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At least 217 records · Page 12Linked to original sources

Petrology of Potomac Group sands in Fairfax County, Virginia

The Potomac Group sands sampled in Fairfax County are dominantly microcline-rich lithic arkoses. Quartz averages 59%, microcline 25%, plagioclase less than 1% and lithic grains 16%. Most sands are texturally submature and medium grained. Microcline is somewhat more abundant in the deeper beds in the subsurface than in the shallow subsurface and outcrop sections, with quartz correspondingly more abundant at the surface. Zircon is the only abundant non-opaque heavy mineral in the outcrop section as well as in the shallow subsurface, but tourmaline, rutile and staurolite are also common. In contrast, the lower beds in the subsurface have a heavy mineral assemblage with zircon, garnet and apatite as the dominant species. Several alternative explanations for the vertical variation in mineral assemblages from less to more stable types in the Potomac Group sands are possible: 1) removal of primary Piedmont apatite-bearing igneous and garnet-bearing metamorphic source rock by erosion or burial by overlapping Potomac Group sediments, 2) deep weathering of primary Piedmont source areas and destruction of less stable minerals (apatite and garnet) in Cretaceous time, 3) destruction of less stable minerals (apatite and garnet) near the surface and in the shallow subsurface by post-Cretaceous deep weathering and/or intrastratal solution.

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Geology, petrology, and chemistry of the Leadville Dolomite: host for uranium at the Pitch Mine, Saguache County, Colorado

Newly documented uranium ore in the Pitch Mine occurs chiefly in brecciated Mississippian Leadville Dolomite along the Chester reverse fault zone, and to a lesser extent in sandstone, siltstone, and carbonaceous shale of the Pennsylvanian Belden Formation and in Precambrian granitic rocks and schist. Uranium-mineralized zones are generally thicker, more consistent, and of higher grade in dolomite than in other hosts, and roughly 50 percent of the new reserves are in dolomite. Strong physical control by dolomite is evident, as this is the only lithology that is pervasively brecciated within the fault slices that make up the footwall of the reverse fault zone. Other lithologies tend to either remain unbroken or undergo ductile deformation. Chemical controls are subtle and appear to involve chiefly formation of FeS2 as pyrite and marcasite, which accompany uranium. Leadville Dolomite in the area is about 130 m thick and is predominantly nonfossiliferous dolomicrite. In the Pitch Mine, Leadville Dolomite is bound by faults and maximum known thickness is about 17 m. Mud texture, paucity of fossils and other allochems, thin laminations, and probable algal mat structures suggest sedimentation in a tidal-flat (possibly supratidal) environment. Preservation of mud texture and lack of replacement features indicate that dolomitization was an early, prelithification process, as in modern tidal flats, and produced a chemically and texturally uniform rock over tens of meters with relatively few limestone beds surviving. The sedimentary and diagenetic environment of the tidal-flat dolomite, apparently most favorable for uranium deposits, probably obtained over a large area and should consistute an exploration target over a broad area of central Colorado. Carbonate rocks of the Belden Formation, in contrast to those of the Leadville, contain calcite in great excess of dolomite, more than 5 percent silt-size quartz and clay, and abundant fossils and oolites. Belden limestones (sandy micrite and sandy wackestone) probably were deposited in an intertidal or subtidal environment. Very little uranium ore occurs in these rocks. Chemical aspects, such as the iron, sulfur, and organic carbon contents, are very similar to those of Leadville dolomites, and hence seem favorable, but Belden limestones generally are only mildly fractured. The minor-element content of ore-bearing dolomites is generally normal judging from the relatively scarce data yet published for comparable rocks. Elements enriched in ore include iron, sulfur, molybdenum, and lead. One surface expression of ore in dolomite is ocher-colored, leached, porous gossan that is characterized by residual silica and limonite and by high radioactivity but low chemical uranium content.

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Intrusions and intrusive complexes in an ophiolite near San Luis Obispo; a chemical and petrologic study

The San Luis Obispo ophiolite is a sequence of mafic and ultramafic rocks that lie as a thrust-like slice on top of Franciscan melange in the southern California Coast Range. The ophiolite comprises the classic Steinmann Trinity of basal serpentinized ultramafic rocks overlain sequentially by spilitized pillow lavas and cherts. The ophiolite is intruded by numerous diabasic dikes and several large intrusive complexes that contain peridotite, gabbro, diabase and felsic rocks. Field relations indicate that this ophiolite originated as a sequence of submarine volcanic flows and breccia units extruded onto an ultramafic basement. Later the volcanic and ultramafic rocks were intruded along their contact by mafic magma that crystallized as a stratiform complex of cumulate peridotite and gabbro. Next, this stratiform complex was intruded by diorite and albite-granite (trondhjemite) sills, which may have been produced by partial melting of gabbros in the upper levels of the stratiform complex. Finally all earlier units were intruded by diabasic sills and dikes that probably were late feeders for the pre-existing volcanic unit. All the ophiolite rocks underwent subsequent highly localized brecciation, under greenschist-facies conditions, in which felsic rocks were incipiently melted by frictional heating. The host rocks and intrusions were metamorphosed at low temperature and the mafic rocks were altered by Na- and Si-metasomatism. Despite this pervasive alteration, evidences of the formational stages of the ophiolite are preserved in disequilibrium mineral assemblages, primarily within mafic and ultramafic rocks of the intrusive complexes. Whole-rock analyses of the ophiolite suite indicate that alteration has obscured but not obliterated the original chemical character of the mafic rocks. The ophiolite diabases and basalts contain up to 6 weight percent Na 2 0 and 58 percent Si0 2 , in contrast to normal Si0 2 contents of 50 percent or less and Na 2 0 contents of less than 3 percent for unaltered oceanic and continental tholeiite basalts. However, the low K 2 0 contents (less than 0.8 percent) of all units in the ophiolite suite indicate that these rocks are not part of an alkalic kindred, but rather are altered tholeiites. Compositions of relict amphibole and plagioclase in the mafic rocks indicate that the ophiolite formed in a high-temperature environment and the deep seated rocks were metamorphosed under amphibolite-facies conditions. A later change in the environmental conditions allowed subsequent low-temperature (greenschist facies) metamorphism and metasomatism. The structure and chemistry of the San Luis Obispo ophiolite support the hypothesis that this body may represent a fragment of oceanic crust and mantle. The volcanic rocks and the intrusive complexes probably formed at a mid-ocean ridge, where conditions of high heat-flow provided the requisite high-temperature environment and promoted the production of mafic magmas. The change to low-temperature conditions probably was due to inception or acceleration of crustal spreading at that portion of the ridge where this ophiolite formed. The nature of brecciation in the ophiolite indicates that the low-temperature environment also was one of greater tectonic disturbance, relative to conditions at the ridge. This tectonically active environment probably corresponds to an island arc where the ophiolite-bearing plate was subducted in an adjacent trench. The absence of a high-pressure mineral assemblage in the San Luis Obispo ophiolite suggests that this segment of ocean-crust and upper mantle was not buried in a subduction zone, but rather was rafted on top of subduction melange (Franciscan Formation) into its present position.

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Eruptive history, petrology, and petrogenesis of the Joe Lott Tuff Member of the Mount Belknap Volcanics, Marysvale volcanic field, west-central Utah

The Joe Lott Tuff Member of the Mount Belknap Volcanics is the largest rhyolitic ash-flow tuff sheet in the Marysvale volcanic field. It was erupted 19 m.y. ago, shortly after the changeover from intermediate-composition calc-alkalic volcanism to bimodal basalt-rhyolite volcanism. Eruption of the tuff resulted in the formation of the Mount Belknap Caldera whose pyroclastic intracaldera stratigraphy parallels that in the outflow facies. The Joe Loft Tuff Member is a composite ash-flow sheet that changes laterally from a simple cooling unit near the source to four distinct cooling units toward the distal end. The lowest of these units is the largest and most widespread; it is 64 m thick and contains a basal vitrophyre. Eruption of the lower unit led to the initial collapse of the caldera. The lower unit is followed upward by a 43 m middle unit, a 26 m pink-colored unit which is separated by a prominent air- fall layer, and a 31 m upper unit. The Joe Loft Tuff Member is an alkali rhyolite with 75.85-77.31 wt. % silica and 8.06-9.32 wt. % K2O+Na2O; the agpaitic index (Na2O+ K2O/Al2O3) is .77-.98. The tuff contains about I% phenocrysts of quartz, sanidine, oligoclase, augite, apatite, zircon, sphene, biotite, and oxidized Fe-Ti oxides. The basal vitrophyre contains accessory allanite, chevkinite, and magnesiohastingsite. The main cooling units are chemically and mineralogically zoned indicating that the magma chamber restratified prior to each major eruption. Within each of the two thickest cooling units, the mineralogy changes systematically upwards; the Or content and relative volume of sanidine decreases and An content of plagioclase increases. The basal vitrophyre of the lower unit has a bulk composition that lies in the thermal trough near the minima of Or-Ab-Q at 1 kb PH2O. Microprobe analyses of feldspar and chemical modeling on experimental systems indicate that pre-eruption temperatures were near 750?C and that the temperature increased during the eruption of the cooling units. The chemical gradients in the apatite and whole-rock data in the Joe Loft Tuff Member and the consistent mineral assemblages throughout the ash-flow cannot be explained by crystal settling. The fractionation of the Joe Lott Tuff Member appears to closer fit the model of convection-driven thermogravitational diffusion.

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