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D. L. Naftz

Publications and source records attributed to D. L. Naftz.

At least 19 recordsLinked to original sources
USGS2014

Quantity and quality of groundwater discharge in a hypersaline lake environment

Geophysical and geochemical surveys were conducted to understand groundwater discharge to Great Salt Lake (GSL) and assess the potential significance of groundwater discharge as a source of selenium (Se). Continuous resistivity profiling (CRP) focusing below the sediment/water interface and fiber-optic distributed temperature sensing (FO-DTS) surveys were conducted along the south shore of GSL. FO-DTS surveys identified persistent cold-water temperature anomalies at 10 separate locations. Seepage measurements were conducted at 17 sites (mean seepage rate = 0.8 cm/day). High resistivity anomalies identified by the CRP survey were likely a mirabilite (Na 2 SO 4 ·10H 2 O) salt layer acting as a semi-confining layer for the shallow groundwater below the south shore of the lake. Positive seepage rates measured along the near-shore areas of GSL indicate that a ∼1-m thick oolitic sand overlying the mirabilite layer is likely acting as a shallow, unconfined aquifer. Using the average seepage rate of 0.8 cm/day over an area of 1.6 km 2 , an annual Se mass loading to GSL of 23.5 kg was estimated. Determination of R/Ra values (calculated 3 He/ 4 He ratio over the present-day atmospheric 3 He/ 4 He ratio) <1 and tritium activities of 1.2–2.0 tritium units in groundwater within and below the mirabilite layer indicates a convergence of regional and local groundwater flow paths discharging into GSL. Groundwater within and below the mirabilite layer obtains its high sulfate salinity from the dissolution of mirabilite. The δ 34 S and δ 18 O isotopic values in samples of dissolved sulfate from the shallow groundwater below the mirabilite are almost identical to the isotopic signature of the mirabilite core material. The saturation index calculated for groundwater samples using PHREEQC indicates the water is at equilibrium with mirabilite. Water samples collected from GSL immediately off shore contained Se concentrations that were 3–4 times higher than other sampling sites >25 km offshore from the study site and may be originating from less saline groundwater seeps mixing with the more saline water from GSL. Additional evidence for mixing with near shore seeps is found in the δD and δ 18 O isotopic values and Br:Cl ratios. Geochemical modeling for a water sample collected in the vicinity of the study area indicates that under chemically reducing conditions, arsenic- (As) bearing minerals could dissolve while Se-bearing minerals will likely precipitate out of solution, possibly explaining why the shallow groundwater below and within the mirabilite salt layer contains low concentrations of Se (0.9–2.3 μg/L).

Utah↗
USGS2013

Ice thickness, ablation, and other glaciological measurements on Upper Fremont Glacier, Wyoming

Glaciological investigations of the Upper Fremont Glacier in the Wind River Range of Wyoming were conducted during 1990–1991. The glaciological data will provide baseline information for monitoring future changes to the glacier and support ongoing research utilizing glacial - ice -core composition to reconstruct paleoenvironmental records. Ice thickness , determined by radio-echo sounding, ranged from 60 to 172 m in the upper half of the glacier . Radio-echo sounding of ice thickness at one point was confirmed by drilling 159.7 m to bedrock. The difference between radio-echo sounding depth and measured drilling depth was about 4 m. Annual ablation (including snow, firn, and ice ) measured for the 1990–1991 period averaged about 0.93 m/a. Densification proceeds rapidly on Upper Fremont Glacier . Measured densities in the near-surface parts of the glacier ranged from 4.4 x 10 5 g/m 3 at the surface to larger than 8.5 x 10 5 g/m 3 at depths exceeding 14 m. Surface ice velocity and direction were monitored from July 1990 to August 1991. Ice velocity decreased in a downslope direction. The largest measured velocity was about 3.1 m/a and the smallest was 0.8 m/a. The yearly mean air temperature of the study site during the period from July 11, 1990 to July 10, 1991 was -6.9°. Borehole temperatures from 10-m depths are 0 ± 0.4°. The warmer borehole temperatures relative to the yearly mean air temperature may be caused by the latent heat of freezing, as meltwater from the surface percolates into the glacier and refreezes.

Wyoming↗
USGS2011

An equation of state for hypersaline water in Great Salt Lake, Utah, USA

Great Salt Lake (GSL) is one of the largest and most saline lakes in the world. In order to accurately model limnological processes in GSL, hydrodynamic calculations require the precise estimation of water density ( ρ ) under a variety of environmental conditions. An equation of state was developed with water samples collected from GSL to estimate density as a function of salinity and water temperature. The ρ of water samples from the south arm of GSL was measured as a function of temperature ranging from 278 to 323 degrees Kelvin ( o K) and conductivity salinities ranging from 23 to 182 g L −1 using an Anton Paar density meter. These results have been used to develop the following equation of state for GSL (σ = ± 0.32 kg m −3 ): ρ − ρ 0 = 184 .0 10 6 2 + 1 .0 4 70 8 ∗ S − 1. 2 10 6 1 ∗ T + 3 . 1 4 7 2 1 E − 4 ∗ S 2 + 0.00 1 9 9 T 2 − 0.00 1 1 2 ∗ S ∗ T , where ρ 0 is the density of pure water in kg m −3 , S is conductivity salinity g L −1 , and T is water temperature in degrees Kelvin.

Utah↗
USGS2009

Estimating selenium removal by sedimentation from the Great Salt Lake, Utah

The mass of Se deposited annually to sediment in the Great Salt Lake (GSL) was estimated to determine the significance of sedimentation as a permanent Se removal mechanism. Lake sediment cores were used to qualitatively delineate sedimentation regions (very high to very low), estimate mass accumulation rates (MARs) and determine sediment Se concentrations. Sedimentation regions were defined by comparison of isopach contours of Holocene sediment thicknesses to linear sedimentation rates determined via analysis of 210 Pb, 226 Ra, 7 Be and 137 Cs activity in 20 short cores (<5 cm), yielding quantifiable results in 13 cores. MARs were developed via analysis of the same radioisotopes in eight long cores (>10 cm). These MARs in the upper 1-2 cm of each long core ranged from 0.019 to 0.105 g sed /cm 2 /a. Surface sediment Se concentrations in the upper 1 or 2 cm of each long core ranged from 0.79 to 2.47 mg/kg. Representative MARs and Se concentrations were used to develop mean annual Se removal by sedimentation in the corresponding sedimentation region. The spatially integrated Se sedimentation rate was estimated to be 624 kg/a within a range of uncertainty between 285 and 960 kg/a. Comparison to annual Se loading and other potential removal processes suggests burial by sedimentation is not the primary removal process for Se from the GSL. ?? 2009 Elsevier Ltd.

Applied Geochemistry↗
USGS2009

Size and elemental distributions of nano- to micro-particulates in the geochemically-stratified Great Salt Lake

The characterization of trace elements in terms of their apportionment among dissolved, macromolecular, nano- and micro-particulate phases in the water column of the Great Salt Lake carries implications for the potential entry of toxins into the food web of the lake. Samples from the anoxic deep and oxic shallow brine layers of the lake were fractionated using asymmetric flow field-flow fractionation (AF4). The associated trace elements were measured via online collision cell inductively-coupled plasma mass spectrometry (CC-ICP-MS). Results showed that of the total (dissolved + particulate) trace element mass, the percent associated with particulates varied from negligible (e.g. Sb), to greater than 50% (e.g. Al, Fe, Pb). Elements such as Cu, Zn, Mn, Co, Au, Hg, and U were associated with nanoparticles, as well as being present as dissolved species. Particulate-associated trace elements were predominantly associated with particulates larger than 450 nm in size. Among the smaller nanoparticulates (<450 nm), some trace elements (Ni, Zn, Au and Pb) showed higher percent mass (associated with nanoparticles) in the 0.9-7.5 nm size range relative to the 10-250 nm size range. The apparent nanoparticle size distributions were similar between the two brine layers; whereas, important differences in elemental associations to nanoparticles were discerned between the two layers. Elements such as Zn, Cu, Pb and Mo showed increasing signal intensities from oxic shallow to anoxic deep brine, suggesting the formation of sulfide nanoparticles, although this may also reflect association with dissolved organic matter. Aluminum and Fe showed greatly increased concentration with depth and equivalent size distributions that differed from those of Zn, Cu, Pb and Mo. Other elements (e.g. Mn, Ni, and Co) showed no significant change in signal intensity with depth. Arsenic was associated with <2 nm nanoparticles, and showed no increase in concentration with depth, possibly indicating dissolved arsenite. Mercury was associated with <2 nm nanoparticles, and showed greatly increased concentration with depth, possibly indicating association with dissolved organic matter. ?? 2009 Elsevier Ltd.

Applied Geochemistry↗
USGS2009

Selenium mass balance in the Great Salt Lake, Utah

A mass balance for Se in the south arm of the Great Salt Lake was developed for September 2006 to August 2007 of monitoring for Se loads and removal flows. The combined removal flows (sedimentation and volatilization) totaled to a geometric mean value of 2079??kg Se/yr, with the estimated low value being 1255??kg Se/yr, and an estimated high value of 3143??kg Se/yr at the 68% confidence level. The total (particulates + dissolved) loads (via runoff) were about 1560??kg Se/yr, for which the error is expected to be ?? 15% for the measured loads. Comparison of volatilization to sedimentation flux demonstrates that volatilization rather than sedimentation is likely the major mechanism of selenium removal from the Great Salt Lake. The measured loss flows balance (within the range of uncertainties), and possibly surpass, the measured annual loads. Concentration histories were modeled using a simple mass balance, which indicated that no significant change in Se concentration was expected during the period of study. Surprisingly, the measured total Se concentration increased during the period of the study, indicating that the removal processes operate at their low estimated rates, and/or there are unmeasured selenium loads entering the lake. The selenium concentration trajectories were compared to those of other trace metals to assess the significance of selenium concentration trends. ?? 2008 Elsevier B.V.

Science of the Total Environment↗
USGS2009

Selenium and trace element mobility affected by periodic displacement of stratification in the Great Salt Lake, Utah

The Great Salt Lake (GSL) is a unique ecosystem in which trace element activity cannot be characterized by standard geochemical parameters due to the high salinity. Movement of selenium and other trace elements present in the lake bed sediments of GSL may occur due to periodic stratification displacement events or lake bed exposure. The water column of GSL is complicated by the presence of a chemocline persistent over annual to decadal time scales. The water below the chemocline is referred to as the deep brine layer (DBL), has a high salinity (16.5 to 22.9%) and is anoxic. The upper brine layer (UBL) resides above the chemocline, has lower salinity (12.6 to 14.7%) and is oxic. Displacement of the DBL may involve trace element movement within the water column due to changes in redox potential. Evidence of stratification displacement in the water column has been observed at two fixed stations on the lake by monitoring vertical water temperature profiles with horizontal and vertical velocity profiles. Stratification displacement events occur over periods of 12 to 24 h and are associated with strong wind events that can produce seiches within the water column. In addition to displacement events, the DBL shrinks and expands in response to changes in the lake surface area over a period of months. Laboratory tests simulating the observed sediment re-suspension were conducted over daily, weekly and monthly time scales to understand the effect of placing anoxic bottom sediments in contact with oxic water, and the associated effect of trace element desorption and (or) dissolution. Results from the laboratory simulations indicate that a small percentage (1%) of selenium associated with anoxic bottom sediments is periodically solubilized into the UBL where it potentially can be incorporated into the biota utilizing the oxic part of GSL.

Science of the Total Environment↗
USGS2008

Volatile selenium flux from the great Salt Lake, Utah

The removal mechanisms that govern Se concentrations in the Great Salt Lake are unknown despite this terminal lake being an avian habitat of hemispheric importance. However, the volatilization flux of Se from the Great Salt Lake has not been previously measured due to challenges of analysis in this hypersaline environment This paper presents results from recent field studies examining the spatial distribution of dissolved volatile Se (areally and with depth) in the south arm (main body) of the Great Salt Lake. The analyses involved collection of dissolved volatile Se in a cryofocusing trap system via sparging with helium. The cryotrapped volatile Se was digested with nitric acid and analyzed by inductively coupled plasma mass spectrometry (ICP-MS). Results show concentrations of dissolved volatile Se that increase with depth in the shallow brine, suggesting that phytoplankton in the open waters and bioherms in shallow sites (<4 m in depth) may be responsible for volatile Se production. Volatile Se flux to the atmosphere was determined using mass transport models corrected to simulate the highly saline environment of the south arm of the Great Salt Lake. The estimated annual flux of volatile Se was 1455 kg/year within a range from 560 to 3780 kg Se/year for the 95% confidence interval and from 970 to 2180 kg Se/year within the 68% confidence interval. ?? 2009 American Chemical Society.

Environmental Science & Technology↗
USGS2007

Salinity increases in the navajo aquifer in southeastern Utah

Salinity increases in water in some parts of the Navajo aquifer in southeastern Utah have been documented previously. The purpose of this paper is to use bromide, iodide, and chloride concentrations and del oxygen-18 and deuterium values in water from the study area to determine if oil-field brines (OFB) could be the source of increased salinity. Mixing-model results indicate that the bromide-to-chloride X 10,000 weight ratio characteristic of OFB in and outside the study area could not be causing the bromide depletion with increasing salinity in the Navajo aquifer. Mixing-model results indicate that a mixture of one percent OFB with 99 percent Navajo aquifer water would more than double the bromide-to-chloride weight ratio, instead of the observed decrease in the weight ratio with increasing chloride concentration. The trend of the mixing line representing the isotopically enriched samples from the Navajo aquifer does not indicate OFB as the source of isotopically enriched water; however, the simulated isotopic composition of injection water could be a salinity source. The lighter isotopic composition of OFB samples from the Aneth, Ratherford, White Mesa Unit, and McElmo Creek injection sites relative to the Ismay site is a result of continued recycling of injection water mixed with various proportions of isotopically lighter make-up water from the alluvial aquifer along the San Juan River. A mixing model using the isotopic composition of the simulated injection water suggests that enriched samples from the Navajo aquifer are composed of 36 to 75 percent of the simulated injection water. However, chloride concentrations predicted by the isotopic mixing model are up to 13.4 times larger than the measured chloride concentrations in isotopically enriched samples from the Navajo aquifer, indicating that injection water is not the source of increased salinity. Geochemical data consistently show that OFB and associated injection water from the Greater Aneth Oil Field are not the source of salinity increases in the Navajo aquifer.

Water Resources Bulletin↗
USGS2006

Processes affecting transport of uranium in a suboxic aquifer

At the Naturita site in Colorado, USA, groundwaters were sampled and analyzed for chemical composition and by culture and culture-independent microbiological techniques. In addition, sediments were extracted with a dilute sodium carbonate solution to determine quantities of labile uranium within the sediments. Samples from the upgradient portion of the contaminated aquifer , where very little dissolved Fe(II) is found in the groundwater, have uranium content that is controlled by U(VI) adsorption and few metal-reducing bacteria are observed. In the extreme downgradient portion of the aquifer, where dissolved Fe(II) is observed, uranium content of the sediments includes significant quantities of reduced U(IV) and diverse populations of Fe(III)-reducing bacteria were present in the subsurface with the potential of reducing U(VI) to U(IV).

Physics and Chemistry of the Earth↗
USGS2006

Hydrology and water quality in the Green River and surrounding agricultural areas near Green River in Emery and Grand Counties, Utah, 2004-05

Water from the Colorado River and its tributaries is used for municipal and industrial purposes by about 27 million people and irrigates nearly 4 million acres of land in the Western United States. Water users in the Upper Colorado River Basin consume water from the Colorado River and its tributaries, reducing the amount of water in the river. In addition, application of water to agricultural land within the basin in excess of crop needs can increase the transport of dissolved solids to the river. As a result, dissolved-solids concentrations in the Colorado River have increased, affecting downstream water users. During 2004-05, the U.S. Geological Survey, in cooperation with the Natural Resources Conservation Service, investigated the occurrence and distribution of dissolved solids in water from the agricultural areas near Green River, Utah, and in the adjacent reach of the Green River, a principle tributary of the Colorado River. The flow-weighted concentration of dissolved solids diverted from the Green River for irrigation during 2004 and 2005 was 357 milligrams per liter and the mean concentration of water collected from seeps and drains where water was returning to the river during low-flow conditions was 4,170 milligrams per liter. The dissolved-solids concentration in water from the shallow part of the ground-water system ranged from 687 to 55,900 milligrams per liter. Measurable amounts of dissolved solids discharging to the Green River are present almost exclusively along the river banks or near the mouths of dry washes that bisect the agricultural areas. The median dissolved-solids load in discharge from the 17 drains and seeps visited during the study was 0.35 ton per day. Seasonal estimates of the dissolved-solids load discharging from the study area ranged from 2,800 tons in the winter to 6,400 tons in the spring. The estimate of dissolved solids discharging from the study area annually is 15,700 tons. Water samples collected from selected sites within the Green River agricultural areas were analyzed for naturally occurring isotopes of strontium and boron, which can be useful for differentiating dissolved-solids sources. Substantial variations in the delta strontium-87 and delta boron-11 values among the sites were measured. Canal and river samples had relatively low concentrations of strontium and the most positive (heavier) isotopic ratios, while drains and seeps had a wide range of strontium concentrations and isotopic ratios that generally were less positive (lighter). Further study of the variation in strontium and boron concentrations and isotope ratios may provide a means to distinguish end members and discern processes affecting dissolved solids within the Green River study area; however, the results from isotope data collected during this study are inconclusive. Flow and seepage losses were estimated for the three main canals in the study area for May 2 to October 4 in any given year. This period coincides with the frost-free period in the Green River area. Estimated diversion from the Green River into the Thayn, East Side, and Green River Canals is 6,600, 6,070, and 19,900 acre-feet, respectively. The estimated seepage loss to ground water from the Thayn, East Side, and Green River Canals during the same period is 1,550, 1,460, and 4,710 acre-feet, respectively.

Utah↗
USGS2005

Selenium mobilization during a flood experiment in a contaminated wetland: Stewart Lake Waterfowl Management Area, Utah

Constructed and natural wetlands can accumulate elevated levels of Se; however, few data are available on cost-effective methods for remobilization and removal of Se from these areas. A field experiment was conducted to assess the effectiveness of flooding on the removal of Se from dry surface sediments. The 83-m2 flood-experiment plot contained 10 monitoring wells, a water-quality minimonitor (continuous measurement of pH, specific conductance, water temperature, and dissolved O2), a down-hole Br electrode, and 2 pressure transducers. Flooding was initiated on August 27, 2002, and a Br tracer was added to water delivered through a pipeline to the flood plot during the first 1.2 h. Standing water depth in the flood plot was maintained at 0.3 m through September 1, 2002. The Br tracer data indicate a dual porosity system that includes fracture (mud cracks) and matrix flow components. Mean vertical water velocities for the matrix flow component were estimated to range from 0.002 to 0.012 m/h. Dissolved (less than 0.45 ??m) Se increased from pre-flood concentrations of less than 10 ??g/L to greater than 800 ??g/L during flooding in samples from deep (2.0 m below land surface) ground water. Selenium concentrations exceeded 5500 ??g/L in samples from shallow (0.8 m below land surface) ground water. Ratios of Se to Br in water samples indicate that Se moved conservatively during the experiment and was derived from leaching of near-surface sediments. Cumulative Se flux to the deep ground water during the experiment ranged from 9.0 to 170 mg/m2. Pre- and post-flood surface soil sampling indicated a mean Se flux of 720 mg/m2 through the top 15 cm of soil. Ground-water samples collected 8 months after termination of the flood experiment contained Se concentrations of less than 20 ??g/L. The minimonitor data indicate a rapid return to chemically reducing conditions in the deep ground water, limiting the mobility of the Se dissolved in the water pulse introduced during the flood experiment. Ratios of Se to Br in deep ground-water samples collected 8 months after the experiment confirmed the removal of Se from the aqueous phase. Based on the median Se flux rate estimated during the experiment of 0.65 mg/h/m2 (n = 52), 7 flooding cycles would be required to meet the 4 ??g/g remediation goal in surface soils from the SLWMA wetland.

Applied Geochemistry↗
USGS2000

Chlorine-36 and cesium-137 in ice-core samples from mid-latitude glacial sites in the Northern Hemisphere

Chlorine-36 (36Cl) concentrations, 36Cl/Cl ratios, and 36Cl fluxes in ice-core samples collected from the Upper Fremont Glacier (UFG) in the Wind River Mountain Range, Wyoming, United States and the Nangpai Gosum Glacier (NGG) in the Himalayan Mountains, Nepal, were determined and compared with published results from the Dye-3 ice-core drilling site on the Greenland Ice Sheet. Cesium-137 (137Cs) concentrations in the NGG also were determined. The background fluxes for 36Cl for each glacial site were similar: (1.6??0.3)??10-2 atoms/cm2 s for the UFG samples, (0.7??0.1)??10-2 atoms/cm2 s for the NGG samples, and (0.4??0.1)??10-2 atoms/cm2 s for the Dye-3 samples. The 36Cl fluxes in ice that was deposited as snow during peak atmospheric nuclear weapon test (1957-1958) were (33??1)??10-2 atoms/cm2 s for the UFG site, (291??3)??10-2 atoms/cm2 s for the NGG site, and (124??5)??10-2 atoms/ cm2 s for the Dye-3 site. A weapon test period 137Cs concentration of 0.79??0.05 Bq/kg in the NGG ice core also was detected in the same section of ice that contained the largest 36Cl concentration. ?? 2000 Elsevier Science B.V. All rights reserved.

Nuclear Instruments and Methods in Physics Researc↗
USGS2000

USGS research on three mid-latitude glaciers

Low- and mid-latitude regions of the earth are home to 80 to 90 percent of the world's population. Because of this, the U.S. Geological Survey (USGS) is conducting a research program to study the geochemistry of precipitation, snow, ice, and runoff samples from mid-latitude glaciers in Kyrghyzstan, Nepal, and the United States, Areas of research, such as ground-water studies, reconstructing paleoclimate records, describing anthropogenic input of chemicals to the environment, and modeling global climate, are important to the well being of the worlds' population and can be supplemented by the collection and chemical analysis of snow and ice cores. Nearly all the constituents that compose snow and ice-core samples contribute vital information, whether it be the microbial communities that flourish in snow, radionuclides present in various amounts in all the samples, or location-specific deposits of mercury and nitrate. This work is hastened by the fact that mid-latitude glaciers, and the information preserved in them, are rapidly disappearing as a result of global warming. Research collaboration for this project includes 12 national and 7 international universities, and 4 government agencies. Funding is provided by the National Science Foundation, the U.S. Department of Energy, and the USGS.

Conference Paper↗
USGS1997

Using δ 87 Sr values to identify sources of salinity to a freshwater aquifer, Greater Aneth Oil Field, Utah, USA

Salinity increases in water from the freshwater Navajo aquifer in the Aneth area have been documented in recent years. Previous studies during the 1980s in the Aneth area suggested that brines associated with oil production and their subsequent re-injection were the probable source of salinity in the Navajo aquifer. Differences in the delta strontium-87 (&delta; 87 Sr) composition of ground-water samples from southeastern Utah were used to determine if oil-field brine or water from the upper Paleozoic aquifer is a plausible source of salinity to the Navajo aquifer. The &delta; 87 Sr values of the oil-field brine samples (mean = &minus;0.95%, range = &minus;1.06 to &minus;0.79%, n = 5) are substantially more negative than the values in water samples from wells completed in the Navajo aquifer (mean = 0.73, range = &minus;0.85 to 2.02%, n = 48), indicating that oil-field brine is not a source of salinity. The &delta; 87 Sr values in water samples from wells completed in the upper Paleozoic aquifer (mean = 0.801% range = 0.34 to 1.10%, n = 4) are similar to the mean isotopic composition of the more saline water from the Navajo aquifer. The &delta; 87 Sr values in water from the Navajo aquifer confirm that two distinct flow areas are present. Mixing models using the &delta; 87 Sr values and Sr concentrations of non-saline water from the Navajo aquifer and saline water from the upper Paleozoic aquifer indicate that water from the upper Paleozoic aquifer is a plausible source of saline water to the Navajo aquifer. Most Navajo aquifer wells that contain water with a &delta; 87 Sr signature similar to water from the upper Paleozoic aquifer are located within or adjacent to an area where the hydraulic gradient is favorable for upward movement of water from the upper Paleozoic aquifer into the Navajo aquifer.

Chemical Geology↗
USGS1996

Pattern recognition analysis and classification modeling of selenium-producing areas

Established chemometric and geochemical techniques were applied to water quality data from 23 National Irrigation Water Quality Program (NIWQP) study areas in the Western United States. These techniques were applied to the NIWQP data set to identify common geochemical processes responsible for mobilization of selenium and to develop a classification model that uses major-ion concentrations to identify areas that contain elevated selenium concentrations in water that could pose a hazard to water fowl. Pattern recognition modeling of the simple-salt data computed with the SNORM geochemical program indicate three principal components that explain 95% of the total variance. A three-dimensional plot of PC 1, 2 and 3 scores shows three distinct clusters that correspond to distinct hydrochemical facies denoted as facies 1, 2 and 3. Facies 1 samples are distinguished by water samples without the CaCO 3 simple salt and elevated concentrations of NaCl, CaSO 4 , MgSO 4 and Na 2 SO 4 simple salts relative to water samples in facies 2 and 3. Water samples in facies 2 are distinguished from facies 1 by the absence of the MgSO 4 simple salt and the presence of the CaCO 3 simple salt. Water samples in facies 3 are similar to samples in facies 2, with the absence of both MgSO 4 and CaSO 4 simple salts. Water samples in facies 1 have the largest selenium concentration (10 μg l −1 ), compared to a median concentration of 2·0 μg l −1 and less than 1·0 μg l −1 for samples in facies 2 and 3. A classification model using the soft independent modeling by class analogy (SIMCA) algorithm was constructed with data from the NIWQP study areas. The classification model was successful in identifying water samples with a selenium concentration that is hazardous to some species of water-fowl from a test data set comprised of 2,060 water samples from throughout Utah and Wyoming. Application of chemometric and geochemical techniques during data synthesis analysis of multivariate environmental databases from other national-scale environmental programs such as the NIWQP could also provide useful insights for addressing ‘real world’ environmental problems.

Journal of Chemometrics↗
USGS1996

Little Ice Age evidence from a south-central North American ice core, U.S.A.

In the past, ice-core records from mid-latitude glaciers in alpine areas of the continental United States were considered to be poor candidates for paleoclimate records because of the influence of meltwater on isotopic stratigraphy. To evaluate the existence of reliable paleoclimatic records, a 160-m ice core, containing about 250 yr of record was obtained from Upper Fremont Glacier, at an altitude of 4000 m in the Wind River Range of south-central North America. The δ 18 O (SMOW) profile from the core shows a -0.95‰ shift to lighter values in the interval from 101.8 to 150 m below the surface, corresponding to the latter part of the Little Ice Age (LIA). Numerous high-amplitude oscillations in the section of the core from 101.8 to 150 m cannot be explained by site-specific lateral variability and probably reflect increased seasonality or better preservation of annual signals as a result of prolonged cooler temperatures that existed in this alpine setting. An abrupt decrease in these large amplitude oscillations at the 101.8-m depth suggests a sudden termination of this period of lower temperatures which generally coincides with the termination of the LIA. Three common features in the δ18O profiles between Upper Fremont Glacier and the better dated Quelccaya Ice Cap cores indicate a global paleoclimate linkage, further supporting the first documented occurrence of the LIA in an ice-core record from a temperate glacier in south-central North America.

Upper Fremont Glacier, Wind River Range↗