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Michael T. Meyer

Publications and source records attributed to Michael T. Meyer.

At least 73 records · Page 4Linked to original sources
USGS2007

Effects of sorbate speciation on sorption of selected sulfonamides in three loamy soils

Sorption of sulfamethazine (SMN) and sulfathiazole (STZ) was investigated in three soils, a North Carolina loamy sand, an Iowa sandy loam, and a Missouri loam, under various pH conditions. A significant increase in the sorption coefficient ( K D ) was observed in all three soils, as the sulfonamides converted from an anionic form at higher pH to a neutral/cationic form at lower pH. Above pH 7.5, sulfonamides exist primarily in anionic form and have higher aqueous solubility and no cationic character, thereby consequently leading to lower sorption to soils. The effect of speciation on sorption is not the same for all sulfonamides; it is a function of the pH of the soil and the p K a of the sulfonamides. The results indicate that, for the soils under investigation, SMN has comparatively lower K D values than STZ. The pH-dependent sorption of sulfonamides was observed to be consistent in all three soils investigated. The K D values for each speciated form cationic, neutral, and anionic were calculated using an empirical model in which the species-specific sorption coefficients ( K D0 , K D1 , and K D2 ) were weighted with their respective fractions present at any given pH.

Journal of Agricultural and Food Chemistry↗
USGS2007

Efficiency of conventional drinking-water-treatment processes in removal of pharmaceuticals and other organic compounds

Samples of water and sediment from a conventional drinking-water-treatment (DWT) plant were analyzed for 113 organic compounds (OCs) that included pharmaceuticals, detergent degradates, flame retardants and plasticizers, polycyclic aromatic hydrocarbons (PAHs), fragrances and flavorants, pesticides and an insect repellent, and plant and animal steroids. 45 of these compounds were detected in samples of source water and 34 were detected in samples of settled sludge and (or) filter-backwash sediments. The average percent removal of these compounds was calculated from their average concentration in time-composited water samples collected after clarification, disinfection (chlorination), and granular-activated-carbon (GAC) filtration. In general, GAC filtration accounted for 53% of the removal of these compounds from the aqueous phase; disinfection accounted for 32%, and clarification accounted for 15%. The effectiveness of these treatments varied widely within and among classes of compounds; some hydrophobic compounds were strongly oxidized by free chlorine, and some hydrophilic compounds were partly removed through adsorption processes. The detection of 21 of the compounds in 1 or more samples of finished water, and of 3 to 13 compounds in every finished-water sample, indicates substantial but incomplete degradation or removal of OCs through the conventional DWT process used at this plant.

Science of the Total Environment↗
USGS2007

Concentrations of selected pharmaceuticals and antibiotics in south-central Pennsylvania waters, March through September 2006

This report presents environmental and quality-control data from analyses of 15 pharmaceutical and 31 antibiotic compounds in water samples from streams and wells in south-central Pennsylvania. The analyses are part of a study by the U.S. Geological Survey (USGS) in cooperation with the Pennsylvania Department of Environmental Protection (PADEP) to define concentrations of selected emerging contaminants in streams and well water in Pennsylvania. Sampling was conducted at 11 stream sites and at 6 wells in 9 counties of south-central Pennsylvania. Five of the streams received municipal wastewater and 6 of the streams received runoff from agricultural areas dominated by animal-feeding operations. For all 11 streams, samples were collected at locations upstream and downstream of the municipal effluents or animal-feeding operations. All six wells were in agricultural settings. A total of 120 environmental samples and 21 quality-control samples were analyzed for the study. Samples were collected at each site in March/April, May, July, and September 2006 to obtain information on changes in concentration that could be related to seasonal use of compounds. For streams, 13 pharmaceuticals and 11 antibiotics were detected at least 1 time. Detections included analytical results that were estimated or above the minimum reporting limits. Seventy-eight percent of all detections were analyzed in samples collected downstream from municipal-wastewater effluents. For streams receiving wastewater effluents, the pharmaceuticals caffeine and para-xanthine (a degradation product of caffeine) had the greatest concentrations, 4.75 μg/L (micrograms per liter) and 0.853 μg/L, respectively. Other pharmaceuticals and their respective maximum concentrations were carbamazepine (0.516 μg/L) and ibuprofen (0.277 μg/L). For streams receiving wastewater effluents, the antibiotic azithromycin had the greatest concentration (1.65 μg/L), followed by sulfamethoxazole (1.34 μg/L), ofloxacin (0.329 μg/L), and trimethoprim (0.256 μg/L). For streams receiving runoff from animal-feeding operations, the only pharmaceuticals detected were acetaminophen, caffeine, cotinine, diphenhydramine, and carbamazepine. The maximum concentration for pharmaceuticals was 0.053 μg/L. Three streams receiving runoff from animal-feeding operations had detections of one or more antibiotic compound--oxytetracycline, sulfadimethoxine, sulfamethoxazole, and tylosin. The maximum concentration for antibiotics was 0.157 μg/L. The average number of compounds (pharmaceuticals and antibiotics) detected in sites downstream from animal-feeding operations was three. The average number of compounds detected downstream from municipal-wastewater effluents was 13. For wells used to supply livestock, four compounds were detected--two pharmaceuticals (cotinine and diphenhydramine) and two antibiotics (tylosin and sulfamethoxazole). There were five detections in all the well samples. The maximum concentration detected in well water was for cotinine, estimated to be 0.024 μg/L. Seasonal occurrence of pharmaceutical and antibiotic compounds in stream water varied by compound and site type. At four stream sites, the same compounds were detected in all four seasonal samples. At other sites, pharmaceutical or antibiotic compounds were detected only one time in seasonal samples. Winter samples collected in streams receiving municipalwastewater effluent had the greatest number of compounds detected (21). Research analytical methods were used to determine concentrations for pharmaceuticals and antibiotics. To assist in evaluating the quality of the analyses, detailed information is presented on laboratory methodology and results from qualitycontrol samples. Quality-control data include results for nine blanks, nine duplicate environmental sample pairs, and three laboratory-spiked environmental samples as well as the recoveries of compounds in laboratory surrogates and laboratory reagent spikes.

Pennsylvania↗
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↗
USGS2007

Occurrence of selected pharmaceuticals, personal-care products, organic wastewater compounds, and pesticides in the lower Tallapoosa River watershed near Montgomery, Alabama, 2005

Synthetic and natural organic compounds derived from agricultural operations, residential development, and treated and untreated sanitary and industrial wastewater discharges can contribute contaminants to surface and ground waters. To determine the occurrence of these compounds in the lower Tallapoosa River watershed, Alabama, new laboratory methods were used that can detect human and veterinary antibiotics; pharmaceuticals; and compounds found in personal-care products, food additives, detergents and their metabolites, plasticizers, and other industrial and household products in the environment. Well-established methods for detecting 47 pesticides and 19 pesticide degradates also were used. In all, 186 different compounds were analyzed by using four analytical methods. The lower Tallapoosa River serves as the water-supply source for more than 100,000 customers of the Montgomery Water Works and Sanitary Sewer Board. Source-water protection is a high priority for the Board, which is responsible for providing safe drinking water. The U.S. Geological Survey, in cooperation with the Montgomery Water Works and Sanitary Sewer Board, conducted this study to provide baseline data that could be used to assess the effects of agriculture and residential development on the occurrence of selected organic compounds in the lower Tallapoosa River watershed. Twenty samples were collected at 10 sites on the Tallapoosa River and its tributaries. Ten samples were collected in April 2005 during high base streamflow, and 10 samples were collected in October 2005 when base streamflow was low. Thirty-two of 186 compounds were detected in the lower Tallapoosa River watershed. Thirteen compounds, including atrazine, 2-chloro-4-isopropylamino-6-amino-s-triazine (CIAT), hexazinone, metalaxyl, metolachlor, prometryn, prometon, simazine, azithromycin, oxytetracycline, sulfamethoxazole, trimethoprim, and tylosin, had measurable concentrations above their laboratory reporting levels. Concentrations were estimated for an additional 19 compounds that were detected below their laboratory reporting levels. The two most frequently detected compounds were the pesticides atrazine (19 of 20 samples) and simazine (13 of 20 samples). Tylosin, a veterinary antibiotic, was detected in 8 of 20 samples. Other compounds frequently detected at very low concentrations included CIAT and hexazinone (a degradate of atrazine and a pesticide, respectively); camphor (derived from personal-care products or flavorants), para-cresol (various uses including solvent, wood preservative, and in household cleaning products), and N,N-diethyl-m-toluamide (DEET, an insect repellent).

Alabama↗
USGS2007

Methods of analysis by the U.S. Geological Survey Organic Geochemistry Research Group--Determination of dissolved isoxaflutole and its sequential degradation products, diketonitrile and benzoic acid, in water using solid-phase extraction and liquid chromatography/tandem mass spectrometry

An analytical method for the determination of isoxaflutole and its sequential degradation products, diketonitrile and a benzoic acid analogue, in filtered water with varying matrices was developed by the U.S. Geological Survey Organic Geochemistry Research Group in Lawrence, Kansas. Four different water-sample matrices fortified at 0.02 and 0.10 ug/L (micrograms per liter) are extracted by vacuum manifold solid-phase extraction and analyzed by liquid chromatography/tandem mass spectrometry using electrospray ionization in negative-ion mode with multiple-reaction monitoring (MRM). Analytical conditions for mass spectrometry detection are optimized, and quantitation is carried out using the following MRM molecular-hydrogen (precursor) ion and product (p) ion transition pairs: 357.9 (precursor), 78.9 (p), and 277.6 (p) for isoxaflutole and diketonitrile, and 267.0 (precursor), 159.0 (p), and 223.1 (p) for benzoic acid. 2,4-dichlorophenoxyacetic acid-d3 is used as the internal standard, and alachlor ethanesulfonic acid-d5 is used as the surrogate standard. Compound detection limits and reporting levels are calculated using U.S. Environmental Protection Agency procedures. The mean solid-phase extraction recovery values ranged from 104 to 108 percent with relative standard deviation percentages ranging from 4.0 to 10.6 percent. The combined mean percentage concentration normalized to the theoretical spiked concentration of four water matrices analyzed eight times at 0.02 and 0.10 ug/L (seven times for the reagent-water matrix at 0.02 ug/L) ranged from approximately 75 to 101 percent with relative standard deviation percentages ranging from approximately 3 to 26 percent for isoxaflutole, diketonitrile, and benzoic acid. The method detection limit (MDL) for isoxaflutole and diketonitrile is 0.003 ug/L and 0.004 ug/L for benzoic acid. Method reporting levels (MRLs) are 0.011, 0.010, and 0.012 ug/L for isoxaflutole, diketonitrile, and benzoic acid, respectively. On the basis of the calculated MRLs and MDLs and evaluation of the signal-to-noise ratios for each compound, the MRLs and MDLs are set at 0.010 and 0.003 ug/L, respectively, for all three compounds.

Techniques and Methods↗
USGS2006

A global perspective on the use, sales, exposure pathways, occurrence, fate and effects of veterinary antibiotics (VAs) in the environment

Veterinary antibiotics (VAs) are widely used in many countries worldwide to treat disease and protect the health of animals. They are also incorporated into animal feed to improve growth rate and feed efficiency. As antibiotics are poorly adsorbed in the gut of the animals, the majority is excreted unchanged in faeces and urine. Given that land application of animal waste as a supplement to fertilizer is often a common practice in many countries, there is a growing international concern about the potential impact of antibiotic residues on the environment. Frequent use of antibiotics has also raised concerns about increased antibiotic resistance of microorganisms. We have attempted in this paper to summarize the latest information available in the literature on the use, sales, exposure pathways, environmental occurrence, fate and effects of veterinary antibiotics in animal agriculture. The review has focused on four important groups of antibiotics (tylosin, tetracycline, sulfonamides and, to a lesser extent, bacitracin) giving a background on their chemical nature, fate processes, occurrence, and effects on plants, soil organisms and bacterial community. Recognising the importance and the growing debate, the issue of antibiotic resistance due to the frequent use of antibiotics in food-producing animals is also briefly covered. The final section highlights some unresolved questions and presents a way forward on issues requiring urgent attention.

Chemosphere↗
USGS2006

Response to comment on “Persistence of pharmaceutical compounds and other organic wastewater contaminants in a conventional drinking-water-treatment plant”

The U.S. Geological Survey (USGS) and the Centers for Disease Control thank Dr. Till for her comments concerning our research ( Till, 2005 ) and welcome the opportunity to respond. The primary objective of our study was to evaluate the potential for organic wastewater-related contaminants (OWCs), including pharmaceuticals, to survive a conventional drinking-water-treatment process and persist in potable-water supplies ( Stackelberg et al., 2004 ). Our study was supported by two USGS laboratories: the National Water Quality Laboratory (NWQL), which provided the HPLC/ESI-MS and CLLE GC/MS data and the Ocala Water Quality and Research Laboratory (OWQRL), which provided the LC/MS data ( Stackelberg et al., 2004 ). Although discussed as distinct techniques by Dr. Till and indicated by differing acronyms to distinguish the laboratories producing the data, as described in our paper, the two LC/MS methods are very similar; they consist of a solid-phase extraction method with analysis of the extract produced using high-performance liquid chromatography coupled to an electrospray ionization mass spectrometer operated in the positive mode. The NWQL and OWQRL report ‘trace’ and ‘ultratrace’ determinations of analytes that provide significant benefit for describing the presence and fate of low-level contaminants. For mass spectral methods, an analyte is qualitatively identified by its retention time on the chromatographic column as well as the presence of two or more confirming ions with area ratios that match that of the reference standard compounds. Because of a recognized increased risk of false positives, these qualitative identification criteria are used in conjunction with abundant quality-control samples (detailed below) to confirm detection prior to making an estimate of the concentration. These qualitative identification criteria must be met before a compound is considered present (or detected) in a sample ( Oblinger Childress et al., 1999 ). When a compound has been qualitatively identified in an environmental sample (whether above or below its reporting level [RL]), it is assessed in context with associated field and laboratory blanks, field and laboratory replicates, and other data, such as appropriate laboratory reagent spikes. An environmental concentration is calculated only after determining that field and laboratory procedures did not contaminate the samples. The concentrations are then calculated from 5- to 8-point calibration curves using internal standard quantitation. Our lowest calibration standard is intentionally much lower than the RL, typically 10 times lower. The most abundant molecular or fragment ion is used for quantitation, and, for the two LC/MS methods, at least one, and where possible two, qualifier ions are used for confirmation. For the GC/MS method, with its greater degree of fragmentation, one quantitation and two qualifier ions are used. When any of the abovementioned qualitative identification criteria are not met, the analyte is considered not present and is reported as “less than” the RL.

Science of the Total Environment↗
USGS2006

Results of analyses of the fungicide Chlorothalonil, its degradation products, and other selected pesticides at 22 surface-water sites in five Southern states, 2003-04

In accordance with the mission of the U.S. Geological Survey (USGS) Toxic Substances Hydrology Program, a pesticide study was conducted during 2003–04 to determine the occurrence of the fungicide chlorothalonil and its degradation products at 22 surface-water sites in five Southern States. Water-quality samples were collected during the peanut-growing season (June–September) in 2003. During the peanut-growing season in 2004, samples were collected after large storms. An analytical method was developed at the USGS Organic Geochemistry Research Laboratory in Lawrence, Kansas, to measure chlorothalonil and its degradation products by liquid chromatography/mass spectrometry (LC/MS). Chlorothalonil was detected in 4 of the 113 surface-water samples. The primary degradation product of chlorothalonil, 4-hydroxy-chlorothalonil, was detected in 26 of the 113 samples with concentrations ranging from 0.002 to 0.930 microgram per liter. The chlorothalonil degradation products, 1-amide-4-hydroxy-chorothalonil and 1,3-diamide-chlorothalonil, were detected in one water sample each at 0.020 and 0.161 microgram per liter, respectively. The USGS Methods and Research Development Group, Lakewood, Colorado, developed a custom method for chlorothalonil using gas chromatography/mass spectrometry (GC/MS) in an effort to achieve a lower laboratory reporting level (LRL) than the USGS National Water-Quality Laboratory (NWQL) schedule 2060, which analyzes the compound chlorothalonil at a LRL of 0.035 µg/L. The group succeeded in achieving a lower GC/MS reporting level of 0.01 µg/L. Chlorothalonil was detected in 5 of 68 water samples analyzed using the custom GC/MS method, whereas chlorothalonil was detected in 2 of 21 water samples analyzed using NWQL schedule 2060. In addition to analysis of chlorothalonil and its degradation products, samples were analyzed using the USGS NWQL schedules 2001 and 2060 for about 114 pesticides and their degradation products. Samples also were analyzed for dissolved organic carbon, suspended sediment, and percentage of silt- and clay-sized particles. Overall, it was found that chlorothalonil was detected only infrequently and at relatively low concentrations. Chlorothalonil’s major degradation product, 4-hydroxy-chlorothalonil, was detected most frequently, occurred generally at higher concentrations in water samples than did the parent fungicide, and the data from this study reaffirmed that it is the dominant degradation product of chlorothalonil in the peanut-growing environment.

Open-File Report↗
USGS2006

Occurrence of organic wastewater compounds in drinking water, wastewater effluent, and the Big Sioux River in or near Sioux Falls, South Dakota, 2001-2004

The U.S. Geological Survey (USGS) in cooperation with the city of Sioux Falls conducted several rounds of sampling to determine the occurrence of organic wastewater compounds (OWCs) in the city of Sioux Falls drinking water and waste-water effluent, and the Big Sioux River in or near Sioux Falls during August 2001 through May 2004. Water samples were collected during both base-flow and storm-runoff conditions. Water samples were collected at 8 sites, which included 4 sites upstream from the wastewater treatment plant (WWTP) discharge, 2 sites downstream from the WWTP discharge, 1 finished drinking-water site, and 1 WWTP effluent (WWE) site. A total of 125 different OWCs were analyzed for in this study using five different analytical methods. Analyses for OWCs were performed at USGS laboratories that are developing and/or refining small-concentration (less than 1 microgram per liter (ug/L)) analytical methods. The OWCs 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). Some of the compounds in the HPC, MAH, HIAC, and PAH classes are suspected of being endocrine-disrupting compounds (EDCs). Of the 125 different OWCs analyzed for in this study, 81 OWCs had one or more detections in environmental samples reported by the laboratories, and of those 81 OWCs, 63 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 drinking water, wastewater effluent, and the Big Sioux River. OWCs in all compound classes were detected in water samples from sampling sites in the Sioux Falls area. For the five sampling periods when samples were collected from the Sioux Falls finished drinking water, only one OWC was detected at a concentration greater than the study reporting level (metolachlor; 0.0040 ug/L). During base-flow conditions, Big Sioux River sites upstream from the WWTP discharge had OWC contributions that primarily were from nonpoint animal or crop agriculture sources or had OWC concentrations that were minimal. The influence of the WWTP discharge on OWCs at downstream river sites during base-flow conditions ranged from minimal influence to substantial influence depending on the sampling period. During runoff conditions, OWCs at sites upstream from the WWTP discharge probably were primarily contributed by nonpoint animal and/or crop agriculture sources and possibly by stormwater runoff from nearby roads. OWCs at sites downstream from the WWTP discharge probably were contributed by sources other than the WWTP effluent discharge, such as stormwater runoff from urban and/or agriculture areas and/or resuspension of OWCs adsorbed to sediment deposited in the Big Sioux River. OWC loads generally were substantially smaller for upstream sites than downstream sites during both base-flow and runoff conditions.discharge had OWC contributions that primarily were from nonpoint animal or crop agriculture sources or had OWC concentrations that were minimal. The influence of the WWTP discharge on OWCs at downstream river sites during base-flow conditions ranged from minimal influence to substantial influence depending on the sampling period. During runoff conditions, OWCs at sites upstream from the WWTP discharge probably were primarily contributed by nonpoint animal and/or crop agriculture sources and possibly by stormwater runoff from nearby roads. OWCs at sites downstream from the WWTP discharge probably were contributed by sources other than the WWTP effluent discharge, such as stormwater runoff from urban and/or agriculture areas and/or resuspension of OWCs adsorbed to sediment deposited in the Big Sioux River. OWC loads generally were substantially smaller for

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↗
USGS2006

Evaluation of emerging contaminants of concern at the South District Wastewater Treatment Plant based on seasonal sampling events, Miami-Dade County, Florida, 2004

The Comprehensive Everglades Restoration Plan has identified highly treated wastewater as a possible water source for the restoration of natural water flows and hydroperiods in selected coastal areas, including the Biscayne Bay coastal wetlands. One potential source of reclaimed wastewater for the Biscayne Bay coastal wetlands is the effluent from the South District Wastewater Treatment Plant in southern Miami-Dade County. The U.S. Geological Survey, in cooperation with the Comprehensive Everglades Restoration Plan Wastewater Reuse Technology Pilot Project Delivery Team, initiated a study to assess the presence of emerging contaminants of concern in the South District Wastewater Treatment Plant influent and effluent using current wastewater-treatment methods. As part of the study, 24-hour composite and discrete samples were collected at six locations (influent at plants 1 and 2, effluent pump, reuse train, chlorine dioxide unit, and ultraviolet pilot unit) at the plant during: (1) a dry-season, low-flow event on March 2-3, 2004, with an average inflow rate of 83.7 million gallons per day; (2) a wet-season, average-flow event on July 20-21, 2004, with an average inflow rate of 89.7 million gallons per day; and (3) high-rate disinfection tests on October 5 and 20, 2004, with average flow rates of 84.1 and 119.6 million gallons per day, respectively. During these four sampling events, 26, 27, 29, and 35 constituents were detected, respectively. The following transformations in concentration were determined in the waste stream: -100 to 180 percent at the effluent pump and -100 to 85 percent at the reuse train on March 2-3, 2004, and -100 to 1,609 percent at the effluent pump and -100 to 832 percent at the reuse train on July 20-21, 2004; -100 to -37 percent at the effluent pump, -100 to -62 percent at the reuse train, -100 to -56 percent at the chlorine dioxide unit, and -100 to -40 percent at the ultraviolet pilot unit on October 5, 2004; and -100 to -4 percent at the effluent pump, -100 to 17 percent at the reuse train, -100 to -40 percent at the chlorine dioxide unit, and -100 to -14 percent at the ultraviolet pilot unit on October 20, 2004. Samples were tested for detection of household and industrial (organic) wastewater compounds, pharmaceutical compounds, antibiotic compounds, and hormones in influent. Two 'known' endocrine disrupting compounds?17 beta-estradiol (E2) and diethoxynonylphenol? and four 'suspected' endocrine-disrupting compounds?1,4-dichlorobenzene, benzophenone, tris(2-chloroethyl) phosphate, and tris(dichloroisopropyl) phosphate?were detected during these sampling events. Phenanthrene and indole showed the greatest concentration ranges and highest concentrations for the organic wastewater compounds. Acetaminophen showed the greatest concentration range and highest concentration, and warfarin showed the smallest concentration range for the pharmaceutical compounds. Sulfamethoxazole (a sulfonamide) showed the greatest concentration range and highest concentration, and sulfathiozole (also a sulfonamide) showed the smallest concentration range for the antibiotic compounds. Two hormones, 17 beta-estradiol (E2) and estrone (E1), were detected in influent. Samples were also tested for detection of organic wastewater compounds, pharmaceutical compounds, antibiotic compounds, and hormones in effluent. Indole showed the greatest concentration range and highest concentration, and triphenyl phosphate showed the smallest concentration range for the organic wastewater compounds. Dehydronifedipine showed the greatest concentration range and highest concentration, and warfarin had the smallest concentration range for the pharmaceutical compounds. Anhydro-erythromycin (a macrolide degradation product) showed the greatest concentration range, and sulfadiazine (a sulfonamide) and tetracycline showed the lowest concentration ranges for the antibiotic compounds. One hormone, 17 beta-estradiol (E2), was det

Florida↗
USGS2006

Occurrence and transport of agricultural chemicals in Leary Weber Ditch Basin, Hancock County, Indiana, 2003-04

Leary Weber Ditch Basin, Hancock County, Indiana, is one of seven first-order basins selected from across the United States as part of the Agricultural Chemicals: Source, Transport, and Fate study conducted by the National Water-Quality Assessment Program of the U.S. Geological Survey. The nationwide study was designed to increase the understanding of the links between the sources of water and agricultural chemicals (nutrients and pesticides) and the transport and fate of these chemicals through the environment. Agricultural chemicals were detected in Leary Weber Ditch and in every associated hydrologic compartment sampled during 2003 and 2004. Pesticides were detected more frequently in samples collected from overland flow and from the ditch itself and less frequently in ground-water samples. The lowest concentrations of pesticides and nutrients were detected in samples of rain, soil water, and ground water. The highest concentrations of pesticides and nutrients were detected in samples of tile-drain water, overland flow, and water from Leary Weber Ditch. Samples collected from the tile drain, overland flow and Leary Weber Ditch soon after chemical applications to the fields and coincident with rainfall and increased streamflow had higher concentrations of pesticides and nutrients than samples collected a longer time after the chemicals were applied. A mass-balance mixing analysis based on potassium concentrations indicated that tile drains are the primary contributor of water to Leary Weber Ditch, but overland flow is also an important contributor during periods of high-intensity rainfall. When maximum rainfall intensity was 0.5 inches per hour or lower, overland flow contributed about 10 percent and tile drains contributed about 90 percent of the flow to Leary Weber Ditch. When maximum rainfall intensity was 0.75 inches per hour or greater, overland flow contributed about 40 percent and tile drains contributed about 60 percent of the flow to the ditch. Ground-water flow to Leary Weber Ditch was negligible. Tile drains are an important agricultural-chemical transport path to Leary Weber Ditch, based on the hydrologic contributions of overland flow and tile drains to the ditch. Overland flow is also an important agricultural-chemical transport pathway during high-intensity rainfall; however, storms with high-intensity rainfall are sporadic throughout the year. Tile drains and the soil water moving to the tile drains are the primary transport pathway for agricultural-chemical transport to Leary Weber Ditch during most storms as well as between storms.

Indiana↗
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

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↗
USGS2005

Studies examine contaminants: Pharmaceuticals, hormones and other organic wastewater contaminants in ground water resources

Ground water provides approximately 40 percent of the nation’s public water supply, and the total percentage of withdrawals for irrigation has increased from 23 percent in 1950 to 42 percent in 2000. Ground water also is a major contributor to flow in many streams and rivers in the United States and has a substantial influence on river and wetland habitats for plants and animals. Organic wastewater contaminants (OWCs) in the environment recently have been documented to be of global concern with a variety of sources and source pathways.

National Driller↗