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R. I. Grauch

Publications and source records attributed to R. I. Grauch.

At least 19 recordsLinked to original sources
USGS2009

Fossils, lithologies, and geophysical logs of the Mancos Shale from core hole USGS CL-1 in Montrose County, Colorado

As part of a multidisciplinary investigation of Mancos Shale landscapes in the Gunnison Gorge National Conservation Area in Delta and Montrose Counties of western Colorado by the U.S. Geological Survey, Bureau of Land Management, and Bureau of Reclamation, a core of the Upper Cretaceous Mancos Shale was obtained from a borehole, USGS CL-1, in NE1/4 sec. 8, T. 50 N., R. 9 W. (approximately lat 38.61717 degree(s) N., long 107.90174 degree(s) W.), near the town of Olathe. Geophysical records of the borehole include resistivity, gamma ray, and density logs. The core extends between depths of 20 and 557 ft and is about 2.5 in. in diameter. It is composed of calcareous silty shale, as well as scattered beds of limestone and bentonite which were deposited mainly in offshore marine environments during the Cenomanian, Turonian, and Coniacian Stages of the Cretaceous Series. The strata were sampled and analyzed to obtain geochemical data and to identify constituent fossils. Stratigraphic units within the Mancos in the core include the following members, in ascending order: Bridge Creek Limestone (part), Fairport, Blue Hill, Juana Lopez, Montezuma Valley, and Niobrara (part). Strata herein assigned to the Bridge Creek Limestone are about 18 ft thick and consist of silty shale that contains ammonites, bivalves, and a coral of Late Cenomanian age. Strata assigned to the Fairport are about 22 ft thick and composed mainly of calcarenite-bearing, calcareous shale. Fossils in this member include ammonites and bivalves of early middle Turonian age. Overlying the Fairport is the Blue Hill Member, which is about 139 ft thick, and consists of glauconitic, shaley siltstone, and less silty shale. The Juana Lopez Member, overlying the Blue Hill, is about 138 ft thick and composed mainly of calcarenitic, silty shale. Beds in this member contain ammonites and bivalves of late middle and early late Turonian ages. Overlying the Juana Lopez is the Montezuma Valley Member, which is about 55 ft thick and consists of calcarenitic, calcareous silty shale. The Montezuma Valley Member contains ammonites and bivalves of late Turonian age. It is overlain by a lower part of the Niobrara Member of the Mancos Shale which is laterally equivalent to the Fort Hays Limestone Member and part of the overlying Smoky Hill Member of the Niobrara Formation at outcrops in central Colorado. Strata in the core comparable to the Fort Hays are about 39 ft thick and include shaley limestone and calcareous shale, which contain lower Coniacian bivalves. Strata in the core equivalent to part of the Smoky Hill are about 126 ft thick and consist mainly of calcareous silty shale which also contains lower Coniacian bivalves.

Open-File Report↗
USGS2004

Sources of osmium to the modern oceans: New evidence from the 190Pt-186Os system

High precision Os isotope analysis of young marine manganese nodules indicate that whereas the composition of modern seawater is radiogenic with respect to 187Os/188Os, it has 186Os/188Os that is within uncertainty of the chondritic value. Marine Mn nodule compositions thus indicate that the average continental source of Os to modern seawater had long-term high Re/Os compared to Pt/Os. Analyses of loess and freshwater Mn nodules support existing evidence that average upper continental crust (UCC) has resolvably suprachondritic 186Os/188Os, as well as radiogenic 187Os/188Os. Modeling the composition of seawater as a two-component mixture of oceanic/cosmic Os with chondritic Os compositions and continentally-derived Os demonstrates that, insofar as estimates for the composition of average UCC are accurate, congruently weathered average UCC cannot be the sole continental source of Os to seawater. Our analysis of four Cambrian black shales confirm that organic-rich sediments can have 187Os/188Os ratios that are much higher than average UCC, but 186Os/188Os compositions that are generally between those of chondrites and average-UCC. Preferential weathering of black shales can result in dissolved Os discharged to the ocean basins that has a much lower 186Os/188Os than does average upper crust. Modeling the available data demonstrates that augmentation of estimated average UCC compositions with less than 0.1% additional black shale and 1.4% additional ultramafic rock can produce a continental end-member Os isotopic composition that satisfies the requirements imposed by the marine Mn nodule data. The interplay of these two sources provides a mechanism by which the 187Os/188Os of seawater can change as sources and weathering conditions change, yet seawater 186Os/188Os varies only minimally. ?? 2004 Elsevier Ltd.

Geochimica et Cosmochimica Acta↗
USGS2002

Mineralogical characterization of strata of the Meade Peak phosphatic shale member of the Permian Phosphoria Formation: Channel and individual rock samples of measured section J and their relationship to measured sections A and B, central part of Rasmussen Ridge, Caribou County, Idaho

The Permian Phosphoria Formation of southeastern Idaho hosts one of the largest phosphate deposits in the world. Despite the economic significance of this Formation, the fine-grained nature of the phosphorite has discouraged detailed mineralogical characterization and quantification studies. Recently, selenium and other potentially toxic trace elements in mine wastes have drawn increased attention to this formation, and motivated additional study. This study uses powder X-ray diffraction (XRD), with Rietveld quantification software, to quantify and characterize the mineralogy of composite channel samples and individual samples collected from the stratigraphic sections measured by the U.S. Geological Survey in the Meade Peak Member of the Permian Phosphoria Formation at the Enoch Valley mine on Rasmussen Ridge, approximately 15 miles northeast of Soda Springs, Idaho.

Idaho↗
USGS2002

Mineralogical characterization of weathered and less weathered strata of the Meade Peak phosphatic shale member of the Permian Phosphoria Formation: Measured sections E and F, Rasmussen Ridge, and measured sections G and H, Sage Creek area of the Webster Range, Caribou County, Idaho

The Permian Phosphoria Formation of the western U.S. includes one of the largest phosphate deposits in the world. Despite the economic significance of this formation, its fine-grained nature has discouraged detailed mineralogical characterization and quantitative studies. Recently, selenium and other potentially hazardous trace elements in mine wastes have drawn increased attention to these rocks and motivated more extensive study. Part of this effort has focused on a more detailed geological and mineralogical characterization of the rocks. This study uses powder X-ray diffraction (XRD) with Rietveld quantification software to characterize the mineralogy of channel samples from stratigraphic sections measured by the U.S. Geological Survey in the Meade Peak Phosphatic Shale Member of the Permian Phosphoria Formation. Measured sections are at the Rasmussen Ridge mine and at the Smoky Canyon mine approximately 15 and 25 miles, respectively, northeast of Soda Springs, Idaho. The dominant minerals present in these samples are carbonate-fluorapatite, which is the most common phosphatic ore mineral in this and other marine phosphorites, quartz, muscovite, albite, orthoclase, the ammonium feldspar buddingtonite (NH4AlSi3O8), dolomite, and calcite. Because of their potential for hosting trace elements such as Se, the presence of minor pyrite and sphalerite is also noteworthy. Analysis of the carbonate content in the carbonate-fluorapatite by Rietveld refinement shows relatively low carbonate contents, generally between 2 ? 3% (wt.) CO3 2- in the apatite structure, compared to other marine phosphorites.

Idaho↗
USGS2001

Chemical composition of strata of the Meade Peak Phosphatic Shale Member of the Permian Phosphoria Formation: Channel-composited and individual rock samples of measured section J and their relationship of measured sections A and B, central part of Rasmussen Ridge, Caribou County, Idaho

This study, one in a series, reports bulk chemical composition of rock samples collected from a core, referred to as Measured Section J, drilled at a site that subsequently was developed into the Enoch Valley phosphate mine in southeastern Idaho. The core is continuous and cuts through the entire thickness of the Meade Peak Phosphatic Shale Member of the Phosphoria Formation. The steeply dipping Meade Peak extends from 182 to 495 feet below the ground surface, which is the greatest below-ground depth of rock that has been sampled to date. The core was drilled before the start of mining, and the rocks consequently have not been exposed to the atmosphere or surficial weathering processes or fractured as a result of mining as are the rocks from other described sections. Hence, this section of the Meade Peak in the core is the least altered section of this member sampled in this series of studies. The channel-sampled rocks from Section J form a set of contiguous intervals across the entire thickness of the Meade Peak. These channel samples characterize?in ascending order?the lower phosphate ore, interlayered middle waste shale, upper phosphate ore, and upper waste shale units of the member. The Section J channel-sample suite includes 3 composite samples of the uppermost 7 feet of the Grandeur Tongue of the Permian Park City Formation, a dolomitic unit that directly underlies the Meade Peak. It also includes an analysis of a 0.1 foot section of chert directly overlying the Meade Peak. The concentrations of the chemical elements in the channel samples are compared with those of Measured Sections Aand B that were obtained from the same mine. In addition to the channel samples, 85 rock samples were selected from the core to address specific geochemical questions that resulted from examination of the core. For example, several of these samples correspond to cored rock that had unusual concentrations of various elements that were determined using a hand-held, x-ray fluorescence instrument. Other individual samples consist of several samples taken within a short interval of the core that leads to an abrupt change in lithology. Overall, the rocks from Measured Section J exhibit the least alteration from interaction with ground water compared with rocks from any of the measured sections that have been described in our previous studies.

Idaho↗
USGS2001

Stratigraphic section and selected semiquantitative chemistry, Meade Peak phosphatic shale member of Permian Phosphoria Formation, central part of Rasmussen Ridge, Caribou County, Idaho

The U.S. Geological Survey (USGS) has studied the Permian Phosphoria Formation in southeastern Idaho and the entire Western U.S. Phosphate Field throughout much of the twentieth century. In response to a request by the U.S. Bureau of Land Management, a new series of resource, geological, and geoenvironmental studies was undertaken by the USGS in 1998. To accomplish these studies, the USGS has formed cooperative research relationships with two Federal agencies, the Bureau of Land Management and the U.S. Forest Service, tasked with land management and resource conservation on public lands; and with five private companies currently leasing or developing phosphate resources in southeastern Idaho. The companies are Agrium U.S. Inc. (Rasmussen Ridge mine) , Astaris LLC (Dry Valley mine), Rhodia Inc. (Wooley Valley mine, inactive), J.R. Simplot Company (Smoky Canyon mine), and Monsanto Co. (Enoch Valley mine). Some of the mineralogical research associated with this project is supported through a cooperative agreement with the Department of Geology and Geological Enginee ring, University of Idaho. Present studies consist of integrated, multidisciplinary research directed toward (1) resource and reserve estimations of phosphate in selected 7.5-minute quadrangles; (2) elemental residence, mineralogical and petrochemical characteristics; (3) mobilization and reaction pathways, transport, and fate of potentially toxic elements associated with the occurrence, development, and societal use of phosphate; (4) geophysical signatures; and (5) improving the understanding of deposit origin. Because raw data acquired during the project will require time to interpret, the data are released in open-file reports for prompt availability to other workers. Open-file reports associated with this series of studies are submitted to each of the Federal and industry cooperators for comment; however, the USGS is solely responsible for the data contained in the reports.

Idaho↗
USGS1999

Sedimentary exhalative nickel-molybdenum ores in south China

Unique bedded Ni-Mo ores hosted by black shales were discovered in localized paleobasins along the Yangzte platform of southern China in 1971. Textural evidence and radiometric dates imply ore formation during sedimentation of black shales that grade into readily combustible beds, termed stone coals, which contain 10 to 15 percent organic carbon. Studies of 427 fluid inclusions indicate extreme variation in hydrothermal brine salinities that were contained by Proterozoic dolostones underlying the ore zone in Hunan and Guizhou. Variations of fluid inclusion salinities, which range from 0.1 to 21.6 wt percent NaCl equiv, are attributed to differences in the compositions of brines in strata underlying the ore bed, complicated by the presence of sea-water and dilute fluids that represent condensates of vapors generated by boiling of mineralizing fluids or Cambrian meteoric water. The complex processes of ore deposition led to scattered homogenization temperatures ranging from 100 degrees to 187 degrees C within the Hunan ore zone and from 65 degrees to 183 degrees C within the Guizhou ore zone. While living organisms probably did not directly accumulate metals in situ in sufficient amounts to explain the unusually high grades of the deposits, sulfur isotope ratios indicate that bacteria, now preserved as abundant microfossils, provided sufficient sulfide for the ores by reduction of seawater sulfate. Such microbiota may have depended on vent fluids and transported organic matter for key nutrients and are consistent with a sedex origin for the ores. Vent fluids interacted with organic remains, including rounded fragments of microbial mats that were likely transported to the site of ore deposition by the action of waves and bottom currents prior to replacement by ore minerals.

Economic Geology↗
USGS1994

Rhenium and osmium isotopes in black shales and Ni-Mo-PGE-rich sulfide layers, Yukon Territory, Canada, and Hunan and Guizhou provinces, China

Rhenium and osmium abundances and osmium isotopic compositions were determined by negative thermal ionization mass spectrometry for samples of Devonian black shale and an associated Ni-enriched sulfide layer from the Yukon Territory, Canada. The same composition information was also obtained for samples of early Cambrian Ni-Mo-rich sulfide layers hosted in black shale in Guizhou and Hunan provinces, China. This study was undertaken to constrain the origin of the PGE enrichment in the sulfide layers. Samples of the Ni sulfide layer from the Yukon Territory are highly enriched in Re, Os, and other PGE, with distinctly higher Re/ 192 Os but similar Pt/Re, compared to the black shale host. Re-Os isotopic data of the black shale and the sulfide layer are approximately isochronous, and the data plot close to reference isochrons which bracket the depositional age of the enclosing shales. Samples of the Chinese sulfide layers are also highly enriched in Re, Os, and the other PGE. Re/ 192 Os are lower than in the Yukon sulfide layer. Re-Os isotopic data for the sulfide layers lie near a reference isochron with an age of 560 Ma, similar to the depositional age of the black shale host. The osmium isotopic data suggest that Re and PGE enrichment of the brecciated sulfide layers in both the Yukon Territory and in southern China may have occurred near the time of sediment deposition or during early diagenesis, during the middle to late Devonian and early Cambrian, respectively.

Guizhou Province, Hunan Province, Yukon Territory↗