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At least 973 records · Page 54Linked to original sources
USGS1976

Neutron activation analysis in hydrology

Neutron activation analysis in hydrogeochemical and related investigations is increasingly practical because of developments in radiation detectors and computerized data processing. While neutron activation is the most widely used kind of activation analysis other kinds (for example, charged particle activation) are available for special applications. Neutron activation analysis is promising because approximately 70 percent of the elements in the periodic table are detected with satisfactory sensitivity, contamination from reagents is eliminated, simultaneous determination of more than 20 elements is often possible, technique is versatile, is applicable to small samples and is non-destructive in the instrumental form. Developments in theU.S. Geological Survey include a special sampling technique for water; a comprehensive technique using carriers precipitated with sulfide to concentrate desired trace elements; a determination of mercury, silver, and gold; determination of aluminum, vanadium and nine other elements; determinations of two groups of rare earth elements; and adaptations of the analytical methods to sediment and biota.

Open-File Report↗
USGS2020

Water resources in the Cheyenne and Arapaho Tribal jurisdictional area, west-central Oklahoma, with an analysis of data gaps through 2015

This report provides an overview of existing hydrologic information describing the quality, quantity, and extent of the major surface-water and groundwater resources in the Cheyenne and Arapaho Tribal jurisdictional area, west-central Oklahoma. Hydrologic information is provided for five major river systems (Cimarron River, North Canadian River, Canadian River, Washita River, and North Fork Red River), two reservoirs (Foss Reservoir and Canton Lake), and eight aquifers consisting of the alluvial aquifers associated with each of the five major river systems and three major bedrock aquifers (Ogallala aquifer, Elk City aquifer, and Rush Springs aquifer). Types of information provided about rivers and reservoirs for the Cheyenne and Arapaho Tribal jurisdictional area include diversion sites and amounts of water allocated and diverted for permitted uses in 2015; treated wastewater discharge sites and amounts discharged in 2015; and characteristics describing water-quality field properties, major ions, nutrients, and selected trace elements. Major ions, nutrients, and selected trace elements are compared to secondary maximum contaminant levels and maximum contaminant levels for finished drinking water. Additionally, statistics are provided describing daily, monthly, and annual streamflow characteristics at 12 U.S. Geological Survey streamgages. Streamflow statistics include the magnitudes and frequencies of floods, base-flow characteristics, and long-term streamflow trends. Types of information provided about the aquifers include amounts of water allocated and pumped for permitted uses in 2015; characteristics of groundwater describing water-quality field properties, major ions, nitrate (measured as nitrogen), and selected trace elements with comparisons to secondary maximum contaminant levels and maximum contaminant levels for finished drinking water; groundwater levels and long-term changes in water levels; and ranges of hydraulic conductivity, aquifer recharge, specific yield, transmissivity, and well yields from reports and groundwater-flow models. Surface water is used primarily for irrigation and mining and other nonconsumptive uses in the Cheyenne and Arapaho Tribal jurisdictional area, except from the Washita and North Fork Red Rivers, where water is treated for use as a public-water supply. Large concentrations of dissolved solids are the primary limiting factor affecting the use of surface water. Median concentrations of dissolved solids in surface water range from less than 1,000 milligrams per liter (mg/L) in samples from the North Canadian River to greater than 9,000 mg/L in samples from the Cimarron River. Large dissolved solids concentrations are correlated with hard water. Median hardness as calcium carbonate concentrations in surface water ranges from 427 mg/L in samples from Canton Lake to 1,000 mg/L in samples from the Washita River. In 2015, groundwater was used at more than twice the rate of surface water in the Cheyenne and Arapaho Tribal jurisdictional area. Although the alluvial aquifers are considered reliably good sources of water in the Cheyenne and Arapaho Tribal jurisdictional area, concentrations of nitrate (measured as nitrogen) exceed the maximum contaminant level of 10 mg/L established by the U.S. Environmental Protection Agency for finished drinking water in parts of all of the alluvial aquifers. Water from the three major bedrock aquifers is used for irrigation, mining, public-water supply, and other uses; however, large concentrations of dissolved solids, nitrate (measured as nitrogen), and naturally occurring trace elements such as arsenic and uranium may limit the use of groundwater as a source of public-water supply in some areas. As of 2015, the depletion of groundwater from the major aquifers in west-central Oklahoma is a minor concern to the Oklahoma Water Resources Board. Groundwater levels and other hydrologic information show that recharge rates exceed the rates of water pumped from aquifers, except in areas that may be affected locally by groundwater depletions.

Oklahoma↗
USGS2003

Irrigation-induced contamination of water, sediment, and biota in the western United States-synthesis of data from the National Irrigation Water Quality Program

In October 1985 the U.S. Department of the Interior (DOI), through the National Irrigation Water Quality Program (NIWQP), began a series of field investigations at 26 areas in the Western United States to determine whether irrigation drainage has had harmful effects on fish, wildlife, and humans or has reduced beneficial uses of water. In 1992 NIWQP initiated the Data Synthesis Project to evaluate data collected during the field investigations. Geologic, climatologic, and hydrologic data were evaluated and water, sediment, and biota from the 26 areas were analyzed to identify commonalities and dominant factors that result in irrigation-induced contamination of water and biota. Data collected for the 26 area investigations have been compiled and merged into a common data base. The structure of the data base is designed to enable assessment of relations between contaminant concentrations in water, sediment, and biota. The data base is available to the scientific community through the World Wide Web at URL http://www.usbr.gov/niwqp. Analysis of the data base for the Data Synthesis included use of summary statistics, factor analysis, and logistic regression. A Geographic Information System was used to store and analyze spatially oriented digital data such as land use, geology and evaporation rates. In the U.S. Department of the Interior (DOI) study areas, samples of water, bottom sediment, and biota were collected for trace-element and pesticide analysis. Contaminants most commonly associated with irrigation drainage were identified by comparing concentrations in water with established criteria. For surface water, the criteria used were typically chronic criteria for the protection of freshwater aquatic life. Because ground water can discharge to the surface where wildlife can be exposed to it, the criteria used for ground water were both the maximum contaminant levels (MCL's) for drinking water and the chronic criteria for the protection of freshwater aquatic life. Data collected by the NIWQP studies indicated that, in surface water, filtered and unfiltered samples had nearly the same concentrations of arsenic, boron, molybdenum, and selenium for concentrations greater than about 10 micrograms per liter. Therefore, in this concentration range, filtered concentrations can be directly compared to biological-effect levels developed for unfiltered samples. In the range of 1 to 10 micrograms per liter there may be a tendency for unfiltered arsenic concentrations to be greater than filtered concentrations. For selenium, however, the data suggest differences from equality in that range result from analytical imprecision and not a general tendency for unfiltered concentrations to be greater than filtered concentrations. This relation may not be true in lentic, nutrient-rich waters because in such settings algae can bioaccumulate large amounts of selenium and other trace elements. Selenium was the trace element in surface water that most commonly exceeded chronic criteria for the protection of freshwater aquatic life; more than 40 percent of the selenium concentrations in surface-water samples exceeded the U.S. Environmental Protection Agency (USEPA) aquatic-life chronic criterion (5 micrograms per liter). In 12 of the 26 areas at least 25 percent of the surface water-samples had selenium concentrations that either equaled or exceeded the chronic criterion (5 micrograms per liter). More than 28 percent of boron concentrations and almost 17 percent of the molybdenum concentrations exceeded the aquatic life criteria established by the State of California (550 and 19 micrograms per liter, respectively). In ground water, more than 22 percent of the arsenic concentrations and more than 35 percent of the selenium concentrations exceeded the MCL (10 and 50 micrograms per liter, respectively). Few samples of uranium in surface water exceeded a criterion for the protection of aquatic life (300 micrograms per liter), but 44 percent

Professional Paper↗
USGS2005

Yellowstone grizzly bear investigations: Annual report of the Interagency Grizzly Bear Study Team, 2004

The contents of this Annual Report summarize results of monitoring and research from the 2004 field season. The report also contains a summary of nuisance grizzly bear ( Ursus arctos horribilis ) management actions. The study team continues to work on issues associated with counts of unduplicated females with cubs-of-the-year (COY). These counts are used to establish a minimum population size, which is then used to establish mortality thresholds for the Recovery Plan (U.S. Fish and Wildlife Service [USFWS] 1993). A computer program that defines the rule set used by Knight et al. (1995) to differentiate unique family groups was completed in spring 2005. We will use an improved version of this model to verify the accuracy of the rules using known bears and their telemetry locations in test runs. We hope to have this work complete by the end of 2005. The grizzly bear recovery plan (USFWS 1993) established mortality quotas at 4% of the minimum population estimate derived from female with COY data and no more than 30% of the 4% (1.2%) could be female bears. Simulation modeling (Harris 1984) established sustainable mortality at around 6% of the population. We used the latest information on reproduction and survival to estimate population trajectory in the same simulation model originally used by Harris. A Wildlife Monograph has been accepted for publication and should be available by summer 2005. Our project addressing the potential application of stable isotopes and trace elements to quantify consumption rates of whitebark pine ( Pinus albicaulis ) and cutthroat trout ( Oncorhynchus clarki ) by grizzly bears was completed. Our manuscript on consumption rates of whitebark pine has been published (Canadian Journal of Zoology 81:763-770). The manuscript on fish consumption rates was also accepted and is published in the Canadian Journal of Zoology 82:493-501. Both can be found on the Interagency Grizzly Bear Study Team (IGBST) website http://www.nrmsc.usgs.gov/research/igbst-home.htm. We began a new study in Grand Teton National Park evaluating habitat use both temporally and spatially between grizzly and black ( Ursus americanus ) bears. We will employ a new form of Global Positioning System (GPS) technology that incorporates a spread spectrum communication system. Spread spectrum allows for transfer of stored GPS locations from the collar to a remote receiving station. Results of our first yea r’s field season are summarized in this report. Whitebark pine (WBP) has been identified as one of the import ant fall foods of the Yellowstone grizzly bear. Previous efforts to map the distribution of WBP were for the Cumulative Effects Model. Consequently the only coverage of WBP distribution was for the grizzly bear Recovery Zone. We were successful in getting financial support through the U.S. Geological Survey Land Remote Sensing Program and Interdisciplinary Science Support Activities Project to create an ecosystem-wide map of the distribution of WBP. The results of that project are reported in Appendix A. The study team annually estimates WBP cone production on a series of transects. That information is reported annually in our reports. Concern over the long-term health of WBP prompted us to investigate the usefulness of cone counts as an indirect index of WBP health. Results of this analysis (Appendix B) indicated that cone production is too variable to serve this purpose. Consequently, we partnered with several 2 other agencies and embarked on a program to develop a long-term monitoring program directed specifically at WBP health in the Greater Yellowstone Ecosystem (GYE). Our team (Greater Yellowstone Whitebark Pine Monitoring Working Group) was successful in obtaining funds to develop and implement a WBP health monitoring program. Results of our first years work are presented in Appendix C. We also successfully competed for funds in 2005 and will continue to collect information on WBP health. Army cutworm moths ( Euxoa auxiliaris ) are also a very important food for a segment of the GYE grizzly bear population. Hillary Robison, graduate student at University of Nevada, Reno, is nearing completion of her program. In this report, we post her annual work summary, and abstracts of her most recently submitted publications. These include one on the levels of pesticides in cutworm moths and their potential affect on grizzly bears (Appendix D), a spatial analysis to identify army cutworm moth habitat (Appendix E), and the results of a preliminary analysis of pollen grains on the mouth parts of moths (Appendix F) to help identify which plant species are commonly fed upon. Other study team members have also been working on various aspects of grizzly bear science. Study team member Kerry Gunther hosted a workshop on habituated grizzly bears in North America. A copy of the abstract of that report can be found in Appendix G. Additionally, Kerry Gunther and Doug Smith, wolf researcher in Yellowstone National Park (YNP), reported on the interactions between gray wolves ( Canis lupus ) and female grizzly bears with young. They report that of 15 interactions between these 2 carnivores, 8 involve d females with COY. They observed 2 incidents where cubs were killed by wolves at ungulate carcasses (Appendix H). The annual reports of the IGBST summarize annual data collection. Because additional information can be obtained after publication, data summaries are subject to change. For that reason, data analyses and summaries presented in this report supersede all previously published data. The study area and sampling techniques are reported by Blanchard (1985), Mattson et al. (1991 a ), and Haroldson et al. (1998).

Idaho, Montana, Wyoming↗
USGS2011

Lagrangian sampling of wastewater treatment plant effluent in Boulder Creek, Colorado, and Fourmile Creek, Iowa, during the summer of 2003 and spring of 2005— Hydrological and water-quality data

This report presents methods and data for a Lagrangian sampling investigation into chemical loading and in-stream attenuation of inorganic and organic contaminants in two wastewater treatment-plant effluent-dominated streams: Boulder Creek, Colorado, and Fourmile Creek, Iowa. Water-quality sampling was timed to coincide with low-flow conditions when dilution of the wastewater treatment-plant effluent by stream water was at a minimum. Sample-collection times corresponded to estimated travel times (based on tracer tests) to allow the same "parcel" of water to reach downstream sampling locations. The water-quality data are linked directly to stream discharge using flow- and depth-integrated composite sampling protocols. A range of chemical analyses was made for nutrients, carbon, major elements, trace elements, biological components, acidic and neutral organic wastewater compounds, antibiotic compounds, pharmaceutical compounds, steroid and steroidal-hormone compounds, and pesticide compounds. Physical measurements were made for field conditions, stream discharge, and time-of-travel studies. Two Lagrangian water samplings were conducted in each stream, one in the summer of 2003 and the other in the spring of 2005. Water samples were collected from five sites in Boulder Creek: upstream from the wastewater treatment plant, the treatment-plant effluent, and three downstream sites. Fourmile Creek had seven sampling sites: upstream from the wastewater treatment plant, the treatment-plant effluent, four downstream sites, and a tributary. At each site, stream discharge was measured, and equal width-integrated composite water samples were collected and split for subsequent chemical, physical, and biological analyses. During the summer of 2003 sampling, Boulder Creek downstream from the wastewater treatment plant consisted of 36 percent effluent, and Fourmile Creek downstream from the respective wastewater treatment plant was 81 percent effluent. During the spring of 2005 samplings, Boulder Creek downstream from the wastewater treatment plant was 40 percent effluent, and Fourmile Creek downstream from that wastewater treatment plant was 28 percent effluent. At each site, 300 individual constituents were determined to characterize the water. Most of the inorganic constituents were detected in all of the stream and treatment-plant effluent samples, whereas detection of synthetic organic compounds was more limited and contaminants typically occurred only in wastewater treatment-plant effluents and at downstream sites. Concentrations ranged from nanograms per liter to milligrams per liter.

Colorado, Iowa↗
USGS2003

Trends in chemical concentration in sediment cores from three lakes in New Jersey and one lake on Long Island, New York

Sediment cores were extracted from three lakes in northeastern New Jersey and one lake on western Long Island, New York, as part of the U.S. Geological Survey National Water-Quality Assessment Program. Sediment layers were dated by use of cesium-137 (137Cs), copper, lead, or dichlorodiphenyl-trichloroethane (DDT) profiles. Sediment layers were analyzed for seven selected trace elements, including arsenic, cadmium, chromium, lead, mercury, nickel, and zinc, and five hydrophobic organochlorine compounds, including chlordane, dieldrin, total DDT, total polychlorinated biphenyls (PCBs), and total polycyclic aromatic hydrocarbons (PAHs). All seven trace elements were detected throughout the cores from all four lakes. Concentrations of all elements, except arsenic, were elevated in the three cores from lakes within urbanized watersheds (Packanack Lake, Orange Reservoir, and Newbridge Pond) relative to the concentrations in the lake core collected below the largely forested, reference watershed (Clyde Potts Reservoir). Results of trend analyses indicate that concentrations of all trace elements, with the exception of arsenic and lead, were relatively constant throughout the core from the minimally urbanized Clyde Potts Reservoir. In urban lakes, significant upward trends in concentrations from deeper to shallower sediments were observed either to peak concentrations or throughout the core for all elements, with the exception of chromium at all lakes and arsenic and nickel at Orange Reservoir. This finding indicates that changes in population and land use in the urbanized watersheds over the period of sedimentary record have contributed to upward trends in trace-element concentrations. Although downward trends in concentrations were observed for some trace elements in the years after their concentrations peaked, concentrations of all trace elements in urban lake cores were higher in the most recently deposited sediments than at the base of each respective core. Lead concentrations over time were highly correlated with the population in the vicinity of the lake until the concentration peak in sediment deposited in the mid-1970’s. Concentrations of lead in lake sediment appear to be closely related to the use of leaded gasoline because lead concentrations generally decreased after the use of leaded gasoline was phased-out in the mid-1970’s. Zinc concentrations were highly correlated with population over the entire length of the core. In general, zinc concentrations increased in the three urbanized watersheds, probably in response to increasing population and vehicular use. This trend was not evident at Clyde Potts Reservoir, however, where vehicular traffic in the watershed is minimal. Detectable concentrations of chlordane, total DDT, and total PCBs were present in cores from all lakes; however, dieldrin was detected only in the Newbridge Pond and Packanack Lake cores. Concentrations generally were higher in cores from the urbanized Newbridge Pond and Orange Reservoir watersheds than in those from the minimally urbanized Clyde Potts Reservoir watershed. With the exception of chlordane in the Clyde Potts and Orange Reservoir cores, concentrations of the four organochlorine compounds had significant downward trends from peak concentrations to recently deposited sediment or non-significant trends throughout the core. On the basis of these findings and as a result of regulatory actions prohibiting the production and use of these compounds, downward trends in sedimentary concentrations are expected to continue; however, the persistence of these compounds indicates that a substantial amount of time may be required to purge them from the watersheds. Concentrations of PAHs in sediment generally increased with population growth and urbanization, probably as a result of increased fossil-fuel combustion (gasoline and home-heating fuels and other uses (roads and parking lots paved with asphalt) associated with increased urban development and vehicular traffic. This finding is supported by low concentrations of PAHs in Packanack Lake sediments in the 1930’s, before the watershed was urbanized and when automobiles were comparatively rare. As vehicular use and urbanization increase in these watersheds, the general increase of PAH concentrations in lake sediments can be expected to continue. Data from this study indicate that changes in population, land use, and chemical use in the urbanized watersheds over the period of sedimentary record have contributed to upward trends in concentrations of trace elements and hydrophobic organic compounds. Although downward trends were observed for some constituents in the years after their concentrations peaked, concentrations of most constituents in urban lake cores were higher in the most recently deposited sediments than at the base of each respective core and in the reference lake cores. Similar trends in concentrations of these constituents have been observed in sediment cores from other urban lakes across the United States.

New Jersey, New York↗
USGS1987

Surface water-quality characteristics in the upper North Fork Gunnison River basin, Colorado

Analyses of water quality data collected during 1982 and 1983 in the upper North Fork Gunnison River basin indicate that dissolved-solids concentrations are relatively small, with a mean value near 97 milligrams per liter. Most major dissolved constituents also had small measured concentrations throughout the study area. Trace-element concentrations generally were small; however, total-iron concentration generally was large in the area with a mean concentration of about 8,250 micrograms per liter. The cause of this larger iron concentration probably is related to the local geology. Paonia Reservoir, located on Muddy Creek, greatly reduced suspended-sediment and trace-element concentrations. The reservoir had only a slight effect on major dissolved-constituent concentrations. Analyses of alkalinity, sulfate, and dissolved-solids concentrations indicated that little, if any, changes in water quality occur as a result of coal mining; however, more data are needed to make more definite conclusions. Sulfate concentrations increased slightly downstream through the mined area; however, with the small concentrations measured and limited quantity of data, the source of the increased sulfate could not be determined. (USGS)

Water-Resources Investigations Report↗
USGS2009

Water- and Bed-Sediment Quality of Seguchie Creek and Selected Wetlands Tributary to Mille Lacs Lake in Crow Wing County, Minnesota, October 2003 to October 2006

Mille Lacs Lake and its tributaries, located in east-central Minnesota, are important resources to the public. In addition, many wetlands and lakes that feed Mille Lacs Lake are of high resource quality and vulnerable to degradation. Construction of a new four-lane expansion of U.S. Highway 169 has been planned along the western part of the drainage area of Mille Lacs Lake in Crow Wing County. Concerns exist that the proposed highway could affect the resource quality of surface waters tributary to Mille Lacs Lake. Baseline water- and bed-sediment quality characteristics of surface waters tributary to Mille Lacs Lake were needed prior to the proposed highway construction. The U.S. Geological Survey, in cooperation with the Minnesota Department of Transportation, characterized the water- and bed-sediment quality at selected locations that the proposed route intersects from October 2003 to October 2006. Locations included Seguchie Creek upstream and downstream from the proposed route and three wetlands draining to Mille Lacs Lake. The mean streamflow of Seguchie Creek increased between the two sites: flow at the downstream streamflow-gaging station of 0.22 cubic meter per second was 5.6 percent greater than the mean streamflow at the upstream streamflow-gaging station of 0.21 cubic meter per second. Because of the large amount of storage immediately upstream from both gaging stations, increases in flow were gradual even during intense precipitation. The ranges of most constituent concentrations in water were nearly identical between the two sampling sites on Seguchie Creek. No concentrations exceeded applicable water-quality standards set by the State of Minnesota. Dissolved-oxygen concentrations at the downstream gaging station were less than the daily minimum standard of 4.0 milligrams per liter for 6 of 26 measurements. Constituent loads in Seguchie Creek were greater at the downstream site than the upstream site for all measured, including dissolved chloride (1.7 percent), ammonia plus organic nitrogen (13 percent), total phosphorus (62 percent), and suspended sediment (11 percent) during the study. All constituents had seasonal peaks in spring and fall. The large loads during the fall resulted from unusually large precipitation and streamflow patterns. This caused the two greatest streamflow peaks at both sites to occur during October (2004 and 2005). In Seguchie Creek, bed-sediment concentrations of five metals and trace elements (arsenic, cadmium, chromium, lead, and zinc) exceeded the Interim Sediment Quality Guidelines (ISQG) set by the Canadian Council of Ministers of the Environment. Bed-sediment samples from the upstream site had more exceedances of ISQGs for metals and trace elements than did samples from the downstream site (seven and two exceedances, respectively). Bed-sediment samples from the downstream site had more exceedances of ISQGs (20 exceedances) for semivolatile organic compounds than did samples from the upstream site (8 exceedances), indicating different sources for organic compounds than for metals and trace elements. Concentrations of 11 semivolatile organic compounds exceeded ISQGs: ancenaphthene, acenaphthylene, anthracene, benzo[a]anthracene, benzo[a]pyrene, chrysene, fluoranthene, fluorene, naphthalene, phenanthrene, and pyrene. In bed-sediment samples collected from three wetlands, concentrations of all six metals exceeded ISQGs: arsenic, cadmium, chromium, copper, lead, and zinc. Concentrations of three semivolatile organic compounds exceeded ISQGs: flouranthene, phenanthrene, and pyrene. Results indicate that areas appearing relatively undisturbed and of high resource value can have degraded quality from previous unknown land use.

Scientific Investigations Report↗
USGS2010

Arsenic-related water quality with depth and water quality of well-head samples from production wells, Oklahoma, 2008

The U.S. Geological Survey well profiler was used to describe arsenic-related water quality with well depth and identify zones yielding water with high arsenic concentrations in two production wells in central and western Oklahoma that yield water from the Permian-aged Garber-Wellington and Rush Springs aquifers, respectively. In addition, well-head samples were collected from 12 production wells yielding water with historically large concentrations of arsenic (greater than 10 micrograms per liter) from the Garber-Wellington aquifer, Rush Springs aquifer, and two minor aquifers: the Arbuckle-Timbered Hills aquifer in southern Oklahoma and a Permian-aged undefined aquifer in north-central Oklahoma. Three depth-dependent samples from a production well in the Rush Springs aquifer had similar water-quality characteristics to the well-head sample and did not show any substantial changes with depth. However, slightly larger arsenic concentrations in the two deepest depth-dependent samples indicate the zones yielding noncompliant arsenic concentrations are below the shallowest sampled depth. Five depth-dependent samples from a production well in the Garber-Wellington aquifer showed increases in arsenic concentrations with depth. Well-bore travel-time information and water-quality data from depth-dependent and well-head samples showed that most arsenic contaminated water (about 63 percent) was entering the borehole from perforations adjacent to or below the shroud that overlaid the pump. Arsenic concentrations ranged from 10.4 to 124 micrograms per liter in 11 of the 12 production wells sampled at the well head, exceeding the maximum contaminant level of 10 micrograms per liter for drinking water. pH values of the 12 well-head samples ranged from 6.9 to 9. Seven production wells in the Garber-Wellington aquifer had the largest arsenic concentrations ranging from 18.5 to 124 micrograms per liter. Large arsenic concentrations (10.4-18.5) and near neutral to slightly alkaline pH values (6.9-7.4) were detected in samples from one well in the Garber-Wellington aquifer, three production wells in the Rush Springs aquifer, and one well in an undefined Permian-aged aquifer. All well-head samples were oxic and arsenate was the only species of arsenic in water from 10 of the 12 production wells sampled. Arsenite was measured above the laboratory reporting level in water from a production well in the Garber-Wellington aquifer and was the only arsenic species measured in water from the Arbuckle-Timbered Hills aquifer. Fluoride and uranium were the only trace elements, other than arsenic, that exceeded the maximum contaminant level for drinking water in well-head samples collected for the study. Uranium concentrations in four production wells in the Garber-Wellington aquifer ranged from 30.2 to 99 micrograms per liter exceeding the maximum contaminant level of 30 micrograms per liter for drinking water. Water from these four wells also had the largest arsenic concentrations measured in the study ranging from 30 to 124 micrograms

Scientific Investigations Report↗
USGS1995

Quality of surface water and ground water in the proposed artificial-recharge project area, Rillito Creek basin, Tucson, Arizona, 1994

Controlled artificial recharge of surface runoff is being considered as a water-management technique to address the problem of ground-water overdraft. The planned use of recharge facilities in urban areas has caused concern about the quality of urban runoff to be recharged and the potential for ground-water contamination. The proposed recharge facility in Rillito Creek will utilize runoff entering a 1-mile reach of the Rillito Creek between Craycroft Road and Swan Road for infiltration and recharge purposes within the channel and excavated overbank areas. Physical and chemical data were collected from two surface-water and two ground-water sites in the study area in 1994. Analyses of surface-water samples were done to determine the occurrence and concentration of potential contaminants and to determine changes in quality since samples were collected during 1987-93. Analyses of ground-water samples were done to determine the variability of ground-water quality at the monitoring wells throughout the year and to determine changes in quality since samples were collected in 1989 and 1993. Surface-water samples were collected from Tanque Verde Creek at Sabino Canyon Road (streamflow-gaging station Tanque Verde Creek at Tucson, 09484500) and from Alamo Wash at Fort Lowell Road in September and May 1994, respectively. Ground-water samples were collected from monitoring wells (D- 13-14)26cbb2 and (D-13-14)26dcb2 in January, May, July, and October 1994. In surface water, calcium was the dominant cation, and bicarbonate was the dominant anion. In ground water, calcium and sodium were the dominant cations and bicarbonate was the dominant anion. Surface water in the area is soft, and ground water is moderately hard to hard. In surface water and ground water, nitrogen was found predominantly as nitrate. Concentrations of manganese in ground-water samples ranged from 60 to 230 micrograms per liter and exceeded the U.S. Environmental Protection Agency secondary maximum contaminant level for drinking water of 50 micrograms per liter. None of the constituents in surface-water and ground-water samples exceeded the U.S. Environmental Protection Agency primary maximum contaminant levels for drinking water or State of Arizona aquifer water-quality standards. Concentrations of major ions, nutrients, and trace elements in water from the monitoring wells did not vary significantly throughout the year and were not significantly different from concentrations in samples collected in March 1989 and January and September 1993. Priority pollutants were not found in surface-water samples or ground-water samples, and organochlorine pesticides were not found in ground-water samples. Dieldrin and biphenyl polychlor were the only pesticides found in surface water and were at the minimum reporting levels in one sample from Alamo Wash.

Water-Resources Investigations Report↗
USGS1995

Coal geology of the Paleocene-Eocene Calvert Bluff Formation (Wilcox Group) and the Eocene Manning Formation (Jackson Group) in east-central Texas: Field trip guidebook for the Society for Organic Petrology, Twelfth Annual Meeting, The Woodlands, Texas, August 30, 1995

The Jackson and Wilcox Groups of eastern Texas (fig. 1) are the major lignite producing intervals in the Gulf Region. Within these groups, the major lignite-producing formations are the Paleocene-Eocene Calvert Bluff Formation (Wilcox) and the Eocene Manning Formation (Jackson). According to the Keystone Coal Industry Manual (Maclean Hunter Publishing Company, 1994), the Gulf Coast basin produces about 57 million short tons of lignite annually. The state of Texas ranks number 6 in coal production in the United States. Most of the lignite is used for electric power generation in mine-mouth power plant facilities. In recent years, particular interest has been given to lignite quality and the distribution and concentration of about a dozen trace elements that have been identified as potential hazardous air pollutants (HAPs) by the 1990 Clean Air Act Amendments. As pointed out by Oman and Finkelman (1994), Gulf Coast lignite deposits have elevated concentrations of many of the HAPs elements (Be, Cd, Co, Cr, Hg, Mn, Se, U) on a as-received gm/mmBtu basis when compared to other United States coal deposits used for fuel in thermo-electric power plants. Although regulations have not yet been established for acceptable emissions of the HAPs elements during coal burning, considerable research effort has been given to the characterization of these elements in coal feed stocks. The general purpose of the present field trip and of the accompanying collection of papers is to investigate how various aspects of east Texas lignite geology might collectively influence the quality of the lignite fuel. We hope that this collection of papers will help future researchers understand the complex, multifaceted interrelations of coal geology, petrology, palynology and coal quality, and that this introduction to the geology of the lignite deposits of east Texas might serve as a stimulus for new ideas to be applied to other coal basins in the U.S. and abroad.

Texas↗
USGS2006

Geochemical Characterization of Mine Waste, Mine Drainage, and Stream Sediments at the Pike Hill Copper Mine Superfund Site, Orange County, Vermont

The Pike Hill Copper Mine Superfund Site in the Vermont copper belt consists of the abandoned Smith, Eureka, and Union mines, all of which exploited Besshi-type massive sulfide deposits. The site was listed on the U.S. Environmental Protection Agency (USEPA) National Priorities List in 2004 due to aquatic ecosystem impacts. This study was intended to be a precursor to a formal remedial investigation by the USEPA, and it focused on the characterization of mine waste, mine drainage, and stream sediments. A related study investigated the effects of the mine drainage on downstream surface waters. The potential for mine waste and drainage to have an adverse impact on aquatic ecosystems, on drinking- water supplies, and to human health was assessed on the basis of mineralogy, chemical concentrations, acid generation, and potential for metals to be leached from mine waste and soils. The results were compared to those from analyses of other Vermont copper belt Superfund sites, the Elizabeth Mine and Ely Copper Mine, to evaluate if the waste material at the Pike Hill Copper Mine was sufficiently similar to that of the other mine sites that USEPA can streamline the evaluation of remediation technologies. Mine-waste samples consisted of oxidized and unoxidized sulfidic ore and waste rock, and flotation-mill tailings. These samples contained as much as 16 weight percent sulfides that included chalcopyrite, pyrite, pyrrhotite, and sphalerite. During oxidation, sulfides weather and may release potentially toxic trace elements and may produce acid. In addition, soluble efflorescent sulfate salts were identified at the mines; during rain events, the dissolution of these salts contributes acid and metals to receiving waters. Mine waste contained concentrations of cadmium, copper, and iron that exceeded USEPA Preliminary Remediation Goals. The concentrations of selenium in mine waste were higher than the average composition of eastern United States soils. Most mine waste was potentially acid generating because of paste-pH values of less than 4 and negative net-neutralization potentials (NNP). The processed flotation-mill tailings, however, had a near neutral paste pH, positive NNP, and a few weight percent calcite. Leachate tests indicated that elements and compounds such as Al, Cd, Cu, Fe, Mn, Se, SO4, and Zn were leached from mine waste in concentrations that exceeded aquatic ecosystem and drinking-water standards. Mine waste from the Pike Hill mines was chemically and mineralogically similar to that from the Elizabeth and Ely mines. In addition, metals were leached and acid was produced from mine waste from the Pike Hill mines in comparable concentrations to those from the Elizabeth and Ely mines, although the host rock of the Pike Hill deposits contains significant amounts of carbonate minerals and, thus, a greater acid-neutralizing capacity when compared to the host rocks of the Elizabeth and Ely deposits. Water samples collected from unimpacted parts of the Waits River watershed generally contained lower amounts of metals compared to water samples from mine drainage, were alkaline, and had a neutral pH, which was likely because of calcareous bedrock. Seeps and mine pools at the mine site had acidic to neutral pH, ranged from oxic to anoxic, and generally contained concentrations of metals, for example, aluminum, cadmium, copper, iron, and zinc, that exceeded aquatic toxicity standards or drinking-water standards, or both. Surface waters directly downstream of the Eureka and Union mines were acidic, as indicated by pH values from 3.1 to 4.2, and contained high concentrations of some elements including as much as 11,400 micrograms per liter (?g/L) Al, as much as 22.9 ?g/L Cd, as much as 6,790 ?g/L Cu, as much as 23,300 ?g/L Fe, as much as 1,400 ?g/L Mn, and as much as 3,570 ?g/L Zn. The concentrations of these elements exceeded water-quality guidelines. Generally, in surface waters, the pH increased and the concentrations of these elemen

Scientific Investigations Report↗
USGS2009

Transport and sources of suspended sediment in the Mill Creek Watershed, Johnson County, Northeast Kansas, 2006-07

The U.S. Geological Survey, in cooperation with the Johnson County Stormwater Management Program, evaluated suspended-sediment transport and sources in the urbanizing, 57.4 mi2 Mill Creek watershed from February 2006 through June 2007. Sediment transport and sources were assessed spatially by continuous monitoring of streamflow and turbidity as well as sampling of suspended sediment at nine sites in the watershed. Within Mill Creek subwatersheds (2.8-16.9 mi2), sediment loads at sites downstream from increased construction activity were substantially larger (per unit area) than those at sites downstream from mature urban areas or less-developed watersheds. Sediment transport downstream from construction sites primarily was limited by transport capacity (streamflow), whereas availability of sediment supplies primarily influenced transport downstream from mature urban areas. Downstream sampling sites typically had smaller sediment loads (per unit area) than headwater sites, likely because of sediment deposition in larger, less sloping stream channels. Among similarly sized storms, those with increased precipitation intensity transported more sediment at eight of the nine monitoring sites. Storms following periods of increased sediment loading transported less sediment at two of the nine monitoring sites. In addition to monitoring performed in the Mill Creek watershed, sediment loads were computed for the four other largest watersheds (48.6-65.7 mi2) in Johnson County (Blue River, Cedar, Indian, and Kill Creeks) during the study period. In contrast with results from smaller watersheds in Mill Creek, sediment load (per unit area) from the most urbanized watershed in Johnson County (Indian Creek) was more than double that of other large watersheds. Potential sources of this sediment include legacy sediment from earlier urban construction, accelerated stream-channel erosion, or erosion from specific construction sites, such as stream-channel disturbance during bridge renovation. The implication of this finding is that sediment yields from larger watersheds may remain elevated after the majority of urban development is complete. Surface soil, channel-bank, suspended-sediment, and streambed-sediment samples were analyzed for grain size, nutrients, trace elements, and radionuclides in the Mill Creek watershed to characterize suspended sediment between surface or channel-bank sources. Although concentrations and activities of cobalt, nitrogen, selenium, total organic carbon, cesium-137, and excess lead-210 had significant differences between surface and channel-bank samples, biases resulting from urban construction, additional sorption of constituents during sediment transport, and inability to accurately represent erosion from rills and gullies precluded accurate characterization of suspended-sediment source.

Kansas↗
USGS2013

Lead isotope determinations from sulfide mineral occurrences--Russian Far East

The lead isotope database for sulfide deposits and occurrences in the Russian Far East was funded by the Mineral Resources Program, U.S. Geological Survey (USGS) in conjunction with the collaborative studies of mineral resources by the Russian Academy of Sciences and the U. S. Geological Survey (Nokleberg and others, 1996). Comparisons of these data with similar lead isotope data from Alaska published in Church, Delevaux, and others (1987) and Gaccetta and Church (1989) provide a basis for the following three-fold project objectives: 1. To utilize lead isotope signatures, in conjunction with regional mapping, to assess the relative ages and to categorize the types of mineral deposits studied, 2. To relate the lead isotope and trace-element geochemical signatures of specific deposits and occurrences to ore-forming processes, and 3. To use the lead isotope data to correlate lithotectonic terranes within the northern Cordillera (Alaska, Yukon Territories and British Columbia in Canada, and the western Cordillera of the United States). The report by Church, Gray, and others (1987) shows how this fingerprinting methodology can be applied to trace the offset of lithotectonic (or lithostratigraphic as labeled by some authors) terranes.The lead isotope data presented in table 1 represent the work completed on sulfide mineral deposits located in the Russian Far East from 1993 to 1995, when this study was terminated due to lack of funding. The lead isotope data are reported here for use by investigators who may find them of value in mineral exploration. No attempt is made to summarize the voluminous literature on these mineral deposits.

Data Series↗
USGS2020

Geologic map and borehole stratigraphy of Hinkley Valley and vicinity, San Bernardino County, California

Hinkley Valley, in the central to western Mojave Desert of southeastern California, has a long historical record owing to its position as a crossroads for rail and road traffic and its position adjacent to the Mojave River. Subflow in the Mojave River provided groundwater recharge that maintained water consumption and demand by way of shallow wells for local agriculture in the valley. Its crossroads position led to construction of several power-transmission lines, pipeline, and communications cable routes that transect Hinkley Valley. One of these, a natural gas pipeline and its associated compressor station, was the locus of hexavalent chromium, Cr(VI), released into, and consequent contamination of, groundwater. Understanding the movement and fate of the contaminants is a complex hydrologic and geochemical problem. Geologic mapping of the Hinkley Valley area provides framework elements for use in resolving this problem. This report provides new information on surface and subsurface geology to better constrain the origin and geometry of hydrologically important deposits in the Hinkley Valley area and describes youthful faults that may control sediment distribution and groundwater flow. The geologic map (sheet 1) presents substantial new information on surficial geology, including Pliocene deposits, but does not contain significant new work on bedrock. Bedrock investigations were specific to identifying youthful faults and representative outcrops for rocks that were penetrated by boreholes in the valley. Special attention was placed on locating and describing youthful faults. In addition, we analyzed gravity data to (1) map horizontal gradients that we interpret to reflect long-term fault traces and to (2) estimate the depth to bedrock, which is defined as Miocene and older intrusive and metamorphic rocks for the purposes of this report. The subsurface geology of Hinkley Valley was investigated by examining borehole sediment cores and rock encountered at the base of the sediment section. We analyzed the core to determine depositional environments, provenance, and age of the sediment that infilled the valley. Valleys, mountains, and basins in the Hinkley Valley area are topographically complex and incompletely named. The nearly flat floored Hinkley Valley slopes gently northward. It is framed by Mount General and the informally named “Hinkley hills” (southeast of Mount General) on the northeast and by Iron Mountain and Lynx Cat Mountain on the southwest, although breaks in the western mountains allow stream connections between Hinkley Valley and another valley to the west that is herein referred to as Hawes valley. At its south end, Hinkley Valley is traversed by the entrenched Mojave River, which passes east out of the valley past Barstow. North of Hinkley Valley, a few low hills (including Red Hill) separate the valley from a broad west-sloping piedmont that is part of the physiographic Harper Basin (of which the Harper Lake playa is the center). The lower part of this piedmont, however, is referred to as Water Valley, although it is not a distinct valley. The name derives from groundwater sourced from subflow in the Mojave River, which caused shallow water and even artesian flow in Water Valley but not in other parts of the Harper Basin. When water filled the Harper Basin to form Pleistocene Lake Harper it not only submerged Water Valley but also northern Hinkley Valley.

California↗
USGS2015

Water quality of the Little Arkansas River and Equus Beds Aquifer before and concurrent with large-scale artificial recharge, south-central Kansas, 1995-2012

The city of Wichita artificially recharged about 1 billion gallons of water into the Equus Beds aquifer during 2007–2012 as part of Phase I recharge of the Artificial Storage and Recovery project. This report, prepared in cooperation by the U.S. Geological Survey and the city of Wichita, Kansas, summarizes Little Arkansas River (source-water for artificial recharge) and Equus Beds aquifer water quality before (1995–2006) and during (2007–2012) Artificial Storage and Recovery Phase I recharge. Additionally, aquifer water-quality distribution maps are presented and water-quality changes associated with Phase I recharge timing are described. Computed chloride concentrations in the Little Arkansas River exceeded the Federal secondary maximum contaminant level (SMCL) about 20 percent of the time during 1999 through 2012, primarily during low-flow conditions. Groundwater chloride concentrations during 2001 through 2012 exceeded the SMCL in about 6 percent of shallow wells and 7 percent of deep wells, primarily near Burrton, Kansas and along the Arkansas River. Nearly all surface water nitrate plus nitrite concentrations during 1995 through 2012 were less than the Federal maximum contaminant level (MCL); groundwater nitrate plus nitrite concentrations exceeded the MCL in about 16 percent of shallow groundwater samples and were minimal in the deeper parts of the aquifer. Several trace elements frequently exceeded drinking water criteria, including arsenic, iron, and manganese. Recharge activities at Phase I recharge wells have not resulted in substantial effects on groundwater quality in the area, likely because the total amount of water recharged is relatively small (1 billion gallons) compared to aquifer storage volume (greater than 990 billion gallons in winter 2012). The eastward movement of the Burrton chloride plume is likely being slowed by a line of recharge locations associated with Phase I; however, chloride concentrations in deep groundwater still advanced to less than one half mile from the central part of the study area. Water-quality constituents of concern (major ions, nutrients, trace elements, triazine herbicides, and fecal indicator bacteria) have not increased substantially and are likely more affected by climatological (natural recharge by precipitation) and natural (geochemical oxidation/reduction, metabolic and decay rates) processes than artificial recharge. Arsenic remains a water-quality constituent of concern because of natural and continued persistence of concentrations exceeding the Federal maximum contaminant level of 10 micrograms per liter, especially in the deeper parts of the Equus Beds aquifer.

Kansas↗
USGS1987

Hydrologic monitoring of selected streams in coal fields of central and southern Utah — Summary of data collected, August 1978-September 1984

The U.S. Geological Survey conducted a coal-hydrology monitoring program in coal-field areas of central and southern Utah during August 1978-September 1984 to determine possible hydrologic impacts of future mining and to provide a better understanding of the hydrologic systems of the coal resource areas monitored. Data were collected at 19 gaging stations--18 stations in the Price, San Rafael, and Dirty Devil River basins, and 1 in the Kanab Creek Basin. Streamflow data were collected continuously at 11 stations and seasonally at 5 stations. At the other three stations streamflow data were collected continuously during the 1979 water year and then seasonally for the rest of their periods of record. Types of data collected at each station included quantity and quality of streamflow; suspended sediment concentrations; and descriptions of stream bottom sediments, benthic invertebrate, and phytoplankton samples. Also, base flow measurements were made annually upstream from 12 of the gaging stations. Stream bottom sediment sampled at nearly all the monitoring sites contained small to moderate quantities of coal, which may be attributed chiefly to pre-monitoring mining. Streamflow sampled at several sites contained large concentrations of sulfate and dissolved solids. Also, concentrations of various trace elements at 10 stations, and phenols at 18 stations, exceeded the criteria of the EPA for drinking water. This may be attributed to contemporary (water years 1979-84) mine drainage activities. The data collected during the complete water years (1979-84) of monitoring do provide a better understanding of the hydrologic systems of the coal field areas monitored. The data also provide a definite base by which to evaluate hydrologic impacts of continued or increased coal mining in those areas. (Author 's abstract)

Utah↗
USGS2000

Water quality at basic fixed sites in the Upper Colorado River basin National Water-Quality Assessment study unit, October 1995-September 1998

The Upper Colorado River Basin study unit of the U.S. Geological Survey National Water-Quality Assessment Program consists of the Colorado River watershed upstream from near the Colorado-Utah State line. The basin is about equally divided between the Southern Rocky Mountains and the Colorado Plateau physiographic provinces. Data were collected at pairs of indicator sites for mining, increasing urban development, and agricultural land use. Reference basic fixed sites were established in each physiographic province to provide baseline or background information in areas where anthropogenic influences are minimal. Water-quality data collection began at three of the sites in water year 1995. Full implementation of data collection at the 14-site network began in October 1996 and continued through September 1998. Six hundred and sixty water-quality samples were collected at the network sites. Snowmelt runoff dominates the hydrology in most of the basin, but water management for irrigation, storage, and transmountain diversions substantially changes annual runoff characteristics in some areas. Streamflow during water years 1995 and 1997 was generally greater than long-term average conditions. During water year 1996, streamflow also was above average at many sites but not to the extent as seen during 1995 or 1997. Water year 1998 streamflows typically were near or slightly below the long-term average. Extreme low-flow conditions generally did not occur at the sites during the data-collection period. Dissolved nitrate and total phosphorus concentrations at the background site within the Southern Rocky Mountain physiographic province typically were low (hundreths of milligrams per liter). Concentrations in areas of urban development and areas in the lower parts of the basin generally were in the tenths of milligrams per liter and in some agricultural areas were in the milligram per liter range. Median dissolved-solids concentrations at sites in the Southern Rocky Mountains were typically less than 200 milligrams per liter. Small tributaries in the Colorado Plateau and agricultural areas had dissolved-solids concentrations in the thousands of milligrams per liter range. Trace-element concentrations were high, at times, in areas of mining land use. Median zinc concentration for the French Gulch near Breckenridge site was 2,700 micrograms per liter. Comparison of measured concentrations to Colorado State instream standards showed that concentrations of dissolved oxygen, pH, nitrate, and ammonia were within instream standards at all sites. Concentrations of cadmium and zinc at the site on French Gulch (a mining-affected site) often were greater than the State instream standard.

Colorado↗