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John G. Schumacher

Publications and source records attributed to John G. Schumacher.

At least 19 recordsLinked to original sources
USGS2020

Technical memorandum: Compound specific isotope analysis, Oak Grove Village well site OU1, Franklin County, Missouri

A study involving Compound Specific Isotope Analysis (CSIA) of trichloroethene (TCE) in groundwater at the Oak Grove Village (OGV) Well Site was conducted by the U.S. Environmental Protection Agency (EPA) in 2014 in an effort to fingerprint the source(s). This technical memorandum, written as a joint effort between HydroGeoLogic, Inc. (HGL) and the U.S. Geological Survey (USGS) Central Midwest Water Science Center (Schumacher, 2019), documents the procedures and analysis of the CSIA investigation. CSIA is an analytical method that measures the isotopic ratios of naturally occurring stable isotopes in specific chemical compounds in environmental samples. CSIA using primarily the ratio of carbon 13 C/ 12 C (δ 13 C), known as 1-D CSIA, has been used for decades in evaluating degradation pathways of organic compounds, including chlorinated solvents such as TCE. Ratios of stable chlorine isotopes 37 Cl/ 35 Cl (δ 37 Cl) also have been used with carbon isotopes, collectively known as 2-D CSIA, and most recently isotopes of hydrogen 2 H/ 1 H (δ 2 H) have been added, collectively known as 3-D CSIA, in attempts to further determine source, transport, and fate of compounds such as TCE (Ertl et al., 1998; Hunkeler et al., 2011; Kuder et al., 2013; McHugh et al., 2011; Shouakar-Stash et al., 2003; EPA, 2008; and van Warmerdam et al., 1995.

Missouri↗
USGS2018

Distribution of mining-related trace elements in streambed and flood-plain sediment along the middle Big River and tributaries in the Southeast Missouri Barite District, 2012–15

Lead mining first began in the Big River watershed during the 1700s. Lead was the primary metal mined throughout most of the 1700s and early 1800s and it continued to be mined until the mid-1900s. Barite mining began in the middle part of the watershed in the mid- to late 1800s. Although considerable attention has been given to concentrations of miningrelated trace elements (mostly cadmium, lead, and zinc) in the Big River and its tributaries draining the Old Lead Belt, there is less information regarding concentrations of mining-related trace elements in tributaries draining the Barite District in southeast Missouri, which is downstream from the Old Lead Belt, and the contribution of sediment transported from this district to trace elements in lower reaches of the Big River. The purpose of this report is to present results of an investigation of the distribution of mining-related trace elements in sediments in the middle reach of the Big River downstream from the Old Lead Belt and the Big River tributaries that drain a large part of the Barite District. In general, concentrations of cadmium and lead in streambed sediment were largest in samples from the Big River and smallest in Barite District tributary samples. Concentrations of zinc were somewhat similar in the Big River and Barite District tributaries; however, higher concentrations were present in upstream Big River site samples, as well as in samples from one site on Maddin Creek and at another site on Old Mines Creek that drains the Barite District. Barium concentrations were considerably larger in samples from Barite District tributaries compared to samples collected on the Big River. Samples collected downstream from the Barite District on the Big River had considerably larger barium concentrations than samples collected upstream from the Barite District. Flood-plain core samples were collected from 26 cores at 5 transect locations along tributaries in the Barite District. Of the individual 693 bulk (unsieved) samples from these cores analyzed by x-ray fluorescence, the probable effects concentration (PEC) values were exceeded for cadmium (PEC of 4.98 milligrams per kilogram [mg/kg], 218 samples), lead (PEC of 128 mg/kg, 91 samples), nickel (PEC of 48.6 mg/kg, 45 samples), and zinc (PEC of 459 mg/kg, 77 samples). Of the 693 samples, 21 exceeded the U.S. Environmental Protection Agency residential yard cleanup level of 400 mg/kg for lead; 19 of these were samples from a single transect near the mouth of Mineral Fork Creek where its flood plain joins the Big River flood plain. Shortly after the December 2015 flood on the Big River (the third largest flood along the river since the 1950s), 23 samples of fine sediment deposited from the flood were collected from the Big River flood plain upstream and downstream from the Barite District and several tributaries. Overall, the general pattern of barium, lead, and zinc concentrations in the 2015 flood sediment samples was similar to that observed in the streambed-sediment samples. Overall concentrations of barium were larger at Big River sites downstream from the Barite District, and cadmium, lead, and zinc concentrations were generally similar or smaller at sites downstream from the Barite District when compared to sites upstream from the Barite District. These data indicate a substantial influx of barium from the Barite District into the Big River but only a minimal influx of cadmium, lead, and zinc.

Missouri↗
USGS2017

Contaminant gradients in trees: Directional tree coring reveals boundaries of soil and soil-gas contamination with potential applications in vapor intrusion assessment

Contaminated sites pose ecological and human-health risks through exposure to contaminated soil and groundwater. Whereas we can readily locate, monitor, and track contaminants in groundwater, it is harder to perform these tasks in the vadose zone. In this study, tree-core samples were collected at a Superfund site to determine if the sample-collection location around a particular tree could reveal the subsurface location, or direction, of soil and soil-gas contaminant plumes. Contaminant-centroid vectors were calculated from tree-core data to reveal contaminant distributions in directional tree samples at a higher resolution, and vectors were correlated with soil-gas characterization collected using conventional methods. Results clearly demonstrated that directional tree coring around tree trunks can indicate gradients in soil and soil-gas contaminant plumes, and the strength of the correlations were directly proportionate to the magnitude of tree-core concentration gradients (spearman’s coefficient of -0.61 and -0.55 in soil and tree-core gradients, respectively). Linear regression indicates agreement between the concentration-centroid vectors is significantly affected by in-planta and soil concentration gradients and when concentration centroids in soil are closer to trees. Given the existing link between soil-gas and vapor intrusion, this study also indicates that directional tree coring might be applicable in vapor intrusion assessment.

Missouri↗
USGS2017

Tree sampling as a method to assess vapor intrusion potential at a site characterized by VOC-contaminated groundwater and soil

Vapor intrusion (VI) by volatile organic compounds (VOCs) in the built environment presents a threat to human health. Traditional VI assessments are often time-, cost-, and labor-intensive; whereas traditional subsurface methods sample a relatively small volume in the subsurface and are difficult to collect within and near structures. Trees could provide a similar subsurface sample where roots act as the “sampler’ and are already onsite. Regression models were developed to assess the relation between PCE concentrations in over 500 tree-core samples with PCE concentrations in over 50 groundwater and 1000 soil samples collected from a tetrachloroethylene- (PCE-) contaminated Superfund site and analyzed using gas chromatography. Results indicate that in planta concentrations are significantly and positively related to PCE concentrations in groundwater samples collected at depths less than 20 m (adjusted R 2 values greater than 0.80) and in soil samples (adjusted R 2 values greater than 0.90). Results indicate that a 30 cm diameter tree characterizes soil concentrations at depths less than 6 m over an area of 700–1600 m 2 , the volume of a typical basement. These findings indicate that tree sampling may be an appropriate method to detect contamination at shallow depths at sites with VI.

Missouri↗
USGS2016

Persistence and microbial source tracking of Escherichia coli at a swimming beach at Lake of the Ozarks State Park, Missouri

The Missouri Department of Natural Resources (MDNR) has closed or posted advisories at public beaches at Lake of the Ozarks State Park in Missouri because of Escherichia coli ( E. coli ) concentration exceedances in recent years. Spatial and temporal patterns of E. coli concentrations, microbial source tracking, novel sampling techniques, and beach-use patterns were studied during the 2012 recreational season to identify possible sources, origins, and occurrence of E. coli contamination at Grand Glaize Beach (GGB). Results indicate an important source of E. coli contamination at GGB was E. coli released into the water column by bathers resuspending avian-contaminated sediments, especially during high-use days early in the recreational season. Escherichia coli concentrations in water, sediment, and resuspended sediment samples all decreased throughout the recreational season likely because of decreasing lake levels resulting in sampling locations receding away from the initial spring shoreline as well as natural decay and physical transport out of the cove. Weekly MDNR beach monitoring, based solely on E. coli concentrations, at GGB during this study inaccurately predicted E. coli exceedances, especially on weekends and holidays. Interestingly, E. coli of human origin were measured at concentrations indicative of raw sewage in runoff from an excavation of a nearby abandoned septic tank that had not been used for nearly two years.

Missouri↗
USGS2014

Occurrence and origin of Escherichia coli in water and sediments at two public swimming beaches at Lake of the Ozarks State Park, Camden County, Missouri, 2011-13

In the past several years, the Missouri Department of Natural Resources has closed two popular public beaches, Grand Glaize Beach and Public Beach 1, at Lake of the Ozarks State Park in Osage Beach, Missouri when monitoring results exceeded the established Escherichia coli (E. coli) standard. As a result of the beach closures, the U.S. Geological Survey and Missouri University of Science and Technology, in cooperation with the Missouri Department of Natural Resources, led an investigation into the occurrence and origins of E. coli at Grand Glaize Beach and Public Beach 1. The study included the collection of more than 1,300 water, sediment, and fecal source samples between August 2011 and February 2013 from the two beaches and vicinity. Spatial and temporal patterns of E. coli concentrations in water and sediments combined with measurements of environmental variables, beach-use patterns, and Missouri Department of Natural Resources water-tracing results were used to identify possible sources of E. coli contamination at the two beaches and to corroborate microbial source tracking (MST) sampling efforts. Results from a 2011 reconnaissance sampling indicate that water samples from Grand Glaize Beach cove contained significantly larger E. coli concentrations than adjacent coves and were largest at sites at the upper end of Grand Glaize Beach cove, indicating a probable local source of E. coli contamination within the upper end of the cove. Results from an intensive sampling effort during 2012 indicated that E. coli concentrations in water samples at Grand Glaize Beach cove were significantly larger in ankle-deep water than waist-deep water, trended downward during the recreational season, significantly increased with an increase in the total number of bathers at the beach, and were largest during the middle of the day. Concentrations of E. coli in nearshore sediment (sediment near the shoreline) at Grand Glaize Beach were significantly larger in foreshore samples (samples collected above the shoreline) than in samples collected in ankle-deep water below the shoreline, significantly larger in the left and middle areas of the beach than the right area, and substantially larger than similar studies at E. coli- contaminated beaches on Lake Erie in Ohio. Concentrations of E. coli in the water column also were significantly larger after resuspension of sediments. Results of MST indicate a predominance of waterfowl-associated markers in nearshore sediments at Grand Glaize Beach consistent with frequent observations of goose and vulture fecal matter in sediment, especially on the left and middle areas of the beach. The combination of spatial and temporal sampling and MST indicate that an important source of E. coli contamination at Grand Glaize Beach during 2012 was E. coli released into the water column by bathers resuspending E. coli-contaminated sediments, especially during high-use days early in the recreational season.

Missouri↗
USGS2010

An exploratory investigation of polar organic compounds in waters from a lead–zinc mine and mill complex

Surface water samples were collected in 2006 from a lead mine-mill complex in Missouri to investigate possible organic compounds coming from the milling process. Water samples contained relatively high concentrations of dissolved organic carbon (DOC; greater than 20 mg/l) for surface waters but were colorless, implying a lack of naturally occurring aquatic humic or fulvic acids. Samples were extracted by three different types of solid-phase extraction and analyzed by electrospray ionization/mass spectrometry. Because large amounts of xanthate complexation reagents are used in the milling process, techniques were developed to extract and analyze for sodium isopropyl xanthate and sodium ethyl xanthate. Although these xanthate reagents were not found, trace amounts of the degradates, isopropyl xanthyl thiosulfonate and isopropyl xanthyl sulfonate, were found in most locations sampled, including the tailings pond downstream. Dioctyl sulfosuccinate, a surfactant and process filtering aid, was found at concentrations estimated at 350 μg/l at one mill outlet, but not downstream. Release of these organic compounds downstream from lead-zinc mine and milling areas has not previously been reported. A majority of the DOC remains unidentified.

Missouri↗
USGS2010

Borehole Geophysical, Water-Level, and Water-Quality Investigation of a Monitoring Well Completed in the St. Francois Aquifer in Oregon County, Missouri, 2005-08

A deep (more than 2,000 feet) monitoring well was installed in an area being explored for lead and zinc deposits within the Mark Twain National Forest in southern Missouri. The area is a mature karst terrain where rocks of the Ozark aquifer, a primary source of water for private and public supplies and major springs in the nearby Eleven Point National Wild and Scenic River and the Ozark National Scenic Riverways, are exposed at the surface. The potential lead deposits lie about 2,000 feet below the surface within a deeper aquifer, called the St. Francois aquifer. The two aquifers are separated by the St. Francois confining unit. The monitoring well was installed as part of a series of investigations to examine potentiometric head relations and water-quality differences between the two aquifers. Results of borehole flowmeter measurements in the open borehole and water-level measurements from the completed monitoring well USGS-D1 indicate that a seasonal upward gradient exists between the St. Francois aquifer and the overlying Ozark aquifer from about September through February. The upward potentiometric heads across the St. Francois confining unit that separates the two aquifers averaged 13.40 feet. Large reversals in this upward gradient occurred during the late winter through summer (about February through August) when water levels in the Ozark aquifer were as much as 138.47 feet higher (average of 53.84 feet) than water levels in the St. Francois aquifer. Most of the fluctuation of potentiometric gradient is caused by precipitation and rapid recharge that cause large and rapid increases in water levels in the Ozark aquifer. Analysis of water-quality samples collected from the St. Francois aquifer interval of the monitoring well indicated a sodium-chloride type water containing dissolved-solids concentrations as large as 1,300 milligrams per liter and large concentrations of sodium, chloride, sulfate, boron, and lithium. In contrast, water in the overlying Ozark aquifer interval of the monitoring well was a calcium-magnesium-bicarbonate type water containing less than 250 milligrams per liter dissolved solids and substantially smaller concentrations of major and trace elements.

Scientific Investigations Report↗
USGS2009

Geohydrologic Investigations and Landscape Characteristics of Areas Contributing Water to Springs, the Current River, and Jacks Fork, Ozark National Scenic Riverways, Missouri

The Ozark National Scenic Riverways (ONSR) is a narrow corridor that stretches for approximately 134 miles along the Current River and Jacks Fork in southern Missouri. Most of the water flowing in the Current River and Jacks Fork is discharged to the rivers from springs within the ONSR, and most of the recharge area of these springs is outside the ONSR. This report describes geohydrologic investigations and landscape characteristics of areas contributing water to springs and the Current River and Jacks Fork in the ONSR. The potentiometric-surface map of the study area for 2000-07 shows that the groundwater divide extends beyond the surface-water divide in some places, notably along Logan Creek and the northeastern part of the study area, indicating interbasin transfer of groundwater between surface-water basins. A low hydraulic gradient occurs in much of the upland area west of the Current River associated with areas of high sinkhole density, which indicates the presence of a network of subsurface karst conduits. The results of a low base-flow seepage run indicate that most of the discharge in the Current River and Jacks Fork was from identified springs, and a smaller amount was from tributaries whose discharge probably originated as spring discharge, or from springs or diffuse groundwater discharge in the streambed. Results of a temperature profile conducted on an 85-mile reach of the Current River indicate that the lowest average temperatures were within or downstream from inflows of springs. A mass-balance on heat calculation of the discharge of Bass Rock Spring, a previously undescribed spring, resulted in an estimated discharge of 34.1 cubic feet per second (ft3/s), making it the sixth largest spring in the Current River Basin. The 13 springs in the study area for which recharge areas have been estimated accounted for 82 percent (867 ft3/s of 1,060 ft3/s) of the discharge of the Current River at Big Spring during the 2006 seepage run. Including discharge from other springs, the cumulative discharge from springs was over 90 percent of the river discharge at most of the spring locations, and was 92 percent at Big Spring and at the lower end of the ONSR. The discharge from the 1.9-mile long Pulltite Springs Complex measured in the 2006 seepage run was 88 ft3/s. Most of this (77 ft3/s) was from the first approximately 0.25 mi of the Pulltite Springs Complex. It has been estimated that the annual mean discharge from the Current River Springs Complex is 125 ft3/s, based on an apparent discharge of 50 ft3/s during a 1966 U.S. Geological Survey seepage run. However, a reinterpretation of the 1966 seepage run data shows that the discharge from the Current River Springs Complex instead was about 12.6 ft3/s, and the annual mean discharge was estimated to be 32 ft3/s, substantially less than 125 ft3/s. The 2006 seepage run showed a gain of only 12 ft3/s from the combined Round Spring and Current River Springs Complex from the mouth of Sinking Creek to 0.7 mi upstream from Root Hollow. The 2006 temperature profile measurements did not indicate any influx of spring discharge throughout the length of the Current River Springs Complex. The spring recharge areas with the largest number of identified sinkholes are Big Spring, Alley Spring, and Welch Spring. The spring recharge areas with the largest number of sinkholes per square mile of recharge area are Alley Spring, Blue Spring (Jacks Fork), Welch Spring, and Round Spring and the Current River Springs Complex. Using the currently known locations of losing streams, the Big Spring recharge area has the largest number of miles of losing stream, and the Bass Rock Spring recharge area has the largest number of miles of losing stream per unit recharge area. The spring recharge areas with the most open land and the least forested land per unit recharge area are Blue Spring (Jacks Fork), Welch Spring, Montauk Springs, and Alley Spring. The spring recharge areas with the least amount

Scientific Investigations Report↗
USGS2008

Hydrologic investigations concerning lead mining issues in southeastern Missouri

Good stewardship of our Nation's natural resources demands that the extraction of exploitable, minable ore deposits be conducted in harmony with the protection of the environment, a dilemma faced by many land and water management agencies in the Nation's mining areas. As ore is mined, milled, and sent to the smelter, it leaves footprints where it has been in the form of residual trace metals. Often these footprints become remnants that can be detrimental to other natural resources. This emphasizes the importance of understanding the earth's complex physical and biological processes and their interactions at increasingly smaller scales because subtle changes in one component can substantially affect others. Understanding these changes and resulting effects requires an integrated, multidisciplinary scientific approach. As ore reserves are depleted in one area, additional exploitable deposits are required to replace them, and at times these new deposits are discovered in previously unmined areas. Informed decisions concerning resource management in these new, proposed mining areas require an understanding of the potential consequences of the planned mining actions. This understanding is usually based on knowledge that has been accumulated from studying previously mined areas with similar geohydrologic and biologic conditions. If the two areas experience similar mining practices, the information should be transferable. Lead and zinc mining along the Viburnum Trend Subdistrict of southeastern Missouri has occurred for more than 40 years. Additional potentially exploitable deposits have been discovered 30 miles to the south, within the Mark Twain National Forest. It is anticipated that the observation of current (2008) geohydrologic conditions in the Viburnum Trend can provide insight to land managers that will help reasonably anticipate the potential mining effects should additional mining occur in the exploration area. The purpose of this report is to present a compilation of previously unpublished information that was collected as part of a larger multidisciplinary study of lead mining issues in southeastern Missouri. The report resulted from the application of a multidisciplinary approach to investigate current hydrologic and biologic conditions in streams of the Viburnum Trend and the exploration area in the Mark Twain National Forest.

Missouri↗
USGS2007

Recharge area, base-flow and quick-flow discharge rates and ages, and general water quality of Big Spring in Carter County, Missouri, 2000-04

Exploration for lead deposits has occurred in a mature karst area of southeast Missouri that is highly valued for its scenic beauty and recreational opportunities. The area contains the two largest springs in Missouri (Big Spring and Greer Spring), both of which flow into federally designated scenic rivers. Concerns about potential mining effects on the area ground water and aquatic biota prompted an investigation of Big Spring. Water-level measurements made during 2000 helped define the recharge area of Big Spring, Greer Spring, Mammoth Spring, and Boze Mill Spring. The data infer two distinct potentiometric surfaces. The shallow potentiometric surface, where the depth-to-water is less than about 250 feet, tends to mimic topographic features and is strongly controlled by streams. The deep potentiometric surface, where the depth-to-water is greater than about 250 feet represents ground-water hydraulic heads within the more mature karst areas. A highly permeable zone extends about 20 mile west of Big Spring toward the upper Hurricane Creek Basin. Deeper flowing water in the Big Spring recharge area is directed toward this permeable zone. The estimated sizes of the spring recharge areas are 426 square miles for Big Spring, 352 square miles for Greer Spring, 290 square miles for Mammoth Spring, and 54 square miles for Boze Mill Spring. A discharge accumulation curve using Big Spring daily mean discharge data shows no substantial change in the discharge pattern of Big Spring during the period of record (water years 1922 through 2004). The extended periods when the spring flow deviated from the trend line can be attributed to prolonged departures from normal precipitation. The maximum possible instantaneous flow from Big Spring has not been adequately defined because of backwater effects from the Current River during high-flow conditions. Physical constraints within the spring conduit system may restrict its maximum flow. The largest discharge measured at Big Spring during the period of record (water years 1922 through 2004) was 1,170 cubic feet per second on December 7, 1982. The daily mean water temperature of Big Spring was monitored during water years 2001 through 2004 and showed little variability, ranging from 13 to 15° C (degree Celsius). Water temperatures generally vary less than 1° C throughout the year. The warmest temperatures occur during October and November and decrease until April, indicating Big Spring water temperature does show a slight seasonal variation. The use of the traditional hydrograph separation program HYSEP to determine the base flow and quick flow or runoff components at Big Spring failed to yield base-flow and quick-flow discharge curves that matched observations of spring characteristics. Big Spring discharge data were used in combination with specific conductance data to develop an improved hydrograph separation method for the spring. The estimated annual mean quick flow ranged from 15 to 48 cubic feet per second for the HYSEP analysis and ranged from 26 to 154 cubic feet per second for the discharge and specific conductance method for water years 2001 to 2004. Using the discharge and specific conductance method, the estimated base-flow component rises abruptly as the spring hydrograph rises, attains a peak value on the same day as the discharge peak, and then declines abruptly from its peak value. Several days later, base flow begins to increase again at an approximately linear trend, coinciding with the time at which the percentage of quick flow has reached a maximum after each recharge-induced discharge peak. The interval between the discharge peak and the peak in percentage quick flow ranges from 8 to 11 days for seven hydrograph peaks, consistent with quick-flow traveltime estimates by dye-trace tests from the mature karst Hurricane Creek Basin in the central part of the recharge area. Concentrations of environmental tracers chlorofluorocarbons (CFCs: CFC-11, CFC-12, CFC-113), and sulfur hexafluoride in discharge from Big Spring vary approximately linearly with percent quick flow from about 5 to 45 percent of discharge. Linear extrapolation to 100 percent quick flow implies CFC and SF 6 concentrations nearly identical to those in the 2002 atmosphere and indicates a modern age for the quick-flow component. Tracer concentrations for less than about 5 percent quick flow are increasingly lower than those expected from linear extrapolation to zero percent quick flow, indicating that the reservoir of older water in the Big Spring watershed may be a series of water mixtures with piston-flow ages greater than those obtained by extrapolation to zero percent quick flow. Each sample point with a low percentage of quick flow (less than 5 percent) may be a unique mixture. Environmental tracer data from Big Spring plot intermediate to the simple binary mixing of modern and old, pre-tracer water and results from the exponential mixture model. The mean ages of waters in the base-flow component approximately range from 30 to 200 years. The mean age of the base-flow component is youngest (30 to 40 years) in samples containing the highest quick-flow component (45 percent quick flow) and increases to 200 years or more as the fraction of quick flow decreases to less than 5 percent. Tritium data are consistent with a model of dilution of a modern component with an old, pre-tracer component and indicates that the old fraction is mostly pre-1960s in age with mean residence time of more than several hundred years. All of the samples from Big Spring and Greer Spring have water temperatures warmer than their nitrogen-argon recharge temperature, which range from approximately 10.5 to 14° C, suggesting recharge to the Big Spring watershed occurs primarily in late winter to early spring. The water temperatures at Big Spring are consistent with relatively shallow circulation (less than about 600 feet), and the water does not appear to be warmed by deep circulation along a geothermal gradient. Specific conductance values and concentrations of most inorganic constituents in water samples from Big Spring generally decrease with increasing discharge because of dilution with quick-flow water of lower ionic strength. Concentrations of some constituents such as chloride and nitrite plus nitrate, and fecal coliform densities, however, did not decrease with increasing discharge, indicating that quick flow probably is a more important source of these constituents compared to base flow. Water samples from Big Spring plot along the line of dolomite dissolution by carbonic acid, are at equilibrium with dolomite and calcite, and have a molar ratio of Ca:Mg of near 1, indicating dissolution of the mineral dolomite as the primary control on concentrations of calcium, magnesium, and bicarbonate. The flux of calcium and magnesium from Big Spring represents the dissolution of about 1,950 cubic feet of dolomite per day. The suspended sediment load of Big Spring was estimated to range from about 1 to about 70 tons per day, and the sediment load during base-flow periods ranged from about 1 to about 7 tons per day.

Missouri↗
USGS2007

Water and Streambed-Sediment Quality in the Upper Elk River Basin, Missouri and Arkansas, 2004-06

The U.S. Geological Survey, in cooperation with the Missouri Department of Natural Resources, collected water and streambedsediment samples in the Upper Elk River Basin in southwestern Missouri and northwestern Arkansas from October 2004 through December 2006. The samples were collected to determine the stream-water quality and streambed-sediment quality. In 1998, the Missouri Department of Natural Resources included a 21.5-mile river reach of the Elk River on the 303(d) list of impaired waters in Missouri as required by Section 303(d) of the Federal Clean Water Act. The Elk River is on the 303(d) list for excess nutrient loading. The total phosphorus distribution by decade indicates that the concentrations since 2000 have increased significantly from those in the 1960s, 1980s, and 1990s. The nitrate as nitrogen (nitrate) concentrations also have increased significantly in post-1985 from pre-1985 samples collected at the Elk River near Tiff City. Concentrations have increased significantly since the 1960s. Concentrations in the 1970s and 1980s, though similar, have increased from those in the 1960s, and the concentrations from the 1990s and 2000s increased still more. Nitrate concentrations significantly increased in samples that were collected during large discharges (greater than 355 cubic feet per second) from the Elk River near Tiff City. Nitrate concentrations were largest in Indian Creek. Several sources of nitrate are present in the basin, including poultry facilities in the upper part of the basin, effluent inflow from communities of Anderson and Lanagan, land-applied animal waste, chemical fertilizer, and possible leaking septic systems. Total phosphorus concentrations were largest in Little Sugar Creek. The median concentration of total phosphorus from samples from Little Sugar Creek near Pineville was almost four times the median concentration in samples from the Elk River near Tiff City. Median concentrations of nutrient species were greater in the stormwater samples than the median concentrations in the ambient samples. Nitrate concentrations in stormwater samples ranged from 133 to 179 percent of the concentration in the ambient samples. The total phosphorus concentrations in the stormwater samples ranged from about 200 to more than 600 percent of the concentration in the ambient samples. Base-flow conditions as reflected by the seepage run of the summer of 2006 indicate that 52 percent of the discharge at the Elk River near Tiff City is contributed by Indian Creek. Little Sugar Creek contributes 32 percent and Big Sugar Creek 9 percent of the discharge in the Elk River near Tiff City. Only about 7 percent of the discharge at Tiff City comes from the mainstem of the Elk River. Concentrations of dissolved ammonia plus organic nitrogen as nitrogen, dissolved ammonia as nitrogen, dissolved phosphorus, and dissolved orthophosphorus were detected in all streambed-sediment leachate samples. Concentrations of leachable nutrients in streambed-sediment samples generally tended to be slightly larger along the major forks of the Elk River as compared to tributary sites, with sites in the upper reaches of the major forks having among the largest concentrations. Concentrations of leachable nutrients in the major forks generally decreased with increasing distance downstream.

Scientific Investigations Report↗
USGS2004

Assessment of subsurface chlorinated solvent contamination using tree cores at the front street site and a former dry cleaning facility at the Riverfront Superfund site, New Haven, Missouri, 1999-2003

Tree-core sampling has been a reliable and inexpensive tool to quickly assess the presence of shallow (less than about 30 feet deep) tetrachloroethene (PCE) and trichloroethene (TCE) contamination in soils and ground water at the Riverfront Superfund Site. This report presents the results of tree-core sampling that was successfully used to determine the presence and extent of chlorinated solvent contamination at two sites, the Front Street site (operable unit OU1) and the former dry cleaning facility, that are part of the overall Riverfront Superfund Site. Traditional soil and ground-water sampling at these two sites later confirmed the results from the tree-core sampling. Results obtained from the tree-core sampling were used to design and focus subsequent soil and ground-water investigations, resulting in substantial savings in time and site assessment costs. The Front Street site is a small (less than 1-acre) site located on the Missouri River alluvium in downtown New Haven, Missouri, about 500 feet from the south bank of the Missouri River. Tree-core sampling detected the presence of subsurface PCE contamination at the Front Street site and beneath residential property downgradient from the site. Core samples from trees at the site contained PCE concentrations as large as 3,850 mg-h/kg (micrograms in headspace per kilogram of wet core) and TCE concentrations as large as 249 mg-h/kg. Soils at the Front Street site contained PCE concentrations as large as 6,200,000 mg/kg (micrograms per kilogram) and ground-water samples contained PCE concentrations as large as 11,000 mg/L (micrograms per liter). The former dry cleaning facility is located at the base of the upland that forms the south bank of the Missouri River alluvial valley. Tree-core sampling did not indicate the presence of PCE or TCE contamination at the former dry cleaning facility, a finding that was later confirmed by the analyses of soil samples collected from the site. The lateral extent of PCE contamination in trees was in close agreement with the extent of subsurface PCE contamination determined using traditional soil and ground-water sampling methods. Trees growing in soils containing PCE concentrations of 60 to 5,700 mg/kg or larger or overlying ground water containing PCE concentrations from 5 to 11,000 mg/L generally contained detectable concentrations of PCE. The depth to contaminated ground water was about 20 to 25 feet below the land surface. Significant quantitative relations [probability (p) values of less than 0.05 and correlation coefficient (r2) values of 0.88 to 0.90] were found between PCE concentrations in trees and subsurface soils between 4 and 16 feet deep. The relation between PCE concentrations in trees and underlying ground water was less apparent (r2 value of 0.17) and the poor relation is thought to be the result of equilibrium with PCE concentrations in soil and vapor in the unsaturated zone. Based on PCE concentrations detected in trees at the Front Street site and trees growing along contaminated tributaries in other operable units, and from field hydroponic experiments using hybrid poplar cuttings, analysis of tree-core samples appears to be able to detect subsurface PCE contamination in soils at levels of several hundred micrograms per liter or less and PCE concentrations in the range of 8 to 30 mg/L in ground water in direct contact with the roots. Loss of PCE from tree trunks by diffusion resulted in an exponential decrease in PCE concentrations with increasing height above the land surface in most trees. The rate of loss also appeared to be a function of the size and growth characteristics of the tree as some trees exhibited a linear loss with increasing height. Diffusional loss of PCE in small (0.5-inch diameter) trees was observed to occur at a rate more than 10 times larger than in trees 6.5 inches in diameter. Concentrations of PCE also exhibited directional variability around the tree trunks and concentration differe

Scientific Investigations Report↗
USGS2003

Survival, transport, and sources of fecal bacteria in streams and survival in land-applied poultry litter in the upper Shoal Creek basin, southwestern Missouri, 2001–2002

Densities of fecal coliform bacteria along a 5.7-mi (mile) reach of Shoal Creek extending upstream from State Highway 97 (site 3) to State Highway W (site 2) and in two tributaries along this reach exceeded the Missouri Department of Natural Resources (MDNR) standard of 200 col/100 mL (colonies per 100 milliliters) for whole-body contact recreation. A combination of techniques was used in this report to provide information on the source, transport, and survival of fecal bacteria along this reach of Shoal Creek. Results of water-quality samples collected during dye-trace and seepage studies indicated that at summer low base-flow conditions, pastured cattle likely were a substantial source of fecal bacteria in Shoal Creek at the MDNR monitoring site (site 3) at State Highway 97. Using repeat element Polymerase Chain Reaction (rep-PCR), cattle were the presumptive source of about 50 percent of the Escherichia coli ( E. coli ) isolates in water samples from site 3. Cattle, horses, and humans were the most common presumptive source of E. coli isolates at sites further upstream. Poultry was identified by rep-PCR as a major source of E. coli in Pogue Creek, a tributary in the upper part of the study area. Results of the rep-PCR were in general agreement with the detection and distribution of trace concentrations of organic compounds commonly associated with human wastewater, such as caffeine, the antimicrobial agent triclosan, and the pharmaceutical compounds acetaminophen and thiabendazole (a common cattle anthelmintic). Significant inputs of fecal bacteria to Shoal Creek occurred along a 1.6-mi reach of Shoal Creek immediately upstream from site 3. During a 36-hour period in July 2001, average densities of fecal coliform and E. coli bacteria increased from less than or equal to 500 col/100 mL upstream from this stream reach (sample site 2c) to 2,100 and 1,400 col/100 mL, respectively, at the MDNR sampling site. Fecal bacteria densities exhibited diurnal variability at all five sampling sites along the 5.7-mi study reach of Shoal Creek, but the trends at successive downstream sites were out of phase and could not be explained by simple advection and dispersion. At base-flow conditions, the travel time of bacteria in Shoal Creek along the 5.7-mi reach between State Highway W (site 2) and the MDNR sampling site (site 3) was about 26 hours. Substantial dispersion and dilution occurs along the upper 4.1 mi of this reach because of inflows from a number of springs and tributaries and the presence of several long pools and channel meanders. Minimal dispersion and dilution occurs along the 1.6-mi reach immediately upstream from the MDNR sampling site. Measurements of fecal bacteria decay in Shoal Creek during July 2001 indicated that about 8 percent of fecal coliform and E. coli bacteria decay each hour with an average first-order decay constant of 0.084 h -1 (per hour). Results of field test plots indicated that substantial numbers of fecal bacteria present in poul try litter can survive in fields for as much as 8 weeks after the application of the litter to the land surface. Median densities of fecal coliform and E. coli in slurry-water samples collected from fields increased from less than 60 col/100 mL before the application of turkey and broiler litter, to as large as 420,000 and 290,000 col/100 mL after the application of litter. Bacteria densities in the test plots generally decreased in a exponential manner over time with decay rates ranging from 0.085 to 0.185 d -1 (per day) for fecal coliform to between 0.100 and 0.250 d -1 for E. coli . The apparent survival of significant numbers of fecal bacteria on fields where poultry litter has been applied indicates that runoff from these fields is a potential source of fecal bacteria to vicinity streams for many weeks following litter application.

Water-Resources Investigations Report↗