Search USGS⌕ Search

SEARCH · Search USGS

Results for “Analytical Methods”

Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 469 records · Page 26Linked to original sources
USGS2023

Maps of elevation of top of Pierre Shale and surficial deposit thickness with hydraulic properties from borehole geophysics and aquifers tests within and near Ellsworth Air Force Base, South Dakota, 2020–21

The U.S. Geological Survey, in cooperation with the U.S. Air Force Civil Engineer Center, collected borehole geophysical data and completed simple aquifer tests to estimate the thickness and hydraulic properties of surficial deposits. The purpose of data collection was to create generalized contour maps of Pierre Shale elevation and surficial deposit thickness within and near Ellsworth Air Force Base (study area). Natural gamma and electromagnetic induction data were collected to refine or determine surficial deposit thickness at selected wells. Additionally, data from previous geophysical studies and driller logs were compiled and combined with results from natural gamma and electromagnetic induction data to provide a more spatially complete image of the subsurface. Borehole nuclear magnetic resonance (bNMR) data were collected to estimate hydraulic conductivity and water content of surficial deposits overlying Pierre Shale. Simple aquifer tests using water slugs (slug tests) were completed to estimate hydraulic conductivity of surficial deposits, and results were compared to hydraulic conductivity estimates from bNMR data. All data used to construct maps and estimate hydraulic properties are provided in an accompanying U.S. Geological Survey data release (available at https://doi.org/10.5066/P9FLR79F ). Generalized contour maps were constructed using results from 26 borehole geophysical logs, 35 geophysical transects from previous studies, and 304 wells with driller logs. Pierre Shale elevation generally followed land-surface topography, sloping from high elevations in the north to lower elevations in the south. Topographic highs of Pierre Shale, where present, could act as groundwater divides that potentially affect groundwater flow direction. Surficial deposit thickness varied spatially and ranged from 0 to 86 feet. Surficial deposits generally were thickest in higher elevation areas near ephemeral streams in the northern part of the study area. Hydraulic conductivity estimated from bNMR results using two analytical methods ranged from 0.1 to 2,314 feet per day, whereas hydraulic conductivity estimated from slug tests ranged from 0.001 to 193 feet per day. Hydraulic conductivity estimates from slug tests were plotted with surficial deposit thickness contours instead of bNMR estimates because bNMR estimates were determined to overestimate hydraulic conductivity. Hydraulic conductivity values generally were greater in the southwestern part of study area than the northeastern part.

South Dakota↗
USGS2004

Characterization of Ground-Water Quality, Upper Republican Natural Resources District, Nebraska, 1998-2001

Nearly all rural inhabitants and livestock in the Upper Republican Natural Resources District (URNRD) in southwestern Nebraska use ground water that can be affected by elevated nitrate concentrations. The development of ground-water irrigation in this area has increased the vulnerability of ground water to the introduction of fertilizers and other agricultural chemicals. In 1998, the U.S. Geological Survey, in cooperation with the Upper Republican Natural Resources District, began a study to characterize the quality of ground water in the Upper Republican Natural Resources District area with respect to physical properties and concentrations of major ions, coliform bacteria, nitrate, and pesticides, and to assess the presence of nitrogen concentrations in the unsaturated zone. At selected well sites, the ground-water characterization also included tritium and nitrogen-isotope analyses to provide information about the approximate age of the ground water and potential sources of nitrogen detected in ground-water samples, respectively. In 1998, ground-water samples were collected from 101 randomly selected domestic-well sites. Of the 101 samples collected, 26 tested positive for total coliform bacteria, exceeding the U.S. Environmental Protection Agency's Maximum Contaminant Level (MCL) of zero colonies. In 1999, ground-water samples were collected from 31 of the 101 well sites, and 16 tested positive for coliform bacteria. Nitrates were detected in ground water from all domestic-well samples and from all but four of the irrigation-well samples collected from 1998 to 2001. Eight percent of the domestic-well samples and 3 percent of the irrigation-well samples had nitrate concentrations exceeding the U.S. Environmental Protection Agency's MCL for drinking water of 10 milligrams per liter. Areas with nitrate concentrations exceeding 6 milligrams per liter, the URNRD's ground-water management-plan action level, were found predominantly in north-central Chase, western and south-central Dundy, and south-central Perkins Counties. Generally, these concentrations were detected in samples from wells located in upland areas with permeable soils and a high percentage of cropland. In 1999, 31 of the ground-water samples collected from irrigation wells were analyzed for pesticides, and 14 samples (45 percent) had detectable concentrations of at least one pesticide compound. In 2000, all of the 23 irrigation-well samples analyzed had one or more pesticides present at detectable concentrations. In 2001, 12 of 26 domestic-well samples (46 percent) had detectable concentrations. Although the analytical method used during the study was changed to increase the number of pesticides included in the analyses, the pesticides detected in the ground-water samples from domestic and irrigation wells were limited to the commonly used herbicide compounds acetochlor, alachlor, atrazine, metolachlor, prometon, propachlor, propazine, trifluralin, and the atrazine degradation product deethylatrazine. Of the compounds detected, only atrazine (3.0 micrograms per liter) and alachlor (2.0 micrograms per liter) have MCLs established by the U.S. Environmental Protection Agency. None of the ground-water samples from the URNRD study area had concentrations that exceeded either MCL. Tritium age-dating analyses indicate water from about one-third of the sites entered the ground-water system prior to 1952. Because the increase in agricultural practices occurred during the 1950s and 1960s, it can be assumed that this water was not influenced by agricultural practices. Nitrogen-isotope speciation analyses for samples from three irrigation wells indicated that the source of nitrates in the ground water probably is synthetic fertilizer; however, the source at most irrigation wells probably is either naturally occurring or a mixture of water from various anthropogenic sources (such as synthetic fertilizer and animal waste).

Scientific Investigations Report↗
USGS2004

Water Quality of the Snake River and Five Eastern Tributaries in the Upper Snake River Basin, Grand Teton National Park, Wyoming, 1998-2002

To address water-resource management objectives of the National Park Service in Grand Teton National Park, the U.S. Geological Survey in cooperation with the National Park Service has conducted water-quality sampling in the upper Snake River Basin. Routine sampling of the Snake River was conducted during water years 1998-2002 to monitor the water quality of the Snake River through time. A synoptic study during 2002 was conducted to supplement the routine Snake River sampling and establish baseline water-quality conditions of five of its eastern tributaries?Pilgrim Creek, Pacific Creek, Buffalo Fork, Spread Creek, and Ditch Creek. Samples from the Snake River and the five tributaries were collected at 12 sites and analyzed for field measurements, major ions and dissolved solids, nutrients, selected trace metals, pesticides, and suspended sediment. In addition, the eastern tributaries were sampled for fecal-indicator bacteria by the National Park Service during the synoptic study. Major-ion chemistry of the Snake River varies between an upstream site above Jackson Lake near the northern boundary of Grand Teton National Park and a downstream site near the southern boundary of the Park, in part owing to the inputs from the eastern tributaries. Water type of the Snake River changes from sodium bicarbonate at the upstream site to calcium bicarbonate at the downstream site. The water type of the five eastern tributaries is calcium bicarbonate. Dissolved solids in samples collected from the Snake River were significantly higher at the upstream site (p-value<0.001), where concentrations in 43 samples ranged from 62 to 240 milligrams per liter, compared to the downstream site where concentrations in 33 samples ranged from 77 to 141 milligrams per liter. Major-ion chemistry of Pilgrim Creek, Pacific Creek, Buffalo Fork, Spread Creek, and Ditch Creek generally did not change substantially between the upstream sites near the National Park Service boundary with the National Forest and the downstream sites near the Snake River; however, variations in the major ions and dissolved solids existed between basins. Variations probably result from differences in geology between the tributary basins. Concentrations of dissolved ammonia, nitrite, and nitrate in all samples collected from the Snake River and the five eastern tributaries were less than water-quality criteria for surface waters in Wyoming. Concentrations of total nitrogen and total phosphorus in samples from the Snake River and the tributaries generally were less than median concentrations determined for undeveloped streams in the United States; however, concentrations in some samples did exceed ambient total-nitrogen and total-phosphorus criteria for forested mountain streams in the Middle Rockies ecoregion recommended by the U.S. Environmental Protection Agency to address cultural eutrophication. Sources for the excess nitrogen and phosphorus probably are natural because these basins have little development and cultivation. Concentrations of trace metals and pesticides were low and less than water-quality criteria for surface waters in Wyoming in samples collected from the Snake River and the five eastern tributaries. Atrazine, dieldrin, EPTC, or tebuthiuron were detected in estimated concentrations of 0.003 microgram per liter or less in 5 of 27 samples collected from the Snake River. An estimated concentration of 0.008 microgram per liter of metolachlor was detected in one sample from the Buffalo Fork. The estimated concentrations were less than the reporting levels for the pesticide analytical method. Suspended-sediment concentrations in 43 samples from the upstream site on the Snake River ranged from 1 to 604 milligrams per liter and were similar to suspended-sediment concentrations in 33 samples from the downstream site, which ranged from 1 to 648 milligrams per liter. Suspended-sediment concentrations in 38 samples collected from the tributary streams ranged from 1 t

Scientific Investigations Report↗
USGS2005

Summary of significant results from studies of triazine herbicides and their degradation products in surface water, ground water, and precipitation in the midwestern United States during the 1990s

Nonpoint-source contamination of water resources from triazine herbicides has been a major water-quality issue during the 1990s in the United States. To address this issue, studies of surface water, ground water, and precipitation have been carried out by the U.S. Geological Survey in the Midwestern United States. Reconnaissance studies of 147 streams were conducted to determine the geographic and seasonal distribution of atrazine, cyanazine, propazine, and simazine. These studies showed that high concentrations of herbicides were flushed from cropland and transported through the stream system as pulses in response to spring and summer rainfall. The studies also revealed the persistence of herbicides and their degradation products in streams. An investigation of 76 reservoirs showed that the occurrence and temporal distribution of herbicides and their degradation products in reservoir outflow could be related to reservoir and drainage-basin characteristics, water and land use, herbicide use, and climate. Significant findings showed that concentrations of atrazine and its degradation products remained elevated all summer and into the fall and that recently applied atrazine mixed with atrazine applied the previous year as water moved through a reservoir. Reconnaissance studies of 303 ground-water wells were completed to determine hydrogeological and seasonal occurrence, concentration, and distribution of herbicides and their degradation products. Samples collected from across the Midwestern United States consistently revealed that triazine herbicide degradation products commonly were found more frequently than their parent herbicide and that ground-water age could be an important factor in explaining variations in herbicide contamination. A final study investigated precipitation in the Midwestern United States, northeast to the Atlantic Ocean, and northward to the Canadian border. It found that the highest herbicide concentrations in precipitation occurred following herbicide application to cropland. Atrazine was detected most often, followed by deethylatrazine, cyanazine, and deisoproplyatrazine. Mass deposition of herbicides by precipitation was greatest in areas where herbicide use was intense and decreased with distance from the Midwest. Findings of the 1990s studies include an improved understanding of the occurrence, persistence, chemistry, and transport of triazine herbicides and their degradation products in the hydrologic environment. A significant increase in knowledge of triazine herbicides and development and improvement of analytical methods were accomplished in the past decade. The results produced are not only significant for the present (2005) but provide an important data set for future use.

Midwest region↗
USGS2005

Comparability of suspended-sediment concentration and total suspended-solids data for two sites on the L'Anguille River, Arkansas, 2001 to 2003

Suspended-sediment concentration and total suspended solids data collected with automatic pumping samplers at the L'Anguille River near Colt and the L'Anguille River at Palestine, Arkansas, August 2001 to October 2003 were compared using ordinary least squares regression analyses to determine the relation between the two datasets for each of the two sites. The purpose of this report is to describe the suspended-sediment concentration and total suspended-solids data and examine the comparability of the two datasets for each site. Suspended-sediment concentration and total suspended solids data for the L'Anguille River varied spatially and temporally from August 2001 to October 2003. The site at the L'Anguille River at Palestine represents a larger portion of the L'Anguille River Basin than the site near Colt, and generally had higher median suspended-sediment concentration and total suspended solids and greater ranges in values. The differences between suspended-sediment concentration and total suspended solids data for the L'Anguille River near Colt appeared inversely related to streamflow and not related to time. The relation between suspended-sediment concentration and total suspended solids at the L'Anguille River at Palestine was more variable than at Colt and did not appear to have a relation with flow or time. The relation between suspended-sediment concentration and total suspended solids for the L'Anguille River near Colt shows that total suspended solids increased proportionally as suspended-sediment concentration increased. However, the relation between suspended-sediment concentration and total suspended solids for the L'Anguille River at Palestine showed total suspended solids increased less proportionally as suspended-sediment concentration increased compared to the L'Anguille River near Colt. Differences between the two analytical methods may partially explain differences between the suspended-sediment concentration and total suspended solids data at the two sites. Total suspended solids are analyzed by removing an aliquot of the original sample for further analysis, and suspended-sediment concentrations are analyzed using all sediment and the total mass of the sample. At the L'Anguille River at Palestine another source of variability in the two data sets could have been the location of the automatic pumping sampler intake. The intake was located at a point in the stream cross-section that was subject to sedimentation, which may have resulted in positive sample bias.

Scientific Investigations Report↗
USGS2005

Occurrence of organic wastewater compounds in wastewater effluent and the Big Sioux River in the Upper Big Sioux River basin, South Dakota, 2003-2004

The U.S. Geological Survey (USGS) in cooperation with the East Dakota Water Development District conducted a reconnaissance study to determine the occurrence of organic wastewater compounds (OWCs) in wastewater effluent and the Big Sioux River at or near the cities of Watertown, Volga, and Brookings in the upper Big Sioux River Basin during August 2003 through June 2004. For each city, samples were collected from the wastewater treatment plant (WWTP) effluent and from Big Sioux River sites upstream and downstream from where the wastewater effluent discharges to the Big Sioux River. For Watertown and Brookings, samples were collected during a low-flow period (August 2003) and a runoff period (June 2004). For Volga, samples were collected during two low-flow periods (August 2003 and October 2003) and a runoff period (June 2004). A total of 125 different OWCs were analyzed for and were classified into six compound classes-human pharmaceutical compounds (HPCs), human and veterinary antibiotic compounds (HVACs), major agricultural herbicides (MAHs), household, industrial, and minor agricultural compounds (HIACs), polyaromatic hydrocarbons (PAHs), and sterol compounds (SCs). Of the 125 different OWCs, 45 had acceptable analytical method performance, were detected at concentrations greater than the study reporting levels, and were included in analyses and discussion related to occurrence of OWCs in wastewater effluents and the Big Sioux River. OWCs in all six compound classes were detected in water samples from sampling sites in the Watertown area. The Watertown WWTP discharged continuously to the Big Sioux River during both the low-flow August 2003 and runoff June 2004 sampling periods. Total OWC concentrations for Big Sioux River sites upstream from the Watertown WWTP discharge generally were small, less than 6 micrograms per liter (µg/L) for both sampling periods. SCs accounted for nearly all of the total OWC concentrations for upstream Big Sioux River sites for the low-flow August 2003 sampling period, and MAHs accounted for nearly all of the total OWC concentrations for the runoff June 2004 sampling period. Total OWC concentrations for samples collected from the Watertown wastewater effluent were relatively large for both sampling periods (estimated concentrations ranged from 20 to 41 µg/L), and primarily consisted of HIACs, SCs, and HVACs. Total OWC concentrations for Big Sioux River sites downstream from the Watertown WWTP discharge were relatively large for the low-flow August 2003 sampling period (estimated concentrations ranged from 6.9 to 19 µg/L) and smaller for the runoff June 2004 sampling period (estimated concentrations ranged from 3.3 to 6.5 µg/L), a pattern that probably reflects a greater fraction of the total flow of the Big Sioux River being derived from WWTP discharge during the low-flow sampling period. Major OWC classes contributing to total OWC concentrations for Big Sioux River sites downstream from the Watertown WWTP were HIACs, SCs, and HVACs. Total OWC concentrations decreased substantially between the two downstream Big Sioux River sites. Although confident conclusions could not be made primarily due to possible effects of non-Lagrangian sampling, OWC results for the Watertown area might indicate that (1) OWCs for upstream Big Sioux River sites probably were primarily contributed by nonpoint agricultural sources, with livestock agriculture accounting for most of the total OWC concentration for the low-flow August 2003 sampling period, and crop agriculture accounting for most of the total OWC concentration for the runoff June 2004 sampling period; (2) OWCs for downstream Big Sioux River sites were substantially influenced by contributions from the Watertown WWTP during both the low-flow and runoff sampling periods; and (3) contributions of OWCs that might be derived from nonpoint livestock agricultural sources increased in proportion for the most downstream site for both the low-flow and runoff sampling periods. Suspected endocrine-disrupting compounds (EDCs) were detected in all Big Sioux River samples in the Watertown area. For both the low-flow and runoff sampling periods, the numbers of EDCs detected, and EDC concentrations and loads generally were larger for downstream Big Sioux River sites than for upstream Big Sioux River sites. Combined EDC concentrations for downstream Big Sioux River sites consisted mostly of HIACs for the low-flow sampling period and both HIACs and MAHs for the runoff sampling period. OWCs in all compound classes except PAHs were detected in samples from sites in the Volga area. The Volga WWTP was not discharging to the Big Sioux River during the low-flow August 2003 and runoff June 2004 sampling periods, but was discharging continuously to the Big Sioux River during the low-flow October 2003 sampling period. For the low-flow August 2003 sampling period, the upstream Big Sioux River site had larger total OWC concentrations and loads than downstream Big Sioux River sites, and SCs accounted for most of the total OWC concentration for all Big Sioux River sites. For the low-flow October 2003 sampling period, when the Volga WWTP was discharging to the Big Sioux River, total OWC concentrations and loads were larger for the downstream Big Sioux River site than for the upstream site, and the increase in load corresponded well with the load contributed by the Volga wastewater effluent discharge, especially for HIACs. HIACs and SCs accounted for most of the total OWC concentrations for Big Sioux River sites for the October 2003 sampling period. For the June 2004 runoff sampling period, the upstream Big Sioux River site had smaller total OWC concentrations and loads than downstream Big Sioux River sites, and MAHs accounted for most of the total OWC concentrations for all Big Sioux River sites. Although confident conclusions could not be made due to possible effects of non-Lagrangian sampling, the data might indicate that (1) for the low-flow August 2003 sampling period, nonpoint livestock agricultural and/or human wastewater sources might have been the primary contributors to occurrence of OWCs at Big Sioux River sampling sites; (2) for the low-flow October 2003 sampling period, nonpoint livestock sources and upstream human wastewater sources primarily contributed to occurrence of OWCs at Big Sioux River sampling sites; (3) for the runoff June 2004 sampling period, nonpoint crop agricultural sources primarily contributed to occurrence of OWCs at Big Sioux River sampling sites; (4) for the low-flow August 2003 and runoff June 2004 sampling periods, seepage of water from the Volga WWTP had little effect on downstream OWC concentrations; and (5) for the low-flow October 2003 sampling period, the Volga wastewater effluent discharge contributed to downstream OWC concentrations. EDCs were detected in all samples collected from sampling sites in the Volga area. For all sampling periods, total EDC concentrations generally were similar between upstream and downstream Big Sioux River sites and consisted of HIACs and MAHs. HIACs accounted for most of the total EDC concentrations for the low-flow August 2003 and October 2003 sampling periods, and MAHs accounted for most of the total EDC concentrations for the runoff June 2004 sampling period for all Big Sioux River sites. OWCs in all compound classes except PAHs were detected in water samples from sampling sites in the Brookings area. The Brookings WWTP discharged continuously to the Big Sioux River during all sampling periods. For the low-flow August 2003 sampling period, the upstream site had slightly smaller total OWC concentrations and loads compared to the downstream Big Sioux River sites. SCs and HIACs accounted for most of the total OWC concentration in all Big Sioux River sampling sites, but the proportion of SCs increased at the most downstream site. For the runoff June 2004 sampling period, the upstream site generally had smaller total OWC concentrations and loads than downstream Big Sioux River sites. MAHs accounted for most of the total OWC concentration for all Big Sioux River sites, but the proportion of SCs increased at the most downstream site. Although confident conclusions could not be made due to possible effects of non-Lagrangian sampling, the data might indicate that (1) for the low-flow August 2003 sampling period, nonpoint livestock agricultural sources probably primarily contributed to occurrence of OWCs at all Big Sioux River sampling sites, and the Brookings WWTP wastewater effluent discharge contributed but did not have a substantial effect on concentrations at downstream sites; and (2) for the runoff June 2004 sampling period, nonpoint crop agricultural sources primarily contributed to occurrence of OWCs at all Big Sioux River sites, contributions of OWCs that might be derived from nonpoint livestock agricultural sources increased in proportion to other sources for the most downstream site, and the Brookings WWTP wastewater effluent discharge probably did not substantially contribute to total OWC concentrations at downstream sampling sites. EDCs were detected in all samples collected from sampling sites in the Brookings area. Total EDC concentrations for the upstream site consisted entirely of MAHs. Total EDC concentrations for downstream sites consisted of MAHs and HIACs. HIACs accounted for most of the total EDC concentrations for the low-flow August 2003 sampling period, and MAHs accounted for most of the total EDC concentrations for the runoff June 2004 sampling period for downstream Big Sioux River sites. The city of Watertown is located near the upstream part of the Big Sioux River Basin, where the mean annual flow of the Big Sioux River is less than 100 cubic feet per second (ft 3 /s). Watertown WWTP discharges can account for a substantial part of the flow in the Big Sioux River, especially during low-flow periods. Effects of the Watertown WWTP wastewater effluent discharges on the occurrence of OWCs in the Big Sioux River downstream were apparent during both the low-flow and runoff sampling periods. For Volga and Brookings, which are farther downstream and where the mean annual flow of the Big Sioux River exceeds 400 ft 3 /s, wastewater effluent discharges from the Volga and Brookings WWTPs probably influenced the occurrence of OWCs in the Big Sioux River, but probably did not substantially contribute to total OWC concentrations, especially during the runoff sampling period.

South Dakota↗
USGS2006

Occurrence of isoxaflutole, acetamide, and triazine herbicides and their degradation products in 10 Iowa rivers draining to the Mississippi and Missouri Rivers, 2004

During 2004, a study to document the occurrence of herbicides and herbicide degradation products was conducted for 10 major Iowa rivers draining to the Missouri and Mississippi Rivers. Seventy-five water-quality samples were collected to measure isoxaflutole, acetamide, and triazine herbicides and their herbicide degradation products. An analytical method to measure isoxaflutole and its degradation products, diketonitrile and benzoic acid, was developed by the U.S. Geological Survey Organic Geochemistry Research Laboratory in Lawrence, Kansas, using vacuum manifold solid-phase extraction and liquid chromatography/mass spectrometry/mass spectrometry and is described in this report. Isoxaflutole, a low application rate preemergence herbicide for control of annual broadleaf weeds, is used extensively in Iowa. Findings from the study documented in this report indicate that isoxaflutole was designed to degrade quickly to diketonitrile, which appears to be more stable, and then to benzoic acid. Of the 75 samples collected to measure isoxaflutole, there were four detections of isoxaflutole, 53 detections of diketonitrile, and 41 detections of benzoic acid. Also, results of acetamide and triazine water-quality samples correlate with past studies, which indicate that herbicide degradation products are detected more frequently and often at higher concentrations in surface water than their parent compounds. In addition to analysis of isoxaflutole and its degradation products, samples were analyzed by the USGS National Water-Quality Laboratory schedule 2001 for about 52 pesticides and their degradation products.

Iowa↗
USGS2007

Concentrations of glyphosate, its degradation product, aminomethylphosphonic acid, and glufosinate in ground- and surface-water, rainfall, and soil samples collected in the United States, 2001-06

The U.S. Geological Survey conducted a number of studies from 2001 through 2006 to investigate and document the occurrence, fate, and transport of glyphosate, its degradation product, aminomethylphosphonic acid (AMPA), and glufosinate in 2,135 ground- and surface-water samples, 14 rainfall samples, and 193 soil samples. Analytical methods were developed to detect and measure glyphosate, AMPA, and glufosinate in water, rainfall, and soil. Results show that AMPA was detected more frequently and occurred at similar or higher concentrations than the parent compound, glyphosate, whereas glufosinate was seldom found in the environment. Glyphosate and AMPA were detected more frequently in surface water than in ground water. Trace levels of glyphosate and AMPA may persist in the soil from year to year. The methods and data described in this report are useful to researchers and regulators interested in the occurrence, fate, and transport of glyphosate and AMPA in the environment.

Scientific Investigations Report↗
USGS2008

Occurrence of organic compounds and trace elements in the upper Passaic and Elizabeth Rivers and their tributaries in New Jersey, July 2003 to February 2004: Phase II of the New Jersey toxics reduction workplan for New York-New Jersey Harbor

Samples of surface water and suspended sediment were collected from the Passaic and Elizabeth Rivers and their tributaries in New Jersey from July 2003 to February 2004 to determine the concentrations of selected chlorinated organic and inorganic constituents. This sampling and analysis was conducted as Phase II of the New York-New Jersey Harbor Estuary Workplan—Contaminant Assessment and Reduction Program (CARP), which is overseen by the New Jersey Department of Environmental Protection. Phase II of the New Jersey Workplan was conducted to define upstream tributary and point sources of contaminants in those rivers sampled during Phase I work, with special emphasis on the Passaic and Elizabeth Rivers. Samples were collected from three groups of tributaries: (1) the Second, Third, and Saddle Rivers; (2) the Pompton and upper Passaic Rivers; and (3) the West Branch and main stem of the Elizabeth River. The Second, Third, and Saddle Rivers were sampled near their confluence with the tidal Passaic River, but at locations not affected by tidal flooding. The Pompton and upper Passaic Rivers were sampled immediately upstream from their confluence at Two Bridges, N.J. The West Branch and the main stem of the Elizabeth River were sampled just upstream from their confluence at Hillside, N.J. All tributaries were sampled during low-flow discharge conditions using the protocols and analytical methods for organic constituents used in low-flow sampling in Phase I. Grab samples of streamflow also were collected at each site and were analyzed for trace elements (mercury, methylmercury, cadmium, and lead) and for suspended sediment, particulate organic carbon, and dissolved organic carbon. The measured concentrations and available historical suspended-sediment and stream-discharge data (where available) were used to estimate average annual loads of suspended sediment and organic compounds in these rivers. Total suspended-sediment loads for 1975–2000 were estimated using rating curves developed from historical U.S. Geological Survey (USGS) suspended-sediment and discharge data, where available. Average annual loads of suspended sediment, in millions of kilograms per year (Mkg/yr), were estimated to be 0.190 for the Second River, 0.23 for the Third River, 1.00 for the Saddle River, 1.76 for the Pompton River, and 7.40 for the upper Passaic River. On the basis of the available discharge records, the upper Passaic River was estimated to provide approximately 60 percent of the water and 80 percent of the total suspended-sediment load at the Passaic River head-of-tide, whereas the Pompton River provided roughly 20 percent of the total suspended-sediment load estimated at the head-of-tide. The combined suspended-sediment loads of the upper Passaic and Pompton Rivers (9.2 Mkg/yr), however, represent only 40 percent of the average annual suspended-sediment load estimated for the head-of-tide (23 Mkg/yr) at Little Falls, N.J. The difference between the combined suspended-sediment loads of the tributaries and the estimated load at Little Falls represents either sediment trapped upriver from the dam at Little Falls, additional inputs of suspended sediment downstream from the tributary confluence, or uncertainty in the suspended-sediment and discharge data that were used. The concentrations of total suspended sediment-bound polychlorinated biphenyls (PCBs) in the tributaries to the Passaic River were 194 ng/g (nanograms per gram) in the Second River, 575 ng/g in the Third River, 2,320 ng/g in the Saddle River, 200 ng/g in the Pompton River, and 87 ng/g in the upper Passic River. The dissolved PCB concentrations in the tributaries were 563 pg/L (picograms per liter) in the Second River, 2,510 pg/L in the Third River, 2,270 pg/L in the Saddle River, 887 pg/L in the Pompton River, and 1,000 pg/L in the upper Passaic River. Combined with the sediment loads and discharge, these concentrations resulted in annual loads of suspended sediment-bound PCBs, in grams per year (g/yr), of 37 in the Second River; 132 in the Third River; 2,320 in the Saddle River; 352 in the Pompton River; and 644 in the upper Passaic River. Annual loads of dissolved PCBs, in grams per year, are 9.2 in the Second River; 47 in the Third River; 212 in the Saddle River; 349 in the Pompton River; and 549 in the upper Passaic River. Concentrations of total suspended sediment-bound polychlorinated dibenzo-p-dioxins and polychlorinated dibenzo-p-difurans (PCDD/PCDFs) were 6,000 pg/g (picograms per gram) in the Second River; 11,300 pg/g in the Third River; 37,700 pg/g in the Saddle River; 7,140 pg/g in the Pompton River; and 9,640 pg/g in the upper Passaic River. Total toxic equivalence quotients (TEQs), which included PCDD/PCDFs and coplanar PCBs, ranged from 2.7 pg/g in the Second River to 132 pg/g (as 2,3,7,8-TCDD) in the Saddle River. Average annual loads of PCDD/PCDFs were from 1.1 g/yr in the Second River to 71 g/yr in the upper Passaic River. The load of TEQs (as 2,3,7,8-TCDD) from PCDD/PCDFs and coplanar PCBs in the tributaries were 0.5 mg/yr (milligrams per year) in the Second River, 5.8 mg/yr in the Third River, 130 mg/yr in the Saddle River, 46 mg/yr in the Pompton River, and 100 mg/yr in the upper Passaic River. These loads represent an addition to the TEQ load estimated to cross the head-of-tide of 0.1 percent by the Second River, 0.7 percent by the Third River, and 15 percent by the Saddle River. Loads of sediment-bound trace elements mercury, methylmercury, lead, and cadmium were calculated using concentrations obtained from grab samples, which were assumed to represent average annual concentrations in these rivers. Loads of sediment-bound mercury were estimated to be 1,200 g/yr in the Second River; 130 g/yr in the Third River; 4,200 g/yr in the Saddle River; 3,400 g/yr in the Pompton River; and 6,500 g/yr in the upper Passaic River. Loads of sediment-bound lead were estimated to be 56 kg/yr (kilograms per year) in the Second River; 89 kg/yr in the Third River; 1,140 kg/yr in the Saddle River; 310 kg/yr in the Pompton River; and 1,040 kg/yr in the upper Passaic River. Loads of sediment-bound cadmium were estimated to be 1 kg/yr in the Second River; 0.59 kg/yr in the Third River; 60 kg/yr in the Saddle River; 16 kg/yr in the Pompton River; and 11 kg/yr in the upper Passaic River. These loads indicate the importance of the sediment-bound contributions of organic compounds and trace elements to the upper Passaic and Saddle Rivers. Concentrations of suspended sediment-bound PCBs in the main stem and the West Branch of the Elizabeth River were 806 ng/g and 3,100 ng/g, respectively, representing loads of 40 g/yr and 1,150 g/yr, respectively. These loads were estimated using assumed discharge conditions. Concentrations of suspended sediment-bound PCDD/PCDFs were 7,270 pg/g and 9,980 pg/g in the main stem and West Branch, respectively, representing average annual loads of 0.36 g/yr and 3.7 g/yr, respectively. Total TEQ loads (sum of PCDD/PCDFs and PCBs) were 2.1 mg/yr (as 2,3,7,8-TCDD) in the main stem and 34 mg/yr in the West Branch, respectively. These load estimates, however, were directly related to the assumed annual discharge for the two branches. Long-term measurement of stream discharge and suspended-sediment concentrations would be needed to verify these loads. On the basis of the concentrations measured in this work, it appears that the West Branch is the principal source of PCBs, PCDD/PCDFs, total TEQs, and metals to the main stem of the Elizabeth River. Additional sources of these constituents may exist between the confluence and the head-of-tide.

New Jersey, New York↗
USGS2007

Summary of selected U.S. Geological survey data on domestic well water quality for the Centers for Disease Control's National Environmental Public Health Tracking Program

About 10 to 30 percent of the population in most States uses domestic (private) water supply. In many States, the total number of people served by domestic supplies can be in the millions. The water quality of domestic supplies is inconsistently regulated and generally not well characterized. The U.S. Geological Survey (USGS) has two water-quality data sets in the National Water Information System (NWIS) database that can be used to help define the water quality of domestic-water supplies: (1) data from the National Water-Quality Assessment (NAWQA) Program, and (2) USGS State data. Data from domestic wells from the NAWQA Program were collected to meet one of the Program's objectives, which was to define the water quality of major aquifers in the United States. These domestic wells were located primarily in rural areas. Water-quality conditions in these major aquifers as defined by the NAWQA data can be compared because of the consistency of the NAWQA sampling design, sampling protocols, and water-quality analyses. The NWIS database is a repository of USGS water data collected for a variety of projects; consequently, project objectives and analytical methods vary. This variability can bias statistical summaries of contaminant occurrence and concentrations; nevertheless, these data can be used to define the geographic distribution of contaminants. Maps created using NAWQA and USGS State data in NWIS can show geographic areas where contaminant concentrations may be of potential human-health concern by showing concentrations relative to human-health water-quality benchmarks. On the basis of national summaries of detection frequencies and concentrations relative to U.S. Environmental Protection Agency (USEPA) human-health benchmarks for trace elements, pesticides, and volatile organic compounds, 28 water-quality constituents were identified as contaminants of potential human-health concern. From this list, 11 contaminants were selected for summarization of water-quality data in 16 States (grantee States) that were funded by the Environmental Public Health Tracking (EPHT) Program of the Centers for Disease Control and Prevention (CDC). Only data from domestic-water supplies were used in this summary because samples from these wells are most relevant to human exposure for the targeted population. Using NAWQA data, the concentrations of the 11 contaminants were compared to USEPA human-health benchmarks. Using NAWQA and USGS State data in NWIS, the geographic distribution of the contaminants were mapped for the 16 grantee States. Radon, arsenic, manganese, nitrate, strontium, and uranium had the largest percentages of samples with concentrations greater than their human-health benchmarks. In contrast, organic compounds (pesticides and volatile organic compounds) had the lowest percentages of samples with concentrations greater than human-health benchmarks. Results of data retrievals and spatial analysis were compiled for each of the 16 States and are presented in State summaries for each State. Example summary tables, graphs, and maps based on USGS data for New Jersey are presented to illustrate how USGS water-quality and associated ancillary geospatial data can be used by the CDC to address goals and objectives of the EPHT Program.

Scientific Investigations Report↗
USGS2008

Total mercury and methylmercury in Indiana streams, August 2004-September 2006

Total mercury and methylmercury were determined by use of low (subnanogram per liter) level analytical methods in 225 representative water samples collected following ultraclean protocols at 25 Indiana monitoring stations in a statewide network, on a seasonal schedule, August 2004-September 2006. The highest unfiltered total mercury concentrations were at six monitoring stations - five that are downstream from urban and industrial wastewater discharges and that have upstream drainage areas more than 1,960 square miles and one that is downstream from active and abandoned mine lands and that has an upstream drainage area of 602 square miles. Total mercury concentrations in unfiltered samples ranged from 0.24 to 26.9 nanograms per liter (ng/L), with a median of 2.35 ng/L. The highest concentrations of total mercury, those in the 90th percentile and above, were more than 9.05 ng/L, and most were in samples collected during winter and spring 2006 during changing streamflow hydrograph conditions. Seasonal medians for unfiltered total mercury were highest during winter and spring. Instantaneous streamflow and turbidity at the time of sample collection also were highest in winter and spring and potentially indicate conditions for the most particulate mercury transport. Samples with the highest total mercury concentrations were from water that had the highest turbidity at the time of sample collection. Unfiltered total mercury concentrations were significantly lower in samples collected at five stations downstream from dams. Values for particulate total mercury and streamflow also were significantly lower at these five stations. Total mercury concentrations equaled or exceeded the 2007 Indiana chronic aquatic criterion of 12 ng/L in 5.8 percent of samples and at 10 monitoring stations. Most of the total mercury in these 13 samples was estimated to be particulate. Most of the samples with mercury concentrations that equaled or exceeded the 12 ng/L criterion were collected during winter and spring 2006 during changing streamflow hydrograph conditions and in streamflow that was high for 2004-2006. Methylmercury was detected in 83 percent of unfiltered samples; reported concentrations ranged from 0.04 to 0.57 ng/L, with a median of 0.09 ng/L. The highest concentrations of methylmercury, those in the 90th percentile and above, were more than 0.25 ng/L, and most were in samples collected during spring and summer. Methylation efficiency in most samples was less than 5.8 percent, but was as much as 24.6 percent. Seasonal medians for methylmercury were highest during spring and summer. Seasonal medians for water temperatures at the time of sample collection were highest during these seasons and potentially indicate conditions for the most formation of methylmercury. The low streamflow statistical category had the significantly highest methylation efficiency.

Indiana↗
USGS2008

Anthropogenic organic compounds in source water of nine community water systems that withdraw from streams, 2002-05

Source water, herein defined as stream water collected at a water-system intake prior to water treatment, was sampled at nine community water systems, ranging in size from a system serving about 3,000 people to one that serves about 2 million people. As many as 17 source-water samples were collected at each site over about a 12-month period between 2002 and 2004 for analysis of 258 anthropogenic organic compounds. Most of these compounds are unregulated in drinking water, and the compounds analyzed include pesticides and selected pesticide degradates, gasoline hydrocarbons, personal-care and domestic-use compounds, and solvents. The laboratory analytical methods used in this study have relatively low detection levels - commonly 100 to 1,000 times lower than State and Federal standards and guidelines for protecting water quality. Detections, therefore, do not necessarily indicate a concern to human health but rather help to identify emerging issues and to track changes in occurrence and concentrations over time. About one-half (134) of the compounds were detected at least once in source-water samples. Forty-seven compounds were detected commonly (in 10 percent or more of the samples), and six compounds (chloroform, atrazine, simazine, metolachlor, deethylatrazine, and hexahydrohexamethylcyclopentabenzopyran (HHCB) were detected in more than one-half of the samples. Chloroform was the most commonly detected compound - in every sample (year round) at five sites. Findings for chloroform and the fragrances HHCB and acetyl hexamethyl tetrahydronaphthalene (AHTN) indicate an association between occurrence and the presence of large upstream wastewater discharges in the watersheds. The herbicides atrazine, simazine, and metolachlor also were among the most commonly detected compounds. Degradates of these herbicides, as well as those of a few other commonly occurring herbicides, generally were detected at concentrations similar to or greater than concentrations of the parent compound. Samples typically contained mixtures of two or more compounds. The total number of compounds and their total concentration in samples generally increased with the amount of urban and agricultural land use in a watershed. Annual mean concentrations of all compounds were less than human-health benchmarks. Single-sample concentrations of anthropogenic organic compounds in source water generally were less than 0.1 microgram per liter and less than established human-health benchmarks. Human-health benchmarks used for comparison were U.S. Environmental Protection Agency (USEPA) Maximum Contaminant Levels (MCLs) for regulated compounds and U.S. Geological Survey Health-Based Screening Levels for unregulated compounds. About one-half of all detected compounds do not have human-health benchmarks or adequate toxicity information for evaluating results in a human-health context. During a second sampling phase (2004-05), source water and finished water (water that has passed through all the treatment processes but prior to distribution) were sampled at eight of the nine community water systems. Water-treatment processes differ among the systems. Specifically, treatment at five of the systems is conventional, typically including steps of coagulation, flocculation, sedimentation, filtration, and disinfection. One water system uses slow sand filtration and disinfection, a second system uses ozone as a preliminary treatment step to conventional treatment, and a third system is a direct filtration treatment plant that uses many of the steps employed in conventional treatment. Most of these treatment steps are not designed specifically to remove the compounds monitored in this study. About two-thirds of the compounds detected commonly in source water were detected at similar frequencies in finished water. Although the water-treatment steps differ somewhat among the eight water systems, the amount of change in concentration of the compounds from source- to finish

Scientific Investigations Report↗
USGS2009

Factors affecting water quality in selected carbonate aquifers in the United States, 1993-2005

Carbonate aquifers are an important source of water in the United States; however, these aquifers can be particularly susceptible to contamination from the land surface. The U.S. Geological Survey National Water-Quality Assessment (NAWQA) Program collected samples from wells and springs in 12 carbonate aquifers across the country during 1993–2005; water-quality results for 1,042 samples were available to assess the factors affecting ground-water quality. These aquifers represent a wide range of climate, land-use types, degrees of confinement, and other characteristics that were compared and evaluated to assess the effect of those factors on water quality. Differences and similarities among the aquifers were also identified. Samples were analyzed for major ions, radon, nutrients, 47 pesticides, and 54 volatile organic compounds (VOCs). Geochemical analysis helped to identify dominant processes that may contribute to the differences in aquifer susceptibility to anthropogenic contamination. Differences in concentrations of dissolved oxygen and dissolved organic carbon and in ground-water age were directly related to the occurrence of anthropogenic contaminants. Other geochemical indicators, such as mineral saturation indexes and calcium-magnesium molar ratio, were used to infer residence time, an indirect indicator of potential for anthropogenic contamination. Radon exceeded the U.S. Environmental Protection Agency proposed Maximum Contaminant Level (MCL) of 300 picocuries per liter in 423 of 735 wells sampled, of which 309 were drinking-water wells. In general, land use, oxidation-reduction (redox) status, and degree of aquifer confinement were the most important factors affecting the occurrence of anthropogenic contaminants. Although none of these factors individually accounts for all the variation in water quality among the aquifers, a combination of these characteristics accounts for the majority of the variation. Unconfined carbonate aquifers that had high percentages of urban or agricultural land, or a combination of both, had higher concentrations and higher frequency of detections for most of the anthropogenic contaminants than areas with other combinations of land use and degree of aquifer confinement. Redox status is an indicator of more recently recharged water and affects the fate of some contaminants. Median concentrations of nitrate were highest in the Valley and Ridge and Piedmont aquifers and lowest in the Biscayne and Silurian-Devonian/Upper carbonate aquifers. Nitrate concentrations were significantly higher in unconfined aquifers than in confined aquifers and semiconfined/mixed confined aquifers (wells in aquifers with breached confining layers or wells open to both a confined and an unconfined aquifer). Water recharged after 1953 had significantly higher concentrations of nitrate than water recharged prior to 1953. Redox status was also a key factor affecting nitrate concentrations; in recently recharged waters, samples in oxic waters had significantly higher concentrations of nitrate than anoxic waters, regardless of land use in the area around the well. Samples from 54 wells (5 percent) exceeded the U.S. Environmental Protection Agency MCL of 10 mg/L for nitrate in drinking water. Most of the samples exceeding the drinking-water standard (52 samples, or 5 percent) were in domestic supply wells in agricultural areas. The Piedmont and Valley and Ridge aquifers had the largest number of samples (45) exceeding the MCL; in the remaining aquifers only 9 samples had concentrations of nitrate that exceeded the MCL (about 1 percent). None of the water recharged prior to 1953 and only a single sample from a confined aquifer had nitrate concentrations that exceeded 10 mg/L as N. Wells were sampled for a minimum of 47 pesticides. Detection frequencies and comparisons varied depending on the assessment level used. At least 1 of the 47 pesticides was detected at 510 (50 percent) of the 1,027 sites where pesticide data were available using the ‘all detections’ assessment level—that is, including any quantified detection as well as any estimated values where the compound was definitively detected. Multiple pesticides were frequently detected in a sample of water from a site; 34 percent of the samples had two to five pesticides detected in the same sample, and 4 percent of the samples had six or more pesticides detected. Dieldrin was detected at 20 sites, 9 of which were from either domestic or public supply wells, at a concentration above the Health-Based Screening Level (HBSL) of 0.002 µg/L. Diazinon was detected at a concentration greater than the HBSL of 1 µg/L at a single site, which was also a domestic supply well. These are the only samples where a pesticide exceeded a human-health benchmark. The most frequently occurring pesticide compounds were four herbicides—atrazine, simazine, metolachlor, and prometon—and deethylatrazine, a degradate of atrazine. These pesticides typically were detected at concentrations that were less than 10 percent of a human-health benchmark. Of the four frequently occurring pesticides, only samples for atrazine (3 percent) and simazine (0.1 percent) had concentrations that exceeded 10 percent of the human-health benchmark; most of these cases were in agricultural areas. It is important to note, however, that the most frequently occurring pesticide degradate compound—deethylatrazine—has no human-health benchmark. Using a common assessment level of 0.01 µg/L, four of the aquifers—Biscayne, Mississippian, Piedmont, and Valley and Ridge—had at least one of these five compounds detected in more than 30 percent of the wells sampled. These four aquifers, along with the Ordovician, Ozark Plateaus, and Prairie du Chien aquifers were the aquifers or aquifer systems that had concentrations of pesticides that exceeded 10 percent of a human-health benchmark. Water recharged after 1953 had a significantly higher percentage of detections of pesticides than water recharged before 1953, and water from unconfined aquifers had a significantly higher percentage of detections of pesticides than water from confined or semiconfined/mixed confined aquifers. Water from sites in unconfined aquifers, where land use was agricultural or urban, accounted for the vast majority of detections of pesticides. Dissolved oxygen concentration was positively related to pesticide occurrence, which likely reflects the positive association between dissolved oxygen concentration and recently recharged water. Water samples were collected for analysis of VOCs at 793 sites—154 samples were analyzed for 54 VOCs from 1993 through 1995 and 639 samples were analyzed for 86 VOCs from 1996 through 2005. Twenty percent of samples contained one or more VOCs at concentrations greater than or equal to 0.2 µg/L (159 of 793 samples). The aquifers with the highest percentage of samples containing one or more VOCs were the Castle Hayne (about 41 percent of samples) and Biscayne aquifers (34 percent). The most frequently detected VOCs were chloroform, tetrahydrofuran, tetrachloroethene (PCE), toluene, acetone, ethylmethylketone, methyl tert-butyl ether (MTBE), and trichloroethene (TCE). Low-level concentrations of VOCs occurred in a much larger percentage of a subset of the data (the 639 samples analyzed using a low-level analytical method). In these samples, 69 percent of the 639 samples contained 1 or more VOCs, indicating the vulnerability of the carbonate aquifers to low-level VOC contamination. Four VOCs were detected at concentrations exceeding their respective MCLs in five samples, all of which were from drinking-water wells. Vinyl chloride concentrations exceeded the MCL of 2 µg/L in two samples from urban areas in the unconfined Biscayne aquifer. PCE, TCE, and 1,2-dichloropropane each had one sample with a concentration greater than their MCLs of 5 µg/L; these samples were from agricultural and urban areas in the unconfined Mississippian aquifer. Water quality in the 12 carbonate aquifers was highly variable. Most of the samples met drinking-water standards. The occurrence of anthropogenic contaminants was related to contaminant sources but also was affected by degree of aquifer confinement, ground-water age, and redox status. Areas with higher amounts of agricultural or urban land in unconfined aquifers were the most likely to have elevated concentrations of anthropogenic contaminants.

Scientific Investigations Report↗
USGS2009

Sources and preparation of data for assessing trends in concentrations of pesticides in streams of the United States, 1992-2006

This report provides a water-quality data set of 44 commonly used pesticides and 8 pesticide degradates suitable for a national assessment of trends in pesticide concentrations in streams of the United States. Water-quality samples collected from January 1992 through August 2006 at stream-water sites of the U.S. Geological Survey National Water-Quality Assessment Program and the National Stream Quality Accounting Network Program were compiled, reviewed, selected, and prepared for trend analysis as described in this report. Samples analyzed at the U.S. Geological Survey National Water Quality Laboratory by a gas chromatography/mass spectrometry analytical method were the most extensive in time and space and were selected for national trend analysis. The selection criteria described in the report produced a trend data set of 16,869 pesticide samples at 201 stream and river sites.

Scientific Investigations Report↗
USGS2009

Development and Evaluation of Live-Bed Pier- and Contraction-Scour Envelope Curves in the Coastal Plain and Piedmont Provinces of South Carolina

The U.S. Geological Survey, in cooperation with the South Carolina Department of Transportation, used ground-penetrating radar to collect measurements of live-bed pier scour and contraction scour at 78 bridges in the Piedmont and Coastal Plain Physiographic Provinces of South Carolina. The 151 measurements of live-bed pier-scour depth ranged from 1.7 to 16.9 feet, and the 89 measurements of live-bed contraction-scour depth ranged from 0 to 17.1 feet. Using hydraulic data estimated with a one-dimensional flow model, predicted live-bed scour depths were computed with scour equations from the Hydraulic Engineering Circular 18 and compared with measured scour. This comparison indicated that predicted pier-scour depths generally exceeded the measured pier-scour depths, and at times predicted pier-scour depths were excessive (overpredictions were as large as 23.1 feet). For live-bed contraction-scour depths, predicted scour was sometimes excessive (overpredictions were as large as 14.3 feet), but often observed contraction scour was underpredicted. For live-bed pier scour, trends in laboratory and field data were compared and found to be similar. The strongest explanatory variable was pier width, and an envelope curve for assessing the upper bound of live-bed pier scour was developed using pier width as the primary explanatory variable. Relations in the live-bed contraction-scour data also were investigated, and several envelope curves were developed using the geometric-contraction ratio as the primary explanatory variable. The envelope curves developed with the field data have limitations, but the envelope curves can be used as supplementary tools for assessing the potential for live-bed pier and contraction scour in South Carolina. Data from this study were compiled into a database that includes photographs, measured scour depths, predicted scour depths, limited basin characteristics, limited soil data, and modeled hydraulic data. The South Carolina database can be used in the comparison of sites with similar characteristics to evaluate the potential for scour. In addition, the database can be used to evaluate the performance of various analytical methods for predicting live-bed pier and contraction scour.

South Carolina↗
USGS2009

Evaluation of passive samplers for long-term monitoring of organic compounds in the untreated drinking water supply for the city of Eugene, Oregon, September–October 2007

Two types of passive samplers, polar organic chemical integrative samplers (POCIS) and semipermeable membrane devices (SPMDs), were deployed at three sites in the McKenzie River basin during September-October 2007. The McKenzie River is the source of drinking water for the city of Eugene, Oregon, and the work presented here was designed to evaluate the use of POCIS and SMPDs as part of a long-term monitoring plan for the river. Various compounds were detected in extracts from the POCIS and SPMDs, indicating that some compounds of concern are present in the McKenzie River basin, including the intake for the drinking water plant. However, most concentrations were near the quantitation limits of the analytical methods used - generally at subnanogram per liter concentrations - and would not have been detectable with conventional water sampling and analysis methods. These results indicate that both POCIS and SPMDs are well suited to monitor organic compounds in the McKenzie River basin.

Oregon↗
USGS2009

Anthropogenic organic compounds in source water of selected community water systems that use groundwater, 2002-05

Source water, defined as groundwater collected from a community water system well prior to water treatment, was sampled from 221 wells during October 2002 to July 2005 and analyzed for 258 anthropogenic organic compounds. Most of these compounds are unregulated in drinking water and include pesticides and pesticide degradates, gasoline hydrocarbons, personal-care and domestic-use products, and solvents. The laboratory analytical methods used in the study have detection levels that commonly are 100 to 1,000 times lower than State and Federal standards and guidelines for protecting water quality. Detections of anthropogenic organic compounds do not necessarily indicate a concern to human health but rather help to identify emerging issues and track changes in occurrence and concentrations over time. Less than one-half (120) of the 258 compounds were detected in at least one source-water sample. Chloroform, in 36 percent of samples, was the most commonly detected of the 12 compounds that were in about 10 percent or more of source-water samples. The herbicides atrazine, metolachlor, prometon, and simazine also were among the commonly detected compounds. The commonly detected degradates of atrazine - deethylatrazine and deisopropylatrazine - as well as degradates of acetochlor and alachlor, generally were detected at concentrations similar to or greater than concentrations of the parent herbicide. The compounds perchloroethene, trichloroethene, 1,1,1-trichloroethane, methyl tert-butyl ether, and cis-1,2-dichloroethene also were detected commonly. The most commonly detected compounds in source-water samples generally were among those detected commonly across the country and reported in previous studies by the U.S. Geological Survey's National Water-Quality Assessment Program. Relatively few compounds were detected at concentrations greater than human-health benchmarks, and 84 percent of the concentrations were two or more orders of magnitude less than benchmarks. Five compounds (perchloroethene, trichloroethene, 1,2-dibromoethane, acrylonitrile, and dieldrin) were detected at concentrations greater than their human-health benchmark. The human-health benchmarks used for comparison were U.S. Environmental Protection Agency Maximum Contaminant Levels (MCLs) for regulated compounds and Health-Based Screening Levels developed by the U.S. Geological Survey in collaboration with the U.S. Environmental Protection Agency and other agencies for unregulated compounds. About one-half of all detected compounds do not have human-health benchmarks or adequate toxicity information to evaluate results in a human-health context. Ninety-four source-water and finished-water (water that has passed through all the treatment processes but prior to distribution) sites were sampled at selected community water systems during June 2004 to September 2005. Most of the samples were analyzed for compounds that were detected commonly or at relatively high concentrations during the initial source-water sampling. The majority of the finished-water samples represented water blended with water from one or more other wells. Thirty-four samples were from water systems that did not blend water from sampled wells with water from other wells prior to distribution. The comparison of source- and finished-water samples represents an initial assessment of whether compounds present in source water also are present in finished water and is not intended as an evaluation of water-treatment efficacy. The treatment used at the majority of the community water systems sampled is disinfection, which, in general, is not designed to remove the compounds monitored in this study. Concentrations of all compounds detected in finished water were less than their human-health benchmarks. Two detections of perchloroethene and one detection of trichloroethene in finished water had concentrations within an order of magnitude of the MCL. Concentrations of disinfection by-products were

Scientific Investigations Report↗
USGS2010

Organic compounds and cadmium in the tributaries to the Elizabeth River in New Jersey, October 2008 to November 2008: Phase II of the New Jersey Toxics Reduction Workplan for New York-New Jersey Harbor

Samples of surface water and suspended sediment were collected from the two branches that make up the Elizabeth River in New Jersey - the West Branch and the Main Stem - from October to November 2008 to determine the concentrations of selected chlorinated organic and inorganic constituents. The sampling and analyses were conducted as part of Phase II of the New York-New Jersey Harbor Estuary Plan-Contaminant Assessment and Reduction Program (CARP), which is overseen by the New Jersey Department of Environmental Protection. Phase II of the New Jersey Workplan was conducted by the U.S. Geological Survey to define upstream tributary and point sources of contaminants in those rivers sampled during Phase I work, with special emphasis on the Passaic and Elizabeth Rivers. This portion of the Phase II study was conducted on the two branches of the Elizabeth River, which were previously sampled during July and August of 2003 at low-flow conditions. Samples were collected during 2008 from the West Branch and Main Stem of the Elizabeth River just upstream from their confluence at Hillside, N.J. Both tributaries were sampled once during low-flow discharge conditions and once during high-flow discharge conditions using the protocols and analytical methods that were used in the initial part of Phase II of the Workplan. Grab samples of streamwater also were collected at each site and were analyzed for cadmium, suspended sediment, and particulate organic carbon. The measured concentrations, along with available historical suspended-sediment and stream-discharge data were used to estimate average annual loads of suspended sediment and organic compounds in the two branches of the Elizabeth River. Total suspended-sediment loads for 1975 to 2000 were estimated using rating curves developed from historical U.S. Geological Survey suspended-sediment and discharge data, where available. Concentrations of suspended-sediment-bound polychlorinated biphenyls (PCBs) in the Main Stem and the West Branch of the Elizabeth River during low-flow conditions were 534 ng/g (nanograms per gram) and 1,120 ng/g, respectively, representing loads of 27 g/yr (grams per year) and 416 g/yr, respectively. These loads were estimated using contaminant concentrations during low flow, and the assumed 25-year average discharge, and 25-year average suspended-sediment concentration. Concentrations of suspended-sediment-bound PCBs in the Main Stem and the West Branch of the Elizabeth River during high-flow conditions were 3,530 ng/g and 623 ng/g, respectively, representing loads of 176 g/yr and 231 g/yr, respectively. These loads were estimated using contaminant concentrations during high-flow conditions, the assumed 25-year average discharge, and 25-year average suspended-sediment concentration. Concentrations of suspended-sediment-bound polychlorinated dibenzo-p-dioxins and polychlorinated dibenzo-p-difuran compounds (PCDD/PCDFs) during low-flow conditions were 2,880 pg/g (picograms per gram) and 5,910 pg/g in the Main Stem and West Branch, respectively, representing average annual loads of 0.14 g/yr and 2.2 g/yr, respectively. Concentrations of suspended-sediment-bound PCDD/PCDFs during high-flow conditions were 40,900 pg/g and 12,400 pg/g in the Main Stem and West Branch, respectively, representing average annual loads of 2.05 g/yr and 4.6 g/yr, respectively. Total toxic equivalency (TEQ) loads (sum of PCDD/PCDF and PCB TEQs) were 3.1 mg/yr (milligrams per year) (as 2, 3, 7, 8-TCDD) in the Main Stem and 28 mg/yr in the West Branch during low-flow conditions. Total TEQ loads (sum of PCDD/PCDFs and PCBs) were 27 mg/yr (as 2, 3, 7, 8-TCDD) in the Main Stem and 32 mg/yr in the West Branch during high-flow conditions. All of these load estimates, however, are directly related to the assumed annual discharge for the two branches. Long-term measurement of stream discharge and suspended-sediment concentrations would be needed to verify these loads. On the basis of the loads cal

Scientific Investigations Report↗