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R.R. Seal

Publications and source records attributed to R.R. Seal.

34 records · Page 2Linked to original sources
USGS2002

Determination of melanterite-rozenite and chalcanthite-bonattite equilibria by humidity measurements at 0.1 MPa

Melanterite (FeSO 4 ·7H 2 O)-rozenite (FeSO 4 ·4H 2 O) and chalcanthite (CuSO 4 ·5H 2 O)-bonattite (CuSO 4 ·3H 2 O) equilibria were determined by humidity measurements at 0.1 MPa. Two methods were used; one is the gas-flow-cell method (between 21 and 98 °C), and the other is the humiditybuffer method (between 21 and 70 °C). The first method has a larger temperature uncertainty even though it is more efficient. With the aid of humidity buffers, which correspond to a series of saturated binary salt solutions, the second method yields reliable results as demonstrated by very tight reversals along each humidity buffer. These results are consistent with those obtained by the first method, and also with the solubility data reported in the literature. Thermodynamic analysis of these data yields values of 29.231 ± 0.025 and 22.593 ± 0.040 kJ/mol for standard Gibbs free energy of reaction at 298.15 K and 0.1 MPa for melanterite-rozenite and chalcanthite-bonattite equilibria, respectively. The methods used in this study hold great potential for unraveling the thermodynamic properties of sulfate salts involved in dehydration reactions at near ambient conditions.

American Mineralogist↗
USGS2001

Remnant colloform pyrite at the haile gold deposit, South Carolina: A textural key to genesis

Auriferous iron sulfide-bearing deposits of the Carolina slate belt have distinctive mineralogical and textural features-traits that provide a basis to construct models of ore deposition. Our identification of paragenetically early types of pyrite, especially remnant colloform, crustiform, and layered growth textures of pyrite containing electrum and pyrrhotite, establishes unequivocally that gold mineralization was coeval with deposition of host rocks and not solely related to Paleozoic tectonic events. Ore horizons at the Haile deposit, South Carolina, contain many remnants of early pyrite: (1) fine-grained cubic pyrite disseminated along bedding; (2) fine- grained spongy, rounded masses of pyrite that may envelop or drape over pyrite cubes; (3) fragments of botryoidally and crustiform layered pyrite, and (4) pyritic infilling of vesicles and pumice. Detailed mineral chemistry by petrography, microprobe, SEM, and EDS analysis of replaced pumice and colloform structures containing both arsenic compositional banding and electrum points to coeval deposition of gold and the volcanic host rocks and, thus, confirms a syngenetic origin for the gold deposits. Early pyrite textures are present in other major deposits of the Carolina slate belt, such as Ridgeway and Barite Hill, and these provide strong evidence for models whereby the sulfide ores formed prior to tectonism. The role of Paleozoic metamorphism was to remobilize and concentrate gold and other minerals in structurally prepared sites. Recognizing the significance of paragenetically early pyrite and gold textures can play an important role in distinguishing sulfide ores that form in volcanic and sedimentary environments from those formed solely by metamorphic processes. Exploration strategies applied to the Carolina slate belt and correlative rocks in the eastern United States in the Avalonian basement will benefit from using syngenetic models for gold mineralization.

Economic Geology↗
USGS2001

Selected data for sediment cores collected in Chesapeake Bay in 1996 and 1998

As part of a study of recent history of the Chesapeake Bay ecosystem, one- to eight- meter long sediment cores were obtained from the mesohaline section of the Chesapeake Bay between the mouths of the Potomac and Rhode Rivers. The sediments consist of three lithofacies: coarse-grained channel deposits, restricted-estuary sands and muds, and open-estuary muds. Water content, biogenic silica, magnetic susceptibility, trace metals, and nutrients (carbon, nitrogen, and their isotopes) were measured in the cores. Biogenic silica, trace-metal, and nutrient data provide a strong basis for discussing past primary productivity and water-column anoxia in the bay.

Cheapeake Bay↗
USGS1999

Evaluation of the sulfur isotopic composition and homogeneity of the Soufre de Lacq reference material

Sulfur isotopic analysis of the elemental sulfur reference material Soufre de Lacq, prepared as silver sulfide by chromous chloride reduction and as copper sulfide by sealed-tube synthesis, indicates that Soufre de Lacq is isotopically homogeneous across different size fractions to within analytical uncertainty (??0.15???). The sulfur isotopic composition of aliquots of Soufre de Lacq prepared by these two techniques are identical to within analytical uncertainty. The mean sulfur isotopic composition for Soufre de Lacq prepared as silver sulfide and copper sulfide (relative to VCDT) is +16.20 ?? 0.15??? (1??).

Chemical Geology↗
USGS1998

Geochemical and isotopic (Nd-Pb-Sr-O) variations bearing on the genesis of volcanic rocks from Vesuvius, Italy

Alkaline volcanism produced by Monte Somma-Vesuvius volcano includes explosive plinian and subplinian activity in addition to effusive lava flows. Pumice, scoria, and lava (150 samples) exhibit major- and trace-element gradients as a function of SiO2 (58.9-47.2 wt%) and MgO (0-7.8 wt%); Mg value are ???50. Internally gradational chemical groups or cycles are distinguished by age: (1) 25 000 to 14 000 yr B.P.; (2) 8000 yr B.P. to A.D. 79; and (3) A.D. 79 to 1944. A small number of lavas, dikes and scora were also analysed from the Somma formation (~ 35 000 to 25 000 yr B.P.). Within each group, contents of Na2O + K2O increas with decreasing MgO along distinct rocks. Nb/Y values are variable from 0.66 to 3.14 (at SiO2 ??? 50 wt%) generally in the range of alkaline and ultra-alkaline rocks. Variations in contents of some majro elements (e.g., P and Ti), and trace elements (e.g., Th, Nb, Ta, Zr, Hf, Pb, La, and Sc), as well as contrasting trends in ratios of various elements (e.g., Ta/Yb, Hf/U, Th/Ta, Th/Hf, Th/Yb, etc.) are also generally consistent with the group subdivisions. For example, Th/Hf increases from ??? 5 to ??? 10 with decreasing age for the Vesuvius system as a whole, yielding similar compositions in the least evolved rocks (low-silica, high-MgO, imcompatible element-poor) erupted at the end of each cycle. Internal variations within individual eruptions also systematically changed generally towards a common mafic composition at the end of each cycle, thus reflecting the dominanit volume in the magma chamber. At the start of a new eruptive cycle, the rocks are relatively enriched in incompatible elements; younger groups also contain higher abundances than other groups. N-MORB-normalized multielement diagrams exhibit selective enrichments of Sr, K, Rb, Th, and the light rare-earth elements; deep Nb and Ta negative anomalies commonly seen in rocks generated at orogenic margins are absent in the light rare-earth elements; deep Nb and Ta netgative anomalies commonly seen in rocks generated at orogenic margins are absent in our samples. Sr isotopic compositions are known to be variable within some of the units, in agreement with our data (87Sr/86Sr ~ 0.70699 to 0.70803) and with contributions from several isotopic components. Isotopic compositions for ??18O (7.3 to 10.2%), Pb for mineral separates and whole rocks (206Pb/204Pb ~ 18.947 to 19.178, 207Pb/204/Pb ~ 15.617 to 15.769, 208Pb/204Pb ~38.915 to 39.345), and Nd (143Nd ~ 0.51228 to 0.51251) also show variability. Oxygen isotope data show that pumices have higher ??18O values than cogenetic lavas, and that ??18O values and SiO2 are correlated. Radiogenic and stable isotope data plot within range of isotopic compositions for the Roman comagmatic province. Fractional crystallization cannot account for the radiogenic isotopic compositions of the Vesuvius magmas. We favor instead the combined effects of heterogeneous magma sources, together with isotopic exchange near the roof of the magma chamber. We suggest that metasomatized continental mantle lithosphere is the principal source of the magmas. This kind of enriched mantle was melted and reactivated in an area of continental extension (incipient rift setting) without direct reliance on contemporaneous subduction processes but possibly with input from mantle sources that resemble those that produce ocean island basalts.

Journal of Volcanology and Geothermal Research↗
USGS1998

Oxygen and hydrogen isotope systematics of Lake Baikal, Siberia: Implications for paleoclimate studies

We interpret oxygen and hydrogen isotope data for water samples from Lake Baikal, Siberia, its tributaries and other local rivers, and local precipitation in terms of the known water budget for the modem lake in order to gain insight into past limnological and climatic processes that influenced the lake. Lake Baikal is remarkably uniform in its isotopic composition (??18O = -15.8 ?? 0.2???; ??D = -123 ?? 2???) and lies slightly to the right of the global meteoric water line, which suggests significant evaporation. Water is supplied to the lake by over 300 rivers and streams. The oxygen isotope values (??18O) of the rivers in the Baikal catchment range from -13.4 to -21.2???. The hydrogen isotope values (??D) for the same area range from -103 to -156???. Both these ranges generally conform to the global meteoric water line. The weighted average isotopic composition of input to the lake (rivers plus precipitation) is -15.2??? for ??18O and -116??? for ??D, values higher than those of the modem lake. Therefore, the isotopic composition of the modem lake cannot be related to the modem input through simple evaporation. Instead, modeling of the isotopic mass balance of the lake suggests that inputs (precipitation and influx from rivers) and outputs (evaporation and outflow) are not at a steady-state equilibrium under current climate conditions. We found previous input to the lake had lower ??18O and ??D values than modem input, which reflects cooler climates in the past compared with modern conditions. Under constant climate conditions, steady-state conditions are not expected to be reached by the lake for at least 700 yr because of its large size and the long residence time of water in the lake.

Limnology and Oceanography↗
USGS1996

Heat capacity and entropy at the temperatures 5 K to 720 K and thermal expansion from the temperatures 298 K to 573 K of synthetic enargite (Cu3AsS4)

The heat capacity of synthetic Cu3AsS4 (enargite) was measured by quasi-adiabatic calorimetry from the temperatures 5 K to 355 K and by differential scanning calorimetry from T = 339 K to T = 720 K. Heat-capacity anomalies were observed at T = (58.5 ?? 0.5) K (??trsHom = 1.4??R??K; ??trsSom = 0.02??R) and at T = (66.5 ?? 0.5) K (??trsHom = 4.6??R??K; ??trsSom = 0.08??R), where R = 8.31451 J??K-1??mol-1. The causes of the anomalies are unknown. At T = 298.15 K, Cop,m and Som(T) are (190.4 ?? 0.2) J??K-1??mol-1 and (257.6 ?? 0.6) J??K-1??mol-1, respectively. The superambient heat capacities are described from T = 298.15 K to T = 944 K by the least-squares regression equation: Cop,m/(J??K-1??mol-1) = (196.7 ?? 1.2) + (0.0499 ?? 0.0016)??(T/K) -(1918 000 ?? 84 000)??(T/K)-2. The thermal expansion of synthetic enargite was measured from T = 298.15 K to T = 573 K by powder X-ray diffraction. The thermal expansion of the unit-cell volume (Z = 2) is described from T = 298.15 K to T = 573 K by the least-squares equation: V/pm3 = 106??(288.2 ?? 0.2) + 104??(1.49 ?? 0.04)??(T/K). ?? 1996 Academic Press Limited.

Journal of Chemical Thermodynamics↗
USGS1996

Hydrogen isotope systematics of phase separation in submarine hydrothermal systems: Experimental calibration and theoretical models

Hydrogen isotope fractionation factors were measured for coexisting brines and vapors formed by phase separation of NaCl/H2O fluids at temperatures ranging from 399-450??C and pressures from 277-397 bars. It was found that brines are depleted in D compared to coexisting vapors at all conditions studied. The magnitude of hydrogen isotope fractionation is dependent on the relative amounts of Cl in the two phases and can be empirically correlated to pressure using the following relationship: 1000 ln ??(vap-brine) = 2.54(??0.83) + 2.87(??0.69) x log (??P), where ??(vap-brine) is the fractionation factor and ??P is a pressure term representing distance from the critical curve in the NaCl/H2O system. The effect of phase separation on hydrogen isotope distribution in subseafloor hydrothermal systems depends on a number of factors, including whether phase separation is induced by heating at depth or by decompression of hydrothermal fluids ascending to the seafloor. Phase separation in most subseafloor systems appears to be a simple process driven by heating of seawater to conditions within the two-phase region, followed by segregation and entrainment of brine or vapor into a seawater dominated system. Resulting vent fluids exhibit large ranges in Cl concentration with no measurable effect on ??D. Possible exceptions to this include hydrothermal fluids venting at Axial and 9??N on the East Pacific Rise. High ??D values of low Cl fluids venting at Axial are consistent with phase separation taking place at relatively shallow levels in the oceanic crust while negative ??D values in some low Cl fluids venting at 9??N suggest involvement of a magmatic fluid component or phase separation of D-depleted brines derived during previous hydrothermal activity.

Geochimica et Cosmochimica Acta↗
USGS1993

Stable isotope study of fluid inclusions in fluorite from Idaho: Implications for continental climates during the Eocene

Isotopic studies of fluid inclusions from meteoric water-dominated epithermal ore deposits offer a unique opportunity to study paleoclimates because the fluids can provide direct samples of ancient waters. The oxygen and hydrogen isotope compositions of meteoric waters vary because of changes in climatic variables such as mean annual temperature of precipitation, relative humidity, origin and history of air masses, and the isotope composition of the oceans. Inclusion fluids found in fluorite (CaF 2 ) are especially useful because their host is devoid of oxygen or hydrogen, thus precluding postentrapment isotope exchange. Fluorite-hosted fluid inclusions from the Eocene (51-50 Ma) epithermal deposits of the Bayhorse mining district, northeastern Idaho, have low salinities, most less than 0.6 equivalent wt% NaCl, and low to moderate homogenization temperatures (98 to 146 °C), indicating meteoric origins for the fluids. Oxygen and hydrogen isotope data on inclusion fluids are almost identical to those of modern meteoric waters in the area. The equivalence of the isotope composition of the Eocene inclusion fluids and modern meteoric waters indicates that the Eocene climatic conditions were similar to those today. This conclusion supports the climate modeling of Sloan and Barron, who suggested that the climates of continental interiors do not reflect the magnitude of warming preserved by the deep-ocean paleoclimate record during the Eocene.

Geology↗
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↗