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At least 703 records · Page 39Linked to original sources

USGS1994

Effects of sediment depositional environment and ground-water flow on the quality and geochemistry of water in aquifers in sediments of Cretaceous age in the coastal plain of South Carolina

The quality and geochemistry of ground water are significantly affected by the depositional environment of aquifer sediments. Cretaceous sediments in the Coastal Plain of South Carolina have been deposited in fluvial, delta-plain, marginal-marine, and marine environments. Depositional environments of sediments within a single aquifer may grade from nonmarine, fluvial, or upper delta plain near the updip limit of the aquifer to transitional, lower delta plain and to marine toward the coast. In nonmarine sediments the major source of inorganic carbon in the water is the decomposition of organic material. The major aqueous geochemical processes are the dissolution and alteration of silicate minerals. Silica makes up a major part of the dissolved constituents in water from these sediments. In transitional and marine sediments the major aqueous geochemical processes are (1) the dissolution of calcium carbonate by hydrolysis and by carbonic acid derived from the decomposition of organic material and (2) the exchange of calcium in solution for sodium on the marine-clay minerals. The clay minerals may also serve as buffers by neutralizing the hydroxyl ion produced by hydrolysis. The effects of incompletely flushed dilute saltwater on water quality increase toward the coast and toward the northeast.

South Carolina↗

USGS2011

Episodic soil succession on basaltic lava fields in a cool, dry environment

Holocene- to late Pleistocene-aged lava flows at Craters of the Moon National Monument and Preserve provide an ideal setting to examine the early stages of soil formation under cool, dry conditions. Transects were used to characterize the amount and nature of soil cover on across basaltic lava flows ranging in age from 2.1 to 18.4 ka. Results indicate that on flows <13 ka, very shallow organic soils (Folists in Soil Taxonomy) are the dominant soil type, providing an areal coverage of up to &sim;25%. On flows ≥13.9 ka, deeper mineral soils including Entisols, Aridisols, and Mollisols become dominant and the areal extent increases to ≥95% on flows older than 18.4 ka. These data suggest there are two distinct pedogenic pathways associated with lava flows of the region. The first pathway is illustrated by the younger flows, where Folists dominate. In the absence of a major source of loess, relatively little mineral material accumulates and soils provide only minor coverage of the lava flows. Our results indicate that this pathway of soil development has not changed appreciably over the past &sim;10 ka. The second pedogenic pathway is illustrated by the flows older than 13.9 ka. These flows have been subject to deposition of large quantities of loess during and after the last regional glaciation, resulting in almost complete coverage. Subsequent pedogenesis has given rise to Aridisols and Mollisols with calcic and cambic horizons and mollic epipedons. This research highlights the importance of regional climate change on the evolution of Craters of the Moon soilscapes.

Idaho↗

USGS2009

Trace elements in Zn Pb Ag deposits and related stream sediments, Brooks Range Alaska, with implications for Tl as a pathfinder element

The Zn-Pb-Ag metallogenic province of the western and central Brooks Range, Alaska, contains two distinct but mineralogically similar deposit types: shale-hosted massive sulphide (SHMS) and smaller vein-breccia occurrences. Recent investigations of the Red Dog and Anarraaq SHMS deposits demonstrated that these deposits are characterized by high trace-element concentrations of As, Ge, Sb and Tl. This paper examines geochemistry of additional SHMS deposits (Drenchwater and Su-Lik) to determine which trace elements are ubiquitously elevated in all SHMS deposits. Data from several vein-breccia occurrences are also presented to see if trace-element concentrations can distinguish SHMS deposits from vein-breccia occurrences. Whole-rock geochemical data indicate that Tl is the most consistently and highly concentrated characteristic trace element in SHMS deposits relative to regional unmineralized rock samples. Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) analyses of pyrite and sphalerite indicate that Tl is concentrated in pyrite in SHMS. Stream sediment data from the Drenchwater and Su-Lik SHMS show that high Tl concentrations are more broadly distributed proximal to known or suspected mineralization than As, Sb, Zn and Pb anomalies. This broader distribution of Tl in whole-rock and particularly stream sediment samples increases the footprint of exposed and shallowly buried SHMS mineralization. High Tl concentrations also distinguish SHMS mineralization from the vein-breccia deposits, as the latter lack high concentrations of Tl but can otherwise have similar trace-element signatures to SHMS deposits. ?? 2009 AAG/Geological Society of London.

Geochemistry: Exploration, Environment, Analysis↗

USGS2001

A metallogenic survey of alkalic rocks of Mt. Somma-Vesuvius volcano

Somma-Vesuvius is an alkaline volcano whose products (pumice, scoria and lava) have alkaline (Na2O+K2O) contents between 6 and 16 wt%, Mg number <50, SiO2 59-47 wt% and MgO 0-7.8 wt% (more than 50% of the samples have a content <2 wt%). Immobile-element ratios (Th/Yb, Ta/Yb, Ce/Yb) indicate a shoshonitic character, while the K2O content (4-10 wt%) is characteristic of ultrapotassic rocks. The behavior of selected metals is discussed by grouping them on the basis of the stratigraphic sequence and differentiating the volcanic activity between plinian and interplinian (Rolandi et al., 1998; Ayuso et al., 1998). This allows observation of the variation within each formation from 25.000y. BP to the last historic eruptive cycle (1631-1944 AD). The main processes to explain the wide distribution of the data presented are fractional crystallization of a mantle-derived magma, magma mixing, and contamination with heterogeneous lower and/or upper crust. Variation diagrams distinguish different behavior for groups of metals: Ag (0.01-0.2 ppm), Mo (1-8.8 ppm), W (1.3-13 ppm), Pb (16-250 ppm), Sb (0.2-2.6 ppm), Sc (0.2-61 ppm), Li (15-140 ppm) and Be (1-31 ppm) increase with increasing differentiation and tend to correlate with the incompatible trace elements (Th, Hf, etc). Cu (10-380 ppm), Au (2-143 ppb), Co (0.7-35.1 ppm) and Fe (1.3-6.2 wt%) decrease towards advanced stage of differentiation. Iron also identifies three magmatic groups. The ratio Fe3+/Fe2+ ranges between 0.2 and 1.8, and Fe2O3/ (Fe2O3+FeO) ranges between 0.2 and 0.8, giving rise to an oxidized environment; exceptions are in the samples belonging to the interplinian formations: I, II, medieval and 1631-1994 AD. Fluorine ranges between 0.1 and 0.4 wt% for the complete Mt. Somma-Vesuvius activity, except for the Ottaviano and Avellino plinian (0.8 wt%) events. Chlorine has a wider range, from 0.1 wt% to 1.6 wt%. Mt Somma-Vesuvius has some features similar to those of mineralized alkaline magmatic systems which coincide with the transition between subduction-related compression and extension-related to continental rifting. We infer that a prospective time for the formation of mineralization at Mt Somma-Vesuvius was during the 1631-1944 eruptive period.

Mineralogy and Petrology↗

USGS2016

New perspectives on a 140-year legacy of mining and abandoned mine cleanup in the San Juan Mountains, Colorado

The Gold King mine water release that occurred on 5 August 2015 near the historical mining community of Silverton, Colorado, highlights the environmental legacy that abandoned mines have on the environment. During reclamation efforts, a breach of collapsed workings at the Gold King mine sent 3 million gallons of acidic and metal-rich mine water into the upper Animas River, a tributary to the Colorado River basin. The Gold King mine is located in the scenic, western San Juan Mountains, a region renowned for its volcano-tectonic and gold-silver-base metal mineralization history. Prior to mining, acidic drainage from hydrothermally altered areas was a major source of metals and acidity to streams, and it continues to be so. In addition to abandoned hard rock metal mines, uranium mine waste poses a long-term storage and immobilization challenge in this area. Uranium resources are mined in the Colorado Plateau, which borders the San Juan Mountains on the west. Uranium processing and repository sites along the Animas River near Durango, Colorado, are a prime example of how the legacy of mining must be managed for the health and well-being of future generations. The San Juan Mountains are part of a geoenvironmental nexus where geology, mining, agriculture, recreation, and community issues converge. This trip will explore the geology, mining, and mine cleanup history in which a community-driven, watershed-based stakeholder process is an integral part. Research tools and historical data useful for understanding complex watersheds impacted by natural sources of metals and acidity overprinted by mining will also be discussed.

Colorado↗

USGS1998

Geologic studies in Alaska by the U.S. Geological Survey, 1996

This collection of 12 papers continues the annual series of U.S. Geological Survey (USGS) reports on geologic investigations in Alaska. The annual volume presents results from new or ongoing studies in Alaska that are of interest to scientists in academia, industry, land and resource managers, and the general public. The Geological Studies in Alaska volume reports the results of studies that cover a broad spectrum of earth science topics from many parts of the state (fig. 1). The papers in this volume are organized under the topics Environment and Climate, Resources, and Geologic Framework, in order to reflect the objectives and scope of USGS programs that are currently active in Alaska. Environmental studies are the focus of two articles in this volume: One study addresses the relation between glaciers and aquatic habitat on the Kenai River and another study evaluates the geochemistry of water draining chromite deposits in Alaska. Two papers address mineral resources in southwestern Alaska including a geochemical study of the Fortyseven Creek prospect and a geological and geochemical study of the Stuyahok area. Eight geologic framework studies apply a variety of techniques to a wide range of subjects throughout Alaska, including biostratigraphy, geochemistry, geochronology, paleomagnetism, sedimentology, and tectonics. Two bibliographies at the end of the volume list reports about Alaska in USGS publications released in 1996 and reports about Alaska by USGS authors in non-USGS publications in 1996.

Alaska↗

USGS1981

Geologic controls of uranium mineralization in the Tallahassee Creek uranium district, Fremont County, Colorado.

Two important orebodies have been defined by drilling in the Tallahassee Creek uranium district, Fremont County, Colorado, namely the Hansen and the Picnic Tree. Host rocks are respectively the upper Eocene Echo park Alluvium, and the lower Oligocene Tallahassee Creek Conglomerate. Average ore grade is about 0.08% U3O8. The principal source rock is the lower Oligocene Wall Mountain Tuff. Leaching and transportation of the uranium occurred in alkaline oxidizing ground water that developed during alteration of the ash in a semi-arid environment. The uranium was transported in the groundwater and deposited in a reducing environment controlled by carbonaceous material and associated pyrite. Localization of the ore was controlled by groundwater flow conditions and by the distribution of organic matter in the host rock. -from Author

Mountain Geologist↗

USGS2009

Changing sources of strontium to soils and ecosystems across the Hawaiian Islands

Strontium isotope ratios assist ecosystem scientists in constraining the sources of alkaline earth elements, but their interpretation can be difficult because of complexities in mineral weathering and in the geographical and environmental controls on elemental additions and losses. Hawaii is a "natural laboratory" where a number of important biogeochemical variables have either limited ranges or vary in systematic ways, providing a unique opportunity to understand the impact of time, climate, and atmospheric inputs on the evolution of base cation sources to ecosystems. There are three major sources of strontium (Sr) to these ecosystems, each with distinct isotopic compositions: basalt lava, Asian dust, and rainfall. We present Sr isotope and concentration data on both bulk soil digests and NH 4 Ac extracts from soil profiles covering a wide range of environments and substrate ages. Bulk soil material from dry climates and/or young substrate ages with > 80????g g - 1 Sr retain basalt-like Sr isotopic signatures, whereas those with Sr concentrations < 80????g g - 1 can have isotope signatures that range from basalt-like values to the more radiogenic values associated with continental dust. Although both dust accumulation and lava weathering are time- and rainfall-dependent, the overall concentration of Sr drops with increasing leaching even as quartz and mica derived from continental dust sources increase to > 40% by mass. At elevated dust levels, lava-derived Sr is low and dust-derived Sr is the dominant control of 87 Sr/ 86 Sr in bulk soils; however, 87 Sr/ 86 Sr of NH 4 Ac-extractable Sr largely reflects atmospheric deposition of marine aerosol in these situations. Overall, whole-soil Sr isotope values are controlled by complex interactions between Sr provided by lava weathering but partially lost by leaching, and Sr provided by dust but held in more resistant minerals. The isotopic composition of NH 4 Ac-extractable Sr and of the biota is controlled by lava weathering and rainfall contribution of Sr with only minor contributions from radiogenic dust sources. ?? 2009 Elsevier B.V.

Chemical Geology↗

USGS2010

Limited hydrologic response to Pleistocene climate change in deep vadose zones - Yucca Mountain, Nevada

Understanding the movement of water through thick vadose zones, especially on time scales encompassing long-term climate change, is increasingly important as societies utilize semi-arid environments for both water resources and sites viewed as favorable for long-term disposal or storage of hazardous waste. Hydrologic responses to Pleistocene climate change within a deep vadose zone in the eastern Mojave Desert at Yucca Mountain, Nevada, were evaluated by uranium-series dating of finely layered hyalitic opal using secondary ion mass spectrometry. Opal is present within cm-thick secondary hydrogenic mineral crusts coating floors of lithophysal cavities in fractured volcanic rocks at depths of 200 to 300 m below land surface. Uranium concentrations in opal fluctuate systematically between 5 and 550 μg/g. Age-calibrated profiles of uranium concentration correlate with regional climate records over the last 300,000 years and produce time-series spectral peaks that have distinct periodicities of 100- and 41-ka, consistent with planetary orbital parameters. These results indicate that the chemical compositions of percolating solutions varied in response to near-surface, climate-driven processes. However, slow (micrometers per thousand years), relatively uniform growth rates of secondary opal and calcite deposition spanning several glacial–interglacial climate cycles imply that water fluxes in the deep vadose zone remained low and generally buffered from the large fluctuations in available surface moisture during different climates.

Nevada↗

USGS1999

Utility of EXAFS in characterization and speciation of mercury-bearing mine wastes

Extensive mining of large mercury deposits located in the California Coast Range has resulted in mercury contamination of both the local environment and water supplies. The solubility, dispersal, and ultimate fate of mercury are all affected by its chemical speciation, which can be most readily determined in a direct fashion using EXAFS spectroscopy. EXAFS spectra of mine wastes collected from several mercury mines in the California Coast Range with mercury concentrations ranging from 230 to 1060 mg/kg (ppm) have been analyzed using a spectral database of mercury minerals and sorbed mercury complexes. While some calcines have been found to consist almost exclusively of mercuric sulfide, HgS, others contain additional, more soluble mercury phases, indicating a greater potential for the release of mercury into solution. This experimental approach can provide a quantitative measurement of the mercury compounds present and may serve as an indicator of the bioavailability and toxicity levels of mercury mine wastes.

Journal of Synchrotron Radiation↗

USGS1981

Geology and concepts of genesis of important types of uranium deposits

Uranium ore deposits occur in nearly every major rock type in the earth’s crust, and nearly all igneous, metamorphic, and sedimentary processes are capable of concentrating or dispersing uranium. However, only three types of deposits account for more than 70 percent of known Western World Reasonably Assured Resources (WWRAR): Precambrian quartz-pebble conglomerate type, Proterozoic unconformity type, and Phanerozoic sandstone type. Igneous-related processes in plutonic, volcanic, and magmatic-hydrothermal environments, considered important 25 years ago, now account for less than 10 percent of world resources known at present. The oldest known ore deposits were formed in conglomerates by placer processes under unique anoxic conditions. For the last 2.2 b.y., since oxygenation of the atmosphere, the genesis of both high- and low-temperature deposits has been dominated by three general geochemical processes: (1) oxidation of uranium to soluble U(VI) species permitting aqueous transport, perhaps most commonly as uranyl-carbonate complexes; (2) reduction, principally by C, S −2 , or Fe +2 species, to U(IV) to allow precipitation of uraninite (pitchblende), and coffinite, although the specific reductant commonly cannot be determined because these three tend to be associated geologically; and (3) igneous and metamorphic differentiation caused by exclusion of uranium from crystal structure of most rock-forming minerals. The geochemistry of uranium ore-forming processes has changed in time because of the evolution of life forms and their impact on the earth’s oxygen and carbon budgets. This evolution is reflected in changing predominance of ore types in geologic time: (1) pre-2.8 b.y. ago—no known uranium ore deposits; (2) ca. 2.8 to 2.2 b.y. ago—the first intràcratonic basins and anoxic atmosphere permitted accumulation of placer deposits of uraninite in quartz-pebble conglomerates; these deposits contain about 19 percent of the western world’s resources; (3) ca. 2.2 to 0.4 b.y. ago—following oxygenation of the atmosphere uranium was oxidized and transported as soluble U(VI) complexes to sites of reduction, commonly in organic carbon-rich marginal marine environments. Diagenesis, metamorphism, and near-surface redox enrichment subsequently formed unconformity-type, ultrametamorphic-type, and vein-type ore deposits which together contain more than 25 percent of the western world’s resources; (4) ca. 0.4 b.y. ago to present—after development of land plants the most important ore-forming process was redox-controlled deposition from ground water in continental sediments. Sandstone-type deposits, characteristic of this stage, contain about 40 percent of the western world’s resources.

Book chapter↗

USGS1981

Factors affecting the partitioning of Cu, Zn and Pb in boulder coatings and stream sediments in the vicinity of a polymetallic sulfide deposit

A sequential extraction scheme is utilized to determine the geochemical partitioning of Cu, Zn and Pb among hydrous Mn- and Fe-oxides, organics and residual crystalline silicates and oxides in the minus-80-mesh (< 0.18 mm) sediments and in boulder coatings from a stream in Lincoln County, Georgia (U.S.A.). The stream drains an area containing a CuZnPb-sulfide deposit (Magruder Mine). The boulder coatings contain mainly Mn-oxides and organics, with minor hydrous Fe-oxides. In the sediment, the chemically active phases are mainly hydrous Fe-oxides and organics, probably because Mn is leaching out of the sediments and precipitating on the exposed surfaces of boulders. In the boulder coatings, competition among Fe- and Mn-oxides and organics for Cu, Zn and Pb follows the order: Cu, organics > Fe-oxides > Mn-oxides; Zn, Mn-oxides {reversed tilde equals} organics > Fe-oxides; Pb, Fe-oxides > organics > Mn-oxides. In the sediments, organics are the most efficient scavengers of all three ore metals. These results emphasize the importance of organics as sinks for the ore metals, even in environments with high concentrations of Mn- and Fe-oxides. Of the ore metals, Zn appears to be the most mobile, and is partitioned most strongly into the coatings. However, anomaly contrast for hydromorphic Zn, normalized to the MnFe-oxide or organic content, is similar in sediments and coatings. Cu shows the highest anomaly on the boulder coatings, probably due to precipitation of a secondary Cu mineral. In contrast, detrital Pb in the pan concentrates shows a better anomaly than any hydromorphic Pb component. ?? 1981.

Chemical Geology↗

USGS1985

Geologic setting, petrology, and geochemistry of stratiform sphalerite-galena-barite deposits, Red Dog Creek and Drenchwater Creek areas, northwestern Brooks Range, Alaska

Similar stratiform sphalerite-galena-barite deposits occur in the Red Dog Creek area, De Long Mountains quadrangle, and in the Drenchwater Creek area, Howard Pass quadrangle, northwestern Brooks Range, Alaska. The deposits, located approximately 180 km apart, are hosted by Mississippian and Pennsylvanian strata of the Kagvik structural sequence of late Paleozoic and early Mesozoic age. This sequence is situated in the lowermost structural plate of a series of predominantly east-striking, shallow-dipping thrust plates that characterize the regional structure. The deposits occur in shale, tuff, tuffaceous sandstone, altered chert, and quartz exhalite. These units are in places interlayered with or adjacent to bedded or nodular barite or submarine keratophyre flows. Chert and shale commonly contain abundant highly altered, fine-grained feldspar, pumice lapilli, and mafic volcanic rock fragments.The main types of occurrences at Red Dog Creek are: (1) disseminated and stratiform sulfides thinly bedded in organic-rich Mississippian and Pennsylvanian shale and chert, (2) massive sulfide veins and breccia fillings in silicified Mississippian and Pennsylvanian shale, and (3) stratiform sulfide-bearing lenses subdivided into (3a) quartz-exhalite with up to several percent sulfides and barite, (3b) massive sulfide-quartz lenses with up to several percent barite, and (3c) barite-quartz lenses with up to several percent sulfides.At Drenchwater Creek sulfides and barite occur as: (1) disseminations in shale, chert, tuff, and tuffaceous sandstone; (2) disseminations to aggregates in quartz exhalite; and (3) occurrences in veins crosscutting cleavages in brecciated chert and shale.The stratiform sulfides occur in zones up to several thousand meters long and several tens of meters thick. Preliminary grades at Red Dog Creek are 17.1 percent zinc, 5.0 percent lead, and 2.4 oz silver per ton contained in at least 85 million tons.The range of sulfide sulfur isotope values at Red Dog Creek is -16.6 per mil to +3.6 per mil. Sphalerite averages 0.8 per mil. Pyrite is isotopically lighter than coexisting sphalerite in quartz exhalite and massive sulfide lenses. This isotopic relationship is compatible with paragenetic relationships which show pyrite crystallized both earlier and later than other sulfides. Galena is isotopically lighter than coexisting sphalerite. Three groups of geologically and isotopically distinct barites exist including isotopic values appropriate for derivation from late Paleozoic seawater sulfate.Early in the depositional sequence isotopically light pyrite formed from organically reduced seawater sulfate. Sphalerite, galena, late pyrite, and some barite precipitated from two sulfur-bearing solutions that mixed at the mineralization site. Isotopically light barite associated with sulfides precipitated from oxidized H 2 S without seawater sulfate contribution. Lead isotope data from Red Dog and Drenchwater Creeks are compatible with generation of lead in a Phanerozoic mature island-arc setting, a typical orogene, or possibly a back-arc type intracratonic basin.The stratiform sphalerite-galena-barite deposits probably formed in an incipient island-arc environment near a continental margin, containing magmas of keratophyric and andesitic composition, where metal-laden hydrothermal fluids discharged into a deep (?) water, low-energy environment. Later intense deformation, associated with plate docking and thrusting, disrupted and partly remobilized and stratiform deposits.

Alaska↗

USGS1993

Environment of deposition of CaCO3 in Elk Lake, Minnesota

Elk Lake is near the present forest-prairie border in northwestern Minnesota, and is also located on the boundary between hard-water lakes that are typical of once-glaciated parts of the north-central United States and more saline prairie lakes of western Minnesota and the Dakotas. The sediments of the prairie lakes just west of Elk Lake are unusual in that they commonly contain high-Mg calcite and dolomite in addition to low-Mg calcite, which is the dominant carbonate mineral in most marl lakes. During the mid-Holocene dry period, prairie conditions expanded eastward into the forested regions of Minnesota. Variations in types and abundances of carbonate minerals in the Holocene sediments of Elk Lake recorded this climatic change. Studies of primary productivity, carbonate saturation, water chemistry, and sediment-trap samples show that low-Mg calcite precipitates during the summer, triggered by algal photosynthesis. The epilimnion of Elk Lake is always oversaturated with calcite, and the degree of oversaturation increases progressively during the summer. The pH of the epilimnion increases from <8.0 after spring overturn to almost 9.0 in late summer in response to photosynthetic removal of CO 2 during the summer months. The rate of calcium depletion from the epilimnion is proportional to the increase in pH and the rate of photosynthetic carbon fixation. Today the only carbonate minerals that are accumulating in the sediments of Elk Lake are low-Mg calcite and manganese carbonate (rhodochrosite). Rhodochrosite, and probably manganese oxyhydroxide, precipitates when manganese-rich anoxic bottom waters come in contact with carbonate-rich oxic surface waters. During the arid mid-Holocene prairie period, however, low-Mg calcite, dolomite, aragonite, and rhodochrosite all accumulated in the sediments of Elk Lake. Dolomite formed in Elk Lake during this period in response to a higher Mg:Ca ratio in the water, just as it is forming today in lakes of the prairie regions of western Minnesota. The coincident occurrence of aragonite and biological indicators of high salinity suggests that the salinity of Elk Lake and the Mg:Ca ratio were higher than in any of the present prairie lakes of western Minnesota.

Minnesota↗

USGS1998

Chemical weathering in a tropical watershed, Luquillo Mountains, Puerto Rico: I. Long-term versus short-term weathering fluxes

The pristine Rio Icacos watershed in the Luquillo Mountains in eastern Puerto Rico has the fastest documented weathering rate of silicate rocks on the Earth's surface. A regolith propagation rate of 58 m Ma-1 calculated from iso-volumetric saprolite formation from quartz diorite, is comparable to the estimated denudation rate (25-50 Ma-1) but is an order of magnitude faster than the global average weathering rate (6 Ma-1). Weathering occurs in two distinct environments; plagioclase and hornblende react at the saprock interface and biotite and quartz weather in the overlying thick saprolitic regolith. These environments produce distinctly different water chemistries, with K, Mg, and Si increasing linearly with depth in saprolite porewaters and with stream waters dominated by Ca, Na, and Si. Such differences are atypical of less intense weathering in temperate watersheds. Porewater chemistry in the shallow regolith is controlled by closed-system recycling of inorganic nutrients such as K. Long-term elemental fluxes through the regolith (e.g., Si = 1.7 ?? 10-8 moles m-2 s-1) are calculated from mass losses based on changes in porosity and chemistry between the regolith and bedrock and from the age of the regolith surface (200 Ma). Mass losses attributed to solute fluxes are determined using a step-wise infiltration model which calculates mineral inputs to the shallow and deep saprolite porewaters and to stream water. Pressure heads decrease with depth in the shallow regolith (-2.03 m H2O m-1), indicating that both increasing capillary tension and graviometric potential control porewater infiltration. Interpolation of experimental hydraulic conductivities produces an infiltration rate of 1 m yr-1 at average field moisture saturation which is comparable with LiBr tracer tests and with base discharge from the watershed. Short term weathering fluxes calculated from solute chemistries and infiltration rates (e.g., Si = 1.4 ?? 10-8 moles m-2 s-1) are compared to watershed flux rates (e.g., Si = 2.7 ?? 10-8 moles m-2 s-1). Consistency between three independently determined sets of weathering fluxes imply that possible changes in precipitation, temperature, and vegetation over the last several hundred thousand years have not significantly impacted weathering rates in the Luquillo Mountains of Puerto Rico. This has important ramifications for tropical environments and global climate change. Copyright ?? 1998 Elsevier Science Ltd.

Geochimica et Cosmochimica Acta↗

USGS2005

Characterization of waste rock associated with acid drainage at the Penn Mine, California, by ground-based visible to short-wave infrared reflectance spectroscopy assisted by digital mapping

Prior to remediation at the abandoned Cu-Zn Penn Mine in the Foothills massive sulfide belt of the Sierra Nevada, CA, acid mine drainage (AMD) was created, in part, by the subaerial oxidation of sulfides exposed on several waste piles. To support remediation efforts, a mineralogical study of the waste piles was undertaken by acquiring reflectance spectra (measured in the visible to short-wave infrared range of light (0.35-2.5 ??m) using a portable, digitally integrated pen tablet PC mapping system with differential global positioning system and laser rangefinder support. Analysis of the spectral data made use of a continuum removal and band-shape comparison method, and of reference spectral libraries of end-member minerals and mineral mixtures. Identification of secondary Fe-bearing minerals focused on band matching in the region between 0.43 and 1.3 ??m. Identification of sheet and other silicates was based on band-shape analysis in the region between 1.9 and 2.4 ??m. Analysis of reflectance spectra of characterized rock samples from the mine helped in gauging the spectral response to particle size and mixtures. The resulting mineral maps delineated a pattern of accumulation of secondary Fe minerals, wherein centers of copiapite and jarosite that formed at low pH (<3) were surrounded successively by goethite and hematite, which mark progressive increases in pH. This pattern represents the evolution of acid solutions discharged from the pyritic waste piles and the subsequent accumulation of secondary precipitates by hydrolysis reactions. The results highlight the high capacity of the pyritic waste to release further acid mine drainage into the environment, as well as the effectiveness of the mapping method to detect subtle changes in surface mineralogy and to produce maps useful to agencies responsible for remediating the site. ?? 2004 Elsevier B.V. All rights reserved.

Chemical Geology↗

USGS1988

Use of airborne imaging spectrometer data to map minerals associated with hydrothermally altered rocks in the northern Grapevine Mountains, Nevada, and California

Three flightlines of Airborne Imaging Spectrometer (AIS) data, acquired over the northern Grapevine Mountains, Nevada, and California, were used to map minerals associated with hydrothermally altered rocks. The data were processed to remove vertical striping, normalized using an equal area normalization, and reduced to reflectance relative to an average spectrum derived from the data. An algorithm was developed to automatically calculate the absorption band parameters band position, band depth, and band width for the strongest absorption feature in each pixel. These parameters were mapped into an intensity, hue, saturation (IHS) color system to produce a single color image that summarized the absorption band information, This image was used to map areas of potential alteration based upon the predicted relationships between the color image and mineral absorption band. Individual AIS spectra for these areas were then examined to identify specific minerals. Two types of alteration were mapped with the AIS data. Areas of quartz-sericite-pyrite alteration were identified based upon a strong absorption feature near 2.21 μm, a weak shoulder near 2.25 μm, and a weak absorption band near 2.35 μm caused by sericite (fine-grained muscovite). Areas of argillic alteration were defined based on the presence of montmorillonite, identified by a weak to moderate absorption feature near 2.21 μm and the absence of the 2.35 μm band. Montmorillonite could not be identified in mineral mixtures. Calcite and dolomite were identified based on sharp absorption features near 2.34 and 2.32 μm, respectively. Areas of alteration identified using the AIS data corresponded well with areas mapped using field mapping, field reflectance spectra, and laboratory spectral measurements.

California, Nevada↗

USGS1978

Methods for regional assessment of geothermal resources

A consistent, agreed-upon terminology is prerequisite for geothermal resource assessment. Accordingly, we propose a logical, sequential subdivision of the "geothermal resource base", accepting its definition as all the thermal energy in the earth's crust under a given area, measured from mean annual temperature. That part of the resource base which is shallow enough to be tapped by production drilling is termed the "accessible resource base", and it in turn is divided into "useful" and "residual" components. The useful component (i.e. the thermal energy that could reasonably be extracted at costs competitive with other forms of energy at some specified future time) is termed the "geothermal resource". This in turn is divided into "economic" and "subeconomic" components, based on conditions existing at the time of assessment. In the format of a McKelvey diagram, this logic defines the vertical axis (degree of economic feasibility). The horizontal axis (degree of geologic assurance) contains "identified" and "undiscovered" components. "Reserve" is then designated as the identified economic resource. All categories should be expressed in units of thermal energy, with resource and reserve figures calculated at wellhead, prior to the inevitable large losses inherent in any practical thermal use or in conversion to electricity. Methods for assessing geothermal resources can be grouped into 4 classes: (a) surface thermal flux, (b) volume, (c) planar fracture and (d) magmatic heat budget. The volume method appears to be most useful because (1) it is applicable to virtually any geologic environment, (2) the required parameters can in Sprinciple be measured or estimated, (3) the inevitable errors are in part compensated and (4) the major uncertainties (recoverability and resupply) are amenable to resolution in the foreseeable future. The major weakness in all the methods rests in the estimation of how much of the accessible resource base can be extracted at some time in the future. In a manner similar to mineral and fuel assessment, this recoverability is expressed as a "recovery factor". For an ideally permeable hot-water system, the recovery factor may be as much as 50% and seems to be independent of temperature. It must decrease as effective porosity (??e) decreases, but the relation between the two is little more than a guess. On the other hand, for favorable systems like Larderello that produce steam by a mechanism of intergranular vaporization, the recovery factor is probably around 15-20%, decreasing to zero at an effective porosity of zero. According to the anlysis of Bodvarsson (1974), it increases with decreasing reservoir temperature, and as pointed out by Nathenson (1975a) is limited at low temperatures by the need to have sufficient reservoir pressure for extraction and use. The extent to which a geothermal reservoir can be resupplied with heat during "industrial" times of 10-100 yr can be evaluated using simple analytical models. The results, combined with gravity and levelling data of Hunt (1977) for Wairakei and Isherwood (1977) for The Geysers, confirm earlier conclusions by Ramey (1970) and Nathenson (1975a) that resupply to reservoirs producing only steam can be neglected, and the conclusion of Nathenson (1975a) that it may be significant for hot-water systems of high natural discharge. Major subjects that demand continuing investigation include: 1. 1. Determination of recovery factors as functions of temperature and effective porosity, particularly for hot-water systems. 2. 2. Evaluation of fluid recharge and heat resupply by repetitive gravity, levelling and underground temperature surveys in producing geothermal fields. 3. 3. Analysis of the extent to which a recovery factor can be enhanced by stimulation and by use of confined circulation loops. ?? 1979.

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