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Geology of Mount Rainier National Park, Washington

Mount Rainier National Park includes 378 square miles of rugged terrain on the west slope of the Cascade Mountains in central Washington. Its mast imposing topographic and geologic feature is glacier-clad Mount Rainier. This volcano, composed chiefly of flows of pyroxene andesite, was built upon alt earlier mountainous surface, carved from altered volcanic and sedimentary rocks invaded by plutonic and hypabyssal igneous rocks of great complexity. The oldest rocks in the park area are those that make up the Olmnapecosh Formation of late Eocene age. This formation is more than 10,000 feet thick, and consists almost entirely of volcanic debris. It includes some lensoid accumulations of lava and coarse mudflows, heaped around volcanic centers., but these are surrounded by vastly greater volumes of volcanic clastic rocks, in which beds of unstratified coarse tuff-breccia, about 30 feet in average thickness, alternate with thin-bedded breccias, sandstones, and siltstones composed entirely of volcanic debris. The coarser tuff-breccias were probably deposited from subaqueous volcanic mudflows generated when eruption clouds were discharged directly into water, or when subaerial ash flows and mudflows entered bodies of water. The less mobile mudflows and viscous lavas built islands surrounded by this sea of thinner bedded water-laid clastics. In compostion the lava flows and coarse lava fragments of the Ohanapecosh Formation are mostly andesite, but they include less abundant dacite, basalt, and rhyolite. The Ohanapecosh Formation was folded, regionally altered to minerals characteristic of the zeolite facies of metamorphism, uplifted, and deeply eroded before the overlying Stevens Ridge Formation of Oligocene or early Miocene age was deposited upon it. The Stevens Ridge rocks, which are about 3,000 feet in maximum total thickness, consist mainly of massive ash flows. These are now devitrified and altered, but they originally consisted of rhyodacite pumice lapilli and glass shards, which compacted and welded into thick massive units during emplacement and cooling. Subordinate water-laid clastic rocks occur t(ward the top of the formation, and thin-bedded pyroclastic layers occur between some of the ash flows. Exposures on Backbone Ridge and on Carbon River below the mouth of Cataract Creek show that in places the thick basal Stevens Ridge ash flows swept with great violence over an old erosion surface developed on rocks of the Ohanapecosh Formation. Masses of mud, tree trunks, and other surface debris were swirled upward into the base of the lowermost ash fiery, and lobes and tongues of hot ash were forced downward into. the saprolitic mud. The Stevens Ridge Formation is concordantly overlain by the Fifes Peak Formation of probable early Miocene age, which consists of lava flows, subordinate mudflows, and minor quantities of tuffaceous clastic rocks. The lavas are predominantly olivine basalt and basaltic andesite, but they include a little rhyolite. They are slightly to moderately altered: the ferromagnesian phenocrysts are generally replaced by saponite, chiprite, or carbonate ; the glass is devitrified ; and the rocks are locally permeated by veinlets of zeolite. Swarms of diabase sills and dikes are probably intrusive equivalents of the Fifes Peak lavas. The upper part of the Fifes Peak Formation has been mostly eroded from Mount Rainier National Park, but farther north, in the Cedar Lake quadrangle, it attains a thickness of more than 5,000 feet. The Fifes Peak and earlier formations were gently folded, faulted, uplifted, and eroded before the. late Miocene Tatoosh pluton worked its way upward to shallow depths and eventually broke through to the surface. The rise of the pluton was accompanied by .the injection of a complicated melange of satellitic stocks, sills, and dikes. A favored horizon for intrusion of sills was along or near the unconfo

Professional Paper

Hydrogeologic investigations of the Miocene Nogales Formation in the Nogales Area, Upper Santa Cruz Basin, Arizona

Hydrogeologic investigations were conducted to evaluate the groundwater resource potential for the Miocene Nogales Formation in the Nogales area, southern Arizona. Results indicate that parts of the formation may provide new, deeper sources of groundwater for the area. Geologic mapping determined the hydrogeologic framework of the formation by defining lithologic, mineralogic, and stratigraphic characteristics; identifying potential aquifers and confining units; and mapping faults and fractures which likely influence groundwater flow. Geophysical modeling was used to determine the basin geometry and thickness of the Nogales Formation and younger alluvial aquifers and to identify target areas (deep subbasins) which may prove to be productive aquifers. Volcaniclastic sandstone samples from the formation were analyzed for porosity, bulk density, saturated hydraulic conductivity, and fabric. Effective porosity ranges from 16 to 42 percent, bulk density from 1.6 to 2.47 grams per cubic centimeter, and saturated hydraulic conductivity (SHC) from 4 to 57 centimeters per day (4.9×10 -5 to 6.7×10 -4 centimeters per second). Thin sections show that sandstone framework grains consist of quartz, feldspar, biotite, hornblende, pumice, volcanic glass, and opaque minerals. The matrix in most samples consists of pumice fragments, and some contain predominantly silt and clay. Samples with a mostly silt and clay matrix have lower porosity and SHC compared to samples with mostly pumice, which have higher and wider ranges of porosity and SHC. Pore space in the Nogales Formation sediments includes moldic, intercrystalline, and fracture porosity. Some intercrystalline pore space is partially filled with calcite cement. About one third of the samples contain fractures, which correspond to fractures noted in outcrops in all members of the formation. Scanning electron microscope (SEM) and x-ray diffraction (XRD) analyses indicate that most of the samples contained the zeolite clinoptilolite and mixed-layer clay. X-ray diffraction analyses verified clinoptilolite as the only zeolite in Nogales Formation samples; they also verified the presence of smectite and illite clay and some kaolinite. Samples which contain greater amounts of clinoptilolite and lesser amounts of smectite have high porosity and SHC in narrow ranges. However, samples with abundant smectite and lesser amounts of clinoptilolite span the entire ranges of porosity and SHC for the formation. All members of the Nogales Formation are fractured and faulted as a result of Tertiary Basin and Range extensional deformation, which was broadly contemporaneous with deposition of the formation. These structures may have significant influence on groundwater flow in the upper Santa Cruz basin because, although many of the sediments in the formation have characteristics indicating they may be productive aquifers based only on porous-media flow, fracturing in these sediments may further enhance permeability and groundwater flow in these basin-fill aquifers by orders of magnitude.

Arizona

Anomalous solute transport in saturated porous media: Relating transport model parameters to electrical and nuclear magnetic resonance properties

The advection-dispersion equation (ADE) fails to describe commonly observed non-Fickian solute transport in saturated porous media, necessitating the use of other models such as the dual-domain mass-transfer (DDMT) model. DDMT model parameters are commonly calibrated via curve fitting, providing little insight into the relation between effective parameters and physical properties of the medium. There is a clear need for material characterization techniques that can provide insight into the geometry and connectedness of pore spaces related to transport model parameters. Here, we consider proton nuclear magnetic resonance (NMR), direct-current (DC) resistivity, and complex conductivity (CC) measurements for this purpose, and assess these methods using glass beads as a control and two different samples of the zeolite clinoptilolite, a material that demonstrates non-Fickian transport due to intragranular porosity. We estimate DDMT parameters via calibration of a transport model to column-scale solute tracer tests, and compare NMR, DC resistivity, CC results, which reveal that grain size alone does not control transport properties and measured geophysical parameters; rather, volume and arrangement of the pore space play important roles. NMR cannot provide estimates of more-mobile and less-mobile pore volumes in the absence of tracer tests because these estimates depend critically on the selection of a material-dependent and flow-dependent cutoff time. Increased electrical connectedness from DC resistivity measurements are associated with greater mobile pore space determined from transport model calibration. CC was hypothesized to be related to length scales of mass transfer, but the CC response is unrelated to DDMT.

Water Resources Research

Sedimentology of the Argo and Gascoyne abyssal plains, NW Australia: Report on Ocean Drilling Program Leg 123 (Sept. 1–Nov. 1, 1988)

Ocean Drilling Program Leg 123 drilled two sites in the Indian Ocean in order to study the rifting and early spreading of one of the world’s oldest ocean basins. Site 765 was drilled in 5714 meters of water on the Argo Abyssal Plain northwest of Australia. The sedimentary succession records the opening of an ocean basin, from the first sediments deposited atop young oceanic crust, to the present day. The oldest sediments are microlaminated brown silty claystones, locally rich in calcareous bioclasts. Most of the sequence is dominated by turbidites (primarily calcareous) which probably originated within canyons cut into the margin of the drowned platform of the North West Shelf of Australia. Site 766 is located in 3998 meters of water, at the base of the steep western margin of the Exmouth Plateau. The oldest sediments penetrated are glauconitic, volcaniclastic, and bioclastic sandstones and siltstones, which are interbedded with inclined basaltic sills. These sediments were deposited by a prograding submarine fan system which shed shallow marine sediments westward or northwestward off of the western rim of the Exmouth Plateau. Sandstones are succeeded by silty claystones, recording gradual abandonment or redirection of the fan system. An overlying sequence of pelagic and hemipelagic clayey and zeolitic calcareous oozes and chalks is succeeded by featureless and homogeneous pelagic nannofossil oozes.

Argo abyssal plain, Gascoyne abyssal plain

Geologic occurrences of erionite in the United States: an emerging national public health concern for respiratory disease

Erionite, a mineral series within the zeolite group, is classified as a Group 1 known respiratory carcinogen. This designation resulted from extremely high incidences of mesothelioma discovered in three small villages from the Cappadocia region of Turkey, where the disease was linked to environmental exposures to fibrous forms of erionite. Natural deposits of erionite, including fibrous forms, have been identified in the past in the western United States. Until recently, these occurrences have generally been overlooked as a potential hazard. In the last several years, concerns have emerged regarding the potential for environmental and occupational exposures to erionite in the United States, such as erionite-bearing gravels in western North Dakota mined and used to surface unpaved roads. As a result, there has been much interest in identifying locations and geologic environments across the United States where erionite occurs naturally. A 1996 U.S. Geological Survey report describing erionite occurrences in the United States has been widely cited as a compilation of all US erionite deposits; however, this compilation only focused on one of several geologic environments in which erionite can form. Also, new occurrences of erionite have been identified in recent years. Using a detailed literature survey, this paper updates and expands the erionite occurrences database, provided in a supplemental file (US_erionite.xls). Epidemiology, public health, and natural hazard studies can incorporate this information on known erionite occurrences and their characteristics. By recognizing that only specific geologic settings and formations are hosts to erionite, this knowledge can be used in developing management plans designed to protect the public.

Arizona;California;Colorado;Idaho;Montana;New Mexi

The mobility of uranium and other elements during alteration of rhyolite ash to montmorillonite: A case study in the Troublesome Formation, Colorado, U.S.A.

An unusual occurrence of juxtaposed glassy and clay-altered ash was sampled to estimate the degree and type of element mobility during alteration of glass to montmorillonite. The results are particularly interesting in that major mobilization of uranium is indicated. Closely spaced samples of glassy and montmorillonitic ash were collected from the same 20-50 cm thick stratigraphic horizon in the Troublesome Formation (Miocene) of northwestern Colorado. Sharp contacts exist between glassy ash and underlying pink montmorillonite and indicate that water-saturated conditions were restricted to basal ash layers. Formation of montmorillonite instead of zeolites suggests that the water was not highly saline or alkaline. Isotopic and chemical analyses of glassy and clay-altered samples indicate the following: 1. (1) Montmorillonite has U concentrations which are only 10-15% of the concentrations in coexisting glass. Similarly depleted elements include Cs, Rb, Na and K. Much smaller depletions of these elements in some glassy samples serve as sensitive indicators of incipient alteration of glass to montmorillonite. 2. (2) Abundances of relatively insoluble elements such as Th, Ta, Hf and Al are slightly higher (5-50%) in clay-altered ash and serve as indicators of the maximum levels of enrichment in residual material. Greater enrichment of elements such as Ca, Mg, Sr, Sc, P, Cr and Co indicate structural incorporation, adsorption, or ion-exchange uptake by clay or secondary hydrous oxides of Fe and Mn. 3. (3) The rare-earth-element patterns and abundances in glass are sufficiently mimicked by detritus-free montmorillonite to document the compositional equivalency of the two. 4. (4) Radioactive equilibrium exists between 238U and its decay products 234U and 230Th. This documents minimal open-system mobility of U within the last ??? 0.3 Ma. ?? 1982.

Chemical Geology

Mineral-water reactions in metamorphism and volcanism

Low-temperature (120??C and less) metamorphism of graywacke, granite and andesite yields zeolites and precursor gels by reaction with fresh water but low-greenschist facies by reaction with salt (sea)water. ?? 1985.

Chemical Geology

Influence of Shimada Seamount on sediment composition in the eastern tropical North Pacific

Shimada Seamount is a large, young volcanic edifice in the east-central Pacific that is not associated with any active spreading center or known hot spot. The sediments on the abyssal plain surrounding Shimada Seamount consist of pelagic clay with ferromanganese micronodules and zeolites. The pelagic clay is mostly barren of microfossils except for a few occurrences of highly corroded specimens of Radiolaria and diatoms. Eolian terrigenous material is the dominant component of the pelagic clay to a depth of at least 8 m below sea floor, with minor contributions from volcanic debris and hydrothermal and hydrogenous sources. The average amount of basaltic debris is only 0.25%, but concentrations are as high as 10% in some samples. The average hydrothermal component (metalliferous sediment) is 8.8% with a maximum of about 13% at 7.5 m below sea floor in one core. The hydrogenous component, mostly as ferromanganese micronodules, averages 4.1% with a maximum of 5.6%. There is no calcareous biogenic debris and essentially no siliceous biogenic debris. In the past, a decrease in hydrothermal components through time may have been the result of a decrease in relative importance of hydrothermal influences, or an increase in the flux of terrigenous debris transported by the northeast trade winds. Because volcanic activity is still active on Shimada Seamount, or has been in the recent past, the observed increase in relative abundance of terrigenous components probably was the result of increased wind transport and not decreased hydrothermal activity. Shimada Seamount may be an important local source of metalliferous sediment in the eastern equatorial North Pacific, and may have been an even more important source in the past.

Geochimica et Cosmochimica Acta

Geochemistry and diagenesis of Miocene lacustrine siliceous sedimentary and pyroclastic rocks, Mytilinii basin, Samos Island, Greece

A Late Miocene non-marine stratigraphic sequence composed of limestone, opal-CT-bearing limestone, porcelanite, marlstone, diatomaceous marlstone, dolomite, and tuffite crops out on eastern Samos Island. This lacustrine sequence is subdivided into the Hora Beds and the underlying Pythagorion Formation. The Hora Beds is overlain by the clastic Mytilinii series which contains Turolian (Late Miocene) mammalian fossils. The lacustrine sequence contains volcanic glass and the silica polymorphs opal-A, opal-CT, and quartz. Volcanic glass predominantly occurs in tuffaceous rocks from the lower and upper parts of the lacustrine sequence. Opal-A (diatom frustules) is confined to layers in the upper part of the Hora Beds. Beds rich in opal-CT underlie those containing opal-A. The occurrence of opal-CT is extensive, encompassing the lower Hora Beds and the sedimentary rocks and tuffs of the Pythagorion Formation. A transition zone between the opal-A and opal-CT zones is identified by X-ray diffraction patterns that are intermediate between those of opal-CT and opal-A, perhaps due to a mixture of the two polymorphs. Diagenesis was not advanced enough for opal-CT to transform to quartz or for volcanic glass to transform to opal-C. Based on geochemical and mineralogical data, we suggest that the rate of diagenetic transformation of opal-A to opal-CT was mainly controlled by the chemistry of pore fluids. Pore fluids were characterized by high salinity, moderately high alkalinity, and high magnesium ion activity. These pore fluid characteristics are indicated by the presence of evaporitic salts (halite, sylvite, niter), high boron content in biogenic silica, and by dolomite in both the opal-A and opal-CT-bearing beds. The absence of authigenic K-feldspar, borosilicates, and zeolites also support these pore fluid characteristics. Additional factors that influenced the rate of silica diagenesis were host rock lithology and the relatively high heat flow in the Aegean region from Miocene to Holocene.

Samos Island

Lithium-bearing rocks of the Horse Spring Formation, Clark County, Nevada

The Horse Spring Formation of Miocene age in Clark County, Nevada, contains as much as 0.5% Li in individual samples. Rock sequences which average 0.1% Li range from 3 m thick near Gold Butte (south of Mesquite, Nev.) to as much as 40 m thick near Lava Butte (east of Las Vegas, Nev.) about 75 km to the west. The lithium-bearing beds are light colored to white and contain hectorite in a dolomite, magnesite, or calcite matrix. Varied amounts of gypsum, halite, celestite, clinoptilolite, quartz, feldspar, biolite and colemanite are also present locally. Hectorite is the only lithium mineral recognized to date. The lithium-rich rocks contain low concentrations of most other minor elements except that boron and strontium are enriched. Rarely, barium, arsenic, and zinc are present in anomalously large amounts. The lithium-enriched part of the Horse Spring Formation was formed from a series of volcanic ashes which were deposited in a playa. Relict volcanic ash is recognizable in thin sections as remnant glass shards and vitroclastic textures. Most of the original glass has been altered to clay minerals, carbonate minerals, or zeolites, presumably through interaction with highly saline pore waters. Abundant evidence of spring activity suggests that thermal waters played a part in releasing the lithium from volcanic materials.

Nevada

Comparison of hydrothermal alteration of carboniferous carbonate and siliclastic rocks in the Valles caldera with outcrops from the Socorro caldera, New Mexico

Continental Scientific Drilling Program (CSDP) drill hole VC-2B [total depth 1761.7 m (5780 ft); maximum temperature 295 °C] was continuously cored through the Sulphur Springs hydrothermal system in the western ring-fracture zone of the 1.14 Ma Valles caldera. Among other units, the hole penetrated 760.2 m (2494.1 ft) of Paleozoic carbonate and siliciclastic strata underlying caldera fill and precaldera volcanic and epiclastic rocks. Comparison of the VC-2B Paleozoic rocks with corresponding lithologies within and around the 32.1 Ma Socorro caldera, 192 km ( 119 miles) to the south-southwest, provides insight into the variability of alteration responses to similar caldera-related hydrothermal regimes. The Pennsylvanian Madera Limestone and Sandia Formation from VC-2B preserve many of the sedimentological and diagenetic features observed in these units on a regional basis and where unaffected by high temperatures or hydrothermal activity. Micrites in these formations in VC-2B are generally altered and mineralized only where fractured or brecciated, that is, where hydrothermal solutions could invade carbonate rocks which were otherwise essentially impermeable. Alteration intensity (and correspondingly inferred paleopermeability) is only slightly higher in carbonate packstones and grainstones, low to intermediate in siltstones and claystones, and high in poorly cemented sandstones. Hydrothermal fracture-filling phases in these rocks comprise sericite (and phengite), chlorite, allanite, apatite, an unidentified zeolite and sphene in various combinations, locally with sphalerite, galena, pyrite and chalcopyrite. Terrigenous feldspars and clays are commonly altered to chlorite and seriate, and euhedral anhydrite “porphyroblasts” with minor chlorite occur in Sandia Formation siltstone. Fossils are typically unaltered, but the walls of some colonial bryozoans in the Madera Limestone are altered to the assemblage chlorite-sericite-epidote-allanite. La, Ce and Nd are present in an unidentified hydrothermal mineral occurring throughout much of the VC-2B Pennsylvanian sequence. Carboniferous carbonate and siliciclastic formations within and around the Socorro caldera show a similar style of alteration and mineralization to their Valles caldera counterparts, but by contrast locally host commercial, caldera-related, base-metal sulfide deposits. As in the Valles rocks, mineralization and alteration in those of the Socorro caldera were strongly controlled by porosity. Unless disrupted by fractures, breccias, or karst cavities ( not identified in Valles caldera drill holes), the rocks remained relatively unaltered. Where these features allowed ingress of mineralizing hydrothermal solutions, base-metal sulfides and rare-earth-element-bearing minerals were precipitated.

New Mexico

Mineralization dynamics of metakaolin-based alkali-activated cements

This paper investigates the early-age dynamics of mineral formation in metakaolin-based alkali-activated cements. The effects of silica availability and alkali content on mineral formation were investigated via X-ray diffraction and solid-state 29 Si magic-angle spinning nuclear magnetic resonance spectroscopy at 2, 7, 14, and 28 days. Silica availability was controlled by using either liquid- (immediate) or solid-based (gradual) sodium silicate supplements. Mineral (zeolitic) and amorphous microstructural characteristics were correlated with observed changes in bulk physical properties, namely shrinkage, density, and porosity. Results demonstrate that, while alkali content controls the mineralization in immediately available silica systems, alkali content controls the silica availability in gradually available silica systems. Immediate silica availability generally leads to a more favorable mineral formation as demonstrated by correlated improvements in bulk physical properties.

Cement and Concrete Research

Temperature-dependent variations in mineralogy, major element chemistry and the stable isotopes of boron, lithium and chlorine resulting from hydration of rhyolite glass: Constraints from hydrothermal experiments at 150 to 350°C and 25 MPa

Rhyolite-hosted hydrothermal systems in the continental crust contain valuable energy and mineral resources that make them of special interest across several scientific disciplines. Despite extensive research on these systems, the temperature-dependence of chemical reactions between host rocks and aqueous-rich fluids and the mineralogical transformations resulting from these reactions are not well quantified. To expand our understanding of the controlling processes operating in these systems, we carried out seven laboratory experiments in which rhyolite was reacted with deionized water at 150 °C to 350 °C and 25 MPa. An additional experiment at 200 °C was carried out to examine the effect of dissolved CO 2 on the reactions. The overarching goal of this experimental study was to provide new insights on the temperature-dependence of water-rock interaction in continental hydrothermal systems. We applied a wide range of chemical, isotopic and mineralogical methods to analyze the reacted rhyolite and waters, and the major observations are: (1) the rhyolite progressively hydrates with increasing temperature between 150 °C to a maximum of 8.2 wt% H 2 O at 275 °C; hydration then decreases until 350 °C in conjunction with the destruction of the rhyolite glass and crystallization of secondary mineral phases; (2) the ratio of molecular water (H 2 O m ) to hydroxyl (OH − ) of the water that is dissolved in the reacted rhyolite decreases from ∼7 at 150 °C to ∼4 at 250 °C; (3) the main secondary minerals formed are the zeolite ferrierite (T ≥ 275 °C); biotite, albite and cristobalite mainly form at higher experimental temperatures (T ≥ 300 °C); (4) the reacted waters are nearly saturated with respect to amorphous silica; (5) at temperatures ≥ 275 °C nearly all the chlorine is leached into solution; (6) fluorine leaching from the rhyolite gradually increases between 150 °C and 250 °C, but then gradually decreases at higher temperatures and is incorporated into a secondary mineral phase; (7) dissolved CO 2 in the water enhances alkali metal cation leaching from the rhyolite; and (8) calculated Na-K and silica geothermometer temperatures differ from the experimental temperatures by varying amounts. In addition, apart from some small lithium isotope fractionation at temperatures ≤ 250 °C, the stable isotopes of boron, lithium and chlorine do not fractionate during rhyolite-water reactions, and the stable isotope compositions of these species in the reacted water are similar to those in the reactant rhyolite. These results provide new insights for a broad range of applications, including quantifying processes involving rhyolite glass hydration (obsidian hydration dating, perlite formation and discriminating secondary from magmatic water in rhyolitic matrix-glass of volcanic pyroclasts), for geothermal energy and mineral deposit exploration and for monitoring volcanoes.

Geochimica et Cosmochimica Acta

Application of environmental tracers to mixing, evolution, and nitrate contamination of ground water in Jeju Island, Korea

Tritium/helium-3 ( 3 H/ 3 He) and chlorofluorocarbons (CFCs) were investigated as environmental tracers in ground water from Jeju Island (Republic of Korea), a basaltic volcanic island. Ground-water mixing was evaluated by comparing 3 H and CFC-12 concentrations with lumped-parameter dispersion models, which distinguished old water recharged before the 1950s with negligible 3 H and CFC-12 from younger water. Low 3 H levels in a considerable number of samples cannot be explained by the mixing models, and were interpreted as binary mixing of old and younger water; a process also identified in alkalinity and pH of ground water. The ground-water CFC-12 age is much older in water from wells completed in confined zones of the hydro-volcanic Seogwipo Formation in coastal areas than in water from the basaltic aquifer. Major cation concentrations are much higher in young water with high nitrate than those in uncontaminated old water. Chemical evolution of ground water resulting from silicate weathering in basaltic rocks reaches the zeolite–smectite phase boundary. The calcite saturation state of ground water increases with the CFC-12 apparent (piston flow) age. In agricultural areas, the temporal trend of nitrate concentration in ground water is consistent with the known history of chemical fertilizer use on the island, but increase of nitrate concentration in ground water is more abrupt after the late 1970s compared with the exponential growth of nitrogen inputs.

Jeju Island

Formation and use of coal combustion residues from three types of power plants burning Illinois coals

Coal, ash, and limestone samples from a fluidized bed combustion (FBC) plant, a pulverized coal combustion (PC) plant, and a cyclone (CYC) plant in Illinois were analyzed to determine the combustion behavior of mineral matter, and to propose beneficial uses for the power plant ashes. Pyrite and marcasite in coal were converted during combustion to glass, hematite and magnetite. Calcite was converted to lime and anhydrite. The clay minerals were altered to mullite and glass. Quartz was partially altered to glass. Trace elements in coal were partially mobilized during combustion and, as a result, emitted into the atmosphere or adsorbed on fly ash or on hardware on the cool side of the power plants. Overall, the mobilities of 15 trace elements investigated were lower at the FBC plant than at the other plants. Only F and Mn at the FBC plant, F, Hg, and Se at the PC plant and Be, F, Hg, and Se at the CYC plant had over 50% of their concentrations mobilized. Se and Ge could be commercially recovered from some of the combustion ashes. The FBC ashes could be used as acid neutralizing agents in agriculture and waste treatment, and to produce sulfate fertilizers, gypsum wall boards, concrete, and cement. The PC and CYC fly ashes can potentially be used in the production of cement, concrete, ceramics, and zeolites. The PC and CYC bottom ashes could be used in stabilized road bases, as frits in roof shingles, and perhaps in manufacturing amber glass. ?? 2001 Elsevier Science Ltd. All rights reserved.

Fuel

Physical and stable-isotope evidence for formation of secondary calcite and silica in the unsaturated zone, Yucca Mountain, Nevada

Calcite and silica form coatings on fracture footwalls and cavity floors in the welded tuffs at Yucca Mountain, the potential site of a high-level radioactive waste repository. These secondary mineral deposits are heterogeneously distributed in the unsaturated zone (UZ) with fewer than 10% of possible depositional sites mineralized. The paragenetic sequence, compiled from deposits throughout the UZ, consists of an early-stage assemblage of calcite??fluorite??zeolites that is frequently capped by chalcedony??quartz. Intermediate- and late-stage deposits consist largely of calcite, commonly with opal on buried growth layers or outermost crystal faces of the calcite. Coatings on steep-dipping fractures usually are thin (??? 3 mm) with low-relief outer surfaces whereas shallow-dipping fractures and lithophysal cavities typically contain thicker, more coarsely crystalline deposits characterized by unusual thin, tabular calcite blades up to several cms in length. These blades may be capped with knobby or corniced overgrowths of late-stage calcite intergrown with opal. The observed textures in the fracture and cavity deposits are consistent with deposition from films of water fingering down fracture footwalls or drawn up faces of growing crystals by surface tension and evaporated at the crystal tips. Fluid inclusion studies have shown that most early-stage and some intermediate-stage calcite formed at temperatures of 35 to 85??C. Calcite deposition during the past several million years appears to have been at temperatures < 30??C. The elevated temperatures indicated by the fluid inclusions are consistent with temperatures estimated from calcite ??18O values. Although others have interpreted the elevated temperatures as evidence of hydrothermal activity and flooding of the tuffs of the potential repository, the authors conclude that the temperatures and fluid-inclusion assemblages are consistent with deposition in a UZ environment that experienced prolonged heat input from gradual cooling of nearby plutons. The physical restriction of the deposits (and, therefore, fluid flow) to fracture footwalls and cavity floors and the heterogeneous and limited distribution of the deposits provides compelling evidence that they do not reflect flooding of the thick UZ at Yucca Mountain. The textures and isotopic and chemical compositions of these mineral deposits are consistent with deposition in a UZ setting from meteoric waters percolating downward along fracture flow paths.

Applied Geochemistry

Hydrology of Yucca Mountain, Nevada

Yucca Mountain, located in southern Nevada in the Mojave Desert, is being considered as a geologic repository for high-level radioactive waste. Although the site is arid, previous studies indicate net infiltration rates of 5-10 mm yr-1 under current climate conditions. Unsaturated flow of water through the mountain generally is vertical and rapid through the fractures of the welded tuffs and slow through the matrix of the nonwelded tuffs. The vitric-zeolitic boundary of the nonwelded tuffs below the potential repository, where it exists, causes perching and substantial lateral flow that eventually flows through faults near the eastern edge of the potential repository and recharges the underlying groundwater system. Fast pathways are located where water flows relatively quickly through the unsaturated zone to the water table. For the bulk of the water a large part of the travel time from land surface to the potential repository horizon (~300 m below land surface) is through the interlayered, low fracture density, nonwelded tuff where flow is predominately through the matrix. The unsaturated zone at Yucca Mountain is being modeled using a three-dimensional, dual-continuum numerical model to predict the results of measurements and observations in new boreholes and excavations. The interaction between experimentalists and modelers is providing confidence in the conceptual model and the numerical model and is providing researchers with the ability to plan further testing and to evaluate the usefulness or necessity of further data collection.

Reviews of Geophysics

Identification of hydrated silicate minerals on Mars using MRO-CRISM: Geologic context near Nili Fossae and implications for aqueous alteration

[1] The Noachian terrain west of the Isidis basin hosts a diverse collection of alteration minerals in rocks comprising varied geomorphic units within a 100,000 km 2 region in and near the Nili Fossae. Prior investigations in this region by the Observatoire pour l'Minéralogie, l'Eau, les Glaces, et l'Activité (OMEGA) instrument on Mars Express revealed large exposures of both mafic minerals and iron magnesium phyllosilicates in stratigraphic context. Expanding on the discoveries of OMEGA, the Compact Reconnaissance Imaging Spectrometer for Mars (CRISM) aboard the Mars Reconnaissance Orbiter (MRO) has found more spatially widespread and mineralogically diverse alteration minerals than previously realized, which represent multiple aqueous environments. Using CRISM near-infrared spectral data, we detail the basis for identification of iron and magnesium smectites (including both nontronite and more Mg-rich varieties), chlorite, prehnite, serpentine, kaolinite, potassium mica (illite or muscovite), hydrated (opaline) silica, the sodium zeolite analcime, and magnesium carbonate. The detection of serpentine and analcime on Mars is reported here for the first time. We detail the geomorphic context of these minerals using data from high-resolution imagers onboard MRO in conjunction with CRISM. We find that the distribution of alteration minerals is not homogeneous; rather, they occur in provinces with distinctive assemblages of alteration minerals. Key findings are (1) a distinctive stratigraphy, in and around the Nili Fossae, of kaolinite and magnesium carbonate in bedrock units always overlying Fe/Mg smectites and (2) evidence for mineral phases and assemblages indicative of low-grade metamorphic or hydrothermal aqueous alteration in cratered terrains. The alteration minerals around the Nili Fossae are more typical of those resulting from neutral to alkaline conditions rather than acidic conditions, which appear to have dominated much of Mars. Moreover, the mineralogic diversity and geologic context of alteration minerals found in the region around the Nili Fossae indicates several episodes of aqueous activity in multiple distinct environments.

Journal of Geophysical Research E: Planets