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Mineralogic and textural relations in deeply buried rocks of the Simpson Group (Middle Ordovician)--implications in diagenesis and petroleum geology

The mineral composition and petrography of sandstones, shales, carbonates, and intermediate lithologies were determined on 112 core samples of the Middle Ordovician Simpson Group in the Sunray DX Parker No. 1 Mazur well, Grady County, Oklahoma. Core was recovered from present depths of about 15,900-17,200 ft and included all or parts of the Bromide, Tulip Creek, McLish, Oil Creek, and Joins Formations. The bulk-rock mineral composition of Simpson Group rocks is diverse. The mean weighted composition of 50 sandstone samples is 66% quartz, 14% clay, and 18% carbonate, as determined by X-ray powder diffraction (XRD). Some sandstones from the Oil Creek and Tulip Creek Formations contain as much as 96% quartz. These quartz-rich sandstones were cemented early by silica. Feldspar averages 2%; some sandstones from the McLish Formation contain as much as 15% feldspar. Potassium feldspar is commonly more abundant than plagioclase; potassium feldspar overgrowths are found in some of the sandstones. Most of the shales are clay-rich and quartz-poor, averaging about 85% clay minerals, 7% quartz, and 3% feldspar, by weight, as determined by XRD. Carbonate, fluorapatite, and pyrite are present in variable amounts. Such high clay/quartz ratios are not characteristic of shales and suggest that silica has been expelled by diagenetic processes during burial. The main clay mineral in the Simpson Group at these depths is illite, although iron-rich chlorite is locally concentrated in sandstones. Illite typically makes up >90 wt. % of the clay minerals in sandstones and >95 wt. % of those in shale and carbonate. Total clay content, determined from XRD, correlates closely with total gamma-ray intensity from geophysical logs, because illite is the primary potassium-bearing phase in these deeply buried rocks. Therefore, the gamma-ray log is a good indicator of "shaliness" in potential Simpson reservoirs at similar depths. Much of the carbonate was introduced into the sandstones during burial as calcite, dolomite, or ankerite cement. Early iron-free calcite is commonly replaced by iron-bearing calcite, dolomite, or ankerite. Sandstones and carbonate rocks also contain rhombic dolomite. Many of the dolomite rhombs contain overgrowths of ferroan dolomite or ankerite, as evidenced by staining. Ankerite cementation is later and less selective than earlier dolomite and commonly replaces earlier carbonate or silica cements. Dolomite commonly replaces detrital clay and calcite. Spatial and textural relations suggest that the conversion of smectite to illite contributed, in part, to the formation of dolomite and ankerite cements. Scanning electron miscroscopy reveals that much of the diagenetic illite occurs as tabular fibers in pores or as pseudomorphic intergrowths after smectite. Most chlorite in sandstones is authigenic and occurs as a pore-lining cement or as a pseudomorphic replacement after kaolinite. Secondary porosity, formed mainly from the dissolution of intergranular carbonate cements, is best developed in sandstones from the Oil Creek and Tulip Creek Formations.

Oklahoma↗

Mount St. Augustine volcano fumarole wall rock alteration: Mineralogy, zoning, composition and numerical models of its formation process

Intensely altered wall rock was collected from high-temperature (640 °C) and low-temperature (375 °C) vents at Augustine volcano in July 1989. The high-temperature altered rock exhibits distinct mineral zoning differentiated by color bands. In order of decreasing temperature, the color bands and their mineral assemblages are: (a) white to grey (tridymite-anhydrite); (b) pink to red (tridymite-hematite-Fe hydroxide-molysite (FeCl 3 ) with minor amounts of anhydrite and halite); and (c) dark green to green (anhydrite-halite-sylvite-tridymite with minor amounts of molysite, soda and potash alum, and other sodium and potassium sulfates). The alteration products around the low-temperature vents are dominantly cristobalite and amorphous silica with minor potash and soda alum, aphthitalite, alunogen and anhydrite. Compared to fresh 1986 Augustine lava, the altered rocks exhibit enrichments in silica, base metals, halogens and sulfur and show very strong depletions in Al in all alteration zones and in iron, alkali and alkaline earth elements in some of the alteration zones. To help understand the origins of the mineral assemblages in altered Augustine rocks, we applied the thermochemical modeling program, GASWORKS, in calculations of: (a) reaction of the 1987 and 1989 gases with wall rock at 640 and 375 °C; (b) cooling of the 1987 gas from 870 to 100 °C with and without mineral fractionation; (c) cooling of the 1989 gas from 757 to 100 °C with and without mineral fractionation; and (d) mixing of the 1987 and 1989 gases with air. The 640 °C gas-rock reaction produces an assemblage consisting of silicates (tridymite, albite, diopside, sanidine and andalusite), oxides (magnetite and hercynite) and sulfides (bornite, chalcocite, molybdenite and sphalerite). The 375 °C gas-rock reaction produces dominantly silicates (quartz, albite, andalusite, microcline, cordierite, anorthite and tremolite) and subordinate amounts of sulfides (pyrite, chalcocite and wurtzite), oxides (magnetite), sulfates (anhydrite) and halides (halite). The cooling calculations produce: (a) anhydrite, halite, sylvite; (b) Cu, Mo, Fe and Zn sulfides; (c) Mg fluoride at high temperature (> 370 °C); (d) chlorides, fluorides and sulfates of Mn, Fe, Zn, Cu and Al at intermediate temperature (170–370 °C); and (e) hydrated sulfates, liquid sulfur, crystalline sulfur, hydrated sulfuric acid and water at low temperature (< 170°C). The volcanic gas-air mixing calculation produces major amounts of Na and K sulfates, minor amounts of hematite and trace amounts (< 1%) of anhydrite at log gas/air (Ig/a) ratios > 0.41 (> 628°C). This is followed by precipitation of sulfates of Fe, Cu. Pb. Zn and Al at Ig/a ratios between 0.31 and -0.4 (>628-178°C). At a lg/r ratio of ≤ -0.4 (178°C). anhydrous sulfates are replaced by their hydrated forms and hygroscopic sulfuric acid forms. At these low g/a ratios. hydrated sulfuric acid becomes the dominant phase in the system. Comparison of the thermochemical modeling results with the natural samples suggests that the alteration assemblages include: (1) minerals that precipitate from direct cooling of the volcanic gas; (2) phases that form by volcanic gases mixing with air: and (3) phases that form by volcanic gas-air-rock reaction. A complex interplay of the three processes produces the observed mineral zoning. Another implication of the numerical simulation results is that most of the observed incrustation and sublimate minerals apparently formed below 700°C.

Journal of Volcanology and Geothermal Research↗

Geologic reconnaissance of the Al Qunfidhah area, Tihamat Ash Sham quadrangle, Kingdom of Saudi Arabia

Preliminary mineral investigations in the A1 Qunfidhah area, Tihamat Ash Sham quadrangle, indicate that four target zones merit detailed study. These are (1) the West Gossan, (2) the pyrocalstic pile 13 Kilometers of Suq A1 Khamis, (3) the Wadi Sishah copper prospect, and (4) the Wadi Yiba copper prospect. Copper sulfides and carbonates appear to be the most abundant economic minerals present, although nickel, zinc, lead, molybdenum, gold, and silver may also occur in important amounts. In addition to locating specific target zones, the results delimit particular stratigraphic horizons which should be included in future regional mineral investigations. The rocks of the area are comprised of a eugeosynclinal assemblage of Precambrian metavolcanics and metasediments which are intruded by granitic rocks of at least two ages. Rocks which predate the latest granite intrusive are regionally metamorphosed, folded, and faulted. In most cases, zones containing economic minerals occur at or near the top of a volcanic pile and in marine sedimentary, rocks above the volcanic pile. The results from preliminary studies suggest a close genetic relationship between sulfide mineralization and volcanism.

Open-File Report↗

Rock, stream sediment, and heavy-mineral concentrate geochemical data from Unga and western Popof Islands, Alaska Peninsula, Alaska: Chapter 6 in A geological and geophysical study of the gold-silver vein system of Unga Island, Southwestern Alaska

The data reported here was collected during the 1982-1988 mineral resource assessment of the Port Moller and adjacent quadrangles (see Wilson and others, 1996). Analytical data for virtually all of the samples reported here has been previously published in a series of U.S.G.S. Open-File reports, including Angeloni and others (1985), Arbogast and others (1987), and Wilson and others (1987). Induction-coupled plasma (ICP) data is reported here for the first time on stream sediment samples resulting from analyses conducted by S.E. Church in the early 1990's. We have selected a subset of the Port Moller assessment data for inclusion in this report.

Alaska↗

Preliminary report on the mineral resource potential of the Red Rocks Escarpment Instant Study area, Clark County, Nevada

The Red Rocks Escarpment Instant Study area in Clark County, Nevada, is 2 mi (32 km) west of Las Vegas and covers about 31,000 acres (12,500 ha) of the rugged Sandstone Bluffs area in the Spring Mountains (fig. 1). It includes the crest of the range, which is slightly higher than 7,200 ft (2,190 m), the Sandstone Bluffs east of the crest where steep cliffs as high as 2,500 ft (760 m) occur, and part of the gently sloping western range front. The Instant Study area (fig. 2) is within land administered by the U.S. Bureau of Land Management.

Nevada↗

Summary geochemical maps for samples of rock, stream sediment, and nonmagnetic heavy-mineral concentrate, Sweetwater Roadless Area, Mono County, California and Lyon and Douglas Counties, Nevada

The Sweetwater Roadless Area lies between Yerington, Nevada, and Bridgeport, California, along the California-Nevada boundary. The area encompasses approximately 72,240 acres in Toiyabe National Forest in Mono County, California, and Lyon and Douglas Counties, Nevada. This roadless area, which lies just east of the Sierra Nevada range, exhibits rugged topography. Elevations range from about 6,160 feet near Devil's Gate to 11,673 feet at Mount Patterson. Geochemical sampling was conducted during 1978, 1979, and 1980. This report summarizes the results of that investigation and provides details of the geochemical evaluation used in producing the final mineral resource assessment of the study area (Brem and others, 1984). Map A shows the locations of all sites where rock samples were collected for this report and the distributions of anomalous concentrations for 12 elements in the 127 rock samples collected. In a similar manner, map B shows the collection sites for 59 samples of minus-60-mesh stream sediment, and 59 samples of nonmagnetic heavy-mineral concentrate derived from stream sediment and also shows the distributions of anomalous concentrations for 13 elements in the stream-sediment samples and 17 elements in the concentrate samples. Map C shows outlines of those drainage basins containing samples of stream sediment and concentrate with anomalous element concentrations and also shows weighted values for each outlined basin based on the number of elements with anomalous concentrations in each stream-sediment and concentrate sample and on the degree to which these concentrations are anomalous in each sample.

California, Nevada↗