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Leslie F. Ruppert

Publications and source records attributed to Leslie F. Ruppert.

66 records · Page 4Linked to original sources
USGS2002

Arsenic in rocks and stream sediments of the central Appalachian Basin, Kentucky

Arsenic (As) enrichment in coal and stream sediments has been documented in the southern Appalachian basin (see Goldhaber and others, submitted) and is attributed to interaction of rocks and coal with metamorphic fluids generated during the Allegheny Orogeny (late Paleozoic). Similarly derived fluids are expected to affect the coal and in the Kentucky Appalachian Basin to the north as well. In addition, similar processes may have influenced the Devonian oil shale on the western margin of the basin. The major goals of this study are to determine the effect such fluids had on rocks in the Kentucky Appalachian basin (fig. 1), and to understand the geochemical processes that control trace-metal source, residence, and mobility within the basin. This report includes data presented in a poster at the USGS workshop on arsenic (February 21 and 22, 2001), new NURE stream sediment data3 , and field data from a trip in April 2001. Although data for major and minor elements and all detectable trace metals are reported in the Appendices, the narrative of this report primarily focuses on arsenic.

Kentucky↗
USGS1997

Petrography and geochemistry of selected lignite beds in the Gibbons Creek mine (Manning Formation, Jackson Group, Paleocene) of east-central Texas

This study examined the petrographic and geochemical characteristics of two lignite beds (3500 and 4500 beds, Manning Formation, Jackson Group, Eocene) that are mined at the Gibbons Creek mine in east-central Texas. The purpose of the study was to identify the relations among sample ash yield, coal petrography, and trace-element concentrations in lignite and adjoining rock layers of the Gibbons Creek mine. Particular interest was given to the distribution of 12 environmentally sensitive trace elements (As, Be, Cd, Cr, Co, Hg, Mn, Ni, Pb, Sb, Se, and U) that have been identified as potentially hazardous air pollutants (HAPs) in the United States Clean Air Act Amendments of 1990. Eleven lignite, floor, and rock parting samples were collected from incremental channel samples of the 3500 and 4500 beds that were exposed in a highwall of pit A3 at the Gibbons Creek mine. Short proximate and ultimate and forms of sulfur analyses were performed on all lignite samples, and lignite and rock samples were analyzed for 60 major, minor and trace elements. Representative splits of all lignite samples were ground and cast into pellets, and polished for petrographic analyses in blue-light fluorescence and reflected white light to determine liptinite, inertinite, and huminite maceral group percentages. The following observations summarize our results and conclusions about the geochemistry, petrography, and sedimentology of the 3500 and 4500 beds of the Gibbons Creek lignite deposit: (1) Weighted average dry (db) ash yield for the two beds is 29.7%, average total sulfur content is 2.6%, and average calorific value is 7832 Btu (18.22 MJ/kg). Ash yields are greatest in the lower bench (59.33% db) of the 3500 bed and in the upper bench of the 4500 bed (74.61% db). (2) For lignite samples (on a whole-coal basis), the distributions of two of the HAPs (Pb and Sb) are positively related to ash yield, probably indicating an inorganic affinity for these elements. By using cluster analysis we found that Be and Cd were poorly associated with ash yield, indicating a possible organic affinity, and that Ni, Se, Hg, U, and Pb cluster with most of the rare-earth elements. (3) The dominance of the crypto-eugelinite maceral subgroup over the crypto-humotelinite subgroup suggests that all Gibbons Creek lignites were subjected to peat-forming conditions (either biogenic or chemical) conducive to the degradation of wood cellular material into matrix gels, or that original plant material was not very woody and was prone to formation of matrix gels. The latter idea is supported by pollen studies of Gibbons Creek lignite beds; results indicate that the peat was derived in part from marsh plants low in wood tissue. (4) The occurrence of siliceous sponge spicules in the lower benches of the 3500 bed suggests the original peat in this part of the bed was deposited in standing, fresh water. (5) The petrographic data indicate that the upper sample interval of the 3500 bed contains more inertinite (3%) than the other samples studied. Increases in inertinite content in the upper part of the 3500 bed may have been associated with alteration of the peat by acids derived from the volcanic ash or could have been caused by fire, oxidation and drying, or biologic alteration of the peat in the paleo-mire.

International Journal of Coal Geology↗
USGS1997

The origin and distribution of HAPs elements in relation to maceral composition of the A1 lignite bed (Paleocene, Calvert Bluff Formation, Wilcox Group), Calvert mine area, east-central Texas

The origin and distribution of twelve potentially Hazardous Air Pollutants (HAPs; As, Be, Cd, Cr, Co, Hg, Mn, Ni, Pb, Sb, Se, and U) identified in the 1990 Clean Air Act Amendments were examined in relation to the maceral composition of the A1 bed (Paleocene, Calvert Bluff Formation, Wilcox Group) of the Calvert mine in east-central Texas. The 3.2 m-thick A1 bed was divided into nine incremental channel samples (7 lignite samples and 2 shaley coal samples) on the basis of megascopic characteristics. Results indicate that As, Cd, Cr, Ni, Pb, Sb, and U are strongly correlated with ash yield and are enriched in the shaley coal samples. We infer that these elements are associated with inorganic constituents in the coal bed and may be derived from a penecontemporaneous stream channel located several kilometers southeast of the mining block. Of the HAPs elements studied, Mn and Hg are the most poorly correlated to ash yield. We infer an organic association for Mn; Hg may be associated with pyrite. The rest of the trace elements (Be, Co, and Se) are weakly correlated with ash yield. Further analytical work is necessary to determine the mode of occurrence for these elements. Overall, concentrations of the HAPs elements are generally similar to or less than those reported in previous studies of lignites of the Wilcox Group, east-central region, Texas. Petrographic analysis indicates the following ranges in composition for the seven lignite samples: liptinites (5–8%), huminites (88–95%), and inertinites (trace amounts to 7%). Samples from the middle portion of the A1 bed contain abundant crypto-eugelinite compared to the rest of the samples; this relationship suggests that the degradation of plant material was an important process during the development of the peat mire. With the exception of Hg and Mn, relatively low levels of the HAPs elements studied are found in the samples containing abundant crypto-eugelinite. We infer that the peat-forming environment for this portion of the coal bed was very wet with minimal detrital input. Relatively high concentrations of crypto-humotelinite were found in samples from the top and base of the coal bed. The presence of abundant crypto-humotefinite in this part of the coal bed suggests the accumulation of wood-rich peat under conditions conducive to a high degree of tissue preservation in the peat mire. Although several of the trace elements (Be, Co, Ni, and Sb) exhibit enrichment in these samples, they are not necessarily chemically associated with humotelinite. We infer that these elements, with the exception of Be, are possibly associated with deposition of the roof and floor rock of the coal bed; however, further analytical work would be necessary to confirm this hypothesis. Beryllium may have an organic origin.

International Journal of Coal Geology↗
USGS1996

Petrography and geochemistry of the San Miguel lignite, Jackson Group (Eocene), south Texas

The San Miguel lignite deposit (late Eocene, lower Jackson Group) of south Texas consists of four or more thin (generally < 1 m thick) lignite benches that are separated by claystone and mudstone partings. The partings are composed of altered volcanic air-fall ash that has been reworked by tidal or channel processes associated with a back-barrier depositional environment. The purpose of this study is to examine the relationship between the ash yield and the petrographic and geochemical characteristics of the San Miguel lignite as mined. Particular attention is given to 12 of the environmentally sensitive trace elements (As, Be, Cd, Cr, Co, Hg, Mn, Ni, Pb, Sb, Se, and U) that have been identified as possible hazardous air pollutants (HAPs) by the United States Clean Air Act Amendments of 1990. A total of 29 rock and lignite samples were collected and characterized by geochemical and petrographic methods. The major conclusions of the study are as follows: (1) The distribution of Mn is inversely related to the ash yield of the lignite samples. This indicates an organic affinity, or an association with finely disseminated minerals in the lignite that contain this element. (2) On a whole-coal basis, the concentration of the HAPs' element Pb is positively related to ash yield in lignite samples. This indicates an inorganic affinity for Pb. (3) Average whole-coal concentrations of As, Be, Sb, and U in the San Miguel samples are greater than published averages for these elements in other U.S. lignites. (4) The upper and lower lignite benches of the San Miguel deposit are both ash- and algal-rich, indicating that these intervals were probably deposited in wetter conditions than those in which the middle intervals formed. (5) The dominance of the eugelinite maceral subgroup over the huminite subgroup indicates that the San Miguel lignites were subjected to peat-forming conditions (either biogenic or chemical) that enabled degradation of wood cellular material into matrix gels, or that the plants that formed these lignite benches were less woody and more prone to formation of matrix gels. (6) An inertinite-rich layer (top of the B bed) might have formed from widespread oxidation of the San Miguel peat as a result of a volcanic ash fall which was subsequently reworked.

Organic Geochemistry↗
USGS1994

Tonsteins and clay-rich layers in coal-bearing intervals of the Eocene Manning formation, east-central Texas

Six samples from clay-rich intervals in the coal-bearing upper part of the Eocene Manning Formation were analyzed by scanning-electron microscopy and energy-dispersive X-ray fluorescence to determine the origin of minerals in the samples. Two samples were from surface-mine exposures of the 3500 coal bed near Bryan, Texas, and the remaining samples were from an exposure of a correlative interval at the Lake Somerville spillway about 60 km (37 mi) southwest of Bryan. Preliminary data suggest that both a 2-cm-thick (0.75-in) claystone from the upper part of the 3500 bed and the upper part of an 11-cm-thick (4.25-in) mudstone from the floor of the lower coal bed at the spillway were derived from volcanic ash falls. Both clay layers identified as possible tonsteins are composed of kaolinite and accessory quartz, euhedral to subhedral zircon, feldspars, and Ca-Al phosphates (crandallite?). Both alkali and plagioclase feldspars are observed in the two samples, but K-feldspar predominates in the upper clay layer of the 3500 bed, and plagioclase, with accessory Ti-bearing biotite, predominates in the sample from the floor of the spillway. These compositional differences suggest two separate volcanic ash falls. The other sampled clay layers contain rounded to subrounded zircons and feldspars in a mixed-layer clay groundmass, which suggests detrital rather than ash-fall origins.

Texas↗
USGS1993

Differentiation of volcanic ash-fall and water-borne detrital layers in the Eocene Senakin coal bed, Tanjung Formation, Indonesia

The Sangsang deposit of the Eocene Senakin coal bed, Tanjung Formation, southeastern Kalimantan, Indonesia, contains 11 layers, which are thin (<5 cm) and high in ash (> 70%). These layers are characterized by their pelitic macroscopic texture. Examination of eight of the layers by scanning-electron microscopy, energy-dispersive X-ray, and X-ray diffraction analyses show that they are composed primarily of fairly well-crystallized kaolinite, much of which is vermicular. Accessory minerals include abundant Ti oxide, rare-earth element-rich Ca and A1 phosphates, quartz that luminescences in the blue color range, and euhedral to subhedral pyroxene, hornblende, zircon, and sanidine. Although this mineral suite is suggestive of volcanic ash-fall material, only the four pelitic layers in the middle of the bed are thought to be solely derived from volcanic ash-falls on the basis of diagnostic minerals, replaced glass shards, and lithostratigraphic relationships observed in core and outcrop. The three uppermost pelitic layers contain octahedral chromites, some quartz grains that luminesce in teh orange color range, and some quartz grains that contain two-phase fluid inclusions. These layers are interpreted to be derived from a combination of volcanic ash-fall material and hydrologic transport of volcaniclastic sediment. In contrast, the lowermost pelitic layer, which contains large, rounded FeMg-rich chromites, is thought to have been dominantly deposited by water. The source of the volcanic ash-fall material may have been middle Tertiary volcanism related to plate tectonic activity between Kalimantan and Sulawesi. The volcanic ash was deposited in sufficient amounts to be preserved as layers within the coal only in the northern portions of the Senakin region: the southern coal beds in the region do not contain pelitic layers.

southeastern Kalimantan↗
USGS1993

Factors affecting the geochemistry of a thick, subbituminous coal bed in the Powder River Basin: Volcanic, detrital, and peat-forming processes

The inorganic geochemistry and mineralogy of three cores from the Anderson-Dietz 1 coal bed, a 15.2-m-thick subbituminous coal bed in the Tongue River Member (Paleocene) of the Fort Union Formation, were examined (1) to determine if the cores could be correlated by geochemical composition alone over a total distance of 2 km and (2) to identify the major factors that influenced the geochemistry of the coal bed. Chemical data (46 elements on a coal-ash basis) for 81 coal samples and 4 carbonaceous rock samples, with most samples representing a 0.6-m-thick (2-ft) interval of core, were grouped into compositional clusters by means of cluster analysis. Seven major clusters were produced; two of these clusters can be used to correlate the coal bed throughout the study area. Data from scanning electron and optical microscope analyses indicate that several factors influenced the geochemistry of the Anderson-Dietz 1 coal bed. The majority of mineral grains in the coal bed are interpreted to be detrital (water borne); evidence includes the presence of rounded to subrounded quartz grains having two-phase, aqueous fluid inclusions characteristic of hydrothermal or low-to-moderate grade metamorphic quartz. These quartz grains are found throughout the coal bed but are most abundant in samples from the midpart of the bed, which was influenced by detrital input associated with the deposition of the clastic rocks that form the split between the Anderson and Dietz 1 coal beds 900 m to the east of the study area. In addition to the detrital minerals mentioned above, volcanic ash that was fluvially transported to the sites of peat deposition or possibly deposited as air-fall volcanic ash also affected the geochemistry of the coal bed. For example, crandallite(?), a mineral reported to form as an alteration product of volcanic ash, is found in seven samples from the coal bed. The presence of quartz grains containing silicate-melt inclusions in eight samples from the coal bed.provides further support for a volcanic ash component. Other factors that probably affected the geochemistry of the coal bed include (1) detrital input associated with the deposition of the roof rocks of the coal bed, (2) peat-forming processes and plant material, and (3) epigenetic ground-water flow.

Montana, Wyoming↗
USGS1991

Volcanic ash dispersed in the Wyodak-Anderson coal bed, Powder River Basin, Wyoming

Minerals derived from air-fall volcanic ash were found in two zones in the upper Paleocene Wyodak-Anderson coal bed of the Fort Union Formation in the Powder River Basin of Wyoming, and are the first reported evidence of such volcanic material in this thick (> 20 m) coal bed. The volcanic minerals occur in zones that are not visually obvious because they contain little or no clay. These zones were located by geophysical logs of the boreholes and X-ray radiography of the cores. The zones correspond to two of a series of incremental core samples of the coal bed that have anomalous concentrations of Zr, Ba, Nb, Sr, and P 2 O 5 . Two suites of minerals were found in both of the high-density zones. A primary suite (not authigenic) consists of silt-sized quartz grains, biotite, and minor zircon. A minor suite consists of authigenic minerals, including calcite, pyrite, kaolinite, quartz, anatase, barite, and an alumino-phosphate (crandallite?). The original volcanic ash is inferred to have consisted of silica glass containing phenocrysts of quartz, biotite, zircon, and possibly, associated feldspars, pyroxenes, and amphiboles. The glass, as well as the less stable minerals, probably dissolved relatively quickly and contributed to the minor authigenic mineral suite or was removed from the peat as a result of the prevailing hydrologic conditions present in a raised peat formation. This type of volcanic ash suggests that suggests that volcanic material could have rained on the peat; this fallout may have also had a fertilizing effect on the peat by providing nutrients essential for plant growth thus contributing to the thick accumulations of the Wyodak-Anderson bed. Notwithstanding, the presence of these minerals provides evidence for the contribution by volcanic sources to the mineral content of coal, but not as tonsteins.

Wyoming↗
USGS1987

APPLICATIONS OF CATHODOLUMINESCENCE OF QUARTZ AND FELDSPAR TO SEDIMENTARY PETROLOGY.

Cathodoluminescence (CL), the emission of visible light during electron bombardment, was first used in sandstone petrology in the mid-1960's. CL techniques are especially useful for determining the origin and source of quartz and feldspar, two of the most common constituents in clastic rocks. CL properties of both minerals are dependent on their temperature of crystallization, duration of cooling, and/or history of deformation. Detrital quartz and feldspar are typically derived from igneous and metamorphic sources and luminesce in the visible range whereas authigenic quartz and feldspar form at low temperatures and do not luminesce. Quantification of luminescent and non-luminescent quartz and feldspar with the scanning electron microscope, electron microprobe, or a commercial CL device can allow for the determination of origin, diagenesis, and source of clastic rocks when used in conjunction with field and other petrographic analyses.

Scanning Micros↗
USGS1984

ORIGIN OF QUARTZ IN COAL.

Both a scanning electron microscope and an electron microprobe (EMP) were used in this study to analyze the cathodoluminescence properties of quartz grains in samples of the Upper Freeport coal bed because quartz grains in coal are small (silt sized) and below the resolution capabilities of a standard luminoscope. Quartz grains were identified by the detection of silicon alone with energy dispersive X-ray units attached to both the SEM and the EMP.

Conference Paper↗