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Robert T. Kay

Publications and source records attributed to Robert T. Kay.

At least 19 recordsLinked to original sources

USGS2022

Water quality in the Missouri River alluvial aquifer near the Independence, Missouri, well field, 1997–2018

Groundwater-quality data collected from 1997 through 2018 from 68 monitoring locations open to the Missouri River alluvial aquifer (hereafter referred to as the “alluvial aquifer”) near the Independence, Missouri, well field were analyzed by the U.S. Geological Survey, in cooperation with the City of Independence, Missouri. This analysis was done to assess the quality of the water in the alluvial aquifer near the well field, identify trends in water quality in the alluvial aquifer from 1997 through 2018, assess hydraulic interaction between the Missouri River and the groundwater system, identify potential threats to the potability of the water extracted from the well field, and identify ways to improve the monitoring effort. Water-quality data indicate that water from the Missouri River recharges the alluvial aquifer. Recharge is exacerbated by pumping from the well field so that the quality of the water pumped from the well field is similar to that of the river for many constituents. Water-quality data indicate that the alluvial aquifer is under oxygen- and nitrate-reducing conditions, and iron- and manganese-reducing conditions are present in most of the alluvial aquifer. Sulfate-reducing conditions are present along the northern and western parts of the monitoring network north of the Missouri River. Maximum contaminant levels for antimony, arsenic, barium, lead, selenium, and uranium were exceeded in at least one sample, and the median concentrations of arsenic exceeded the maximum contaminant level in several monitoring wells on the periphery of the well field. Secondary maximum contaminant levels were exceeded for iron, manganese, and sulfate in multiple wells. Low concentrations of a variety of organic compounds, primarily derived from recharge from the Missouri River with lesser amounts potentially derived from application at land surface in the study area, are present in the alluvial aquifer and in water extracted from the well field.

Missouri↗

USGS2021

Quality of surface water in Missouri, water year 2019

The U.S. Geological Survey, in cooperation with the Missouri Department of Natural Resources, designed and operates a network of monitoring stations on streams and springs throughout Missouri known as the Ambient Water-Quality Monitoring Network (AWQMN). During water year 2019 (October 1, 2018, through September 30, 2019), water-quality data were collected at 73 stations: 71 AWQMN and alternate AWQMN stations, and 2 U.S. Geological Survey National Water Quality Monitoring Program stations. Among the stations in this report, four stations have data presented from additional sampling performed in cooperation with the U.S. Army Corps of Engineers. Summaries of the concentrations of dissolved oxygen, specific conductance, water temperature, suspended solids, suspended sediment, Escherichia coli bacteria, fecal coliform bacteria, dissolved nitrate plus nitrite as nitrogen, total phosphorus, dissolved and total recoverable lead and zinc, and selected pesticides are presented. Most of the stations have been classified based on the physiographic province or primary land use in the watershed monitored by the station. Some stations have been classified based on the unique hydrologic characteristics of the waterbodies (springs, large rivers) they monitor. A summary of hydrologic conditions including peak streamflows, monthly mean streamflows, and 7-day low flows also are presented for representative streamflow-gaging stations in the State.

Missouri↗

USGS2019

Quality of surface water in Missouri, water year 2018

The U.S. Geological Survey, in cooperation with the Missouri Department of Natural Resources, designed and operates a network of monitoring stations on streams and springs throughout Missouri known as the Ambient Water-Quality Monitoring Network. During water year 2018 (October 1, 2017, through September 30, 2018), water-quality data were collected at 76 stations: 74 Ambient Water-Quality Monitoring Network stations and 2 U.S. Geological Survey National Stream Quality Assessment Network stations. Among the 76 stations in this report, 4 stations have data presented from additional sampling performed in cooperation with the U.S. Army Corps of Engineers. Summaries of the concentrations of dissolved oxygen, specific conductance, water temperature, suspended solids, suspended sediment, Escherichia coli bacteria, fecal coliform bacteria, dissolved nitrate plus nitrite as nitrogen, total phosphorus, dissolved and total recoverable lead and zinc, and selected pesticide compounds are presented. Most of the stations have been classified based on the physiographic province or primary land use in the watershed monitored by the station. Some stations have been classified based on the unique hydrologic characteristics of the waterbodies (springs, large rivers) they monitor. A summary of hydrologic conditions including peak streamflows, monthly mean streamflows, and 7-day low flows also are presented for representative streamflow-gaging stations in the State.

Missouri↗

USGS2018

Assessment of water resources in areas that affect the habitat of the endangered Hine’s emerald dragonfly in the Lower Des Plaines River Valley, Illinois

Review of previous investigations indicates that potential decreases in groundwater recharge and increased groundwater extraction in the vicinity of the Lower Des Plaines River Valley in Will County, Illinois, may reduce the amount of groundwater flow in the Silurian aquifer in this area. Groundwater discharge from the Silurian aquifer to wetlands in the Lower Des Plaines River Valley plays an important role in sustaining the habitat of the endangered Hine’s emerald dragonfly (Somatochlora hineana). Groundwater modeling performed by previous investigators indicates that increasing the amount of water pumped from the aquifer in support of expanded quarry operations near the Lockport Prairie Nature Preserve has the potential to reduce groundwater discharge to the most productive Hine’s emerald dragonfly habitats in Illinois, potentially degrading the habitat. Model simulations indicate that mitigation procedures designed to artificially enhance groundwater recharge in the vicinity of dragonfly habitats near the Lockport Prairie Nature Preserve are likely to offset the effects of increased pumping. Several areas with smaller, often intermittent populations of Hine’s emerald dragonflies have been identified in other parts of the Lower Des Plaines River Valley and elsewhere in Illinois. Human activities have the potential to produce changes in hydrology and water quality that can threaten all of these habitats.

Illinois↗

USGS2016

Hydrogeologic framework of LaSalle County, Illinois

Water-supply needs in LaSalle County in northern Illinois are met by surface water and groundwater. Water-supply needs are expected to increase to serve future residential and mining uses. Available information on water use, geology, surface-water and groundwater hydrology, and water quality provides a hydrogeologic framework for LaSalle County that can be used to help plan the future use of the water resources. The Illinois, Fox, and Vermilion Rivers are the primary surface-water bodies in LaSalle County. These and other surface-water bodies are used for wastewater disposal in the county. The Vermilion River is used as a drinking-water supply in the southern part of the county. Water from the Illinois and Fox Rivers also is used for the generation of electric power. Glacial drift aquifers capable of yielding sufficient water for public supply are expected to be present in the Illinois River Valley in the western part of the county, the Troy Bedrock Valley in the northwestern part of the county, and in the Ticona Bedrock Valley in the south-central part of the county. Glacial drift aquifers capable of yielding sufficient water for residential supply are present in most of the county, although well yield often needs to be improved by using large-diameter wells. Arsenic concentrations above health-based standards have been detected in some wells in this aquifer. These aquifers are a viable source for additional water supply in some areas, but would require further characterization prior to full development. Shallow bedrock deposits comprising the sandstone units of the Ancell Group, the Prairie du Chien Group, dolomite of the Galena and Platteville Groups, and Silurian-aged dolomite are utilized for water supply where these units are at or near the bedrock surface or where overlain by Pennsylvanian-aged deposits. The availability of water from the shallow bedrock deposits depends primarily on the geologic unit analyzed. All these deposits can yield sufficient water for residential supply in at least some parts of the county, and sandstone deposits in the Ancell and Prairie du Chien Groups can yield sufficient water for residential or public supply in much of the county. The Cambrian-Ordovician aquifer system comprises the most widespread, productive aquifers in northern Illinois and is used for water supply by a number of municipalities in the county. Water levels in the aquifer system have declined by as much as 300 feet in parts of LaSalle County. The aquifer contains naturally occurring concentrations of radium that are higher than established health guidelines in much of the county.

Illinois↗

USGS2016

Groundwater quality at the Saline Valley Conservancy District well field, Gallatin County, Illinois

The Saline Valley Conservancy District (SVCD) operates wells that supply water to most of the water users in Saline and Gallatin Counties, Illinois. The SVCD wells draw water from a shallow sand and gravel aquifer located in close proximity to an abandoned underground coal mine, several abandoned oil wells, and at least one operational oil well. The aquifer that yields water to the SVCD wells overlies the New Albany Shale, which may be subjected to shale-gas exploration by use of hydraulic fracturing. The SVCD has sought technical assistance from the U.S. Geological Survey to characterize baseline water quality at the SVCD well field so that future changes in water quality (if any) and the cause of those changes (including mine leachate and hydraulic fracturing) can be identified.

Illinois↗

USGS2016

Geology, hydrology, water quality, and potential for interbasin invasive-species spread by way of the groundwater pathway near Lemont, Illinois

Invasive species such as Asian carps have the potential to travel in the egg, larval, or fry stages from the Des Plaines River (DPR) to the Chicago Sanitary and Ship Canal (CSSC) by way of the network of secondary-permeability features in the dolomite aquifer between these water bodies. Such movement would circumvent the electric fish barrier on the canal and allow Asian carps to travel unimpeded into Lake Michigan. This potential pathway for the spread of Asian carps and other invasive species was evaluated by the U.S. Geological Survey. The bed of the DPR appears to be in at least partial contact with the exposed bedrock in most of the area from about 1 mile west of Kingery Highway to Romeo Road (the study area). Areas of exposed bedrock are the most likely places for Asian carps to enter the groundwater system from the DPR. Water levels in the DPR typically are about 7–16 feet higher than those in the CSSC in most of the study area. This difference in water level provides the driving force for the potential spread of Asian carps from the DPR to the CSSC by way of groundwater. Groundwater flow (and potentially invasive-species movement) is through an interconnected network of permeable vertical and horizontal fractures within the Silurian dolomite bedrock. At least some of the fractures are associated with paleo-karst features. Several investigative techniques identified horizontal permeable fractures at about 546–552 feet above the North American Vertical Datum of 1988 within about 55 feet of the CSSC in the focus area between Lemont Road and Interstate 355. The elevation of the bottom of the CSSC in this area is about 551 feet, indicating that a direct conduit for flow of groundwater to the CSSC may be present. Wells further away from the CSSC in this area do not intercept fractures, so the fracture network may not be continuous between the DPR and the CSSC. These data are consistent with field observations of the secondary-permeability network along the CSSC walls, which indicate that the secondary-permeability features are completely filled with Pennsylvanian sediments within a few feet of the canal wall. Water-level data indicate the potential for flow from the DPR into the Silurian aquifer in the focus area, then from the aquifer to the CSSC. Water-level data also indicate that the fractures within the aquifer in the focus area are hydraulically well connected to the CSSC but not to the DPR, indicating that flow from the DPR to the groundwater system may not be substantial or rapid. Water-quality data in the CSSC and the DPR show similar values and trends and are affected by diel and longer term variations in climate and precipitation. However, the values and trends in water quality in the groundwater system tended to be substantially different from those in the DPR and the CSSC, indicating that the DPR and the CSSC do not appreciably recharge the groundwater system. Water-quality and flow data do indicate that groundwater discharges to the CSSC in part of the focus area. The absence of substantial hydraulic interaction between the groundwater and the DPR is supported by the absence of detectable concentrations of the dye tracer added to the DPR in groundwater in the focus area, which indicates that water from the DPR requires more than 2 weeks to move into the monitored parts of the groundwater system under approximately typical hydraulic conditions. The totality of the data indicates that there is minimal potential for the inter-basin spread of Asian carps by way of the groundwater pathway between Romeo Road and Stickney, Illinois.

Illinois↗

USGS2016

Hydrogeology and groundwater quality at monitoring wells installed for the Tunnel and Reservoir Plan System and nearby water-supply wells, Cook County, Illinois, 1995–2013

Groundwater-quality data collected from 1995 through 2013 from 106 monitoring wells open to the base of the Silurian aquifer surrounding the Tunnel and Reservoir Plan (TARP) System in Cook County, Illinois, were analyzed by the U.S. Geological Survey, in cooperation with the Metropolitan Water Reclamation District of Greater Chicago, to assess the efficacy of the monitoring network and the effects of water movement from the tunnel system to the surrounding aquifer. Groundwater from the Silurian aquifer typically drains to the tunnel system so that analyte concentrations in most of the samples from most of the monitoring wells primarily reflect the concentration of the analyte in the nearby Silurian aquifer. Water quality in the Silurian aquifer is spatially variable because of a variety of natural and non-TARP anthropogenic processes. Therefore, the trends in analyte values at a given well from 1995 through 2013 are primarily a reflection of the spatial variation in the value of the analyte in groundwater within that part of the Silurian aquifer draining to the tunnels. Intermittent drainage of combined sewer flow from the tunnel system to the Silurian aquifer when flow in the tunnel systemis greater than 80 million gallons per day may affect water quality in some nearby monitoring wells. Intermittent drainage of combined sewer flow from the tunnel system to the Silurian aquifer appears to affect the values of electrical conductivity, hardness, sulfate, chloride, dissolved organic carbon, ammonia, and fecal coliform in samples from many wells but typically during less than 5 percent of the sampling events. Drainage of combined sewer flow into the aquifer is most prevalent in the downstream parts of the tunnel systems because of the hydraulic pressures elevated above background values and long residence time of combined sewer flow in those areas. Elevated values of the analytes emplaced during intermittent migration of combined sewer flow into the Silurian aquifer decrease through time as water from the aquifer drains back into the tunnels in response to typical hydraulic conditions. Of the analytes sampled, fecal coliform provides the clearest indication of the location and timing of combined sewer flow into the Silurian aquifer surrounding the tunnel system.

Illinois↗

USGS2016

Application of hydrogeology and groundwater-age estimates to assess the travel time of groundwater at the site of a landfill to the Mahomet Aquifer, near Clinton, Illinois

The U.S. Geological Survey used interpretations of hydrogeologic conditions and tritium-based groundwater age estimates to assess the travel time of groundwater at a landfill site near Clinton, Illinois (the “Clinton site”) where a chemical waste unit (CWU) was proposed to be within the Clinton landfill unit #3 (CLU#3). Glacial deposits beneath the CWU consist predominantly of low-permeability silt- and clay-rich till interspersed with thin (typically less than 2 feet in thickness) layers of more permeable deposits, including the Upper and Lower Radnor Till Sands and the Organic Soil unit. These glacial deposits are about 170 feet thick and overlie the Mahomet Sand Member of the Banner Formation. The Mahomet aquifer is composed of the Mahomet Sand Member and is used for water supply in much of east-central Illinois. Eight tritium analyses of water from seven wells were used to evaluate the overall age of recharge to aquifers beneath the Clinton site. Groundwater samples were collected from six monitoring wells on or adjacent to the CLU#3 that were open to glacial deposits above the Mahomet aquifer (the upper and lower parts of the Radnor Till Member and the Organic Soil unit) and one proximal production well (approximately 0.5 miles from the CLU#3) that is screened in the Mahomet aquifer. The tritium-based age estimates were computed with a simplifying, piston-flow assumption: that groundwater moves in discrete packets to the sampled interval by advection, without hydrodynamic dispersion or mixing. Tritium concentrations indicate a recharge age of at least 59 years (pre-1953 recharge) for water sampled from deposits below the upper part of the Radnor Till Member at the CLU#3, with older water expected at progressively greater depth in the tills. The largest tritium concentration from a well sampled by this study (well G53S; 0.32 ± 0.10 tritium units) was in groundwater from a sand deposit in the upper part of the Radnor Till Member; the shallowest permeable unit sampled by this study. That result indicated that nearly all groundwater sampled from well G53S entered the aquifer as recharge before 1953. Tritium was detected in a trace concentration in one sample from a second monitoring well open to the upper part of the Radnor Till Member (well G07S; 0.11 ± 0.09 tritium units), and not detected in samples collected from two monitoring wells open to a sand deposit in the lower part of the Radnor Till Member, from two samples collected from two monitoring wells open to the Organic Soil unit, and in two samples collected from a production well screened in the middle of the Mahomet aquifer (a groundwater sample and a sequential replicate sample). The lack of tritium in five of the six groundwater samples collected from the shallow permeable units beneath CLU#3 site and the two samples from the one Mahomet aquifer well indicates an absence of post-1952 recharge. Groundwater-flow paths that could contribute post-1952 recharge to the lower part of the Radnor Till Member, the Organic Soil unit, or the Mahomet aquifer at the CLU#3 are not indicated by these data. Hypothetical two-part mixtures of tritium-dead, pre-1953 recharge water and decay-corrected tritium concentrations in post-1952 recharge were computed and compared with tritium analyses in groundwater sampled from monitoring wells at the CLU#3 site to evaluate whether tritium concentrations in groundwater could be represented by mixtures involving some post-1952 recharge. Results from the hypothetical two-part mixtures indicate that groundwater from monitoring well (G53S) was predominantly composed of pre-1953 recharge and that if present, younger, post-1955 recharge, contributed less than 2.5 percent to that sample. The hypothetical two-part mixing results also indicated that very small amounts of post-1952 recharge composing less than about 2.5 percent of the sample volume could not be distinguished in groundwater samples with tritium concentrations less than about 0.15 TU. The piston-flow based age of recharge determined from the tritium concentration in the groundwater sample from monitoring well G53S yielded an estimated maximum vertical velocity from the land surface to the upper part of the Radnor Till Member of 0.85 feet per year or less. This velocity, ifassumed to apply to the remaining glacial till deposits above the Mahomet aquifer, indicates that recharge flows through the 170 feet of glacial deposits between the base of the proposed chemical waste unit and the top of the Mahomet aquifer in a minimum of 200 years or longer. Analysis of hydraulic data from the site, constrained by a tritium-age based maximum groundwater velocity estimate, computed minimum estimates of effective porosity that range from about 0.021 to 0.024 for the predominantly till deposits above the Mahomet aquifer. Estimated rates of transport of recharge from land surface to the Mahomet aquifer for the CLU#3 site computed using the Darcy velocity equation with site-specific data were about 260 years or longer. The Darcy velocity-based estimates were computed using values that were based on tritium data, estimates of vertical velocity and effective porosity and available site-specific data. Solution of the Darcy velocity equation indicated that maximum vertical groundwater velocities through the deposits above the aquifer were 0.41 or 0.61 feet per year, depending on the site-specific values of vertical hydraulic conductivity (laboratory triaxial test values) and effective porosity used for the computation. The resulting calculated minimum travel times for groundwater to flow from the top of the Berry Clay Member (at the base of the proposed chemical waste unit) to the top of the Mahomet aquifer ranged from about 260 to 370 years, depending on the velocity value used in the calculation. In comparison, plausible travel times calculated using vertical hydraulic conductivity values from a previously published regional groundwater flow model were either slightly less than or longer than those calculated using site data and ranged from 230 to 580 years. Tritium data from 1996 to 2011 USGS regional sampling of groundwater from domestic wells in the confined part of the Mahomet aquifer—which are 2.5 to about 40 miles from the Clinton site—were compared with site-specific data from a production well at the Clinton site. Tritium-based groundwater-age estimates indicated predominantly pre- 1953 recharge dates for USGS and other prior regional samples of groundwater from domestic wells in the Mahomet aquifer. These results agreed with the tritium-based, pre-1953 recharge age estimated for a groundwater sample and a sequential replicate sample from a production well in the confined part of the Mahomet aquifer beneath the Clinton site. The regional tritium-based groundwater age estimates also were compared with pesticide detections in samples from distal domestic wells in the USGS regional network that are about 2.5 to 40 miles from the Clinton site to identify whether very small amounts of post-1952 recharge have in places reached confined parts of the Mahomet aquifer at locations other than the Clinton site in an approximately 2,000 square mile area of the Mahomet aquifer. Very small amounts of post-1952 recharge were defined in this analysis as less than about 2.5 percent of the total recharge contributing to a groundwater sample, based on results from the two-part mixing analysis of tritium data from the Clinton site. Pesticide-based groundwater-age estimates based on 22 detections of pesticides (13 of these detections were estimated concentrations), including atrazine, deethylatrazine (2-Chloro-4-isopropylamino-6-amino- s-triazine), cyanazine, diazinon, metolachlor, molinate, prometon, and trifluralin in groundwater samples from 10 domestic wells 2.5 to about 40 miles distant from the Clinton site indicate that very small amounts of post-1956 to post-1992 recharge can in places reach the confined part of the Mahomet aquifer in other parts of central Illinois. The relative lack of tritium in these samples indicate that the amounts of post-1956 to post-1992 recharge contributing to the 10 domestic wells were a very small part of the overall older groundwater sampled from those wells. The flow process by which very small amounts of pesticide-bearing groundwater reached the screened intervals of the 10 domestic wells could not be distinguished between well-integrity related infiltration and natural hydrogeologic features. Potential explanations include: (1) infiltration through man-made avenues in or along the well, (2) flow of very small amounts of post-1956 to post-1992 recharge through sparsely distributed natural permeable aspects of the glacial till and diluted by mixing with older groundwater, or (3) a combination of both processes. Presuming the domestic wells sampled by the USGS in 1996–2011 in the regional study of the confined part of the Mahomet aquifer are adequately sealed and produce groundwater that is representative of aquifer conditions, the regional tritium and pesticide-based groundwater-age results indicate substantial heterogeneity in the glacial stratigraphy above the Mahomet aquifer. The pesticide-based groundwater-age estimates from the domestic wells distant from the Clinton site also indicate that parts of the Mahomet aquifer with the pesticide detections can be susceptible to contaminant sources at the land surface. The regional pesticide and tritium results from the domestic wells further indicate that a potential exists for possible contaminants from land surface to be transported through the glacial drift deposits that confine the Mahomet aquifer in other parts of central Illinois at faster rates than those computed for recharge at the Clinton site, including CLU#3. This analysis indicates the potential value of sub-microgram-per-liter level concentrations of land-use derived indicators of modern recharge to indicate the presence of very small amounts of modern, post-1952 age recharge in overall older, pre-1953 age groundwater.

Illinois↗

USGS2011

Diel cycles in dissolved barium, lead, iron, vanadium, and nitrite in a stream draining a former zinc smelter site near Hegeler, Illinois

Diel variations in the concentrations of a number of constituents have the potential to substantially affect the appropriate sampling regimen in acidic streams. Samples taken once during the course of the day cannot adequately reflect diel variations in water quality and may result in an inaccurate understanding of biogeochemical processes, ecological conditions, and of the threat posed by the water to human health and the associated wildlife. Surface water and groundwater affected by acid drainage were sampled every 60 to 90 min over a 48-hour period at a former zinc smelter known as the Hegeler Zinc Superfund Site, near Hegeler, Illinois. Diel variations related to water quality in the aquifer were not observed in groundwater. Diel variations were observed in the temperature, pH, and concentration of dissolved oxygen, nitrite, barium, iron, lead, vanadium, and possibly uranium in surface water. Temperature, dissolved oxygen, nitrite, barium, lead, and uranium generally attained maximum values during the afternoon and minimum values during the night. Iron, vanadium, and pH generally attained minimum values during the afternoon and maximum values during the night. Concentrations of dissolved oxygen were affected by the intensity of photosynthetic activity and respiration, which are dependent upon insolation. Nitrite, an intermediary in many nitrogen reactions, may have been formed by the oxidation of ammonium by dissolved oxygen and converted to other nitrogen species as part of the decomposition of organic matter. The timing of the pH cycles was distinctly different from the cycles found in Midwestern alkaline streams and likely was the result of the photoreduction of Fe 3+ to Fe 2+ and variations in the intensity of precipitation of hydrous ferric oxide minerals. Diel cycles of iron and vanadium also were primarily the result of variations in the intensity of precipitation of hydrous ferric oxide minerals. The diel variation in the concentrations of lead, uranium, and barium may have been affected by competition with Fe + 2 for sorption sites on hydrous ferric oxide minerals.

Illinois↗

USGS2010

Hydrology, water quality, and causes of changes in vegetation in the vicinity of the Spring Bluff Nature Preserve, Lake County, Illinois, May 2007–August 2008

Agriculture and urbanization have altered the hydrology and water quality of the coastal wetland complex along the shore of Lake Michigan at the Spring Bluff Nature Preserve and Illinois Beach State Park in northeastern Lake County, Ill., and the adjacent Chiwaukee Prairie State Natural Area in southeastern Wisconsin. Culverts, roads, ditches, and berms installed within the wetland complex have altered the natural directions of surface-water flow and likely have increased the natural hydroperiod in the Spring Bluff Nature Preserve and decreased it in the northern part of the Illinois Beach State Park. Relative to presettlement conditions, surface-water runoff into the wetlands likely is greater in quantity and higher in concentrations of several constituents, including chloride, nitrate, phosphorous, and suspended sediment. These constituent concentrations are affected by a variety of factors, including the amount of agricultural and urban land use in the watersheds. Hydrologic, chemical, and biologic processes within the wetland communities reduce the concentrations of these constituents in surface water before the water discharges to Lake Michigan by as much as 75 percent for chloride, 85 percent for nitrate, 66 percent for phosphorous, and more than an order of magnitude for suspended sediment. However, concentrations of phosphorous and suspended sediment in surface water increased within parts of the wetland complex. Given these changes, the floristic quality of these wetlands has been altered from the historic condition. Specifically, Typha spp. and Phragmites australis occur in greater numbers and over a larger area than in the past. The spread of Typha spp. and Phragmites australis appears to be enhanced by anthropogenic alterations within the wetland complex, such as increased water levels and duration of inundation and, possibly, increases in the total concentration of dissolved constituents in water.

Illinois↗

USGS2009

Diel Sampling of Groundwater and Surface Water for Trace Elements and Select Water-Quality Constituents at a Former Zinc Smelter Site near Hegeler, Illinois, August 1-3, 2007

Surface water can exhibit substantial diel variations in the concentration of a number of constituents. Sampling regimens that do not characterize diel variations in water quality can result in an inaccurate understanding of site conditions and of the threat posed by the site to human health and the environment. Surface- and groundwater affected by acid drainage were sampled every 60 to 90 minutes over a 48-hour period at a former zinc smelter known as the Hegeler Zinc Superfund Site, in Hegeler, Ill. Groundwater-quality data from a well at the site indicate stable, low pH, weakly oxidizing geochemical conditions in the aquifer. With the exceptions of temperature and pH, no constituents exhibited diel variations in groundwater. Variations in temperature and pH likely were not representative of conditions in the aquifer. Surface water was sampled at a site on Grape Creek. Diel variations were observed in temperature, dissolved oxygen, pH, and specific conductance, and in the concentrations of nitrite, barium, iron, lead, vanadium, and possibly uranium. Concentrations during the diel cycles varied by about an order of magnitude for nitrite and varied by about a factor of two for barium, iron, lead, vanadium, and uranium. Temperature, dissolved oxygen, specific conductance, nitrite, barium, lead, and uranium generally reached maximum values during the afternoon and minimum values during the night. Iron, vanadium, and pH generally reached minimum values during the afternoon and maximum values during the night. These variations would need to be accounted for during sampling of surface-water quality in similar hydrologic settings. The temperature variations in surface water were affected by variations in air temperature. Concentrations of dissolved oxygen were affected by variations in the intensity of photosynthetic activity and respiration. Nitrite likely was formed by the oxidation of ammonium by dissolved oxygen and degraded by its anaerobic oxidation by ammonium or as part of the decomposition of organic matter. Variations in pH were affected by the photoreduction of Fe3+ to Fe2+ and the precipitation of iron oxyhydroxides. Diel variations in concentrations of iron and vanadium were likely caused by variations in the dissolution and precipitation of iron oxyhydroxides, oxyhydroxysulfates, and hydrous sulfates, which may have been affected by in the intensity of insolation, iron photoreduction, and the concentration of dissolved oxygen. The concentrations of lead, uranium, and perhaps barium in Grape Creek may have been affected by competition for sorption sites on iron oxyhydroxides. Competition for sorption sites was likely affected by variations in pH and the concentration of Fe2+. Constituent concentrations likely also were affected by precipitation and dissolution of minerals that are sensitive to changes in pH, temperature, oxidation-reduction conditions, and biologic activity. The chemical and biologic processes that resulted in the diel variations observed in Grape Creek occurred within the surface-water column or in the underlying sediments.

Scientific Investigations Report↗

USGS2007

Hydrogeology of the Piney Point-Nanjemoy, Aquia, and Upper Patapsco aquifers, Naval Air Station Patuxent River and Webster Outlying Field, St. Marys County, Maryland, 2000–06

Recent and projected population growth in southern Maryland continues to bring ground-water-quality and quantity issues to the forefront. Lithologic, borehole geophysical, water-level, and water-use data were compiled and interpreted to revise understanding of the hydrogeologic framework of the Piney Point-Nanjemoy, Aquia, and Upper Patapsco aquifers in southern Maryland, with emphasis on the Naval Air Station Patuxent River and Webster Outlying Field. Understanding of the hydrogeologic framework for the Upper Patapsco aquifer also has been revised based on the results of aquifer testing and water-quality sampling of two wells. The Piney Point-Nanjemoy aquifer is 50 to 70 feet thick, with a top altitude of 213 to 260 feet below the North American Vertical Datum of 1988 and a hydraulic conductivity of 2 feet per day at Naval Air Station Patuxent River and Webster Outlying Field. Ground-water withdrawals from the Piney Point-Nanjemoy aquifer have been minimal since 1999 and water levels in the aquifer have not changed substantially since the 1950s. An overall decline of about 2.5 feet has been observed since 1997, however. The Aquia aquifer is 100 to 145 feet thick, with a top altitude of approximately 450 feet below the North American Vertical Datum of 1988 and a hydraulic conductivity of 6 to 10 feet per day at Naval Air Station Patuxent River. The Aquia aquifer is approximately 50 feet thick, with a top altitude of 470 feet below sea level and a hydraulic conductivity of 6 to 10 feet per day at Webster Outlying Field. Water levels in the Aquia aquifer declined in response to increased withdrawals from the aquifer from the early 1940s through about 2000 at Naval Air Station Patuxent River and Webster Outlying Field, but have been generally stable from about 1999 through April 2006. The Upper Patapsco aquifer at the Naval Air Station Patuxent River and Webster Outlying Field consists of layers of sand interbedded with layers of clay that total over 200 feet in thickness. The top of the aquifer near Naval Air Station Patuxent River and Webster Outlying Field ranges from approximately 620 to 680 feet below the North American Vertical Datum of 1988. The potentiometric surface of the Upper Patapsco aquifer near Naval Air Station Patuxent River and Webster Outlying Field has been declining at a rate of about 2 feet per year for the past several years. Aquifer testing indicates the transmissivity of the aquifer is about 2,100 to 3,900 feet squared per day. Water samples collected from the Upper Patapsco aquifer at Naval Air Station Patuxent River and Webster Outlying Field in 2000 and 2001 met all Federal drinking-water standards.

Scientific Investigations Report↗

USGS2007

Evaluation of ground-water and boron sources by use of boron stable-isotope ratios, tritium, and selected water-chemistry constituents near Beverly Shores, northwestern Indiana, 2004

Concentrations of boron greater than the U.S. Environmental Protection Agency (USEPA) 900 μg/L removal action level (RAL) standard were detected in water sampled by the USEPA in 2004 from three domestic wells near Beverly Shores, Indiana. The RAL regulates only human-affected concentrations of a constituent. A lack of well logs and screened depth information precluded identification of whether water from sampled wells, and their boron sources, were from human-affected or natural sources in the surficial aquifer, or associated with a previously defined natural, confined aquifer source of boron from the subtill or basal sand aquifers. A geochemically-based classification of the source of boron in ground water could potentially determine the similarity of boron to known sources or mixtures between known sources, or classify whether the relative age of the ground water predated the potential sources of contamination. The U.S. Geological Survey (USGS), in cooperation with the USEPA, investigated the use of a geochemical method that applied boron stable isotopes, and concentrations of boron, tritium, and other constituents to distinguish between natural and human-affected sources of boron in ground water and thereby determine if the RAL was applicable to the situation. Boron stable-isotope ratios and concentrations of boron in 17 ground-water samples and tritium concentrations in 9 ground-water samples collected in 2004 were used to identify geochemical differences between potential sources of boron in ground water near Beverly Shores, Indiana. Boron and δ 11 B analyses for this investigation were made on unacidified samples to assure consistency of the result with unacidified analyses of δ 11 B values from other investigations. Potential sources of boron included surficial-aquifer water affected by coal-combustion products (CCP) or domestic-wastewater, upward discharge of ground water from confined aquifers, and unaffected water from the surficial aquifer that was distant from human-affected boron sources. Boron concentrations in potential ground-water sources of boron were largest (15,700 to 24,400 μg/L) in samples of CCP-affected surficial aquifer water from four wells at a CCP landfill and smallest (27 to 63 μg/L) in three wells in the surficial aquifer that were distant from human-affected boron sources. Boron concentrations in water from the basal sand aquifer ranged from 656 μg/L to 1,800 μg/L. Boron concentrations in water from three domestic-wastewater-affected surficial aquifer wells ranged from 84 to 387 μg/L. Among the representative ground-water samples, boron concentrations from all four samples of CCP-affected surficial aquifer water and four of five samples of water from the basal sand aquifer had concentrations greater than the RAL. A comparison of boron concentrations in acid-preserved and unacidified samples indicated that boron concentrations reported for this investigation may be from about 11 to 16 percent less than would be reported in a standard analysis of an acidified sample. The stable isotope boron-11 was most enriched in comparison to boron-10 in ground water from a confined aquifer, the basal sand aquifer (δ 11 B, 24.6 to 34.0 per mil, five samples); it was most depleted in CCP-affected water from the surficial aquifer (δ 11 B, 0.1 to 6.6 per mil, four samples). Domestic-wastewater-affected water from the surficial aquifer (δ 11 B, 8.7 to 11.7 per mil, four samples) was enriched in boron-11, in comparison to individual samples of a borax detergent additive and a detergent with perborate bleach; it was intermediate in composition between basal sand aquifer water and CCP-affected water from the surficial aquifer. The similarity between a ground-water sample from the surficial aquifer and a hypothetical mixture of unaffected surficial aquifer and basal sand aquifer waters indicates the potential for long-term upward discharge of ground water into the surficial aquifer from one or more confined aquifers. Estimated δ 11 B values for acidified samples were depleted by 1.9 to 2.8 per mil in comparison to unacidified samples from the four wells sampled; those differences were small in comparison to the differences between δ 11 B values of representative sources of boron in ground water. Tritium concentrations ranged from 7.0 to 10.3 tritium units in six samples from the surficial aquifer and were less than 0.8 tritium units in three samples from the basal sand aquifer. Water from wells in the surficial aquifer represents predominantly modern, post-1972 recharge and sources of boron and other constituents. Water from the basal sand aquifer is associated with pre-1952 recharge from sources not affected by local boron inputs. Ground water from six wells (five domestic wells and one public-supply well) where the ground-water source was unknown had boron concentrations, boron isotope ratios, and tritium concentrations similar to water from the basal sand aquifer. Boron concentrations greater than the RAL were found in water from four of these six wells. The boron isotope and tritium data from these four wells indicate a natural source of boron in ground water; therefore, the RAL does not apply to boron concentrations in water from these wells. Water samples from two domestic wells where the ground-water source was unknown had boron concentrations less than the RAL and boron isotope ratios and tritium concentrations that were similar to domestic-wastewater-affected water from the surficial aquifer. The boron isotope ratio for a sample from one domestic well was similar to that of CCP-affected water from the surficial aquifer and detergent compositions; the boron concentration of that sample was less than the RAL. The classifications of differences among representative sources of boron in ground water and water samples from wells where the ground-water source was unknown generally agreed with distinctions based on strontium-87/strontium-86 ratios and concentrations of strontium, chloride, nitrate, and ammonia. This application of boron concentrations, boron isotope ratios, and tritium concentrations to classify differences in relation to potential sources of boron in ground water was able to distinguish between boron from natural sources and from human-affected sources that are subject to regulation.

Indiana↗

USGS2005

Surface-Water and Ground-Water Resources of Kendall County, Illinois

Water-supply needs in Kendall County, in northern Illinois, are met exclusively from ground water derived from glacial drift aquifers and bedrock aquifers open to Silurian, Ordovician, and Cambrian System units. As a result of population growth in Kendall County and the surrounding area, water use has increased from about 1.2 million gallons per day in 1957 to more than 5 million gallons per day in 2000. The purpose of this report is to characterize the surface-water and ground-water resources of Kendall County. The report presents a compilation of available information on geology, surface-water and ground-water hydrology, water quality, and water use. The Fox River is the primary surface-water body in Kendall County and is used for both wastewater disposal and as a drinking-water supply upstream of the county. Water from the Fox River requires pretreatment for use as drinking water, but the river is a potentially viable additional source of water for the county. Glacial drift aquifers capable of yielding sufficient water for municipal supply are expected to be present in northern Kendall County, along the Fox River, and in the Newark Valley and its tributaries. Glacial drift aquifers capable of yielding sufficient water for residential supply are present in most of the county, with the exception of the southeastern portion. Volatile organic compounds and select trace metals and pesticides have been detected at low concentrations in glacial drift aquifers near waste-disposal sites. Agricultural-related constituents have been detected infrequently in glacial drift aquifers near agricultural areas. However, on the basis of the available data, widespread, consistent problems with water quality are not apparent in these aquifers. These aquifers are a viable source for additional water supply, but would require further characterization prior to full development. The shallow bedrock aquifer is composed of the sandstone units of the Ancell Group, the Prairie du Chien Group, the Galena-Platteville dolomite, the Maquoketa Group, and the Silurian dolomite where these units are at the bedrock surface. The availability of water from the shallow bedrock aquifer depends primarily on the geologic unit utilized. The Silurian dolomite, Galena-Platteville dolomite, and Ancell Group can yield sufficient water for residential and municipal supply in at least some parts of the county. The Cambrian-Ordovician aquifer system is composed of the most widespread, productive aquifers in northern Illinois and is used for water supply by a number of municipalities and industrial facilities. Water levels in the aquifer system have declined by as much as 600 feet in Kendall County and the aquifer frequently contains concentrations of radium above established health guidelines.

Scientific Investigations Report↗

USGS2004

A cross-site comparison of methods used for hydrogeologic characterization of the Galena-Platteville aquifer in Illinois and Wisconsin, with examples from selected Superfund sites

The effectiveness of 28 methods used to characterize the fractured Galena-Platteville aquifer at eight sites in northern Illinois and Wisconsin is evaluated. Analysis of government databases, previous investigations, topographic maps, aerial photographs, and outcrops was essential to understanding the hydrogeology in the area to be investigated. The effectiveness of surface-geophysical methods depended on site geology. Lithologic logging provided essential information for site characterization. Cores were used for stratigraphy and geotechnical analysis. Natural-gamma logging helped identify the effect of lithology on the location of secondary- permeability features. Caliper logging identified large secondary-permeability features. Neutron logs identified trends in matrix porosity. Acoustic-televiewer logs identified numerous secondary-permeability features and their orientation. Borehole-camera logs also identified a number of secondary-permeability features. Borehole ground-penetrating radar identified lithologic and secondary-permeability features. However, the accuracy and completeness of this method is uncertain. Single-point-resistance, density, and normal resistivity logs were of limited use. Water-level and water-quality data identified flow directions and indicated the horizontal and vertical distribution of aquifer permeability and the depth of the permeable features. Temperature, spontaneous potential, and fluid-resistivity logging identified few secondary-permeability features at some sites and several features at others. Flowmeter logging was the most effective geophysical method for characterizing secondary-permeability features. Aquifer tests provided insight into the permeability distribution, identified hydraulically interconnected features, the presence of heterogeneity and anisotropy, and determined effective porosity. Aquifer heterogeneity prevented calculation of accurate hydraulic properties from some tests. Different methods, such as flowmeter logging and slug testing, occasionally produced different interpretations. Aquifer characterization improved with an increase in the number of data points, the period of data collection, and the number of methods used.

Scientific Investigations Report↗

USGS2003

Concentrations of polynuclear aromatic hydrocarbons and inorganic constituents in ambient surface soils, Chicago, Illinois: 2001-02

Polynuclear aromatic hydrocarbon (PAH) compounds are ubiquitous in ambient surface soils in the city of Chicago, Illinois. PAH concentrations in samples collected in June 2001 and January 2002 were typically in the following order from highest to lowest: fluoranthene, pyrene, benzo(b)fluoranthene, phenanthrene, benzo(a)pyrene, chrysene, benzo(a)anthracene, benzo(k)fluoranthene, indeno(1,2,3-cd)pyrene, benzo(g,h,i)perylene, dibenzo(a,h)anthracene, and anthracene. Naphthalene, acenaphthene, acenaphthylene, and fluorene were consistently at the lowest concentrations in each sample. Concentrations of the PAH compounds showed variable correlation. Concentrations of PAH compounds with higher molecular weights typically show a higher degree of correlation with other PAH compounds of higher molecular weight, whereas PAH compounds with lower molecular weights tended to show a lower degree of correlation with all other PAH compounds. These differences indicate that high and low molecular-weight PAHs behave differentl y once released into the environment. Concentrations of individual PAH compounds in soils typically varied by at least three orders of magnitude across the city and varied by more than an order of magnitude over a distance of about 1,000 feet. Concentrations of a given PAH in ambient surface soils are affected by a variety of site-specific factors, and may be affected by proximity to industrial areas. Concentrations of a given PAH in ambient surface soils did not appear to be affected the organic carbon content of the soil, proximity to non-industrial land use, or proximity to a roadway. The concentration of the different PAH compounds in ambient surface soils appears to be affected by the propensity for the PAH compound to be in the vapor or particulate phase in the atmosphere. Lower molecular-weight PAH compounds, which are primarily in the vapor phase in the atmosphere, were detected in lower concentrations in the surface soils. Higher molecular-weight PAH compounds, which are present primarily in the particulate phase in the atmosphere, tended to be in higher concentrations in the surface soils. The apparent effect of the PAH phase in the atmosphere on the concentration of a PAH in ambient surface soils indicates that atmospheric settling of particulate matter is an important source of the PAH compounds in ambient surface soils in Chicago. The distribution of PAH compounds within the city was complex. Comparatively high concentrations were detected near Lake Michigan in the northern part of the city, in much of the western part of the city, and in isolated areas in the southern part of the city. Concentrations were lower in much of the northwestern, south-central, southwestern, and far southern parts of the city. The arithmetic mean concentration of arsenic, mercury, calcium, magnesium, phosphorus, copper, molybdenum, zinc, and selenium was from 2 to 6 times higher in ambient surface soils in the city of Chicago than in soils from surrounding agricultural areas. The arithmetic mean concentration of lead in Chicago soils was about 20 times higher. Concentrations of calcium and magnesium above those of surrounding agricultural areas appear to be related to the effects of dolomite bedrock on the chemical composition of the soil. Elevated concentrations of the remaining elements listed above indicate a potential anthropogenic source(s) of these elements in Chicago soils.

Illinois↗

USGS2002

Estimated water withdrawals, water use, and water consumption in Illinois, Indiana, Iowa, Kentucky, Michigan, Missouri, and Wisconsin, 1950-95

From 1950 through 1995, the U.S. Geological Survey tabulated water withdrawals throughout the United States, including the northcentral States of Illinois, Indiana, Iowa, Kentucky, Michigan, Missouri, and Wisconsin. During this period, total water withdrawals increased in each of the north-central States by at least a factor of two. Illinois led the north-central States in total withdrawals, withdrawals from surface water and, typically, withdrawals from ground water. Per capita withdrawals were largest in Indiana or Illinois, however, the disparity in per capita withdrawals in the north-central States decreased from 1950 through 1995. Surface water was the source of 75 to 95 percent of all water withdrawals in the north-central States and consistently accounted for over 90 percent of total withdrawals in Illinois. From 1950 through 1995, the magnitude of increase in withdrawals from surface water was lower in Illinois than in most of the other north-central States, even though surface-water withdrawals in Illinois increased from about 9,000 to 19,000 million gallons per day. Total water withdrawals from ground water in Illinois have decreased by about 150 million gallons per day since 1975. From 1950 through 1995, from 68 to 86 percent of the total water withdrawals in Illinois were for generation of thermoelectric power; this percentage is higher than for the other north-central States and has increased since 1970. Approximately 12 percent of water withdrawals in Illinois are for municipal water supply, which was consistent with the other north-central States. Ten percent or less of the water withdrawn in the north-central States is estimated to have been consumed.

Water-Resources Investigations Report↗