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D. L. Naftz

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

34 records · Page 2Linked to original sources
USGS2000

Chronological refinement of an ice core record at Upper Fremont Glacier in south central North America

The potential to use ice cores from alpine glaciers in the midlatitudes to reconstruct paleoclimatic records has not been widely recognized. Although excellent paleoclimatic records exist for the polar regions, paleoclimatic ice core records are not common from midlatitude locations. An ice core removed from the Upper Fremont Glacier in Wyoming provides evidence for abrupt climate change during the mid-1800s. Volcanic events (Krakatau and Tambora) identified from electrical conductivity measurements (ECM) and isotopic and chemical data from the Upper Fremont Glacier were reexamined to confirm and refine previous chronological estimates of the ice core. At a depth of 152 m the refined age-depth profile shows good agreement (1736 ± 10 A.D.) with the 14C age date (1729 ± 95 A.D.). The δ 18 O profile of the Upper Fremont Glacier (UFG) ice core indicates a change in climate known as the Little Ice Age (LIA). However, the sampling interval for δ 18 O is sufficiently large (20 cm) such that it is difficult to pinpoint the LIA termination on the basis of δ 18 O data alone. Other research has shown that changes in the δ18O variance are generally coincident with changes in ECM variance. The ECM data set contains over 125,000 data points at a resolution of 1 data point per millimeter of ice core. A 999-point running average of the ECM data set and results from f tests indicates that the variance of the ECM data decreases significantly at about 108 m. At this depth, the age-depth profile predicts an age of 1845 A.D. Results indicate the termination of the LIA was abrupt with a major climatic shift to warmer temperatures around 1845 A.D. and continuing to present day. Prediction limits (error bars) calculated for the profile ages are ±10 years (90% confidence level). Thus a conservative estimate for the time taken to complete the LIA climatic shift to present-day climate is about 10 years, suggesting the LIA termination in alpine regions of central North America may have occurred on a relatively short (decadal) timescale. Copyright 2000 by the American Geophysical Union.

Wyoming↗
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 (δ 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 δ 87 Sr values of the oil-field brine samples (mean = −0.95%, range = −1.06 to −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 = −0.85 to 2.02%, n = 48), indicating that oil-field brine is not a source of salinity. The δ 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 δ 87 Sr values in water from the Navajo aquifer confirm that two distinct flow areas are present. Mixing models using the δ 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 δ 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↗
USGS1994

Assessment of spatial variability of major-ion concentrations and del oxygen-18 values in surface snow, Upper Fremont Glacier, Wyoming, USA

One hundred samples were collected from the surface of the Upper Fremont Glacier at equally spaced intervals defined by an 8,100 m 2 snow grid to assess the significance of lateral variability in major-ion concentrations and del oxygen-18 values. For the major ions, the largest concentration range within the snow grid was sodium (0.5056 mg/l) and the smallest concentration range was sulfate (0.125 mg/l). Del oxygen-18 values showed a range of 7.45 per mil. Comparison of the observed variability of each chemical constituent to the variability expected by measurement error indicated substantial lateral variability within the surface-snow layer. Results of the nested ANOVA indicate most of the variance for every constituent is in the values grouped at the two smaller geographic scales (between 506 m 2 and within 506 m 2 sections). Calcium and sodium concentrations and del oxygen-18 values displayed the largest amount of variance at the largest geographic scale (between 2,025 m 2 sections) within the grid and ranged from 14 to 26 per cent of the total variance. The variance data from the snow grid were used to develop equations to evaluate the significance of both positive and negative concentration/value peaks of nitrate and del oxygen-18 with depth, in a 160 m ice core. Solving the equations indicates that both the nitrate and del oxygen-18 ice-core profiles have concentration/value trends that exceed the limits expected from lateral variability. Values of del oxygen-18 in the section from 110-150 m below the surface consistently vary outside the expected limits and possibly represents cooler temperatures during the Little Ice Age from about 1810 to 1725 A.D.

Wyoming↗
USGS1993

Selenium source identification and biogeochemical processes controlling selenium in surface water and biota, Kendrick Reclamation Project, Wyoming, U.S.A.

The major tributaries draining the Kendrick Reclamation Project (KRP) account for an average of 52% of the total Se load measured in the North Platte River downstream from Casper, Wyoming. The Casper Creek drainage basin contributed the largest Se load of the five tributary sites to the North Platte River. The 4-d average Se concentration in water samples from one site in the part of the North Platte River that receives irrigation return flows exceeded the 5 μg/l U.S. Environmental Protection Agency's aquatic life criterion five time during a 50-d monitoring period in 1989. In agreement with the water-quality data, muscle and liver tissue rom rainbow trout collected from the same part of the North Platte River had Se concentrations exceeding levels known to cause reproductive failure and chronic Se poisoning. On the basis of Se: Cl, 18 O/ 16 O and D/H ratios in water from Goose and Rasmus Lee Lakes (closed-basin systems), the large Se concentrations in those lakes were derived by natural evaporation of irrigation water without leaching of soluble forms of Se from soil or rocks. Water samples from Thirtythree Mile Reservoir and Illco Pond (flow-through systems) showed considerable enrichment in Se over evaporative concentration, presumably due to leaching and desorption of Se from soil and rock. The Se: Cl ratios of irrigation drain water collected from the KRP indicate that leaching and desorption of soluble forms of Se from soils and rocks are the dominant processes in drain water. Results of a Wilcoxon matched-pairs test for 43 paired drain-water samples collected during June and August 1988, indicated there is a statistically larger concentration of Se (0.01 significance level) during the June sampling period. The larger concentrations of Se and other chemical constitutents during the early part of the irrigation season probably were due to dissolution of seleniferous salts that have accumulated in soils within the KRP since the last irrigation season. The large Se concentrations in water samples from wetland sites in the KRP were reflected in the aquatic-bird food chain. Most waterfowl and shorebirds nesting at the KRP showed Se concentrations in livers and eggs greater than levels suspected of causing adverse reproductive effects.

Wyoming↗
USGS1990

Geochemistry of batch-extract waters derived from spoil material collected at the Cordero coal mine, Powder River basin, Wyoming

Batch-mixing experiments to evaluate postmining water quality at the Cordero Mine were conducted by the U.S. Geological Survey during 1984 to 1985. Contact of groundwater from the spoil aquifer with fresh spoil material caused only small changes in major-element concentrations and in pH, unless sulfide oxidation or contact with soluble salts, such as epsomite, occurred. In contrast, large changes in major-element concentration resulted when water from the coal aquifer contacted the spoil material. Only three of seven reaction models considered to explain the water quality changes during the batch-mixing experiments were consistent with the thermodynamic and mineralogical data. The three models used to account for the observed water quality changes derived potassium from potassium feldspar; magnesium from chlorite or epsomite or both; sodium from cation exchange and halite; chloride from halite; silica from potassium feldspar and chlorite; sulfate from gypsum, or epsomite or both, and carbon from carbon dioxide. In general, water quality samples obtained from the batch-mixing experiments using water from the coal aquifer had smaller major-ion concentrations than the actual water quality in the spoil aquifer. These differences can be explained by the limited amount of efflorescent salt dissolution and volume of water used in the experiments. Correction ratios calculated for these experiments may be applied to batch-mixing experiments at other mines in the area, to predict postmining water quality. (USGS)

Water-Resources Investigations Report↗
USGS1989

Geochemical processes controlling selenium in ground water after mining, Powder River Basin, Wyoming, U.S.A.

Geochemical data for samples of overburden from three mines in the Powder River Basin indicate a statistically significant (0.01 confidence level) positive correlation ( r = 0.74) between Se and organic C. Results of factor analysis with varimax rotation on the major and trace element data from the rock samples indicate large (>50) varimax loadings for Se in two of the three factors. In Factor 1, the association of Se with constituents common to detrital grains indicates that water transporting the detrital particles into the Powder River Basin also carried dissolved Se. The large (>50) varimax loadings of Se and organic C in Factor 2 probably are due to the organic affinities characteristic of Se. Dissolved Se concentrations in water samples collected at one coal mine are directly related to the dissolved organic C concentrations. Hydrophilic acid concentrations in the water samples from the mine ranged from 35 to 43% of the total dissolved organic C, and hydrophobic acid concentrations ranged from 40 to 49% of the total dissolved organic C. The largest dissolved organic C concentrations in water from the same mine (34–302 mg/l), coupled with the large proportion of acidic components, may saturate adsorption sites on geothite and similar minerals that comprise the aquifer material, thus decreasing the extent of selenite (SeO 3 2− ) adsorption as a sink for Se as the redox state of ground water decreases.

Wyoming↗
USGS1988

Cumulative potential hydrologic impacts of surface coal mining in the eastern Powder River structural basin, northeastern Wyoming

There are 16 existing and six proposed surface coal mines in the eastern Powder River structural basin of northeastern Wyoming. Coal mining companies predict water level declines of 5 ft or more in the Wasatch aquifer to extend form about 1,000 to about 2,000 ft beyond the mine pits. The predicted 5 ft water level decline in the Wyodak coal aquifer generally extends 4-8 mi beyond the lease areas. About 3,000 wells are in the area of potential cumulative water level declines resulting from all anticipated mining. Of these 3,000 wells, about 1,200 are outside the areas of anticipated mining: about 1,000 wells supply water for domestic or livestock uses, and about 200 wells supply water for municipal, industrial, irrigation, and miscellaneous uses. The 1,800 remaining wells are used by coal mining companies. Future surface coal mining probably will result in postmining groundwater of similar quality to that currently present in the study area. By use of geochemical modeling techniques, the results of a hypothetical reaction path exercise indicate the potential for marked improvements in postmining water quality because of chemical reactions as postmining groundwater with a large dissolved solids concentration (3,540 mg/L) moves into a coal aquifer with relatively small dissolved solids concentrations (910 mg/L). Results of the modeling exercise also indicate geochemical conditions that are most ideal for large decreases in dissolved solids concentrations in coal aquifers receiving recharge from a spoil aquifer. (Lantz-PTT)

Water-Resources Investigations Report↗