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I. Friedman

Publications and source records attributed to I. Friedman.

At least 37 records · Page 2Linked to original sources

Studies of quaternary saline lakes-II. Isotopic and compositional changes during desiccation of the brines in Owens Lake, California, 1969-1971

Owens Lake is an alkaline salt lake in a closed basin in southeast California. It is normally nearly dry, but in early 1969, an abnormal runoff from the Sierra Nevada flooded it to a maximum depth of 2·4 m. By late summer of 1971, the lake was again nearly dry and the dissolved salts recrystallized. Changes in the chemistry, pH, and deuterium content were monitored during desiccation. During flooding, salts (mostly trona, halite, and burkeite) dissolved slowly from the lake floor. Their concentration in the lake waters increased as evaporation removed water and salts again crystallized, but winter temperatures caused precipitation of some salts and the following summer warming caused their solution, resulting in seasonal variations in the concentration patterns of some ions. The pH values (9·4–10·4) changed with time but showed no detectable diurnal pattern. The deuterium concentration increased during evaporation and appeared to be in equilibrium with vapor leaving the lake according to the Rayleigh equation. The effective α(D/H in liquid/D/H in vapor) decreased as salinity increased; the earliest measured value was 1·069 [as total dissolved solids (TDS) of lake waters changed from 136,200 to 250,400 mg/1]and the last value (calc.) was 1·025 (as TDS changed from 450,000 to 470,300 mg/1). Deuterium exchange with the atmosphere was apparently small except during late desiccation stages when the isotopic contrast became great. Eventually, atmospheric exchange, combined with decreasing α and lake size and increasing salinity, stopped further deuterium concentration in the lake. The maximum contrast between atmospheric vapor and lake deuterium contents was about 110%.

Geochimica et Cosmochimica Acta

Oxygen isotopes of some trondhjemites, siliceous gneisses, and associated mafic rocks

Analyses of oxygen isotopes in whole-rock samples of 58 Precambrian and Phanerozoic trondhjemites and siliceous gneisses and of 28 cogenetic mafic to intermediate rocks from North America, Fennoscandia, and southern Africa give the following results: 1. (1) 47 trondhjemites, tonalites, and mostly Archean acidic gneisses that apparently are not isotopically disturbed show an overage δ 15 O +7.3‰ "> +7.3‰ and a range of 5.2–8.9‰; 11 other samples are slightly to moderately disturbed and show higher values; and 2. (2) the mafic rocks show a wide range of δ-values, from about 0–9‰ but the undisturbed ones give an average δ 18 O of 5.2‰ "> 5.2‰ . The δ 18 O values of the trondhjemitic intrusives and siliceous gneisses of similar composition are lower than those of most granitic rocks and support models for derivation of these rocks from basaltic parents. This approach, however, cannot be used to determine if individual bodies formed by differentiation or by partial melting.

Precambrian Research

Meteoric water in magmas

Oxygen isotope analyses of sanidine phenocrysts from rhyolitic sequences in Nevada, Colorado, and the Yellowstone Plateau volcanic field show that δ 18 O decreased in these magmas as a function of time. This decrease in δ 18 O may have been caused by isotopic exchange between the magma and groundwater low in 18 O. For the Yellowstone Plateau rhyolites, 7000 cubic kilometers of magma could decrease in δ 18 O by 2 per mil in 600,000 years by reacting with water equivalent to 3 millimeters of precipitation per year, which is only 0.3 percent of the present annual precipitation in this region. The possibility of reaction between large magmatic bodies and meteoric water at liquidus temperatures has major implications in the possible differentiation history of the magma and in the generation of ore deposits.

Colorado, Nevada, Wyoming

Water and carbon in rusty lunar rock 66095

Lunar rock 66095 contains a hydrated iron oxide and has an unusual amount of water for a lunar rock (140 to 750 parts per million), 90 percent of which is released below 690°C. The δof water released at these low temperatures varies from -75 to -140 per mil relative to standard mean ocean water (SMOW). The small amount of water released between 690° and 1300°C has a δ of about -175 ±25 per mil SMOW. These δ values are not unusual for terrestrial water. The δ 18 O of water extracted from 110° to 400°C has a value of +5± I per mil SMOW, similar to the value for lunar silicates from rock 66095 and different from the value of -4 to -22 per mil found for samples of terrestrial rust including samples of rusted meteoritic iron. The amount of carbon varies from 11 to 59 parts per million with a δ 13 C from -20 to -30 per mil relative to Pee Dee belemnite. Only very small amounts of reduced species (such as hydrogen, carbon monoxide, and methane) were found, in contrast to the analyses of other lunar rocks. Although it is possible that most of the water in the iron oxide (goethite) may be terrestrial in origin or may have exchanged with terrestrial water during sample return and handling, evidence presented herein suggests that this did not happen and that some lunar water may have a δD that is indistinguishable from that of terrestrial water.

Science

Obsidian hydration dates glacial loading?

Three different groups of hydration rinds have been measured on thin sections of obsidian from Obsidian Cliff, Yellowstone National Park, Wyoming . The average thickness of the thickest (oldest) group of hydration rinds is 16.3 micrometers and can be related to the original emplacement of the flow 176,000 years ago (potassium-argon age). In addition to these original surfaces, most thin sections show cracks and surfaces which have average hydration rind thicknesses of 14.5 and 7.9 micrometers. These later two hydration rinds compare closely in thickness with those on obsidian pebbles in the Bull Lake and Pinedale terminal moraines in the West Yellowstone Basin, which are 14 to 15 and 7 to 8 micrometers thick, respectively. The later cracks are thought to have been formed by glacial loading during the Bull Lake and Pinedale glaciations, when an estimated 800 meters of ice covered the Obsidian Cliff flow.

Wyoming

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

Borax, gaylussite, nahcolite and trona were synthesized in aqueous solution at temperatures ranging from 8° to 35°C. Except for borax, deuterium was always depleted in these hydrated minerals relative to the solutions from which they were crystallized. In borax, no significant fractionation was found. The fractionation factor of D H "> DH for the trona-water system exhibited a marked temperature dependence. By combining the deuterium contents of trona and the solution from which trona was crystallized, the following thermometer scale was obtained: In ( D H ) trona ( D H )water = 1.420 × 10 4 T 2 + 23.56 T "> (DH) trona(DH)water =1.420 × 104T2+23.56T (1) An attempt to establish a geothermometer based on C 13 C 12 "> C13C12 fractionation between carbonate minerals and carbonate ions in aqueous solution was not successful.

Geochimica et Cosmochimica Acta

Deuterium content of snow as an index to winter climate in the Sierra Nevada area

The winter of 1968-69 produced two to three times the amount of precipitation in the Sierra Nevada area, California and Nevada, as the winter of 1969-70. The deuterium content in snow cores collected at the end of each winter at the same sites, which represents the total snowfall of each interval, shows a depletion in 1968-69 of approximately 20 per mil. The higher snowfall in 1968-69 and the depletion of deuterium can be explained by an uncommonly strong westward flow of cold air over and down the western slopes of the Sierras, which interacted with an eastward flow of moist Pacific air that overrode and mixed with the cold air; this resulted in precipitation that occurred in greater than normal amounts and at a lower than normal temperature. Pluvial periods of the Pleistocene may have had the same shift in air-mass trajectory as the wet 1968-69 year. Snow cores collected in the normal 1970-71 winter have deuterium concentrations that resemble those of the normal 1969-70 winter. Small and nonsystematic differences in samples from these two normal winters are due to variations in climatic character as well as to factors inherent in the sampling sites.

California, Nevada

Some investigations of the deposition of travertine from Hot Springs-I. The isotopic chemistry of a travertine-depositing spring

The isotopic compositions of the travertine and of the hot spring solutions were studied at Main Springs and New Highland Terrace in the Mammoth Hot Springs area of Yellowstone Park. The springs issue at 74°C and a pH of 6.65 and the carbon isotopic composition of the travertine depositing at the orifice is +2%.δC 13 (PDB). As the water travels out from the orifice, it cools and loses CO 2 . The travertine depositing at lower temperature is enriched in C 13 , reaching values of +4.8%. and the solution has a pH of 8.2 at 27°C. The δC 13 of the carbon species in solution is about −2.3%. at 74° and about +4.3 at 27°C. Therefore, the difference in δC 13 between the solid and solution is approximately 4%. at 74° and decreases to zero at about 20°C. These differences are shown to be due to kinetic (non-equilibrium) factors. The δO 18 contents of the travertine and water show that in most samples the carbonate oxygen is in equilibrium with the water O 18 at the temperatures of deposition. This is especially true for travertine depositing slowly and at temperatures above about 50°C. Calculations based on pH and alkalinity titrations of the hot spring waters in situ show that at the spring orifice the water is very high in free CO 2 , which is quickly lost in transit. The springs are supersaturated with respect to both aragonite and calcite during most of their travel in the open air. The carbon isotopic composition of the travertine is similar to that in the marine carbonates that are adjacent to the springs and that are the probable source of the calcium carbonate. The travertine from inactive prehistoric springs near Mammoth has similar δC 13 and O 18 to that from the active springs. Soda Butte, an inactive center 25 miles east of Mammoth, contains heavier carbon and oxygen than the springs near Mammoth.

Geochimica et Cosmochimica Acta

A new technique for pumping hydrogen gas

A system for pumping hydrogen gas without isotopic fractionation has been developed. The pump contains uranium metal, which when heated to about 80°C reacts with hydrogen to form UH 3 . The UH 3 is heated to above 500°C to decompose the hydride and regenerate the hydrogen.

Geochimica et Cosmochimica Acta

Water, hydrogen, deuterium, carbon, carbon-13, and oxygen-18 content of selected lunar material

The water content of the breccia is 150 to 455 ppm, with a δD from—580 to —870 per mil. Hydrogen gas content is 40 to 53 ppm with a δD of —830 to —970 per mil. The CO 2 is 290 to 418 ppm with δ 13 C = + 2.3 to + 5.1 per mil and δ 18 O = 14.2 to 19.1 per mil. Non-CO 2 carbon is 22 to 100 ppm, δ 13 C = —6.4 to —23.2 per mil. Lunar dust is 810 ppm H 2 O (D = 80 ppm) and 188 ppm total carbon(δ 13 C = —17.6 per mil). The 18 O analyses of whole rocks range from 5.8 to 6.2 per mil. The temperature of crystallization of type B rocks is 1100° to 1300°C, based on the oxygen isotope fractionation between coexisting plagioclase and ilmenite.

Science

Deuterium content of snow cores from Sierra Nevada area

The relative deuterium content was measured on 37 snow cores collected in April 1969 in the Sierra Nevada. The deuterium content varies inversely with altitude of collection (approximately 40 per mil per 1000 meters) but is unrelated to latitude. The altitude relationship is particularly well defined west of the crest of the range but is not well defined east of the crest. However, samples from east of the crest tend to be depleted by about 10 to 15 per mil relative to samples collected at the same elevation west of the crest. We propose that the deuterium content of snow cores, collected so as to include the total winter's precipitation, can be used as a climatic indicator to compare the climate of one winter with that of another.

California, Nevada

Deuterium: Natural variations used as a biological tracer

The suggestion is made that isotope tracing be carried out by monitoring the natural variations in deuterium concentrations. As an example, the natural variations in deuterium concentrations between food and water collected in Illinois and food and water collected in Colorado were used to determine the residence time of water in the blood and urine of rats. We observed not only a 51/2-day turnover time of water in the blood and urine, but also evidence for the influx of water vapor from the atmosphere through the lungs into the blood.

Science

Geochemistry and origin of formation waters in the western Canada sedimentary basin-I. Stable isotopes of hydrogen and oxygen

Stable isotopes of hydrogen and oxygen, together with chemical analyses, were determined for 20 surface waters, 8 shallow potable formation waters, and 79 formation waters from oil fields and gas fields. The observed isotope ratios can be explained by mixing of surface water and diagenetically modified sea water, accompanied by a process which enriches the heavy oxygen isotope. Mass balances for deuterium and total dissolved solids in the western Canada sedimentary basin demonstrate that the present distribution of deuterium in formation waters of the basin can be derived through mixing of the diagenetically modified sea water with not more than 2.9 times as much fresh water at the same latitude, and that the movement of fresh water through the basin has redistributed the dissolved solids of the modified sea water into the observed salinity variations. Statistical analysis of the isotope data indicates that although exchange of deuterium between water and hydrogen sulphide takes place within the basin, the effect is minimized because of an insignificant mass of hydrogen sulphide compared to the mass of formation water. Conversely, exchange of oxygen isotopes between water and carbonate minerals causes a major oxygen-18 enrichment of formation waters, depending on the relative masses of water and carbonate. Qualitative evidence confirms the isotopic fractionation of deuterium on passage of water through micropores in shales.

Alberta

Hydration rind dates rhyolite flows

Hydration of obsidian has been used to date rhyolite flows, containing obsidian or porphyritic glass, at Glass Mountain (Medicine Lake Highlands) and Mono Lake, California. The method is simple and rapid and can be used to date flows that erupted between 200 and approximately 200,000 years ago.

California

Hydration of natural glass and formation of perlite

The hydration rate of rhyolitic glass has been determined at temperatures ranging from 5° C to 100° C. The relationship between the depth of hydration, x, and time, t is x 2 = kt; k varies from 0.4 μ 2 /10 3 years at 5° C to 10 4 μ 2 /10 3 years at 100° C; k is independent of the water pressure from a few hundredths of a centimeter to 1 atm. water pressure. The activation energy of hydration is about 20 kcal/mole. The determined hydration rates are consistent with the observation that perlite commonly forms by the hydration of shattered rhyolitic glass, either during the late cooling of a deposit or after the deposit has cooled to a surficial temperature.

Geological Society of America Bulletin