SEARCH · Geology Reports

Results for “Waste Management”

Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

SourceResearch connectionFrom yearThrough year

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 73 records · Page 4Linked to original sources

USGS1988

Radionuclides in ground water at the Idaho National Engineering Laboratory, Idaho

Sampling for radionuclides in groundwater was conducted at the Idaho National Engineering Laboratory during September to November 5 1987. Water samples from 80 wells that obtain water from the Snake River Plain aquifer and 1 well that obtains water from a shallow, discontinuous perched-water body at the Radioactive Waste Management Complex were collected and analyzed for tritium, strontium-90, plutonium-238, plutonium-239, -240 (undivided), americium-241, cesium-137, cobalt-60, and potassium-40--a naturally occurring radionuclide. The groundwater samples were analyzed at the Idaho National Engineering Laboratory in Idaho. Tritium and strontium-90 concentrations ranged from below the reporting level to 80.6 +/-0.000005 and 193 +/-5x10 to the minus eight micrograms Ci/ml, respectively. Water from a disposal well at Test Area North--which has not been used to dispose of waste water since September 1972--contained 122 +/-9x10 to the minus eleven micrograms Ci/ml of plutonium-238, 500 +/-20x10 to the minus eleven of plutonium-239, -240 (undivided), 21 +/-4x10 to the minus eleven micrograms Ci/ml of americium-241, and 750 +/-20x10 to the minus eight micrograms Ci/ml cesium-137; the presence of these radionuclides was verified by resampling and reanalysis. The disposal well had 8.9 +/-0.0000009 micrograms Ci/ml of cobalt-60 on October 28, 1987, but cobalt-60 was not detected when the well was resampled on January 11, 1988. Potassium-40 concentrations were less than the reporting level in all wells. (USGS)

Open-File Report↗

USGS2000

Environmental Setting and Effects on Water Quality in the Great and Little Miami River Basins, Ohio and Indiana

The Great and Little Miami River Basins drain approximately 7,354 square miles in southwestern Ohio and southeastern Indiana and are included in the more than 50 major river basins and aquifer systems selected for water-quality assessment as part of the U.S. Geological Survey's National Water-Quality Assessment Program. Principal streams include the Great and Little Miami Rivers in Ohio and the Whitewater River in Indiana. The Great and Little Miami River Basins are almost entirely within the Till Plains section of the Central Lowland physiographic province and have a humid continental climate, characterized by well-defined summer and winter seasons. With the exception of a few areas near the Ohio River, Pleistocene glacial deposits, which are predominantly till, overlie lower Paleozoic limestone, dolomite, and shale bedrock. The principal aquifer is a complex buried-valley system of sand and gravel aquifers capable of supporting sustained well yields exceeding 1,000 gallons per minute. Designated by the U.S. Environmental Protection Agency as a sole-source aquifer, the Buried-Valley Aquifer System is the principal source of drinking water for 1.6 million people in the basins and is the dominant source of water for southwestern Ohio. Water use in the Great and Little Miami River Basins averaged 745 million gallons per day in 1995. Of this amount, 48 percent was supplied by surface water (including the Ohio River) and 52 percent was supplied by ground water. Land-use and waste-management practices influence the quality of water found in streams and aquifers in the Great and Little Miami River Basins. Land use is approximately 79 percent agriculture, 13 percent urban (residential, industrial, and commercial), and 7 percent forest. An estimated 2.8 million people live in the Great and Little Miami River Basins; major urban areas include Cincinnati and Dayton, Ohio. Fertilizers and pesticides associated with agricultural activity, discharges from municipal and industrial wastewater-treatment and thermoelectric plants, urban runoff, and disposal of solid and hazardous wastes contribute contaminants to surface water and ground water throughout the study area. Surface water and ground water in the Great and Little Miami River Basins are classified as very hard, calcium-magnesiumbicarbonate waters. The major-ion composition and hardness of surface water and ground water reflect extensive contact with the carbonate-rich soils, glacial sediments, and limestone or dolomite bedrock. Dieldrin, endrin, endosulfan II, and lindane are the most commonly reported organochlorine pesticides in streams draining the Great and Little Miami River Basins. Peak concentrations of the herbicides atrazine and metolachlor in streams commonly are associated with post-application runoff events. Nitrate concentrations in surface water average 3 to 4 mg/L (milligrams per liter) in the larger streams and also show strong seasonal variations related to application periods and runoff events. Ambient iron concentrations in ground water pumped from aquifers in the Great and Little Miami River Basins often exceed the U.S. Environmental Protection Agency Secondary Maximum Contaminant Level (300 micrograms per liter). Chloride concentrations are below aesthetic drinking-water guidelines (250 mg/L), except in ground water pumped from low-yielding Ordovician shale; chloride concentrations in sodium-chloriderich ground water pumped from the shale bedrock can exceed 1,000 mg/L. Some of the highest average nitrate concentrations in ground water in Ohio and Indiana are found in wells completed in the buried-valley aquifer; these concentrations typically are found in those parts of the sand and gravel aquifer that are not overlain by clay-rich till. Atrazine was the most commonly detected herbicide in private wells. Concentrations of volatile organic compounds in ground water generally were below Federal drinking-water standards, except near areas of known or suspected contamination. Evaluation of fish and macroinvertebrate community performance in streams and rivers draining the Great and Little Miami River Basins indicates that most streams meet basic aquatic-life-use criteria set by the Ohio Environmental Protection Agency for warmwater habitat. Stream reaches whose biological community performance meet aquatic-lifeuse criteria defined for exceptional warmwater habitat are found in Twin Creek, the Upper Great Miami River, the Little Miami River, and the Whitewater River Basins. Other streams have exhibited significant improvements in biological community performance (and water quality)'that are attributed primarily to reduced pollutant loadings from wastewater-treatment plants upgraded since 1972. Four hydrogeomorphic regions were delineated in the Great and Little Miami River Basins based on distinct and relatively homogeneous natural characteristics. Primary features used to delineate the hydrogeomorphic regions include bedrock geology, surficial geology, physiography, hydrology, soil types, and vegetation. These four regions Till Plains, Drift Plains/Unglaciated, Interlobate, and Fluvial are used in the Great and Little Miami River Basins study to assess the influence of natural features of the environmental setting on surface- and ground-water quality.

Indiana, Ohio↗

USGS2013

Water volume and sediment volume and density in Lake Linganore between Boyers Mill Road Bridge and Bens Branch, Frederick County, Maryland, 2012

To assist in understanding sediment loadings and the management of water resources, a bathymetric survey was conducted in the part of Lake Linganore between Boyers Mill Road Bridge and Bens Branch in Frederick County, Maryland. The bathymetric survey was performed in January 2012 by the U.S. Geological Survey, in cooperation with the City of Frederick and Frederick County. A separate, but related, field effort to collect 18 sediment cores was conducted in March and April 2012. Depth and location data from the bathymetric survey and location data for the sediment cores were compiled and edited by using geographic information system (GIS) software. A three-dimensional triangulated irregular network (TIN) model of the lake bottom was created to calculate the volume of stored water in the reservoir. Large-scale topographic maps of the valley prior to inundation in 1972 were provided by the Frederick County Division of Utilities and Solid Waste Management and digitized for comparison with current (2012) conditions in order to calculate sediment volume. Cartographic representations of both water depth and sediment accumulation were produced, along with an accuracy assessment for the resulting bathymetric model. Vertical accuracies at the 95-percent confidence level for the collected data, the bathymetric surface model, and the bathymetric contour map were calculated to be 0.64 feet (ft), 1.77 ft, and 2.30 ft, respectively. A dry bulk sediment density was calculated for each of the 18 sediment cores collected during March and April 2012, and used to determine accumulated sediment mass. Water-storage capacity in the study area is 110 acre-feet (acre-ft) at a full-pool elevation 308 ft above the National Geodetic Vertical Datum of 1929, whereas total sediment volume in the study area is 202 acre-ft. These totals indicate a loss of about 65 percent of the original water-storage capacity in the 40 years since dam construction. This corresponds to an average rate of sediment accumulation of 5.1 acre-ft per year since Linganore Creek was impounded. Sediment thicknesses ranged from 0 to 16.7 ft. Sediment densities ranged from 0.38 to 1.08 grams per cubic centimeter, and generally decreased in the downstream direction. The total accumulated-sediment mass was 156,000 metric tons between 1972 and 2012.

Maryl↗

USGS2013

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↗

USGS2005

Mercury recycling in the United States in 2000

Reclamation and recycling of mercury from used mercury- containing products and treatment of byproduct mercury from gold mining is vital to the continued, though declining, use of this metal. Mercury is reclaimed from mercury-containing waste by treatment in multistep high-temperature retorts-the mercury is volatized and then condensed for purification and sale. Some mercury-containing waste, however, may be landfilled, and landfilled material represents loss of a recyclable resource and a threat to the environment. Related issues include mercury disposal and waste management, toxicity and human health, and regulation of mercury releases in the environment. End-users of mercury-containing products may face fines and prosecution if these products are improperly recycled or not recycled. Local and State environmental regulations require adherence to the Resource Conservation and Recovery Act and the Comprehensive Environmental Response, Compensation, and Liability Act to regulate generation, treatment, and disposal of mercury-containing products. In the United States, several large companies and a number of smaller companies collect these products from a variety of sources and then reclaim and recycle the mercury. Because mercury has not been mined as a principal product in the United States since 1992, mercury reclamation from fabricated products has become the main source of mercury. Principal product mercury and byproduct mercury from mining operations are considered to be primary materials. Mercury may also be obtained as a byproduct from domestic or foreign gold-processing operations. In the early 1990s, U.S. manufacturers used an annual average that ranged from 500 to 600 metric tons of recycled and imported mercury for fabrication of automobile convenience switches, dental amalgam, fluorescent lamps, medical uses and thermometers, and thermostats. The amount now used for fabrication is estimated to be 200 metric tons per year or less. Much of the data on mercury is estimated because it is a low-volume commodity and its production, use, and disposal is difficult to track. The prices and volumes of each category of mercury-containing material may change dramatically from year to year. For example, the average price of mercury was approximately $150 per flask from 2000 until 2003 and then rose sharply to $650 per flask in fall 2004 and approximately $850 per flask in spring 2005. Since 1927, the common unit for measuring and pricing mercury has been the flask in order to conform to the system used at Almaden, Spain (Meyers, 1951). One flask weighs 34.5 kilograms, and 29 flasks of mercury are contained in a metric ton. In the United States, the chlorine-caustic soda industry, which is the leading end-user of elemental mercury, recycles most of its mercury in-plant as home scrap. Annual purchases of replacement mercury by the chlorine-caustic soda industry indicate that some mercury may be lost through evaporation to the environment, put into a landfill as industrial waste, or trapped within pipes in the plant. Impending closure of domestic and foreign mercury-cell chlorine-caustic soda plants and the shift to nonmercury technology for chlorine-caustic soda production could ultimately result in a significant volume of elemental mercury for recycling, sale, or storage. Globally, mercury is widely used in artisanal, or small-scale, gold mining. Most of that mercury is lost to the environment and is not recycled. The recycling rate for mercury was not available owing to insufficient data in 2000, and the efficiency of mercury recycling was estimated to be 62 percent.

Circular↗

USGS2005

Mercury recycling in the United States in 2000

Open-File Report↗

USGS2015

Water-quality characteristics and trends for selected wells possibly influenced by wastewater disposal at the Idaho National Laboratory, Idaho, 1981-2012

The U.S. Geological Survey, in cooperation with the U.S. Department of Energy, analyzed water-quality data collected from 64 aquifer wells and 35 perched groundwater wells at the Idaho National Laboratory (INL) from 1981 through 2012. The wells selected for the study were wells that possibly were affected by wastewater disposal at the INL. The data analyzed included tritium, strontium-90, major cations, anions, nutrients, trace elements, total organic carbon, and volatile organic compounds. The analyses were performed to examine water-quality trends that might influence future management decisions about the number of wells to sample at the INL and the type of constituents to monitor. The data were processed using custom computer scripts developed in the R programming language. Summary statistics were calculated for the datasets. Water-quality trends were determined using a parametric survival regression model to fit the observed data, including left-censored, interval-censored, and uncensored data. The null hypothesis of the trend test was that no relation existed between time and concentration; the alternate hypothesis was that time and concentration were related through the regression equation. A significance level of 0.05 was selected to determine if the trend was statistically significant. Trend test results for tritium and strontium-90 concentrations in aquifer wells indicated that nearly all wells had decreasing or no trends. Similarly, trends in perched groundwater wells were mostly decreasing or no trends; trends were increasing in two perched groundwater wells near the Advanced Test Reactor Complex. Decreasing trends generally are attributed to lack of recent wastewater disposal and radioactive decay. Trend test results for chloride, sodium, sulfate, nitrite plus nitrate (as nitrogen), chromium, trace elements, and total organic carbon concentrations in aquifer wells indicated that most wells had either decreasing or no trends. The decreasing trends in these constituents are attributed to decrease in disposal of these constituents, as well as discontinued use of the old percolation ponds south of the Idaho Nuclear Technology and Engineering Center (INTEC) and redirection of wastewater to the new percolation ponds 2 miles southwest of the INTEC in 2002. Chloride (along with sodium, sulfate, and some nitrate) concentrations in wells south of the INTEC may be influenced by episodic recharge from the Big Lost River. These constituent concentrations decrease during wetter periods when there is probably more recharge from the Big Lost River and increase during dry periods, when there is less recharge. Some wells downgradient of the Central Facilities Area and near the southern boundary of the INL showed increasing trends in sodium concentration, whereas there was no trend in chloride. The increasing trend for sodium could be due to the long term influence of wastewater disposal from upgradient facilities and the lack of trend for chloride could be because chloride is more mobile than sodium and more dispersed in the aquifer system. Volatile organic compound concentration trends were analyzed for nine aquifer wells. Trend test results indicated an increasing trend for carbon tetrachloride for the Radioactive Waste Management Complex Production Well for the period 1987–2012; however, trend analyses of data collected since 2005 show no statistically significant trend indicating that engineering practices designed to reduce movement of volatile organic compounds to the aquifer may be having a positive effect on the aquifer.

Idaho↗

USGS2013

Can shale safely host US nuclear waste?

"Even as cleanup efforts after Japan’s Fukushima disaster offer a stark reminder of the spent nuclear fuel (SNF) stored at nuclear plants worldwide, the decision in 2009 to scrap Yucca Mountain as a permanent disposal site has dimmed hope for a repository for SNF and other high-level nuclear waste (HLW) in the United States anytime soon. About 70,000 metric tons of SNF are now in pool or dry cask storage at 75 sites across the United States [Government Accountability Office, 2012], and uncertainty about its fate is hobbling future development of nuclear power, increasing costs for utilities, and creating a liability for American taxpayers [Blue Ribbon Commission on America’s Nuclear Future, 2012].However, abandoning Yucca Mountain could also result in broadening geologic options for hosting America’s nuclear waste. Shales and other argillaceous formations (mudrocks, clays, and similar clay-rich media) have been absent from the U.S. repository program. In contrast, France, Switzerland, and Belgium are now planning repositories in argillaceous formations after extensive research in underground laboratories on the safety and feasibility of such an approach [Blue Ribbon Commission on America’s Nuclear Future, 2012; Nationale Genossenschaft für die Lagerung radioaktiver Abfälle (NAGRA), 2010; Organisme national des déchets radioactifs et des matières fissiles enrichies, 2011]. Other nations, notably Japan, Canada, and the United Kingdom, are studying argillaceous formations or may consider them in their siting programs [Japan Atomic Energy Agency, 2012; Nuclear Waste Management Organization (NWMO), (2011a); Powell et al., 2010]."

Eos, Transactions, American Geophysical Union↗

USGS1987

Stratification of a cityscape using census and land use variables for inventory of building materials

A cityscape (or any landscape) can be stratified into environmental units using multiple variables of information. For the purposes of sampling building materials, census and land use variables were used to identify similar strata. In the Metropolitan Statistical Area of a cityscape, the census tract is the smallest unit for which census data are summarized and digitized boundaries are available. For purposes of this analysis, census data on total population, total number of housing units, and number of singleunit dwellings were aggregated into variables of persons per square kilometer and proportion of housing units in single-unit dwellings. The level 2 categories of the U.S. Geological Survey's land use and land cover data base were aggregated into variables of proportion of residential land with buildings, proportion of nonresidential land with buildings, and proportion of open land. The cityscape was stratified, from these variables, into environmental strata of Urban Central Business District, Urban Livelihood Industrial Commercial, Urban Multi-Family Residential, Urban Single Family Residential, Non-Urban Suburbanizing, and Non-Urban Rural. The New England region was chosen as a region with commonality of building materials, and a procedure developed for trial classification of census tracts into one of the strata. Final stratification was performed by discriminant analysis using the trial classification and prior probabilities as weights. The procedure was applied to several cities, and the results analyzed by correlation analysis from a field sample of building materials. The methodology developed for stratification of a cityscape using multiple variables has application to many other types of environmental studies, including forest inventory, hydrologic unit management, waste disposal, transportation studies, and other urban studies. Multivariate analysis techniques have recently been used for urban stratification in England. ?? 1987 Annals of Regional Science.

The Annals of Regional Science↗

USGS2012

Models, validation, and applied geochemistry: Issues in science, communication, and philosophy

Models have become so fashionable that many scientists and engineers cannot imagine working without them. The predominant use of computer codes to execute model calculations has blurred the distinction between code and model. The recent controversy regarding model validation has brought into question what we mean by a ‘model’ and by ‘validation.’ It has become apparent that the usual meaning of validation may be common in engineering practice and seems useful in legal practice but it is contrary to scientific practice and brings into question our understanding of science and how it can best be applied to such problems as hazardous waste characterization, remediation, and aqueous geochemistry in general. This review summarizes arguments against using the phrase model validation and examines efforts to validate models for high-level radioactive waste management and for permitting and monitoring open-pit mines. Part of the controversy comes from a misunderstanding of ‘prediction’ and the need to distinguish logical from temporal prediction. Another problem stems from the difference in the engineering approach contrasted with the scientific approach. The reductionist influence on the way we approach environmental investigations also limits our ability to model the interconnected nature of reality. Guidelines are proposed to improve our perceptions and proper utilization of models. Use of the word ‘validation’ is strongly discouraged when discussing model reliability.

Applied Geochemistry↗

USGS2025

Component identification of solid biomass fuels using reflected light microscopy: Interlaboratory study 2

As nations transition toward sustainable energy systems , biomass has become a vital component of global energy portfolios. Derived from organic materials such as wood, agricultural residues, forestry byproducts, and organic waste, biomass is a renewable energy source with significant environmental and economic benefits. Responsible biomass energy production can improve waste management, reduce emissions of greenhouse gases, and mitigate environmental pollution. However, as the diversity of biomass-derived fuels increases, robust quality assessment methods are essential to ensure their efficiency, safety, and minimal environmental impact. Reflected light microscopy (RLM) is one such technique with the potential to complement conventional physico-chemical analyses by enabling a rapid identification of material constituents and impurities. To refine this methodology and evaluate the reproducibility of solid biomass component identification using RLM, an interlaboratory study (ILS) was conducted. The study involved the recognition of 58 components across 45 photomicrographs, with the participation of 65 scientists and students from 25 countries. The participants faced high difficulty identifying some of the marked components, and as a result, the percentage of correct answers ranged from 19.0 % to 98.3 %, with an average correct identification rate of 62.7 %. The most challenging aspects of the identification process included distinguishing between woody and non-woody (agro) biomass, accurately identifying petroleum-derived materials, and differentiating agro biomass from inorganic matter. The results suggest that while RLM is an important tool for characterizing solid biomass, further development of methodology guidelines and training are necessary to enhance its effectiveness. Future research should prioritize preparing detailed, image-rich, microscopic morphological descriptions of biomass fuel components, which could improve the accuracy and reliability of using RLM in biomass fuel characterization.

International Journal of Coal Geology↗

USGS2018

Mapping elemental contamination on Palmyra Atoll National Wildlife Refuge

Palmyra Atoll, once a WWII U.S. Navy air station, is now a U.S. National Wildlife Refuge with nearly 50 km 2 of coral reef and 275 ha of emergent lands with forests of Pisonia grandis trees and colonies of several bird species. Due to the known elemental and organic contamination from chemicals associated with aviation, power generation and transmission, waste management, and other air station activities, a screening survey to map elemental concentrations was conducted. A map of 1944 Navy facilities was georeferenced and identifiable features were digitized. These data informed a targeted survey of 25 elements in soils and sediment at locations known or suspected to be contaminated, using a hand-held X-ray fluorescence spectrometer. At dozens of locations, concentrations of elements exceeded established soil and marine sediment thresholds for adverse ecological effects. Results were compiled into a publicly available geospatial dataset to inform potential remediation and habitat restoration activities.

Marine Pollution Bulletin↗

USGS2019

Nearshore survey and cleanup of benthic marine debris using citizen science divers along the Mediterranean coast of Israel

Information on marine debris along the Mediterranean coast of Israel, especially on the seafloor, is limited. Many recreational divers are enthusiasts of marine conservation and can thus contribute to data collection which does not require highly specialized training. The Society for the Protection of Nature in Israel together with The Israeli Diving Federation established the diver volunteer program “Sea Guard” (“Mishmar Hayam” in Hebrew), which supports marine conservation through citizen science. The divers were trained in marine ecology and survey methods to conduct independent surveys and lead underwater cleanups. For the first time, we have described the patterns of benthic debris density and composition in the nearshore environment of the southeastern part of the Mediterranean Sea. We found that benthic marine debris in the nearshore along the Israeli Mediterranean coast is primarily plastic, likely originating from the use of local beaches. Fishing, boating and domestic activities also play an important role as sources for marine debris. The currents' regime prevented the debris from accumulating on the seafloor in the nearshore environment, with the exception of several “debris traps”. Our findings will be useful for the development of programs to improve coastal waste management.

Ocean and Coastal Management↗

USGS2021

Geochemical and geophysical indicators of oil and gas wastewater can trace potential exposure pathways following releases to surface waters

Releases of oil and gas (OG) wastewaters can have complex effects on stream-water quality and downstream organisms, due to sediment-water interactions and groundwater/surface water exchange. Previously, elevated concentrations of sodium (Na), chloride (Cl), barium (Ba), strontium (Sr), and lithium (Li), and trace hydrocarbons were determined to be key markers of OG wastewater releases when combined with Sr and radium (Ra) isotopic compositions. Here, we assessed the persistence of an OG wastewater spill in a creek in North Dakota using a combination of geochemical measurements and modeling, hydrologic analysis, and geophysical investigations. OG wastewater comprised 0.1 to 0.3% of the stream-water compositions at downstream sites in February and June 2015 but could not be quantified in 2016 and 2017. However, OG-wastewater markers persisted in sediments and pore water for 2.5 years after the spill and up to 7.2-km downstream from the spill site. Concentrations of OG wastewater constituents were highly variable depending on the hydrologic conditions. Electromagnetic measurements indicated substantially higher electrical conductivity under the bank adjacent to a seep 7.2 km downstream from the spill site. Geomorphic investigations revealed mobilization of sediment is an important contaminant transport process. Labile Ba, Ra, Sr, and ammonium (NH 4 ) concentrations extracted from sediments indicated sediments are a long-term reservoir of these constituents, both in the creek and on the floodplain. Using the drivers of ecological effects identified at this intensively studied site we identified 41 watersheds across the North Dakota landscape that may be subject to similar episodic inputs from OG wastewater spills. Effects of contaminants released to the environment during OG waste management activities remain poorly understood; however, analyses of Ra and Sr isotopic compositions, as well as trace inorganic and organic compound concentrations at these sites in pore-water provide insights into potentials for animal and human exposures well outside source-remediation zones.

North Dakota↗

USGS2025

Spatially resolved source apportionment of per- and polyfluoroalkyl substances (PFAS) within a post-industrial river catchment

Source apportionment of per- and polyfluoroalkyl substances (PFAS) in rivers is typically based on water concentrations, which cannot quantify PFAS loads or define geographical source areas. This study applied a river catchment-scale approach to identify PFAS source zones and assess the relative importance of industrial PFAS sources in the River Mersey, UK – a post-industrial, densely populated catchment with diverse PFAS sources. Synoptic sampling and PFAS river load analysis identified key sub-catchments and river stretches contributing the majority of PFAS. Notably, the highest PFAS concentrations did not always correspond to the greatest loads. Most PFOS (64 %), PFOA (49 %), 6:2FTS (46 %) and PFHxS (56 %) were exported from the Upper Mersey sub-catchment, despite higher concentrations in northern sub-catchments, emphasising the importance of load-based monitoring. Mass balance analysis of loads highlighted substantial inputs from specific river stretches, notably the Lower Irwell (Bolton to Manchester City Centre), River Tame (Marple Bridge to Stockport), and Upper Mersey (Stockport to Urmston). While PFAS loads generally scaled with catchment area, yield (load per unit area) analysis identified disproportionately high exports from small headwater catchments, notably the upper River Roch (PFOA, PFHpA and PFHxA) and Glaze Brook (PFBS). Industrial sources in these sub-catchments (a waste management facility and landfills, respectively) were confirmed using gadolinium anomaly analysis and consented discharge records. More widely, gadolinium data suggested industrial discharges may contribute to PFAS occurrence at 62 % of our sample sites throughout the catchment. These findings demonstrate that spatial analysis of PFAS loads, rather than concentrations alone, is critical for identifying PFAS source areas. We present a scalable monitoring framework for PFAS source apportionment applied at the river catchment-scale that can be used by environmental managers to target and prioritise PFAS source areas for detailed monitoring and remediation.

River Mersey↗

USGS2010

Use and environmental occurrence of pharmaceuticals in freestall dairy farms with manured forage fields

Environmental releases of antibiotics from concentrated animal feeding operations (CAFOs) are of increasing regulatory concern. This study investigates the use and occurrence of antibiotics in dairy CAFOs and their potential transport into first-encountered groundwater. On two dairies we conducted four seasonal sampling campaigns, each across 13 animal production and waste management systems and associated environmental pathways: application to animals, excretion to surfaces, manure collection systems, soils, and shallow groundwater. Concentrations of antibiotics were determined using on line solid phase extraction (OLSPE) and liquid chromatography-tandem mass spectrometry (LC/MS/MS) with electrospray ionization (ESI) for water samples, and accelerated solvent extraction (ASE) LC/MS/MS with ESI for solid samples. A variety of antibiotics were applied at both farms leading to antibiotics excretion of several hundred grams per farm per day. Sulfonamides, tetracyclines, and their epimers/isomers, and lincomycin were most frequently detected. Yet, despite decades of use, antibiotic occurrence appeared constrained to within farm boundaries. The most frequent antibiotic detections were associated with lagoons, hospital pens, and calf hutches. When detected below ground, tetracyclines were mainly found in soils, whereas sulfonamides were found in shallow groundwater reflecting key differences in their physicochemical properties. In manure lagoons, 10 compounds were detected including tetracyclines and trimethoprim. Of these 10, sulfadimethoxine, sulfamethazine, and lincomycin were found in shallow groundwater directly downgradient from the lagoons. Antibiotics were sporadically detected in field surface samples on fields with manure applications, but not in underlying sandy soils. Sulfadimethoxine and sulfamethazine were detected in shallow groundwater near field flood irrigation gates, but at highly attenuated levels.

Environmental Science & Technology↗

USGS2003

Mobilization of radionuclides from uranium mill tailings and related waste materials in anaerobic environments

Specific extraction studies in our laboratory have shown that iron and manganese oxide- and alkaline earth sulfate minerals are important hosts of radium in uranium mill tailings. Iron- and sulfate-reducing bacteria may enhance the release of radium (and its analog barium) from uranium mill tailings, oil field pipe scale [a major technologically enhanced naturally occurring radioactive material (TENORM) waste], and jarosite (a common mineral in sulfuric acid processed-tailings). These research findings are reviewed and discussed in the context of nuclear waste forms (such as barium sulfate matrices), radioactive waste management practices, and geochemical environments in the Earth's surficial and shallow subsurface regions.

Journal of Radioanalytical and Nuclear Chemistry↗

USGS2022

Pharmaceutical pollution of the world’s rivers

Environmental exposure to active pharmaceutical ingredients (APIs) can have negative effects on the health of ecosystems and humans. While numerous studies have monitored APIs in rivers, these employ different analytical methods, measure different APIs, and have ignored many of the countries of the world. This makes it difficult to quantify the scale of the problem from a global perspective. Furthermore, comparison of the existing data, generated for different studies/regions/continents, is challenging due to the vast differences between the analytical methodologies employed. Here, we present a global-scale study of API pollution in 258 of the world’s rivers, representing the environmental influence of 471.4 million people across 137 geographic regions. Samples were obtained from 1,052 locations in 104 countries (representing all continents and 36 countries not previously studied for API contamination) and analyzed for 61 APIs. Highest cumulative API concentrations were observed in sub-Saharan Africa, south Asia, and South America. The most contaminated sites were in low- to middle-income countries and were associated with areas with poor wastewater and waste management infrastructure and pharmaceutical manufacturing. The most frequently detected APIs were carbamazepine, metformin, and caffeine (a compound also arising from lifestyle use), which were detected at over half of the sites monitored. Concentrations of at least one API at 25.7% of the sampling sites were greater than concentrations considered safe for aquatic organisms, or which are of concern in terms of selection for antimicrobial resistance. Therefore, pharmaceutical pollution poses a global threat to environmental and human health, as well as to delivery of the United Nations Sustainable Development Goals.

Proceedings of the National Academy of Sciences↗