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Geology topics

A.H. Truesdell

Publications and source records attributed to A.H. Truesdell.

At least 19 recordsLinked to original sources
USGS2012

Reservoir processes and fluid origins in the Baca geothermal system, Valles Caldera, New Mexico

At the Baca geothermal field in the Valles caldera, New Mexico, 19 deep wells were drilled in an attempt to develop a 50-MW e (megawatts electric) power plant. The chemical and isotopic compositions of steam and water samples have been used to indicate uniquely the origin of reservoir fluids and natural reservoir processes. Two distinct reservoir fluids exist at Baca. These fluids originate from the same deep, high-temperature (335°C), saline (2500 mg/kg Cl) parent water but have had different histories during upflow. One fluid (from wells 4 and 13) is isotopically light, high in radiogenic noble gases, CO 2 and HCO 3 , and low in Ca. It has a temperature of 290°–295°C and a reservoir chloride near 1900 mg/kg. This fluid resulted from rapid upward flow through 1.1- to 1.4-m.y.-old Bandelier Tuff reservoir rocks after long residence in pre-Bandelier (>7 m.y.) sediments and Precambrian basement rocks and 25% dilution with high-altitude cold groundwater from Redondo Peak. The other water (from wells 15, 19, and 24) moved slowly through the Bandelier Tuff and cooled conductively (with minor steam loss for well 19) from 335°C to 280°–260°C. Apparently, short residence in old basement rocks has left this water with low radiogenic gases. Conductive cooling without mixing has kept the original chloride and relatively heavy isotope composition of the deep water. The recharge to the deep parent water is not well understood but may be from lower elevation precipitation outside the Valles caldera area. Gases are in equilibrium in all-liquid reservoir fluids at near reservoir temperatures, and the concentrations of atmospheric gases are similar to those of air-saturated water, indicating little boiling and steam loss. All water, solutes, and gases in the reservoir fluids originate from air-saturated meteoric recharge water, watermineral reactions, and rock leaching, with the possible exception of excess 3He that must have an ultimate mantle source. This gas could originate directly from magma or from leaching of intrusive volcanic rocks beneath the Bandelier.

Journal of Geophysical Research Solid Earth↗
USGS1992

Geothermal gas compositions in yellowstone National Park, USA

Gas samples collected between 1974 and 1986 have been analysed for the ten major components. Samples have been collected almost exclusively from the tops of pools, which has degraded the value of the data, and limited inter-comparisons to the relatively insoluble components, Ar, N2, CH4, H2 and He. A general gas distribution pattern in the park, in terms of these components, shows the major heat source(s) to underlie the Gibbon and Mud Volcano areas with all other geothermal areas having gas compositions consistent with a general north-south water flow. Shoshone Basin gases show a large range of compositions and these are analysed in detail. The patterns conform to that which would be expected from an east-west flow or fluid with progressive boiling and subsequent dilution. ?? 1992.

Journal of Volcanology and Geothermal Research↗
USGS1991

Pre-exploitation state of the Ahuachapán geothermal field, El Salvador

The lithology and structural features of the Ahuachapán geothermal area and their impact on the movement of cold and hot fluids within the system are described, as well as the development and evaluation of the natural state model of the field. Four major lithologic units are present in Ahuachapán and three major aquifers have been identified; flow patterns and zones of fluid mixing were located on the basis of temperature and geochemical data from wells and surface manifestations. Geologic structures control the heat and fluid recharge and the flow within the reservoir. Modeling studies suggest, in agreement with field data, an overall average transmissivity of 25–35 darcy-meters, and indicate that the system is recharged by waters with temperatures greater than 250°C. The total thermal throughflow for the Ahuachapán reservoir in the unexploited state is estimated to be about 250 MW t .

Geothermics↗
USGS1991

A review of the hydrogeologic-geochemical model for Cerro Prieto

With continued exploitation of the Cerro Prieto, Mexico, geothermal field, there is increasing evidence that the hydrogeologic model developed by Halfman and co-workers presents the basic features controlling the movement of geothermal fluids in the system. In mid–1987 the total installed capacity at Cerro Prieto reached 620 MW c , requiring a large rate of fluid production (more than 10,500 tonnes/hr of a brine-steam mixture; August 1988). This significant mass extraction has led to changes in reservoir thermodynamic conditions and in the chemistry of the produced fluids. Pressure drawdown has caused an increase in cold water recharge in the southern and western edges of the field, and local and general reservoir boiling in parts of the geothermal system. After reviewing the hydrogeologic and geochemical models of Cerro Prieto, the exploitation-induced cold water recharge and reservoir boiling (and plugging) observed in different areas of the field, are discussed and interpreted on the basis of these models and schematic flow models that describe the hydrogeology.

Geothermics↗
USGS1991

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

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

Journal of Volcanology and Geothermal Research↗
USGS1991

A geochemical model of the Platanares geothermal system, Honduras

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

Journal of Volcanology and Geothermal Research↗
USGS1990

Coupled variations in helium isotopes and fluid chemistry: Shoshone Geyser Basin, Yellowstone National Park

Early studies of 3 He/ 4 He variations in geothermal systems have generally attributed these fluctuations to either differences in the source of the magmatic 3 He-rich helium or to local differences in the deep flux of magmatic 3 He-rich helium. Kennedy et al. (1987), however, show that near-surface processes such as boiling and dilution may also drastically affect 3 He 4 "> 3 He 4 He ratios of geothermal vapors. Helium isotope ratios were determined for several hot springs at Shoshone Geyser Basin of Yellowstone National Park for this study, along with other noble gas data. Stable isotope data and water and gas chemistry data for each spring were also compiled. The water chemistry indicates that there is one deep, hot thermal water in the area which is mixing with dilute meteoric water that has entered the system at depth. Spring HCO 3 − concentrations correlate with 3 He 4 He "> 3 He 4 He values, as in nearby Lower Geyser Basin. This correlation is attributed to variable amounts of deep dilution of thermal waters with a relatively cool water that inhibits boiling at depth, thus preventing the loss of CO 2 (and therefore HCO 3 − ) and magmatic He in the most diluted samples. Oxygen and hydrogen isotope data also support a boiling and dilution model, but to produce the observed fractionations, the boiling event would have to be extensive, with steam loss at the surface, whereas the boiling that affected the helium isotope ratios was probably a small scale event with steam loss at depth. It is possible that deep boiling occurred in the basin and that small amounts of steam escaped along fractures at about 500 m below the surface while all subsequently produced steam was lost near or at the surface.

Geochimica et Cosmochimica Acta↗
USGS1989

Origin and transport of chloride in superheated geothermal steam

Hydrogen chloride (HCl) is a known component of some volcanic gases and volcanic-related hydrothermal systems. It has recently been discovered in superheated steam in exploited geothermal systems, usually as a result of HCl-induced corrosion of well casing and steam gathering systems. Evaluation of four geothermal systems (Tatun, Taiwan; Krafla, Iceland; Larderello, Italy and The Geysers, USA) which produce CI-bearing steam provides evidence for the presence of Cl as HCl and the natural reservoir conditions which can produce HCl-bearing steam. Theoretical calculations defining the physical and chemical conditions of the reservoir liquid which can produce HCl-bearing steam are presented. The main factors are pH, temperature and Cl concentration. Lower pH, higher temperature and higher chlorinity allow more HCl to be volatilized with steam. In order to reach the surface in steam, the HCl cannot contact liquid water in which it is more soluble, essentially limiting transport to superheated steam. Temperature, pH and Cl concentration of reservoir liquids in each of the geothermal systems evaluated combine differently to produce HCl-bearing steam.

Geothermics↗
USGS1989

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

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.

Conference Paper↗
USGS1988

Carbon isotope geochemistry of hydrocarbons in the Cerro Prieto geothermal field, Baja California Norte, Mexico

Hydrocarbon abundances and stable-isotopic compositions were measured in wells M5, M26, M35 and M102, which represent a range of depths (1270-2000 m) and temperatures (275-330??C) in the field. In order to simulate the production of the geothermal hydrocarbons, gases were collected from the pyrolysis of lignite in the laboratory. This lignite was obtained from a well which sampled rock strata which are identical to those occurring in the field, but which have experienced much lower subsurface temperatures. In both the well and the laboratory observations, high-temperature environments favored higher relative concentrations of methane, ethane and benzene and generally higher ??13C-values in the individual hydrocarbons. The best correlation between the laboratory and well data is obtained when laboratory-produced gases from experiments conducted at lower (400??C) and higher (600??C) temperatures are mixed. This improved correlation suggests that the wells are sampling hydrocarbons produced from a spectrum of depths and temperatures in the sediments. ?? 1988.

Chemical Geology↗
USGS1985

A GC-system for the analysis of residual geothermal gases

The gases evolved from geothermal fields, after condensation of H2O, CO2, H2S and NH3 in caustic solution, contain He, H2, Ar, O2, N2, CH4 and higher hydrocarbons. The analysis for the major components in these residual gas mixtures can be achieved by use of two simple gas chromatographs in parallel, and using 5A?? molecular sieve. The separation of He and H2 to baseline is achieved by using low temperatures (30??C) coupled with a relatively long column; and the difficult separation of Ar and O2 is achieved by use of a cryogenically cooled column. The use of switching valves to backflush and bypass columns ensures that a minimum time for analysis can be achieved whilst retaining baseline separations of the He/H2 and Ar/O2 pairs. ?? 1985 Friedr. Vieweg & Sohn Verlagsgesellschaft mbH.

Chromatographia↗
USGS1985

CHEMISTRY OF LOW-TEMPERATURE GEOTHERMAL WATERS AT KLAMATH FALLS, OREGON.

Chemical and isotopic analyses of well discharges indicate that in the aquifer mixing occurs between shallow cold groundwater containing 2. 0 TU tritium and a deeper tritium-free thermal groundwaer at 100 to 120 degree C. This deeper water apparently results from the mixing of old, tritium-free cold groundwater and deep thermal groundwater at about 190 degree C and 120 mg/kg Cl. The temperature and chlorinity of the deep thermal water are based on SO//4-isotope and silica geothermometers and chloride and silica mixing models.

Conference Paper↗
USGS1984

A review of progress in understanding the fluid geochemistry of the Cerro Prieto geothermal system

Fluid geochemistry has played a major role in our present understanding of the Cerro Prieto geothermal system. Fluid chemical and isotopic compositions have been used to indicate the origin of water, salts and gases, original subsurface temperature and fluid flow, fluid-production mechanisms, and production-induced aquifer boiling and cold-water entry. The extensive geochemical data and interpretations for Cerro Prieto published from 1964 to 1981 are reviewed and discussed. Fluid geochemistry must continue to play an important role in the further development of the Cerro Prieto field. ?? 1984.

Geothermics↗
USGS1984

Dynamics of a geothermal field traced by noble gases: Cerro Prieto, Mexico

Noble gases have been measured mass spectrometrically in samples collected during 1977 from producing wells at Cerro Prieto. Positive correlations between concentrations of radiogenic (He and 40Ar) and atmospheric noble gases (Ne, Ar and Kr) suggest the following dynamic model: the geothermal fluids originated from meteoric water that penetrated to more than 2500 m depth (below the level of first boiling) and mixed with radiogenic He and 40Ar formed in the aquifer rocks. Subsequently, small amounts of steam were lost by a Raleigh process (0 - 30%) and mixing with shallow cold water occurred (0 - 30%). Noble gases are sensitive tracers of boiling in the initial stages of 0 - 3% steam separation and complement other tracers, such as C1 or temperature, which are effective only beyond this range. ?? 1984.

Geothermics↗
USGS1984

Production induced boiling and cold water entry in the Cerro Prieto geothermal reservoir indicated by chemical and physical measurements

Chemical and physical data suggest that the relatively shallow, western part of the Cerro Prieto reservoir is bounded below by low permeability rocks, and above and at the sides by an interface with cooler water. There is no continuous permeability barrier around or immediately above the reservoir. Permeability within the reservoir is dominantly intergranular. Mixture with cooler water rather than boiling is the dominant cooling process in the natural state, and production causes displacement of hot water by cooler water, not by vapour. Local boiling occurs near most wells in response to pressure decreases, but no general vapour zone has formed. ?? 1984.

Geothermics↗
USGS1983

Isotopic and chemical composition of Parbati Valley geothermal discharges, north-west Himalaya, India

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

Geothermics↗
USGS1983

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

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

Journal of Volcanology and Geothermal Research↗