Search USGS⌕ Search

SEARCH · Search USGS

Results for “Polycyclic Aromatic Compounds”

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 55 records · Page 3Linked to original sources
USGS2012

Establishment of sentinel sampling sites to monitor changes in water and sediment quality and biota related to visitor use at Lake Powell, Arizona and Utah, 2004-2006

Twenty sentinel sampling sites were established and sampled during 2004–06 at Lake Powell, Arizona and Utah, by the U.S. Geological Survey and the National Park Service—Glen Canyon National Recreation Area. The sentinel sampling sites provide sampling locations on Lake Powell, the Nation’s second largest reservoir that can be visited and sampled repeatedly over time to monitor changes in water and sediment quality and also biota. The sites were established in response to an Environmental Impact Statement that addressed the use of personal watercraft on Lake Powell. The use of personal watercraft can potentially introduce hydrocarbons and other contaminants and are of concern to the health of visitors and aquatic habitats of these environments. Data from this initial sampling period (2004–06) include (1) discrete measurements of water temperature, specific conductance, pH, and water clarity; (2) major ions, nutrients, and organic carbon; (3) trace elements including rare earths; (4) organic compounds including oil and grease, total petroleum hydrocarbons, and volatile organic compounds; (5) polycyclic aromatic hydrocarbons in lakebed sediments; and (6) continuous depth profile measurements of water temperature, specific conductance, pH, dissolved oxygen, and turbidity. Also, the National Park Service-Glen Canyon National Recreation Area collected bacteria samples during this initial sampling period.

Arizona;Utah↗
USGS2004

Chemical Data for Detailed Studies of Irrigation Drainage in the Salton Sea Area, California, 1995?2001

The primary purpose of this report is to present all chemical data from the Salton Sea area collected by the U.S. Geological Survey between 1995 and 2001. The data were collected primarily for the Department of the Interior's National Irrigation Water Quality Program (NIWQP). The report also contains a brief summary and citation to investigations done for the NIWQP between 1992 and 1995. The NIWQP began studies in the Salton Sea area in 1986 to evaluate effects on the environment from potential toxins, especially selenium, in irrigation-induced drainage. This data report is a companion to several reports published from the earlier studies and to interpretive publications that make use of historical and recent data from this area. Data reported herein are from five collection studies. Water, bottom material, and suspended sediment collected in 1995-96 from the New River, the lower Colorado River, and the All-American Canal were analyzed for elements, semi-volatile (extractable) organic compounds, and organochlorine compounds. Sufficient suspended sediment for chemical analyses was obtained by tangential-flow filtration. A grab sample of surficial bottom sediment collected from near the deepest part of the Salton Sea in 1996 was analyzed for 44 elements and organic and inorganic carbon. High selenium concentration confirmed the effective transfer (sequestration) of selenium into the bottom sediment. Similar grab samples were collected 2 years later (1998) from 11 locations in the Salton Sea and analyzed for elements, as before, and also for nutrients, organochlorine compounds, and polycyclic aromatic hydrocarbons. Nutrients were measured in bottom water, and water-column profiles were obtained for pH, conductance, temperature, and dissolved oxygen. Element and nutrient concentrations were obtained in 1999 from cores at 2 of the above 11 sites, in the north subbasin of the Salton Sea. The most-recent study reported herein was done in 2001 and contains element data on suspended material isolated by continuous-flow centrifugation on samples collected in transects extending out from the Whitewater, the Alamo, and the New Rivers into the Salton Sea. Chemical data on suspended sediment and bottom material from tributory rivers and the Salton Sea itself show that many insoluble constituents, including selenium and DDE, are concentrated in the fine-grained, organic- and carbonate-rich bottom sediment from deep areas near the center of the Salton Sea. Data also show that selenium and arsenic are markedly enriched in seston (plankton, partially-degraded algal detritus, and mineral matter that compose suspended particulates in the lake) collected just below the water surface in the Salton Sea. This result indicates that bio-concentration in primary producers in the water column provides an important pathway whereby high selenium residues accumulate in fish and fish-eating birds at the Salton Sea.

Scientific Investigations Report↗
USGS2008

Hydrologic and Water-Quality Responses in Shallow Ground Water Receiving Stormwater Runoff and Potential Transport of Contaminants to Lake Tahoe, California and Nevada, 2005-07

Clarity of Lake Tahoe, California and Nevada has been decreasing due to inflows of sediment and nutrients associated with stormwater runoff. Detention basins are considered effective best management practices for mitigation of suspended sediment and nutrients associated with runoff, but effects of infiltrated stormwater on shallow ground water are not known. This report documents 2005-07 hydrogeologic conditions in a shallow aquifer and associated interactions between a stormwater-control system with nearby Lake Tahoe. Selected chemical qualities of stormwater, bottom sediment from a stormwater detention basin, ground water, and nearshore lake and interstitial water are characterized and coupled with results of a three-dimensional, finite-difference, mathematical model to evaluate responses of ground-water flow to stormwater-runoff accumulation in the stormwater-control system. The results of the ground-water flow model indicate mean ground-water discharge of 256 acre feet per year, contributing 27 pounds of phosphorus and 765 pounds of nitrogen to Lake Tahoe within the modeled area. Only 0.24 percent of this volume and nutrient load is attributed to stormwater infiltration from the detention basin. Settling of suspended nutrients and sediment, biological assimilation of dissolved nutrients, and sorption and detention of chemicals of potential concern in bottom sediment are the primary stormwater treatments achieved by the detention basins. Mean concentrations of unfiltered nitrogen and phosphorus in inflow stormwater samples compared to outflow samples show that 55 percent of nitrogen and 47 percent of phosphorus are trapped by the detention basin. Organic carbon, cadmium, copper, lead, mercury, nickel, phosphorus, and zinc in the uppermost 0.2 foot of bottom sediment from the detention basin were all at least twice as concentrated compared to sediment collected from 1.5 feet deeper. Similarly, concentrations of 28 polycyclic aromatic hydrocarbon compounds were all less than laboratory reporting limits in the deeper sediment sample, but 15 compounds were detected in the uppermost 0.2 foot of sediment. Published concentrations determined to affect benthic aquatic life also were exceeded for copper, zinc, benz[a]anthracene, phenanthrene, and pyrene in the shallow sediment sample. Isotopic composition of water (oxygen 18/16 and hydrogen 2/1 ratios) for samples of shallow ground water, lakewater, and interstitial water from Lake Tahoe indicate the lake was well mixed with a slight ground-water signature in samples collected near the lakebed. One interstitial sample from 0.8 foot beneath the lakebed was nearly all ground water and concentrations of nitrogen and phosphorus were comparable to concentrations in shallow ground-water samples. However, ammonium represented 65 percent of filtered nitrogen in this interstitial sample, but only 10 percent of the average nitrogen in ground-water samples. Nitrate was less than reporting limits in interstitial water, compared with mean nitrate concentration of 750 micrograms per liter in ground-water samples, indicating either active dissimilative nitrate reduction to ammonium by micro-organisms or hydrolysis of organic nitrogen to ammonium with concomitant nitrate reduction. The other interstitial sample falls along a mixing line between ground water and lake water and most of the nitrogen was organic nitrogen.

Scientific Investigations Report↗
USGS2015

Trace-metal and organic constituent concentrations in bed sediment at Big Base and Little Base Lakes, Little Rock Air Force Base, Arkansas—Comparisons to sediment-quality guidelines and indications for timing of exposure

This report compares concentrations for a wide range of inorganic and organic constituents in bed sediment from Big Base Lake and Little Base Lake, which are located on Little Rock Air Force Base, Arkansas, to sediment-quality guidelines. This report also compares trace-metal concentrations in a bed-sediment core sample to sediment age to determine when the highest concentrations of trace metals were deposited in Big Base Lake. Trace-metal results often were higher than background concentrations in the surrounding Pulaski County area, and concentrations of arsenic, cadmium, cobalt, copper, lead, manganese, mercury, nickel, and zinc at one or more of three study sites were higher than median concentrations for a study involving 98 urban streams in seven metropolitan areas of the United States. Concentrations for most polycyclic aromatic hydrocarbons, polychlorinated biphenyls, and organochlorine pesticides in all three bed-sediment samples were less than the laboratory reporting limit or were detected at low concentrations. Some contaminants were detected at concentrations that are potentially toxic to sediment-dwelling biota; however, in general, the analyses suggest that the risk of sediment toxicity may be relatively low. Threshold effect concentrations were exceeded for 14 constituents—arsenic, copper, lead, nickel, and zinc, five polycyclic aromatic hydrocarbons compounds, chlordane, and all three dichlorodiphenyltrichloroethane (DDT) congeners—which suggests potential toxicity to some sediment-dwelling biota. Only two constituents had concentrations that exceeded published probable effect concentrations—arsenic (at the deepest site in Big Base Lake, NS6) and p,p’-dichlorodiphenyldichloroethylene (p,p’-DDE; at both sites in Big Base Lake, NS5 and NS6). Regarding highest concentrations and associated timing of exposure, trace metals analyzed in the sediment core seem to indicate three fairly distinct exposure patterns. For 11 trace metals that had the highest concentration measured in the shallowest and most recently deposited sediment, the most likely explanation is recent exposure by anthropogenic activities. Most of the 11 trace metals with highest concentrations in shallow sediment are relatively innocuous; however, arsenic, copper, selenium, and zinc are among the U.S. Environmental Protection Agency’s 126 priority pollutants. For three trace metals (cadmium, lead, and mercury), for which concentrations were highest in sediments that were 16–20 centimeters down the core, it is likely that a source associated with those contaminants during the period when those sediments were deposited, was reduced or eliminated. The eight remaining trace metals, for which concentrations were highest in sediments that were just below the prereservoir surface, likely had sources that were eliminated soon after lake construction or occurred at relatively high background concentrations in soils in the area around Little Rock Air Force Base.

Arkansas↗
USGS2010

Sediment contamination of residential streams in the metropolitan Kansas City area, USA: Part I. distribution of polycyclic aromatic hydrocarbon and pesticide-related compounds

This is the first part of a study that evaluates the influence of nonpoint-source contaminants on the sediment quality of five streams within the metropolitan Kansas City area, central United States. Surficial sediment was collected in 2003 from 29 sites along five streams with watersheds that extend from the core of the metropolitan area to its development fringe. Sediment was analyzed for 16 polycyclic aromatic hydrocarbons (PAHs), 3 common polychlorinated biphenyl mixtures (Aroclors), and 25 pesticide-related compounds of eight chemical classes. Multiple PAHs were detected at more than 50% of the sites, and concentrations of total PAHs ranged from 290 to 82,150 μg/kg (dry weight). The concentration and frequency of detection of PAHs increased with increasing urbanization of the residential watersheds. Four- and five-ring PAH compounds predominated the PAH composition (73–100%), especially fluoranthene and pyrene. The PAH composition profiles along with the diagnostic isomer ratios [e.g., anthracene/(anthracene + phenanthrene), 0.16 ± 0.03; fluoranthene/(fluoranthene + pyrene), 0.55 ± 0.01)] indicate that pyrogenic sources (i.e., coal-tar-related operations or materials and traffic-related particles) may be common PAH contributors to these residential streams. Historical-use organochlorine insecticides and their degradates dominated the occurrences of pesticide-related compounds, with chlordane and dieldrin detected in over or nearly 50% of the samples. The occurrence of these historical organic compounds was associated with past urban applications, which may continue to be nonpoint sources replenishing local streams. Concentrations of low molecular weight (LMW; two or three rings) and high molecular weight (HMW; four to six rings) PAHs covaried along individual streams but showed dissimilar distribution patterns between the streams, while the historical pesticide-related compounds generally increased in concentration downstream. Correlations were noted between LMW and HMW PAHs for most of the streams and between historical-use organochlorine compounds and total organic carbon and clay content of sediments for one of the streams (Brush Creek). Stormwater runoff transport modes are proposed to describe how the two groups of contaminants migrated and distributed in the streambed.

Kansas, Missouri↗
USGS2010

A Reconnaissance of selected organic compounds in streams in tribal lands in Central Oklahoma, January-February 2009

The U.S. Geological Survey worked in cooperation with the U.S. Environmental Protection Agency and the Kickapoo Tribe of Oklahoma on two separate reconnaissance projects carried out concurrently. Both projects entailed the use of passive samplers as a sampling methodology to investigate the detection of selected organic compounds at stream sites in jurisdictional areas of several tribes in central Oklahoma during January-February 2009. The focus of the project with the U.S. Environmental Protection Agency was the detection of pesticides and pesticide metabolites using Semipermeable Membrane Devices at five stream sites in jurisdictional areas of several tribes. The project with the Kickapoo Tribe of Oklahoma focused on the detection of pesticides, pesticide metabolites, polycyclic aromatic hydrocarbons, polychlorinated biphenyl compounds, and synthetic organic compounds using Semipermeable Membrane Devices and Polar Organic Chemical Integrative Samplers at two stream sites adjacent to the Kickapoo tribal lands. The seven stream sites were located in central Oklahoma on the Cimarron River, Little River, North Canadian River, Deep Fork, and Washita River. Extracts from SPMDs submerged at five stream sites, in cooperation with the U.S. Environmental Protection Agency, were analyzed for 46 pesticides and 6 pesticide metabolites. Dacthal, a pre-emergent herbicide, was detected at all five sites. Pendimethalin, also a pre-emergent, was detected at one site. The insecticides chlorpyrifos and dieldrin were detected at three sites and p,p'-DDE, a metabolite of the insecticide DDT, also was detected at three sites. SPMDs and POCIS were submerged at the upstream edge and downstream edge of the Kickapoo tribal boundaries. Both sites are downstream from the Oklahoma City metropolitan area and multiple municipal wastewater treatment plants. Extracts from the passive samplers were analyzed for 62 pesticides, 10 pesticide metabolites, 3 polychlorinated biphenyl compounds, 35 polycyclic aromatic hydrocarbons, and 49 synthetic organic compounds. Ten pesticides and four pesticide metabolites were detected at the upstream site and seven pesticides and four pesticide metabolites were detected at the downstream site. Pesticides detected at both sites were atrazine, chlorpyrifos, dacthal, dieldrin, metolachlor, pendimethalin, and trans-nonachlor. Additionally at the upstream site, heptachlor, pentachlorophenol, and prometon were detected. The pesticide metabolites p,p'-DDE, cis-chlordane, and trans-chlordane also were detected at both sites. Polychlorinated biphenyl compounds aroclor-1016/1242, aroclor-1254, and aroclor-1260 were detected at both sites. The upstream site had 16 polycyclic aromatic hydrocarbon detections and the downstream site had 8 detections. Because of chromatographic interference during analysis, a positive identification of 17 polycyclic aromatic hydrocarbons could not be made. Consequently, there may have been a greater number of these compounds detected at both sites. A total of 36 synthetic organic compounds were detected at the two sites adjacent to the Kickapoo tribal lands. The upstream site had 21 synthetic organic compound detections: three detergent metabolites, two fecal indicators, three flame retardants, seven industrial compounds, five compounds related to personal care products, and beta-sitosterol, a plant sterol. Fifteen synthetic organic compounds were detected at the downstream site and included: one fecal indicator, three flame retardants, six industrial compounds, and five compounds related to personal care products.

Scientific Investigations Report↗
USGS1995

Water-quality characteristics of selected public recreational lakes and ponds in Connecticut

Reconnaissance limnological and lakebed-sediment surveys were conducted in Connecticut during 1989-91 by the U.S. Geological Survey, in cooperation with the Connecticut Department of Environmental Protec- tion, to evaluate water-quality characteristics of selected public recreational lakes and ponds in the State. Limnological surveys were conducted on 49 lakes and ponds selected from a list of 105 publicly owned waterbodies that qualified for water- quality assessments under Section 314 of the Federal Clean Water Act. Lakebed-sediment surveys were conducted in 9 river impoundments and 1 riverine lake below industrial areas and 2 headwater lakes in relatively pristine areas. The limnological surveys consisted of two sampling events--during spring turnover and during the summer stratifi- cation. Each sampling event included depth profiles of water temperature, specific conductance, hydrogen-ion activity, and dissolved oxygen concen- trations; measurements of Secchi disc transparency; and the collection of samples for the analyses of alkalinity, chlorophyll, phosphorus, and nitrogen concentrations. Areal extent and population density of the dominant aquatic macrophytes were qualita- tively noted during the summer sampling event. These water-quality data were used to determine the trophic classification and acidification status of the 49 lakes. The trophic classification yielded the following results: 2 oligotrophic, 8 early mesotrophic, 13 mesotrophic, 5 late mesotrophic, 10 eutrophic, and 11 highly eutrophic lakes. In terms of acidification status, 7 lakes were classified as acid threatened and 42 as not threatened. A Wilcoxon two-tailed signed rank test was used to compare data for 13 lakes and ponds from the present survey with data from the 1973-75 or 1978-79 surveys conducted by the Connecticut Agricultural Experiment Station and Connecticut Department of Environmental Protection. The test showed no significant difference at the 90 percent confidence level for spring nitrogen and summer chlorophyll-a concen- trations, a significant increase at the 90 percent confidence level in summer phosphorus concentra- tions, and a significant decrease at the 95 percent confidence level in summer transparency. For the lakebed-sediment surveys, composite-grab samples were collected from the deepest part of each lake. Samples were analyzed for arsenic, cyanide, organic and inorganic carbon, selected metals, and methylene-extractable, synthetic organic compounds classified by the U.S. Environmental Protection Agency as semi-volatile priority pollutants. Hanover Pond, Eagleville Lake, and West Thompson Lake had three of the four highest concentrations of cadmium, chromium, copper, lead, nickel, zinc, and cyanide. The four lakes with the highest concentrations of arsenic (Aspinook Pond, Fitchville Pond, Mashapaug Pond, and West Thompson Lake) are located in the eastern part of Connecticut. The three samples with the highest mercury concentrations were from Lake Lillinonah and Lake Zoar. There appears to be a positive correlation between the concentrations of cadmium, chromium, copper, lead, nickel, zinc, and cyanide. Only 15 of the 54 synthetic organic compounds analyzed for were detected in 9 of the 12 lakes sampled. Of these 15 compounds, 14 are polycyclic aromatic hydrocarbons and the 15th is a phthalate ester. Hanover Pond had the most compounds detected (9), and phenanthrene was the compound detected in the most lakes (8).

Water-Resources Investigations Report↗
USGS1999

Concentrations and distribution of manmade organic compounds in the Lake Tahoe Basin, Nevada and California, 1997-99

The U.S. Geological Survey, in cooperation with the Tahoe Regional Planning Agency and the Lahontan Regional Water-Quality Control Board, sampled Lake Tahoe, major tributary streams to Lake Tahoe, and several other lakes in the Lake Tahoe Basin for manmade organic compounds during 1997-99. Gasoline components were found in all samples collected from Lake Tahoe during the summer boating season. Methyl tert -butyl ether (MTBE), benzene, toluene, ethylbenzene, and xylenes (BTEX) were the commonly detected compounds in these samples. Most samples from tributary streams and lakes with no motorized boating had no detectable concentrations of gasoline components. Motorized boating activity appears to be directly linked in space and time to the occurrence of these gasoline components. Other sources of gasoline components to Lake Tahoe, such as the atmosphere, surface runoff, and subsurface flow, are minor compared to the input by motorized boating. Water sampled from Lake Tahoe during mid-winter, when motorized boating activity is low, had no MTBE and only one sample had any detectable BTEX compounds. Soluble pesticides rarely were detected in water samples from the Lake Tahoe Basin. The only detectable concentrations of these compounds were in samples from Blackwood and Taylor Creeks collected during spring runoff. Concentrations found in these samples were low, in the 1 to 4 nanograms per liter range. Organochlorine compounds were detected in samples collected from semipermeable membrane devices (SPMD's) collected from Lake Tahoe, tributary streams, and Upper Angora Lake. In Lake Tahoe, SPMD samples collected offshore from urbanized areas contained the largest number and highest concentrations of organochlorine compounds. The most commonly detected organochlorine compounds were cis- and trans-chlordane, p , p' -DDE, and hexachlorobenzene. In tributary streams, SPMD samples collected during spring runoff generally had higher combined concentrations of organochlorine compounds than those collected during baseflow conditions. Upper Angora Lake had the fewest number of organochlorine compounds detected of all lake samples. Dioxins and furans were not detected in SPMD samples from two sites in Lake Tahoe or from two tributary streams. The number of polycyclic aromatic hydrocarbon (PAH) compounds and their combined concentrations generally were higher in samples from Lake Tahoe than those from tributary streams. Areas of high-motorized boating activity at Lake Tahoe had the largest number and highest concentrations of PAH's. PAH compounds were detected in samples from SPMD's in four of six tributary streams during spring runoff, all tributary streams during baseflow conditions, and at all lake sites. The most commonly detected PAH's in tributary streams during spring runoff were phenanthrene, fluoranthene, pyrene, and chrysene, and during baseflow conditions were phenanthrene, 1-methylphenanthrene, diethylnaphthalene, and pyrene. Upper Truckee River, which has an urban area in its drainage basin, had the largest number and highest combined concentration of PAH's of all stream samples. Bottom-sediment from Lake Tahoe had detectable concentrations of p-cresol, a phenol, in all but one sample. A sample collected near Chambers Lodge contained phenol at an estimated concentration of 4 micrograms per kilogram (µg/kg). Bottom-sediment samples from tributary streams had no detectable concentrations of organochlorine or PAH compounds. Several compounds were detected in bottom sediment from Upper Angora Lake at high concentrations. These compounds and their concentrations were p , p' -DDD (10 µg/kg), p , p' -DDE (7.4 µg/kg), 2,6-dimethylnaphthalene (estimated at 190 µg/kg), pentachlorophenol (3,000 µg/kg), and p-cresol (4,400 µg/kg).

California, Nevada↗
USGS2019

Organic geochemical investigation of far‐field tsunami deposits of the Kahana Valley, O'ahu, Hawai'i

Far‐field tsunami deposits observed in the Kahana Valley, O'ahu, Hawai'i (USA), were investigated for their organic‐geochemical content. During short high‐energy events, (tsunamis and storms) organic and chemical components are transported with sediment from marine to terrestrial areas. This study investigates the use of anthropogenic based organic geochemical compounds (such as polycyclic aromatic hydrocarbons, pesticides and organochlorides) as a means to identify tsunami deposits. Samples were processed by solid‐liquid extraction and analyzed using gas chromatography–mass spectrometry. A total of 21 anthropogenic marker compounds were identified, of which 11 compounds were selected for detailed analysis. Although the tsunami deposits pre‐date industrial activity in Hawaii by several hundred years, distinct changes were found in the concentrations of anthropogenic marker compounds between sandy tsunami deposits and the surrounding mud/peat layers, which may help in identifying tsunami deposits within cores. As expected, low overall concentrations of anthropogenic markers and pollutants were observed due to the lack of industrial input‐sources and little anthropogenic environmental impact at the study site. This geochemical characterization of tsunami deposits shows that anthropogenic markers have significant potential as another high‐resolution, multi‐proxy method for identifying tsunamis in the sedimentary record.

Hawai'i↗
USGS1999

Use of semipermeable membrane devices (SPMD) to assess occurrence and estimate water concentrations of selected organic compounds in the Rio Grande from Presidio to Brownsville, Texas

In Texas, the Rio Grande forms the international boundary between Mexico and the United States and extends about 2,000 kilometers from El Paso to the mouth of the Rio Grande just south of Brownsville, where the river flows into the Gulf of Mexico (fig. 1). The North American Free Trade Agreement (NAFTA) has resulted in increased industrialization and population growth on both sides of the international boundary, which in turn has focused attention on environmental issues, including water quality and quantity in the Rio Grande. Nonpoint urban and agricultural runoff and wastewater discharges from industrial and municipal facilities are potential sources of organic compounds such as polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs). Historical applications of organochlorine pesticides such as DOT and chlordane in the United States and Mexico have resulted in a continuing source of these environmentally longlived compounds in the Rio Grande Basin. In the United States, all organochlorine pesticides either have been banned entirely or have use restrictions. However, in Mexico, the organochlorine pesticide DOT is still in use, although with some application restrictions.

Fact Sheet↗
USGS2004

Gasoline-related organics in Lake Tahoe before and after prohibition of carbureted two-stroke engines

On June 1, 1999, carbureted two-stroke engines were banned on waters within the Lake Tahoe Basin of California and Nevada. The main gasoline components MTBE (methyl tert -butyl ether) and BTEX (benzene, toluene, ethylbenzene, and xylenes) were present at detectable concentrations in all samples taken from Lake Tahoe during 1997–98 prior to the ban. Samples taken from 1999 through 2001 after the ban contained between 10 and 60 percent of the pre-ban concentrations of these compounds, with MTBE exhibiting the most dramatic change (a 90 percent decrease). MTBE and BTEX concentrations in water samples from Lake Tahoe and Lower Echo Lake were related to the amount of boat use at the sampling sites. Polycyclic aromatic hydrocarbon (PAH) compounds are produced by high-temperature pyrolytic reactions. They were sampled using semipermeable membrane sampling devices in Lake Tahoe and nearby Donner Lake, where carbureted two-stroke engines are legal. PAHs were detected in all samples taken from Lake Tahoe and Donner Lake. The number of PAH compounds and their concentrations are related to boat use. The highest concentrations of PAH were detected in samples from two heavily used boating areas, Tahoe Keys Marina and Donner Lake boat ramp. Other sources of PAH, such as atmospheric deposition, wood smoke, tributary streams, and automobile exhaust do not contribute large amounts of PAH to Lake Tahoe. Similar numbers of PAH compounds and concentrations were found in Lake Tahoe before and after the ban of carbureted two-stroke engines.

California, Nevada↗
USGS2025

Potential water-quality and hydrology stressors on freshwater mussels with development of environmental DNA assays for selected mussels and macroinvertebrates in Big Darby Creek Basin, Ohio, 2020–22

The richness and abundance of freshwater mussels in the Big Darby Creek Basin has declined in recent decades, according to survey results published by the Ohio Biological Survey. In October 2016, a major mussel die-off of undetermined cause reportedly affected over 50 miles of Big Darby Creek; however, fishes and other wildlife were not noticeably impacted. Pollution, habitat destruction, climate change, and hydrologic modification have all been theorized as potential reasons for the widespread declines in freshwater mussel populations in North America. To better understand potential stressors to mussels and other aquatic organisms in the Big Darby Creek Basin, the U.S. Geological Survey, in cooperation with the Ohio Water Development Authority, evaluated water quality and temporal changes in hydrology at selected locations. In addition, environmental deoxyribonucleic acid (eDNA) quantitative polymerase chain reaction (qPCR) assays were developed to detect the presence of selected mussels and macroinvertebrates using stream water. Time-weighted average concentrations of pesticides, organic wastewater compounds (OWCs), and polycyclic aromatic hydrocarbons (PAHs) were determined for selected locations within the Big Darby Creek Basin. Passive samplers designed to mimic the respiratory exposure of aquatic organisms and the bioconcentration of organic contaminants into their fatty tissues were deployed three times annually at three sites within the Big Darby Creek Basin in 2020 and 2021. Analyses were done for 204 pesticide compounds, 38 OWCs, and 33 PAHs. Of the 204 pesticide compounds, 70 were detected in at least one sample; 30 were detected in all samples. Herbicides and herbicide degradates were the pesticides most frequently detected and also had some of the highest concentrations of the pesticides detected in this study. Three herbicides (atrazine, ametryn, and metribuzin) were detected in at least 88 percent of samples and two fungicides (azoxystrobin and propiconazole) were detected in all samples. Of the 38 OWCs, 24 were detected in at least one sample; however, only one ( N , N -diethyltoluamide [DEET]) was detected in all samples. Of the 33 PAHs, 29 were detected in at least one sample; 12 were detected in all samples. A continuous water-quality monitor was operated seasonally on Big Darby Creek above Georgesville, Ohio, from 2020 to 2022. Dissolved oxygen concentrations generally followed a daily cycle, peaking in early evening and troughing around sunrise. There were occasional 24-hour swings in dissolved oxygen concentration that had a range exceeding 10 milligrams per liter. However, dissolved oxygen concentrations never fell below Ohio’s aquatic life criteria for warmwater habitats (outside of mixing zones) of 4.0 milligrams per liter as an instantaneous minimum and 5.0 milligrams per liter as a minimum 24-hour average. The Ohio water-quality criteria for temperatures are 29.4 degrees Celsius as an instantaneous maximum and 27.8 degrees Celsius as a 24-hour average maximum. In 2020, there were 10 days when the maximum instantaneous value for temperature was exceeded and 3 consecutive days when the maximum 24-hour average temperature was exceeded. Streamflow time-series data from three gaging stations within the Big Darby Creek Basin were evaluated for trends in annual flow statistics and daily nonexceedance probabilities over time. In general, the evaluation of streamflow conditions at the Big Darby Creek gage (with 97 years of record) indicated that streamflow changed between water years 1922 and 2021. During that time span, flows in general increased, the number of high-flow pulses became more frequent, and low-flow pulses and extreme low-flow periods became less frequent. The only strong indication of trends over time in annual flow statistics for the relatively short records for the other two gages (on Little Darby Creek, with 25 years of record, and Hellbranch Run, with 29 years of record) was that as time went on, reversals between rising and falling periods became more frequent. The U.S. Geological Survey Ohio Water Microbiology Laboratory developed eDNA qPCR assays to detect Epioblasma rangiana (northern riffleshell mussels), Chimarra obscura (a species of caddisfly), Maccaffertium pulchellum (a species of mayfly), and optimized a preexisting eDNA qPCR assay to detect for Ptychobranchus fasciolaris (kidneyshell mussels). The assays were validated by using environmental sampling methods. Assay sensitivity was established by determining the limits of detection and quantification. Water samples were collected at 12 sites in the Big Darby Creek Basin between 2020 and 2022 and analyzed for eDNA with the qPCR assays developed for this study.

Ohio↗
USGS1981

Application of capillary gas chromatography mass spectrometry/computer techniques to synoptic survey of organic material in bed sediment

A bed sediment sample taken from an area impacted by heavy industrial activity was analyzed for organic compounds of environmental significance. Extraction was effected on a Soxhlet apparatus using a freeze-dried sample. The Soxhlet extract was fractionated by silica gel micro-column adsorption chromatography. Separation and identification of the organic compounds was accomplished by capillary gas chromatography/mass spectrometry techniques. More than 50 compounds were identified; these include saturated hydrocarbons, olefins, aromatic hydrocarbons, alkylated polycyclic aromatic hydrocarbons, and oxygenated compounds such as aldehydes and ketones. The role of bed sediments as a source or sink for organic pollutants is discussed.

Analytica Chimica Acta↗
USGS2007

Water-quality, sediment-quality, stream-habitat, and biological data for Mustang Bayou near Houston, Texas, 2004-05

The U.S. Geological Survey, in cooperation with the Houston-Galveston Area Council and the Texas Commission on Environmental Quality, collected water-quality, stream-habitat, and biological data from six sites (downstream order M6-M1) primarily in Brazoria County southeast of Houston, Texas, during September 2004-August 2005 and collected bed sediment data from one site in September 2005. Water-quality data collection consisted of continuously monitored (for periods of 24 hours to several days, six times) water temperature, pH, specific conductance, and dissolved oxygen and periodically collected samples of several properties and constituents. Monitored dissolved oxygen measurements were below minimum and 24-hour criteria at all sites except M2. Nitrogen compounds, phosphorus, biochemical oxygen demand, chlorophyll-a, E. coli, chloride, sulfate, solids, suspended sediment concentration, and pesticides were assessed at all sites. Concentrations of nitrogen compounds and phosphorus did not exceed Texas State screening levels. Biochemical oxygen demand was less than 4.0 milligrams per liter at all sites except M6, where the maximum concentration was 8.1 milligrams per liter. Concentrations of chlorophyll-a were less than the State screening level at all sites except M6, where four of eight samples equaled or exceeded the screening level. Twenty of 48 samples from Mustang Bayou had E. coli densities that exceeded the State single-sample water-quality standard. Median chloride concentrations from each site were between 42.2 and 123 milligrams per liter. Fifteen pesticide compounds (six herbicides and nine insecticides) were detected in 24 water samples. The most frequently detected pesticide was atrazine, which was found in every sample. Other frequently detected pesticides were 2-chloro-4-isopropylamino-6-amino-s-triazine (CIAT), prometon, tebuthiuron, fipronil, and the pesticide degradates, fipronil sulfide and fipronil sulfone. Sediment samples were collected from the stream bottom at M1 and analyzed for concentrations of trace elements (metals), polycyclic aromatic hydrocarbons, organochlorine pesticides, and polychlorinated biphenyls. No organochlorine pesticides or polychlorinated biphenyls were detected. No concentrations of metals exceeded State screening levels. Measurable concentrations of 11 polycyclic aromatic hydrocarbon (PAH) compounds were detected, and three other PAH compounds were detected but not quantified by the laboratory. Stream habitat and aquatic biota (benthic macroinvertebrates and fish) were surveyed at each site three times during the study to evaluate aquatic life use. Characteristics of habitat measured during each survey were scored using a habitat quality index. Average aquatic-life-use scores were 'limited' for M3-M6 and 'intermediate' for M1 and M2. A total of 2,557 macroinvertebrate individuals were identified from Mustang Bayou. Benthic macroinvertebrate assemblages were scored using indexes specified by the Texas Commission on Environmental Quality. Average aquatic-life-use scores were 'limited' at M1, 'intermediate' at M3-M6, and 'high' at M2. Forty-six species of fish representing 20 families were collected from Mustang Bayou. A total of 4,115 fish were collected. Sunfish (Centrarchidae) was the most abundant family, accounting for about 28 percent. Aquatic-life-use scores at sites in Mustang Bayou were determined using the regional index of biotic integrity for ecoregion 34 and were 'high' for all sites.

Data Series↗
USGS2006

Organic Compounds and Trace Elements in Fish Tissue and Bed Sediment in the Delaware River Basin, New Jersey, Pennsylvania, New York, and Delaware, 1998-2000

As part of the National Water-Quality Assessment (NAWQA) program activities in the Delaware River Basin (DELR), samples of fish tissue from 21 sites and samples of bed sediment from 35 sites were analyzed for a suite of organic compounds and trace elements. The sampling sites, within subbasins ranging in size from 11 to 600 square miles, were selected to represent 5 main land-use categories in the DELR -forest, low-agricultural, agricultural, urban, and mixed use. Samples of both fish tissue and bed sediment were also collected from 4 'large-river' sites that represented drainage areas ranging from 1,300 to 6,800 square miles, areas in which the land is used for a variety of purposes. One or more of the organochlorine compounds-DDT and chlordane metabolites, polychlorinated biphenyls (total PCBs), and dieldrin- were detected frequently in samples collected over a wide geographic area. One or more of these compounds were detected in fish-tissue samples from 92 percent of the sites and in bed-sediment samples from 82 percent of the sites. Concentrations of total DDT, total chlordanes, total PCBs, and dieldrin in whole white suckers and in bed sediment were significantly related to urban/industrial basin characteristics, such as percentage of urban land use and population density. Semi-volatile organic compounds (SVOCs)-total polycyclic aromatic hydrocarbons (PAHs), total phthalates, and phenols- were detected frequently in bed-sediment samples. All three types of SVOCs were detected in samples from at least one site in each land-use category. The highest detection rates and concentrations typically were in samples from sites in the urban and mixed land-use categories, as well as from the large-river sites. Concentrations of total PAHs and total phthalates in bed-sediment samples were found to be statistically related to percentages of urban land use and to population density in the drainage areas represented by the sampling sites. The samples of fish tissue and bed sediment collected throughout the DELR were analyzed for a large suite of trace elements, but results of the analyses for eight elements-arsenic, cadmium, chromium, copper, lead, nickel, mercury, and zinc- that are considered contaminants of concern are described in this report. One or more of the eight trace elements were detected in samples from every fish tissue and bed-sediment sampling site, and all of the trace elements were detected in samples from 97 percent of the bed-sediment sites. The concentrations of organic compounds and trace elements in the DELR samples were compared to applicable guidelines for the protection of wildlife and other biological organisms. Concentrations of total DDT, total chlordanes, total PCBs, and dieldrin in fish-tissue samples from 14 sites exceeded one or more of the Wildlife Protective Guidelines established by the New York State Department of Environmental Conservation. Concentrations of one or more organic compounds in samples from 16 bed-sediment sites exceeded the Threshold Effects Concentrations (TEC) of the Canadian Sediment Quality Guidelines, and concentrations of one or more of the eight trace elements in samples from 38 bed-sediment sites exceeded the TEC. (The TEC is the concentration below which adverse biological effects in freshwater ecosystems are expected to be rare.) Concentrations of organic compounds in samples from some bed-sediment sites exceeded the Canadian Probable Effects Concentrations (PEC), and concentrations of trace elements in samples from 18 sites exceeded the PEC. (The PEC is the concentration above which adverse effects to biological organisms are expected to occur frequently). Concentrations of organic compounds and trace elements in samples from the DELR were compared to similar data from other NAWQA study units in the northeastern United States and also data from the Mobile River (Alabama) Basin and the Northern Rockies Intermontane Basin study units. Median concentrations of to

Scientific Investigations Report↗
USGS2014

Time-integrated passive sampling as a complement to conventional point-in-time sampling for investigating drinking-water quality, McKenzie River Basin, Oregon, 2007 and 2010-11

The Eugene Water & Electric Board (EWEB) supplies drinking water to approximately 200,000 people in Eugene, Oregon. The sole source of this water is the McKenzie River, which has consistently excellent water quality relative to established drinking-water standards. To ensure that this quality is maintained as land use in the source basin changes and water demands increase, EWEB has developed a proactive management strategy that includes a combination of conventional point-in-time discrete water sampling and time‑integrated passive sampling with a combination of chemical analyses and bioassays to explore water quality and identify where vulnerabilities may lie. In this report, we present the results from six passive‑sampling deployments at six sites in the basin, including the intake and outflow from the EWEB drinking‑water treatment plant (DWTP). This is the first known use of passive samplers to investigate both the source and finished water of a municipal DWTP. Results indicate that low concentrations of several polycyclic aromatic hydrocarbons and organohalogen compounds are consistently present in source waters, and that many of these compounds are also present in finished drinking water. The nature and patterns of compounds detected suggest that land-surface runoff and atmospheric deposition act as ongoing sources of polycyclic aromatic hydrocarbons, some currently used pesticides, and several legacy organochlorine pesticides. Comparison of results from point-in-time and time-integrated sampling indicate that these two methods are complementary and, when used together, provide a clearer understanding of contaminant sources than either method alone.

Oregon↗
USGS2014

Organic substances in produced and formation water from unconventional natural gas extraction in coal and shale

Organic substances in produced and formation water from coalbed methane (CBM) and gas shale plays from across the USA were examined in this study. Disposal of produced waters from gas extraction in coal and shale is an important environmental issue because of the large volumes of water involved and the variable quality of this water. Organic substances in produced water may be environmentally relevant as pollutants, but have been little studied. Results from five CBM plays and two gas shale plays (including the Marcellus Shale) show a myriad of organic chemicals present in the produced and formation water. Organic compound classes present in produced and formation water in CBM plays include: polycyclic aromatic hydrocarbons (PAHs), heterocyclic compounds, alkyl phenols, aromatic amines, alkyl aromatics (alkyl benzenes, alkyl biphenyls), long-chain fatty acids, and aliphatic hydrocarbons. Concentrations of individual compounds range from < 1 to 100 μg/L, but total PAHs (the dominant compound class for most CBM samples) range from 50 to 100 μg/L. Total dissolved organic carbon (TOC) in CBM produced water is generally in the 1–4 mg/L range. Excursions from this general pattern in produced waters from individual wells arise from contaminants introduced by production activities (oils, grease, adhesives, etc.). Organic substances in produced and formation water from gas shale unimpacted by production chemicals have a similar range of compound classes as CBM produced water, and TOC levels of about 8 mg/L. However, produced water from the Marcellus Shale using hydraulic fracturing has TOC levels as high as 5500 mg/L and a range of added organic chemicals including, solvents, biocides, scale inhibitors, and other organic chemicals at levels of 1000 s of μg/L for individual compounds. Levels of these hydraulic fracturing chemicals and TOC decrease rapidly over the first 20 days of water recovery and some level of residual organic contaminants remain up to 250 days after hydraulic fracturing. Although the environmental impacts of the organics in produced water are not well defined, results suggest that care should be exercised in the disposal and release of produced waters containing these organic substances into the environment because of the potential toxicity of many of these substances.

International Journal of Coal Geology↗
USGS2017

Influence of sediment chemistry and sediment toxicity on macroinvertebrate communities across 99 wadable streams of the Midwestern USA

Simultaneous assessment of sediment chemistry, sediment toxicity, and macroinvertebrate communities can provide multiple lines of evidence when investigating relations between sediment contaminants and ecological degradation. These three measures were evaluated at 99 wadable stream sites across 11 states in the Midwestern United States during the summer of 2013 to assess sediment pollution across a large agricultural landscape. This evaluation considers an extensive suite of sediment chemistry totaling 274 analytes (polycyclic aromatic hydrocarbons, organochlorine compounds, polychlorinated biphenyls, polybrominated diphenyl ethers, trace elements, and current-use pesticides) and a mixture assessment based on the ratios of detected compounds to available effects-based benchmarks. The sediments were tested for toxicity with the amphipod Hyalella azteca (28-d exposure), the midge Chironomus dilutus (10-d), and, at a few sites, with the freshwater mussel Lampsilis siliquoidea (28-d). Sediment concentrations, normalized to organic carbon content, infrequently exceeded benchmarks for aquatic health, which was generally consistent with low rates of observed toxicity. However, the benchmark-based mixture score and the pyrethroid insecticide bifenthrin were significantly related to observed sediment toxicity. The sediment mixture score and bifenthrin were also significant predictors of the upper limits of several univariate measures of the macroinvertebrate community (EPT percent, MMI (Macroinvertebrate Multimetric Index) Score, Ephemeroptera and Trichoptera richness) using quantile regression. Multivariate pattern matching (Mantel-like tests) of macroinvertebrate species per site to identified contaminant metrics and sediment toxicity also indicate that the sediment mixture score and bifenthrin have weak, albeit significant, influence on the observed invertebrate community composition. Together, these three lines of evidence (toxicity tests, univariate metrics, and multivariate community analysis) suggest that elevated contaminant concentrations in sediments, in particular bifenthrin, is limiting macroinvertebrate communities in several of these Midwest streams.

Science of the Total Environment↗