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P. J. Aruscavage

Publications and source records attributed to P. J. Aruscavage.

At least 19 recordsLinked to original sources
USGS2012

Uniformity and diversity in the composition of mineralizing fluids from hydrothermal vents on the southern Juan de Fuca Ridge

Abundances of Li, Na, K, Rb, Ca, Sr, Ba, Mn, Fe, Zn, and Si have been determined in fluid samples from seven vents located in three areas on the southern Juan de Fuca Ridge. The hydrothermal component estimated from the Mg contents of the samples ranges from 7% to 76%. Concentrations of Fe and Si, among other elements, in acid-stabilized solutions appear to be generally representative of the parental hydrothermal fluids, but some Zn determinations and most Ba values appear to be too low. Thermodynamic calculations indicate that the acidified samples remain supersaturated with respect to silica, barite, and pyrite; unacidified samples are supersaturated, in addition, with respect to ZnS, FeS, and many silicate phases. Within the constraints of limited sampling there appear to be differences in fluid compositions both within and between the three vent areas. Some uniform differences in the elemental abundances predicted for hydrothermal end-member fluids might be due to inmixing of fresh seawater at depth in the hydrothermal system. The Juan de Fuca hydrothermal fluids contain more Fe but otherwise have relative elemental abundances fairly similar to those in 13°N (East Pacific Rise) fluids, albeit at higher levels. In contrast, fluids from 21°N (East Pacific Rise) and Galapagos have lower K/Rb and much lower Sr and Na abundances; these compositional features probably result from interaction of these fluids with a different mineral assemblage, possibly more mature greenstone.

Journal of Geophysical Research Solid Earth↗
USGS2002

Combustion and leaching behavior of elements in the argonne premium coal samples

Eight Argonne Premium Coal samples and two other coal samples were used to observe the effects of combustion and leaching on 30 elements. The results were used to infer the modes of occurrence of these elements. Instrumental neutron activation analysis indicates that the effects of combustion and leaching on many elements varied markedly among the samples. As much as 90% of the selenium and bromine is volatilized from the bituminous coal samples, but substantially less is volatilized from the low-rank coals. We interpret the combustion and leaching behavior of these elements to indicate that they are associated with the organic fraction. Sodium, although nonvolatile, is ion-exchangeable in most samples, particularly in the low-rank coal samples where it is likely to be associated with the organic constituents. Potassium is primarily in an ion-exchangeable form in the Wypdak coal but is in HF-soluble phases (probably silicates) in most other samples. Cesium is in an unidentified HNO3-soluble phase in most samples. Virtually all the strontium and barium in the low-rank coal samples is removed by NH4OAc followed by HCl, indicating that these elements probably occur in both organic and inorganic phases. Most tungsten and tantalum are in insoluble phases, perhaps as oxides or in organic association. Hafnium is generally insoluble, but as much as 65% is HF soluble, perhaps due to the presence of very fine grained or metamict zircon. We interpret the leaching behavior of uranium to indicate its occurrence in chelates and its association with silicates and with zircon. Most of the rare-earth elements (REE) and thorium appear to be associated with phosphates. Differences in textural relationships may account for some of the differences in leaching behavior of the REE among samples. Zinc occurs predominantly in sphalerite. Either the remaining elements occur in several different modes of occurrence (scandium, iron), or the leaching data are equivocal (arsenic, antimony, chromium, cobalt, and nickel). The results of these combustion and leaching experiments indicate that some previously held assumptions concerning modes of occurrence of elements in coal should be reconsidered.

Energy & Fuels↗
USGS1990

Fractionation of palladium and platinum in a Mesozoic diabase sheet, Gettysburg basin, Pennsyvania: Implications for mineral exploration

The York Haven diabase sheet displays clear-cut evidence of fractionation of Pd and Pt during differentiation of a high-Ti (about 1.1%) quartz-normative tholeiitic magma (York Haven type). At York Haven the sheet is about 750 m thick. It is characterized by abundant cumulus MgO-rich orthopyroxene (bronzite), and is markedly depleted in incompatible elements relative to the chilled margins. In contrast, at Reesers Summit, 16 km to the northwest, the sheet is about 500 m thick and consists of evolved rocks that have contents of incompatible elements two to three times greater than in the enclosing chilled margins. These evolved rocks represent complementary fractions to the cumulate rocks at York Haven. Mineralogic, petrologic and geochemical variations suggest considerable lateral migration and fractionation of the initial magma. Chilled margins of both sections have essentially the same Pd and Pt contents (10 ppb each) and similar Pd to Pt ratios (1.2). During differentiation, the cumulate rocks at York Haven were enriched in Pt and depleted in Pd, whereas at Reesers Summit, the low-MgO diabase and ferrogabbro zone were enriched in Pd relative to Pt. Anomalously high contents of Pd (to 165 ppb), Au (to 54 ppb), and Te (to 26 ppb) were found in an iron- (to 18%) and chlorine- (to 0.44%) rich ferrogabbro at Reesers Summit, suggesting possible late or post-magmatic enrichment of precious metals. Field relations, geochemical and petrographic data provide guides for further exploration for Pd and Pt in differentiated high-Ti quartz-normative diabase sheets. Based on present information, the most favorable sites for economic deposits are late-stage differentiates enriched in Fe and Cl. ?? 1990.

Pennsylvania↗
USGS1987

Composition of fluid inclusions in Permian salt beds, Palo Duro Basin, Texas, U.S.A.

Several methods have been developed and used to extract and chemically analyze the two major types of fluid inclusions in bedded salt from the Palo Duro Basin, Texas. Data on the ratio K: Ca: Mg were obtained on a few of the clouds of tiny inclusions in "chevron" salt, representing the brines from which the salt originally crystallized. Much more complete quantitative data (Na, K, Ca, Mg, Sr, Cl, SO4 and Br) were obtained on ??? 120 individual "large" (mostly ???500 ??m on an edge, i.e., ??? ??? 1.6 ?? 10-4 g) inclusions in recrystallized salt. These latter fluids have a wide range of compositions, even in a given piece of core, indicating that fluids of grossly different composition were present in these salt beds during the several (?) stages of recrystallization. The analytical results indicating very large inter-and intra-sample chemical variation verify the conclusion reached earlier, from petrography and microthermometry, that the inclusion fluids in salt and their solutes are generally polygenetic. The diversity in composition stems from the combination of a variety of sources for the fluids (Permian sea, meteoric, and groundwater, as well as later migrating ground-, formation, or meteoric waters of unknown age), and a variety of subsequent geochemical processes of dissolution, precipitation and rock-water interaction. The compositional data are frequently ambiguous but do provide constraints and may eventually yield a coherent history of the events that produced these beds. Such an understanding of the past history of the evaporite sequence of the Palo Duro Basin should help in predicting the future role of the fluids in the salt if a nuclear waste repository is sited there. ?? 1987.

Chemical Geology↗
USGS1984

Ferromanganese crust resources in the Pacific and Atlantic Oceans

Ferromanganese crusts on raised areas of the ocean floor have joined abyssal manganese nodules and hydrothermal sulfides as potential marine resources. Significant volumes of cobalt-rich (about 1% Co) crusts have been identified to date within the US Exclusive Economic Zone (EEZ) in the Central Pacific: in the NW Hawaiian Ridge and Seamount region and in the seamounts in the Johnston Island and Palmyra Island regions. Large volumes of lower grade crusts, slabs, and nodules are also present in shallow ( greater than 1000 m) waters on the Blake plateau, off Florida-South Carolina in the Atlantic Ocean. Data on ferromanganese crusts have been increased by recent German and USGS cruises, but are still sparse, and other regions having crust potential are under current investigation. The authors discuss economic potentials for cobalt-rich crusts in the Central Pacific and Western North Atlantic oceans, with special reference to US EEZ areas. Additional research is needed before more quantitative resource estimates can be made.

Conference Paper↗
USGS1984

Ferromanganese micronodules from the surficial sediments of Georges Bank

Ferromanganese micronodules have been found on Georges Bank, off the U.S. northeast coast, distributed throughout the surficial sediments within an area about 125 km long and at least 12 km wide. These coarse, sand-sized concretions have precipitated from metal-rich interstitial waters and contain many of the textural and structural features common to other neritic nodules. Most of the nodules have accreted around detrital grains, and X-ray powder diffraction analyses indicate the presence of geothite and vernadite (  -MnO 2 ) in the ferromanganese layers. Chemical analyses of the micronodules, when compared with similar data on deep-sea manganese nodules, reveal lower Mn/Fe ratios, significantly higher concentrations of V and As, comparable values of Mo, and an order of magnitude less of Co, Ni, Ce and most other metals.

Georges Bank↗
USGS1984

The Georges Bank monitoring program 1983: Analysis of trace metals in bottom sediments

From July 1981, when drilling began on Georges Bank, to May 1982, the concentration of barium, a major element in drilling mud, has increased by a factor of 3.5 in bulk sediments 200 m from the drill site in block 410 and by a factor of 2.3 at the drill site in block 312. The postdrilling barium concentrations are within the range of predriiling concentrations measured at other locations on Georges Bank. We estimate that no more than 21 percent of the barite (principal barium-bearing mineral) discharged during drilling remains within 6 km of the drill site in block 312. No drilling-related changes in the concentration of chromium or other metals have been observed in bulk sediments from blocks 410 or 312. The chemical signal of drilling mud in surficial sediments has been enhanced by separating and analyzing the sediment fraction finer than 60 ?m. Barium concentrations in the fine fraction have increased by factors of 36 and 22 at the drill sites in blocks 410 and 312, respectively. At the drill site in block 410, aluminum, chromium, copper, and mercury concentrations in this fraction temporarily increased by approximately a factor of 2 and then decreased to background. The concentrations of aluminum, barium, cadmium, chromium, copper, iron, lead, manganese, mercury, nickel, organic carbon, vanadium, and zinc in surface sediments of Georges Bank both before and after drilling are low compared to concentrations in average crustal rocks and are characteristic of unpolluted, coarse-grained sediments as found in other Continental Shelf areas.

Georges Bank↗
USGS1983

Platinum-group elements in rocks from the voikar-syninsky ophiolite complex, Polar Urals, U.S.S.R.

Analyses of platinum-group elements (PGE) in rocks collected from the Voikar-Syninsky ophiolite in the Polar Urals suggest that the distribution and geochemistry of PGE in this Paleozoic ophiolite are similar to those in Mesozoic ophiolites from elsewhere. Chondrite-normalized PGE patterns for chromitite, the tectonite unit, and ultramafic and mafic cumulate unit have negative slopes. These results are similar to those found for chromitites from other ophiolites; stratiform chromities show positive slopes. If the magmas that form both types of chromitite originate from similar mantle source material with respect to PGE content, the processes involved must be quite different. However, the distinct chondrite-normalized PGE patterns may reflect differing source materials. ?? 1983 Springer-Verlag.

Mineralium Deposita↗
USGS1983

An ion-selective electrode method for determination of chlorine in geological materials

A method is presented for the determination of chlorine in geological materials, in which a chloride-selective ion electrode is used after decomposition of the sample with hydrofluoric acid and separation of chlorine in a gas-diffusion cell. Data are presented for 30 geological standard materials. The relative standard deviation of the method is estimated to be better than 8% for amounts of chloride of 10 μg and greater.

Talanta↗
USGS1983

Geochemistry and economic potential of massive sulfide deposits from the eastern Pacific Ocean

Bulk chemical analyses are performed for major and minor elements using a variety of techniques on a suite of 9 samples of sea floor massive sulfide deposits from 21?N EPR, Juan de Fuca Ridge and Galapagos Rift. Results indicate that deposits at 21?N and Juan de Fuca are very similar despite a geographic separation of 2300 km and are composed primarily of Zn, Fe, and S, with important minor concentrations of Ag, As, Cd and Ge. The Galapagos Rift massive sulfide is primarily Fe, Cu and S and with important minor contents of only Co and Mo. Au is low, ranging from below detection up to 0.17 ppm. Pt group metals are very low, and average about 0.001 ppm. Consideration of enrichment factors and relative metal abundance suggests that MORB is a sufficient source for all the metals enriched in the sea floor deposits. The economically important metals for the 21?N and Juan de Fuca deposits are primarily Zn and Ag, (97%) with potential by-products of Cu, Cd and possibly, Ge. For the Galapagos Rift, the primary value is with Cu (86%) with potential by-products of Co and Mo. The Galapagos Rift deposit is similar to, but contains about twice the Cu content, of typical ore from the Skouriotisa mine of the Troodos complex of Cyprus. The grade of the 21?N/Juan de Fuca deposits is 4 times greater than that of the Galapagos Rift and about twice that of prime deep-sea manganese nodules.

Open-File Report↗
USGS1982

Comparison of platinum, palladium, and rhodium distributions in some layered intrusions with special reference to the late differentiates (upper zone) of the Bushveld Complex, South Africa

The Stillwater, Fiskenaesset, and Bushveld Complexes are all composed of layered ultramafic and mafic rocks in which the cumulus phases generally appear in a regular order, which have similar petrologic and chemical characteristics, which are all Precambrian in age, and which contain platinum-group elements that vary widely in their abundances and relative proportions. Two of the complexes, the Stillwater and Bushveld, contain platinum-group element enriched horizons not yet found in the Fiskenaesset. The ratio of Pt/(Pt + Pd) in rocks from the Stillwater tends to increase from the basal zone to the middle of the ultramafic zone, decreases to the beginning of the banded zone, and then increases again through the banded zone; many fluctuations, however, are superimposed upon this generalized trend. The trends of Pt/(Pt + Pd) ratios appear to show a positive correlation with the Mg/(Mg + Fe (super +2) ) ratio in olivine. In the Fiskenaesset Complex, the Pt/(Pt + Pd) ratio increases rapidly from 0.3 to 0.7 from the lower gabbro and ultramafic units through the leucogabbro units, then increases slowly through the anorthosite and upper gabbro unit. Superimposed on this generalized trend are increasing and decreasing patterns within each unit.Analyses of platinum, palladium, and rhodium for 69 rocks from the main and upper zones of the eastern Bushveld from the Roossenekal area show generally low concentrations of less than 1 ppb Pt; 0.1 ppb Pd; and 0.1 ppb Rh, but larger amounts occur in some magnetite layers and sulfide-bearing zones. Within the main zone up to the pyroxenite marker, from the pyroxenite marker to below lower magnetite layer 2, and in the upper zone, the Pt/(Pt + Pd) ratio decreases with stratigraphic position, although with minor fluctuations in these intervals. The concentration levels of the platinum-group metals appear to be directly related to the amount of sulfide material present and the proportion of intercumulus material. Variations in Pt/(Pt + Pd) ratios in the Bushveld and Fiskenaesset Complexes are presumably related to changes in major mineral compositions as they are in the Stillwater Complex.

Economic Geology↗
USGS1981

Concentration of some platinum-group metals in coal

New data on some platinum group metals in coal indicate that the concentration of Pt is generally less than about 5 ppb, that of Pd is generally less than 1 ppb, and that of Rh is generally less than 0.5 ppb. No conclusive evidence was obtained concerning the mode of occurrence of these elements in coal.

International Journal of Coal Geology↗
USGS1981

Geochemical evidence for modern sediment accumulation on the continental shelf off southern New England

An area of fine-grained sediment approximately 170 km x 74 km in size, located in water depths between 60 m and 150 m, south of Martha's Vineyard, Mass., is a site of modern sediment deposition. The 14 C ages systematically increase with sediment depth from about 1,300 years B.P. at the surface to 8,000-10,000 years B.P. at the depth of maximum core penetration. The old age for the surface sediments probably results from a combination of deposition of old carbon and faunal mixing. In the finest sediments, the sedimentation rates were approximately 130 cm/1,000 yrs when deposition began and have decreased to about 25 cm/1,000 yrs. The decreasing sedimentation rate reflects a diminishing source of fine sediments, which presumably came from the Georges Bank and Nantucket Shoals area. Inventories of excess 210 Pb in undisturbed cores average 70 dpm/cm 2 (disintegrations per minute per square centimeter), more than two times higher than the flux of 210 Pb from the atmosphere and from 226 Ra decay in the overlying water. This additional influx of 210 Pb either must be with new fine-grained sediment material or from solutions that are stripped of their 210 Pb by particulates in the bottom nepheloid layer. Stable Pb concentrations in surface sediments are about 28 ppm, as much as two times higher than concentrations at depth. The high accumulation rates, 210 Pb inventories, and trace-metal profiles imply that this area is a modern sink for fine-grained sediments and for pollutants associated with particulate matter in the water column. To our knowledge, this is the only site of present-day natural deposition on the Continental Shelf off the eastern United States, exclusive of the Gulf of Maine. Because the net currents on the outer half of this Continental Shelf flow from northeast to southwest, this fine-grained deposit may receive its sediments and possible contaminants from the Nantucket Shoals and Georges Bank regions.

Massachusetts↗
USGS1979

The determination of lead in 13 USGS standard rocks

Lead was determined in 13 U.S. Geological Survey standard rocks by graphite furnace atomization and atomic-absorption spectrometry after extraction of lead with diethylammonium diethyldithiocarbamic acid. An analysis of variance of the results obtained from a random sampling of three different bottles of each standard rock showed no heterogeneity among bottles, at the F0.95 level, for a 100-mg sample-size. The relative error of the method, based on the standard deviation of the mean within bottles, was generally less than 10%.

Talanta↗
USGS1977

Thallium contents of 16 USGS standard rocks

Thallium was determined in 16 USGS standard rocks by atomic absorption spectroscopy in which a heated graphite atomizer was used after extraction as thallium iodide into amyl acetate. Four subsamples from four bottles of each standard sample, except G-1 and W-1, were analyzed in random order, and the average thallium contents in parts per million (as Tl) were AGV-1, 0.41; GSP-1, 1.63; G-2, 1.08; BCR-1, 0.35; SDC-1, 0.80; MAG-1, 0.79; BHVO-1, 0.049; SCO-1, 0.79; SGR-1, 0.34; QLO-1, 0.23; RGM-1, 1.07 ; STM-1, 0.30; DTS-1, <0.005; and PCC-1, <0.005. The analysis of variance showed that all samples may be considered homogeneous at F 0.975 and only GSP-1 may be considered heterogeneous at F 0.95 . The Tl contents of G-1 and W-1 are 1.0 and 0.12 ppm, respectively.

Journal of Research of the U.S. Geological Survey↗