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USGS1987

Source of salts in the Waianae part of the Pearl Harbor aquifer near Barbers Point water tunnel, Oahu, Hawaii

The salinity of the water supply of Barbers Point Naval Air Station has increased markedly since 1983. The Naval Air Station obtains its water, about 3 million gal/day, from Barbers Point shaft, a water shaft that taps the Waianae part of the Pearl Harbor aquifer underlying the dry, southeastern flank of the Waianae mountains on the island on Oahu, Hawaii. From 1983 to 1985 the chloride concentration of the water, increased from 220 to 250 mg/L and has remained near that level through 1986. The EPA has established 250 mg/L as the maximum recommended chloride concentration in drinking water because above that level many people can taste the salt. The high chloride concentration in shallow groundwater at all wells in the area indicates that most of the salts in the freshwater lens are contributed by rainfall, sea spray, and irrigation return water. At Barbers Point shaft, pumping may draw a small amount of saltwater from the transition zone and increase the chloride concentration in the pumped water by about 20 mg/L. Salinity of the lens decreases progressively inland in response to recharge from relatively fresher water and in response to an increasing lens thickness with increasing distance from the shoreline. The increase, in 1983, in the chloride concentration of water at the shaft was most probably the result of saltier recharge water reaching the water table, and not the result of increased mixing of underlying saltwater with the freshwater. The chloride concentration of the recharge water has probably increased because, in 1980, the drip method of irrigation began to replace the furrow method on sugarcane fields near the shaft. A mixing-cell model was used to estimate the effect of drip irrigation on the chloride concentration of the groundwater in the vicinity of Barbers Point shaft. The model predicted an increase in chloride concentration of about 50 mg/L. The observed increase was about 30 mg/L and the chloride concentration is presently stable at 245 to 250 mg/L; hence, the chloride concentration is not expected to increase significantly more. (Lantz-PTT)

Water-Resources Investigations Report↗

USGS2019

Potential interaction of groundwater and surface water including autonomous underwater vehicle reconnaissance at Nolin River Lake, Kentucky, 2016

The U.S. Geological Survey collaborated with the U.S. Army Corps of Engineers, Louisville District, on a synoptic study of water quality at Nolin River Lake during August 2016. The purpose of the study was to develop a better understanding of the potential for interaction between groundwater and surface water at Nolin River Lake, Kentucky. Groundwater can have properties that are measurably different from those in adjacent surface water, and inflows and outflows can be an important component of water quality and quantity. An improved understanding of potential interaction of groundwater and surface water at Nolin River Lake may be used to refine lake-management strategies. This study (1) compiled and interpreted existing information to characterize the hydrogeological setting and implications for potential interaction of groundwater and surface water in the Nolin River Lake watershed; (2) collected transects of onsite water-quality parameters using an autonomous underwater vehicle (AUV) in areas with potential for interaction of groundwater and surface water, including five sites on Nolin River Lake and one site on the Nolin River; and (3) collected discrete water-quality and phytoplankton community data at the same six sites. A review of existing hydrogeologic information did not indicate the presence of karst features adjacent to or beneath Nolin River Lake that would facilitate groundwater interaction with the reservoir. Observations leading to this conclusion include (1) limestone that is adjacent to the shoreline and perhaps beneath the lake, is overlain with siliciclastic rocks and fine-grained sediment that inhibits infiltration and development of karst features that encourage rapid groundwater flow; (2) the geologic deposits surrounding the reservoir are described as having limited or no potential for development of karst features, some exceptions may exist in tributary valleys; (3) very few karst features were mapped within 1 mile of the reservoir or in the area currently occupied by the reservoir; and (4) faults that intersect the reservoir but may not possess hydraulic properties that cause the faults to be conduits for groundwater flow. Groundwater interaction with reservoir tributaries is likely more common in areas of the watershed upstream from Nolin River Lake where karst hydrogeology is prevalent. Results of water-quality surveys using an AUV from August 15 to 19, 2016, did not identify areas of anomalous values that might indicate groundwater inflows through preferential flow zones. Spatial distributions of water-quality parameters were generally uniform within each constant-depth layer. The constant-depth layers were selected to be above, within, and below the thermocline and ranged from the water surface to 25 feet. Surveys near the bottom of the reservoir that might have been more sensitive to groundwater inflows were not done because presurvey data were not available to indicate locations of obstacles that could ensnare the AUV. Water-quality data collected with the AUV did identify water-quality anomalies where stream tributaries were discharging to the reservoir. The discrete water-quality samples indicated uniformity among the five reservoir sites. The riverine site that is immediately upstream from Nolin River Lake, however, had some unique water-quality characteristics relative to sites on the reservoir. The highest concentrations of nitrate plus nitrite as nitrogen (0.145 milligrams per liter [mg/L]), total phosphorous (0.07 mg/L), chlorophyll a (36.1 micrograms per liter), and pheophytin a (10.2 micrograms per liter) were measured at the Nolin River Lake riverine site (site 2NRR20034). The concentrations of nutrients and chlorophyll a at the riverine site did exceed the 25th percentile of median concentrations measured by the U.S. Environmental Protection Agency (EPA) at other lakes and reservoirs in EPA level IV ecoregion 71a. Concentrations of most nutrients and chlorophyll a at the five reservoir sites also exceeded the 25th percentile of median concentrations in EPA level IV ecoregion 72h. The exception was the concentrations of total phosphorus as phosphorus at the reservoir sites that were at or below the 25th percentile of median concentrations measured by EPA (0.03 mg/L). Concentrations of orthophosphate as phosphorus were less than the method detection limit of 0.004 mg/L at all sites. The phytoplankton community in Nolin River Lake was almost exclusively (greater than 90 percent of total phytoplankton abundance) cyanobacteria, also known as blue-green algae. A species of Cylindrospermopsis dominated the cyanobacterial community at the five reservoir sites, while Chroococcus microscopicus was most abundant at the riverine site. Cyanobacterial cell densities ranged from 10,000 to 198,067,460 cells per liter in five areas in the reservoir and from 4,800 to 73,751,253 cells per liter at the riverine site. Multiple potential sources of water to Nolin River Lake include direct precipitation, overland flow, interflow, groundwater, and surface water. Understanding the exact contribution of each of these components to the water budget at Nolin River Lake may help the U.S. Army Corps of Engineers manage the water quality, water quantity, and biological communities in the reservoir. Additional hydrogeologic and water-quality data that builds on the results of this study may refine the inferences of this study; for example, deeper AUV surveys that target the largest fault zones might further the understanding of the potential for groundwater flow through those features. A complete understanding of the reservoir hydrology, however, may require the use of scientific methods intended for water bodies as large as Nolin River Lake, such as aerial infrared photography and imagery; water mass, chemical, and isotopic balance studies; geophysical measurements; and numerical simulations.

Kentucky↗

USGS2000

Overview of the Texas Source Water Assessment Project

The 1996 Amendments to the Safe Drinking Water Act require, for the first time, that each state prepare a source water assessment for all PWS. Previously, Federal regulations focused on sampling and enforcement with emphasis on the quality of delivered water. These Amendments emphasize the importance of protecting the source water. States are required to determine the drinking-water source, the origin of contaminants monitored or the potential contaminants to be monitored, and the intrinsic susceptibility of the source water. Under the amendments to the Act, States must create SWAP Programs. The programs must include an individual source water assessment for each public water system regulated by the State. These assessments will determine whether an individual drinking water source is susceptible to contamination. During 1997?99, TNRCC and USGS staff met as subject-matter working groups to develop an approach to conducting Source Water Susceptibility Assessments (SWSA) and a draft workplan. The draft workplan was then presented to and reviewed by various stakeholder and technical advisory groups. Comments and suggestions from these groups were considered, and a final workplan was produced and presented to the EPA. After EPA approval, work formally began on the Texas SWAP Project. The project has an expected completion date of September 2002. At that time, initial SWSA of all Texas public water supplies should be complete. Ground-water supplies can be considered susceptible if a possible source of contamination (PSOC) exists in the contributing area for the public-supply well field or spring, the contaminant travel time to the well field or spring is short, and the soil zone, vadose zone, and aquifer-matrix materials are unlikely to adequately attenuate the contaminants associated with the PSOC. In addition, particular types of land use/cover within the contributing area may cause the supply to be deemed more susceptible to contamination. Finally, detection of various classes of constituents in water from wells in the vicinity of a public supply well may indicate susceptibility of the public-supply well even though there may be no identifiable PSOC or land use activity. Surface-water supplies are by nature susceptible to contamination from both point and non-point sources. The degree of susceptibility of a PWS to contamination can vary and is a function of the environmental setting, water and wastewater management practices, and land use/cover within a water supply's contributing watershed area. For example, a PWS intake downstream from extensive urban development may be more susceptible to non-point source contamination than a PWS intake downstream from a forested, relatively undeveloped watershed. Surface-water supplies are also susceptible to contamination from point sources, which may include permitted discharges, as well as accidental spills or other introduction of contaminants.

Texas↗

USGS2024

Assessment of water levels, nitrate, and arsenic in the Carson Valley Alluvial Aquifer and the development of a data visualization tool for the Carson River Basin, Nevada

Residents of Carson Valley, Douglas County, Nevada, rely on the basin-fill alluvial aquifer underlying the valley for drinking water. Since the 1980s, groundwater levels and water-quality data have been collected to monitor the status of the aquifer system and to assist in planning efforts to address current (2024) and future demand. The U.S. Geological Survey (USGS), in cooperation with Douglas County, Nevada, evaluated trends in water levels, nitrate, and arsenic concentrations from a network of monitoring and domestic wells in Carson Valley. This work also assessed the monitoring well network to determine the suitability of wells for characterizing the occurrence of arsenic in the groundwater. Monitoring of constituents, such as nitrate and arsenic concentrations, is needed to assess changes in contaminant distribution and to evaluate the effect that changing land use and groundwater pumping has on their occurrence and transport. Results of the trend analysis indicate water levels are declining ( p <0.05) in 17 of 26 selected monitoring wells (65 percent). Areas with the largest change in water levels, with more than 20 feet of declines, were within the community areas of Johnson Lane, Ruhenstroth, South Agricultural, East Valley, and Fish Springs. Variations in water levels measured in wells from the Central Agricultural, Minden, Foothill, Alpine County (one well), and Gardnerville Ranchos areas show periods of increase and decrease over time, but they also maintain long-term declining trends ( p <0.05). Increases in nitrate concentrations in groundwater samples collected from 9 out of 14 selected monitoring wells (64 percent) are statistically significant ( p <0.05) within the Ruhenstroth, Gardnerville Ranchos, East Valley, Genoa, and Johnson Lane community areas. Samples collected from a well in Indian Hills/Jacks Valley indicated a decreasing trend in nitrate concentration over time. Nitrate concentrations in samples collected from wells in East Valley, Genoa, Johnson Lane, and Indian Hills/Jack Valley were consistently low (less than 3 milligrams per liter [mg/L]) and stable. Nitrate concentrations from selected wells in Johnson Lane and Garnerville Ranchos exceeded the U.S. Environmental Protection Agency (EPA) maximum contaminant level (MCL) of 10 mg/L (as nitrogen) and have trends that are increasing over time. In 2022, a sample collected from Johnson Lane had a concentration (7.3 mg/L) below the MCL with an increasing trend over time. Temporal trend analyses for groundwater arsenic concentrations in Carson Valley could not be done because of a lack of temporal data. However, using available historical data, arsenic concentrations seem to be greater in groundwater from wells located on the eastern and northern areas of the valley than in wells located on the western or southern areas. Groundwater arsenic concentrations exceed 5 micrograms per liter (μg/L) in most samples collected from wells in Johnson Lane, Airport, Central Agricultural, and East Valley areas and in many cases exceed the U.S. Environmental Protection Agency (EPA) MCL of 10 μg/L. Data indicate that groundwater from domestic wells screened at deeper intervals are likely more vulnerable to elevated arsenic concentrations than shallower wells. A groundwater network evaluation for Carson Valley identified potential modifications in the sampling locations and frequency to better understand the effect of groundwater pumping in communities where municipal and domestic demand are greatest, potentially enhancing understanding of contaminant transport in these areas. Potential modifications to the active well network include reducing the frequency of sample collection from existing network wells (6 out of 11) that have consistently shown low and stable nitrate concentrations, adding wells in areas where data are sparse, and increasing the number of wells in areas with elevated groundwater nitrate concentrations. Including the analysis of arsenic in samples from the active groundwater monitoring well network will provide more detail on the temporal and spatial variability of arsenic concentrations. A visualization tool for the Carson River Basin was developed to provide access to discrete and near real-time hydrologic and water-quality data. The Carson River Basin Hydro Mapper (CBH; U.S. Geological Survey, 2023b) shows active and historical discrete water levels measured by the USGS and the State of Nevada Division of Water Resources, discrete groundwater nitrate and arsenic concentration data collected by the USGS, near real-time streamflow, and surface water levels for select waterbodies. The hydrologic data in the CBH provides resource managers, the public, and the scientific community with an easily accessible tool to present and communicate the most up-to-date information available about local and basin-wide water resources.

Nevada↗

USGS1986

A preliminary evaluation of the geohydrology and water quality of the Greenacres Landfill area, Spokane County, Washington

The Greenacres Landfill, located about 11 mi east of the city of Spokane, Washington, was used for the disposal of waste from 1951 to 1972. Materials in the landfill include household and industrial waste materials, and various hazardous wastes. In 1983 the landfill was designated by the U.S. EPA as a ' Superfund ' site. The purposes of this investigation were to gather, describe, and interpret all the existing data concerning the hydrology and groundwater quality of the area surrounding the landfill, and to identify any additional data needed to describe the hydrology of the area. The quantity of water flow through the landfill as a result of precipitation on the landfill and in the drainage basin above the landfill probably ranges from 21,000 to 85,000 gal/day. This water movement may be creating a leachate and transporting some of the wastes out of the landfill. The plume would encompass an area where groundwater provides most of the water used for municipal, industrial, irrigation, and domestic purposes. Water quality analyses of water from numerous wells in the area which are open to the Spokane aquifer are available, but well 25/45-16K1 is the only well where groundwater contamination was consistently apparent. This well is only 500 ft from the landfill. Contamination of water in this well was indicated by high concentrations of dissolved mineral constituents and several organic compounds, including trans-dichloroethene (115 to 392 micrograms/L). Available data are insufficient to completely interpret the groundwater flow system near this well and the source of the contamination cannot be determined conclusively. While the existing data are adequate to provide background information, more data are needed to: (1) determine the source of contamination in well 25/45-16K1; (2) determine groundwater flow in the Spokane aquifer near well 25/45-16K1; and (3) determine the extent of contamination in the Spokane aquifer. The degree of the influence of the landfill on the Spokane aquifer cannot be determined with existing data. (Author 's abstract)

Open-File Report↗

USGS2014

Groundwater-quality characteristics for the Wyoming Groundwater-Quality Monitoring Network, November 2009 through September 2012

Groundwater samples were collected from 146 shallow (less than or equal to 500 feet deep) wells for the Wyoming Groundwater-Quality Monitoring Network, from November 2009 through September 2012. Groundwater samples were analyzed for physical characteristics, major ions and dissolved solids, trace elements, nutrients and dissolved organic carbon, uranium, stable isotopes of hydrogen and oxygen, volatile organic compounds, and coliform bacteria. Selected samples also were analyzed for gross alpha radioactivity, gross beta radioactivity, radon, tritium, gasoline range organics, diesel range organics, dissolved hydrocarbon gases (methane, ethene, and ethane), and wastewater compounds. Water-quality measurements and concentrations in some samples exceeded numerous U.S. Environmental Protection Agency (EPA) drinking water standards. Physical characteristics and constituents that exceeded EPA Maximum Contaminant Levels (MCLs) in some samples were arsenic, selenium, nitrite, nitrate, gross alpha activity, and uranium. Total coliforms and Escherichia coli in some samples exceeded EPA Maximum Contaminant Level Goals. Measurements of pH and turbidity and concentrations of chloride, sulfate, fluoride, dissolved solids, aluminum, iron, and manganese exceeded EPA Secondary Maximum Contaminant Levels in some samples. Radon concentrations in some samples exceeded the alternative MCL proposed by the EPA. Molybdenum and boron concentrations in some samples exceeded EPA Health Advisory Levels. Water-quality measurements and concentrations also exceeded numerous Wyoming Department of Environmental Quality (WDEQ) groundwater standards. Physical characteristics and constituents that exceeded WDEQ Class I domestic groundwater standards in some samples were measurements of pH and concentrations of chloride, sulfate, dissolved solids, iron, manganese, boron, selenium, nitrite, and nitrate. Measurements of pH and concentrations of chloride, sulfate, dissolved solids, aluminum, iron, manganese, boron, and selenium exceeded WDEQ Class II agriculture groundwater standards in some samples. Measurements of pH and concentrations of sulfate, dissolved solids, aluminum, boron, and selenium exceeded WDEQ Class III livestock groundwater standards in some samples. The concentrations of dissolved solids in two samples exceeded the WDEQ Class IV industry groundwater standard. Measurements of pH and concentrations of dissolved solids, aluminum, iron, manganese, and selenium exceeded WDEQ Class special (A) fish and aquatic life groundwater standards in some samples. Stable isotopes of hydrogen and oxygen measured in water samples were compared to the Global Meteoric Water Line and Local Meteoric Water Lines. Results indicated that recharge to all of the wells was derived from precipitation and that the water has undergone some fractionation, possibly because of evaporation. Concentrations of organic compounds did not exceed any State or Federal water-quality standards. Few volatile organic compounds were detected in samples, whereas gasoline range organics, diesel range organics, and methane were detected most frequently. Concentrations of wastewater compounds did not exceed any State or Federal water-quality standards. The compounds N,N-diethyl-meta-toluamide (DEET), benzophenone, and phenanthrene were detected most frequently. Bacteria samples were collected, processed, incubated, and enumerated in the field or at the U.S. Geological Survey Wyoming-Montana Water Science Center. Total coliforms and Escherichia coli were detected in some samples.

Wyoming↗

USGS2023

The blue carbon reservoirs from Maine to Long Island, NY

In response to the New England Governor and Eastern Canadian Premier 2017 Climate Change Action Plan recommendation to “manage blue carbon resources to preserve and enhance their existing carbon reservoirs,” the U.S. Environmental Protection Agency (EPA) convened a New England Blue Carbon Inventory Workgroup, comprised of a variety of federal, state, academic, and non-profit organizations to develop an inventory of blue carbon stocks from Maine to Long Island, New York. The Workgroup focused its inventory efforts on salt marshes and eelgrass meadows, leveraging existing habitat maps for geographic data. Existing data for soil organic carbon stocks were then used to calculate blue carbon stock estimates. For visual display purposes, sediment carbon heat maps were developed to highlight areas of greatest carbon accumulation. The habitat distribution and sediment carbon heat maps can be accessed on the Northeast Ocean Data Portal (www.northeastoceandata.org/eelgrass) which is a public source of expert-reviewed, interactive maps and data on the ocean ecosystem, economy, and culture of the northeastern United States and can be used to facilitate decision making by government agencies, tribal nations, businesses, non-governmental organizations (NGOs), academic institutions, and individuals. Based on available data and Workgroup calculations, the target geographic area has an estimated 218,222 acres of eelgrass meadows, salt marsh and saline Phragmites, which are estimated to provide a reservoir of 7,523,568 megagrams of blue carbon, or the equivalent to the annual carbon emissions from over 5,944,024 passenger vehicles. Due to data limitations, the carbon stock estimate represents a mere fraction of the actual quantity of accumulated carbon in these habitats. The findings from the Workgroup’s efforts and the resulting map products can help inform land and coastal management policies, fisheries management, and climate change mitigation practices. Further refinements and expansion of data are needed, including more detailed habitat maps, deeper soil core data for soil organic carbon content, and inclusion of more marine flora into calculations.

Connecticut, Maine, Massachusetts, New Hampshire, ↗

USGS2017

Hydrogeology and water quality of sand and gravel aquifers in McHenry County, Illinois, 2009–14, and comparison to conditions in 1979

Baseline conditions for the sand and gravel aquifers (groundwater) in McHenry County, Illinois, were assessed using data from a countywide network of 44 monitoring wells collecting continuous water-level data from 2009–14. In 2010, water-quality data were collected from 41 of the monitoring wells, along with five additional monitoring wells available from the U.S. Geological Survey National Water Quality Assessment Program. Periodic water-quality data were collected from 2010–14 from selected monitoring wells. The continuous water-level data were used to identify the natural and anthropogenic factors that influenced the water levels at each well. The water-level responses to natural influences such as precipitation, seasonal and annual variations, barometric pressure, and geology, and to anthropogenic influences such as pumping were used to determine (1) likely hydrogeologic setting (degree of aquifer confinement and interconnections) that, in part, are related to lithostratigraphy; and (2) areas of recharge and discharge related to vertical flow directions. Water-level trends generally were determined from the 6 years of data collection (2009–14) to infer effects of weather variability (drought) on recharge. Precipitation adds an estimated 2.4 inches per year of recharge to the aquifer. Some of this recharge is subsequently discharged to streams and some is discharged to supply wells. A few areas in the eastern half of the county had higher average recharge rates, indicating a need for adequate protection of these recharge areas. Downward vertical flow gradients in upland areas indicate that recharge to the confined aquifer units occurs near upland areas. Upward vertical flow gradients in lowland areas indicate discharge at locations of surface water and groundwater interaction (wetlands, ponds, and streams). Monitoring wells were sampled for major and minor ions, metals, and nutrients and a subset of wells was sampled for trace elements, dissolved gases, pesticides, and volatile organic compounds. The results were compared to health ‑ based and aesthetically based standards, which include the U.S. Environmental Protection Agency Maximum Contaminant Level (EPA MCL), and EPA Secondary Maximum Contaminant Levels (SMCL), as well as EPA Health-based Standards Drinking Water Advisories. Health‑based standards were exceeded for arsenic in 22 percent, sodium in 20 percent, and nitrates in 2 percent of the monitoring wells sampled. Aesthetically based standards were exceeded for total dissolved solids in 33 percent, chloride in 11 percent, iron in 85 percent, and manganese in 30 percent of the wells sampled. Many of these same constituents, such as arsenic, iron, and manganese, are naturally occurring but become elevated in areas that have anoxic, mixed, and suboxic conditions. Some areas of potential vulnerability to anthropogenic-sourced constituents in the sand and gravel aquifers were evidenced by trace amounts of volatile organic compounds and pesticides detected in water-quality samples from shallow wells (total depth less of than 46 feet below land surface) near urban settings, and by the detection of elevated major ions (chloride, sodium, magnesium, and calcium) associated, in part, with road-salt applications. Source analysis for chloride indicates mixtures of road salt, water softeners, and sewage. Continuously measured specific conductance values were used as a surrogate for continuously measured chloride concentrations in the groundwater. The estimated chloride concentrations generally were highest in spring and lowest in summer, and occasionally peak during spring melt. Overall, the range of concentrations varied depending on the local thickness and hydraulic conductivity of the aquifer. Water levels and water quality from the countywide groundwater monitoring network were compared to water levels and water-quality results in 1979 from a previous U.S. Geological Survey study. Potentiometric surface maps show areas with inferred decreases of water levels near the southern and southeastern areas of McHenry County. Significant increases were noted for total dissolved solids and specific conductance. Chloride concentrations increased as much as 521 percent in three of six wells resampled in 2015 from the previous study.

Illinois↗

USGS2021

Hydrogeologic framework, water levels, and selected contaminant concentrations at Valmont TCE Superfund Site, Luzerne County, Pennsylvania, 2020

The Valmont TCE Superfund Site, Luzerne County, Pennsylvania is underlain by fractured and folded sandstones and shales of the Pottsville and Mauch Chunk Formations, which form a fractured-rock aquifer recharged locally by precipitation. Industrial activities at the former Chromatex Plant resulted in trichloroethene (TCE) contamination of groundwater at and near the facility, which was identified in 1987 and led to listing as a Superfund site by the U.S. Environmental Protection Agency (EPA) in 1989. To address the problem of TCE concentrations in nearby residential wells that exceed the maximum contaminant level (MCL) of 5 micrograms per liter (μg/L), alternate water supplies were provided. A 2015 review of initial characterization and subsequent remediation by the EPA identified the need for an updated understanding of the complex hydrogeology and the conceptual site model. Additional contaminants present in groundwater at the site include some other volatile organic compounds (VOCs) and per- and polyfluoroalkyl substances (PFAS), predominantly consisting of perfluorooctanoic acid (PFOA) and perfluorooctanesulfonic acid (PFOS) present in concentrations that exceeded the EPA Health Advisory (HA) level of 5 nanograms per liter (ng/L) for combined PFOA and PFOS. In response to a request from the EPA in 2019, the U.S. Geological Survey (USGS) prepared cross sections and maps to provide more information about the hydrogeologic framework at and near the site and assist in improving the conceptual site model using water level and contaminant data collected by the EPA in 2020. The cross sections present lithologic correlations from available geophysical logs collected in wells from 2002 to 2014; they show alternating intervals of relatively elevated and reduced natural gamma activity that correspond to changes in lithology, with water-bearing zones and well screens commonly located at lithologic contacts, sometimes near thin coal seams. Water-bearing zones commonly are associated with fractures at or near lithologic contacts but also may be associated with fractures at or near apparent faulting. Recent (March 2020) water-level data shown on cross sections and maps indicate large downward vertical gradients and apparent radial gradients laterally to the northeast, northwest, and southwest that generally following topography. Recent (February to March 2020) data for TCE groundwater concentration shown on cross sections and maps indicate the highest TCE concentrations (greater than 3,000 μg/L and as much as 75,000 μg/L) and combined PFOA and PFOS concentrations (greater than 1,000 ng/L and up to at least 2,350 ng/L) are from shallow (less than 60 feet [ft] below land surface [bls]) and intermediate depth (60 to 100 ft bls) wells near the center of the former Chromatex Plant. TCE and PFAS (as combined PFOA and PFOS) contamination is present at greater depths, as much as 304 ft bls, as evidenced by samples collected from one well (a reconstructed former production well) near the plant, that contained concentrations of about 240 μg/L and 508 ng/L, respectively. The 2020 data also indicate that TCE and PFAS concentrations which exceed drinking-water MCL or HA levels are present in groundwater depths of less than 200 ft in an area that extends predominantly in a northeast direction from the former Chromatex Plant, and is apparently influenced by hydraulic gradients, lithology, and geologic structure.

Pennsylvania↗

USGS2022

Groundwater quality and geochemistry of the western wet gas part of the Marcellus Shale Oil and Gas Play in West Virginia

Thirty rural residential water wells in the wet gas region of the Marcellus Shale oil and gas play in northwestern West Virginia were sampled by the U.S. Geological Survey (USGS) in 2018, in cooperation with West Virginia State agencies, to analyze for a range of water-quality constituents, including major ions, trace metals, radionuclides, bacteria, and methane and other dissolved hydrocarbon gases. The groundwater-quality data collected for this study were used to assess the overall quality of groundwater in the study area in relation to public drinking-water standards. The groundwater-quality data were also evaluated with respect to geology, well depth, topographic setting, and proximity to oil and gas wells to identify possible relations to these factors. The presence of total coliform bacteria in groundwater is a potential indicator of surface contamination. The presence of Escherichia coli bacteria is indicative of fecal contamination of groundwater from either human or animal sources and may be considered an indicator of other related pathogens such as viruses. Total coliforms were detected in 26 of the 30 (87 percent) wells sampled. Eleven of the 30 (37 percent) wells sampled had detections of Escherichia coli bacteria. Sodium concentrations in 24 of 30 (80 percent) samples exceeded the U.S. Environmental Protection Agency (EPA) 20-milligram per Liter (mg/L) health-based value (HBV). Manganese, aluminum, and iron concentrations exceeded the EPA 50, 2.0, and 300 micrograms per liter (μg/L) secondary maximum contaminant level (SMCL) drinking-water standards at 14 (47 percent), 7 (23 percent), and 5 (17 percent) of the 30 wells sampled. Two of the 30 (7 percent) wells sampled had concentrations of manganese that exceeded the 300-μg/L USGS health-based screening level (HBSL). Arsenic concentrations at 7 of 30 (23 percent) wells sampled exceeded the 10-μg/L EPA maximum contaminant level (MCL) health-based drinking water standard. The EPA maximum contaminant level goal (MCLG) for arsenic is 0 μg/L and 29 of 30 wells sampled contained detectable concentrations of arsenic. None of the 30 wells sampled exceeded the U.S. Office of Surface Mining Reclamation and Enforcement (OSMRE) 28-mg/L immediate action level (IAL) for methane in groundwater and only 1 of 30 (3 percent) sites exceeded the 10-mg/L OSMRE level of concern (LOC) for methane in groundwater. Of the 28 wells sampled for radon-222 all 28 (100 percent) exceeded the EPA proposed 300-picocuries per liter (pCi/L) MCL for radon. None of the samples exceeded the 4,000-pCi/L alternate maximum contaminant level (AMCL) which is applicable to public drinking water systems that have adopted radon mitigation programs. Wilcoxon Signed Rank Tests indicated statistically significant differences at a 95 percent confidence interval (p less than 0.05) in radium-226, barium, and ethane groundwater concentrations with respect to the density of oil and gas wells present within a 500-meter (m) radius around the rural residential wells sampled for the study. Samples from residential wells that had four or fewer oil and gas wells in the surrounding 500-m radius had statistically lower concentrations of radium-226, bromide, and ethane than samples from residential wells sampled that had five or more oil and gas wells in the surrounding 500-m radius. Given the available data, the relationship between concentrations of radium-226, bromide, and ethane for wells sampled in this study and oil and gas development or natural geochemical processes is not clear. Groundwater-age tracers (chlorofluorocarbons, tritium, and sulfur hexafluoride) were sampled at 17 of the 30 wells. All 17 samples contained a fraction of young, post-1950s groundwater. Many of the groundwater samples collected for this study have high calcium to sodium ratios and low total dissolved solids concentrations, indicating they are dominated by recently recharged water. A subset of samples had chloride to bromide mass ratios between 70 and 200, indicating that deep Appalachian basin brines mixed with the shallow groundwater. For most of the samples in this study, the C 1 through C 6 hydrocarbons have characteristics that reflect a biogenic gas signature that has, to varying degrees, undergone oxidation processes during transport. None of the samples show a characteristic thermogenic cracking pattern among the hydrocarbon ratios.

West Virginia↗

USGS2017

Have mummichog (Fundulus heteroclitus) from the lower Penobscot River, Maine, developed tolerance to the toxic effects of mercury?

Fish populations that are chronically exposed to mercury (Hg) can develop resistance to the toxic effects of this metal, including mummichog (Fundulus heteroclitus; Weis 2002). Such resistance allows them to potentially accumulate very high levels of this contaminant (Stefansson et al. 2013). Mercury is a neurotoxin that affects behavior in fish, including swimming and the ability to capture prey (Samson et al. 2001, Zhou et al. 2001), and behavior, reproduction and immune function in birds (Evers et al. 2008, Hawley et al. 2009). Ingestion of mercury-contaminated prey could have significant, and severe, effects on migratory fish and piscivorous birds, including loons (Evers et al. 2008). We found that mercury concentrations in resident mummichog collected from sites in the lower Penobscot River in 2011 were 9 to 16 times higher than Hg levels in mummichog from a control site in Wells, Maine (Elskus 2012). For part one of this study, reproductively mature male and female mummichog were collected in Fall 2015 from two sites in Maine: Bald Hill Cove, a mercury-contaminated site along the mercury gradient of the Penobscot River, and Drake, a reference site at the Wells National Estuarine Research Reserve. These parental fish were housed at the US EPA laboratory (Narragansett, RI). Beginning in Spring 2016, these fish were fed diets containing either low or high concentrations of mercury for 28 days. Embryos were collected from these parents and divided into subsets. One subset was used to measure the mercury concentrations in the embryos, the second subset was shipped to the University of Maine where they were hatched, and the larval fish evaluated for behavioral effects. For part two of this study, adult mummichog were collected from Hg-contaminated Bald Hill Cove and from a reference site, Wells, in the Wells National Estuarine Reserve and evaluated for mercury body burdens and behavior. In Study 1, mercury was maternally transferred to the progeny demonstrating this is one pathway of generational exposure to mercury. Unfortunately, all larvae from the mercury-contaminated Bald Hill Cove population died before behavioral analysis could be done. Behavioral studies of the reference Drake population, however, demonstrated no significant differences between offspring of parents fed high mercury diets and offspring of parents fed low mercury diets. In Study 2, adult fish from the mercury contaminated BHC population had mercury body burdens that were four times higher than those in the reference Wells population, but while fewer BHC adults performed prey strikes than the Wells adults, there were no other significant behavioral differences between the two populations. In conclusion, the main hypothesis, that fish from the site receiving chronic mercury exposure had developed resistance to mercury toxicity, could not be definitively determined due to the death of embryos from the chronically exposed population. However, the present study did reveal some behavioral effects associated with mercury exposure that warrant further study. Behavioral approaches are important because they address some of the basic and difficult questions surrounding contaminant exposures; namely that sub-lethal effects are important to evaluate because they may have consequences for individual and perhaps population survival.

Maine↗

USGS1987

Surface-water quality in Pequea Creek basin, Pennsylvania, 1977-79

A study of the Pequea Creek basin was conducted by the U.S. Geological Survey, in cooperation with the Susquehanna River Basin Commission and the EPA from February 1977 through March 1979. Pequea Creek drains an intensive agricultural area of 154 sq mi in southeastern Pennsylvania, and enters the Susquehanna River 30 mi north of the Chesapeake Bay. The study included measurement of streamflow and collection of water and bottom material samples from seven sites in the basin during selected base flows and storms. Water samples were collected daily at a site near the mouth of Pequea Creek, and analyzed for suspended sediment, nitrogen and phosphorus species, organic carbon, and pesticides. Some groundwater samples also were collected and analyzed for nitrate. Annual yields measured from the basin during the study period were 1,950 ton/sq mi for suspended sediment, 13.8 ton/sq mi for total nitrogen, and 1.8 ton/sq mi for phosphorus. These yields are five times higher than any previously measured in the Susquehanna River basin. The discharges of all constituents monitored increased with increasing flow, indicated that a large amount of material in the basin is available for transport to streams during storms. The large yields of nitrogen and phosphorus are probably caused by the intensive agriculture in the basin coupled with large applications of fertilizer and manure to farm fields. Chemical analyses of rainfall samples indicate that precipitation was not a significant source of nitrogen and phosphorus. Excluding nitrate, all constituents measured were transported mainly during storms. Nitrate concentrations during base flow were as high as 10 mg/L as N--the Environmental Protection Agency standard for domestic water supplies. Groundwater sampled from farm wells had nitrate concentrations up to 28 mg/L as N. The largest concentrations of herbicides detected in Pequea basin were for 2,4-D, atrazine, and simazine. The maximum concentrations observed during storms were 1.2, 24, and 5.4 micrograms/L, respectively. The insecticides chlordane and DDT had mean concentrations of 0.02 and 0.01 micrograms/L, respectively. Lindane, PCB, and heptachlor slightly exceed maximum limits during storms.

Pennsylvania↗

USGS2010

Land-cover change in the Ozark Highlands, 1973-2000

Led by the Geographic Analysis and Monitoring Program of the U.S. Geological Survey (USGS) in collaboration with the U.S. Environmental Protection Agency (EPA) and the National Aeronautics and Space Administration (NASA), the Land-Cover Trends Project was initiated in 1999 and aims to document the types, geographic distributions, and rates of land-cover change on a region by region basis for the conterminous United States, and to determine some of the key drivers and consequences of the change (Loveland and others, 2002). For 1973, 1980, 1986, 1992, and 2000 land-cover maps derived from the Landsat series are classified by visual interpretation, inspection of historical aerial photography and ground survey, into 11 land-cover classes. The classes are defined to capture land cover that is discernable in Landsat data. A stratified probability-based sampling methodology undertaken within the 84 Omernik Level III Ecoregions (Omernik, 1987) was used to locate the blocks, with 9 to 48 blocks per ecoregion. The sampling was designed to enable a statistically robust 'scaling up' of the sample-classification data to estimate areal land-cover change within each ecoregion (Loveland and others, 2002; Stehman and others, 2005). At the time of writing, approximately 90 percent of the 84 conterminous United States ecoregions have been processed by the Land-Cover Trends Project. Results from these completed ecoregions illustrate that across the conterminous United States there is no single profile of land-cover/land-use change, rather, there are varying pulses affected by clusters of change agents (Loveland and others, 2002). Land-Cover Trends Project results for the conterminous United States to-date are being used for collaborative environmental change research with partners such as; the National Science Foundation, the National Oceanic and Atmospheric Administration, and the U.S. Fish and Wildlife Service. The strategy has also been adapted for use in a NASA global deforestation initiative, and elements of the project design are being used in the North American Carbon Program's assessment of forest disturbance.

Open-File Report↗

USGS2016

The effectiveness of water-treatment systems for arsenic used in 11 homes in Southwestern and Central Ohio, 2013

In 2013, the U.S. Geological Survey and the Miami Conservancy District investigated the effectiveness of methods used to remove arsenic from drinking water at 11 homes in southwestern and central Ohio. The untreated (raw) ground-water had arsenic concentrations of 7.7–382 micrograms per liter (µg/L), and the median concentration was 30 µg/L. The pH was neutral to slightly alkaline, and redox conditions were strongly reducing, as indicated by high concentrations of iron. The predominant arsenic species was arsenite (As 3+ ), which is difficult to treat because it exists in water as an uncharged compound (H 3 AsO 3 ). The water-treatment systems included (1) seven single-tap reverse-osmosis systems, (2) two whole-house oxidation/filtration systems, and (3) two systems that included wholehouse anion exchange and single-tap reverse osmosis. All but one system included pretreatment by a water softener, and two systems included preoxidation to convert arsenite (As 3+ ) to arsenate (As 5+ ) before treatment by anion exchange. None of the treatment systems removed all of the arsenic from the drinking water. About one-half of the systems decreased the arsenic concentration to less than the maximum contamination level of 10 µg/L. The effectiveness of the systems varied widely; the percentage of arsenic removed ranged from 2 to 90 percent, and the median was 65 percent. At some sites, the low effectiveness of arsenic removal may have been related to system maintenance and(or) operation issues. At two sites, homeowners acknowledged that the treatment systems had not been maintained for several years. At two other sites, the treatment systems were being maintained, but the water-quality data indicated that one of the components was not working, unbeknownst to the homeowner. EPA research at a small number of sites in Ohio indicated that operation and maintenance of some arsenic-treatment systems was not always simple. Another factor that affected system effectiveness was the quality of the raw water. In general, the treatment systems were less effective at treating higher concentrations of arsenic. For five sites with raw-water arsenic concentrations of 10–30 µg/L, the systems removed 65–81 percent of the arsenic, and the final concentrations were less than the maximum contamination level. For three sites with higher raw-water arsenic concentrations (50–75 µg/L), the systems removed 22–34 percent of the arsenic; and the final concentrations were 4–5 times more than the maximum contamination level. Other characteristics of the raw water may have affected the performance of treatment systems; in general, raw water with the higher arsenic concentrations also had higher pH, higher concentrations of organic carbon and ammonia, and more reducing (methanogenic) redox conditions. For sites with raw-water arsenic concentrations of 10–30 µg/L, two types of systems (reverse osmosis and oxidation/filtration) removed similar amounts of arsenic, but the quality of the treated water differed in other respects. Reverse osmosis caused substantial decreases in pH, alkalinity, and concentrations of most ions. On the other hand, oxidation/filtration using manganese-based media caused a large increase of manganese concentrations, from less than 50 µg/L in raw water to more than 700 µg/L in outflow from the oxidation filtration units. It is not known if the results of this study are widely applicable; the number of systems sampled was relatively small, and each system was sampled only once. Further study may be warranted to investigate whether available methods of arsenic removal are effective/practical for residential use in areas like Ohio, were groundwater with elevated arsenic concentrations is strongly reducing, and the predominant arsenic species is arsenite (As 3+ ).

Ohio↗

USGS2014

Estimation of regional flow-duration curves for Indiana and Illinois

Flow-duration curves (FDCs) of daily streamflow are useful for many applications in water resources planning and management but must be estimated at ungaged sites. One common technique for estimating FDCs at ungaged sites in a given region is to use equations obtained by linear regression of FDC quantiles against multiple basin characteristics that can be computed by means of a geographic information system (GIS) computer program. In this study, such regional regression equations for estimating FDC quantiles were computed at the 0.1, 0.2, 0.5, 1, 2, 5, 10, 20, 25, 30, 40, 50, 60, 70, 75, 80, 90, 95, 98, 99, 99.5, 99.8, and 99.9-percent exceedance probabilities for rural, unregulated streams in Indiana and Illinois with temporally stationary records, using data through September 30, 2007. The approach used accounts for censored values below 0.01 cubic feet per second, which are observed at exceedance probabilities as low as 70 percent (that is, occurring at least 30 percent of the time). The basin characteristics used are suitable for computation by the USGS Web-based application, StreamStats, and are available for all U.S. Environmental Protection Agency (EPA) Region V states and the larger Great Lakes area, with some specific local exceptions. Indiana and Illinois were each divided into three regions, and a different set of equations for estimating FDC quantiles was computed for each region. The error of estimation of the FDC quantiles, measured as the mean square residual in log space converted to a percentage of the quantile, varies somewhat among regions and varies strongly with exceedance probability, with a minimum error of 10 to 20 percent at an exceedance probability of 5 or 10 percent, but rises to 17 to 38 percent at the high-flow end of the FDCs (the 0.1-percent quantile) and 100 to 745 percent at the low-flow end. For comparison, errors of estimation also were computed for FDC quantiles estimated by linear regression on drainage area alone and by using the drainage-area ratio (DAR) method. Three criteria, the nearest basin centroid and two others termed “strict” and “broad”, were used to select index stations for the DAR method. The “strict” and “broad” criteria put conditions on the basin centroid distance and the range of their drainage-area ratios, and the errors were averaged for all index station pairs satisfying each criterion. The use of the simpler DAR method usually resulted in higher errors of estimation compared to the linear regression equations with multiple basin characteristics, except occasionally in the case of the DAR method with the strict index station selection criterion, a criterion that is rarely possible to satisfy in practice. An example application of the estimated equations to one gaged and a few ungaged locations in a watershed in the study area is included to illustrate the steps required. These steps are the computation of the basin characteristics and, using those characteristics together with the estimated equations, the computation of the FDC quantiles and their uncertainties.

Illinois, Indiana↗

USGS2015

Chloride concentrations, loads, and yields in four watersheds along Interstate 95, southeastern Connecticut, 2008-11: factors that affect peak chloride concentrations during winter storms

Chloride (Cl - ) concentrations and loads and other water chemistry characteristics were assessed to evaluate potential effects of road-deicer applications on streamwater quality in four watersheds along Interstate 95 (I–95) in southeastern Connecticut from November 1, 2008, through September 30, 2011. Streamflow and water quality were studied in the Four Mile River, Oil Mill Brook, Stony Brook, and Jordan Brook watersheds, where developed land ranged from 9 to 32 percent. Water-quality samples were collected and specific conductance was measured continuously at paired water-quality monitoring sites, upstream and downstream from I–95. Specific conductance values were related to Cl - concentrations to assist in determining the effects of road-deicing operations on the levels of Cl - in the streams. Streamflow and water-quality data were compared with weather data and with the timing, amount, and composition of deicers applied to State highways. Grab samples were collected during winter stormwater-runoff events, such as winter storms or periods of rain or warm temperatures in which melting takes place. Grab samples were also collected periodically during the spring and summer and during base-flow conditions. The estimated Cl - concentrations at the eight water-quality monitoring sites during winter storms peaked as high as 270 milligrams per liter (mg/L) and were well below the U.S. Environmental Protection Agency (EPA) recommended acute chloride toxicity criterion of 860 mg/L and the chronic 4-day average toxicity criterion of 230 mg/L. Cl - concentrations in streams, particularly at sites downstream from I–95, peaked during increased streamflow in the winter and early spring as a result of deicers applied to roads and washed off by stormwater or meltwater. Cl - concentrations during most of the nonwinter seasons decreased during increases in streamflow because storm runoff was more dilute than base flow. However, peaks in specific conductance and estimated chloride concentrations at streams in more urbanized watersheds corresponded to peaks in streamflow well after winter snow or ice events; these delayed peaks in Cl - concentration likely resulted from deicer residue that remained in melting snow piles and on roadsides and (or) that were flushed from soils and shallow groundwater, then discharged downstream. Estimated peak Cl - concentrations varied with the type of winter storm event and were highest during or after winter storms of frozen precipitation and rain, in which the rain or meltwater effectively washed off the deicers. Estimated peak Cl - concentrations correlated positively with the duration of deicer application but generally not with streamflow. Estimated peak Cl - concentrations during the winter season were highest during low streamflow at most sites. Chloride concentrations varied considerably in shallow groundwater as a result of land-use differences. Cl - concentrations were very high (as high as 800 mg/L) in shallow groundwater downstream from I–95 at the Four Mile River site. Chloride/bromide mass concentration ratios and the proximity of a former landfill and sewage lagoon upstream indicate a likely source of Cl - is landfill leachate and possibly sewage leachate. Cl - loads in streams generally were highest in the winter and early spring. The estimated daily Cl - yield for the four monitoring sites downstream from I–95 ranged from 0.0004 ton per day per square mile for one of the least developed watersheds to 0.052 ton per day per square mile for the watershed with the highest percentage of urban development and impervious area. The estimated median contribution of Cl - load from atmospheric deposition was small and ranged from 0.07 percent of Cl - load at the Jordan Brook watershed to 0.57 percent at the Oil Mill Brook watershed. The Cl - loads in streams (outputs) were compared with Cl - load inputs, which include atmospheric deposition and deicer applications; Cl - load inputs were slightly larger than the Cl - load outputs at most of the sites during most years but do not account for the Cl - load in groundwater leaving the watersheds. A multiple linear regression model was developed to describe the variability of the natural log of peak specific conductance, as well as estimated Cl - concentrations. Five significant variables best explained the variability in the natural log of the peak specific conductance after deicing events: (1) snow on ground before deicing event; (2) winter precipitation with rain; (3) specific conductance in base flow; (4) State-operated road lane miles divided by watershed area; and (5) amount of Cl - from deicers applied to State-operated roads per lane mile. In this report, winter precipitation is defined as any type of precipitation, including frozen precipitation and rain, that occurs during the active deicing season, typically November through March. Frozen precipitation is defined here as snow, sleet, freezing rain, or any winter precipitation except rain. The addition of a lane mile in both directions on I–95 would result in an estimate of approximately 2 to 11 percent increase in Cl - input from deicers applied to I–95 and other roads maintained by Connecticut Department of Transportation. The largest estimated increase in Cl - load was in the watersheds with the greatest number miles of I–95 corridor relative to the total lane miles maintained by Connecticut Department of Transportation. On the basis of these estimates and the estimated peak Cl - concentrations during the study period, it is unlikely that the increased use of deicers on the additional lanes would lead to Cl - concentrations that exceed the aquatic habitat criteria.

Connecticut↗

USGS2014

Urban ecosystem services and decision making for a green Philadelphia

Traditional approaches to urban development often do not account for, or recognize, the role of ecosystem services and the benefits these services provide to the health and well-being of city residents. Without such accounting, urban ecosystem services are likely to be degraded over time, with negative consequences for the sustainability of cities and the well-being of their residents (Millennium Ecosystem Assessment, 2005; Hirsch, 2008). On May 23, 2013, the Spatial Integration Laboratory for Urban Systems (SILUS), a collaboration between the U.S. Geological Survey (USGS) Science and Decisions Center and the Wharton GIS Lab, convened a one-day symposium—Urban Ecosystem Services and Decision Making: A Green Philadelphia—at the University of Pennsylvania in Philadelphia, Pennsylvania, to examine the role of green infrastructure in the environmental, economic, and social well-being of cities. Cosponsored by the USGS and the Penn Institute for Urban Research (Penn IUR), the symposium brought together policymakers, practitioners, and researchers from a range of disciplines to advance a research agenda on the use of science in public decision making to inform investment in green infrastructure and ecosystem services in urban areas. The city of Philadelphia has recently implemented a program designed to sustain urban ecosystem services and advance the use of green infrastructure. In 2009, the Philadelphia Mayor’s Office of Sustainability launched its Greenworks plan, establishing a citywide sustainability strategy. Major contributions towards its goals are being implemented in coordination with the Philadelphia Water Department (PWD). The Green City, Clean Waters initiative, the city’s nationally recognized stormwater management plan, was signed into action with the U.S. Environmental Protection Agency (EPA) in April 2012. The plan outlines a 25-year strategy to use green infrastructure to protect and improve the city’s watershed. Widespread support for the plan marks a citywide effort to factor environmental quality concerns into the city’s strategic planning, choosing to replace expensive and aging grey infrastructure, with innovative and resilient green infrastructure. The symposium focused on these city of Philadelphia initiatives and also on two new Federal- local partnership programs: America’s Great Outdoors, initiated to promote conservation and recreation, and the Urban Waters Federal Partnership, a multiagency effort to reconnect urban communities to their waterways. A second goal of the symposium was to advance a research agenda on urban ecosystem services. While there has been considerable work on ecosystem services, the discussion of the benefits provided by urban ecosystems is not as developed. Benefits range from improved water and air quality to quality of life gains, including aesthetic and recreational considerations. There is also need for additional focused research toward furthering the understanding of the multiple indirect benefits provided by urban ecosystem services (Bolund and Hunhammar, 1999). Moreover, there is a need for a greater understanding of how best to inform local decision making in this area, as local decision makers in cities across the country are increasingly recognizing the importance of developing sustainability measures for their immediate and long-term planning (United States Conference of Mayors, 2005). Approaching these local and regional plans from a holistic perspective has become a guiding principle of sustainability and resiliency. Therefore, there is a need to better understand the gains that have been achieved and to advance a research agenda on ecosystem services going forward. The day’s program included presentations on greening initiatives from the Philadelphia’s Mayor’s Office of Sustainability, as well as discussion about using an urban ecosystem services framework to evaluate these initiatives. Panel sessions included discussion of the Green City, Clean Waters initiative; a dialogue about the management of urban trees and green space; and a conversation addressing the needs for future research.

Pennsylvania↗

USGS2012

Primer for identifying cold-water refuges to protect and restore thermal diversity in riverine landscapes

In 2003, EPA issued Region 10 guidance for Pacific Northwest state and tribal temperature water quality standards. This document was the culmination of a multi-agency, multi-disciplinary effort to develop a temperature standard for the protection of salmon, steelhead, bull trout, and redband and Lahontan cutthroat trout (collectively termed coldwater salmonids). Since its release, the Oregon and Washington have adopted the temperature standard for their waters designated for protection of coldwater salmonids. One of the unique aspects of the temperature standard, which strived to integrate the physical nature of rivers and streams and the biological requirements of coldwater salmonids, is the requirement to protect and restore cold-water refuges. This requirement is incorporated into the temperature criterion for the protection of migration corridors in the Willamette, Columbia, and Snake rivers. The intent of this provision is the recognition that some coldwater salmonids migrate through waters during thermally stressful months of summer and most likely are able to do so by using features in the rivers that provide cold water spatially or temporally. The challenge is to ensure that these features are identified, protected, and restored in order for these waters to meet the temperature standard. This primer is intended to assist Region 10 states, tribes, and local watershed groups in meeting this goal and thereby further the protection and restoration of coldwater salmonids. It provides an up-to-date summary with easily referenced information and illustrations on the scientific advances and management applications of research on cold-water refuges and can be used as a "roadmap" for identifying cold-water refuges and learning more about processes that create thermal diversity in riverine landscapes. The specific objectives are to 1. define cold-water refuge in scientific and management contexts. 2. outline an approach for identifying cold-water refuges to address water quality standards. 3. classify and characterize the types and physical processes that create cold-water refuges. 4. review methods and tools for identifying cold-water refuges in small streams to large rivers. 5. describe ecological perspectives and on-the-ground approaches for protecting and restoring thermal diversity in rivers.

Oregon↗