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Elwin L. Mosier

Publications and source records attributed to Elwin L. Mosier.

At least 19 recordsLinked to original sources

Geologic, geochemical, and isotopic studies of a carbonate- and siliciclastic-hosted Pb-Zn deposit at Lion Hill, Vermont

Zn-, Pb-, Cu-, and Fe-bearing rocks of the Lion Hill area in western Vermont formed during the Early Cambrian by syngenetic sedimentary-exhalative and diagenetic replacement processes. Sphalerite, galena, chalcopyrite, pyrite, and, locally, magnetite form stratabound and broadly stratiform lenticular zones, -300 meters long and 25-50 meters thick, which are uneconomic at the present time. The lenses are structurally disrupted and metamorphosed to greenschist facies, probably due to the Taconic orogeny. Textural evidence suggests that mineralizing fluids permeated the sediments prior to lithification and that a dilatant fracture zone, possibly a feeder zone, contains some of the discordant veins at Lion Hill. The veins may have formed when the sediments were in a plastic, semiconsolidated state. The association of layered iron formation containing base-metal sulfide minerals provides possible lithologic evidence for syngenetic mineralization by submarine exhalative activity. Sand bars and tidal channels present in the sedimentary section could have acted as permeable pathways for movement of mineralizing fluids. The complex interlayering in the sedimentary sequence of carbonate and siliciclastic rock types having widely varying permeabilities created numerous fluid traps. Homogenization temperatures of primary and secondary inclusions in vein sphalerite range from 152°C to 196°C; salinities range from 11.5 to 14.0 equivalent weight percent NaCl. δ 34 S values of sulfides from Lion Hill vary from -25.9 to +10.0 per mil, and fall within the expected range for sulfide produced from bacteriogenic reduction of sulfate with δ 34 S values of 25 to 30 per mil. In addition, some pyrite probably formed from sulfate in trapped pore fluid that resulted in heavier isotopic values characteristic of more closed-system behavior. Three sphalerite samples that have heavier sulfur isotopic values may reflect a change in the source of sulfur during a later episode of mineralization, perhaps a change to a deep-seated source. Lead isotopic compositions of galenas from mineralized zones at Lion Hill range from 18.351 to 18.632 for 206 Pb/ 204 Pb, from 15.546 to 15.618 for 207 Pb/ 204 Pb, and from 38.126 to 38.496 for 208 Pb/ 204 Pb. The lead isotopic compositions of galena from Lion Hill and fluid inclusion and sulfur isotopic values for the Lion Hill sulfides are more like those of Pb-Zn-Ag deposits of Ireland than those of MVT or Appalachian-type Zn deposits. The prospect of an Irish-type sedimentary-exhalative origin for stratabound Pb-Zn deposits of the Paleozoic shelf of North America is of considerable importance to understanding the timing of mineralization relative to platform evolution and for evaluating the mineral resource potential of the region. Our study of the Lion Hill deposit indicates a potential for Irish-type Pb-Zn deposits in platform rocks of western Vermont; however, at Lion Hill they contain enrichments of Pb, Zn, and Cu rather than a Pb, Zn, and Ag association.

Vermont↗

Review of the general geology and solid-phase geochemical studies in the vicinity of the Central Oklahoma aquifer

The Central Oklahoma aquifer is the principal source of ground water for municipal, industrial, and rural use in central Oklahoma. Ground water in the aquifer is contained in consolidated sedimentary rocks consisting of the Admire, Council Grove, and Chase Groups, Wellington Formation, and Garber Sandstone and in the unconsolidated Quaternary alluvium and terrace deposits that occur along the major stream systems in the study area. The Garber Sandstone and the Wellington Formation comprise the main flow system and, as such, the aquifer is often referred to as the 'Garber-Wellington aquifer.' The consolidated sedimentary rocks consist of interbedded lenticular sandstone, shale, and siltstone beds deposited in similar deltaic environments in early Permian time. Arsenic, chromium, and selenium are found in the ground water of the Central Oklahoma aquifer in concentrations that, in places, exceed the primary drinking-water standards of the Environmental Protection Agency. Gross-alpha concentrations also exceed the primary standards in some wells, and uranium concentrations are uncommonly high in places. As a prerequisite to a surface and subsurface solid-phase geochemical study, this report summarizes the general geology of the Central Oklahoma study area. Summaries of results from certain previously reported solid-phase geochemical studies that relate to the vicinity of the Central Oklahoma aquifer are also given; including a summary of the analytical results and distribution plots for arsenic, selenium, chromium, thorium, uranium, copper, and barium from the U.S. Department of Energy's National Uranium Resource Evaluation (NURE) Program.

Circular↗

Spectrographic and chemical analyses of whole-rock and insoluble-residue samples, Rolla 1° by 2° quadrangle, Missouri: Drill hole No. 22

Geochemical studies of the Rolla, Mo., 1° x 2° quadrangle were begun in 1977 as part of a joint multidisciplinary study of the quadrangle by the U.S. Geological Survey and the Division of Geology and Land Survey, Missouri Department of Natural Resources. The study is to access the mineral-resource potential of the area by integrated geologic, geochemical, and geophysical studies.

Missouri↗

Spectrographic and chemical analyses of whole-rock and insoluble-residue samples, Rolla 1° x 2° quadrangle, Missouri: Drill hole No. 4

Geochemical studies of the Rolla, Mo., 1° x 2° quadrangle were begun in 1977 as a part of a joint multidisciplinary study of the quadrangle by the U.S. Geological Survey and the Division of Geology and Land Survey, Missouri Department of Natural Resources. The study is to assess the mineral resource potential of the area by integrated geologic, geochemical, and geophysical studies.

Missouri↗

Oxalic-acid leaching of rock, soil, and stream-sediment samples as an anomaly-accentuated technique

In many instances total-rock and sieved-soil and stream-sediment samples lack the sensitivity and contrast required for reconnaissance exploration and necessary in the search for blind ore deposits. Heavy-mineral concentrates incorporate the required sensitivity and contrast but are overly expensive for two reasons: time-consuming sample preparation is required to obtain them, and they cannot be easily derived from all bulk-sample types. Trace-metal-content comparisons of the oxalic-acid-leachable portions with heavy-mineral concentrates show that the leachates are equal to the heavy-mineral concentrates in sensitivity and contrast. Simplicity of preparation and the resultant cost savings are additional advantages of this proposed method.

Open-File Report↗