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N.L. Nehring

Publications and source records attributed to N.L. Nehring.

14 recordsLinked to original sources
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

Stable-isotope evidence for a magmatic component in fumarole condensates from Augustine Volcano, Cook Inlet, Alaska, U.S.A.

D/H and 18O 16O ratios have been determined for fumarole condensates from Augustine Volcano, an active calc-alkaline stratovolcano in Lower Cook Inlet, Alaska. The isotopic data for the condensates form a linear ?? D-?? 18O array from low-temperature fluids (< 100??C) which are essentially local meteoric water (?? D {reversed tilde equals} -150???, ?? 18O {reversed tilde equals} -19???) to high-temperature (>450??C) fluids collected at the volcano summit which are enriched in both D and 18O (?? D {reversed tilde equals} -35???, ?? 18O {reversed tilde equals} +3.5???). Several lines of evidence suggest that the D-and 18O-rich condensates likely are "magmatic" fluids released into the hydrothermal system during and immediately after the 1976 eruption. Prior to 1976, the Augustine hydrothermal system was dominated completely by local meteoric waters. Between 1976 and 1982, fumarole condensates were observed to be variable mixtures of the "magmatic" fluid and meteoric water, with the proportion of the former systematically decreasing as the hydrothermal system cooled following the 1976 eruption. ?? 1985.

Chemical Geology↗
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

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

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

Geothermics↗
USGS1982

Chemical and light-stable isotope characteristics of waters from the Raft River geothermal area and environs, Cassia County, Idaho; Box Elder County, Utah

Chemical and light-stable isotope data are presented for water samples from the Raft River geothermal area and environs. On the basis of chemical character, as defined by a trilinear plot of per cent milliequivalents, and light-stable isotope data, the waters in the geothermal area can be divided into waters that have and have not mixed with cold water. The non-mixed waters have essentially a constant value of light-stable isotopes but show a large variation in chloride content. The variation of chloride composition is not the usual pattern for deep geothermal waters, where it is normally assumed that the deep water has a single chloride composition. Different mixed waters also have hot-water sources of varying chloride composition. Plots of chloride values on cross-sections show that water circulation patterns are confused, with non-mixed waters having different chloride concentrations located in close proximity. Three models can explain the characteristics of the deep geothermal water: (1) in addition to near-surface mixing of cold and hot water, there is deep mixing of two hot waters with the same enthalpy and isotopic composition but differing chloride concentrations to produce the range of chloride concentrations found in the deep geothermal water; (2) there is a single deep hot water, and the range of chloride concentrations is produced by the water passing through a zone of highly soluble materials (most likely in the sedimentary section above the basement) in which waters have different residence times or slightly different circulation paths; (3) the varying chloride concentrations in space have been caused by varying chloride concentrations in the deep feed water through time. Some of this older water has not been flushed from the system by the natural discharge. Although one model may seem more plausible than the others, the available data do not rule out any of them. Data for water samples from the Raft River and Jim Sage Mountains show that water from these areas is probably the source for the cold mixing water determined from end-members on mixing lines. Data for water samples in the Upper Raft River Valley show that the thermal anomaly found at Almo 1 is probably not related to the Raft River geothermal area. The water is different in type as shown by its placement on a trilinear plot, and the isotopes are different enough to show that it is probably a different water. Isotopic compositions of samples from a wide area around the Raft River geothermal system indicate that the likely source of the recharge water is the southern Albion Mountains and western Raft River Mountains. The recharge area is at one end of the Narrows zone, and the geothermal area is along the Narrows zone; thus it is likely that the Narrows zone defines the circulation path.

Geothermics↗
USGS1981

The origin of the Cerro Prieto geothermal brine

The Cerro Prieto geothermal brine may have originated from mixing of Colorado River water with seawater evaporated to about six times its normal salinity. This mixture circulated deeply and was heated by magmatic processes. During deep circulation, Li, K, Ca, B, SiO 2 and rare alkalis were transferred from rock minerals to the water, and Mg, SO 4 , and a minor quantity of Na were transferred to the rock. Similar alteration of seawater salt chemistry has been observed in coastal geothermal systems and produced in laboratory experiments. After heating and alteration the brine was further diluted to its present range of composition. Oxygen isotopes in the fluid are in equilibrium with reservoir calcite and have been affected by exploitation-induced boiling and dilution.

Geothermics↗
USGS1981

Molecular carbon isotopic evidence for the origin of geothermal hydrocarbons

Previous interest in light hydrocarbons from geothermal systems has focused principally on the origin of the methane1 and the estimation of subsurface temperatures from the carbon isotopic content of coexisting methane and carbon dioxide1-3. Higher molecular weight hydrocarbons were first reported in gases from Yellowstone National Park4, and have since been found to occur commonly in geothermal emanations in the western United States5. Isotopic measurements of individual geothermal hydrocarbons are now reported which help to explain the origin of these hydrocarbons. The thermal decomposition of sedimentary or groundwater organic matter is a principal source of hydrocarbons in four geothermal areas in western North America. ?? 1981 Nature Publishing Group.

Nature↗
USGS1979

Preliminary isotopic studies of fluids from the Cerro Prieto geothermal field

Preliminary isotopic studies of Cerro Prieto geothermal fluids and earlier studies of Mexicali Valley ground waters suggest local recharge of the geothermal system from the area immediately to the west. Oxygen isotope exchange of water with reservoir rock minerals at temperatures increasing with depth has produced fluids with oxygen-18 contents increasing with depth, and pressure drawdown in the southeastern part of the field has allowed lower oxygen-18 fluids to invade the production aquifer from above. The contents of tritium and carbon-14 in the fluid suggest only that the age of the fluid is between 50 and 10,000 years. The isotopic compositions of carbon and sulfur are consistent with a magmatic origin of these elements but a mixed sedimentary-organic origin appears more likely for carbon and is also possible for sulfur. Investigations of the isotopic compositions of geothermal and cold ground waters continue and are being expanded as fluids become available and as separation and analysis methods are improved. ?? 1979.

Geothermics↗
USGS1979

Gases in steam from Cerro Prieto geothermal wells with a discussion of steam/gas ratio measurements

As part of a joint USGS-CFE geochemical study of Cerro Prieto, steam samples were collected for gas analyses in April, 1977. Analyses of the major gas components of the steam were made by wet chemistry (for H2O,CO2,H2S and NH3) and by gas chromatography (He,H2,Ar,O2,N2 and hydrocarbons). The hydrocarbon gases in Cerro Prieto steam closely resemble hydrocarbons in steam from Larderello, Italy and The Geysers, California which, although they are vapor-dominated rather than hot-water geothermal systems, also have sedimentary aquifer rocks. These sedimentary geothermal hydrocarbons are characterized by the presence of branched C4-6 compounds and a lack of unsaturated compounds other than benzene. Relatively large amounts of benzene may be characteristic of high-temperature geothermal systems. All hydrocarbons in these gases other than methane most probably originate from the thermal metamorphosis of organic matter contained in the sediments. ?? 1979.

Geothermics↗
USGS1978

Gases and water isotopes in a geochemical section across the Larderello, Italy, geothermal field

Steam samples from six wells (Colombaia, Pineta, Larderello 57, Larderello 155, Gabbro 6, and Gabbro 1) in a south to north section across the Larderello geothermal field have been analyzed for inorganic and hydrocarbon gases and for oxygen-18 and deuterium of steam. The wells generally decrease in depth and increase in age toward the south. The steam samples are generally characterized by (1) Total gas contents increasing south to north from 0.003 to 0.05 mole fraction; (2) Constant CO2 (95??2 percent); near constant H2S (1.6??0.8), N2 (1.2??0.8), H2 (2??1), CH4 (1.2??1), and no O2 in the dry gas; (3) Presence of numerous, straight chain and branched C2 to C6 hydrocarbons plus benzene in amounts independent of CH4 contents with highest concentrations in the deeper wells; (4) Oxygen-18 contents of steam increasing south to north from -5.0??? to -0.4??? with little change in deuterium (-42??2???). These observations are interpreted as showing: (1) Decreasing gas contents with amount of production because the proportion of steam boiled from liquid water increases with production; (2) Synthesis of CH4 from H2 and CO2 with CO2 and H2 produced by thermal metamorphism and rock-water reactions; (3) Extraction of C2 to C6 hydrocarbons from rock organic matter; (4) Either oxygen isotope exchange followed by distillation of steam from the north toward the south (2 plates at ???220??C) or mixture of deeper more-exchange waters from the north with shallow, less-exchanged recharging waters from the south. ?? 1978 Birkha??user Verlag.

Pure and Applied Geophysics PAGEOPH↗
USGS1977

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

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

Geothermics↗