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USGS1981

Water Resources Research October 1, 1979 - September 30, 1980: Summary statements of research activities by the Water Resources Division

Research in the WRD had its beginnings in the late 1950's when the "core research" line item was added to the Congressional budget. Since this time the Federal program has grown from a "basic sciences" program to one that includes a broad spectrum of basic and applied scientific investigations. Water resources research in WRD includes the study of water in all its phases and uses the basic sciences of mathematics, chemistry, physics, biology, geology and engineering to gain a fundamental understanding of the processes that affect the movement of water and its chemical constituents through hydrologic systems. The basic knowledge and methodologies derived from water resources research are applicable not only to the solution of current problems associated with the Nation's water resources, but also to anticipated hydrologic issues.

Report↗

USGS1978

Comparison of the Wilfley concentration table and hand panning for concentration of heavy minerals prior to geochemical analysis

Chemical analysis of heavy—mineral concentrates of stream sediments is a common geochemical exploration technique used by the U.S. Geological Survey. Generally these concentrates are prepared by hand panning at streamside or in a washtub and then further concentrated using heavy—liquid (bromoform) techniques in a laboratory. Concentration using heavy liquids is slow, tedious, and expensive for large surveys such as mineral evaluation of wilderness areas. In addition the cost of bromoform is expected to increase greatly because most if not all chemical companies in the United States have ceased production of the compound due to problems in meeting the safety standards of the U.S. Environmental Protection Agency (E.P.A.). Preliminary studies by the E.P.A. suggest a severe health hazard may be incurred by inhaling vapors of or contacting the skin with chemicals like bromoform. Heavy—liquid concentration of thousands of heavy— mineral samples carries an unavoidable risk of exposure to bromoform. The risk, expense, and time required by routine heavy—liquid concentration of heavy minerals should be eliminated by finding other methods to satisfactorily concentrate minerals whenever it is possible. Heavy—mineral concentrates can be used in several ways in geochemical exploration and each way has certain standards for the nature and quality of the mineral concentration required. The nature of the concentration refers to whether the heavy minerals are analyzed in bulk or whether they are split into magnetic fractions using a hand magnet and possibly a Frantz Isodynamic Magnetic Separator.

Open-File Report↗

USGS1978

Spectrographic and chemical analyses of whole-rock and insoluble-residue samples, Rolla 1 degree x 2 degrees quadrangle, Missouri: Drill holes no. 18, 19, and 20

Geochemical studies of the Rolla, Mo., 1° x 2° quadrangle were begun in 1977 as part of a joint multidisciplinary study of the quadrangle by the U.S. Geological Survey and the Division of Geology and Land Survey, Missouri Department of Natural Resources. The study is to access the mineral resource potential of the area by integrated geologic, geochemical, and geophysical studies. The geochemical work to date has been directed at the characterization of the sedimentary and igneous rocks in the quadrangle through spectrographic and chemical analyses of whole-rock samples and dilute-hydrochloric-acid insoluble-residue samples of whole rock from widely spaced drill holes. Sixty-two drill holes have been selected for study from the sample library of the Missouri Division of Geology and Land Survey. None of the holes are company-confidential, none intersect economically significant mineralized ground, and only a few are located in known ore-bearing trends. The analytical results for drill hole no. 18, Missouri log numbers 24244 and 20974, drill hole no. 19, Missouri log numbers 20967 and 23863, and for drill hole no. 20, Missouri log number 20154, are given in this report. Drill hole no. 18 is located in sec. 13, T. 33 N., R. 1 W., in Reynolds County, drill hole no. 19 is located in sec. 2, T. 34 N., R. 1 W. in Iron County, and drill hole no. 20 is located in sec. 16, T. 35 N., R. 1 W. in Washington County. Data for the whole-rock samples for drill hole no. 18 are listed in table 1, and data for the insoluble-residue samples for drill hole no. 18 are listed in table 2.

Missouri↗

USGS1997

Characterization of springflow in the north coast limestone of Puerto Rico using physical, chemical, and stable isotopic methods

The carbonate sequence of middle Tertiary age of the north coast of Puerto Rico is characterized by the presence of numerous springs in the coastal areas. In order to advance the understanding of the hydrologic role of the springs in the north coast limestone aquifer system of Puerto Rico, a 4-year study was conducted by the U.S. Geological Survey in cooperation with the Puerto Rico Aqueduct and Sewer Authority. As part of this study, data were collected on the chemical, physical, bacteriological, oxygen-18, and deuterium composition of water from springs in the Dorado to Rincon area, in northwestern Puerto Rico. A group of springs in the Dorado to Arecibo area was selected for more detailed monitoring. Oxygen-18 and deuterium composition was also determined for water wells and monthly rainfall composites at a series of sites in the study area. Springs are associated with all the carbonate units of the middle Tertiary sequence of the northern karst belt of Puerto Rico, except the Camuy and San Sebastian Formations. These springs mostly drain the unconfined parts of the upper and lower aquifers in the north coast limestone aquifer system. There are no first and second order springs in the north coast limestone and of those present fifth and sixth order springs are the most numerous type. Springflow at the springs measured during the study ranged from less than 0.1 to 61 cubic feet per second. Springs in the north coast limestone can also be classified by their response to rainfall. There is little or no short-term response to rainfall at springs such as Ojo de Agua in Vega Baja, Mameyes in Manati, and Mackovic in Vega Alta. These springs are known as diffuse-type springs. Other springs such as Maguayo in Dorado, Ojo de Guillo in Manati, and San Pedro in Arecibo exhibit a strong short-term response to rainfall and are known as conduit-type springs. Spring water temperature, during the study, ranged from 22.5 to 28 °C and resembled air temperature. Specific conductance ranged from 289 to about 4,000 microsiemens per centimeter, and pH ranged from 6.9 to 7.8. Calcium, sodium, bicarbonate, and chloride are the main ionic species in water from the springs sampled during the study. The main water type is calcium-bicarbonate and secondary water types are calcium-bicarbonate chloride and sodium-bicarbonate-chloride. A seasonal and short-term transient relation exists, particularly in conduit-type springs, between springflow, physical properties, and water quality. Temporal and spatial variations in the oxygen-18 and deuterium composition of modern precipitation are significantly larger than those of springs and ground water in the study area. Regional flow in the upper aquifer appears to attenuate or average the variations in isotopic composition of rainfall. There is, however, a regional gradient in the deuterium composition of water from the upper aquifer in the north coast limestone, with isotopically heavier water occurring further north. It was possible to determine the source of water contributing to springs at some sites with more detailed data collection and analysis. A drainage basin of about 10 square kilometers was delineated for the Ojo de Agua spring in Vega Baja, for a base flow of 2 cubic feet per second and an estimated subregional recharge rate of around 20 inches per year. A delineation of drainage basins for conduit-type springs in the study area such as San Pedro, Ojo de Guillo, Maguayo, and others is very difficult because the boundaries of these systems are highly responsive to changing hydraulic conditions such as rapid and short-term variations in the hydraulic head distribution as a consequence of rainfall. However, a preliminary drainage basin of about 6 square kilometers was delineated for the San Pedro spring for a base flow of 2 cubic feet per second and an estimated subregional annual recharge of 12 inches.

Puerto Rico↗

USGS1986

Hydrologic, lithologic, and chemical data for sediment in the shallow alluvial aquifer at two sites near Fallon, Churchill County, Nevada, 1984-85

The U.S. Geological Survey collected an extensive amount of hydrogeologic data from the shallow alluvial aquifer at two study sites near Fallon, Nevada, from 1984 though 1985. These data were collected as part of a study to determine the geochemical controls on the mobility of arsenic and other trace elements in shallow groundwater systems. The main study area is approximately 7 miles south of Fallon. A subsidiary study area is about 8 miles east of Fallon. The data collected include lithologic logs and water level altitudes for the augered sampling wells and piezometers, and determinations of arsenic and selenium content, grain size, porosity, hydraulic conductivity, and mineralogy for sediment samples from cores. (USGS)

Open-File Report↗

USGS1996

Methods of analysis by the U.S. Geological Survey National Water Quality Laboratory-Preparation procedure for aquatic biological material determined for trace metals

A method for the chemical preparation of tissue samples that are subsequently analyzed for 22 trace metals is described. The tissue-preparation procedure was tested with three National Institute of Standards and Technology biological standard reference materials and two National Water Quality Laboratory homogenized biological materials. A low-temperature (85 degrees Celsius) nitric acid digestion followed by the careful addition of hydrogen peroxide (30-percent solution) is used to decompose the biological material. The solutions are evaporated to incipient dryness, reconstituted with 5 percent nitric acid, and filtered. After filtration the solutions were diluted to a known volume and analyzed by inductively coupled plasma-mass spectrometry (ICP-MS), inductively coupled plasma-atomic emission spectrometry (ICP-AES), and cold vapor-atomic absorption spectrophotometry (CV-AAS). Many of the metals were determined by both ICP-MS and ICP-AES. This report does not provide a detailed description of the instrumental procedures and conditions used with the three types of instrumentation for the quantitation of trace metals determined in this study. Statistical data regarding recovery, accuracy, and precision for individual trace metals determined in the biological material tested are summarized.

Open-File Report↗

USGS2013

Fate(s) of injected CO2 in a coal-bearing formation, Louisiana, Gulf Coast Basin: Chemical and isotopic tracers of microbial-brine-rock-CO2 interactions

Coal beds are one of the most promising reservoirs for geologic carbon dioxide (CO₂) sequestration, as CO₂ can strongly adsorb onto organic matter and displace methane; however, little is known about the long-term fate of CO₂ sequestered in coal beds. The "2800' sand" of the Olla oil field is a coal-bearing, oil and gas-producing reservoir of the Paleocene–Eocene Wilcox Group in north-central Louisiana. In the 1980s, this field, specifically the 2800' sand, was flooded with CO₂ in an enhanced oil recovery (EOR) project, with 9.0×10⁷m³ of CO₂ remaining in the 2800' sand after injection ceased. This study utilized isotopic and geochemical tracers from co-produced natural gas, oil and brine from reservoirs located stratigraphically above, below and within the 2800' sand to determine the fate of the remaining EOR-CO₂, examining the possibilities of CO₂ migration, dissolution, mineral trapping, gas-phase trapping, and sorption to coal beds, while also testing a previous hypothesis that EOR-CO₂ may have been converted by microbes (CO₂-reducing methanogens) into methane, creating a microbial "hotspot". Reservoirs stratigraphically-comparable to the 2800' sand, but located in adjacent oil fields across a 90-km transect were sampled to investigate regional trends in gas composition, brine chemistry and microbial activity. The source field for the EOR-CO₂, the Black Lake Field, was also sampled to establish the δ¹³C-CO₂ value of the injected gas (0.9‰ +/- 0.9‰). Four samples collected from the Olla 2800' sand produced CO₂-rich gas with δ¹³C-CO₂ values (average 9.9‰) much lower than average (pre-injection) conditions (+15.9‰, average of sands located stratigraphically below the 2800' sand in the Olla Field) and at much higher CO₂ concentrations (24.9 mole %) than average (7.6 mole %, average of sands located stratigraphically below the 2800' sand in the Olla Field), suggesting the presence of EOR-CO₂ and gas-phase trapping as a major storage mechanism. Using δ¹³C values of CO₂ and dissolved organic carbon (DIC), CO₂ dissolution was also shown to be a major storage mechanism for 3 of the 4 samples from the Olla 2800' sand. Minor storage mechanisms were shown to be migration, which only affected 2 samples (from 1 well), and some EOR-CO₂ conversion to microbial methane for 3 of the 4 Olla 2800' sand samples. Since methanogenesis was not shown to be a major storage mechanism for the EOR-CO₂ in the Olla Field (CO₂ injection did not stimulate methanogenesis), samples were examined from adjacent oil fields to determine the cause of the Olla microbial "hot-spot". Microbial methane was found in all oil fields sampled, but indicators of methanogenesis (e.g. alkalinity, high δ¹³C-DIC values) were the greatest in the Olla Field, and the environmental conditions (salinity, pH, temperature) were most ideal for microbial CO₂ reduction in the Olla field, compared to adjacent fields.

Thesis↗

USGS2019

Drinking water health standards comparison and chemical analysis of groundwater for 72 domestic wells in Bradford County, Pennsylvania, 2016

Pennsylvania has the second highest number of residential wells of any state in the Nation with approximately 2.4 million residents that depend on groundwater for their domestic water supply. Despite the widespread reliance on groundwater in rural areas of the state, publicly available data to characterize the quality of private well water are limited. In Bradford County, more than half of the residents use groundwater from private domestic-supply wells as their primary drinking source. The quality of private well water is influenced by the regional and local setting, including the surrounding soil, geology, land use, household plumbing, and well construction. The groundwater used for domestic water supply in Bradford County is obtained primarily from shallow bedrock and from unconsolidated (glacial) deposits that overlie the bedrock. Historical land use has been predominately forested, agricultural, and residential, but more recently unconventional oil/gas development has been distributed throughout the landscape. Pennsylvania is one of only two states in the Nation without statewide water-well construction standards. To better assess the quality of groundwater used for drinking water supply in Bradford County, data for 72 domestic wells were collected and analyzed for a wide range of constituents that could be evaluated in relation to drinking water health standards, geology, land use, and other environmental factors. Groundwater samples were collected from May through August 2016 and analyzed for physical and chemical properties, including major ions, nutrients, trace elements, volatile organic compounds, ethylene and propylene glycol, alcohols, gross-alpha/beta-particle activity, uranium, radon-222, and dissolved gases. A subset of samples was analyzed for radium isotopes (radium-226 and -228) and for the isotopic composition of methane. This study was conducted by the U.S. Geological Survey in cooperation with the Northern Tier Regional Planning and Development Commission and is part of a regional effort to characterize groundwater in rural areas of Pennsylvania. Results of the 2016 study show that groundwater quality generally met most drinking-water standards. However, a percentage of samples failed to meet maximum contaminant levels (MCLs) for total coliform bacteria (49.3 percent), Escherichia coli (8.5 percent), barium (2.8 percent), and arsenic (2.8 percent); and secondary maximum contaminant levels (SMCL) for sodium (48.6 percent), manganese (30.6 percent), gross alpha and beta activity (16.7 percent), iron (11.1 percent), pH (8.3 percent), total dissolved solids (5.6 percent), chloride (1.4 percent), and aluminum (1.4 percent). Radon-222 activities exceeded the proposed drinking-water standard of 300 picocuries per liter (pCi/L) in 70.4 percent of the samples. There were no exceedances of drinking water health standards for any volatile organic compounds, and the only detections were for three trihalomethanes in one sample. The pH of the groundwater had a large influence on chemical characteristics and ranged from 6.18 to 9.31. Generally, the higher pH samples had higher potential for elevated concentrations of several constituents, including total dissolved solids, sodium, lithium, chloride, fluoride, boron, arsenic, and methane. For the Bradford County well-water samples, calcium/bicarbonate type waters were most abundant, with others classified as sodium/bicarbonate or mixed water types including calcium-sodium/bicarbonate, calcium-sodium/bicarbonate-chloride, sodium/bicarbonate-chloride, sodium/bicarbonate-sulfate, or sodium/chloride types. Six principal components (pH, redox, hardness, chloride-bromide, strontium-barium, and molybdenum-arsenic) explained nearly 78.3 percent of the variance in the groundwater dataset. Groundwater from 12.5 percent of the wells had concentrations of methane greater than the Pennsylvania action level of 7 milligrams per liter (mg/L); detectable methane concentrations ranged from 0.01 to 77 mg/L. In addition, low levels of ethane (as much as 0.13 mg/L) were present in seven samples with the highest methane concentrations. The isotopic composition of methane in five of these groundwater samples was consistent with the isotopic compositions reported for mud-gas logging samples from these geologic units and a thermogenic source. Isotopic composition from a sixth sample suggested the methane in that sample may be of microbial origin. Well-water samples with the higher methane concentrations also had higher pH values and elevated concentrations of sodium, lithium, boron, fluoride, arsenic, and bromide. Relatively elevated concentrations of some other constituents, such as barium and chloride, commonly were present in, but not limited to, those well-water samples with elevated methane. Four of the six groundwater samples with the highest methane concentrations had chloride/bromide ratios that indicate mixing with a small amount of brine (0.02 percent or less) similar in composition to those reported for gas and oil well brines in Pennsylvania. In several other eastern Pennsylvania counties where gas drilling is absent, groundwater with comparable chloride/bromide ratios and chloride concentrations have been reported, implying a potential natural source of brine. Most of Bradford County well-water samples have chloride concentrations less than 20 mg/L, and those with higher chloride concentrations have chloride/bromide ratios that indicate anthropogenic sources (such as road-deicing salt and septic effluent) or brine. Brines that are naturally present may originate from deeper parts of the aquifer system, whereas anthropogenic sources are more likely to affect shallow groundwater because they occur on or near the land surface. The available data for this study indicate that no one physical factor, such as the topographic setting, well depth, or altitude at the bottom of the well, was particularly useful for predicting those well locations with an elevated dissolved concentration of methane. The 2016 assessment of groundwater quality in Bradford County shows groundwater is generally of good quality, but methane and some constituents that occur in high concentration in naturally occurring brine and also in produced waters may be present at low to moderate concentrations in groundwater in various parts of the aquifer.

Pennsylvania↗

USGS1986

Surficial geology, structure, and thickness of selected geohydrologic units in the Columbia Plateau, Washington

A 2-1/2 year study of the Columbia Plateau in Washington was begun in March 1982 to define spatial and temporal variations in dissolved sodium in the Columbia River Basalt Group aquifers and to relate these variations to the groundwater system and its geologic framework. This report describes the geologic framework , including the vertical and areal extent of the major basalt units, interbeds, and overlying materials. Thickness and structure of the Grande Ronde, Wanapum, and Saddle Mountains Basalts, thickness of the interbeds between the Grande Ronde and Wanapum, and Wanapum and Saddle Mountains Basalts, and thickness of the overburden were mapped at a scale of 1:500,000. Information was compiled from 2,500 well records using chemical analyses of core or drill chips, geophysical logs, and driller 's logs, in decreasing order of reliability. Surficial geology and surficial expression of structural features were simplified from published maps to provide maps with this information at the 1:500,000 scale. This report is intended to serve as a base for evaluating the distribution of dissolved sodium in basalt aquifers and as a base for future water resource studies. (USGS)

Water-Resources Investigations Report↗

USGS2008

Relations of Water Quality to Agricultural Chemical Use and Environmental Setting at Various Scales - Results from Selected Studies of the National Water-Quality Assessment Program

In 1991, the U.S. Geological Survey (USGS) began studies of 51 major river basins and aquifers across the United States as part of the National Water-Quality Assessment (NAWQA) Program to provide scientifically sound information for managing the Nation's water resources. The major goals of the NAWQA Program are to assess the status and long-term trends of the Nation's surface- and ground-water quality and to understand the natural and human factors that affect it (Gilliom and others, 1995). In 2001, the NAWQA Program began a second decade of intensive water-quality assessments. The 42 study units for this second decade were selected to represent a wide range of important hydrologic environments and potential contaminant sources. These NAWQA studies continue to address the goals of the first decade of the assessments to determine how water-quality conditions are changing over time. In addition to local- and regional-scale studies, NAWQA began to analyze and synthesize water-quality status and trends at the principal aquifer and major river-basin scales. This fact sheet summarizes results from four NAWQA studies that relate water quality to agricultural chemical use and environmental setting at these various scales: * Comparison of ground-water quality in northern and southern High Plains agricultural settings (principal aquifer scale); * Distribution patterns of pesticides and degradates in rain (local scale); * Occurrence of pesticides in shallow ground water underlying four agricultural areas (local and regional scales); and * Trends in nutrients and sediment over time in the Missouri River and its tributaries (major river-basin scale).

Fact Sheet↗

USGS2016

Occurrence and distribution of arsenic and radon in water from private wells in the Rancocas aquifer, southern New Castle and northern Kent Counties, Delaware, 2015

Water samples were collected and analyzed for arsenic and radon from 36 private, mostly domestic wells that tap the Rancocas aquifer in southern New Castle and northern Kent Counties, Delaware, during the summer of 2015. Both arsenic and radon are from natural mineral sources, in particular glauconitic and other marine-derived sediments, which are important components of the geologic formations comprising the Rancocas aquifer. Routine testing of domestic wells is not required in Delaware; as a result, many homeowners are not aware of potential water-quality problems with these chemicals in their well water. Arsenic has previously been detected at levels of potential concern for human health in this aquifer in adjacent parts of Maryland where it is referred to as the Aquia aquifer. Arsenic and radon also have previously been detected in several Rancocas aquifer wells in Delaware. The Delaware Department of Natural Resources and Environmental Control intends to use the data from this project to better identify areas with potential for levels of concern for domestic well owners. This report includes chemical results and maps showing the distribution of sampled wells and concentrations of arsenic and radon. All data collected for this study also are available in the U.S. Geological Survey’s National Water Information System database. Arsenic was detected above the minimum reporting limit of 0.1 micrograms per liter (µg/L) in 34 of the 36 wells sampled with concentrations ranging from about 0.11 to 27 µg/L. In 15 of the samples, arsenic concentrations were at or above the U.S. Environmental Protection Agency (EPA) Maximum Contaminant Level (MCL) of 10 µg/L for public wells. Most of the higher concentrations are clustered along a band running from the southwest to northeast in the southern part of the study area. Radon, which is an inert gas derived from radium, was detected in all water samples with concentrations ranging from 85 to 1,870 picocuries per liter (pCi/L). Currently, the EPA has not set a MCL for radon in public water systems. There were no samples where radon was detected at a concentration exceeding the proposed alternative MCL of 4,000 pCi/L. Samples from 16 of 36 wells were above the lower proposed MCL of 300 pCi/L. Most of these samples were from wells greater than 200 feet deep located in a similar part of the aquifer as the higher concentrations of arsenic along an east-northeasterly line in the southern part of the study area.

Delaware↗

USGS2024

Temporally dense monitoring of pathogen occurrence at four drinking-water well sites – Insights and Implications

Yearlong, event based, microbiological and chemical sampling was conducted at four public water supply well sites spanning a range of geologic settings and well depths to look for correlation between precipitation events and microbial occurrence. Near-continuous monitoring using autosamplers occurred just before, during, and after 5–7 sampling events triggered by rainfall and/or snowmelt. Microbial genetic material was noted at all four locations during all but one sampling event, but was exceedingly variable in time, where one sample would have no detections and the next sample could be a relatively high concentration. The highest microbial sums (microbial concentrations summed over an event) were observed during months in which precipitation exceeded historical averages. Extended wet conditions through the spring thaw resulted in the highest percentage of microbial positive samples, though at relatively low concentrations. Sampling events that followed drier than normal periods showed longer lag times between the onset of precipitation and microbial occurrence, as well as lower microbial detection rates. Although a general lag time pattern was observed at each site, the largest offset in time was observed at the site with the greatest depth to water. The study's temporally dense representation of drinking water pathogen characterization suggests that single event or infrequent periodic sampling of a drinking water supply cannot provide a representative characterization of the probability that pathogens are present, which likely has ramifications for calculating health risk assessments.

Minnesota↗

USGS2002

Long-term tritium transport through field-scale compacted soil liner

A 13-year study of tritium transport through a field-scale earthen liner was conducted by the Illinois State Geological Survey to determine the long-term performance of compacted soil liners in limiting chemical transport. Two field-sampling procedures (pressure-vacuum lysimeter and core sampling) were used to determine the vertical tritium concentration profiles at different times and locations within the liner. Profiles determined by the two methods were similar and consistent. Analyses of the concentration profiles showed that the tritium concentration was relatively uniformly distributed horizontally at each sampling depth within the liner and thus there was no apparent preferential transport. A simple one-dimensional analytical solution to the advective-dispersive solute transport equation was used to model tritium transport through the liner. Modeling results showed that diffusion was the dominant contaminant transport mechanism. The measured tritium concentration profiles were accurately modeled with an effective diffusion coefficient of 6 ?? 10-4 mm2/s, which is in the middle of the range of values reported in the literature.

Journal of Geotechnical and Geoenvironmental Engin↗

USGS2012

MT3DMS: Model use, calibration, and validation

MT3DMS is a three-dimensional multi-species solute transport model for solving advection, dispersion, and chemical reactions of contaminants in saturated groundwater flow systems. MT3DMS interfaces directly with the U.S. Geological Survey finite-difference groundwater flow model MODFLOW for the flow solution and supports the hydrologic and discretization features of MODFLOW. MT3DMS contains multiple transport solution techniques in one code, which can often be important, including in model calibration. Since its first release in 1990 as MT3D for single-species mass transport modeling, MT3DMS has been widely used in research projects and practical field applications. This article provides a brief introduction to MT3DMS and presents recommendations about calibration and validation procedures for field applications of MT3DMS. The examples presented suggest the need to consider alternative processes as models are calibrated and suggest opportunities and difficulties associated with using groundwater age in transport model calibration.

Transactions of the ASABE↗

USGS1970

Hydrologic implications of solid-water disposal

The disposal of more than 1,400 million pounds of solid wastes in the United States each day is a major problem. This disposal in turn often leads to serious health, esthetic, and environmental problems. Among these is the pollution of vital ground-water resources. Of the six principal methods of solid-waste disposal in general use today, four methods-open dumps, sanitary landfill, incineration, and onsite disposal-carry an inherent potential for pollution of water resources. Seepage of rainwater through the wastes leaches undesirable constituents which reach the ground water in the area. This leachate is generally both biologically and chemically contaminated. The extent of the pollution from this leachate is largely dependent upon the geologic environment in which the solid wastes are deposited. Pollution potential is highest in permeable areas with a shallow water table where the wastes are in direct contact with the ground water. In a relatively impermeable area, the pollution is generally confined locally to the vicinity of the waste-disposal site. Site selection for disposal of solid wastes must be based on adequate water-resources information if pollutional potential is to be minimized. This will require regional as well as localized data on the water resources of the area. Only through such an approach can adequate protection be afforded to the environment in general and the water resources in particular.

Circular↗

USGS2010

Rocky Mountain snowpack physical and chemical data for selected sites, 2009

The Rocky Mountain Snowpack program established a network of snowpack-sampling sites in the Rocky Mountain region from New Mexico to Montana to monitor the chemical content of snow and to understand the effects of regional atmospheric deposition. The U.S. Geological Survey, in cooperation with the National Park Service; the U.S. Department of Agriculture Forest Service; the Colorado Department of Public Health and Environment; Teton County, Wyoming; and others, collected and analyzed snowpack samples annually for 48 or more sites in the Rocky Mountain region during 1993-2009. Sixty-three snowpack-sampling sites were sampled once each in 2009 and data are presented in this report. Data include acid-neutralization capacity, specific conductance, pH, hydrogen ion concentrations, dissolved concentrations of major constituents (calcium, magnesium, sodium, potassium, ammonium, chloride, sulfate, and nitrate), dissolved organic carbon concentrations, snow-water equivalent, snow depth, total mercury concentrations, and ionic charge balance. Quality-assurance data for field and laboratory blanks and field replicates for 2009 also are included.

Data Series↗

USGS2006

Data Delivery and Mapping Over the Web: National Water-Quality Assessment Data Warehouse

The U.S. Geological Survey began its National Water-Quality Assessment (NAWQA) Program in 1991, systematically collecting chemical, biological, and physical water-quality data from study units (basins) across the Nation. In 1999, the NAWQA Program developed a data warehouse to better facilitate national and regional analysis of data from 36 study units started in 1991 and 1994. Data from 15 study units started in 1997 were added to the warehouse in 2001. The warehouse currently contains and links the following data: -- Chemical concentrations in water, sediment, and aquatic-organism tissues and related quality-control data from the USGS National Water Information System (NWIS), -- Biological data for stream-habitat and ecological-community data on fish, algae, and benthic invertebrates, -- Site, well, and basin information associated with thousands of descriptive variables derived from spatial analysis, like land use, soil, and population density, and -- Daily streamflow and temperature information from NWIS for selected sampling sites.

Fact Sheet↗

USGS2002

Revised Protocols for Sampling Algal, Invertebrate, and Fish Communities as Part of the National Water-Quality Assessment Program

Algal, invertebrate, and fish communities are characterized as part of ecological studies in the U.S. Geological Survey.s National Water-Quality Assessment Program. Information from these ecological studies, together with chemical and physical data, provide an integrated assessment of water quality at local, regional, and national scales. Analysis and interpretation of water-quality data at these various geographic scales require accurate and consistent application of sampling protocols and sample-processing procedures. This report revises and unifies into a single document the algal, invertebrate, and fish community sampling protocols used in the National Water-Quality Assessment Program.

Open-File Report↗