body (John and Blundy, 1993). Geothermometry and experimental data have been used to constrain the temperature of injection of the mafic component (1273-1323 K), the temperature of the host granitic magma (1173-1223), and to characterise the evolution of crystallinity with temperature for both magmas (Blundy and Sparks, 1992). Based on these data thermal and rheological modelling have been combined to interpret the growth and deformation history of the Lago della Vacca intrusive body. The pluton was modeled as a series of incrementally emplaced nested cylinders with 1D-cylindrical conductive heat transfer. The evolution of temperature and melt fraction distribution in the pluton and country rock were determined and used as input parameters for the rheological modelling. The rheology of each magma depends on the viscosity of the melt and, more importantly, on crystallinity. Field observations suggest that the mafic magma was injected as dykes. Their partial or total disaggregation produced mafic enclaves. The presence of randomly distributed enclaves in the core of Lago Della Vacca body indicates that convection was active in this portion of the intrusion. The undeformed nature of the enclaves in this region also implies that the contrast in temperature between host magma and mafic material produced a sudden (hours) rheological inversion with the mafic magma becoming more viscous than the felsic end-member. In these conditions, the enclaves would be transported passively by the felsic-host without suffering any substantial deformation. Thermal modelling indicates that to maintain the core of the pluton above solidus temperature between injections requires either fast emplacement or high initial temperatures of the country rocks. The latter is unlikely for emplacement depths of 4-6 km and as a consequence we infer duration of emplacement up to few hundred thousand years. The wider range of zircon ages may reflect combined intrusion and thermal relaxation times. The extremely flattened enclaves at the rim of the pluton are the result of deformation at lower temperature as the core inflates. As magmas cool the crystallinity of host become as high as the enclaves, resulting in a small viscosity contrast between them, which can be seen as a Window of Mutual Deformability (WMD). Further straining results in a homogeneous deformation and flattening of the enclaves parallel to the margins.

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

NASA Astrophysics Data System (ADS)

Jimenez, A.

2012-04-01

Sulfur isotope study of the Velardeña skarn (Zn-Pb), Durango, Mexico Abigail Jimenez-Franco1*, Pura Alfonso Abella2, Carles Canet3, Eduardo González-Partida4 1 Posgrado en Ciencias de la Tierra, Universidad Nacional Autónoma de México, Ciudad Universitaria, Delegación Coyoacán, 04510 México D.F., Mexico 2 Departament d'Enginyeria Minera i Recursos Naturals, Universitat Politècnica de Catalunya, Av de Les Bases de Manresa 61-73, 08242 Manresa. 3Instituto de Geofísica, Universidad Nacional Autónoma de México, Ciudad Universitaria, Delegación Coyoacán, 04510 México D.F., Mexico 4Centro de Geociencias, Universidad Nacional Autónoma de México, Campus Juriquilla, Boulevard Juriquilla 3001, 76230 Santiago de Querétaro, Qro., Mexico The Velardeña mining district is located in north-eastern part of the state of Durango, in northern of Mexico. The ore deposit is a lead-zinc, garnet-rich skarn developed at the contact between granite porphyry dikes (Eocene) and well-laminated limestones with interbedded chert (Albian-Cenomanian). A study of sulfur isotopes has been carried out in various sulfide minerals of the ores of Velardeña, in order to: (a) constrain the possible sources of sulfur and, therefore, better understand the sulfide mineralizing processes, and (b) to estimate the temperature of the ore-forming stage of the skarn. Sulfur isotope analyses were performed in 21 pure fractions of sulfide minerals of the ore mineralization (pyrite, chalcopyrite, sphalerite and galena). The mineral separation was performed using a series of sieves, and the purity of the samples was verified under a binocular microscope. Isotopic analyses were done on a Finnigan MAT Delta C flow elemental analyzer coupled to a TC-EA, according with the method of Giesemann et al. (1974). The δ34S values of the analyzed sulfides range mostly between -0.6 and +2.6 ‰ (relative to the CDT standard). These values are indicative of a magmatic source of sulfur. A single analysis falls outside the common range of magmatic sulfur; it corresponds to a sphalerite crystal with δ34S of -3.9 ‰. This negative value could be explained by the incorporation of sulfur leached from the sedimentary host rocks. Pyrite and galena in paragenesis were analyzed from one sample (CO-9F); the isotope fractionation equation of Ohmoto and Rye (1979) was applied for geothermometry purposes. This calculation yields a temperature of 346° ±25° C, from fractionation Δpyrite-galena of 2.66 ‰.

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

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

Probing the structure of the sub-Salinia mantle lithosphere using spinel lherzolite xenoliths from Crystal Knob, Santa Lucia Range, California

NASA Astrophysics Data System (ADS)

Quinn, D. P.; Saleeby, J.; Ducea, M. N.; Luffi, P. I.

2013-12-01

We present the first petrogenetic analysis of a suite of peridotite xenoliths from the Crystal Knob volcanic neck in the Santa Lucia Range, California. The neck was erupted during the Plio-Pleistocene through the Salinia terrane, a fragment of the Late Cretaceous southern Sierra-northwest Mojave supra-subduction core complex that was displaced ~310 km in the late Cenozoic along the dextral San Andreas fault. The marginal tectonic setting makes these xenoliths ideal for testing different models of upper-mantle evolution along the western North American plate boundary. Possible scenarios include the early Cenozoic underplating of Farallon-plate mantle lithosphere nappes (Luffi et al., 2009), Neogene slab window opening (Atwater and Stock, 1998), and the partial subduction and stalling of the Monterey microplate (Pisker et al., 2012). The xenoliths from Crystal Knob are spinel lherzolites, which sample the mantle lithosphere underlying Salinia, and dunite cumulates apparently related to the olivine-basalt host. Initial study is focused on the spinel lherzolites: these display an allotriomorphic granular texture with anisotropy largely absent. However, several samples exhibit a weak shape-preferred orientation in elongate spinels. Within each xenolith, the silicate phases are in Fe-Mg equilibrium; between samples, Mg# [molar Mg/(Mg+Fe)*100] ranges from 87 to 91. Spinels have Cr# [molar Cr/(Cr+Al)*100] ranging from 10 to 27. Clinopyroxene Rb-Sr and Sm-Nd radiogenic isotope data show that the lherzolites are depleted in large-ion lithophile (LIL) elements, with uniform enrichment in 143Nd (ɛNd from +10.3 to +11.0) and depletion in 87Sr (87/86Sr of .702). This data rules out origin in the continental lithosphere, such as that observed in xenoliths from above the relict subduction interface found at at Dish Hill and Cima Dome in the Mojave (Luffi et al., 2009). The Mesozoic mantle wedge, which is sampled by xenoliths from beneath the southern Sierra Nevada batholith (Ducea and Saleeby, 1998), is also ruled out as a source locale. The isotopic data are consistent with oceanic mantle originating from either the Farallon plate (underplated during Paleocene shallow subduction) or the Monterey plate (partially subducted during the Miocene). Ascended asthenosphere, presumably of slab-window origin, is also a possible source. Pyroxene Ca-Mg exchange geothermometry is in progress and will enable thermal modeling and comparisons with contemporary heat flow data. These results, along with trace-element analysis of clinopyroxene crystals, will be used to distinguish between the possible sources of LIL-depleted mantle in the sub-Salinia mantle lithosphere. The full petrogenetic survey of these xenoliths adds a distal constraint to the makeup of the mantle lithosphere beneath the western North American margin.

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.

Scrubbing masks magmatic degassing during repose at Cascade-Range and Aleutian-Arc volcanoes

USGS Publications Warehouse

Symonds, Robert B.; Janik, C.J.; Evans, William C.; Ritchie, B.E.; Counce, Dale; Poreda, R.J.; Iven, Mark

2003-01-01

Between 1992 and 1998, we sampled gas discharges from ≤173°C fumaroles and springs at 12 quiescent but potentially restless volcanoes in the Cascade Range and Aleutian Arc (CRAA) including Mount Shasta, Mount Hood, Mount St. Helens, Mount Rainier, Mount Baker, Augustine Volcano, Mount Griggs, Trident, Mount Mageik, Aniakchak Crater, Akutan, and Makushin. For each site, we collected and analyzed samples to characterize the chemical (H2O, CO2, H2S, N2, CH4, H2, HCl, HF, NH3, Ar, O2, He) and isotopic (δ13C of CO2, 3He/4He, 40Ar/36Ar, δ34S, δ13C of CH4, δ15N, and δD and δ18O of water) compositions of the gas discharges, and to create baseline data for comparison during future unrest. The chemical and isotopic data show that these gases contain a magmatic component that is heavily modified from scrubbing by deep hydrothermal (150° - 350°C) water (primary scrubbing) and shallow meteoric water (secondary scrubbing). The impact of scrubbing is most pronounced in gas discharges from bubbling springs; gases from boiling-point fumaroles and superheated vents show progressively less impact from scrubbing. The most effective strategies for detecting gas precursors to future CRAA eruptions are to measure periodically the emission rates of CO2 and SO2, which have low and high respective solubilities in water, and to monitor continuously CO2 concentrations in soils around volcanic vents. Timely resampling of fumaroles can augment the geochemical surveillance program by watching for chemical changes associated with drying of fumarolic pathways (all CRAA sites), increases in gas geothermometry temperatures (Mount Mageik, Trident, Mount Baker, Mount Shasta), changes in δ13C of CO2 affiliated with magma movement (all CRAA site), and increases in 3He/4He coupled with intrusion of new magma (Mount Rainier, Augustine Volcano, Makushin, Mount Shasta). Repose magmatic degassing may discharge substantial amounts of S and Cl into the edifices of Mount Baker and several other CRAA volcanoes that is trapped by primary and secondary scrubbing. The consequent acidic fluids produce ongoing alteration in the 0.2- to 3-km-deep hydrothermal systems and in fields of boiling-point fumaroles near the surface. Such alteration may influence edifice stability and contribute to the formation of more-hazardous cohesive debris flows. In particular, we recommend further investigation of the volume, extent, and hazards of hydrothermal alteration at Mount Baker. Other potential hazards associated with the CRAA volcano hydrothermal systems include hydrothermal eruptions and, for deeper systems intruded by magma, deep-seated edifice collapse.

Geochemical constraints on volatile sources and subsurface conditions at Mount Martin, Mount Mageik, and Trident Volcanoes, Katmai Volcanic Cluster, Alaska

NASA Astrophysics Data System (ADS)

Lopez, T.; Tassi, F.; Aiuppa, A.; Galle, B.; Rizzo, A. L.; Fiebig, J.; Capecchiacci, F.; Giudice, G.; Caliro, S.; Tamburello, G.

2017-11-01

We use the chemical and isotopic composition of volcanic gases and steam condensate, in situ measurements of plume composition and remote measurements of SO2 flux to constrain volatile sources and characterize subvolcanic conditions at three persistently degassing and seismically active volcanoes within the Katmai Volcanic Cluster (KVC), Alaska: Mount Martin, Mount Mageik and Trident. In situ plume measurements of gas composition were collected at all three volcanoes using MultiGAS instruments to calculate gas ratios (e.g. CO2/H2S, SO2/H2S and H2O/H2S), and remote measurements of SO2 column density were collected from Mount Martin and Mount Mageik by ultraviolet spectrometer systems to calculate SO2 fluxes. Fumaroles were directly sampled for chemical and isotopic composition from Mount Mageik and Trident. Mid Ocean Ridge Basalt (MORB)-like 3He/4He ratios ( 7.2-7.6 Rc/RA) within Mount Mageik and Trident's fumarole emissions and a moderate SO2 flux ( 75 t/d) from Mount Martin, combined with gas compositions dominated by H2O, CO2 and H2S from all three volcanoes, indicate magma degassing and active hydrothermal systems in the subsurface of these volcanoes. Mount Martin's gas emissions have the lowest CO2/H2S ratio ( 2-4) and highest SO2 flux compared to the other KVC volcanoes, indicative of shallow magma degassing. Geothermometry techniques applied to Mount Mageik and Trident's fumarolic gas compositions suggest that their hydrothermal reservoirs are located at depths of 0.2 and 4 km below the surface, respectively. Observations of an unusually reducing gas composition at Trident and organic material in the near-surface soils suggest that thermal decomposition of sediments may be influencing gas composition. When the measured gas compositions from Mount Mageik and Trident are compared with previous samples collected in the late 1990's, relatively stable magmatic-hydrothermal conditions are inferred for Mount Mageik, while gradual degassing of residual magma and contamination by shallow crustal fluids is inferred for Trident. The isotopic composition of volcanic gases emitted from Mount Mageik and Trident reflect mixing of subducted slab, mantle and crustal volatile sources, with organic sediment and carbonate being the predominant sources. Considering the close proximity of the target volcanoes in comparison with the depth to the subducted slab we speculate that Aleutian Arc volatiles are fed by a relatively homogeneous subducted fluid and that much of the apparent variability in volatile provenance can be explained by shallow crustal volatile sources and/or processes.

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

NASA Astrophysics Data System (ADS)

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

2016-04-01

In this Geothermal Play Fairways Analysis project we sought to develop new ways to analyze geologic, geochemical, and geophysical data to reduce the risk and increase the prospects of successful geothermal exploration and development. We collected, organized, and analyzed data from southwest New Mexico in the context of an integrated framework that combines the data for various signatures of a geothermal resource into a cohesive analysis of the presence of heat, fluid, and permeability. We incorporated data on structural characteristics (earthquakes, geophysical logs, fault location and age, basement depth), topographic and water table elevations, conservative ion concentrations, and thermal information (heat flow, bottom hole temperature, discharge temperature, and basement heat generation). These data were combined to create maps that indicate structural analysis, slope, geothermometry, and heat. We also mapped discharge areas (to constrain elevations where groundwater may be discharged through modern thermal springs or paleo-thermal springs) and subcrops: possible erosionally- or structurally-controlled breaches in regional-scale aquitards that form the basis of our hydrogeologic windows concept. These two maps were particularly useful in identifying known geothermal systems and narrowing the search for unknown geothermal prospects. We further refined the "prospectivity" of the areas within the subcrops and discharge areas by developing and applying a new method for spatial association analysis to data on known and inferred faults, earthquakes, geochemical thermometers, and heat flow. This new methodology determines the relationships of the location and magnitudes of observations of these data with known geothermal sites. The results of each of the six spatial association analyses were weighted between 0 and 1 and summed to produce a prospectivity score between 0 and 6, with 6 indicating highest geothermal potential. The mean value of prospectivity for all regions with positive prospectivity inside subcrops and discharge areas was 1.83 (standard deviation = 0.75), whereas this mean prospectivity for known geothermal sites was 3.07 (standard deviation = 0.90). These results suggest that our prospectivity analysis using our integrated framework and the hydrogeologic windows concept is useful for identifying known and potential geothermal resources. The prospectivity approach also substantially reduces the number of known geothermal resources per km2 (from 0.004 at prospectivity > 0 to 0.016 at prospectivity > 3), suggesting that limiting an exploration area to regions with high prospectivity scores could reduce exploration costs. Comparing this method to more simplistic methods revealed that this method consistently had a higher density of resources in the top quintile for prospectivity. Using our prospectivity map, we identified nine sites for further data collection and analysis: Rincon, Lordsburg, Mud Springs, Gillis Hot Well, Goodsight, Cliff-Riverside, Rio Salado/Lucero, and the Northern Little Florida Mountains.

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

USGS Publications Warehouse

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

2008-01-01

Talc, kerolite-smectite, smectite, chlorite-smectite and chlorite samples from sediments, chimneys and massive sulfides from six seafloor hydrothermal areas have been analyzed for mineralogy, chemistry and oxygen isotopes. Samples are from both peridotite- and basalt-hosted hydrothermal systems, and basaltic systems include sediment-free and sediment-covered sites. Mg-phyllosilicates at seafloor hydrothermal sites have previously been described as talc, stevensite or saponite. In contrast, new data show tri-octahedral Mg-phyllosilicates ranging from pure talc and Fe-rich talc, through kerolite-rich kerolite-smectite to smectite-rich kerolite-smectite and tri-octahedral smectite. The most common occurrence is mixed-layer kerolite-smectite, which shows an almost complete interstratification series with 5 to 85% smectitic layers. The smectite interstratified with kerolite is mostly tri-octahedral. The degree of crystal perfection of the clay sequence decreases generally from talc to kerolite-smectite with lower crystalline perfection as the proportion of smectite layers in kerolite-smectite increases. Our studies do not support any dependence of the precipitated minerals on the type/subtype of hydrothermal system. Oxygen isotope geothermometry demonstrates that talc and kerolite-smectite precipitated in chimneys, massive sulfide mounds, at the sediment surface and in open cracks in the sediment near seafloor are high-temperature (> 250????C) phases that are most probably the result of focused fluid discharge. The other end-member of this tri-octahedral Mg-phyllosilicate sequence, smectite, is a moderate-temperature (200-250????C) phase forming deep within the sediment (??? 0.8??m). Chlorite and chlorite-smectite, which constitute the alteration sediment matrix around the hydrothermal mounds, are lower-temperature (150-200????C) phases produced by diffuse fluid discharge through the sediment around the hydrothermal conduits. In addition to temperature, other two controls on the precipitation of this sequence are the silica activity and Mg/Al ratio (i.e. the degree of mixing of seawater with hydrothermal fluid). Higher silica activity favors the formation of talc relative to tri-octahedral smectite. Vent structures and sedimentary cover preclude complete mixing of hydrothermal fluid and ambient seawater, resulting in lower Mg/Al ratios in the interior parts of the chimneys and deeper in the sediment which leads to the precipitation of phyllosilicates with lower Mg contents. Talc and kerolite-smectite have very low trace- and rare earth element contents. Some exhibit a negative or flat Eu anomaly, which suggests Eu depletion in the original hydrothermal fluid. Such Eu depletion could be caused by precipitation of anhydrite or barite (sinks for Eu2+) deeper in the system. REE abundances and distribution patterns indicate that chlorite and chlorite-smectite are hydrothermal alteration products of the background turbiditic sediment. ?? 2007 Elsevier B.V. All rights reserved.

Assessing the isotopic evolution of S-type granites of the Carlos Chagas Batholith, SE Brazil: Clues from U-Pb, Hf isotopes, Ti geothermometry and trace element composition of zircon

NASA Astrophysics Data System (ADS)

Melo, Marilane G.; Lana, Cristiano; Stevens, Gary; Pedrosa-Soares, Antônio C.; Gerdes, Axel; Alkmin, Leonardo A.; Nalini, Hermínio A.; Alkmim, Fernando F.

2017-07-01

The Carlos Chagas batholith (CCB) is a very large ( 14,000 km2) S-type granitic body formed during the syn-collisional stage of the Araçuaí orogen (southeastern Brazil). Zircons extracted from the CCB record a wide range of U-Pb ages (from 825 to 490 Ma), indicating a complex history of inheritance, magmatic crystallization and partial melting during the evolution of the orogeny. Magmatic zircons (ca. 578-588 Ma) are marked by similar Hf isotope compositions and REE patterns to those of inherited cores (ca. 825-600 Ma), indicating that these aspects of the chemical signature of the magmatic zircons have likely been inherited from the source. The U-Pb ages and initial 176Hf/177Hf ratios from anatectic and metamorphic zircon domains are consistent with a two-stage metamorphic evolution marked by contrasting mechanisms of zircon growth and recrystallization during the orogeny. Ti-in-zircon thermometry is consistent with the findings of previous metamorphic work and indicates that the two metamorphic events in the batholith reached granulite facies conditions (> 800 °C) producing two generations of garnet via fluid-absent partial melting reactions. The oldest metamorphic episode (ca. 570-550 Ma) is recorded by development of thin anatectic overgrowths on older cores and by growth of new anatectic zircon crystals. Both domains have higher initial 176Hf/177Hf values compared to relict cores and display REE patterns typical of zircon that grew contemporaneously with peritectic garnet through biotite-absent fluid partial melting reactions. Hf isotopic and chemical evidences indicate that a second anatectic episode (ca. 535-500 Ma) is only recorded in parts from the CCB. In these rocks, the growth of new anatectic zircon and/or overgrowths is marked by high initial 176Hf/177Hf values and also by formation of second generation of garnet, as indicated by petrographic observations and REE patterns. In addition, some rocks contain zircon crystals formed by solid-state recrystallization of pre-existing zircon, which exhibit similar Hf isotope composition to those of inherited/magmatic core domains. The first anatectic event is interpreted as result of crustal thickening after the intrusion of the batholith. This introduced the batholith to a depth in excess of 30 km and produced widespread anatexis throughout the batholith. The second event was associated with asthenospheric upwelling during extensional thinning and gravitational collapse of the orogen, this produced anatexis in parts from the CCB that had been re-fertilized for anatexis by retrogression along shear zones following the first granulite facies event.

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.

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

NASA Astrophysics Data System (ADS)

Arcay, Diane

2017-08-01

The present study aims at better deciphering the different mechanisms involved in the functioning of the subduction interplate. A 2D thermo-mechanical model is used to simulate a subduction channel, made of oceanic crust, free to evolve. Convergence at constant rate is imposed under a 100 km thick upper plate. Pseudo-brittle and non-Newtonian behaviours are modelled. The influence of the subduction channel strength, parameterized by the difference in activation energy between crust and mantle (ΔEa) is investigated to examine in detail the variations in depth of the subduction plane down-dip extent, zcoup . First, simulations show that numerical resolution may be responsible for an artificial and significant shallowing of zcoup if the weak crustal layer is not correctly resolved. Second, if the age of the subducting plate is 100 Myr, subduction occurs for any ΔEa . The stiffer the crust is, that is, the lower ΔEa is, the shallower zcoup is (60 km depth if ΔEa = 20 kJ/mol) and the hotter the fore-arc base is. Conversely, imposing a very weak subduction channel (ΔEa > 135 J/mol) leads there to an extreme mantle wedge cooling and inhibits mantle melting in wet conditions. Partial kinematic coupling at the fore-arc base occurs if ΔEa = 145 kJ/mol. If the incoming plate is 20 Myr old, subduction can occur under the conditions that the crust is either stiff and denser than the mantle, or weak and buoyant. In the latter condition, cold crust plumes rise from the subduction channel and ascend through the upper lithosphere, triggering (1) partial kinematic coupling under the fore-arc, (2) fore-arc lithosphere cooling, and (3) partial or complete hindrance of wet mantle melting. zcoup then ranges from 50 to more than 250 km depth and is time-dependent if crust plumes form. Finally, subduction plane dynamics is intimately linked to the regime of subduction-induced corner flow. Two different intervals of ΔEa are underlined: 80-120 kJ/mol to reproduce the range of slab surface temperature inferred from geothermometry, and 10-40 kJ/mol to reproduce the shallow hot mantle wedge core inferred from conditions of last equilibration of near-primary arc magmas and seismic tomographies. Therefore, an extra process controlling mantle wedge dynamics is needed to satisfy simultaneously the aforementioned observations. A mantle viscosity reduction, by a factor 4-20, caused by metasomatism in the mantle wedge is proposed. From these results, I conclude that the subduction channel down-dip extent, zcoup , should depend on the subduction setting, to be consistent with the observed variability of sub-arc depths of the subducting plate surface.

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

USGS Publications Warehouse

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

2011-01-01

Large bulk-tonnage high-sulfidation gold deposits, such as Yanacocha, Peru, are the surface expression of structurally-controlled lode gold deposits, such as El Indio, Chile. Both formed in active andesite-dacite volcanic terranes. Fluid inclusion, stable isotope and geologic data show that lode deposits formed within 1500. m of the paleo-surface as a consequence of the expansion of low-salinity, low-density magmatic vapor with very limited, if any, groundwater mixing. They are characterized by an initial 'Sulfate' Stage of advanced argillic wallrock alteration ?? alunite commonly with intense silicification followed by a 'Sulfide' Stage - a succession of discrete sulfide-sulfosalt veins that may be ore grade in gold and silver. Fluid inclusions in quartz formed during wallrock alteration have homogenization temperatures between 100 and over 500 ??C and preserve a record of a vapor-rich environment. Recent data for El Indio and similar deposits show that at the commencement of the Sulfide Stage, 'condensation' of Cu-As-S sulfosalt melts with trace concentrations of Sb, Te, Bi, Ag and Au occurred at > 600 ??C following pyrite deposition. Euhedral quartz crystals were simultaneously deposited from the vapor phase during crystallization of the vapor-saturated melt occurs to Fe-tennantite with progressive non-equilibrium fractionation of heavy metals between melt-vapor and solid. Vugs containing a range of sulfides, sulfosalts and gold record the changing composition of the vapor. Published fluid inclusion and mineralogical data are reviewed in the context of geological relationships to establish boundary conditions through which to trace the expansion of magmatic vapor from source to surface and consequent alteration and mineralization. Initially heat loss from the vapor is high resulting in the formation of acid condensate permeating through the wallrock. This Sulfate Stage alteration effectively isolates the expansion of magmatic vapor in subsurface fracture arrays from any external contemporary hydrothermal activity. Subsequent fracturing is localized by the embrittled wallrock to provide high-permeability fracture arrays that constrain vapor expansion with minimization of heat loss. The Sulfide Stage vein sequence is then a consequence of destabilization of metal-vapor species in response to depressurization and decrease in vapor density. The geology, mineralogy, fluid inclusion and stable isotope data and geothermometry for high-sulfidation, bulk-tonnage and lode deposits are quite different from those for epithermal gold-silver deposits such as McLaughlin, California that formed near-surface in groundwater-dominated hydrothermal systems where magmatic fluid has been diluted to less than about 30%. High sulfidation gold deposits are better termed 'Solfataric Gold Deposits' to emphasize this distinction. The magmatic-vapor expansion hypothesis also applies to the phenomenology of acidic geothermal systems in active volcanic systems and equivalent magmatic-vapor discharges on the flanks of submarine volcanoes. ?? 2010.

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

NASA Astrophysics Data System (ADS)

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

2014-09-01

The Acoculco caldera has been recognized by the Mexican Federal Electricity Company (CFE) as a Hot Dry Rock Geothermal System (HDR) and could be a potential candidate for developing an Enhanced Geothermal System (EGS). Apart from hydrothermally altered rocks, geothermal manifestations within the Acoculco caldera are scarce. Close to ambient temperature bubbling springs and soil degassing are reported inside the caldera while a few springs discharge warm water on the periphery of the caldera. In this study, we infer the origin of fluids and we characterize for the first time the soil degassing dynamic. Chemical and isotopic (δ18O-δD) analyses of spring waters indicate a meteoric origin and the dissolution of CO2 and H2S gases, while gas chemical and isotopic compositions (N2/He, 3He/4He, 13C, 15N) reveal a magmatic contribution with both MORB- and arc-type signatures which could be explained by an extension regime created by local and regional fault systems. Gas geothermometry results are in agreement with temperature measured during well drilling (260 °C-300 °C). Absence of well-developed water reservoir at depth impedes re-equilibration of gases upon surface. A multi-gas flux survey including CO2, CH4 and H2S measurements was performed within the caldera. Using the graphical statistical analysis (GSA) approach, CO2 flux measurements were classified in two populations. Population A, representing 95% of measured fluxes is characterized by low values (mean: 18 g m- 2 day- 1) while the remaining 5% fluxes belonging to Population B are much higher (mean: 5543 g m- 2 day- 1). This low degassing rate probably reflects the low permeability of the system, a consequence of the intense hydrothermal alteration observed in the upper 800 m of volcanic rocks. An attempt to interpret the origin and transport mechanism of these fluxes is proposed by means of flux ratios as well as by numerical modeling. Measurements with CO2/CH4 and CO2/H2S flux ratios similar to mass ratios of sampled gases were considered as reflecting advective transport. A numerical model of CO2 migration in the subsoil system under fully water and gas saturated conditions was performed using the TOUGH2 code in order to reproduce semi-quantitatively field measurements. The main results show that high flux values produced by advective geothermal degassing can be very localized and that low and heterogeneous permeability conditions can induce low advective CO2 flux values. Therefore, in this case the populations discriminated by the GSA method should not be interpreted in terms of origin and/or transport mechanism but rather in terms of permeability conditions.

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

NASA Astrophysics Data System (ADS)

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

2014-05-01

The Acoculco caldera (Puebla, Mexico) has been identified by the Mexican Federal Electricity Company (in Spanish 'Comisión Federal de Electricidad', CFE) as a potential Enhanced Geothermal System (EGS) candidate. Two exploration wells were drilled and promising temperatures of ~300° C have been measured at a depth of 2000 m with a geothermal gradient of 11oC/100m, which is three times higher than the baseline gradient measured within the Trans-Mexican Volcanic Belt. As usually observed in Hot Dry Rock systems, thermal manifestations in surface are scarce and consist in low-temperature bubbling springs and soil degassing. The goals of this study were to identify the origin of these fluids, to estimate the soil degassing rate and to explore new areas for a future detailed exploration and drilling activities. Water and gas samples were collected for chemical and isotopic analysis (δ18O, δD, 3He/4He, 13C, 15N) and a multi-gas (CO2, CH4, H2S) soil survey was carried out using the accumulation chamber method. Springs' compositions indicate a meteoric origin and the dissolution of CO2 and H2S-rich gases, while gas compositions reveal a MORB-type origin mixed with some arc-type contribution. Gas geothermometry results are similar to temperatures measured during well drilling (260° C-300° C). Amongst all measured CO2 fluxes, only 5% (mean: 5543 g m-2 day-1) show typical geothermal values, while the remaining fluxes are low and correspond to biogenic degassing (mean: 18 g m-2 day-1). The low degassing rate of the geothermal system is a consequence of the intense hydrothermal alteration observed in the upper 800 m of the system which acts as an impermeable caprock. Highest measured CO2 fluxes (above > 600 g m-2 day-1) have corresponding CH4/CO2 flux ratios similar to mass ratios of sampled gases, which suggest an advective fluid transport. To represent field conditions, a numerical model was also applied to simulate the migration of CO2 towards the surface through a shallow aquifer under fully saturated conditions. By changing some of the aquifer properties (i.e., depth, permeability and porosity), it was found how geothermal CO2 fluxes can show values similar to a biogenic background flux. Future field work at Acoculco will include δ13C analysis together with soil flux measurements for a better discrimination of the degassing origin, and a thinner flux measurement grid will be defined for a better detection of any possible gas flux anomaly.

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

NASA Astrophysics Data System (ADS)

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

2013-05-01

Copahue volcano is part of the Caviahue-Copahue Volcanic Complex (CCVC), which is located in the southwestern sector of the Caviahue volcano-tectonic depression (Argentina-Chile). This depression is a pull-apart basin accommodating stresses between the southern Liquiñe-Ofqui strike slip and the northern Copahue-Antiñir compressive fault systems, in a back-arc setting with respect to the Southern Andean Volcanic Zone. In this study, we present chemical (inorganic and organic) and isotope compositions (δ13C-CO2, δ15N, 3He/4He, 40Ar/36Ar, δ13C-CH4, δD-CH4, and δD-H2O and δ18O-H2O) of fumaroles and bubbling gases of thermal springs located at the foot of Copahue volcano sampled in 2006, 2007 and 2012. Helium isotope ratios, the highest observed for a Southern American volcano (R/Ra up to 7.94), indicate a non-classic arc-like setting, but rather an extensional regime subdued to asthenospheric thinning. δ13C-CO2 values (from - 8.8‰ to - 6.8‰ vs. V-PDB), δ15N values (+ 5.3‰ to + 5.5‰ vs. Air) and CO2/3He ratios (from 1.4 to 8.8 × 109) suggest that the magmatic source is significantly affected by contamination of subducted sediments. Gases discharged from the northern sector of the CCVC show contribution of 3He-poor fluids likely permeating through local fault systems. Despite the clear mantle isotope signature in the CCVC gases, the acidic gas species have suffered scrubbing processes by a hydrothermal system mainly recharged by meteoric water. Gas geothermometry in the H2O-CO2-CH4-CO-H2 system suggests that CO and H2 re-equilibrate in a separated vapor phase at 200°-220 °C. On the contrary, rock-fluid interactions controlling CO2, CH4 production from Sabatier reaction and C3H8 dehydrogenation seem to occur within the hydrothermal reservoir at temperatures ranging from 250° to 300 °C. Fumarole gases sampled in 2006-2007 show relatively low N2/He and N2/Ar ratios and high R/Ra values with respect to those measured in 2012. Such compositional and isotope variations were likely related to injection of mafic magma that likely triggered the 2000 eruption. Therefore, changes affecting the magmatic system had a delayed effect on the chemistry of the CCVC gases due to the presence of the hydrothermal reservoir. However, geochemical monitoring activities mainly focused on the behavior of inert gas compounds (N2 and He), should be increased to investigate the mechanism at the origin of the unrest started in 2011.

Development of olivine crystallographic preferred orientation in response to strain-induced fabric geometry

NASA Astrophysics Data System (ADS)

Chatzaras, Vasileios; Kruckenberg, Seth C.; Cohen, Shaina M.; Medaris, L. Gordon, Jr.; Withers, Anthony C.; Bagley, Brian

2016-04-01

The effect of finite strain ellipsoid geometry on crystallographic preferred orientation (CPO) is well known for crustal minerals (e.g., quartz, calcite, biotite, and hornblende). In the upper mantle, however, it remains poorly constrained how strain and fabric may affect olivine CPO. We present data from a suite of 40 spinel peridotite xenoliths from Marie Byrd Land (west Antarctica), which support an interpretation that fabric geometry rather than deformation conditions control the development of olivine CPO. We use X-ray computed tomography (XRCT) to quantitatively determine spinel fabric (orientation and geometry). Olivine CPOs, determined by Electron Backscattered Diffraction (EBSD), are plotted with respect to the XRCT-derived spinel foliation and lineation; this approach allows for the accurate, and unbiased, identification of CPO symmetries and types in mantle xenoliths. The combined XRCT and EBSD data show that the xenoliths are characterized by a range of fabric geometries (from oblate to prolate) and olivine CPO patterns; we recognize the A-type, axial-[010], axial-[100], and B-type patterns. The mantle xenoliths equilibrated at temperatures 779-1198 oC, as determined by 2-Px geothermometry. Using a geotherm consistent with the stability of spinel in all xenoliths, the range of equilibration temperatures occurs at depths between 39 and 72 km. Olivine recrystallized grain size piezometry reveals differential stresses ranging 2-60 MPa. Analysis of low-angle misorientation axes show a wide range in the distribution of rotation axes, with dominant {0kl}[100] slip. We use Fourier Transform Infrared (FTIR) spectroscopy to estimate the water content in the xenolith with the B-type CPO pattern. FTIR analysis shows that the equilibrium H concentration in olivine is low (4-13 ppm H2O). Combining these data, we observe that olivine CPO symmetry is controlled neither by the deformation conditions (stress, temperature, pressure, water content) for the range of conditions estimated in the Marie Byrd Land xenoliths, nor by the activation of the slip systems predicted by deformation experiments. Rather, our data show that olivine CPO is controlled by transitions in strain-induced fabric geometry. Microstructures and deformation mechanism maps suggest that deformation is dominated by dislocation-accommodated grain boundary sliding. We propose that slip of olivine glide planes and rotation of olivine grains occur so as to accommodate the imposed material flow, which is guided by the 3D strain-induced fabric geometry. As a result of this process, the axial-[010] and B-type patterns form in relation to oblate fabric ellipsoids, the A-type pattern forms in a range of fabric ellipsoids, and the axial-[100] pattern is associated with prolate fabric ellipsoids. We therefore suggest that the well-known process of strain geometry-induced development of CPO is also applicable to upper mantle rocks.

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

USGS Publications Warehouse

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

2003-01-01

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

Caledonian evolution of the Moine Supergroup: Prograde garnet growth and context for quartz fabric-based deformation thermometry

NASA Astrophysics Data System (ADS)

Law, Richard; Ashley, Kyle; Thigpen, Ryan

2014-05-01

Despite the detailed Caledonian structural/tectonic framework developed for the Moine Supergroup of northern Scotland, debate continues over the tectonic processes that drove metamorphism. Rapid temporal evolution of the metamorphic sequence has led some geologists to suggest that crustal thickening alone cannot provide sufficient heat flow to reach the metamorphic grades observed. Rather, they postulate that large-scale contact metamorphism or initial heating in an extensional, back-arc setting is required. We present coupled petrographic analyses and forward phase stability modeling for quantifying prograde metamorphic evolution in pelite horizons dispersed across the Caledonian thrust sheets. Results suggest garnet growth was syn-kinematic during prograde decompression. Rutile and ilmenite inclusions in garnet cores and rims, respectively, support this claim, while chemical profiles and crystal morphology argue against a detrital origin for these garnet grains. The observed clockwise P-T path for these garnets is incompatible with extensional or contact metamorphic models (would require counter-clockwise paths). Rather, the P-T data suggests advection of isotherms during thrusting as the dominant mechanism for metamorphism (Thigpen et al., 2013). Recent studies in other orogens (e.g., Spear et al., 2012) suggest that heating over long time scales under mid-crustal conditions may not be needed to reach the metamorphic grades observed. Therefore the structurally higher, more hinterland Caledonian thrust sheets may have reached peak metamorphism in a much shorter time period than previously expected. The paucity of pelitic horizons across the foreland-positioned Moine thrust sheet has previously limited insight into the prograde evolution of these rocks. However, the dominance of quartz-rich units has allowed the thermal structure of the thrust sheet to be evaluated using quartz c-axis fabric opening angle-based deformation thermometry. Microstructures in the pelites sampled indicate that garnet (rim) growth is syn-kinematic with respect to the Scandian (mid-Silurian) deformation fabrics. Deformation temperatures indicated by quartz fabric opening angles are very similar to temperatures of metamorphism constrained using pseudosection and petrographic data from adjacent pelite horizons. This suggests that the deformation- and petrology-based data sets are providing information on the same thermal event. These results support the use of quartz deformation thermometry in obtaining thermal profiles across tectonic units where rock types (usually pelites), with metamorphic mineral assemblages suitable for petrology-based thermometry, are not present. Thigpen, J.R., Law, R.D., Loehn, C.L., Strachan, R.A., Tracy, R.J., Lloyd, G.E., Roth, B.L., and Brown, S.J., 2013, Thermal structure and tectonic evolution of the Scandian orogenic wedge, Scottish Caledonides: integrating geothermometry, deformation temperatures and conceptual kinematic-thermal models, J. Metamorphic Geol., 31, 813-842. Spear, F.S., Ashley, K.T., Webb, L.E., and Thomas, J.B., 2012, Ti diffusion in quartz inclusions: implications for metamorphic time scales, Contrib. Mineral Petrol., 164, 977-986.

STRUCTURAL CONTROLS OF THE EMERSON PASS GEOTHERMAL SYSTEM, NORTHWESTERN NEVADA: CHARACTERIZATION OF A "BLIND" SYSTEM

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

Anderson, Ryan B; Faulds, James E

The Pyramid Lake area is favorable for geothermal development due to the tectonic setting of the region. The Walker Lane belt, a dextral shear zone that accommodates ~20% relative motion between the Pacific and North American plates, terminates northwestward in northeast California. NW-directed dextral shear is transferred to WNW extension accommodated by N-to -NNE striking normal faults of the Basin and Range. As a consequence, enhanced dilation occurs on favorably oriented faults generating high geothermal potential in the northwestern Great Basin. The NW-striking right-lateral Pyramid Lake fault, a major structure of the northern Walker Lane, terminates at the southern endmore » of Pyramid Lake and transfers strain to the NNE-striking down to the west Lake Range fault, resulting in high geothermal potential. Known geothermal systems in the area have not been developed due to cultural considerations of the Pyramid Lake Paiute Tribe. Therefore, exploration has been focused on discovering blind geothermal systems elsewhere on the reservation by identifying structurally favorable settings and indicators of past geothermal activity. One promising area is the northeast end of Pyramid Lake, where a broad left step between the west-dipping range-bounding faults of the Lake and Fox Ranges has led to the formation of a broad, faulted relay ramp. Furthermore, tufa mounds, mineralized veins, and altered Miocene rocks occur proximal to a thermal anomaly discovered by a 2-m shallow temperature survey at the north end of the step-over in Emerson Pass. Detailed geologic mapping has revealed a system of mainly NNE-striking down to the west normal faults. However, there are three notable exceptions to this generality, including 1) a prominent NW-striking apparent right-lateral fault, 2) a NW-striking down to the south fault which juxtaposes the base of the mid-Miocene Pyramid sequence against younger late Tertiary sedimentary rocks, and 3) a NNE-striking down to the east normal fault, which accommodates motion such that the Mesozoic Nightingale sequence is juxtaposed with late Tertiary sedimentary rocks. The NW dextral fault, the NNE-down to east fault, and several NNE-down to the west faults intersect roughly at the thermal anomaly in Emerson Pass. This suggests that fault intersections locally control upwelling of geothermal fluids within the step-over. Based on this assumption, it is proposed that the area near Buckbrush Springs be investigated further for geothermal potential. At this location, a NNE-down to the west normal fault, with >1 km of offset, intersects a NW-striking down to the south fault at a small left step in the NNE fault. Further studies will include collection of available kinematic indicators near the shallow thermal anomaly in Emerson Pass, geothermometry on Buckbrush Spring, and possibly drilling of temperature gradient wells in Emerson Pass and at Buckbrush Spring.« less

A tale of two magmas: Petrological insights into mafic and intermediate Plinian volcanism at Volcán de Colima, Mexico

NASA Astrophysics Data System (ADS)

Crummy, J. M.; Savov, I. P.; Morgan, D. J.; Wilson, M.; Loughlin, S.; Navarro-Ochoa, C.

2012-12-01

Volcán de Colima in western Mexico explosively erupts basaltic to high-silica andesitic magmas. Detailed petrological and geochemical analyses of Holocene tephra fallout deposits reveal two distinct magma types: I. typical calc-alkaline series magmas; and II. mixed calc-alkaline - alkaline magmas. Group I magmas comprise basalt to high-silica andesite (50.7 to 60.4 wt.% SiO2) and typically contain phenocrysts of plagioclase + clinopyroxene + orthopyroxene + Fe-Ti oxides ± hornblende ± olivine. Crystallinity varies from 10-25 vol.% dominated by plagioclase in a groundmass comprising highly vesiculated glass with abundant microlites. Back-scatter electron (BSE) microscope images together with electron microprobe analyses (EPMA) reveal complex zoning patterns and compositional variations in plagioclase and pyroxene phenocrysts. Large scale resorption events with dissolution surfaces cross-cutting multiple growth zones, combined with large steps in An content of up to 20 mol.% in plagioclase, and Mg# varying from 0.74 to 0.86 in clinopyroxene and orthopyroxene, indicates destabilisation and recrystallisation in a more mafic melt: increases in Cr coincident with step increases in Mg# reveal mafic magma recharge. Many plagioclase and pyroxene phenocrysts record multiple magma recharge events; while small-scale oscillations reveal compositional fluctuations as a result of decompression and degassing. Group II magmas comprise basalt to basaltic-andesite (48.3 to 57.5 wt.% SiO2) and contain 10-15 vol.% crystals comprising clinopyroxene + olivine + phlogopite + plagioclase + Fe-Ti oxides ± hornblende ± orthopyroxene. The groundmass comprises highly vesiculated glass with abundant microlites of the same mineral phases. Clinopyroxene phenocrysts have magnesian cores (Mg# 0.88-0.89) that display strong dissolution with clear resorption and recrystallisation. EPMA analyses reveal large compositional differences with the surrounding growth zone (Mg# 0.80) indicating recrystallisation and re-equilibration within a compositionally different melt. This composition of the clinopyroxene is similar to that of the Group I magmas. Whole-rock geochemical and Sr and Nd isotopic analyses reveal strong trends in the Group II magmas towards the composition of monogenetic cinder cones composed of phlogopite-bearing alkaline lamprophyre situated to the north of Volcán de Colima. The alkaline magmas are thought to have formed from partial melting of metasomatically enriched veins within the lithospheric mantle. We suggest the high Mg clinopyroxene cores of the Group II magmas crystallised from such alkaline melts, which then mixed with the parental mantle-derived melts of the Group I magmas. Geothermometry and hygrometry based on mineral-mineral and mineral-melt equilibria reveal no correlation between variations in eruption temperature (930-1000°C) and magmatic H2O content (3-6 wt.%) with magma composition. This implies magma composition and volatile content are not controlling the highly explosive mafic and intermediate eruptions at Volcán de Colima, but rather, are driven by very fast ascent rates from source to surface.

Petrology, geochemistry and zircon U-Pb geochronology of a layered igneous complex from Akarui Point in the Lützow-Holm Complex, East Antarctica: Implications for Antarctica-Sri Lanka correlation

NASA Astrophysics Data System (ADS)

Kazami, Sou; Tsunogae, Toshiaki; Santosh, M.; Tsutsumi, Yukiyasu; Takamura, Yusuke

2016-11-01

The Lützow-Holm Complex (LHC) of East Antarctica forms part of a complex subduction-collision orogen related to the amalgamation of the Neoproterozoic supercontinent Gondwana. Here we report new petrological, geochemical, and geochronological data from a metamorphosed and disrupted layered igneous complex from Akarui Point in the LHC which provide new insights into the evolution of the complex. The complex is composed of mafic orthogneiss (edenite/pargasite + plagioclase ± clinopyroxene ± orthopyroxene ± spinel ± sapphirine ± K-feldspar), meta-ultramafic rock (pargasite + olivine + spinel + orthopyroxene), and felsic orthogneiss (plagioclase + quartz + pargasite + biotite ± garnet). The rocks show obvious compositional layering reflecting the chemical variation possibly through magmatic differentiation. The metamorphic conditions of the rocks were estimated using hornblende-plagioclase geothermometry which yielded temperatures of 720-840 °C. The geochemical data of the orthogneisses indicate fractional crystallization possibly related to differentiation within a magma chamber. Most of the mafic-ultramafic samples show enrichment of LILE, negative Nb, Ta, P and Ti anomalies, and constant HFSE contents in primitive-mantle normalized trace element plots suggesting volcanic arc affinity probably related to subduction. The enrichment of LREE and flat HREE patterns in chondrite-normalized REE plot, with the Nb-Zr-Y, Y-La-Nb, and Th/Yb-Nb/Yb plots also suggest volcanic arc affinity. The felsic orthogneiss plotted on Nb/Zr-Zr diagram (low Nb/Zr ratio) and spider diagrams (enrichment of LILE, negative Nb, Ta, P and Ti anomalies) also show magmatic arc origin. The morphology, internal structure, and high Th/U ratio of zircon grains in felsic orthogneiss are consistent with magmatic origin for most of these grains. Zircon U-Pb analyses suggest Early Neoproterozoic (847.4 ± 8.0 Ma) magmatism and protolith formation. Some older grains (1026-882 Ma) are regarded as xenocrysts from basement entrained in the magma through limited crustal reworking. The younger ages (807-667 Ma) might represent subsequent thermal events. The results of this study suggest that the ca. 850 Ma layered igneous complex in Akarui Point was derived from a magma chamber constructed through arc-related magmatism which included components from ca. 1.0 Ga felsic continental crustal basement. The geochemical characteristics and the timing of protolith emplacement from this complex are broadly identical to those of similar orthogneisses from Kasumi Rock and Tama Point in the LHC and the Kadugannawa Complex in Sri Lanka, which record Early Neoproterozoic (ca. 1.0 Ga) arc magmatism. Although the magmatic event in Akarui Point is slightly younger, the thermal event probably continued from ca. 1.0 Ga to ca. 850 Ma or even to ca. 670 Ma. We therefore correlate the Akarui Point igneous complex with those in the LHC and Kadugannawa Complex formed under similar Early Neoproterozoic arc magmatic events during the convergent margin processes prior to the assembly of the Gondwana supercontinent.

Re-examining Distal Facies of the Grand Bay Ignimbrite at Fond St. Jean, Dominica

NASA Astrophysics Data System (ADS)

Ebner, N.; Frey, H. M.; Wirth, K. R.; Waters, L. E.; Manon, M. R. F.

2017-12-01

The Grand Bay ignimbrite in southern Dominica is a relatively young (43 ± 13 ka by U-Th of zircon), voluminous (0-.5-1 km3 on-land) and laterally extensive pyroclastic flow deposit spanning over 20 km2 that has been associated with the Micotrin volcanic center or Plat Pays complex. The Grand Bay ignimbrite typically occurs as a massive valley fill facies, approximately 9-14 meters thick, exposed on the southern coastal road, rich in white-light gray, relatively crystal rich (25-31%) andesitic (62-63.5 wt% SiO2, 16.7 wt% Al2O3, 6.5 wt % Fe2O3) pumice, whose mineral assemblage is dominated by plagioclase (22-25%), orthopyroxene (3-4%), and clinopyroxene (1-1.5%), in an unconsolidated gray ashy matrix. In the literature, distal facies of the Grand Bay ignimbrite have been proposed at Fond St. Jean (FSJ), but this supposition has recently been called into question. The 9 m thick stratified Fond St. Jean ignimbrite, (38,890 k.a. ± 600 B.P. by14C), is weathered yellow orange and overlies a 4 m thick lithified beach deposit on a sharp contact. Andesitic pumice clasts (60.5-64.5 wt% SiO2, 18 wt% Al2O3, 5.5 wt % Fe2O3) from the base of the FSJ ignimbrite contain similar mineral assemblages to Grand Bay clasts, however, FSJ pumices are relatively less crystal-rich (16-19%), contain significantly less plagioclase (13-16%), opx (1.0-1.5%), cpx (0.1 - 0.6%), and, most strikingly, up to 1% hornblende, which was not present in any Grand Bay samples. The lowermost three meters of the FSJ ignimbrite sequence is composed of meter thick sections of clast (5-7 cm pumice and ≤1 cm lithics) supported beds (70 cm), grading upwards into 30 cm of ash laminations and small pumice clasts (1-3 cm). Following a 40 cm bed of massive ash containing 1-3 cm clasts of pumice, the initial sequence repeats itself for 5 meters, with 30-40 cm lithic blocks in the uppermost unit. In addition to the stark stratigraphic and petrographic differences from the Grand Bay Beach exposure, Fe-Ti oxide geothermometry reveals eruption temperature of 820 + 7°C at Grand Bay Beach (ΔNNO - 0.16) and 864 ± 33 °C (ΔNNO - 0.25) at Fond St. Jean. Plagioclase composition ranges from An51-88 at Grand Bay and An57-75 at Fond St. Jean respectively. Furthermore, plagioclase hygrometry shows a range of 7.8 to 7.3 wt% H2O at Grand Bay, with slightly drier conditions of 7.3 to 7.1 wt% H2O at Fond St. Jean.

Geochemistry of tectonically expelled fluids from the northern Coast ranges, Rumsey Hills, California, USA

USGS Publications Warehouse

Davisson, M.L.; Presser, T.S.; Criss, R.E.

1994-01-01

Tectonic compression has created abnormally high pressure on deep basinal fluids causing their expulsion from areally exposed Upper Cretaceous rock along the eastern margin of the California Coast ranges. The fluids emerge as near-neutral, perennial sodium chloride springs at high elevations with flow rates as high as 10 L per min. Higher spring discharges are more common around the exposure of a west-vergent fault propagation fold axis. Spring waters range from ~1000 to 27,000 mg/L TDS. The least saline water (??18O = -7.5???) closely represents local meteoric water that mixes with saline fluid (??18O = +5.3???) and forms a slope of ~3.5 on a ??D vs. ??18O plot. A Na (125 to 8000 mg/L) vs. Cl (150 to 17,000 mg/L) plot shows a linear dilution trend that extends close to, but below, the values for modern seawater. Calcium (75-3000 mg/L) is considerably enriched relative to seawater and forms a nonlinear trend with chloride. In detail, the "Na deficit," defined by the difference between the measured Na content and the Na concentration on a hypothetical seawater dilution line, is approximately balanced by the Ca excess, similarly defined by the seawater dilution line. This relationship strongly suggests that the fluid is diluted seawater that is being modified by active albitization of plagioclase at different depths. Simultaneous B and 18O enrichment of the fluids, accompanied by deuterium depletion, further suggest that the seawater modification is influenced by clay diagenesis. Bicarbonate and SiO2 concentrations show an inverse correlation with Cl, with most waters being saturated or slightly oversaturated with calcite and quartz at the discharge temperatures. Some freshwater springs with near-meteoric stable isotope values may represent mixing of young groundwater from perched aquifers, but in many cases, the freshwater springs emerge along the same structures and have the same perennial nature as the saline fluids, and expulsion of an older fresh groundwater component that is under abnormal fluid pressures cannot be ruled out. Basinal fluids elsewhere commonly show dilution trends with local meteoric water, and in the case of the Rumsey Hills, some of the dilute saline waters may indicate deep penetration of meteoric water (> 1 km) in the Pleistocene before the latest tectonic uplift. Geothermometry of the spring waters (maximum ~90??C) suggest an origin from as deep as 4.0 km. This depth is consistent with the depth of the core of a fault propagation anticline below the surface of the Rumsey Hills developed by active internal deformation of an east-tapering wedge beneath the southwestern Sacramento Valley. Active tectonic compression causes near-lithostatic fluid pressures in the shallow subsurface below the Rumsey Hills and volume strain within the core of the anticline that results in upward expulsion of the saline fluids from the indicated depths. ?? 1994.

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

NASA Astrophysics Data System (ADS)

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

2018-01-01

The Gölemezli Geothermal Field (GGF) is one of the best known geothermal fields in western Anatolia (Turkey). The exploited fluids are of meteoric origin, mixed with deep magmatic fluids, which interacted with the metamorphic rocks of the Menderes Massif. The geothermal fluids are channeled along Quaternary faults belonging to the main normal faults system delimiting the northern side of the Denizli Basin and their associated transfer zones. In this study, hydrochemical and isotopic analyses of the thermal and cold waters allow us to determine water-rock interactions, fluid paths and mixing processes. Two groups of thermal waters have been distinguished: (i) Group 1A, comprising Na-SO4 type and Ca-SO4 type and (ii) Group 1B, only consisting Ca-HCO3 type waters. Differently, two groups were recognized in the cold waters: (i) Group 2A, corresponding to Ca-HCO3 type and (ii) Group 2B, including Mg-HCO3 type. Their geochemical characteristics indicate interactions with the Paleozoic metamorphic rocks of the Menderes Massif and with the Neogene lacustrine sedimentary rocks. Dissolution of host rock and ion-exchange reactions modify thermal water composition in the reservoir of the GGF. High correlation in some ionic ratios and high concentrations of some minor elements suggest an enhanced water-rock interaction. None of the thermal waters has been reached a complete chemical re-equilibrium, possibly as a result of mixing with cold water during their pathways. Geothermal reservoir temperatures are calculated in the range of 130-210°C for the Gölemezli field. Very negative δ18O and δ2H isotopic ratios are respectively between -8.37 and -8.13‰ and -61.09 and -59.34‰ for the SO4-rich thermal waters, and ca. - 8.40 and -8.32‰ and - 57.80 and -57.41‰ for the HCO3-rich thermal waters. Low tritium (< 1 TU) and low oxygen isotope values reflect a deep circuit and fluids of meteoric origin. Positive δ13CDIC ratios (+ 5.11 to + 7.54‰) of all thermal waters imply a contribution of metamorphic origin. Heating is guaranteed by a deep circuit within an overheated continental crust, mainly affected by damaged rock volumes. Volatile ascent from deep magmatic sources through crustal structures can explain the occurrence of mantle volatiles at shallow depth in the Denizli Basin. The NW- and NE-trending fault systems, associated with their related fractures, played as hydraulic conduits underlining the strict link existing between fractures and fluid convection in the extensional settings. In this view, the GGF is a very good example of geothermal field associated to active tectonic setting and magmatism, as it is the case of the other geothermal fields occurring in the Denizli Basin.

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

NASA Astrophysics Data System (ADS)

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

2018-06-01

The Meishan iron deposit contains 338 Mt of iron-ore reserves at 39% Fe and represents the largest magnetite-apatite deposit in the Ningwu Basin of eastern China. Controversy has long existed about whether this deposit had a hydrothermal or iron-oxide melt origin. Iron mineralization is genetically related to plutons that are composed of gabbro-diorite, which were emplaced at 130 ± 1 Ma. These rocks have SiO2 contents of 51.72-54.60 wt%, Na2O contents of 3.47-4.04 wt%, K2O contents of 2.02-2.69 wt%, and K2O/Na2O ratios of 0.51-0.73. These rocks are enriched in LILEs and LREEs and depleted in Nb, Ta, and Ti, which indicates that the magma originated through partial melting of an enriched lithospheric mantle source in a subduction environment. A pattern of decreasing initial Sr isotopic ratios and increasing εNd(t) values with time in Early Cretaceous magmatic rocks of the Ningwu Basin may indicate incorporation of increasing proportions of asthenospheric mantle material into the source magma, which is consistent with the processes of lithospheric thinning and asthenospheric upwelling in eastern China related to Mesozoic subduction of the Paleo-Pacific Plate. Two stages of magnetite are found in the gabbro-diorite: (1) early-crystallized magnetite as euhedral-subhedral crystals in larger clinopyroxene crystals, and (2) later-crystallized magnetite and accompanying ilmenite grains in the voids between plagioclase and clinopyroxene crystals. The formation of magnetite before clinopyroxene, combined with the results of Fe-Ti oxide geothermometry and analysis of magnetite V content, indicates that the oxygen fugacity of the source magma was greater than ΔFMQ +2.2 at an early stage (>640 °C) but decreased to ΔFMQ -2.66 as abundant magnetite crystallized at a later stage (∼489 °C). The early crystallization of magnetite at a high oxygen fugacity does not support a Fenner evolution trend for the primitive magma and diminishes the likelihood of liquid immiscibility, which could have generated an iron-rich melt, and is thus inconsistent with an iron-oxide melt origin for the Meishan iron deposit. The δ34S values of pyrite (6.6-15.1‰) and anhydrite (15.6-16.9‰) in the deposit and the occurrence of evaporites under the volcanic rocks likely indicate that the iron ores and alteration rocks of the Meishan deposit were formed by the circulation of fluids of evaporitic origin driven by heat from the hypabyssal gabbro-diorite intrusives. In the late magmatic stage, oxygen fugacity decreased to a reducing range, triggering the reduction of sulfate to reduced sulfur and leading to local gold and pyrite mineralization.

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

USGS Publications Warehouse

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

2013-01-01

The Iceland Deep Drilling Project Well 1 was designed as a 4- to 5-km-deep exploration well with the goal of intercepting supercritical hydrothermal fluids in the Krafla geothermal field, Iceland. The well unexpectedly drilled into a high-silica (76.5 % SiO2) rhyolite melt at approximately 2.1 km. Some of the melt vesiculated while extruding into the drill hole, but most of the recovered cuttings are quenched sparsely phyric, vesicle-poor glass. The phenocryst assemblage is comprised of titanomagnetite, plagioclase, augite, and pigeonite. Compositional zoning in plagioclase and exsolution lamellae in augite and pigeonite record changing crystallization conditions as the melt migrated to its present depth of emplacement. The in situ temperature of the melt is estimated to be between 850 and 920 °C based on two-pyroxene geothermometry and modeling of the crystallization sequence. Volatile content of the glass indicated partial degassing at an in situ pressure that is above hydrostatic (~16 MPa) and below lithostatic (~55 MPa). The major element and minor element composition of the melt are consistent with an origin by partial melting of hydrothermally altered basaltic crust at depth, similar to rhyolite erupted within the Krafla Caldera. Chondrite-normalized REE concentrations show strong light REE enrichment and relative flat patterns with negative Eu anomaly. Strontium isotope values (0.70328) are consistent with mantle-derived melt, but oxygen and hydrogen isotope values are depleted (3.1 and −118 ‰, respectively) relative to mantle values. The hydrogen isotope values overlap those of hydrothermal epidote from rocks altered by the meteoric-water-recharged Krafla geothermal system. The rhyolite melt was emplaced into and has reacted with a felsic intrusive suite that has nearly identical composition. The felsite is composed of quartz, alkali feldspar, plagioclase, titanomagnetite, and augite. Emplacement of the rhyolite magma has resulted in partial melting of the felsite, accompanied locally by partial assimilation. The interstitial melt in the felsite has similar normalized SiO2 content as the rhyolite melt but is distinguished by higher K2O and lower CaO and plots near the minimum melt composition in the granite system. Augite in the partially melted felsite has re-equilibrated to more calcic metamorphic compositions. Rare quenched glass fragments containing glomeroporphyritic crystals derived from the felsite show textural evidence for resorption of alkali feldspar and quartz. The glass in these fragments is enriched in SiO2 relative to the rhyolite melt or the interstitial felsite melt, consistent with the textural evidence for quartz dissolution. The quenching of these melts by drilling fluids at in situ conditions preserves details of the melt–wall rock interaction that would not be readily observed in rocks that had completely crystallized. However, these processes may be recognizable by a combination of textural analysis and in situ analytical techniques that document compositional heterogeneity due to partial melting and local assimilation.

Geochemistry, thermometry and isotope ratios on the same zircon crystals: the tandem use of quadrupole LA-ICPMS and CA-TIMS

NASA Astrophysics Data System (ADS)

Olin, P. H.; Schmitz, M. D.; Crowley, J. L.

2011-12-01

Current trends in igneous petrology include the extraction of diverse geochemical information from smaller sample targets by ever more efficient and cost effective means. Igneous zircons are repositories of several types of petrogenetic information, such as magmatic crystallization ages obtained using U-Pb geochronology, magmatic temperatures using Ti-in-zircon geothermometry, and magmatic differentiation and/or mixing trends using trace element contents. Here we demonstrate a tandem quadrupole LA-ICPMS and CA-TIMS approach on single zircon crystals and within domains in single crystals, which extracts all of these data from a single laser spot analysis and then guides the acquisition of CA-TIMS ages at precisions relevant to magmatic histories. We present data from zircon-bearing intrusive and extrusive rocks spanning the compositional spectrum, and highlight results from silicic volcanic rocks with different affinities. The utility of our approach is illustrated in zircons from the Temora diorite, a commonly used standard material which we analysed using 25-μm ablation spots placed on dozens of grains which had been previously annealed and chemically abraded prior to mounting in epoxy. Our LA-ICPMS results illustrate a 3- to 5-fold variation in trace element concentrations and trace element ratios over >150 degrees of cooling as estimated from Ti-in-zircon thermometry. Some geochemical parameters (e.g., Nb/Ta variations and Eu anomalies) are consistent with crystal fractionation during progressive crystallization, while others are bimodal (e.g., Hf and U contents), suggesting the mixing of crystal/magma batches prior to final solidification. LA-ICPMS U-Pb spot ages reproduce the accepted CA-TIMS age within 2% precision and accuracy, while our CA-TIMS results on the same grains constrain the development of the observed geochemical variability to within 100 ka. Other zircon standard materials to be presented include Plesovich syenite, FC1 gabbro, and R33 diorite. Analyses of zircons from selected western Snake River Plain silicic volcanic units further demonstrate the capability of our approach. These units are targeted with the overarching goal of better understanding magmatism in the region and to identify geochemical fingerprints to better distinguish among and to correlate between units. Several rhyolites distributed along the northern margin of the plain have LA-ICPMS ages of ca. 11 Ma, within error of each other and their CA-TIMS ages, and reveal differences in temperatures of crystallization and trace element contents and ratios. Individual units have crystallization temperatures that span 100 degrees or more, and show correlations with whole-rock major and trace element contents and ratios. In many cases, zircon geochemical parameters such as REE and Y contents, and Nb/Ta and Th/U ratios allow units proximal to each other to be distinguished from one another while also providing fingerprints to correlate to distal units on the south side of the plain or elsewhere in the province.

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.

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

NASA Astrophysics Data System (ADS)

Masoumi, Roohangiz

2017-04-01

Geological considerations in the east of Sabalan volcano indicate that the calc-alkaline volcanic-sedimentary units constitute the great volume of the geothermal reservoir in the study district. The rocks suffered argillic alteration acted as cap rocks for this reservoir. In some localities in the study district siliceous (chalcedony and opal) sinters were developed around the orifice of the hot springs. The geothermal fluids in the study district, in terms of physico-chemical parameters, have characteristics which differ from other geothermal fields around the Mount Sabalan particularly in the southern and northwestern districts. These differences are: (a) the measured pH values of the geothermal fluids range from approximately 4.5 to 8.8 signifying a variation from acidity to alkalinity; (b) the measured TDS values of these waters, in comparison with the average TDS values for most types of geothermal systems, are low and the minimum values were recorded in the Viladara area; (c) estimation of concentration values of anions and cations in the selected spring water samples indicate that they have chiefly chloride and bicarbonate anions however, samples from the Sardabeh area contain relatively high sulfate (SO42-) content. The concentration values of rare elements in these waters are noticeable. Selenium has the highest concentration value (170 mg/l) among the rare elements. The maximum concentration values of boron and arsenic were measured to be 7 mg/l and 10 mg/l, respectively. The rest of rare elements have relatively low concentration values in the studied samples. The calculation of solute-based geothermometry was done on the basis of Na-Li, Na-K, Na-K, Ca, and silica for the water samples. The results of all these procedures for estimation of temperature of the geothermal reservoir in the east of Mount Sabalan were relatively very close to one another. Nevertheless, the temperatures determined by the Na-Li and Na-K geothermometric methods are 225°C and 239°C, respectively while by Na-K-Ca and silica methods are 181°C and 136°C, respectively for the geothermal reservoir. Consideration of hydrogen and oxygen stable isotopes (δ18O and δD) of the geothermal fluids in the east of Mount Sabalan revealed that their δD and δ18O values vary from -63.37‰ to -80.19‰ and from -9.96‰ to -13.4‰, respectively. The bivariate plot of δ18O versus δD shows that the data points mainly lie between lines GMWL and NMWL indicating that the great portion of these waters have meteoric origin and the role of magmatic waters is almost negligible. Consideration of unstable isotope of 3H delineated that the average 3H content of these waters is 5.1 TU. Illustration of diagrams of tritium-δ18O and tritium-Cl- showed that most of these waters are categorized as "sub-modern" waters and in respect of depth having shallow circulation. Key words: Sabalan volcano, geology, hydrogeochemistry, stable isotopes, NW Iran.

Oxygen Isotope and Microtextural Evidence for Fluctuations in Fluid Pressure During Contact Metamorphism, Alta Aureole, Utah, USA

NASA Astrophysics Data System (ADS)

Bowman, J. R.; Valley, J. W.; Kita, N.

2006-12-01

Thin section-scale textures record a detailed history of prograde and retrograde reactions in the periclase (Per) zone of the Alta Stock aureole. New ion microprobe (SIMS) measurements (10 micron spot, ±0.2 permil, 1sd) of the oxygen isotope compositions of the carbonates preserving these textures provide evidence for at least two cycles of oscillation of fluid pressure (Pfl) between lithostatic (PL) and hydrostatic (Phyd) conditions during evolution of the inner aureole. Infiltration of water-rich fluids during prograde metamorphism converted dolomite (Dol) to Per + calcite (Cal) marble and caused significant 18O/16O depletion in the Dol protolith (Initial δ18O (Cal) > +25 permil), producing Cal with δ18O values of +11 permil. The SIMS values approximate oxygen isotope exchange equilibrium with the Alta stock, indicating that infiltrating fluids were likely magmatic. Exsolution of fluid from the crystallizing magma, coupled with geothermometry from the periclase zone marbles, requires Pfl> PL. Horizontally-oriented expansion cracks filled with brucite (Br) extend from Br pseudomorphs after periclase, and cut retrograde Dol that partially to completely rims the Br pseudomorphs. This earlier retrograde Dol is significantly depleted in 18O/16O relative to matrix Cal, with δ18O of +5 to +7.1 permil. These lower δ18O values indicate that meteoric water infiltrated into the Per marbles during cooling and resulting partial back reaction of Per + Cal to Dol, prior to the hydration of the remaining Per to Br. Influx of meteoric water requires sufficient increase in permeability to permit surface- derived meteoric water to penetrate to the estimated 4.5 km depth of this structural level of the Alta aureole, and suggests a resulting decrease in Pfl to hydrostatic pressure conditions. The horizontally-oriented expansion cracks associated with the Br pseudomorphs indicate that sub-vertical expansion accompanied hydration of Per to Br, requiring that Pfl increase again to values equal to and even slightly in excess of PL. Subsequent formation of a second generation of sub-vertical Dol veins with very low δ18O values (-1.9 to +1.2 permil) indicates another stage of infiltration involving even greater amounts of meteoric water, and a return to hydrostatic Pflconditions. Hence the detailed microtextures in the Per zone marbles, and their δ18O values, measureable with the spatial resolution capability of the ion microprobe, record a history of fluctuating fluid pressure between lithostatic and hydrostatic conditions in the inner Alta aureole. Such fluctuations should not be surprising. Contact metamorphic environments are characterized by strong spatial and temporal gradients in temperature, and a number of thermally-dependent factors (e.g., compaction, crystallization, reaction-generated porosity, thermally-controlled expansion and contraction) would then interact dynamically as sealing and cracking mechanisms to both increase and decrease permeability. Further, transient increases in fluid pressure would be expected from production of volatiles by metamorphic reactions and from multiple pulses of magmatic fluid produced during the assembly of an igneous intrusion.

Geochemical constraints on the genesis of the Scheelite dome intrusion-related gold deposit, Tombstone gold belt, Yukon, Canada

USGS Publications Warehouse

Mair, J.L.; Goldfarb, R.J.; Johnson, C.A.; Hart, C.J.R.; Marsh, E.E.

2006-01-01

The Scheelite dome intrusion-related gold deposit, western Selwyn basin, Yukon, is hosted in hornfelsed metasedimentary strata that lie adjacent to the exposed apices of a monzogranite to quartz monzonite plutonic complex of the mid-Cretaceous Tombstone-Tungsten magmatic belt, Tintina gold province, Alaska and Yukon. A variety of mineralization styles occur throughout a 10- ?? 3-km east-trending corridor and include reduced Au- and W-rich skarns, Au, W- and Ag-Pb-Zn-Sb-rich quartz tension-vein arrays, and multiphase fault veins and isolated zones of Au-rich sericite-carbonate altered rock. Integrated U-Pb SHRIMP data for magmatic zircon and Ar-Ar data for magmatic and hydrotbermal biotite indicate that gold mineralization occurred within 1 to 2 m.y. of magma emplacement. Fluid inclusion, oxygen isotope, and arsenopyrite geothermometry data indicate that hydrothermal minerals formed at depths of 6 to 9 km over a temperature range from 550??C. High-temperature Au-rich skarns formed at >400??C, whereas vein-hosted mineralization formed at 280?? to 380??C. In skarns, Au is strongly associated with enrichments of Bi, Te, W, and As, whereas a variety of Au-rich veins occur, with Asrich (type 1), and Te- and W-rich (type 2) end members. Silver-Pb-Zn-Sb veins are typically Au poor and represent the latest and lowest temperature phase in the hydrothermal paragenesis. The fluid inclusion data indicate that all mineralization styles were formed from low-salinity (???4 wt % NaCl equiv) aqueous-carbonic fluids, consistent with the composition of fluid inclusions within infilled miarolitic cavities in the intrusive rocks. However, the nonaqueous fluid was predominantly CH4 in skarn, CO2 in Au-Te and Au-W veins, and a fluid with roughly equal amounts Of CO2, CH4, and N2 in Au-As and Ag-Pb-Zn-Sb veins. Oxygen isotope data are consistent with a mineralizing fluid of predominantly magmatic origin that was variably modified to more positive ??18O values during interaction with 18O-enriched metasedimentary strata. Sulfur isotope data suggest two possible sources of sulfur, a magmatic source characterized by ??34S values of approximately -5 to 0 per mil and sulfur from the metasedimentary country rocks characterized by more negative ??34S values of approximately -15 to -10 per mil. Collectively the data indicate that gold at Scheelite Dome was deposited from a magmatic-hydrothermal system. Interaction of magmatic fluids with graphitic hornfels rocks resulted in reduction of the ore fluids, higher CH4/CO2 ratios, and modification of the oxygen and sulfur isotope values of the ore fluids toward those of the metasedimentary hornfels. Progressive reduction and cooling of hydrotbermal fluids, in addition to phase separation in vein-hosted mineralization, were the mechanisms for gold deposition. Compared to other intrusion-related gold deposits associated with the Tombstone-Tungsten magmatic belt magmatism, exposed mineralization at Scheelite Dome is predominantly hosted by hornfelsed metasedimentary rocks. This results in more diverse mineralization styles and a greater spread of isotope and fluid inclusion data. ?? 2006 Society of Economic Geologists, Inc.

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.

Integrated Field Analyses of Thermal Springs

NASA Astrophysics Data System (ADS)

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

2011-12-01

A group of undergraduate researchers through the SURE internship offered by the Southern California Earthquake Center (SCEC) have examined thermal springs in southern Idaho, northern Utah as well as mud volcanoes in the Salton Sea, California. We used an integrated approach to estimate the setting and maximum temperature, including water chemistry, Ipad-based image and data-base management, microbiology, and gas analyses with a modified Giggenbach sampler.All springs were characterized using GISRoam (tmCogent3D). We are performing geothermometry calculations as well as comparisons with temperature gradient data on the results while also analyzing biological samples. Analyses include water temperature, pH, electrical conductivity, and TDS measured in the field. Each sample is sealed and chilled and delivered to a water lab within 12 hours.Temperatures are continuously monitored with the use of Solinst Levelogger Juniors. Through partnership with a local community college geology club, we receive results on a monthly basis and are able to process initial data earlier in order to evaluate data over a longer time span. The springs and mudpots contained microbial organisms which were analyzed using methods of single colony isolation, polymerase chain reaction, and DNA sequencing showing the impact of the organisms on the springs or vice versa. Soon we we will collect gas samples at sites that show signs of gas. This will be taken using a hybrid of the Giggenbach method and our own methods. Drawing gas samples has proven a challenge, however we devised a method to draw out gas samples utilizing the Giggenbach flask, transferring samples to glass blood sample tubes, replacing NaOH in the Giggenbach flask, and evacuating it in the field for multiple samples using a vacuum pump. We also use a floating platform devised to carry and lower a levelogger, to using an in-line fuel filter from a tractor in order to keep mud from contaminating the equipment.The use of raster imagery on the iPad2 has drastically changed how we plan and conduct our sampling trips. Orthoimagery onto the iPad2 is viewed with GISRoam and we use that imagery to help guide us toward points that we wish to visit. GISRoam was used to plot spatially correlated data points while in the field, estimate latitude and longitude, and record aforementioned data. A key factor to our success is up to the minute collaboration between all participants. Google's suite of services provides phone number for landowners, web site hosting, and the most crucial implementation for sharing data in real time has been the beta google Fusion Table. This spreadsheet allows for the incorporation of images, sample data and GPS location to be displayed as a kml file to be viewed in Google maps. This ability to modify and recognize data points in real time has made us more effective in the field, and in documenting progress in the lab. This workflow has enabled us to sample over 30 springs in 2 months, find 10 new springs, and estimate Tmax for 14 sites.By the end of 3 months we anticipate having water chemistry, isotope samples, gas samples, and Tmax determinations for 30 springs in the two study areas.

Thermochronometry using red TL of quartz - a feasibility study from in-situ drill-hole samples

NASA Astrophysics Data System (ADS)

Schmidt, Christoph; Zöller, Ludwig

2015-04-01

Thermochronometry - the revelation of the temperature history of rock related to subsidence or uplift and erosion - relies on methods with closure temperatures >40-70 °C, such as (U-Th-Sm)/He or fission track analysis on apatite. These methods are applicable to young and tectonically active mountain ranges, but results of calculated mean denudation rates are too imprecise for older orogens. Several studies attested the quartz luminescence signal (325 °C TL peak, OSL fast component) isothermal decay at ambient temperatures as low as 56 °C (Prokein and Wagner, 1994; Herman et al., 2010; de Sarkar et al., 2013). The so far determined closure temperatures of the quartz luminescence thermochronometry system vary between ~35 °C for the OSL fast component (Herman et al., 2010) and ~70 °C for red thermoluminescence (RTL; Tsuchiya and Fujino, 2000) and are dependent on the cooling rate and the charge trap parameters. Although featuring a favourably low closure temperature - thus allowing to study the geologically most recent temperature history -, especially quartz OSL suffers from low dose saturation, limiting the application to highly erosive orogens. Saturation doses of RTL exceed those of OSL by a factor of 10 or more (Fattahi and Stokes, 2000), what opens up new perspectives in low-temperature thermochronometry. We here present experimental results on the general suitability of RTL for thermochronometry, obtained for samples from a drilling hole in the granitic basement of the Variscan Fichtelgebirge (Franconia, Germany). The samples allowed studying the RTL signal saturation level in-situ at different ambient temperatures up to ~55 °C (at 1831 m depth). Measurements confirmed depletion of the 325 °C RTL peak for ambient temperatures >25 °C, most probably for even lower temperatures. Irradiation experiments showed that the RTL signal is not in saturation for ambient temperatures >25 °C, even for this 'old' mountain range. We could further demonstrate that the luminescence sensitivity of samples strongly increases with rising ambient temperature, opposite to the findings of Ypma and Hochman (1991) for samples from sedimentary basins. References Fattahi, M., Stokes, S., 2000. Extending the time range of luminescence dating using red TL (RTL) from volcanic quartz. Radiation Measurements 32, 479-485. Herman, F., Rhodes, E.J., Braun, J., Heiniger, L., 2010. Uniform erosion rates and relief amplitude during glacial cycles in the Southern Alps of New Zealand, as revealed from OSL-thermochronology. Earth and Planetary Science Letters 297, 183-189. Prokein, J., Wagner, G.A., 1994. Analysis of thermoluminescent glow peaks in quartz derived from the KTB-drill hole. Radiation Measurements 23, 85-94. de Sarkar, S., Mathew, G., Pande, K., Chauhan, N., Singhvi, A.K., 2013. Rapid denudation of Higher Himalaya during late Pleistocence, evidence from OSL thermochronology. Geochronometria 40, 304-310. Tsuchiya, N., Fujino, K., 2000. Evaluation of cooling history of the Quaternary Takidani pluton using thermoluminescence technique. Proceedings World Geothermal Congress, Kyushu-Tohoku, Japan. Ypma, P.J., Hochman, M.B., 1991. Thermoluminescence geothermometry - a case study of the Otway basin. APEA Journal, 312-324.

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.

Structural Inventory of Great Basin Geothermal Systems and Definition of Favorable Structural Settings

DOE Data Explorer

Faulds, James E.

2013-12-31

Over the course of the entire project, field visits were made to 117 geothermal systems in the Great Basin region. Major field excursions, incorporating visits to large groups of systems, were conducted in western Nevada, central Nevada, northwestern Nevada, northeastern Nevada, east‐central Nevada, eastern California, southern Oregon, and western Utah. For example, field excursions to the following areas included visits of multiple geothermal systems: - Northwestern Nevada: Baltazor Hot Spring, Blue Mountain, Bog Hot Spring, Dyke Hot Springs, Howard Hot Spring, MacFarlane Hot Spring, McGee Mountain, and Pinto Hot Springs in northwest Nevada. - North‐central to northeastern Nevada: Beowawe, Crescent Valley (Hot Springs Point), Dann Ranch (Hand‐me‐Down Hot Springs), Golconda, and Pumpernickel Valley (Tipton Hot Springs) in north‐central to northeast Nevada. - Eastern Nevada: Ash Springs, Chimney Hot Spring, Duckwater, Hiko Hot Spring, Hot Creek Butte, Iverson Spring, Moon River Hot Spring, Moorman Spring, Railroad Valley, and Williams Hot Spring in eastern Nevada. - Southwestern Nevada‐eastern California: Walley’s Hot Spring, Antelope Valley, Fales Hot Springs, Buckeye Hot Springs, Travertine Hot Springs, Teels Marsh, Rhodes Marsh, Columbus Marsh, Alum‐Silver Peak, Fish Lake Valley, Gabbs Valley, Wild Rose, Rawhide‐ Wedell Hot Springs, Alkali Hot Springs, and Baileys/Hicks/Burrell Hot Springs. - Southern Oregon: Alvord Hot Spring, Antelope Hot Spring‐Hart Mountain, Borax Lake, Crump Geyser, and Mickey Hot Spring in southern Oregon. - Western Utah: Newcastle, Veyo Hot Spring, Dixie Hot Spring, Thermo, Roosevelt, Cove Fort, Red Hill Hot Spring, Joseph Hot Spring, Hatton Hot Spring, and Abraham‐Baker Hot Springs. Structural controls of 426 geothermal systems were analyzed with literature research, air photos, google‐Earth imagery, and/or field reviews (Figures 1 and 2). Of the systems analyzed, we were able to determine the structural settings of more than 240 sites. However, we found that many “systems” consisted of little more than a warm or hot well in the central part of a basin. Such “systems” were difficult to evaluate in terms of structural setting in areas lacking in geophysical data. Developed database for structural catalogue in a master spreadsheet. Data components include structural setting, primary fault orientation, presence or absence of Quaternary faulting, reservoir lithology, geothermometry, presence or absence of recent magmatism, and distinguishing blind systems from those that have surface expressions. Reviewed site locations for all 426 geothermal systems– Confirmed and/or relocated spring and geothermal sites based on imagery, maps, and other information for master database. Many systems were mislocated in the original database. In addition, some systems that included several separate springs spread over large areas were divided into two or more distinct systems. Further, all hot wells were assigned names based on their location to facilitate subsequent analyses. We catalogued systems into the following eight major groups, based on the dominant pattern of faulting (Figure 1): - Major normal fault segments (i.e., near displacement maxima). - Fault bends. - Fault terminations or tips. - Step‐overs or relay ramps in normal faults. - Fault intersections. - Accommodation zones (i.e., belts of intermeshing oppositely dipping normal faults), - Displacement transfer zones whereby strike‐slip faults terminate in arrays of normal faults. - Transtensional pull‐aparts. These settings form a hierarchal pattern with respect to fault complexity. - Major normal faults and fault bends are the simplest. - Fault terminations are typically more complex than mid‐segments, as faults commonly break up into multiple strands or horsetail near their ends. - A fault intersection is generally more complex, as it generally contains both multiple fault strands and can include discrete di...

Deformation partitioning and fabric development during shearing of felsic migmatites (Valpelline Series, NW Alps)

NASA Astrophysics Data System (ADS)

Pariani, Federico; Menegon, Luca; Bistacchi, Andrea; Malaspina, Nadia

2014-05-01

The relationships between partial melting and deformation in the continental lower crust are critical for understanding lithosphere rheology and the processes leading to melt segregation. In metapelitic rocks in the lower portions of the crust partial melting typically occurs via dehydration of biotite and is generally characterized by a negative volume change when garnet is produced as a peritectic phase. As a result, segregation of biotite-derived melt by fracturing resulting from dilational strain is not common. Hence segregation of biotite-derived melts in the lower crust is likely to be controlled by active deformation via creation of structural anisotropies (fabric), which define migration pathways from the grain-size to the kilometre scale. This study investigates the relations between deformation mechanisms of minerals, fabric development and grain- and meso-scale deformation partitioning in felsic migmatites. The study area is located in the Valpelline Series of the Dent Blanche Nappe in the north-western Alps, which represents a slice of pre-Alpine lower crust dominated by metapelitic migmatites (i.e. 'kinzigites' in the Alpine literature). The migmatites are stromatic and show a leucosome-melanosome interlayering defining the dominant foliation (S2), which forms along a sinistral shear zone at least 1 km thick and laterally continuous for at least 8 km. Ti-in biotite geothermometry, mineral inclusions in garnet, and literature data indicate that S2 formed at P, T conditions of 800-820°C, 0.4-0.7 GPa, during dehydration melting of biotite. The melanosomes have about 80 vol% of garnet + biotite + sillimanite and are very poor in quartz and feldspars, indicating almost complete removal of melt. Garnet forms slightly elongated grains wrapped by biotite and sillimanite layers. Compositional maps of the elongated garnet do not show any zonation. EBSD analysis indicates that the elongated garnets are actually clusters of individual grains with no internal misorientation. We interpret these microstructures as deriving from amalgamation of individual garnets in elongated sites during shearing. Prismatic sillimanite has a strong crystallographic preferred orientation (CPO) with the c-axes parallel to the stretching lineation. However, evidence for internal misorientaton is scarce, indicating that the CPO was probably achieved by passive rotation during shearing. Elongated K-feldspar grains also do not show any internal misorientation and crystal plasticity features. They are rich of sillimanite and quartz inclusions, suggesting that they represent melt pockets crystallized near the site of production. K-feldspar has a weak CPO with the (010) planes parallel to the foliation and either <100> or <101> axis parallel to the lineation. The high aspect ratio was probably achieved by oriented growth during crystallization of melt. In summary, deformation mechanisms of minerals during melt removal from the melanosome seem to be dominated by passive rotation and oriented growth during magmatic flow, with negligible contribution of dislocation creep. A large (at least several hundred metres thick across foliation) low-strain domain of less pelitic, more quartzofeldspathic composition has escaped the pervasive development of S2. This domain preserves an S1 associated with older stages of partial melting. We speculate that the different bulk and mineralogical composition, reflecting the different nature of the protolith but also the effect of pre-existing melting episodes, determined a reduced melting during D2. This resulted in localization of deformation along melt-richer portions of this lower crustal section.

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

NASA Astrophysics Data System (ADS)

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

2015-10-01

;Clumped-isotope; thermometry is an emerging tool to probe the temperature history of surface and subsurface environments based on measurements of the proportion of 13C and 18O isotopes bound to each other within carbonate minerals in 13C18O16O22- groups (heavy isotope ;clumps;). Although most clumped isotope geothermometry implicitly presumes carbonate crystals have attained lattice equilibrium (i.e., thermodynamic equilibrium for a mineral, which is independent of solution chemistry), several factors other than temperature, including dissolved inorganic carbon (DIC) speciation may influence mineral isotopic signatures. Therefore we used a combination of approaches to understand the potential influence of different variables on the clumped isotope (and oxygen isotope) composition of minerals. We conducted witherite precipitation experiments at a single temperature and at varied pH to empirically determine 13C-18O bond ordering (Δ47) and δ18O of CO32- and HCO3- molecules at a 25 °C equilibrium. Ab initio cluster models based on density functional theory were used to predict equilibrium 13C-18O bond abundances and δ18O of different DIC species and minerals as a function of temperature. Experiments and theory indicate Δ47 and δ18O compositions of CO32- and HCO3- ions are significantly different from each other. Experiments constrain the Δ47-δ18O slope for a pH effect (0.011 ± 0.001; 12 ⩾ pH ⩾ 7). Rapidly-growing temperate corals exhibit disequilibrium mineral isotopic signatures with a Δ47-δ18O slope of 0.011 ± 0.003, consistent with a pH effect. Our theoretical calculations for carbonate minerals indicate equilibrium lattice calcite values for Δ47 and δ18O are intermediate between HCO3- and CO32-. We analyzed synthetic calcites grown at temperatures ranging from 0.5 to 50 °C with and without the enzyme carbonic anhydrase present. This enzyme catalyzes oxygen isotopic exchange between DIC species and is present in many natural systems. The two types of experiments yielded statistically indistinguishable results, and these measurements yield a calibration that overlaps with our theoretical predictions for calcite at equilibrium. The slow-growing Devils Hole calcite exhibits Δ47 and δ18O values consistent with lattice equilibrium. Factors influencing DIC speciation (pH, salinity) and the timescale for DIC equilibration, as well as reactions at the mineral-solution interface, have the potential to influence clumped-isotope signatures and the δ18O of carbonate minerals. In fast-growing carbonate minerals, solution chemistry may be an important factor, particularly over extremes of pH and salinity. If a crystal grows too rapidly to reach an internal equilibrium (i.e., achieve the value for the temperature-dependent mineral lattice equilibrium), it may record the clumped-isotope signature of a DIC species (e.g., the temperature-dependent equilibrium of HCO3-) or a mixture of DIC species, and hence record a disequilibrium mineral composition. For extremely slow-growing crystals, and for rapidly-grown samples grown at a pH where HCO3- dominates the DIC pool at equilibrium, effects of solution chemistry are likely to be relatively small or negligible. In summary, growth environment, solution chemistry, surface equilibria, and precipitation rate may all play a role in dictating whether a crystal achieves equilibrium or disequilibrium clumped-isotope signatures.

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

USGS Publications Warehouse

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

2015-01-01

“Clumped-isotope” thermometry is an emerging tool to probe the temperature history of surface and subsurface environments based on measurements of the proportion of 13C and 18O isotopes bound to each other within carbonate minerals in 13C18O16O22- groups (heavy isotope “clumps”). Although most clumped isotope geothermometry implicitly presumes carbonate crystals have attained lattice equilibrium (i.e., thermodynamic equilibrium for a mineral, which is independent of solution chemistry), several factors other than temperature, including dissolved inorganic carbon (DIC) speciation may influence mineral isotopic signatures. Therefore we used a combination of approaches to understand the potential influence of different variables on the clumped isotope (and oxygen isotope) composition of minerals.We conducted witherite precipitation experiments at a single temperature and at varied pH to empirically determine 13C-18O bond ordering (Δ47) and δ18O of CO32- and HCO3- molecules at a 25 °C equilibrium. Ab initio cluster models based on density functional theory were used to predict equilibrium 13C-18O bond abundances and δ18O of different DIC species and minerals as a function of temperature. Experiments and theory indicate Δ47 and δ18O compositions of CO32- and HCO3- ions are significantly different from each other. Experiments constrain the Δ47-δ18O slope for a pH effect (0.011 ± 0.001; 12 ⩾ pH ⩾ 7). Rapidly-growing temperate corals exhibit disequilibrium mineral isotopic signatures with a Δ47-δ18O slope of 0.011 ± 0.003, consistent with a pH effect.Our theoretical calculations for carbonate minerals indicate equilibrium lattice calcite values for Δ47 and δ18O are intermediate between HCO3− and CO32−. We analyzed synthetic calcites grown at temperatures ranging from 0.5 to 50 °C with and without the enzyme carbonic anhydrase present. This enzyme catalyzes oxygen isotopic exchange between DIC species and is present in many natural systems. The two types of experiments yielded statistically indistinguishable results, and these measurements yield a calibration that overlaps with our theoretical predictions for calcite at equilibrium. The slow-growing Devils Hole calcite exhibits Δ47 and δ18O values consistent with lattice equilibrium.Factors influencing DIC speciation (pH, salinity) and the timescale for DIC equilibration, as well as reactions at the mineral–solution interface, have the potential to influence clumped-isotope signatures and the δ18O of carbonate minerals. In fast-growing carbonate minerals, solution chemistry may be an important factor, particularly over extremes of pH and salinity. If a crystal grows too rapidly to reach an internal equilibrium (i.e., achieve the value for the temperature-dependent mineral lattice equilibrium), it may record the clumped-isotope signature of a DIC species (e.g., the temperature-dependent equilibrium of HCO3−) or a mixture of DIC species, and hence record a disequilibrium mineral composition. For extremely slow-growing crystals, and for rapidly-grown samples grown at a pH where HCO3- dominates the DIC pool at equilibrium, effects of solution chemistry are likely to be relatively small or negligible. In summary, growth environment, solution chemistry, surface equilibria, and precipitation rate may all play a role in dictating whether a crystal achieves equilibrium or disequilibrium clumped-isotope signatures.

Compositional zoning of the bishop tuff

USGS Publications Warehouse

Hildreth, W.; Wilson, C.J.N.

2007-01-01

Compositional data for >400 pumice clasts, organized according to eruptive sequence, crystal content, and texture, provide new perspectives on eruption and pre-eruptive evolution of the >4600 km3 of zoned rhyolitic magma ejected as the BishopTuff during formation of Long Valley caldera. Proportions and compositions of different pumice types are given for each ignimbrite package and for the intercalated plinian pumice-fall layers that erupted synchronously. Although withdrawal of the zoned magma was less systematic than previously realized, the overall sequence displays trends toward greater proportions of less evolved pumice, more crystals (0-5 24 wt %), and higher FeTi-oxide temperatures (714-818??C). No significant hiatus took place during the 6 day eruption of the BishopTuff, nearly all of which issued from an integrated, zoned, unitary reservoir. Shortly before eruption, however, the zoned melt-dominant portion of the chamber was invaded by batches of disparate lower-silica rhyolite magma, poorer in crystals than most of the resident magma but slightly hotter and richer in Ba, Sr, andTi. Interaction with resident magma at the deepest levels tapped promoted growth ofTi-rich rims on quartz, Ba-rich rims on sanidine, and entrapment of near-rim melt inclusions relatively enriched in Ba and CO2.Varied amounts of mingling, even in higher parts of the chamber, led to the dark gray and swirly crystal-poor pumices sparsely present in all ashflow packages. As shown by FeTi-oxide geothermometry, the zoned rhyolitic chamber was hottest where crystal-richest, rendering any model of solidification fronts at the walls or roof unlikely.The main compositional gradient (75-195 ppm Rb; 0.8-2.2 ppm Ta; 71-154 ppm Zr; 0.40-1.73% FeO*) existed in the melt, prior to crystallization of the phenocryst suite observed, which included zircon as much as 100 kyr older than the eruption.The compositions of crystals, though themselves largely unzoned, generally reflect magma temperature and the bulk compositional gradient, implying both that few crystals settled or were transported far and that the observed crystals contributed little to establishing that gradient. Upward increases in aqueous gas and dissolved water, combined with the adiabatic gradient (for the 5 km depth range tapped) and the roofward decline in liquidus temperature of the zoned melt, prevented significant crystallization against the roof, consistent with dominance of crystal-poor magma early in the eruption and lack of any roof-rind fragments among the Bishop ejecta, before or after onset of caldera collapse. A model of secular incremental zoning is advanced wherein numerous batches of crystal-poor melt were released from a mush zone (many kilometers thick) that floored the accumulating rhyolitic melt-rich body. Each batch rose to its own appropriate level in the melt-buoyancy gradient, which was selfsustaining against wholesale convective re-homogenization, while the thick mush zone below buffered it against disruption by the deeper (non-rhyolitic) recharge that augmented the mush zone and thermally sustained the whole magma chamber. Crystal-melt fractionation was the dominant zoning process, but it took place not principally in the shallow melt-rich body but mostly in the pluton-scale mush zone before and during batchwise melt extraction. ?? Published by Oxford University Press (2007).

Early postcaldera rhyolite and structural resurgence at Long Valley Caldera, California

NASA Astrophysics Data System (ADS)

Hildreth, Wes; Fierstein, Judy; Calvert, Andrew

2017-04-01

After the 767-ka caldera-forming eruption of 650 km3 of rhyolite magma as the Bishop Tuff, 90-100 km3 of similar rhyolite erupted in the west-central part of Long Valley caldera in as many as 40 batches spread over the 110,000-year interval from 750 ka to 640 ka. Centrally, this Early Rhyolite (ER) is as thick as 622 m, but it spread radially to cover much of the caldera floor, where half its area is now concealed by post-ER sediments and lavas. At least 75% of the ER is aphyric rhyolite tuff. Drillholes encountered 22 (altered) ER lava flows intercalated in the pyroclastic pile, and another 11 units of (largely fresh) ER lava are exposed on the caldera's resurgent dome and at Lookout Mountain. Exposed units have been distinguished, mapped, studied petrographically and chemically, and radioisotopically dated; each is described in detail. Their phenocryst contents range from 0 to 2.5 wt%. All the phyric units have plagioclase, orthopyroxene, and ilmenite; most have biotite and rare tiny magnetite, and a few contain rare zircon. The compositional range of fresh obsidians is narrow-74.3-75.0% SiO2, 1.21-1.37% FeO*, and 5.12-5.26% K2O, but wider variations in Ti, Ba, Sr, and Zr permit distinction of individual units and eruptive groups. The limited chemical and petrographic variability shown by so many ER batches released episodically for 110,000 years suggests a thermally buffered and well-stirred reservoir. The ER central area, where ER eruptions had taken place, was uplifted 400 m to form a structural dome 10 km in diameter. Most of the inflation is attributable to 10 sills of ER that intrude the Bishop Tuff beneath the uplift, but other processes potentially contributing to resurgence are also considered. As shown by erratics of Mesozoic rocks ice-rafted from the Sierra Nevada and dropped on ER lavas, much of the ER had erupted early enough and at low enough elevation to be inundated by the intracaldera lake and was only later lifted by the resurgence that also raised clusters of the erratics hundreds of meters higher than any shoreline. Most of the uplift was over by 570 ka, but dome-crossing faults that exhibit normal throw of 10-30 m cut lavas as young as 175-125 ka. For most elements, chemical ranges of the ER lie within those of the zoned Bishop Tuff, which had erupted earlier from the same place. Only Ba, Zr, Hf, and Eu/Eu* extend to ranges outside those of the Bishop Tuff, nominally to less evolved compositions. Initial 87Sr/86Sr values of ER are likewise within the range of the Bishop Tuff, but ER ratios of 143Nd/144Nd and 206Pb/204Pb extend beyond those of the Bishop Tuff to values slightly more influenced by upper-crustal contributions. FeTi-oxide geothermometry yields 752°-844 °C for ER, compared to 700°-820 °C for the Bishop Tuff. ER fO2 values are 0.5-1.0 log units more reduced than those of the T-fO2 array of the Bishop Tuff. The postcaldera reduction may reflect reaction with graphite from the black lithics of Paleozoic graphitic metapelite so abundant in the Bishop Tuff. Much of the pumice emplaced during the later half of the Bishop Tuff eruption has 10-25 wt% phenocrysts, dominantly quartz and sanidine, but the 100 km3 of ER has only 0-2.5 wt% and completely lacks quartz and sanidine. Postcaldera processes, including mixing, volatile ascent, and crystal resorption, as well as potential contaminants and magmatic inputs, are all considered.

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

Pumpernickel Valley Geothermal Project Thermal Gradient Wells

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

Z. Adam Szybinski

2006-01-01

The Pumpernickel Valley geothermal project area is located near the eastern edge of the Sonoma Range and is positioned within the structurally complex Winnemucca fold and thrust belt of north-central Nevada. A series of approximately north-northeast-striking faults related to the Basin and Range tectonics are superimposed on the earlier structures within the project area, and are responsible for the final overall geometry and distribution of the pre-existing structural features on the property. Two of these faults, the Pumpernickel Valley fault and Edna Mountain fault, are range-bounding and display numerous characteristics typical of strike-slip fault systems. These characteristics, when combined withmore » geophysical data from Shore (2005), indicate the presence of a pull-apart basin, formed within the releasing bend of the Pumpernickel Valley – Edna Mountain fault system. A substantial body of evidence exists, in the form of available geothermal, geological and geophysical information, to suggest that the property and the pull-apart basin host a structurally controlled, extensive geothermal field. The most evident manifestations of the geothermal activity in the valley are two areas with hot springs, seepages, and wet ground/vegetation anomalies near the Pumpernickel Valley fault, which indicate that the fault focuses the fluid up-flow. There has not been any geothermal production from the Pumpernickel Valley area, but it was the focus of a limited exploration effort by Magma Power Company. In 1974, the company drilled one exploration/temperature gradient borehole east of the Pumpernickel Valley fault and recorded a thermal gradient of 160oC/km. The 1982 temperature data from five unrelated mineral exploration holes to the north of the Magma well indicated geothermal gradients in a range from 66 to 249oC/km for wells west of the fault, and ~283oC/km in a well next to the fault. In 2005, Nevada Geothermal Power Company drilled four geothermal gradient wells, PVTG-1, -2, -3, and -4, and all four encountered geothermal fluids. The holes provided valuable water geochemistry, supporting the geothermometry results obtained from the hot springs and Magma well. The temperature data gathered from all the wells clearly indicates the presence of a major plume of thermal water centered on the Pumpernickel Valley fault, and suggests that the main plume is controlled, at least in part, by flow from this fault system. The temperature data also defines the geothermal resource with gradients >100oC/km, which covers an area a minimum of 8 km2. Structural blocks, down dropped with respect to the Pumpernickel Valley fault, may define an immediate reservoir. The geothermal system almost certainly continues beyond the recently drilled holes and might be open to the east and south, whereas the heat source responsible for the temperatures associated with this plume has not been intersected and must be at a depth greater than 920 meters (depth of the deepest well – Magma well). The geological and structural setting and other characteristics of the Pumpernickel Valley geothermal project area are markedly similar to the portions of the nearby Dixie Valley geothermal field. These similarities include, among others, the numerous, unexposed en echelon faults and large-scale pull-apart structure, which in Dixie Valley may host part of the geothermal field. The Pumpernickel Valley project area, for the majority of which Nevada Geothermal Power Company has geothermal rights, represents a geothermal site with a potential for the discovery of a relatively high temperature reservoir suitable for electric power production. Among locations not previously identified as having high geothermal potential, Pumpernickel Valley has been ranked as one of four sites with the highest potential for electrical power production in Nevada (Shevenell and Garside, 2003). Richards and Blackwell (2002) estimated the total heat loss and the preliminary production capacity for the entire Pumpernickel Valley geothermal system to be at 35MW. A more conservative estimate, for the hot spring area only, was presented by GeothermEx Inc. (2004), which projected that power generation capacities for the Pumpernickel Valley site are 10 MW-30yrs minimum (probablility of >90%), and most likely 13 MW-30yrs.« less

BARRINGER AWARD ADDRESS: Shock Metamorphism of Quartz in Nature and Experiment: A Review

NASA Astrophysics Data System (ADS)

Stoffler, D.

1993-07-01

Quartz as a widespread rock-forming mineral of the Earth's crust represents the most sensitive indicator of impact-induced shock waves and therefore provides an outstanding tool for the recognition of terrestrial impact formations and for the pressure calibration of shock metamorphosed rocks. This paper attempts to summarize the current knowledge in this field. Shocked quartz has been observed in quite variable spatial relations to impact craters: (1) in the crater basement, (2) in rock and mineral clasts of polymict breccias, and (3) in distal ejecta such as tektites and global air- fall beds (e.g., K/T boundary). Quartz displays a wide variety of shock- induced mechanical deformations and transformations [1,2]. Microscopically observable effects are multiple sets of planar fractures (PF) and planar deformation features (PDF) parallel to low indices crystallographic planes; mosaickism; reduced refractivity and birefringence; partial transformation to stishovite; increased optic axial angle; amorphization (diaplectic glass), partial transformation to coesite; and melting (lechatelierite). Additional effects at the atomic scale are well documented by TEM, X-ray diffraction and spectroscopy [3-7]. All types of shock effects observed so far in natural quartz have been reproduced by experimental shock waves in the laboratory and in large scale TNT and nuclear explosions. By means of sophisticated techniques the pressure dependence of shock effects has been calibrated with high precision. Threshold pressures at room temperature (given in GPa) for the onset of certain effects in single crystals and in nonporous quartzofeldpathic rocks are: 7.5 +- 2, 10 +- 2, 20 +- 2 (various PFs and PDFs), 12 +- 1 (stishovite), 25 +- 1 (reduced refractive index and density), ~30 (coesite), 34 +- 1 (total transformation to diaplectic glass), 50 +- 2 (melting and formation of lechatelierite) [8-12]. The type of shock effects, their paragenetic combination, and their formation pressure are strongly dependent on the physical and textural properties of the impacted quartz-bearing target. Porosity [13] and preshock temperature [9,12,14] are most effective. Both properties are lowering the threshold pressure for certain shock effects and they affect the orientation and type of planar deformation structures (PFs and PDFs). Upon thermometamorphism shocked quartz displays characteristic annealing effects useful for (limited) geothermometry. PDFs transform to "decorated planar features" due to recrystallization. These features persist up to the conditions of recrystallization of the primary quartz. Annealing of diaplectic glass leads to densification of the glass between 700 and 1200 degrees C and to complete recrystallization to alpha-quartz + alpha-cristobalite above 1200 degrees C [10]. In impact craters this transformation produces the characteristic "ballen" texture as observed in clasts of melt rocks. Stishovite and coesite decompose near 350 degrees C and above about 1150 degrees C, respectively. These annealing features provide important boundary conditions for interpreting the temperature-time history of impact formations. There is unequivocal evidence, strongly supported by TEM studies [3,4,8], that most of the shock effects discussed above and, certainly, the complete set cannot be produced by endogenic processes in near-surface environments of the Earth's crust where the strain rates are several orders of magnitude lower than those in impact processes, and the peak pressures exceed 5 GPa only in very special tectonic settings at great depth. References: [1] Stoffler D. (1972) Fortschr. Mineral., 49, 50-113, and references therein. [2] Stoffler D. (1974) Fortschr. Mineral., 51, 256-289. [3] Gratz A. J. et al. (1988) Phys. Chem. Mineral., 16, 221-233. [4] Goltrant O. et al. (1991) EPSL 106, 103-115. [5] Cygan R. T. et al. (1990) LPSC XX, 451-457. [6] Jakubith M. and Lehmann G. (1981) Phys. Chem. Mineral., 7, 165- 168. [7] Ashworth J. R. and Schneider H. (1985) Phys. Chem. Mineral., 11, 241- 249. [8] Stoffler D. (1984) J. Non-Cryst. Solids, 67, 465-502, and references therein. [9] Gratz A. J. (1992) Phys. Chem. Mineral., 19, 267-288, [10] Rehfeldt-Oskierski A. (1986) Ph.D. thesis, Univ. of Munster. [11] Grothues J. (1988) Diploma thesis, Univ. of Muenster [12] Langenhorst F. (1993), Ph.D. thesis, Univ. of Munster. [13] Kieffer S. W. et al. (1976) Contr. Mineral. Petrol., 59, 41-93, [14] Langenhorst F. (1992) Nature, 356, 507-509.