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Correlation between basalt flows and radiochemical and chemical constituents in selected wells in the southwestern part of the Idaho National Laboratory, Idaho

Wastewater discharged to wells and ponds and wastes buried in shallow pits and trenches at facilities at the Idaho National Laboratory (INL) have contributed contaminants to the eastern Snake River Plain (ESRP) aquifer in the southwestern part of the INL. This report describes the correlation between subsurface stratigraphy in the southwestern part of the INL with information on the presence or absence of wastewater constituents to better understand how flow pathways in the aquifer control the movement of wastewater discharged at INL facilities. Paleomagnetic inclination was used to identify subsurface basalt flows based on similar inclination measurements, polarity, and stratigraphic position. Tritium concentrations, along with other chemical information for wells where tritium concentrations were lacking, were used as an indicator of which wells were influenced by wastewater disposal. The basalt lava flows in the upper 150 feet of the ESRP aquifer where wastewater was discharged at the Idaho Nuclear Technology and Engineering Center (INTEC) consisted of the Central Facilities Area (CFA) Buried Vent flow and the AEC Butte flow. At the Advanced Test Reactor (ATR) Complex, where wastewater would presumably pond on the surface of the water table, the CFA Buried Vent flow probably occurs as the primary stratigraphic unit present; however, AEC Butte flow also could be present at some of the locations. At the Radioactive Waste Management Complex (RWMC), where contamination from buried wastes would presumably move down through the unsaturated zone and pond on the surface of the water table, the CFA Buried Vent; Late Basal Brunhes; or Early Basal Brunhes basalt flows are the flow unit at or near the water table in different cores. In the wells closer to where wastewater disposal occurred at INTEC and the ATR-Complex, almost all the wells show wastewater influence in the upper part of the ESRP aquifer and wastewater is present in both the CFA Buried Vent flow and AEC Butte flow. The CFA Buried Vent flow and AEC Butte flow are also present in wells at and north of CFA and are all influenced by wastewater contamination. All wells with the AEC Butte flow present have wastewater influence and 83 percent of the wells with the more prevalent CFA Buried Vent flow have wastewater influence. South and southeast of CFA, most wells are not influenced by wastewater disposal and are completed in the Big Lost Flow and the CFA Buried Vent flow. Wells southwest of CFA are influenced by wastewater disposal and are completed in the Big Lost flow and CFA Buried Vent flow at the top of the aquifer. Basalt stratigraphy indicates that the CFA Buried Vent flow is the predominant flow in the upper part of the ESRP aquifer at and near the RWMC as it is present in all the wells in this area. The Late Basal Brunhes flow, Middle Basal Brunhes flow, Early Basal Brunhes flow, South Late Matuyama flow, and Matuyama flow are also present in various wells influenced by waste disposal. Some wells south of RWMC do not show wastewater influence, and the lack of wastewater influence could be due to low hydraulic conductivities. Several wells south and southeast of CFA also do not show wastewater influence. Low hydraulic conductivities or ESRP subsidence are possible causes for lack of wastewater south of CFA. Multilevel monitoring wells completed much deeper in the aquifer show influence of wastewater in numerous basalt flows. Well Middle 2051 (northwest of RWMC) does not show wastewater influence in its upper three basalt flows (CFA Buried Vent, Late Basal Brunhes, and Middle Basal Brunhes); however, wastewater is present in two deeper flows (the Matuyama and Jaramillo flows). Well USGS 131A (southwest of CFA) and USGS132 (south of RWMC) both show wastewater influence in all the basalt flows sampled in the upper 600 feet of the aquifer. Wells USGS 137A, 105, 108, and 103 completed along the southern boundary of the INL all show wastewater influence in several basalt flows including the G flow, Middle and Early Basal Brunhes flows, the South Late Matuyama flow and the Matuyama flow; however, the strongest wastewater influence appears to be in the South Late Matuyama flow. The concentrations of wastewater constituents in deeper parts of these wells support the concept of groundwater flow deepening in the southwestern part of the INL.

Idaho

Iodine-129 in the Eastern Snake River Plain aquifer at and near the Idaho National Laboratory, Idaho, 2017–18

From 1953 to 1988, approximately 0.941 curies of iodine-129 ( 129 I) were contained in wastewater generated at the Idaho National Laboratory, with almost all of it discharged at or near the Idaho Nuclear Technology and Engineering Center (INTEC). Until 1984, most of the wastewater was discharged directly into the eastern Snake River Plain (ESRP) aquifer through a deep disposal well; however, some wastewater was also discharged into unlined infiltration ponds or leaked from distribution systems below the INTEC. During 2017–18, the U.S. Geological Survey, in cooperation with the U.S. Department of Energy, collected samples for 129 I from 30 wells that monitor the ESRP aquifer to track concentrations and changes of the carcinogenic radionuclide that has a 15.7 million-year half-life. Concentrations of 129 I in the aquifer ranged from 0.000016 ± 0.000001 to 0.88+/- 0.03 picocuries per liter (pCi/L), and concentrations generally decreased in wells near the INTEC as compared with previously collected samples. The average concentration of 15 wells sampled during 5 different sample periods decreased from 1.15 pCi/L in 1990–91 to 0.168 pCi/L in 2017–18, but average concentrations were similar to 2011–12 within analytical uncertainty. All but four wells within a 3-mile radius of the INTEC showed decreases in concentration, and all samples had concentrations less than the U.S. Environmental Protection Agency’s maximum contaminant level of 1 pCi/L. These decreases are attributed to the discontinuation of disposal of 129 I in wastewater and to dilution and dispersion in the aquifer. Some wells southeast of INTEC showed increasing trends; these increases were attributed to variable transmissivity. Although wells near INTEC sampled in 2017–18 showed decreases in concentrations compared with data collected previously, some wells south of the INL boundary showed small increases. These increases are attributed to historical variable discharge rates of wastewater that eventually moved to these well locations as a pulse of water from a particular disposal period.

Idaho

An update of hydrologic conditions and distribution of selected constituents in water, Eastern Snake River Plain aquifer and perched groundwater zones, Idaho National Laboratory, Idaho, emphasis 2016–18

Since 1952, wastewater discharged to infiltration ponds (also called percolation ponds) and disposal wells at the Idaho National Laboratory (INL) has affected water quality in the eastern Snake River Plain (ESRP) aquifer and perched groundwater zones underlying the INL. The U.S. Geological Survey (USGS), in cooperation with the U.S. Department of Energy, maintains groundwater-monitoring networks at the INL to determine hydrologic trends and to delineate the movement of radiochemical and chemical wastes in the aquifer and in perched groundwater zones. This report presents an analysis of water-level and water-quality data collected from the ESRP aquifer and perched groundwater wells in the USGS groundwater monitoring networks during 2016–18. From March–May 2015 to March–May 2018, water levels in wells completed in the ESRP aquifer declined in the northern part of the INL and increased in the southwestern part. Water-level decreases ranged from 0.5 to 3.0 feet (ft) in the northern part of the INL and increases ranged from 0.5 to 3.0 ft in the southwestern part. Detectable concentrations of radiochemical constituents in water samples from wells in the ESRP aquifer at the INL generally decreased or remained constant during 2016–18. Decreases in concentrations were attributed to radioactive decay, changes in waste-disposal methods, and dilution from recharge and underflow. In 2018, concentrations of tritium in water samples collected from 46 of 111 aquifer wells were greater than the reporting level of three times the sample standard deviation and ranged from 260±50 to 5,100±190 picocuries per liter (pCi/L). Tritium concentrations in water from 10 wells completed in deep perched groundwater above the ESRP aquifer near the Advanced Test Reactor (ATR) Complex generally were greater than or equal to the reporting level during at least one sampling event during 2016–18, and concentrations ranged from 150 ±50 to 12,900 ±200 pCi/L. Concentrations of strontium-90 in water from 17 of 60 ESRP aquifer wells sampled during April or October 2018 exceeded the reporting level, ranging from 2.2±0.7 to 363±19 pCi/L. Strontium-90 was not detected in the ESRP aquifer beneath the ATR Complex. During at least one sampling event during 2016–18, concentrations of strontium-90 in water from eight wells completed in deep perched groundwater above the ESRP aquifer at the ATR Complex equaled or exceeded the reporting levels, and concentrations ranged from 0.57±0.17 to 34.3±1.2 pCi/L. During 2016–18, concentrations of cesium-137 were less than the reporting level in all but one ESRP aquifer well, and concentrations of plutonium-238, -239, and -240 (undivided), and americium-241 were less than the reporting level in water samples from all ESRP aquifer wells. In April 2009, the dissolved chromium concentration in water from one ESRP aquifer well, USGS 65, south of the ATR Complex equaled the maximum contaminant level (MCL) of 100 micrograms per liter (μg/L). In April 2018, the concentration of chromium in water from that well had decreased to 76.0 μg/L, less than the MCL. Concentrations in water samples from 62 other ESRP aquifer wells sampled ranged from less than 0.6 to 21.6 μg/L. During 2016–18, dissolved chromium was detected in water from all wells completed in deep perched groundwater above the ESRP aquifer at the ATR Complex, and concentrations ranged from 4.2 to 98.8 μg/L. In 2018, concentrations of sodium in water from most ESRP aquifer wells in the southern part of the INL were greater than the western tributary background concentration of 8.3 milligrams per liter (mg/L). After the new percolation ponds were put into service in 2002 southwest of the Idaho Nuclear Technology and Engineering Center (INTEC), concentrations of sodium in water samples from the Rifle Range well increased steadily until 2008, when concentrations generally began decreasing. The increases and decreases were attributed to disposal variability in the new percolation ponds. During 2016–18, dissolved sodium concentrations in water from 18 wells completed in deep perched groundwater above the ESRP aquifer at the ATR Complex ranged from 6.37 to 143 mg/L. In 2018, concentrations of chloride in most water samples from ESRP aquifer wells south of the INTEC and at the Central Facilities Area exceeded the background concentrations. Chloride concentrations in water from wells south of the INTEC generally have decreased since 2002 when chloride disposal to the old percolation ponds was discontinued. After the new percolation ponds southwest of the INTEC were put into service in 2002, concentrations of chloride in water samples from one well rose steadily until 2008 then began decreasing. During 2016–18, dissolved chloride concentrations in deep perched groundwater above the ESRP aquifer from 18 wells at the ATR Complex ranged from 3.89 to 176 mg/L. In 2018, sulfate concentrations in water samples from ESRP aquifer wells in the south-central part of the INL exceeded the background concentration of sulfate and ranged from 22 to 151 mg/L. The greater-than-background concentrations in water from these wells probably resulted from sulfate disposal at the ATR Complex infiltration ponds or the old INTEC percolation ponds. In 2018, sulfate concentrations in water samples from wells near the Radioactive Waste Management Complex (RWMC) mostly were greater than background concentrations and could have resulted from well construction techniques and (or) waste disposal at the RWMC or the ATR complex. The maximum dissolved sulfate concentration in shallow perched groundwater above the ESRP aquifer near the ATR Complex was 215 mg/L in well CWP 3 in April 2016. During 2018, dissolved sulfate concentrations in water from wells completed in deep perched groundwater above the ESRP aquifer near the cold-waste ponds at the ATR Complex ranged from 65.8 to 171 mg/L. In 2018, concentrations of nitrate in water from most ESRP aquifer wells at and near the INTEC exceeded the western tributary background concentration of 0.655 mg/L. Concentrations of nitrate in wells southwest of the INTEC and farther away from the influence of disposal areas and the Big Lost River show a general decrease in nitrate concentration through time. Two wells south of the INTEC show increasing trends that could be the result of wastewater beneath the INTEC tank farm being mobilized to the aquifer. During 2016–18, water samples from several ESRP aquifer wells were collected and analyzed for volatile organic compounds (VOCs). Sixteen VOCs were detected. At least 1 and as many as 7 VOCs were detected in water samples from 15 wells. The primary VOCs detected include carbon tetrachloride, trichloromethane, tetrachloroethene, 1,1,1-trichloroethane, and trichloroethene. In 2016–18, concentrations for all VOCs were less than their respective MCLs for drinking water, except carbon tetrachloride in water from two wells and trichloroethene in one well. During 2016–18, variability and bias were evaluated from 37 replicate and 15 blank quality-assurance samples. Results from replicate analyses were investigated to evaluate sample variability. Constituents with acceptable reproducibility were major ions, trace elements, nutrients, and VOCs. All radiochemical constituents had acceptable reproducibility except for gross alpha- and beta-particle radioactivity. The gross alpha- and beta-particle radioactivity samples that did not meet reproducibility criteria had low concentrations. Bias from sample contamination was evaluated from equipment, field, and source-solution blanks. Cadmium had a concentration slightly greater than its reporting level in a source-solution blank, and chloride and ammonia had concentrations that were slightly greater than their respective reporting levels in field and equipment blanks. Subtracting concentrations of chloride and ammonia in field blanks from the concurrently collected equipment blank indicates that adjusted concentrations for chloride and ammonia in the equipment blanks were less than their respective reporting levels. Therefore, no sample bias was observed for any of the sample periods.

Idaho

An update of hydrologic conditions and distribution of selected constituents in water, eastern Snake River aquifer and perched groundwater zones, Idaho National Laboratory, Idaho, emphasis 2019–21

Since 1952, wastewater discharged to infiltration ponds (also called “percolation ponds”) and disposal wells at the Idaho National Laboratory (INL) has affected water quality in the eastern Snake River Plain (ESRP) aquifer and perched groundwater zones underlying the INL. The U.S. Geological Survey (USGS), in cooperation with the U.S. Department of Energy (DOE), maintains groundwater-monitoring networks at the INL to determine hydrologic trends and to delineate the movement of radiochemical and chemical wastes in both the aquifer and perched groundwater zones. This report presents an analysis of water-level and water-quality data collected from the ESRP aquifer and perched groundwater wells from the USGS groundwater monitoring networks during 2019–21. From March–May 2018 to March–May 2021, water levels in wells completed in the ESRP aquifer increased in the northern part of the INL and decreased in the southwestern part. Water-level increases ranged from 0.02 to 1.04 feet in the northern part and decreases ranged from 0.03 to 2.94 feet in the southwestern part of the INL. Detectable concentrations of radiochemical constituents in water samples from wells in the ESRP aquifer at the INL generally decreased or remained constant during 2019–21. Decreases in concentrations were attributed to radioactive decay, changes in waste-disposal methods, and dilution from recharge and underflow. In 2021, tritium was detected above reporting levels in water samples collected from 46 of 105 aquifer wells and ranged from 150±50 to 4,280±150 picocuries per liter (pCi/L). Tritium concentrations from eight wells completed in deep perched groundwater near the Advanced Test Reactor Complex (ATRC) generally were greater than or equal to the reporting level during at least one sampling event during 2019–21, and concentrations ranged from 160±50 to 2,097±107 pCi/L. Concentrations of strontium-90 in water from 12 of 45 aquifer wells sampled in 2021 exceeded the reporting level, and concentrations ranged from 2.5±0.7 to 299±6 pCi/L. During 2021, concentrations of strontium-90 from five wells completed in deep perched groundwater at the ATRC equaled or exceeded the reporting levels, and concentrations ranged from 3±0.9 pCi/L to 27.8±1.3 pCi/L. Concentrations of cesium-137 were less than the reporting level in all but one aquifer well, and concentrations of plutonium-238, plutonium-239, -240 (undivided), and americium-241 were less than the reporting level in water samples from all aquifer wells sampled during this study period. Dissolved chromium concentrations in water samples from 64 ESRP aquifer wells ranged from less than (<) 0.5 to 76.4 micrograms per liter (μg/L). During 2019–21, dissolved chromium was detected in water from wells completed in deep perched groundwater above the ESRP aquifer at the ATRC, and concentrations ranged from <1 to 82.1 μg/L. In 2021, concentrations of dissolved sodium in water from most ESRP aquifer wells in the southern part of the INL were greater than the western tributary groundwater background concentration of 8.3 milligrams per liter (mg/L). During 2021, dissolved sodium concentrations in water from 15 wells completed in deep perched groundwater ranged from 11.7 to 122.5 mg/L. Variations in sodium concentrations in aquifer wells and perched groundwater zones are attributed to either migration of remnant water from the former chemical-waste ponds or disposal volume and composition variability in percolation ponds installed in 2008. In 2021, concentrations of chloride in most water samples from ESRP aquifer wells south of the Idaho Nuclear Technology and Engineering Center (INTEC) and at the Central Facilities Area (CFA) exceeded background concentrations. Chloride concentrations in water from wells south of the INTEC have generally decreased because of discontinued chloride disposal to the legacy percolation ponds since 2002 when the discharge of wastewater was discontinued. During 2019–21, dissolved chloride concentrations in deep perched groundwater above the ESRP aquifer from 18 wells at the ATRC ranged from 8.15 to 231 mg/L. In 2021, sulfate concentrations in water samples from ESRP aquifer wells in the south-central part of the INL that exceeded the background concentration of sulfate, ranged from 21 to 141 mg/L. The greater-than-background concentrations in water from these wells are attributed to sulfate disposal at the ATRC infiltration ponds or the legacy INTEC percolation ponds. In 2021, sulfate concentrations in water samples from aquifer wells near the Radioactive Waste Management Complex (RWMC) were mostly greater than background concentrations. The maximum dissolved sulfate concentration in shallow perched groundwater near the ATRC was 575 mg/L in 2021. During 2021, dissolved sulfate concentrations in water from wells completed in deep perched groundwater near the cold waste ponds at the ATRC ranged from 22.3 to 519 mg/L. In 2021, concentrations of nitrate in water from most ESRP aquifer wells at and near the INTEC exceeded the western tributary groundwater background concentration of 0.655 mg/L. Concentrations of nitrate in aquifer wells southwest of INTEC and farther away from the influence of disposal areas and the Big Lost River, in intermittent source of surface water recharge to the aquifer, show a general decrease in nitrate concentration over time. Two aquifer wells south of INTEC show increasing trends that could result from wastewater beneath the INTEC tank farm being mobilized to the aquifer. During 2019–21, water samples from several ESRP aquifer wells were collected and analyzed for volatile organic compounds (VOCs). Twelve VOCs were detected, and 1–4 VOCs were detected in water samples from 10 wells. The most frequently detected VOCs include carbon tetrachloride (tetrachloromethane), trichloromethane, tetrachloroethene, 1,1,1-trichloroethane, and trichloroethene. In 2019–21, concentrations for all VOCs were less than their respective maximum contaminant levels (MCLs) for drinking water, except carbon tetrachloride in one well, trichloroethene in two wells, and vinyl chloride in one well. During 2019–21, variability and bias were evaluated from 34 replicate and 14 blank quality-assurance samples. Results from replicate analyses were investigated to evaluate sample variability. Constituents with acceptable reproducibility were major ions, trace elements, nutrients, and VOCs. All radiochemical constituents including gross alpha- and beta- radioactivity, strontium-90, cesium-137, and tritium, had acceptable reproducibility. Bias from sample contamination was evaluated from equipment, field, and source-solution blanks. Chloride and sulfate were detected slightly above their respective method detection limits in equipment and field blanks, but at concentrations well below the co-collected sample for that well. These chloride and sulfate detections in the field and equipment blanks were inconsequential because they weren’t detected above the analysis-specific variability for those constituents as determined by replicate sample result evaluation. None of the detections of nutrients and trace inorganic constituents were high enough to indicate environmental sample or analytical procedure bias.

Idaho

Natural thorium resources and recovery: Options and impacts

This paper reviews the front end of the thorium fuel cycle, including the extent and variety of thorium deposits, the potential sources of thorium production, and the physical and chemical technologies required to isolate and purify thorium. Thorium is frequently found within rare earth element&ndash;bearing minerals that exist in diverse types of mineral deposits, often in conjunction with other minerals mined for their commercial value. It may be possible to recover substantial quantities of thorium as a by-product from active titanium, uranium, tin, iron, and rare earth mines. Incremental physical and chemical processing is required to obtain a purified thorium product from thorium minerals, but documented experience with these processes is extensive, and incorporating thorium recovery should not be overly challenging. The anticipated environmental impacts of by-product thorium recovery are small relative to those of uranium recovery since existing mining infrastructure utilization avoids the opening and operation of new mines and thorium recovery removes radionuclides from the mining tailings.

Nuclear Technology

Geohydrologic considerations in the management of radioactive waste

Nongaseous radioactive wastes occur as liquids containing high-level concentrations of radionuclides, liquids containing low concentrations of radionuclides, and solids contaminated by radioactivity. Whether released by accident or design into the earth or onto the earth’s surface, only water is capable of transporting significant quantities of radionuclides away from burial sites. Geohydrologic information that must be determined to predict the velocity and direction of waste movement from a site include climate, hydrology, detailed subsurface geology, permeability, porosity, sorptive potential, seismic potential, and geologic history of the area. Since the late 1960’s mathematical models have been used to make predictions of waste transport in some hydrologic systems. Intensive field investigations at each site are needed before these models can be used.

Nuclear Technology

The effect of composition of selected groundwaters from the Basin and Range Province on plutonium, neptunium, and Americium speciation

The speciation of plutonium, neptunium, and americium was determined in groundwaters from four sources in the Basin and Range Province: the lower carbonate aquifer, Nevada Test Site (NTS) (Crystal Pool); alluvial fill, Frenchman Flat, NTS (well 5C); Hualapai Valley, Arizona (Red Lake south well); and Tularosa Basin, New Mexico (Rentfrow well). The results were interpreted to indicate that plutonium and, to a lesser extent, neptunium are least soluble in reducing groundwaters containing a large concentration of sulfate ion and a small concentration of strongly complexing anions. The results further emphasize the desirability of including studies such as this among the other site-selection criteria for nuclear waste repositories.

Arizoan, Nevada, New Mexico

Plutonium, americium, and neptunium speciation in selected groundwaters

As part of a continuing study, plutonium, americium, and neptunium speciation was determined at 25 and 90°C in four groundwaters from diverse sources: the Sparta aquifer in Louisiana, near the Vacherie salt dome; Mansfield No. 2 well in the Palo Duro Basin, Texas; the Stripa mine in Sweden; and the Waste Isolation Pilot Plant (WIPP) in New Mexico. Plutonium generally was soluble in Sparta and Stripa waters, regardless of temperature or initial oxidation state. Solubility in Mansfield water was high, except in 90 °C experiments using low-oxidation-state plutonium. The WIPP water had the least ability to maintain plutonium in solution; solubility after 30 days exceeded 50% only in experiments at 25 °C using Pu(V) and Pu(VI). Neptunium generally was soluble in all waters and was present exclusively as Np(V) and Np(VI), regardless of initial oxidation state. The solubility of americium was consistently high in Sparta groundwater at both temperatures and in Mansfield and WIPP waters at 25°C, but was < 50% after 30 days in Stripa water at both temperatures and in Mansfield and WIPP waters at 90°C. The results indicated that plutonium and neptunium solubilities were determined by the oxidation-reduction properties of the waters, i.e., their abilities to convert these elements to soluble oxidation states. This was not the case for americium, however; Am(IV) was not detected, and the solubility of this element was determined entirely by the chemical properties of Am(III).

Nuclear Technology

Leaching of plutonium from a radioactive waste glass by eight groundwaters from the western United States

The leachability of a radioactive waste glass formulated to Battelle Pacific Northwest Laboratory specification 80-270 has been studied using eight actual groundwaters with a range of chemical compositions as leachants. Waters collected from the Grande Ronde Basalt (Washington State) and from alluvial deposits in the Hualapai Valley (Arizona) were the most effective at removing plutonium from this glass. Leaching was shown to be incongruent; plutonium was removed from the glass more slowly than the overall glass matrix. The results of these experiments indicate the need to study the leachability of actual waste forms using the actual projected groundwaters that are most likely to come into contact with the waste should a radioactive waste repository be breached.

western United States

An update of hydrologic conditions and distribution of selected constituents in water, eastern Snake River Plain aquifer and perched groundwater zones, Idaho National Laboratory, Idaho, emphasis 2009–11

Since 1952, wastewater discharged to infiltration ponds (also called percolation ponds) and disposal wells at the Idaho National Laboratory (INL) has affected water quality in the eastern Snake River Plain (ESRP) aquifer and perched groundwater zones underlying the INL. The U.S. Geological Survey (USGS), in cooperation with the U.S. Department of Energy, maintains groundwater monitoring networks at the INL to determine hydrologic trends, and to delineate the movement of radiochemical and chemical wastes in the aquifer and in perched groundwater zones. This report presents an analysis of water-level and water-quality data collected from aquifer, multilevel monitoring system (MLMS), and perched groundwater wells in the USGS groundwater monitoring networks during 2009–11. Water in the ESRP aquifer primarily moves through fractures and interflow zones in basalt, generally flows southwestward, and eventually discharges at springs along the Snake River. The aquifer primarily is recharged from infiltration of irrigation water, infiltration of streamflow, groundwater inflow from adjoining mountain drainage basins, and infiltration of precipitation. From March–May 2009 to March–May 2011, water levels in wells generally declined in the northern part of the INL. Water levels generally rose in the central and eastern parts of the INL. Detectable concentrations of radiochemical constituents in water samples from aquifer wells or MLMS equipped wells in the ESRP aquifer at the INL generally decreased or remained constant during 2009–11. Decreases in concentrations were attributed to radioactive decay, changes in waste-disposal methods, and dilution from recharge and underflow. In 2011, concentrations of tritium in groundwater from 50 of 127 aquifer wells were greater than or equal to the reporting level and ranged from 200±60 to 7,000±260 picocuries per liter. Tritium concentrations from one or more discrete zones from four wells equipped with MLMS were greater than or equal to reporting levels in water samples collected at various depths. Tritium concentrations in water from wells completed in shallow perched groundwater at the Advanced Test Reactor Complex (ATR Complex) were less than the reporting levels. Tritium concentrations in deep perched groundwater at the ATR Complex equaled or exceeded the reporting level in 12 wells during at least one sampling event during 2009–11 at the ATR Complex. Concentrations of strontium-90 in water from 20 of 76 aquifer wells sampled during April or October 2011 exceeded the reporting level. Strontium-90 was not detected within the ESRP aquifer beneath the ATR Complex. During at least one sampling event during 2009–11, concentrations of strontium-90 in water from 10 wells completed in deep perched groundwater at the ATR Complex equaled or exceeded the reporting levels. During 2009–11, concentrations of plutonium-238, and plutonium-239, -240 (undivided), and americium-241 were less than the reporting level in water samples from all aquifer wells and in all wells equipped with MLMS. Concentrations of cesium-137 were equal to or slightly above the reporting level in 8 aquifer wells and from 2 wells equipped with MLMS. The concentration of chromium in water from one well south of the ATR Complex was 97 micrograms per liter (μg/L) in April 2011, just less than the maximum contaminant level (MCL) of 100 μg/L. Concentrations of chromium in water samples from 69 other wells sampled ranged from 0.8 μg/L to 25 μg/L. During 2009–11, dissolved chromium was detected in water from 15 wells completed in perched groundwater at the ATR Complex. In 2011, concentrations of sodium in water from most wells in the southern part of the INL were greater than the background concentration of 10 milligrams per liter (mg/L); the highest concentrations were at or near the Idaho Nuclear Engineering and Technology Center (INTEC). After the newpercolation ponds were put into service in 2002 southwest of the INTEC, concentrations of sodium in water samples from the Rifle Range well rose steadily until 2008, when the concentrations generally began decreasing. The increases and decreases were attributed to disposal variability in the new percolation ponds. Concentrations of sodium in most wells equipped with MLMS generally were consistent with depth. During 2011, dissolved sodium concentrations in water from 17 wells completed in deep perched groundwater at the ATR Complex ranged from 6 to 146 mg/L. In 2011, concentrations of chloride in most water samples from aquifer wells south of the INTEC and at the Central Facilities Area exceeded the background concentrations of 15 mg/L, but were less than the secondary MCL of 250 mg/L. Chloride concentrations in water from wells south of the INTEC have generally increased because of increased chloride disposal to the old percolation ponds since 1984 when discharge of wastewater to the INTEC disposal well was discontinued. After the new percolation ponds were put into service in 2002 southwest of the INTEC, concentrations of chloride in water samples from one well rose steadily until 2008 then began decreasing. Chloride concentrations in water from all but one well completed in the ESRP aquifer at or near the ATR Complex were less than background and ranged between 10 and 14 mg/L during 2011, similar to concentrations detected during the 2006–08 reporting period. During 2011, chloride concentrations in water from two aquifer wells at the Radioactive Waste Management Complex (RWMC) were slightly greater than concentrations detected during the 2006–08 reporting period. The vertical distribution of chloride concentrations in wells equipped with MLMS were generally consistent within zones during 2009–11 and ranged from about 8 to 20 mg/L. During April 2011, dissolved chloride concentrations in shallow perched groundwater at the ATR Complex ranged from 7 to 13 mg/L in water from three wells. Dissolved chloride concentrations in deep perched groundwater at the ATR Complex during 2011 ranged from 4 to 54 mg/L. In 2011, sulfate concentrations in water samples from 11 aquifer wells in the south-central part of the INL equaled or exceeded the background concentration of sulfate and ranged from 40 to 167 mg/L. The greater-than-background concentrations in water from these wells probably resulted from sulfate disposal at the ATR Complex infiltration ponds or the old INTEC percolation ponds. In 2011, sulfate concentrations in water samples from two wells near the RWMC were greater than background levels and could have resulted from well construction techniques and (or) waste disposal at the RWMC. The vertical distribution of sulfate concentrations in three wells near the southern boundary of the INL was generally consistent with depth, and ranged between 19 and 25 mg/L. The maximum dissolved sulfate concentration in shallow perched groundwater near the ATR Complex was 400 mg/L in well CWP 1 in April 2011. During 2009–11, the maximum concentration of dissolved sulfate in deep perched groundwater at the ATR Complex was 1,550 mg/L in a well located west of the chemical-waste pond. In 2011, concentrations of nitrate in water from most wells at and near the INTEC exceeded the regional background concentrations of 1 mg/L and ranged from 1.6 to 5.95 mg/L. Concentrations of nitrate in wells south of INTEC and farther away from the influence of disposal areas and the Big Lost River show a general decrease in nitrate concentrations through time. During 2009–11, water samples from 30 wells were collected and analyzed for volatile organic compounds (VOCs). Six VOCs were detected. At least one and up to five VOCs were detected in water samples from 10 wells. The primary VOCs detected include carbon tetrachloride, chloroform, tetrachloroethylene, 1,1,1-trichloroethane, and trichloroethylene. In 2011, concentrations for all VOCs were less than their respective MCL for drinking water, except carbon tetrachloride in water from two wells. During 2009–11, variability and bias were evaluated from 56 replicate and 16 blank quality-assurance samples. Results from replicate analyses were investigated to evaluate sample variability. Constituents with acceptable reproducibility were stable isotope ratios, major ions, nutrients, and VOCs. All radiochemical constituents and trace metals had acceptable reproducibility except for gross beta-particle radioactivity, aluminum, antimony, and cobalt. Bias from sample contamination was evaluated from equipment, field, container, and source-solution blanks. No detectable constituent concentrations were reported for equipment blanks of the thief samplers and sampling pipes or for the source-solution and field blanks. Equipment blanks of bailers had detectable concentrations of strontium-90, sodium, chloride, and sulfate, and the container blank had a detectable concentration of dichloromethane.

Idaho

Ongoing research experiments at the former Soviet nuclear test site in eastern Kazakhstan

Degelen mountain, located in Eastern Kazakhstan near the city of Semipalatinsk, was once the Soviets most active underground nuclear test site . Two hundred fifteen nuclear tests were conducted in 181 tunnels driven horizontally into its many ridges--almost twice the number of tests as at any other Soviet underground nuclear test site . It was also the site of the first Soviet underground nuclear test --a 1-kiloton device detonated on October 11, 1961. Until recently, the details of testing at Degelen were kept secret and have been the subject of considerable speculation. However, in 1991, the Semipalatinsk test site became part of the newly independent Republic of Kazakhstan ; and in 1995, the Kazakhstani government concluded an agreement with the U.S. Department of Defense to eliminate the nuclear testing infrastructure in Kazakhstan . This agreement, which calls for the "demilitarization of the infrastructure directly associated with the nuclear weapons test tunnels," has been implemented as the "Degelen Mountain Tunnel Closure Program." The U.S. Defense Threat Reduction Agency, in partnership with the Department of Energy, has permitted the use of the tunnel closure project at the former nuclear test site as a foundation on which to support cost-effective, research-and-development-funded experiments. These experiments are principally designed to improve U.S. capabilities to monitor and verify the Comprehensive Test Ban Treaty (CTBT), but have provided a new source of information on the effects of nuclear and chemical explosions on hard, fractured rock environments. These new data extends and confirms the results of recent Russian publications on the rock environment at the site and the mechanical effects of large-scale chemical and nuclear testing. In 1998, a large-scale tunnel closure experiment, Omega-1, was conducted in Tunnel 214 at Degelen mountain. In this experiment, a 100-ton chemical explosive blast was used to test technologies for monitoring the Comprehensive Nuclear Test Ban Treaty, and to calibrate a portion of the CTBT's International Monitoring System. This experiment has also provided important benchmark data on the mechanical behavior of hard, dense, fractured rock, and has demonstrated the feasibility of fielding large-scale calibration explosions, which are specified as a "confidence-building measure" in the CTBT Protocol. Two other large-scale explosion experiments, Omega-2 and Omega-3, are planned for the summer of 1999 and 2000. Like the Tunnel 214 test, the 1999 experiment will include close-in monitoring of near-source effects, as well as contributing to the calibration of key seismic stations for the Comprehensive Test Ban Treaty. The Omega-3 test will examine the effect of multiple blasts on the fractured rock environment.

Conference Paper

Vulnerabilities and opportunities at the nexus of electricity, water and climate

The articles in this special issue examine the critical nexus of electricity, water, and climate, emphasizing connections among resources; the prospect of increasing vulnerabilities of water resources and electricity generation in a changing climate; and the opportunities for research to inform integrated energy and water policy and management measures aimed at reducing vulnerability and increasing resilience. Here, we characterize several major themes emerging from this research and highlight some of the uptake of this work in both scientific and public spheres. Underpinning much of this research is the recognition that water resources are expected to undergo substantial changes based on the global warming that results primarily from fossil energy-based carbon emissions. At the same time, the production of electricity from fossil fuels, nuclear power, and some renewable technologies (biomass, geothermal and concentrating solar power) can be highly water-intensive. Energy choices now and in the near future will have a major impact not just on the global climate, but also on water supplies and the resilience of energy systems that currently depend heavily on them.

Environmental Research Letters

Experimental approaches to assessing the impact of a cesium chloride radiological dispersal device

The US EPA, as a part of the Chemical, Biological, Radiological-Nuclear, and Explosives (CBRNE) Research and Technology Initiative (CRTI) project team, is currently working to assess the impacts of an urban radiological dispersion device (RDD) and to develop containment and decontamination strategies. Three efforts in this area are currently underway: development of a laboratory-scale cesium chloride deposition method to mimic a RDD; assessment of cesium (Cs) penetration depth and pathways in urban materials using two dimensional (2-D) mapping laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS); and experimental determination of distribution coefficients (kd) for Cs in water-building material systems. It is critical that, when performing laboratory-scale experiments to assess the fate of Cs from an RDD, the Cs particle deposition method mimics the RDD deposition. Once Cs particles are deposited onto urban surfaces, 2-D mapping of Cs concentrations using LA-ICP-MS is a critical tool for determining Cs transport pathways through these materials. Lastly, distribution coefficients are critical for understanding the transport of Cs in urban settings when direct measurements of its penetration depth are unavailable. An assessment of the newly developed deposition method along with preliminary results from the penetration experiments are presented in this paper.

Conference Paper

Nuclear magnetic resonance logging of a deep test well for estimation of aquifer and confining-unit hydraulic properties, Long Island, New York

A 1,200-foot deep well in southwestern Nassau County, Long Island, N.Y. was selected to evaluate the application of a nuclear magnetic resonance (NMR) logging tool. Technological advances in NMR borehole systems have allowed for reduced probe length and diameter, and focused measurement at specific diameters beyond the disturbed zone surrounding a well. This 3-inch-diameter NMR tool was specifically developed for use in deep 4-inch-diameter polyvinyl chloride cased wells common to Long Island. Selected intervals of the Magothy and Lloyd aquifers and the Raritan confining unit were logged for the evaluation. Unlike other petrophysical logs that respond to the rock matrix and fluid properties and are strongly dependent on mineralogy, NMR logs respond to the presence of hydrogen protons in the formation fluid to determine water fraction and pore-size distribution. NMR log analysis provided estimates of the clay-bound, capillary-bound, and mobile water fraction and hydraulic conductivity of aquifers and confining units penetrated by the well. NMR-estimated porosity and mobile water fraction for the Magothy aquifer (0.34 and 0.22 respectively), Magothy/Raritan(?) (0.35 and 0.30), Raritan confining unit (0.30 and 0.13), Raritan clay and silt (0.23 and 0.01), and the Lloyd aquifer (0.27 and 0.19) was determined from the NMR log. Hydraulic conductivity was estimated from the NMR-log data using the Schlumberger- Doll Research and sum of squared echoes equations with empirically derived constants for unconsolidated aquifers. Average hydraulic conductivity of the Magothy aquifer was 70 ft/d, the Raritan confining unit was 9.0 ft/d overall, the clay-rich lower part 0.24 ft/d, and the Lloyd aquifer was 56 ft/d. The coarse sandy Magothy/Raritan(?) unit between the Magothy aquifer and the top of the Raritan confining unit had the highest hydraulic conductivity of 345 ft/d. The hydraulic-conductivity estimates from the NMR log analysis for the Magothy and Lloyd aquifers were consistent with published values and that estimated for the Lloyd aquifer from a specific-capacity test at the well site.

New York

Atomic weights of the elements. Review 2000 (IUPAC Technical Report)

A consistent set of internationally accepted atomic weights has long been an essential aim of the scientific community because of the relevance of these values to science and technology, as well as to trade and commerce subject to ethical, legal, and international standards. The standard atomic weights of the elements are regularly evaluated, recommended, and published in updated tables by the Commission on Atomic Weights and Isotopic Abundances (CAWIA) of the International Union of Pure and Applied Chemistry (IUPAC). These values are invariably associated with carefully evaluated uncertainties. Atomic weights were originally determined by mass ratio measurements coupled with an understanding of chemical stoichiometry, but are now based almost exclusively on knowledge of the isotopic composition (derived from isotope-abundance ratio measurements) and the atomic masses of the isotopes of the elements. Atomic weights and atomic masses are now scaled to a numerical value of exactly 12 for the mass of the carbon isotope of mass number 12. Technological advances in mass spectrometry and nuclear-reaction energies have enabled atomic masses to be determined with a relative uncertainty of better than 1 ×10−7 . Isotope abundances for an increasing number of elements can be measured to better than 1 ×10−3 . The excellent precision of such measurements led to the discovery that many elements, in different specimens, display significant variations in their isotope-abundance ratios, caused by a variety of natural and industrial physicochemical processes. While such variations increasingly place a constraint on the uncertainties with which some standard atomic weights can be stated, they provide numerous opportunities for investigating a range of important phenomena in physical, chemical, cosmological, biological, and industrial processes. This review reflects the current and increasing interest of science in the measured differences between source-specific and even sample-specific atomic weights. These relative comparisons can often be made with a smaller uncertainty than is achieved in the best calibrated “absolute ” (=SI-traceable) atomic-weight determinations. Accurate determinations of the atomic weights of certain elements also influence the values of fundamental constants such as the Avogadro, Faraday, and universal gas constants. This review is in two parts: the first summarizes the development of the science of atomic-weight determinations during the 20th century; the second summarizes the changes and variations that have been recognized in the values and uncertainties of atomic weights, on an element-by-element basis, in the latter part of the 20th century.

Pure and Applied Chemistry

Seismic environment of the Burro Flats site, Ventura County, California: a brief, limited literature review

A limited review of available literature suggests that the maximum horizontal ground acceleration at the Burro Flats site from earthquakes in the region could range from less than 0.1 to 0.49 g. A magnitude 8 earthquake on the nearby San Andreas fault could produce ground acceleration in the range 0.18 to 0.31 g, and an expectable larger earthquake on that fault could produce larger accelerations. Ground motion from possible smaller but closer earthquakes ranges up to 0.49 g for an earthquake of magnitude 6.5 on the adjacent "Burro Flats fault". Estimation of these accelerations is dependent on determining the geologic environment of the site, the appropriate earthquake magnitudes to be assigned significant faults in that environment, and the attenuation of shaking between the earthquake epicenters and the site. The site lies within a tectonically active region--the historically active San Andreas fault is only 34 miles to the northeast, and lesser faults showing evidence of late Quaternary displacement are located closer to the site. Evidence for youthfulness of these lesser faults varies, and except for the active Newport-Inglewood zone and the Santa Ynez fault, they qualify as possible but as yet-unproven active faults. All known faults with appropriate length to site-distance ratios that are reasonably classed as late Quaternary faults are discussed, and are included as potential earthquake generators. Earthquakes of appropriate magnitude to be assigned to each fault are determined by assuming rupture in one event of half the map length of the fault, and applying relations (determined by several authors) between earthquake magnitude and rupture length in historic events to determine magnitudes. These magnitudes are, for the purposes of this brief review, probably reasonable estimates of the capabilities of each fault, although earthquakes of larger magnitude are possible. Accelerations are then determined by assuming earthquakes of the above determined magnitude placed at the closest point to the site on the fault trace, and applying attenuation curves of three different authors. Considerable uncertainty is inherent in the rough estimates of seismic accelerations made herein, for they are dependent on a chain of judgments, each of which, in itself, is uncertain. Present knowledge of the geology of the region is incomplete, so that geometry and structural relations of the faults are in part uncertain, and much evidence bearing on the youth of the faults has yet to be gathered and evaluated. Estimation of earthquake magnitude is also uncertain, and even assuming that approximate magnitude is known rather than estimated from fault length, estimates of maximum ground acceleration may differ greatly depending on the authority used. Further consideration of ground acceleration at the site might refine the estimates made herein and resolve the apparent contradictions between the authorities cited. Attention to frequency and duration of strong shaking would also be appropriate. This study was undertaken at the request of A. J. Pressesky, Assistant Director for Nuclear Safety, Division of Reactor-Development and Technology, U.S. Atomic Energy Commission, in March, 1969. It is based on a brief review of pertinent literature to which the authors had immediate access during the few weeks (April-May, 1969) available for report preparation. Because the report is limited both in scope and thoroughness, it must be considered no more than a first estimate of the tectonic and seismic environment of the Burro Flats site, and should not be considered sufficient, in itself, as a basis for design. The report is intended, however, to indicate the breadth of inquiry that is necessary in the consideration of ground acceleration at sites in California, and to indicate the incomplete status of geologic mapping and other geologic studies in the region. The report describes the tectonic environment of the Burro Flats site, discusses 10 pertinent faults individually, and presents possible earthquake magnitudes for those faults and resultant potential ground accelerations at the site.

California

Geophysical logging For hydrogeology

Geophysical logging is the measurement and analysis of electrical, acoustic, nuclear, and other physical properties in a borehole using wireline or direct push technology. Geophysical logging is one of the primary methods of collecting subsurface information for hydrogeologic investigations. Groundwater scientists and engineers should have a basic understanding of borehole geophysics and how it is applied in the characterization of aquifer systems. In this book, the different types of geophysical logs and equipment used in hydrogeologic investigations are reviewed. Applications and analysis methods are illustrated by specific examples in both unconsolidated deposits and bedrock settings. Key references for further exploration of the methods and applications are provided. Hands-on exercises are included for students to develop and practice log-analysis skills.

Book

A science and technology initiative within the office of civilian radioactive waste management

In 2002, by following a national decision-making process that had been specified in the 1982 Nuclear Waste Policy Act, Yucca Mountain (YM) was designated as the site for the nation's geologic repository for commercial spent nuclear fuel (SNF). The U.S. Department of Energy's (DOE's) Office of Civilian Radioactive Waste Management (OCRWM) must now obtain regulatory approval to construct and operate a repository there, and to develop transportation and infrastructure needed to support operations. The OCRWM has also recently begun a separate Science and Technology (S&T) initiative, whose purposes, beginnings, current projects, and future plans are described here.

Conference Paper