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  • 1
    ISSN: 1745-6584
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Geosciences
    Notes: Concentrations of 40 trace elements and other constituents in ground water from springs in Death Valley National Park were measured to investigate whether trace element composition of the ground water can be related to the aquifer materials. Samples from these springs were analyzed by inductively coupled plasma-mass spectrometry (ICP-MS) for the trace elements and by ion chromatography (IC) for the major anions. A Principal Component Analysis was performed on the data set. Surprise and Scotty's Springs formed one group; Texas, Nevares, and Travertine Springs formed another group; and Mesquite Springs did not group with any of the others. Scotty's and Surprise Spring issued from volcanic rocks; Texas, Nevares, and Travertine discharge from carbonate rocks; and Mesquite Spring is located in alluvial basin-fill deposits. The first three components in each Principal Component Analysis accounted for approximately 95% of the variance in the data set. The Principal Component Analysis suggests that ground water inherits its trace element composition from the rocks or aquifer material with which it has interacted and may be used for the purpose of identifying ground-water movement and source.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1745-6584
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Geosciences
    Notes: The rare earth element (REE) signature of ground waters from both felsic volcanic rocks on the Nevada Test Site and from the regional Paleozoic carbonate aquifer of southern Nevada resemble the REE signature of the rocks through which they flow. Moreover, the REE signatures of Ash Meadows ground waters are similar to those of springs in the Furnace Creek region of Death Valley but different from shallow ground waters from predominantly tuffaceous alluvial deposits in the Amargosa Desert, perched ground waters from felsic volcanic rocks, and ground waters that have only flowed through the regional Paleozoic carbonate aquifer. The similar REE patterns of Ash Meadows and Furnace Creek ground waters support previous investigations that suggested ground waters discharging from the Furnace Creek springs are similar to the ground waters emerging from the Ash Meadows springs. The REE patterns indicate that the contribution of ground water from the Amargosa Desert to the Furnace Creek springs is of minor importance. Our REE analyses along with previous stable isotope, ground-water potentiometric surface relationships, and geologic structure analyses support ground-water flow from east to west in the fractured and faulted carbonate rocks beneath Ash Meadows, the Amargosa Desert, and the southern end of the Funeral Mountains. Our observations are contrary to some previous investigations that identified shallow ground waters from the central and northwestern Amargosa Desert as a substantial component of the ground water that discharges from the Furnace Creek springs.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-0417
    Keywords: paleolimnology ; lake levels ; biogenic silica ; organic matter ; isotopes ; North Dakota
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Geosciences
    Notes: Abstract An 84 cm sediment core collected from the center of Devils Lake, North Dakota, was analyzed at 1-cm intervals for,210Pb,137Cs, sediment conductivity, the concentrations of, biogenic silica, total organic carbon, carbon to nitrogen ratio, and the carbon and nitrogen isotopic composition of the organic fraction. Variations in210Pb activities in the upper 20 centimeters indicate that sediment accumulations rates in Devils Lake are not constant, and that accumulation rates were highest during periods of high lake level. The mean sedimentation accumulation rate was calculated as 0.24 cm−1 yr. The137Cs profile is characterized by near-surface maximum concentrations, possibly the result of redistribution of137Cs during salinity excursions. Biogenic silica is strongly correlated to lake level in Devils Lake. Periods of low lake level (characterized by high sediment conductivity) correspond to low biogenic silica concentrations. The trends in biogenic silica are attributed to variations in diatom productivity in the lake and to variations in sediment accumulation rates. Based on biogenic silica content and the composition of organic matter in the sediment (total organic carbon, carbon:nitrogen ratio and the δ13C and δ15N composition of total organic matter), paleobiologic conditions of Devils Lake during low lake stands were characterized by, (1) decreased primary productivity, (2) decreased input of detrital organic matter, and (3) increased nitrogen availability. During the 350 years of sediment accumulation represented by the 84-cm sediment core Devils Lake has experienced two periods of sustained high lake level; one between about 130 and 170 years ago (1820 to 1860 A.D.) and the second between 270 and 310 years ago (1680 to 1720 A.D.). Devils Lake experienced a period of intense drying about 260 years ago (1720 A.D.).
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-1421
    Keywords: arsenic ; phosphate ; oxyanions ; eastern Sierra Nevada rivers ; surface waters ; Lake Tahoe ; Pyramid Lake ; Walker Lake ; closed-basin lakes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Water samples were collected from the Truckee River-Pyramid Lake system, the Walker River-Walker Lake system, and the Carson River, all located in eastern California and western Nevada, U.S.A., at three different times (i.e., summer 1991, spring 1992, and autumn 1992) over a two year period. The concentrations of As, Na, Cl, ΣPO4, and pH were measured in these river samples and the associated terminal lakes. Arsenic values ranged from below 13 nmol/kg near Truckee, California to 160 nmol/kg at Nixon, Nevada in the Truckee River, from 40 nmol/kg in the headwaters of both West and East Walker Rivers to 270 nmol/kg below Weber Reservoir on the main branch of the Walker River, and from 〈27 nmol/kg to 234 nmol/kg for the lower Carson River system. Arsenic concentrations in Steamboat Creek (0.91 μmol/kg–1.80 μmol/kg) in the Truckee River catchment are above the U.S. EPA drinking water maximum contaminant level of 0.67 μmol/kg, as are the As concentrations in both Pyramid Lake (1.33 μmol/kg–1.57 μmol/kg ) and Walker Lake (13.7 μmol/kg–18.7 μmol/kg). Sources of As for all three rivers include weathering of As-rich rocks and/or regolith and input of high-As geothermal spring waters, both processes primarily, although not exclusively, adding As to the headwater regions of these rivers. Steamboat Hot Springs (29 μmol/kg ≤ As ≤ 54.5 μmol/kg), for example, is identified as a source of As to the Truckee River via Steamboat Creek. The high As concentrations in Pyramid and Walker Lakes are likely due to (1) desorption of arsenate from aquatic particulate matter in these high pH waters (9.0 ≤ pH ≤ 9.5), (2) limited biologic uptake of arsenate, and (3) evaporative concentration of the lake waters. Evaluation of molar ΣPO4}/As ratios of river waters and geothermal spring waters (e.g., Steamboat Hot Springs), indicates that phosphate is substantially enriched in Steamboat Creek as well as the mid to lower reaches of the Walker and Carson Rivers. These regions of each river are dominated by agricultural interests and, additionally, in the case of Steamboat Creek, residential areas and golf courses. Our data strongly imply that phosphate-rich agricultural return flow has likely added P to these streams and, consequently, increased their respective P:As ratios.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1573-1421
    Keywords: rare earth elements ; lakes ; groundwaters ; activity products ; solubility products ; solubility controls ; complexation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Rare earth element (REE) concentrations in alkaline lakes, circumneutral pH groundwaters, and an acidic freshwater lake were determined along with the free carbonate, free phosphate, and free sulfate ion concentrations. These parameters were used to evaluate the saturation state of these waters with respect to REE phosphate and carbonate precipitates. Our activity product estimates indicate that the alkaline lake waters and groundwaters are approximately saturated with respect to the REE phosphate precipitates but are significantly undersaturated with respect to REE carbonate and sulfate precipitates. On the other hand, the acidic lake waters are undersaturated with respect to REE sulfate, carbonate, and phosphate precipitates. Although carbonate complexes tend to dominate the speciation of the REEs in neutral and alkaline waters, our results indicate that REE phosphate precipitates are also important in controlling REE behavior. More specifically, elevated carbonate ion concentrations in neutral to alkaline natural waters tend to enhance dissolved REE concentrations through the formation of stable REE-carbonate complexes whereas phosphate ions tend to lead to the removal of the REEs from solution in these waters by the formation of REE-phosphate salts. Removal of REEs by precipitation as phosphate phases in the acid lake (pH=3.6) is inconsequential, however, due to extremely low [PO 4 3− ] F concentrations (i.e., ∼ 10−23 mol/kg).
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1573-1421
    Keywords: Boron ; eastern Sierra Nevada rivers ; Lake Tahoe ; molybdenum ; oxyanions ; Pyramid Lake ; tungsten ; vanadium ; Walker Lake
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Water samples were collected from 10 locations along the Truckee River system, 14 locations along the Walker River system, and 12 locations along the Carson River, and analyzed for B, Mo, V, W, Na, Cl, and pH. Boron concentrations ranged from approximately 2 μmol/kg in the upper reaches of the Truckee River to almost 1,200 μmol/kg in Pyramid Lake. Molybdenum, V, and W had concentrations in the nanomolal range; Mo varied from a low of about 12 nmol/kg to a high of 3,200 nmol/kg (Walker Lake); V ranged from 9 nmol/kg to approximately 470 nmol/kg; and W varied from a low value around 0.8 nmol/kg (West Walker River) to 1,030 nmol/kg. The high concentrations of these oxyanion-forming trace elements in the rivers reflects (1) the relative stability of these oxyanions (e.g., MoO4 2-, HVO4 2-, WO4 2-, B(OH)3, and/or B(OH)4 -) in the alkaline, well oxygenated river and lake waters, (2) contributions of hydrothermal waters (especially for B), and (3) weathering of rocks/regolith with high concentrations of these elements. In the case of Mo, V, and W, each exhibited relatively conservative behavior in the upper, oxygenated reaches of all three rivers. During the study period the region experienced a prolonged drought such that the lower reaches of each river were typified by no flow or stagnant waters and probably low oxygen and/or anoxic conditions (although not measured). Reductive processes occurring in the low flow to stagnant reaches of each river could have led to removal of Mo, V, and W from solution as coprecipitates with Fe monosulfides, or via sorption to Fe oxides/oxyhydroxides and/or organic matter. Boron, however, exhibited essentially no or minor removal from these rivers, and instead was added to each river via B-rich hydrothermal waters (e.g., Steamboat Creek from Steamboat Hot Springs), or by B-rich groundwaters via base-flow during the extensive drought.
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  • 7
    ISSN: 1573-8868
    Keywords: principal components analysis ; cluster analysis ; population partitioning ; trace element compositions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Mathematics
    Notes: Abstract The origin of groundwater discharging via evapotranspiration and from springs within Oasis Valley, Nevada, is of concern owing to the close proximity of the Nevada Test Site (NTS) and the possible contamination of groundwater as a result of underground nuclear testing. Principal components analysis, cluster analysis, and population partitioning, along with a Geographical Information System, were used to decipher groundwater flow patterns in Oasis Valley, Nevada. These multivariate statistical techniques were applied to the trace element chemistry of groundwater samples collected from 26 springs and wells within Oasis Valley, the NTS, and the Nellis Air Force Range. The results of all statistical analyses showed similar geographical trends in the trace element chemistry of the groundwaters included in this study. Differences are observed between the groundwaters from the NTS and those of Oasis Valley based on the concentrations of the elements Li, Ge, Mo, Rb, Ba, U, and Ru. A concentration gradient is observed from lower concentrations in the NTS to increasing concentrations toward Oasis Valley suggesting groundwater flow in an overall southwestward direction from the NTS. Also, a different trace element signature is observed for the waters collected in the northern and western region of Oasis Valley, suggesting another source of groundwater to this area.
    Type of Medium: Electronic Resource
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