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R. O. Rye

Publications and source records attributed to R. O. Rye.

At least 55 records · Page 3Linked to original sources
USGS1992

Stable isotope study of water-rock interaction and ore formation, Bayhorse base and precious metal district, Idaho

The Bayhorse base and precious metal district is situated east of the Idaho batholith in south-central Idaho. The ores occur near the Nevada Mountain granitic stock as veins cutting the lower Paleozoic Ramshorn Slate and the Garden Creek Phyllite, and as fillings around breccia fragments within the Bayhorse Dolomite. The veins are dominated by siderite and tetrahedrite, with lesser quartz and galena, whereas the breccia ores dominantly comprise only quartz and galena. Mineralization and intrusive activity were contemporaneous during Cretaceous time. Fluid inclusion and stable isotope data indicate that mineralization formed from hot (ca. 375 degrees -225 degrees C), CO 2 -rich (< or =8.3+ or -1.4 mole %) brines (5-20 wt % NaCl equiv) at confining pressures between 1.1 and 1.7 kbars. Fluid cooling and the resulting CO 2 effervescence were the most important causes of ore deposition.Whole-rock delta 18 O and delta D values from the Garden Creek Phyllite define an isotopically depleted zone (60 km 2 ) around the Nevada Mountain stock and are the result of high-temperature interactions with ancient meteoric waters at water/rock ratios (mass fractions) ranging from 0.002 to 0.09. The delta 18 O (sub H 2 O) and delta D (sub H 2 O) values of the ore fluids ranged from 11.2 to 3.9 per rail and from -55 to -146 per mil, respectively. Comparison of the ore fluid delta 18 O (sub H 2 O) and delta D (sub H 2 O) values with hypothetical waters equilibrated with the Garden Creek Phyllite intricates that the hydrothermal fluids must have also interacted with the basal dolomite of Bayhorse Creek, which underlies the phyllite. Early delta 13 C (sub CO 2 ) values calculated in equilibrium with siderite ranged from -9.1 to -7.4 per mil, whereas later delta 13 C (sub CO 2 ) values obtained from quartz-hosted fluid inclusion extracts range from -4.0 to -1.8 per mil. The delta 13 C (sub CO 2 ) values for the hydrothermal fluids thus also record a transition from early water/rock interactions that were dominated by the Garden Creek Phyllite (organic matter delta 13 C = -23.6 to -20.9ppm) to later interactions that were influenced significantly by the basal dolomite of Bayhorse Creek (delta 13 C = -2.3 to -2.2ppm). The delta 34 S values of main-stage hydrothermal sulfides range from 3.0 to 28.3 per mil and display a distinct mode at approximately 10 per mil. The range of values may be interpreted as either a heterogeneous sedimentary source or mixed sedimentary-magmatic sources. On the basis of mass balance considerations, it is likely that all of the fluid salinity and the dissolved metals were derived from the Garden Creek Phyllite. The paragenetic sequence developed in the ores appears to be related to: (1) processes at the site of deposition, most notably cooling and CO 2 effervescence, and (2) water-rock interactions within the Garden Creek Phyllite in the 60-km 2 isotopically altered area surrounding the Nevada Mountain stock.

Economic Geology↗
USGS1988

Stable isotope geochemistry of sphalerite and other mineral matter in coal beds of the Illinois and Forest City basins

Cleat and clastic dikes of Middle Pennsylvanian-age coal beds of the Illinois and Forest City basins of Illinois, Iowa, Missouri, and Kansas locally contain appreciable amounts of sphalerite within a kaolinite-pyrite-sphalerite (+ or - pyrite)-calcite paragenetic sequence. The sphalerite and associated minerals are of interest as a partial record of the history of fluids in the sedimentary basin and as possible indicators of Mississippi Valley-type mineralization. Moreover, zinc from the sphalerite may represent an exploitable by-product of coal mining and combustion.Pyrite is abundant in these coals both as fine-grained disseminated framboids that formed during early diagenesis and as coarser grained cleat fillings, etc., that formed much later. The delta 34 S values of this later pyrite, the sphalerite, and the coal organic matter range from -12 to 19 per mil. Within individual samples, however, pyrite, sphalerite, and organic matter sulfur delta 34 S values are nearly identical. This similarity strongly suggests related origins. The delta 34 S values of pyrite, sphalerite, and organic matter from coals of the Illinois basin and the central and southern Forest City basin range from -12 to 0 per mil. This range is not unique to the sphalerite-bearing coals; pyrite and organic matter from sphalerite-free high sulfur coals have similar delta 34 S values (Price and Shieh, 1979). We believe that sulfur produced by the breakdown of organosulfur compounds in the coal is incorporated into the epigenetic sulfides. In the northern Forest City basin, however, many samples have delta 34 S values between 8 and 19 per mil. These are similar to the delta 34 S values of sphalerite and pyrite from the Upper Mississippi Valley Zn-Pb district which lies northeast of the Forest City basin and north of the Illinois basin. This similarity suggests input from a Mississippi Valley-type hydrothermal system.Cleat kaolinite has delta D values of -36 to -24 per mil and delta 18 O values of 19.2 to 20.2 per mil. Assuming that clearing postdated the lignite rank of coalification implies that kaolinite was deposited between 40 degrees and 100 degrees C. At the lower temperatures, the kaolinite fluid would have had an isotopic composition similar to seawater; at the higher temperatures, it would have had a composition similar to the sphalerite-depositing fluid. Sphalerite was deposited from a fluid that was chemically and isotopically similar to the fluids responsible for the main-stage ores of the Upper Mississippi Valley Zn-Pb district (75 degrees -113 degrees C, approximately 21 equiv wt % NaCl, delta D = -65 to -3ppm, and delta 18 O = -0.9-9.9ppm). The isotopic compositions (delta 13 C = -12.4 to -2.7ppm and delta 18 O = 21.1-25.8ppm) and paragenetic positions of the cleat calcite samples are similar to those of the late-stage calcite of the Upper Mississippi Valley Zn-Pb and Illinois-Kentucky fluorspar districts. Calcite inclusion fluids had delta D (sub H 2 O) values of -80 and -58 per mil, implying a meteoric water source. At probable temperatures of 15 degrees to 75 degrees C, this calcite formed from fluids having calculated delta 18 O (sub H 2 O) values of -9 to 1 per mil, implying slight to moderate exchange with sedimentary rocks. The diagenetic-epigenetic history of fluids recorded by the cleat minerals probably began with a slightly evolved seawater, followed by a metal-bearing deep basin brine, and concluded with a cooler, slightly evolved, meteoric-water fluid.

Economic Geology↗
USGS1985

PRE-ORE POTASSIUM METASOMATISM, CREEDE MINING DISTRICT, COLORADO.

Rhyolitic welded-tuff wallrocks of the epithermal base and precious metal veins of the Creede district were pervasively altered by the addition of more than two billion metric tons of potassium some 1. 5-2 million years before mineralization. Sodium, calcium and magnesium were strongly depleted, yielding a nearly binary quartz plus potassium feldspar assemblage containing as much as 13 weight percent K//2O. This large-scale metasomatism, originally noted by Steven and Rattle (1965), took place progressively by initial alteration of plagioclase phenocrysts to orthoclase or microcline followed by alteration of the groundmass feldspar to orthoclase and gradual change of the sanidine phenocrysts to more Or-rich compositions. Oxygen isotope and chemical studies show that the metasomatism resulted from the interaction of the tuffs with deeply circulating heated ground water and suggest that the potassium metasomatism of rhyolitic rocks is the facies equivalent of propylitization of volcanic rocks of more basic composition.

Conference Paper↗
USGS1984

The Balmat-Edwards zinc-lead deposits; synsedimentary ore from Mississippi Valley-type fluids

Reconstruction of some aspects of the initial environment of ore deposition through detailed S, C, and O isotope studies of the Fowler orebody, and through reconnaissance trace element and S isotope studies of sphalerite concentrates and composite samples of ore from 22 orebodies; and (2) evaluation of the effects of high-grade metamorphism on the stable isotope geochemistry of both the ore and gangue minerals of a massive sulfide orebody. The delta 34 S values of pyrite, sphalerite, and galena in the Fowler orebody range from 11.5 to 17.5 per mil; anhydrite associated with ore ranges from 25.6 to 27.0 per mil. Average equilibration temperatures calculated from the delta 34 S differences between coexisting sulfur-bearing phases are 388 degrees C for pyrite-sphalerite, 338 degrees C for sphalerite-galena, 329 degrees C for pyrite-galena, and 602 degrees C for anhydrite-pyrite; all pairs display narrow temperature distributions. The delta 13 C and delta 18 O values of carbonates from the Fowler orebody range from -1.6 to 1.4 per mil and from 24.8 to 27.0 per mil, respectively; quartz delta 18 O values range from 23.0 to 27.0 per mil. The delta 34 S values of sphalerite concentrated from composite samples of the orebodies range from 12.7 to 14.7 per mil. This narrow range contrasts sharply with the wide variability of associated evaporitic anhydrite lenses, which range from 8 to 28 per mil. A stratigraphic increase in the delta 34 S value of the evaporitic anhydrite at Balmat, and large sulfide iron-formation occurrences near Balmat, imply that bacterial sulfate reduction occurred on an unusually large scale during Balmat sedimentation. The presence of such an increase in a sedimentary section may constitute a valuable exploration guide.

Economic Geology↗
USGS1984

Origins and exploration significance of replacement and vein-type alunite deposits in the Marysvale volcanic field, west central Utah

Alunite deposits formed 23 m.y. ago in near-surface, highly oxidizing conditions at the tops of hydrothermal plumes that were spaced at 3- to 4-km intervals around a monzonite stock. The delta 34 S values of 11.5 to 15.4 per mil for replacement alunite along with geologic constraints indicate that sulfate sulfur was derived from underlying Mesozoic evaporites. The delta 34 S values of -15.3 to +5.1 per mil of underlying pyrite, however, indicate that reduced sulfur, necessary to produce low pH during oxidation, either was produced by partial reduction of the evaporite sulfate or came from another source. Vein-type alunite deposits formed 14 m.y. ago as open-space fillings in extension fractures above a concealed stock. Crystals of alunite grew inward from the walls, forming veins of nearly pure alunite as much as 20 m thick. The delta 34 S values near zero per mil indicate that the vein-type alunite sulfur probably had a magmatic source, and it appears that the sulfur may have been present as SO 2 shortly after degassing from the magma. The probable magmatic origin for sulfur in the 14-m.y.-old vein-type alunite and its deposition from vapor-rich fluids, as well as the probable magmatic origin for sulfur in the surrounding base and precious metal deposits, suggest that the underlying stock may host porphyry-type deposits.

Economic Geology↗
USGS1984

Sulfur and oxygen isotopic systematics of the 1982 eruptions of El Chichón Volcano, Chiapas, Mexico

Thermometers based on sulfur and oxygen isotopic compositions of anhydrite, pyrrhotite, titanomagnetite, and plagioclase crystals from fresh pumices of the 1982 eruptions of El Chich&oacute;n Volcano indicate a pre-eruption temperature of 810 &plusmn; 40&deg;C, confirming textural evidence that the anhydrite precipitated directly from the melt. The isotopic composition of sulfate leached from fresh ashfall samples shows it to be a mixture of anhydrite microphenocrysts and adsorbed sulfate derived from oxidized sulfur (SO 2 ) in the eruption plume. The leachate data show no evidence for rapid oxidation of significant amounts of H 2 S in the eruption cloud even though the fugacity ratio of H 2 S/SO 2 in the gas phase of the magma was >400. This may indicate kinetic inhibition of H 2 S to SO 2 conversion in the eruption cloud. Prior to eruption, the magma contained an estimated 2.6 wt. % sulfur (as SO 3 ). The estimated &delta; 34 S of the bulk magma is 5.8&permil;. Such a high value may reflect assimilation of 34 S-enriched evaporites or the prior loss of 34 S-depleted H 2 S to a fluid or gas phase during formation of a small prophyry-type hydrothermal system or ore deposit. In either case, the original magma must have been very sulfur rich. It is likely that the initial high sulfur content of the magma and at least some of its 34 S enrichment reflects involvement of subducted volcanogenic massive sulfides deposits during Benioff-zone partial melting. Isotopic data on mineralized, accidental lithic fragments support the possible development of a porphyry-type system at El Chich&oacute;n.

Journal of Volcanology and Geothermal Research↗
USGS1983

Role of fluid mixing and fault-related sulfide in the origin of the Ray Point uranium district, south Texas

The Lamprecht and Felder deposits are roll-type deposits hosted by the Miocene Oakville Sandstone. Four distinct stages of FeS 2 mineral formation are recognized: (1) a generation of isotopically light (delta 34 S < -20 per mil) preore pyrite, (2) a generation of isotopically light (delta 34 S < -20 per mil) marcasite that formed mostly before, but also during ore deposition, (3) a postore generation of isotopically heavy pyrite (delta 34 S > 0 per mil), and (4) a yet later generation of marcasite with isotopically light sulfur close to the values of stages 1 and 2. Complex zone of mixing between saline brines migrating up the fault from depth and oxygenated meteoric water recharging at the outcrop. Bacterial activity.

Economic Geology↗
USGS1979

Environment of ore deposition in the Creede mining district, San Juan Mountains, Colorado; Part IV, source of fluids, from oxygen, hydrogen, and carbon isotope studies

The hydrogen isotopic composition of fluids responsible for formation of the near-surface silver-base metal vein deposits at Creede was measured by direct analysis of inclusion fluids in sphalerite, quartz, and rhodochrosite and was estimated from analyses of illite and chlorite. The oxygen isotopic composition was determined directly on inclusion fluids in sphalerite and was estimated from analyses of quartz, illite, rhodochrosite, siderite, and adularia. The carbon isotopic composition was estimated from analyses of rhodochrosite and siderite. The ranges in isotopic composition for water and CO 2 in the fluids associated with the formation of each of the minerals is given below (number of determinations given in parentheses):Mineral delta D (sub H 2 ) O ppm delta 18 O (sub H 2 ) O ppm delta 13 C (sub CO 2 ) ppmSphalerite -81 to -54 (4) -10.1 to -4.5 (4)Quartz -97 to -86 (4) -5.9 to 1.8 (18)Illite -62 to -50 (8) -1.6 to 1.2(7)Chlorite -64 to -55 (10) -2.2 to 0.8 (10)Adularia 4.2 (1)Rhodochrosite -82 to -78 (2) 4.2 to 9.4 (9) -5.7 to -4.2 (9)Siderite 4.9 to 9.9 (6) -6.9 to -2.7 (6)The delta D (sub H 2 ) O and delta 18 O (sub H 2 ) O values of fluids associated with the formation of sphalerite, quartz, illite/chlorite, and carbonate minerals differ substantially from one another, and these differences appear to have been maintained throughout the depositional history, regardless of the positions of the minerals in the paragenetic sequence.The data suggest that waters from three coexisting reservoirs fed the vein system alternately and episodically during vein formation, and apparently there was little mixing of the fluids from the different reservoirs. The hydrogen, oxygen, and carbon isotope data suggest that the carbonate waters were deep seated, probably dominantly magmatic, in origin. The sphalerite and illite/chlorite waters must have been dominantly meteoric in origin and substantially oxygen shifted by exchange with the volcanic country rocks. The quartz waters were also oxygen shifted meteoric waters but were some 40 per mil lower in deuterium content than the sphalerite and illite/chlorite waters.We propose that the quartz fluids entered the vein system from reservoirs beneath the mountainous areas to the north in the vicinity of the present Continental Divide, but that the sphalerite and illite/chlorite fluids entered the vein system from a topographically low area to the south along the structural moat of the Creede caldera. The difference in delta D between the two meteoric waters may reflect differences in altitude of the recharge areas for the two reservoirs or may be clue to isotopic evolution of the closed-basin lake and interstitial waters in the moat surrounding the Creede caldera.

Colorado↗
USGS1978

Stable isotope studies of bedded barite at East Northumberland Canyon in Toquima Range, central Nevada

Several beds of barite occur in the Slaven Chert at East Northumberland Canyon in the Toquima Range of central Nevada. Most of the barite is internally laminated but shows massive weathering. However, rosette, disseminated, conglomeratic, and concretionary varieties also occur. New fossil evidence from conodonts and brachiopods indicates a Late Devonian age for the Slaven Chert at East Northumberland Canyon. Preliminary δ 34 S values of most disseminated and massive-laminated barite within the Slaven Chert average about 25 permil; these are within the range of values that is typical of sulfate from Late Devonian seawater and are distinctly different from δ 34 S values of most crosscutting hydrothermal barite veins in the area. Primary δ 34 S values of the bedded barite appear to be retained during recrystallization and hydrothermal alteration, suggesting that δ 34 S data of bedded barites could be developed into a useful stratigraphic tool. The δ 34 S values of rosette and concrectionary barites range from 29.1 to 56.3 permil and indicate that these varieties of barite formed in restricted microenvironments where extensive bacterial reduction of seawater sulfate occurred. The δ 18 O data on cherts associated with the barite beds and δ 14 C and δ 18 O data on carbonate beds within the Slaven Chert indicate that the depositional environment at tames had restricted communication with normal seawater of the open ocean.

Nevada↗
USGS1976

Carbon, hydrogen, and oxygen isotope studies of the regional metamorphic complex at Naxos, Greece

At Naxos, Greece, a migmatite dome is surrounded by schists and marbles of decreasing metamorphic grade. Sillimanite, kyanite, biotite, chlorite, and glaucophane zones are recognized at successively greater distances from the migmatite dome. Quartz-muscovite and quartz-biotite oxygen isotope and mineralogie temperatures range from 350 to 700°C. The metamorphic complex can be divided into multiple schist-rich (including migmatites) and marblerich zones. The δ 18 O values of silicate minerals in migmatite and schist units and quartz segregations in the schist-rich zones decrease with increase in metamorphic grades. The calculated δ 18 O H2O values of the metamorphic fluids in the schist-rich zones decrease from about 15‰ in the lower grades to an average of about 8.5‰ in the migmatite. The δD values of OH-minerals (muscovite, biotite, chlorite, and glaucophane) in the schist-rich zones also decrease with increase in grade. The calculated δD H2O values for the metamorphic fluid decrease from −5‰ in the glaucophane zone to an average of about −70‰ in the migmatite. The δD values of water in fluid inclusions in quartz segregations in the higher grade rocks are consistent with this trend. Theδ 18 O values of silicate minerals and quartz segregations in marble-rich zones are usually very large and were controlled by exchange with the adjacent marbles. The δD values of the OH minerals in some marble-rich zones may reflect the value of water contained in the rocks prior to metamorphism. Detailed data on 20 marble units show systematic variations of δ 18 O values which depend upon metamorphic grade. Below the 540°C isograd very steep δ 18 O gradients at the margins and large δ 18 O values in the interior of the marbles indicate that oxygen isotope exchange with the adjacent schist units was usually limited to the margins of the marbles with more exchange occurring in the stratigraphic bottom than in the top margins. Above the 540°C isograd lower δ 18 O values occur in the interior of the marble units reflecting a greater degree of recrystallization and the occurrence of Ca-Mg-silicates. Almost all the δ 13 C values of the marbles are in the range of unaltered marine limestones. Nevertheless, the δ 13 C values of most marble units show a general correlation with δ 18 O values. The CO 2 H 2 O "> CO 2 H 2 O mole ratio of fluid inclusions in quartz segregations range from 0.01 to 2. Theδ 13 C values of the CO 2 range from −8.0 to 3.6‰ and indicate that at some localities CO 2 in the metamorphic fluid was not in carbon isotopic equilibrium with the marbles.

Geochimica et Cosmochimica Acta↗
USGS1974

Stable isotope and lead isotope study of the Cortez, Nevada, gold deposit and surrounding area

Isotope studies of sulfur, carbon, hydrogen, oxygen, and lead were carried out to clarify the age and origin of the Cortex gold deposit and the surrounding mineralized area. The hydrogen isotope data indicate that meteoric water was the dominant component of the ore-forming fluids at Cortez. The hydrogen isotope data support geologic evidence for a Tertiary age for the deposit. The oxidation of the ore probably occurred during the deposition of postore calcite and was caused by waters whose oxygen isotopic composition was distinctly different from that of the ore fluids. The carbon isotope data suggest that the only carbon present in the ore fluids was derived from solution of the host rock. The lead and sulfur data are consistent with a possible sedimentary derivation for the gold in the ore. Lead and sulfur isotope distributions indicate that much of the galena mineralization in the area occurred during the Jurassic.

Nevada↗