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J.R. Green

Publications and source records attributed to J.R. Green.

6 recordsLinked to original sources
USGS2016

Isotopic composition of ice cores and meltwater from upper fremont glacier and Galena Creek rock glacier, Wyoming

Meltwater runoff from glaciers can result from various sources, including recent precipitation and melted glacial ice. Determining the origin of the meltwater from glaciers through isotopic analysis can provide information about such things as the character and distribution of ablation on glaciers. A 9.4 m ice core and meltwater were collected in 1995 and 1996 at the glacigenic Galena Creek rock glacier in Wyoming's Absaroka Mountains. Measurements of chlorine‐36 ( 36 Cl), tritium ( 3 H), sulphur‐35 ( 35 S), and delta oxygen‐18 (δ 18 O) were compared to similar measurements from an ice core taken from the Upper Fremont Glacier in the Wind River Range of Wyoming collected in 1991–95. Meltwater samples from three sites on the rock glacier yielded 36 Cl concentrations that ranged from 2.1±1.0×10 6 to 5.8±0.3×10 6 atoms/l. The ice‐core 36 Cl concentrations from Galena Creek ranged from 3.4±0.3×10 5 to 1.0±0.1×10 6 atoms/l. Analysis of an ice core from the Upper Fremont Glacier yielded 36 Cl concentrations of 1.2±0.2×10 6 and 5.2±0.2×10 6 atoms/l for pre‐1940 ice and between 2 ×10 6 and 3×10 6 atoms/l for post‐1980 ice. Purdue's PRIME Lab analyzed the ice from the Upper Fremont Glacier. The highest concentration of 36 Cl in the ice was 77±2×10 6 atoms/l and was deposited during the peak of atmospheric nuclear weapons testing in the late 1950s. This is an order of magnitude greater than the largest measured concentration from both the Upper Fremont Glacier ice core that was not affected by weapons testing fallout and the ice core collected from the Galena Creek rock glacier. Tritium concentrations from the rock glacier ranged from 9.2±0.6 to 13.2±0.8 tritium units (TU) in the meltwater to −1.3±1.3 TU in the ice core. Concentrations of 3 H in the Upper Fremont Glacier ice core ranged from 0 TU in the ice older than 50 years to 6–12 TU in the ice deposited in the last 10 years. The maximum 3H concentration in ice from the Upper Fremont Glacier deposited in the early 1960s during peak weapons testing fallout for this isotope was 360 TU. One meltwater sample from the rock glacier was analyzed for 35 S with a measured concentration of 5.4±1.0 millibecquerel per liter (mBeq/l). Modern precipitation in the Rocky Mountains contains 35 S from 10 to 40 mBeq/L. The δ 18 O results in meltwater from the Galena Creek rock glacier (−17.40±0.1 to −17.98±0.1 per mil) are similar to results for modern precipitation in the Rocky Mountains. Comparison of these isotopic concentrations from the two glaciers suggest that the meltwater at the Galena Creek site is composed mostly of melted snow and rain that percolates through the rock debris that covers the glacier. Additionally, this water from the rock debris is much younger (less than two years) than the reported age of about 2000 years for the subsurface ice at the mid‐glacier coring site. Thus the meltwater from the Galena Creek rock glacier is composed primarily of melted surface snow and rain water rather than melted glacier ice, supporting previous estimates of slow ablation rates beneath the surface debris of the rock glacier.

Geografiska Annaler, Series A: Physical Geography↗
USGS2004

A high resolution record of chlorine-36 nuclear-weapons-tests fallout from Central Asia

The Inilchek Glacier, located in the Tien Shan Mountains, central Asia, is unique among mid-latitude glaciers because of its relatively large average annual accumulation. In July 2000, two ice cores of 162 and 167 meters (m) in length were collected from the Inilchek Glacier for (chlorine-36) 36Cl analysis a part of a collaborative international effort to study the environmental changes archived in mid-latitude glaciers worldwide. The average annual precipitation at the collection site was calculated to be 1.6 m. In contrast, the reported average annual accumulations at the high-latitude Dye-3 glacial site, Greenland, the mid-latitude Guliya Ice Cap, China, and the mid-latitude Upper Fremont Glacier, Wyoming, USA, were 0.52, 0.16 and 0.76 m, respectively. The resolution of the 36Cl record in one of the Inilchek ice cores was from 2 to 10 times higher than the resolution of the records at these other sites and could provide an opportunity for detailed study of environmental changes that have occurred over the past 150 years. Despite the differences in accumulation among these various glacial sites, the 36Cl profile and peak concentrations for the Inilchek ice core were remarkably similar in shape and magnitude to those for ice cores from these other sites. The 36Cl peak concentration from 1958, the year during the mid-1900s nuclear-weapons-tests period when 36Cl fallout was largest, was preserved in the Inilchek core at a depth of 90.56 m below the surface of the glacier (74.14-m-depth water equivalent) at a concentration of 7.7 ?? 105 atoms of 36Cl/gram (g) of ice. Peak 36Cl concentrations from Dye-3, Guliya and the Upper Fremont glacial sites were 7.1 ?? 105, 5.4 ?? 105 and 0.7 ?? 105 atoms of 36Cl/g of ice, respectively. Measurements of 36Cl preserved in ice cores improve estimates of historical worldwide atmospheric deposition of this isotope and allow the sources of 36Cl in ground water to be better identified. ?? 2004 Published by Elsevier B.V.

Conference Paper↗
USGS2000

Use of chlorine-36 to determine regional-scale aquifer dispersivity, eastern Snake River Plain aquifer, Idaho/USA

Chlorine-36 (36Cl) derived from processed nuclear waste that was disposed at the US Department of Energy's Idaho National Engineering and Environmental Laboratory (INEEL) through a deep injection well in 1958, was detected 24-28 yr later in groundwater monitoring wells approximately 26 km downgradient from the source. Groundwater samples covering the period 1966-1995 were selected from the US Geological Survey's archived-sample library at the INEEL and analyzed for 36Cl by accelerator mass spectrometry (AMS). The smaller 36Cl peak concentrations in water from the far-field monitoring wells relative to the input suggest that aquifer dispersivity may be large. However, the sharpness of the 1958 disposal peak of 36Cl is matched by the measured 36Cl concentrations in water from these wells. This implies that a small aquifer dispersivity may be attributed to preferential groundwater flowpaths. Assuming that tracer arrival times at monitoring wells are controlled by preferential flow, a 1-D system-response model was used to estimate dispersivity by comparing the shape of predicted 36Cl-concentration curves to the shape of 36Cl-concentration curves measured in water from these observation wells. The comparisons suggest that a 1-D dispersivity of 5 m provides the best fit to the tracer data. Previous work using a 2-D equivalent porous-media model concluded that longitudinal dispersivity (equivalent to 1-D dispersivity in our model) was 90 m (Ackerman, 1991). A 90 m dispersivity value eliminates the 1958 disposal peak in our model output curves. The implications of the arrival of 36Cl at downgradient monitoring wells are important for three reasons: (1) the arrival times and associated 36Cl concentrations provide quantitative constraints on residence times, velocities, and dispersivities in the aquifer; (2) they help to refine our working hypotheses of groundwater flow in this aquifer and (3) they may suggest a means of estimating the distribution of preferential flowpaths in the aquifer. ?? 2000 Elsevier Science B.V. All rights reserved.

Nuclear Instruments and Methods in Physics Researc↗
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↗